Sample records for alkalis hydroxides

  1. Hydrogen storage over alkali metal hydride and alkali metal hydroxide composites

    Institute of Scientific and Technical Information of China (English)

    Pei Yu; Yong Shen Chua; Hujun Cao; Zhitao Xiong; Guotao Wu; Ping Chen


    Alkali metal hydroxide and hydride composite systems contain both protic (H bonded with O) and hydridic hydrogen. The interaction of these two types of hydrides produces hydrogen. The enthalpy of dehydrogenation increased with the increase of atomic number of alkali metals, i.e.,-23 kJ/molH2 for LiOH-LiH, 55.34 kJ/molH2 for NaOH-NaH and 222 kJ/molH2 for KOH-KH. These thermodynamic calculation results were consistent with our experimental results. H2 was released from LiOH-LiH system during ball milling. The dehydrogenation temperature of NaOH-NaH system was about 150◦C; whereas KOH and KH did not interact with each other during the heating process. Instead, KH decomposed by itself. In these three systems, NaOH-NaH was the only reversible hydrogen storage system, the enthalpy of dehydrogenation was about 55.65 kJ/molH2 , and the corresponding entropy was ca. 101.23 J/(molH2 ·K), so the temperature for releasing 1.0 bar H2 was as high as 518◦C, showing unfavorable thermodynamic properties. The activation energy for hydrogen desorption of NaOH-NaH was found to be 57.87 kJ/mol, showing good kinetic properties.

  2. Structure and properties of alizarin complex formed with alkali metal hydroxides in methanol solution. (United States)

    Jeliński, Tomasz; Cysewski, Piotr


    Quantum chemical computations were used for prediction of the structure and color of alizarin complex with alkali metal hydroxides in methanolic solutions. The color prediction relying on the single Gaussian-like band once again proved the usefulness of the PBE0 density functional due to the observed smallest color difference between computed and experimentally derived values. It was found that the alkali metal hydroxide molecules can bind to the two oxygen atoms of both hydroxyl groups of alizarin or to one of these atoms and the oxygen atom from the keto group in a complex with three methanol molecules. This means that two electronic transitions need to be taken into account when considering the spectra of the studied complexes. The resulting bond lengths and angles are correlated with the properties of the alkali metal atoms. The molar mass, the atomic radius, and the Pauling electronegativity of studied metals are quite accurate predictors of the geometric properties of hydroxide complexes with alizarin in methanol solution. Graphical abstract The spectra of the neutral and monoanionic form of alizarin together with color changes resulting from addition of different metal hydroxides and represented in CIE color space.


    Directory of Open Access Journals (Sweden)

    Sami ŞAHİN


    Full Text Available At present more than 90 per cent of the world's alumina is produced by the Bayer process, a simple technology providing high purity final product. A part from some exceptional local conditions, bauxite is processed almost solely by this technology. As a benefication process, alumina production releases the aluminum oxide content of bauxite from other accompanying oxides thus providing alumina suitable for electrolysis in a cryolite melt. The basic theory of the Bayer process was elaborated by K.J. Bayer and described in his patents in 1887 and 1892. The first patent refers to the aid of seed crystals of aluminum hydroxide or of carbonic acid, that is, to the precipitation and carbonation processes. The second patent formulates the concept that the aluminum oxide content of bauxites can be dissolved in sodium hydroxide solutions, with the formulation of sodium aluminate, a process called digestion nowadays. The most important operations of the Bayer technology are bauxite preparation, crushing, grinding, digestion, red mud separation, thickening, washing, filtration, precipitation, calcination and evaporation. In spite of its great significance as regards the complete Bayer technology, the structure of sodium aluminate solutions has not been cleared up definitely yet. Boehmite is the most important aluminum mineral of karstic bauxites. Some experimental results showing the various effects on aluminum hydroxides by alkali process from boehmitic bauxites and the factors gowerning the digestion operation of aluminate solutions were investigated.

  4. Structural properties and adsorption capacity of holocellulose aerogels synthesized from an alkali hydroxide-urea solution

    Energy Technology Data Exchange (ETDEWEB)

    Kwon, Gu-Joong; Kim, Dae-Young; Hwang, Jae-Hyun; Kang, Joo-Hyon [Dongguk University, Seoul (Korea, Republic of)


    A tulip tree was used to synthesize a holocellulose aerogel from an aqueous alkali hydroxide-urea solution with the substitution of an organic solvent followed by freeze-drying. For comparison, the synthesized holocellulose aerogels were divided into two groups according to the source of the hydrogel, an upper suspended layer and a bottom concentrated layer of the centrifuged solution of cellulose and NaOH/urea solvents. We investigated the effects of the temperature of the pre-cooled NaOH/urea solution (i.e., dissolution temperature) on the pore structure and the adsorption capacity of the holocellulose aerogel. A nano-fibrillar network structure of the holocellulose aerogel was observed, with little morphological difference in pore structure for different dissolution temperatures. Both micropores and mesopores were observed in the holocellulose aerogel. The specific surface area of the holocellulose aerogel was generally greater at lower dissolution temperatures. In a series of adsorption tests using methylene blue, the holocellulose aerogel showed the greatest adsorption capacity at the lowest dissolution temperature tested ( -2 .deg. C). However, the dissolution temperature generally had little effect on the adsorption capacity. The holocellulose aerogel produced from the upper suspended layer of the centrifuged hydrogel solution showed a greater porosity and adsorption capacity than the one produced from the bottom concentrated layer. Overall, the aerogel made by utilizing a delignified tulip tree display a high surface area and a high adsorption property, indicating its possible application in eco-friendly adsorption materials.

  5. Magnesium alloys and graphite wastes encapsulated in cementitious materials: Reduction of galvanic corrosion using alkali hydroxide activated blast furnace slag. (United States)

    Chartier, D; Muzeau, B; Stefan, L; Sanchez-Canet, J; Monguillon, C


    Magnesium alloys and graphite from spent nuclear fuel have been stored together in La Hague plant. The packaging of these wastes is under consideration. These wastes could be mixed in a grout composed of industrially available cement (Portland, calcium aluminate…). Within the alkaline pore solution of these matrixes, magnesium alloys are imperfectly protected by a layer of Brucite resulting in a slow corrosion releasing hydrogen. As the production of this gas must be considered for the storage safety, and the quality of wasteform, it is important to select a cement matrix capable of lowering the corrosion kinetics. Many types of calcium based cements have been tested and most of them have caused strong hydrogen production when magnesium alloys and graphite are conditioned together because of galvanic corrosion. Exceptions are binders based on alkali hydroxide activated ground granulated blast furnace slag (BFS) which are presented in this article.

  6. Thermochemical analysis of laterite ore alkali roasting: Comparison of sodium carbonate, sodium sulfate, and sodium hydroxide (United States)

    Samadhi, Tjokorde Walmiki


    The abundance of global nickel reserve is in fact dominated by low grade laterite ores containing only approximately 1.0-1.8 %-Ni. Indonesia is a major limonite and saprolite ores source, particularly in the Sulawesi, northern Maluku, and Papua islands. Production of nickel from laterites typically requires a pre-concentration step which breaks down the mineral crystalline structure, thereby facilitating the subsequent extraction of the valuable metals. This work discusses the thermochemical analysis of the alkali roasting of an Indonesian saprolite ore using Na2CO3, Na2SO4, and NaOH. These alkali compounds are selected due to their relatively low cost. The Factsage thermochemical computation package is used to predict thermodynamically stable gaseous, solution, pure liquid, and pure solid phases present in the roasting process at temperatures from 100 to 1200°C at ambient pressure, in inert atmosphere. The formation of a liquid solution (or slag) phase is interpreted as a major indicator of mineral structure breakdown. The computed slag formation temperatures are 373.2, 1041.4, and 792.0°C when using Na2CO3, Na2SO4, and NaOH, respectively. The masses of volatilized alkali at 1200°C with a total feed mass of 100 gram are 0.49, 3.24, and 3.25 mg for Na2CO3, Na2SO4, and NaOH, respectively. It is therefore hypothesized that Na2CO3 is the most competitive sodium-based alkali for saprolite ore roasting.

  7. CO2 Extraction from Ambient Air Using Alkali-Metal Hydroxide Solutions Derived from Concrete Waste and Steel Slag (United States)

    Stolaroff, J. K.; Lowry, G. V.; Keith, D. W.


    To mitigate global climate change, deep reductions in CO2 emissions are required in the coming decades. Carbon sequestration will play a crucial role in this reduction. Early adoption of carbon sequestration in low-cost niche markets will help develop the technology and experience required for large-scale deployment. One such niche may be the use of alkali metals from industrial waste streams to form carbonate minerals, a safe and stable means of sequestering carbon. In this research, the potential of using two industrial waste streams---concrete and steel slag---for sequestering carbon is assessed. The scheme is outlined as follows: Ca and Mg are leached with water from a finely ground bed of steel slag or concrete. The resulting solution is sprayed through air, capturing CO2 and forming solid carbonates, and collected. The feasibility of this scheme is explored with a combination of experiments, theoretical calculations, cost accounting, and literature review. The dissolution kinetics of steel slag and concrete as a function of particle size and pH is examined. In stirred batch reactors, the majority of Ca which dissolved did so within the first hour, yielding between 50 and 250 (mg; Ca)/(g; slag) and between 10 and 30 (mg; Ca)/(g; concrete). The kinetics of dissolution are thus taken to be sufficiently fast to support the type of scheme described above. As proof-of-concept, further experiments were performed where water was dripped slowly through a stagnant column of slag or concrete and collected at the bottom. Leachate Ca concentrations in the range of 15 mM were achieved --- sufficient to support the scheme. Using basic physical principles and numerical methods, the quantity of CO2 captured by falling droplets is estimated. Proportion of water loss and required pumping energy is similarly estimated. The results indicate that sprays are capable of capturing CO2 from the air and that the water and energy requirements are tractable. An example system for

  8. Structures and heats of formation of simple alkali metal compounds: hydrides, chlorides, fluorides, hydroxides, and oxides for Li, Na, and K. (United States)

    Vasiliu, Monica; Li, Shenggang; Peterson, Kirk A; Feller, David; Gole, James L; Dixon, David A


    Geometry parameters, frequencies, heats of formation, and bond dissociation energies are predicted for simple alkali metal compounds (hydrides, chlorides, fluorides, hydroxides and oxides) of Li, Na, and K from coupled cluster theory [CCSD(T)] calculations including core-valence correlation with the aug-cc-pwCVnZ basis set (n = D, T, Q, and 5). To accurately calculate the heats of formation, the following additional correction were included: scalar relativistic effects, atomic spin-orbit effects, and vibrational zero-point energies. For calibration purposes, the properties of some of the lithium compounds were predicted with iterative triple and quadruple excitations via CCSDT and CCSDTQ. The calculated geometry parameters, frequencies, heats of formation, and bond dissociation energies were compared with all available experimental measurements and are in excellent agreement with high-quality experimental data. High-level calculations are required to correctly predict that K(2)O is linear and that the ground state of KO is (2)Sigma(+), not (2)Pi, as in LiO and NaO. This reliable and consistent set of calculated thermodynamic data is appropriate for use in combustion and atmospheric simulations.

  9. Structural changes of polyacids initiated by their neutralization with various alkali metal hydroxides. Diffusion studies in poly(acrylic acid)s. (United States)

    Masiak, Michal; Hyk, Wojciech; Stojek, Zbigniew; Ciszkowska, Malgorzata


    The changes in the three-dimensional structure of the poly(acrylic acid), PAA, induced by incorporation of various alkali-metal counterions have been evaluated by studying diffusion of an uncharged probe (1,1'-ferrocenedimethanol) in the polymeric media. The studies are supported by the measurements of conductivity and viscosity of the polymeric media. Solutions of linear PAA of four different sizes (molecular weights: 450,000, 750,000, 1,250,000, 4,000,000) were neutralized with hydroxides of alkali metals of group 1 of the periodic table (Li, Na, K, Rb, Cs) to the desired neutralization degree. The transport properties of the obtained polyacrylates were monitored by measuring the changes in the probe diffusion coefficient during the titration of the polyacids. The probe diffusivity was determined from the steady-state current of the probe voltammetric oxidation at disk microelectrodes. Diffusivity of the probe increases with the increase in the degree of neutralization and with the increase in viscosity. It reaches the maximum value at about 60-80% of the polyacid neutralization. The way the probe diffusion coefficients change is similar in all polyacid solutions and gels. The increase in the size of a metal cation causes, in general, an enhancement in the transport of probe molecules. The biggest differences in the probe diffusivities are between lithium and cesium polyacrylates. The differences between the results obtained for cesium and rubidium are not statistically significant due to lack of good precision of the voltammetric measurements. The measurements of the electric conductivity of polyacrylates and the theoretical predictions supplemented the picture of electrostatic interactions between the polyanionic chains and the metal cations of increasing size. In all instances of the PAAs, the viscosity of the solutions rapidly increases in the 0-60% range of neutralization and then becomes constant in the 60-100% region. With the exception of the shortest

  10. Magnesium Hydroxide (United States)

    Magnesium hydroxide is used on a short-term basis to treat constipation.This medication is sometimes prescribed ... Magnesium hydroxide come as a tablet and liquid to take by mouth. It usually is taken as ...

  11. Alkali-metal ion coordination in uranyl(VI) poly-peroxide complexes in solution. Part 1: the Li⁺, Na⁺ and K⁺--peroxide-hydroxide systems. (United States)

    Zanonato, Pier Luigi; Di Bernardo, Plinio; Vallet, Valerie; Szabó, Zoltán; Grenthe, Ingmar


    The alkali metal ions Li(+), Na(+) and K(+) have a profound influence on the stoichiometry of the complexes formed in uranyl(VI)-peroxide-hydroxide systems, presumably as a result of a templating effect, resulting in the formation of two complexes, M[(UO2)(O2)(OH)]2(-) where the uranyl units are linked by one peroxide bridge, μ-η(2)-η(2), with the second peroxide coordinated "end-on", η(2), to one of the uranyl groups, and M[(UO2)(O2)(OH)]4(3-), with a four-membered ring of uranyl ions linked by μ-η(2)-η(2) peroxide bridges. The stoichiometry and equilibrium constants for the reactions: M(+) + 2UO2(2+) + 2HO2(-) + 2H2O → M[(UO2)(O2)(OH)]2(-) + 4H(+) (1) and M(+) + 4UO2(2+) + 4HO2(-) + 4H2O → M[(UO2)(O2)(OH)]4(3-) + 8H(+) (2) have been measured at 25 °C in 0.10 M (tetramethyl ammonium/M(+))NO3 ionic media using reaction calorimetry. Both reactions are strongly enthalpy driven with large negative entropies of reaction; the observation that ΔH(2) ≈ 2ΔH(1) suggests that the enthalpy of reaction is approximately the same when peroxide is added in bridging and "end-on" positions. The thermodynamic driving force in the reactions is the formation of strong peroxide bridges and the role of M(+) cations is to provide a pathway with a low activation barrier between the reactants and in this way "guide" them to form peroxide bridged complexes; they play a similar role as in the synthesis of crown-ethers. Quantum chemical (QC) methods were used to determine the structure of the complexes, and to demonstrate how the size of the M(+)-ions affects their coordination geometry. There are several isomers of Na[(UO2)(O2)(OH)]2(-) and QC energy calculations show that the ones with a peroxide bridge are substantially more stable than the ones with hydroxide bridges. There are isomers with different coordination sites for Na(+) and the one with coordination to the peroxide bridge and two uranyl oxygen atoms is the most stable one.

  12. High effective silica fume alkali activator

    Indian Academy of Sciences (India)

    Vladimír Živica


    Growing demands on the engineering properties of cement based materials and the urgency to decrease unsuitable ecologic impact of Portland cement manufacturing represent significant motivation for the development of new cement corresponding to these aspects. One category represents prospective alkali activated cements. A significant factor influencing their properties is alkali activator used. In this paper we present a new high effective alkali activator prepared from silica fume and its effectiveness. According to the results obtained this activator seems to be more effective than currently used activators like natrium hydroxide, natrium carbonate, and water glass.

  13. Hydroxide depletion in dilute supernates stored in waste tanks

    Energy Technology Data Exchange (ETDEWEB)

    Hobbs, D.T.


    Free hydroxide ion in dilute supernates are depleted by reaction with atmospheric carbon dioxide to form bicarbonate and carbonate species and by reaction with acidic compounds formed by the radiolytic decomposition of tetraphenylborate salts. A model of the kinetics and thermodynamics of absorption of carbon dioxide in the waste tanks has been developed. Forecasts of the rate of hydroxide depletion and the requirements for sodium hydroxide to maintain technical standards have been made for the washed sludge and washed precipitate storage tanks. Hydroxide depletion is predicted to have a minimal impact on sludge processing operations. However, in-tank precipitation and downstream DWPF operations are predicted to be significantly affected by hydroxide depletion in Tank 49H. The installation of a carbon dioxide scrubber on Tank 49H may be justified in view of the decrease in alkali content and variation in the melter feed.

  14. Sodium hydroxide poisoning (United States)

    Sodium hydroxide is a very strong chemical. It is also known as lye and caustic soda. This ... poisoning from touching, breathing in (inhaling), or swallowing sodium hydroxide. This article is for information only. Do ...

  15. Photoionization in alkali lasers. (United States)

    Knize, R J; Zhdanov, B V; Shaffer, M K


    We have calculated photoionization rates in alkali lasers. The photoionization of alkali atoms in the gain medium of alkali lasers can significantly degrade the laser performance by reducing the neutral alkali density and with it the gain. For a ten atmosphere Rb laser and a Cs exciplex laser, the photoionization induced alkali atom loss rates are greater than 10(5) sec(-1). These high loss rates will quickly deplete the neutral alkali density, reducing gain, and may require fast, possibly, supersonic flow rates to sufficiently replenish the neutral medium for CW operation.

  16. Milk-alkali syndrome (United States)

    ... this page: // Milk-alkali syndrome To use the sharing features on this page, please enable JavaScript. Milk-alkali syndrome is a condition in which there ...

  17. Mechanical and physical characterization of sodium hydroxide treated Borassus fruit fibers

    Institute of Scientific and Technical Information of China (English)

    Obi Reddy K; Shukla M; Uma Maheswari C; Varada Rajulu A


    In order to improve the properties by chemical modification and to optimize the alkali concentration,we treated Borassus fruit fine fibers with aqueous sodium hydroxide solutions of different concentrations.In each case,the tensile properties of the fibers were determined.The morphology of the untreated and alkali treated fibers was observed using scanning electron microscope.The surface of the fibers became rough on alkali treatment.The tensile properties of the fibers improved on alkali treatment.The fibers attained maximum tensile properties when treated with 15% aqueous sodium hydroxide solution and decreased thereafter.The crystallinity index of the fibers showed a similar trend.The thermal stability of the alkali treated fibers was found to be higher than that of untreated fibers.Further,the char content was maximum for fibers treated with alkali having concentration of 15% and above.The chemical composition indicated that the percentageof α-cellulose was maximum when the fibers were treated with 15% aqueous sodium hydroxide solution and then decreased thereafter thus indicating the beginning of degradation of the fibers at higher concentrations.Thus,the optimum concentration of NaOH was established as 15% for alkali treatment of the Borassus fibers.

  18. Microstructure and Engineering Properties of Alkali Activated Fly Ash -as an environment friendly alternative to Portland cement

    NARCIS (Netherlands)

    Ma, Y.


    Alkali activated fly ash (AAFA), also named “geopolymer”, has emerged as a novel engineering material in the construction industry. This material is normally formed by the reaction between fly ash and aqueous hydroxide or alkali silicate solution. With proper mix design, AAFA can present comparable

  19. Utilization of Mineral Wools as Alkali-Activated Material Precursor

    Directory of Open Access Journals (Sweden)

    Juho Yliniemi


    Full Text Available Mineral wools are the most common insulation materials in buildings worldwide. However, mineral wool waste is often considered unrecyclable because of its fibrous nature and low density. In this paper, rock wool (RW and glass wool (GW were studied as alkali-activated material precursors without any additional co-binders. Both mineral wools were pulverized by a vibratory disc mill in order to remove the fibrous nature of the material. The pulverized mineral wools were then alkali-activated with a sodium aluminate solution. Compressive strengths of up to 30.0 MPa and 48.7 MPa were measured for RW and GW, respectively, with high flexural strengths measured for both (20.1 MPa for RW and 13.2 MPa for GW. The resulting alkali-activated matrix was a composite-type in which partly-dissolved fibers were dispersed. In addition to the amorphous material, sodium aluminate silicate hydroxide hydrate and magnesium aluminum hydroxide carbonate phases were identified in the alkali-activated RW samples. The only crystalline phase in the GW samples was sodium aluminum silicate. The results of this study show that mineral wool is a very promising raw material for alkali activation.

  20. Impact of Alkali Pretreatment on the Chemical Component Distribution and Ultrastructure of Poplar Cell Walls


    Zhe Ji; Zhe Ling; Xun Zhang; Gui-Hua Yang; Feng Xu


    Alkali pretreatment is one of the leading pretreatment technologies for biofuel applications. The histochemical and structural characteristics of poplar cell walls were investigated before and after sodium hydroxide pretreatment (121 oC, 2%) to understand the alterations in biomass cellular structure, which were correlated with saccharification yield. Results showed that alkali pretreatment preferentially removed lignin from the S2 of fibers, which was similar to the behaviors of coniferyl al...

  1. Properties of Hooked Steel Fibers Reinforced Alkali Activated Material Concrete

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    Faris M. A.


    Full Text Available In this study, alkali activated material was produced by using Class F fly ash from Manjung power station, Lumut, Perak, Malaysia. Fly ash then was activated by alkaline activator which is consisting of sodium silicate (Na2SiO3 and sodium hydroxide (NaOH. Hooked end steel fibers were added into the alkali activated material system with percentage vary from 0 % – 5 %. Chemical compositions of fly ash were first analyzed by using x-ray fluorescence (XRF. All hardened alkali activated material samples were tested for density, workability, and compression after 28 days. Results show a slight increase of density with the addition of steel fibers. However, the workability was reduced with the addition of steel fibers content. Meanwhile, the addition of steel fibers shows the improvement of compressive strength which is about 19 % obtained at 3 % of steel fibers addition.

  2. Process optimization of reaction of acid leaching residue of asbestos tailing and sodium hydroxide aqueous solution

    Institute of Scientific and Technical Information of China (English)


    Silica is the major component of the acid leaching residue of asbestos tailing. The waterglass solution can be prepared by the reaction of the residue with sodium hydroxide aqueous solution. Compared to the high temperature reaction method, this process is environmental friendly and low cost. In this paper, the reaction process of the residue and the sodium hydroxide aqueous solution is optimized. The optimum reaction process parameters are as follows: the usage of sodium hydroxide is 26.4 g/100 g acid leaching residue, the reaction temperature is 90℃, the reaction time is 1 h, and the ratio of the liquid/solid is 2.0. The significance sequence of the process parameters to the alkali leaching reaction effect is the usage of sodium hydroxide > the ratio of the liquid/solid > the reaction time > the reaction temperature. The significance sequence to the leaching ratio of SiO2 is the ratio of the liquid/solid > the usage of sodium hydroxide > the reaction time > the reaction temperature. The significance sequence to the modulus of the sodium silicate is the ratio of the liquid/solid > the usage of sodium hydroxide > the reaction time > the reaction temperature. Under the optimum conditions, the leaching ratio of the SiO2 is 77.5%, and the modulus of the sodium silicate is 3.15. The XRD analysis result indicates that the major components of the alkali leaching residue are serpentine, talc, quartz and some albite.


    DEFF Research Database (Denmark)


    The present invention concerns the selective removal of nitrogen oxides (NOx) from gasses. In particular, the invention concerns a process, a catalyst and the use of a catalyst for the selective removal of nitrogen oxides in the presence of ammonia from gases containing a significant amount...... of alkali metal and/or alkali-earth compounds which process comprises using a catalyst combined of (i) a formed porous superacidic support, said superacidic support having an Hammett acidity stronger than Ho=-12, and (ii) a metal oxide catalytic component deposited on said superacidic support selected from...

  4. Novel synthesis of layered double hydroxides (LDHs) from zinc hydroxide (United States)

    Meng, Zilin; Zhang, Yihe; Zhang, Qian; Chen, Xue; Liu, Leipeng; Komarneni, Sridhar; Lv, Fengzhu


    The most common synthesis methods for layered double hydroxides (LDHs) are co-precipitation and reconstruction, which can have some limitations for application. Here, we report a novel synthesis method for LDHs. We use zinc hydroxide as the precursor to synthesize LDHs phase through a simple transformation process of zinc hydroxide phase. For this transformation process, aluminum can enter into zinc hydroxide and replace zinc quickly to transform it into LDH by creating positive charges in the zinc hydroxide solid phase. The mechanism of LDH formation was through Al3+ reaction first with zinc hydroxide followed by recrystallization of the original structure of zinc hydroxide. Thus, the new process of LDH formation involves a reaction of Al to substitute for Zn and recrystallization leading to LDH and the final pH influences the crystallization of LDHs by this process. In addition, Cr3+ was employed as a trivalent cation for LDH formation to react with zinc hydroxide, which also led to LDH structure.

  5. Microwave assisted alkali-catalyzed transesterification of Pongamia pinnata seed oil for biodiesel production. (United States)

    Kumar, Ritesh; Kumar, G Ravi; Chandrashekar, N


    In this study, microwave assisted transesterification of Pongamia pinnata seed oil was carried out for the production of biodiesel. The experiments were carried out using methanol and two alkali catalysts i.e., sodium hydroxide (NaOH) and potassium hydroxide (KOH). The experiments were carried out at 6:1 alcohol/oil molar ratio and 60°C reaction temperature. The effect of catalyst concentration and reaction time on the yield and quality of biodiesel was studied. The result of the study suggested that 0.5% sodium hydroxide and 1.0% potassium hydroxide catalyst concentration were optimum for biodiesel production from P. pinnata oil under microwave heating. There was a significant reduction in reaction time for microwave induced transesterification as compared to conventional heating.

  6. Assesment of Alkali Resistance of Basalt Used as Concrete Aggregates

    Directory of Open Access Journals (Sweden)

    al-Swaidani Aref M.


    Full Text Available The objective of this paper is to report a part of an ongoing research on the influence of using crushed basalt as aggregates on one of durability-related properties of concrete (i.e. alkali-silica reaction which is the most common form of Alkali-Aggregate Reaction. Alkali resistance has been assessed through several methods specified in the American Standards. Results of petrographic examination, chemical test (ASTM C289 and accelerated mortar bar test (ASTM C1260 have particularly been reported. In addition, the weight change and compressive strength of 28 days cured concrete containing basaltic aggregates were also reported after 90 days of exposure to 10% NaOH solution. Dolomite aggregate were used in the latter test for comparison. The experimental results revealed that basaltic rocks quarried from As-Swaida’a region were suitable for production of aggregates for concrete. According to the test results, the studied basalt aggregates can be classified as innocuous with regard to alkali-silica reaction. Further, the 10% sodium hydroxide attack did not affect the compressive strength of concrete.

  7. Microwave-based alkali pretreatment of switchgrass and coastal bermudagrass for bioethanol production. (United States)

    Keshwani, Deepak R; Cheng, Jay J


    Switchgrass and coastal bermudagrass are promising lignocellulosic feedstocks for bioethanol production. However, pretreatment of lignocelluloses is required to improve production of fermentable sugars from enzymatic hydrolysis. Microwave-based alkali pretreatment of switchgrass and coastal bermudagrass was investigated in this study. Pretreatments were carried out by immersing the biomass in dilute alkali reagents and exposing the slurry to microwave radiation at 250 W for residence times ranging from 5 to 20 min. Simons' stain method was used to quantify changes in biomass porosity as a result of the pretreatment. Pretreatments were evaluated based on yields of total reducing sugars, glucose, and xylose. An evaluation of different alkalis identified sodium hydroxide as the most effective alkali reagent for microwave-based pretreatment of switchgrass and coastal bermudagrass. 82% glucose and 63% xylose yields were achieved for switchgrass and 87% glucose and 59% xylose yields were achieved for coastal bermudagrass following enzymatic hydrolysis of biomass pretreated under optimal conditions. Dielectric properties for dilute sodium hydroxide solutions were measured and compared with solid losses, lignin reduction, and reducing sugar levels in hydrolyzates. Results indicate that dielectric loss tangent of alkali solutions is a potential indicator of the severity of microwave-based pretreatments.

  8. The calcium-alkali syndrome


    Arroyo, Mariangeli; Fenves, Andrew Z.; Emmett, Michael


    The milk-alkali syndrome was a common cause of hypercalcemia, metabolic alkalosis, and renal failure in the early 20th century. It was caused by the ingestion of large quantities of milk and absorbable alkali to treat peptic ulcer disease. The syndrome virtually vanished after introduction of histamine-2 blockers and proton pump inhibitors. More recently, a similar condition called the calcium-alkali syndrome has emerged as a common cause of hypercalcemia and alkalosis. It is usually caused b...

  9. Behaviour of gaseous alkali compounds in coal gasification; Kaasumaisten alkaliyhdisteiden kaeyttaeytyminen kivihiilien kaasutuksessa

    Energy Technology Data Exchange (ETDEWEB)

    Nykaenen, J. [Imatran Voima Oy, Vantaa (Finland)


    In this project the behaviour of alkali compounds emitting from CO{sub 2}/O{sub 2}- and airblown gasification are studied. This research project is closely connected to an EU-project coordinated by the Delft University of Technology (DUT). In that project alkali emissions from a 1.6 MW pilot plant will be measured. The results from those measurements will be compared with the calculations performed in this LIEKKI 2 project. The equilibrium calculations show that the major gaseous alkali compounds emitting from combustion and gasification are chlorides and hydroxides. This applies both to air- and CO{sub 2}/O{sub 2}-blown processes. In all the cases studied the concentration of gaseous alkali compounds is determined mainly by the amount of chlorides. The key parameters, with respect to alkali behaviour, are the temperature of the process and chlorine content of the coal. By cooling the gases down to 600 deg C prior to a ceramic filter the alkali concentration can be kept about at 100 ppbv. In combustion, the addition of calcium carbonate increases the amount of gaseous alkali compounds by decreasing the amount of alkali sulphates. In the case of gasification the importance of limestone is negligible. The difference between air- and CO{sub 2}/O{sub 2}-blown processes, in terms of gaseous alkali emissions, is small. This is because CO{sub 2} concentration of the gas does not have a strong impact on alkali chlorides. Furthermore, the effect of CO{sub 2}/O{sub 2}-ratio of the recirculation process is negligible. (orig.)

  10. Effect of high-energy radiation and alkali treatment on the properties of cellulose

    Energy Technology Data Exchange (ETDEWEB)

    Foeldvary, Cs.M. E-mail:; Takacs, E.; Wojnarovits, L


    The effect of the treatment with NaOH or tetramethyl ammonium hydroxide solutions on preirradiated cotton-cellulose was investigated. Both the radiation and the treatment with alkali solutions caused loss of weight in cellulose; however, there was a synergism, a high weight loss was observed during alkali treatment of preirradiated samples. The radiation caused scissions of the cellulose chains and during the treatment with aqueous alkaline solutions some smaller fragments dissolved, resulting in a strong absorbance of the solutions with maximum at around 268 nm. It was attributed to the absorbance of aldehyde/keto groups.

  11. Physical and Thermal Characterization of Alkali Treated Rice Husk Reinforced Polypropylene Composites

    Directory of Open Access Journals (Sweden)

    Ismat Zerin Luna


    Full Text Available Rice husk (RH reinforced polypropylene- (PP- based composites were prepared by compression molding. The RH was treated with sodium hydroxide solution (1 wt%; then composites were prepared using varying percentages of RH (5 to 20 wt%. The thermomechanical, spectroscopic, and morphological properties of the prepared composites (RH-PP were investigated. The scanning electron microscopic (SEM analysis showed better interfacial adhesion between alkali treated RH and the matrix PP. The Fourier Transform Infrared (FTIR spectra confirmed the chemical bonding.The results revealed that physical properties as well as thermal stability of the composites improved significantly with the addition of alkali treated RH in PP matrix.

  12. Highly dispersed iron species created on alkali-treated zeolite for ammonia SCR

    Institute of Scientific and Technical Information of China (English)

    Jing Ma; Duan Weng; Xiaodong Wu; Zhichun Si; Zhenwei Wu


    Alkaline treatment using sodium hydroxide was introduced to obtain a hierarchical pore structure in H-ZSM-5 zeolite. Fe-exchanged zeolite catalysts were prepared by impregnation on the original and alkali-treated zeolites, and were evaluated for NOx reduction by NH3, NO oxidation, and NH3 oxidation reactions. The highly dispersed iron species as active sites can be obtained by controlling the pore structure and particle size of zeolite. Therefore, the Fe/ZSM-5 catalyst treated mildly by sodium hydroxide before iron exchange, which contains amounts of highly dispersed Fe species, obtains over 80% NOx conversion at a wide temperature range of 250-500 1C.

  13. Alkali Aggregate Reaction in Alkali Slag Cement Mortars

    Institute of Scientific and Technical Information of China (English)


    By means of "Mortar Bar Method",the ratio of cement to aggregate was kept as a constant 1∶2.25,the water-cement ratio of the mixture was 0.40,and six prism specimens were prepared for each batch of mixing proportions with dimensions of 10×10×60mm3 at 38±2℃ and RH≥95%, the influences of content and particle size of active aggregate, sort and content of alkali component and type of slag on the expansion ratios of alkali-activated slag cement(ASC) mortars due to alkali aggregate reaction(AAR) were studied. According to atomic absorption spectrometry,the amount of free alkali was measured in ASC mortars at 90d.The results show above factors affect AAR remarkably,but no dangerous AAR will occur in ASC system when the amount of active aggregate is below 15% and the mass fraction of alkali is not more than 5% (Na2O).Alkali participated in reaction as an independent component, and some hydrates containing alkali cations were produced, free alkalis in ASC system can be reduced enormously.Moreover,slag is an effective inhibitor, the possibility of generating dangerous AAR in ASC system is much lower at same conditions than that in ordinary Portland cement system.

  14. Natural Alkali Shifts to the Methanol Business

    Institute of Scientific and Technical Information of China (English)


    @@ Inner Mongolia Yuanxing Natural Alkali Co., Ltd. (Natural Alkali SZ: 000683) established in 1997 is a large chemical enterprise with new energy as its leading business and natural gas chemicals and natural alkali chemicals as the supplement business.

  15. Scientific Opinion on the safety and efficacy of sodium hydroxide for dogs, cats and ornamental fish

    Directory of Open Access Journals (Sweden)

    EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP


    Full Text Available

    The additive consists, by specification, of a minimum of 98.0 % sodium hydroxide or alkali in the solid form, the content of solutions scaled accordingly, based on the stated or labelled concentration. No data have been provided that would support the specification of the solid form, only a 50.0 % w/w solution of sodium hydroxide in water, which is the final product of the production process described in the dossier. Sodium hydroxide is considered safe for the target animals, provided that the resulting total sodium concentration in feed does not compromise the overall electrolyte balance. Sodium hydroxide in solid form and in aqueous solution at concentrations > 8.0 % is corrosive. At lower concentrations it is irritant to skin and eyes (0.5 % and 0.2 %, respectively and the respiratory tract (0.5 %. Exposure via inhalation is likely to be minimal. Sodium hydroxide is not considered to be a skin sensitiser. As sodium hydroxide is used in food as an acidity regulator, and its function in feed is essentially the same as that in food, no further demonstration of efficacy is necessary.

  16. An empirical model to estimate density of sodium hydroxide solution: An activator of geopolymer concretes (United States)

    Rajamane, N. P.; Nataraja, M. C.; Jeyalakshmi, R.; Nithiyanantham, S.


    Geopolymer concrete is zero-Portland cement concrete containing alumino-silicate based inorganic polymer as binder. The polymer is obtained by chemical activation of alumina and silica bearing materials, blast furnace slag by highly alkaline solutions such as hydroxide and silicates of alkali metals. Sodium hydroxide solutions of different concentrations are commonly used in making GPC mixes. Often, it is seen that sodium hydroxide solution of very high concentration is diluted with water to obtain SHS of desired concentration. While doing so it was observed that the solute particles of NaOH in SHS tend to occupy lower volumes as the degree of dilution increases. This aspect is discussed in this paper. The observed phenomenon needs to be understood while formulating the GPC mixes since this influences considerably the relationship between concentration and density of SHS. This paper suggests an empirical formula to relate density of SHS directly to concentration expressed by w/w.

  17. Process optimization of reaction of acid leaching residue of asbestos tailing and sodium hydroxide aqueous solution

    Institute of Scientific and Technical Information of China (English)

    DU GaoXiang; ZHENG ShuiLin; DING Hao


    Silica is the major component of the acid leaching residue of asbestos tailing. The waterglass solution can be prepared by the reaction of the residue with sodium hydroxide aqueous solution. Compared to the high temperature reaction method, this process is environmental friendly and low cost. In this paper, the reaction process of the residue and the sodium hydroxide aqueous solution is optimized. The op-timum reaction process parameters are as follows: the usage of sodium hydroxide is 26.4 g/100 g acid leaching residue, the reaction temperature is 90℃, the reaction time is 1 h, and the ratio of the liq-uid/solid is 2.0. The significance sequence of the process parameters to the alkali leaching reaction effect is the usage of sodium hydroxide > the ratio of the liquid/solid > the reaction time > the reaction temperature. The significance sequence to the leaching ratio of SiO2 is the ratio of the liquid/solid > the usage of sodium hydroxide > the reaction time > the reaction temperature. The significance sequence to the modulus of the sodium silicate is the ratio of the liquid/solid > the usage of sodium hydroxide > the reaction time > the reaction temperature. Under the optimum conditions, the leaching ratio of the SiO2 is 77.5%, and the modulus of the sodium silicate is 3.15. The XRD analysis result indicates that the major components of the alkali leaching residue are serpentine, talc, quartz and some albite.

  18. Alkali metal and alkali earth metal gadolinium halide scintillators

    Energy Technology Data Exchange (ETDEWEB)

    Bourret-Courchesne, Edith; Derenzo, Stephen E.; Parms, Shameka; Porter-Chapman, Yetta D.; Wiggins, Latoria K.


    The present invention provides for a composition comprising an inorganic scintillator comprising a gadolinium halide, optionally cerium-doped, having the formula A.sub.nGdX.sub.m:Ce; wherein A is nothing, an alkali metal, such as Li or Na, or an alkali earth metal, such as Ba; X is F, Br, Cl, or I; n is an integer from 1 to 2; m is an integer from 4 to 7; and the molar percent of cerium is 0% to 100%. The gadolinium halides or alkali earth metal gadolinium halides are scintillators and produce a bright luminescence upon irradiation by a suitable radiation.

  19. Synergistic capture mechanisms for alkali and sulfur species from combustion. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Peterson, T.W.; Shadman, F.; Wendt, J.O.L.; Mwabe, P.O.


    Experimental work was carried out on a 17 kW, 600 cm long, gas laboratory combustor, to investigate the post flame reactive capture of alkali species by kaolinite. Emphasis was on alkali/sorbent interactions occurring in flue gas at temperatures above the alkali dewpoint and on the formation of water insoluble reaction products. Time-temperature studies were carried out by injecting kaolinite at different axial points along the combustor. The effect of chlorine and sulfur on alkali capture was investigated by doping the flame with SO{sub 2} and Cl{sub 2} gases to simulate coal flame environments. Particle time and temperature history was kept as close as possible to that which would ordinarily be found in a practical boiler. Experiments designed to extract apparent initial reaction rates were carried using a narrow range, 1-2 {mu}m modal size sorbent, while, a coarse, multi size sorbent was used to investigate the governing transport mechanisms. The capture reaction has been proposed to be between alkali hydroxide and activated kaolinite, and remains so in the presence of sulfur and chlorine. The presence of sulfur reduces sodium capture by under 10% at 1300{degree}C. Larger reductions at lower temperatures are attributed to the elevated dewpoint of sodium ({approximately}850{degree}C) with subsequent reduction in sorbent residence time in the alkali gas phase domain. Chlorine reduces sodium capture by 30% across the temperature range covered by the present experiments. This result has been linked to thermodynamic equilibria between sodium hydroxide, sodium chloride and water.

  20. Upgrading platform using alkali metals

    Energy Technology Data Exchange (ETDEWEB)

    Gordon, John Howard


    A method for removing sulfur, nitrogen or metals from an oil feedstock. The method involves reacting the oil feedstock with an alkali metal and a radical capping substance. The alkali metal reacts with the metal, sulfur or nitrogen content to form one or more inorganic products and the radical capping substance reacts with the carbon and hydrogen content to form a hydrocarbon phase. The inorganic products may then be separated out from the hydrocarbon phase.

  1. Upgrading platform using alkali metals

    Energy Technology Data Exchange (ETDEWEB)

    Gordon, John Howard


    A process for removing sulfur, nitrogen or metals from an oil feedstock (such as heavy oil, bitumen, shale oil, etc.) The method involves reacting the oil feedstock with an alkali metal and a radical capping substance. The alkali metal reacts with the metal, sulfur or nitrogen content to form one or more inorganic products and the radical capping substance reacts with the carbon and hydrogen content to form a hydrocarbon phase. The inorganic products may then be separated out from the hydrocarbon phase.

  2. Studies on interfacial behavior and wettability change phenomena by ionic and nonionic surfactants in presence of alkalis and salt for enhanced oil recovery (United States)

    Kumar, Sunil; Mandal, Ajay


    Surfactant flooding is one of the most promising method of enhanced oil recovery (EOR) used after the conventional water flooding. The addition of alkali improves the performance of surfactant flooding due to synergistic effect between alkali and surfactant on reduction of interfacial tension (IFT), wettability alteration and emulsification. In the present study the interfacial tension, contact angle, emulsification and emulsion properties of cetyltrimethylammonium bromide (CTAB), sodium dodecyl sulfate (SDS) and polysorbate 80 (Tween 80) surfactants against crude oil have been investigated in presence of sodium chloride (NaCl) and alkalis viz. sodium hydroxide (NaOH), sodium carbonate (Na2CO3), ammonium hydroxide (NH4OH), sodium metaborate (SMB) and diethanolamine (DEA). All three surfactants significantly reduce the IFT values, which are further reduced to ultra-low value (∼10-4 mN/m) by addition of alkalis and salt. It has been found experimentally that alkali-surfactant systems change the wettability of an intermediate-wet quartz rock to water-wet. Emulsification of crude oil by surfactant and alkali has also been investigated in terms of the phase volume and stability of emulsion. A comparative FTIR analysis of crude oil and different emulsions were performed to investigate the interactions between crude oil and displacing water in presence of surfactant and alkali.


    Directory of Open Access Journals (Sweden)

    Sheldeshov N. V.


    Full Text Available The results of study of bipolar membrane – analogue of MB-2, modified with chemically introduced chromium (III, iron (III and nickel (II hydroxides by the method of frequency spectrum of electrochemical impedance, by infrared spectroscopy and scanning electron microscopy in combination with X-ray spectrum analysis are presented. It is shown, that sequential treatment of cation-exchanger, contained in cationexchange membrane, with metal salt solution and alkali solution does not result in formation of complex compounds of these metals with ionic groups of ion exchanger. It was found that in these conditions the presence of heavy metals in the phase of cationexchanger confirmed by X-ray analysis, however, crystals of hydroxides of heavy metals are not detected in the size range of 1000 nm to 20 nm. These heavy metal compounds are thermally unstable and their catalytic activity in the reaction of dissociation of water molecules decreases with increasing temperature during heat treatment. The introduction of low-soluble hydroxides of d-metals (chromium (III, iron (III, nickel(II by chemical method can significantly improve the electrochemical characteristics of a bipolar membrane. The most effective catalysts in water dissociation reaction are the hydroxides of chromium (III and iron (III and, as a consequence, membranes with these hydroxides have a lower value of overpotential compared with original membrane at the same current density

  4. 21 CFR 184.1428 - Magnesium hydroxide. (United States)


    ... hydration of reactive grades of magnesium oxide. (b) The ingredient meets the specifications of the Food... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Magnesium hydroxide. 184.1428 Section 184.1428 Food... Specific Substances Affirmed as GRAS § 184.1428 Magnesium hydroxide. (a) Magnesium hydroxide (Mg(OH)2,...

  5. Contribution to the knowledge of nickel hydroxide electrodes. 5. Analysis and electrochemical behavior of cadmium nickel hydroxides (United States)

    Bode, H.; Dennstedt, W.


    Electrochemical experiments performed at sintered and bulk electrodes show that beta nickel hydroxide contains an electrochemically inactive proportion of cadmium hydroxide of up to 10%. The electrochemically ineffective cadmium hydroxide is homogeneously dissolved in beta nickel hydroxide.

  6. Analysis of barium hydroxide and calcium hydroxide slurry carbonation reactors

    Energy Technology Data Exchange (ETDEWEB)

    Patch, K.D.; Hart, R.P.; Schumacher, W.A.


    The removal of CO/sub 2/ from air was investigated by using a continuous-agitated-slurry carbonation reactor containing either barium hydroxide (Ba(OH)/sub 2/) or calcium hydroxide (Ca(OH)/sub 2/). Such a process would be applied to scrub /sup 14/CO/sub 2/ from stack gases at nuclear-fuel reprocessing plants. Decontamination factors were characterized for reactor conditions which could alter hydrodynamic behavior. An attempt was made to characterize reactor performance with models assuming both plug flow and various degrees of backmixing in the gas phase. The Ba(OH)/sub 2/ slurry enabled increased conversion, but apparently the process was controlled under some conditions by phenomena differing from those observed for carbonation by Ca(OH)/sub 2/. Overall reaction mechanisms are postulated.

  7. Ions in water: the microscopic structure of concentrated hydroxide solutions. (United States)

    Imberti, S; Botti, A; Bruni, F; Cappa, G; Ricci, M A; Soper, A K


    Neutron-diffraction data on aqueous solutions of hydroxides, at solute concentrations ranging from 1 solute per 12 water molecules to 1 solute per 3 water molecules, are analyzed by means of a Monte Carlo simulation (empirical potential structure refinement), in order to determine the hydration shell of the OH- in the presence of the smaller alkali metal ions. It is demonstrated that the symmetry argument between H+ and OH- cannot be used, at least in the liquid phase at such high concentrations, for determining the hydroxide hydration shell. Water molecules in the hydration shell of K+ orient their dipole moment at about 45 degrees from the K+-water oxygen director, instead of radially as in the case of the Li+ and Na+ hydration shells. The K+-water oxygen radial distribution function shows a shallower first minimum compared to the other cation-water oxygen functions. The influence of the solutes on the water-water radial distribution functions is shown to have an effect on the water structure equivalent to an increase in the pressure of the water, depending on both ion concentration and ionic radius. The changes of the water structure in the presence of charged solutes and the differences among the hydration shells of the different cations are used to present a qualitative explanation of the observed cation mobility.

  8. The Durability and Performance of Short Fibers for a Newly Developed Alkali-Activated Binder

    Directory of Open Access Journals (Sweden)

    Henrik Funke


    Full Text Available This study reports the development of a fiber-reinforced alkali-activated binder (FRAAB with an emphasis on the performance and the durability of the fibers in the alkaline alkali-activated binder (AAB-matrix. For the development of the matrix, the reactive components granulated slag and coal fly ash were used, which were alkali-activated with a mixture of sodium hydroxide (2–10 mol/L and an aqueous sodium silicate solution (SiO2/Na2O molar ratio: 2.1 at ambient temperature. For the reinforcement of the matrix integral fibers of alkali-resistant glass (AR-glass, E-glass, basalt, and carbon with a fiber volume content of 0.5% were used. By the integration of these short fibers, the three-point bending tensile strength of the AAB increased strikingly from 4.6 MPa (no fibers up to 5.7 MPa (carbon after one day. As a result of the investigations of the alkali resistance, the AR-glass and the carbon fibers showed the highest durability of all fibers in the FRAAB-matrix. In contrast to that, the weight loss of E-glass and basalt fibers was significant under the alkaline condition. According to these results, only the AR-glass and the carbon fibers reveal sufficient durability in the alkaline AAB-matrix.

  9. Supermolecular layered dou- ble hydroxides

    Institute of Scientific and Technical Information of China (English)


    Research progresses in the layered double hydroxides ·mH2O intercalated with metal coordinate ions or oxometalates in the last ten years are reviewed. These layered double hydroxides are mainly intercalated with polyoxometalate (POM) ions, a LiAl-LDH photochemical assembly containing TiO2 and CH3(CH2)12COO- anions, together with Zn(TPPC) (porphy-rin derivate) and macrocyclic ligand-containing porphyrin derivate anions. Emphasis is put on the synthesis methods for intercalation of the anions into the interlayer regions, the characterization techniques and structures for the layered compounds and the newest research progress in the fields such as catalysis. The review also forecasts the prospects of the field.

  10. Process for recovering alkali metals and sulfur from alkali metal sulfides and polysulfides

    Energy Technology Data Exchange (ETDEWEB)

    Gordon, John Howard; Alvare, Javier


    Alkali metals and sulfur may be recovered from alkali monosulfide and polysulfides in an electrolytic process that utilizes an electrolytic cell having an alkali ion conductive membrane. An anolyte solution includes an alkali monosulfide, an alkali polysulfide, or a mixture thereof and a solvent that dissolves elemental sulfur. A catholyte includes molten alkali metal. Applying an electric current oxidizes sulfide and polysulfide in the anolyte compartment, causes alkali metal ions to pass through the alkali ion conductive membrane to the catholyte compartment, and reduces the alkali metal ions in the catholyte compartment. Liquid sulfur separates from the anolyte solution and may be recovered. The electrolytic cell is operated at a temperature where the formed alkali metal and sulfur are molten.

  11. A negative ion source for alkali ions

    NARCIS (Netherlands)

    Vermeer, A.; Zwol, N.A. van


    An ion source is described which delivers negative alkali ions. With this source, which consists of a duoplasmatron and a charge exchange canal with alkali vapour, negative Li, Na and K ions are produced. The oven in which alkali metals are evaporated can reach temperatures up to 575°C.

  12. Alkali binding in hydrated Portland cement paste

    NARCIS (Netherlands)

    Chen, W.; Brouwers, H.J.H.


    The alkali-binding capacity of C–S–H in hydrated Portland cement pastes is addressed in this study. The amount of bound alkalis in C–S–H is computed based on the alkali partition theories firstly proposed by Taylor (1987) and later further developed by Brouwers and Van Eijk (2003). Experimental data

  13. Use of slag/sugar cane bagasse ash (SCBA) blends in the production of alkali-activated materials


    María V. Borrachero; Jordi Payá; José Monzó; Lourdes Soriano; Mauro M. Tashima; José L.P. Melges; Jorge L. Akasaki; Vinícius N. Castaldelli


    Blast furnace slag (BFS)/sugar cane bagasse ash (SCBA) blends were assessed for the production of alkali-activated pastes and mortars. SCBA was collected from a lagoon in which wastes from a sugar cane industry were poured. After previous dry and grinding processes, SCBA was chemically characterized: it had a large percentage of organic matter (ca. 25%). Solutions of sodium hydroxide and sodium silicate were used as activating reagents. Different BFS/SCBA mixtures were studied, replacing part...

  14. Study of Zinc Leaching of EAF Flue Dust Using Sodium Hydroxide

    Directory of Open Access Journals (Sweden)

    Ahsan Abdul Ghani


    Full Text Available During the production of steel from Electric Arc Furnace (EAF, large amount of by-product called EAF flue dust is generated. The major proportion of flue dust is comprised of Zn (41.5 % wt.. Different phases identified by XRD analysis are zincite, franklinite and magnetite with zincite being dominant. In this study, we have performed flue dust treatment using sodium hydroxide as leaching medium. Different concentrations of alkali were used to optimize maximum recovery of Zn. XRF and Wet Chemical method were used to characterize the dust samples both before and after leaching. The optimum alkali concentration for selective leaching of zinc was found to be 4 M with a zinc recovery of 90 %.

  15. Alkali-metalated forms of thiacalix[4]arenes. (United States)

    Zeller, Jürgen; Radius, Udo


    The alkali metal salts [TCALi4] (1), [TCANa4] (2), and [TCALK4] (3) of fully deprotonated p-tert-butyltetrathiacalix[4]arene (H(4)TCA) are readily available from the reactions of thiacalix[4]arene and n-BuLi, NaH, or KH as deprotonating reagents. Crystals of the sodium salts 2 and the potassium salt 3 suitable for X-ray diffraction were obtained in the form of the pyridine solvates [(TCA)2Na8.8py] (2.8py) and [(TCA)2K(8).8py] (3.8py). These molecules are dimers in the solid state but are structurally not related. In addition, the reaction of H(4)TCA and lithium hydroxide afforded the structurally characterized complex [(TCA)Li5(OH).4THF] (4). The molecular structure of 4 as well as the structures of 2.8py and 3.8py reveal a close relationship to the corresponding alkali metal salts of the calix[4]arenes.

  16. Sequential acid-/alkali-pretreatment of empty palm fruit bunch fiber. (United States)

    Kim, Seonghun; Park, Jang Min; Seo, Jeong-Woo; Kim, Chul Ho


    Pretreatment processes are key technologies for generating fermentable sugars based on lignocellulosic biomass. In this study, we developed a novel method for empty palm fruit bunch fiber (EPFBF) using sequential pretreatment with dilute acid and then alkali. Dilute sulfuric acid was used in the first step, which removed 90% of the hemicellulose and 32% of the lignin, but left most of the cellulose under the optimum pretreatment condition. Sodium hydroxide was then applied in the second step, which extracted lignin effectively with a 70% delignification yield, partially disrupting the ordered fibrils of the EPFBF and thus enhancing the enzyme digestibility of the cellulose. The sequentially pretreated biomass consisted of 82% cellulose, less than 1% hemicellulose, and 30% lignin content afterward. The pretreated biomasses morphologically revealed rough, porous, and irregularly ordered surfaces for enhancing enzyme digestibility. These results indicate that the sequentially acid/alkali-pretreated EPFBF could be broadly useful as a novel biomass.

  17. Positron-alkali atom scattering (United States)

    Mceachran, R. P.; Horbatsch, M.; Stauffer, A. D.; Ward, S. J.


    Positron-alkali atom scattering was recently investigated both theoretically and experimentally in the energy range from a few eV up to 100 eV. On the theoretical side calculations of the integrated elastic and excitation cross sections as well as total cross sections for Li, Na and K were based upon either the close-coupling method or the modified Glauber approximation. These theoretical results are in good agreement with experimental measurements of the total cross section for both Na and K. Resonance structures were also found in the L = 0, 1 and 2 partial waves for positron scattering from the alkalis. The structure of these resonances appears to be quite complex and, as expected, they occur in conjunction with the atomic excitation thresholds. Currently both theoretical and experimental work is in progress on positron-Rb scattering in the same energy range.

  18. Pharmacokinetic Profile of Oral Magnesium Hydroxide

    DEFF Research Database (Denmark)

    Dolberg, Mette Konow Bøgebjerg; Nielsen, Lars Peter; Dahl, Ronald


    Despite the presumption of a beneficial effect of magnesium (Mg) supplementation on various diseases, little is known concerning the pharmacokinetics of Mg hydroxide. This study was designed to provide a pharmacokinetic profile of Mg hydroxide after a single oral dose. Ten healthy male adults...

  19. Alkali-Resistant Quasi-Solid-State Electrolyte for Stretchable Supercapacitors. (United States)

    Tang, Qianqiu; Wang, Wenqiang; Wang, Gengchao


    Research on stretchable energy-storage devices has been motivated by elastic electronics, and considerable research efforts have been devoted to the development of stretchable electrodes. However, stretchable electrolytes, another critical component in stretchable devices, have earned quite little attention, especially the alkali-resistant ones. Here, we reported a novel stretchable alkali-resistant electrolyte made of a polyolefin elastomer porous membrane supported potassium hydroxide-potassium polyacrylate (POE@KOH-PAAK). The as-prepared electrolyte shows a negligible plastic deformation even after 1000 stretching cycles at a strain of 150% as well as a high conductivity of 0.14 S cm(-1). It also exhibits excellent alkali resistance, which shows no obvious degradation of the mechanical performance after immersion in 2 M KOH for up to 2 weeks. To demonstrate its good properties, a high-performance stretchable supercapacitor is assembled using a carbon-nanotube-film-supported NiCo2O4 (CNT@NiCo2O4) as the cathode and Fe2O3 (CNT@Fe2O3) as the anode, proving great application promise of the stretchable alkali-resistant electrolyte in stretchable energy-storage devices.

  20. Extraction of Alkali Ions Investigated by Conductometric and pH Measurements

    Directory of Open Access Journals (Sweden)

    L. Kalvoda


    Full Text Available Extraction of alkali ions from aqueous solutions of chlorides and hydroxides into a lipophilic liquid membrane composed of tetraethyl p-tert-butylcalix[4]arene tetraacetate (TBT solution in hexane was investigated by means of measurements of changes in the electrolytic conductivity and pH-value of the aqueous solution. Hydrolysis of the TBT ionophore resulting in the release of the ethyl groups was proposed as the main reaction process, leading to disturbance of the known preference of TBT for sodium ions. 

  1. Alkali-silica reaction resistant concrete using pumice blended cement (United States)

    Ramasamy, Uma

    Durability of structures is a major challenge for the building industry. One of the many types of concrete deterioration that can affect durability is alkali-silica reaction (ASR). ASR has been found in most types of concrete structures, including dams, bridges, pavements, and other structures that are 20 to 50 years old. The degradation mechanism of ASR produces a gel that significantly expands in the presence of water as supplied from the surrounding environment. This expansion gel product can create high stresses and cracking of the concrete, which can lead to other forms of degradation and expensive structural replacement costs. The four essential factors that produce an expansive ASR gel in concrete are the presence of alkalis, siliceous aggregate, moisture, and free calcium hydroxide (CH). If concrete is starved of any one of these essential components, the expansion can be prevented. Reducing CH through the use of a supplementary cementitious material (SCM) such as natural pozzolan pumice is the focus of this research. By using a pozzolan, the amount of CH is reduced with time based on the effectiveness of the pozzolan. Many pozzolans exist, but one such naturally occurring pozzolanic material is pumice. This research focuses on determining the effect of a finely ground pumice as a SCM in terms of its resistance to ASR expansion, as well as improving resistance to other potential concrete durability mechanisms. In spite of having high alkali contents in the pumice, mixtures containing the SCM pumice more effectively mitigated the ASR expansion reaction than other degradation mechanisms. Depending on the reactivity of the aggregates and fineness of the pumice, 10-15% replacement of cement with the pumice was found to reduce the ASR expansion to the acceptable limits. The amount of CH remaining in the concrete was compared to the ASR expansion in order to improve understanding of the role of CH in the ASR reaction. Thermo-gravimetric analysis (TGA) and X

  2. Performance characterization of rigid polyurethane foam with refined alkali lignin and modified alkali lignin

    Institute of Scientific and Technical Information of China (English)

    LIU Zhi-ming; YU Fei; FANG Gui-zhen; YANG Hui-jun


    The two kinds of rigid polyurethane (PU) foams were prepared with respectively adding the refined alkali lignin and alkali lignin modified by 3-chloro-1,2-epoxypropane to be instead of 15% of the polyether glycol in weight. The indexes of mechanical performance, apparent density, thermal stability and aging resistance were separately tested for the prepared PU foams. The results show that the mechanical property, thermal insulation and thermal stability for PU foam with modified alkali lignin are excellent among two kinds of PU foams and control samples. The additions of the refined alkali lignin and modified alkali lignin to PU foam have little effect on the natural aging or heat aging resistance except for decreasing hot alkali resistance apparently. Additionally, the thermal conductivity of modified alkali lignin PU foam is lowest among two kinds of PU foams and control samples. The alkali lignin PU foam modified by 3-chloro-1,2-epoxypropane could be applied in the heat preservation field.

  3. Properties of oxide-hydroxide sintered ceramics (United States)

    Levkov, R. V.; Kulkov, S. N.


    In this paper the study of porous ceramics obtained from aluminum hydroxide with gibbsite modification is presented. It was shown that aluminum hydroxide may be used for pore formation and pore volume in the sintered ceramics can be controlled by varying the aluminum hydroxide concentration and sintering temperature. It was shown that compressive strength of alumina ceramics increases by 40 times with decreasing the pore volume from 65 to 15%. Based on these results one can conclude that the obtained structure is very close to inorganic bone matrix and can be used as promising material for bone implants production.

  4. Thermodynamics of Volatile Silicon Hydroxides Studied (United States)

    Copland, Evan H.; Opila, Elizabeth J.; Jacobson, Nathan S.


    Silicon-based ceramics are promising candidate structural materials for heat engines. The long-term stability of these materials to environmental degradation is dependent on the formation and retention of a protective SiO2 layer. It is well known that SiO2 forms stable volatile hydroxides in the presence of water vapor at elevated temperatures. Combustion conditions, which characteristically are at high velocities, contain significant water vapor pressures, and high temperatures tend to promote continuous formation of these hydroxides with resulting material degradation. For the degradation of silicon-based ceramics to be predicted, accurate thermodynamic data on the formation of silicon hydroxides are needed.

  5. Role of sodium hydroxide in the production of hydrogen gas from the hydrothermal gasification of biomass

    Energy Technology Data Exchange (ETDEWEB)

    Onwudili, Jude A.; Williams, Paul T. [Energy and Resources Research Institute, University of Leeds, Leeds, LS2 9JT (United Kingdom)


    The role of sodium hydroxide as a promoter of hydrogen gas production during the hydrothermal gasification of glucose and other biomass samples has been investigated. Experiments were carried out in a batch reactor with glucose and also in the presence of the alkali from 200 C, 2 MPa to 450 C, 34 MPa at constant water loading. Without sodium hydroxide, glucose decomposed to produce mainly carbon dioxide, water, char and tar. Furfural, its derivatives and reaction products dominated the ethyl acetate extract of the water (organic fraction) at lower reaction conditions. This indicated that the dehydration of glucose to yield these products was unfavourable to hydrogen gas production. In the presence of sodium hydroxide however, glucose initially decomposed to form mostly alkylated and hydroxylated carbonyl compounds, whose further decomposition yielded hydrogen gas. It was observed that at 350 C, 21.5 MPa, half of the optimum hydrogen gas yield had formed and at 450 C, 34 MPa, more than 80 volume percent of the gaseous effluent was hydrogen gas, while the balance was hydrocarbon gases, mostly methane ({>=}10 volume percent). Other biomass samples were also comparably reacted at the optimum conditions observed for glucose. The rate of hydrogen production for the biomass samples was in the following order; glucose > cellulose, starch, rice straw > potato > rice husk. (author)

  6. Studies on MgNi-Based Metal Hydride Electrode with Aqueous Electrolytes Composed of Various Hydroxides

    Directory of Open Access Journals (Sweden)

    Jean Nei


    Full Text Available Compositions of MgNi-based amorphous-monocrystalline thin films produced by radio frequency (RF sputtering with a varying composition target have been optimized. The composition Mg52Ni39Co3Mn6 is identified to possess the highest initial discharge capacity of 640 mAh·g−1 with a 50 mA·g−1 discharge current density. Reproduction in bulk form of Mg52Ni39Co3Mn6 alloy composition was prepared through a combination of melt spinning (MS and mechanical alloying (MA, shows a sponge-like microstructure with >95% amorphous content, and is chosen as the metal hydride (MH alloy for a sequence of electrolyte experiments with various hydroxides including LiOH, NaOH, KOH, RbOH, CsOH, and (C2H54N(OH. The electrolyte conductivity is found to be closely related to cation size in the hydroxide compound used as 1 M additive to the 4 M KOH aqueous solution. The degradation performance of Mg52Ni39Co3Mn6 alloy through cycling demonstrates a strong correlation with the redox potential of the cation in the alkali hydroxide compound used as 1 M additive to the 5 M KOH aqueous solution. NaOH, CsOH, and (C2H54N(OH additions are found to achieve a good balance between corrosion and conductivity performances.

  7. Thermodynamic study of alkali metals release in pressurised fluidised-bed combustion and gasification of peat

    Energy Technology Data Exchange (ETDEWEB)

    Mojtahedi, W.; Backman, R.; Korhonen, M.


    A combined-cycle power generation system incorporating pressurised fluidised-bed combustion (PFBC) or gasification is considered a promising approach for electricity generation using solid fuels such as peat. In these systems, the high-pressure hot flue gas is expanded in a gas turbine. Peat contains sodium and potassium which are released in combustion and gasification. These are corrosive elements that can cause severe damage to the turbine blades if not suppressed. Multicomponent, multiphase equilibrium calculations were carried out for atmospheric and pressurised fluidised-bed operating conditions to determine the relative distribution of the two metals (Na and K) in the gas and condensed phases. Dependence of the alkali volatilisation on the operating temperature, pressure, the chlorine-content and the total alkali-content of the feedstock was studied. The results show that the alkali release in the vapour-phase could be much higher than acceptable to a gas turbine, particularly under gasification conditions. Hence the necessity to remove the volatilised alkali-metal compounds is more acute in gasification than in combustion. Both sodium and potassium are present as chlorides and to a lesser extent as hydroxides in the gas phase in both modes of operation (i.e. combustion and gasification). However, whereas under combustion conditions both metals seem to condense as sulphates (Na/sub 2/SO4 and K/sub 2/SO4), in gasification, chlorides and carbonates dominate in the condensed phase. The alkali-metals volatilisation shows strong dependence on the operating pressure of the system as well as on the chlorine-content of the feedstock. It decreases markedly with the former but increases sharply with the latter.

  8. Nickel hydroxide precipitation from aqueous sulfate media (United States)

    Sist, Cinziana; Demopoulos, George P.


    Hydrometallurgical processing of laterite ores constitutes a major industrial and R&D activity in extractive metallurgy. In some of the process flowsheets, nickel hydroxide precipitation is incorporated. For these operations, the optimization of nickel hydroxide precipitation is important to assure efficiency and product quality. The main objective of this investigation was to study and improve the precipitation characteristics of Ni(OH)2 in a sulfate system using supersaturation controlled precipitation.

  9. Effect of Alkali on Daqing Crude Oil/Water Interfacial Properties

    Institute of Scientific and Technical Information of China (English)

    Guo Jixiang; Li Mingyuan; Lin Meiqin; Wu Zhaoliang


    Alkaline-surfactant-polymer (ASP) flooding using sodium hydroxide as the alkali component to enhance oil recovery in Daqing Oilfield,northeast China has been successful,but there are new problems in the treatment of produced crude. The alkali added forms stable water-in-crude oil emulsion,hence de-emulsification process is necessary to separate oil and water. The problems in enhanced oil recovery with ASP flooding were investigated in laboratory by using fractions of Daqing crude oil. The oil was separated into aliphatics,aromatics,resin and asphaltene fractions. These fractions were then mixed with an additive-free jet fuel to form model oils. The interfacial properties,such as interfacial tension and interfacial pressure of the systems were also measured,which together with the molecular parameters of the fractions were all used to investigate the problems in the enhanced oil recovery. In our work,it was found that sodium hydroxide solution reacts with the acidic hydrogen in the fractions of crude oil and forms soap-like interfacially active components,which accumulate at the crude oil-water interface.

  10. Alkali Treatment of Acidic Solution from Hanford K Basin Sludge Dissolution

    Energy Technology Data Exchange (ETDEWEB)

    AA Bessonov; AB Yusov; AM Fedoseev; AV Gelis; AY Garnov; CH Delegard; GM Plavnik; LN Astafurova; MS Grigoriev; NA Budantseva; NN Krot; SI Nikitenko; TP Puraeva; VP Perminov; VP Shilov


    Nitric acid solutions will be created from the dissolution of Hanford K Basin sludge. These acidic dissolver solutions must be made alkaline by treatment with NaOH solution before they are disposed to ~ the Tank Waste Remediation System on the Hanford Site. During the alkali treatments, sodium diuranate, hydroxides of iron and aluminum, and radioelements (uranium, plutonium, and americium) will precipitate from the dissolver solution. Laboratory tests, discussed here, were pefiormed to provide information on these precipitates and their precipitation behavior that is important in designing the engineering flowsheet for the treatment process. Specifically, experiments were conducted to determine the optimum precipitation conditions; the completeness of uranium, plutonium, and americium precipitation; the rate of sedimentation; and the physico-chemical characteristics of the solids formed by alkali treatment of simulated acidic dissolver solutions. These experiments also determined the redistribution of uranium, plutonium, and americium flom the sodium di~ate and iron and al&inurn hydroxide precipitates upon contact with carbonate- and EDTA-bearing simulated waste solutions. Note: EDTA is the tetrasodium salt of ethylenediaminetetraacetate.


    Directory of Open Access Journals (Sweden)

    Heli Cheng


    Full Text Available A biorefinery using the process of hemicellulose pre-extraction and subsequent pulping provides a promising way for the utilization of straw biomass and resolution of problems related to silicon. In this work, hemicellulose was extracted from depithed corn stover with sodium hydroxide solution before soda-AQ pulping. Components of the extracts were quantified by ion chromatography. The parameters (alkali concentration and temperature affecting hemicellulose pre-extraction were optimized. The main constituent of hemicellulose in corn stover was xylan, which accounted for 18.1% of the depithed raw material. More than 90% of the xylan can be extracted under the optimal conditions: NaOH concentration of 10%, temperature of 75ºC, and time of 2h. Solid fractions after extraction were subjected to soda-AQ pulping. In comparison with control pulp obtained without extraction, it was found that alkali pre-extraction could improve the brightness and decrease kappa number of the subsequent pulp, causing a slight loss of yield, viscosity, density, and burst strength, but an obvious improvement of tear strength. Moreover, the silicon content was decreased by 79.8% when the extraction conditions were set at 75 ºC with alkali concentration of 8%, suggesting that pre-extraction of hemicellulose is a potential way to solve silicon problems associated with alkaline pulping of stover.

  12. Strength and durability performance of alkali-activated rice husk ash geopolymer mortar. (United States)

    Kim, Yun Yong; Lee, Byung-Jae; Saraswathy, Velu; Kwon, Seung-Jun


    This paper describes the experimental investigation carried out to develop the geopolymer concrete based on alkali-activated rice husk ash (RHA) by sodium hydroxide with sodium silicate. Effect on method of curing and concentration of NaOH on compressive strength as well as the optimum mix proportion of geopolymer mortar was investigated. It is possible to achieve compressive strengths of 31 N/mm(2) and 45 N/mm(2), respectively for the 10 M alkali-activated geopolymer mortar after 7 and 28 days of casting when cured for 24 hours at 60°C. Results indicated that the increase in curing period and concentration of alkali activator increased the compressive strength. Durability studies were carried out in acid and sulfate media such as H2SO4, HCl, Na2SO4, and MgSO4 environments and found that geopolymer concrete showed very less weight loss when compared to steam-cured mortar specimens. In addition, fluorescent optical microscopy and X-ray diffraction (XRD) studies have shown the formation of new peaks and enhanced the polymerization reaction which is responsible for strength development and hence RHA has great potential as a substitute for ordinary Portland cement concrete.

  13. Nanosized alkali-metal-doped ethoxotitanate clusters. (United States)

    Chen, Yang; Trzop, Elzbieta; Makal, Anna; Sokolow, Jesse D; Coppens, Philip


    The synthesis and crystallographic characterization of alkali-metal-doped ethoxotitanate clusters with 28 and 29 Ti atoms as well as a new dopant-free Ti28 cluster are presented. The light-metal-doped polyoxotitanate clusters in which the alkali-metal atom is the critical structure-determining component are the largest synthesized so far. Calculations show that doping with light alkali atoms narrows the band gap compared with the nondoped crystals but does not introduce additional energy levels within the band gap.

  14. Aluminium hydroxide-induced granulomas in pigs

    DEFF Research Database (Denmark)

    Valtulini, S; Macchi, C; Ballanti, P


    The effect of intramuscular injection of 40 mg/2 ml aluminium hydroxide in the neck of pigs was examined in a number of ways. The investigation followed repeated slaughterhouse reports, according to which 64.8% of pigs from one particular farm were found at slaughter to have one or more nodules...... in the muscles of the neck (group slaughtered). The pigs had been injected with a vaccine containing 40 mg/2 ml dose of aluminium hydroxide as adjuvant. Research consisted of two phases: first, an epidemiological study was carried out, aimed at determining the risk factors for the granulomas. The results...... and adjuvant) to pigs inoculated twice with apyrogenic bi-distilled water (group water) and to pigs inoculated once with the adjuvant and once with apyrogenic bi-distilled water (group adjuvant/water). Both studies agreed in their conclusions, which indicate that the high amount of aluminium hydroxide...

  15. Surface Acidity of Amorphous Aluminum Hydroxide

    Institute of Scientific and Technical Information of China (English)



    The surface acidity of synthetic amorphous Al hydroxide was determined by acid/base titration with several complementary methods including solution analyses of the reacted solutions and XRD characterization of the reacted solids. The synthetic specimen was characterized to be the amorphous material showing four broad peaks in XRD pattern. XRD analyses of reacted solids after the titration experiments showed that amorphous Al hydroxide rapidly transformed to crystalline bayerite at the alkaline condition (pH>10). The solution analyses after and during the titration experiments showed that the solubility of amorphous aluminum hydroxide, Ksp =aAl3+/a3H+,was 1010.3,The amount of consumption of added acid or base during the titration experiment was attributed to both the protonation/deprotonation of dissolved Al species and surface hydroxyl group. The surface acidity constants, surface hydroxyl density and specific surface area were estimated by FITEQL 4.0.

  16. Relaxation of quadrupole orientation in an optically pumped alkali vapour

    Energy Technology Data Exchange (ETDEWEB)

    Bernabeu, E.; Tornos, J.


    The relaxation of quadrupole orientation (alignment) in an optically pumped alkali vapour is theoretically studied by taking into account the relaxation processes by alkali-buffer gas, alkali-alkali with spin exchange and alkali-cell wall (diffusion process) collisions. The relaxation transients of the quadrupole orientation are obtained by introducing a first-order weak-pumping approximation (intermediate pumping) less restrictive than the usually considered (zeroth order) one.

  17. Milk Alkali and Hydrochlorothiazide: A Case Report

    Directory of Open Access Journals (Sweden)

    Babar Parvez


    Full Text Available Hypercalcemia is a relatively common clinical problem in both outpatient and inpatient settings. Primary pathophysiology is the entry of calcium that exceeds its excretion into urine or deposition in bone into circulation. Among a wide array of causes of hypercalcemia, hyperparathyroidism and malignancy are the most common, accounting for greater than 90 percent of cases. Concordantly, there has been a resurgence of milk-alkali syndrome associated with the ingestion of large amounts of calcium and absorbable alkali, making it the third leading cause of hypercalcemia (Beall and Scofield, 1995 and Picolos et al., 2005. This paper centers on a case of over-the-counter calcium and alkali ingestion for acid reflux leading to milk alkali with concordant use of thiazide diuretic for hypertension.

  18. Alkali activation of recovered fuel-biofuel fly ash from fluidised-bed combustion: Stabilisation/solidification of heavy metals. (United States)

    Yliniemi, Juho; Pesonen, Janne; Tiainen, Minna; Illikainen, Mirja


    Recovered fuel-biofuel fly ash from a fluidized bed boiler was alkali-activated and granulated with a sodium-silicate solution in order to immobilise the heavy metals it contains. The effect of blast-furnace slag and metakaolin as co-binders were studied. Leaching standard EN 12457-3 was applied to evaluate the immobilisation potential. The results showed that Ba, Pb and Zn were effectively immobilised. However, there was increased leaching after alkali activation for As, Cu, Mo, Sb and V. The co-binders had minimal or even negative effect on the immobilisation. One exception was found for Cr, in which the slag decreased leaching, and one was found for Cu, in which the slag increased leaching. A sequential leaching procedure was utilized to gain a deeper understanding of the immobilisation mechanism. By using a sequential leaching procedure it is possible fractionate elements into watersoluble, acid-soluble, easily-reduced and oxidisable fractions, yielding a total 'bioavailable' amount that is potentially hazardous for the environment. It was found that the total bioavailable amount was lower following alkali activation for all heavy metals, although the water-soluble fraction was higher for some metals. Evidence from leaching tests suggests the immobilisation mechanism was chemical retention, or trapping inside the alkali activation reaction products, rather than physical retention, adsorption or precipitation as hydroxides.

  19. Layered double hydroxide stability. 1. Relative stabilities of layered double hydroxides and their simple counterparts (United States)

    Boclair, J. W.; Braterman, P. S.


    Solutions containing di- and trivalent metal chlorides [M(II) = Mg2+, Zn2+, Co2+, Ni2+, Mn2+; M(III) = Al3+, Fe3+] were titrated with NaOH to yield hydrotalcite-like layered double hydroxides (LDH), [[M(II)]1-x[M(III)]x(OH)2][Cl]x yH2O, by way of M(III) hydroxide/hydrous oxide intermediates. Analysis of the resultant titration curves yields nominal solubility constants for the LDH. The corresponding LDH stabilities are in the order Mg hydroxides/hydrous oxides is discussed.

  20. Silver Orthophosphate Immobilized on Flaky Layered Double Hydroxides as the Visible-Light-Driven Photocatalysts

    Directory of Open Access Journals (Sweden)

    Xianlu Cui


    Full Text Available Flaky layered double hydroxide (FLDH was prepared by the reconstruction of its oxide in alkali solution. The composites with FLDH/Ag3PO4 mass ratios at 1.6 : 1 and 3 : 1 were fabricated by the coprecipitation method. The powders were characterized by X-ray diffraction, field-emission scanning electron microscopy, transmission electron microscope, and UV-vis diffuse reflectance spectroscopy. The results indicated that the well-distributed Ag3PO4 in a fine crystallite size was formed on the surface of FLDH. The photocatalytic activities of the Ag3PO4 immobilized on FLDH were significantly enhanced for the degradation of acid red G under visible light irradiation compared to bare Ag3PO4. The composite with the FLDH/Ag3PO4 mass ratio of 3 : 1 showed a higher photocatalytic efficiency.

  1. The effect of calcium hydroxide treatment on the nutritive and feeding value of Albizia procera for growing goats

    Energy Technology Data Exchange (ETDEWEB)

    Alam, M.R. [Department of Animal Science, Bangladesh Agricultural University, Mymensingh (Bangladesh)]. E-mail:; Kabir, A.K.M.A.; Amin, M.R. [Department of Animal Science, Bangladesh Agricultural University, Mymensingh (Bangladesh); McNeill, D.M. [Faculty of Veterinary Science, University of Sydney, Camden, NSW (Australia)


    Albizia procera (Albizia) is widely planted in Bangladesh for timber and the leaves are also used as forage. In the dry season the leaves are less palatable than in the wet season and this may be a consequence of an excessive content of tannin. Albizia foliage was collected in the wet (June) and dry (January) seasons from six agro-ecological zones across Bangladesh and chemical composition, for tannins in particular, was determined. Variation in the tannin content across the six zones proved to be minimal. However, the concentration of tannins was almost two-fold higher in the dry compared to the wet season. To assess the potential for deactivating the tannins in Albizia so as to improve its nutritive value, leaves were treated with alkali (either calcium hydroxide or potassium carbonate) or polyethylene glycol (PEG). Alkali treatment reduced the concentrations of extractable tannin by as much as 92%. The ability of calcium hydroxide to deactivate tannin was then tested in vivo. Young goats, fed a basal diet of hay and wheat bran, were allocated to 4 equal groups (n = 4 per group) and supplemented with fresh Albizia foliage (at 300 g/kg of the diet) that was either untreated, or treated with either PEG, calcium hydroxide or calcium hydroxide + PEG. The supplements were fed daily for 9 weeks to allow the effects of chemical treatment on intake and growth rate to be defined. In vivo digestibility, nitrogen (N) balance, and microbial N supply were measured over the 5th week. Intakes of feed dry matter (DM) and the digestibility of DM were similar across treatments (mean intake 32 g/(kg LW day), mean DM digestibility 0.63). However, both the PEG and the PEG + calcium hydroxide treatments, compared to the control and calcium hydroxide only treatments, increased N digestibility (0.72, 0.70 versus 0.60, 0.61), N retention (0.43, 0.48 mg N/mg versus 0.26, 0.27 mg N/mg N intake), and microbial N supply (23.7, 21.4 g/day versus 14.2, 12.4 g/day). These increases translated

  2. Structural transformation of nickel hydroxide films during anodic oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Crocker, R.W.; Muller, R.H.


    The transformation of anodically formed nickel hydroxide/oxy-hydroxide electrodes has been investigated. A mechanism is proposed for the anodic oxidation reaction, in which the reaction interface between the reduced and oxidized phases of the electrode evolves in a nodular topography that leads to inefficient utilization of the active electrode material. In the proposed nodular transformation model for the anodic oxidation reaction, nickel hydroxide is oxidized to nickel oxy-hydroxide in the region near the metal substrate. Since the nickel oxy-hydroxide is considerably more conductive than the surrounding nickel hydroxide, as further oxidation occurs, nodular features grow rapidly to the film/electrolyte interface. Upon emerging at the electrolyte interface, the reaction boundary between the nickel hydroxide and oxy-hydroxide phases spreads laterally across the film/electrolyte interface, creating an overlayer of nickel oxy-hydroxide and trapping uncharged regions of nickel hydroxide within the film. The nickel oxy-hydroxide overlayer surface facilitates the oxygen evolution side reaction. Scanning tunneling microscopy of the electrode in its charged state revealed evidence of 80 {endash} 100 Angstrom nickel oxy-hydroxide nodules in the nickel hydroxide film. In situ spectroscopic ellipsometer measurements of films held at various constant potentials agree quantitatively with optical models appropriate to the nodular growth and subsequent overgrowth of the nickel oxy-hydroxide phase. A two-dimensional, numerical finite difference model was developed to simulate the current distribution along the phase boundary between the charged and uncharged material. The model was used to explore the effects of the physical parameters that govern the electrode behavior. The ratio of the conductivities of the nickel hydroxide and oxy-hydroxide phases was found to be the dominant parameter in the system.

  3. Single sheet metal oxides and hydroxides

    DEFF Research Database (Denmark)

    Huang, Lizhi

    The synthesis of layered double hydroxides (LDHs) provides a relatively easy and traditional way to build versatile chemical compounds with a rough control of the bulk structure. The delamination of LDHs to form their single host layers (2D nanosheets) and the capability to reassemble them offer ...

  4. Hydroxide catalysis bonding of silicon carbide

    NARCIS (Netherlands)

    Veggel, A.A. van; Ende, D.A. van den; Bogenstahl, J.; Rowan, S.; Cunningham, W.; Gubbels, G.H.M.; Nijmeijer, H.


    For bonding silicon carbide optics, which require extreme stability, hydroxide catalysis bonding is considered [Rowan, S., Hough, J. and Elliffe, E., Silicon carbide bonding. UK Patent 040 7953.9, 2004. Please contact Mr. D. Whiteford for further information:]. This techn

  5. Polysulfide intercalated layered double hydroxides for metal capture applications

    Energy Technology Data Exchange (ETDEWEB)

    Kanatzidis, Mercouri G.; Ma, Shulan


    Polysulfide intercalated layered double hydroxides and methods for their use in vapor and liquid-phase metal capture applications are provided. The layered double hydroxides comprise a plurality of positively charged host layers of mixed metal hydroxides separated by interlayer spaces. Polysulfide anions are intercalated in the interlayer spaces.

  6. Methotrexatum intercalated layered double hydroxides: statistical design, mechanism explore and bioassay study. (United States)

    Wang, Xiao-Feng; Liu, Su-Qing; Li, Shu-Ping


    A series of methotrexatum intercalated layered double hydroxide (MTX/LDH for short) hybrids have been synthesized by a mechanochemical-hydrothermal method, the statistical experiments are planned and conducted to find out the critical factor influencing the physicochemical properties. Four variables, i.e., addition of NaOH solution, grinding duration, hydrothermal temperature and time, are chosen to play as the examined factors in the orthogonal design. Furthermore, three respective levels, i.e., high, medium and low levels, are conducted in the design. The resulting hybrids are then characterized by X-ray diffraction (XRD) patterns, transmission electron microscope (TEM) graphs and Zeta potentials. XRD diffractions indicate that MTX anions have been successfully intercalated into LDH interlayers and the amount of NaOH solution can change the gallery height greatly. The information from TEM graphs and Zeta potentials state that the increase of alkali solution gives rise to regular morphology and the increase of Zeta potentials. As a result of the statistical analysis, addition of alkali solution is the major factor affecting the morphology and drug-loading capacity. At last, the mechanism of particle growth is explored emphatically, and the anticancer efficacy of some MTX/LDH hybrids is estimated by MTT assay on A549 cells as well.

  7. Pilot-scale production of biodiesel from waste fats and oils using tetramethylammonium hydroxide. (United States)

    Šánek, Lubomír; Pecha, Jiří; Kolomazník, Karel; Bařinová, Michaela


    Annually, a great amount of waste fats and oils not suitable for human consumption or which cannot be further treated are produced around the world. A potential way of utilizing this low-cost feedstock is its conversion into biodiesel. The majority of biodiesel production processes today are based on the utilization of inorganic alkali catalysts. However, it has been proved that an organic base - tetramethylammonium hydroxide - can be used as a very efficient transesterification catalyst. Furthermore, it can be employed for the esterification of free fatty acids - reducing even high free fatty acid contents to the required level in just one step. The work presented herein, is focused on biodiesel production from waste frying oils and animal fats using tetramethylammonium hydroxide at the pilot-plant level. The results showed that the process performance in the pilot unit - using methanol and TMAH as a catalyst, is comparable to the laboratory procedure, even when the biodiesel is produced from waste vegetable oils or animal fats with high free fatty acid content. The reaction conditions were set at: 1.5% w/w of TMAH, reaction temperature 65°C, the feedstock to methanol molar ratio to 1:6, and the reaction time to 120min. The conversion of triglycerides to FAME was approximately 98%. The cloud point of the biodiesel obtained from waste animal fat was also determined.

  8. Methotrexatum intercalated layered double hydroxides: Statistical design, mechanism explore and bioassay study

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xiao-Feng [Department of Gastroenterology, Weihai municipal hospital, Weihai 264200 (China); Liu, Su-Qing [Jiangsu Key Laboratory of Biofunctional Material, College of Chemistry and Material Science, Nanjing Normal University, Nanjing 210023 (China); Li, Shu-Ping, E-mail: [Jiangsu Key Laboratory of Biofunctional Material, College of Chemistry and Material Science, Nanjing Normal University, Nanjing 210023 (China)


    A series of methotrexatum intercalated layered double hydroxide (MTX/LDH for short) hybrids have been synthesized by a mechanochemical–hydrothermal method, the statistical experiments are planned and conducted to find out the critical factor influencing the physicochemical properties. Four variables, i.e., addition of NaOH solution, grinding duration, hydrothermal temperature and time, are chosen to play as the examined factors in the orthogonal design. Furthermore, three respective levels, i.e., high, medium and low levels, are conducted in the design. The resulting hybrids are then characterized by X-ray diffraction (XRD) patterns, transmission electron microscope (TEM) graphs and Zeta potentials. XRD diffractions indicate that MTX anions have been successfully intercalated into LDH interlayers and the amount of NaOH solution can change the gallery height greatly. The information from TEM graphs and Zeta potentials state that the increase of alkali solution gives rise to regular morphology and the increase of Zeta potentials. As a result of the statistical analysis, addition of alkali solution is the major factor affecting the morphology and drug-loading capacity. At last, the mechanism of particle growth is explored emphatically, and the anticancer efficacy of some MTX/LDH hybrids is estimated by MTT assay on A549 cells as well. - Graphical abstract: Schematic illustration of synthesis and properties of MTX intercalated LDH hybrids. - Highlights: • Increasing NaOH solution gives rise to high drug-loading capacity. • Increasing the alkali solution leads to high layer charge and regular morphology. • The monodispersity has critical effect on the tumor suppression efficiency.

  9. Growth of bacteria and yeast on enzymically degraded alkali treated rice and wheat straws

    Energy Technology Data Exchange (ETDEWEB)

    Gupta, J.K.; Shirkot, C.K.; Dhawan, S.


    An enzyme filtrate of Trichoderma viride QM 9414 was used to saccharify rice and wheat straw. Delignification of the straw by alkali treatment increased the enzymic saccharification of both materials to approximately 70%. The optimum conditions for delignification were autoclaving at 120 degrees for 30 minutes with 2% Sodium Hydroxide. Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, Lactobacillus acidophilus, Bacillus megaterium, and Saccharomyces cerevisiae grew very well on enriched hydrolyzates of rice and wheat straws. Even nonenriched straw hydrolyzates supported better growth of L. acidophilus, B. megaterium, and E. coli on rice straw than the enriched synthetic medium containing equivalent glucose. S. cerevisiae grown in shake flasks containing 25 mL of enriched rice and wheat straw hydrolyzates yielded 0.595 g and 0.450 g of dry cells, respectively. The corresponding yield was 0.396 g from enriched synthetic medium containing equal amounts of glucose.

  10. Characterization of polysaccharides extracted from spent coffee grounds by alkali pretreatment. (United States)

    Ballesteros, Lina F; Cerqueira, Miguel A; Teixeira, José A; Mussatto, Solange I


    Spent coffee grounds (SCG), obtained during the processing of coffee powder with hot water to make soluble coffee, are the main coffee industry residues and retain approximately seventy percent of the polysaccharides present in the roasted coffee beans. The purpose of this study was to extract polysaccharides from SCG by using an alkali pretreatment with sodium hydroxide at 25°C, and determine the chemical composition, as well as the antioxidant and antimicrobial properties of the extracted polysaccharides. Galactose (60.27%mol) was the dominant sugar in the recovered polysaccharides, followed by arabinose (19.93%mol), glucose (15.37%mol) and mannose (4.43%mol). SCG polysaccharides were thermostable, and presented a typical carbohydrate pattern. Additionally, they showed good antioxidant activity through different methods and presented high antimicrobial percent inhibition against Phoma violacea and Cladosporium cladosporioides (41.27% and 54.60%, respectively). These findings allow identifying possible applications for these polysaccharides in the food industry.

  11. Selection of non-adsorbing alkali components

    Energy Technology Data Exchange (ETDEWEB)

    Lee, S.H.D.; Natesan, K.; Swift, W.M.


    This project consists of three phases of laboratory experimental study. In phase I (screening), eight candidate materials, 304SS (serves as a base material for comparison), Hastelloy C-276, Hastelloy X, Haynes No. 188, Allonized 304SS, Pt-coated 304SS, and ceramic-coated 304SS, will be subjected to atmospheric TGA study under the simulated PFBC (oxidizing) environment with and without alkali vapor doping. Each candidate material will be evaluated for its resistance toward alkali-vapor capture. In addition, a post-test metallographic characterization of the sample will be performed to obtain a better understanding of the alkali capture mechanism and material behavior. The material(s) with little or no alkali-vapor adsorption will be selected as the promising material(s) for the Phase II study. In Phase II, the promising material(s) will be further tested in the TGA under elevated pressure to simulate the PFBC environment (in terms of temperature, pressure, and gas composition). The effect of pressure on the extent of alkali-vapor adsorption will be evaluated, and the test samples will be metallographically characterized. The most promising candidate material(s) will be identified and recommended for further tesfing in the actual PFBC environment. In Phase III, four materials will be selected from the eight candidate materials screened in the PFBC environment and will be evaluated for their alkali-vapor capture by atmospheric TGA under the coal gasification fuel gas (reducing) environment. The tested samples will also be metallographically characterized. The most promising material(s) will be identified and recommended for further testing in the actual coal gasification environment.

  12. Selection of non-adsorbing alkali components

    Energy Technology Data Exchange (ETDEWEB)

    Lee, S.H.D.; Natesan, K.; Swift, W.M.


    This project consists of three phases of laboratory experimental study. In phase I (screening), eight candidate materials, 304SS (serves as a base material for comparison), Hastelloy C-276, Hastelloy X, Haynes No. 188, Allonized 304SS, Pt-coated 304SS, and ceramic-coated 304SS, will be subjected to atmospheric TGA study under the simulated PFBC (oxidizing) environment with and without alkali vapor doping. Each candidate material will be evaluated for its resistance toward alkali-vapor capture. In addition, a post-test metallographic characterization of the sample will be performed to obtain a better understanding of the alkali capture mechanism and material behavior. The material(s) with little or no alkali-vapor adsorption will be selected as the promising material(s) for the Phase II study. In Phase II, the promising material(s) will be further tested in the TGA under elevated pressure to simulate the PFBC environment (in terms of temperature, pressure, and gas composition). The effect of pressure on the extent of alkali-vapor adsorption will be evaluated, and the test samples will be metallographically characterized. The most promising candidate material(s) will be identified and recommended for further tesfing in the actual PFBC environment. In Phase III, four materials will be selected from the eight candidate materials screened in the PFBC environment and will be evaluated for their alkali-vapor capture by atmospheric TGA under the coal gasification fuel gas (reducing) environment. The tested samples will also be metallographically characterized. The most promising material(s) will be identified and recommended for further testing in the actual coal gasification environment.

  13. Optimization of alkaline sulfite pretreatment and comparative study with sodium hydroxide pretreatment for improving enzymatic digestibility of corn stover. (United States)

    Liu, Huan; Pang, Bo; Wang, Haisong; Li, Haiming; Lu, Jie; Niu, Meihong


    In this study, alkaline sulfite pretreatment of corn stover was optimized. The influences of pretreatments on solid yield, delignification, and carbohydrate recovery under different pretreatment conditions and subsequent enzymatic hydrolysis were investigated. The effect of pretreatment was evaluated by enzymatic hydrolysis efficiency and the total sugar yield. The optimum pretreatment conditions were obtained, as follows: the total titratable alkali (TTA) of 12%, liquid/solid ratio of 6:1, temperature of 140 °C, and holding time of 20 min. Under those conditions, the solid yield was 55.24%, and the removal of lignin was 82.68%. Enzymatic hydrolysis rates of glucan and xylan for pretreated corn stover were 85.38% and 70.36%, and the total sugar yield was 74.73% at cellulase loading of 20 FPU/g and β-glucosidase loading of 10 IU/g for 48 h. Compared with sodium hydroxide pretreatment with the same amount of total titratable alkali, the total sugar yield was raised by about 10.43%. Additionally, the corn stover pretreated under the optimum pretreatment conditions was beaten by PFI at 1500 revolutions. After beating, enzymatic hydrolysis rates of glucan and xylan were 89.74% and 74.06%, and the total sugar yield was 78.58% at the same enzymatic hydrolysis conditions. Compared with 1500 rpm of PFI beating after sodium pretreatment with the same amount of total titratable alkali, the total sugar yield was raised by about 14.05%.

  14. Layered Double Hydroxide as Cordycepin Delivery Nanocarrier

    Institute of Scientific and Technical Information of China (English)

    Qin Zheng YANG; Jing YANG; Chang Kai ZHANG


    Layered double hydroxide was investigated as cordycepin delivery nanocarrier for the first time in this study. Negatively charged biomolecule-cordycepin was intercalated in the gallery spaces of [Mg-Al-NO3], which was confirmed by the results of X-ray diffraction and electrophoretic mobility. Cell experiment suggested that the new bio-LDH nanohybrid could prevent cordycepin decomposition by adenosine deaminase. This new formulation could possibly be used as a novel form cordycepin intravenous injection.

  15. Thermal behaviour of hydroxides, hydroxysalts and hydrotalcites

    Indian Academy of Sciences (India)

    Parthasarathi Bera; Michael Rajamathi; M S Hegde; P Vishnu Kamath


    Mass spectrometric analysis of gases evolved during thermal decomposition of divalent metal hydroxides, hydroxysalts and hydrotalcites show that all these compounds undergo dehydration in the temperature range 30 < T < 220°C followed by decomposition at temperatures above 250°C. The latter step involves simultaneous deanation and dehydroxylation of the layers. Our observations conclusively prove that alternative mechanisms which envisage CO2 evolution due to deanation at lower temperatures proposed by Kanezaki to be wrong.

  16. Nickel hydroxide modified electrodes for urea determination

    Directory of Open Access Journals (Sweden)

    Luiz Henrique Dall´Antonia


    Full Text Available Nickel hydroxide films were prepared by electrodeposition from a solution Ni(NO32 0,05 mol L ?¹ on ITO electrodes (Tin oxide doped with Indium on PET-like plastic film, applying a current of - 0,1 A cm ?² during different time intervals between 1800 and 7200 s. The electrochemical behavior of the nickel hydroxide electrode was investigated through a cyclic voltammogram, in NaOH 1,0 mol L ?¹, where it was observed two peaks in the profile in 0,410 and 0,280 V, corresponding to redox couple Ni(II/Ni(III. A sensor for urea presenting a satisfactory answer can be obtained when, after the deposit of the film of Ni(OH2 on the electrode of nickel, it is immersed in a solution of NaOH 1,0 mol L ?¹ and applying a potential of + 0,435 V, where the maximum of the anodic current occurs in the cyclic voltammogram. Analyzing the results it can be observed that, for a range of analite concentration between 5 to 50 m mol L ?¹, the behavior is linear and the sensibility found was of 20,3 mA cm?² (mol L?¹?¹, presenting reproducibility confirming the nickel hydroxide electrodes utilization for the determination of urea.

  17. Effect of three different calcium hydroxide mixtures (calcium hydroxide with glycerine, normal saline and distilled water on root dentin microhardness

    Directory of Open Access Journals (Sweden)

    Hasheminia SM


    Full Text Available Background and Aim: During root canal therapy, it is necessary to remove as many bacteria as possible from the root canal. The use of medicaments is recommended to reduce the microbial population prior to root filling. Calcium hydroxide pastes have been used because of their antibacterial effects and the ability of tissue dissolving. The aim of this study was to evaluate the effect of calcium hydroxide/glycerine mixture, calcium hydroxide/normal saline mixture and calcium hydroxide/distilled water mixture on root dentin microhardness in storage times of 7 and 14 days.Materials and Methods: In this in vitro study, fifteen extracted maxillary canines and central incisors were selected. The crowns of the teeth were removed and the canals were prepared. Teeth were sectioned transversally to produce a total of 30 dentin discs from the middle third of the roots. Specimens were divided into three groups of 10 discs each. Dentin samples were subjected to calcium hydroxide/glycerine, calcium hydroxide/normal saline and calcium hydroxide/distilled water mixtures for 7 and 14 days. Dentin microhardness was measured by a Vickers indenter with a load of 200 g for 15 seconds. Data were analyzed using ANOVA, Paired t-test and LSD with p<0.05 as the level of significance.Results: Statistical analysis showed that all three mixtures decreased dentin microhardness. After 7 days, reduction in dentin microhardness by calcium hydroxide/glycerine combination was significantly higher than calcium hydroxide/normal saline and calcium hydroxide/distilled water combinations. After 14 days, reduction in dentin microhardness by calcium hydroxide/distilled water combination was significantly higher than the other two groups.Conclusion: Based on the results of this study, the use of calcium hydroxide combinations for intracanal dressing reduces dentin microhardness. After 7 days calcium hydroxide/glycerine combination and after 14 days calcium hydroxide/distilled water

  18. Positronium impact ionization of Alkali atoms

    CERN Document Server

    Ghosh, D


    Target ionization processes of alkali atoms by Positronium impact are investigated. Calculations are performed in the frame work of model potential formalism using the Coulomb distorted eikonal approximation. Interesting qualitative features are noted both in the scattered Ps and the ejected electron distributions in differential as well as double differential levels of the collision cross sections.

  19. Microwave Assisted Alkali Pretreatment of Rice Straw for Enhancing Enzymatic Digestibility

    Directory of Open Access Journals (Sweden)

    Renu Singh


    Full Text Available Rapid industrialization, increasing energy demand, and climate change are the conditions that forced the researchers to develop a clean, efficient, renewable, and sustainable source of energy which has a potential to replace fossil fuels. Ethanol is one of the attractive and suitable renewable energy resources. In present study, effectiveness of microwave pretreatment in combination with sodium hydroxide (NaOH for increasing enzymatic hydrolysis of rice straw has been investigated and under optimum conditions obtained a maximum reducing sugar (1334.79 µg/mL through microwave assisted NaOH pretreatment. Chemical composition analysis and scanning electron microscope (SEM images showed that the removal of lignin, hemicellulose, and silicon content is more in microwave assisted NaOH pretreatment than the blank sample. X-ray diffraction (XRD analysis revealed that the crystallinity index of rice straw treated with microwave assisted alkali (54.55% is significantly high as compared to the blank (49.07%. Hence, the present study proves that microwave assisted alkali pretreatment can effectively enhance enzymatic digestibility of rice straw and it is feasible to convert rice straw for bioethanol production.

  20. High pressure assist-alkali pretreatment of cotton stalk and physiochemical characterization of biomass. (United States)

    Du, Shuang-kui; Zhu, Xinna; Wang, Hua; Zhou, Dayun; Yang, Weihua; Xu, Hongxia


    Ground cotton stalks were pretreated with sodium hydroxide (NaOH) at concentrations of 1-4% (w/v), pressures of 30-130 kPa, durations of 15-75 min, and liquid/solid ratios of 10:1-30:1. Modeling of the high pressure assist-alkali pretreatment (HPAP) of cotton stalk was attempted. The levels of NaOH concentration, pressure, and duration were optimized using a Box-Behnken design to enhance the cellulose content of treated solid residue. The optimum pretreatment conditions were as follows: liquid/solid ratio, 20:1; pressure, 130 kPa; NaOH concentration, 3.0%; duration, 40 min. During the conditions, cellulose content of pretreated cotton stalk residue was 64.07%. The maximum cellulose conversion of 45.82% and reducing sugar yield of 0.293 g/g upon hydrolysis were obtained. Significant differences were observed in biomass composition and physiochemical characteristics between native and alkali-treated biomass. High NaOH concentration and pressure were conducive to lignin dissolution and resulted in increased cellulose content and conversion.

  1. Monitoring, Modeling, and Diagnosis of Alkali-Silica Reaction in Small Concrete Samples

    Energy Technology Data Exchange (ETDEWEB)

    Agarwal, Vivek [Idaho National Lab. (INL), Idaho Falls, ID (United States); Cai, Guowei [Idaho National Lab. (INL), Idaho Falls, ID (United States); Gribok, Andrei V. [Idaho National Lab. (INL), Idaho Falls, ID (United States); Mahadevan, Sankaran [Idaho National Lab. (INL), Idaho Falls, ID (United States)


    Assessment and management of aging concrete structures in nuclear power plants require a more systematic approach than simple reliance on existing code margins of safety. Structural health monitoring of concrete structures aims to understand the current health condition of a structure based on heterogeneous measurements to produce high-confidence actionable information regarding structural integrity that supports operational and maintenance decisions. This report describes alkali-silica reaction (ASR) degradation mechanisms and factors influencing the ASR. A fully coupled thermo-hydro-mechanical-chemical model developed by Saouma and Perotti by taking into consideration the effects of stress on the reaction kinetics and anisotropic volumetric expansion is presented in this report. This model is implemented in the GRIZZLY code based on the Multiphysics Object Oriented Simulation Environment. The implemented model in the GRIZZLY code is randomly used to initiate ASR in a 2D and 3D lattice to study the percolation aspects of concrete. The percolation aspects help determine the transport properties of the material and therefore the durability and service life of concrete. This report summarizes the effort to develop small-size concrete samples with embedded glass to mimic ASR. The concrete samples were treated in water and sodium hydroxide solution at elevated temperature to study how ingress of sodium ions and hydroxide ions at elevated temperature impacts concrete samples embedded with glass. Thermal camera was used to monitor the changes in the concrete sample and results are summarized.

  2. Alkali-treated konjac glucomannan film as a novel wound dressing. (United States)

    Huang, Yi-Cheng; Chu, Hao-Wen; Huang, Chih-Ching; Wu, Wen-Ching; Tsai, Jenn-Shou


    To investigate the potential medical application of konjac glucomannan (KGM), we treated KGM film with potassium hydroxide (KOH) or calcium hydroxide (Ca(OH)2), and evaluated its use as a wound dressing. The Ca(OH)2-treated KGM (Ca(OH)2-KGM) film exhibited more favorable properties of swelling, tensile strength, and elongation compared with the KOH-treated KGM (KOH-KGM) film, and also had a suitable water vapor transmission rate. Results from in vitro 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay further indicated the biocompatibility of the Ca(OH)2-KGM film with L929 fibroblast cells and HaCaT keratinocyte cells. The Ca(OH)2-KGM film inhibited the absorption and activation of platelets, and effectively promoted wound contractility in vivo, particularly at an early healing stage. Histological examination revealed considerably collagen secretion and advanced development of granulation tissue and epithelial coverage by Days 7 and 14 postsurgery in wounds treated with Ca(OH)2-KGM film. Our study results indicate the potential use of alkali-treated KGM film as a novel wound dressing.

  3. Pulp response to a novel adhesive calcium hydroxide based cement. (United States)

    Watts, A; Paterson, R C; Cohen, B D; Combe, E C


    This study compares pulp responses to 3 formulations of calcium hydroxide, namely: a) An experimental adhesive calcium hydroxide cement containing polyacrylic acid, b) Dycal (L.D> Caulk Co, Milford, Delaware) Batch Nos 176970/176990, c) "Analar" calcium hydroxide mixed with sterile distilled water. After 28 days dentine bridges were present in 77% of teeth capped with the test material, 64% of teeth treated with Dycal and in 62% of teeth capped with calcium hydroxide and water. Inflammatory infiltrates were observed in a number of teeth remote from the bridges. Bacteria were detected in these specimens. Exposed rat molar pulp responses to an experimental adhesive calcium hydroxide cement were similar to to those observed with 2 other calcium hydroxide formulations.

  4. Polytypic transformations of aluminum hydroxide: A mechanistic investigation

    Institute of Scientific and Technical Information of China (English)

    Thimmasandra Narayan Ramesh


    The diffusion of ammonia vapors into a solution of aluminum nitrate or ferric nitrate results in the precipitation of their respective hydroxides and oxyhydroxides.Polymorphic phase formation of aluminum hydroxide is controlled by the rate of crystallization.The PXRD patterns of products obtained via vapor phase diffusion revealed that poorly ordered aluminum hydroxide is formed during the initial stages of crystallization.After 8 days,the formation of the bayerite phase of aluminum hydroxide was observed.Upon prolonged exposure to ammonia vapors,bayerite was transformed into gibbsite.The infrared spectrum of the product confirmed the presence of different polytypic phases of aluminum hydroxide.The results demonstrated that the crystal structure of metal hydroxides is controlled by the rate of crystallization,nature of the metal ion,site selectivity and specificity and preparative conditions.

  5. Effect of Grain Size and Reaction Time in Characterisation of Aggregates for Alkali Silica Reaction Using Chemical Method

    Directory of Open Access Journals (Sweden)

    R.P. Pathak


    Full Text Available Concrete can deteriorate as a result of alkali aggregate reaction, an interaction between alkalis present in alkaline pore solution originating from the Portland cement and reactive minerals in certain types of aggregates. Potential reactivity of aggregates with regard to alkalis present in concrete mix can be determined by Mortar Bar method, Chemical Method and Petrographic analysis. Of these the chemical method though is quick and does not require a large quantity of material for testing yet have its own inherent limitations. It does not ensure completion of reaction as the observations are limited to 24hour only and also does not assess the effect of varying the combination of coarse and fine aggregates. A study on chemical method by allowing the reaction for a prolonged time up to 96 hours and also on different grain size ranged matrix was carried at Central Soil and Materials Research Station, New Delhi. Simultaneously the test results of the modified method are compared to the existing Mortar Bar method, Chemical Method and Petrographic analysis The outcome of the studies clearly reflects that the grain size play an important role in the reaction, the reaction time has a demarked impact on reactivity, in the cases having a high value of silica release the choice of reduction in alkalinity as an indicator of degree of reaction is not reliable, instead measuring remaining Na2O concentration in Sodium hydroxide solution after the reaction seems to be much more meaningful in justifying the silica release.

  6. Local structure of alkalis in mixed-alkali borate glass to elucidate the origin of mixed-alkali effect

    Directory of Open Access Journals (Sweden)

    Yomei Tokuda


    Full Text Available We report the structural analysis of Na+ and Cs+ in sodium cesium borate crystals and glasses using 23Na and 133Cs magic-angle spinning nuclear magnetic resonance (MAS NMR spectroscopy. The composition dependence of NMR spectra of the borate was similar to that of the silicate: (1 the peak position of cesium borate crystals shifted to upfield for structures with larger Cs+ coordination numbers, (2 the MAS NMR spectra of xNa2O-yCs2O-3B2O3 (x = 0, 0.25, 0.5, 0.75, 1.0, x + y = 1 glass showed that the average coordination number (CN of both the alkali cations decreases with increasing Cs+/(Na+ + Cs+ ratio. However, the degree of decrement in borates is much smaller than that in silicates. We have considered that the small difference in CN is due to 4-coordinated B, because it is electrically compensated by the alkali metal ions resulting in the restriction of having various coordinations of O to alkali metal.

  7. The impact of alkali pretreatment and post-pretreatment conditioning on the surface properties of rice straw affecting cellulose accessibility to cellulases. (United States)

    Karuna, Nardrapee; Zhang, Lu; Walton, Jeffrey H; Couturier, Marie; Oztop, Mecit H; Master, Emma R; McCarthy, Michael J; Jeoh, Tina


    Rice straw was pretreated with sodium hydroxide and subsequently conditioned to reduce the pH to 5-6 by either: (1) extensive water washing or (2) acidification with hydrochloric acid then water washing. Alkali pretreatment improved the enzymatic digestibility of rice straw by increasing the cellulose accessibility to cellulases. However, acidification after pretreatment reversed the gains in cellulose accessibility to cellulases and enzymatic digestibility due to precipitation of solubilized compounds. Surface composition analyses by ToF-SIMS confirmed a reduction in surface lignin by pretreatment and water washing, and suggested that acidification precipitated a chemically modified form of lignin on the surfaces of rice straw. The spin-spin relaxation times (T2) of the samples indicated increased porosity in alkali pretreated rice straw. The acidified pretreated rice straw had reduced amounts of water in the longer T2 proton pools associated with water in the pores of the biomass likely due to back-filling by the precipitated components.

  8. Removal of Retired Alkali Metal Test Systems

    Energy Technology Data Exchange (ETDEWEB)

    Brehm, W. F.; Church, W. R.; Biglin, J. W.


    This paper describes the successful effort to remove alkali metals, alkali metal residues, and piping and structures from retired non-radioactive test systems on the Hanford Site. These test systems were used between 1965 and 1982 to support the Fast Flux Test Facility and the Liquid Metal Fast Breeder Reactor Program. A considerable volume of sodium and sodium-potassium alloy (NaK) was successfully recycled to the commercial sector; structural material and electrical material such as wiring was also recycled. Innovative techniques were used to safely remove NaK and its residues from a test system that could not be gravity-drained. The work was done safely, with no environmental issues or significant schedule delays.

  9. Infrared spectra of FHF - in alkali halides (United States)

    Chunnilall, C. J.; Sherman, W. F.


    The bifluoride ion, FHF -, has been substitutionally isolated within single crystal samples of several different alkali halides. Infrared spectra of these crystals have been studied for sample temperatures down to 8K when half-bandwidths of less than 1 cm -1 have been observed. (Note that at room temperature ν 3 is observed to have a half-bandwidth of about 40 cm -1). The frequency shifts and half-bandwidth changes caused by cooling are considered together with the frequency shifts caused by pressures up to 10 k bar. The low temperature spectra clearly indicate that FHF - is a linear symmetrical ion when substitutionally isolated within alkali halides of either the NaCl or CsCl structure.

  10. Pyrolysis characteristic of kenaf studied with separated tissues, alkali pulp, and alkali li

    Directory of Open Access Journals (Sweden)

    Yasuo Kojima


    Full Text Available To estimate the potential of kenaf as a new biomass source, analytical pyrolysis was performed using various kenaf tissues, i.e., alkali lignin and alkali pulp. The distribution of the pyrolysis products from the whole kenaf was similar to that obtained from hardwood, with syringol, 4-vinylsyringol, guaiacol, and 4-vinylguaiacol as the major products. The phenols content in the pyrolysate from the kenaf core was higher than that from the kenaf cuticle, reflecting the higher lignin content of the kenaf core. The ratios of the syringyl and guaiacyl compounds in the pyrolysates from the core and cuticle samples were 2.79 and 6.83, respectively. Levoglucosan was the major pyrolysis product obtained from the kenaf alkali pulp, although glycol aldehyde and acetol were also produced in high yields, as previously observed for other cellulosic materials. Moreover, the pathways for the formation of the major pyrolysis products from alkali lignin and alkali pulp were also described, and new pyrolysis pathways for carbohydrates have been proposed herein. The end groups of carbohydrates bearing hemiacetal groups were subjected to ring opening and then they underwent further reactions, including further thermal degradation or ring reclosing. Variation of the ring-closing position resulted in the production of different compounds, such as furans, furanones, and cyclopentenones.

  11. Sulfate Resistance of Alkali Activated Pozzolans


    Bondar, Dali


    The consequence of sulfate attack on geopolymer concrete, made from an alkali activated natural pozzolan (AANP) has been studied in this paper. Changes in the compressive strength, expansion and capillary water absorption of specimens have been investigated combined with phases determination by means of X-ray diffraction. At the end of present investigation which was to evaluate the performance of natural alumina silica based geopolymer concrete in sodium and magnesium sulfate solution, the l...

  12. Effect of Mineral Admixtures on Alkali-Silica Reaction

    Institute of Scientific and Technical Information of China (English)

    ZHANG Chengzhi; WANG Aiqin


    The influence of silica fume,slag and fly ash on alkali-silica reaction under the condition of 70℃ is studied.The results show that silica,slag and fly ash may inhibit alkali-silica reaction only under suitable content.When the content is less than 10%,silica fume does not markedly influence the expansion of alkali-silica reaction.When the content is 15%-20%,silica fume only may delay the expansion of alkali-silica reaction.When the content is 30%-70%,slag may only delay the expansion of alkali-silica reaction,but cannot inhibit the expansion of alkali-silica reaction.When the content is 10%,fly ash does not markedly influence the expansion of alkali-silica reaction.When the content is 20%-30%,fly ash may only delay the expansion of alkali-silica reaction,but cannot inhibit the expansion of alkali-silica reaction.When the content is over 50%,it is possible that fly ash can inhibit effectively alkali-silica reaction.

  13. Ion Pairing in Alkali Nitrate Electrolyte Solutions. (United States)

    Xie, Wen Jun; Zhang, Zhen; Gao, Yi Qin


    In this study, we investigate the thermodynamics of alkali nitrate salt solutions, especially the formation of contact ion pairs between alkali cation and nitrate anion. The ion-pairing propensity shows an order of LiNO3 activity coefficients and suggest that the empirical "law of matching water affinity" is followed by these alkali nitrate salt solutions. The spatial patterns of contact ion pairs are different in the three salt solutions studied here: Li(+) forms the contact ion pair with only one oxygen of the nitrate while Na(+) and K(+) can also be shared by two oxygens of the nitrate. In reproducing the salt activity coefficient using Kirkwood-Buff theory, we find that it is essential to include electronic polarization for Li(+) which has a high charge density. The electronic continuum correction for nonpolarizable force field significantly improves the agreement between the calculated activity coefficients and their experimental values. This approach also improves the performance of the force field on salt solubility. From these two aspects, this study suggests that electronic continuum correction can be a promising approach to force-field development for ions with high charge densities.

  14. Adsorbent Alkali Conditioning for Uranium Adsorption from Seawater. Adsorbent Performance and Technology Cost Evaluation

    Energy Technology Data Exchange (ETDEWEB)

    Tsouris, Costas [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Mayes, Richard T. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Janke, Christopher James [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Dai, Sheng [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Das, S. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Liao, W. -P. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Kuo, Li-Jung [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Wood, Jordana [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Gill, Gary [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Byers, Maggie Flicker [Univ. of Texas, Austin, TX (United States); Schneider, Eric [Univ. of Texas, Austin, TX (United States)


    The Fuel Resources program of the Fuel Cycle Research and Development program of the Office of Nuclear Energy (NE) is focused on identifying and implementing actions to assure that nuclear fuel resources are available in the United States. An immense source of uranium is seawater, which contains an estimated amount of 4.5 billion tonnes of dissolved uranium. This unconventional resource can provide a price cap and ensure centuries of uranium supply for future nuclear energy production. NE initiated a multidisciplinary program with participants from national laboratories, universities, and research institutes to enable technical breakthroughs related to uranium recovery from seawater. The goal is to develop advanced adsorbents to reduce the seawater uranium recovery technology cost and uncertainties. Under this program, Oak Ridge National Laboratory (ORNL) has developed a new amidoxime-based adsorbent of high surface area, which tripled the uranium capacity of leading Japanese adsorbents. Parallel efforts have been focused on the optimization of the physicochemical and operating parameters used during the preparation of the adsorbent for deployment. A set of parameters that need to be optimized are related to the conditioning of the adsorbent with alkali solution, which is necessary prior to adsorbent deployment. Previous work indicated that alkali-conditioning parameters significantly affect the adsorbent performance. Initiated in 2014, this study had as a goal to determine optimal parameters such as base type and concentration, temperature, and duration of conditioning that maximize the uranium adsorption performance of amidoxime functionalized adsorbent, while keeping the cost of uranium production low. After base-treatment at various conditions, samples of adsorbent developed at ORNL were tested in this study with batch simulated seawater solution of 8-ppm uranium concentration, batch seawater spiked with uranium nitrate at 75-100 ppb uranium, and continuous

  15. Role of Calcium Hydroxide in Endodontics: A Review


    Arun A; Sangameshwar Sajjanshetty; Deepak Jain; Saujanya KP; Mohammed Mustafa; Laxmi Uppin; Mahnoor Kadri


    Calcium hydroxide is a multipurpose agent, and there have been an increasing number of indications for its use in endodontics. Some of its indications include inter-appointment intracanal medicaments, endodontic sealers, pulp capping agents, apexification, pulpotomy and weeping canals. The purpose of this article is to review the properties, advantages, disadvantages and various indications for the use of calcium hydroxide in endodontics.


    Institute of Scientific and Technical Information of China (English)


    The fibred mangesiun hydroxide from the bracite was treated with a surface active agent. The modified fibred magesium hydroxide as f lame-retardant,boric acid, barium stearate, polydimethyl siloxane fluid,vinyltr iethoxysilane as synergists of the flame-retardant were added to polyene resin. The flame-resistance polyene material prepared meets the requirements of EWCZ -6287-1.

  17. 21 CFR 872.3250 - Calcium hydroxide cavity liner. (United States)


    ... (CONTINUED) MEDICAL DEVICES DENTAL DEVICES Prosthetic Devices § 872.3250 Calcium hydroxide cavity liner. (a) Identification. A calcium hydroxide cavity liner is a device material intended to be applied to the interior of a prepared cavity before insertion of restorative material, such as amalgam, to protect the pulp of a...

  18. FTIR Analysis of Alkali Activated Slag and Fly Ash Using Deconvolution Techniques (United States)

    Madavarapu, Sateesh Babu

    The studies on aluminosilicate materials to replace traditional construction materials such as ordinary Portland cement (OPC) to reduce the effects caused has been an important research area for the past decades. Many properties like strength have already been studied and the primary focus is to learn about the reaction mechanism and the effect of the parameters on the formed products. The aim of this research was to explore the structural changes and reaction product analysis of geopolymers (Slag & Fly Ash) using Fourier transform infrared spectroscopy (FTIR) and deconvolution techniques. Spectroscopic techniques give valuable information at a molecular level but not all methods are economic and simple. To understand the mechanisms of alkali activated aluminosilicate materials, attenuated total reflectance (ATR) FTIR has been used where the effect of the parameters on the reaction products have been analyzed. To analyze complex systems like geopolymers using FTIR, deconvolution techniques help to obtain the properties of a particular peak attributed to a certain molecular vibration. Time and temperature dependent analysis were done on slag pastes to understand the polymerization of reactive silica in the system with time and temperature variance. For time dependent analysis slag has been activated with sodium and potassium silicates using two different `n'values and three different silica modulus [Ms- (SiO2 /M2 O)] values. The temperature dependent analysis was done by curing the samples at 60°C and 80°C. Similarly fly ash has been studied by activating with alkali hydroxides and alkali silicates. Under the same curing conditions the fly ash samples were evaluated to analyze the effects of added silicates for alkali activation. The peak shifts in the FTIR explains the changes in the structural nature of the matrix and can be identified using the deconvolution technique. A strong correlation is found between the concentrations of silicate monomer in the

  19. Thermalization of different alkali and alkali-earth elements at the TRI{mu}P facility

    Energy Technology Data Exchange (ETDEWEB)

    Shidling, P.D., E-mail: P.Shidling@rug.n [Kernfysisch Versneller Instituut, University of Groningen, Zernikelaan 25, 9747 AA Groningen (Netherlands); Giri, G.S.; Hoek, D.J. van der; Jungmann, K.; Kruithof, W.L.; Onderwater, C.J.G.; Santra, B.; Sohani, M.; Versolato, O.O.; Willmann, L.; Wilschut, H.W. [Kernfysisch Versneller Instituut, University of Groningen, Zernikelaan 25, 9747 AA Groningen (Netherlands)


    Radioactive isotopes produced by the in-flight method are converted into low-energy ions with a thermal ionizer (TI) ion catcher, the operation of which is based on a hot cavity ion source. The extraction efficiency of the TI for different alkali and alkali-earth elements has been studied and compared to a model based on diffusion only. The model describes the stationary limit, i.e. the extraction efficiency, as well as the dynamic response of the TI output when the primary beam is switched on and off.

  20. Low temperature synthesis of Ba1–SrSnO3 ( = 0–1) from molten alkali hydroxide flux

    Indian Academy of Sciences (India)

    B Ramdas; R Vijayaraghavan


    Perovskite structured stannates (Ba1–SrSnO3, = 0.0–1.0) powders have been synthesized for the first time by molten salt synthesis (MSS) method using KOH as the flux at lower temperature (400°C) compared to other methods. The phase formation was confirmed by FT–IR spectroscopy, powder X-ray diffraction (XRD) and the microstructure was analysed by scanning electron microscopy. XRD patterns reveal the formation of single phasic products for parent and substituted products with good crystallinity throughout the range ( = 0.0–1.0). The morphology of the particles of BaSnO3 and SrSnO3 is spherical and rod shaped, respectively. Effect of soaking periods on the grain growth is observed clearly in SrSnO3. Ba0.5Sr0.5SnO3 (BSS5) crystallizes in flake like morphology.

  1. Alkali cation specific adsorption onto fcc(111) transition metal electrodes. (United States)

    Mills, J N; McCrum, I T; Janik, M J


    The presence of alkali cations in electrolyte solutions is known to impact the rate of electrocatalytic reactions, though the mechanism of such impact is not conclusively determined. We use density functional theory (DFT) to examine the specific adsorption of alkali cations to fcc(111) electrode surfaces, as specific adsorption may block catalyst sites or otherwise impact surface catalytic chemistry. Solvation of the cation-metal surface structure was investigated using explicit water models. Computed equilibrium potentials for alkali cation adsorption suggest that alkali and alkaline earth cations will specifically adsorb onto Pt(111) and Pd(111) surfaces in the potential range of hydrogen oxidation and hydrogen evolution catalysis in alkaline solutions.

  2. (abstract) Fundamental Mechanisms of Electrode Kinetics and Alkali Metal Atom Transport at the Alkali Beta'-Alumina/Porous Electrode/Alkali Metal Vapor Three Phase Boundary (United States)

    Williams, R. M.; Jeffries-Nakamura, B.; Ryan, M. A.; Underwood, M. L.; O'Connor, D.; Kisor, A.; Kikkert, S. K.


    The mechanisms of electrode kinetics and mass transport of alkali metal oxidation and alkali metal cation reduction at the solid electrolyte/porous electrode boundary as well as alkali metal transport through porous metal electrodes has important applications in optimizing device performance in alkali metal thermal to electric converter (AMTEC) cells which are high temperature, high current density electrochemical cells. Basic studies of these processes also affords the opportunity to investigate a very basic electrochemical reaction over a wide range of conditions; and a variety of mass transport modes at high temperatures via electrochemical techniques. The temperature range of these investigations covers 700K to 1240K; the alkali metal vapor pressures range from about 10(sup -2) to 10(sup 2) Pa; and electrodes studied have included Mo, W, Mo/Na(sub 2)MoO(sub 4), W/Na(sub 2)WO(sub 4), WPt(sub x), and WRh(sub x) (1.0 alkali metal vapor and alkali metal vapor/solid electrolyte/vapor cells have been used to characterize the reaction and transport processes. We have previously reported evidence of ionic, free molecular flow, and surface transport of sodium in several types of AMTEC electrodes.

  3. Study on fire-retardant nanocrystalline Mg-Al layered double hydroxides synthesized by microwave-crystallization method

    Institute of Scientific and Technical Information of China (English)

    ZHANG Zejiang; XU Chenghua; QIU Fali; MEI Xiujuan; LAN Bin; ZHANG Shuosheng


    Nanocrystalline Mg-Al layered double hydroxides with the particle size being 10-40 nm were firstly prepared by the technology of the microwave-crystallization and the variable-speed addition of the alkali. The obtained samples were characterized by TEM and XRD. The roles of the microwave and addition rate of the alkali were also discussed in the present work. The thermal decomposition activation energy of the nano-LDHs was calculated according to their TG, DTG and DSC curves by the Ozawa method. The results showed that the thermal decomposition of the nano-LDHs had four steps. Thereby the decomposition model of the nano-LDHs was supposed according to the analysis of their thermal decomposition. After PS, ABS, HDPE and PVC were filled with the nano-LDHs, their LOI values could be increased up to 28, 27, 26 and 33, respectively. When the fire-retardant coating contained 1.9% of the nano-LDHs that was 0.27 times the dosage of the conventional TiO2, its fire endurance time reached 32.75min that was 7.05 min longer than that of the best coating containing TiO2 according to the model big-panel combustion test method.

  4. A novel and easy chemical-clock synthesis of nanocrystalline iron-cobalt bearing layered double hydroxides. (United States)

    Hadi, Jebril; Grangeon, Sylvain; Warmont, Fabienne; Seron, Alain; Greneche, Jean-Marc


    A novel synthesis of cobalt-iron layered double hydroxide (LDH) with interlayer chlorides was investigated. The method consists in mixing concentrated solutions of hexaamminecobalt(III) trichloride with ferrous chloride at room temperature and in anoxic conditions. Four initial Fe/Co atomic ratios have been tried out (0.12, 0.6, 1.2 and 1.8). Neither heating nor addition of alkali was employed for adjusting the pH and precipitating the metal hydroxides. Still, each mixture led to the spontaneous precipitation of a LDH-rich solid having a crystal-chemistry that depended on the initial solution Fe/Co. These LDHs phases were carefully characterized by mean of X-ray diffraction, (57)Fe Mössbauer spectrometry, transmission electron microscopy and chemical analysis (total dissolution and phenanthroline method). Solution Eh and pH were also monitored during the synthesis. Increasing initial Fe/Co ratio impacted the dynamic of the observed stepwise reaction and the composition of the resulting product. Once the two solutions are mixed, a spontaneous and abrupt color change occurs after an induction time which depends on the starting Fe/Co ratio. This makes the overall process acting as a chemical clock. This spontaneous generation of CoFe-LDH arises from the interplay between redox chemistries of iron and cobalt-ammonium complexes.

  5. Electrochemical Properties of Nanocomposite Nanoporous Carbon / Nickel Hydroxide

    Directory of Open Access Journals (Sweden)

    O.M. Hemiy


    Full Text Available The electrochemical properties of composite nanoporous carbon / nickel hydroxide as electrode material for hybrid supercapacitors were investigated. Fast reversible faradaic reactions flow was determined in connection with chemical makeup of the -Ni(OH2/С composite. It is shown that increase of nickel hydroxide concentration can intensify reactions. It is found that clean -Ni(OH2 has 238 F/g of specific capacity, but -Ni(OH2/С nanocomposite with 90 % nickel hydroxide has 292 F/g. Such capacity value can be considered as a maximum for these composites.


    Directory of Open Access Journals (Sweden)

    Farhad Zeinaly


    Full Text Available Conventional bleaching of hardwood CMP pulp with magnesium hydroxide (Mg(OH2 show significant benefits over bleaching with sodium hydroxide (NaOH under various conditions. Magnesium hydroxide bleaching generate higher optical properties, higher pulp yield and lower effluent COD at the same chemical charge, but the physical properties were found to be similar for both processes. The initial freeness of the bleached pulps and refining value to reach a target freeness (about 350 ml. CSF were more for the Mg(OH2-based process. The residual peroxide of filtrate from the Mg(OH2-based process was very high as compared to conventional bleaching.

  7. Nickel hydroxide/cobalt-ferrite magnetic nanocatalyst for alcohol oxidation. (United States)

    Bhat, Pooja B; Inam, Fawad; Bhat, Badekai Ramachandra


    A magnetically separable, active nickel hydroxide (Brønsted base) coated nanocobalt ferrite catalyst has been developed for oxidation of alcohols. High surface area was achieved by tuning the particle size with surfactant. The surface area of 120.94 m2 g(-1) has been achieved for the coated nanocobalt ferrite. Improved catalytic activity and selectivity were obtained by synergistic effect of transition metal hydroxide (basic hydroxide) on nanocobalt ferrite. The nanocatalyst oxidizes primary and secondary alcohols efficiently (87%) to corresponding carbonyls in good yields.

  8. Homogeneous Precipitation of Nickel Hydroxide Powders

    Energy Technology Data Exchange (ETDEWEB)

    Bora Mavis


    Precipitation and characterization of nickel hydroxide powders were investigated. A comprehensive precipitation model incorporating the metal ion hydrolysis, complexation and precipitation reactions was developed for the production of the powders with urea precipitation method. Model predictions on Ni{sup 2+} precipitation rate were confirmed with precipitation experiments carried out at 90 C. Experimental data and model predictions were in remarkable agreement. Uncertainty in the solubility product data of nickel hydroxides was found to be the large contributor to the error. There were demonstrable compositional variations across the particle cross-sections and the growth mechanism was determined to be the aggregation of primary crystallites. This implied that there is a change in the intercalate chemistry of the primary crystallites with digestion time. Predicted changes in the concentrations of simple and complex ions in the solution support the proposed mechanism. The comprehensive set of hydrolysis reactions used in the model described above allows the investigation of other systems provided that accurate reaction constants are available. the fact that transition metal ions like Ni{sup 2+} form strong complexes with ammonia presents a challenge in the full recovery of the Ni{sup 2+}. On the other hand, presence of Al{sup 3+} facilitates the complete precipitation of Ni{sup 2+} in about 3 hours of digestion. A challenge in their predictive modeling studies had been the fact that simultaneous incorporation of more than one metal ion necessitates a different approach than just using the equilibrium constants of hydrolysis, complexation and precipitation reactions. Another limitation of using equilibrium constants is that the nucleation stage of digestion, which is controlled mainly by kinetics, is not fully justified. A new program released by IBM Almaden Research Center (Chemical Kinetics Simulator{trademark}, Version 1.01) lets the user change the order of

  9. High-Order Dispersion Coefficients for Alkali-metal Atoms

    Institute of Scientific and Technical Information of China (English)

    KANG Shuai; DING Chi-Kun; CHEN Chang-Yong; WU Xue-Qing


    High-order dispersion coefficients C9,C11,C12,and C13 for the ground-state alkali-metals were calculated by combining the l-dependent model potential of alkali-metal atoms and linear variation method based on B-spline basis functions.The results were compared.

  10. Durability of Alkali Activated Blast Furnace Slag (United States)

    Ellis, K.; Alharbi, N.; Matheu, P. S.; Varela, B.; Hailstone, R.


    The alkali activation of blast furnace slag has the potential to reduce the environmental impact of cementitious materials and to be applied in geographic zones where weather is a factor that negatively affects performance of materials based on Ordinary Portland Cement. The scientific literature provides many examples of alkali activated slag with high compressive strengths; however research into the durability and resistance to aggressive environments is still necessary for applications in harsh weather conditions. In this study two design mixes of blast furnace slag with mine tailings were activated with a potassium based solution. The design mixes were characterized by scanning electron microscopy, BET analysis and compressive strength testing. Freeze-thaw testing up to 100 freeze-thaw cycles was performed in 10% road salt solution. Our findings included compressive strength of up to 100 MPa after 28 days of curing and 120 MPa after freeze-thaw testing. The relationship between pore size, compressive strength, and compressive strength after freeze-thaw was explored.

  11. Laser Spectroscopy of bi-alkali molecules (United States)

    Dutta, Sourav; Altaf, A.; Lorenz, J.; Elliott, D.; Chen, Yong


    We report a study of laser spectroscopy of bi-alkali molecules, such as Li2, Rb2 and LiRb (work is in progress). We have constructed a dual-species (Li/Rb) heat pipe oven with a side viewport. The molecular fluorescence is excited by a dye laser with Rh6G dye (operating between 564 nm and 610 nm) and various home-made diode lasers (operating near 635 nm and 665 nm). The fluorescence is recorded using a .5ex1 -.1em/ -.15em.25ex4 m monochromator with a 0.1 nm (˜ 3 cm-1) spectral resolution. Transitions to the X^1σg^+ in Li2 and Rb2 have been measured and studies on LiRb are in progress. Molecular parameters, such as force constant, may be obtained from the analysis of the data (which agree with previously known values to within ˜ 3%). Using the known values of dissociation energy De and harmonic frequency φe for the alkali dimers, we also demonstrate that simple calculations with Morse potential approximation can be used to estimate the molecular transition wavelengths to within a few (1-3) nanometers from the experimentally measured values. Such information will aid in creating cold molecules via photoassociation in a dual species magneto-optical trap (LiRb in our case).

  12. Pathways of birnessite formation in alkali medium

    Institute of Scientific and Technical Information of China (English)

    FENG Xionghan; TAN Wenfeng; LIU Fan; HUANG Qiaoyun; LIU Xiangwen


    Birnessite is a common weathering and oxidation product of manganese-bearing rocks. An O2 oxidation procedure of Mn(OH)2 in the alkali medium has been used to synthesize birnessite. Fast and powder X-ray diffraction (XRD), transmission electron microscopy (TEM), electron diffraction (ED), energy dispersed X-ray analysis (EDAX), infrared spectroscopy (IR) techniques and chemical composition analysis, Eh-pH equilibrium diagram approaches were employed to investigate the reaction process and pathways of birnessite formation. Results showed that the process of the birnessite formation could be divided into four stages: (1) formation stage for hausmannite and feitknechtite, (2) stage of transformation of hausmannite and feitknechtite to buserite, (3) buserite crystal growing stage, and (4) stage of conversion of buserite into birnessite. Mn(OH)2 was mainly present as amorphous state only for a short initial time of oxidation reaction. In the oxidation process, buserite formed following two pathways by recrystallization after dissolution of the intermediates, and the transformations of the minerals depended on the Eh determined by the dissolved O2 concentration on their surfaces. The results are fundamental in further exploration on the mechanism of birnessite formation in the alkali medium. A great practical significance would also be expected with respect to the areas of material sciences.

  13. Alkali-based pretreatments distinctively extract lignin and pectin for enhancing biomass saccharification by altering cellulose features in sugar-rich Jerusalem artichoke stem. (United States)

    Li, Meng; Wang, Jun; Yang, Yuezhou; Xie, Guanghui


    Jerusalem artichoke (JA) has been known as a potential nonfood feedstock for biofuels. Based on systems analysis of total 59 accessions, both soluble sugar and ash could positively affect biomass digestibility after dilute sodium hydroxide pretreatment (A). In this study, one representative accession (HEN-3) was used to illustrate its enzymatic digestibility with pretreatments of ultrasonic-assisted dilute sodium hydroxide (B), alkaline peroxide (C), and ultrasonic-assisted alkaline peroxide (D). Pretreatment D exhibited the highest hexose release rate (79.4%) and total sugar yield (10.4 g/L), which were 2.4 and 2.6 times higher, respectively, than those of the control. The analysis of cellulose crystalline index (CrI), cellulose degree of polymerization (DP), thermal behavior and SEM suggested that alkali-based pretreatments could distinctively extract lignin and pectin polymers, leading to significant alterations of cellulose CrI and DP for high biomass saccharification. Additionally, hydrogen peroxide (H2O2) could significant reduce the generation of fermentation inhibitors during alkali-based pretreatments.

  14. 铝酸钡与氢氧化钡脱硫过程比较%Comparison of Barium Aluminate and Barium Hydroxide Desulfurization Process

    Institute of Scientific and Technical Information of China (English)

    张念炳; 黎志英; 丁彤


    The seed precipitation liquor was desulfurized with barium aluminate and barium hydroxide respectively. The desulfurization slag was characterized by XRD analysis, and the desulfurization process was compared. The results show that barium hydroxide exceeds barium aluminate with better desulfurization in terms of effect, speed and duration. In the desulfurization process with barium aluminate, 2BaO · Al2O3 · 5H2O is firstly produced in the reaction of barium aluminate with alkali, and then it reacts with sodium sulfate and sodium carbonate. To compare, Ba(OH)2 · 8H2O directly reacts with sodium sulfate and sodium carbonate in the desulfurization process with barium hydroxide. Both of desulfurization reaction processes can be described with "shrinking core model".%用铝酸钡和氢氧化钡对种分母液进行脱硫试验,对脱硫渣进行XRD分析,并比较脱硫过程.结果表明,氢氧化钡的脱硫效果更好,脱硫完成时间更短,速率更快;铝酸钡先与碱液反应生成2BaO·Al2O3·5H2O,再与硫碱和碳碱反应,而氢氧化钡直接与硫碱和碳碱反应,脱硫过程均可用未反应核模型描述.


    Institute of Scientific and Technical Information of China (English)

    SonglinWang; WenxiaLiu


    Layered double hydroxides consisting of layers withcationic charges may be potential candidates ofcationic microparticles forming synergetic retentioneffect with anionic polyacrylamide. In this work, thelayered double hydroxides with various molar ratiosof Mg/AI were synthesized by co-precipitation ofmagnesium chloride and aluminum chloride and pep-tized by intense washing with water. The chemicalformula, particle size, Zeta potential of the layereddouble hydroxide were analyzed. It was found thatpositively charged magnesium aluminum hydroxidewith particle diameter in nanoparticle size could beprepared. The Zeta potential and particle size varywith the feed molar ratio of Mg/A1 and the peptizingprocess, respectively. The Zeta potential is also pHdependent. The retention experiments carried out onDDJ show that when used together with anionic poly-acrylamide, the positively charged colloidal doublehydroxide greatly improves the retention of reedpulps. The chemical formula, particle size and Zetapotential of the colloidal double hydroxide all affectits retention behavior.

  16. Tertiary dentinogenesis with calcium hydroxide: a review of proposed mechanisms. (United States)

    Sangwan, P; Sangwan, A; Duhan, J; Rohilla, A


    Calcium hydroxide has been used extensively in dentistry for a century. Despite its widespread use as a pulp-capping agent, its mechanisms of action still remain ambiguous. Understanding its modes of action will lead to a broader understanding of the mechanisms associated with induced dentinogenesis and help in optimizing the currently available agents to target specific regenerative processes to obtain the best possible clinical outcomes. A literature search relating to mechanisms of dentinogenesis of calcium hydroxide up to December 2011 was carried out using pubmed and MEDLINE database searches as well as manual searching of cross-references from identified studies. Resulting suggestions regarding dentinogenic mechanisms of calcium hydroxide range from direct irritating action of the material to induction of release of biologically active molecules. The purpose of this article is to discuss various mechanisms through which calcium hydroxide may induce tertiary dentinogenesis in the light of observations made in included studies.

  17. Hydrothermal synthesis of lanthanide (hydr)oxide micro/nanorods in presence of tetrabutylammonium hydroxide

    Institute of Scientific and Technical Information of China (English)

    李银艳; 徐时清


    Uniform and well-defined lanthanide hydroxide and oxide micro/nanorods Ln(OH)3(Ln=La, Pr, Sm, Eu, Gd, Er) and Gd(OH)3:Eu3+, Gd2O3:Eu3+ were successfully synthesized through a green and facile hydrothermal method. Tetrabutylammonium hydroxide (TBAH) and lanthanide nitrides were used as the hydrothermal precursors without the addition of any templates/surfactants. The products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM) and photoluminescence (PL) spectra. The result demonstrated that lanthanide hydroxide micro/nanorods with 20–80 nm in diameter and 50–450 in length were obtained. The size of the Ln(OH)3 (Ln=La, Pr, Sm, Eu, Gd, Er) rods increased with the increase of the atomic number. The size of the Gd(OH)3:Eu3+ rods decreased with the increase of pH value by modulating the amount of the TBAH solution. The as-formed product via the hydrothermal process, Gd(OH)3:Eu3+, could be transformed to Gd2O3:Eu3+ with the same morphology and a slight shrinking in size after a post annealing process. It is a facial method to synthesize photoluminescent nanomaterial of Gd2O3:Eu3+. The Gd2O3:Eu3+ microrods exhibited strong red emission corresponding to5D0→7F2 transition (610 nm) of Eu3+ under UV light excitation (257 nm).

  18. IRMPD Action Spectroscopy of Alkali Metal Cation-Cytosine Complexes: Effects of Alkali Metal Cation Size on Gas Phase Conformation

    NARCIS (Netherlands)

    Yang, B.; Wu, R.R.; Polfer, N.C.; Berden, G.; Oomens, J.; Rodgers, M.T.


    The gas-phase structures of alkali metal cation-cytosine complexes generated by electrospray ionization are probed via infrared multiple photon dissociation (IRMPD) action spectroscopy and theoretical calculations. IRMPD action spectra of five alkali metal cation-cytosine complexes exhibit both simi

  19. Role of Calcium Hydroxide in Endodontics: A Review

    Directory of Open Access Journals (Sweden)

    Arun A


    Full Text Available Calcium hydroxide is a multipurpose agent, and there have been an increasing number of indications for its use in endodontics. Some of its indications include inter-appointment intracanal medicaments, endodontic sealers, pulp capping agents, apexification, pulpotomy and weeping canals. The purpose of this article is to review the properties, advantages, disadvantages and various indications for the use of calcium hydroxide in endodontics.

  20. Structure and properties of porous ceramics obtained from aluminum hydroxide


    Levkov, R.; Kulkov, Sergey Nikolaevich


    In this paper the study of porous ceramics obtained from aluminum hydroxide with gibbsite modification is presented. The dependence of porosity and mechanical characteristics of the material sintered at different temperatures was studied. It was shown that compressive strength of alumina ceramics increases by 40 times with decreasing the pore volume from 65 to 15%. It was shown that aluminum hydroxide may be used for pore formation and pore volume in the sintered ceramics can be controlled by...


    Institute of Scientific and Technical Information of China (English)

    Songlin Wang; Wenxia Liu


    Layered double hydroxides consisting of layers with cationic charges may be potential candidates of cationic microparticles forming synergetic retention effect with anionic polyacrylamide. In this work, the layered double hydroxides with various molar ratios of Mg/Al were synthesized by co-precipitation of magnesium chloride and aluminum chloride and peptized by intense washing with water. The chemical formula, particle size, Zeta potential of the layered double hydroxide were analyzed. It was found that positively charged magnesium aluminum hydroxide with particle diameter in nanoparticle size could be prepared. The Zeta potential and particle size vary with the feed molar ratio of Mg/Al and the peptizing process, respectively. The Zeta potential is also pH dependent. The retention experiments carried out on DDJ show that when used together with anionic polyacrylamide, the positively charged colloidal double hydroxide greatly improves the retention of reed pulps. The chemical formula, particle size and Zeta potential of the colloidal double hydroxide all affect its retention behavior.

  2. Application of high throughput pretreatment and co-hydrolysis system to thermochemical pretreatment. Part 2: Dilute alkali. (United States)

    Li, Hongjia; Gao, Xiadi; Demartini, Jaclyn D; Kumar, Rajeev; Wyman, Charles E


    High throughput pretreatment (HTPH) and enzymatic hydrolysis systems are now vital for screening large numbers of biomass samples to investigate biomass recalcitrance over various pretreatment and enzymatic hydrolysis conditions. Although hydrothermal pretreatment is currently being employed in most high throughput applications, thermochemical pretreatment at low and high pH conditions can offer additional insights to better understand the roles of hemicellulose and lignin, respectively, in defining biomass recalcitrance. Thus, after successfully applying the HTPH approach to dilute acid pretreatment [Gao et al. (2012) Biotechnol. Bioeng. 110(3): 754-762], extension to dilute alkali pretreatment was also achieved using a similar single-step neutralization and buffering concept. In the latter approach, poplar and switchgrass were pretreated with 1 wt% sodium hydroxide at 120°C for different reaction times. Following pretreatment, an H₂Cit⁻/HCit²⁻ buffer with a pH of 4.5 was used to condition the pretreatment slurry to a pH range of 4.69-4.89, followed by enzymatic hydrolysis for 72 h of the entire mixture. Sugar yields showed different trends for poplar and switchgrass with increases in pretreatment times, demonstrating the method provided a clearly discernible screening tool at alkali conditions. This method was then applied to selected Populus tremuloides samples to follow ring-by-ring sugar release patterns. Observed variations were compared to results from hydrothermal pretreatments, providing new insights in understanding the influence of biomass structural differences on recalcitrance.

  3. Ageing behaviour of unary hydroxides in trivalent metal salt solutions: Formation of layered double hydroxide (LDH)-like phases

    Indian Academy of Sciences (India)

    Michael Rajamathi; P Vishnu Kamath


    The hydroxides of Mg, Ni, Cu and Zn transform into layered double hydroxide (LDH)-like phases on ageing in solutions of Al or Cr salts. This reaction is similar to acid leaching and proceeds by a dissolution–reprecipitation mechanism offering a simple method of LDH synthesis, with implications for the accepted theories of formation of LDH minerals in the earth’s crust.

  4. The Effects of Aluminium Hydroxide and Magnesium Hydroxide on the Mechanical Properties of Thermoplastic Polyurethane Materials

    Directory of Open Access Journals (Sweden)

    Erkin Akdoğan


    Full Text Available Thermoplastic polyurethane materials are widely used in automotive, clothing, electrical and electronics, medical, construction, machine industry due to excellent physical and chemical properties. Thermoplastic polyurethane materials combustion and resistance to high temperature characteristics are poor. Additives and fillers are added into the polyurethane matrix to improve those properties. Particularly adding these agents as a flame retardant are affect mechanical properties of polyurethane materials. Therefore, it is important to determinate the mechanical properties of these materials. In this study, 5% by weight of the thermoplastic polyurethane material, aluminium tri hydroxide (ATH, (Al2O3 3H2O and magnesium hydroxide (MgOH, (Mg(OH2 were added. Ammonium polyphosphate (APP as an intumescent flame retardant with inorganic flame retardants were added to increase the flame resistance of produced composite structure. Tensile test, tear test, hardness and Izod impact tests were made and compared of those produced composites. As a result of experiments the addition of ATH has lowered the tensile strength and tear strength contrast to this the addition of MgOH has improved those properties. Hardness and Izod impact test results were showed that both of the additives have no negative effect.

  5. Thermoluminescence of alkali halides and its implications

    Energy Technology Data Exchange (ETDEWEB)

    Gartia, R.K., E-mail: [Physics Department, Manipur University, Imphal 795003 (India); Rey, L. [Aerial-CRT-parc d' Innovation, B.P. 40443, F-67412 Illkirch Cedex (France); Tejkumar Singh, Th. [Physics Department, Manipur University, Imphal 795003 (India); Basanta Singh, Th. [Luminescence Dating Laboratory, Manipur University, Imphal 795003 (India)


    Trapping levels present in some alkali halides namely NaCl, KCl, KBr, and KI are determined by deconvolution of the thermoluminescence (TL) curves. Unlike most of the studies undertaken over the last few decades, we have presented a comprehensive picture of the phenomenon of TL as an analytical technique capable of revealing the position of the trapping levels present in the materials. We show that for all practical purposes, TL can be described involving only the three key trapping parameters, namely, the activation energy (E), the frequency factor (s), and the order of kinetics (b) even for complex glow curves having a number of TL peaks. Finally, based on these, we logically infer the importance of TL in development and characterization of materials used in dosimetry, dating and scintillation.

  6. Ambient Cured Alkali Activated Flyash Masonry Units (United States)

    Venugopal, K.; Radhakrishna; Sasalatti, Vinod M.


    Geopolymers belong to a category of non-conventional and non-Portland cement based cementitious binders which are produced using industrial by products like fly ash and ground granulated blast furnace slag (GGBFS). This paper reports on the development of geopolymer mortars for production of masonry units. The geopolymer mortars were prepared by mixing various by products with manufactured sand and a liquid mixture of sodium silicate and sodium hydroxide solutions. After curing at ambient conditions, the masonry units were tested for strength properties such as water absorption, initial rate of absorption, compression, shear- bond, and stress-strain behaviour etc. It was observed that the flexural strength of the blocks is more than 2 MPa and shear bond strength is more than 0.4MPa. It was found that the properties of geopolymer blocks were superior to the traditional masonry units. Hence they can be recommended for structural masonry.

  7. Acid and Alkali Buffer Capacity of Typical Fluvor-Aquic Soil in Huang-HuaiHai Plain

    Institute of Scientific and Technical Information of China (English)

    HUANG Ping; ZHANG Jia-bao; ZHU An-ning; ZHANG Cong-zhi


    Soil acid and alkali buffer capacity, as a major indicator for evaluating its vulnerability and resistibility to acidification and alkalization, is an important factor affecting the sustainable agriculture, through knowledge on which soil acidification process can be predicted and modified. In this study, titration curve method was adopted to investigate the pH buffer capacity (pHBC) of fluvor-aquic soil, and separate titration curves were established by adding incremental amounts of either standardized hydrochloric acid (HCl) (0.12 mol L-1) or sodium hydroxide (NaOH) (0.10 mol L-1) to soil suspended in deionized water (soil:solution=1:5). Soil pH was measured after 7 d resuspension and isothermal equilibrium (T= 25℃). Linear regressions were fitted to the linear portion of each titration curve and the slopes of these lines were derived as the soil pHBC. The results showed that significant correlations between the amounts of adding acid or alkali and each pH change were presented, and titration curve method was feasible for measurement of pHBC on typical fluvor-aquic soil in Huang-Huai-Hai Plain, and the coefficients of determination were higher than the similar researches on acid soil (R2= 0.96). The slope-derived pHBC of acid and alkali were 158.71 and 25.02 mmol kg-1, respectively. According to the classification of soil buffer systems, the soil tested belongs to the calcium carbonate buffer system, carbonates contribute the most to pHBC, and the contribution of soil organic matter relatively less than it.

  8. Alkali-activated cementitious materials: Mechanisms, microstructure and properties (United States)

    Jiang, Weimin

    The goal of this study was to examine the activation reaction, microstructure, properties, identify the mechanisms of activation, and achieve an enhanced understanding of activation processes occurring during the synthesis of alkali activated cementitious materials (AAC). The discussions classify the following categories. (1) alkali activated slag cement; (2) alkali activated portland-slag cement; (3) alkali activated fly ash-slag cement; (4) alkali activated pozzolana-lime cement; (5) alkali activated pozzolana cement. The activators involved are NaOH, KOH; Nasb2SOsb4;\\ Nasb2COsb3;\\ CaSOsb4, and soluble silicate of sodium and potassium. The effect of alkali activation on the microstructure of these materials were analyzed at the micro-nanometer scale by SEM, EDS, ESEM, and TEM. Also sp{29}Si and sp{27}Al MAS-NMR, IR, Raman, TGA, and DTA were performed to characterize the phase in these systems. Slag, fly ash, silica fume, as well as blended cements containing mixtures of these and other components were characterized. A set of ordinary portland cement paste samples served as a control. This study confirmed that AAC materials have great potential because they could generate very early high strength, greater durability and high performance. Among the benefits to be derived from this research is a better understanding of the factors that control concrete properties when using AAC materials, and by controlling the chemistry and processing to produce desired microstructures and properties, as well as their durability.

  9. Controlled in-situ dissolution of an alkali metal

    Energy Technology Data Exchange (ETDEWEB)

    Jones, Jeffrey Donald; Dooley, Kirk John; Tolman, David Donald


    A method for the controllable dissolution of one or more alkali metals from a vessel containing a one or more alkali metals and/or one or more partially passivated alkali metals. The vessel preferably comprising a sodium, NaK or other alkali metal-cooled nuclear reactor that has been used. The alkali metal, preferably sodium, potassium or a combination thereof, in the vessel is exposed to a treatment liquid, preferably an acidic liquid, more preferably citric acid. Preferably, the treatment liquid is maintained in continuous motion relative to any surface of unreacted alkali metal with which the treatment liquid is in contact. The treatment liquid is preferably pumped into the vessel containing the one or more alkali metals and the resulting fluid is extracted and optionally further processed. Preferably, the resulting off-gases are processed by an off-gas treatment system and the resulting liquids are processed by a liquid disposal system. In one preferred embodiment, an inert gas is pumped into the vessel along with the treatment liquid.

  10. Influence of alkalis from different sources than cement in the evolution of alkali-silica reaction

    Directory of Open Access Journals (Sweden)

    Olague, C.


    Full Text Available A bibliographical revision of the existent literature allows showing symptoms of alkali-silica reaction (ASR in highways, and the practical and economic method uranyl acetate to confirm the presence of ASR. The existence of reaction in concrete pavements of Chihuahua City was verified by a visual observation of patterns cracks, examination of gel deposits and the presence of reactive materials. Considering that the cement used to construct this pavements with problems of ASR, was low alkalis cement, the research was devoted to study the influence of alkalis coming from different sources than cement in the evolution of reaction such as: a aggregates: gravel and sand, b mix water, c additives and d minerals additions The initial classification of cements like high and low alkalis concerned to ASR must be revised for accept the fact that there is not a unique maximum limit alkalis of cement under which the expansible reactivity cannot occur.

    Una revisión bibliográfica de la literatura existente permite mostrar las manifestaciones de reacción álcali-sílice (RAS en estructuras de carreteras y el método práctico y económico de acetato de uranilo para confirmar la presencia de RAS. La existencia de la reacción en pavimentos de hormigón de la ciudad de Chihuahua se pudo confirmar tras la observación visual de modelos de grietas, estudios de depósitos de gel y existencia de fuentes de materiales reactivos. Considerando que el cemento utilizado para construir los tramos de pavimento con problemas de RAS, era un cemento bajo en álcalis, se enfocó la investigación al estudio de la influencia de los álcalis provenientes de fuentes distintas al cemento en la evolución de la reacción tales como: a áridos gruesos y finos, b agua de mezclado, c aditivos y d adiciones minerales El concepto inicial de clasificación de cementos altos y bajos en álcalis con respecto a la RAS debe ser revisado para aceptar el hecho de que no hay un solo

  11. Pi resonance of chemisorbed alkali atoms on noble metals. (United States)

    Borisov, A G; Sametoglu, V; Winkelmann, A; Kubo, A; Pontius, N; Zhao, J; Silkin, V M; Gauyacq, J P; Chulkov, E V; Echenique, P M; Petek, H


    We have performed a joint experimental and theoretical study of the unoccupied electronic structure of alkali adsorbates on the (111) surfaces of Cu and Ag. Combining angle- and time-resolved two-photon photoemission spectroscopy with wave packet propagation calculations we show that, along with the well known sigma resonance oriented along the surface normal, there exist long-lived alkali-localized resonances oriented parallel to the surface (pi symmetry). These new resonances are stabilized by the projected band gap of the substrate and emerge primarily from the mixing of the p and d Rydberg orbitals of the free alkali atom modified by the interaction with the surface.

  12. Important role of alkali atoms in A4C60


    Gunnarsson, O.; Erwin, S. C.; Koch, E.; Martin, R. M.


    We show that hopping via the alkali atoms plays an important role for the t1u band of A4C60 (A=K, Rb), in strong contrast to A3C60. Thus the t1u band is broadened by more than 40 % by the presence of the alkali atoms. The difference between A4C60 and A3C60 is in particular due to the less symmetric location of the alkali atoms in A4C60.

  13. Influence of Alkali Treatment on the Surface Area of Aluminium Dross

    Directory of Open Access Journals (Sweden)

    N. S. Ahmad Zauzi


    Full Text Available Aluminium dross is an industrial waste from aluminium refining industry and classified as toxic substances. However, the disposal of dross as a waste is a burden to aluminium manufacturer industries due to its negative effects to the ecosystem, surface, and ground water. Therefore the purpose of this study is to evaluate the influence of sodium hydroxide (NaOH on the surface area and pore size of aluminium dross. There were 3 stages in the treatment activities, which were leaching, precipitation, and calcination process. The optimum result from this study was the surface area of aluminium dross increases from 10.1 m2/g up to 80.0 m2/g at 40°C, 1% NaOH, and 15-minute reaction time. Thus, aluminium dross has a potential to be converted into other useful material such as catalyst and absorbent. The benefit of this research is that the hazardous industrial waste can be turned into wealth to be used in other applications such as in catalytic activities and absorber in waste water treatment. Further investigation on the physicochemical of aluminium dross with different acid or alkali should be conducted to get deeper understanding on the aluminium dross as a catalyst-type material.


    Directory of Open Access Journals (Sweden)

    H. A. Abdel-Gawwad


    Full Text Available The effect of different proportions and different reactivities of MgO on the drying shrinkage and compressive strength of alkali activated slag pastes (AAS has been investigated. The slag was activated by 6 wt.% sodium hydroxide and liquid sodium silicate at ratio of 3:3 (wt.. The different reactivities of MgOs were produced from the calcination of hydromagnesite at different temperatures (550, 1000, 1250 C. The results showed that the reactivity of magnesium oxide decreases with increasing the calcination temperature. Also, the drying shrinkage of AAS was reduced by the replacement of slag with MgOs. The highly reactive MgO accelerated the hydration of AAS at early ages. The replacement of slag with 5% MgO550 increased one day compressive strength by ~26 % while MgO1250 had little effect. A significant increase in strength was observed after 7 days in case of replacement of slag with 5 % MgO1250. The MgO reacts with slag to form hydrotalcite likephases (Ht as detected by XRD, FTIR spectroscopy, TGA/DTG analysis and SEM.

  15. Combined alkali and acid pretreatment of spent mushroom substrate for reducing sugar and biofertilizer production. (United States)

    Zhu, Hong-Ji; Liu, Jia-Heng; Sun, Li-Fan; Hu, Zong-Fu; Qiao, Jian-Jun


    Spent mushroom substrate (SMS) was pretreated with alkaline reagents including potassium hydroxide, lime and ammonia to enhance enzymatic saccharification. Under the best pretreatment conditions (1M KOH, 80 °C, 90 min; 1M lime, 80 °C, 120 min; 10 M ammonia, 70 °C, 120 min), the total reducing sugar (TRS) yield reached 258.6, 204.2 and 251.2 mg/g raw SMS, which were respectively 6.15, 4.86, and 5.98 times of untreated SMS. The effects of pretreatment by above alkaline reagents and sulfuric acid on the composition and structure of SMS were evaluated to provide comparative performance data. A new process, combined alkali and acid (CAA) pretreatment followed by enzymatic hydrolysis, was innovatively proposed to improve the cost-effectiveness and avoid environmental problems. The SMS residue after CAA pretreatment-enzymatic hydrolysis process was converted to biofertilizer with Pichia farinose FL7 and a cell density of 3.0×10(8) cfu/g in biomass was attained.

  16. Experimental Study on Full-Scale Beams Made by Reinforced Alkali Activated Concrete Undergoing Flexure

    Directory of Open Access Journals (Sweden)

    Linda Monfardini


    Full Text Available Alkali Activated Concrete (AAC is an alternative kind of concrete that uses fly ash as a total replacement of Portland cement. Fly ash combined with alkaline solution and cured at high temperature reacts to form a binder. Four point bending tests on two full scale beams made with AAC are described in this paper. Companion small material specimens were also casted with the aim of properly characterizing this new tailored material. The beam’s length was 5000 mm and the cross section was 200 mm × 300 mm. The AAC consisted of fly ash, water, sand 0–4 mm and coarse aggregate 6–10 mm; and the alkaline solution consisted of sodium hydroxide mixed with sodium silicate. No cement was utilized. The maximum aggregate size was 10 mm; fly ash was type F, containing a maximum calcium content of 2%. After a rest period of two days, the beam was cured at 60 °C for 24 h. Data collected and critically discussed included beam deflection, crack patterns, compressive and flexural strength and elastic modulus. Results show how AAC behavior is comparable with Ordinary Portland Cement (OPC based materials. Nonlinear numerical analyses are finally reported, promoting a better understanding of the structural response.

  17. Studying the effect of thermal and acid exposure on alkali activated slag Geopolymer

    Directory of Open Access Journals (Sweden)

    Khater H.M.


    Full Text Available This article reports a study about thermal stability as well as acid resistance of geopolymer materials prepared from Ground Granulated Blast Furnace Slag (GGBFS, Air Cooled Slag (ACS, Silica fume (SF and cement kiln dust (CKD using 6% (weight of equal mix from alkaline sodium hydroxide and sodium silicate activators. Study of addition of ACS, SF and CKD as partial replacement of GGBFS is investigated so as to improve the mechanical and microstructural properties of geopolymer mixes. Compressive strength and SEM were utilized in these studies. Materials were prepared using water/binder of 0.30 at 38°C and 100% RH. Results showed that geopolymer materials prepared using alkali activated slag exhibit large changes in compressive strength with increasing the firing temperature from 300 to 1000°C and exhibit an enhancement in thermal stability as compared to concrete specimens. Materials prepared by replacing GGBFS by 15% ACS resist thermal deterioration up to 1000°C. It was suggested to be suitable for refractory insulation applications as well as for production of nuclear concrete reactors. On the other hand, geopolymer mixes exhibit low stability upon subjecting to different concentration from the mix of nitric and hydrochloric acid in equal ratio (1:1. Current studies of geopolymer microstructure were focused on the morphology as well as the relationship between compositions and mechanical properties.

  18. Bioethanol Production from Paper Fibre Residue Using Diluted Alkali Hydrolysis and the Fermentation Process

    Directory of Open Access Journals (Sweden)

    G. Sathya Geetha


    Full Text Available The state of art for the bioethanol production from paper fibre residue using diluted alkali hydrolysis and fermentation processes was evaluated. Hydrolysis of paper fibre residue with diluted sodium hydroxide at various time period, temperature and concentration were investigated. The paper fibre residue was pre-steamed, impregnated with diluted NaOH (0 to 25% and subsequently hydrolyzed in a reactor at temperatures that ranged between 30 to 50 oC, for reaction time between 30 minutes to 150 minutes. The highest yield of monosaccharide (indicating the efficient hydrolysis of cellulose and hemi cellulose was found at a temperature of 35 oC for a reaction time of 90 minutes. Fermentability of hemicelluloses hydrolysate was tested using monosaccharide fermenting microorganism Penicillium chrysogenum and Saccharomyces cereviacea. The fermentability of the hydrolysate decreased strongly for hydrolysate produced at temperature higher than 50 oC. The ethanol concentration of monosaccharide hydrolysate was found to be 34.06 g/L and the ethanol yield was 0.097 g/g.

  19. The citotoxicity of calcium hydroxide intracanal dressing by MTT assay

    Directory of Open Access Journals (Sweden)

    Nanik Zubaidah


    Full Text Available Calcium hydroxide had been used as the intracanal dressing in endodontic treatment due to its high alkaline and high antimicrobial capacity. It also be able to dissolve the necrotic tissue, prevent the root resorbtion and regenerate a new hard tissue. The aim of this study is to identify the concentration of calcium hydroxide that has the lowest citotoxicity. There are 5 groups, each group had 8 samples with different concentration of calcium hydroxide. Group I: 50%, Group II: 55%, Group III: 60%, Group IV: 65% and Group V: 70%. The citotoxicity test by using enzymatic assay of MTT [3-(4.5- dimethylthiazol-2yl ]-2.5 diphenyl tetrazolium bromide, against fibroblast cell (BHK-21. The result of susceptibility test was showed by the citotoxicity detection of the survive cell of fibroblast that was measured spectrophotometrically using 595 nm beam. The data was analyzed using One-Way ANOVA test with significant difference α = 0.05 and subsequently LSD test. The result showed that in concentration 50%, 55%, 60%, 65%, and 70% calcium hydroxide had low toxicity, but calcium hydroxide 60%, had the lowest toxicity.

  20. Photo-oxidation of EPDM/layered double hydroxides composites: Influence of layered hydroxides and stabilizers

    Directory of Open Access Journals (Sweden)


    Full Text Available The photo-oxidation of ethylene propylene diene monomer (EPDM/ layered double hydroxide (LDH composites as well as EPDM/LDH with stabilizers is studied under accelerated UV irradiation (λ≥290 nm at 60°C for different time intervals. The development of functional groups during oxidation was monitored by FT-IR spectroscopy. The photodegradation of the pristine polymer and composites take place and the increase in hydroxyl and carbonyl groups with irradiation times, was estimated. EPDM filled LDH showed higher degradation rate than pristine EPDM, while in acidic medium EPDM/LDH showed almost equal degradation as in isolated conditions. These results show the advantages of LDHs as a filler as well as an acid killer. The effect of stabilizers is very less because of their concentration in comparison of LDH.

  1. Structure and electronic properties of alkali-C60 nanoclusters. (United States)

    Rabilloud, Franck


    I investigated the structural and electronic properties of both Na(n)C(60) and Li(n)C(60) (n alkali atoms over the C(60) surface is analyzed. The hypotheses for either an homogeneous coating of the C(60) surface by the alkali atoms or the growth of an alkali droplet not wetting the fullerene surface are discussed. Lithium atoms are found to coat homogeneously the fullerene on the C(60) surface via pentagonal sites, contrary to sodium atoms, which prefer to form 4-atom islands on the surface. The charge transfer, the energetics, and the dipole moments are discussed in relation with available results. The adsorption of alkali atoms on the C(60) surface considerably enhances the capacity of C(60) to accept electrons. The arrangement of lithium atoms seems more favorable for the hydrogen storage than that of sodium atoms.

  2. Hall Determination of Atomic Radii of Alkali Metals (United States)

    Houari, Ahmed


    I will propose here an alternative method for determining atomic radii of alkali metals based on the Hall measurements of their free electron densities and the knowledge of their crystal structure. (Contains 2 figures.)

  3. Electric field-induced softening of alkali silicate glasses

    Energy Technology Data Exchange (ETDEWEB)

    McLaren, C.; Heffner, W.; Jain, H. [Department of Materials Science and Engineering, Lehigh University, Bethlehem, Pennsylvania 18015 (United States); Tessarollo, R.; Raj, R. [Department of Mechanical Engineering, University of Colorado at Boulder, Boulder, Colorado 80309 (United States)


    Motivated by the advantages of two-electrode flash sintering over normal sintering, we have investigated the effect of an external electric field on the viscosity of glass. The results show remarkable electric field-induced softening (EFIS), as application of DC field significantly lowers the softening temperature of glass. To establish the origin of EFIS, the effect is compared for single vs. mixed-alkali silicate glasses with fixed mole percentage of the alkali ions such that the mobility of alkali ions is greatly reduced while the basic network structure does not change much. The sodium silicate and lithium-sodium mixed alkali silicate glasses were tested mechanically in situ under compression in external electric field ranging from 0 to 250 V/cm in specially designed equipment. A comparison of data for different compositions indicates a complex mechanical response, which is observed as field-induced viscous flow due to a combination of Joule heating, electrolysis and dielectric breakdown.

  4. A Novel Eco-Alkali Chemistry in Newspaper Flotation Deinking

    Directory of Open Access Journals (Sweden)

    Ivana Plazonic


    Full Text Available Performance and efficiency of fresh offset-printed daily Croatian newspaper deinked by novel chemistry, named Eco-alkali, were investigated in this study. Eco-alkali is naturally gained alkali prepared from domestic by-product wood fly ash collected after hardwood ignition. Brightness, opacity and effective residual ink concentration (ERIC as optical properties were evaluated for the deinked pulp before and after flotation. Lingering ink particles and their total surface area were measured by image analysis method. Experimental results are compared to the pulp deinked with worldwide accepted method INGEDE Method 11 using identical steps through the whole deinking process. The findings obtained from present work, especially removing particle efficiency results before flotation, indicated that eco-alkali have potential to be used in flotation deinking of newspapers.

  5. Acid/alkali gated photochromism of two diarylperfluorocyclopentenes

    Institute of Scientific and Technical Information of China (English)

    CHEN; ZiHui; ZHAO; ShengMin; LI; ZhongYu; ZHANG; Zhi; ZHANG; FuShi


    Two novel diarylfuorocyclopentenes, which underwent gated photochromism, were synthesized. It was found that the photochromic property of these diarylethenes could be switched by alternative addition of acids/alkalis, which could provide a new design strategy toward chemical threshold photoreaction.

  6. Near atomically smooth alkali antimonide photocathode thin films

    CERN Document Server

    Feng, Jun; Nasiatka, James; Schubert, Susanne; Smedley, John; Padmore, Howard


    Nano-roughness limits the emittance of electron beams that can be generated by high efficiency photocathodes, such as the thermally reacted alkali antimonide thin films. However there is an urgent need for photocathodes that can produce an order of magnitude or more lower emittance than present day systems in order to increase the transverse coherence width of the electron beam. In this paper we demonstrate a method for producing alkali antimonide cathodes with near atomic smoothness with high reproducibility.

  7. Estimating the hydration enthalpies of neutral alkali metal atoms. (United States)

    Stace, A J


    Using existing data on the ionization energies of alkali metal atoms in small clusters of water, a thermodynamic cycle is proposed from which the hydration enthalpies of the neutral metal atoms can be estimated. Where comparisons are possible, the results are in reasonable agreement with those obtained using both experimental and ab initio methods. Application of the thermodynamic cycle to neutral alkali metal atoms solvated in ammonia yields solvation enthalpies that are significantly lower than those obtained for water.

  8. Alkali promotion of N-2 dissociation over Ru(0001)

    DEFF Research Database (Denmark)

    Mortensen, Jens Jørgen; Hammer, Bjørk; Nørskov, Jens Kehlet


    Using self-consistent density functional calculations, we show that adsorbed Na and Cs lower the barrier for dissociation of N2 on Ru(0001). Since N2 dissociation is a crucial step in the ammonia synthesis reaction, we explain in this way the experimental observation that alkali metals promote...... the ammonia synthesis reaction over Ru catalysts. We also show that the origin of this effect is predominantly a direct electrostatic attraction between the adsorbed alkali atoms and the dissociating molecule....

  9. Photoemission spectroscopy study of a multi-alkali photocathode

    CERN Document Server

    Ettema, A R H


    In this paper a photoemission study of the highest core levels of the elements and the electron escape barrier (work function) in a multi-alkali photocathode are presented. The core levels indicate that the alkali atoms are in an oxidized state and therefore the compound Na sub 2 KSb can be regarded as an ionic semiconductor. The measured escape barrier of the Cs sub 2 O surface layer is determined as 2.3 eV.

  10. Alkali absorption and citrate excretion in calcium nephrolithiasis (United States)

    Sakhaee, K.; Williams, R. H.; Oh, M. S.; Padalino, P.; Adams-Huet, B.; Whitson, P.; Pak, C. Y.


    The role of net gastrointestinal (GI) alkali absorption in the development of hypocitraturia was investigated. The net GI absorption of alkali was estimated from the difference between simple urinary cations (Ca, Mg, Na, and K) and anions (Cl and P). In 131 normal subjects, the 24 h urinary citrate was positively correlated with the net GI absorption of alkali (r = 0.49, p < 0.001). In 11 patients with distal renal tubular acidosis (RTA), urinary citrate excretion was subnormal relative to net GI alkali absorption, with data from most patients residing outside the 95% confidence ellipse described for normal subjects. However, the normal relationship between urinary citrate and net absorbed alkali was maintained in 11 patients with chronic diarrheal syndrome (CDS) and in 124 stone-forming patients devoid of RTA or CDS, half of whom had "idiopathic" hypocitraturia. The 18 stone-forming patients without RTA or CDS received potassium citrate (30-60 mEq/day). Both urinary citrate and net GI alkali absorption increased, yielding a significantly positive correlation (r = 0.62, p < 0.0001), with the slope indistinguishable from that of normal subjects. Thus, urinary citrate was normally dependent on the net GI absorption of alkali. This dependence was less marked in RTA, confirming the renal origin of hypocitraturia. However, the normal dependence was maintained in CDS and in idiopathic hypocitraturia, suggesting that reduced citrate excretion was largely dietary in origin as a result of low net alkali absorption (from a probable relative deficiency of vegetables and fruits or a relative excess of animal proteins).

  11. Water Content of Lunar Alkali Fedlspar (United States)

    Mills, R. D.; Simon, J. I.; Wang, J.; Alexander, C. M. O'D.; Hauri, E. H.


    Detection of indigenous hydrogen in a diversity of lunar materials, including volcanic glass, melt inclusions, apatite, and plagioclase suggests water may have played a role in the chemical differentiation of the Moon. Spectroscopic data from the Moon indicate a positive correlation between water and Th. Modeling of lunar magma ocean crystallization predicts a similar chemical differentiation with the highest levels of water in the K- and Th-rich melt residuum of the magma ocean (i.e. urKREEP). Until now, the only sample-based estimates of water content of KREEP-rich magmas come from measurements of OH, F, and Cl in lunar apatites, which suggest a water concentration of water content of the magma ocean would have water contents of 320 ppm for the bulk Moon and 1.4 wt % for urKREEP from plagioclase in ferroan anorthosites. Results and interpretation: NanoSIMS data from granitic clasts from Apollo sample 15405,78 show that alkali feldspar, a common mineral in K-enriched rocks, can have approx. 20 ppm of water, which implies magmatic water contents of approx. 1 wt % in the high-silica magmas. This estimate is 2 to 3 orders of magnitude higher than that estimated from apatite in similar rocks. However, the Cl and F contents of apatite in chemically similar rocks suggest that these melts also had high Cl/F ratios, which leads to spuriously low water estimates from the apatite. We can only estimate the minimum water content of urKREEP (+ bulk Moon) from our alkali feldspar data because of the unknown amount of degassing that led to the formation of the granites. Assuming a reasonable 10 to 100 times enrichment of water from urKREEP into the granites produces an estimate of 100-1000 ppm of water for the urKREEP reservoir. Using the modeling of and the 100-1000 ppm of water in urKREEP suggests a minimum bulk silicate Moon water content between 2 and 20 ppm. However, hydrogen loss was likely very significant in the evolution of the lunar mantle. Conclusions: Lunar granites

  12. Absorption spectra of alkali-C₆₀ nanoclusters. (United States)

    Rabilloud, Franck


    We investigate the absorption spectra of alkali-doped C60 nanoclusters, namely C60Nan, C60Kn, and C60Lin, with n = 1, 2, 6, 12, in the framework of the time-dependent density-functional theory (TDDFT). We study the dependence of the absorption spectra on the nature of the alkali. We show that in few cases the absorption spectra depend on the arrangement of the alkali atoms over the fullerene, though sometimes the absorption spectra do not allow us to distinguish between different configurations. When only one or two alkali atoms are adsorbed on the fullerene, the optical response of alkali-doped C60 is similar to that of the anion C60(-) with a strong response in the UV domain. In contrast, for higher concentration of alkali, a strong optical response is predicted in the visible range, particularly when metal-metal bonds are formed. The weak optical response of the I(h)-symmetry C60Li12 is proposed to be used as a signature of its structure.

  13. Alkali-metal azides interacting with metal-organic frameworks. (United States)

    Armata, Nerina; Cortese, Remedios; Duca, Dario; Triolo, Roberto


    Interactions between alkali-metal azides and metal-organic framework (MOF) derivatives, namely, the first and third members of the isoreticular MOF (IRMOF) family, IRMOF-1 and IRMOF-3, are studied within the density functional theory (DFT) paradigm. The investigations take into account different models of the selected IRMOFs. The mutual influence between the alkali-metal azides and the π rings or Zn centers of the involved MOF derivatives are studied by considering the interactions both of the alkali-metal cations with model aromatic centers and of the alkali-metal azides with distinct sites of differently sized models of IRMOF-1 and IRMOF-3. Several exchange and correlation functionals are employed to calculate the corresponding interaction energies. Remarkably, it is found that, with increasing alkali-metal atom size, the latter decrease for cations interacting with the π-ring systems and increase for the azides interacting with the MOF fragments. The opposite behavior is explained by stabilization effects on the azide moieties and determined by the Zn atoms, which constitute the inorganic vertices of the IRMOF species. Larger cations can, in fact, coordinate more efficiently to both the aromatic center and the azide anion, and thus stabilizing bridging arrangements of the azide between one alkali-metal and two Zn atoms in an η(2) coordination mode are more favored.

  14. Two-phase alkali-metal experiments in reduced gravity

    Energy Technology Data Exchange (ETDEWEB)

    Antoniak, Z.I.


    Future space missions envision the use of large nuclear reactors utilizing either a single or a two-phase alkali-metal working fluid. The design and analysis of such reactors require state-of-the-art computer codes that can properly treat alkali-metal flow and heat transfer in a reduced-gravity environment. A literature search of relevant experiments in reduced gravity is reported on here, and reveals a paucity of data for such correlations. The few ongoing experiments in reduced gravity are noted. General plans are put forth for the reduced-gravity experiments which will have to be performed, at NASA facilities, with benign fluids. A similar situation exists regarding two-phase alkali-metal flow and heat transfer, even in normal gravity. Existing data are conflicting and indequate for the task of modeling a space reactor using a two-phase alkali-metal coolant. The major features of past experiments are described here. Data from the reduced-gravity experiments with innocuous fluids are to be combined with normal gravity data from the two-phase alkali-metal experiments. Analyses undertaken here give every expectation that the correlations developed from this data base will provide a valid representation of alkali-metal heat transfer and pressure drop in reduced gravity.


    Directory of Open Access Journals (Sweden)

    Bwire S. Ndazi


    Full Text Available Chemical and thermal stability of rice husks against alkali treatment with 2 to 8% w/v NaOH are presented and discussed in this paper. The thermal stability of the rice husks was examined by using a thermal gravimetric analysis instrument. Chemical stability was evaluated by examining the organic components of rice husks using proximate analysis. The results indicated that the proportion of lignin and hemicellulose in rice husks treated with NaOH ranging from 4 to 8% decreased significantly by 96% and 74%, respectively. The thermal stability and final degradation temperatures of the alkali-treated rice husks were also lowered by 24-26°C due to degradation of hemicellulose and lignin during alkali treatment. Absence of the onset degradation zones in the alkali-treated rice husks was a further indication that hemicellulose and other volatile substances degraded during alkali treatment. This leads to a conclusion that alkali treatment of rice husks with more than 4% NaOH causes a substantial chemical degradation of rice husks, which subsequently decreases their thermal stability.

  16. Vibrations of alkali metal overlayers on metal surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Rusina, G G; Eremeev, S V; Borisova, S D [Institute of Strength Physics and Materials Science SB RAS, 634021, Tomsk (Russian Federation); Echenique, P M; Chulkov, E V [Donostia International Physics Center (DIPC), 20018 San Sebastian/Donostia, Basque Country (Spain); Benedek, G [Dipartimento di Scienza dei Materiali, Universita di Milano-Bicocca, Via Cozzi 53, 20125 Milano (Italy)], E-mail:


    We review the current progress in the understanding of vibrations of alkalis adsorbed on metal surfaces. The analysis of alkali vibrations was made on the basis of available theoretical and experimental results. We also include in this discussion our recent calculations of vibrations in K/Pt(111) and Li(Na)/Cu(001) systems. The dependence of alkali adlayer localized modes on atomic mass, adsorption position and coverage as well as the dependence of vertical vibration frequency on the substrate orientation is discussed. The square root of atomic mass dependence of the vertical vibration energy has been confirmed by using computational data for alkalis on the Al(111) and Cu(001) substrates. We have confirmed that in a wide range of submonolayer coverages the stretch mode energy remains nearly constant while the energy of in-plane polarized modes increases with the increase of alkali coverage. It was shown that the spectrum of both stretch and in-plane vibrations can be very sensitive to the adsorption position of alkali atoms and substrate orientation.

  17. Vibrations of alkali metal overlayers on metal surfaces (United States)

    Rusina, G. G.; Eremeev, S. V.; Echenique, P. M.; Benedek, G.; Borisova, S. D.; Chulkov, E. V.


    We review the current progress in the understanding of vibrations of alkalis adsorbed on metal surfaces. The analysis of alkali vibrations was made on the basis of available theoretical and experimental results. We also include in this discussion our recent calculations of vibrations in K/Pt(111) and Li(Na)/Cu(001) systems. The dependence of alkali adlayer localized modes on atomic mass, adsorption position and coverage as well as the dependence of vertical vibration frequency on the substrate orientation is discussed. The square root of atomic mass dependence of the vertical vibration energy has been confirmed by using computational data for alkalis on the Al(111) and Cu(001) substrates. We have confirmed that in a wide range of submonolayer coverages the stretch mode energy remains nearly constant while the energy of in-plane polarized modes increases with the increase of alkali coverage. It was shown that the spectrum of both stretch and in-plane vibrations can be very sensitive to the adsorption position of alkali atoms and substrate orientation.


    Directory of Open Access Journals (Sweden)



    Full Text Available ABSTRACT: AIM: This study evaluated the antibacterial effect of ca lcium hydroxide in different vehicles in an in vitro model. MATERIAL AND METHODS: Calcium hydroxide paste prepared with two conventionally used vehicles namely, campho rated monochlophenol, distilled water and also propylene glycol. The antibacterial activity of these paste were tested against five micro- organisms that can commonly occur in the inf ected root canals. RESULTS AND CONCLUSIONS: The results of the study indicate that a paste of ca lcium hydroxide made with propylene glycol exerts significant antibacterial act ion. Hence, it can be recommended for use as an intracanal medicament in preference to a paste prepa red with a tissue toxic phenolic compound like camphorated mono chlorophenol

  19. Structure and properties of porous ceramics obtained from aluminum hydroxide (United States)

    Levkov, R.; Kulkov, S.


    In this paper the study of porous ceramics obtained from aluminum hydroxide with gibbsite modification is presented. The dependence of porosity and mechanical characteristics of the material sintered at different temperatures was studied. It was shown that compressive strength of alumina ceramics increases by 40 times with decreasing the pore volume from 65 to 15%. It was shown that aluminum hydroxide may be used for pore formation and pore volume in the sintered ceramics can be controlled by varying the aluminum hydroxide concentration and sintering temperature. Based on these results one can conclude that the obtained structure is very close to inorganic bone matrix and can be used as promising material for bone implants production.

  20. Alkali and heavy metal emissions of the PCFB-process; Alkali- ja raskasmetallipaeaestoet PCFB-prosessista

    Energy Technology Data Exchange (ETDEWEB)

    Kuivalainen, R.; Eriksson, T.; Lehtonen, P. [Foster Wheeler Energia Oy, Karhula (Finland)


    Pressurized Circulating Fluidized Bed (PCFB) combustion technology has been developed in Karhula R and D Center since 1986. As part of the development, 10 MW PCFB test facility was built in 1989. The test facility has been used for performance testing with different coal types through the years 1990-1995 in order to gain data for design and commercialization of the high-efficiency low-emission PCFB combustion technology. The main object of the project was to measure vapor phase Na and K concentrations in the PCFB flue gas after hot gas filter and investigate the effects of process conditions and sorbents on alkali release. The measurements were performed using plasma assisted method of TUT Laboratory of Plasma Technology and wet absorption method of VTT Energy. The measurements were carried out during three test campaigns at PCFB Test Facility in Karhula. In autumn 1995 both VTT and TUT methods were used. The measurements of the following test period in spring 1996 were performed by VTT, and during the last test segment in autumn 1996 TUT method was in use. During the last test period, the TUT instrument was used as semi-continuous (3 values/minute) alkali analyzer for part of the time. The measured Na concentrations were below 30 ppb(w) in all measured data points. The results of K were below 10 ppb(w). The accuracies of the both methods are about +50 % at this concentration range. The scatter of the data covers the effects of different process variables on the alkali emission. The measured emissions are at the same order of magnitude as the guideline emission limits estimated by gas turbine manufacturers

  1. Relation between the electroforming voltage in alkali halide-polymer diodes and the bandgap of the alkali halide

    Energy Technology Data Exchange (ETDEWEB)

    Bory, Benjamin F.; Wang, Jingxin; Janssen, René A. J.; Meskers, Stefan C. J., E-mail: [Molecular Materials and Nanosystems and Institute for Complex Molecular Systems, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven (Netherlands); Gomes, Henrique L. [Instituto de Telecomunicações, Av. Rovisco, Pais 1, 1049-001 Lisboa, Portugal and Universidade do Algarve, Campus de Gambelas, 8005-139 Faro (Portugal); De Leeuw, Dago M. [Max-Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany and King Abdulaziz University, Jeddah (Saudi Arabia)


    Electroforming of indium-tin-oxide/alkali halide/poly(spirofluorene)/Ba/Al diodes has been investigated by bias dependent reflectivity measurements. The threshold voltages for electrocoloration and electroforming are independent of layer thickness and correlate with the bandgap of the alkali halide. We argue that the origin is voltage induced defect formation. Frenkel defect pairs are formed by electron–hole recombination in the alkali halide. This self-accelerating process mitigates injection barriers. The dynamic junction formation is compared to that of a light emitting electrochemical cell. A critical defect density for electroforming is 10{sup 25}/m{sup 3}. The electroformed alkali halide layer can be considered as a highly doped semiconductor with metallic transport characteristics.

  2. Superconductivity in alkali-metal-doped picene. (United States)

    Mitsuhashi, Ryoji; Suzuki, Yuta; Yamanari, Yusuke; Mitamura, Hiroki; Kambe, Takashi; Ikeda, Naoshi; Okamoto, Hideki; Fujiwara, Akihiko; Yamaji, Minoru; Kawasaki, Naoko; Maniwa, Yutaka; Kubozono, Yoshihiro


    Efforts to identify and develop new superconducting materials continue apace, motivated by both fundamental science and the prospects for application. For example, several new superconducting material systems have been developed in the recent past, including calcium-intercalated graphite compounds, boron-doped diamond and-most prominently-iron arsenides such as LaO(1-x)F(x)FeAs (ref. 3). In the case of organic superconductors, however, no new material system with a high superconducting transition temperature (T(c)) has been discovered in the past decade. Here we report that intercalating an alkali metal into picene, a wide-bandgap semiconducting solid hydrocarbon, produces metallic behaviour and superconductivity. Solid potassium-intercalated picene (K(x)picene) shows T(c) values of 7 K and 18 K, depending on the metal content. The drop of magnetization in K(x)picene solids at the transition temperature is sharp (<2 K), similar to the behaviour of Ca-intercalated graphite. The T(c) of 18 K is comparable to that of K-intercalated C(60) (ref. 4). This discovery of superconductivity in K(x)picene shows that organic hydrocarbons are promising candidates for improved T(c) values.

  3. Bioinorganic Chemistry of the Alkali Metal Ions. (United States)

    Kim, Youngsam; Nguyen, Thuy-Tien T; Churchill, David G


    The common Group 1 alkali metals are indeed ubiquitous on earth, in the oceans and in biological systems. In this introductory chapter, concepts involving aqueous chemistry and aspects of general coordination chemistry and oxygen atom donor chemistry are introduced. Also, there are nuclear isotopes of importance. A general discussion of Group 1 begins from the prevalence of the ions, and from a comparison of their ionic radii and ionization energies. While oxygen and water molecule binding have the most relevance to biology and in forming a detailed understanding between the elements, there is a wide range of basic chemistry that is potentially important, especially with respect to biological chelation and synthetic multi-dentate ligand design. The elements are widely distributed in life forms, in the terrestrial environment and in the oceans. The details about the workings in animal, as well as plant life are presented in this volume. Important biometallic aspects of human health and medicine are introduced as well. Seeing as the elements are widely present in biology, various particular endogenous molecules and enzymatic systems can be studied. Sodium and potassium are by far the most important and central elements for consideration. Aspects of lithium, rubidium, cesium and francium chemistry are also included; they help in making important comparisons related to the coordination chemistry of Na(+) and K(+). Physical methods are also introduced.

  4. Superconductivity in alkali-doped fullerene nanowhiskers (United States)

    Takeya, Hiroyuki; Konno, Toshio; Hirata, Chika; Wakahara, Takatsugu; Miyazawa, Kun'ichi; Yamaguchi, Takahide; Tanaka, Masashi; Takano, Yoshihiko


    Superconductivity in alkali metal-doped fullerene nanowhiskers (C60NWs) was observed in K3.3C60NWs, Rb3.0C60NWs and Cs2.0Rb1.0C60NWs with transition temperatures at 17, 25 and 26 K, respectively. Almost full shielding volume fraction (~80%) was observed in K3.3C60NWs when subjected to thermal treatment at 200 °C for a duration of 24 h. In contrast, the shielding fraction of Rb3.0C60NWs and Cs2.0Rb1.0C60NWs were calculated to be 8% and 6%, respectively. Here we report on an extensive investigation of the superconducting properties of these AC60NWs (A  =  K3.3, Rb3.0 and Cs2.0Rb1.0). These properties are compared to the ones reported on the corresponding conventional (single-crystal or powder) K-doped fullerene. We also evaluated the critical current densities of these C60NWs using the Bean model under an applied magnetic field up to 50 kOe.

  5. Alternative alkali resistant deNOx catalysts

    DEFF Research Database (Denmark)

    Putluru, Siva Sankar Reddy; Kristensen, Steffen Buus; Due-Hansen, Johannes;


    Alternative alkali resistant deNOx catalysts were prepared using three different supports ZrO2, TiO2 and Mordenite zeolite. The majority of the catalysts were prepared by incipient wetness impregnation of a commercial support, with vanadium, copper or iron precursor, one catalyst was prepared...... by onepot sol–gel method. All catalysts were characterized by BET, XRPD and NH3-TPD. Initial SCR activities of 8 out of 9 catalysts showed higher NO conversion at least at one temperature in the temperature range 300–500 ◦C compared to the conventional V2O5-WO3/TiO2 catalyst. After potassium poisoning (100......–130 µmol of K/g of catalyst) the relative drop in SCR activity and acidity was lower for all the alternative catalysts compared to the industrial V2O5-WO3/TiO2 catalyst. Furthermore, Cu/MOR and Nano-V2O5/Sul-TiO2 catalysts showed 8–16 times higher SCR activities than the conventional even after high...

  6. Oxidative leaching of chromium from layered double hydroxides: Mechanistic studies

    Indian Academy of Sciences (India)

    A V Radha; P Vishnu Kamath


    The layered double hydroxide (LDH) of Zn with Cr on treatment with a hypochlorite solution releases chromate ions as a result of oxidative leaching by a dissolution–reprecipitation mechanism. The residue is found to be -Zn(OH)2. The LDH of Mg with Cr on the other hand is resistant to oxidative leaching. In contrast, a X-ray amorphous gel of the coprecipitated hydroxides of Mg and Cr yields chromate ions. These results suggest that the oxidation potential of Cr(III) in LDHs is determined by the nature of the divalent ion and the crystallinity of the phase while being unaffected by the nature of the intercalated anions.

  7. Alkali-aggregate reactivity of typical siliceious glass and carbonate rocks in alkali-activated fly ash based geopolymers (United States)

    Lu, Duyou; Liu, Yongdao; Zheng, Yanzeng; Xu, Zhongzi; Shen, Xiaodong


    For exploring the behaviour of alkali-aggregate reactivity (AAR) in alkali-activated geopolymeric materials and assessing the procedures for testing AAR in geopolymers, the expansion behaviour of fly ash based geopolymer mortars with pure silica glass and typical carbonate rocks were studied respectively by curing at various conditions, i.e. 23°C and 38°C with relative humidity over 95%, immersed in 1M NaOH solution at 80°C. Results show that, at various curing conditions, neither harmful ASR nor harmful ACR was observed in geopolymers with the criteria specified for OPC system. However, with the change of curing conditions, the geopolymer binder and reactive aggregates may experience different reaction processes leading to quite different dimensional changes, especially with additional alkalis and elevated temperatures. It suggests that high temperature with additional alkali for accelerating AAR in traditional OPC system may not appropriate for assessing the alkali-aggregate reactivity behaviour in geopolymers designed for normal conditions. On the other hand, it is hopeful to control the dimensional change of geopolymer mortar or concrete by selecting the type of aggregates and the appropriate curing conditions, thus changing the harmful AAR in OPC into beneficial AAR in geopolymers and other alkali-activated cementitious systems.

  8. Interactions and low energy collisions between an alkali ion and an alkali atom of different nucleus

    CERN Document Server

    Rakshit, Arpita; Berriche, Hamid; Deb, Bimalendu


    We study theoretically interaction potentials and low energy collisions between different alkali atoms and alkali ions. Specifically, we consider systems like X + Y$^{+}$, where X(Y$^{+})$ is either Li(Cs$^+$) or Cs((Li$^+$), Na(Cs$^+$) or Cs(Na$^+$) and Li(Rb$^+$) or Rb(Li$^+$). We calculate the molecular potentials of the ground and first two excited states of these three systems using pseudopotential method and compare our results with those obtained by others. We calculate ground-state scattering wave functions and cross sections of these systems for a wide range of energies. We find that, in order to get convergent results for the total scattering cross sections for energies of the order $1$ K, one needs to take into account at least 60 partial waves. In the low energy limit ($< 1 \\mu$K), elastic scattering cross sections exhibit Wigner law threshold behavior while in the high energy limit the cross sections go as $E^{-1/3}$. We discuss qualitatively the possibilities of forming cold molecular ion by ...

  9. From Zn-Al layered double hydroxide to ZnO nanostructure:Gradually etching by sodium hydroxide

    Institute of Scientific and Technical Information of China (English)

    Gang Qiang Wan; Dong Xiang Li; Chun Fang Li; Jie Xu; Wan Guo Hou


    Zn-Al layered double hydroxide (LDH) was used as precursor to produce ZnO nanostructures through dissolution of aluminum hydroxide in caustic soda.The Zn-Al LDH could transform into different nanostructures of ZnO on LDH nanosheets and even pure ZnO nanorods under various NaOH concentration.The formed ZnO nanorods vertically aligned on both LDH sides.UV-vis diverse reflectance spectra show that the obtained ZnO nanorods have a band gap of approximately 3.05 eV.Such ZnO/LDH nanostructures might be used as photocatalyst in the organic pollutant decomposition.

  10. Alkali norite, troctolites, and VHK mare basalts from breccia 14304 (United States)

    Goodrich, Cyrena Anne; Taylor, G. Jeffrey; Keil, Klaus; Kallemeyn, Gregory W.; Warren, Paul H.


    Twelve clasts were separated from breccia 14304 for consortium study: six pristine highlands rocks, two mare basalts, and four nonpristine highlands rocks. The pristine highlands rocks include representatives of the magnesian troctolite-anorthosite and alkali suites, the two most common subgroups of the Mg suite found at the Apollo 14 site. Two troctolite clasts have olivine (~Fo 90) and plagioclase (~An 94) compositions similar to one group of Apolo 14 troctolites. One also contains spinel (Mg' 66-85). Incompatible element abundances in one are similar to those of 14305 troctolites, although the HREE (heavy rare earth elements) pattern is distinct among Apollo 14 troctolites. A dunite clast (~Fo 89) may be an unrepresentative piece of a troctolite. Alkali lithologies include an alkali anorthosite and an alkali norite, which is a rock type not previously described. The alkali norite has a pristine igneous texture and contains inverted pigeonite (Mg' 64), plagioclase (An82), K-feldspar, ternary feldspar, REE-rich phosphates, and silica. It resembles alkali gabbronorites from Apollo 14 and 67975 in mineralogy and mineral compositions. Alkali lithologies and phosphate-bearing magnesian anorthosites from Apollo 14 may have formed from Mg-rich magmas that assimilated various amounts of material rich in P and REE. This material could be a fractionated derivative of urKREEP. another pristine clast from 14304 is an Mg-gabbronorite. The two mare basalt clasts are very high potassium (VHK) basalts. They have 4 mg/g K and K/La ratios of 580 and 700. The parent magmas of VHK basalts could have formed from typical low-Ti, high-Al basaltic magmas by assimilation of K-rich material. This material could also be a fractionated derivative or urKREEP. Nonpristine 14304 clasts include melt-textured anorthosites and an augite-rich poikilitic melt rock. The latter is probably polymict, but its major component must be an Mg-suite gabbro.

  11. Molecular photons interfaced with alkali atoms. (United States)

    Siyushev, Petr; Stein, Guilherme; Wrachtrup, Jörg; Gerhardt, Ilja


    Future quantum communication will rely on the integration of single-photon sources, quantum memories and systems with strong single-photon nonlinearities. Two key parameters are crucial for the single-photon source: a high photon flux with a very small bandwidth, and a spectral match to other components of the system. Atoms or ions may act as single-photon sources--owing to their narrowband emission and their intrinsic spectral match to other atomic systems--and can serve as quantum nonlinear elements. Unfortunately, their emission rates are still limited, even for highly efficient cavity designs. Single solid-state emitters such as single organic dye molecules are significantly brighter and allow for narrowband photons; they have shown potential in a variety of quantum optical experiments but have yet to be interfaced with other components such as stationary memory qubits. Here we describe the optical interaction between Fourier-limited photons from a single organic molecule and atomic alkali vapours, which can constitute an efficient quantum memory. Single-photon emission rates reach up to several hundred thousand counts per second and show a high spectral brightness of 30,000 detectable photons per second per megahertz of bandwidth. The molecular emission is robust and we demonstrate perfect tuning to the spectral transitions of the sodium D line and efficient filtering, even for emitters at ambient conditions. In addition, we achieve storage of molecular photons originating from a single dibenzanthanthrene molecule in atomic sodium vapour. Given the large set of molecular emission lines matching to atomic transitions, our results enable the combination of almost ideal single-photon sources with various atomic vapours, such that experiments with giant single-photon nonlinearities, mediated, for example, by Rydberg atoms, become feasible.

  12. Recent progress in polymer/layered double hydroxide nanocomposites

    Institute of Scientific and Technical Information of China (English)

    DING Peng; CHEN Wei; QU Baojun


    New developments in the studies of nanocomposites based on polymer matrixes and layered double hydroxides (LDHs)in recent years are reviewed combining our relative research work, among which the synthesis techniques, the physicochemical characterizations, and the improved material properties are especially discussed. The possible application of polymer/LDH nanocomposites is also proposed.

  13. Sorptive stabilization of organic matter by amorphous Al hydroxide

    NARCIS (Netherlands)

    M.P.W. Schneider; T. Scheel; R. Mikutta; P. van Hees; K. Kaiser; K. Kalbitz


    Amorphous Al hydroxides (am-Al(OH)(3)) strongly sorb and by this means likely protect dissolved organic matter (OM) against microbial decay in soils. We carried out batch sorption experiments (pH 4.5; 40 mg organic C L-1) with OM extracted from organic horizons under a Norway spruce and a European b

  14. Dewatering of alumino-humic sludge: impacts of hydroxide. (United States)

    Bache, D H; Papavasilopoulos, E N


    The paper draws together information on factors which influence the conditioning and dewatering behaviour of an alum sludge gained from the coagulation of a low-turbidity coloured water. A principal focus is the potential impact of aluminium hydroxide on the sludge character. Background information is provided on the composition of the source floc for the domain pH 6.0-6.5 and Al>2.0mg/l. From this, there were many pointers to the presence of Al(OH)(3)(s) within the floc. A series of comparisons were made between an alum sludge and a hydroxide suspension at a concentration equivalent to the coagulant fraction within the sludge. The parameters studied included floc size, floc density, polymer adsorption and dewatering behaviour at different time-scales. In all cases, there were strong similarities in the behaviour of the two suspensions-indicating the potential impact of the hydroxide. There was also evidence of common features being displayed by both the organic fractions and the hydroxide. It was suggested that some of the behavioural features might emanate from a common fractal structure within the source floc, the fractal dimension (approximately 1) being insensitive to composition.

  15. 21 CFR 73.1010 - Alumina (dried aluminum hydroxide). (United States)


    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Alumina (dried aluminum hydroxide). 73.1010 Section 73.1010 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES GENERAL LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION Drugs § 73.1010 Alumina (dried...


    Energy Technology Data Exchange (ETDEWEB)



    This document generates a supernatant hydroxide ion depletion model based on mechanistic principles. The carbon dioxide absorption mechanistic model is developed in this report. The report also benchmarks the model against historical tank supernatant hydroxide data and vapor space carbon dioxide data. A comparison of the newly generated mechanistic model with previously applied empirical hydroxide depletion equations is also performed.

  17. Nature of the Charge Localized Between Alkali Adatoms and Metal Substrates


    Wertheim, G. K.; Riffe, D. Mark; Citrin, P. H.


    Two previously unappreciated features in photoemission spectra from alkali atoms adsorbed on W(110), namely, the sign of the alkali-induced surface-atom core-level shift of the substrate at low coverage and the very large alkali shallow core-hole lifetime width at all coverages, show that the alkali-substrate interaction is not well described by a transfer of alkali charge. Instead, both features point to the formation of a charge cloud between the alkali adatom and substrate that is d...

  18. Multi-photon processes in alkali metal vapors (United States)

    Gai, Baodong; Hu, Shu; Li, Hui; Shi, Zhe; Cai, Xianglong; Guo, Jingwei; Tan, Yannan; Liu, Wanfa; Jin, Yuqi; Sang, Fengting


    Achieving population inversion through multi-photon cascade pumping is almost always difficult, and most laser medium work under 1-photon excitation mechanism. But for alkali atoms such as cesium, relatively large absorption cross sections of several low, cascading energy levels enable them properties such as up conversion. Here we carried out research on two-photon excitation alkali fluorescence. Two photons of near infrared region are used to excite alkali atoms to n 2 D5/2, n 2 D3/2 or higher energy levels, then the blue fluorescence of (n+1) 2 P3/2,(n+1) 2 P1/2-->n 2 S1/2 are observed. Different pumping paths are tried and by the recorded spectra, transition routes of cesium are deducted and concluded. Finally the possibility of two-photon style DPALs (diode pumped alkali laser) are discussed, such alkali lasers can give output wavelengths in the shorter end of visual spectroscopy (400-460 nm) and are expected to get application in underwater communication and material laser processing.

  19. The Impact of Post-Pretreatment Conditioning on Enzyme Accessibility and Water Interactions in Alkali Pretreated Rice Straw (United States)

    Karuna, Nardrapee

    Rice straw, a high-abundance lignocellulosic residue from rice production has tremendous potential as a feedstock for biofuel production in California. In this study, the impact of post-alkali pretreatment conditioning schemes on enzyme saccharification efficiency was examined, particularly focusing on understanding resulting biomass compositional impacts on water interactions with the biomass and enzyme accessibility to the cellulose fraction. Rice straw was pretreated with sodium hydroxide and subsequently washed by two different conditions: 1) by extensive washing with distilled water to reduce the pH to the optimum for cellulases which is pH 5--6, and 2) immediate pH adjustment to pH 5--6 with hydrochloric acid before extensive washing with distilled water. The two post-pretreatment conditions gave significant differences in ash, acid-insoluble lignin, glucan and xylan compositions. Alkali pretreatment improved cellulase digestibility of rice straw, and water washing improved enzymatic digestibility more than neutralization. Hydrolysis reactions with a purified Trichoderma reesei Cel7A, a reducing-end specific cellulase, demonstrated that the differences in saccharification are likely due to differences in the accessibility of the cellulose fraction to the cellulolytic enzymes. Further analyses were conducted to study the mobility of the water associated with the rice straw samples by measuring T2 relaxation times of the water protons by 1H-Nuclear Magnetic Resonance (NMR) relaxometry. Results showed significant changes in water association with the rice straw due to the pretreatment and due to the two different post-pretreatment conditions. Pretreatment increased the amount of water at the surface of the rice straw samples as indicated by increased amplitude of the shortest T2 time peaks in the relaxation spectra. Moreover, the amount of water in the first T2 pool in the water washed sample was significantly greater than in the neutralized sample. These

  20. Maternal exposure to alkali, alkali earth, transition and other metals: Concentrations and predictors of exposure. (United States)

    Hinwood, A L; Stasinska, A; Callan, A C; Heyworth, J; Ramalingam, M; Boyce, M; McCafferty, P; Odland, J Ø


    Most studies of metals exposure focus on the heavy metals. There are many other metals (the transition, alkali and alkaline earth metals in particular) in common use in electronics, defense industries, emitted via combustion and which are naturally present in the environment, that have received limited attention in terms of human exposure. We analysed samples of whole blood (172), urine (173) and drinking water (172) for antimony, beryllium, bismuth, cesium, gallium, rubidium, silver, strontium, thallium, thorium and vanadium using ICPMS. In general most metals concentrations were low and below the analytical limit of detection with some high concentrations observed. Few factors examined in regression models were shown to influence biological metals concentrations and explained little of the variation. Further study is required to establish the source of metals exposures at the high end of the ranges of concentrations measured and the potential for any adverse health impacts in children.

  1. Hydrothermal synthesis of K2CO3-promoted hydrotalcite from hydroxide-form precursors for novel high-temperature CO2 sorbent. (United States)

    Jang, Hee Jin; Lee, Chan Hyun; Kim, Suji; Kim, Sung Hyun; Lee, Ki Bong


    In many materials for CO2 sorption, hydrotalcite is attracting substantial attention as a high temperature (200-500 °C) CO2 sorbent because of its fast sorption/desorption kinetics and easy regenerability. However, the CO2-sorption capacity of conventional hydrotalcite is relatively low for large-scale commercial use. To enhance CO2-sorption capacity, hydrotalcite is conventionally impregnated with alkali metals such as K2CO3. Although K2CO3-impregnated hydrotalcite has high CO2-sorption capacity, the preparation method takes long time and is inconvenient because hydrotalcite synthesis step and alkali metal impregnation step are separated. In this study, K2CO3-promoted hydrotalcite was newly synthesized from hydroxide-form percursors by a simple and eco-friendly method without a solvent-consuming washing step. Analysis based on X-ray diffraction indicated that the prepared samples had structures of well-defined hydrotalcite crystalline and un-reacted Mg(OH)2 precursor. Moreover, K2CO3 was successfully incorporated in hydrotalcite during the synthesis step. The prepared K2CO3-promoted hydrotalcite showed high CO2-sorption capacity and had potential for use as a high-temperature CO2 sorbent.

  2. Characterization of alkali-modified soy protein concentrate

    Directory of Open Access Journals (Sweden)

    Barać Miroljub B.


    Full Text Available To study the influence of the preparation mode, including mild alkali modification, of soy protein concentrate on soluble protein content and composition, some of its nutritive and functional properties were investigated. Soy protein concentrate prepared by aqueous alcohol leaching was modified in mild alkaline solutions (pH 8.0 at 40, 50 and 60° C for 60 minutes and compared with two principal types of commercial soy protein concentrate. Soluble protein content, composition and properties of soy protein concentrate, as well as their potential use are essentially determined by the preparation mode. Limited mild alkali hydrolysis increased protein solubility by 40-71%, while emulsion stability was increased by 18-56%. Major storage soybean proteins exhibited different stability to alcohol denaturation and mild alkali modification. The most susceptible were acidic -A3 - and -A5- subunits of glycinin.

  3. Orbital Feshbach Resonance in Alkali-Earth Atoms. (United States)

    Zhang, Ren; Cheng, Yanting; Zhai, Hui; Zhang, Peng


    For a mixture of alkali-earth atomic gas in the long-lived excited state ^{3}P_{0} and the ground state ^{1}S_{0}, in addition to nuclear spin, another "orbital" index is introduced to distinguish these two internal states. In this Letter we propose a mechanism to induce Feshbach resonance between two atoms with different orbital and nuclear spin quantum numbers. Two essential ingredients are the interorbital spin-exchange process and orbital dependence of the Landé g factors. Here the orbital degrees of freedom plays a similar role as the electron spin degree of freedom in magnetic Feshbach resonance in alkali-metal atoms. This resonance is particularly accessible for the ^{173}Yb system. The BCS-BEC crossover in this system requires two fermion pairing order parameters, and displays a significant difference compared to that in an alkali-metal system.

  4. Oscillation Frequencies for Simultaneous Trapping of Heteronuclear Alkali Atoms

    CERN Document Server

    Kaur, Kiranpreet; Arora, Bindiya


    We investigate oscillation frequencies for simultaneous trapping of more than one type of alkali atoms in a common optical lattice. For this purpose, we present numerical results for magic trapping conditions, where the oscillation frequencies for two different kind of alkali atoms using laser lights in the wavelength range 500-1200 nm are same. These wavelengths will be of immense interest for studying static and dynamic properties of boson-boson, boson-fermion, fermion-fermion, and boson-boson-boson mixtures involving different isotopes of Li, Na, K, Rb, Cs and Fr alkali atoms. In addition to this, we were also able to locate a magic wavelength around 808.1 nm where all the three Li, K, and Rb atoms are found to be suitable for oscillating at the same frequency in a common optical trap.

  5. Formation and Stability of High-Spin Alkali Clusters (United States)

    Schulz, C. P.; Claas, P.; Schumacher, D.; Stienkemeier, F.


    Helium nanodroplet isolation has been applied to agglomerate alkali clusters at temperatures of 380mK. The very weak binding to the surface of the droplets allows a selection of only weakly bound, high-spin states. Here we show that larger clusters of alkali atoms in high-spin states can be formed. The lack of strong bonds from pairing electrons makes these systems nonmetallic, vanderWaals like complexes of metal atoms. We find that sodium and potassium readily form such clusters containing up to 25atoms. In contrast, this process is suppressed for rubidium and cesium. Apparently, for these heavy alkalis, larger high-spin aggregates are not stable and depolarize spontaneously upon cluster formation.

  6. Neuropsychiatric manifestations of alkali metal deficiency and excess

    Energy Technology Data Exchange (ETDEWEB)

    Yung, C.Y.


    The alkali metals from the Group IA of the periodic table (lithium, sodium, potassium, rubidium, cesium and francium) are reviewed. The neuropsychiatric aspects of alkali metal deficiencies and excesses (intoxications) are described. Emphasis was placed on lithium due to its clinical uses. The signs and symptoms of these conditions are characterized by features of an organic brain syndrome with delirium and encephalopathy prevailing. There are no clinically distinctive features that could be reliably used for diagnoses. Sodium and potassium are two essential alkali metals in man. Lithium is used as therapeutic agent in bipolar affective disorders. Rubidium has been investigated for its antidepressant effect in a group of psychiatric disorders. Cesium is under laboratory investigation for its role in carcinogenesis and in depressive illness. Very little is known of francium due to its great instability for experimental study.

  7. Low-frequency Raman scattering in alkali tellurite glasses

    Indian Academy of Sciences (India)

    Angelos G Kalampounias


    Raman scattering has been employed to study the alkali-cation size dependence and the polarization characteristics of the low-frequency modes for the glass-forming tellurite mixtures, 0.1M2O–0.9TeO2 (M = Na, K, Rb and Cs). The analysis has shown that the Raman coupling coefficient alters by varying the type of the alkali cation. The addition of alkali modifier in the tellurite network leads to the conversion of the TeO4 units to TeO3 units with a varying number of non-bridging oxygen atoms. Emphasis has also been given to the lowfrequency modes and particular points related to the low-frequency Raman phenomenology are discussed in view of the experimental findings.

  8. Alkali control of high-grade metamorphism and granitization

    Directory of Open Access Journals (Sweden)

    Oleg G. Safonov


    Full Text Available We review petrologic observations of reaction textures from high-grade rocks that suggest the passage of fluids with variable alkali activities. Development of these reaction textures is accompanied by regular compositional variations in plagioclase, pyroxenes, biotite, amphibole and garnet. The textures are interpreted in terms of exchange and net-transfer reactions controlled by the K and Na activities in the fluids. On the regional scale, these reactions operate in granitized, charnockitized, syenitized etc. shear zones within high-grade complexes. Thermodynamic calculations in simple chemical systems show that changes in mineral assemblages, including the transition from the hydrous to the anhydrous ones, may occur at constant pressure and temperature due only to variations in the H2O and the alkali activities. A simple procedure for estimating the activity of the two major alkali oxides, K2O and Na2O, is implemented in the TWQ software. Examples of calculations are presented for well-documented dehydration zones from South Africa, southern India, and Sri Lanka. The calculations have revealed two end-member regimes of alkalis during specific metamorphic processes: rock buffered, which is characteristic for the precursor rocks containing two feldspars, and fluid-buffered for the precursor rocks without K-feldspar. The observed reaction textures and the results of thermodynamic modeling are compared with the results of available experimental studies on the interaction of the alkali chloride and carbonate-bearing fluids with metamorphic rocks at mid-crustal conditions. The experiments show the complex effect of alkali activities in the fluid phase on the mineral assemblages. Both thermodynamic calculations and experiments closely reproduce paragenetic relations theoretically predicted by D.S. Korzhinskii in the 1940s.

  9. A hidden history of heartburn: The milk-alkali syndrome. (United States)

    Swaminathan, Krishnan


    Milk-alkali syndrome was once considered to be of historic interest and a rare cause of hypercalcemia. Currently, it should be an important consideration in the differential diagnosis of hypercalcemia, after malignancies and primary hyperparathyroidism. The resurgence is in part due to the easy availability of over the counter (OTC) calcium preparations. We describe a 50-year-old man who presented with severe hypercalcemia on two occasions associated with renal failure and metabolic alkalosis. Extensive investigations during the first admission failed to unravel a specific cause of hypercalcemia but a thorough history during his subsequent admission helped to confirm the diagnosis of milk-alkali syndrome.


    Institute of Scientific and Technical Information of China (English)

    LIU Xianfan; YANG Zhengxi; LIU Jiaduo; ZHANG Chengjiang; WU Dechao; LI Youguo


    Ultramafic hypoxenoliths found in the alkali-rich porphyry in the Liuhe Village, Heqing, Yunnan,China, are of great significance in understanding the origin and evolution of the porphyry. This paper discusses the mineralogical features of the hypoxenoliths. It shows that the xenoliths are characterized by the upper mantle rocks modified to certain extent by the enriched mantle fluid metasomatism in the mantle environment, with the enriched mantle property of Iow-degree partial melting. This constitutes the important mineralogical evidence for the petrogenesis and mineralization of alkali-rich porphyry.

  11. Assessment of concrete bridge decks with alkali silica reactions

    DEFF Research Database (Denmark)

    Eriksen, Kirsten; Jansson, Jacob; Geiker, Mette Rica


    Based on investigations of concrete from an approximately 40 years old bridge a procedure to support the management of maintenance and repair of alkali silica damaged bridges is proposed. Combined petrography and accelerated expansion testing were undertaken on cores from the Bridge at Skovdiget......, Bagsværd, Denmark to provide information on the damage condition as well as the residual reactivity of the concrete. The Danish Road Directory’s guidelines for inspection and assessment of alkali silica damaged bridges will be briefly presented, and proposed modifications will be describe...

  12. Upgrading of petroleum oil feedstocks using alkali metals and hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Gordon, John Howard


    A method of upgrading an oil feedstock by removing heteroatoms and/or one or more heavy metals from the oil feedstock composition. This method reacts the oil feedstock with an alkali metal and an upgradant hydrocarbon. The alkali metal reacts with a portion of the heteroatoms and/or one or more heavy metals to form an inorganic phase separable from the organic oil feedstock material. The upgradant hydrocarbon bonds to the oil feedstock material and increases the number of carbon atoms in the product. This increase in the number of carbon atoms of the product increases the energy value of the resulting oil feedstock.

  13. Thermal stability and oil absorption of aluminum hydroxide treated by dry modification with phosphoric acid

    Institute of Scientific and Technical Information of China (English)


    The dry modification of aluminum hydroxide powders with phosphoric acid and the effects of modification of technological conditions on thermal stability, morphology and oil absorption of aluminum hydroxide powders were investigated. The results show that the increase of mass ratio of phosphoric acid to aluminum hydroxide, the decrease of mass concentration of phosphoric acid and prolongation of mixing time are favorable to the improvement of thermal stability of aluminum hydroxide; when the mass ratio of phosphoric acid to aluminum hydroxide is 5:100, the mass concentration of phosphoric acid is 200 g/L and the mixing time is 10 min, the initial temperature of loss of crystal water in aluminum hydroxide rises from about 192.10 to 208.66 ℃2,but the dry modification results in the appearance of agglomeration and macro-aggregate in the modified powders, and the oil absorption of modified powders becomes higher than that of original aluminum hydroxide.

  14. 响应面法优化提取灰树花碱溶性多糖%Optimized extraction of alkali-soluble polysaccharide of Grifola frondosa by response surface method

    Institute of Scientific and Technical Information of China (English)

    柴丽; 侯红漫; 张公亮


    利用试验设计软件Design-Expert,通过二次回归设计得到灰树花碱提多糖提取率与料液比、提取时间、氢氧化钠浓度的回归模型,该模型能较好地预测灰树花碱提多糖的提取率.探讨了影响多糖提取率的关键因素及其相互作用,得到优化提取工艺参数∶料液比1∶66,提取时间33 min,氢氧化钠浓度0.29 mol/L.在此条件下,碱溶性多糖提取率为0.70%.%The influence of liquid-solid ratio, extraction time and sodium hydroxide concentration on extraction ratio of alkali extraction Grifola frondosa polysaccharide were studied by quadratic regression orthogonal design. These three parameters were analyzed and optimized by Design-Expert experimental software through the regression model. The optimized extraction parameters were obtained as follows: liquid-solid ratio 66 : 1, extraction time 33 min, sodium hydroxide concentration 0. 29 mol/L. Under that condition, the extraction ratio of alkali-soluble polysaccharide of Grifola frondosa reached 0. 70%.

  15. IRMPD action spectroscopy of alkali metal cation-cytosine complexes: effects of alkali metal cation size on gas phase conformation. (United States)

    Yang, Bo; Wu, R R; Polfer, N C; Berden, G; Oomens, J; Rodgers, M T


    The gas-phase structures of alkali metal cation-cytosine complexes generated by electrospray ionization are probed via infrared multiple photon dissociation (IRMPD) action spectroscopy and theoretical calculations. IRMPD action spectra of five alkali metal cation-cytosine complexes exhibit both similar and distinctive spectral features over the range of ~1000-1900 cm(-1). The IRMPD spectra of the Li(+)(cytosine), Na(+)(cytosine), and K(+)(cytosine) complexes are relatively simple but exhibit changes in the shape and shifts in the positions of several bands that correlate with the size of the alkali metal cation. The IRMPD spectra of the Rb(+)(cytosine) and Cs(+)(cytosine) complexes are much richer as distinctive new IR bands are observed, and the positions of several bands continue to shift in relation to the size of the metal cation. The measured IRMPD spectra are compared to linear IR spectra of stable low-energy tautomeric conformations calculated at the B3LYP/def2-TZVPPD level of theory to identify the conformations accessed in the experiments. These comparisons suggest that the evolution in the features in the IRMPD action spectra with the size of the metal cation, and the appearance of new bands for the larger metal cations, are the result of the variations in the intensities at which these complexes can be generated and the strength of the alkali metal cation-cytosine binding interaction, not the presence of multiple tautomeric conformations. Only a single tautomeric conformation is accessed for all five alkali metal cation-cytosine complexes, where the alkali metal cation binds to the O2 and N3 atoms of the canonical amino-oxo tautomer of cytosine, M(+)(C1).

  16. Modeling changes in biomass composition during microwave-based alkali pretreatment of switchgrass. (United States)

    Keshwani, Deepak R; Cheng, Jay J


    This study used two different approaches to model changes in biomass composition during microwave-based pretreatment of switchgrass: kinetic modeling using a time-dependent rate coefficient, and a Mamdani-type fuzzy inference system. In both modeling approaches, the dielectric loss tangent of the alkali reagent and pretreatment time were used as predictors for changes in amounts of lignin, cellulose, and xylan during the pretreatment. Training and testing data sets for development and validation of the models were obtained from pretreatment experiments conducted using 1-3% w/v NaOH (sodium hydroxide) and pretreatment times ranging from 5 to 20 min. The kinetic modeling approach for lignin and xylan gave comparable results for training and testing data sets, and the differences between the predictions and experimental values were within 2%. The kinetic modeling approach for cellulose was not as effective, and the differences were within 5-7%. The time-dependent rate coefficients of the kinetic models estimated from experimental data were consistent with the heterogeneity of individual biomass components. The Mamdani-type fuzzy inference was shown to be an effective approach to model the pretreatment process and yielded predictions with less than 2% deviation from the experimental values for lignin and with less than 3% deviation from the experimental values for cellulose and xylan. The entropies of the fuzzy outputs from the Mamdani-type fuzzy inference system were calculated to quantify the uncertainty associated with the predictions. Results indicate that there is no significant difference between the entropies associated with the predictions for lignin, cellulose, and xylan. It is anticipated that these models could be used in process simulations of bioethanol production from lignocellulosic materials.

  17. Improvement of nutritive value of acacia mangium bark by alkali treatment

    Directory of Open Access Journals (Sweden)

    Elizabeth Wina


    Full Text Available Bark, especially from Acacia mangium is a by-product from wood processing industries that commonly found in Indonesiaand in big amount will cause environmental problems. One of the alternatives to utilize bark is for animal feed. The aims of this experiment are to improve the nutritive value of bark by alkali treatments (urea and sodium hydroxide and to determine the level of substitution of elephant grass by bark. The experiment consisted of 3 in vitro studies and 1 in sacco study. In vitro studies consisted of 1 the use of urea or NaOH by wetting and incubation-method, 2 the use of different concentration of Na OH (0-4% by soaking method, 3 determination of substitution level of elephant grass by treated bark. In sacco study was conducted at 0, 6, 12, 24, 48 and 72 hours of incubation to compare the degradation of treated bark to elephant grass. The results show that urea treatment did not improve DM or OM digestibilities of bark. Soaking bark in 4% NaOH solution was more effective than wetting and incubation-method in improving in vitro digestibility. (49.26% vs19.56% for soaking and dry-method, respectively. In sacco studyl shows that treated bark had a very high solubility at 0 hour incubation but the degradation at 72 hours incubation was not significantly different from that of 0 hour incubation. The gas produced at in vitro study of treated bark was very low indicated that there was no degradation of bark at all. The level of substitution of elephant grass by treated bark up to 30% gave a non-significant digestibility value to that of 100% elephant grass. In conclusion, bark after tannin-extraction was a better feedstuff for animal feed. The soaking method in 4% NaOH solution improved the digestibility of bark significantly and the level of substitution of elephant grass by treated bark was 30%.

  18. Immobilization of laccase on hybrid layered double hydroxide

    Directory of Open Access Journals (Sweden)

    David Isidoro Camacho Córdova


    Full Text Available Crystals of Mg/Al layered double hydroxide were synthesized by alkaline precipitation and treated in an aqueous solution of glutamic acid. The glutamate ions were not intercalated into the interlayer space, but were detected in the material by Fourier transform infrared spectroscopy, suggesting that only the external surfaces of crystals were modified with glutamate ions. The resulting hybrid material was tested as a support for immobilization of the enzyme laccase (Myceliophthora thermophila. The immobilized enzyme preparation was characterized by electronic paramagnetic resonance spectroscopy and by assays of catalytic activity. The activity of the immobilized laccase was 97% of the activity in the free enzyme. Layered double hydroxide is a suitable support for use in remediation of soil studies.


    Directory of Open Access Journals (Sweden)

    Rahmi Alma Farah Adang


    Full Text Available An inadequate endodontic treatment may affect the root canal system and spread beyond its apical foramina that elicit periodontal tissue developing into abscess, granuloma and radicular cyst. Periodical lesions can be treated with non surgical endodontic treatment using calcium hydroxide dressing. This case study is reporting teeth 11 with periodical lesions and infection. Evidence of a clinical healing and radiographic assessments were followed by a non surgical endodontic therapy. Successful treatment outcome is related to the elimination of infection agents from the root canal. This can activate a stimulation zone to promote regeneration. Calcium hydroxide used as a root canal dressing may promote alkalinity at the adjacent tissue , create favourable environmental condition in which hard tissue formation can occur, interfere the bactericidal activity, increase mineralization, and induce healing.

  20. Leaching kinetics of gibbsitic bauxite with sodium hydroxide

    Directory of Open Access Journals (Sweden)

    Abdel-Aal El-Sayed A.


    Full Text Available In this paper the results of a leaching kinetics study of bauxite ore with sodium hydroxide are presented. The effect of ore particle size, sodium hydroxide concentration and reaction temperature on the Al2O3 extraction rate was determined. The results obtained showed that 99% of Al2O3 was leached out using −200+270 mesh ore particle size at a reaction temperature of 105 °C for 60 min reaction time with 250 g/L NaOH. The solid-to-liquid ratio was maintained constant at 1:20. The results indicated that leaching of bauxite is the rate controlling process. The activation energy was determined to be 46.04 kJ/mole, which was characteristic for a chemically controlled process.

  1. 40 CFR 721.4663 - Fluorinated carboxylic acid alkali metal salts. (United States)


    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Fluorinated carboxylic acid alkali... Specific Chemical Substances § 721.4663 Fluorinated carboxylic acid alkali metal salts. (a) Chemical... fluorinated carboxylic acid alkali metal salts (PMNs P-95-979/980/981) are subject to reporting under...

  2. Formation of alkali-metal nanoparticles in alkali-silicate glasses under electron irradiation and thermal processing (United States)

    Bochkareva, E. S.; Sidorov, A. I.; Ignat'ev, A. I.; Nikonorov, N. V.; Podsvirov, O. A.


    Experiments and numerical simulation show that the irradiation of alkali-containing glasses using electrons at an energy of 35 keV and the subsequent thermal processing at a temperature above the vitrification point lead to the formation of spherical metal (lithium, sodium, and potassium) nanoparticles with oxide sheaths that exhibit plasmon resonances in the visible spectral range. Glasses containing two alkali metals exhibit mutual effect of metals on the formation of nanoparticles with two compositions due to the difference of ion radii and mobilities of metal ions.

  3. Adsorption behavior of condensed phosphate on aluminum hydroxide

    Institute of Scientific and Technical Information of China (English)

    GUAN Xiao-hong; CHEN Guang-hao; SHANG Chii


    Sodium pyrophosphate(pyro-P,Na4P207),sodium tripolyphosphate(tripoly-P,NasP3010),and sodium hexametaphosphate(metaP,(NaP03)6)were selected as the model compounds of condensed phosphate to investigate the adsorption behavior of condensed phosphate on aluminum hydroxide.The adsorption was found to be endothermic and divisible into two stages:(1)fast adsorption within 1 h:and(2)slow adsorption between 1 and 24 h.The modified Freundlich model simulated the fast adsorption stage well;the slow adsorption stage was described well by the first-order kinetics.The activation energies of pyro-P,tripoly-P,and meta-P adsorption on aluminum hydroxide were determined to be 20.2,22.8 and 10.9 kJ/mol P adsorbed,respectively,in the fast adsorption stage and to be and 72.5 kJ/tool P adsorbed,respectively,in the slow adsorption stage.The adsorption increased the negative charge of the aluminum hydroxide surface.Transmission electron microscopy and energy dispersive X-ray analysis analyses provided evidence that the adsorption was not uniform on the surface and that the small crystals contfibuted more to the fast adsorption than the normal sites did.The results from X-ray fluorescence spectrometry and X-ray photoelectron spectroscopy tests also revealed the uneven adsorption of condensed phosphate as a function of the penetration depth.More condensed phosphates were adsorbed on the outer surface of aluminum hydroxide than in its inner parts.

  4. Hydrothermal Synthesis of Ni/Al Layered Double Hydroxide Nanorods


    Yun Zhao; Fenfei Xiao; Qingze Jiao


    Ni/Al layered double hydroxide (LDH) nanorods were successfully synthesized by the hydrothermal reaction. The crystal structure of the products was characterized by X-ray diffraction (XRD). The morphology of the products was observed using transmission electron microscopy (TEM) and field emission scanning electron microscopy (SEM). The influences of reaction time and pH value on the morphology of the Ni/Al LDHs were investigated. The result showed that the well-crystallized nanorods of Ni/Al ...

  5. A new mechanism for radiation damage processes in alkali halides

    NARCIS (Netherlands)

    Dubinko, V.I.; Turkin, A.A.; Vainshtein, D.I.; Hartog, H.W. den


    We present a theory of radiation damage formation in alkali halides based on a new mechanism of dislocation climb, which involves the production of VF centers (self-trapped hole neighboring a cation vacancy) as a result of the absorption of H centers of dislocation lines. We consider the evolution o

  6. Powder X-ray diffraction study af alkali alanates

    DEFF Research Database (Denmark)

    Cao, Thao; Mosegaard Arnbjerg, Lene; Jensen, Torben René

    for mobile applications, new materials with high gravimetric and volumetric storage capacity of hydrogen have to be developed. Alkali alanates are promising for hydrogen storage materials. Sodium alanate stores hydrogen reversibly at moderate conditions when catalysed with, e.g. titanium, whereas potassium...

  7. Alkali and Halogen Chemistry in Volcanic Gases on Io

    CERN Document Server

    Schaefer, L


    We use chemical equilibrium calculations to model the speciation of alkalis and halogens in volcanic gases emitted on Io. The calculations cover wide temperature (500-2000 K) and pressure (10^-6 to 10^+1 bars) ranges, which overlap the nominal conditions at Pele (T = 1760 K, P = 0.01 bars). About 230 compounds of 11 elements (O, S, Li, Na, K, Rb, Cs, F, Cl, Br, I) are considered. We predict the major alkali and halogen species in a Pele-like volcanic gas and the major alklai and halogen condensates. We also model disequilibrium chemistry of the alkalis and halogens in the volcanic plume. Based on this work and our prior modeling for Na, K, and Cl in a volcanic plume, we predict the major loss processes for the alkali halide gases are photolysis and/or condensation onto grains. On the basis of elemental abundances and photochemical lifetimes, we recommend searching for gaseous KCl, NaF, LiF, LiCl, RbF, RbCl, CsF, and CsCl around volcanic vents during eruptions. Based on abundance considerations and observation...

  8. Effect of Pozzolanic Reaction Products on Alkali-silica Reaction

    Institute of Scientific and Technical Information of China (English)

    WEI Fengyan; LAN Xianghui; LV Yinong; XU Zhongzi


    The effect of fly ash on controlling alkali-silica reaction (ASR) in simulated alkali solution was studied. The expansion of mortar bars and the content of Ca(OH)2 in cement paste cured at 80 ℃ for 91 d were measured. Transmission electron microscopy (TEM) and high-resolution transmission electron microscopy (HRTEM) were employed to study the microstructure of C-S-H. TEM/energy dispersive spectroscopy (EDS) was then used to determine the composition of C-S-H. The pore structure of the paste was analyzed by mercury intrusion porosimetry (MIP). The results show that the contents of fly ash of 30% and 45% can well inhibit ASR. And the content of Ca(OH)2 decreases with the increase of fly ash. That fly ash reacted with Ca(OH)2 to produce C-S-H with a low Ca/Si molar ratio could bind more Na+ and K+ ions, and produce a reduction in the amount of soluble alkali available for ASR. At the same time, the C-S-H produced by pozzolanic reaction converted large pores to smaller ones (gel pores smaller than 10 nm) to densify the pore structure. Perhaps that could inhibit alkali transport to aggregate for ASR.

  9. Chlor-Alkali Industry: A Laboratory Scale Approach (United States)

    Sanchez-Sanchez, C. M.; Exposito, E.; Frias-Ferrer, A.; Gonzalez-Garaia, J.; Monthiel, V.; Aldaz, A.


    A laboratory experiment for students in the last year of degree program in chemical engineering, chemistry, or industrial chemistry is presented. It models the chlor-alkali process, one of the most important industrial applications of electrochemical technology and the second largest industrial consumer of electricity after aluminium industry.

  10. Influence of temperature on alkali stress adaptation in Listeria monocytogenes (United States)

    Listeria monocytogenes cells may induce alkali stress adaptation when exposed to sublethal concentrations of alkaline cleaners and sanitizers that may be frequently used in the food processing environment. In the present study, the effect of temperature on the induction and the stability of such alk...

  11. Oxidation of Dodecanoate Intercalated Iron(II)–Iron(III) Layered Double Hydroxide to Form 2D Iron(III) (Hydr)oxide Layers

    DEFF Research Database (Denmark)

    Huang, Li‐Zhi; Ayala‐Luis, Karina B.; Fang, Liping;


    A planar trioctahedral iron(II)–iron(III) hydroxide (green rust, GR) intercalated with dodecanoate (GRC12) has been oxidized by dioxygen to produce the corresponding planar iron(III) (hydr)oxide. The formulae of GRC12 and the final iron(III) product (oxGRC12) were determined to be FeII2.00FeIII1...

  12. Application of recovered magnesium hydroxide from a flue gas desulfurization system for wastewater treatment

    Energy Technology Data Exchange (ETDEWEB)

    Bishop, P.L.; Wu, Q.; Keener, T.; Zhuang, L.A.; Gurusamy, R.; Pehkonen, S.


    Magnesium hydroxide, reclaimed from the flue gas desulfurization system (FGD) at the Zimmer Power Plant, Cincinnati, Ohio, is a weak base, in the form of either a slurry or powder. It has many potential applications for wastewater treatment. The objectives of this research are (1) to characterize the reclaimed magnesium hydroxide, e.g., purity, particle size distribution, dissolution kinetics; (2) to evaluate neutralization capacity and buffering intensity of the reclaimed magnesium hydroxide; (3) to study the efficacy of the reclaimed magnesium hydroxide for nutrient removal in wastewater treatment processes; (4) to investigate whether and how the magnesium hydroxide influences the characteristics of the activated sludge floc; (5) to determine whether magnesium hydroxide improves the anaerobic sludge digestion process and associated mechanisms; and (6) to conduct a cost-benefit analysis for the application of the reclaimed magnesium hydroxide in wastewater treatment and the possibility of marketing this product. Research results to date show that the purity of the reclaimed magnesium hydroxide depends largely on the recovery hydroxide slurry. This product proved to be very effective for wastewater neutralization, compared with other commonly used chemicals, both for its neutralization capacity and its buffering intensity. Due to its relatively low solubility in water and its particle size distribution characteristics, magnesium hydroxide behaves like a weak base, which will be very beneficial for process control. The authors also found that nitrogen and phosphorus could be removed from the wastewater using magnesium hydroxide due to their complexation and precipitation as magnesium ammonium phosphate (struvite). Magnesium hydroxide also greatly enhanced the settleability of the activated sludge. Intensive research on the mechanisms associated with these phenomena reveals that sweep flocculation and magnesium ion bridging between exopolymeric substances (EPS) of

  13. Effect of Anti-freezing Admixtures on Alkali-silica Reaction in Mortars

    Institute of Scientific and Technical Information of China (English)

    LIU Junzhe; LI Yushun; LV Lihua


    The influence of anti-freezing admixture on the alkali aggregate reaction in mortar was analyzed with accelerated methods. It is confirmed that the addition of sodium salt ingredients of anti-freezing admixture accelerates the alkali silica reaction to some extent, whereas calcium salt ingredient of anti-freezing admixture reduces the expansion of alkali silica reaction caused by high alkali cement. It is found that the addition of the fly ash considerably suppresses the expansion of alkali silica reaction induced by the anti-freezing admixtures.

  14. 利用碱提酸沉法从膨化玉米黄粉中提取谷蛋白%Extraction of gluten from extruded corn gluten meal with alkali-dissolution and acid-precipitation

    Institute of Scientific and Technical Information of China (English)

    张铁; 刘晓兰; 郑喜群


    采用碱提酸沉法提取膨化的玉米黄粉谷蛋白,选择碱液浓度、温度、料液比和浸提时间作为因素进行试验.确定最佳提取条件:碱液浓度0.55% (m/V),浸提时间100 min,温度65℃,料液比1∶16(m∶V).该条件下玉米谷蛋白的提取率为50.14%.%The method of alkali-dissolution and acid-precipitation of protein were used to extract gluten from extruded corn gluten meal. The concentration of sodium hydroxide, extracting temperature, the ratio of extruded corn gluten meal to solution of sodium hydroxide, and extracting time were investigated with test of single factor and orthogonal design of Li6(45). Optimized extraction condition were, concentration of sodium hydroxide of 0. 55% (m/V), extracting time of 100 min, temperature of 65℃ and, ratio of solid-liquid of 1 J 16. Under the optimized condition, the yield of gluten was 50. 12%,

  15. Direct ethanol fuel cell using hydrotalcite clay as a hydroxide ion conductive electrolyte. (United States)

    Tadanaga, Kiyoharu; Furukawa, Yoshihiro; Hayashi, Akitoshi; Tatsumisago, Masahiro


    An alkaline-type direct ethanol fuel cell (DEFC) using a natural clay electrolyte with non-platinum catalysts is proposed. So-called hydrotalcite clay, Mg–Al layered double hydroxide intercalated with CO₃²⁻, is shown to be a hydroxide ion conductor. An alkaline-type DEFC using this natural clay as the electrolyte and aqueous solution of ethanol and potassium hydroxide as a source of fuel exhibits excellent electrochemical performance from room temperature to 80 °C.

  16. Hydroxide ion concentration at an interface between concrete and a self-levelling flooring compound


    Anderberg, Anders; Wadsö, Lars


    This article presents results from measurements of hydroxide ion transport between a concrete and a floor screed of a lower alkalinity than the concrete. As many floor coverings and floor adhesives are sensitive to high alkaline conditions it is important to know how hydroxide ions are transported to be able to evaluate the long-term function of floor constructions. It was found that only minor transport of hydroxide ions occurs in the hygroscopic moisture range. One conclusion is therefore t...

  17. Process for carbonaceous material conversion and recovery of alkali metal catalyst constituents held by ion exchange sites in conversion residue (United States)

    Sharp, David W.


    In a coal gasification operation or similar conversion process carried out in the presence of an alkali metal-containing catalyst wherein solid particles containing alkali metal residues are produced, alkali metal constituents are recovered for the particles by contacting or washing them with an aqueous solution containing calcium or magnesium ions in an alkali metal recovery zone at a low temperature, preferably below about F. During the washing or leaching process, the calcium or magnesium ions displace alkali metal ions held by ion exchange sites in the particles thereby liberating the ions and producing an aqueous effluent containing alkali metal constituents. The aqueous effluent from the alkali metal recovery zone is then recycled to the conversion process where the alkali metal constituents serve as at least a portion of the alkali metal constituents which comprise the alkali metal-containing catalyst.

  18. Combined Effect of Water Retting and Sodium Hydroxide Concentration on Properties of Luffa Cylindrica Fibres

    Directory of Open Access Journals (Sweden)

    Charles Wetaka


    Full Text Available Luffa cylindrica is an annual climbing plant whose fruit has a vascular network of fibres. These fibres are held together by pectins which degrade during water retting to release the fibres. In this paper, the extraction of luffa cylindrica fibres together with the combined effect of water retting and alkali treatment on its tensile properties are reported. The fibres were extracted from mature fruits of Luffa cylindrica through aerobic water retting process over a duration of 2 weeks, 4 weeks and 8 weeks. The extracted fibres were oven dried to a moisture content of 9.74±1.1% and tested in tension at gauge lengths of 10 mm. The fibres were characterized in terms of moisture regain, lignin content, hemicellulose content, and cellulose content. The combined effect of water retting and sodium hydroxide (NaOH concentration on the fibre’s breaking load, elongation, tenacity and linear density was also investigated. The luffa cylindrica fibres had a moisture regain of 10.81%, lignin content of 12.03%, cellulose content of 65.69%, and hemicellulose content of 19%. The linear density of the fibres retted for 2-8 weeks was 572–470 dTex .The determined breaking load of the fibres retted for 2-8 weeks was 1444.19-417.04 cN and 997.81-298.05 cN after treatments with 0% -16% NaOH. The fibre elongation was 4.0-24% after 2-8 weeks of retting and 4.3-14.5 % after treatments with 0% -16% NaOH. Tenacity of luffa cylindrica fibres was 6.0-25.25 cN/Tex after 2-8 weeks of retting and 5.9-20.22 cN/Tex after treatments with 0% -16% NaOH. From the study, an increase in aerobic water retting and concentration of NaOH had a positive effect on the tensile properties of the luffa cylindrica fibres.

  19. Antimicrobial activity of calcium hydroxide and chlorhexidine on intratubular Candida albicans

    Institute of Scientific and Technical Information of China (English)

    Ronan Jacques Rezende Delgado; Thaís Helena Gasparoto; Carla Renata Sipert; Claudia Ramos Pinheiro; Ivaldo Gomes de Moraes; Roberto Brandāo Garcia; Marco Antonio Hungaro Duarte; Clóvis Monteiro Bramante; Sérgio Aparecido Torres; Gustavo Pompermaier Garlet; Ana Paula Campanelli; Norberti Bernardineli


    This study investigated the efficacy of calcium hydroxide and chlorhexidine gel for the elimination of intratubular Candida albicans (C. albicans). Human single-rooted teeth contaminated with C. albicans were treated with calcium hydroxide, 2% chlorhexidine gel, calcium hydroxide plus 2% chlorhexidine gel, or saline (0.9% sodium chloride) as a positive control. The samples obtained at depths of 0-100 and 100-200 μm from the root canal system were analyzed for C. albicans load by counting the number of colony forming units and for the percentage of viable C. albicans using fluorescence microscopy. First, the antimicrobial activity of calcium hydroxide and the 2% chlorhexidine gel was evaluated by counting the number of colony forming units. After 14 days of intracanal medication, there was a significant decrease in the number of C. albicanscolony forming units at a depth of 0-100 lzm with chlorhexidine treatment either with or without calcium hydroxide compared with the calcium hydroxide only treatment. However, there were no differences in the number of colony forming units at the 100-200 μm depth for any of the medications investigated. C. albicans viability was also evaluated by vital staining techniques and fluorescence microscopy analysis. Antifungal activity against C. albicans significantly increased at both depths in the chlorhexidine groups with and without calcium hydroxide compared with the groups treated with calcium hydroxide only. Treatments with only chlorhexidine or chlorhexidine in combination with calcium hydroxide were effective for elimination of C. albicans.

  20. Effects of salinity and humic acid on the sorption of Hg on Fe and Mn hydroxides. (United States)

    Liang, Peng; Li, Yi-Chun; Zhang, Chan; Wu, Sheng-Chun; Cui, Hao-Jie; Yu, Shen; Wong, Ming H


    The objective of this study was to investigate the influence of humic acid (HA) and salinity on adsorption of Hg on the amorphous and crystalline of iron and manganese hydroxides. The results show that the adsorption of Hg(2+) on Fe and Mn hydroxides was inhibited in marine system due to the formation of stable, nonsorbing aqueous HgCl(2) complexes in solution. Moreover, Cl(-) inhibited the Hg(2+) adsorption more severely on amorphous than crystalline hydroxides. The addition of HA inhibited Hg(2+) adsorption on Fe and Mn hydroxides in freshwater system might be attributed to the competition between Hg(2+) and HA on adsorption to Fe and Mn hydroxides. In contrast, the addition of HA promoted Hg(2+) adsorption on Fe and Mn hydroxides in the marine system, which might be due to the addition of humic acid resulted in the reaction between Cl(-) and HA, and therefore the reducing of Cl(-) promoted more Hg(2+) on Fe and Mn hydroxides. In addition, the influence of HA on Hg(2+) adsorption on Fe and Mn hydroxides are more visible for crystalline than amorphous hydroxides.

  1. Effective Production of Sorbitol and Mannitol from Sugars Catalyzed by Ni Nanoparticles Supported on Aluminium Hydroxide


    Rodiansono Rodiansono; Shimazu Shogo


    Effective production of hexitols (sorbitol and mannitol) was achieved from sugars by means of nickel nanoparticles supported on aluminium hydroxide (NiNPs/AlOH) catalyst. NiNPs/AlOH catalyst was prepared by a simple and benign environmentally procedure using less amount of sodium hydroxide. ICP-AES and XRD analyses confirmed that the NiNPs/AlOH catalysts comprised a large amount of remained aluminium hydroxide (i.e. bayerite and gibbsite). The presence of aluminium hydroxide caused a high dis...

  2. Generation and characterization of alkali metal clusters in Y-FAU zeolites. An ESR and MAS NMR spectroscopic study (United States)

    Hannus, István; Béres, Attila; Nagy, János B.; Halász, János; Kiricsi, Imre


    Charged and neutral metal clusters of various compositions and sizes can be prepared by controlling the alkali metal content by the decomposition of alkali azides and the composition of the host zeolite by ion-exchange. ESR signals show that electron transfer from alkali metal atoms to alkali metal cations does occur, but in a direction opposite to that predicted by the gas-phase thermochemistry. Alkali metal clusters proved to be very active basic catalytic centers.

  3. Kinetics of sorption of oil products by hydroxide precipitates

    Energy Technology Data Exchange (ETDEWEB)

    Petrova, N.A.; Dubrovskaya, G.E.; Berezyuk, V.G.; Pushkarev, V.V.


    Study of the kinetics of sorption of oils (palm and coriander oils, Genrex-26, Emulsol E-2(B)) under static conditions by aluminum and iron hydroxide precipitates (with FeSO/sub 4/, FeCl/sub 3/, and AlCl/sub 3/ as coagulants) showed that an increase of temperature to 40 to 50/sup 0/C raises the sorption rate substantially. The kinetic relations can be represented by equations for first-order reactions. The calculated rate constants and the values of the empirical activation energies are evidence of physical sorption with diffusion as the controlling step.

  4. Kinetics of gibbsite leaching in sodium hydroxide aqueous solution

    Directory of Open Access Journals (Sweden)

    Pavlović Ljubica J.


    Full Text Available In order to study the kinetics and mechanism of the reaction, laboratory leaching was carried out with industrially produced gibbsite γ-Al(OH3 in aqueous solutions containing an excess of sodium hydroxide. The results obtained reaction temperature, duration and base concentration varied. The basic kinetic parameters were determined from: the reaction rate constant k=8.72·107 exp (-74990/RT and the process activation energy in the range Ea=72.5-96.81 kJ/mol.

  5. The photoluminescence of Co-Al-layered double hydroxide

    Institute of Scientific and Technical Information of China (English)


    We report a new optical behaviour of pure Co-Al-layered double hydroxide (LDH). It was found that the Co-Al-LDH sample could emit fluorescence without any fluorescent substances intercalated. Its excitation spectrum shows a maximum peak near the wavelength 370 nm, the maximum emission peak appears at 430 nm and the photoluminescence colour of the Co-Al-LDH sample is blue. This new optical property will be expected to extend the potential applications of LDHs in optical materials field.


    Directory of Open Access Journals (Sweden)

    Luíz Paulo Figueredo Benício


    Full Text Available The current research aims to introduce Layered Double Hydroxides (LDH as nanomaterials to be used in agriculture, with particular reference to its use as storage and slow release matrix of nutrients and agrochemicals for plant growing. Structural characteristics, main properties, synthesis methods and characterization of LDH were covered in this study. Moreover, some literature data have been reported to demonstrate their potential for storage and slow release of nitrate, phosphate, agrochemicals, besides as being used as adsorbent for the wastewater treatment. This research aims to expand, in near future, the investigation field on these materials, with application in agriculture, increasing the interface between chemistry and agronomy.

  7. Coherent coupling of alkali atoms by random collisions

    CERN Document Server

    Katz, Or; Firstenberg, Ofer


    Random spin-exchange collisions in warm alkali vapor cause rapid decoherence and act to equilibriate the spin state of the atoms. In contrast, here we demonstrate experimentally and theoretically a coherent coupling of one alkali specie to another specie, mediated by these random collisions. We show that, the minor specie (potassium) inherits the magnetic properties of the dominant specie (rubidium), including its lifetime (T1), coherence time (T2), gyromagnetic ratio, and SERF magnetic-field threshold. We further show that this coupling can be completely controlled by varying the strength of the magnetic field. Finally, we explain these phenomena analytically by modes-mixing of the two species via spin-exchange collisions.

  8. Alkali-helium snowball complexes formed on helium nanodroplets. (United States)

    Müller, S; Mudrich, M; Stienkemeier, F


    We systematically investigate the formation and stability of snowballs formed by femtosecond photoionization of small alkali clusters bound to helium nanodroplets. For all studied alkali species Ak = (Na,K,Rb,Cs) we observe the formation of snowballs Ak(+)He(N) when multiply doping the droplets. Fragmentation of clusters Ak(N) upon ionization appears to enhance snowball formation. In the case of Na and Cs we also detect snowballs Ak(2) (+)He(N) formed around Ak dimer ions. While the snowball progression for Na and K is limited to less than 11 helium atoms, the heavier atoms Rb and Cs feature wide distributions at least up to Ak(+)He(41). Characteristic steps in the mass spectra of Cs-doped helium droplets are found at positions consistent with predictions on the closure of the first shell of helium atoms around the Ak(+) ion based on variational Monte Carlo simulations.

  9. Coherent coupling of alkali atoms by random collisions. (United States)

    Katz, Or; Peleg, Or; Firstenberg, Ofer


    Random spin-exchange collisions in warm alkali vapor cause rapid decoherence and act to equilibrate the spin state of the atoms in the vapor. In contrast, here we demonstrate experimentally and theoretically a coherent coupling of one alkali species to another species, mediated by these random collisions. We show that the minor species (potassium) inherits the magnetic properties of the dominant species (rubidium), including its lifetime (T_{1}), coherence time (T_{2}), gyromagnetic ratio, and spin-exchange relaxation-free magnetic-field threshold. We further show that this coupling can be completely controlled by varying the strength of the magnetic field. Finally, we explain these phenomena analytically by mode mixing of the two species via spin-exchange collisions.

  10. Penetration of alkali atoms throughout a graphene membrane: theoretical modeling. (United States)

    Boukhvalov, D W; Virojanadara, C


    Theoretical studies of penetration of various alkali atoms (Li, Na, Rb, Cs) throughout a graphene membrane grown on a silicon carbide substrate are reported and compared with recent experimental results. Results of first principles modeling demonstrate a rather low (about 0.8 eV) energy barrier for the formation of temporary defects in the carbon layer required for the penetration of Li at a high concentration of adatoms, a higher (about 2 eV) barrier for Na, and barriers above 4 eV for Rb and Cs. Experiments prove migration of lithium adatoms from the graphene surface to the buffer layer and SiC substrate at room temperature, sodium at 100 °C and impenetrability of the graphene membrane for Rb and Cs. Differences between epitaxial and free-standing graphene for the penetration of alkali ions are also discussed.

  11. The optical properties of alkali nitrate single crystals (United States)

    Anan'ev, Vladimir; Miklin, Mikhail


    Absorption of non-polarized light by a uniaxial crystal has been studied. The degree of absorption polarization has been calculated as a function of the ratio of optical densities in the region of low and high absorbances. This function is proposed for analysis of the qualitative and quantitative characteristics of uniaxial crystal absorption spectra. Non-polarized light spectra of alkali nitrate single crystals, both pure and doped with thallium, have been studied. It is shown that the absorption band at 300 nm is due to two transitions, whose intensities depend on temperature in various ways. There is a weak band in a short wavelength range of the absorption spectrum of potassium nitrate crystal, whose intensity increases with thallium doping. The band parameters of alkali nitrate single crystals have been calculated. Low-energy transitions in the nitrate ion have been located.

  12. Polarizabilities and hyperpolarizabilities of the alkali metal atoms

    Energy Technology Data Exchange (ETDEWEB)

    Fuentealba, P. (Chile Univ., Santiago (Chile). Departamento de Fisica and Centro de Mecanica Cuantica Aplicada (CMCA)); Reyes, O. (Chile Univ., Santiago (Chile). Dept. de Fisica)


    The electric static dipole polarizability [alpha], quadrupole polarizability C, dipole-quadrupole polarizability B, and the second dipole hyperpolarizability [gamma] have been calculated for the alkali metal atoms in the ground state. The results are based on a pseudopotential which is able to incorporate the very important core-valence correlation effect through a core polarization potential, and, in an empirical way, the main relativistic effects. The calculated properties compare very well with more elaborated calculations for the Li atom, excepting the second hyperpolarizability [gamma]. For the other atoms, there is neither theoretical nor experimental information about most of the higher polarizabilities. Hence, the results of this paper should be seen as a first attempt to give a complete account of the series expansion of the interaction energy of an alkali metal atom and a static electric field. (author).

  13. Density functional study of ferromagnetism in alkali metal thin films

    Indian Academy of Sciences (India)

    Prasenjit Sen


    Electronic and magnetic structures of (1 0 0) films of K and Cs, having thicknesses of one to seven layers, are calculated within the plane-wave projector augmented wave (PAW) formalism of the density functional theory (DFT), using both local spin density approximation (LSDA) and the PW91 generalized gradient approximation (GGA). Only a six-layer Cs film is found to have a ferromagnetic (FM) state which is degenerate with a paramagnetic (PM) state within the accuracy of these calculations. These results are compared with those obtained from calculations on a finite-thickness uniform jellium model (UJM), and it is argued that within LSDA or GGA, alkali metal thin films cannot be claimed to have an FM ground state. Relevance of these results to the experiments on transition metal-doped alkali metal thin films and bulk hosts are also discussed.


    Institute of Scientific and Technical Information of China (English)

    郝冬梅; 王新灵; 朱卫华; 唐小真; 刘成岑; 施凯


    Hollow polymer latex particles were prepared by seeded emulsion polymerization. A seed latex consisting of styrene (St), butyl acrylate(BA) copolymer was first prepared, and seeded terpolymerization of St-BA-MA(methacrylic acid) were then carried out in the absence of surfactant. Final latex was treated by a two-step treatment under alkaline and acidic conditions, thus, the particles with hollow structure were obtained. We discussed the effects of pH value, temperature and time in alkali and acid treatment processes on hollow structure within the polymer latex particles and amount of carboxylic group on particle surface. The results show that the hollow polymer latex particles with the largest hollow size can be obtained under a certain condition (pH12.5, 90°C, 3 h in alkali treatment stage and pH2.5, 85°C, 3 h in acid treatment stage).

  15. Alkali halide microstructured optical fiber for X-ray detection

    Energy Technology Data Exchange (ETDEWEB)

    DeHaven, S. L., E-mail:, E-mail:; Wincheski, R. A., E-mail:, E-mail: [NASA Langley Research Center, Hampton, VA 23681 (United States); Albin, S., E-mail: [Norfolk State University, Norfolk, VA 23504 (United States)


    Microstructured optical fibers containing alkali halide scintillation materials of CsI(Na), CsI(Tl), and NaI(Tl) are presented. The scintillation materials are grown inside the microstructured fibers using a modified Bridgman-Stockbarger technique. The x-ray photon counts of these fibers, with and without an aluminum film coating are compared to the output of a collimated CdTe solid state detector over an energy range from 10 to 40 keV. The photon count results show significant variations in the fiber output based on the materials. The alkali halide fiber output can exceed that of the CdTe detector, dependent upon photon counter efficiency and fiber configuration. The results and associated materials difference are discussed.

  16. Positronium-alkali atom scattering at medium energies

    Energy Technology Data Exchange (ETDEWEB)

    Chakraborty, Ajoy [Laban Hrad Vidyapith, AD-369, Salt Lake City, Kolkata 700 064 (India); Basu, Arindam [Department of Physics, Maheshtala College, Chandannagar, South 24 Parganas, Kolkata 700 140 (India); Sarkar, Nirmal K [Sodepur Chandrachur Vidyapith, 1, Desh Bandhu Nagar, Sodepur, 743 174 (India); Sinha, Prabal K [Department of Physics, Bangabasi College, 19, Raj Kumar Chakravorty Sarani, Kolkata 700 009 (India)


    We investigate the scattering of orthopositronium (o-Ps) atom off different atomic alkali targets (Na to Cs) at low and medium energies (up to 120 eV). Projectile-elastic and target-elastic close-coupling models have been employed to investigate the systems in addition to the static-exchange model. Elastic, excitation and total cross sections have been reported for all four systems. The magnitude of the alkali excitation cross section increases with increasing atomic number of the target atom while the position of the peak value shifts towards lower incident energies. The magnitudes of the Ps excitation and ionization cross sections increase steadily with atomic number with no change in the peak position. The reported results show regular behaviour with increasing atomic number of the target atom. Scattering parameters for the Ps-Rb and Ps-Cs systems are being reported for the first time.

  17. Alkali Halide Microstructured Optical Fiber for X-Ray Detection (United States)

    DeHaven, S. L.; Wincheski, R. A.; Albin, S.


    Microstructured optical fibers containing alkali halide scintillation materials of CsI(Na), CsI(Tl), and NaI(Tl) are presented. The scintillation materials are grown inside the microstructured fibers using a modified Bridgman-Stockbarger technique. The x-ray photon counts of these fibers, with and without an aluminum film coating are compared to the output of a collimated CdTe solid state detector over an energy range from 10 to 40 keV. The photon count results show significant variations in the fiber output based on the materials. The alkali halide fiber output can exceed that of the CdTe detector, dependent upon photon counter efficiency and fiber configuration. The results and associated materials difference are discussed.

  18. Solubility of 1:1 Alkali Nitrates and Chlorides in Near-Critical and Supercritical Water : 1 Alkali Nitrates and Chlorides in Near-Critical and Supercritical Water

    NARCIS (Netherlands)

    Leusbrock, Ingo; Metz, Sybrand J.; Rexwinkel, Glenn; Versteeg, Geert F.


    To increase the available data oil systems containing supercritical water and inorganic compounds, all experimental setup was designed to investigate the solubilities of inorganic compounds Ill supercritical water, In this work, three alkali chloride salts (LiCl, NaCl, KCl) and three alkali nitrate

  19. A hidden history of heartburn: The milk-alkali syndrome



    Milk-alkali syndrome was once considered to be of historic interest and a rare cause of hypercalcemia. Currently, it should be an important consideration in the differential diagnosis of hypercalcemia, after malignancies and primary hyperparathyroidism. The resurgence is in part due to the easy availability of over the counter (OTC) calcium preparations. We describe a 50-year-old man who presented with severe hypercalcemia on two occasions associated with renal failure and metabolic alkalosis...

  20. Efficient potassium diode pumped alkali laser operating in pulsed mode. (United States)

    Zhdanov, Boris V; Rotondaro, Matthew D; Shaffer, Michael K; Knize, Randall J


    This paper presents the results of our experiments on the development of an efficient hydrocarbon free diode pumped alkali laser based on potassium vapor buffered by He gas at 600 Torr. A slope efficiency of more than 50% was demonstrated with a total optical conversion efficiency of 30%. This result was achieved by using a narrowband diode laser stack as the pump source. The stack was operated in pulsed mode to avoid limiting thermal effects and ionization.

  1. Composition and thermodynamic properties of dense alkali metal plasmas

    Energy Technology Data Exchange (ETDEWEB)

    Gabdullin, M.T. [NNLOT, al-Farabi Kazakh National University, 71 al-Farabi Str., Almaty 050035 (Kazakhstan); Ramazanov, T.S.; Dzhumagulova, K.N. [IETP, al-Farabi Kazakh National University, 71 al-Farabi Str., Almaty 050035 (Kazakhstan)


    In this work composition and thermodynamic properties of dense alkali metal plasmas (Li, Na) were investigated. Composition was derived by solving the Saha equations with corrections due to nonideality. The lowering of the ionization potentials was calculated on the basis of pseudopotentials by taking screening and quantum effects into account (copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  2. Engineering Properties of Alkali-Activated Fly Ash Concrete



    This paper reports the results of experimental research on certain engineering properties of a new (portland cement-free) concrete made with alkali-activated fly ash. Laboratory tests were conducted to determine its (bending and compression) mechanical strength, modulus of elasticity, bond strength, and shrinkage. The results show that mortar and concrete made with portland cement-free activated fly ash develop a high mechanical strength in short periods of time, have a moderate modulus of el...

  3. Ultrafine microporous and mesoporous activated carbon fibers from alkali lignin



    A facile and sustainable approach has been successfully devised to fabricate ultrafine (100-500 nm) highly porous activated carbon fibers (ACFs) by electrospinning of aqueous solutions of predominantly alkali lignin (low sulfonate content) followed by simultaneous carbonization and activation at 850 °C under N2. Incorporating a polyethylene oxide (PEO) carrier with only up to one ninth of lignin not only enabled efficient electrospinning into fibers but also retained fibrous structures during...

  4. On-line alkali monitoring - Part 1; Kontinuerlig alkalimaetning - Etapp 1

    Energy Technology Data Exchange (ETDEWEB)

    Andersson, Christer; Ljung, P.; Woxlin, H.


    As a consequence of the increased knowledge of the environmental impact of combustion based heat and power generation, the use of renewable biofuels will be increased. An obstacle associated to biofuel combustion compared to other fuels is the large release of alkali. Alkali compounds in flue gases are known to cause severe operational problems. Three of the major problems are; fouling of superheating tubes (causing reduced heat transfer and possibly corrosion), agglomeration of the bed material in fluidized beds, and poisoning of SCR catalysts. Yet another alkali related problem arises when, in order to increase the electric efficiency of combustion power plants, combined-cycle technology is used. Alkali vapour present in the fuel gas for the gas turbine is condensed to particles which increase corrosion and erosion of the turbine blades. The research on ash related operational problems has to be extended in order to ensure future use of biofuels in heat and power generation. In all successful research, adequate tools are necessary. To investigate ash related problems the key issue is to be able to perform continuous alkali measurements. This pilot study has investigated the need of continuous alkali measurements, which alkali species are harmful in the different applications and also available instrumentation capable of measuring the specific alkali species. The report gives a short summary presenting alkali related operational problems. In addition a schematic overview is given, showing the alkali species that possibly can exist in various parts of the power plant. 48 refs, 13 figs, 4 tabs

  5. The unexpected properties of alkali metal iron selenide superconductors

    Energy Technology Data Exchange (ETDEWEB)

    Dagotto, Elbio R [ORNL


    The iron-based superconductors that contain FeAs layers as the fundamental building block in the crystal structures have been rationalized in the past using ideas based on the Fermi surface nesting of hole and electron pockets when in the presence of weak Hubbard U interactions. This approach seemed appropriate considering the small values of the magnetic moments in the parent compounds and the clear evidence based on photoemission experiments of the required electron and hole pockets. However, recent results in the context of alkali metal iron selenides, with generic chemical composition AxFe2ySe2 (A alkali metal element), have challenged those previous ideas since at particular compositions y the low-temperature ground states are insulating and display antiferromagnetic order with large iron magnetic moments. Moreover, angle-resolved photoemission studies have revealed the absence of hole pockets at the Fermi level in these materials. The present status of this exciting area of research, with the potential to alter conceptually our understanding of the ironbased superconductors, is here reviewed, covering both experimental and theoretical investigations. Other recent related developments are also briefly reviewed, such as the study of selenide two-leg ladders and the discovery of superconductivity in a single layer of FeSe. The conceptual issues considered established for the alkali metal iron selenides, as well as several issues that still require further work, are discussed.

  6. Scattering of positrons and electrons by alkali atoms (United States)

    Stein, T. S.; Kauppila, W. E.; Kwan, C. K.; Lukaszew, R. A.; Parikh, S. P.; Wan, Y. J.; Zhou, S.; Dababneh, M. S.


    Absolute total scattering cross sections (Q sub T's) were measured for positrons and electrons colliding with sodium, potassium, and rubidium in the 1 to 102 eV range, using the same apparatus and experimental approach (a beam transmission technique) for both projectiles. The present results for positron-sodium and -rubidium collisions represent the first Q sub T measurements reported for these collision systems. Features which distinguish the present comparisons between positron- and electron-alkali atom Q sub T's from those for other atoms and molecules (room-temperature gases) which have been used as targets for positrons and electrons are the proximity of the corresponding positron- and electron-alkali atom Q sub T's over the entire energy range of overlap, with an indication of a merging or near-merging of the corresponding positron and electron Q sub T's near (and above) the relatively low energy of about 40 eV, and a general tendency for the positron-alkali atom Q sub T's to be higher than the corresponding electron values as the projectile energy is decreased below about 40 eV.

  7. Plasma formation in diode pumped alkali lasers sustained in Cs (United States)

    Markosyan, Aram H.; Kushner, Mark J.


    In diode pumped alkali lasers (DPALs), lasing action occurs on the resonant lines of alkali atoms following pumping by broadband semiconductor lasers. The goal is to convert the efficient but usually poor optical quality of inexpensive diode lasers into the high optical quality of atomic vapor lasers. Resonant excitation of alkali vapor leads to plasma formation through the excitation transfer from the 2P states to upper lying states, which then are photoionized by the pump and intracavity radiation. A first principles global model was developed to investigate the operation of the He/Cs DPAL system and the consequences of plasma formation on the efficiency of the laser. Over a range of pump powers, cell temperatures, excitation frequency, and mole fraction of the collision mixing agent (N2 or C2H6), we found that sufficient plasma formation can occur that the Cs vapor is depleted. Although N2 is not a favored collisional mixing agent due to large rates of quenching of the 2P states, we found a range of pump parameters where laser oscillation may occur. The poor performance of N2 buffered systems may be explained in part by plasma formation. We found that during the operation of the DPAL system with N2 as the collisional mixing agent, plasma formation is in excess of 1014-1015 cm-3, which can degrade laser output intensity by both depletion of the neutral vapor and electron collisional mixing of the laser levels.

  8. Heterometallic aluminates: alkali metals trapped by an aluminium aryloxide claw. (United States)

    Muñoz, M Teresa; Cuenca, Tomás; Mosquera, Marta E G


    A series of heterometallic aluminium-alkali metal species [AlMMe2{2,6-(MeO)2C6H3O}2]n have been isolated for lithium, sodium and potassium. These compounds can be generated by the reaction of [AlMe2{2,6-(MeO)2C6H3O}]2 with the metallated phenol [M{2,6-(MeO)2C6H3O}]n or through the reaction of the mixture of AlMe3 and the appropriate alkali metal alkyl base with two equivalents of 2,6-dimethoxyphenol. In the heterometallic species obtained, the {AlMe2{2,6-(MeO)2C6H3O}2}(-) moiety is observed and could be described as a claw which fixes the alkali ion by the phenoxide oxygen atoms while the methoxy groups help to stabilize their coordination sphere. All compounds have been characterized by NMR spectroscopy and X-ray diffraction methods. Catalytic studies reveal that these compounds are active in ring-opening polymerization of L-lactide.

  9. Electron densities and alkali atoms in exoplanet atmospheres

    Energy Technology Data Exchange (ETDEWEB)

    Lavvas, P. [GSMA, Université de Reims Champagne Ardenne, CNRS UMR 7331, Reims, 51687 France (France); Koskinen, T.; Yelle, R. V., E-mail: [Lunar and Planetary Laboratory, University of Arizona, Tucson, AZ 85719 (United States)


    We describe a detailed study on the properties of alkali atoms in extrasolar giant planets, and specifically focus on their role in generating the atmospheric free electron densities, as well as their impact on the transit depth observations. We focus our study on the case of HD 209458b, and we show that photoionization produces a large electron density in the middle atmosphere that is about two orders of magnitude larger than the density anticipated from thermal ionization. Our purely photochemical calculations, though, result in a much larger transit depth for K than observed for this planet. This result does not change even if the roles of molecular chemistry and excited state chemistry are considered for the alkali atoms. In contrast, the model results for the case of exoplanet XO-2b are in good agreement with the available observations. Given these results we discuss other possible scenarios, such as changes in the elemental abundances, changes in the temperature profiles, and the possible presence of clouds, which could potentially explain the observed HD 209458b alkali properties. We find that most of these scenarios cannot explain the observations, with the exception of a heterogeneous source (i.e., clouds or aerosols) under specific conditions, but we also note the discrepancies among the available observations.

  10. Superconductivity in alkali-doped C{sub 60}

    Energy Technology Data Exchange (ETDEWEB)

    Ramirez, Arthur P., E-mail:


    Highlight: • Superconductivity in alkali-doped C{sub 60} (A{sub 3}C{sub 60}) is well described by an s-wave state produced by phonon mediated pairing. • Moderate coupling of electrons to high-frequency shape-changing intra-molecular vibrational modes produces transition temperatures up to 33 K in single-phase material. • The good understanding of pairing in A{sub 3}C{sub 60} offers a paradigm for the development of new superconducting materials. - Abstract: Superconductivity in alkali-doped C{sub 60} (A{sub 3}C{sub 60}, A = an alkali atom) is well described by an s-wave state produced by phonon mediated pairing. Moderate coupling of electrons to high-frequency shape-changing intra-molecular vibrational modes produces transition temperatures (T{sub c}) up to 33 K in single-phase material. The good understanding of pairing in A{sub 3}C{sub 60} offers a paradigm for the development of new superconducting materials.

  11. Selectivity of Crystal Growth Direction in Layered Double Hydroxides

    Institute of Scientific and Technical Information of China (English)

    赵芸; 梁吉; 李峰; 段雪


    Investigation of selectivity of crystal growth direction in layered double hydroxides is helpful to control their particle sizes in different directions. Mg-Al layered double hydroxides (LDHs) were synthesized using a coprecipitation method. The influences of aging temperature, aging time, and Mg/Al molar ratio on the crystal structure, the LDHs particle size, and the selectivity of crystal growth in different directions were investigated. The results show that the size of the crystallites in the a direction is larger than that in the c direction for all experimental conditions, indicating faster crystal growth in the a direction than in the c direction. The crystallite sizes in the a and c directions both increase with decreasing Mg/Al molar ratio but with less difference between the sizes in the two directions. Therefore, the crystal growth rate in the c direction increases more than that in the a direction as the Mg/Al molar ratio decreases. The influence of the aging time, aging temperature, and Mg/Al molar ratio on the selectivity of the crystal growth direction can be used to prepare LDHs with selected sizes in the a and c directions.

  12. Experimental and Theoretical Studies of Volatile Metal Hydroxides (United States)

    Myers, Dwight L.; Jacobson, Nathan S.


    Modern superalloys used in the construction of turbomachinery contain a wide range of metals in trace quantities. In addition, metal oxides and silicon dioxide are used to form Thermal Barrier Coatings (TBC) to protect the underlying metal in turbine blades. Formation of volatile hydroxides at elevated temperatures is an important mechanism for corrosion of metal alloys or oxides in combustion environments (N. Jacobson, D. Myers, E. Opila, and E. Copland, J. Phys. Chem. Solids 66, 471-478, 2005). Thermodynamic data is essential to proper design of components of modern gas turbines. It is necessary to first establish the identity of volatile hydroxides formed from the reaction of a given system with high temperature water vapor, and then to determine the equilibrium pressures of the species under operating conditions. Theoretical calculations of reaction energies are an important check of experimental results. This presentation reports results for several important systems: Si-O-H, Cr-O-H, Al-O-H, Ti-O-H, and ongoing studies of Ta-O-H.

  13. Cation ordering and superstructures in natural layered double hydroxides. (United States)

    Krivovichev, Sergey V; Yakovenchuk, Victor N; Zolotarev, Andrey A; Ivanyuk, Gregory N; Pakhomovsky, Yakov A


    Layered double hydroxides (LDHs) constitute an important group of materials with many applications ranging from catalysis and absorption to carriers for drug delivery, DNA intercalation and carbon dioxide sequestration. The structures of LDHs are based upon double brucite-like hydroxide layers [M(2+)(n)M(3+)(m)(OH)(2(m+n)](m+), where M(2+) = Mg(2+), Fe(2+), Mn(2+), Zn(2+), etc.; M(3+) = Al(3+), Fe(3+), Cr(3+), Mn(3+), etc. Structural features of LDHs such as cation ordering, charge distribution and polytypism have an immediate influence upon their properties. However, all the structural studies on synthetic LDHs deal with powder samples that prevent elucidation of such fine details of structure architecture as formation of superstructures due to cation ordering. In contrast to synthetic materials, natural LDHs are known to form single crystals accessible to single-crystal X-ray diffraction analysis, which provides a unique possibility to investigate 3D cation ordering in LDHs that results in formation of complex superstructures, where 2D cation order is combined with a specific order of layer stacking (polytypism). Therefore LDH minerals provide an indispensable source of structural information for modeling of structures and processes happening in LDHs at the molecular and nanoscale levels.

  14. Alkali metal cation-hexacyclen complexes: effects of alkali metal cation size on the structure and binding energy. (United States)

    Austin, C A; Rodgers, M T


    Threshold collision-induced dissociation (CID) of alkali metal cation-hexacyclen (ha18C6) complexes, M(+)(ha18C6), with xenon is studied using guided ion beam tandem mass spectrometry techniques. The alkali metal cations examined here include: Na(+), K(+), Rb(+), and Cs(+). In all cases, M(+) is the only product observed, corresponding to endothermic loss of the intact ha18C6 ligand. The cross-section thresholds are analyzed to extract zero and 298 K M(+)-ha18C6 bond dissociation energies (BDEs) after properly accounting for the effects of multiple M(+)(ha18C6)-Xe collisions, the kinetic and internal energy distributions of the M(+)(ha18C6) and Xe reactants, and the lifetimes for dissociation of the activated M(+)(ha18C6) complexes. Ab initio and density functional theory calculations are used to determine the structures of ha18C6 and the M(+)(ha18C6) complexes, provide molecular constants necessary for the thermodynamic analysis of the energy-resolved CID data, and theoretical estimates for the M(+)-ha18C6 BDEs. Calculations using a polarizable continuum model are also performed to examine solvent effects on the binding. In the absence of solvent, the M(+)-ha18C6 BDEs decrease as the size of the alkali metal cation increases, consistent with the noncovalent nature of the binding in these complexes. However, in the presence of solvent, the ha18C6 ligand exhibits selectivity for K(+) over the other alkali metal cations. The M(+)(ha18C6) structures and BDEs are compared to those previously reported for the analogous M(+)(18-crown-6) and M(+)(cyclen) complexes to examine the effects of the nature of the donor atom (N versus O) and the number donor atoms (six vs four) on the nature and strength of binding.

  15. Alternative alkali resistant deNO{sub x} technologies

    Energy Technology Data Exchange (ETDEWEB)

    Buus Kristensen, S.; Due-Hansen, J.; Putluru, S.S.R.; Kunov-Kruse, A.; Fehrmann, R.; Degn Jensen, A.


    The aim of the project is to identify, make and test possible alkali resistant deNO{sub x} catalysts for use in biomass, waste or fossil fuelled power plants, where the flue gas typically has a high level of potassium compounds, which rapidly de-activate the traditional V{sub 2}O{sub 5}/TiO{sub 2} catalyst. Furthermore, new technologies are investigated based on a protective coating of the catalyst elements and selective reversible absorption of NO{sub x} with ionic liquids. Several promising alternative deNO{sub x} catalyst types have been made during the project: 1) V, Fe, CU based nano-TiO{sub 2} and nano-TiO{sub 2}-SO{sub 4}{sup 2-} catalysts; 2) V/ZrO{sub 2}-SO{sub 2}- and V/ZrO{sub 2}-CeO{sub 2} catalysts; V, Fe, Cu based Zeolite catalysts; 4) V, Fe, Cu based Heteropoly acid catalysts. Several of these are promising alternatives to the state-of the art industrial reference catalyst. All catalysts prepared in the present project exhibit higher to much higher alkali resistance compared to the commercial reference. Furthermore, two catalysts, i.e. 20 wt% V{sub 2}O-3-TiO{sub 2} nano-catalyst and the 4 wt% CuO-Mordenite zeolite based catalyst have also a higher initial SCR activity compared to the commercial one before alkali poisoning. Thus, those two catalysts might be attractive for SCR deNO{sub x} purposes even under ''normal'' fuel conditions in power plants and elsewhere making them strong candidates for further development. These efforts regarding all the promising catalysts will be pursued after this project has expired through a one year Proof of Concept project granted by the Danish Agency for Science, Technology and Innovation. Also the severe rate of deactivation due to alkali poisons can be avoided by coating the vanadium catalyst with Mg. Overall, the protective coating of SCR catalysts developed in the project seems promising and a patent application has been filed for this technology. Finally, a completely different approach to

  16. Electrical conduction and glass relaxation in alkali- silicate glasses (United States)

    Angel, Paul William

    Electrical response measurements from 1 Hz to 1 MHz between 50o and 540oC were made on potassium, sodium and lithium-silicate glasses with low alkali oxide contents. Conductivity and electrical relaxation responses for both annealed and air quenched glasses of the same composition were compared. Quenching was found to lower the dc conductivity, σdc, and activation energy as well as increase the pre-exponential term when compared to the corresponding annealed glass of the same composition. All of the glasses exhibited Arrhenius behavior in the log σdc against 1/T plots. A sharp decrease in σdc was observed for glasses containing alkali concentrations of 7 mol% or less. The σdc activation energy exhibited similar behavior when plotted as a function of alkali composition and was explained in terms of a mixture of the weak and strong electrolyte models. The depression angle for fits to the complex impedance data were also measured as a function of thermal history, alkali concentration and alkali species. These results were interpreted in terms of changes in the distribution of relaxation times. Annealed samples from a single melt of a 10 mol% K2O-90SiO2 glass were reheated to temperatures ranging from 450o to 800oC, held isothermally for 20 min, and then quenched in either air or silicon oil. The complex impedance of both an annealed and the quenched samples were then measured as a function of temperature from 120o to 250oC. The σdc was found to be remain unaffected by heat treatments below 450oC, to increase rapidly over an approximate 200oC range of temperatures that was dependent on cooling rate and to be constant for heat treatments above this range. This behavior is interpreted in terms of the mean structural relaxation time as a function of temperature and cooling rate near the glass transition temperature and glass transformation ranges. A more detailed definition for the transition and transformation temperatures and ranges was also provided.

  17. Path integral Monte Carlo study of 4He clusters doped with alkali and alkali-earth ions. (United States)

    Galli, D E; Ceperley, D M; Reatto, L


    Path integral Monte Carlo calculations of (4)He nanodroplets doped with alkali (Na(+), K(+) and Cs(+)) and alkali-earth (Be(+) and Mg(+)) ions are presented. We study the system at T = 1 K and between 14 and 128 (4)He atoms. For all studied systems, we find that the ion is well localized at the center of the droplet with the formation of a "snowball" of well-defined shells of localized (4)He atoms forming solid-like order in at least the first surrounding shell. The number of surrounding helium shells (two or three) and the number of atoms per shell and the degree of localization of the helium atoms are sensitive to the type of ion. The number of (4)He atoms in the first shell varies from 12 for Na(+) to 18 for Mg(+) and depends weakly on the size of the droplet. The study of the density profile and of the angular correlations shows that the local solid-like order is more pronounced for the alkali ions with Na(+) giving a very stable icosahedral order extending up to three shells.

  18. Structural analysis of alkali cations in mixed alkali silicate glasses by 23Na and 133Cs MAS NMR

    Directory of Open Access Journals (Sweden)

    T. Minami


    Full Text Available We report the structural analysis of Na+ and Cs+ in sodium cesium silicate glasses by using 23Na and 133Cs magic-angle spinning nuclear magnetic resonance (MAS NMR spectroscopy. In the NMR spectra of cesium silicate crystals, the peak position shifted to higher magnetic field for structures with larger Cs+ coordination numbers and to lower magnetic field for smaller Cs+ coordination numbers. The MAS NMR spectra of xNa2O-yCs2O-2SiO2 (x = 0, 0.2, 0.33, 0.5, 0.66, 0.8, 1.0; x + y = 1 glass reveal that the average coordination number of both the alkali cations decreases with increasing Cs+/(Na+ + Cs+ ratio. In addition, the coordination number of Na+ in xNa2O-yCs2O-2SiO2 glass is smaller than that of Cs+. This difference between the average coordination numbers of the alkali cations is considered to be one structural reason of the mixed alkali effect.

  19. Modifier interaction and mixed-alkali effect in bond constraint theory applied to ternary alkali metaphosphate glasses

    Directory of Open Access Journals (Sweden)

    Bruno ePoletto Rodrigues


    Full Text Available Introducing an interaction parameter γ, we implement modifier interaction and the mixed-alkali effect into bond constraint theory, and apply this extension for simplistic property prediction on ternary phosphate glasses. The severity of the mixed alkali effect results from the interplay of two simultaneous contributions: Bond constraints on the modifier species soften or stiffen with decreasing or increasing γ, respectively. When the modifier size is not too dissimilar the decrease in γ reflects that the alkali ions can easily migrate between different sites, forcing the network to continuously re-accommodate for any subsequent distortions. With increasing size difference, migration becomes increasingly difficult without considerable network deformation. This holds even for smaller ions, where the sluggish dynamics of the larger constituent result in blocking of the fast ion movement, leading to the subsequent increase in γ. Beyond a certain size difference in the modifier pair, a value of γ exceeding unity may indicate the presence of steric hindrance due to the large surrounding modifiers impeding the phosphate network to re-accommodate deformation.

  20. Pretreatment of garden biomass by alkali-assisted ultrasonication: effects on enzymatic hydrolysis and ultrastructural changes. (United States)

    Gabhane, Jagdish; William, Spm Prince; Vaidya, Atul Narayan; Anand, Duraisamy; Wate, Satish


    The present investigation aims at studying the effectiveness of alkali-assisted ultrasonication on pretreatment of garden biomass (GB). Dry and powdered GB suspended in 1% NaOH was ultrasonicated for 15, 30 and 60 minutes at a frequency of 25 KHZ. The mode of action and effectiveness of alkali-assisted ultrasonication on GB was established through microscopic, scanning electron microscopic and X-ray diffraction studies. A perusal of results showed that alkali-assisted ultrasonication led to fibrillation of GB which ultimately facilitated enzymatic hydrolysis. The results also indicated that alkali-assisted ultrasonication is an efficient means of pretreatment of GB at moderate (45-50°C) working temperature and low (1%) concentration of alkali. The yield of reducing sugar after enzymatic hydrolysis increased almost six times as compared to control due to alkali-assisted ultrasonication.

  1. Synthesis and characterization of laurate-intercalated Mg–Al layered double hydroxide prepared by coprecipitation

    DEFF Research Database (Denmark)

    Gerds, Nathalie Christiane; Katiyar, Vimal; Koch, Christian Bender


    Effective utilization of layered double hydroxides (LDH) for industrial applications requires the synthesis of pure and well-defined LDH phases. In the present study, dodecanoate (laurate) anions were intercalated into Mg–Al-layered double hydroxide (LDH-C12) by coprecipitation in the presence of...

  2. Mg/Al Ordering in Layered Double Hydroxides Revealed by Multinuclear NMR Spectroscopy

    DEFF Research Database (Denmark)

    Nielsen, Ulla Gro; Grey, Clare P.; Sideris, Paul J.


    The anion- exchange ability of layered double hydroxides ( LDHs) has been exploited to create materials for use in catalysis, drug delivery, and environmental remediation. The specific cation arrangements in the hydroxide layers of hydrotalcite- like LDHs, of general formula Mg1-x2+Alx3+OH2(Anion...

  3. Assessment of ion diffusion from a calcium hydroxide-propolis paste through dentin

    Directory of Open Access Journals (Sweden)

    Janaina Corazza Montero


    Full Text Available This study evaluated the ability of ions from a non-alcoholic calcium hydroxide-propolis paste to diffuse through dentinal tubules. Thirty-six single-rooted bovine teeth were used. The tooth crowns were removed, and the root canals were instrumented and divided into 3 groups: Group 1 - calcium hydroxide-propylene glycol paste; Group 2 - calcium hydroxide-saline solution paste; Group 3 - calcium hydroxide-propolis paste. After the root canal dressings were applied, the teeth were sealed and placed in containers with deionized water. The pH of the water was measured after 3, 24, 72 and 168 hours to determine the diffusion of calcium hydroxide ions through the dentinal tubules. All of the pastes studied promoted the diffusion of calcium hydroxide ions through the dentinal tubules. Associating propolis to calcium hydroxide resulted in a pH increase, which occurred with greater intensity after 72 hours. The calcium hydroxide-propolis paste was able to diffuse in dentin.

  4. Layered double hydroxide stability. 2. Formation of Cr(III)-containing layered double hydroxides directly from solution (United States)

    Boclair, J. W.; Braterman, P. S.; Jiang, J.; Lou, S.; Yarberry, F.


    Solutions containing divalent metal [M(II) = Mg2+, Zn2+, Co2+, Ni2+, Mn2+] chlorides and CrCl3 6H2O were titrated with NaOH to yield, for M(II) = Zn, Co, and Ni, hydrotalcite-like layered double hydroxides (LDHs), [[M(II)]1-z[Cr(III)]z(OH)2][Cl]z yH2O, in a single step, without intermediate formation of chromium hydroxide. Analysis of the resultant titration curves yields solubility constants for these compounds. These are in the order Zn < Ni approximately Co, with a clear preference for formation of the phase with z = 1/3. With Mg2+ as chloride, titration gives a mixture of Cr(OH)3 and Mg(OH)2, but the metal sulfates give Mg2Cr(OH)6 1/2(SO4) by a two-step process. Titrimetric and spectroscopic evidence suggests short-range cation order in the one-step LDH systems.

  5. Effect of Alkali Stress on Soluble Sugar, Antioxidant Enzymes and Yield of Oat

    Institute of Scientific and Technical Information of China (English)

    BAI Jian-hui; LIU Jing-hui; ZHANG Na; YANG Jun-heng; SA Ru-la; WU Lan


    Alkali stress can cause severe crop damage and reduce production. However, physiological processes involved in alkali stress in oat seedlings are not well understood. In this study, physiological responses and yield of oat to alkali stress were studied using the alkali-tolerant oat genotype Vao-9 and the alkali-sensitive oat genotype Baiyan 5. The results were:(i) low concentrations of alkali stress (25 and 50 mmol L-1) significantly reduced the yield and grain weight while increased the oat grain number per spike. A negative correlation between yield and malondialdehyde (MDA) content at the jointing and grain filling stages and positive correlations between yield on one hand and superoxide dismutase (SOD), and peroxidase (POD) activities on the other at the jointing stage were observed. There was a positive correlation between MDA and soluble sugar at the grain filling stage;(ii) soluble sugar content was increased at the jointing and grain filling stages and decreased at the heading stage by alkali stress;(iii) alkali stress increased the SOD activity during the heading and grain filling stages, and increased the POD activity at the heading stage. As compared to the control, the increase of MDA contents in alkali-treated oat was observed, during the jointing, heading and grain filling stages;(iv) under alkali stress, the oat genotype Vao-9 showed higher antioxidant enzyme activity and lower soluble sugar contents during the heading stage, and lower MDA contents than those in the oat genotype Baiyan 5 under alkali stress. The result suggested that the high ROS scavenging capacity and soluble sugar levels might play roles in oat response to alkali stress.

  6. Calculation of Radiative Corrections to E1 matrix elements in the Neutral Alkalis

    Energy Technology Data Exchange (ETDEWEB)

    Sapirstein, J; Cheng, K T


    Radiative corrections to E1 matrix elements for ns-np transitions in the alkali metal atoms lithium through francium are evaluated. They are found to be small for the lighter alkalis but significantly larger for the heavier alkalis, and in the case of cesium much larger than the experimental accuracy. The relation of the matrix element calculation to a recent decay rate calculation for hydrogenic ions is discussed, and application of the method to parity nonconservation in cesium is described.

  7. Decay curve analysis of alkali-silicate glass exposed to electrons

    CERN Document Server

    Gedeon, O


    Binary and ternary potassium, rubidium and caesium glasses were irradiated by an electron beam with energy varying from 10 to 50 keV. Alkali ion x-ray decays were recorded and afterward incubation periods were determined. The incubation period versus electron energy curves revealed thresholds, which are typical for each alkali species. The threshold ratios are proportional to the mass of the alkali species, consistent with the suggested elastic scattering assisted hopping mechanism. (author)

  8. Comparison of calcium hydroxide and zinc oxide and eugenol pulpectomies in primary teeth of dogs. (United States)

    Hendry, J A; Jeansonne, B G; Dummett, C O; Burrell, W


    The purpose of this investigation was to compare calcium hydroxide with zinc oxide and eugenol (ZOE) as root canal obturants in the pulpectomy procedure for irreversibly inflamed primary pulps of dogs. Clinical, radiographic, and histologic comparisons of calcium hydroxide and ZOE root canal filling materials were made in forty-two primary premolars of seven mongrel puppies. When the animals were 6 weeks of age, the pulps of all samples teeth were extirpated and the canals left open to the oral environment. The root canals were assigned to calcium hydroxide, ZOE, and control groups, instrumented, and filled 2 weeks later. The animals were killed 1 day, 1 week, 4 weeks, and 12 weeks after filling. Statistical analysis of all categories for comparison at 4 weeks indicated that calcium hydroxide gave significantly more favorable results than ZOE. Canals treated with calcium hydroxide exhibited less inflammation, less resorption, and more hard-tissue apposition than ZOE-treated and control groups.

  9. The Deactivation of Nickel Hydroxide to Hypophosphite Electrooxidation on a Nickel Electrode

    Institute of Scientific and Technical Information of China (English)

    Yue ZENG; Min MO; Jian Long YI; Xin Jun TANG; Hui Xian WANG


    The deactivation of nickel hydroxide to the electrooxidation of hypophosphite on a nickel electrode was studied by means of in situ UV-Vis subtractive reflectance spectroscopy. The experimental results show that when the potential is lower than -1.0 V (SCE), the surface on nickel electrode is free of nickel hydroxide, on which hypophosphite is active. When the potential moves positively to about-0.75V, two absorbency bands around 300 nm and 550 nm, which were ascribed to the formation of α-nickel hydroxide, were observed, nickel is oxidized to α-nickel hydroxide.Severe deactivation of the surface occurs when the nickel surface is covered with nickel hydroxide,which separates the hypophosphite ion from nickel substrate.

  10. Synthesis and structure refinement of layered double hydroxides of Co, Mg and Ni with Ga

    Indian Academy of Sciences (India)

    G V Manohara; P Vishnu Kamath


    Homogeneous precipitation by urea hydrolysis results in the formation of highly ordered layered double hydroxides of divalent metal ions (Co, Mg, Ni) and Ga. Structure refinement shows that these carbonate containing layered hydroxides crystallize with rhombohedral symmetry (space group -3) in the structure of the 31 polytype. An analysis of the structure shows that, coulombic attraction between the layer and interlayer remains invariant in different layered hydroxides, whereas the strength of hydrogen bonding varies. The Ni–Ga LDH has the weakest hydrogen bonding and Co–Ga, the strongest, as reflected by the layer–interlayer oxygen–oxygen distances. The poor polarity of the OH bond in the Ni–Ga hydroxide points to the greater covalency of the (2+}/′3+)-oxygen bond in this compound as opposed to the Co–Ga hydroxide. These observations are supported by IR spectra.

  11. Alkali-Silica Reaction Inhibited by LiOH and Its Mechanism

    Institute of Scientific and Technical Information of China (English)


    A high alkali reactive aggregate-zeolitization perlite was used to test the long-term effectiveness of LiOH in inhibiting alkali-silica reaction.In this paper,the rigorous conditions were designed that the mortar bars had been cured at 80℃ for 3 years after autoclaved 24 hours at 150℃.Under this condition,LiOH was able to inhibit the alkali-silica reaction long-term effectiveness.Not only the relationship between the molar ratio of n(Li)/(Na) and the alkali contents in systems was established, but also the governing mechanism of such effects was also studied by SEM.

  12. An optical sensor based on H-acid/layered double hydroxide composite film for the selective detection of mercury ion. (United States)

    Sun, Zhiyong; Jin, Lan; Zhang, Shitong; Shi, Wenying; Pu, Min; Wei, Min; Evans, David G; Duan, Xue


    A novel optical chemosensor was fabricated based on 1-amino-8-naphthol-3,6-disulfonic acid sodium (H-acid) intercalated layered double hydroxide (LDH) film via the electrophoretic deposition (EPD) method. The film of H-acid/LDH with the thickness of 1 μm possesses a well c-orientation of the LDH microcrystals confirmed by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The fluorescence detection for Hg(II) in aqueous solution was performed by using the H-acid/LDH film sensor at pH 7.0, with a linear response range in 1.0 × 10(-7) to 1.0 × 10(-5) mol L(-1) and a detection limit of 6.3 × 10(-8) mol L(-1). Furthermore, it exhibits excellent selectivity for Hg(II) over a large number of competitive cations including alkali, alkaline earth, heavy metal and transitional metals. The specific fluorescence response of the optical sensor is attributed to the coordination between Hg(II) and sulfonic group in the H-acid immobilized in the LDH matrix, which was verified by NMR spectroscopy and UV-vis spectra. In addition, density functional theory (DFT) calculation further confirms that the coordination occurs between one Hg(2+) and two O atoms in the sulfonic group, which is responsible for the significant fluorescence quenching of the H-acid/LDH film. The results indicate that the H-acid/LDH composite film can be potentially used as a chemosensor for the detection of Hg(2+) in the environmental and biomedical field.

  13. Hexamethylenetetramine directed synthesis and properties of a new family of alpha-nickel hydroxide organic-inorganic hybrid materials with high chemical stability. (United States)

    Liu, Bian-Hua; Yu, Shu-Hong; Chen, Shao-Feng; Wu, Chun-Yan


    A new family of organic-inorganic hybrid material of alpha-nickel hydroxide formulated as Ni(OH)2-x(An-)x/n-(C6H12N4)y.zH2O (A=Cl-, CH3COO-, SO4(2-), NO3-; x=0.05-0.18, y=0.09-0.11, z=0.36-0.43) with high stability and adjustable interlayer spacing ranging from 7.21 to 15.12 A has been successfully prepared by a simple hydrothermal method. The effects of various anions and hexamethylenetetramine (HMT) on the d values of alpha-nickel hydroxide have been systematically investigated. This family of hybrid materials is of such high stability that they can stand more than 40 days in 6 M KOH. The product with a formula Ni(OH)1.95(C6H12N4)0.11(Cl-)0.05(H2O)0.36 has a high surface area of about 299.26 m2/g and an average pore diameter of about 45.1 A. The coercivity (Hc) value is ca. 2000 Oe for the sample with a d spacing of 13.14 A. Moreover, the prepared alpha-Ni(OH)2 in our experiment is of high stability in strong alkali solution. Such high stability could be derived from strong chelating interactions between the Ni ions and HMT molecules with the interlayers. This high chemical stability could make this material more suitable for the applications.

  14. The Performance of Geopolymers Activated by Sodium Hydroxide. (United States)

    Hong, Hyeontaek; Kang, Seunggu


    Geopolymers, a group of promising environmentally friendly materials that can work as cement substitutes, should be fabricated from SiO2-Al2O3-CaO mixtures containing large amounts of amorphous phases to ensure optimal chemical and physical properties. In this study, it was shown that geopolymers with enhanced mechanical strengths, as high as 115 MPa, could be obtained from perfectly amorphous slag from spent catalyst (SSC) discharged during automobile catalyst recycling. Geopolymer processing involved alkali-activation using a 16 M NaOH solution of pH13. The varying SSC grain size was the main experimental factor of interest, in combination with curing temperature and aging time. Variations in the mechanical strengths of the resulting geopolymers are explained by the occurrence of 10-50 nm-sized crystals and the presence of voids and pores dozens to hundreds of micrometers in size.

  15. Application of Hydrosoluble Polymers to Preparation of Nanoscale Calcium Hydroxide

    Institute of Scientific and Technical Information of China (English)

    XU Jing; CHEN Qing-hua; QIAN Qing-rong


    Calcium hydroxide with uniform diameters about 50-100 nm was firstly prepared under moderate condition by adding different kinds of hydrosoluble polymers. From the results of TEM and IR, the polymers were proved not only to improve the agglomeration of the nanoparticles but also to be used as a template to control the formation of the special structure and the needed size of Ca (OH)2 by changing the concentration of the polymers. The experimental results of TG-DTA indicate that the Ca(OH)2 can absorb most of the acid gases released during the decomposition of polymers. So this kind of nano-Ca(OH)2 can be used as a useful additive of environmental friendly plastics.

  16. Layered Double Hydroxide-Based Nanocarriers for Drug Delivery

    Directory of Open Access Journals (Sweden)

    Xue Bi


    Full Text Available Biocompatible clay materials have attracted particular attention as the efficient drug delivery systems (DDS. In this article, we review developments in the use of layered double hydroxides (LDHs for controlled drug release and delivery. We show how advances in the ability to synthesize intercalated structures have a significant influence on the development of new applications of these materials. We also show how modification and/or functionalization can lead to new biotechnological and biomedical applications. This review highlights the most recent progresses in research on LDH-based controlled drug delivery systems, focusing mainly on: (i DDS with cardiovascular drugs as guests; (ii DDS with anti-inflammatory drugs as guests; and (iii DDS with anti-cancer drugs as guests. Finally, future prospects for LDH-based drug carriers are also discussed.

  17. Synthesis of tetramethyl ammonium hydroxide by cell diaphragm electrolytic method

    Institute of Scientific and Technical Information of China (English)


    Under the conditions of tetramethyl ammonia chloride (TMAC) used as starting material, Ti-based Dimensionally Stable Anode (DSA), stainless steel used as cathode and Nafion 900 cation membrane as cell diaphragm, this paper studies the synthesis of tetramethyl ammonium hydroxide (TMAH) by cell diaphragm electrolytic method, examining not only the effects of current density, concentration of starting material and cell temperature, on the product purity and current efficiency, but also the effects of electrolyte circulation rate on the service life of Ti-based DSA.The experiment puts forward an optimum processing condition, and experimental findings show that preparing TMAH by using this technique can obtain a current efficiency 74.7 % and get product with a purity greater than 99.9%.

  18. Hydrothermal Synthesis of Ni/Al Layered Double Hydroxide Nanorods

    Directory of Open Access Journals (Sweden)

    Yun Zhao


    Full Text Available Ni/Al layered double hydroxide (LDH nanorods were successfully synthesized by the hydrothermal reaction. The crystal structure of the products was characterized by X-ray diffraction (XRD. The morphology of the products was observed using transmission electron microscopy (TEM and field emission scanning electron microscopy (SEM. The influences of reaction time and pH value on the morphology of the Ni/Al LDHs were investigated. The result showed that the well-crystallized nanorods of Ni/Al LDHs could be obtained when the pH value was about 10.0 with a long reaction time (12–18 h at 180°C.

  19. Hydroxide as general base in the saponification of ethyl acetate. (United States)

    Mata-Segreda, Julio F


    The second-order rate constant for the saponification of ethyl acetate at 30.0 degrees C in H(2)O/D(2)O mixtures of deuterium atom fraction n (a proton inventory experiment) obeys the relation k(2)(n) = 0.122 s(-1) M(-1) (1 - n + 1.2n) (1 - n + 0.48n)/(1 - n + 1.4n) (1 - n + 0.68n)(3). This result is interpreted as a process where formation of the tetrahedral intermediate is the rate-determining step and the transition-state complex is formed via nucleophilic interaction of a water molecule with general-base assistance from hydroxide ion, opposite to the direct nucleophilic collision commonly accepted. This mechanistic picture agrees with previous heavy-atom kinetic isotope effect data of Marlier on the alkaline hydrolysis of methyl formate.

  20. Biological evaluation of layered double hydroxides as efficient drug vehicles

    Energy Technology Data Exchange (ETDEWEB)

    Li Yan; Liu Dan; Chang Qing; Liu Dandan; Xia Ying; Liu Shuwen; Peng Nanfang; Yang Xu [Hubei Key Laboratory of Genetic Regulation and Integrative Biology, College of Life Science, Huazhong Normal University, Wuhan 430079 (China); Ai Hanhua [College of Physical Science and Technology, Huazhong Normal University, Wuhan 430079 (China); Xi Zhuge, E-mail: [Tianjin Institutes of Health and Environmental Medicine, Tianjin 300050 (China)


    Recently there has been a rapid expansion of the development of bioinorganic hybrid systems for safe drug delivery. Layered double hydroxides (LDH), a variety of available inorganic matrix, possess great promise for this purpose. In this study, an oxidative stress biomarker system, including measurement of reactive oxygen species, glutathione content, endogenous nitric oxide, carbonyl content in proteins, DNA strand breaks and DNA-protein crosslinks, was designed to evaluate the biocompatibility of different concentrations of nano-Zn/Al-LDH with a Hela cell line. The drug delivery activity of the LDH-folic-acid complex was also assessed. The resulting data clearly demonstrated that nano-LDH could be applied as a relatively safe drug vehicle with good delivery activity, but with the caveat that the effects of high dosages observed here should not be ignored when attempting to maximize therapeutic activity by increasing LDH concentration.

  1. Electronic spectra of anions intercalated in layered double hydroxides

    Indian Academy of Sciences (India)

    S Radha; P Vishnu Kamath


    Transition metal complexes intercalated in layered double hydroxides have a different electronic structure as compared to their free state owing to their confinement within the interlayer gallery. UV–Vis absorptions of the intercalated complex anions show a significant shift as compared to their free state. The ligand to metal charge transfer transitions of the ferricyanide anion show a red shift on intercalation. The ferrocyanide ion shows a significant blue shift of – bands due to the increased separation between 2g and g levels on intercalation. MnO$^{-}_{4}$ ion shows a blue shift in its ligand to metal charge transfer transition since the non-bonding 1 level of oxygen from which the transition arises is stabilized.

  2. Polymerization reaction in restricted space of layered double hydroxides (LDHs)

    Institute of Scientific and Technical Information of China (English)

    SI Lichun; WANG Ge; CAI Fuli; WANG Zhiqiang; DUAN Xue


    This paper reported the preparation of styrene sulfonate intercalated layered double hydroxides (LDHs) material, SS-LDHs by coprecipitation method, followed by in-situ polymerization of the monomers in the interlayer space of LDHs. The polymerization reaction was monitored by UV and NMR. It is confirmed that when the reaction occurred at 100℃ for 24 h, part of monomers did not react .When the reaction was carried out at 150℃, the polymeriza tion of the intercalated monomers is complete to afford the polymer intercalated product PSS-LDHs. During the polymerization process, the layered structure remains well. At thesame time the gallery height increases with the lengthening of reaction time. This is preliminarily because that the PSS becomes more swelling with the amount of water it absorbs due to its hygroscopicity property.

  3. The kinetic parameters of carbonaceous materials activated with potassium hydroxide

    Energy Technology Data Exchange (ETDEWEB)

    Yong, Z.; Han, B.X.


    On the basis of microspore formation in carbonaceous materials, the activation energy for the potassium hydroxide activation of Chinese petroleum coke and coal has been deduced theoretically as dB(O)/dt = A exp(-E(a)) is an element of/RT), where is an element of is the formation energy for the metastable solid formed at the activation temperature. The kinetic parameters (frequency factor, A, and apparent activation energy, E(a) were calculated from this equation as being 5.319 mg/(g min), 36.51 kJ/mol and 6.64 mg/(g min), 49.46 kJ/mol, respectively, for the two carbonaceous materials studied.

  4. Structural characterisation of a layered double hydroxide nanosheet (United States)

    Funnell, Nicholas P.; Wang, Qiang; Connor, Leigh; Tucker, Matthew G.; O'Hare, Dermot; Goodwin, Andrew L.


    We report the atomic-scale structure of a Zn2Al-borate layered double hydroxide (LDH) nanosheet, as determined by reverse Monte Carlo (RMC) modelling of X-ray total scattering data. This study involves the extension of the RMC method to enable structural refinement of two-dimensional nanomaterials. The refined LDH models show the intra-layer geometry in this highly-exfoliated phase to be consistent with that observed in crystalline analogues, with the reciprocal-space scattering data suggesting a disordered arrangement of the Zn2+ and Al3+ cations within the nanosheet. The approach we develop is generalisable and so offers a method of characterising the structures of arbitrary nanosheet phases, including systems that support complex forms of disorder within the nanosheets themselves.We report the atomic-scale structure of a Zn2Al-borate layered double hydroxide (LDH) nanosheet, as determined by reverse Monte Carlo (RMC) modelling of X-ray total scattering data. This study involves the extension of the RMC method to enable structural refinement of two-dimensional nanomaterials. The refined LDH models show the intra-layer geometry in this highly-exfoliated phase to be consistent with that observed in crystalline analogues, with the reciprocal-space scattering data suggesting a disordered arrangement of the Zn2+ and Al3+ cations within the nanosheet. The approach we develop is generalisable and so offers a method of characterising the structures of arbitrary nanosheet phases, including systems that support complex forms of disorder within the nanosheets themselves. Electronic supplementary information (ESI) available. See DOI: 10.1039/c4nr01265h

  5. An Aluminum Magnesium Hydroxide Stearate-based Skin Barrier Protection Cream Used for the Management of Eczematous Dermatitis (United States)

    Bhambri, Sanjay; Michaels, Brent


    Eczematous dermatoses can often be very difficult to treat. An aluminum magnesium hydroxide stearate-based cream has recently become available for clinical use. Aluminum magnesium hydroxide stearate-based cream provides an alternative option in treating these dermatoses while providing barrier protection against external allergens and irritants. This article reviews various studies evaluating aluminum magnesium hydroxide stearate-based cream. PMID:21212843

  6. Interaction of alkali and alkaline earth ions with Ochratoxin A

    Energy Technology Data Exchange (ETDEWEB)

    Poor, Miklos [Institute of Laboratory Medicine, University of Pecs, Pecs H-7624 (Hungary); Kunsagi-Mate, Sandor; Matisz, Gergely; Li, Yin; Czibulya, Zsuzsanna [Department of General and Physical Chemistry, University of Pecs, Pecs H-7624 (Hungary); Janos Szentagothai Research Center, Pecs H-7624 (Hungary); Peles-Lemli, Beata [Department of General and Physical Chemistry, University of Pecs, Pecs H-7624 (Hungary); Koszegi, Tamas, E-mail: [Institute of Laboratory Medicine, University of Pecs, Pecs H-7624 (Hungary)


    The effect of alkali and alkaline earth ions on the chemical equilibrium of mono- and dianionic forms of the mycotoxin Ochratoxin A (OTA) and their bonding onto the surface of Bovine Serum Albumin (BSA) have been investigated by fluorescence spectroscopy and fluorescence polarization techniques. Our results show that alkali metal ions shift the chemical equilibrium towards formation of dianionic form of OTA. Furthermore, the alkaline earth ions can compete with BSA for binding to OTA when these ions are present in millimolar concentrations. Our data also highlight the possibility that the 'free' fraction of OTA (not bound onto the surface of albumin) or at least a part of it is present in cation-bound form in body fluids. These observations are supported by stability constants and quantum-chemical calculations. Among the studied alkaline metal ions magnesium showed the highest affinity towards OTA under physiological conditions. Further research is required to analyze the potential significance of Mg{sup 2+}-OTA complex in cellular uptake and/or elimination of the toxin in the human body. - Highlights: Black-Right-Pointing-Pointer Fluorescence spectroscopy reveals cation-Ochratoxin A (OTA) interactions. Black-Right-Pointing-Pointer Alkali ions shift the equilibrium of OTA to formation of a dianionic structure. Black-Right-Pointing-Pointer Alkaline earth ions directly bind to OTA in the order: Mg{sup 2+}, Ca{sup 2+}, Ba{sup 2+}. Black-Right-Pointing-Pointer Quantum chemical calculations and logK values support our experimental data.

  7. Exotic s-wave superconductivity in alkali-doped fullerides. (United States)

    Nomura, Yusuke; Sakai, Shiro; Capone, Massimo; Arita, Ryotaro


    Alkali-doped fullerides (A3C60 with A = K, Rb, Cs) show a surprising phase diagram, in which a high transition-temperature (Tc) s-wave superconducting state emerges next to a Mott insulating phase as a function of the lattice spacing. This is in contrast with the common belief that Mott physics and phonon-driven s-wave superconductivity are incompatible, raising a fundamental question on the mechanism of the high-Tc superconductivity. This article reviews recent ab initio calculations, which have succeeded in reproducing comprehensively the experimental phase diagram with high accuracy and elucidated an unusual cooperation between the electron-phonon coupling and the electron-electron interactions leading to Mott localization to realize an unconventional s-wave superconductivity in the alkali-doped fullerides. A driving force behind the exotic physics is unusual intramolecular interactions, characterized by the coexistence of a strongly repulsive Coulomb interaction and a small effectively negative exchange interaction. This is realized by a subtle energy balance between the coupling with the Jahn-Teller phonons and Hund's coupling within the C60 molecule. The unusual form of the interaction leads to a formation of pairs of up- and down-spin electrons on the molecules, which enables the s-wave pairing. The emergent superconductivity crucially relies on the presence of the Jahn-Teller phonons, but surprisingly benefits from the strong correlations because the correlations suppress the kinetic energy of the electrons and help the formation of the electron pairs, in agreement with previous model calculations. This confirms that the alkali-doped fullerides are a new type of unconventional superconductors, where the unusual synergy between the phonons and Coulomb interactions drives the high-Tc superconductivity.

  8. Exotic s-wave superconductivity in alkali-doped fullerides (United States)

    Nomura, Yusuke; Sakai, Shiro; Capone, Massimo; Arita, Ryotaro


    Alkali-doped fullerides ({{A}3}{{\\text{C}}60} with A  =  K, Rb, Cs) show a surprising phase diagram, in which a high transition-temperature ({{T}\\text{c}} ) s-wave superconducting state emerges next to a Mott insulating phase as a function of the lattice spacing. This is in contrast with the common belief that Mott physics and phonon-driven s-wave superconductivity are incompatible, raising a fundamental question on the mechanism of the high-{{T}\\text{c}} superconductivity. This article reviews recent ab initio calculations, which have succeeded in reproducing comprehensively the experimental phase diagram with high accuracy and elucidated an unusual cooperation between the electron-phonon coupling and the electron-electron interactions leading to Mott localization to realize an unconventional s-wave superconductivity in the alkali-doped fullerides. A driving force behind the exotic physics is unusual intramolecular interactions, characterized by the coexistence of a strongly repulsive Coulomb interaction and a small effectively negative exchange interaction. This is realized by a subtle energy balance between the coupling with the Jahn-Teller phonons and Hund’s coupling within the {{\\text{C}}60} molecule. The unusual form of the interaction leads to a formation of pairs of up- and down-spin electrons on the molecules, which enables the s-wave pairing. The emergent superconductivity crucially relies on the presence of the Jahn-Teller phonons, but surprisingly benefits from the strong correlations because the correlations suppress the kinetic energy of the electrons and help the formation of the electron pairs, in agreement with previous model calculations. This confirms that the alkali-doped fullerides are a new type of unconventional superconductors, where the unusual synergy between the phonons and Coulomb interactions drives the high-{{T}\\text{c}} superconductivity.

  9. Reactivity of clay minerals with acids and alkalies (United States)

    Carroll, D.; Starkey, H.C.


    One-g samples of a montmorillonite, a metabentonite, an illite, two kaolinites, and three halloysites were treated with 50 ml of hydrochloric acid (6??45 N, 1:1), acetic acid (4??5 N, 1:3), sodium hydroxide (2??8 N), sodium chloride solution (pH 6??10; Na = 35???; Cl = 21??5???), and natural sea water (pH 7??85; Na = 35??5???; Cl = 21??5???) for a 10-day period in stoppered plastic vials. The supernatant solutions were removed from the clay minerals and analyzed for SiO2, Al2O3, CaO, MgO, Na2O, and K2O. All the solutions removed some SiO2, Al2O3, and Fe2O3 from the samples, but the quantities were small. Sodium hydroxide attacked the kaolin group minerals more strongly than it did montmorillonite, metabentonite, or illite. Halloysite was more strongly attacked by hydrochloric acid than was any of the other experimental minerals. Hydrochloric acid removed iron oxide coatings from soil clay minerals, but acetic acid did not remove them completely. The samples most strongly attacked by HCl and NaOH were examined by X-ray diffraction. Acid treatment did not destroy the structure of the clays, but the halloysite structure was partially destroyed. Sodium hydroxide attacked the halloysite structure, as shown by chemical analysis and X-ray diffraction. These experiments show that treatment in dilute acids has no harmful effect in the preparation of clays for X-ray diffraction. Acetic acid is preferred to hydrochloric acid for this purpose. Hydrochloric acid cleans clay minerals by removing free iron oxide from the surface; acetic acid is less effective. ?? 1971.

  10. Fabrication method for microscopic vapor cells for alkali atoms. (United States)

    Baluktsian, T; Urban, C; Bublat, T; Giessen, H; Löw, R; Pfau, T


    A quantum network that consists of several components should ideally work on a single physical platform. Neutral alkali atoms have the potential to be very well suited for this purpose due to their electronic structure, which involves long-lived nuclear spins and very sensitive highly excited Rydberg states. In this Letter, we describe a fabrication method based on quartz glass to structure arbitrary shapes of microscopic vapor cells. We show that the usual spectroscopic properties known from macroscopic vapor cells are almost unaffected by the strong confinement.

  11. Electric dipole polarizabilities of Rydberg states of alkali atoms

    CERN Document Server

    Yerokhin, V A; Fritzsche, S; Surzhykov, A


    Calculations of the static electric-dipole scalar and tensor polarizabilities are presented for two alkali atoms, Rb and Cs, for the $nS$, $nP_{1/2, 3/2}$, and $nD_{3/2, 5/2}$ states with large principal quantum numbers up to $n = 50$. The calculations are performed within an effective one-electron approximation, based on the Dirac-Fock Hamiltonian with a semi-empirical core-polarization potential. The obtained results are compared with those from a simpler semi-empirical approach and with available experimental data.

  12. Integrated oil production and upgrading using molten alkali metal

    Energy Technology Data Exchange (ETDEWEB)

    Gordon, John Howard


    A method that combines the oil retorting process (or other process needed to obtain/extract heavy oil or bitumen) with the process for upgrading these materials using sodium or other alkali metals. Specifically, the shale gas or other gases that are obtained from the retorting/extraction process may be introduced into the upgrading reactor and used to upgrade the oil feedstock. Also, the solid materials obtained from the reactor may be used as a fuel source, thereby providing the heat necessary for the retorting/extraction process. Other forms of integration are also disclosed.

  13. Magnesia Modification of Alkali-Activated Slag Fly Ash Cement

    Institute of Scientific and Technical Information of China (English)

    SHEN Weiguo; WANG Yiheng; ZHANG Tao; ZHOU Mingkai; LI Jiasheng; CUI Xiaoyu


    A new type of magnesia modification alkali-activated cement was prepared, the strength, setting time, shrinkage ratio and cracking behavior, as well as the composition and structure of the hydration product were investigated. The results indicate that the setting time of this cement is similar to that of the ordinary commercial cements; its strength reaches the standard of 42.5 degree cement, its cracking resistance has been remarkably improved because of the micro-aggregate effect of fly ash and shrinkage compensating of magnesia.

  14. Hypercalcemic encephalopathy due to milk alkali syndrome and injection teriparatide

    Directory of Open Access Journals (Sweden)

    Sandeep Kharb


    Full Text Available An 82-year-old male, a known case of severe osteoporosis with vertebral fracture and prostatic carcinoma, was treated with gonadotropin releasing hormone analogue, calcium carbonate, cholecalciferol sachet and injection teriparatide. His diet consisted of milk and curd. He developed altered behavior and generalized weakness, and on investigation, hypercalcemia, hypokalemia, and metabolic alkalosis with low parathyroid hormone levels were detected. Injection teriparatide was stopped and he was managed with forced saline diuresis and injection zoledronic acid. He was diagnosed as a case of milk alkali syndrome in whom teriparatide and prolonged immobilization played a permissive role in the development of hypercalcemic encephalopathy.

  15. Chemical compatibility of structural materials in alkali metals

    Energy Technology Data Exchange (ETDEWEB)

    Natesan, K.; Rink, D.L.; Haglund, R. [Argonne National Lab., Chicago, IL (United States)] [and others


    The objectives of this task are to (a) evaluate the chemical compatibility of structural alloys such as V-5 wt.%Cr-5 wt.%Ti alloy and Type 316 stainless steel for application in liquid alkali metals such as lithium and sodium-78 wt.% potassium (NaK) at temperatures in the range that are of interest for International Thermonuclear Experimental Reactor (ITER); (b) evaluate the transfer of nonmetallic elements such as oxygen, nitrogen, carbon, and hydrogen between structural materials and liquid metals; and (c) evaluate the effects of such transfers on the mechanical and microstructural characteristics of the materials for long-term service in liquid-metal-environments.

  16. Analysis and modeling of alkali halide aqueous solutions

    DEFF Research Database (Denmark)

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


    A new model is proposed for correlation and prediction of thermodynamic properties of electrolyte solutions. In the proposed model, terms of a second virial coefficient-type and of a KT-UNIFAC model are used to account for a contribution of binary interactions between ion and ion, and water and ion...... on calculations for various electrolyte properties of alkali halide aqueous solutions such as mean ionic activity coefficients, osmotic coefficients, and salt solubilities. The model covers highly nonideal electrolyte systems such as lithium chloride, lithium bromide and lithium iodide, that is, systems...

  17. Precision two-photon spectroscopy of alkali elements

    Indian Academy of Sciences (India)

    P V Kiran Kumar; M V Suryanarayana


    In this paper, we have briefly reviewed the work on two-photon spectroscopy of alkali elements and its applications. The technique of Doppler-free two-photon spectroscopy is briefly summarized. A review of various techniques adopted for measuring absolute frequencies of the atomic transitions and precision measurements of isotope shifts and hyperfine structures (HFS) is presented. Some of the recent works on precision measurements of HFS constants of 6 ${}^2S_{1/2}$ level of ${}^{39}$K and ${}^{41}$K, 9 ${}^2S_{1/2}$ level and 7 ${}^2D_{3/2}$ level of 133Cs are also discussed.

  18. Electrochemical synthesis of alkali-intercalated iron selenide superconductors

    Institute of Scientific and Technical Information of China (English)

    申士杰; 应天平; 王刚; 金士锋; 张韩; 林志萍; 陈小龙


    Electrochemical method has been used to insert K/Na into FeSe lattice to prepare alkali-intercalated iron selenides at room temperature. Magnetization measurement reveals that KxFe2Se2 and NaxFe2Se2 are superconductive at 31 K and 46 K, respectively. This is the first successful report of obtaining metal-intercalated FeSe-based high-temperature superconductors using electrochemical method. It provides an effective route to synthesize metal-intercalated layered compounds for new superconductor exploration.

  19. Surface phonons on Al(111) surface covered by alkali metals (United States)

    Rusina, G. G.; Eremeev, S. V.; Borisova, S. D.; Sklyadneva, I. Yu.; Chulkov, E. V.


    We investigated the vibrational and structural properties of the Al(111)-(3×3)R30°-AM (AM=Na,K,Li) adsorbed systems using interaction potentials from the embedded-atom method. The surface relaxation, surface phonon dispersion, and polarization of vibrational modes for the alkali adatoms and the substrate atoms as well as the local density of states are discussed. Our calculated structural parameters are in close agreement with experimental and ab initio results. The obtained vibrational frequencies compare fairly well with the available experimental data.

  20. Wave optics simulation of diode pumped alkali laser (DPAL) (United States)

    Endo, Masamori; Nagaoka, Ryuji; Nagaoka, Hiroki; Nagai, Toru; Wani, Fumio


    A numerical simulation code for a diode pumped alkali laser (DPAL) was developed. The code employs the Fresnel- Kirchhoff diffraction integral for both laser mode and pump light propagations. A three-dimensional rate equation set was developed to determine the local gain. The spectral divergence of the pump beam was represented by a series of monochromatic beams with different wavelengths. The calculated results showed an excellent agreements with relevant experimental results. It was found that the main channel of the pump power drain is the spontaneous emission from the upper level of the lasing transition.

  1. Theoretical determination of the alkali-metal superoxide bond energies (United States)

    Partridge, Harry; Bauschlicher, Charles W., Jr.; Sodupe, Mariona; Langhoff, Stephen R.


    The bond dissociation energies for the alkali-metal superoxides have been computed using extensive Gaussian basis sets and treating electron correlation at the modified coupled-pair functional level. Our computed D0 values are 61.4, 37.2, 40.6, and 38.4 kcal/mol for LiO2, NaO2, KO2, and RbO2, respectively. These values, which are expected to be lower bounds and accurate to 2 kcal/mol, agree well with some of the older flame data, but rule out several recent experimental measurements.

  2. Effects of Heavy Metals and Saline-alkali on Growth, Physiology and Biochemistry of Orychophragmus violaceus

    Institute of Scientific and Technical Information of China (English)

    Xiaoai ZHANG; Zhihui WANG; Xinquan ZHANG; Mingyang Ll; Jing ZUO


    Abstract [Oh.jective] The aim was to study on effects of heavy metals and saline-al- kali on growth, physiology and biochemistry of Orychophragmus violaceus. [Method] Taken Orychophragmus violaceus as materials, growth, physiology and biochemistry were explored under stress of saline-alkali and heavy metals (light, moderate and se- vere saline-alkali, Pb, Pb + Cd, light saline-alkali + Pb, moderate saline-alkali + Pb, severe saline-alkali + Pb, light saline-alkali + Pb + Cd, moderate saline-alkali + Pb + Cd and severe saline-alkali + Pb + Cd) with control group set. [Result] Light stress of saline-alkali had little effect on membrane permeability, as follows: MDA contents in leaves and root systems declined by 25.6% and 9.0% compared with control group; Pb (500 mg/L) stress promoted synthetization of photosynthetic pigments, as follows: chlorophyll a and b and carotenoid increased by 0.86%, 0.69% and 6.25% than those of control group; combined stresses of Pb and Cd destroyed synthetization of photosynthetic pigments, among which carotenoid was more sensitive; under com- bined stresses of saline-alkali, Pb and Cd, POD and SOD activities, soluble saccha- rides and Pro content all increased and activities of POD and SOD in root system were both higher than those in leaves. [Conclusion] Orychophragmus violaceus is with resistance against light combined stresses of saline-alkali and Pb (500 mg/L).

  3. Food composition and acid-base balance: alimentary alkali depletion and acid load in herbivores. (United States)

    Kiwull-Schöne, Heidrun; Kiwull, Peter; Manz, Friedrich; Kalhoff, Hermann


    Alkali-enriched diets are recommended for humans to diminish the net acid load of their usual diet. In contrast, herbivores have to deal with a high dietary alkali impact on acid-base balance. Here we explore the role of nutritional alkali in experimentally induced chronic metabolic acidosis. Data were collected from healthy male adult rabbits kept in metabolism cages to obtain 24-h urine and arterial blood samples. Randomized groups consumed rabbit diets ad libitum, providing sufficient energy but variable alkali load. One subgroup (n = 10) received high-alkali food and approximately 15 mEq/kg ammonium chloride (NH4Cl) with its drinking water for 5 d. Another group (n = 14) was fed low-alkali food for 5 d and given approximately 4 mEq/kg NH4Cl daily for the last 2 d. The wide range of alimentary acid-base load was significantly reflected by renal base excretion, but normal acid-base conditions were maintained in the arterial blood. In rabbits fed a high-alkali diet, the excreted alkaline urine (pH(u) > 8.0) typically contained a large amount of precipitated carbonate, whereas in rabbits fed a low-alkali diet, both pH(u) and precipitate decreased considerably. During high-alkali feeding, application of NH4Cl likewise decreased pH(u), but arterial pH was still maintained with no indication of metabolic acidosis. During low-alkali feeding, a comparably small amount of added NH4Cl further lowered pH(u) and was accompanied by a significant systemic metabolic acidosis. We conclude that exhausted renal base-saving function by dietary alkali depletion is a prerequisite for growing susceptibility to NH4Cl-induced chronic metabolic acidosis in the herbivore rabbit.

  4. Evaluation of antibacterial effects of different calcium hydroxide compositions on planktonic Enterococcus faecalis

    Directory of Open Access Journals (Sweden)

    Mahdi Tabrizizadeh


    Full Text Available Background and Aims: Calcium hydroxide has a pronounced antimicrobial activity against most of the bacterial species found in infected root canals and endodontic infections. It is one of the most frequently used intracanal medications in endodontic therapy. The objective of this study was to determine the antimicrobial efficacy of six calcium hydroxide formulations (mixed with saline, lidocaine 2%, chlorhexidine 2%, chlorhexidine 0.2%, Iodine Potassium iodide (IKI 2%, and glycerin on Enterococcus faecalis using agar diffusion test.Materials and Methods: Twelve culture plates were incubated with Enterococcus faecalis. Five cavities were made in each plate with 5 mm diameter and 4 mm depth. Two plates were randomly considered for each calcium hydroxide formulation and filled completely with creamy mixture of tested materials. The plates were incubated at 37ºC for 48 hours. The diameter of inhibition zone around each well was recorded in millimetres and data were submitted to ANOVA and Tukey tests.Results: The results of this study showed that all tested calcium hydroxide pastes had good antimicrobial activity. The antimicrobial activity of calcium hydroxide mixed with lidocaine, chlorhexidine 2% and IKI 2% were significantly greater than that of calcium hydroxide mixed with saline (P0.01.Conclusion: Considering the results of this study, lidocaine 2%, chlorhexidine 2% and IKI 2% are suggested to be used for preparation of calcium hydroxide paste. Further studies with different methods are needed for confirming these results.

  5. Dispersion coefficients for the interaction of inert gas atoms with alkali and alkaline earth ions and alkali atoms with their singly ionized ions

    CERN Document Server

    Singh, Sukhjit; Sahoo, B K; Arora, Bindiya


    We report the dispersion coefficients for the interacting inert gas atoms with the alkali ions, alkaline earth ions and alkali atoms with their singly charged ions. We use our relativistic coupled-cluster method to determine dynamic dipole and quadrupole polarizabilities of the alkali atoms and singly ionized alkaline earth atoms, whereas a relativistic random phase approximation approach has been adopted to evaluate these quantities for the closed-shell configured inert gas atoms and the singly and doubly ionized alkali and alkaline earth atoms, respectively. Accuracies of these results are adjudged from the comparison of their static polarizability values with their respective experimental results. These polarizabilities are further compared with the other theoretical results. Reason for the improvement in the accuracies of our estimated dispersion coefficients than the data listed in [At. Data and Nucl. Data Tables 101, 58 (2015)] are discussed. Results for some of the atom-ion interacting systems were not...

  6. Structural Investigation of Alkali Activated Clay Minerals for Application in Water Treatment Systems (United States)

    Bumanis, G.; Bajare, D.; Dembovska, L.


    Alkali activation technology can be applied for a wide range of alumo-silicates to produce innovative materials with various areas of application. Most researches focuse on the application of alumo-silicate materials in building industry as cement binder replacement to produce mortar and concrete [1]. However, alkali activation technology offers high potential also in biotechnologies [2]. In the processes where certain pH level, especially alkaline environment, must be ensured, alkali activated materials can be applied. One of such fields is water treatment systems where high level pH (up to pH 10.5) ensures efficient removal of water pollutants such as manganese [3]. Previous investigations had shown that alkali activation technology can be applied to calcined clay powder and aluminium scrap recycling waste as a foam forming agent to create porous alkali activated materials. This investigation focuses on the structural investigation of calcined kaolin and illite clay alkali activation processes. Chemical and mineralogical composition of both clays were determined and structural investigation of alkali activated materials was made by using XRD, DTA, FTIR analysis; the microstructure of hardened specimens was observed by SEM. Physical properties of the obtained material were determined. Investigation indicates the essential role of chemical composition of the clay used in the alkali activation process, and potential use of the obtained material in water treatment systems.

  7. Effect of the Composite of Natural Zeolite and Fly Ash on Alkali-Silica Reaction

    Institute of Scientific and Technical Information of China (English)

    FENG Xiao-xin; FENG Nai-qian; HAN Dong


    The effect of the composite of natural zeolite and fly ash on alkali-silica reaction ( ASR ) was studied with natural alkali-reactive aggregate and quartz glass aggregate respecthvely. The expansive experiment of mortar bar and concrete prism was completed. The results show that ASR can be suppressed effectively by the composite of natural zeolite and fly ash.

  8. Hydration number of alkali metal ions determined by insertion in a conducting polymer

    DEFF Research Database (Denmark)

    Skaarup, Steen


    . The solvation of alkali metal ions has been discussed for many years without a clear consensus. This work presents a systematic study of the hydration numbers of the 5 alkali metal ions, using the electrochemical insertion of the ions in a conducting polymer (polypyrrole containing the large immobile anion DBS...

  9. The Effects of Biochar on Germination and Growth of Wheat in Different Saline-alkali Soil

    Institute of Scientific and Technical Information of China (English)

    Guijun; WANG; Zhenwen; XU


    Saline alkali soil can cause physiological drought on crops,so only some salinity tolerant crops can grow in saline alkali soil.Biochar can increase the utilize efficiency of nutrient and the water retention of the soil,and affect the growth of the plant.In this research,four different proportion of biochar was added in five different levels of saline-alkali soil for pot culture experiment.The pH of the soil increases as the proportion of biochar increase in same saline-alkali level soil,while the EC decrease as the proportion of biochar increase.The germination rate of wheat seeds varies as the different of soil’s saline-alkali level.Notable among these results is the germination of wheat seeds in the serious saline-alkali soil without biochar added is 0,while in 45%biochar added in serious saline-alkali soil,the germination rate get to as high as 48.9%.Also,biochar improve the growth of wheat seedling,while for mild saline alkali soil and normal soil.Biochar had no obvious effect on the growth of wheat seedling.

  10. In situ alkali-silica reaction observed by x-ray microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Kurtis, K.E.; Monteiro, P.J.M. [Univ. of California, Berkeley, CA (United States); Brown, J.T.; Meyer-Ilse, W. [Ernest Orlando Lawrence Berkeley National Lab., CA (United States)


    In concrete, alkali metal ions and hydroxyl ions contributed by the cement and reactive silicates present in aggregate can participate in a destructive alkali-silica reaction (ASR). This reaction of the alkalis with the silicates produces a gel that tends to imbibe water found in the concrete pores, leading to swelling of the gel and eventual cracking of the affected concrete member. Over 104 cases of alkali-aggregate reaction in dams and spillways have been reported around the world. At present, no method exists to arrest the expansive chemical reaction which generates significant distress in the affected structures. Most existing techniques available for the examination of concrete microstructure, including ASR products, demand that samples be dried and exposed to high pressure during the observation period. These sample preparation requirements present a major disadvantage for the study of alkali-silica reaction. Given the nature of the reaction and the affect of water on its products, it is likely that the removal of water will affect the morphology, creating artifacts in the sample. The purpose of this research is to observe and characterize the alkali-silica reaction, including each of the specific reactions identified previously, in situ without introducing sample artifacts. For observation of unconditioned samples, x-ray microscopy offers an opportunity for such an examination of the alkali-silica reaction. Currently, this investigation is focusing on the effect of calcium ions on the alkali-silica reaction.

  11. Alkali chloride induced corrosion of superheaters under biomass firing conditions: Improved insights from laboratory scale studies

    DEFF Research Database (Denmark)

    Okoro, Sunday Chukwudi; Montgomery, Melanie; Jappe Frandsen, Flemming


    to the formation of corrosive deposits (rich in alkali chlorides) on the surfaces of the superheaters. Accordingly, an extensive number of fundamental investigations have been undertaken to understand the basic mechanisms behind the alkali chloride induced high temperature corrosion of superheaters (for example...

  12. Desorption of alkali atoms from 4He nanodroplets. (United States)

    Hernando, Alberto; Barranco, Manuel; Pi, Martí; Loginov, Evgeniy; Langlet, Marina; Drabbels, Marcel


    The dynamics following the photoexcitation of Na and Li atoms located on the surface of helium nanodroplets has been investigated in a joint experimental and theoretical study. Photoelectron spectroscopy has revealed that excitation of the alkali atoms via the (n + 1)s ←ns transition leads to the desorption of these atoms. The mean kinetic energy of the desorbed atoms, as determined by ion imaging, shows a linear dependence on excitation frequency. These experimental findings are analyzed within a three-dimensional, time-dependent density functional approach for the helium droplet combined with a Bohmian dynamics description of the desorbing atom. This hybrid method reproduces well the key experimental observables. The dependence of the observables on the impurity mass is discussed by comparing the results obtained for the (6)Li and (7)Li isotopes. The calculations show that the desorption of the excited alkali atom is accompanied by the creation of highly non-linear density waves in the helium droplet that propagate at supersonic velocities.

  13. Structure and Bonding in Small Neutral Alkali-Halide Clusters

    CERN Document Server

    Aguado, A; López, J M; Alonso, J A


    The structural and bonding properties of small neutral alkali-halide clusters (AX)n, with n less than or equal to 10, A=Li, Na, K, Rb and X=F, Cl, Br, I, are studied using the ab initio Perturbed Ion (aiPI) model and a restricted structural relaxation criterion. A trend of competition between rock-salt and hexagonal ring-like isomers is found and discussed in terms of the relative ionic sizes. The main conclusion is that an approximate value of r_C/r_A=0.5 (where r_C and r_A are the cationic and anionic radii) separates the hexagonal from the rock-salt structures. The classical electrostatic part of the total energy at the equilibrium geometry is enough to explain these trends. The magic numbers in the size range studied are n= 4, 6 and 9, and these are universal since they occur for all alkali-halides and do not depend on the specific ground state geometry. Instead those numbers allow for the formation of compact clusters. Full geometrical relaxations are considered for (LiF)n (n=3-7) and (AX)_3 clusters, an...

  14. Thermal, mechanical and Raman studies on mixed alkali borotungstate glasses

    Energy Technology Data Exchange (ETDEWEB)

    Edukondalu, A. [Department of Physics, Osmania University, Hyderabad 500007 (India); Sathe, Vasant [Consortium for Scientific Research, Khandwa Road, Indore 452017 (India); Rahman, Syed [Department of Physics, Osmania University, Hyderabad 500007 (India); Siva Kumar, K., E-mail: [Department of Physics, Osmania University, Hyderabad 500007 (India)


    Mixed alkali borotungstate glasses with xLi{sub 2}O–(30−x)Na{sub 2}O–10WO{sub 3}–60B{sub 2}O{sub 3} (0 ≤ x ≤ 30) composition were prepared by melt quench technique. The amorphous phase of the prepared glass samples was conformed from their X-ray diffraction and SEM studies. Differential scanning calorimetry and Raman spectroscopic studies were employed to investigate the structure of all the prepared glasses. The elastic moduli and Debye temperature were calculated in terms of Makishima–Mackenzie model. Acting as complementary techniques, Raman measurement revealed that the network structure of the present glasses is mainly based on BO{sub 3} and BO{sub 4} units placed in different structural groups. Raman spectra confirms the presence of tungsten ions mainly as WO{sub 6} groups. In the present work, the mixed alkali effect (MAE) has been investigated in the above glass system through modulated DSC studies.

  15. Microstructural and Mechanical Properties of Alkali Activated Colombian Raw Materials

    Directory of Open Access Journals (Sweden)

    Maria Criado


    Full Text Available Microstructural and mechanical properties of alkali activated binders based on blends of Colombian granulated blast furnace slag (GBFS and fly ash (FA were investigated. The synthesis of alkali activated binders was conducted at 85 °C for 24 h with different slag/fly ash ratios (100:0, 80:20, 60:40, 40:60, 20:80, and 0:100. Mineralogical and microstructural characterization was carried out by means of X-ray diffraction (XRD, Fourier transform infrared spectroscopy (FTIR, Scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM/EDX and Nuclear magnetic resonance (NMR. Mechanical properties were evaluated through the compressive strength, modulus of elasticity and Poisson’s ratio. The results show that two different reaction products were detected in the slag/fly ash mixtures, a calcium silicate hydrate with Al in its structure (C-A-S-H gel and a sodium aluminosilicate hydrate (N-A-S-H gel with higher number of polymerized species and low content in Ca. It was found that with the increase of the amount of added slag, the amount of C-A-S-H gel increased and the amount of N-A-S-H gel decreased. The matrix was more dense and compact with almost absence of pores. The predominance of slag affected positively the compressive strength, Young’s modulus and Poisson’s ratio, with 80% slag and 20% fly ash concrete being the best mechanical performance blend.

  16. Periodic DFT approaches to crystalline alkali metal azides

    Institute of Scientific and Technical Information of China (English)


    The energy bands, electronic structures andrelationship between structures and properties of the crys-talline alkali metal azides, LiN3, α-NaN3 and KN3, are investigated at the DFT-B3LYP level. The crystalline bulks arepredicted to be insulator, speculated from their band gaps ofca. 0.23-0.25 a.u. and from their level frontier bands. Theatomic overlaps and electron densities show that the metalsand the azides are combined by ionic bonds. The crystal lat-tice energies, being corrected for the basis set superpositionerrors, are -852.30, -771.45 and - 614.78 kJ @ mol-1 for LiN3,α-NaN3 and KN3 respectively. These values are similar tothose by Gray's approximate method. The frontier crystalorbital mainly consists of the atomic orbital of the terminalnitrogen of azides. The contribution of the metallic orbital tothe LUMO is very small. The electron transition from theHOMO to the LUMO is difficult to occur. Hence all the al-kali metal azides are expected to be insensitive explosives,according to the "principle of easiest electron transition".

  17. High and rapid alkali cation storage in ultramicroporous carbonaceous materials (United States)

    Yun, Young Soo; Lee, Seulbee; Kim, Na Rae; Kang, Minjee; Leal, Cecilia; Park, Kyu-Young; Kang, Kisuk; Jin, Hyoung-Joon


    To achieve better supercapacitor performance, efforts have focused on increasing the specific surface area of electrode materials to obtain higher energy and power density. The control of pores in these materials is one of the most effective ways to increase the surface area. However, when the size of pores decreases to a sub-nanometer regime, it becomes difficult to apply the conventional parallel-plate capacitor model because the charge separation distance (d-value) of the electrical double layer has a similar length scale. In this study, ultramicroporous carbonaceous materials (UCMs) containing sub-nanometer-scale pores are fabricated using a simple in situ carbonization/activation of cellulose-based compounds containing potassium. The results show that alkali cations act as charge carriers in the ultramicropores (<0.7 nm), and these materials can deliver high capacitances of ∼300 F g-1 at 0.5 A g-1 and 130 F g-1, even at a high current rate of 65 A g-1 in an aqueous medium. In addition, the UCM-based symmetric supercapacitors are stable over 10,000 cycles and have a high energy and power densities of 8.4 Wh kg-1 and 15,000 W kg-1, respectively. This study provides a better understanding of the effects of ultramicropores in alkali cation storage.

  18. Injectable liquid alkali alloy based-tumor thermal ablation therapy. (United States)

    Rao, Wei; Liu, Jing


    The alkali metal was recently found to be a very useful agent for inducing minimally invasive tumor hyperthermia therapy. However, the solid-like metal makes it somewhat inconvenient to perform the surgery. Here, to overcome this drawback, the NaK alloy in liquid state at room temperature was proposed as a highly efficient thermal ablative agent for tumor treatment. For illustration purposes, the functionalized liquid NaK alloy at a mass ratio 1:1 was obtained and an amount of 0.35 ml was injected into in vitro pork. The sizes of the damage region and temperature response were measured. It was found that significant temperature increase by a magnitude of > 80 degrees C can easily be obtained. This produced a large coagulation and necrotic area within selected areas for in vitro tests and the necrotic region volume is three times that of the NaK injection quantity. Furthermore, for the in vivo experiment, breast EMT6 tumor in mouse was subjected to treatment by NaK alloy. Tumor was harvested after the experiment to assess its viability. Histological section showed complete necrosis at the target site. These conceptual results demonstrate that using injectable liquid alkali alloy to ablate tumor is rather promising. This study also raised interesting issues waiting for clarification in future technical and animal studies aiming to assess efficacy, side effects and safety of the new therapy.

  19. Dislocation unpinning model of acoustic emission from alkali halide crystals

    Indian Academy of Sciences (India)

    B P Chandra; Anubha S Gour; Vivek K Chandra; Yuvraj Patil


    The present paper reports the dislocation unpinning model of acoustic emission (AE) from alkali halide crystals. Equations are derived for the strain dependence of the transient AE pulse rate, peak value of the AE pulse rate and the total number of AE pulse emitted. It is found that the AE pulse rate should be maximum for a particular strain of the crystals. The peak value of the AE pulse rate should depend on the volume and strain rate of the crystals, and also on the pinning time of dislocations. Since the pinning time of dislocations decreases with increasing strain rate, the AE pulse rate should be weakly dependent on the strain rate of the crystals. The total number of AE should increase linearly with deformation and then it should attain a saturation value for the large deformation. By measuring the strain dependence of the AE pulse rate at a fixed strain rate, the time constant $_{\\text{s}}$ for surface annihilation of dislocations and the pinning time $_{\\text{p}}$ of the dislocations can be determined. A good agreement is found between the theoretical and experimental results related to the AE from alkali halide crystals.

  20. Surface modification by alkali and heat treatments in titanium alloys. (United States)

    Lee, Baek-Hee; Do Kim, Young; Shin, Ji Hoon; Hwan Lee, Kyu


    Pure titanium and titanium alloys are normally used for orthopedic and dental prostheses. Nevertheless, their chemical, biological, and mechanical properties still can be improved by the development of new preparation technologies. This has been the limiting factor for these metals to show low affinity to living bone. The purpose of this study is to improve the bone-bonding ability between titanium alloys and living bone through a chemically activated process and a thermally activated one. Two kinds of titanium alloys, a newly designed Ti-In-Nb-Ta alloy and a commercially available Ti-6Al-4V ELI alloy, were used in this study. In this study, surface modification of the titanium alloys by alkali and heat treatments (AHT), alkali treated in 5.0M NaOH solution, and heat treated in vacuum furnace at 600 degrees C, is reported. After AHT, the effects of the AHT on the bone integration property were evaluated in vitro. Surface morphologies of AHT were observed by optical microscopy (OM) and scanning electron microscopy (SEM). Chemical compositional surface changes were investigated by X-ray diffractometry (XRD), energy dispersive spectroscopy (EDS), and auger electron spectroscopy (AES). Titanium alloys with surface modification by AHT showed improved bioactive behavior, and the Ti-In-Nb-Ta alloy had better bioactivity than the Ti-6Al-4V ELI alloy in vitro.

  1. Reactive transport modeling at uranium in situ recovery sites: uncertainties in uranium sorption on iron hydroxides (United States)

    Johnson, Raymond H.; Tutu, Hlanganani; Brown, Adrian; Figueroa, Linda; Wolkersdorfer, Christian


    Geochemical changes that can occur down gradient from uranium in situ recovery (ISR) sites are important for various stakeholders to understand when evaluating potential effects on surrounding groundwater quality. If down gradient solid-phase material consists of sandstone with iron hydroxide coatings (no pyrite or organic carbon), sorption of uranium on iron hydroxides can control uranium mobility. Using one-dimensional reactive transport models with PHREEQC, two different geochemical databases, and various geochemical parameters, the uncertainties in uranium sorption on iron hydroxides are evaluated, because these oxidized zones create a greater risk for future uranium transport than fully reduced zones where uranium generally precipitates.

  2. Study on the modulating effect of polysaccharide upon the mineralization of iron hydroxide

    Institute of Scientific and Technical Information of China (English)

    HUANG Jiangbo; SUN Zhenya


    To investigate the modulating effect of polysaccharide upon the mineralization of iron hydroxide, a series of simulative biomineralization experiments using dextran and chitosan as organic substrates were conducted in this paper. The results showed that iron hydroxide gel nucleated and grew in polysaccharide molecules, with the self-assemble effect of dextran or chitosan, the nanometer-sized akaganeite was formed. The shape, size and crystal structural type of iron oxyhydroxide formed from iron hydroxide gel depend on the type of polysaccharide and its concentrations.

  3. Evaluation of layered zinc hydroxide nitrate and zinc/nickel double hydroxide salts in the removal of chromate ions from solutions (United States)

    de Oliveira, Henrique Bortolaz; Wypych, Fernando


    Layered zinc hydroxide nitrate (ZnHN) and Zn/Ni layered double hydroxide salts were synthesized and used to remove chromate ions from solutions at pH 8.0. The materials were characterized by many instrumental techniques before and after chromate ion removal. ZnHN decomposed after contact with the chromate solution, whereas the layered structure of Zn/Ni hydroxide nitrate (Zn/NiHN) and Zn/Ni hydroxide acetate (Zn/NiHA) remained their layers intact after the topotactic anionic exchange reaction, only changing the basal distances. ZnHN, Zn/NiHN, and Zn/NiHA removed 210.1, 144.8, and 170.1 mg of CrO42-/g of material, respectively. Although the removal values obtained for Zn/NiHN and Zn/NiHA were smaller than the values predicted for the ideal formulas of the solids (194.3 and 192.4 mg of CrO42-/g of material, respectively), the measured capacities were higher than the values achieved with many materials reported in the literature. Kinetic experiments showed the removal reaction was fast. To facilitate the solid/liquid separation process after chromium removal, Zn/Ni layered double hydroxide salts with magnetic supports were also synthesized, and their ability to remove chromate was evaluated.

  4. Study on the Structure and Properties of Polynosic Fiber Treated by Alkali

    Institute of Scientific and Technical Information of China (English)

    WEI Meng-yuan; XUE Wen-liang; CHENG Long-di


    The regenerated cellulose fibers, made from wood pulp, have excellent physical properties like cotton fiber. Especially polynosic fibers can be mercerized by alkali, but conventional Viscose fiber can not be treated or mercerized by alkali. The paper studies on behavior of polynosic fibers treated by alkali, including physical properties, such as weight loss, tensile strength and elongation, and fiber structures properties. In this paper, on the basis of study on polynosic fibers treated by alkali, the conclusions were drawn as following. Firstly, polynosic fiber is good at alkali resistance. Secondly, the changes of fiber structure and physical properties begin declining at 5 wt% NaOH concentration and reverse changes take place at 10 wt%.

  5. Influence of TiO2 on the Alkali Resistance and Structure of Invert Glass

    Institute of Scientific and Technical Information of China (English)

    ZHAO Qing-lin; WU Zheng-ming; BU Heng-zhi


    Through measuring the alkali resistance of the invert glass and the quantity of SiO2 and TiO2 migrating fron the glass into the solution,the influence of TiO2 on the alkali resistance of the glass is discussed and its structure is also analyzed by infrared spectroscopy.It is concluded that TiO2 has double functions for the alkali resistance of the invert glass.On the one hand ,both TiO2 polarizing the secondary ions in glass and TiO2 isomorphism replacement of SiO2 make the alkali resistance of the glass decrease.On the ther hand,TiO2 patching network and anti-erosion covering help to increase the alkali resistance.

  6. Adding nickel formate in alkali lignin to increase contents of alkylphenols and aromatics during fast pyrolysis. (United States)

    Geng, Jing; Wang, Wen-Liang; Yu, Yu-Xiang; Chang, Jian-Min; Cai, Li-Ping; Shi, Sheldon Q


    The composition of pyrolysis vapors obtained from alkali lignin pyrolysis with the additive of nickel formate was examined using the pyrolysis gas chromatography-mass spectrometry (Py-GC/MS). Characterization of bio-chars was performed using X-ray diffraction (XRD). Results showed that the nickel formate significantly increased liquid yield, simplified the types of alkali lignin pyrolysis products and increased individual component contents. The additive of nickel formate increased contents of alkylphenols and aromatics from alkali lignin pyrolysis. With an increase in temperature, a greater amount of the relative contents can be achieved. The nickel formate was thermally decomposed to form hydrogen, resulting in hydrodeoxygenation of alkali lignin during pyrolysis. It was also found that Ni is in favor of producing alkylphenols. The analysis based on the experimental result provided evidences used to propose reaction mechanism for pyrolysis of nickel formate-assisted alkali lignin.

  7. Communication: Dimensionality of the ionic conduction pathways in glass and the mixed-alkali effect. (United States)

    Novy, Melissa; Avila-Paredes, Hugo; Kim, Sangtae; Sen, Sabyasachi


    A revised empirical relationship between the power law exponent of ac conductivity dispersion and the dimensionality of the ionic conduction pathway is established on the basis of electrical impedance spectroscopic (EIS) measurements on crystalline ionic conductors. These results imply that the "universal" ac conductivity dispersion observed in glassy solids is associated with ionic transport along fractal pathways. EIS measurements on single-alkali glasses indicate that the dimensionality of this pathway D is ∼2.5, while in mixed-alkali glasses, D is lower and goes through a minimum value of ∼2.2 when the concentrations of the two alkalis become equal. D and σ display similar variation with alkali composition, thus suggesting a topological origin of the mixed-alkali effect.

  8. Illustration of alkali corrosion mechanisms in high temperature thermal insulation materials

    Energy Technology Data Exchange (ETDEWEB)

    Aneziris, C.G.; Fischer, U.; Schlegel, E. [Technical Univ. of Freiberg (Germany)


    Alkali attack is a chronic problem in the most popular high temperature applications such as blast furnaces, gasifiers, glass furnaces and cement kilns. Especially in the last years the problem of alkali corrosion is dramatically increased due to the waste burning and the combustion of the so called secondary fuels in kilns at high temperature processes. The German cement industry uses up to 100 percent of secondary fuels - a little or no coal, oil or gas- but mainly burnable waste. According to the literature destruction of the refractory can occur by the formation of low-melting low-viscosity liquids, or, more usually by the formation of dry expansive alkali-aluminosilicate compounds that result to chemical spalling. This work explores due to laboratory experiments supported partially by post mortem industrial trials the chemical interactions between alkali species and established refractory materials and illustrates four main alkali corrosion mechanisms. (orig.)

  9. First-principles study of ternary graphite compounds cointercalated with alkali atoms (Li, Na, and K) and alkylamines towards alkali ion battery applications (United States)

    Ri, Gum-Chol; Yu, Chol-Jun; Kim, Jin-Song; Hong, Song-Nam; Jong, Un-Gi; Ri, Mun-Hyok


    First-principles calculations were carried out to investigate the structural, energetic, and electronic properties of ternary graphite compounds cointercalated with alkali atoms (AM = Li, Na, and K) and normal alkylamine molecules (nCx; x = 1, 2, 3, 4), denoted as AM-nCx-GICs. From the optimization of the orthorhombic unit cells for the crystalline compounds, it was found that, with the increase in the atomic number of alkali atoms, the layer separations decrease in contrast to AM-GICs, while the bond lengths between alkali atoms and graphene layer, and nitrogen atom of alkylamine increase. The calculated formation energies and interlayer binding energies of AM-nC3-GICs indicate that the compounds is increasingly stabilized from Li to K, and the energy barriers for migration of alkali atoms suggest that alkali cation with larger ionic radius diffuses more smoothly in graphite, being similar to AM-GICs. Through the analysis of electronic properties, it was established that more extent of electronic charge is transferred from more electropositive alkali atom to the carbon ring of graphene layer, and the hybridization of valence electron orbitals between alkylamine molecules and graphene layer is occurred.

  10. Calculation of Interaction Parameters from Immiscible Phase Diagram of Alkali Metal or Alkali Earth Metal-Halide System by Means of Subregular Solution Model

    Institute of Scientific and Technical Information of China (English)


    In this paper, the interaction parameters in the subregular solution model, λ1 and λ2, are regarded as a linear function of temperature, T. Therefore, the molar excess Gibbs energy of A-B binary system may be reexpressed as follows: The calculation of the model parameters, λ11, λ12, λ21 and λ22, was carried out numerically from the phase diagrams for 11 alkali metal-alkali halide or alkali earth metal-halide systems.In addition, artificial neural network trained by known data has been used to predict the values of these model parameters. The predicted results are in good agreement with the.calculated ones. The applicability of the subregular solution model to the alkali metal-alkali halide or alkali earth metal-halide systems were tested by comparing the available experimental composition along the boundary of miscibility gap with the calculated ones which were obtained by using genetic algorithm. The good agreement between the calculated and experimental results across the entire liquidus is valid evidence in support of the model.

  11. Equilibrium Kinetics and Isotherm Studies of Cu (II Adsorption from Waste Water onto Alkali Activated Oil Palm Ash

    Directory of Open Access Journals (Sweden)

    Zaira Z. Chowdhury


    Full Text Available Problem statement: Heavy metal accumulation in waste water could affect aquatic life, human health and overall ecosystem adversely. Therefore, in recent years much emphasis has been given for the use of industrial waste material as low cost adsorbents for removal of metallic contaminants from waste water. Approach: Present study deals with the adsorption equilibrium and kinetics of Cu (II cation using sodium hydroxide activated Oil Palm Ash (OPA. Adsorption was investigated in a batch system with respect to various parameters such as initial metal ion concentration, contact time and pH of the solution. Surface characterization of the prepared adsorbent was done by using surface area analyzer, Scanning Electron Microscope (SEM and X-ray Fluorescence and compared with natural oil palm ash. The adsorption equilibrium data were best represented by Langmuir, Freundlich and Temkin model. Equilibrium kinetics studies were performed by Pseudo first order, Pseudo second order and Intra-particle diffusion. Results: Maximum monolayer adsorption capacity observed at 30°C was 18.86 mg g−1. Kinetic data correlated well with the pseudo second order model, suggesting that the adsorption process might be chemical sorption. The linear plots of intra particle diffusion revealed that the adsorption process was mainly governed by pore diffusion. Equilibrium uptake was increased with increase of initial concentration and contact time. Experimental data showed that about 96.03% of copper can be removed at pH 5.5. Conclusion: The research concluded that activation by alkali treatment of natural OPA would produce sufficient porosities and surface area and it has got good potential to remove Cu (II from waste water.

  12. The action and interaction of calcium and alkali chlorides on eggs of Limnaea stagnalis and their chemical interpretation

    NARCIS (Netherlands)

    Geilenkirchen, W.L.M.


    1. 1. The action and interaction of CaCl2 and alkali chlorides on eggs of Limnaea stagnalis have been studied. 2. 2. CaCl2 antagonizes death caused by alkali chlorides. The number of normally developing embryos increases in all cases. 3. 3. Alkali chlorides antagonize death caused by CaCl2. With NaC

  13. Ultrathin nickel hydroxide nanosheet arrays grafted biomass-derived honeycomb-like porous carbon with improved electrochemical performance as a supercapacitive material (United States)

    Nagaraju, Goli; Cha, Sung Min; Yu, Jae Su


    Three-dimensional hierarchical honeycomb-like activated porous carbon pillared ultrathin Ni(OH)2 nanosheets (Ni(OH)2 NSs@HAPC) for use as supercapacitor materials were facilely synthesized. With an aid of pine cone flowers as a biomass source, HAPC conducting scaffolds were prepared by the alkali treatment and pyrolysis methods under an inert gas atmosphere. Subsequently, the Ni(OH)2 NSs were synthesized evenly on the surface of HAPC via a solvothermal method. The resulting HAPC and Ni(OH)2 NSs@HAPC composite materials offered free pathways for effective diffusion of electrolyte ions and fast transportation of electrons when employed as an electrode material. The Ni(OH)2 NSs@HAPC composite electrode exhibited excellent electrochemical properties including a relatively high specific capacitance (Csp) value of ~ 916.4 F/g at 1 A/g with good cycling stability compared to the pristine HAPC and Ni(OH)2 NSs electrodes. Such bio-friendly derived carbon-based materials with transition metal hydroxide/oxide composite materials could be a promising approach for high-performance energy storage devices because of their advantageous properties of cost effectiveness and easy availability.

  14. Antimicrobial effect of calcium hydroxide as endo intracanal dressing on Streptococcus viridans

    Directory of Open Access Journals (Sweden)

    Nanik Zubaidah


    Full Text Available Calcium hydroxide had been used as the intra-canal dressing in endodontic treatment due to its high alkaline and antimicrobial capacity. It can also dissolve the necrotic tissue, prevent dental root resorbtion and regenerate a new hard tissue. The aim of this study was to determine the concentration of calcium hydroxide which had the highest antimicrobial effect on Streptococcus viridans. Samples were divided into 5 groups; each group consisted of 8 samples with different concentration of calcium hydroxide. Group I: 50%, group II: 55, Group III: 60%, Group IV: 65%, Group V: 70%. The antimicrobial testing was performed using diffusion method against Streptococcus viridans. The result of susceptibility test was showed by the inhibition zone diameter which measured with caliper (in millimeter. We analyzed the data using One-Way ANOVA test with significant difference 0.05 and subsequently LSD test. The study showed that calcium hydroxide with concentration 60% has the highest antimicrobial effect.

  15. A Ni-Fe Layered Double Hydroxide-Carbon Nanotube Complex for Water Oxidation

    CERN Document Server

    Gong, Ming; Wang, Hailiang; Liang, Yongye; Wu, Justin Zachary; Zhou, Jigang; Wang, Jian; Regier, Tom; Wei, Fei; Dai, Hongjie


    Highly active, durable and cost-effective electrocatalysts for water oxidation to evolve oxygen gas hold a key to a range of renewable energy solutions including water splitting and rechargeable metal-air batteries. Here, we report the synthesis of ultrathin nickel iron layered double hydroxide nanoplates on mildly oxidized multi-walled carbon nanotubes. Incorporation of Fe into the nickel hydroxide induced the formation of NiFe-layered double hydroxide. The nanoplates were covalently attached to a network of nanotubes, affording excellent electrical wiring to the nanoplates. The ultra-thin Ni-Fe layered double hydroxide nanoplates/carbon nanotube complex was found to exhibit unusually high electro-catalytic activity and stability for oxygen evolution and outperformed commercial precious metal Ir catalysts.

  16. Waste metal hydroxide sludge as adsorbent for a reactive dye. (United States)

    Santos, Sílvia C R; Vílar, Vítor J P; Boaventura, Rui A R


    An industrial waste sludge mainly composed by metal hydroxides was used as a low-cost adsorbent for removing a reactive textile dye (Remazol Brilliant Blue) in solution. Characterization of this waste material included chemical composition, pH(ZPC) determination, particle size distribution, physical textural properties and metals mobility under different pH conditions. Dye adsorption equilibrium isotherms were determined at 25 and 35 degrees C and pH of 4, 7 and 10 revealing reasonably fits to Langmuir and Freundlich models. At 25 degrees C and pH 7, Langmuir fit indicates a maximum adsorption capacity of 91.0mg/g. An adsorptive ion-exchange mechanism was identified from desorption studies. Batch kinetic experiments were also conducted at different initial dye concentration, temperature, adsorbent dosage and pH. A pseudo-second-order model showed good agreement with experimental data. LDF approximation model was used to estimate homogeneous solid diffusion coefficients and the effective pore diffusivities. Additionally, a simulated real effluent containing the selected dye, salts and dyeing auxiliary chemicals, was also used in equilibrium and kinetic experiments and the adsorption performance was compared with aqueous dye solutions.

  17. Reactions of cumene hydroperoxide mixed with sodium hydroxide. (United States)

    Hou, Hung-Yi; Shu, Chi-Min; Tsai, Tung-Lin


    Decomposition of cumene hydroperoxide (CHP) was undertaken in a free radical chain reaction. The peroxyl group is very active and unstable, while the remainder of the molecule is inert. CHP reacted with various concentrations of dilute sodium hydroxide as a catalyst to cleave at ambient and decomposition temperature. The products were verified by GC/MS, and were quantitatively analyzed by chromatography. CHP cleaved heterolytic with NaOH at 250 degrees C, whose major product was dimethylphenyl carbinol (DMPC); however, the main products become acetophenone and alpha-methylstyrene by cleaved homolytic pathway. The catalytic concentrations of NaOH significantly affected the branch ratios of DMPC under decomposition. Based on the experimental results, a radical cleavage mechanism was proposed. To sum up, the reaction parameters, such as temperature, Lewis base, etc., could affect the incompatibilities and decomposition pathways for proper CHP cleavage process. In addition, exothermic onset temperatures (T0) and heat of decomposition (Delta Hd) of incompatible mixtures and CHP itself were studied by differential scanning calorimetry (DSC). Comparisons of T0, Delta Hd and peak power were assessed to corroborate the severity of thermal hazards. From the decay rate of CHP concentration, the reaction order was determined to be 0.5, and the Arrhenius parameters were measured as Ea=92.1 kJ/mol and frequency factor A=2.42 x 10(10)min(-1).

  18. Layered-double-hydroxide-modified electrodes: electroanalytical applications. (United States)

    Tonelli, Domenica; Scavetta, Erika; Giorgetti, Marco


    Two-dimensional inorganic solids, such as layered double hydroxides (LDHs), also defined as anionic clays, have open structures and unique anion-exchange properties which make them very appropriate materials for the immobilization of anions and biomolecules that often bear an overall negative charge. This review aims to describe the important aspects and new developments of electrochemical sensors and biosensors based on LDHs, evidencing the research from our own laboratory and other groups. It is intended to provide an overview of the various types of chemically modified electrodes that have been developed with these 2D layered materials, along with the significant advances made over the last several years. In particular, we report the main methods used for the deposition of LDH films on different substrates, the conductive properties of these materials, the possibility to use them in the development of membranes for potentiometric anion analysis, the early analytical applications of chemically modified electrodes based on the ability of LDHs to preconcentrate redox-active anions and finally the most recent applications exploiting their electrocatalytic properties. Another promising application field of LDHs, when they are employed as host structures for enzymes, is biosensing, which is described considering glucose as an example.

  19. Mechanochemical synthesis of low-fluorine doped aluminum hydroxide fluorides (United States)

    Scalise, V.; Scholz, G.; Kemnitz, E.


    Different aluminum hydroxide fluorides with varying Al/F molar ratios from 1:1.5 up to 1:0.05 were successfully synthesized by mechanochemical reactions. The characterization of the products by XRD, 27Al and 19F MAS NMR, thermal analysis, nitrogen adsorption and zeta potential techniques allows a detailed understanding of the structure and surface properties of the products. Using γ-Al(OH)3 and β-AlF3·3H2O as OH- and F-sources, respectively, strongly disordered products were obtained with an Al: F molar ratio higher than 1:0.25. The fluorination degree has affected the amount of 4- and 5-fold coordinated Al sites, not present in the reactants. An evolution of the sub-coordinated Al-species has been detected also as a consequence of annealing processes. Obviously, these species affect the phase transition to alumina, by decreasing the transition temperature of the formation of α-Al2O3. Synthesis conditions (milling time, fluorination degree) play a crucial role for the product composition.

  20. Surface modification of magnesium hydroxide using vinyltriethoxysilane by dry process (United States)

    Lan, Shengjie; Li, Lijuan; Xu, Defang; Zhu, Donghai; Liu, Zhiqi; Nie, Feng


    In order to improve the compatibility between magnesium hydroxide (MH) and polymer matrix, the surface of MH was modified using vinyltriethoxysilane (VTES) by dry process and the interfacial interaction between MH and VTES was also studied. Zeta potential measurements implied that the MH particles had better dispersion and less aggregation after modification. Sedimentation tests showed that the surface of MH was transformed from hydrophilic to hydrophobic, and the dispersibility and the compatibility of MH particles significantly improved in the organic phase. Scanning electronic microscopy (SEM), Transmission electron microscopy (TEM) and X-ray powder diffraction (XRD) analyses showed that a thin layer had formed on the surface of the modified MH, but did not alter the material's crystalline phase. Fourier transform infrared (FT-IR) spectra, X-ray photoelectron spectra (XPS) and Thermogravimetric analysis (TGA) showed that the VTES molecules bound strongly to the surface of MH after modification. Chemical bonds (Sisbnd Osbnd Mg) formed by the reaction between Si-OC2H5 and hydroxyl group of MH, also there have physical adsorption effect in the interface simultaneously. A modification mechanism of VTES on the MH surface by dry process was proposed, which different from the modification mechanism by wet process.

  1. Atomistic Simulations of Uranium Incorporation into Iron (Hydr)Oxides

    Energy Technology Data Exchange (ETDEWEB)

    Kerisit, Sebastien N.; Felmy, Andrew R.; Ilton, Eugene S.


    Atomistic simulations were carried out to characterize the coordination environments of U incorporated in three Fe-(hydr)oxide minerals: goethite, magnetite, and hematite. The simulations provided information on U-O and U-Fe distances, coordination numbers, and lattice distortion for U incorporated in different sites (e.g., unoccupied versus occupied sites, octahedral versus tetrahedral) as a function of the oxidation state of U and charge compensation mechanisms (i.e., deprotonation, vacancy formation, or reduction of Fe(III) to Fe(II)). For goethite, deprotonation of first shell hydroxyls enables substitution of U for Fe(III) with a minimal amount of lattice distortion, whereas substitution in unoccupied octahedral sites induced appreciable distortion to 7-fold coordination regardless of U oxidation states and charge compensation mechanisms. Importantly, U-Fe distances of ~3.6 Å were associated with structural incorporation of U and cannot be considered diagnostic of simple adsorption to goethite surfaces. For magnetite, the octahedral site accommodates U(V) or U(VI) with little lattice distortion. U substituted for Fe(III) in hematite maintained octahedral coordination in most cases. In general, comparison of the simulations with available experimental data provides further evidence for the structural incorporation of U in iron (hydr)oxide minerals.

  2. Enhanced aerobic sludge granulation with layered double hydroxide

    Directory of Open Access Journals (Sweden)

    Jizhi Zhou


    Full Text Available Aerobic granular sludge technology has been developed for the biochemical treatment of wastewater in the present study. A fast cultivation of aerobic granular sludge was realized in Sequencing Batch Reactor (SBR, where Mg-Al layered double hydroxide (LDH was used as a carrier for granules growth. In comparison, the sludge particle size with LDH addition was bigger than those without LDH, with more than 50% of compact granular sludge >1.4 mm in size. This indicatestheLDH improved the growth ofthegranular sludge. The frequency of LDH addition had little effect on the granule growth. Moreover, the formation of granules led to the low sludge volume index (SVI and high mixed liquid suspended solids (MLSS in SBR reactor. With the formation of granular sludge, more than 80% of COD was removed in SBR reactor. The high COD removal efficiency of wastewater was observed regardless of various COD loading strength. The results suggest that the growth of granular sludge with LDH as a carrier enhanced the treatment efficiency. Therefore, our results have provided a promising way to prepare the granular sludge for wastewater treatment.

  3. Lithium adsorption on amorphous aluminum hydroxides and gibbsite

    Directory of Open Access Journals (Sweden)

    Konstantinos P. Prodromou


    Full Text Available Lithium (Li adsorption on both amorphous aluminum hydroxides and gibbsite was studied. For the amorphous Al(OH3 the adsorption was found to be pH dependent. Generally, 1.6 times more Li was adsorbed at initial pH value 8.0 compared with pH value 6.50. Gibbsite adsorbed 11.6 to 45.5 times less Li quantities compared with amorphous Al(OH3. Lithium adsorption was not depended on equilibrium times. It remained stable for all equilibrium times used. Lithium quantities extracted with 1N CH3COONH4 pH 7 , represent the physical adsorption, while the remaining Li that was adsorbed on Al(OH3, represents the chemical adsorption. During the desorption process 19% of Li extracted with NH4+, represents the physical adsorption, while the remaining 81% of Li, which was adsorbed represents the chemical adsorption. In gibbsite, 9.6% of Li represents the physical adsorption and 90.4% the chemical one. The experimental data conformed well to Freundlich isotherm equation.

  4. Defluoridation from aqueous solutions by granular ferric hydroxide (GFH). (United States)

    Kumar, Eva; Bhatnagar, Amit; Ji, Minkyu; Jung, Woosik; Lee, Sang-Hun; Kim, Sun-Joon; Lee, Giehyeon; Song, Hocheol; Choi, Jae-Young; Yang, Jung-Seok; Jeon, Byong-Hun


    This research was undertaken to evaluate the feasibility of granular ferric hydroxide (GFH) for fluoride removal from aqueous solutions. Batch experiments were performed to study the influence of various experimental parameters such as contact time (1 min-24h), initial fluoride concentration (1-100 mgL(-1)), temperature (10 and 25 degrees C), pH (3-12) and the presence of competing anions on the adsorption of fluoride on GFH. Kinetic data revealed that the uptake rate of fluoride was rapid in the beginning and 95% adsorption was completed within 10 min and equilibrium was achieved within 60 min. The sorption process was well explained with pseudo-first-order and pore diffusion models. The maximum adsorption capacity of GFH for fluoride removal was 7.0 mgg(-1). The adsorption was found to be an endothermic process and data conform to Langmuir model. The optimum fluoride removal was observed between pH ranges of 4-8. The fluoride adsorption was decreased in the presence of phosphate followed by carbonate and sulphate. Results from this study demonstrated potential utility of GFH that could be developed into a viable technology for fluoride removal from drinking water.

  5. Immobilization of Penicillin G Acylase on Calcined Layered Double Hydroxides

    Institute of Scientific and Technical Information of China (English)

    REN Ling-ling; HE Jing; Evans D. G.; DUAN Xue


    A hydrotalcite-like Mg2+/Al3+ layered double hydroxide(LDH) material was prepared by means of a modified coprecipitation method involving a rapid mixing step followed by a separate aging process. LDH calcined at 500 ℃, denoted as CLDH, was characterized by XRD, IR and BET surface area measurements. CLDH has a poor crystalline MgO-like structure with a high surface area and porosity. CLDH was used as a support for the immobilization of penicillin G acylase(PGA). The effect of varying the immobilization conditions, such as pH, contact time and the ratio of enzyme to support, on the activity of the immobilized enzyme in the hydrolysis of penicillin G has been studied. It was found that the activity of the immobilized enzyme decreased slightly with decreasing pH and reached a maximum after a contact time of 24 h. The activity of the immobilized enzyme increased with increasing the ratio of enzyme to support. It was found that the adsorption of PGA inhibited the expected reaction of CLDH with an aqueous medium to regenerate a LDH phase. Its original activity(36%) after 15 cycles of reuse of the immobilized enzyme was retained, but no further loss in the activity was observed.

  6. Thermochemistry of calcium oxide and calcium hydroxide in fluoride slags (United States)

    Chattopadhyay, S.; Mitchell, A.


    Calcium oxide activity in binary CaF2-CaO and ternary CaF2-CaO-Al2O3 and CaF2-CaO-SiO2 slags has been determined by CO2-slag equilibrium experiments at 1400 °C. The carbonate ca-pacity of these slags has also been computed and compared with sulfide capacity data available in the literature. The similarity in trends suggests the possibility of characterizing carbonate capacity as an alternative basicity index for fluoride-base slags. Slag-D2O equilibrium experi-ments are performed at 1400°C with different fluoride-base slags to determine water solubility at two different partial pressures of D2O, employing a new slag sampling technique. A novel isotope tracer detection technique is employed to analyze water in the slags. The water solubility data found show higher values than the previous literature data by an order of magnitude but show a linear relationship with the square root of water vapor partial pressure. The activity of hydroxide computed from the data is shown to be helpful in estimating water solubility in in-dustrial electroslag remelting (ESR) slags.

  7. In vivo toxicity studies of europium hydroxide nanorods in mice. (United States)

    Patra, Chitta Ranjan; Abdel Moneim, Soha S; Wang, Enfeng; Dutta, Shamit; Patra, Sujata; Eshed, Michal; Mukherjee, Priyabrata; Gedanken, Aharon; Shah, Vijay H; Mukhopadhyay, Debabrata


    Lanthanide nanoparticles and nanorods have been widely used for diagnostic and therapeutic applications in biomedical nanotechnology due to their fluorescence and pro-angiogenic properties to endothelial cells, respectively. Recently, we have demonstrated that europium (III) hydroxide [Eu(III)(OH)(3)] nanorods, synthesized by the microwave technique and characterized by several physico-chemical techniques, can be used as pro-angiogenic agents which introduce future therapeutic treatment strategies for severe ischemic heart/limb disease, and peripheral ischemic disease. The toxicity of these inorganic nanorods to endothelial cells was supported by several in vitro assays. To determine the in vivo toxicity, these nanorods were administered to mice through intraperitoneal injection (IP) everyday over a period of seven days in a dose dependent (1.25 to 125 mg kg(-1) day(-1)) and time dependent manner (8-60 days). Bio-distribution of europium elements in different organs was analyzed by inductively coupled plasma mass spectrometry (ICPMS). Short-term (S-T) and long-term (L-T) toxicity studies (mice euthanized on days 8 and 60 for S-T and L-T, respectively) show normal blood hematology and serum clinical chemistry with the exception of a slight elevation of liver enzymes. Histological examination of nanorod-treated vital organs (liver, kidney, spleen and lungs) showed no or only mild histological changes that indicate mild toxicity at the higher dose of nanorods.

  8. Methotrexate intercalated ZnAl-layered double hydroxide (United States)

    Chakraborty, Manjusha; Dasgupta, Sudip; Soundrapandian, Chidambaram; Chakraborty, Jui; Ghosh, Swapankumar; Mitra, Manoj K.; Basu, Debabrata


    The anticancerous drug methotrexate (MTX) has been intercalated into an ZnAl-layered double hydroxide (LDH) using an anion exchange technique to produce LDH-MTX hybrids having particle sizes in the range of 100-300 nm. X-ray diffraction studies revealed increases in the basal spacings of ZnAl-LDH-MTX hybrid on MTX intercalation. This was corroborated by the transmission electron micrographs, which showed an increase in average interlayer spacing from 8.9 Å in pristine LDH to 21.3 Å in LDH-MTX hybrid. Thermogravimetric analyses showed an increase in the decomposition temperature for the MTX molecule in the LDH-MTX hybrid indicating enhanced thermal stability of the drug molecule in the LDH nanovehicle. The cumulative release profile of MTX from ZnAl-LDH-MTX hybrids in phosphate buffer saline (PBS) at pH 7.4 was successfully sustained for 48 h following Rigter-Peppas model release kinetics via diffusion.

  9. Bionanocomposites based on layered double hydroxides as drug delivery systems (United States)

    Aranda, Pilar; Alcântara, Ana C. S.; Ribeiro, Ligia N. M.; Darder, Margarita; Ruiz-Hitzky, Eduardo


    The present work introduces new biohybrid materials involving layered double hydroxides (LDH) and biopolymers to produce bionanocomposites, able to act as effective drug delivery systems (DDS). Ibuprofen (IBU) and 5-aminosalicylic acid (5-ASA) have been chosen as model drugs, being intercalated in a Mg-Al LDH matrix. On the one side, the LDHIBU intercalation compound prepared by ion-exchange reaction was blended with the biopolymers zein, a highly hydrophobic protein, and alginate, a polysaccharide widely applied for encapsulating drugs. On the other side, the LDH- 5-ASA intercalation compound prepared by co-precipitation was assembled to the polysaccharides chitosan and pectin, which show mucoadhesive properties and resistance to acid pH values, respectively. Characterization of the intercalation compounds and the resulting bionanocomposites was carried out by means of different experimental techniques: X-ray diffraction, infrared spectroscopy, chemical and thermal analysis, as well as optical and scanning electron microscopies. Data on the swelling behavior and drug release under different pH conditions are also reported.

  10. Surface modification of magnesium hydroxide by γ-aminopropyltriethoxysilane

    Institute of Scientific and Technical Information of China (English)

    LUO Wei; FENG Qi-ming; OU Le-ming; LIU Kun


    Magnesium hydroxide (MH), which is commonly used as a halogen-free flame retardant filler in composite materials, was modified by silanization reaction with γ-aminopropyltriethoxysilane (γ-APS) in aqueous solution at different pH values (pH range from 8.0 to 12.0). The surface properties of grafted γ-APS on MH surface as a function of solution pH value were studied using elemental analysis, Fourier transform infrared spectroscopy and zeta potential measurement. The results show that hydrolysis and condensation of γ-APS are activated in alkaline solution and lead to multilayer adsorption of γ-APS molecules on the surface of MH. The type of adsorption orientation of γ-APS on MH surface is a function of coverage density that is altered by changing solution pH value. At low coverage density (e.g.55nm-2), γ-APS molecules are preferentially adsorbed to the surface with the silicon moiety towards the surface, and increasing coverage density (e.g.90nm-2) leads to parallel orientation. At an even higher coverage density(e.g.115nm-2), γ-APS molecules bond to the surface with the amino moiety towards the surface.

  11. Mixing Acid Salts and Layered Double Hydroxides in Nanoscale under Solid Condition



    The immobilization of potassium sorbate, potassium aspartate and sorbic acid in layered double hydroxide under solid condition was examined. By simply mixing two solids, immobilization of sorbate and aspartate in the interlayer space of nitrate-type layered double hydroxide, so called intercalation reaction, was achieved, and the uptakes, that is, the amount of immobilized salts and the interlayer distances of intercalation compounds were almost the same as those obtained in aqueous solution...

  12. Effects of aluminum hydroxide and calcium carbonate antacids on the bioavailability of ciprofloxacin.


    Frost, R W; Lasseter, K C; Noe, A J; Shamblen, E C; Lettieri, J T


    This study was designed to determine the effects of an aluminum hydroxide antacid and a calcium carbonate antacid on the bioavailability of ciprofloxacin (Cipro). Cipro (750 mg) was administered orally to 12 healthy volunteers in a three-way randomized crossover design. The three treatments included Cipro alone, four 850-mg calcium carbonate tablets taken 5 min before Cipro, and three 600-mg aluminum hydroxide tablets taken 5 min before Cipro. The relative bioavailability of Cipro when given ...

  13. Coordination Structure of Aluminum in Magnesium Aluminum Hydroxide Studied by 27Al NMR

    Institute of Scientific and Technical Information of China (English)


    The coordination structure of aluminum in magnesium aluminum hydroxide was studiedby 27Al NMR. The result showed that tetrahedral aluminum (AlⅣ) existed in magnesiumaluminum hydroxide, and the contents of AlⅣ increased with the increase of the ratio of Al/Mg andwith the peptizing temperature. AlⅣ originated from the so-called Al13 polymer with the structureof one Al tetrahedron surrounded by twelve Al octahedrons.

  14. Layered double hydroxides as containers of inhibitors in organic coatings for corrosion protection of carbon steel


    Hang, To Thi Xuan; Truc, Trinh Anh; Duong, Nguyen Thuy; Pébère, Nadine; Olivier, Marie-Georges


    International audience; The present work focuses on the use of layered double hydroxides (LDH) as containers for corrosion inhibitors in an epoxy coating. 2-Benzothiazolylthio-succinic acid (BTSA), used as corrosion inhibitor, was intercalated by co-precipitation in magnesium-aluminum layered double hydroxides. The obtained LDH-BTSA was characterized by infrared spectroscopy, X-ray diffraction and scanning electron microscopy. BTSA release from LDH-BTSA in NaCl solutions was investigated by U...

  15. Parametric Effect of Sodium Hydroxide and Sodium Carbonate on the Potency of a Degreaser

    Directory of Open Access Journals (Sweden)

    Babatope Abimbola Olufemi


    Full Text Available Normal 0 false false false EN-US X-NONE X-NONE Experimental and statistical analysis was carried out on the comparative effect of sodium hydroxide and sodium carbonate on the potency of a laboratory produced degreaser in this work. The materials used include; octadecyl benzene sulphonic acid, sodium hydroxide, sodium carbonate, sodium metasilicate, carboxyl methyl cellulose (C.M.C, formadelhyde, perfume, colourant and distilled water. Different samples of degreaser were produced with varying composition of sodium hydroxide and sodium carbonate respectively. Statistical significance through methods like analysis of variance (ANOVA of some parameters on various concentrations of sodium hydroxide and sodium carbonate was investigated. The effect of the varying compositions of sodium hydroxide and sodium carbonate was also determined by using a gray scale (GS test, and also subjecting surfaces heavily stained with crude oil to determine and characterize the cleansing action of the degreaser. It was found that as the concentration of sodium hydroxide increases, the cleansing ability also increases, whereas the increase in concentration of sodium carbonate had no effect on the cleansing ability. The work would enable production of effective, useful and property controlled degreasers at moderate cost.

  16. Adsorption of hydrated hydroxide and hydronium ions on Ag(1 1 1). A quantum mechanical investigation (United States)

    Patrito, E. M.; Paredes-Olivera, P.


    In this paper we have studied comparatively the adsorption of hydroxide and hydronium ions, extending our previous study on hydronium adsorption [J. Phys. Chem. B. 105 (2001) 7227] and emphasizing the adsorption of hydroxide. The calculations were performed on the 111 surface of silver using ab initio quantum mechanical methods (Hartree-Fock+Moller-Plesset second order perturbation theory). The adsorption was investigated for the bare and the hydrated ions (up to three water molecules). Binding energies, equilibrium structures and charge transfer processes were investigated. While the successive hydration of hydronium detaches the ion from the surface, the hydrated hydroxide anion remains specifically adsorbed. Charge transfer processes between the adsorbates and the surface were studied using electron density difference plots and effective charges obtained from Mulliken populations and from surface-dipole moment curves. The energetics of the surface reactions leading to the formation of the hydrated hydronium and hydroxide ions from the bare adsorbed ions and water molecules was also investigated. Both reactions are exothermic mainly due to the formation of strong hydrogen bonds. The effect of an external homogeneous electric field perpendicular to the surface on different adsorbate properties was investigated for the bare and hydrated hydroxide ion in order to model the environment of the electrical double layer. The electric field affects the orientation of the water molecules on the surface and the hydroxide surface distance.

  17. Cadmium hydroxide and oxide nanoporous walls with high performance photocatalytic properties

    Energy Technology Data Exchange (ETDEWEB)

    Chang, Yu-Cheng, E-mail:


    Highlights: • Cd(OH){sub 2} nanowalls were directly grown on glass substrate by hydrothermal method. • The thicknesses of Cd(OH){sub 2} nanowalls can be effectively controlled by HMTA. • Cd(OH){sub 2} and CdO nanoporous walls exhibit very strong and broad emission properties. • Cd(OH){sub 2} and CdO nanoporous walls have exhibited very effective photocatalysts. • The two mixture nanoporous walls are beneficial for optoelectronic applications. - Abstract: Cadmium hydroxide nanowalls were directly grown on glass substrate by a hydrothermal method. The concentration of hexamethylenetetramine plays a crucial role for controlling the thicknesses of cadmium hydroxide nanowalls. A part of the cadmium hydroxide nanowalls can be converted to cadmium oxide nanoporous walls by annealing cadmium hydroxide in air at 350 °C for 1 h. Cadmium hydroxide and oxide nanoporous walls exhibited very strong and broad emission properties in the cathodoluminescence spectrum. Furthermore, cadmium hydroxide and oxide nanoporous walls can also provide a higher surface-to-volume ratio to result their higher photocatalytic performance in degradation of methylene blue.

  18. Spectroscopic properties of alkali atoms embedded in Ar matrix. (United States)

    Jacquet, E; Zanuttini, D; Douady, J; Giglio, E; Gervais, B


    We present a theoretical investigation of visible absorption and related luminescence of alkali atoms (Li, Na, and K) embedded in Ar matrix. We used a model based on core polarization pseudopotentials, which allows us to determine accurately the gas-to-matrix shifts of various trapping sites. The remarkable agreement between our calculated results and the experimental spectra recorded by several authors allows us to establish a clear assignment of the observed spectra, which are made of contributions from crystalline sites on the one hand, and of grain boundary sites on the other hand. Our study reveals remarkably large Stokes shifts, up to 9000 cm(-1), which could be observed experimentally to identify definitely the trapping sites.

  19. The Effect of Radiation "Memory" in Alkali-Halide Crystals (United States)

    Korovkin, M. V.; Sal'nikov, V. N.


    The exposure of the alkali-halide crystals to ionizing radiation leads to the destruction of their structure, the emergence of radiation defects, and the formation of the electron and hole color centers. Destruction of the color centers upon heating is accompanied by the crystal bleaching, luminescence, and radio-frequency electromagnetic emission (REME). After complete thermal bleaching of the crystal, radiation defects are not completely annealed, as the electrons and holes released from the color centers by heating leave charged and locally uncompensated defects. Clusters of these "pre centers" lead to electric microheterogeneity of the crystal, the formation of a quasi-electret state, and the emergence of micro-discharges accompanied by radio emission. The generation of REME associated with residual defectiveness, is a manifestation of the effect of radiation "memory" in dielectrics.

  20. Electrochemical synthesis of alkali-intercalated iron selenide superconductors (United States)

    Shen, Shi-Jie; Ying, Tian-Ping; Wang, Gang; Jin, Shi-Feng; Zhang, Han; Lin, Zhi-Ping; Chen, Xiao-Long


    Electrochemical method has been used to insert K/Na into FeSe lattice to prepare alkali-intercalated iron selenides at room temperature. Magnetization measurement reveals that KxFe2Se2 and NaxFe2Se2 are superconductive at 31 K and 46 K, respectively. This is the first successful report of obtaining metal-intercalated FeSe-based high-temperature superconductors using electrochemical method. It provides an effective route to synthesize metal-intercalated layered compounds for new superconductor exploration. Project supported by the National Natural Science Foundation of China (Grant Nos. 51322211and 91422303), the Strategic Priority Research Program (B) of the Chinese Academy of Sciences (Grant No. XDB07020100), Beijing Nova Program of China (Grant No. 2011096), and K. C. Wong Education Foundation, Hong Kong, China.

  1. Structure and energetics of helium films on alkali substrates (United States)

    Boninsegni, Massimo; Szybisz, Leszek


    Low-temperature adsorption of He4 films on Alkali metal substrates is investigated theoretically by means of ground-state quantum Monte Carlo simulations. The most accurate potentials currently available are utilized to model the interaction of He4 atoms with the substrate. Continuous growth of film thickness as a function of chemical potential is observed on Li, Na, and K substrates. A superfluid monolayer forms on a Li substrate; on Na and K, thermodynamically stable films are a few layers thick. The uncertainties of the calculation and in the potentials, preclude a definitive conclusion on the existence of a stable He4 film on Rb. A comparison of the results of this calculation with those obtained using the Orsay-Trento density functional shows broad quantitative agreement.


    Institute of Scientific and Technical Information of China (English)



    We propose a dark gravito-optical dipole trap, for alkali atoms, consisting of a blue-detuned, pyramidal-hollow laser beam propagating upward and the gravity field. When cold atoms from a magneto-optical trap are loaded into the pyramidal-hollow beam and bounce inside the pyramidal-hollow beam, they experience efficient Sisyphus cooling and geometric cooling induced by the pyramidal-hollow beam and the weak repumping beam propagating downward. Our study shows that an ultracold and dense atomic sample with an equilibrium 3D momentum of ~ 3hk and an atomic density above the point of Bose-Einstein condensation may be obtained in this pure optical trap.

  3. Reclamation and Management of Saline and Alkali Soils

    DEFF Research Database (Denmark)

    Singh, Anoop; Katiyar, D.; Agrawal, S.B.


    Soil is the most precious natural resource and thus requires proper management. Estimates show that the world as a whole is losing at least 3.0 ha of arable land every minute due to salinization or sodification. In India about 7.0 M ha land is affected by salinity and alkalinity. The problem...... to combat with the problem. The present review is an attempt to emphasize the problem of salinity and alkalinity of soils, its effect on plants and application of physical, chemical and biological methods of soil reclamation along with management issues...... of saline and alkali soils is old but its magnitude and intensity have been increasing because of poor land and water management practices. The proper land management by way of its reclamation involves physical, chemical and biological means, which are site specific and their integration is highly desirable...

  4. Effect of Cross Linking Agent on Alkali/Surfactant/Polymer

    Institute of Scientific and Technical Information of China (English)

    ZHANG,Ke; LU,Xiang-Guo


    Alkali/surfactant/polymer (ASP) multisystem flooding technique, which has an expansive application prospect,is one of the enhancing oil recovery (EOR) methods. By adding the organic chromium to the ASP, the molecular structure of polymer was made to change, and the capability of controlling mobility coefficient of ASP was improved. The results showed that multisystem could still keep ultra-low interfacial tension between the multisystem and crude oil after addition of Cr3+. The resistance factor and residual resistance factor, the indicator which describes the capability of controlling mobility, upgraded strikingly. However its storage modulus and loss modulus,the indicator which describes viscoelasticity, increased. The results of physical simulation experiment indicated that this type of improved ASP could increase the recovery ratio by 4.3% compared to common ASP multisystem.

  5. 3718-F Alkali Metal Treatment and Storage Facility Closure Plan

    Energy Technology Data Exchange (ETDEWEB)



    Since 1987, Westinghouse Hanford Company has been a major contractor to the U.S. Department of Energy-Richland Operations Office and has served as co-operator of the 3718-F Alkali Metal Treatment and Storage Facility, the waste management unit addressed in this closure plan. The closure plan consists of a Part A Dangerous waste Permit Application and a RCRA Closure Plan. An explanation of the Part A Revision (Revision 1) submitted with this document is provided at the beginning of the Part A section. The closure plan consists of 9 chapters and 5 appendices. The chapters cover: introduction; facility description; process information; waste characteristics; groundwater; closure strategy and performance standards; closure activities; postclosure; and references.

  6. Experimental study of the diode pumped alkali laser (DPAL) (United States)

    Endo, Masamori; Nagaoka, Ryuji; Nagaoka, Hiroki; Nagai, Toru; Wani, Fumio


    A small-scale cesium diode-pumped alkali laser (DPAL) apparatus has been developed for fundamental researches. A commercial laser diode with volume Bragg grating outcoupler is used to pump the gain cell longitudinally. Both windows of the gain cell are set at Brewster's angle for minimum loss and maximum durability. Output coupling coefficient is continuously variable from 13% to 85% by the slanted quartz plate outcoupler inserted in the optical resonator. Small signal gain is measured with a laser diode probe at various gain cell temperatures. A 6.5 W continuouswave output with 56% optical-to-optical conversion efficiency (based on the absorbed power) has been achieved. A numerical simulation code is developed and its calculation results are in good agreement with the experiments.

  7. Strong Turbulence in Alkali Halide Negative Ion Plasmas (United States)

    Sheehan, Daniel


    Negative ion plasmas (NIPs) are charge-neutral plasmas in which the negative charge is dominated by negative ions rather than electrons. They are found in laser discharges, combustion products, semiconductor manufacturing processes, stellar atmospheres, pulsar magnetospheres, and the Earth's ionosphere, both naturally and man-made. They often display signatures of strong turbulence^1. Development of a novel, compact, unmagnetized alkali halide (MX) NIP source will be discussed, it incorporating a ohmically-heated incandescent (2500K) tantulum solenoid (3cm dia, 15 cm long) with heat shields. The solenoid ionizes the MX vapor and confines contaminant electrons, allowing a very dry (electron-free) source. Plasma densities of 10^10 cm-3 and positive to negative ion mass ratios of 1 Fusion 4, 91 (1978).

  8. Radioluminescence of synthetic quartz related to alkali ions

    Energy Technology Data Exchange (ETDEWEB)

    Martini, M., E-mail: [Dipartimento di Scienza dei Materiali, Universita degli Studi di Milano Bicocca, Via Cozzi 53, I-20125 Milano (Italy); INFN-Sezione di Milano Bicocca, Via Cozzi 53, I-20125 Milano (Italy); Fasoli, M. [Dipartimento di Scienza dei Materiali, Universita degli Studi di Milano Bicocca, Via Cozzi 53, I-20125 Milano (Italy); Galli, A. [Dipartimento di Scienza dei Materiali, Universita degli Studi di Milano Bicocca, Via Cozzi 53, I-20125 Milano (Italy); Istituto di Fotonica e Nanostrutture, IFN-CNR (Italy); Villa, I. [Dipartimento di Scienza dei Materiali, Universita degli Studi di Milano Bicocca, Via Cozzi 53, I-20125 Milano (Italy); Guibert, P. [IRAMAT-CRP2A (Institut de recherche sur les Archeomateriaux), UMR no. 5060, CNRS-Universite Bordeaux III, F-33607 Pessac (France)


    The radioluminescence (RL) of synthetic quartzes (GEMMA Quartz and Crystal Company) has been measured at room temperature. Some samples were treated by electrodiffusion ('sweeping') in order to change the concentrations of alkali ions, mainly Li{sup +} and Na{sup +}, which in quartz are known to be linked to Al ions, substitutional for Si ions. The RL emission spectra show evidence of a role of alkali ions in affecting some specific emissions. All the spectra could be analysed as composed of four bands in the blue and UV region. Specifically, the well known blue emission at around 470 nm was seen to be composed by two bands at 430 nm (2.86 eV) and at 485 nm (2.53 eV). Effects of irradiation, during the RL measurements, were clearly seen only in the 'Li swept in' sample, namely an increase in the 485 nm band intensity and a decrease in the 430 nm band one. The previously reported UV emission was detected at 355 nm (3.44 eV) in all the samples, being the most intense band in the 'swept out' sample. A further UV emission was detected at 315 nm (3.94 eV), more intense in untreated samples. Possible assignments of the detected emission bands are discussed in relation to the defects of quartz, specifically focusing on the Al centres that are most affected by sweeping procedures. - Highlights: Black-Right-Pointing-Pointer Contribution to the understanding of relationships between defects in quartz and luminescence emissions. Black-Right-Pointing-Pointer Role of charge compensators at substitutional Al sites in the optical properties of quartz. Black-Right-Pointing-Pointer Evidence of the double nature of the 'blue emission' (around 470 nm).

  9. The Structure and Thermodynamics of Alkali Halide Vapors. (United States)

    Hartley, John George

    A comprehensive set of electron diffraction experiments were performed on 16 of the alkali halides in the vapor phase. A 40kev electron beam was scattered from the vapor effusing out of the nozzle of a temperature controlled gas cell. The resulting data were analyzed at the University of Edinburgh with the program ED80. This resulted in values for the bond lengths of monomers and the dimers, the bond angle of the dimers and the monomer-dimer ratios. In several cases, it was possible to further refine the data to obtain information on the mean amplitudes of vibration. As a check on the accuracy of the results, the monomer bond distances obtained by electron diffraction were compared to values obtained previously by microwave spectroscopy. The average monomer bond length r_{a} is corrected to obtain the equilibrium bond distance r_{e}. This value is then compared to the value of r_{e } obtained from microwave spectroscopy and found to be in excellent agreement. The bond lengths and angles of the dimers were compared against model calculations. While no one model was found to accurately predict the dimer structure parameters of all of the alkali halides, the Rittner model of Gowda et al was found to accurately predict the structure of six of the dimers. Thermodynamical calculations were performed on the model data which resulted in theoretical curves of the monomer-dimer ratios. Comparison of these curves with the experimental monomer-dimer ratio permits an evaluation of the model vibration frequencies. The enthalpy of formation of the dimer, Delta H_sp{2}{f}(298) is examined with regard to the size of the variation necessary to bring about agreement of the experimental and model monomer-dimer ratios.

  10. Inhibitory Effects of Mistletoe Alkali on Salivary Adenoid Cystic Carcinoma Cells

    Institute of Scientific and Technical Information of China (English)

    LI Mei-hua; WANG Yi-shu; ZHOU Hong-lan; LI Ya-juan; QIU Xin-ru; WANG Xue-yao; ZHAO Yu-yang


    Mistletoe alkali plays an important role in salivary adenoid cystic carcinoma(SACC) cell proliferation,apoptosis and invasion.Mistletoe alkali shows potent anticaner property.In this paper,immunocytochemical and immunofluorescence staining were employed to evaluate the expression levels of proliferating cell nuclear antigen(PCNA),Caspase 3,Caspase 8 and Caspase 9.Apoptosis was detected by acridine orange/ethidium bromide (AO/EB) staining,cell invasion ability was assessed by Boyden Chamber assay.Pretreatment with mistletoe alkali markedly decreased PCNA expression in SACC cells in a dose-dependent manner(P<0.001) and also led to increase the expression of Caspase 3,Caspase 8 and Caspase 9 in SACC cells compared with control group(P<0.001).Number of apoptotic cells increased dramatically in mistletoe alkali group(P<0.001).In Boyden Chamber assay,mistletoe alkali treatment could inhibit SACC cells to penetrate the artificial basement membrane compared with control group(P<0.01).Mistletoe alkali remarkably inhibited the proliferation and invasion of SACC cells and induced the apoptosis of SACC cells.These results provide an insight into the mechanisms of anticancer effects of mistletoe alkali,and highlight the potential clinical application of it.

  11. Alkali-metal-supported bismuth polyhedra-principles and theoretical studies. (United States)

    Monakhov, Kirill Yu; Linti, Gerald; Wolters, Lando P; Bickelhaupt, F Matthias


    We have quantum chemically investigated the structure, stability, and bonding mechanism in highly aggregated alkali-metal salts of bismuthanediide anions [RBi](2-) using relativistic density functional theory (DFT, at ZORA-BP86/TZ2P) in combination with a quantitative energy decomposition analysis (EDA). Our model systems are alkali-metal-supported bismuth polyhedra [(RBi)(n)M(2n-4)](4-) with unique interpenetrating shells of a bismuth polyhedron and an alkali-metal superpolyhedron. Furthermore, we have analyzed the trianionic inclusion complexes [M'@{(RBi)(n)M(2n-4)}](3-) involving an additional endohedral alkali-metal ion M'. The main objective is to assist the further development of synthetic approaches toward this class of compounds. Our analyses led to electron-counting rules relating, for example, the number of bonding orbitals (N(bond)) of the cage molecules [(RBi)(n)M(2n+Q)](Q) to the number of bismuth atoms (n(Bi)), alkali-metal atoms (n(M)), and net charge Q as N(bond) = n(Bi) + n(M) - Q (R = one-electron donor ligand; M = alkali metal; n = 4-12; Q = -4, -6, -8). Finally, on the basis of our findings, we predict the next members in the 5-fold symmetrical row of alkali-metallobismaspheres with a macroicosahedral arrangement.

  12. Alkali extraction and in vitro antioxidant activity of Monascus mycelium polysaccharides. (United States)

    Wang, Pengrong; Chen, Danfeng; Jiang, Donghua; Dong, Xiameng; Chen, Panpan; Lin, Yaoxue


    In the present work, alkali extraction technology was used to optimize the extraction of Monascus mycelium polysaccharides for the first time. The extracting parameters of alkali extracted Monascus mycelium polysaccharides were optimized by Box-Behnken design (BBD). The optimum conditions were extraction temperature 49 °C, alkali concentration 7%, solvent/material ratio 23:1 (ml/g) and extraction time 2.3 h with an enhanced yield of 10.1%, compared with the yield 4.76% of hot water extraction, indicating that alkali extraction is a more efficient way. In order to discuss the biological activity of alkali extracted polysaccharides, we compared the in vitro antioxidant activity of alkali extracted polysaccharides (AMP) with hot water extracted polysaccharides (HMP). The result showed that AMP have the similar capability of scavenging both superoxide radical and 2, 2-diphenyl-1-picrylhydrazyl (DPPH) radical of HMP in vitro. Therefore, alkali extraction technology is not only a high-efficiency way to extract AMP, but also can retain the natural antioxidant activities of AMP, which can be used in pharmaceutical and food industries.

  13. Saline-alkali land in the Yellow River Delta:amelioration zonation based on GIS

    Institute of Scientific and Technical Information of China (English)


    Soil salinization is one of the major land degradation types andhas greatly influenced sustainable agricultural development. Zonation of saline-alkali land is the precondition for effective amelioration. The present situation of saline-alkali land is monitored by remote sensing image processing. Causes for land salinization are analyzed, especially the two key factors, ground water depth and its mineralization degree, are analyzed by using long-term observation data. Previously,zonation of saline-alkali soil was made descriptively and artificially. Based on the present situation of saline-alkali land, ground water depth and ground water mineralization degree, the zonation of salinealkali land for amelioration in the Yellow River Delta was completed quantitatively. Four different ypes of saline-alkali land amelioration zones are delineated, namely, easy ameliorated zone,elatively difficult ameliorated zone, difficult ameliorated zone and unfavorable ameliorated zone.Countermeasures for ameliorating saline-alkali soils are put forward according to ecological conditions of different saline-alkali land zones.

  14. Origin of alkali rocks in the light of data on the fluid mantle flow

    Energy Technology Data Exchange (ETDEWEB)

    Kushev, V.G.; Mironov, A.G.


    The hypotheses on the alkali-basic melts as formed through partial fusion of either the hydroxyl-containing alkali peridotite (or pyroxenite), or the phlogopite- or amphibole-enriched rocks in the mantle turn out most relevant as for the alkali rock peculiarities. Still, the hypotheses do not explain the appearance of alkalies and water involved in fusion. It is supposed that the alkalies-enriched rocks result from the dynamometamorphic segregation of the mantle fluid (CH/sub 4/, H/sub 2/, CO), which reacts with the mantle rocks (magnetite+olivine+pyroxene) with subsequent release of H/sub 2/O and liberation of K and Na from the gaseous phase and pyroxenes lattice. The start of fusion is induced by sharp decrease of pressure and heat incoming along the deep dislocation zones in the mantle. Once produced, the alkali melt evolved through differetiation or interaction with enclosing rocks. This method provides interpretation of most petrological and geochemical peculiarities of different series of alkali rocks. 65 references.

  15. Effect of alkali and heat treatments for bioactivity of TiO{sub 2} nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Seo young, E-mail: [Dept. of Dental Biomaterials and Institute of Bio degradable material, Institute of Oral Bioscience and BK21 plus project, School of Dentistry, Chonbuk National University, Jeonju, 561-756 (Korea, Republic of); Kim, Yu kyoung, E-mail: [Dept. of Dental Biomaterials and Institute of Bio degradable material, Institute of Oral Bioscience and BK21 plus project, School of Dentistry, Chonbuk National University, Jeonju, 561-756 (Korea, Republic of); Park, Il song, E-mail: [Division of Advanced Materials Engineering, Research Center for Advanced Materials Development and Institute of Biodegradable Materials, Chonbuk National University, Jeonju 561-756 (Korea, Republic of); Jin, Guang chun, E-mail: [Oral Medical College, Beihua University, Jilin City 132013 (China); Bae, Tae sung, E-mail: [Dept. of Dental Biomaterials and Institute of Bio degradable material, Institute of Oral Bioscience and BK21 plus project, School of Dentistry, Chonbuk National University, Jeonju, 561-756 (Korea, Republic of); Lee, Min ho, E-mail: [Dept. of Dental Biomaterials and Institute of Bio degradable material, Institute of Oral Bioscience and BK21 plus project, School of Dentistry, Chonbuk National University, Jeonju, 561-756 (Korea, Republic of)


    Highlights: • TiO{sub 2} nanotubes formed via anodization were treated by alkali and heat. • The surface roughness was increased after alkali treatment (p < 0.05). • After alkali and heat treatment, the wettability was better than before treatment. • Alkali treated TiO{sub 2} nanotubes were shown higher HAp formation in SBF. • Heat treatment affected on the attachment of cells for alkali treated nanotubes. - Abstract: In this study, for improving the bioactivity of titanium used as an implant material, alkali and heat treatments were carried out after formation of the nanotubes via anodization. Nanotubes with uniform length, diameter, and thickness were formed by anodization. The alkali and heat-treated TiO{sub 2} nanotubes were covered with the complex network structure, and the Na compound was generated on the surface of the specimens. In addition, after 5 and 10 days of immersion in the SBF, the crystallized OCP and HAp phase was significantly increased on the surface of the alkali-treated TiO{sub 2} nanotubes (PNA) and alkali and heat-treated TiO{sub 2} nanotubes (PNAH) groups. Cell proliferation was decreased due to the formation of amorphous sodium titanate (Na{sub 2}TiO{sub 3}) layer on the surface of the PNA group. However, anatase and crystalline sodium titanate were formed on the surface of the PNAH group after heat treatment at 550 °C, and cell proliferation was improved. Thus, PNA group had higher HAp forming ability in the simulated body fluid. Additional heat treatment affected on enhancement of the bioactivity and the attachment of osteoblasts for PNA group.

  16. Use of precalciners to remove alkali from raw materials in the cement industry. Final report, July 1978-July 1980

    Energy Technology Data Exchange (ETDEWEB)

    Gartner, E.M.


    The objective of this work was to develop an efficient means of removing alkali metal compounds (alkalies) from high-alkali aluminosilicate raw materials of the type commonly used as part of cement raw mixes in order to increase the energy efficiency of cement manufacture. The intention of this project was to determine whether the high-alkali raw materials could be pyroprocessed separately to remove the alkalies before they entered the rotary kiln, where they would be mixed with the other raw feed components. If this could be achieved, considerable savings could be made in the energy required to remove alkalies, compared to conventional methods in which the cement raw mix must be treated as a whole. Two different methods of alkali removal were examined, namely, vaporization of alkalies at relatively low temperatures; and alkali-rich melt separation at relativey high temperatures. The results showed that the removal of alkalies by pyroprocessing of high-alkali raw feed components separate from the other cement raw mix components is not likely to be a practical alternative to the best available conventional precalciner technology. (LCL)

  17. Communication: Dopant-induced solvation of alkalis in liquid helium nanodroplets (United States)

    Renzler, Michael; Daxner, Matthias; Kranabetter, Lorenz; Kaiser, Alexander; Hauser, Andreas W.; Ernst, Wolfgang E.; Lindinger, Albrecht; Zillich, Robert; Scheier, Paul; Ellis, Andrew M.


    Alkali metal atoms and small alkali clusters are classic heliophobes and when in contact with liquid helium they reside in a dimple on the surface. Here we show that alkalis can be induced to submerge into liquid helium when a highly polarizable co-solute, C60, is added to a helium nanodroplet. Evidence is presented that shows that all sodium clusters, and probably single Na atoms, enter the helium droplet in the presence of C60. Even clusters of cesium, an extreme heliophobe, dissolve in liquid helium when C60 is added. The sole exception is atomic Cs, which remains at the surface.

  18. Field emission properties of capped carbon nanotubes doped by alkali metals:a theoretical investigation

    Institute of Scientific and Technical Information of China (English)

    Jin Lei; Fu Hong-Gang; Xie Ying; Yu Hai-Tao


    The electronic structures and field emission properties of capped CNT55 systems with or without alkali metal atom adsorption were systematically investigated by density functional theory calculation.The results indicate that the adsorption of alkali metal on the center site of a CNT tip is energetically favorable.In addition,the adsorption energies increase with the introduction of the electric field.The excessive negative charges on CNT tips make electron emittance much easier and result in a decrease in work function.Furthermore,the inducing effect by positively charged alkali metal atoms can be reasonably considered as the dominant reason for the improvement in field emission properties.

  19. Pretreatment of garden biomass by alkali-assisted ultrasonication: effects on enzymatic hydrolysis and ultrastructural changes


    Gabhane, Jagdish; William, SPM Prince; Vaidya, Atul Narayan; Anand, Duraisamy; Wate, Satish


    The present investigation aims at studying the effectiveness of alkali-assisted ultrasonication on pretreatment of garden biomass (GB). Dry and powdered GB suspended in 1% NaOH was ultrasonicated for 15, 30 and 60 minutes at a frequency of 25 KHZ. The mode of action and effectiveness of alkali-assisted ultrasonication on GB was established through microscopic, scanning electron microscopic and X-ray diffraction studies. A perusal of results showed that alkali-assisted ultrasonication led to f...

  20. Alkali extraction and in vitro antioxidant activity of Monascus mycelium polysaccharides


    Wang, Pengrong; Chen, Danfeng; Jiang, Donghua; Dong, Xiameng; Chen, Panpan; Lin, Yaoxue


    In the present work, alkali extraction technology was used to optimize the extraction of Monascus mycelium polysaccharides for the first time. The extracting parameters of alkali extracted Monascus mycelium polysaccharides were optimized by Box-Behnken design (BBD). The optimum conditions were extraction temperature 49 °C, alkali concentration 7%, solvent/material ratio 23:1 (ml/g) and extraction time 2.3 h with an enhanced yield of 10.1%, compared with the yield 4.76% of hot water extraction...

  1. Effect of Alkali Treatment on the Structure and Catalytic Properties of ZSM-5 Zeolite

    Institute of Scientific and Technical Information of China (English)

    Zi Yun LI; Xin SUN; Qiang XIAO; Shou He XIANG


    Catalytic properties of ZSM-5 zeolite samples pretreated with NaOH solution have been investigated. The samples are characterized by XRD, SEM, chemical analysis, and N2 adsorption.The results indicate that mesopores are created in ZSM-5 crystals under alkali treatment without change the microporous structure and acidic strength of the zeolite, but the crystallinity is greatly decreased under severe treatment. IR indicates that the concentration of silanol is greatly enriched by alkali treatment. The etherification activities of ZSM-5 zeolites are greatly increased by alkali-treatment. The noticeably improved catalytic activity of treated samples is ascribed to the formation of mesopores and greatly enriched silanol group.

  2. Trace Element Geochemistry of Hannuoba Ultramafic Inclusion—bearing Alkali Basalts

    Institute of Scientific and Technical Information of China (English)



    Presented in this paper are the trace element abundances of 16 samples of Hannuoba ultramafic inclusion-bearing aldali basalts,which were determined by instrumental neutron activation analysis and X-ray fluorescence spectrometry.The Petrogenesis of the alkali basalt suite has been modeled by batch partial melting and and Rayleigh fractional crystallization processes,The geochemical characteristics of the mantle source from where alkali basalts were derived are described in terms of variations in trace element abundances of the alkali basalt suite.

  3. Behavior of Alkali Metals and Ash in a Low-Temperature Circulating Fluidized Bed (LTCFB) Gasifier

    DEFF Research Database (Denmark)

    Narayan, Vikas; Jensen, Peter Arendt; Henriksen, Ulrik Birk


    A low-temperature circulating fluidized bed system (LTCFB) gasifier allows for pyrolysis and gasification to occurat low temperatures, thereby improving the retention of alkali and other inorganic elements within the system and minimizingthe amount of ash species in the product gas. In addition......, the low reactor temperature ensures that high-alkali biomass fuels canbe used without risk of bed defluidization. This paper presents the first investigation of the fate of alkali metals and ash in lowtemperaturegasifiers. Measurements on bed material and product gas dust samples were made on a 100 k...

  4. Production of Potassium and Calcium Hydroxide, Compost and Humic Acid from Sago (Metroxylon sagu Waste

    Directory of Open Access Journals (Sweden)

    C. P. Auldry


    Full Text Available Problem statement: Agriculture waste such as Sago Waste (SW has a potential to cause pollution when the waste is discarded into rivers. In order to add value to SW, a study was conducted to produce potassium and calcium hydroxide, compost and Humic Acid (HA from SW. Approach: The SW was air-dried and some grinded. The grinded SW was incinerated at 600°C. Potassium and calcium hydroxide was extracted by dissolving the ash in distilled water at a ratio of 1:500 (ash: water, equilibrated for 24 h at 150 rpm using a mechanical shaker and filtered. The ungrinded SW was used for compost production. The compost was produced by mixing SW (80% + chicken feed (10% + chicken dung slurry (5% + molasses (5%. Results: The hydroxide extracted from ash of SW was used to isolate HA of composted SW. The molarity and pH of the hydroxide were 0.002M and 10 respectively. Calcium (42.88 mg kg-1 and potassium (29.51 mg kg-1 content were high in the hydroxide compared with other elements. The compost took about 60 days to mature. There was an increased in pH, ash, Cation Exchange Capacity (CEC and HA and a decreased in temperature, C/N ratio, C/P ratio and organic matter. The hydroxide was able to extract 1% of HA from the composted SW. A comparison between the yields of HA extracted from the composted SW using the hydroxide of the SW and that of the analytical grade showed no statistically difference. The chemical characteristics of HA from the composted SW were in standard range. Conclusion: Potassium and calcium hydroxide, compost and HA can be produced from sago waste. Low morality of the hydroxide is able to produce good quality of HA from composted sago waste. The HA can be reconstituted with K and Ca from potassium and calcium hydroxide to produce K-Ca-humate and this needs to be investigated as a form of organic based fertilizer.

  5. Development of polymer nanocomposites based on layered double hydroxides

    Directory of Open Access Journals (Sweden)

    Sipusic, J.


    Full Text Available Polymeric nanocomposites are commonly considered as systems composed of a polymeric matrix and - usually inorganic - filler. The types of nanofillers are indicated in Fig. 1. Beside wellknown layered silicate fillers, recent attention is attracted to layered double hydroxide fillers (LDH, mainly of synthetic origin. The structure of LDH is based on brucite, or magnesium hydroxide, Mg(OH2 and is illustrated in Fig. 2. The modification of LDHs is commonly done by organic anions, to increase the original interlayer distance and to improve the organophilicity of the filler, keeping in mind their final application as fillers for, usually hydrophobic, polymer matrices. We have used the modified rehydration procedure for preparing organically modified LDH. The stoichiometric quantities of Ca33Al2O6, CaO and benzoic (B (or undecenoic (U acid were mixed with water and some acetone. After long and vigorous shaking, the precipitated fillers were washed, dried and characterized. X-ray diffraction method (XRD has shown the increase of the original interlayer distance for unmodified LDH (OH–-saturated of 0.76 nm to the 1.6 nm in LDH-B or LDH-U fillers (Fig. 3. Infrared spectroscopy method (FTIR has confirmed the incorporation of benzoic anion within the filler layers (Fig. 4. For the preparation of LDH-B and LDH-U composites with polystyrene (PS, poly(methyl methacrylate (PMMA and copolymer (SMMA matrices, a two-step in situ bulk radical polymerization was selected (Table 1 for recipes, azobisisobutyronitrile as initiator, using conventional stirred tank reactor in the first step, and heated mold with the movable wall (Fig. 6 in the second step of polymerization. All the prepared composites with LDH-U fillers were macroscopically phase-separated, as was the PMMA/LDH-B composite.PS/LDH-B and SMMA/LDH-B samples were found to be transparent and were further examined for deduction of their structure (Fig. 5 and thermal properties. FTIR measurements showed that

  6. Form and stability of aluminum hydroxide complexes in dilute solution (United States)

    Hem, John David; Roberson, Charles Elmer


    Laboratory studies of solutions 4.53 x 10 -4 to 4.5 x 10 -5 molal (12.2-1.2 ppm) in aluminum, in 0.01 molal sodium perchlorate, were conducted to obtain information as to the probable behavior of aluminum in natural water. When the solutions were brought to pH 7.5-9.5 and allowed to stand for 24 hours, a precipitate was obtained which was virtually amorphous as shown by X-rays, and which had a solubility equivalent to that of boehmite. This precipitate had a hydrolysis constant (*Ks4) of 1.93 x 10 -13a. When solutions were allowed to stead at this pH range for 10 days, their precipitates gave the X-ray pattern of bayerite (*Ks4 = 1.11 > (10- 4). These hydrolysis constants were obtained at 25?C. and corrected to zero ionic strength and are in close agreement with other published values. The predominant dissolved form in this pH range is Al(OH) -4. Below neutral pH (7.0) the dissolved aluminum species consist of octahedral units in which each aluminum ion is surrounded by six water molecules or hydroxide ions. Single units such as Al(OH2)6 + 3 and AlOH(OH2)5+2 are most abundant below pH 5.0, and where the molar ratio (r) of combined hydroxide to total dissolved aluminum is low. When r is greater than 1.0, polymerization of the octahedral units occurs. When r is between 2.0 and 3.0, solutions aged for 10 days or more contained colloidal particles between 0.10 and 0.45 ? in diameter. Particles whose diameters were greater than 0.10 ? were identified by X-ray diffraction as gibbsite. Particles smaller than 0.10 ? were also present and were shown by means of the electron microscope to have a hexagonal crystal pattern. Structured material consisting of sheets of coalesced six-membered rings of aluminum ions held together by double OH bridges has a distinctive kinetic behavior. This property was used to determine amounts of polymerized material in solutions having r between 1.0 and 3.0 after aging times ranging from a few hours to more than 4 months. Aging increased the

  7. Preferential Intercalation of Pyridinedicarboxylates into Layered Double Hydroxides

    Institute of Scientific and Technical Information of China (English)

    李蕾; 莫丹; 陈大舟


    Intercalation of 2,3-,2,4-,2,5-,2,6-,3,4-,or3,5-pyridincdicarboxylate into the layered double hydroxide (LDH),[Mg0.73AIo.27(OH)2](CO3)0.14*1.34H2O was carried out by the reconstruction method in the molar ratio of organic acid: calcined LDH=3:8, in 80% alcoholic aqueous solution at 70℃. Selective reaction was observed in com-petitive experiments involving an equal concentration pairs of acids. The preference order of the organic acids intercalated into the Mg-Al-LDH was found to be in the order of 2,3-pyridinedicarboxylate>2,5-pyridinedicarboxylate>2,4-pyridinedicarboxylate>3,5-pyridinedicarboxylate>3,4-pyridinedicarboxylate>2,6-pyridinedic arboxylate. The structures of the intercalates formed by the reaction of six guests with Mg-Al-LDH were characterized by X-ray diffraction, infrared and thermogravimetry techniques. And the charge density on the oxygens of each of the carboxylate groups for the six anions was investigated utilizing ab initio (HF/6-31G) method by G98w. From the X-ray diffraction data, the guest size and the charge density of the oxygens of the guest, the orientation of 2,3-,2,4-,2,5-,2,6-,3,4-, or 3,5-pyridinedicarboxylate anions between the layers was determined and the preferential intercalation mechanism was discussed. These results indicate the possibility of a molecular recognition ability of LDH and it would be exploited for the chemical separation of some anions from solution.

  8. Physical properties of fixed-charge layer double hydroxides (United States)

    Hines, D. R.; Solin, S. A.; Costantino, Umberto; Nocchetti, Morena


    The physical properties of a series of layer double hydroxides (LDH) of the form [(CO3)0.195(1-x)Cl0.39x(H2O)y]:[Zn0.61Al0.39(OH)2], 0layer water molecules form a hydration ring which defines the height of the solvated, nested Cl anion. The water molecules can tilt around their C2v axis such that the height of the solvated Cl ion is a function of the number of molecules forming the hydration ring. The composition dependence of the basal spacing, determined from x-ray-diffraction powder patterns measured as a function of humidity and temperature for these materials, is a function of both the Cl concentration (x) and the number of guest layer water molecules (y). Distinct basal spacing curves are observed for fully hydrated, partially hydrated, and dehydrated materials. At x=1 the Cl end-member material exhibits a change in stacking sequence from a 3R polytype to a 2H polytype upon dehydration. The dehydrated form of this material also exhibits a (3×3)R30° superlattice ordering of the Cl ions. Due to the nesting of the Cl ion and the active nature of the water molecules, the basal spacing vs x curve for the dehydrated materials is the only curve that can be fit by the discrete finite layer rigidity model. The interlayer rigidity parameter for LDH materials has been determined to be p=4.84+/-0.06 indicating that these materials are stiffer than class-II layered solids but not as stiff as class-III layered solids.

  9. Effective Construction of High-quality Iron Oxy-hydroxides and Co-doped Iron Oxy-hydroxides Nanostructures: Towards the Promising Oxygen Evolution Reaction Application (United States)

    Zhang, Xinyu; An, Li; Yin, Jie; Xi, Pinxian; Zheng, Zhiping; Du, Yaping


    Rational design of high efficient and low cost electrocatalysts for oxygen evolution reaction (OER) plays an important role in water splitting. Herein, a general gelatin-assisted wet chemistry method is employed to fabricate well-defined iron oxy-hydroxides and transitional metal doped iron oxy-hydroxides nanomaterials, which show good catalytic performances for OER. Specifically, the Co-doped iron oxy-hydroxides (Co0.54Fe0.46OOH) show the excellent electrocatalytic performance for OER with an onset potential of 1.52 V, tafel slope of 47 mV/dec and outstanding stability. The ultrahigh oxygen evolution activity and strong durability, with superior performance in comparison to the pure iron oxy-hydroxide (FeOOH) catalysts, originate from the branch structure of Co0.54Fe0.46OOH on its surface so as to provide many active edge sites, enhanced mass/charge transport capability, easy release oxygen gas bubbles, and strong structural stability, which are advantageous for OER. Meanwhile, Co-doping in FeOOH nanostructures constitutes a desirable four-electron pathway for reversible oxygen evolution and reduction, which is potentially useful for rechargeable metal−air batteries, regenerative fuel cells, and other important clean energy devices. This work may provide a new insight into constructing the promising water oxidation catalysts for practical clean energy application. PMID:28272443

  10. Effective Construction of High-quality Iron Oxy-hydroxides and Co-doped Iron Oxy-hydroxides Nanostructures: Towards the Promising Oxygen Evolution Reaction Application. (United States)

    Zhang, Xinyu; An, Li; Yin, Jie; Xi, Pinxian; Zheng, Zhiping; Du, Yaping


    Rational design of high efficient and low cost electrocatalysts for oxygen evolution reaction (OER) plays an important role in water splitting. Herein, a general gelatin-assisted wet chemistry method is employed to fabricate well-defined iron oxy-hydroxides and transitional metal doped iron oxy-hydroxides nanomaterials, which show good catalytic performances for OER. Specifically, the Co-doped iron oxy-hydroxides (Co0.54Fe0.46OOH) show the excellent electrocatalytic performance for OER with an onset potential of 1.52 V, tafel slope of 47 mV/dec and outstanding stability. The ultrahigh oxygen evolution activity and strong durability, with superior performance in comparison to the pure iron oxy-hydroxide (FeOOH) catalysts, originate from the branch structure of Co0.54Fe0.46OOH on its surface so as to provide many active edge sites, enhanced mass/charge transport capability, easy release oxygen gas bubbles, and strong structural stability, which are advantageous for OER. Meanwhile, Co-doping in FeOOH nanostructures constitutes a desirable four-electron pathway for reversible oxygen evolution and reduction, which is potentially useful for rechargeable metal-air batteries, regenerative fuel cells, and other important clean energy devices. This work may provide a new insight into constructing the promising water oxidation catalysts for practical clean energy application.

  11. Arsenic adsorption by iron-aluminium hydroxide coated onto macroporous supports: Insights from X-ray absorption spectroscopy and comparison with granular ferric hydroxides. (United States)

    Suresh Kumar, Prashanth; Flores, Roxana Quiroga; Sjöstedt, Carin; Önnby, Linda


    This paper evaluates the arsenic adsorption characteristics of a macroporous polymer coated with coprecipitated iron-aluminium hydroxides (MHCMP). The MHCMP adsorbent-composite fits best with a pseudo-second order model for As(III) and a pseudo-first order kinetic model for As(V). The MHCMP shows a maximum adsorption capacity of 82.3 and 49.6 mg As/g adsorbent for As(III) and As(V) ions respectively, and adsorption followed the Langmuir model. Extended X-ray absorption fine structure showed that binding of As(III) ions were confirmed to take place on the iron hydroxides coated on the MHCMP, whereas for As(V) ions the binding specificity could not be attributed to one particular metal hydroxide. As(III) formed a bidentate mononuclear complex with Fe sites, whereas As(V) indicated on a bidentate binuclear complex with Al sites or monodentate with Fe sites on the adsorbent. The column experiments were run in a well water spiked with a low concentration of As(III) (100 μg/L) and a commercially available adsorbent (GEH(®)102) based on granular iron-hydroxide was used for comparison. It was found that the MHCMP was able to treat 7 times more volume of well water as compared to GEH(®)102, maintaining the threshold concentration of less than 10 μg As/L, indicating that the MHCMP is a superior adsorbent.

  12. Effect of Operating Parameters and Chemical Additives on Crystal Habit and Specific Cake Resistance of Zinc Hydroxide Precipitates

    Energy Technology Data Exchange (ETDEWEB)

    Alwin, Jennifer Louise [New Mexico State Univ., Las Cruces, NM (United States)


    The effect of process parameters and chemical additives on the specific cake resistance of zinc hydroxide precipitates was investigated. The ability of a slurry to be filtered is dependent upon the particle habit of the solid and the particle habit is influenced by certain process variables. The process variables studied include neutralization temperature, agitation type, and alkalinity source used for neutralization. Several commercially available chemical additives advertised to aid in solid/liquid separation were also examined in conjunction with hydroxide precipitation. A statistical analysis revealed that the neutralization temperature and the source of alkalinity were statistically significant in influencing the specific cake resistance of zinc hydroxide precipitates in this study. The type of agitation did not significantly effect the specific cake resistance of zinc hydroxide precipitates. The use of chemical additives in conjunction with hydroxide precipitation had a favorable effect on the filterability. The morphology of the hydroxide precipitates was analyzed using scanning electron microscopy.

  13. The Effect of Ultrafine Magnesium Hydroxide on the Tensile Properties and Flame Retardancy of Wood Plastic Composites

    Directory of Open Access Journals (Sweden)

    Zhiping Wu


    Full Text Available The effect of ultrafine magnesium hydroxide (UMH and ordinary magnesium hydroxide (OMH on the tensile properties and flame retardancy of wood plastic composites (WPC were investigated by tensile test, oxygen index tester, cone calorimeter test, and thermogravimetric analysis. The results showed that ultrafine magnesium hydroxide possesses strengthening and toughening effect of WPC. Scanning electron micrograph (SEM of fracture section of samples provided the positive evidence that the tensile properties of UMH/WPC are superior to that of WPC and OMH/WPC. The limited oxygen index (LOI and cone calorimeter test illustrated that ultrafine magnesium hydroxide has stronger flame retardancy and smoke suppression effect of WPC compared to that of ordinary magnesium hydroxide. The results of thermogravimetric analysis implied that ultrafine magnesium hydroxide can improve the char structure which plays an important role in reducing the degradation speed of the inner matrix during combustion process and increases the char residue at high temperature.

  14. Measurements of zinc oxide solubility in sodium hydroxide solution from 25 to 100 ℃%25~100℃下ZnO在NaOH溶液中溶解度测定

    Institute of Scientific and Technical Information of China (English)

    陈爱良; 徐冬; 陈星宇; 张文勇; 刘旭恒


    The solubility of zinc oxide in sodium hydroxide solution was measured in a closed polytetrafluoroethylene vessel from 25to 100 ℃.The ZnO solubility was determined by employing the method of isothermal solution saturation.The results show that only ZnO solid exists in the equilibrium state in the low concentration alkali regions,and the solubility of zinc oxide is almost invariable with temperature.With the increase of alkali concentration,equilibrium solid turns from ZnO to NaZn(OH)3 suddenly,this mutation is called invariant point.The alkali concentration of the invariant points increases with increasing temperature,but the solubility of NaZn(OH)3 decreases with increasing alkali concentration at the same temperature.At the same Na2O concentration,the higher the temperature is,the higher the solubility of NaZn(OH)3 is.%采用等温溶解饱和度法,在25~100°C下于密闭的聚四氟乙烯容器内测定ZnO在NaOH溶液中的溶解度.结果表明:在低浓度NaOH溶液中,平衡体系中只有ZnO一种固相存在,此时氧化锌的溶解度基本上不随温度改变.随着NaOH浓度增高,平衡固相由ZnO突然转变为NaZn(OH)3.这个突变点叫不变点.不变点的NaOH浓度随着温度的升高而增加,但在同一温度下NaZn(OH)3的溶解度随NaOH浓度增加而减少.在同Na2O浓度下,温度越高,NaZn(OH)3的溶解度越高.

  15. Experimental and Theoretical Studies of Pressure Broadened Alkali-Metal Atom Resonance Lines (United States)

    Shindo, F.; Zhu, C.; Kirby, K.; Babb, J. F.


    We are carrying out a joint theoretical and experimental research program to study the broadening of alkali atom resonance lines due to collisions with helium and molecular hydrogen for applications to spectroscopic studies of brown dwarfs and extrasolar giant planets.

  16. Is electronegativity a useful descriptor for the pseudo-alkali metal NH4? (United States)

    Whiteside, Alexander; Xantheas, Sotiris S; Gutowski, Maciej


    Molecular ions in the form of "pseudo-atoms" are common structural motifs in chemistry, with properties that are transferrable between different compounds. We have determined one such property--the electronegativity--for the "pseudo-alkali metal" ammonium (NH(4)), and evaluated its reliability as a descriptor versus the electronegativities of the alkali metals. The computed properties of ammonium's binary complexes with astatine and of selected borohydrides confirm the similarity of NH(4) to the alkali metal atoms, although the electronegativity of NH(4) is relatively large in comparison to its cationic radius. We have paid particular attention to the molecular properties of ammonium (angular anisotropy, geometric relaxation and reactivity), which can cause deviations from the behaviour expected of a conceptual "true alkali metal" with this electronegativity. These deviations allow for the discrimination of effects associated with the molecular nature of NH(4).

  17. The ecology and genetics of alkali bulrush (Schoenoplectus maritimus) : Management implications (United States)

    US Fish and Wildlife Service, Department of the Interior — Alkali bulrush (Schoenoplectus maritimus) is an important wetland plant species, in the Intermountain West. However, there is a lack of knowledge on how best to...

  18. Use of Fly Ash in the Mitigation of Alkali-Silica Reaction in Concrete (United States)


    crystallinity of the silica and its solubility. Common reactive minerals susceptible to ASR include strained quartz, cristobalite , opal, obsidian, chert, and...residues, whereas alkali-silica reactive components include opal, cristobalite , tridymite, siliceous and some intermediate volcanic glass, chert

  19. Studies of Alkali Sorption Kinetics for Pressurized Fluidized Bed Combustion by High Pressure Mass Spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Wolf, K.J.; Willenborg, W.; Fricke, C.; Prikhodovsky, A.; Hilpert, K.; Singheiser, L.


    This work describes the first approach to use High Pressure Mass Spectrometry (HPMS) for the quantification and analysis of alkali species in a gas stream downstream a sorbent bed of different tested alumosilicates.

  20. Fluid Composititon and Carbon & Oxygen Isotope Geochemistry of Cenozoic Alkali Basalts in Eastern China

    Institute of Scientific and Technical Information of China (English)

    张铭杰; 王先彬; 等


    The fluid compositions of Cenozoic alkali basalts in eastern China have been determined by the pyrolysis-MS method,meanwhile the carbon and oxygen isotopic compositions of CO2 released from these samples at different heating temperatures have been analyzed by the vacuum step-heating method.The data show the volatiole heterogeneity in upper-mantle sources and different evolution trends of alkali basaltic magmas in eastern China,and these alkali basaltic magmas may be generated in the oxidizing milieu,as compared with mantle-derived xenoliths in these alkali basalts,and exotic volatile components were mixed into these magmas in the process of their formation and development.

  1. Enhancement of tensile strength of lignocellulosic jute fibers by alkali-steam treatment. (United States)

    Saha, Prosenjit; Manna, Suvendu; Chowdhury, Sougata Roy; Sen, Ramkrishna; Roy, Debasis; Adhikari, Basudam


    The physico-chemical properties of jute fibers treated with alkali (NaOH) solution have been investigated in this study. The treatments were applied under ambient and elevated temperatures and high pressure steaming conditions. To the knowledge of these authors the influence of alkali-steam treatment on the uniaxial tensile strength of natural ligno-cellulosic fibers, such as jute, has not been investigated earlier. The results from this investigation indicate that a 30 min dipping of the fibers in 0.5% alkali solution followed by 30 min alkali-steam treatment leads to an increase in the tensile strength of up to 65%. The increase appears to be due to fiber separation and removal of non-cellulosic materials, which, in turn, resulted in an increased crystallinity.

  2. Improvement of a polarized alkali ion source by means of optical pumping

    Energy Technology Data Exchange (ETDEWEB)

    Dreves, W.; Koch, E.; Jaensch, H.; Kamke, W.; Broermann, W.; Fick, D.


    A source for polarized alkali ions can be improved considerably by optical pumping of the atom beam in combination with a modified weak field transition. M-level populations were investigated using laser induced fluorescence in a magnetic field.

  3. A contribution to the surface characterization of alkali metal sulfates

    Energy Technology Data Exchange (ETDEWEB)

    Fantauzzi, Marzia; Rigoldi, Americo; Elsener, Bernhard; Atzei, Davide; Rossi, Antonella, E-mail:


    Highlights: • Full electronic characterization of alkali metals sulfates by X-ray photoelectron spectroscopy and X-ray induced Auger electron spectroscopy. • Curve-fitting of SKLL signals makes possible to clarify the role of the cation in the series of alkali metal sulfates. • Differences in the binding energies and Auger parameter are discussed in terms of the electronic properties and the polarizability of the cation. • The line intensities are analyzed and a thorough quantitative analysis is presented. - Abstract: The analytical characterization of surfaces of sulfur-bearing samples that present sulfides, polysulfides and/or elemental sulfur as reaction products can be difficult by simply relying on the binding energy of the S2p X-ray photoelectron signals, due to the small chemical shifts. In such cases the Auger parameter concept can be used to distinguish among different chemical states, but this requires a model to curve fit complex Auger SKLL signals in order to resolve the contributions arising from sulfur in different chemical states on the surface. With this scope a detailed X-ray photoelectron spectroscopy (XPS) and X-ray induced Auger electron spectroscopy (XAES) surface analytical study of the group IA sulfates is presented in this paper. Sulfates were chosen as model compounds for curve fitting the X-ray induced SKLL spectra since in these compounds sulfur is present in a unique chemical state. For the first time the multicomponent SKLL spectra are fitted with model functions consisting of an intense {sup 1}D and a low intensity {sup 1}S contribution with constant energy difference of 8 eV. It was found that the kinetic energy of the SK{sub 2,3}L{sub 2,3} ({sup 1}D) line increases from 2105.1 ± 0.1 to 2107.5 ± 0.2 eV whereas the corresponding S2p{sub 3/2} binding energy decreases from 169.5 ± 0.1 eV for Li{sub 2}SO{sub 4} to 167.8 ± 0.1 eV for Cs{sub 2}SO{sub 4}. Shifts to lower binding energy values are observed also for S2p, S2s and O1

  4. Synthesis of Zn–Fe layered double hydroxides via an oxidation process and structural analysis of products

    Energy Technology Data Exchange (ETDEWEB)

    Morimoto, Kazuya, E-mail: [Institute for Geo-Resources and Environment, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Higashi, Tsukuba, Ibaraki 305-8567 (Japan); Tamura, Kenji [Environmental Remediation Materials Unit, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044 (Japan); Anraku, Sohtaro [Graduate School of Engineering, Hokkaido University, Kita 13 Nishi 8, Kita-ku, Sapporo 060-8628 (Japan); Sato, Tsutomu [Faculty of Engineering, Hokkaido University, Kita 13 Nishi 8, Kita-ku, Sapporo 060-8628 (Japan); Suzuki, Masaya [Institute for Geo-Resources and Environment, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Higashi, Tsukuba, Ibaraki 305-8567 (Japan); Yamada, Hirohisa [Environmental Remediation Materials Unit, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044 (Japan)


    The synthesis of Zn–Fe(III) layered double hydroxides was attempted, employing different pathways using either Fe(II) or Fe(III) species together with Zn as the initial reagents. The product derived from the synthesis employing Fe(II) was found to transition to a Zn–Fe(III) layered double hydroxides phase following oxidation process. In contrast, the product obtained with Fe(III) did not contain a layered double hydroxides phase, but rather consisted of simonkolleite and hydrous ferric oxide. It was determined that the valency of the Fe reagent used in the initial synthesis affected the generation of the layered double hydroxides phase. Fe(II) species have ionic radii and electronegativities similar to those of Zn, and therefore are more likely to form trioctahedral hydroxide layers with Zn species. - Graphical abstract: The synthesis of Zn–Fe(III) layered double hydroxides was attempted, employing different pathways using either Fe(II) or Fe(III) species together with Zn as the initial reagents. - Highlights: • Iron valency affected the generation of Zn–Fe layered double hydroxides. • Zn–Fe layered double hydroxides were successfully synthesized using Fe(II). • Fe(II) species were likely to form trioctahedral hydroxide layers with Zn species.

  5. "Textbook" adsorption at "nontextbook" adsorption sites: Halogen atoms on alkali halide surfaces


    Li, B.; Michaelides, A.; Scheffler, M.


    Density-functional theory (DFT) and second order Møller-Plesset perturbation theory calculations indicate that halogen atoms bond preferentially to halide substrate atoms on a series of alkali halide surfaces, rather than to the alkali atoms as might be anticipated. An analysis of the electronic structures in each system reveals that this novel adsorption mode is stabilized by the formation of textbook two-center three-electron covalent bonds. The implications of these findings to, for exampl...

  6. Cold three-body collisions in hydrogen-hydrogen-alkali atomic system

    CERN Document Server

    Wang, Yujun; Esry, B D


    We have studied hydrogen-hydrogen-alkali three-body systems in the adiabatic hyperspherical representation. For the spin-stretched case, there exists a single $X$H molecular state when $X$ is one of the bosonic alkali atoms: $^7$Li, $^{23}$Na, $^{39}$K, $^{87}$Rb and $^{133}$Cs. As a result, the {\\em only} recombination process is the one that leads to formation of $X$H molecules, H+H+$X

  7. Endoscopic pyloroplasty for severe gastric outlet obstruction due to alkali ingestion in a child


    Dehghani, Seyed Mohsen; Aldaghi, Mitra; Javaherizadeh, Hazhir


    A common belief is that alkali ingestion causes severe esophageal damage and limited gastric injury due to the buffering action of acid. Gastric injury has been observed in patients who ingested alkali. Gastric outlet obstruction (GOO) secondary to caustic ingestion occurs due to fibrosis after resolution of the acute injury and inflammation, most commonly 6 to 12 weeks after initial ingestion. The traditional treatment for GOO related to ingestion of corrosive agents is surgery. Experience w...

  8. Properties of Hydrated Alkali Metals Aimed at the Ion Channel Selectivity

    Institute of Scientific and Technical Information of China (English)

    AN Hai-Long; LIU Yu-Zhi; ZHANG Su-Hua; ZHAN Yong; ZHANG Hai-Lin


    The hydration structure properties of different alkali metal ions with eight water molecules and potassium ions with different numbers of water molecules are studied using the mixed density functional theory, B3LYP, with 6-311G basis set. The hydration structures are obtained from structure optimization and the optimum numbers of water molecules in the innermost hydration shell for the alkali metal ions are found. Some useful information about the ion channel selectivity is presented.

  9. Alkali Metal-incorporated Mesoporous Smectites:Crystallinity and Textural Properties

    Institute of Scientific and Technical Information of China (English)

    HE Yan-feng; Shinichiro Fujita; Nobuhiro Iwasa; Bhalchandra M. Bhanage; Masahiko Arai


    A series of mesoporous smectite-like materials incorporated with alkali metals such as Li, Na, K and Cs has been synthesized with the hydrothermal method. The crystalline and the pore structures of the materials synthesized significantly change with the introduction of alkali metals. The addition of Li gives highly ordered layer phases, while the incorporation of Cs yields much less crystalline structures. Although Na or K has little effect on the crystalline structure, they modify the pore structure.

  10. The Feasibility of ASP Flooding with Low Alkali Concentration in Heterogeneous Reservoirs

    Institute of Scientific and Technical Information of China (English)

    HouJirui; ZhangShufen; YangJinzong; YueXiang'an


    In this paper, as far as the ASP flooding in the pilot area of Daqing oilfield is concerned, the effect of apparent viscosity of ASP solution on enhanced oil recovery have been studied by comparison of experiments on artificial heterogeneous cores with on natural cores.The results showed that the decrease in the concentration of alkali could increase tile apparent viscosity of ASP solutions, namely, the apparent viscosity increased and the IFF couldn't get ultra low, and the oil recovery efficiency by ASP solution with a reasonably lower concentration of alkali was not less than that with a higher concentration of alkali and ultra low IFF. The experiments with models having impermeable interlayers between adjacent layers, and by means of “co-injection and separate production” showed that the ASP solution with a higher viscosity and a lower alkali concentration was more beneficial to starting-up medium and low permeability layers and enhancing total oil recovery. Therefore, to heterogeneous reservoir, as factors of affecting oil recovery, the apparent viscosity may be more important than the ultralow IFF. Furthermore, on the premise that the concentration of surfactant and the concentration of polymer keep constant, ASP flooding with low alkali concentration not only enlarges the selectable range of surfactants and decreases the cost of ASP flooding, but also solves the problem of alkali scales. Finally, a dynamic absorption experiment was performed with a 0.5 meter long linked-up natural core to determine alkali wastage in formation. The result being accord with the application case in the pilot confirmed that it was not necessary to add the alkali too much in ASP flooding from a new direction.

  11. Impact of alkali salts on the kinetics and microstructural development of cementitious systems


    Mota Gassó, Berta


    Supplementary cementitious materials (SCM) lower the environmental impact of cement and concrete but react more slowly than Portland cement, which therefore limits the levels of substitution possible as reasonable early strengths are necessary. One of the main factors affecting the reaction of the SCMs is the alkalinity of the pore solution. However, alkalis do not only affect SCMs, but also the clinker phases. It is generally accepted that alkalis accelerate the hydration of Portland cement ...

  12. Thermochemical Ablation Therapy of VX2 Tumor Using a Permeable Oil-Packed Liquid Alkali Metal



    Objective Alkali metal appears to be a promising tool in thermochemical ablation, but, it requires additional data on safety is required. The objective of this study was to explore the effectiveness of permeable oil-packed liquid alkali metal in the thermochemical ablation of tumors. Methods Permeable oil-packed sodium–potassium (NaK) was prepared using ultrasonic mixing of different ratios of metal to oil. The thermal effect of the mixture during ablation of muscle tissue ex vivo was evaluat...

  13. Calculated Pressure Induced BCC-FCC Phase Transitions in Alkali Metals


    DAĞISTANLI, Hamdi; MUTLU, R. Haluk


    The partial occupation numbers and density of states (DOS), and the total DOS at the Fermi level are calculated as a function of reduced atomic volume for bcc and fcc alkali metals employing the linear-muffin-tin-orbital (LMTO) method. By means of the abrupt changes obtained in the partial and total DOS values at the Fermi level, good agreement with regard to experiment were found in predicting the bcc-fcc transition volumes of the alkali metals.

  14. Geochronology of Ailaoshan-Jinshajiang alkali- rich intrusive rocks and their Sr and Nd isotopic characteristics

    Institute of Scientific and Technical Information of China (English)

    张玉泉; 谢应雯


    Twenty-nine isotopic ages, ranging from 41 to 27 Ma, are presented for the alkali-rich intrusive rocks and their coexisting alkaline volcanic rocks, lamprophyres and acidic porphyries, indicating that they are Tertiary in age. The alkali-rich intrusive rocks have 143Nd/144Nd ratios from 0. 512 415 to 0. 512 544, and 87Sr/86Sr ratios from 0.705 4 to 0.706 8, suggesting that their material originates from an enriched mantle source.





    Sodium and potassium combinations existing in phosphogypsum are highly soluble and remain in the filtrate, their amount increasing with each recycle. It has been determined that the amount of alkalis in the recycling filtrate depends on an amount of alkalis in uncleaned phosphogypsum, a number of recycles in the filtrate, the technology of the phosphogypsum pulp preparation and an amount of soluble phosphates. New phosphate formations composed in an acid medium (pH = 4.5-5) are well crystaliz...

  16. An optical criterion to obtain miscible mixed crystals in alkali halides



    This work gives a novel criterion to predict the formation of alkali halide solid solutions and discusses some results obtained in the development of ternary and quaternary miscible crystalline dielectric mixtures of alkali halides. These mixtures are miscible in any concentration of their components. The miscibility of these mixed crystals is quite related to the F center through the behavior observed in the spectral position of the optical absorption F band as a function of the lattice cons...

  17. The influence of alkali treatment on banana fibre’s mechanical properties

    Directory of Open Access Journals (Sweden)

    Julio César Mejía Osorio


    Full Text Available This work analyses the effect of alkali treatment on the mechanical properties of banana fibre (Musa Paradisiaca. Fibres were extracted from the pseudostem by a defibring machine; they were mercerised and modified by 5% NaOH (w/v alkali treatment. Morphological characterisation showed that treated fibres’ surface was rougher than that of untreated fibres. Mechanical characterisation indicated that Young’s modulus, ultimate tensile strength and strain became decreased by increasing both treated and untreated fibres’ diameter.

  18. Wavelength diversity in optically pumped alkali vapor lasers (United States)

    Perram, Glen P.


    Alternative wavelengths for optically pumped alkali vapor lasers have been developed using single photon excitation of higher lying P-states, stimulated Raman processes, two-photon excitation of S and D states, and electric quadruple excitation on S-D transitions. Two photon excitation of Cs 72D leads to competing and cascade lasing producing red and infrared lasers operating on the D-P transitions, followed by ultraviolet, blue, the standard near infrared DPAL transitions operating on P-S transitions. The S-D pump transitions are fully bleached at pump intensities exceeding 1 MW/cm2, allowing for lasing transitions that terminate on the ground state. The kinetics of these systems are complex due to competition for population inversion among the many optical transitions. An optically pumped mid-infrared rubidium pulsed, mirrorless laser has also been demonstrated in a heat pipe along both the 62P3/2 - 62S1/2 transition at 2.73 μm and the 62P1/2 - 62S1/2 transition at 2.79 μm with a maximum energy of 100 nJ. Performance improves dramatically as the rubidium vapor density is increased, in direct contradiction with the prior work. No scaling limitations associated with energy pooling or ionization kinetics have been observed. Practical application for infrared counter measures depends on the further development of blue diode pump sources. Finally, stimulated electronic Raman scattering and hyper-Raman processes in potassium vapor near the D1 and D2 lines have been observed using a stable resonator and pulsed laser excitation. First and second order Stokes and anti-Stokes lines were observed simultaneously and independently for a pump laser tuning range exceeding 70 cm-1. When the pump is tuned between the K D1 and D2 lines, an efficient hyper-Raman process dominates with a slope efficiency that exceeds 10%. Raman shifted laser may be useful as a target illuminator or atmospheric compensation beacon for a high power diode pumped alkali laser.

  19. Mistletoe alkali inhibits peroxidation in rat liver and kidney

    Institute of Scientific and Technical Information of China (English)

    Zheng-Ming Shi; Ping Feng; Dong-Qiao Jiang; Xue-Jiang Wang


    AIM: To explore the antioxidant and free radical scavenger properties of mistletoe alkali (MA).METHODS: The antioxidant effect of mistletoe alkali on the oxidative stress induced by carbon tetrachloride (CCl4) in rats was investigated. The rats were divided into four groups (n = 8): CCl4-treated group (1 mL/kg body weight), MA -treated group (90 mg/kg), CCl4+MA-treated group and normal control group. After 4 wk of treatment,the level of malondialdehyde (MDA), a lipid peroxidation product (LPO) was measured in serum and homogenates of liver and kidney. Also, the level of glutathione (GSH),and activities of glutathione reductase (GR), glutathione peroxidase (GSPx), superoxide dismutase (SOD), and glutathione-S-transferase (GST) in liver and kidney were determined. Scavenging effects on hydroxyl free radicals produced in vitro by Fenton reaction were studied by ESR methods using 5,5-dimethyl-1-pyrroline-N-oxidesource. Urinary 8-hydroxydeoxyguanosine (8-OHdG) was determined by competitive ELISA.RESULTS: In CCl4-treated group, the level of LPO in serum of liver and kidney was significantly increased compared to controls. The levels of GSH and enzyme activities of SOD, GSPx and GR in liver and kidney were significantly decreased in comparison with controls. In CCl4+MA-treated group, the changes in the levels of LPO in serum of liver and kidney were not statistically significant compared to controls. The levels of SOD, GSPx and GR in liver and kidney were significantly increased in comparison with controls. There was a significant difference in urinary excretion of 8-OHdG between the CCl4-treated and MA-treated groups.CONCLUSION: Oxidative stress may be a major mechanism for the toxicity of CCl4. MA has a protective www.wjgnet.comeffect against CCl4 toxicity by inhibiting the oxidative damage and stimulating GST activities. Thus, clinical application of MA should be considered in cases with carbon tetrachloride-induced injury.

  20. Zintl cluster chemistry in the alkali-metal-gallium systems

    Energy Technology Data Exchange (ETDEWEB)

    Henning, Robert [Iowa State Univ., Ames, IA (United States)


    Previous research into the alkali-metal-gallium systems has revealed a large variety of networked gallium deltahedra. The clusters are analogues to borane clusters and follow the same electronic requirements of 2n+2 skeletal electrons for closo-deltahedra. This work has focused on compounds that do not follow the typical electron counting rules. The first isolated gallium cluster was found in Cs8Ga11. The geometry of the Ga117- unit is not deltahedral but can be described as a penta-capped trigonal prism. The reduction of the charge from a closo-Ga1113- to Ga117- is believed to be the driving force of the distortion. The compound is paramagnetic because of an extra electron but incorporation of a halide atom into the structure captures the unpaired electron and forms a diamagnetic compound. A second isolated cluster has been found in Na10Ga10Ni where the tetra-capped trigonal prismatic gallium is centered by nickel. Stabilization of the cluster occurs through Ni-Ga bonding. A simple two-dimensional network occurs in the binary K2Ga3 Octahedra are connected through four waist atoms to form a layered structure with the potassium atoms sitting between the layers. Na30.5Ga60-xAgx is nonstoichiometric and needs only a small amount of silver to form (x ~ 2-6). The structure is composed of three different clusters which are interconnected to form a three-dimensional structure. The RbGa3-xAux system is also nonstoichiometric with a three-dimensional structure composed of Ga8 dodecahedra and four-bonded gallium atoms. Unlike Na30.5Ga60-xAgx, the RbGa3 binary is also stable. The binary is formally a Zintl phase but the ternary is not. Some chemistry in the alkali-metal-indium system also has been explored. A new potassium-indium binary

  1. Mixing Acid Salts and Layered Double Hydroxides in Nanoscale under Solid Condition

    Directory of Open Access Journals (Sweden)

    Hirokazu Nakayama


    Full Text Available The immobilization of potassium sorbate, potassium aspartate and sorbic acid in layered double hydroxide under solid condition was examined. By simply mixing two solids, immobilization of sorbate and aspartate in the interlayer space of nitrate-type layered double hydroxide, so called intercalation reaction, was achieved, and the uptakes, that is, the amount of immobilized salts and the interlayer distances of intercalation compounds were almost the same as those obtained in aqueous solution. However, no intercalation was achieved for sorbic acid. Although intercalation of sorbate and aspartate into chloride-type layered double hydroxide was possible, the uptakes for these intercalation compounds were lower than those obtained using nitrate-type layered double hydroxide. The intercalation under solid condition could be achieved to the same extent as for ion-exchange reaction in aqueous solution, and the reactivity was similar to that observed in aqueous solution. This method will enable the encapsulation of acidic drug in layered double hydroxide as nano level simply by mixing both solids.

  2. Vibrational dynamics of aqueous hydroxide solutions probed using broadband 2DIR spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Mandal, Aritra [Department of Chemistry, James Franck Institute, and Institute for Biophysical Dynamics, University of Chicago, Chicago, Illinois 60637 (United States); Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 (United States); Tokmakoff, Andrei, E-mail: [Department of Chemistry, James Franck Institute, and Institute for Biophysical Dynamics, University of Chicago, Chicago, Illinois 60637 (United States)


    We employed ultrafast transient absorption and broadband 2DIR spectroscopy to study the vibrational dynamics of aqueous hydroxide solutions by exciting the O–H stretch vibrations of the strongly hydrogen-bonded hydroxide solvation shell water and probing the continuum absorption of the solvated ion between 1500 and 3800 cm{sup −1}. We observe rapid vibrational relaxation processes on 150–250 fs time scales across the entire probed spectral region as well as slower vibrational dynamics on 1–2 ps time scales. Furthermore, the O–H stretch excitation loses its frequency memory in 180 fs, and vibrational energy exchange between bulk-like water vibrations and hydroxide-associated water vibrations occurs in ∼200 fs. The fast dynamics in this system originate in strong nonlinear coupling between intra- and intermolecular vibrations and are explained in terms of non-adiabatic vibrational relaxation. These measurements indicate that the vibrational dynamics of the aqueous hydroxide complex are faster than the time scales reported for long-range transport of protons in aqueous hydroxide solutions.

  3. Zimmer slipstream magnesium hydroxide recovery demonstration. Volume II of II. Appendices

    Energy Technology Data Exchange (ETDEWEB)



    Dravo Lime has for many years supplied magnesium containing lime in the ranges of 3-6% MgO. Several years ago Dravo Lime realized the potential operating savings its FGD customers could benefit from if magnesium could be recovered from FGD waste streams. As a result, several different proprietary processes have been developed for the recovery of magnesium hydroxide. These recovery processes include steps for magnesium hydroxide separation, purification, and crystal growth. The process implemented at The Cincinnati Gas Electric Company`s Wm. H. Zimmer Station was piloted by Dravo Lime Company at Allegheny Power System`s Mitchell Station near Monongahela, PA during the fourth quarter in 1989 and first quarter in 1990. This pilot work was the foundation for further development of the ThioClear process at Dravo`s pilot plant at CG&E Miami Fort Station. The ThioClear process is a closed loop version of the magnesium hydroxide recovery process with the same unit operations and products but also including an absorber tower for scrubbing flue gas. Testing at Miami Fort of the ThioClear process led to improvements in separation of magnesium hydroxide from gypsum that are part of the magnesium hydroxide recovery process installed at Zimmer Station. This document contains the Appendices for this report.

  4. The Effect of Calcium Hydroxide As an Intracanal Medication of The Apical Microleakage

    Directory of Open Access Journals (Sweden)

    Heshmat Mohajer AR


    Full Text Available Background and Aims: Nowadays, calcium hydroxide is used as a dressing for canal sterilization and repair progression of apical lesions. The aim of this study was to investigate the effect of calcium hydroxide as an intracanal medicament on the apical microleakage of root filling.Materials and Methods: In this experimental study, 46 extracted single-rooted human teeth were instrumented with step-back technique to master apical file (MAF size 35. Specimens were randomly divided into 2 groups (n = 20. In group 1, the specimens were treated with calcium hydroxide intracanal medication; and in group 2, the samples did not receive any medication. The teeth were incubated in 100% humidity at 37°C for one week. After that, calcium hydroxide was removed using irrigation with normal saline and reaming with MAF. The root canals were obturated with gutta- percha and AH26 sealer using lateral compaction technique. Specimens were incubated in 100% humility at 37°C for 72 hours and then immersed in India ink for 1 week. Finally, the teeth were cleared and the maximum linear dye penetration was measured under a stereomicroscope at 4X magnification. The data were analyzed by T-test and Chi-square.Results: There was no significant difference between the two experimental groups (P=0.068. Conclusion: The findings of this study indicated that using calcium hydroxide as an intracanal medicament did not influence the apical microleakage after final obturation of the root canal system.

  5. Relationship between sealing ability of Activ GP and Gutta Flow and methods of calcium hydroxide removal

    Directory of Open Access Journals (Sweden)

    Vineeta Nikhil


    Full Text Available Aim: To evaluate the effect of method of calcium hydroxide intracanal dressing removal, on sealing ability of Gutta Flow and Activ GP. Materials and Methods: Seventy extracted mandibular premolars were sectioned at CEJ and canals were prepared with profile 4% rotary file till #40. Canals were filled with calcium hydroxide, coronally sealed with Cavit G and stored at 37°C. After 7 days, samples were divided on the basis of calcium hydroxide removal method (Master apical file, Navi Tip FX, and F File and obturating material (Activ GP and Gutta Flow. Three coats of nail polish were applied except 2 mm around apical foramen and samples were immersed in India ink dye, sectioned, and observed under stereomicroscope for microleakage. Results: The results were statistically analyzed with one way ANOVA-F with Tukey HSD test with the null hypothesis set as 5%. Conclusions: The seal of the canal system was adversely impacted by residual calcium hydroxide when Activ GP and Gutta Flow were used as obturating material and the sealing ability of Activ GP and Gutta Flow was better when MAF was used for removal of calcium hydroxide than F file or Navi tip FX.

  6. Chlorine behavior during co-hydrothermal treatment of high alkali coal and PVC (United States)

    Huang, N.; Zhao, P. T.; Li, Z. Z.; Li, T.


    The hydrothermal treatment (HT) is an effective method to remove chlorine from chlorinated wastes under mild conditions. However, the alkali was required to improve the dechlorination efficiency. Meanwhile, the alkalis contents removed was necessary to realize the clean and highly efficient utilization of coal. This work was trying to investigate the feasibility of simultaneously removal alkalis and chlorine by co-hydrothermal treatment of PVC and high-alkali coal. The effect of operating conditions including the HT temperature, the holding time and particle sizes of coal on the dechlorination efficiency (DE) of PVC during the HT process was experimentally studied in this work. The results show that the DE increased with the rise of: 1) particle sizes (0.054~0.22mm), 2) holding time (30~90 min) and 3) temperature (240~300 °C). In detail, under 300 °C and 60min of holding time, the 85.18% of DE with first PS was lower than the 93.93% of DE with second PS and 100% of DE with third PS. The organic chlorine mainly transferred into chloridion in aqueous solution in HT process. All the results indicate that it is a prospective way to simultaneously removal alkalis and chlorine by co-hydrothermal treatment of chlorinated wastes and high-alkali coal.

  7. Promoting Effect of Inorganic Alkali on Carbon Dioxide Adsorption in Amine-Modified MCM-41

    Directory of Open Access Journals (Sweden)

    Yang Teng


    Full Text Available Three kinds of inorganic alkali are introduced into tetraethylenepentamine (TEPA and polyethyleneimine (PEI-modified MCM-41 as the CO2 adsorbents. X-ray diffraction, N2 adsorption, fourier-transform infrared and thermo gravimetric analysis are used to characterize the surface structures and the thermal stability of adsorbents. Chemical titration method is used to measure the alkali amounts of adsorbents. Thermo-gravimetric analysis with 10% CO2/90% N2 as the simulated flue gas is used to test the CO2 adsorption performance of adsorbents. The results show that all three kinds of inorganic alkali-containing adsorbents exhibit higher CO2 adsorption capability than traditional TEPA and PEI modified samples. Ca(OH2 and PEI modified samples exhibit the highest adsorption capacity and recyclable property. The introduction of inorganic alkali changes the chemical adsorption mechanism between CO2 and adsorbent surface due to the increased hydroxyl groups. The CO2 adsorption capacities have a linear dependence relation with the alkali amounts of adsorbents, indicating that alkali amount is a critical factor for the exploration of novel adsorbents.

  8. Alkali production in the mouth and its relationship with certain patient's characteristics

    Directory of Open Access Journals (Sweden)

    Valeria Veiga GORDAN


    Full Text Available Objectives To assess the relationships among alkali production, diet, oral health behaviors, and oral hygiene. Methods Data from 52 subjects including demographics, diet, and oral hygiene scores were analyzed against the level of arginine and urea enzymes in plaque and saliva samples. An oral habit survey was completed that included: use of tobacco (TB, alcohol (AH, sugary drinks (SD, and diet. Alkali production through arginine deiminase (ADS and urease activities were measured in smooth-surface supragingival dental plaque and un stimulated saliva samples from all subjects. ADS and urease activities were measured by quantification of the ammonia generated from the incubation of plaque or saliva samples. Spearman correlations were used to compute all associations. Results Participants in the lowest SES (Socio-economic status group had the habit of consuming sugary drinks the most and had the highest rate of tobacco use. Males consumed significantly more alcohol than females. No significant relationship was found between age or gender and alkali production. Higher rates of sugary drink consumption and tobacco use were significantly related to lower alkali production. Conclusion The study showed a relationship between alkali production and oral hygiene, diet, and certain oral health behaviors. Poor oral hygiene was significantly associated with age, lower SES, tobacco use, and alcohol, and sugary drinks consumption. Clinical relevance Certain oral health behaviors have an impact on oral hygiene and on alkali production; it is important to address these factors with patients as a strategy for caries control.

  9. Design strategies for development of SCR catalyst: improvement of alkali poisoning resistance and novel regeneration method. (United States)

    Peng, Yue; Li, Junhua; Shi, Wenbo; Xu, Jiayu; Hao, Jiming


    Based on the ideas of the additives modification and regeneration method update, two different strategies were designed to deal with the traditional SCR catalyst poisoned by alkali metals. First, ceria doping on the V(2)O(5)-WO(3)/TiO(2) catalyst could promote the SCR performance even reducing the V loading, which resulted in the enhancement of the catalyst's alkali poisoning resistance. Then, a novel method, electrophoresis treatment, was employed to regenerate the alkali poisoned V(2)O(5)-WO(3)/TiO(2) catalyst. This novel technique could dramatically enhance the SCR activities of the alkali poisoned catalysts by removing approximately 95% K or Na ions from the catalyst and showed less hazardous to the environment. Finally, the deactivation mechanisms by the alkali metals were extensively studied by employing both the experimental and DFT theoretical approaches. Alkali atom mainly influences the active site V species rather than W oxides. The decrease of catalyst surface acidity might directly reduce the catalytic activity, while the reducibility of catalysts could be another important factor.


    Directory of Open Access Journals (Sweden)



    Full Text Available Sodium and potassium combinations existing in phosphogypsum are highly soluble and remain in the filtrate, their amount increasing with each recycle. It has been determined that the amount of alkalis in the recycling filtrate depends on an amount of alkalis in uncleaned phosphogypsum, a number of recycles in the filtrate, the technology of the phosphogypsum pulp preparation and an amount of soluble phosphates. New phosphate formations composed in an acid medium (pH = 4.5-5 are well crystalized crystals. They do not alter the filtrability of the phosphogypsum pulp. The new combinations formed in an alkaline medium (pH = 7-11 are colloidal. They settle down on the surface of the hard particles and make the filtration of the phosphogypsum pulp complicated. The filtrated phosphogypsum is more humid which causes the growth of the amount of alkalis carried out together with moisture and thus the lower alkali concentration is observed in the recycling filtrate. In the discussed case, the larger amount of soluble phosphates of uncleaned phosphogypsum is formed the larger amount of the colloidal particles in the neutralized phosphogypsum pulp which results in complicated filtration. In all the cases, the alkali concentration in the recycling filtrate approaches the maximum degree which would take place if alkalis existing in uncleaned phosphogypsum were thawed in humidity of cleaned phosphogypsum.

  11. pH dependency of hydrogen fermentation from alkali-pretreated sludge

    Institute of Scientific and Technical Information of China (English)


    Batch tests were carried out to study the possibility of hydrogen production from alkali-pre- treated sludge without seed and the pH dependency of hydrogen fermentation from alkali-pretreated sludge. Experimental results showed that the sewage sludge with alkali-pretreatment could be successfully applied to biologically producing hydrogen without seed and extra-feed. The results also showed that the initial pH value of sewage sludge was an important factor throughout the hydrogen fermentation of alkali-pretreated sludge. The maximum hydrogen yield was obtained at initial pH value of 11.0 (14.4 mL·g VS-1). The hydrogen yield of alkali-pretreated sludge at alkaline initial pH value was much higher than that of acidic or neutral initial pH value. The optimal pH value of hydrogen production from alkali- pretreated sludge was approximately 9.5. The consumption of hydrogen could be inhibited when the pH value of sludge was above 8.5. The change of hydrogen yield at various initial pH values was similar to that of sludge SCOD. The change of sludge pH value was slow and acetate was the major component of volatile fatty acids produced in the process of hydrogen production. The yield and the constitution of volatile fatty acids were sensitive to the initial pH value.

  12. Alkalis in Coal and Coal Cleaning Products / Alkalia W Węglu I Productach Jego Wzbogacania (United States)

    Bytnar, Krzysztof; Burmistrz, Piotr


    In the coking process, the prevailing part of the alkalis contained in the coal charge goes to coke. The content of alkalis in coal (and also in coke) is determined mainly by the content of two elements: sodium and potasium. The presence of these elements in coal is connected with their occurrence in the mineral matter and moisture of coal. In the mineral matter and moisture of the coals used for the coke production determinable the content of sodium is 26.6 up to 62. per cent, whereas that of potassium is 37.1 up to 73.4 per cent of the total content of alkalis. Major carriers of alkalis are clay minerals. Occasionally alkalis are found in micas and feldspars. The fraction of alkalis contained in the moisture of the coal used for the production of coke in the total amount of alkalis contained there is 17.8 up to 62.0 per cent. The presence of sodium and potassium in the coal moisture is strictly connected with the presence of the chloride ions. The analysis of the water drained during process of the water-extracting from the flotoconcentrate showed that the Na to K mass ratio in the coal moisture is 20:1. Increased amount of the alkalis in the coal blends results in increased content of the alkalis in coke. This leads to the increase of the reactivity (CRI index), and to the decrease of strength (CSR index) determined with the Nippon Steel Co. method. W procesie koksowania przeważająca część zawartych we wsadzie węglowym alkaliów przechodzi do koksu. Zawartość alkaliów w węglu, a co za tym idzie i w koksie determinowana jest głównie zawartością dwóch pierwiastków: sodu i potasu. Obecność tych pierwiastków w węglu wiąże się z występowaniem ich w substancji mineralnej i wilgoci węgla. W substancji mineralnej oraz wilgoci węgli stosowanych do produkcji koksu, oznaczona zawartość sodu wynosi od 26.6 do 62.9%, a zawartość potasu od 37.1 do 73.4% alkaliów ogółem. Głównymi nośnikami alkaliów w substancji mineralnej są minera

  13. Alternative concrete based on alkali-activated slag

    Directory of Open Access Journals (Sweden)

    Puertas, F.


    Full Text Available This article reports the results of related to on the performance of concrete made with waterglass (Na2SiO3•nH2O + NaOH-activated Colombian granulated blast furnace slag. The mechanical strength and durability properties this alkali-activated slag concrete (AAS were compared to the properties of ordinary Portland cement concrete (OPC with the same proportion of binder, which ranged from 340 to 512 kg per m3 of concrete. The results indicated that increasing the proportion of slag led to improvements in the properties studied.El propósito de este artículo es dar a conocer los resultados de la evaluación del comportamiento de mezclas de hormigón producidas a partir de la activación con waterglass (Na2SiO3•nH2O + NaOH de una escoria siderúrgica granulada de alto horno colombiana. Las propiedades mecánicas y de durabilidad de los hormigones activados alcalinamente (AAS se comparan con las correspondientes mezclas de hormigón de cemento Portland (OPC producidas con igual proporción de ligante. Estas proporciones variaron entre 340 y 512 kg por m3 de hormigón. Los resultados obtenidos indican que incrementos en la proporción de la escoria contribuye a la mejora de las propiedades evaluadas.

  14. Investigating the Intercalation Chemistry of Alkali Ions in Fluoride Perovskites

    Energy Technology Data Exchange (ETDEWEB)

    Yi, Tanghong; Chen, Wei; Cheng, Lei; Bayliss, Ryan D.; Lin, Feng; Plews, Michael R.; Nordlund, Dennis; Doeff, Marca M.; Persson, Kristin A.; Cabana, Jordi


    Reversible intercalation reactions provide the basis for modern battery electrodes. Despite decades of exploration of electrode materials, the potential for materials in the nonoxide chemical space with regards to intercalation chemistry is vast and rather untested. Transition metal fluorides stand out as an obvious target. To this end, we report herein a new family of iron fluoride-based perovskite cathode materials AxK1–xFeF3 (A = Li, Na). By starting with KFeF3, approximately 75% of K+ ions were subsequently replaced by Li+ and Na+ through electrochemical means. X-ray diffraction and Fe X-ray absorption spectroscopy confirmed the existence of intercalation of alkali metal ions in the perovskite structure, which is associated with the Fe2+/3+ redox couple. A computational study by density functional theory showed agreement with the structural and electrochemical data obtained experimentally, which suggested the possibility of fluoride-based materials as potential intercalation electrodes. This study increases our understanding of the intercalation chemistry of ternary fluorides, which could inform efforts toward the exploration of new electrode materials.

  15. Improved hydrogen desorption from lithium hydrazide by alkali metal hydride

    Energy Technology Data Exchange (ETDEWEB)

    Zeng, Liang, E-mail: [Institute for Advanced Materials Research, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima 739-8530 (Japan); Miyaoka, Hiroki [Institute for Sustainable Sciences and Development, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima 739-8530 (Japan); Ichikawa, Takayuki; Kojima, Yoshitsugu [Institute for Advanced Materials Research, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima 739-8530 (Japan)


    Highlights: •LiH can dramatically improve the hydrogen desorption properties of LiNHNH{sub 2}. •KH doping had positive effect in promoting the hydrogen desorption properties of LiNHNH{sub 2}–LiH mixture. •The reaction mechanism between LiNHNH{sub 2} and LiH was studied and discussed. -- Abstract: Lithium hydrazide (LiNHNH{sub 2}), which is a white solid with 8.0 mass% of theoretical hydrogen content, was synthesized from a reaction between anhydrous hydrazine and n-butyllithium in diethyl ether. The thermodynamic properties of this compound and its detailed decomposition pathways had been investigated in our previous work. However, a number of undesired gaseous products such as hydrazine (N{sub 2}H{sub 4}) and ammonia (NH{sub 3}) were generated during the thermal decomposition of LiNHNH{sub 2}. In this work, alkali metal hydride was used to suppress the impurities in the desorbed hydrogen and improved the hydrogen desorption properties. The reaction mechanism between LiNHNH{sub 2} and LiH was also studied and discussed in this paper.

  16. Barium oxide, calcium oxide, magnesia, and alkali oxide free glass (United States)

    Lu, Peizhen Kathy; Mahapatra, Manoj Kumar


    A glass composition consisting essentially of about 10-45 mole percent of SrO; about 35-75 mole percent SiO.sub.2; one or more compounds from the group of compounds consisting of La.sub.2O.sub.3, Al.sub.2O.sub.3, B.sub.2O.sub.3, and Ni; the La.sub.2O.sub.3 less than about 20 mole percent; the Al.sub.2O.sub.3 less than about 25 mole percent; the B.sub.2O.sub.3 less than about 15 mole percent; and the Ni less than about 5 mole percent. Preferably, the glass is substantially free of barium oxide, calcium oxide, magnesia, and alkali oxide. Preferably, the glass is used as a seal in a solid oxide fuel/electrolyzer cell (SOFC) stack. The SOFC stack comprises a plurality of SOFCs connected by one or more interconnect and manifold materials and sealed by the glass. Preferably, each SOFC comprises an anode, a cathode, and a solid electrolyte.

  17. A Survey of Alkali Line Absorption in Exoplanetary Atmospheres

    CERN Document Server

    Jensen, Adam G; Endl, Michael; Cochran, William D; Koesterke, Lars; Barman, Travis S


    We obtained over 90 hours of spectroscopic observations of four exoplanetary systems with the Hobby-Eberly Telescope (HET). Observations were taken in transit and out of transit, and we analyzed the differenced spectra---i.e., the transmission spectra---to inspect it for absorption at the wavelengths of the neutral sodium (\\ion{Na}{1}) doublet at $\\lambda\\lambda5889, 5895$ and neutral potassium (\\ion{K}{1}) at $\\lambda7698$. We used the transmission spectrum at \\ion{Ca}{1} $\\lambda6122$---which shows strong stellar absorption but is not an alkali metal resonance line that we expect to show significant absorption in these atmospheres---as a control line to examine our measurements for systematic errors. We use an empirical Monte Carlo method to quantity these systematic errors. In a reanalysis of the same dataset using a reduction and analysis pipeline that was derived independently, we confirm the previously seen \\ion{Na}{1} absorption in HD 189733b at a level of $(-5.26\\pm1.69)\\times10^{-4}$ (the average val...

  18. Collisional broadening of alkali doublets by helium perturbers

    CERN Document Server

    Mullamphy, D F T; Peach, G; Venturi, V; Whittingham, I B


    We report results for the Lorentzian profiles of the Li I, Na I and K I doublets and the Na I subordinate doublet broadened by helium perturbers for temperatures up to 3000 K They have been obtained from a fully quantum-mechanical close-coupling description of the colliding atoms, the Baranger theory of line shapes and new ab initio potentials for the alkali-helium interaction. For all lines except the 769.9 nm K I line, the temperature dependence of the widths over the range 70 < T < 3000 K is accurately represented by the power law form w=aT^b with 0.37 < b < 0.43. The 769.9 K I line has this form for 500 < T < 3000 K with b = 0.49. Although the shifts have a more complex temperature dependence, they all have the general feature of increasing with temperature above T=500 K apart from the 769.9 K I line whose shift decreases with temperature.

  19. Structural properties of low-density liquid alkali metals

    Indian Academy of Sciences (India)

    A Akande; G A Adebayo; O Akinlade


    The static structure factors of liquid alkali metals have been modelled at temperatures close to their melting points and a few higher temperatures using the reverse Monte Carlo (RMC) method. The positions of 5000 atoms in a box, with full periodicity, were altered until the experimental diffraction data of the structure factor agrees with the associated model structure factor within the errors. The model generated is then analysed. The position of the first peak of the pair distribution function () does not show any significant temperature dependence and the mean bond lengths can be approximated within an interval of 3.6–5.3 Å, 4.5–6.6 Å, 4.8–6.7 Å and 5.1–7.3 Å for Na, K, Rb and Cs respectively. The cosine bond distributions show similar trend with the flattening up of the first peak with increase in temperature. In addition, the coordination numbers of these liquid metals are high due to the presence of non-covalent bonding between them. On the average, we surmise that the coordination number decreases with increase in temperature.

  20. Effect of alkali treated jute fibres on composite properties

    Indian Academy of Sciences (India)

    Dipa Ray; B K Sarkar; A K Rana; N R Bose


    Jute fibres were subjected to a 5% alkali (NaOH) solution treatment for 0, 2, 4, 6 and 8 h at 30°C. An improvement in the crystallinity in the jute fibres increased its modulus by 12%, 68% and 79% after 4, 6 and 8 h of treatment respectively. The tenacity of the fibres improved by 46% after 6 and 8 h treatment and the % breaking strain was reduced by 23% after 8 h treatment. For the 35% composites with 4 h treated fibres, the flexural strength improved from 199.1 MPa to 238.9 MPa by 20%, modulus improved from 11.89 GPa to 14.69 GPa by 23% and laminar shear strength increased from 0.238 MPa to 0.2834 MPa by 19%. On plotting the different values of slopes obtained from the rates of improvement of the flexural strength and modulus, against the NaOH treatment time, two different failure modes were apparent before and after 4 h of treatment. In the first region between 0 and 4 h, fibre pull out was predominant whereas in the second region between 6 and 8 h, transverse fracture occurred with a minimum fibre pull out. This observation was well supported by the SEM investigations of the fracture surfaces.

  1. Alkali-crown ether complexes at metal surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Thontasen, Nicha; Deng, Zhitao; Rauschenbach, Stephan [Max Planck Institute for Solid State Research, Stuttgart (Germany); Levita, Giacomo [University of Trieste, Trieste (Italy); Malinowski, Nikola [Max Planck Institute for Solid State Research, Stuttgart (Germany); Bulgarian Academy of Sciences, Sofia (Bulgaria); Kern, Klaus [Max Planck Institute for Solid State Research, Stuttgart (Germany); EPFL, Lausanne (Switzerland)


    Crown ethers are polycyclic ethers which, in solution, selectively bind cations depending on the size of the ring cavity. The study of a single host-guest complex is highly desirable in order to reveal the characteristics of these specific interactions at the atomic scale. Such detailed investigation is possible at the surface where high resolution imaging tools like scanning tunneling microscopy (STM) can be applied. Here, electrospray ion beam deposition (ES-IBD) is employed for the deposition of Dibenzo-24-crown-8 (DB24C8)-H{sup +}, -Na{sup +} and -Cs{sup +} complexes on a solid surface in ultrahigh vacuum (UHV). Where other deposition techniques have not been successful, this deposition technique combines the advantages of solution based preparation of the complex ions with a highly clean and controlled deposition in UHV. Single molecular structures and the cation-binding of DB24C8 at the surface are studied in situ by STM and MALDI-MS (matrix assisted laser desorption ionization mass spectrometry). The internal structure of the complex, i.e. ring and cavity, is observable only when alkali cations are incorporated. The BD24C8-H{sup +} complex in contrast appears as a compact feature. This result is in good agreement with theoretical models based on density functional theory calculations.

  2. The structure of alkali silicate gel by total scattering methods

    KAUST Repository

    Benmore, C.J.


    The structure of the alkali silicate gel (ASR) collected from the galleries of Furnas Dam in Brazil was determined by a pair distribution function (PDF) analysis of high energy X-ray diffraction data. Since this method is relatively new to concrete structure analysis a detailed introduction on the PDF method is given for glassy SiO2. The bulk amorphous structure of the dam material is confirmed as no Bragg peaks are observed in the scattered intensity. The real space results show that the local structure of the amorphous material is similar to kanemite (KHSi2O5:3H2O) however the long range layer structure of the crystal is broken up in the amorphous state, so that ordering only persists of the length scale of a few polyhedra. The silicate layer structure is a much more disordered than predicted by molecular dynamics models. The X-ray results are consistent with the molecular dynamics model of Kirkpatrick et al. (2005) [1] which predicts that most of the water resides in pores within the amorphous network rather than in layers. The total scattering data provide a rigorous basis against which other models may also be tested. © 2010.

  3. Electrochemistry of ytterbium (III) in molten alkali metal chlorides

    Energy Technology Data Exchange (ETDEWEB)

    Smolenski, V.; Novoselova, A. [Institute of High-Temperature Electrochemistry, Ural Division, Russian Academy of Science, Ekaterinburg, 620219 (Russian Federation); Osipenko, A. [Research Institute of Atomic Reactors, Dimitrovgrad-10, Ulyanovsk Region, 433010 (Russian Federation); Caravaca, C. [High Level Waste Unit, Nuclear Fission Division, CIEMAT, Madrid, 28040 (Spain); Cordoba, G. de [High Level Waste Unit, Nuclear Fission Division, CIEMAT, Madrid, 28040 (Spain)], E-mail:


    This work presents the electrochemical study of Yb(III) ions in molten alkali metal chlorides in the temperature range 723-1073 K. Transient electrochemical techniques such as linear sweep, cyclic and square wave voltammetry, and potentiometry at zero current have been used to investigate the reduction mechanism, transport parameters and thermodynamic properties of the reaction YbCl{sub 2} + 1/2Cl{sub 2} = YbCl{sub 3} The results obtained show that the reduction reaction Yb(III) + e{sup -} {r_reversible} Yb(II) is reversible being controlled by the rate of the mass transfer. The diffusion coefficient of [YbCl{sub 6}]{sup 3-} complex ions has been determined at different temperatures in the fused eutectic LiCl-KCl, the equimolar NaCl-KCl and the CsCl media. The apparent standard potential of the soluble-soluble redox system Yb(III)/Yb(II) has been obtained by cyclic voltammetry. The influence of the nature of the solvent on the electrochemical and thermodynamic properties of ytterbium compounds is discussed.

  4. Modelling Alkali Line Absorption and Molecular Bands in Cool DAZs

    CERN Document Server

    Homeier, D; Allard, F; Hauschildt, P H; Schweitzer, A; Stancil, P C; Weck, P F; Homeier, Derek; Allard, Nicole F.; Allard, France; Hauschildt, Peter H.; Schweitzer, Andreas; Stancil, Phillip C.; Weck, Philippe F.


    Two peculiar stars showing an apparent extremely broadened and strong NaI D absorption have been discovered in surveys for cool white dwarfs by Oppenheimer et al. (2001) and Harris et al. (SDSS, 2003). We discuss the nature of these objects using PHOENIX atmosphere models for metal-poor brown dwarfs/very low mass stars, and new white dwarf LTE and NLTE models for hydrogen- and helium-dominated atmospheres with metals. These include complete molecular formation in chemical equilibrium and a model for the alkali resonance line broadening based on the damping profiles of Allard et al. (2003), as well as new molecular line opacities for metal hydrides. First results of our calculations indicate good agreement with a hydrogen-dominated WD atmosphere with a Na abundance roughly consistent with a state of high accretion. We analyse deviations of the abundances of Na, K, Mg and Ca from the cosmic pattern and comment on implications of these results for standard accretion scenarios.

  5. Hydride encapsulation by molecular alkali-metal clusters. (United States)

    Haywood, Joanna; Wheatley, Andrew E H


    The sequential treatment of group 12 and 13 Lewis acids with alkali-metal organometallics is well established to yield so-called ''ate' complexes, whereby the Lewis-acid metal undergoes nucleophilic attack to give an anion, at least one group 1 metal acting to counter this charge. However, an alternative, less well recognised, reaction pathway involves the Lewis acid abstracting hydride from the organolithium reagent via a beta-elimination mechanism. It has recently been shown that in the presence of N,N'-bidentate ligands this chemistry can be harnessed to yield a new type of molecular main-group metal cluster in which the abstracted LiH is effectively trapped, with the hydride ion occupying an interstitial site in the cluster core. Discussion focuses on the development of this field, detailing advances in our understanding of the roles of Lewis acid, organolithium, and amine substrates in the syntheses of these compounds. Structure-types are discussed, as are efforts to manipulate cluster geometry and composition as well as hydride-coordination. Embryonic mechanistic studies are reported, as well as attempts to generate hydride-encapsulation clusters under catalytic control.

  6. Effect of Steel Fiber on Alkali activated Fly Ash Concrete

    Directory of Open Access Journals (Sweden)



    Full Text Available Concrete is the world’s most important Construction material so the demand of cement is increases. The production of cement is highly energy intensive & the production on one ton of cement liberates about one ton of CO2 to atmosphere. The contribution of cement industry to the greenhouse gas emission is estimated to be about 70% of the total green gas emission. Also it consumes large amount of natural resources. Hence it is essential to find alternative to cement. Geopolymer concrete is an innovative material in which the binder is produced but the reaction of an alkaline liquid with a source material that is rich in silica alumina. The present work deals with the result of the experimental investigation carried out on geopolymer concrete using steel fiber. The study analyses the effect of steel on compressive strength. Geopolymer concrete mixes were prepared using low calcium fly ash & activated by alkaline solution. (NaOH & Na2SiO3 with alkaline liquid to fly ash ratio of 0.35 Alkaline solution. Used for present study combination of sodium hydroxide & sodium silicate with ratio 2.5. The mix was designed for molarity of 16M & grade chosen for investigation was M30. Hooked end steel fiber . All tests were conducted according to IS-code procedure. The result for each variation are tabulated & discussed in details & some important conclusions are made.

  7. Nickel-vanadium monolayer double hydroxide for efficient electrochemical water oxidation (United States)

    Fan, Ke; Chen, Hong; Ji, Yongfei; Huang, Hui; Claesson, Per Martin; Daniel, Quentin; Philippe, Bertrand; Rensmo, Håkan; Li, Fusheng; Luo, Yi; Sun, Licheng


    Highly active and low-cost electrocatalysts for water oxidation are required due to the demands on sustainable solar fuels; however, developing highly efficient catalysts to meet industrial requirements remains a challenge. Herein, we report a monolayer of nickel-vanadium-layered double hydroxide that shows a current density of 27 mA cm-2 (57 mA cm-2 after ohmic-drop correction) at an overpotential of 350 mV for water oxidation. Such performance is comparable to those of the best-performing nickel-iron-layered double hydroxides for water oxidation in alkaline media. Mechanistic studies indicate that the nickel-vanadium-layered double hydroxides can provide high intrinsic catalytic activity, mainly due to enhanced conductivity, facile electron transfer and abundant active sites. This work may expand the scope of cost-effective electrocatalysts for water splitting.

  8. Nickel–vanadium monolayer double hydroxide for efficient electrochemical water oxidation (United States)

    Fan, Ke; Chen, Hong; Ji, Yongfei; Huang, Hui; Claesson, Per Martin; Daniel, Quentin; Philippe, Bertrand; Rensmo, Håkan; Li, Fusheng; Luo, Yi; Sun, Licheng


    Highly active and low-cost electrocatalysts for water oxidation are required due to the demands on sustainable solar fuels; however, developing highly efficient catalysts to meet industrial requirements remains a challenge. Herein, we report a monolayer of nickel–vanadium-layered double hydroxide that shows a current density of 27 mA cm−2 (57 mA cm−2 after ohmic-drop correction) at an overpotential of 350 mV for water oxidation. Such performance is comparable to those of the best-performing nickel–iron-layered double hydroxides for water oxidation in alkaline media. Mechanistic studies indicate that the nickel–vanadium-layered double hydroxides can provide high intrinsic catalytic activity, mainly due to enhanced conductivity, facile electron transfer and abundant active sites. This work may expand the scope of cost-effective electrocatalysts for water splitting. PMID:27306541


    Directory of Open Access Journals (Sweden)



    Full Text Available ABSTRACT: AIM: The present study evaluated the antibacterial effec t of calcium hydroxide pastes using four different vehicles namely propylene glycol, glycerin, distilled water and camphorated phenol. MATERIAL AND METHOD: Calcium hydroxide pastes prepared with two commonly used vehicles namely distilled water and c amphorated phenol. The antibacterial activity of these pastes were tested against five a naerobic organism that can commonly occur in the infected root canal. The pastes were also prepare d using two chemicals such as propylene glycol and glycerin. RESULTS AND CONCLUSION: The result of this study show that calcium hydroxide paste made with propylene glycol gives enhan ced antibacterial action and sustains it for longer period of time. Propylene glycol being bi ological acceptable vehicle, it can be recommended for routine use as a vehicle over glyce rin

  10. A role for calcium hydroxide and dolomite in water: acceleration of the reaction under ultraviolet light. (United States)

    Nagase, Hiroyasu; Tsujino, Hidekazu; Kurihara, Daisuke; Saito, Hiroshi; Kawase, Masaya


    Organic environmental pollutants are now being detected with remarkably high frequency in the aquatic environment. Photodegradation by ultraviolet light is sometimes used as a method for removing organic chemicals from water; however, this method is relatively inefficient because of the low degradation rates involved, and more efficient methods are under development. Here we show that the removal of various organic pollutants can be assisted by calcined dolomite in aqueous solution under irradiation with ultraviolet light. It was possible to achieve substantial removal of bisphenol A, chlorophenols, alkylphenols, 1-naphthol and 17β-estradiol. The major component of dolomite responsible for the removal was calcium hydroxide. Our results demonstrate that the use of calcium hydroxide with ultraviolet light irradiation can be a very effective method of rapidly removing organic environmental pollutants from water. This is a new role for calcium hydroxide and dolomite in water treatment.

  11. The effect of crystal orientation on the cryogenic strength of hydroxide catalysis bonded sapphire (United States)

    Haughian, K.; Douglas, R.; van Veggel, A. A.; Hough, J.; Khalaidovski, A.; Rowan, S.; Suzuki, T.; Yamamoto, K.


    Hydroxide catalysis bonding has been used in gravitational wave detectors to precisely and securely join components of quasi-monolithic silica suspensions. Plans to operate future detectors at cryogenic temperatures has created the need for a change in the test mass and suspension material. Mono-crystalline sapphire is one candidate material for use at cryogenic temperatures and is being investigated for use in the KAGRA detector. The crystalline structure of sapphire may influence the properties of the hydroxide catalysis bond formed. Here, results are presented of studies of the potential influence of the crystal orientation of sapphire on the shear strength of the hydroxide catalysis bonds formed between sapphire samples. The strength was tested at approximately 8 K; this is the first measurement of the strength of such bonds between sapphire at such reduced temperatures. Our results suggest that all orientation combinations investigated produce bonds of sufficient strength for use in typical mirror suspension designs, with average strengths >23 MPa.

  12. Electroosmotic dewatering of chalk sludge, iron hydroxide sludge, wet fly ash and biomass sludge

    DEFF Research Database (Denmark)

    Hansen, H.K.; Christensen, Iben Vernegren; Ottosen, Lisbeth M.;


    Electroosmotic dewatering has been tested in laboratory cells on four different porous materials: chalk sludge, iron hydroxide sludge, wet fly ash and biomass sludge from enzyme production. In all cases it was possible to remove water when passing electric DC current through the material. Casagra......Electroosmotic dewatering has been tested in laboratory cells on four different porous materials: chalk sludge, iron hydroxide sludge, wet fly ash and biomass sludge from enzyme production. In all cases it was possible to remove water when passing electric DC current through the material....... Casagrande's coefficients were determined for the four materials at different water contents. The experiments in this work showed that chalk could be dewatered from 40% to 79% DM (dry matter), fly ash from 75 to 82% DM, iron hydroxide sludge from 2.7 to 19% DM and biomass from 3 to 33% DM by electroosmosis...

  13. Large-scale Hydrothermal Synthesis and Characterization of Size-controlled Lanthanum Hydroxide Nanorods

    Institute of Scientific and Technical Information of China (English)

    YI,Ran; ZHANG,Ning; SHI,Rongrong; LI,Yongbo; QIU Guanzhou; LIU Xiaohe


    Uniform lanthanum hydroxide nanorods were successfully synthesized in large quantities through a facile hydrothermal synthetic method, in which soluble lanthanum nitrate was used to supply the lanthanum source and triethylamine (TEA) was used as both alkaline agent and complexing agent. The influences of triethylamine amount, surfactant, reaction temperature and time on the size and shape of lanthanum hydroxide nanorods were investigated in detail. Trivalent rare earth ion doped lanthanum hydroxide nanorods were also obtained in this paper. The phase structures and morphologies of the as-prepared products were investigated in detail by X-ray diffraction (XRD), transmission electron microscopy (TEM), selected area electron diffraction (SAED) and high-resolution transmis-sion electron microscopy (HRTEM). The probable formation mechanism was proposed based on the experimental results.

  14. Removal of Indigo Carmine Dye from Aqueous Solution Using Magnesium Hydroxide as an Adsorbent

    Directory of Open Access Journals (Sweden)

    Thimmasandra Narayan Ramesh


    Full Text Available Magnesium hydroxide is used as an adsorbent for the removal of indigo carmine dye from aqueous solution. We have investigated the effectiveness of removal of indigo carmine dye from aqueous solutions at pH 6-7 and 12-13 using magnesium hydroxide thereby varying the dose of the adsorbent, concentration of the dye, duration, and temperature. Structural transformations of adsorbent during the adsorption process at different pH values are monitored using powder X-ray diffraction and infrared spectroscopy. Different types of adsorption isotherm models were evaluated and it was found that Langmuir isotherm fits well at both pH values (6-7 and 12-13. Adsorption of indigo carmine onto magnesium hydroxide at pH 6-7/pH 12-13 follows pseudo-second order rate kinetics.

  15. Aluminum phosphate shows more adjuvanticity than Aluminum hydroxide in recombinant hepatitis –B vaccine formulation

    Directory of Open Access Journals (Sweden)


    Full Text Available Background: Although a number of investigation have been carried out to find alternative adjuvants to aluminum salts in vaccine formulations, they are still extensively used due to their good track record of safety, low cost and proper adjuvanticity with a variety of antigens. Adsorption of antigens onto aluminum compounds depends heavily on electrostatic forces between adjuvant and antigen. Commercial recombinant protein hepatitis B vaccines containing aluminum hydroxide as adjuvant is facing low induction of immunity in some sections of the vaccinated population. To follow the current global efforts in finding more potent hepatitis B vaccine formulation, adjuvanticity of aluminum phosphate has been compared to aluminum hydroxide. Materials and methods: The adjuvant properties of aluminum hydroxide and aluminum phosphate in a vaccine formulation containing a locally manufactured hepatitis B (HBs surface antigen was evaluated in Balb/C mice. The formulations were administered intra peritoneally (i.p. and the titers of antibody which was induced after 28 days were determined using ELISA technique. The geometric mean of antibody titer (GMT, seroconversion and seroprotection rates, ED50 and relative potency of different formulations were determined. Results: All the adjuvanicity markers obtained in aluminum phosphate formulation were significantly higher than aluminum hydroxide. The geometric mean of antibody titer of aluminum phosphate was approximately three folds more than aluminum hydroxide. Conclusion: Aluminum phosphate showed more adjuvanticity than aluminum hydroxide in hepatitis B vaccine. Therefore the use of aluminum phosphate as adjuvant in this vaccine may lead to higher immunity with longer duration of effects in vaccinated groups.

  16. Three Alkali-Rich Intrusive Rock Belts Newly Discovered in the Mt. Kunlun-Mt. Altun Region, Xinjiang, China

    Institute of Scientific and Technical Information of China (English)

    朱笑青; 王元龙; 毕华; 王中刚


    The newly discovered three alkali-rich intrusive rock belts in the Mt. Kunlun Mt.Altun region of southern Xinjiang are the Lapeiquan-Yitunbulak alkali-rich intrusive rock belt,the Gez-Taxkorgan alkali-rich intrusive rock belt and the Beilisai-Abulash alkali-rich intrusive rock belt. The former two belts were formed during the Yanshanian period, and the third one was formed during the Himalayan period, which is the youngest alkali-rich intrusive rock belt in China. The discovery of the alkali-rich intrusive rock belts is of great significance in shedding light on the history of tectono-magmatic activities in this region.

  17. Preparation of hydroxide ion conductive KOH–layered double hydroxide electrolytes for an all-solid-state iron–air secondary battery

    Directory of Open Access Journals (Sweden)

    Taku Tsuneishi


    Full Text Available Anion conductive solid electrolytes based on Mg–Al layered double hydroxide (LDH were prepared for application in an all-solid-state Fe–air battery. The ionic conductivity and the conducting ion species were evaluated from impedance and electromotive force measurements. The ion conductivity of LDH was markedly enhanced upon addition of KOH. The electromotive force in a water vapor concentration cell was similar to that of an anion-conducting polymer membrane. The KOH–LDH obtained was used as a hydroxide ion conductive electrolyte for all-solid-state Fe–air batteries. The cell performance of the Fe–air batteries was examined using a mixture of KOH–LDH and iron-oxide-supported carbon as the negative electrode.

  18. Double-Shelled Nanocages with Cobalt Hydroxide Inner Shell and Layered Double Hydroxides Outer Shell as High-Efficiency Polysulfide Mediator for Lithium-Sulfur Batteries. (United States)

    Zhang, Jintao; Hu, Han; Li, Zhen; Lou, Xiong Wen David


    Lithium-sulfur (Li-S) batteries have been considered as a promising candidate for next-generation electrochemical energy-storage technologies because of their overwhelming advantages in energy density. Suppression of the polysulfide dissolution while maintaining a high sulfur utilization is the main challenge for Li-S batteries. Here, we have designed and synthesized double-shelled nanocages with two shells of cobalt hydroxide and layered double hydroxides (CH@LDH) as a conceptually new sulfur host for Li-S batteries. Specifically, the hollow CH@LDH polyhedra with complex shell structures not only maximize the advantages of hollow nanostructures for encapsulating a high content of sulfur (75 wt %), but also provide sufficient self-functionalized surfaces for chemically bonding with polysulfides to suppress their outward dissolution. When evaluated as cathode material for Li-S batteries, the CH@LDH/S composite shows a significantly improved electrochemical performance.

  19. Antimycobacterial, antimicrobial, and biocompatibility properties of para-aminosalicylic acid with zinc layered hydroxide and Zn/Al layered double hydroxide nanocomposites. (United States)

    Saifullah, Bullo; El Zowalaty, Mohamed E; Arulselvan, Palanisamy; Fakurazi, Sharida; Webster, Thomas J; Geilich, Benjamin M; Hussein, Mohd Zobir


    The treatment of tuberculosis by chemotherapy is complicated due to multiple drug prescriptions, long treatment duration, and adverse side effects. We report here for the first time an in vitro therapeutic effect of nanocomposites based on para-aminosalicylic acid with zinc layered hydroxide (PAS-ZLH) and zinc-aluminum layered double hydroxides (PAS-Zn/Al LDH), against mycobacteria, Gram-positive bacteria, and Gram-negative bacteria. The nanocomposites demonstrated good antimycobacterial activity and were found to be effective in killing Gram-positive and Gram-negative bacteria. A biocompatibility study revealed good biocompatibility of the PAS-ZLH nanocomposites against normal human MRC-5 lung cells. The para-aminosalicylic acid loading was quantified with high-performance liquid chromatography analysis. In summary, the present preliminary in vitro studies are highly encouraging for further in vivo studies of PAS-ZLH and PAS-Zn/Al LDH nanocomposites to treat tuberculosis.

  20. Cobalt hydroxide/oxide hexagonal ring-graphene hybrids through chemical etching of metal hydroxide platelets by graphene oxide: energy storage applications. (United States)

    Nethravathi, C; Rajamathi, Catherine R; Rajamathi, Michael; Wang, Xi; Gautam, Ujjal K; Golberg, Dmitri; Bando, Yoshio


    The reaction of β-Co(OH)2 hexagonal platelets with graphite oxide in an aqueous colloidal dispersion results in the formation of β-Co(OH)2 hexagonal rings anchored to graphene oxide layers. The interaction between the basic hydroxide layers and the acidic groups on graphene oxide induces chemical etching of the hexagonal platelets, forming β-Co(OH)2 hexagonal rings. On heating in air or N2, the hydroxide hybrid is morphotactically converted to porous Co3O4/CoO hexagonal ring-graphene hybrids. Porous NiCo2O4 hexagonal ring-graphene hybrid is also obtained through a similar process starting from β-Ni0.33Co0.67(OH)2 platelets. As electrode materials for supercapacitors or lithium-ion batteries, these materials exhibit a large capacity, high rate capability, and excellent cycling stability.

  1. Development of Drug Delivery Systems Based on Layered Hydroxides for Nanomedicine

    Directory of Open Access Journals (Sweden)

    Farahnaz Barahuie


    Full Text Available Layered hydroxides (LHs have recently fascinated researchers due to their wide application in various fields. These inorganic nanoparticles, with excellent features as nanocarriers in drug delivery systems, have the potential to play an important role in healthcare. Owing to their outstanding ion-exchange capacity, many organic pharmaceutical drugs have been intercalated into the interlayer galleries of LHs and, consequently, novel nanodrugs or smart drugs may revolutionize in the treatment of diseases. Layered hydroxides, as green nanoreservoirs with sustained drug release and cell targeting properties hold great promise of improving health and prolonging life.

  2. Studies on Thorium Adsorption Characteristics upon Activated Titanium Hydroxide Prepared from Rosetta Ilmenite Concentrate

    Energy Technology Data Exchange (ETDEWEB)

    Gado, M, E-mail:; Zaki, S [Nuclear Materials Authority, P. O. Box 530 El Maadi, Cairo (Egypt)


    The titanium hydroxide prepared from Rosetta ilmenite concentrate has been applied for Th (IV) adsorption from its acid aqueous solutions. The prepared hydroxide is first characterized by both Fourier transform infrared (FT-IR) spectrum and thermogravimetric analysis. The relevant factors affecting the adsorption process have been studied. The obtained equilibrium data fits well with the Langmuir isotherm rather than Freundlich isotherm, while the adsorption kinetic data follow the pseudo-second order model. The different thermodynamic parameters have also been calculated and indicate that the adsorption process is spontaneous.

  3. Sulfur removal from Gediz lignite using aqueous sodium hydroxide solutions under mild oxidative conditions

    Energy Technology Data Exchange (ETDEWEB)

    Yaman, S.; Kuecuekbayrak, S. [Istanbul Technical Univ. (Turkey). Chemical and Metallurgical Engineering Faculty


    Sulfur removal from a high-sulfur Turkish lignite (Gediz) using aqueous sodium hydroxide solutions having dissolved oxygen was investigated under mild oxidative conditions. Effects of the parameters such as sodium hydroxide/lignite weight ratio, temperature, and partial pressure of oxygen were investigated within the ranges of 0.05--0.8, 423--498 K, and 1--2 MPa, respectively. Optimum values of these parameters were determined regarding sulfur removal and coal recovery. Influences of dry oxidation of the lignite sample as a pretreatment at 573 K and subsequent washing of some treated lignite samples with 1 N HCl were investigated.

  4. Synthesis and Characterization of Layered Double Hydroxides Containing Optically Active Transition Metal Ion (United States)

    Tyagi, S. B.; Kharkwal, Aneeta; Nitu; Kharkwal, Mamta; Sharma, Raghunandan


    The acetate intercalated layered double hydroxides of Zn and Mn, have been synthesized by chimie douce method. The materials were characterized by XRD, TGA, CHN, IR, XPS, SEM-EDX and UV-visible spectroscopy. The photoluminescence properties was also studied. The optical properties of layered hydroxides are active transition metal ion dependent, particularly d1-10 system plays an important role. Simultaneously the role of host - guest orientation has been considered the basis of photoluminescence. Acetate ion can be exchanged with iodide and sulphate ions. The decomposed product resulted the pure phase Mn doped zinc oxide are also reported.

  5. Synthesis, characterization and stability of Cr(III) and Fe(III) hydroxides. (United States)

    Papassiopi, N; Vaxevanidou, K; Christou, C; Karagianni, E; Antipas, G S E


    Chromium is a common contaminant of soils and aquifers and constitutes a major environmental problem. In nature, chromium usually exists in the form of two oxidation states, trivalent, Cr(III), which is relatively innocuous for biota and for the aquatic environment, and hexavalent, Cr(VI) which is toxic, carcinogenic and very soluble. Accordingly, the majority of wastewater and groundwater treatment technologies, include a stage where Cr(VI) is reduced to Cr(III), in order to remove chromium from the aqueous phase and bind the element in the form of environmentally stable solid compounds. In the absence of iron the final product is typically of the form Cr(OH)3·xH2O whereas in the presence of iron the precipitate is a mixed Fe(1-x)Crx(OH)3 phase. In this study, we report on the synthesis, characterisation and stability of mixed (Fex,Cr1-x)(OH)3 hydroxides as compared to the stability of Cr(OH)3. We established that the plain Cr(III) hydroxide, abiding to the approximate molecular formula Cr(OH)3·3H2O, was crystalline, highly soluble, i.e. unstable, with a tendency to transform into the stable amorphous hydroxide Cr(OH)3(am) phase. Mixed Fe0.75Cr0.25(OH)3 hydroxides were found to be of the ferrihydrite structure, Fe(OH)3, and we correlated their solubility to that of a solid solution formed by plain ferrihydrite and the amorphous Cr(III) hydroxide. Both our experimental results and thermodynamic calculations indicated that mixed Fe(III)-Cr(III) hydroxides are more effective enhancers of groundwater quality, in comparison to the plain amorphous or crystalline Cr(III) hydroxides, the latter found to have a solubility typically higher than 50μg/l (maximum EU permitted Cr level in drinking water), while the amorphous Cr(OH)3(am) phase was within the drinking water threshold in the range 5.7hydroxides studied were of extended stability in the 4.8

  6. Large-scale simulations of layered double hydroxide nanocomposite materials (United States)

    Thyveetil, Mary-Ann

    Layered double hydroxides (LDHs) have the ability to intercalate a multitude of anionic species. Atomistic simulation techniques such as molecular dynamics have provided considerable insight into the behaviour of these materials. We review these techniques and recent algorithmic advances which considerably improve the performance of MD applications. In particular, we discuss how the advent of high performance computing and computational grids has allowed us to explore large scale models with considerable ease. Our simulations have been heavily reliant on computational resources on the UK's NGS (National Grid Service), the US TeraGrid and the Distributed European Infrastructure for Supercomputing Applications (DEISA). In order to utilise computational grids we rely on grid middleware to launch, computationally steer and visualise our simulations. We have integrated the RealityGrid steering library into the Large-scale Atomic/Molecular Massively Parallel Simulator (LAMMPS) 1 . which has enabled us to perform re mote computational steering and visualisation of molecular dynamics simulations on grid infrastruc tures. We also use the Application Hosting Environment (AHE) 2 in order to launch simulations on remote supercomputing resources and we show that data transfer rates between local clusters and super- computing resources can be considerably enhanced by using optically switched networks. We perform large scale molecular dynamics simulations of MgiAl-LDHs intercalated with either chloride ions or a mixture of DNA and chloride ions. The systems exhibit undulatory modes, which are suppressed in smaller scale simulations, caused by the collective thermal motion of atoms in the LDH layers. Thermal undulations provide elastic properties of the system including the bending modulus, Young's moduli and Poisson's ratios. To explore the interaction between LDHs and DNA. we use molecular dynamics techniques to per form simulations of double stranded, linear and plasmid DNA up

  7. Antimycobacterial, antimicrobial, and biocompatibility properties of para-aminosalicylic acid with zinc layered hydroxide and Zn/Al layered double hydroxide nanocomposites

    Directory of Open Access Journals (Sweden)

    Saifullah B


    Full Text Available Bullo Saifullah,1 Mohamed E El Zowalaty,2,3 Palanisamy Arulselvan,2 Sharida Fakurazi,2,4 Thomas J Webster,5,6 Benjamin M Geilich,5 Mohd Zobir Hussein1 1Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology (ITMA, Universiti Putra Malaysia, Serdang, Selangor, Malaysia; 2Laboratory of Vaccines and Immunotherapeutics, Institute of Bioscience, Universiti Putra Malaysia, Serdang, Selangor, Malaysia; 3Department of Environmental Health, Faculty of Public Health and Tropical Medicine, Jazan University, Jazan, Saudi Arabia; 4Department of Human Anatomy, Faculty of Medicine and Health Science, Universiti Putra Malaysia, Serdang, Selangor, Malaysia; 5Department of Chemical Engineering and Program in Bioengineering, Northeastern University, Boston, MA, USA; 6Center of Excellence for Advanced Materials Research, King Abdulaziz University, Jeddah, Saudi Arabia Abstract: The treatment of tuberculosis by chemotherapy is complicated due to multiple drug prescriptions, long treatment duration, and adverse side effects. We report here for the first time an in vitro therapeutic effect of nanocomposites based on para-aminosalicylic acid with zinc layered hydroxide (PAS-ZLH and zinc-aluminum layered double hydroxides (PAS-Zn/Al LDH, against mycobacteria, Gram-positive bacteria, and Gram-negative bacteria. The nanocomposites demonstrated good antimycobacterial activity and were found to be effective in killing Gram-positive and Gram-negative bacteria. A biocompatibility study revealed good biocompatibility of the PAS-ZLH nanocomposites against normal human MRC-5 lung cells. The para-aminosalicylic acid loading was quantified with high-performance liquid chromatography analysis. In summary, the present preliminary in vitro studies are highly encouraging for further in vivo studies of PAS-ZLH and PAS-Zn/Al LDH nanocomposites to treat tuberculosis.  Keywords: Zn/Al-layered double hydroxides, zinc layered hydroxides, tuberculosis, para

  8. 稀碱预处理棕榈残渣制备纤维乙醇%Pretreatment of oil palm residues by dilute alkali for cellulosic ethanol production

    Institute of Scientific and Technical Information of China (English)

    张海燕; 周玉杰; 李晋平; 戴玲妹; 刘德华; 张建安; Yuen May Choo; Soh Kheang Loh


    In the study, we used oil palm residues (empty fruit bunch, EFB) as raw material to produce cellulosic ethanol by pretreatment, enzymatic hydrolysis and fermentation. Firstly, the pretreatment of EFB with alkali, alkali/hydrogen peroxide and the effects on the components and enzymatic hydrolysis of cellulose were studied. The results show that dilute alkali was the suitable pretreatment method and the conditions were first to soak the substrate with 1% sodium hydroxide with a solid-liquid ratio of 1:10 at 40 ℃ for 24 h, and then subjected to 121 ℃ for 30 min. Under the conditions, EFB solid recovery was 74.09%, and glucan, xylan and lignin content were 44.08%, 25.74% and 13.89%, respectively. After separated with alkali solution, the pretreated EFB was washed and hydrolyzed for 72 h with 5% substrate concentration and 30 FPU/g dry mass (DM) enzyme loading, and the conversion of glucan and xylan reached 84.44% and 89.28%, respectively. We further investigated the effects of substrate concentration and enzyme loading on enzymatic hydrolysis and ethanol batch simultaneous saccharification and fermentation (SSF). The results show that when enzyme loading was 30 FPU/g DM and substrate concentration was increased from 5% to 25%, ethanol concentration were 9.76 g/L and 35.25 g/L after 72 h fermentation with Saccharomyces cerevisiae (inoculum size 5%, V/V), which was 79.09% and 56.96% of ethanol theory yield.%以棕榈残渣(Empty fruit bunch,EFB)为原料,通过预处理、酶解、发酵等过程制备纤维乙醇.首先对比了碱、碱/过氧化氢等预处理条件对棕榈残渣组成及酶解的影响,结果表明稀碱预处理效果较好.适宜的稀碱预处理条件为:NaOH浓度为1%,固液比为1∶10,在40℃浸泡24 h后于121℃下保温30 min,在该条件下,EFB的固体回收率为74.09%,纤维素、半纤维素和木质素的含量分别为44.08%、25.74%和13.89%.对该条件下预处理后的固体样品,以底物浓度5

  9. A facile one-pot synthesis of ruthenium hydroxide nanoparticles on magnetic silica: Aqueous hydration of nitriles to amides (United States)

    One-pot synthesis of ruthenium hydroxide nanoparticles on magnetic silica is described which involve the in situ generation of magnetic silica (Fe3O4@ SiO2) and ruthenium hydroxide immobilization; the hydration of nitriles occurs in high yield and excellent selectivity using this...

  10. Hg soil pollution around the Flix chlor-alkali plant (United States)

    Esbrí, José Maria; López-Berdoces, Miguel Angel; Martínez-Coronado, Alba; Fernández-Calderon, Sergio; Díez, Sergi; León Higueras, Pablo


    Main mercury consumer in industrialized countries is the chlor-alkali industry. In Spain, this industry declares 2.54 tons of mercury emissions to the atmosphere per year, but the losses of mercury in this industrial process seem to be higher than this. In the next 15 years, these industries are going to make a technology change to a free mercury based technology. This study has been applied to the Flix (Tarragona, NE Spain) plant, located very near the Ebro River. Local industrial activity started in the late 18th Century, being the first Spanish industrial precinct in activity. Technology used in this plant is obsolete, and produces important emissions to the atmosphere. Besides, it has also produced an important pollution problem in the Ebro River. The aim of this work is the characterization of mercury soil pollution around the oldest chlor-alkali plant (CAP), actually in process of decommissioning. For this porpoises, we provided data of mercury in soils and in olive oil leaves, in order to assess the extent of this pollution, and the consequences in terms of transferring to local agricultural biota. We present data from two soils geochemistry surveys, one centered in the general area, and a second one centered in an anomalous area identified by the first survey, at the Ebro margins downstream the town area. A total of 126 surface soil samples were taken and analyzed for total mercury by means of a Lumex RA-915+ device with RP- 91C pyrolysis attachment. Soil-plant transfer was studied based on mercury contents in olive leaves, the most ubiquitous plant species in the area; these biological samples were thoroughly clean and freeze-dried before its total mercury analysis in a Lumex RA-915+ device with its RP-91c pyrolysis attachment. Mercury contents in soils reach maximum levels in the vicinity of CAP (495 mg kg-1), much higher than baseline levels found in the area (0.18 mg kg-1, in average). These polluted soils are located near CAP and the riverbanks of Ebro

  11. Hydrogen Adsorption by Alkali Metal Graphite Intercalation Compounds (United States)

    Purewal, Justin

    Adsorption occurs whenever a solid surface is exposed to a gas or liquid, and is characterized by an increase in fluid density near the interface. Adsorbents have drawn attention in the current effort to engineer materials that store hydrogen at high densities within moderate temperature and pressure regimes. Carbon adsorbents are a logical choice as a storage material due to their low costs and large surface areas. Unfortunately, carbon adsorbents suffer from a low binding enthalpy for H2 (about 5 kJ mol-1), well below the 15 to 18 kJ mol-1) that is considered optimal for hydrogen storage systems. Binding interactions can be increased by the following methods: (1) adjusting the graphite interplanar separation with a pillared structure, and (2) introducing dopant species that interact with H2 molecules by strong electrostatic forces. Graphite intercalation compounds are a class of materials that contain both pillared structures and chemical dopants, making them an excellent model system for studying the fundamentals of hydrogen adsorption in nanostructured carbons. Pressure-composition-temperature diagrams of the MC24(H 2)x graphite intercalation compounds were measured for M = (K, Rb, Cs). Adsorption enthalpies were measured as a function of H2 concentration. Notably, CsC24 had an average adsorption enthalpy of 14.9 kJ mol-1), nearly three times larger than that of pristine graphite. The adsorption enthalpies were found to be positively correlated with the alkali metal size. Adsorption capacities were negatively correlated with the size of the alkali metal. The rate of adsorption is reduced at large H2 compositions, due to the effects of site-blocking and correlation on the H2 diffusion. The strong binding interaction and pronounced molecular-sieving behavior of KC24 is likely to obstruct the translational diffusion of adsorbed H2 molecules. In this work, the diffusion of H2 adsorbed in KC24 was studied by quasielastic neutron scattering measurements and molecular

  12. Comparison of ionomic and metabolites response under alkali stress in old and young leaves of cotton (Gossypium hirsutum L. seedlings

    Directory of Open Access Journals (Sweden)

    Rui Guo


    Full Text Available Soil salinization is an important agriculture-related environmental problem. Alkali stress and salt stress strongly influence the metabolic balance in plants. Salt and alkali stresses exert varied effects on old and young tissues, which display different adaptive strategies. In this study, we used cotton (Gossypium hirsutum L. plants as experimental material to investigate whether alkali stress exerts varied effects on ion balance and metabolism in old and young leaves of cotton plants exposed to alkali stress. Moreover, we compared the functions of young and old leaves in alkali tolerance. Results showed that alkali stress exerted a considerably stronger growth inhibition on old leaves than on young leaves. Under alkali stress, young leaves can maintain low Na and high K contents and retain relatively stable pigment accumulation and tricarboxylic acid cycle (TCA, resulting in greater accumulation of photosynthetic metabolites. In terms of metabolic response, the young and old leaves clearly displayed different mechanisms of osmotic regulation. The amounts of inositol and mannose significantly increased in both old and young leaves of cotton exposed to alkali stress, and the extent of increase was higher in young leaves than in old leaves. In old leaves, synthesis of amino acids, such as GABA, valine, and serine, was dramatically enhanced, and this phenomenon is favorable for osmotic adjustment and membrane stability. Organs at different developmental stages possibly display different mechanisms of metabolic regulation under stress condition. Thus, we propose that future investigations on alkali stress should use more organs obtained at different developmental stages.

  13. Novel, inorganic composites using porous, alkali-activated, aluminosilicate binders (United States)

    Musil, Sean

    Geopolymers are an inorganic polymeric material composed of alumina, silica, and alkali metal oxides. Geopolymers are chemical and fire resistant, can be used as refractory adhesives, and are processed at or near ambient temperature. These properties make geopolymer an attractive choice as a matrix material for elevated temperature composites. This body of research investigated numerous different reinforcement possibilities and variants of geopolymer matrix material and characterized their mechanical performance in tension, flexure and flexural creep. Reinforcements can then be chosen based on the resulting properties to tailor the geopolymer matrix composites to a specific application condition. Geopolymer matrix composites combine the ease of processing of polymer matrix composites with the high temperature capability of ceramic matrix composites. This study incorporated particulate, unidirectional fiber and woven fiber reinforcements. Sodium, potassium, and cesium based geopolymer matrices were evaluated with cesium based geopolymer showing great promise as a high temperature matrix material. It showed the best strength retention at elevated temperature, as well as a very low coefficient of thermal expansion when crystallized into pollucite. These qualities made cesium geopolymer the best choice for creep resistant applications. Cesium geopolymer binders were combined with unidirectional continuous polycrystalline mullite fibers (Nextel(TM) 720) and single crystal mullite fibers, then the matrix was crystallized to form cubic pollucite. Single crystal mullite fibers were obtained by the internal crystallization method and show excellent creep resistance up to 1400°C. High temperature flexural strength and flexural creep resistance of pollucite and polycrystalline/single-crystal fibers was evaluated at 1000-1400°C.

  14. Crystallization Behaviour and Nanostructuring in Alkali Niobiosilicate Glasses

    Institute of Scientific and Technical Information of China (English)

    E.Fanelli; P.Pernice; M.Xiao; A.Aronne; V.N.Sigacv


    23K2O·27Nb2O5·50SiO2 (KNS), 13K2O·10Na2O·27Nb2C5·50SiO2 (KNaNS) and 15K2O·12Li2O·27Nb2O5· 46SiO2 (KLiNS) transparent glasses were synthesized by melt-quenching technique, and studied by differential thermal analysis (DTA), X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM) to reveal the effect of the devitrification behaviour on transparent nanostructure.Just above the glass transition temperature Tg in the KNS glass, an unidentified phase was formed, while in KNaNS and KLiNS, mixed-alkali niobate phases with tungsten bronze structure were obtained by bulk crystallization.Heat treatments at Tg performed on the KNS glass resulted in the transparent nanostructure with second order harmonic generation (SHG) activity.Heat treatment for 10 h on KNaNS and KLiNS decreased the first DTA exothermic peaks (at least 24℃), indicating the bulk nucleation, which was confirmed by the DTA in comparison with the powdered as-quenched samples.KNaNS and KLiNS showed similar XRD profiles as the K3Li2Nb5O15 crystal with the five most intense peaks at 22.7, 29.4, 32.3, 46.3 and 52.0 deg.HRTEM micrograph showed clear-cut nano-sized circular domains and spherical nanocrystals dispersed into the amorphous matrix.

  15. On the origin of alkali metals in Europa exosphere (United States)

    Ozgurel, Ozge; Pauzat, Françoise; Ellinger, Yves; Markovits, Alexis; Mousis, Olivier; LCT, LAM


    At a time when Europa is considered as a plausible habitat for the development of an early form of life, of particular concern is the origin of neutral sodium and potassium atoms already detected in its exosphere (together with magnesium though in smaller abundance), since these atoms are known to be crucial for building the necessary bricks of prebiotic species. However their origin and history are still poorly understood. The most likely sources could be exogenous and result from the contamination produced by Io's intense volcanism and/or by meteoritic bombardment. These sources could also be endogenous if these volatile elements originate directly from Europa's icy mantle. Here we explore the possibility that neutral sodium and potassium atoms were delivered to the satellite's surface via the upwelling of ices formed in contact with the hidden ocean. These metallic elements would have been transferred as ions to the ocean at early epochs after Europa's formation, by direct contact of water with the rocky core. During Europa's subsequent cooling, the icy layers formed at the top of the ocean would have kept trapped the sodium and potassium, allowing their future progression to the surface and final identification in the exosphere of the satellite. To support this scenario, we have used chemistry numerical models based on first principle periodic density functional theory (DFT). These models are shown to be well adapted to the description of compact ice and are capable to describe the trapping and neutralization of the initial ions in the ice matrix. The process is found relevant for all the elements considered, alkali metals like Na and K, as well as for Mg and probably for Ca, their respective abundances depending essentially of their solubility and chemical capabilities to blend with water ices.

  16. Assessment of alkali metal coolants for the ITER blanket (United States)

    Natesan, K.; Reed, C. B.; Mattas, R. F.


    The blanket system is one of the most important components of a fusion reactor because it has a major impact on both the economics and safety of fusion energy. The primary functions of the blanket in a deuterium/tritium-fueled fusion reactor are to convert the fusion energy into sensible heat and to breed tritium for the fuel cycle. The blanket comparison and selection study, conducted earlier, described the overall comparative performance of different blanket concepts, including liquid metal, molten salt, water, and helium. This paper will discuss the ITER requirements for a self-cooled blanket concept with liquid lithium and for indirectly cooled concepts that use other alkali metals such as NaK. The paper addresses the thermodynamics of interactions between the liquid metals (e.g., lithium and NaK) and structural materials (e.g., V-base alloys), together with associated corrosion/compatibility issues. Available experimental data are used to assess the long-term performance of the first wall in a liquid metal environment. Other key issues include development of electrical insulator coatings on the first-wall structural material to MHD pressure drop, and tritium permeation/inventory in self-cooled and indirectly cooled concepts. Acceptable types of coatings (based on their chemical compatibility and physical properties) are identified, and surface-modification avenues to achieve these coatings on the first wall are discussed. The assessment examines the extent of our knowledge on structural materials performance in liquid metals and identifies needed research and development in several of the areas in order to establish performance envelopes for the first wall in a liquid-metal environment.

  17. Rice husk ash as a source of silica in alkali-activated fly ash and granulated blast furnace slag systems

    Directory of Open Access Journals (Sweden)

    Mejía, J. M.


    Full Text Available This study assesses the viability of using an agro-industrial by-product, rice husk ash (RHA from a Colombian rice company’s combustion facility, as a total replacement for the commercial sodium silicate ordinarily used in alkaliactivated binders. Fly ash (FA, granulated blast furnace slag (GBFS and binary 50FA:50GBFS blended pastes were activated with a mix of sodium hydroxide and either sodium silicate or one of two types of RHA. The pastes were characterised for strength, mineralogy and microstructure. The findings showed that the agro-industrial by-product can be used to yield alkali-activated materials with 7-day mechanical strengths on the order of 42 MPa. The study confirmed that both amorphous silica and part of the crystalline silica present in RHA participate in the alkaline activation process, providing the alkalinity is suitably adjusted.Este estudio evalúa la viabilidad de utilizar un subproducto agroindustrial, la ceniza de cascarilla de arroz (RHA proveniente de un equipo combustor de una empresa Arrocera en Colombia, como reemplazo total de la sílice aportada por el silicato de sodio comercial en sistemas cementicios activados alcalinamente. Se prepararon pastas de ceniza volante (FA, de escoria de alto horno (GBFS y un sistema binario 50FA:50GBFS, que fueron activadas por una mezcla de silicato de sodio e hidróxido de sodio, y por dos tipos de RHA. Las mezclas se caracterizaron mecánica, mineralógica y microestructuralmente. Los resultados demuestran que es posible obtener materiales activados alcalinamente con resistencias mecánicas del orden de 42 MPa, a 7 días de curado, utilizando el subproducto agroindustrial. Este estudio corrobora que tanto la sílice amorfa como parte de la sílice cristalina presente en RHA tienen la posibilidad de participar en el proceso de activación alcalina, siempre y cuando las condiciones de alcalinidad estén adecuadamente ajustadas.

  18. Catalytic wet peroxide oxidation of azo dye (Direct Blue 15) using solvothermally synthesized copper hydroxide nitrate as catalyst. (United States)

    Zhan, Yuzhong; Zhou, Xiang; Fu, Bei; Chen, Yiliang


    Copper hydroxide nitrate (Cu(2)(OH)(3)NO(3)) was synthesized solvothermally in anhydrous ethanol and characterized by XRD, FTIR, TG-DTA and SEM. The peroxide degradation of an azo dye (Direct Blue 15) on this material was evaluated by examining catalyst loading, initial pH, hydrogen peroxide dosage, initial dye concentration and temperature. The leaching of Cu from the copper hydroxide nitrate during the reaction was also measured. The copper hydroxide nitrate synthesized solvothermally, which was of a novel spherical morphology with complex secondary structures and contained high-dispersed Cu(2)O impurity, showed good performance for oxidation degradation of the azo dye, especially high catalytic activity, high utilization of hydrogen peroxide and a wide pH range, whereas the copper hydroxide nitrate synthesized by the direct reaction of copper nitrate and sodium hydroxide showed low catalytic activity.

  19. Utilization of Magnesium Hydroxide Produced by Magnesia Hydration as Fire Retardant for Nylon 6-6,6

    Directory of Open Access Journals (Sweden)

    Rocha Sônia D.F.


    Full Text Available The present work investigates the use of magnesium hydroxide, produced by magnesia hydration, as a fire retardant in polymers. The hydration was carried out in an autoclave, at temperature of 130°C for 1 hour, and the product was further submitted to cominution in a jet mill. The solids were characterized with regard to their chemical composition, particle size distribution, surface area and morphology. The performance evaluation of the hydroxide as a flame retardant for a copolymer of nylon 6-6,6 was carried out according to the UL94 specifications for vertical burning tests. V-0 flammability rating at 1.6 mm (60% magnesium hydroxide-filled nylon composite and at 3.2 mm (40% magnesium hydroxide filled nylon composite were achieved. Mechanical properties were maintained at the desired values. These results indicate that the hydroxide obtained from magnesia hydration can be successfully employed as a fire retardant for nylon 6-6,6.

  20. 双(羟基)金属复合氧化物的表面改性%Surface Modification of Layered Double Hydroxide

    Institute of Scientific and Technical Information of China (English)

    冯春瑶; 矫庆泽; 李蕾; 张春英; 段雪


    Mg/Al layered double hydroxide(LDH) was treated with stearic acid by a wet method. The modified double hydroxide showed good dispersion and floatation property with their layer structure being remained almost unchanged.