Potentiodynamic characteristics of cadmium and silver in alkaline solutions

International Nuclear Information System (INIS)

Saidman, S.B.; Vilche, J.R.; Arvia, A.J.; Lopes Teijelo, M.

1984-01-01

The potentiodynamic and ellipsometric characteristics of cadmium and silver in alkaline solutions are studied. The phenomenology of both electrodes shows some common features which are interpreted in termo of a complex hydrated oxide anodic film structure resulting from simultaneous electrochemical and chemical reactions. The kinetics of film growth fits the predictions of nucleation and growth models. (C.L.B.) [pt

Selective solvation extraction of gold from alkaline cyanide solution by alkyl phosphorus esters

Energy Technology Data Exchange (ETDEWEB)

Miller, J.D.; Wan, R.Y.; Mooiman, M.B.; Sibrell, P.L.

1987-01-01

Research efforts have shown that solvation extraction of gold from alkaline cyanide solution is possible by alkyl phosphorus esters. Both tributyl phosphate (TBP) and dibutyl butyl phosphonate (DBBP) appear to be effective extractants for gold and exhibit high loading capacities exceeding 30 gpl. Selective solvation extraction of gold from alkaline cyanide solution can be achieved with selectivity factors relative to other cyanoanions as high as 1000 under certain circumstances. Variables influencing the selectivity such as ionic strength, temperature, and extractant structure, are discussed in terms of the extraction chemistry, which seems to involve the solvation of a M dot, dot, dot Au(CN)2 ion pair.

Addition and elimination kinetics in OH radical induced oxidation of phenol and cresols in acidic and alkaline solutions

International Nuclear Information System (INIS)

Roder, M.; Wojnarovits, L.; Foeldiak, G.; Emmi, S.S.; Beggiato, G.; D'Angelantonio, M.

1999-01-01

The rates of the two consecutive reactions, OH radical addition and H 2 O/OH - elimination, were studied by pulse radiolysis in highly acidic (pH=1.3-1.9) and alkaline (pH∼11) solutions, respectively, for phenol and for the three cresol isomers. The rate coefficient of the addition as measured by the build-up of phenoxyl radical absorbance and by a competitive method is the same (1.4±0.1)x10 10 mol -1 dm 3 s -1 both in acidic and alkaline solution. The rate coefficient of the H 2 O elimination in acidic solution is (1.6±0.2)x10 6 s -1 , whereas the coefficient of the OH - elimination in alkaline solutions is 6-8 times higher. The kinetics of the phenoxyl radical formation was described by the two-exponential equation of the consecutive reactions: the first exponential is related to the pseudo-first-order addition, while the second to the elimination reaction. No considerable structure dependence was found in the rate coefficients, indicating that the methyl substitutent in these highly acidic or alkaline solutions influences neither the addition nor the elimination rate

Comparative study of polypyrrole films electrosynthesized in alkaline and acid solutions

International Nuclear Information System (INIS)

Lehr, I.L.; Quinzani, O.V.; Saidman, S.B.

2009-01-01

The influence of the pH of electropolymerization solutions on the properties of polypyrrole films has been studied using potentiodynamic techniques and faradaic impedance spectroscopy. Scanning electron microscopy (SEM), IR and Raman spectroscopies, thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) were also used for products characterization. Results indicate that, contrary to what happen with the polymer electrogenerated in acid solutions, the films prepared in alkaline media are stable and present good electrochemical activity in basic solutions. Possible explanations for the observed differences are discussed and it is proposed that the pH of electropolymerization medium directly affects chains organization. Electrosynthesis in solutions of increased basicity results in a more compact and closed polymer structure.

Evaluating Growth of Zeolites on Fly Ash in Hydro-Thermally Heated Low Alkaline Solution

Science.gov (United States)

Jha, Bhagwanjee; Singh, D. N.

2017-12-01

Fly ash has been well established materials for synthesis of zeolites, under hydrothermally heated aqueous NaOH solution. Efficacy of such technique is reported to be improved when high molarity of NaOH is used. Consequently, highly alkaline waste solution, as by-product, is generally disposed of in the surrounding, which may contaminate the environment. In this context, less alkaline NaOH solution may become a safer option, which has not been tried in the past as per the literature. With this in view, the present study demonstrates effectiveness of the 0.5 M NaOH solution and critically monitors transition on the fly ash after hydrothermal treatment. As an enhancement over previous researchers, such activation of the fly ash finally results in remarkable morphological and mineralogical growth on the bulk material (the residue), which comprises of new nano-sized crystals (the zeolites Na-P1 and natrolite), after 24 h of activation of the fly ash.

Strong alkalinization in the anterior midgut of larval yellow fever mosquitoes (Aedes aegypti): involvement of luminal Na+/K+-ATPase.

Science.gov (United States)

Onken, Horst; Patel, Malay; Javoroncov, Margarita; Izeirovski, Sejmir; Moffett, Stacia B; Moffett, David F

2009-03-01

Recently, Na(+)/K(+)-ATPase has been detected in the luminal membrane of the anterior midgut of larval yellow fever mosquitoes (Aedes aegypti) with immunohistochemical techniques. In this study, the possible involvement of this ATPase in strong alkalinization was investigated on the level of whole larvae, isolated and perfused midgut preparations and on the molecular level of the Na(+)/K(+)-ATPase protein. Ouabain (5 mM) did not inhibit the capability of intact larval mosquitoes to alkalinize their anterior midgut. Also in isolated and perfused midgut preparations the perfusion of the lumen with ouabain (5 mM) did not result in a significant change of the transepithelial voltage or the capacity of luminal alkalinization. Na(+)/K(+)-ATPase activity was completely abolished when KCl was substituted with choline chloride, suggesting that the enzyme cannot act as an ATP-driven Na(+)/H(+)-exchanger. Altogether the results of the present investigation indicate that apical Na(+)/K(+)-ATPase is not of direct importance for strong luminal alkalinization in the anterior midgut of larval yellow fever mosquitoes.

USING CERAMIC MEMBRANES TO RECYCLE TWO NONIONIC ALKALINE METAL-CLEANING SOLUTIONS

Science.gov (United States)

One ZrO2 ultrafilter (0.05 um pore size) and two a-Al2O3 microfilters (0.2 and 0.8 um) were used to remove one synthetic ester oil and two polyalphaolefin-based and two petroleum hydrocarbon-based oils and greases from two nonionic alkaline cleaning solutions (e.g., Turco 4215-NC...

MODELING AN ION EXCHANGE PROCESS FOR CESIUM REMOVAL FROM ALKALINE RADIOACTIVE WASTE SOLUTIONS

International Nuclear Information System (INIS)

Smith, F.; Hamm, Luther; Aleman, Sebastian; Michael, Johnston

2008-01-01

The performance of spherical Resorcinol-Formaldehyde ion-exchange resin for the removal of cesium from alkaline radioactive waste solutions has been investigated through computer modeling. Cesium adsorption isotherms were obtained by fitting experimental data using a thermodynamic framework. Results show that ion-exchange is an efficient method for cesium removal from highly alkaline radioactive waste solutions. On average, two 1300 liter columns operating in series are able to treat 690,000 liters of waste with an initial cesium concentration of 0.09 mM in 11 days achieving a decontamination factor of over 50,000. The study also tested the sensitivity of ion-exchange column performance to variations in flow rate, temperature and column dimensions. Modeling results can be used to optimize design of the ion exchange system

Impact of an Alkaline Solution on the Chemistry, Mineralogy, and Sorption Properties of a Typic Rhodudult Soil

Directory of Open Access Journals (Sweden)

Jaqueline Alves de Almeida Calábria

2017-11-01

Full Text Available Abstract The preferred option for disposal of short-lived low and intermediate level radioactive wastes is a near surface disposal facility in which soil is one of the barriers that avoid radionuclide migration outside the controlled area. For construction of that kind of facility, concrete is widely used, and its interaction with water induces its degradation, resulting in a high pH solution. The alkaline solution may affect the near-field environment of radioactive waste repositories, including the soil, promoting mineralogical alterations that result in significant changes in key properties of materials, compromising their performance as safety components. In this study, a sample of a Brazilian Typic Rhodudult soil, previously investigated concerning its performance for Cs sorption, was subjected to interaction with the alkaline solution for 24 h and for 7, 14, and 28 days in order to evaluate the impact on its chemical, mineralogical, and sorption properties. X-ray diffraction (XRD, energy dispersive X-ray spectroscopy (EDX, atomic absorption spectrometry (AAS, scanning electron microscopy (SEM, and electron microprobe analysis were performed before and after each alteration period. Results indicated dissolution of minerals, such as kaolinite and quartz, associated with incorporation of K and Ca from the alkaline solution, likely resulting in the formation of hydrated calcium silicate phases (CSH, which are expected to be worse sorbents for alkaline elements (e.g., Cs than the original minerals. The Kd values for Cs in the altered samples also decreased according to the alteration period, demonstrating that alkaline interaction effectively modifies the soil sorption properties for Cs.

Investigation of aluminum gate CMP in a novel alkaline solution

International Nuclear Information System (INIS)

Feng Cuiyue; Liu Yuling; Sun Ming; Zhang Wenqian; Zhang Jin; Wang Shuai

2016-01-01

Beyond 45 nm, due to the superior CMP performance requirements with the metal gate of aluminum in the advanced CMOS process, a novel alkaline slurry for an aluminum gate CMP with poly-amine alkali slurry is investigated. The aluminum gate CMP under alkaline conditions has two steps: stock polishing and fine polishing. A controllable removal rate, the uniformity of aluminum gate and low corrosion are the key challenges for the alkaline polishing slurry of the aluminum gate CMP. This work utilizes the complexation-soluble function of FA/O II and the preference adsorption mechanism of FA/O I nonionic surfactant to improve the uniformity of the surface chemistry function with the electrochemical corrosion research, such as OCP-TIME curves, Tafel curves and AC impedance. The result is that the stock polishing slurry (with SiO 2 abrasive) contains 1 wt.% H 2 O 2 ,0.5 wt.% FA/O II and 1.0 wt.% FA/O I nonionic surfactant. For a fine polishing process, 1.5 wt.% H 2 O 2 , 0.4 wt.% FA/O II and 2.0 wt.% FA/O I nonionic surfactant are added. The polishing experiments show that the removal rates are 3000 ± 50 Å/min and 1600 ± 60 Å/min, respectively. The surface roughnesses are 2.05 ± 0.128 nm and 1.59 ± 0.081 nm, respectively. A combination of the functions of FA/O II and FA/O I nonionic surfactant obtains a controllable removal rate and a better surface roughness in alkaline solution. (paper)

Volumetric determination of hydroxide, aluminate, and carbonate in alkaline solutions of nuclear waste

International Nuclear Information System (INIS)

Baumann, E.W.

1975-06-01

An integrated procedure was developed for determining OH - , Al(OH) 4 - , and CO 3 2- in alkaline nuclear waste. The free alkali, the hydroxide released when Al(OH) 3 is complexed with oxalate, and the precipitated BaCO 3 were determined by acidimetric titration. With a 50-μl sample, the relative standard deviations were 1 to 2 percent for nonradioactive test solutions and 2 to 5 percent for radioactive process solutions. (U.S.)

CRIEPI's research results (2006-2011) and clarified future issues on alteration behavior of bentonite barrier by alkaline solutions

International Nuclear Information System (INIS)

Yokoyama, Shingo; Nakamura, Kunihiko; Tanaka, Yukihisa; Hironaga, Michihiko

2013-01-01

In radioactive waste disposal facilities, bentonite barrier would be altered by alkaline solutions which arise by leaching of cementitious materials. Consequently suitable properties of the bentonite barrier would be degraded for a long time period. In CRIEPI, the investigation on the alteration of the bentonite under alkaline conditions was started in 2006, and several CRIEPI reports have been published. Specifically, we have investigated the kinetics of montmorillonite dissolution, the mineralogical alteration of compacted bentonite (with high- and low-dry density) and the change of permeability of the compacted bentonite (with high- and low-dry density) during alteration under the alkaline conditions. Furthermore, stability of saponite, which has similar physical properties to the bentonite, under the alkaline conditions was also examined. In this report, we show the outline of those research results, and lay out the clarified future issues extracted from our results. Ten clarified future issues were divided three categories as follows: 1) the estimation of the alteration behavior of the bentonite by alkaline solutions, 2) the elucidation of the mechanism of physical properties (e.g., permeability, swelling properties and mechanistic properties) change of the compacted bentonites during alteration, and 3) the development of the model building and simulation technology concerning the change in physical properties during alteration under alkaline conditions. (author)

Study of the Eosin-Y/PAMAM interactions in alkaline aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Arbeloa, Ernesto M., E-mail: earbeloa@exa.unrc.edu.ar [Universidad Nacional de Río Cuarto, Río Cuarto, 5800 Córdoba (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) (Argentina); Previtali, Carlos M. [Universidad Nacional de Río Cuarto, Río Cuarto, 5800 Córdoba (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) (Argentina); Bertolotti, Sonia G., E-mail: sbertolotti@exa.unrc.edu.ar [Universidad Nacional de Río Cuarto, Río Cuarto, 5800 Córdoba (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) (Argentina)

2016-04-15

The interactions between the xanthene dye Eosin-Y (Eos) and amino-terminated PAMAM dendrimers of low generations (G0–G3) were studied in alkaline water solution. The effect of concentration and generation of the dendrimer on the photophysics of Eos was evaluated by means of absorption and fluorescence spectroscopies. The observed spectral changes were ascribed to the association dye/dendrimer. From these data, the Eos/PAMAM binding constants (K{sub bind}) were determined, which strongly increased with the size of the dendrimer. Stationary fluorescence anisotropy and time-resolved single photon counting were also used to characterize the association process. The restriction in the rotational diffusion of the Eos increased as a function of the concentration and generation of PAMAM, as determined by anisotropy measurements. Biexponential fluorescence decays were obtained in the presence of G3, and the respective lifetimes were ascribed to free and bound Eos species. These results correlate with K{sub bind} values and suggest the formation of host/guest system with larger dendrimers. Therefore, this environmentally-friendly dye/dendrimer system would be appropriate for potential applications in fields such as drugs delivery and photopolymerization.

Study of the Eosin-Y/PAMAM interactions in alkaline aqueous solution

International Nuclear Information System (INIS)

Arbeloa, Ernesto M.; Previtali, Carlos M.; Bertolotti, Sonia G.

2016-01-01

The interactions between the xanthene dye Eosin-Y (Eos) and amino-terminated PAMAM dendrimers of low generations (G0–G3) were studied in alkaline water solution. The effect of concentration and generation of the dendrimer on the photophysics of Eos was evaluated by means of absorption and fluorescence spectroscopies. The observed spectral changes were ascribed to the association dye/dendrimer. From these data, the Eos/PAMAM binding constants (K bind ) were determined, which strongly increased with the size of the dendrimer. Stationary fluorescence anisotropy and time-resolved single photon counting were also used to characterize the association process. The restriction in the rotational diffusion of the Eos increased as a function of the concentration and generation of PAMAM, as determined by anisotropy measurements. Biexponential fluorescence decays were obtained in the presence of G3, and the respective lifetimes were ascribed to free and bound Eos species. These results correlate with K bind values and suggest the formation of host/guest system with larger dendrimers. Therefore, this environmentally-friendly dye/dendrimer system would be appropriate for potential applications in fields such as drugs delivery and photopolymerization.

Electrochemical Performance of Low-Carbon Steel in Alkaline Model Solutions Containing Hybrid Aggregates

NARCIS (Netherlands)

Koleva, D.A.; Hu, J.; De Wit, J.H.W.; Boshkov, N.; Radeva, T.; Milkova, V.; Van Breugel, K.

2010-01-01

This work reports on the electrochemical performance of low-carbon steel electrodes in model alkaline solutions in the presence of 4.9.10-4 g/l hybrid aggregates i.e. cement extract, containing PDADMAC (poly (diallyl, dimethyl ammonium chloride) / PAA (Poly (acrylic acid)/ PDADMAC over a CaO core.

Corrosion of silicon nitride in high temperature alkaline solutions

Energy Technology Data Exchange (ETDEWEB)

Qiu, Liyan, E-mail: liyan.qiu@cnl.ca; Guzonas, Dave A.; Qian, Jing

2016-08-01

The corrosion of silicon nitride (Si{sub 3}N{sub 4}) in alkaline solutions was studied at temperatures from 60 to 300 °C. Si{sub 3}N{sub 4} experienced significant corrosion above 100 °C. The release rates of silicon and nitrogen follow zero order reaction kinetics and increase with increasing temperature. The molar ratio of dissolved silicon and nitrogen species in the high temperature solutions is the same as that in the solid phase (congruent dissolution). The activation energy for silicon and nitrogen release rates is 75 kJ/mol which agrees well with that of silica dissolution. At 300 °C, the release of aluminum is observed and follows first order reaction kinetics while other minor constituents including Ti and Y are highly enriched on the corrosion films due to the low solubility of their oxides.

Defect structure of cubic solid solutions of alkaline earth and rare earth fluorides

NARCIS (Netherlands)

DenHartog, HW

1996-01-01

In this paper we will consider the disorder in some cubic solid solutions consisting of one of the alkaline earth fluorides and one of the rare earth fluorides. This is an attractive group of model materials, because these materials have a rather simple overall cubic structure. We will discuss the

Experimental and theoretical investigation on corrosion inhibition of AA5052 aluminium alloy by L-cysteine in alkaline solution

International Nuclear Information System (INIS)

Wang, Dapeng; Gao, Lixin; Zhang, Daquan; Yang, Dong; Wang, Hongxia; Lin, Tong

2016-01-01

The corrosion inhibition of L-cysteine on AA5052 aluminium alloy in 4 mol/L NaOH solution was investigated by hydrogen gas evolution experiment, polarisation curve, galvanostatic discharge, electrochemical impedance spectroscopy measurements and quantum chemical calculations. The adsorption of L-cysteine on aluminium alloy surface obeyed the amended Langmuir's adsorption isotherm. The polarisation curves indicated that L-cysteine acted as a cathodic inhibitor to inhibit cathodic reaction. The inhibition mechanism was dominated by the geometric covering effect. The galvanostatic discharge shows that the additives restrain the hydrogen evolution and increase the anodic utilization rate. Quantum chemical calculations indicated that L-cysteine molecules mainly interacted with on the carboxyl groups on the aluminium alloy surface. A strong hybridization occurred between the s-orbital and p-orbital of reactive sites in the L-cysteine molecule and the sp-orbital of Aluminium. - Highlights: • L-cysteine was used as corrosion inhibitor for Al alloy in alkaline solution. • Adsorption of L-cysteine on Al alloy surface obeyed the amended Langmuir's isotherm. • L-cysteine molecules interacted with the carboxyl groups on the Al alloy surface. • A strong orbital hybridization occurred between the reactive sites in L-cysteine and Al.

Electrodeposition of white copper-tin alloys from alkaline cyanide solutions

International Nuclear Information System (INIS)

Purwadaria, H.S.; Zainal Arifin Ahmad

2007-01-01

Electrodeposition of white copper-tin alloys (including with mir alloys) has been done onto planar mild steel substrates from alkaline cyanide solutions at 65 degree C. The chemical composition of the coating is influenced by plating bath composition and current density. White mir alloy can be produced from the test solution containing 10 g/l CuCN 2 ,45 g/l Na 2 SnO 3 , 25 g/l NaCN, and 12 g/l NaOH at current density about 5 mA/cm?2. The local compositions of the coating cross section were analyzed using EDX installed in a FESEM operated at an accelerating voltage of 20 kV. The phases formed during co-deposition process were identified using XRD at 25 mA current and 35 kV voltage. (Author)

Metal Oxide Decomposition In Hydrothermal Alkaline Sodium Phosphate Solutions

Energy Technology Data Exchange (ETDEWEB)

S.E. Ziemniak

2003-09-24

Alkaline hydrothermal solutions of sodium orthophosphate (2.15 < Na/P < 2.75) are shown to decompose transition metal oxides into two families of sodium-metal ion-(hydroxy)phosphate compounds. Equilibria for these reactions are quantified by determining phosphate concentration-temperature thresholds for decomposition of five oxides in the series: Ti(IV), Cr(III), Fe(III, II), Ni(II) and Zn(II). By application of a computational chemistry method General Utility Lattice Program (GULP), it is demonstrated that the unique non-whole-number Na/P molar ratio of sodium ferric hydroxyphosphate is a consequence of its open-cage structure in which the H{sup +} and excess Na{sup +} ions are located.

The stability of the strong gravity solution

International Nuclear Information System (INIS)

Baran, S.A.

1978-01-01

The perturbation of the classical solution to a strong gravity model given by Salam and Strathdee is investigated. Using the Hamiltonian formalism it is shown that this static and spherically symmetric solution is stable under the odd parity perturbations provided some parameters in the solution are suitably restricted

Eichrom's ABEC trademark resins: Alkaline radioactive waste treatment, radiopharmaceutical, and potential hydrometallurgical applications

International Nuclear Information System (INIS)

Bond, A.H.; Gula, M.J.; Chang, F.; Rogers, R.D.

1997-01-01

Eichrom's ABEC trademark resins selectivity extract certain anions from high ionic strength acidic, neutral, or strongly alkaline media, and solute stripping can be accomplished by eluting with water. ABEC resins are stable to pH extreme and radiolysis and operate in high ionic strength and/or alkaline solutions where anion-exchange is often ineffective. Potential applications of the ABEC materials include heavy metal and ReO 4 - separations in hydrometallurgy and purification of perrhenate iodide, and iodate in radiopharmaceutical production. Separation of 99m TcO 4 - from its 99 MoO 4 2- parent and stripping with water or physiological saline solution have been demonstrated for radiopharmaceutical applications. Removal of 99 TcO 4 - and 129 I - from alkaline tank wastes has also been successfully demonstrated. The authors will discuss the scale-up studies, process-scale testing, and market development of this new extraction material

A class of solutions for the strong gravity equations

International Nuclear Information System (INIS)

Salam, A.; Strathdee, J.

1976-12-01

We solve the Einstein equation for strong gravity in the limit that weak gravity is neglected. The class of solutions we find reduces to the Schwarzschild solution (with the weak gravity Newtonian constant replaced by a strong coupling parameter) in the limit M 2 →0 where M is the mass of the strong gravity spin-2 meson. These solutions may be of relevance for the problem of defining temperature in hadronic physics

Properties of altered soils by alkaline solution: contribution in the performance evaluation of repositories

International Nuclear Information System (INIS)

Calabria, Jaqueline Alves de Almeida

2015-01-01

evaluated samples (less than 20% after 10 days of equilibrium), being the best performance one, the nitosoil sample whose K_d values varied from 11.78 to 63.05 mL.g"-"1. In a subsequent step, the clay soil, was submitted to the alkaline solution interaction, in order to investigate possible alterations on the sorption properties and hydraulic conductivity of this soil. Using the sorption parameters, obtained from data fitted isotherms, the retardation factor, R, was estimated for the samples before and after the interaction. It was demonstrated that the alkaline alteration promotes damages to sorption properties of Cs, once the R became significantly smaller (about 1000 times) after the interaction. The hydraulic conductivity in turn increased slightly (3,91x10"-"8 cm.s"-"1 to 5,08 x 10"-"8 cm.s"-"1). It was concluded that these changes were due, mainly, to the dissolution of minerals present in the clay soil (kaolinite and quartz), associated with the incorporation of K and Ca from the alkaline solution, resulting, probably, in the formation of hydrated calcium silicate phases. Additionally, the effects of alkaline solution on the properties of a commercial bentonite were studied. Contrary to the clay soil, it was observed a gain in the sorption characteristics, with K_d (Cs) increasing from 760.05 mL.g"-"1to 1311.80 mL.g"-"1and Q_m_a_x from 36.32 mg.g"-"1to 52.13 mg.g"-"1, with the corresponding increase in the retardation coefficient, R. The dissolution of the clay minerals from the initial sample and the incorporation of Mg, K e Ca coming from the alkaline solution, generating smectite of different kinds, were considered as the main mineralogical changes responsible for the modifications in sorption parameters. The different behavior between the two evaluated samples, soil and bentonite, confirms that the nature and extension of changes observed, when mineral samples interact with alkaline solution, depend on the chemical/mineralogical composition of the solid material

Perturbation of an exact strong gravity solution

International Nuclear Information System (INIS)

Baran, S.A.

1982-10-01

Perturbations of an exact strong gravity solution are investigated. It is shown, by using the new multipole expansions previously presented, that this exact and static spherically symmetric solution is stable under odd parity perturbations. (author)

Effectiveness of the squeezing out and final squeezing out of petroleum of an increased viscosity by alkaline solutions

Energy Technology Data Exchange (ETDEWEB)

Begnazarov, T.

1979-01-01

The remaining petroleum in the flooded zone is determined by the ratio of viscosity forces to the forces of the surface tension, which are expressed by the coefficient Ka. With this, for each kind of porous medium, there exists a natural cricial value Ka. For the purpose of studying the effect of the given parameters on the value of the remaining petroleum, experiments were carried out on artificial specimens. In the tests, using petroleum of the Mishkin deposit, the surface tension on the boundary of the petroleum with the distilled water and alkaline solutions were respectively equal to 37.1 and 1.33 dynes per centimeter. The experiments showed, that the squeezing out of the petroleum with water or alkaline solutions leads to similar results. This means, that the composite parameter Ka does not affect the value of the remaining petroleum saturation. The effectiveness of the final squeezing out of the petroleum of increased viscosity was also studied. These experiments were carried out in two variations of the injection of the squeezed out agent: in the first variation, the petroleum was squeezed out with water in the first stage, and in the second stage it was squeezed out by an alkaline solution, and in the subsequent stages, a change in the squeezing out agent took place. By finishing the first stage, the attained values of the coefficients of the squeezing out were practically similar (0.72). In the second stage, the final squeezing out of the petroleum with a solution of alkaline, provided a major effect.

Characterization of Laboratory Prepared Concrete Pastes Exposed to High Alkaline and High Sodium Salt Solutions

Energy Technology Data Exchange (ETDEWEB)

Langton, C. A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2016-06-30

The objective of this study was to identify potential chemical degradation mechanisms for the Saltstone Disposal Unit (SDU) concretes, which over the performance life of the structures may be exposed to highly alkaline sodium salt solutions containing sulfate, hydroxide, and other potentially corrosive chemicals in salt solution and saltstone flush water, drain water, leachate and / or pore solution. The samples analyzed in this study were cement pastes prepared in the SIMCO Technologies, Inc. concrete laboratory. They were based on the paste fractions of the concretes used to construct the Saltstone Disposal Units (SDUs). SDU 1 and 4 concrete pastes were represented by the PV1 test specimens. The paste in the SDU 2, 3, 5, and 6 concrete was represented by the PV2 test specimens. SIMCO Technologies, Inc. selected the chemicals and proportions in the aggressive solutions to approximate proportions in the saltstone pore solution [2, 3, 5, and 6]. These test specimens were cured for 56 days in curing chamber before being immersed in aggressive solutions. After exposure, the samples were frozen to prevent additional chemical transport and reaction. Selected archived (retrieved from the freezer) samples were sent to the Savannah River National Laboratory (SRNL) for additional characterization using x-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive x-ray (EDX) spectroscopy. Characterization results are summarized in this report. In addition, a correlation between the oxide composition of the pastes and their chemical durability in the alkaline salt solutions is provided.

Analytical solution of strongly nonlinear Duffing oscillators

OpenAIRE

El-Naggar, A.M.; Ismail, G.M.

2016-01-01

In this paper, a new perturbation technique is employed to solve strongly nonlinear Duffing oscillators, in which a new parameter α=α(ε)α=α(ε) is defined such that the value of α is always small regardless of the magnitude of the original parameter εε. Therefore, the strongly nonlinear Duffing oscillators with large parameter ε are transformed into a small parameter system with respect to αα. Approximate solution obtained by the present method is compared with the solution of energy balance m...

Electro-oxidation of methanol on copper in alkaline solution

International Nuclear Information System (INIS)

Heli, H.; Jafarian, M.; Mahjani, M.G.; Gobal, F.

2004-01-01

The electro-oxidation of methanol on copper in alkaline solutions has been studied by the methods of cyclic voltammetry, quasi-steady state polarization and chronoamperometry. It has been found that in the course of an anodic potential sweep the electro-oxidation of methanol follows the formation of Cu III and is catalysed by this species through a mediated electron transfer mechanism. The reaction also continues in the early stages of the reversed cycle until it is stopped by the prohibitively negative potentials. The process is diffusion controlled and the current-time responses follow Cottrellian behavior. The rate constants, turnover frequency, anodic transfer coefficient and the apparent activation energy of the electro-oxidation reaction are reported

A study on the mechanism of stress corrosion cracking of duplex stainless steels in hot alkaline-sulfide solution

Science.gov (United States)

Chasse, Kevin Robert

Duplex stainless steels (DSS) generally have superior strength and corrosion resistance as compared to most standard austenitic and ferritic stainless grades owing to a balanced microstructure of austenite and ferrite. As a result of having favorable properties, DSS have been selected for the construction of equipment in pulp and paper, chemical processing, nuclear, oil and gas as well as other industries. The use of DSS has been restricted in some cases because of stress corrosion cracking (SCC), which can initiate and grow in either the ferrite or austenite phase depending on the environment. Thorough understanding of SCC mechanisms of DSS in chloride- and hydrogen sulfide-containing solutions has been useful for material selection in many environments. However, understanding of SCC mechanisms of DSS in sulfide-containing caustic solutions is limited, which has restricted the capacity to optimize process and equipment design in pulp and paper environments. Process environments may contain different concentrations of hydroxide, sulfide, and chloride, altering corrosion and SCC susceptibility of each phase. Crack initiation and growth behavior will also change depending on the relative phase distribution and properties of austenite and ferrite. The role of microstructure and environment on the SCC of standard grade UNS S32205 and lean grade UNS S32101 in hot alkaline-sulfide solution were evaluated in this work using electrochemical, film characterization, mechanical testing, X-ray diffraction, and microscopy techniques. Microstructural aspects, which included residual stress state, phase distribution, phase ratio, and microhardness, were related to the propensity for SCC crack initiation in different simulated alkaline pulping liquors at 170 °C. Other grades of DSS and reference austenitic and superferritic grades of stainless steel were studied using exposure coupons for comparison to understand compositional effects and individual phase susceptibility

Alteration behavior of bentonite barrier of radioactive waste disposal by alkaline solutions. Part 2. Effect of type of alkaline solution on permeability of compacted bentonite-sand mixture

International Nuclear Information System (INIS)

Yokoyama, Shingo; Nakamura, Kunihiko; Tanaka, Yukihisa; Hironaga, Michihiko

2011-01-01

Permeability tests were carried out using compacted bentonite-sand mixture with initial dry density of 1.55 Mg/m 3 and alkaline solutions at 50degC for about two years to estimate the alteration behavior and the change in the permeability. Bentonite-sand mixtures which contain bentonites of 15wt% were made using Na-bentonite or Ca-exchanged bentonite. 0.3M-NaOH solution with pH 13.3 and 5mM-Ca(OH) 2 solution with pH 12.0 were used to the permeability tests of Na-bentonite-sand mixture and of Ca-exchanged bentonite-sand mixture, respectively. In the case of the permeability test conducted using NaOH solution, montmorillonite and other associated minerals were dissolved, and consequently, the dry density and effective montmorillonite density of Na-bentonite-sand mixture were decreased. Furthermore, the mineralogical feature of montmorillonite was changed (i.e. beidellitization and an increase in the layer charge). The permeability of Na-bentonite-sand mixture was increased 5.6 times by the end of permeability test as a result of above alteration. In the case of the permeability test conducted using Ca(OH) 2 solution, montmorillonite and other associated minerals were dissolved, and calcium silicate hydrate (C-S-H) was precipitated. Consequently, the dry density of Ca-exchanged bentonite-sand mixture was increased, while the effective montmorillonite density was decreased. The mineralogical feature of montmorillonite was changed (i.e. beidellitization and an increase in the layer charge). The permeability of Ca-exchange bentonite-sand mixture was decreased by more than two orders of magnitude due to fill the pore of Ca-exchange bentonite-sand mixture by the precipitation of C-S-H. From above results, the type of alkaline solution affects the mineralogical alteration behavior of the compacted bentonite-sand mixture, and consequently, affects the changing trend of permeability. In conclusion, it is important not only to consider the dissolution of montmorillonite, but

Analytical solution of strongly nonlinear Duffing oscillators

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A.M. El-Naggar

2016-06-01

Full Text Available In this paper, a new perturbation technique is employed to solve strongly nonlinear Duffing oscillators, in which a new parameter α=α(ε is defined such that the value of α is always small regardless of the magnitude of the original parameter ε. Therefore, the strongly nonlinear Duffing oscillators with large parameter ε are transformed into a small parameter system with respect to α. Approximate solution obtained by the present method is compared with the solution of energy balance method, homotopy perturbation method, global error minimization method and lastly numerical solution. We observe from the results that this method is very simple, easy to apply, and gives a very good accuracy not only for small parameter εbut also for large values of ε.

Experimental and theoretical investigation on corrosion inhibition of AA5052 aluminium alloy by L-cysteine in alkaline solution

Energy Technology Data Exchange (ETDEWEB)

Wang, Dapeng; Gao, Lixin [School of Environmental and Chemical Engineering, Shanghai University of Electric Power, Shanghai 200090 (China); Zhang, Daquan, E-mail: zhangdaquan@shiep.edu.cn [School of Environmental and Chemical Engineering, Shanghai University of Electric Power, Shanghai 200090 (China); Yang, Dong [School of Environmental and Chemical Engineering, Shanghai University of Electric Power, Shanghai 200090 (China); Wang, Hongxia; Lin, Tong [Institute for Frontier Materials, Deakin University, Geelong, VIC 3216 (Australia)

2016-02-01

The corrosion inhibition of L-cysteine on AA5052 aluminium alloy in 4 mol/L NaOH solution was investigated by hydrogen gas evolution experiment, polarisation curve, galvanostatic discharge, electrochemical impedance spectroscopy measurements and quantum chemical calculations. The adsorption of L-cysteine on aluminium alloy surface obeyed the amended Langmuir's adsorption isotherm. The polarisation curves indicated that L-cysteine acted as a cathodic inhibitor to inhibit cathodic reaction. The inhibition mechanism was dominated by the geometric covering effect. The galvanostatic discharge shows that the additives restrain the hydrogen evolution and increase the anodic utilization rate. Quantum chemical calculations indicated that L-cysteine molecules mainly interacted with on the carboxyl groups on the aluminium alloy surface. A strong hybridization occurred between the s-orbital and p-orbital of reactive sites in the L-cysteine molecule and the sp-orbital of Aluminium. - Highlights: • L-cysteine was used as corrosion inhibitor for Al alloy in alkaline solution. • Adsorption of L-cysteine on Al alloy surface obeyed the amended Langmuir's isotherm. • L-cysteine molecules interacted with the carboxyl groups on the Al alloy surface. • A strong orbital hybridization occurred between the reactive sites in L-cysteine and Al.

Perturbation Solutions of the Quintic Duffing Equation with Strong Nonlinearities

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Mehmet Pakdemirli

Full Text Available The quintic Duffing equation with strong nonlinearities is considered. Perturbation solutions are constructed using two different techniques: The classical multiple scales method (MS and the newly developed multiple scales Lindstedt Poincare method (MSLP. The validity criteria for admissible solutions are derived. Both approximate solutions are contrasted with the numerical solutions. It is found that MSLP provides compatible solution with the numerical solution for strong nonlinearities whereas MS solution fail to produce physically acceptable solution for large perturbation parameters.

Investigation on the co-precipitation of transuranium elements from alkaline solutions by the method of appearing reagents

International Nuclear Information System (INIS)

Krot, N.; Shilov, V.; Bessonov, A.; Budantseva, N.; Charushnikova, I.; Perminov, V.; Astafurova, L.

1996-06-01

Highly alkaline radioactive waste solutions originating from production of plutonium for military purposes are stored in underground tanks at the U.S. Department of Energy Hanford Site. The purification of alkaline solutions from neptunium and plutonium is important in the treatment and disposal of these wastes. This report describes scoping tests with sodium hydroxide solutions, where precipitation techniques were investigated to perform the separation. Hydroxides of iron (III), manganese (II), cobalt (II, III), and chromium (III); manganese (IV) oxide, and sodium uranate were investigated as carriers. The report describes the optimum conditions that were identified to precipitate these carriers homogeneously throughout the solution by reductive, hydrolytic, or catalytic decomposition of alkali-soluble precursor compounds by a technique called the Method of Appearing Reagents. The coprecipitation of pentavalent and hexavalent neptunium and plutonium was investigated for the candidate agents under optimum conditions and is described in this report along with the following results. Plutonium coprecipitated well with all tested materials except manganese (IV) oxide. Neptunium only coprecipitated well with uranate. The report presents a hypothesis to explain these behaviors. Further tests with more complex solution matrices must be performed

Investigation on the co-precipitation of transuranium elements from alkaline solutions by the method of appearing reagents

Energy Technology Data Exchange (ETDEWEB)

Krot, N.; Shilov, V.; Bessonov, A.; Budantseva, N.; Charushnikova, I.; Perminov, V.; Astafurova, L. [Russian Academy of Science (Russian Federation). Inst. of Physical Chemistry

1996-06-06

Highly alkaline radioactive waste solutions originating from production of plutonium for military purposes are stored in underground tanks at the U.S. Department of Energy Hanford Site. The purification of alkaline solutions from neptunium and plutonium is important in the treatment and disposal of these wastes. This report describes scoping tests with sodium hydroxide solutions, where precipitation techniques were investigated to perform the separation. Hydroxides of iron (III), manganese (II), cobalt (II, III), and chromium (III); manganese (IV) oxide, and sodium uranate were investigated as carriers. The report describes the optimum conditions that were identified to precipitate these carriers homogeneously throughout the solution by reductive, hydrolytic, or catalytic decomposition of alkali-soluble precursor compounds by a technique called the Method of Appearing Reagents. The coprecipitation of pentavalent and hexavalent neptunium and plutonium was investigated for the candidate agents under optimum conditions and is described in this report along with the following results. Plutonium coprecipitated well with all tested materials except manganese (IV) oxide. Neptunium only coprecipitated well with uranate. The report presents a hypothesis to explain these behaviors. Further tests with more complex solution matrices must be performed.

Exact solutions of strong gravity in generalized metrics

International Nuclear Information System (INIS)

Hojman, R.; Smailagic, A.

1981-05-01

We consider classical solutions for the strong gravity theory of Salam and Strathdee in a wider class of metrics with positive, zero and negative curvature. It turns out that such solutions exist and their relevance for quark confinement is explored. Only metrics with positive curvature (spherical symmetry) give a confining potential in a simple picture of the scalar hadron. This supports the idea of describing the hadron as a closed microuniverse of the strong metric. (author)

Early containment of high-alkaline solution simulating low-level radioactive waste stream in clay-bearing blended cement

International Nuclear Information System (INIS)

Kruger, A.A.; Olson, R.A.; Tennis, P.D.

1995-04-01

Portland cement blended with fly ash and attapulgite clay was mixed with high-alkaline solution simulating low-level radioactive waste stream at a one-to-one weight ratio. Mixtures were adiabatically and isothermally cured at various temperatures and analyzed for phase composition, total alkalinity, pore solution chemistry, and transport properties as measured by impedance spectroscopy. Total alkalinity is characterized by two main drops. The early one corresponds to a rapid removal of phosphorous, aluminum, sodium, and to a lesser extent potassium solution. The second drop from about 10 h to 3 days is mainly associated with the removal of aluminum, silicon, and sodium. Thereafter, the total alkalinity continues descending, but at a lower rate. All pastes display a rapid flow loss that is attributed to an early precipitation of hydrated products. Hemicarbonate appears as early as one hour after mixing and is probably followed by apatite precipitation. However, the former is unstable and decomposes at a rate that is inversely related to the curing temperature. At high temperatures, zeolite appears at about 10 h after mixing. At 30 days, the stabilized crystalline composition Includes zeolite, apatite and other minor amounts of CaCO 3 , quartz, and monosulfate Impedance spectra conform with the chemical and mineralogical data. The normalized conductivity of the pastes shows an early drop, which is followed by a main decrease from about 12 h to three days. At three days, the permeability of the cement-based waste as calculated by Katz-Thompson equation is over three orders of magnitude lower than that of ordinary portland cement paste. However, a further decrease in the calculated permeability is questionable. Chemical stabilization is favorable through incorporation of waste species into apatite and zeolite

Iterative solutions of nonlinear equations with strongly accretive or strongly pseudocontractive maps

International Nuclear Information System (INIS)

Chidume, C.E.

1994-03-01

Let E be a real q-uniformly smooth Banach space. Suppose T is a strongly pseudo-contractive map with open domain D(T) in E. Suppose further that T has a fixed point in D(T). Under various continuity assumptions on T it is proved that each of the Mann iteration process or the Ishikawa iteration method converges strongly to the unique fixed point of T. Related results deal with iterative solutions of nonlinear operator equations involving strongly accretive maps. Explicit error estimates are also provided. (author). 38 refs

Removal of radioruthenium from alkaline intermediate level radioactive waste solution : a laboratory investigation

International Nuclear Information System (INIS)

Samanta, S.K.; Theyyunni, T.K.

1994-01-01

Various methods were investigated in the laboratory for the removal of radioruthenium from alkaline intermediate level radioactive waste solutions of reprocessing plant origin. The methods included batch equilibration with different ion exchangers and sorbents, column testing and chemical precipitation. A column method using zinc-activated carbon mixture and a chemical precipitation method using ferrous salt along with sodium sulphite were found to be promising for plant scale application. (author). 10 refs., 3 figs., 7 tabs

Effect of alkaline earth metal and magnesium cations on cadmium extraction from chloride solutions by tributyl phosphate

International Nuclear Information System (INIS)

Prokuev, V.A.; Belousov, E.A.

1985-01-01

At 298 K thermodynamic constants of cadmium (2) extraction from chloride solutions of magnesium, calcium, strontium and barium by tributyl phosphate are calculated. It is established, that logarithm of the thermodynamic extraction constant is in a linear dependence from the change in the cation hydration enthalpy in agqueous solution. It is shown, that activity coefficient of neutral complex CdVCl 2 differs from one, and it is the higher the more stable the complex is in alkaline earth metal chloride solutions

Arsenic removal from alkaline leaching solution using Fe (III) precipitation.

Science.gov (United States)

Wang, Yongliang; Lv, Cuicui; Xiao, Li; Fu, Guoyan; Liu, Ya; Ye, Shufeng; Chen, Yunfa

2018-02-02

The alkaline leaching solution from arsenic-containing gold concentrate contains a large amount of arsenate ions, which should be removed because it is harmful to the production process and to the environment. In this study, conventional Fe (III) precipitation was used to remove arsenic from the leaching solution. The precipitation reaction was carried out at the normal temperature, and the effects of pH value and Fe/As ratio on the arsenic removal were investigated. The results show that the removal rate of arsenic is distinctive at different pH values, and the effect is best within the pH range of 5.25-5.96. The removal rate can be further increased by increasing the ratio of Fe/As. When the pH = 5.25-5.96 and Fe/As > 1.8, the arsenic in the solution can be reduced to below 5 mg/L. However, the crystallinity of ferric arsenate is poor, and the particle size is small, most of which is about 1 μm. The leaching toxicity test shows the leaching toxicity of precipitates gradually decreased by the increase of Fe/As. The precipitates can be stored safely as the ratio of Fe/As exceeded 2.5.

Coprecipitation of trace amounts of 137Cs and 85Sr with [Na(18-Crown-6]BPh4 from neutral and alkaline solutions

International Nuclear Information System (INIS)

Kulyukhin, S.A.; Konovalova, N.A.; Rumer, I.A.; Kamenskaya, A.N.; Mikheev, N.B.

2005-01-01

Coprecipitation of 137 Cs and 85 Sr with [Na(18-crown-6]BPh 4 solid phase from aqueous, aqueous-ethanolic, and alkaline solutions is studied. 137 C s and 85 Sr co-crystallize with [Na(18-crown-6]BPh 4 from aqueous and aqueous-ethanolic solutions. The cocrystallization coefficients D of 137 Cs and 85 Sr from aqueous solutions are 2.6 ± 0.5 and 3.3 ± 0.3, respectively. For aqueous-ethanolic solutions, the corresponding values are 4.4 ± 0.5 and 3.4 ± 0.4. In the alkaline solutions (0.1 and 1 M NaOH), 54-74% of 137 Cs and 37-51% of 85 Sr pass into the [Na(18-crown-6)]BPh 4 solid phase, depending on the crown ether concentration in the system [ru

Alkaline earth metals

International Nuclear Information System (INIS)

Brown, Paul L.; Ekberg, Christian

2016-01-01

The beryllium ion has a relatively small ionic radius. As a consequence of this small size, its hydrolysis reactions begin to occur at a relatively low pH. To determine the stability and solubility constants, however, the Gibbs energy of the beryllium ion is required. In aqueous solution calcium, like the other alkaline earth metals, only exists as a divalent cation. The size of the alkaline earth cations increases with increasing atomic number, and the calcium ion is bigger than the magnesium ion. The hydrolysis of barium(II) is weaker than that of strontium(II) and also occurs in quite alkaline pH solutions, and similarly, only the species barium hydroxide has been detected. There is only a single experimental study on the hydrolysis of radium. As with the stability constant trend, it would be expected that the enthalpy of radium would be lower than that of barium due to the larger ionic radius.

Chemiluminescence of carbon dots induced by diperiodato-nicklate (IV) in alkaline solution and its application to a quenchometric flow-injection assays of paracetamole, L-cysteine and glutathione

International Nuclear Information System (INIS)

Dong, Yajuan; Su, Ming; Chen, Peiyun; Sun, Hanwen

2015-01-01

Aqueous solutions of carbon dots (C-dots) were prepared by microwave-assisted thermal carbonization of poly(ethylene glycol). They were investigated by transmission electron microscopy, absorption and fluorescence spectra. It is shown that diperiodato-nicklate(IV), a strong oxidant, induces the chemiluminescence (CL) of C-dots in strongly alkaline solution without use of an additional reagent. A mechanism for this reaction is suggested. It is also found that the CL of the system is quenched by paracetamole, L-cysteine and glutathione. Under the optimized conditions, the calibration plot is linear with a correlation coefficient (r) of >0.995. The limits of detection are 90, 8, and 60 µg L -1 for paracetamole, L-cysteine, and glutathione, respectively. Spiked urine and serum samples were analyzed and gave recoveries in the range from 84.38 to 116.0 %, with an RSD of 1.2–2.7 %. (author)

High-Strength / High Alkaline Resistant Fe-Phosphate Glass Fibers as Concrete Reinforcement

Energy Technology Data Exchange (ETDEWEB)

Mariano Velez

2008-03-31

Calcium-iron-phosphate glasses were developed whose chemical durabilities in alkaline solutions (pH 13) were comparable or superior to those of commercial alkaline-resistant (AR) silica-based glasses. However, the tensile strength of Ca-Fe-phosphate fibers, after being exposed to alkaline environments, including wet Portland cement pastes, is lower than that of current AR silicate fibers. Another series of Ca-Fe-phosphate glasses were developed with excellent chemical durability in strong acidic solutions (H2SO4, HF), indicating potential applications where silica-based fibers degrade very quickly, including E-glass. The new Ca-Fe-phosphate glasses can be melted and processed 300 to 500°C lower than silica-based glasses. This offers the possibility of manufacturing glass fibers with lower energy costs by 40-60% and the potential to reduce manufacturing waste and lower gas emissions. It was found that Ca-Fe-phosphate melts can be continuously pulled into fibers depending on the slope of the viscosity-temperature curve and with viscosity ~100 poise, using multi-hole Pt/Rh bushings.

Zinc electrodeposition from alkaline zincate solution by pulsating overpotentials

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MILOS V. SIMICIC

2000-09-01

Full Text Available It is well known that smooth zinc deposits cannot be obtained from alkaline zincate using constant overpotential and current rate. During prolonged metal deposition, spongy and dendritic deposits are formed. It has been shown that the deposits are less agglomerated in the case of square-wave pulsating overpotentials regime than the ones obtained in case of constant overpotential regime. This is explained in a semiquantitative way by two phenomena: selective anodic dissolution during overpotentials “off” period and decreasing diffusion control. These effects is more pronounced at higher pause-to-pulse ratio. Increasing the pause-to-pulse ratio causes a reduction of the ratio between diffusion and activation overpotential, resulting in a more compact deposit. Confirmation of the proposed semiquantitative mathematical model was obtained by zinc electrodeposition onto a copper wire from a 0.1 M zincate solution in 1.0 M KOH at room temperature.

Durability of template-free Fe-N-C foams for electrochemical oxygen reduction in alkaline solution

Science.gov (United States)

Mufundirwa, Albert; Harrington, George F.; Smid, Břetislav; Cunning, Benjamin V.; Sasaki, Kazunari; Lyth, Stephen M.

2018-01-01

Due to the high cost and limited availability of platinum, the development of non-platinum-group metals (non-PGM) catalysts is of paramount importance. A promising alternative to Pt are Fe-N-C-based materials. Here we present the synthesis, characterization and electrochemistry of a template-free nitrogen-doped carbon foam, impregnated with iron. This low-cost and gram-scale method results in materials with micron-scale pore size and large surface area (1600 m2g-1). When applied as an oxygen reduction reaction (ORR) electrocatalyst in alkaline solution, the Fe-N-C foams display extremely high initial activity, slightly out-performing commercially available non-PGM catalysts (NCP-2000, Pajarito Powder). The load-cycle durability in alkaline solution is investigated, and the performance steadily degrades over 60,000 potential cycles, whilst the commercial catalyst is remarkably stable. The post-operation catalyst microstructure is elucidated by transmission electron microscopy (TEM), to provide insight into the degradation processes. The resulting images suggest that potential cycling leads to leaching of atomically dispersed Fe-N2/4 sites in all the catalysts, whereas encapsulated iron nanoparticles are protected.

Influence of ionic strength and OH(-) ion concentration on the Cu(II) complex formation with EDTA in alkaline solutions.

Science.gov (United States)

Norkus, E; Vaskelis, A; Zakaite, I

1996-03-01

D.c. polarographic data show that the complex formation of copper ions with EDTA depends markedly on the ionic strength of the solution at pH 8-10. This is primarily associated with the dependence of the fourth deprotonization constant of EDTA on the solution ionic strength: when it increases from 0.4 to 3.4, the pK(a4) value decreases from 9.5 to 8.2. According to polarographic and spectrophotometric data the degree of Cu(II) complexation increases at pH>10 due to transformation of the complex CuY(2-) to the more stable CuY(OH)(3-) (Y(4-), a fully deprotonized anion of EDTA), but it decreases with increase in alkalinity in a highly alkaline solution (pH>13.5). The latter result could be explained by the decrease in the EDTA anion activity. The calculated values of the activity coefficient are lower than 0.05 at pH>14.

Cyclohexanone solvent extraction of 99TcO4 from alkaline nuclear waste solutions

International Nuclear Information System (INIS)

Schulz, W.W.

1980-01-01

Although the 99 Tc cyclohexanone solvent extraction process is still in the bench-scale development stage, the process appears well suited for engineering-scale removal of 99 Tc from alkaline Hanford waste solutions. The most pressing process development need is to resolve the phase disengaging problems encountered during water stripping operations. Stripping tests in pulse columns and/or centrifugal contactors are particularly needed to determine the magnitude of the phase disengaging problem in engineering-scale equipment and to find suitable remedies. 5 figures, 7 tables

Effect of Additional Sulfide and Thiosulfate on Corrosion of Q235 Carbon Steel in Alkaline Solutions

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Bian Li Quan

2016-01-01

Full Text Available This paper investigated the effect of additional sulfide and thiosulfate on Q235 carbon steel corrosion in alkaline solutions. Weight loss method, scanning electron microscopy (SEM equipped with EDS, X-ray photoelectron spectroscopy (XPS, and electrochemical measurements were used in this study to show the corrosion behavior and electrochemistry of Q235 carbon steel. Results indicate that the synergistic corrosion rate of Q235 carbon steel in alkaline solution containing sulfide and thiosulfate is larger than that of sulfide and thiosulfate alone, which could be due to redox reaction of sulfide and thiosulfate. The surface cracks and pitting characteristics of the specimens after corrosion were carefully examined and the corrosion products film is flake grains and defective. The main corrosion products of specimen induced by S2− and S2O32- are FeS, FeS2, Fe3O4, and FeOOH. The present study shows that the corrosion mechanism of S2− and S2O32- is different for the corrosion of Q235 carbon steel.

THE KINETICS OF SAPONIFICATION OF IODOACETIC ACID BY SODIUM HYDROXIDE AND BY CERTAIN ALKALINE BUFFER SOLUTIONS.

Science.gov (United States)

Brdicka, R

1936-07-20

1. The rate of the saponification of iodoacetic acid in sodium hydroxide and alkaline buffer solutions yielding glycollic acid was measured by means of Heyrovský's polarographic method. 2. From the bimolecular velocity constants, increasing with the ionic strength of the solution, the Brönsted factor, F, which characterizes the primary salt effect, was calculated. 3. In the borate buffer solutions the monomolecular constants of the saponification were determined which, at values above the pH of neutralization of boric acid, show a proportionality to the concentration of hydroxyl anions. Below the pH of neutralization of boric acid, they are proportional to the concentration of borate anions.

Iterative solution of nonlinear equations with strongly accretive operators

International Nuclear Information System (INIS)

Chidume, C.E.

1991-10-01

Let E be a real Banach space with a uniformly convex dual, and let K be a nonempty closed convex and bounded subset of E. Suppose T:K→K is a strongly accretive map such that for each f is an element of K the equation Tx=f has a solution in K. It is proved that each of the two well known fixed point iteration methods (the Mann and Ishikawa iteration methods) converges strongly to a solution of the equation Tx=f. Furthermore, our method shows that such a solution is necessarily unique. Explicit error estimates are given. Our results resolve in the affirmative two open problems (J. Math. Anal. Appl. Vol 151(2) (1990), p. 460) and generalize important known results. (author). 32 refs

Coupling the Alkaline-Surfactant-Polymer Technology and The Gelation Technology to Maximize Oil Production

Energy Technology Data Exchange (ETDEWEB)

Malcolm Pitts; Jie Qi; Dan Wilson; Phil Dowling; David Stewart; Bill Jones

2005-12-01

Gelation technologies have been developed to provide more efficient vertical sweep efficiencies for flooding naturally fractured oil reservoirs or reservoirs with different sand lenses with high permeability contrast. The field proven alkaline-surfactant-polymer technology economically recovers 15% to 25% OOIP more crude oil than waterflooding from swept pore space of an oil reservoir. However, alkaline-surfactant-polymer technology is not amenable to naturally fractured reservoirs or reservoirs with high permeability contrast zones because much of injected solution bypasses target pore space containing oil. This work investigates whether combining these two technologies could broaden applicability of alkaline-surfactant-polymer flooding into these reservoirs. Fluid-fluid interaction with different gel chemical compositions and alkaline-surfactant-polymer solution with pH values ranging from 9.2 to 12.9 have been tested. Aluminum-polyacrylamide gels are not stable to alkaline-surfactant-polymer solutions at any pH. Chromium-polyacrylamide gels with polymer to chromium ion ratios of 25 or greater were stable to alkaline-surfactant-polymer solutions if solution pH was 10.6 or less. When the polymer to chromium ion was 15 or less, chromium-polyacrylamide gels were stable to alkaline-surfactant-polymer solutions with pH values up to 12.9. Chromium-xanthan gum gels were stable to alkaline-surfactant-polymer solutions with pH values of 12.9 at the polymer to chromium ion ratios tested. Silicate-polyacrylamide, resorcinol-formaldehyde, and sulfomethylated resorcinol-formaldehyde gels were also stable to alkaline-surfactant-polymer solutions with pH values ranging from 9.2 to 12.9. Iron-polyacrylamide gels were immediately destroyed when contacted with any of the alkaline-surfactant-polymer solutions with pH values ranging from 9.2 to 12.9. Gel solutions under dynamic conditions of linear corefloods showed similar stability to alkaline-surfactant-polymer solutions as in

Coupling the Alkaline-Surfactant-Polymer Technology and the Gelation Technology to Maximize Oil Production

Energy Technology Data Exchange (ETDEWEB)

Malcolm Pitts; Jie Qi; Dan Wilson; Phil Dowling; David Stewart; Bill Jones

2005-12-01

Gelation technologies have been developed to provide more efficient vertical sweep efficiencies for flooding naturally fractured oil reservoirs or reservoirs with different sand lenses with high permeability contrast. The field proven alkaline-surfactant-polymer technology economically recovers 15% to 25% OOIP more crude oil than waterflooding froin swept pore space of an oil reservoir. However, alkaline-surfactant-polymer technology is not amenable to naturally fractured reservoirs or reservoirs with high permeability contrast zones because much of injected solution bypasses target pore space containing oil. This work investigates whether combining these two technologies could broaden applicability of alkaline-surfactant-polymer flooding into these reservoirs. Fluid-fluid interaction with different gel chemical compositions and alkaline-surfactant-polymer solution with pH values ranging from 9.2 to 12.9 have been tested. Aluminum-polyacrylamide gels are not stable to alkaline-surfactant-polymer solutions at any pH. Chromium-polyacrylamide gels with polymer to chromium ion ratios of 25 or greater were stable to alkaline-surfactant-polymer solutions if solution pH was 10.6 or less. When the polymer to chromium ion was 15 or less, chromium-polyacrylamide gels were stable to alkaline-surfactant-polymer solutions with pH values up to 12.9. Chromium-xanthan gum gels were stable to alkaline-surfactant-polymer solutions with pH values of 12.9 at the polymer to chromium ion ratios tested. Silicate-polyacrylamide, resorcinol-formaldehyde, and sulfomethylated resorcinol-formaldehyde gels were also stable to alkaline-surfactant-polymer solutions with pH values ranging from 9.2 to 12.9. Iron-polyacrylamide gels were immediately destroyed when contacted with any of the alkaline-surfactant-polymer solutions with pH values ranging from 9.2 to 12.9. Gel solutions under dynamic conditions of linear corefloods showed similar stability to alkaline-surfactant-polymer solutions as in

Roughness comparison of heat cured type of acrylic resin in disinfectant solution immersion (Immersion in a solution of alkaline peroxide and 75% Celery extract (Apium graveolens L

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Dewi Puspitasari

2016-08-01

Full Text Available Acrylic resin denture base has the properties absorbing that affecting physical and mechanical properties. One of the physical properties of acrylic resin is surface roughness. The aim of the study was to find out the roughness effect on heat cured acrylic that was immersed in alkaline peroxide and 75% celery (Apium graveoens L extract as a disinfectant solution. The study was a true experimental and posttest with control group designed with a rectangular shape size 65 x 10 x 3.3 mm based on the ISO standard 1567, six samples were used for alkaline peroxide, celery extract 75% and aquadest group for 5 and 15 days. A Surface Roughness Tester was used for the surface roughness changes observation. The statistical test used One-way ANOVA and post hoc Bonferroni. The results of this study showed the value of roughness on 5 days for alkaline peroxide (1.51 µm is greater than celery extract (0.36µm and aquadest (0.30 µm. The soaking for 15 days in alkaline peroxide (1.52 µm is greater than 75% celery extracts (0.38 µm and aquadest (0.34 µm. Alkaline peroxide caused higher roughness value of heat cured acrylic resin than 75% celery extract.

The cathodic reduction of dioxygen on uranium oxide in dilute alkaline aqueous solution

International Nuclear Information System (INIS)

Hocking, W.H.; Betteridge, J.S.; Shoesmith, D.W.

1991-09-01

The cathodic reduction of dioxygen on uranium oxide in dilute alkaline aqueous solutions has been investigated within the context of a program to develop a comprehensive model to predict the behaviour of used CANDU (Canada Deuterium Uranium) nuclear fuel under disposal-vault conditions. Two different kinds of ceramic UO 2 were studied: reactor-grade CANDU fuel with normal p-type electrical conductivity and low-resistance material that exhibits n-type photoelectrochemical behaviour. The transport of electroactive species in solution was controlled by varying the rotation rate of rotating disc electrodes (RDE) and rotating ring-disc electrodes (RRDE). Steady-state polarization measurements were made using the current-interrupt method to compensate for the potential drop caused by ohmic resistance. Any release of peroxide to solution from the UO 2 (disc) surface could be monitored by oxidizing it at the Au ring of an RRDE. The existing theory for the cathodic 0 2 -reduction process as applied to RDE and RRDE experiments has been reviewed as a starting point for the interpretation of the results obtained in our work. (37 figs., 2 tabs., 170 refs.)

Galvanic Corrosion between Alloy 690 and Magnetite in Alkaline Aqueous Solutions

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Soon-Hyeok Jeon

2015-12-01

Full Text Available The galvanic corrosion behavior of Alloy 690 coupled with magnetite has been investigated in an alkaline solution at 30 °C and 60 °C using a potentiodynamic polarization method and a zero resistance ammeter. The positive current values were recorded in the galvanic couple and the corrosion potential of Alloy 690 was relatively lower. These results indicate that Alloy 690 behaves as the anode of the pair. The galvanic coupling between Alloy 690 and magnetite increased the corrosion rate of Alloy 690. The temperature increase led to an increase in the extent of galvanic effect and a decrease in the stability of passive film. Galvanic effect between Alloy 690 and magnetite is proposed as an additional factor accelerating the corrosion rate of Alloy 690 steam generator tubing in secondary water.

Radiolytic dimerization of tyrosine in alkaline solutions of poly-L-tyrosine, glycyl-L-tyrosine and tyrosine

International Nuclear Information System (INIS)

Boguta, G.; Dancewicz, A.M.

1982-01-01

Blue fluorescence characteristic of dityrosine appeared in γ-irradiated solutions of tyrosine, glycyl-L-tyrosine or polytyrosine (MW 110,000). The intensity of fluorescence was used for the determination of the dityrosine concentration in hydrolysed samples. The radiation-induced formation of dityrosine depended on pH and on the presence of oxygen during radiolysis carried out with a total dose of the order of 1000 Gy. The presence of oxygen in the system suppressed the formation of dityrosine in solution at low or neutral pH but had no effect on this process in alkaline solutions. Except for the radiolysis of air-saturated poly-L-tyrosine solutions, where G(Dityrosine) = 0.35, the yields of dityrosine at high pH were lower than the yields obtained during radiolysis at low pH and in the absence of oxygen. (author)

COUPLING THE ALKALINE-SURFACTANT-POLYMER TECHNOLOGY AND THE GELATION TECHNOLOGY TO MAXIMIZE OIL PRODUCTION

Energy Technology Data Exchange (ETDEWEB)

Malcolm Pitts; Jie Qui; Dan Wilson; Phil Dowling

2004-05-01

Gelation technologies have been developed to provide more efficient vertical sweep efficiencies for flooding naturally fractured oil reservoirs or more efficient areal sweep efficiency those with high permeability contrast ''thief zones''. The field proven alkaline-surfactant-polymer technology economically recovers 15% to 25% OOIP more oil than waterflooding in the swept pore space of an oil reservoir. However, alkaline-surfactant-polymer technology is not amenable to the naturally fractured reservoirs or those with thief zones because much of the injected solution bypasses the target pore space containing oil. The objective of this work is to investigate whether combining these two technologies could broaden the applicability of alkaline-surfactant-polymer flooding into these reservoirs. Fluid-fluid interaction with different gel chemical compositions and alkaline-surfactant-polymer solution with pH values ranging from 9.2 to 12.9 have been tested. Aluminum-polyacrylamide gels are not stable to alkaline-surfactant-polymer solutions at any pH. Chromium--polyacrylamide gels with polymer to chromium ion ratios of 25 or greater were stable to alkaline-surfactant-polymer solutions if solution pH was 10.6 or less. When the polymer to chromium ion was 15 or less, chromium-polyacrylamide gels were stable to alkaline-surfactant-polymer solutions with pH values up to 12.9. Chromium-xanthan gum gels were stable to alkaline-surfactant-polymer solutions with pH values of 12.9 at the polymer to chromium ion ratios tested. Silicate-polyacrylamide, resorcinol-formaldehyde, and sulfomethylated resorcinol-formaldehyde gels were also stable to alkaline-surfactant-polymer solutions with pH values ranging from 9.2 to 12.9. Iron-polyacrylamide gels were immediately destroyed when contacted with any of the alkaline-surfactant-polymer solutions with pH values of 9.2 to 12.9.

Grain size effect in corrosion behavior of electrodeposited nanocrystalline Ni coatings in alkaline solution

International Nuclear Information System (INIS)

Wang Liping; Zhang Junyan; Gao Yan; Xue Qunji; Hu Litian; Xu Tao

2006-01-01

Effects of grain size reduction on the electrochemical corrosion behavior of nanocrystalline Ni produced by pulse electrodeposition were characterized using potentiodynamic polarization testing and electrochemical impedance spectroscopy; X-ray photoelectron spectroscopy were used to confirm the electrochemical measurements and the suggested mechanisms. The corrosion resistance of Ni coatings in alkaline solutions considerably increased as the grain size decreased from microcrystalline to nanocrystalline. The higher corrosion resistance of NC Ni may be due to the more rapid formation of continuous Ni(OH) 2 passive films compared with coarse-grained Ni coatings

On performance capabilities of alkaline anolyte in wastewater management

International Nuclear Information System (INIS)

Shimkevich, Alexander

2014-01-01

A concept for electric converting a saline wastewater into basic solution (pH > 7) with a positive RedOx potential (alkaline anolyte) is considered. Such the medium can be obtained in situ at flowing wastewater via a special electrochemical cell with strongly polarized cathode (generating hydroxide anions) and quasi-equilibrium anode which intensively discharges hydroxide ions to hydroxyl radicals into the wastewater. The radicals will oxidize anions of strong acid and convert them into weak-acid micro precipitates in the flowing basic solution. These renewable nano-sorbents will uninterruptedly co-precipitate radioactive contamination from wastewater and be agglomerated as corrosion by-products in the felt-like anode. The consideration of liquid water as a chemical compound with a wide band gap shows that the anolyte (as a hyper-stoichiometric water, H 2 O 1+|x| ) is a simple and effective tool for varying physical and chemical properties of the aqueous solution due to forced changing its RedOx potential as one needs. This potential as Fermi level in the band gap of liquid water is the most convenient parameter for monitoring and managing the electrochemical potential of the aqueous medium. Its hyper-stoichiometric state is realized when Fermi level is shifted to the top of a valence band. This electro-oxidized state as the alkaline anolyte is characterized by an acceptor level, OH/OH - , partially occupied by electrons. Then, the hydroxyl radical (OH • ) as the strongest oxidizer will oxidize intensively the metal anode and renew its surface for great removal of radio-nuclides from the wastewater due to their large specific area of renewable surface of hydroxide absorber on the felt-like anode. (author)

Treatment of infectious skin defects or ulcers with electrolyzed strong acid aqueous solution.

Science.gov (United States)

Sekiya, S; Ohmori, K; Harii, K

1997-01-01

A chronic ulcer with an infection such as methicillin-resistant Staphylococcus aureus is hard to heal. Plastic and reconstructive surgeons often encounter such chronic ulcers that are resistant to surgical or various conservative treatments. We applied conservative treatment using an electrolyzed strong acid aqueous solution and obtained satisfactory results. The lesion was washed with the solution or soaked in a bowl of the solution for approximately 20 min twice a day. Fresh electrolyzed strong acid aqueous solution is unstable and should be stored in a cool, dark site in a sealed bottle. It should be used within a week after it has been produced. Here we report on 15 cases of infectious ulcers that were treated by electrolyzed strong acid aqueous solution. Of these cases, 7 patients were healed, 3 were granulated, and in 5, infection subsided. In most cases the lesion became less reddish and less edematous. Discharge or foul odor from the lesion was decreased. Electrolyzed strong acid aqueous solution was especially effective for treating a chronic refractory ulcer combined with diabetes melitus or peripheral circulatory insufficiency. This clinically applied therapy of electrolyzed strong acid aqueous solution was found to be effective so that this new therapeutic technique for ulcer treatment can now be conveniently utilized.

Evaluation of hydraulic conductivities of bentonite and rock under hyper alkaline and nitrate conditions. 2

International Nuclear Information System (INIS)

Iriya, Keishiro; Fujii, Kensuke; Kubo, Hiroshi

2003-02-01

Circumstance of TRU waste repository shows alkaline condition due to leaching of cementitious materials. The waste containing significant soluble nitrate may changes ground water chemistry to high ion strength. Several experimental studies have been carried out in this study in order to assess quantitatively water conductivity of bentonite which is altered by hyper alkaline and nitrate. Modeling for previous results is carried out and several requirements to be defined are proposed. The conclusion of this study is summarized as below. Secondary minerals of bentonite alteration due to hyper alkaline with nitrate: 1) CSH and CAH were observed corresponding to solving montmorillonite in AWN solution. 2) Na 2 O Al 2 O 3 1.68SiO 2 generated from 90 days in batch experiment and it was observed in 360 days. Assessment of swelling and water conductivity changing by hyper alkaline with nitrate: 1) Little changing of water conductivity of bentonite was observed by saturated Ca(OH) 2 solution and hyper alkaline solution. The conductivity significantly increased by penetrating sodium nitrate solution. 2) Water conductivity of ion exchanged bentonite by hyper alkaline solution significantly increased. It increased more by penetrating AWN solution. Modeling of tuff alteration by hyper alkaline solution: 1) Flow through test is proposed since soluble velocity to hyper alkaline solution should be defined. (author)

Establishing the potential dependent equilibrium oxide coverage on platinum in alkaline solution and its influence on the oxygen reduction

DEFF Research Database (Denmark)

Wiberg, Gustav; Arenz, Matthias

2012-01-01

Publication year: 2012 Source:Journal of Power Sources, Volume 217 Gustav K.H. Wiberg, Matthias Arenz The oxidation process of polycrystalline platinum subjected to alkaline solution is re-examined using a combination of cyclic voltammetry and potential hold techniques in Ar, H2 and O2 purged 0.1...

Chemically and compositionally modified solid solution disordered multiphase nickel hydroxide positive electrode for alkaline rechargeable electrochemical cells

Science.gov (United States)

Ovshinsky, Stanford R.; Corrigan, Dennis; Venkatesan, Srini; Young, Rosa; Fierro, Christian; Fetcenko, Michael A.

1994-01-01

A high capacity, long cycle life positive electrode for use in an alkaline rechargeable electrochemical cell comprising: a solid solution nickel hydroxide material having a multiphase structure that comprises at least one polycrystalline .gamma.-phase including a polycrystalline .gamma.-phase unit cell comprising spacedly disposed plates with at least one chemical modifier incorporated around the plates, the plates having a range of stable intersheet distances corresponding to a 2.sup.+ oxidation state and a 3.5.sup.+, or greater, oxidation state; and at least one compositional modifier incorporated into the solid solution nickel hydroxide material to promote the multiphase structure.

Pitting corrosion of friction stir welded aluminum alloy thick plate in alkaline chloride solution

International Nuclear Information System (INIS)

Xu Weifeng; Liu Jinhe; Zhu Hongqiang

2010-01-01

The pitting corrosion of different positions (Top, Middle and Bottom) of weld nugget zone (WNZ) along thickness plate in friction stir welded 2219-O aluminum alloy in alkaline chloride solution was investigated by using open circuit potential, cyclic polarization, scanning electron microscopy and atomic force microscope. The results indicate that the material presents significant passivation, the top has highest corrosion potential, pitting potential and re-passivation potential compared with the bottom and base material. With the increase of traverse speed from 60 to 100 mm/min or rotary speed from 500 to 600 rpm, the corrosion resistance decreases.

COUPLING THE ALKALINE-SURFACTANT-POLYMER TECHNOLOGY AND THE GELATION TECHNOLOGY TO MAXIMIZE OIL PRODUCTION

Energy Technology Data Exchange (ETDEWEB)

Malcolm Pitts; Jie Qi; Dan Wilson

2004-10-01

Gelation technologies have been developed to provide more efficient vertical sweep efficiencies for flooding naturally fractured oil reservoirs or more efficient areal sweep efficiency for those with high permeability contrast ''thief zones''. The field proven alkaline-surfactant-polymer technology economically recovers 15% to 25% OOIP more oil than waterflooding from swept pore space of an oil reservoir. However, alkaline-surfactant-polymer technology is not amenable to naturally fractured reservoirs or those with thief zones because much of injected solution bypasses target pore space containing oil. This work investigates whether combining these two technologies could broaden applicability of alkaline-surfactant-polymer flooding into these reservoirs. A prior fluid-fluid report discussed interaction of different gel chemical compositions and alkaline-surfactant-polymer solutions. Gel solutions under dynamic conditions of linear corefloods showed similar stability to alkaline-surfactant-polymer solutions as in the fluid-fluid analyses. Aluminum-polyacrylamide, flowing gels are not stable to alkaline-surfactant-polymer solutions of either pH 10.5 or 12.9. Chromium acetate-polyacrylamide flowing and rigid flowing gels are stable to subsequent alkaline-surfactant-polymer solution injection. Rigid flowing chromium acetate-polyacrylamide gels maintained permeability reduction better than flowing chromium acetate-polyacrylamide gels. Silicate-polyacrylamide gels are not stable with subsequent injection of either a pH 10.5 or a 12.9 alkaline-surfactant-polymer solution. Neither aluminum citrate-polyacrylamide nor silicate-polyacrylamide gel systems produced significant incremental oil in linear corefloods. Both flowing and rigid flowing chromium acetate-polyacrylamide gels produced incremental oil with the rigid flowing gel producing the greatest amount. Higher oil recovery could have been due to higher differential pressures across cores. None of

Oxidation of D-glucose and D-fructose with oxygen in aqueous, alkaline solutions. III. Kinetic approach to the product distribution

NARCIS (Netherlands)

de Wilt, H.G.J.; Kuster, Ben

1972-01-01

Based on a previously reported, integral reaction-scheme for the homogeneous oxidation of -glucose and -fructose with oxygen in aqueous, alkaline solutions, a kinetic model covering the product distribution has been developed. The model consists of a repeated set of reactions with constant rate

Study of niobium corrosion in alkaline medium

International Nuclear Information System (INIS)

Almeida, S.H. de.

1987-01-01

A comparative study of niobium electrochemical behaviour in NaOH and KOH solution, with concentrations between 0,5 and 6,1M is presented. The studies were done through electrochemicals assays, consisting in the corrosion potential and anodic and cathodic polarization curves, complemented by loss of mass experiments. The niobium anodic behaviour in alkaline medium is characterized by passivation occurrence, with a stable film formation. The Na oH solution in alkaline medium are more corrosible to niobium than the KOH solution. The loss of mass assays showed that the corrosion velocit is more dependente of hydroxide concentration in KOH medium than the NaOH medium. (C.G.C.) [pt

Isolation of radioactive strontium from natural samples. Separation of strontium from alkaline and alkaline earth elements by means of mixed solvent anion exchange

International Nuclear Information System (INIS)

Grahek, Z.; Kosutic, K.; Lulic, S.; Kvastek, K.; Eskinja, I.

1999-01-01

This paper presents the results of studies which led to the procedures for the chromatographic separation of radioactive strontium from alkaline, earth-alkaline and other elements in natural samples, on columns filled with strong base anion exchangers using alcoholic solutions of nitric acid as eluents. It has been shown that potassium, caesium, calcium, barium, yttrium and strontium can be adsorbed on strong base anion exchangers of the Dowex and Amberlite type, which contain the quaternary ammonium group with nitrate as counter-ion, from solutions of nitric acid in alcohol. Adsorption strength increases in the order methanol 3 in methanol, while they are adsorbed from ethanol and propanol. The adsorption strength is influenced by the polarity of alcohol, by the concentration of nitrate and by pH. The strength with which strontium adsorbs on the exchangers increases in the interval from 0 to 0.25M NH 4 NO 3 in methanol, after which it starts to decrease. Strontium adsorbs to the exchangers from the alcoholic solution of ammonium nitrate twice as strongly as from the alcoholic solution of nitric acid, while a fraction of water in pure alcohol exceeding 10% prevents adsorption. In the mixture of alcohol and nitric acid, the adsorption strength for calcium and strontium increases with the increase of the volume fraction of alcohol with a lower dielectric constant. The rate and strength of adsorption of ions on the exchanger also increase in the series 0.25M HNO 3 in methanol 3 in ethanol 3 in 1-propanol for each individual ion, as well as in the Ca 3 in methanol, 0.25M HNO 3 in ethanol and 0.25M HNO 3 in propanol. Separation is also possible from alcohol mixtures. Strontium separation is most difficult from calcium, while the efficiency of separation increases with a decrease of the polarity of the used alcohol or alcohol mixture. The first group elements of the periodic table are not separated from each other in this way, while the elements of the second group are

Effect of alkaline cleaning and activation on aluminum alloy 7075-T6

International Nuclear Information System (INIS)

Joshi, Simon; Fahrenholtz, William G.; O'Keefe, Matthew J.

2011-01-01

The effect of alkaline cleaning and activation on the composition and thickness of the oxide layer on aluminum alloy 7075-T6 was studied. E-pH diagrams were developed to predict the effect of alkaline cleaning and activation solutions on the stability of the oxide surface layers. The thickness of the native oxide layer was determined to be ∼30 nm by Auger electron spectroscopy depth profiling analysis. The outer ∼20 nm was rich in magnesium while the remaining ∼10 nm was rich in aluminum. Cleaning in a 9.1 pH alkaline solution was found to remove the magnesium-rich layer and leave behind an aluminum-rich oxide layer ∼10 nm thick. Activation in alkaline solutions of NaOH (pH > 12.9) or Na 2 CO 3 (pH > 11.5) produced an oxide that was ∼20 to 60 nm thick and rich in magnesium. Alkaline cleaning and activation altered the oxide composition and thickness making it possible for deposition of thicker cerium-based conversion coatings (∼100 to 250 nm) compared to only alkaline cleaning (∼30 nm), with application of one spray cycle of deposition solution.

Effect of alkaline cleaning and activation on aluminum alloy 7075-T6

Energy Technology Data Exchange (ETDEWEB)

Joshi, Simon, E-mail: sjwt5@mst.edu [Department of Materials Science and Engineering, Missouri University of Science and Technology, Rolla, MO 65409 (United States); Fahrenholtz, William G.; O' Keefe, Matthew J. [Department of Materials Science and Engineering, Missouri University of Science and Technology, Rolla, MO 65409 (United States)

2011-01-01

The effect of alkaline cleaning and activation on the composition and thickness of the oxide layer on aluminum alloy 7075-T6 was studied. E-pH diagrams were developed to predict the effect of alkaline cleaning and activation solutions on the stability of the oxide surface layers. The thickness of the native oxide layer was determined to be {approx}30 nm by Auger electron spectroscopy depth profiling analysis. The outer {approx}20 nm was rich in magnesium while the remaining {approx}10 nm was rich in aluminum. Cleaning in a 9.1 pH alkaline solution was found to remove the magnesium-rich layer and leave behind an aluminum-rich oxide layer {approx}10 nm thick. Activation in alkaline solutions of NaOH (pH > 12.9) or Na{sub 2}CO{sub 3} (pH > 11.5) produced an oxide that was {approx}20 to 60 nm thick and rich in magnesium. Alkaline cleaning and activation altered the oxide composition and thickness making it possible for deposition of thicker cerium-based conversion coatings ({approx}100 to 250 nm) compared to only alkaline cleaning ({approx}30 nm), with application of one spray cycle of deposition solution.

Another intermediate in the photochemistry and radiation chemistry of alkaline aqueous solutions

International Nuclear Information System (INIS)

Telser, T.; Schindewolf, U.

1985-01-01

By UV flash photolytic and pulse radiolytic experiments of aqueous alkaline solutions we confirm older experiments of Walker et al. and Hart et al., showing that the decay of hydrated electrons gives rise to another intermediate X which by light absorption revives hydrated electrons again. X is formed by a reaction of 1. order with respect to hydrated electrons, the rate of its formation increases with pH, and it decays by a second order process with a rate constant not exceeding 5 . 10 9 M -1 sec -1 , probably leading to hydrogen (e - ->X; 2X->H 2 ). X has maximum light absorption around 270 nm with an extinction coefficient of about 5000 M -1 cm -1 . We will not speculate about the nature of X. (orig.)

Photolysis of Periodate and Periodic Acid in Aqueous Solution

DEFF Research Database (Denmark)

Sehested, Knud; Kläning, U. K.

1978-01-01

The photochemistry of periodate and periodic acid in aqueous solution was studied (i) by quantum yield measurements at low light intensity (ii) by flash photolysis, and (iii) by photolysis of glassy samples at 77 K. The photochemical studies were supplemented with pulse radiolysis studies...... of aqueous periodate solutions and with kinetic studies using stopped-flow technique. In strongly alkaline solution the photodecomposition of periodate proceeds via formation of O– and IVI. At pH solution O3 P is formed in a small...

Application of alkaline waterflooding to a high acidity crude oil

Energy Technology Data Exchange (ETDEWEB)

Sayyouh, M.H. (King Sand Univ., Riyadh (SA). Petroleum Engineering Dept.); Abdel-Waly, A.; Osman, A. (Cairo Univ. (EG). Petroleum Engineering Dept.); Awara, A.Z. (Geisum Oil Company, Cairo (EG))

The enhanced recovery of a high acidity crude oil (South Geisum crude) by alkaline solutions is studied. Acidity, interfacial tension, and contact angle, were investigated. Displacement tests were carried out to study the effect of alkaline slug concentration, slug size, oil alkali type, temperature and viscosity on recovery. The interfacial tension between crude oil and formation water decreases with increasing alkaline concentration until a minimum, after which it increases again. Contact angle measurements indicated oil-wetting conditions that increase by the addition of alkaline solutions. At the early stages of displacement, oil recovery increases with increasing alkaline concentration until a maximum at 4% by weight NaOH concentration. Also, at such early stages, an excessive increase in alkaline concentration results in lower oil recovery. On the other hand, after the injection of many pore volumes of water, oil recovery is almost the same regardless of the alkaline concentration. Oil recovery increases with increasing alkaline slug size until a maximum at 15% PV. Sodium hydroxide slugs produce more oil recovery than sodium carbonate slugs. Oil recovery increases with increasing temperature (from 25 to 55{sup 0}C) and decreasing oil viscosity.

The interaction of Np(V), Pu(VI) and Tc(VII) with metal in alkaline solutions

International Nuclear Information System (INIS)

Silin, V.I.; Kareta, A.V.

1998-01-01

The interaction of Np(V), Pu(VI) and Tc(VII) with metal reductants Zn, Cr, Sn and their alloys was investigated in 0.5-4 mol l -1 NaOH solutions in static and dynamic conditions (by filtration of solutions through the column filled with grains of metal). In this paper, it was found that the reduction and succeeding precipitation hydroxides of these elements, on the surface of metal grains from 0.5 to 4 mol l -1 NaOH solutions, gives a decontamination factor (DF) from 1.1 to 67. The best result was achieved for Pu (DF=67) on Cr grains after 2.5 h contact at 60 C with 0.5 mol l -1 NaOH solution containing Pu(VI). Increasing the NaOH concentration, and the addition of chromate ions and complex-forming agents to alkaline solution results in a decrease of the decontamination factor (DF). A better result for Np sorption from 1 mol l -1 NaOH solutions was achieved after longer contact, than for Pu, with Cr and Zn grains. The maximum DF=8.9 was achieved for Tc on a column with Zn grains after filtration with a 3.5 mol l -1 NaOH solution containing Tc(VII). Washing out of Np and Pu, sorbed on the Cr grain surfaces, was achieved using an acid solution (1 mol l -1 HNO 3 ). The technetium was desorbed from metal surface by 10% H 2 O 2 solution. (orig.)

An in situ Fourier transform infrared spectroelectrochemical study on ethanol electrooxidation on Pd in alkaline solution

Energy Technology Data Exchange (ETDEWEB)

Fang, Xiang; Wang, Lianqin; Shen, Pei Kang [The State Key Laboratory of Optoelectronic Materials and Technologies, School of Physics and Engineering, Sun Yat-Sen University, Guangzhou 510275 (China); Cui, Guofeng [School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275 (China); Bianchini, Claudio [Istituto di Chimica dei Composti Organometallici (ICCOM-CNR), via Madonna del Piano 10, 50019 Sesto Fiorentino (Italy)

2010-03-01

The mechanism of ethanol electrooxidation on a palladium electrode in alkaline solution (from 0.01 to 5 M NaOH) has been investigated by cyclic voltammetry and in situ Fourier transform infrared spectroelectrochemistry. The electrode performance has been found to depend on the pH of the fuel solution. The best performance was observed in 1 M NaOH solution (pH = 14), while the electrochemical activity decreased by either increasing or decreasing the NaOH concentration. In situ FTIR spectroscopic measurements showed the main oxidation product to be sodium acetate at NaOH concentrations higher than 0.5 M. The C-C bond cleavage of ethanol, put in evidence by the formation of CO{sub 2}, occurred at pH values {<=}13. In these conditions, however, the catalytic activity for ethanol oxidation was quite low. No CO formation was detected along the oxidation of ethanol by FTIR spectroscopy. (author)

The reactivity of the electron formed in the radiolysis of aerated alkaline aqueous solutions containing tetracycline hydrochloride, at 77 Ksup(+)

International Nuclear Information System (INIS)

Guedes, S.M.L.; Vasconcellos, M.B.A.

1986-01-01

The radiolysis of tetracycline hydrochloride dissolved in aerated alkaline aqueous solutions containing 0.1, 0.5 and 1M NaOH at 77 K, followed by ESR is reported. The rate constants for the reactions between the electron and physical or chemical traps which are present in these solutions are calculated. The reactivity of electrons that are formed in the radiolysis of water decreases in the following proportions: physical traps: chemical traps: molecules of water (4.8x10sup(14) : 6.5x10sup(8) : 1.0). The electrons react preferentially with the solute instead of the solvent. (author)

Effect of the nature of alkali and alkaline-earth oxides on the structure and crystallization of an alumino-borosilicate glass developed to immobilize highly concentrated nuclear waste solutions

International Nuclear Information System (INIS)

Quintas, A.; Caurant, D.; Majerus, O.; Charpentier, T.; Dussossoy, J.L.

2008-01-01

A complex rare-earth rich alumino-borosilicate glass has been proved to be a good candidate for the immobilization of new high level radioactive wastes. A simplified seven-oxides composition of this glass was selected for this study. In this system, sodium and calcium cations were supposed in other works to simulate respectively all the other alkali (R + = Li + , Rb + , Cs + ) and alkaline-earth (R 2+ = Sr 2+ , Ba 2+ ) cations present in the complex glass composition. Moreover, neodymium or lanthanum are used here to simulate all the rare-earths and actinides occurring in waste solutions. In order to study the impact of the nature of R + and R 2+ cations on both glass structure and melt crystallization tendency during cooling, two glass series were prepared by replacing either Na + or Ca 2+ cations in the simplified glass by respectively (Li + , K + , Rb + , Cs + ) or (Mg 2+ , Sr 2+ , Ba 2+ ) cations. From these substitutions, it was established that alkali ions are preferentially involved in the charge compensation of (AlO 4 ) - entities in the glass network comparatively to alkaline-earth ions. The glass compositions containing calcium give way to the crystallization of an apatite silicate phase bearing calcium and rare-earth ions. The melt crystallization tendency during cooling strongly varies with the nature of the alkaline-earth. (authors)

High-Efficiency Artificial Photosynthesis Using a Novel Alkaline Membrane Cell

Science.gov (United States)

Narayan, Sri; Haines, Brennan; Blosiu, Julian; Marzwell, Neville

2009-01-01

A new cell designed to mimic the photosynthetic processes of plants to convert carbon dioxide into carbonaceous products and oxygen at high efficiency, has an improved configuration using a polymer membrane electrolyte and an alkaline medium. This increases efficiency of the artificial photosynthetic process, achieves high conversion rates, permits the use of inexpensive catalysts, and widens the range of products generated by this type of process. The alkaline membrane electrolyte allows for the continuous generation of sodium formate without the need for any additional separation system. The electrolyte type, pH, electrocatalyst type, and cell voltage were found to have a strong effect on the efficiency of conversion of carbon dioxide to formate. Indium electrodes were found to have higher conversion efficiency compared to lead. Bicarbonate electrolyte offers higher conversion efficiency and higher rates than water solutions saturated with carbon dioxide. pH values between 8 and 9 lead to the maximum values of efficiency. The operating cell voltage of 2.5 V, or higher, ensures conversion of the carbon dioxide to formate, although the hydrogen evolution reaction begins to compete strongly with the formate production reaction at higher cell voltages. Formate is produced at indium and lead electrodes at a conversion efficiency of 48 mg of CO2/kilojoule of energy input. This efficiency is about eight times that of natural photosynthesis in green plants. The electrochemical method of artificial photosynthesis is a promising approach for the conversion, separation and sequestration of carbon dioxide for confined environments as in space habitats, and also for carbon dioxide management in the terrestrial context. The heart of the reactor is a membrane cell fabricated from an alkaline polymer electrolyte membrane and catalyst- coated electrodes. This cell is assembled and held in compression in gold-plated hardware. The cathode side of the cell is supplied with carbon

Effect of clay content in rock on oil extraction under alkaline seam conditions

Energy Technology Data Exchange (ETDEWEB)

Vezirov, D Sh; Gorbunov, A T; Kasimov, Sh A; Kashchavtsev, V E; Tairov, N D

1978-01-01

When oil beds are flooded with alkaline solutions, the alkaline concentration in the solution can be significantly reduced as a result of the interaction between clay and alkali. Large losses of alkali in the bed can render the flooding method ineffective. Experimental studies were conducted on porous media containing up to 25% clay at a constant permeability of 1 D in order to determine the oil extraction indices for clay-containing rock. Constant permeability is maintained by using clays, marshalite, and quartz sand in various proportions. Oil having a viscosity of 99.17 sP, and containing a large amount of surfactants, including 1.1% naphthenic acid, was extracted by fresh water and a 0.25% solution of NaOH. The extraction of oil by fresh water and NaOH solution from quartz sand indicated the advantage of using alkaline solutions. The extraction coefficient increased by 11% with the use of this method. As clay is added to the sand, the extraction coefficient decreases, and is reduced to 12.7% when the clay content reaches 25%. Nevertheless, a comparison of data obtained for quartz sand with fresh water on a porous medium containing 25% clay with an alkaline solution, indicates that the extraction coefficient is just 1.5% lower even in the presence of such a large amount of clay. Consequently, alkaline flooding should still be given preference over the usual methods under specific conditions and where the rock has a comparatively large amount of clay, in view of all the basic factors that influence the extraction process. The results obtained can be used for selecting alkaline concentration in evaluating the efficiency of flooding oil beds with alkaline solutions. 2 figures, 2 tables.

Isotherms of ion exchange on titanates of alkaline metals

International Nuclear Information System (INIS)

Fillina, L.P.; Belinskaya, F.A.

1986-01-01

Present article is devoted to isotherms of ion exchange on titanates of alkaline metals. Therefore, finely dispersed hydrated titanates of alkaline metals (lithium, sodium, potassium) with ion exchange properties are obtained by means of alkaline hydrolysis of titanium chloride at high ph rates. Sorption of cations from salts solution of Li 2 SO 4 , NaNO 3 , Ca(NO 3 ) 2 , AgNO 3 by titanates is studied.

Investigation of electrochemical synthesis of ferrate, Part I: Electrochemical behavior of iron and its several alloys in concentrated alkaline solutions

Directory of Open Access Journals (Sweden)

Čekerevac Milan I.

2009-01-01

cyclic voltammetry, galvanostatic and potentiostatic pulse method. Cyclic voltammetry gave useful data on potential regions where ferrate(VI formation is to be expected in the course of transpassive anodic oxidation of iron and some of its alloys, and its stability in the electrolytes of different composition. In addition, step-wise oxidation of iron in anodic oxidation is confirmed. Galvanostatic pulse experiments confirmed the character of successive anodic oxidation of iron, as the three-step process of ferrate(VI formation is clearly observed. In the cathodic pulse complex reduction of ferrate (VI, firstly to Fe(III species and then to mixed Fe(II and Fe(III compounds and finally to elementary iron is confirmed. The significant difference between the mechanisms of anodic oxidation of pure iron and low carbon steel at the one side and electrical ferrous-silicon steel at the other is observed. The influence of material chemical composition on the electrochemical behavior of electrode in course of anodic polarization in strong alkaline solutions is discussed in terms of composition of passivating layer formed on the electrode. On the base of the experimental data, efficient synthesis of ferrate(VI can be expected in the region of anodic potentials between + 0,55 and + 0,75 V against Hg|HgO reference electrode in the same solution, depending on the anode materials composition, in the alkaline electrolytes concentration between 10 and 15 M.

Inorganic polymers from laterite using activation with phosphoric acid and alkaline sodium silicate solution: Mechanical and microstructural properties

Energy Technology Data Exchange (ETDEWEB)

Lassinantti Gualtieri, Magdalena, E-mail: magdalena.gualtieri@unimore.it [Dipartimento di Ingegneria " Enzo Ferrari" , Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy); Romagnoli, Marcello [Dipartimento di Ingegneria " Enzo Ferrari" , Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy); Pollastri, Simone; Gualtieri, Alessandro F. [Dipartimento di Scienze Chimiche e Geologiche, Università degli studi di Modena e Reggio Emilia, Via S. Eufemia 19I, I-41121 Modena (Italy)

2015-01-15

Geopolymers from laterite, an iron-rich soil available in developing countries, have great potential as building materials. In this work, laterite from Togo (Africa) was used to prepare geopolymers using both phosphoric acid and alkaline sodium silicate solution. Microstructural properties were investigated by scanning electron microscopy, X-ray powder diffraction and mercury porosimetry, whereas thermal properties were evaluated by thermal analyses. The local environment of iron was studied by X-ray Absorption Spectroscopy (XANES region). The mechanical properties were determined. Modulus of Rupture and Young's modulus fell in the ranges 3.3–4.5 MPa and 12–33 GPa, respectively, rendering the materials good candidates for construction purposes. Heating above 900 °C results in weight-gain, presumably due to iron redox reactions. X-ray Absorption Spectroscopy data evidence changes in the chemical and structural environments of iron following thermal treatment of geopolymers. These changes indicate interaction between the geopolymer structure and iron during heating, possibly leading to redox properties. -- Highlights: •Geopolymerization of laterite is promising for fabrication of building materials. •Both phosphoric acid and alkaline sodium silicate solution can be used for activation. •Thermally activated redox properties of the inorganic polymers were observed.

Inorganic polymers from laterite using activation with phosphoric acid and alkaline sodium silicate solution: Mechanical and microstructural properties

International Nuclear Information System (INIS)

Enzo Ferrari, Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy))" data-affiliation=" (Dipartimento di Ingegneria Enzo Ferrari, Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy))" >Lassinantti Gualtieri, Magdalena; Enzo Ferrari, Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy))" data-affiliation=" (Dipartimento di Ingegneria Enzo Ferrari, Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy))" >Romagnoli, Marcello; Pollastri, Simone; Gualtieri, Alessandro F.

2015-01-01

Geopolymers from laterite, an iron-rich soil available in developing countries, have great potential as building materials. In this work, laterite from Togo (Africa) was used to prepare geopolymers using both phosphoric acid and alkaline sodium silicate solution. Microstructural properties were investigated by scanning electron microscopy, X-ray powder diffraction and mercury porosimetry, whereas thermal properties were evaluated by thermal analyses. The local environment of iron was studied by X-ray Absorption Spectroscopy (XANES region). The mechanical properties were determined. Modulus of Rupture and Young's modulus fell in the ranges 3.3–4.5 MPa and 12–33 GPa, respectively, rendering the materials good candidates for construction purposes. Heating above 900 °C results in weight-gain, presumably due to iron redox reactions. X-ray Absorption Spectroscopy data evidence changes in the chemical and structural environments of iron following thermal treatment of geopolymers. These changes indicate interaction between the geopolymer structure and iron during heating, possibly leading to redox properties. -- Highlights: •Geopolymerization of laterite is promising for fabrication of building materials. •Both phosphoric acid and alkaline sodium silicate solution can be used for activation. •Thermally activated redox properties of the inorganic polymers were observed

Processing Methods of Alkaline Hydrolysate from Rice Husk

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Olga D. Arefieva

2017-07-01

Full Text Available This paper devoted to finding processing methods of alkaline hydrolysate produced from rice husk pre-extraction, and discusses alkaline hydrolysate processing schemed and disengagement of some products: amorphous silica of various quality, alkaline lignin, and water and alkaline extraction polysaccharides. Silica samples were characterized: crude (air-dried, burnt (no preliminary water treatment, washed in distilled water, and washed in distilled water and burnt. Waste water parameters upon the extraction of solids from alkaline hydrolysate dropped a few dozens or thousand times depending on the applied processing method. Color decreased a few thousand times, turbidity was virtually eliminated, chemical oxygen demanded about 20–136 times; polyphenols content might decrease 50% or be virtually eliminated. The most prospective scheme obtained the two following solid products from rice husk alkaline hydrolysate: amorphous silica and alkaline extraction polysaccharide. Chemical oxygen demand of the remaining waste water decreased about 140 times compared to the silica-free solution.

Application of Resin in Pulp Technique for Ion Exchange Separation of Uranium from Alkaline Leachate

International Nuclear Information System (INIS)

Sreenivas, T.; Rajan, K.C.; Chakravartty, J.K.

2014-01-01

Conclusions: • Resin-in-pulp technique was applied for purification and enrichment of uranium values from a finely ground uranium ore leach slurry of alkaline nature using strong base anion exchange resin (size 500 - 675μm). • The chemical composition of the solution phase of the alkaline leach slurry (pH 9.5) was consisting of about 40 g/L of total dissolved solutes (TDS) predominantly with Na_2CO_3 and NaHCO_3 and minor levels of Na_2SO_4. The uranium content was only 730 mg/L and d50 of solids was 34μm. • Amongst the various commercially available resins studied PFA 4740 and 4783 having quaternary ammonium ion on polystyrene crosslink with divibyl benzez (DVB) gave best performance. The maximum loading capacity achieved in the RIP studies was about 60-65 g of U_3O_8/L of wet settled resin amounting to 98% of loading. This has necessitated 4 stages of counter-current extraction with overall contact time of 100 minutes at a resin to leach slurry volume ratio of about 1:50. Practically the entire uranium values loaded on the resin were eluted using NaCl. • The RIP process was found quite efficient for uranium bearing alkaline leach slurries.

Cation exchange properties of zeolites in hyper alkaline aqueous media.

Science.gov (United States)

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

2015-02-03

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

Research on killing Escherichia Coli by reactive oxygen species based on strong ionization discharging plasma

International Nuclear Information System (INIS)

Li, Y J; Tian, Y P; Zhang, Z T; Li, R H; Cai, L J; Gao, J Y

2013-01-01

Reactive oxygen species solution produced by strong ionization discharging plasma was used to kill Escherichia coli by spraying. Several effect factors such as pH value, solution temperature, spraying time and exposure time were observed in this study, and their effects on killing rate of Escherichia coli were discussed and analysed. Results show that the treating efficiency of ROS solution for Escherichia coli is higher in alkaline solution than that in acid solution. The killing rate of Escherichia coli increases while the spraying time and exposure time are longer and the temperature is lower. The effects of different factors on killing rate of Escherichia coli are as follows: spraying time > pH value > exposure time > solution temperature.

High-pressure densified solid solutions of alkaline earth hexaborides (Ca/Sr, Ca/Ba, Sr/Ba) and their high-temperature thermoelectric properties

International Nuclear Information System (INIS)

Gürsoy, M.; Takeda, M.; Albert, B.

2015-01-01

Solid solutions of alkaline earth hexaborides were synthesized and densified by spark plasma sintering at 100 MPa. The high-temperature thermoelectric properties (Seebeck coefficients, electrical and thermal diffusivities, heat capacities) were measured between room temperature and 1073 K. CaB 6 , SrB 6 , BaB 6 and the ternary hexaborides Ca x Sr 1−x B 6 , Ca x Ba 1−x B 6 , Sr x Ba 1−x B 6 (x = 0.25, 0.5, 0.75) are n-type conducting compounds over the whole compositional and thermal ranges. The values of the figure of merit ZT for CaB 6 (ca. 0.3 at 1073 K) were found to be significantly increased compared to earlier investigations which is attributed to the densification process. - Highlights: • Solid solutions of alkaline earth hexaborides were synthesized. • High-temperature thermoelectric properties of mixed calcium borides are excellent. • Spark plasma source densification results in high ZT values. • Borides are rare-earth free and refractory materials

Zinc electrodeposition from flowing alkaline zincate solutions: Role of hydrogen evolution reaction

Science.gov (United States)

Dundálek, Jan; Šnajdr, Ivo; Libánský, Ondřej; Vrána, Jiří; Pocedič, Jaromír; Mazúr, Petr; Kosek, Juraj

2017-12-01

The hydrogen evolution reaction is known as a parasitic reaction during the zinc electrodeposition from alkaline zincate solutions and is thus responsible for current efficiency losses during the electrolysis. Besides that, the rising hydrogen bubbles may cause an extra convection within a diffusion layer, which leads to an enhanced mass transport of zincate ions to an electrode surface. In this work, the mentioned phenomena were studied experimentally in a flow through electrolyzer and the obtained data were subsequently evaluated by mathematical models. The results prove the indisputable influence of the rising hydrogen bubbles on the additional mixing of the diffusion layer, which partially compensates the drop of the current efficiency of the zinc deposition at higher current flows. Moreover, the results show that the current density ratio (i.e., the ratio of an overall current density to a zinc limiting current density) is not suitable for the description of the zinc deposition, because the hydrogen evolution current density is always involved in the overall current density.

Sample preparation in alkaline media

International Nuclear Information System (INIS)

Nobrega, Joaquim A.; Santos, Mirian C.; Sousa, Rafael A. de; Cadore, Solange; Barnes, Ramon M.; Tatro, Mark

2006-01-01

The use of tetramethylammonium hydroxide, tertiary amines and strongly alkaline reagents for sample treatment involving extraction and digestion procedures is discussed in this review. The preparation of slurries is also discussed. Based on literature data, alkaline media offer a good alternative for sample preparation involving an appreciable group of analytes in different types of samples. These reagents are also successfully employed in tailored speciation procedures wherein there is a critical dependence on maintenance of chemical forms. The effects of these reagents on measurements performed using spectroanalytical techniques are discussed. Several undesirable effects on transport and atomization processes necessitate use of the method of standard additions to obtain accurate results. It is also evident that alkaline media can improve the performance of techniques such as inductively coupled plasma mass spectrometry and accessories, such as autosamplers coupled to graphite furnace atomic absorption spectrometers

Acidity and alkalinity in mine drainage: Theoretical considerations

Science.gov (United States)

Kirby, Carl S.; Cravotta,, Charles A.

2004-01-01

Acidity, net acidity, and net alkalinity are widely used parameters for the characterization of mine drainage, but these terms are not well defined and are often misunderstood. Incorrect interpretation of acidity, alkalinity, and derivative terms can lead to inadequate treatment design or poor regulatory decisions. We briefly explain derivations of theoretical expressions of three types of alkalinities (caustic, phenolphthalein, and total) and acidities (mineral, CO2, and total). Theoretically defined total alkalinity is closely analogous to measured alkalinity and presents few practical interpretation problems. Theoretically defined “CO2- acidity” is closely related to most standard titration methods used for mine drainage with an endpoint pH of 8.3, but it presents numerous interpretation problems, and it is unfortunately named because CO2 is intentionally driven off during titration of mine-drainage samples. Using the proton condition/massaction approach and employing graphs for visualization, we explore the concept of principal components and how to assign acidity contributions to solution species, including aqueous complexes, commonly found in mine drainage. We define a comprehensive theoretical definition of acidity in mine drainage on the basis of aqueous speciation at the sample pH and the capacity of these species to undergo hydrolysis to pH 8.3. This definition indicates the computed acidity in milligrams per liter (mg L-1 ) as CaCO3 (based on pH and analytical concentrations of dissolved FeIII , FeII , Mn, and Al in mg L-1 ): Aciditycomputed = 50. (10(3-pH) + 3.CFeIII/55.8 + 2.CFeII/55.8 + 2.CMn/54.9 + 3.CAl/27.0) underestimates contributions from HSO4 - and H+ , but overestimates the acidity due to Fe3+. These errors tend to approximately cancel each other. We demonstrate that “net alkalinity” is a valid mathematical construction based on theoretical definitions of alkalinity and acidity. We demonstrate that, for most mine-drainage solutions, a

Ion exchange behaviour of citrate and EDTA anions on strong and weak base organic ion exchangers

International Nuclear Information System (INIS)

Askarieh, M.M.; White, D.A.

1988-01-01

The exchange of citrate and EDTA ions with two strong base and two weak base exchangers is considered. Citrate and EDTA analysis for this work was performed using a colorimetric method developed here. The ions most selectively exchanged on the resins are H 2 cit - and H 2 EDTA 2- , though EDTA is generally less strongly sorbed on strong base resins. In contact with weak base resins, deprotonation of the resin occurs during ion exchange with a noticeable drop in solution pH. Although EDTA sorption can be reversed by nitric acid, citrate ions are significantly held on the resin at low pH. The exchange of citrate can be made reversible if bicarbonate is added to the initial solutions. Alkaline regeneration of exchangers loaded with EDTA proved to be very effective. (author)

Orbifolds and Exact Solutions of Strongly-Coupled Matrix Models

Science.gov (United States)

Córdova, Clay; Heidenreich, Ben; Popolitov, Alexandr; Shakirov, Shamil

2018-02-01

We find an exact solution to strongly-coupled matrix models with a single-trace monomial potential. Our solution yields closed form expressions for the partition function as well as averages of Schur functions. The results are fully factorized into a product of terms linear in the rank of the matrix and the parameters of the model. We extend our formulas to include both logarithmic and finite-difference deformations, thereby generalizing the celebrated Selberg and Kadell integrals. We conjecture a formula for correlators of two Schur functions in these models, and explain how our results follow from a general orbifold-like procedure that can be applied to any one-matrix model with a single-trace potential.

Analysis of longitudinal variations in North Pacific alkalinity

Science.gov (United States)

Fry, C.; Tyrrell, T.; Achterberg, E. P.

2016-02-01

Carbon measurements in the ocean lack the coverage of physical measurements, so approximate alkalinity is predicted where data is unavailable. Surface alkalinity in the North Pacific is poorly characterised by predictive algorithms. Understanding the processes affecting alkalinity in this area can improve the equations. We investigated the causes of regional variations in alkalinity using GLODAPv2. We tested different hypotheses for the causes of three longitudinal phenomena in surface ocean values of Alk*, a tracer of calcium carbonate cycling. These phenomena are: (a) an increase in Alk* from east to west at 50°N, (b) an increase in Alk* from west to east at 30°N, and (c) a lack of a strong increase in Alk* from west to east in the equatorial upwelling area. We found that the most likely cause of higher Alk* on the western side of the subpolar North Pacific (at 50°N) is that denser isopycnals with higher Alk* lie at shallower depths on the western side than the eastern side. At 30°N, the main cause of higher Alk* on the eastern side of the basin is upwelling along the continental shelf of southwestern North America. Along the equator, our analyses suggest that the absence of a strong east-west trend is because the more intense upwelling on the eastern side of the basin does not, under normal conditions, lead to strong elevation of Alk*. However, surface Alk* is more strongly elevated in the eastern Equatorial Pacific during negative phases of the El-Nino-Southern Oscillation, probably because the upwelled water comes from greater depth at these times.

Alkaline autoclave leaching of refractory uranium-thorium minerals

International Nuclear Information System (INIS)

Milani, S. A.; Sam, S.

2011-01-01

This paper deals with the study of an innovative method for processing the Oman placer ores by alkaline leaching in ball mill autoclaves, where grinding and leaching of the refractory minerals take place simultaneously. This was followed by the selective separation of thorium and uranium from lanthanides by autoclave leaching of the hydroxide cake with ammonium carbonate-bicarbonate solutions. The introduced method is based on the fact that thorium and uranium form soluble carbonate complexes with ammonium carbonate, while lanthanides form sparingly soluble double carbonates. It was found that a complete alkaline leaching of Oman placer ores (98.0 P ercent ) was attained at 150 and 175 d egree C within 2.5 and 2h, respectively. Oman placer ores leaching was intensified and accelerated in a ball mill autoclaves as a result of the grinding action of steel balls, removal of the hydroxide layer covering ores grains and the continuous contact of fresh ore grains with alkaline solution. The study of selective carbonate processing of hydroxide cake with ammonium carbonate-bicarbonate solutions on autoclave under pressure revealed that the complete thorium recovery (97.5 P ercent ) with uranium recovery (90.8 P ercent ) and their separation from the lanthanides were attained at 70-80 d egree C during l-2h. The extraction of lanthanides in carbonate solution was low and did not exceed 4.6 P ercent .

Effect of Alkaline Solution with Varying Mix Proportion on Geopolymer Mortar

Science.gov (United States)

Karuppuchamy, K.; Ananthkumar, M.; Raghavapriya, S. M.

2018-02-01

Cement production is attributed by emission of carbon dioxide which causes severe environmental impacts. This has led to the invention of special construction materials which can replace cement. On the other hand, these construction materials (like Fly ash, Metakaolin) also need to be inexpensive and should possess all the characteristics of cementitious materials. In this project, the effect of geopolymerization on the properties of the end product were studied with varying distillation of NaOH solution (10M, 12M and 15M) for different mix proportion (1:1, 1:2 and 1:3). Curing was done for 1 day at a temperature of 60°C and 80°C respectively. The densities, compressive strength, alkalinity, co-efficient of absorption were determined. As a result, the experiments showed the effect of factors such as mix proportion, curing temperature and curing day on the physical and mechanical properties such as mix proportion of the geopolymer concrete. Results of NaOH concentration of 12M concentration cured for 24 hours at 80°C and 60°C showed better mechanical performance than the rest of the concentrations.

The electrochemical behaviour of stainless steel AISI 304 in alkaline solutions with different pH in the presence of chlorides

International Nuclear Information System (INIS)

Freire, L.; Carmezim, M.J.; Ferreira, M.G.S.; Montemor, M.F.

2011-01-01

Highlights: → The passivation and passivation breakdown of AISI 304 in alkaline solutions with different pH was studied. → The electrochemical behaviour and the corrosion resistance in chloride environments were evaluated using d.c. potentiodynamic polarization and electrochemical impedance spectroscopy. → The results were modelled using a hierarchically distributed circuit and revealed a more susceptible surface at pH 9. → The passive film characterization was carried out by SEM and EDS analysis, revealing the existence of MnS inclusions and the increase of Cr/Fe ratio in the attacked areas, preferably the vicinity of those inclusions. - Abstract: Nowadays, stainless steel reinforcements appear as an effective solution to increase the durability of reinforced concrete structures exposed to very aggressive environments. AISI 304 is widely used for this purpose. Although the improved durability of reinforcing AISI 304, when compared to carbon steel, there is a high probability of pitting susceptibility in the presence of chlorides. Thus, the present work aims at studying the passivation and passivation breakdown of AISI 304 in alkaline solutions of different pH (pH from 13 to 9), simulating the interstitial concrete electrolyte. These solutions were contaminated with different concentrations of chloride ions (3% and 10%, as NaCl). The electrochemical behaviour was evaluated by d.c. potentiodynamic polarization and by electrochemical impedance spectroscopy (EIS). The morphological features and the changes observed in the surface composition were evaluated by Scanning Electron Microscopy (SEM) together with EDS chemical analysis. The results evidence that pH plays an important role in the evolution of the film resistance and charge transfer processes. Moreover, the effect is highly dependent upon the chloride content and immersion time.

Ion exchange of alkaline metals on the thin-layer zinc ferrocyanide

International Nuclear Information System (INIS)

Betenekov, N.D.; Buklanov, G.V.; Ipatova, E.G.; Korotkin, Yu.S.

1991-01-01

Basic regularities of interphase distribution in the system of thin-layer sorbent on the basis of mixed zinc ferrocyanide (FZ)-alkaline metal solution (Na, K, Rb, Cs, Fr) in the column chromatography made are studied. It is established that interphase distribution of microgram amounts of alkaline metals in the systems thin-layer FZ-NH 4 NO 3 electrolyte solutions is of ion-exchange character and subjected to of law effective mass. It is shown that FZ thin-layer material is applicable for effective chromatographic separation of alkaline metal trace amounts. An approach to the choice of a conditions of separate elution of Na, K, Rb, Cs, Fr in the column chromatography mode

Oxygen reduction at platinum nanoparticles supported on carbon cryogel in alkaline solution

Directory of Open Access Journals (Sweden)

N. R. ELEZOVIC

2007-07-01

Full Text Available The oxygen reduction reaction was investigated in 0.1 M NaOH solution, on a porous coated electrode formed of Pt particles supported on carbon cryogel. The Pt/C catalyst was characterized by the X-ray diffraction (XRD, transmission electron microscopy (TEM and cyclic voltammetry techniques. The results demonstrated a successful reduction of Pt to metallic form and homogenous Pt particle size distribution with a mean particle size of about 2.7 nm. The ORR kinetics was investigated by linear sweep polarization at a rotating disc electrode. The results showed the existence of two E – log j regions, usually referred to polycrystalline Pt in acid and alkaline solution. At low current densities (lcd, the Tafel slope was found to be close to –2.3RT/F, while at high current densities (hcd it was found to be close to –2×2.3RT/F. It is proposed that the main path in the ORR mechanism on Pt particles was the direct four-electron process, with the transfer of the first electron as the rate determining step. If the activities are expressed through the specific current densities, a small enhancement of the catalytic activity for Pt/C was observed compared to that of polycrystalline Pt. The effect of the Pt particle size on the electrocatalysis of oxygen reduction was ascribed to the predominant (111 facets of the platinum crystallites.

Corrosion of Cu-xZn alloys in slightly alkaline chloride solutions studied by stripping voltammetry and microanalysis.

Science.gov (United States)

Milosev, I; Minović, A

2001-01-01

The mechanism of corrosion of Cu-xZn alloys (x = 10-40 wt %) in slightly alkaline chloride solutions was investigated by analysing solid reaction products by energy dispersive X-ray analysis (EDS) and dissolved reaction products by differential anodic pulse stripping (DAPS) voltammetry. The corrosion process was studied under open circuit and under potentiostatic conditions at selected potentials. Pure metals were studied comparatively so that an interacting effect of particular metal components in the alloy could be determined. All four Cu-xZn alloys show an improved behaviour compared to pure metals. Under open-circuit condition both components dissolve simultaneously in the solution. With increasing immersion time the preferential, dissolution of zinc in the solution becomes pronounced. It is the highest for Cu-10Zn and the lowest for Cu-30Zn alloy. Under potentiostatic control the dissolution mechanism depends on the electrode potential and changes from exclusive dissolution of zinc to simultaneous dissolution of both components with preferential dissolution of zinc. The latter decreases, as the electrode potential becomes more positive.

Effects of aging on PuO{sub 2} . xH{sub 2}O particle size in alkaline solution

Energy Technology Data Exchange (ETDEWEB)

Delegard, C.H. [Pacific Northwest National Laboratory, Richland, WA (United States)

2013-08-01

Between 1944 and 1989, 54.5 metric tons of the United States' weapons-grade plutonium and an additional 12.9 metric tons of fuels-grade plutonium were produced in and separated from irradiated uranium metal fuel at the Hanford Site. Acidic high-activity wastes containing around 600 kg of plutonium were made alkaline and discharged to underground storage tanks from separations, isolation, and recycle processes to yield average plutonium concentration of about 0.003 g/L (or {proportional_to} 0.0002 wt. %) in the {proportional_to} 200 million liter tank waste volume. The plutonium is largely associated with low-solubility metal hydroxide/oxide sludges where its low concentration and intimate mixture with neutron-absorbing elements (e.g., iron) are credited in nuclear criticality safety. However, concerns have been expressed that plutonium, in the form of hydrated plutonium oxide, PuO{sub 2} . xH{sub 2}O, could undergo sufficient crystal growth through dissolution and reprecipitation in the alkaline tank waste to potentially become separable from neutron absorbing constituents by settling or sedimentation. Thermodynamic considerations and laboratory studies of systems chemically analogous to tank waste show that the plutonium, precipitated in the alkaline tank waste by neutralization from acid solution, probably entered as 2-5-nm PuO{sub 2} . xH{sub 2}O, crystallite particles that, because of the low concentration of the neutral Pu(IV) dissolved species and opposition from radiolytic processes, grow from that point at exceedingly slow rates. (orig.)

Fibrillation of Aspen by Alkaline Cold Pre-treatment and Vibration Milling

Directory of Open Access Journals (Sweden)

Kärt KÄRNER

2016-09-01

Full Text Available In this article an attempt to fibrillate aspen bleached chemi-thermo mechanical pulp (BCTMP fibre in an environmentally friendly way is reported. The effects of various NaOH, KOH, urea and ethanol aqueous solutions at lowered temperature were tested for pre-treatment. The pre-treatment was followed by vibration milling aiming to peel off outer cell wall layers and to fibrillate S2 layer of the aspen wood fibre. The effects of the treatments were evaluated by scanning electron microscopy (SEM. The results show that it is possible to fibrillate BCTMP aspen fibres by using alkaline aqueous solutions at low temperatures followed by a mechanical treatment. A strong dependence on fibrillation of cellulose on temperature, time and alkali concentration was established.DOI: http://dx.doi.org/10.5755/j01.ms.22.3.7412

Radiolysis of actinides and technetium in alkaline media

Energy Technology Data Exchange (ETDEWEB)

Delegard, C.H., Westinghouse Hanford

1996-07-10

The {gamma}-radiolysis of aerated alkaline aqueous solutions of Np(V), Np(VI), Pu(VI), Tc(IV), Tc(V), and TC(VII) was studied in the absence of additives and in the presence of CO{sub 3}{sup 2-}, NO{sub 3}{sup -}, NO{sub 2}{sup -}, EDTA, formate, and other organic compounds. The radiolytic reduction of Np(V), Np(VI), Pu(VI), and TC(VII) under different experimental conditions was examined in detail. The addition of EDTA, formate, and alcohols was found to considerably increase the radiation-chemical reduction yields. The formation of the Np(V) peroxo complex was observed in the {gamma}-radiolysis of alkaline aqueous solutions of Np (VI) in the presence of nitrate.

Treatment of chlorofluorocarbons in alcohol solutions by γ-irradiation

International Nuclear Information System (INIS)

Shimokawa, Toshinari; Nakagawa, Seiko; Sawai, Teruko

1995-01-01

A study was done on dechlorination of 1,1,2-trichloro-1,2,2-trifluoroethane (CFC113) in neutral and alkaline alcohol solutions by means of γ-irradiation. The dechlorination yield (G (Cl - )) was found to depend on the kind of alcohol used as solvents and the presence of hydroxide ion. The order of G (Cl - ) value in alkaline solution was isopropyl alcohol>> ethyl alcohol > methyl alcohol. It was suggested that the high yield obtained in alkaline isopropyl alcohol solution is explained by a chain process in dechlorination reaction. In case of alkaline isopropyl alcohol solution, CFC113 was dechlorinated to lower chlorinated ethane, and 1,1-dichloro-1,2,2-trifluoroetane was a main product. We have discussed on the chain dechlorination mechanism in alkaline isopropyl alcohol solution. (author)

Uranium(VI) retention by Ca-bentonite under (hyper)alkaline conditions

Energy Technology Data Exchange (ETDEWEB)

Philipp, Thimo; Schmeide, Katja [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Surface Processes

2017-06-01

The sorption behavior of U(VI) on Ca-bentonite was studied in saline, (hyper)alkaline solution via batch experiments. At pH 8.5-9.5 sorption is low in the presence of CO{sub 2} due to the formation of weakly sorbing uranyl carbonate species, which have been observed to dominate speciation up to pH 10 by time-resolved laser-induced fluorescence spectroscopy (TRLFS). In the pH region 10-12, U(VI) retention is almost complete. The retention can either be attributed to strongly sorbing uranyl hydroxo complexes or to a partial precipitation of uranium due to an altered solubility of U(VI) induced by ions leached out of the bentonite.

Hydrolysis of alkaline pretreated banana peel

Science.gov (United States)

Fatmawati, A.; Gunawan, K. Y.; Hadiwijaya, F. A.

2017-11-01

Banana peel is one of food wastes that are rich in carbohydrate. This shows its potential as fermentation substrate including bio-ethanol. This paper presented banana peel alkaline pretreatment and enzymatic hydrolysis. The pretreatment was intended to prepare banana peel in order to increase hydrolysis performance. The alkaline pretreatment used 10, 20, and 30% w/v NaOH solution and was done at 60, 70 and 80°C for 1 hour. The hydrolysis reaction was conducted using two commercial cellulose enzymes. The reaction time was varied for 3, 5, and 7 days. The best condition for pretreatment process was one conducted using 30% NaOH solution and at 80°C. This condition resulted in cellulose content of 90.27% and acid insoluble lignin content of 2.88%. Seven-day hydrolysis time had exhibited the highest reducing sugar concentration, which was7.2869 g/L.

Design and characterization of low-heat and low-alkalinity cements

International Nuclear Information System (INIS)

Codina, M.; Cau-dit-Coumes, C.; Le Bescop, P.; Verdier, J.; Ollivier, J.P.

2008-01-01

Investigations were carried out to formulate and characterize low-alkalinity and low-heat cements which would be compatible with an underground waste repository environment. Several systems comprising Portland cement, a pozzolan (silica fume or fly ash) and blastfurnace slag were compared. All blends were characterized by high amounts of additions, the Portland cement (PC) fraction ranging only from 20 to 60%. Cement hydration was studied using several techniques: X-ray Diffraction, TGA-DTA, calorimetry, pore solution extraction and microscopy. The most important result obtained with some ternary blends was the drop in the pore solution pH by more than one unit as compared with control samples elaborated with commercial cements. The alkali content (∼ 1 to 4 mmol/L) of the interstitial solution was also strongly reduced. The blends exhibited a low-heat output as required. Leaching tests carried out in pure water indicated a very slow decalcification of the samples. Several techniques such as optical microscopy, SEM/BSE, X-ray microanalysis or X-ray diffraction were compared to estimate the degraded thickness

Electrochemical behaviour of alkaline copper complexes

Indian Academy of Sciences (India)

Abstract. A search for non-cyanide plating baths for copper resulted in the development of alkaline copper complex baths containing trisodium citrate [TSC] and triethanolamine [TEA]. Voltammetric studies were carried out on platinum to understand the electrochemical behaviour of these complexes. In TSC solutions, the.

Theoretical studies on selectivity of dibenzo-18-crown-6-ether for alkaline earth divalent cations

Energy Technology Data Exchange (ETDEWEB)

Heo, Jiyoung [Sangmyung Univ., Seoul (Korea, Republic of)

2012-04-15

Crown ether is one of well-known host molecules and able to selectively sequester metal cation. We employed M06-2X density functional theory with IEFPCM and SMD continuum solvation models to study selectivity of dibenzo-18-crown-6-ether (DB18C6) for alkaline earth dications, Ba{sup 2+}, Sr{sup 2+}, Ca{sup 2+}, and Mg{sup 2+} in the gas phase and in aqueous solution. Mg{sup 2+} showed predominantly strong binding affinity in the gas phase because of strong polarization of CO bonds by cation. In aqueous solution, binding free energy differences became smaller among these dications. However, Mg{sup 2+} had the best binding, being incompatible with experimental observations in aqueous solution. The enthalpies of the dication exchange reaction between DB18C6 and water cluster molecules were computed as another estimation of selectivity in aqueous solution. These results also demonstrated that Mg{sup 2+} bound to DB18C6 better than Ba{sup 2+}. We speculated that the species determining selectivity in water could be 2:1 complexes of two DB18C6s and one dication.

Local strong solutions to the stochastic compressible Navier-Stokes system

Czech Academy of Sciences Publication Activity Database

Breit, D.; Feireisl, Eduard; Hofmanová, M.

2018-01-01

Roč. 43, č. 2 (2018), s. 313-345 ISSN 0360-5302 EU Projects: European Commission(XE) 320078 - MATHEF Institutional support: RVO:67985840 Keywords : compressible fluids * local strong solutions * Navier-Stokes system Subject RIV: BA - General Mathematics OBOR OECD: Pure mathematics Impact factor: 1.608, year: 2016 https://www.tandfonline.com/doi/full/10.1080/03605302.2018.1442476

Mega-solubility of quartz resulting from highly alkaline fluids produced by dissolved albite in H2O at deep crustal conditions

Science.gov (United States)

Makhluf, A. R.; Manning, C. E.

2017-12-01

Models of H2O-rich fluids equilibrated with rocks at high P and T fail to predict the high solubilities observed experimentally, chiefly because thermodynamic data for the most abundant solutes is lacking. We investigated the effects of dissolved albite (Ab) on the solubility of quartz (Qz) at 1.0 GPa and 675-900 °C using a piston-cylinder apparatus to quantify possible mineral buffering or enhancement effects. We found a very large enhancement effect on the solubility of Qz when dissolved in dilute aqueous Ab solutions. SiO2 concentrations are similar to Qz solubility in strongly alkaline KOH solutions. At the highest temperature of 900 °C, we found that the solubility of Qz in 1.0 molal Ab solution increases by of factor of 4.5 over that in pure H2O, which corresponds to 10.7 molal SiO2. The nearly identical solubility of Qz in KOH(aq) and Ab solutions of the same concentration, P, and T, strongly suggest that NaOH(aq) liberated from NaAlSi3O8 in H2O fluids effects SiO2 solubility in a similar manner to that of KOH(aq). The deprotonated silica dimer was found to be a key species responsible for the high solubility of Qz in KOH(aq) and is likely responsible for the high solubility of Qz in Ab solutions. While the binaries Qz-H2O, Ab-H2O, and Qz-Ab are well known at 1.0 GPa, little data exists on the ternary system. The new results help quantify the ternary relations in the Ab-Qz-H2O system, which can be used as a simple model for liquid-vapor immiscibility granitic magmas. In addition, these highly alkaline solute-rich aqueous fluids suggest a mechanism for Ab-Qz metasomatism in subduction zones, such as in the Catalina schist (Bebout and Barton 1993), which provides an alternative to high P-T magmas. Our results show that subduction zone and metasomatic fluids may be much more alkaline and have significantly higher dissolving power than previously thought.

In Vitro Determination of Bicarbonate Dosage to Alkalinize Local Anesthetics to Physiologic pH

Science.gov (United States)

1997-05-01

Lofgren’s contributions extend beyond the initial synthesis of Lidocaine ; his systematic study of an extensive assortment of compounds laid the foundation...maximizing time to precipitation formation. This descriptive study investigated the alkalinization of four local anesthetic solutions ( Lidocaine ... Lidocaine with epinephrine solutions for epidural administration (1986). While the benefits of alkalinization appear to be well established, the formation

Effect of Strongly Alkaline Electrolyzed Water on Silk Degumming and the Physical Properties of the Fibroin Fiber.

Directory of Open Access Journals (Sweden)

Ting-Ting Cao

Full Text Available Strongly alkaline electrolyzed water (SAEW was prepared by electrolysis of tap water in a laboratory-made water electrolyzer. The pH of stored SAEW was stable for more than one month. The hardness of the electrolyzed water was 30% lower and the Na(+ concentration was 18% higher than those of the tap water. Silkworm cocoon shells were boiled in pH 11.50 SAEW at a ratio of 1∶40∼80 (W/V for 20 min and the sericin layers around the silk fibroin fibers were removed completely. The tensile properties and thermal decomposition temperature of a single filament of silk fibroin obtained by the SAEW method were almost the same as those for the fiber obtained by the neutral soap, and much higher than those for the fiber obtained by Na2CO3 degumming. The results demonstrate that SAEW is an environmentally friendly and pollution-free silk degumming agent that allows highly efficient, low cost recovery of sericin.

Characterization Of Actinides In Simulated Alkaline Tank Waste Sludges And Leachates

International Nuclear Information System (INIS)

Nash, Kenneth L.

2008-01-01

In this project, both the fundamental chemistry of actinides in alkaline solutions (relevant to those present in Hanford-style waste storage tanks), and their dissolution from sludge simulants (and interactions with supernatants) have been investigated under representative sludge leaching procedures. The leaching protocols were designed to go beyond conventional alkaline sludge leaching limits, including the application of acidic leachants, oxidants and complexing agents. The simulant leaching studies confirm in most cases the basic premise that actinides will remain in the sludge during leaching with 2-3 M NaOH caustic leach solutions. However, they also confirm significant chances for increased mobility of actinides under oxidative leaching conditions. Thermodynamic data generated improves the general level of experiemental information available to predict actinide speciation in leach solutions. Additional information indicates that improved Al removal can be achieved with even dilute acid leaching and that acidic Al(NO3)3 solutions can be decontaminated of co-mobilized actinides using conventional separations methods. Both complexing agents and acidic leaching solutions have significant potential to improve the effectiveness of conventional alkaline leaching protocols. The prime objective of this program was to provide adequate insight into actinide behavior under these conditions to enable prudent decision making as tank waste treatment protocols develop.

CHARACTERIZATION OF ACTINIDES IN SIMULATED ALKALINE TANK WASTE SLUDGES AND LEACHATES

Energy Technology Data Exchange (ETDEWEB)

Nash, Kenneth L.

2008-11-20

In this project, both the fundamental chemistry of actinides in alkaline solutions (relevant to those present in Hanford-style waste storage tanks), and their dissolution from sludge simulants (and interactions with supernatants) have been investigated under representative sludge leaching procedures. The leaching protocols were designed to go beyond conventional alkaline sludge leaching limits, including the application of acidic leachants, oxidants and complexing agents. The simulant leaching studies confirm in most cases the basic premise that actinides will remain in the sludge during leaching with 2-3 M NaOH caustic leach solutions. However, they also confirm significant chances for increased mobility of actinides under oxidative leaching conditions. Thermodynamic data generated improves the general level of experiemental information available to predict actinide speciation in leach solutions. Additional information indicates that improved Al removal can be achieved with even dilute acid leaching and that acidic Al(NO3)3 solutions can be decontaminated of co-mobilized actinides using conventional separations methods. Both complexing agents and acidic leaching solutions have significant potential to improve the effectiveness of conventional alkaline leaching protocols. The prime objective of this program was to provide adequate insight into actinide behavior under these conditions to enable prudent decision making as tank waste treatment protocols develop.

Modification of the Selectivity Properties of Tubular Ceramic Membranes after Alkaline Treatment

Directory of Open Access Journals (Sweden)

Patrick Dutournié

2017-11-01

Full Text Available This work focuses on the selectivity modification of ceramic membranes after a mild alkaline treatment. Filtration of pure salt-water solutions was carried out with commercial titania membranes before and after the treatment. After treatment, the rejection of NaF significantly decreased, while the rejection of NaCl and NaBr increased. Additionally, NaI and Na2SO4 remained close to zero. Pore size and electrical charge being almost unchanged, only significant modifications in the dielectric effects can explain this modification of selectivity. Therefore, the surface chemistry and the interaction (nature and magnitude with the solvent and with the species present in the solution appear to be modified by the alkaline treatment. This trend is also illustrated by discussing the electric and the dielectric properties that were numerically identified before and after treatment. The alkaline treatment significantly decreased the apparent dielectric constant of NaCl-water solution in the pore, highlighting the rejection of sodium chloride. Contrariwise, the modification of the surface chemistry increased the apparent dielectric constant of NaF-water solution by promoting fluoride transmission.

Ultrastable α phase nickel hydroxide as energy storage materials for alkaline secondary batteries

Science.gov (United States)

Huang, Haili; Guo, Yinjian; Cheng, Yuanhui

2018-03-01

α Phase nickel hydroxide (α-Ni(OH)2) has higher theoretical capacity than that of commercial β phase Ni(OH)2. But the low stability inhibits its wide application in alkaline rechargeable batteries. Here, we propose a totally new idea to stabilize α phase Ni(OH)2 by introducing large organic molecule into the interlayer spacing together with doping multivalent cobalt into the layered Ni(OH)2 host. Ethylene glycol is served as neutral stabilizer in the interlayer spacing. Nickel is substituted by cobalt to increase the electrostatic attraction between layered Ni(OH)2 host and anion ions in the interlayer spacing. Polyethylene glycol (PEG-200) is utilized to design a three-dimensional network structure. This prepared α-Ni(OH)2-20 exhibits specific capacity as high as 334 mAh g-1and good structural stability even after immersing into strong alkaline zincate solution for 20 days. Ni(OH)2 electrode with a specific capacity of 35 mAh cm-2 is fabricated and used as positive electrode in zinc-nickel single flow batteries, which also shows good cycling stability. This result can provide an important guideline for the rational design and preparation of highly active and stable α phase Ni(OH)2 for alkaline secondary battery.

Pollution control and resource reuse for alkaline hydrometallurgy of amphoteric metal hazardous wastes

CERN Document Server

Youcai, Zhao

2017-01-01

This book provides a comprehensive description of alkaline hydrometallurgy of amphoteric metal hazardous wastes. Topics focus on leaching of zinc and lead hazardous wastes, purification of leach solution of zinc and lead, electrowinning of zinc and lead from purified alkaline solutions, chemical reactions taking place in the production flowsheets, thermodynamic and spent electrolyte regeneration, alkaline hydrometallurgy of low-grade smithsonite ores, recovery of molybdenum and tungsten using ion flotation and solvent extraction processes and their application in chemical synthesis of Nb and Ta inorganic compounds, and industrial scale production of 1500-2000 t/a zinc powder using alkaline leaching–electrowinning processes. Processes described are cost-effective, generate lesser secondary pollutants, and have been applied widely in China. Readers that will find the book appealing include solid waste engineers, environmental managers, technicians, recycling coordinators, government officials, undergraduates ...

Ammonium carbonate and/or bicarbonate plus alkaline chlorate oxidant for recovery of uranium values

International Nuclear Information System (INIS)

Stapp, P.R.

1983-01-01

In accordance with the present invention, uranium values are extracted from materials containing uranium in valence states lower than its hexavalent state by contacting the materials containing uranium with an aqueous alkaline leach solution containing an alkaline chlorate in an amount sufficient to oxidize at least a portion of the uranium in valence states lower than its hexavalent state to its hexavalent state. In a further embodiment of the present invention, the alkaline leach solution is an aqueous solution of a carbonate selected from the group consisting of ammonium carbonate, ammonium bicarbonate and mixtures thereof. In yet another embodiment of the present invention, at least one catalytic compound of a metal selected from the group consisting of copper, cobalt, iron, nickel, chromium and mixtures thereof adapted to assure the presence of the ionic species Cu ++ , Co ++ , Fe +++ , Ni ++ , Cr +++ and mixtures thereof, respectively, during the contacting of the material containing uranium with the alkaline leach solution and in an amount sufficient to catalyze the oxidation of at least a portion of the uranium in its lower valence states to its hexavalent state, is present

Solutions to the strong-CP problem in a world with gravity

International Nuclear Information System (INIS)

Holman, R.; Watkins, R.; Widrow, L.M.; Toronto Univ., ON

1992-01-01

We examine various solutions of the strong-CP problem to determine their sensitivity to possible violations of global symmetries by Plauck scale physics. While some solutions remain viable even in the face of such effects. Violations of the Peccei-Quinn (PQ) symmetry by non-renormalizable operators of dimension less than 10 will generally shift the value of bar θ to values inconsistent with the experimental bound bar θ approx-lt 10 - 9. We show that it is possible to construct axion models where gauge symmetries protect PQ symmetry to the requisite level

Extraction process of U from its ores using solutions of alkaline earth carbonates and bicarbonates in presence of carbon dioxide

International Nuclear Information System (INIS)

Floreancig, Antoine; Schuffenecker, Robert.

1976-01-01

A process is described for extracting uranium from its ores, either directly in the ore deposit or after such ore bodies have been taken from the ground, comprising an oxidation-leaching stage followed by a recovery stage. The characteristic of this process is that in the leaching process, carbonate and bicarbonate solutions of an alkaline-earth metal are used under a pressure of carbon dioxide between zero and 60 bars and at a temperature of zero to 100 0 C [fr

Net alkalinity and net acidity 2: Practical considerations

Science.gov (United States)

Kirby, C.S.; Cravotta, C.A.

2005-01-01

The pH, alkalinity, and acidity of mine drainage and associated waters can be misinterpreted because of the chemical instability of samples and possible misunderstandings of standard analytical method results. Synthetic and field samples of mine drainage having various initial pH values and concentrations of dissolved metals and alkalinity were titrated by several methods, and the results were compared to alkalinity and acidity calculated based on dissolved solutes. The pH, alkalinity, and acidity were compared between fresh, unoxidized and aged, oxidized samples. Data for Pennsylvania coal mine drainage indicates that the pH of fresh samples was predominantly acidic (pH 2.5-4) or near neutral (pH 6-7); ??? 25% of the samples had pH values between 5 and 6. Following oxidation, no samples had pH values between 5 and 6. The Standard Method Alkalinity titration is constrained to yield values >0. Most calculated and measured alkalinities for samples with positive alkalinities were in close agreement. However, for low-pH samples, the calculated alkalinity can be negative due to negative contributions by dissolved metals that may oxidize and hydrolyze. The Standard Method hot peroxide treatment titration for acidity determination (Hot Acidity) accurately indicates the potential for pH to decrease to acidic values after complete degassing of CO2 and oxidation of Fe and Mn, and it indicates either the excess alkalinity or that required for neutralization of the sample. The Hot Acidity directly measures net acidity (= -net alkalinity). Samples that had near-neutral pH after oxidation had negative Hot Acidity; samples that had pH mine drainage treatment can lead to systems with insufficient Alkalinity to neutralize metal and H+ acidity and is not recommended. The use of net alkalinity = -Hot Acidity titration is recommended for the planning of mine drainage treatment. The use of net alkalinity = (Alkalinitymeasured - Aciditycalculated) is recommended with some cautions

Ocean Acidification: Coccolithophore's Light Controlled Effect on Alkalinity

Science.gov (United States)

Dobbins, W.

2015-12-01

Coccolithophorids, which play a significant role in the flux of calcite and organic carbon from the photic region to deeper pelagic and benthic zones, are potentially far more useful than siliceous phytoplankton for ocean fertilization projects designed to sequester CO2. However, the production of H+ ions during calcification (HCO3 + Ca+ —> CaCO3 + H+) has resulted in localized acidification around coccolithophore blooms. It has been hypothesized that under the correct light conditions photosynthesis could proceed at a rate such that CO2 is removed in amounts equimolar or greater than the H+ produced by calcification, allowing stable or increasing alkalinity despite ongoing calcification. Previously, this effect had not been demonstrated under laboratory conditions. Fifteen Emiliania huxleyi cultures were separated into equal groups with each receiving: 0, 6, 12, 18, or 24 hours of light each day for 24 days. Daily pH, cell density, and temperature measurements revealed a strong positive correlation between light exposure and pH, and no significant decline in pH in any of the cultures. Alkalinity increases were temperature independent and not strongly correlated with cell density, implying photosynthetic removal of carbon dioxide as the root cause. The average pH across living cultures increased from 7.9 to 8.3 over the first week and changed little for the reminder of the 24-day period. The results demonstrate coccolithophorids can increase alkalinity across a broad range of cell densities, despite the acidification inherent to the calcification process. If the light-alkalinity effect reported here proves scalable to larger cultures, Emiliania huxleyi are a strong candidate for carbon sequestration via targeted ocean fertilization.

Evaluation of electrolytic alkaline cleaners by evaporative-rate analysis

International Nuclear Information System (INIS)

Hamilton, C.B.

1975-01-01

A method has been developed by which electrolytic alkaline cleaners used in large volumes in steel mills can be evaluated for their ability to clean rolling oil from steel strip without the necessity of large-scale mill trials. The method is evaporative-rate analysis, which can be used to determine the relative amount of residual oil on steel strip after cleaning. The procedure consists in placing a droplet of a solution of a volatile, radioactive, carbon-14 tagged organic compound dissolved in a more volatile solvent, on the surface of the metal, where it forms a ternary solution with any oil on the surface. The amount of oil in this ternary solution affects the rate of evaporation of the tagged compound. The rate of evaporation, monitored by a Geiger-Mueller detector, is a measure of the cleanliness of the surface. A number of commercial alkaline cleaners, both solids and liquids, were evaluated over a range of concentrations. Results indicated that the effectiveness of commercial alkaline cleaners varies greatly, and is a function of the cleaner concentration, cleaner composition, and polarity of cleaning. The presence of antifoaming agents also affects cleaning ability. The results of this study indicate that evaporative-rate analysis is a rapid and effective method for evaluating cleaners

Oxidation of propionic acid-3-14C with alkaline permanganate

International Nuclear Information System (INIS)

Zielinski, M.

1981-01-01

The mechanism of oxidation of propionic acid with permanganate in alkaline medium was reinvestigated using methyl- 14 C labelled propionate. The preferential rupture of the αC-βC bond in propionate in highly concentrated alkaline solutions of NaOH (and KOH) was confirmed and the appearance of 14 C-labelled oxalate explained by the formation of the symmetrical intermediate which decomposes in two different modes. (author)

Alkaline erosion of CR 39 polymer surfaces

International Nuclear Information System (INIS)

Faiman, Laurence

2009-01-01

We have investigated the mechanism of erosion of CR 39 polymer in alkaline environments. We observed the kinetics of absorption of water and methanol into both unirradiated and γ-irradiated samples. We use a capillary model to interpret our results. We etched our samples in both KOH solutions, and KOH solutions doped with methanol. Etch rate was desensitizing to γ-irradiation when KOH concentration approached saturation, but KOH solutions doped with methanol were not desensitizing, unlike with nuclear tracks. We account for this difference

Actinide-Aluminate Speciation in Alkaline Radioactive Waste

International Nuclear Information System (INIS)

Clark, David L.; Fedosseev, Alexander M.

2001-01-01

Investigation of behavior of actinides in alkaline media containing AL(III) showed that no aluminate complexes of actinides in oxidation states (IIII-VIII) were formed in alkaline solutions. At alkaline precipitation IPH (10-14) of actinides in presence of AL(III) formation of aluminate compounds is not observed. However, in precipitates contained actinides (IIV)<(VI), and to a lesser degree actinides (III), some interference of components takes place that is reflected in change of solid phase properties in comparison with pure components or their mechanical mixture. The interference decreases with rise of precipitation PH and at PH 14 is exhibited very feebly. In the case of NP(VII) the individual compound with AL(III) is obtained, however it is not aluminate of neptunium(VII), but neptunate of aluminium(III) similar to neptunates of other metals obtained earlier

Production of ultrafine zinc powder from wastes containing zinc by electrowinning in alkaline solution

Directory of Open Access Journals (Sweden)

Zhao Youcai

2013-12-01

Full Text Available Production of ultrafine zinc powder from industrial wastes by electrowinning in alkaline solution was studied. Stainless steel and magnesium electrodes were used as anode and cathode, respectively. Morphology, size distribution and composition of the Zn particles were characterized by Scanning Electron Microscopy, Laser Particle Size Analyzer, and Inductive Coupled Plasma Emission Spectrometer. The required composition of the electrolyte for ultrafine particles was found to be 25-35 g/L Zn, 200-220 g/L NaOH and 20-40 mg/L Pb. The optimal conditions were a current density of 1000-1200 A/m² and an electrolyte temperature of 30-40 °C. The results indicated that the lead additive exerted a beneficial effect on the refining of the particles, by increasing the cathodic polarization. Through this study, ultrafine zinc powder with a size distribution of around 10 μm could be produced, and considerably high current efficiencies (97-99 % were obtained.

Anodizing of magnesium alloy AZ31 in alkaline solutions with silicate under continuous sparking

International Nuclear Information System (INIS)

Chai Liyuan; Yu Xia; Yang Zhihui; Wang Yunyan; Okido, Masazumi

2008-01-01

Anodization is a useful technique for forming protective films on magnesium alloys and improves its corrosion resistance. Based on the alkaline electrolyte solution with primary oxysalt developed previously, the optimum secondary oxysalt was selected by comparing the anti-corrosion property of anodic film. The structure, component and surface morphology of anodic film and cross-section were analyzed using energy dispersion spectrometer (EDS), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The corrosion process was detected by electrochemical impedance spectroscopy (EIS). The results showed that secondary oxysalt addition resulted in different anodizing processes, sparking or non-sparking. Sodium silicate was the most favorable additive of electrolyte, in which anodic film with the strongest corrosion resistance was obtained. The effects of process parameters, such as silicate concentration, applied current density and temperature, were also investigated. High temperature did not improve anti-property of anodic film, while applying high current density resulted in more porous surface of film

Solution of the strong CP problem in models with scalars

International Nuclear Information System (INIS)

Dimopoulos, S.

1978-01-01

A possible solution to the strong CP problem is pointed out within the context of a Weinberg--Salam model with two Higgs fields coupled in a Peccei--Quinn symmetric fashion. This is done by extending the colour group to a bigger simple group which is broken at some very high energy. The model contains a heavy axion. No old or new U(1) problem re-emerges. 31 references

Planck-scale physics and solutions to the strong CP-problem without axion

International Nuclear Information System (INIS)

Berezhiani, Z.G.; Mohapatra, R.N.; Senjanovic, G.

1992-12-01

We analyse the impact of quantum gravity on the possible solutions to the strong CP problem which utilize the spontaneously broken discrete symmetries, such as parity and time reversal invariance. We find that the stability of the solution under Planck scale effects provides an upper limit on the scale Λ of relevant symmetry breaking. This result is mode dependent and the bound is most restrictive for the seesaw type models of fermion masses, with Λ 6 GeV. (author). 32 refs

Dark matter and dark energy from the solution of the strong CP problem.

Science.gov (United States)

Mainini, Roberto; Bonometto, Silvio A

2004-09-17

The Peccei-Quinn (PQ) solution of the strong CP problem requires the existence of axions, which are viable candidates for dark matter. If the Nambu-Goldstone potential of the PQ model is replaced by a potential V(|Phi|) admitting a tracker solution, the scalar field |Phi| can account for dark energy, while the phase of Phi yields axion dark matter. If V is a supergravity (SUGRA) potential, the model essentially depends on a single parameter, the energy scale Lambda. Once we set Lambda approximately equal to 10(10) GeV at the quark-hadron transition, |Phi| naturally passes through values suitable to solve the strong CP problem, later growing to values providing fair amounts of dark matter and dark energy.

Distributions of 14 elements on 63 absorbers from three simulant solutions (acid-dissolved sludge, acidified supernate, and alkaline supernate) for Hanford HLW Tank 102-SY

International Nuclear Information System (INIS)

Marsh, S.F.; Svitra, Z.V.; Bowen, S.M.

1994-08-01

As part of the Hanford Tank Waste Remediation System program at Los Alamos, we evaluated 63 commercially available or experimental absorber materials for their ability to remove hazardous components from high-level waste (HLW). These absorbers included cation and anion exchange resins, inorganic exchangers, composite absorbers, and a series of liquid extractants sorbed on porous support-beads. We tested these absorbers with three solutions prepared to simulate acid-dissolved sludge (pH 0.6), acidified supernate (pH 3.5), and alkaline supernate (pH 13.9) from underground storage tank 102-SY at the Hanford Reservation near Richland, Washington. To these simulants we added the appropriate radionuclides and used gamma spectrometry to measure fission products (Ce, Cs, Sr, Tc, and Y), actinides (U, Pu, and Am), and matrix elements (Cr, Co, Fe, Mn, Zn, and Zr). For each of more than 2500 element/absorber/solution combinations, we measured distribution coefficients for dynamic contact periods of 30 min, 2 h, and 6 h to obtain information about sorption kinetics. Because we measured the sorption of many different elements, the tabulated results indicate those elements most likely to interfere with the sorption of elements of greater interest. On the basis of nearly 7500 measured distribution coefficients, we determined that many of these absorbers appear suitable for processing HLW. This study supersedes the previous version of LA-12654, in which results attributed to a solution identified as an alkaline supernate simulant were misleading because that solution contained insufficient hydroxide

Explicit and exact solutions for a generalized long-short wave resonance equations with strong nonlinear term

International Nuclear Information System (INIS)

Shang Yadong

2005-01-01

In this paper, the evolution equations with strong nonlinear term describing the resonance interaction between the long wave and the short wave are studied. Firstly, based on the qualitative theory and bifurcation theory of planar dynamical systems, all of the explicit and exact solutions of solitary waves are obtained by qualitative seeking the homoclinic and heteroclinic orbits for a class of Lienard equations. Then the singular travelling wave solutions, periodic travelling wave solutions of triangle functions type are also obtained on the basis of the relationships between the hyperbolic functions and that between the hyperbolic functions with the triangle functions. The varieties of structure of exact solutions of the generalized long-short wave equation with strong nonlinear term are illustrated. The methods presented here also suitable for obtaining exact solutions of nonlinear wave equations in multidimensions

Oxidative degradation of Boltysh shale by alkaline potassium permanganate

Energy Technology Data Exchange (ETDEWEB)

Pobul, I Ya; Fomina, A S

1974-01-01

This reaction proceeded in stages at 47 to 48/sup 0/C with a 3 percent solution of potassium permanganate in a 1 percent alkaline solution. The products were separated into groups and identified by gas-liquid chromatography. Small amounts of monocarboxylic acids were identified, with normal and branched chains, from acetic to lauric acid. Dicarboxylic acids were mainly of normal structure, or methyl substituted, from succinic to hexadecanedicarboxylic acid. No tricarboxylic acids were detected. For products of primary oxidation insoluble in acid media, a high content of C/sub 10/-C/sub 16/ acids was characteristic, and for the final degree of oxidation C/sub 11/-C/sub 18/ acids. The organic portion of shale consists of structural units, differing in mass and in stability to alkaline permanganate.

Nonelectrolyte NRTL-NRF model to study thermodynamics of strong and weak electrolyte solutions

Energy Technology Data Exchange (ETDEWEB)

Haghtalab, Ali, E-mail: haghtala@modares.ac.i [Department of Chemical Engineering, Tarbiat Modares University, P.O. Box 14115-143, Tehran (Iran, Islamic Republic of); Shojaeian, Abolfazl; Mazloumi, Seyed Hossein [Department of Chemical Engineering, Tarbiat Modares University, P.O. Box 14115-143, Tehran (Iran, Islamic Republic of)

2011-03-15

An electrolyte activity coefficient model is proposed by combining non-electrolyte NRTL-NRF local composition model and Pitzer-Debye-Hueckel equation as short-range and long-range contributions, respectively. With two adjustable parameters per each electrolyte, the present model is applied to correlation of the mean activity coefficients of more than 150 strong aqueous electrolyte solutions at 298.15 K. Also the results of the present model are compared with the other local composition models such as electrolyte-NRTL, electrolyte-NRTL-NRF and electrolyte-Wilson-NRF models. Moreover, the present model is used for prediction of the osmotic coefficient of several aqueous binary electrolytes systems at 298.15 K. Also the present activity coefficient model is adopted for representation of nonideality of the acid gases, as weak gas electrolytes, soluble in alkanolamine solutions. The model is applied for calculation of solubility and heat of absorption (enthalpy of solution) of acid gas in the two {l_brace}(H{sub 2}O + MDEA + CO{sub 2}) and (H{sub 2}O + MDEA + H{sub 2}S){r_brace} systems at different conditions. The results demonstrate that the present model can be successfully applied to study thermodynamic properties of both strong and weak electrolyte solutions.

Purification of alkaline solutions and wastes from actinides and technetium by coprecipitation with some carriers using the method of appearing reagents: Final Report

International Nuclear Information System (INIS)

Peretrukhin, V.F.; Silin, V.I.; Kareta, A.V.; Gelis, A.V.; Shilov, V.P.; German, K.E.; Firsova, E.V.; Maslennikov, A.G.; Trushina, V.E.

1998-09-01

The coprecipitation of transuranium elements (TRU) and technetium from alkaline solutions and from simulants of Hanford Site tank wastes has been studied in reducing and oxidizing conditions on uranium(IV,VI) hydroxocompounds, tetraalkylammonium perrhenate and perchlorate, and on hydroxides of Fe(III), Co(III), Mn(II), and Cr(III) using the method of appearing reagents (MAR). Coprecipitations in alkaline solution have been shown to give high decontamination factors (DF) at low content of carrier and in the presence of high salt concentrations. Uranium(IV) hydroxide in concentrations higher than 3 x 10 -3 M coprecipitates Pu and Cm in any oxidation state from 0.2 to 4 M NaOH with DFs of 110 to 1000 and Np and Tc with DFs of 51 to 176. Technetium (VII) coprecipitates with (5 to 8) x 10 -4 M tetrabutylammonium (TBA) perrhenate in 0.01 to 0.02 M TBA hydroxide from 0.5 to 1.5 M NaOH to give DFs of 150 to 200. Coprecipitations of Np and Pu with Co(OH) 3 , Fe(OH) 3 , Cr(OH) 3 , and Mn(OH) 2 obtained by the MAR from precursors in the range from pH 10.5 to 0.4 M NaOH give DFs from 80 to 400

Improved hydrogen generation from alkaline NaBH{sub 4} solution using cobalt catalysts supported on modified activated carbon

Energy Technology Data Exchange (ETDEWEB)

Xu, Dongyan; Guo, Qingjie; Yue, Xuehai [College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China); Dai, Ping [College of Electromechanical Engineering, Qingdao University of Science and Technology, Qingdao 266061 (China)

2008-12-15

Hydrogen production from alkaline sodium borohydride (NaBH{sub 4}) solution via hydrolysis process over activated carbon supported cobalt catalysts is studied. Activated carbons are used in their original form and after liquid phase oxidation with HNO{sub 3}. The changes in surface functional groups of the activated carbon are detected by FTIR spectroscopy. The effects of HNO{sub 3} oxidation on the properties of the activated carbon and the resulting catalyst performance are investigated. FTIR analysis reveals that the oxidative treatment leads to the formation of various functional groups on the surface of the activated carbon. Cobalt catalysts supported on the modified activated carbon are found to exhibit higher activity and stability. (author)

Properties of altered soils by alkaline solution: contribution in the performance evaluation of repositories; Propriedades de solos alterados por solucao alcalina: contribuicao na avaliacao de desempenho de repositorios

Energy Technology Data Exchange (ETDEWEB)

Calabria, Jaqueline Alves de Almeida

2015-07-01

very low for all evaluated samples (less than 20% after 10 days of equilibrium), being the best performance one, the nitosoil sample whose K{sub d} values varied from 11.78 to 63.05 mL.g{sup -1}. In a subsequent step, the clay soil, was submitted to the alkaline solution interaction, in order to investigate possible alterations on the sorption properties and hydraulic conductivity of this soil. Using the sorption parameters, obtained from data fitted isotherms, the retardation factor, R, was estimated for the samples before and after the interaction. It was demonstrated that the alkaline alteration promotes damages to sorption properties of Cs, once the R became significantly smaller (about 1000 times) after the interaction. The hydraulic conductivity in turn increased slightly (3,91x10{sup -8} cm.s{sup -1} to 5,08 x 10{sup -8} cm.s{sup -1}). It was concluded that these changes were due, mainly, to the dissolution of minerals present in the clay soil (kaolinite and quartz), associated with the incorporation of K and Ca from the alkaline solution, resulting, probably, in the formation of hydrated calcium silicate phases. Additionally, the effects of alkaline solution on the properties of a commercial bentonite were studied. Contrary to the clay soil, it was observed a gain in the sorption characteristics, with K{sub d} (Cs) increasing from 760.05 mL.g{sup -1}to 1311.80 mL.g{sup -1}and Q{sub max} from 36.32 mg.g{sup -1}to 52.13 mg.g{sup -1}, with the corresponding increase in the retardation coefficient, R. The dissolution of the clay minerals from the initial sample and the incorporation of Mg, K e Ca coming from the alkaline solution, generating smectite of different kinds, were considered as the main mineralogical changes responsible for the modifications in sorption parameters. The different behavior between the two evaluated samples, soil and bentonite, confirms that the nature and extension of changes observed, when mineral samples interact with alkaline solution

Bentonite reactivity in alkaline solutions: results of the Cyprus natural analogue project (CNAP)

International Nuclear Information System (INIS)

Alexander, W.R.; Milodowski, A.E.; Pitty, A.F.; Hardie, S.M.L.; Korkeakoski, P.; Norris, S.; Puigdomenech, I.; Sellin, P.; Rigas, M.

2012-01-01

Document available in extended abstract form only. Bentonite is one of the most safety-critical components of the engineered barrier system in the disposal concepts developed for many types of radioactive waste. Bentonite is used due to its favourable properties (including plasticity, swelling capacity, colloid filtration, low hydraulic conductivity, high retardation of key radionuclides) and its stability in relevant geological environments. However, bentonite is unstable under alkaline conditions and, due to the fact that cementitious materials react with groundwater to produce initial leachates with pH >13 (later falling to around pH 12.5), this has driven recent interest in low alkali cements, because the pH of the leachate is somewhat lower than standard OPC (Ordinary Portland Cement), lying around pH 10-11. It is hoped that this lower pH will reduce bentonite reaction, so allowing the use of low alkali cements in close proximity with bentonite. Assuring the long-term stability of bentonite in contact with such alkaline fluids under conditions representative of a deep geological repository requires complementary laboratory, modelling and in situ studies. In particular, to build a robust safety case, it is important to have supporting natural analogue data to confirm understanding - and validate models - of the likely long-term performance of bentonite. As a result of a review of the available literature and recent geological investigations by the authors, several sites in Cyprus were selected as particularly promising for this purpose. All alkaline groundwaters studied so far in Cyprus originate from ophiolite host rocks which are wide-spread across the island. The alkaline pH values (generally between pH 10 and 11, but a maximum of 12 has been observed) reported in the groundwaters are a product of the serpentinization of the ophiolites. The presence of bentonite and other clay-rich rocks in close proximity to the natural alkaline groundwaters permits the

A solution of the strong CP problem in models with scalars

International Nuclear Information System (INIS)

Dimopoulos, S.

1979-01-01

A possible solution to the strong CP problem within the context of a Weinberg-Salam model with two Higgs fields coupled in a Peccei-Quinn symmetric fashion is pointed out. This is done by extending the colour group to a bigger simple group which is broken at some very high energy. The model contains a heavy axion. No old or new U(1) problem re-emerges. (Auth.)

When can ocean acidification impacts be detected from decadal alkalinity measurements?

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Carter, B. R.; Frölicher, T. L.; Dunne, J. P.; Rodgers, K. B.; Slater, R. D.; Sarmiento, J. L.

2016-04-01

We use a large initial condition suite of simulations (30 runs) with an Earth system model to assess the detectability of biogeochemical impacts of ocean acidification (OA) on the marine alkalinity distribution from decadally repeated hydrographic measurements such as those produced by the Global Ship-Based Hydrographic Investigations Program (GO-SHIP). Detection of these impacts is complicated by alkalinity changes from variability and long-term trends in freshwater and organic matter cycling and ocean circulation. In our ensemble simulation, variability in freshwater cycling generates large changes in alkalinity that obscure the changes of interest and prevent the attribution of observed alkalinity redistribution to OA. These complications from freshwater cycling can be mostly avoided through salinity normalization of alkalinity. With the salinity-normalized alkalinity, modeled OA impacts are broadly detectable in the surface of the subtropical gyres by 2030. Discrepancies between this finding and the finding of an earlier analysis suggest that these estimates are strongly sensitive to the patterns of calcium carbonate export simulated by the model. OA impacts are detectable later in the subpolar and equatorial regions due to slower responses of alkalinity to OA in these regions and greater seasonal equatorial alkalinity variability. OA impacts are detectable later at depth despite lower variability due to smaller rates of change and consistent measurement uncertainty.

Net alkalinity and net acidity 1: Theoretical considerations

International Nuclear Information System (INIS)

Kirby, Carl S.; Cravotta, Charles A.

2005-01-01

Net acidity and net alkalinity are widely used, poorly defined, and commonly misunderstood parameters for the characterization of mine drainage. The authors explain theoretical expressions of 3 types of alkalinity (caustic, phenolphthalein, and total) and acidity (mineral, CO 2 , and total). Except for rarely-invoked negative alkalinity, theoretically defined total alkalinity is closely analogous to measured alkalinity and presents few practical interpretation problems. Theoretically defined 'CO 2 -acidity' is closely related to most standard titration methods with an endpoint pH of 8.3 used for determining acidity in mine drainage, but it is unfortunately named because CO 2 is intentionally driven off during titration of mine-drainage samples. Using the proton condition/mass-action approach and employing graphs to illustrate speciation with changes in pH, the authors explore the concept of principal components and how to assign acidity contributions to aqueous species commonly present in mine drainage. Acidity is defined in mine drainage based on aqueous speciation at the sample pH and on the capacity of these species to undergo hydrolysis to pH 8.3. Application of this definition shows that the computed acidity in mgL -1 as CaCO 3 (based on pH and analytical concentrations of dissolved Fe II , Fe III , Mn, and Al in mgL -1 ):acidity calculated =50{1000(10 -pH )+[2(Fe II )+3(Fe III )]/56+2(Mn) /55+3(Al)/27}underestimates contributions from HSO 4 - and H + , but overestimates the acidity due to Fe 3+ and Al 3+ . However, these errors tend to approximately cancel each other. It is demonstrated that 'net alkalinity' is a valid mathematical construction based on theoretical definitions of alkalinity and acidity. Further, it is shown that, for most mine-drainage solutions, a useful net alkalinity value can be derived from: (1) alkalinity and acidity values based on aqueous speciation (2) measured alkalinity minus calculated acidity, or (3) taking the negative of the

Net alkalinity and net acidity 1: Theoretical considerations

Science.gov (United States)

Kirby, C.S.; Cravotta, C.A.

2005-01-01

Net acidity and net alkalinity are widely used, poorly defined, and commonly misunderstood parameters for the characterization of mine drainage. The authors explain theoretical expressions of 3 types of alkalinity (caustic, phenolphthalein, and total) and acidity (mineral, CO2, and total). Except for rarely-invoked negative alkalinity, theoretically defined total alkalinity is closely analogous to measured alkalinity and presents few practical interpretation problems. Theoretically defined "CO 2-acidity" is closely related to most standard titration methods with an endpoint pH of 8.3 used for determining acidity in mine drainage, but it is unfortunately named because CO2 is intentionally driven off during titration of mine-drainage samples. Using the proton condition/mass- action approach and employing graphs to illustrate speciation with changes in pH, the authors explore the concept of principal components and how to assign acidity contributions to aqueous species commonly present in mine drainage. Acidity is defined in mine drainage based on aqueous speciation at the sample pH and on the capacity of these species to undergo hydrolysis to pH 8.3. Application of this definition shows that the computed acidity in mg L -1 as CaCO3 (based on pH and analytical concentrations of dissolved FeII, FeIII, Mn, and Al in mg L -1):aciditycalculated=50{1000(10-pH)+[2(FeII)+3(FeIII)]/56+2(Mn)/ 55+3(Al)/27}underestimates contributions from HSO4- and H+, but overestimates the acidity due to Fe3+ and Al3+. However, these errors tend to approximately cancel each other. It is demonstrated that "net alkalinity" is a valid mathematical construction based on theoretical definitions of alkalinity and acidity. Further, it is shown that, for most mine-drainage solutions, a useful net alkalinity value can be derived from: (1) alkalinity and acidity values based on aqueous speciation, (2) measured alkalinity minus calculated acidity, or (3) taking the negative of the value obtained in a

Comptonization in Ultra-Strong Magnetic Fields: Numerical Solution to the Radiative Transfer Problem

Science.gov (United States)

Ceccobello, C.; Farinelli, R.; Titarchuk, L.

2014-01-01

We consider the radiative transfer problem in a plane-parallel slab of thermal electrons in the presence of an ultra-strong magnetic field (B approximately greater than B(sub c) approx. = 4.4 x 10(exp 13) G). Under these conditions, the magnetic field behaves like a birefringent medium for the propagating photons, and the electromagnetic radiation is split into two polarization modes, ordinary and extraordinary, that have different cross-sections. When the optical depth of the slab is large, the ordinary-mode photons are strongly Comptonized and the photon field is dominated by an isotropic component. Aims. The radiative transfer problem in strong magnetic fields presents many mathematical issues and analytical or numerical solutions can be obtained only under some given approximations. We investigate this problem both from the analytical and numerical point of view, provide a test of the previous analytical estimates, and extend these results with numerical techniques. Methods. We consider here the case of low temperature black-body photons propagating in a sub-relativistic temperature plasma, which allows us to deal with a semi-Fokker-Planck approximation of the radiative transfer equation. The problem can then be treated with the variable separation method, and we use a numerical technique to find solutions to the eigenvalue problem in the case of a singular kernel of the space operator. The singularity of the space kernel is the result of the strong angular dependence of the electron cross-section in the presence of a strong magnetic field. Results. We provide the numerical solution obtained for eigenvalues and eigenfunctions of the space operator, and the emerging Comptonization spectrum of the ordinary-mode photons for any eigenvalue of the space equation and for energies significantly lesser than the cyclotron energy, which is on the order of MeV for the intensity of the magnetic field here considered. Conclusions. We derived the specific intensity of the

A plugging solution

Energy Technology Data Exchange (ETDEWEB)

Gen, O P; Azhigaliyev, G K; Dodonova, S Ye; Dyaltlova, N M; Novokhatskaya, I D; Ryabova, L I

1984-01-01

The purpose of the invention is to increase the durability of cement stone at 150 to 200C. The patent covers a plugging solution which consists of Portlandcement, sand and water. It additionally contains metal organic complexes of nitrylotrimethylphosphonic acid and organosiliconates of alkali or alkaline earth metals with the following component relationship in percent by mass: Portland cement, 42 to 43; sand, 27 to 28; metal organic complexes of nitrylotrimethylphosphonic acid, 0.01 to 1.5; organosiliconates of alkaline or alkaline earthmetals, 0.0025 to 0.375 and water, the remainder.

Influence of Experimental Parameters Using the Dip-Coating Method on the Barrier Performance of Hybrid Sol-Gel Coatings in Strong Alkaline Environments

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Rita B. Figueira

2015-04-01

Full Text Available Previous studies have shown that the barrier effect and the performance of organic-inorganic hybrid (OIH sol-gel coatings are highly dependent on the coating deposition method as well as on the processing conditions. However, studies on how the coating deposition method influences the barrier properties in alkaline environments are scarce. The aim of this experimental research was to study the influence of experimental parameters using the dip-coating method on the barrier performance of an OIH sol-gel coating in contact with simulated concrete pore solutions (SCPS. The influence of residence time (Rt, a curing step between each dip step and the number of layers of sol-gel OIH films deposited on hot-dip galvanized steel to prevent corrosion in highly alkaline environments was studied. The barrier performance of these OIH sol-gel coatings, named U(400, was assessed in the first instants of contact with SCPS, using electrochemical impedance spectroscopy and potentiodynamic methods. The durability and stability of the OIH coatings in SCPS was monitored during eight days by macrocell current density. The morphological characterization of the surface was performed by Scanning Electronic Microscopy before and after exposure to SCPS. Glow Discharge Optical Emission Spectroscopy was used to investigate the thickness of the U(400 sol-gel coatings as a function of the number of layers deposited with and without Rt in the coatings thickness.

Geochemical modeling of the influence of silicate mineral alteration on alkalinity production and carbonate precipitation

Science.gov (United States)

Herda, Gerhard; Kraemer, Stephan M.; Gier, Susanne; Meister, Patrick

2016-04-01

as well as carbonates in porefluids under different pCO2 levels. In a second step, we will let the minerals react to a thermodynamically stable state and thereby observe the resulting alkalinity effect and the effect on carbonate precipitation. So far, modeling showed that saturation states of some of the most common clay minerals, including kaolinite, illite, montmorillonite and chlorite in a standard seawater solution strongly depend on silica and aluminum concentrations, but they show very little dependence on the pH. This is understandable since a congruent dissolution of clay minerals does not significantly increase or decrease the alkalinity. However, partial leaching of structural ions by incongruent dissolution/precipitation should have a strong effect on porewater alkalinity. Hence, substitution reactions will have to be simulated as part of this study. Calculated mineral alteration and rock-fluid interactions in deep sediments will contribute to a better understanding of carbonate diagenesis but also of long-term effects in subsurface CO2 storage reservoirs. Mavromatis et al. (2014) Chem. Geol. 385, 84-91. Parkhurst, D.L, and Appelo, C.A.J. (2013) U.S Geological Survey Techniques and Methods, book 6, chap. A43, 497 p. Wallmann et al. (2008) Geochim. Cosmochim. Acta 72, 3067-3090.

On the capacity to the complexing of alkaline earth metal and magnesium chromates

International Nuclear Information System (INIS)

Orekhov, O.L.

1978-01-01

Considered is the capacity to the complexing of magnesium chromates and alkaline earth metal chromates with ammonium chromates in aqueous solutions. It has been established that the complexing of alkaline earth metal and magnesium chromates is effected by a nature of initial salts as well as their solubilities and the presence of crystallization water. Capacity of magnesium ions and alkaline rare earth metals to the complexing decreases in a series of Mg-Ca-Sr-Ba. Ca complexes exceed magnesium derivatives in respect of stability

Rb-Sr age of the Sivamalai alkaline complex, Tamil Nadu

International Nuclear Information System (INIS)

Subba Rao, T.V.; Narayana, B.L.; Gopalan, K.

1994-01-01

The Sivamalai alkaline complex comprises ferro-, pyroxene- hornblende-and nepheline-syenites. Field relations show that the nepheline syenites followed the emplacement of non-feldspathoidal syenites. Mineralogical data on the syenite suite have been reviewed. The Sivamalai alkaline rocks are not strongly enriched in rare-earth elements like most miaskites. Rb-Sr isotopic analyses of a suite of six samples from the various members of the complex define an isochron corresponding to an age of 623 ± 21 Ma (2σ) and initial Sr ratio of 0.70376 ± 14 (2σ). This is consistent with a model of fractional crystallization of a parent magma derived from an upper mantle source with apparently no isotopic evidence for more than one magma source for the complex. The Sivamalai alkaline complex represents a Pan-African alkaline magmatic event in the southern granulite terrane of peninsular India. (author). 26 refs., 4 figs., 4 tabs

Alkaline Activator Impact on the Geopolymer Binders

Science.gov (United States)

Błaszczyński, Tomasz Z.; Król, Maciej R.

2017-10-01

Concrete structures are constantly moving in the direction of improving the durability. Durability depends on many factors, which are the composition of concrete mix, the usage of additives and admixtures and the place, where material will work and carry the load. The introduction of new geopolymer binders for geopolymer structures adds a new aspect that is type of used activator. This substance with strongly alkaline reaction is divided because of the physical state, the alkaline degree and above all the chemical composition. Taking into account, that at present the geopolymer binders are made essentially from waste materials or by-products from the combustion of coal or iron ore smelting, unambiguous determination of the effect of the activator on the properties of the geopolymer material requires a number of trials, researches and observation. This paper shows the influence of the most alkaline activators on the basic parameters of the durability of geopolymer binders. In this study there were used highly alkaline hydroxides, water glasses and granules, which are waste materials in a variety of processes taking place in chemical plants. As the substrate of geopolymer binders there were used fly ash which came from coal and high calcareous ash from the burning of lignite.

Tungsten Recovery from Spent SCR Catalyst Using Alkaline Leaching and Ion Exchange

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Wen-Cheng Wu

2016-10-01

Full Text Available The recovery of tungsten (W from a honeycomb-type spent selective catalytic reduction (SCR catalyst using an alkaline leaching–ion exchange method was investigated. Spent SCR catalyst mainly consists of TiO2 and other oxides (6.37% W, 1.57% vanadium (V, and 2.81% silicon (Si, etc.. The ground catalyst was leached at the optimal conditions, as follows: NaOH concentration of 0.3 kg/kg of catalyst, pulp density of 3%, leaching temperature of 70 °C, particle size of −74 μm, and leaching time of 30 min. In this study, the leaching rate values of V and W under the above conditions were 87 wt %, and 91 wt %, respectively. The pregnant solution was then passed through a strong base anion exchange resin (Amberlite IRA900. At high pH conditions, the use of strong base anion exchange resin led to selective loading of divalent WO42− from the solution, because the fraction of two adjacent positively-charged sites on the IRA900 resin was higher and separate from the coexisting VO43−. The adsorbed W could then be eluted with 1 M NaCl + 0.5 M NaOH. The final concentrated W solution had 8.4 g/L of W with 98% purity. The application of this process in industry is expected to have an important impact on the recovery of W from secondary sources of these metals.

Strongly increasing solutions of cyclic systems of second order differential equations with power-type nonlinearities

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Jaroslav Jaroš

2015-01-01

Full Text Available We consider \\(n\\-dimensional cyclic systems of second order differential equations \\[(p_i(t|x_{i}'|^{\\alpha_i -1}x_{i}'' = q_{i}(t|x_{i+1}|^{\\beta_i-1}x_{i+1},\\] \\[\\quad i = 1,\\ldots,n, \\quad (x_{n+1} = x_1 \\tag{\\(\\ast\\}\\] under the assumption that the positive constants \\(\\alpha_i\\ and \\(\\beta_i\\ satisfy \\(\\alpha_1{\\ldots}\\alpha_n \\gt \\beta_1{\\ldots}\\beta_n\\ and \\(p_i(t\\ and \\(q_i(t\\ are regularly varying functions, and analyze positive strongly increasing solutions of system (\\(\\ast\\ in the framework of regular variation. We show that the situation for the existence of regularly varying solutions of positive indices for (\\(\\ast\\ can be characterized completely, and moreover that the asymptotic behavior of such solutions is governed by the unique formula describing their order of growth precisely. We give examples demonstrating that the main results for (\\(\\ast\\ can be applied to some classes of partial differential equations with radial symmetry to acquire accurate information about the existence and the asymptotic behavior of their radial positive strongly increasing solutions.

Effect of Alkaline Stress on Some Morphophysiologic Characteristics of Two Varieties of Safflower (Carthamus tinctorius L.

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Sh Bemany Golnabadi

2016-12-01

Full Text Available Introduction Safflower (Carthamus tinctorius L. is an important oilseed crop grown throughout the semiarid regions in many parts of the world. It has been cultivated for its oil and flowers and as a meal. Alkaline stress is caused by alkaline salts such as Na2CO3 or NaHCO3 in the soil. Alkaline stress, is widespread environmental constraint affecting crop productivity ,which can inhibit absorption of inorganic anions such as Cl–, NO3– and H2PO4–, greatly affect the selective absorption of K+-Na+, and break the ionic balance. However, under alkali stress, accumulation of compatible solutes, such as betaine, proline and soluble sugar into the vacuole are considered as the basic strategies for plant re-established cellular homeostasis. Some reports have clearly demonstrated that alkaline salts (NaHCO3 and Na2CO3 are more destructive to plants than neutral salts (NaCl and Na2SO4. Moreover, the salt-alkali stress can directly damage plant growth, alter the availability of nutrients and disrupt the balance of ions and mineral nutrition. The objective of this study was to investigate the effects of alkaline stress on growth and some physiological characteristics of safflower. Materials and Methods This study was conducted in a greenhouse in Vali-e-Asr University of Rafsanjan as factorial arrangement in completely randomized design with three replications. Experimental factors included alkaline stress in 7 levels (0, 10, 20, 30 , 40, 50 and 60 mM and two varieties of safflower (Sofeh and 411. Seeds were planted in pots filled with perlite and cocopite (1:1. The pots were irrigated with a nutrient solution with half strength Hoagland's solution. After the fourth true leaves appeared, alkaline stress in the pot was created by adding NaHCO3, to half strength Hoagland’s solution. Control plants were only irrigated with half strength Hoagland’s solution. Plants were harvested after 40 days of seed sowing. After forty days, shoot and root height

Leaching of the antimony and accompanying of elements Sb2S3 in the alkaline medium

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Dagmar Remeteiová

2007-06-01

Full Text Available This paper presents results of the laboratory investigation of alkaline leaching of stibnite that is an important mineral occuring in the antimony-bearing raw materials. The following components were present in stibnite: Sb2S3, SiO2, ZnS, FeS2. The aim of this study was to establish the effect of composition of the aqueous alkaline leaching medium (1 % NaOH, 1 % NaOH + 1 % Na2S2O3, 1 % NaOH + 1 % Na2S on the recoveries of Sb, Fe, Pb, Zn, Cu, Ni and Hg. The antimony recoveries in the leaching solutions NaOH and NaOH + Na2S2O3 solutions were lower in comparison with the leaching in NaOH + Na2S. The Fe, Pb, Zn recoveries in alkaline solutions were found to decrease in the following order: Fe, Pb, Zn. The mercury recovery in the leaching test with the solution containing 1 % NaOH+1 % Na2S was 3,7 %.

Exact Solution of a Strongly Coupled Gauge Theory in 0 +1 Dimensions

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Krishnan, Chethan; Kumar, K. V. Pavan

2018-05-01

Gauged tensor models are a class of strongly coupled quantum mechanical theories. We present the exact analytic solution of a specific example of such a theory: namely, the smallest colored tensor model due to Gurau and Witten that exhibits nonlinearities. We find explicit analytic expressions for the eigenvalues and eigenstates, and the former agree precisely with previous numerical results on (a subset of) eigenvalues of the ungauged theory. The physics of the spectrum, despite the smallness of N , exhibits rudimentary signatures of chaos. This Letter is a summary of our main results: the technical details will appear in companion paper [C. Krishnan and K. V. Pavan Kumar, Complete solution of a gauged tensor model, arXiv:1804.10103].

The Effect of Alkaline Activator Ratio on the Compressive Strength of Fly Ash-Based Geopolymer Paste

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Lăzărescu, A. V.; Szilagyi, H.; Baeră, C.; Ioani, A.

2017-06-01

Alkaline activation of fly ash is a particular procedure in which ash resulting from a power plant combined with a specific alkaline activator creates a solid material when dried at a certain temperature. In order to obtain desirable compressive strengths, the mix design of fly ash based geopolymer pastes should be explored comprehensively. To determine the preliminary compressive strength for fly ash based geopolymer paste using Romanian material source, various ratios of Na2SiO3 solution/ NaOH solution were produced, keeping the fly ash/alkaline activator ratio constant. All the mixes were then cured at 70 °C for 24 hours and tested at 2 and 7 days, respectively. The aim of this paper is to present the preliminary compressive strength results for producing fly ash based geopolymer paste using Romanian material sources, the effect of alkaline activators ratio on the compressive strength and studying the directions for future research.

Hydrophilic cobalt sulfide nanosheets as a bifunctional catalyst for oxygen and hydrogen evolution in electrolysis of alkaline aqueous solution.

Science.gov (United States)

Zhu, Mingchao; Zhang, Zhongyi; Zhang, Hu; Zhang, Hui; Zhang, Xiaodong; Zhang, Lixue; Wang, Shicai

2018-01-01

Hydrophilic medium and precursors were used to synthesize a hydrophilic electro-catalyst for overall water splitting. The cobalt sulfide (Co 3 S 4 ) catalyst exhibits a layered nanosheet structure with a hydrophilic surface, which can facilitate the diffusion of aqueous substrates into the electrode pores and towards the active sites. The Co 3 S 4 catalyst shows excellent bifunctional catalytic activity for both the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in alkaline solution. The assembled water electrolyzer based on Co 3 S 4 exhibits better performance and stability than that of Pt/C-RuO 2 catalyst. Thereforce the hydrophilic Co 3 S 4 is a highly promising bifunctional catalyst for the overall water splitting reaction. Copyright © 2017 Elsevier Inc. All rights reserved.

Selective leaching of Zn from spent alkaline batteries using environmentally friendly approaches.

Science.gov (United States)

Maryam Sadeghi, S; Vanpeteghem, Guillaumme; Neto, Isabel F F; Soares, Helena M V M

2017-02-01

The main aim of this work was to evaluate the possibility of using microwave or ultrasound to assist the efficient and selective leaching of Zn from spent alkaline batteries and compare the results with those obtained using the conventional method. Two different strategies were applied: acid leaching of a washed residue and alkaline leaching of the original residue. In both (acid and alkaline) approaches, the use of microwave- or ultrasound-assisted leaching increased the extraction of Zn compared with the best results obtained using conventional leaching [acid leaching (1.5mol/L H 2 SO 4 , 3h, 80°C), 90% of Zn extracted; alkaline leaching (6mol/L NaOH, 3h, 80°C), 42% of Zn extracted]. With acid leaching, 94% of the Zn was extracted using microwave-assisted leaching (1 cycle, 30s, 1mol/L H 2 SO 4 ), and 92% of the Zn was extracted using ultrasound-assisted leaching (2min, 0.1p, 20% amplitude, 1mol/L H 2 SO 4 ). Ultrasound-assisted leaching resulted in a more selective (Zn/Mn ratio of 5.1) Zn extraction than microwave-assisted leaching (Zn/Mn ratio of 3.5); both processes generated a concentrated Zn solution (⩾18.7g/L) with a purity (83.3% and 77.7%, respectively) that was suitable for electrowinning. With alkaline leaching, microwave- (1 cycle, 3 min, 4mol/L NaOH) and ultrasound-assisted (14min, 0.1p, 20% amplitude, 4mol/L NaOH) leaching extracted about 80% of the Zn and less than 0.01% of the Mn, which resulted in lesser concentrated Zn solutions (approximately 16.5g/L) but with high purity (>99.5%) that was suitable for the recovery of Zn by precipitation. The microwave- and ultrasound-assisted leaching strategies used in this work proved to be efficient and environmentally-friendly approaches for the extraction of Zn from spent alkaline residues since a concentrated Zn solution with adequate purity for subsequent Zn recovery was obtained using significantly decreased leaching times and concentrations of chemicals. Copyright © 2017 Elsevier Ltd. All rights

Evaluation of hydraulic conductivities of bentonite and rock under hyper alkaline and nitrate conditions (3)

International Nuclear Information System (INIS)

Iriya, Keishiro; Kubo, Hiroshi

2004-02-01

Circumstance of TRU waste repository shows alkaline condition due to leaching of cementitious materials. The waste containing significant soluble nitrate may changes ground water chemistry to high ion strength. Consolidation test and permeability test are carried out in order to assess quantitatively permeability of bentonite altered by hyper alkaline and nitrate. Modeling is progressed based on experimental results. The following results are obtained. 1) Consolidation test was carried out in 3 types of bentonite and 30 % sand mixture in which cation exchanged with nitrate. It is noted that permeability of bentonite increased at from 40 to 200 times by cation exchange. 2) Permeability of hyper alkaline solution is almost same to water. Permeability of hyper alkaline solution with nitrates increased corresponding to rising ion strength. 3) The results of batch of column test were simulated. The model can explain clearly the results in short period. This can estimate leaching ratio and secondary minerals. The model can simulate the experimental results by two types of velocity theory on altering bentonite. (author)

Study of the electroreduction of nitrate on copper in alkaline solution

Energy Technology Data Exchange (ETDEWEB)

Reyter, David [INRS Energie, Materiaux et Telecommunications, 1650 bd. Lionel Boulet, Varennes, Qc (Canada); Departement de Chimie, Universite du Quebec a Montreal, CP 8888, Montreal, Qc (Canada); Belanger, Daniel [Departement de Chimie, Universite du Quebec a Montreal, CP 8888, Montreal, Qc (Canada); Roue, Lionel [INRS Energie, Materiaux et Telecommunications, 1650 bd. Lionel Boulet, Varennes, Qc (Canada)

2008-08-20

The electrocatalytic activity of a Cu electrode for the electroreduction of nitrate in alkaline medium was investigated by linear sweep voltammetry at stationary and rotating disc electrodes. Nitrate-reduction products generated upon prolonged electrolyses at different potentials were quantified. In addition, adsorption phenomena associated with the nitrate electroreduction process were characterized by electrochemical quartz crystal microbalance (EQCM) experiments. This data revealed that nitrate electroreduction process strongly depends on the applied potential. Firstly, at ca. -0.9 V vs. Hg/HgO, the electroreduction of adsorbed nitrate anions to nitrite anions was identified as the rate-determining step of the nitrate electroreduction process. Between -0.9 and -1.1 V, nitrite is reduced to hydroxylamine. However, during long-term electrolyses, hydroxylamine is not detected and presumably because it is rapidly reduced to ammonia. At potential more negative than -1.1 V, nitrite is reduced to ammonia. At ca. -1.45 V, i.e. just before the hydrogen evolution reaction, the abrupt decrease of the cathodic current is due to the electrode poisoning by adsorbed hydrogen. In addition, during the first minutes of nitrate electrolysis, a decrease of the copper electrode activity was observed at the three investigated potentials (-0.9, -1.1 and -1.4 V). From polarization and EQCM measurements, this deactivation was attributed to the adsorption of nitrate-reduction products, blocking the electrode surface and slowing down the nitrate electroreduction rate. However, it was demonstrated that the Cu electrode can be reactivated by the periodic application of a square wave potential pulse at -0.5 V, which causes the desorption of poisoning species. (author)

Process optimization and leaching kinetics of zinc and manganese metals from zinc-carbon and alkaline spent batteries using citric acid reagent

Science.gov (United States)

Yuliusman; Amiliana, R. A.; Wulandari, P. T.; Huda, M.; Kusumadewi, F. A.

2018-03-01

Zn-Carbon and Alkaline spent batteries contains heavy metals, such as zinc and manganese, which can causes environmental problem if not handled properly. Usually the recovery of these metals were done by leaching method using strong acid, but the use of strong acids as leaching reagents can be harmful to the environment. This paper concerns the recovery of Zn and Mn metals from Zn-C and alkaline spent batteries with leaching method using citric acid as the environmental friendly leaching reagent. The leaching conditions using citric acid were optimized and the leaching kinetics of Zn and Mn in citric acid solution was investigated. The leaching of 89.62% Zn and 63.26% Mn was achieved with 1.5 M citric acid, 90°C temperature, and 90 minutes stirring time. Kinetics data for the dissolution of Zn showed the best fit to chemical control shrinking core model, while the diffusion controlled model was suitable for the dissolution of Mn kinetics data. The activation energy of 6.12 and 1.73 kcal/mol was acquired for the leaching of Zn and Mn in the temperature range 60°C-90°C.

Comparison of anti-corrosive properties between hot alkaline nitrate blackening and hydrothermal blackening routes

Energy Technology Data Exchange (ETDEWEB)

Fattah-alhosseini, A. [Department of Materials Engineering, Bu-Ali Sina University, Hamedan 65178-38695 (Iran, Islamic Republic of); Yazdani Khan, H., E-mail: hamid.yazdanikhan@gmail.com [Department of Materials Engineering, Bu-Ali Sina University, Hamedan 65178-38695 (Iran, Islamic Republic of); Heidarpour, A. [Department of Metallurgy and Materials Engineering, Hamedan University of Technology, Hamedan, 65155-579 (Iran, Islamic Republic of)

2016-08-15

In this study, the oxide films were formed on carbon steel by using hot alkaline nitrate and hydrothermal treatments. A dense and protective oxide film was obtained by hydrothermal method due to application of high pressure and by increasing solution temperature from boiling temperature (155 °C) to 250 °C. Oxide films were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), and electrochemical tests including potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). These analyses showed that the magnetite film which was formed on carbon steel surface by hydrothermal treatment offers the best resistance in 3.5 wt.% NaCl solution. Although thicker oxide film could be obtained via hot alkaline nitrate black oxidizing, corrosion resistance was lower as a result of being highly porous and the presence of hematite. - Highlights: • Oxide films have been formed on steel by using of hot alkaline nitrate and hydrothermal treatments. • A dense and protective oxide film was obtained by hydrothermal treatment. • SEM micrographs showed that a dense and protective oxide film was obtained by hydrothermal treatment. • Film formed by hydrothermal treatment could have the best resistance in 3.5 wt.% NaCl solution.

State of the Art on Cactus Additions in Alkaline Media as Corrosion Inhibitors

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A. A. Torres-Acosta

2012-01-01

Full Text Available This research in progress includes results on the corrosion performance of reinforcing steel in alkaline media when two different dehydrated cacti (Opuntia ficus-indica—Nopal—and Aloe Vera were used as additions in pH 12.5 and 13.3 solutions and in concrete. The dehydrated cactus addition was mixed at different concentrations by either solution or cement mass (0.10%, 0.25%, 0.5%, 1.0%, and 2.0%. Half-cell potentials and LPR measurements were performed at different time periods to characterize the possible corrosion inhibiting effect of the cactus additions tested in such alkaline media. Results showed good corrosion inhibiting effect of dehydrated Nopal on reinforcing steel, in all tested solutions, when chloride ions are present. Aloe Vera did show also corrosion inhibiting improvements in some extent. The addition of such cactus led to an apparent formation of a denser and more packed oxide/hydroxide surface layer on the steel surface that decreased corrosion activity. This oxide/hydroxide layer growth was confirmed by microscopic evaluation of the metal surface layer performed at the end of the research program. The preliminary findings suggest that adding Nopal at concentrations between 1% and 2%, by mass, might be suitable for durability enhancing applications in alkaline media, especially in concrete structures.

Application conditions for ester cured alkaline phenolic resin sand

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Ren-he Huang

2016-07-01

Full Text Available Five organic esters with different curing speeds: propylene carbonate (i.e. high-speed ester A; 1, 4-butyrolactone; glycerol triacetate (i.e. medium-speed ester B; glycerol diacetate; dibasic ester (DBE (i.e. low-speed ester C, were chosen to react with alkaline phenolic resin to analyze the application conditions of ester cured alkaline phenolic resin. The relationships between the curing performances of the resin (including pH value, gel pH value, gel time of resin solution, heat release rate of the curing reaction and tensile strength of the resin sand and the amount of added organic ester and curing temperature were investigated. The results indicated the following: (1 The optimal added amount of organic ester should be 25wt.%-30wt.% of alkaline phenolic resin and it must be above 20wt.%-50 wt.% of the organic ester hydrolysis amount. (2 High-speed ester A (propylene carbonate has a higher curing speed than 1, 4-butyrolactone, and they were both used as high-speed esters. Glycerol diacetate is not a high-speed ester in alkaline phenolic resin although it was used as a high-speed ester in ester cured sodium silicate sand; glycerol diacetate and glycerol triacetate can be used as medium-speed esters in alkaline phenolic resin. (3 High-speed ester A, medium-speed ester B (glycerol triacetate and low-speed ester C (dibasic ester, i.e., DBE should be used below 15 ìC, 35 ìC and 50 ìC, respectively. High-speed ester A or low-speed ester C should not be used alone but mixed with medium-speed ester B to improve the strength of the resin sand. (4 There should be a suitable solid content (generally 45wt.%-65wt.% of resin, alkali content (generally 10wt.%-15wt.% of resin and viscosity of alkaline phenolic resin (generally 50-300 mPa≤s in the preparation of alkaline phenolic resin. Finally, the technique conditions of alkaline phenolic resin preparation and the application principles of organic ester were discussed.

The Effect of Alkaline Concentration on Coconut Husk Crystallinity and the Yield of Sugars Released

Science.gov (United States)

Sangian, H. F.; Widjaja, A.

2018-02-01

This work was to analyze the effect of alkaline concentration on coconut coir husk crystallinity and sugar liberated enzymatically. The data showed that the employing of alkaline on lignocellulose transformed the crystallinity. The XRD peaks increased highly which indicated that cellulose was more opened and exposed. After pretreatment, the chemical compositions (cellulose, hemicellulose, and lignin) were changed significantly. The employing 1% alkaline, the cellulosic content inclined if compared to that of non-pretreatment. When the alkaline concentration was added to 4%, the cellulose was decreased slightly which indicated that a part of cellulose and hemicellulose was dissolved into solution. It was found the alkaline pretreatment influenced by the biochemical reaction of treated substrates in producing the reducing sugars. The amounts of sugar liberated enzymatically of coconut husk treated by 1% and 4% alkaline increased to 0.26, and 0.24 g sugar/g (cellulose+hemicellulose), respectively, compared to that of native solid recorded at 0.18 g sugar/g (cellulose+hemicellulose).

Distributions of 14 elements on 60 selected absorbers from two simulant solutions (acid-dissolved sludge and alkaline supernate) for Hanford HLW Tank 102-SY

International Nuclear Information System (INIS)

Marsh, S.F.; Svitra, Z.V.; Bowen, S.M.

1993-10-01

Sixty commercially available or experimental absorber materials were evaluated for partitioning high-level radioactive waste. These absorbers included cation and anion exchange resins, inorganic exchangers, composite absorbers, and a series of liquid extractants sorbed on porous support-beads. The distributions of 14 elements onto each absorber were measured from simulated solutions that represent acid-dissolved sludge and alkaline supernate solutions from Hanford high-level waste (HLW) Tank 102-SY. The selected elements, which represent fission products (Ce, Cs, Sr, Tc, and Y); actinides (U, Pu, and Am); and matrix elements (Cr, Co, Fe, Mn, Zn, and Zr), were traced by radionuclides and assayed by gamma spectrometry. Distribution coefficients for each of the 1680 element/absorber/solution combinations were measured for dynamic contact periods of 30 min, 2 h, and 6 h to provide sorption kinetics information for the specified elements from these complex media. More than 5000 measured distribution coefficients are tabulated

Evaluation of hydraulic conductivities of bentonite and rock under hyper alkaline and nitrate conditions (3) (Summary)

International Nuclear Information System (INIS)

Iriya, Keishiro; Kubo, Hiroshi

2004-02-01

This report is the summary of JNC-TJ--8400-2005-002. 1) Circumstance of TRU waste repository shows alkaline condition due to leaching of cementitious materials. The waste containing significant soluble nitrate may changes ground water chemistry to high ion strength. Consolidation test and permeability test are carried out in order to as. exchanged with nitrate. It is noted that permeability of bentonite increased at from 40 to 200 times by cation exchange. 2) Permeability of hyper alkaline solution is almost same to water. Permeability of hyper alkaline solution with nitrates increased corresponding to rising ion strength. 3) The results of batch of column test were simulated. The model can explain clearly the results in short period. This can estimate leaching ratio and secondary minerals. The model can simulate the experimental results by two types of velocity theory on altering bentonite. (author)

Catalytic Activity of Urchin-like Ni nanoparticles Prepared by Solvothermal Method for Hydrogen Evolution Reaction in Alkaline Solution

International Nuclear Information System (INIS)

Abbas, Syed Asad; Iqbal, Muhammad Ibrahim; Kim, Seong-Hoon; Jung, Kwang-Deog

2017-01-01

Highlights: • Urchin-like Ni is prepared in solvothermal reaction. • Urchin-like Ni is formed via Ni(OH) 2 aggregates in ethanol and oleylamine. • Exchange current density of urchin-like Ni is 0.191 mA cm −2 . • Urchin-like Ni exceeds the catalytic performance of commercial Pt/C in HER. - Abstract: Ni nanoparticles with different morphologies were synthesized for hydrogen evolution reaction (HER) in alkaline solution. Here, Ni(acac) 2 was converted into Ni metal nanoparticles in solvothermal reactions with simple alcohols and oleylamine (OAm). The morphology of the resulting Ni nanoparticles was dependent mainly on the OAm/Ni molar ratio in alcohol solvent. Aggregates of spherical Ni nanoparticles (NiEt-OAm1) were observed at the OAm/Ni molar ratio of 1.0, whereas two echinoid Ni nanoparticles (NiEt-OAm4 and NiEt-OAm6) could be prepared in ethanol at the OAm/Ni molar ratios of 4.0 and 6.0. Ni(OH) 2 formed in ethanol during a reaction time of 5 h was then reduced into echinoid Ni nanoparticles after 8 h. Echinoid Ni nanoparticles were formed by atomic addition on the tops of the multipod Ni particles formed via Ni(OH) 2 /NiO aggregates. Webbed feet-like particles (NiIPA-OAm4) with plate edges were also observed in isopropanol under the same reaction conditions. The catalytic activities of the prepared Ni nanoparticles for the hydrogen evolution reaction were evaluated in alkaline solution. The NiEt-OAm4 with urchin-like morphology was much more active than the NiIPA-OAm4 with webbed feet-like morphology. The exchange current density of Ni catalysts was increased with increasing the OAm/Ni molar ratio. The NiEt-OAm6 exhibited an exchange current of 0.191 mA cm −2 and the NiEt-OAm4 exceeded electrocatalytic performance of a commercial Pt catalysts (40% Pt on Vulcan XC 72) in a stability test for 100 kiloseconds at −1.5 V (vs. Hg/HgO) in 1.0 M NaOH due to its high stability.

Coprecipitation of 137Cs and 85Sr microquantities with complex compound [M(18-crown-6)]BPH4 (M=Na+, Cs+) from neutral and alkaline solutions

International Nuclear Information System (INIS)

Konovalova, N.A.; Rumer, I.A.; Kulyukhin, S.A.

2009-01-01

The paper reports the possibility of joint separation of 137 Cs and 85 Sr from neutral and alkaline aqueous solutions by their coprecipitation with the solid phase of complex compounds [M(18-crown-6)]BPh 4 (M=Na + , Cs + ), as well as to study the coprecipitation of 137 Cs and 85 Sr with the solid phase CsBPh 4 . It is found that complex compounds [M(18-crown-6)]BPh 4 (M=Na + , Cs + ) increased the degree of 85 Sr separation from solutions virtually two- to threefold vs. CsBPh 4 . Chloride and nitrate were found to have hardly any impact on the coprecipitation of 137 Cs and 85 Sr with [M(18-crown-6)]BPh 4 (M = Na + , Cs + ). (orig.)

Development of Al2O3 carrier-Ru composite catalyst for hydrogen generation from alkaline NaBH4 hydrolysis

International Nuclear Information System (INIS)

Huang, Yao-Hui; Su, Chia-Chi; Wang, Shu-Ling; Lu, Ming-Chun

2012-01-01

A recyclable and reusable Ru/Al 2 O 3 catalyst is prepared for hydrogen generation from the hydrolysis process of alkaline sodium borohydride (NaBH 4 ) solution. The hydrogen generation rate by the hydrolysis and methanolysis of alkaline NaBH 4 was explored as a function of NaOH concentration. Meantime, the byproducts derived from the spent alkaline NaBH 4 solution were characterized by X-ray diffraction (XRD), scanning electro microscope/energy dispersive spectrometer (SEM/EDS) and NMR (Nuclear Magnetic Resonance). The effect of NaOH concentration on the hydrogen generation from the hydrolysis of NaBH 4 significantly depends on the type of catalysts. With increasing NaOH concentration, the hydrogen generation rates decrease when using ruthenium (Ru) composite as a catalyst. The hydrogen generation rate of the methanolysis of NaBH 4 is significantly inhibited in the presence of NaOH as compared with the hydrolysis of NaBH 4 . The durability test of the Ru/Al 2 O 3 catalyst shows that the hydrogen generation rate decreases with recycling and reuse. The XRD and NMR analysis results show that the borate hydrate (NaBO 2 H 2 O) was derived from the hydrolysis of 20 wt% and 30 wt% NaBH 4 . -- Highlights: ► A recyclable Ru/Al 2 O 3 catalyst was synthesized for hydrogen generation. ► Ru/Al 2 O 3 significantly promotes the hydrogen generation rate from alkaline NaBH 4 solution. ► The prepared Ru/Al 2 O 3 catalyst can easily collect from the spent alkaline NaBH 4 solution.

Chemical nickel plating in tartrate solutions with borohydride reducing agent

International Nuclear Information System (INIS)

Plokhov, V.A.

1986-01-01

The authors investigate the influence of various factors on the rate of chemical nickel plating in strongly alkaline tartrate solutions with a borohydride reducing agent. After 30 min of the process of nickel plating, the final concentration of sodium borohydride decreases to 0.26 g/liter, leading to stoppage of the process. The nickel plating process can be intensified by increasing the concentration of sodium hydroxide in the solution, suppressing hydrolysis of borohydride, and also by introducing additives which suppress hydrolysis of borohydride. For chemical deposition of nickel-boron coatings from tartrate solutions the authors recommend the following composition (g/liter): nickel chloride 15-25, Rochelle salt 450-550, sodium hydroxide 140-160, sodium borohydride 0.8-1.0, thallium nitrate 0.003-0.008. The process temperature is 92-95 C, and the deposition rate is 4-6 um/h

Aluminum anode for aluminum-air battery - Part II: Influence of In addition on the electrochemical characteristics of Al-Zn alloy in alkaline solution

Science.gov (United States)

Park, In-Jun; Choi, Seok-Ryul; Kim, Jung-Gu

2017-07-01

Effects of Zn and In additions on the aluminum anode for Al-air battery in alkaline solution are examined by the self-corrosion rate, cell voltage, current-voltage characteristics, anodic polarization, discharge performance and AC impedance measurements. The passivation behavior of Zn-added anode during anodic polarization decreases the discharge performance of Al-air battery. The addition of In to Al-Zn anode reduces the formation of Zn passivation film by repeated adsorption and desorption behavior of In ion onto anode surface. The attenuated Zn passive layer by In ion attack leads to the improvement of discharge performance of Al-air battery.

The viability of MCM-41 as separator in secondary alkaline cells

Science.gov (United States)

Meskon, S. R.; Othman, R.; Ani, M. H.

2018-01-01

The viability of MCM-41 membrane as a separator material in secondary alkaline cell is investigated. The inorganic membrane was employed in an alkaline nickel-zinc system. MCM-41 mesoporous material consists of arrays of hexagonal nano-pore channels. The membrane was synthesized using sol-gel route from parent solution comprising of quarternary ammonium surfactant, cethyltrimethylammonium bromide C16H33(CH3)3NBr (CTAB), hydrochloric acid (HCl), deionized water (H2O), ethanol (C2H5OH), and tetraethylortosilicate (TEOS). Both the anodic zinc/zinc oxide and cathodic nickel hydroxide electrodeposited film were coated with MCM-41 membrane. The Ni/MCM-41/Zn alkaline cell was then subjected to 100-cycle durability test and the structural stability of MCM-41 separator throughout the progression of the charge-discharge cycles is studied. X-ray diffraction (XRD) analysis on the dismantled cell shows that MCM-41 began to transform to lamellar MCM-50 on the 5th cycle and transformed almost completely on the 25th cycle. The phase transformation of MCM-41 hexagonal structure into gel-like MCM-50 prevents the mesoporous cell separator from diminished in the caustic alkaline surround. This work has hence demonstrated MCM-41 membrane is viable to be employed in secondary alkaline cells.

Strong solutions for an incompressible Navier-Stokes/Allen-Cahn system with different densities

Science.gov (United States)

Li, Yinghua; Huang, Mingxia

2018-06-01

In this paper, we investigate a coupled Navier-Stokes/Allen-Cahn system describing a diffuse interface model for two-phase flow of viscous incompressible fluids with different densities in a bounded domain Ω \\subset R^N(N=2,3). We prove the existence and uniqueness of local strong solutions to the initial boundary value problem when the initial density function ρ _0 has a positive lower bound.

Non-polluting treatment of uranium effluents from the alkaline digestion of an uranium ore containing sulfur

International Nuclear Information System (INIS)

Berger, Bernard.

1978-01-01

New non-polluting process for treating uranium effluents from the alkaline digestion of an uranium ore containing sulphur, which makes it possible (a) to extract and obtain relatively pure uranium and (b) to process the digestion liquor freed from the uranium and containing in an aqueous solution a mixture of alkaline carbonate and/or bicarbonate and sodium sulphate, consisting in the selective extraction of the sodium sulphate present and the recycling of the liquor free of SO 4 = ions, containing in solution the sole carbonates and/or bicarbonates involved, towards the digestion of the ore [fr

Reduction of nitrobenzene with alkaline ascorbic acid: Kinetics and pathways

International Nuclear Information System (INIS)

Liang, Chenju; Lin, Ya-Ting; Shiu, Jia-Wei

2016-01-01

Highlights: • Alkaline ascorbic acid (a.k.a. vitamin C) is capable of reductively degrading NB. • The pH above the pK_a_2 of ascorbic acid increases reductive electron transfer to NB. • The rate equation for the reactions between NB and AA is determined. • NSB, AZOXY, and AZO are identified as intermediates and aniline as a final product. • Alkaline pH is essential for AA remediation of NB contaminated soils. - Abstract: Alkaline ascorbic acid (AA) exhibits the potential to reductively degrade nitrobenzene (NB), which is the simplest of the nitroaromatic compounds. The nitro group (NO_2"−) of NB has a +III oxidation state of the N atom and tends to gain electrons. The effect of alkaline pH ranging from 9 to 13 was initially assessed and the results demonstrated that the solution pH, when approaching or above the pK_a_2 of AA (11.79), would increase reductive electron transfer to NB. The rate equation for the reactions between NB and AA at pH 12 can be described as r = ((0.89 ± 0.11) × 10"−"4 mM"1"−"("a "+ "b") h"−"1) × [NB]"a "= "1"."3"5 "± "0"."1"0[AA]"b "= "0"."8"9 "± "0"."0"1. The GC/MS analytical method identified nitrosobenzene, azoxybenzene, and azobenzene as NB reduction intermediates, and aniline (AN) as a final product. These experimental results indicate that the alkaline AA reduction of NB to AN mainly proceeds via the direct route, consisting of a series of two-electron or four-electron transfers, and the condensation reaction plays a minor route. Preliminary evaluation of the remediation of spiked NB contaminated soils revealed that maintenance of alkaline pH and a higher water to soil ratio are essential for a successful alkaline AA application.

Lignocellulosic Composites Prepared Utilizing Aqueous Alkaline/Urea Solutions with Cold Temperatures

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Brent Tisserat

2018-01-01

Full Text Available Lignocellulosic composites (LCs were fabricated by partially dissolving cotton to create a matrix that was reinforced with osage orange wood (OOW particles and/or blue agave fibers (AF. LCs were composed of 15–35% cotton matrix and 65–85% OWW/AF reinforcement. The matrix was produced by soaking cotton wool in a cold aqueous alkaline/urea solvent and was stirred for 15 minutes at 350 rpm to create a viscous gel. The gel was then reinforced with lignocellulosic components, mixed, and then pressed into a panel mold. LC panels were soaked in water to remove the aqueous solvent and then oven dried to obtain the final LC product. Several factors involved in the preparation of these LCs were examined including reaction temperatures (−5 to −15°C, matrix concentration (15–35% cotton, aqueous solvent volume (45–105 ml/panel, and the effectiveness of employing various aqueous solvent formulations. The mechanical properties of LCs were determined and reported. Conversion of the cotton into a suitable viscous gel was critical in order to obtain LCs that exhibited high mechanical properties. LCs with the highest mechanical properties were obtained when the cotton wools were subjected to a 4.6% LiOH/15% urea solvent at −12.5°C using an aqueous solvent volume of 60 ml/panel. Cotton wool subjected to excessive cold alkaline solvents volumes resulted in irreversible cellulose breakdown and a resultant LC that exhibited poor mechanical properties.

Alkaline leaching for synthesis of improved Fe-ZSM5 catalysts

NARCIS (Netherlands)

Espinosa, S; Mentruit, C; Kapteijn, F; Moulijn, JA; Melián-Cabrera, I.

Fe-ZSM5 catalysts were fully Fe-exchanged by pretreating the parent zeolite with base a solution prior to the Fe-exchange. The catalysts prepared in this way showed very low amount of inactive FeOx and improved performance in N2O decomposition. Alkaline leaching breaks down the zeolite crystals -

Alkalinity in oil field waters - what alkalinity is and how it is measured

International Nuclear Information System (INIS)

Kaasa, B.; Oestvold, T.

1996-01-01

The alkalinity is an important parameter in the description of pH-behaviour, buffer capacity and scaling potentials in oil field waters. Although the alkalinity is widely used, it seems to be considerable confusion in connection with the concept. It is often used incorrectly and different authors define the concept in different ways. Several different methods for the determination of alkalinity can be found in the literature. This paper discusses the definition of alkalinity and how to use alkalinity in oil field waters to obtain data of importance for scale and pH predictions. There is also shown how a simple titration of oil field waters can give both the alkalinity and the content of organic acids in these waters. It is obvious from these findings that most of the methods used to day may give considerable errors when applied to oil field waters with high contents of organic acids. 8 refs., 8 figs., 5 tabs

Alkalinity production in intertidal sands intensified by lugworm bioirrigation.

Science.gov (United States)

Rao, Alexandra M F; Malkin, Sairah Y; Montserrat, Francesc; Meysman, Filip J R

2014-07-05

Porewater profiles and sediment-water fluxes of oxygen, nutrients, pH, calcium, alkalinity, and sulfide were measured in intertidal sandflat sediments from the Oosterschelde mesotidal lagoon (The Netherlands). The influence of bioturbation and bioirrigation by the deep-burrowing polychaete Arenicola marina on the rates and sources of benthic alkalinity generation was examined by comparing measurements in intact and defaunated sediment cores before and after the addition of A. marina in summer and fall 2011. Higher organic matter remineralization rates, shallower O 2 penetration, and greater sediment-water solute fluxes were observed in summer, consistent with higher sediment community metabolic rates at a higher temperature. Lugworm activity stimulated porewater exchange (5.1 × in summer, 1.9 × in fall), organic matter remineralization (6.2 × in summer, 1.9 × in fall), aerobic respiration (2.4 × in summer, 2.1 × in fall), alkalinity release (4.7 × in summer, 4.0 × in fall), nutrient regeneration, and iron cycling. The effects of lugworm activity on net sediment-water fluxes were similar but more pronounced in summer than in fall. Alkalinity release in fall was entirely driven by metabolic carbonate dissolution, while this process explained between 22 and 69% of total alkalinity production in summer, indicating the importance of other processes in this season. By enhancing organic matter remineralization and the reoxidation of reduced metabolites by the sediment microbial community, lugworm activity stimulated the production of dissolved inorganic carbon and metabolic acidity, which in turn enhanced metabolic CaCO 3 dissolution efficiency. In summer, evidence of microbial long distance electron transport (LDET) was observed in defaunated sediment. Thus, alkalinity production by net carbonate dissolution was likely supplemented by anaerobic respiration and LDET in summer.

Effective Uranium (VI) Sorption from Alkaline Solutions Using Bi-Functionalized Silica-Coated Magnetic Nanoparticles

International Nuclear Information System (INIS)

Chen, X.; He, L.; Liu, B.; Tang, Y.

2015-01-01

High temperature gas reactor is one of generation IV reactors that can adapt the future energy market, of which the preparation of fuel elements will produce a large amount of radioactive wastewater with uranium and high-level ammonia. Sorption treatment is one of the most important method to recover uranium from wastewater. However, there are few report on uranium sorbent that can directly be applied in wastewater with ammonia. Therefore, the development of a sorbent that can recover uranium in basic environment will greatly decrease the cost of fuel element production and the risk of radioactive pollution. In this work, ammonium-phosphonate-bifunctionalized silica-coated magnetic nanoparticles has been developed for effective sorption of uranium from alkaline media, which are not only advantaged in the uranium separation from liquid phase, but also with satisfactory adsorption rate, amount and reusability. The as-prepared sorbent is found to show a maximum uranium sorption capacity of 70.7 mg/g and a fast equilibrium time of 2 h at pH 9.5 under room temperature. Compared with the mono-functionalized (phosphonate alone and ammonium alone) particles, the combination of the bi-functionalized groups gives rise to an excellent ability to remove uranium from basic environment. The sorbent can be used as a promising solid phase candidate for highly-efficient removal of uranium from basic solution. (author)

Comparative Study of the Preparation of Reducing Sugars Hydrolyzed from High-Lignin Lignocellulose Pretreated with Ionic Liquid, Alkaline Solution and Their Combination

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Hanny F. Sangian

2015-05-01

Full Text Available The ionicliquid [MMIM][DMP] was synthesized from the reactants methyl imidazole [MIM] and trimethylphosphate [TMP] and verified using 1HNMR and FTIR. Coconut coir dust was pretreated with a 1% alkaline solution.Its crystalline structure increased significantly due to the dissolution of lignin and hemicelluloses under alkaline conditions, exposing the cellulose. After NaOH and IL were employed, the XRD showed that peak (002 decreased significantly and peak (101 almost vanished. This significant decrease in crystallinity was related to the alteration of the substrate from the cellulose I structure to the cellulose II structure. The pretreated substrates were hydrolyzed to convert them to reducing sugars by pure cellulase and xylanase,and the reaction was conducted at 60°C, pH 3, for 12 or 48 hours. The yields of sugar hydrolyzed from untreated and NaOH-pretreated substrates were 0.07 and 0.12 g sugar/g lignocellulose, respectively. Pretreatment with IL or the combination of NaOH+IL resulted in yields of reducing sugars of 0.11 and 0.13 g/g, respectively. These findings showed that IL pretreatment of the high-lignin lignocellulose is a new prospect for the economical manufacture of reducing sugars and bioethanol in the coming years.

Effect of Sn4+ Additives on the Microstructure and Corrosion Resistance of Anodic Coating Formed on AZ31 Magnesium Alloy in Alkaline Solution

Science.gov (United States)

Salman, S. A.; Kuroda, K.; Saito, N.; Okido, M.

Magnesium is the lightest structural metal with high specific strength and good mechanical properties. However, poor corrosion resistance limits its widespread use in many applications. Magnesium is usually treated with Chromate conversion coatings. However, due to changing environmental regulations and pollution prevention requirements, a significant push exists to find new, alternative for poisonous Cr6+. Therefore, we aim to improve corrosion resistance of anodic coatings on AZ31 alloys using low cost non-chromate electrolyte. Anodizing was carried out in alkaline solutions with tin additives. The effect of tin additives on the coating film was characterized by SEM and XRD. The corrosion resistance was evaluated using anodic and cathodic polarizations and electrochemical impedance spectroscopy (EIS). Corrosion resistance property was improved with tin additives and the best anti-corrosion property was obtained with addition of 0.03 M Na2SnO3.3H2O to anodizing solution.

Mechanistic insights into the bleaching of melanin by alkaline hydrogen peroxide.

Science.gov (United States)

Smith, R A W; Garrett, B; Naqvi, K R; Fülöp, A; Godfrey, S P; Marsh, J M; Chechik, V

2017-07-01

This work aims to determine the roles of reactive oxygen species HO∙ and HO 2 - in the bleaching of melanins by alkaline hydrogen peroxide. Experiments using melanosomes isolated from human hair indicated that the HO∙ radical generated in the outside solution does not contribute significantly to bleaching. However, studies using soluble Sepia melanin demonstrated that both HO 2 - and HO∙ will individually bleach melanin. Additionally, when both oxidants are present, bleaching is increased dramatically in both rate and extent. Careful experimental design enabled the separation of the roles and effects of these key reactive species, HO∙ and HO 2 - . Rationalisation of the results presented, and review of previous literature, allowed the postulation of a simplified general scheme whereby the strong oxidant HO∙ is able to pre-oxidise melanin units to o-quinones enabling more facile ring opening by the more nucleophilic HO 2 - . In this manner the efficiency of the roles of both species is maximised. Copyright © 2017 Elsevier Inc. All rights reserved.

Urbanization accelerates long-term salinization and alkalinization of fresh water

Science.gov (United States)

Kaushal, S.; Duan, S.; Doody, T.; Haq, S.; Smith, R. M.; Newcomer Johnson, T. A.; Delaney Newcomb, K.; Gorman, J. K.; Bowman, N.; Mayer, P. M.; Wood, K. L.; Belt, K.; Stack, W.

2017-12-01

Human dominated land-use increases transport a major ions in streams due to anthropogenic salts and accelerated weathering. We show long-term trends in calcium, magnesium, sodium, alkalinity, and hardness over 50 years in the Baltimore metropolitan region and elsewhere. We also examine how major ion concentrations have increased significantly with impervious surface cover in watersheds across land use. Base cations show strong relationships with acid anions, which illustrates the coupling of major biogeochemical cycles in urban watersheds over time. Longitudinal patterns in major ions can also show increasing trends from headwaters to coastal waters, which suggests coupled biogeochemical cycles over space. We present new results from manipulative experiments and long-term monitoring across different urban regions regarding patterns and processes of salinization and alkalinization. Overall, our work demonstrates that urbanization dramatically increases major ions, ionic strength, and pH over decades from headwaters to coastal waters, which impacts the integrity of aquatic life, infrastructure, drinking water, and coastal ocean alkalinization.

Structural and Dynamical Properties of Alkaline Earth Metal Halides in Supercritical Water: Effect of Ion Size and Concentration.

Science.gov (United States)

Keshri, Sonanki; Tembe, B L

2017-11-22

Constant temperature-constant pressure molecular dynamics simulations have been performed for aqueous alkaline earth metal chloride [M 2+ -Cl - (M = Mg, Ca, Sr, and Ba)] solutions over a wide range of concentrations (0.27-5.55 m) in supercritical (SC) and ambient conditions to investigate their structural and dynamical properties. A strong influence of the salt concentration is observed on the ion-ion pair correlation functions in both ambient and SC conditions. In SC conditions, significant clustering is observed in the 0.27 m solution, whereas the reverse situation is observed at room temperature and this is also supported by the residence times of the clusters. The concentration and ion size (cation size) seem to have opposite effects on the average number of hydrogen bonds. The simulation results show that the self-diffusion coefficients of water, cations, and the chloride ion increase with increasing temperature, whereas they decrease with increasing salt concentration. The cluster size distribution shows a strong density dependence in both ambient and SC conditions. In SC conditions, cluster sizes display a near-Gaussian distribution, whereas the distribution decays monotonically in ambient conditions.

Stability Modification of SPR Silver Nano-Chips by Alkaline Condensation of Aminopropyltriethoxysilane

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M. Ghorbanpour

2015-04-01

Full Text Available The Silver SPR chip was modified by alkaline-silane condensation with aminopropyltriethoxysilane (APTES in NaOH aqueous solution at different times. Silver sputtered slides coated with APTES were immersed in NaOH solution, enabling us to produce silver surfaces homogeneously covered with APTES. The surface properties of grafted APTES on sputtered silver surface as a occasion of time were studied using SPR analysis, AFM and contact angle measurement. The mechanical and chemical stability of samples was assayed by tape test and NaCl test. The answers show that hydrolysis and condensation of APTES are activated in alkaline solution and lead to formation of a protective APTES layer on the surface of silver. The morphology of APTES on silver surface is a function of coverage density that is altered by changing time. At short times (< 30 min, APTES molecules physically adsorb to the surface leads to weak protection. At higher condensation times, APTES molecules chemically bond to the surface and each other leads to better protection.

The effect of high pH alkaline solutions on the mineral stability of the Boom Clay - Batch experiments at 60 deg. C

International Nuclear Information System (INIS)

Honty, M.; De Craen, M.; Wang, L.; Madejova, J.; Czimerova, A.; Pentrak, M.; Stricek, I.; Van Geet, M.

2010-01-01

Boom Clay is currently viewed as a reference host formation for studies on deep geological disposal of radioactive waste in Belgium. The interactions between bulk rock Boom Clay and 0.1 M KOH, 0.1 M NaOH, 0.1 M Ca(OH) 2 , young cement water and evolved cement water solutions, ranging in pH from 12.5 to 13.2, were examined as static batch experiments at 60 deg. C to simulate alkaline plume perturbations, which are expected to occur in the repository due to the presence of concrete. Both liquids and solids were investigated at specific times between 90 and 510 days in order to control the elemental budget and to search for potential mineralogical alterations. Also, the clay fraction was separated from the whole-rock Boom Clay at the end of each run and characterized for its mineralogical composition. Thereby, the importance of the mineral matrix to buffer the alkaline attack and the role of organic matter to protect clay minerals were also addressed. The results indicate that the degree of geochemical perturbation in Boom Clay is dependent on the initial pH of the applied solution together with the nature of the major cation in the reactant fluids. The higher the initial pH of the media, the stronger its interaction with Boom Clay. No major non-clay mineralogical alteration of the Boom Clay was detected, but dissolution of kaolinite, smectite and illite occurred within the studied experimental conditions. The dissolution of clays is accompanied by the decrease in the layer charge, followed by a decrease in the cation-exchange capacity. The highest TOC values coincide with the highest total elemental concentrations in the leachates, and correspondingly, the highest dissolution degree. However, no quantitative link could be established between the degree of organic matter decomposition and clay dissolution.

Alkaline elution of DNA from mammalian cells on cellulose triacetate filters

International Nuclear Information System (INIS)

Moss, A.J. Jr.; Nagle, W.A.; Henle, K.J.; Prior, R.M.

1984-01-01

The alkaline elution technique is widely used for the estimation of cellular DNA damage because of its sensitivity in the biologically relevant dose range. The authors have extended the original studies and provide additional characterization of the cellulose triacetate alkaline elution method. This filter material permits the elution of approximately 80 percent of cellular DNA from untreated V79 cells. the total radioactivity in the system was compartmentalized with respect to 1) lysing solution, 2) washing solution, 3) elution fractions, and 4) membrane retained activity. In these studies [/sup 3/H]-thymidine labeled untreated internal control cells were co-eluted with X-irradiated [/sup 14/C]-thymidine labeled cells. For the estimation of DNA damage, elution profiles for treated cells were directly compared with untreated internal control cells. The quantity of DNA eluting in excess of the labeled internal control per fraction is directly proportional to the extent of DNA damage in the treated sample. Using the technique the necessity of an irradiated internal control is eliminated

Activation of Alkaline Irrigation Fluids in Endodontics

Directory of Open Access Journals (Sweden)

Laurence J. Walsh

2017-10-01

Full Text Available In conventional endodontic treatment, alkaline solutions of sodium hypochlorite (NaOCl and ethylenediaminetetraacetic acid (EDTA are used in combination to disinfect the root canal system and to eliminate debris and smear layers. An important concept that has emerged over recent years is the use of active physical methods for agitating these fluids to improve their penetration within areas that are not reached by endodontic instruments and to accelerate the chemical actions of these alkaline fluids against planktonic microorganisms, biofilms, soft tissue remnants and smear layers. Ultrasonic agitation and more recently pulsed lasers have emerged as two promising methods for activating endodontic irrigation fluids. Ultrasonic agitation with piezoelectric devices employs a moving tip, while laser agitation uses a stationary tip. Both methods cause cavitation, followed by implosions and shear forces which assist with debridement. Fluid streaming further enhances the activity of the fluids. While agitation enhances performance of irrigants, extrusion of fluids from the root canal during activation is a hazard that must be controlled.

Use of polysulfides of alkali and alkaline-earth metals to obtain highly dispersed sulfur

International Nuclear Information System (INIS)

Massalimov, I.A.; Vikhareva, I.N.; Kireeva, M.S.

2008-01-01

Possibilities of obtaining polysulfides of alkali and alkaline earth metals (M is Na, K, Ca, Sr, Ba) in aqueous solutions were considered. The composition of the polysulfides and their concentration in solutions were found. The efficiencies of application of highly dispersed sulfur, produced from calcium polysulfide, and colloid sulfur as a fungicide were compared [ru

Strong pairing approximation in comparison with the exact solutions to the pairing Hamiltonian

Directory of Open Access Journals (Sweden)

Lunyov A.V.

2016-01-01

Full Text Available Results of the Strong Pairing Approximation (SPA as a method with the exact particle number conservation are compared with those of the quasiparticle method (QM. It is shown that SPA comes to the same equations as QM for the gap parameter, chemical potential and one- and two-quasiparticle states. Calculations are performed for 14864Gd84 as an example, and compared with the exact solutions to the pairing Hamiltonian.

n-Type Conductivity of Cu2O Thin Film Prepared in Basic Aqueous Solution Under Hydrothermal Conditions

Science.gov (United States)

Ursu, Daniel; Miclau, Nicolae; Miclau, Marinela

2018-03-01

We report for the first time in situ hydrothermal synthesis of n-type Cu2O thin film using strong alkaline solution. The use of copper foil as substrate and precursor material, low synthesis temperature and short reaction time represent the arguments of a new, simple, inexpensive and high field synthesis method for the preparation of n-type Cu2O thin film. The donor concentration of n-type Cu2O thin film obtained at 2 h of reaction time has increased two orders of magnitude than previous reported values. We have demonstrated n-type conduction in Cu2O thin film prepared in strong alkaline solution, in the contradiction with the previous works. Based on experimental results, the synthesis mechanism and the origin of n-type photo-responsive behavior of Cu2O thin film were discussed. We have proposed that the unexpected n-type character could be explained by H doping of Cu2O thin film in during of the hydrothermal synthesis that caused the p-to-n conductivity-type conversion. Also, this work raises new questions about the origin of n-type conduction in Cu2O thin film, the influence of the synthesis method on the nature of the intrinsic defects and the electrical conduction behavior.

Chemically durable polymer electrolytes for solid-state alkaline water electrolysis

Science.gov (United States)

Park, Eun Joo; Capuano, Christopher B.; Ayers, Katherine E.; Bae, Chulsung

2018-01-01

Generation of high purity hydrogen using electrochemical splitting of water is one of the most promising methods for sustainable fuel production. The materials to be used as solid-state electrolytes for alkaline water electrolyzer require high thermochemical stability against hydroxide ion attack in alkaline environment during the operation of electrolysis. In this study, two quaternary ammonium-tethered aromatic polymers were synthesized and investigated for anion exchange membrane (AEM)-based alkaline water electrolyzer. The membranes properties including ion exchange capacity (IEC), water uptake, swelling degree, and anion conductivity were studied. The membranes composed of all C-C bond polymer backbones and flexible side chain terminated by cation head groups exhibited remarkably good chemical stability by maintaining structural integrity in 1 M NaOH solution at 95 °C for 60 days. Initial electrochemical performance and steady-state operation performance were evaluated, and both membranes showed a good stabilization of the cell voltage during the steady-state operation at the constant current density at 200 mA/cm2. Although both membranes in current form require improvement in mechanical stability to afford better durability in electrolysis operation, the next generation AEMs based on this report could lead to potentially viable AEM candidates which can provide high electrolysis performance under alkaline operating condition.

Structural and thermal characterization of hemicelluloses isolated by organic solvents and alkaline solutions from Tamarix austromongolica.

Science.gov (United States)

Sun, Yong-Chang; Wen, Jia-Long; Xu, Feng; Sun, Run-Cang

2011-05-01

Three organosolv and three alkaline hemicellulosic fractions were prepared from lignocellulosic biomass of the fast-growing shrub Tamarix austromongolica (Tamarix Linn.). Sugar analysis revealed that the organosolv-soluble fractions contained a higher content of glucose (33.7-6.5%) and arabinose (14.8-5.6%), and a lower content of xylose (62.2-54.8%) than the hemicellulosic fractions isolated with aqueous alkali solutions. A relatively high concentration of alkali resulted in a decreasing trend of the xylose/4-O-methyl-D-glucuronic acid ratio in the alkali-soluble fractions. The results of NMR analysis supported a major substituted structure based on a linear polymer of β-(1→4)-linked d-xylopyranosyl residues, having ramifications of α-L-arabinofuranose and 4-O-methyl-D-glucuronic acid residues monosubstituted at O-3 and O-2, respectively. Thermogravimetric analysis revealed that one step of major mass loss occurred between 200-400°C, as hemicelluloses devolatilized with total volatile yield of about 55%. It was found that organosolv-soluble fractions are more highly ramified, and showed a higher thermal stability than the alkali-soluble fractions. Copyright © 2011 Elsevier Ltd. All rights reserved.

Porous boron doped diamonds as metal-free catalysts for the oxygen reduction reaction in alkaline solution

Science.gov (United States)

Suo, Ni; Huang, Hao; Wu, Aimin; Cao, Guozhong; Hou, Xiaoduo; Zhang, Guifeng

2018-05-01

Porous boron doped diamonds (BDDs) were obtained on foam nickel substrates with a porosity of 80%, 85%, 90% and 95% respectively by hot filament chemical vapor deposition (HFCVD) technology. Scanning electron microscopy (SEM) reveals that uniform and compact BDDs with a cauliflower-like morphology have covered the overall frame of the foam nickel substrates. Raman spectroscopy shows that the BDDs have a poor crystallinity due to heavily doping boron. X-ray photoelectron spectroscopy (XPS) analysis effectively demonstrates that boron atoms can be successfully incorporated into the crystal lattice of diamonds. Electrochemical measurements indicate that the oxygen reduction potential is unaffected by the specific surface area (SSA), and both the onset potential and the limiting diffusion current density are enhanced with increasing SSA. It is also found that the durability and methanol tolerance of the boron doped diamond catalysts are attenuated as the increasing of SSA. The SSA of the catalyst is directly proportional to the oxygen reduction activity and inversely to the durability and methanol resistance. These results provide a reference to the application of porous boron doped diamonds as potential cathodic catalysts for the oxygen reduction reaction in alkaline solution by adjusting the SSA.

Seeking effective dyes for a mediated glucose-air alkaline battery/fuel cell

Science.gov (United States)

Eustis, Ross; Tsang, Tsz Ming; Yang, Brigham; Scott, Daniel; Liaw, Bor Yann

2014-02-01

A significant level of power generation from an abiotic, air breathing, mediated reducing sugar-air alkaline battery/fuel cell has been achieved in our laboratories at room temperature without complicated catalysis or membrane separation in the reaction chamber. Our prior studies suggested that mass transport limitation by the mediator is a limiting factor in power generation. New and effective mediators were sought here to improve charge transfer and power density. Forty-five redox dyes were studied to identify if any can facilitate mass transport in alkaline electrolyte solution; namely, by increasing the solubility and mobility of the dye, and the valence charge carried per molecule. Indigo dyes were studied more closely to understand the complexity involved in mass transport. The viability of water-miscible co-solvents was also explored to understand their effect on solubility and mass transport of the dyes. Using a 2.0 mL solution, 20% methanol by volume, with 100 mM indigo carmine, 1.0 M glucose and 2.5 M sodium hydroxide, the glucose-air alkaline battery/fuel cell attained 8 mA cm-2 at short-circuit and 800 μW cm-2 at the maximum power point. This work shall aid future optimization of mediated charge transfer mechanism in batteries or fuel cells.

Mineralogical, petrological and geochemical aspects of alkaline and alkaline-carbonatite associations from Brazil

Science.gov (United States)

Morbidelli, L.; Gomes, C. B.; Beccaluva, L.; Brotzu, P.; Conte, A. M.; Ruberti, E.; Traversa, G.

1995-12-01

A general description of Mesozoic and Tertiary (Fortaleza) Brazilian alkaline and alkaline-carbonatite districts is presented with reference to mineralogy, petrology, geochemistry and geochronology. It mainly refers to scientific results obtained during the last decade by an Italo-Brazilian research team. Alkaline occurrences are distributed across Brazilian territory from the southern (Piratini, Rio Grande do Sul State) to the northeastern (Fortaleza, Ceará State) regions and are mainly concentrated along the borders of the Paraná Basin generally coinciding with important tectonic lineaments. The most noteworthy characteristics of these alkaline and alkaline-carbonatite suites are: (i) prevalence of intrusive forms; (ii) abundance of cumulate assemblages (minor dunites, frequent clinopyroxenites and members of the ijolite series) and (iii) abundance of evolved rock-types. Many data demonstrate that crystal fractionation was the main process responsible for magma evolution of all Brazilian alkaline rocks. A hypothesis is proposed for the genesis of carbonatite liquids by immiscibility processes. The incidence of REE and trace elements for different major groups of lithotypes, belonging both to carbonatite-bearing and carbonatite-free districts, are documented. Sr and preliminary Nd isotopic data are indicative of a mantle origin for the least evolved magmas of all the studied occurrences. Mantle source material and melting models for the generation of the Brazilian alkaline magma types are also discussed.

Study of the alloying additives and alkaline zincate solution effects on the commercial aluminum as galvanic anode for use in alkaline batteries

International Nuclear Information System (INIS)

Rashvand avei, M.; Jafarian, M.; Moghanni Bavil Olyaei, H.; Gobal, F.; Hosseini, S.M.; Mahjani, M.G.

2013-01-01

The corrosion behavior of different grades of commercial aluminum such as AA1040, AA5083, AA6060 and AA7075 in ZnO-containing 4 M NaOH has been determined by using open circuit potential-time measurements (OCP), galvanostatic and potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). The results of scanning electron microscopy (SEM) and energy dispersive analysis of X-ray (EDAX) reveal that ZnO produces the inhibition effect by the formation of a zinc-containing deposit layer on the surface of aluminum electrodes. Although the influence of zincating on the performance of aluminum alloys and considering the amount of alloying elements such as zinc, magnesium and manganese in AA7075 and AA5083 alloys is much more than AA6060 one, the AA6060 aluminum exhibits negligible corrosion rate. Alloying aluminum with other elements and modifying the composition of the electrolyte is a necessary condition for reducing the self-corrosion of the aluminum anodes, whereas the proportion of the amount of additive elements is sufficient and important condition. As AA6060 with a low amount of Zn and Mg, but the high value of the ratio of (Mg/Zn) content (>400) can serve as a good galvanic anode in the alkaline media. - Highlights: • Decreasing the corrosion rate of tested alloys in 4 M NaOH solution specially AA6060. • Lowering the extent of anodic polarization at a current density of 50 mA cm −2 . • High inhibitor efficiency about 97% for AA6060

Study of the alloying additives and alkaline zincate solution effects on the commercial aluminum as galvanic anode for use in alkaline batteries

Energy Technology Data Exchange (ETDEWEB)

Rashvand avei, M. [Department of Chemistry, K.N. Toosi University of Technology, P.O. Box 15875-4416, Tehran (Iran, Islamic Republic of); Jafarian, M., E-mail: mjafarian@kntu.ac.ir [Department of Chemistry, K.N. Toosi University of Technology, P.O. Box 15875-4416, Tehran (Iran, Islamic Republic of); Moghanni Bavil Olyaei, H. [Department of Chemistry, K.N. Toosi University of Technology, P.O. Box 15875-4416, Tehran (Iran, Islamic Republic of); Gobal, F. [Department of Chemistry, Sharif University of Technology, P.O. Box 11365-8516, Tehran (Iran, Islamic Republic of); Hosseini, S.M. [Jahad Organization – Science and Technology Center, Tehran (Iran, Islamic Republic of); Mahjani, M.G. [Department of Chemistry, K.N. Toosi University of Technology, P.O. Box 15875-4416, Tehran (Iran, Islamic Republic of)

2013-12-16

The corrosion behavior of different grades of commercial aluminum such as AA1040, AA5083, AA6060 and AA7075 in ZnO-containing 4 M NaOH has been determined by using open circuit potential-time measurements (OCP), galvanostatic and potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). The results of scanning electron microscopy (SEM) and energy dispersive analysis of X-ray (EDAX) reveal that ZnO produces the inhibition effect by the formation of a zinc-containing deposit layer on the surface of aluminum electrodes. Although the influence of zincating on the performance of aluminum alloys and considering the amount of alloying elements such as zinc, magnesium and manganese in AA7075 and AA5083 alloys is much more than AA6060 one, the AA6060 aluminum exhibits negligible corrosion rate. Alloying aluminum with other elements and modifying the composition of the electrolyte is a necessary condition for reducing the self-corrosion of the aluminum anodes, whereas the proportion of the amount of additive elements is sufficient and important condition. As AA6060 with a low amount of Zn and Mg, but the high value of the ratio of (Mg/Zn) content (>400) can serve as a good galvanic anode in the alkaline media. - Highlights: • Decreasing the corrosion rate of tested alloys in 4 M NaOH solution specially AA6060. • Lowering the extent of anodic polarization at a current density of 50 mA cm{sup −2}. • High inhibitor efficiency about 97% for AA6060.

Summary technical report on the electrochemical treatment of alkaline nuclear wastes

International Nuclear Information System (INIS)

Hobbs, D.T.

1994-01-01

This report summarizes the laboratory studies investigating the electrolytic treatment of alkaline solutions carried out under the direction of the Savannah River Technology Center from 1985-1992. Electrolytic treatment has been demonstrated at the laboratory scale to be feasible for the destruction of nitrate and nitrite and the removal of radioactive species such as 99 Tc and 106 Ru from Savannah River Site (SRS) decontaminated salt solution and other alkaline wastes. The reaction rate and current efficiency for the removal of these species are dependent on cell configuration, electrode material, nature of electrode surface, waste composition, current density, and temperature. Nitrogen, ammonia, and nitrous oxide have been identified as the nitrogen-containing reaction products from the electrochemical reduction of nitrate and nitrite under alkaline conditions. The reaction mechanism for the reduction is very complex. Voltammetric studies indicated that the electrode reactions involve surface phenomena and are not necessarily mass transfer controlled. In an undivided cell, results suggest an electrocatalytic role for oxygen via the generation of the superoxide anion. In general, more efficient reduction of nitrite and nitrate occurs at cathode materials with higher overpotentials for hydrogen evolution. Nitrate and nitrite destruction has also been demonstrated in engineering-scale flow reactors. In flow reactors, the nitrate/nitrite destruction efficiency is improved with an increase in the current density, temperature, and when the cell is operated in a divided cell configuration. Nafion reg-sign cation exchange membranes have exhibited good stability and consistent performance as separators in the divided-cell tests. The membranes were also shown to be unaffected by radiation at doses approximating four years of cell operation in treating decontaminated salt solution

Hydrogen generation by aluminum corrosion in aqueous alkaline solutions of inorganic promoters: The AlHidrox process

International Nuclear Information System (INIS)

Macanas, Jorge; Soler, Lluis; Candela, Angelica Maria; Munoz, Maria; Casado, Juan

2011-01-01

The research of alternative processes to obtain clean fuels has become a main issue because of the concerns related to the current energy system, both from economical and environmental points of view. Hydrogen storage and production methods are being investigated for stationary and portable applications. Up to now, a significant part of H 2 production on demand was thought to be fulfilled by using chemical hydrides, but recent studies have proved the limitations of this approach. Conversely, H 2 production based in the corrosion of light metals in water solutions is an interesting alternative. Among all of them, Al is probably the most adequate metal for energetic purposes due to its high electron density and oxidation potential. But concerning H 2 production from Al corrosion in water, a major issue remains unsolved: metal passivation due to the formation of Al(OH) 3 inhibits H 2 evolution. In this work we show the last results obtained for the generation of H 2 from water using Al powder using diverse alkaline solutions. It is confirmed that corrosion is not affected solely by the solution pH but also by the nature of the ionic species found in the aqueous medium. Moreover, we describe the AlHidrox process, which minimizes Al passivation under mild conditions by the addition of different inorganic salts as corrosion promoters, allowing 100% yields and flow rates up to 2.9 L/min per gram of Al. The feasibility of the process has been regarded in terms of stability (by conducting several successive runs) and self-initiation without an external heating. -- Highlights: → The AlHidrox process minimizes Al passivation by the addition of inorganic salts. → Al corrosion to produce H 2 greatly depends on the nature of the dissolved species. → The maximum flow achieved was 2.9 dm 3 H 2 min -1 .per gram of Al using Fe 2 (SO 4 ) 3 . → We found conditions to start up H 2 generation without external energy input.

Alkaline sodium borohydride gel as a hydrogen source for PEMFC or an energy carrier for NaBH 4-air battery

Science.gov (United States)

Liu, B. H.; Li, Z. P.; Chen, L. L.

In this preliminary study, we tried to use sodium polyacrylate as the super absorbent polymer to form alkaline NaBH 4 gel and explored its possibilities for borohydride hydrolysis and borohydride electro-oxidation. It was found that the absorption capacity of sodium polyacrylate decreased with increasing NaBH 4 concentration. The formed gel was rather stable in the sealed vessel but tended to slowly decompose in open air. Hydrogen generation from the gel was carried out using CoCl 2 catalyst precursor solutions. Hydrogen generation rate from the alkaline NaBH 4 gel was found to be higher and impurities in hydrogen were less than that from the alkaline NaBH 4 solution. The NaBH 4 gel also successfully powered a NaBH 4-air battery.

Silica-poor, mafic alkaline lavas from ocean islands and continents

Indian Academy of Sciences (India)

Strongly silica-poor (ne-normative), mafic alkaline lavas generally represented by olivine nephelinites, nephelinites, melilitites, and olivine melilitites have erupted at various locations during Earth's history. On the basis of bulk-rock Mg#, high concentrations of Na2O, TiO2, and K2O, and trace element geochemistry, it has ...

Overestimation of organic phosphorus in wetland soils by alkaline extraction and molybdate colorimetry.

Science.gov (United States)

Turner, Benjamin L; Newman, Susan; Reddy, K Ramesh

2006-05-15

Accurate information on the chemical nature of soil phosphorus is essential for understanding its bioavailability and fate in wetland ecosystems. Solution phosphorus-31 nuclear magnetic resonance (31P NMR) spectroscopy was used to assess the conventional colorimetric procedure for phosphorus speciation in alkaline extracts of organic soils from the Florida Everglades. Molybdate colorimetry markedly overestimated organic phosphorus by between 30 and 54% compared to NMR spectroscopy. This was due in large part to the association of inorganic phosphate with organic matter, although the error was exacerbated in some samples by the presence of pyrophosphate, an inorganic polyphosphate that is not detected by colorimetry. The results have important implications for our understanding of phosphorus biogeochemistry in wetlands and suggest that alkaline extraction and solution 31p NMR spectroscopy is the only accurate method for quantifying organic phosphorus in wetland soils.

Organic Control of Dioctahedral and Trioctahedral Clay Formation in an Alkaline Soil System in the Pantanal Wetland of Nhecolândia, Brazil.

Science.gov (United States)

Barbiero, Laurent; Berger, Gilles; Rezende Filho, Ary T; Meunier, Jean-François; Martins-Silva, Elisângela R; Furian, Sonia

2016-01-01

Recent studies have focused on the formation of authigenic clays in an alkaline soil system surrounding lakes of the Nhecolândia region, Pantanal wetland. The presence of trioctahedral Mg-smectites (stevensite and saponite types), which requires low Al and Fe contents in the soil solution for its formation, contrasts with the neoformation of dioctahedral Fe-mica (glauconite, and Fe-illite), which instead requires solutions relatively enriched in Al and Fe. This study aims to understand the conditions of co-existence of both, Mg-smectite and Fe-mica a common clay association in former or modern alkaline soil systems and sediments. The study was carried out along an alkaline soil catena representative of the region. The soil organization revealed that Mg-smectite occur in top soil close to the lake, whereas Fe-mica dominate in the clay fraction of deeper greenish horizons a few meters apart. We propose here that this spatial distribution is controlled by the lateral transfer of Fe and Al with organic ligands. Alkaline organic rich solutions (DOC up to 738 mg L-1) collected in the watertable were centrifuged and filtered through membranes of decreasing pore size (0.45 μm, 0.2 μm, 30 KDa, 10 KDa, 3 KDa) to separate colloidal and dissolved fractions. Fe, Al, Si, Mg and K were analysed for each fraction. Although the filtration had no influence on Si and K contents, almost 90% of Fe (up to 2.3 mg L-1) and Al (up to 7 mg L-1) are retained at the first cutoff threshold of 0.45μm. The treatment of the same solutions by oxygen peroxide before filtration shows that a large proportion of Fe and Al were bonded to organic colloids in alkaline soil solution at the immediate lake border, allowing Mg-smectite precipitation. The fast mineralization of the organic matter a few meters apart from the lake favors the release of Fe and Al necessary for Fe-mica neoformation. In comparison with chemical and mineralogical characteristics of alkaline environments described in the

Organic Control of Dioctahedral and Trioctahedral Clay Formation in an Alkaline Soil System in the Pantanal Wetland of Nhecolândia, Brazil

Science.gov (United States)

Meunier, Jean-François; Martins-Silva, Elisângela R.; Furian, Sonia

2016-01-01

Recent studies have focused on the formation of authigenic clays in an alkaline soil system surrounding lakes of the Nhecolândia region, Pantanal wetland. The presence of trioctahedral Mg-smectites (stevensite and saponite types), which requires low Al and Fe contents in the soil solution for its formation, contrasts with the neoformation of dioctahedral Fe-mica (glauconite, and Fe-illite), which instead requires solutions relatively enriched in Al and Fe. This study aims to understand the conditions of co-existence of both, Mg-smectite and Fe-mica a common clay association in former or modern alkaline soil systems and sediments. The study was carried out along an alkaline soil catena representative of the region. The soil organization revealed that Mg-smectite occur in top soil close to the lake, whereas Fe-mica dominate in the clay fraction of deeper greenish horizons a few meters apart. We propose here that this spatial distribution is controlled by the lateral transfer of Fe and Al with organic ligands. Alkaline organic rich solutions (DOC up to 738 mg L-1) collected in the watertable were centrifuged and filtered through membranes of decreasing pore size (0.45 μm, 0.2 μm, 30 KDa, 10 KDa, 3 KDa) to separate colloidal and dissolved fractions. Fe, Al, Si, Mg and K were analysed for each fraction. Although the filtration had no influence on Si and K contents, almost 90% of Fe (up to 2.3 mg L-1) and Al (up to 7 mg L-1) are retained at the first cutoff threshold of 0.45μm. The treatment of the same solutions by oxygen peroxide before filtration shows that a large proportion of Fe and Al were bonded to organic colloids in alkaline soil solution at the immediate lake border, allowing Mg-smectite precipitation. The fast mineralization of the organic matter a few meters apart from the lake favors the release of Fe and Al necessary for Fe-mica neoformation. In comparison with chemical and mineralogical characteristics of alkaline environments described in the

Organic Control of Dioctahedral and Trioctahedral Clay Formation in an Alkaline Soil System in the Pantanal Wetland of Nhecolândia, Brazil.

Directory of Open Access Journals (Sweden)

Laurent Barbiero

Full Text Available Recent studies have focused on the formation of authigenic clays in an alkaline soil system surrounding lakes of the Nhecolândia region, Pantanal wetland. The presence of trioctahedral Mg-smectites (stevensite and saponite types, which requires low Al and Fe contents in the soil solution for its formation, contrasts with the neoformation of dioctahedral Fe-mica (glauconite, and Fe-illite, which instead requires solutions relatively enriched in Al and Fe. This study aims to understand the conditions of co-existence of both, Mg-smectite and Fe-mica a common clay association in former or modern alkaline soil systems and sediments. The study was carried out along an alkaline soil catena representative of the region. The soil organization revealed that Mg-smectite occur in top soil close to the lake, whereas Fe-mica dominate in the clay fraction of deeper greenish horizons a few meters apart. We propose here that this spatial distribution is controlled by the lateral transfer of Fe and Al with organic ligands. Alkaline organic rich solutions (DOC up to 738 mg L-1 collected in the watertable were centrifuged and filtered through membranes of decreasing pore size (0.45 μm, 0.2 μm, 30 KDa, 10 KDa, 3 KDa to separate colloidal and dissolved fractions. Fe, Al, Si, Mg and K were analysed for each fraction. Although the filtration had no influence on Si and K contents, almost 90% of Fe (up to 2.3 mg L-1 and Al (up to 7 mg L-1 are retained at the first cutoff threshold of 0.45μm. The treatment of the same solutions by oxygen peroxide before filtration shows that a large proportion of Fe and Al were bonded to organic colloids in alkaline soil solution at the immediate lake border, allowing Mg-smectite precipitation. The fast mineralization of the organic matter a few meters apart from the lake favors the release of Fe and Al necessary for Fe-mica neoformation. In comparison with chemical and mineralogical characteristics of alkaline environments described

Carbon nitride nanotube as a sensor for alkali and alkaline earth cations

Energy Technology Data Exchange (ETDEWEB)

Beheshtian, Javad [Department of Chemistry, Shahid Rajaee Teacher Training University, P.O. Box: 16875-163, Tehran (Iran, Islamic Republic of); Baei, Mohammad T. [Department of Chemistry, Azadshahr Branch, Islamic Azad University, Azadshahr, Golestan (Iran, Islamic Republic of); Bagheri, Zargham [Physics Group, Science Department, Islamic Azad University, Islamshahr Branch, P.O. Box: 33135-369, Islamshahr, Tehran (Iran, Islamic Republic of); Peyghan, Ali Ahmadi, E-mail: ahmadi.iau@gmail.com [Young Researchers Club, Islamic Azad University, Islamshahr Branch, Tehran (Iran, Islamic Republic of)

2013-01-01

Highlights: Black-Right-Pointing-Pointer Adsorption of alkali and alkaline earth cations on a CN nanotube studied by DFT. Black-Right-Pointing-Pointer The alkaline cation adsorption may raise potential barrier of the electron emission. Black-Right-Pointing-Pointer The tube may act as a sensor in the presence of alkali and alkaline cations. - Abstract: Adsorption of several alkali (Li{sup +}, Na{sup +}, and K{sup +}) and alkaline earth (Be{sup 2+}, Mg{sup 2+}, and Ca{sup 2+}) cations on the surface of a zigzag (9, 0) carbon nitride nanotube has been investigated using density functional theory. It has been found that almost all of the cations prefer to be strongly chemisorbed at the center of porous site of the tube surface. The adsorption of alkaline cations much more influences the electronic properties of the tube, in comparison with the alkali ones, so that it is transformed from an intrinsic semiconductor with HOMO/LUMO energy gap of 4.02 eV to extrinsic p-type one with the gap of 0.54-1.94 eV. The alkaline cation adsorption may significantly raise potential barrier of the electron emission from the tube surface, hence impeding the field emission. It has been also concluded that the electrical sensitivity of the tube toward the cations may be in the order: Be{sup 2+} Much-Greater-Than Mg{sup 2+} Much-Greater-Than Ca{sup 2+} Much-Greater-Than Li{sup +} {approx} Na{sup +} {approx} K{sup +}.

Reduction of nitrobenzene with alkaline ascorbic acid: Kinetics and pathways

Energy Technology Data Exchange (ETDEWEB)

Liang, Chenju, E-mail: cliang@nchu.edu.tw [Department of Environmental Engineering, National Chung Hsing University 250, Kuo-kuang Road, Taichung 402, Taiwan (China); Lin, Ya-Ting [Department of Environmental Engineering, Chung Yuan Christian University, 200 Chung Pei Road, Chung Li District, Taoyuan City 320, Taiwan (China); Shiu, Jia-Wei [Department of Environmental Engineering, National Chung Hsing University 250, Kuo-kuang Road, Taichung 402, Taiwan (China)

2016-01-25

Highlights: • Alkaline ascorbic acid (a.k.a. vitamin C) is capable of reductively degrading NB. • The pH above the pK{sub a2} of ascorbic acid increases reductive electron transfer to NB. • The rate equation for the reactions between NB and AA is determined. • NSB, AZOXY, and AZO are identified as intermediates and aniline as a final product. • Alkaline pH is essential for AA remediation of NB contaminated soils. - Abstract: Alkaline ascorbic acid (AA) exhibits the potential to reductively degrade nitrobenzene (NB), which is the simplest of the nitroaromatic compounds. The nitro group (NO{sub 2}{sup −}) of NB has a +III oxidation state of the N atom and tends to gain electrons. The effect of alkaline pH ranging from 9 to 13 was initially assessed and the results demonstrated that the solution pH, when approaching or above the pK{sub a2} of AA (11.79), would increase reductive electron transfer to NB. The rate equation for the reactions between NB and AA at pH 12 can be described as r = ((0.89 ± 0.11) × 10{sup −4} mM{sup 1−(a} {sup +} {sup b)} h{sup −1}) × [NB]{sup a} {sup =} {sup 1.35} {sup ±} {sup 0.10}[AA]{sup b} {sup =} {sup 0.89} {sup ±} {sup 0.01}. The GC/MS analytical method identified nitrosobenzene, azoxybenzene, and azobenzene as NB reduction intermediates, and aniline (AN) as a final product. These experimental results indicate that the alkaline AA reduction of NB to AN mainly proceeds via the direct route, consisting of a series of two-electron or four-electron transfers, and the condensation reaction plays a minor route. Preliminary evaluation of the remediation of spiked NB contaminated soils revealed that maintenance of alkaline pH and a higher water to soil ratio are essential for a successful alkaline AA application.

An inorganic CO2 diffusion and dissolution process explains negative CO2 fluxes in saline/alkaline soils

Science.gov (United States)

Ma, Jie; Wang, Zhong-Yuan; Stevenson, Bryan A.; Zheng, Xin-Jun; Li, Yan

2013-01-01

An ‘anomalous' negative flux, in which carbon dioxide (CO2) enters rather than is released from the ground, was studied in a saline/alkaline soil. Soil sterilization disclosed an inorganic process of CO2 dissolution into (during the night) and out of (during the day) the soil solution, driven by variation in soil temperature. Experimental and modeling analysis revealed that pH and soil moisture were the most important determinants of the magnitude of this inorganic CO2 flux. In the extreme cases of air-dried saline/alkaline soils, this inorganic process was predominant. While the diurnal flux measured was zero sum, leaching of the dissolved inorganic carbon in the soil solution could potentially effect net carbon ecosystem exchange. This finding implies that an inorganic module should be incorporated when dealing with the CO2 flux of saline/alkaline land. Neglecting this inorganic flux may induce erroneous or misleading conclusions in interpreting CO2 fluxes of these ecosystems. PMID:23778238

Use to titanium-treated zeolite for plutonium, strontium, and cesium removal from West Valley alkaline wastes and sludge wash wastes

International Nuclear Information System (INIS)

Bray, L.A.; Hara, F.T.

1993-01-01

Zeolite (IONSIV IE-96) treated with a titanium (Ti) solution will extract traces of plutonium (Pu), strontium (Sr), and cesium (Cs) found in the West Valley Nuclear Services Co., Inc. (WVNS) alkaline supernatant and alkaline sludge water washes. Small ion exchange columns containing Ti-treated zeolite have been successfully tested at WVNS and Pacific Northwest Laboratory (PNL) for the removal of Pu. Full-scale ion exchange processing of sludge wash solution is now being developed at WVNS for use in FY 1992. Commercial manufacturing options for the production of the Ti-treated zeolite were investigated. The Ti-treated zeolite may have application at Hanford and at other U.S. Department of Energy (DOE) sites for the removal of low-level concentrations of Cs, Sr, and Pu from alkaline waste streams

Multiscale Alterations in Sugar Cane Bagasse and Straw Submitted to Alkaline Deacetylation

Energy Technology Data Exchange (ETDEWEB)

Lima, Cleilton S. [Brazilian Bioethanol Science and Technology Laboratory (CTBE), Brazilian Center for Research in Energy and Materials (CNPEM), 13083-970 Campinas, São Paulo, Brazil; Department of Biotechnology, Engineering College of Lorena, University of São Paulo, 12602-810 Lorena, São Paulo, Brazil; Rabelo, Sarita C. [Brazilian Bioethanol Science and Technology Laboratory (CTBE), Brazilian Center for Research in Energy and Materials (CNPEM), 13083-970 Campinas, São Paulo, Brazil; Ciesielski, Peter N. [Biosciences Center, National Renewable Energy Laboratory, 15013 Denver West Parkway, Golden, Colorado 80401, United States; Roberto, Inês C. [Department of Biotechnology, Engineering College of Lorena, University of São Paulo, 12602-810 Lorena, São Paulo, Brazil; Rocha, George J. M. [Department of Biotechnology, Engineering College of Lorena, University of São Paulo, 12602-810 Lorena, São Paulo, Brazil; Driemeier, Carlos [Brazilian Bioethanol Science and Technology Laboratory (CTBE), Brazilian Center for Research in Energy and Materials (CNPEM), 13083-970 Campinas, São Paulo, Brazil

2018-01-31

Alkaline deacetylation has emerged as a promising chemistry for pretreatments performed prior to enzymatic saccharification of lignocellulosic biomass. This process avoids complex pressurized reactors and opens new opportunities for lignin covalorization. In this work, we evaluate the chemical and morphological response of sugar cane bagasse and straw submitted to alkaline treatments. Alkaline solutions for deacetylation (0.4% w/w NaOH, 70 degrees C, 3 h) as well as proximal conditions (0.1-0.7% NaOH, 55-85 degrees C, 1-5 h) chosen by 23 experimental design were evaluated. The deacetylation treatment removes ~90% of the acetyl groups and 20-30% of the lignin from both bagasse and straw, while removal of ~20% of the xylan and glucan is observed in straw, but not in bagasse. Considering nanoscale structural alterations, neither cellulose cocrystallization (evaluated by X-ray diffraction) nor formation of lignin aggregates (evaluated by thermoporometric signature) are observed after the alkaline conditions, in contrast to observations after hydrothermal treatments. Furthermore, calorimetric thermoporometry as well as scanning and transmission electron microscopies show substantial introduction of nanoscale porosity and loosening of the tissue and cell wall structures, indicating desirable mechanical weakening and gains in enzyme accessibility. These results provide fundamental and practical knowledge for biorefineries based on alkaline deacetylation of sugar cane bagasse and straw.

Behavior of ellagitannins, gallic acid, and ellagic acid under alkaline conditions

Science.gov (United States)

Richard W. Hemingway; W.E. Hillis

1971-01-01

Examination of the rates of hydrolysis of different ellagitannins under conditions comparable with cold soda and alkaline-groundwood pulping processes showed that some ellagitannins are notably resistant to hydrolysis. The rate of hydrolysis was dependent upon the pH and tempemture of the solution and particularly upon the structure of the compound. Decarboxylation of...

Power ultrasound irradiation during the alkaline etching process of the 2024 aluminum alloy

Science.gov (United States)

Moutarlier, V.; Viennet, R.; Rolet, J.; Gigandet, M. P.; Hihn, J. Y.

2015-11-01

Prior to any surface treatment on an aluminum alloy, a surface preparation is necessary. This commonly consists in performing an alkaline etching followed by acid deoxidizing. In this work, the use of power ultrasound irradiation during the etching step on the 2024 aluminum alloy was studied. The etching rate was estimated by weight loss, and the alkaline film formed during the etching step was characterized by glow discharge optical emission spectrometry (GDOES) and scanning electron microscope (SEM). The benefit of power ultrasound during the etching step was confirmed by pitting potential measurement in NaCl solution after a post-treatment (anodizing).

Measurement of pH, alkalinity and acidity in ultra-soft waters

African Journals Online (AJOL)

drinie

2001-10-04

Oct 4, 2001 ... A blend composed of the raw water, sodium chloride (to increase conductivity), and standard bicarbonate (to increase buffering capacity) was titrated with standard strong acid in two pH regions: 6.3 pH < 4.0. In both methods, total alkalinity was determined using the latter set of points, ...

Geochemical features of the Cretaceous alkaline volcanics in the area of Morado hill, Jachal town, San Juan, Argentina

International Nuclear Information System (INIS)

Perez, L.

2010-01-01

This paper is about the alkaline volcanic rocks that crop out at the Morado hill located in the southern end of the Mogna ranges, which are part of the Eastern border of the pre mountain in the San Juan province, Argentina.The petrography and geochemistry study of the alkaline volcanics has allowed to classify them as tephrite basanite or basanite nephelinite, with strong alkaline chemical affinity, showing a characteristic composition of within plate geochemistry environment. The radimetric analysis, K-Ar data, has shown an average 90 ∓ 8 m.y. age for this rocks, (Cingolani et al. 1984) pointing out the Upper Cretaceous (lower section) stratigraphical position for the suite. The discussion of the results makes conspicuous the relationships of these alkaline rocks with others of the central and northwestern regions of the country that allowed to establish an alkaline petrographic province

Microstructure characteristic of ceramic coatings fabricated on magnesium alloys by micro-arc oxidation in alkaline silicate solutions

Energy Technology Data Exchange (ETDEWEB)

Guo, H.F. [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China)]. E-mail: Guohf@hit.edu.cn; An, M.Z. [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China)]. E-mail: mzan@hit.edu.cn; Huo, H.B. [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China); Xu, S. [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China); Wu, L.J. [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China)

2006-09-15

Micro-arc oxidation (MAO) of AZ31B magnesium alloys was studied in alkaline silicate solutions at constant applied current densities. The microstructure, phase composition and elemental distribution of ceramic coatings were investigated using scanning electron microscopy (SEM), X-ray diffraction (XRD) and energy-dispersive spectroscopy (EDX). There are two inflections in the voltage-time response, three regions were identifiable and each of the regions was almost linear. The pores with different shapes distributed all over the coating surface, the number of the pores was decreasing, while the diameter was apparently increasing with prolonged MAO treatment time. There were also cracks on the coating surface, resulting from the rapid solidification of the molten oxide. The ceramic coating was comprised of two layers, an outer loose layer and an inner dense layer. The ceramic coating was mainly composed of forsterite phase Mg{sub 2}SiO{sub 4} and MgO; the formation of MgO was similar to conversional anodizing technology, while formation of Mg{sub 2}SiO{sub 4} was attributed to a high temperature phase transformation reaction. Presence of Si and O indicated that the electrolyte components had intensively incorporated into coatings.

Strong cosmic censorship for solutions of the Einstein-Maxwell field equations with polarized Gowdy symmetry

Energy Technology Data Exchange (ETDEWEB)

Nungesser, Ernesto; Rendall, Alan D [Max-Planck-Institut fuer Gravitationsphysik, Albert-Einstein-Institut, Am Muehlenberg 1, 14476 Potsdam (Germany)

2009-05-21

A proof of strong cosmic censorship is presented for a class of solutions of the Einstein-Maxwell equations, those with polarized Gowdy symmetry. A key element of the argument is the observation that by means of a suitable choice of variables the central equations in this problem can be written in a form where they are identical to the central equations for general (i.e. non-polarized) vacuum Gowdy spacetimes. Using this, it is seen that the deep results of Ringstroem on strong cosmic censorship in the vacuum case have implications for the Einstein-Maxwell case. Working out the geometrical meaning of these analytical results leads to the main conclusion.

Strong cosmic censorship for solutions of the Einstein-Maxwell field equations with polarized Gowdy symmetry

International Nuclear Information System (INIS)

Nungesser, Ernesto; Rendall, Alan D

2009-01-01

A proof of strong cosmic censorship is presented for a class of solutions of the Einstein-Maxwell equations, those with polarized Gowdy symmetry. A key element of the argument is the observation that by means of a suitable choice of variables the central equations in this problem can be written in a form where they are identical to the central equations for general (i.e. non-polarized) vacuum Gowdy spacetimes. Using this, it is seen that the deep results of Ringstroem on strong cosmic censorship in the vacuum case have implications for the Einstein-Maxwell case. Working out the geometrical meaning of these analytical results leads to the main conclusion.

Separation of radionuclides from spent decontamination solutions and/or evaporator concentrates

International Nuclear Information System (INIS)

Sebesta, F.; John, J.; Rosikova, K.; Motl, A.

1999-01-01

Separation of radionuclides from spent alkaline decontamination solutions has been tested in model experiments with strontium separation from simulant solution. The composite absorbers tested included TiO-PAN and NaTiO-PAN materials (titanium dioxide or sodium titanate incorporated into a matrix of polyacrylonitrile binder). As an alkaline simulant, solution of 1 M NaOH + 1 M NaNO 3 + 10 -4 M Ca(NO 3 ) 2 + 10 -5 M Sr(NO 3 ) 2 spiked with a carrier-free 85 Sr tracer, was used. The experiments were performed at a flow rate of 12.5 BV/hr. Some experiments with real and simulant spent decontamination solutions are described

Volta potential of clad AA2024 aluminium after exposure to CeCl3 solution

International Nuclear Information System (INIS)

Andreatta, F.; Druart, M.-E.; Marin, E.; Cossement, D.; Olivier, M.-G.; Fedrizzi, L.

2014-01-01

Highlights: • Alkaline etch of clad AA2024 enhances precipitation of Ce compounds. • Exposure to CeCl 3 solution decreases Volta potential of alkaline etched substrate. • Ce compounds reduce the driving force for initiation of localized attack. - Abstract: AA2024 clad with AA1050 was immersed in CeCl 3 solution to promote deposition of cerium species. The deposition occurs on the entire sample surface for the alkaline etched substrate, while it is very limited for the degreased substrate. The surface potential (Volta potential) was investigated by scanning Kelvin probe force microscopy after different immersion times in CeCl 3 solution. The preferential deposition of Ce compounds at Al–Fe intermetallic sites progressively reduces their Volta potential difference relative to the matrix in the alkaline etched substrate. This reduces the susceptibility to localized attack of the intermetallics as proven by potentiodynamic polarization measurements

Uranium in alkaline rocks

Energy Technology Data Exchange (ETDEWEB)

Murphy, M.; Wollenberg, H.; Strisower, B.; Bowman, H.; Flexser, S.; Carmichael, I.

1978-04-01

Geologic and geochemical criteria were developed for the occurrence of economic uranium deposits in alkaline igneous rocks. A literature search, a limited chemical analytical program, and visits to three prominent alkaline-rock localities (Ilimaussaq, Greenland; Pocos de Caldas, Brazil; and Powderhorn, Colorado) were made to establish criteria to determine if a site had some uranium resource potential. From the literature, four alkaline-intrusive occurrences of differing character were identified as type-localities for uranium mineralization, and the important aspects of these localities were described. These characteristics were used to categorize and evaluate U.S. occurrences. The literature search disclosed 69 U.S. sites, encompassing nepheline syenite, alkaline granite, and carbonatite. It was possible to compare two-thirds of these sites to the type localities. A ranking system identified ten of the sites as most likely to have uranium resource potential.

Uranium in alkaline rocks

International Nuclear Information System (INIS)

Murphy, M.; Wollenberg, H.; Strisower, B.; Bowman, H.; Flexser, S.; Carmichael, I.

1978-04-01

Geologic and geochemical criteria were developed for the occurrence of economic uranium deposits in alkaline igneous rocks. A literature search, a limited chemical analytical program, and visits to three prominent alkaline-rock localities (Ilimaussaq, Greenland; Pocos de Caldas, Brazil; and Powderhorn, Colorado) were made to establish criteria to determine if a site had some uranium resource potential. From the literature, four alkaline-intrusive occurrences of differing character were identified as type-localities for uranium mineralization, and the important aspects of these localities were described. These characteristics were used to categorize and evaluate U.S. occurrences. The literature search disclosed 69 U.S. sites, encompassing nepheline syenite, alkaline granite, and carbonatite. It was possible to compare two-thirds of these sites to the type localities. A ranking system identified ten of the sites as most likely to have uranium resource potential

Alkaline pH sensor molecules.

Science.gov (United States)

Murayama, Takashi; Maruyama, Ichiro N

2015-11-01

Animals can survive only within a narrow pH range. This requires continual monitoring of environmental and body-fluid pH. Although a variety of acidic pH sensor molecules have been reported, alkaline pH sensor function is not well understood. This Review describes neuronal alkaline pH sensors, grouped according to whether they monitor extracellular or intracellular alkaline pH. Extracellular sensors include the receptor-type guanylyl cyclase, the insulin receptor-related receptor, ligand-gated Cl- channels, connexin hemichannels, two-pore-domain K+ channels, and transient receptor potential (TRP) channels. Intracellular sensors include TRP channels and gap junction channels. Identification of molecular mechanisms underlying alkaline pH sensing is crucial for understanding how animals respond to environmental alkaline pH and how body-fluid pH is maintained within a narrow range. © 2015 Wiley Periodicals, Inc.

Blood gas analysis, anion gap, and strong ion difference in horses treated with polyethylene glycol balanced solution (PEG 3350 or enteral and parenteral electrolyte solutions

Directory of Open Access Journals (Sweden)

Cláudio Luís Nina Gomes

2014-06-01

Full Text Available Large volumes of different electrolytes solutions are commonly used for ingesta hydration in horses with large colon impaction, but little is known about their consequences to blood acid-base balance. To evaluate the effects of PEG 3350 or enteral and parenteral electrolyte solutions on the blood gas analysis, anion gap and strong ion difference, five adult female horses were used in a 5x5 latin square design. The animals were divided in five groups and distributed to each of the following treatments: NaCl (0.9% sodium chloride solution; EES (enteral electrolyte solution, EES+LR (EES plus lactated Ringer's solution; PEG (balanced solution with PEG 3350 and PEG+LR (PEG plus lactated Ringer's solution. Treatments PEG or PEG + LR did not change or promoted minimal changes, while the EES caused a slight decrease in pH, but its association with lactated Ringer's solution induced increase in AG and SID values, as well as caused hypernatremia. In turn, the treatment NaCl generated metabolic acidosis. PEG 3350 did not alter the acid-base balance. Despite it's slight acidifying effect, the enteral electrolyte solution (EES did not cause clinically relevant changes.

The Alkaline Diet: Is There Evidence That an Alkaline ph Diet Benefits Health?

International Nuclear Information System (INIS)

Schwalfenberg, G.K.

2012-01-01

This review looks at the role of an alkaline diet in health. Pub med was searched looking for articles on ph, potential renal acid loads, bone health, muscle, growth hormone, back pain, vitamin D and chemotherapy. Many books written in the lay literature on the alkaline diet were also reviewed and evaluated in light of the published medical literature. There may be some value in considering an alkaline diet in reducing morbidity and mortality from chronic diseases and further studies are warranted in this area of medicine

Determination of trace amounts of chemical warfare agent degradation products in decontamination solutions with NMR spectroscopy.

Science.gov (United States)

Koskela, Harri; Rapinoja, Marja-Leena; Kuitunen, Marja-Leena; Vanninen, Paula

2007-12-01

Decontamination solutions are used for an efficient detoxification of chemical warfare agents (CWAs). As these solutions can be composed of strong alkaline chemicals with hydrolyzing and oxidizing properties, the analysis of CWA degradation products in trace levels from these solutions imposes a challenge for any analytical technique. Here, we present results of application of nuclear magnetic resonance spectroscopy for analysis of trace amounts of CWA degradation products in several untreated decontamination solutions. Degradation products of the nerve agents sarin, soman, and VX were selectively monitored with substantially reduced interference of background signals by 1D 1H-31P heteronuclear single quantum coherence (HSQC) spectrometry. The detection limit of the chemicals was at the low part-per-million level (2-10 microg/mL) in all studied solutions. In addition, the concentration of the degradation products was obtained with sufficient confidence with external standards.

Alkaline sodium borohydride gel as a hydrogen source for PEMFC or an energy carrier for NaBH{sub 4}-air battery

Energy Technology Data Exchange (ETDEWEB)

Liu, B.H. [Department of Materials and Engineering, Zhejiang University (China); Li, Z.P.; Chen, L.L. [Department of Chemical and Biochemical Engineering, Zhejiang University, Hangzhou 310027 (China)

2008-05-15

In this preliminary study, we tried to use sodium polyacrylate as the super absorbent polymer to form alkaline NaBH{sub 4} gel and explored its possibilities for borohydride hydrolysis and borohydride electro-oxidation. It was found that the absorption capacity of sodium polyacrylate decreased with increasing NaBH{sub 4} concentration. The formed gel was rather stable in the sealed vessel but tended to slowly decompose in open air. Hydrogen generation from the gel was carried out using CoCl{sub 2} catalyst precursor solutions. Hydrogen generation rate from the alkaline NaBH{sub 4} gel was found to be higher and impurities in hydrogen were less than that from the alkaline NaBH{sub 4} solution. The NaBH{sub 4} gel also successfully powered a NaBH{sub 4}-air battery. (author)

A study on alkaline heat treated Mg-Ca alloy for the control of the biocorrosion rate.

Science.gov (United States)

Gu, X N; Zheng, W; Cheng, Y; Zheng, Y F

2009-09-01

To reduce the biocorrosion rate by surface modification, Mg-Ca alloy (1.4wt.% Ca content) was soaked in three alkaline solutions (Na(2)HPO(4), Na(2)CO(3) and NaHCO(3)) for 24h, respectively, and subsequently heat treated at 773K for 12h. Scanning electron microscopy and energy-dispersive spectroscopy results revealed that magnesium oxide layers with the thickness of about 13, 9 and 26microm were formed on the surfaces of Mg-Ca alloy after the above different alkaline heat treatments. Atomic force microscopy showed that the surfaces of Mg-Ca alloy samples became rough after three alkaline heat treatments. The in vitro corrosion tests in simulated body fluid indicated that the corrosion rates of Mg-Ca alloy were effectively decreased after alkaline heat treatments, with the following sequence: NaHCO(3) heatedalkaline heat treated Mg-Ca alloy samples induced toxicity to L-929 cells during 7days culture.

Modifications of alkaline microgel electrophoresis for sensitive detection of DNA damage

International Nuclear Information System (INIS)

Singh, N.P.; Stephens, R.E.; Schneider, E.L.

1994-01-01

The alkaline microgel electrophoresis technique was modified to achieve a substantial increase in sensitivity for the detection of radiation-induced DNA damage in human lymphocytes. This increased sensitivity was achieved through: (1) the addition of free radical scavengers to the electrophoresis solution to reduce DNA damage generated during alkaline unwinding and electrophoresis; (2) the modification of the electrophoresis unit to achieve a more uniform electric field; (3) the use of YOYO-1, a DNA dye, producing fluorescence 500-fold more intense than ethidium bromide; and (4) the introduction of an image analysis system for the quantitation of DNA migration. In human lymphocytes, these modifications have resulted in an increased sensitivity of several fold, allowing the detection of DNA damage in the range of 50 mGy. (author)

Uranium mobility during interaction of rhyolitic obsidian, perlite and felsite with alkaline carbonate solution: T = 120° C, P = 210 kg/cm2

Science.gov (United States)

Zielinski, Robert A.

1979-01-01

Well-characterized samples of rhyolitic obsidian, perlite and felsite from a single lava flow are leached of U by alkaline oxidizing solutions under open-system conditions. Pressure, temperature, flow rate and solution composition are held constant in order to evaluate the relative importance of differences in surface area and crystallinity. Under the experimental conditions U removal from crushed glassy samples proceeds by a mechanism of glass dissolution in which U and silica are dissolved in approximately equal weight fractions. The rate of U removal from crushed glassy samples increases with decreasing average grain size (surface area). Initial rapid loss of a small component (≈ 2.5%) of the total U from crushed felsite. followed by much slower U loss, reflects variable rates of attack of numerous uranium sites. The fractions of U removed during the experiment ranged from 3.2% (felsite) to 27% (perlite). An empirical method for evaluating the relative rate of U loss from contemporaneous volcanic rocks is presented which incorporates leaching results and rock permeability data.

Blood gas analysis, anion gap, and strong ion difference in horses treated with polyethylene glycol balanced solution (PEG 3350) or enteral and parenteral electrolyte solutions

OpenAIRE

Gomes, Cláudio Luís Nina; Ribeiro Filho, José Dantas; Faleiros, Rafael Resende; Dantas, Fernanda Timbó D'el Rey; Amorim, Lincoln da Silva; Dantas, Waleska de Melo Ferreira

2014-01-01

Large volumes of different electrolytes solutions are commonly used for ingesta hydration in horses with large colon impaction, but little is known about their consequences to blood acid-base balance. To evaluate the effects of PEG 3350 or enteral and parenteral electrolyte solutions on the blood gas analysis, anion gap and strong ion difference, five adult female horses were used in a 5x5 latin square design. The animals were divided in five groups and distributed to each of the following tr...

Application of resin in pulp technique for ion exchange separation of uranium from alkaline leachate

International Nuclear Information System (INIS)

Sreenivas, T.; Rajan, K.; Chakravorty, J.

2014-01-01

The hydrometallurgical process for the recovery of uranium from different ores uses ion exchange (IX) technique for the separation of dissolved uranium values. Conventionally, the IX process is carried out on leach solution obtained after the filtration or counter-current decantation of the leach slurries. Amongst the two types of leach pulps generated in uranium ore processing, viz acidic and alkaline, the latter one consists of predominantly fine-size pulps of higher viscosity, thus making the solid-liquid separation an arduous task. Sustained research for improvising the efficiency of various unit operations in the uranium process flowsheet have resulted in advent of new generation resins which are mechanically re-silent, posses higher exchange capacity thereby enabling separation of dissolved uranium ions from the leach pulps directly. Some of the prominent low-grade uranium ore deposits in India are hosted in acid consuming gangue matrix. These ore deposits necessitate fine grinding as well as application of alkaline leaching for the dissolution of uranium values. The leach pulps analyse 500 – 600 mg/l of U3O8 and contain total dissolved solutes (TDS) to the extent of about 50 g/l. Analysis of the characteristics of the leach pulp indicated suitability of resin-in-pulp technique for the separation of uranyl carbonate anions from the leachate. This paper describes the results of the RIP test work on alkaline leach slurry using various commercially available strong base anionic exchange resins. Parametric variation studies were conducted to establish the adsorption isotherm and sorption kinetics followed by elution of loaded uranium. Based on these results semi-continuous experiments on “carousel” mode were carried out. The results indicate superiority of gel type polystyrene based resins grafted with quaternary ammonium ion in comparison to the macro-porous resins. Semi-continuous counter-current extraction and elution tests indicated that about 98% of

Alkaline treatment on piassava (Attalea funifera martius) fiber

International Nuclear Information System (INIS)

Santos, E.B.C.; Moreno, C.G.; Barros, J.J.P.; Moura, D.A.; Fim, F.C.; Wellen, R.M.R.; Silva, L.B.

2016-01-01

Alkaline treatment on piassava fiber with size inferior to 270 mesh was performed to remove impurities. The treatments took place under magnetic stirring and Sodium Hydroxide (NaOH) solution with 2, 4, 6 and 8% of concentration; processing time ranged between 100 and 400 minutes, with intervals of 25 minutes; the main object was to reach the optimum concentration and time. The concentration 2% was used to remove efficiently the impurities without damaging excessively the fiber. The fibers were characterized by means of X-ray diffraction (XRD) and optical microscopy (OM). Fibers presented XRD diffraction peak around 22 deg, due to the crystalline structure of cellulose. By optical microscopy was observed the treatment efficacy of the 2% NaOH solution in removing surface impurities. (author)

Trial of an experimental castor oil solution for cleaning dentures.

Science.gov (United States)

Andrade, Ingrid Machado de; Andrade, Kelly Machado de; Pisani, Marina Xavier; Silva-Lovato, Cláudia Helena; de Souza, Raphael Freitas; Paranhos, Helena de Freitas Oliveira

2014-01-01

Denture hygiene is essential because denture biofilm is involved in oral infections and systemic diseases. Although there are chemical agents available on the market, none of them have ideal properties and research on such products is still necessary. The aim of this study was to evaluate the efficacy of a castor bean (Ricinus communis)-based solution for removing denture biofilm, compared to two traditional products (sodium hypochlorite and alkaline peroxide). Fifty maxillary complete denture wearers were instructed to brush their dentures after meals and to immerse their dentures once a day in the following solutions: Saline (20 min; control), Polident alkaline peroxide (3 min), NaOCl (20 min) and 2% castor oil solution (20 min). Participants used each solution for a period of 7 consecutive days, according to a random sequence. After each period, the internal surfaces of maxillary complete dentures were stained with a disclosing solution (1% neutral red), photographed and the disclosed biofilm was quantified with the aid of specific software. The influence of treatments on results was verified by the Friedman test (α=0.05). Tested solutions presented significant difference (Fr=51.67; pcastor oil presented intermediate results (median: 1.0% and 1.5%, respectively). It can be concluded that the castor oil solution tested in this study was comparable to alkaline peroxide in terms of efficiency in denture biofilm removal.

Self-similar solutions for implosion and reflection of strong and weak shocks in a plasma

International Nuclear Information System (INIS)

Desai, B.N.; Chavda, L.K.

1980-06-01

We present an improved approximation scheme for finding approximate solutions in analytic form to the self-similar equations of gas dynamics. The method gives better agreement with exact results not only for the weak shocks which were considered previously but also for strong shocks for which the previous method gave poor results. We have considered various shock configurations in spherical and cylindrical geometries. (author)

Relative entropies, suitable weak solutions, and weak-strong uniqueness for the compressible Navier–Stokes system

Czech Academy of Sciences Publication Activity Database

Feireisl, Eduard; Jin, B.J.; Novotný, A.

2012-01-01

Roč. 14, č. 4 (2012), s. 717-730 ISSN 1422-6928 R&D Projects: GA ČR GA201/09/0917 Institutional research plan: CEZ:AV0Z10190503 Keywords : suitable weak solution * weak-strong uniqueness * compressible Navier-Stokes system Subject RIV: BA - General Mathematics Impact factor: 1.415, year: 2012 http://link.springer.com/article/10.1007%2Fs00021-011-0091-9

Enzymatic Hydrolysis of Alkaline Pretreated Coconut Coir

Directory of Open Access Journals (Sweden)

Akbarningrum Fatmawati

2013-06-01

Full Text Available The purpose of this research is to study the effect of concentration and temperature on the cellulose and lignin content, and the reducing sugars produced in the enzymatic hydrolysis of coconut coir. In this research, the coconut coir is pretreated using 3%, 7%, and 11% NaOH solution at 60oC, 80oC, and 100oC. The pretreated coir were assayed by measuring the amount of cellulose and lignin and then hydrolysed using Celluclast and Novozyme 188 under various temperature (30oC, 40oC, 50oC and pH (3, 4, 5. The hydrolysis results were assayed for the reducing sugar content. The results showed that the alkaline delignification was effective to reduce lignin and to increase the cellulose content of the coir. The best delignification condition was observed at 11% NaOH solution and 100oC which removed 14,53% of lignin and increased the cellulose content up to 50,23%. The best condition of the enzymatic hydrolysis was obtained at 50oC and pH 4 which produced 7,57 gr/L reducing sugar. © 2013 BCREC UNDIP. All rights reservedReceived: 2nd October 2012; Revised: 31st January 2013; Accepted: 6th February 2013[How to Cite: Fatmawati, A., Agustriyanto, R., Liasari, Y. (2013. Enzymatic Hydrolysis of Alkaline Pre-treated Coconut Coir. Bulletin of Chemical Reaction Engineering & Catalysis, 8 (1: 34-39 (doi:10.9767/bcrec.8.1.4048.34-39[Permalink/DOI: http://dx.doi.org/10.9767/bcrec.8.1.4048.34-39] | View in  |

Conceptual Model of Uranium in the Vadose Zone for Acidic and Alkaline Wastes Discharged at the Hanford Site Central Plateau

Energy Technology Data Exchange (ETDEWEB)

Truex, Michael J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Szecsody, James E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Qafoku, Nikolla [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Serne, R. Jeffrey [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2014-09-01

Historically, uranium was disposed in waste solutions of varying waste chemistry at the Hanford Site Central Plateau. The character of how uranium was distributed in the vadose zone during disposal, how it has continued to migrate through the vadose zone, and the magnitude of potential impacts on groundwater are strongly influenced by geochemical reactions in the vadose zone. These geochemical reactions can be significantly influenced by the disposed-waste chemistry near the disposal location. This report provides conceptual models and supporting information to describe uranium fate and transport in the vadose zone for both acidic and alkaline wastes discharged at a substantial number of waste sites in the Hanford Site Central Plateau. The conceptual models include consideration of how co-disposed acidic or alkaline fluids influence uranium mobility in terms of induced dissolution/precipitation reactions and changes in uranium sorption with a focus on the conditions near the disposal site. This information, when combined with the extensive information describing uranium fate and transport at near background pH conditions, enables focused characterization to support effective fate and transport estimates for uranium in the subsurface.

Structural Features of Alkaline Extracted Polysaccharide from the Seeds of Plantago asiatica L. and Its Rheological Properties

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Jun-Yi Yin

2016-09-01

Full Text Available Polysaccharide from the seeds of Plantago asiatica L. has many bioactivities, but few papers report on the structural and rheological characteristics of the alkaline extract. The alkaline extracted polysaccharide was prepared from seeds of P. asiatica L. and named herein as alkaline extracted polysaccharide from seeds of P. asiatica L. (PLAP. Its structural and rheological properties were characterized by monosaccharide composition, methylation, GC-MS and rheometry. PLAP, as an acidic arabinoxylan, was mainly composed of 1,2,4-linked Xylp and 1,3,4-linked Xylp residues. PLAP solution showed pseudoplastic behavior, and weak gelling properties at high concentration. Sodium and especially calcium ions played a significant role in increasing the apparent viscosity and gel strength.

Titanium Nitride Nanoparticle Electrocatalysts for Oxygen Reduction Reaction in Alkaline Solution

KAUST Repository

Ohnishi, R.

2013-03-12

Monodispersed TiN nanoparticles with a narrow size distribution (7–23 nm) were synthesized using mesoporous graphitic (mpg)-C3N4 templates with different pore sizes. The nano-materials were examined as electrocatalysts for oxygen reduction reaction (ORR) in alkaline media. The TiN nanoparticles were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), N2 sorption, transmission electron microscopy (TEM), and C-H-N elemental analysis. The ORR current increased as the TiN particle size decreased, and hence the surface area of TiN nanoparticles reactive to ORR increased. Rotating ring disk electrode (RRDE) measurements revealed that the ORR on TiN surfaces proceeded mainly via a two-electron pathway, producing H2O2 as the main product. Mechanistic aspects of ORR on TiN surfaces are discussed.

Titanium Nitride Nanoparticle Electrocatalysts for Oxygen Reduction Reaction in Alkaline Solution

KAUST Repository

Ohnishi, R.; Katayama, M.; Cha, Dong Kyu; Takanabe, Kazuhiro; Kubota, J.; Domen, K.

2013-01-01

Monodispersed TiN nanoparticles with a narrow size distribution (7–23 nm) were synthesized using mesoporous graphitic (mpg)-C3N4 templates with different pore sizes. The nano-materials were examined as electrocatalysts for oxygen reduction reaction (ORR) in alkaline media. The TiN nanoparticles were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), N2 sorption, transmission electron microscopy (TEM), and C-H-N elemental analysis. The ORR current increased as the TiN particle size decreased, and hence the surface area of TiN nanoparticles reactive to ORR increased. Rotating ring disk electrode (RRDE) measurements revealed that the ORR on TiN surfaces proceeded mainly via a two-electron pathway, producing H2O2 as the main product. Mechanistic aspects of ORR on TiN surfaces are discussed.

Strong solutions for the Navier-Stokes equations on bounded and unbounded domains with a moving boundary

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Juergen Saal

2007-02-01

Full Text Available It is proved under mild regularity assumptions on the data that the Navier-Stokes equations in bounded and unbounded noncylindrical regions admit a unique local-in-time strong solution. The result is based on maximal regularity estimates for the in spatial regions with a moving boundary obtained in [16] and the contraction mapping principle.

Alkalinity of the Mediterranean Sea

OpenAIRE

Schneider, Anke; Wallace, Douglas W.R.; Körtzinger, Arne

2007-01-01

Total alkalinity (AT) was measured during the Meteor 51/2 cruise, crossing the Mediterranean Sea from west to east. AT concentrations were high (∼2600 μmol kg−1) and alkalinity-salinity-correlations had negative intercepts. These results are explained by evaporation coupled with high freshwater AT inputs into coastal areas. Salinity adjustment of AT revealed excess alkalinity throughout the water column compared to mid-basin surface waters. Since Mediterranean waters are supersaturated with r...

Tooth enamel sample preparation using alkaline treatment in ESR dosimetry

International Nuclear Information System (INIS)

Yongzeng, Zhou; Jiadong, Wang; Xiaomei, Jia; Ke, Wu; Jianbo, Cong

2002-01-01

Tooth enamel sample preparation using alkaline treatment was studied and compared with traditional mechanical method in this paper. 20 adult teeth were used. Samples were placed into NaOH solution. This method requires 4-5 weeks and the enamel was separated from dentin. Experimental results show that 8M NaOH was appropriate for separating enamel from dentin and that there is no difference in background signal relative intensity between samples prepared by mechanical and by chemical methods. There is also no difference in radiosensitivity between samples prepared by two methods mentioned above. Dose response curve for tooth enamel samples isolated by 8M NaOH solution was obtained

Strong convergence and convergence rates of approximating solutions for algebraic Riccati equations in Hilbert spaces

Science.gov (United States)

Ito, Kazufumi

1987-01-01

The linear quadratic optimal control problem on infinite time interval for linear time-invariant systems defined on Hilbert spaces is considered. The optimal control is given by a feedback form in terms of solution pi to the associated algebraic Riccati equation (ARE). A Ritz type approximation is used to obtain a sequence pi sup N of finite dimensional approximations of the solution to ARE. A sufficient condition that shows pi sup N converges strongly to pi is obtained. Under this condition, a formula is derived which can be used to obtain a rate of convergence of pi sup N to pi. The results of the Galerkin approximation is demonstrated and applied for parabolic systems and the averaging approximation for hereditary differential systems.

Extraction of Zinc and Manganese from Alkaline and Zinc-Carbon Spent Batteries by Citric-Sulphuric Acid Solution

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Francesco Ferella

2010-01-01

Full Text Available The paper is focused on the recovery of zinc and manganese from alkaline and zinc-carbon spent batteries. Metals are extracted by sulphuric acid leaching in the presence of citric acid as reducing agent. Leaching tests are carried out according to a 24 full factorial design, and empirical equations for Mn and Zn extraction yields are determined from experimental data as a function of pulp density, sulphuric acid concentration, temperature, and citric acid concentration. The highest values experimentally observed for extraction yields were 97% of manganese and 100% of zinc, under the following operating conditions: temperature 40∘C, pulp density 20%, sulphuric acid concentration 1.8 M, and citric acid 40 g L-1. A second series of leaching tests is also performed to derive other empirical models to predict zinc and manganese extraction. Precipitation tests, aimed both at investigating precipitation of zinc during leaching and at evaluating recovery options of zinc and manganese, show that a quantitative precipitation of zinc can be reached but a coprecipitation of nearly 30% of manganese also takes place. The achieved results allow to propose a battery recycling process based on a countercurrent reducing leaching by citric acid in sulphuric solution.

In situ surface X-ray diffraction study of ultrathin epitaxial Co films on Au(111) in alkaline solution

International Nuclear Information System (INIS)

Reikowski, Finn; Maroun, Fouad; Di, Nan; Allongue, Philippe; Ruge, Martin; Stettner, Jochim; Magnussen, Olaf M.

2016-01-01

The oxidation behavior of ultrathin electrodeposited Co films on Au(111) in alkaline electrolyte was studied using in situ surface X-ray scattering techniques employing synchrotron radiation and complementary optical reflectivity and electrochemical measurements. The films are formed at pH 4 and consist of (001)-oriented hcp Co crystallites that are several nm high, a few ten nm in diameter, and remain largely unchanged after electrolyte exchange to pH 12 solution. In the pre-oxidation peak only minor changes were observed in the diffraction studies, excluding the formation of Co(OH)_2 layers. In the potential regime of Co hydroxide formation a rapid reduction of the amount of Co is observed, while the characteristic height of the islands decreases only slightly. On longer times scales, growth of 3D crystals of Co(OH)_2 occurs as well as irreversible Co dissolution into the electrolyte is found. On the basis of the structural observations oxidation of the Co film is proposed to proceed via fast formation of an ultrathin passivating layer, followed by nucleation and growth of 3D hydroxide crystals at the grain boundaries in the Co deposit.

Transpassive electrodissolution of depleted uranium in alkaline electrolytes

International Nuclear Information System (INIS)

Weisbrod, K.R.; Schake, A.R.; Morgan, A.N.; Purdy, G.M.; Martinez, H.E.; Nelson, T.O.

1998-03-01

To aid in removal of oralloy from the nuclear weapons stockpile, scientists at the Los Alamos National Laboratory Plutonium Facility are decontaminating oralloy parts by electrodissolution in neutral to alkaline electrolytes composed of sodium nitrate and sodium sulfate. To improve the process, electrodissolution experiments were performed with depleted uranium to understand the effects of various operating parameters. Sufficient precipitate was also produced to evaluate the feasibility of using ultrafiltration to separate the uranium oxide precipitates from the electrolyte before it enters the decontamination fixture. In preparation for the experiments, a potential-pH diagram for uranium was constructed from thermodynamic data for fully hydrated species. Electrodissolution in unstirred solutions showed that uranium dissolution forms two layers, an acidic bottom layer rich in uranium and an alkaline upper layer. Under stirred conditions results are consistent with the formation of a yellow precipitate of composition UO 3 ·2H 2 O, a six electron process. Amperometric experiments showed that current efficiency remained near 100% over a wide range of electrolytes, electrolyte concentrations, pH, and stirring conditions

Effect of alkaline addition on anaerobic sludge digestion with combined pretreatment of alkaline and high pressure homogenization.

Science.gov (United States)

Fang, Wei; Zhang, Panyue; Zhang, Guangming; Jin, Shuguang; Li, Dongyi; Zhang, Meixia; Xu, Xiangzhe

2014-09-01

To improve anaerobic digestion efficiency, combination pretreatment of alkaline and high pressure homogenization was applied to pretreat sewage sludge. Effect of alkaline dosage on anaerobic sludge digestion was investigated in detail. SCOD of sludge supernatant significantly increased with the alkaline dosage increase after the combined pretreatment because of sludge disintegration. Organics were significantly degraded after the anaerobic digestion, and the maximal SCOD, TCOD and VS removal was 73.5%, 61.3% and 43.5%, respectively. Cumulative biogas production, methane content in biogas and biogas production rate obviously increased with the alkaline dosage increase. Considering both the biogas production and alkaline dosage, the optimal alkaline dosage was selected as 0.04 mol/L. Relationships between biogas production and sludge disintegration showed that the accumulative biogas was mainly enhanced by the sludge disintegration. The methane yield linearly increased with the DDCOD increase as Methane yield (ml/gVS)=4.66 DDCOD-9.69. Copyright © 2014 Elsevier Ltd. All rights reserved.

Correlation of Surface Adsorption and Oxidation with a Floatability Difference of Galena and Pyrite in High-Alkaline Lime Systems.

Science.gov (United States)

Niu, Xiaopeng; Ruan, Renman; Xia, Liuyin; Li, Li; Sun, Heyun; Jia, Yan; Tan, Qiaoyi

2018-02-27

When it comes to Pb-Zn ores with high amounts of pyrite, the major problem encountered is the low separation efficiency between galena and pyrite. By virtue of high dosage of lime and collector sodium diethyl dithiocarbamate (DDTC), pyrite and zinc minerals are depressed, allowing the galena to be floated. However, there have been significant conflicting reports on the flotation behavior of galena at high pH. In this context, correlation of the surface adsorption and oxidation with the floatability difference of galena and pyrite in high-alkaline lime systems would be a key issue for process optimization. Captive bubble contact angle measurements were performed on freshly polished mineral surfaces in situ exposed to lime solutions of varying pH as a function of immersion time. Furthermore, single mineral microflotation tests were conducted. Both tests indicated that the degree of hydrophobicity on the surfaces of galena and pyrite increased in the presence of DDTC at natural or mild pulp pH. While in a saturated lime solution, at pH 12.5, DDTC only worked for galena, but not for pyrite. Surface chemistry analysis by time-of-flight secondary ion mass spectrometry (Tof-SIMS) confirmed the preference of DDTC on the galena surface at pH 12.5, which contributed to a merit recovery. Further important evidence through measurements of Tof-SIMS, ion chromatography, and high-performance liquid chromatography indicated that in high-alkaline lime systems, the merit floatability of galena could exclude the insignificant contribution of elemental sulfur (S 8 ) and was dominantly attributed by the strong adsorption of DDTC. In contrast, the poor flotation response of pyrite at high pH was due to the prevailing adsorption of CaOH + species. This study provides an important surface chemistry evidence for a better understanding of the mechanism on the better selectivity in the galena-pyrite separation adopting high-alkaline lime systems.

The Alkaline Diet: Is There Evidence That an Alkaline pH Diet Benefits Health?

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Gerry K. Schwalfenberg

2012-01-01

Full Text Available This review looks at the role of an alkaline diet in health. Pubmed was searched looking for articles on pH, potential renal acid loads, bone health, muscle, growth hormone, back pain, vitamin D and chemotherapy. Many books written in the lay literature on the alkaline diet were also reviewed and evaluated in light of the published medical literature. There may be some value in considering an alkaline diet in reducing morbidity and mortality from chronic diseases and further studies are warranted in this area of medicine.

Stainless steel anodes for alkaline water electrolysis and methods of making

Science.gov (United States)

Soloveichik, Grigorii Lev

2014-01-21

The corrosion resistance of stainless steel anodes for use in alkaline water electrolysis was increased by immersion of the stainless steel anode into a caustic solution prior to electrolysis. Also disclosed herein are electrolyzers employing the so-treated stainless steel anodes. The pre-treatment process provides a stainless steel anode that has a higher corrosion resistance than an untreated stainless steel anode of the same composition.

Pseudomonas syringae evades host immunity by degrading flagellin monomers with alkaline protease AprA

NARCIS (Netherlands)

Pel, Michiel J C; van Dijken, Anja J H; Bardoel, Bart W; Seidl, Michael F; van der Ent, Sjoerd; van Strijp, Jos A G; Pieterse, Corné M J

Bacterial flagellin molecules are strong inducers of innate immune responses in both mammals and plants. The opportunistic pathogen Pseudomonas aeruginosa secretes an alkaline protease called AprA that degrades flagellin monomers. Here, we show that AprA is widespread among a wide variety of

Pseudomonas syringae evades host Immunity by degrading flagellin monomers with alkaline protease AprA

NARCIS (Netherlands)

Pel, M.J.C.; Van Dijken, A.J.H.; Bardoel, B.W.; Seidl, M.F; Van der Ent, S.; Van Strijp, J.A.G.

2014-01-01

Bacterial flagellin molecules are strong inducers of innate immune responses in both mammals and plants. The opportunistic pathogen Pseudomonas aeruginosa secretes an alkaline protease called AprA that degrades flagellin monomers. Here, we show that AprA is widespread among a wide variety of

Novel Extraction Process Of Rare Earth Elements From NdFeB Powders Via Alkaline Treatment

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Chung K.W.

2015-06-01

Full Text Available The alkaline treatment of NdFeB powders in NaOH solution at various equivalent amounts of NaOH at 100°C was performed. The resultant powders were then leached in 0.5M H2SO4 solution at 25°C for 2 minutes. At 5 equivalents of NaOH, neodymium in NdFeB powders was partially transformed to neodymium hydroxide. The transformation of neodymium to neodymium hydroxide actually occurred at 10 equivalents of NaOH and was facilitated by increasing the equivalent of NaOH from 10 to 30. In addition, iron was partially transformed to magnetite during the alkaline treatment, which was also promoted at a higher equivalent of NaOH. The leaching yield of neodymium from alkaline-treated powders was increased with an increasing equivalent of NaOH up to 10; however, it slightly decreased with the equivalent NaOH of over 10. The leaching yield of iron was inversely proportional to that of rare earth elements. NdFeB powders treated at 10 equivalents of NaOH showed a maximum leaching yield of neodymium and dysprosium of 91.6% and 94.6%, respectively, and the lowest leaching yield of iron of 24.2%, resulting in the highest selective leaching efficiency of 69.4%.

On the strong solution of a class of partial differential equations that arise in the pricing of mortgage backed securities

KAUST Repository

Parshad, Rana; Bayazit, Derviş; Barlow, Nathaniel S.; Prasad, V. Ramchandra

2011-01-01

We consider a reduced form pricing model for mortgage backed securities, formulated as a non-linear partial differential equation. We prove that the model possesses a weak solution. We then show that under additional regularity assumptions on the initial data, we also have a mild solution. This mild solution is shown to be a strong solution via further regularity arguments. We also numerically solve the reduced model via a Fourier spectral method. Lastly, we compare our numerical solution to real market data. We observe interestingly that the reduced model captures a number of recent market trends in this data, that have escaped previous models.

Removal of tartrazine from aqueous solutions by strongly basic polystyrene anion exchange resins.

Science.gov (United States)

Wawrzkiewicz, Monika; Hubicki, Zbigniew

2009-05-30

The removal of tartrazine from aqueous solutions onto the strongly basic polystyrene anion exchangers of type 1 (Amberlite IRA-900) and type 2 (Amberlite IRA-910) was investigated. The experimental data obtained at 100, 200, 300 and 500 mg/dm(3) initial concentrations at 20 degrees C were applied to the pseudo-first order, pseudo-second order and Weber-Morris kinetic models. The calculated sorption capacities (q(e,cal)) and the rate constant of the first order adsorption (k(1)) were determined. The pseudo-second order kinetic constants (k(2)) and capacities were calculated from the plots of t/q(t) vs. t, 1/q(t) vs. 1/t, 1/t vs. 1/q(t) and q(t)/t vs. q(t) for type 1, type 2, type 3 and type 4 of the pseudo-second order expression, respectively. The influence of phase contact time, solution pH and temperature on tartrazine removal was also discussed. The FTIR spectra of pure anion exchangers and those loaded with tartrazine were recorded, too.

Determination of Acidity and Alkalinity of Food Materials

OpenAIRE

三浦,芳助; 福永,祐子; 瀧川,裕里子; 津田,真美; 渡辺,陽子; 瀨山,一正

2006-01-01

The acidity and alkalinity of food materials in various menus was determined to clarify the influence of food on physiological functions.　Menus mainly containing alkaline food materials (alkaline menu) and acid ones (acid menu) were compared.　Determination of acidity and alkalinity was performed for each food material in the alkaline menu and acid menu, and acidity and alkalinity of one meal and a day's one were estimated. １.　Most of food materials in acid menu were assessed to be...

Development of conductometric biosensors based on alkaline phosphatases for the water quality control

Science.gov (United States)

Berezhetskyy, A.

2008-09-01

Researches are focused on the elaboration of enzymatic microconductometric device for heavy metal ions detection in water solutions. The manuscript includes a general introduction, the first chapter contains bibliographic review, the second chapter described the fundamentals of conductometric transducers, the third chapter examining the possibility to create and to optimize conductometric biosensor based on bovine alkaline phosphatase for heavy metals ions detection, the fourth chapter devoted to creation and optimization of conductometric biosensor based on alkaline phosphatase active microalgae and sol gel technology, the last chapter described application of the proposed algal biosensor for measurements of heavy metal ions toxicity of waste water, general conclusions stating the progresses achieved in the field of environmental monitoring

Numerical path integral solution to strong Coulomb correlation in one dimensional Hooke's atom

Science.gov (United States)

Ruokosenmäki, Ilkka; Gholizade, Hossein; Kylänpää, Ilkka; Rantala, Tapio T.

2017-01-01

We present a new approach based on real time domain Feynman path integrals (RTPI) for electronic structure calculations and quantum dynamics, which includes correlations between particles exactly but within the numerical accuracy. We demonstrate that incoherent propagation by keeping the wave function real is a novel method for finding and simulation of the ground state, similar to Diffusion Monte Carlo (DMC) method, but introducing new useful tools lacking in DMC. We use 1D Hooke's atom, a two-electron system with very strong correlation, as our test case, which we solve with incoherent RTPI (iRTPI) and compare against DMC. This system provides an excellent test case due to exact solutions for some confinements and because in 1D the Coulomb singularity is stronger than in two or three dimensional space. The use of Monte Carlo grid is shown to be efficient for which we determine useful numerical parameters. Furthermore, we discuss another novel approach achieved by combining the strengths of iRTPI and DMC. We also show usefulness of the perturbation theory for analytical approximates in case of strong confinements.

Changes in hydraulic conductivity of sand-bentonite mixtures accompanied with alkaline alteration

International Nuclear Information System (INIS)

Yamaguchi, Tetsuji; Sawaguchi, Takuma; Tsukada, Manabu; Tanaka, Tadao

2012-01-01

Document available in extended abstract form only. Montmorillonite is the main constituent of bentonite clay buffer materials in radioactive waste repositories. Highly alkaline environments induced by cement based materials are likely to alter montmorillonite, and to deteriorate the physical and/or chemical properties of the buffer materials. The deterioration may cause variation in hydraulic conductivity of the buffer and induce major uncertainties in the radionuclide migration analysis. Empirical data on the variation of hydraulic conductivity are, however, scarce mainly because the alteration of compacted buffer materials, sand-bentonite mixture specimen, is extremely slow (1). In this study, laboratory experiments were performed to observe changes in hydraulic conductivity of sand-bentonite mixtures accompanied with their alkaline alteration using NaOH based solutions at 80 - 90 deg. C. Our preliminary attempt to degrade sand-bentonite mixture by permeating alkaline solutions was unsuccessful, in which the flow rate of water became unstable. This was interpreted as an artifact due to generation and stagnation of air in the mixture specimen. The water conduction experimental apparatus was modified by removing membrane filter and leaving only sintered stainless steel filter, and by equipping the pressurizing tank with a preheater. Three types of experiments were performed afterwards. Series-1: Multi step alteration / water-conduction experiments. Two sand-bentonite mixture specimens with 50 mm in diameter, 10 mm in thickness and 1,600 kg m -3 in dry density were applied to hydraulic conductivity measurement and alkaline alteration process alternately. The mixture ratio was 1:1 in dry weight. The hydraulic conductivity was determined by permeating the specimens with 1.0 mol L -1 NaCl solution at 40 deg. C. While the specimens were immersed in Si, Al and Ca-adjusted 1.0 mol L -1 NaOH solution at 90 deg. C to allow alteration. In the final water-conduction step, the

Alkaline Peroxides Versus Sodium Hypochlorite for Removing Denture Biofilm: a Crossover Randomized Trial.

Science.gov (United States)

Peracini, Amanda; Regis, Rômulo Rocha; Souza, Raphael Freitas de; Pagnano, Valéria Oliveira; Silva, Cláudia Helena Lovato da; Paranhos, Helena de Freitas Oliveira

2016-01-01

This study evaluated the efficacy of cleanser solutions on denture biofilm removal by a crossover randomized clinical trial. Thirty two edentulous patients were instructed to brush their dentures (specific brush and liquid soap) three times a day (after breakfast, lunch and dinner) and to soak them (≥ 8 h) in: (C) control -water; (AP): alkaline peroxide; or (SH) 0.5% sodium hypochlorite. Each solution was used for 21 days (three cycles of 7 days). At the end of each cycle, the inner surfaces of maxillary dentures were disclosed (1% neutral red) and photographed (HX1 - Sony). Areas (total and stained biofilm) were measured (Image Tool software) and the percentage of biofilm calculated as the ratio between the area of the biofilm multiplied by 100 and total surface area of the internal base of the denture. Data were compared by means of generalized estimating equation (α=5%) and multiple comparisons (Bonferroni; α=1.67%). Immersion in SH reduced biofilm (%) (8.3 ± 13.3B) compared to C (18.2 ± 14.9A) and AP (18.2 ± 16.6A). The 0.5% sodium hypochlorite solution was the most efficacious for biofilm removal. Alkaline peroxides may not lead to further biofilm removal in patients with adequate denture maintenance habits.

Growth and Tissue Elemental Composition Response of Butterhead Lettuce (Lactuca sativa, cv. Flandria to Hydroponic Conditions at Different pH and Alkalinity

Directory of Open Access Journals (Sweden)

Tyler S. Anderson

2017-07-01

Full Text Available Biomass and tissue elemental differences were quantified for lettuce grown in deep-water conventional hydroponic conditions at two pH and alkalinity conditions. Nutrient solutions were created using inorganic salts and either reverse osmosis (RO water or municipal water with high alkalinity. Three treatments were evaluated: (a nutrient solution created with reverse osmosis (RO water and maintained at pH 5.8 (H5; (b same as H5 but maintained at pH 7.0 (H7; and (c nutrient solution created using municipal water and maintained at pH 7.0, referred to as HA7. Averaged across three trials, the HA7 and H7 treatments produced 26% less shoot fresh weight (FW than the H5 treatment with an 18% reduction in dry weight (DW. The H5 treatment had the least biomass in root FW and DW. In tissue elemental analyses, both the pH 7.0 treatments showed lower concentrations than H5 in Cu, N, Mo, and Sr, and increased concentrations in Ba, Mg, Na, and Zn. There were no differences in Al, C, Ca, Fe, K, Mn, Ni, P, S, and Si concentrations among treatments (p = 0.05. The results from this experiment can be used to isolate the effects of pH and alkalinity in aquaponic conditions where pH and alkalinity will mimic HA7 conditions.

Anodic oxidation of ammonia in alkaline solutions at Pt/Pt electrodes. Hakkin denkyokujo ni okeru enkisei ammonia yoeki no anodo sanka

Energy Technology Data Exchange (ETDEWEB)

Takagi, Ryoichiro; Katsuta, Masahiro; Matsumoto, Tamotsu; Kobayashi, Yoshikazu; Asami, Yusaku; Hirano, Katsuhiko (Shibaura Inst. of Tech., Tokyo (Japan))

1989-01-05

Anodic oxidation of ammonia in alkaline solutions on Pt/Pt electrode, in which NH {sub 3} is oxidized producing N {sub 2}, is a promising reaction in application to a fuel cell and water treatment. In this study, the relations between electrode potential and adsorbed intermediates, reaction process were elucidated by potentiodynamic method and potential step method. In measurement, a transient memory device and a microprocessor were connected to an electrolysis device as a new method, then measurement of electric potential and current and integral calculation were perfromed at high speed. Active sites of electrode were covered by Pt NH {sub x}. Faradic current corresponds to the N {sub 2} evolution was shown markedly by anodic scanning. The relation between electrode potential and reaction process was revealed by potential step method. It is found that Pt-NH {sub 2} is the active intermediate for the N {sub 2} evolution, and when current shows maximum, its coverage is nearly 0.5. 15 refs., 7 figs.

Interannual sedimentary effluxes of alkalinity in the southern North Sea: model results compared with summer observations

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J. Pätsch

2018-06-01

Full Text Available For the sediments of the central and southern North Sea different sources of alkalinity generation are quantified by a regional modelling system for the period 2000–2014. For this purpose a formerly global ocean sediment model coupled with a pelagic ecosystem model is adapted to shelf sea dynamics, where much larger turnover rates than in the open and deep ocean occur. To track alkalinity changes due to different nitrogen-related processes, the open ocean sediment model was extended by the state variables particulate organic nitrogen (PON and ammonium. Directly measured alkalinity fluxes and those derived from Ra isotope flux observation from the sediment into the pelagic are reproduced by the model system, but calcite building and calcite dissolution are underestimated. Both fluxes cancel out in terms of alkalinity generation and consumption. Other simulated processes altering alkalinity in the sediment, like net sulfate reduction, denitrification, nitrification, and aerobic degradation, are quantified and compare well with corresponding fluxes derived from observations. Most of these fluxes exhibit a strong positive gradient from the open North Sea to the coast, where large rivers drain nutrients and organic matter. Atmospheric nitrogen deposition also shows a positive gradient from the open sea towards land and supports alkalinity generation in the sediments. An additional source of spatial variability is introduced by the use of a 3-D heterogenous porosity field. Due to realistic porosity variations (0.3–0.5 the alkalinity fluxes vary by about 4 %. The strongest impact on interannual variations of alkalinity fluxes is exhibited by the temporal varying nitrogen inputs from large rivers directly governing the nitrate concentrations in the coastal bottom water, thus providing nitrate necessary for benthic denitrification. Over the time investigated the alkalinity effluxes decrease due to the decrease in the nitrogen supply by the rivers.

Precipitation of uranium oxide by reduction in alkaline solution; Precipitation d'oxyde d'uranium par reduction en milieu alcalin

Energy Technology Data Exchange (ETDEWEB)

Pottier, P; Claus, J [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

1964-07-01

In the first part of the report the authors study the reaction mechanism for this reduction which makes it possible to precipitate a hydrated uranium oxide from alkaline uranyl carbonate solutions. The research into the effects of different variables on numerous cycles are then summarized. Optical, X-ray and thermogravimetric examinations then make it possible to predict the properties of this oxide. In the second part the authors carry out calculations for the continuous operation of single cells and cells in series. These calculations give the data required for the construction of 2 cells having capacities of 0.3 and 10 litres. Results obtained from the continuous operation of this latter cell lead to certain conclusions concerning the applicability of this method to the hydrometallurgy of uranium. (authors) [French] Dans une premiere partie, les auteurs etudient le mecanisme de reaction de cette reduction qui permet la precipitation d'un oxyde d'uranium hydrate dans les solutions d'uranyle-carbonates alcalins. Les etudes de diverses variables sur de nombreux cycles sont ensuite resumees. Puis des examens optiques, aux rayons X et par thermogravimetrie, permettent de proposer une hypothese sur les proprietes de l'oxyde obtenu. Dans la deuxieme partie, les auteurs developpent un calcul prevoyant la marche continue de cellules uniques et en cascades. De ces calculs on tire les elements permettant la realisation de deux cellules de 0,3 et 10 litres. Des resultats de marche continue sur cette derniere cellule, on peut conclure a l'applicabilite de cette methode a l'hydrometallurgie de l'uranium. (auteurs)

A fuel-cell reactor for the direct synthesis of hydrogen peroxide alkaline solutions from H(2) and O(2).

Science.gov (United States)

Yamanaka, Ichiro; Onisawa, Takeshi; Hashimoto, Toshikazu; Murayama, Toru

2011-04-18

The effects of the type of fuel-cell reactors (undivided or divided by cation- and anion-exchange membranes), alkaline electrolytes (LiOH, NaOH, KOH), vapor-grown carbon fiber (VGCF) cathode components (additives: none, activated carbon, Valcan XC72, Black Pearls 2000, Seast-6, and Ketjen Black), and the flow rates of anolyte (0, 1.5, 12 mL h(-1)) and catholyte (0, 12 mL h(-1)) on the formation of hydrogen peroxide were studied. A divided fuel-cell system, O(2) (g)|VGCF-XC72 cathode|2 M NaOH catholyte|cation-exchange membrane (Nafion-117)|Pt/XC72-VGCF anode|2 M NaOH anolyte at 12 mL h(-1) flow|H(2) (g), was effective for the selective formation of hydrogen peroxide, with 130 mA cm(-2) , a 2 M aqueous solution of H(2)O(2)/NaOH, and a current efficiency of 95 % at atmospheric pressure and 298 K. The current and formation rate gradually decreased over a long period of time. The cause of the slow decrease in electrocatalytic performance was revealed and the decrease was stopped by a flow of catholyte. Cyclic voltammetry studies at the VGCF-XC72 electrode indicated that fast diffusion of O(2) from the gas phase to the electrode, and quick desorption of hydrogen peroxide from the electrode to the electrolyte were essential for the efficient formation of solutions of H(2)O(2)/NaOH. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

High-performance oxygen reduction catalysts in both alkaline and acidic fuel cells based on pre-treating carbon material and iron precursor

Energy Technology Data Exchange (ETDEWEB)

Song, Ping; Barkholtz, Heather M.; Wang, Ying; Xu, Weilin; Liu, Dijia; Zhuang, Lin

2017-12-01

We demonstrate a new and simple method for pre-treating the carbon material and iron precursor to prepare oxygen reduction reaction (ORR) catalysts, which can produce super-high performance and stability in alkaline solution, with high performance in acid solution. This strategy using cheap materials is simply controllable. Moreover, it has achieved smaller uniform nanoparticles to exhibit high stability, and the synergetic effect of Fe and N offered much higher performance in ORR than commercial Pt/C, with high maximum power density in alkaline and acid fuel cell test. So it can make this kind of catalysts be the most promising alternatives of Pt-based catalysts with best performance/price.

Thermodynamic framework for estimating the efficiencies of alkaline batteries

Energy Technology Data Exchange (ETDEWEB)

Pound, B G; Singh, R P; MacDonald, D D

1986-06-01

A thermodynamic framework has been developed to evaluate the efficiencies of alkaline battery systems for electrolyte (MOH) concentrations from 1 to 8 mol kg/sup -1/ and over the temperature range -10 to 120/sup 0/C. An analysis of the thermodynamic properties of concentrated LiOH, NaOH, and KOH solutions was carried out to provide data for the activity of water, the activity coefficient of the hydroxide ion, and the pH of the electrolyte. Potential-pH relations were then derived for various equilibrium phenomena for the metals Li, Al, Fe, Ni, and Zn in aqueous solutions and, using the data for the alkali metal hydroxides, equilibrium potentials were computed as a function of composition and temperature. These data were then used to calculate reversible cell voltages for a number of battery systems, assuming a knowledge of the cell reactions. Finally, some of the calculated cell voltages were compared with observed cell voltages to compute voltage efficiencies for various alkaline batteries. The voltage efficiencies of H/sub 2//Ni, Fe/Ni, and Zn/Ni test cells were found to be between 90 and 100%, implying that, at least at open circuit, there is little, if any, contribution from parasitic redox couples to the cell potentials for these systems. The efficiency of an Fe/air test cell was relatively low (72%). This is probably due to the less-than-theoretical voltage of the air electrode.

Anditalea andensis ANESC-ST--An Alkaliphilic Halotolerant Bacterium Capable of Electricity Generation under Alkaline-Saline Conditions.

Directory of Open Access Journals (Sweden)

Wei Shi

Full Text Available A great challenge in wastewater bioremediation is the sustained activity of viable microorganisms, which can contribute to the breakdown of waste contaminants, especially in alkaline pH conditions. Identification of extremophiles with bioremediation capability can improve the efficiency of wastewater treatment. Here, we report the discovery of an electrochemically active alkaliphilic halotolerant bacterium, Anditalea andensis ANESC-ST (=CICC10485T=NCCB 100412T, which is capable of generating bioelectricity in alkaline-saline conditions. A. andensis ANESC-ST was shown to grow in alkaline conditions between pH 7.0-11.0 and also under high salt condition (up to 4 wt% NaCl. Electrical output was further demonstrated in microbial fuel cells (MFCs with an average current density of ~0.5 µA/cm2, even under the harsh condition of 4 wt% NaCl and pH 9.0. Subsequent introduction of secreted extracellular metabolites into MFCs inoculated with Escherichia coli or Pseudomonas aeruginosa yielded enhanced electrical output. The ability of A. andensis ANESC-ST to generate energy under alkaline-saline conditions points towards a solution for bioelectricity recovery from alkaline-saline wastewater. This is the first report of A.andensis ANESC-ST producing bioelectricity at high salt concentration and pH.

Permeability change with dissolution and precipitation reaction induced by highly alkaline plume in packed bed with amorphous silica particles

International Nuclear Information System (INIS)

Komatsu, Kyo; Kadowaki, Junichi; Niibori, Yuichi; Mimura, Hitoshi; Usui, Hideo

2008-01-01

A large amount of cement is used to construct of the geological disposal system. Such a material alters the pH of groundwater to highly alkaline region. The highly alkaline plume contains rich Ca ion compared to the surrounding environment, and the Ca ion reacts with soluble silicic acid. Its product would deposit on the surface of flow-paths in the natural barrier and decrease the permeability. In this study, the influence of Ca ions in highly alkaline plume on flow-paths has been examined by using packed bed column. The column was packed with the amorphous silica particles of 75-150 μm in diameter. The Ca(OH) 2 solution (0.78 mM, 2.58 mM, 4.37 mM, and 8.48 mM, pH: 12.2-12.4) was continuously injected into the column at a constant flow rate (5 ml/min, and 2 ml/min), and the change of permeability was monitored. At the same time, the concentrations of [Ca] total and [Si] in the eluted solution were measured by the inductively coupled plasma atomic emission spectrometry (ICP-AES). The Ca(OH) 2 solutions were prepared with CO 2 -free pure water, and filtrated through 0.45 μm filter. The permeability was normalized by the initial permeability value. In the experiment results, the permeability dramatically changed with increasing Ca concentration, because Ca ions and H 4 SiO 4 (due to the dissolution of SiO 2 ) produce C-S-H gel between the packed particles in the column. The SEM images and XRD analyses showed that the surface of SiO 2 particles was covered with the C-S-H gel precipitation. On the other hand, when the Ca concentration was relatively low, the permeability did not show remarkable change. For the cross section of SiO 2 particles, EPMA analysis suggested the consumption of Ca in the inner pore of the SiO 2 particles. However, the time-change in the concentrations of Si and Ca was not always simple. Such time-change strongly depended not only on pH or Ca concentration, but also on the flow rates. This suggested that mass transport controls the chemical

A single pH fluorescent probe for biosensing and imaging of extreme acidity and extreme alkalinity.

Science.gov (United States)

Chao, Jian-Bin; Wang, Hui-Juan; Zhang, Yong-Bin; Li, Zhi-Qing; Liu, Yu-Hong; Huo, Fang-Jun; Yin, Cai-Xia; Shi, Ya-Wei; Wang, Juan-Juan

2017-07-04

A simple tailor-made pH fluorescent probe 2-benzothiazole (N-ethylcarbazole-3-yl) hydrazone (Probe) is facilely synthesized by the condensation reaction of 2-hydrazinobenzothiazole with N-ethylcarbazole-3-formaldehyde, which is a useful fluorescent probe for monitoring extremely acidic and alkaline pH, quantitatively. The pH titrations indicate that Probe displays a remarkable emission enhancement with a pK a of 2.73 and responds linearly to minor pH fluctuations within the extremely acidic range of 2.21-3.30. Interestingly, Probe also exhibits strong pH-dependent characteristics with pK a 11.28 and linear response to extreme-alkalinity range of 10.41-12.43. In addition, Probe shows a large Stokes shift of 84 nm under extremely acidic and alkaline conditions, high selectivity, excellent sensitivity, good water-solubility and fine stability, all of which are favorable for intracellular pH imaging. The probe is further successfully applied to image extremely acidic and alkaline pH values fluctuations in E. coli cells. Copyright © 2017 Elsevier B.V. All rights reserved.

Calculated solubility isotherm of a system of alkaline earth sulfates and hydroxides in water

International Nuclear Information System (INIS)

MOshinskii, A.S.; TIkomirova, K.A.

1986-01-01

Tis paper examines the calculation of the isothermal solubility diagram of a system of alkaline earth sulfates and hydroxides in water which makes it possible to substantiate, to a considerable extent, the natural physicochemical mineralization of natural waters, in particular water from geochemical sources. The present paper investigates the solubility of the equilibrium solid phases of a system of alkaline earth sulfates and hydroxides in water. A projection is shown of the composition prism of the quinary reciprocal system with demarcation of the crystallization areas of each sulfate and hydroxide of the component subsystems. The computational formulas for calculating solubility were derived from the solubility product principle, with allowance for ion activity coefficients in saturated hydroxide solutions

Influence of media composition on the production of alkaline α-amylase from Bacillus subtilis CB-18.

Science.gov (United States)

Ogbonnaya, Nwokoro; Odiase, Anthonia

2012-01-01

Starch, a homopolysaccharide is an important and an abundant food reserve and energy source. Starches are processed to yield different products which find many industrial applications. Alpha-amylases hydrolyze starch by cleaving α-1,4-glucosidic bonds and have been used in food, textile and pharmaceutical industries [Sun et al. 2010]. Enzymatic conversion of starch with amylase presents an economically superior alternative to the conventional method of starch gelatinization. Alkaline α-amylase has an important position in the global enzyme market as a constituent of detergent. In this paper, we screened soil bacteria and an isolate, alkalophilic Bacillus subtilis CB-18 was found to produce an alkaline α-amylase in different media. MATERIAL AND METHODS. Screening of the isolates for amylolytic activity was carried out by growing bacteria isolated from the soil in starch agar plates and subsequently staining the plates with iodine solution to reveal zones of hydrolysis of starch. The selected isolate, Bacillus subtlis CB-18 was grown in different media at alkaline pH to evaluate the influence of media composition on alkaline α-amylase production. Enzyme assay was carried out by growing the culture in a broth medium and obtaining cell - free culture supernatant after centrifugation at 2515 × g for 15 minutes Amylase activity was determined by incubating 0.5 ml of crude enzyme solution in 0.1M Tris/HCl buffer (pH 8.5) with 0.5 ml of 1% soluble starch solution. The reaction was terminated by the addition of DNS reagent and reducing sugar produced from the amylolytic reaction was determined. Bacillus subtilis CB-18 used for this work was selected because it produced 7 mm zone diameter on starch agar plate. This organism was cultured in different alkaline broth media containing 2% soluble starch as inducer carbohydrate for α-amylase production. Among the carbon sources used for enzyme production, sorbitol was the best to stimulate enzyme production with �

Dissolution characteristics of chalcedony under alkaline condition. Study for changes in mineral composition of engineered barrier composed by bentonite

International Nuclear Information System (INIS)

Watanabe, Yasutaka; Yokoyama, Shingo

2016-01-01

In the engineered barrier of radioactive waste disposal facilities, it is expected that bentonite is exposed to alkaline groundwater which arise from leaching of cementations materials. Minerals contained in the bentonite will be dissolved by reactions of the alkaline groundwater. Some bentonite contains silica such as quartz and chalcedony. Chalcedony is categorized in intermediate silica which is microcrystalline. It is known that dissolution of silica influences to the dissolution of smectite by means of solubility. However, dissolution kinetics of chalcedony in the alkaline condition has not been investigated, which is an uncertainty in geochemical simulations to evaluate a long-term stability of the engineered barrier. Therefore, this study performed flow-through experiments in alkaline conditions using chalcedony in order to obtain the dissolution rate of the chalcedony. The flow-through experiments was performed using NaOH-NaCl solution adjusted to 0.3 mol/L of ionic strength. Initial pH of the solution was from 8.9 to 13.5. As a result, higher pH and higher temperature showed higher Si ion concentrations of reacted solutions. The dissolution rate of the samples was calculated using Si ion concentrations at steady state of the experiment. Note that, the dissolution rate of the chalcedony was almost same as that of quartz at same temperature. After the experiments, SEM observation showed that rough surface of the chalcedony partly changed to smooth surface like quartz. It is supposed that rough surface of chalcedony was rapidly dissolved because of low degree of crystallization. The dissolution rate obtained is supposedly applicable to highly crystalline SiO 2 of chalcedony. (author)

Applicability of low alkaline cement for construction and alteration of bentonite in the cement. 2

International Nuclear Information System (INIS)

Iriya, Keishiro; Fujii, Kensuke; Tajima, Takatoshi; Takeda, N.; Kubo, Hiroshi

2003-02-01

This study consists of accelerating corrosion test of rebar in saline, automogeneous shrinkage test of HFSC, accelerating test for bentonite and rock, and summarizing rock and bentonite alteration. Corrosion of rebars in HFSC: Since sorption capacity of HFSC for Cl ion is slow due to low alkalinity, rate of corrosion of rebar in HFSC is very large. Cracking due to corrosion is generating in 4 years or 20 years, although service period is deferent in OPC amount. Automogenous shrinkage: Automogenous shrinkage of HFSC is larger than OPC in cement paste. It decreases corresponding to rise of fly ash content. The shrinkage in HFSC 226 is quite similar to OPC. The shrinkage in HFSC concrete is smaller than OPC concrete. 720 days alteration test of bentonite by solution of low alkaline cement: Ion exchange to Ca bentonite and calcite are observed in the solid phase. Thin plate of bentonite is disappeared and round shaped secondary mineral is generated. Dissolution of bentonite and generation of secondary minerals are limited in pH 11.0 or less, since pH of bentonite is about 10.0. 720 days alteration test of rock by solution of low alkaline cement: Calcite is generated in very test. Very small evidence is observed as generation of secondary minerals. Etched pits are observed in tuff A due to corrosion. (author)

Study of poly(vinyl alcohol)/titanium oxide composite polymer membranes and their application on alkaline direct alcohol fuel cell

Science.gov (United States)

Yang, Chun-Chen; Chiu, Shwu-Jer; Lee, Kuo-Tong; Chien, Wen-Chen; Lin, Che-Tseng; Huang, Ching-An

The novel poly(vinyl alcohol)/titanium oxide (PVA/TiO 2) composite polymer membrane was prepared using a solution casting method. The characteristic properties of the PVA/TiO 2 composite polymer membrane were investigated by thermal gravimetric analysis (TGA), a scanning electron microscopy (SEM), a micro-Raman spectroscopy, a methanol permeability measurement and the AC impedance method. An alkaline direct alcohol (methanol, ethanol and isopropanol) fuel cell (DAFC), consisting of an air cathode based on MnO 2/C inks, an anode based on PtRu (1:1) black and a PVA/TiO 2 composite polymer membrane, was assembled and examined for the first time. The results indicate that the alkaline DAFC comprised of a cheap, non-perfluorinated PVA/TiO 2 composite polymer membrane shows an improved electrochemical performances. The maximum power densities of alkaline DAFCs with 4 M KOH + 2 M CH 3OH, 2 M C 2H 5OH and 2 M isopropanol (IPA) solutions at room temperature and ambient air are 9.25, 8.00, and 5.45 mW cm -2, respectively. As a result, methanol shows the highest maximum power density among three alcohols. The PVA/TiO 2 composite polymer membrane with the permeability values in the order of 10 -7 to 10 -8 cm 2 s -1 is a potential candidate for use on alkaline DAFCs.

Copper and brass aged at open circuit potential in slightly alkaline solutions

International Nuclear Information System (INIS)

Procaccini, R.; Vazquez, M.; Cere, S.

2009-01-01

Surface oxide films were grown on 99.99% copper and brass (copper-zinc alloy, Cu77Zn21Al2) in 0.1 mol L -1 borax solution at open circuit potential and were characterized using various experimental techniques. The composition of the passive films formed in situ on the different materials was studied using differential reflectance spectroscopy. The thickness of the oxide layers on copper and brass was compared by chronopotentiometric curves and potentiodynamic reductions. The electrical properties of each oxide were analyzed by means of electrochemical impedance spectroscopy. Their influence on the oxygen reduction reaction was also investigated using voltammetry hydrodynamic tools such as the rotating disk electrode. The results show that the incorporation of Zn to Cu in brass changes the composition and the thickness of the surface film. The films grown on brass tend to be thicker but less resistive and Zn compounds incorporate to the film. This is supported by results from reflectance and impedance spectroscopy. The kinetics of oxygen reduction is strongly inhibited on oxidized electrodes, particularly in the case of brass. The global number of exchanged electrons remains close to four and seems to be independent of the presence of surface oxides.

Fragile to strong crossover at the Widom line in supercooled aqueous solutions of NaCl

Energy Technology Data Exchange (ETDEWEB)

Gallo, P. [Dipartimento di Matematica e Fisica, Università Roma Tre, Via della Vasca Navale 84, I-00146 Rome, Italy and INFN, Sezione di Roma Tre, Via della Vasca Navale 84, I-00146 Rome (Italy); Corradini, D.; Rovere, M., E-mail: rovere@fis.uniroma3.it [Dipartimento di Matematica e Fisica, Università Roma Tre, Via della Vasca Navale 84, I-00146 Rome (Italy)

2013-11-28

We study by molecular dynamics simulations the dynamical properties of an aqueous solution of NaCl at a concentration of 0.67 mol/kg upon supercooling. In a previous study of the same ionic solution, we have located the liquid-liquid critical point (LLCP) and determined the Widom line connected to the liquid-liquid transition. We present here the results obtained from the study of the self-intermediate scattering function in a large range of temperatures and densities approaching the LLCP. The structural relaxation is in agreement with the mode coupling theory (MCT) in the region of mild supercooling. In the deeper supercooled region the α-relaxation time as function of temperature deviates from the MCT power law prediction showing a crossover from a fragile to a strong behavior. This crossover is found upon crossing the Widom line. The same trend was found in bulk water upon supercooling and it appears almost unchanged by the interaction with ions apart from a shift in the thermodynamic plane toward lower pressures and higher temperatures. These results show that the phenomenology of supercooled water transfers from bulk to solution where the study of the supercooled region is experimentally less difficult.

Pit morphology studies of iron and steel in alkaline chloride environment using EMPA technique

International Nuclear Information System (INIS)

Benjamin, S.E.; Sykes, J.M.

1993-01-01

A comparative study of iron and steel in stimulated alkaline chloride solutions showed that Swedish iron has better reproducibility in terms of pitting potentials as compared to ordinary hot rolled mild steel. This study was undertaken to reason this pitting behavior on the basis of number and the nature of inclusions present in both the metals. Electron probe microanalysis technique (EPMA) was utilised to contemplate the origin of pits, the solution chemistry of the pits and finally the nature of the rust product. (author)

Quaternized poly(vinyl alcohol)/alumina composite polymer membranes for alkaline direct methanol fuel cells

Science.gov (United States)

Yang, Chun-Chen; Chiu, Shwu-Jer; Chien, Wen-Chen; Chiu, Sheng-Shin

The quaternized poly(vinyl alcohol)/alumina (designated as QPVA/Al 2O 3) nanocomposite polymer membrane was prepared by a solution casting method. The characteristic properties of the QPVA/Al 2O 3 nanocomposite polymer membranes were investigated using thermal gravimetric analysis (TGA), scanning electron microscopy (SEM), dynamic mechanical analysis (DMA), micro-Raman spectroscopy, and AC impedance method. Alkaline direct methanol fuel cell (ADMFC) comprised of the QPVA/Al 2O 3 nanocomposite polymer membrane were assembled and examined. Experimental results indicate that the DMFC employing a cheap non-perfluorinated (QPVA/Al 2O 3) nanocomposite polymer membrane shows excellent electrochemical performances. The peak power densities of the DMFC with 4 M KOH + 1 M CH 3OH, 2 M CH 3OH, and 4 M CH 3OH solutions are 28.33, 32.40, and 36.15 mW cm -2, respectively, at room temperature and in ambient air. The QPVA/Al 2O 3 nanocomposite polymer membranes constitute a viable candidate for applications on alkaline DMFC.

Characterization of commercial iron chelates and their behavior in an alkaline and calcareous soil.

Science.gov (United States)

Cantera, Rodrigo G; Zamarreño, Angel M; García-Mina, José M

2002-12-18

Iron deficiency is a common problem for many plants grown in alkaline and calcareous soils. To correct this problem, iron is supplied to plants as chelates. Several iron chelates are sold under diverse trademarks with different characteristics. This work evaluated 18 commercial products containing the most representative chelated iron sources used in agricultural practice in Spain when the study was done, namely the ferric chelates of EDDHA, EDDHMA, EDDCHA, EDDHSA, EDTA, and DTPA. The chelates were comprehensively characterized and quantitated by several techniques, including several chromatographic methods. Iron and chelate dynamics in soil were also studied in a model alkaline and calcareous soil. Results indicate that, in this model soil, among the different iron compounds studied only FeEDDHA and analogues have the capacity to maintain soluble iron in soil solution over time. These results are in agreement with general experience under field conditions. Furthermore, among the different ortho-ortho isomers of FeEDDHA's, FeEDDHSA and FeEDDCHA showed greater capacity than FeEDDHA and FeEDDHMA to maintain the chelated iron in soil solution over time.

Neutralization of acid mine drainage using the final product from CO2 emissions capture with alkaline paper mill waste

International Nuclear Information System (INIS)

Perez-Lopez, Rafael; Castillo, Julio; Quispe, Dino; Nieto, Jose Miguel

2010-01-01

In this study, experiments were conducted to investigate the applicability of low-cost alkaline paper mill wastes as acidity neutralizing agents for treatment of acid mine drainage (AMD). Paper wastes include a calcium mud by-product from kraft pulping, and a calcite powder from a previous study focused on sequestering CO 2 by carbonation of calcium mud. The neutralization process consisted of increase of pH by alkaline additive dissolution, decrease of metals solubility and precipitation of gypsum and poorly crystallized Fe-Al oxy-hydroxides/oxy-hydroxysulphates, which acted as a sink for trace elements to that extent that solutions reached the pre-potability requirements of water for human consumption. This improvement was supported by geochemical modelling of solutions using PHREEQC software, and observations by scanning electron microscope and X-ray diffraction of reaction products. According to PHREEQC simulations, the annual amount of alkaline additive is able to treat AMD (pH 3.63, sulphate 3800 mg L -1 , iron 348 mg L -1 ) with an average discharge of about 114 and 40 L s -1 for calcium mud and calcite powder, respectively. Likewise, given the high potential of calcium mud to sequester CO 2 and of resulting calcite powder to neutralize AMD, paper wastes could be a promising solution for facing this double environmental problem.

Electro chemical studies on stress corrosion cracking of Incoloy-800 in caustic solution, part I: As received samples

Directory of Open Access Journals (Sweden)

Dinu Alice

2005-01-01

Full Text Available Many non-volatile impurities accidentally introduced into the steam generator tend to Concentrate on its surface in restricted flow areas. In this way these impurities can lead to stress corrosion cracking (SCC on stressed tubes of the steam generator. Such impurities can be strong alkaline or acid solutions. To evaluate the effect of alkaline concentrated environments on SCC of steam generator tubes, the tests were con ducted on stressed samples of Incoloy-800 in 10% NaOH solution. To accelerate the SCC process, stressed specimens were anodically polarised in a caustic solution in an electro chemical cell. The method of stressing of Incoloy-800 tubes used in our experiments was the C-ring. Using the cathodic zone of the potentiodynamic curves it was possible to calculate the most important electrochemical parameters: the corrosion current, the corrosion rate, and the polarization resistance. We found that the value of the corrosion potential to initiate the SCC microcracks was -100 mV. The tested samples were examined using the metallographic method. The main experimental results showed that the in crease of the stress state promoted the in crease of the SCC susceptibility of Incoloy-800 samples tested under the same conditions, and that the length of the SCC-type microcracks in creased with the growth of the stress value.

Petrological and geochemical studies of alkaline rocks from continental Brazil. 8. The syenitic intrusion of Morro Redondo, RJ

International Nuclear Information System (INIS)

Brotzu, P.; Melluso, L.; Beccaluva, L.

1989-01-01

The alkaline complex of Morro Redondo is mainly composed of syenites, alkali syenites and nepheline syenites. The age of the intrusion, utilizing eleven newly available K/Ar data, is about 73 Ma. Petrography, mineral chemistry and geochemistry strongly support cogeneticity among the various lithotypes, linked by fractional crystallisation of the observed phases and crystal accumulation, preferentially of alkali feldspar. Initial Sr isotopic ratios indicate a mantle parental magma, probably generated in the subcontinental lithosphere, like other Brazilian alkaline complexes (e.g. Fortaleza, Juquia, Piratini, Tunas). (author) [pt

The anodic dissolution of zinc and zinc alloys in alkaline solution. II. Al and Zn partial dissolution from 5% Al–Zn coatings

International Nuclear Information System (INIS)

Vu, T.N.; Mokaddem, M.; Volovitch, P.; Ogle, K.

2012-01-01

Graphical abstract: - Abstract: The polarization behavior of a 5 wt% Al–Zn steel coating (Galfan™) has been investigated in alkaline solution using atomic emission spectroelectrochemistry (AESEC). The instantaneous Zn and Al dissolution rates were measured as a function of time during a linear scan and potential step transients. The formation rate of insoluble oxides was determined from the difference between the convoluted total current and the sum of the elemental dissolution currents. It was found that, over a wide potential range, the zinc and aluminum partial currents behaved in a similar way to pure zinc and pure aluminum independently. However, during the period in which zinc was active, aluminum dissolution was inhibited. This is attributed to the inhibitive effect of the first and/or the second states of zinc oxide that are formed during the active potential domain. The third form of zinc oxide, observed at higher potential and responsible for the passivation of zinc dissolution, does not have a measurable effect on the Al dissolution rate.

Ethylenediaminetetraacetates of neodymium and alkaline earth metals

International Nuclear Information System (INIS)

Barinov, A.V.; Pechurova, L.I.; Martynenko, K.I.; Popov, K.I.; Spitsyn, V.I.

1977-01-01

The possibilities have been studied of the formation of polynuclear complexonates of alkaline-earth metals (Ca, Sr, and Ba) based on neodymium derivatives EDTA of the composition NdA - . By pH-metry, electron spectroscopy, and derivatography it has been shown that the structure of complexes M 2 (NdA) 2 (where M- Ca, Sr, or Ba; A- EDTA) in the solution is not polynuclear. Hydroxopolynuclear complexes do not form under conditions studied. The data obtained agree with an assumption about polynuclear structure of the solid complex Ca(NdA) 2 x17 H 2 O and gradual weakening of the polynuclear nature upon substitution of Ca 2+ with Sr 2+ and Ba 2+

Using solute and heat tracers for aquifer characterization in a strongly heterogeneous alluvial aquifer

Science.gov (United States)

Sarris, Theo S.; Close, Murray; Abraham, Phillip

2018-03-01

A test using Rhodamine WT and heat as tracers, conducted over a 78 day period in a strongly heterogeneous alluvial aquifer, was used to evaluate the utility of the combined observation dataset for aquifer characterization. A highly parameterized model was inverted, with concentration and temperature time-series as calibration targets. Groundwater heads recorded during the experiment were boundary dependent and were ignored during the inversion process. The inverted model produced a high resolution depiction of the hydraulic conductivity and porosity fields. Statistical properties of these fields are in very good agreement with estimates from previous studies at the site. Spatially distributed sensitivity analysis suggests that both solute and heat transport were most sensitive to the hydraulic conductivity and porosity fields and less sensitive to dispersivity and thermal distribution factor, with sensitivity to porosity greatly reducing outside the monitored area. The issues of model over-parameterization and non-uniqueness are addressed through identifiability analysis. Longitudinal dispersivity and thermal distribution factor are highly identifiable, however spatially distributed parameters are only identifiable near the injection point. Temperature related density effects became observable for both heat and solute, as the temperature anomaly increased above 12 degrees centigrade, and affected down gradient propagation. Finally we demonstrate that high frequency and spatially dense temperature data cannot inform a dual porosity model in the absence of frequent solute concentration measurements.

Cellulose Degradation at Alkaline Conditions: Long-Term Experiments at Elevated Temperatures

International Nuclear Information System (INIS)

Glaus, M.A.; Van Loon, L.R.

2004-04-01

temperatures tested here. It may be hypothesised that the alkaline hydrolysis has even not been observed in the experiments. However, if this is true, cellulose degradation proceeded via another unknown type of reaction. Mass balances for carbon show that the large majority of reaction products found in solution can be explained by formation of isosaccharinic acids and other low-molecular weight carboxylic acids. With respect to long-term predictions for cellulose degradation at room temperature it can be concluded that the kinetic parameters for alkaline hydrolysis as proposed in the work of PAVASARS (Linkoping Studies in Arts and Science, 196, Linkoping University, Sweden, 1999) are too large and that complete cellulose degradation at these temperatures occurs only within time scales larger than hundreds of years. However, it is not possible from the experimental evidences, to corroborate the validity of a linear extrapolation (Arrhenius equation) of the reaction rates measured at temperatures between 140 and 190 o C to room temperature, from which it was previously concluded that complete cellulose degradation would take time spans of the order of millions of years. An interesting observation in the present experiments is the chemical instability of aisosaccharinic acid at 90 o C, which has been hypothetically interpreted as a fragmentation induced by the sorption of α-isosaccharinic acid on Ca(OH) 2 . Carbon mass balances show that α-isosaccharinic acid is thereby transformed to other lowmolecular weight carboxylic acids. Such a reaction would be an interesting long-term perspective for performance assessment of the disposal of cellulose-containing radioactive waste, in that it may reduce the concentration of organic compounds strongly complexing radionuclides. (author)

Cellulose Degradation at Alkaline Conditions: Long-Term Experiments at Elevated Temperatures

Energy Technology Data Exchange (ETDEWEB)

Glaus, M.A.; Van Loon, L.R

2004-04-01

hydrolysis at the temperatures tested here. It may be hypothesised that the alkaline hydrolysis has even not been observed in the experiments. However, if this is true, cellulose degradation proceeded via another unknown type of reaction. Mass balances for carbon show that the large majority of reaction products found in solution can be explained by formation of isosaccharinic acids and other low-molecular weight carboxylic acids. With respect to long-term predictions for cellulose degradation at room temperature it can be concluded that the kinetic parameters for alkaline hydrolysis as proposed in the work of PAVASARS (Linkoping Studies in Arts and Science, 196, Linkoping University, Sweden, 1999) are too large and that complete cellulose degradation at these temperatures occurs only within time scales larger than hundreds of years. However, it is not possible from the experimental evidences, to corroborate the validity of a linear extrapolation (Arrhenius equation) of the reaction rates measured at temperatures between 140 and 190{sup o}C to room temperature, from which it was previously concluded that complete cellulose degradation would take time spans of the order of millions of years. An interesting observation in the present experiments is the chemical instability of aisosaccharinic acid at 90{sup o}C, which has been hypothetically interpreted as a fragmentation induced by the sorption of {alpha}-isosaccharinic acid on Ca(OH){sub 2}. Carbon mass balances show that {alpha}-isosaccharinic acid is thereby transformed to other lowmolecular weight carboxylic acids. Such a reaction would be an interesting long-term perspective for performance assessment of the disposal of cellulose-containing radioactive waste, in that it may reduce the concentration of organic compounds strongly complexing radionuclides. (author)

Long term behaviour of compacted argillite submitted to an alkaline fluid circulation

International Nuclear Information System (INIS)

Cuisinier, O.; Masrouri, F.; Deneele, Dimitri

2010-01-01

Document available in extended abstract form only. In the French concept of deep nuclear wastes repository, the galleries should be backfilled with excavated argillite after the site exploitation period. After several thousands of years, the degradation of the concrete lining of the galleries will generate alkaline fluid (pH > 12) that will diffuse through the backfill. The object of the study is to describe the influence of such solute diffusion on the microstructure of compacted argillite. Saturated-portlandite water was circulated through compacted samples for 3, 6 and 12 months at 20 or 60 deg. C. First, the mechanical behaviour of the samples was determined after the fluid circulation period. The microstructure of the samples was also analysed via mercury intrusion porosimetry tests, scanning electron microscopy and optical microscopy. Since it is planned to introduce additives (bentonite, calcareous sand or lime) in the remoulded argillite to backfill the deep galleries, such mixtures were also studied. The results showed that MA particles are sensitive to the alkaline fluid circulation at the microstructural level. In the case of the calcareous sand, no major changes of the microstructure nor the mechanical behaviour were observed. The pure argillite underwent slight modifications that can be related to a limited dissolution of its clayey particles. Conversely, intense alteration of the MX-80 particles was evidenced with a strong increase of the macro-pore void ration while the mechanical behaviour was slightly altered by the fluid circulation. Lime addition improved the mechanical characteristics of the argillite through the precipitation of cementitious compounds. The microstructure of the lime-treated argillite was also altered by the fluid circulation. That study evidenced that alkaline fluid circulation led to the dissolution clayey particles, leading to the increase of the macro-pore void ratio. Some of the dissolved compounds allowed the formation of

KINETICS OF THE HYDROXYPROPYLATION OF POTATO STARCH IN AQUEOUS-SOLUTION

NARCIS (Netherlands)

LAMMERS, G; STAMHUIS, EJ; BEENACKERS, AACM

Kinetic results are presented for the hydroxypropylation of Potato starch with methyloxirane in aqueous solution. Reaction temperatures were varied from 303 to 362 K. Sodium hydroxide was used as a catalyst. The overall conversion rate of methyloxirane in alkaline starch solution is determined by

Nitrate removal from alkaline high nitrate effluent by in situ generation of hydrogen using zinc dust

International Nuclear Information System (INIS)

Rajagopal, S.; Chitra, S.; Paul, Biplob

2016-01-01

Alkaline radioactive low level waste generated in Nuclear Fuel Cycle contains substantial amount of nitrate and needs to be treated to meet Central Pollution Control Board discharge limits of 90 mg/L in marine coastal area. Several denitrification methods like chemical treatment, electrochemical reduction, biological denitrification, ion exchange, reverse osmosis, photochemical reduction etc are followed for removal of nitrate. In effluent treatment plants where chemical treatment is carried out, chemical denitrification can be easily adapted without any additional set up. Reducing agents like zinc and aluminum are suitable for reducing nitrate in alkaline solution. Study on denitrification with zinc dust was taken up in this work. Not much work has been done with zinc dust on reduction of nitrate to nitrogen in alkaline waste with high nitrate content. In the present work, nitrate is reduced by nascent hydrogen generated in situ, caused by reaction between zinc dust and sodium hydroxide

Chitosan-ferrocyanide sorbent for Cs-137 removal from mineralized alkaline media

Energy Technology Data Exchange (ETDEWEB)

Egorin, Andrei [Far Eastern Federal Univ., Vladivostok (Russian Federation); Institute of Chemistry FEBRAS, Vladivostok (Russian Federation); Ozyorsk Technical Institute MEPHI, Ozersk (Russian Federation); Tokar, Eduard [Far Eastern Federal Univ., Vladivostok (Russian Federation); Zemskova, Larisa [Institute of Chemistry FEBRAS, Vladivostok (Russian Federation)

2016-11-01

An organomineral sorbent based on mixed nickel-potassium ferrocyanide and chitosan to be used in removal of Cs-137 radionuclide from highly mineralized media with high pH has been fabricated. The synthesized sorbent was applied to remove Cs-137 from model solutions under static and dynamic conditions. The effects of contact time, pH, and presence of sodium ions and complexing agents in the process of Cs-137 removal have been investigated. The sorbent is distinguished by increased stability to the impact of alkaline media containing complexing agents, whereas the sorbent capacity in solutions with pH 11 exceeds 1000 bed volumes with the Cs-137 removal efficiency higher than 95%.

A novel solution to the Klein–Gordon equation in the presence of a strong rotating electric field

Energy Technology Data Exchange (ETDEWEB)

Raicher, E., E-mail: erez.raicher@mail.huji.ac.il [Racah Institute of Physics, Hebrew University, Jerusalem 91904 (Israel); Department of Applied Physics, Soreq Nuclear Research Center, Yavne 81800 (Israel); Eliezer, S. [Department of Applied Physics, Soreq Nuclear Research Center, Yavne 81800 (Israel); Nuclear Fusion Institute, Polytechnic University of Madrid, Madrid (Spain); Zigler, A. [Racah Institute of Physics, Hebrew University, Jerusalem 91904 (Israel)

2015-11-12

The Klein–Gordon equation in the presence of a strong electric field, taking the form of the Mathieu equation, is studied. A novel analytical solution is derived for particles whose asymptotic energy is much lower or much higher than the electromagnetic field amplitude. The condition for which the new solution recovers the familiar Volkov wavefunction naturally follows. When not satisfied, significant deviation from the Volkov wavefunction is demonstrated. The new condition is shown to differ by orders of magnitudes from the commonly used one. As this equation describes (neglecting spin effects) the emission processes and the particle motion in Quantum Electrodynamics (QED) cascades, our results suggest that the standard theoretical approach towards this phenomenon should be revised.

Removal of six pesticide residues in cowpea with alkaline electrolysed water.

Science.gov (United States)

Han, Yongtao; Song, Le; An, Quanshun; Pan, Canping

2017-06-01

Reduction of six pesticide residues (isoprocarb, chlorpyrifos, bifenthrin, beta-cypermethrin, difenoconazole and azoxystrobin) in cowpea by alkaline electrolysed water (AlEW) solutions with different pH was investigated. The commonly used washing treatments in household processing were used for comparison. The residue magnitudes were determined by gas chromatography coupled with tandem mass spectrometry (GC-MS/MS). Results showed that the removal effect of AlEW solution on the six pesticides was superior to tap water, 5% sodium chloride, 5% sodium carbonate and 5% acetic acid solution. AlEW with pH 12.2 had more potential to eliminate the six pesticides in cowpeas. Moreover, the reduction of pesticide residues gradually increased with the increase of washing time. This study demonstrated that AlEW solution with pH of 12.2 could be used to reduce pesticide residues on fresh cowpea samples. © 2016 Society of Chemical Industry. © 2016 Society of Chemical Industry.

Wear and chemistry of zirconium-silicate, aluminium-silicate and zirconium-aluminium-silicate glasses in alkaline medium

International Nuclear Information System (INIS)

Rouse, C.G.; Lemos Guenaga, C.M. de

1984-01-01

A study of the chemical durability, in alkaline solutions, of zirconium silicate, aluminium silicate, zirconium/aluminium silicate glasses as a function of glass composition is carried out. The glasses were tested using standard DIN-52322 method, where the glass samples are prepared in small polished pieces and attacked for 3 hours in a 800 ml solution of 1N (NaOH + NA 2 CO 3 ) at 97 0 C. The results show that the presence of ZrO 2 in the glass composition increases its chemical durability to alkaline attack. Glasses of the aluminium/zirconium silicate series were melted with and without TiO 2 . It was shown experimentally that for this series of glasses, the presence of both TiO 2 and ZrO 2 gave better chemical durability results. However, the best overall results were obtained from the simpler zirconium silicate glasses, where it was possible to make glasses with higher values of ZrO 2 . (Author) [pt

Recycling of waste printed circuit boards with simultaneous enrichment of special metals by using alkaline melts: A green and strategically advantageous solution

Energy Technology Data Exchange (ETDEWEB)

Stuhlpfarrer, Philipp, E-mail: philipp-johannes.stuhlpfarrer@stud.unileoben.ac.at; Luidold, Stefan; Antrekowitsch, Helmut

2016-04-15

Highlights: • Removal of plastics. • Enrichment of In, Ga and Ge. • Low temperature. • No dioxines. - Abstract: The increasing consumption of electric and electronic equipment has led to a rise in toxic waste. To recover the metal fraction, a separation of the organic components is necessary because harmful substances such as chlorine, fluorine and bromine cause ecological damage, for example in the form of dioxins and furans at temperature above 400 °C. Hence, an alternative, environmentally friendly approach was investigated exploiting that a mixture of caustic soda and potassium hydroxide in eutectic composition melts below 200 °C, enabling a fast cracking of the long hydrocarbon chains. The trials demonstrate the removal of organic compounds without a loss of copper and precious metals, as well as a suppressed formation of hazardous off-gases. In order to avoid an input of alkaline elements into the furnace and ensuing problems with refractory materials, a washing step generates a sodium and potassium hydroxide solution, in which special metals like indium, gallium and germanium are enriched. Their concentrations facilitate the recovery of these elements, because otherwise they become lost in the typical recycling processes. The aim of this work was to find an environmental solution for the separation of plastics and metals as well as a strategically important answer for the recycling of printed circuit boards and mobile phones.

Recycling of waste printed circuit boards with simultaneous enrichment of special metals by using alkaline melts: A green and strategically advantageous solution.

Science.gov (United States)

Stuhlpfarrer, Philipp; Luidold, Stefan; Antrekowitsch, Helmut

2016-04-15

The increasing consumption of electric and electronic equipment has led to a rise in toxic waste. To recover the metal fraction, a separation of the organic components is necessary because harmful substances such as chlorine, fluorine and bromine cause ecological damage, for example in the form of dioxins and furans at temperature above 400°C. Hence, an alternative, environmentally friendly approach was investigated exploiting that a mixture of caustic soda and potassium hydroxide in eutectic composition melts below 200°C, enabling a fast cracking of the long hydrocarbon chains. The trials demonstrate the removal of organic compounds without a loss of copper and precious metals, as well as a suppressed formation of hazardous off-gases. In order to avoid an input of alkaline elements into the furnace and ensuing problems with refractory materials, a washing step generates a sodium and potassium hydroxide solution, in which special metals like indium, gallium and germanium are enriched. Their concentrations facilitate the recovery of these elements, because otherwise they become lost in the typical recycling processes. The aim of this work was to find an environmental solution for the separation of plastics and metals as well as a strategically important answer for the recycling of printed circuit boards and mobile phones. Copyright © 2015 Elsevier B.V. All rights reserved.

Recycling of waste printed circuit boards with simultaneous enrichment of special metals by using alkaline melts: A green and strategically advantageous solution

International Nuclear Information System (INIS)

Stuhlpfarrer, Philipp; Luidold, Stefan; Antrekowitsch, Helmut

2016-01-01

Highlights: • Removal of plastics. • Enrichment of In, Ga and Ge. • Low temperature. • No dioxines. - Abstract: The increasing consumption of electric and electronic equipment has led to a rise in toxic waste. To recover the metal fraction, a separation of the organic components is necessary because harmful substances such as chlorine, fluorine and bromine cause ecological damage, for example in the form of dioxins and furans at temperature above 400 °C. Hence, an alternative, environmentally friendly approach was investigated exploiting that a mixture of caustic soda and potassium hydroxide in eutectic composition melts below 200 °C, enabling a fast cracking of the long hydrocarbon chains. The trials demonstrate the removal of organic compounds without a loss of copper and precious metals, as well as a suppressed formation of hazardous off-gases. In order to avoid an input of alkaline elements into the furnace and ensuing problems with refractory materials, a washing step generates a sodium and potassium hydroxide solution, in which special metals like indium, gallium and germanium are enriched. Their concentrations facilitate the recovery of these elements, because otherwise they become lost in the typical recycling processes. The aim of this work was to find an environmental solution for the separation of plastics and metals as well as a strategically important answer for the recycling of printed circuit boards and mobile phones.

Advanced alkaline water electrolysis

International Nuclear Information System (INIS)

Marini, Stefania; Salvi, Paolo; Nelli, Paolo; Pesenti, Rachele; Villa, Marco; Berrettoni, Mario; Zangari, Giovanni; Kiros, Yohannes

2012-01-01

A short review on the fundamental and technological issues relevant to water electrolysis in alkaline and proton exchange membrane (PEM) devices is given. Due to price and limited availability of the platinum group metal (PGM) catalysts they currently employ, PEM electrolyzers have scant possibilities of being employed in large-scale hydrogen production. The importance and recent advancements in the development of catalysts without PGMs are poised to benefit more the field of alkaline electrolysis rather than that of PEM devices. This paper presents our original data which demonstrate that an advanced alkaline electrolyzer with performances rivaling those of PEM electrolyzers can be made without PGM and with catalysts of high stability and durability. Studies on the advantages/limitations of electrolyzers with different architectures do show how a judicious application of pressure differentials in a recirculating electrolyte scheme helps reduce mass transport limitations, increasing efficiency and power density.

Simulated bioavailability of phosphorus from aquatic macrophytes and hytoplankton by aqueous suspension and incubation with alkaline phosphatase

Science.gov (United States)

Bioavailability of phosphorus (P) in aquatic macrophytes and algae on lake eutrophication was studied by evaluation their P forms and quantities in their water suspensions and impact by alkaline phosphatase hydrolysis. using solution 31P-nuclear magnetic resonance (NMR). The laboratory suspension an...

The Influence of Mg(II and Ca(II Ions on Rutin Autoxidation in Weakly Alkaline Aqueous Solutions

Directory of Open Access Journals (Sweden)

Živanović Slavoljub C.

2016-09-01

Full Text Available Rutin (quercetin-3-O-rutinoside is one of the most abundant bioflavonoids with various biological and pharmacological activities. Considering the ubiquitous presence of Mg(II and Ca(II ions in biological systems we decided to investigate their influence on the autoxidation of rutin in weakly alkaline aqueous solutions. Changes in UV-Vis spectra recorded during the rutin autoxidation in aqueous solution at pH 8.4 revealed that this process was very slow in the absence of metal ions. The presence of Mg(II and, especially Ca(II ion, increased the transformation rate of rutin. UV-Vis spectra recorded after prolonged autoxidation indicated the formation of humic acidlike products in the presence of Mg(II and Ca(II ions. Four new compounds formed during the initial stage of rutin autoxidation in the presence of Mg(II and Ca(II ions were detected by HPLCDAD. Based on the analysis of their DAD UV-Vis spectra and comparison of their retention times with the retention time value for rutin, we concluded that the initial rutin transformation products were formed by the water addition on double bond in ring C and hydroxylation of ring B. A very small decrease of the initial rutin concentration (4% was observed by HPLC-DAD in the absence of metal ions for the period of 90 minutes. However, rutin concentration decrease was much larger in the presence of Mg(II and Ca(II ions (14% and 24%, respectively. The more pronounced effect of Ca(II ion on the rutin autoxidation may be explained by the stronger binding of Mg(II ion to rutin and thus greater stabilizing effect on reaction intermediates caused by its higher ionic potential (charge/ionic radius ratio in comparison to Ca(II ion. The results of this study may contribute to the better understanding of interactions of Mg(II and Ca(II ions with natural phenolic antioxidants which are important for their various biological activities.

Qualitative Carbohydrate Analysis using Alkaline Potassium ...

Indian Academy of Sciences (India)

IAS Admin

CLASSROOM. 285. RESONANCE | March 2016. Qualitative Carbohydrate Analysis using Alkaline. Potassium Ferricyanide. Keywords. Alkaline potassium ferricyanide, qualitative ... Carbohydrates form a distinct class of organic compounds often .... Laboratory Techniques: A contemporary Approach, W B Saunders Com-.

On an nth-order infinitesimal generator and time-dependent operator differential equation with a strongly almost periodic solution

Directory of Open Access Journals (Sweden)

Aribindi Satyanarayan Rao

2002-01-01

Full Text Available In a Banach space, if u is a Stepanov almost periodic solution of a certain nth-order infinitesimal generator and time-dependent operator differential equation with a Stepanov almost periodic forcing function, then u,u′,…,u (n−2 are all strongly almost periodic and u (n−1 is weakly almost periodic.

Mode of corrosion monitoring by electrochemical measurements in alkaline water solutions at 310 degC using a new type of industrial probes with high radiation stability

International Nuclear Information System (INIS)

Beran, J.

1977-01-01

Application of the linear polarization method to Zr-alloys and low-alloy steel was successfully verified by autoclave tests in alkaline water solutions, pH=10.3 max. The new type of industrial probes for electrochemical measurements worked 5500 hours at temperatures within 250 and 310 degC. Contrary to usual practice, the corrosion rate was evaluated applying the criterion T/Rsub(p) instead of criterion 1/Rsub(p). A single calibration curve T/Rsub(p) versus corrosion rate, which is independent of test temperature, was introduced in this way. The probes, developed by SKODA-Works, Nuclear Power Construction Division for electrochemical measurements in nuclear reactor environment, do not contain organic compounds (for sealing, insulation etc.) in order to prevent radiation damage. (author)

Behavior of technetium in alkaline solution: Identification of non-pertechnetate species in high-level nuclear waste tanks at the Hanford reservation

International Nuclear Information System (INIS)

Lukens, Wayne W. Jr.; Shuh, David K.; Schroeder, Norman C.; Ashley, Kenneth R.

2003-01-01

Technetium is a long-lived (99Tc: 213,000 year half-life) fission product found in nuclear waste and is one of the important isotopes of environmental concern. The known chemistry of technetium suggests that it should be found as pertechnetate, TcO4-, in the extremely basic environment of the nuclear waste tanks at the Hanford site. However, other chemical forms of technetium are present in significant amounts in certain tanks, and these non-pertechnetate species complicate the treatment of the waste. The only spectroscopic characterization of these non-pertechnetate species is a series of X-ray absorption near edge structure (XANES) spectra of actual tank waste. To better understand the behavior of technetium under these conditions, we have investigated the reduction of pertechnetate in highly alkaline solution in the presence of compounds found in high-level waste. These results and the X-ray absorption fine structure (XAFS) spectra of these species are compared to the chemical behavior and XANES spectra of the actual non-pertechnetate species. The identity of the nonpertechnetate species is surprising

Increased river alkalinization in the Eastern U.S.

Science.gov (United States)

Kaushal, Sujay S; Likens, Gene E; Utz, Ryan M; Pace, Michael L; Grese, Melissa; Yepsen, Metthea

2013-09-17

The interaction between human activities and watershed geology is accelerating long-term changes in the carbon cycle of rivers. We evaluated changes in bicarbonate alkalinity, a product of chemical weathering, and tested for long-term trends at 97 sites in the eastern United States draining over 260,000 km(2). We observed statistically significant increasing trends in alkalinity at 62 of the 97 sites, while remaining sites exhibited no significant decreasing trends. Over 50% of study sites also had statistically significant increasing trends in concentrations of calcium (another product of chemical weathering) where data were available. River alkalinization rates were significantly related to watershed carbonate lithology, acid deposition, and topography. These three variables explained ~40% of variation in river alkalinization rates. The strongest predictor of river alkalinization rates was carbonate lithology. The most rapid rates of river alkalinization occurred at sites with highest inputs of acid deposition and highest elevation. The rise of alkalinity in many rivers throughout the Eastern U.S. suggests human-accelerated chemical weathering, in addition to previously documented impacts of mining and land use. Increased river alkalinization has major environmental implications including impacts on water hardness and salinization of drinking water, alterations of air-water exchange of CO2, coastal ocean acidification, and the influence of bicarbonate availability on primary production.

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

Science.gov (United States)

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

2017-12-01

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

Competitive solvent extraction of alkaline-earth cations into chloroform by lipophilic acyclic polyether dicarboxylic acids

International Nuclear Information System (INIS)

Kang, S.I.; Czech, A.; Czech, B.P.; Stewart, L.E.; Bartsch, R.A.

1985-01-01

Competitive solvent extraction of alkaline-earth cations from aqueous solutions into chloroform by a series of lipophilic acyclic polyether dicarboxylic acids is reported. The influence of polyether chain length and of terminal carboxylic acid group variation upon extraction selectivity and efficiency is assessed. In the competitive extraction of concentrated magnesium, calcium, strontium and barium chloride solutions, one complexing agent exhibits pronounced selectivity for barium with Ba 2+ /S 2+ = 50, Ba 2+ /Ca 2+ = 250, and no detectable Mg 2+ extraction. 20 references, 3 figures, 1 table

Effect of Low-Temperature Environment on Stress Corrosion Cracking Behavior of X80 Pipeline Steel in Simulated Alkaline Soil Solution

Science.gov (United States)

Xie, Fei; Wang, Dan; Wu, Ming; Yu, Chengxiang; Sun, Dongxu; Yang, Xu; Xu, Changhao

2018-04-01

The stress corrosion cracking (SCC) of X80 pipeline steel in simulated alkaline soil solution under different temperatures was investigated by slow-strain-rate testing, scanning electron microscopy and energy-dispersive spectroscopy. Results showed that the fracture was transgranular and brittle at 273 K to 278 K (0 °C to 5 °C), and the metal surface was dissolved by a large number of chloride ions. Furthermore, hydrogen embrittlement was caused by the hydrogen atom extended to the high-stress region. The fracture process was controlled by hydrogen-induced cracking, and SCC was highly sensitive at this stage. At 288 K to 298 K (15 °C to 25 °C), the fracture morphology was attributed to the mixed mode of ductile and brittle fractures, the fracture process was controlled by the mechanism of hydrogen-induced cracking and anodic dissolution, and the susceptibility to SCC decreased. When the temperature reached 308 K to 318 K (35 °C to 45 °C), the fracture was mainly intergranular and ductile, the fracture process was controlled by anodic dissolution, and SCC sensitivity was the smallest in this temperature range.

Identification and characterization of miRNAs and targets in flax (Linum usitatissimum) under saline, alkaline, and saline-alkaline stresses.

Science.gov (United States)

Yu, Ying; Wu, Guangwen; Yuan, Hongmei; Cheng, Lili; Zhao, Dongsheng; Huang, Wengong; Zhang, Shuquan; Zhang, Liguo; Chen, Hongyu; Zhang, Jian; Guan, Fengzhi

2016-05-27

MicroRNAs (miRNAs) play a critical role in responses to biotic and abiotic stress and have been characterized in a large number of plant species. Although flax (Linum usitatissimum L.) is one of the most important fiber and oil crops worldwide, no reports have been published describing flax miRNAs (Lus-miRNAs) induced in response to saline, alkaline, and saline-alkaline stresses. In this work, combined small RNA and degradome deep sequencing was used to analyze flax libraries constructed after alkaline-salt stress (AS2), neutral salt stress (NSS), alkaline stress (AS), and the non-stressed control (CK). From the CK, AS, AS2, and NSS libraries, a total of 118, 119, 122, and 120 known Lus-miRNAs and 233, 213, 211, and 212 novel Lus-miRNAs were isolated, respectively. After assessment of differential expression profiles, 17 known Lus-miRNAs and 36 novel Lus-miRNAs were selected and used to predict putative target genes. Gene ontology term enrichment analysis revealed target genes that were involved in responses to stimuli, including signaling and catalytic activity. Eight Lus-miRNAs were selected for analysis using qRT-PCR to confirm the accuracy and reliability of the miRNA-seq results. The qRT-PCR results showed that changes in stress-induced expression profiles of these miRNAs mirrored expression trends observed using miRNA-seq. Degradome sequencing and transcriptome profiling showed that expression of 29 miRNA-target pairs displayed inverse expression patterns under saline, alkaline, and saline-alkaline stresses. From the target prediction analysis, the miR398a-targeted gene codes for a copper/zinc superoxide dismutase, and the miR530 has been shown to explicitly target WRKY family transcription factors, which suggesting that these two micRNAs and their targets may significant involve in the saline, alkaline, and saline-alkaline stress response in flax. Identification and characterization of flax miRNAs, their target genes, functional annotations, and gene

Posttranslational heterogeneity of bone alkaline phosphatase in metabolic bone disease.

Science.gov (United States)

Langlois, M R; Delanghe, J R; Kaufman, J M; De Buyzere, M L; Van Hoecke, M J; Leroux-Roels, G G

1994-09-01

Bone alkaline phosphatase is a marker of osteoblast activity. In order to study the posttranscriptional modification (glycosylation) of bone alkaline phosphatase in bone disease, we investigated the relationship between mass and catalytic activity of bone alkaline phosphatase in patients with osteoporosis and hyperthyroidism. Serum bone alkaline phosphatase activity was measured after lectin precipitation using the Iso-ALP test kit. Mass concentration of bone alkaline phosphatase was determined with an immunoradiometric assay (Tandem-R Ostase). In general, serum bone alkaline phosphatase mass and activity concentration correlated well. The activity : mass ratio of bone alkaline phosphatase was low in hyperthyroidism. Activation energy of the reaction catalysed by bone alkaline phosphatase was high in osteoporosis and in hyperthyroidism. Experiments with neuraminidase digestion further demonstrated that the thermodynamic heterogeneity of bone alkaline phosphatase can be explained by a different glycosylation of the enzyme.

A novel solution to the Klein–Gordon equation in the presence of a strong rotating electric field

Directory of Open Access Journals (Sweden)

E. Raicher

2015-11-01

Full Text Available The Klein–Gordon equation in the presence of a strong electric field, taking the form of the Mathieu equation, is studied. A novel analytical solution is derived for particles whose asymptotic energy is much lower or much higher than the electromagnetic field amplitude. The condition for which the new solution recovers the familiar Volkov wavefunction naturally follows. When not satisfied, significant deviation from the Volkov wavefunction is demonstrated. The new condition is shown to differ by orders of magnitudes from the commonly used one. As this equation describes (neglecting spin effects the emission processes and the particle motion in Quantum Electrodynamics (QED cascades, our results suggest that the standard theoretical approach towards this phenomenon should be revised.

Steel corrosion resistance in model solutions and reinforced mortar containing wastes

NARCIS (Netherlands)

Koleva, D.A.; Van Breugel, K.

2012-01-01

This work reports on the corrosion resistance of steel in alkaline model solutions and in cement-based materials (mortar). The model solutions and the mortar specimens were Ordinary Portland Cement (OPC) based. Further, hereby discussed is the implementation of an eco-friendly approach of waste

Carbon-supported cobalt catalyst for hydrogen generation from alkaline sodium borohydride solution

Energy Technology Data Exchange (ETDEWEB)

Xu, Dongyan; Liu, Xinmin; Cao, Changqing; Guo, Qingjie [College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042 (China); Dai, Ping [College of Electromechanical Engineering, Qingdao University of Science and Technology, Qingdao 266061 (China)

2008-08-01

Low cost transition metal catalysts with high performance are attractive for the development of on-board hydrogen generation systems by catalytic hydrolysis of sodium borohydride (NaBH{sub 4}) in fuel cell fields. In this study, hydrogen production from alkaline NaBH{sub 4} via hydrolysis process over carbon-supported cobalt catalysts was studied. The catalytic activity of the supported cobalt catalyst was found to be highly dependent on the calcination temperatures. The hydrogen generation rate increases with calcination temperatures in the range of 200-400 C, but a high calcination temperature above 500 C led to markedly decreased activity. X-ray diffraction patterns reveal that the catalysts experience phase transition from amorphous Co-B to crystalline cobalt hydroxide with increase in calcination temperatures. The reaction performance is also dependent on the concentration of NaBH{sub 4}, and the hydrogen generation rate increases for lower NaBH{sub 4} concentrations and decreases after reaching a maximum at 10 wt.% of NaBH{sub 4}. (author)

Improved electrodes and gas impurity investigations on alkaline electrolysers

DEFF Research Database (Denmark)

Reissner, R.; Schiller, G.; Knoeri, T.

Alkaline water electrolysis for hydrogenproduction is a well-established techniquebut some technological issues regarding thecoupling of alkaline water electrolysis andRenewable Energy Sources (RES) remain tobe improved.......Alkaline water electrolysis for hydrogenproduction is a well-established techniquebut some technological issues regarding thecoupling of alkaline water electrolysis andRenewable Energy Sources (RES) remain tobe improved....

Inactivation of peroxidase, pectinesterase and alkaline phosphatase in polymers as a model for irradiation of dried foodstuffs

NARCIS (Netherlands)

Roozen, J.P.

1972-01-01

This thesis consists of a summary only of 6 refereed scientific papers published in Lebensmittel -Wissenschaft und -Technologie 3, 37-40 (1970); 4, 24-26, 93-96, 158-162, 196-200 (1971); 5, 128-131 (1972).

Aqueous solutions containing an enzyme (peroxidase, alkaline phosphatase,

Plutonium(IV) precipitates formed in alkaline media in the presence of various anions

Energy Technology Data Exchange (ETDEWEB)

Krot, N.N.; Shilov, V.P.; Yusov, A.B.; Tananaev, I.G.; Grigoriev, M.S.; Garnov, A.Yu.; Perminov, V.P.; Astafurova, L.N.

1998-09-01

The tendency of Pu(IV) to hydrolyze and form true solutions, colloid solutions, or insoluble precipitates has been known since the Manhattan Project. Since then, specific studies have been performed to examine in detail the equilibria of Pu(IV) hydrolytic reactions in various media. Great attention also has been paid to the preparation, structure, and properties of Pu(IV) polymers or colloids. These compounds found an important application in sol-gel technology for the preparation of nuclear fuel materials. A most important result of these works was the conclusion that Pu(IV) hydroxide, after some aging, consists of very small PuO{sub 2} crystallites and should therefore be considered to be Pu(IV) hydrous oxide. However, studies of the properties and behavior of solid Pu(IV) hydroxide in complex heterogeneous systems are rare. The primary goal of this investigation was to obtain data on the composition and properties of Pu(IV) hydrous oxide or other compounds formed in alkaline media under different conditions. Such information is important to understand Pu(IV) behavior and the forms of its existence in the Hanford Site alkaline tank waste sludge. This knowledge then may be applied in assessing plutonium criticality hazards in the storage, retrieval, and treatment of Hanford Site tank wastes as well as in understanding its contribution to the transuranic waste inventory (threshold at 100 nCi/g or about 5 {times} 10{sup {minus}6} M) of the separate solution and solid phases.

Plutonium(IV) precipitates formed in alkaline media in the presence of various anions

International Nuclear Information System (INIS)

Krot, N.N.; Shilov, V.P.; Yusov, A.B.; Tananaev, I.G.; Grigoriev, M.S.; Garnov, A.Yu.; Perminov, V.P.; Astafurova, L.N.

1998-09-01

The tendency of Pu(IV) to hydrolyze and form true solutions, colloid solutions, or insoluble precipitates has been known since the Manhattan Project. Since then, specific studies have been performed to examine in detail the equilibria of Pu(IV) hydrolytic reactions in various media. Great attention also has been paid to the preparation, structure, and properties of Pu(IV) polymers or colloids. These compounds found an important application in sol-gel technology for the preparation of nuclear fuel materials. A most important result of these works was the conclusion that Pu(IV) hydroxide, after some aging, consists of very small PuO 2 crystallites and should therefore be considered to be Pu(IV) hydrous oxide. However, studies of the properties and behavior of solid Pu(IV) hydroxide in complex heterogeneous systems are rare. The primary goal of this investigation was to obtain data on the composition and properties of Pu(IV) hydrous oxide or other compounds formed in alkaline media under different conditions. Such information is important to understand Pu(IV) behavior and the forms of its existence in the Hanford Site alkaline tank waste sludge. This knowledge then may be applied in assessing plutonium criticality hazards in the storage, retrieval, and treatment of Hanford Site tank wastes as well as in understanding its contribution to the transuranic waste inventory (threshold at 100 nCi/g or about 5 x 10 -6 M) of the separate solution and solid phases

FLEXURAL PROPERTIES OF ALKALINE TREATED SUGAR PALM FIBRE REINFORCED EPOXY COMPOSITES

Directory of Open Access Journals (Sweden)

D. Bachtiar

2010-06-01

Full Text Available A study of the effect of alkaline treatment on the flexural properties of sugar palm fibre reinforced epoxy composites is presented in this paper. The composites were reinforced with 10% weight fraction of the fibres. The fibres were treated using sodium hydroxide (NaOH with 0.25 M and 0.5 M concentration solution for 1 hour, 4 hours and 8 hours soaking time. The purpose of treating fibres with alkali was to enhance the interfacial bonding between matrix and fibre surfaces. The maximum flexural strength occurred at 0.25 M NaOH solution with 1 hour of soaking time, i.e 96.71 MPa, improving by 24.41% from untreated fibre composite. But, the maximum flexural modulus took place at 0.5 M NaOH solution with 4 hours soaking time, i.e. 6948 MPa, improving by 148% from untreated composite.

Kinetic study of methanol oxidation on Pt2Ru3/C catalyst in the alkaline media

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A. V. TRIPKOVIC

2007-11-01

Full Text Available The interaction of acridine orange (AO with double-stranded (ds The electrochemical oxidation of methanol in NaOH solution was examined on a thin film Pt2Ru3/C electrode. The XRD pattern revealed that the Pt2Ru3 alloy consisted of a solid solution of Ru in Pt and a small amount of Ru or a solid solution of Pt in Ru. It was shown that in alkaline solution, the difference in activity between Pt/C and Pt2Ru3/C is significantly smaller than in acid solution. It is proposed that the reaction follows a quasi bifunctional mechanism. The kinetic parameters indicated that the chemical reaction between adsorbed COad and OHad species could be the rate limiting step.

Critical experiments on an enriched uranium solution system containing periodically distributed strong thermal neutron absorbers

International Nuclear Information System (INIS)

Rothe, R.E.

1996-01-01

A series of 62 critical and critical approach experiments were performed to evaluate a possible novel means of storing large volumes of fissile solution in a critically safe configuration. This study is intended to increase safety and economy through use of such a system in commercial plants which handle fissionable materials in liquid form. The fissile solution's concentration may equal or slightly exceed the minimum-critical-volume concentration; and experiments were performed for high-enriched uranium solution. Results should be generally applicable in a wide variety of plant situations. The method is called the 'Poisoned Tube Tank' because strong neutron absorbers (neutron poisons) are placed inside periodically spaced stainless steel tubes which separate absorber material from solution, keeping the former free of contamination. Eight absorbers are investigated. Both square and triangular pitched lattice patterns are studied. Ancillary topics which closely model typical plant situations are also reported. They include the effect of removing small bundles of absorbers as might occur during inspections in a production plant. Not taking the tank out of service for these inspections would be an economic advantage. Another ancillary topic studies the effect of the presence of a significant volume of unpoisoned solution close to the Poisoned Tube Tank on the critical height. A summary of the experimental findings is that boron compounds were excellent absorbers, as expected. This was true for granular materials such as Gerstley Borate and Borax; but it was also true for the flexible solid composed of boron carbide and rubber, even though only thin sheets were used. Experiments with small bundles of absorbers intentionally removed reveal that quite reasonable tanks could be constructed that would allow a few tubes at a time to be removed from the tank for inspection without removing the tank from production service

Development of alkaline/surfactant/polymer (ASP flooding technology for recovery of Karazhanbas oil

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Birzhan Zhappasbaev

2016-03-01

Full Text Available The tertiary oil recovery methods like alkaline, surfactant and polymer (ASP flooding are very perspective in order to achieve the synergetic effect out of the different impacts which are caused by these chemicals, which affect oil and water filtration in the reservoir and increase oil recovery. In this communication, we consider the applicability of hydrophobically modified polyampholyte – poly(hexadecylaminocrotonatebetaine (PHDACB as ASP flooding agent for recovery of oil from Karazhanbas oilfield. As “polysoap”, the aqueous solution of PHDACB dissolved in aqueous KOH was used. This system combines the advantages of alkaline, surfactant and polymer and exhibits the synergistic effect. The laboratory results showed that the ASP flooding considerably increases the oil recovery in addition to water flooding. In perspective, the ASP flooding may substitute the steam injection and other thermal enhanced oil recovery (EOR technologies.

Alkaline ionic liquids applied in supported ionic liquid catalyst for selective hydrogenation of citral to citronellal

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Eero eSalminen

2014-02-01

Full Text Available The challenge in preparation of ionic liquids containing a strong alkaline anion is to identify a suitable cation which can tolerate the harsh conditions induced by the anion. In this study, a commercial quaternary ammonium compound (quat benzalkonium [ADBA] (alkyldimethylbenzylammonium was used as a cation in the synthesis of different alkaline ionic liquids. In fact, the precursor, benzalkonium chloride, is a mixture of alkyldimethylbenzylammonium chlorides of various alkyl chain lengths and is commonly used in the formulation of various antiseptic products. The prepared ionic liquids were utilized as Supported Ionic Liquid Catalysts (SILCAs. Typically, a SILCA contains metal nanoparticles, enzymes or metal complexes in an ionic liquid layer which is immobilized on a solid carrier material such as an active carbon cloth (ACC. The catalysts were applied in the selective hydrogenation of citral to citronellal which is an important perfumery chemical. Interestingly, 70 % molar yield towards citronellal was achieved over a catalyst containing the alkaline ionic liquid benzalkonium methoxide.

Alkaline ionic liquids applied in supported ionic liquid catalyst for selective hydrogenation of citral to citronellal

Science.gov (United States)

Salminen, Eero; Virtanen, Pasi; Mikkola, Jyri-Pekka

2014-01-01

The challenge in preparation of ionic liquids containing a strong alkaline anion is to identify a suitable cation which can tolerate the harsh conditions induced by the anion. In this study, a commercial quaternary ammonium compound (quat) benzalkonium [ADBA] (alkyldimethylbenzylammonium) was used as a cation in the synthesis of different alkaline ionic liquids. In fact, the precursor, benzalkonium chloride, is a mixture of alkyldimethylbenzylammonium chlorides of various alkyl chain lengths and is commonly used in the formulation of various antiseptic products. The prepared ionic liquids were utilized as Supported Ionic Liquid Catalysts (SILCAs). Typically, a SILCA contains metal nanoparticles, enzymes, or metal complexes in an ionic liquid layer which is immobilized on a solid carrier material such as an active carbon cloth (ACC). The catalysts were applied in the selective hydrogenation of citral to citronellal which is an important perfumery chemical. Interestingly, 70% molar yield toward citronellal was achieved over a catalyst containing the alkaline ionic liquid benzalkonium methoxide. PMID:24790972

Application of alkaline solid residue of electric arc furnace dust for neutralization/purification of electroplating wastewaters.

Science.gov (United States)

Elez, Loris; Orescanin, Visnja; Sofilic, Tahir; Mikulic, Nenad; Ruk, Damir

2008-10-01

The purpose of this work was development of an appropriate procedure for the neutralization/purification of electroplating wastewater (EWW) with alkaline solid residue (ASR) by-product of the alkaline extraction of zinc and lead from electric arc furnace dust (EAFD). Removal efficiency of ASR at optimum purification conditions (pH 8 and mixing time; 20 minutes) for the elements Pb, Cr (VI), Cr (III), Fe, Ni, Cu and Zn were 94.92%, 97.58%, 99.59%, 99.48%, 97.25% and 99.97%, respectively. The concentrations of all elements in the purified wastewater were significantly lower in relation to the upper permissible limit for wastewaters suitable for discharge into the environment. The remaining waste mud was regenerated in the strong alkaline medium and successfully applied once again for the neutralization/purification of EWW. Removal efficiencies of heavy metals accomplished with regenerated waste mud were comparable to these achieved by original ASR. Elemental concentrations in the leachates of the waste mud were in accordance with regulated values.

Alkaline phosphatase binds tenaciously to titanium; implications for biological surface evaluation following bone implant retrieval.

Science.gov (United States)

Mansell, J P; Shiel, A I; Harwood, C; Stephens, D

2017-07-01

Enhancing the performance and longevity of titanium (Ti) implants continues to be a significant developmental theme in contemporary biomaterials design. Our specific focus pertains to the surface functionalisation of Ti using the bioactive lipid, lysophosphatidic acid (LPA) and certain phosphatase-resistant analogues of LPA. Coating survivorship to a plethora of testing regimens is required to align with due regulatory process before novel biomaterials can enter clinical trials. One of the key acceptance criteria is coating retention to the physical stresses experienced during implantation. In assessing coating stability to insertion into porcine bone we found that a subsequent in vitro assessment to confirm coating persistence was masked by abundant alkaline phosphatase (ALP) contamination adsorbed to the metal surface. Herein we report that ALP can bind to Ti in a matter of minutes by simply immersing Ti samples in aqueous solutions of the enzyme. We strongly discourage the in vitro monitoring of osteoblast and stromal cell ALP expression when assessing bioactive coating survivorship following Ti implant retrieval form native bone tissue. Copyright © 2017 Elsevier B.V. All rights reserved.

Strong solutions to a Navier–Stokes–Lamé system on a domain with a non-flat boundary

International Nuclear Information System (INIS)

Kukavica, Igor; Ziane, Mohammed; Tuffaha, Amjad

2011-01-01

In this paper, we consider a Navier–Stokes–Lamé system modeling a fluid–structure interaction. For a general domain, we establish local well-posedness for strong solutions in which initial velocity u 0 belongs to H 1 while the initial data (w 0 , w 1 ) for the elasticity equation belongs to (H 3/2+k , H 1/2+k ) for any k in (0, k 0 ) where k 0 is an explicit positive constant

Application of electrochemically generated ozone to the discoloration and degradation of solutions containing the dye Reactive Orange 122

International Nuclear Information System (INIS)

Santana, Mario H.P.; Da Silva, Leonardo M.; Freitas, Admildo C.; Boodts, Julien F.C.; Fernandes, Karla C.; De Faria, Luiz A.

2009-01-01

Aqueous solutions containing the commercial azo dye Reactive Orange 122 (RO122) were ozonated in acid and alkaline conditions. Ozone was electrochemically generated using a laboratory-made electrochemical reactor and applied using semi-batch conditions and a column bubble reactor. A constant ozone application rate of 0.25 g h -1 was used throughout. Color removal and degradation efficiency were evaluated as function of ozonation time, pH and initial dye concentration by means of discoloration kinetics and COD-TOC removal. Experimental findings revealed that pH affects both discoloration kinetics and COD-TOC removal. A single pseudo-first-order kinetic rate constant, k obs , for discoloration was found for ozonation carried out in alkaline solutions, contrary to acidic solutions where k obs depends on ozonation time. COD-TOC removal supports degradation of RO122 is more pronounced for alkaline conditions. Evaluation of the oxidation feasibility by means of the COD/TOC ratio indicates that the ozonation process in both acid and alkaline conditions leads to a reduction in recalcitrance of the soluble organic matter

Application of Raw and Alkaline-modified Coconut Shaft as a Biosorbent for Pb2+ Removal

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Edwin Andrew Ofudje

2015-04-01

Full Text Available The sorption capacity of untreated and alkaline-treated coconut shaft biosorbents for the removal of Pb2+ from aqueous solution was investigated in batch experiments. Effects of contact time, biosorbent dose, initial metal concentration, and pH on the sorption capacity were investigated. Optimum Pb2+ removal of 17.6 and 22.1 mg/g by untreated and alkaline-treated biomass was achieved at an initial metal concentration of 150 mg/L, a biomass dose of 0.7 g, a contact time of 80 min, and a pH of 4.0. The sorption data fitted well into the Langmuir isotherm, while kinetic modeling of the data from untreated biomass indicated conformity with the Lagergren pseudo-first-order model, whereas data from the treated biomass fit well with the Elovich model. FT-IR results gave indications of possible functional groups on the cell walls of the coconut shaft, including alcohols, amines, carboxylic acids, ester, and ethers. Thus, alkaline treatment of the coconut shafts enhanced the biosorption ability of Pb2+ onto the coconut shaft biomass.

Technetium behavior in sulfide and ferrous iron solutions

International Nuclear Information System (INIS)

Lee, S.Y.; Bondietti, E.A.

1982-01-01

Pertechnetate oxyanion ( 99 TcO 4- ), a potentially mobile species in leachate from a breached radioactive waste repository, was removed from a brine solution by precipitation with sulfide, iron, and ferrous sulfide at environmental pH's. Maghemite (ν-Fe 2 O 3 ) and geothite (α-FeOOH) were the dominant minerals in the precipitate obtained from the TcO 4- -ferrous iron reaction. The observation of small particle size and poor crystallinity of the minerals formed in the presence of Tc suggested that the Tc was incorporated into the mineral structure after reduction to a lower valence state. Amorphous ferrous sulfide, an initial phase precipitating in the TcO 4- -ferrous iron-sulfide reaction, was transformed to goethite and hematite (α-Fe 2 O 3 ) on aging. The black precipitate obtained from the TcO 4- -sulfide reaction was poorly crystallized technetium sulfide (Tc 2 S 7 ) which was insoluble in both acid and alkaline solution in the absence of strong oxidents. The results suggested that ferrous- and/or sulfide-bearing groundwaters and minerals in host rocks or backfill barriers could reduce the mobility of Tc through the formation of less-soluble Tc-bearing iron and/or sulfide minerals

Electrocatalytic Performance of Carbon Supported WO3-Containing Pd–W Nanoalloys for Oxygen Reduction Reaction in Alkaline Media

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Nan Cui

2018-05-01

Full Text Available In this paper, we report that WOx containing nanoalloys exhibit stable electrocatalytic performance in alkaline media, though bulk WO3 is easy to dissolve in NaOH solution. Carbon supported oxide-rich Pd–W alloy nanoparticles (PdW/C with different Pd:W atom ratios were prepared by the reduction–oxidation method. Among the catalysts, the oxide-rich Pd0.8W0.2/C (Pd/W = 8:2, atom ratio exhibits the highest catalytic activity for the oxygen reduction reaction. The X-ray photoelectron spectroscopy data shows that ~40% of Pd atoms and ~60% of the W atoms are in their oxide form. The Pd 3d5/2 binding energy of the oxide-rich Pd–W nanoalloys is higher than that of Pd/C, indicating the electronic structure of Pd is affected by the strong interaction between Pd and W/WO3. Compare to Pd/C, the onset potential of the oxygen reduction reaction at the oxide-rich Pd0.8W0.2/C shifts to a higher potential. The current density (mA·mg Pd−1 at the oxide-rich Pd0.8W0.2/C is ~1.6 times of that at Pd/C. The oxide-rich Pd0.8W0.2/C also exhibits higher catalytic stability than Pd/C, which demonstrates that it is a prospective candidate for the cathode of fuel cells operating with alkaline electrolyte.

Alkaline sorbent injection for mercury control

Science.gov (United States)

Madden, Deborah A.; Holmes, Michael J.

2002-01-01

A mercury removal system for removing mercury from combustion flue gases is provided in which alkaline sorbents at generally extremely low stoichiometric molar ratios of alkaline earth or an alkali metal to sulfur of less than 1.0 are injected into a power plant system at one or more locations to remove at least between about 40% and 60% of the mercury content from combustion flue gases. Small amounts of alkaline sorbents are injected into the flue gas stream at a relatively low rate. A particulate filter is used to remove mercury-containing particles downstream of each injection point used in the power plant system.

Increased liver alkaline phosphatase and aminotransferase ...

African Journals Online (AJOL)

The effect of daily, oral administration of ethanolic extract of Khaya senegalensis stem bark (2mg/kg body weight) for 18days on the alkaline phosphatase, aspartate and alanine aminotransferase activities of rat liver and serum were investigated. Compared with the control, the activities of liver alkaline phosphatase (ALP), ...

Interaction of calcium silicate hydrates (C-S-H), the main components of cement, with alkaline chlorides, analogy with clays

International Nuclear Information System (INIS)

Viallis-Terrisse, H.

2000-01-01

This work, belonging to a more general study on the structure and reactivity of cement, deals with the experimental and theoretical analysis of the interaction of alkaline chlorides with calcium silicate hydrates (C-S-H), the main components of cement paste. The interaction of alkaline cations with C-S-H is interfacial, involving both electrostatic and surface complexation mechanisms. The C-S-H surface is constituted of silanol sites, partially dissociated due to the high pH of the interstitial solution. The calcium ions, present in large amounts in the equilibrium solution of C-S-H, constitute potential determining ions for the C-S-H surface. The alkaline ions seem to compete with calcium for the same surface sites. The adsorption isotherms show that caesium presents a better affinity than sodium and lithium for the C-S-H surface. Moreover, solid-state NMR suggests that caesium forms with the surface sites inner-sphere complexes, whereas sodium seems to keep its hydration sphere. These results are in agreement with zeta potential measurements, which let suppose a specific adsorption of caesium ions, and an indifferent behaviour of both other alkaline ions. A model for the C-S-H surface was proposed, from the electric double layer model, and mass action laws expressing the complexation of the different ionic species with the silanol sites. The whole study relies on a structural analogy with smectites, some clays presenting well-known cationic adsorption properties. The structural similarity between both minerals is enhanced by some similarities of reactivity, though significant behaviour differences could also be noted. (author)

The effect of irrigated rice cropping on the alkalinity of two alkaline rice soils in the Sahel

NARCIS (Netherlands)

Asten, van P.J.A.; Zelfde, van 't J.A.; Zee, van der S.E.A.T.M.; Hammecker, C.

2004-01-01

Irrigated rice cropping is practiced to reclaim alkaline-sodic soils in many parts of the world. This practice is in apparent contrast with earlier studies in the Sahel, which suggests that irrigated rice cropping may lead to the formation of alkaline-sodic soils. Soil column experiments were done

Separating hydrogen and oxygen evolution in alkaline water electrolysis using nickel hydroxide

Science.gov (United States)

Chen, Long; Dong, Xiaoli; Wang, Yonggang; Xia, Yongyao

2016-01-01

Low-cost alkaline water electrolysis has been considered a sustainable approach to producing hydrogen using renewable energy inputs, but preventing hydrogen/oxygen mixing and efficiently using the instable renewable energy are challenging. Here, using nickel hydroxide as a redox mediator, we decouple the hydrogen and oxygen production in alkaline water electrolysis, which overcomes the gas-mixing issue and may increase the use of renewable energy. In this architecture, the hydrogen production occurs at the cathode by water reduction, and the anodic Ni(OH)2 is simultaneously oxidized into NiOOH. The subsequent oxygen production involves a cathodic NiOOH reduction (NiOOH→Ni(OH)2) and an anodic OH− oxidization. Alternatively, the NiOOH formed during hydrogen production can be coupled with a zinc anode to form a NiOOH-Zn battery, and its discharge product (that is, Ni(OH)2) can be used to produce hydrogen again. This architecture brings a potential solution to facilitate renewables-to-hydrogen conversion. PMID:27199009

Solution of the Eliashberg equations for a very strong electron-phonon coupling with a low-energy cutoff

International Nuclear Information System (INIS)

Weger, M.; Barbiellini, B.; Jarlborg, T.; Peter, M.; Santi, G.

1995-01-01

We solve the Eliashberg equations for the case of an explicit vector k dependence of the interactions, and of the resulting self-energies Σ 1 ( vector k,ω), Σ 2 ( vector k,ω). We consider a strong energy-dependence of the electron-electron scattering-rate τ ee -1 , which is associated with a strong energy-dependence of the electron-phonon matrix element g(k,k'). We characterize this energy-dependence by a cutoff ξ 1 , which is of the order of the phonon frequency ω ph . We find that we can account for a large number of unexpected features of the superconductivity of the cuprates by the BCS electron-phonon theory, if we consider very large values of the McMillan coupling constant λ ph , and small values of the cutoff ξ 1 . Specifically, the Coulomb interaction is found not to depress T c ; the isotope effect is strongly reduced when ξ 1 ph . We find solutions in which the gap function Δ( vector k,ω) has extended s-wave symmetry but is very anisotropic. We suggest that the underlying cause of the strong energy-dependence is a very small electronic screening parameter at the Fermi surface; the electron-phonon matrix element g is abnormally large, and this accounts for the high transition temperatures of the cuprates. An order of magnitude estimate suggests that the electron-phonon mechanism can account for transition temperatures up to about 200 K. We thus propose a very-strong-coupling theory, in which the renormalization functions, in particular the energy-renormalization X, depend very strongly on the superconducting gap Δ, and thus display a very strong temperature-dependence between T c and T=0. An experimental manifestation of the very strong coupling with a small cutoff is a zero bias anomaly sometimes observed in tunneling experiments. (orig.)

Catalytic oxidation of soot over alkaline niobates

International Nuclear Information System (INIS)

Pecchi, G.; Cabrera, B.; Buljan, A.; Delgado, E.J.; Gordon, A.L.; Jimenez, R.

2013-01-01

Highlights: ► No previous reported studies about alkaline niobates as catalysts for soot oxidation. ► NaNbO 3 and KNbO 3 perovskite-type oxides show lower activation energy than other lanthanoid perovskite-type oxides. ► The alkaline niobate does not show deactivation by metal loss. - Abstract: The lack of studies in the current literature about the assessment of alkaline niobates as catalysts for soot oxidation has motivated this research. In this study, the synthesis, characterization and assessment of alkaline metal niobates as catalysts for soot combustion are reported. The solids MNbO 3 (M = Li, Na, K, Rb) are synthesized by a citrate method, calcined at 450 °C, 550 °C, 650 °C, 750 °C, and characterized by AAS, N 2 adsorption, XRD, O 2 -TPD, FTIR and SEM. All the alkaline niobates show catalytic activity for soot combustion, and the activity depends basically on the nature of the alkaline metal and the calcination temperature. The highest catalytic activity, expressed as the temperature at which combustion of carbon black occurs at the maximum rate, is shown by KNbO 3 calcined at 650 °C. At this calcination temperature, the catalytic activity follows an order dependent on the atomic number, namely: KNbO 3 > NaNbO 3 > LiNbO 3 . The RbNbO 3 solid do not follow this trend presumably due to the perovskite structure was not reached. The highest catalytic activity shown by of KNbO 3 , despite the lower apparent activation energy of NaNbO 3 , stress the importance of the metal nature and suggests the hypothesis that K + ions are the active sites for soot combustion. It must be pointed out that alkaline niobate subjected to consecutive soot combustion cycles does not show deactivation by metal loss, due to the stabilization of the alkaline metal inside the perovskite structure.

Three-dimensional iron, nitrogen-doped carbon foams as efficient electrocatalysts for oxygen reduction reaction in alkaline solution

International Nuclear Information System (INIS)

Ma, Yanjiao; Wang, Hui; Feng, Hanqing; Ji, Shan; Mao, Xuefeng; Wang, Rongfang

2014-01-01

Graphical abstract: Three-dimentional Fe, N-doped carbon foams prepared by two steps exhibited comparable catalytic activity for oxygen reduction reaction to commercial Pt/C due to the unique structure and the synergistic effect of Fe and N atoms. - Highlights: • Three-dimensional Fe, N-doped carbon foam (3D-CF) were prepared. • 3D-CF exhibits comparable catalytic activity to Pt/C for oxygen reduction reaction. • The enhanced activity of 3D-CF results of its unique structure. - Abstract: Three-dimensional (3D) Fe, N-doped carbon foams (3D-CF) as efficient cathode catalysts for the oxygen reduction reaction (ORR) in alkaline solution are reported. The 3D-CF exhibit interconnected hierarchical pore structure. In addition, Fe, N-doped carbon without porous strucuture (Fe-N-C) and 3D N-doped carbon without Fe (3D-CF’) are prepared to verify the electrocatalytic activity of 3D-CF. The electrocatalytic performance of as-prepared 3D-CF for ORR shows that the onset potential on 3D-CF electrode positively shifts about 41 mV than those of 3D-CF’ and Fe-N-C respectively. In addition, the onset potential on 3D-CF electrode for ORR is about 27 mV more negative than that on commercial Pt/C electrode. 3D-CF also show better methanol tolerance and durability than commercial Pt/C catalyst. These results show that to synthesize 3D hierarchical pores with high specific surface area is an efficient way to improve the ORR performance

Investigations Into the Nature of Alkaline Soluble, Non-Pertechnetate Technetium

Energy Technology Data Exchange (ETDEWEB)

Rapko, Brian M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Bryan, Samuel A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Chatterjee, Sayandev [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Edwards, Matthew K. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Levitskaia, Tatiana G. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Peterson, James M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Peterson, Reid A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Sinkov, Sergey I. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2013-11-01

This report summarizes work accomplished in fiscal year (FY) 2013, exploring the chemistry of a low-valence technetium(I) species, [Tc(CO)₃(H₂O)₃]⁺, a compound of interest due to its implication in the speciation of alkaline-soluble technetium in several Hanford tank waste supernatants. Various aspects of FY 2013’s work were sponsored both by Washington River Protection Solutions and the U.S. Department of Energy’s Office of River Protection; because of this commonality, both sponsors’ work is summarized in this report. There were three tasks in this FY 2013 study. The first task involved examining the speciation of [(CO)₃Tc(H₂O)₃]⁺ in alkaline solution by ⁹⁹Tc nuclear magnetic resonance spectroscopy. The second task involved the purchase and installation of a microcalorimeter suitable to study the binding affinity of [(CO)₃Tc(H₂O)₃]⁺ with various inorganic and organic compounds relevant to Hanford tank wastes, although the actual measure of such binding affinities is scheduled to occur in future FYs. The third task involved examining the chemical reactivity of [(CO)₃Tc(H₂O)₃]⁺ as relevant to the development of a [(CO)₃Tc(H₂O)₃]⁺ spectroelectrochemical sensor based on fluorescence spectroscopy.

Separation of strontium ions from other alkaline earth metal ions using masking reagent

International Nuclear Information System (INIS)

Komatsu, Y.

1996-01-01

Cs + and Sr 2+ have been well known as serious elements in high level radioactive waste. Separation of Cs + has already been successful when using an ion-exchange method from solution in the presence of other alkali metal ions. The separation of Sr 2+ is, however, not so easy by any known separation method such as solvent-extraction and ion-exchange methods. This is because Sr 2+ is in the middle of the selectivity series, which is Mg 2+ > Ca 2+ > Sr 2+ > Ba 2+ for the solvent-extraction method and Ba 2+ > Sr 2+ > Ca 2+ > Mg 2+ for the ion- exchange method. In the present study, separation of strontium from other alkaline earth metal ions was studied by a combined use of three types of separation methods at 298 K: the solvent-extraction method was applied for the first separation, in which thenoyltrifluoroacetone (TTA, extractant) and trioctylphosphine oxide ( TOPO, adduct forming ligand) were used for the organic phase of the system. The separation factors for each combination of four alkaline earth metal ions were determined by the values of the distribution ratio. The Mg 2+ was well separated from Sr 2+ by the TTA-TOPO system. However, the separation of the combinations of Ca 2+ -Sr 2+ and Sr 2+ -Ba 2+ was not complete by the above solvent-extraction system. The second separation method, an ion-exchange method was applied using dihydrogen tetratitanate hydrate fibers (H 2 Ti 4 O 9 nH 2 O) as an ion exchanger to separate Sr 2+ and Ba 2+ . The separation factors for each combination of four alkaline earth metal ions were calculated by the values of the distribution coefficients. Ba 2+ was well separated from Sr 2+ by the ion-exchange method. To separate Ca 2+ and Sr 2+ , however, a modified solvent-extraction method was finally used in which H 2 Ti 4 O 9 nH 2 O was used as a masking reagent of Sr 2+ . After the dihydrogen tetratitanate hydrate fibers were contacted with the aqueous solution containing Ca 2+ and Sr 2+ , the organic solution containing TTA and TOPO

Comparative Detection of Alkaline Protease Production in Exiguobacterium acetylicum

International Nuclear Information System (INIS)

Gomaa, O.M.; EI Shafey, H.M.

2009-01-01

Alkaline protease is one of the most important enzymes in industry, medicine, and research. In the present work, a comparative detection for alkaline protease activity was established for instant detection of enzyme activity. Eight different alkalophilic bacterial isolates were compared based on the clear zone they produced on skim milk agar. One strain gave an absolute clear zone in 16 hours and was used for alkaline protease detection. The result of Phenotypic identification using Biology Microlog 3 identified the isolate as Exiguobacterium acetylicum. The isolate under study showed slightly different characteristics from a known Exiguobacterium acetylicum strain. The isolate tolerated alkaline conditions up to ph 11, while good growth was evident at ph 7, the maximum alkaline protease activity was observed at ph 9 which reached up to 109.01 U/ml. The alkaline activity assay using alkaline protease enzyme assay were coordinating with those obtained by conductivity; there was a relevant decrease in conductivity at the maximum increase in enzyme activity, which proved the cell membrane conductivity has a close relation to alkaline protease production. This isolate has tolerated gamma radiation, the increase in dose (up to 4 Gy) gave wider clear zones in terms of diameter and this was relevant to the conductivity measurements

Investigation into formation of nanoparticles of tetravalent neptunium in slightly alkaline aqueous solution

International Nuclear Information System (INIS)

Husar, Richard

2015-01-01

Considering the worldwide growing discharge of minor actinides and the current need for geological disposal facilities for radioactive waste, this work provides a contribution to the safety case concerning Np transport if it would be released from deep repository sites and moving from alkaline cement conditions (near-field) to more neutral environmental conditions (far-field). The reducing conditions in a nuclear waste repository render neptunium tetravalent, which is assumed to be immobile in aqueous environment due to the low solubility solution of Np(IV). For tetravalent actinide nuclides, the most significant transport should occur via colloidal particles. This work demonstrates the formation of intrinsic neptunium dioxide nanocrystals and amorphous Np(IV) silica colloids under environmentally relevant conditions. The dissociation of the initial soluble Np(IV) complex (i.e. [Np(IV)(CO 3 ) 5 ] 6- ) induces the intrinsic formation of nanocrystalline NpO 2 in the solution phase. The resulting irregularly shaped nanocrystals with an average size of 4 nm exhibit a face-centered cubic (fcc), fluorite-type structure (space group Fm anti 3m). The NCs tend to agglomerate under ambient conditions due to the weakly charged hydrodynamic surface at neutral pH (zetapotential ζ ∝0 mV). The formation of micron-sized agglomerates, composed of nanocrystals of 2-5 nm in size, and the subsequent precipitation cause immobilization of the major amount of Np(IV) in the Np carbonate system. Agglomeration of NpO 2 nanocrystals in dependence on time was indicated by PCS and UV-vis absorption spectroscopy with the changes of baseline characteristics and absorption maximum at 742 nm. Hitherto, unknown polynuclear species as intermediate species of NpO 2 nanocrystal formation were isolated from solution and observed by HR-TEM. These polynuclear Np species appear as dimers, trimers and hexanuclear compounds in analogy with those reported for other actinides. Intrinsic formation of NpO 2

Optical properties of alkaline earth borate glasses

African Journals Online (AJOL)

user

... devices; radiation shields, surgical lasers and their glass ceramic counter ... Alkaline earth oxides improve glass forming capability while heavy metal ... reports on optical properties of MO-B2O3 glasses containing alkaline earth oxides.

Alkaline resistant ceramics; Alkalimotstaandskraftiga keramer

Energy Technology Data Exchange (ETDEWEB)

Westberg, Stig-Bjoern [Vattenfall Utveckling AB, Aelvkarleby (Sweden)

2001-02-01

Despite durability in several environments, ceramics and refractories can not endure alkaline environments at high temperature. An example of such an environment is when burning biofuel in modern heat and power plants in which the demand for increasing efficiency results in higher combustion temperatures and content of alkaline substances in the flue gas. Some experiences of these environments has been gained from such vastly different equipment as regenerator chambers in the glass industry and MHD-generators. The grains of a ceramic material are usually bonded together by a glassy phase which despite it frequently being a minor constituent render the materials properties and limits its use at elevated temperature. The damage is usually caused by alkaline containing low-melting phases and the decrease of the viscosity of the bonding glass phase which is caused by the alkaline. The surfaces which are exposed to the flue gas in a modern power plant are not only exposed to the high temperature but also a corroding and eroding, particle containing, gas flow of high velocity. The use of conventional refractory products is limited to 1300-1350 deg C. Higher strength and fracture toughness as well as durability against gases, slag and melts at temperatures exceeding 1700 deg C are expected of the materials of the future. Continuous transport of corrosive compounds to the surface and corrosion products from the surface as well as a suitable environment for the corrosion to occur in are prerequisites for extensive corrosion to come about. The highest corrosion rate is therefore found in a temperature interval between the dew point and the melting point of the alkaline-constituent containing compound. It is therefore important that the corrosion resistance is sufficient in the environment in which alkaline containing melts or slag may appear. In environments such as these, even under normal circumstances durable ceramics, such as alumina and silicon carbide, are attacked

Effect of zinc phosphate chemical conversion coating on corrosion behaviour of mild steel in alkaline medium: protection of rebars in reinforced concrete

International Nuclear Information System (INIS)

Simescu, Florica; Idrissi, Hassane

2008-01-01

We outline the ability of zinc phosphate coatings, obtained by chemical conversion, to protect mild steel rebars against localized corrosion, generated by chloride ions in alkaline media. The corrosion resistance of coated steel, in comparison with uncoated rebars and coated and uncoated steel rebars embedded in mortar, were evaluated by open-circuit potential, potentiodynamic polarization, cronoamperometry and electrochemical impedance spectroscopy. The coated surfaces were characterized by x-ray diffraction and scanning electron microscopy. First, coated mild steel rebars were studied in an alkaline solution with and without chloride simulating a concrete pore solution. The results showed that the slow dissolution of the coating generates hydroxyapatite Ca 10 (PO 4 ) 6 (OH) 2 . After a long immersion, the coating became dense and provided an effective corrosion resistance compared with the mild steel rebar. Secondly, the coated and uncoated steel rebars embedded in mortar and immersed in chloride solution showed no corrosion or deterioration of the coated steel. Corrosion rate is considerably lowered by this phosphate coating.

Effect of zinc phosphate chemical conversion coating on corrosion behaviour of mild steel in alkaline medium: protection of rebars in reinforced concrete

Directory of Open Access Journals (Sweden)

Florica Simescu and Hassane Idrissi

2008-01-01

Full Text Available We outline the ability of zinc phosphate coatings, obtained by chemical conversion, to protect mild steel rebars against localized corrosion, generated by chloride ions in alkaline media. The corrosion resistance of coated steel, in comparison with uncoated rebars and coated and uncoated steel rebars embedded in mortar, were evaluated by open-circuit potential, potentiodynamic polarization, cronoamperometry and electrochemical impedance spectroscopy. The coated surfaces were characterized by x-ray diffraction and scanning electron microscopy. First, coated mild steel rebars were studied in an alkaline solution with and without chloride simulating a concrete pore solution. The results showed that the slow dissolution of the coating generates hydroxyapatite Ca10(PO46(OH2. After a long immersion, the coating became dense and provided an effective corrosion resistance compared with the mild steel rebar. Secondly, the coated and uncoated steel rebars embedded in mortar and immersed in chloride solution showed no corrosion or deterioration of the coated steel. Corrosion rate is considerably lowered by this phosphate coating.

Structural characterization of chemical warfare agent degradation products in decontamination solutions with proton band-selective (1)H-(31)P NMR spectroscopy.

Science.gov (United States)

Koskela, Harri; Hakala, Ullastiina; Vanninen, Paula

2010-06-15

Decontamination solutions, which are usually composed of strong alkaline chemicals, are used for efficient detoxification of chemical warfare agents (CWAs). The analysis of CWA degradation products directly in decontamination solutions is challenging due to the nature of the matrix. Furthermore, occasionally an unforeseen degradation pathway can result in degradation products which could be eluded to in standard analyses. Here, we present the results of the application of proton band-selective (1)H-(31)P NMR spectroscopy, i.e., band-selective 1D (1)H-(31)P heteronuclear single quantum coherence (HSQC) and band-selective 2D (1)H-(31)P HSQC-total correlation spectroscopy (TOCSY), for ester side chain characterization of organophosphorus nerve agent degradation products in decontamination solutions. The viability of the approach is demonstrated with a test mixture of typical degradation products of nerve agents sarin, soman, and VX. The proton band-selective (1)H-(31)P NMR spectroscopy is also applied in characterization of unusual degradation products of VX in GDS 2000 solution.

Temperature Dependence of Mineral Solubility in Water. Part 2. Alkaline and Alkaline Earth Bromides

Science.gov (United States)

Krumgalz, B. S.

2018-03-01

Databases of alkaline and alkaline earth bromide solubilities in water at various temperatures were created using experimental data from publications over about the last two centuries. Statistical critical evaluation of the created databases was produced since there were enough independent data sources to justify such evaluation. The reliable experimental data were adequately described by polynomial expressions over various temperature ranges. Using the Pitzer approach for ionic activity and osmotic coefficients, the thermodynamic solubility products for the discussed bromide minerals have been calculated at various temperature intervals and also represented by polynomial expressions.

Recent studies of uranium and plutonium chemistry in alkaline radioactive waste solutions

International Nuclear Information System (INIS)

King, William D.; Wilmarth, William R.; Hobbs, David T.; Edwards, Thomas B.

2008-01-01

Solubility studies of uranium and plutonium in a caustic, radioactive Savannah River Site tank waste solution revealed the existence of uranium supersaturation in the as-received sample. Comparison of the results to predictions generated from previously published models for solubility in these waste types revealed that the U model poorly predicts solubility while Pu model predictions are quite consistent with experimental observations. Separate studies using simulated Savannah River Site evaporator feed solution revealed that the known formation of sodium aluminosilicate solids in waste evaporators can promote rapid precipitation of uranium from supersaturated solutions

Purification and characterization of an alkaline protease from Micrococcus sp. isolated from the South China Sea

Science.gov (United States)

Hou, Enling; Xia, Tao; Zhang, Zhaohui; Mao, Xiangzhao

2017-04-01

Protease is wildly used in various fields, such as food, medicine, washing, leather, cosmetics and other industrial fields. In this study, an alkaline protease secreted by Micrococcus NH54PC02 isolated from the South China Sea was purified and characterized. The growth curve and enzyme activity curve indicated that the cell reached a maximum concentration at the 30th hour and the enzyme activity reached the maximum value at the 36th hour. The protease was purified with 3 steps involving ammonium sulfate precipitation, ion-exchange chromatography and hydrophobic chromatography with 8.22-fold increase in specific activity and 23.68% increase in the recovery. The molecular mass of the protease was estimated to be 25 kDa by SDS-PAGE analysis. The optimum temperature and pH for the protease activity were 50°C and pH 10.0, respectively. The protease showed a strong stability in a wide range of pH values ranging from 6.0-11.0, and maintained 90% enzyme activity in strong alkaline environment with pH 11.0. Inhibitor trials indicated that the protease might be serine protease. But it also possessed the characteristic of metalloprotease as it could be strongly inhibited by EDTA and strongly stimulated by Mn2+. Evaluation of matrix-assisted laser desorption ionization/time-of-flight MS (MALDI-TOF-TOF/MS) showed that the protease might belong to the peptidase S8 family.

Preferential solvation, ion pairing, and dynamics of concentrated aqueous solutions of divalent metal nitrate salts

Science.gov (United States)

Yadav, Sushma; Chandra, Amalendu

2017-12-01

We have investigated the characteristics of preferential solvation of ions, structure of solvation shells, ion pairing, and dynamics of aqueous solutions of divalent alkaline-earth metal nitrate salts at varying concentration by means of molecular dynamics simulations. Hydration shell structures and the extent of preferential solvation of the metal and nitrate ions in the solutions are investigated through calculations of radial distribution functions, tetrahedral ordering, and also spatial distribution functions. The Mg2+ ions are found to form solvent separated ion-pairs while the Ca2+ and Sr2+ ions form contact ion pairs with the nitrate ions. These findings are further corroborated by excess coordination numbers calculated through Kirkwood-Buff G factors for different ion-ion and ion-water pairs. The ion-pairing propensity is found to be in the order of Mg(NO3) 2 lead to the presence of substantial dynamical heterogeneity in these solutions of strongly interacting ions. The current study helps us to understand the molecular details of hydration structure, ion pairing, and dynamics of water in the solvation shells and also of ion diffusion in aqueous solutions of divalent metal nitrate salts.

Structural characterisations and mechanistic investigations of the selective dissolution of americium by the ferricyanide ions in alkaline media. Application for the partitioning americium curium

International Nuclear Information System (INIS)

Fouchard, Sebastien

2000-01-01

Americium exhibits a high solubility form in basic media under oxidant conditions, unlike the other Transplutonium elements (TPE). This property can be used in the frame of High Level Liquid Waste (HLLW) treatment in order to extract preferentially the americium element, the main responsible of the long term radiotoxicity of the nuclear waste. This soluble compound can be obtained by addition of a concentrated basic solution of Fe(CN) 6 3- ions on Am(OH) 3 precipitates. This technique enables a rapid extraction of Am by the synthesis of this soluble form in alkaline solutions. Under these conditions, the other TPE remain in the solid state as trivalent hydroxide solids, strongly insoluble. In the case of dissolutions involving large amounts of Am(OH) 3 , the formation of the soluble complex is concomitant with the appearance of a reddish precipitate in the basic solution. Dissolution experiments which were carried out on this solid in NaOH/Fe(CN) 6 3- have demonstrated the dependency of the solubility equilibria with the media. Spectroscopic studies (UV Visible, XAS) on the precipitate have enabled the determination of the chemical structure and the oxidation state of the americium in the solid: Na 2 Am(V)O 2 (OH) 3 ,nH 2 O. Electrochemical studies on the americium solution have confirmed that the oxidation of Am(OH) 3 by the Fe(CN) 6 3- ions in basic media could only lead to the pentavalent form. A stoichiometric study carries out between a AmO 2 + ion and one Fe(CN) 6 3- ion and the spectroscopic characterisation of this reaction have demonstrated that the Fe(CN) 6 3- ion didn't remain as an un-complexed form in solution after the alkaline mixing. These results tend to prove that this dissolution of Am(OH) 3 is much more complex than a simple oxidation by the Fe(CN) 6 3- ions. The existence of molecular interactions between AmO 2 + and Fe(CN) 6 3- has been postulated and a mechanistic scheme has been proposed in order to explain the appearance of the soluble

Development of composite membranes of PVA-TEOS doped KOH for alkaline membrane fuel cell

International Nuclear Information System (INIS)

Haryadi,; Sugianto, D.; Ristopan, E.

2015-01-01

Anion exchange membranes (AEMs) play an important role in separating fuel and oxygen (or air) in the Alkaline Membrane Fuel Cells. Preparation of hybrid organic inorganic materials of Polyvinylalcohol (PVA) - Tetraethylorthosilicate (TEOS) composite membrane doped KOH for direct alcohol alkaline fuel cell application has been investigated. The sol-gel method has been used to prepare the composite membrane of PVA-TEOS through crosslinking step and catalyzed by concentrated of hydrochloric acid. The gel solution was cast on the membrane plastic plate to obtain membrane sheets. The dry membranes were then doped by immersing in various concentrations of KOH solutions for about 4 hours. Investigations of the cross-linking process and the presence of hydroxyl group were conducted by FTIR as shown for frequency at about 1600 cm −1 and 3300 cm −1 respectively. The degree of swelling in ethanol decreased as the KOH concentration for membrane soaking process increased. The ion exchange capacity (IEC) of the membrane was 0.25meq/g. This composite membranes display significant ionic conductivity of 3.23 x 10 −2 S/cm in deionized water at room temperature. In addition, the morphology observation by scanning electron microscope (SEM) of the membrane indicates that soaking process of membrane in KOH increased thermal resistant

Development of composite membranes of PVA-TEOS doped KOH for alkaline membrane fuel cell

Science.gov (United States)

Haryadi, Sugianto, D.; Ristopan, E.

2015-12-01

Anion exchange membranes (AEMs) play an important role in separating fuel and oxygen (or air) in the Alkaline Membrane Fuel Cells. Preparation of hybrid organic inorganic materials of Polyvinylalcohol (PVA) - Tetraethylorthosilicate (TEOS) composite membrane doped KOH for direct alcohol alkaline fuel cell application has been investigated. The sol-gel method has been used to prepare the composite membrane of PVA-TEOS through crosslinking step and catalyzed by concentrated of hydrochloric acid. The gel solution was cast on the membrane plastic plate to obtain membrane sheets. The dry membranes were then doped by immersing in various concentrations of KOH solutions for about 4 hours. Investigations of the cross-linking process and the presence of hydroxyl group were conducted by FTIR as shown for frequency at about 1600 cm-1 and 3300 cm-1 respectively. The degree of swelling in ethanol decreased as the KOH concentration for membrane soaking process increased. The ion exchange capacity (IEC) of the membrane was 0.25meq/g. This composite membranes display significant ionic conductivity of 3.23 x 10-2 S/cm in deionized water at room temperature. In addition, the morphology observation by scanning electron microscope (SEM) of the membrane indicates that soaking process of membrane in KOH increased thermal resistant.

Development of composite membranes of PVA-TEOS doped KOH for alkaline membrane fuel cell

Energy Technology Data Exchange (ETDEWEB)

Haryadi,, E-mail: haryadi@polban.ac.id; Sugianto, D.; Ristopan, E. [Department of Chemical Engineering, Politeknik Negeri Bandung Jl. Gegerkalong Hilir, Ds. Ciwaruga, Bandung West Java (Indonesia)

2015-12-29

Anion exchange membranes (AEMs) play an important role in separating fuel and oxygen (or air) in the Alkaline Membrane Fuel Cells. Preparation of hybrid organic inorganic materials of Polyvinylalcohol (PVA) - Tetraethylorthosilicate (TEOS) composite membrane doped KOH for direct alcohol alkaline fuel cell application has been investigated. The sol-gel method has been used to prepare the composite membrane of PVA-TEOS through crosslinking step and catalyzed by concentrated of hydrochloric acid. The gel solution was cast on the membrane plastic plate to obtain membrane sheets. The dry membranes were then doped by immersing in various concentrations of KOH solutions for about 4 hours. Investigations of the cross-linking process and the presence of hydroxyl group were conducted by FTIR as shown for frequency at about 1600 cm{sup −1} and 3300 cm{sup −1} respectively. The degree of swelling in ethanol decreased as the KOH concentration for membrane soaking process increased. The ion exchange capacity (IEC) of the membrane was 0.25meq/g. This composite membranes display significant ionic conductivity of 3.23 x 10{sup −2} S/cm in deionized water at room temperature. In addition, the morphology observation by scanning electron microscope (SEM) of the membrane indicates that soaking process of membrane in KOH increased thermal resistant.

Alkaline pretreatment of Mexican pine residues for bioethanol ...

African Journals Online (AJOL)

Alkaline pretreatment of Mexican pine residues for bioethanol production. ... Keywords: Lignocellulosic biomass, alkaline pretreatment, enzymatic hydrolysis, fermentable sugars, fermentation. African Journal of Biotechnology Vol. 12(31), pp.

Alkaline rocks and the occurrence of uranium

International Nuclear Information System (INIS)

Hambleton-Jones, B.B.; Toens, P.D.

1980-10-01

Many alkaline complexes contain uranium and other minerals in low concentrations and are regarded as constituting valuable potential reserves. Certain complex metallurgical problems, however, remain to be solved. Alkaline rocks occur in a number of forms and environments and it is noted that they are generated during periods of geological quiescence emplaced mainly in stable aseismic areas. Many occur along the extensions of oceanic transform faults beneath the continental crust and the application of this concept to areas not currently known to host alkaline complexes may prove useful in identifying potential target areas for prospecting operations [af

Effect of acid and alkaline solubilization on the properties of surimi based film

Directory of Open Access Journals (Sweden)

Thummanoon Prodpran

2005-05-01

Full Text Available The effect of acid and alkaline solubilizing processes on the properties of the protein based film from threadfin bream surimi was investigated. Surimi films prepared from both processes had the similar light transmission, tensile strength (TS and elongation at break (EAB (P<0.05. However, film with alkaline process had slightly lower water vapor permeability (WVP, compared to that prepared by acid solubilizing process. The protein concentration in the film-forming solution directly affected the properties of the film. Increase in protein concentration resulted in an increase in TS, EAB as well as WVP. The film prepared by acid solubilizing process had an increase in yellowish color as evidenced by the continuous increase in b* and E* values during the storage at r oom temperature. The acid and alkali solubilizing processes caused the degradation of muscle protein in surimi, especially with increasing exposure time. Therefore, solubilizing process had the influence on the properties of the protein film from threadfin bream surimi.

Power ultrasound irradiation during the alkaline etching process of the 2024 aluminum alloy

Energy Technology Data Exchange (ETDEWEB)

Moutarlier, V.; Viennet, R.; Rolet, J.; Gigandet, M.P.; Hihn, J.Y., E-mail: jean-yves.hihn@univ-fcomte.fr

2015-11-15

Graphical abstract: Result of an etching step in ultrasound presence on intermetallic particles on a 2024 aluminum alloy. - Highlights: • Etching step prior to anodization on 2024 aluminum alloy. • Etching rate measurement and hydroxide film characterization by GDOES and SEM. • Various etching parameters (temperature, presence or absence of ultrasound). • Improvement of corrosion resistance show by electrochemical tests. - Abstract: Prior to any surface treatment on an aluminum alloy, a surface preparation is necessary. This commonly consists in performing an alkaline etching followed by acid deoxidizing. In this work, the use of power ultrasound irradiation during the etching step on the 2024 aluminum alloy was studied. The etching rate was estimated by weight loss, and the alkaline film formed during the etching step was characterized by glow discharge optical emission spectrometry (GDOES) and scanning electron microscope (SEM). The benefit of power ultrasound during the etching step was confirmed by pitting potential measurement in NaCl solution after a post-treatment (anodizing).

Power ultrasound irradiation during the alkaline etching process of the 2024 aluminum alloy

International Nuclear Information System (INIS)

Moutarlier, V.; Viennet, R.; Rolet, J.; Gigandet, M.P.; Hihn, J.Y.

2015-01-01

Graphical abstract: Result of an etching step in ultrasound presence on intermetallic particles on a 2024 aluminum alloy. - Highlights: • Etching step prior to anodization on 2024 aluminum alloy. • Etching rate measurement and hydroxide film characterization by GDOES and SEM. • Various etching parameters (temperature, presence or absence of ultrasound). • Improvement of corrosion resistance show by electrochemical tests. - Abstract: Prior to any surface treatment on an aluminum alloy, a surface preparation is necessary. This commonly consists in performing an alkaline etching followed by acid deoxidizing. In this work, the use of power ultrasound irradiation during the etching step on the 2024 aluminum alloy was studied. The etching rate was estimated by weight loss, and the alkaline film formed during the etching step was characterized by glow discharge optical emission spectrometry (GDOES) and scanning electron microscope (SEM). The benefit of power ultrasound during the etching step was confirmed by pitting potential measurement in NaCl solution after a post-treatment (anodizing).

Preparation and Characterization of PVA Alkaline Solid Polymer Electrolyte with Addition of Bamboo Charcoal

OpenAIRE

Lidan Fan; Mengyue Wang; Zhen Zhang; Gang Qin; Xiaoyi Hu; Qiang Chen

2018-01-01

Natural bamboo charcoal (BC) powder has been developed as a novel filler in order to further improve performances of the polyvinyl alcohol (PVA)-based alkaline solid polymer electrolyte (ASPE) by solution casting method. X-ray diffraction patterns of composite polymer electrolyte with BC revealed the decrease in the degree of crystallinity with increasing content of BC. Scanning electron microscopy images showed pores on a micrometer scale (average diameter about 2 μm) distributed inside a...

Assessing ocean alkalinity for carbon sequestration

Science.gov (United States)

Renforth, Phil; Henderson, Gideon

2017-09-01

Over the coming century humanity may need to find reservoirs to store several trillions of tons of carbon dioxide (CO2) emitted from fossil fuel combustion, which would otherwise cause dangerous climate change if it were left in the atmosphere. Carbon storage in the ocean as bicarbonate ions (by increasing ocean alkalinity) has received very little attention. Yet recent work suggests sufficient capacity to sequester copious quantities of CO2. It may be possible to sequester hundreds of billions to trillions of tons of C without surpassing postindustrial average carbonate saturation states in the surface ocean. When globally distributed, the impact of elevated alkalinity is potentially small and may help ameliorate the effects of ocean acidification. However, the local impact around addition sites may be more acute but is specific to the mineral and technology. The alkalinity of the ocean increases naturally because of rock weathering in which >1.5 mol of carbon are removed from the atmosphere for every mole of magnesium or calcium dissolved from silicate minerals (e.g., wollastonite, olivine, and anorthite) and 0.5 mol for carbonate minerals (e.g., calcite and dolomite). These processes are responsible for naturally sequestering 0.5 billion tons of CO2 per year. Alkalinity is reduced in the ocean through carbonate mineral precipitation, which is almost exclusively formed from biological activity. Most of the previous work on the biological response to changes in carbonate chemistry have focused on acidifying conditions. More research is required to understand carbonate precipitation at elevated alkalinity to constrain the longevity of carbon storage. A range of technologies have been proposed to increase ocean alkalinity (accelerated weathering of limestone, enhanced weathering, electrochemical promoted weathering, and ocean liming), the cost of which may be comparable to alternative carbon sequestration proposals (e.g., $20-100 tCO2-1). There are still many

catalysed oxidation of atenolol by alkaline permanganate

Indian Academy of Sciences (India)

Unknown

Abstract. Kinetics of ruthenium (III) catalyzed oxidation of atenolol by permanganate in alkaline medium at constant ionic strength of 0⋅30 mol dm3 has been studied spectrophotometrically using a rapid kinetic accessory. Reaction between permanganate and atenolol in alkaline medium exhibits 1 : 8 stoichiometry.

Combined chemical and EIS study of the reaction of zinc coatings under alkaline conditions

International Nuclear Information System (INIS)

Walkner, Sarah; Hassel, Achim Walter

2014-01-01

Graphical abstract: - Highlights: • An electrochemical unit for automatic EIS and pH modulation is used. • ZnMg2Al2 and ZnAl53 are studied in alkaline solutions. • Amount of consumed sodium hydroxide allows following hydroxide formation and film thickness. • Cross sections of 13 μm show excellent agreement with consumed hydroxide. • ZnAl53 consumes more hydroxide due to soluble aluminate formation. - Abstract: Two different zinc coatings of composition ZnMg2Al2 (Zn + 2 wt.% Mg + 2 wt.% Al) and ZnAl53 (Zn + 53 wt.% Al) were investigated in aqueous solution at pH 12.0 with a novel setup, the so-called impedance titrator. This device is able to perform electrochemical measurements including, but not limited to, impedance spectroscopy in dependency of different pH-values. The setup allows holding the pH-value with a precision of at least 0.05 by dosing the required amount of titrating agent to the system. If the alkaline pH region is investigated, hydroxide ions are consumed in the course of passive layer formation. The amount of consumed hydroxide allows to quantitatively follow the formation of the hydroxide film and its thickness. Cross section SEM shows an excellent agreement of 13 μm after 7 h for ZnMg2Al2. At a constant pH value, the hydroxide concentration is constant and film formation is well defined and kinetically characterised. The consumption of hydroxide by the ZnAl53 coating is higher resulting from the solubility of the Al as aluminate under alkaline conditions. The composition of the precipitates contains less than 3 wt.% of Al. The observed processes and the formation of corrosion products are recorded and differences in the behaviour of the two coatings are discussed

Asymptotic behaviour of solutions of the first boundary-value problem for strongly hyperbolic systems near a conical point at the boundary of the domain

International Nuclear Information System (INIS)

Hung, Nguyen M

1999-01-01

An existence and uniqueness theorem for generalized solutions of the first initial-boundary-value problem for strongly hyperbolic systems in bounded domains is established. The question of estimates in Sobolev spaces of the derivatives with respect to time of the generalized solution is discussed. It is shown that the smoothness of generalized solutions with respect to time is independent of the structure of the boundary of the domain but depends on the coefficients of the right-hand side. Results on the smoothness of the generalized solution and its asymptotic behaviour in a neighbourhood of a conical boundary point are also obtained

Recovery of fission products from waste solutions utilizing controlled cathodic potential electrolysis

International Nuclear Information System (INIS)

Carlin, W.W.; Darlington, W.B.

1975-01-01

Fission products, e.g., palladium, rhodium and technetium, are recovered from aqueous waste solutions thereof, e.g., aged Purex alkaline waste solutions. The metal values from the waste solutions are extracted by ion exchange techniques. The metals adsorbed by the ion exchange resin are eluted and selectively recovered by controlled cathodic potential electrolysis. The metal values deposited on the cathode are recovered and, if desired, further purified

Formation of chemical gardens on granitic rock. A new type of alteration for alkaline systems

Energy Technology Data Exchange (ETDEWEB)

Satoh, Hisao [Mitsubishi Materials Corporation, Naka (Japan). Energy Project and Technology Center; Tsukamoto, Katsuo [Tohoku Univ. Aramaki, Sendai (Japan). Dept. of Earth and Planetary Materials Science; Garcia-Ruiz, Juan Manuel [Granada Univ., Armilla (Spain). Lab. de Estudios Cristalograficos

2014-06-15

In order to understand the groundwater flow at near-underground facilities such as waste repositories, we have studied the effects of flowing an alkaline solution leached from cementitious building materials through the fractures of low-porosity granitic rocks under laboratory conditions. The results show that silica released from the dissolution of sodium-rich plagioclase and quartz reacts with the calcium leached from cementitious buildings to form calcium silicate hydrates (C-S-H) phases in the form of hollow tubular structures. These tubular structures form selectively on the surface of plagioclase in a similar way to reverse silica gardens structures. It was found that the rate of precipitation of C-S-H phases is faster than the rate of dissolution of plagioclase. This selftriggered dissolution/precipitation phenomenon may be an important factor controlling groundwater permeation in natural alkaline underground systems.

Formation of chemical gardens on granitic rock. A new type of alteration for alkaline systems

International Nuclear Information System (INIS)

Satoh, Hisao; Tsukamoto, Katsuo; Garcia-Ruiz, Juan Manuel

2014-01-01

In order to understand the groundwater flow at near-underground facilities such as waste repositories, we have studied the effects of flowing an alkaline solution leached from cementitious building materials through the fractures of low-porosity granitic rocks under laboratory conditions. The results show that silica released from the dissolution of sodium-rich plagioclase and quartz reacts with the calcium leached from cementitious buildings to form calcium silicate hydrates (C-S-H) phases in the form of hollow tubular structures. These tubular structures form selectively on the surface of plagioclase in a similar way to reverse silica gardens structures. It was found that the rate of precipitation of C-S-H phases is faster than the rate of dissolution of plagioclase. This selftriggered dissolution/precipitation phenomenon may be an important factor controlling groundwater permeation in natural alkaline underground systems.

IUPAC-NIST Solubility Data Series. 95. Alkaline Earth Carbonates in Aqueous Systems. Part 2. Ca

Science.gov (United States)

Vanderdeelen, Jan

2012-06-01

The alkaline earth carbonates are an important class of minerals. This article is part of a volume in the IUPAC-NIST Solubility Data Series that compiles and critically evaluates solubility data of the alkaline earth carbonates in water and in simple aqueous electrolyte solutions. Part 1 outlined the procedure adopted in this volume, and presented the beryllium and magnesium carbonates. Part 2, the current paper, compiles and critically evaluates the solubility data of calcium carbonate. The chemical forms included are the anhydrous CaCO3 types calcite, aragonite, and vaterite, the monohydrate monohydrocalcite (CaCO3. H2O), the hexahydrate ikaite (CaCO3.6H2O), and an amorphous form. The data were analyzed with two model variants, and thermodynamic data of each form consistent with each of the models and with the CODATA key values for thermodynamics are presented.

Alkaline-earth metal bicarbonates as lixiviants for uranium (VI) under CO2 sparging

International Nuclear Information System (INIS)

Vaziri, F.; White, D.A.

1989-01-01

In recent years it has become apparent that uranium is significantly soluble in solutions of alkaline-earth metal bicarbonates -particularly those of magnesium and calcium. A system has been proposed by previous authors in which milled uranium ore is leached in a medium to which an oxidizing agent, the metal hydroxide and CO 2 are added. The alkaline-earth metal hydroxides are much more readily soluble in this medium than the corresponding carbonates. Magnesium and calcium bicarbonates are quite soluble in aqueous media at neutral or nearly neutral pH. The pH determines the relative quantities of bicarbonate and carbonate ions in the system. Even if the pH is quite low, small amounts of carbonate ion are present that can complex with the uranyl ion to produce anionic uranyl complexes. Both UO 2 (CO 3 ) 2 2- and UO 2 (CO 3 ) 3 4- complexes are known and both have a very high stability constant. Despite the appearance of several patents on the use of alkaline-earth metal ions in carbonate media as uranium lixiviants, little theoretical or experimental work on the system has been published. In view of the potential of these systems for cheap, large-scale dissolution of uranium the present contribution will discuss the theory behind this method and provide some experimental data to verify the theoretical treatment. (author)

Strong work-hardening behavior induced by the solid solution strengthening of dendrites in TiZr-based bulk metallic glass matrix composites

Energy Technology Data Exchange (ETDEWEB)

Ma, D.Q. [State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004 (China); Jiao, W.T. [College of Education, Hebei Normal University of Science and Technology, Qinhuangdao 066004 (China); Zhang, Y.F. [State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004 (China); Hebei Vocational and Technical College of Building Materials, Qinhuangdao 066004 (China); Wang, B.A.; Li, J.; Zhang, X.Y. [State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004 (China); Ma, M.Z., E-mail: mz550509@ysu.edu.cn [State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004 (China); Liu, R.P. [State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004 (China)

2015-03-05

Highlights: • Hardness of dendrite of TiZr-based BMGMCs increases. • Strong work-hardening behavior is obtained after solid solution strengthening. • Lattice distortions of dendrite suffering from rapid cooling are detected. - Abstract: A series of TiZr-based bulk metallic glass matrix composites (BMGMCs) with distinguished mechanical properties are successfully fabricated by adding different volume fractions of Ta (Ti{sub 38.8}Zr{sub 28.8}Cu{sub 6.2}Be{sub 16.2}Nb{sub 10} as the basic composition, denoted as Ta{sub 0.0}–Ta{sub 8.0}). Along with the growth of precipitated phase, typical dendritic morphology is fully developed in the TiZr-based BMGMCs of Ta{sub 8.0}. Energy-dispersive spectrometry analysis of the dendrites and glass matrix indicates that the metallic elements of Nb and Ta should preferentially form solid solution into dendrites. The chaotic structure of high-temperature precipitate phase is trapped down by the rapid cooling of the copper-mould. The detected lattice distortions in the dendrites are attributed to the strong solid solution strengthening of the metallic elements of Ti, Zr, Nb, and Ta. These lattice distortions increase the resistance of the dislocation motion and pin the dislocations, thus the strength and hardness of dendrite increase. Dendrites create a strong barrier for the shear band propagation and generate multiple shear bands after solid solution strengthening, thereby providing the TiZr-based BMGMCs with greatly improved capacity to sustain plastic deformation and resistance to brittle fracture. Thus, the TiZr-based BMGMCs possess distinguished work-hardening capability. Among these TiZr-based BMGMCs, the sample Ta{sub 0.5} possesses the largest plastic strain (ε{sub p}) at 20.3% and ultimate strength (σ{sub max}) of 2613 MPa during compressive loading. In addition, the sample of Ta{sub 0.5} exhibits work-hardening up to an ultrahigh tensile strength of 1680 MPa during the tensile process, and then progressively

Introducing catalyst in alkaline membrane for improved performance direct borohydride fuel cells

Science.gov (United States)

Qin, Haiying; Lin, Longxia; Chu, Wen; Jiang, Wei; He, Yan; Shi, Qiao; Deng, Yonghong; Ji, Zhenguo; Liu, Jiabin; Tao, Shanwen

2018-01-01

A catalytic material is introduced into the polymer matrix to prepare a novel polymeric alkaline electrolyte membrane (AEM) which simultaneously increases ionic conductivity, reduces the fuel cross-over. In this work, the hydroxide anion exchange membrane is mainly composed of poly(vinylalcohol) and alkaline exchange resin. CoCl2 is added into the poly(vinylalcohol) and alkaline exchange resin gel before casting the membrane to introduce catalytic materials. CoCl2 is converted into CoOOH after the reaction with KOH solution. The crystallinity of the polymer matrix decreases and the ionic conductivity of the composite membrane is notably improved by the introduction of Co-species. A direct borohydride fuel cell using the composite membrane exhibits an open circuit voltage of 1.11 V at 30 °C, which is notably higher than that of cells using other AEMs. The cell using the composite membrane achieves a maximum power density of 283 mW cm-2 at 60 °C while the cell using the membrane without Co-species only reaches 117 mW cm-2 at the same conditions. The outstanding performance of the cell using the composite membrane benefits from impregnation of the catalytic Co-species in the membrane, which not only increases the ionic conductivity but also reduces electrode polarization thus improves the fuel cell performance. This work provides a new approach to develop high-performance fuel cells through adding catalysts in the electrolyte membrane.

Alkaline Leaching of Key, Non-Radioactive Components from Simulants and Hanford Tank Sludge 241-S-110: Results of FY01 Studies

Energy Technology Data Exchange (ETDEWEB)

Rapko, Brian M.; Vienna, John D.; Sinkov, Serguei I.; Kim, Jinseong; Cisar, Alan J.

2002-09-10

This study addressed three aspects in selected alkaline leaching: first, the use of oxidants persulfate, permanganate, and ferrate as selective chromium-leaching agents from washed Hanford Tank S-110 solids under varying conditions of hydroxide concentration, temperature, and time was investigated. Second, the selective dissolution of solids containing mercury(II) oxide under alkaline conditions was examined. Various compounds were studied for their effectiveness in dissolving mercury under varying conditions of time, temperature, and hydroxide concentration in the leachate. Three compounds were studied: cysteine, iodide, and diethyldithiophosphoric acid (DEDTPA). Finally, the possibility of whether an oxidant bound to an anion-exchange resin can be used to effectively oxidize chromium(III) in alkaline solutions was addressed. The experimental results remain ambiguous to date; further work is required to reach any definitive conclusions as to the effectiveness of this approach.

Alkaline batteries for hybrid and electric vehicles

Science.gov (United States)

Haschka, F.; Warthmann, W.; Benczúr-Ürmössy, G.

Forced by the USABC PNGV Program and the EZEV regulation in California, the development of hybrid vehicles become more strong. Hybrids offer flexible and unrestricted mobility, as well as pollution-free driving mode in the city. To achieve these requirements, high-power storage systems are demanded fulfilled by alkaline batteries (e.g., nickel/cadmium, nickel/metal hydride). DAUG has developed nickel/cadmium- and nickel/metal hydride cells in Fibre Technology of different performance types (up to 700 W/kg peak power) and proved in electric vehicles of different projects. A special bipolar cell design will meet even extreme high power requirements with more than 1000 W/kg peak power. The cells make use of the Recom design ensuring high power charge ability at low internal gas pressure. The paper presents laboratory test results of cells and batteries.

Alkaline batteries for hybrid and electric vehicles

Energy Technology Data Exchange (ETDEWEB)

Haschka, F.; Warthmann, W.; Benczur-Uermoessy, G. [DAUG Deutsche Automobilgesellschaft, Esslingen (Germany)

1998-03-30

Forced by the USABC PNGV Program and the EZEV regulation in California, the development of hybrid vehicles become more strong. Hybrids offer flexible and unrestricted mobility, as well as pollution-free driving mode in the city. To achieve these requirements, high-power storage systems are demanded fulfilled by alkaline batteries (e.g. nickel/cadmium, nickel/metal hydride). DAUG has developed nickel/cadmium- and nickel/metal hydride cells in Fibre Technology of different performance types (up to 700 W/kg peak power) and proved in electric vehicles of different projects. A special bipolar cell design will meet even extreme high power requirements with more than 1000 W/kg peak power. The cells make use of the Recom design ensuring high power charge ability at low internal gas pressure. The paper presents laboratory test results of cells and batteries. (orig.)

Regularities of radium coprecipitation with barium sulfate from salt solutions

International Nuclear Information System (INIS)

Kudryavskij, Yu.P.; Rakhimova, O.V.

2007-01-01

Coprecipitation of radium with barium sulfate from highly concentrated NaCl solutions is studied, including the effects of the initial solution composition, alkaline reagent (CaO, NaOH), supporting electrolyte (NaCl) concentration, and pH. The process is promoted by high NaCl concentration in the initial solution, which is due to structural transformation and change in the sorption activity of the BaSO 4 precipitate in salt solutions. The results obtained were applied to recovery of radium from process solutions during the development and introduction of improved procedure for disinfection and decontamination of waste yielded by chlorination of loparite concentrates [ru

Degradation of diuron in aqueous solution by dielectric barrier discharge

Energy Technology Data Exchange (ETDEWEB)

Feng Jingwei [State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment Nanjing University, Nanjing 210093 (China); Zheng Zheng [State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment Nanjing University, Nanjing 210093 (China)], E-mail: zzheng@nju.edu.cn; Sun Yabing; Luan Jingfei; Wang Zhen; Wang Lianhong; Feng Jianfang [State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment Nanjing University, Nanjing 210093 (China)

2008-06-15

Degradation of diuron in aqueous solution was conducted in a dielectric barrier discharge (DBD) reactor and the proposed degradation mechanism was investigated in detail. The factors that affect the degradation of diuron were examined. The degradation efficiency of diuron and the removal of total organic carbon (TOC) increased with increasing input power, and the degradation of diuron by DBD fitted first-order kinetics. Both strong acidic and alkaline solution conditions could improve diuron degradation efficiency and TOC removal rate. Degradation of diuron could be accelerated or inhibited in the presence of H{sub 2}O{sub 2} depending on the dosage. The degradation efficiency increased dramatically with adding Fe{sup 2+}. The removal of TOC and the amount of the detected Cl{sup -}, NO{sub 3}{sup -} and NH{sub 4}{sup +} were increased in the presence of Fe{sup 2+}. The concentrations of oxalic and acetic acids were almost the same in the absence and presence of Fe{sup 2+}, but high concentration of formic acid was accumulated in the presence of Fe{sup 2+}. The main degradation pathway of diuron by DBD involved a series of dechlorination-hydroxylation, dealkylation and oxidative opening of the aromatic ring processes.

Reinforcement corrosion in alkaline chloride media with reduced oxygen concentrations

International Nuclear Information System (INIS)

Andrade, C.; Fullea, J.; Toro, L.; Martinez, I.; Rebolledo, N.

2013-01-01

It is commonly considered that the corrosion of steel in concrete is controlled by the oxygen content of the pore solution and there are service life models that relate the corrosion rate to the amount of oxygen. It is also commonly believed that in water saturated conditions the oxygen content in the pores is negligible and that underwater there is no risk of depassivation and the corrosion rate is very low. However, the available data on corrosion rates in immersed conditions do not indicate such performance; on the contrary corrosion develops when sufficient chloride reaches the reinforcement. In the present paper, results are presented for tests performed in alkaline chloride solutions that were purged with nitrogen to reduce the oxygen content. The results indicate that at very low oxygen concentrations, corrosion may develop in the presence of chlorides. The presence or absence of corrosion is influenced by the amount of chloride, the corrosion potential and the steel surface condition. (authors)

Formation of ammonia complexes of alkaline earth elements in aqueous solutions

International Nuclear Information System (INIS)

Padar, T.G.; Stupko, T.V.; Isaev, I.D.; Pashkov, G.L.; Mironov, V.E.

1990-01-01

Coefficients of ammonia distribution between aqueous solutions of calcium, strontium, barium and ammonium perchlorate mixtures at ionic strength - 0.50; 1.0 and 1.5 at 298.2 K and ammonia concentrations 0.2-10 mol/dm 3 are measured. Formation of ammonia complexes of M(NH 3 ) n 2+ composition is shown. Logarithms of stepped stability constants for solutions with zero ionic strength for Ca 2+ are: -0.13; -0.25; -0.52 and -0.77, where n=1-4; for Sr 2+ : -0.04; -0.42 and -0.70, where n=1-3 and for Ba 2+ : -0.11; -0.50 and 0.76, where n=1-3

Fundamental Mechanistic Understanding of Electrocatalysis of Oxygen Reduction on Pt and Non-Pt Surfaces: Acid versus Alkaline Media

Directory of Open Access Journals (Sweden)

Nagappan Ramaswamy

2012-01-01

Full Text Available Complex electrochemical reactions such as Oxygen Reduction Reaction (ORR involving multi-electron transfer is an electrocatalytic inner-sphere electron transfer process that exhibit strong dependence on the nature of the electrode surface. This criterion (along with required stability in acidic electrolytes has largely limited ORR catalysts to the platinum-based surfaces. New evidence in alkaline media, discussed here, throws light on the involvement of surface-independent outer-sphere electron transfer component in the overall electrocatalytic process. This surface non-specificity gives rise to the possibility of using a wide-range of non-noble metal surfaces as electrode materials for ORR in alkaline media. However, this outer-sphere process predominantly leads only to peroxide intermediate as the final product. The importance of promoting the electrocatalytic inner-sphere electron transfer by facilitation of direct adsorption of molecular oxygen on the active site is emphasized by using pyrolyzed metal porphyrins as electrocatalysts. A comparison of ORR reaction mechanisms between acidic and alkaline conditions is elucidated here. The primary advantage of performing ORR in alkaline media is found to be the enhanced activation of the peroxide intermediate on the active site that enables the complete four-electron transfer. ORR reaction schemes involving both outer- and inner-sphere electron transfer mechanisms are proposed.

Process for recovering uranium using an alkyl pyrophosphoric acid and alkaline stripping solution

International Nuclear Information System (INIS)

Worthington, R.E.; Magdics, A.

1987-01-01

A process is described for stripping uranium for a pregnant organic extractant comprising an alkyl pyrophosphoric acid dissolved in a substantially water-immiscible organic diluent. The organic extractant contains tetravalent uranium and an alcohol or phenol modifier in a quantity sufficient to retain substantially all the unhydrolyzed alkyl pyrophosphoric acid in solution in the diluent during stripping. The process comprises adding an oxidizing agent to the organic extractant and thereby oxidizing the tetravalent uranium to the +6 state in the organic extractant, and contacting the organic extractant containing the uranium in the +6 state with a stripping solution comprising an aqueous solution of an alkali metal or ammonium carbonate or hydroxide thereby stripping uranium from the organic extractant into the stripping solution. The resulting barren organic extractant containing substantially all of the unhydrolyzed alkyl pyrophosphoric acid dissolved in the diluent is separated from the stripping solution containing the stripped uranium, the barren extractant being suitable for recycle

Rapid Formation of 1D Titanate Nanotubes Using Alkaline Hydrothermal Treatment and Its Photocatalytic Performance

Directory of Open Access Journals (Sweden)

Chin Wei Lai

2015-01-01

Full Text Available One-dimensional (1D titanate nanotubes (TNT were successfully synthesized using alkaline hydrothermal treatment of commercial TiO2 nanopowders in a Teflon lined stainless steel autoclave at 150°C. The minimum time required for the formation of the titanate nanotubes was 9 h significantly. After the hydrothermal processing, the layered titanate was washed with acid and water in order to control the amount of Na+ ions remaining in the sample solutions. In this study, the effect of different reaction durations in a range of 3 h to 24 h on the formation of nanotubes was carried out. As the reaction duration is extended, the changes in structure from particle to tubular shapes of alkaline treated TiO2 were obtained via scanning electron microscope (SEM. Also, the significant impact on the phase transformation and crystal structure of TNT was characterized through XRD and Raman analysis. Indeed, the photocatalytic activity of TNT was investigated through the degradation of methyl orange aqueous solution under the ultraviolet light irradiation. As a result, TNT with reaction duration at 6 h has a better photocatalytic performance than other samples which was correlated to the higher crystallinity of the samples as shown in XRD patterns.

Ethanol production from bamboo using mild alkaline pre-extraction followed by alkaline hydrogen peroxide pretreatment.

Science.gov (United States)

Yuan, Zhaoyang; Wen, Yangbing; Kapu, Nuwan Sella

2018-01-01

A sequential two-stage pretreatment process comprising alkaline pre-extraction and alkaline hydrogen peroxide pretreatment (AHP) was investigated to convert bamboo carbohydrates into bioethanol. The results showed that mild alkaline pre-extraction using 8% (w/w) sodium hydroxide (NaOH) at 100°C for 180min followed by AHP pretreatment with 4% (w/w) hydrogen peroxide (H 2 O 2 ) was sufficient to generate a substrate that could be efficiently digested with low enzyme loadings. Moreover, alkali pre-extraction enabled the use of lower H 2 O 2 charges in AHP treatment. Two-stage pretreatment followed by enzymatic hydrolysis with only 9FPU/g cellulose led to the recovery of 87% of the original sugars in the raw feedstock. The use of the pentose-hexose fermenting Saccharomyces cerevisiae SR8u strain enabled the utilization of 95.7% sugars in the hydrolysate to reach 4.6%w/v ethanol titer. The overall process also enabled the recovery of 62.9% lignin and 93.8% silica at high levels of purity. Copyright © 2017 Elsevier Ltd. All rights reserved.

The influence of alkalinity of portland cement on the absorption characteristics of superabsorbent polymers (SAP) for use in internally cured concrete

Science.gov (United States)

Tabares Tamayo, Juan D.

The concrete industry increasingly emphasizes advances in novel materials that promote construction of more resilient infrastructure. Due to its potential to improve concrete durability, internal curing (IC) of concrete by means of superabsorbent polymers (SAP) has been identified as one of the most promising technologies of the 21st century. The addition of superabsorbent polymers into a cementitious system promotes further hydration of cement by providing internal moisture during the hardening and strength development periods, and thus limits self-desiccation, shrinkage, and cracking. This thesis presents the work performed on the series of cement pastes with varying alkalinity of their pore solutions to provide a better understanding of: (1) the influence of the chemistry of the pore solution (i.e. its level of alkalinity and the type of ionic species present) on the absorption capacity of SAP, and (2) the effectiveness of SAP with different absorption capacities as an internal curing agent. This research work was divided into three stages: (a) materials characterization, (b) measurement of absorption capacity of SAP in synthetic pore solutions, and (c) evaluation of the internal curing effectiveness of SAP. During the first stage (Materials Characterization), pore solutions were extracted from the fresh (5 minutes old) cement pastes prepared using cements with three different levels of alkalinity. The pH values of the extracted solutions were determined (using the pH meter) and their chemical analysis was performed by means of titration (concentration of hydroxyl), ion chromatography (sulfates and chlorides), atomic absorption (AA) and inductively coupled plasma optical emission spectrometry (ICP) (sodium, potassium and calcium). The commercial SAP adopted for this study was used with "as-supplied" gradation and with the finer gradation obtained by grinding the original polymer in the 6850 Cryomilling Freezer/Mill. The physical properties of these SAP's, such

Optimal Surface Amino-Functionalization Following Thermo-Alkaline Treatment of Nanostructured Silica Adsorbents for Enhanced CO2 Adsorption

Directory of Open Access Journals (Sweden)

Obdulia Medina-Juárez

2016-11-01

Full Text Available Special preparation of Santa Barbara Amorphous (SBA-15, mesoporous silica with highly hexagonal ordered, these materials have been carried out for creating adsorbents exhibiting an enhanced and partially selective adsorption toward CO2. This creation starts from an adequate conditioning of the silica surface, via a thermo-alkaline treatment to increase the population of silanol species on it. CO2 adsorption is only reasonably achieved when the SiO2 surface becomes aminated after put in contact with a solution of an amino alkoxide compound in the right solvent. Unfunctionalized and amine-functionalized substrates were characterized through X-ray diffraction, N2 sorption, Raman spectroscopy, electron microscopy, 29Si solid-state Nuclear Magnetic Resonance (NMR, and NH3 thermal programmed desorption. These analyses proved that the thermo-alkaline procedure desilicates the substrate and eliminates the micropores (without affecting the SBA-15 capillaries, present in the original solid. NMR analysis confirms that the hydroxylated solid anchors more amino functionalizing molecules than the unhydroxylated material. The SBA-15 sample subjected to hydroxylation and amino-functionalization displays a high enthalpy of interaction, a reason why this solid is suitable for a strong deposition of CO2 but with the possibility of observing a low-pressure hysteresis phenomenon. Contrastingly, CH4 adsorption on amino-functionalized, hydroxylated SBA-15 substrates becomes almost five times lower than the CO2 one, thus giving proof of their selectivity toward CO2. Although the amount of retained CO2 is not yet similar to or higher than those determined in other investigations, the methodology herein described is still susceptible to optimization.

Influence of alkali, silicate, and sulfate content of carbonated concrete pore solution on mild steel corrosion behavior

International Nuclear Information System (INIS)

L'Hostis, V.; Huet, B.; Tricheux, L.; Idrissi, H.

2010-01-01

The increase in the rebar corrosion rate due to the concrete carbonation is the major cause of reinforced concrete degradation. The aim of this study was to investigate the corrosion behavior of mild steel rebars in simulated carbonated concrete solution. For this purpose, thermodynamic calculations, electrochemical techniques, gravimetric measurements, and surface analyses were used. Thermodynamic investigations of the nature of the interstitial solution provides an estimation of the influence of sulfate (SO 4 2- ) and alkali (Na + , K + ) content on carbonate alkalinity of the CO 2 /H 2 O open system (pCO 2 =0. 3 mbar). in this system, calcium-silicate hydrates (C-S-H) remain thermodynamically unstable and amorphous silica controls silicate aqueous content at 100 ppm. Electrochemical results highlight a decrease in the corrosion rate with increasing carbonate alkalinity and the introduction of silicate. The introduction of sulfate at fixed carbonate alkalinity shows a dual effect: at high carbonate alkalinity, the corrosion rate is increased whereas at low carbonate alkalinity, corrosion rate is decreased. Those results are supported by surface analysis. Authors conclude that silicate and sulfate release from cement hydrates and fixation of alkali on carbonated hydrates are key parameters to estimate mild steel corrosion in carbonated concrete. (authors)

Structure and reactivity of thiazolium azo dyes: UV-visible, resonance Raman, NMR, and computational studies of the reaction mechanism in alkaline solution.

Science.gov (United States)

Abbott, Laurence C; Batchelor, Stephen N; Moore, John N

2013-03-07

UV-visible absorption, resonance Raman, and (1)H NMR spectroscopy, allied with density functional theory (DFT) calculations, have been used to study the structure, bonding, and alkaline hydrolysis mechanism of the cationic thiazloium azo dye, 2-[2-[4-(diethylamino)phenyl]diazenyl]-3-methyl-thiazolium (1a), along with a series of six related dyes with different 4-dialkylamino groups and/or other phenyl ring substituents (2a-c, 3a-c) and the related isothiazolium azo dye, 5-[2-[4-(dimethylamino)phenyl]diazenyl]-2-methyl-isothiazolium (4). These diazahemicyanine dyes are calculated to have a similar low-energy structure that is cis, trans at the (iso)thiazolium-azo group, and for which the calculated Raman spectra provide a good match with the experimental data; the calculations on these structures are used to assign and discuss the transitions giving rise to the experimental spectra, and to consider the bonding and its variation between the dyes. UV-visible, Raman, and NMR spectra recorded from minutes to several weeks after raising the pH of an aqueous solution of 1a to ca. 11.5 show that the dominant initial step in the reaction is loss of diethylamine to produce a quinonimine (ca. hours), with subsequent reactions occurring on longer time scales (ca. days to weeks); kinetic analyses give a rate constant of 2.6 × 10(-2) dm(3) mol(-1) s(-1) for reaction of 1a with OH(-). UV-visible spectra recorded on raising the pH of the other dyes in solution show similar changes that are attributed to the same general reaction mechanism, but with different rate constants for which the dependence on structure is discussed.

Production of alkaline proteases by alkalophilic Bacillus subtilis ...

African Journals Online (AJOL)

Tuoyo Aghomotsegin

2016-11-23

Nov 23, 2016 ... Key words: Production, alkaline protease, Bacillus subtilis, animal wastes, enzyme activity. ... Generally, alkaline proteases are produced using submerged fermentation .... biopolymer concentrations were reported to have an influence ... adding nitrogenous compounds stimulate microorganism growth and ...

Safety of an alkalinizing buffer designed for inhaled medications in humans.

Science.gov (United States)

Davis, Michael D; Walsh, Brian K; Dwyer, Scott T; Combs, Casey; Vehse, Nico; Paget-Brown, Alix; Pajewski, Thomas; Hunt, John F

2013-07-01

Airway acidification plays a role in disorders of the pulmonary tract. We hypothesized that the inhalation of alkalinized glycine buffer would measurably alkalinize the airways without compromising lung function or causing adverse events. We evaluated the safety of an inhaled alkaline glycine buffer in both healthy subjects and in subjects with stable obstructive airway disease. This work includes 2 open-label safety studies. The healthy controls were part of a phase 1 safety study of multiple inhalations of low-dose alkaline glycine buffer; nebulized saline was used as a comparator in 8 of the healthy controls. Subsequently, a phase 2 study in subjects with stable obstructive airway disease was completed using a single nebulized higher-dose strategy of the alkaline inhalation. We studied 20 non-smoking adults (10 healthy controls and 10 subjects with obstructive airway disease), both at baseline and after inhalation of alkaline buffer. We used spirometry and vital signs as markers of clinical safety. We used changes in fraction of exhaled nitric oxide (NO) and exhaled breath condensate (EBC) pH as surrogate markers of airway pH modification. Alkaline glycine inhalation was tolerated by all subjects in both studies, with no adverse effects on spirometric parameters or vital signs. Airway alkalinization was confirmed by a median increase in EBC pH of 0.235 pH units (IQR 0.56-0.03, P = .03) in subjects after inhalation of the higher-dose alkaline buffer (2.5 mL of 100 mmol/L glycine). Alkalinization of airway lining fluid is accomplished with inhalation of alkaline glycine buffer and causes no adverse effects on pulmonary function or vital signs.

Alkalinity and trophic state regulate aquatic plant distribution in Danish lakes

DEFF Research Database (Denmark)

Vestergaard, Ole Skafte; Sand-Jensen, Kaj

2000-01-01

distinct differences in the distribution of species and growth forms among the lakes. The lakes separated into five groups of characteristic species compositions. Alkalinity was the main factor responsible for the species distribution. Lakes of high alkalinity were dominated by vascular plants...... of the elodeid growth form, lakes of intermediate alkalinity contained a variety of elodeids and vascular plants of the isoetid growth form, while lakes of low alkalinity and low pH had several isoetids and bryophytes, but very few elodeids. Alkalinity is a close descriptor of the bicarbonate concentration...

Alkaline lixiviation of uranium in granitic pegmatite

International Nuclear Information System (INIS)

Jambor, S.

1980-06-01

The work described herein concerns the determination of the experimental optimum conditions for the alkaline lixiviation of uranium based on the following parameters: time, pH, temperature, density and grane size. The samples were obtained from the Supamo complex, near the Currupia river in the Piar District of the Bolivar State in Venezuela. They have a granitic composition and graphitic texture. The uranium was found in them as a secondary oxidized mineral of green-yellow colour localized in fractures fissures, intergranular spaces and also in the mica as. Secondary uranitite. The lixiviation process was carried out using Na 2 CO 3 /NaHCO 3 buffer solution and for 100 gr. samples the best values for an efficient process were found by using 170 mesh grane size and 500 ml of pH buffer at 70 0 C for a 24 hour time period. (author)

Multi-layer membrane model for mass transport in a direct ethanol fuel cell using an alkaline anion exchange membrane

Science.gov (United States)

Bahrami, Hafez; Faghri, Amir

2012-11-01

A one-dimensional, isothermal, single-phase model is presented to investigate the mass transport in a direct ethanol fuel cell incorporating an alkaline anion exchange membrane. The electrochemistry is analytically solved and the closed-form solution is provided for two limiting cases assuming Tafel expressions for both oxygen reduction and ethanol oxidation. A multi-layer membrane model is proposed to properly account for the diffusive and electroosmotic transport of ethanol through the membrane. The fundamental differences in fuel crossover for positive and negative electroosmotic drag coefficients are discussed. It is found that ethanol crossover is significantly reduced upon using an alkaline anion exchange membrane instead of a proton exchange membrane, especially at current densities higher than 500 A m

Defluoridation of drinking water by combined electrocoagulation: effects of the molar ratio of alkalinity and fluoride to Al(III).

Science.gov (United States)

Zhao, Hua-Zhang; Yang, Wei; Zhu, Jun; Ni, Jin-Ren

2009-03-01

The defluoridation efficiency (epsilon(F)) of electrocoagulation (EC) is closely related to the pH level of the F(-)-containing solution. The pH level usually needs to be adjusted by adding acid in order to obtain the highest epsilon(F) for the F(-)-containing groundwater. The use of combined EC (CEC), which is the combination of chemical coagulation with EC, was proposed to remove fluoride from drinking water for the first time in this study. The optimal scheme for the design and operation of CEC were obtained through experiments on the treatment of F(-)-containing groundwater. It was found, with OH(-) being the only alkalinity of the raw water, that the highest efficiency would be obtained when the molar ratio of alkalinity and fluoride to Al(III) (gamma(Alkalinity+F)) was controlled at 3.0. However, when the raw water contained HCO(3)(-) alkalinity, a correction coefficient was needed to correct the concentration of HCO(3)(-) to obtain the optimal defluoridation condition of gamma(Alkalinity+F)=3.0 for CEC. The correction coefficient of HCO(3)(-) concentration was concluded as 0.60 from the experiment. For the practical F(-)-containing groundwater treatment, CEC can achieve similar epsilon(F) as an acid-adding EC process. The consumption of aluminum electrode was decreased in CEC. The energy consumption also declined greatly in CEC, which is less than one third of that in the acid-adding EC process.

Production of alkaline proteases by alkalophilic Bacillus subtilis ...

African Journals Online (AJOL)

Tuoyo Aghomotsegin

2016-11-23

Nov 23, 2016 ... A new strain of Bacillus sp. was isolated from alkaline soil, which was able to produce extracellular alkaline ... rice and dates (Khosravi-Darani et al., 2008), protein by- products from lather ..... Pigeon pea waste as a novel ...

Aspects of the structure and solution chemistry of some technetium-tripolyphosphate complexes

International Nuclear Information System (INIS)

Miller, G.G.

1983-01-01

Several distinctly different complexes of Tc(III) and Tc(IV) with the ligand tripolyphosphate were prepared and studied electrochemically. In acidic solution, a transient Tc(III) species was observed, the electrochemical behavior of which proves that it is not monomeric in Tc and strongly suggests that it is a dimer. This material is radically different in its polarographic behavior from the Tc(III) complex resulting from the controlled potential electrolysis of TcO 4 - at a mercury pool cathode in the same electrolyte. The latter, air sensitive, complex can be reversibly oxidized to a Tc(IV) complex which is stable towards further oxidation but which undergoes hydrolysis in both acidic and alkaline media. The rate law for the hydrolysis in basic solution is: rate = 582 I mol -1 min -1 [Tc(IV)][OH - ]. The hydrolytic reaction in acidic solution is accelerated by hydrogen ion, indicating that a mechanism different from that in basic media is involved. Tc(IV) tripolyphosphate complexes prepared by ligand exchange reactions of TcBr 6 2- were shown by polarography to be different from the complexes prepared electrochemically. The gel permeation chromatographic behavior of one ligand substitution product showed it to be polymeric with a limiting tripolyphosphate to technetium ratio of 1:1

Study of the radiolysis of tetracycline hidrochloride in aerated aqueous solutions

International Nuclear Information System (INIS)

Guedes, S.M.L.; Vasconcellos, M.B.A.

1983-01-01

The radiolysis of tetracycline hydrochloride (TC) was studied in neutral, acid and alkaline aerated solutions, by electron spin resonance spectroscopy at 77K. The paramagnetic species observed are: H.; OH.; HO 2 .; e - trapped and impurity radical. The reaction mechanism shows that the solute reacts with the solvent before the radiolysis and produces H + ions, as a consequence of the ionization of tricarbonylmethane group. The H + ions react with the e - from the radiolysis of water and produce HO 2 in the presence of O 2 . The interaction of TC with the alkaline solvent favours the interaction between gamma rays and solute. The products formed in the interaction of solute with the solvent before the radiolysis, as a consenquence of the ionization of TC, according to the pH of the solution, are of fundamental importance in the interaction of gamma rays with the solute. A crude estimate of the average distance that the e - is able to travel through solvent molecules before its capture by the solute was obtained in these 0.1N, 0.5N and 1.0N NaOH aqueous solutions. Until [TC] - travels more in solutions that contain less [NaOH]. In higher [TC] the e - travels through 680 solvent molecules. In order to explain the selective capture of the e3- by solute molecules, a simple model is suggested based on the existence of channel walls of solvent molecules where the electrical atraction betwwed Na + and e - influences the collision frequency and the energy loss. (Author) [pt

Novel inorganic materials for polymer electrolyte and alkaline fuel cells

Science.gov (United States)

Tadanaga, Kiyoharu

2012-06-01

Inorganic materials with high ionic conductivity must have big advantages for the thermal and long term stability when the materials are used as the electrolyte of fuel cells. In the present paper, novel ionic conductive inorganic materials for polymer electrolyte fuel cells (PEFCs) and all solid state alkaline fuel cells (AFCs) that have been developed by our group have been reviewed. PEFCs which can operate in temperature range from 100 to 200 °C are intensively studied because of some advantages such as reduction of CO poisoning of Pt catalyst and acceleration of electrode reactions. We showed that the fuel cells using the composite membranes prepared from phosphosilicate gel powder and polyimide precursor can operate in the temperature range from 30 to 180 °C. We also found that the inorganic-organic hybrid membranes with acid-base pairs from 3-aminopropyl triethoxy silane and H2SO4 or H3PO4 show high proton conductivity under dry atmosphere, and the membranes are thermally stable at intermediate temperatures. On the other hand, because the use of noble platinum is the serious problem for the commercialization of PEFCs and because oxidation reactions are usually faster than those of acid-type fuel cells, alkaline type fuel cells, in which a nonplatinum catalyst can be used, are attractive. Recently, we have proposed an alkaline-type direct ethanol fuel cell (DEFC) using a natural clay electrolyte with non-platinum catalysts. So-called hydrotalcite clay, Mg-Al layered double hydroxide intercalated with CO32- (Mg-Al CO32- LDH), has been proved to be a hydroxide ion conductor. An alkalinetype DEFC using Mg-Al CO32- LDH as the electrolyte and aqueous solution of ethanol and potassium hydroxide as a source of fuel exhibited excellent electrochemical performance.

IUPAC-NIST Solubility Data Series. 95. Alkaline Earth Carbonates in Aqueous Systems. Part 2. Ca

International Nuclear Information System (INIS)

De Visscher, Alex; Vanderdeelen, Jan

2012-01-01

The alkaline earth carbonates are an important class of minerals. This article is part of a volume in the IUPAC-NIST Solubility Data Series that compiles and critically evaluates solubility data of the alkaline earth carbonates in water and in simple aqueous electrolyte solutions. Part 1 outlined the procedure adopted in this volume, and presented the beryllium and magnesium carbonates. Part 2, the current paper, compiles and critically evaluates the solubility data of calcium carbonate. The chemical forms included are the anhydrous CaCO 3 types calcite, aragonite, and vaterite, the monohydrate monohydrocalcite (CaCO 3 · H 2 O), the hexahydrate ikaite (CaCO 3 ·6H 2 O), and an amorphous form. The data were analyzed with two model variants, and thermodynamic data of each form consistent with each of the models and with the CODATA key values for thermodynamics are presented.

Fiber degradability of sugar cane bagasse treated by alkaline solutions, through the “in situ” nylon bag technique

Directory of Open Access Journals (Sweden)

Sérgio Carlo Franco Morgulis

1996-09-01

treated bagasse (A was higher than in B or C treatments; degradability of B was higher than in C at 72h and 96h of incubation time. NDF degradability at 48 hour incubation time showed the following results: A = 74.0%; B = 41.6% and C = 35.7%. In conclusion, alkaline (NaOH and wood ash treated sugar cane bagasse improves ruminal degradability, and NaOH is better than wood ash.

The influence of lake water alkalinity and humic substances on particle dispersion and lanthanum desorption from a lanthanum modified bentonite

DEFF Research Database (Denmark)

Reitzel, Kasper; Balslev, Kristiane Astrid; Jensen, Henning S

2017-01-01

A 12 days laboratory study on potential desorption of Lanthanum (La) from a commercial La modified clay (Phoslock) was conducted using lake water from 17 Danish lakes with alkalinities between 0.02 and 3.7 meq L-1and varying concentrations of DOC and humic acids (HA's). A similar study...... was conducted in artificial lake water with alkalinities from 0 to 2.5 meq L-1in order to exclude interference from dissolved HA's. To test if La in solution (FLa) was associated with fine particles, the water samples were filtered sequentially through three filter sizes (1.2 μm, 0.45 μm and 0.2 μm...... at low alkalinities. In addition, this study showed that HA's seem to increase the FLa concentrations in soft water lakes, most likely through complexation of La retained in the Phoslock matrix. In summary, we conclude that elevated La concentrations in lake water after a Phoslock treatment should only...

Effects of acid and alkaline based surface preparations on spray deposited cerium based conversion coatings on Al 2024-T3

Energy Technology Data Exchange (ETDEWEB)

Pinc, W. [Department of Materials Science Engineering, Materials Research Center, Missouri University of Science and Technology, Rolla, MO 65409 (United States)], E-mail: wrphw5@mst.edu; Geng, S.; O' Keefe, M.; Fahrenholtz, W.; O' Keefe, T. [Department of Materials Science Engineering, Materials Research Center, Missouri University of Science and Technology, Rolla, MO 65409 (United States)

2009-01-15

Cerium based conversion coatings were spray deposited on Al 2024-T3 and characterized to determine the effect of surface preparation on the deposition rate and surface morphology. It was found that activation of the panel using a 1-wt.% sulfuric acid solution increased the coating deposition rate compared to alkaline cleaning alone. Analysis of the surface morphology of the coatings showed that the coatings deposited on the acid treated panels exhibited fewer visible cracks compared to coatings on alkaline cleaned panels. Auger electron spectroscopy depth profiling showed that the acid activation decreased the thickness of the aluminum oxide layer and the concentration of magnesium on the surface of the panels compared to the alkaline treatment. Additionally, acid activation increased the copper concentration at the surface of the aluminum substrate. Based on the results, the acid based surface treatment appeared to expose copper rich intermetallics, thus increasing the number of cathodic sites on the surface, which led to an overall increase in the deposition rate.

Overexpression of Human Bone Alkaline Phosphatase in Pichia Pastoris

Science.gov (United States)

Karr, Laurel; Malone, Christine, C.; Rose, M. Franklin (Technical Monitor)

2000-01-01

The Pichiapastoris expression system was utilized to produce functionally active human bone alkaline phosphatase in gram quantities. Bone alkaline phosphatase is a key enzyme in bone formation and biomineralization, yet important questions about its structural chemistry and interactions with other cellular enzymes in mineralizing tissues remain unanswered. A soluble form of human bone alkaline phosphatase was constructed by deletion of the 25 amino acid hydrophobic C-terminal region of the encoding cDNA and inserted into the X-33 Pichiapastoris strain. An overexpression system was developed in shake flasks and converted to large-scale fermentation. Alkaline phosphatase was secreted into the medium to a level of 32mgAL when cultured in shake flasks. Enzyme activity was 12U/mg measured by a spectrophotometric assay. Fermentation yielded 880mgAL with enzymatic activity of 968U/mg. Gel electrophoresis analysis indicates that greater than 50% of the total protein in the fermentation is alkaline phosphatase. A purification scheme has been developed using ammonium sulfate precipitation followed by hydrophobic interaction chromatography. We are currently screening crystallization conditions of the purified recombinant protein for subsequent X-ray diffraction analyses. Structural data should provide additional information on the role of alkaline phosphatase in normal bone mineralization and in certain bone mineralization anomalies.

Zeolite A synthesized from alkaline assisted pre-activated halloysite for efficient heavy metal removal in polluted river water and industrial wastewater.

Science.gov (United States)

Meng, Qingpeng; Chen, Hong; Lin, Junzhong; Lin, Zhang; Sun, Junliang

2017-06-01

High quality zeolite A was synthesized through a hydrothermal process using alkaline-assisted pre-activated halloysite mineral as the alumina and silica source. The synthesis conditions employed in this study were finely tuned by varying the activating temperature, sodium hydroxide content, water content and Si/Al ratio. The obtained zeolite A showed excellent adsorption properties for both single metal cation solutions and mixed cation solutions when the concentrations of the mixed cations were comparable with those in polluted natural river water and industrial wastewater. High adsorptive capacities for Ag + (123.05mg/g) and Pb 2+ (227.70mg/g) were achieved using the synthesized zeolite A. This observation indicates that the zeolite A synthesized from alkaline-assisted pre-activated halloysite can be used as a low-cost and relatively effective adsorbent to purify heavy metal cation polluted natural river water and industrial wastewater. Copyright © 2016. Published by Elsevier B.V.

On the existence of global strong solutions to the equations modeling a motion of a rigid body around a viscous fluid

Czech Academy of Sciences Publication Activity Database

Nečasová, Šárka; Wolf, J.

2016-01-01

Roč. 36, č. 3 (2016), s. 1539-1562 ISSN 1078-0947 R&D Projects: GA ČR GA13-00522S Institutional support: RVO:67985840 Keywords : incompressible fluid * motion of rigid body * strong solutions Subject RIV: BA - General Mathematics Impact factor: 1.099, year: 2016 http://www.aimsciences.org/journals/displayArticlesnew.jsp?paperID=11589

Evaluation of some bean lines tolerance to alkaline soil

Directory of Open Access Journals (Sweden)

Abeer A. Radi

2012-01-01

Full Text Available Introduction: In less arid climates, salts are less concentrated and sodium dominates in carbonate and bicarbonate forms, which enhance the formation of alkaline soils. The development and identification of salt-tolerant crop cultivars or lines would complement salt management programs to improve the productivity and yields of salt stressed plants.Materials and methods: This work was to study the evaluation of alkalinity tolerance of some bean lines grown under different levels of sodium carbonate (Na2CO3 to select the most alkalinity tolerant lines versus the most-sensitive ones out of 6 lines of the test plants.Results: The symptoms induced by alkalinity included reduction in root, shoot growth, and leaf area which were more severe in some bean lines. Potassium leakage was severely affected by alkalinity in some lines at all tested levels, while in some others a moderate damage was manifested only at the higher levels. The increase in Na2CO3 level was associated with a gradual fall in chlorophyll a and b biosynthesis of all the test bean lines. However, alkalinity at low and moderate levels had a favorable effect on the biosynthesis of carotenoids in all the test bean lines. The increase in Na2CO3 supply had a considerable stimulatory effect on sodium accumulation, while potassium accumulation fluctuated in organs of bean lines.Conclusion: Assiut 1104 out of all the different lines investigated was found to display the lowest sensitivity to alkalinity stress, while Assiut 12/104 was the most sensitive one.

Novel package for inhibition of aluminium corrosion in alkaline solutions

Energy Technology Data Exchange (ETDEWEB)

Abdel-Gaber, A.M., E-mail: ashrafmoustafa@yahoo.com [Chemistry Department, Faculty of Science, Alexandria University, Ibrahimia, P.O. Box 426, Alexandria 21321 (Egypt); Khamis, E.; Abo-Eldahab, H.; Adeel, Sh. [Chemistry Department, Faculty of Science, Alexandria University, Ibrahimia, P.O. Box 426, Alexandria 21321 (Egypt)

2010-11-01

Inhibition of aluminium corrosion in 2 M sodium hydroxide solution by a package composed of the cationic surfactant cetyl trimethyl ammonium bromide (CTAB) and lupine seed extract has been investigated employing different electrochemical techniques and chemical gasometry measurements. Potentiodynamic polarization curve measurements showed that lupine seed extract controls both the anodic dissolution of aluminium and the hydrogen gas evolved at the cathodic sites of aluminium surface. Nyquist plots showed two capacitive semicircles in the high and low frequency regions separated by an inductive loop at intermediate frequencies. The inductive loop may be explained by the occurrence of adsorbed intermediates on the surface. A proposed equivalent circuit was used to analyse the impedance spectra for aluminium in NaOH solutions. The corrosion inhibition data have been analysed using different isotherms. The results showed excellent agreement between the kinetic-thermodynamic model and Flory-Huggins isotherm. Gasometry measurements showed that the Inhibitive effect of the surfactant increases at a composition around its critical micelle concentration (cmc). The presence of both the surfactant and lupine seed extract did not indicate synergistic action between them. The mode of adsorption of the surfactant molecules corresponding to their structure is also discussed.

Novel package for inhibition of aluminium corrosion in alkaline solutions

International Nuclear Information System (INIS)

Abdel-Gaber, A.M.; Khamis, E.; Abo-Eldahab, H.; Adeel, Sh.

2010-01-01

Inhibition of aluminium corrosion in 2 M sodium hydroxide solution by a package composed of the cationic surfactant cetyl trimethyl ammonium bromide (CTAB) and lupine seed extract has been investigated employing different electrochemical techniques and chemical gasometry measurements. Potentiodynamic polarization curve measurements showed that lupine seed extract controls both the anodic dissolution of aluminium and the hydrogen gas evolved at the cathodic sites of aluminium surface. Nyquist plots showed two capacitive semicircles in the high and low frequency regions separated by an inductive loop at intermediate frequencies. The inductive loop may be explained by the occurrence of adsorbed intermediates on the surface. A proposed equivalent circuit was used to analyse the impedance spectra for aluminium in NaOH solutions. The corrosion inhibition data have been analysed using different isotherms. The results showed excellent agreement between the kinetic-thermodynamic model and Flory-Huggins isotherm. Gasometry measurements showed that the Inhibitive effect of the surfactant increases at a composition around its critical micelle concentration (cmc). The presence of both the surfactant and lupine seed extract did not indicate synergistic action between them. The mode of adsorption of the surfactant molecules corresponding to their structure is also discussed.

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

International Nuclear Information System (INIS)

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

1995-01-01

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

A scanning tunneling microscopy investigation of the phases formed by the sulfur adsorption on Au(100) from an alkaline solution of 1,4-piperazine(bis)-dithiocarbamate of potassium

Energy Technology Data Exchange (ETDEWEB)

Martínez, Javier A. [Instituto de Ciencia y Tecnología de Materiales (IMRE), Universidad de La Habana, Zapata y G, El Vedado, Plaza de la Revolución, La Habana 10400 (Cuba); Valenzuela B, José [Centro de Nanociencias y Nanotecnología (CNyN), Universidad Nacional Autónoma de México (UNAM) , km 107 Carretera Tijuana-Ensenada, Ensenada, BC 22860 (Mexico); Cao Milán, R. [Facultad de Química, Universidad de La Habana, Zapata y G, El Vedado, Plaza de la Revolución, La Habana 10400 (Cuba); Herrera, José [Instituto de Ciencia y Tecnología de Materiales (IMRE), Universidad de La Habana, Zapata y G, El Vedado, Plaza de la Revolución, La Habana 10400 (Cuba); Farías, Mario H. [Centro de Nanociencias y Nanotecnología (CNyN), Universidad Nacional Autónoma de México (UNAM) , km 107 Carretera Tijuana-Ensenada, Ensenada, BC 22860 (Mexico); Hernández, Mayra P., E-mail: mayrap@fisica.uh.cu [Instituto de Ciencia y Tecnología de Materiales (IMRE), Universidad de La Habana, Zapata y G, El Vedado, Plaza de la Revolución, La Habana 10400 (Cuba)

2014-11-30

Highlights: • New phases of sulfur on gold: hexamer and (√(2)×√(2)) were observed by STM. • Hexamers and (√(2)×√(2)) structures coexist with well-known octomers. • Formation of sulfur multilayer by K{sub 2}DTC{sub 2}pz hydrolysis under alkaline condition. • Top octomer layer have dynamic behavior while (√(2)×√(2)) and hexamer were static. • A model is presented to explain sulfur multilayer formation on Au(100). - Abstract: Piperazine-dithiocarbamate of potassium (K{sub 2}DTC{sub 2}pz) was used as a new precursor for the spontaneous deposition of sulfur on the Au(100) surface in alkaline solution. Two new sulfur phases were studied by scanning tunneling microscopy (STM). These phases were formed by six sulfur atoms (S{sub 6} phase, hexamer) and by four sulfur atoms (S{sub 4} phase, tetramer with (√(2)×√(2)) structure), and they were observed in coexistence with the well-known quasi-square patterns formed by eight sulfur atoms (S{sub 8} phase, octomer). A model was proposed where sulfur multilayers were formed by a (√(2)×√(2)) phase adsorbed directly on the gold surface while one of the other structures: hexamers or octomers were deposited on top. Sulfur layers were formed on gold terraces, vacancies and islands produced by lifting reconstructed surface. Sequential high-resolution STM images allowed the direct observation of the dynamic of the octomers, while the (√(2)×√(2)) structure remained static. Images also showed the reversible association/dissociation of the octomer.

A scanning tunneling microscopy investigation of the phases formed by the sulfur adsorption on Au(100) from an alkaline solution of 1,4-piperazine(bis)-dithiocarbamate of potassium

International Nuclear Information System (INIS)

Martínez, Javier A.; Valenzuela B, José; Cao Milán, R.; Herrera, José; Farías, Mario H.; Hernández, Mayra P.

2014-01-01

Highlights: • New phases of sulfur on gold: hexamer and (√(2)×√(2)) were observed by STM. • Hexamers and (√(2)×√(2)) structures coexist with well-known octomers. • Formation of sulfur multilayer by K 2 DTC 2 pz hydrolysis under alkaline condition. • Top octomer layer have dynamic behavior while (√(2)×√(2)) and hexamer were static. • A model is presented to explain sulfur multilayer formation on Au(100). - Abstract: Piperazine-dithiocarbamate of potassium (K 2 DTC 2 pz) was used as a new precursor for the spontaneous deposition of sulfur on the Au(100) surface in alkaline solution. Two new sulfur phases were studied by scanning tunneling microscopy (STM). These phases were formed by six sulfur atoms (S 6 phase, hexamer) and by four sulfur atoms (S 4 phase, tetramer with (√(2)×√(2)) structure), and they were observed in coexistence with the well-known quasi-square patterns formed by eight sulfur atoms (S 8 phase, octomer). A model was proposed where sulfur multilayers were formed by a (√(2)×√(2)) phase adsorbed directly on the gold surface while one of the other structures: hexamers or octomers were deposited on top. Sulfur layers were formed on gold terraces, vacancies and islands produced by lifting reconstructed surface. Sequential high-resolution STM images allowed the direct observation of the dynamic of the octomers, while the (√(2)×√(2)) structure remained static. Images also showed the reversible association/dissociation of the octomer

DETERMINATION OF SULFUR DIOXIDE, NITROGEN OXIDES, AND CARBON DIOXIDE IN EMISSIONS FROM ELECTRIC UTILITY PLANTS BY ALKALINE PERMANGANATE SAMPLING AND ION CHROMATOGRAPHY

Science.gov (United States)

A manual 24-h integrated method for determining SO2, NOx, and CO2 in emissions from electric utility plants was developed and field tested downstream from an SO2 control system. Samples were collected in alkaline potassium permanganate solution contained in restricted-orifice imp...

Irrigation water acidification to neutralize alkalinity for nursery crop production: Substrate pH, electrical conductivity, nutrient concentrations, and plant nutrition and growth

Science.gov (United States)

Liming agents in irrigation water, typically associated with carbonates and bicarbonates of calcium and magnesium, contribute to water alkalinity. Repeated application of LA to container crops can cause media-solution pH to rise overtime, that uncorrected, can lead to a nutrient availability imbalan...

Hydroxide Self-Feeding High-Temperature Alkaline Direct Formate Fuel Cells.

Science.gov (United States)

Li, Yinshi; Sun, Xianda; Feng, Ying

2017-05-22

Conventionally, both the thermal degradation of the anion-exchange membrane and the requirement of additional hydroxide for fuel oxidation reaction hinder the development of the high-temperature alkaline direct liquid fuel cells. The present work addresses these two issues by reporting a polybenzimidazole-membrane-based direct formate fuel cell (DFFC). Theoretically, the cell voltage of the high-temperature alkaline DFFC can be as high as 1.45 V at 90 °C. It has been demonstrated that a proof-of-concept alkaline DFFC without adding additional hydroxide yields a peak power density of 20.9 mW cm -2 , an order of magnitude higher than both alkaline direct ethanol fuel cells and alkaline direct methanol fuel cells, mainly because the hydrolysis of formate provides enough OH - ions for formate oxidation reaction. It was also found that this hydroxide self-feeding high-temperature alkaline DFFC shows a stable 100 min constant-current discharge at 90 °C, proving the conceptual feasibility. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Charge-Discharge Properties of the Surface-Modified ZrNi Alloy Electrode with Different Degrees of Boiling Alkaline Treatment

Directory of Open Access Journals (Sweden)

Akihiro Matsuyama

2016-09-01

Full Text Available Charge-discharge properties of the surface-modified ZrNi negative electrodes with different degrees of boiling alkaline treatment were investigated. The boiling alkaline treatment was performed by immersing the ZrNi electrode in a boiling 6 M KOH aqueous solution for 2 h or 4 h. The initial discharge capacity for the untreated ZrNi negative electrode was 21 mAh·g−1, but it was increased to 114 mAh·g−1 and 308 mAh·g−1 after the boiling alkaline treatments for 2 h and 4 h, respectively. The discharge capacity for the ZrNi negative electrode after the treatment for 2 h steadily increased with repeating charge-discharge cycles as well as that of the untreated electrode, whereas that for the ZrNi negative electrode after the 4 h treatment greatly decreased. The high rate of dischargeability was improved with an increase in the treatment period of time, and the charge-transfer resistance was drastically decreased. Scanning electron microscopy (SEM and electron dispersive X-ray spectroscopy demonstrated the ZrO2 passive layer on the ZrNi alloy surface was removed by the boiling alkaline treatment to form a porous morphology containing Ni(OH2, which can be reduced to Ni during charging, leading to the reduction of a barrier for the charge-discharge reactions.

Mathematical simulation and calculation of continuous countercurrent process of ion-exchange extraction of strontium from strongly mineralized solutions

International Nuclear Information System (INIS)

Nikashina, V.A.; Venitsianov, E.V.; Ivanov, V.A.; Gur'yanova, L.N.; Nikolaev, N.P.; Baturova, L.L.; Moskovskij Gosudarstvennyj Univ., Moscow

1993-01-01

A program 'Countercurrent' is developed for the simulation of a continuous ion-exchange extraction of strontium from the strongly mineralized solutions containing NaCl and CaCl 2 using carboxylic cation exchanger KB-4 in countercurrent columns. The use of the program allows one to calculate the consitions of Ca and Sr separation depending on the modes of operation at the stage of sorption as well as regeneration, to calculate a residual Sr content on an overloaded sorbent and Sr separation on an incompletely regenerated KB-4, and to find the optimal separation conditions

The Estimation Formation Alkaline In The Proses Desalination MSF

International Nuclear Information System (INIS)

Latiffah, Siti Nurul

2000-01-01

Already to go on estimation phenomena formation alkaline scale of a seawater. In desalination system seawater on MSF to go on scale by a thermal decomposition HCO sub.3- ion and hydrolysis carbonate ion with water on the temperature operation. The varieties alkaline scale in attached on tube surface, while reduced efficiency heat transfer and to raise corrosion attack to structure material is caused all this high cost. Estimation to take please which a sum step by step decomposition ion bicarbonate from then information scale which carbonate and hydroxyl ion. The various scale maximal is alkaline form is a calcium carbonate = 116,5 gram per meter cubic the various sedimentation is alkaline and magnesium hydroxide = 67,57 gram per meter cubic

Physicochemical Properties of Defatted Rambutan (Nephelium lappaceum) Seed Flour after Alkaline Treatment.

Science.gov (United States)

Eiamwat, Jirawat; Wanlapa, Sorada; Kampruengdet, Sukit

2016-03-31

Rambutan seeds were subjected to SC-CO₂ extraction at 35 MPa, 45 °C to obtain defatted rambutan seed flour. Its physicochemical properties before and after treatment with alkali solution using 0.075 N NaOH were investigated. Alkali-treated flour had a significant increment in bulk density, swelling power, water adsorption capacity, emulsion capacity and stability but a reduction in turbidity, solubility and oil absorption capacity. Pasting measurements showed peak viscosity, breakdown, setback and final viscosity increased significantly for the alkali-treated flour, while pasting temperature decreased. The alkaline treatment decreased the least gelation concentration, but increased the apparent viscosity.

Production of alkaline protease by Teredinobacter turnirae cells ...

African Journals Online (AJOL)

The conditions for immobilizing the new alkaline protease-producing bacteria strain Teredinobacter turnirae by entrapment in calcium alginate gel were investigated. The influence of alginate concentration (20, 25 and 30 g/l) and initial cell loading (ICL) on enzyme production were studied. The production of alkaline ...

Selectivity of some basic solutes on a poly(methyltetradecylsiloxane)-silica stationary phase.

Science.gov (United States)

Borges, Endler M; Collins, Carol H

2011-11-01

Complex analyses of polar compounds, especially basic ones, require more selective stationary phases. The present paper describes a stationary phase prepared by thermal immobilization of poly(methyltetradecylsiloxane) onto chromatographic silica (PMTDS-SiO(2)). This stationary phase presents hydrophobic and ion-exchange interactions that confer both high retention and unique selectivities for basic solutes. The influence of ion-exchange interactions is confirmed by the increase in retention factors of basic solutes when the mobile-phase pH changes from acidic to neutral and by the decrease in retention factors when the mobile-phase pH changes from neutral to alkaline. The ion-exchange properties of the stationary phase are enriched in neutral mobile phase (pH 7-7.5) using soft Lewis bases such as tricine and tris as buffers but are suppressed in both acidic (pH 2.5-6) and highly alkaline mobile phases (pH≤10). Increasing both temperature and flow rate permits more rapid separations while maintaining the selectivity. The stability of the stationary phase is evaluated with acid, neutral and alkaline mobile phases. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

High temperature and pressure alkaline electrolysis

DEFF Research Database (Denmark)

Allebrod, Frank; Chatzichristodoulou, Christodoulos; Mogensen, Mogens Bjerg

2013-01-01

Alkaline electrolyzers have proven to operate reliable for decades on a large scale, but in order to become commercially attractive and compete against conventional technologies for hydrogen production, the production and investment costs have to be reduced. This may occur by increasing the opera......Alkaline electrolyzers have proven to operate reliable for decades on a large scale, but in order to become commercially attractive and compete against conventional technologies for hydrogen production, the production and investment costs have to be reduced. This may occur by increasing...

Elaboration and test of the method of separation of alkaline metals ions with tin phosphate

International Nuclear Information System (INIS)

Smirnov, G.I.; Chernyak, A.S.; Kostromina, O.N.; Kachur, N.Ya.; Shpeyzer, B.G.

1986-01-01

Present work is devoted to elaboration and test of the method of separation of alkaline metals ions with tin phosphate. Thus, the isotherms of sorption of lithium, sodium, potassium, rubidium and cesium ions with amorphous tin phosphate depending on their concentration, ph of solution, sorbent quantity are obtained. The parameters of extraction of potassium microquantities from sodium salts are defined. Ultra pure sodium chloride, sodium iodide, sodium sulphate, sodium nitrate, sodium nitrite, sodium phosphate are synthesized.

Characterization of Human Bone Alkaline Phosphatase in Pichia Pastoris

Science.gov (United States)

Malone, Christine C.; Ciszak, Eva; Karr, Laurel J.

1999-01-01

A soluble form of human bone alkaline phosphatase has been expressed in a recombinant strain of the methylotrophic yeast Pichia pastoris. We constructed a plasmid containing cDNA encoding for human bone alkaline phosphatase, with the hydrophobic carboxyl terminal portion deleted. Alkaline phosphatase was secreted into the medium to a level of 32mg/L when cultured in shake flasks, and enzyme activity was 12U/mg, as measured by a spectrophotometric assay. By conversion to a fermentation system, a yield of 880mg/L has been achieved with an enzyme activity of 968U/mg. By gel electrophoresis analysis, it appears that greater than 50% of the total protein in the fermentation media is alkaline phosphatase. Although purification procedures are not yet completely optimized, they are expected to include filtration, ion exchange and affinity chromatography. Our presentation will focus on the purification and crystallization results up to the time of the conference. Structural data should provide additional information on the role of alkaline phosphatase in normal bone mineralization and in certain bone mineralization anomalies.

Cyclic, Early Diagenetic Dolomite Formation in Alkaline Lake Van

Science.gov (United States)

McCormack, J.; Bontognali, T. R. R.; Immenhauser, A.; Kwiecien, O.

2017-12-01

Modern dolomite-forming environments are commonly constrained to evaporitic marine or marginal marine settings such as lagoons and sabkhas. Beside microbial mediation, high temperatures and Mg2+ concentrations in solution are factors considered important in aiding dolomite formation. Accordingly, previous studies associate the presence of dolomite within deep sediments of alkaline Lake Van (Turkey) with periods of enhanced evaporation, low lake levels and high Mg/Ca ratio. We systematically studied dolomite within the sedimentary record of Lake Van by means of XRD, SEM and stable isotope (δ18O and δ13C) mass spectrometry. First, we considered the origin of the dolomite; next, we focused on the wider implication of its presence. SEM imaging documents large dolomite crystals interwoven with clay minerals and individual crystals with different crystallographic orientations grown together, indicating space-limited growth within the sediment. According to recent climatic reconstructions for the same sequence (ICDP PALEOVAN project), the water depth of the coring site - today at 350 m - unlikely fell below 200 m. Consequently, dolomite formed below a thick water column at constantly low temperatures (supported by heavy δ18O signature). Within this environment, variations in Mg/Ca ratio, pH and alkalinity, which are constantly high, have no effect on the episodic nature of dolomite precipitation. These observations call for a re-evaluation of the palaeoenvironments often invoked to interpret intervals rich in dolomite within ancient sedimentary sequences (e.g., periods of enhanced aridity and evaporation). Further, and in contrast to previous interpretations, our dolomite concentration data backed up by ICDP PALEOVAN reconstructions suggest that intervals rich in dolomite coincide with periods of high lake level and increased humidity. High dolomite concentrations (20 - 85 % relative carbonate content) occur cyclically within the last glacial period and coincide with

Evolution of the magnesium incorporated amorphous calcium phosphate to nano-crystallized hydroxyapatite in alkaline solution

Science.gov (United States)

Zhang, Xiao-Juan; Lin, Dong-Yang; Yan, Xiao-Hui; Wang, Xiao-Xiang

2011-12-01

A homogeneous amorphous calcium phosphate (ACP) coating containing magnesium was achieved on titanium substrates by electrochemical deposition (ECD). Its amorphous structure is confirmed by transmission electron microscope (TEM) together with grazing reflection absorption infrared spectroscopy (IR) spectrometer. In the images of high-resolution transmission electron microscope (HRTEM), the ACP spheres are assembled by nano-particles with the diameter of 5-10 nm. In the alkaline environment, nucleation of hydroxyapatite (HAP) occurs on the surfaces of ACP spheres. By consuming the Ca and PO 4 ions inside the ACP spheres, the HAP nuclei grow outward. Confirmed by TEM, the ACP spheres converse to hollow HAP spheres composed of HAP nano-needles. The coating is finally constructed by the HAP nano-needles, which are themselves aggregated by numerous nano-particles.

Contemporaneous alkaline and calc-alkaline series in Central Anatolia (Turkey): Spatio-temporal evolution of a post-collisional Quaternary basaltic volcanism

Science.gov (United States)

Dogan-Kulahci, Gullu Deniz; Temel, Abidin; Gourgaud, Alain; Varol, Elif; Guillou, Hervé; Deniel, Catherine

2018-05-01

This study focuses on spatio-temporal evolution of basaltic volcanism in the Central Anatolian post-collisional Quaternary magmatic province which developed along a NE-SW orientation in Turkey. This magmatic province consists of the stratovolcanoes Erciyes (ES) and Hasandag (HS), and the basaltic volcanic fields of Obruk-Zengen (OZ) and Karapınar (KA). The investigated samples range between basic to intermediate in composition (48-56 wt% SiO2), and exhibit calc-alkaline affinity at ES whereas HS, OZ and KA are alkaline in composition. Based on new Ksbnd Ar ages and major element data, the oldest basaltic rock of ES is 1700 ± 40 ka old and exhibits alkaline character, whereas the youngest basaltic trachyandesite is 12 ± 5 ka old and calc-alkaline in composition. Most ES basaltic rocks are younger than 350 ka. All samples dated from HS are alkaline basalts, ranging from 543 ± 12 ka to 2 ± 7 ka old. With the exception of one basalt, all HS basalts are 100 ka or younger in age. Ksbnd Ar ages range from 797 ± 20 ka to 66 ± 7 ka from OZ. All the basalt samples are alkaline in character and are older than the HS alkaline basalts, with the exception of the youngest samples. The oldest and youngest basaltic samples from KA are 280 ± 7 ka and 163 ± 10 ka, respectively, and are calc-alkaline in character. Based on thermobarometric estimates samples from OZ exhibit the highest cpx-liqidus temperature and pressure. For all centers the calculated crystallization depths are between 11 and 28 km and increase from NE to SW. Multistage crystallization in magma chamber(s) located at different depths can explain this range in pressure. Harker variation diagrams coupled with least-squares mass balance calculations support fractional crystallization for ES and, to lesser extend for HS, OZ and KA. All basaltic volcanic rocks of this study are enriched in large-ion lithophile elements (LILE) and light rare earth elements (LREE). The lack of negative anomalies for high field

Pseudomonas syringae evades host Immunity by degrading flagellin monomers with alkaline protease AprA

OpenAIRE

Pel, M.J.C.; Van Dijken, A.J.H.; Bardoel, B.W.; Seidl, M.F; Van der Ent, S.; Van Strijp, J.A.G.

2014-01-01

Bacterial flagellin molecules are strong inducers of innate immune responses in both mammals and plants. The opportunistic pathogen Pseudomonas aeruginosa secretes an alkaline protease called AprA that degrades flagellin monomers. Here, we show that AprA is widespread among a wide variety of bacterial species. In addition, we investigated the role of AprA in virulence of the bacterial plant athogen P. syringae pv. tomato DC3000. The AprA-deficient DC3000 ΔaprA knockout mutant was significantl...

Development of Effective Solvent Modifiers for the Solvent Extraction of Cesium from Alkaline High-Level Tank Waste

International Nuclear Information System (INIS)

Bonnesen, Peter V.; Delmau, Laetitia H.; Moyer, Bruce A.; Lumetta, Gregg J.

2003-01-01

A series of novel alkylphenoxy fluorinated alcohols were prepared and investigated for their effectiveness as modifiers in solvents containing calix(4)arene-bis-(tert-octylbenzo)-crown-6 for extracting cesium from alkaline nitrate media. A modifier that contained a terminal 1,1,2,2-tetrafluoroethoxy group was found to decompose following long-term exposure to warm alkaline solutions. However, replacement of the tetrafluoroethoxy group with a 2,2,3,3-tetrafluoropropoxy group led to a series of modifiers that possessed the alkaline stability required for a solvent extraction process. Within this series of modifiers, the structure of the alkyl substituent (tert-octyl, tert-butyl, tert-amyl, and sec-butyl) of the alkylphenoxy moiety was found to have a profound impact on the phase behavior of the solvent in liquid-liquid contacting experiments, and hence on the overall suitability of the modifier for a solvent extraction process. The sec-butyl derivative(1-(2,2,3,3-tetrafluoropropoxy)-3- (4-sec-butylphenoxy)-2-propanol) (Cs-7SB) was found to possess the best overall balance of properties with respect to third phase and coalescence behavior, cleanup following degradation, resistance to solids formation, and cesium distribution behavior. Accordingly, this modifier was selected for use as a component of the solvent employed in the Caustic-Side Solvent Extraction (CSSX) process for removing cesium from high level nuclear waste (HLW) at the U.S. Department of Energy's (DOE) Savannah River Site. In batch equilibrium experiments, this solvent has also been successfully shown to extract cesium from both simulated and actual solutions generated from caustic leaching of HLW tank sludge stored in tank B-110 at the DOE's Hanford Site.

Mineral Element Concentrations in Vegetables Cultivated in Acidic Compared to Alkaline Areas of South Sweden

Directory of Open Access Journals (Sweden)

Ingegerd Rosborg

2009-01-01

Full Text Available A study in 1997, on mineral levels in acidic compared to alkaline well waters, and in women’s hair, revealed higher concentrations of a number of mineral elements like Ca, Mo and Se in alkaline waters and hair. Thus, median Ca levels were six times higher in well water and five times higher in hair from the alkaline area compared to the acidic area. This finding raised the probability of similar differences in vegetables from these areas. Thus, in the year 2006, 60 women who had participated in the study in 1997 were asked to cultivate parsley, lettuce, carrot and chive. During the spring of 2006, the women from the water and hair study of 1997, 30 of them from the acidic area and 30 women from the alkaline district cultivated vegetables: carrot (Daucus carota L, parsley (Petroselinum crispum, chive (Allium schoenoprasum and lettuce (Eruca sativa. The vegetables were harvested, and rinsed in tap water from the kitchens of the participating women in August. The concentrations of about 35 elements and ions were determined by ICP OES and ICP-MS predominantly. In addition, soil samples from the different cultivators were also analyzed for a number of elements. Lettuce and parsley showed the highest concentrations of mineral elements per gram dry weight. Only Mo concentrations were significantly higher in all the different vegetables from the alkaline district compared to vegetables from the acidic areas. On the other hand, the concentrations of Ba, Br, Mn, Rb and Zn were higher in all the different vegetables from the acidic area. In the soil, only pH and exchangeable Ca from the alkaline area were higher than from the acidic area, while exchangeable Fe, Mn and Na concentrations were higher in soils from the acidic area. Soil elements like Al, Fe, Li, Ni, Pb, Si, Ti, V, Zn and Zr were found in higher concentrations in lettuce and parsley, which were attributed to soil particles being splashed on the plants by the rain and absorbed by the leaves

Characterization of an anionic-exchange membranes for direct methanol alkaline fuel cells

Energy Technology Data Exchange (ETDEWEB)

Abuin, Graciela C. [Centro de Procesos Superficiales, Instituto Nacional de Tecnologia Industrial (INTI), Av. Gral. Paz 5445, B1650KNA, San Martin, Buenos Aires (Argentina); Nonjola, Patrick; Mathe, Mkhulu K. [Council for Scientific and Industrial Research (CSIR), Material Science and Manufacturing, PO Box 395, Brumeria, Pretoria 0001 (South Africa); Franceschini, Esteban A.; Izraelevitch, Federico H.; Corti, Horacio R. [Departamento de Fisica de la Materia Condensada, Comision Nacional de Energia Atomica (CNEA), Av. Gral. Paz 1499, B1650KNA, San Martin, Buenos Aires (Argentina)

2010-06-15

Ammonium quaternized polymers such as poly (arylene ether sulfones) are being developed and studied as candidates of ionomeric materials for application in alkaline fuel cells, due to their low cost and promising electrochemical properties. In this work, a quaternary ammonium polymer was synthesized by chloromethylation of a commercial polysulfone followed by amination process. Quaternized polysulfone membrane properties such us water and water-methanol uptake, electrical conductivity and Young's modulus were evaluated and compared to Nafion 117, commonly employed in direct methanol fuel cells. The anionic polysulfone membrane sorbs more water than Nafion all over the whole range of water activities, but it uptakes much less methanol as compared to Nafion. The specific conductivity of the fully hydrated polysulfone membrane equilibrated with KOH solutions at ambient temperature increases with the KOH concentration, reaching a maximum of 0.083 S cm{sup -1} for 2 M KOH, slightly less conductive than Nafion 117. The elastic modulus of the polysulfone membranes inmersed in water is similar to that reported for Nafion membranes under the same conditions. We concluded that quaternized polysulfone membrane are good candidates as electrolytes in alkaline direct methanol fuel cells. (author)

Structural analysis of alkaline β-mannanase from alkaliphilic Bacillus sp. N16-5: implications for adaptation to alkaline conditions.

Directory of Open Access Journals (Sweden)

Yueju Zhao

Full Text Available Significant progress has been made in isolating novel alkaline β-mannanases, however, there is a paucity of information concerning the structural basis for alkaline tolerance displayed by these β-mannanases. We report the catalytic domain structure of an industrially important β-mannanase from the alkaliphilic Bacillus sp. N16-5 (BSP165 MAN at a resolution of 1.6 Å. This enzyme, classified into subfamily 8 in glycosyl hydrolase family 5 (GH5, has a pH optimum of enzymatic activity at pH 9.5 and folds into a classic (β/α(8-barrel. In order to gain insight into molecular features for alkaline adaptation, we compared BSP165 MAN with previously reported GH5 β-mannanases. It was revealed that BSP165 MAN and other subfamily 8 β-mannanases have significantly increased hydrophobic and Arg residues content and decreased polar residues, comparing to β-mannanases of subfamily 7 or 10 in GH5 which display optimum activities at lower pH. Further, extensive structural comparisons show alkaline β-mannanases possess a set of distinctive features. Position and length of some helices, strands and loops of the TIM barrel structures are changed, which contributes, to a certain degree, to the distinctly different shaped (β/α(8-barrels, thus affecting the catalytic environment of these enzymes. The number of negatively charged residues is increased on the molecular surface, and fewer polar residues are exposed to the solvent. Two amino acid substitutions in the vicinity of the acid/base catalyst were proposed to be possibly responsible for the variation in pH optimum of these homologous enzymes in subfamily 8 of GH5, identified by sequence homology analysis and pK(a calculations of the active site residues. Mutational analysis has proved that Gln91 and Glu226 are important for BSP165 MAN to function at high pH. These findings are proposed to be possible factors implicated in the alkaline adaptation of GH5 β-mannanases and will help to further

Osteocalcin and bone-specific alkaline phosphatase in Sickle cell ...

African Journals Online (AJOL)

specific alkaline phosphatase (b-AP) total protein levels were evaluated as indicators of bone turnover in twenty patients with sickle cell haemoglobinopathies and in twenty normal healthy individuals. The serum bonespecific alkaline phosphatase ...

Chemical degradation of fluoroelastomer in an alkaline environment

DEFF Research Database (Denmark)

Mitra, S.; Ghanbari-Siahkali, A.; Kingshott, P.

2004-01-01

We have investigated the time-dependent chemical degradation of a fluoroelastomer, FKM (Viton((R)) A), in an alkaline environment (10% NaOH, 80 degreesC). Optical microscopy and SEM analysis reveal that degradation starts with surface roughness right from the earliest stage of exposure (e.g., 1...... week) and finally results in cracks on the surface after prolonged exposure. Initially the extent of degradation is mainly confined to the surface regions (a few nanometers) but with longer exposure (e.g., 12 weeks) it extends to below the subsurface region of the fluoroelastomer. The extent...... of this surface degradation is found to be strong enough to affect the bulk mechanical properties. The molecular mechanisms of the surface chemical degradation were determined using surface analysis (XPS and ATR-FTIR) where the initial degradation was found to proceed via dehydrofluorination. This leads to double...

IUPAC-NIST Solubility Data Series. 95. Alkaline Earth Carbonates in Aqueous Systems. Part 2. Ca

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