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Sample records for alcoholic carbonate solution

  1. Carbonized properties of iodine-incorporated poly(vinyl alcohol) composite films prepared by gelation/crystallization from solution.

    PubMed

    Nakano, Yumiko; Matsuo, Masaru

    2010-02-16

    Poly(vinyl alcohol) (PVA) and titanium dioxide (TiO(2)) composite films were prepared by gelation/crystallization from a dispersed solution containing different TiO(2) contents against PVA. Iodine was incorporated into the composites, and the iodine-incorporated composites were carbonized under argon gas in the temperature range of 700-1600 degrees C. Under the carbonization process, the incorporation of iodine into composites ensured tough films without cracks. This indicated that iodine incorporation played an important role as a catalyst to promote the formation of cross links between amorphous carbon chains through the resultant Ti-C structure that occurs by hydration. Surprisingly, X-ray diffraction intensity measurements revealed that the coagulated TiO(2) powders in the composite film carbonized at 1200 degrees C remained predominantly anatase type, which has generally been known as photocatalytic activity. The perfect transition to the rutile-type structure dramatically occurred at 1600 degrees C. Judging from the carbon coating on the TiO(2) particle surface as detected by ESCA, no disruption of the composite was found to be due to the appearances of Ti(2)O(3) groups and the Ti-C structure performing cross linking between neighboring amorphous carbon chains. The characteristics of anatase-type TiO(2) crystallites and amorphous carbon structures were analyzed using the para-crystalline theory concerning the distance fluctuation between graphene sheets. The electrical conductivity of the carbonized composite was ca. 0.01 S/cm and was independent of the TiO(2) admixed in the carbon matrix. PMID:19883066

  2. Photoinduced crystallization of calcium carbonate from a homogeneous precursor solution in the presence of partially hydrolyzed poly(vinyl alcohol)

    NASA Astrophysics Data System (ADS)

    Nishio, Takashi; Naka, Kensuke

    2015-04-01

    Photoinduced crystallization of calcium carbonate (CaCO3) was demonstrated by the photodecarboxylation of ketoprofen (KP, 2-(3-benzoylphenyl)propionic acid) under alkaline conditions (pH 10). In this method, a homogeneous solution comprising KP, calcium chloride, ammonia, and partially hydrolyzed poly(vinyl alcohol) (PVAPS, degree of saponification: 86.5-89.0 mol %) was used as the precursor solution and was exposed to ultraviolet (UV) irradiation for different time periods. Thermogravimetric analysis of the obtained xerogels showed that increasing the UV irradiation time increased the amount of CaCO3 formed and the complete conversion of calcium ions to calcite was achieved after 50 min of UV irradiation. Furthermore, solid phase analyses suggested that nanometer-to-micron-sized calcite crystals were formed and dispersed in the obtained PVAPS matrix.

  3. Solution thermodynamics for alkoxy phenols in alcohol and in water-alcohol systems

    SciTech Connect

    Beezer, A.E.; Hunter, W.H.; Lima, M.C.P.; Volpe, P.L.O.

    1986-04-01

    Solubilities have been measured for m-alkoxyphenols in water-alcohol mixtures. The alcohols ranged from the co-solvent methanol to the co-solute 1-octanol, and each alcohol was present at the saturating concentration of 1-octanol in water viz. 0.00316M. Plots of solubility vs. carbon number of the alcohols show discontinuities. Enthalpies of solution in these same solvent systems have also been measured. The enthalpies of solution and the derived enthalpies of transfer both support the observations on solubilities. The results are discussed on the basis of solvent-solute interactions and in terms of solute volumes.

  4. Extracting alcohols from aqueous solutions. [USDOE patent application

    DOEpatents

    Compere, A.L.; Googin, J.M.; Griffith, W.L.

    1981-12-02

    The objective is to provide an efficient process for extracting alcohols in aqueous solutions into hydrocarbon fuel mixtures, such as gasoline, diesel fuel and fuel oil. This is done by contacting an aqueous fermentation liquor with a hydrocarbon or hydrocarbon mixture containing carbon compounds having 5-18 carbon atoms, which may include gasoline, diesel fuel or fuel oil. The hydrocarbon-aqueous alcohol solution is then mixed with one or more of a group of polyoxyalkylene polymers to extract the alcohol into the hydrocarbon fuel-polyoxyalkylene polymer mixture.

  5. Pervaporation separation of aqueous alcohol solution through asymmetric polycarbonate membrane

    SciTech Connect

    Lee, K.R.; Liu, M.J.; Lai, J.Y. )

    1994-01-01

    In the present work the separation of aqueous alcohol mixtures through wet-phase inversion prepared polycarbonate membranes was studied by using the pervaporation process. The formation of asymmetric pervaporation membranes was discussed in terms of the presence of a nonsolvent in the casting solution, the polycarbonate concentration, and the kinds of coagulation media. The effects of feed composition, swelling degree, and the size of the alcohols on the pervaporation performances were investigated. The rate of liquid-liquid demixing increases with a decreasing number of carbon atoms of the alcohol coagulation medium. The permeation rate of the pervaporation process for the nonsolvent-added membrane was much higher than that of the membrane without nonsolvent additive. In binary alcohol mixtures, the permselectivities of small-sized alcohols through the asymmetric membrane are decided by two factors: preferential solubility of larger-sized alcohol and predominant diffusivity of small-sized alcohol. 19 refs., 8 figs., 6 tabs.

  6. Polycondensation kinetics of furfuryl alcohol solutions

    NASA Astrophysics Data System (ADS)

    Zherebtsov, D. A.; Galimov, D. M.; Zagorul'ko, O. V.; Frolova, E. V.; Bol'shakov, O. I.; Zakharov, V. G.; Mikhailov, G. G.

    2016-01-01

    Changes in the viscosity, electrical conductivity, monomer concentration, and the size of growing molecules of polycondensed furfuryl alcohol are studied in solutions containing triethylene glycol and isooctylphenyldecaethylene glycol. The effect the solution compositions have on the condensation kinetics is considered.

  7. Time and Temperature Dependent Rheological Behavior of Single-Walled Carbon Nanotubes Dispersed in Thermoreversible Acrylic Copolymer & Alcohol Solutions

    NASA Astrophysics Data System (ADS)

    Schoch, Andrew B.; Shull, Kenneth R.; Brinson, L. Catherine

    2008-03-01

    SWCNT stabilized by A-B diblock and A-B-A triblock copolymers are excellent model systems for studying the relationship between nanotube dispersion and mechanical response. We have investigated the mechanical properties of these materials with low-amplitude oscillatory shear rheological measurements. The solvent used here, 2-ethyl-1-hexanol, is a poor solvent for PMMA (A) at low temperatures but a good solvent for PnBA (B) over the entire temperature range studied. The solubility of the PMMA blocks in 2-ethyl-1-hexanol drives the formation of an elastic gel in the ABA triblock copolymer at low temperatures. In these SWCNT/copolymer materials the storage and loss moduli have been observed to increase with time at fixed temperature. When triblock copolymer gels are used as the matrix, we find that the aging effect is erased by cycling the temperature through the gel transition. An increase in storage modulus is observed upon cooling before the gel formation. However, the moduli revert back to lower values when the gel dissolves on heating. We believe this is a result of semi-permanent nanotube junctions being pulled apart when the gel forms. This reversibility is not observed when the nanotubes are dispersed in solutions of diblock copolymer, which do not form gels.

  8. Catalytic Hydrogenolysis of 5-Carbon Sugar Alcohols

    SciTech Connect

    Zacher, Alan H.; Frye, John G.; Werpy, Todd A.; Miller, Dennis J.

    2005-01-01

    PNNL, in cooperation with the USDOE and CRADA partners, National Corn Growers Association and Archer Daniels Midland, has developed a new class of catalysts based on Nickel and Rhenium with very effective performance for highly selective, high conversion hydrogenolysis of five–carbon sugar alcohols to useful glycols. The Ni-Re catalyst appears to exhibit preferential hydrogenolysis of the carbon-carbon bonds of secondary carbons over primary carbons of the 5-carbon sugar alcohols tested. In addition, the catalyst has demonstrated significant and unique primary C-O bond hydrogenolysis activity in its ability to convert glycerol into 1,2- propylene glycol, which is then stable in the presence of this class of catalysts. The rhenium containing catalysts are found to have higher activity and better selectivity to desired glycols than previously reported catalysts. A continuous flow reactor lifetime test of over 1500 hours also demonstrated the requisite high stability for an industrially attractive process.

  9. Alcohol-induced drying of carbon nanotubes and its implications for alcohol/water separation: A molecular dynamics study

    NASA Astrophysics Data System (ADS)

    Tian, Xingling; Yang, Zaixing; Zhou, Bo; Xiu, Peng; Tu, Yusong

    2013-05-01

    Alcohols are important products in chemical industry, but separating them from their aqueous solutions is very difficult due to the hydrophilic nature of alcohols. Based on molecular dynamics simulations, we observe a striking nanoscale drying phenomenon and suggest an energy-saving and efficient approach toward alcohol/water separation by using single-walled carbon nanotubes (SWNTs). We use various common linear alcohols including C1-C6 1-alcohols and glycerol for demonstration (the phenol is also used as comparison). Our simulations show that when SWNTs are immersed in aqueous alcohols solutions, although the alcohols concentration is low (1 M), all kinds of alcohols can induce dehydration (drying) of nanotubes and accumulate inside wide [(13, 13)] and narrow [(6, 6) or (7, 7)] SWNTs. In particular, most kinds of alcohols inside the narrow SWNTs form nearly uniform 1D molecular wires. Detailed energetic analyses reveal that the preferential adsorption of alcohols over water inside nanotubes is attributed to the stronger dispersion interactions of alcohols with SWNTs than water. Interestingly, we find that for the wide SWNT, the selectivity for 1-alcohols increases with the number of alcohol's carbon atoms (Ncarbon) and exhibits an exponential law with respect to Ncarbon for C1-C5 1-alcohols; for narrow SWNTs, the selectivity for 1-alcohols is very high for methanol, ethanol, and propanol, and reaches a maximum when Ncarbon = 3. The underlying physical mechanisms and the implications of these observations for alcohol/water separation are discussed. Our findings provide the possibility for efficient dehydration of aqueous alcohols (and other hydrophilic organic molecules) by using SWNT bundles/membranes.

  10. Separation and concentration of lower alcohols from dilute aqueous solutions

    DOEpatents

    Moore, Raymond H.; Eakin, David E.; Baker, Eddie G.; Hallen, Richard T.

    1991-01-01

    A process for producing, from a dilute aqueous solution of a lower (C.sub.1 -C.sub.5) alcohol, a concentrated liquid solution of the alcohol in an aromatic organic solvent is disclosed. Most of the water is removed from the dilute aqueous solution of alcohol by chilling sufficiently to form ice crystals. Simultaneously, the remaining liquid is extracted at substantially the same low temperature with a liquid organic solvent that is substantially immiscible in aqueous liquids and has an affinity for the alcohol at that temperature, causing the alcohol to transfer to the organic phase. After separating the organic liquid from the ice crystals, the organic liquid can be distilled to enrich the concentration of alcohol therein. Ethanol so separated from water and concentrated in an organic solvent such as toluene is useful as an anti-knock additive for gasoline.

  11. Hand antiseptics: rubs versus scrubs, alcoholic solutions versus alcoholic gels.

    PubMed

    Pietsch, H

    2001-08-01

    This report describes three different investigations undertaken to demonstrate the advantage of fluid alcoholic hand disinfectants. In the first study, the skin compatibility of Sterillium, a liquid alcoholic rub-in hand disinfectant was compared with that of Hibiscrub, a water-based handwashing antiseptic. Using various parameters such as image analysis of removed squames (D-squames), skin roughness or transepidermal water loss, Hibiscrub was found to be significantly inferior to Sterillium. Hibiscrub caused skin irritation in 15 volunteers who could not complete the test. In a second study, the microbicidal efficacy of Sterillium and Hibiscrub was tested in surgical hand disinfection. The microbial reduction by Sterillium was significantly greater than that of Hibiscrub, immediately after application as well as after the surgical procedure. In a third study, certain alcoholic gels were tested according to the EN 1500 'hygienic hand disinfection'. None of the gels tested passed the EN 1500 within 30s. However, Sterillium met the EN 1500 requirement within 30s. We conclude that Sterillium is superior to Hibiscrub in terms of skin tolerance and microbicidal efficacy in surgical hand disinfection. It is also superior to alcoholic gels. PMID:11759022

  12. 27 CFR 19.385 - Making alcohol or water solutions of denaturants.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2012-04-01 2012-04-01 false Making alcohol or water solutions of denaturants. 19.385 Section 19.385 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO... alcohol or water solutions of denaturants. If a proprietor uses a denaturant that is difficult to...

  13. 27 CFR 19.385 - Making alcohol or water solutions of denaturants.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2011-04-01 2011-04-01 false Making alcohol or water solutions of denaturants. 19.385 Section 19.385 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO... alcohol or water solutions of denaturants. If a proprietor uses a denaturant that is difficult to...

  14. Measurement of Temperature Dependence of Surface Tension of Alcohol Aqueous Solutions by Maximum Bubble Pressure Method

    NASA Astrophysics Data System (ADS)

    Ono, Naoki; Kaneko, Takahiro; Nishiguchi, Shotaro; Shoji, Masahiro

    The surface tension of some high-carbon alcohol aqueous solutions increases as the temperature rises above a certain temperature. There have been attempts to use such special solutions in thermal devices to promote heat transfer. In this study, the authors analyzed the temperature dependence of surface tension of these solutions to investigate this peculiar characteristic in detail. The test fluids were butanol and pentanol aqueous solutions as peculiar solutions, while pure water and ethanol aqueous solution were normal fluids. First, the authors adopted Wilhelmy's method to measure the surface tension during heating, but found that the influence of evaporation of the solution could not be completely eliminated. In this study, the maximum bubble pressure method was employed, which made it possible to isolate the measured solution from ambient air and eliminate the influence of evaporation of the solution. The authors succeeded in measuring the temperature dependence of surface tension, and obtained more reasonable data.

  15. Surface Tension Characteristics of Aqueous Lithium Bromide Solution with Alcoholic Surfactant

    NASA Astrophysics Data System (ADS)

    Sasaki, Naoe; Ogawa, Kiyoshi

    At present, the combination of aqueous lithium bromide (LiBr) solution as an absorbent and water as a refrigerant have widely been used as the working fluid for absorption refrigerating machines. In order to obtain absorption enhancement of water vapor into the LiBr solution by Marangoni convection, an alcoholic surfactant is being added in the LiBr solution. In that case, the surface tension of the LiBr solution with the surfactant plays an important role for the vapor absorption. In this study, the surface tensions of the LiBr solution with several alcoholic surfactants such as 1-butanol, 1-hexanol, 2-ethyl-1-butanol, 2-methyl-1-pentanol, 1-heptanol, 1-octanol and 2-ethyl-1-hexanol were measured by Wilhelmy plate method. As a result, the surface tensions of 50 wt% LiBr solution with several surfactants were obtained over the LiBr solution temperature range from 298 K to 318 K and the surfactant concentration range from 0 to 104 ppm by mass. The measured surface tension has decreased with the increasing number of carbons included in the surfactant at constant concentration, and the surface tension has increased with the increasing temperature of 50 wt% LiBr solution. The surface tension increase of 1-octanol became greater than any other surfactant used in this work. The effective carbon number of the surfactant for the absorption enhancement was in the range from 7 to 8.

  16. 27 CFR 19.385 - Making alcohol or water solutions of denaturants.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2014-04-01 2014-04-01 false Making alcohol or water solutions of denaturants. 19.385 Section 19.385 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE BUREAU, DEPARTMENT OF THE TREASURY ALCOHOL DISTILLED SPIRITS PLANTS...

  17. Aquifer washing by micellar solutions: 2. DNAPL recovery mechanisms for an optimized alcohol surfactant solvent solution

    NASA Astrophysics Data System (ADS)

    Martel, Richard; Lefebvre, René; Gélinas, Pierre J.

    1998-03-01

    A large sand column experiment is used to illustrate the principles of complex organic contaminants (DNAPL) recovery by a chemical solution containing an alcohol ( n-butanol), a surfactant (Hostapur SAS), and two solvents ( d-limonene and toluene). The washing solution is pushed by viscous polymer solutions to keep the displacement stable. The main NAPL recovery mechanisms identified are: (1) immiscible displacement by oil saturation increase (oil swelling), oil viscosity reduction, interfacial tension lowering, and relative permeability increase; (2) miscible NAPL displacement by solubilization. Most of the NAPL was recovered in a Winsor, type II system ahead of the washing solution. The 0.8 pore volume (PV) of alcohol-surfactant-solvent solution injected recovered more than 89% of the initial residual DNAPL saturation (0.195). Winsor system types were determined by visual observation of phases and confirmed by electrical resistivity measurements of phases and water content measurements in the oleic phase. Viscosity and density lowering of the oleic phase was made using solvents and alcohol transfer from the washing solution. Small sand column tests are performed to check different rinsing strategies used to minimize washing solution residual ingredients which can be trapped in sediments. An alcohol/surfactant rinsing solution without solvent, injected behind the washing solution, minimizes solvent trapping in sediments. More than five pore volumes of polymer solution and water must be injected after the rinsing solution to decrease alcohol and SAS concentrations in sediments to an acceptable level. To obtain reasonable trapped surfactant concentrations in sediments, the displacement front between the rinsing solution and the subsequent the following polymer solution has to be stable.

  18. Oxidative alkoxylation of phosphine in alcohol solutions of copper halides

    NASA Astrophysics Data System (ADS)

    Polimbetova, G. S.; Borangazieva, A. K.; Ibraimova, Zh. U.; Bugubaeva, G. O.; Keynbay, S.

    2016-08-01

    The phosphine oxidation reaction with oxygen in alcohol solutions of copper (I, II) halides is studied. Kinetic parameters, intermediates, and by-products are studied by means of NMR 31Р-, IR-, UV-, and ESR- spectroscopy; and by magnetic susceptibility, redox potentiometry, gas chromatography, and elemental analysis. A reaction mechanism is proposed, and the optimum conditions are found for the reaction of oxidative alkoxylation phosphine.

  19. Degradation of halogenated carbons in alkaline alcohol

    NASA Astrophysics Data System (ADS)

    Nakagawa, Seiko; Shimokawa, Toshinari

    2002-02-01

    1,1,2-Trichloro-trifluoroethane, 1,2-dibromo-tetrafluoroethane, 2,3,4,6-tetrachlorophenol, 1,2,4-trichlorobenzene, and 2,4,6-trichloroanisole were dissolved in alkaline isopropyl alcohol and irradiated with 60Co gamma rays after purged with pure nitrogen gas. The concentration of the hydroxide ions and the parent molecules decreased with the dose, while that of the halide ions and the organic products, with less halogen atoms than the parent, increased. Chain degradation will occur in alkaline isopropyl alcohol.

  20. Does Disease Matter? Incorporating Solution-Focused Brief Therapy in Alcoholism Treatment.

    ERIC Educational Resources Information Center

    Osborn, Cynthia J.

    1997-01-01

    Surveyed alcoholism counselors (N=284) to determine whether the disease concept of alcoholism precludes acceptance and use of Solution-Focused Brief Therapy (SFBT) in alcoholism treatment. Results suggest that SFBT may be feasible for alcoholism treatment and that endorsement of the disease concept is compatible with the principles of SFBT. (EMK)

  1. Aquifer washing by micellar solutions: 1. Optimization of alcohol-surfactant-solvent solutions

    NASA Astrophysics Data System (ADS)

    Martel, Richard; Gélinas, Pierre J.; Desnoyers, Jacques E.

    1998-03-01

    Phase diagrams were used for the formulation of alcohol-surfactant-solvent and to identify the DNAPL (Dense Non Aqueous Phase Liquid) extraction zones. Four potential extraction zones of Mercier DNAPL, a mixture of heavy aliphatics, aromatics and chlorinated hydrocarbons, were identified but only one microemulsion zone showed satisfactory DNAPL recovery in sand columns. More than 90 sand column experiments were performed and demonstrate that: (1) neither surfactant in water, alcohol-surfactant solutions, nor pure solvent can effectively recover Mercier DNAPL and that only alcohol-surfactant-solvent solutions are efficient; (2) adding salts to alcohol-surfactant or to alcohol-surfactant-solvent solutions does not have a beneficial effect on DNAPL recovery; (3) washing solution formulations are site specific and must be modified if the surface properties of the solids (mineralogy) change locally, or if the interfacial behavior of liquids (type of oil) changes; (4) high solvent concentrations in washing solutions increase DNAPL extraction but also increase their cost and decrease their density dramatically; (5) maximum DNAPL recovery is observed with alcohol-surfactant-solvent formulations which correspond to the maximum solubilization in Zone C of the phase diagram; (6) replacing part of surfactant SAS by the alcohol n-butanol increases washing solution efficiency and decreases the density and the cost of solutions; (7) replacing part of n-butanol by the nonionic surfactant HOES decreases DNAPL recovery and increases the cost of solutions; (8) toluene is a better solvent than D-limonene because it increases DNAPL recovery and decreases the cost of solutions; (9) optimal alcohol-surfactant-solvent solutions contain a mixture of solvents in a mass ratio of toluene to D-limonene of one or two. Injection of 1.5 pore volumes of the optimal washing solution of n-butanol-SAS-toluene- D-limonene in water can recover up to 95% of Mercier DNAPL in sand columns. In the first

  2. [Toxicological-hygienic assessment of the low-alcohol tonic (energizing) carbonated drinks].

    PubMed

    Istomin, A V; Rumiantseva, L A; Mikhaĭlov, I G; Novichkova, N I; Ponomarenko, I I; Kutakova, N S

    2013-01-01

    The impact of the low-alcohol tonic (energizing) carbonated drinks on biochemical and hematological indices, on the functional state of the central nervous system and cardiovascular system was studied within the experiment over the outbred white male rats. The gained results were compared to indices of animals receiving the same concentrated solution of ethanol used for drinks preparation as well as to figures of intact group animals. The results gained from all compared animals groups had no significant differences. PMID:24000701

  3. Silver Nanoparticle Fabrication by Laser Ablation in Polyvinyl Alcohol Solutions

    NASA Astrophysics Data System (ADS)

    Halimah Mohamed., K.; Mahmoud Goodarz, Naseri; Amir, Reza Sadrolhosseini; Arash, Dehzangi; Ahmad, Kamalianfar; Elias, B. Saion; Reza, Zamiri; Hossein Abastabar, Ahangar; Burhanuddin, Y. Majlis

    2014-07-01

    A laser ablation technique is applied for synthesis of silver nanoparticles in different concentrations of polyvinyl alcohol (PVA) aqueous solution. The ablation of high pure silver plate in the solution is carried out by a nanosecond Q-switched Nd:YAG pulsed laser. X-ray diffraction and transmission electron microscopy are implemented to explore the particles sizes. The effects of PVA concentrations on the absorbance of the silver nanoparticles are studied as well, by using a UV-vis spectrophotometer. The preparation process is carried out for deionized water as a reference sample. The comparison of the obtained results with the reference sample shows that the formation efficiency of nanoparticles in PVA is much higher and the sizes of particles are also smaller.

  4. Interaction of Ethyl Alcohol Vapor with Sulfuric Acid Solutions

    NASA Technical Reports Server (NTRS)

    Leu, Ming-Taun

    2006-01-01

    We investigated the uptake of ethyl alcohol (ethanol) vapor by sulfuric acid solutions over the range approx.40 to approx.80 wt % H2SO4 and temperatures of 193-273 K. Laboratory studies used a fast flow-tube reactor coupled to an electron-impact ionization mass spectrometer for detection of ethanol and reaction products. The uptake coefficients ((gamma)) were measured and found to vary from 0.019 to 0.072, depending upon the acid composition and temperature. At concentrations greater than approx.70 wt % and in dilute solutions colder than 220 K, the values approached approx.0.07. We also determined the effective solubility constant of ethanol in approx.40 wt % H2SO4 in the temperature range 203-223 K. The potential implications to the budget of ethanol in the global troposphere are briefly discussed.

  5. Silver(I)-Catalyzed Three-Component Reaction of Propargylic Alcohols, Carbon Dioxide and Monohydric Alcohols: Thermodynamically Feasible Access to β-Oxopropyl Carbonates.

    PubMed

    Zhou, Zhi-Hua; Song, Qing-Wen; Xie, Jia-Ning; Ma, Ran; He, Liang-Nian

    2016-07-20

    A silver(I)-catalyzed three-component reaction of propargylic alcohols, CO2 , and monohydric alcohols was successfully developed for the synthesis of β-oxopropyl carbonates. As such, a series of β-oxopropyl carbonates were exclusively produced in excellent yields (up to 98 %), even under atmospheric pressure of CO2 . The silver catalyst works efficiently for both the carboxylative cyclization of propargylic alcohols with CO2 and subsequent transesterification of α-alkylidene cyclic carbonates with monohydric alcohols; thus this tandem process performs smoothly under mild conditions. This work provides a versatile and thermodynamically favorable approach to dissymmetric dialkyl carbonates. PMID:27237704

  6. 27 CFR 19.385 - Making alcohol or water solutions of denaturants.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2013-04-01 2013-04-01 false Making alcohol or water... alcohol or water solutions of denaturants. If a proprietor uses a denaturant that is difficult to dissolve... water prior to its use in the production of denatured spirits. However, the proof of the...

  7. Evolution of electrical discharge channel in isopropyl alcohol solution

    NASA Astrophysics Data System (ADS)

    Panov, V. A.; Vasilyak, L. M.; Pecherkin, V. Ya; Vetchinin, S. P.; Kulikov, Yu M.; Son, E. E.

    2015-11-01

    Evolution of the spark channel created by the high voltage pulse generator in 15% isopropyl alcohol solution in tap water was investigated experimentally. Fast camera images show the start of spark discharge channel with the anode region glowing, which is due to ionization-overheating instability near the surface of anode electrode. Measured propagation velocity is about 4 m/s and points to thermal process of channel evolution. Partial discharges in gas bubbles near the spark channel were observed. When the channel bridges the gap the cathode flash of lightning occurs which is much brighter than anode glowing and channel one. After destruction of the spark channel the cathode glowing stays for a longer period than anode one.

  8. Carbon nanofibers synthesized by decomposition of alcohol at atmospheric pressure

    NASA Astrophysics Data System (ADS)

    Jiang, N.; Koie, R.; Inaoka, T.; Shintani, Y.; Nishimura, K.; Hiraki, A.

    2002-07-01

    In the present study, we fabricated the carbon nanofibers (CNFs) by decomposition of methyl alcohol at atmospheric pressure. The CNFs were grown on Ni/Si substrates using simplified hot-filament chemical vapor deposition equipment. The deposits mainly consist of the semicrystalline CNFs, in which a few of carbon nanotubes are included. On the 30-nm-thick Ni/Si substrates, the mean length of the CNFs is 2-3 mum, and their average diameter is less than 100 nm. The as-deposited CNFs were evaluated by both scanning and transmission electron microscopes. The field-electron-emission properties of CNFs were characterized as well.

  9. CATALYZED OXIDATION OF URANIUM IN CARBONATE SOLUTIONS

    DOEpatents

    Clifford, W.E.

    1962-05-29

    A process is given wherein carbonate solutions are employed to leach uranium from ores and the like containing lower valent uranium species by utilizing catalytic amounts of copper in the presence of ammonia therein and simultaneously supplying an oxidizing agent thereto. The catalysis accelerates rate of dissolution and increases recovery of uranium from the ore. (AEC)

  10. [Photodegradation of paracetamol in carbonate solution].

    PubMed

    Gao, Ying; Yang, Xi; Liu, Yu

    2008-03-01

    The photodegradation of paracetamol in the solution of carbonate with comparably environmental concentration was studied through kinetics method. Experiments were carried out to compare the different photodegradation effects of paracetamol in the solution of carbonate radical and hydroxyl radical. The effects of such factors, pH, nitrate, humic matters, chloride sodium, calcium and magnesium were also analyzed. The products of the photodegradation were identified with GC/MS, and the degradation mechanism of paracetamol was discussed. The results indicate that, the scondary reaction rate constant (k(a)) between paracetamol and carbonate radical is 5.0 x 10(7) L (mol s)(-1), which is lower than that with hydroxyl radical [k(b) = 8.1 x 10(9) L (mol s)(-1)]. But in natural aqueous system, the stable concentration of carbonate radical is much higher than that of hydroxyl. Therefore, the effect of carbonate radical on paracetamol approximately equals to that of hydroxyl radical. The degradation rate of paracetamol increases when the system was changed with higher pH, adding of nitrate, chloride sodium, calcium and magnesium which increase the rigidity of the water, while decreases when the SRFA is present. PMID:18649521

  11. Recovery of anhydrous Na{sub 2}SO{sub 4} from SO{sub 2}-scrubbing liquor by extractive crystallization: Liquid-liquid equilibria for aqueous solutions of sodium carbonate, sulfate, and/or sulfite plus acetone, 2-propanol, or tert-butyl alcohol

    SciTech Connect

    Lynn, S.; Cos, R.; Prausnitz, J.M.; Schiozer, A.L.; Jaecksch, W.L.

    1996-11-01

    Sodium carbonate is a superior scrubbing agent for removing SO{sub 2} from combustion gases, but the resulting sodium sulfate (or sulfite) must be recovered for environmental reasons. Recovery by evaporative crystallization is energy-intensive; extractive crystallization provides an attractive alterative when technically feasible. Liquid/liquid equilibrium data were determined for two-phase mixtures containing aqueous solutions of sodium carbonate, sulfate, or sulfite and a polar organic solvent: acetone, 2-propanol, and 2-methylpropan-1-ol (i.e., tert-butyl alcohol). In the salt-saturated two-phase region, data were obtained between the lower consolute temperature and 60 C (50 C for acetone). data were also obtained at 35 C for liquid/liquid systems that were subsaturated with their respective salts and for liquid/liquid systems with overall molar ratios of sodium sulfite/sodium sulfate fixed at 25/75, 50/50, and 75/25. In the latter systems, it was found that the sulfite/sulfate ratios in the organic and aqueous phases were the same, i.e., there is no selectivity by these solvents for one salt relative to the other. The data show that any one of these solvents can be used to extract water from a concentrated solution of either sodium sulfite or sodium sulfate in a countercurrent extractor at 35 C, causing the anhydrous salt to crystallize. The wet solvent can be dried for recycle in a similar countercurrent operation at 35 C, using a saturated solution of Na{sub 2}CO{sub 3} as the drying agent. The number of moles of carbonate required for drying does not exceed the number of moles of sulfite-plus-sulfate precipitated. The process energy is about 0% of that required for single-stage evaporative crystallization of the same liquor.

  12. Olfactory Impact of Higher Alcohols on Red Wine Fruity Ester Aroma Expression in Model Solution.

    PubMed

    Cameleyre, Margaux; Lytra, Georgia; Tempere, Sophie; Barbe, Jean-Christophe

    2015-11-11

    This study focused on the impact of five higher alcohols on the perception of fruity aroma in red wines. Various aromatic reconstitutions were prepared, consisting of 13 ethyl esters and acetates and 5 higher alcohols, all at the average concentrations found in red wine. These aromatic reconstitutions were prepared in several matrices. Sensory analysis revealed the interesting behavior of certain compounds among the five higher alcohols following their individual addition or omission. The "olfactory threshold" of the fruity pool was evaluated in several matrices: dilute alcohol solution, dilute alcohol solution containing 3-methylbutan-1-ol or butan-1-ol individually, and dilute alcohol solution containing the mixture of five higher alcohols, blended together at various concentrations. The presence of 3-methylbutan-1-ol or butan-1-ol alone led to a significant decrease in the "olfactory threshold" of the fruity reconstitution, whereas the mixture of alcohols raised the olfactory threshold. Sensory profiles highlighted changes in the perception of fruity nuances in the presence of the mixture of higher alcohols, with specific perceptive interactions, including a relevant masking effect on fresh- and jammy-fruit notes of the fruity mixture in both dilute alcohol solution and dearomatized red wine matrices. When either 3-methylbutan-1-ol or butan-1-ol was added to the fruity reconstitution in dilute alcohol solution, an enhancement of butyric notes was reported with 3-methylbutan-1-ol and fresh- and jammy-fruit with butan-1-ol. This study, the first to focus on the impact of higher alcohols on fruity aromatic expression, revealed that these compounds participate, both quantitatively and qualitatively, in masking fruity aroma perception in a model fruity wine mixture. PMID:26529563

  13. Thermodynamics of hydrogen bonding of weak bases in alcohol solutions: Calorimetry of solution, IR-spectroscopy and vapor pressure analysis

    NASA Astrophysics Data System (ADS)

    Zaitseva, Ksenia V.; Varfolomeev, Mikhail A.; Solomonov, Boris N.

    2012-06-01

    The properties of solutes and their reactivity in aliphatic alcohols significantly depend on the formation of hydrogen bonds. In this work, calorimetric, FTIR-spectroscopic and gas chromatographic vapor pressure studies of hydrogen bonds of weak bases in solution of aliphatic alcohols were carried out. Enthalpies of solutions at infinite dilution of ketones, nitriles and acetates in methanol and octan-1-ol were measured. Obtained from the calorimetric data, the enthalpies of specific interaction of weak bases in aliphatic alcohols unexpectedly found to be positive. IR spectra of solutions of ketones in aliphatic alcohols at infinite dilution were measured at different temperatures. Enthalpies of specific interaction in studied systems obtained from the spectroscopic data confirmed the endothermic process and are in good agreement with calorimetric results. Gibbs energies and entropies of specific interaction of weak bases in aliphatic alcohols were determined. Obtained results show, that the hydrogen bonding process of weak bases in aliphatic alcohols differs substantially from the formation of complexes 1:1 ROH⋯B (B - weak proton acceptor) in aprotic media. The complicated process of hydrogen bonding of weak bases in aliphatic alcohols apparently is controlled by the entropy factor, because these values are above zero.

  14. Aqueous solution dispersement of carbon nanotubes

    NASA Technical Reports Server (NTRS)

    Kim, Jae-Woo (Inventor); Park, Cheol (Inventor); Choi, Sang H. (Inventor); Lillehei, Peter T. (Inventor); Harrison, Joycelyn S. (Inventor)

    2011-01-01

    Carbon nanotubes (CNTs) are dispersed in an aqueous buffer solution consisting of at least 50 weight percent water and a remainder weight percent that includes a buffer material. The buffer material has a molecular structure defined by a first end, a second end, and a middle disposed between the first and second ends. The first end is a cyclic ring with nitrogen and oxygen heteroatomes, the middle is a hydrophobic alkyl chain, and the second end is a charged group.

  15. Electrocatalytic oxidation of alcohols by a carbon-supported Rh porphyrin.

    PubMed

    Yamazaki, Shin-ichi; Yao, Masaru; Fujiwara, Naoko; Siroma, Zyun; Yasuda, Kazuaki; Ioroi, Tsutomu

    2012-05-01

    A Rh porphyrin on carbon black was shown to catalyze the electro-oxidation of several aliphatic alcohols (ethanol, 1-propanol, and 2-propanol) and benzyl alcohols. The overpotentials for alcohol oxidation were very low. The reaction mechanism and substrate specificity are discussed. PMID:22450541

  16. Carbon-coated magnetic palladium: applications in partial oxidation of alcohols and coupling reactions.

    EPA Science Inventory

    Magnetic carbon supported Pd catalyst has been synthesized via in situ generation of nanoferrites and incorporation of carbon from renewable cellulose via calcination; catalyst can be used for oxidation of alcohols, amination reaction and arylation of aryl halides (cross coupli...

  17. Alcohol/"low-dose" carbon tetrachloride-induced cirrhosis in rats using different methods of alcohol feeding.

    PubMed

    Plummer, J L; Hall, P D; Cmielewski, P L; Iisley, A H; Ahem, M J

    1994-12-01

    Cirrhosis may be reliably produced in rats by exposing them to low levels of carbon tetrachloride vapor while feeding alcohol in the Lieber-DeCarli liquid diet. This study aimed to determine whether alternative cheaper and more convenient ways of feeding alcohol would also allow the production of cirrhosis. Animals were fed alcohol in the Lieber-DeCarli diet, in a gel diet, or by addition of alcohol + sucrose to their drinking water, and were exposed to carbon tetrachloride vapor 6 hr/night, 5 nights/week. After 12 weeks of treatment, all animals (4 of 4) receiving alcohol in the Lieber-DeCarli diet, but only two in each of the gel and drinking water groups, were cirrhotic. The variable results with the gel diet may be due to loss of alcohol by evaporation from the gel. Alcohol intake in the group receiving alcohol in drinking water was greater than in those receiving Lieber-DeCarli diet. We suggest that the increased carbohydrate intake due to addition to sucrose to the water exerted a protective effect on the liver. PMID:7695051

  18. Alcohol

    MedlinePlus

    ... How Can I Help a Friend Who Cuts? Alcohol KidsHealth > For Teens > Alcohol Print A A A ... you can make an educated choice. What Is Alcohol? Alcohol is created when grains, fruits, or vegetables ...

  19. Femtosecond Laser Ablation of Frozen Alcohols for Deposition of Diamond-Like Carbon Thin Films

    NASA Astrophysics Data System (ADS)

    Okoshi, Masayuki; Inoue, Wataru; Inoue, Narumi

    2008-06-01

    A 790 nm, 130 fs Ti:sapphire laser pulse ablated various frozen alcohols (CnH2n + 1OH, n = 1-6) to deposit diamond-like carbon (DLC) thin films. The larger the carbon number (n) of the alcohols, the higher the hydrogen content of the DLC films; the sp3 carbon content ranged from 35 to 45%. The hydrogen content caused a change in the optical band gap of the films. Moreover, the deposition rate of the films increased linearly as the carbon number increased. The deposition rate did not simply relate to the amount of carbon species ejected from the frozen alcohols. Even though carbon species were largely generated, the ejected oxygen radicals etched the carbon to lower the deposition rate. When we used frozen benzene as a laser target, DLC thin films were not deposited. By dissolving boric acid in an alcohol, we could deposit boron-doped DLC thin films.

  20. Adsorption of Methylene Blue from Aqueous Solutions by Polyvinyl Alcohol/Graphene Oxide Composites.

    PubMed

    Yang, Xiaoxia; Li, Yanhui; Du, Qiuju; Wang, Xiaohui; Hu, Song; Chen, Long; Wang, Zonghua; Xia, Yanzhi; Xia, Linhua

    2016-02-01

    As a new member of the carbon family, graphene oxide (GO) has shown excellent adsorption ability to micro-pollutants in aqueous solutions. However, its tiny size makes it difficult to be removed from aqueous solutions using the conventional separation methods, which limits its practical application in the environmental protection. In this study, polyvinyl alcohol (PVA) was used as carrier immobilizing GO, and novel PVA/GO composites were prepared. The morphology and physicochemical properties of the composites were characterized by SEM, FTIR and TGA analysis. The adsorption properties of methylene blue (MB) onto the composites were studied through investigating the experimental parameters such as solution pH, adsorbent dosage, contact time and temperature. The isotherm data were analyzed using the Langmuir, Freundlich and Dubinin-Radushkevich models. The calculated maximum adsorption capacity reached 476.2 mg/g at 50% GO content. The pseudo-first-order kinetic, pseudo-second-order kinetic and intra-particle diffusion models were used to explore the adsorption kinetics. The results showed that the dynamic data were fitted to the pseudo-second-order kinetic model. PMID:27433669

  1. Mechanical and dielectric properties of carbon nanotubes/poly (vinyl alcohol) nanocomposites

    NASA Astrophysics Data System (ADS)

    Amrin, Sayed; Deshpande, V. D.

    2016-05-01

    In this work, two series of nanocomposites of poly(vinyl alcohol) (PVA) incorporated with multiwalled carbon nanotubes (MWNT) and carboxyl functionalized multiwalled carbon nanotubes (MWNT-COOH) were fabricated using solution-cast method and their tensile and dielectric properties were studied. Tensile tests were carried out on composite films of MWNT/PVA and MWNT-COOH/PVA for different loading levels. Results show that overall mechanical properties of the MWNT-COOH/PVA composite was greatly improved as compared to the MWNT/PVA film. The dielectric properties of nanocomposites were investigated in a frequency range from 0.1Hz to 10MHz at room temperature respectively. Compared to MWNT/PVA composites, higher dielectric constant and ac conductivity was achieved in MWNT-COOH/PVA nanocomposite, which can be well explained by the interfacial polarization effect.

  2. Nucleation of CaCO3 polymorphs from a colloidal alcoholic solution of Ca(OH)2 nanocrystals exposed to low humidity conditions

    NASA Astrophysics Data System (ADS)

    Gomez-Villalba, L. S.; López-Arce, P.; Fort, R.

    2012-01-01

    A study of the stability of calcium carbonate polymorphs formed as a result of the carbonation process from an alcoholic colloidal solution of nanocrystals of Ca(OH)2 in low relative humidity (RH) conditions (33% and 54% RH) is presented in this research. The crystalline behavior, the time dependence of nucleation and the phases' transformations as a result of exposure to low humidity conditions are evaluated. The carbonation process is slow, starting with the nucleation of amorphous calcium carbonate, associated to an amorphization process that affects both the portlandite (Ca(OH)2) and the initial unstable CaCO3 polymorphs. The excess of alcohol in the solution decreases the surface tension and the nucleation is accelerated by the fast evaporation of the solvent, which avoids the particles to diffuse to their lowest energy sites, giving smaller particles with lower crystallinity as RH decreases.

  3. Solubility of the sesquiterpene alcohol patchoulol in supercritical carbon dioxide

    PubMed Central

    Hybertson, Brooks M.

    2009-01-01

    The solubility of the sesquiterpene alcohol patchoulol in supercritical carbon dioxide was measured at P ranging from 10.0 MPa to 25.0 MPa and T of 40.0 and 50.0 °C using a simple microsampling type apparatus with a 100.5 µL sample loop to remove aliquots for off-line analysis. The system was first validated using vanillin with off-line spectrophotometric analysis, then utilized for patchoulol measurements with off-line GC-MS analysis. The measured solubility of patchoulol in supercritical CO2 ranged from mole fractions of 0.43 × 10−3 at 10.0 MPa and 50.0 °C to 9.45 × 10−3 at 25.0 MPa and 40.0 °C. PMID:19424449

  4. A Raman Study of Alcoholic Lithium Perchlorate Solutions in the Glassy State

    NASA Astrophysics Data System (ADS)

    Kanno, H.; Honshoh, M.; Yamauchi, S.

    1995-03-01

    Raman spectra of alcoholic lithium Perchlorate solutions (alcohol = methanol and ethanol) were measured as a function of LiClO4 concentration. The Raman band due to nearly free hydrogen bonds shows peculiar concentration dependences: (1) its frequency shifts with LiClO4 concentration in contrast to alcoholic LiX solutions (X = CI and Br), in which the Raman band due to solvated halide ions shows little frequency change with LiX concentration, and (2) the half band width shows anomalous changes with LiX concentration. Non-ionized LiClO4 species in alcohol coupled with the changes of solution structure are the major cause for this peculiar behavior.

  5. Alcohol

    MedlinePlus

    ... Text Size: A A A Listen En Español Alcohol Wondering if alcohol is off limits with diabetes? Most people with diabetes can have a moderate amount of alcohol. Research has shown that there can be some ...

  6. Alcohol

    MedlinePlus

    If you are like many Americans, you drink alcohol at least occasionally. For many people, moderate drinking ... risky. Heavy drinking can lead to alcoholism and alcohol abuse, as well as injuries, liver disease, heart ...

  7. Molecular Arrangement and Surface Tension of Alcohol Solutions.

    PubMed

    Phan, Chi M; Nguyen, Cuong V; Pham, Thuy T T

    2016-04-28

    This study investigated the relationship between molecular arrangement and surface tension of water mixtures with methanol and ethanol. It has been found that the molecular structure of interfacial zone was deterministically correlated to alcohol concentration. From the water dipole moment, an interfacial boundary was defined. The boundary then was used to calculate the water and alcohols in the interfacial zone, which was then used to calculate the surface tension. The prediction from simulated data closely followed the experimental data. The analysis revives the relevance of the molecular arrangement, which had been the main focus in the early 20th century, in quantification of surface energy. The results can supplement the current thermodynamic analysis to correctly predict the surface adsorption. PMID:27054524

  8. Theoretical Investigation on Alcohol Sensing of Glycine-Coated Carbon Nanotubes

    NASA Astrophysics Data System (ADS)

    Jiang, Tao; Kussow, Gary; Kwon, Young-Kyun

    2007-03-01

    It has been observed that single walled carbon nanotube field effect transistors (SWNT-FET) coated with glycine can be used as alcohol sensors. The original semiconducting glycine-coated SWNT-FET have been changed to be metalic in the presence of alcohol. Using ab initio density functional theory, we compute the structural and electronic properties of carbon nanotubes coated with glycine in the absence or in the presence of alcohol (Isopropanol) to investigate alcohol sensing mechanism. To demonstrate specificity of such glycine-coated SWNT-FETs on alcohol, we also study those properties in the presence of other molecules, such as acetone and water. Furthermore, we investigate the effect of an external fields on glycine-coated SWNT with IPA, and indentify the gate-electric-field screening in SWNT-FET to be a major role for alcohol sensing.

  9. Alcohol

    MedlinePlus

    ... Got Homework? Here's Help White House Lunch Recipes Alcohol KidsHealth > For Kids > Alcohol Print A A A Text Size What's in ... What Is Alcoholism? Say No en español El alcohol Getting the Right Message "Hey, who wants a ...

  10. Enthalpic parameters of interaction between diglycylglycine and polyatomic alcohols in aqueous solutions

    NASA Astrophysics Data System (ADS)

    Mezhevoi, I. N.; Badelin, V. G.

    2015-12-01

    Integral enthalpies of solution Δsol H m of diglycylglycine in aqueous solutions of glycerol, ethylene glycol, and 1,2-propylene glycol are measured via solution calorimetry. The experimental data are used to calculate the standard enthalpies of solution (Δsol H°) and transfer (Δtr H°) of the tripeptide from water to aqueous solutions of polyatomic alcohols. The enthalpic pairwise coefficients h xy of interactions between the tripeptide and polyatomic alcohol molecules are calculated using the McMillan-Mayer solution theory and are found to have positive values. The findings are discussed using the theory of estimating various types of interactions in ternary systems and the effect the structural features of interacting biomolecules have on the thermochemical parameters of diglycylglycine dissolution.

  11. An E-Health Solution for People With Alcohol Problems

    PubMed Central

    Gustafson, David H.; Boyle, Michael G.; Shaw, Bret R.; Isham, Andrew; McTavish, Fiona; Richards, Stephanie; Schubert, Christopher; Levy, Michael; Johnson, Kim

    2011-01-01

    Self-management of chronic diseases has been a research focus for years. Information and communication technologies (ICTs) have played a significant role in aiding patients and their families with that management task. The recent dramatic increase in smartphone capabilities has expanded the potential of these technologies by facilitating the integration of features specific to cell phones with advanced capabilities that extend the reach of what type of information can be assessed and which services can be provided. A recent review of the literature covering the use of ICTs in managing chronic diseases, including addiction, has examined the effectiveness of ICTs, with an emphasis on technologies tested in randomized controlled trials. One example of an addiction-relapse prevention system currently being tested is the Alcohol Comprehensive Health Enhancement Support System (A-CHESS) Program. PMID:23293549

  12. An e-health solution for people with alcohol problems.

    PubMed

    Gustafson, David H; Boyle, Michael G; Shaw, Bret R; Isham, Andrew; McTavish, Fiona; Richards, Stephanie; Schubert, Christopher; Levy, Michael; Johnson, Kim

    2011-01-01

    Self-management of chronic diseases has been a research focus for years. Information and communication technologies (ICTs) have played a significant role in aiding patients and their families with that management task. The recent dramatic increase in smartphone capabilities has expanded the potential of these technologies by facilitating the integration of features specific to cell phones with advanced capabilities that extend the reach of what type of information can be assessed and which services can be provided. A recent review of the literature covering the use of ICTs in managing chronic diseases, including addiction, has examined the effectiveness of ICTs, with an emphasis on technologies tested in randomized controlled trials. One example of an addiction-relapse prevention system currently being tested is the Alcohol Comprehensive Health Enhancement Support System (A-CHESS) Program. PMID:23293549

  13. SN1 reactions in supercritical carbon dioxide in the presence of alcohols: the role of preferential solvation.

    PubMed

    Delgado-Abad, Thais; Martínez-Ferrer, Jaime; Acerete, Rafael; Asensio, Gregorio; Mello, Rossella; González-Núñez, María Elena

    2016-07-01

    Ethanol () inhibits SN1 reactions of alkyl halides in supercritical carbon dioxide (scCO2) and gives no ethers as products. The unexpected behaviour of alcohols in the reaction of alkyl halides with 1,3-dimethoxybenzene () in scCO2 under different conditions is rationalised in terms of Brønsted and Lewis acid-base equilibria of reagents, intermediates, additives and products in a singular solvent characterised by: (i) the strong quadrupole and Lewis acid character of carbon dioxide, which hinders SN2 paths by strongly solvating basic solutes; (ii) the weak Lewis base character of carbon dioxide, which prevents it from behaving as a proton sink; (iii) the compressible nature of scCO2, which enhances the impact of preferential solvation on carbon dioxide availability for the solvent-demanding rate determining step. PMID:27303826

  14. Closantel nano-encapsulated polyvinyl alcohol (PVA) solutions.

    PubMed

    Vega, Abraham Faustino; Medina-Torres, Luis; Calderas, Fausto; Gracia-Mora, Jesus; Bernad-Bernad, MaJosefa

    2016-08-01

    The influence of closantel on the rheological and physicochemical properties (particle size and by UV-Vis absorption spectroscopy) of PVA aqueous solutions is studied here. About 1% PVA aqueous solutions were prepared by varying the closantel content. The increase of closantel content led to a reduction in the particle size of final solutions. All the solutions were buffered at pH 7.4 and exhibited shear-thinning behavior. Furthermore, in oscillatory flow, a "solid-like" type behavior was observed for the sample containing 30 μg/mL closantel. Indicating a strong interaction between the dispersed and continuous phases and evidencing an interconnected network between the nanoparticle and PVA, this sample also showed the highest shear viscosity and higher shear thinning slope, indicating a more intrincate structure disrupted by shear. In conclusion, PVA interacts with closantel in aqueous solution and the critical concentration for closantel encapsulation by PVA was about 30 μg/mL; above this concentration, the average particle size decreased notoriously which was associated to closantel interacting with the surface of the PVA aggregates and thus avoiding to some extent direct polymer-polymer interaction. PMID:26330226

  15. Polyelectrolyte and carbon nanotube multilayers made from ionic liquid solutions

    NASA Astrophysics Data System (ADS)

    Nakashima, Takuya; Zhu, Jian; Qin, Ming; Ho, Szushen; Kotov, Nicholas A.

    2010-10-01

    The inevitable contact of substrates with water during the traditional practice of layer-by-layer assembly (LBL) creates problems for multiple potential applications of LBL films in electronics. To resolve this issue, we demonstrate here the possibility of a LBL process using ionic liquids (ILs), which potentially eliminates corrosion and hydration processes related to aqueous media and opens additional possibilities in structural control of LBL films. ILs are also considered to be one of the best ``green'' processing solvents, and hence, are advantageous in respect to traditional organic solvents. Poly(ethyleneimine) (PEI) and poly(sodium styrenesulfonate) (PSS) were dispersed in a hydrophilic IL and successfully deposited in the LBL fashion. To produce electroactive thin films with significance to electronics, a similar process was realized for PSS-modified single-walled carbon nanotubes (SWNT-PSS) and poly(vinyl alcohol) (PVA). Characterization of the coating using standard spectroscopy and microscopy techniques typical of the multilayer field indicated that there are both similarities and differences in the structure and properties of LBL films build from ILs and aqueous solutions. The films exhibited electrical conductivity of 102 S m-1 with transparency as high as 98% for visible light, which is comparable to similar parameters for many carbon nanotube and graphene films prepared by both aqueous LBL and other methods.The inevitable contact of substrates with water during the traditional practice of layer-by-layer assembly (LBL) creates problems for multiple potential applications of LBL films in electronics. To resolve this issue, we demonstrate here the possibility of a LBL process using ionic liquids (ILs), which potentially eliminates corrosion and hydration processes related to aqueous media and opens additional possibilities in structural control of LBL films. ILs are also considered to be one of the best ``green'' processing solvents, and hence, are

  16. Reduction of Plutonium in Acidic Solutions by Mesoporous Carbons

    SciTech Connect

    Parsons-Moss, Tashi; Jones, Stephen; Wang, Jinxiu; Wu, Zhangxiong; Uribe, Eva; Zhao, Dongyuan; Nitsche, Heino

    2015-12-19

    Batch contact experiments with several porous carbon materials showed that carbon solids spontaneously reduce the oxidation state of plutonium in 1-1.5 M acid solutions, without significant adsorption. The final oxidation state and rate of Pu reduction varies with the solution matrix, and also depends on the surface chemistry and surface area of the carbon. It was demonstrated that acidic Pu(VI) solutions can be reduced to Pu(III) by passing through a column of porous carbon particles, offering an easy alternative to electrolysis with a potentiostat.

  17. Alcohol

    MedlinePlus

    ... as well as injuries, liver disease, heart disease, cancer, and other health problems. It can also cause problems at home, at work, and with friends. NIH: National Institute on Alcohol Abuse and Alcoholism

  18. Interaction of aromatic alcohols, aldehydes and acids with α-hydroxyl-containing carbon-centered radicals: A steady state radiolysis study

    NASA Astrophysics Data System (ADS)

    Samovich, S. N.; Brinkevich, S. D.; Shadyro, O. I.

    2013-01-01

    Benzaldehyde and its derivatives efficaciously oxidize in aqueous solutions α-hydroxyl-containing carbon-centered radicals (α-HCR) of various structures, suppressing thereby the radical recombination and fragmentation reactions. The compounds containing cinnamic moieties are capable of adding α-hydroxyethyl radicals (α-HER) to the carbon-carbon double bonds conjugated with the aromatic system to form molecular products identifiable by mass spectrometry. On radiolysis of aqueous ethanol solutions, reduction of α-HER by aromatic alcohols and acids has been shown to proceed via formation of their adducts with hydrated electron species.

  19. Alcoholism.

    ERIC Educational Resources Information Center

    Caliguri, Joseph P., Ed.

    This extensive annotated bibliography provides a compilation of documents retreived from a computerized search of the ERIC, Social Science Citation Index, and Med-Line databases on the topic of alcoholism. The materials address the following areas of concern: (1) attitudes toward alcohol users and abusers; (2) characteristics of alcoholics and…

  20. Barrier properties of poly(vinyl alcohol) membranes containing carbon nanotubes or activated carbon.

    PubMed

    Surdo, Erin M; Khan, Iftheker A; Choudhury, Atif A; Saleh, Navid B; Arnold, William A

    2011-04-15

    Carbon nanotube addition has been shown to improve the mechanical properties of some polymers. Because of their unique adsorptive properties, carbon nanotubes may also improve the barrier performance of polymers used in contaminant containment. This study compares the barrier performance of poly(vinyl alcohol) (PVA) membranes containing single-walled carbon nanotubes (SWCNTs) to that for PVA containing powdered activated carbon (PAC). Raw and surface-functionalized versions of each sorbent were tested for their abilities to adsorb 1,2,4-trichlorobenzene and Cu(2+), representing the important hydrophobic organic and heavy metal contaminant classes, as they diffused across the PVA. In both cases, PAC (for 1,2,4-trichlorobenzene) and functionalized PAC (for Cu(2+)) outperformed SWCNTs on a per mass basis by trapping more of the contaminants within the barrier membrane. Kinetics of sorption are important in evaluating barrier properties, and poor performance of SWCNT-containing membranes as 1,2,4-TCB barriers is attributed to kinetic limitations. PMID:21349636

  1. Gelation Behavior of 5-Chloro-8-hydroxyquinoline, an Antituberculosis Agent in Aqueous Alcohol Solutions

    PubMed Central

    Kolehmainen, Erkki; Salo, Hannu; Korpela, Jukka

    2012-01-01

    It was shown that 5-chloro-8-hydroxyquinoline, an antituberculosis agent, gels aqueous alcohol solutions efficiently. Thermal stability and gel-to-sol transition temperature of 1% gel in CD3OD/D2O (2:1) was studied by 1H-NMR. Fibrous structures of four xerogels have been characterized by scanning electron microscope. PMID:27029417

  2. Investigations on the predictability of the formation of glassy solid solutions of drugs in sugar alcohols.

    PubMed

    Langer, M; Höltje, M; Urbanetz, N A; Brandt, B; Höltje, H-D; Lippold, B C

    2003-02-18

    A prerequisite for the formation of glassy solid solutions prepared by the melting method is the miscibility of the respective drug and the carrier in the molten state. As could be shown experimentally, all investigated drug/sugar alcohol combinations miscible in the molten state form to some extent glassy solid solutions, dependent on their tendency to recrystallize during preparation. Therefore, the present study focuses on the evaluation of factors that govern the miscibility of molten drugs and sugar alcohols as carriers. In this context, solubility parameters are discussed as a means of predicting miscibility in comparison to a new approach, using calculated interaction parameters derived from molecular dynamics (MD) studies. There is evidence that a Coulomb interaction term C(SR), comprising short-range electrostatic interactions and hydrogen bonding energy is essential for the miscibility of drug and carrier in the molten state. To relate C(SR) to the molecular volume, a non-dimensional parameter P(i) is defined. For this parameter, a limiting value for miscibility exists. Contrary, calculated solubility parameter differences between drug and sugar alcohol in the range of 8-15 MPa(1/2) are not suitable for a prediction of miscibility or immiscibility, since the mixtures deviate from regular solution behavior. In irregular mixtures of drugs and sugar alcohols, an excess entropy and the formation of hydrogen bonds between unlike molecules favor miscibility, that cannot be predicted by regular solution theory. PMID:12550792

  3. Correlation Between Partial Pressure of Arterial Carbon Dioxide and End Tidal Carbon Dioxide in Patients with Severe Alcohol Withdrawal

    PubMed Central

    Yousuf, Tariq; Brinton, Taylor; Kramer, Jason; Khan, Basharath; Ziffra, Jeffrey; Villines, Dana; Shah, Poorvi; Hanif, Tabassum

    2015-01-01

    Background Respiratory depression is a common adverse effect of benzodiazepine administration to patients with severe alcoholic withdrawal. This study was conducted to assess the value of end tidal carbon dioxide (ETCO2) levels compared to partial pressure of arterial carbon dioxide (PaCO2) levels in monitoring respiratory depression secondary to benzodiazepine treatment in patients with severe alcohol withdrawal. Methods We retrospectively analyzed 36 patients admitted to the intensive care unit for severe alcohol withdrawal who had been administered sedative agents. Results We observed a statistically significant correlation between PaCO2 and ETCO2 at time 1 (r=0.74, P<0.01) and time 3 (r=0.52, P=0.02) but not at time 2 (r=0.22, P=0.31). Conclusion Our study confirms a positive correlation between PaCO2 and ETCO2 levels in patients experiencing severe alcohol withdrawal. PMID:26730226

  4. Formation of nanostructured solid-state carbon particles by laser ablation of graphite in isopropyl alcohol

    NASA Astrophysics Data System (ADS)

    Kitazawa, Sin-Iti; Abe, Hiroaki; Yamamoto, Shunya

    2005-02-01

    Nanostructured solid-state carbon particles with sizes of 1 10 μm are successfully formed from graphite target by applying laser ablation technique in isopropyl alcohol. In the laser ablation in liquid, the diffusion of the evaporated atomic carbon particles is prevented. It follows that the shock front is condensed in the high-density condition, and evaporated carbon particles are clustered and aggregated. Nanostructured solid-state carbon particles are formed by repeatedly gathering. In this study, the influence of laser ablation process on isopropyl alcohol solvent and graphite target is analyzed, and it is revealed that the possible influences on chemical reactions with isopropyl alcohol and the direct exfoliation from the target can be excluded in this condensation process.

  5. Continuous electrolytic decarbonation and recovery of a carbonate salt solution from a metal-contaminated carbonate solution.

    PubMed

    Kim, Kwang-Wook; Kim, Yeon-Hwa; Lee, Se-Yoon; Lee, Eil-Hee; Song, Kyusuk; Song, Kee-Chan

    2009-11-15

    This work studied the characteristic changes of a continuous electrolytic decarbonation and recovery of a carbonate salt solution from a metal-contaminated carbonate solution with changes of operational variables in an electrolytic system which consisted of a cell-stacked electrolyzer equipped with a cation exchange membrane and a gas absorber. The system could completely recover the carbonate salt solution from a uranyl carbonato complex solution in a continuous operation. The cathodic feed rate could control the carbonate concentration of the recovered solution and it affected the most transient pH drop phenomenon of a well type within the gas absorber before a steady state was reached, which caused the possibility of a CO(2) gas slip from the gas absorber. The pH drop problem could be overcome by temporarily increasing the OH(-) concentration of the cathodic solution flowing down within the gas absorber only during the time required for a steady state to be obtained in the case without the addition of outside NaOH. An overshooting peak of the carbonate concentration in the recovered solution before a steady state was observed, which was ascribed to the decarbonation of the initial solution filled within the stacked cells by a redundant current leftover from the complete decarbonation of the feeding carbonate solution. PMID:19604641

  6. Effect of sonication on the mechanical properties of poly (vinyl alcohol)/carbon nanotube composites

    NASA Astrophysics Data System (ADS)

    Truong, Van-Tan; Tsang, Kelly M. C.; Keough, Shannon J.; St John, Nigel A.

    2006-12-01

    Several sonication procedures were performed on multi-walled carbon nanotubes (MWNTs) in water by varying the length of time, the output power and the type of sonicating horn. Depending on the sonicating conditions, the multi-walled carbon nanotubes (MWNTs) could be well or poorly exfoliated and dispersed. Poly (vinyl alcohol) (PVA) and MNWT (0.5 wt%) composites were cast from the PVA/MWNT aqueous mixture. Enhancement of the mechanical properties of the composites was related to two factors: (1) crystallinity formed at the PVA and MWNT interface and (2) the size of nanotube agglomerates. The poorly dispersed solution produced nanotube agglomerates with the size of 50-100 μm that did not induce crystallization at the polymer/nanotube interface. They became stress concentrators reducing the Young's modulus and the tensile strength. Optimized sonication procedures resulted in well-dispersed nanotube agglomerates of submicron dimensions efficiently enhancing the mechanical properties. As centrifugation facilitated the removal of large agglomerates, noticeable enhancement of mechanical properties of the composites was achieved.

  7. Dissolution of Spent Nuclear Fuel in Carbonate-Peroxide Solution

    SciTech Connect

    Soderquist, Chuck Z.; Hanson, Brady D.

    2010-01-31

    This study shows that spent UO2 fuel can be completely dissolved in a carbonate-peroxide solution apparently without attacking the metallic Mo-Tc-Ru-Rh-Pd fission product phase. Samples of spent nuclear fuel were pulverized and sieved to a uniform size, then duplicate aliquots were weighed into beakers for analysis. One set was dissolved in near-boiling 10M nitric acid, and the other set was dissolved in a solution of ammonium carbonate and hydrogen peroxide at room temperature. All the resulting fuel solutions were then analyzed for Sr-90, Tc-99, Cs-137, plutonium, and Am-241. For all the samples, the concentrations of Cs-137, Sr-90, plutonium, and Am-241 were the same for both the nitric acid dissolution and the ammonium carbonate-hydrogen peroxide dissolution, but the technetium concentration of the ammonium carbonate-hydrogen peroxide fuel solution was only about 25% of the same fuels dissolved in hot nitric acid.

  8. Mechanism of sonochemical reduction of permanganate to manganese dioxide in aqueous alcohol solutions: Reactivities of reducing species formed by alcohol sonolysis.

    PubMed

    Okitsu, Kenji; Iwatani, Masaki; Okano, Koji; Uddin, Md Helal; Nishimura, Rokuro

    2016-07-01

    The sonochemical reduction of MnO4(-) to MnO2 in aqueous solutions was investigated as a function of alcohol concentration under Ar. The rate of MnO4(-) reduction initially decreased with increasing alcohol concentration, and then increased when the alcohol concentration was increased further. The concentrations at which the reduction rates were minimum depended on the hydrophobic properties of the added alcohols under ultrasonic irradiation. At low concentrations, the alcohols acted as OH radical scavengers; at high concentrations, they acted as reductant precursors: Rab, formed by abstraction reactions of the alcohols with sonochemically formed OH radicals or H atoms, and Rpy, formed by alcohol pyrolysis under ultrasonic irradiation. The results suggest that the reactivity order of the sonochemically formed reducing species with MnO4(-) at pH 7-9 is the sum of H2O2 and H>Rpy>Rab. The peak wavelengths of MnO2 colloidal solutions formed at high 1-butanol concentrations shifted to shorter wavelengths, suggesting the formation of small particles at high 1-butanol concentrations. The rates of sonochemical reduction of MnO2 to Mn(2+) in the presence of 1-butanol were slower than that in the absence of 1-butanol, because the sonochemical formation of H2O2 and H, which act as reductants, was suppressed by 1-butanol in aqueous solutions. PMID:26964972

  9. Poly(vinyl alcohol) Modified Porous Graphitic Carbon Stationary Phase for Hydrophilic Interaction Liquid Chromatography.

    PubMed

    Hou, Yanjie; Zhang, Feifang; Liang, Xinmiao; Yang, Bingcheng; Liu, Xiaodong; Dasgupta, Purnendu K

    2016-05-01

    We report a poly(vinyl alcohol) (PVA)-coated porous graphitic carbon (PGC, Hypercarb) packing as a novel stationary phase for hydrophilic interaction liquid chromatography (HILIC). The exterior and the pores of the PGC particles are coated with a thin layer of PVA by soaking the particles in a PVA solution, filtering, and thermally cross-linking the PVA. Such PVA coated PGC particles (5.7 μm diameter), hereinafter called PVA-PGC are stable at least through pH 1.0-12.7, can be made in <2 h, and exhibit different selectivity relative to six commercial HILIC phases and bare PGC. To our knowledge, this is the first fully pH-stable, completely neutral HILIC phase. Excellent efficiency stable is observed for polar analytes (∼70 000 and 118 000 plates/m for cytosine and resorcinol, respectively). Retention closely resembles standard HILIC behavior. Other substances can also be easily incorporated in the PVA layer; an anion exchange column can be readily made by incorporating diallyldimethylammonium chloride in the PVA coating solution. The ease of preparation without the requirement of synthetic skills or paraphernalia and the possibility of incorporating a variety of modifiers makes this a particularly versatile approach. PMID:27053418

  10. Thermodynamics of alcohols and monosaccharides in aqueous solutions of biuret at 25/sup 0/C

    SciTech Connect

    Barone, G.; Castronuovo, G.; Del Vecchio, P.; Elia, V.; Tosto, M.T.

    1988-10-01

    The excess enthalpies of ternary aqueous solutions of biuret with four aliphatic alcohols or four isomeric pentoses have been determined by flow microcalorimetry at 25/sup 0/C. The coefficients of the virial expansion of the excess enthalpies have been evaluated and compared with those already reported for urea and thiourea with the same alcohols and pentoses used here. For biuret-alcohol systems, the cross coefficients are positive and depend on the length and branching of the alkyl chain of the alcohols. On the contrary, they are negative for biuret-pentose systems. Hence, biuret, as urea and thiourea, is able to differentiate the behavior of families of solutes characterized by the same functional groups. The results are interpreted in terms of the relative stabilities of the hydration cospheres of predominantly hydrophobic or predominantly hydrophilic cosolutes. However, hypotheses about the hydration cospheres of the saccharides, which are more complex than those used previously, seem to be necessary to rationalize their complete behavior in water.

  11. The sporicidal activity and inactivation of chlorhexidine gluconate in aqueous and alcoholic solution.

    PubMed

    Gorman, S P; Jones, D S; Loftus, A M

    1987-08-01

    The sporicidal activity of chlorhexidine gluconate in aqueous and alcoholic solution against spores of Bacillus subtilis was examined over a broad temperature range. Activity was not observed at 20 degrees C even with concentrations as high as 10% chlorhexidine. Temperatures of 37 degrees-70 degrees C in combination with such high concentrations were required for reductions in spore viability. No viable spores were recoverable after 4 h contact at 55 degrees C with 10% aqueous chlorhexidine and none after 3 h contact with the alcoholic solution. Because of the high concentrations necessary for activity and the possibility of sporostasis occurring from inefficient chlorhexidine inactivation, existing inactivation systems were examined and modified to obtain satisfactory results. The spores of other Bacillus species examined (B. cereus, B. megaterium and B. stearothermophilus) proved to be considerably less resistant than those of B. subtilis. Presence of organic matter had little effect on the activity. PMID:3115938

  12. Catalytic conversion of alcohols having at least three carbon atoms to hydrocarbon blendstock

    DOEpatents

    Narula, Chaitanya K.; Davison, Brian H.

    2015-11-13

    A method for producing a hydrocarbon blendstock, the method comprising contacting at least one saturated acyclic alcohol having at least three and up to ten carbon atoms with a metal-loaded zeolite catalyst at a temperature of at least 100°C and up to 550°C, wherein the metal is a positively-charged metal ion, and the metal-loaded zeolite catalyst is catalytically active for converting the alcohol to the hydrocarbon blendstock, wherein the method directly produces a hydrocarbon blendstock having less than 1 vol % ethylene and at least 35 vol % of hydrocarbon compounds containing at least eight carbon atoms.

  13. Methods for sequestering carbon dioxide into alcohols via gasification fermentation

    DOEpatents

    Gaddy, James L; Ko, Ching-Whan; Phillips, J. Randy; Slape, M. Sean

    2013-11-26

    The present invention is directed to improvements in gasification for use with synthesis gas fermentation. Further, the present invention is directed to improvements in gasification for the production of alcohols from a gaseous substrate containing at least one reducing gas containing at least one microorganism.

  14. Hydrodynamics and oxygen mass transfer in a packed bed split-cylinder airlift reactor containing dilute alcoholic solutions

    NASA Astrophysics Data System (ADS)

    Keshavarz Moraveji, Mostafa; Ebrahimi Fakhari, Mona; Mohsenzadeh, Elmira; Davarnejad, Reza

    2013-01-01

    In this article, the influences of alcohols on the hydrodynamics and oxygen mass transfer characteristics in an airlift reactor equipped with packing were investigated. The hydrodynamic parameters and mass transfer coefficient in 1 % (v/v) aqueous solutions of four aliphatic alcohols were tested. It was concluded that alcohols addition increased gas holdup and gas-liquid mass transfer coefficient. The packing installation increased mass transfer coefficient, gas holdup and liquid circulation velocity, as well.

  15. Alcohol.

    ERIC Educational Resources Information Center

    Schibeci, Renato

    1996-01-01

    Describes the manufacturing of ethanol, the effects of ethanol on the body, the composition of alcoholic drinks, and some properties of ethanol. Presents some classroom experiments using ethanol. (JRH)

  16. Quantum conductance steps in solutions of multiwalled carbon nanotubes.

    PubMed

    Urbina, A; Echeverría, I; Pérez-Garrido, A; Díaz-Sánchez, A; Abellán, J

    2003-03-14

    We have prepared solutions of multiwalled carbon nanotubes in Aroclor 1254, a mixture of polychlorinated biphenyls. The solutions are stable at room temperature. Transport measurements were performed using a scanning-tunneling probe on a sample prepared by spin coating the solution on gold substrates. Conductance steps were clearly seen. A histogram of a high number of traces shows maximum peaks at integer values of the conductance quantum G(0)=2e(2)/h, demonstrating ballistic transport at room temperature along the carbon nanotube over distances longer than 1.4 microm. PMID:12689021

  17. Using Micromechanical Resonators to Measure Rheological Properties and Alcohol Content of Model Solutions and Commercial Beverages

    PubMed Central

    Paxman, Rosemary; Stinson, Jake; Dejardin, Anna; McKendry, Rachel A.; Hoogenboom, Bart W.

    2012-01-01

    Micromechanic resonators provide a small-volume and potentially high-throughput method to determine rheological properties of fluids. Here we explore the accuracy in measuring mass density and viscosity of ethanol-water and glycerol-water model solutions, using a simple and easily implemented model to deduce the hydrodynamic effects on resonating cantilevers of various length-to-width aspect ratios. We next show that these measurements can be extended to determine the alcohol percentage of both model solutions and commercial beverages such as beer, wine and liquor. This demonstrates how micromechanical resonators can be used for quality control of every-day drinks. PMID:22778654

  18. Catalytic activity of carbon nanotubes in the conversion of aliphatic alcohols

    NASA Astrophysics Data System (ADS)

    Zhitnev, Yu. N.; Tveritinova, E. A.; Chernyak, S. A.; Savilov, S. V.; Lunin, V. V.

    2016-06-01

    Carbon nanotubes (CNTs) obtained via the catalytic pyrolysis of hexane at 750°C were studied as the catalysts in conversion of C2-C4 alcohols. The efficiency of CNTs as catalysts in dehydration and dehydrogenation of ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, and tert-butanol was studied by means of pulse microcatalysis. The surface and structural characteristics of CNTs are investigated via SEM, TEM, DTA, BET, and XPS. CNTs are shown to be effective catalysts in the conversion of alcohols and do not require additional oxidative treatment. The regularities of the conversion of aliphatic alcohols, related to the properties of the CNTs surface and the structure of the alcohols are identified.

  19. Solution behavior of metoclopramide in aqueous-alcoholic solutions at 30°C

    NASA Astrophysics Data System (ADS)

    Deosarkar, S. D.; Sawale, R. T.; Tawde, P. D.; Kalyankar, T. M.

    2016-07-01

    Densities (ρ) and refractive indices ( n D) of solutions of antiemetic drug metoclopramide (4-amino-5-chloro- N-(2-(diethylamino)ethyl)-2-methoxybenzamide hydrochloride hydrate) in methanolwater and ethanol-water mixtures of different compositions were measured at 30°C. Apparent molar volume (φv) of the drug was calculated from density data and partial molar volumes (φ v 0 ) were determined from Massons relation. Concentration dependence of nD has been studied to determine refractive indices of solution at infinite dilution ( n D 0 ). Results have been interpreted in terms of solute-solvent interactions.

  20. Multivariate Curve Resolution Methods Illustrated Using Infrared Spectra of an Alcohol Dissolved in Carbon Tetrachloride

    ERIC Educational Resources Information Center

    Grung, Bjorn; Nodland, Egil; Forland, Geir Martin

    2007-01-01

    The analysis of the infrared spectra of an alcohol dissolved in carbon tetrachloride gives a better understanding of the various multivariate curve resolution methods. The resulting concentration profile is found to be very useful for calculating the degree of association and equilibrium constants of different compounds.

  1. Surface-oxidized carbon black as a catalyst for the water oxidation and alcohol oxidation reactions.

    PubMed

    Suryanto, Bryan H R; Zhao, Chuan

    2016-05-11

    Carbon black (CB) is popularly used as a catalyst support for metal/metal oxide nanoparticles due to its large surface area, excellent conductivity and stability. Herein, we show that surface oxidized CB itself, after acidic treatment and electrochemical oxidation, exhibits significant catalytic activity for the electrochemical oxidation of water and alcohols. PMID:27097802

  2. Divisive effect of alcohol-water mixed solvents on growth morphology of calcium carbonate crystals.

    PubMed

    Zhang, Li; Yue, Lin-Hai; Wang, Fei; Wang, Qi

    2008-08-28

    Controlling the process of crystal growth is of importance to the biomineralization and materials science. In this work, some novel morphology of calcium carbonate (CaCO3) was precipitated in an ethanol-water binary solvent (EWBS) with a CaCl2/Na2CO3 reaction system. For the solutions of CaCl2/Na2CO3 in EWBS, the alcoholization and hydration of Ca2+ and CO3(2-) were discussed from the radial distribution functions by molecular dynamics simulations, and the number density profiles of water molecules around and approximately 15 A away from CO3(2-) were employed to reveal the distribution of water molecules. It is found that EWBS has a divisive effect on Ca2+ and CO3(2-), and the local inhomogeneity of EWBS would be enhanced by adding some Na2CO3 into it. This inhomogeneity results in an aqueous two-phase system as x E goes up to 0.7. In addition, the novel morphology of CaCO3 under different molar ratios of Ca2+/CO3(2-) and in different mixed solvents were confirmed by XRD and SEM, and the relationships between the morphology of CaCO 3 and the structural properties of mixed solvents were further explored. PMID:18681476

  3. Electroreduction of carbon dioxide in aqueous solutions at metal electrodes

    SciTech Connect

    Augustynski, J.; Jermann, B.; Kedzierzawski, P.

    1996-12-31

    The quantities of carbon stored in the form of atmospheric carbon dioxide, CO{sub 2} in the hydrosphere and carbonates in the terrestrial environment substantially exceed those of fossil fuels. In spite of this the industrial use of carbon dioxide as a source of chemical carbon is presently limited to preparation of urea and certain carboxylic acids as well as organic carbonates and polycarbonates. However, the situation is expected to change in the future, if effective catalytic systems allowing to activate carbon dioxide will become available. In this connection, the electrochemical reduction of CO{sub 2}, requiring only an additional input of water and electrical energy, appears as an attractive possibility. For more than 100 years formic acid and formates of alkali metals were considered as the only significant products of the electroreduction of carbon dioxide in aqueous solutions. The highest current efficiencies, exceeding 90 %, were obtained either with mercury or with amalgam electrodes. The only comprehensive study regarding kinetics of CO{sub 2} reduction in aqueous solution has been performed by Eyring et al. using a mercury cathode. This paper describes electrolysis studies.

  4. Viscosities of cetylpyridinium bromide solutions (aqueous and aqueous KBr) in the presence of alcohols and amines

    SciTech Connect

    David, S.L.; Kumar, S.; Kabir-ud-Din

    1997-01-01

    Among the large number of additives, alcohols hold a special place, being by far the most common cosurfactants which are added to surfactant-oil combinations to generate microemulsions. Though the studies using amines as cosurfactant in microemulsions are few, it has been proved that they are also potential candidates for such formulations. The effect of organic additives (aliphatic/aromatic amines or alcohols) on the viscosities of aqueous and 0.1 M KBr solutions of 0.05 or 0.1 M cetylpyridinium bromide have been measured under Newtonian flow conditions. The viscosity changed dramatically in the presence of KBr. This is explained by the favorable conditions produced by the salt which assists the micellar growth by organic additives with a concomitant enhancement in viscosity. Reasons for the effectiveness of these additives are suggested. The causes of the viscosity decrease at higher concentrations of the additive are also explained.

  5. Effect of extraction solutions on carbonation of cementitious materials in aqueous solutions.

    PubMed

    Jo, Hwanju; Jo, Ho Young; Jang, Young-Nam

    2012-06-01

    Carbonation efficiency was evaluated for three cementitious materials having different CaO-bearing minerals (lime, Portland cement and waste concrete) using various extraction reagents (HCl, CH3COOH, NH4Cl and deionized water). The cementitious materials were subjected to Ca extraction and carbonation tests under ambient pressure and temperature conditions. The Ca extraction efficiency generally decreased in the order lime, Portland cement and waste concrete, regardless of the extraction solution. Among the extraction solutions, NH4Cl was the most effective for Ca extraction and carbonation. The results of this study suggest that the types of extraction solution and CaO-bearing mineral of the materials are primary factors affecting carbonation efficiency. PMID:22856314

  6. Thermodynamics of trivalent lanthanide and actinide elements in carbonate solutions

    SciTech Connect

    Rao, L.; Rai, D.; Felmy, A.R.; Fulton, R.W.

    1995-12-01

    Knowledge of the thermodynamics of actinide and lanthanide elements in various aqueous electrolyte solutions is essential for the development of actinide separation techniques. It is particularly important to understand the thermodynamics of these elements in basic and concentrated electrolyte solutions if the separation techniques are in concentrated electrolytes and to be applied to the treatment of nuclear wastes, since many of these wastes contain concentrated electrolytes and are under strongly basic conditions. Solubility experiments were conducted for neodymium(III) in bicarbonate and carbonate solutions. Experimental results were analyzed with the specific ion-interaction approach of Pitzer. A thermodynamic model was developed to describe the solubilities of corresponding carbonate compounds of neodymium(III) and americium(III) under wide ranges of pH and carbonate concentrations.

  7. Supercharging with m-nitrobenzyl alcohol and propylene carbonate: forming highly charged ions with extended, near-linear conformations.

    PubMed

    Going, Catherine C; Williams, Evan R

    2015-04-01

    The effectiveness of the supercharging reagents m-nitrobenzyl alcohol (m-NBA) and propylene carbonate at producing highly charged protein ions in electrospray ionization is compared. Addition of 5% m-NBA or 15% propylene carbonate increases the average charge of three proteins by ∼21% or ∼23%, respectively, when these ions are formed from denaturing solutions (water/methanol/acetic acid). These results indicate that both reagents are nearly equally effective at supercharging when used at their optimum concentrations. A narrowing of the charge state distribution occurs with both reagents, although this effect is greater for propylene carbonate. Focusing the ion signal into fewer charge states has the advantage of improving sensitivity. The maximum charge state of ubiquitin formed with propylene carbonate is 21+, four charges higher than previously reported. Up to nearly 30% of all residues in a protein can be charged, and the collisional cross sections of the most highly charged ions of both ubiquitin and cytochrome c formed with these supercharging reagents were measured for the first time and found to be similar to those calculated for theoretical highly extended, linear or near-linear conformations. Under native supercharging conditions, m-NBA is significantly more effective at producing high charge states than propylene carbonate. PMID:25719488

  8. Thermodynamics of micelle formation in a water-alcohol solution of sodium tetradecyl sulfate

    NASA Astrophysics Data System (ADS)

    Shilova, S. V.; Tret'yakova, A. Ya.; Barabanov, V. P.

    2016-01-01

    The effects of addition of ethanol and propan-1-ol on sodium tetradecyl sulfate micelle formation in an aqueous solution are studied via microprobe fluorescence microscopy and conductometry. The critical micelle concentration, quantitative characteristics of micelles, and thermodynamic parameters of micelle formation are determined. Addition of 5-15 vol % of ethanol or 5-10 vol % of propan-1-ol is shown to result in a lower critical micelle concentration than in the aqueous solution, and in the formation of mixed spherical micelles whose sizes and aggregation numbers are less than those for the systems without alcohol. The contribution from the enthalpy factor to the free energy of sodium tetradecyl sulfate micelle formation is found to dominate in mixed solvents, in contrast to aqueous solutions.

  9. Phase transition of carbonate solvent mixture solutions at low temperatures

    NASA Astrophysics Data System (ADS)

    Okumura, Takefumi; Horiba, Tatsuo

    2016-01-01

    The phase transition of carbonate solvent mixture solutions consisting of ethylene carbonate (EC), dimethyl carbonate (DMC), ethyl methyl carbonate (EMC), and LiPF6 salt have been studied for improving the low temperature performance of lithium-ion batteries. The Li ion conductivity at 25 °C was maximum at x = 0.3 in a series of 1 M LiPF6 mixed carbonate solvents compositions consisting of ECxDMC0.5-0.5xEMC0.5-0.5x (x = 0 to 0.6), while the maximum tended to shift to x = 0.2 as the temperature lowered. The differential scanning calorimetry results showed that the freezing temperature depressions of EC in the 1 M LiPF6 solution were larger than those of the DMC or EMC. The chemical shift of 7Li nuclear magnetic resonance changed from a constant to increasing at around x = 0.3, which could be reasonably understood by focusing on the change in solvation energy calculated using Born equation. However, in the region of a high EC concentration of over x = 0.3 (EC/LiPF6 > 4) in the 1 M LiPF6 solution, the free EC from the solvation to the lithium ions seems to reduce the freezing temperature depression of the EC, and thus, decreases the ionic conductivity of the solution at low temperatures, due to the EC freezing.

  10. Adsorptive removal of antibiotics from aqueous solution using carbon materials.

    PubMed

    Yu, Fei; Li, Yong; Han, Sheng; Ma, Jie

    2016-06-01

    Antibiotics, an important type of environmental contamination, have attracted many researchers to the study of their removal from aqueous solutions. Adsorption technology is a fast, efficient, and economical physicochemical method that is extensively used in wastewater treatment. From original activated carbon and carbon nanotubes to the latest graphene-based materials, carbon-based materials have been widely used as highly effective adsorbents for contaminant removal from aqueous solution because of their large specific surface area, high porosity, and high reaction activity. In this article, adsorption removal methods for four major types of antibiotic (tetracyclines, sulfonamides, macrolides, and quinolones) are reviewed. We also provide an overview of the application development of carbon materials as adsorbents for antibiotic removal from aqueous solution. The most promising works are discussed, and the main challenges in preparing high-performance adsorbents and the development tendency of adsorbents are also analyzed. This work provides theoretical guidance for subsequent research in the design and modification of carbon materials for applications in the adsorption removal of antibiotics from aqueous solution. PMID:27031800

  11. Observations on the Solubility of Skeletal Carbonates in Aqueous Solutions.

    PubMed

    Chave, K E; Deffeyes, K S; Weyl, P K; Garrels, R M; Thompson, M E

    1962-07-01

    Carbonate skeletal materials of marine organisms exhibit a wide range of solubilities in aqueous solutions. In most cases, the dissolution of the carbonate mineral is irreversible and therefore the material can have no true equilibrium solubility. Relative solubilities have been measured in distilled water and in sea water. The least soluble mineral appears to be calcite with low magnesium content; the most soluble is calcite containing 20 to 30 percent MgCO(3) in solid solution. Aragonite has an intermediate solubility. PMID:17774123

  12. Modeling Corrosion Reactions of Steel in a Dilute Carbonate Solution

    NASA Astrophysics Data System (ADS)

    Eliyan, Faysal Fayez; Alfantazi, Akram

    2016-02-01

    This research models the corrosion reactions of a high-strength steel in an aerated, dilute, carbonate solution during a single-cycle voltammetry. Based on a previous study (Eliyan et al. in J Mater Eng Perform 24(6):1-8, 2015) and a literature survey, the corrosion reactions of the cathodic reduction, anodic dissolution, and passivation, as well as the interfacial interactions and the chemistry of the corrosion products are illustrated in schematics. The paper provides a visual guide on the corrosion reactions for steel in carbonate solutions based on the available mechanistic details that were reported and are still being investigated in literature.

  13. Carbon-Nanotubes-Supported Pd Nanoparticles for Alcohol Oxidations in Fuel Cells: Effect of Number of Nanotube Walls on Activity.

    PubMed

    Zhang, Jin; Lu, Shanfu; Xiang, Yan; Shen, Pei Kang; Liu, Jian; Jiang, San Ping

    2015-09-01

    Carbon nanotubes (CNTs) are well known electrocatalyst supports due to their high electrical conductivity, structural stability, and high surface area. Here, we demonstrate that the number of inner tubes or walls of CNTs also have a significant promotion effect on the activity of supported Pd nanoparticles (NPs) for alcohol oxidation reactions of direct alcohol fuel cells (DAFCs). Pd NPs with similar particle size (2.1-2.8 nm) were uniformly assembled on CNTs with different number of walls. The results indicate that Pd NPs supported on triple-walled CNTs (TWNTs) have the highest mass activity and stability for methanol, ethanol, and ethylene glycol oxidation reactions, as compared to Pd NPs supported on single-walled and multi-walled CNTs. Such a specific promotion effect of TWNTs on the electrocatalytic activity of Pd NPs is not related to the contribution of metal impurities in CNTs, oxygen-functional groups of CNTs or surface area of CNTs and Pd NPs. A facile charge transfer mechanism via electron tunneling between the outer wall and inner tubes of CNTs under electrochemical driving force is proposed for the significant promotion effect of TWNTs for the alcohol oxidation reactions in alkaline solutions. PMID:25900368

  14. Carbon composites with metal nanoparticles for Alcohol fuel cells

    NASA Astrophysics Data System (ADS)

    Ventrapragada, Lakshman; Siddhardha, R. S.; Podilla, Ramakrishna; Muthukumar, V. S.; Creager, Stephen; Rao, A. M.; Ramamurthy, Sai Sathish

    2015-03-01

    Graphene due to its high surface area and superior conductivity has attracted wide attention from both industrial and scientific communities. We chose graphene as a substrate for metal nanoparticle deposition for fuel cell applications. There are many chemical routes for fabrication of metal-graphene composites, but they have an inherent disadvantage of low performance due to the usage of surfactants, that adsorb on their surface. Here we present a design for one pot synthesis of gold nanoparticles and simultaneous deposition on graphene with laser ablation of gold strip and functionalized graphene. In this process there are two natural advantages, the nanoparticles are synthesized without any surfactants, therefore they are pristine and subsequent impregnation on graphene is linker free. These materials are well characterized with electron microscopy to find their morphology and spectroscopic techniques like Raman, UV-Vis. for functionality. This gold nanoparticle decorated graphene composite has been tested for its electrocatalytic oxidation of alcohols for alkaline fuel cell applications. An electrode made of this composite showed good stability for more than 200 cycles of operation and reported a low onset potential of 100 mV more negative, an important factor for direct ethanol fuel cells.

  15. Electrical behavior of polymer hydrogel composed of poly(vinyl alcohol)/hyaluronic acid in solution

    NASA Astrophysics Data System (ADS)

    Kim, Seon Jeong; Yoon, Seoung Gil; Park, Sang Jun; Lee, Chang Kee; Shin, Su Ryon; Lee, Young Moo; Kim, In Young; Kim, Sun I.

    2003-07-01

    Interpenetrating polymer networks (IPN) composed of poly(vinyl alcohol) (PVA) and hyaluronic acid (HA) were prepared and exhibited electrical sensitive behavior. The swelling behavior of the PVA/HA IPN was studied by immersion of the gel in aqueous NaCl solutions at various concentrations and pHs. Also, the stimuli response of the PVA/HA IPN in electric fields was investigated. When swollen IPN was placed between a pair of electrodes, the PVA/HA IPN exhibited bending behavior upon the application of an electric field. The PVA/HA IPN also showed stepwise bending behavior depending on the electric stimulus. Also, for using biomedical application, the bending behavior of PVA/HA IPN has been studied in hank"s solution at pH 7.4

  16. Direct electrochemistry of alcohol oxidase using multiwalled carbon nanotube as electroactive matrix for biosensor application.

    PubMed

    Das, Madhuri; Goswami, Pranab

    2013-02-01

    Rapid detection of alcohol is important in clinical diagnosis and fermentation industry. An octameric alcohol oxidase (AOx) (Mr 675 kDa) from Pichia pastoris, immobilized on multiwalled carbon nanotubes-Nafion® (MWCNT-Nf) matrix and encapsulated with polyethylenimine (PEI) on gold electrode (AuE), showed a redox peak at 0.21V (vs. Ag/AgCl electrode at pH 7.5) for oxidation of alcohol. The electron transfer rate constant and surface coverage of the immobilized AOx were 1.69±0.15 s⁻¹ and 2.43×10⁻¹² mol cm⁻², respectively. Studies on response and kinetics of Au-MWCNT-Nf-AOx-PEI bioelectrodes for alcohol showed a linear response in the range of 8 μM-42 μM, response time of 55 s for steady state current, and detection limit of 5 μM. The bioelectrode retains ~90% of the original response even after four weeks when stored in potassium phosphate buffer pH 7.5 at 4 °C. The fabricated bioelectrode was found to exclude interference caused by the common electroactive species such as ascorbic acid, uric acid, lactic acid, glucose and urea. The bioelectrode also showed reliable response characteristics in blood serum samples. The findings of the investigation have established the direct electrochemistry of the AOx protein and its potential biosensor application for quantitative detection of alcohol in blood serum. PMID:23000393

  17. Synthesis and characterization of polyvinyl alcohol based multiwalled carbon nanotube nanocomposites

    NASA Astrophysics Data System (ADS)

    Malikov, E. Y.; Muradov, M. B.; Akperov, O. H.; Eyvazova, G. M.; Puskás, R.; Madarász, D.; Nagy, L.; Kukovecz, Á.; Kónya, Z.

    2014-07-01

    Multiwalled carbon nanotubes were synthesized by chemical vapor deposition over an Fe-Co/alumina catalyst. Nanotubes were then oxidized and grafted with polyvinyl alcohol (PVA). The obtained nanostructure was characterized by Raman spectroscopy, XRD, FTIR, EDX, SEM, TEM and TGA methods. FTIR confirmed the presence of the characteristic peaks of the anticipated ester group. The formation of polymer nanocomposites based on polyvinyl alcohol and multiwalled carbon nanotubes was confirmed by SEM and TEM. High resolution electron micrographs revealed that the primary binding sites for PVA grafting are the sidewall defects of the nanotubes. The novelty of this work is the use of the Fischer esterification reaction for creating the permanent link between the nanotubes and the PVA matrix.

  18. The performance of a surface-applied corrosion inhibitor for the carbon steel in saturated Ca(OH){sub 2} solutions

    SciTech Connect

    Zheng, Haibing; Li, Weihua; Ma, Fubin; Kong, Qinglin

    2014-01-15

    In the present work, the performance of an amino alcohol based surface applied inhibitor was studied by the electrochemical techniques in saturated Ca(OH){sub 2} solutions. The surface morphology of the carbon steel was observed by scanning electron microscope, and the energy diffraction spectrum was also tested. Results showed that the inhibitor used in this work demonstrated obvious inhibition efficiency on the carbon steel in saturated Ca(OH){sub 2} solutions. The inhibition mechanism of the inhibitor lies in the quick adsorption of the active component on carbon steel surface.

  19. Study the density, ultrasonic and compressibility of binary mixture of aqueous solution of isopropyl alcohol and mustard oil

    NASA Astrophysics Data System (ADS)

    Monupal, Suthar, B.

    2016-05-01

    The ultrasonic velocities, compressibility and bulk modulus of binary mixtures of aqueous solution of isopropyl alcohol with mustard oil have been measured at different concentrations at room temperature. The results are varied with the concentration in such a way i.e. ultrasonic velocity and Bulk Modulus is decreases with the increase in concentration and compressibility is increases with the increase in concentration of aqueous isopropyl alcohol. It is due to molecular interactions present in the mixtures.

  20. Hydrogenolysis of 5-carbon sugars, sugar alcohols, and methods of making propylene glycol

    DOEpatents

    Werpy, Todd A [West Richland, WA; Zacher, Alan H [Kennewick, WA

    2006-05-02

    Methods and compositions for reactions of hydrogen over a Re-containing catalyst with compositions containing a 5-carbon sugar, sugar alcohol, or lactic acid are described. It has been surprisingly discovered that reaction with hydrogen over a Re-containing multimetallic catalyst resulted in superior conversion and selectivity to desired products such as propylene glycol. A process for the synthesis of PG from lactate or lactic acid is also described.

  1. Hydrogenolysis Of 5-Carbon Sugars, Sugar Alcohols And Compositions For Reactions Involving Hydrogen

    SciTech Connect

    Werpy, Todd A.; Frye, Jr., John G.; Zacher, Alan H.; Miller, Dennis J.

    2004-01-13

    Methods and compositions for reactions of hydrogen over a Re-containing catalyst with compositions containing a 5-carbon sugar, sugar alcohol, or lactic acid are described. It has been surprisingly discovered that reaction with hydrogen over a Re-containing multimetallic catalyst resulted in superior conversion and selectivity to desired products such as propylene glycol. A process for the synthesis of PG from lactate or lactic acid is also described.

  2. Hydrogenolysis of 5-carbon sugars, sugar alcohols, and other methods and compositions for reactions involving hydrogen

    SciTech Connect

    Werpy, Todd A; Zacher, Alan H

    2002-11-12

    Methods and compositions for reactions of hydrogen over a Re-containing catalyst with compositions containing a 5-carbon sugar, sugar alcohol, or lactic acid are described. It has been surprisingly discovered that reaction with hydrogen over a Re-containing multimetallic catalyst resulted in superior conversion and selectivity to desired products such as propylene glycol. A process for the synthesis of PG from lactate or lactic acid is also described.

  3. Microkinetic Modeling of Benzyl Alcohol Oxidation on Carbon-Supported Palladium Nanoparticles

    DOE PAGESBeta

    Savara, Aditya; Rossetti, Ilenia; Chan-Thaw, Carine E.; Prati, Laura; Villa, Alberto

    2016-07-14

    Six products are formed from benzyl alcohol oxidation over Pd nanoparticles using O2 as the oxidant: benzaldehyde, toluene, benzyl ether, benzene, benzoic acid, and benzyl benzoate. Three experimental parameters were varied here: alcohol concentration, oxygen concentration, and temperature. Microkinetic modeling using a mechanism published recently with surface intermediates was able to produce all 18 trends observed experimentally with mostly quantitative agreement. Approximate analytical equations derived from the microkinetic model for isothermal conditions reproduced the isothermal trends and provided insight. The most important activation energies are Ea2=57.9 kJ mol₋1, Ea5=129 kJ mol₋1, and Ea6=175 kJ mol₋1, which correspond to alcohol dissociation,more » alkyl hydrogenation, and the reaction of alkyl species with alkoxy species. Upper limits for other activation energies were identified. The concepts of a sticking coefficient and steric factor in solution were applied.« less

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

    PubMed

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

    2002-07-01

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

  5. Simultaneous leaching and carbon sequestration in constrained aqueous solutions

    SciTech Connect

    Phelps, Tommy Joe; Moon, Ji Won; Roh, Yul; Cho, Kyu Seong

    2011-01-01

    The behavior of metal ions leaching and precipitated mineral phases of metal-rich fly ash (FA) was examined in order to evaluate microbial impacts on carbon sequestration and metal immobilization. The leaching solutions consisted of aerobic deionized water (DW) and artificial eutrophic water (AEW) that was anaerobic, organic- and mineral-rich, and higher salinity as is typical of bottom water in eutrophic algae ponds. The Fe- and Ca-rich FAs were predominantly composed of quartz, mullite, portlandite, calcite, hannebachite, maghemite, and hematite. After 86 days, only Fe and Ca contents exhibited a decrease in leaching solutions while other major and trace elements showed increasing or steady trends in preference to the type of FA and leaching solution. Ca-rich FA showed strong carbon sequestration efficiency ranging up to 32.3 g CO(2)/kg FA after 86 days, corresponding to almost 65% of biotic carbon sequestration potential under some conditions. Variations in the properties of FAs such as chemical compositions, mineral constituents as well as the type of leaching solution impacted CO(2) capture. Even though the relative amount of calcite increased sixfold in the AEW and the relative amount of mineral phase reached 37.3 wt% using Ca-rich FA for 86 days, chemical sequestration did not accomplish simultaneous precipitation and sequestration of several heavy metals.

  6. Simultaneous leaching and carbon sequestration in constrained aqueous solutions.

    PubMed

    Moon, Ji-Won; Cho, Kyu-Seong; Moberly, James G; Roh, Yul; Phelps, Tommy J

    2011-12-01

    The behavior of metal ions' leaching and precipitated mineral phases of metal-rich fly ash (FA) was examined in order to evaluate microbial impacts on carbon sequestration and metal immobilization. The leaching solutions consisted of aerobic deionized water (DW) and artificial eutrophic water (AEW) that was anaerobic, organic- and mineral-rich, and higher salinity as is typical of bottom water in eutrophic algae ponds. The Fe- and Ca-rich FAs were predominantly composed of quartz, mullite, portlandite, calcite, hannebachite, maghemite, and hematite. After 86 days, only Fe and Ca contents exhibited a decrease in leaching solutions while other major and trace elements showed increasing or steady trends in preference to the type of FA and leaching solution. Ca-rich FA showed strong carbon sequestration efficiency ranging up to 32.3 g CO(2)/kg FA after 86 days, corresponding to almost 65% of biotic carbon sequestration potential under some conditions. Variations in the properties of FAs such as chemical compositions, mineral constituents as well as the type of leaching solution impacted CO(2) capture. Even though the relative amount of calcite increased sixfold in the AEW and the relative amount of mineral phase reached 37.3 wt% using Ca-rich FA for 86 days, chemical sequestration did not accomplish simultaneous precipitation and sequestration of several heavy metals. PMID:21246259

  7. A carbon nanotube-infused polysulfone membrane with polyvinyl alcohol layer for treating oil-containing waste water

    PubMed Central

    Maphutha, Selby; Moothi, Kapil; Meyyappan, M.; Iyuke, Sunny E.

    2013-01-01

    A carbon nanotube (CNT) integrated polymer composite membrane with a polyvinyl alcohol barrier layer has been prepared to separate oil from water for treatment of oil-containing waste water. The CNTs were synthesised using chemical vapour deposition, and a phase inversion method was employed for the blending of the CNTs in the polymer composite solution for casting of the membrane. Relative to the baseline polymer, an increase of 119% in the tensile strength, 77% in the Young's modulus and 258% in the toughness is seen for a concentration of 7.5% CNTs in the polymer composite. The permeate through the membrane shows oil concentrations below the acceptable 10 mg/L limit with an excellent throughput and oil rejection of over 95%. PMID:23518875

  8. Radiation preparation of graphene/carbon nanotubes hybrid fillers for mechanical reinforcement of poly(vinyl alcohol) films

    NASA Astrophysics Data System (ADS)

    Ma, Hui-Ling; Zhang, Long; Zhang, Youwei; Wang, Shuojue; Sun, Chao; Yu, Hongyan; Zeng, Xinmiao; Zhai, Maolin

    2016-01-01

    Graphene/carbon nanotubes (G/CNTs) hybrid fillers were synthesized by γ-ray radiation reduction of graphene oxide (GO) in presence of CNTs. The obtained hybrid fillers with three-dimensional (3D) interconnected network structure were characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM). Poly(vinyl alcohol) (PVA) composite films with enhanced mechanical properties and thermal stability were subsequently prepared by solution blending of G/CNTs with PVA matrix. The tensile strength and Young's modulus of PVA composite films containing 1 wt% G/CNTs were measured to be 81.9 MPa and 3.9 GPa respectively, which were 56% and 33.6% higher than those of pure PVA. These substantial improvements could be attributed to the interconnected 3D structure of G/CNTs, homogeneous dispersion as well as the strong hydrogen-bonding interaction between G/CNTs and PVA macromolecular chains.

  9. Mechanisms of diphylline release from dual-solute loaded poly(vinyl alcohol) matrices.

    PubMed

    Hasimi, Albana; Papadokostaki, Kyriaki G; Sanopoulou, Merope

    2014-01-01

    The release kinetics of the model hydrophilic drug, diphylline (DPL), from physically crosslinked poly(vinyl alcohol) (PVA) matrices, is studied in relation to the drug load and the presence of a second solute incorporated in the matrix. The second solute, a gadolinium (III) complex (Gd-DTPA), is a commonly used MRI contrast agent. The water uptake kinetics by the glassy PVA matrix was found to deviate from t(1/2) law and to occur on time scales comparable to those of diphylline release. The corresponding rate of diphylline release was found to be substantially stabilized as compared to a purely diffusion-controlled release process, in line with theoretical predictions under conditions of relaxation-controlled water uptake kinetics. The release rate of DPL was found (i) to increase with increasing DPL load and (ii) for a particular DPL load, to increase in the presence of Gd-DTPA, incorporated in the matrix. The results were interpreted on the basis of the diphylline-induced plasticization of the polymer (evidenced by the depression of Tg) and of the excess hydration of the matrix at high solute loads. The latter effect was found to be additive in the case of dual-solute loaded matrices. PMID:24268271

  10. Vitamin C hinders radiation cross-linking in aqueous poly(vinyl alcohol) solutions

    NASA Astrophysics Data System (ADS)

    Oral, Ebru; Bodugoz-Senturk, Hatice; Macias, Celia; Muratoglu, Orhun K.

    2007-12-01

    Poly(vinyl alcohol) (PVA) is a promising semi-crystalline material for biomedical applications. It is soluble in water and can be formed into hydrogels by freezing and thawing or crystallizing from an aqueous theta solution such as that of polyethylene glycol (PEG). Radiation cross-linking caused by sterilization or high dose irradiation of concentrated PVA solutions could compromise some properties of these hydrogels. Therefore, we hypothesized that radiation cross-linking of PVA solutions and PVA-PEG theta gels could be prevented by using the antioxidant vitamin C as an anticross-linking agent. Our hypothesis tested positive. Vitamin C concentrations of 0.75 and 4.5 mol/mol of PVA repeating unit could prevent cross-linking in 17.5 wt/v% PVA solutions made with PVA molecular weight of 115,000 g/mol irradiated to 25 and 100 kGy, respectively. Vitamin C also prevented cross-linking in 25 kGy irradiated PVA-PEG theta gels containing up to 5 wt% PEG and decreased the viscosity of those up to 39 wt%.

  11. Carbon monoxide bioconversion to butanol-ethanol by Clostridium carboxidivorans: kinetics and toxicity of alcohols.

    PubMed

    Fernández-Naveira, Ánxela; Abubackar, Haris Nalakath; Veiga, María C; Kennes, Christian

    2016-05-01

    Butanol production from carbon monoxide-rich waste gases or syngas is an attractive novel alternative to the conventional acetone-butanol-ethanol (ABE) fermentation. Solvent toxicity is a key factor reported in ABE fermentation with carbohydrates as substrates. However, in the gas-fermentation process, kinetic aspects and the inhibition effect of solvents have not thoroughly been studied. Therefore, different batch bottle experiments were carried out with the bacterial species Clostridium carboxidivorans using CO as carbon source for butanol-ethanol fermentation. A maximum specific growth rate of 0.086 ± 0.004 h(-1) and a biomass yield of 0.011 gbiomass/gCO were found, which is significantly lower than in other clostridia grown on sugars. Besides, three assays were carried out to check the inhibitory effect of butanol, ethanol, and their mixtures. Butanol had a higher inhibitory effect on the cells than ethanol and showed a lower IC50, reduced growth rate, and slower CO consumption with increasing alcohol concentrations. A concentration of 14-14.50 g/L butanol caused 50 % growth inhibition in C. carboxidivorans, and 20 g/L butanol resulted in complete inhibition, with a growth rate of 0 h(-1). Conversely, 35 g/L ethanol decreased by 50 % the final biomass concentration respect to the control and yielded the lowest growth rate of 0.024 h(-1). The inhibitory effect of mixtures of both alcohols was also checked adding similar, near identical, concentrations of each one. Growth decreased by 50 % in the presence of a total concentration of alcohols of 16.22 g/L, consisting of similar amounts of each alcohol. Occasional differences in initially added concentrations of alcohols were minimal. The lowest growth rate (0.014 h(-1)) was observed at the highest concentration assayed (25 g/L). PMID:26921183

  12. Phosphoryloxymethyl carbamates and carbonates--novel water-soluble prodrugs for amines and hindered alcohols.

    PubMed

    Safadi, M; Oliyai, R; Stella, V J

    1993-09-01

    Phosphoryloxymethyl carbonates and carbamates of the type R1R2X-CO-O-CH2-O-PO3(-2) (X = O or N) were evaluated as potentially novel water-soluble collapsible prodrugs for alcohols and amines. These were prepared by reaction of alpha-chloromethyl chloroformate with the starting alcohol or amine to give the corresponding alpha-chloromethyl carbonate or carbamate, respectively. Reaction with silver dibenzyl phosphate followed by debenzylation by hydrogenolysis gave the desired products. The aqueous chemical stability of the phosphoryloxymethylcarbonyl derivatives of 2-indanol (3a), beta-(3,4-dimethoxyphenyl)ethylamine (3b), and benzocaine (3c) were evaluated. The aqueous hydrolysis of 3a-3c resulted in regeneration of the parent alcohol or amines. As expected, the hydrolytic behaviors of these derivatives were found to differ from that of simple alkyl and aryl phosphomonoesters. The rates of hydrolysis were extremely rapid, with the dianionic phosphate species possessing a higher reactivity than the monoanionic species. This was attributed to the proximity of the phosphate group to the carbonyl moiety. The carbamate derivatives, 3b and 3c, displayed greater chemical stability compared to the carbonate derivative, 3a. Alkaline phosphatases-mediated hydrolysis of the phosphate ester bond in 3c led to a rapid cascade reaction resulting in regeneration of the parent amine, benzocaine. Although the alcohol derivative described here appeared to be too chemically unstable to be ideal as a prodrug, the derivatives of the amines might have some use. They are expected to be cleaved in vivo by alkaline phosphatases. PMID:8234176

  13. Sorption of cobalt on activated carbons from aqueous solutions

    SciTech Connect

    Paajanen, A.; Lehto, J.; Santapakka, T.; Morneau, J.P.

    1997-01-01

    The efficiencies of 15 commercially available activated carbons were tested for the separation of trace cobalt ({sup 60}Co) in buffer solutions at pH 5.0, 6.7, and 9.1. On the basis of the results four carbon products, Diahope-006, Eurocarb TN5, Hydraffin DG47, and Norit ROW Supra, were selected for further study. These carbons represented varying (low, medium and high) cobalt removal efficiencies and were prepared of three typical raw materials: peat, coconut shell, or coal. Study was made of the effects on sorption efficiencies of factors of interest in metal/radionuclide-bearing waste effluents. These factors were pH, sodium ions, borate, and citrate.

  14. Frequency dependence of electron spin-lattice relaxation for semiquinones in alcohol solutions

    NASA Astrophysics Data System (ADS)

    Elajaili, Hanan B.; Biller, Joshua R.; Eaton, Sandra S.; Eaton, Gareth R.

    2014-10-01

    The spin-lattice relaxation rates at 293 K for three anionic semiquinones (2,5-di-t-butyl-1,4-benzosemiquinone, 2,6-di-t-butyl-1,4-benzosemiquinone, and 2,3,5,6-tetramethoxy-1,4-benzosemiquinone) were studied at up to 8 frequencies between 250 MHz and 34 GHz in ethanol or methanol solution containing high concentrations of OH-. The relaxation rates are about a factor of 2 faster at lower frequencies than at 9 or 34 GHz. However, in perdeuterated alcohols the relaxation rates exhibit little frequency dependence, which demonstrates that the dominant frequency-dependent contribution to relaxation is modulation of dipolar interactions with solvent nuclei. The relaxation rates were modeled as the sum of two frequency-independent contributions (spin rotation and a local mode) and two frequency-dependent contributions (modulation of dipolar interaction with solvent nuclei and a much smaller contribution from modulation of g anisotropy). The correlation time for modulation of the interaction with solvent nuclei is longer than the tumbling correlation time of the semiquinone and is consistent with hydrogen bonding of the alcohol to the oxygen atoms of the semiquinones.

  15. Dialkyl pyridinedicarboxylates` extraction ability toward copper(II) from chloride solutions and its modification with alcohols

    SciTech Connect

    Bogacki, M.B.; Jakubiak, A.; Szymanowski, J.; Cote, G.

    1997-03-01

    Dipentyl pyridinedicarboxylates (denoted hereafter as L) with different positions of the ester groups were synthesized and used for copper(II) extraction from chloride solutions containing up to 10 mol/L Cl{sup {minus}}. The effect of decanol addition on copper extraction was studied. A molecular modeling technique was used to estimate the structures of extractants, copper complexes, and associates with alcohol. It was found that the ability of pyridinecarboxylates to extract copper depends on the aqueous phase composition and the position of the ester groups in the pyridine ring. All the investigated compounds except dipentyl pyridine-2,6-dicarboxylate extract copper(II) by formation of CuCl{sub 2}L{sub 2} complexes. Dipentyl pyridine-2,6-dicarboxylate forms another type of complex, probably CuCl{sub 2}L. However, this compound is not suitable for copper extraction as its copper complex precipitates. Dipentyl pyridine-3,5-dicarboxylate was found to be the most suitable extractant among the various compounds listed. Finally it is shown that the possibilities to modify the extraction ability of pyridinecarboxylates with a hydrophobic alcohol such as decanol are relatively weak. Some enhancement was, however, observed when 20% of decanol was added to the organic phase containing dipentyl pyridine-3,5-dicarboxylate.

  16. Insights into non-Fickian solute transport in carbonates

    PubMed Central

    Bijeljic, Branko; Mostaghimi, Peyman; Blunt, Martin J

    2013-01-01

    [1] We study and explain the origin of early breakthrough and long tailing plume behavior by simulating solute transport through 3-D X-ray images of six different carbonate rock samples, representing geological media with a high degree of pore-scale complexity. A Stokes solver is employed to compute the flow field, and the particles are then transported along streamlines to represent advection, while the random walk method is used to model diffusion. We compute the propagators (concentration versus displacement) for a range of Peclet numbers (Pe) and relate it to the velocity distribution obtained directly on the images. There is a very wide distribution of velocity that quantifies the impact of pore structure on transport. In samples with a relatively narrow spread of velocities, transport is characterized by a small immobile concentration peak, representing essentially stagnant portions of the pore space, and a dominant secondary peak of mobile solute moving at approximately the average flow speed. On the other hand, in carbonates with a wider velocity distribution, there is a significant immobile peak concentration and an elongated tail of moving fluid. An increase in Pe, decreasing the relative impact of diffusion, leads to the faster formation of secondary mobile peak(s). This behavior indicates highly anomalous transport. The implications for modeling field-scale transport are discussed. Citation: Bijeljic, B., P. Mostaghimi, and M. J. Blunt (2013), Insights into non-Fickian solute transport in carbonates, Water Resour. Res., 49, 2714–2728, doi:10.1002/wrcr.20238. PMID:24223444

  17. Pressure effect on water dynamics in tert-butyl alcohol/water solutions

    NASA Astrophysics Data System (ADS)

    Calandrini, Vania; Deriu, Antonio; Onori, Giuseppe; Paciaroni, Alessandro; Telling, Mark T. F.

    2006-09-01

    We report here a quasi-elastic neutron scattering (QENS) investigation of the effect of pressure on the diffusivity properties of water in a dilute aqueous solution of hydrophobic molecules (tert-butyl alcohol, TBA). The experiment was performed at fixed TBA concentration (0.02 molar fraction) by varying pressure from 1 to 2000 bar at two different temperatures (268 and 278 K). The quasi-elastic line-shapes have been analysed in terms of a model based on the memory function formalism. Our data indicate that, on increasing pressure up to 2000 bar, the diffusion coefficient of water in the TBA/water mixture exhibits a relative increase larger than that of pure water under the same thermodynamic conditions. The extent of this effect increases with decreasing temperature. The observed behaviour is described in terms of pressure-induced distortions of the H-bonded random network of liquid water.

  18. Radiolytic formation of Ag clusters in aqueous polyvinyl alcohol solution and hydrogel matrix

    NASA Astrophysics Data System (ADS)

    Kumar, Manmohan; Varshney, Lalit; Francis, Sanju

    2005-05-01

    Ag+ ions, in aqueous polyvinyl alcohol (PVA) solution and in PVA hydrogel matrix have been gamma radiolytically reduced to produce Ag clusters. UV-visible absorption spectral characteristics of Ag clusters obtained under different gamma dose, Ag+ concentration, PVA concentration and crosslinking density of the gel used have been studied. The effect of Ag+ ions on the radiation crosslinking of the PVA chains, have also been investigated by viscosity measurements. The radiation-induced Ag+ ion reduction was followed by crosslinking of the PVA chains. PVA was found to be a very efficient stabilizer to prevent aggregation of Ag clusters. The clusters produced in the hydrogel matrix were expected to be smaller than the pore size (∼2-20 nm) of the gels used in the study. These Ag clusters were unable to reduce methyl viologen (MV2+) chloride and were stable in air.

  19. Dissolution and mechanical behaviors of recrystallized carbamazepine from alcohol solution in the presence of additives

    NASA Astrophysics Data System (ADS)

    Nokhodchi, A.; Bolourtchian, N.; Dinarvand, R.

    2005-02-01

    Carbamazepine (CBZ) crystals were grown from pure ethanol solutions containing various additives (PEG 4000, PVP K30 or Tween 80). Physical characteristics of the crystals were studied for the morphology of crystals using scanning electron microscope, for the identification of polymorphism by X-ray powder diffraction (XRPD) and FT-IR, and for thermodynamic properties using differential scanning calorimetery (DSC). The dissolution behaviour of various carbamazepine crystals was also studied by dissolution apparatus II at pH 7.4 containing 1% sodium lauryl sulphate (SLS). The scanning electron micrograph (SEM) studies showed that the presence of the additives in the solutions growth medium affected the morphology and size of carbamazepine crystals. SEMs of untreated and treated carbamazepine crystals obtained from alcohol containing PEG 4000, PVP K30 or Tween 80 showed that the crystal shape of untreated carbamazepine is flaky or thin plate-like, whereas the crystals obtained from alcohol containing no additive, PEG 4000, PVP K30 or Tween 80 are polyhedral prismatic, block-shaped, polyhedral or hexagonal, respectively. XRPD, FT-IR and DSC results showed that the untreated CBZ was form III and recrystallization of CBZ in the absence or presence of the additives did not cause any polymorphic changes. The results showed that the higher dissolution rate and compact strength were observed for the crystals obtained in the presence of PVP K30. The presence of the additives in crystallization medium alters crystal morphology of carbamazepine, but only the samples crystallized in the presence of PVP K30 showed an improvement in dissolution rate and tensile strength.

  20. Direct growth of nanocrystalline graphitic carbon films on BaF2 by alcohol CVD

    NASA Astrophysics Data System (ADS)

    Tan, Yan; Nakamura, Atsushi; Kubono, Atsushi

    2016-03-01

    Multilayered nanocrystalline graphitic carbon films were directly formed on BaF2 substrates by the alcohol chemical vapor deposition method using ethanol. Domain size was typically 46 nm as estimated from the peak intensity ratios of G- and D-band of the Raman spectra, which were higher than currently reported values for various dielectric substrates. Sheet resistance measured by the four-probe method was 900 Ω/sq. A possible formation mechanism of the graphitic carbon layer was discussed referring to the results of X-ray photoelectron spectroscopy (XPS) and energy dispersive X-ray spectroscopy (EDX) for a composition analysis. It was found that the graphitic carbon layers were formed on the BaO surface, which was produced by the oxidization of the BaF2 substrate by the ethanol source.

  1. MICROWAVE-ASSISTED SYNTHESIS OF CROSSLINKED POLY(VINYL ALCOHOL) NANOCOMPOSITES COMPRISING SINGLE-WALLED CARBON NANOTUBES, MULTI-WALLED CARBON NANOTUBES AND BUCKMINSTERFULLERENE

    EPA Science Inventory

    We report a facile method to accomplish cross-linking reaction of poly (vinyl alcohol) (PVA) with single-wall carbon nanotubes (SWNT), multi-wall carbon nanotubes (MWNT), and Buckminsterfullerene (C-60) using microwave (MW) irradiation. Nanocomposites of PVA cross-linked with SW...

  2. Mesoporous Carbon Supported Rh Nanoparticle Catalysts for the Production of C2+ Alcohol from Syngas.

    PubMed

    Kim, Min-Ji; Kim, Tae-Wan; Chae, Ho-Jeong; Kim, Chul-Ung; Jeong, Soon-Yong; Kim, Jeong-Rang; Ha, Kyoung-Su

    2016-02-01

    Uniform rhodium nanoparticles (NP) with three different particle sizes (1.9, 2.4, and 3.6 nm) were prepared via a polyol method with rhodium (III) acetylacetonate, poly(vinylpyrrolidone) with different concentrations of sodium citrate. The prepared Rh nanoparticles were impregnated into the ordered mesoporous carbon supports with two different pore structures (2D hexagonal and 3D cubic). The prepared Rh nanoparticle-supported ordered mesoporous carbons (OMCs) were introduced as catalysts for the CO hydrogenation of syngas to produce C2 higher alcohols. The characteristics of the Rh nanoparticle-supported ordered mesoporous carbons catalysts were analyzed through transmission electron microscopy, powder X-ray diffraction, and N2 physisorption analysis. The catalytic tests of the catalyst were performed using a fixed-bed reactor. The results revealed that the catalysts exhibited the different catalytic activity and selectivity of higher alcohols, which could be attributed to the different OMC structures, the nanoparticle size of Rh, and aggregation of Rh nanoparticles during the reaction. PMID:27433718

  3. Influence of the composition of isopropyl alcohol/water mixture solvents in catalyst ink solutions on proton exchange membrane fuel cell performance

    NASA Astrophysics Data System (ADS)

    Ngo, Trung Truc; Yu, T. Leon; Lin, Hsiu-Li

    2013-03-01

    We study the morphology of Nafion in the dilute IPA (isopropyl alcohol)/water mixture solutions containing 20-100 wt.% of IPA and in the Pt-C/Nafion gas diffusion electrodes (GDEs; where Pt-C is the carbon powder deposited on its surface with Pt particles), which are prepared by spraying on the carbon paper surfaces with a layer of Pt-C, Nafion and IPA/water ink solution. The fuel cell performance of the GDEs strongly depends on the Nafion morphology in the ink solutions. A lower IPA content in the Pt-C/Nafion ink solutions results in the formation of larger and higher negatively charged Nafion aggregated particles, which leads to higher steric hindrance of the deposition of Nafion ionomer on the surface of Pt-C particles and thus a thinner Nafion film in contact on the Pt-C particle surfaces. The thinner Nafion film in contact with the Pt particles in the CL increases the chances of the Pt particles in contact with the H2/O2 gas, leading to a higher fuel cell performance.

  4. Fluidic delivery of homogeneous solutions through carbon tube bundles

    NASA Astrophysics Data System (ADS)

    Srikar, R.; Yarin, A. L.; Megaridis, C. M.

    2009-07-01

    A wide array of technological applications requires localized high-rate delivery of dissolved compounds (in particular, biological ones), which can be achieved by forcing the solutions or suspensions of such compounds through nano or microtubes and their bundled assemblies. Using a water-soluble compound, the fluorescent dye Rhodamine 610 chloride, frequently used as a model drug release compound, it is shown that deposit buildup on the inner walls of the delivery channels and its adverse consequences pose a severe challenge to implementing pressure-driven long-term fluidic delivery through nano and microcapillaries, even in the case of such homogeneous solutions. Pressure-driven delivery (3-6 bar) of homogeneous dye solutions through macroscopically-long (~1 cm) carbon nano and microtubes with inner diameters in the range 100 nm-1 µm and their bundled parallel assemblies is studied experimentally and theoretically. It is shown that the flow delivery gradually shifts from fast convection-dominated (unobstructed) to slow jammed convection, and ultimately to diffusion-limited transport through a porous deposit. The jamming/clogging phenomena appear to be rather generic: they were observed in a wide concentration range for two fluorescent dyes in carbon nano and microtubes, as well as in comparable transparent glass microcapillaries. The aim of the present work is to study the physics of jamming, rather than the chemical reasons for the affinity of dye molecules to the tube walls.

  5. Supercritical carbon dioxide, a new medium for aerobic alcohol oxidations catalysed by copper-TEMPO.

    PubMed

    Herbert, Matthew; Montilla, Francisco; Galindo, Agustín

    2010-01-21

    The copper catalysed aerobic oxidation of selected alcohol substrates in supercritical carbon dioxide (scCO(2)), employing a range of simple copper(II) catalyst compounds, is here described. The copper acetate complex of polydimethylsiloxane (PDMS) functionalised pyridine (1), compound 2, has previously been synthesised and characterised by us and its solubility in scCO(2) demonstrated. Due to this solubility we anticipated that the selective aerobic oxidation of alcohols to aldehydes could be homogeneously catalysed by this compound in scCO(2) in combination with the co-catalyst 2,2,6,6-tetramethylpiperidin-1-yloxy free radical (TEMPO). Our initial results showed that complete oxidation of 4-nitrobenzyl alcohol was achieved within 4 h of reaction. However, the activities of analogous copper derivatives containing simpler pyridine substituents, [Cu(AcO)(2)(py)](2) and [Cu(AcO)(2)(4VP)](2) (4VP = 4-vinylpyridine), were shown to be similar, in spite of their negligible solubility in scCO(2). When we repeated the reactions in highly non-polar hexane rather than scCO(2) similar observations were made. In both cases, as 2 is soluble and the pyridine analogues are not, a much higher reaction rate was anticipated for 2 as it is the only compound capable of homogeneous catalysis. However, in some cases slightly better activities were observed for [Cu(AcO)(2)(py)](2) rather than for the PDMS functionalised analogue, 2. Thus, despite poor catalyst solubility typically being very inhibitory in this type of catalytic process, in this system solubilisation of the catalyst is not necessary. In continuation the activity of silica supported copper complexes was therefore investigated. Employing such catalysts the 4-nitrobenzyl and benzyl alcohol substrates were completely oxidised to the corresponding aldehydes in scCO(2), this time employing lower catalyst loadings. Other types of alcohol substrate showed more limited conversions however. To conclude, alcohol oxidation in the non

  6. carbonate solid solution at high pressures up to 55 GPa

    NASA Astrophysics Data System (ADS)

    Spivak, Anna; Solopova, Natalia; Cerantola, Valerio; Bykova, Elena; Zakharchenko, Egor; Dubrovinsky, Leonid; Litvin, Yuriy

    2014-09-01

    Magnesite, siderite and ferromagnesites Mg1- x Fe x CO3 ( x = 0.05, 0.09, 0.2, 0.4) were characterized using in situ Raman spectroscopy at high pressures up to 55 GPa. For the Mg-Fe-carbonates, the Raman peak positions of six modes (T, L, ν4, ν1, ν3 and 2ν2) in the dependence of iron content in the carbonates at ambient conditions are presented. High-pressure Raman spectroscopy shows that siderite undergoes a spin transition at ~40 GPa. The examination of the solid solutions with compositions Mg0.6Fe0.4CO3, Mg0.8Fe0.2CO3, Mg0.91Fe0.09CO3 and Mg0.95Fe0.05CO3 indicates that with increase in the amount of the Fe spin transition pressure increases up to ~45 GPa.

  7. Carbon nitride for the selective oxidation of aromatic alcohols in water under visible light.

    PubMed

    Long, Baihua; Ding, Zhengxin; Wang, Xinchen

    2013-11-01

    The selective oxidation of aromatic alcohols in water is achieved by using a carbon nitride (CN) catalyst, dioxygen, and visible light. The unique electronic structure of CN avoids the direct formation of hydroxyl radicals, which typically cause the total oxidation of organics. The chemical stability of CN allows several chemical protocols for photoredox catalysis in water, as exemplified by cooperative catalysis involving Brønsted acids. This leads to a new, green pathway for diverse organic transformations using sunlight and water. PMID:24039175

  8. Effect of Hydroxyl Concentration on Chemical Sensitivity of Polyvinyl Alcohol/Carbon-Black Composite Chemiresistors

    SciTech Connect

    Hughes, Robert C.; Patel, Sanjay V.; Yelton, W. Graham

    1999-05-19

    The sensitivity and selectivity of polyvinyl alcohol (PVA) / carbon black composite films have been found to vary depending upon the hydroxylation percentage ("-OH") of the polymer. These chemiresistors made from PVA films whose polymer backbone is 88% hydroxylated (PVA88) have a high sensitivity to water, while chemiresistors made from PVA75 have a higher sensitivity to methanol. The minor differences in polymer composition result in films with different Hildebrand volubility parameters. The relative responses of several different PVA-based chemiresistors to solvents with different volubility parameters are presented. In addition, polyvinyl acetate (PVAC) films with PVA88 are used in an array to distinguish the responses to methanol-water mixtures.

  9. Catalytic ozonation of pentachlorophenol in aqueous solutions using granular activated carbon

    NASA Astrophysics Data System (ADS)

    Asgari, Ghorban; Samiee, Fateme; Ahmadian, Mohammad; Poormohammadi, Ali; solimanzadeh, Bahman

    2014-11-01

    The efficiency of granular activated carbon (GAC) was investigated in this study as a catalyst for the elimination of pentachlorophenol (PCP) from contaminated streams in a laboratory-scale semi-batch reactor. The influence of important parameters including solution pH (2-10), radical scavenger (tert-butanol, 0.04 mol/L), catalyst dosage (0.416-8.33 g/L), initial PCP concentration (100-1000 mg/L) and ozone flow rate (2.3-12 mg/min) was examined on the efficiency of the catalytic ozonation process (COP) in degradation and mineralization of PCP in aqueous solution. The experimental results showed that catalytic ozonation with GAC was most effective at pH of 8 with ozone flow rate of 12 mg/min and a GAC dosage of 2 g. Compared to the sole ozonation process (SOP), the removal levels of PCP and COP were, 98, and 79 %, respectively. The degradation rate of kinetics was also investigated. The results showed that using a GAC catalyst in the ozonation of PCP produced an 8.33-fold increase in rate kinetic compared to the SOP under optimum conditions. Tert-butanol alcohol (TBA) was used as a radical scavenger. The results demonstrated that COP was affected less by TBA than by SOP. These findings suggested that GAC acts as a suitable catalyst in COP to remove refractory pollutants from aqueous solution.

  10. Solution Spinning and Characterization of Poly (vinyl alcohol) /Soybean Polyblend Fibers

    NASA Astrophysics Data System (ADS)

    Zhang, Xiefei; Kumar, Satish

    2002-03-01

    Solution Spinning and Characterization of Poly (vinyl alcohol) /Soybean Polyblend Fibers Xiefei Zhang and Satish Kumar School of Textile and Fiber Engineering Georgia Institute of Technology Atlanta GA 30032 During 1930s and 40s there was significant research activity in processing fibers from regenerated proteins. However, due to development of synthetic fibers and partially due to low tensile strength of the regenerated protein fibers, there has not been much interest in this field over last half a century. To improve strength of the regenerated protein, an attempt has been made to process PVA /soybean protein polyblend fibers. PVA/Soybean protein ratio of 100/0, 90/10, 70/30, 50/50, 40/60, 20/80 and 0/100 have been utilized. This has been done in an attempt to take advantage of the PVA/soybean interaction. Urea, sodium sulfite, as well as heat, were used to make denatured soybean protein solution, which was suitable for solution spinning. The polyblend fibers underwent post-spinning treatment, such as crosslinking, washing, drying and heat treatment. The fibers have been characterized for thermal behavior and tensile as well as dynamic mechanical properties. Blend fiber morphology was studied using scanning electron microscopy and fiber structure characterized using wide angle X-ray diffraction. Effects of draw ratio, crosslinking time, crosslinking agent, heat treatment conditions as well as PVA/soybean composition on the mechanical properties of polyblend fibers have been studied. Dynamic mechanical analysis as well as scanning electron microscopy exhibit PVA /soybean protein compatibility.

  11. Mechanism for benzyl alcohol-induced aggregation of recombinant human interleukin-1 receptor antagonist in aqueous solution.

    PubMed

    Zhang, Ye; Roy, Shouvik; Jones, Latoya S; Krishnan, Sampathkumar; Kerwin, Bruce A; Chang, Byeong S; Manning, Mark C; Randolph, Theodore W; Carpenter, John F

    2004-12-01

    Benzyl alcohol, an antimicrobial preservative, accelerates aggregation and precipitation of recombinant human interleukin-1 receptor antagonist (rhIL-1ra) in aqueous solution. The loss of native monomer during incubation at 37 degrees C was determined by analysis of sample aliquots with size exclusion high performance liquid chromatography (SE-HPLC). Benzyl alcohol caused minor perturbation of the tertiary structure of the protein without changing its secondary structure, documenting that the preservative caused a minor shift in the protein molecular population toward partially unfolded species. Consistent with this conclusion, in the presence of benzyl alcohol the rate of H-D exchange was accelerated and the fluorescence of 1-anilinonaphthalene-8-sulfonic acid in the presence of rhIL1ra was increased. Benzyl alcohol did not alter the free energy of unfolding based on unfolding experiments in urea or guanidine HCl. With differential scanning calorimetry it was determined that benzyl alcohol reduced the apparent Tm of rhIL-1ra, but this effect occurred because the preservative lowered the temperature at which the protein aggregated during heating. Isothermal calorimetry documented that the interaction of benzyl alcohol with rhIL-1ra is relatively weak and hydrophobically driven. Thus, benzyl alcohol accelerates protein aggregation by binding to the protein and favoring an increase in the level of partially unfolded, aggregation-competent species. Sucrose partially inhibited benzyl alcohol-induced aggregation and tertiary structural change. Sucrose is preferentially excluded from the surface of the protein, favoring most compact native state species over expanded aggregation-prone forms. PMID:15514986

  12. Enhanced mechanical properties and morphological characterizations of poly(vinyl alcohol) carbon nanotube composite films

    NASA Astrophysics Data System (ADS)

    Chen, Wei; Tao, Xiaoming; Xue, Pu; Cheng, Xiaoyin

    2005-12-01

    Tensile tests were carried out on free-standing composite films of poly(vinyl alcohol) (PVA) and multiwall carbon nanotubes (MWNTs) for different loading levels. Results show that overall mechanical properties of the composite were greatly improved as compared to the neat PVA film. For PVA-based materials at significant high loading level such as 9.1 wt.% MWNTs, considerable increases in Young's modulus, tensile strength and toughness by factors of 4.5, 2.7 and 4.1, respectively, were achieved. Raman, SEM, TEM, and DSC techniques were used to evaluate the PVA/MWNTs composite system. Strong acid-modification of the pristine MWNTs and the subsequent ultrasonication processing allowed good distribution of the nanotubes in the matrix. SEM together with DSC result shows apparent good wetting of the nanotubes by the PVA matrix, which are supportive of good interfacial bonding between the modified carbon nanotubes and the hosting polymer matrix.

  13. Dispersion of denatured carbon nanotubes by using a dimethylformamide solution

    NASA Astrophysics Data System (ADS)

    Thuy Nguyen, Thi; Uan Nguyen, Sy; Tam Phuong, Dinh; Chien Nguyen, Duc; Mai, Anh Tuan

    2011-09-01

    The dispersion of carbon nanotubes (CNTs) in liquid plays an important role in fundamental research and applied science. The most common technique applied to disperse CNTs is ultrasonication. The surfactants used for CNT dispersion are ethanol, sodium dodecyl benzenesulfonate (SDBS), dodecyltrimethylammonium bromide (DATB), sodium dodecyl sulfate (SDS) and sodium dodecylbenzene sulfonate (NaDDBS). This paper presents the dispersion of denatured CNTs by using a dimethylformamide (DMF) solution. The DMF is adsorbed on the surface of the nanotubes by a hydrophobic or π–π interaction. Ultrasonication helps DMF debundle the nanotubes by Coulombic or hydrophilic interaction, allowing the Van der Waals forces among the individual nanotubes to be overcome. UV–Vis spectra of dispersed CNTs in solution showed a maximum at 260 nm and decreased from UV to near IR. The vibration properties of the carbon samples were characterized with Raman spectroscopy, which illustrated the D and G bands of denatured CNTs at 1354 and 1581 cm‑1, respectively, different from the values of 1352 cm‑1 and 1580 cm‑1, respectively, for undenatured CNTs. Finally, the interaction between surfactants and nanotubes was studied by Fourier transform infrared spectroscopy (FTIR).

  14. Insights into non-Fickian solute transport in carbonates

    NASA Astrophysics Data System (ADS)

    Bijeljic, Branko; Mostaghimi, Peyman; Blunt, Martin J.

    2013-05-01

    We study and explain the origin of early breakthrough and long tailing plume behavior by simulating solute transport through 3-D X-ray images of six different carbonate rock samples, representing geological media with a high degree of pore-scale complexity. A Stokes solver is employed to compute the flow field, and the particles are then transported along streamlines to represent advection, while the random walk method is used to model diffusion. We compute the propagators (concentration versus displacement) for a range of Peclet numbers (Pe) and relate it to the velocity distribution obtained directly on the images. There is a very wide distribution of velocity that quantifies the impact of pore structure on transport. In samples with a relatively narrow spread of velocities, transport is characterized by a small immobile concentration peak, representing essentially stagnant portions of the pore space, and a dominant secondary peak of mobile solute moving at approximately the average flow speed. On the other hand, in carbonates with a wider velocity distribution, there is a significant immobile peak concentration and an elongated tail of moving fluid. An increase in Pe, decreasing the relative impact of diffusion, leads to the faster formation of secondary mobile peak(s). This behavior indicates highly anomalous transport. The implications for modeling field-scale transport are discussed.

  15. Aggregation in dilute aqueous tert-butyl alcohol solutions: Insights from large-scale simulations

    NASA Astrophysics Data System (ADS)

    Gupta, Rini; Patey, G. N.

    2012-07-01

    Molecular dynamics simulations employing up to 64 000 particles are used to investigate aggregation and microheterogeneity in aqueous tert-butyl alcohol (TBA) solutions for TBA mole fractions Xt ⩽ 0.1. Four different force fields are considered. It is shown that the results obtained can be strongly dependent on the particular force field employed, and can be significantly influenced by system size. Two of the force fields considered show TBA aggregation in the concentration range Xt ≈ 0.03 - 0.06. For these models, systems of 64 000 particles are minimally sufficient to accommodate the TBA aggregates. The structures resulting from TBA aggregation do not have a well-defined size and shape, as one might find in micellar systems, but are better described as TBA-rich and water-rich regions. All pair correlation functions exhibit long-range oscillatory behavior with wavelengths that are much larger than molecular length scales. The oscillations are not strongly damped and the correlations can easily exceed the size of the simulation cell, even for the low TBA concentrations considered here. We note that these long-range correlations pose a serious problem if one wishes to obtain certain physical properties such as Kirkwood-Buff integrals from simulation results. In contrast, two other force fields that we consider show little sign of aggregation for Xt ≲ 0.08. In our 64 000 particle simulations all four models considered show demixing-like behavior for Xt ≳ 0.1, although such behavior is not evident in smaller systems of 2000 particles. The meaning of the demixing-like behavior is unclear. Since real TBA-water solutions do not demix, it might be an indication that all four models we consider poorly represent the real system. Alternatively, it might be an artifact of finite system size. Possibly, the apparent demixing indicates that for Xt ≳ 0.1, the stable TBA aggregates are simply too large to fit into the simulation cell. Our results provide a view of the

  16. Oxidative Mineralization and Characterization of Polyvinyl Alcohol Solutions for Wastewater Treatment

    SciTech Connect

    Oji, L.N.

    2003-08-07

    Photochemical and ultrasonic treatment of polyvinyl alcohol (PVA), derived from PVA fabric material, with hydrogen peroxide was evaluated as a primary method for PVA mineralization into simpler organic molecules. PVA-based waste streams have been found to be compatible with nuclear process wastewater treatment facilities only when solubilized PVA is more than 90 percent mineralized with hydrogen peroxide. No undesirable solid particles are formed with other nuclear process liquid waste when they are mixed, pH adjusted, evaporated and blended with this type of oxidized PVA waste streams. The presence of oxidized PVA in a typical nuclear process wastewater has been found to have no detrimental effect on the efficiency of ion exchange resins, inorganic, and precipitation agents used for the removal of radionuclides from nuclear waste streams. The disappearance of PVA solution in hydrogen peroxide with ultrasonic/ ultraviolet irradiation treatment was characterized by pseudo-first-order reaction kinetics. Radioactive waste contaminated PVA fabric can be solubilized and mineralized to produce processible liquid waste, hence, no bulky solid waste disposal cost can be incurred and the radionuclides can be effectively recovered. Therefore, PVA fabric materials can be considered as an effective substitute for cellulose fabrics that are currently used in radioactive waste decontamination processes.

  17. In vitro-in vivo sequence studies as a method of selecting the most efficacious alcohol-based solution for hygienic hand disinfection.

    PubMed

    Herruzo, R; Vizcaino, M J; Herruzo, I

    2010-05-01

    The use of alcohol-based hand rubs serves to reduce hospital-acquired infections. Many products of this type are now on offer and it is essential to know how to rank their efficacy. A sequence of tests is proposed here to compare any given new alcohol-based solution against the reference solution (60% 2-isopropyl-alcohol) with 30 s of contact time: (i) in vitro (with pig skin as carrier) testing of >30 species of microorganism; (ii) in vitro assessment of residual efficacy (after 30 min of drying); (iii) in vivo study of transient microbiota (modification of the EN 1500 standard procedure) using four ATCC strains; (iv) in vivo study of resident hand microbiota. After performing the in vitro evaluation of seven alcohol-based hand rubs, the two most efficacious (chlorhexidine-quac-alcohol and mecetronium- alcohol) were chosen and studied, comparatively with the reference solution (60% isopropyl alcohol), in vitro (for chemical sustainability on the skin) and in vivo (against transient and resident microbiota). Chlorhexidine-quac-alcohol proved to be significantly superior to mecetronium-alcohol or the reference solution in all tests, except against resident microbiota for which the improvement was not statistically significant. PMID:19624506

  18. Removal of Uranium From Aqueous Solution by Carbon Nanotubes.

    PubMed

    Yu, Jing; Wang, Jianlong

    2016-10-01

    The adsorption of uranium onto carbon nanotubes (CNTs) was investigated. The effect of solution pH, contact time, initial uranium concentration, and temperature on the adsorption capacity of uranium was determined. CNTs were characterized by using scanning electron microscopy (SEM), transmission electron microscopy (TEM), powder x-ray diffraction (XRD), Raman spectra, and the Fourier infrared spectra (FTIR). The diameters of the CNTs varied from 10 to 50 nm in diameter and 1 ~ 2 μm in length. FTIR spectra analysis indicated that carboxyl groups were involved in adsorption of U(VI) by CNTs. The experimental results showed that U(VI) adsorption onto CNTs reached equilibrium within 10 min, and the removal efficiency was 95% at pH = 5. The adsorption kinetics of U(VI) could be described by a pseudo first-order kinetic model. The adsorption isotherm conformed to the Slips model. The adsorption process was spontaneous and endothermic. PMID:27575349

  19. Spray-on polyvinyl alcohol separators and impact on power production in air-cathode microbial fuel cells with different solution conductivities.

    PubMed

    Hoskins, Daniel L; Zhang, Xiaoyuan; Hickner, Michael A; Logan, Bruce E

    2014-11-01

    Separators are used to protect cathodes from biofouling and to avoid electrode short-circuiting, but they can adversely affect microbial fuel cell (MFC) performance. A spray method was used to apply a polyvinyl alcohol (PVA) separator to the cathode. Power densities were unaffected by the PVA separator (339±29mW/m(2)), compared to a control lacking a separator in a low conductivity solution (1mS/cm) similar to wastewater. Power was reduced with separators in solutions typical of laboratory tests (7-13mS/cm), compared to separatorless controls. The PVA separator produced more power in a separator assembly (SEA) configuration (444±8mW/m(2)) in the 1mS/cm solution, but power was reduced if a PVA or wipe separator was used in higher conductivity solutions with either Pt or activated carbon catalysts. Spray and cast PVA separators performed similarly, but the spray method is preferred as it was easier to apply and use. PMID:25260178

  20. Adsorption of methylene blue and Congo red from aqueous solution by activated carbon and carbon nanotubes.

    PubMed

    Szlachta, M; Wójtowicz, P

    2013-01-01

    This study was conducted to determine the adsorption removal of dyes by powdered activated carbon (PAC, Norit) and multi-walled carbon nanotubes (MWCNTs, Chinese Academy of Science) from an aqueous solution. Methylene blue (MB) and Congo red (CR) were selected as model compounds. The adsorbents tested have a high surface area (PAC 835 m(2)/g, MWCNTs 358 m(2)/g) and a well-developed porous structure which enabled the effective treatment of dye-contaminated waters and wastewaters. To evaluate the capacity of PAC and MWCNTs to adsorb dyes, a series of batch adsorption experiments was performed. Both adsorbents exhibited a high adsorptive capacity for MB and CR, and equilibrium data fitted well with the Langmuir model, with the maximum adsorption capacity up to 400 mg/g for MB and 500 mg/g for CR. The separation factor, RL, revealed the favorable nature of the adsorption process under experimental conditions. The kinetics of adsorption was studied at various initial dye concentrations and solution temperatures. The pseudo-second-order model was used for determining the adsorption kinetics of MB and CR. The data obtained show that adsorption of both dyes was rapid in the initial stage and followed by slower processing to reach the plateau. The uptake of dyes increased with contact time, irrespective of their initial concentration and solution temperature. However, changes in the solution temperature did not significantly influence dye removal. PMID:24292474

  1. Ethylbenzene Removal by Carbon Nanotubes from Aqueous Solution

    PubMed Central

    Bina, Bijan; Pourzamani, Hamidreza; Rashidi, Alimorad; Amin, Mohammad Mehdi

    2012-01-01

    The removal of ethylbenzene (E) from aqueous solution by multiwalled, single-walled, and hybrid carbon nanotubes (MWCNTs, SWCNTs, and HCNTs) was evaluated for a nanomaterial dose of 1 g/L, concentration of 10–100 mg/L, and pH 7. The equilibrium amount removed by SWCNTs (E: 9.98 mg/g) was higher than by MWCNTs and HCNTs. Ethylbenzene has a higher adsorption tendency on CNTs, so that more than 98% of it adsorbed in first 14 min, which is related to the low water solubility and the high molecular weight. The SWCNTs performed better for ethylbenzene sorption than the HCNTs and MWCNTs. Isotherms study indicates that the BET isotherm expression provides the best fit for ethylbenzene sorption by SWCNTs. Carbon nanotubes, specially SWCNTs, are efficient and rapid adsorbents for ethylbenzene which possess good potential applications to maintain high-quality water. Therefore, it could be used for cleaning up environmental pollution to prevent ethylbenzene borne diseases. PMID:22187576

  2. Investigation of the properties of unidirectional fiber assemblies of single walled carbon nanotube-polyvinyl alcohol composite

    NASA Astrophysics Data System (ADS)

    Razal, Joselito M.

    Carbon nanotubes are difficult to process and this lack of convenient processibility has restricted their use for composite applications. High intensity sonication in surfactant solution has been the most common process used for nanotube exfoliation. Here we utilize our previously reported method to produce continuous SWNT composite fibers having mechanical properties that compare very favorably to recognized man-made or natural so-called "super" fibers such as Kevlar and spider silk. The process involved spinning an exfoliated dispersion of nanotubes into a bath of polyvinyl alcohol (PVA). We further improved our spinning method by using a spinning solution enriched with individual tubes we obtained by ultracentrifugation. The exfoliated state of SWNTs initially present in the spinning solution is preserved in our composite fiber assemblies as monitored using various spectroscopic and microscopic techniques. More importantly, these modifications allowed us to control the final composition and morphology of the assemblies so that the effects of relative concentration and degree of crystallinity on mechanical strength could be investigated. While the interaction between the SWNTs is strictly non-covalent, we find that increasing the accessible surface area of the nanotubes by de-bundling maximizes stress transfer to the polymer matrix, and thus dramatically enhances composite reinforcement. We also correlated the total nanotube surface area with the degree of crystalline domains together with the effects of post-treatment processing. Without employing any fiber treatment, we demonstrated that crystallinity linearly increased with effective nanotube surface area and showed slight improvements in mechanical properties. Moreover, after post-spinning treatments, crystallinity and tensile strength are further increased by factors of 21--40% and 232--437%,respectively. Mechanical drawing was the dominant factor in enhancement of mechanical properties, and is believed to

  3. Experimental Evidence of the Effect of Evaporation-Condensation on Thermal Marangoni Flows in Aqueous Fatty Alcohol Solutions.

    PubMed

    Azouni; Pétré

    1998-10-01

    The static surface tension (final sigmae) of aqueous solutions of a fatty alcohol versus temperature exhibits a minimum. Thus, a temperature gradient which is created at the free surface of such a solution at temperatures higher than that of the minimum (final sigmae) should induce a surface flow from the cold area to the hot one. This was indeed observed even at temperatures much lower than that of the minimum. A possible explanation is the evaporation of alcohol at the hot area where the surface tension increases, and its condensation on the cold area where the surface tension decreases, the alcohol being tranported by the gas phase. The thickness of the gas phase over the liquid could play a role in the observed flows. A device was built in which the thickness of the gas phase could be adjusted. Experiments performed with a 6.2 x 10(-3) m solution of n-heptanol indicate a lowering of the surface velocity where the thickness of the gas phase is reduced. Copyright 1998 Academic Press. PMID:9761660

  4. Impact of tert-butyl alcohol on crystallization kinetics of gemcitabine hydrochloride in frozen aqueous solutions.

    PubMed

    Munjal, Bhushan; Bansal, Arvind K

    2015-01-01

    The effect of tert-butyl alcohol (TBA) on isothermal crystallization kinetics of gemcitabine hydrochloride (GHCl) in frozen aqueous solutions was assessed by cold-stage microscopy. Addition of TBA (0%-5%, w/w) increased the value of Johnson-Mehl-Avrami rate constant (1.3-33.3 h⁻¹) and reduced the Avrami exponent (2.5-1.0). Thermodynamic parameters [enthalpy (ΔH(‡)), entropy (ΔS(‡)), and free energy (ΔG(‡)) of activation], calculated using Arrhenius and Eyring-Polanyi equations, established that TBA (2%, w/w) accelerated GHCl crystallization by reducing its ΔH(‡) (53.9 cf. 96.5 kJ/mol⁻¹) and ΔG(‡) (68.5 cf. 74.9 kJ/mol⁻¹). Further, to explore insights into the effect of TBA on nucleation and crystal growth of GHCl, crystallization kinetics data were deconvolved using Finke-Watzky model. This revealed that addition of TBA decreased ΔH(‡) of nucleation and increased ΔS(‡) of crystal growth, thereby reducing ΔG(‡) of nucleation and crystal growth by 11.7% and 4.2%, respectively. Finkey-Watzky model also predicted a reduction in the crystal size upon TBA addition, which was confirmed by comparing particle size of GHCl lyophilized in the presence and absence of TBA. In conclusion, TBA reduces ΔG(‡) of nucleation and crystal growth in a differential manner, thereby enhancing the crystallization kinetics of GHCl and affecting its morphological features. PMID:25393155

  5. Dual Catalysis Using Boronic Acid and Chiral Amine: Acyclic Quaternary Carbons via Enantioselective Alkylation of Branched Aldehydes with Allylic Alcohols.

    PubMed

    Mo, Xiaobin; Hall, Dennis G

    2016-08-31

    A ferrocenium boronic acid salt activates allylic alcohols to generate transient carbocations that react with in situ-generated chiral enamines from branched aldehydes. The optimized conditions afford the desired acyclic products embedding a methyl-aryl quaternary carbon center with up to 90% yield and 97:3 enantiomeric ratio, with only water as the byproduct. This noble-metal-free method complements alternative methods that are incompatible with carbon-halogen bonds and other sensitive functional groups. PMID:27518200

  6. A mesoporous carbon-supported Pt nanocatalyst for the conversion of lignocellulose to sugar alcohols.

    PubMed

    Park, Dae Sung; Yun, Danim; Kim, Tae Yong; Baek, Jayeon; Yun, Yang Sik; Yi, Jongheop

    2013-12-01

    The conversion of lignocellulose is a crucial topic in the renewable and sustainable chemical industry. However, cellulose from lignocellulose is not soluble in polar solvents, and is, therefore, difficult to convert into value-added chemicals. A strategy to overcome this drawback is the use of mesoporous carbon, which enhances the affinity between the cellulose and the catalyst through its abundant functional groups and large uniform pores. Herein, we report on the preparation of a Pt catalyst supported on a type of 3D mesoporous carbon inspired by Echinometra mathae (Pt/CNE) to enhance the interaction between the catalyst and a nonsoluble reactant. In the hydrolytic hydrogenation of cellulose, the abundant oxygen groups of CNE facilitated the access of cellulose to the surface of the catalyst, and the open pore structure permits cello-oligomers to effectively diffuse to the active sites inside the pore. The highly dispersed Pt performed dual roles: hydrolysis by in situ generating protons from H2 or water as well as effective hydrogenation. The use of the Pt/CNE catalyst resulted in an approximately 80 % yield of hexitol, the best performance reported to date. In direct conversion of hardwood powder, the Pt/CNE shows good performance in the production of sugar alcohols (23 % yield). We expect that the open-structured 3D carbon will be widely applied to the conversion of various lignocellulosic materials. PMID:24227502

  7. Solubility of plutonium(VI) carbonate in saline solutions

    NASA Astrophysics Data System (ADS)

    Reilly, Sean D.; Runde, Wolfgang; Neu, Mary P.

    2007-06-01

    Among the plutonium oxidation states found to form in the environment, mobile plutonium(VI) can exist under oxidizing conditions and in waters with high chloride content due to radiolysis effects. We are investigating the solubility and speciation of plutonium(VI) carbonate under conditions relevant to natural waters and brines such as those found near some geologic radioactive waste repositories. The solid Pu(VI) phase PuO 2CO 3(s) was prepared and its solubility was measured in NaCl and NaClO 4 solutions in a CO 2 atmosphere as a function of pH and ionic strength (0.1-5.6 m). The concentration of soluble plutonium in solution was calculated from spectroscopic data and liquid scintillation counting. Spectroscopic measurements also revealed the plutonium oxidation state. The apparent solubility product of PuO 2CO 3(s) was determined at selected electrolyte concentrations to be, log Ks,0 = -13.95 ± 0.07 (0.1 m NaCl), log Ks,0 = -14.07 ± 0.13 (5.6 m NaCl), and log Ks,0 = -15.26 ± 0.11 (5.6 m NaClO 4). Specific ion interaction theory was used to calculate the solubility product at zero ionic strength, logKs,0∘=-14.82±0.05.

  8. [Disinfection efficacy of hand hygiene based on chlorhexidine gluconate content and usage of alcohol-based hand-rubbing solution].

    PubMed

    Tanaka, Ippei; Watanabe, Kiyoshi; Nakaminami, Hidemasa; Azuma, Chihiro; Noguchi, Norihisa

    2014-01-01

    Recently, the procedure for surgical hand hygiene has been switching to a two-stage method and hand-rubbing method from the traditional hand-scrubbing method. Both the two-stage and hand-rubbing methods use alcohol-based hand-rubbing after hand washing. The former requires 5 min of antiseptic hand washing, and the latter 1 min of nonantiseptic hand washing. For a prolonged bactericidal effect in terms of surgical hand hygiene, chlorhexidine gluconate (CHG) has been noted due to its residual activity. However, no detailed study comparing the disinfection efficacy and prolonged effects according to different contents of CHG and the usage of alcohol-based hand-rubbing has been conducted. The glove juice method is able to evaluate disinfection efficacy and prolonged effects of the disinfectants more accurately because it can collect not only transitory bacteria but also normal inhabitants on hands. In the present study, we examined the disinfection efficacy and prolonged effects on alcohol-based hand-rubbing containing CHG by six hand-rubbing methods and three two-stage methods using the glove juice method. In both methods, 3 mL (one pump dispenser push volume) alcohol-based hand-rubbing solution containing 1% (w/v) CHG showed the highest disinfection efficacy and prolonged effects, and no significant difference was found between the hand-rubbing and two-stage methods. In the two methods of hand hygiene, the hand-rubbing method was able to save time and cost. Therefore, the data strongly suggest that the hand-rubbing method using a one pump dispenser push volume of alcohol-based hand-rubbing solution containing 1% (w/v) CHG is suitable for surgical hand hygiene. PMID:25366919

  9. Porous carbon materials synthesized using IRMOF-3 and furfuryl alcohol as precursor

    NASA Astrophysics Data System (ADS)

    Deka, Pemta Tia; Ediati, Ratna

    2016-03-01

    IRMOF-3 crystals have been synthesized using solvothermal method by adding zinc nitrate hexahydrate with 2-amino-1,4-benzenedicarboxylic acid in N'N-dimethylformamide (DMF) at 100°C for 24 (note as IR-24) and 72 h (note as IR-72). The obtained crystals were characterized using X-ray Diffraction (XRD), SEM (Scanning Electron Microscopy) and Scanning Electron Microscopy-Energy Dispersive X-ray (SEM-EDX), FTIR and Isothermal adsorption-desorption N2. The diffractogram solids synthesized show characteristic peak at 2θ 6.8, 9.6 and 13.7°. SEM micrograph show cubic shape of IRMOF-3 crystal. Based on FTIR characterization, IRMOF-3 appear at wavelength (1691,46; 1425,3; 1238,21; 1319,22 dan 3504,42)cm-1. The Isotherm of crystal IRMOF-3 at heating time 24 h and 72 h are type IV. The surface area of IR-24 and IR-72 are respectively 24,758 m2/g and 29,139 m2/g with its dominant mesopores. Carbonaceous materials has been successfully synthesized using IR-24, IR-72 and furfuryl alcohol (FA) as second carbon precursor with variation of carbonation temperature 550, 700 and 850°C. The XRD result from both carbonaceous materials show formation of amorphous carbon and caharacteristic peak of ZnO oxide. Micrograph SEM show that carbonaceous materials have cubic shape as IRMOF-3 and SEM-EDX result indicate Zn and nitrogen content of these materials has decrease until temperature 850°C. Porous carbon using IR-24 and FA (notes as C-24) has increased surface area with higher carbonation temperature. The highest surface area is 1495,023 m2/g. Total pore volume and pore size of C-24 from low to high temperature respectively as (0,338; 0,539 and 1,598) cc/g; (0,107; 0,152 and 0,610) cc/g. Porous carbon using IR-72 and FA (notes as C-72) has smaller surface area than C-24 but its also increased during higher carbonation heating. The highest surface area is 1029,668 m2/g.The total pore volume and pore size of these carbon materials from low to high temperature respectively as (0,390; 0

  10. Behavior of Ni2+ cations in aqueous and alcohol solutions of NiCl2 · 6H2O

    NASA Astrophysics Data System (ADS)

    Petkova, P.; Nedkov, V.; Vasilev, P.; Ismailov, I.

    2014-09-01

    We have investigated the optical properties of Ni2+ cations in aqueous and alcohol solutions of NiCl2 · 6H2O at room temperature. We measured the absorption spectra of these two types of solutions in the spectral region 395-795 nm. The Racah’s parameters and the exchange integrals of the aqueous complex [Ni(H2O)6]2+ have been calculated. The parameters Dq, Dt and Ds are also calculated on the basis of our experimental data. The parameters δσ and δπ, connected with the symmetry of the complex, are determined.

  11. Stable TEMPO and ABNO Catalyst Solutions for User-Friendly (bpy)Cu/Nitroxyl-Catalyzed Aerobic Alcohol Oxidation.

    PubMed

    Steves, Janelle E; Stahl, Shannon S

    2015-11-01

    Two solutions, one consisting of bpy/TEMPO/NMI and the other bpy/ABNO/NMI (bpy =2,2'-bipyridyl; TEMPO = 2,2,6,6-tetramethylpiperidine N-oxyl, ABNO = 9-azabicyclo[3.3.1]nonane N-oxyl; NMI = N-methylimidazole), in acetonitrile are shown to have good long-term stability (≥1 year) under air at 5 °C. The solutions may be combined in appropriate quantities with commercially available [Cu(MeCN)4]OTf to provide a convenient catalyst system for the aerobic oxidation of primary and secondary alcohols. PMID:26457658

  12. Effect of chronic carbon monoxide exposure on experimental alcoholic liver injury in rats

    SciTech Connect

    Nanji, A.A. ); Jui, L.T.; French, S.W. )

    1989-01-01

    Two groups of experimental animals with pair-fed controls were studied to evaluate the effect of chronic carbon monoxide (CO) exposure on progression of experimental alcoholic liver injury. Eight pairs of male Wistar rats were continuously infused liquid diet and ethanol or isocaloric dextrose for four months. Four pairs were also exposed to CO. Liver damage was followed monthly by serum ALT and morphologic assessment of liver biopsy. Serum levels of ALT were significantly higher in the CO-ethanol group compared to other groups. Electron microscopy revealed a greater degree of cell necrosis in the CO exposed group which explained the significantly higher ALT activity in these animals. Both experimental groups had significantly greater liver damage than controls. Carboxyhemoglobin levels were not different in the ethanol-fed and control group. Our results show that chronic CO exposure enhances liver cell necrosis in ethanol-fed rats thereby lending support to the hypothesis that ethanol and hypoxia enhance cellular disruption in the liver which could be important in the pathogenesis of alcoholic liver disease in rats.

  13. Effect of Acid and Alcohol Network Forces within Functionalized Multiwall Carbon Nanotubes Bundles on Adsorption of Copper (II) Species

    EPA Science Inventory

    Adsorption of metals on carbon nanotubes (CNTs) has important applications in sensors, membranes, and water treatment. The adsorptive capacity of multiwall CNTs for copper species in water depends on the type of functional group present on their surface. The alcohol (COOH) and ac...

  14. Structural and phase transition changes of sodium dodecyl sulfate micellar solution in alcohols probed by small-angle neutron scattering (SANS)

    SciTech Connect

    Putra, Edy Giri Rachman; Patriati, Arum

    2015-04-16

    Small-angle neutron scattering (SANS) measurements on 0.3M sodium dodecyl sulfate (SDS) micellar solutions have been performed in the presence of n-alcohols, from ethanol to decanol at different alcohol concentrations, 2–10 wt%. The ellipsoid micellar structure which occurred in the 0.3M SDS in aqueous solution with the size range of 30–50 Å has different behavior at various hydrocarbon chain length and concentration of alcohols. At low concentration and short chain-length of alcohols, such as ethanol, propanol, and butanol, the size of micelles reduced and had a spherical-like structure. The opposite effect occurred as medium to long chain alcohols, such as hexanol, octanol and decanol was added into the 0.3M SDS micellar solutions. The micelles structure changed to be more elongated in major axis and then crossed the critical phase transition from micellar solution into liquid crystal phase as lamellar structure emerged by further addition of alcohols. The inter-lamellar distances were also depending on the hydrocarbon chain length and concentration of alcohols. In the meantime, the persistent micellar structures occurred in addition of medium chain of n-alcohol, pentanol at all concentrations.

  15. Preparation of novel carbon microfiber/carbon nanofiber-dispersed polyvinyl alcohol-based nanocomposite material for lithium-ion electrolyte battery separator.

    PubMed

    Sharma, Ajit K; Khare, Prateek; Singh, Jayant K; Verma, Nishith

    2013-04-01

    A novel nanocomposite polyvinyl alcohol precursor-based material dispersed with the web of carbon microfibers and carbon nanofibers is developed as lithium (Li)-ion electrolyte battery separator. The primary synthesis steps of the separator material consist of esterification of polyvinyl acetate to produce polyvinyl alcohol gel, ball-milling of the surfactant dispersed carbon micro-nanofibers, mixing of the milled micron size (~500 nm) fibers to the reactant mixture at the incipience of the polyvinyl alcohol gel formation, and the mixing of hydrophobic reagents along with polyethylene glycol as a plasticizer, to produce a thin film of ~25 μm. The produced film, uniformly dispersed with carbon micro-nanofibers, has dramatically improved performance as a battery separator, with the ion conductivity of the electrolytes (LiPF6) saturated film measured as 0.119 S-cm(-1), approximately two orders of magnitude higher than that of polyvinyl alcohol. The other primary characteristics of the produced film, such as tensile strength, contact angle, and thermal stability, are also found to be superior to the materials made of other precursors, including polypropylene and polyethylene, discussed in the literature. The method of producing the films in this study is novel, simple, environmentally benign, and economically viable. PMID:23827627

  16. Fabrication of porous chitosan/poly(vinyl alcohol) reinforced single-walled carbon nanotube nanocomposites for neural tissue engineering.

    PubMed

    Shokrgozar, Mohammad Ali; Mottaghitalab, Fatemeh; Mottaghitalab, Vahid; Farokhi, Mehdi

    2011-04-01

    With the ability to form a nano-sized fibrous structure with large pore sizes mimicking the extracellular matrix (ECM), electrospinning was used to fabricate chitosan/poly(vinyl alcohol) nanofibers reinforced by single-walled carbon nanotube (SWNT-CS/PVA) for potential use in neural tissue engineering. Moreover, ultrasonication was performed to fabricate highly dispersed SWNT/CS solution with 7%, 12%, and 17% SWNT content prior to electrospinning process. In the present study, a number of properties of CS/PVA reinforced SWNTs nanocomposites were evaluated. The in vitro biocompatibility of the electrospun fiber mats was also assessed using human brain-derived cells and U373 cell lines. The results have shown that SWNTs as reinforcing phase can augment the morphology, porosity, and structural properties of CS/PVA nanofiber composites and thus benefit the proliferation rate of both cell types. In addition, the cells exhibit their normal morphology while integrating with surrounding fibers. The results confirmed the potential of SWNT-CS/PVA nanocomposites as scaffold for neural tissue engineering. PMID:21702365

  17. Alkaline direct ethanol fuel cell performance using alkali-impregnated polyvinyl alcohol/functionalized carbon nano-tube solid electrolytes

    NASA Astrophysics Data System (ADS)

    Huang, Chien-Yi; Lin, Jia-Shiun; Pan, Wen-Han; Shih, Chao-Ming; Liu, Ying-Ling; Lue, Shingjiang Jessie

    2016-01-01

    This study investigates the application of a polyvinyl alcohol (PVA)/functionalized carbon nano-tubes (m-CNTs) composite in alkaline direct ethanol fuel cells (ADEFC). The m-CNTs are functionalized with PVA using the ozone mediation method, and the PVA composite containing the modified CNTs is prepared. Adding m-CNT into the PVA matrix enhances the alkaline uptake and the ionic conductivity of the KOH-doped electrolyte. Meanwhile, the m-CNT-containing membrane exhibited a lower swelling ratio and suppressed ethanol permeability compared to the pristine PVA film. The optimal condition for the ADEFC is determined to be under operation at an anode feed of 3 M ethanol in a 5 M KOH solution (at a flow rate of 5 cm3 min-1) with a cathode feed of moisturized oxygen (with a flow rate of 100 cm3 min-1) and the KOH-doped PVA/m-CNT electrolyte. We achieved a peak power density value of 65 mW cm-2 at 60 °C, which is the highest among the ADEFC literature data and several times higher than the proton-exchange direct ethanol fuel cells using sulfonated membrane electrolytes. Therefore, the KOH-doped PVA/m-CNT electrolyte is a suitable solid electrolyte for ADEFCs and has potential for commercialization in alkaline fuel cell applications.

  18. Carbon Footprint of Telemedicine Solutions - Unexplored Opportunity for Reducing Carbon Emissions in the Health Sector

    PubMed Central

    Holmner, Åsa; Ebi, Kristie L.; Lazuardi, Lutfan; Nilsson, Maria

    2014-01-01

    Background The healthcare sector is a significant contributor to global carbon emissions, in part due to extensive travelling by patients and health workers. Objectives To evaluate the potential of telemedicine services based on videoconferencing technology to reduce travelling and thus carbon emissions in the healthcare sector. Methods A life cycle inventory was performed to evaluate the carbon reduction potential of telemedicine activities beyond a reduction in travel related emissions. The study included two rehabilitation units at Umeå University Hospital in Sweden. Carbon emissions generated during telemedicine appointments were compared with care-as-usual scenarios. Upper and lower bound emissions scenarios were created based on different teleconferencing solutions and thresholds for when telemedicine becomes favorable were estimated. Sensitivity analyses were performed to pinpoint the most important contributors to emissions for different set-ups and use cases. Results Replacing physical visits with telemedicine appointments resulted in a significant 40–70 times decrease in carbon emissions. Factors such as meeting duration, bandwidth and use rates influence emissions to various extents. According to the lower bound scenario, telemedicine becomes a greener choice at a distance of a few kilometers when the alternative is transport by car. Conclusions Telemedicine is a potent carbon reduction strategy in the health sector. But to contribute significantly to climate change mitigation, a paradigm shift might be required where telemedicine is regarded as an essential component of ordinary health care activities and not only considered to be a service to the few who lack access to care due to geography, isolation or other constraints. PMID:25188322

  19. Experimental fractionation of stable carbon isotopes during degassing of carbon dioxide and precipitation of calcite from aqueous solutions

    NASA Astrophysics Data System (ADS)

    Müller, K.; Winde, V.; Escher, P.; von Geldern, R.; Böttcher, M. E.

    2012-04-01

    Processes in the carbonate system of surface waters are in particular sensitive to variations of boundary conditions as, for instance, the partial pressure of carbon dioxide in the atmosphere and the aqueous solution. Examples range from streams, rivers, to coastal marine waters. The flux of carbon dioxide from continental flowing waters was recently included into calculations of the global carbon budget (Butman & Raymond, 2011, Nature Geo.). These solutions, are often supersaturated in carbon dioxide with respect to the atmosphere. The degassing of carbon dioxide is associated with a kinetically controlled fractionation of the stable carbon isotopes, which has to be considered in balancing water-air carbon dioxide fluxes. The degassing process additionally leads to the super-saturation of the aqueous solution with respect to calcium carbonate. Stable isotope fractionation is of particular value to identify and quantify processes at the water-gas phase interface and link these non-equilibrium processes to the formation mechanisms of calcite and the hydrodynamics of surface waters. Experiments were carried out with or without inert N2 gas flow to degas carbon dioxide from initially supersaturated solutions. Natural solutions used are from different stations of the Elbe estuary, the Jade Bay, the backbarrier tidal area of Spiekeroog Island, carbonate springs of Rügen Island, and the Baltic Sea coastline. Results are compared experiments using bottled mineral waters. By following the (physico) chemical changes in the solutions (pH, TA, Ca PHREEQC modeling) it was found, that two evolutionary stages can be differentiated. Reaction progress led to the preferential liberation of carbon dioxide containing the light carbon isotope, following a Rayleigh-type process. After an induction period, where only degassing of carbon dioxide took place, a second stage was observed where calcite began to form from the highly supersaturated solutions. In this stage the carbonate

  20. Effect of a magnetic field on the dissolution kinetics of carbon dioxide in aqueous solutions

    SciTech Connect

    Kruglitskii, N.N.; Kolomiets, A.A.; Kul'skii, L.A.; Rubezhanskii, K.A.; Zhantalai, B.P.

    1986-02-01

    This paper gives an account of an investigation into the effect of a magnetic field on the rate of dissolution of carbon dioxide in aqueous solutions. The CO/sub 2/ pressure in the system was maintained by a Hoffer valve. The method used for studying the dissolution kinetics of carbon dioxide in aqueous solutions is described. The specific rate of dissolution of carbon dioxide in solutions exposed to a magnetic field is lower than in solutions not so exposed. There is a tendency for the equilibrium solubility of CO/sub 2/ to increase in solutions exposed to a magnetic field.

  1. Leaching kinetics of malachite in ammonium carbonate solutions

    NASA Astrophysics Data System (ADS)

    Oudenne, Paul D.; Olson, Ferron A.

    1983-03-01

    Leaching of malachite was conducted with ammonium carbonate as lixiviant and with temperature, lixiviant concentration, and particle size as variables. Two stages of reaction were found. In Stage I, the initial dissolution of malachite proceeds rapidly, but after about 10 pct reaction the rate is reduced by surface blockage due to the presence of a needle-structured intermediate, presumably Cu(OH)2. Subsequently, malachite and the intermediate dissolve concurrently. In Stage II, after 90 pct reaction, essentially all of the malachite has dissolved and only the intermediate remains. It dissolves in Stage II. The activation energy is 64 kJ/mole (15.3 kcal/mole) for Stage I and 75 kJ/mole (18 kcal/mole) for Stage II. The rate of reaction in Stage I is proportional to the reciprocal of particle size and is 0.8 order with respect to the concentration of ammonium carbonate. The structures of leaching residues were studied using a scanning electron microscope. The kinetic data (activation energy and entropy), particle size and concentration dependence, residue morphology, and general leaching behavior evident from microscopic monitoring during leaching were used to develop the geometric equation for leaching in Stage I. The equation, based on a heterogeneous reaction with geometric rate control, is: 1 - (1 - α 1/3 = K01/r0/[(NH4)2C03]0.8 exp(-64,000/RT)t. It was deduced that initial steps in reaction were: (1) release of Cu2+ from malachite; (2) initial complexing with ammonia to form Cu(NH3)2+; and (3) subsequent complexing to produce Cu(NH3){4/2+} which is stable in solution at pH 8.8, the buffered pH of reaction. Stage II appears to be a similar reaction except that the reaction obeys cylindrical geometry instead of spherical geometry as in Stage I.

  2. Comparison of Chain Conformation of Poly(vinyl alcohol) in Solutions and Melts from Quantum Chemistry Based Molecular Dynamics Simulations

    NASA Technical Reports Server (NTRS)

    Jaffe, Richard; Han, Jie; Matsuda, Tsunetoshi; Yoon, Do; Langhoff, Stephen R. (Technical Monitor)

    1997-01-01

    Confirmations of 2,4-dihydroxypentane (DHP), a model molecule for poly(vinyl alcohol), have been studied by quantum chemistry (QC) calculations and molecular dynamics (MD) simulations. QC calculations at the 6-311G MP2 level show the meso tt conformer to be lowest in energy followed by the racemic tg, due to intramolecular hydrogen bond between the hydroxy groups. The Dreiding force field has been modified to reproduce the QC conformer energies for DHP. MD simulations using this force field have been carried out for DHP molecules in the gas phase, melt, and CHCl3 and water solutions. Extensive intramolecular hydrogen bonding is observed for the gas phase and CHCl3 solution, but not for the melt or aqueous solution, Such a condensed phase effect due to intermolecular interactions results in a drastic change in chain conformations, in agreement with experiments.

  3. The effect of poly(vinyl alcohol) on the photophysical properties of pyronin dyes in aqueous solution: A spectroscopic study

    NASA Astrophysics Data System (ADS)

    Gür, Bahri; Meral, Kadem

    2013-01-01

    The photophysical properties of pyronin B (PyB) and pyronin Y (PyY) in water and poly(vinyl alcohol) (PVA) aqueous solutions were studied by using absorption, steady-state fluorescence and time-resolved fluorescence spectroscopy techniques at room temperature. The spectroscopic and photophysical properties of pyronin dyes in the concentrated PVA aqueous solution were different than those found in water. The aggregation of the pyronin dyes in the concentrated PVA aqueous solution was prevented with ease while the dye aggregation was generally formed in water with high dye concentration. The decrease in the aggregation tendency of pyronin dyes in the concentrated PVA aqueous solution caused an increase in radiative transitions. The addition of PVA into the aqueous solution induced the enhancement in the fluorescence intensity of the dyes compared to those in water. As a result, the quantum yields of the dyes were improved by the addition of PVA at high loading. The time-resolved fluorescence study revealed that the fluorescence decay of dyes in all solutions were found to be single-exponential and the fluorescence lifetime of pyronin dyes in the concentrated PVA aqueous solution were also higher than those found in water.

  4. Polyvinyl alcohol gelation: A structural locking-up agent and carbon source for Si/CNT/C composites as high energy lithium ion battery anode

    NASA Astrophysics Data System (ADS)

    Chen, Dingqiong; Liao, Wenjuan; Yang, Yang; Zhao, Jinbao

    2016-05-01

    A novel polyvinyl alcohol (PVA) hydrogel method is developed to synthesize Si/CNT/C composites. The Si nanoparticles and CNTs are 'position' locked up by PVA hydrogel in a simple aqueous solution process, and then the Si-CNT-PVA hydrogel has pyrolyzed to form Si/CNT/C composites. In this unique structured Si/CNT/C composites, the CNTs form a porous network acting both as conductive agent for electron transfer and buffer space to accommodate huge Si volume change during lithiation/delithiation process, while the coating layer of carbon carbonized from polyvinyl alcohol (PVA) hydrogel is conducive to stabilize the interweaved composite structure. The complex structures of Si/CNT/C composites and their electrochemical properties are presented in this paper. The Si/CNT/C composites exhibit an initial reversible capacity of nearly 800 mAhg-1, an excellent capacity retention of 97.1% after 100 cycles at the rate of 0.1 C, and high capacity retention even at high current rate.

  5. Polyvinyl alcohol gelation: A structural locking-up agent and carbon source for Si/CNT/C composites as high energy lithium ion battery anode

    NASA Astrophysics Data System (ADS)

    Chen, Dingqiong; Liao, Wenjuan; Yang, Yang; Zhao, Jinbao

    2016-05-01

    A novel polyvinyl alcohol (PVA) hydrogel method is developed to synthesize Si/CNT/C composites. The Si nanoparticles and CNTs are 'position' locked up by PVA hydrogel in a simple aqueous solution process, and then the Si-CNT-PVA hydrogel has pyrolyzed to form Si/CNT/C composites. In this unique structured Si/CNT/C composites, the CNTs form a porous network acting both as conductive agent for electron transfer and buffer space to accommodate huge Si volume change during lithiation/delithiation process, while the coating layer of carbon carbonized from polyvinyl alcohol (PVA) hydrogel is conducive to stabilize the interweaved composite structure. The complex structures of Si/CNT/C composites and their electrochemical properties are presented in this paper. The Si/CNT/C composites exhibit an initial reversible capacity of nearly 800 mAhg-1, an excellent capacity retention of 97.1% after 100 cycles at the rate of 0.1 C, and high capacity retention even at high current rate.

  6. Benzyl alcohol oxidation in supercritical carbon dioxide: spectroscopic insight into phase behaviour and reaction mechanism.

    PubMed

    Caravati, Matteo; Grunwaldt, Jan-Dierk; Baiker, Alfons

    2005-01-21

    Selective oxidation of benzyl alcohol to benzaldehyde with molecular oxygen over an alumina-supported palladium catalyst was performed with high rate at about 95% selectivity in supercritical carbon dioxide. The experiments in a continuous flow fixed-bed reactor showed that the pressure has a strong influence on the reaction rate. A marked increase of the rate (turnover frequency) from 900 h(-1) to 1800 h(-1) was observed when increasing the pressure from 140 to 150 bar. Video monitoring of the bulk fluid phase behavior and the simultaneous investigation by transmission and attenuated total reflection (ATR) infrared spectroscopy at two positions of the view cell showed that the sharp increase in activity is correlated to a transition from a biphasic to a monophasic reaction mixture. In the single phase region, both oxygen and benzyl alcohol are dissolved in the supercritical CO2 phase, which leads to a reduction of the mass transport resistances (both in the external fluid film and in the catalyst pores) and thus to the high reaction rate measured in the catalytic experiments. The phase transition could be effectively and easily monitored by transmission and ATR-IR spectroscopy despite the small concentration of the dense liquid like phase. Deposition of the Pd/Al2O3 catalyst on the ATR-crystal at the bottom of the view cell allowed to gain insight into the chemical changes and mass transfer processes occurring in the solid/liquid interface region during reaction. Analyzing the shift of the upsilon2 bending mode of CO2 gave information on the fluid composition in and outside the catalyst pores. Moreover, the catalytic reaction could be investigated in situ in this spectroscopic batch reactor cell by monitoring simultaneously the reaction progress, the phase behaviour and the catalytic interface. PMID:19785149

  7. Solubility of carbon dioxide in aqueous solutions of 2-amino-2-methyl-1,3-propanediol

    SciTech Connect

    Baek, J.I.; Yoon, J.H.

    1998-07-01

    The equilibrium solubility of carbon dioxide in aqueous solutions of 2-amino-2-methyl-1,3-propanediol (AMPD) has been measured at (30, 40, and 60) C and the partial pressure of carbon dioxide ranging from (0.5 to 3065) kPa. The concentrations of the aqueous solutions were (10 and 30) mass % AMPD. The tendency of the solubility of carbon dioxide in 30 mass % AMPD aqueous solution at 40 C was found to be similar to that in 30 mass % N-methyldiethanolamine aqueous solution.

  8. On the black carbon problem and its solutions

    NASA Astrophysics Data System (ADS)

    Jacobson, M. Z.

    2010-12-01

    Black carbon (BC) warms air temperatures in at least seven major ways: (a) directly absorbing downward solar radiation, (b) absorbing upward reflected solar radiation when it is situated above bright surfaces, such as snow, sea ice, and clouds, (c) absorbing some infrared radiation, (d) absorbing additional solar and infrared radiation upon obtaining a coating, (e) absorbing radiation multiply reflected within clouds when situated interstitially between cloud drops, (f) absorbing additional radiation when serving as CCN or scavenged inclusions within cloud drops, and (g) absorbing solar radiation when deposited on snow and sea ice, reducing the albedos of both. Modeling of the climate effects of BC requires treatment of all these processes in detail. In particular, treatment of BC absorption interstitially between cloud drops and from multiply-dispersed cloud drop BC inclusions must be treated simultaneously with treatment of cloud indirect effects to determine the net effects of BC on cloud properties. Here, results from several simulations of the effects of BC from fossil fuel and biofuel sources on global and regional climate and air pollution health are summarized. The simulations account for all the processes mentioned. Results are found to be statistically significant relative to chaotic variability in the climate system. Over time and in steady state, fossil-fuel soot plus biofuel soot are found to enhance warming more than methane. The sum of the soots causes less steady-state warming but more short term warming than does carbon dioxide. Thus eliminating soot emissions from both sources may be the fastest method of reducing rapid climate warming and possibly the only method of saving the Arctic ice. Eliminating such emissions may also reduce over 1.5 million deaths worldwide, particularly in developing countries. Short term mitigation options include the targeting of fossil-fuel and biofuel BC sources with particle traps, new stove technologies, and rural

  9. [Alcohol and drugs in Central Europe--problems and possible solutions].

    PubMed

    Nespor, K; Cs emy, L

    1994-08-22

    The high alcohol consumption and increasing abuse of other addictive inducing substances in Central Europe calls for broadley conceived preventive programmes and cheap and widely applicable therapeutic strategies (early treatment at the first contact level, self-help manuals, self-aid organizations). Social instability along with greater availability of alcohol and drugs create a dangerous combination. In addition to strategies of stress prevention at the societal level also strategy at the individual level is important (e.g. relaxation training, yoga, psychotherapy). It is also important to change the "image" of western society and commercial interests of those who make profits on alcohol and drugs should be under control and advertising should be greatly restricted if not prohibited. Prevention of problems caused by alcohol and drugs in particular in youths must be combined and really effective strategies should be used such as peer programmes. The authors mention also their own preventive programme FIT IN and print materials oriented specifically on certain population groups. PMID:7923324

  10. Oxidative Mineralization and Characterization of Polyvinyl Alcohol Solutions for Wastewater Treatment

    SciTech Connect

    Oji, L.N.

    1999-08-31

    The principal objectives of this study are to identify an appropriate polyvinyl alcohol (PVA) oxidative mineralization technique, perform compatibility and evaporation fate tests for neat and mineralized PVA, and determine potential for PVA chemical interferences which may affect ion exchange utilization for radioactive wastewater processing in the nuclear industry.

  11. Fetal Alcohol Syndrome: Understanding the Problem; Understanding the Solution; What Indian Communities Can Do.

    ERIC Educational Resources Information Center

    Streissguth, Ann P.

    1994-01-01

    Summarizes facts about fetal alcohol syndrome (FAS), including physical and mental symptoms; cause; prevalence overall and in Indian communities; and problems of infants, children, and adults with FAS. Emphasizes the importance of public awareness, professional education, and provision of community services to prevent FAS. Outlines specific…

  12. Solvent-free aerobic oxidation of hydrocarbons and alcohols with Pd@N-doped carbon from glucose.

    PubMed

    Zhang, Pengfei; Gong, Yutong; Li, Haoran; Chen, Zhirong; Wang, Yong

    2013-01-01

    The development of efficient systems for selective aerobic oxidation of hydrocarbons and alcohols to produce more functional compounds (aldehydes, ketones, acids or esters) with atmospheric air or molecular oxygen is a grand challenge for the chemical industry. Here we report the synthesis of palladium nanoparticles supported on novel nanoporous nitrogen-doped carbon, and their impressive performance in the controlled oxidation of hydrocarbons and alcohols with air. In terms of catalytic activity, these catalysts afford much higher turnover frequencies (up to 863 turnovers per hour for hydrocarbon oxidation and up to ~210,000 turnovers per hour for alcohol oxidation) than most reported palladium catalysts under the same reaction conditions. This work provides great potential for the application of ambient air and recyclable palladium catalysts in fine-chemical production with high activity. PMID:23481401

  13. CO2 adsorption properties of char produced from brown coal impregnated with alcohol amine solutions.

    PubMed

    Baran, Paweł; Zarębska, Katarzyna; Czuma, Natalia

    2016-07-01

    Carbon dioxide (CO2) emission reduction is critical to mitigating climate change. Power plants for heating and industry are significant sources of CO2 emissions. There is a need for identifying and developing new, efficient methods to reduce CO2 emissions. One of the methods used is flue gas purification by CO2 capture through adsorption. This study aimed to develop CO2 adsorbent out of modified brown coal impregnated with solutions of first-, second-, and third-order amines. Low-temperature nitrogen adsorption isotherms and CO2 isotherms were measured for the prepared samples. The results of experiments unexpectedly revealed that CO2 sorption capacity decreased after impregnation. Due to lack of strait trends in CO2 sorption capacity decrease, the results were closely analyzed to find the reason for the inconsistencies. It was revealed that different amines represent different affinities for CO2 and that the size and structure of impregnating factor has influence on the CO2 sorption capacity of impregnated material. The character of a support was also noticeable as well for impregnation results as for the affinity to CO2. The influence of amine concentration used was investigated along with the comparison on how the theoretical percentage of the impregnation on the support influenced the results. The reaction mechanism of tertiary amine was taken into consideration in connection to no presence of water vapor during the experiments. Key findings were described in the work and provide a strong basis for further studies on CO2 adsorption on amine-impregnated support. PMID:27317051

  14. Relation Between the Adsorbed Quantity and the Immersion Enthalpy in Catechol Aqueous Solutions on Activated Carbons

    PubMed Central

    Moreno-Piraján, Juan Carlos; Blanco, Diego; Giraldo, Liliana

    2012-01-01

    An activated carbon, CarbochemTM—PS230, was modified by chemical and thermal treatment in flow of H2, in order to evaluate the influence of the activated carbon chemical characteristics in the adsorption of the catechol. The catechol adsorption in aqueous solution was studied along with the effect of the pH solution in the adsorption process of modified activated carbons and the variation of immersion enthalpy of activated carbons in the aqueous solutions of catechol. The interaction solid-solution is characterized by adsorption isotherms analysis, at 298 K and pH 7, 9 and 11 in order to evaluate the adsorption value above and below that of the catechol pKa. The adsorption capacity of carbons increases when the solution pH decreases. The retained amount increases slightly in the reduced carbon to maximum adsorption pH and diminishes in the oxidized carbon. Similar conclusions are obtained from the immersion enthalpies, whose values increase with the solute quantity retained. In granular activated carbon (CAG), the immersion enthalpies obtained are between 21.5 and 45.7 J·g−1 for catechol aqueous solutions in a range of 20 at 1500 mg·L−1. PMID:22312237

  15. Kinetics of pyrite oxidation in sodium carbonate solutions

    SciTech Connect

    Ciminelli, V.S.T.; Osseo-Asare, K.

    1995-04-01

    The kinetics of pyrite oxidation in sodium carbonate solutions were investigated in a stirred vessel, under temperatures ranging from 50 C to 85 C, oxygen partial pressures from 0 to 1 atm, particle size fractions from {minus}150 + 106 to {minus}38 + 10 {mu}m ({minus}100 + 150 Mesh to {minus}400 Mesh + 10 {mu}m) and pH values of up to 12.5. The rate of the oxidation reaction is described by the following expression: {minus}dN/dt = SbkpO{sup 0.5}{sub 2} [OH{sup {minus}}]{sup 0.1} where N represents moles of pyrite, S is the surface area of the solid particles, b is a stoichiometric factor, k is an apparent rate constant, pO{sub 2} is the oxygen partial pressure, and [OH{sup {minus}}] is the hydroxyl ion concentration. The experimental data were fitted by a stochastic model for chemically controlled reactions, represented by the following fractional conversion (X) vs time (t) equation: (1 {minus} X){sup {minus}2/3} {minus} 1 = k{sub ST}t. The assumption behind this model, i.e., surface heterogeneity leading to preferential dissolution, is supported by the micrographs of reacted pyrite particles, showing pits created by localized dissolution beneath an oxide layer. In addition to the surface texture, the magnitude of the activation energy (60.0 kJ/mol or 14.6 {+-} 2.7 kcal/mol), the independence of rate on the stirring speed, the inverse relationship between the rate constant and the initial particle diameter, and the fractional reaction orders are also in agreement with a mechanism controlled by chemical reaction.

  16. Kinetics of pyrite oxidation in sodium carbonate solutions

    NASA Astrophysics Data System (ADS)

    Ciminelli, V. S. T.; Osseo-Asare, K.

    1995-04-01

    The kinetics of pyrite oxidation in sodium carbonate solutions were investigated in a stirred vessel, under temperatures ranging from 50 °C to 85 °C, oxygen partial pressures from 0 to 1 atm, particle size fractions from -150 + 106 to -38 + 10 µm (-100 + 150 Mesh to -400 Mesh + 10 µm) and pH values of up to 12.5. The rate of the oxidation reaction is described by the following expression: -dN/dt = SbkpO{2/0.5} [OH-]0.1 where N represents moles of pyrite, S is the surface area of the solid particles, b is a stoichiometric factor, k is an apparent rate constant, pO```2`` is the oxygen partial pressure, and [OH-] is the hydroxyl ion concentration. The experimental data were fitted by a stochastic model for chemically controlled reactions, represented by the following fractional conversion (X) vs time ( t) equation: (1-X)-2/3-1 = k STt The assumption behind this model, i.e., surface heterogeneity leading to preferential dissolution, is supported by the micrographs of reacted pyrite particles, showing pits created by localized dissolution beneath an oxide layer. In addition to the surface texture, the magnitude of the activation energy (60.9 kJ/mol or 14.6 ± 2.7 kcal/mol), the independence of rate on the stirring speed, the inverse relationship between the rate constant and the initial particle diameter, and the fractional reaction orders are also in agreement with a mechanism controlled by chemical reaction.

  17. Hydrothermal Carbonization: a feasible solution to convert biomass to soil?

    NASA Astrophysics Data System (ADS)

    Tesch, Walter; Tesch, Petra; Pfeifer, Christoph

    2013-04-01

    The erosion of fertile soil is a severe problem arising right after peak oil (Myers 1996). That this issue is not only a problem of arid countries is shown by the fact that even the European Commission defined certain milestones to address the problem of soil erosion in Europe (European Commission 2011). The application of bio-char produced by torrefaction or pyrolysis for the remediation, revegetation and restoration of depleted soils started to gain momentum recently (Rillig 2010, Lehmann 2011, Beesley 2011). Hydrothermal carbonization (HTC) is a promising thermo-chemical process that can be applied to convert organic feedstock into fertile soil and water, two resources which are of high value in regions being vulnerable to erosion. The great advantage of HTC is that organic feedstock (e.g. organic waste) can be used without any special pretreatment (e.g. drying) and so far no restrictions have been found regarding the composition of the organic matter. By applying HTC the organic material is processed along a defined pathway in the Van Krevelen plot (Behrendt 2006). By stopping the process at an early stage a nutritious rich material can be obtained, which is known to be similar to terra preta. Considering that HTC-coal is rich in functional groups and can be derived from the process under "wet" conditions, it can be expected that it shall allow soil bacteria to settle more easily compared to the bio-char derived by torrefaction or pyrolysis. In addition, up to 10 tons process water per ton organic waste can be gained (Vorlop 2009). Thus, as organic waste, loss of fertile soil and water scarcity becomes a serious issue within the European Union, hydrothermal carbonization can provide a feasible solution to address these issues of our near future. The presentation reviews the different types of feedstock investigated for the HTC-Process so far and gives an overview on the current stage of development of this technology. References Beesley L., Moreno-Jiménez E

  18. Effect of solution conductivity and electrode shape on the deposition of carbon nanotubes from solution using dielectrophoresis.

    PubMed

    Naieni, A Kashefian; Nojeh, A

    2012-12-14

    Dielectrophoresis (DEP) is a popular technique for fabricating carbon nanotube (CNT) devices. The electric current passing through the solution during DEP creates a temperature gradient, which results in electrothermal fluid flow because of the presence of the electric field. CNT solutions prepared with various methods can have different conductivities and the motion of the solution because of the electrothermal phenomenon can affect the DEP deposition differently in each case. We investigated the effect of this movement in solutions with various levels of conductivity through experiments as well as numerical modeling. Our results show that electrothermal motion in the solution can alter the deposition pattern of the nanotubes drastically for high conductivity solutions, while DEP remains the dominant force when a low conductivity (surfactant-free) solution is used. The extent of effectiveness of each force is discussed in the various cases and the fluid movement model is investigated using two- and three-dimensional finite element simulations. PMID:23165429

  19. Regioselective alkene carbon-carbon bond cleavage to aldehydes and chemoselective alcohol oxidation of allylic alcohols with hydrogen peroxide catalyzed by [cis-Ru(II)(dmp)2(H2O)2]2+ (dmp = 2,9-dimethylphenanthroline).

    PubMed

    Kogan, Vladimir; Quintal, Miriam M; Neumann, Ronny

    2005-10-27

    [reaction: see text] [cis-Ru(II)(dmp)2(H2O)2]2+ (dmp = 2,9-dimethylphenanthroline) was found to be a selective oxidation catalyst using hydrogen peroxide as oxidant. Thus, primary alkenes were very efficiently oxidized via direct carbon-carbon bond cleavage to the corresponding aldehydes as an alternative to ozonolysis. Secondary alkenes were much less reactive, leading to regioselective oxidation of substrates such as 4-vinylcyclohexene and 7-methyl-1,6-octadiene at the terminal position. Primary allylic alcohols were chemoselectively oxidized to the corresponding allylic aldehydes, e.g., geraniol to citral. PMID:16235952

  20. [Determination of low-carbon alcohols, aldehydes and ketones in aqueous products of Fischer-Tropsch synthesis by gas chromatography].

    PubMed

    Gai, Qingqing; Wu, Peng; Shi, Yulin; Bai, Yu; Long, Yinhua

    2015-01-01

    A method for the determination of low-carbon (C1-C8) alcohols, aldehydes and ketones in aqueous products of Fischer-Tropsch synthesis was developed by gas chromatography. It included the optimization of separation conditions, the precision and accuracy of determination, and the use of correction factors of the analytes to ethanol for quantification. The aqueous products showed that the correlation coefficients for ethanol in different content ranges were above 0.99, which means it had good linear correlations. The spiked recoveries in the aqueous samples of Fischer-Tropsch synthesis were from 93.4% to 109.6%. The accuracy of the method can satisfy the requirement for the analysis of the aqueous samples of Fischer-Tropsch synthesis. The results showed that the total mass fractions of the major low-carbon alcohols, aldehydes, ketones in aqueous products of Fischer-Tropsch synthesis were about 3%-12%, and the contents of ethanol were the highest (about 1.7%-7.3%). The largest share of the total proportion was n-alcohols, followed by isomeric alcohols, aldehydes and ketones were the lowest. This method is simple, fast, and has great significance for the analysis of important components in aqueous products of Fischer-Tropsch synthesis. PMID:25958675

  1. Conversion of C2-C4 alcohols over copper-containing catalysts on carbon and fluorocarbon fibers

    NASA Astrophysics Data System (ADS)

    Tveritinova, E. A.; Zhitnev, Yu. N.; Roshchina, T. M.; Lunin, V. V.

    2011-07-01

    Carbon and fluorocarbon fibers were used as carriers for the preparation of copper catalysts from copper oxalate as precursor. The catalytic properties of catalyst were studied in the reaction of the dehydrogenation of C2-C4 alcohols by the pulsed microcatalytic method. The effect of the copper content in the catalyst, the reaction temperature on the degree of conversion, and the relation of the reaction channels were studied. The electron microphotographs were obtained, specific surfaces were measured, and X-ray pictures and infrared spectra of catalysts were taken. The activity of the catalysts on the carbon and fluorocarbon fibers in the dehydration-dehydrogenation reactions of C2-C4 alcohols was comparatively estimated. It was shown that the selectivity of the products from the dehydrogenation reaction is higher for the Cu-fluorocarbon fiber catalyst.

  2. Tip-growth of aligned carbon nanotubes on cobalt catalyst supported by alumina using alcohol catalytic chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Bistamam, Mohd Shahril Amin; Azam, Mohd Asyadi

    Metal oxide layer helps to support carbon nanotubes (CNTs) aligned perpendicular as well as preventing the tip-growth which takes place due to the strong adhesion force between the catalyst and metal oxide. However, in this work we discovered tip-growth of aligned CNTs with Co as catalyst on thermally oxidized Al/SiO2/Si substrate system using simple alcohol catalytic chemical vapor deposition technique.

  3. Anomalous electrical transport properties of polyvinyl alcohol-multiwall carbon nanotubes composites below room temperature

    NASA Astrophysics Data System (ADS)

    Chakraborty, G.; Gupta, K.; Meikap, A. K.; Babu, R.; Blau, W. J.

    2011-02-01

    The dc and ac electrical transport property of polyvinyl alcohol-multiwall carbon nanotubes composites has been investigated within a temperature range 77≤T≤300 K and in the frequency range 20 Hz-1 MHz in presence as well as in absence of a transverse magnetic field up to 1 T. The dc conductivity follows variable range hopping model. The magnetoconductivity of the samples changes a sign from positive to negative with an increase in temperature which can be interpreted by the dominancy of the quantum interference effect over the wave function shrinkage effect. The ac conductivity follows a power law whereas the temperature dependence of frequency exponent s can be explained by correlated barrier hopping model. The dielectric behavior of the samples has been governed by the grain and grain boundary resistance and capacitance. The ac conductivity reduces with the application of magnetic field. Although the theoretical model to explain it, is still lacking, we may conclude that this is due to the increase in grain and grain boundary resistance by the application of magnetic field.

  4. Electrospun polyvinyl alcohol/carbon dioxide modified polyethyleneimine composite nanofiber scaffolds.

    PubMed

    Wu, Han-Bing; Bremner, David H; Nie, Hua-Li; Quan, Jing; Zhu, Li-Min

    2015-05-01

    A novel biocompatible polyvinyl alcohol/carbon dioxide modified polyethyleneimine (PVA/PEI-CO2) composite nanofiber was fabricated by a green and facile protocol, which reduces the cytotoxicity of PEI through the surface modification of the PEI with CO2. The (13)C NMR spectrum, elemental analysis, and TGA show that CO2 has been incorporated in the PEI surface resulting in a relatively stable structure. The resulting PVA/PEI-CO2 composite nanofibers have been characterized by attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), contact angle, and scanning electron microscopy (SEM). The results show that the average diameters of the nanofibers range from 265 ± 53 nm to 423 ± 80 nm. The cytotoxicity of PVA/PEI-CO2 composite nanofibers was assessed by cytotoxicity evaluation using the growth and cell proliferation of normal mice Schwann cells. SEM and the MTT assay demonstrated the promotion of cell growth and proliferation on the PVA/PEI-CO2 composite scaffold. It suggests that PEI-CO2 can have tremendous potential applications in biological material research. PMID:25540321

  5. The impedance characterization of Carbon Nanotubes - Fumed Silica Poly (vinyl alcohol) Composites

    NASA Astrophysics Data System (ADS)

    Othman, R. N.; Wilkinson, A. N.

    2016-06-01

    Carbon Nanotube (CNT) was grown on the surface of fumed silica via chemical vapor deposition (CVD) method. In this work, silica acted as a site that holds CNT together, which prevents further agglomeration during composite processing. Iron catalyst at different loading (7.5 wt. % up to 25 wt. %) was introduced via impregnation method to synthesize CNT at 1000°C, under methane flow. Floating catalyst method was used where ferrocene (2.5 wt. % and 5 wt. %) was used as starting reactants together with toluene at 760°C. The reaction time was set at 1 hour for both methods. It was later confirmed via SEM images that the floating catalyst method is more suitable to produce a large amount of CNTs. The sample synthesized via floating catalyst method at both 2.5 wt.% and 5 wt. % ferrocene was later used to prepare composites. Composite films of the particles in poly (vinyl alcohol) (PVOH) were cast and their TEM images show that the dispersion is indeed uniform. From impedance measurement, it was found that the particles synthesized via floating catalyst method were found to form an electrically-conductive percolated network with percolation threshold of 1 wt. %, obtained via percolation equation.

  6. Utilization of cation exchange resins for the isolation and separation of transplutonium elements from others in aqueous and non aqueous-alcohol solutions of hydrochloric and nitric acids

    SciTech Connect

    Guseva, L.I.; Tikhomirova, G.S.

    1985-07-01

    The authors study the sorption of several transplutonium and fission elements on cation exchange resins in relation to the acid concentration and content of alcohol in solution. They observe a significant increase in sorption of the TPE on the cation exchanges from nitric acid solutions containing more than 50% of alcohol. On the basis of the experimental results they determine the optimum conditions for the concentration of TPE on cation exchangers with their subsequent separation from certain fission and other elements by means of hydrochloric acid and nitric acid solutions.

  7. Enthalpy pair coefficients of interaction for DL-valine in aqueous solutions of polyatomic alcohols at 298 K

    NASA Astrophysics Data System (ADS)

    Mezhevoi, I. N.; Badelin, V. G.

    2013-12-01

    Integral enthalpies of dissolution Δsol H m of DL-valine are measured via calorimetry of dissolution in aqueous solutions of glycerol, ethylene glycol, and 1,2-propylene glycol. Standard values of the enthalpies of dissolution (Δsol H ○) and transfer (Δtr H ○) of amino acid from water to mixed solvent are calculated from the resulting experimental data. The enthalpy coefficients for pair interactions hxy of amino acid with polyatomic alcohol molecules are calculated using the McMillan-Meyer theory and have positive values. The obtained results are discussed in light of the theory of the predomination of various types of interactions in mixed solutions and the effect of structural features of interacting biomolecules on the thermochemical parameters of the dissolution of amino acids.

  8. Fabrication and processing of high-strength densely packed carbon nanotube yarns without solution processes.

    PubMed

    Liu, Kai; Zhu, Feng; Liu, Liang; Sun, Yinghui; Fan, Shoushan; Jiang, Kaili

    2012-06-01

    Defects of carbon nanotubes, weak tube-tube interactions, and weak carbon nanotube joints are bottlenecks for obtaining high-strength carbon nanotube yarns. Some solution processes are usually required to overcome these drawbacks. Here we fabricate ultra-long and densely packed pure carbon nanotube yarns by a two-rotator twisting setup with the aid of some tensioning rods. The densely packed structure enhances the tube-tube interactions, thus making high tensile strengths of carbon nanotube yarns up to 1.6 GPa. We further use a sweeping laser to thermally treat as-produced yarns for recovering defects of carbon nanotubes and possibly welding carbon nanotube joints, which improves their Young's modulus by up to ∼70%. The spinning and laser sweeping processes are solution-free and capable of being assembled together to produce high-strength yarns continuously as desired. PMID:22538869

  9. THE SOLAR NEBULA ON FIRE: A SOLUTION TO THE CARBON DEFICIT IN THE INNER SOLAR SYSTEM

    SciTech Connect

    Lee, Jeong-Eun; Bergin, Edwin A.; Nomura, Hideko E-mail: ebergin@umich.edu

    2010-02-10

    Despite a surface dominated by carbon-based life, the bulk composition of the Earth is dramatically carbon poor when compared to the material available at formation. Bulk carbon deficiency extends into the asteroid belt representing a fossil record of the conditions under which planets are born. The initial steps of planet formation involve the growth of primitive sub-micron silicate and carbon grains in the Solar Nebula. We present a solution wherein primordial carbon grains are preferentially destroyed by oxygen atoms ignited by heating due to stellar accretion at radii <5 AU. This solution can account for the bulk carbon deficiency in the Earth and meteorites, the compositional gradient within the asteroid belt, and for growing evidence for similar carbon deficiency in rocks surrounding other stars.

  10. Fabrication and processing of high-strength densely packed carbon nanotube yarns without solution processes

    NASA Astrophysics Data System (ADS)

    Liu, Kai; Zhu, Feng; Liu, Liang; Sun, Yinghui; Fan, Shoushan; Jiang, Kaili

    2012-05-01

    Defects of carbon nanotubes, weak tube-tube interactions, and weak carbon nanotube joints are bottlenecks for obtaining high-strength carbon nanotube yarns. Some solution processes are usually required to overcome these drawbacks. Here we fabricate ultra-long and densely packed pure carbon nanotube yarns by a two-rotator twisting setup with the aid of some tensioning rods. The densely packed structure enhances the tube-tube interactions, thus making high tensile strengths of carbon nanotube yarns up to 1.6 GPa. We further use a sweeping laser to thermally treat as-produced yarns for recovering defects of carbon nanotubes and possibly welding carbon nanotube joints, which improves their Young's modulus by up to ~70%. The spinning and laser sweeping processes are solution-free and capable of being assembled together to produce high-strength yarns continuously as desired.

  11. Extraction of palladium from acidic solutions with the use of carbon adsorbents

    SciTech Connect

    O.N. Kononova; N.G. Goryaeva; N.B. Dostovalova; S.V. Kachin; A.G. Kholmogorov

    2007-08-15

    We studied the sorption of palladium(II) on LKAU-4, LKAU-7, and BAU carbon adsorbents from model hydrochloric acid solutions and the solutions of spent palladium-containing catalysts. It was found that sorbents based on charcoal (BAU) and anthracite (LKAU-4) were characterized by high sorption capacities for palladium. The kinetics of the saturation of carbon adsorbents with palladium(II) ions was studied, and it was found that more than 60% of the initial amount of Pd(II) was recovered in a 1-h contact of an adsorbent with a model solution. This value for the solutions of spent catalysts was higher than 35%.

  12. Synthesis of size-selected Pt nanoparticles supported on sulfonated graphene with polyvinyl alcohol for methanol oxidation in alkaline solutions

    NASA Astrophysics Data System (ADS)

    Yang, Jen-Ming; Wang, Sheng-An; Sun, Chia-Liang; Ger, Ming-Der

    2014-05-01

    In this study, the size-selected platinum (Pt) nanoparticles are loaded on sulfonated graphene with polyvinyl alcohol (PVA) as the conductive polymer for fuel-cell applications. Methanol oxidation reactions and reliability of various catalysts based on carbon black, graphene, and sulfonated graphene catalyst supports are compared under alkaline conditions. When PVA is used as the conductive polymer in place of Nafion, both the electrochemical active surface area (ECSA) and the methanol oxidation property were superior, irrespective of the catalyst and support. On the other hand, the catalyst with Pt on sulfonated graphene (Pt/sG) outperforms those on other supports. For methanol oxidation, the catalyst decay occurs with a decay of only 9.06% for Pt/sG. It is suggested that the sulfonate functional group on graphene not only improves catalytic activity but can also enhance catalyst reliability.

  13. Surface heterogeneity effects of activated carbons on the kinetics of paracetamol removal from aqueous solution

    NASA Astrophysics Data System (ADS)

    Ruiz, B.; Cabrita, I.; Mestre, A. S.; Parra, J. B.; Pires, J.; Carvalho, A. P.; Ania, C. O.

    2010-06-01

    The removal of a compound with therapeutic activity (paracetamol) from aqueous solutions using chemically modified activated carbons has been investigated. The chemical nature of the activated carbon material was modified by wet oxidation, so as to study the effect of the carbon surface chemistry and composition on the removal of paracetamol. The surface heterogeneity of the carbon created upon oxidation was found to be a determinant in the adsorption capability of the modified adsorbents, as well as in the rate of paracetamol removal. The experimental kinetic data were fitted to the pseudo-second order and intraparticle diffusion models. The parameters obtained were linked to the textural and chemical features of the activated carbons. After oxidation the wettability of the carbon is enhanced, which favors the transfer of paracetamol molecules to the carbon pores (smaller boundary layer thickness). At the same time the overall adsorption rate and removal efficiency are reduced in the oxidized carbon due to the competitive effect of water molecules.

  14. The thermochemistry of solution of L-α-alanyl-L-α-alanine in water-alcohol mixtures at 298.15 K

    NASA Astrophysics Data System (ADS)

    Smirnov, V. I.; Badelin, V. G.

    2008-07-01

    The integral enthalpies of solution of L-α-alanyl-L-α-alanine in water-ethanol, water- n-propanol, and water-isopropanol mixtures were measured calorimetrically at alcohol concentrations x 2 ranging from 0 to 0.4 mole fractions. The standard enthalpy of peptide solution Δsol H o and transfer Δtr H o from water into a mixed solvent were calculated. The effect of the structure and properties of peptides and mixture composition on the enthalpy characteristics is discussed. The enthalpy coefficients of pair interactions h xy between L-α-alanyl-L-α-alanine and alcohol molecules were calculated; these coefficients were positive and increased in the series ethanol, n-propanol, isopropanol. The analysis performed allowed the differences in the thermodynamic characteristics of solution of L-α-alanyl-L-α-alanine and DL-α-alanyl-DL-α-alanine in water-alcohol mixtures to be determined.

  15. Nitrogen and carbon removal efficiency of a polyvinyl alcohol gel based moving bed biofilm reactor system.

    PubMed

    Gani, Khalid Muzamil; Singh, Jasdeep; Singh, Nitin Kumar; Ali, Muntjeer; Rose, Vipin; Kazmi, A A

    2016-01-01

    In this study, the effectiveness of polyvinyl alcohol (PVA) gel beads in treating domestic wastewater was investigated: a moving bed biofilm reactor (MBBR) configuration (oxic-anoxic and oxic) with 10% filling fraction of biomass carriers was operated in a continuously fed regime at temperatures of 25, 20, 15 and 6 °C with hydraulic retention times (HRTs) of 32 h, 18 h, 12 h and 9 h, respectively. Influent loadings were in the range of 0.22-1.22 kg N m(-3) d(-1) (total nitrogen (TN)), 1.48-7.82 kg chemical oxygen demand (COD) m(-3) d(-1) (organic) and 0.12-0.89 kg NH4(+)-N m(-3)d(-1) (ammonia nitrogen). MBBR performance resulted in the maximum TN removal rate of 1.22 kg N m(-3) d(-1) when the temperature and HRT were 6 °C and 9 h, respectively. The carbon removal rate at this temperature and HRT was 6.82 kg COD m(-3) d(-1). Ammonium removal rates ranged from 0.13 to 0.75 kg NH4(+)-N m(-3) d(-1) during the study. Total phosphorus and suspended solid removal efficiency ranged from 84 to 98% and 85 to 94% at an influent concentration of 3.3-7.1 mg/L and 74-356 mg/L, respectively. The sludge wasted from the MBBR exhibited light weight features characterized by sludge volume index value of 185 mL/g. Experimental data obtained can be useful in further developing the concept of PVA gel based wastewater treatment systems. PMID:27054722

  16. An Examination of Problems and Solutions Related to the Chronic "Revolving Door" Alcohol Abuser. DHSS Planning Guideline #1, Task Assignment #1.11. Long-Term Support, Chronic Alcoholism and Other Drug Abuse.

    ERIC Educational Resources Information Center

    Vick, John W.; Houden, Dorothy

    This report contains recommendations of a Wisconsin Task Assignment Steering Committee created to explore solutions to some significant problems facing adult chronic "revolving-detox-door" alcohol abusers (CRA's), persons with repeated admissions for detoxification services; and to examine the system that serves and funds them. This report is…

  17. A selection platform for carbon chain elongation using the CoA-dependent pathway to produce linear higher alcohols.

    PubMed

    Machado, Hidevaldo B; Dekishima, Yasumasa; Luo, Hao; Lan, Ethan I; Liao, James C

    2012-09-01

    Production of green chemicals and fuels using metabolically engineered organisms has been a promising alternative to petroleum-based production. Higher chain alcohols (C4-C8) are of interest because they can be used as chemical feedstock as well as fuels. Recently, the feasibility of n-hexanol synthesis using Escherichia coli has been demonstrated by extending the modified Clostridium CoA-dependent n-butanol synthesis pathway, thereby elongating carbon chain length via reactions in reversed β-oxidation, (or β-reduction). Here, we developed an anaerobic growth selection platform that allows selection or enrichment of enzymes for increased synthesis of C6 and C8 linear alcohols. Using this selection, we were able to improve the carbon flux towards the synthesis of C6 and C8 acyl-CoA intermediates. Replacement of the original enzyme Clostridium acetobutylicum Hbd with Ralstonia eutropha homologue PaaH1 increased production of n-hexanol by 10-fold. Further directed evolution by random mutagenesis of PaaH1 improved n-hexanol and n-octanol production. This anaerobic growth selection platform may be useful for selecting enzymes for production of long-chain alcohols and acids using this CoA-dependent pathway. PMID:22819734

  18. PROCESS FOR RECOVERY OF URANIUM AND VANADIUM FROM CARBONATE SOLUTIONS BY REDUCTION-PRECIPITATION

    DOEpatents

    Ellis, D.A.; Lindblom, R.O.

    1957-09-24

    A process employing carbonate leaching of ores and an advantageous methcd of recovering the uranium and vanadium from the leach solution is described. The uranium and vanadium can be precipitated from carbonate leach solutions by reaction with sodium amalgam leaving the leach solution in such a condition that it is economical to replenish for recycling. Such a carbonate leach solution is treated with a dilute sodium amalgam having a sodium concentration within a range of about 0.01 to 0.5% of sodium. Efficiency of the treatment is dependent on at least three additional factors, intimacy of contact of the amalgam with the leach solution, rate of addition of the amalgam and exclusion of oxygen (air).

  19. Adsorption of various alcohols on Illinois No. 6 coal in aqueous solutions

    SciTech Connect

    Kwon, K.C.; Rigby, R.R.

    1993-07-01

    Hydrophilicity, hydrophobicity and aromacity of Illinois {number_sign}6 coal in water are relatively determined by evaluating equilibrium physical/chemical adsorption of probe compounds on the coal. Experiments on equilibrium adsorption loadings of various additives on 60--200 mesh Illinois {number_sign}6 coal (DECS-2; Randolph county) were performed to investigate relatively surface properties of the coal at 25{degree}C. The additives include various alcohols, alkanes and aromatic compounds. The main objectives of this research are to evaluate relatively surface properties of raw coals, treated coals and coal minerals with the inverse liquid chromatography technique, using various probe compounds, to analyze flotation recoveries of coals with a micro-flotation apparatus in order to relate coal floatability to evaluated coal surface properties, and to delineate roles of coal-cleaning/handling additives with the inverse liquid chromatography technique.

  20. Hydroxyapatite wrapped multiwalled carbon nanotubes composite, a highly efficient template for palladium loading for electrooxidation of alcohols

    NASA Astrophysics Data System (ADS)

    Safavi, Afsaneh; Abbaspour, Abdolkarim; Sorouri, Mohsen

    2015-08-01

    A new electrocatalyst is introduced by loading palladium nanoparticles on the unique structured composite of hydroxyapatite and multiwalled carbon nanotubes. The structure and morphology of the designed electrocatalyst are characterized by X-ray diffraction analysis (XRD) and transmission electron microscopy (TEM). The efficiency of the resulted nanostructure is explored toward the electrooxidation of some common alcohols in alkaline media. The electrooxidation of ethylene glycol (EG) is explored more extensively which provides a large peak current density (more than 1810 mA mg-1Pd). Surprisingly, the efficiency of oxidation is maintained even for relatively high concentrations of EG. In terms of the current density and the onset potential, significant improvements are observed for the proposed structure versus hydroxyapatite free catalyst. The high efficiency of the proposed electrocatalyst is explained via the presence of hydroxyl rich surface of hydroxyapatite which causes a more effective oxidation of alcohols over the loaded Pd nanoparticles.

  1. Solution-based carbohydrate synthesis of individual solid, hollow, and porous carbon nanospheres using spray pyrolysis.

    PubMed

    Wang, Chengwei; Wang, Yuan; Graser, Jake; Zhao, Ran; Gao, Fei; O'Connell, Michael J

    2013-12-23

    A facile and scalable solution-based, spray pyrolysis synthesis technique was used to synthesize individual carbon nanospheres with specific surface area (SSA) up to 1106 m(2)/g using a novel metal-salt catalyzed reaction. The carbon nanosphere diameters were tunable from 10 nm to several micrometers by varying the precursor concentrations. Solid, hollow, and porous carbon nanospheres were achieved by simply varying the ratio of catalyst and carbon source without using any templates. These hollow carbon nanospheres showed adsorption of to 300 mg of dye per gram of carbon, which is more than 15 times higher than that observed for conventional carbon black particles. When evaluated as supercapacitor electrode materials, specific capacitances of up to 112 F/g at a current density of 0.1 A/g were observed, with no capacitance loss after 20,000 cycles. PMID:24274705

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

    NASA Astrophysics Data System (ADS)

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

    2016-09-01

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

  3. Alkaline solution absorption of carbon dioxide method and apparatus

    DOEpatents

    Hobbs, D.T.

    1991-01-01

    Disclosed is a method for measuring the concentration of hydroxides (or pH) in alkaline solutions, using the tendency of hydroxides to adsorb CO{sub 2}. The method comprises passing CO{sub 2} over the surface of an alkaline solution in a remote tank before and after measurements of the CO{sub 2} concentration. Comparison of the measurements yields the adsorption fraction from which the hydroxide concentration can be calculated using a correlation of hydroxide or pH to adsorption fraction. A schematic is given of a process system according to a preferred embodiment of the invention. 2 figs.

  4. Inhibition Effect of Dodecylamine on Carbon Steel Corrosion in Hydrochloric Acid Solution

    NASA Astrophysics Data System (ADS)

    Chen, Zhenyu; Huang, Ling; Qiu, Yubing; Guo, Xingpeng

    2012-12-01

    Dodecylamine spontaneously adsorbs on carbon steel via its polar group (-NH2) in hydrochloric acid solution. Furthermore, it forms a monolayer film on carbon steel surface. The inhibition mechanism of dodecylamine for carbon steel is geometric blocking effect. The adsorption of dodecylamine on carbon steel surface follows Arrhenius equation. The adsorption slightly increases activated energy, but greatly reduces pre-exponential factor value. Atomic force microscopy force curves indicate that at the area without adsorbed dodecylamine, no obvious adhere force occurs. At the area with adsorbed dodecylamine, however, an average 1.3 nN adhere force is observed.

  5. Fabrication of carbon nanowires by pyrolysis of aqueous solution of sugar within asbestos nanofibers

    NASA Astrophysics Data System (ADS)

    Butko, V. Yu.; Fokin, A. V.; Nevedomskii, V. N.; Kumzerov, Yu. A.

    2015-05-01

    Carbon nanowires have been fabricated by pyrolysis of an aqueous solution of sugar in nanochannels of asbestos fibers. Electron microscopy demonstrates that the diameter of these nanochannels corresponds to the diameter of the thinnest of the carbon nanowires obtained. Some of these nanowires have a graphite crystal lattice and internal pores. After asbestos is etched out, the carbon nanowires can retain the original shape of the asbestos fibers. Heating in an inert atmosphere reduces the electrical resistivity of the carbon nanowires to ˜0.035 Ω cm.

  6. Evaluation of solution-processable carbon-based electrodes for all-carbon solar cells.

    PubMed

    Ramuz, Marc P; Vosgueritchian, Michael; Wei, Peng; Wang, Chenggong; Gao, Yongli; Wu, Yingpeng; Chen, Yongsheng; Bao, Zhenan

    2012-11-27

    Carbon allotropes possess unique and interesting physical, chemical, and electronic properties that make them attractive for next-generation electronic devices and solar cells. In this report, we describe our efforts into the fabrication of the first reported all-carbon solar cell in which all components (the anode, active layer, and cathode) are carbon based. First, we evaluate the active layer, on standard electrodes, which is composed of a bilayer of polymer sorted semiconducting single-walled carbon nanotubes and C(60). This carbon-based active layer with a standard indium tin oxide anode and metallic cathode has a maximum power conversion efficiency of 0.46% under AM1.5 Sun illumination. Next, we describe our efforts in replacing the electrodes with carbon-based electrodes, to demonstrate the first all-carbon solar cell, and discuss the remaining challenges associated with this process. PMID:23113673

  7. Extraction of actinides into aqueous polyethylene glycol solutions from carbonate media in the presence of alizarin complexone

    SciTech Connect

    Molochnikova, N.P.; Frenkel', V.Ya.; Myasoedov, B.F.; Shkinev, V.M.; Spivakov, B.Ya.; Zolotov, Yu.A.

    1987-01-01

    Actinide extraction in a two-phase aqueous system based on polyethylene glycol from carbonate solutions of various compositions in presence of alizarin complexone is studied. It is shown that the nature of the alkali metals affects actinide extraction into the polyethylene glycol phase. Tri- and tetravalent actinides are extracted maximally from sodium carbonate solutions. Separation of actinides in different oxidation states is more effective in potassium carbonate solutions. The behavior of americium in different oxidation states in the system carbonate-polyethylene glycol-complexone is studied. The possibility of extraction separation of microamount of americium(V) from curium in carbonate solutions in presence of alizarin complexone is shown.

  8. Alcoholism and Alcohol Abuse

    MedlinePlus

    ... This means that their drinking causes distress and harm. It includes alcoholism and alcohol abuse. Alcoholism, or ... brain, and other organs. Drinking during pregnancy can harm your baby. Alcohol also increases the risk of ...

  9. Recycled Poly(vinyl alcohol) Sponge for Carbon Encapsulation of Size-Tunable Tin Dioxide Nanocrystalline Composites.

    PubMed

    Ma, Yue; Tai, Cheuk-Wai; Gustafsson, Torbjörn; Edström, Kristina

    2015-06-22

    The recycling of industrial materials could reduce their environmental impact and waste haulage fees and result in sustainable manufacturing. In this work, commercial poly(vinyl alcohol) (PVA) sponges are recycled into a macroporous carbon matrix to encapsulate size-tunable SnO2 nanocrystals as anode materials for lithium-ion batteries (LIBs) through a scalable, flash-combustion method. The hydroxyl groups present copiously in the recycled PVA sponges guarantee a uniform chemical coupling with a tin(IV) citrate complex through intermolecular hydrogen bonds. Then, a scalable, ultrafast combustion process (30 s) carbonizes the PVA sponge into a 3D carbon matrix. This PVA-sponge-derived carbon could not only buffer the volume fluctuations upon the Li-Sn alloying and dealloying processes but also afford a mixed conductive network, that is, a continuous carbon framework for electrical transport and macropores for facile electrolyte percolation. The best-performing electrode based on this composite delivers a rate performance up to 9.72 C (4 A g(-1) ) and long-term cyclability (500 cycles) for Li(+) ion storage. Moreover, cyclic voltammograms demonstrate the coexistence of alloying and dealloying processes and non-diffusion-controlled pseudocapacitive behavior, which collectively contribute to the high-rate Li(+) ion storage. PMID:26033927

  10. Effect of alcohol aggregation on the retention factors of chiral solutes with an amylose-based sorbent: modeling and implications for the adsorption mechanism.

    PubMed

    Tsui, Hung-Wei; Franses, Elias I; Wang, Nien-Hwa Linda

    2014-02-01

    Various displacement models in the literature have been widely used for understanding the adsorption mechanisms of solutes in various chromatography systems. The models were used for describing the often-observed linear plots of the logarithms of the retention factor versus the logarithms of the polar modifier concentration CI(0). The slopes of such a plot was inferred to be equal to the number of the displaced modifier molecules upon adsorption of one solute molecule, and were generally found to be greater than 1. In this study, the retention factors of four structurally related chiral solutes, ethyl lactate (EL), methyl mandelate (MM), benzoin (B), and pantolactone (PL), were measured for the amylose tris[(S)-α-methylbenzylcarbamate] sorbent, or AS, as a function of the concentration of isopropanol (IPA) in n-hexane. With increasing IPA concentration CI(0), the slopes increase from less than 1, at a concentration range from 0.13 to 1.3M, to slightly more than 1 at higher concentrations. Such slopes cannot be explained by the conventional retention models. It was found previously for monovalent solutes that such slopes can only be explained when the aggregation of the mobile phase modifier, isopropyl alcohol, was accounted for. A new retention model is presented here, accounting for alcohol aggregation, multivalent solute adsorption, multivalent solute-alcohol complexation, alcohol adsorption, and solute intra hydrogen-bonding, which occur in these four solutes. The slope is found to be controlled by three key dimensionless groups, the fraction of the sorbent binding sites covered by IPA, the fraction of the solute molecules in complex form, and the fraction of the IPA molecules in aggregate form. The limiting slope at a very high IPA concentration is equal to the value of (x+y)/n, where x is the number of the solute-sorbent binding sites and y is the number of the alcohol molecules in the solute-alcohol complex, and n is the alcohol aggregation number. The model

  11. Integrated ternary artificial nacre via synergistic toughening of reduced graphene oxide/double-walled carbon nanotubes/poly(vinyl alcohol)

    NASA Astrophysics Data System (ADS)

    Gong, Shanshan; Wu, Mengxi; Jiang, Lei; Cheng, Qunfeng

    2016-07-01

    The synergistic toughening effect of building blocks and interface interaction exists in natural materials, such as nacre. Herein, inspired by one-dimensional (1D) nanofibrillar chitin and two-dimensional (2D) calcium carbonate platelets of natural nacre, we have fabricated integrated strong and tough ternary bio-inspired nanocomposites (artificial nacre) successfully via the synergistic effect of 2D reduced graphene oxide (rGO) nanosheets and 1D double-walled carbon nanotubes (DWNTs) and hydrogen bonding cross-linking with polyvinyl alcohol (PVA) matrix. Moreover, the crack mechanics model with crack deflection by 2D rGO nanosheets and crack bridging by 1D DWNTs and PVA chains induces resultant artificial nacre exhibiting excellent fatigue-resistance performance. These outstanding characteristics enable the ternary bioinspired nanocomposites have many promising potential applications, for instance, aerospace, flexible electronics devices and so forth. This synergistic toughening strategy also provides an effective way to assemble robust graphene-based nanocomposites.

  12. Sulfidic photochemical passivation of GaAs surfaces in alcoholic solutions

    SciTech Connect

    Simonsmeier, T.; Ivankov, A.; Bauhofer, W.

    2005-04-15

    We report on a remarkable enhancement of the passivation effect of sulfidic solutions through illumination with above band gap light. Luminescence measurements on GaAs surfaces which have been illuminated during chemical passivation reveal in comparison to nonilluminated samples a further reduction of their surface density of states as well as a significantly increased stability of the passivation. Investigations with photoelectron spectroscopy show that illumination leads to a nearly complete removal of oxides on the surface. Measurements on Schottky diodes which have been manufactured with photochemically passivated GaAs indicate a noticeable decrease in band bending and a depinning of the Fermi level.

  13. Methods of pretreating comminuted cellulosic material with carbonate-containing solutions

    DOEpatents

    Francis, Raymond

    2012-11-06

    Methods of pretreating comminuted cellulosic material with an acidic solution and then a carbonate-containing solution to produce a pretreated cellulosic material are provided. The pretreated material may then be further treated in a pulping process, for example, a soda-anthraquinone pulping process, to produce a cellulose pulp. The pretreatment solutions may be extracted from the pretreated cellulose material and selectively re-used, for example, with acid or alkali addition, for the pretreatment solutions. The resulting cellulose pulp is characterized by having reduced lignin content and increased yield compared to prior art treatment processes.

  14. Electrochemical formation of hydroxide for enhancing carbon dioxide and acid gas uptake by a solution

    DOEpatents

    Rau, Gregory Hudson

    2012-05-15

    A system is described for forming metal hydroxide from a metal carbonate utilizing a water electrolysis cell having an acid-producing anode and a hydroxyl-producing cathode immersed in a water solution of sufficient ionic content to allow an electric current to pass between the hydroxyl-producing cathode and the acid-producing anode. A metal carbonate, in particular water-insoluble calcium carbonate or magnesium carbonate, is placed in close proximity to the acid-producing anode. A direct current electrical voltage is provided across the acid-producing anode and the hydroxyl-producing cathode sufficient to generate acid at the acid-producing anode and hydroxyl ions at the hydroxyl-producing cathode. The acid dissolves at least part of the metal carbonate into metal and carbonate ions allowing the metal ions to travel toward the hydroxyl-producing cathode and to combine with the hydroxyl ions to form the metal hydroxide. The carbonate ions travel toward the acid-producing anode and form carbonic acid and/or water and carbon dioxide. Among other uses, the metal hydroxide formed can be employed to absorb acid gases such as carbon dioxide from a gas mixture. The invention can also generate hydrogen and oxidative gases such as oxygen or chlorine.

  15. Removal of black carbon particles from experimental flue gas by surfactant solution in a new type of umbrella plate scrubber.

    PubMed

    Lu, Pei; Li, Caiting; Zeng, Guangming; Zhao, Yapei; Zhan, Qi; Song, Jingke; Fan, Xiaopeng

    2013-01-01

    Black carbon (BC) particles were removed from experimental flue gas by the surfactant solutions of sodium dodecylbenzene sulfonate (SDBS), hexadecyl trimethyl ammonium bromide (CTAB), fatty alcohol polyoxyethylene ether-9 (AEO-9) and polyoxy ethrlene nonyl phinyl ether-10 (TX-10), as well as AEO-9-SDBS, AEO-9-CTAB and SDBS-CTAB, in a new type of umbrella plate scrubber. Among the four independent surfactants, AEO-9 has the lowest surface tension, 35.9 mN/m, which resulted in the highest BC removal ratio among the alone surfactants. The experimental conditions were as follows: dust concentration = 3000 mg/m3; gas velocity = 14 m/s; liquid-gas ratio = 0.80 l/m3; and gas flow = 400 m3/h. When the mole ratio of the mixed surfactants was 1:1, the lowest surface tension could be detected among the studied mixed surfactants. According to the molecular interaction parameters (beta) and the mole ratio of surfactant 1 in the mixture (x1), the synergistic effects of AEO-9-SDBS and SDBS-CTAB solutions were obviously higher than those of AEO-9-TX-10 and AEO-9-CTAB. Therefore, AEO-9-SDBS solution had the lowest surface tension among the mixtures due to its beta < 0 and x1 = 0.85. The mixture solution of AEO-9-SDBS (1:1 mole ratio, 0.2 mmol/l) yielded the highest BC removal ratio, about 99.8%, and it was about 12% higher than that of only water, which was about 87.9%. The calculated critical micelle concentration was almost the same as that of the experimental concentration when the related equation was corrected by beta. PMID:23530320

  16. Optoelectronic ally automated system for carbon nanotubes synthesis via arc-discharge in solution

    SciTech Connect

    Bera, Debasis; Brinley, Erik; Kuiry, Suresh C.; McCutchen, Matthew; Seal, Sudipta; Heinrich, Helge; Kabes, Bradley

    2005-03-01

    The method of arc discharge in the solution is unique and inexpensive route for synthesis of the carbon nanotubes (CNTs), carbon onions, and other carbon nanostructures. Such a method can be used for in situ synthesis of CNTs decorated with nanoparticles. Herein, we report a simple and inexpensive optoelectronically automated system for arc discharge in solution synthesis of CNTs. The optoelectronic system maintains a constant gap between the two electrodes allowing a continuous synthesis of the carbon nanostructures. The system operates in a feedback loop consisting of an electrode-gap detector and an analog electronic unit, as controller. This computerized feeding system of the anode was used for in situ nanoparticles incorporated CNTs. For example, we have successfully decorated CNTs with ceria, silica, and palladium nanoparticles. Characterizations of nanostructures are performed using high-resolution transmission electron microscopy, scanning transmission electron microscopy, energy dispersive spectroscopy, and scanning electron microscopy.

  17. Optoelectronically automated system for carbon nanotubes synthesis via arc-discharge in solution

    NASA Astrophysics Data System (ADS)

    Bera, Debasis; Brinley, Erik; Kuiry, Suresh C.; McCutchen, Matthew; Seal, Sudipta; Heinrich, Helge; Kabes, Bradley

    2005-03-01

    The method of arc discharge in the solution is unique and inexpensive route for synthesis of the carbon nanotubes (CNTs), carbon onions, and other carbon nanostructures. Such a method can be used for in situ synthesis of CNTs decorated with nanoparticles. Herein, we report a simple and inexpensive optoelectronically automated system for arc discharge in solution synthesis of CNTs. The optoelectronic system maintains a constant gap between the two electrodes allowing a continuous synthesis of the carbon nanostructures. The system operates in a feedback loop consisting of an electrode-gap detector and an analog electronic unit, as controller. This computerized feeding system of the anode was used for in situ nanoparticles incorporated CNTs. For example, we have successfully decorated CNTs with ceria, silica, and palladium nanoparticles. Characterizations of nanostructures are performed using high-resolution transmission electron microscopy, scanning transmission electron microscopy, energy dispersive spectroscopy, and scanning electron microscopy.

  18. Density and viscosity of some partially carbonated aqueous alkanolamine solutions and their blends

    SciTech Connect

    Weiland, R.H.; Dingman, J.C.; Cronin, D.B.; Browning, G.J.

    1998-05-01

    Very little information is available concerning the effect of acid gas loading on the physical properties of amine-treating solutions flowing through the absorption and regeneration columns used in gas processing. The densities and viscosities of partially carbonated monoethanolamine (MEA), diethanolamine (DEA), and N-methyldiethanolamine (MDEA) solutions were measured at 298 K. With increasing carbon dioxide loadings, significant increases in both density and viscosity were observed. These results were combined with literature data to produce correlations for alkanolamine solution density and viscosity as a function of amine concentration, carbon dioxide loading, and temperature. The resulting single-amine correlations were used to predict the densities and viscosities of DEA + MDEA and MEA + MDEA blends. Predictions are compared with data measured for these blends.

  19. Minimally refined biomass fuel. [carbohydrate-water-alcohol mixture

    SciTech Connect

    Pearson, R.K.; Hirschfeld, T.B.

    1981-03-26

    A minimally refined fluid composition, suitable as a fuel mixture and derived from biomass material, is comprised of one or more water-soluble carbohydrates such as sucrose, one or more alcohols having less than four carbons, and water. The carbohydrate provides the fuel source; water-solubilizes the carbohydrate; and the alcohol aids in the combustion of the carbohydrate and reduces the viscosity of the carbohydrate/water solution. Because less energy is required to obtain the carbohydrate from the raw biomass than alcohol, an overall energy savings is realized compared to fuels employing alcohol as the primary fuel.

  20. Effect of UV and electrochemical surface treatments on the adsorption and reaction of linear alcohols on non-porous carbon fibre

    NASA Astrophysics Data System (ADS)

    Osbeck, S.; Ward, S.; Idriss, H.

    2013-04-01

    The adsorption properties of untreated, electrochemically treated and ultra-violet/ozone treated polyacrylonitrile based carbon fibres were investigated using temperature programmed desorption (TPD) on a series of linear alcohols as probes in order to understand its surface properties. Surface uptake was found to be sensitive to both the surface treatment and the nature of the adsorbates. Surface coverage increased with increasing alcohol chain due to the increase in their polarizability. It also increased with the level of surface oxygen of the fibres most likely because it facilitates the Osbnd H bond dissociation of the alcohol functional group. In addition, the desorption temperature (during TPD) tracked the surface oxygen levels (as determined from XPS O1s signal) suggesting increasing in the adsorption energy. The reactions of C1-C4 linear alcohols were also investigated on the surface of the fibre carbon. The main reaction was dehydrogenation to the corresponding aldehydes; the dehydration reaction to olefins was not observed. The dehydrogenation reaction was sensitive to the length of the alky chain. It was highest for methanol (to formaldehyde) and decreased with increasing the carbon number. Overall TPD of linear alcohols was shown to be a promising method for quantifying the level and strength of bonding occurring on carbon fibre surfaces.

  1. Enhanced selectivity for the electrochemical reduction of CO2 to alcohols in aqueous solution with nanostructured Cu-Au alloy as catalyst

    NASA Astrophysics Data System (ADS)

    Jia, Falong; Yu, Xinxing; Zhang, Lizhi

    2014-04-01

    Electrochemical reduction of CO2 in an aqueous 0.5 M KHCO3 solution is studied by use of novel nanostructured Cu-Au alloys, which are prepared through electrochemical deposition with a nanoporous Cu film (NCF) as template. Linear voltammetry results show that the as-synthesized Cu-Au alloys exhibit obvious catalysis towards electrochemical reduction of CO2. Further analysis of products reveals that faradic efficiencies of alcohols (methanol and ethanol) are greatly dependent on the nanostructures and compositions of Cu-Au alloys. It is expected that this work could provide new insight into the development of powerful electrocatalysts for reduction of CO2 to alcohols.

  2. Subaerial diagenesis of carbonate sediments: efficiency of the solution-reprecipitation process.

    PubMed

    Harris, W H; Matthews, R K

    1968-04-01

    Interaction between percolating groludwaters and aragonitic carbonate sediments within the vadose zone of the coral cap of Barbados, West Indies, results in dissolution of aragonite and concurrent reprecipitation as low-magnesium calcite. Comparison of the ratios of strontium to calcium in groundwater, aragonitic carbonate, and recrystallized calcite indicates that locally the solution-reprecipitation process is operating at an efficiency greater than 90 percent. PMID:17808784

  3. The thermochemical characteristics of solution of DL-α-alanylglycine and DL-α-alanylalanine in water-alcohol mixtures at 298.15 K

    NASA Astrophysics Data System (ADS)

    Smirnov, V. I.; Mezhevoi, I. N.; Badelin, V. G.

    2007-05-01

    The integral enthalpies of solution of DL-α-alanylglycine and DL-α-alanylalanine in water-ethanol, water-n-propanol, and water-isopropanol mixtures were measured calorimetrically at alcohol concentrations x 2 = 0-0.4 mole fractions. The standard enthalpies of solution (Δsol H°) of the peptides and their transfer (Δtr H°) from water into the mixed solvents were calculated. The influence of the structure and properties of the solutes and mixture composition on the enthalpy characteristics were considered. The Δsol H° = f(x 2) and Δtr H° = f(x 2) dependences were found to have extrema. The enthalpy coefficients of pair interactions (h xy ) between the peptide and alcohol molecules were calculated. The coefficients were positive and increased in the series ethanol, n-propanol, isopropanol.

  4. Chemical characterization of a potassium hydroxyapatite prepared by soaking in potassium chloride and carbonate solutions.

    PubMed

    Nordström, E G; Karlsson, K H

    1992-01-01

    A potassium-doped synthetic apatite was prepared by soaking hydroxyapatite in potassium carbonate and potassium chloride solutions. The hydroxyapatite was prepared by firing slip cast ceramic bodies in vacuum at 1100 degrees C. The conical ceramic samples and a crushed material of this were soaked in carbonate and chloride solutions for 2, 4, 6, and 8 weeks. Potassium, calcium, and phosphate were determined by direct current plasma emission spectroscopy. The carbonate content was determined by thermogravimetric analysis and chloride titrimetrically. After 2 weeks, one potassium ion substituted one calcium ion when soaked in a carbonate solution. When soaked in the chloride solution substitution occurred to the same extent. At phosphate sites the substitution of phosphate for carbonate occurred at one sixth of the sites after 2 weeks. Chloride incorporated one half of the OH-sites after 2 weeks. After 4 weeks about one chloride ion was found in the apatite, and after 6 weeks one and a half of the OH-sites were occupied by chloride ions. PMID:1483120

  5. Synthesis of higher alcohols from carbon monoxide and hydrogen in a slurry reactor

    SciTech Connect

    McCutchen, M.S.

    1992-08-28

    Higher, i.e. C{sub 2{sup +}}, alcohols are desired as gasoline additives, feedstocks for producing ethers and as alternative fuels for automobiles. In all cases, the backbone branching of an alcohol improves octane rating, which is essential for good engine performance. These types of branched, higher alcohols are the desired products for a process converting synthesis gas, a CO and H{sub 2} mixture, often generated from coal gasification. Based on this premise, promoted ZnCr oxide catalysts appear to be as one of the best avenues for further investigation. Once this investigation is complete, a natural extension is to replace the Cr in the ZnCr oxide catalyst with Mo and W, both in the same elemental triad with Cr. Mo has already been shown as an active HAS catalyst, both on a SiO{sub 2} support and in the MoS{sub 2} form. The three catalyst combinations, ZnMo, ZnW, and MnCr oxides will be tested in the stirred autoclave system. However, if none of the three indicate any comparable activity and/or selectivity toward higher alcohols as compared with other HAS catalysts, then an investigation of the effects of Cs promotion on the ZnCr oxide methanol catalysts will be executed.

  6. Solution and shock-induced exsolution of argon in vitreous carbon

    NASA Technical Reports Server (NTRS)

    Gazis, Carey; Ahrens, Thomas J.

    1991-01-01

    To add to the knowledge of noble gas solution and exsolution in carbonaceus material, experiments were performed on vitreous carbon. Ar-rich vitreous carbon samples were prepared under vapor-saturated conditions using argon as the pressurizing medium. Solubility data were obtained for temperatures of 773 to 973 K and pressures of 250 to 1500 bars. Up to 7 wt pct Ar was dissolved in the carbon. The solubility data were compared to a thermodynamic model of argon atoms dissolving into a fixed population of 'holes' in the carbon. Two variations of the model yielded estimates of the enthalpy of solution of Ar in vitreous carbon equal to about -4700 cal/mole. Preliminary shock experiments showed that 28 percent of the total argon was released by driving 4 GPa shocks into the argon-rich carbon. It was demonstrated that shock-induced argon loss is not simply caused by the impact-induced diminution of grain size. The present value of shock pressure required for partial impact devolatilization of Ar from carbon is below the range (5-30 GPa) at which H2O is released from phyllosilicates.

  7. Kinetic peculiarities of diamond crystallization in K-Na-Mg-Ca-Carbonate-Carbon melt-solution

    NASA Astrophysics Data System (ADS)

    Solopova, N. A.; Spivak, A. V.; Litvin, Yu. A.; Shiryaev, A. A.; Tsel'movich, V. A.; Nekrasov, A. N.

    2013-02-01

    The kinetic peculiarities of diamond crystallization in multicomponent K-Na-Mg-Ca-carbonate-carbon system have been studied in conditions of diamond stability at 1500-1800°C and 7.5-8.5 GPa. It has been established that the diamond phase nucleation density at a fixed temperature of 1600°C decreases from 1.3 × 105 nuclei/mm3 at 8.5 GPa to 3.7 × 103 nuclei/mm3 at 7.5 GPa. The fluorescence spectra of obtained diamond crystals contain peaks at 504 nm ( H3-defect), 575 nm (NV-center), and 638 nm (NV-defect), caused by the presence of nitrogen impurity. In the cathodoluminescence spectra, an A-band with the maximum at 470 nm is present. The obtained data make it possible to assign the synthesized diamonds in the carbonate-carbon system to the mixed Ia + Ib type.

  8. Importance of solute partitioning in biphasic oxidation of benzyl alcohol by free and immobilized whole cells of Pichia pastoris

    SciTech Connect

    Kawakami, Koei; Nakahara, Takehiko . Dept. of Chemical Engineering)

    1994-04-25

    Using free and immobilized whole cells of Pichia pastoris, the biocatalytic oxidation of benzyl alcohol was investigated in different two-phase systems. This reaction was strongly influenced by both the substrate and product inhibitions, and the production rate of benzaldehyde in the aqueous system became maximum at the initial substrate concentration of ca. 29 g/L with the aldehyde formation less than 4 to 5 g/L even after a longer reaction period. The reaction rates in the two-liquid phase systems were predominantly determined by the partitioning behaviors of the substrate and the product between the two phases rather than by enzyme deactivation by the organic solvents. In the two-liquid phase systems, consequently, the organic solvent acted as a reservoir to reduce these inhibitory effects, and it was essential to select the organic solvent providing the optimal partitioning of the substrate into the aqueous phase as well as the preferential extraction of the product into the organic phase. The whole cells immobilized in a mixed matrix composed of silicone polymer and Ca alginate gel worked well in the xylene and decane media, providing comparable activities with the free cells. The production rate of aldehyde was also influenced by the solute partitioning into the hydrophilic alginate phase where the cells existed.

  9. A new selective fluorene-based fluorescent internal charge transfer (ICT) sensor for sugar alcohols in aqueous solution.

    PubMed

    Hosseinzadeh, Rahman; Mohadjerani, Maryam; Pooryousef, Mona

    2016-03-01

    Sugar alcohols, such as sorbitol, are commonly used as a replacement for sucrose in the food industry, applied as starting material for vitamin C synthesis, and involved as one of the causative factors in diabetic complications. Therefore, their detection and quantification in aqueous solution are necessary. The reversible covalent interactions between boronic acids and diols are the basis of efficient methods for the detection of saccharides. Herein, we report a new internal charge transfer (ICT) fluorene-based fluorescent boronic acid sensor (1) 2-[(9,9-dimethyl-9H-fluoren-2-yl-amino)methyl] phenyl boronic acid that shows significant fluorescence changes upon addition of saccharides. The boronic acid has high affinity (K a = 1107.9 M(-1)) and selectivity for sorbitol at pH = 8.31. It showed a linear response toward sorbitol in the concentration range from 1.0 × 10(-5) to 6.0 × 10(-4) mol L(-1) with the detection limit of 7.04 × 10(-6) mol L(-1). Sensor 1 was used to detect sorbitol in real samples with good recovery. PMID:26758597

  10. Analyzing the kinetic response of tin oxide-carbon and tin oxide-CNT composites gas sensors for alcohols detection

    NASA Astrophysics Data System (ADS)

    Kamble, Vinayak; Umarji, Arun

    2015-03-01

    Tin oxide nanoparticles are synthesized using solution combustion technique and tin oxide - carbon composite thick films are fabricated with amorphous carbon as well as carbon nanotubes (CNTs). The x-ray diffraction, Raman spectroscopy and porosity measurements show that the as-synthesized nanoparticles are having rutile phase with average crystallite size ˜7 nm and ˜95 m2/g surface area. The difference between morphologies of the carbon doped and CNT doped SnO2 thick films, are characterized using scanning electron microscopy and transmission electron microscopy. The adsorption-desorption kinetics and transient response curves are analyzed using Langmuir isotherm curve fittings and modeled using power law of semiconductor gas sensors.

  11. Analyzing the kinetic response of tin oxide-carbon and tin oxide-CNT composites gas sensors for alcohols detection

    SciTech Connect

    Kamble, Vinayak Umarji, Arun

    2015-03-15

    Tin oxide nanoparticles are synthesized using solution combustion technique and tin oxide – carbon composite thick films are fabricated with amorphous carbon as well as carbon nanotubes (CNTs). The x-ray diffraction, Raman spectroscopy and porosity measurements show that the as-synthesized nanoparticles are having rutile phase with average crystallite size ∼7 nm and ∼95 m{sup 2}/g surface area. The difference between morphologies of the carbon doped and CNT doped SnO{sub 2} thick films, are characterized using scanning electron microscopy and transmission electron microscopy. The adsorption-desorption kinetics and transient response curves are analyzed using Langmuir isotherm curve fittings and modeled using power law of semiconductor gas sensors.

  12. Carbon-13 NMR characterization of actinyl(VI) carbonate complexes in aqueous solution

    SciTech Connect

    Clark, D.L.; Hobart, D.E.; Palmer, P.D.; Sullivan, J.C.; Stout, B.E.

    1992-07-01

    The uranyl(VI) carbonate system has been re-examined using {sup 13}C NMR of 99.9% {sup 13}C-enriched U{sup VI}O{sub 2} ({sup 13}CO{sub 3}){sub 3}{sup 4{minus}} in millimolar concentrations. By careful control of carbonate ion concentration, we have confirmed the existence of the trimer, and observed dynamic equilibrium between the monomer and the timer. In addition, the ligand exchange reaction between free and coordinated carbonate on Pu{sup VI}O{sub 2}({sup 13}CO{sub 3}){sub 3}{sup 4{minus}} and Am{sup VI}O{sub 2}({sup 13}CO{sub 3}){sub 3}{sup 4{minus}} systems has been examined by variable temperature {sup 13}C NMR line-broadening techniques {sup 13}C NMR line-broadening techniques. A modified Carr-Purcell-Meiboom-Gill NMR pulse sequence was written to allow for experimental determination of ligand exchange parameters for paramagnetic actinide complexes. Preliminary Eyring analysis has provided activation parameters of {Delta}G{sup {double_dagger}}{sub 295} = 56 kJ/M, {Delta}H{sup {double_dagger}} = 38 kJ/M, and {Delta}S{sup {double_dagger}} = {minus}60 J/M-K for the plutonyl triscarbonate system, suggesting an associative transition state for the plutonyl (VI) carbonate complex self-exchange reaction. Experiments for determination of the activation parameters for the americium (VI) carbonate system are in progress.

  13. Iridium nanoparticles supported on hierarchical porous N-doped carbon: an efficient water-tolerant catalyst for bio-alcohol condensation in water

    NASA Astrophysics Data System (ADS)

    Liu, Di; Chen, Xiufang; Xu, Guoqiang; Guan, Jing; Cao, Quan; Dong, Bo; Qi, Yunfei; Li, Chunhu; Mu, Xindong

    2016-02-01

    Nitrogen-doped hierarchical porous carbons were synthesized successfully by a controllable one-pot method using glucose and dicyandiamide as carbon source and nitrogen source via hydrothermal carbonization process. The nitrogen-doped materials, possessing high nitrogen content (up to 7 wt%), large surface area (>320 m2 g-1) and excellent hierarchical nanostructure, were employed as catalyst supports for immobilization of iridium nanoparticles for bio-alcohol condensation in water. The introduction of nitrogen atoms into the carbon framework significantly improved iridium nanoparticles dispersion and stabilization. The novel iridium catalysts exhibited superior catalytic activity in the aqueous phase condensation of butanol, offering high butanol conversion of 45% with impressive 2-ethylhexanol selectivity of 97%. The heterogeneous catalysts had great advantages of easy recovery and high catalytic stability. The outstanding catalytic performance could be attributed to excellent dispersion of iridium nanoparticles, stronger iridium-support interactions and interaction of nitrogen species with alcohol substrates.

  14. Iridium nanoparticles supported on hierarchical porous N-doped carbon: an efficient water-tolerant catalyst for bio-alcohol condensation in water

    PubMed Central

    Liu, Di; Chen, Xiufang; Xu, Guoqiang; Guan, Jing; Cao, Quan; Dong, Bo; Qi, Yunfei; Li, Chunhu; Mu, Xindong

    2016-01-01

    Nitrogen-doped hierarchical porous carbons were synthesized successfully by a controllable one-pot method using glucose and dicyandiamide as carbon source and nitrogen source via hydrothermal carbonization process. The nitrogen-doped materials, possessing high nitrogen content (up to 7 wt%), large surface area (>320 m2 g−1) and excellent hierarchical nanostructure, were employed as catalyst supports for immobilization of iridium nanoparticles for bio-alcohol condensation in water. The introduction of nitrogen atoms into the carbon framework significantly improved iridium nanoparticles dispersion and stabilization. The novel iridium catalysts exhibited superior catalytic activity in the aqueous phase condensation of butanol, offering high butanol conversion of 45% with impressive 2-ethylhexanol selectivity of 97%. The heterogeneous catalysts had great advantages of easy recovery and high catalytic stability. The outstanding catalytic performance could be attributed to excellent dispersion of iridium nanoparticles, stronger iridium-support interactions and interaction of nitrogen species with alcohol substrates. PMID:26912370

  15. Iridium nanoparticles supported on hierarchical porous N-doped carbon: an efficient water-tolerant catalyst for bio-alcohol condensation in water.

    PubMed

    Liu, Di; Chen, Xiufang; Xu, Guoqiang; Guan, Jing; Cao, Quan; Dong, Bo; Qi, Yunfei; Li, Chunhu; Mu, Xindong

    2016-01-01

    Nitrogen-doped hierarchical porous carbons were synthesized successfully by a controllable one-pot method using glucose and dicyandiamide as carbon source and nitrogen source via hydrothermal carbonization process. The nitrogen-doped materials, possessing high nitrogen content (up to 7 wt%), large surface area (>320 m(2) g(-1)) and excellent hierarchical nanostructure, were employed as catalyst supports for immobilization of iridium nanoparticles for bio-alcohol condensation in water. The introduction of nitrogen atoms into the carbon framework significantly improved iridium nanoparticles dispersion and stabilization. The novel iridium catalysts exhibited superior catalytic activity in the aqueous phase condensation of butanol, offering high butanol conversion of 45% with impressive 2-ethylhexanol selectivity of 97%. The heterogeneous catalysts had great advantages of easy recovery and high catalytic stability. The outstanding catalytic performance could be attributed to excellent dispersion of iridium nanoparticles, stronger iridium-support interactions and interaction of nitrogen species with alcohol substrates. PMID:26912370

  16. Solution-phase EPR studies of single-walled carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Chen, Y.; Chen, J.; Hu, H.; Hamon, M. A.; Itkis, M. E.; Haddon, R. C.

    1999-01-01

    We report EPR studies on pristine, purified, shortened and soluble SWNTs in various solution phases. Some of these samples give rise to strong, sharp EPR signals, and this technique is useful for monitoring the presence of SWNTs in aqueous and organic solvents. The soluble SWNTs carry about 1 unpaired electron per 10000 carbon atoms and give a free electron g-value.

  17. Sorption of metal ions from multicomponent aqueous solutions by activated carbons produced from waste

    SciTech Connect

    Tikhonova, L.P.; Goba, V.E.; Kovtun, M.F.; Tarasenko, Y.A.; Khavryuchenko, V.D.; Lyubchik, S.B.; Boiko, A.N.

    2008-08-15

    Activated carbons produced by thermal treatment of a mixture of sunflower husks, low-grade coal, and refinery waste were studied as adsorbents of transition ion metals from aqueous solutions of various compositions. The optimal conditions and the mechanism of sorption, as well as the structure of the sorbents, were studied.

  18. Radiolysis of Bicarbonate and Carbonate Aqueous Solutions: Product Analysis and Simulation of Radiolytic Processes

    SciTech Connect

    Cai Zhongli; Li Xifeng; Katsumura, Yosuke; Urabe, Osamu

    2001-11-15

    An understanding of the radiation-induced effects in groundwater is essential to evaluate the safe geological disposal of spent fuel. In groundwater, the bicarbonate ion is the predominant and common anion; this work investigated radiation-induced chemical reactions of (bi)carbonate aqueous solutions with steady-state irradiation and pulse radiolysis methods. Aqueous solutions of sodium (bi)carbonate as high as 50 mmol.dm{sup -3} were used. The formation of formate, oxalate, and H{sub 2}O{sub 2} were measured under different conditions. A complete set of reaction steps and reliable kinetic data for the radiolysis of (bi)carbonate aqueous solutions at ionic strength close to the groundwater were proposed. Kinetic calculations were completed based on the proposed reaction steps and the kinetic data obtained in the present work. The results from the calculation are in good agreement with the experimental results. With these proposed reaction steps and kinetic data, computer simulation can be performed to predict the yield of radiolytic products of (bi)carbonate aqueous solutions as a function of irradiation time and used to evaluate the safety of geological disposal options of spent fuel.

  19. Computer simulation of cascade damage in -iron with carbon in solution

    SciTech Connect

    Calder, Andrew F; Bacon, David J; Barashev, Aleksandr; Osetsky, Nickolai

    2008-01-01

    Computer simulation of cascade damage in -iron with carbon in solution Original Research Article Journal of Nuclear Materials, Volume 382, Issues 2 3, 1 December 2008, Pages 91-95 Andrew F. Calder, David J. Bacon, Alexander V. Barashev, Yuri N. Osetsky

  20. Two-dimensional numerical simulation of the red blood cell floating in a plasma-alcohol solution through stenosis in a microvessel

    NASA Astrophysics Data System (ADS)

    Ni, Aleksey; Cheema, Taqi Ahmad; Kwak, Moon Kyu; Park, Cheol Woo

    2014-08-01

    A two-dimensional computational model of a single red blood cell (RBC) floating in a plasma-alcohol solution through a microchannel with stenosis was created using the Arbitrary Lagrangian-Eulerian (ALE) method with moving mesh for a fluid structure interaction problem. Cell deformability and stability were studied in a plasma-alcohol solution at different fluid flow conditions during movement through the channel with stenosis. Different results were obtained for different input parameters. Motion through 45% and 70% stenoses with the high and law velocities of the RBC and different viscosities was analyzed and successfully simulated. Results show that changes in RBC deformability were due to the effects of alcohol. Changes in behavior during motion were also observed. At low shear rate and high surrounding fluid viscosity the RBC showed a tendency to rotate during movement. The proposed model with its coupling of structural and fluid analysis techniques could be useful to understand the effect of alcohol on the RBC passing through stenosis.

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

    PubMed

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

    2004-04-01

    Activated carbons were produced from several solid wastes, namely, waste PET, waste tires, refuse derived fuel and wastes generated during lactic acid fermentation from garbage. Activated carbons having various pore size distributions were obtained by the conventional steam-activation method and via the pre-treatment method (i.e., mixture of raw materials with a metal salt, carbonization and acid treatment prior to steam-activation) that was proposed by the authors. The liquid-phase adsorption characteristics of organic compounds from aqueous solution on the activated carbons were determined to confirm the applicability of these carbons, where phenol and a reactive dye, Black5, were employed as representative adsorbates. The hydrophobic surface of the carbons prepared was also confirmed by water vapor adsorption. The characteristics of a typical commercial activated carbon were also measured and compared. It was found that the activated carbons with plentiful mesopores prepared from PET and waste tires had quite high adsorption capacity for large molecules. Therefore they are useful for wastewater treatment, especially, for removal of bulky adsorbates. PMID:15026233

  2. a Search for Interstellar Carbon-Chain Alcohol HC4OH in the Star Forming Region L1527

    NASA Astrophysics Data System (ADS)

    Araki, Mitsunori; Takano, Shuro; Koshikawa, Hiromichi Yamabe Naohiro; Tsukiyama, Koichi; Nakane, Aya; Okabatyashi, Toshiaki; Kunimatsu, Arisa; Kuze, Nobuhiko

    2011-06-01

    We have made a sensitive search for the rotational transitions of carbon-chain alcohol HC_4OH with the frequency ragne from 21.2 to 46.7 GHz in the star forming region L1527 in Taurus with rich carbon-chain chemistry. The incentive of this observation was a laboratory detection of HC_4OH by the microwave spectroscopy. Despite achieving an rms of several mK in antenna temperature by the 45m telescope at Nobeyama Radio Observatory, the searche for HC_4OH was negative, leading to a 5 sigma upper limit corresponding to the column density of 4 × 1012 Cm-2 based on the excitation temperature of 12.3 K. The upper limit indicates that the [HC_4-OH]/[HC_4-CN] ratio is less than 1.0. The ratio suggests that the cyanide species with carbon-chain structure is dominant in comparison with the hydroxyl one in L1527, which can be the opposite case of saturated compounds, e.g. CH_3OH and CH_3CN, in hot cores and dark clouds.

  3. Atomic force microscopy and tribology study of the adsorption of alcohols on diamond-like carbon coatings and steel

    NASA Astrophysics Data System (ADS)

    Kalin, M.; Simič, R.

    2013-04-01

    Polar molecules are known to affect the friction and wear of steel contacts via adsorption onto the surface, which represents one of the fundamental boundary-lubrication mechanisms. Since the basic chemical and physical effects of polar molecules on diamond-like carbon (DLC) coatings have been investigated only very rarely, it is important to find out whether such molecules have a similar effect on DLC coatings as they do on steel. In our study the adsorption of hexadecanol in various concentrations (2-20 mmol/l) on DLC was studied under static conditions using an atomic force microscope (AFM). The amount of surface coverage, the size and the density of the adsorbed islands of alcohol molecules were analyzed. Tribological tests were also performed to correlate the wear and friction behaviours with the adsorption of molecules on the surface. In this case, steel surfaces served as a reference. The AFM was successfully used to analyze the adsorption ability of polar molecules onto the DLC surfaces and a good correlation between the AFM results and the tribological behaviour of the DLC and the steel was found. We confirmed that alcohols can adsorb physically and chemically onto the DLC surfaces and are, therefore, potential boundary-lubrication agents for the DLC coatings. The adsorption of alcohol onto the DLC surfaces reduces the wear of the coatings, but it is less effective in reducing the friction because of the already inherently low-friction properties of DLC. Tentative adsorption mechanisms that include the environmental species effect, the temperature effect and the tribological rubbing effect are proposed for DLC and steel surfaces.

  4. Precipitation of calcium carbonate in aqueous solutions in presence of ethylene glycol and dodecane.

    NASA Astrophysics Data System (ADS)

    Natsi, Panagiota D.; Rokidi, Stamatia; Koutsoukos, Petros G.

    2015-04-01

    The formation of calcium carbonate (CaCO3) in aqueous supersaturated solutions has been intensively studied over the past decades, because of its significance for a number of processes of industrial and environmental interest. In the oil and gas production industry the deposition of calcium carbonate affects adversely the productivity of the wells. Calcium carbonate scale deposits formation causes serious problems in water desalination, CO2 sequestration in subsoil wells, in geothermal systems and in heat exchangers because of the low thermal coefficient of the salt. Amelioration of the operational conditions is possible only when the mechanisms underlying nucleation and crystal growth of calcium carbonate in the aqueous fluids is clarified. Given the fact that in oil production processes water miscible and immiscible hydrocarbons are present the changes of the dielectric constant of the fluid phase has serious impact in the kinetics of calcium carbonate precipitation, which remains largely unknown. The problem becomes even more complicated if polymorphism exhibited by calcium carbonate is also taken into consideration. In the present work, the stability of aqueous solutions supersaturated with respect to all calcium carbonate polymorphs and the subsequent kinetics of calcium carbonate precipitation were measured. The measurements included aqueous solutions and solutions in the presence of water miscible (ethylene glycol, MEG) and water immiscible organics (n-dodecane). All measurements were done at conditions of sustained supersaturation using the glass/ Ag/AgCl combination electrode as a probe of the precipitation and pH as the master variable for the addition of titrant solutions with appropriate concentration needed to maintenance the solution supersaturation. Initially, the metastable zone width was determined from measurements of the effect of the solution supersaturation on the induction time preceding the onset of precipitation at free-drift conditions. The

  5. Synthesis of finely divided molybdenum sulfide nanoparticles in propylene carbonate solution

    SciTech Connect

    Afanasiev, Pavel

    2014-05-01

    Molybdenum sulfide nanoparticles have been prepared from the reflux solution reaction involving ammonium heptamolybdate and elemental sulfur in propylene carbonate. Addition to the reaction mixture of starch as a natural capping agent leads to lesser agglomeration and smaller size of the particles. Nanoparticles of MoS{sub x} (x≈4) of 10–30 nm size are highly divided and form stable colloidal suspensions in organic solvents. Mo K edge EXAFS of the amorphous materials shows rapid exchange of oxygen to sulfur in the molybdenum coordination sphere during the solution reaction. Thermal treatment of the amorphous sulfides MoS{sub x} under nitrogen or hydrogen flow at 400 °C allows obtaining mesoporous MoS{sub 2} materials with very high pore volume and specific surface area, up to 0.45 cm{sup 3}/g and 190 m{sup 2}/g, respectively. The new materials show good potential for the application as unsupported hydrotreating catalysts. - Graphical abstract: Solution reaction in propylene carbonate allows preparing weakly agglomerated molybdenum sulfide with particle size 20 nm and advantageous catalytic properties. - Highlights: • Solution reaction in propylene carbonate yields MoS{sub x} particles near 20 nm size. • Addition of starch as capping agent reduces particles size and hinder agglomeration. • EXAFS at Mo K edge shows rapid oxygen to sulfur exchange in the solution. • Thermal treatment leads to MoS{sub 2} with very high porosity and surface area.

  6. Characterization of Th carbonate solutions using XAS and implications for thermodynamic modeling

    SciTech Connect

    Hess, N.J.; Felmy, A.R.; Rai, D.; Conradson, S.D.

    1997-12-31

    The chemical behavior of actinide elements in tank solutions, in soil, and in groundwater is dependent upon the chemical species that form when aqueous solutions come in contact with the actinide compounds. In particular the chemical speciation of the reduced actinide oxidation states (III and IV) are important, for example, to DOE waste tank processing and, more generally, to nuclear waste disposal issues. Predicting the solubility of the actinides in these solutions requires identification of the strong aqueous complexes, such as carbonates and organic chelating agents, that can form in aqueous solution. Previous speciation work has often relied on indirect techniques such as potentiometric titrations or solubility measurements. Recent XAS experiments determine directly the speciation of the Th carbonato species of seven solutions under a range of carbonate concentrations and pH conditions. The presence of the pentacarbonato complex is confirmed and the complex`s stability at low carbonate concentrations is determined. These experimental results support a proposed thermodynamic model that describes the solubility of Th(IV) hydrous oxide in the aqueous Na{sup +}-HCO{sub 3}{sup {minus}}-CO{sub 3}{sup 2{minus}}-OH{sup {minus}}-ClO{sub 4}{sup {minus}}-H{sub 2}O system extending to high concentrations at 25 C. This model is relatively simple in that only two aqueous species are included Th(OH){sub 3}CO{sub 3}{sup {minus}} and Th(CO{sub 3}){sub 5}{sup 6{minus}}.

  7. Thermodynamic properties of aqueous-alcoholic solutions of sodium chloride. H2O-2-C3H7OH-NaCl

    NASA Astrophysics Data System (ADS)

    Veryaeva, E. S.; Konstantinova, N. M.; Mamontov, M. N.; Uspenskaya, I. A.

    2010-11-01

    The temperature-concentration dependences of the NaCl activity coefficient in aqueous solutions of isopropanol (propanol-2) at temperatures of 298.15 and 323.15 K (solution ionic force, 0.01 to 3 m; alcohol content, 10-60 wt %) were determined through the electromotive force method with an ion-selective electrode. A Pitzer model was used to mathematically describe the thermodynamic properties. The integral Gibbs energy of the solution formation of the H2O-2-C3H7OH-NaCl ternary system was performed according to Darken's method. The dissociation degree of salt in the investigated solutions was estimated using the literature data on the association constant of NaCl in aqueous-isopropanol solution.

  8. Bimetallic CuCo nanoparticles derived from hydrotalcite supported on carbon fibers for higher alcohols synthesis from syngas

    NASA Astrophysics Data System (ADS)

    Wang, Lianfang; Cao, Ang; Liu, Guilong; Zhang, Lihong; Liu, Yuan

    2016-01-01

    Higher alcohols synthesis (HAS) is a strong exothermal reaction which leads to the formation of hotspots on the catalysts and the hotspots result in poor selectivity, and Cu-Co based catalysts are one of the most promising to which the formation of Cu-Co alloy is critical. Therefore a new scheme was proposed, based on the excellent thermal conductivity of carbon fibers (CFs) and the uniform mixing of metal ions in layered double hydroxides (LDHs), the latter favors the formation of metallic alloy. Nanocomposites of LDHs and CFs were prepared by using co-precipitation method and used for HAS, and characterized by using FTIR, N2 adsorption-desorption, XRD, TPR, SEM and TEM techniques. In the composites, nanosheets with the typical LDHs morphology are perpendicularly grown on the surface of CFs while intersecting each other, creating a highly open and porous structure. After reduction, Cu-Co-alloy nanoparticles are formed from the LDHs. The resultant catalysts showed high activity and much high selectivity to higher alcohols. The reported methods can be expanded to prepare other LDHs/CFs composites.

  9. Adsorption of carbon dioxide by solution-plasma-synthesized heteroatom-doped carbon nanospheres

    NASA Astrophysics Data System (ADS)

    Thongwichit, Nanthiya; Li, Oi Lun Helena; Yaowarat, Wattanachai; Saito, Nagahiro; Suriyapraphadilok, Uthaiporn

    2016-01-01

    Porous carbon nanospheres (CNSs) synthesized by a plasma-in-liquid technique were applied as an adsorbent for CO2 adsorption. Two different types of aromatic solvents, benzene and pyridine, were used as precursors to generate CNSs. The prepared CNSs were carbonized and then activated with CO2 to obtain carbon materials with a suitable porous structure for CO2 adsorption. To improve CO2 adsorption capacity, activated CNSs were then chemically modified using different approaches of surface treatment, namely, HNO3 oxidation, amination without HNO3 preoxidation, and amination with HNO3 preoxidation. The CO2 adsorption capacities of the samples were investigated at 1 atm and 40 °C using a simultaneous thermal analyzer. It was found that the CO2 adsorption of CNSs was enhanced through the development of textural properties. All of the surface treatment approaches led to the increase in CO2 adsorption capacity of the activated CNSs owing to the presence of nitrogen or oxygen functional groups introduced onto the carbon surface during the treatment.

  10. First Molecular Dynamics simulation insight into the mechanism of organics adsorption from aqueous solutions on microporous carbons

    NASA Astrophysics Data System (ADS)

    Terzyk, Artur P.; Gauden, Piotr A.; Zieliński, Wojciech; Furmaniak, Sylwester; Wesołowski, Radosław P.; Klimek, Kamil K.

    2011-10-01

    The results of 84 MD simulations showing the influence of porosity and carbon surface oxidation on adsorption of three organic compounds from aqueous solutions on carbons are reported. Based on a model of 'soft' activated carbon, three carbon structures with gradually changed microporosity were created. Next, different number of surface oxygen groups was introduced. We observe quantitative agreement between simulation and experiment i.e. the decrease in adsorption from benzene down to paracetamol. Simulation results clearly demonstrate that the balance between porosity and carbon surface chemical composition in organics adsorption on carbons, and the pore blocking determine adsorption properties of carbons.

  11. Role of single-walled carbon nanotubes on ester hydrolysis and topography of electrospun bovine serum albumin/poly(vinyl alcohol) membranes.

    PubMed

    Ford, Ericka N J; Suthiwangcharoen, Nisaraporn; D'Angelo, Paola A; Nagarajan, Ramanathan

    2014-07-23

    Electrospun membranes were studied for the chemical deactivation of threat agents by means of enzymatic proteins. Protein loading and the surface chemistry of hybrid nanofibers influenced the efficacy by which embedded enzymes could digest the substrate of interest. Bovine serum albumin (BSA), selected as a model protein, was electrospun into biologically active fibers of poly(vinyl alcohol), PVA. Single-walled carbon nanotubes (SWNTs) were blended within these mixtures to promote protein assembly during the process of electrospinning and subsequently the ester hydrolysis of the substrates. The SWNT incorporation was shown to influence the topography of PVA/BSA nanofibers and enzymatic activity against paraoxon, a simulant for organophosphate agents and a phosphorus analogue of p-nitrophenyl acetate (PNA). The esterase activity of BSA against PNA was uncompromised upon its inclusion within nanofibrous membranes because similar amounts of PNA were hydrolyzed by BSA in solution and the electrospun BSA. However, the availability of BSA along the fiber surface was shown to affect the ester hydrolysis of paraoxon. Atomic force microscopy images of nanofibers implicated the surface migration of BSA during the electrospinning of SWNT filled dispersions, especially as greater weight fractions of protein were added to the spinning mixtures. In turn, the PVA/SWNT/BSA nanofibers outperformed the nanotube free PVA/BSA membranes in terms of paraoxon digestion. The results support the development of electrospun polymer nanofiber platforms, modulated by SWNTs for enzyme catalytic applications relevant to soldier protective ensembles. PMID:25007411

  12. The enthalpy of solution of DL-α-alanyl-DL-α-valine depending on the composition of water-alcohol binary solvents at 298.15 K

    NASA Astrophysics Data System (ADS)

    Smirnov, V. I.; Badelin, V. G.

    2008-12-01

    The integral enthalpies of solution of DL-α-alanyl-DL-α-valine in water-ethanol, water- n-propanol, and water-isopropanol mixtures at alcohol concentrations x 2 = 0-0.4 mole fractions were measured calorimetrically. The enthalpies of solution of the peptide Δsol H° and transfer from water to a mixed solvent Δtr H° were calculated. The effect of the structure and properties of the peptide and mixture composition on the enthalpy characteristics of the peptide are discussed. The enthalpy coefficients of pair interactions h xy of DL-α-alanyl-DL-α-valine with alcohol molecules were calculated. It was found that they were positive and increased in the series ethanol, n-propanol, isopropanol. An analysis of the results allows the general features of changes in the thermodynamic parameters of solution of peptides of the DL-α-alanine series with different amino acid residues in water-alcohol mixtures to be established.

  13. A palladium-doped ceria@carbon core-sheath nanowire network: a promising catalyst support for alcohol electrooxidation reactions

    NASA Astrophysics Data System (ADS)

    Tan, Qiang; Du, Chunyu; Sun, Yongrong; Du, Lei; Yin, Geping; Gao, Yunzhi

    2015-08-01

    A novel palladium-doped ceria and carbon core-sheath nanowire network (Pd-CeO2@C CSNWN) is synthesized by a template-free and surfactant-free solvothermal process, followed by high temperature carbonization. This hierarchical network serves as a new class of catalyst support to enhance the activity and durability of noble metal catalysts for alcohol oxidation reactions. Its supported Pd nanoparticles, Pd/(Pd-CeO2@C CSNWN), exhibit >9 fold increase in activity toward the ethanol oxidation over the state-of-the-art Pd/C catalyst, which is the highest among the reported Pd systems. Moreover, stability tests show a virtually unchanged activity after 1000 cycles. The high activity is mainly attributed to the superior oxygen-species releasing capability of Pd-doped CeO2 nanowires by accelerating the removal of the poisoning intermediate. The unique interconnected one-dimensional core-sheath structure is revealed to facilitate immobilization of the metal catalysts, leading to the improved durability. This core-sheath nanowire network opens up a new strategy for catalyst performance optimization for next-generation fuel cells.A novel palladium-doped ceria and carbon core-sheath nanowire network (Pd-CeO2@C CSNWN) is synthesized by a template-free and surfactant-free solvothermal process, followed by high temperature carbonization. This hierarchical network serves as a new class of catalyst support to enhance the activity and durability of noble metal catalysts for alcohol oxidation reactions. Its supported Pd nanoparticles, Pd/(Pd-CeO2@C CSNWN), exhibit >9 fold increase in activity toward the ethanol oxidation over the state-of-the-art Pd/C catalyst, which is the highest among the reported Pd systems. Moreover, stability tests show a virtually unchanged activity after 1000 cycles. The high activity is mainly attributed to the superior oxygen-species releasing capability of Pd-doped CeO2 nanowires by accelerating the removal of the poisoning intermediate. The unique

  14. Approximate Solutions for a Self-Folding Problem of Carbon Nanotubes

    SciTech Connect

    Y Mikata

    2006-08-22

    This paper treats approximate solutions for a self-folding problem of carbon nanotubes. It has been observed in the molecular dynamics calculations [1] that a carbon nanotube with a large aspect ratio can self-fold due to van der Waals force between the parts of the same carbon nanotube. The main issue in the self-folding problem is to determine the minimum threshold length of the carbon nanotube at which it becomes possible for the carbon nanotube to self-fold due to the van der Waals force. An approximate mathematical model based on the force method is constructed for the self-folding problem of carbon nanotubes, and it is solved exactly as an elastica problem using elliptic functions. Additionally, three other mathematical models are constructed based on the energy method. As a particular example, the lower and upper estimates for the critical threshold (minimum) length are determined based on both methods for the (5,5) armchair carbon nanotube.

  15. Electrochemical formation of hydroxide for enhancing carbon dioxide and acid gas uptake by a solution

    DOEpatents

    Rau, Gregory Hudson

    2014-07-01

    A system for forming metal hydroxide from a metal carbonate utilizes a water electrolysis cell having an acid-producing anode and a hydroxyl-producing cathode immersed in a water solution of sufficient ionic content to allow an electric current to pass between the hydroxyl-producing cathode and the acid-producing anode. A metal carbonate is placed in close proximity to the acid-producing anode. A direct current electrical voltage is provided across the acid-producing anode and the hydroxyl-producing cathode sufficient to generate acid at the acid-producing anode and hydroxyl ions at the hydroxyl-producing cathode. The acid dissolves at least part of the metal carbonate into metal and carbonate ions allowing the metal ions to travel toward the hydroxyl-producing cathode and to combine with the hydroxyl ions to form the metal hydroxide. The carbonate ions travel toward the acid-producing anode and form carbonic acid and/or water and carbon dioxide.

  16. Method for producing hydrocarbon and alcohol mixtures. [Patent application

    DOEpatents

    Compere, A.L.; Googin, J.M.; Griffith, W.L.

    1980-12-01

    It is an object of this invention to provide an efficient process for extracting alcohols and ketones from an aqueous solution containing the same into hydrocarbon fuel mixtures, such as gasoline, diesel fuel and fuel oil. Another object of the invention is to provide a mixture consisting of hydrocarbon, alcohols or ketones, polyoxyalkylene polymer and water which can be directly added to fuels or further purified. The above stated objects are achieved in accordance with a preferred embodiment of the invention by contacting an aqueous fermentation liquor with a hydrocarbon or hydrocarbon mixture containing carbon compounds having 5 to 18 carbon atoms, which may include gasoline, diesel fuel or fuel oil. The hydrocarbon-aqueous alcohol solution is mixed in the presence or one or more of a group of polyoxyalkylene polymers described in detail hereinafter; the fermentation alcohol being extracted into the hydrocarbon fuel-polyoxyalkylene polymer mixture.

  17. Performance evaluation of trimethylamine-carbon dioxide thermolytic draw solution for engineered osmosis

    SciTech Connect

    Boo, C; Khalil, YF; Elimelech, M

    2015-01-01

    We evaluated the performance of trimethylamine-carbon dioxide (TMA-CO2) as a potential thermolytic draw solution for engineered osmosis. Water flux and reverse solute flux with TMA-CO2 draw solution were measured in forward osmosis (FO) and pressure retarded osmosis (PRO) modes using thin-film composite (TFC) and cellulose triacetate (CTA) FO membranes. Water flux with the TMA-CO2 draw solution was comparable to that obtained with the more common ammonia-carbon dioxide (NH3-CO2) thermolytic draw solution at similar (1 M) concentration. Using a TFC-FO membrane, the water fluxes produced by 1 M TMA-CO2 and NH3-CO2 draw solutions with a DI water feed were, respectively, 33.4 and 35.6 L m(-2) h(-1) in PRO mode and 14.5 and 152 L m(-2) h(-1) in FO mode. Reverse draw permeation of TMA-CO2 was relatively low compared to NH3-CO2, ranging from 0.1 to 0.2 mol m(-2) h(-1) in all experiments, due to the larger molecular size of TMA. Thermal separation and recovery efficiency for TMA-CO2 was compared to NH3-CO2 by modeling low-temperature vacuum distillation utilizing low-grade heat sources. We also discuss possible challenges in the use TMA-CO2, including potential adverse impact on human health and environments. (C) 2014 Elsevier B.V. All rights reserved.

  18. Controls of carbonate mineralogy and solid-solution of Mg in calcite: evidence from spelean systems

    SciTech Connect

    Gonzalez, L.A.; Lohmann, K.C.

    1985-01-01

    Precipitation of carbonate minerals in spelean systems occurs under a wide range of fluid chemistry, Mg-Ca ratios, alkalinities, pH and temperatures; thus, spelean systems provide ideal settings to determine factors controlling the mineralogy of precipitated carbonates and solid-solution of Mg in calcite. Cave waters and actively-precipitating carbonate speleothems were collected from Carlsbad Caverns National Park, New Mexico and the Mammoth-Flint Cave System, Kentucky. Carbonate mineralogy of precipitated phases was determined by x-ray diffraction, and major and minor element composition of waters and accompanying minerals were determined by Atomic Absorption Spectrophotometry. Results demonstrate that at a constant CO3 concentration the precipitation threshold for calcite to aragonite is controlled dominantly by the Mg/Ca ratio of the ambient fluid. Aragonite precipitation is favored by high Mg/Ca ratios. Conversely, with increasing CO3 concentration at constant fluid Mg/Ca ratios, calcite is preferentially precipitated. Solid-solution of Mg in calcite is positively correlated with both increased Mg/Ca ratios and CO3 concentrations. These data suggest that Mg contents of calcite can not be defined solely in terms of a homogeneous distribution coefficient. Rather, Mg concentrations can be also be affected by the CO3 concentration and degree of calcite saturation, suggesting that the rate of crystal growth also plays and important role in Mg solid-solution in calcites.

  19. Collagen tissue treated with chitosan solutions in carbonic acid for improved biological prosthetic heart valves.

    PubMed

    Gallyamov, Marat O; Chaschin, Ivan S; Khokhlova, Marina A; Grigorev, Timofey E; Bakuleva, Natalia P; Lyutova, Irina G; Kondratenko, Janna E; Badun, Gennadii A; Chernysheva, Maria G; Khokhlov, Alexei R

    2014-04-01

    Calcification of bovine pericardium dramatically shortens typical lifetimes of biological prosthetic heart valves and thus precludes their choice for younger patients. The aim of the present work is to demonstrate that the calcification is to be mitigated by means of treatment of bovine pericardium in solutions of chitosan in carbonic acid, i.e. water saturated with carbon dioxide at high pressure. This acidic aqueous fluid unusually combines antimicrobial properties with absolute biocompatibility as far as at normal pressure it decomposes spontaneously and completely into H2O and CO2. Yet, at high pressures it can protonate and dissolve chitosan materials with different degrees of acetylation (in the range of 16-33%, at least) without any further pretreatment. Even exposure of the bovine pericardium in pure carbonic acid solution without chitosan already favours certain reduction in calcification, somewhat improved mechanical properties, complete biocompatibility and evident antimicrobial activity of the treated collagen tissue. The reason may be due to high extraction ability of this peculiar compressed fluidic mixture. Moreover, exposure of the bovine pericardium in solutions of chitosan in carbonic acid introduces even better mechanical properties and highly pronounced antimicrobial activity of the modified collagen tissue against adherence and biofilm formation of relevant Gram-positive and Gram-negative strains. Yet, the most important achievement is the detected dramatic reduction in calcification for such modified collagen tissues in spite of the fact that the amount of the thus introduced chitosan is rather small (typically ca. 1wt.%), which has been reliably detected using original tritium labelling method. We believe that these improved properties are achieved due to particularly deep and uniform impregnation of the collagen matrix with chitosan from its pressurised solutions in carbonic acid. PMID:24582232

  20. Solar-Driven Reduction of Aqueous Protons Coupled to Selective Alcohol Oxidation with a Carbon Nitride–Molecular Ni Catalyst System

    PubMed Central

    2016-01-01

    Solar water-splitting represents an important strategy toward production of the storable and renewable fuel hydrogen. The water oxidation half-reaction typically proceeds with poor efficiency and produces the unprofitable and often damaging product, O2. Herein, we demonstrate an alternative approach and couple solar H2 generation with value-added organic substrate oxidation. Solar irradiation of a cyanamide surface-functionalized melon-type carbon nitride (NCNCNx) and a molecular nickel(II) bis(diphosphine) H2-evolution catalyst (NiP) enabled the production of H2 with concomitant selective oxidation of benzylic alcohols to aldehydes in high yield under purely aqueous conditions, at room temperature and ambient pressure. This one-pot system maintained its activity over 24 h, generating products in 1:1 stoichiometry, separated in the gas and solution phases. The NCNCNx–NiP system showed an activity of 763 μmol (g CNx)−1 h–1 toward H2 and aldehyde production, a Ni-based turnover frequency of 76 h–1, and an external quantum efficiency of 15% (λ = 360 ± 10 nm). This precious metal-free and nontoxic photocatalytic system displays better performance than an analogous system containing platinum instead of NiP. Transient absorption spectroscopy revealed that the photoactivity of NCNCNx is due to efficient substrate oxidation of the material, which outweighs possible charge recombination compared to the nonfunctionalized melon-type carbon nitride. Photoexcited NCNCNx in the presence of an organic substrate can accumulate ultralong-lived “trapped electrons”, which allow for fuel generation in the dark. The artificial photosynthetic system thereby catalyzes a closed redox cycle showing 100% atom economy and generates two value-added products, a solar chemical, and solar fuel. PMID:27337491

  1. Solar-Driven Reduction of Aqueous Protons Coupled to Selective Alcohol Oxidation with a Carbon Nitride-Molecular Ni Catalyst System.

    PubMed

    Kasap, Hatice; Caputo, Christine A; Martindale, Benjamin C M; Godin, Robert; Lau, Vincent Wing-Hei; Lotsch, Bettina V; Durrant, James R; Reisner, Erwin

    2016-07-27

    Solar water-splitting represents an important strategy toward production of the storable and renewable fuel hydrogen. The water oxidation half-reaction typically proceeds with poor efficiency and produces the unprofitable and often damaging product, O2. Herein, we demonstrate an alternative approach and couple solar H2 generation with value-added organic substrate oxidation. Solar irradiation of a cyanamide surface-functionalized melon-type carbon nitride ((NCN)CNx) and a molecular nickel(II) bis(diphosphine) H2-evolution catalyst (NiP) enabled the production of H2 with concomitant selective oxidation of benzylic alcohols to aldehydes in high yield under purely aqueous conditions, at room temperature and ambient pressure. This one-pot system maintained its activity over 24 h, generating products in 1:1 stoichiometry, separated in the gas and solution phases. The (NCN)CNx-NiP system showed an activity of 763 μmol (g CNx)(-1) h(-1) toward H2 and aldehyde production, a Ni-based turnover frequency of 76 h(-1), and an external quantum efficiency of 15% (λ = 360 ± 10 nm). This precious metal-free and nontoxic photocatalytic system displays better performance than an analogous system containing platinum instead of NiP. Transient absorption spectroscopy revealed that the photoactivity of (NCN)CNx is due to efficient substrate oxidation of the material, which outweighs possible charge recombination compared to the nonfunctionalized melon-type carbon nitride. Photoexcited (NCN)CNx in the presence of an organic substrate can accumulate ultralong-lived "trapped electrons", which allow for fuel generation in the dark. The artificial photosynthetic system thereby catalyzes a closed redox cycle showing 100% atom economy and generates two value-added products, a solar chemical, and solar fuel. PMID:27337491

  2. RADIATION CHEMISTRY OF HIGH ENERGY CARBON, NEON AND ARGON IONS: INTEGRAL YIELDS FROM FERROUS SULFATE SOLUTIONS

    SciTech Connect

    Christman, E.A.; Appleby, A.; Jayko, M.

    1980-07-01

    Chemical yields of Fe{sup 3+} have been measured from FeSO{sub 4} solutions irradiated in the presence and absence of oxygen with carbon, neon, and argon ions from the Berkeley Bevalac facility. G(Fe{sup 3+}) decreases with increasing beam penetration and with increasing atomic number of the incident ion. The results are compared with current theoretical expectations of the behavior of these particles in an aqueous absorber. The chemical yields are consistently higher than theoretically predicted, by amounts varying from <6.2% (carbon ions) to <13.2% (argon ions). The additional yields are possibly attributable to fragmentation of the primary particle beams.

  3. Solution and precipitation hardening in carbon-doped two-phase {gamma}-titanium aluminides

    SciTech Connect

    Appel, F.; Christoph, U.; Wagner, R.

    1997-12-31

    A two-phase titanium aluminide alloy was systematically doped with carbon to improve its high temperature strength. Solid solutions and precipitates of carbon were formed by different thermal treatments. A fine dispersion of perovskite precipitates was found to be very effective for improving the high temperature strength and creep resistance of the material. The strengthening mechanisms were characterized by flow stresses and activation parameters. The investigations were accompanied by electron microscope observation of the defect structure which was generated during deformation. Special attention was paid on the interaction mechanisms of perfect and twinning dislocations with the carbide precipitates.

  4. Beyond temperature: Clumped isotope signatures in dissolved inorganic carbon species and the influence of solution chemistry on carbonate mineral composition

    NASA Astrophysics Data System (ADS)

    Tripati, Aradhna K.; Hill, Pamela S.; Eagle, Robert A.; Mosenfelder, Jed L.; Tang, Jianwu; Schauble, Edwin A.; Eiler, John M.; Zeebe, Richard E.; Uchikawa, Joji; Coplen, Tyler B.; Ries, Justin B.; Henry, Drew

    2015-10-01

    "Clumped-isotope" thermometry is an emerging tool to probe the temperature history of surface and subsurface environments based on measurements of the proportion of 13C and 18O isotopes bound to each other within carbonate minerals in 13C18O16O22- groups (heavy isotope "clumps"). Although most clumped isotope geothermometry implicitly presumes carbonate crystals have attained lattice equilibrium (i.e., thermodynamic equilibrium for a mineral, which is independent of solution chemistry), several factors other than temperature, including dissolved inorganic carbon (DIC) speciation may influence mineral isotopic signatures. Therefore we used a combination of approaches to understand the potential influence of different variables on the clumped isotope (and oxygen isotope) composition of minerals. We conducted witherite precipitation experiments at a single temperature and at varied pH to empirically determine 13C-18O bond ordering (Δ47) and δ18O of CO32- and HCO3- molecules at a 25 °C equilibrium. Ab initio cluster models based on density functional theory were used to predict equilibrium 13C-18O bond abundances and δ18O of different DIC species and minerals as a function of temperature. Experiments and theory indicate Δ47 and δ18O compositions of CO32- and HCO3- ions are significantly different from each other. Experiments constrain the Δ47-δ18O slope for a pH effect (0.011 ± 0.001; 12 ⩾ pH ⩾ 7). Rapidly-growing temperate corals exhibit disequilibrium mineral isotopic signatures with a Δ47-δ18O slope of 0.011 ± 0.003, consistent with a pH effect. Our theoretical calculations for carbonate minerals indicate equilibrium lattice calcite values for Δ47 and δ18O are intermediate between HCO3- and CO32-. We analyzed synthetic calcites grown at temperatures ranging from 0.5 to 50 °C with and without the enzyme carbonic anhydrase present. This enzyme catalyzes oxygen isotopic exchange between DIC species and is present in many natural systems. The two

  5. A novel one-pot and one-step microwave-assisted cyclization-methylation reaction of amino alcohols and acetylated derivatives with dimethyl carbonate and TBAC.

    PubMed

    Ochoa-Terán, Adrián; Guerrero, Leticia; Rivero, Ignacio A

    2014-01-01

    A simple and efficient microwave-assisted methodology for the synthesis of 4-substituted-3-methyl-1,3-oxazolidin-2-ones from amino alcohols catalyzed by a ionic liquid was developed. This novel one-pot and one-step cyclization-methylation reaction represents an easier and faster method than any other reported protocols that can be used to obtain the desired products in good yields and high purity. Applying microwave irradiation at 130°C in the presence of TBAC, dimethyl carbonate acts simultaneously as carbonylating and methylating agent and surprisingly promotes an in situ basic trans esterification when a N-acetylated amino alcohol is used as starting material. Furthermore, dimethyl carbonate worked better than diethyl carbonate in performing this reaction. PMID:25692177

  6. A Novel One-Pot and One-Step Microwave-Assisted Cyclization-Methylation Reaction of Amino Alcohols and Acetylated Derivatives with Dimethyl Carbonate and TBAC

    PubMed Central

    Ochoa-Terán, Adrián; Guerrero, Leticia; Rivero, Ignacio A.

    2014-01-01

    A simple and efficient microwave-assisted methodology for the synthesis of 4-substituted-3-methyl-1,3-oxazolidin-2-ones from amino alcohols catalyzed by a ionic liquid was developed. This novel one-pot and one-step cyclization-methylation reaction represents an easier and faster method than any other reported protocols that can be used to obtain the desired products in good yields and high purity. Applying microwave irradiation at 130°C in the presence of TBAC, dimethyl carbonate acts simultaneously as carbonylating and methylating agent and surprisingly promotes an in situ basic trans esterification when a N-acetylated amino alcohol is used as starting material. Furthermore, dimethyl carbonate worked better than diethyl carbonate in performing this reaction. PMID:25692177

  7. Environmentally benign formation of polymeric microspheres by rapid expansion of supercritical carbon dioxide solution with a nonsolvent.

    PubMed

    Matsuyama, K; Mishima, K; Umemoto, H; Yamaguchi, S

    2001-10-15

    A novel method is reported for forming polymer microparticles, which reduce atmospheric emissions of environmentally harmful volatile organic compounds such as toluene and xylene used as paint solvent in paint industry. The polymer microparticles have formed through rapid expansion from supercritical solution with a nonsolvent (RESS-N). Solubilization of poly(styrene)-b-(poly(methyl methacrylate)-co-poly (glycidyl methacrylate)) copolymer(PS-b-(PMMA-co-PGMA), MW = 5000, PS/PMMA/PGMA = 2/5/3), poly(ethylene glycol) (PEG, M. W = 4000), bisphenol A type epoxy resin (EP, MW = 3000), poly(methyl methacrylate) (PMMA; MW = 15000, 75000, 120000), and poly(oxyalkylene) alkylphenyl ether (MW = 4000) in carbon dioxide (CO2) was achieved with the use of small alcohols as cosolvents. The solubility of the PS-b-(PMMA-co-PGMA) is extremely low in either CO2 or ethanol but becomes 20 wt % in a mixture of the two. Because ethanol is a nonsolvent for the polymer, it can be used as a cosolvent in rapid expansion from supercritical solution to produce 1-3 microm particles that do not agglomerate. Obtained polymer particles by RESS-N were applied as powder coatings. The resulting coatings have a smooth and coherent film. The particle size distribution of microspheres was controlled by changing the polymer concentration, preexpansion pressure, temperature, and injection distance. The feed compositions were more effective than the other factors in controlling the particle size. The polymeric microparticles formed by RESS-N method can be utilized to make the thin coating film without anytoxic organic solvents and/or surfactants. PMID:11686380

  8. Selection of suitably non-repressing carbon sources for expression of alcohol oxidase isozyme promoters in the methylotrophic yeast Pichia methanolica.

    PubMed

    Nakagawa, Tomoyuki; Wakayama, Keishi; Hayakawa, Takashi

    2015-07-01

    In this work, we aimed to select suitable non-repressing carbon sources for the expression of promoters derived from the alcohol oxidase (AOD) isozyme genes, PMOD1 and PMOD2, during the growth of Pichia methanolica. Our results revealed that xylose is the best non-repressing carbon source for heterologous gene expression using both PMOD1 and PMOD2, and that glycerol is also a suitable carbon source with by which the on/off of PMOD2 expression can be controlled. PMID:25561326

  9. Flow injection analysis-isotope ratio mass spectrometry for bulk carbon stable isotope analysis of alcoholic beverages.

    PubMed

    Jochmann, Maik A; Steinmann, Dirk; Stephan, Manuel; Schmidt, Torsten C

    2009-11-25

    A new method for bulk carbon isotope ratio determination of water-soluble samples is presented that is based on flow injection analysis-isotope ratio mass spectrometry (FIA-IRMS) using an LC IsoLink interface. Advantages of the method are that (i) only very small amounts of sample are required (2-5 microL of the sample for up to 200 possible injections), (ii) it avoids complex sample preparation procedures such as needed for EA-IRMS analysis (only sample dilution and injection,) and (iii) high throughput due to short analysis times is possible (approximately 15 min for five replicates). The method was first tested and evaluated as a fast screening method with industrially produced ethanol samples, and additionally the applicability was tested by the measurement of 81 alcoholic beverages, for example, whiskey, brandy, vodka, tequila, and others. The minimal sample concentration required for precise and reproducible measurements was around 50 microL L(-1) ethanol/water (1.71 mM carbon). The limit of repeatability was determined to be r=0.49%. FIA-IRMS represents a fast screening method for beverage authenticity control. Due to this, samples can be prescreened as a decisive criterion for more detailed investigations by HPLC-IRMS or multielement GC-IRMS measurements for a verification of adulteration. PMID:19856915

  10. Static and dynamic adsorption of phenol from aqueous solution using spherical carbon

    NASA Astrophysics Data System (ADS)

    Bhargavi, R.; Kadirvelu, K.; Kumar, N. S.

    2013-06-01

    The objective of this work is to evaluate spherical carbon and modified spherical carbon for the removal of phenol from aqueous solution in static and dynamic studies under various conditions. It explores mainly two adsorbents, that is, activated spherical carbon (ASC) and modified activated spherical carbon (SSC). SEM characterization of both the adsorbents showed a clear change in the physical and chemical properties of the modified adsorbent from its precursor activated carbon. Both the adsorbents are subjected to static mode adsorption studies and after a comparison based on isotherm analysis; more efficient adsorbent is screened for column mode adsorption studies. The phenol removal increased for modified carbon. The aim of carrying out column mode studies will aid in ascertaining the practical applicability of the adsorbent in the real system and therefore, to assess the effect of various process variables, viz., bed height of the adsorbent, flow rate and initial concentration of the adsorbate on breakthrough time and adsorption capacity. The column studies generated data were modeled using the empirical relationship based on Bohart-Adams model. At the end, the option of regenerating the adsorbent was also explored using sodium hydroxide with the aim of minimize the hazardous generated and also to reuse the adsorbent material for many cycles without affecting original properties. Adsorbent regeneration efficiency of 72% was achieved. This investigation reveals that the material used as an adsorbent is very effective with high adsorption capacities and also possible to use in the real contaminated system.

  11. Determination of electronic states of individually dissolved ( n, m) single-walled carbon nanotubes in solution

    NASA Astrophysics Data System (ADS)

    Tanaka, Yasuhiko; Hirayama, Kohei; Niidome, Yasuro; Nakashima, Naotoshi

    2009-11-01

    Solution redox chemistry is useful to understand the chirality-dependent electronic properties of single-walled carbon nanotubes (SWNTs). We have found that the electron transfer reactions of sodium dithionite with SWNTs cause photoluminescence (PL) quenching processes of 14 individually dissolved SWNTs in an aqueous micellar solution. Based on the analysis using the Nernst equation for the PL change, we have determined the conduction band ( c1) levels of the 14 isolated SWNTs. We have also estimated the valence band ( ν1) levels as well as the Fermi levels of the SWNTs using the reported bandgap values of the corresponding isolated SWNTs.

  12. Solubility of mixtures of hydrogen sulfide and carbon dioxide in aqueous N-methyldiethanolamine solutions

    SciTech Connect

    Jou, Fang Yuan; Carroll, J.J.; Mather, A.E.; Otto, F.D. . Dept. of Chemical Engineering)

    1993-01-01

    Aqueous solutions of alkanolamines are commonly used to strip acid gases (H[sub 2]S and CO[sub 2]) from streams contaminated with these components. The two most widely used amines are monoethanolamine (MEA) and diethanolamine (DEA). The solubilities of mixtures of hydrogen sulfide and carbon dioxide in a 35 wt% (3.04 kmol/m[sup 3]) aqueous solution of N-methyldiethanolamine at 40 and 100C have been measured. Partial pressures of the acid gases ranged from 0.006 to 101 kPa at 40C and from 4 to 530 kPa at 100C.

  13. Redox-triggered C-C coupling of alcohols and vinyl epoxides: diastereo- and enantioselective formation of all-carbon quaternary centers via tert-(hydroxy)-prenylation.

    PubMed

    Feng, Jiajie; Garza, Victoria J; Krische, Michael J

    2014-06-25

    Iridium catalyzed primary alcohol oxidation triggers reductive C-O bond cleavage of isoprene oxide to form aldehyde-allyliridium pairs that combine to form products of tert-(hydroxy)-prenylation, a motif found in >2000 terpenoid natural products. Curtin-Hammett effects are exploited to enforce high levels of anti-diastereo- and enantioselectivity in the formation of an all-carbon quaternary center. The present redox-triggered carbonyl additions occur in the absence of stoichiometric byproducts, premetalated reagents, and discrete alcohol-to-aldehyde redox manipulations. PMID:24915473

  14. Platinum-palladium bimetallic nanoparticles on graphitic carbon nitride modified carbon black: A highly electroactive and durable catalyst for electrooxidation of alcohols

    NASA Astrophysics Data System (ADS)

    Qian, Huayu; Chen, Shouwen; Fu, Yongsheng; Wang, Xin

    2015-12-01

    A composite catalyst consisting of Pt-Pd bimetallic nanoparticles (NPs) and graphitic carbon nitride (g-C3N4) modified carbon black (CB) is designed and fabricated by a facile two-step approach. The resulting catalyst exhibits unprecedented high catalytic activity and excellent long-term stability for electrooxidation of alcohols (methanol, ethanol, ethylene glycol and glycerol) in alkaline media. The superior electrochemical performance of the composite catalyst is attributed to the specific characteristics of the unique nanostructure and the synergistic effects of individual components, including the complementary roles of Pt (dehydrogenation site) and Pd (removal of CO-like species), the template effect of the planar amino group of g-C3N4 for the dispersed decoration of Pt-Pd NPs, the high specific surface area of CB for the rapid diffusion of electrolyte and removal of the carbonaceous intermediates, as well as the structural stability of the support based on covalent interaction between g-C3N4 and CB for maintaining the durability of the catalytic system.

  15. Separation of surfactant functionalized single-walled carbon nanotubes via free solution electrophoresis method

    NASA Astrophysics Data System (ADS)

    Scheibe, Blazej; Rümmeli, Mark H.; Borowiak-Palen, Ewa; Kalenczuk, Ryszard J.

    2011-04-01

    This work presents the application of the free solution electrophoresis method (FSE) in the metallic / semiconductive (M/S) separation process of the surfactant functionalized single-walled carbon nanotubes (SWCNTs). The SWCNTs synthesized via laser ablation were purified through high vacuum annealing and subsequent refluxing processes in aqua regia solution. The purified and annealed material was divided into six batches. First three batches were dispersed in anionic surfactants: sodium dodecyl sulfate (SDS), sodium cholate (SC) and sodium deoxycholate (DOC). The next three batches were dispersed in cationic surfactants: cetrimonium bromide (CTAB), benzalkonium chloride (BKC) and cetylpyridinium chloride (CPC). All the prepared SWCNTs samples were subjected to FSE separation process. The fractionated samples were recovered from control and electrode areas and annealed in order to remove the adsorbed surfactants on carbon nanotubes (CNTs) surface. The changes of the van Hove singularities (vHS) present in SWCNTs spectra were investigated via UV-Vis-NIR optical absorption spectroscopy (OAS).

  16. Changing fluxes of carbon and other solutes from the Mekong River

    PubMed Central

    Li, Siyue; Bush, Richard T.

    2015-01-01

    Rivers are an important aquatic conduit that connects terrestrial sources of dissolved inorganic carbon (DIC) and other elements with oceanic reservoirs. The Mekong River, one of the world’s largest rivers, is firstly examined to explore inter-annual fluxes of dissolved and particulate constituents during 1923–2011 and their associated natural or anthropogenic controls. Over this period, inter-annual fluxes of dissolved and particulate constituents decrease, while anthropogenic activities have doubled the relative abundance of SO42−, Cl− and Na+. The estimated fluxes of solutes from the Mekong decrease as follows (Mt/y): TDS (40.4) > HCO3− (23.4) > Ca2+ (6.4) > SO42− (3.8) > Cl− (1.74)~Na+ (1.7) ~ Si (1.67) > Mg2+ (1.2) > K+ (0.5). The runoff, land cover and lithological composition significantly contribute to dissolved and particulate yields globally. HCO3− and TDS yields are readily predicted by runoff and percent of carbonate, while TSS yield by runoff and population density. The Himalayan Rivers, including the Mekong, are a disproportionally high contributor to global riverine carbon and other solute budgets, and are of course underlined. The estimated global riverine HCO3− flux (Himalayan Rivers included) is 34014 × 109 mol/y (0.41 Pg C/y), 3915 Mt/y for solute load, including HCO3−, and 13553 Mt/y for TSS. Thereby this study illustrates the importance of riverine solute delivery in global carbon cycling. PMID:26522820

  17. Changing fluxes of carbon and other solutes from the Mekong River.

    PubMed

    Li, Siyue; Bush, Richard T

    2015-01-01

    Rivers are an important aquatic conduit that connects terrestrial sources of dissolved inorganic carbon (DIC) and other elements with oceanic reservoirs. The Mekong River, one of the world's largest rivers, is firstly examined to explore inter-annual fluxes of dissolved and particulate constituents during 1923-2011 and their associated natural or anthropogenic controls. Over this period, inter-annual fluxes of dissolved and particulate constituents decrease, while anthropogenic activities have doubled the relative abundance of SO4(2-), Cl(-) and Na(+). The estimated fluxes of solutes from the Mekong decrease as follows (Mt/y): TDS (40.4) > HCO3(-) (23.4) > Ca(2+) (6.4) > SO4(2-) (3.8) > Cl(-) (1.74)~Na(+) (1.7) ~ Si (1.67) > Mg(2+) (1.2) > K(+ 0.5). The runoff, land cover and lithological composition significantly contribute to dissolved and particulate yields globally. HCO3(-) and TDS yields are readily predicted by runoff and percent of carbonate, while TSS yield by runoff and population density. The Himalayan Rivers, including the Mekong, are a disproportionally high contributor to global riverine carbon and other solute budgets, and are of course underlined. The estimated global riverine HCO3(-) flux (Himalayan Rivers included) is 34,014 × 10(9) mol/y (0.41 Pg C/y), 3915 Mt/y for solute load, including HCO3(-), and 13,553 Mt/y for TSS. Thereby this study illustrates the importance of riverine solute delivery in global carbon cycling. PMID:26522820

  18. Changing fluxes of carbon and other solutes from the Mekong River

    NASA Astrophysics Data System (ADS)

    Li, Siyue; Bush, Richard T.

    2015-11-01

    Rivers are an important aquatic conduit that connects terrestrial sources of dissolved inorganic carbon (DIC) and other elements with oceanic reservoirs. The Mekong River, one of the world’s largest rivers, is firstly examined to explore inter-annual fluxes of dissolved and particulate constituents during 1923-2011 and their associated natural or anthropogenic controls. Over this period, inter-annual fluxes of dissolved and particulate constituents decrease, while anthropogenic activities have doubled the relative abundance of SO42-, Cl- and Na+. The estimated fluxes of solutes from the Mekong decrease as follows (Mt/y): TDS (40.4) > HCO3- (23.4) > Ca2+ (6.4) > SO42- (3.8) > Cl- (1.74)~Na+ (1.7) ~ Si (1.67) > Mg2+ (1.2) > K+ (0.5). The runoff, land cover and lithological composition significantly contribute to dissolved and particulate yields globally. HCO3- and TDS yields are readily predicted by runoff and percent of carbonate, while TSS yield by runoff and population density. The Himalayan Rivers, including the Mekong, are a disproportionally high contributor to global riverine carbon and other solute budgets, and are of course underlined. The estimated global riverine HCO3- flux (Himalayan Rivers included) is 34014 × 109 mol/y (0.41 Pg C/y), 3915 Mt/y for solute load, including HCO3-, and 13553 Mt/y for TSS. Thereby this study illustrates the importance of riverine solute delivery in global carbon cycling.

  19. FILM FORMATION ON LITHIUM IN PROPYLENE CARBONATE SOLUTIONS UNDER OPEN CIRCUIT CONDITIONS

    SciTech Connect

    Geronov, Y.; Schwager, F.; Muller, R.H.

    1980-06-01

    The nature of protective surface layers formed on lithium in propylene carbonate solutions of LiClO{sub 4} and LiAsF{sub 6} at open circuit has been investigated by electrochemical pulse measurements. The results are consistent with the fastformation of a compact thin layer resulting from the reaction with residual water. This layer acts as a solid ionicconductor. Slow corrosion or decomposition processes produce a thicker porous overlayer.

  20. Electrochemical studies of the film formation on lithium in propylene carbonate solutions under open circuit conditions

    SciTech Connect

    Geronov, Y.; Schwager, F.; Muller, R.H.

    1981-04-01

    The nature of protective surface layers formed on lithium in propylene carbonate solutions of LiClO/sub 4/ and LiAsF/sub 6/ at open circuit has been investigated by electrochemical pulse measurements and other techniques. The results are consistent with the fast formation of a compact thin layer of Li/sub 2/O by reaction with residual water. This layer acts as a solid ionic conductor. Slow corrosion processes produce a thicker porous overlayer.

  1. Mechanism of Pitting Corrosion Prevention by Nitrite in Carbon Steel Exposed to Dilute Salt Solutions

    SciTech Connect

    Philip E. Zapp; John W. Van Zee

    2002-02-01

    The research has developed a broad fundamental understanding of the inhibition action of nitrite ions in preventing nitrate pitting corrosion of carbon steel tanks containing high-level radioactive waste. This fundamental understanding can be applied to specific situations during waste removal for permanent disposition and waste tank closure to ensure that the tanks are maintained safely. The results of the research provide the insight necessary to develop solutions that prevent further degradation.

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

    PubMed Central

    Erdem, Murat; Ucar, Suat; Karagöz, Selhan; Tay, Turgay

    2013-01-01

    The removal of lead (II) ions from aqueous solutions was carried out using an activated carbon prepared from a waste biomass. The effects of various parameters such as pH, contact time, initial concentration of lead (II) ions, and temperature on the adsorption process were investigated. Energy Dispersive X-Ray Spectroscopy (EDS) analysis after adsorption reveals the accumulation of lead (II) ions onto activated carbon. The Langmuir and Freundlich isotherm models were applied to analyze equilibrium data. The maximum monolayer adsorption capacity of activated carbon was found to be 476.2 mg g−1. The kinetic data were evaluated and the pseudo-second-order equation provided the best correlation. Thermodynamic parameters suggest that the adsorption process is endothermic and spontaneous. PMID:23853528

  3. Nanofiltration of Electrolyte Solutions by Sub-2nm Carbon Nanotube Membranes

    SciTech Connect

    Fornasiero, F; Park, H G; Holt, J K; Stadermann, M; Kim, S; In, J B; Grigoropoulos, C P; Noy, A; Bakajin, O

    2008-03-13

    Both MD simulations and experimental studies have shown that liquid and gas flow through carbon nanotubes with nanometer size diameter is exceptionally fast. For applications in separation technology, selectivity is required together with fast flow. In this work, we use pressure-driven filtration experiments to study ion exclusion in silicon nitride/sub-2-nm CNT composite membranes as a function of solution ionic strength, pH, and ion valence. We show that carbon nanotube membranes exhibit significant ion exclusion at low salt concentration. Our results support a rejection mechanism dominated by electrostatic interactions between fixed membrane charges and mobile ions, while steric and hydrodynamic effects appear to be less important. Comparison with commercial nanofiltration membranes for water softening reveals that our carbon nanotube membranes provides far superior water fluxes for similar ion rejection capabilities.

  4. Solution deposition of thin carbon coatings on LiFePO₄.

    PubMed

    Zhu, Jianxin; Yoo, Kevin; El-Halees, Ibrahim; Kisailus, David

    2014-12-10

    We report the synthesis of ultrathin carbon coatings on polycrystalline LiFePO4 via solution deposition and subsequent annealing. The annealing temperature was systematically investigated with polymer systems on LiFePO4 nanostructures. The crystal structures, sizes, and morphologies were monitored and analyzed by X-ray diffraction (XRD) and scanning electron microscopy (SEM). Micro-Raman and TEM were used to interrogate the carbon coatings after heat-treatments. Electrochemical performance of coated materials was investigated by cyclic voltammograms (CVs) and galvanostatic charge-discharge analysis. The olivine structured LiFePO4 remained stable up to 600 °C but underwent a rapid reduction reaction from LiFePO4 to Fe2P above 700 °C. The good compatibility between polyethylene glycol (PEG) and the surface of LiFePO4 enabled the formation of core-shell structure, which was transformed into a thin carbon coating on LiFePO4 after annealing. Both PEG and sucrose carbon-based sources yielded high-quality carbon coatings after annealing, as determined by the graphitic/disordered (G/D) ratios of 1.30 and 1.20, respectively. By producing more uniform and coherent coatings on LiFePO4 particles, batteries with significantly less carbon (i.e., 0.41 wt %) were fabricated and demonstrated comparable performance to traditionally synthesized carbon-coated LiFePO4 with higher carbon loadings (ca. 2.64 wt %). This will enable development of batteries with higher active material loading and therefore significantly larger energy densities. PMID:25387242

  5. Competitive adsorption of ibuprofen and amoxicillin mixtures from aqueous solution on activated carbons.

    PubMed

    Mansouri, Hayet; Carmona, Rocio J; Gomis-Berenguer, Alicia; Souissi-Najar, Souad; Ouederni, Abdelmottaleb; Ania, Conchi O

    2015-07-01

    This work investigates the competitive adsorption under dynamic and equilibrium conditions of ibuprofen (IBU) and amoxicillin (AMX), two widely consumed pharmaceuticals, on nanoporous carbons of different characteristics. Batch adsorption experiments of pure components in water and their binary mixtures were carried out to measure both adsorption equilibrium and kinetics, and dynamic tests were performed to validate the simultaneous removal of the mixtures in breakthrough experiments. The equilibrium adsorption capacities evaluated from pure component solutions were higher than those measured in dynamic conditions, and were found to depend on the porous features of the adsorbent and the nature of the specific/dispersive interactions that are controlled by the solution pH, density of surface change on the carbon and ionization of the pollutant. A marked roll-up effect was observed for AMX retention on the hydrophobic carbons, not seen for the functionalized adsorbent likely due to the lower affinity of amoxicillin towards the carbon adsorbent. Dynamic adsorption of binary mixtures from wastewater of high salinity and alkalinity showed a slight increase in IBU uptake and a reduced adsorption of AMX, demonstrating the feasibility of the simultaneous removal of both compounds from complex water matrices. PMID:25554087

  6. Removal of organic contaminants from aqueous solution by cattle manure compost (CMC) derived activated carbons

    NASA Astrophysics Data System (ADS)

    Qian, Qingrong; Chen, Qinghua; Machida, Motoi; Tatsumoto, Hideki; Mochidzuki, Kazuhiro; Sakoda, Akiyoshi

    2009-04-01

    The activated carbons (ACs) prepared from cattle manure compost (CMC) with various pore structure and surface chemistry were used to remove phenol and methylene blue (MB) from aqueous solutions. The adsorption equilibrium and kinetics of two organic contaminants onto the ACs were investigated and the schematic models for the adsorptive processes were proposed. The result shows that the removal of functional groups from ACs surface leads to decreasing both rate constants for phenol and MB adsorption. It also causes the decrement of MB adsorption capacity. However, the decrease of surface functional groups was found to result in the increase of phenol adsorption capacity. In our schematic model for adsorptive processes, the presence of acidic functional groups on the surface of carbon is assumed to act as channels for diffusion of adsorbate molecules onto small pores, therefore, promotes the adsorption rate of both phenol and MB. In phenol solution, water molecules firstly adsorb on surface oxygen groups by H-bonding and subsequently form water clusters, which cause partial blockage of the micropores, deduce electrons from the π-electron system of the carbon basal planes, hence, impede or prevent phenol adsorption. On the contrary, in MB solution, the oxygen groups prefer to combine with MB + cations than water molecules, which lead to the increase of MB adsorption capacity.

  7. Adsorption of bisphenol-A from aqueous solution onto minerals and carbon adsorbents.

    PubMed

    Tsai, Wen-Tien; Lai, Chi-Wei; Su, Ting-Yi

    2006-06-30

    The adsorption behaviors of bisphenol-A, which has been listed as one of endocrine disrupting chemicals, from aqueous solution onto four minerals including andesite, diatomaceous earth, titanium dioxide, and activated bleaching earth, and two activated carbons with coconut-based and coal-based virgins were examined in this work. Based on the adsorption results at the specified conditions, the adsorption capacities of activated carbons are significantly larger than those of mineral adsorbents, implying that the former is effective for removal of the highly hydrophobic adsorbate from the aqueous solution because of its high surface area and low surface polarity. The adsorption capacities of bisphenol-A onto these mineral adsorbents with different pore properties are almost similar in magnitude mainly due to the weakly electrostatic interaction between the mineral surface with negative charge and the target adsorbate with hydrophobic nature. Further, a simplified kinetic model, pseudo-second-order, was tested to investigate the adsorption behaviors of bisphenol-A onto the two common activated carbons at different solution conditions. It was found that the adsorption process could be well described with the pseudo-second-order model. The kinetic parameters of the model obtained in the present work are in line with the pore properties of the two adsorbents. PMID:16343748

  8. Optimization of mesoporous carbons for efficient adsorption of berberine hydrochloride from aqueous solutions.

    PubMed

    Li, Yin; Fu, Jie; Deng, Shuguang; Lu, Xiuyang

    2014-06-15

    Sixteen mesoporous carbon adsorbents were synthesized by varying the ratio of soft to hard templates in order to optimize the pore textural properties of these adsorbents. The mesoporous carbon adsorbents have a high BET specific surface area (1590.3-2193.5 m(2)/g), large pore volume (1.72-2.56 cm(3)/g), and uniform pore size distribution with a median pore diameter ranging from 3.51 nm to 4.52 nm. It was observed that pore textural properties of the carbon adsorbents critically depend on the molar ratio of carbon sources to templates, and the hard template plays a more important role than the soft template in manipulating the pore textures. Adsorption isotherms of berberine hydrochloride at 303 K were measured to evaluate the adsorption efficacy of these adsorbents. The adsorption of berberine hydrochloride from aqueous solutions on the sixteen mesoporous carbon adsorbents synthesized in this work is very efficient, and the adsorption equilibrium capacities on all samples are more than double the adsorption capacities of berberine hydrochloride of the benchmark adsorbents (polymer resins and spherical activated carbons) at similar conditions. It was observed from the adsorption experiments that the equilibrium adsorption amounts of berberine hydrochloride are strongly correlated with the BET specific surface area and pore volume of the adsorbents. The adsorbent with the highest BET of 2193.5 m(2)/g displayed the largest adsorption capacity of 574 mg/g at an equilibrium concentration of 0.10mg/mL of berberine hydrochloride in an aqueous solution. PMID:24767505

  9. Photocatalytic reduction of Cr(VI) in aqueous solution using TiO₂ nanoparticles prepared with various alcohols as solvent.

    PubMed

    Ku, Young; Lin, Chia-Nan; Hou, Wei-Ming

    2012-01-01

    TiO₂ nanoparticles were prepared with various linear alkyl chains of alcohols under a sol-gel process. The structure characterization and the photocatalytic reduction of hexavalent chromium of the TiO₂ nanoparticles were investigated. The phase transformation temperature, crystal aggregation and surface area of prepared TiO₂ samples were found to be strongly influenced by alcohol used. The phase transformation from anatase to rutile was retarded and the surface area was reduced for TiO₂ prepared with alcohols of longer alkyl chain. TiO₂ nanoparticles prepared with methanol or ethanol exhibited higher photocatalytic reduction activity of hexavalent chromium possibly due to greater and more positively charged surface area. PMID:22828314

  10. Numerical investigation on the structural characteristics of multiple RBCs in a stenotic microcapillary under plasma-alcohol solution

    NASA Astrophysics Data System (ADS)

    Ni, Aleksey; Cheema, Taqi Ahmad; Park, Cheol Woo

    2015-05-01

    Alcohol significantly affects blood rheology and influences the mechanical behavior of red blood cells (RBCs). Previous studies indicate that plasma-RBC and multiple RBC interaction are important indicators for atherosclerosis progression. Therefore, multiphysics interactions under highly viscous conditions of alcohol consumption and stenosis structure must be investigated. A 2D microcapillary model, wherein multiple RBCs float through a stenotic structure, was established to investigate the effect of alcohol on cell motion and deformability under various flow conditions. Results show that the deformed cells inside the stenosis increase flow resistance and increase plasma velocity gradient in the pre and post stenotic regions. Moreover, the effect of the initial RBC position is important describing the RBC deformation pattern. The structural properties of RBCs may be significantly affected when the stenosis path is filled by cells that increase flow resistance.

  11. Complex formation equilibria of some beta-amino-alcohols with lead(II) and cadmium(II) in aqueous solution.

    PubMed

    Canepari, S; Carunchio, V; Castellano, P; Messina, A

    1998-12-01

    A study of complex formation equilibria of some beta-amino-alcohols with lead(II) and cadmium(II) ions at 25 degrees C and in 0.5 M KNO(3) is reported. The amino-alcohols considered are 2-amino-1-propanol, 2-amino-1-butanol, 2-amino-1-pentanol and 2-amino-1,3-propanediol. sec-Buthylamine and 2-amino-1-methoxy-propane have been also considered for comparison. The results are discussed in terms of ligand structure, paying attention to the number of hydroxyl groups and to the length of the alkyl residual. A weak contribution of the alcoholic oxygen in the coordination of cadmium(II) and the presence of a mixed hydroxyl species in lead(II) containing systems are hypothesized. PMID:18967412

  12. Transport of ions in mesoporous carbon electrodes during capacitive deionization of high-salinity solutions.

    PubMed

    Sharma, K; Kim, Y-H; Gabitto, J; Mayes, R T; Yiacoumi, S; Bilheux, H Z; Walker, L M H; Dai, S; Tsouris, C

    2015-01-27

    Desalination of high-salinity solutions has been studied using a novel experimental technique and a theoretical model. Neutron imaging has been employed to visualize lithium ions in mesoporous carbon materials, which are used as electrodes in capacitive deionization (CDI) for water desalination. Experiments were conducted with a flow-through CDI cell designed for neutron imaging and with lithium-6 chloride ((6)LiCl) as the electrolyte. Sequences of neutron images have been obtained at a relatively high concentration of (6)LiCl solution to provide information on the transport of ions within the electrodes. A new model that computes the individual ionic concentration profiles inside mesoporous carbon electrodes has been used to simulate the CDI process. Modifications have also been introduced into the simulation model to calculate results at high electrolyte concentrations. Experimental data and simulation results provide insight into why CDI is not effective for desalination of high ionic-strength solutions. The combination of experimental information, obtained through neutron imaging, with the theoretical model will help in the design of CDI devices, which can improve the process for high ionic-strength solutions. PMID:25533167

  13. Removal of copper and cadmium from aqueous solution using switchgrass biochar produced via hydrothermal carbonization process.

    PubMed

    Regmi, Pusker; Garcia Moscoso, Jose Luis; Kumar, Sandeep; Cao, Xiaoyan; Mao, Jingdong; Schafran, Gary

    2012-10-30

    Biochar produced from switchgrass via hydrothermal carbonization (HTC) was used as a sorbent for the removal of copper and cadmium from aqueous solution. The cold activation process using KOH at room temperature was developed to enhance the porous structure and sorption properties of the HTC biochar. The sorption efficiency of HTC biochar and alkali activated HTC biochar (HTCB) for removing copper and cadmium from aqueous solution were compared with commercially available powdered activated carbon (PAC). The present batch adsorption study describes the effects of solution pH, biochar dose, and contact time on copper and cadmium removal efficiency from single metal ion aqueous solutions. The activated HTCB exhibited a higher adsorption potential for copper and cadmium than HTC biochar and PAC. Experiments conducted with an initial metal concentration of 40 mg/L at pH 5.0 and contact time of 24 h resulted in close to 100% copper and cadmium removal by activated HTCB at 2 g/L, far greater than what was observed for HTC biochar (16% and 5.6%) and PAC (4% and 7.7%). The adsorption capacities of activated HTCB for cadmium removal were 34 mg/g (0.313 mmol/g) and copper removal was 31 mg/g (0.503 mmol/g). PMID:22687632

  14. Solid / solution interaction: The effect of carbonate alkalinity on adsorbed thorium

    NASA Astrophysics Data System (ADS)

    LaFlamme, Brian D.; Murray, James W.

    1987-02-01

    Elevated activities of dissolved Th have been found in Soap Lake, an alkaline lake in Eastern Washington. Dissolved 232Th ranges from less than 0.001 to 4.9 dpm/L compared to about 1.3 × 10 -5 dpm/ L in sea water. The enhanced activity in the lake coincides with an increase in carbonate alkalinity. Experiments were conducted to evaluate the effect of pH, ionic strength and carbonate alkalinity on Th adsorption on goethite. Thorium (10 -13 M total) in the presence of 5.22 mg/L α-FeOOH and 0.1 M NaNO 3 has an adsorption edge from pH 2-5. At pH 9.0 ± 0.6 the percent Th absorbed on the solid began to decrease from 100% at 100 meq/L carbonate alkalinity and exhibited no adsorption above 300 meq/L. The experimental data were modeled to obtain the intrinsic adsorption equilibrium constants for Th hydrolysis species. These adsorption constants were incorporated in the model to interpret the observed effect of carbonate alkalinity on Th adsorption. There are two main effects of the alkalinity. To a significant degree the decrease in Th adsorption is due to competition of HCO -3 and CO 2-3 ions for surface sites. Dissolved Th carbonate complexes also contribute to the increase of Th in solution.

  15. Picosecond Pulse Radiolysis of Propylene Carbonate as a Solute in Water and as a Solvent.

    PubMed

    Marignier, Jean-Louis; Torche, Fayçal; Le Caër, Sophie; Mostafavi, Mehran; Belloni, Jacqueline

    2016-03-10

    The ester propylene carbonate (PC) is a solvent with a high static dielectric constant where the charges generated by ionizing radiation are expected to be long-lived at room temperature. Time-resolved optical absorption spectroscopy after picosecond electron pulses reveals the formation of a UV band, within less than two nanoseconds, that is assigned to the radical anion PC(-•), arising from a fast attachment reaction of electrons onto PC. Assignment and reactivity of PC(-•) in neat solvent and solutions are discussed in relation with data obtained in solutions of PC in water under reducing or oxidizing conditions and in solutions in PC of aromatic scavengers with various reduction potentials. The fate of the electrons and the ionization yield in PC are compared with those of other solvents. PMID:26840402

  16. Alcohol Alert

    MedlinePlus

    ... main content National Institute on Alcohol Abuse and Alcoholism (NIAAA) Main Menu Search Search form Search Alcohol & ... on a single aspect of alcohol abuse and alcoholism. Please click on the desired publication for full ...

  17. Carbon and Hydrogen Isotope Measurements of Alcohols and Organic Acids by Online Pyroprobe-GC-IRMS

    NASA Technical Reports Server (NTRS)

    Socki, Richard A.; Fu, Qi; Niles, Paul B.; Gibson, Everett K., Jr.

    2012-01-01

    The detection of methane in the atmosphere of Mars, combined with evidence showing widespread water-rock interaction during martian history, suggests that the production of methane on Mars may be the result of mineral surface-catalyzed CO2 and or CO reduction during Fisher-Tropsch Type (FTT) reactions. A better understanding of these reaction pathways and corresponding C and H isotope fractionations is critical to deciphering the synthesis of organic compounds produced under abiotic hydrothermal conditions. Described here is a technique for the extraction and analysis of both C and H isotopes from alcohols (C1-C4) and organic acids (C1-C6). This work is meant to provide a "proof of concept" for making meaningful isotope measurements on complex mixtures of solid-phase hydrocarbons and other intermediary products produced during high-temperature and high-pressure synthesis on mineral-catalyzed surfaces. These analyses are conducted entirely "on-line" utilizing a CDS model 5000 Pyroprobe connected to a Thermo Trace GC Ultra that is interfaced with a Thermo MAT 253 isotope ratio mass spectrometer operating in continuous flow mode. Also, this technique is designed to carry a split of the GC-separated product to a DSQ II quadrupole mass spectrometer as a means of making semi-quantitative compositional measurements. Therefore, both chemical and isotopic measurements can be carried out on the same sample.

  18. Fabrication of carbon nanotube high-frequency nanoelectronic biosensor for sensing in high ionic strength solutions.

    PubMed

    Kulkarni, Girish S; Zhong, Zhaohui

    2013-01-01

    The unique electronic properties and high surface-to-volume ratios of single-walled carbon nanotubes (SWNT) and semiconductor nanowires (NW) make them good candidates for high sensitivity biosensors. When a charged molecule binds to such a sensor surface, it alters the carrier density in the sensor, resulting in changes in its DC conductance. However, in an ionic solution a charged surface also attracts counter-ions from the solution, forming an electrical double layer (EDL). This EDL effectively screens off the charge, and in physiologically relevant conditions ~100 millimolar (mM), the characteristic charge screening length (Debye length) is less than a nanometer (nm). Thus, in high ionic strength solutions, charge based (DC) detection is fundamentally impeded. We overcome charge screening effects by detecting molecular dipoles rather than charges at high frequency, by operating carbon nanotube field effect transistors as high frequency mixers. At high frequencies, the AC drive force can no longer overcome the solution drag and the ions in solution do not have sufficient time to form the EDL. Further, frequency mixing technique allows us to operate at frequencies high enough to overcome ionic screening, and yet detect the sensing signals at lower frequencies. Also, the high transconductance of SWNT transistors provides an internal gain for the sensing signal, which obviates the need for external signal amplifier. Here, we describe the protocol to (a) fabricate SWNT transistors, (b) functionalize biomolecules to the nanotube, (c) design and stamp a poly-dimethylsiloxane (PDMS) micro-fluidic chamber onto the device, and (d) carry out high frequency sensing in different ionic strength solutions. PMID:23912795

  19. Fabrication of Carbon Nanotube High-Frequency Nanoelectronic Biosensor for Sensing in High Ionic Strength Solutions

    PubMed Central

    Kulkarni, Girish S.; Zhong, Zhaohui

    2013-01-01

    The unique electronic properties and high surface-to-volume ratios of single-walled carbon nanotubes (SWNT) and semiconductor nanowires (NW) 1-4 make them good candidates for high sensitivity biosensors. When a charged molecule binds to such a sensor surface, it alters the carrier density5 in the sensor, resulting in changes in its DC conductance. However, in an ionic solution a charged surface also attracts counter-ions from the solution, forming an electrical double layer (EDL). This EDL effectively screens off the charge, and in physiologically relevant conditions ~100 millimolar (mM), the characteristic charge screening length (Debye length) is less than a nanometer (nm). Thus, in high ionic strength solutions, charge based (DC) detection is fundamentally impeded6-8. We overcome charge screening effects by detecting molecular dipoles rather than charges at high frequency, by operating carbon nanotube field effect transistors as high frequency mixers9-11. At high frequencies, the AC drive force can no longer overcome the solution drag and the ions in solution do not have sufficient time to form the EDL. Further, frequency mixing technique allows us to operate at frequencies high enough to overcome ionic screening, and yet detect the sensing signals at lower frequencies11-12. Also, the high transconductance of SWNT transistors provides an internal gain for the sensing signal, which obviates the need for external signal amplifier. Here, we describe the protocol to (a) fabricate SWNT transistors, (b) functionalize biomolecules to the nanotube13, (c) design and stamp a poly-dimethylsiloxane (PDMS) micro-fluidic chamber14 onto the device, and (d) carry out high frequency sensing in different ionic strength solutions11. PMID:23912795

  20. Gas-liquid solubilities of carbon monoxide, carbon dioxide, hydrogen, water, 1-alcohols (1 [<=] n [<=] 6), and n-paraffins (2 [<=] n [<=] 6) in hexadecane, octacosane, 1-hexadecanol, phenanthrene, and tetraethylene glycol at pressures up to 5. 5 MPa and temperatures from 293 to 553 K

    SciTech Connect

    Breman, B.B.; Beenackers, A.A.C.M.; Rietjens, E.W.J.; Stege, R.J.H. . Dept. of Chemical Engineering)

    1994-10-01

    At temperatures between 473 and 673 K and pressures between 2 and 10 MPa, synthesis gas can be converted toward methanol, fuel-methanol (a mixture of methanol and higher alcohols), or a mixture of hydrocarbons (Fischer-Tropsch synthesis), depending on the type of heterogeneous catalyst applied. The gas-liquid solubilities of the solutes carbon monoxide, carbon dioxide, hydrogen, water, ethane, propane, pentane, hexane, methanol, ethanol, 1-propanol, 1-butanol, 1-pentanol, and 1-hexanol in the solvents tetraethylene glycol, hexadecane, octacosane, 1-hexadecanol, and phenanthrene were measured as a function of temperature. The solutes are all reactants or products relevant for synthesis gas conversion into alcohols and/or hydrocarbons. The solvents are seen as potentially attractive for synthesis gas conversion via gas-slurry processes. Experimental conditions varied between 293 and 553 K and 0.06 and 5.5 MPa, covering typical process conditions for synthesis gas conversion. The total set of experimental results consists of 1,533 gas-liquid solubilities divided over 60 binary systems. As far as the authors know hardly any of the gas-liquid solubilities from this set have been reported previously in the literature. Where literature data are available, a comparison is made with their data. This comparison always shows an agreement within the calculated experimental errors with an average deviation of 7.6% and a maximal deviation of 15.0%.

  1. Curing of Furfuryl Alcohol-Impregnated Parts

    NASA Technical Reports Server (NTRS)

    Lawton, J. W.; Brayden, T. H.

    1983-01-01

    Delamination problem in reinforced carbon/carbon parts impregnated with oxalic acid-catalyzed furfuryl alcohol overcome by instituting two additional quality-control tests on alcohol and by changing curing conditions.

  2. The relationship between the adhesion work, the wettability and composition of the surface layer in the systems polymer/aqueous solution of anionic surfactants and alcohol mixtures

    NASA Astrophysics Data System (ADS)

    Zdziennicka, Anna; Jańczuk, Bronisław

    2010-11-01

    Measurements of advancing contact angle ( θ) were carried out on polytetrafluoroethylene (PTFE) and polymethylmethacrylate (PMMA) for aqueous solution of sodium dodecyl sulfate (SDDS) mixtures with methanol, ethanol and propanol in the range of SDDS concentration from 10 -5 to 10 -2 M, and for sodium hexadecyl sulfonate (SHS) with the same alcohols at the SHS concentration ranging from 10 -5 to 8 × 10 -4 M at 293 K. The concentration of methanol, ethanol and propanol used for measurements varied from 0 to 21.1, 11.97 and 6.67 M, respectively. On the basis of the contact angles the critical surface tension of PTFE and PMMA wetting was determined by using for this purpose the relationship between the adhesion and the surface tension and cos θ and surface tension both at constant alcohol and surfactant concentration, respectively. The obtained contact angles were also used in the Young Dupre' equation for calculations of the adhesion work of aqueous solution of mixtures of anionic surfactants and short chain alcohols to PTFE and PMMA surface. The adhesion work calculated in this way was compared to that of the particular components of aqueous solution to these surfaces determined on the basis of the surface tension components and parameters of the surface tension of the surface active agents, water, PTFE and PMMA from van Oss et al. equation. The calculated adhesion work was discussed in the light of the concentration of surface active agents at polymer-water and water-air interface determined from Lucassen-Reynders, Gibbs and Guggenheim-Adam equations.

  3. Precipitation of Co(2+) carbonates from aqueous solution: insights on the amorphous to crystalline transformation.

    NASA Astrophysics Data System (ADS)

    González-López, Jorge; Fernández-González, Ángeles; Jiménez, Amalia

    2016-04-01

    Cobalt is toxic metal that is present only as a trace in the Earth crust. However, Co might concentrate on specific areas due to both natural and anthropogenic factors and thus, soils and groundwater can be contaminated. It is from this perspective that we are interested in the precipitation of cobalt carbonates, since co-precipitation with minerals phases is a well-known method for metal immobilization in the environment. In particular, the carbonates are widely used due to its reactivity and natural abundance. In order to evaluate the cobalt carbonate precipitation at room temperature, a simple experimental work was carried out in this work. The precipitation occurred via reaction of two common salts: 0.05M of CoCl2 and 0.05M of Na2CO3 in aqueous solution. After reaction, the precipitated solid was kept in the remaining water at 25 oC and under constant stirring for different aging times of 5 min, 1 and 5 hours, 1, 2, 4, 7, 30 and 60 days. In addition to the aging and precipitation experiments, we carried out experiments to determine the solubility of the solids. In these experiments each precipitate was dissolved in Milli-Q water until equilibrium was reached and then the aqueous solution was analyzed regarding Co2+ and total alkalinity. Furthermore, acid solution calorimetry of the products were attained. Finally, we modeled the results using the PHREEQC code. Solid and aqueous phase identification and characterization have been extensively reported in a previous work (González-López et al., 2015). The main results of our investigation were the initial precipitation of an amorphous cobalt carbonate that evolve towards a poorly crystalline cobalt hydroxide carbonate with aging treatment. Solubility of both phases have been calculated under two different approaches: precipitation and dissolution. Values of solubility from each approach were obtained with a general error due to differences in experiment conditions, for instance, ionic strength, temperature and

  4. Alcoholism, Alcohol, and Drugs

    ERIC Educational Resources Information Center

    Rubin, Emanuel; Lieber, Charles S.

    1971-01-01

    Describes research on synergistic effects of alcohol and other drugs, particularly barbiturates. Proposes biochemical mechanisms to explain alcoholics' tolerance of other drugs when sober, and increased sensitivity when drunk. (AL)

  5. Bond dissociation mechanism of ethanol during carbon nanotube synthesis via alcohol catalytic CVD technique: Ab initio molecular dynamics simulation

    NASA Astrophysics Data System (ADS)

    Oguri, Tomoya; Shimamura, Kohei; Shibuta, Yasushi; Shimojo, Fuyuki; Yamaguchi, Shu

    2014-03-01

    Dissociation of ethanol on a nickel cluster is investigated by ab initio molecular dynamics simulation to reveal the bond dissociation mechanism of carbon source molecules during carbon nanotube synthesis. C-C bonds in only CHxCO fragments are dissociated on the nickel cluster, whereas there is no preferential structure among the fragments for C-O bond dissociation. The dissociation preference is uncorrelated with the bond dissociation energy of corresponding bonds in freestanding molecules but is correlated with the energy difference between fragment molecules before and after dissociation on the nickel surface. Moreover, carbon-chain formation occurs after C-C bond dissociation in a continuous simulation. What determines the chirality of CNTs? What happens at the dissociation stage of carbon source molecules? Regarding the former question, many researchers have pointed out the good epitaxial relationship between a graphite network and a close-packed facet (i.e., fcc(1 1 1) or hcp(0 0 0 1)) of transition metals [17-19]. Therefore, the correlation between the chirality of CNTs and the angle of the step edge on metal (or metal carbide) surfaces has been closely investigated [20-22]. In association with this geometric matching, the epitaxial growth of graphene on Cu(1 1 1) and Ni(1 1 1) surfaces has recently been achieved via CCVD technique [23-25], which is a promising technique for the synthesis of large-area and monolayer graphene.Regarding the latter question, it is empirically known that the yield and quality of CNT products strongly depend on the choice of carbon source molecules and additives. For example, it is well known that the use of ethanol as carbon source molecules yields a large amount of SWNTs without amorphous carbons (called the alcohol CCVD (ACCVD) technique) compared with the CCVD process using hydrocarbons [4]. Moreover, the addition of a small amount of water dramatically enhances the activity and lifetime of the catalytic metal (called the

  6. Lead and copper removal from aqueous solutions using carbon foam derived from phenol resin.

    PubMed

    Lee, Chang-Gu; Jeon, Jun-Woo; Hwang, Min-Jin; Ahn, Kyu-Hong; Park, Chanhyuk; Choi, Jae-Woo; Lee, Sang-Hyup

    2015-07-01

    Phenolic resin-based carbon foam was prepared as an adsorbent for removing heavy metals from aqueous solutions. The surface of the produced carbon foam had a well-developed open cell structure and the specific surface area according to the BET model was 458.59m(2)g(-1). Batch experiments showed that removal ratio increased in the order of copper (19.83%), zinc (34.35%), cadmium (59.82%), and lead (73.99%) in mixed solutions with the same initial concentration (50mgL(-1)). The results indicated that the Sips isotherm model was the most suitable for describing the experimental data of lead and copper. The maximum adsorption capacity of lead and copper determined to Sips model were 491mgg(-1) and 247mgg(-1). The obtained pore diffusion coefficients for lead and copper were found to be 1.02×10(-6) and 2.42×10(-7)m(2)s(-1), respectively. Post-sorption characteristics indicated that surface precipitation was the primary mechanism of lead and copper removal by the carbon foam, while the functional groups on the surface of the foam did not affect metal adsorption. PMID:25819762

  7. Preconcentration of f-elements from aqueous solution utilizing a modified carbon paste electrode.

    PubMed

    Schumacher, Paul D; Fitzgerald, Kelly A; Schenk, James O; Clark, Sue B

    2011-02-15

    An evaluation using paraffin oil based, Acheson 38 carbon paste electrodes modified with α-hydroxyisobutyric acid (HIBA) to preconcentrate f-elements cathodically is described. The modified paste was made by directly mixing solid HIBA into the carbon paste. A chemically reversible cyclic voltammogram for HIBA was observed on this modified carbon paste, which was found to be a non-Nerstian, single electron transfer process. Lanthanides (less promethium) were found to accumulate onto the electrode surface during a 30 s electrodeposition step at -0.4 V vs Ag/AgCl from 0.1 M LiCl. The elements were then stripped off into a 2% HNO(3) solution by an oxidative step at +0.8 V vs Ag/AgCl; quantitative removal from the electrode was confirmed by ICPMS. Ultratrace solutions with initial concentrations down to 5 parts per quadrillion (ppq) were preconcentrated in 5 min above our instrumental limit of detection (LOD) of around 1 ppt for lanthanides. PMID:21271692

  8. Handwashing compliance in a French university hospital: new perspective with the introduction of hand-rubbing with a waterless alcohol-based solution.

    PubMed

    Girou, E; Oppein, F

    2001-08-01

    The baseline compliance with handwashing in a French university hospital was as low as the compliance rates reported in other countries, i.e., less than 50%. By introducing the use of hand-rubbing with an alcoholic solution, as a substitution method for both handwashing with soap and handwashing with an antiseptic agent, we significantly improved hand-cleansing compliance. Despite these encouraging results, mainly due to the accessibility of these non-aqueous products, three major obstacles remain before a wide acceptance by healthcare workers: distrust in terms of efficacy, distrust in terms of skin tolerance and lack of knowledge on hand-cleansing indications. PMID:11759028

  9. Synthesis of nitrogen-containing carbon by solution plasma in aniline with high-repetition frequency discharges

    NASA Astrophysics Data System (ADS)

    Hyun, Koangyong; Ueno, Tomonaga; Saito, Nagahiro

    2016-01-01

    Nitrogen-containing carbon nanoparticles were synthesized in aniline by solution plasma with high-repetition frequency discharges. We developed a bipolar pulsed power supply that can apply high-repetition frequencies ranging from 25 to 200 kHz. By utilizing high-repetition frequencies, conductive carbons were directly synthesized. The crystallinity was increased and H/C ratio of carbon was decreased. Furthermore, nitrogen atoms were simultaneously embedded in the carbon matrix. Due to the presence of nitrogen atoms, the conductivity and electrocatalytic activity of the samples were remarkably improved compared to that of a pure carbon matrix synthesized from a benzene precursor.

  10. Conversion of a metal-organic framework to N-doped porous carbon incorporating Co and CoO nanoparticles: direct oxidation of alcohols to esters.

    PubMed

    Zhou, Yu-Xiao; Chen, Yu-Zhen; Cao, Lina; Lu, Junling; Jiang, Hai-Long

    2015-05-14

    A Co-based metal-organic framework, ZIF-67, has been exploited as a self-template to afford N-doped porous carbon incorporating Co NPs with surface-oxidized CoO species, which exhibit excellent catalytic activity, selectivity and magnetic recyclability toward the direct oxidation of alcohols to esters with O2 as a benign oxidant under mild conditions. PMID:25877956

  11. High-Strength Single-Walled Carbon Nanotube/Permalloy Nanoparticle/Poly(vinyl alcohol) Multifunctional Nanocomposite Fiber.

    PubMed

    Zhou, Gengheng; Wang, Yi-Qi; Byun, Joon-Hyung; Yi, Jin-Woo; Yoon, Sang-Su; Cha, Hwa-Jin; Lee, Jea-Uk; Oh, Youngseok; Jung, Byung-Mun; Moon, Ho-Jun; Chou, Tsu-Wei

    2015-11-24

    Magnetic nanocomposite fibers are a topic of intense research due to their potential breakthrough applications such as smart magnetic-field-response devices and electromagnetic interference (EMI) shielding. However, clustering of nanoparticles in a polymer matrix is a recognized challenge for obtaining a property-controllable nanocomposite fiber. Another challenge is that the strength and ductility of the nanocomposite fiber decrease significantly with increased weight loading of magnetic nanoparticles in the fiber. Here, we report high-strength single-walled carbon nanotube (SWNT)/permalloy nanoparticle (PNP)/poly(vinyl alcohol) multifunctional nanocomposite fibers fabricated by wet spinning. The weight loadings of SWNTs and PNPs in the fiber were as high as 12.0 and 38.0%, respectively. The tensile strength of the fiber was as high as 700 MPa, and electrical conductivity reached 96.7 S m(-1). The saturation magnetization (Ms) was as high as 24.8 emu g(-1). The EMI attenuation of a fabric woven from the prepared fiber approached 100% when tested with electromagnetic waves with a frequency higher than 6 GHz. The present study demonstrates that a magnetic-field-response device can be designed using the fabricated multifunctional nanocomposite fiber. PMID:26431310

  12. Sulfur passivation of InSb(1 0 0) surfaces: Comparison of aqueous and alcoholic ammonium sulfide solutions using X-ray photoemission spectroscopy

    NASA Astrophysics Data System (ADS)

    Lvova, Tatiana V.; Shakhmin, Aleksandr L.; Sedova, Irina V.; Lebedev, Mikhail V.

    2014-08-01

    The chemical composition and the electronic properties of the n-InSb(1 0 0) surface treated with ammonium sulfide dissolved in water or in 2-propanol has been studied by X-ray photoemission spectroscopy. The solvent determines the mechanism of chemical reaction between InSb(1 0 0) surface and sulfide solution. The variation of the solvent leads to variations in chemical composition and electronic structure of the final sulfide layers. Aqueous sulfide solution withdraws antimony atoms from the InSb(1 0 0) surface very fast due to solubility of antimony sulfides, whereas after treatment with alcoholic sulfide solution the antimony sulfides remain on the surface. The Fermi level at the InSb(1 0 0)/passivation layer interface occurs usually deeply in the conduction band of semiconductor and its position depends on the time of sulfur treatment. However, after prolonged treatment with aqueous sulfide solution and surface depletion with antimony the Fermi level is found in the valence band. Although both solutions remove the native oxide layer, the residual oxygen content is lower after treatment with the solution of ammonium sulfide in 2-propanol.

  13. Dissolution of Uranium(IV) Oxide in Solutions of Ammonium Carbonate and Hydrogen Peroxide

    SciTech Connect

    Smith, Steven C.; Peper, Shane M.; Douglas, Matthew; Ziegelgruber, Kate L.; Finn, Erin C.

    2009-09-12

    Understanding the dissolution characteristics of uranium oxides is of fundamental scientific interest. Bench scale experiments were conducted to determine the optimal dissolution parameters of uranium(IV) oxide (UO2) powder in solutions of ammonium carbonate [(NH4)2CO3] and hydrogen peroxide (H2O2). Experimental parameters included variable peroxide and carbonate concentrations, and temperature. Results indicate the dissolution rate of UO2 in 1 M (NH4)2CO3 increases linearly with peroxide concentration ranging from 0.05 – 2 M (1:1 to 40:1 mol ratio H2O2:U), with no apparent maximum rate reached under the limited conditions used in our study. Temperature ranging studies show the dissolution rate of UO2 in 1 M (NH4)2CO3 and 0.1 M H2O2 (2:1 mol ratio H2O2:U) increases linearly from 15 °C to 60 °C, again with no apparent maximum rate reached. Dissolution of UO2 in solutions with constant [H2O2] and [(NH4)2CO3] ranging from 0.5 to 2 M showed no difference in rate; however dissolution was significantly reduced in 0.05 M (NH4)2CO3 solution. The results of this study demonstrate the influence of [H2O2], [(NH4)2CO3], and temperature on the dissolution of UO2 in peroxide-containing (NH4)2CO3 solutions. Future studies are planned to elucidate the solution and solid state complexes in these systems.

  14. Effect of solution additives on the performance of PMAN carbon anodes in 1M LiPF{sub 6}/EC-DMC solutions

    SciTech Connect

    Guidotti, R.A.; Johnson, B.J.

    1996-12-31

    A study was undertaken to examine the use of a number of solution additives in 1M LiPF{sub 6}/ethylene carbonate (EC)-dimethyl carbonate (DMC) solutions to improve the performance of carbon anodes derived from polymethylacrylonitrile (PMAN)-divinylbenzene (DVB) copolymers. The study goals were to improve the cycle life and reduce the formation of the passivation layer during the first reduction, thereby minimizing the irreversible-capacity losses. Additives studied were 12-crown-4 (12-Cr-4) ether, decalin, and dilithium phthalocyanine (Li{sub 2}Pc). The carbon performance was characterized by galvanostatic cycling, cyclic voltammetry, and complex-impedance spectroscopy. Limited success was obtained with 12-Cr-4 ether at 0.25 M and decalin at 1 v/o. Poor results were noted with Li{sub 2}Pc at 0.025 M and 0.5 M.

  15. Atomic Force Microscopy of DNA-wrapped Single-walled Carbon Nanotubes in Aqueous Solution.

    PubMed

    Hayashida, Takuya; Umemura, Kazuo

    2016-07-01

    We evaluated hybrids of DNA and single-walled carbon nanotubes (SWNTs) in aqueous solution and in air using atomic force microscopy (AFM). Although intensive AFM observations of these hybrids were previously carried out for samples in air, this is the first report on AFM observations of these hybrids in solution. As expected, diameters of DNA-SWNT hybrids dramatically increased in tris(hydroxymethyl)aminomethane-ethylenediaminetetraacetic acid (TE) buffer solution. The data suggest that DNA molecules maintain their structures even on the SWNT surfaces. Furthermore, we simultaneously observed single DNA-SWNT hybrids using three different AFM modes in air and in the TE buffer solution. Height value of the hybrids was largest in the solution, and lowest for the mode that repulsive force is expected in air. For the bare SWNT molecules, height differences among the three AFM modes were much lower than those of the DNA-SWNT hybrids. DNA molecules adsorbed on SWNT surfaces flexibly changed their morphology as well as DNA molecules on flat surfaces such as mica. This is hopeful results for biological applications of DNA-SWNT hybrids. In addition, our results revealed the importance of the single-molecule approach to evaluate DNA structures on SWNT surfaces. PMID:27045980

  16. Integration of High-Purity Carbon Nanotube Solution into Electronic Devices

    NASA Astrophysics Data System (ADS)

    Tulevski, George; IBM TJ Watson Reserach Center Team

    Due to their exceptional electronic properties, carbon nanotubes (cnt) are leading candidates to be employed as channel materials in future nanoelectronic devices. A key bottleneck to realizing device integration is the sorting of carbon nanotubes, namely the isolation of high-purity, semiconducting cnt solutions. This talk will describe our efforts in using polymer-based sorting methods to isolate high-density and high-purity semiconducting cnt solutions. We explore the dependence of starting material and polymer to cnt ratio on the effectiveness of the separation. We confirm optically and electrically that the semiconducting purity is >99.99% through several thousand individual device measurements. In addition to single-cnt devices, thin-film transistors were also fabricated and tested. Due to the high purity of the solutions, device switching (~105 ION/IOFF) was observed at channel lengths below the percolation threshold (<500 nm). Operating below the percolation threshold allows for devices with much higher current densities and effective mobilities as transport is now the result of direct transport as opposed to hopping between cnts.

  17. Computer Simulation of Cascade Damage in α-Iron with Carbon in Solution

    SciTech Connect

    Andrew, Calder F; Bacon, David J; Barashev, Aleksandr; Osetskiy, Yury N

    2008-01-01

    Molecular dynamics simulation method is used to investigate defect production by displacement cascades in iron with carbon (C) in solution. This is the first study of cascade damage in a metal containing interstitial solute. Iron is of particular interest because of the use of ferritic steels in plant for nuclear power generation. Cascades are simulated with energy in the range 5 to 20keV in iron at either 100 or 600K containing carbon with concentration in the range 0 to 1at%. C in solution has no discernible effect on the number of defects produced in cascades under any of the conditions simulated, nor on the clustered fraction of either self-interstitial atoms (SIAs) or vacancies. However, significant fractions of single SIAs and vacancies are trapped by C in the cascade process, irrespective of cascade energy. The fraction is independent of temperature for vacancies, but increases strongly with temperature for SIAs: this is a consequence of the higher mobility of the SIA.

  18. Solution-processed thin films for electronics from single-walled carbon nanotubes and graphene

    NASA Astrophysics Data System (ADS)

    Eda, Goki

    Single-walled carbon nanotubes (SWNTs) and graphene are sp 2 hybridized carbon nanostructures which exhibit extraordinary electronic properties arising from their unique energy dispersions and dimensionalities. A major issue preventing implementation of these materials into integrated electronic devices is the absence of large-scale controllable synthesis and subsequent manipulation. To circumvent this issue, solution processing of SWNTs and graphene has been proposed. Deposition of thin film networks allows the realization of a new class of materials that are useful for large-area or "macro-electronics" on flexible and inexpensive platforms. In this thesis, controllable and efficient solution-based deposition of SWNT and graphene thin film networks and their opto-electronic properties are investigated. Topics such as material dynamics in liquid, chemical structures, defects, morphology, and doping are studied utilizing various spectroscopy and microscopy analysis along with complementary electrical measurements. Further insight is provided through demonstrations of proof-of-principle thin film transistors, organic photovoltaics, and field emitters based on solution-processed SWNT and graphene thin films.

  19. Role of PF6- in the radiolytical and electrochemical degradation of propylene carbonate solutions

    NASA Astrophysics Data System (ADS)

    Ortiz, Daniel; Jimenez Gordon, Isabel; Legand, Solène; Dauvois, Vincent; Baltaze, Jean-Pierre; Marignier, Jean-Louis; Martin, Jean-Frédéric; Belloni, Jacqueline; Mostafavi, Mehran; Le Caër, Sophie

    2016-09-01

    The behavior under irradiation of neat propylene carbonate (PC), a co-solvent usually used in Li-ion batteries (LIB), and also of Li salt solutions is investigated. The decomposition of neat PC is studied using radiolysis in the pulse and steady state regime and is assigned to the ultrafast formation, in the reducing channel, of the radical anion PCrad - by electron attachment, followed by the ring cleavage, leading to CO. In the oxidative channel, the PC(sbnd H)rad radical is formed, generating CO2. The CO2 and CO yields are both close to the ionization yield of PC. The CO2 and CO productions in LiClO4, LiBF4 and LiN(CF3)2(SO2)2 solutions are similar as in neat PC. In contrast, in LiPF6/PC a strong impact on PC degradation is measured with a doubling of the CO2 yield due to the high reactivity of the electron towards PF6- observed in the picosecond range. A small number of oxide phosphine molecules are detected among the various products of the irradiated solutions, suggesting that most of them, observed in carbonate mixtures used in LIBs, arise from linear rather than from cyclical molecules. The similarity between the degradation by radiolysis or electrolysis highlights the interest of radiolysis as an accelerated aging method.

  20. The Electrochemical Behavior of Zn-Mn Alloy Coating in Carbonated Concrete Solution

    NASA Astrophysics Data System (ADS)

    Touazi, S.; Bučko, M.; Makhloufi, L.; Legat, A.; Bajat, J. B.

    2016-05-01

    In order to improve the protective performance of Zn coating on reinforcing steel in concrete, the electrochemical deposition of Zn-Mn coatings was conducted on steel surface. The morphology, chemical and phase compositions of Zn-Mn coatings obtained from sulfate-citrate bath were investigated in the first part of paper. In the second part, the obtained deposits were tested in solution simulating carbonated concrete, consisting of NaHCO3 and Na2CO3. Data obtained from Tafel analysis showed higher corrosion resistance for Zn-Mn alloy deposits obtained at -1700 and -1800mV versus SCE, when compared to pure Zn deposit. Impedance spectroscopy investigations revealed that the total impedance of Zn-Mn coatings increased steadily with time, and was significantly higher as compared to pure Zn after 24h in corrosion solution. On the contrary, for pure Zn, the impedance increased in the first 12h, and then decreased during prolonged exposure time, which can be explained by rapid growth of nonprotective white rust and the degradation of zinc coating, as was confirmed by optical microscope after 24h of immersion in carbonated concrete pore solution.

  1. Development and distribution of bed-parallel compaction bands and pressure solution seams in carbonates (Bolognano Formation, Majella Mountain, Italy)

    NASA Astrophysics Data System (ADS)

    Rustichelli, A.; Tondi, E.; Agosta, F.; Cilona, A.; Giorgioni, M.

    2012-04-01

    The Oligo-Miocene ramp carbonates pertaining to the Bolognano Formation, cropping out at the Majella Mountain, Central Italy, are diffusely crosscut by bed-parallel structural elements such as compaction bands and pressure solution seams. These bed-parallel structural elements formed under a vertical loading, during the progressive burial of the carbonates. The present field and laboratory study focuses on the control exerted, on development and distribution of bed-parallel compaction bands and pressure solution seams, by compositional, sedimentological and pore network characteristics of a variety of carbonate rocks (skeletal grainstones and packstones, marly wackestones to mudstones). The main results are consistent with the following statements: (i) bed-parallel compaction bands formed only within poorly cemented, porous grainstones (2D porosity > 10%; 3D porosity > 15%). Their dimensional parameters (i.e., length, spacing, thickness) were strongly controlled by both sorting and sphericity of the carbonate grains, as well as by the amount of intergranular macroporosity. All these rock characteristics enhanced all physical processes (i.e. grain rotation, translation and fracturing) associated to compaction banding; (ii) bed-parallel pressure solution seams predominantly formed within fine-grained packstones made up of well-sorted and spherical carbonate grains with absence of internal pores, and small amounts of clayish matrix (2-4% of total rock volume). High contents of pre-existing cement also enhanced pressure solution; (iii) well-sorted carbonates with spherical grains may be suitable to both compaction banding and pressure solution; (iv) skeletal grain types which compose grain-supported carbonate rocks (grainstones and packstones), in many cases, indirectly influence the distribution of both bed-parallel compaction bands and pressure solution seams. Considering that the containment and migration capacity of geofluids in the subsurface within carbonate

  2. ANIONIC EXCHANGE PROCESS FOR THE RECOVERY OF URANIUM AND VANADIUM FROM CARBONATE SOLUTIONS

    DOEpatents

    Bailes, R.H.; Ellis, D.A.; Long, R.S.

    1958-12-16

    Uranium and vanadium can be economically purified and recovered from non- salt roast carbonate leach liquors by adsorption on a strongly basic anionic exchange resin and subsequent selective elution by one of three alternative methods. Method 1 comprises selectively eluting uranium from the resin with an ammonium sulfate solution followed by eluting vanadium from the resin with either 5 M NaCl, saturated (NH/sub 4/)/sub 2/CO/sub 3/, saturated NaHCO/sub 3/, 1 M NaOH, or saturated S0/sub 2/ solutions. Method II comprises selectively eluting vanadium from the resin with either concentrated NaCl or S0/sub 2/ solutions subsequent to pretreatment of the column with either S0/sub 2/ gas, 1 N HCl, or 0.1 N H/sub 2/8O/sub 4/ followed by eluting uranium from the resin with solutions containing 0.9 M NH/sub 4/Cl or NaCl and 0.1 Cl. Method III comprises flowing the carbonate leac solutlon through a first column of a strongly basic anlonlc exchange resin untll vanadium breakthrough occurs, so that the effluent solution is enriched ln uranium content and the vanadium is chiefly retalned by the resln, absorbing the uranlum from the enriched effluent solution on a second column of a strongly basic anionic exchange resin, pretreating the first column with either 0.1 N HCl, 0.1 H/sub 2/SO/sub 4/, C0/sub 2/ gas, or ammonium sulfate, selectively eluting the vanadlum from the column with saturated S0/sub 2/ solution, pretreatlng the second column with either 0.1 N HCl or S0/sub 2/ gas, selectively eluting residual vanadium from the column with saturated S0/sub 2/ solution, and then eluting the uranium from the column with either 0.1 N HCl and 1 N NaCl orO.l N HCl and 1 N NH/sub 4/Cl.

  3. Dynamic effects in the production of diamond from solid-solution carbon

    SciTech Connect

    Sobolev, V.V.; Didyk, R.P.; Merezhko, Y.I.; Skidanenko, A.I.; Slobodskoi, V.Y.

    1984-03-01

    The authors examine the scope for diamond to grow at atmospheric pressure in iron alloys. For the purpose of this investigation, diamond nuclei were produced in a cast-iron specimen by a dynamic pressure of 80-90GPa. The mass proportion of diamond polycrystals of maximum size 40-50 ..mu..m did not exceed 1%. The largest diamond content occurred in the fraction 0.1-5 ..mu..m and constituted about 80%. The studies show that: the presence of diamond inclusions in a metal matrix substantially influences the structural transformations during isothermal heating and slow cooling; the solid-solution carbon, the carbon compounds, and the graphite inclusions can serve as sources of carbon in the growth of diamond crystals in the metastable region; and dynamic pressures generate numerous defects in cast-iron specimens, which are sources of vacancies, which facilitate the diffusion of the carbon to the growing diamond crystals and the removal of iron from them.

  4. A comparison of fenuron degradation by hydroxyl and carbonate radicals in aqueous solution.

    PubMed

    Mazellier, Patrick; Busset, Cécile; Delmont, Anne; De Laat, Joseph

    2007-12-01

    A comparative study of the transformation of the herbicide fenuron (1,1-dimethyl-3-phenylurea) by hydroxyl radicals and carbonate radicals in aqueous solution (pH 7.2-phosphate buffer) has been undertaken. Hydroxyl radical was generated by the well-known photolysis of hydrogen peroxide at 254 nm and carbonate radical was formed by photolysis of Co(NH(3))(5)CO(3)(+) at 254 nm. Competitive kinetic experiments were performed with atrazine used as the main competitor for both processes. Accordingly, the second-order rate constant of reaction between fenuron and carbonate radical was found to be (7-12+/-3)x10(6)M(-1)s(-1) [(7+/-1)x10(9)M(-1)s(-1) for hydroxyl radical]. The formation of degradation products was studied by LC-MS in the two cases and a comparison has been performed. The reaction with carbonate radical leads to the formation of a quinone-imine derivative which appears as the major primary product together with ortho and para hydroxylated compounds. These two compounds represent the major products in the reaction with hydroxyl radicals. The reaction of both radicals also leads to the transformation of the dimethylurea moiety. PMID:17675205

  5. Carbon enters silica forming a cristobalite-type CO2-SiO2 solid solution.

    PubMed

    Santoro, Mario; Gorelli, Federico A; Bini, Roberto; Salamat, Ashkan; Garbarino, Gaston; Levelut, Claire; Cambon, Olivier; Haines, Julien

    2014-01-01

    Extreme conditions permit unique materials to be synthesized and can significantly update our view of the periodic table. In the case of group IV elements, carbon was always considered to be distinct with respect to its heavier homologues in forming oxides. Here we report the synthesis of a crystalline CO2-SiO2 solid solution by reacting carbon dioxide and silica in a laser-heated diamond anvil cell (P = 16-22 GPa, T>4,000 K), showing that carbon enters silica. Remarkably, this material is recovered to ambient conditions. X-ray diffraction shows that the crystal adopts a densely packed α-cristobalite structure (P4(1)2(1)2) with carbon and silicon in fourfold coordination to oxygen at pressures where silica normally adopts a sixfold coordinated rutile-type stishovite structure. An average formula of C0.6(1)Si0.4(1)O2 is consistent with X-ray diffraction and Raman spectroscopy results. These findings may modify our view on oxide chemistry, which is of great interest for materials science, as well as Earth and planetary sciences. PMID:24781844

  6. Carbon enters silica forming a cristobalite-type CO2-SiO2 solid solution

    NASA Astrophysics Data System (ADS)

    Santoro, Mario; Gorelli, Federico A.; Bini, Roberto; Salamat, Ashkan; Garbarino, Gaston; Levelut, Claire; Cambon, Olivier; Haines, Julien

    2014-04-01

    Extreme conditions permit unique materials to be synthesized and can significantly update our view of the periodic table. In the case of group IV elements, carbon was always considered to be distinct with respect to its heavier homologues in forming oxides. Here we report the synthesis of a crystalline CO2-SiO2 solid solution by reacting carbon dioxide and silica in a laser-heated diamond anvil cell (P=16-22 GPa, T>4,000 K), showing that carbon enters silica. Remarkably, this material is recovered to ambient conditions. X-ray diffraction shows that the crystal adopts a densely packed α-cristobalite structure (P41212) with carbon and silicon in fourfold coordination to oxygen at pressures where silica normally adopts a sixfold coordinated rutile-type stishovite structure. An average formula of C0.6(1)Si0.4(1)O2 is consistent with X-ray diffraction and Raman spectroscopy results. These findings may modify our view on oxide chemistry, which is of great interest for materials science, as well as Earth and planetary sciences.

  7. The removal of uranium (VI) from aqueous solutions onto activated carbon developed from grinded used tire.

    PubMed

    Belgacem, Ahmed; Rebiai, Rachid; Hadoun, Hocine; Khemaissia, Sihem; Belmedani, Mohamed

    2014-01-01

    In this study, activated carbon was prepared from waste tire by KOH chemical activation. The pore properties including the BET surface area, pore volume, pore size distribution, and average pore diameter were characterized. BET surface area of the activated carbon was determined as 558 m(2)/g. The adsorption of uranium ions from the aqueous solution using this activated carbon has been investigated. Various physico-chemical parameters such as pH, initial metal ion concentration, and adsorbent dosage level and equilibrium contact time were studied by a batch method. The optimum pH for adsorption was found to be 3. The removal efficiency has also been determined for the adsorption system as a function of initial concentration. The experimental results were fitted to Langmuir, Freundlich, and Dubinin-Radushkevich (D-R) isotherm models. A comparison of best-fitting was performed using the coefficient of correlation and the Langmuir isotherm was found to well represent the measured sorption data. According to the evaluation using the Langmuir equation, the saturated monolayer sorption capacity of uranium ions onto waste tire activated carbon was 158.73 mg/g. The thermodynamic equilibrium constant and the Gibbs free energy were determined and results indicated the spontaneous nature of the adsorption process. Kinetics data were best described by pseudo-second-order model. PMID:23821251

  8. Role of the surface chemistry of activated carbons in dye removal from aqueous solution

    NASA Astrophysics Data System (ADS)

    Zhou, Hua-lei; Zhen, Wen-juan; Zhu, Qian; Wu, Xiao-bin; Chang, Zhi-dong; Li, Wen-jun

    2015-07-01

    Commercial activated carbons were modified by a series of chemical or physical treatments using H2O2, NH3, and heating under N2 flow without notably changing their pore structures. The resultant carbons were characterized by N2 adsorption and Bohem titration and then used to remove Ponceau 4R, methyl orange and brilliant blue from aqueous solutions. Surface chemistry was found to play a significantly different role in removing these three compounds. The removal of anionic Ponceau 4R increases with increasing carbon surface basicity due to the predominant dispersive interaction mechanism. In contrast, surface chemistry has little effect on the removal of anionic methyl orange, which can be explained by two parallel mechanisms involving electrostatic and dispersive interactions due to the basic amine group in a dye molecule. The influence of surface chemistry on the removal of amphoteric brilliant blue dye can also be ignored due to a weak interaction between the carbons and dye molecules, which is resulted from strong cohesive energy from electrostatic forces inside amphoteric dye molecules.

  9. Macromolecular conformation in solution. Study of carbonic anhydrase by the positron annihilation technique.

    PubMed Central

    Handel, E D; Graf, G; Glass, J C

    1980-01-01

    The structural features of carbonic anhydrase (carbonate hydro-lyase; EC 4.2.1.1) in aqueous solution were probed by the positron annihilation technique. The data obtained under varying conditions of temperature, pH, and enzyme concentration were interpreted in terms of the free volume model. The change of enzymic activity with temperature is accompanied by a change in free volume of the protein. Upon thermal denaturation an irreversible change in free volume of the molecule occurred. At low temperatures the protein-water interactions were investigated. These results are discussed in terms of current concepts of structure-function relationships in proteins. This study shows the sensitivity of the positron annihilation method toward the structure of proteins related to their overall conformation and to the nature of bound water. PMID:6789901

  10. Decontamination of adsorbed chemical warfare agents on activated carbon using hydrogen peroxide solutions.

    PubMed

    Osovsky, Ruth; Kaplan, Doron; Nir, Ido; Rotter, Hadar; Elisha, Shmuel; Columbus, Ishay

    2014-09-16

    Mild treatment with hydrogen peroxide solutions (3-30%) efficiently decomposes adsorbed chemical warfare agents (CWAs) on microporous activated carbons used in protective garments and air filters. Better than 95% decomposition of adsorbed sulfur mustard (HD), sarin, and VX was achieved at ambient temperatures within 1-24 h, depending on the H2O2 concentration. HD was oxidized to the nontoxic HD-sulfoxide. The nerve agents were perhydrolyzed to the respective nontoxic methylphosphonic acids. The relative rapidity of the oxidation and perhydrolysis under these conditions is attributed to the microenvironment of the micropores. Apparently, the reactions are favored due to basic sites on the carbon surface. Our findings suggest a potential environmentally friendly route for decontamination of adsorbed CWAs, using H2O2 without the need of cosolvents or activators. PMID:25133545

  11. Dehydration and crystallization of amorphous calcium carbonate in solution and in air

    PubMed Central

    Ihli, Johannes; Wong, Wai Ching; Noel, Elizabeth H.; Kim, Yi-Yeoun; Kulak, Alexander N.; Christenson, Hugo K.; Duer, Melinda J.; Meldrum, Fiona C.

    2014-01-01

    The mechanisms by which amorphous intermediates transform into crystalline materials are poorly understood. Currently, attracting enormous interest is the crystallization of amorphous calcium carbonate, a key intermediary in synthetic, biological and environmental systems. Here we attempt to unify many contrasting and apparently contradictory studies by investigating this process in detail. We show that amorphous calcium carbonate can dehydrate before crystallizing, both in solution and in air, while thermal analyses and solid-state nuclear magnetic resonance measurements reveal that its water is present in distinct environments. Loss of the final water fraction—comprising less than 15% of the total—then triggers crystallization. The high activation energy of this step suggests that it occurs by partial dissolution/recrystallization, mediated by surface water, and the majority of the particle then crystallizes by a solid-state transformation. Such mechanisms are likely to be widespread in solid-state reactions and their characterization will facilitate greater control over these processes. PMID:24469266

  12. Utilization of carbon nanotubes for the removal of rhodamine B dye from aqueous solutions.

    PubMed

    Kumar, Sandeep; Bhanjana, Gaurav; Jangra, Kavita; Dilbaghi, Neeraj; Umar, Ahmad

    2014-06-01

    Carbon nanotubes (CNTs) are attracting increasing research interest as promising adsorbents for harmful cations, anions, and other organic and inorganic impurities present in natural sources of water. This study examined the feasibility of removing Rhodamine B dye from aqueous solutions using multi walled carbon nanotubes (MWCNTs) synthesized by chemical vapor deposition (CVD) method. The effects of dye concentration, pH and contact time on adsorption of direct dye by CNTs were also evaluated. The study used the Langmuir and Temkin isotherms to describe equilibrium adsorption. Additionally, pseudo second-order model was adopted to evaluate experimental data and thereby elucidate the kinetic adsorption process. The adsorption percentage of dye increased as contact time increased. Conversely, the adsorption percentage of dye decreased as dye concentration increased. The pseudo second-order model best represented adsorption kinetics. The capacity of CNTs to adsorb Rhodamine B was 65-90% at different pH values. PMID:24738392

  13. CO2 Absorption in an Alcoholic Solution of Heavily Hindered Alkanolamine: Reaction Mechanism of 2-(tert-Butylamino)ethanol with CO2 Revisited.

    PubMed

    Xie, Hong-Bin; Wei, Xiaoxuan; Wang, Pan; He, Ning; Chen, Jingwen

    2015-06-18

    To advance the optimal design of amines for postcombustion CO2 capture, a sound mechanistic understanding of the chemical process of amines with good CO2 capture performance is advantageous. A sterically hindered alkanolamine, 2-(tert-butylamino)ethanol (TBAE), in ethylene glycol (EG) solution was recently reported to have better CO2 capture performance and unusual reactivity toward CO2, in comparison with those of the prototypical alkanolamines. However, the reaction mechanism of TBAE with CO2 in EG solution is unclear. Here, various quantum chemistry methods were employed to probe the reaction mechanism of TBAE with CO2 in EG and aqueous solution. Six reaction pathways involving three kinds of possible reactive centers of TBAE solution were considered. The results indicated that the formation of anionic hydroxyethyl carbonate by the attack of -OH of EG on CO2 is the most favorable, which is confirmed by complementary high-resolution mass spectrum experiments. This clarified that the speculated zwitterionic carbonate species is not the main product in EG solution. The reaction process of TBAE in aqueous solution is similar to that in EG solution, leading to bicarbonate, which agrees with experimental observations. On the basis of the unveiled reaction mechanisms of TBAE + CO2, the role of the key tert-butyl functional group of TBAE was revealed. PMID:25993508

  14. Adsorption of Reactive Red M-2BE dye from water solutions by multi-walled carbon nanotubes and activated carbon.

    PubMed

    Machado, Fernando M; Bergmann, Carlos P; Fernandes, Thais H M; Lima, Eder C; Royer, Betina; Calvete, Tatiana; Fagan, Solange B

    2011-09-15

    Multi-walled carbon nanotubes and powdered activated carbon were used as adsorbents for the successful removal of Reactive Red M-2BE textile dye from aqueous solutions. The adsorbents were characterised by infrared spectroscopy, N(2) adsorption/desorption isotherms and scanning electron microscopy. The effects of pH, shaking time and temperature on adsorption capacity were studied. In the acidic pH region (pH 2.0), the adsorption of the dye was favourable using both adsorbents. The contact time to obtain equilibrium at 298K was fixed at 1h for both adsorbents. The activation energy of the adsorption process was evaluated from 298 to 323K for both adsorbents. The Avrami fractional-order kinetic model provided the best fit to the experimental data compared with pseudo-first-order or pseudo-second-order kinetic adsorption models. For Reactive Red M-2BE dye, the equilibrium data were best fitted to the Liu isotherm model. Simulated dyehouse effluents were used to check the applicability of the proposed adsorbents for effluent treatment. PMID:21724329

  15. Adsorption of alkenyl succinic anhydride from solutions in carbon tetrachloride on a fine magnetite surface

    NASA Astrophysics Data System (ADS)

    Balmasova, O. V.; Ramazanova, A. G.; Korolev, V. V.

    2016-06-01

    The adsorption of alkenyl succinic anhydride from a solution in carbon tetrachloride on a fine magnetite surface at a temperature of 298.15 K is studied using fine magnetite, which forms the basis of magnetic fluids, as the adsorbent. An adsorption isotherm is recorded and interpreted in terms of the theory of the volume filling of micropores (TVFM). Adsorption process parameters are calculated on the basis of the isotherm. It is shown that at low equilibrium concentrations, the experimental adsorption isotherm is linear in the TVFM equation coordinates.

  16. A Hydro-mechanical Model and Analytical Solutions for Geomechanical Modeling of Carbon Dioxide Geological Sequestration

    SciTech Connect

    Xu, Zhijie; Fang, Yilin; Scheibe, Timothy D.; Bonneville, Alain

    2012-05-15

    We present a hydro-mechanical model for geological sequestration of carbon dioxide. The model considers the poroelastic effects by taking into account the coupling between the geomechanical response and the fluid flow in greater detail. The simplified hydro-mechanical model includes the geomechanical part that relies on the linear elasticity, while the fluid flow is based on the Darcy’s law. Two parts were coupled using the standard linear poroelasticity. Analytical solutions for pressure field were obtained for a typical geological sequestration scenario. The model predicts the temporal and spatial variation of pressure field and effects of permeability and elastic modulus of formation on the fluid pressure distribution.

  17. Carbonized material adsorbents for the removal of mercury from aqueous solutions

    SciTech Connect

    1996-10-01

    Charcoal in itself is porous making it an excellent material for activated charcoal manufacture. However, few studies have been conducted in harnessing its potential for adsorption purposes, especially in water treatment. This paper describes the possibility of utilizing charcoal materials from Sugi (Cryptomeria japonica) for adsorbing heavy metals like mercury from aqueous solutions of different concentrations. The effect of soaking time, pore analyses and chemical properties on the adsorption capabilities of the carbonized materials were discussed. The pH value and chemical oxygen demand (COD) monitored during the soaking period were also described.

  18. Separation of hydrophobic organic compound from surfactant solutions with activated carbon in a fixed bed.

    PubMed

    Liu, Jianfei; Chen, Jiajun; Jiang, Lin; Chen, Cheng

    2013-01-01

    The adsorption behavior of phenanthrene (PHE) in Triton X-100 (TX100) solutions with fixed activated carbon (AC) bed was studied to recover the surfactant. The effect of various parameters like bed depths, flow rates, influent TX100 concentration, and influent PHE concentration were investigated. The breakthrough time of both TX100 and PHE increased with the increase of bed height and decrease of flow rate and influent concentration. In the case of fixed length, a lower flow rate, higher concentration of TX100, and lower concentration of PHE will benefit the longer effective surfactant recovery time. The adsorption data were integrated into bed depth service time models. The height of exchange zone of TX100 should be much shorter than that of PHE, which provides conditions to separate the hydrophobic organic compound from surfactant solutions with AC in a fixed bed. It is likely that the adsorption process is controlled by hydrophobic interaction. PMID:24292481

  19. Variation in assimilable organic carbon formation during chlorination of Microcystis aeruginosa extracellular organic matter solutions.

    PubMed

    Sun, Xingbin; Yuan, Ting; Ni, Huishan; Li, Yanpeng; Hu, Yang

    2016-07-01

    This study investigated the chlorination of Microcystis aeruginosa extracellular organic matter (EOM) solutions under different conditions, to determine how the metabolites produced by these organisms affect water safety and the formation of assimilable organic carbon (AOC). The effects of chlorine dosages, coagulant dosage, reaction time and temperature on the formation of AOC were investigated during the disinfection of M.aeruginosa metabolite solutions. The concentration of AOC followed a decreasing and then increasing pattern with increasing temperature and reaction time. The concentration of AOC decreased and then increased with increasing chlorination dosage, followed by a slight decrease at the highest level of chlorination. However, the concentration of AOC decreased continuously with increasing coagulant dosage. The formation of AOC can be suppressed under appropriate conditions. In this study, chlorination at 4mg/L, combined with a coagulant dose of 40mg/L at 20°C over a reaction time of 12hr, produced the minimum AOC. PMID:27372113

  20. Removal of trihalomethanes from aqueous solution through armchair carbon nanotubes: a molecular dynamics study.

    PubMed

    Azamat, Jafar; Khataee, Alireza; Joo, Sang Woo; Yin, Binfeng

    2015-04-01

    Molecular dynamics simulations were performed to investigate the removal of trihalomethanes (THMs) including CH3Cl, CH2Cl2 and CHCl3 from aqueous solutions by armchair carbon nanotubes (CNTs) under induced pressure. The studied system involved the armchair CNTs embedded between two graphene sheets with an aqueous solution of THMs in the simulation box. An external pressure was applied to the system along the z-axis of the simulation box. Six types of armchair CNTs with different diameter were used in this work, included (4,4), (5,5), (6,6), (7,7), (8,8) and (9,9) CNTs. The results of molecular dynamics simulation display that the armchair CNTs behave differently relative to THMs and water molecules. The permeation of THMs and water molecules through the armchair CNTs was dependent on the diameter of CNTs and the applied pressure. PMID:25682360

  1. Nature of Non-Fickian Solute Transport in Complex Heterogeneous Porous Media - Carbonates

    NASA Astrophysics Data System (ADS)

    Bijeljic, B.; Mostaghimi, P.; Blunt, M. J.

    2011-12-01

    Despite the range of significant practical applications of solute transport, including the long-term fate of nuclear waste repositories, secure storage of CO2 and improved oil recovery, even the qualitative behavior of most rocks is uncertain: vast carbonate sedimentary basins contain more than half the world's current oil reserves yet experimental data on transport in carbonates is scant. The relationship between pore structure, velocity field and transport remains unknown, particularly for heterogeneous carbonates. We simulate solute transport through 3D μ-CT images of different rock samples, representing geological media of increasing pore-scale complexity: a sandpack, a Berea sandstone and a Portland limestone. A finite-difference Stokes solver is employed to compute the flow field and transport particles semi-analytically along streamlines to represent advection with a random motion to model diffusion. We predict the propagators measured on similar cores in Nuclear Magnetic Resonance (NMR) experiments. Dispersion coefficient dependence on Peclet number is shown to have different scaling for complex carbonates. The behavior is explained using continuous time random walks with a truncated power-law distribution of travel times: transport is qualitatively different for the complex limestone compared to the sandstone or sandpack, with long tailing, an almost immobile peak concentration and a very slow approach to asymptotic dispersion. We demonstrate the different nature of non-Fickian transport in carbonates by analyzing the transit time probabilities ψ(τ) of traveling between two neighboring voxels for Portland carbonate that show an approximately power-law dependence of travel times ψ(τ) ~ τ -1-β with a slope corresponding to β = 0.7, as shown in Fig.1. The comparison with ψ(τ) of the sandpack and Berea sandstone for Pe = ∝ indicates quantitatively different generic behavior, as the sandpack and sandstone have slope corresponding to β = 1.8 (two

  2. Pulse Q-Band EPR and ENDOR Spectroscopies of the Photochemically Generated Monoprotonated Benzosemiquinone Radical in Frozen Alcoholic Solution

    PubMed Central

    Flores, Marco; Okamura, Melvin Y.; Niklas, Jens; Pandelia, Maria-Eirini; Lubitz, Wolfgang

    2012-01-01

    Quinones are essential cofactors in many physiological processes, among them proton-coupled electron transfer (PCET) in photosynthesis and respiration. A key intermediate in PCET is the monoprotonated semiquinone radical. In this work we produced the monoprotonated benzosemiquinone (BQH•) by UV illumination of BQ dissolved in 2-propanol at cryogenic temperatures and investigated the electronic and geometric structures of BQH• in the solid state (80 K) using EPR and ENDOR techniques at 34 GHz. The g–tensor of BQH• was found to be similar to that of the anionic semiquinone species (BQ•−) in frozen solution. The peaks present in the ENDOR spectrum of BQH• were identified and assigned by 1H/2H substitutions. The experiments reconfirmed that the hydroxyl proton (O−H) on BQH•, which is abstracted from a solvent molecule, mainly originates from the central CH group of 2-propanol. They also showed that the protonation has a strong impact on the electron spin distribution over the quinone. This is reflected in the hyperfine couplings (hfc’s) of the ring protons, which dramatically changed with respect to those typically observed for BQ•−. The hfc tensor of the O−H proton was determined by a detailed orientation-selection ENDOR study and found to be rhombic, resembling those of protons covalently bound to carbon atoms in a π-system (i.e. α-protons). It was found that the O−H bond lies in the quinone plane and is oriented along the direction of the quinone oxygen lone pair orbital. DFT calculations were performed on different structures of BQH• coordinated by four, three, or zero 2-propanol molecules. The O−H bond length was found to be around 1.0 Å, typical for a single covalent O−H bond. Good agreement between experimental and DFT results were found. This study provides a detailed picture of the electronic and geometric structures of BQH• and should be applicable to other naturally occurring quinones. PMID:22731760

  3. Analytical solutions to dissolved contaminant plume evolution with source depletion during carbon dioxide storage

    NASA Astrophysics Data System (ADS)

    Yang, Yong; Liu, Yongzhong; Yu, Bo; Ding, Tian

    2016-06-01

    Volatile contaminants may migrate with carbon dioxide (CO2) injection or leakage in subsurface formations, which leads to the risk of the CO2 storage and the ecological environment. This study aims to develop an analytical model that could predict the contaminant migration process induced by CO2 storage. The analytical model with two moving boundaries is obtained through the simplification of the fully coupled model for the CO2-aqueous phase -stagnant phase displacement system. The analytical solutions are confirmed and assessed through the comparison with the numerical simulations of the fully coupled model. Then, some key variables in the analytical solutions, including the critical time, the locations of the dual moving boundaries and the advance velocity, are discussed to present the characteristics of contaminant migration in the multi-phase displacement system. The results show that these key variables are determined by four dimensionless numbers, Pe, RD, Sh and RF, which represent the effects of the convection, the dispersion, the interphase mass transfer and the retention factor of contaminant, respectively. The proposed analytical solutions could be used for tracking the migration of the injected CO2 and the contaminants in subsurface formations, and also provide an analytical tool for other solute transport in multi-phase displacement system.

  4. Analytical solutions to dissolved contaminant plume evolution with source depletion during carbon dioxide storage.

    PubMed

    Yang, Yong; Liu, Yongzhong; Yu, Bo; Ding, Tian

    2016-06-01

    Volatile contaminants may migrate with carbon dioxide (CO2) injection or leakage in subsurface formations, which leads to the risk of the CO2 storage and the ecological environment. This study aims to develop an analytical model that could predict the contaminant migration process induced by CO2 storage. The analytical model with two moving boundaries is obtained through the simplification of the fully coupled model for the CO2-aqueous phase -stagnant phase displacement system. The analytical solutions are confirmed and assessed through the comparison with the numerical simulations of the fully coupled model. Then, some key variables in the analytical solutions, including the critical time, the locations of the dual moving boundaries and the advance velocity, are discussed to present the characteristics of contaminant migration in the multi-phase displacement system. The results show that these key variables are determined by four dimensionless numbers, Pe, RD, Sh and RF, which represent the effects of the convection, the dispersion, the interphase mass transfer and the retention factor of contaminant, respectively. The proposed analytical solutions could be used for tracking the migration of the injected CO2 and the contaminants in subsurface formations, and also provide an analytical tool for other solute transport in multi-phase displacement system. PMID:27045163

  5. Na⁺-functionalized carbon quantum dots: a new draw solute in forward osmosis for seawater desalination.

    PubMed

    Guo, Chun Xian; Zhao, Dieling; Zhao, Qipeng; Wang, Peng; Lu, Xianmao

    2014-07-14

    A new type of biocompatible draw solute, Na(+)-functionalized carbon quantum dots (Na_CQDs) with ultra-small size and rich ionic species, in forward osmosis (FO) is developed for seawater desalination. The aqueous dispersion of Na_CQDs demonstrates a high osmotic pressure, which allows high FO water flux and negligible reverse solute permeation. PMID:24870226

  6. Laboratory differential simulation design method of pressure absorbers for carbonization of phenolate solution by carbon dioxide in coal-tar processing

    SciTech Connect

    Linek, V.; Sinkule, J.; Moucha, T.; Rejl, J.F.

    2009-01-15

    A laboratory differential simulation method is used for the design of carbonization columns at coal-tar processing in which phenols are regenerated from phenolate solution by carbon dioxide absorption. The design method is based on integration of local absorption rates of carbon dioxide along the column. The local absorption rates into industrial phenolate mixture are measured in a laboratory model contactor for various compositions of the gas and liquid phases under the conditions that ensure the absorption rates in the laboratory absorber simulate the local rates in the industrial column. On the bases of the calculations, two-step carbonization columns were designed for 30000 t/year of the phenolate solution treatment by carbon dioxide. The absorption proceeds at higher pressure of 500 kPa and temperatures from 50 to 65 C, pure carbon dioxide is used and toluene is added. These conditions have the following favourable effects: (I) significant size reduction of the columns, (ii) it is possible to process more concentrated solutions without danger of silting the columns by crystallization of NaHCO{sub 3} on the packing. (iii) small amount of inert gas is released, (iv) lower alkalinity and better separability of the organic phase (phenols with toluene) from water phase (soda or bicarbonate solution) in separators.

  7. Degradation of triclosan in aqueous solution by dielectric barrier discharge plasma combined with activated carbon fibers.

    PubMed

    Xin, Lu; Sun, Yabing; Feng, Jingwei; Wang, Jian; He, Dong

    2016-02-01

    The degradation of triclosan (TCS) in aqueous solution by dielectric barrier discharge (DBD) plasma with activated carbon fibers (ACFs) was investigated. In this study, ACFs and DBD plasma coexisted in a planar DBD plasma reactor, which could synchronously achieve degradation of TCS, modification and in situ regeneration of ACFs, enhancing the effect of recycling of ACFs. The properties of ACFs before and after modification by DBD plasma were characterized by BET and XPS. Various processing parameters affecting the synergetic degradation of TCS were also investigated. The results exhibited excellent synergetic effects in DBD plasma-ACFs system on TCS degradation. The degradation efficiency of 120 mL TCS with initial concentration of 10 mg L(-1) could reach 93% with 1 mm thick ACFs in 18 min at input power of 80 W, compared with 85% by single DBD plasma. Meanwhile, the removal rate of total organic carbon increased from 12% at pH 6.26-24% at pH 3.50. ACFs could ameliorate the degradation efficiency for planar DBD plasma when treating TCS solution at high flow rates or at low initial concentrations. A possible degradation pathway of TCS was investigated according to the detected intermediates, which were identified by liquid chromatography-hybrid quadrupole time-of-flight mass spectrometry (LC-QTOF-MS) combined with theoretical calculation of Gaussian 09 program. PMID:26421625

  8. Characterization of platinum catalyst supported on carbon nanoballs prepared by solution plasma processing

    SciTech Connect

    Ichin, Yoshimichi; Mitamura, Koji; Saito, Nagahiro; Takai, Osamu

    2009-07-15

    In order to improve the energy-conversion efficiency in fuel cells, the authors loaded Pt nanoparticles on carbon nanoballs (CNBs) by using solution plasma processing (SPP) involving CNB and Pt ion with a protection group. In this study, we employed poly(vinylpyrrolidone) (PVP) or sodium dodecyl sulfate (SDS) to prepare Pt nanoparticles supported on CNB (Pt/CNB) by the SPP, and the electrochemical properties as a catalyst was evaluated by cyclic voltammetry. The carbon nanoballs were prepared by thermal decomposition process of ethylene and hydrogen gases. Color of the solution changed from yellow to dark brown as synthesis time. This change indicates the improvement of dispersibility of CNB. Moreover, transmission electron microscopy images and elemental mapping images showed the Pt nanoparticles supported on CNB. A catalytic activity of the Pt/CNB in use of SDS was shown to be higher than the Pt/CNB prepared with PVP system. The SDS-containing Pt/CNB also showed the higher activity than that obtained by the conventional method.

  9. Effects of carbon source on expression of alcohol oxidase activity and on morphologic pattern of YR-1 Strain, a filamentous fungus isolated from petroleum-contaminated soils.

    PubMed

    Robelo, Carmen Rodríguez; Novoa, Vanesa Zazueta; Zazueta-Sandoval, Roberto

    2004-01-01

    Soluble alcohol oxidase (AO) activity was detected in the supernatant fraction of a high-speed centrifugation procedure after ballistic cellular homo-genization to break the mycelium from a filamentous fungus strain named YR-1, isolated from petroleum-contaminated soils. AO activity from aerobically grown mycelium was detected in growth media containing different carbon sources, including alcohols and hydrocarbons but not in glucose. In previous work, zymogram analysis conducted with crude extracts from aerobic mycelium of YR-1 strain indicated the existence of two AO enzymes originally named AO-1 and AO-2. In the present study, we were able to separate the AO-1 band into two bands depending on culture conditions, carbon source, and polyacrylamide gel electrophoresis (PAGE) separation conditions; the enzyme activity pattern in zymograms from cell-free extracts exhibited three different bands after native PAGE. New nomenclature was used for upper bands AO-1 and AO-2 and lower band AO-3, respectively. The expression of AO activity was studied in the absence of glucose in the culture media and in the presence of hydrocarbons or petroleum as sole carbon source, suggesting that AO expression could be subjected to two regulatory possibilities: carbon catabolite regulation by glucose and induction by hydrocarbons. The possibility of catabolic inhibition of AO by glucose in the active enzyme was also tested, and the results confirm that this kind of regulatory mechanism is not present in AO activity. PMID:15054203

  10. Cryogenic-temperature electron microscopy direct imaging of carbon nanotubes and graphene solutions in superacids.

    PubMed

    Kleinerman, O; Parra-Vasquez, A Nicholas G; Green, M J; Behabtu, N; Schmidt, J; Kesselman, E; Young, C C; Cohen, Y; Pasquali, M; Talmon, Y

    2015-07-01

    Cryogenic electron microscopy (cryo-EM) is a powerful tool for imaging liquid and semiliquid systems. While cryogenic transmission electron microscopy (cryo-TEM) is a standard technique in many fields, cryogenic scanning electron microscopy (cryo-SEM) is still not that widely used and is far less developed. The vast majority of systems under investigation by cryo-EM involve either water or organic components. In this paper, we introduce the use of novel cryo-TEM and cryo-SEM specimen preparation and imaging methodologies, suitable for highly acidic and very reactive systems. Both preserve the native nanostructure in the system, while not harming the expensive equipment or the user. We present examples of direct imaging of single-walled, multiwalled carbon nanotubes and graphene, dissolved in chlorosulfonic acid and oleum. Moreover, we demonstrate the ability of these new cryo-TEM and cryo-SEM methodologies to follow phase transitions in carbon nanotube (CNT)/superacid systems, starting from dilute solutions up to the concentrated nematic liquid-crystalline CNT phases, used as the 'dope' for all-carbon-fibre spinning. Originally developed for direct imaging of CNTs and graphene dissolution and self-assembly in superacids, these methodologies can be implemented for a variety of highly acidic systems, paving a way for a new field of nonaqueous cryogenic electron microscopy. PMID:25818279

  11. Rethinking Coal: Thin Films of Solution Processed Natural Carbon Nanoparticles for Electronic Devices.

    PubMed

    Keller, Brent D; Ferralis, Nicola; Grossman, Jeffrey C

    2016-05-11

    Disordered carbon materials, both amorphous and with long-range order, have been used in a variety of applications, from conductive additives and contact materials to transistors and photovoltaics. Here we show a flexible solution-based method of preparing thin films with tunable electrical properties from suspensions of ball-milled coals following centrifugation. The as-prepared films retain the rich carbon chemistry of the starting coals with conductivities ranging over orders of magnitude, and thermal treatment of the resulting films further tunes the electrical conductivity in excess of 7 orders of magnitude. Optical absorption measurements demonstrate tunable optical gaps from 0 to 1.8 eV. Through low-temperature conductivity measurements and Raman spectroscopy, we demonstrate that variable range hopping controls the electrical properties in as-prepared and thermally treated films and that annealing increases the sp(2) content, localization length, and disorder. The measured hopping energies demonstrate electronic properties similar to amorphous carbon materials and reduced graphene oxide. Finally, Joule heating devices were fabricated from coal-based films, and temperatures as high as 285 °C with excellent stability were achieved. PMID:27031328

  12. Carbon nanotubes dispersed in aqueous solution by ruthenium(ii) polypyridyl complexes.

    PubMed

    Huang, Kewei; Saha, Avishek; Dirian, Konstantin; Jiang, Chengmin; Chu, Pin-Lei E; Tour, James M; Guldi, Dirk M; Martí, Angel A

    2016-07-21

    Cationic ruthenium(ii) polypyridyl complexes with appended pyrene groups have been synthesized and used to disperse single-walled carbon nanotubes (SWCNT) in aqueous solutions. To this end, planar pyrene groups enable association by means of π-stacking onto carbon nanotubes and, in turn, the attachment of the cationic ruthenium complexes. Importantly, the ionic nature of the ruthenium complexes allows the formation of stable dispersions featuring individualized SWCNTs in water as confirmed in a number of spectroscopic and microscopic assays. In addition, steady-state photoluminescence spectroscopy was used to probe the excited state interactions between the ruthenium complexes and SWCNTs. These studies show that the photoluminescence of both, that is, of the ruthenium complexes and of SWCNTs, are quenched when they interact with each other. Pump-probe transient absorption experiments were performed to shed light onto the nature of the photoluminescence quenching, showing carbon nanotube-based bands with picosecond lifetimes, but no new bands which could be unambigously assigned to photoinduced charge transfer process. Thus, from the spectroscopic data, we conclude that quenching of the photoluminescence of the ruthenium complexes is due to energy transfer to proximal SWCNTs. PMID:27353007

  13. Carbonation of municipal solid waste incineration electrostatic precipitator fly ashes in solution.

    PubMed

    De Boom, Aurore; Aubert, Jean-Emmanuel; Degrez, Marc

    2014-05-01

    Carbonation was applied to a Pb- and Zn-contaminated fraction of municipal solid waste incineration electrofilter fly ashes in order to reduce heavy metal leaching. Carbonation tests were performed in solution, by Na2CO3 addition or CO2 bubbling, and were compared with washing (with water only). The injection of CO2 during the washing did not modify the mineralogy, but the addition of Na2CO3 induced the reaction with anhydrite, forming calcite. Microprobe analyses showed that Pb and Zn contamination was rather diffuse and that the various treatments had no effect on Pb and Zn speciation in the residues. The leaching tests indicated that carbonation using Na2CO3 was successful because it gave a residue that could be considered as non-hazardous material. With CO2 bubbling, Pb and Zn leaching was strongly decreased compared with material washed with water alone, but the amount of chromium extracted became higher than the non-hazardous waste limits for landfilling. PMID:24718362

  14. Ultrasound-assisted adsorption of 4-dodecylbenzene sulfonate from aqueous solutions by corn cob activated carbon.

    PubMed

    Milenković, D D; Bojić, A Lj; Veljković, V B

    2013-05-01

    This study was aimed at removal of 4-dodecylbenzene sulfonate (DBS) ions from aqueous solutions by ultrasound-assisted adsorption onto the carbonized corn cob (AC). The main attention was focused on modeling the equilibrium and kinetics of adsorption of DBS onto the AC. The AC was prepared from ground dried corn cob by carbonization and activation by carbon dioxide at 880°C for 2h in a rotary furnace. The adsorption isotherm data were fitted by the Langmuir model in both the absence and the presence of ultrasound (US). The maximum adsorption capacities of the adsorbent for DBS, calculated from the Langmuir isotherms, were 29.41mg/g and 27.78mg/g in the presence of US and its absence, respectively. The adsorption process in the absence and the presence of US obeyed the pseudo second-order kinetics. The intraparticular diffusion model indicated that the adsorption of DBS ions on the AC was diffusion controlled as well as that US promoted intraparticular diffusion. The ΔG° values, -24.03kJ/mol, -25.78kJ/mol and -27.78kJ/mol, were negative at all operating temperatures, verifying that the adsorption of DBS ions was spontaneous and thermodynamically favorable. The positive value of ΔS°=187J/molK indicated the increased randomness at the adsorbent-adsorbate interface during the adsorption of DBS ions by the AC. PMID:23187067

  15. Corrosion behavior of titanium alloy Beta-21S coated with diamond like carbon in Hank's solution

    NASA Astrophysics Data System (ADS)

    Mohan, L.; Anandan, C.; Grips, V. K. William

    2012-06-01

    Diamond like carbon (DLC) coatings posses high hardness and low friction coefficient and also biocompatible, hence, they are of interest for enhancing the wear and corrosion resistance of bio-implant materials. Beta stabilized titanium alloys are attractive for biomedical applications because of their high specific strength and low modulus. In this work Beta-21S alloy (Ti-15Mo-3Nb-3Al-0.2Si) was implanted with carbon ions by plasma immersion ion implantation using methane and hydrogen gas mixture followed by DLC deposition by plasma enhanced chemical vapour deposition (PECVD). The implanted layers enabled deposition of adherent diamond-like carbon coatings on the titanium alloy which was otherwise not possible. The corrosion behavior of the treated and untreated samples was investigated through electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization studies in simulated body fluid (Hank's solution). XPS, micro Raman and EDAX investigation of the samples showed the formation of a thin oxide layer on the treated samples after corrosion experiments. Corrosion resistance of the DLC coated sample is comparable with that of the untreated samples. Electrochemical impedance data of the substrate and implanted samples were fitted with two time constant equivalent circuits and that of DLC coated samples with two-layer model.

  16. Alcohol Alert

    MedlinePlus

    ... Us You are here Home » Alcohol Alert Alcohol Alert The NIAAA Alcohol Alert is a quarterly bulletin that disseminates important research ... text. To order single copies of select Alcohol Alerts, see ordering Information . To view publications in PDF ...

  17. Alcoholism - resources

    MedlinePlus

    Resources - alcoholism ... The following organizations are good resources for information on alcoholism : Alcoholics Anonymous -- www.aa.org Al-Anon/Alateen -- www.al-anon.org/home National Institute on Alcohol ...

  18. Alcoholic ketoacidosis

    MedlinePlus

    Ketoacidosis - alcoholic ... Alcoholic ketoacidosis is caused by very heavy alcohol use. It most often occurs in a malnourished person ... Symptoms of alcoholic ketoacidosis include: Nausea and vomiting ... Changed level of alertness, which may lead to coma Confusion ...

  19. Alcohol Facts

    MedlinePlus

    ... raquo Alcohol Facts Alcohol Facts Listen Drinks like beer, malt liquor, wine, and hard liquor contain alcohol. Alcohol is the ingredient that gets you drunk. Hard liquor—such as whiskey, rum, or gin—has more ...

  20. Alcoholic neuropathy

    MedlinePlus

    Neuropathy - alcoholic; Alcoholic polyneuropathy ... The exact cause of alcoholic neuropathy is unknown. It likely includes both a direct poisoning of the nerve by the alcohol and the effect of poor nutrition ...

  1. Hydrogenophaga carboriunda sp. nov., a tertiary butyl alcohol-oxidizing, psychrotolerant aerobe derived from granular-activated carbon (GAC).

    PubMed

    Reinauer, Kimberly M; Popovic, Jovan; Weber, Christopher D; Millerick, Kayleigh A; Kwon, Man Jae; Wei, Na; Zhang, Yang; Finneran, Kevin T

    2014-04-01

    A Gram-negative, rod-shaped bacterium was isolated from a mixed culture that degraded tert-butyl alcohol (TBA) in a granular-activated carbon (GAC) sample from a Biological-GAC reactor. Strain YZ2(T) was assigned to the Betaproteobacteria within the family Comamonadaceae based on 16S rRNA gene similarities. The nearest phylogenetic relative (95.0 % similarity) with a valid name was Hydrogenophaga taeniospiralis. The DNA G+C content was 66.4 mol%. DNA:DNA hybridization indicated that the level of relatedness to members of the genus Hydrogenophaga ranged from 1.1 to 10.8 %. The dominant cellular fatty acids were: 18:1 w7c (75 %), 16:0 (4.9 %), 17:0 (3.85 %), 18:0 (2.93 %), 11 methyl 18:1 w7c (2.69 %), Summed Feature 2 (2.27 %), and 18:0 3OH (1.35 %). The primary substrate used was TBA, which is a fuel oxygenate and groundwater contaminant. YZ2(T) was non-motile, without apparent flagella. It is a psychrotolerant, facultative aerobe that grew between pH 6.5 and 9.5, and 4 and 30 °C. The culture grew on and mineralized TBA at 4 °C, which is the first report of psychrotolerant TBA degradation. Hydrogen was used as an alternative electron donor. The culture also grew well in defined freshwater medium with ethanol, butanol, hydroxy isobutyric acid, acetate, pyruvate, citrate, lactate, isopropanol, and benzoic acid as electron donors. Nitrate was reduced with hydrogen as the sole electron donor. On the basis of morphological, physiological, and chemotaxonomic data, a new species, Hydrogenophaga carboriunda is proposed, with YZ2(T) as the type strain. PMID:24343174

  2. Radiation-crosslinking of shape memory polymers based on poly(vinyl alcohol) in the presence of carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Basfar, A. A.; Lotfy, S.

    2015-01-01

    Shape memory polymers based on poly(vinyl alcohol) (SM-PVA) in the presence of 2-carboxyethyl acrylate oligomers (CEA) and multi-wall carbon nanotubes (MWCNTs) crosslinked by ionizing radiation were investigated. Chemical-crosslinking of PVA by glutaraldehyde in the presence of CEA and MWCNTs was also studied. The swelling and gel fraction of the radiation-crosslinked SM-PVA and chemically crosslinked systems were evaluated. Analysis of the swelling and gel fraction revealed a significant reduction in swelling and an increase in the gel fraction of the material that was chemically crosslinked with glutaraldehyde. The radiation-crosslinked SM-PVA demonstrated 100% gelation at an irradiation dose of 50 kGy. In addition, radiation-crosslinked SM-PVA exhibited good temperature responsive shape-memory behavior. A scanning electron microscopy (SEM) analysis was performed. The thermal properties of radiation-crosslinked SM-PVA were investigated by a thermogravimetric analysis (TGA) and dynamic mechanical analysis (DMA). The ability of the material to return or store energy (E‧), to its ability to lose energy (E″), and the ratio of these effects (Tanδ), which is called damping were examined via DMA. The temperature of Tanδ in the radiation-crosslinked SM-PVA decreased significantly by 6 and 13 °C as a result of the addition of MWCNTs. In addition, the temperature of Tanδ for SM-PVA increased as the irradiation dose increased. These radiation-crosslinked SM-PVA materials show promising shape-memory behavior based on the range of temperatures at which Tanδ appears.

  3. [Studies on carbonization of saccharides by using aqueous solution of various acids].

    PubMed

    Zhang, Xin; He, An-Qi; Kang, Ting-Guo; Xia, Jin-Ming; Weng, Shi-Fu; Xu, Yi-Zhuang; Wu, Jin-Guang

    2014-09-01

    The authors tried to establish an approach to use acids to convert biomass into a fuel with higher carbon content and lower oxygen content in a zero-energy-consumption fashion. Considering that biomass is composed of monosaccharide, we used aqueous solutions of variation acids including hydrochloric acid, sulfuric acid and perchloric acid to treat 2-deoxy-ribose and fructose at ambient temperature and pressure. Black substances were produced after a period of time when 2-deoxy-ribose and fructose were mixed with aqueous solutions containing 8 mol · L(-1) acids. The black substance was collected and characterized by using elemental analysis, Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). Elemental analysis results indicate that the contents of carbon increases significantly in the black substances in comparison with 2-deoxy-ribose and fructose. Moreover, XPS results indicate that the content of oxygen in the black substance undergoes a significant decrease compared with pure 2-deoxy-ribose and fructose. In the XPS spectra, the is peaks of 2-deoxy-ribose, strong sub peak at 286. 05 eV, which is assigned to carbon linked to oxygen directly, dominate in the C is peak envelop. After treatment by HClO4, the peak decreased dramatically. This result also supports the conclusion that the content of oxygen in mono-saccharide is significantly reduced after treatment by acids. In the FTIR spectra of the black substances, strong peaks can be observed around 1 600 cm(-1), indicating that C==C bond is formed in the product. The above results suggest that treatments with acids may be developed as a new zero-energy-consumption approach to convert biomass in a new fuel with improved energy output efficiency. PMID:25532323

  4. Solute Export and Carbon Dioxide Trends of the Altamaha River Basin

    NASA Astrophysics Data System (ADS)

    Vuong, C. K.; Patel, K.; Karim, A.

    2007-12-01

    The Altamaha River Basin (ARB), a major drainage of the Atlantic seaboard, was monitored near Jesup, Georgia, on a biweekly frequency during April 2006 through June 2007. Alkalinity, pH, temperature, and Total Dissolved Solids (TDS) were measured in the field. Geographic Information Systems and historical precipitation and stream flow were used to calculate mean annual: (1) precipitation flux into the basin; (2) runoff from the basin; (3) solute export; and (4) partial pressure of carbon dioxide (pCO2). The mean annual precipitation flux to the ARB is 46.4 km3. Runoff near the mouth of the Altamaha River is 12.1 km3 or about 26% of the precipitation input, implying that roughly three quarters of all the rain that falls on the basin is lost to evapotranspiration. The ARB has discharge-weighted average TDS concentration of 53.3 mg/L and annually exports 646,445 metric tons of dissolved solutes to the Atlantic Ocean. The pCO2 values range between close to atmospheric equilibrium in May to 106 times above atmospheric equilibrium in December. For the rising limb of the hydrograph, pCO2 trend mimics stream flow with pCO2 peak occurring about a month ahead of discharge. The low values probably indicate CO2 drawdown by aquatic photosynthesis and higher values indicate discharge of wastewater/shallow groundwater charged with bacterially respired carbon dioxide. Thus, the ARB was a net source of carbon dioxide to the atmosphere during the water year 2006-2007.

  5. Solution-Processed Carbon Nanotube and Chemically Synthesized Graphene Nanoribbon Field Effect Transistors

    NASA Astrophysics Data System (ADS)

    Bennett, Patrick Bryce

    Carbon nanotubes (CNTs) possess great potential as high performance semiconducting channels due to their one-dimensional nature, extremely high mobility, and their demonstrated ability to transport electrons ballistically in transistors. However, the presence of metallic CNTs in CNT films and arrays represents a major impediment towards large-scale integration. Methods of solution purification have demonstrated partial success in metallic CNT removal, although their effects on device performance are unknown. While this problem may be solvable, new synthesis techniques have recently resulted in the creation of high-density films of graphene nanoribbons (GNRs) with atomically smooth edges, uniform widths, and uniform band structure. These may ultimately supplant CNTs in device applications due to their theoretically similar, but uniform electronic properties. This work aims to study the effects of purification of semiconducting CNTs in thin film transistors (TFTs) and to develop methods to increase device performance when metallic CNTs are present. Devices consisting of large networks of CNTs as well as short channel, single CNT devices are characterized to determine the effects of solution processing on CNTs themselves. Short channel, bottom-up GNR devices are fabricated to compare their performance to CNT transistors. The first half of this dissertation describes the methods of integrating CNTs from various sources into transistors. Growth and transfer are described, as well as methods of creating aqueous suspensions for solution processing. Development of novel surfactant materials based on biomimetic polymers used to suspend CNTs in solution are reported and characterized. Methods of deposition out of solution and onto insulating substrates are covered. Device fabrication from start to finish is detailed, with the subtleties of processing required to produce sub 10-nm channel length devices explained. The second half reports devices produced via these techniques

  6. Adsorption of Direct Blue 53 dye from aqueous solutions by multi-walled carbon nanotubes and activated carbon.

    PubMed

    Prola, Lizie D T; Machado, Fernando M; Bergmann, Carlos P; de Souza, Felipe E; Gally, Caline R; Lima, Eder C; Adebayo, Matthew A; Dias, Silvio L P; Calvete, Tatiana

    2013-11-30

    Multi-walled carbon nanotubes (MWCNT) and powder activated carbon (PAC) were used as adsorbents for adsorption of Direct Blue 53 dye (DB-53) from aqueous solutions. The adsorbents were characterised using Raman spectroscopy, N2 adsorption/desorption isotherms, and scanning and transmission electron microscopy. The effects of initial pH, contact time and temperature on adsorption capacity of the adsorbents were investigated. At pH 2.0, optimum adsorption of the dye was achieved by both adsorbents. Equilibrium contact times of 3 and 4 h were achieved by MWCNT and PAC adsorbents, respectively. The general order kinetic model provided the best fit of the experimental data compared to pseudo-first order and pseudo-second order kinetic adsorption models. For DB-53 dye, the equilibrium data (298-323 K) were best fitted to the Sips isotherm model. The maximum sorption capacity for adsorption of the dye occurred at 323 K, with the values of 409.4 and 135.2 mg g(-1) for MWCNT and PAC, respectively. Studies of adsorption/desorption were conducted and the results showed that DB-53 loaded MWCNT could be regenerated (97.85%) using a mixture 50% acetone + 50% of 3 mol L(-1) NaOH. Simulated dye house effluents were used to evaluate the application of the adsorbents for effluent treatment (removal of 99.87% and 97.00% for MWCNT and PAC, respectively, were recorded). PMID:24076517

  7. Covalent cum noncovalent functionalizations of carbon nanotubes for effective reinforcement of a solution cast composite film.

    PubMed

    Yuan, Wei; Chan-Park, Mary B

    2012-04-01

    Although carbon nanotubes have impressive tensile properties, exploiting these properties in composites, especially those made by the common solution casting technique, seems to be elusive thus far. The reasons could be partly due to the poor nanotube dispersion and the weak nanotube/matrix interface. To solve this dual pronged problem, we combine noncovalent and covalent functionalizations of nanotubes in a single system by the design and application of a novel dispersant, hydroxyl polyimide-graft-bisphenol A diglyceryl acrylate (PI(OH)-BDA), and use them with epoxidized single-walled carbon nanotubes (O-SWNTs). Our novel PI(OH)-BDA dispersant functionalizes the nanotubes noncovalently to achieve good dispersion of the nanotubes because of the strong π-π interaction due to main chain and steric hindrance of the BDA side chain. PI(OH)-BDA also functionalizes O-SWNTs covalently because it reacts with epoxide groups on the nanotubes, as well as the cyanate ester (CE) matrix used. The resulting solution-cast CE composites show 57%, 71%, and 124% increases in Young's modulus, tensile strength, and toughness over neat CE. These values are higher than those of composites reinforced with pristine SWNTs, epoxidized SWNTs, and pristine SWNTs dispersed with PI(OH)-BDA. The modulus and strength increase per unit nanotube weight fraction, i.e., dE/dW(NT) and dσ/dW(NT), are 175 GPa and 7220 MPa, respectively, which are significantly higher than those of other nanotube/thermosetting composites (22-70 GPa and 140-3540 MPa, respectively). Our study indicates that covalent cum noncovalent functionalization of nanotubes is an effective tool for improving both the nanotube dispersion and nanotube/matrix interfacial interaction, resulting in significantly improved mechanical reinforcement of the solution-cast composites. PMID:22432973

  8. Linking mineralisation process and sedimentary product in terrestrial carbonates using a solution thermodynamic approach

    NASA Astrophysics Data System (ADS)

    Rogerson, M.; Pedley, H. M.; Kelham, A.; Wadhawan, J. D.

    2014-04-01

    Determining the processes which generate terrestrial carbonate deposits (tufas, travertines and to a lesser extent associated chemical sediments such as calcretes and speleothems) is a long-standing problem. Precipitation of mineral products from solution reflects a complex combination of biological, equilibrium and kinetic processes, and the different morphologies of carbonate sediment produced by different processes have yet to be clearly demarked. Building on the groundbreaking work of previous authors, we propose that the underlying control on the processes leading to the deposition of these products can be most parsimoniously understood from the thermodynamic properties of their source solutions. Here, we report initial observations of the differences in product generated from spring and lake systems spanning a range of temperature-supersaturation space. We find that at high supersaturation, biological influences are masked by high rates of physico-chemical precipitation, and sedimentary products from these settings infrequently exhibit classic "biomediated" fabrics such as clotted micrite. Likewise, at high temperature (>40 °C) exclusion of vascular plants and complex/diverse biofilms can significantly inhibit the magnitude of biomediated precipitation, again impeding the likelihood of encountering the "bio-type" fabrics. Conversely, despite the clear division in product between extensive tufa facies associations and less spatially extensive deposits such as oncoid beds, no clear division can be identified between these systems in temperature-supersaturation space. We reiterate the conclusion of previous authors, which demonstrate that this division cannot be made on the basis of physico-chemical characteristics of the solution alone. We further provide a new case study of this division from two adjacent systems in the UK, where tufa-like deposition continuous on a metre scale is happening at a site with lower supersaturation than other sites exhibiting only

  9. Adsorption of tetracycline from aqueous solutions onto multi-walled carbon nanotubes with different oxygen contents

    PubMed Central

    Yu, Fei; Ma, Jie; Han, Sheng

    2014-01-01

    Oxidized multi-walled carbon nanotubes (MWCNTs) with different oxygen contents were investigated for the adsorption of tetracycline (TC) from aqueous solutions. As the surface oxygen content of the MWCNTs increased, the maximum adsorption capacity and adsorption coefficient of TC increased to the largest values and then decreased. The relation can be attributed to the interplay between the nanotubes' dispersibility and the water cluster formation upon TC adsorption. The overall adsorption kinetics of TC onto CNTs-3.2%O might be dependent on both intra-particle diffusion and boundary layer diffusion. The maximum adsorption capacity of TC on CNTs-3.2%O was achieved in the pH range of 3.3–8.0 due to formation of water clusters or H-bonds. Furthermore, the presence of Cu2+ could significantly enhanced TC adsorption at pH of 5.0. However, the solution ionic strength did not exhibit remarkable effect on TC adsorption. In addition, when pH is beyond the range (3.3–8.0), the electrostatic interactions caused the decrease of TC adsorption capacity. Our results indicate that surface properties and aqueous solution chemistry play important roles in TC adsorption on MWCNTs. PMID:24937315

  10. Microwave-induced carbon nanotubes catalytic degradation of organic pollutants in aqueous solution.

    PubMed

    Chen, Jing; Xue, Shuang; Song, Youtao; Shen, Manli; Zhang, Zhaohong; Yuan, Tianxin; Tian, Fangyuan; Dionysiou, Dionysios D

    2016-06-01

    In this study, a new catalytic degradation technology using microwave induced carbon nanotubes (MW/CNTs) was proposed and applied in the treatment of organic pollutants in aqueous solution. The catalytic activity of three CNTs of 10-20nm, 20-40nm, and 40-60nm diameters were compared. The results showed that organic pollutants such as methyl orange (MO), methyl parathion (MP), sodium dodecyl benzene sulfonate (SDBS), bisphenol A (BPA), and methylene blue (MB) in aqueous solution could be degraded effectively and rapidly in MW/CNTs system. CNTs with diameter of 10-20nm exhibited the highest catalytic activity of the three CNTs under MW irradiation. Further, complete degradation was obtained using 10-20nm CNTs within 7.0min irradiation when 25mL MO solution (25mg/L), 1.2g/L catalyst dose, 450W, 2450MHz, and pH=6.0 were applied. The rate constants (k) for the degradation of SDBS, MB, MP, MO and BPA using 10-20nm CNTs/MW system were 0.726, 0.679, 0.463, 0.334 and 0.168min(-1), respectively. Therefore, this technology may have potential application for the treatment of targeted organic pollutants in wastewaters. PMID:26937869

  11. Adsorption of tetracycline from aqueous solutions onto multi-walled carbon nanotubes with different oxygen contents

    NASA Astrophysics Data System (ADS)

    Yu, Fei; Ma, Jie; Han, Sheng

    2014-06-01

    Oxidized multi-walled carbon nanotubes (MWCNTs) with different oxygen contents were investigated for the adsorption of tetracycline (TC) from aqueous solutions. As the surface oxygen content of the MWCNTs increased, the maximum adsorption capacity and adsorption coefficient of TC increased to the largest values and then decreased. The relation can be attributed to the interplay between the nanotubes' dispersibility and the water cluster formation upon TC adsorption. The overall adsorption kinetics of TC onto CNTs-3.2%O might be dependent on both intra-particle diffusion and boundary layer diffusion. The maximum adsorption capacity of TC on CNTs-3.2%O was achieved in the pH range of 3.3-8.0 due to formation of water clusters or H-bonds. Furthermore, the presence of Cu2+ could significantly enhanced TC adsorption at pH of 5.0. However, the solution ionic strength did not exhibit remarkable effect on TC adsorption. In addition, when pH is beyond the range (3.3-8.0), the electrostatic interactions caused the decrease of TC adsorption capacity. Our results indicate that surface properties and aqueous solution chemistry play important roles in TC adsorption on MWCNTs.

  12. Transport of carbon, nitrogen, phosphorus, and major solutes in the Gambia River, West Africa

    SciTech Connect

    Lesack, L.F.W.; Hecky, R.E.; Melack, J.M.

    1984-07-01

    Transport of solutes and particulate materials and their variation with discharge were studied for 1 year (July 1980-June 1981) in the Gambia River in the tropical savanna of West Africa. The water is a dilute solution of SiO/sub 2/ and HCO/sub 3//sup -/. Na/sup +/, K/sup +/, Cl/sup -/, and total dissolved nitrogen showed no significant relation with discharge. Ca/sup 2 +/, Mg/sup 2 +/, HCO/sub 3//sup -/, conductivity, and SO/sub 4//sup 2 -/ decreased as discharge increased, while total dissolved phosphorus increased with discharge. After an initial increase SiO/sub 2/ was independent of discharge. Dissolved organic carbon displayed counterclockwise hysteresis with rising and falling discharge. Particulate phosphorus and total particulate materials displayed clockwise hysteresis. Total transport amounted to 9.66 t x km/sup -2/ x yr/sup -1/. The transport rates of both dissolved and particulate organic C are among the lowest ever reported. The low transport of total particulates and solutes is attributed to lack of relief and the lithology of the catchment.

  13. Alcohol Alert: Genetics of Alcoholism

    MedlinePlus

    ... and Reports » Alcohol Alert » Alcohol Alert Number 84 Alcohol Alert Number 84 Print Version The Genetics of ... immune defense system. Genes Encoding Enzymes Involved in Alcohol Breakdown Some of the first genes linked to ...

  14. Water movement and solute transport in permafrost wetlands: implications for inorganic carbon cycling

    NASA Astrophysics Data System (ADS)

    Jessen, Søren; Dahl Holmslykke, Hanne; Rasmussen, Kristine; Richardt, Niels; Engelund Holm, Peter

    2014-05-01

    Carbon dioxide emissions from thawing permafrost wetlands are an expected consequence of global warming. Addressing the pathways by which carbon is emitted, we investigated the hydrological and geochemical controls on the pore water chemistry of a permafrost wetland, with a shallow geological sequence comprising loam overlain by sphagnum peat, in Ilulissat, Greenland. A 400 m transect parallel to the general flow direction was established, along which water table measurements and slug tests were conducted, and the active layer thickness recorded (typically ~0.5 m). Also, in three detailed profiles along the transect, the vertical distributions of stable isotopes of water and major ion chemistry were investigated, by analysis of active layer pore water and water of melted core sections of permafrost. Concentrations of chloride (0.3-0.4 mM) did not show variation with depth, dismissing solute movement by ion freeze-out during fall freeze-up as a main control on the water chemistry. In addition, the observed vertical δ18O distribution did not to any extent conform to modelled Rayleigh distillation curves for the preferential inclusion of H218O into ice, which could be a scenario for fall freeze-up. The δ18O data therefore suggests either a rapid freeze-up or a simultaneous phase transition at all depths of the active layer, which in either case also would minimize potential ion freeze-out effects. Nevertheless, concentrations of major ions generally increased with depth. A conceptual model for water and solute transport was therefore established, according to which solutes are mobilized by weathering reactions in the loam and then transported upwards to the peat by diffusion. In the peat, lateral advective solute transport dominates. We applied the model to observed profiles of Ca, Mg, HCO3 and the partial CO2 pressure (PCO2). Concentrations of Ca, Mg and HCO3 increased with depth, reaching ~2 mM, ~2 mM and ~8 meq/L at the bottom of the active layer. Pore water at

  15. Electrosorption of ions from aqueous solutions with carbon nanotubes and nanofibers composite film electrodes

    SciTech Connect

    Wang, X. Z.; Li, M. G.; Chen, Y. W.; Cheng, R. M.; Huang, S. M.; Pan, L. K.; Sun, Z.

    2006-07-31

    Electrosorption of ions from aqueous solutions with carbon nanotubes and nanofibers (CNTs-CNFs) composite film electrodes has been demonstrated. The large area CNTs-CNFs film was directly grown on Ni plate by low pressure and low temperature thermal chemical vapor deposition. The CNTs-CNFs electrodes have great advantages such as low cost, easy operation, long-term reproducibility, and integrity of monolithic CNTs-CNFs film and current collector. Batch-mode experiments at low voltage (0.4-2 V) were conducted in a continuously recycling system to investigate the electrosorption process. Purification of water with good reproducibility was achieved because of optimal pore size distribution of CNTs-CNFs composite films.

  16. Electrostatic charge and interactions within carbon-nanotube nematic in electrolyte solution

    NASA Astrophysics Data System (ADS)

    Lee, Choong-Seop; Yakobson, Boris I.

    2004-03-01

    The lyotropic transitions from isotropic solution (I) to nematic liquid crystalline phases (N, N') of single-wall carbon nanotubes (SWNT) are guided by the volumetric fraction together with the electrostatic forces. The latter depends on charge transfer between the SWNT and the solvent-electrolyte, and can be studied in approach similar to Derjaguin-Landau-Verwey-Overbeek. A simple kinetic model for a charging mechanism of SWNT is proposed, which allows analytical treatment. We have explored the optimization of control parameters (equilibrium constants, temperature, pH, etc.) of the model to achieve the separation of densely packed SWNT-bundle (N) into array of spaced individual tubules (N'). Our results explain the observation in recent experiments [1] of the dispersion of SWNT in oleum (overconcentrated sulpheric acid) as well as the sudden collapse of such dispersion with small amount of water added. [1] M. Pasquali et al., Macromolecules (in press).

  17. Removal of dyes from aqueous solutions using activated carbon prepared from rice husk residue.

    PubMed

    Li, Yaxin; Zhang, Xian; Yang, Ruiguang; Li, Guiying; Hu, Changwei

    2016-01-01

    The treatment of dye wastewater by activated carbon (AC) prepared from rice husk residue wastes was studied. Batch adsorption studies were conducted to investigate the effects of contact time, initial concentration (50-450 mg/L), pH (3-11) and temperature (30-70 °C) on the removal of methylene blue (MB), neutral red, and methyl orange. Kinetic investigation revealed that the adsorption of dyes followed pseudo-second-order kinetics. The results suggested that AC was effective to remove dyes, especially MB, from aqueous solutions. Desorption studies found that chemisorption by the adsorbent might be the major mode of dye removal. Fourier transform infrared results suggested that dye molecules were likely to combine with the O-H and P=OOH groups of AC. PMID:26942535

  18. Thermally and Environmentally Stable Carrier Doping Using a Solution Method in Carbon Nanotube Films

    NASA Astrophysics Data System (ADS)

    Sasaki, Yorihiko; Okimoto, Haruya; Yoshida, Kenji; Ono, Yasuichi; Iwasa, Yoshihiro; Takenobu, Taishi

    2011-08-01

    In the present paper, we report the thermal stability of a single-walled carbon nanotube (SWCNT) film that was doped using tetrafluorotetracyano-p-quinodimethane (F4TCNQ). The SWCNTs were doped using a vapor method and a solution method, and their thermostabilities were characterized using a gas chromatography/mass spectrometer (GC/MS) and resistance measurements. These measurements clearly demonstrated the high thermal stability of F4TCNQ and the strong charge-transfer interaction between the SWCNTs and the dopants. As a result, we successfully observed an excellent long-term (longer than 500 h) thermal resistance up to 150 °C, which is a sufficient level of stability for the practical use of this dopant.

  19. Kinetic study of carbon dioxide reaction with tertiary amines in aqueous solutions

    SciTech Connect

    Barth, D.; Tondre, C.; Lappai, G.; Delpuech, J.J.

    1981-11-26

    Reaction kinetics of CO/sub 2/ with triethanolamine (TEA) and methyldiethanolamine (MDEA) in aqueous solution have been studied by using a stopped-flow technique with pH detection. Rate constants are obtained from the comparison of experimental and theoretical curves giving the optical density as a function of time. At concentrations of CO/sub 2/ well below the saturation limit, the results are consistent with the hydration reactions of the CO/sub 2/ molecules either with neutral water molecules or with hydroxide ions, depending upon the pH, itself governed by the ionization equilibrium of the dissolved amine. Moreover, a specific (catalytic) reaction, first order with respect to both carbon dioxide and amine (rate constant, 2.85 M/sup -1/ s/sup -1/ at 25/sup 0/C), has been shown to contribute significantly to the reaction rate in the case of the first amine (TEA) only.

  20. Electrosorption of ions from aqueous solutions with carbon nanotubes and nanofibers composite film electrodes

    NASA Astrophysics Data System (ADS)

    Wang, X. Z.; Li, M. G.; Chen, Y. W.; Cheng, R. M.; Huang, S. M.; Pan, L. K.; Sun, Z.

    2006-07-01

    Electrosorption of ions from aqueous solutions with carbon nanotubes and nanofibers (CNTs-CNFs) composite film electrodes has been demonstrated. The large area CNTs-CNFs film was directly grown on Ni plate by low pressure and low temperature thermal chemical vapor deposition. The CNTs-CNFs electrodes have great advantages such as low cost, easy operation, long-term reproducibility, and integrity of monolithic CNTs-CNFs film and current collector. Batch-mode experiments at low voltage (0.4-2V) were conducted in a continuously recycling system to investigate the electrosorption process. Purification of water with good reproducibility was achieved because of optimal pore size distribution of CNTs-CNFs composite films.

  1. Carbon nanotubes dispersed in aqueous solution by ruthenium(ii) polypyridyl complexes

    NASA Astrophysics Data System (ADS)

    Huang, Kewei; Saha, Avishek; Dirian, Konstantin; Jiang, Chengmin; Chu, Pin-Lei E.; Tour, James M.; Guldi, Dirk M.; Martí, Angel A.

    2016-07-01

    Cationic ruthenium(ii) polypyridyl complexes with appended pyrene groups have been synthesized and used to disperse single-walled carbon nanotubes (SWCNT) in aqueous solutions. To this end, planar pyrene groups enable association by means of π-stacking onto carbon nanotubes and, in turn, the attachment of the cationic ruthenium complexes. Importantly, the ionic nature of the ruthenium complexes allows the formation of stable dispersions featuring individualized SWCNTs in water as confirmed in a number of spectroscopic and microscopic assays. In addition, steady-state photoluminescence spectroscopy was used to probe the excited state interactions between the ruthenium complexes and SWCNTs. These studies show that the photoluminescence of both, that is, of the ruthenium complexes and of SWCNTs, are quenched when they interact with each other. Pump-probe transient absorption experiments were performed to shed light onto the nature of the photoluminescence quenching, showing carbon nanotube-based bands with picosecond lifetimes, but no new bands which could be unambigously assigned to photoinduced charge transfer process. Thus, from the spectroscopic data, we conclude that quenching of the photoluminescence of the ruthenium complexes is due to energy transfer to proximal SWCNTs.Cationic ruthenium(ii) polypyridyl complexes with appended pyrene groups have been synthesized and used to disperse single-walled carbon nanotubes (SWCNT) in aqueous solutions. To this end, planar pyrene groups enable association by means of π-stacking onto carbon nanotubes and, in turn, the attachment of the cationic ruthenium complexes. Importantly, the ionic nature of the ruthenium complexes allows the formation of stable dispersions featuring individualized SWCNTs in water as confirmed in a number of spectroscopic and microscopic assays. In addition, steady-state photoluminescence spectroscopy was used to probe the excited state interactions between the ruthenium complexes and SWCNTs

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

    NASA Astrophysics Data System (ADS)

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

    2016-05-01

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

  3. Mechanisms of enhanced total organic carbon elimination from oxalic acid solutions by electro-peroxone process.

    PubMed

    Wang, Huijiao; Yuan, Shi; Zhan, Juhong; Wang, Yujue; Yu, Gang; Deng, Shubo; Huang, Jun; Wang, Bin

    2015-09-01

    Electro-peroxone (E-peroxone) is a novel electrocatalytic ozonation process that combines ozonation and electrolysis process to enhance pollutant degradation during water and wastewater treatment. This enhancement has been mainly attributed to several mechanisms that increase O3 transformation to ·OH in the E-peroxone system, e.g., electro-generation of H2O2 from O2 at a carbon-based cathode and its subsequent peroxone reaction with O3 to ·OH, electro-reduction of O3 to ·OH at the cathode, and O3 decomposition to ·OH at high local pH near the cathode. To get more insight how these mechanisms contribute respectively to the enhancement, this study investigated total organic carbon (TOC) elimination from oxalic acid (OA) solutions by the E-peroxone process. Results show that the E-peroxone process significantly increased TOC elimination rate by 10.2-12.5 times compared with the linear addition of the individual rates of corresponding ozonation and electrolysis process. Kinetic analyses reveal that the electrochemically-driven peroxone reaction is the most important mechanism for the enhanced TOC elimination rate, while the other mechanisms contribute minor to the enhancement by a factor of 1.6-2.5. The results indicate that proper selection of electrodes that can effectively produce H2O2 at the cathode is critical to maximize TOC elimination in the E-peroxone process. PMID:25989593

  4. Adsorption of bisphenol A from aqueous solution onto activated carbons with different modification treatments.

    PubMed

    Liu, Guifang; Ma, Jun; Li, Xuchun; Qin, Qingdong

    2009-05-30

    Two commercial carbons (W20 and F20) had been selectively modified with nitric acid and thermal treatment under a flow of N(2) in present study to adsorb bisphenol A from aqueous solution. The results indicated that the experimental data were well described with pseudo-second-order kinetic model. W20 and its thermal modified sample (W20N) represented a better adsorption capacity, and the equilibrium adsorption amounts reached 382.12 and 432.34 mg/g, respectively. Further, effects of temperature, pH and ionic strength on bisphenol A adsorption onto W20 and W20N had been examined. It was found that the adsorbed amount of bisphenol A decreased with the increase of temperature from 288 to 318 K and changed little with the increase of pH from 5.0 to 9.0. At pH 11.0, the two activated carbons represented the weakest adsorption capacity. The adsorption capacities of bisphenol A onto W20 and W20N first decreased and then increased with the increasing of ionic strength. PMID:18977073

  5. Salt Solutions in Carbon Nanotubes: The Role of Cation- π Interactions

    NASA Astrophysics Data System (ADS)

    Pham, Tuan Anh; Mortuza, Golam; Wood, Brandon; Lau, Edmond; Ogitsu, Tadashi; Buchsbaum, Steven; Siwy, Zuzanna; Fornasiero, Francesco; Schwegler, Eric

    Understanding the structure of aqueous electrolytes at interfaces is essential for predicting and optimizing device performances for a wide variety of emerging energy and environmental technologies. In this work, we investigate the structure of two common salt solutions, NaCl and KCl, at a hydrophobic interface within narrow carbon nanotubes (CNTs). Using a combination of first-principles and classical molecular dynamics simulations, we find that the solvation structure of the cations in the CNTs can deviate substantially from the conventional weakly interacting hydrophobic picture. Instead, interactions between solvated ions and the π-orbitals of the CNTs are found to play a critically important role, with the ion solvation structure ultimately determined by a subtle interplay between cation- π interactions and the intrinsic flexibility of the solvation shell. In the case of K+, these effects result in an unusually strong propensity to partially desolvate and reside closer to the carbon wall than either Na+ and Cl-, in sharp contrast to the known ion ordering at the water-vapor interface. This work was performed under the auspices of the U.S. Department of Energy by LLNL under Contract DE-AC52-07NA27344.

  6. Electrodeposition of tantalum on carbon black in non-aqueous solution and its electrocatalytic properties.

    PubMed

    Jo, Ara; Lee, Youngmi; Lee, Chongmok

    2016-08-24

    In this work, we synthesized tantalum (Ta) nanoclusters on carbon black (Ta/CB) via simple electrodeposition in non-aqueous solvent, acetonitrile (ACN) at ambient temperature. Transmission electron microscopy (TEM) images showed that the electrodeposited Ta nanoclusters consisted of tiny Ta nanoparticles. X-ray photoelectron spectroscopy (XPS) result represented that the outermost Ta formed the native oxide on Ta/CB due to its ambient exposure to air. Electrochemical catalytic properties of prepared Ta/CB on glassy carbon electrode (Ta/CB/GC) were investigated toward reductions of oxygen and hydrogen peroxide, and oxidations of ascorbic acid and dopamine. For oxygen reduction reaction (ORR) in acid, Ta/CB/GC represented a decent electrocatalytic performance which was better or comparable to bare Pt. The operational stability in acidic condition was maintained up to 500 repetitive potential cycles presumably due to the protective native Ta oxide layer. Ta/CB/GC also showed high amperometric sensitivity (4.5 (±0.16) mA mM(-1) cm(-2), n = 5) for reduction of hydrogen peroxide in 0.1 M phosphate buffer solution (PBS, pH 7.4). In addition, Ta/CB/GC was demonstrated for the possibility of simultaneous detection of ascorbic acid and dopamine using differential pulse voltammetry (DPV). PMID:27496997

  7. Effect of carbon nanofiber surface functional groups on oxygen reduction in alkaline solution

    NASA Astrophysics Data System (ADS)

    Zhong, Ren-Sheng; Qin, Yuan-Hang; Niu, Dong-Fang; Tian, Jing-Wei; Zhang, Xin-Sheng; Zhou, Xin-Gui; Sun, Shi-Gang; Yuan, Wei-Kang

    2013-03-01

    Carbon nanofibers (CNFs) with different content of surface functional groups which are carboxyl groups (CNF-OX), carbonyl groups (CNF-CO) and hydroxyl groups (CNF-OH) and nitrogen-containing groups (CNF-ON) are synthesized, and their electrocatalytic activities toward oxygen reduction reaction (ORR) in alkaline solution are investigated. The result of X-ray photoelectron spectroscopy (XPS) characterization indicates that a higher concentration of carboxyl groups, carbonyl groups and hydroxyl groups are imported onto the CNF-OX, CNF-CO and CNF-OH, respectively. Cyclic voltammetry shows that both the oxygen- and nitrogen-containing groups can improve the electrocatalytic activity of CNFs for ORR. The CNF-ON/GC electrode, which has nitrogen-containing groups, exhibits the highest current density of ORR. Rotating disk electrode (RDE) characterization shows that the oxygen reduction on CNF-ON/GC electrode proceeds almost entirely through the four-electron reduction pathway, the CNF-OX/GC, CNF-CO/GC and CNF-OH/GC electrodes proceed a two-electron reduction pathway at low potentials (-0.2 V to -0.6 V) followed by a gradual four-electron reduction pathway at more negative potentials, while the untreated carbon nanofiber (CNF-P/GC) electrode proceeds predominantly by a two-electron reduction pathway within the whole range of potential studied.

  8. Titanium Implant Osseointegration Problems with Alternate Solutions Using Epoxy/Carbon-Fiber-Reinforced Composite

    PubMed Central

    Petersen, Richard C.

    2014-01-01

    The aim of the article is to present recent developments in material research with bisphenyl-polymer/carbon-fiber-reinforced composite that have produced highly influential results toward improving upon current titanium bone implant clinical osseointegration success. Titanium is now the standard intra-oral tooth root/bone implant material with biocompatible interface relationships that confer potential osseointegration. Titanium produces a TiO2 oxide surface layer reactively that can provide chemical bonding through various electron interactions as a possible explanation for biocompatibility. Nevertheless, titanium alloy implants produce corrosion particles and fail by mechanisms generally related to surface interaction on bone to promote an inflammation with fibrous aseptic loosening or infection that can require implant removal. Further, lowered oxygen concentrations from poor vasculature at a foreign metal surface interface promote a build-up of host-cell-related electrons as free radicals and proton acid that can encourage infection and inflammation to greatly influence implant failure. To provide improved osseointegration many different coating processes and alternate polymer matrix composite (PMC) solutions have been considered that supply new designing potential to possibly overcome problems with titanium bone implants. Now for important consideration, PMCs have decisive biofunctional fabrication possibilities while maintaining mechanical properties from addition of high-strengthening varied fiber-reinforcement and complex fillers/additives to include hydroxyapatite or antimicrobial incorporation through thermoset polymers that cure at low temperatures. Topics/issues reviewed in this manuscript include titanium corrosion, implant infection, coatings and the new epoxy/carbon-fiber implant results discussing osseointegration with biocompatibility related to nonpolar molecular attractions with secondary bonding, carbon fiber in vivo properties, electrical

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

    PubMed

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

    2016-05-21

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

  10. User-oriented batch reactor solutions to the homogeneous surface diffusion model for different activated carbon dosages.

    PubMed

    Zhang, Qiong; Crittenden, John; Hristovski, Kiril; Hand, David; Westerhoff, Paul

    2009-04-01

    This paper presents a simplified approach and user-oriented solutions to the homogeneous surface diffusion model (HSDM) equations for determining the surface diffusivity using a batch reactor system. Once the surface diffusivity is known, this model could also be used to estimate the performance of activated carbon (AC) applications as a function of contact time. In addition, fixed-bed performance can be predicted using the user-oriented solutions to the HSDM for fixed beds. The step-by-step procedure for determining surface diffusion coefficients of an activated carbon adsorber, which was initially developed by Hand, Crittenden and Thacker in 1983 for a carbon dose where C(equilibrium)/C(0)=0.5, is modified to allow calculations for different carbon dosages. This modification provides solutions to the HSDM equations for different activated carbon dosages. The solutions to the HSDM framework are provided as simplified algebraic equations suitable for quick and easy estimations of D(S). The excel spread sheet is provided in the supplemental information and a detailed example is discussed. PMID:19249812

  11. Elution of zinc in dust discharged from electric arc furnace in carbonic acid solution

    NASA Astrophysics Data System (ADS)

    Yokoyama, S.; Sasaki, T.; Sasano, J.; Izaki, M.

    2012-03-01

    The dust discharged from an electric arc furnace (EAF) is a valuable resource of zinc. As a fundamental study of extraction of zinc, iron and chlorine in the EAF dust, the elution behavior of them in carbonic acid solution was studied. The influence of the weight of the EAF dust on the elution behavior was examined in this study. Experiment was carried out putting the EAF dust from 1 g to 200 g in weight into 1 L of water that was introduced by CO2. Generally, the pH in the aqueous solution increased with an increase in weight of the additive EAF dust. Maximums of the eluted concentrations of zinc and chloride ion increased with an increase in the weight of the additive EAF dust whereas the extraction ratios of both of them decreased with an increase in the weight of the additive EAF dust. Iron in the EAF dust remained in the dust without elution. The limit of extraction of zinc from the EAF dust to water was given by the solubilities of ZnFe2O4 and ZnO expressed by eq. (6) and eq. (9) respectively.

  12. Removal of methylene blue from aqueous solution by wood millet carbon optimization using response surface methodology

    NASA Astrophysics Data System (ADS)

    Ghaedi, Mehrorang; Kokhdan, Syamak Nasiri

    2015-02-01

    The use of cheep, non-toxic, safe and easily available adsorbent are efficient and recommended material and alternative to the current expensive substance for pollutant removal from wastewater. The activated carbon prepared from wood waste of local tree (millet) extensively was applied for quantitative removal of methylene blue (MB), while simply. It was used to re-used after heating and washing with alkaline solution of ethanol. This new adsorbent was characterized by using BET surface area measurement, FT-IR, pH determination at zero point of charge (pHZPC) and Boehm titration method. Response surface methodology (RSM) by at least the number of experiments main and interaction of experimental conditions such as pH of solution, contact time, initial dye concentration and adsorbent dosage was optimized and set as pH 7, contact time 18 min, initial dye concentration 20 ppm and 0.2 g of adsorbent. It was found that variable such as pH and amount of adsorbent as solely or combination effects seriously affect the removal percentage. The fitting experimental data with conventional models reveal the applicability of isotherm models Langmuir model for their well presentation and description and Kinetic real rate of adsorption at most conditions efficiently can be represented pseudo-second order, and intra-particle diffusion. It novel material is good candidate for removal of huge amount of MB (20 ppm) in short time (18 min) by consumption of small amount (0.2 g).

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

    PubMed

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

    2010-05-15

    Carbonate hydroxyapatite (CHAP) synthesized from eggshell waste was used for removing lead ion from aqueous solutions. The effects of pH, contact time and initial concentration were studied in batch experiments. The maximum uptake of lead ion was obtained at pH 6.0. Adsorption equilibrium was established by 60 min. The pseudo-first order, pseudo-second order and intraparticle diffusion kinetic models were applied to study the kinetics of the sorption processes. The pseudo-second order kinetic model provided the best correlation (R(2)>0.9991) of the used experimental data compared to the pseudo-first order and intraparticle diffusion kinetic models. The adsorption of lead ion by CHAP increased as the initial concentration of lead ion increased in the medium. The maximum lead ion adsorbed was found to be 101 mg g(-1). It was found that the adsorption of Pb(II) on CHAP was correlated well (R(2)=0.9995) with the Langmuir equation as compared to Freundlich isotherm equation under the concentration range studied. This study indicated that CHAP could be used as an efficient adsorbent for removal of lead ion from aqueous solution. PMID:20042291

  14. Adsorption and desorption of dissolved organic matter by carbon nanotubes: Effects of solution chemistry.

    PubMed

    Engel, Maya; Chefetz, Benny

    2016-06-01

    Increasing use of carbon nanotubes (CNTs) has led to their introduction into the environment where they can interact with dissolved organic matter (DOM). This study focuses on solution chemistry effects on DOM adsorption/desorption processes by single-walled CNTs (SWCNTs). Our data show that DOM adsorption is controlled by the attachment of DOM molecules to the SWCNTs, and that the initial adsorption rate is dependent on solution parameters. Adsorbed amount of DOM at high ionic strength was limited, possibly due to alterations in SWCNT bundling. Desorption of DOM performed at low pH resulted in additional DOM adsorption, whereas at high pH, adsorbed DOM amount decreased. The extent of desorption conducted at increased ionic strength was dependent on pre-adsorbed DOM concentration: low DOM loading stimulated additional adsorption of DOM, whereas high DOM loading facilitated release of adsorbed DOM. Elevated ionic strength and increased adsorbed amount of DOM reduced the oxidation temperature of the SWCNTs, suggesting that changes in the assembly of the SWCNTs had occurred. Moreover, DOM-coated SWCNTs at increased ionic strength provided fewer sites for atrazine adsorption. This study enhances our understanding of DOM-SWCNT interactions in aqueous systems influenced by rapid changes in salinity, and facilitates potential use of SWCNTs in water-purification technologies. PMID:26878603

  15. Nature of Glycine and Its α-Carbon Radical in Aqueous Solution: A Theoretical Investigation.

    PubMed

    Wood, Geoffrey P F; Gordon, Mark S; Radom, Leo; Smith, David M

    2008-10-14

    Quantum chemistry calculations and classical molecular dynamics simulations have been used to examine the equilibria in solution between the neutral and zwitterionic forms of glycine and also of the glycyl radical. The established preference (by 30 kJ mol(-1)) for the zwitterion of glycine was confirmed by both the quantum chemical calculations and the classical molecular dynamics simulations. The best agreement with experiment was derived from thermodynamic integration calculations of explicitly solvated systems, which gives a free energy difference of 36.6 ± 0.6 kJ mol(-1). In contrast, for the glycyl radical in solution, the neutral form is preferred, with a calculated free energy difference of 54.8 ± 0.6 kJ mol(-1). A detailed analysis of the microsolvation environments of each species was carried out by evaluating radial distribution functions and hydrogen bonding patterns. This analysis provides evidence that the change in preference between glycine and glycyl radical is due to the inherent gas-phase stability of the neutral α-carbon radical rather than to any significant difference in the solvation behavior of the constituent species. PMID:26620181

  16. Direct Assembly of Modified Proteins on Carbon Nanotubes in an Aqueous Solution

    NASA Technical Reports Server (NTRS)

    Kim, Jae-Woo; Lillehei, Peter T.; Park, Cheol; Harrison, Joycelyn S.

    2007-01-01

    Carbon nanotubes (CNTs) have superior mechanical and electrical properties that have opened up many potential applications. However, poor dispersibility and solubility, due to the substantial van der Waals attraction between tubes, have prevented the use of CNTs in practical applications, especially biotechnology applications. Effective dispersion of CNTs into small bundles or individual tubes in solvents is crucial to ensure homogeneous properties and enable practical applications. In addition to dispersion of CNTs into a solvent, the selection of appropriate solvent, which is compatible with a desired matrix, is an important factor to improve the mechanical, thermal, optical, and electrical properties of CNT-based fibers and composites. In particular, dispersion of CNTs into an aqueous system has been a challenge due to the hydrophobic nature of CNTs. Here we show an effective method for dispersion of both single wall CNTs (SWCNTs) and few wall CNTs (FWCNTs) in an aqueous buffer solution. We also show an assembly of cationized Pt-cored ferritins on the well dispersed CNTs in an aqueous buffer solution.

  17. Solution-processed carbon nanotube thin-film complementary static random access memory

    NASA Astrophysics Data System (ADS)

    Geier, Michael L.; McMorrow, Julian J.; Xu, Weichao; Zhu, Jian; Kim, Chris H.; Marks, Tobin J.; Hersam, Mark C.

    2015-11-01

    Over the past two decades, extensive research on single-walled carbon nanotubes (SWCNTs) has elucidated their many extraordinary properties, making them one of the most promising candidates for solution-processable, high-performance integrated circuits. In particular, advances in the enrichment of high-purity semiconducting SWCNTs have enabled recent circuit demonstrations including synchronous digital logic, flexible electronics and high-frequency applications. However, due to the stringent requirements of the transistors used in complementary metal-oxide-semiconductor (CMOS) logic as well as the absence of sufficiently stable and spatially homogeneous SWCNT thin-film transistors, the development of large-scale SWCNT CMOS integrated circuits has been limited in both complexity and functionality. Here, we demonstrate the stable and uniform electronic performance of complementary p-type and n-type SWCNT thin-film transistors by controlling adsorbed atmospheric dopants and incorporating robust encapsulation layers. Based on these complementary SWCNT thin-film transistors, we simulate, design and fabricate arrays of low-power static random access memory circuits, achieving large-scale integration for the first time based on solution-processed semiconductors.

  18. Solution-processed carbon nanotube thin-film complementary static random access memory.

    PubMed

    Geier, Michael L; McMorrow, Julian J; Xu, Weichao; Zhu, Jian; Kim, Chris H; Marks, Tobin J; Hersam, Mark C

    2015-11-01

    Over the past two decades, extensive research on single-walled carbon nanotubes (SWCNTs) has elucidated their many extraordinary properties, making them one of the most promising candidates for solution-processable, high-performance integrated circuits. In particular, advances in the enrichment of high-purity semiconducting SWCNTs have enabled recent circuit demonstrations including synchronous digital logic, flexible electronics and high-frequency applications. However, due to the stringent requirements of the transistors used in complementary metal-oxide-semiconductor (CMOS) logic as well as the absence of sufficiently stable and spatially homogeneous SWCNT thin-film transistors, the development of large-scale SWCNT CMOS integrated circuits has been limited in both complexity and functionality. Here, we demonstrate the stable and uniform electronic performance of complementary p-type and n-type SWCNT thin-film transistors by controlling adsorbed atmospheric dopants and incorporating robust encapsulation layers. Based on these complementary SWCNT thin-film transistors, we simulate, design and fabricate arrays of low-power static random access memory circuits, achieving large-scale integration for the first time based on solution-processed semiconductors. PMID:26344184

  19. Arsenic removal from aqueous solutions by adsorption onto iron oxide/activated carbon magnetic composite

    PubMed Central

    2014-01-01

    In this work the adsorption features of activated carbon and the magnetic properties of iron oxides were combined in a composite to produce magnetic adsorbent. Batch experiments were conducted to study the adsorption behavior of arsenate onto the synthetic magnetic adsorbent. The effects of initial solution pH, contact time, adsorbent dosage and co-existing anionic component on the adsorption of arsenate were investigated. The results showed that the removal percentage of arsenate could be over 95% in the conditions of adsorbent dosage 5.0 g/L, initial solution pH 3.0-8.0, and contact time 1 h. Under the experimental conditions, phosphate and silicate caused greater decrease in arsenate removal percentage among the anions, and sulfate had almost no effect on the adsorption of arsenate. Kinetics study showed that the overall adsorption rate of arsenate was illustrated by the pseudo-second-order kinetic model. The applicability of the Langmuir and Freundlich models for the arsenate adsorption data was tested. Both the models adequately describe the experimental data. Moreover, the magnetic composite adsorbent could be easily recovered from the medium by an external magnetic field. It can therefore be potentially applied for the treatment of water contaminated by arsenate. PMID:24602339

  20. Influence of different alcohols on the swelling behaviour of hydrogels

    NASA Astrophysics Data System (ADS)

    Althans, Daniel; Langenbach, Kai; Enders, Sabine

    2012-06-01

    The swelling equilibrium of cross-linked poly(N-isopropylacrylamide) (PNIPAAm) hydrogels in alcohol solutions as a function of temperature, alcohol concentration, kind of alcohol (C1OH-C3OH) and gel properties was investigated experimentally. Additionally, the swelling degree as a function of the alcohol concentration was modelled with the UNIQUAC-Free Volume model in combination with the Phantom Network theory. The experiments show that, in pure water, the transition temperature is between 303.15 and 308.15 K depending on the properties of the gel and hence on the polymerization conditions. The transition from a swollen to a shrunken state is caused by the polymeric network and the change of polymer chain localization. In a system with hydrogel + water + alcohol, the swelling degree decreases with increasing alcohol concentration until the shrunken state is reached and increases again by further addition of alcohol at constant temperature. With increasing carbon number of the alcohols, the transition from a swollen to a shrunken state and vice versa shifts to lower concentrations at constant temperature. The use of the UNIQUAC-Free Volume model with Phantom Network theory leads to results in good agreement with the experimental data.

  1. Analytical solution of geological carbon sequestration under constant pressure injection into a horizontal radial reservoir

    NASA Astrophysics Data System (ADS)

    Jhang, R.; Liou, T.

    2013-12-01

    Carbon capture and sequestration (CCS) is believed to be an economically feasible technology to mitigate global warming by capturing carbon dioxide (CO2), the major component of greenhouse gases, from the atmosphere and injecting it into deep geological formations.Several mechanisms can help trap CO2 in the pore space of a geological reservoir, stratigraphic and structural trapping, hydrodynamic trapping, and geochemical trapping.Besides these trapping mechanisms, another important issue that deserves careful attention is the risk of CO2 leakage. The common ';constant injection rate' scenario may induce high pressure buildup that will endanger the mechanical integrity as well as the sealing capability of the cap rock. Instead of injecting CO2 at a constant mass rate, CO2 can be injected into the reservoir by fixing the pressure (usually the bottom-hole pressure) in the injection borehole. By doing so, the inevitable pressure buildup associated with the constant injection scheme can be completely eliminated in the constant pressure injection scheme. In this paper, a semi-analytical solution for CO2 injection with constant pressure was developed. For simplicity, structural and geochemical trapping mechanisms were not considered. Therefore, a horizontal reservoir with infinite radial extent was considered. Prior to injection, the reservoir is fully saturated with the formation brine. It is assumed that CO2 does not mix with brine such that a sharp interface is formed once CO2 invades the brine-saturated pores. Because of the density difference between CO2 and brine, CO2 resides above the interface. Additional assumptions were also made when building up the brine and CO2 mass balance equations: (1) both of the fluids and the geological formations are incompressible, (2) capillary pressure is neglected, (3)there is no fluid flow in the vertical direction, and the horizontal flow satisfies the Darcy's law.In order to solve for the height of brine-CO2 interface, the two

  2. Comparison of Solution and Crystal Properties of Co(II)-Substituted Human Carbonic Anhydrase II

    PubMed Central

    Avvaru, Balendu Sankara; Arenas, Daniel J.; Tu, Chingkuang; Tanner, D. B.; McKenna, Robert; Silverman, David N.

    2010-01-01

    The visible absorption of crystals of Co(II)-substituted human carbonic anhydrase II (Co(II)-HCA II) were measured over a pH range of 6.0 to 11.0 giving an estimate of pKa 8.4 for the ionization of the metal-bound water in the crystal. This is higher by about 1.2 pKa units than the pKa near 7.2 for Co(II)-CA II in solution. This effect is attributed to a nonspecific ionic strength effect of 1.4 M citrate in the precipitant solution used in the crystal growth. A pKa of 8.3 for the aqueous ligand of the cobalt was measured for Co(II)-HCA II in solution containing 0.8 M citrate. Citrate is not an inhibitor of the catalytic activity of Co(II)-HCA II and was not observed in crystal structures. The X-ray structures at 1.5–1.6Å resolution of Co(II)-HCA II were determined for crystals prepared at pH 6.0, 8.5 and 11.0 and revealed no conformational changes of amino-acid side chains as a result of the use of citrate. However, the studies of Co(II)-HCA II did reveal a change in metal coordination from tetrahedral at pH 11 to a coordination consistent with a mixed population of both tetrahedral and penta-coordinate at pH 8.5 to an octahedral geometry characteristic of the oxidized enzyme Co(III)-HCA II at pH 6.0. PMID:20637176

  3. A Search for Interstellar Carbon-chain Alcohol HC4OH in Star-forming Region l1527 and Dark Cloud TMC-1

    NASA Astrophysics Data System (ADS)

    Araki, Mitsunori; Takano, Shuro; Yamabe, Hiromichi; Koshikawa, Naohiro; Tsukiyama, Koichi; Nakane, Aya; Okabayashi, Toshiaki; Kunimatsu, Arisa; Kuze, Nobuhiko

    2012-01-01

    We report a sensitive search for the rotational transitions of the carbon-chain alcohol HC4OH in the frequency range 21.2-46.7 GHz in the star-forming region L1527 and the dark cloud TMC-1. The motivation was laboratory detection of HC4OH by microwave spectroscopy. Despite achieving rms noise levels of several millikelvin in the antenna temperature using the 45 m telescope at Nobeyama Radio Observatory, the detection was not successful, leading to 3σ upper limits corresponding to the column densities of 2.0 × 1012 and 5.6 × 1012 cm-2 in L1527 and TMC-1, respectively. These upper limits indicate that [HC4OH]/[HC5N] ratios are less than 0.3 and 0.1 in L1527 and TMC-1, respectively, where HC5N is an HC4-chain cyanide and HC4OH is a hydroxide. These ratios suggest that the cyano carbon-chain molecule dominates the hydroxyl carbon-chain molecule in L1527 and TMC-1. This is contrary to the case of saturated compounds in hot cores, e.g., CH3OH and CH3CN, and can be a chemical feature of carbon-chain molecules in L1527 and TMC-1. In addition, the column densities of the "unsubstituted" carbon-chain molecule C4H and the sulfur-bearing molecules SO and HCS+ were determined from detected lines in L1527.

  4. Experimental and Theoretical Studies of the Acid-Catalyzed Conversion of Furfuryl Alcohol to Levulinic Acid in Aqueous Solution

    SciTech Connect

    Gonzalez Maldonado, Gretchen M.; Assary, Rajeev S.; Dumesic, James A.; Curtiss, Larry A.

    2012-02-14

    The conversion of furfuryl alcohol (FAL) to levulinic acid over Amberlyst TM 15 in aqueous media was investigated using a combination of liquid chromatography-mass spectrometry (LC-MS) measurements, isotopic labeling studies, nuclear magnetic resonance (NMR) spectroscopy, and ab initio quantum chemical calculations using the G4MP2 method. The results of these combined studies showed that one of the major reaction pathways takes place via a geminal diol species (4,5,5- trihydroxypentan-2-one, denoted as intermediate A), formed by the addition of two water molecules to FAL, where two of the oxygen atoms from FAL are retained. This geminal diol species can also be produced from another intermediate found to be a dimer-like species, denoted as intermediate B. This dimer-like species is formed at the early stages of reaction, and it can also be converted to intermediate A, indicating that intermediate B is the product of the reaction of FAL with another early intermediate. Quantum chemical calculations suggested this to be a protonated acyclic species. Reaction of this early intermediate with water produces intermediate A, while reaction with FAL produces intermediate B.

  5. Formation of cerussite and hydrocerussite during adsorption of lead from aqueous solution on oxidized carbons by cold oxygen plasma

    NASA Astrophysics Data System (ADS)

    De Velasco Maldonado, Paola S.; Hernández-Montoya, Virginia; Concheso, A.; Montes-Morán, Miguel A.

    2016-11-01

    A new procedure of elimination of Pb2+ from aqueous solution using carbon adsorbents, in which high amounts of cerussite and hydrocerussite are deposited on the carbon surfaces, is reported. The procedure includes the preparation of carbons from selected lignocellulosic wastes (pecan nut shells and peach stones) by single carbonization and further oxidation with cold oxygen plasma. The materials prior and after the oxidation treatment were characterized using elemental analysis, FT-IR spectroscopy, SEM/EDX analysis, adsorption of N2 at -196 °C and X-ray photoelectron spectroscopy. The adsorption of Pb2+ was carried out in batch systems under constant agitation. The formation of cerussite and hydrocerussite on the spent carbon surfaces was confirmed by XRD, SEM/EDX and FT-IR. A Pb2+ removal mechanism is proposed in which a co-precipitation of lead nitrate and calcium carbonate would render the formation of the lead carbonates. In such mechanism, the occurrence of CaCO3 on the surface of the adsorbents plays a crucial role. The presence of calcium carbonate on the precursors is understood on the basis of the thermal evolution of calcium oxalate originally present in the biomass. The oxygen plasma treatment helps to expose the calcium carbonate nanocrystals thus improving dramatically the removal capacity of Pb2+. Accordingly, retention capacities as high as 63 mg of Pb2+ per gram of adsorbent have been attained.

  6. Development and distribution of bed-parallel compaction bands and pressure solution seams in carbonates (Bolognano Formation, Majella Mountain, Italy)

    NASA Astrophysics Data System (ADS)

    Rustichelli, Andrea; Tondi, Emanuele; Agosta, Fabrizio; Cilona, Antonino; Giorgioni, Maurizio

    2012-04-01

    The Oligo-Miocene carbonates pertaining to the Bolognano Formation, cropping out at the Majella Mountain, Italy, are diffusely crosscut by bed-parallel structural elements such as compaction bands and pressure solution seams. These bed-parallel structural elements formed under a vertical loading, during the progressive burial of the carbonates. The present work focuses on the control exerted on their development and distribution by compositional, sedimentological and pore network characteristics of the studied carbonates. The main results are consistent with the following statements: (i) bed-parallel compaction bands developed only within the poorly cemented, porous grainstones (2D porosity > 10%; 3D porosity > 15%); (ii) distribution of these bands was strongly controlled by both sorting and sphericity of the carbonate grains, as well as by the amount of intergranular macroporosity; (iii) bed-parallel pressure solution seams formed, mainly, within the fine-grained packstones, which are characterized by small amounts of clayish matrix (2-4% of total rock volume), and well-sorted, spherical carbonate grains. Considering the impact that burial-related, bed-parallel structures may have on fluid flow, the results provided in this contribution can help the management of subsurface geofluids, and overall prediction of carbonate reservoir quality, by mapping/simulating/assessing carbonate facies.

  7. Spectroscopic and electrochemical studies of selected lanthanides and actinides in concentrated aqueous carbonate and carbonate-hydroxide solutions and in molten dimethyl sulfone

    SciTech Connect

    Varlashkin, P.G.

    1985-03-01

    Electrochemical and spectroscopic studies of neptunium, plutonium, americium, californium, and terbium in concentrated aqueous carbonate and carbonate-hydroxide solutions have been carried out. Changes in the absorption spectra of Np(VII), Np(V), Pu(VI), Pu(V), Am(VI), and Am(V) in concentrated Na/sub 2/CO/sub 3/ solution and in the formal potentials of the Np(VI)/Np(V) and Pu(VI)/Pu(V) couples as a function of pH were observed. Heptavalent neptunium in concentrated Na/sub 2/CO/sub 3/ solution could only be producted at pH values close to or greater than 14. Plutonium(VII) in 2 M Na/sub 2/CO/sub 3/ solution could only be produced at hydroxide ion concentrations in excess of about 2.5 M. The complexation of Np(VII) and Pu(VII) in Na/sub 2/CO/sub 3/-NaOH solution seems to be mainly by hydroxide ions. Neptunium(IV) and plutonium(IV) are insoluble in Na/sub 2/CO/sub 3/ solution above ca. pH 11-12. Neptunium(III) in carbonate solution is rapidly oxidized by water to Np(IV). Plutonium(III) is insoluble in Na/sub 2/CO/sub 3/ solution. In K/sub 2/CO/sub 3/ solution Pu(III) is stable to oxidation by water but is very sensitive to air oxidation. The redox properties of Cf(III) in Na/sub 2/CO/sub 3/ and K/sub 2/CO/sub 3/ solutions at pH values from 8 to 14 were investigated. The oxidation of terbium(III) in K/sub 2/CO/sub 3/-KOH solution was studied. Spectroscopic and electrochemical studies of cerium, samarium, europium, ytterbium, uranium, neptunium, plutonium, and americium in molten dimethyl sulfone (DMSO/sub 2/) at 400 K were performed. Differences in the DMSO/sub 2/ solution absorption spectra of trivalent Sm, Eu, and Yb and divalent Eu compared with those in aqueous solution were observed. Complexation effects on the spectra of Ce(III), Ce(IV), U(VI), Np(VI), Pu(VI), and Am(VI) are more noticeable in poorly coordinating DMSO/sub 2/ than they are in water. 123 references, 54 figures, 11 tables.

  8. Self-assembly of fluorescent carbon dots in a N,N-dimethylmethanamide solution via Schiff base reaction

    NASA Astrophysics Data System (ADS)

    Hu, Shengliang; Ding, Yanli; Chang, Qing; Trinchi, Adrian; Lin, Kui; Yang, Jinlong; Liu, Jun

    2015-02-01

    The transition from nanoparticles suspended in aqueous solutions into solid fluorescent structures is developed for application in solid functional devices. The presented approach enables the organization of carbon dots into rod-like shapes that can still be re-dispersed into aqueous solution. Schiff bases forming at the surface of carbon dots not only protect their surface states, but also provide sites for tethering to other carbon dots. As a consequence, the large assemblies of CDs can come together to form regular, well ordered structures whilst still maintaining their photoluminescence properties. This opens up enormous possibilities for device manufacture, as these self-assemblies could be grown or grafted onto templates forming regular structures, and find innumerable applications ranging from optoelectronic devices, light harvesting to artificial photosynthesis.The transition from nanoparticles suspended in aqueous solutions into solid fluorescent structures is developed for application in solid functional devices. The presented approach enables the organization of carbon dots into rod-like shapes that can still be re-dispersed into aqueous solution. Schiff bases forming at the surface of carbon dots not only protect their surface states, but also provide sites for tethering to other carbon dots. As a consequence, the large assemblies of CDs can come together to form regular, well ordered structures whilst still maintaining their photoluminescence properties. This opens up enormous possibilities for device manufacture, as these self-assemblies could be grown or grafted onto templates forming regular structures, and find innumerable applications ranging from optoelectronic devices, light harvesting to artificial photosynthesis. Electronic supplementary information (ESI) available: Experimental details and more characterization of carbon dot assemblies. See DOI: 10.1039/c4nr07119k

  9. Ca-Rich Carbonate Melts: A Regular-Solution Model, with Applications to Carbonatite Magma + Vapor Equilibria and Carbonate Lavas on Venus

    NASA Technical Reports Server (NTRS)

    Treiman, Allan H.

    1995-01-01

    A thermochemical model of the activities of species in carbonate-rich melts would be useful in quantifying chemical equilibria between carbonatite magmas and vapors and in extrapolating liquidus equilibria to unexplored PTX. A regular-solution model of Ca-rich carbonate melts is developed here, using the fact that they are ionic liquids, and can be treated (to a first approximation) as interpenetrating regular solutions of cations and of anions. Thermochemical data on systems of alkali metal cations with carbonate and other anions are drawn from the literature; data on systems with alkaline earth (and other) cations and carbonate (and other) anions are derived here from liquidus phase equilibria. The model is validated in that all available data (at 1 kbar) are consistent with single values for the melting temperature and heat of fusion for calcite, and all liquidi are consistent with the liquids acting as regular solutions. At 1 kbar, the metastable congruent melting temperature of calcite (CaCO3) is inferred to be 1596 K, with (Delta)bar-H(sub fus)(calcite) = 31.5 +/- 1 kJ/mol. Regular solution interaction parameters (W) for Ca(2+) and alkali metal cations are in the range -3 to -12 kJ/sq mol; W for Ca(2+)-Ba(2+) is approximately -11 kJ/sq mol; W for Ca(2+)-Mg(2+) is approximately -40 kJ/sq mol, and W for Ca(2+)-La(3+) is approximately +85 kJ/sq mol. Solutions of carbonate and most anions (including OH(-), F(-), and SO4(2-)) are nearly ideal, with W between 0(ideal) and -2.5 kJ/sq mol. The interaction of carbonate and phosphate ions is strongly nonideal, which is consistent with the suggestion of carbonate-phosphate liquid immiscibility. Interaction of carbonate and sulfide ions is also nonideal and suggestive of carbonate-sulfide liquid immiscibility. Solution of H2O, for all but the most H2O-rich compositions, can be modeled as a disproportionation to hydronium (H3O(+)) and hydroxyl (OH(-)) ions with W for Ca(2+)-H3O(+) (approximately) equals 33 kJ/sq mol. The

  10. Adsorptive removal of Zn(II) ion from aqueous solution using rice husk-based activated carbon

    NASA Astrophysics Data System (ADS)

    Taha, Mohd F.; Ibrahim, Muhammad H. C.; Shaharun, Maizatul S.; Chong, F. K.

    2012-09-01

    The study of rice husk-based activated carbon as a potential low-cost adsorbent for the removal of Zn(II) ion from aqueous solution was investigated. Rice husk, an agricultural waste, is a good alternative source for cheap precursor of activated carbon due to its abundance and constant availability. In this work, rice husk-based activated carbon was prepared via chemical treatment using NaOH as an activation agent prior the carbonization process. Three samples, i.e. raw rice husk, rice husk treated with NaOH and rice husk-based activated carbon carbonized at 650°C, were analyzed for their morphological characteristics using field-emission scanning electron microscope/energy dispersive X-ray (FESEM/EDX). Other analyses were also conducted on these samples using fourier transmitter infrared spectroscopy (FTIR), CHN elemental analyzer and X-ray diffraction (XRD) for characterization study. The porous properties of rice husk-based activated carbon were determined by Brunauer-Emmett-Teller (BET) surface area analyzer, and its surface area and pore volume were found to be 255 m2/g and 0.17 cm2/g, respectively. The adsorption studies for the removal of Zn(II) ion from aqueous solution were carried out as a function of varied contact time at room temperature. The concentration of Zn(II) ion was analyzed using atomic absorption spectrophotometer (AAS). The results obtained from adsorption studies indicate the potential of rice husk as an economically promising precursor for the preparation of activated carbon for removal of Zn(II) ion from aqueous solution.

  11. Ultrasonic Velocity, Viscosity and Refractive Index Investigation on Interacting Blend Solutions of PAA (Poly Acrylic Acid) and PVA (Poly Vinyl Alcohol) in Solvent DMSO (Di methyl Sulphoxide)

    NASA Astrophysics Data System (ADS)

    Nagamani, Chakrala

    2010-11-01

    The present study provides a great insight into the major new research areas like Plasma research (which is yielding a greater understanding of the universe) and Nano Technology Research (which provides many practical uses like Drug Delivery System). The Ultrasonic Velocities, Viscosities and Refractive indices of Poly (Acrylic Acid) and Poly (Vinyl Alcohol) blends in DMSO solutions have been measured over a wide range of composition, concentration and at different temperatures. The variation of Ultrasonic Velocity, derived acoustical parameters, adiabatic compressibility, acoustic impedance, Rao number, molar compressibility and relaxation strength with composition of blend solution was found not linear. This non-linearity has been attributed to incompatibility in conformity with the earlier findings. This behavior was confirmed by Viscometric and interaction parameters studies, as well as by investigation of Refractive index studies. These investigations offer an entirely new and simple approach to the study of the compatibility of polymer blends which is in general obtained by sophisticated techniques of thermal dynamic mechanical and electron microscopic analysis.

  12. Stability of fluctuating and transient aggregates of amphiphilic solutes in aqueous binary mixtures: Studies of dimethylsulfoxide, ethanol, and tert-butyl alcohol

    NASA Astrophysics Data System (ADS)

    Banerjee, Saikat; Bagchi, Biman

    2013-10-01

    In aqueous binary mixtures, amphiphilic solutes such as dimethylsulfoxide (DMSO), ethanol, tert-butyl alcohol (TBA), etc., are known to form aggregates (or large clusters) at small to intermediate solute concentrations. These aggregates are transient in nature. Although the system remains homogeneous on macroscopic length and time scales, the microheterogeneous aggregation may profoundly affect the properties of the mixture in several distinct ways, particularly if the survival times of the aggregates are longer than density relaxation times of the binary liquid. Here we propose a theoretical scheme to quantify the lifetime and thus the stability of these microheterogeneous clusters, and apply the scheme to calculate the same for water-ethanol, water-DMSO, and water-TBA mixtures. We show that the lifetime of these clusters can range from less than a picosecond (ps) for ethanol clusters to few tens of ps for DMSO and TBA clusters. This helps explaining the absence of a strong composition dependent anomaly in water-ethanol mixtures but the presence of the same in water-DMSO and water-TBA mixtures.

  13. Stability of fluctuating and transient aggregates of amphiphilic solutes in aqueous binary mixtures: studies of dimethylsulfoxide, ethanol, and tert-butyl alcohol.

    PubMed

    Banerjee, Saikat; Bagchi, Biman

    2013-10-28

    In aqueous binary mixtures, amphiphilic solutes such as dimethylsulfoxide (DMSO), ethanol, tert-butyl alcohol (TBA), etc., are known to form aggregates (or large clusters) at small to intermediate solute concentrations. These aggregates are transient in nature. Although the system remains homogeneous on macroscopic length and time scales, the microheterogeneous aggregation may profoundly affect the properties of the mixture in several distinct ways, particularly if the survival times of the aggregates are longer than density relaxation times of the binary liquid. Here we propose a theoretical scheme to quantify the lifetime and thus the stability of these microheterogeneous clusters, and apply the scheme to calculate the same for water-ethanol, water-DMSO, and water-TBA mixtures. We show that the lifetime of these clusters can range from less than a picosecond (ps) for ethanol clusters to few tens of ps for DMSO and TBA clusters. This helps explaining the absence of a strong composition dependent anomaly in water-ethanol mixtures but the presence of the same in water-DMSO and water-TBA mixtures. PMID:24182023

  14. Alcoholic ketoacidosis

    MedlinePlus

    ... attention improves the overall outlook. How severe the alcoholism is, and the presence of liver disease or ... A.M. Editorial team. Related MedlinePlus Health Topics Alcoholism and Alcohol Abuse Browse the Encyclopedia A.D. ...

  15. Alcohol withdrawal

    MedlinePlus

    ... counseling to discuss the long-term issue of alcoholism Testing and treatment for other medical problems linked ... following organizations are good resources for information on alcoholism: Alcoholics Anonymous -- www.aa.org Al-Anon/Alateen -- ...

  16. Alcoholic neuropathy

    MedlinePlus

    ... objects in the shoes Guarding the extremities to prevent injury from pressure Alcohol must be stopped to prevent the damage from ... The only way to prevent alcoholic neuropathy is not to drink excessive amounts of alcohol.

  17. Activated carbons from potato peels: The role of activation agent and carbonization temperature of biomass on their use as sorbents for bisphenol A uptake from aqueous solutions

    NASA Astrophysics Data System (ADS)

    Arampatzidou, An; Deliyanni, Eleni A.

    2015-04-01

    Activated carbons prepared from potato peels, a solid waste by product, and activated with different activating chemicals, have been studied for the adsorption of an endocrine disruptor (Bisphenol-A) from aqueous solutions. The potato peels biomass was activated with phosphoric acid, KOH and ZnCl2. The different activating chemicals were tested in order the better activation agent to be found. The carbons were carbonized by pyrolysis, in one step procedure, at three different temperatures in order the role of the temperature of carbonization to be pointed out. The porous texture and the surface chemistry of the prepared activated carbons were characterized by Nitrogen adsorption (BET), Scanning Electron Microscope (SEM), thermal analysis (DTA) and Fourier Transform Infrared Spectroscopy (FTIR). Batch experiments were performed to investigate the effect of pH, the adsorbent dose, the initial bisphenol A concentration and temperature. Equilibrium adsorption data were analyzed by Langmuir and Freundlich isotherms. The thermodynamic parameters such as the change of enthalpy (ΔH0), entropy (ΔS0) and Gibb's free energy (ΔG0) of adsorption systems were also evaluated. The adsorption capacity calculated from the Langmuir isotherm was found to be 450 mg g-1 at an initial pH 3 at 25 °C for the phosphoric acid activated carbon, that make the activated carbon a promising adsorbent material.

  18. Relationships among folate, alcohol consumption, gene variants in one-carbon metabolism and p16INK4a methylation and expression in healthy breast tissues.

    PubMed

    Llanos, Adana A; Dumitrescu, Ramona G; Brasky, Theodore M; Liu, Zhenhua; Mason, Joel B; Marian, Catalin; Makambi, Kepher H; Spear, Scott L; Kallakury, Bhaskar V S; Freudenheim, Jo L; Shields, Peter G

    2015-01-01

    p16(INK4a) is a tumor suppressor gene, frequently hypermethylated in breast cancer; this epigenetic silencing of p16(INK4a) occurs early in carcinogenesis. The risk factors and functional consequences of p16(INK4a) methylation are unknown. Alcohol consumption, a breast cancer risk factor, impedes folate metabolism and may thereby alter gene methylation since folate plays a pivotal role in DNA methylation. In a cross-sectional study of 138 women with no history of breast cancer who underwent reduction mammoplasty, we studied breast cancer risk factors, plasma and breast folate concentrations, variation in one-carbon metabolism genes, p16(INK4a) promoter methylation and P16 protein expression. Logistic regression was used to estimate multivariable-adjusted odds ratios (OR) and 95% confidence intervals (CI). p16(INK4a) methylation was negatively correlated with P16 expression (r = -0.28; P = 0.002). Alcohol consumption was associated with lower breast folate (P = 0.03), higher p16(INK4a) promoter methylation (P = 0.007) and less P16 expression (P = 0.002). Higher breast folate concentrations were associated with lower p16(INK4a) promoter methylation (P = 0.06). Genetic variation in MTRR (rs1801394) and MTHFD1 (rs1950902) was associated with higher p16 (INK4a) promoter methylation (OR = 2.66, 95% CI: 1.11-6.42 and OR = 2.72, 95% CI: 1.12-6.66, respectively), whereas variation in TYMS (rs502396) was associated with less P16 protein expression (OR = 0.22, 95% CI: 0.05-0.99). Given that this is the first study to indicate that alcohol consumption, breast folate and variation in one-carbon metabolism genes are associated with p16(INK4a) promoter methylation and P16 protein expression in healthy tissues; these findings require replication. PMID:25344837

  19. Resistivity reduction of boron-doped multiwalled carbon nanotubes synthesized from a methanol solution containing boric acid

    NASA Astrophysics Data System (ADS)

    Ishii, Satoshi; Watanabe, Tohru; Ueda, Shinya; Tsuda, Shunsuke; Yamaguchi, Takahide; Takano, Yoshihiko

    2008-05-01

    Boron-doped multiwalled carbon nanotubes (MWNTs) were synthesized using a methanol solution of boric acid as a source material. Accurate measurements of the electrical resistivity of an individual boron-doped MWNT was performed with a four-point contact, which was fabricated using an electron beam lithography technique. The doped boron provides conduction carriers, which reduces the resistivity of the MWNT.

  20. Chemisorption of Perfluorooctanoic Acid on Powdered Activated Carbon Initiated by Persulfate in Aqueous Solution.

    PubMed

    Sun, Bo; Ma, Jun; Sedlak, David L

    2016-07-19

    Perfluorooctanoic acid (PFOA) is a perfluorocarboxylic acid that is difficult to treat by most conventional methods. As a result, it is often removed from solution by adsorption on powdered activated carbon (PAC), followed by incineration of the spent carbon. To provide a new approach for treatment, PFOA was exposed to sulfate radicals (SO4(-•)) produced by thermolysis of persulfate (S2O8(2-)) in the presence of PAC. Under acidic conditions, thermal activation of persulfate resulted in transformation of PFOA to shorter-chain-length perfluorinated compounds, as previously reported. However, when thermolysis of persulfate occurred under circumneutral pH conditions in the presence of PAC, a new removal pathway for PFOA was observed. Under these conditions, the removal of PFOA was attributable to chemisorption, a process in which PAC catalyzed persulfate decomposition and reacted with the transformation products to produce covalently bound PFOA. At PAC concentrations between 200 and 1000 mg/L and an initial PFOA concentration of 0.5 μM, covalent bonding resulted in removal of 10-40% of the PFOA. Under these conditions, the process resulted in removal of more than half of a more hydrophilic perfluoroalkyl acid (i.e., perfluorobutanoic acid, PFBA), which was greater than the amount of PFBA removed by physical adsorption on PAC. Although the high reaction temperatures (i.e., 80 °C) and relatively high doses of PAC used in this study may be impractical for drinking water treatment, this process may be applied to the treatment of these recalcitrant compounds in industrial wastewater, reverse osmosis concentrate, and other waters that contain high concentrations of PFOA and other perfluorocarboxylic acids. PMID:27336204

  1. Functionalization of Multiwalled Carbon Nanotubes by Solution Plasma Processing in Ammonia Aqueous Solution and Preparation of Composite Material with Polyamide 6

    NASA Astrophysics Data System (ADS)

    Shirafuji, Tatsuru; Noguchi, Yohei; Yamamoto, Taibou; Hieda, Junko; Saito, Nagahiro; Takai, Osamu; Tsuchimoto, Akiharu; Nojima, Kazuhiro; Okabe, Youji

    2013-12-01

    Solution plasma processing (SPP) has been performed on multiwalled carbon nanotubes (MWCNTs) in ammonia aqueous solution. The MWCNTs, which do not disperse in aqueous solution, uniformly dispersed after the SPP. Only 2 h was required to obtain 10 g of the dispersed MWCNTs, while 7 days and additional chemicals were required for 185 mg in a previous study. The X-ray photoelectron spectroscopy and Fourier-transform infrared spectroscopy of the SPP-treated MWCNTs revealed that nitrogen- and oxygen-containing groups are formed on the MWCNTs. Serious damage to the MWCNT structure was not observed in the Raman spectrum or transmission electron microscopy images of the SPP-treated MWCNTs. The composite materials prepared using polyamide 6 with the SPP-treated MWCNTs showed better tensile, bending, and impact strength than those prepared with nontreated MWCNTs.

  2. Adsorption of organic molecules at the mercury-solution interface: effect of anion specific adsorption on double layer properties. [Benzyl alcohol

    SciTech Connect

    Buckfelder, J.J. III

    1980-08-01

    Adsorption of iso-pentanol, pentanoic acid, and benzyl alcohol at the mercury-solution interface was studied in HC1O/sub 4/, H/sub 2/SO/sub 4/, NaNO/sub 3/, and NaF electrolytes. The Frumkin isotherm equation Ba = (theta/(1-theta))exp(2..cap alpha..theta) together with the implied charge vs. surface excess relation: q = (1-theta)q/sub w/ + thetaQ were used to analyze the experimental data. Linear charge vs surface excess plots were obtained for the aliphatic compounds over the entire potential region studied; for benzyl alcohol, plots were linear only at anodic potentials. The slopes of these lines agreed with those predicted by the above equation, with Q = C/sub org/(V-V/sub n/), for cathodic potentials. At potentials anodic to the electrocapillary maximum, deviations between experimental and theoretical slopes appeared. In the model proposed, the double layer consists of two parts. The layer closest to the surface is restricted to water molecules and specifically adsorbed ions. The second layer contains organic molecules exclusively; any charge necessary to balance the surface charge is considered to be in a monolayer adjacent to the organic layer. From the slope of the charge vs surface excess plots, it is possible to calculate the charge on the covered portion of the surface and then calculate the amount of specific adsorption. The relative amounts of specific adsorption are in agreement with known strengths of adsorption of the anions of the electrolyte. Capacity curves were also calculated and were in good agreement with experimental curves.

  3. Single-phase microemulsification of a complex light-nonaqueous-phase-liquid: Laboratory evaluation of several mixtures of surfactant/alcohol solutions

    SciTech Connect

    Rhue, R.D.; Rao, P.S.C.; Annable, M.D.

    1999-08-01

    A recent advance in conventional pump-and-treat technology for aquifer remediation involves the use of surfactant-alcohol mixtures that will form a clear, transparent, thermodynamically stable oil-in-water microemulsion on contact with a residual non-aqueous-phase-liquid (NAPL). An initial screening of 86 commercial-grade surfactants for aqueous solubility resulted in selection of 58 that were further tested in batch experiments to evaluate the capacity to solubilize a complex NAPL waste collected from a Superfund site (Operable Unit OU-1) at Hill AFB, UT. The selected group of 58 surfactants represented six classes of anionic, nine classes of nonionic, and one class of amphoteric surfactants. Batch studies on NAPL solubilization identified a number of surfactants suitable for use in the field demonstration phase of the project; a further criterion in surfactant selection was that the flushing solution had a viscosity <2 cp. The best surfactants among this group had HLB (hydrophilic-lipophilic balance) values between 12 and 13, and solubilized 10 to 20 g L{sup {minus}1} of the OU-1 NAPL when the surfactant concentration was 3%. Column tests using NAPL-coated glass beads showed that the more efficient surfactants could remove >90% of the NAPL after flushing with <10 pore volumes. Brij 97, an ethoxylated alcohol ether surfactant, showed a high capacity for solubilizing the OU-1 NAPL. In a column test using contaminated Hill AFB aquifer material, flushing with a mixture of 3% Brij 97 and 2.5% n-pentanol removed essentially all of the mass of nine target analytes in the NAPL after flushing with <10 pore volumes without mobilizing the NAPL or destabilizing aquifer colloids.

  4. Polymorph selection and nanocrystallite rearrangement of calcium carbonate in carboxymethyl chitosan aqueous solution: Thermodynamic and kinetic analysis

    SciTech Connect

    Zhao, Donghui; Zhu, Yingchun; Li, Fang; Ruan, Qichao; Zhang, Shengmao; Zhang, Linlin; Xu, Fangfang

    2010-01-15

    In this article, the polymorph selection of calcium carbonate has been successfully achieved in water-soluble carboxymethyl chitosan aqueous solution at different temperatures (25-95 {sup o}C). Vaterite is formed in carboxymethyl chitosan solution 25 {sup o}C accompanied with trace of calcite, whereas pure aragonite is obtained at 95 {sup o}C. Scanning electron microscopy and transmission electron microscopy analyses show that the products are formed from the recrystallization of nanometer crystallites. Thermodynamic and kinetic analyses reveal that the polymorph of calcium carbonate is controlled and selected by kinetics in various temperatures. As a heterogeneous nucleator and stabilizing agent, carboxymethyl chitosan changes the nucleation and growth of calcium carbonate from thermodynamic into kinetic control. Under kinetic limitation, the reaction rate of aragonite increases along with the elevating of temperature and surpasses the rate of vaterite above 327 K.

  5. Energetic changes in the surface of activated carbons and relationship with Ni(II) adsorption from aqueous solution

    NASA Astrophysics Data System (ADS)

    Rodríguez-Estupiñan, Paola; Giraldo, Liliana; Moreno-Piraján, Juan Carlos

    2013-12-01

    This study investigated Ni(II) ion adsorption from aqueous solution on activated carbons obtained by chemically modifying the surface with the oxidizing agents nitric acid and hydrogen peroxide (CAGoxP and CAGoxN, respectively). The activated carbons were characterized by total acidity and basicity, pH at the point of charge zero determination and IR spectroscopy. Textural parameters such as the BET area and pore volumes were evaluated by gas adsorption. The BET area of the materials was between 816 and 876 m2 g-1. Additionally, the immersion enthalpies of the activated carbons in water and benzene were determined. The experimental results on adsorption in solution were adjusted to the Langmuir and Freundlich models, obtaining values for the monolayer capacity between 29.68 and 50.97 mg g-1, which indicates that the adsorption capacity depends largely on solid surface chemistry.

  6. Calcium-magnesium carbonate solid solutions from Holocene conglomerate cements and travertines in the Coast Range of California

    USGS Publications Warehouse

    Barnes, I.; O'Neil, J.R.

    1971-01-01

    Two calcium-magnesium carbonate solid solutions form Holocene travertines and conglomerate cements in fresh water stream channels of the Coast Range of California. Calcite does not yield the {015} diffraction maximum. The {006} diffraction maximum is lacking over most of the range of composition of calcite. Calcite has compositions from CaCO3 to Ca0.5Mg0.5CO3. Dolomite yields both the {006} and {015} diffraction maxima over its entire composition range, Ca0.6Mg0.4CO3 to Ca0.5Mg0.5CO3. The Ca-Mg carbonates form in isotopic equilibrium and thermodynamic disequilibrium from dispersion of Ca2+-rich water into CO32--rich water within the alluvium. The stable isotope data suggest that all the Mg-rich carbonates are primary precipitates and not a result of Mg-substitution in precursor CaCO3. There is a correlation between ??C13 and Mg content of the carbonates which predicts a 5%. fractionation of C13 between dolomite and calcite at sedimentary temperatures. C14 is incorporated in Ca-Mg carbonates forming from C13-poor meteoric waters and C13-rich waters from Cretaceous sediments. C14 ages of the Ca-Mg carbonates are apparent, and cannot be corrected to absolute values. Solution rates of calcite decrease with increasing MgCO3 content; dolomite dissolves slower than any calcite. ?? 1971.

  7. Study of benzotriazole as corrosion inhibitors of carbon steel in chloride solution containing hydrogen sulfide using electrochemical impedance spectroscopy (EIS)

    SciTech Connect

    Solehudin, Agus; Nurdin, Isdiriayani

    2014-03-24

    Corrosion and inhibition studies on API 5LX65 carbon steel in chloride solution containing various concentrations of benzotriazole has been conducted at temperature of 70°C using Electrochemical Impedance Spectroscopy (EIS). Corroded carbon steel surface with and without inhibitor have been observed using X-ray Diffraction (XRD), Scanning Electron Microscope (SEM), and Energy Dispersive Spectroscopy (EDS). The objectives of this research are to study the performance of benzotriazole as corrosion inhibitors. The experimental results of carbon steel corrosion in 3.5% NaCl solution containing 500 mg/l H{sub 2}S at different BTAH concentrations showed that corrosion rate of carbon steel decreases with increasing of BTAH concentrations from 0 to 10 mmol/l. The inhibition efficiency of BTAH was found to be affected by its concentration. The optimum efficiency obtained of BTAH is 93% at concentration of 5 mmol/l. The result of XRD and EDS analysis reveal the iron sulfide (FeS) formation on corroded carbon steel surface without inhibitor. The EDS spectrum show the Nitrogen (N) bond on carbon steel surface inhibited by BTAH.

  8. Study of benzotriazole as corrosion inhibitors of carbon steel in chloride solution containing hydrogen sulfide using electrochemical impedance spectroscopy (EIS)

    NASA Astrophysics Data System (ADS)

    Solehudin, Agus; Nurdin, Isdiriayani

    2014-03-01

    Corrosion and inhibition studies on API 5LX65 carbon steel in chloride solution containing various concentrations of benzotriazole has been conducted at temperature of 70°C using Electrochemical Impedance Spectroscopy (EIS). Corroded carbon steel surface with and without inhibitor have been observed using X-ray Diffraction (XRD), Scanning Electron Microscope (SEM), and Energy Dispersive Spectroscopy (EDS). The objectives of this research are to study the performance of benzotriazole as corrosion inhibitors. The experimental results of carbon steel corrosion in 3.5% NaCl solution containing 500 mg/l H2S at different BTAH concentrations showed that corrosion rate of carbon steel decreases with increasing of BTAH concentrations from 0 to 10 mmol/l. The inhibition efficiency of BTAH was found to be affected by its concentration. The optimum efficiency obtained of BTAH is 93% at concentration of 5 mmol/l. The result of XRD and EDS analysis reveal the iron sulfide (FeS) formation on corroded carbon steel surface without inhibitor. The EDS spectrum show the Nitrogen (N) bond on carbon steel surface inhibited by BTAH.

  9. Prevention of Alcohol Abuse among Black Americans.

    ERIC Educational Resources Information Center

    Journal of Alcohol and Drug Education, 1992

    1992-01-01

    Originally published in "Alcohol Health and Research World," this article is report of interview with Thomas D. Watts and Roosevelt Wright, Jr., conducted to explore solutions to complex problem of prevention of alcoholism among African Americans. Introduces readers to work of two experts in area of alcohol abuse and alcoholism among African…

  10. Activated carbon prepared from yerba mate used as a novel adsorbent for removal of tannery dye from aqueous solution.

    PubMed

    Linhares, Bruno; Weber, Caroline Trevisan; Foletto, Edson Luiz; Paz, Diego Silva; Mazutti, Marcio A; Collazzo, Gabriela Carvalho

    2013-01-01

    Activated carbon prepared from yerba mate (Ilex paraguariensis) was used as adsorbent for the removal of tannery dye from aqueous solution. The activated carbon was characterized, and it showed a mesoporous texture, with surface area of 537.4 m2 g(-1). The initial dye concentration, contact time and pH influenced the adsorption capacity. The equilibrium data were in good agreement with both Langmuir and Freundlich isotherms. The adsorption kinetics of the tannery dye on activated carbon prepared from yerba mate followed a pseudo-second-order model. The adsorption process was found to be controlled by both external mass-transfer and intraparticle diffusion, but the external diffusion was the dominating process. This work highlights the potential application of activated carbon produced from yerba mate in the field of adsorption. PMID:24350496

  11. Interaction of fragmented double-stranded DNA with carbon nanotubes in aqueous solution

    NASA Astrophysics Data System (ADS)

    Gladchenko, G. O.; Karachevtsev, M. V.; Leontiev, V. S.; Valeev, V. A.; Glamazda, A. Yu.; Plokhotnichenko, A. M.; Stepanian, S. G.

    Aqueous suspensions of ultrasonically fragmented double-stranded (fds-) DNA and single-walled carbon nanotubes (SWNTs) have been investigated by UV- and IR-absorption, NIR-emission and Raman spectroscopy. According to gel-electrophoresis, the lengths of the polymer fragments were 100-500 base pairs. Analysis of IR and UV data indicates the presence of both double-stranded (ds) and single-stranded (ss)-regions in the fragments. SWNT complex with DNA was revealed by NIR-emission and Raman spectroscopy. It turned out that fds-DNA is less efficient in holding nanotubes in the aqueous solution than ss-DNA. From the UV-data, the character of the helix-coil transition is seen to be like that for fds-DNA off and on nanotube, however, DNA thermostability increased in this latter case. The effective charge density on the DNA sugar-phosphate backbone of the fds-DNA:SWNT hybrid was less than that of DNA alone. Spectroscopic data can be explained by a model in which the formation of hybrids starts due to the interaction between untwisted ss-regions of DNA and the nanotube: the strands wrap on the tube and thus create an 'anchor' for the whole polymer. The ds-part of the polymer is located close to the nanotube.

  12. Np(v) complexation with carbonate in aqueous solutions studied by spectrophotometric titration at various temperatures.

    PubMed

    Yang, Suliang; Zhao, Yaping; Tian, Guoxin

    2016-02-14

    The complexation of neptunium(v) with carbonate has been studied at temperatures from 10 to 70 °C in 0.1 M LiClO4 by spectrophotometry. Three NpO2(+)-CO3(2-) complex species, NpO2(CO3)n((2n-1)-) (n = 1, 2, 3), are identified and the stability constants are calculated by using the absorption spectra in the near-IR region collected from titrations at varying temperatures. The enthalpies and entropies are calculated with van't Hoff equations in the temperature range of 10 to 70 °C, indicating that the formation of all NpO2(+)-CO3(2-) complexes is mainly entropy driven. The structures of the NpO2(+)-CO3(2-) complex species in aqueous solutions are also reviewed. Based on the molar absorptivity of Np(v) in the near-IR region the structure of NpO2(CO3)2(3-) is re-constructed as NpO2(CO3)2(H2O)(3-)of low symmetry but not as NpO2(CO3)2(H2O)2(3-)of high symmetry as suggested in a previous study. PMID:26744184

  13. Characteristics of cesium ion sorption from aqueous solution on bentonite- and carbon nanotube-based composites.

    PubMed

    Yang, Shubin; Han, Cho; Wang, Xiangke; Nagatsu, Masaaki

    2014-06-15

    The technology development of Cs(+) capture from aqueous solution is crucial for the disposal of nuclear waste and still remains a significant challenge. Previous researches have been proven that ion exchanges with the cations and hydroxyl exchange are the main sorption mechanisms for Cs(+). Therefore, how important are the cation exchange and the hydroxyl exchange mechanisms to Cs(+) sorption? And whether can we improve the sorption capacity of the material by increasing the amount of hydroxyl groups? With these in mind, we herein designed the chitosan-grafted carbon nanotubes (CS-g-CNTs) and the chitosan-grafted bentonite (CS-g-bentonite) by plasma-induced grafting method. The interactions of Cs(+) with CNTs, bentonite, CS-g-CNTs and CS-g-bentonite composites were investigated. The sorption of Cs(+) is mainly dominated by strong cation exchange in monovalent Group I and divalent Group II. And the cation-exchange mechanism is much more effective than the hydroxyl group exchange. The effect of hydroxyl groups is dependent on the property of the matrix. We cannot improve the Cs adsorption capacity of material for Cs(+) only by increasing the amount of hydroxyl groups in any case. The spatial structure and the cation-exchange capacity of the material are important factors for choosing the sorbent for Cs(+) removal from radioactive waste water. PMID:24762700

  14. Low-cost, solution processable carbon nanotube supercapacitors and their characterization

    NASA Astrophysics Data System (ADS)

    Lehtimäki, Suvi; Tuukkanen, Sampo; Pörhönen, Juho; Moilanen, Pasi; Virtanen, Jorma; Honkanen, Mari; Lupo, Donald

    2014-06-01

    We report ecological and low-cost carbon nanotube (CNT) supercapacitors fabricated using a simple, scalable solution processing method, where the use of a highly porous and electrically conductive active material eliminates the need for a current collector. Electrodes were fabricated on a poly(ethylene terephthalate) substrate from a printable multi-wall CNT ink, where the CNTs are solubilized in water using xylan as a dispersion agent. The dispersion method facilitates a very high concentration of CNTs in the ink. Supercapacitors were assembled using a paper separator and an aqueous NaCl electrolyte and the devices were characterized with a galvanostatic discharge method defined by an industrial standard. The capacitance of the 2 cm^2 devices was 6 mF/cm^2 (2.3 F/g) and equivalent series resistance 80 Ω . Low-cost supercapacitors fabricated from safe and environmentally friendly materials have potential applications as energy storage devices in ubiquitous and autonomous intelligence as well as in disposable low-end products.

  15. Partial carbonized nanoporous resin for uptake of lead from aqueous solution.

    PubMed

    Ghiloufi, I; Al-Hobaib, A S; El Mir, L

    2015-01-01

    Four partial carbonized nanoporous resins (PCNRs), based on organic xerogel compounds, were synthesised by the sol-gel method from pyrogallol and formaldehyde mixtures in water using picric acid as catalyst. The PCNRs were prepared at different pyrolysis temperatures: T(1) = 200 °C (PF-200), T(2) = 300 °C (PF-300), T(3) = 400 °C (PF-400), or T(4) = 500 °C (PF-500). The PCNRs were characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Fourier transformed infrared spectroscopy, and nitrogen porosimetry. The obtained results show that PF-200 is more efficient for the removal of Pb(2+) from aqueous solution than the other adsorbent prepared in this study. The characteristics of lead uptake by PF-200 were explored using well-established and effective parameters including pH, contact time, initial metal ion concentration and temperature. Optimum adsorption of Pb(2+), using PF-200, was observed at pH 4.5. The Langmuir model gave a better fit than the other models, and kinetic studies revealed that the adsorption was well fitted by the pseudo second-order kinetic model and thermodynamic properties, i.e., Gibbs free energy change, enthalpy change and entropy change, showed that adsorption of Pb(2+) onto PF-200 was endothermic, spontaneous and feasible in the temperature range of 298-328 K. PMID:26360758

  16. Comparative performance of cement kiln dust and activated carbon in removal of cadmium from aqueous solutions.

    PubMed

    El-Refaey, Ahmed A

    2016-01-01

    This study compared the performance of cement kiln dust (CKD) as industrial byproduct and commercially activated carbon (AC) as adsorbent derived from agricultural waste for the removal of cadmium (Cd(2+)) from aqueous solutions. CKD and AC were characterized by Fourier transform infrared (FTIR) and scanning electron microscopy (SEM) and surface areas demonstrate the differences of physicochemical properties. Batch equilibrium experiments were conducted for various intervals extended to 96 h at 20, 25 and 30°C to investigate the efficiency of the sorbents in the removal of Cd(2+). CKD expressed high affinity for removal of Cd(2+) and was not affected by temperature, while AC was significantly affected, which reflects dissimilarity in the retention mechanisms defendant in CKD and those pursued by AC. The results were explained by changes of FTIR and SEM images before and after sorption experiments. The suggestion is that electrostatic ion exchange and complex reactions are the main mechanisms for Cd(2+) removal. The kinetic data were evaluated by fractional power, Elovich, pseudo-first order and pseudo-second-order kinetic models. The pseudo-second-order kinetic model was found to correlate with the experimental data well. These results revealed that CKD can be used as a cost-effective and efficient sorbent for Cd(2+) removal in comparison with AC. PMID:27054742

  17. Removal of boron from aqueous solution using magnetic carbon nanotube improved with tartaric acid

    PubMed Central

    2014-01-01

    Boron removal capacity of multi-walled carbon nanotubes (MWCNTs) modified with tartaric acid was investigated in this study. Modification of MWCNTs with tartaric acid was confirmed by Boehm surface chemistry method and fourier transform infra-red (FT-IR) spectroscopy. Experiments were performed to determine the adsorption isotherm and adsorption thermodynamic parameters of boron adsorption on tartaric acid modified MWCNTs (TA-MWCNTs). The effect of variables including initial pH, dosage of adsorbent, contact time and temperature was investigated. Analysis of data showed that adsorption equilibrium could be better described by Freundlich isotherm and the maximum adsorption capacities obtained at the pH of 6.0 was 1.97 mg/g. The estimated thermodynamic values of free energy (ΔG°), entropy (ΔS°) and enthalpy (ΔH°) indicated a spontaneous and an endothermic process. Furthermore, the TA-MWCNTs was magnetized for separation of boron-contaminated adsorbent from aqueous solution by applying magnetic field. The results showed that magnetic TA-MWCNTs particles were separated effectively after adsorption from contaminated water. PMID:24393401

  18. 2-chlorophenol sorption from aqueous solution using granular activated carbon and polymeric adsorbents

    NASA Astrophysics Data System (ADS)

    Ghatbandhe, A. S.; Jahagirdar, H. G.; Yenkie, M. K. N.; Deosarkar, S. D.

    2013-08-01

    Adsorption equilibrium and kinetics of 2-chlorophenol (2-CP) one of the chlorophenols (CPs) onto bituminous coal based Filtrasorb-400 grade granular activated carbon and three different types of polymeric adsorbents were studied in aqueous solution in a batch system. Langmuir isotherm models were applied to experimental equilibrium data of 2-CP adsorption. Equilibrium data fitted very well to the Langmuir equilibrium models of 2-CP. Adsorbent monolayer capacity Q Langmuir constant b and adsorption rate constants k a were evaluated. 2-CP adsorption using GAC is very rapid in the first hour of contact where 70-80% of the adsorbate is removed by GAC followed by a slow approach to equilibrium. Whereas in case of polymeric adsorbents 60-65% of the adsorbate is removed in the first 30 min which is then followed by a slow approach to equilibrium. The order of adsorption of 2-CP on different adsorbents used in the study is found to be in following order: F-400 > XAD-1180 > XAD-4 > XAD-7HP.

  19. Sorption of chlorophenols from aqueous solution by granular activated carbon, filter coal, pine and hardwood.

    PubMed

    Hossain, G S M; McLaughlan, R G

    2012-09-01

    Wood and coal, as low-cost sorbents, have been evaluated as an alternative to commercial granular activated carbon (GAC) for chlorophenol removal. Kinetic experiments indicated that filter coal had a significantly lower rate of uptake (approximately 10% of final uptake was achieved after three hours) than the other sorbents, owing to intra-particle diffusion limitations. The data fitted a pseudo-second-order model. Sorption capacity data showed that GAC had a high sorption capacity (294-467 mg g(-1)) compared with other sorbents (3.2-7.5 mg(g-1)). However, wood and coal had a greater sorption capacity per unit surface area than GAC. Sorption equilibrium data was best predicted using a Freundlich adsorption model. The sorption capacity for all sorbents was 2-chlorophenol < 4-chlorophenol < 2, 4-dichlorophenol, which correlates well with solute hydrophobicity, although the relative differences were much less for coal than the other sorbents. The results showed that pine, hardwood and filter coal can be used as sorbent materials for the removal of chlorophenol from water; however, kinetic considerations may limit the application of filter coal. PMID:23240177

  20. Degradation of carbon tetrachloride in aqueous solution in the thermally activated persulfate system.

    PubMed

    Xu, Minhui; Gu, Xiaogang; Lu, Shuguang; Qiu, Zhaofu; Sui, Qian; Miao, Zhouwei; Zang, Xueke; Wu, Xiaoliang

    2015-04-01

    Thermal activation of persulfate (PS) has been identified to be effective in the destruction of organic pollutants. The feasibility of carbon tetrachloride (CT) degradation in the thermally activated PS system was evaluated. The experimental results showed that CT could be readily degraded at 50 °C with a PS concentration of 0.5M, and CT degradation and PS consumption followed the pseudo-first order kinetic model. Superoxide radical anion (O2(*-)) was the predominant radical species responsible for CT degradation and the split of CCl was proposed as the possible reaction pathways for CT degradation. The process of CT degradation was accelerated by higher PS dose and lower initial CT concentration. No obvious effect of the initial pH on the degradation of CT was observed in the thermally activated PS system. Cl(*-), HCO3(*-), and humic acid (HA) had negative effects on CT degradation. In addition, the degradation of CT in the thermally activated PS system could be significantly promoted by the solvents addition to the solution. In conclusion, the thermally activated PS process is a promising option in in-situ chemical oxidation/reduction remediation for degrading highly oxidized organic contaminants such as CT that is widely detected in contaminated sites. PMID:25544995

  1. Mechanisms controlling the production and transport of methane, carbon dioxide, and dissolved solutes within a boreal peatland

    SciTech Connect

    Siegel, D.I.

    1992-04-09

    Peatlands are one of the most important terrestrial reservoirs in the global cycle for carbon, and are a major source for atmospheric methane. However, little is known about the dynamics of these carbon reservoirs or their feedback mechanisms with the pool of atmospheric CO{sub 2} during the Holocene. Specifically, it is unknown whether large peat basins are sources, sinks, or steady-state reservoirs for the global carbon cycle. In particular, the production and transport of methane, carbon dioxide, and dissolved organic carbon form the deeper portions of these peatlands is unknown. Our DOE research program is to conduct an integrated ecologic and hydrogeochemical study of the Glacial Lake Agassiz peatlands (northern Minnesota) to better understand the carbon dynamics in globally significant peat basins. Specifically, our study will provide local and regional data on (1), rates of carbon accumulation and loss and fluxes of methane in the peat profiles; (2) the physical and botanical factors controlling the production of methane and carbon dioxide in the wetland; and (3) the role of hydrogeologic processes in controlling the fluxes of gases and solutes through the peat. We intend to use computer simulation models, calibrated to field data, to scale-up from local to regional estimates of methane and carbon dioxide within the basin. How gases and dissolved organic carbon escapes form peatlands in unknown. It has been suggested that the concentrations of methane produced in the upper peat are sufficient to produce diffusion gradients towards the surface. Alternatively, gas may move through the peat profile by groundwater advection.

  2. Basic solutions to carbon/carbon oxidation: Science and technology. Final report, 15 April 1993--14 April 1998

    SciTech Connect

    Harrison, I.R.; Chung, T.; Pantano, C.; Radovic, L.; Thrower, P.

    1998-04-14

    The goal of this study was to gain a fundamental understanding of the role of boron in carbon oxidation. Boron-doped carbons were synthesized via CVD, ion implantation and high temperature doping are subsequently characterized. It was found that high temperature doped HOPG carbons were ideal for oxidation studies because their surface could be reproduced, their surface structures were determined and they were able to be characterized by XPS, AFM and SEM. The direct analysis of the chemical structures and atomic arrangements in boron- doped carbon or carbon surfaces by these techniques was critical in determining the effect of boron on carbon oxidation. XPS was utilized in this work to determine the local bonding environment of boron in carbon before an after oxidation. It was necessary to obtain an accurate calibration of the B1s binding energy scale which was accomplished by obtaining photoemission spectra of boron-doped carbons with known structures (local boron bonding environments), such as boron oxide, boron carbide, triphenylboroxine, tourmaline, boric acid, danburite and high temperature boron-doped graphite. All of the aforementioned standards contain boron in a unique bonding environment and thus their spectra formulated a complete conversion of B1s binding energies to boron chemical environments which has not been reported in the past. It was clearly established that a chemical shift for substitutional boron in graphite exists at 186.5 eV with a FWHM of 1.2. The chemical structures of the boron in the standards were related to the binding energy using a Pauling charge distribution model and a modification of the Sanderson electronegativity method. This approach was used to determine whether the B1s binding energy would change depending upon the specific location of boron in the graphite or graphite surface.

  3. Molecular-scale hydrophilicity induced by solute: molecular-thick charged pancakes of aqueous salt solution on hydrophobic carbon-based surfaces.

    PubMed

    Shi, Guosheng; Shen, Yue; Liu, Jian; Wang, Chunlei; Wang, Ying; Song, Bo; Hu, Jun; Fang, Haiping

    2014-01-01

    We directly observed molecular-thick aqueous salt-solution pancakes on a hydrophobic graphite surface under ambient conditions employing atomic force microscopy. This observation indicates the unexpected molecular-scale hydrophilicity of the salt solution on graphite surfaces, which is different from the macroscopic wetting property of a droplet standing on the graphite surface. Interestingly, the pancakes spontaneously displayed strong positively charged behavior. Theoretical studies showed that the formation of such positively charged pancakes is attributed to cation-π interactions between Na(+) ions in the aqueous solution and aromatic rings on the graphite surface, promoting the adsorption of water molecules together with cations onto the graphite surface; i.e., Na(+) ions as a medium adsorbed to the graphite surface through cation-π interactions on one side while at the same time bonding to water molecules through hydration interaction on the other side at a molecular scale. These findings suggest that actual interactions regarding carbon-based graphitic surfaces including those of graphene, carbon nanotubes, and biochar may be significantly different from existing theory and they provide new insight into the control of surface wettability, interactions and related physical, chemical and biological processes. PMID:25348642

  4. Molecular-scale Hydrophilicity Induced by Solute: Molecular-thick Charged Pancakes of Aqueous Salt Solution on Hydrophobic Carbon-based Surfaces

    PubMed Central

    Shi, Guosheng; Shen, Yue; Liu, Jian; Wang, Chunlei; Wang, Ying; Song, Bo; Hu, Jun; Fang, Haiping

    2014-01-01

    We directly observed molecular-thick aqueous salt-solution pancakes on a hydrophobic graphite surface under ambient conditions employing atomic force microscopy. This observation indicates the unexpected molecular-scale hydrophilicity of the salt solution on graphite surfaces, which is different from the macroscopic wetting property of a droplet standing on the graphite surface. Interestingly, the pancakes spontaneously displayed strong positively charged behavior. Theoretical studies showed that the formation of such positively charged pancakes is attributed to cation–π interactions between Na+ ions in the aqueous solution and aromatic rings on the graphite surface, promoting the adsorption of water molecules together with cations onto the graphite surface; i.e., Na+ ions as a medium adsorbed to the graphite surface through cation–π interactions on one side while at the same time bonding to water molecules through hydration interaction on the other side at a molecular scale. These findings suggest that actual interactions regarding carbon-based graphitic surfaces including those of graphene, carbon nanotubes, and biochar may be significantly different from existing theory and they provide new insight into the control of surface wettability, interactions and related physical, chemical and biological processes. PMID:25348642

  5. Multi-instrumental characterization of carbon nanotubes dispersed in aqueous solutions

    EPA Science Inventory

    Previous studies showed that the dispersion extent and physicochemical properties of carbon nanotubes are highly dependent upon the preparation methods (e.g., dispersion methods and dispersants). In the present work, multiwalled carbon nanotubes (MWNTs) are dispersed in aqueous s...

  6. Stress corrosion cracking of X-60 line pipe steel in a carbonate-bicarbonate solution

    SciTech Connect

    Pilkey, A.K.; Lambert, S.B.; Plumtree, A. . Dept. of Mechanical Engineering)

    1995-02-01

    An experimental system was developed to reproduce stress corrosion cracking (SCC) of API X-60 line pipe steels in highly alkaline (pH = 10) carbonate-bicarbonate (1 N sodium carbonate [Na[sub 2]CO[sub 3

  7. Preparation and structure analysis of carbon/carbon composite made from phenolic resin impregnation into exfoliated graphite

    NASA Astrophysics Data System (ADS)

    Chen, X.; Zheng, Y. P.; Kang, F.; Shen, W. C.

    2006-05-01

    Exfoliated graphite-based carbon/carbon composites were prepared using sequence processes of phenolic resin alcohol solution impregnation, carbonization and carbon dioxide (or steam) activation. The textural/structural characteristics of the composites were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), nitrogen adsorption and mercury porosimetry. The results indicated that the composites were composed of graphite and amorphous carbon. On the surface, the worm-like particles were covered by pyrolytic carbon, which also penetrated into parts of the interior pores of the particles. Macropores still remained in the composite, whereas micropores which were formed by the activation of pyrolytic carbon contributed to most of the pore volume.

  8. Carbon Solution in Core-Forming Magma Ocean Conditions: Implications for the Origin and Distribution of Terrestrial Carbon

    NASA Astrophysics Data System (ADS)

    Dasgupta, R.; Chi, H.; Walker, D.; Shimizu, N.; Buono, A. S.

    2012-12-01

    The origin of bulk silicate Earth carbon inventory is poorly known and the fate of the element during the early Earth differentiation and core formation is a missing link in the evolution of the terrestrial carbon cycle. Here we present high pressure-temperature experiments that simulate metal-silicate equilibria in a shallow magma ocean. Experiments were performed at 1-5 GPa, 1600-2100 °C on mixtures of synthetic or natural silicates (tholeiitic basalt/ alkali basalt/ komatiite/ fertile peridotite) and Fe-Ni-C±Co±S contained in graphite or MgO capsules. All the experiments produced immiscible Fe-rich metallic and silicate melts at oxygen fugacity (fO2) between ~IW-1.5 and IW-1.9. Carbon and hydrogen concentrations of basaltic glasses and non-glassy quenched silicate melts were determined using secondary ionization mass spectrometry (SIMS) and speciation of dissolved C-O-H volatiles in silicate glasses was constrained using Raman spectroscopy. Carbon contents of metallic melts were determined using both electron microprobe and SIMS. Our experiments indicate that at core-forming, reduced conditions, carbon in mafic-ultramafic magmas dissolves primarily as various hydrogenated species and the total carbon storage capacity, although is significantly higher than solubility of CO2 under similar conditions, remains low (<500 ppm). The total carbon content in our reduced melts at graphite saturation increases with increasing melt depolymerization (NBO/T), consistent with recent spectroscopic studies [1], and modestly with increasing hydration. Carbon behaves as a metal loving element during core-mantle separation and metal/silicate carbon partition coefficient, DC varies between ~3500 and ≥150 and increases with increasing pressure and decreases with increasing temperature and melt NBO/T. Extrapolation of our data to the plausible conditions of core-mantle equilibration suggest that if only a trace amount of carbon (~730 ppm C; [2]) was available during early Earth

  9. Activity and stability of immobilized carbonic anhydrase for promoting CO2 absorption into a carbonate solution for post-combustion CO2 capture

    USGS Publications Warehouse

    Zhang, S.; Zhang, Z.; Lu, Y.; Rostam-Abadi, M.; Jones, A.

    2011-01-01

    An Integrated Vacuum Carbonate Absorption Process (IVCAP) currently under development could significantly reduce the energy consumed when capturing CO2 from the flue gases of coal-fired power plants. The biocatalyst carbonic anhydrase (CA) has been found to effectively promote the absorption of CO2 into the potassium carbonate solution that would be used in the IVCAP. Two CA enzymes were immobilized onto three selected support materials having different pore structures. The thermal stability of the immobilized CA enzymes was significantly greater than their free counterparts. For example, the immobilized enzymes retained at least 60% of their initial activities after 90days at 50??C compared to about 30% for their free counterparts under the same conditions. The immobilized CA also had significantly improved resistance to concentrations of sulfate (0.4M), nitrate (0.05M) and chloride (0.3M) typically found in flue gas scrubbing liquids than their free counterparts. ?? 2011 Elsevier Ltd.

  10. Toward a zero-carbon energy policy in Europe: defining a viable solution

    SciTech Connect

    Jones, Christopher; Glachant, Jean-Michel

    2010-04-15

    The present pace of carbon emission is not sustainable. Human societies need to react and to change. A rational responsive policy to deliver the required carbon emission reduction can be delineated if the key objective parameters are identified and addressed. This article attempts to lay the groundwork for a viable carbon energy policy for Europe. (author)

  11. The radiation induced chemistry of uranyl cation in aqueous carbonate –bicarbonate solutions as followed by NMR spectroscopy

    SciTech Connect

    McNamara, Bruce K.; Snow, Lanee A.; Soderquist, Chuck Z.; Sinkov, Sergei I.; Cho, Herman M.; Friese, Judah I.

    2006-05-01

    Alpha radiation induced formation of hydrogen peroxide in carbonate ?bicarbonate media was followed by 13C NMR using dissolved [233UO2(13CO3)3]4- as the alpha source (Dalpha= 12.1 Gy/hr). Between the pH region between 5.9 and 11.6 hydrogen peroxide causes a varied speciation of the uranyl carbonates that is a function of the uranium, carbonate and the hydrogen peroxide concentrations. It is shown that the speciation of the peroxy carbonates (or other species) formed in solution by titration with hydrogen peroxide are common to those formed by hydrogen peroxide generated by radiolysis. The radiolysis experiment was carried out above pH = 9.96 to minimize the loss of 13CO2 over a 2800 hr period. Radiolytic generation of hydrogen peroxide was followed by formation of a uranyl peroxy carbonate complex and complex formation accelerated for about 1200 hours. Complex formation was observed to terminate at a concentration between 1x10-4 and 5x10-4 M. It is assumed that either a steady state H2O2 production rate was established in solution or that some limiting feature of the experiment was responsible for slowing the yield of product.

  12. Alkali promoted molybdenum (IV) sulfide based catalysts, development and characterization for alcohol synthesis from carbon monoxide and hydrogen

    NASA Astrophysics Data System (ADS)

    Molina, Belinda Delilah

    For more than a century transition metal sulfides (TMS) have been the anchor of hydro-processing fuels and upgrading bitumen and coal in refineries worldwide. As oil supplies dwindle and environmental laws become more stringent, there is a greater need for cleaner alternative fuels and/or synthetic fuels. The depletion of oil reserves and a rapidly increasing energy demand worldwide, together with the interest to reduce dependence on foreign oil makes alcohol production for fuels and chemicals via the Fischer Tropsch synthesis (FTS) very attractive. The original Fischer-Tropsch (FT) reaction is the heart of all gas-to-liquid technologies; it creates higher alcohols and hydrocarbons from CO/H2 using a metal catalyst. This research focuses on the development of alkali promoted MoS2-based catalysts to investigate an optimal synthesis for their assistance in the production of long chain alcohols (via FTS) for their use as synthetic transportation liquid fuels. Properties of catalytic material are strongly affected by every step of the preparation together with the quality of the raw materials. The choice of a laboratory method for preparing a given catalyst depends on the physical and chemical characteristics desired in the final composition. Characterization methods of K0.3/Cs0.3-MoS2 and K0.3 /Cs0.3-Co0.5MoS2 catalysts have been carried out through Scanning Electron Microscopy (SEM), BET porosity and surface analysis, Transmission Electron Microscopy (TEM) and X-Ray Diffraction (XRD). Various characterization methods have been deployed to correlate FTS products versus crystal and morphological properties of these heterogeneous catalysts. A lab scale gas to liquid system has been developed to evaluate its efficiency in testing FT catalysts for their production of alcohols.

  13. Detection and determination of solute carbon in grain interior to correlate with the overall carbon content and grain size in ultra-low-carbon steel.

    PubMed

    Dong, Jiling; He, Yinsheng; Lee, Chan-Gyu; Lee, Byungho; Yoon, Jeongbong; Shin, Keesam

    2013-08-01

    In this study, every effort was exerted to determine and accumulate data to correlate microstructural and compositional elements in ultra-low-carbon (ULC) steels to variation of carbon content (12-44 ppm), manganese (0.18-0.36%), and sulfur (0.0066-0.001%). Quantitative analysis of the ULC steel using optical microscope, scanning electron microscope, transmission electron microscope, and three-dimensional atom probe revealed the decrease of grain size and dislocation density with the increase of carbon contents and/or increase of the final delivery temperature. For a given carbon content, the grain interior carbon concentration increases as the grain size increases. PMID:23920177

  14. Alcoholism and Alcohol Abuse

    MedlinePlus

    ... increase the risk of certain cancers. It can cause damage to the liver, brain, and other organs. Drinking during pregnancy can harm your baby. Alcohol also increases the risk of death from car crashes, injuries, homicide, and suicide. If you want to stop drinking, there is ...

  15. A SEARCH FOR INTERSTELLAR CARBON-CHAIN ALCOHOL HC{sub 4}OH IN STAR-FORMING REGION L1527 AND DARK CLOUD TMC-1

    SciTech Connect

    Araki, Mitsunori; Yamabe, Hiromichi; Koshikawa, Naohiro; Tsukiyama, Koichi; Takano, Shuro; Nakane, Aya; Okabayashi, Toshiaki; Kunimatsu, Arisa; Kuze, Nobuhiko

    2012-01-10

    We report a sensitive search for the rotational transitions of the carbon-chain alcohol HC{sub 4}OH in the frequency range 21.2-46.7 GHz in the star-forming region L1527 and the dark cloud TMC-1. The motivation was laboratory detection of HC{sub 4}OH by microwave spectroscopy. Despite achieving rms noise levels of several millikelvin in the antenna temperature using the 45 m telescope at Nobeyama Radio Observatory, the detection was not successful, leading to 3{sigma} upper limits corresponding to the column densities of 2.0 Multiplication-Sign 10{sup 12} and 5.6 Multiplication-Sign 10{sup 12} cm{sup -2} in L1527 and TMC-1, respectively. These upper limits indicate that [HC{sub 4}OH]/[HC{sub 5}N] ratios are less than 0.3 and 0.1 in L1527 and TMC-1, respectively, where HC{sub 5}N is an HC{sub 4}-chain cyanide and HC{sub 4}OH is a hydroxide. These ratios suggest that the cyano carbon-chain molecule dominates the hydroxyl carbon-chain molecule in L1527 and TMC-1. This is contrary to the case of saturated compounds in hot cores, e.g., CH{sub 3}OH and CH{sub 3}CN, and can be a chemical feature of carbon-chain molecules in L1527 and TMC-1. In addition, the column densities of the 'unsubstituted' carbon-chain molecule C{sub 4}H and the sulfur-bearing molecules SO and HCS{sup +} were determined from detected lines in L1527.

  16. Surface modification of activated carbon for enhanced adsorption of perfluoroalkyl acids from aqueous solutions.

    PubMed

    Zhi, Yue; Liu, Jinxia

    2016-02-01

    The objective of the research was to examine the effect of increasing carbon surface basicity on uptake of perfluorooctane sulfonic (PFOS) and carboxylic acids (PFOA) by activated carbon. Granular activated carbons made from coal, coconut shell, wood, and phenolic-polymer-based activated carbon fibers were modified through high-temperature and ammonia gas treatments to facilitate systematical evaluation of the impact of basicity of different origins. Comparison of adsorption isotherms and adsorption distribution coefficients showed that the ammonia gas treatment was more effective than the high-temperature treatment in enhancing surface basicity. The resultant higher point of zero charges and total basicity (measured by total HCl uptake) correlated with improved adsorption affinity for PFOS and PFOA. The effectiveness of surface modification to enhance adsorption varied with carbon raw material. Wood-based carbons and activated carbon fibers showed enhancement by one to three orders of magnitudes while other materials could experience reduction in adsorption towards either PFOS or PFOA. PMID:26469934

  17. Adsorption of chlorophenols from aqueous solutions by pristine and surface functionalized single-walled carbon nanotubes.

    PubMed

    Ding, Han; Li, Xin; Wang, Jun; Zhang, Xiaojian; Chen, Chao

    2016-05-01

    The adsorption of six kinds of chlorophenols on pristine, hydroxylated and carboxylated single-walled carbon nanotubes (SWCNTs) has been investigated. Pseudo-first order and pseudo-second order models were used to describe the kinetic data. All adsorption isotherms were well fitted with Langmuir, Freundlich and Polanyi-Manes models, due to surface adsorption dominating the adsorption process. The close linear relationship between logKow and logKd suggested that hydrophobicity played an important role in the adsorption. The SWCNTs' adsorption capacity for chlorophenols was weakened by addition of oxygen-containing functional groups on the surface, due to the loss of specific surface area, the increase of hydrophilicity and the reduction of π-π interaction. The best adsorption capacity of pristine SWCNTs, SWCNT-OH and SWCNT-COOH for six chlorophenols varied from 19 to 84mg/g, from 19 to 65mg/g and from 17 to 65mg/g, respectively. The effect of pH on the adsorption of 2,6-dichlorophenol (2,6-DCP), was also studied. When pH is over the pKa of 2,6-dichlorophenol (2,6-DCP), its removal dropped sharply. When ionic strength increased (NaCl or KCl concentration from 0 to 0.02mmol/L), the adsorption capacity of 2,6-DCP on pristine SWCNTs decreased slightly. The comparison of chlorophenols adsorption by SWCNTs, MWCNTs and PAC was made, indicating that the adsorption rate of CNTs was much faster than that of PAC. The results provide useful information about the feasibility of SWCNTs as an adsorbent to remove chlorophenols from aqueous solutions. PMID:27155424

  18. The effect of purification of single-walled carbon nanotube bundles on the alcohol sensitivity of nanocomposite Langmuir Blodgett films for SAW sensing applications

    NASA Astrophysics Data System (ADS)

    Penza, M.; Tagliente, M. A.; Aversa, P.; Re, M.; Cassano, G.

    2007-05-01

    HiPco (high-pressure CO dissociation process) single-walled carbon nanotube (SWCNT) bundles containing Fe particles were purified in a two-step purification process by thermal annealing in oxygen and post-treatment in HCl. Nanocomposite films of pristine and purified SWCNTs embedded in an organic matrix of cadmium arachidate (CdA) were prepared by a Langmuir-Blodgett (LB) molecular engineering technique with a fixed weight filler content of 75 wt% onto a surface acoustic wave (SAW) transducer operating as an oscillator at a frequency of 433 MHz. The raw and purified samples were characterized at various stages of the purification process using thermogravimetric analysis (TGA), high-resolution transmission electron microscopy (HR-TEM), along with energy-dispersive x-ray spectroscopy (EDS), field emission scanning electron microscopy (FE-SEM) and x-ray diffraction (XRD). Functional characterizations of the SWCNT-nanocomposite-based SAW sensors were investigated towards methanol, isopropanol and ethanol, and demonstrated high sensitivity, reversibility, fast response and ppm level detection at room temperature. Results indicate that the sensitivity of the SAW sensors based on a nanocomposite film of oxygen-annealed SWCNTs is enhanced to the alcohols tested at room temperature. Purification of the SWCNTs in the nanocomposite film affects the SAW sensitivity to alcohol by modulating the sensing properties. The sensing mechanisms are analysed and discussed.

  19. Weak intramolecular and intermolecular hydrogen bonding of benzyl alcohol, 2-phenylethanol and 2-phenylethylamine in the adsorption on graphitized thermal carbon black.

    PubMed

    Varfolomeeva, V V; Terentev, A V

    2015-10-01

    The paper discusses the role of weak intra- and intermolecular hydrogen bonds in the adsorption of benzyl alcohol, 2-phenylethanol and 2-phenylethylamine on graphitized thermal carbon black (GTCB). Using the B3LYP/aug-cc-pVDZ, B3LYP/aug-cc-pVTZ methods and the molecular-statistical theory of adsorption we found the structural and energetic parameters of the conformers to be stable in the gas phase and in the adsorbed state. The contribution of weak OHπ, NHπ, CHO hydrogen bonds to the stabilization of the conformers was defined by the method of non-covalent interactions (NCI). Based on the difference in the experimental and calculated values of the Henry constant Δ ln K1 < 0.25 (K1, cm(3) m(-2)) a high predictive power of molecular-statistical calculation of the thermodynamic characteristics of adsorption (TCA) has been shown. To obtain a high predictive power of molecular-statistical calculation it was necessary to take due account of the structural features of flexible molecules in the adsorbed state. A significant impact of the weak OHπGTCB intermolecular hydrogen bond of benzyl alcohol on the TCA values has been established. PMID:26327209

  20. Synthesis and utilization of a novel carbon nanotubes supported nanocables for the adsorption of dyes from aqueous solutions

    NASA Astrophysics Data System (ADS)

    Liu, Wei; Jiang, Xinyu; Chen, Xiaoqing

    2015-09-01

    Using multiwalled carbon nanotubes(MWCNTs) as mechanical support and glucose as carbon resource, a hydrothermal carbonization route was designed for the synthesis of MWCNTs@carbon nanocables with tunable diameter and length. MWCNTs are firstly used as templates for the formation of carbon-rich composite nanocables, and the diameter of the nanocables could be tailored through adjusting the hydrothermal time or the ratio of MWCNTs and glucose. Owing to abundant superficial oxygen-containing functional groups, porous surface and remarkable reactivity, the as-synthesized nanocables are capable of efficiently adsorbing cationic dye methylene blue (MB) and crystal violet (CV). Furthermore, the optimum adsorption conditions, kinetics, adsorption isotherms and adsorption thermodynamics of dyes were studied systematically. Additionally, the maximum adsorption capacities calculated from data analysis (298.5 mg/g for MB and 228.3 mg/g for CV) are significant higher than those of raw MWCNTs and some other adsorbents reported previously, which provides strong evidence for using MWCNTs@carbon nanocables as adsorbent to remove dyes from aqueous solutions.

  1. IGA of alloy 600 in high-temperature solutions of sodium hydroxide contaminated with carbonate. Final report. [PWR

    SciTech Connect

    Roberge, R.; Bandy, R.; van Rooyen, D.

    1983-05-01

    Alloy 600 was tested in sodium hydroxide contaminated with sodium carbonate at 300/sup 0/C and 315/sup 0/C to examine its resistance to intergranular attack (IGA) under controlled cathodic and anodic potentials. Specimens of alloy 600 were studied as C-rings under constant deflection, wires under constant load and wires without any applied tensile stress. The material was mainly used in its mill annealed condition, although some specimens were studied as solution annealed and solution annealed plus sensitized. Unlike the last two metallurgical states, the mill annealed alloy 600 material was rather sensitive to stress corrosion cracking (SCC) in a range of anodic potentials.

  2. Nanosized CuO and ZnO Catalyst Supported on Honeycomb-Typed Monolith for Hydrogenation of Carbon Dioxide to Methyl Alcohol.

    PubMed

    Park, Chul-Min; Ahn, Won-Ju; Jo, Woong-Kyu; Song, Jin-Hun; Oh, Chang-Yeop; Jeong, Young-Shin; Chung, Min-Chul; Park, Kwon-Pil; Kim, Ki-Joong; Jeong, Woon-Jo; Sohn, Bo-Kyun; Jung, Sang-Chul; Lee, Do-Jin; Ahn, Byeong-Kwon; Ahn, Ho-Geun

    2015-01-01

    The greenhouse effect of carbon dioxide (CO2) has been recognized as one of the most serious problems in the world. Conversion of CO2 to methyl alcohol (CH3OH) was studied using catalytic chemical methods. Honeycomb-typed monolith used as catalyst support was 400 cell/inch2. Pretreatment of the monolith surface was carried out by thermal treatment and acid treatment. Monolith-supported nanosized CuO-ZnO catalysts were prepared by wash-coat method. The prepared catalysts were characterized by using SEM, TEM, and XRD. The catalytic activity for CO2 hydrogenation to CH3OH was investigated using a flow-type reactor with varying reaction temperature, reaction pressure and contact time. Conversion of CO2 was increased with increasing reaction temperature, but selectivity to CH3OH was decreased. Optimum reaction temperature was about 250 degrees C under 20 atm. Because of the reverse water gas shift reaction. PMID:26328404

  3. Study of caffeine as corrosion inhibitors of carbon steel in chloride solution containing hydrogen sulfide using electrochemical impedance spectroscopy (EIS)

    NASA Astrophysics Data System (ADS)

    Solehudin, Agus; Berman, Ega Taqwali; Nurdin, Isdiriayani

    2015-09-01

    The corrosion behaviour of steel surface in the absence and presence of caffeine in 3.5% NaCl solution containing dissolved H2S gas is studied using electrochemical impedance spectroscopy (EIS). The experimental results of carbon steel corrosion in 3.5% NaCl solution containing 500 mg/l H2S at different caffeine concentrations showed that corrosion rate of carbon steel decreases with increasing of caffeine concentrations from 0 to 0,1 mmol/l. Whereas, the corrosion rate increase with increasing of caffeine concentrations from 1 to 10 mmol/l. It is clear that no inhibition efficiency increases with increasing inhibitor concentration. The optimum value of inhibition efficiency was 90% at a caffeine concentration of 0.1 mmol/l. This suggests that caffeine's performance as a corrosion inhibitor is more effective at a concentration of 0.1 mmol/l.

  4. Adsorption of Nickel (II) from Aqueous Solution by Bicarbonate Modified Coconut Oilcake Residue Carbon.

    PubMed

    Vijayakumari, N; Srinivasan, K

    2014-07-01

    The adsorption of Ni (II) on modified coconut oilcake residue carbon (bicarbonate treated coconut oilcake residue carbon-BCORC) was employed for the removal of Ni (II) from water and wastewater. The influence of various factors such as agitation time, pH and carbon dosage on the adsorption capacity has been studied. Adsorption isothermal data could be interpreted by Langmuir and Freundlich equations. In order to understand the reaction mechanism, kinetic data has been studied using reversible first order rate equation. Similar studies were carried out using commercially available activated carbon--CAC, for comparison purposes. Column studies were conducted to obtain breakthrough capacities of BCORC and CAC. Common anions and cations affecting the removal of Ni (II) on both the carbons were also studied. Experiments were also done with wastewater containing Ni (II), to assess the potential of these carbons. PMID:26563074

  5. A Study of the Solvation Structure of L-Leucine in Alcohol-Water Binary Solvents through Molecular Dynamics Simulations and FTIR and NMR Spectroscopy.

    PubMed

    Takamuku, Toshiyuki; Hatomoto, Yohei; Tonegawa, Junko; Tsutsumi, Youichi; Umecky, Tatsuya

    2015-10-26

    The solvation structures of l-leucine (Leu) in aliphatic-alcohol-water and fluorinated-alcohol-water solvents are elucidated for various alcohol contents by using molecular dynamics (MD) simulations and IR, and (1) H and (13) C NMR spectroscopy. The aliphatic alcohols included methanol, ethanol, and 2-propanol, whereas the fluorinated alcohols were 2,2,2-trifluoroethanol and 1,1,1,3,3,3-hexafluoro-2-propanol. The MD results show that the hydrophobic alkyl moiety of Leu is surrounded by the alkyl or fluoroalkyl groups of the alcohol molecules. In particular, TFE and HFIP significantly solvate the alkyl group of Leu. IR spectra reveal that the Leu C-H stretching vibration blueshifts in fluorinated alcohol solutions with increasing alcohol content, whereas the vibration redshifts in aliphatic alcohol solutions. When the C-H stretching vibration blueshifts in the fluorinated alcohol solutions, the hydrogen and carbon atoms of the Leu alkyl group are magnetically shielded. Consequently, TFE and HFIP molecules may solvate the Leu alkyl group through the blue-shifting hydrogen bonds. PMID:26289908

  6. Degradation of alkanolamines in gas-treating solutions: Kinetics of Di-2-propanolamine degradation in aqueous solutions containing carbon dioxide

    SciTech Connect

    Kim, C.J.

    1988-01-01

    The rates and products of degradation of di-2-propanolamine (DIPA) were measured at 100-120/sup 0/C in the presence of a controlled amount of CO/sub 2/. DIPA underwent facile degradation, giving 3-(2-hydroxypropyl)-5-methyl-2-oxazolidone (HPMO) as the main product. Hydrolysis of HPMO occurs readily, but its equilibrium concentration increases with increasing amounts of CO/sub 2/ in solution. A kinetic model was derived and compared with the previously established model for diethanolamines (DEA) degradation. The virtual absence of di- or triamino degradation products is the most striking feature of DIPA degradation, which may be contrasted with the facile formation of di- and triamino products from DEA. This difference is discussed in terms of steric inhibition of the reaction, HPMO + DIPA ..-->.. diamino compounds.

  7. Coagulation of chitin and cellulose from 1-ethyl-3-methylimidazolium acetate ionic-liquid solutions using carbon dioxide.

    PubMed

    Barber, Patrick S; Griggs, Chris S; Gurau, Gabriela; Liu, Zhen; Li, Shan; Li, Zengxi; Lu, Xingmei; Zhang, Suojiang; Rogers, Robin D

    2013-11-18

    Chemisorption of carbon dioxide by 1-ethyl-3-methylimidazolium acetate ([C2 mim][OAc]) provides a route to coagulate chitin and cellulose from [C2 mim][OAc] solutions without the use of high-boiling antisolvents (e.g., water or ethanol). The use of CO2 chemisorption as an alternative coagulating process has the potential to provide an economical and energy-efficient method for recycling the ionic liquid. PMID:24115399

  8. Electrochemical studies of the film formation on lithium in propylene carbonate solutions under open-circuit conditions

    SciTech Connect

    Geronov, Y.; Schwager, F.; Muller, R.H.

    1981-11-01

    The nature of protective surface layers formed on lithium in propylene carbonate solutions of LiClO/sub 4/ and LiAsF/sub 6/ at open circuit has been investigated by electrochemical pulse measurements. The results are consistent with the fast formation of a compact thin layer resulting from the reaction with residual water. This layer acts as a solid ionic conductor. Slow corrosion or decomposition processes produce a thicker porous overlayer.

  9. The impact of carbon and oxygen in alpha-titanium: ab initio study of solution enthalpies and grain boundary segregation

    NASA Astrophysics Data System (ADS)

    Aksyonov, D. A.; Hickel, T.; Neugebauer, J.; Lipnitskii, A. G.

    2016-09-01

    The solution, grain boundary (GB) segregation, and co-segregation of carbon and oxygen atoms in α-titanium are studied using density functional theory. For five titanium tilt boundaries, including T1, T2, and C1 twin systems, we determine the GB structure, as well as GB energy and excess volume. The segregation energies and volumes of carbon and oxygen are calculated for 23 inequivalent interstitial voids, while for co-segregation 75 configurations are considered. It is obtained that depending on the type of the segregation void both a positive and a negative segregation process is possible. The physical reasons of segregation are explained in terms of the analysis of the void atomic geometry, excess volume and features of the electronic structure at the Fermi level. Although carbon and oxygen show qualitatively similar properties in α-Ti, several distinctions are observed for their segregation behavior and mutual interactions.

  10. The impact of carbon and oxygen in alpha-titanium: ab initio study of solution enthalpies and grain boundary segregation.

    PubMed

    Aksyonov, D A; Hickel, T; Neugebauer, J; Lipnitskii, A G

    2016-09-28

    The solution, grain boundary (GB) segregation, and co-segregation of carbon and oxygen atoms in α-titanium are studied using density functional theory. For five titanium tilt boundaries, including T1, T2, and C1 twin systems, we determine the GB structure, as well as GB energy and excess volume. The segregation energies and volumes of carbon and oxygen are calculated for 23 inequivalent interstitial voids, while for co-segregation 75 configurations are considered. It is obtained that depending on the type of the segregation void both a positive and a negative segregation process is possible. The physical reasons of segregation are explained in terms of the analysis of the void atomic geometry, excess volume and features of the electronic structure at the Fermi level. Although carbon and oxygen show qualitatively similar properties in α-Ti, several distinctions are observed for their segregation behavior and mutual interactions. PMID:27460043

  11. Synthesis and utilization of a novel carbon nanotubes supported nanocables for the adsorption of dyes from aqueous solutions

    SciTech Connect

    Liu, Wei; Jiang, Xinyu; Chen, Xiaoqing

    2015-09-15

    Using multiwalled carbon nanotubes(MWCNTs) as mechanical support and glucose as carbon resource, a hydrothermal carbonization route was designed for the synthesis of MWCNTs@carbon nanocables with tunable diameter and length. MWCNTs are firstly used as templates for the formation of carbon-rich composite nanocables, and the diameter of the nanocables could be tailored through adjusting the hydrothermal time or the ratio of MWCNTs and glucose. Owing to abundant superficial oxygen-containing functional groups, porous surface and remarkable reactivity, the as-synthesized nanocables are capable of efficiently adsorbing cationic dye methylene blue (MB) and crystal violet (CV). Furthermore, the optimum adsorption conditions, kinetics, adsorption isotherms and adsorption thermodynamics of dyes were studied systematically. Additionally, the maximum adsorption capacities calculated from data analysis (298.5 mg/g for MB and 228.3 mg/g for CV) are significant higher than those of raw MWCNTs and some other adsorbents reported previously, which provides strong evidence for using MWCNTs@carbon nanocables as adsorbent to remove dyes from aqueous solutions. - Graphical abstract: MWCNTs@carbon nanocables has been successfully fabricated by a hydrothermal carbonization method. The as-synthesized novel samples were used as adsorbents and exhibited high adsorption capacity on MB and CV. - Highlights: • A simple, cost-effective and “green” method for the synthesis of the material. • The diameter and length of the material are relatively easy to control. • The surface has large oxygen-containing groups and preferable chemical reactivity. • Compared with raw MWCNTs and some other adsorbents, the adsorption capacity is much high.

  12. Alcohol Calorie Calculator

    MedlinePlus

    ... Alcohol Calorie Calculator Weekly Total 0 Calories Alcohol Calorie Calculator Find out the number of beer and ... Calories College Alcohol Policies Interactive Body Calculators Alcohol Calorie Calculator Alcohol Cost Calculator Alcohol BAC Calculator Alcohol ...

  13. Utilization of activated carbon produced from fruit juice industry solid waste for the adsorption of Yellow 18 from aqueous solutions.

    PubMed

    Angin, Dilek

    2014-09-01

    The use of activated carbon obtained from sour cherry (Prunus cerasus L.) stones for the removal of a basic textile dye, which is Yellow 18, from aqueous solutions at different contact times, pH values and solution temperatures was investigated. The surface area and micropore volume of chemically modified activated carbon were 1704 m(2) g(-1) and 0.984 cm(3) g(-1), respectively. The experimental data indicated that the adsorption isotherms were well described by the Langmuir equilibrium isotherm equation and the calculated adsorption capacity was 75.76 mg g(-1) at 318 K. The adsorption kinetic of Yellow 18 obeys the pseudo-second-order kinetic model. The thermodynamic parameters were calculated to estimate the nature of adsorption. The activation energy of the system was calculated as 0.71-2.36 kJ/mol. According to these results, prepared activated carbon could be used as a low-cost adsorbent to compare with the commercial activated carbon for the removal of Yellow 18 from wastewater. PMID:24656549

  14. Understanding the Impact of Poly(ethylene oxide) on the Assembly of Lignin in Solution toward Improved Carbon Fiber Production.

    PubMed

    Imel, Adam E; Naskar, Amit K; Dadmun, Mark D

    2016-02-10

    Carbon fiber produced from lignin has recently become an industrial scalable product with applications ranging from thermal insulation to reinforcing automobile bodies. Previous research has shown that mixing 1-2 wt %, of poly(ethylene oxide) (PEO) with the lignin before fiber formation can enhance the properties of the final carbon fibers. The research reported here determines the impact of adding PEO to a lignin solution on its assembly, focusing on the role of the lignin structure on this assembly process. Results indicate the addition of PEO anisotropically directs the self-assembly of the hardwood and softwood lignin by lengthening the cylindrical building blocks that make up the larger global aggregates. On the other hand, results from an annual lignin exhibit a shapeless, more complex structure with a unique dependence on the PEO loading. These results are consistent with improved carbon fibers from solutions of lignin that include PEO, as the local ordering and directed assembly will inhibit the formation of defects during the carbon fiber fabrication process. PMID:26756927

  15. The adsorption and inhibition effect of calcium lignosulfonate on Q235 carbon steel in simulated concrete pore solution

    NASA Astrophysics Data System (ADS)

    Wang, Yishan; Zuo, Yu; Zhao, Xuhui; Zha, Shanshan

    2016-08-01

    The corrosion inhibition of calcium lignosulfonate (CLS) for Q235 carbon steel in saturated Ca(OH)2 + 0.1 mol/L NaCl solution was studied by means of weight loss, polarization, fluorescence microscopy (FM), scanning electron microscopy/energy dispersive spectrometry (SEM/EDS), microscopic infrared spectral imaging (M-IR) and X-ray photoelectron spectroscopy (XPS). For the steel in simulated concrete pore solution (pH 12.6), an increase of Eb value and a decrease of icorr value occurred with different concentrations of CLS. The optimal content of CLS was 0.001 mol/L at which the inhibition rate was 98.86% and the Eb value increased to 719 mV after 10 h of immersion. In mortar solution and in reinforced concrete environment, CLS also showed good inhibition for steel. The preferential adsorption of CLS around pits was detected by M-IR. The result illustrates that at the early stage the adsorption of CLS was heterogeneous and CLS may have a competitive adsorption with chloride ions at the active sites, which would be beneficial for decreasing the susceptibility of pitting corrosion. After the pre-filming time, an intact adsorption CLS film formed on carbon steel surface. The adsorption between CLS and calcium presented as Casbnd Osbnd S bonds. The adsorption of CLS on carbon steel surface occurred probably by both physisorption and chemisorption.

  16. Low carbon flower buildup, low smoke, and efficient diesel operation with vegetable oils by conversion to mono-esters and blending with diesel oil or alcohols

    SciTech Connect

    Nobukazu, T.; Itow, K.

    1984-01-01

    The purpose of this investigation is to evaluate the feasibility of rapeseed oil and palm oil for diesel fuel substitution in a naturally aspirated DI Diesel engine is evaluated. Means to reduce the carbon deposit buildup in vegetable oil combustion is found. In the experiments, the engine performance, exhaust gas emissions, and carbon deposits are measured for a number of fuels: rapeseed oil, palm oil, methylester of rapeseed oil, and these fuels blended with ethanol or diesel fuel with different fuel temperatures. Both of the vegetable oil fuels generate an acceptable engine performance and exhaust gas emission levels for short term operation, but they cause carbon deposit buildups and sticking of piston rings after extended operation. Practical solutions to overcome the problems are: increasing the fuel temperature to over 200/sup 0/C, blending 25 vol % diesel fuel in the vegetable oil, blending 20 vol % ethanol in the fuel, or converting the vegetable oils into methylesters.

  17. Mechanical and electromagnetic interference shielding Properties of poly(vinyl alcohol)/graphene and poly(vinyl alcohol)/multi-walled carbon nanotube composite nanofiber mats and the effect of Cu top-layer coating.

    PubMed

    Fujimori, Kazushige; Gopiraman, Mayakrishnan; Kim, Han-Ki; Kim, Byoung-Suhk; Kim, Ick-Soo

    2013-03-01

    We report the mechanical property and electromagnetic interference shielding effectiveness (EMI SE) of poly(vinyl alcohol) (PVA)/graphene and PVA/multi-walled carbon nanotube (MWCNT) composite nanofibers prepared by electrospinning. The metal (Cu) was deposited on the resultant PVA composite nanofibers using metal deposition technique in order to improve the mechanical properties and EMI shielding properties. The resulting PVA composite nanofibers and Cu-deposited corresponding nanofibers were characterized by field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and wide angle X-ray diffraction (WAXD). Tensile tests were performed on the PVA/graphene and PVA/MWCNT composite nanofibers. The tensile strength of the PVA/graphene and PVA/MWCNT composite nanofibers was found to be 19.2 +/- 0.3 MPa at graphene content - 6.0 wt% and 12.2 +/- 0.2 MPa at MWCNT content - 3.0 wt%, respectively. The EMI SE of the Cu-deposited PVA/graphene composite nanofibers was significantly improved compared to pure PVA/graphene composite nanofibers, and also depended on the thickness of Cu metal layer deposited on the PVA composite nanofibers. PMID:23755586

  18. Carbon Dioxide Effects on Ethanol Production, Pyruvate Decarboxylase, and Alcohol Dehydrogenase Activities in Anaerobic Sweet Potato Roots 1

    PubMed Central

    Chang, Ling A.; Hammett, Larry K.; Pharr, David M.

    1983-01-01

    The effect of varied anaerobic atmospheres on the metabolism of sweet potato (Ipomoea batatas [L.] Lam.) roots was studied. The internal gas atmospheres of storage roots changed rapidly when the roots were submerged under water. O2 and N2 gases disappeared quickly and were replaced by CO2. There were no appreciable differences in gas composition among the four cultivars that were studied. Under different anaerobic conditions, ethanol concentration in the roots was highest in a CO2 environment, followed by submergence and a N2 environment in all the cultivars except one. A positive relationship was found between ethanol production and pyruvate decarboxylase activity from both 100% CO2-treated and 100% N2-treated roots. CO2 atmospheres also resulted in higher pyruvate decarboxylase activity than did N2 atmospheres. Concentrations of CO2 were higher within anaerobic roots than those in the ambient anaerobic atmosphere. The level of pyruvate decarboxylase and ethanol in anaerobic roots was proportional to the ambient CO2 concentration. The measurable activity of pyruvate decarboxylase that was present in the roots was about 100 times less than that of alcohol dehydrogenase. Considering these observations, it is suggested that the rate-limiting enzyme for ethanol biosynthesis in sweet potato storage roots under anoxia is likely to be pyruvate decarboxylase rather than alcohol dehydrogenase. PMID:16662798

  19. Multi-walled carbon nanotubes and poly(lactic acid) nanocomposite fibrous membranes prepared by solution blow spinning.

    PubMed

    Oliveira, Juliano E; Zucolotto, Valtencir; Mattoso, Luiz H C; Medeiros, Eliton S

    2012-03-01

    Nanocomposite fibers based on multi-walled carbon nanotubes (MWCNT) and poly(lactic acid) (PLA) were prepared by solution blow spinning (SBS). Fiber morphology was characterized by scanning electron microscopy (SEM) and optical microscopy (OM). Electrical, thermal, surface and crystalline properties of the spun fibers were evaluated, respectively, by conductivity measurements (4-point probe), thermogravimetric analyses (TGA), differential scanning calorimetry (DSC), contact angle and X-ray diffraction (XRD). OM analysis of the spun mats showed a poor dispersion of MWCNT in the matrix, however dispersion in solution was increased during spinning where droplets of PLA in solution loaded with MWCNT were pulled by the pressure drop at the nozzle, producing PLA fibers filled with MWCNT. Good electrical conductivity and hydrophobicity can be achieved at low carbon nanotube contents. When only 1 wt% MWCNT was added to low-crystalline PLA, surface conductivity of the composites increased from 5 x 10(-8) to 0.46 S/cm. Addition of MWCNT can slightly influence the degree of crystallinity of PLA fibers as studied by XRD and DSC. Thermogravimetric analyses showed that MWCNT loading can decrease the onset degradation temperature of the composites which was attributed to the catalytic effect of metallic residues in MWCNT. Moreover, it was demonstrated that hydrophilicity slightly increased with an increase in MWCNT content. These results show that solution blow spinning can also be used to produce nanocomposite fibers with many potential applications such as in sensors and biosensors. PMID:22755116

  20. Olfactory discrimination of structurally similar alcohols by cockroaches.

    PubMed

    Sakura, M; Okada, R; Mizunami, M

    2002-11-01

    The capability of the cockroach Periplaneta americana to discriminate odors of structurally similar aliphatic alcohols was studied by using an operant conditioning paradigm. Cockroaches were trained to discriminate three odors: one odor associated with sucrose solution (reward) and two odors associated with NaCl solution (non-reward). After training, their odor preferences were tested by counting the number of visits to each odor source. We tested the capability of cockroaches to discriminate (1) three normal aliphatic alcohols with different numbers of carbon (1-pentanol, 1-hexanol and 1-octanol), (2) three C6 aliphatic alcohols (1-hexanol, 2-hexanol and trans-2-hexen-1-ol), (3) binary mixtures of two of these three alcohols and their components, and (4) 1-hexanol solution of three different concentrations (1, 10 and 100 micro g micro l(-1)). Cockroaches exhibited higher preferences for the odors associated with reward in these tests, and we therefore conclude that cockroaches can discriminate these odors. However, discrimination of 1-hexanol and trans-2-hexen-1-ol and their binary mixture was imperfect, in that some statistical tests suggested significant level of discrimination but other tests did not. In addition, the cockroaches learned to associate a 1-hexanol solution of the highest or lowest concentration with sucrose reward but failed to learn to associate 1-hexanol of an intermediate concentration with reward. PMID:12466954

  1. Chemical and structural evaluation of activated carbon prepared from jute sticks for Brilliant Green dye removal from aqueous solution.

    PubMed

    Asadullah, Mohammad; Asaduzzaman, Mohammad; Kabir, Mohammad Shajahan; Mostofa, Mohammad Golam; Miyazawa, Tomohisa

    2010-02-15

    Activated carbons have been prepared from jute sticks by chemical activation using ZnCl(2) and physical activation using steam for the removal of Brilliant Green dye from aqueous solution. The activated carbons and charcoal prepared from jute sticks were characterized by evaluating the surface chemistry, structural features and surface morphology. The maximum BET surface area was obtained to be 2304 m(2)/g for chemical activated carbon (ACC) while it is 730 and 80 m(2)/g for steam activated carbon (ACS) and charcoal, respectively. The FT-IR spectra exhibited that the pyrolysis and steam activation of jute sticks resulted in the release of aliphatic and O-containing functional groups by thermal effect. However, the release of functional groups is the effect of chemical reaction in the ZnCl(2) activation process. A honeycomb-type carbon structure in ACC was formed as observed on SEM images. Although charcoal and ACC were prepared at 500 degrees C the ACC exhibited much lower Raman sensitivity due to the formation of condensed aromatic ring systems. Due to high surface area and high porous structure with abundance of functional groups, the ACC adsorbed dye molecules with much higher efficiency than those of ACS and charcoal. PMID:19815339

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

    PubMed

    Sayğılı, Hasan; Güzel, Fuat

    2016-09-01

    Activated carbon (TAC) prepared under optimized conditions with ZnCl2 activation from a new precursor; tomato industrial processing waste (TW), was applied as an adsorbent to remove tetracycline (TC) from aqueous solution. The factors (TAC dosage, initial TC concentration, contact time, ionic strength and solution temperature) affecting the adsorption process were examined at natural pH (5.7) of TAC-TC system in aqueous solution. Kinetic data was found to be best complied by the pseudo-second order model. The isotherm analysis indicated that the equilibrium data could be represented by the Langmuir model. The maximum adsorption capacity was identified as 500.0mgg(-1) at 308K. PMID:27177317

  3. The microwave assisted synthesis of 1-alkyl-3-methylimidazolium bromide as potential corrosion inhibitor toward carbon steel in 1 M HCl solution saturated with carbon dioxide

    NASA Astrophysics Data System (ADS)

    Pasasa, Norman Vincent A.; Bundjali, Bunbun; Wahyuningrum, Deana

    2015-09-01

    Injection of corrosion inhibitor into the fluid current of oil and gas pipelines is an effective way to mitigate corrosion rate on the inner-surface parts of pipelines, especially carbon steel pipelines. In this research, two alkylimidazolium ionic liquids, 1-decyl-3-methylimidazolium bromide (IL1) and 1-dodecyl-3-methylimidazolium bromide (IL2) have been synthesized and studied as a potential corrosion inhibitor towards carbon steel in 1 M HCl solution saturated with carbon dioxide. IL1 and IL2 were synthesized using microwave assisted organic synthesis (MAOS) method. Mass Spectrometry analysis of IL1 and IL2 showed molecular mass [M-H+] peak at 223.2166 and 251.2484, respectively. The FTIR,1H-NMR and 13C-NMR spectra confirmed that IL1 and IL2 were successfully synthesized. Corrosion inhibition activity of IL1 and IL2 were determined using weight loss method. The results showed that IL1 and IL2 have the potential as good corrosion inhibitors with corrosion inhibition efficiency of IL1 and IL2 are 96.00% at 100 ppm (343 K) and 95.60% at 50 ppm (343 K), respectively. The increase in the concentration of IL1 and IL2 tends to improve their corrosion inhibition activities. Analysis of the data obtained from the weight loss method shows that the adsorption of IL1 and IL2 on carbon steel is classified into chemisorption which obeys Langmuir's adsorption isotherm.

  4. 2, 4 dichlorophenol (2, 4-DCP) sorption from aqueous solution using granular activated carbon and polymeric adsorbents and studies on effect of temperature on activated carbon adsorption.

    PubMed

    Ghatbandhe, A S; Yenkie, M K N

    2008-04-01

    Adsorption equilibrium, kinetics and thermodynamics of 2,4-dichlorophenol (2,4-DCP), one of the most commonly used chlorophenol, onto bituminous coal based Filtrasorb-400 grade granular activated carbon, were studied in aqueous solution in a batch system with respect to temperature. Uptake capacity of activated carbon found to increase with temperature. Langmuir isotherm models were applied to experimental equilibrium data of 2, 4-DCP adsorption and competitive studies with respect to XAD resin were carried out. Equilibrium data fitted very well to the Langmuir equilibrium model. Adsorbent monolayer capacity 'Q0, Langmuir constant 'b' and adsorption rate constant 'k(a)' were evaluated at different temperatures for activated carbon adsorption. This data was then used to calculate the energy of activation of adsorption and also the thermodynamic parameters, namely the free energy of adsorption, deltaG0, enthalpy of adsorption, deltaH0 and the entropy of adsorption deltaS0. The obtained results showed that the monolayer capacity increases with the increase in temperatures. The obtained values of thermodynamic parameters showed that adsorption of 2,4 DCP is an endothermic process. Synthetic resin was not found efficient to adsorb 2,4 DCP compared to activated carbon. The order of adsorption efficiencies of three resins used in the study found as XAD7HP > XAD4 > XAD1180. PMID:19295102

  5. Propyl alcohol

    MedlinePlus

    Rubbing alcohol Alcohol swabs Skin and hair products Nail polish remover Note: This list may not be all ... number will let you talk to experts in poisoning. They will give you further instructions. This is ...

  6. Tetrahydrofuran-induced K and Li doping onto poly(furfuryl alcohol)-derived activated carbon (PFAC): Influence on microstructure and H2 sorption properties

    SciTech Connect

    Saha, Dipendu; Contescu, Cristian I; Gallego, Nidia C

    2012-01-01

    We have doped polyfurfuryl alcohol derived activated carbon (PFAC) with two alkali metals, potassium (K) and lithium (Li) by prior reacting the metals with naphthalene in presence of tetrahydrofuran (THF) followed by introducing them to pristine PFAC. THF molecule causes minor alteration in the microstructure of PFAC as confirmed by the Raman spectra, X-ray diffraction and pore textural analysis. Raman spectra and X-ray diffraction indicated a slight localized ordering towards the stacking defects of disordered carbon, like PFAC which can be attributed to the movement of THF molecules within the internal planes of graphene sheets. Pore textural analysis confirmed the lowering specific surface area and pore volume of both K and Li doped PFACs.(BET SSA: 1378 m2/g (PFAC); 1252 m2/g (K-PFAC); 1081 m2/g (Li-PFAC)) Volumetric hydrogen adsorption measurement at the temperatures of 298, 288, 273 and 77 K and pressure up to 1 bar indicated the enhanced adsorption potential imposed by the presence of alkali metals, which can be reconfirmed by the additional heats of adsorption of metal doped PFACs (Li-PFAC: -(10 - 11) kJ/mol; K-PFAC: -(16 -19) kJ/mol) compared to pristine PFAC (-9.6 kJ/mol).

  7. Removal of cationic heavy metal from aqueous solution by activated carbon impregnated with anionic surfactants.

    PubMed

    Ahn, Chi K; Park, Donghee; Woo, Seung H; Park, Jong M

    2009-05-30

    To increase their capacity to adsorb heavy metals, activated carbons were impregnated with the anionic surfactants sodium dodecyl sulfate (SDS), sodium dodecyl benzene sulfonate (SDBS), or dioctyl sulfosuccinate sodium (DSS). Surfactant-impregnated activated carbons removed Cd(II) at up to 0.198 mmol g(-1), which was more than an order of magnitude better than the Cd(II) removal performance of activated carbon without surfactant (i.e., 0.016 mmol g(-1)) even at optimal pH (i.e., pH 6). The capacity of the activated carbon to adsorb Cd(II) increased in proportion to the quantity of surfactant with which they were impregnated. The kinetics of the adsorption of Cd(II) onto the surfactant-impregnated activated carbon was best described by a pseudo-second-order model, and was described better by the Freundlich adsorption isotherm than by the Langmuir isotherm. The surface charge of activated carbon was negative in all pH ranges tested (2-6). These results indicate that surface modification with anionic surfactant could be used to significantly enhance the capacity of activated carbon to adsorb cations. PMID:19022570

  8. Alcoholic hallucinosis.

    PubMed

    Bhat, Pookala S; Ryali, Vssr; Srivastava, Kalpana; Kumar, Shashi R; Prakash, Jyoti; Singal, Ankit

    2012-07-01

    Alcoholic hallucinosis is a rare complication of chronic alcohol abuse characterized by predominantly auditory hallucinations that occur either during or after a period of heavy alcohol consumption. Bleuler (1916) termed the condition as alcohol hallucinosis and differentiated it from Delirium Tremens. Usually it presents with acoustic verbal hallucinations, delusions and mood disturbances arising in clear consciousness and sometimes may progress to a chronic form mimicking schizophrenia. One such case with multimodal hallucinations in a Defence Service Corps soldier is presented here. PMID:24250051

  9. Thermodynamic Control of the Isotope Composition of Divalent Metal Cations in Aqueous Solutions and in Carbonate Minerals

    NASA Astrophysics Data System (ADS)

    Schott, J.; Mavromatis, V.; Pearce, C. R.; Fujii, T.; Oelkers, E. H.

    2014-12-01

    The very contrasting steric and electronic properties of divalent metals dramatically affect the reactivity and composition of their aqueous species and their partitioning between fluids and minerals. These contrasting properties result also in very distinct kinetic and thermodynamic trends of their isotopic composition in aqueous fluids and carbonate minerals. For example, if alkaline earths in calcite are all enriched in light isotopes, only Mg exhibits a decrease of its isotope fractionation with increasing calcite growth rate. Moreover, the Mg2+ aquo ion is the only alkaline earth ion whose isotopic composition is markedly affected by the presence in solution of inorganic ligands like bicarbonate, carbonate or sulfate. The distinct behavior of Mg stems from the reduced lability of water molecules in its coordination sphere and from the reduction of its aquo ion coordination sphere when it coordinates to HCO3- and CO32-. Ab initio calculations show that the preferred four hydration number of Mg in stable Mg bicarbonate and Mg carbonate monomers results in a strong enrichment in 26Mg of these species compared to Mg(H2O)62+ (i.e. 1000lnβ26/24MgCO3°-1000lnβ26/24Mg2+ = 5.16 ‰; Fujii, personal communication). The analysis of recent experiments on Mg isotope fractionation between carbonate crystals and solution using density functionnal theory estimation of lnβ values from Fujii i) confirm the marked impact of carbonate and bicarbonate ligands on the isotope composition of Mg in calcite and magnesite and ii) allow to reconcile First-principles and experimental estimates of equilibrium Mg isotope fractionation in carbonate crystals. Recent experiments also confirm that the strong affinity of Zn2+ or Cu2+ for RO- ligands results in a marked impact of fluid pH, ΣCO2(aq) and/or carboxylic ligands concentrations on the isotope composition of these metals in carbonate minerals. These observations provide new insights into the parameters controlling the isotope

  10. Alcohol Abuse

    ERIC Educational Resources Information Center

    O'Farrell, Timothy J.; Fals-Stewart, William

    2003-01-01

    We received 38 controlled studies of marital and family therapy (MFT) in alcoholism treatment. We conclude that, when the alcoholic is unwilling to seek help, MFT is effective in helping the family cope better and motivating alcoholics to enter treatment. Specifically, (a) Al-Anon facilitation and referral help family members cope better; (b)…

  11. Catalytic Transfer Hydrogenation of Furfural to Furfuryl Alcohol over Nitrogen-Doped Carbon-Supported Iron Catalysts.

    PubMed

    Li, Jiang; Liu, Jun-Ling; Zhou, Hong-Jun; Fu, Yao

    2016-06-01

    Iron-based heterogeneous catalysts, which were generally prepared by pyrolysis of iron complexes on supports at elevated temperature, were found to be capable of catalyzing the transfer hydrogenation of furfural (FF) to furfuryl alcohol (FFA). The effects of metal precursor, nitrogen precursor, pyrolysis temperature, and support on catalytic performance were examined thoroughly, and a comprehensive study of the reaction parameters was also performed. The highest selectivity of FFA reached 83.0 % with a FF conversion of 91.6 % under the optimal reaction condition. Catalyst characterization suggested that iron cations coordinated by pyridinic nitrogen functionalities were responsible for the enhanced catalytic activity. The iron catalyst could be recycled without significant loss of catalytic activity for five runs, and the destruction of the nitrogen-iron species, the presence of crystallized Fe2 O3 phase, and the pore structure change were the main reasons for catalyst deactivation. PMID:27144965

  12. Junction-Controlled Elasticity of Single-Walled Carbon Nanotube Dispersions in Acrylic Copolymer Gels and Solutions

    SciTech Connect

    Schoch, Andrew B.; Shull, Kenneth R.; Brinson, L. Catherine

    2008-08-26

    Oscillatory shear rheometry is used to study the mechanical response of single-walled carbon nanotubes dispersed in solutions of acrylic diblock or triblock copolymers in 2-ethyl-1-hexanol. Thermal transitions in the copolymer solutions provide a route for the easy processing of these composite materials, with excellent dispersion of the nanotubes as verified by near-infrared photoluminescence spectroscopy. The nanotube dispersions form elastic networks with properties that are controlled by the junction points between nanotubes, featuring a temperature-dependent elastic response that is controlled by the dynamic properties of the matrix copolymer solution. The data are consistent with the formation of micelle-like aggregates around the nanotubes. At low temperatures the core-forming poly(methyl methacrylate) blocks are glassy, and the overall mechanical response of the composite does not evolve with time. At higher temperatures the enhanced mobility of the core-forming blocks enables the junctions to achieve more intimate nanotube-nanotube contact, and the composite modulus increases with time. These aging effects are observed in both diblock and triblock copolymer solutions but are partially reversed in the triblock solutions by cooling through the gel transition of the triblock copolymer. This result is attributed to the generation of internal stresses during gelation and the ability of these stresses to break or weaken the nanotube junctions.

  13. Activated carbons from coal/pitch and polyethylene terephthalate blends for the removal of phenols from aqueous solutions

    SciTech Connect

    Ewa Lorenc-Grabowska; Grazyna Gryglewicz; Jacek Machnikowski

    2009-05-15

    Blends of two bituminous coals and a coal-tar pitch (CTP) with polyethylene terephthalate (PET) were evaluated as precursors of activated carbons (ACs). The intensity of the interactions between the raw materials, coal/CTP and PET during copyrolysis was closely observed by means of thermogravimetric analysis. In addition, the homogeneity of the carbon matrix of the chars produced at 800{sup o}C in a horizontal oven was studied by polarized light optical microscopy. Activated carbons were prepared from single components and their blends (1:1 w/w) by subjecting them to carbonization up to 800{sup o}C in a horizontal oven and then activation with steam at 800{sup o}C to 50% burnoff. The porous structure of the ACs was determined by sorption of N{sub 2} at 77 K and of CO{sub 2} at 273 K. The PET-containing blends produced microporous activated carbons with a maximum BET surface area of nearly 1100 m{sup 2} g{sup -1} and a maximum micropore size distribution of 0.6-0.8 nm in the case of the AC from the CTP/PET blend. The addition of PET to a bituminous coal was compared with the preoxidation of coal P in air as a way to reduce thermoplasticity and to promote the development of the porous structure. The modification of bituminous coals by PET appeared to be more effective than conventional coal preoxidation treatment. The resultant ACs were tested by measuring their effectiveness in removing phenols from an aqueous solution. The adsorption of p-chlorophenol (PCP) by the ACs prepared from the PET-containing blends was slightly higher than for the commercial activated carbon. The ability to adsorb PCP was found to be related to the volume of the super-micropores.

  14. Facts about Alcohol and Alcoholism.

    ERIC Educational Resources Information Center

    Hall, Leonard C.

    Recognition of alcoholism as a treatable illness is a result of public education based on scientific facts. This publication, a digest of a more detailed survey of research about drinking and alcoholism, presents information about alcohol and its effects on individuals and society. It provides facts about the short-term and long-term effects of…

  15. Alcoholic cardiomyopathy

    PubMed Central

    Guzzo-Merello, Gonzalo; Cobo-Marcos, Marta; Gallego-Delgado, Maria; Garcia-Pavia, Pablo

    2014-01-01

    Alcohol is the most frequently consumed toxic substance in the world. Low to moderate daily intake of alcohol has been shown to have beneficial effects on the cardiovascular system. In contrast, exposure to high levels of alcohol for a long period could lead to progressive cardiac dysfunction and heart failure. Cardiac dysfunction associated with chronic and excessive alcohol intake is a specific cardiac disease known as alcoholic cardiomyopathy (ACM). In spite of its clinical importance, data on ACM and how alcohol damages the heart are limited. In this review, we evaluate available evidence linking excessive alcohol consumption with heart failure and dilated cardiomyopathy. Additionally, we discuss the clinical presentation, prognosis and treatment of ACM. PMID:25228956

  16. Cutoff in potency implicates alcohol inhibition of N-methyl-D-aspartate receptors in alcohol intoxication.

    PubMed Central

    Peoples, R W; Weight, F F

    1995-01-01

    As the number of carbon atoms in an aliphatic n-alcohol is increased from one to five, intoxicating potency, lipid solubility, and membrane lipid disordering potency all increase in a similar exponential manner. However, the potency of aliphatic n-alcohols for producing intoxication reaches a maximum at six to eight carbon atoms and then decreases. The molecular basis of this "cutoff" effect is not understood, as it is not correlated with either the lipid solubility or the membrane disordering potency of the alcohols, which continue to increase exponentially. Since it has been suggested that inhibition of N-methyl-D-aspartate (NMDA) receptors by alcohols may play a role in alcohol intoxication, we investigated whether a series of aliphatic n-alcohols would exhibit a cutoff in potency for inhibition of NMDA receptors. We found that although potency for inhibition of NMDA receptors increased exponentially for alcohols with one to five carbon atoms, potency for inhibition of NMDA receptors reached a maximum at six to eight carbon atoms and then abruptly disappeared. This cutoff for alcohol inhibition of NMDA receptors is consistent with an interaction of the alcohols with a hydrophobic pocket on the receptor protein. In addition, the similarity of the cutoffs for alcohol inhibition of NMDA receptors and alcohol intoxication suggests that the cutoff for NMDA receptor inhibition may contribute to the cutoff for alcohol intoxication, which is consistent with an important role of NMDA receptors in alcohol intoxication. PMID:7708732

  17. Interactions between viruses and goethite during saturated flow: effects of solution pH, carbonate, and phosphate.

    PubMed

    Zhuang, Jie; Jin, Yan

    2008-05-26

    Metal oxides have great potential for controlling the fate and transport of viruses in the subsurface and water-treatment systems. The processes, however, are subject to solution chemistry. In this study, a number of column experiments were conducted to examine the effects of solution pH and anions (carbonate and phosphate) on attachment, transport, and inactivation of two bacteriophages (phiX174 and MS-2) in goethite-coated sand medium. Removal of both viruses on goethite-coated sand increased as solution pH decreased from 9.3 to 7.5, due mostly to virus inactivation. MS-2, a relatively hydrophobic virus with a lower isoelectric point (3.9), was more sensitive to the change of solution pH than phiX174, a relatively hydrophilic virus with a higher isoelectric point (6.6), in terms of their attachment and inactivation on goethite. About 90% of the MS-2 particles removed by goethite (accounting for 81% of the total input) were inactivated at pH 7.5, whereas all of the removed MS-2 particles (accounting for 10% of the total input) still remained infectious at pH 9.3. In comparison, approximately 74% of the goethite-bound phiX174 particles (accounting for 95% of the total input) lost their infectivity at pH 7.5, in contrast to a complete recovery at pH 9.3 (accounting for 65% of the total input) when the columns were eluted using a beef extract solution (pH 9.5). Presence of phosphate (20 mM H(2)PO(4)(-)) in input solution reduced virus attachment and appeared to protect the viruses from being inactivated during transport; this effect was more significant on MS-2 than on phiX174. Specifically, approximately 29% of the phiX174 particles and approximately 49% of MS-2 particles injected into the column were removed during transport. Mass recovery data showed that no phiX174 was inactivated in the presence of phosphate, whereas about 38% of the MS-2 particles attached on goethite lost their infectivity. Conversely, presence of carbonate on goethite increased virus

  18. Two competitive nucleation mechanisms of calcium carbonate biomineralization in response to surface functionality in low calcium ion concentration solution

    PubMed Central

    Deng, Hua; Wang, Shuo; Wang, Xiumei; Du, Chang; Shen, Xingcan; Wang, Yingjun; Cui, Fuzhai

    2015-01-01

    Four self-assembled monolayer surfaces terminated with –COOH, –OH, –NH2 and –CH3 functional groups are used to direct the biomineralization processes of calcium carbonate (CaCO3) in low Ca2+ concentration, and the mechanism of nucleation and initial crystallization within 12 h was further explored. On −COOH surface, nucleation occurs mainly via ion aggregation mechanism while prenucleation ions clusters may be also involved. On −OH and −NH2 surfaces, however, nucleation forms via calcium carbonate clusters, which aggregate in solution and then are adsorbed onto surfaces following with nucleation of amorphous calcium carbonate (ACC). Furthermore, strongly negative-charged −COOH surface facilitates the direct formation of calcites, and the −OH and −NH2 surfaces determine the formation of vaterites with preferred crystalline orientations. Neither ACC nor crystalline CaCO3 is observed on −CH3 surface. Our findings present a valuable model to understand the CaCO3 biomineralization pathway in natural system where functional groups composition plays a determining role during calcium carbonate crystallization. PMID:26814639

  19. Two competitive nucleation mechanisms of calcium carbonate biomineralization in response to surface functionality in low calcium ion concentration solution.

    PubMed

    Deng, Hua; Wang, Shuo; Wang, Xiumei; Du, Chang; Shen, Xingcan; Wang, Yingjun; Cui, Fuzhai

    2015-09-01

    Four self-assembled monolayer surfaces terminated with -COOH, -OH, -NH2 and -CH3 functional groups are used to direct the biomineralization processes of calcium carbonate (CaCO3) in low Ca(2+) concentration, and the mechanism of nucleation and initial crystallization within 12 h was further explored. On -COOH surface, nucleation occurs mainly via ion aggregation mechanism while prenucleation ions clusters may be also involved. On -OH and -NH2 surfaces, however, nucleation forms via calcium carbonate clusters, which aggregate in solution and then are adsorbed onto surfaces following with nucleation of amorphous calcium carbonate (ACC). Furthermore, strongly negative-charged -COOH surface facilitates the direct formation of calcites, and the -OH and -NH2 surfaces determine the formation of vaterites with preferred crystalline orientations. Neither ACC nor crystalline CaCO3 is observed on -CH3 surface. Our findings present a valuable model to understand the CaCO3 biomineralization pathway in natural system where functional groups composition plays a determining role during calcium carbonate crystallization. PMID:26814639

  20. Study On Adsorption of Bromate From Aqueous Solution On Modified Activated Carbon

    NASA Astrophysics Data System (ADS)

    Liu, Tong-mian; Cui, Fu-yi; Zhao, Zhi-wei; Liu, Dong-mei; Zhu, Qi; Wang, Huan

    2010-11-01

    A coal-based activated carbon was treated chemically with nitric acid, sodium hydroxide and ammonia for its surface modification, and its adsorption capacity was investigated with bromate. Several techniques were used to characterize the physicochemical properties of these materials including BET, XPS, pHpzc and Boehm titration. The results indicated that the specific surface area of the activated carbon decreased after oxidation with nitric acid. But the amount of surface acidic oxygen-containing functional groups of the oxidized sample increased compared to the raw carbon and the points of zero charge (pHpzc) decreased. The specific surface area of the activated carbon also decreased after sodium hydroxide treatment and the points of zero charge increased. The changes of surface chemical properties after the ammonia treatment was opposite to the oxidized sample. As a result, the pHpzc of the carbon was increased to near pH9.3, the amount of surface basic groups was increased. Furthermore, the data of bromate adsorption on all the samples were fitted to the Langmuir isotherm model well which indicates monolayer adsorption. In addition, the adsorption capacity of ammonia treatment sample was the highest and its saturated adsorption capacity reached 1.55 mg/g. A strong correlation was found between basic groups and adsorption capacity of bromate. Enhancement of basic groups was favorable for bromate removal.