Extensive Gustatory Cortex Lesions Significantly Impair Taste Sensitivity to KCl and Quinine but Not to Sucrose in Rats.

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Michelle B Bales

Full Text Available Recently, we reported that large bilateral gustatory cortex (GC lesions significantly impair taste sensitivity to salts in rats. Here we extended the tastants examined to include sucrose and quinine in rats with ibotenic acid-induced lesions in GC (GCX and in sham-operated controls (SHAM. Presurgically, immediately after drinking NaCl, rats received a LiCl or saline injection (i.p., but postsurgical tests indicated a weak conditioned taste aversion (CTA even in controls. The rats were then trained and tested in gustometers to discriminate a tastant from water in a two-response operant taste detection task. Psychometric functions were derived for sucrose, KCl, and quinine. Our mapping system was used to determine placement, size, and symmetry of the lesions (~91% GC damage on average. For KCl, there was a significant rightward shift (ΔEC50 = 0.57 log10 units; p<0.001 in the GCX psychometric function relative to SHAM, replicating our prior work. There was also a significant lesion-induced impairment (ΔEC50 = 0.41 log10 units; p = 0.006 in quinine sensitivity. Surprisingly, taste sensitivity to sucrose was unaffected by the extensive lesions and was comparable between GCX and SHAM rats. The fact that such large bilateral GC lesions did not shift sucrose psychometric functions relative to SHAM, but did significantly compromise quinine and KCl sensitivity suggests that the neural circuits responsible for the detection of specific taste stimuli are partially dissociable. Lesion-induced impairments were observed in expression of a postsurgical CTA to a maltodextrin solution as assessed in a taste-oriented brief-access test, but were not reflected in a longer term 46-h two-bottle test. Thus, deficits observed in rats after extensive damage to the GC are also dependent on the test used to assess taste function. In conclusion, the degree to which the GC is necessary for the maintenance of normal taste detectability apparently depends on the chemical and

Co adaptation of LiCl tolerant Solanum tuberosum L. callus cultures ...

African Journals Online (AJOL)

Jane

2011-10-12

Oct 12, 2011 ... also brings about tolerance to osmotic effects of salt. This data is highly .... These RGR values of control and LiCl adapted calli were used as reference .... by the Higher Education Commission (HEC) grants. The technical ...

Terahertz reflection spectroscopy of aqueous NaCl and LiCl solutions

DEFF Research Database (Denmark)

Jepsen, Peter Uhd; Merbold, Hannes

2010-01-01

frequencies. Whereas both the real and imaginary part of the permittivity of NaCl increases with concentration,we see that the imaginary part of the permittivity of LiCl (related to the absorption)decreases with increasing salt concentration. We relate these changes to the behavior...

Inversion of the calcium isotope separation at an ion exchanger resin by variation of the LiCl electrolyte concentration

International Nuclear Information System (INIS)

Heumann, K.G.; Kloeppel, H.; Sigl, G.

1982-01-01

The calcium isotope separation at a strongly acidic exchanger resin as a function of the concentration of a LiCl solution is investigated in column experiments. Whereas an enrichment of the heavier calcium isotopes in the solution phase is found with a 3 M LiCl solution, an inverse effect is obtained with 8 M and 12 M LiCl solutions. The separation effect epsilon for the 12 M solution is found to be the highest calcium enrichment in a system without a complexing agent. The results are compared with those for other electrolyte solutions and can be explained by the anion/cation interactions. (orig.)

Growth inhibitor of E. coli K-12 in a sample of 39KCl

International Nuclear Information System (INIS)

Luckey, T.D.

1984-01-01

Growth rates and total population of E. coli were reduced fourfold when natural KCl (/sup N/KCl) in the medium was replaced by 39 KCl from a particular source. A prolonged lag period was noted in cultures containing either /sup N/KCl or 39 KCl when inoculated with bacteria adapted to 39 KCl. These changes were not due to endogenous radiation because these differences were not observed when (a) the KCl concentrations were reduced from 50 to 5 mM and (b) the 39 KCl from the prime source was replaced with 39 KCl from a second source; also the addition of 40 KCl to 39 KCl did not improve growth. These results suggest that the 39 KCl from the primary source contained an unidentified inhibitor that is not readily detected by physical and chemical analyses. 8 references, 3 figures, 2 tables

High density liquid structure enhancement in glass forming aqueous solution of LiCl

Science.gov (United States)

Camisasca, G.; De Marzio, M.; Rovere, M.; Gallo, P.

2018-06-01

We investigate using molecular dynamics simulations the dynamical and structural properties of LiCl:6H2O aqueous solution upon supercooling. This ionic solution is a glass forming liquid of relevant interest in connection with the study of the anomalies of supercooled water. The LiCl:6H2O solution is easily supercooled and the liquid state can be maintained over a large decreasing temperature range. We performed simulations from ambient to 200 K in order to investigate how the presence of the salt modifies the behavior of supercooled water. The study of the relaxation time of the self-density correlation function shows that the system follows the prediction of the mode coupling theory and behaves like a fragile liquid in all the range explored. The analysis of the changes in the water structure induced by the salt shows that while the salt preserves the water hydrogen bonds in the system, it strongly affects the tetrahedral hydrogen bond network. Following the interpretation of the anomalies of water in terms of a two-state model, the modifications of the oxygen radial distribution function and the angular distribution function of the hydrogen bonds in water indicate that LiCl has the role of enhancing the high density liquid component of water with respect to the low density component. This is in agreement with recent experiments on aqueous ionic solutions.

The taste of KCl - What a difference a sugar makes.

Science.gov (United States)

Ben Abu, Natalie; Harries, Daniel; Voet, Hillary; Niv, Masha Y

2018-07-30

Dramatic increase in NaCl consumption lead to sodium intake beyond health guidelines. KCl substitution helps reduce sodium intake but results in a bitter-metallic off-taste. Two disaccharides, trehalose and sucrose, were tested in order to untangle the chemical (increase in effective concentration of KCl due to sugar addition) from the sensory effects. The bitter-metallic taste of KCl was reduced by these sugars, while saltiness was enhanced or unaltered. The perceived sweetness of sugar, regardless of its type and concentration, was an important factor in KCl taste modulation. Though KCl was previously shown to increase the chemical activity of trehalose but not of sucrose, we found that it suppressed the perceived sweetness of both sugars. Therefore, sensory integration was the dominant factor in the tested KCl-sugar combinations. Copyright © 2018 Elsevier Ltd. All rights reserved.

Molten salt synthesis of La0.8Sr0.2MnO3 powders for SOFC cathode electrode

Science.gov (United States)

Gu, Sin-il; Shin, Hyo-soon; Hong, Youn-woo; Yeo, Dong-hun; Kim, Jong-hee; Nahm, Sahn; Yoon, Sang-ok

2012-08-01

For La0.8Sr0.2MnO3 (LSM) perovskite, used as the cathode material for solid oxide fuel cells (SOFC), it is known that the formation of a triple-phase-boundary is restrained due to the formation of a second phase at the YSZ/electrode interface at high temperature. To decrease the 2nd phase, lowering the sintering temperature has been used. LSM powder was synthesized by molten salt synthesis method to control its particle size, shape, and agglomeration. We have characterized the phase formation, particle size, shape, and sintering behavior of LSM in the synthesis using the variation of KCl, LiCl, KF and its mixed salts as raw materials. In the case of KCl and KCl-KF salts, the particle size and shape of the LSM was well controlled and synthesized. However, in the case of LiCl and KCl-LiCl salts, LiMnOx as 2nd phase and LSM were synthesized simultaneously. In the case of the mixed salt of KCl-KF, the growth mechanism of the LSM particle was changed from `diffusion-controlled' to `reaction-controlled' according to the amount of mixed salt. The sintering temperature can be decreased below 1000 °C by using the synthesized LSM powder.

KCl stimulation increases norepinephrine transporter function in PC12 cells.

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Mandela, Prashant; Ordway, Gregory A

2006-09-01

The norepinephrine transporter (NET) plays a pivotal role in terminating noradrenergic signaling and conserving norepinephrine (NE) through the process of re-uptake. Recent evidence suggests a close association between NE release and regulation of NET function. The present study evaluated the relationship between release and uptake, and the cellular mechanisms that govern these processes. KCl stimulation of PC12 cells robustly increased [3H]NE uptake via the NET and simultaneously increased [3H]NE release. KCl-stimulated increases in uptake and release were dependent on Ca2+. Treatment of cells with phorbol-12-myristate-13-acetate (PMA) or okadaic acid decreased [3H]NE uptake but did not block KCl-stimulated increases in [3H]NE uptake. In contrast, PMA increased [3H]NE release and augmented KCl-stimulated release, while okadaic acid had no effects on release. Inhibition of Ca2+-activated signaling cascades with KN93 (a Ca2+ calmodulin-dependent kinase inhibitor), or ML7 and ML9 (myosin light chain kinase inhibitors), reduced [3H]NE uptake and blocked KCl-stimulated increases in uptake. In contrast, KN93, ML7 and ML9 had no effect on KCl-stimulated [3H]NE release. KCl-stimulated increases in [3H]NE uptake were independent of transporter trafficking to the plasma membrane. While increases in both NE release and uptake mediated by KCl stimulation require Ca2+, different intracellular mechanisms mediate these two events.

Volatility of components of saturated vapours of UCl4-CsCl and UCl4-LiCl molten mixtures

International Nuclear Information System (INIS)

Smirnov, M.V.; Kudyakov, V.Ya.; Salyulev, A.B.; Komarov, V.E.; Posokhin, Yu.V.; Afonichkin, V.K.

1979-01-01

The flow method has been used for measuring the volatility of the components from UCl 4 -CsCl and UCl 4 -LiCl melted mixtures containing 2.0, 5.0, 12.0, 25.0, 33.0, 50.0, 67.0, and 83.0 mol.% of UCl 4 within the temperature ranges of 903-1188 K and 740-1200 K, respectively. The chemical composition of saturated vapours above the melted salts has been determined. The melted mixtures in question exhibit negative deviation from ideal behaviour. Made was the conclusion about the presence in a vapour phase, along with monomeric UCl 4 , LiCl, CsCl and Li 2 Cl 2 , Cs 2 Cl 2 dimers of double compounds of the MeUCl 5 most probable composition. Their absolute contribution into a total pressure above the UCl 4 -CsCl melted mixtures is considerably smaller than above the UCl 4 -LiCl mixtures

Lithium isotope effect during solvent extraction of LiCl with isoamyl alcohol

International Nuclear Information System (INIS)

Levkin, A.V.; Zhilov, V.I.; Marokin, O.V.; Demin, S.V.

1991-01-01

Method of extraction chromatography was used to measure the coefficient of lithium isotope separation (α) during extraction with isoamyl alcohol from concentrated LiCl aqueous solution. The α value is equal to 1.0036±0.0009; heavy 7 Li isotope is concentrated in organic phase at that

IRSL characteristics of NaCl and KCl relative to dosimeter

International Nuclear Information System (INIS)

Tanir, Guenes; Hicabi Boeluekdemir, M.; Catli, Serap; Tel, Eyyuep

2007-01-01

The aim of this work is to determine and compare the dosimetric properties of NaCl and KCl samples using infrared-stimulated luminescence (IRSL) technique. For a material to be used as dosimeter, both the IRSL temperature dependence and the radiation dose response have critical importance. In this work the IRSL characteristics from NaCl and KCl samples were experimentally investigated as a function of temperature and laboratory radiation doses. Dosimetric properties of NaCl and KCl samples were found significantly different. The IRSL signals displayed by NaCl were found to be more stable, reliable and agreeable than those of KCl

Growth and time dependent alignment of KCl crystals in Hemoglobin LB monolayer

International Nuclear Information System (INIS)

Mahato, Mrityunjoy; Pal, Prabir; Tah, Bidisha; Kamilya, Tapanendu; Talapatra, G.B.

2012-01-01

Nature and organism often use the biomineralization technique to build up various highly regular structures such as bone, teeth, kidney stone etc., and recently this becomes the strategy to design and synthesis of novel biocomposite materials. We report here the controlled crystallization of KCl in Langmuir and Langmuir Blodgett (LB) monolayer of Hemoglobin (Hb) at ambient condition. The nucleation and growth of KCl crystals in Hb monolayer has temporal and KCl concentration dependency. The growth of KCl crystals in LB film of Hb has distinct behavior in the alignment of crystals from linear to fractal like structures depending on growth time. The crystallographic identity of the biomineralized KCl crystal is confirmed from HR-TEM, XRD, and from powder diffraction simulation. Our results substantiated that the template of Langmuir monolayer of proteins plays a crucial role in biomineralization as well as in designing and synthesizing of novel biocomposite materials. Highlights: ► Biomineralization of KCl crystal has been studied in Hemoglobin LB film. ► KCl crystal growth is time and concentration of KCl dependent. ► The alignment of KCl crystal growth is fractal nature with time. ► The unfolding of Hb and evaporation factor has some role in crystallization and fractal growth.

New colour centres in KCl:(Tl+ + Ca2+) and KCl:(Tl+ + Sr2+) crystals

International Nuclear Information System (INIS)

Ioan, A.; Topa, V.; Giurgea, M.

1978-01-01

Electrolytic colouring under unusual conditions (low temperature and high voltage) gives rise to the appearance of three new absorption bands peaking at 3.2, 2.5, and 1.7 eV and at 2.8, 2.1, and 1.5 eV in KCl:(Tl + + Ca 2+ ) and in KCl:(Tl + + Sr 2+ ) single crystals, respectively. The modifications of the absorption spectra of the coloured crystals induced by the application of a reversed electric field at the colouring temperature or by heat treatment are investigated. It is likely that the colour centre responsible for the new absorption bands is an aggregate centre which, besides an Tl - -complex, contains also at least an Ca(Sr) ion, a trapped electron, and an anionic vacancy. (author)

Stabilization of molten salt materials using metal chlorides for solar thermal storage.

Science.gov (United States)

Dunlop, T O; Jarvis, D J; Voice, W E; Sullivan, J H

2018-05-29

The effect of a variety of metal-chlorides additions on the melting behavior and thermal stability of commercially available salts was investigated. Ternary salts comprised of KNO 3, NaNO 2, and NaNO 3 were produced with additions of a variety of chlorides (KCl, LiCl, CaCl 2 , ZnCl 2 , NaCl and MgCl 2 ). Thermogravimetric analysis and weight loss experiments showed that the quaternary salt containing a 5 wt% addition of LiCl and KCl led to an increase in short term thermal stability compared to the ternary control salts. These additions allowed the salts to remain stable up to a temperature of 630 °C. Long term weight loss experiments showed an upper stability increase of 50 °C. A 5 wt% LiCl addition resulted in a weight loss of only 25% after 30 hours in comparison to a 61% loss for control ternary salts. Calorimetry showed that LiCl additions allow partial melting at 80 °C, in comparison to the 142 °C of ternary salts. This drop in melting point, combined with increased stability, provided a molten working range increase of almost 100 °C in total, in comparison to the control ternary salts. XRD analysis showed the oxidation effect of decomposing salts and the additional phase created with LiCl additions to allow melting point changes to occur.

Platelet-derived growth factor regulates K-Cl cotransport in vascular smooth muscle cells.

Science.gov (United States)

Zhang, Jing; Lauf, Peter K; Adragna, Norma C

2003-03-01

Platelet-derived growth factor (PDGF), a potent serum mitogen for vascular smooth muscle cells (VSMCs), plays an important role in membrane transport regulation and in atherosclerosis. K-Cl cotransport (K-Cl COT/KCC), the coupled-movement of K and Cl, is involved in ion homeostasis. VSMCs possess K-Cl COT activity and the KCC1 and KCC3 isoforms. Here, we report on the effect of PDGF on K-Cl COT activity and mRNA expression in primary cultures of rat VSMCs. K-Cl COT was determined as the Cl-dependent Rb influx and mRNA expression by semiquantitative RT-PCR. Twenty four-hour serum deprivation inhibited basal K-Cl COT activity. Addition of PDGF increased total protein content and K-Cl COT activity in a time-dependent manner. PDGF activated K-Cl COT in a dose-dependent manner, both acutely (10 min) and chronically (12 h). AG-1296, a selective inhibitor of the PDGF receptor tyrosine kinase, abolished these effects. Actinomycin D and cycloheximide had no effect on the acute PDGF activation of K-Cl COT, suggesting posttranslational regulation by the drug. Furthermore, PDGF increased KCC1 and decreased KCC3 mRNA expression in a time-dependent manner. These results indicate that chronic activation of K-Cl COT activity by PDGF may involve regulation of the two KCC mRNA isoforms, with KCC1 playing a dominant role in the mechanism of PDGF-mediated activation.

KCl cotransport regulation and protein kinase G in cultured vascular smooth muscle cells.

Science.gov (United States)

Adragna, N C; Zhang, J; Di Fulvio, M; Lincoln, T M; Lauf, P K

2002-05-15

K-Cl cotransport is activated by vasodilators in erythrocytes and vascular smooth muscle cells and its regulation involves putative kinase/phosphatase cascades. N-ethylmaleimide (NEM) activates the system presumably by inhibiting a protein kinase. Nitrovasodilators relax smooth muscle via cGMP-dependent activation of protein kinase G (PKG), a regulator of membrane channels and transporters. We investigated whether PKG regulates K-Cl cotransport activity or mRNA expression in normal, PKG-deficient-vector-only-transfected (PKG-) and PKG-catalytic-domain-transfected (PKG+) rat aortic smooth muscle cells. K-Cl cotransport was calculated as the Cl-dependent Rb influx, and mRNA was determined by semiquantitative RT-PCR. Baseline K-Cl cotransport was higher in PKG+ than in PKG- cells (p <0.01). At 0.5 mM, NEM stimulated K-Cl cotransport by 5-fold in PKG- but not in PKG+ cells. However, NEM was more potent although less effective to activate K-Cl cotransport in normal (passage 1-3) and PKG+ than in PKG- cells. In PKG- cells, [(dihydroindenyl) oxy] alkanoic acid (300 mM) but not furosemide (1 mM) inhibited K-Cl cotransport. Furthermore, no difference in K-Cl cotransport mRNA expression was observed between these cells. In conclusion, this study shows that manipulation of PKG expression in vascular smooth muscle cells affects K-Cl cotransport activity and its activation by NEM.

Volatility of components of saturated vapours of UCl/sub 4/-CsCl and UCl/sub 4/-LiCl molten mixtures

Energy Technology Data Exchange (ETDEWEB)

Smirnov, M V; Kudyakov, V Ya; Salyulev, A B; Komarov, V E; Posokhin, Yu V; Afonichkin, V K

1979-01-01

The flow method has been used for measuring the volatility of the components from UCl/sub 4/-CsCl and UCl/sub 4/-LiCl melted mixtures containing 2.0, 5.0, 12.0, 25.0, 33.0, 50.0, 67.0, and 83.0 mol.% of UCl/sub 4/ within the temperature ranges of 903-1188 K and 740-1200 K, respectively. The chemical composition of saturated vapours above the melted salts has been determined. The melted mixtures in question exhibit negative deviation from ideal behaviour. Made was the conclusion about the presence in a vapour phase, along with monomeric UCl/sub 4/, LiCl, CsCl and Li/sub 2/Cl/sub 2/, Cs/sub 2/Cl/sub 2/ dimers of double compounds of the MeUCl/sub 5/ most probable composition. Their absolute contribution into a total pressure above the UCl/sub 4/-CsCl melted mixtures is considerably smaller than above the UCl/sub 4/ -LiCl mixtures.

Meltability in system of K2TaF7-NaF-NaCl-KCl

International Nuclear Information System (INIS)

Kartsev, V.E.; Kovalev, F.V.; Korshunov, B.G.

1975-01-01

Thermographic and visual-polythermal techniques were used to study the meltability in K 2 TaF 7 -NaF-NaCl-KCl system. The tetrahedron-forming sections NaF-NaCl-K 2 TaF 7 xKCl and NaF-K 2 TaF 7 xKCl-2K 2 TaF 7 xNaCl divide the concentration tetrahedron into three particular tetrahedra: NaF-K 2 TaF 7 xKCl-2K 2 TaF 7 xNaCl-K 2 TaF 7 , NaF-NaCl-K 2 TaF 7 xKCl-2K 2 TaF 7 xaCl, and NaF-NaCl-KCl-K 2 TaF 7 xKCl. Non-variant equilibrium points in all of the particular four-component systems have been determined

Mechanism of norepinephrine release elicited by renal nerve stimulation, veratridine and potassium chloride in the isolated rat kidney

International Nuclear Information System (INIS)

el-Din, M.M.; Malik, K.U.

1987-01-01

We have investigated the mechanism by which renal nerve stimulation (RNS), veratridine (Vt) and KCl promote release of norepinephrine in the isolated rat kidney perfused with Tyrode's solution and prelabeled with [ 3 H]norepinephrine by examining the overflow of tritium elicited by these stimuli during 1) extracellular Ca++ depletion, 2) alterations in extracellular Na+ concentration and 3) administration of tetrodotoxin, amiloride, LiCl and calcium channel blockers. RNS (1-4 Hz), Vt (15-90 nmol) and KCl (150-500 mumol) produced renal vasoconstriction and enhanced the tritium overflow in a frequency- and concentration-dependent manner, respectively. Omission of Ca++ (1.8 mM) from the perfusion fluid abolished the renal vasoconstriction and the increase in tritium overflow elicited by RNA and KCl and substantially reduced that caused by Vt. Lowering the Na+ concentration in the perfusion medium (from 150 to 25 mM) reduced the overflow of tritium and the renal vasoconstriction caused by RNS (2 Hz) or Vt (45 nmol); the increase in tritium overflow in response to these stimuli was positively correlated with extracellular Na+ (25-150 mM). In contrast, KCl-induced tritium overflow was negatively correlated with extracellular Na+ concentration. Tetrodotoxin (0.3 microM) abolished the effect of RNS and Vt, but not that of KCl, to increase overflow of tritium and to produce renal vasoconstriction. Administration of amiloride (180 microM) enhanced the overflow of tritium but attenuated the associated renal vasoconstriction produced by RNS, Vt and KCl. Replacement of NaCl (75 mM) with equimolar concentration of LiCl enhanced the overflow of tritium elicited by RNS, Vt and KCl; the associated renal vasoconstriction remained unaltered

Effect of Sr2+ concentration on generation of colour centres in KCl crystals

International Nuclear Information System (INIS)

Kowalczyk, J.; Damm, J.Z.

1976-01-01

Gamma radiation induced generation of F- and V-type colour centres in KCl crystals (one pure and eight Sr-doped) is examined. Beginning with about 66 ppm Sr in the sample the late colouration stage is practically suppressed. It is shown that V 2 bands are characteristic for the initial colouration stage and V 3 band for the late colouration stage. The latter band appears in the pure or low-doped KCl and in plastically deformed high-doped KCl. The introduction of fresh dislocation into the crystal either by irradiation (low-doped KCl) or by plastic deformation (high-doped KCl) is responsible for the disappearance of primary cation vacancies. Some additional data concerning the dose-rate effect and generation of F 2 (M) centres are presented. (author)

The effect of NaCl substitution by KCl on telemea cheese properties

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Mihai ANGHELOIU

2016-12-01

Full Text Available The effect of partial or total substitution of sodium chloride by potassium chloride on the chemical composition, texture profile and sensory properties of Telemea cheese during 28 days of ripening at 4°C was evaluated in the current study. Telemea cheese was ripened in 4 different brine solutions (20%, wt/wt made from different NaCl:KCl ratios as follows: (NaCl (A, KCl (B, 1NaCl:1KCl (C and 1NaCl:2KCl (D. The physicochemical properties of Telemea cheese (dry matter, fat, protein, ash, pH, total nitrogen (TN, water soluble nitrogen (WSN and ripening degree values were determined after 1, 7, 14, 21 and 28 days of ripening. Dry matter, pH and ripening degree values were significantly (p < 0.05 affected during ripening. The results of this study indicated that replacing 66% NaCl with KCl influenced the texture profile and sensorial characteristics of Telemea cheese.

Optical investigation of gas-phase KCl/KOH sulfation in post flame conditions

DEFF Research Database (Denmark)

Weng, Wubin; chen, Shuang; Wu, Hao

2018-01-01

A counter-flow reactor setup was designed to investigate the gas-phase sulfation and homogeneous nucleation of potassium salts. Gaseous KOH and KCl were introduced into the post-flame zone of a laminar flat flame. The hot flame products mixed in the counter-flow with cold N2, with or without....... Depending on the potassium speciation in the inlet and the presence of SO2, they consisted of K2SO4, KCl, or K2CO3, respectively. The experiments showed that KOH was sulphated more readily than KCl, resulting in larger quantities of aerosols. The sulfation process in the counter-flow setup was simulated...... using a chemical kinetic model including a detailed subset for the Cl/S/K chemistry. Similar to the experimental results, much more potassium sulfate was predicted when seeding KOH compared to seeding KCl. For both KOH and KCl, sulfation was predicted to occur primarily through the reactions among...

Hydrothermal growth of ZnO nanorods: The role of KCl in controlling rod morphology

International Nuclear Information System (INIS)

Downing, Jonathan M.; Ryan, Mary P.; McLachlan, Martyn A.

2013-01-01

The role of potassium chloride (KCl) in controlling ZnO nanorod morphology of large area thin films prepared by hydrothermal growth has been extensively investigated. The influence of KCl and growth time on the orientation, morphology and microstructure of the nanorod arrays has been studied with systematic changes in the length, width, density and termination of the nanorods observed. Such changes are attributed to stabilization of the high-energy (002) nanorod surface by the KCl. At low KCl concentrations (< 100 mM) c-axis growth i.e. perpendicular to the polar surface, dominates, leading to nanorods with increased length over the control sample (0 mM KCl). At higher concentrations (> 100 mM) stabilization of the high-energy surface by KCl occurs and planar (002) facets are observed accompanied by increased lateral (100) growth, at the highest KCl concentrations near coalesced (002) terminated rods are observed. Additionally we correlate the KCl concentration with the uniformity of the nanorod arrays; a decrease in polydispersity with increased KCl concentration is observed. The vertical alignment of nanorod arrays was studied using X-ray diffraction, it was found that this parameter increases as growth time and KCl concentration are increased. We propose that the increase in vertical alignment is a result of nanorod–nanorod interactions during the early stages of growth. - Highlights: • Modified hydrothermal growth was used for controlled ZnO nanorod synthesis. • Growth conditions varied to study influence on nanorod morphology and orientation. • A highly controlled and reproducible method is established. • A mechanism for growth and the role of ionic additives is proposed

Creation of radiation defects in KCl crystals

International Nuclear Information System (INIS)

Lushchik, A.Ch.; Pung, L.A.; Khaldre, Yu.Yu.; Kolk, Yu.V.

1981-01-01

Optical and EPR methods were used to study the creation of anion and cation Frenkel defects in KCl crystals irradiated by X-ray and VUV-radiation. The decay of excitons with the creation of charged Frenkel defects (α and I centres) was detected and investigated at 4.2 K. The decay of excitons as well as the recombination of electrons with self-trapped holes leads to the creation of neutral Frenkel defects (F and H centres). The creation of Cl 3 - and Vsub(F) centres (cation vacancy is a component of these centres) by X-irradiation at 80 K proves the possibility of cation defects creation in KCl [ru

Phase transition of KCl under shock compression

CERN Document Server

Mashimo, T; Tsumoto, K; Zhang, Y; Ando, S; Tonda, H

2002-01-01

It had been reported that for potassium chloride (KCl) the B1-B2 phase transition (PT) occurs under shock and static compressions, but the measured transition points showed large scatter. In this study, Hugoniot measurement experiments were performed on KCl single crystals by the inclined-mirror method combined with use of a powder gun. The anisotropic Hugoniot elastic limits and PT points were observed. The PT points along the (100), (110) and (111) axis directions were determined as 2.5, 2.2 and 2.1 GPa, respectively. The anisotropic transition was reasonably explained in terms of the displacement mechanism along the (111) axis direction.

Signal transduction mechanisms of K+-Cl- cotransport regulation and relationship to disease.

Science.gov (United States)

Adragna, N C; Ferrell, C M; Zhang, J; Di Fulvio, M; Temprana, C F; Sharma, A; Fyffe, R E W; Cool, D R; Lauf, P K

2006-01-01

The K+-Cl- cotransport (COT) regulatory pathways recently uncovered in our laboratory and their implication in disease state are reviewed. Three mechanisms of K+-Cl- COT regulation can be identified in vascular cells: (1) the Li+-sensitive pathway, (2) the platelet-derived growth factor (PDGF)-sensitive pathway and (3) the nitric oxide (NO)-dependent pathway. Ion fluxes, Western blotting, semi-quantitative RT-PCR, immunofluorescence and confocal microscopy were used. Li+, used in the treatment of manic depression, stimulates volume-sensitive K+-Cl- COT of low K+ sheep red blood cells at cellular concentrations 3 mM, causes cell swelling, and appears to regulate K+-Cl- COT through a protein kinase C-dependent pathway. PDGF, a potent serum mitogen for vascular smooth muscle cells (VSMCs), regulates membrane transport and is involved in atherosclerosis. PDGF stimulates VSM K+-Cl- COT in a time- and concentration-dependent manner, both acutely and chronically, through the PDGF receptor. The acute effect occurs at the post-translational level whereas the chronic effect may involve regulation through gene expression. Regulation by PDGF involves the signalling molecules phosphoinositides 3-kinase and protein phosphatase-1. Finally, the NO/cGMP/protein kinase G pathway, involved in vasodilation and hence cardiovascular disease, regulates K+-Cl- COT in VSMCs at the mRNA expression and transport levels. A complex and diverse array of mechanisms and effectors regulate K+-Cl- COT and thus cell volume homeostasis, setting the stage for abnormalities at the genetic and/or regulatory level thus effecting or being affected by various pathological conditions.

Electrokinetic properties of tantalum oxide deposited on model substrate in NaCl and LiCl solutions

International Nuclear Information System (INIS)

Sidorova, M.P.; Bogdanova, N.F.; Ermakova, L.Eh.; Bobrov, P.V.

1997-01-01

Electrokinetic characteristics of tantalum oxide have been studied using a model system - a plane-parallel capillary in chloride solutions containing monocharge (H + , Na + , Li + ) counterions in a wide range of pH and concentrations. It is shown that position of isoelectric point (IEP) of Ta 2 O 5 depends on concentration and type of counterion, moreover, the dependence is not explained in the framework of classical notions of the influence of counterion specific adsorption on IEP position. Electrokinetic potential of Ta 2 O-5 surface at the background of diluted LiCl solutions is higher in its absolute value, than at the background of NaCl solutions according to direct lyotropic series. The results of measurements of the capillary resistance dependence on pH at the background of NaCl and LiCl solutions 10 -3 -10 -1 M are used for the calculation of efficiency and specific surface conductivity factors

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

NARCIS (Netherlands)

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

2009-01-01

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

Regulation of K-Cl cotransport: from function to genes.

Science.gov (United States)

Adragna, N C; Di Fulvio, M; Lauf, P K

2004-10-01

This review intends to summarize the vast literature on K-Cl cotransport (COT) regulation from a functional and genetic viewpoint. Special attention has been given to the signaling pathways involved in the transporter's regulation found in several tissues and cell types, and more specifically, in vascular smooth muscle cells (VSMCs). The number of publications on K-Cl COT has been steadily increasing since its discovery at the beginning of the 1980s, with red blood cells (RBCs) from different species (human, sheep, dog, rabbit, guinea pig, turkey, duck, frog, rat, mouse, fish, and lamprey) being the most studied model. Other tissues/cell types under study are brain, kidney, epithelia, muscle/smooth muscle, tumor cells, heart, liver, insect cells, endothelial cells, bone, platelets, thymocytes and Leishmania donovani. One of the salient properties of K-Cl-COT is its activation by cell swelling and its participation in the recovery of cell volume, a process known as regulatory volume decrease (RVD). Activation by thiol modification with N-ethylmaleimide (NEM) has spawned investigations on the redox dependence of K-Cl COT, and is used as a positive control for the operation of the system in many tissues and cells. The most accepted model of K-Cl COT regulation proposes protein kinases and phosphatases linked in a chain of phosphorylation/dephosphorylation events. More recent studies include regulatory pathways involving the phosphatidyl inositol/protein kinase C (PKC)-mediated pathway for regulation by lithium (Li) in low-K sheep red blood cells (LK SRBCs), and the nitric oxide (NO)/cGMP/protein kinase G (PKG) pathway as well as the platelet-derived growth factor (PDGF)-mediated mechanism in VSMCs. Studies on VSM transfected cells containing the PKG catalytic domain demonstrated the participation of this enzyme in K-Cl COT regulation. Commonly used vasodilators activate K-Cl COT in a dose-dependent manner through the NO/cGMP/PKG pathway. Interaction between the

In-line monitoring of an oxide ion in LiCl molten salt using a YSZ based oxide ion selective electrode

International Nuclear Information System (INIS)

Cho, Young Hwan; Jeon, Jong Seon; Yeon, Jei Won; Choi, In Kyu; Kim, Won Ho

2004-01-01

The electrode potential characteristics of a YSZ based membrane metal oxide electrode have been studied in molten LiCl at 700 .deg. C by the potentiometric method. The electrode exhibited a good potential response to log[O 2 ] and data reproducibility. The calibration plot (potential vs. log[O 2 ] was found to be linear, obeying the nernst equation. The electrode potential showed a good reversibility corresponding to increase/decrease of the oxide ion present in the molten LiCl. The physical and chemical durability appeared to be sound after several repeated uses, resulting in reproducible results. However, 'the proposed electrode' failed when metallic Li was present in the melt

Preparation and Humidity Sensing Properties of KCl/MCM-41 Composite

International Nuclear Information System (INIS)

Li, Liu; Lian-Yuan, Wang; Wei, Li; Li-Ying, Kou; Zhi-Cheng, Zhong; Li-Fang, Liu

2010-01-01

KCl/mobil composition of matter-41 (MCM-41) composite has been synthesized via a heat-treating process and characterized by x-ray diffraction, high resolution transmission electron microscopy, and nitrogen adsorption/desorption isotherms. In contrast with pure MCM-41, KCl/MCM-41 composite exhibits improved humidity sensing properties within the relative humidity range of 11–95%. The impedance of KCl/MCM-41 composite changes by about four orders of magnitude over the whole humidity range with the response time and the recovery times are about 30 s and 35 s, respectively. Small humidity hysteresis and good stability are also observed based on our product. These results make our product a good candidate in fabricating humidity sensors with high performances and low synthetic complexity

Dynamic Network Reconstruction from Gene Expression Data Describing the Effect of LiCl Stimulation on Hepatocytes

Directory of Open Access Journals (Sweden)

Zellmer Sebastian

2005-12-01

Full Text Available Wnt/β-catenin signalling plays an important role in zonation of liver parenchyma and in patterning of hepatocyte heterogeneity. A characteristic marker of this heterogeneity is glutamine synthetase, which is expressed only in a subset of pericentrally located hepatocytes. To investigate, whether and how the Wnt/β-catenin signalling pathway is involved a culture of hepatocytes was stimulated by LiCl. This resulted in an increase in the specific GS activity, indicating that the Wnt/β-catenin pathway may participate in regulating GS levels. Affymetrix GeneChip oligonucleotide arrays were used to monitor the gene expression changes during a period from 2 to 24 hours after stimulation by LiCl. Samples from a cultivation without stimulation were used as controls. Based on the gene expression profiles a hypothetic signal transduction network was constructed by a reverse engineering algorithm. The network robustness was tested and the most stable structure was identified.

Study of an F center in molten KCl

Energy Technology Data Exchange (ETDEWEB)

Parrinello, M.; Rahman, A.

1984-01-15

It is shown that a discretized version of Feynman's path integral provides a convenient tool for the numerical investigation of the properties of an electron solvated in molten KCl. The binding energy, the magnetic susceptibility, and the pair correlation functions are calculated. The local structure around the solute electron appears to be different from that of an F center in the solid. The Feynman path of the electron dissolved in molten KCl is highly localized thus justifying the F center model. The effect of varying the e/sup -/-K/sup +/ pseudopotential is also reported.

The applicability of activities in kinetic expressions: A more fundamental approach to represent the kinetics of the system CO2–OH-salt in terms of activities

NARCIS (Netherlands)

Haubrock, J.; Hogendoorn, Kees; Versteeg, Geert

2007-01-01

The applicability of utilizing activities instead of concentrations in kinetic expressions has been investigated using the reaction of CO2 in sodium hydroxide solutions also containing different neutral salts (LiCl, KCl and NaCl) as model system. For hydroxide systems it is known that when the

Electrochemical Behavior of LiBr, LiI, and Li2Se in LiCl Molten Salt

International Nuclear Information System (INIS)

Choi, In Kyu; Do, Jae Bum; Hong, Sun Seok; Seo, Chung Seok

2006-03-01

The effect of fission products on the electrolytic reduction of uranium oxide has been studied. It has been reported that volatile fission products, such as Br, I, and Se, react with Li metal which is a reductant in the process to give LiBr, LiI, and Li 2 Se. These compounds are dissociated as corresponding anions and cations in the LiCl molten salt at 650 .deg. C. In this experiment, oxidation and reduction reaction of 3wt% of each compound in LiCl molten salt were investigated by cyclic voltammetry. For LiBr, redox reactions of cation and anion were reversible, while redox reactions of Li + and I - were irreversible. For Li 2 Se, about half of the produced Li metal was disappeared at the cathode and two anodic current curves were appeared. After the cyclic voltammetric measurements for each compound, chronopotentiometric experiment was carried out for one hour with 100 - 400 mA. After the electrolysis, no compounds gave Li metal in the porous MgO filter in which Li metal was produced at the cathode. However, LiCl salt was covered with Br 2 for LiBr electrolysis. Dark red color of Br 2 was easily removed by water. For LiI electrolysis, salt gave black color and I 2 was deposited on the Pt anode. For Li 2 Se electrolysis, black fine powders were precipitated in the salt. After the separation and dryness of the precipitates, it was analyzed with XRD and it turned out PtSe 2 . From the electrochemical experimental results, it was concluded that these compounds may affect the electrolytic reduction process of uranium oxide in the spent fuel

Is KCl(g) corrosive at temperatures above its dew point? Influence of KCl(g) on initial stages of the high temperature corrosion of 11% Cr steel at 600 C

Energy Technology Data Exchange (ETDEWEB)

Segerdahl, K.; Pettersson, J.; Svensson, J.E.; Johansson, L.G. [Dept. of Environmental Inorganic Chemistry, High Temperature Corrosion Centre, Chalmers Univ. of Technology, Goeteborg (Sweden)

2004-07-01

The influence of gaseous KCl on the high temperature oxidation of CrMoV11 1 (X20) steel at 600 C is reported. The sample temperature was above the dew point of KCl, the partial pressure of KCl being about 5ppm. The samples were investigated by a number of surface analytical techniques including grazing angle XRD, SEM/EDX, and SAM. CrMoV11 1 steel shows protective behaviour in clean dry O{sub 2} and O{sub 2}/H{sub 2}O environment because of the formation of a chromium-rich oxide ({alpha}-(Fe,Cr){sub 2}O{sub 3}). It is often considered that alkali salts accelerate the corrosion of steel only when present on the surface in solid or liquid form. In contrast, the present result shows that gaseous KCl is very corrosive, also in the absence of condensation. KCl(g) reacts with chromium in the scale, forming K{sub 2}CrO{sub 4}(s). This depletes the protective oxide in chromium and leads to the formation of non-protective hematite, Fe{sub 2}O{sub 3}. (orig.)

Processing of Vietnamese lithium ores to produce LiCl

International Nuclear Information System (INIS)

Dinh, Thi Thu Hien

2015-01-01

A potential lithium deposit has been discovered in the La Vi mining district, located in Quang Ngai Province, Central Vietnam. The Li-rich rocks (average contents: 1.3±0.9 wt.% Li 2 O) are highly fractionated, peraluminous granites, which are further characterized by high contents of Al 2 O 3 , Na 2 O, K 2 O, F, and P 2 O 5 , but very low concentrations of all other main components (MgO, CaO, Fe 2 O 3 tot, TiO 2 ). The granites exhibit a light pink color and contain mainly albite, quartz, muscovite, lithian muscovite, and lepidolite, with minor amounts of amblygonite-montebrasite, herderite, fluorapatite, topaz, and cassiterite, and accessory beryl and goyazite. Lepidolite from La Vi deposit was extracted to produce lithium chloride by using iron II sulphide (FeS)-CaO roasting and water leaching. The HSC program was applied for the simulation of the behavior of lepidolite and the additives during roasting, confirming the important role of SO 2 /SO 3 gas for extracting lithium from lepidolite. At optimum conditions roasting at 750 C using FeS/Li and Ca/F molar ratios of 5:1 and 1:1, respectively, followed by leaching at 50 C using water/calcine mass ratios of >5:1 could yield a maximum of ∝85% Li recovery (at <1 g/L Li concentration). Addition of CaO led to a decrease in the liberation of HF gas and insoluble LiF formation. NaOH and BaCl 2 were used for removing the metal and sulphate impurities from the leach liquor by precipitation at ambient temperature. The efficiency of lithium extraction reached ∝100 % with washing of the precipitates after filtering. Alkali salts were separated from the LiCl solution via solar evaporation and isopropanol leaching. 96.3 wt.% LiCl could be produced using an isopropanol/salt mass ratio of 5:1 at ambient temperature in 3 h.

Processing of Vietnamese lithium ores to produce LiCl

Energy Technology Data Exchange (ETDEWEB)

Dinh, Thi Thu Hien

2015-11-16

A potential lithium deposit has been discovered in the La Vi mining district, located in Quang Ngai Province, Central Vietnam. The Li-rich rocks (average contents: 1.3±0.9 wt.% Li{sub 2}O) are highly fractionated, peraluminous granites, which are further characterized by high contents of Al{sub 2}O{sub 3}, Na{sub 2}O, K{sub 2}O, F, and P{sub 2}O{sub 5}, but very low concentrations of all other main components (MgO, CaO, Fe{sub 2}O{sub 3}tot, TiO{sub 2}). The granites exhibit a light pink color and contain mainly albite, quartz, muscovite, lithian muscovite, and lepidolite, with minor amounts of amblygonite-montebrasite, herderite, fluorapatite, topaz, and cassiterite, and accessory beryl and goyazite. Lepidolite from La Vi deposit was extracted to produce lithium chloride by using iron II sulphide (FeS)-CaO roasting and water leaching. The HSC program was applied for the simulation of the behavior of lepidolite and the additives during roasting, confirming the important role of SO{sub 2}/SO{sub 3} gas for extracting lithium from lepidolite. At optimum conditions roasting at 750 C using FeS/Li and Ca/F molar ratios of 5:1 and 1:1, respectively, followed by leaching at 50 C using water/calcine mass ratios of >5:1 could yield a maximum of ∝85% Li recovery (at <1 g/L Li concentration). Addition of CaO led to a decrease in the liberation of HF gas and insoluble LiF formation. NaOH and BaCl{sub 2} were used for removing the metal and sulphate impurities from the leach liquor by precipitation at ambient temperature. The efficiency of lithium extraction reached ∝100 % with washing of the precipitates after filtering. Alkali salts were separated from the LiCl solution via solar evaporation and isopropanol leaching. 96.3 wt.% LiCl could be produced using an isopropanol/salt mass ratio of 5:1 at ambient temperature in 3 h.

Obtainment of lithium metal by electrolysis of molten salts

International Nuclear Information System (INIS)

Silva Costa, M.A.Z. da.

1988-04-01

The obtainment metallic lithium through KCL + LiCl, using a stainless steel cathode and a graphite anode is studied. The applications of lithium on nuclear energy, aerospatial program, metalurgy and as refining and degassing agent are also presented. The purification of lithium is still mentioned. (C.G.C.) [pt

Ionic conductivity in irradiated KCL; Conductiviad ionica de KCL irradiado

Energy Technology Data Exchange (ETDEWEB)

Vignolo Rubio, J

1979-07-01

The ionic conductivity of X and gamma irradiated KCL single crystals has been studied between room temperature and 600 degree centigree. the radiation induced damage resulting in a decrease of the conductivity heals by thermal annealing in two steps which are at about 350 and 550 degree centigree respectively. It has been found that the radiation induced colour centres are not involved in the observed decrease of the ionic conductivity. However. It has been observed that the effects of quenching and plastic deformation on the conductivity of the samples are very similar to the effect induced by irradiation. It is suggested that, samples radiation induced dislocation loops might cause the ionic conductivity decrease observed in irradiated samples. (Author)

The phase diagram of KNO3-KClO3

International Nuclear Information System (INIS)

Zhang Xuejun; Tian Jun; Xu Kangcheng; Gao Yici

2004-01-01

The binary phase diagram of KNO 3 -KClO 3 is studied by means of differential scanning calorimetry (DSC) and high-temperature X-ray diffraction. The limited solid solutions, K(NO 3 ) 1-x (ClO 3 ) x (0 3 ) 1-x (ClO 3 ) x (0.90 3 -based solid solutions and KClO 3 -based solid solutions phase, respectively. For KNO 3 -based solid solutions, KNO 3 ferroelectric phase can be stable from 423 to 223 K as a result of substituting of NO 3 by ClO 3 -radicals. The temperatures for solidus and liquidus have been determined based on limited solid solutions. Two models, Henrian solution and regular solution theory for KNO 3 -based (α) phase and KClO 3 -based (β) phase, respectively, are employed to reproduce solidus and liquidus of the phase diagram. The results are in good agreement with the DSC data. The thermodynamic properties for α and β solid solutions have been derived from an optimization procedure using the experimental data. The calculated phase diagram and optimized thermodynamic parameters are thermodynamically self-consistent

Reduction behaviors of Zr for LiCl-KCl-ZrCl4 and LiCl-KCl-ZrCl4-CdCl2

International Nuclear Information System (INIS)

Kim, Si Hyung; Yoon, Jongho; Kim, Gha Young; Kim, Tack Jin; Shim, Joon Bo; Kim, Kwang Rag; Jung, Jae Hoo; Ahn, Do Hee; Paek, Seungwoo

2013-01-01

The reduction potentials of most of the zirconium ions on the solid cathode are smaller (about 0.4V) than that of uranium, and thus zirconium can be recovered prior to uranium during the reduction stage. In the case of a liquid cadmium cathode, which is one of the major cathodes, the reduction potential can be changed because zirconium reacts with the liquid cadmium. Up to now, it has not been well known what the reduction potential of Zr was on the liquid Cd cathode. According to the Cd-Zr phase diagram, there are four intermetallic compounds between cadmium and zirconium. It is easier to use the solid cathode than the liquid cadmium cathode in LiCl-KCl-ZrCl 4 containing CdCl 2 to identify the formation of the Cd-Zr phase. In this study, the reduction behaviors of zirconium were compared in the LiCl-KCl-ZrCl 4 and LiCl-KCl-ZrCl 4 -CdCl 2 solutions when using a solid cathode. The reduction behavior of Zr at a solid W cathode and a Cd-coated W cathode was compared in a LiCl-KCl-ZrCl 4 solution at 500 .deg. C. It was observed from the results using a solid W cathode that Zr 4+ ions were gradually oxidized to Zr 2+ , Zr, and ZrCl during the reduction sweep, but the final oxidation peak of Zr 2+ to Zr 4+ seemed to be unclear during the oxidation sweep. In the case of the Cd-coated W electrode, only a Cd 2 Zr phase was formed at 500 .deg. C, which seemed to be related to the melting point of Cd-Zr intermetallics. Through additional studies at different temperatures, the formation behavior will be studied

The Effect of LiCl and Coagulation Bath Temperature on the Structure and Performance of PVDF Membranes

Directory of Open Access Journals (Sweden)

Marzieh Sedaghat

2015-09-01

Full Text Available Polyvinylidene fluoride (PVDF membranes are widely used in microfiltration and ultrafiltration processes for their excellent mechanical and chemical resistance and thermal stability in comparison with other polymeric membranes. Non-solvent induced phase separation (NIPS is the most important method by which the PVDF membranes are prepared. The structure of the membranes prepared by NIPS method depends on different parameters including the concentration of the polymer solution, polymer molecular weight, the composition and temperature of coagulation bath, type of solvent and the presence of additives in the initial solution. In the present work, the effects of coagulation bath temperature and LiCl content of the dope solution were studied with respect to the structure and performance of PVDF membranes. N-Methyl-2-pyrrolidone and water were used as solvent and coagulation bath, respectively. A set of analytical techniques including: scanning electron microscopy, mechanical test, pure water permeability and mean pore radius of pores was used to characterize the membranes. Moreover, the separation of humic acid, a main biological contaminant in surface water resources, was studied to determine membranes performance. The results show that at constant coagulation bath temperature, presence of LiCl in the dope solution increased the number as well as the mean pore radius of the pores at the surface of membranes and consequently, pure water permeability of the membranes was increased, whereas, the mechanical strength and humic acid rejection of the membranes were dropped. Moreover, at a constant content of LiCl, increasing the coagulation bath temperature decreased the size of macrovoids so that the mechanical strength as well as humic acid rejection of the membranes was increased.

Purification of used eutectic (LiCl-KCl) salt electrolyte from pyroprocessing

Science.gov (United States)

Cho, Yung-Zun; Lee, Tae-Kyo; Eun, Hee-Chul; Choi, Jung-Hoon; Kim, In-Tae; Park, Geun-Il

2013-06-01

The separation characteristics of surrogate rare-earth fission products in a eutectic (LiCl-KCl) molten salt were investigated. This system is based on the eutectic salt used for the pyroprocessing treatment of used nuclear fuel (UNF). The investigation was performed using an integrated rare-earth separation apparatus comprising a precipitation reactor, a solid detachment device, and a layer separation device. To separate rare-earth fission products, a phosphate precipitation method using both Li3PO4 and K3PO4 as a precipitant was performed. The use of an equivalent phosphate precipitant composed of 0.408 molar ratio-K3PO4 and 0.592 molar ratio-Li3PO4 can preserve the original eutectic ratio, LiCl-0.592 molar ratio (or 45.2 wt%), as well as provide a high separation efficiency of over 99.5% under conditions of 550 °C and Ar sparging when using La, Nd, Ce, and Pr chlorides. The mixture of La, Nd, Ce, and Pr phosphate had a typical monoclinic (or monazite) structure, which has been proposed as a reliable host matrix for the permanent disposal of a high-level waste form. To maximize the reusability of purified eutectic waste salt after rare-earth separation, the successive rare-earth separation process, which uses both phosphate precipitation and an oxygen sparging method, were introduced and tested with eight rare-earth (Y, La, Ce, Pr, Nd, Sm, Eu and Gd) chlorides. In the successive rare-earth separation process, the phosphate reaction was terminated within 1 h at 550 °C, and a 4-8 h oxygen sparging time were required to obtain over a 99% separation efficiency at 700-750 °C. The mixture of rare-earth precipitates separated by the successive rare-earth separation process was found to be phosphate, oxychloride, and oxide. Through the successive rare-earth separation process, the eutectic ratio of purified salt maintained its original value, and impurity content including the residual precipitant of purified salt can be minimized.

Microneedle crystals of cyano-substituted thiophene/phenylene co-oligomer epitaxially grown on KCl surface

Science.gov (United States)

Torii, Kazuki; Dokiya, Shohei; Tanaka, Yosuke; Yoshinaga, Shohei; Yanagi, Hisao

2017-06-01

A cyno-substituted thiophene/phenylene co-oligomer (TPCO), 5,5‧-bis(4‧-cyanobiphenyl-4-yl)-2,2‧-bithiophene (BP2T-CN), is vapor-deposited on KCl (001) surface kept at 220 °C by the mask-shadowing method. Transmission electron microscopy and fluorescence microscopy reveal that the deposited BP2T-CN crystallizes in two types of morphologies: microneedles and thin film crystallites. In particular, the predominant microneedles epitaxially grow in four directions in the manner that the BP2T-CN molecules align along the [110]KCl or [-110]KCl. X-ray diffraction patterns indicate that the BP2T-CN molecules in the microneedle lie parallel while those in the thin film crystallite obliquely stand on the KCl surface.

Supercrystallization of KCl from solution irradiated by soft X-rays

Science.gov (United States)

Janavičius, A. J.; Rinkūnas, R.; Purlys, R.

2016-10-01

The X-rays influence on KCl crystallization in a saturated water solution has been investigated for the aim of comparing it with previously considered NaCl crystallization. The rate of crystallization has been measured in the drying drop in the solution activated by the irradiation. We have measured the influence of the irradiation time of the solution on the rates of KCl crystallization as well as the beginning of the crystallization processes on drying drops. For a longer irradiation time of the solution early crystallization in the drops occurs. A saturated water solution of KCl was irradiated with the diffractometer DRON-3M (Russian device) and this had a great influence on the two-step processes of crystallization. The ionization of the solution by soft X-rays can produce ions, metastable radicals in water, excited crystals' seeds and vacancies in growing crystals by Auger's effect. The X-rays generate a very fast crystallization in the drying drop.

Circular magnetic dichroism of the Fa center adsorption in KCl doped with Li and Na

International Nuclear Information System (INIS)

Baldacchini, G.; Botti, S.; Grassano, U.M.

1990-01-01

The spin-orbit structure of F A in KCl:Li and KCl:Na have been studied by means of the magnetic circular dichroism. Due to their C 4V , symmetry the F A centers have two different spin-orbit parameters, Δ * and Δ * , which only in the KCl:Li case follow the relation: Δ * F A centers have been determined using the method of moment

First principles study of structural, electronic and optical properties of KCl crystal

International Nuclear Information System (INIS)

Chen, Z.J.; Xiao, H.Y.; Zu, X.T.

2006-01-01

The structural, electronic and optical properties of KCl crystal in B1, B2, B3 and T1 structures have been systematically studied using first-principle pseudopotential calculations. In addition, pressure-induced phase transition has also been investigated. It was found that when the pressure is below 2.8 GPa, the B1 structure is the most stable. Above 2.8 GPa KCl crystal will undergo a structural phase transition from the relatively open NaCl structure into the more dense CsCl atomic arrangement. Our results also suggested that at about 1.2 GPa structural phase transition from B3 to T1 will occur. When the pressure arrives at 39.9 GPa, the phase transition will occur from B2 to T1. In addition, we found KCl Crystal has indirect band gap in B2 structure and direct band gap in B1, B3 and T1 structures. The band gap value is the smallest in the T1 structure and is the largest in the B1 and B3 structures. Our calculations are found to be in good agreement with available experimental and theoretical results. The dielectric function and energy loss function of KCl crystal in four structures (B1, B2, B3 and T1) have been calculated as well as the anisotropy of the optical properties of KCl crystal in T1 structure

Emission of thermally stimulated luminescence in mixed monocrystals KCl-KBr: Pb2+, KCl: Pb2+ and KBr: Pb2+ exposed at low doses

International Nuclear Information System (INIS)

Cruz Z, E.; Ramos B, S.; Melendrez A, R.; Chernov, V.; Piters, T.M.; Barboza F, M.; Hernandez A, J.; Murrieta S, H.

2002-01-01

It is reported the behavior of solid solutions of mixed crystals KCl 1-x KBr x doped with divalent lead which were exposed to gamma radiation. The mixtures of KCl-KBr were varied, with x equivalents at 2, 50, 65, and 85 % including the extremes KCl: Pb 2+ and KBr: Pb 2+ . It was maintained a concentration of divalent lead between 20 and 40 ppm in the crystalline lattice. The production of the generated defects by radiation have been correlated with the increase in the brilliance curves depending on the received dose by the mixed doped crystal. It has been used the thermal stimulation (Tl) for obtaining the crystal luminescence depending on the dose until 130 Gy with gammas of cobalt 60. The results shows that this mixed crystalline material of varied composition responds adequately to low doses which indicates that this would be a good detector of ionizing radiation. The results have been correlated with the optical properties of this mixed doped crystal, however it has been found that exists an important loss of luminescence depending on the halogen quantity presents in the mixed crystal. (Author)

Study of effect of quenching and deformation on KCl: Gd crystals by ...

Indian Academy of Sciences (India)

Unknown

Abstract. The study of ionic conductivity vs reciprocal temperature of pure KCl and KCl crystal doped with. 0⋅1, 0⋅3 and 0⋅5 mole% gadolinium has been carried out in as grown, quenched from elevated temperatures. (100, 350 and 500°C) and annealed at various timings i.e. 2–3 h and deformed by different percentages.

Liquid phase assisted grain growth in Cu2ZnSnS4 nanoparticle thin films by alkali element incorporation

DEFF Research Database (Denmark)

Engberg, Sara Lena Josefin; Canulescu, Stela; Schou, Jørgen

2018-01-01

The effect of adding LiCl, NaCl, and KCl to Cu2ZnSnS4 (CZTS) nanoparticle thin-film samples annealed in a nitrogen and sulfur atmosphere is reported. We demonstrate that the organic ligand-free nanoparticles previously developed can be used to produce an absorber layer of high quality. The films...

K-Cl cotransport function and its potential contribution to cardiovascular disease.

Science.gov (United States)

Adragna, Norma C; Lauf, Peter K

2007-12-01

K-Cl cotransport is the coupled electroneutral movement of K and Cl ions carried out by at least four protein isoforms, KCC1-4. These transporters belong to the SLC12A family of coupled cotransporters and, due to their multiple functions, play an important role in the maintenance of cellular homeostasis. Significant information exists on the overall function of these transporters, but less is known about the role of the specific isoforms. Most functional studies were done on K-Cl cotransport fluxes without knowing the molecular details, and only recently attention has been paid to the isoforms and their individual contribution to the fluxes. This review summarizes briefly and updates the information on the overall functions of this transporter, and offers some ideas on its potential contribution to the pathophysiological basis of cardiovascular disease. By virtue of its properties and the cellular ionic distribution, K-Cl cotransport participates in volume regulation of the nucleated and some enucleated cells studied thus far. One of the hallmarks in cardiovascular disease is the inability of the organism to maintain water and electrolyte balance in effectors and/or target tissues. Oxidative stress is another compounding factor in cardiovascular disease and of great significance in our modern life styles. Several functions of the transporter are modulated by oxidative stress, which in turn may cause the transporter to operate in either "overdrive" with the purpose to counteract homeostatic changes, or not to respond at all, again setting the stage for pathological changes leading to cardiovascular disease. Intracellular Mg, a second messenger, acts as an inhibitor of K-Cl cotransport and plays a crucial role in regulating the activity of protein kinases and phosphatases, which, in turn, regulate a myriad of cellular functions. Although the role of Mg in cardiovascular disease has been dealt with for several decades, this chapter is evolving nowadays at a faster

Phase relations in the system NaCl-KCl-H2O: IV. Differential thermal analysis of the sylvite liquidus in the KCl-H2O binary, the liquidus in the NaCl-KCl-H2O ternary, and the solidus in the NaCl-KCl binary to 2 kb pressure, and a summary of experimental data for thermodynamic-PTX analysis of solid-liquid equilibria at elevated P-T conditions

Science.gov (United States)

Chou, I.-Ming; Sterner, S.M.; Pitzer, Kenneth S.

1992-01-01

The sylvite liquidus in the binary system KCl-H2O and the liquidus in the ternary system NaCl-KCl-H2O were determined by using isobaric differential thermal analysis (DTA) cooling scans at pressures up to 2 kbars. Sylvite solubilities along the three-phase curve in the binary system KCl-H2O were obtained by the intersection of sylvite-liquidus isopleths with the three-phase curve in a P-T plot. These solubility data can be represented by the equation Wt.% KCl (??0.2) = 12.19 + 0.1557T - 5.4071 ?? 10-5 T2, where 400 ??? T ??? 770??C. These data are consistent with previous experimental observations. The solidus in the binary system NaCl-KCl was determined by using isobaric DTA heating scans at pressures up to 2 kbars. Using these liquidus and solidus data and other published information, a thermodynamic-PTX analysis of solid-liquid equilibria at high pressures and temperatures for the ternary system has been performed and is presented in an accompanying paper (Part V of this series). However, all experimental liquidus, solidus, and solvus data used in this analysis are summarized in this report (Part IV) and they are compared with the calculated values based on the analysis. ?? 1992.

Salt-Zeolite Ion Exchange Equilibrium Studies for Complete Set of Fission Products in Molten LiCl-KCl

International Nuclear Information System (INIS)

Yoo, Tae-Sic; Frank, Steven M.; Simpson, Michael F.; Hahn, Paula A.; Battisti, Terry J.; Phongikaroon, Supathorn

2010-01-01

This paper presents results on LiCl-KCl based molten salts/zeolite-A contact experiments and the associated equilibrium ion exchange model. Experiments examine the contact behaviors of various ternary salts (LiCl-KCl-YCl3, LiCl-KCl-LaCl3, and LiCl-KCl-PrCl3) and quaternary salts (LiCl-KCl-CsCl-NdCl3 and LiCl-KCl-CsCl-SrCl2) with the zeolite-A. The developed equilibrium model assumes that there are ion exchange and occlusion sites, both of which are in equilibrium with the molten salt phase. A systematic approach in estimating total occlusion capacity of the zeolite-A is developed. The parameters of the model, including the total occlusion capacity of the zeolite-A, were determined from fitting experimental data collected via multiple independent studies including the ones reported in this paper. Experiments involving ternary salts were used for estimating the parameters of the model, while those involving quaternary salts were used to validate the model.

Effect of NaCl and KCl on irradiated diploid yeast cells

International Nuclear Information System (INIS)

Amirtaev, K.G.; Lobachevskij, P.N.; Lyu Gvan Son

1984-01-01

Irradiated dipload yeast Saccharomyces cerevisiae kept in NaCl and KCl solutions died more readily than nonirradiated cells: the death rate was a functaon of radiation Jose and temperature of exposure. It was suggested that the radiation-induced injury to mass cell structures was responsible for the death rate. It was shown that the postirradiataon recovery of cells from radiation damages proceeded in KCl solution two-three times slower than mn water, and it was inhibited completely in NaCl solution

Phase relations in the hydrous CMAS pyrolite in presence of KCl at 2 GPa

Science.gov (United States)

Safonov, O.

2012-04-01

In the upper mantle, chlorides are constituents of concentrated aqueous solutions (brines), as well as chloride-carbonate and carbonatite melts. Mineral assemblages coming from diverse depth levels show that mobile (K, Na)Cl-bearing fluids are able to provoke intensive metasomatism of the peridotitic mantle accompanied by melting. Scarce experimental studies on influence of brines on mineral equilibria in the peridotitic mantle (Stalder et al., 2008; Chu et al., 2011) indicate that influence of chlorides on water activity in a fluid equilibrated with forsterite enstatite at pressures above 2 GPa is very similar to their effect at lower "crustal" pressures (e.g. Aranovich, Newton, 1997): decrease of the H2O activity with an increase of the salt content results in an increase of the melting temperature of silicates. Nevertheless, these experiments were performed in the Al-free systems. Presence of Al would provoke an active interaction of alkali chlorides, namely KCl, with silicates with formation of new K-Al-bearing phases, such as phlogopite (in presence of H2O), which would influence on the melting of complex assemblages. In order to investigate an effect of KCl on phase relations in the Al2O3, CaO, Na2O-rich hydrous peridotite and on stability of garnet, pyroxenes, and amphiboles, in particular, experiments on interaction of the model CMAS pyrolite Fo57En17Prp14Di12 (+0.3 wt. % of Na2O) with the H2O-KCl fluid were performed at 2 GPa in the temperature interval 900-1200. Mixtures of synthetic forsterite, diopside, enstatite and pyrope in the above weight ratio were mixed with 14 wt. % of Mg(OH)2 corresponding to 4.4 wt. % of H2O in the system. 2.4, 3.7, 5 and 10 wt. % of KCl were added to silicate-H2O mixture. Experiments were performed using a piston-cylinder apparatus with ½-inch talc high-pressure cells calibrated via brucite = periclase + H2O and albite = jadeite + quartz equilibria curves. Temperature was controlled with accuracy ?1 with the W95Re5/W80Re20

High-Order Ca(II)-Chloro Complexes in Mixed CaCl2-LiCl Aqueous Solution: Insights from Density Functional Theory and Molecular Dynamics Simulations.

Science.gov (United States)

Wang, Yu-Lin; Wang, Ying; Yi, Hai-Bo

2016-07-21

In this study, the structural characteristics of high-coordinated Ca-Cl complexes present in mixed CaCl2-LiCl aqueous solution were investigated using density functional theory (DFT) and molecular dynamics (MD) simulations. The DFT results show that [CaClx](2-x) (x = 4-6) clusters are quite unstable in the gas phase, but these clusters become metastable when hydration is considered. The MD simulations show that high-coordinated Ca-chloro complexes are possible transient species that exist for up to nanoseconds in concentrated (11.10 mol·kg(-1)) Cl(-) solution at 273 and 298 K. As the temperature increases to 423 K, these high-coordinated structures tend to disassociate and convert into smaller clusters and single free ions. The presence of high-order Ca-Cl species in concentrated LiCl solution can be attributed to their enhanced hydration shell and the inadequate hydration of ions. The probability of the [CaClx](2-x)aq (x = 4-6) species being present in concentrated LiCl solution decreases greatly with increasing temperature, which also indicates that the formation of the high-coordinated Ca-Cl structure is related to its hydration characteristics.

Activity coefficients of LiCl in (PEG 4000 + water) at T = (288.15, 298.15, and 308.15) K

International Nuclear Information System (INIS)

Morales, Jaime W.; Galleguillos, Hector R.; Graber, Teofilo A.; Hernandez-Luis, Felipe

2010-01-01

The electromotive force of the cell containing two ion-selective electrodes (ISE), Na-ISE|LiCl(m),PEG4000(w),H 2 O(1-w)|Cl-ISE has been measured at temperatures of (288.15, 298.15, and 308.15) K as a function of the mass fraction of PEG 4000 (w) in the mixture. w was varied between 0 and 0.25 in 0.05-unit steps and the molality of the electrolyte (m) was between c.a. (0.03 and 5.8) mol . kg -1 . The values of the standard electromotive force, E 0 , were determined using routine methods of extrapolation, together with extended Debye-Hueckel and Pitzer equations. The results obtained produced good internal consistency for all the temperatures studied. Once E 0 was determined, the mean ionic activity coefficients for LiCl, the Gibbs free energy of transfer from the water to (PEG 4000 + water), and the primary LiCl hydration number were calculated.

Activity coefficients of LiCl in (PEG 4000 + water) at T = (288.15, 298.15, and 308.15) K

Energy Technology Data Exchange (ETDEWEB)

Morales, Jaime W.; Galleguillos, Hector R.; Graber, Teofilo A. [Centro de Investigacion Cientifico y Tecnologico para la Mineria, Departamento de Ingenieria Quimica, Universidad de Antofagasta (Chile); Hernandez-Luis, Felipe, E-mail: ffhelu@ull.e [Departamento de Quimica Fisica, Universidad de La Laguna, Tenerife (Spain)

2010-10-15

The electromotive force of the cell containing two ion-selective electrodes (ISE), Na-ISE|LiCl(m),PEG4000(w),H{sub 2}O(1-w)|Cl-ISE has been measured at temperatures of (288.15, 298.15, and 308.15) K as a function of the mass fraction of PEG 4000 (w) in the mixture. w was varied between 0 and 0.25 in 0.05-unit steps and the molality of the electrolyte (m) was between c.a. (0.03 and 5.8) mol . kg{sup -1}. The values of the standard electromotive force, E{sup 0}, were determined using routine methods of extrapolation, together with extended Debye-Hueckel and Pitzer equations. The results obtained produced good internal consistency for all the temperatures studied. Once E{sup 0} was determined, the mean ionic activity coefficients for LiCl, the Gibbs free energy of transfer from the water to (PEG 4000 + water), and the primary LiCl hydration number were calculated.

Viscosity of melts of the system KCl-KBF4-K2TiF6

International Nuclear Information System (INIS)

Nguyen, D.K.; Danek, V.

1997-01-01

The viscosity of melts of the system KCl-KBF 4 -K 2 TiF 6 has been measured by means of the computerized torsional pendulum method. The viscosity of KCl is higher that of KBF 4 at the same temperature, most probably due to the substantial overheating of KBF 4 . In the ternary system the viscosity increases with increasing with increasing content of K 2 TiF 6 . Additivity of algorithms of viscosity was adopted as the ideal behaviour of the mixture. Negative deviations from such additive behaviour were found in the binary system KCl-KBF 4 probably due to the breaks of the weak B-Cl-B bridges caused by the excess of Cl - ions. Positive deviations from the ideal behaviour were found in the binaries KCl-K 2 TiF 6 and KBF 4 -K 2 TiF 6 due to the formation of larger anions TiF 6 Cl 3- and TiF 7 3- caused by the reactions K 2 TiF 6 (l) + KCl(l) = K 3 TiF 6 Cl(l) and KBF 4 (l) + K 2 TiF 6 (l) = K 3 TiF 7 (l) + BF 3 (g). Statistically significant ternary interaction confirmed that the above chemical reactions take place also in the ternary system. (authors)

Electric conductivity of salt melts containing KCL, KF and K2TaF7

International Nuclear Information System (INIS)

Agulyanskij, A.I.; Stangrit, P.T.; Konstantinov, V.I.

1978-01-01

Given are electric conductivity measurement results depending on the temperature and composition of the molten KF-K 2 TaF 7 , KCl-K 2 TaF 7 systems and also melts close in their composition to industrial electrolytes, KCl-KF (in mass ratio of 2:1) with addition of K 2 TaF 7 up to 25 mass%. Presented are electric conductivity molecular isotherms of the KF-K 2 TaF 7 , KCl-K 2 TaF 7 systems at 800 deg C and specific electric conductivity dependence of KCl-KF-K 2 TaF 7 melts on K 2 TaF 7 composition at 800 deg C and 900 deg C. Proceeding from the shape of molecular and specific electric conductivity isotherms a conclusion is made about existence of the following tantalum-containing ions: TaF 7 2- , TaF 6 - and TaF 6 Cl 2- in the investigated melts

Strategies to reduce gaseous KCl and chlorine in deposits during combustion of biomass in fluidised bed boilers

Energy Technology Data Exchange (ETDEWEB)

Kassman, Haakan

2012-11-01

Combustion of a biomass with an enhanced content of alkali and chlorine (Cl) can result in operational problems including deposit formation and superheater corrosion. The strategies applied to reduce such problems include co-combustion and the use of additives. In this work, measures were investigated in order to decrease the risk of superheater corrosion by reducing gaseous KCl and the content of chlorine in deposits. The strategies applied were sulphation of KCl by sulphur/sulphate containing additives (i.e. elemental sulphur (S) and ammonium sulphate (AS)) and co-combustion with peat. Both sulphation of KCl and capture of potassium (K) in ash components can be of importance when peat is used. The experiments were mainly performed in a 12 MW circulation fluidised bed (CFB) boiler equipped for research purposes but also in a full-scale CFB boiler. The results were evaluated by means of IACM (on-line measurements of gaseous KCl), conventional gas analysis, deposit and corrosion probe measurements and ash analysis. Ammonium sulphate performed significantly better than elemental sulphur. Thus the presence of SO{sub 3} (i.e. AS) is of greater importance than that of SO{sub 2} (i.e. S) for sulphation of gaseous KCl and reduction of chlorine in deposits. Only a minor reduction of gaseous KCl was obtained during co-combustion with peat although chlorine in the deposits was greatly reduced. This reduction was supposedly due to capture of K by reactive components from the peat ash in parallel to sulphation of KCl. These compounds remained unidentified. The effect of volatile combustibles on the sulphation of gaseous KCl was investigated. The poorest sulphation was attained during injection of ammonium sulphate in the upper part of the combustion chamber during the lowest air excess ratio. The explanation for this is that SO{sub 3} was partly consumed by side reactions due to the presence of combustibles. These experimental results were supported by modelling, although the

Characteristics of YBa2Cu3O7 high-Tc superconductor with KCl

Science.gov (United States)

Yoon, Ki Hyun; Chang, Sung Sik

1990-03-01

The lattice parameters, microstructural change, transition temperature, and electrical properties of the YBa2-xKxCu3O7 high-Tc superconductor in the range from x=0 to x=0.25 have been investigated. The high-Tc orthorhombic phase increases with increasing KCl up to x=0.20, above which it decreases. The lattice parameters decrease with increasing KCl up to x=0.10, and then become nearly uniform. The grain size increases with increasing KCl up to x=0.20 due to its role as sintering agent. The specimens with x=0.2 have transition temperatures of 96 K and high magnetic susceptibility due to the contraction of lattice parameters a and b and the increase of orthorhombic distortion.

Supercooling of aqueous NaCl and KCl solutions under acoustic levitation.

Science.gov (United States)

Lü, Y J; Wei, B

2006-10-14

The supercooling capability of aqueous NaCl and KCl solutions is investigated at containerless state by using acoustic levitation method. The supercooling of water is obviously enhanced by the alkali metal ions and increases linearly with the augmentation of concentrations. Furthermore, the supercooling depends on the nature of ions and is 2-3 K larger for NaCl solution than that for KCl solution in the present concentration range: Molecular dynamics simulations are performed to reveal the intrinsic correlation between supercoolability and microstructure. The translational and orientational order parameters are applied to quantitatively demonstrate the effect of ionic concentration on the hydrogen-bond network and ice melting point. The disrupted hydrogen-bond structure determines essentially the concentration dependence of supercooling. On the other hand, the introduced acoustic pressure suppresses the increase of supercooling by promoting the growth and coalescence of microbubbles, the effective nucleation catalysts, in water. However, the dissolved ions can weaken this effect, and moreover the degree varies with the ion type. This results in the different supercoolability for NaCl and KCl solutions under the acoustic levitation conditions.

X-ray diffraction measurements in KCl shocked along [100

International Nuclear Information System (INIS)

D'Almeida, T.; Gupta, Y.M.

2000-01-01

Real time x-ray diffraction measurements were used to examine the polymorphic phase transformation in KCl shocked along the [100] direction. Shock wave continuum data, obtained previously by Hayes, were used to design the experiments and to predict diffraction from KCl shocked to different peak stresses. Here, we present the results obtained below the transition stress: between 1.4 and 2 GPa. Diffraction data obtained were quantitatively related to macroscopic compression. Interplanar spacing measurements revealed isotropic compression of the unit cell in contrast to previously reported results. Above the transition stress, descriptions of the atomic arrangement with respect to shock propagation (not available in the literature) are required for setting up the detection system. Hence, continuum results in combination with various crystallographic considerations were utilized to obtain data above the transition stress

Microstructural study of codeposited pentacene:perfluoropentacene grown on KCl by TEM techniques

Science.gov (United States)

Félix, Rocío; Breuer, Tobias; Witte, Gregor; Volz, Kerstin; Gries, Katharina I.

2017-08-01

Transmission electron microscopy techniques have been used as a research tool to derive information on structure and orientation of organic semiconductor blends. Within this work, we have studied the structure and morphology of pentacene (PEN, C22H14) and perfluoropentacene (PFP, C22F14) blends grown with [2:1] and [1:2] mixing ratios on KCl substrates. The [2:1] mixture exhibits a uniform layer on the substrate with domains that are rotated in-plane by 90° towards each other. Electron diffraction experiments revealed that these domains are formed by a crystalline mixed phase (consisting of PEN and PFP) and a PEN phase in excess whose lattice parameters are rather similar. By contrast, in the [1:2] blend, two different arrangements were found. The majority of the sample exhibits some spicular fibers on a background layer lying on top of the KCl substrate. The microstructural characterization revealed that these fibers consist of pure PFP in excess while the background layer is formed by the mixed phase. The other arrangement, which is present to a lesser extent, consists of a PFP film that is in direct contact with the KCl substrate. Using electron diffraction experiments, the orientation of the different phases with respect to each other and in some cases relative to the KCl substrate has been determined.

Modeling of aqueous electrolyte solutions with perturbed-chain statistical associated fluid theory

DEFF Research Database (Denmark)

Cameretti, Luca F.; Sadowski, Gabriele; Mollerup, Jørgen

2005-01-01

The vapor pressures and liquid densities of single-salt electrolyte solutions containing NaCl, LiCl, KCl, NaBr, LiBr, KBr, NaI, LiI, KI, Li2SO4, Na2SO4, and K2SO4 were modeled with an equation of state based on perturbed-chain statistical associated fluid theory (PC-SAFT). The PC-SAFT model...

FUSED SALT METHOD FOR COATING URANIUM WITH A METAL

Science.gov (United States)

Eubank, L.D.

1959-02-01

A method is presented for coating uranium with a less active metal such as Cr, Ni, or Cu comprising immersing the U in a substantially anhydrous molten solution of a halide of these less active metals in a ternary chloride composition which consists of selected percentages of KCl, NaCl and another chloride such as LiCl or CaCl/sub 2/.

Evaluation study of an ion selective field effect transistor electrode for measuring quality parameters of fuel ethanol

Energy Technology Data Exchange (ETDEWEB)

Gonzaga, Fabiano B.; Sobral, Sidney P.; Ribeiro, Carla M.; Goncalves, Mary A., E-mail: fbgonzaga@inmetro.gov.br [Instituto Nacional de Metrologia, Qualidade e Tecnologia(INMETRO), Duque de Caxias, RJ (Brazil). Div. de Metrologia Quimica

2013-01-15

An ion selective field effect transistor (ISFET) electrode was evaluated for measuring pH and acid number (AN) of fuel ethanol and compared to two glass electrodes with different reference filling solutions: KCl aqueous solution (glass-KCl electrode)and LiCl ethanolic solution (glass-LiCl electrode). pH was determined at different measurement times and AN was determined using automatic potentiometric titration. For pH, the glass-KCl electrode showed the best precision and stability, with an average repeatability about four times better when compared to the ISFET electrode for the measurement time of 30 s (as indicated in the ASTM D6423 standard). For AN, the glass-KCl and glass-LiCl electrodes showed similar repeatabilities, which were about three times better than that of the ISFET electrode. In addition, the results from a recovery study demonstrated better accuracy of the glass-LiCl electrode, with a recovery value of 100.1% (author)

PDGF activates K-Cl cotransport through phosphoinositide 3-kinase and protein phosphatase-1 in primary cultures of vascular smooth muscle cells.

Science.gov (United States)

Zhang, Jing; Lauf, Peter K; Adragna, Norma C

2005-07-15

K-Cl cotransport (K-Cl COT, KCC) is an electroneutrally coupled movement of K and Cl present in most cells. In this work, we studied the pathways of regulation of K-Cl COT by platelet-derived growth factor (PDGF) in primary cultures of vascular smooth muscle cells (VSMCs). Wortmannin and LY 294002 blocked the PDGF-induced K-Cl COT activation, indicating that the phosphoinositide 3-kinase (PI 3-K) pathway is involved. However, PD 98059 had no effect on K-Cl COT activation by PDGF, suggesting that the mitogen-activated protein kinase pathway is not involved under the experimental conditions tested. Involvement of phosphatases was also examined. Sodium orthovanadate, cyclosporin A and okadaic acid had no effect on PDGF-stimulated K-Cl COT. Calyculin A blocked the PDGF-stimulated K-Cl COT by 60%, suggesting that protein phosphatase-1 (PP-1) is a mediator in the PDGF signaling pathway/s. In conclusion, our results indicate that the PDGF-mediated pathways of K-Cl COT regulation involve the signaling molecules PI 3-K and PP-1.

Characterization and determination of efficiency of GM detectors for KCl standards

International Nuclear Information System (INIS)

Priyal, M.R.; Thilagam, L.; Mohapatra, D.K.

2018-01-01

Characterization of Geiger Muller (GM) based beta counters are carried out to determine the main parameters such as plateau slope and efficiency for various slit locations 1 to 10, that are available to keep the sources at different distances away from the detector. Additionally, the disc shaped potassium chloride (KCl) beta standards of various 40 K activities are prepared with variable mass and estimated for the efficiencies of GM tube detectors. The activity of 40K, the counts per second and the efficiency of GM tubes are studied as a function of mass of KCl standards

Detection of Fluorescence for Lanthanides in LiCl-KCl Molten Salt Medium

International Nuclear Information System (INIS)

Im, Hee Jung; Kim, Tack Jin; Song, Kyu Seok; Jee, Kwang Yong

2007-01-01

In the electrorefining step of the pyrochemical process, actinide ions dissolved in the LiCl-KCl eutectic salt are recovered as pure actinide metals at a cathode for a re-use as a nuclear fuel from the aspect of its nonproliferation of the nuclear fuel cycles. The lanthanide species dissolved in the LiCl-KCl eutectic salt play an important role in an effective metal purification during the electrorefining step, so it is necessary to understand the chemical and physical behaviors of lanthanides in molten salt. The in situ spectroscopic measurement system and studies according to temperature changes are essential for better understandable information. To our knowledge, the absorption studies of lanthanides at high temperatures have been reported before, but the fluorescence studies of those at high temperature are not reported yet. We will discuss here the fluorescence behaviors of lanthanides in LiCl-KCl molten salt medium according to a changing temperature

Integrated Data Collection Analysis (IDCA) Program - KClO₄/Aluminum Mixture

Energy Technology Data Exchange (ETDEWEB)

Sandstrom, Mary M. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Brown, Geoffrey W. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Preston, Daniel N. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Pollard, Colin J. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Warner, Kirstin F. [Naval Surface Warfare Center (NSWC IHD), Indian Head, MD (United States). Indian Head Division; Sorensen, Daniel N. [Naval Surface Warfare Center (NSWC IHD), Indian Head, MD (United States). Indian Head Division; Remmers, Daniel L. [Naval Surface Warfare Center (NSWC IHD), Indian Head, MD (United States). Indian Head Division; Whinnery, LeRoy L. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Shelley, Timothy J. [Air Force Research Lab. (AFRL), Tyndall AFB, FL (United States); Reyes, Jose A. [Applied Research Associates (ARA), Tyndall AFB, FL (United States); Hsu, Peter C. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Reynolds, John G. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2012-01-17

The Integrated Data Collection Analysis (IDCA) program is conducting a Proficiency Test for Small-Scale Safety and Thermal (SSST) testing of homemade explosives (HMEs). Described here are the results for impact, friction, electrostatic discharge, and differential scanning calorimetry analysis of a mixture of KClO₄ and aluminum—KClO₄/Al mixture. This material was selected because of the challenge of performing SSST testing of a mixture of two solids. The mixture was found to be: 1) much less sensitive to impact than RDX, (LLNL being the exception) and PETN, 2) more sensitive to friction than RDX and PETN, and 3) extremely sensitive to spark. The thermal analysis showed little or no exothermic character. One prominent endothermic feature was observed in the temperature range studied and identified as a phase transition of KClO₄.

Distillation of LiCl from the LiCl-Li2O molten salt of the electrolytic reduction process

International Nuclear Information System (INIS)

Kim, I.S.; Oh, S.C.; Im, H.S.; Hur, J.M.; Lee, H.S.

2013-01-01

Electrolytic reduction of the uranium oxide in LiCl-Li 2 O molten salt for the treatment of spent nuclear fuel requires the separation of the residual salt from the reduced metal product, which contains about 20 wt% salt. In order to separate the residual salt and reuse it in the electrolytic reduction, a vacuum distillation process was developed. Lab-scale distillation equipment was designed and installed in an argon atmosphere glove box. The equipment consisted of an evaporator in which the reduced metal product was contained and exposed to a high temperature and reduced pressure; a receiver; and a vertically oriented condenser that operated at a temperature below the melting point of lithium chloride. We performed experiments with LiCl-Li 2 O salt to evaluate the evaporation rate of LiCl salt and varied the operating temperature to discern its effect on the behavior of salt evaporation. Complete removal of the LiCl salt from the evaporator was accomplished by reducing the internal pressure to <100 mTorr and heating to 900 deg C. We achieved evaporation efficiency as high as 100 %. (author)

Ionic conductivity studies in crystalline PVA/NaAlg polymer blend electrolyte doped with alkali salt KCl

Science.gov (United States)

Sheela, T.; Bhajantri, R. F.; Ravindrachary, V.; Pujari, P. K.; Rathod, Sunil G.; Naik, Jagadish

2014-04-01

Potassium Chloride (KCl) doped poly(vinyl alcohol) (PVA)/sodium alginate (NaAlg) in 60:40 wt% polymer blend electrolytes were prepared by solution casting method. The complexation of KCl with host PVA/NaAlg blend is confirmed by FTIR and UV-Vis spectra. The XRD studies show that the crystallinity of the prepared blends increases with increase in doping. The dc conductivity increases with increase in dopant concentration. Temperature dependent dc conductivity shows an Arrhenius behavior. The dielectric properties show that both the dielectric constant and dielectric loss increases with increase in KCl doping concentration and decreases with frequency. The cole-cole plots show a decrease in bulk resistance, indicates the increase in ac conductivity, due to increase in charge carrier mobility. The doping of KCl enhances the mechanical properties of PVA/NaAlg, such as Young's modulus, tensile strength, stiffness.

Performance of LiCl Impregnated Mesoporous Material Coating over Corrugated Heat Exchangers in a Solid Sorption Chiller

Directory of Open Access Journals (Sweden)

Hongzhi Liu

2018-06-01

Full Text Available The composite material made by impregnating 40 wt. % lithium chloride (LiCl into the mesopores of a kind of natural porous rock (Wakkanai Siliceous Shale: WSS micropowders (short for “WSS + 40 wt. % LiCl” had been developed previously, and can be regenerated below 100 °C with a cooling coefficient of performance (COP of approximately 0.3 when adopted as a sorbent in a sorption cooler. In this study, experiments have been carried out on an intermittent solid sorption chiller with the WSS + 40 wt. % LiCl coating over two aluminum corrugated heat exchangers. Based on the experimental condition (regeneration temperature of 80 °C, condensation temperature of 30 °C in the desorption process; sorption temperature of 30 °C and evaporation temperature of 12 °C in the sorption process, the water sorption amount changes from 20 wt. % to 70 wt. % in one sorption cooling cycle. Moreover, a specific cooling power (SCP of 86 W/kg, a volumetric specific cooling power (VSCP of 42 W/dm3, and a specific sorption power of 170 W/kg can be achieved with a total sorption and desorption time of 20 min. The obtained cooling COP is approximately 0.16.

Preparation, characterization, biological activity, and transport study of polystyrene based calcium–barium phosphate composite membrane

Energy Technology Data Exchange (ETDEWEB)

Khan, Mohammad Mujahid Ali; Rafiuddin,, E-mail: rafi_amu@rediffmail.com

2013-10-15

Calcium–barium phosphate (CBP) composite membrane with 25% polystyrene was prepared by co-precipitation method. Scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transformed infrared (FTIR), and Thermogravimetric analysis (TGA) were used to characterize the membrane. The membrane was found to be crystalline in nature with consistent arrangement of particles and no indication of visible cracks. The electrical potentials measured across the composite membrane in contact with univalent electrolytes (KCl, NaCl and LiCl), have been found to increase with decrease in concentrations. Thus the membrane was found to be cation-selective. Transport properties of developed membranes may be utilized for the efficient desalination of saline water and more importantly demineralization process. The antibacterial study of this composite membrane shows good results for killing the disease causing bacteria along with waste water treatment. Highlights: • Transport properties of composite membrane are evaluated. • The composite membrane was found to be stable in all media. • TMS method is used for electrochemical characterization. • The membrane was found to be cation selective. • The order of surface charge density was found to be LiCl < NaCl < KCl.

Selective solid-liquid extraction of lithium halide salts using a ditopic macrobicyclic receptor.

Science.gov (United States)

Mahoney, Joseph M; Beatty, Alicia M; Smith, Bradley D

2004-11-29

A ditopic salt receptor that is known to bind and extract solid NaCl, KCl, NaBr, and KBr into organic solution as their contact ion pairs is now shown by NMR and X-ray crystallography to bind and extract solid LiCl and LiBr as water-separated ion pairs. The receptor can transport these salts from an aqueous phase through a liquid organic membrane with a cation selectivity of K+ > Na+ > Li+. However, the selectivity order is strongly reversed when the receptor extracts solid alkali metal chlorides and bromides into organic solution. For a three-component mixture of solid LiCl, NaCl, and KCl, the ratio of salts extracted and complexed to the receptor in CDCl3 was 94:4:2, respectively. The same strong lithium selectivity was also observed in the case of a three-component mixture of solid LiBr, NaBr, and KBr where the ratio of extracted salts was 92:5:3. This observation is attributed to the unusually high solubility of lithium salts in organic solvents. The study suggests that ditopic receptors with an ability to extract solid salts as associated ion pairs may have application in separation processes.

Characterization of glial cell K-Cl cotransport.

Science.gov (United States)

Gagnon, Kenneth B E; Adragna, Norma C; Fyffe, Robert E W; Lauf, Peter K

2007-01-01

The molecular mechanism of K-Cl cotransport (KCC) consists of at least 4 isoforms, KCC 1, 2, 3, and 4 which, in multiple combinations, exist in most cells, including erythrocytes and neuronal cells. We utilized reverse-transcriptase-polymerase chain reaction (RT-PCR) and ion flux studies to characterize KCC activity in an immortalized in vitro cell model for fibrous astrocytes, the rat C6 glioblastoma cell. Isoform-specific sets of oligonucleotide primers were synthesized for NKCC1, KCC1, KCC2, KCC3, KCC4, and also for NKCC1 and actin. K-Cl cotransport activity was determined by measuring either the furosemide-sensitive, or the Cl(-)-dependent bumetanide-insensitive Rb(+) (a K(+) congener) influx in the presence of the Na/K pump inhibitor ouabain. Rb(+) influx was measured at a fixed external Cl concentrations, [Cl(-)](e), as a function of varying external Rb concentrations, [Rb(+)](e), and at a fixed [Rb(+)](e) as a function of varying [Cl(-)](e), and with equimolar Cl replacement by anions of the chaotropic series. RT-PCR of C6 glioblastoma (C6) cells identified mRNA for three KCC isoforms (1, 3, and 4). NKCC1 mRNA was also detected. The apparent K(m) for KCC-mediated Rb(+) influx was 15 mM [Rb(+)](e), and V(max) 12.5 nmol Rb(+) * mg protein(-1) * minute(-1). The calculated apparent K(m) for external Cl(-) was 13 mM and V(max) 14.4 nmol Rb(+) * mg protein(-1) * minute(-1). The anion selectivity sequence of the furosemide-sensitive Rb(+) influx was Cl(-)>Br-=NO(3)(-)>I(-)=SCN(-)>Sfm(-) (sulfamate). Established activators of K-Cl cotransport, hyposmotic shock and N-ethylmaleimide (NEM) pretreatment, stimulated furosemide-sensitive Rb(+) influx. A ñ50% NEM-induced loss of intracellular K(+) was prevented by furosemide. We have identified by RT-PCR the presence of three distinct KCC isoforms (1, 3, and 4) in rat C6 glioblastoma cells, and functionally characterized the anion selectivity and kinetics of their collective sodium-independent cation-chloride cotransport

The electrical conductivity of model melts based on LiCl-KCl, used for the processing of spent nuclear fuel

International Nuclear Information System (INIS)

Salyulev, Alexander; Potapov, Alexei; Khokhlov, Vladimir; Shishkin, Vladimir

2017-01-01

During pyrochemical reprocessing of spent nuclear fuel, complex melts based on LiCl-KCl eutectic are formed, but their properties are still not well studied. We measured the electrical conductivity of (LiCl-KCl) eut. − CeCl 3 , (LiCl-KCl) eut. − NdCl 3 and (LiCl-KCl) eut. − UCl 3 quasi-binary melts was up to 40 mol.% CeCl 3 , 40 mol.% NdCl 3 and 10.45 mol.% UCl 3 in a wide temperature span. In addition the electrical conductivity of several compositions, such as (LiCl-KCl) eut. − CeCl 3 + NdCl 3 and (LiCl-KCl) eut. − CeCl 3 + NdCl 3 + UCl 3 was measured. The measurements were carried out in quartz cells of the capillary type. When the total concentration of trivalent ions is less than 12 mol.%, we found that the conductivity of mixtures of arbitrary composition is almost a linear function of CeCl 3 , NdCl 3 , and UCl 3 the overall concentration.

Respon Pertumbuhan Bibit Kakao (Theobroma Cacao L.) TerhadapPemberian Pupuk Guano Dan KCl

OpenAIRE

Rajagukguk, Pispa; Siagian, Balonggu; Rosanty Lahay, Ratna

2015-01-01

Addition of guano in cultivation of cacao seedling is the one step to use organic fertilizer thatcomes from animal feces and it is used to add soil nutrient for the growth of cocoa seedlings, aswell addition of KCl is used to add soil nutrient too. For that purpose addition guano and KCl aimsto increase growth of cacao in cultivation of seedling. This research had been conducted atexperimental field of agriculture fakulty University of North Sumatera in October 2013 - January2014 using factor...

Study of an F center in molten KCl

International Nuclear Information System (INIS)

Parrinello, M.; Rahman, A.

1983-05-01

It is shown that a discretized version of Feynman's path integral provides a convenient tool for the numerical investigation of the properties of an electron solvated in molten KCl. The binding energy and the pair correlation functions are calculated. The local structure around the solute electron appears to be different from that of an F center in the solid

KCl-induced high temperature corrosion of selected commercial alloys. Part I: chromia-formers

DEFF Research Database (Denmark)

Kiamehr, Saeed; Dahl, Kristian Vinter; Montgomery, Melanie

2015-01-01

-grained), Sanicro 28 and the nickel-based alloys 625, 263 and C276. Exposure was performed at 600 °C for 168 h in flowing N2(g)+5%O2(g)+15% H2O(g) (vol.%). Samples were covered with KCl powder prior to exposure. A salt-free exposure was also performed for comparison. Corrosion morphology and products were studied......Laboratory testing of selected chromia-forming alloys was performed to rank the materials and gain further knowledge on the mechanism of KCl-induced high temperature corrosion. The investigated alloys were stainless steels EN1.4021, EN1.4057, EN1.4521, TP347H (coarse-grained), TP347HFG (fine....... In the presence of solid KCl, all the alloys showed significant corrosion. Measurement of corrosion extent indicated that alloys EN1.4057, Sanicro 28 and 625 show a better performance compared to the industrial state of the art material TP347HFG under laboratory conditions. An additional test was performed...

Density of salt melts containing KF, KCl, K2TaF7 and Ta2O5

International Nuclear Information System (INIS)

Agulyanskij, A.I.; Stangrit, P.T.; Konstantinov, V.I.

1978-01-01

The results of density measurements by hydrostatic weighing are given for molten K 2 TaF 7 - KF, K 2 TaF 7 -KCL, K 2 TaF 7 - KF - KCl and K 2 TaF 7 - KF - KCl - Ta 2 O 5 mixtures depending on their temperature and composition. The density of the last two systems was measured at compositions close to those of commercial electrolytes. The obtained specific volume - composition dependencies show that no interaction is taking place in the mixtures studied. It is, therefore, believed that, in the K 2 TaF 7 - KF melt, tantalum is mainly present as a complex TaF 7 2- ion, and, in the K 2 TaF 7 - KCl mlt, a certain amount of TaF 6 - ions may be formed along with TaF 7 2-

Gamma coloration of mixed crystals of KCl-KBr doped with Pb2+

International Nuclear Information System (INIS)

Cruz Z, E.; Negron, A.; Ramos A, A.; Ramos B, S.; Hernandez A, J.; Jaque, F; Murrieta S, H.

2001-01-01

The amount of the first stage coloration in KCl 1-x Br x doped with Pb 2+ has been investigated as a function of the dose rate and impurity concentration. For a dose rate of 12.88 kGy/h, the F color center production was independent of the quantity of Pb 2+ , and varied according to the ratio KCl/KBr. At a proportion of 50% of each halogen the typical stages were observed. However, if the dose rate is less than 3.22 kGy/h, the coloration production depends on the quantity of Pb 2+ . (author)

Luminescence properties of KCl:Ag{sup -} crystals excited near the fundamental absorption edge

Energy Technology Data Exchange (ETDEWEB)

Kawai, Taketoshi, E-mail: buri@p.s.osakafu-u.ac.jp [Department of Physical Science, Graduate School of Science, Osaka Prefecture University, Gakuen-cho 1-1, Naka-ku, Sakai, Osaka 599-8531 (Japan); Hirai, Takeshi [Department of Physical Science, Faculty of Science and Engineering, Ritsumeikan University, Noji Higashi 1-1-1, Kusatsu, Shiga 525-8577 (Japan)

2012-02-15

Luminescence properties of KCl single crystals doped with Ag{sup -} centers have been investigated under various excitation energies around the fundamental absorption edge at low temperatures. Under the excitation at 6.89 eV, which is lower than the intrinsic exciton energy by 0.87 eV, the A Prime luminescence band due to the intraionic transition in the Ag{sup -} ion is dominantly observed at 2.91 eV. On the other hand, the excitation at 6.66 eV induces a broad luminescence band at 2.60 eV in addition to the A Prime luminescence band. From the comparison with the localized excitons in KCl:I crystals, the 2.60 eV luminescence band is attributed to the two-center type localized exciton related with the Ag{sup -} ion. The adiabatic potential energy surfaces of the excited states in the Ag{sup -} center and the localized exciton in KCl:Ag{sup -} are discussed. - Highlights: Black-Right-Pointing-Pointer We study the luminescence properties of KCl single crystals doped with Ag{sup -} ions. Black-Right-Pointing-Pointer The excitation around the absorption edge induces a broad luminescence at 2.60 eV. Black-Right-Pointing-Pointer The 2.60 eV luminescence is attributed to the exciton localized at the Ag{sup -} ion. Black-Right-Pointing-Pointer The localized exciton has the two-center type configuration of the relaxed exciton.

Study of an F center in molten KCl

Energy Technology Data Exchange (ETDEWEB)

Parrinello, M.; Rahman, A.

1983-05-01

It is shown that a discretized version of Feynman's path integral provides a convenient tool for the numerical investigation of the properties of an electron solvated in molten KCl. The binding energy and the pair correlation functions are calculated. The local structure around the solute electron appears to be different from that of an F center in the solid.

Temperature dependence of diffusion coefficients of trivalent uranium ions in chloride and chloride-fluoride melts

International Nuclear Information System (INIS)

Komarov, V.E.; Borodina, N.P.

1981-01-01

Diffusion coefficients of U 3+ ions are measured by chronopotentiometric method in chloride 3LiCl-2KCl and in mixed chloride fluoride 3LiCl(LiF)-2KCl melts in the temperature range 633-1235 K. It is shown It is shown that experimental values of diffusion-coefficients are approximated in a direct line in lg D-1/T coordinate in chloride melt in the whole temperature range and in chloride-fluoride melt in the range of 644-1040 K. Experimental values of diffusion coefficients diviate from Arrhenius equation in the direction of large values in chloride-fluoride melt at further increase of temperature up to 1235 K. Possible causes of such a diviation are considered [ru

Release of mercury halides from KCl denuders in the presence of ozone

Directory of Open Access Journals (Sweden)

S. N. Lyman

2010-09-01

Full Text Available KCl-coated denuders have become a standard method for measurement of gaseous oxidized mercury, but their performance has not been exhaustively evaluated, especially in field conditions. In this study, KCl-coated and uncoated quartz denuders loaded with HgCl₂ and HgBr₂ lost 29–55% of these compounds, apparently as elemental mercury, when exposed to ozone (range of 6–100 ppb tested. This effect was also observed for denuders loaded with gaseous oxidized mercury at a field site in Nevada (3–37% of oxidized mercury lost. In addition, collection efficiency decreased by 12–30% for denuders exposed to 50 ppb ozone during collection of HgCl₂. While data presented were obtained from laboratory tests and as such do not exactly simulate field sampling conditions, these results indicate that the KCl denuder oxidized mercury collection method may not be as robust as previously thought. This work highlights needs for further testing of this method, clear identification of gaseous oxidized mercury compounds in the atmosphere, and development of field calibration methods for these compounds.

Ionic conductivity in irradiated KCL

International Nuclear Information System (INIS)

Vignolo Rubio, J.

1979-01-01

The ionic conductivity of X and gamma irradiated KCl single crystals has been studied between room temperature and 600 deg C. The radiation induced damage resulting in a decrease of the conductivity heals by thermal annealing in two steps which are at about 350 and 550 deg C respectively. It has been found that the radiation induced colour centres are not involved in the observed decrease of the ionic conductivity. Howewer, it has been observed that the effects of quenching and plastic deformation on the conductivity of the samples are very similar to the effect induced by irradiation. It is suggested that small radiation induced dislocation loops might cause the ionic conductivity decrease observed in irradiated samples. (auth)

Ionic conductivity in irradiated KCL

International Nuclear Information System (INIS)

Vignolo Rubio, J.

1979-01-01

The ionic conductivity of X and gamma irradiated KCL single crystals has been studied between room temperature and 600 degree centigree. the radiation induced damage resulting in a decrease of the conductivity heals by thermal annealing in two steps which are at about 350 and 550 degree centigree respectively. It has been found that the radiation induced colour centres are not involved in the observed decrease of the ionic conductivity. However. It has been observed that the effects of quenching and plastic deformation on the conductivity of the samples are very similar to the effect induced by irradiation. It is suggested that, samples radiation induced dislocation loops might cause the ionic conductivity decrease observed in irradiated samples. (Author)

Partitioning of actinides and fission products using molten salt electrorefining process

International Nuclear Information System (INIS)

Barbero, Jose A.; Wiesztort, Andres; Azcona, Alejandra; Bollini, Edgardo; Forchetti, Alberto; Orce, Alan

1999-01-01

Electrorefining is the key step of pyrometallurgical processing for separating actinides from fission products. In this work, the electrorefining process is carried out in a electrorefining cell that contains molten salts (49% LiCl- 51% KCL) floating on a liquid cadmium. The cell is operated under an inert atmosphere at 500 degree C. In this work we describe in detail the construction of the cell and the way of operation

LiCl Dehumidifier LiBr absorption chiller hybrid air conditioning system with energy recovery

Science.gov (United States)

Ko, Suk M.

1980-01-01

This invention relates to a hybrid air conditioning system that combines a solar powered LiCl dehumidifier with a LiBr absorption chiller. The desiccant dehumidifier removes the latent load by absorbing moisture from the air, and the sensible load is removed by the absorption chiller. The desiccant dehumidifier is coupled to a regenerator and the desiccant in the regenerator is heated by solar heated hot water to drive the moisture therefrom before being fed back to the dehumidifier. The heat of vaporization expended in the desiccant regenerator is recovered and used to partially preheat the driving fluid of the absorption chiller, thus substantially improving the overall COP of the hybrid system.

Electrode processes during the electrorefiniment of lead in the KCl-PbCl2-PbO melt

Directory of Open Access Journals (Sweden)

P. S. Pershin

2015-03-01

Full Text Available The influence of PbO addition on current efficiency during the electrorefinement of lead in the KCl-PbCl2-PbO melt was investigated. It was shown that with PbO concentration in the KCl-PbCl2 eqiumolar mixture increasing, the current efficiency of lead decreases. Electrode processes mechanism is proposed.

Acidity of cations and the solubility of oxides in the eutectic KCl-LiCl melt at 700 Deg C

International Nuclear Information System (INIS)

Cherginets, V.L.; Rebrova, T.P.

1999-01-01

Products of MgO, NiO and CoO solubility in KCl-LiCl melt at 700 Deg C were determined by the method of potentiometric titration using Pt(O 2 )IZrO 2 (Y 2 O 3 ) membrane oxygen electrode. It was ascertained that acid properties of Cd 2+ and Pb'2 + cations are levelled to Li + properties, a break in E-pO graduation dependence in KCl-LiCl melt was observed at pO ∼ 2. Increase in oxides solubility in the melt studied compared with KCl-NaCl and CsCl-KCl-NaCl melts stems from the presence of Li + cations in the melt studied, which possess stronger acid properties than those of Na + or K + [ru

Influence of partial replacement of NaCl with KCl on profiles of volatile compounds in dry-cured bacon during processing.

Science.gov (United States)

Wu, Haizhou; Zhuang, Hong; Zhang, Yingyang; Tang, Jing; Yu, Xiang; Long, Men; Wang, Jiamei; Zhang, Jianhao

2015-04-01

This study investigated the influence of partial substitution of NaCl with KCl on the formation of volatile compounds in bacons during processing using a purge and trap dynamic headspace GC/MS system. Three substitutions were 0% KCl (I), 40% KCl (II), and 70% KCl (III). The profiles of the volatile compounds significantly changed during processing, particularly during the drying/ripening. At the end of process, the bacons from substitution III formed significantly higher levels of lipid-derived volatiles, such as straight chain aldehydes, hydrocarbons than bacons from substitution I and II, whereas the latter formed higher levels of volatiles from amino acid degradation such as 3-methylbutanal. There were very few differences in volatile formation between 0% and 40% KCl application. These results suggest that K(+) substitution of Na(+) by more than 40% may significantly change profiles of volatiles in finished dry-cured bacons and therefore would result in changes in the product aroma and/or flavour. Copyright © 2014 Elsevier Ltd. All rights reserved.

The system K2NbF7-K2TiF6-KCl

International Nuclear Information System (INIS)

Kamenskaya, L.A.; Matveev, A.M.

1984-01-01

Using visual-polythermal and thermographical methods the ternary system K 2 NbF 7 -K 2 TiE 6 -KCl has been studied. Crystallization fields of initial components and the field of solid solutions of double compounds K 3 NbClF 7 and K 3 TiClF 6 are outlined. Ternary eutectics at 654 deg C, having the composition K 2 NbF 6 -41, K 2 TiP 6 -41, KCl-18 mol.%, is determined. Potassium fluoroniobate and fluorotitanate form continuous solid solutions unstable in the presence of the third component, potassium chloride

Temperature and salt addition effects on the solubility behaviour of some phenolic compounds in water

International Nuclear Information System (INIS)

Noubigh, Adel; Abderrabba, Manef; Provost, Elise

2007-01-01

Solubility-temperature dependence data for six phenolic compounds (PhC), contained in olive mill wastewater (OMWW), in water and in some chloride salts (KCl, NaCl, and LiCl) aqueous solutions have been presented and solution standard molar enthalpies (Δ sol H 0 ) were determined using Van't Hoff plots. The temperature was varied from 293.15 K to 318.15 K. Solubility data were estimated using a thermostated reactor and HPLC analysis. It has been observed that solubility, in pure water and in aqueous chloride solutions, increases with increasing temperature. The salting-out LiCl > NaCl > KCl order obtained at 298.15 K is confirmed. Results were interpreted in terms of the salt hydration shells and the ability of the solute to form hydrogen-bond with water. The standard molar Gibbs free energies of transfer of PhC (Δ tr G 0 ) from pure water to aqueous solutions of the chloride salts have been calculated from the solubility data. In order to estimate the contribution of enthalpic and entropic terms, standard molar enthalpies (Δ tr H 0 ) and entropies (Δ tr S 0 ) of transfer have also been calculated. The decrease in solubility is correlated to the positive Δ tr G 0 value which is mainly of enthalpic origin

Molecular-resolution imaging of pentacene on KCl(001

Directory of Open Access Journals (Sweden)

Julia L. Neff

2012-02-01

Full Text Available The growth of pentacene on KCl(001 at submonolayer coverage was studied by dynamic scanning force microscopy. At coverages below one monolayer pentacene was found to arrange in islands with an upright configuration. The molecular arrangement was resolved in high-resolution images. In these images two different types of patterns were observed, which switch repeatedly. In addition, defects were found, such as a molecular vacancy and domain boundaries.

Balanço de potássio e desempenho de frangos de corte suplementados com KCl no verão Potassium balance and performance of broilers supplemented with KCl in summer

Directory of Open Access Journals (Sweden)

Bonifácio Benicio de Souza

2004-10-01

Full Text Available Objetivou-se com o presente trabalho avaliar o efeito da suplementação de cloreto de potássio (KCl sobre o balanço de potássio e o desempenho de frangos de corte no verão. Foram utilizados 288 frangos de corte, da linhagem Hubbard, sexados, alojados em baterias no período de 28 a 49 dias de idade, distribuídos segundo um delineamento inteiramente casualizado em esquema fatorial 6 x 2, com 6 níveis de KCl (0,0; 0,4; 0,8; 1,2; 1,6; 2,0% e 2 sexos, com 4 repetições de 6 aves cada uma. As temperaturas máxima e mínima, umidade relativa do ar e o índice de temperatura do globo negro e umidade (ITGU, durante o período experimental, foram de 31,5ºC e 20,5ºC, 68% e 77%, respectivamente. As aves receberam ração "ad libitum", com dietas formuladas à base de milho e farelo de soja. Quando as aves atingiram a idade de 35 dias, foi realizado o balanço de potássio, durante um período de 96 horas. A elevação na suplementação de KCl na dieta aumentou linearmente (PThis experiment was conducted to verify the effect of KCl on potassium balance and performance of broilers in summer. A total of 288 broiler chickens aged 28 to 49 days was utilized, allocated according to a completely randomized design in a 6 x 2 factorial scheme 6 levels of KCl (0,0; 0,4; 0,8; 1,2; 1,6; 2,0 % and 2 sexes, with four replications of 6 birds each. The maximum and minimum temperatures, relative humidity and black globe-humidity index (BGHI were of 31,5ºC and 20ºC, 68% and of 73%, respectability. With the growing supplementation of KCl, there was a linear increase (P<0.01 in the intake, excretion and retention of the potassium, concentration of potassium in the plasma and water consumption. There was a linear reduction (P<0.01 of the excreta dry matter. The males overcame the females (P<0.01 in the intake and excretion of potassium. However, the females overcame the males (P<0.01 in the retention of the potassium. There was a positive balance of potassium for

Modeling electronic defects in La2CuO4 and LiCl using embedded quantum cluster methodology

International Nuclear Information System (INIS)

Grimes, R.W.; Shluger, A.L.; Baetzold, R.; Catlow, C.R.A.

1991-01-01

By exploiting recent developments in computer simulation methods the authors modeled the behavior of hole states in La 2 CuO 4 and excited state defects such as the exciton in LiCl. The authors methodology employs a Hartree-Fock cluster embedded in a classical surround. Although the method is discussed with respect to the hole and exciton defects in particular, the scope of the talk includes other material problems currently being investigated by this method. Thus, the types of problems for which the method are appropriate are illustrated and the present limitations are discussed

Reactive scattering from oriented molecules: The three-center reaction K+ICl --> KI+Cl, KCl+I

Science.gov (United States)

Loesch, H. J.; Möller, J.

1992-12-01

In a crossed molecular beam experiment, we have measured the angular and time-of-flight (TOF) distributions of the products KCl and KI formed in the reaction K+ICl→KI+Cl, KCl+I at an elevated collision energy of Etr=1.64 eV. Employing the brute force method, we have prepared an oriented ICl beam and studied in addition also the orientation dependence of these distributions. The results are (i) KCl is the dominant product, but also KI is substantially formed with a branching ratio of 4:1; (ii) the double differential reaction cross section in the center-of-mass frame (contour maps) indicates that all products are preferentially forward scattered and constrained to the forward hemisphere; (iii) the KCl flux consists of two distinct components which differ markedly in kinetic energy and dependence on the ICl orientation; there are also indications of the existence of two components of KI; (iv) 65%, 84%, and 64% of the available energy is vested into the internal degrees of freedom for the fast, slow component of KCl and KI, respectively; (v) the existence of two components can be rationalized on the basis of the harpooning mechanism where the jumping electron accesses the ground state or one of the low excited states of the ICl- ion and triggers the subsequent explosion of the ion with more or less kinetic energy of the fragments depending on the initially populated state; (vi) the energies released during dissociation of ICl- in the 2Σ ground state and the first 2Π state are ≤0.19 and ≤1.2 eV, respectively; (vii) the fast KCl component features a negative steric effect suggesting favorable product formation for attacks of K to the I end of ICl, the steric effect of the slow KI component is positive, i.e., attacks to the Cl end form products favorably; the other components exhibit no significant steric effect; (viii) the steric effects can be quantitatively rationalized using the same model as mentioned above; (ix) the magnitude of the steric effect suggests a

Release and transformation of chlorine and potassium during pyrolysis of KCl doped biomass

DEFF Research Database (Denmark)

Wang, Yang; Wu, Hao; Sárossy, Zsuzsa

2017-01-01

–850 °C), and KCl contents (0–5 wt%). The volatiles were collected and analyzed for CH3Cl concentration by GC–MS. The solid residue was analyzed by ICP-OES for the contents of total and water soluble K and Cl. Considerable amounts of CH3Cl, corresponding to 20–50% of the fuel chlorine, were formed......The formation of CH3Cl and the transformation of chlorine and potassium during pyrolysis of biomass were investigated. Model biomass compounds (cellulose, xylan, lignin and pectin) and pine wood doped with KCl were pyrolysed in a TGA at different heating rates (10–1000 °C/min), temperatures (300...

Potential Process for the Decontamination of Pyro-electrometallurgical LiCl-KCl Eutectic Salt Electrolyte

International Nuclear Information System (INIS)

Griffith, Christopher S.; Sizgek, Erden; Sizgek, Devlet; Luca, Vittorio

2008-01-01

Presented here is a potential option with experimental validation for the decontamination of LiCl-KCl eutectic salt electrolyte from a pyro-electrometallurgical process by employing already developed inorganic ion exchange materials. Adsorbent materials considered include titano-silicates and molybdo- and tungstophosphates for Cs extraction, Si-doped antimony pyrochlore for Sr extraction and hexagonal tungsten bronzes for lanthanide (LN) and minor actinide (MA) polishing. Encouraging results from recent investigations on the removal of target elements (Cs, Sr and LN) from aqueous solutions containing varying concentrations of alkali and alkali metal contaminants which would be akin to a solution formed from the dissolution of spent LiCl-KCl eutectic salt electrolyte are presented. Further investigations have also shown that the saturated adsorbents can be treated at relatively low temperatures to afford potential waste forms for the adsorbed elements. Efficient evaporation and drying of a solution of dissolved LiCl-KCl eutectic salt electrolyte (50 L, 5 L.h -1 ) has been demonstrated using a Microwave-Heated Mechanical Fluidized Bed (MWMFB) apparatus. (authors)

Potential Process for the Decontamination of Pyro-electrometallurgical LiCl-KCl Eutectic Salt Electrolyte

Energy Technology Data Exchange (ETDEWEB)

Griffith, Christopher S.; Sizgek, Erden; Sizgek, Devlet; Luca, Vittorio [Australian Nuclear Science and Technology Organisation (ANSTO), Institute of Materials Engineering, New Illawarra Road, Lucas Heights, New South Wales, 2234 (Australia)

2008-07-01

Presented here is a potential option with experimental validation for the decontamination of LiCl-KCl eutectic salt electrolyte from a pyro-electrometallurgical process by employing already developed inorganic ion exchange materials. Adsorbent materials considered include titano-silicates and molybdo- and tungstophosphates for Cs extraction, Si-doped antimony pyrochlore for Sr extraction and hexagonal tungsten bronzes for lanthanide (LN) and minor actinide (MA) polishing. Encouraging results from recent investigations on the removal of target elements (Cs, Sr and LN) from aqueous solutions containing varying concentrations of alkali and alkali metal contaminants which would be akin to a solution formed from the dissolution of spent LiCl-KCl eutectic salt electrolyte are presented. Further investigations have also shown that the saturated adsorbents can be treated at relatively low temperatures to afford potential waste forms for the adsorbed elements. Efficient evaporation and drying of a solution of dissolved LiCl-KCl eutectic salt electrolyte (50 L, 5 L.h{sup -1}) has been demonstrated using a Microwave-Heated Mechanical Fluidized Bed (MWMFB) apparatus. (authors)

A reactive distillation process for the treatment of LiCl-KCl eutectic waste salt containing rare earth chlorides

Energy Technology Data Exchange (ETDEWEB)

Eun, H.C., E-mail: ehc2004@kaeri.re.kr; Choi, J.H.; Kim, N.Y.; Lee, T.K.; Han, S.Y.; Lee, K.R.; Park, H.S.; Ahn, D.H.

2016-11-15

The pyrochemical process, which recovers useful resources (U/TRU metals) from used nuclear fuel using an electrochemical method, generates LiCl-KCl eutectic waste salt containing radioactive rare earth chlorides (RECl{sub 3}). It is necessary to develop a simple process for the treatment of LiCl-KCl eutectic waste salt in a hot-cell facility. For this reason, a reactive distillation process using a chemical agent was achieved as a method to separate rare earths from the LiCl-KCl waste salt. Before conducting the reactive distillation, thermodynamic equilibrium behaviors of the reactions between rare earth (Nd, La, Ce, Pr) chlorides and the chemical agent (K{sub 2}CO{sub 3}) were predicted using software. The addition of the chemical agent was determined to separate the rare earth chlorides into an oxide form using these equilibrium results. In the reactive distillation test, the rare earth chlorides in LiCl-KCl eutectic salt were decontaminated at a decontamination factor (DF) of more than 5000, and were mainly converted into oxide (Nd{sub 2}O{sub 3}, CeO{sub 2}, La{sub 2}O{sub 3}, Pr{sub 2}O{sub 3}) or oxychloride (LaOCl, PrOCl) forms. The LiCl-KCl was purified into a form with a very low concentration (<1 ppm) for the rare earth chlorides.

KCl-induced high temperature corrosion of selected commercial alloys. Part II: alumina and silica-formers

DEFF Research Database (Denmark)

Kiamehr, Saeed; Dahl, Kristian Vinter; Montgomery, Melanie

2016-01-01

for 168 h in flowing N2(g)+5%O2(g)+15%H2O(g) (vol.%) with samples covered under KCl powder. A KCl-free exposure was also performed for comparison.Corrosion morphology and products were studied with scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and X-ray diffractometry (XRD......Laboratory testing on selected alumina and silica-forming alloys was performed to evaluate their performance against high temperature corrosion induced by potassium chloride (KCl). The alloys studied were FeCrAlY, Kanthal APM, Nimonic 80A, 214, 153MA and HR160. Exposure was conducted at 600 °C......-chromium-silicon-oxygen containing layer forms as the innermost corrosion product. The layer was uniformly distributed over the surface and appears to render some protection as this alloy exhibited the best performance among the investigated alloys. To reveal further aspects of the corrosion mechanism, Nimonic 80A was exposed...

X-ray or UV-ray imaging sensor utilizing optically stimulated luminescence phenomenon in Eu-doped KCl phosphors

International Nuclear Information System (INIS)

Nanto, Hidehito; Murayama, Kazuhiko; Hirai, Yoshiaki; Taniguchi, Shin-ichi; Makamura, Shouichi; Takeuchi, Nozomu.

1993-01-01

An intense OSL with a peak at about 420 [nm] has been observed by stimulating an X-ray or UV-ray irradiated KCl: Eu crystal with F-band light whose wavelength is about 560 [um]. A possible excitation and emission mechanisms for the 420 [um] OSL peak X-ray or UV-ray irradiated sample is proposed. It is found that the OSL intensity is proportional to the X-ray absorbed dose or UV-ray irradiation dose. It is also found that X-ray or UV-ray irradiated KCl; Eu exhibited excellent fading characteristics. These results strongly suggest that the KCl: Eu is one of the most attractive candidates for two-dimensional X-ray or UV-ray imaging sensor utilizing the OSL phenomenon. (J.P.N.)

Research on Wetting-Drying Cycles’ Effect on the Physical and Mechanical Properties of Expansive Soil Improved by OTAC-KCl

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Bao-tian Wang

2015-01-01

Full Text Available Expansive soil experiences periodic swelling and shrinkage during the alternate wet and dry environments, which will result in severe damage to the slope stability. In this study, a promising modifier OTAC-KCl is introduced, which has a good diffusivity and is soluble in water or other solvents easily. Firstly, a reasonable combination of ameliorant 0.3% STAC and 3% KCl is chosen referring to the free swell test. Then, the best curing period, 14 days, is gotten from UCS tests. The effect of wetting and drying cycles on engineering properties of expansive soil improved by OTAC-KCl admixtures after 14-day curing is also studied accordingly. Both treated and untreated expansive soil samples are prepared for the cyclic wetting-drying tests which mainly include cyclic swelling potential and cyclic strength tests. Experimental results show that the swelling potential of expansive soil samples stabilized with OTAC-KCl is suppressed efficiently, and the untreated soil specimens will collapse when immersed in water while the treated specimens keep in good conditions. Moreover, expansive soil samples modified with 0.3% OTAC + 3% KCl show enough durability on the swelling ability, shear strength, and unconfined compressive strength, which means, that both the physical and the mechanical properties of stabilized expansive soil have been improved effectively.

Characterization of pack cemented Ni₂Al₃ coating exposed to KCl(s) induced corrosion at 600 °C

DEFF Research Database (Denmark)

Dahl, Kristian Vinter; Slomian, A.; Lomholt, Trine Nybo

2018-01-01

Ni2Al3 shows minimal weight gain, while adding KCl results in a small weight loss consistent with evaporation of KCl. On the surface of samples exposed to the gas environment only, a 30 nm oxide of Al oxide was present, but where KCl was present as deposit, 50–250 nm thick nodules form...

On the influence of alkali metal- and alkaline earth metal chlorides on the rate on inhibition of cholinesterases by organic phosphorus inhibitors

International Nuclear Information System (INIS)

Brestkin, A.P.; Shataeva, G.A.

1975-01-01

Influence of LiCl, NaCl, KCl, RbCl, CsCl, MgCl 2 , CaCl 2 , CrCl 2 , BaCl 2 on bimolecular constant (K 2 ) of the interaction rate of acetylcholinesterazo (ACE) and butylcholinesterazo (BuCE) with phosphororganic inhibitors was studied. K 2 value with increasing of the electrolite concentration for the interaction of ACE and BuCE with charged inhibitor is significantly decreased and significantly increased in case of interaction with neutral inhibitor

A simple and rapid nucleic acid preparation method for reverse ...

African Journals Online (AJOL)

detergent (0.5% Triton XL-80 N) buffers, vortexed for 3 min and then 2.5 ìl of this aliquots was used in RT-PCR. Alternatively, evaluation of the efficiency of different buffers (sodium sulphite buffer, 0.1 M HCl, 0.1 M NaOH, 0.1 M Tris, 0.1 M EDTA, 0.1 M phosphate buffer, 0.1 M LiCl, 0.1 M KCl, 1 M NaCl and water (H2O)) was ...

Hemispherand-Strapped Calix[4]pyrrole: An Ion-pair Receptor for the Recognition and Extraction of Lithium Nitrite.

Science.gov (United States)

He, Qing; Zhang, Zhan; Brewster, James T; Lynch, Vincent M; Kim, Sung Kuk; Sessler, Jonathan L

2016-08-10

The hemispherand-strapped calix[4]pyrrole (1) acts as an ion pair receptor that exhibits selectivity for lithium salts. In organic media (CD2Cl2 and CD3OD, v/v, 9:1), receptor 1 binds LiCl with high preference relative to NaCl, KCl, and RbCl. DFT calculations provided support for the observed selectivity. Single crystal structures of five different lithium ion-pair complexes of 1 were obtained. In the case of LiCl, a single bridging water molecule between the lithium cation and chloride anion was observed, while tight contact ion pairs were observed in the case of the LiBr, LiI, LiNO3, and LiNO2 salts. Receptor 1 proved effective as an extractant for LiNO2 under both model solid-liquid and liquid-liquid extraction conditions.

Porcine proximal tubular cells (LLC-PK1) are able to tolerate high levels of lithium chloride in vitro: assessment of the influence of 1-20 mM LiCl on cell death and alterations in cell biology and biochemistry.

Science.gov (United States)

Lucas, Kirsten C; Hart, David A; Becker, Rolf W

2010-01-25

Lithium, a prophylactic drug for the treatment of bipolar disorder, is prescribed with caution due to its side effects, including renal damage. In this study porcine LLC-PK1 renal tubular cells were used to establish the direct toxicity of lithium on proximal cells and gain insights into the molecular mechanisms involved. In the presence of LiCl, cell proliferation exhibited insignificant decreases in a concentration-dependent manner, but once confluent, constant cell numbers were observed. Cell cycle studies indicated a small dose-dependent accumulation of cells in the G2/M stage after 24 h, as well as an increase in cells in the G0/G1 phase after treatment with 1-10 mM LiCl, but not at 20 mM LiCl. No evidence of apoptosis was observed based on cell morphology or DNA fragmentation studies, or evidence of protein expression changes for Bax, Bcl-2, and p53 proteins using immunocytochemistry. In addition caspases 3, 8 and 9 activity remained unaltered between control and lithium-treated cultures. To conclude, exposure to high concentrations of lithium did not result in overt toxic effects to LLC-PK1 renal cells, although LiCl did alter some aspects of cell behaviour, which could potentially influence function over time.

A spectroscopic study of uranium species formed in chloride melts

International Nuclear Information System (INIS)

Volkovich, Vladimir A.; Bhatt, Anand I.; May, Iain; Griffiths, Trevor R.; Thied, Robert C.

2002-01-01

The chlorination of uranium metal or uranium oxides in chloride melts offers an acceptable process for the head-end of pyrochemical reprocessing of spent nuclear fuels. The reactions of uranium metal and ceramic uranium dioxide with chlorine and with hydrogen chloride were studied in the alkali metal chloride melts, NaCl-KCl at 973K, NaCl-CsCl between 873 and 923K and LiCl-KCl at 873K. The uranium species formed therein were characterized from their electronic absorption spectra measured in situ. The kinetic parameters of the reactions depend on melt composition, temperature and chlorinating agent used. The reaction of uranium dioxide with oxygen in the presence of alkali metal chlorides results in the formation of alkali metal uranates. A spectroscopic study, between 723 and 973K, on their formation and their solutions was undertaken in LiCl, LiCl-KCl eutectic and NaCl-CsCl eutectic melts. The dissolution of uranium dioxide in LiCl-KCl eutectic at 923K containing added aluminium trichloride in the presence of oxygen has also been investigated. In this case, the reaction leads to the formation of uranyl chloride species. (author)

Electrochemical formation of uranium-zirconium alloy in LiCl-KCl melts

Energy Technology Data Exchange (ETDEWEB)

Murakami, Tsuyoshi, E-mail: m-tsuyo@criepi.denken.or.j [Central Research Institute of Electric Power Industry (CRIEPI), Komae-shi, Tokyo 201-8511 (Japan); Kato, Tetsuya; Kurata, Masaki [Central Research Institute of Electric Power Industry (CRIEPI), Komae-shi, Tokyo 201-8511 (Japan); Yamana, Hajimu [Research Reactor Institute, Kyoto University, Kumatori-cho, Sennan-gun, Osaka 590-0494 (Japan)

2009-11-15

Since zirconium is considered an electrochemically active species under practical conditions of the electrorefining process, it is crucial to understand the electrochemical behavior of zirconium in LiCl-KCl melts containing actinide ions. In this study, the electrochemical codeposition of uranium and zirconium on a solid cathode was performed. It was found that the delta-(U, Zr) phase, which is the only intermediate phase of the uranium-zirconium binary alloy system, was deposited on a tantalum substrate by potentiostatic electrolysis at -1.60 V (vs. Ag{sup +}/Ag) in LiCl-KCl melts containing 0.13 in mol% UCl{sub 3} and 0.23 in mol% ZrCl{sub 4} at 773 K. To our knowledge, this is the first report on the electrochemical formation of the delta-(U, Zr) phase. The relative partial molar properties of uranium in the delta-(U, Zr) phase were evaluated by measuring the open-circuit-potentials of the electrochemically prepared delta-phase electrode.

Electrochemical formation of uranium-zirconium alloy in LiCl-KCl melts

International Nuclear Information System (INIS)

Murakami, Tsuyoshi; Kato, Tetsuya; Kurata, Masaki; Yamana, Hajimu

2009-01-01

Since zirconium is considered an electrochemically active species under practical conditions of the electrorefining process, it is crucial to understand the electrochemical behavior of zirconium in LiCl-KCl melts containing actinide ions. In this study, the electrochemical codeposition of uranium and zirconium on a solid cathode was performed. It was found that the δ-(U, Zr) phase, which is the only intermediate phase of the uranium-zirconium binary alloy system, was deposited on a tantalum substrate by potentiostatic electrolysis at -1.60 V (vs. Ag + /Ag) in LiCl-KCl melts containing 0.13 in mol% UCl 3 and 0.23 in mol% ZrCl 4 at 773 K. To our knowledge, this is the first report on the electrochemical formation of the δ-(U, Zr) phase. The relative partial molar properties of uranium in the δ-(U, Zr) phase were evaluated by measuring the open-circuit-potentials of the electrochemically prepared δ-phase electrode.

Thermoluminescence of KCl:Eu2+ under ultraviolet irradiation at different temperatures

International Nuclear Information System (INIS)

Aguirre de Carcer, I.; Jaque, F.; Rowlands, A.P.; Townsend, P.D.

1998-01-01

The thermoluminescence of KCl:Eu 2+ ultraviolet irradiated samples has been studied at different temperatures with the aim of optimising its solar dosimetric characteristics. This was achieved by recording with a dosimeter -10 deg. C. Ultraviolet light (254 nm) irradiation under these conditions produces a high TL peak at 90 deg. C which is linear with exposure time over at least four orders of magnitude. The TL emission spectra of KCl:Eu 2+ under UV irradiation have been analysed to reveal component bands at 2.86 eV, 2.97 eV, 3.02 eV, 3.07 eV, 3.14 eV and 3.26 eV that corresponds to divalent europium impurity sites. The new peak at 3.26 eV (297 nm) had not reported before but it has to be considered in order to match the experimental TL emission. A model for the defect site of this new emission is discussed

Feasibility of Th-U separation through a pyrochemical route in molten LiCl-KCl eutectic

International Nuclear Information System (INIS)

Pakhui, Gurudas; Ghosh, Suddhasattwa; Prabhakara Reddy, B.; Nagarajan, K.

2014-01-01

Molten salt electrorefining is a high temperature electrometallurgical process developed for the reprocessing of spent UPu-Zr fuel employing LiCl-KCl as the electrolyte. A possible application of this high temperature electrochemical process could be in the separation of U from Th matrix for Th based fuels. It therefore becomes important to investigate the reduction behaviour of Th 4+ in the molten salt and compare with that of U 3+ . The present study is on the electrochemical behaviour of Th 4+ in LiCl-KCl. Electrochemical studies were also carried out on the LiCl-KCl-UCl 3 -ThCl 4 system using transient electrochemical techniques. The cyclic voltammograms for Th 4+ /Th redox couple at various scan rates at 723 K is shown. Reduction of Th 4+ to Th was found to be quasi-reversible at lower scan rates and irreversible at higher scan rates using cyclic voltammetry and convolution voltammetry. The number of electrons transferred for the reduction process was calculated to be ∼ 4 using various techniques like cyclic voltammetry, chronopotentiometry and convolution voltammetry

Densities of L-Glutamic Acid HCl Drug in Aqueous NaCl and KCl Solutions at Different Temperatures

Science.gov (United States)

Ryshetti, Suresh; Raghuram, Noothi; Rani, Emmadi Jayanthi; Tangeda, Savitha Jyostna

2016-04-01

Densities (ρ ) of (0.01 to 0.07) {mol}{\\cdot } {kg}^{-1} L-Glutamic acid HCl (L-HCl) drug in water, and in aqueous NaCl and KCl (0.5 and 1.0) {mol}{\\cdot } {kg}^{-1} solutions have been reported as a function of temperature at T = (298.15, 303.15, 308.15, and 313.15) K and atmospheric pressure. The accurate density (ρ ) values are used to estimate the various parameters such as the apparent molar volume (V_{2,{\\upphi }}), the partial molar volume (V2^{∞}), the isobaric thermal expansion coefficient (α 2), the partial molar expansion (E2^{∞}), and Hepler's constant (partial 2V2^{∞}/partial T2)P. The Cosphere overlap model is used to understand the solute-solvent interactions in a ternary mixture (L-HCl drug + NaCl or KCl + water). Hepler's constant (partial 2V2^{∞}/partial T2)_P is utilized to interpret the structure-making or -breaking ability of L-HCl drug in aqueous NaCl and KCl solutions, and the results are inferred that L-HCl drug acts as a structure maker, i.e., kosmotrope in aqueous NaCl solutions and performs as a structure breaker, i.e., chaotrope in aqueous KCl solutions.

Short-pulse CO2-laser damage studies of NaCl and KCl windows

International Nuclear Information System (INIS)

Newnam, B.E.; Nowak, A.V.; Gill, D.H.

1979-01-01

The damage resistance of bare surfaces and the bulk interior of NaCl and KCl windows was measured with a short-pulse CO 2 laser at 10.6 μm. Parametric studies with 1.7-ns pulses indicated that adsorbed water was probably the limiting agent on surface thresholds in agreement with previous studies at long pulsewidths. Rear-surface thresholds up to 7 J/cm 2 were measured for polished NaCl windows, whereas KCl surfaces damaged at approximately 60% of this level. The breakdown electric-field thresholds of exit surfaces were only 50% of the value of the bulk materials. The pulsewidth dependence of surface damage from 1 to 65 ns, in terms of incident laser fluence, increased as t/sup 1/3/

Uncertainties of Gaseous Oxidized Mercury Measurements Using KCl-Coated Denuders, Cation-Exchange Membranes, and Nylon Membranes: Humidity Influences.

Science.gov (United States)

Huang, Jiaoyan; Gustin, Mae Sexauer

2015-05-19

Quantifying the concentration of gaseous oxidized mercury (GOM) and identifying the chemical compounds in the atmosphere are important for developing accurate local, regional, and global biogeochemical cycles. The major hypothesis driving this work was that relative humidity affects collection of GOM on KCl-coated denuders and nylon membranes, both currently being applied to measure GOM. Using a laboratory manifold system and ambient air, GOM capture efficiency on 3 different collection surfaces, including KCl-coated denuders, nylon membranes, and cation-exchange membranes, was investigated at relative humidity ranging from 25 to 75%. Recovery of permeated HgBr2 on KCl-coated denuders declined by 4-60% during spikes of relative humidity (25 to 75%). When spikes were turned off GOM recoveries returned to 60 ± 19% of permeated levels. In some cases, KCl-coated denuders were gradually passivated over time after additional humidity was applied. In this study, GOM recovery on nylon membranes decreased with high humidity and ozone concentrations. However, additional humidity enhanced GOM recovery on cation-exchange membranes. In addition, reduction and oxidation of elemental mercury during experiments was observed. The findings in this study can help to explain field observations in previous studies.

Temperature and salt addition effects on the solubility behaviour of some phenolic compounds in water

Energy Technology Data Exchange (ETDEWEB)

Noubigh, Adel [Laboratoire de Physico-chimie des materiaux, IPEST, BP51, 2070 La MARSA (Tunisia)]. E-mail: Adel.anoubigh@ipest.rnu.tn; Abderrabba, Manef [Laboratoire de Physico-chimie des materiaux, IPEST, BP51, 2070 La MARSA (Tunisia); Provost, Elise [Laboratoire Chimie et procedes, ENSTA, 32 Rue de Boulevard Victor, 75739 Paris, Cedex 15 (France)

2007-02-15

Solubility-temperature dependence data for six phenolic compounds (PhC), contained in olive mill wastewater (OMWW), in water and in some chloride salts (KCl, NaCl, and LiCl) aqueous solutions have been presented and solution standard molar enthalpies ({delta}{sub sol} H {sup 0}) were determined using Van't Hoff plots. The temperature was varied from 293.15 K to 318.15 K. Solubility data were estimated using a thermostated reactor and HPLC analysis. It has been observed that solubility, in pure water and in aqueous chloride solutions, increases with increasing temperature. The salting-out LiCl > NaCl > KCl order obtained at 298.15 K is confirmed. Results were interpreted in terms of the salt hydration shells and the ability of the solute to form hydrogen-bond with water. The standard molar Gibbs free energies of transfer of PhC ({delta}{sub tr} G {sup 0}) from pure water to aqueous solutions of the chloride salts have been calculated from the solubility data. In order to estimate the contribution of enthalpic and entropic terms, standard molar enthalpies ({delta}{sub tr} H {sup 0}) and entropies ({delta}{sub tr} S {sup 0}) of transfer have also been calculated. The decrease in solubility is correlated to the positive {delta}{sub tr} G {sup 0} value which is mainly of enthalpic origin.

Enhancement in CO2 Adsorption Capacity and Selectivity in the Chalcogenide Aerogel CuSb2S4 by Post-synthetic Modification with LiCl

KAUST Repository

Ahmed, Ejaz; Rothenberger, Alexander

2015-01-01

The new chalcogel CuSb2S4 was obtained by reacting Cu(OAc)2·H2O with KSbS2 in a water/formamide mixture at room temperature. In order to modify the gas adsorption capacity the synthesized CuSb2S4 aerogel was loaded with different amounts of LiCl. CO

Preparation and properties of KCl-doped Cu2O thin film by electrodeposition

International Nuclear Information System (INIS)

Yu, Xiaojiao; Li, Xinming; Zheng, Gang; Wei, Yuchen; Zhang, Ama; Yao, Binghua

2013-01-01

With the indium tin oxide-coated glass as working electrode, cuprous oxide thin film is fabricated by means of electrodeposition. The effects of KCl doped and annealing treatment upon Cu 2 O thin film morphology, surface resistivity, open-circuit voltage, electric conduction types and visible light response are studied. The research results indicate that KCl doped has a great effect upon Cu 2 O crystal morphology, thus, making Cu 2 O thin film surface resistivity drop, and the open-circuit voltage increase and that electric conduction types are transformed from p type into n type, and the visible light (400–500 nm) absorption rate is slightly reduced. Annealing treatment can obviously decrease Cu 2 O thin film surface resistivity and improve its open-circuit voltage. When KCl concentration in electrolytic solution reaches 7 mmol/L, Cu 2 O thin film morphology can be changed from the dendritic crystal into the cubic crystal and Cu 2 O thin film surface resistivity decreases from the initial 2.5 × 10 6 Ω cm to 8.5 × 10 4 Ω cm. After annealing treatment at 320 °C for 30 min, the surface resistivity decreases to 8.5 × 10 2 Ω cm, and the open-circuit voltage increases from the initial 3.1 mV to 79.2 mV.

Integrated Data Collection Analysis (IDCA) Program - KClO₃/Dodecane Mixture

Energy Technology Data Exchange (ETDEWEB)

Sandstrom, Mary M. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Brown, Geoffrey W. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Preston, Daniel N. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Pollard, Colin J. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Warner, Kirstin F. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States). Indian Head Division; Sorenson, Daniel N. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States). Indian Head Division; Remmers, Daniel L. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States). Indian Head Division; Shelley, Timothy J. [Air Force Research Lab. (AFRL), Tyndall AFB, FL (United States); Whinnery, LeRoy L. [Sandia National Lab. (SNL-CA), Livermore, CA (United States); Hsu, Peter C. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Reynolds, John G. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2011-05-23

The Integrated Data Collection Analysis (IDCA) program is conducting a proficiency study for Small-Scale Safety and Thermal (SSST) testing of homemade explosives (HMEs). Described here are the results for impact, friction, electrostatic discharge, and differential scanning calorimetry analysis of a mixture of KClO₃ and dodecane—KClO₃/dodecane mixture. This material was selected because of the challenge of performing SSST testing of a mixture of solid and liquid materials. The mixture was found to: 1) be more sensitive to impact than RDX, and PETN, 2) less sensitive to friction than PETN, and 3) less sensitive to spark than RDX. The thermal analysis showed little or no exothermic features suggesting that the dodecane volatilized at low temperatures. A prominent endothermic feature was observed assigned to melting of KClO₃. This effort, funded by the Department of Homeland Security (DHS), ultimately will put the issues of safe handling of these materials in perspective with standard military explosives. The study is adding SSST testing results for a broad suite of different HMEs to the literature. Ultimately the study has the potential to suggest new guidelines and methods and possibly establish the SSST testing accuracies needed to develop safe handling practices for HMEs. Each participating testing laboratory uses identical test materials and preparation methods wherever possible. Note, however, the test procedures differ among the laboratories. The results are compared among the laboratories and then compared to historical data from various sources. The testing performers involved for the KClO₃/dodecane mixture are Lawrence Livermore National Laboratory (LLNL), Los Alamos National Laboratory (LANL), and Indian Head Division, Naval Surface Warfare Center, (NSWC IHD). These tests are conducted as a proficiency study in order to establish some consistency in test protocols, procedures, and experiments and to understand

Integrated Data Collection Analysis (IDCA) program--KClO₄/Dodecane Mixture

Energy Technology Data Exchange (ETDEWEB)

Sandstrom, Mary M. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Brown, Geoffrey W. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Preston, Daniel N. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Pollard, Colin J. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Warner, Kirstin F. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States). Indian Head Division; Sorensen, Daniel N. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States). Indian Head Division; Remmers, Daniel L. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States). Indian Head Division; Shelley, Timothy J. [Air Force Research Lab. (AFRL), Tyndall AFB, FL (United States); Reyes, Jose A. [Applied Research Associates, Tyndall AFB, FL (United States); Hsu, Peter C. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Reynolds, John G. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2012-05-11

The Integrated Data Collection Analysis (IDCA) program is conducting a proficiency study for Small- Scale Safety and Thermal (SSST) testing of homemade explosives (HMEs). Described here are the results for impact, friction, electrostatic discharge, and differential scanning calorimetry analysis of a mixture of KClO₄ and dodecane—KClO₄/dodecane mixture. This material was selected because of the challenge of performing SSST testing of a mixture of solid and liquid materials. The mixture was found to: 1) be less sensitive to impact than RDX, and PETN, 2) less sensitive to friction than RDX and PETN, and 3) less sensitive to spark than RDX and PETN. The thermal analysis showed little or no exothermic features suggesting that the dodecane volatilized at low temperatures. A prominent endothermic feature was observed and assigned to a phase transition of KClO₄. This effort, funded by the Department of Homeland Security (DHS), ultimately will put the issues of safe handling of these materials in perspective with standard military explosives. The study is adding SSST testing results for a broad suite of different HMEs to the literature. Ultimately the study has the potential to suggest new guidelines and methods and possibly establish the SSST testing accuracies needed to develop safe handling practices for HMEs. Each participating testing laboratory uses identical test materials and preparation methods wherever possible. Note, however, the test procedures differ among the laboratories. The results are compared among the laboratories and then compared to historical data from various sources. The testing performers involved for the KClO₄/dodecane mixture are Lawrence Livermore National Laboratory (LLNL), Los Alamos National Laboratory (LANL), Indian Head Division, Naval Surface Warfare Center, (NSWC IHD), and Air Force Research Laboratory (AFRL/RXQL). These tests are conducted as a proficiency study in order to establish some

X-ray and optical study on point defect formation and interaction under irradiation adn doping of KCl

Energy Technology Data Exchange (ETDEWEB)

Braude, I S; Rogozyanskaya, L M [AN Ukrainskoj SSR, Kharkov. Fiziko-Tekhnicheskij Inst. Nizkikh Temperatur

1978-08-01

Optical and X-ray diffuse scattering methods have been applied to investigate structural changes, taking place in KCl crystals during irradiation with ..gamma..-quanta and doping with barium. It is shown that ..gamma..-irradiation of ''pure'' and doped KCl crystals mainly leads to formation of F-centers and spherical vacancy complexes. F-center concentration in irradiated addition crystals (3x10/sup -6/) has turned out to be 25% lower, than in irradiated pure ones (4x10/sup -6/), which is connected with interaction of radiation and addition defects. The type of defects, causing assymetry in the distribution of diffuse scattering has been determined. Appearance of scattering ability modulation over direction < 100 > during irradiation of KCl pure crystals has been found. Critical radius of spherical complexes formed during irradiation has been estimated, it appeared to be 2.5 a, where a is a lattice period.

Extracellular KCl effect on organic bound tritium in human cells

International Nuclear Information System (INIS)

Gonen, Rafi; Uzi, German; Priel, Esther; Alfassi, Zeev B.

2008-01-01

Tritium atoms can replace hydrogen atoms in organic compounds, forming Organic Bound Tritium. Therefore, exposure of the body to tritium may lead to binding of tritium in tissue molecules, retaining it in the body longer than HTO, and causing higher doses. Ignoring this effect when evaluating inner exposures, may lead to under-estimation of tritium exposures. It was published, that tritium bound to some organic molecules has the potential to accumulate in organisms at higher levels as in the surrounding media. In order to investigate this effect and to identify physiological factors, OBT production in human malignant MG-63 osteoblast cells was studied. The purpose of the present work was to investigate the influence of the ionic extracellular potassium concentration on the amount of tritium in cells. Potassium is known as an ionic compound present in the body, which has the potential to cause cells swelling. Therefore, cells were exposed to isotonic and hypotonic media, supplemented with different concentrations of KCl, and the tritium accumulations were determined after incubation with HTO. An increase in the total Organic Bound Tritium production was observed, as well as an increase of the intracellular HTO content when increasing the KCl concentration. (author)

Molecular Dynamics Simulations on Evaporation of Droplets with Dissolved Salts

OpenAIRE

Jin-Liang Xu; Min Chen; Xiao-Dong Wang; Bing-Bing Wang

2013-01-01

Molecular dynamics simulations are used to study the evaporation of water droplets containing either dissolved LiCl, NaCl or KCl salt in a gaseous surrounding (nitrogen) with a constant high temperature of 600 K. The initial droplet has 298 K temperature and contains 1,120 water molecules, 0, 40, 80 or 120 salt molecules. The effects of the salt type and concentration on the evaporation rate are examined. Three stages with different evaporation rates are observed for all cases. In the initial...

Raman spectroscopic study of the oxidation state of Eu in molten LiCl-KCl

Energy Technology Data Exchange (ETDEWEB)

Park, Seung; Yun, Jong-Il [KAIST, Daejeon(Korea, Republic of)

2016-10-15

Spectroscopy can provide high reliability for the quantitative analysis of such system. The molar absorptivity of Eu(II) at 325 nm is reported as about 1645 M{sup -1}cm{sup -1}, which is too high to apply to higher concentration. A high-temperature Raman spectroscopy has been set and employed for analyzing the molecular structure and coordination complex and investigating the oxidation state of europium in molten LiCl-KCl. Europium can be present in divalent state while many other lanthanides exist in trivalent state. The thermodynamic properties of europium ions have been studied using electrochemical methods, spectroscopic methods, and EPR technique. Although there has been discrepancy of the reduced amount of europium in previous works, the majority of Eu(III) is thought to be reduced to Eu(II) in molten LiCl-KCl spontaneously at relatively low concentration (< 7.5 × 10{sup -4} M). Raman spectroscopy was employed to investigate the oxidation state of EuClx in LiCl-KCl at 500 .deg. C. The Raman scattering results suggest the majority of trivalent europium is reduced to divalent state with the composition change by vaporization. The Raman bands show highly asymmetric structure, quite different from regular octahedral structure.

Thermal Properties of LiCl-KCl Molten Salt for Nuclear Waste Separation

Energy Technology Data Exchange (ETDEWEB)

Sridharan, Kumar [Univ. of Wisconsin, Madison, WI (United States); Allen, Todd [Univ. of Wisconsin, Madison, WI (United States); Anderson, Mark [Univ. of Wisconsin, Madison, WI (United States); Simpson, Mike [Idaho National Lab., (United States)

2012-11-30

This project addresses both practical and fundamental scientific issues of direct relevance to operational challenges of the molten LiCl-KCl salt pyrochemical process, while providing avenues for improvements in the process. In order to understand the effects of the continually changing composition of the molten salt bath during the process, the project team will systematically vary the concentrations of rare earth surrogate elements, lanthanum, cerium, praseodymium, and neodymium, which will be added to the molten LiCl-KCl salt. They will also perform a limited number of focused experiments by the dissolution of depleted uranium. All experiments will be performed at 500 deg C. The project consists of the following tasks. Researchers will measure density of the molten salts using an instrument specifically designed for this purpose, and will determine the melting points with a differential scanning calorimeter. Knowledge of these properties is essential for salt mass accounting and taking the necessary steps to prevent melt freezing. The team will use cyclic voltammetry studies to determine redox potentials of the rare earth cations, as well as their diffusion coefficients and activities in the molten LiCl-KCl salt. In addition, the team will perform anodic stripping voltammetry to determine the concentration of the rare earth elements and their solubilities, and to develop the scientific basis for an on-line diagnostic system for in situ monitoring of the cation species concentration (rare earths in this case). Solubility and activity of the cation species are critically important for the prediction of the salt's useful lifetime and disposal.

Thermal Properties of LiCl-KCl Molten Salt for Nuclear Waste Separation

International Nuclear Information System (INIS)

Sridharan, Kumar; Allen, Todd; Anderson, Mark; Simpson, Mike

2012-01-01

This project addresses both practical and fundamental scientific issues of direct relevance to operational challenges of the molten LiCl-KCl salt pyrochemical process, while providing avenues for improvements in the process. In order to understand the effects of the continually changing composition of the molten salt bath during the process, the project team will systematically vary the concentrations of rare earth surrogate elements, lanthanum, cerium, praseodymium, and neodymium, which will be added to the molten LiCl-KCl salt. They will also perform a limited number of focused experiments by the dissolution of depleted uranium. All experiments will be performed at 500 deg C. The project consists of the following tasks. Researchers will measure density of the molten salts using an instrument specifically designed for this purpose, and will determine the melting points with a differential scanning calorimeter. Knowledge of these properties is essential for salt mass accounting and taking the necessary steps to prevent melt freezing. The team will use cyclic voltammetry studies to determine redox potentials of the rare earth cations, as well as their diffusion coefficients and activities in the molten LiCl-KCl salt. In addition, the team will perform anodic stripping voltammetry to determine the concentration of the rare earth elements and their solubilities, and to develop the scientific basis for an on-line diagnostic system for in situ monitoring of the cation species concentration (rare earths in this case). Solubility and activity of the cation species are critically important for the prediction of the salt's useful lifetime and disposal

Heteroepitaxial strain in alkali halide thin films: KCl on NaCl

DEFF Research Database (Denmark)

Baker, J.; Lindgård, Per-Anker

1999-01-01

We have pet-formed Monte Carlo simulations of the properties of a NaCl (001) surface covered by full or partial layers of KCl, for coverages up to 5 monolayers (ML). A wide variety of structures of the film is found. For integer ML coverages we find the continuous, so-called floating mode rumple ...

Elaboration and characterization of a KCl single crystal doped with nanocrystals of a Sb2O3 semiconductor

International Nuclear Information System (INIS)

Bouhdjer, L.; Addala, S.; Halimi, O.; Boudine, B.; Sebais, M.; Chala, A.

2013-01-01

Undoped and doped KCl single crystals have been successfully elaborated via the Czochralski (Cz) method. The effects of dopant Sb 2 O 3 nanocrystals on structural and optical properties were investigated by a number of techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDAX) analysis, UV-visible and photoluminescence (PL) spectrophotometers. An XRD pattern of KCl:Sb 2 O 3 reveals that the Sb 2 O 3 nanocrystals are in the well-crystalline orthorhombic phase. The broadening of diffraction peaks indicated the presence of a Sb 2 O 3 semiconductor in the nanometer size regime. The shift of absorption and PL peaks is observed near 334 nm and 360 nm respectively due to the quantum confinement effect in Sb 2 O 3 nanocrystals. Particle sizes calculated from XRD studies agree fairly well with those estimated from optical studies. An SEM image of the surface KCl:Sb 2 O 3 single crystal shows large quasi-spherical of Sb 2 O 3 crystallites scattered on the surface. The elemental analysis from EDAX demonstrates that the KCl:Sb 2 O 3 single crystal is slightly rich in oxygen and a source of excessive quantities of oxygen is discussed. (semiconductor materials)

Extraction of actinides from chloride medium using pentaalkylpropanediamides

International Nuclear Information System (INIS)

Cuillerdier, C.; Musikas, C.

1991-01-01

Pyrometallurgical processes for the purification of plutonium create waste solutions containing actinides, mainly americium, in chloride medium. Studies have been undertaken to study the extraction of actinides in chloride medium (hydrochloric acid mixed with concentrated salts such as LiCl, CaCl 2 , MgCl 2 , KCl) using pentaalkylpropanediamides as extractants. Plutonium (IV) is very easily extracted, Am (III) needs a salting out agent such as LiCl. Back extraction of trivalent cations is easy in HCl <5M. Plutonium(IV) and (VI) can be stripped by reduction either with ascorbic acid or hydroxylammonium salts in weak acid medium. Several diluents can be used (aromatic, chlorinated or even aliphatic) with addition of decanol to prevent third phase formation. In conclusion diamides can be used for various wastes declassification, they are potentially completely incinerable, and, as the synthesis has been optimized, they appear to be promising extractants

Specific heat measurements in KCN:KCL mixed crystals

International Nuclear Information System (INIS)

Ghivelder, L.

1983-01-01

An adiabatic calorimeter to perform specific heat measurements of small samples (approximatelly 150 mg) was built. The measurements were taken from 6 to 120 K, iN KCN:KCL mixed crystals, in order to observe the evolution of the antiferroelectric phase transition - that occurs at 83 K in KCN pure. From the experimental results the values of the phase transition critical temperature are found, for some particular concentrations of the mixture, and it was detected that this phase transition disappears with only 10% of Cl - . This result is explained in terms of a change of the potential wells in the crystal. (Author) [pt

Preparation and properties of KCl-doped Cu{sub 2}O thin film by electrodeposition

Energy Technology Data Exchange (ETDEWEB)

Yu, Xiaojiao, E-mail: yxjw@xaut.edu.cn [Xi’an University of Technology, Xi’an 710048 (China); Li, Xinming [Xi’an University of Technology, Xi’an 710048 (China); Zheng, Gang [Xi’an University of Technology, Xi’an 710048 (China); Northwestern Polytechnical University, Xi’an 710072 (China); Wei, Yuchen [The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong (China); Zhang, Ama; Yao, Binghua [Xi’an University of Technology, Xi’an 710048 (China)

2013-04-01

With the indium tin oxide-coated glass as working electrode, cuprous oxide thin film is fabricated by means of electrodeposition. The effects of KCl doped and annealing treatment upon Cu{sub 2}O thin film morphology, surface resistivity, open-circuit voltage, electric conduction types and visible light response are studied. The research results indicate that KCl doped has a great effect upon Cu{sub 2}O crystal morphology, thus, making Cu{sub 2}O thin film surface resistivity drop, and the open-circuit voltage increase and that electric conduction types are transformed from p type into n type, and the visible light (400–500 nm) absorption rate is slightly reduced. Annealing treatment can obviously decrease Cu{sub 2}O thin film surface resistivity and improve its open-circuit voltage. When KCl concentration in electrolytic solution reaches 7 mmol/L, Cu{sub 2}O thin film morphology can be changed from the dendritic crystal into the cubic crystal and Cu{sub 2}O thin film surface resistivity decreases from the initial 2.5 × 10{sup 6} Ω cm to 8.5 × 10{sup 4} Ω cm. After annealing treatment at 320 °C for 30 min, the surface resistivity decreases to 8.5 × 10{sup 2} Ω cm, and the open-circuit voltage increases from the initial 3.1 mV to 79.2 mV.

Method for treating electrolyte to remove Li.sub.2 O

Science.gov (United States)

Tomczuk, Zygmunt; Miller, William E.; Johnson, Gerald K.; Willit, James L.

1998-01-01

A method of removing Li.sub.2 O present in an electrolyte predominantly of LiCl and KCl. The electrolyte is heated to a temperature not less than about 500.degree. C. and then Al is introduced into the electrolyte in an amount in excess of the stoichiometric amount needed to convert the Li.sub.2 O to a Li-Al alloy and lithium aluminate salt. The salt and aluminum are maintained in contact with agitation for a time sufficient to convert the Li.sub.2 O.

Physicochemical properties of low sodium frankfurter with added walnut: effect of transglutaminase combined with caseinate, KCl and dietary fibre as salt replacers.

Science.gov (United States)

Colmenero, F Jiménez; Ayo, M J; Carballo, J

2005-04-01

This study compares the effects of combinations of microbial transglutaminase (TGase) and various non-meat ingredients (caseinate, KCl and wheat fibre) used as salt replacers, with the effects of NaCl on the physicochemical properties (cooking loss, emulsion stability, texture and colour) of frankfurters with added walnuts. The combination of TGase with caseinate, KCl or fibre led to harder, springier and chewier (Pcaseinate>KCl>fibre. Frankfurters with caseinate presented the highest lightness and the lowest redness values. Frankfurter with NaCl had a harder, springier and chewier gel/emulsion network with lower cooking loss than those NaCl free.

Galvanic reduction of uranium(III) chloride from LiCl-KCl eutectic salt using gadolinium metal

Science.gov (United States)

Bagri, Prashant; Zhang, Chao; Simpson, Michael F.

2017-09-01

The drawdown of actinides is an important unit operation to enable the recycling of electrorefiner salt and minimization of waste. A new method for the drawdown of actinide chlorides from LiCl-KCl molten salt has been demonstrated here. Using the galvanic interaction between the Gd/Gd(III) and U/U(III) redox reactions, it is shown that UCl3 concentration in eutectic LiCl-KCl can be reduced from 8.06 wt.% (1.39 mol %) to 0.72 wt.% (0.12 mol %) in about an hour via plating U metal onto a steel basket. This is a simple process for returning actinides to the electrorefiner and minimizing their loss to the salt waste stream.

Separation of CsCl and SrCl_2 from a ternary CsCl-SrCl_2-LiCl via a zone refining process for waste salt minimization of pyroprocessing

International Nuclear Information System (INIS)

Shim, Moonsoo; Choi, Ho Gil; Yi, Kyung Woo; Hwang, Il Soon; Lee, Jong Hyeon

2016-01-01

The purification of LiCl salt mixture has traditionally been carried out by a melt crystallization process. To improve the throughput of zone refining, three heaters were installed in the zone refiner. The zone refining method was used to grow pure LiCl salt ingots from LiCl-CsCl-SrCl_2 salt mixture. The main investigated parameters were the heater speed and the number of passes. A change in the LiCl crystal grain size was observed according to the horizontal direction. From each zone refined salt ingot, samples were collected horizontally. To analyze the concentrations of Sr and Cs, an inductively coupled plasma optical emission spectrometer and inductively coupled plasma mass spectrometer were used, respectively. The experimental results show that Sr and Cs concentrations at the initial region of the ingot were low and reached their peak at the final freezing region of the salt ingot. Concentration results of zone refined salt were compared with theoretical results yielded by the proposed model to validate its predictions. The k_e_f_f of Sr and Cs were 0.13 and 0.11, respectively. The decontamination factors of Sr and Cs were 450 and 1650, respectively. - Highlights: • The LiCl-CsCl-SrCl_2 salt ingot was purified by zone refining technique to minimize waste salt. • The concentration distribution of Cs and Sr were analyzed by mass transfer equation. • The decontamination factors of Cs and Sr were 1600 and 450 respectively in case of 60% of recovery yield.

Pressure induced structural phase transition in solid oxidizer KClO3: A first-principles study

Science.gov (United States)

Yedukondalu, N.; Ghule, Vikas D.; Vaitheeswaran, G.

2013-05-01

High pressure behavior of potassium chlorate (KClO3) has been investigated from 0 to 10 GPa by means of first principles density functional theory calculations. The calculated ground state parameters, transition pressure, and phonon frequencies using semiempirical dispersion correction scheme are in excellent agreement with experiment. It is found that KClO3 undergoes a pressure induced first order phase transition with an associated volume collapse of 6.4% from monoclinic (P21/m) → rhombohedral (R3m) structure at 2.26 GPa, which is in good accord with experimental observation. However, the transition pressure was found to underestimate (0.11 GPa) and overestimate (3.57 GPa) using local density approximation and generalized gradient approximation functionals, respectively. Mechanical stability of both the phases is explained from the calculated single crystal elastic constants. In addition, the zone center phonon frequencies have been calculated using density functional perturbation theory at ambient as well as at high pressure and the lattice modes are found to soften under pressure between 0.6 and 1.2 GPa. The present study reveals that the observed structural phase transition leads to changes in the decomposition mechanism of KClO3 which corroborates with the experimental results.

Carrageenan :the difference between PNG and KCL gel precipitation method as Lactobacillus acidophilus encapsulation material

Science.gov (United States)

Setijawati, D.; Nursyam, H.; Salis, H.

2018-04-01

The study on the effects of using of materials and methods in the preparation of the microcapsules Lactobacillus acidophilus towards the viability has been done. The research method used is experimental laboratory design. Variable research was kind of material (A) as the first factor with sub factor (A1 = Eucheuma cottonii) (A2 = Eucheuma spinosum) (A3 = mixture of Eucheuma cottonii and Eucheuma spinosum 1:1 ratio), while the second factor is a method of extraction to produce caragenan (B) with sub factor (B1 = Philipine Natural Grade modification) (B2 = KCl gel Press Precipitation). Analysis of different influences uses Analysis Of Varians followed by Fisher’s test. Analysis of data uses Mini tab 16. The results shows that the kind of extraction factors and methods gave significantly different effects on the viability of Lactobacillus acidophilus. The highest mean of Viablity obtained in the treatment of materials with a mixture of Eucheuma cottonii and Eucheuma spinosum and used KCl Gel Press method is equal to 7.14 log (CFU / mL). It is ssuggested using of kappa-iota carrageenanmixture asencapsulation material with KCl Gel Press method on Lactobacillus acidophilus microencapsulation process because it treatment gavethe highest average of Lactobacillus acidophilus viability.

Electric conductivity of molten mixtures of ternary mutual KF-KCl-ZrF4 system

International Nuclear Information System (INIS)

Darienko, S.E.; Raspopin, S.P.; Chervinskij, Yu.F.

1988-01-01

Using the relative capillary method at the frequency of 50 kHz the specific electric conductivity of molten mixtures of the KF-KCl-ZnF 4 system is measured. All the measurements were made in the atmosphere of purified argon. Temperature dependence of electric conductivity of the mixtures studied (800-1260 K) is described by the equations of exponential type with sufficient accuracy. Curves of identical specific electric conductivity of the three-component system are presented. With an increase in zirconium tetrachloride concentration in the mixtures electric conductivity of the melts decreases. On the basis of the measurement results of KF-ZrF 4 and KCl-ZrF 4 molten mixture specific electric conductivity and data on the melt density the values of molar electric conductivity at 1200 K are calculated

Effect of α1-adrenergic stimulation on phosphoinositide metabolism and protein kinase C (PK-C) in rat cardiomyocytes

International Nuclear Information System (INIS)

Kaku, T.; Lakatta, E.; Filburn, C.R.

1986-01-01

Alpha 1 -adrenergic stimulation is known to enhance membrane phospholipid metabolism resulting in increases in inositol phosphates (IP's) and diacylglycerol (DAG). Cardiomyocytes prelabeled with 3 H-myo-inositol were treated with norepinephrine (NE) for 1-15 min, acid extracted, and IP's separated by ion exchange chromatography. Addition of NE (10 -5 M) in the presence of propranolol (10 -5 M) and LiCl (9 mM) enhanced the accumulation of IP's, linearly with time up to 15 min, and reached 7.3, and 1.5-fold at 15 min for IP 1 , IP 2 , and IP 3 , respectively. KCl at 30 mM had no effect on accumulation of IP's, but augmented the effect of NE. PK-C activity was measured in both cytosol (S) and particulate (P) fractions of treated cells. NE alone had a negligible effect on membrane PK-C, while 30 mM KCl caused a small increase. However, pretreatment with KCl followed by NE produced a significant increase above that seen with KCl alone. Dioctanoylglycerol also stimulated membrane association of PK-C in these cells. These data suggest that α 1 -adrenergic stimulation of membrane association of myocardial PK-C is mediated by DAG but may be dependent on membrane potential and/or the extent of Ca 2+ loading

Application of the rotating cylinder electrode in molten LiCl-KCl eutectic containing uranium(III)- and magnesium(II)-chloride

Energy Technology Data Exchange (ETDEWEB)

Rappleye, Devin, E-mail: rappleye1@llnl.gov; Simpson, Michael F.

2017-04-15

The application of the rotating cylinder electrode (RCE) to molten LiCl-KCl eutectic mixtures for electroanalytical measurements is presented. This enabled the measurement of the limiting current which was observed to follow a linear trend with the rotational rate raised to 0.64–0.65 power on average, which closely agrees with existing RCE mass-transfer correlations. This is the first publication of electroanalytical RCE measurements in LiCl-KCl eutectic based molten salt mixtures, to our knowledge. These measurements were made in mixtures of molten LiCl-KCl eutectic containing UCl{sub 3} and MgCl{sub 2}. Kinetic parameters were calculated for Mg{sup 2+} in LiCl-KCl eutectic. The exchange current density (i{sub o}) of Mg{sup 2+} deposition varied with mole fraction (x) according to i{sub o}(A cm{sup −2}) = 1.64x{sup 0.689}. The parameters from RCE measurements were also applied in an electrochemical co-deposition model entitled DREP to detect and predict the deposition rate of U and Mg. DREP succeeded in detecting the co-deposition of U and Mg, even when Mg constituted less than 0.5 wt% of the deposit.

Characteristics of dechlorination for LiCl salt by the surface temperature-controlled reactor

Energy Technology Data Exchange (ETDEWEB)

Cho, In Hak [Chungnam National University, Daejeon (Korea, Republic of); Park, Hwan Seo; Ahn, Soo Na; Eun, Hee Chul; Kim, In Tae; Cho, Yong Jun [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2011-05-15

Molten salt waste is generated from a pyrochemical process to separate reusable U and TRU elements from a spent nuclear fuel. The spent lithium chloride waste is highly soluble in water and contains volatile radioactive elements such as Cs. However, these wastes are difficult to directly immobilize into durable matrix such as glass or ceramic wasteform for final disposal. ANL(Argonne National Laboratory) suggested the conversion of metal chloride into a sodalite for the immobilization of a chloride waste, glass-bonded sodalite, which was fabricated at about 915 .deg. C after mixing the salt-loaded zeolite and borosilicate glass powder. Although this wasteform shows high leach-resistance, the waste volume greatly increases. The previous study was to treat metal chloride wastes by using SAP(SiO{sub 2}-Al{sub 2}O{sub 3}-P{sub 2}O{sub 5}) materials. By using this method, the final waste volume reduced and leach-resistance was good. In this study, characteristics of dechlorination reaction of LiCl with an inorganic composite, SAP, was investigated by using a specific surface temperature-controlled reactor

Integrated Data Collection Analysis (IDCA) Program — KClO₃ (as received)/Icing Sugar

Energy Technology Data Exchange (ETDEWEB)

Sandstrom, Mary M. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Brown, Geoffrey W. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Preston, Daniel N. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Pollard, Colin J. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Warner, Kirstin F. [Naval Surface Warfare Center (NSWC IHD), Indian Head, MD (United States). Indian Head Division; Sorenson, Daniel N. [Naval Surface Warfare Center (NSWC IHD), Indian Head, MD (United States). Indian Head Division; Remmers, Daniel L. [Naval Surface Warfare Center (NSWC IHD), Indian Head, MD (United States). Indian Head Division; Shelley, Timothy J. [Air Force Research Lab. (AFRL/RXQL), Tyndall AFB, FL (United States); Reyes, Jose A. [Applied Research Associates, Inc., Tyndall AFB, FL (United States); Hsu, Peter C. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Whipple, Richard E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Reynolds, John G. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2011-05-23

The Integrated Data Collection Analysis (IDCA) program is conducting a proficiency study for Small-Scale Safety and Thermal (SSST) testing of homemade explosives (HMEs). Described here are the results for impact, friction, electrostatic discharge, and differential scanning calorimetry analysis of a mixture of KClO₃ as received from the manufacturer mixed with icing sugar, sized through a 100-mesh sieve—KClO₃/icing sugar (AR) mixture. This material was selected because of the challenge of performing SSST testing of a mixture of two solid materials. The mixture was found to: 1) be more sensitive to impact than RDX, similar to PETN, 2) be the same or less sensitive to friction than PETN, and 3) to be less sensitive to spark than RDX. The thermal analysis showed that the mixture has thermally stability similar to RDX and is perhaps more energetic upon decomposition but variable results indicate sampling issues. Compared to the 100-mesh sieved counter part, the KClO₃/icing sugar (-100) mixture, the AR mixture was found to be about the same sensitivity towards impact, friction and ESD.

Direct reduction of uranium oxide(U3O8) by Li metal and U-metal(Fe, Ni) alloy formation in molten LiCl medium

International Nuclear Information System (INIS)

Cho, Young Hwan; Kim, Tack Jin; Choi, In Kyu; Kim, Won Ho; Jee, Kwang Yong

2004-01-01

Molten salt based electrochemical processes are proposed as a promising method for the future nuclear programs and more specifically for spent fuel processing. The lithium reduction has been introduced to convert actinide oxides into corresponding actinide metal by using lithium metal as a reductant in molten LiCl medium. We have applied similar lab-scale experiments to reduce uranium oxide in an effort to gain additional information on rates and mechanisms

Investigation of residual anode material after electrorefining uranium in molten chloride salt

Energy Technology Data Exchange (ETDEWEB)

Rose, M.A., E-mail: marose@anl.gov [Department of Nuclear Engineering, Purdue University, West Lafayette, IN, 47907 (United States); Nuclear Engineering Division, Argonne National Laboratory, Argonne, IL 60439 (United States); Williamson, M.A.; Willit, J. [Nuclear Engineering Division, Argonne National Laboratory, Argonne, IL 60439 (United States)

2015-12-15

A buildup of material at uranium anodes during uranium electrorefining in molten chloride salts has been observed. Potentiodynamic testing has been conducted using a three electrode cell, with a uranium working electrode in both LiCl/KCl eutectic and LiCl each containing ∼5 mol% UCl{sub 3}. The anodic current response was observed at 50° intervals between 450 °C and 650 °C in the eutectic salt. These tests revealed a buildup of material at the anode in LiCl/KCl salt, which was sampled at room temperature, and analyzed using ICP-MS, XRD and SEM techniques. Examination of the analytical data, current response curves and published phase diagrams has established that as the uranium anode dissolves, the U{sup 3+} ion concentration in the diffusion layer surrounding the electrode rises precipitously to levels, which may at low temperatures exceed the solubility limit for UCl{sub 3} or in the case of the eutectic salt for K{sub 2}UCl{sub 5}. The reduction in current response observed at low temperature in eutectic salt is eliminated at 650 °C, where K{sub 2}UCl{sub 5} is absent due to its congruent melting and only simple concentration polarization effects are seen. In LiCl similar concentration effects are seen though significantly longer time at applied potential is required to effect a reduction in the current response as compared to the eutectic salt.

Effect of oxygen on the complexing and electrochemical processes in the NaCl-KCl-K2TaF7 melt

International Nuclear Information System (INIS)

Polyakova, L.P.; Kononova, Z.A.; Kremenetskij, V.G.; Polyakov, E.K.

1997-01-01

Using the method of linear voltametry oxygen influence on electrochemical behaviour of tantalum during NaCl-KCl-K 2 TaF 7 melt titration with sodium oxide is studied. It is shown that in NaCl-KCl-K 3 TaOF 6 and NaCl-KCl-K 2 TaF 7 -Na 2 O melts (at molar ratio O/Ta = 1 ) tantalum reduction proceeds from oxyhalide complex of TaOClF 5 -3 composition. On further titration with sodium oxide (1 5 3- complexes, but their concentration is decreased at the cost of formation of insoluble compound K 0,4 TaO 2,4 F 0,6 . When O/Ta ≥ 2,4 tantalum concentration in electrolyte is decreased up to zero and peak of tantalum reduction on voltamogram is not recorded. (author)

Electrochemical study of uranium cations in LiCl-KCl melt using a rotating disk electrode

Energy Technology Data Exchange (ETDEWEB)

Bae, Sang-Eun; Kim, Dae-Hyun; Kim, Jong-Yoon; Park, Tae-Hong; Cho, Young Hwan; Yeon, Jei-Won; Song, Kyuseok [Nuclear Chemistry Research Division, Korea Atomic Energy Research Institute,989-111 Daedeok-daero, Yuseong-gu, Daejeon, 305-353 (Korea, Republic of)

2013-07-01

A rotating disk electrode (RDE) measurement technique was employed to investigate the electrochemical REDOX reactions of actinide (An) and lanthanide (Ln) ions in LiCl-KCl molten salt. By using RDE, it is possible to access more exact values of the diffusion coefficient, Tafel slope, and exchange current density. In this work, we constructed RDE setup and electrodes for RDE measurements in high temperature molten salt and measured the electrochemical parameters of the An and Ln ions. The RDE setup is composed of a Pine model MSRX rotator equipped with a rod type of W electrode. The active electrode area was confined to the planar part of the W rod by making meniscus at the LiCl-KCl melt surface.

Hot electrons and the approach to metallic behavior in Kx(KCl)1-x

NARCIS (Netherlands)

Silvestrelli, P.L.; Alavi, A.; Parrinello, M.; Frenkel, D.

1996-01-01

The approach to the metallic phase of molten Kx(KCl)1-x mixtures is studied using ab initio molecular dynamics based on finite-temperature density functional theory. The finite electronic temperature is found to result in new and unexpected effects. In particular, we observe a thermally induced

Pyro-Electrochemical Reduction of a Mixture of Rare Earth Oxides and NiO in LiCl molten Salt

Energy Technology Data Exchange (ETDEWEB)

Lee, Min Woo; Jeong, Sang Mun [Department of Chemical Engineering, Chungbuk National University, Cheongju (Korea, Republic of)

2017-06-15

An electrochemical reduction of a mixture of NiO and rare earth oxides has been conducted to increase the reduction degree of rare earth oxides. Cyclic voltammetry (CV) measurement was carried out to determine the electrochemical reduction behavior of the mixed oxide in molten LiCl medium. Constant voltage electrolysis was performed with various supplied charges to understand the mechanism of electrochemical reduction of the mixed oxide as a working electrode. After completion of the electrochemical reduction, crystal structure of the reaction intermediates was characterized by using an X-ray diffraction method. The results clearly demonstrate that the rare earth oxide was converted to RE-Ni intermetallics via co-reduction with NiO.

Recovery of Residual LiCl-KCl Eutectic Salts in Radioactive Rare Earth Precipitates

International Nuclear Information System (INIS)

Eun, Hee Chul; Yang, Hee Chul; Kim, In Tae; Lee, Han Soo; Cho, Yung Zun

2010-01-01

For the pyrochemical process of spent nuclear fuels, recovery of LiCl-KCl eutectic salts is needed to reduce radioactive waste volume and to recycle resource materials. This paper is about recovery of residual LiCl-KCl eutectic salts in radioactive rare earth precipitates (rare earth oxychlorides or oxides) by using a vacuum distillation process. In the vacuum distillation test apparatus, the salts in the rare earth precipitates were vaporized and were separated effectively. The separated salts were deposited in three positions of the vacuum distillation test apparatus or were collected in the filter and it is difficult to recover them. To resolve the problem, a vacuum distillation and condensation system, which is subjected to the force of a temperature gradient at a reduced pressure, was developed. In a preliminary test of the vacuum distillation/condensation recovery system, it was confirmed that it was possible to condense the vaporized salts only in the salt collector and to recover the condensed salts from the salt collector easily

"INHIBITORY EFFECT OF ALUMINIUM ON KCL AND PHENYLEPHRINE INDUCED CONTRACTION IN ISOLATED RAT AORTA"

Directory of Open Access Journals (Sweden)

T. Mashhoodi

2004-10-01

Full Text Available It has been shown in some investigations that cardiovascular events are the main causes of death in hemodialysis patients. The exact etiology is unknown but some of the articles have reported a relation between aluminium ions in the dialysis solution and cardiovascular disorders. To determine the probable effect of aluminium on vasculature function, in vitro effects of aluminium ion on vasoconstriction induced by KCl (30 mM or phenylephrine (10 µM were investigated using isolated rat aorta. AlCl3 (1-4 mM decreased both KCl and phenylephrine induced contractions in a dose dependent manner (P<0.01. Complete inhibition of the contractions occurred using the higher doses of aluminium. Results of this study suggest that because of inhibitory effects of aluminium on vascular contractions, the probable cardiovascular dysfunction must be considered in aluminium intoxication.

Radiolysis of concentrated solutions. 1. Pulse and γ radiolysis studies of direct and indirect effects in LiCl solutions

International Nuclear Information System (INIS)

Pucheault, J.; Ferradini, C.; Julien, R.; Deysine, A.; Gilles, L.; Moreau, M.

1979-01-01

This study of the radiolysis of concentrated aqueous LiCl solutions enables the relative contributions of the direct and indirect effects to be evaluated as a function of Cl - concentration and also permits an evaluation of the role of Cl - in the early stages of water radiolysis. Radicalar and molecular yields G/sub Cl 2 - /, G/sub OH/, G//sub e//sub aq/ - / + G/sub H/, G/sub H 2 O 2 /, and G/sub H 2 / are determined for all concentrations employed, and the material balance is verified. The main conclusions concerning the apparent inefficacy of the direct effect and the importance of OH scavenging in spurs are discussed

Enhancement in CO2 Adsorption Capacity and Selectivity in the Chalcogenide Aerogel CuSb2S4 by Post-synthetic Modification with LiCl

KAUST Repository

Ahmed, Ejaz

2015-09-11

The new chalcogel CuSb2S4 was obtained by reacting Cu(OAc)2·H2O with KSbS2 in a water/formamide mixture at room temperature. In order to modify the gas adsorption capacity the synthesized CuSb2S4 aerogel was loaded with different amounts of LiCl. CO2 adsorption measurements on the CuSb2S4 aerogel before and after treatment with LiCl showed more than three times increased uptake of the LiCl-modified chalcogel. The selectivities of the gas pairs CO2/H2 and CO2/CH4 in the LiCl-treated chalcogel are 235 and 105 respectively and amongst the highest reported for chalcogenide-based aerogels. In comparison with other porous materials like zeolites, activated carbon and most of the Metal Organic Frameworks (MOFs) or Porous Organic Frameworks (POFs), our synthesized aerogels show good air and moisture stability. Although, the CO2 storage capacity of our aerogels is relatively low, however the selectivity of CO2 over H2 or CH4 in LiCl-loaded aerogels are higher than in zeolites, activated carbon as well as some MOFs like Cu-BTC and MOF-5 etc.

Fuel-coolant interactions in a shock-tube geometry

International Nuclear Information System (INIS)

Segev, A.; Henry, R.E.; Bankoff, S.G.

1978-01-01

Thermal interactions were studied in a shock tube configuration using different pairs of liquids. Large pressures were obtained for systems of water-Wood's metal and butanol-Wood's metal. Different types of interactions were observed, depending on the hot liquid temperature. It was found that thehydrodynamic component alone may account for the measured pressure in the lower temperature range. A combination of thermal and hydrodynamic interactions accounts for the pressures at high temperatures. Experiments with water and molten salt (LiCl + KCl) produced small scale explosions. All interactions were suppressed when driving pressure increased. (author)

Method for treating electrolyte to remove Li{sub 2}O

Science.gov (United States)

Tomczuk, Z.; Miller, W.E.; Johnson, G.K.; Willit, J.L.

1998-01-20

A method is described for removing Li{sub 2}O present in an electrolyte predominantly of LiCl and KCl. The electrolyte is heated to a temperature not less than about 500 C and then Al is introduced into the electrolyte in an amount in excess of the stoichiometric amount needed to convert the Li{sub 2}O to a Li-Al alloy and lithium aluminate salt. The salt and aluminum are maintained in contact with agitation for a time sufficient to convert the Li{sub 2}O.

Saturated vapor pressure over molten mixtures of GaCl3 and alkali metal chlorides

International Nuclear Information System (INIS)

Salyulev, A.B.; Smolenskij, V.V.; Moskalenko, N.I.

2004-01-01

Volatilities of GaCl 3 and alkali metal chlorides over diluted (up to 3 mol %) solutions of GaCl 3 in LiCl, NaCl, KCl, RbCl, and CsCl were measured at 1100 K by dynamic and indirect static methods. Chemical composition of saturated vapor over the mixed melts was determined. Partial pressures of the components were calculated. Their values depend essentially on specific alkali metal cation and on concentration of GaCl 3 ; their variation permits altering parameters of GaCl 3 distillation from the salt melt in a wide range [ru

A density model based on the Modified Quasichemical Model and applied to the (NaCl + KCl + ZnCl2) liquid

International Nuclear Information System (INIS)

Ouzilleau, Philippe; Robelin, Christian; Chartrand, Patrice

2012-01-01

Highlights: ► A model for the density of multicomponent inorganic liquids. ► The density model is based on the Modified Quasichemical Model. ► Application to the (NaCl + KCl + ZnCl 2 ) ternary liquid. ► A Kohler–Toop-like asymmetric interpolation method was used. - Abstract: A theoretical model for the density of multicomponent inorganic liquids based on the Modified Quasichemical Model has been presented previously. By introducing in the Gibbs free energy of the liquid phase temperature-dependent molar volume expressions for the pure components and pressure-dependent excess parameters for the binary (and sometimes higher-order) interactions, it is possible to reproduce, and eventually predict, the molar volume and the density of the multicomponent liquid phase using standard interpolation methods. In the present article, this density model is applied to the (NaCl + KCl + ZnCl 2 ) ternary liquid and a Kohler–Toop-like asymmetric interpolation method is used. All available density data for the (NaCl + KCl + ZnCl 2 ) liquid were collected and critically evaluated, and optimized pressure-dependent model parameters have been found. This new volumetric model can be used with Gibbs free energy minimization software, to calculate the molar volume and the density of (NaCl + KCl + ZnCl 2 ) ternary melts.

Integrated Data Collection Analysis (IDCA) Program - KClO₄/Carbon Mixture

Energy Technology Data Exchange (ETDEWEB)

Sandstrom, Mary M. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Brown, Geoffrey W. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Preston, Daniel N. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Pollard, Colin J. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Warner, Kirstin F. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States). Indian Head Division; Sorensen, Daniel N. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States). Indian Head Division; Remmers, Daniel L. [Naval Surface Warfare Center (NSWC), Indian Head, MD (United States). Indian Head Division; Shelley, Timothy J. [Air Force Research Lab. (AFRL), Tyndall AFB, FL (United States); Reyes, Jose A. [Applied Research Associates, Tyndall AFB, FL (United States); Hsu, Peter C. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Reynolds, John G. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2013-01-31

The Integrated Data Collection Analysis (IDCA) program is conducting a proficiency study for Small- Scale Safety and Thermal (SSST) testing of homemade explosives (HMEs). Described here are the results for impact, friction, electrostatic discharge, and differential scanning calorimetry analysis of a mixture of KClO₄ and activated carbon—KClO₄/C mixture. This material was selected because of the challenge of performing SSST testing of a mixture of two solids. The mixture was found to be insensitive to impact, friction, and thermal stimulus, and somewhat sensitive to spark discharge. This effort, funded by the Department of Homeland Security (DHS), ultimately will put the issues of safe handling of these materials in perspective with standard military explosives. The study is adding SSST testing results for a broad suite of different HMEs to the literature. Ultimately the study has the potential to suggest new guidelines and methods and possibly establish the SSST testing accuracies needed to develop safe handling practices for HMEs. Each participating testing laboratory uses identical test materials and preparation methods wherever possible. Note, however, the test procedures differ among the laboratories. The results are compared among the laboratories and then compared to historical data from various sources. The testing performers involved for the KClO₄/carbon mixture are Lawrence Livermore National Laboratory (LLNL), Los Alamos National Laboratory (LANL), Indian Head Division, Naval Surface Warfare Center, (NSWC IHD), and Air Force Research Laboratory (AFRL/RXQL). These tests are conducted as a proficiency study in order to establish some consistency in test protocols, procedures, and experiments and to understand how to compare results when these testing variables cannot be made consistent.

Protective roles of bacterioruberin and intracellular KCl in the resistance of Halobacterium salinarium against DNA-damaging agents

International Nuclear Information System (INIS)

Shahmohammadi, H.R.; Asgarani, E.; Terato, Hiroaki; Saito, Takeshi; Ohyama, Yoshihiko; Gekko, Kunihiko; Yamamoto, Osamu; Ide, Hiroshi

1998-01-01

Halobacterium salinarium, a member of the extremely halophilic archaebacteria, contains a C 50 -carotenoid namely bacterioruberin. We have previously reported the high resistance of this organism against the lethal actions of DNA-damaging agents including ionizing radiation and ultraviolet light (UV). In this study, we have examined whether bacterioruberin and the highly concentrated salts in this bacterium play protective roles against the lethal actions of ionizing radiation, UV, hydrogen peroxide, and mitomycin-C (MMC). The colourless mutant of H. salinarium deficient in bacterioruberin was more sensitive than the red-pigmented wild-type to all tested DNA-damaging agents except MMC. Circular dichroism (CD) spectra of H. salinarium chromosomal DNA at various concentrations of KCl (0-3.5 M) were similar to that of B-DNA, indicating that no conformational changes occurred as a result of high salt concentrations. However, DNA strand-breaks induced by ionizing radiation were significantly reduced by the presence of either bacterioruberin or concentrated KCl, presumably due to scavenging of free radicals. These results suggest that bacterioruberin and intracellular KCl of H. salinarium protect this organism against the lethal effects of oxidative DNA-damaging agents. (author)

Separation of CsCl and SrCl{sub 2} from a ternary CsCl-SrCl{sub 2}-LiCl via a zone refining process for waste salt minimization of pyroprocessing

Energy Technology Data Exchange (ETDEWEB)

Shim, Moonsoo [Graduate School of Energy Science and Technology, Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon, 34134 (Korea, Republic of); Choi, Ho Gil; Yi, Kyung Woo; Hwang, Il Soon [Graduate School of Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826 (Korea, Republic of); Lee, Jong Hyeon, E-mail: jonglee@cnu.ac.kr [Graduate School of Energy Science and Technology, Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon, 34134 (Korea, Republic of); Graduate School of Department of Advanced Materials Engineering, Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon, 34134 (Korea, Republic of); Rapid Solidified Materials Research Center, Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon, 34134 (Korea, Republic of)

2016-11-15

The purification of LiCl salt mixture has traditionally been carried out by a melt crystallization process. To improve the throughput of zone refining, three heaters were installed in the zone refiner. The zone refining method was used to grow pure LiCl salt ingots from LiCl-CsCl-SrCl{sub 2} salt mixture. The main investigated parameters were the heater speed and the number of passes. A change in the LiCl crystal grain size was observed according to the horizontal direction. From each zone refined salt ingot, samples were collected horizontally. To analyze the concentrations of Sr and Cs, an inductively coupled plasma optical emission spectrometer and inductively coupled plasma mass spectrometer were used, respectively. The experimental results show that Sr and Cs concentrations at the initial region of the ingot were low and reached their peak at the final freezing region of the salt ingot. Concentration results of zone refined salt were compared with theoretical results yielded by the proposed model to validate its predictions. The k{sub eff} of Sr and Cs were 0.13 and 0.11, respectively. The decontamination factors of Sr and Cs were 450 and 1650, respectively. - Highlights: • The LiCl-CsCl-SrCl{sub 2} salt ingot was purified by zone refining technique to minimize waste salt. • The concentration distribution of Cs and Sr were analyzed by mass transfer equation. • The decontamination factors of Cs and Sr were 1600 and 450 respectively in case of 60% of recovery yield.

Thermoluminescence of the Z centre in Mg-doped KCl

International Nuclear Information System (INIS)

Kamavisdar, V.S.; Deshmukh, B.T.

1980-01-01

Optical absorption and thermoluminescence measurements on KCl:Mg 2+ are reported. Bleaching in F band introduces a new glow peak at 406 K in the glow curves. A similar peak is observed in microcrystalline powders. When this peak is thermally cleaned, the broadening of the absorption observed in prolonged F bleached crystals is removed. On the basis of these observations, the glow peak at 406 K is tentatively attributed to Z 1 centres. The glow peak at 394 K observed in microcrystalline powders is attributed to a combined effect of deformation and Z 1 centres. (author)

Application of aluminum diffusion coatings to mitigate the KCl-induced high-temperature corrosion

DEFF Research Database (Denmark)

Kiamehr, Saeed; Lomholt, T. N.; Dahl, Kristian Vinter

2017-01-01

Pack cementation was used to produce Fe1−xAl and Fe2Al5 diffusion coatings on ferritic-martensitic steel P91 and a Ni2Al3 diffusion coating on pure nickel. The performance of diffusion coatings against high-temperature corrosion induced by potassium chloride (KCl) was evaluated by exposing...

Simulation of NaCl and KCl mass transfer during salting of Prato cheese in brine with agitation: a numerical solution

Directory of Open Access Journals (Sweden)

E. Bona

2007-09-01

Full Text Available The association of dietary NaCl with arterial hypertension has led to a reduction in the levels of this salt in cheeses. For salting, KCl has been used as a partial substitute for NaCl, which cannot be completely substituted without affecting product acceptability. In this study a sensorially adequate saline solution (NaCl/KCl was simultaneously diffused during salting of Prato cheese in brine with agitation. The simultaneous multicomponent diffusion during the process was modeled with Fick’s second generalized law. The system of partial differential equations formed was solved by the finite element method (FEM. In the experimental data concentration the deviation for NaCl was of 7.3% and for KCl of 5.4%, both of which were considered acceptable. The simulation of salt diffusion will allow control and modulation of salt content in Prato cheese, permitting the prediction of final content from initial conditions.

Electron paramagnetic resonance of K3Rh(CN)6 irradiated with electrons in KCl

International Nuclear Information System (INIS)

Vugman, N.V.

1970-07-01

Using a simple theory, it was estimated the electronic density of the diamagnetic complex Rh (CN) 3- 6 in a KCl lattice. The g// and g1 values were determined by EPR, and the experimental results fit the theoretical calculations. (M.W.O.) [pt

Vacuum evaporation of KCl-NaCl salts. Part 2: Vaporization-rate model and experimental results

International Nuclear Information System (INIS)

Wang, L.L.; Wallace, T.C. Sr.; Hampel, F.G.; Steele, J.H.

1996-01-01

Separation of chloride salts from the actinide residue by vacuum evaporation is a promising method of treating wastes from the pyrochemical plutonium processes. A model based on the Hertz-Langmuir relation is used to describe how evaporation rates of the binary KCl-NaCl system change with time. The effective evaporation coefficient (α), which is a ratio of the actual evaporation rate to the theoretical maximum, was obtained for the KCl-NaCl system using this model. In the temperature range of 640 C to 760 C, the effective evaporation coefficient ranges from ∼0.4 to 0.1 for evaporation experiments conducted at 0.13 Pa. At temperatures below the melting point, the lower evaporation coefficients are suggested to result from the more complex path that a molecule needs to follow before escaping to the gas phase. At the higher liquid temperatures, the decreasing evaporation coefficients result from a combination of the increasing vapor-flow resistances and the heat-transfer effects at the evaporation surface and the condensate layer. The microanalysis of the condensate verified that composition of the condensate changes with time, consistent with the model calculation. The microstructural examination revealed that the vaporate may have condensed as a single solution phase, which upon cooling forms fine lamellar structures of the equilibrium KCl and NaCl phases. In conclusion, the optimum design of the evaporation process and equipment must take the mass and heat transfer factors and equipment materials issues into consideration

LiCl-KCl-UCl3 Salt production and Transfer for the Uranium Electrorefining

International Nuclear Information System (INIS)

Woo, Moon Sik; Kang, Hee Suk; Lee, Han Soo

2009-01-01

A pyrometallurgical partitioning technology to recover uranium from an uranium-TRU mixture which is the product material of electroreduction system is being developed at KAERI since 1997. In the process, the reactor of an electrorefiner consists of the electrodes and the molten chloride salt which is LiCl-KCl-UCl 3 . The role of uranium chloride salt (UCl 3 ) is to stabilize the initial cell voltage between electrodes in the electrorefining reactor. The process to produce a uranium chloride salt includes two steps: a reaction process of gaseous chlorine with liquid cadmium to form the CdCl 2 occurring in a Cd layer, followed by a process to produce UCl 3 by the reaction of U in the LiCl-KCl eutectic salt and CdCl 2 . The apparatus for producing UCl 3 consists of a chlorine gas generator, a chlorinator, and a off-gas wet scrubber. The temperature of the reactants are maintained at about 600 .deg. C . After the reaction is completed, the product salt is transferred from the vessel to the electrorefiner by a transfer system

Structure of halophilic malate dehydrogenase in multimolar KCl solutions from neutron scattering and ultracentrifugation

International Nuclear Information System (INIS)

Calmettes, P.

1987-01-01

The structure and solvent interactions of malate dehydrogenase from Halobacterium marismortui in multimolar KCl solvents are found to be similar to those in multimolar NaCl solvents reported previously (G. Zaccai, E. Wachtel and H. Eisenberg, J. Mol. Biol. 190 (1986) 97). KCl rather than NaCl is predominant in physiological medium. At salt concentrations up to about 3.0 M, the protein (a dimer of M 87000 g/mol) can be considered to occupy an invariant volume in which it is associated with about 4100 molecules of water and about 520 molecules of salt. At very low resolution, the enzyme particle appears to have a compact protein core and protruding protein parts in interaction with the water and salt components, structural features that are not observed in non-halophilic mitochondrial malate dehydrogenase. The above conclusions were drawn from the analysis of neutron scattering and ultracentrifugation data, and the complementarity of these approaches is discussed extensively. 24 refs.; 7 figs.; 4 tabs

Saturated steams pressure of HfCl4-KCl molten mixtures

International Nuclear Information System (INIS)

Salyulev, A.B.; Smirnov, M.V.; Kudyakov, V.Ya.

1980-01-01

A bellows null pressure gauge and the dynamic method were used to measure the total and partial pressures of saturated vapors of individual components of molten HfCl 4 -KCl mixtures, as a function of temperature (260 to 1000 deg C) and composition (1.9 to 64.3 mol.% HfCl 4 ). Empirical equations expressing the relationship between pressure and temperature are presented. It is shown that in molten mixtures of hafnium tetrachloride with chlorides of alkaline metals its partial pressure dramatically increases when potassium chloride substitutes for cesium chloride

Vacuum distillation for the separation of LiCl-KCl eutectic salt and cadmium in pyro process

International Nuclear Information System (INIS)

Kwon, S. W.; Park, K. M.; Lee, S. J.; Park, S. B.; Woo, M. S.; Kim, K. R.; Kim, J. G.; Ahn, D. H.; Lee, H. S.

2010-10-01

Electrorefining is a key step in pyro processing. Electrorefining process is generally composed of two recovery steps- a deposit of uranium onto a solid cathode (electrorefining) and then the recovery of the remaining uranium and Tru (Transuranic) elements simultaneously by a liquid cadmium cathode (electrowinning). In this study, distillation experiments of a LiCl-KCl eutectic salt and cadmium metal were carried out to examine the distillation behaviors for the development of the electrorefining and the electrowinning processes. The experimental set-up was composed of a distillation tower with an evaporator and a condenser, vacuum pump, control unit, and an off gas treatment system. The solid-liquid separation prior to distillation of the LiCl-KCl eutectic salt was proposed and found to be feasible for the reduction of the burden of the distillation process. The LiCl-KCl eutectic salt was successfully distilled after the liquid salt separation. Distillation experiments for cadmium metal were also carried out. The apparent evaporation rates of LiCl-KCl eutectic salt and cadmium increased with an increasing temperature. The evaporation behaviors of cadmium metal and cadmium-cerium alloy were compared. Cadmium in the alloy was successfully distilled and separated from cerium. The evaporation rate of cadmium in the alloy was lower than that of cadmium metal. The low evaporation rate of the alloy was probably caused by the formation of an intermetallic compound and the residual salt during the preparation of the alloy. Therefore, the distillation temperature for the distillation of the liquid cathode should be higher than the distillation of cadmium metal. The measured evaporation rates of the eutectic salt and cadmium were compared with the values calculated by a relation based on the kinetics of gases. The theoretical values of the evaporation rate calculated by the Hertz-Langmuir relation were higher than the experimental values. The deviations were compensated for

The importance of SO{sub 2} and SO{sub 3} for sulphation of gaseous KCl - An experimental investigation in a biomass fired CFB boiler

Energy Technology Data Exchange (ETDEWEB)

Kassman, Haakan [Vattenfall Power Consultant AB, Nykoeping (Sweden); Chalmers University of Technology, Department of Energy and Environment, Division of Energy Technology, Gothenburg (Sweden); Baefver, Linda [Technical Research Institute of Sweden, Energy Technology, Boraas (Sweden); Aamand, Lars-Erik [Chalmers University of Technology, Department of Energy and Environment, Division of Energy Technology, Gothenburg (Sweden)

2010-09-15

This paper is based on results obtained during co-combustion of wood pellets and straw in a 12 MW circulating fluidised bed (CFB) boiler. Elemental sulphur (S) and ammonium sulphate ((NH{sub 4}){sub 2}SO{sub 4}) were used as additives to convert the alkali chlorides (mainly KCl) to less corrosive alkali sulphates. Their performance was then evaluated using several measurement tools including, IACM (on-line measurements of gaseous alkali chlorides), a low-pressure impactor (particle size distribution and chemical composition of extracted fly ash particles), and deposit probes (chemical composition in deposits collected). The importance of the presence of either SO{sub 2} or SO{sub 3} for gas phase sulphation of KCl is also discussed. Ammonium sulphate performed significantly better than elemental sulphur. A more efficient sulphation of gaseous KCl was achieved with (NH{sub 4}){sub 2}SO{sub 4} even when the S/Cl molar ratio was less than half compared to sulphur. Thus the presence of gaseous SO{sub 3} is of greater importance than that of SO{sub 2} for the sulphation of gaseous KCl. (author)

Modernization at the Y-12 National Security Complex: A Case for Additional Experimental Benchmarks

Energy Technology Data Exchange (ETDEWEB)

Thornbury, M. L. [Y-12 National Security Complex, Oak Ridge, TN (United States); Juarez, C. [Y-12 National Security Complex, Oak Ridge, TN (United States); Krass, A. W. [Y-12 National Security Complex, Oak Ridge, TN (United States)

2017-08-14

Efforts are underway at the Y-12 National Security Complex (Y-12) to modernize the recovery, purification, and consolidation of un-irradiated, highly enriched uranium metal. Successful integration of advanced technology such as Electrorefining (ER) eliminates many of the intermediate chemistry systems and processes that are the current and historical basis of the nuclear fuel cycle at Y-12. The cost of operations, the inventory of hazardous chemicals, and the volume of waste are significantly reduced by ER. It also introduces unique material forms and compositions related to the chemistry of chloride salts for further consideration in safety analysis and engineering. The work herein briefly describes recent investigations of nuclear criticality for 235UO2Cl2 (uranyl chloride) and 6LiCl (lithium chloride) in aqueous solution. Of particular interest is the minimum critical mass of highly enriched uranium as a function of the molar ratio of 6Li to 235U. The work herein also briefly describes recent investigations of nuclear criticality for 235U metal reflected by salt mixtures of 6LiCl or 7LiCl (lithium chloride), KCl (potassium chloride), and 235UCl3 or 238UCl3 (uranium tri-chloride). Computational methods for analysis of nuclear criticality safety and published nuclear data are employed in the absence of directly relevant experimental criticality benchmarks.

Electrochemical behaviour of dysprosium in the eutectic LiCl-KCl at W and Al electrodes

International Nuclear Information System (INIS)

Castrillejo, Y.; Bermejo, M.R.; Barrado, A.I.; Pardo, R.; Barrado, E.; Martinez, A.M.

2005-01-01

The electrochemical behaviour of DyCl 3 was studied in the eutectic LiCl-KCl at different temperatures. The cathodic reaction can be written:Dy(III)+3e-bar Dy(0)which can be divided in two very close cathodic steps:Dy(III)+1e-bar Dy(II)andDy(II)+2e-bar Dy(0)Transient electrochemical techniques, such as cyclic voltammetry, chronopotentiometry, and chronoamperometry were used in order to study the reaction mechanism and the transport parameters of electroactive species at a tungsten electrode. The results showed that in the eutectic LiCl-KCl, electrocrystallization of dysprosium seems to be the controlling electrochemical step. Chronoamperometric studies indicated instantaneous nucleation of dysprosium with three dimensional growth of the nuclei whatever the applied overpotential.Mass transport towards the electrode is a simple diffusion process, and the diffusion coefficient of the electroactive species, i.e. Dy(III), has been calculated. The validity of the Arrhenius law was also verified by plotting the variation of the logarithm of the diffusion coefficient versus 1/T.In addition, the electrode reactions of the LiCl-KCl-DyCl 3 solutions at an Al wire were also investigated by cyclic voltammetry and open circuit chronopotentiometry. The redox potential of the Dy(III)/Dy couple at the Al electrode was observed at more positive potentials values than those at the inert electrode. This potential shift was thermodynamically analyzed by a lowering of activity of Dy in the metal phase due to the formation of intermetallic compounds

High-pressure melting curve of KCl: Evidence against lattice-instability theories of melting

International Nuclear Information System (INIS)

Ross, M.; Wolf, G.

1986-01-01

We show that the large curvature in the T-P melting curve of KCl is the result of a reordering of the liquid to a more densely packed arrangement. As a result theories of melting, such as the instability model, which do not take into account the structure of the liquid fail to predict the correct pressure dependence of the melting curve

Method for making a Pellet-type LiCl-KCl-UCl3 SALT

International Nuclear Information System (INIS)

Woo, M. S.; JIN, H. J.; Lee, H. S.; Kim, J. G.

2012-01-01

A pyrometallurgical partitioning technology to recover uranium from a uranium-TRU mixture which is the product material of electroreduction system is being developed at KAERI since 1997. In the process, the reactor of an electrorefiner consists of the electrodes and the molten chloride salt which is LiCl-KCl-UCl 3 . The role of uranium chloride salt (UCl 3 ) is to stabilize the initial cell voltage between electrodes in the electrorefining reactor. The process to produce a uranium chloride salt includes two steps: a reaction process of gaseous chlorine with liquid cadmium to form CdCl 2 occurring in a Cd layer, followed by a process to produce UCl 3 by the reaction of U in the LiCl-KCl eutectic salt and CdCl 2 The apparatus for producing UCl 3 consists of a chlorine gas generator, a uranium chlorinator, a Cd distiller, the pelletizer, and a off-gas and a dry scrubber. The temperature of the reactants is maintained at about 600 .deg. C. After the reaction is completed in the uranium chlorinator, The salt products is transferred to the Cd distiller to decrease residual Cd concentration in the salts, and then salt is transferred to the mould of a pelletizer by a transfer system to make a pellet type salt

Stability of yttria-stabilized zirconia during pyroprocessing tests

Energy Technology Data Exchange (ETDEWEB)

Choi, Eun-Young, E-mail: eychoi@kaeri.re.kr; Lee, Jeong; Lee, Sung-Jai; Kim, Sung-Wook; Jeon, Sang-Chae; Cho, Soo Haeng; Oh, Seung Chul; Jeon, Min Ku; Lee, Sang Kwon; Kang, Hyun Woo; Hur, Jin-Mok

2016-07-15

In this study, the feasibility of yttria-stabilized zirconia (YSZ) was investigated for use as a ceramic material, which can be commonly used for both electrolytic reduction and electrorefining. First, the stability of YSZ in salts for electrolytic reduction and electrorefining was examined. Then, its stability was demonstrated by a series of pyroprocessing tests, such as electrolytic reduction, LiCl distillation, electrorefining, and LiCl−KCl distillation, using a single stainless steel wire mesh basket containing fuel and YSZ. A single basket was used by its transportation from one test to subsequent tests without the requirements for unloading.

Saturated vapor pressure over molten mixtures of GaCl{sub 3} and alkali metal chlorides; Davlenie nasyshchennykh parov rasplavlennykh smesej CaCl{sub 3} s khloridami shchelochnykh metallov

Energy Technology Data Exchange (ETDEWEB)

Salyulev, A B; Smolenskij, V V; Moskalenko, N I [UrO RAN, Inst. Vysokotemperaturnoj Ehlektrokhimii, Elaterinburg (Russian Federation)

2004-07-01

Volatilities of GaCl{sub 3} and alkali metal chlorides over diluted (up to 3 mol %) solutions of GaCl{sub 3} in LiCl, NaCl, KCl, RbCl, and CsCl were measured at 1100 K by dynamic and indirect static methods. Chemical composition of saturated vapor over the mixed melts was determined. Partial pressures of the components were calculated. Their values depend essentially on specific alkali metal cation and on concentration of GaCl{sub 3}; their variation permits altering parameters of GaCl{sub 3} distillation from the salt melt in a wide range.

Contribution to knowledge of radiation damage in KCl crystals doped with Sr

International Nuclear Information System (INIS)

Sordi, G.-M.A.A.

1974-11-01

The radiation damages in KCl crystals doped with Sr ++ using thermo-ionic technique (ITC) and optical absorption measurements were studied. The variation of the entropy for the dipole jump starting from results reported by several authors was calculated. The irradiation effects with three different exposures were analysed: irradiation with gamma rays; irradiation with fast neutrons added to gamma irradiation; and irradiation with thermal neutrons together with fast neutrons and gamma rays. (Author) [pt

Electrochemical behavior of Th(IV) and its electrodeposition from ThF_4-LiCl-KCl melt

International Nuclear Information System (INIS)

Wang, Xianbin; Huang, Wei; Gong, Yu; Jiang, Feng; Zheng, Haiyang; Zhu, Tiejian; Long, Dewu; Li, Qingnuan

2016-01-01

The electrochemical behavior of Th(IV) ion on molybdenum (Mo) electrode was studied by cyclic voltammetry (CV) and square wave voltammetry (SWV) technologies at 773 K in ThF_4-LiCl-KCl melt. The reduction of Th(IV) to metal Th at −1.67 V (vs. Ag/AgCl) is a four-electron exchange process, which is quasi-reversible and diffusion-controlled. The diffusion coefficient (D) and activation energy of diffusion process for Th(IV) were determined to be 3.77 × 10"−"5 cm"2 s"−"1 and 59.2 kJ mol"−"1. The pulse potential electrolysis of ThF_4-LiCl-KCl melt revealed that 86.8% of Th(IV) can be separated from the melt based on the inductively coupled plasma atomic emission spectrometer (ICP-AES) results.

Conversion of KCl into KBH4 by Mechano-Chemical Reaction and its Catalytic Decomposition

Science.gov (United States)

Bilen, Murat; Gürü, Metin; Çakanyildirim, Çetin

2017-07-01

Production of KBH4, in the presence of KCl, B2O3 and MgH2 by means of a mechanical reaction and a dehydrogenation kinetic, constitute the main parts of this study. Operating time and reactant ratio are considered as two parameters for the mechanical reaction to obtain the maximum yield. The production process was carried out in a ball milling reactor, and the product residue was purified with ethylene diamine (EDA) and subsequently characterized by Fourier Transform Infrared Spectroscopy (FT-IR) and x-ray Diffraction (XRD) analyses. Optimum time for mechano-chemical treatment and reactant ratio (MgH2/KCl) were obtained as 1000 min and 1.0, respectively. Synthesized and commercial KBH4 were compared by hydrolysis tests in the presence of Co1-xNix/Al2O3 heterogeneous catalyst. Hydrogen generation rates, activation energy and order of the KBH4 decomposition reaction were obtained as 1578 {mL}_{{{{H}}2 }} \\min^{ - 1} {g}_{{catalyst}}^{ - 1}, 39.2 kJ mol-1 and zero order, respectively.

Capture and Solidification of Rare Earth Nuclide (Nd) in LiCl-KCl Eutectic Salt Using a Synthetic Inorganic Composite

Energy Technology Data Exchange (ETDEWEB)

Kim, Na-Young; Eun, Hee-Chul; Park, Hwan-Seo; Ahn, Do-Hee [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2017-06-15

In this study, neodymium (Nd) nuclides in LiCl-KCl eutectic salts were captured and solidified using a synthetic inorganic composite (Li{sub 2}O-SiO{sub 2}-Al{sub 2}O{sub 3}-B{sub 2}O{sub 3}), a process that allows the selective capture of Nd and fabrication of a composite with Nd captured from waste, without additional additives or mixing. The Nd nuclides in the LiCl-KCl eutectic salt were mainly captured in the form of LiNdSiO{sub 4}, and it was confirmed that NdSiO{sub 3} can be formed in the composite with captured Nd when the content of Nd in the composite is increased. The capture efficiency was higher than about 98 wt%. It was thought that the salt recovered from the Nd capture test was a renewable form could be reused in the pyroprocessing of used nuclear fuel, because the composite has high chemical durability in a LiCl-KCl eutectic salt at 900 ℃. The composite captured Nd was fabricated into a homogeneous glass form and a stable ceramic form.

Corrosion behavior induced by LiCl-KCl in type 304 and 316 stainless steel and copper at low temperature

Energy Technology Data Exchange (ETDEWEB)

Sim, Jee Hyung; Kim, Yong Soo; Cho, Il Je [Dept. of Nuclear Engineering, Hanyang University, Seoul (Korea, Republic of)

2017-06-15

The corrosion behavior of stainless steel (304 and 316 type) and copper induced by LiCl-KCl at low temperatures in the presence of sufficient oxygen and moisture was investigated through a series of experiments (at 30°C, 40°C, 60°C, and 80°C for 24 hours, 48 hours, 72 hours, and 96 hours). The specimens not coated on one side with an aqueous solution saturated with LiCl-KCl experienced no corrosion at any temperature, not even when the test duration exceeded 96 hours. Stainless steel exposed to LiCl-KCl experienced almost no corrosion below 40°C, but pitting corrosion was observed at temperatures above 60°C. As the duration of the experiment was increased, the rate of corrosion accelerated in proportion to the temperature. The 316 type stainless steel exhibited better corrosion resistance than did the 304 type. In the case of copper, the rate of corrosion accelerated in proportion to the duration and temperature but, unlike the case of stainless steel, the corrosion was more general. As a result, the extent of copper corrosion was about three times that of stainless steel.

Characterization Ag/AgCl reference electrode by U/U3+ equilibrium potential measurements in LiCl-KCl eutectic melt

International Nuclear Information System (INIS)

Kobayashi, Fumiaki; Kitawaki, Shinichi; Amamoto, Ippei; Igarashi, Miyuki

1999-02-01

The Ag/ AgCl reference electrode is often used in electrochemical measurements of molten chloride system. By measuring the U/U 3+ equilibrium potential in the cell, U(s) | UCl 3 , LiCl-KCl parallel LiCl-KCl, Ag + | Ag (s), the characterization of the Ag/AgCl reference electrode was made. The behavior of two types of reference electrode having either a mullite or a Pyrex-glass membrane bridge was examined. It was confirmed that the two types of reference electrode can be regarded as almost equivalent. The reproducibility of the reading from the electrodes having the identical construction was showing to be within 0.003 V. (author)

Polarographic investigation of complexing kinetics of polyacrylate anions with cadmium ions. Polyarograficheskoe issledovanie kinetiki kompleksoobrazovaniya poliakrilat-anionov s ionami kadmiya

Energy Technology Data Exchange (ETDEWEB)

Avlyanov, Zh K; Kabanov, N M; Zezin, A B; Askarov, M A

1990-01-01

The processes which occur during the reduction of cadmium ions from polymer-metallic complexes (PMC) are studied for the purposes of polarographic investigation of complexing kinetics of polyacrylate anions (PAA) of different molecular masses with cadmium ions in KCl aqueous solutions. An expression is derived for establishing semiwave potential. PMC formation and dissociation reduction rate constants are calculated. It is shown that intramolecular reorderings required for the formation of a two-coordinate complex proceed much slower as compared to the diffusion of free ions.

Saturated steams pressure of HfCl/sub 4/-KCl molten mixtures

Energy Technology Data Exchange (ETDEWEB)

Salyulev, A B; Smirnov, M V; Kudyakov, V Ya [AN SSSR, Sverdlovsk. Inst. Ehlektrokhimii

1980-02-01

A bellows null pressure gauge and the dynamic method were used to measure the total and partial pressures of saturated vapors of individual components of molten HfCl/sub 4/-KCl mixtures, as a function of temperature (260 to 1000 deg C) and composition (1.9 to 64.3 mol.% HfCl/sub 4/). Empirical equations expressing the relationship between pressure and temperature are presented. It is shown that in molten mixtures of hafnium tetrachloride with chlorides of alkaline metals its partial pressure dramatically increases when potassium chloride substitutes for cesium chloride.

Absorption of water vapour in the falling film of water-(LiBr + LiI + LiNO{sub 3} + LiCl) in a vertical tube at air-cooling thermal conditions

Energy Technology Data Exchange (ETDEWEB)

Bourouis, Mahmoud; Valles, Manel; Medrano, Marc; Coronas, Alberto [Centro de Innovacion Tecnologica en Revalorizacion Energetica y Refrigeracion, CREVER, Universitat Rovira i Virgili, Autovia de Salou, s/n, 43006, Tarragona (Spain)

2005-05-01

In air-cooled water-LiBr absorption chillers the working conditions in the absorber and condenser are shifted to higher temperatures and concentrations, thereby increasing the risk of crystallisation. To develop this technology, two main problems are to be addressed: the availability of new salt mixtures with wider range of solubility than water-LiBr, and advanced absorber configurations that enable to carry out simultaneously an appropriate absorption process and an effective air-cooling. One way of improving the solubility of LiBr aqueous solutions is to add other salts to create multicomponent salt solutions. The aqueous solution of the quaternary salt system (LiBr + LiI + LiNO{sub 3} + LiCl) presents favourable properties required for air-cooled absorption systems: less corrosive and crystallisation temperature about 35 K lower than that of water-LiBr.This paper presents an experimental study on the absorption of water vapour over a wavy laminar falling film of an aqueous solution of (LiBr + LiI + LiNO{sub 3} + LiCl) on the inner wall of a water-cooled smooth vertical tube. Cooling water temperatures in the range 30-45 C were selected to simulate air-cooling thermal conditions. The results are compared with those obtained in the same experimental set-up with water-LiBr solutions.The control variables for the experimental study were: absorber pressure, solution Reynolds number, solution concentration and cooling water temperature. The parameters considered to assess the absorber performance were: absorber thermal load, mass absorption flux, degree of subcooling of the solution leaving the absorber, and the falling film heat transfer coefficient.The higher solubility of the multicomponent salt solution makes possible the operation of the absorber at higher salt concentration than with the conventional working fluid water-LiBr. The absorption fluxes achieved with water-(LiBr + LiI + LiNO{sub 3} + LiCl) at a concentration of 64.2 wt% are around 60 % higher than

Characterization of Niobium Platings Obtained from NaCl-KCl Melts

DEFF Research Database (Denmark)

Gillesberg, Bo; Barner, Jens H. Von; Bjerrum, Niels

1998-01-01

-uniform in thickness. At temperatures below 550°C no niobium metal could be identified in the product.When metallic nickel was used as substrate intermetallic compounds (e.g. NbNi3) were formed in the interface between the substrate and the deposit. This resulted in poor adherence of the deposit. In the case of AISI......316 stainless steel substrates no intermetallic phases were observed. Further an excellent adhesion of the deposited niobium layer was obtained.Deposits (on nickel substrates) from NaCl-KCl melts at 750°C with oxide added (molar ratio O/Nb greater than 0.5) were thin and consisted of niobium...

Fabrication and Application of (1-x) NaCl+xKCl Solid Solution

International Nuclear Information System (INIS)

Kyi Kyi Lwin

2011-12-01

(1-X)NaCl+xKCl solid solution are prepared by the starting materials NaCl (0.9, 0.95) in equal molar ratio. The solid solutions are heat-treated at various temperature and XRD analyses are carried out for the solid solutions to examine the crystalline phase, crystallographic orientation and lattice parameters. The electrical properties of the solutions are determined by using the conductometer. The solid solutions are utilized as crystal oscillator and outcoming frequencies, capacitances and dielectric constants are also investigated.

Interplay between structure and transport properties of molten salt mixtures of ZnCl2-NaCl-KCl: A molecular dynamics study.

Science.gov (United States)

Manga, Venkateswara Rao; Swinteck, Nichlas; Bringuier, Stefan; Lucas, Pierre; Deymier, Pierre; Muralidharan, Krishna

2016-03-07

Molten mixtures of network-forming covalently bonded ZnCl2 and network-modifying ionically bonded NaCl and KCl salts are investigated as high-temperature heat transfer fluids for concentrating solar power plants. Specifically, using molecular dynamics simulations, the interplay between the extent of the network structure, composition, and the transport properties (viscosity, thermal conductivity, and diffusion) of ZnCl2-NaCl-KCl molten salts is characterized. The Stokes-Einstein/Eyring relationship is found to break down in these network-forming liquids at high concentrations of ZnCl2 (>63 mol. %), while the Eyring relationship is seen with increasing KCl concentration. Further, the network modification due to the addition of K ions leads to formation of non-bridging terminal Cl ions, which in turn lead to a positive temperature dependence of thermal conductivity in these melts. This new understanding of transport in these ternary liquids enables the identification of appropriate concentrations of the network formers and network modifiers to design heat transfer fluids with desired transport properties for concentrating solar power plants.

Synthesis and photocatalytic activity of poly(triazine imide)

KAUST Repository

Ham, Yeilin; Maeda, Kazuhiko; Cha, Dong Kyu; Takanabe, Kazuhiro; Domen, Kazunari

2012-01-01

Poly(triazine imide) was synthesized with incorporation of Li+ and Cl- ions (PTI/Li+Cl-) to form a carbon nitride derivative. The synthesis of this material by the temperature-induced condensation of dicyandiamide was examined both in a eutectic mixture of LiCl-KCl and without KCl. On the basis of X-ray diffraction measurements of the synthesized materials, we suggest that a stoichiometric amount of LiCl is necessary to obtain the PTI/Li+Cl- phase without requiring the presence of KCl at 873 K. PTI/Li+Cl- with modification by either Pt or CoOx as cocatalyst photocatalytically produced H2 or O2, respectively, from water. The production of H2 or O2 from water indicates that the valence and conduction bands of PTI/Li+Cl- were properly located to achieve overall water splitting. The treatment of PTI/Li +Cl- with [Pt(NH3)4]2+ cations enabled the deposition of Pt through ion exchange, demonstrating photocatalytic activity for H2 evolution, while treatment with [PtCl6]2- anions resulted in no Pt deposition. This was most likely because of the preferential exchange between Li+ ions and [Pt(NH3)4]2+ cations. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Synthesis and photocatalytic activity of poly(triazine imide)

KAUST Repository

Ham, Yeilin

2012-10-22

Poly(triazine imide) was synthesized with incorporation of Li+ and Cl- ions (PTI/Li+Cl-) to form a carbon nitride derivative. The synthesis of this material by the temperature-induced condensation of dicyandiamide was examined both in a eutectic mixture of LiCl-KCl and without KCl. On the basis of X-ray diffraction measurements of the synthesized materials, we suggest that a stoichiometric amount of LiCl is necessary to obtain the PTI/Li+Cl- phase without requiring the presence of KCl at 873 K. PTI/Li+Cl- with modification by either Pt or CoOx as cocatalyst photocatalytically produced H2 or O2, respectively, from water. The production of H2 or O2 from water indicates that the valence and conduction bands of PTI/Li+Cl- were properly located to achieve overall water splitting. The treatment of PTI/Li +Cl- with [Pt(NH3)4]2+ cations enabled the deposition of Pt through ion exchange, demonstrating photocatalytic activity for H2 evolution, while treatment with [PtCl6]2- anions resulted in no Pt deposition. This was most likely because of the preferential exchange between Li+ ions and [Pt(NH3)4]2+ cations. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Experimental observations on electrorefining spent nuclear fuel in molten LiCl-KCl/liquid cadmium system

International Nuclear Information System (INIS)

Johnson, T. A.; Laug, D. V.; Li, S. X.; Sofu, T.

1999-01-01

Argonne National Laboratory (ANL) is currently performing a demonstration program for the Department of Energy (DOE) which processes spent nuclear fuel from the Experimental Breeder Reactor (EBR-II). One of the key steps in this demonstration program is electrorefining of the spent fuel in a molten LiCl-KCl/liquid cadmium system using a pilot scale electrorefiner (Mk-IV ER). This article summarizes experimental observations and engineering aspects for electrorefining spent fuel in the molten LiCl-KCl/liquid cadmium system. It was found that the liquid cadmium pool acted as an intermediate electrode during the electrorefining process in the ER. The cadmium level was gradually decreased due to its high vapor pressure and vaporization rate at the ER operational temperature. The low cadmium level caused the anode assembly momentarily to touch the ER vessel hardware, which generated a periodic current change at the salt/cathode interface and improved uranium recovery efficiency for the process. The primary current distributions calculated by numerical simulations were used in interpreting the experimental results

[Serial change of perilymphatic potassium ion concentration in the scala tympani after introducing KCl-solution into the guinea pigs' tympanic cavity].

Science.gov (United States)

Ikeno, K

1990-09-01

Characteristic nystagmus similar to the Meniere's attack could be observed after introducing KCl solution into the tympanic cavity of guinea pigs. To confirm the fact that this nystagmus was provoked by the high perilymphatic potassium ion concentration, the K+ activity of perilymph was recorded serially through the K+ specific microelectrode inserted into the scala tympani. The rapid increment of K+ activity reached maximum at 120 minutes after introducing KCl solution, and then it decreased gradually to a half of the maximum activity. However, such change of perilymphatic potassium ion concentration was not observed by introducing sucrose solution as control.

Making a Pellet-type LiCl-KCl-UCl3 salt for Electrorefining

Energy Technology Data Exchange (ETDEWEB)

Woo, M. S.; Jin, H. J.; Kim, I. T.; Kim, J. G. [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2013-05-15

The role of uranium chloride salt (UCl3) is to stabilize the initial cell voltage between electrodes in the electrorefining reactor. The process to produce a uranium chloride salt includes two steps: a reaction process of gaseous chlorine with liquid cadmium to form the CdCl2 occurring in a Cd layer, followed by a process to produce UCl3 by the reaction of U in the LiCl-KCl eutectic salt and CdCl2 The apparatus for producing UCl3 consists of a chlorine gas generator, a uranium chlorinator, a Cd distiller, the pelletizer, and a off-gas and a dry scrubber. The temperature of the reactants is maintained at about 600 .deg. C. After the reaction is completed in the uranium chlorinator, The salt products is transferred to the Cd distiller to decrease residual Cd concentration in the salts, and then salt is transferred to the mould of pelletizer by a transfer system to make pellet type salt. Making pellet type LiCl-KCl-UCl3 salt for electrorefining was carried out using the chlorinator, Cd distiller, and pelletizer. Salt transfer carried out by salt transfer equipment heated 500 .deg. C. The Cd concentration of final salt products distillated at 60 torr, 2 hrs, 600 .deg. C was 200 ppm from the ICP, XRD analysis. And pellet type salt products were fabricated by using the mould of pelletizer at 90∼130 .deg. C.

Making a Pellet-type LiCl-KCl-UCl3 salt for Electrorefining

International Nuclear Information System (INIS)

Woo, M. S.; Jin, H. J.; Kim, I. T.; Kim, J. G.

2013-01-01

The role of uranium chloride salt (UCl3) is to stabilize the initial cell voltage between electrodes in the electrorefining reactor. The process to produce a uranium chloride salt includes two steps: a reaction process of gaseous chlorine with liquid cadmium to form the CdCl2 occurring in a Cd layer, followed by a process to produce UCl3 by the reaction of U in the LiCl-KCl eutectic salt and CdCl2 The apparatus for producing UCl3 consists of a chlorine gas generator, a uranium chlorinator, a Cd distiller, the pelletizer, and a off-gas and a dry scrubber. The temperature of the reactants is maintained at about 600 .deg. C. After the reaction is completed in the uranium chlorinator, The salt products is transferred to the Cd distiller to decrease residual Cd concentration in the salts, and then salt is transferred to the mould of pelletizer by a transfer system to make pellet type salt. Making pellet type LiCl-KCl-UCl3 salt for electrorefining was carried out using the chlorinator, Cd distiller, and pelletizer. Salt transfer carried out by salt transfer equipment heated 500 .deg. C. The Cd concentration of final salt products distillated at 60 torr, 2 hrs, 600 .deg. C was 200 ppm from the ICP, XRD analysis. And pellet type salt products were fabricated by using the mould of pelletizer at 90∼130 .deg. C

Distribution behavior of uranium, neptunium, rare-earth elements (Y, La, Ce, Nd, Sm, Eu, Gd) and alkaline-earth metals (Sr,Ba) between molten LiCl-KCl eutectic salt and liquid cadmium or bismuth

International Nuclear Information System (INIS)

Kurata, M.; Sakamura, Y.; Hijikata, T.; Kinoshita, K.

1995-01-01

Distribution coefficients of uranium neptunium, eight rare-earth elements (Y, La, Ce, Pr, Nd, Sm, Eu and Gd) and two alkaline-earth metals (Sr and Ba) between molten LiCl-KCl eutectic salt and either liquid cadmium or bismuth were measured at 773 K. Separation factors of trivalent rare-earth elements to uranium or neptunium in the LiCl-KCl/Bi system were by one or two orders of magnitude larger than those in the LiCl-KCl/Cd system. On the contrary, the separation factors of alkaline-earth metals and divalent rare-earth elements to trivalent rare-earth elements were by one or two orders of magnitude smaller in the LiCl-KCl/Bi system. (orig.)

Testing of pyrochemical centrifugal contactors

International Nuclear Information System (INIS)

Chow, L.S.; Carls, E.L.; Basco, J.K.; Johnson, T.R.

1996-01-01

A centrifugal contactor that performs oxidation and reduction exchange reactions between molten metals and salts at 500 degrees Centigrade has been tested successfully at Argonne National Laboratory (ANL). The design is based on contactors for aqueous- organic systems operation near room temperature. In tests to demonstrate the performance of the pyrocontactor, cadmium and LICl-KCl eutectic salt were the immiscible solvent phases, and rare earths were the distributing solutes. The tests showed that the pyrocontactor mixed and separated the phases well, with stage efficiencies approaching 99% at rotor speeds near 2700 rpm. The contactor ran smoothly and reliably over the entire range of speeds that was tested

Relação entre o alumínio extraível com KCl e oxalato de amônio e a mineralogia da fração argila, em solos ácidos brasileiros

Directory of Open Access Journals (Sweden)

Gabriel Octávio de Mello Cunha

2014-10-01

Full Text Available Em solos ácidos de ambiente mais tropical com esmectitas, assim como em solos altamente tamponados de ambiente subtropical, contendo esmectita com hidroxi-Al entrecamadas (EHE e, ou, vermiculita com hidroxi-Al entrecamadas (VHE, os teores de Al-KCl podem ser excepcionalmente altos; entretanto, em alguns casos não se manifestam efeitos fitotóxicos do elemento nas culturas. O Al "trocável" é tradicionalmente quantificado no extrato da solução de KCl 1 mol L-1 (Al-KCl, mas nem sempre esse elemento provém unicamente de formas trocáveis. Este trabalho objetivou investigar relações entre o Al extraído com solução de KCl e de oxalato de amônio com a mineralogia da fração argila. A quantificação do Al nos extratos de KCl e oxalato de amônio foi feita, respectivamente, por titulação com NaOH 0,02 mol L-1 padronizado e por espectrofotometria de absorção atômica. Foram utilizadas amostras de dois horizontes (A e B de 12 perfis de solo de cinco estados brasileiros (AC, PE, BA, RS e SC, com diferentes características mineralógicas, todos com teores de Al-KCl superior a 4 cmol c kg-1 no horizonte B. Dois perfis de SC (Rancho Queimado e Curitibanos, com níveis mais baixos de Al-KCl, foram incluídos para comparação. Os altos teores de Al-KCl evidenciaram-se relacionados com a mineralogia dos solos estudados. Nos solos ácidos com mais esmectitas, drenagem moderada ou imperfeita e oscilação do lençol freático houve evidências morfológicas, confirmadas pelas análises mineralógicas, de que no clima atual ocorre um processo de destruição de argilas, liberando Al que precipita como compostos amorfos. A alta concentração salina da solução de KCl dissolve parcialmente tais compostos, superestimando as formas trocáveis desse elemento, principalmente nos horizontes subsuperficiais. Nos solos ácidos do ambiente subtropical, os teores de Al-KCl também foram altos, embora com valores mais baixos do que nos com predomínio de

Method for making a Pellet-type LiCl-KCl-UCl{sub 3} SALT

Energy Technology Data Exchange (ETDEWEB)

Woo, M. S.; JIN, H. J.; Lee, H. S.; Kim, J. G. [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2012-05-15

A pyrometallurgical partitioning technology to recover uranium from a uranium-TRU mixture which is the product material of electroreduction system is being developed at KAERI since 1997. In the process, the reactor of an electrorefiner consists of the electrodes and the molten chloride salt which is LiCl-KCl-UCl{sub 3}. The role of uranium chloride salt (UCl{sub 3}) is to stabilize the initial cell voltage between electrodes in the electrorefining reactor. The process to produce a uranium chloride salt includes two steps: a reaction process of gaseous chlorine with liquid cadmium to form CdCl{sub 2} occurring in a Cd layer, followed by a process to produce UCl{sub 3} by the reaction of U in the LiCl-KCl eutectic salt and CdCl{sub 2} The apparatus for producing UCl{sub 3} consists of a chlorine gas generator, a uranium chlorinator, a Cd distiller, the pelletizer, and a off-gas and a dry scrubber. The temperature of the reactants is maintained at about 600 .deg. C. After the reaction is completed in the uranium chlorinator, The salt products is transferred to the Cd distiller to decrease residual Cd concentration in the salts, and then salt is transferred to the mould of a pelletizer by a transfer system to make a pellet type salt

Production of strangeness in Ar+KCl reactions at 1.756 AGeV with HADES; Produktion von Seltsamkeit in Ar+KCl Reaktionen bei 1.756 AGeV mit HADES

Energy Technology Data Exchange (ETDEWEB)

Schmah, Alexander Marc

2008-05-15

In september/october 2005 the first of heavier colliding systems was investigated with the HADES spectrometer by using an Ar projectile and a KCl target at a bombarding energy of 1.756 AGeV. With 850 million semi-central reactions in the colliding system Ar+KCl the opportunity was given for one of the most extensive hadron analyses in the SIS energy regime. The results of these analyses are presented in this thesis. The main focal point is the production of particles with strangeness content. The particle ratios of {lambda} and K{sup 0}{sub S} are comparable to those of other experiments. The corrections of acceptance, detector-, cut- and reconstruction efficiency is done using the simulation packages PLUTO, UrQMD and GEANT. With the corrected transverse mass spectra rapidity distributions and particle multiplicities are calculated. Due to the nearly full sample of reconstructed particles carrying strangeness, one can conclude to the missing part, which is connected to the charged {sigma}-hyperons. Within the error bars the fraction of {sigma}{sup {+-}}{sup ,0} is at least 12 % of the {lambda} multiplicity. The detection of the {phi} vector meson far below the nucleon-nucleon production threshold in the decay channel {phi} {yields} K{sup +}K{sup -} exceeds with 168 {+-} 18 the only up to now published data by more than a factor 7. The extracted effective temperature of T{sub eff}=80{+-}9{sup +2}{sub -3} is a brand-new result. The determined {phi}/K{sup -} ratio is 0.59{sup +0.30}{sub -0.29}. (orig.)

Respon pertumbuhan bibit kakao (Theobroma cacao L.) terhadap pemberian pupuk guano dan KCl

OpenAIRE

Rajagukguk, Pispa

2015-01-01

Addition of Guano in Cultivation of Cacao Seedling is the one of step to use organic fertilizer that comes from animal feces in the world. For that purpose addition guano aims to increase growth of Cacao in Cultivation of Seedling. This research had been conducted at experimental field of Fakultas Pertanian USU in October 2013 - January 2014 using factorial randomized block design with two factor, i.e. addition dose of Guano (0, 75 , 150 , 225 g/polibag) and dose of KCl (0 , ...

Integrated Data Collection Analysis (IDCA) Program — KClO₃/Icing Sugar (-100 mesh) Mixture

Energy Technology Data Exchange (ETDEWEB)

Sandstrom, Mary M. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Brown, Geoffrey W. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Preston, Daniel N. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Pollard, Colin J. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Warner, Kirstin F. [Naval Surface Warfare Center (IHD-NSWC), Indian Head, MD (United States). Indian Head Division; Sorenson, Daniel N. [Naval Surface Warfare Center (IHD-NSWC), Indian Head, MD (United States). Indian Head Division; Remmers, Daniel L. [Naval Surface Warfare Center (IHD-NSWC), Indian Head, MD (United States). Indian Head Division; Moran, Jesse S. [Naval Surface Warfare Center (IHD-NSWC), Indian Head, MD (United States). Indian Head Division; Shelley, Timothy J. [Air Force Research Lab. (AFRL/RXQF), Tyndall AFB, FL (United States); Hsu, Peter C. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Whipple, Richard E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Reynolds, John G. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2011-05-02

The Integrated Data Collection Analysis (IDCA) program is conducting a proficiency study for Small-Scale Safety and Thermal (SSST) testing of homemade explosives (HMEs). Described here are the results for impact, friction, electrostatic discharge, and scanning calorimetry analysis of a mixture of KClO₃ sized through a 100-mesh sieve mixed with icing sugar, also sized through a 100-mesh sieve—KClO₃/icing sugar (-100) mixture. This material was selected because of the challenge of performing SSST testing of a mixture of two solid materials. The mixture was found to be: 1) more sensitive to impact than RDX, with sensitivity similar to PETN, 2) the same or more sensitive to friction than PETN, and 3) less sensitive to spark than RDX. The analysis showed that the mixture has thermally stability similar to RDX and is perhaps more energetic upon decomposition but variable results indicate sampling issues.

Rheed Investigation of Pd/Al Bimetallic System on KCl(001) Substrate

Science.gov (United States)

Masek, K.; Moroz, V.; Matolín, V.

Pd/Al alloys have very interesting properties from the point of view of their possible application in heterogeneous catalysis. Preparation of small heteroepitaxial Pd/Al alloy particles opens a new way in studies of the influence of Pd/Al crystallographic structure on the alloy catalytic properties. Pd/Al alloy particles were grown by the molecular beam epitaxy method. Their crystallographical structure was controlled by reflection high energy electron diffraction (RHEED). It was found that Pd deposited on epitaxial 3D Al particles grown on KCl is intermixing with Al. This process is accompanied by the variation of lattice parameter from the Al value to the Pd one.

Thermodynamic properties of thulium and ytterbium in fused NaCl-KCl-CsCl eutectic

Energy Technology Data Exchange (ETDEWEB)

Novoselova, A., E-mail: A.Novoselova@ihte.uran.ru [Institute of High-Temperature Electrochemistry, Ural Division, Russian Academy of Science, S. Kovalevskaya Str., 22, Ekaterinburg 620990 (Russian Federation); Smolenski, V. [Institute of High-Temperature Electrochemistry, Ural Division, Russian Academy of Science, S. Kovalevskaya Str., 22, Ekaterinburg 620990 (Russian Federation)

2011-07-15

Research highlights: > Tm and Yb chloride compounds as fission products. > The investigation of electrochemical properties of lanthanides. > Determination of the apparent standard redox potentials of the couple Ln(III)/Ln(II) in fused NaCl-KCl-CsCl eutectic at (823 to 973) K. > The calculation of the basic thermodynamic properties of redox reaction in molten salt. - Abstract: This work presents the results of a study of the Tm{sup 3+}/Tm{sup 2+} and Yb{sup 3+}/Yb{sup 2+} couple redox potentials vs. Cl{sup -}/Cl{sub 2} reference electrode at the temperature range (823 to 973) K in fused NaCl-KCl-CsCl eutectic by direct potentiometric method. Initial concentrations of TmCl{sub 3} and YbCl{sub 3} in solvents did not exceed 5.0 mol%. Basic thermodynamic properties of the reactions TmCl{sub 2(l)} + 1/2 Cl{sub 2(g)} {r_reversible} TmCl{sub 3(l)} and YbCl{sub 2(l)} + 1/2 Cl{sub 2(g)} {r_reversible} YbCl{sub 3(l)} were calculated using the temperature dependencies of apparent standard potentials of the couples E{sub Tm{sup 3+}/Tm{sup 2+*}} and E{sub Yb{sup 3+}/Yb{sup 2+*}}.

Successful Management of Tubal Ectopic Pregnancy with Transvaginal Sonography Guided Intracardiac KCL Injection and Systemic Methotrexate - A Case Report

Directory of Open Access Journals (Sweden)

Sumesh Choudhary

2014-01-01

Full Text Available Background: Methotrexate (Mtx is an accepted modality for conservative treatment of ectopic pregnancy. However, there is no consensus regarding its use in live ectopic pregnancy and high serum beta-human chorionic gonadotrophin (β-hCG titres. Concurrent use of intra-sac hypertonic KCl, to produce cardiac asystole with systemic Mtx potentially improve outcome in live ectopic gestations with very high serum β-hCG titres. Here a successful management of live ectopic pregnancy in a 25-year-old nulliparous woman, with very high β-hCG titres (29502.04mIU/mL, using ultrasound-guided intra-cardiac potassium chloride (KCl injection and systemic Mtx is reported. No treatment related complications were encountered. However, individualized treatment with a stringent follow-up regime is mandatory in such cases.

K-Cl cotransporters, cell volume homeostasis, and neurological disease.

Science.gov (United States)

Kahle, Kristopher T; Khanna, Arjun R; Alper, Seth L; Adragna, Norma C; Lauf, Peter K; Sun, Dandan; Delpire, Eric

2015-08-01

K(+)-Cl(-) cotransporters (KCCs) were originally characterized as regulators of red blood cell (RBC) volume. Since then, four distinct KCCs have been cloned, and their importance for volume regulation has been demonstrated in other cell types. Genetic models of certain KCCs, such as KCC3, and their inhibitory WNK-STE20/SPS1-related proline/alanine-rich kinase (SPAK) serine-threonine kinases, have demonstrated the evolutionary necessity of these molecules for nervous system cell volume regulation, structure, and function, and their involvement in neurological disease. The recent characterization of a swelling-activated dephosphorylation mechanism that potently stimulates the KCCs has pinpointed a potentially druggable switch of KCC activity. An improved understanding of WNK/SPAK-mediated KCC cell volume regulation in the nervous system might reveal novel avenues for the treatment of multiple neurological diseases. Copyright © 2015 Elsevier Ltd. All rights reserved.

Chemical forms of 35S in KCl crystals doped with elementary 35S. Pt. 1

International Nuclear Information System (INIS)

Maddock, A.G.; Todorovsky, D.S.

1983-01-01

KCl crystals have been doped with 35 S at low chemical concentrations. Upon solution of the doped crystals in cyanide solution and analysis by the method of Kasrai and Maddock, the 35 S appears in the same chemical forms as are found for the 35 S produced in similar crystals by the (n, p) reaction. Reactions are suggested whereby these products may be produced. (orig.)

Galvanic high temperature cell with solid negative electrode and an electrolyte melt. Galvanische Hochtemperaturzelle mit fester negativer Elektrode und einem Schmelzelektrolyten

Energy Technology Data Exchange (ETDEWEB)

Kappus, W; Borger, W

1987-01-08

The purpose of the invention is to make an electrolyte melt available for high temperature cells (e.g. LiFeS cells), which guarantees ion transport and also acts as a separator. The invention starts from the fact that binary melts of the LiCl/KCl type are only liquid (i.e. without solid components) at a certain temperature at certain concentrations. With suitable mixing conditions, which apart from a eutectic composition, are mainly on the side of one of the two components, one can ensure that this component is present in the solid phase. In this way, a solid framework of LiCl, for example, is formed between the electrode plates in situ as a separator, in the pores of which the excess melt (e.g. LiCl/KCl) can carry out ion conduction. The volumetric ratio of the electrolyte melt in which liquid and solid phases are present at the working temperature of the cell should preferably be in the range of 2:1 to 1:2.

An investigation of ruthenium coating from LiCl–KCl eutectic melt

International Nuclear Information System (INIS)

Kartal Sireli, G.

2014-01-01

Graphical abstract: - Highlights: • A white/gray Ru coating was achieved via electrodeposition from LiCl–KCl melt. • Cathodic current efficiency (η) was increased as high as 99.68%. • A dense and 8.5 μm thick Ru coating was possible to be grown after 2 h. • “Faceted structure” was observed on the surface of Ru deposited at 3 and 7 mA/cm 2 . • The thickness of Ru increased with increasing both current density and time. - Abstract: In this study, electrodeposition of ruthenium (Ru) from LiCl–KCl eutectic melt was investigated in a systematic manner and the effects of process parameters namely current density, time and agitation of electrolyte on the thickness and morphology of Ru layer were explored. The presence of Ru on graphite substrates was confirmed by thin film X-ray diffraction method. The Ru coatings formed at all electrodeposition conditions appeared as a white/gray deposit. The typical “faceted structure” was observed on the surface of Ru deposited at 3 and 7 mA/cm 2 . Fracture cross-section examinations revealed the columnar morphology of Ru which was twinned with boundaries. The smooth appearance of Ru coating became uneven and rough with coarse nodules at 12 mA/cm 2 . The thickness of Ru increased with increasing both current density and time at stationary electrodeposition conditions. A dense and 7.5 μm thick Ru coating was possible to grow on graphite without any agitation at 3 mA/cm 2 for 2 h. The highest cathodic current efficiency (η), 99.68%, was achieved at 3 mA/cm 2 after 2 h of electrodeposition time with the rotating cathode speed of 50 rpm. The cross sectional micro-indentation studies indicated that the Ru layer has hardness as high as 450 ± 10 HV

An investigation of ruthenium coating from LiCl–KCl eutectic melt

Energy Technology Data Exchange (ETDEWEB)

Kartal Sireli, G., E-mail: kartalgu@itu.edu.tr

2014-10-30

Graphical abstract: - Highlights: • A white/gray Ru coating was achieved via electrodeposition from LiCl–KCl melt. • Cathodic current efficiency (η) was increased as high as 99.68%. • A dense and 8.5 μm thick Ru coating was possible to be grown after 2 h. • “Faceted structure” was observed on the surface of Ru deposited at 3 and 7 mA/cm{sup 2}. • The thickness of Ru increased with increasing both current density and time. - Abstract: In this study, electrodeposition of ruthenium (Ru) from LiCl–KCl eutectic melt was investigated in a systematic manner and the effects of process parameters namely current density, time and agitation of electrolyte on the thickness and morphology of Ru layer were explored. The presence of Ru on graphite substrates was confirmed by thin film X-ray diffraction method. The Ru coatings formed at all electrodeposition conditions appeared as a white/gray deposit. The typical “faceted structure” was observed on the surface of Ru deposited at 3 and 7 mA/cm{sup 2}. Fracture cross-section examinations revealed the columnar morphology of Ru which was twinned with boundaries. The smooth appearance of Ru coating became uneven and rough with coarse nodules at 12 mA/cm{sup 2}. The thickness of Ru increased with increasing both current density and time at stationary electrodeposition conditions. A dense and 7.5 μm thick Ru coating was possible to grow on graphite without any agitation at 3 mA/cm{sup 2} for 2 h. The highest cathodic current efficiency (η), 99.68%, was achieved at 3 mA/cm{sup 2} after 2 h of electrodeposition time with the rotating cathode speed of 50 rpm. The cross sectional micro-indentation studies indicated that the Ru layer has hardness as high as 450 ± 10 HV.

ESR studies of electron irradiated K3Ir(CN)6 in KCl single crystals

International Nuclear Information System (INIS)

Vugman, N.V.; Pinhal, N.M.

1983-01-01

ESR studies of KCl single crystals doped with small amounts of K 3 Ir(CN) 6 and submitted to a prolongued 2 MeV electron irradiation at room temperature reveal the presence of the [IR(CN) 5 Cl] 4- and [Ir(CN) 4 Cl 2 ] 4- new molecular species. Ligand spin densities and ligand field parameters are calculated from the experimental hyperfine and superhyperfine interactions and compared to previous data on the [Ir(CN) 5 ] 4- species. (Author) [pt

Electroplating of erbium on steel surface in ErCl3 doped LiCl-KCl

International Nuclear Information System (INIS)

Kondo, Masatoshi; Tanaka, Teruya; Muroga, Takeo; Tsujimura, Hiroyuki; Ito, Yasuhiko

2012-01-01

The electroplating of Er metal on the reduced activation ferritic martensitic steel, JLF-1 (Fe-9Cr-2W-0.1C), in a molten salt was studied. The specimen was immersed in the molten ErCl 3 doped LiCl-KCl electrolyte. The electroplating was carried out by a constant potential electrolysis method and a pulsed current electrolysis method. It was found that the Er metal was deposited on the specimen surface due to the electrochemical reaction. (author)

Thermodiffusive behaviour of NaCl and KCl aqueous solutions a model for the Na-K pump

International Nuclear Information System (INIS)

Gaeta, F.S.; Mita, D.G.; Perna, G.; Scala, G.

1975-01-01

In NaCl and KCl aqueous nonisothermal solutions K + inverts its sense of migration within the physiological concentration range; Na + behaves similarly at much lower concentrations. These findings are discussed in relation to solute induced modifications of water structure and of their influence on thermal diffusion. A possible evolutionary model of a thermodiffusive mechanism for the sodium potassium pump is also suggested

Electrochemical Behavior of La on Liquid Bi electrode in LiCl-KCl molten salt

Energy Technology Data Exchange (ETDEWEB)

Kim, Beom Kyu; Han, Hwa Jeong; Park, Byung Gi [Soonchunyang University, Asan (Korea, Republic of)

2016-05-15

Pyroprocessing technology aims to achieve a grouped and efficiently separation of all actinide for recycling with a sufficient decontamination of fission products generating the minimum. The main steps of the pyroprocess is electrowinning process, where the remaining elements in a molten salt after electrorifinning process. That process is U, MAs are concurrently recovered at the liquid metal. Recently, a study of the liquid metal and molten salt using an electrochemical is carried out in a variety of fields. However, there is deficient information about the electrode reaction of lanthanide and actinide on the liquid bismuth metal electrodes. In this paper, the electrochemical behavior of La(III), with liquid bismuth was investigated by the electrochemical method. The aim of this study is to investigate the electrochemical behavior of lanthanum or neodymium among lanthanides in molten LiCl-KCl salt at liquid metal bismuth electrode cyclic voltammetry and derive the thermochemical properties. The electrochemical behavior of La was studied in LiCl-KCl-LaCl{sub 3} molten salts using electrochemical techniques Cyclic Voltammetry on liquid Bi electrodes at 773K. During the process of cyclic voltammetry electrolysis, intermetallic compound were observed of La, Lax-Biy, Li-Bi. The diffusion coefficient of La was measured by cyclic voltemmetry and was found to be 8.18x10{sup -5}cm{sup 2}/s.

The influence of oxide on the electrochemical processes in K2NbF7-NaCl-KCl melts

DEFF Research Database (Denmark)

Lantelme, F.; Berghoute, Y.; Barner, Jens H. Von

1995-01-01

Transient electrochemical techniques showed that in NaCl-KCl melts the reduction of K2NbF7 occurs through atwo-step reaction Nb(V) --> Nb(IV) --> Nb. When oxide ions were introduced, cyclic voltammetry indicated that the wavescorresponding to reduction of the complex NbF72- progressively...

Thermodynamics of HfCl4-KCl molten mixtures containing HfCl4 up to 33.3 mol. per cent

International Nuclear Information System (INIS)

Smirnov, M.V.; Salyulev, A.B.; Kudyakov, V.Ya.

1980-01-01

Based on measurements of saturated vapour pressure in components of melted mixtures of HfCl 4 -KCl, depending on temperature and concentration, calculated are the results of changes in activity coefficients of hafnium tetrachloride and potassium chloride on transition from diluted solutions, where the Henry law is met, to those concentrated where the law is disobeyed. Growth in the activity coefficient of HfCl 4 is due to dissociation of complex groups of HfCl 6 2- into complexes with a lesser number of ligands and decreasing relative binding energy of Hf 4+ -Cl - there. In this case, marked changes take place in partial enthalpy and entropy of hafnium tetrachloride mixing. Similar dependences are observed for potassium chloride, but they are expressed considerably weaker. Evaporation enthalpy and entropy are calculated for HfCl 4 and KCl monomers from their melted mixtures of various concentrations

Density of molten salt Mixtures of eutectic LiCl-KCl containing UCl{sub 3}, CeCl{sub 3}, or LaCl{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Zhang, C.; Simpson, M. F. [Dept. of Metallurgical Engineering, University of Utah, Salt Lake City (United States)

2017-06-15

Densities of molten salt mixtures of eutectic LiCl-KCl with UCl{sub 3}, CeCl{sub 3}, or LaCl{sub 3} at various concentrations (up to 13 wt%) were measured using a liquid surface displacement probe. Linear relationships between the mixture density and the concentration of the added salt were observed. For LaCl{sub 3} and CeCl{sub 3}, the measured densities were signifcantly higher than those previously reported from Archimedes’ method. In the case of LiCl-KCl-UCl{sub 3}, the data ft the ideal mixture density model very well. For the other salts, the measured densities exceeded the ideal model prediction by about 2%.

Diffusion of manganese ions in agar gel containing alkali metal chlorides

International Nuclear Information System (INIS)

Borhade, A.V.

2000-01-01

The obstruction effect for tracer-diffusion of Mn 2+ ions in the presence of different supporting electrolytes (LiCl, NaCl, KCl, CsCl) at various concentrations has been studied at 25 deg C using the zone diffusion technique. It has been observed that the obstruction effect determined in terms of α increases with concentration of the electrolyte. Further, for a given concentration it is found to decrease with increasing charge density of the cation. We also report here on the effect of temperature on obstruction and found that is constant over the temperature range studied (25-45 deg C). These observations are explained on the basis of competitive hydration between ions and agar macromolecules. (author)

Effect of oxide ion concentration on the electrochemical oxidation of carbon in molten LiCl

International Nuclear Information System (INIS)

Yun, J. W.; Choi, I. K.; Park, Y. S.; Kim, W. H.

2001-01-01

The continuous measurement of lithium oxide concentration was required in DOR (Direct Oxide Reduction) process, which converts spent nuclear fuel to metal form, for the reactivity monitor and effective control of the process. The concentration of lithium oxide was measured by the electrochemical method, which was based on the phenomenon that carbon atoms of glassy carbon electrode electrochemically react with oxygen ions of lithium oxide in molten LiCl medium. From the results of electrode polarization experiments, the trend of oxidation rate of carbon atoms was classified into two different regions, which were proportional and non-proportional ones, dependent on the amount of lithium oxide. Below about 2.5 wt % Li 2 O, as the carbon atom ionization rate was fast enough for reacting with diffusing lithium oxide to the surface of carbon electrode. In this concentration range, the oxidation rate of carbon atoms was controlled by the diffusion of lithium oxide, and the concentration of lithium oxide could be measured by electrochemical method. But, above 2.5 wt % Li 2 O, the oxidation rate of carbon atoms was controlled by the applied electrochemical potential, because the carbon atom ionization rate was suppressed by the huge amounts of diffusing Li 2 O. Above this concentration, the electrochemical method was not applicable to determine the concentration of lithium oxide

Partial molar volumes and viscosities of aqueous hippuric acid solutions containing LiCl and MnCl2 · 4H2O at 303.15 K

Science.gov (United States)

Deosarkar, S. D.; Tawde, P. D.; Zinjade, A. B.; Shaikh, A. I.

2015-09-01

Density (ρ) and viscosity (η) of aqueous hippuric acid (HA) solutions containing LiCl and MnCl2 · 4H2O have been studied at 303.15 K in order to understand volumetric and viscometric behavior of these systems. Apparent molar volume (φv) of salts were calculated from density data and fitted to Massons relation and partial molar volumes (φ{v/0}) at infinite dilution were determined. Relative viscosity data has been used to determine viscosity A and B coefficients using Jones-Dole relation. Partial molar volume and viscosity coefficients have been discussed in terms of ion-solvent interactions and overall structural fittings in solution.

Reduction behavior of UO22+ in molten LiCl–RbCl and LiCl–KCl eutectics by using tungsten

International Nuclear Information System (INIS)

Nagai, Takayuki; Uehara, Akihiro; Fujii, Toshiyuki; Yamana, Hajimu

2013-01-01

The reduction of uranium from UO 2 2+ to UO 2 + or U 4+ in molten LiCl–RbCl and LiCl–KCl eutectics was examined by using tungsten and chlorine gas. Spectrophotometric technique was adopted to determine the concentration of uranium species. When tungsten was immersed into the LiCl–RbCl eutectic melt at 400 °C without supplying chlorine gas, 36% of the total weight of the hexavalent of UO 2 2+ was reduced to the pentavalent of UO 2 + . Under purging chlorine gas into the melt, 96% of UO 2 2+ was reduced to the tetravalent of U 4+ . Tungsten oxy-chloride of WOCl 4 was produced via the reductions of UO 2 2+ , which was volatized from the melt and adsorbed on the upper part of experimental cell. On the other hand, 84% of UO 2 2+ in the LiCl–KCl eutectic melt at 500 °C was reduced to U 4+ by using tungsten and chlorine gas

Reduction behavior of UO22+ in molten LiCl-RbCl and LiCl-KCl eutectics by using tungsten

Science.gov (United States)

Nagai, Takayuki; Uehara, Akihiro; Fujii, Toshiyuki; Yamana, Hajimu

2013-08-01

The reduction of uranium from UO22+ to UO2+ or U4+ in molten LiCl-RbCl and LiCl-KCl eutectics was examined by using tungsten and chlorine gas. Spectrophotometric technique was adopted to determine the concentration of uranium species. When tungsten was immersed into the LiCl-RbCl eutectic melt at 400 °C without supplying chlorine gas, 36% of the total weight of the hexavalent of UO22+ was reduced to the pentavalent of UO2+. Under purging chlorine gas into the melt, 96% of UO22+ was reduced to the tetravalent of U4+. Tungsten oxy-chloride of WOCl4 was produced via the reductions of UO22+, which was volatized from the melt and adsorbed on the upper part of experimental cell. On the other hand, 84% of UO22+ in the LiCl-KCl eutectic melt at 500 °C was reduced to U4+ by using tungsten and chlorine gas.

Electrochemical investigation on the redox chemistry of niobium in LiCl-KCl-KF-Na2O melts

DEFF Research Database (Denmark)

Gillesberg, Bo; Bjerrum, Niels; Barner, Jens H. Von

1997-01-01

The system LiCl-KCl-KF-1 mole percent K2NbF7 (molar ration F-/Nb = 8) has been investigated in-the temperature range 370 to 725 degrees C by cyclic and square wave voltammetry. In the temperature range from 370 to 520 degrees C Nb(V) was reduced to Nb(III) in two reversible steps: Nb(V) --> Nb(IV...

Efeitos das fontes e níveis de sódio, cloro e potássio e da relação (Na + K/Cl, sobre o desempenho e características do plasma sangüíneo de poedeiras comerciais

Directory of Open Access Journals (Sweden)

Junqueira Otto Mack

2000-01-01

Full Text Available Dois experimentos foram realizados para estudar os efeitos da relação (Na + K/Cl na dieta de poedeiras comerciais no final do ciclo de postura, pela adição de bicarbonato de sódio (NaHCO3, cloreto de sódio (NaCl, cloreto de potássio (KCl e cloreto de amônia (NH4Cl, avaliando-se os parâmetros produtivos e características do plasma sangüíneo. O primeiro experimento envolveu cinco tratamentos: 0,30% de NaCl; 0,30% de NaCl + 0,95% de NaHCO3; 0,38% de KCl + 0,67% de NaHCO3; 0,38% de KCl + 1,62% de NaHCO3; e 0,38% de KCL + 2,56% de NaHCO3. A relação (Na + K/Cl foi, respectivamente, 3,46; 4,46; 4,46; 5,46; e 6,46. O segundo experimento envolveu quatro tratamentos: 0,30% NaCl; 0,47% de NaHCO3 + 0,19 de NH4Cl; 1,17% NaHCO3 + 0,19% de NH4Cl; e 1,88% de NaHCO3 + 0,19% de NH4Cl. A relação (Na + K/Cl foi 3,46; 4,46; 5,46; e 6,46, respectivamente. No primeiro experimento, o maior consumo alimentar foi observado nas aves alimentadas com dietas contendo 0,30% de NaCl. As aves que consumiram KCl apresentaram melhor conversão alimentar. Foi observado aumento no fósforo e pH do plasma sangüíneo. Aves que receberam dietas em que a relação (Na +K/Cl foi de 5,46 apresentaram maiores níveis de fósforo no plasma sangüíneo. O aumento do pH no plasma sangüíneo foi observado em aves que receberam dietas com relações de (Na + K/Cl de 4,46 e 6,46. No segundo experimento, o peso do ovo diminuiu com o aumento do NaHCO3 da dieta.

Zirconium behaviour during electrorefining of actinide-zirconium alloy in molten LiCl-KCl on aluminium cathodes

Energy Technology Data Exchange (ETDEWEB)

Meier, R. [European Commission, Joint Research Centre (JRC), Institute for Transuranium Elements (ITU), Postfach 2340, Karlsruhe 76125 (Germany); Heidelberg University, Institute of Physical Chemistry, Im Neuenheimer Feld 253, Heidelberg 69120 (Germany); Souček, P., E-mail: Pavel.Soucek@ec.europa.eu [European Commission, Joint Research Centre (JRC), Institute for Transuranium Elements (ITU), Postfach 2340, Karlsruhe 76125 (Germany); Malmbeck, R.; Krachler, M.; Rodrigues, A.; Claux, B.; Glatz, J.-P. [European Commission, Joint Research Centre (JRC), Institute for Transuranium Elements (ITU), Postfach 2340, Karlsruhe 76125 (Germany); Fanghänel, Th. [European Commission, Joint Research Centre (JRC), Institute for Transuranium Elements (ITU), Postfach 2340, Karlsruhe 76125 (Germany); Heidelberg University, Institute of Physical Chemistry, Im Neuenheimer Feld 253, Heidelberg 69120 (Germany)

2016-04-15

A pyrochemical electrorefining process for the recovery of actinides from metallic nuclear fuel based on actinide-zirconium alloys (An–Zr) in a molten salt is being investigated. In this process actinides are group-selectively recovered on solid aluminium cathodes as An–Al alloys using a LiCl–KCl eutectic melt at a temperature of 450 °C. In the present study the electrochemical behaviour of zirconium during electrorefining was investigated. The maximum amount of actinides that can be oxidised without anodic co-dissolution of zirconium was determined at a selected constant cathodic current density. The experiment consisted of three steps to assess the different stages of the electrorefining process, each of which employing a fresh aluminium cathode. The results indicate that almost a complete dissolution of the actinides without co-dissolution of zirconium is possible under the applied experimental conditions. - Highlights: • Recovery of actinides was shown by electrorefining of U/Pu–Zr alloys in LiCl–KCl. • Constant current density of 20 mA/cm{sup 2} is applied. • Most of the actinides were dissolved avoiding zirconium co-dissolution. • Deterioration of the deposit quality by a small amount of co-deposited Zr is not observed.

Lack of effect of nitric oxide on KCl, acetylcholine and substance P induced contractions in ileal longitudinal muscle of the rat.

Science.gov (United States)

Tanovic, A; Jiménez, M; Fernández, E

2000-06-23

The aim of this study was to determine whether an excess of nitric oxide (NO) (mimicked by addition of NO donors) might produce by itself changes in the contractile responses to acetylcholine (ACh), substance P (SP) and KCl in the longitudinal muscle of the rat ileum. We also studied the calcium handling properties of this tissue in presence of NO donors. The NO donors assayed sodium nitroprusside (SNP) and 3-morpholinosydnonimine hydrochloride (SIN-1), induced different responses. SNP caused an immediate contraction followed by a sustained relaxation, whereas SIN-1 induced an immediate relaxation followed by a contraction. Even after prolonged incubations (up to 90 min), the NO donors SNP and SIN-1 were unable to modify the ACh- and SP-concentration-response curves, as well as the response to 30 mM KCl. The nifedipine-resistant component of the ACh-induced contraction was not modified in presence of SNP. Cyclopiazonic acid (CPA) induced a contraction that was not modified when the tissue was pre-incubated with SNP. Nifedipine caused a sharp relaxation when added during the CPA-induced contraction and, when added previously, it reduced the CPA-induced contractile response. It is concluded that NO excess is not, by itself, responsible for the altered responses to KCl. ACh and SP. The contractility changes observed in the longitudinal muscle of the rat ileum during inflammation could rather be related to the presence of other inflammatory mediators.

Laser Clad and HVOF-Sprayed Stellite 6 Coating in Chlorine-Rich Environment with KCl at 700 °C.

Czech Academy of Sciences Publication Activity Database

Pala, Z.; Bai, M.; Lukáč, František; Hussain, T.

2017-01-01

Roč. 88, 5-6 (2017), s. 749-771 ISSN 0030-770X Institutional support: RVO:61389021 Keywords : Stellite 6 * KCl * High-temperature corrosion * HVOF * Laser cladding Subject RIV: JK - Corrosion ; Surface Treatment of Materials OBOR OECD: Coating and films Impact factor: 1.196, year: 2016 https://link.springer.com/article/10.1007/s11085-017-9776-7

Pyrochemical extraction for selective removal of transuranium elements from molten LiCl-KCl

International Nuclear Information System (INIS)

Ackermann, J.P.; Johnson, T.R.

1993-01-01

Recent determinations of separation factors that describe partition of the actinide and rare earth elements between liquid cadmium and LiCl-KCl eutectic allowed identification of a process for selective removal of the transuranium (TRU) element chlorides from the electrolyte used for electrofining of metal fuel from the Integral Fast Reactor. It is periodically necessary to remove rare earth elements from the electrolyte to limit heat generation from radioactive decay. Countercurrent extraction of electrolyte with uranium in cadmium solution allows retention of valuable TRU elements in the reprocessed fuel, and results in a rare earth waste stream that is essentially free of TRU elements and their concomitant long-term hazards

Translational energy of products in the K+CH3COCl --> KCl+CH3CO reaction

Science.gov (United States)

Pauluth, M.; Rotzoll, G.

1984-08-01

Time-of-flight distributions of product KCl from the K+CH3COCl reaction have been measured over limited angular ranges at the collision energies 0.16 and 0.70 eV (cm). A simplified analysis assuming separability of cm angle and velocity yields the products' mean translational energy Ē'T. ĒT is very low for the lower collision energy, but increases with increasing collision energy. This finding is in accord with the photodissociation model of Herschbach, that predicts low repulsive energy release for this system.

Characterization of an extracellular epitope antibody to the neuronal K-Cl cotransporter, KCC2.

Science.gov (United States)

Gagnon, Kenneth Be; Fyffe, Robert Ew; Adragna, Norma C; Lauf, Peter K

2007-07-01

1. Ion gradients across the cell membrane are important for proper cellular communication and homeostasis. With the exception of erythrocytes, chloride (Cl), one of the most important free anions in animal cells, is not distributed at thermodynamic equilibrium across the plasma membrane. The K-Cl cotransporter (COT), consisting of at least four isoforms, utilizes the larger outwardly directed chemical driving force of K to expel Cl from the cell against its inwardly directed chemical gradient and has been implicated recently as one of the main Cl extruders in developing neurons. 2. Previous in situ hybridization studies have indicated widespread mRNA distribution of the neuronal-specific K-Cl COT isoform (KCC2) throughout the rat central nervous system (CNS). However, immunohistochemical studies have been limited owing to the availability of a more selective antibody to KCC2. The goal of the present study was to develop a new molecular tool for the immunohistochemical identification and neuronal distribution of KCC2. 3. Herein, we present evidence of immunohistochemical corroboration of the widespread KCC2 mRNA expression using a novel extracellular anti-peptide antibody directed against the second extracellular loop (ECL2) of KCC2. Immunoperoxidase and immunofluorescent labelling revealed widespread post-synaptic somatic and dendritic localization of KCC2 in multiple neuronal populations in the cerebral cortex, hippocampus, brainstem, lumbar spinal cord and cerebellum. We also demonstrate that binding of the antibody to an extracellular epitope within ECL2 does not alter cotransporter function. In essence, the present study reports on a new molecular tool for structural and functional studies of KCC2.

An experimental study of the solubility of molybdenum in H₂O and KCl-H₂O solutions from 500 ºC to 800 ºC, and 150 to 300 MPa

Energy Technology Data Exchange (ETDEWEB)

Ulrich, Thomas; Mavrogenes, John [Australian National University

2008-04-22

The solubility of molybdenum (Mo) was determined at temperatures from 500 °C to 800 °C and 150 to 300 MPa in KCl-H₂O and pure H₂O solutions in cold-seal experiments. The solutions were trapped as synthetic fluid inclusions in quartz at experimental conditions, and analyzed by laser ablation inductively coupled plasma mass spectrometry (LA ICPMS). Mo solubilities of 1.6 wt% in the case of KCl-bearing aqueous solutions and up to 0.8 wt% in pure H₂O were found. Mo solubility is temperature dependent, but not pressure dependent over the investigated range, and correlates positively with salinity (KCl concentration). Molar ratios of ~1 for Mo/Cl and Mo/K are derived based on our data. In combination with results of synchrotron X-ray absorption spectroscopy of individual fluid inclusions, it is suggested that Mo-oxo-chloride complexes are present at high salinity (>20 wt% KCl) and ion pairs at moderate to low salinity (<11 wt% KCl) in KCl-H₂O aqueous solutions. Similarly, in the pure H₂O experiments molybdic acid is the dominant species in aqueous solution. The results of these hydrothermal Mo experiments fit with earlier studies conducted at lower temperatures and indicate that high Mo concentrations can be transported in aqueous solutions. Therefore, the Mo concentration in aqueous fluids seems not to be the limiting factor for ore formation, whereas precipitation processes and the availability of sulfur appear to be the main controlling factors in the formation of molybdenite (MoS₂).

Thermodynamics of HfCl/sub 4/-KCl molten mixtures containing HfCl/sub 4/ up to 33. 3 mol. per cent

Energy Technology Data Exchange (ETDEWEB)

Smirnov, M V; Salyulev, A B; Kudyakov, V Ya [AN SSSR, Sverdlovsk. Inst. Ehlektrokhimii

1980-05-01

Based on measurements of saturated vapour pressure in components of melted mixtures of HfCl/sub 4/-KCl, depending on temperature and concentration, calculated are the results of changes in activity coefficients of hafnium tetrachloride and potassium chloride on transition from diluted solutions, where the Henry law is met, to those concentrated where the law is disobeyed. Growth in the activity coefficient of HfCl/sub 4/ is due to dissociation of complex groups of HfCl/sub 6//sup 2 -/ into complexes with a lesser number of ligands and decreasing relative binding energy of Hf/sup 4 +/-Cl/sup -/ there. In this case, marked changes take place in partial enthalpy and entropy of hafnium tetrachloride mixing. Similar dependences are observed for potassium chloride, but they are expressed considerably weaker. Evaporation enthalpy and entropy are calculated for HfCl/sub 4/ and KCl monomers from their melted mixtures of various concentrations.

Thermoluminiscence and thermal annealing of F centres in KCL gamma irradiated

International Nuclear Information System (INIS)

Ausin Alonso, Vicente.

1976-01-01

The thermoluminiscence spectrum and phosphorescence decays of Harshaw KCl samples gamma irradiated at room temperature have been studied up to 400 0 C. For the six peaks found, the order of recombination kinetics, the pre-exponential factor and the activation energy have been obtained. It has been observed that the area under the thermoluminiscence curve is always proportional to the F centre concentration in the sample before heating. It was also found that there is an annealing step of F centres corresponding to each thermoluminiscence peak, when the temperature of the sample is raised at a constant rate. It is concluded that the F centres play the role of recombination centres in the annealing process, the interstitials being the mobile entities moving towards there combination centre. At some stage in the process light is emitted. (author)

Behavior in the open field predicts the number of KCl-induced cortical spreading depressions in rats.

Science.gov (United States)

Bogdanov, Volodymyr Borysovych; Bogdanova, Olena Viktorivna; Koulchitsky, Stanislav Vladimirovich; Chauvel, Virginie; Multon, Sylvie; Makarchuk, Mykola Yukhymovych; Brennan, Kevin Christopher; Renshaw, Perry Franklin; Schoenen, Jean

2013-01-01

Anxiety disorders are known to be comorbid with migraine, and cortical spreading depression (CSD) is the most likely cause of the migraine aura. To search for possible correlations between susceptibility to CSD and anxiety we used the open field test in male Sprague-Dawley rats chronically treated with the preventive anti-migraine drugs valproate or riboflavin. Animals avoiding the central area of the open field chamber and those with less exploratory activity (i.e. rearing) were considered more anxious. After 4 weeks of treatment CSDs were elicited by application of 1M KCl over the occipital cortex and the number of CSDs occurring over a 2h period was compared to the previously assessed open field behavior. Higher anxiety-like behavior was significantly correlated with a higher frequency of KCl-induced CSDs. In saline-treated animals, fewer rearings were found in animals with more frequent CSDs (R=-1.00). The duration of ambulatory episodes in the open field center correlated negatively with number of CSDs in the valproate group (R=-0.83; popen field center in both groups (R=-0.75; p<0.05 and R=-0.58; p<0.1 respectively). These results suggest that anxiety symptoms are associated with susceptibility to CSD and might explain why it can be an aggravating factor in migraine with aura. Copyright © 2012 Elsevier B.V. All rights reserved.

Comparison of gaseous oxidized Hg measured by KCl-coated denuders, and nylon and cation exchange membranes.

Science.gov (United States)

Huang, Jiaoyan; Miller, Matthieu B; Weiss-Penzias, Peter; Gustin, Mae Sexauer

2013-07-02

The chemical compounds that make up gaseous oxidized mercury (GOM) in the atmosphere, and the reactions responsible for their formation, are not well understood. The limitations and uncertainties associated with the current method applied to measure these compounds, the KCl-coated denuder, are not known due to lack of calibration and testing. This study systematically compared the uptake of specific GOM compounds by KCl-coated denuders with that collected using nylon and cation exchange membranes in the laboratory and field. In addition, a new method for identifying different GOM compounds using thermal desorption is presented. Different GOM compounds (HgCl2, HgBr2, and HgO) were found to have different affinities for the denuder surface and the denuder underestimated each of these compounds. Membranes measured 1.3 to 3.7 times higher GOM than denuders in laboratory and field experiments. Cation exchange membranes had the highest collection efficiency. Thermodesorption profiles for the release of GOM compounds from the nylon membrane were different for HgO versus HgBr2 and HgCl2. Application of the new field method for collection and identification of GOM compounds demonstrated these vary as a function of location and time of year. Understanding the chemistry of GOM across space and time has important implications for those developing policy regarding this environmental contaminant.

Composition dependence of glow peak temperature in KCl1-xBrx doped with divalent cations

International Nuclear Information System (INIS)

Perez-Salas, R; Aceves, R; RodrIguez-Mijangos, R; Riveros, H G; Duarte, C

2004-01-01

Thermoluminescence measurements of β-irradiated Eu 2+ - and Ca 2+ - doped KCl 1-x KBr x solid solutions excited at room temperature have been carried out to identify the effect of composition on the glow peaks. A typical glow peak has been distinguished for each composition. A linear dependence of its temperature on the composition x has been found. These results indicate that for divalent impurity-doped alkali halide solid solutions these glow peak temperatures are mostly dependent on the lattice constant of the host than on the size of the anion or impurity cation

Effect of γ-irradiation on the lattice parameter and colour centre concentration in pure Ca2+, Sr2+ and Eu2+ doped KCl crystals

International Nuclear Information System (INIS)

Damm, J.Z.; Stepien-Damm, J.

1980-01-01

The changes of lattice parameter and colour centre concentration are examined in KCl crystals (both pure and Me 2+ -doped) irradiated by γ-rays at room temperature. For the pure crystals the relative volume change vs. F-centre concentration plot reveals the presence of two stages, one ascribed to the introduction of colour centre pairs (or F centres only) and other to the generation of new dislocations (or new dislocations with trapped-hole centres). In Me 2+ doped crystals the lattice expansion bears a complex character (in the initial irradiation stage a transient maximum appears). Additional anomaly appears in Eu 2+ KCl in the high-dose range where in spite of a distinct F-centre concentration drop a marked raise of the lattice parameter is observed. (author)

An upper limit on hypertriton production in collisions of Ar(1.76 A GeV) + KCl

International Nuclear Information System (INIS)

Agakishiev, G.; Chernenko, S.; Fateev, O.; Zanevsky, Y.; Belver, D.; Cabanelas, P.; Castro, E.; Garzon, J.A.; Blanco, A.; Fonte, P.; Lopes, L.; Mangiarotti, A.; Boehmer, M.; Friese, J.; Gernhaeuser, R.; Jurkovic, M.; Kruecken, R.; Maier, L.; Weber, M.; Boyard, J.L.; Hennino, T.; Liu, T.; Moriniere, E.; Ramstein, B.; Destefanis, M.; Gilardi, C.; Kuehn, W.; Lange, J.S.; Metag, V.; Spruck, B.; Dohrmann, F.; Kaempfer, B.; Kotte, R.; Naumann, L.; Wendisch, C.; Wuestenfeld, J.; Dybczak, A.; Michalska, B.; Palka, M.; Przygoda, W.; Salabura, P.; Trebacz, R.; Wisniowski, M.; Epple, E.; Fabbietti, L.; Lapidus, K.; Siebenson, J.; Finocchiaro, P.; Schmah, A.; Spataro, S.; Froehlich, I.; Lorenz, M.; Markert, J.; Michel, J.; Muentz, C.; Pachmayer, Y.C.; Pechenova, O.; Rehnisch, L.; Rustamov, A.; Scheib, T.; Schuldes, H.; Stroebele, H.; Tarantola, A.; Teilab, K.; Galatyuk, T.; Gonzalez-Diaz, D.; Golubeva, M.; Guber, F.; Ivashkin, A.; Karavicheva, T.; Kurepin, A.; Reshetin, A.; Sadovsky, A.; Gumberidze, M.; Heinz, T.; Holzmann, R.; Koenig, I.; Koenig, W.; Kolb, B.W.; Lang, S.; Pechenov, V.; Pietraszko, J.; Schwab, E.; Sturm, C.; Traxler, M.; Yurevich, S.; Iori, I.; Krasa, A.; Krizek, F.; Kugler, A.; Sobolev, Yu.G.; Tlusty, P.; Wagner, V.; Kuc, H.; Mousa, J.; Tsertos, H.; Stroth, J.

2013-01-01

A high-statistic data sample of Ar(1.76 AGeV)+KCl events recorded with HADES is used to search for a hypertriton signal. An upper production limit per centrality-triggered event of 1.04 x 10 -3 on the 3 σ level is derived. Comparing this value with the number of successfully reconstructed Λ hyperons allows to determine an upper limit on the ratio N 3 Λ H /N Λ , which is confronted with statistical and coalescence-type model calculations. (orig.)

The localized vibrations of H-H-, D-D- and H-D- pairs in KCl, KBr, KI, RbCl and NaCl

International Nuclear Information System (INIS)

Robert, R.

1974-01-01

The localized vibrational modes of H - H - , D - D - and H - D - pairs in KCl, KBr, KI, RbCl and NaCl were studied for different pair configurations. The measured frequencies of the infrared active modes were found to be in good agreement with a model of two coupled harmonic oscillators. The line width for different modes in the salts studied is discussed. The temperature dependence for the transversal modes T 1 and T 2 of the line width for the H - H - pairs in KCl indicates that the broadening of these lines is due to the 'decomposition mechanism', that generates two phonons. The generated phonons due to the decay of the localized in phase mode are: -one acustic phonon of the lattice, -one localized phonon that corresponds to the out of phase vibration of the H - H - pair. The general properties, as the Ivey law and several particulars of the properties in the alkali-halides studied are presented [pt

Temperature dependence of volume thermal expansion for NaCl and KCl crystals

International Nuclear Information System (INIS)

Fang Zhenghua

2005-01-01

A new relation for predicting volume thermal expansion of alkali halides at high temperatures is derived based on the assumption that the two different diffusional driving force models presented, respectively, by Sharma and Sharma (Indian J. Pure Appl. Phys. 29 (1991) 637) and Singh (J. Phys. Chem. Solids 63 (2002) 1935) are equivalent. The input parameters needed for the calculation are the volume thermal expansion coefficient and the isothermal Anderson-Gruneisen parameter, both at room temperature and zero pressure, which are available from the literature. The tests on NaCl and KCl crystals demonstrate that the agreement between the calculated results obtained by this relation and the corresponding experimental data is very good. The applicability of the relation as well as some thermodynamic relationships included in its derivation is discussed

Thermodynamic properties of (LiCl + N,N-dimethylacetamide) and (LiBr + N,N-dimethylacetamide) at temperatures from (323.15 to 423.15) K

International Nuclear Information System (INIS)

Nasirzadeh, Karamat; Neueder, Roland; Kunz, Werner

2005-01-01

Precise vapor pressure data for LiCl and LiBr solutions in N,N-dimethylacetamide are given for T = (323.15 to 423.15) K. The molality ranges covered in this study are about m = (0.073 to 1.89) mol . kg -1 for lithium chloride and m = (0.06 to 1.75) mol . kg -1 for lithium bromide. Osmotic coefficients are calculated by taking into account the second virial coefficient of N,N-dimethylacetamide. The parameters of the extended Pitzer-ion interaction model of Archer, of the MSA-NRTL model and of the chemical model of Barthel are evaluated. These models accurately reproduce the experimental osmotic coefficients within different concentration ranges. The parameters of the Pitzer-ion interaction model of Archer are used to calculate the mean molal activity coefficients and excess Gibbs free energies. The non-ideal behaviors of these systems are discussed in terms of the model parameters

An upper limit on hypertriton production in collisions of Ar(1.76 A GeV) + KCl

Energy Technology Data Exchange (ETDEWEB)

Agakishiev, G.; Chernenko, S.; Fateev, O.; Zanevsky, Y. [Joint Institute of Nuclear Research, Dubna (Russian Federation); Belver, D.; Cabanelas, P.; Castro, E.; Garzon, J.A. [Univ. de Santiago de Compostela, LabCAF. F. Fisica, Santiago de Compostela (Spain); Blanco, A.; Fonte, P.; Lopes, L.; Mangiarotti, A. [LIP-Laboratorio de Instrumentacao e Fisica Experimental de Particulas, Coimbra (Portugal); Boehmer, M.; Friese, J.; Gernhaeuser, R.; Jurkovic, M.; Kruecken, R.; Maier, L.; Weber, M. [Technische Universitaet Muenchen, Physik Department E12, Garching (Germany); Boyard, J.L.; Hennino, T.; Liu, T.; Moriniere, E.; Ramstein, B. [Universite Paris Sud, Institut de Physique Nucleaire (UMR 8608), CNRS/IN2P3, Orsay Cedex (France); Destefanis, M.; Gilardi, C.; Kuehn, W.; Lange, J.S.; Metag, V.; Spruck, B. [Justus Liebig Universitaet Giessen, II. Physikalisches Institut, Giessen (Germany); Dohrmann, F.; Kaempfer, B.; Kotte, R.; Naumann, L.; Wendisch, C.; Wuestenfeld, J. [Helmholtz-Zentrum Dresden-Rossendorf, Institut fuer Strahlenphysik, Dresden (Germany); Dybczak, A.; Michalska, B.; Palka, M.; Przygoda, W.; Salabura, P.; Trebacz, R.; Wisniowski, M. [Jagiellonian University of Cracow, Smoluchowski Institute of Physics, Krakow (Poland); Epple, E.; Fabbietti, L.; Lapidus, K.; Siebenson, J. [Excellence Cluster ' ' Origin and Structure of the Universe' ' , Garching (Germany); Finocchiaro, P.; Schmah, A.; Spataro, S. [Laboratori Nazionali del Sud, Istituto Nazionale di Fisica Nucleare, Catania (Italy); Froehlich, I.; Lorenz, M.; Markert, J.; Michel, J.; Muentz, C.; Pachmayer, Y.C.; Pechenova, O.; Rehnisch, L.; Rustamov, A.; Scheib, T.; Schuldes, H.; Stroebele, H.; Tarantola, A.; Teilab, K. [Goethe-Universitaet, Institut fuer Kernphysik, Frankfurt (Germany); Galatyuk, T.; Gonzalez-Diaz, D. [Technische Universitaet Darmstadt, Darmstadt (Germany); Golubeva, M.; Guber, F.; Ivashkin, A.; Karavicheva, T.; Kurepin, A.; Reshetin, A.; Sadovsky, A. [Russian Academy of Science, Institute for Nuclear Research, Moscow (Russian Federation); Gumberidze, M. [Technische Universitaet Darmstadt, Darmstadt (Germany); Universite Paris Sud, Institut de Physique Nucleaire (UMR 8608), CNRS/IN2P3, Orsay Cedex (France); Heinz, T.; Holzmann, R.; Koenig, I.; Koenig, W.; Kolb, B.W.; Lang, S.; Pechenov, V.; Pietraszko, J.; Schwab, E.; Sturm, C.; Traxler, M.; Yurevich, S. [GSI Helmholtzzentrum fuer Schwerionenforschung GmbH, Darmstadt (Germany); Iori, I. [Istituto Nazionale di Fisica Nucleare, Sezione di Milano, Milano (Italy); Krasa, A.; Krizek, F.; Kugler, A.; Sobolev, Yu.G.; Tlusty, P.; Wagner, V. [Academy of Sciences of Czech Republic, Nuclear Physics Institute, Rez (Czech Republic); Kuc, H. [Jagiellonian University of Cracow, Smoluchowski Institute of Physics, Krakow (Poland); Universite Paris Sud, Institut de Physique Nucleaire (UMR 8608), CNRS/IN2P3, Orsay Cedex (France); Mousa, J.; Tsertos, H. [University of Cyprus, Department of Physics, Nicosia (Cyprus); Stroth, J. [GSI Helmholtzzentrum fuer Schwerionenforschung GmbH, Darmstadt (Germany); Goethe-Universitaet, Institut fuer Kernphysik, Frankfurt (Germany); Collaboration: HADES Collaboration

2013-11-15

A high-statistic data sample of Ar(1.76 AGeV)+KCl events recorded with HADES is used to search for a hypertriton signal. An upper production limit per centrality-triggered event of 1.04 x 10{sup -3} on the 3 {sigma} level is derived. Comparing this value with the number of successfully reconstructed {Lambda} hyperons allows to determine an upper limit on the ratio N{sub 3{sub {Lambda}H}}/N{sub {Lambda}}, which is confronted with statistical and coalescence-type model calculations. (orig.)

Electrodeposition of Al-Ta alloys in NaCl-KCl-AlCl{sub 3} molten salt containing TaCl{sub 5}

Energy Technology Data Exchange (ETDEWEB)

Sato, Kazuki; Matsushima, Hisayoshi; Ueda, Mikito, E-mail: mikito@eng.hokudai.ac.jp

2016-12-01

Highlights: • Electrodeposition of Al-Ta alloys in an AlCl{sub 3}-NaCl-KCl-TaCl{sub 5} melt was carried out. • We were obtained 72 at% Ta-Al alloy at 0.3 V. • Amorphous Ta-Al was formed in high Ta concentration. - Abstract: To form Al-Ta alloys for high temperature oxidation resistance components, molten salt electrolysis was carried out in an AlCl{sub 3}-NaCl-KCl melt containing TaCl{sub 5} at 423 K. The voltammogram showed two cathodic waves at 0.45 V and 0.7 V vs. Al/Al(III), which may correspond to reduction from Ta(V) to Ta(III) and from Ta(III) to tantalum metal, respectively. Electrodeposits of Al and Ta were obtained in the range from −0.05 to 0.3 V and the highest concentration of Ta in the electrodeposit was 72 at% at 0.3 V. With increasing Ta content in the alloy, the morphology of the electrodeposits became powdery and the particle size smaller.

Generation of KCL035 research grade human embryonic stem cell line carrying a mutation in HBB gene

Directory of Open Access Journals (Sweden)

Heema Hewitson

2016-03-01

Full Text Available The KCL035 human embryonic stem cell line was derived from an embryo donated for research that carried a mutation in the HBB gene, which is linked to the β-thalassemia syndrome. The ICM was isolated using laser microsurgery and plated on γ-irradiated human foreskin fibroblasts. Both the derivation and cell line propagation were performed in an animal product-free environment. Pluripotent state and differentiation potential were confirmed by in vitro assays.

INTERACTION OF LASER RADIATION WITH MATTER: Influence of Ca and Pb impurities on the bulk optical strength of ultrapure NaCl and KCl crystals

Science.gov (United States)

Vinogradov, An V.; Voszka, R.; Kovalev, Valerii I.; Faĭzullov, F. S.; Janszky, J.

1987-06-01

A significant increase (by a factor of about 3) of the bulk damage threshold in the case of interaction of CO2 laser radiation pulses with ultrapure NaCl and KCl crystals grown in a reactive atmosphere was observed on introduction of divalent metal ions Ca and Pb in concentrations of 10-5-10-6 mol/mol. Impurities were introduced in concentrations of 10-8-10-3 and 2×10-7-10-4 mol/mol into the melts of KCl and NaCl, respectively. The concentration of other impurities (including OH) did not exceed ~10-6 mol/mol. A physical model was developed to account for the observed dependence on the basis of an analogy between a system of colloidal particles and F centers in a crystal and a liquid-vapor system.

Fluorescence Resonance Energy Transfer of the Tb(III)-Nd(III) Binary System in Molten LiCl-KCl Eutectic Salt

Energy Technology Data Exchange (ETDEWEB)

Kim, B. Y. [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of); Yun, J. I. [KAIST, Daejeon (Korea, Republic of)

2015-05-15

The lanthanides act as a neutron poison in nuclear reactor with large neutron absorption cross section. For that reason, very low amount of lanthanides is required in the recovered U/TRU ingot product from pyrochemical process. In view of that, the investigation of thermodynamic properties and chemical behaviors of lanthanides in molten chloride salt are necessary to estimate the performance efficiency of pyrochemical process. However, there are uncertainties about knowledge and understanding of basic mechanisms in pyrochemical process, such as chemical speciation and redox behaviors due to the lack of in-situ monitoring methods for high temperature molten salt. The spectroscopic analysis is one of the probable techniques for in-situ qualitative and quantitative analysis. Recently, a few fluorescence spectroscopic measurements on single lanthanide element in molten LiCl-KCl eutectic have been investigated. The fluorescence intensity and the fluorescence lifetime of Tb(III) were decreased as increasing the concentration of Nd(III), demonstrating collisional quenching between donor ions and acceptor ions. The Forster distance (..0) of Tb(III)-Nd(III) binary system in molten LiCl-KCl eutectic was determined in the specific range of .... (0.1-1.0) and .. (1.387-1.496)

Chrono-potentiometry in molten chlorides. Application to the study of the electrochemical properties of uranium and plutonium in the LiCl-KCl eutectic; Chronopotentiometrie dans les chlorures fondus. Application a l'etude des proprietes electrochimiques de l'uranium et du plutonium dans l'eutectique LiCl-KCl

Energy Technology Data Exchange (ETDEWEB)

Leseur, A. [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

1969-05-01

Using solutions of cadmium chloride in the eutectic LiCl-KCl, a chrono-potentiometric method has been developed with a view to its application to the study of molten solutions. Particular attention has been paid to the choice of the indicator electrodes. The method makes it possible to analyze molten solutions quantitatively and to determine diffusion coefficients and their activation energies; it yields furthermore information about the nature and the behaviour of ionic species in solution. The method has been applied to the study of solutions of uranium and plutonium chloride in the eutectic LiCl-KCl. Linear chrono-amperometry has been used for studying these solutions quantitatively, but chrono-potentiometry, of which the theory is better developed, is better suited to a quantitative study. The results obtained have made it possible to determine the diffusion coefficients of the ions Cd{sup 2+}, U{sup 3+}, U{sup 4+} and U(IV) in the presence of F{sup -} and Pu{sup 3+} ions, as well as the activation energy of the diffusion coefficients. (author) [French] La mise au point de la chronopotentiometrie comme moyen d'etude des solutions fondues a ete effectuee avec des solutions de chlorure de cadmium dans l'eutectique LiCl-KCl. Le probleme du choix des electrodes indicatrices a ete particulierement etudie. La methode permet l'analyse quantitative des solutions fondues ainsi que la determination des coefficients de diffusion et de leurs energies d'activation: elle donne en outre des renseignements sur la nature et le comportement des especes ioniques en solution. Elle a ete appliquee a l'etude des solutions des chlorures d'uranium et de plutonium dans l'eutectique LiCl-KCl. La chronoamperometrie lineaire a ete utilisee pour l'etude qualitative de ces solutions, mais la chronopotentiometrie, dont la theorie est plus complete, convient mieux pour l'etude quantitative. Les resultats obtenus ont permis de determiner les

Separation of lanthanum from samarium on solid aluminum electrode in LiCl-KCl eutectic melts

International Nuclear Information System (INIS)

De-Bin Ji; Mi-Lin Zhang; Xing Li; Xiao-Yan Jing; Wei Han; Yong-De Yan; Yun Xue; Zhi-Jian Zhang; Harbin Engineering University, Harbin

2015-01-01

This paper presents an electrochemical study on the separation of lanthanum from samarium on aluminum electrode at 773 K. The results from different electrochemical methods showed that Sm(III) and La(III) formed Al-Sm and Al-La intermetallic compounds on an aluminum electrode at electrode potential around -1.67 and -1.46 V, respectively. The electrochemical separation of lanthanum was carried out in LiCl-KCl-LaCl 3 -SmCl 3 melts on solid aluminum electrodes at 773 K by potentiostatic electrolysis at -1.45 V for 40 h and the separation efficiency was 99.1 %. (author)

Spectroscopy of virtual photons in Ar+KCl collisions at Ekin=1.76 AGeV

International Nuclear Information System (INIS)

Jurkovic, Martin

2010-01-01

The objective of this thesis is the analysis of virtual photon emission originating from the decays of the short lived hadrons produced in Ar+KCl collisions at E kin =1.76 AGeV. The measured observables were the reconstructed e + e - pairs and their kinematic distributions. The data were recorded with the HADES spectrometer assembled at GSI Helmholtzzentrum fuer Schwerionenforschung GmbH in Darmstadt, Germany. Due to the considerably higher combinatorial background originating from the γ-conversion as compared to that from light collision systems (p+p,C+C) investigated so far with HADES, a new method for identification and suppression of conversion electrons using the signal pattern in the RICH-detector was studied. An improvement of signal to background ratio (S/B) reaching 30% was achieved. For the procedure of calculating the e + /e - track efficiencies a detailed study of RICH detector signals was performed, leading to an overall improved description of ring observables in the simulation. In total, 32545pm 385 e + e - signal pairs with an opening angle α ee > 15 and 0.1 e ee 2 ) and 253±25 for masses M ee > 0.55 GeV/c 2 . A clear signal from direct ω decay with S/B ∝1 was identified for the first time in the SIS18 energy regime. The extraction of the ω yield per produced π 0 results in N(ω)/N(π 0 ) ∼ (4,5 ± 2,5(stat) ± 2(sys)) .10 -8 . The e + e - production in the η mass region was compared to the expected η Dalitz decay η→γe + e - contribution. The measured e + e - yield is higher by a factor F = 3.4±0.2(stat)±0.6(sys)±0.9(η) as compared to the η production. The excitation function of the extra e + /e - sources shows similar energy dependence as the π 0 production. Possible candidates for these extra e + e - sources are the Δ Dalitz decays, the NN and πN bremsstrahlung and partly the direct decay of the ρ meson. Relative to the π 0 production in both Ar+KCl and C+C collisions, the e + e - production of unknown composition in Ar+KCl

Spectroscopy of virtual photons in Ar+KCl collisions at E{sub kin}=1.76 AGeV; Spektroskopie virtueller Photonen in Ar+KCl Stoessen bei E{sub kin}=1,76 AGeV

Energy Technology Data Exchange (ETDEWEB)

Jurkovic, Martin

2010-01-14

The objective of this thesis is the analysis of virtual photon emission originating from the decays of the short lived hadrons produced in Ar+KCl collisions at E{sub kin}=1.76 AGeV. The measured observables were the reconstructed e{sup +}e{sup -} pairs and their kinematic distributions. The data were recorded with the HADES spectrometer assembled at GSI Helmholtzzentrum fuer Schwerionenforschung GmbH in Darmstadt, Germany. Due to the considerably higher combinatorial background originating from the {gamma}-conversion as compared to that from light collision systems (p+p,C+C) investigated so far with HADES, a new method for identification and suppression of conversion electrons using the signal pattern in the RICH-detector was studied. An improvement of signal to background ratio (S/B) reaching 30% was achieved. For the procedure of calculating the e{sup +}/e{sup -} track efficiencies a detailed study of RICH detector signals was performed, leading to an overall improved description of ring observables in the simulation. In total, 32545pm 385 e{sup +}e{sup -} signal pairs with an opening angle {alpha}{sub ee} > 15 and 0.1 < p{sub e} < 1.1 GeV/c were identified, with 7402{+-}222 pairs in the so-called {eta} mass region (0.15 < M{sub ee} < 0.55 GeV/c{sup 2}) and 253{+-}25 for masses M{sub ee} > 0.55 GeV/c{sup 2}. A clear signal from direct {omega} decay with S/B {proportional_to}1 was identified for the first time in the SIS18 energy regime. The extraction of the {omega} yield per produced {pi}{sup 0} results in N({omega})/N({pi}{sup 0}) {approx} (4,5 {+-} 2,5(stat) {+-} 2(sys)) .10{sup -8}. The e{sup +}e{sup -} production in the {eta} mass region was compared to the expected {eta} Dalitz decay {eta}{yields}{gamma}e{sup +}e{sup -} contribution. The measured e{sup +}e{sup -} yield is higher by a factor F = 3.4{+-}0.2(stat){+-}0.6(sys){+-}0.9({eta}) as compared to the {eta} production. The excitation function of the extra e{sup +}/e{sup -} sources shows similar energy

Effects of temperature, concentration, and uranium chloride mixture on zirconium electrochemical studies in LiCl−KCl eutectic salt

Energy Technology Data Exchange (ETDEWEB)

Hoover, Robert O. [Department of Chemical and Materials Engineering and Nuclear Engineering Program, University of Idaho, Center for Advanced Energy Studies, 995 University Blvd, Idaho Falls, ID 8340 (United States); Yoon, Dalsung [Department of Mechanical & Nuclear Engineering, Virginia Commonwealth University, 401 West Main St., Richmond, VA 23284 (United States); Phongikaroon, Supathorn, E-mail: sphongikaroon@vcu.edu [Department of Mechanical & Nuclear Engineering, Virginia Commonwealth University, 401 West Main St., Richmond, VA 23284 (United States)

2016-08-01

Experimental studies were performed to provide measurement and analysis of zirconium (Zr) electrochemistry in LiCl−KCl eutectic salt at different temperatures and concentrations using cyclic voltammetry (CV). An additional experimental set with uranium chloride added into the system forming UCl{sub 3}−ZrCl{sub 4}−LiCl−KCl was performed to explore the general behavior of these two species together. Results of CV experiments with ZrCl{sub 4} show complicated cathodic and anodic peaks, which were identified along with the Zr reactions. The CV results reveal that diffusion coefficients (D) of ZrCl{sub 4} and ZrCl{sub 2} as the function of temperature can be expressed as D{sub Zr(IV)} = 0.00046exp(−3716/T) and D{sub Zr(II)} = 0.027exp(−5617/T), respectively. The standard rate constants and apparent standard potentials of ZrCl{sub 4} at different temperatures were calculated. Furthermore, the results from the mixture of UCl{sub 3} and ZrCl{sub 4} indicate that high concentrations of UCl{sub 3} hide the features of the smaller concentration of ZrCl{sub 4} while Zr peaks become prominent as the concentration of ZrCl{sub 4} increases.

Radiation-stimulated yield of an impurity into interstitial sites in crystals KBr-Li and KCl-Li

International Nuclear Information System (INIS)

Bekeshev, A.Z.; Shunkeev, K.Sh.; Vasil'chenko, E.A.; Dauletbekova, A.K.; Ehlango, A.A.

1996-01-01

KCl and KBr crystals are taken as examples to show that the presence of Li impurity at X-radiation at temperatures above 200 K stimulates the creation of both impurity Hal 3 - (Li)-centers (V 4A -centers) and Hal 3 - centers (V 2 -centers). Increase of impurity concentration and X-radiation temperature (up to 300 K) results to increase of impurity stimulated creation of inherent Hal 3 - centers by more, than one order, as compared to pure crystals. Initial temperature of interstitial ion mobility was evaluated (about 140 K). 16 refs., 5 figs

High-speed detection of DNA translocation in nanopipettes

Science.gov (United States)

Fraccari, Raquel L.; Ciccarella, Pietro; Bahrami, Azadeh; Carminati, Marco; Ferrari, Giorgio; Albrecht, Tim

2016-03-01

We present a high-speed electrical detection scheme based on a custom-designed CMOS amplifier which allows the analysis of DNA translocation in glass nanopipettes on a microsecond timescale. Translocation of different DNA lengths in KCl electrolyte provides a scaling factor of the DNA translocation time equal to p = 1.22, which is different from values observed previously with nanopipettes in LiCl electrolyte or with nanopores. Based on a theoretical model involving electrophoresis, hydrodynamics and surface friction, we show that the experimentally observed range of p-values may be the result of, or at least be affected by DNA adsorption and friction between the DNA and the substrate surface.We present a high-speed electrical detection scheme based on a custom-designed CMOS amplifier which allows the analysis of DNA translocation in glass nanopipettes on a microsecond timescale. Translocation of different DNA lengths in KCl electrolyte provides a scaling factor of the DNA translocation time equal to p = 1.22, which is different from values observed previously with nanopipettes in LiCl electrolyte or with nanopores. Based on a theoretical model involving electrophoresis, hydrodynamics and surface friction, we show that the experimentally observed range of p-values may be the result of, or at least be affected by DNA adsorption and friction between the DNA and the substrate surface. Electronic supplementary information (ESI) available: Gel electrophoresis confirming lengths and purity of DNA samples, comparison between Axopatch 200B and custom-built setup, comprehensive low-noise amplifier characterization, representative I-V curves of nanopipettes used, typical scatter plots of τ vs. peak amplitude for the four LDNA's used, table of most probable τ values, a comparison between different fitting models for the DNA translocation time distribution, further details on the stochastic numerical simulation of the scaling statistics and the derivation of the extended

Conversion of impurity-vacancy complexes under γ-irradiation and subsequent F band bleaching in KCl:Eu2+

International Nuclear Information System (INIS)

Mladenova, M.; Malinovski, A.; Georgiev, M.

1982-01-01

The ESR signal from I-V complexes in KCl:Eu 2+ is found to decrease markedly as a result of γ-irradiation and to vary swing-wise on subsequent F band bleaching at RT. The main bleaching process is explained by the superposition of Z 1 centre formation and the revival of I-V complexes following photostimulated recombination of F centres with I-V-trapped interstitials. Evidence seems also to be obtained for Eu + formation at the initial bleaching stage. (author)

A basic study on capture and solidification of rare earth nuclide (Nd) in LiCl-KCl eutectic salt using an inorganic composite with Li{sub 2}OAl{sub 2}O{sub 3}- SiO{sub 2}-B{sub 2}O{sub 3} systems

Energy Technology Data Exchange (ETDEWEB)

Kim, Na Young; Eum, Hee Chul; Park, Hwan Seo; Ahn, Do Hee [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2017-03-15

The pyroprocessing of spent nuclear fuel generates LiCl-KCl eutectic waste salt containing radioactive rare earth nuclides. It is necessary to develop a simple process for the treatment of LiCl-KCl eutectic waste in a hot-cell facility. In this study, capture and solidification of a rare earth nuclide (Nd) in LiCl-KCl eutectic salt using an inorganic composite with a Li{sub 2}OAl{sub 2}O{sub 3}- SiO{sub 2}-B{sub 2}O{sub 3} system was conducted to simplify the existing separation and solidification process of rare earth nuclides in LiCl-KCl eutectic waste salt from the pyroprocessing of spent nuclear fuel. More than 98wt% of Nd in LiCl-KCl eutectic salt was captured when the mass ratio of the composite was 0.67 over NdCl3 in the eutectic salt. The content of Nd{sub 2}O{sub 3} in the Nd captured-composite reached about 50wt%, and this composite was directly fabricated into a homogeneous and chemical resistant glass waste in a monolithic form. These results will be utilized in designing a process to simplify the existing separation and solidification process.

Thermodynamic properties of (LiCl + N,N-dimethylacetamide) and (LiBr + N,N-dimethylacetamide) at temperatures from (323.15 to 423.15) K

Energy Technology Data Exchange (ETDEWEB)

Nasirzadeh, Karamat [Institut fuer Physikalische and Theoretische Chemie, Universitaet Regensburg, D-93040 Regensburg (Germany) and Department of Chemistry, Azarbaijan University of Tarbiat Moallem, Tabriz (Iran, Islamic Republic of)]. E-mail: Karamat.Nasirzadeh@chemie.uni-regensburg.de; Neueder, Roland [Institut fuer Physikalische and Theoretische Chemie, Universitaet Regensburg, D-93040 Regensburg (Germany); Kunz, Werner [Institut fuer Physikalische and Theoretische Chemie, Universitaet Regensburg, D-93040 Regensburg (Germany)

2005-04-15

Precise vapor pressure data for LiCl and LiBr solutions in N,N-dimethylacetamide are given for T = (323.15 to 423.15) K. The molality ranges covered in this study are about m = (0.073 to 1.89) mol . kg{sup -1} for lithium chloride and m = (0.06 to 1.75) mol . kg{sup -1} for lithium bromide. Osmotic coefficients are calculated by taking into account the second virial coefficient of N,N-dimethylacetamide. The parameters of the extended Pitzer-ion interaction model of Archer, of the MSA-NRTL model and of the chemical model of Barthel are evaluated. These models accurately reproduce the experimental osmotic coefficients within different concentration ranges. The parameters of the Pitzer-ion interaction model of Archer are used to calculate the mean molal activity coefficients and excess Gibbs free energies. The non-ideal behaviors of these systems are discussed in terms of the model parameters.

Preparing of LiCl-KCl-UCl3 eutectic salt by a chlorination of Cd

International Nuclear Information System (INIS)

Kang, Hee Seok; Woo, Moon Sik; Lee, Han Soo

2008-01-01

Uranium trichloride salt(UCl 3 ) is supplied with the initial U in to the LiCl-KCl eutectic salt for a stabilization of the initial cell voltage during an electrorefining process in a reactor. The apparatus for producing UCl 3 consists of a chlorine gas generator, a chlorinator, and an off-gas wet scrubber. Gaseous chlorine in the chlorine gas generator was injected into a lower layer of liquid Cd where CdCl 2 formed. The CdCl 2 reacts with the uranium to form uranium trichloride and Cd. The throughput of the UCl 3 chlorinator is about. 1.4Kg UCl 3 /batch. During a production the temperature of the reactants are maintained at about 600 .deg. C

On the impedance of galvanic cells XXIV. The impedance of the In3+/In(Hg) electrode reaction in KSCN and KCl solution

NARCIS (Netherlands)

Timmer, B.; Sluyters-Rehbach, M.; Sluyters, J.H.

1968-01-01

The In3+/In(Hg) system in KSCN and KCl solutions has been investigated using both d.c. and a.c. measurements. The experimental data are analysed and interpreted according to theoretical equations presented recently. It is shown that the specific adsorption of indium from 1 M KSCN follows a linear

Measurements of pressure for the TiH/sub x//KClO4 system

International Nuclear Information System (INIS)

Chong, C.H.H.; Glaub, J.E.

1978-01-01

An investigation was conducted to measure the pressure obtained when the pyrotechnic mixture TiH/sub x//KClO 4 was ignited in a confined variable-volume system. It was possible to derive an expression of the form PV/sup γ/ = k for the pressure-volume relationship obtained. This expression is a polytropic expansion of the ideal gas equation that best fits the data generated. For this particular work, values of γ = 0.53 and k = 69.3 were obtained where P is in megapascals and V is in cubic centimeters. In addition, estimates of the reaction rates were calculated based on the times to achieve maximum pressure for a given volume system. An explicit expression relating rate to pressure was derived by a simplified least-squares fit of the data obtained

Deficiency of electroneutral K+-Cl- cotransporter 3 causes a disruption in impulse propagation along peripheral nerves.

Science.gov (United States)

Sun, Yuan-Ting; Lin, Thy-Sheng; Tzeng, Shun-Fen; Delpire, Eric; Shen, Meng-Ru

2010-10-01

Nerve conduction requires the fine tuning of ionic currents through delicate interactions between axons and Schwann cells. The K(+)-Cl(-) cotransporter (KCC) family includes four isoforms (KCC1-4) that play an important role in the maintenance of cellular osmotic homeostasis via the coupled electroneutral movement of K(+) and Cl(-) with concurrent water flux. Mutation in SLC12A6 gene encoding KCC3 results in an autosomal recessive disease, known as agenesis of the corpus callosum associated with peripheral neuropathy. Nevertheless, the role of KCC3 in nerve function remains a puzzle. In this study, the microscopic examination of KCC isoforms expressed in peripheral nerves showed high expression of KCC2-4 in nodal segments of the axons and in the perinucleus and microvilli of Schwann cells. The KCC inhibitor [[(dihydroindenyl)oxy]alkanoic acid] but not the Na(+)-K(+)-2Cl(-)-cotransport inhibitor (bumetanide) dose-dependently suppressed the amplitude and area of compound muscle action potential, indicating the involvement of KCC activity in peripheral nerve conduction. Furthermore, the amplitude and area under the curve were smaller, and the nerve conduction velocity was slower in nerves from KCC3(-/-) mice than in nerves from wild-type mice, while the expression pattern of KCC2 and KCC4 was similar in KCC3 kockout and wild-type strains. KCC3(-/-) mice also manifested a prominent motor deficit in the beam-walking test. This is the first study to demonstrate that the K(+)-Cl(-) cotransporter activity of KCC3 contributes to the propagation of action potentials along peripheral nerves. (c) 2010 Wiley-Liss, Inc.

R and D activities on the management of waste chloride salts in KAERI

International Nuclear Information System (INIS)

In-Tae, Kim; Hwan-Seo, Park; Jeong-Gook, Kim; Hee-Chul, Yang; Yong-Joon, Cho; Eung-Ho Kim

2007-01-01

Full text of publication follows. Electrochemical treatment of spent oxide fuels has been intensively studied in KAERI to reduce the volume, heat load and radiotoxicity of high-level wastes. It consists of an electrolytic reduction process to convert the oxide fuel into a metallic form and an electro-refining process to separate TRU elements from the electro-reduced metal ingot. Two types of waste salts are expected to generate from the electrochemical pyro-processes, that is, LiCl salt from the reduction process and LiCl+KCl eutectic salt form the refining process. The R and D strategy of the waste salt management in KAERI can be categorized into two parts: 1) enhancement of safety by the stabilisation/solidification of waste salt that is to be finally disposed of and 2) reduction of the waste generation by the regeneration/recycle of the spent salt after removal of radionuclides in it. A sol-gel technique and a zeolite occlusion technique are under development to stabilize the waste salt. The LiCl salt is stabilised by a low-temperature sol-gel process and then the gel product is solidified into a ceramic-like waste form with an addition of glass frit. Another method uses Zeolite-4A to occlude the LiCl salt into its cage and adsorption site to immobilize the radionuclides. The product, salt-occluded zeolite, is fabricated into another type of a ceramic waste form. For the regeneration and recycle of the spent salt, the radionuclides in the salt are removed by a zeolite process for the LiCl salt and by an oxidation/distillation process for the eutectic salt. The target nuclides to be removed in each process are Cs/Sr and rare earth (RE) elements, respectively. In the oxidation/ distillation process, the rare earth chloride nuclides are oxidised by an oxygen sparging method, and the products are precipitated in the form of oxide or oxychloride REs. After separation of the RE elements from the precipitates by distillation, the refined spent salt with a low content

THE DISTRIBUTION OF COMMERCIAL CROWN ETHER DC18C6 AND THE EXTRACTION STUDY OF ALKALI AND EARTH ALKALI METALS

Directory of Open Access Journals (Sweden)

Bambang Rusdiarso

2010-06-01

Full Text Available Distribution of A and B isomers of crown-ether DC18C6 on their organic and water phases (chloride, nitrate and sulphocyanide salts and extraction of alkali and earth alkali metals has been studied. In LiCl 0.1 M environment, lithium extraction could be ignored. The presence of extracted potassium metal may affect the crown ether DC18C6 distribution albeit only a little. In KNO3 0.1 M environment, the distribution coefficient values (d were 6.1 and 10.3 for A and B isomers, respectively ; while in KCl  0.1 M environment the values were 4.9 and 11.8, respectively. In KSCN 0.1 M, d values for A and B isomers were 40.4 and 36.6, respectively, which were higher than the value obtained from both KNO3 and KCl  0.1 M environments. Caesium metal extraction using DC18C6 occurred weakly, up to only 5%. Strontium extraction using DC18C6 achieved better yield than the caesium extraction. The percentage of extraction increased under organic solvent according to the following: toluene (4% < chloroform (28% < TBP (35%.   Keywords: distribution, crown-ether DC18C6, extraction.

Electroanalytical measurements of binary-analyte mixtures in molten LiCl-KCl eutectic: Uranium(III)- and Magnesium(II)-Chloride

Energy Technology Data Exchange (ETDEWEB)

Rappleye, Devin, E-mail: rappleye1@llnl.gov; Newton, Matthew L.; Zhang, Chao; Simpson, Michael F.

2017-04-01

The electrochemical behavior of MgCl{sub 2} in molten LiCl-KCl eutectic was investigated to evaluate its suitability as a surrogate for PuCl{sub 3} in studies related to the eletrorefining of used nuclear fuel. The reduction of Mg{sup 2+} was found to be electrochemically reversible up to 300 mV s{sup −1} at 773 K. The diffusion coefficient for Mg{sup 2+} was calculated to be 1.74 and 2.17 × 10{sup −5} cm{sup 2} s{sup −1} with and without U{sup 3+} present, respectively, at 773 K using cyclic voltammetry (CV). Upon comparison to literature data, the diffusion coefficient of Mg{sup 2+} differs by only 8.8% (with U{sup 3+} present) from that of Pu{sup 3+} and the difference in peak potentials was only 79 mV. Binary-analyte mixtures of UCl{sub 3} and MgCl{sub 2} in eutectic LiCl-KCl were further investigated using CV, normal pulse voltammetry (NPV), chronoamperometry (CA) and open-circuit potential (OCP) measurements for the purpose of comparing each technique's accuracy in measuring U{sup 3+} and Mg{sup 2+} concentrations. Of all the techniques tested, NPV resulted in the lowest error which was, on average, 11.4% and 9.81% for U{sup 3+} and Mg{sup 2+}, respectively.

EFFECT OF GRAIN SIZE AND ACTIVATION TIME OF ZEOLITE TO ADSORPTION AND DESORPTION OF NH4OH AND KCL AS MODEL OF FERTILIZER-ZEOLITE MIX

Directory of Open Access Journals (Sweden)

Muhammad Prasantio Bimantio

2017-10-01

Full Text Available Zeolites can be used as adsorbent, ion exchange, catalyst, or catalyst carrier. Application of fertilizer use in the zeolite also be one of the interesting topic. Zeolites in a mixture of fertilizer can use to control the release of nutrients. The purpose of this research is to study the effect of grain size and time of the activation of zeolite to adsorption and desorption of NH4OH and KCl as modeling of ZA and KCl fertilizer, to obtain the value of adsorption rate constant (ka and desorption rate constant (kd. This research procedure include: the process of adsorption by adding zeolite with various size and time of activation into a sealed beaker glass and let the adsorption process occurs for 24 hours. After 24 hours, the solution was filtered, the zeolite then put in 100 ml of aquadest into a sealed beaker glass and let the desorption process happened for another 24 hours. Three samples with the largest difference solution concentrations looked for the value of the ka and kd. Zeolite configuration with the largest ka is trialed with fertilizer and compared with the value of ka obtained from modeling. The result for NH4OH adsorbate, -50+60 mesh 2 hours configuration zeolite give the largest ka. For KCl adsorbate, -30+40 mesh 4 hours configuration zeolite give the largest ka. The value between modeling and trials with fertilizers are not much different.

Reduction behavior of UO{sub 2}{sup 2+} in molten LiCl–RbCl and LiCl–KCl eutectics by using tungsten

Energy Technology Data Exchange (ETDEWEB)

Nagai, Takayuki, E-mail: nagai.takayuki00@jaea.go.jp [Nuclear Fuel Cycle Engineering Lab., Japan Atomic Energy Agency, Muramatsu, Tokai, Naka, Ibaraki 319-1194 (Japan); Uehara, Akihiro; Fujii, Toshiyuki; Yamana, Hajimu [Research Reactor Institute, Kyoto University, Asashironishi, Kumatori, Sen-nan, Osaka 590-0494 (Japan)

2013-08-15

The reduction of uranium from UO{sub 2}{sup 2+} to UO{sub 2}{sup +} or U{sup 4+} in molten LiCl–RbCl and LiCl–KCl eutectics was examined by using tungsten and chlorine gas. Spectrophotometric technique was adopted to determine the concentration of uranium species. When tungsten was immersed into the LiCl–RbCl eutectic melt at 400 °C without supplying chlorine gas, 36% of the total weight of the hexavalent of UO{sub 2}{sup 2+} was reduced to the pentavalent of UO{sub 2}{sup +}. Under purging chlorine gas into the melt, 96% of UO{sub 2}{sup 2+} was reduced to the tetravalent of U{sup 4+}. Tungsten oxy-chloride of WOCl{sub 4} was produced via the reductions of UO{sub 2}{sup 2+}, which was volatized from the melt and adsorbed on the upper part of experimental cell. On the other hand, 84% of UO{sub 2}{sup 2+} in the LiCl–KCl eutectic melt at 500 °C was reduced to U{sup 4+} by using tungsten and chlorine gas.

Concentration quenching of F{sub a}(II) emission in KCl:Li

Energy Technology Data Exchange (ETDEWEB)

Baldacchini, G.; Giovenale, E. [ENEA, Centro Ricerche Frascati, Rome (Italy). Dip. Innovazione; Grassano, U.M. [Rome Univ. `Tor Vergata` (Italy); Scacco, A. [Rome Univ. `La Sapienza` (Italy)

1996-12-01

The concentration quenching of luminescence is a well known phenomenon for the F centers in alkali halides. On the contrary very little is known on this subject for F{sub A} centers which are a class of axial color centers still of some importance both in basic and applied research, for instance as color center laser sources. The authors have studied carefully the optical properties of the F{sub A}(II) centers, especially in KCl:Li in extreme physical conditions, such as high F{sub A} concentration, high optical pumping, low temperatures and high magnetic fields, and, among other results, a new weak luminescence has been found at 1.4 {mu}m. At moment is not yet clear whether this emission is related to the concentration quenching itself or to more complex color centers, among them F{sub A}(I) centers. However, general hypothesis and reliable measurements are proposed in order to clarify the still unknown microscopic mechanisms which reduces the emission intensity of the F{sub A}(II) centers when they are highly concentrated.

Semiconductor- to metallic-like behavior in Bi thin films on KCl substrate

International Nuclear Information System (INIS)

Bui, Thanh Nhan; Raskin, Jean-Pierre; Hackens, Benoit

2016-01-01

Bi thin films, with a thickness of 100 nm, are deposited by electron-beam evaporation on a freshly cleaved (100) KCl substrate. The substrate temperature during film growth (T_d_e_p) ranges from room temperature up to 170 °C. Films deposited at room temperature exhibit a maze-like microstructure typical of the rhombohedral (110) texture, as confirmed by X-ray diffraction. For T_d_e_p above 80 °C, a different microstructure appears, characterized by concentric triangular shapes corresponding to the trigonal (111) texture. Temperature dependence of the resistivity shows a transition from a semiconductor-like behavior for films deposited at room temperature to a metallic-like behavior for T_d_e_p above 80 °C. From magnetoresistance measurements between room temperature and 1.6 K, we extract the electron and hole mobilities, concentrations, and mean free paths, which allow to draw a complete picture of the transport properties of both types of films.

Ionic thermocurrent and optical-absorption measurements in KCl: Sr under reactor irradiation

International Nuclear Information System (INIS)

Sordi, G.M.; Watanabe, S.

1976-01-01

Radiation damage in KCl crystals doped with Sr ++ using thermionic-current techniques (ITC) and optical-absorption measurements is studied. Analysing the radiation damage due to three different gamma ray exposures, namely the gamma irradiation, creates F-type or V-type colour centres and destroys a fraction of impurity-vacancy dipoles. Fast neutron irradiation added to the gamma irradiation increases the efficiency of destruction of dipoles and also provoke the appearence of a second ITC peak at temperatures neat 123 0 K, which is unstable and disappears in a few days. On the other hand, thermal neutrons bombarding the samples together with fast neutrons and gamma-rays leave unchanged the impurity-vacancy dipole concentration obtained after the gamma plus fast neutron irradiation. With thermal neutrons there is a high background current, and the peak resolution is only possible when thermally and electrostatically polarizable electrical carriers have largely disappeared. For this reason it is impossible to compare the 123 0 K peak obtained with and without thermal neutrons

Thermoluminescent monitoring of the solar ultraviolet radiation with KCl: Eu2+ crystals

International Nuclear Information System (INIS)

Chernov, V.; Melendrez, R.; Barboza F, M.

2000-01-01

In this work it has been investigating the Tl properties of KCl: Eu 2+ subjected to solar direct radiation. Also it was realized irradiation with the Deuterium and Xenon lamps. It was used a set of filters and a Katos monochromator 0.25 M to determine the spectral response to Tl peaks and a study of them with respect to the duration of the Sun irradiation. After of the Sun irradiation the Tl curves show several peaks between the ambient temperature and 673 K. The relation between peaks depends strongly of the irradiation time and the different solar light wavelength. It is possible to divide the Tl peaks in two groups. The first one (T 473 K) is not too sensitive but is more stable under optical whitening. Here the obtained results are discussed with respect to UV dosemeters development for environment which facilitate to obtain direct measurements of the UV index. (Author)

Thermoluminescent monitoring of the solar ultraviolet radiation with KCl: Eu{sup 2+} crystals; Monitoreo termoluminiscente de la radiacion solar ultravioleta con cristales de KCl: Eu{sup 2+}

Energy Technology Data Exchange (ETDEWEB)

Chernov, V.; Melendrez, R.; Barboza F, M. [Centro de Investigacion en Fisica, Universidad de Sonora, A.P. 5-88, Hermosillo, Sonora (Mexico)

2000-07-01

In this work it has been investigating the Tl properties of KCl: Eu{sup 2+} subjected to solar direct radiation. Also it was realized irradiation with the Deuterium and Xenon lamps. It was used a set of filters and a Katos monochromator 0.25 M to determine the spectral response to Tl peaks and a study of them with respect to the duration of the Sun irradiation. After of the Sun irradiation the Tl curves show several peaks between the ambient temperature and 673 K. The relation between peaks depends strongly of the irradiation time and the different solar light wavelength. It is possible to divide the Tl peaks in two groups. The first one (T<473 K) is very sensitive to ultraviolet radiation but it is strongly affected by visible light. The second one (T>473 K) is not too sensitive but is more stable under optical whitening. Here the obtained results are discussed with respect to UV dosemeters development for environment which facilitate to obtain direct measurements of the UV index. (Author)

Generation of KCL018 research grade human embryonic stem cell line carrying a mutation in the DMPK gene

Directory of Open Access Journals (Sweden)

Cristian Miere

2016-03-01

Full Text Available The KCL018 human embryonic stem cell line was derived from an embryo donated for research that carried an autosomal dominant mutation affecting one allele of the DMPK gene encoding the dystrophia myotonica protein kinase (2200 trinucleotide repeats; 14 for the normal allele. The ICM was isolated using laser microsurgery and plated on γ-irradiated human foreskin fibroblasts. Both the derivation and cell line propagation were performed in an animal product-free environment. Pluripotent state and differentiation potential were confirmed by in vitro assays.

Generation of KCL028 research grade human embryonic stem cell line carrying a mutation in the HTT gene

Directory of Open Access Journals (Sweden)

Laureen Jacquet

2016-03-01

Full Text Available The KCL028 human embryonic stem cell line was derived from an embryo donated for research that carried an autosomal dominant mutation affecting one allele of the HTT gene encoding huntingtin (43 trinucleotide repeats; 21 for the normal allele. The ICM was isolated using laser microsurgery and plated on γ-irradiated human foreskin fibroblasts. Both the derivation and cell line propagation were performed in an animal product-free environment. Pluripotent state and differentiation potential were confirmed by in vitro and in vivo assays.

Quantifying Local and Cooperative Components in the Ferroelectric Distortion of BaTiO3: Learning from the Off-Center Motion in the MnCl65– Complex Formed in KCl:Mn+

DEFF Research Database (Denmark)

García Lastra, Juan Maria; García-Fernández, P.; Calle-Vallejo, F.

2014-01-01

→ C4v → Oh local transformations occurring in the 10–50 K temperature range for the MnCl65– complex formed in KCl:Mn+ that mimic the behavior of BaTiO3. From Boltzmann analysis of the vibronic levels derived from ab initio calculations and considering decoherence introduced by random strains......, the present calculations reproduce the experimental phase sequence and transition temperatures. Furthermore, our calculations show that the off-center instability in KCl:Mn+ would be suppressed by reducing by only 1% the lattice parameter, a situation that then becomes comparable to that found for BaTiO3...

n-particle transverse correlation and collectivity for collisions 1.2 A GeV Ar + KCl

International Nuclear Information System (INIS)

Liu Qingjun; Jiang Yuzhen; Wang Shan; Liu Yiming; Fung, S.Y.; Chu, S.Y.

1993-01-01

A method of n-particle transverse correlation function for the study of collective flow is proposed, which extends both the study of n-particle azimuthal correlations and the estimation of collectivity to the study including the magnitudes as well as the azimuthal angles for all the n-particle transverse momentum vectors. This method is more sensitive to the collectivity of collective flow than the method based on multi-particle azimuthal correlations. Using the new method, n-particle transverse correlations are analyzed for collisions of 1.2 A GeV Ar + KCl in the Bevalac streamer chamber, and the results have been compared with a Monte-Carlo simulation, which show that the collectivity for this experiment is between 85% and 95%

Comparative study of the thermoluminescence between the materials α-Al2O3:C, KCl:Eu2+, KBr: Eu2+ and VYCOR

International Nuclear Information System (INIS)

Pedroza M, M.; Melendrez, R.; Perez S, R.; Aceves, R.; Piters, T.M.; Barboza F, M.

1999-01-01

It is presented some investigation results related to the thermoluminescence curves (Tl), Tl emission and the spectra of excitation of thermoluminescence in the ultraviolet region of 190 to 250 nm in the materials α-Al 2 O 3 :C, KCl: Eu 2+ , KBr: Eu 2+ and the Vycor glass. It was able to be observed that the Tl emission for the first three materials exists around 420 nm and in the case of Vycor the emission consists of two Tl peaks where the most low temperature is a band more wide centered in 460 nm and the other band of high temperature emits in 470 nm. In the excitation curves of Tl were obtained centered bands around 230 nm for KCl: Eu 2+ , 235 nm for KBr: Eu 2+ , 220 nm for the alumina and 195 nm for the Vycor. From the results it was able to be appreciated that this last has a minor relative intensity with respect to the others materials but also the region in which works there was an alone band between the 190 to 205 nm. This fact makes the material be very selective in the ultraviolet region of greatest energy. (Author)

GIFAD for He/KCl(001). Structure in the pattern for 〈 110 〉 incidence as a measure of the projectile-cation interaction

Science.gov (United States)

Bocan, G. A.; Gravielle, M. S.

2018-04-01

In this article we address grazing incidence fast atom diffraction (GIFAD) for the He/KCl(001) system, for which a systematic experimental study was recently reported [E. Meyer, Ph.D dissertation, Humboldt-Universität, Berlin, Germany, 2015]. Our theoretical model is built from a projectile-surface interaction obtained from Density Functional Theory (DFT) calculations and the Surface Initial-Value Representation (SIVR), which is a semi-quantum approach to describe the scattering process. For incidence along the 〈 100 〉 and 〈 110 〉 directions, we present and discuss the main features of our interaction potential, the dependence of the rainbow angle with the impact energy normal to the surface, and the simulated GIFAD patterns, which reproduce the main aspects of the reported experimental charts. The features of the diffraction charts for He/KCl(001) are related to the averaged equipotential curves of the system and a comparison is established with the case of He/LiF(001). The marked differences observed for 〈 110 〉 incidence are explained as due to the much larger size of the K+ ion relative to that of Li+.

Electro-separation of actinides using Al cathodes in LiCl-KCl

Energy Technology Data Exchange (ETDEWEB)

Serp, J.; Malmbeck, R.; Scheppler, C.; Glatz, J.P

2004-07-01

In this work, the reprocessing of a simulated spent fuel (U{sub 60}Pu{sub 20}Zr{sub 10}Am{sub 2}Nd{sub 3.5}Y{sub 0.5}Ce{sub 0.5}Gd{sub 0.5}) have been studied by electrolysis in molten chloride salt on a solid Al cathode. The electrorefining was carried out under constant current at 733 Kin LiCl-KCl eutectic. In one electrolysis of 1386 C, a total of 1.13 g of actinides were recovered as alloy on the Al cathode. The obtained deposit was dissolved in HNO{sub 3} (7 M) and analysed by ICP-MS. The deposit was found to be composed mainly of U (90.3 %), Pu (9.3 %) and Am (0.3 %). The mass balance indicated a faradic yield close to 100%. The U/Nd, Pu/Nd and Am/Nd ratios in the deposit were 2800, 290 and 10, respectively. Therefore excellent separation of U and Pu was obtained and a separation of MA from Ln seems to be possible even with a low initial Am/Nd concentration ratio (0.41) in the salt phase. (authors)

Thermoluminescence of Z1 centres in Sr-doped KCl

International Nuclear Information System (INIS)

Kamavisdar, V.S.; Moholkar, S.C.; Deshmukh, B.T.

1980-01-01

It is well known for alkali halides doped with divalent metal impurities that exposure to high energetic radiation and subsequent F band bleaching leads to the formation of Z 1 centres. Optical absorption measurements have shown that a low concentration of Z 1 centres is produced along with F centres during irradiation without any optical bleaching. Now the question is whether Z 1 centres are really formed along with F centres during irradiation. The aim of the present paper was to study the formation of a small amount of Z 1 centres during irradiation with the help of optical absorption and thermoluminescence measurements. The crystals of KCl:Sr were exposed to γ-rays for different doses. The TL curve for the crystal exposed to a minimum dose of γ-rays shows a TL peak at 457 K and a weak shoulder in the region 400 K to 408 K. The TL curve of the crystal exposed to maximum dose of rays shows the peak at 408 K with a greater intensity. Upon F band bleaching 408 K peak increases in intensity and optical absorption is also broadened. It is shown that the peak at 457 K is due to F centres and the peak at 408 K is due to Z 1 centres. These results clearly show that a small anount of Z 1 centres is really formed along with F centres during irradiation. (author)

Separation of actinides from irradiated An–Zr based fuel by electrorefining on solid aluminium cathodes in molten LiCl–KCl

Energy Technology Data Exchange (ETDEWEB)

Souček, P., E-mail: Pavel.Soucek@ec.europa.eu [European Commission, Joint Research Centre (JRC), Institute for Transuranium Elements (ITU), Postfach 2340, 76125 Karlsruhe (Germany); Murakami, T. [Central Research Institute of Electric Power Industry (CRIEPI), Komae-shi, Tokyo 201-8511 (Japan); Claux, B.; Meier, R.; Malmbeck, R. [European Commission, Joint Research Centre (JRC), Institute for Transuranium Elements (ITU), Postfach 2340, 76125 Karlsruhe (Germany); Tsukada, T. [Central Research Institute of Electric Power Industry (CRIEPI), Komae-shi, Tokyo 201-8511 (Japan); Glatz, J.-P. [European Commission, Joint Research Centre (JRC), Institute for Transuranium Elements (ITU), Postfach 2340, 76125 Karlsruhe (Germany)

2015-04-15

Highlights: • Electrorefining process in molten LiCl-KCl using solid Al electrodes was demonstrated. • High separation factors of actinides over lanthanides were achieved. • Efficient recovery of actinides from irradiated nuclear fuel was achieved. • Uniform, dense and well adhered deposits were obtained and characterised. • Kinetic parameters of actinide–aluminium alloy formation were evaluated. - Abstract: An electrorefining process for metallic spent nuclear fuel treatment is being investigated in ITU. Solid aluminium cathodes are used for homogeneous recovery of all actinides within the process carried out in molten LiCl–KCl eutectic salt at a temperature of 500 °C. As the selectivity, efficiency and performance of solid Al has been already shown using un-irradiated An–Zr alloy based test fuels, the present work was focused on laboratory-scale demonstration of the process using irradiated METAPHIX-1 fuel composed of U{sub 67}–Pu{sub 19}–Zr{sub 10}–MA{sub 2}–RE{sub 2} (wt.%, MA = Np, Am, Cm, RE = Nd, Ce, Gd, Y). Different electrorefining techniques, conditions and cathode geometries were used during the experiment yielding evaluation of separation factors, kinetic parameters of actinide–aluminium alloy formation, process efficiency and macro-structure characterisation of the deposits. The results confirmed an excellent separation and very high efficiency of the electrorefining process using solid Al cathodes.

The study of some physico-chemical properties of melt KCl - NaCl mixture

Directory of Open Access Journals (Sweden)

Vojtech Špeťuch

2013-03-01

Full Text Available The aim of this paper was to examine the surface tension of the melt mixture of salts NaCl and KCl at temperatures 750, 800 and 850 °C by maximum bubble pressure method. Some difference between measured values of the surface tension as dependence on the method of calculation was observed. This difference results from the diameter of used capillary and does not depend on the temperature. The differences between experimentally measured values of surface tension and literary sources are trivial. The experimental results are in accordance with the literature data confirming unsuitability of maximum bubble pressure method for measurement of the melt density. The experimental result will be used as a base for the study of melt salts ternary systems. On the other side maximum bubble pressure method is the most suitable method for measurement of surface tension of melt salts, but it is unsuitable for measurement of the melt density.

Generation of KCL025 research grade human embryonic stem cell line carrying a mutation in NF1 gene

Directory of Open Access Journals (Sweden)

Heema Hewitson

2016-03-01

Full Text Available The KCL025 human embryonic stem cell line was derived from an embryo donated for research that carried an autosomal dominant mutation in the NF1 gene encoding neurofibromin (c.3739–3742 ΔTTTG. Mutations in this gene have been linked to neurofibromatosis type 1, juvenile myelomonocytic leukemia and Watson syndrome. The ICM was isolated using laser microsurgery and plated on γ-irradiated human foreskin fibroblasts. Both the derivation and cell line propagation were performed in an animal product-free environment. Pluripotent state and differentiation potential were confirmed by in vitro assays.

Electrochemical formation of AlN in molten LiCl-KCl-Li{sub 3}N systems

Energy Technology Data Exchange (ETDEWEB)

Goto, Takuya [Department of Fundamental Energy Science, Graduate School of Energy Science, Kyoto University, Sakyo, Kyoto 606-8501 (Japan)]. E-mail: goto@energy.kyoto-u.ac.jp; Iwaki, Takayuki [Department of Fundamental Energy Science, Graduate School of Energy Science, Kyoto University, Sakyo, Kyoto 606-8501 (Japan); Ito, Yasuhiko [Department of Fundamental Energy Science, Graduate School of Energy Science, Kyoto University, Sakyo, Kyoto 606-8501 (Japan)

2005-01-30

Electrochemical formation of aluminum nitride was investigated in molten LiCl-KCl-Li{sub 3}N systems at 723 K. When Al was anodically polarized at 1.0 V (versus Li{sup +}/Li), oxidation of nitride ions proceeded to form adsorbed nitrogen atoms, which reacted with the surface to form AlN film. The obtained nitrided film had a thickness of sub-micron order. The obtained nitrided layer consisted of two regions; the outer layer involving AlN and aluminum oxynitride and the inner layer involving metallic Al and AlN. When Al electrode was anodically polarized at 2.0 V, anodic dissolution of Al electrode occurred to give aluminum ions, which reacted with nitride ions in the melt to produce AlN particles (1-5 {mu}m of diameter) of wurtzite structure.

Human NKCC2 cation–Cl– co-transporter complements lack of Vhc1 transporter in yeast vacuolar membranes.

Science.gov (United States)

Petrezselyova, Silvia; Dominguez, Angel; Herynkova, Pavla; Macias, Juan F; Sychrova, Hana

2013-10-01

Cation–chloride co-transporters serve to transport Cl– and alkali metal cations. Whereas a large family of these exists in higher eukaryotes, yeasts only possess one cation–chloride co-transporter, Vhc1, localized to the vacuolar membrane. In this study, the human cation–chloride co-transporter NKCC2 complemented the phenotype of VHC1 deletion in Saccharomyces cerevisiae and its activity controlled the growth of salt-sensitive yeast cells in the presence of high KCl, NaCl and LiCl. A S. cerevisiae mutant lacking plasma-membrane alkali–metal cation exporters Nha1 and Ena1-5 and the vacuolar cation–chloride co-transporter Vhc1 is highly sensitive to increased concentrations of alkali–metal cations, and it proved to be a suitable model for characterizing the substrate specificity and transport activity of human wild-type and mutated cation–chloride co-transporters. Copyright © 2013 John Wiley & Sons, Ltd.

Stability of zirconia sol in the presence of various inorganic electrolytes

Directory of Open Access Journals (Sweden)

Marković Jelena P.

2013-01-01

Full Text Available Zirconia sol was prepared from zirconium oxychloride solutions by forced hydrolysis at 102ºC. The prepared sol consisted of almost spherical, monoclinic, hydrated zirconia particles 61 nm in diameter. The stability of zirconia sol in the presence of various inorganic electrolytes (LiCl, NaCl, KCl, CsCl, KBr, KI, KNO3, and K2SO4 was studied by potentiometric titration method. Dependence of the critical concentration of coagulation (CCC on the dispersion pH was determined for all studied electrolytes. The critical coagulation concentration values, for all investigated electrolytes, are lower at higher pH. These values for all 1:1 electrolytes are equal in the range of experimental error. For a given pH value, CCCs of K2SO4 are 3-4 orders of magnitude lower than the corresponding values for 1:1 electrolytes. [Projekat Ministarstva nauke republike Srbije, br. III 45012

High-temperature corrosion of metals in the salt and metallic melts containing rare earths

Science.gov (United States)

Karpov, V. V.; Abramov, A. V.; Zhilyakov, A. Yu.; Belikov, S. V.; Volkovich, V. A.; Polovov, I. B.; Rebrin, O. I.

2016-09-01

A complex of independent methods was employed to study the corrosion resistance of molybdenum, zirconium, tantalum and tungsten in chloride, chloride-fluoride and fluoride-oxide melts based on LiCl, CaCl2, NaCl- KCl, LiF, and containing rare earths. Tests were conducted for 30 h at 750-1050 °C. The metals showed excellent corrosion resistance in fused chlorides (the corrosion rates were below 0.0005 g/(m2 h). Despite the presence of chemically active fluoride ions in the chloride-fluoride melts, the metals studied also showed very low corrosion rates, except molybdenum, for which the rate of corrosion was 0,8 g/(m2 h). The corrosion resistance of tantalum was considerably reduced in the fluoride-oxide melts; the corrosion rate was over 1 g/(m2 h) corresponding to the 8-th grade of stability and placing tantalum to the group of "low stability" materials.

Electrochemical behaviour of ThF4 in LiCl-KCl eutectic

International Nuclear Information System (INIS)

Agarwal, Renu; Mukerjee, S.K.; Ramakumar, K.L.

2016-01-01

Pyrochemical processing of nuclear fuels is an integral part of molten salt reactor technology. Thorium containing molten salt reactors are relevant for transmutation of minor actinides and utilizations of vast thorium resources. Understanding chemical and electrochemical behavior of actinide and lanthanide ions in chloride melts is an important task in this process. A eutectic of lithium and potassium chloride is found to be the most suitable salt for this study due to its low melting, high reduction potential and significant solubility of most of the actinide and lanthanide salts. However, electrochemistry of thorium in chloride melt is inconsistent due to dispute over the presence of Th(II) cation along with Th(IV). In the present experiments, cyclic-voltammograms of ThF 4 in LiCl-KCl eutectic salt were measured using three electrodes cell, where all the electrodes were 1 mm molybdenum wires and counter electrode wire was twisted into a spiral shape to increase surface area and was used for mixing the salts in molten state. Cyclic-voltammograms of pure eutectic melt and with ThF 4 were measured at scanning rates 50-300 mV/s, at 648 K and 723 K. Diffusion coefficient of Th 4+ was calculated using Delahay equation

Molten salt corrosion behavior of structural materials in LiCl-KCl-UCl3 by thermogravimetric study

Science.gov (United States)

Rao, Ch Jagadeeswara; Ningshen, S.; Mallika, C.; Mudali, U. Kamachi

2018-04-01

The corrosion resistance of structural materials has been recognized as a key issue in the various unit operations such as salt purification, electrorefining, cathode processing and injection casting in the pyrochemical reprocessing of spent metallic nuclear fuels. In the present work, the corrosion behavior of the candidate materials of stainless steel (SS) 410, 2.25Cr-1Mo and 9Cr-1Mo steels was investigated in molten LiCl-KCl-UCl3 salt by thermogravimetric analysis under inert and reactive atmospheres at 500 and 600 °C, for 6 h duration. Insignificant weight gain (less than 1 mg/cm2) in the inert atmosphere and marginal weight gain (maximum 5 mg/cm2) in the reactive atmosphere were observed at both the temperatures. Chromium depletion rates and formation of Cr-rich corrosion products increased with increasing temperature of exposure in both inert and reactive atmospheres as evidenced by SEM and EDS analysis. The corrosion attack by LiCl-KCl-UCl3 molten salt, under reactive atmosphere for 6 h duration was more in the case of SS410 than 9Cr-1Mo steel followed by 2.25Cr-1Mo steel at 500 °C and the corrosion attack at 600 °C followed the order: 9Cr-1Mo steel >2.25Cr-1Mo steel > SS410. Outward diffusion of the minor alloying element, Mo was observed in 9Cr-1Mo and 2.25Cr-1Mo steels at both temperatures under reactive atmosphere. Laser Raman spectral analysis of the molten salt corrosion tested alloys under a reactive atmosphere at 500 and 600 °C for 6 h revealed the formation of unprotected Fe3O4 and α-as well as γ-Fe2O3. The results of the present study facilitate the selection of structural materials for applications in the corrosive molten salt environment at high temperatures.

A kinetic study on the catalysis of KCl, K2SO4, and K2CO3 during oxy-biomass combustion.

Science.gov (United States)

Deng, Shuanghui; Wang, Xuebin; Zhang, Jiaye; Liu, Zihan; Mikulčić, Hrvoje; Vujanović, Milan; Tan, Houzhang; Duić, Neven

2018-07-15

Biomass combustion under the oxy-fuel conditions (Oxy-biomass combustion) is one of the approaches achieving negative CO 2 emissions. KCl, K 2 CO 3 and K 2 SO 4 , as the major potassium species in biomass ash, can catalytically affect biomass combustion. In this paper, the catalysis of the representative potassium salts on oxy-biomass combustion was studied using a thermogravimetric analyzer (TGA). Effects of potassium salt types (KCl, K 2 CO 3 and K 2 SO 4 ), loading concentrations (0, 1, 3, 5, 8 wt%), replacing N 2 by CO 2 , and O 2 concentrations (5, 20, 30 vol%) on the catalysis degree were discussed. The comparison between TG-DTG curves of biomass combustion before and after water washing in both the 20%O 2 /80%N 2 and 20%O 2 /80%CO 2 atmospheres indicates that the water-soluble minerals in biomass play a role in promoting the devolatilization and accelerating the char-oxidation; and the replacement of N 2 by CO 2 inhibits the devolatilization and char-oxidation processes during oxy-biomass combustion. In the devolatilization stage, the catalysis degree of potassium monotonously increases with the increase of potassium salt loaded concentration. The catalysis degree order of the studied potassium salts is K 2 CO 3  > KCl > K 2 SO 4 . In the char-oxidation stage, with the increase of loading concentration the three kinds of potassium salts present inconsistent change tendencies of the catalysis degree. In the studied loading concentrations from 0 to 8 wt%, there is an optimal loading concentration for KCl and K 2 CO 3 , at 3 and 5 wt%, respectively; while for K 2 SO 4 , the catalysis degree on char-oxidation monotonically increases with the loading potassium concentration. For most studied conditions, regardless of the potassium salt types or the loading concentrations or the combustion stages, the catalysis degree in the O 2 /CO 2 atmosphere is stronger than that in the O 2 /N 2 atmosphere. The catalysis degree is also affected by the O 2

Development and characterization of new high-level waste form containing LiCl KCl eutectic salts for achieving waste minimization from pyroprocessing

International Nuclear Information System (INIS)

Cho, Yong Zun; Kim, In Tae; Park, Hwan Seo; Ahn, Byeung Gil; Eun, Hee Chul; Son, Seock Mo; Ah, Su Na

2011-12-01

The purpose of this project is to develop new high level waste (HLW) forms and fabrication processes to dispose of active metal fission products that are removed from electrorefiner salts in the pyroprocessing based fuel cycle. The current technology for disposing of active metal fission products in pyroprocessing involves non selectively discarding of fission product loaded salt in a glass-bonded sodalite ceramic waste form. Selective removal of fission products from the molten salt would greatly minimize the amount of HLW generated and methods were developed to achieve selective separation of fission products during a previous I NERI research project (I NERI 2006 002 K). This I NERI project proceeds from the previous project with the development of suitable waste forms to immobilize the separated fission products. The Korea Atomic Energy Research Institute (KAERI) has focused primarily on developing these waste forms using surrogate waste materials, while the Idaho National Laboratory (INL) has demonstrated fabrication of these waste forms using radioactive electrorefiner salts in hot cell facilities available at INL. Testing and characterization of these radioactive materials was also performed to determine the physical, chemical, and durability properties of the waste forms

Direct preparation of Al-base alloys from their oxides/metal precursors in the eutectic LiCl–KCl melt

International Nuclear Information System (INIS)

Gao, Bingliang; Zhu, Hao; Xia, Yuxiang; Shi, Zhongning; Hu, Xianwei; Wang, Zhaowen

2016-01-01

A study was carried out on the preparation of Al–Cu–Li alloy from their oxides/metal precursors using the method of electro-deoxidation in the eutectic LiCl–KCl melt at 648 K. Cyclic voltammetry was used to characterize the system. The samples were prepared by potentiostatic electrolysis at −1.0 V to −2.0 V (vs. Ag + /Ag) for 5 h. XRD analysis shows that Li 2 O is not electrochemically reduced to Li at −1.0 V (vs. Ag + /Ag) or more negative potential. During the preparation process of Al–Cu–Li alloy, lithium peroxide is formed as an intermediate compound. Al–Cu–Li alloy is chemically prepared through the reaction between aluminum and lithium peroxide by heating of Al–Cu–Li 2 O precursors in KCl–LiCl–LiF melt at 1023 K. Eelectro-deoxidation in LiCl–KCl melt can increase the lithium content in the final alloy product. Al–Mg and Al–Nd alloy were also prepared by using the same method from their mixture of aluminum and corresponding oxide, respectively. Al–Nd alloy can only be obtained at the temperature above 773 K. Al–Li alloy could not be obtained in eutectic CaCl 2 –LiCl melt because of formation of calcium aluminates. - Highlights: • Al–Cu–Li alloy was prepared using electrochemical deoxidation of Al–Cu–Li 2 O precursor in eutectic KCl–LiCl melt at 648 K. • Al–Nd alloy was successfully produced by the same method at 773 K. • CaCl 2 –LiCl melt is not a good choice for preparing Al–Li alloy because of formation of calcium aluminate.

Direct preparation of Al-base alloys from their oxides/metal precursors in the eutectic LiCl–KCl melt

Energy Technology Data Exchange (ETDEWEB)

Gao, Bingliang, E-mail: blgao@mail.neu.edu.cn; Zhu, Hao; Xia, Yuxiang; Shi, Zhongning; Hu, Xianwei; Wang, Zhaowen

2016-04-25

A study was carried out on the preparation of Al–Cu–Li alloy from their oxides/metal precursors using the method of electro-deoxidation in the eutectic LiCl–KCl melt at 648 K. Cyclic voltammetry was used to characterize the system. The samples were prepared by potentiostatic electrolysis at −1.0 V to −2.0 V (vs. Ag{sup +}/Ag) for 5 h. XRD analysis shows that Li{sub 2}O is not electrochemically reduced to Li at −1.0 V (vs. Ag{sup +}/Ag) or more negative potential. During the preparation process of Al–Cu–Li alloy, lithium peroxide is formed as an intermediate compound. Al–Cu–Li alloy is chemically prepared through the reaction between aluminum and lithium peroxide by heating of Al–Cu–Li{sub 2}O precursors in KCl–LiCl–LiF melt at 1023 K. Eelectro-deoxidation in LiCl–KCl melt can increase the lithium content in the final alloy product. Al–Mg and Al–Nd alloy were also prepared by using the same method from their mixture of aluminum and corresponding oxide, respectively. Al–Nd alloy can only be obtained at the temperature above 773 K. Al–Li alloy could not be obtained in eutectic CaCl{sub 2}–LiCl melt because of formation of calcium aluminates. - Highlights: • Al–Cu–Li alloy was prepared using electrochemical deoxidation of Al–Cu–Li{sub 2}O precursor in eutectic KCl–LiCl melt at 648 K. • Al–Nd alloy was successfully produced by the same method at 773 K. • CaCl{sub 2}–LiCl melt is not a good choice for preparing Al–Li alloy because of formation of calcium aluminate.

Investigation of the yield process by deformation luminescence of X-ray irradiated KCl:Ca2+

International Nuclear Information System (INIS)

Nakamura, S.; Ida, K.; Ohgaku, T.

2011-01-01

It is found that deformation luminescence gives us information about the microscopic yield process of X-ray irradiated KCl:Ca 2+ . The stress-strain curve has a macroscopic yield point. But we find that luminescence appears to start before the macroscopic yield. This means that dislocation begin to move before the macroscopic yield because deformation luminescence is attributed to radiation-induced dislocation motion. The beginning of luminescence is considered to be the microscopic yield. Investigating the dependence of microscopic yield stress on strain rate and impurity concentration gives us additional information. The activation volume obtained from the dependence of microscopic yield stress on strain rate is comparable to the value estimated from the concentration of impurity. Then the dislocation starts to move overcoming impurity-vacancy dipoles as obstacles to dislocation motion. The dislocation density starts to increase at the microscopic yield point and then sharply increases to the macroscopic yield.

Electrochemical preparation of Al–Sm intermetallic compound whisker in LiCl–KCl Eutectic Melts

International Nuclear Information System (INIS)

Ji, De−Bin; Yan, Yong−De; Zhang, Mi−Lin; Li, Xing; Jing, Xiao−Yan; Han, Wei; Xue, Yun; Zhang, Zhi−Jian; Hartmann, Thomas

2015-01-01

Highlights: • The reduction process of Sm(III) was investigated in LiCl–KCl melt on an aluminum electrode at 773 K. • Al–Sm alloy with different phase structure (Al 2 Sm and Al 3 Sm) was prepared by potentiostatic electrolysis on an aluminum electrode with the change of electrolytic potentials and time in LiCl–KCl–SmCl 3 melts. • Al − Sm alloy containing whiskers (Al 4 Sm) was obtained by potentiostatic electrolysis (−2.10 V) on an aluminum electrode for 7 hours with the change of electrolytic temperature and cooling rate in LiCl–KCl–SmCl 3 (16.5 wt. %) melts. The results from micro–hardness test and potentiodynamic polarization test show the micro hardness and corrosion property are remarkably improved with the help of Al–Sm intermetallic compound whiskers. - Abstract: This work presents the electrochemical study of Sm(III) on an aluminum electrode in LiCl–KCl melts at 773 K by different electrochemical methods. Three electrochemical signals in cyclic voltammetry, square wave voltammetry, open circuit chronopotentiometry, and cathode polarization curve are attributed to different kinds of Al–Sm intermetallic compounds, Al 2 Sm, Al 3 Sm, and Al 4 Sm, respectively. Al–Sm alloy with different phase structure (Al 2 Sm and Al 3 Sm) could be obtained by the potentiostatic electrolysis with the change of electrolytic potentials and time. Al–Sm alloy containing whiskers (Al 4 Sm) was obtained by potentiostatic electrolysis (−2.10 V) on an aluminum electrode for 7 hours with the change of electrolytic temperature and cooling rate in LiCl–KCl–SmCl 3 (16.5 wt. %) melts. The XRD and SEM&EDS were employed to investigate the phase composition and microstructure of Al–Sm alloy. SEM analysis shows that lots of needle−like precipitates formed in Al–Sm alloy, and their ratios of length to diameter are found to be greater than 10 to 1. The TEM and electron diffraction pattern were performed to investigate the crystal structure of the

Comparative study of the thermoluminescence between the materials {alpha}-Al{sub 2}O{sub 3}:C, KCl:Eu{sup 2+}, KBr: Eu{sup 2+} and VYCOR; Estudio comparativo de la termoluminiscencia entre los materiales {alpha}-Al{sub 2}O{sub 3}: C, KCl:Eu{sup 2+}, KBr: Eu{sup 2+} y VYCOR

Energy Technology Data Exchange (ETDEWEB)

Pedroza M, M. [Programa de Posgrado en Fisica de Materiales, Centro de Investigacion Cientifica y de Educacion Superior de Ensenada, Apdo. Postal 2681, C.P. 22800, Ensenada, Baja California (Mexico); Melendrez, R.; Perez S, R.; Aceves, R.; Piters, T.M.; Barboza F, M. [Centro de Investigacion en Fisica, Universidad de Sonora, Apdo. Postal 5-088, C.P. 83190 Hermosillo, Sonora (Mexico)

1999-07-01

It is presented some investigation results related to the thermoluminescence curves (Tl), Tl emission and the spectra of excitation of thermoluminescence in the ultraviolet region of 190 to 250 nm in the materials {alpha}-Al{sub 2}O{sub 3}:C, KCl: Eu{sup 2+}, KBr: Eu{sup 2+} and the Vycor glass. It was able to be observed that the Tl emission for the first three materials exists around 420 nm and in the case of Vycor the emission consists of two Tl peaks where the most low temperature is a band more wide centered in 460 nm and the other band of high temperature emits in 470 nm. In the excitation curves of Tl were obtained centered bands around 230 nm for KCl: Eu{sup 2+}, 235 nm for KBr: Eu{sup 2+}, 220 nm for the alumina and 195 nm for the Vycor. From the results it was able to be appreciated that this last has a minor relative intensity with respect to the others materials but also the region in which works there was an alone band between the 190 to 205 nm. This fact makes the material be very selective in the ultraviolet region of greatest energy. (Author)

The effect of mixed HCl–KCl competitive adsorbate on Pt adsorption and catalytic properties of Pt–Sn/Al{sub 2}O{sub 3} catalysts in propane dehydrogenation

Energy Technology Data Exchange (ETDEWEB)

Zangeneh, Farnaz Tahriri, E-mail: tahriri_zangeneh@yahoo.com [Department of Chemistry, Science and Research Branch, Islamic Azad University, P.O. Box 14155-4933, Tehran (Iran, Islamic Republic of); Catalyst Research Group, Petrochemical Research and Technology Company, National Petrochemical Company, P.O. Box 14358-84711, Tehran (Iran, Islamic Republic of); Taeb, Abbas [Department of Chemistry, Science and Research Branch, Islamic Azad University, P.O. Box 14155-4933, Tehran (Iran, Islamic Republic of); Gholivand, Khodayar [Department of Chemistry, Faculty of Sciences, Tarbiat Modares University, P.O. Box 14115-175, Tehran (Iran, Islamic Republic of); Sahebdelfar, Saeed [Catalyst Research Group, Petrochemical Research and Technology Company, National Petrochemical Company, P.O. Box 14358-84711, Tehran (Iran, Islamic Republic of)

2015-12-01

Highlights: • Impregnation is a critical step in preparation of Pt-based dehydrogenation catalysts. • A competitor ion could strongly influence the impregnation of Pt on alumina support. • The competitor type is much more effective than pH of impregnation solution. • HCl competitor can be partially replaced by KCl reducing acidic attack on support. • Adsorption parameters can be estimated by a simple equilibrium-based model. - Abstract: The effect of competitive adsorbate concentration and combination on the adsorption of H{sub 2}PtCl{sub 6} onto γ-Al{sub 2}O{sub 3} in the preparation and performance of PtSnK/γ-Al{sub 2}O{sub 3} catalyst for propane dehydrogenation was investigated. The catalysts were prepared by sequential impregnation of Sn and Pt precursors. The effect of competitor concentration on Pt adsorption was studied by using hydrochloric acid (0.1–0.3 M) and the effect of pH was studied by using KCl/HCl mixtures at constant (0.1 M) total chloride ion concentration. The catalysts were characterized by nitrogen adsorption/desorption, XRD, XRF, SEM and CO chemisorption. The catalytic performance tests were carried out in a fixed-bed quartz reactor under kinetic controlled condition for proper catalyst screening. It was found that the corrosive competitor HCl could be partially substituted with KCl without appreciable impact on catalyst performance with the advantage of lower acid attack on the support and reduced leaching of the deposited tin. A model based on initial concentration and uptake of the adsorbates was developed to obtain the adsorption parameters. Values of 890 μmol/g and 600 lit/mol were obtained for adsorption site concentration of the tin-impregnated support and equilibrium constant for Pt adsorption, respectively, for HCl concentration range of 0.1–0.3 M.

ROS activate KCl cotransport in nonadherent Ehrlich ascites cells but K⁺ and Cl^- channels in adherent Ehrlich Lettré and NIH3T3 cells

DEFF Research Database (Denmark)

Lambert, Ian Henry; Klausen, Thomas Kjær; Bergdahl, Andreas

2009-01-01

Addition of H2O2 (0.5 mM) to Ehrlich ascites tumor cells under isotonic conditions results within 25 min in a substantial (22 +/- 1 %) reduction in cell volume. The cell shrinkage is paralleled by net loss of K(+), which was significant within 8 min, whereas no concomitant increase in the K......(+) or Cl(-) conductances could be observed. The H2O2-induced cell shrinkage was unaffected by the presence of clofilium and clotrimazole, that block volume-sensitive and Ca(2+)-activated K(+) channels, respectively, and unaffected by a raise in extracellular K(+) concentration to a value which eliminates...... the electrochemical driving force for K(+). On the other hand, the H2O2-induced cell shrinkage was impaired in the presence of the KCl cotransport inhibitor DIOA, following substitution of NO3(-) for Cl(-), and when the driving force for KCl cotransport was omitted. It is suggested that H2O2 activates electro neutral...

Pengaruh Pemberian Urea, Tsp, Kcl Dan Pupuk Organik Cair (Poc) Kulit Pisang Terhadap Pertumbuhan Dan Produksi Tanaman Cabai Merah Keriting (Capsicum Annum L.)

OpenAIRE

adrian, Edo; Yetti, Husna

2017-01-01

This research to determine the interaction of inorganic fertilizer (Urea, TSP, KCl)and banana peelliquid organic fertilizer (POC) to find the best results on the growth and yield of red pepper (Capsicum annuum L.).This study was conducted for four months (March-June, 2016), the Experimental Station, Faculty of Agriculture, University of Riau Pekanbaru,using a completely randomized design (CRD) factorial,consists of two factors and three replications.The results were analyzed by analysis of va...

Formation and control of zinc nitride in a molten LiCl-KCl-Li3N system

International Nuclear Information System (INIS)

Goto, Takuya; Toyoura, Kazuaki; Tsujimura, Hiroyuki; Ito, Yasuhiko

2004-01-01

We investigated a possibility of electrochemical formation and control of zinc nitride in a molten LiCl-KCl-Li 3 N system at 673 K. Zinc nitride films were obtained by means of potentiostatic electrolysis of zinc electrodes in the melt. From XRD analysis, it was confirmed that obtained films consisted of Zn 3 N 2 and LiZnN and that the composition of each film was effected by the applied potential value. In the potential range from 0.75 to 1.6 V (versus Li + /Li), the ratio of Zn 3 N 2 increased as the applied potential was more positive. Based on the result, we achieved the formation of Zn 3 N 2 film (3-5 μm) in anti-scandium oxide structure (a = 0.977 nm) by means of potentiostatic electrolysis at 1.6 V for 3 h

The effect of various electrolyte cations on electrochemical performance of polypyrrole/RGO based supercapacitors.

Science.gov (United States)

Zhu, Jianbo; Xu, Youlong; Wang, Jie; Lin, Jun; Sun, Xiaofei; Mao, Shengchun

2015-11-21

In this work, polypyrrole/graphene doped by p-toluenesulfonic is prepared as an active material for supercapacitors, and its capacitance performance is investigated in various aqueous electrolytes including HCl, LiCl, NaCl, and KCl with a concentration of 3 M, respectively. A rising trend of capacitance is observed according to the cationic mobility (Li(+) Na(+) > Li(+) > H(+)). The reason can be attributed to the fact that the insertion/de-insertion of large size cation brings a significant doping level decrease and an over-oxidation increase during the charging-discharging cycles. Hence, we not only obtain good capacitance performance (280.3 F g(-1) at 5 mV s(-1)), superior rate capability (225.8 F g(-1) at 500 mV s(-1)) and high cycling stability (92.0% capacitance retention after 10,000 cycles at 1 A g(-1)) by employing 3 M HCl as an electrolyte, but also reveal that the electrolyte cations have a significant effect on the supercapacitors' electrochemical performance.

Pyrometallurgical separation processes of radionuclides contained in the irradiated nuclear fuel

International Nuclear Information System (INIS)

De Cordoba, Guadalupe; Caravaca, Concha; Quinones, Javier; Gonzalez de la Huebra, Angel

2005-01-01

Faced with the new options for the high level waste management, the ''Partitioning and Transmutation (P and T)'' of the radio nuclides contained in the irradiated nuclear fuel appear as a promising option from different points of view, such as environmental risk, radiotoxic inventory reduction, economic, etc.. The present work is part of a research project called ''PYROREP'' of the 5th FWP of the EU that studied the feasibility of the actinide separation from the rest of fission products contained in the irradiated nuclear fuel by pyrometallurgical processes with the aim of their transmutation. In order to design these processes it is necessary to determine basic thermodynamic and kinetic data of the radionuclides contained in the nuclear fuel in molten salt media. The electrochemical study of uranium, samarium and molybdenum in the eutectic melt LiCl - KCl has been performed at a tungsten electrode in the temperature range of 450 - 600 deg C in order to obtain these basic properties. (Author)

Theoretical and experimental studies of reverse osmosis separation of inorganic salts in aqueous solutions; Estudio teorico y experimental de parametros de transporte a traves de membranas de osmosis inversa : Efecto de varios tipos de sales

Energy Technology Data Exchange (ETDEWEB)

Khavet, M.; Mengual, J. I.

2004-07-01

Theoretical and experimental studies of reverse osmosis separation of inorganic salts in aqueous solutions have been carried out. In this study, a polyamide thin film composite membrane in spiral wound configuration was used. The free energy of different inorganic monovalent (LiCl, NaCl, KCl, NaBr, NaI, LiBr, KBr) and divalent (MgCl2, MnCl2, CaCl2, MgBr2) salts has been calculated. The solute transport parameters were related to the free energy of the corresponding cations and anions. The mass transfer coefficient at the high pressure feed side of the spiral wound module was determined for each type of salt. The obtained theoretical values were compared to the experimental ones. The good agreements observed between the experimental and theoretical results confirm the validity of the theoretical procedure, which may be applied in modelling solar reverse osmosis plants for the prediction of the separation factor of various types of inorganic salts. (Author)

Melting of KCl and pressure calibration from in situ ionic conductivity measurements in a multi-anvil apparatus

Science.gov (United States)

Li, J.; Dong, J.; Zhu, F.

2017-12-01

Melting plays an unparalleled role in planetary differentiation processes including the formation of metallic cores, basaltic crusts, and atmospheres. Knowledge of the melting behavior of Earth materials provides critical constraints for establishing the Earth's thermal structure, interpreting regional seismic anomalies, and understanding the nature of chemical heterogeneity. Measuring the melting points of compressed materials, however, have remained challenging mainly because melts are often mobile and reactive, and temperature and pressure gradients across millimeter or micron-sized samples introduce large uncertainties in melting detection. Here the melting curve of KCl was determined through in situ ionic conductivity measurements, using the multi-anvil apparatus at the University of Michigan. The method improves upon the symmetric configuration that was used recently for studying the melting behaviors of NaCl, Na2CO3, and CaCO3 (Li and Li 2015 American Mineralogist, Li et al. 2017 Earth and Planetary Science Letters). In the new configuration, the thermocouple and electrodes are placed together with the sample at the center of a cylindrical heater where the temperature is the highest along the axis, in order to minimize uncertainties in temperature measurements and increase the stability of the sample and electrodes. With 1% reproducibility in melting point determination at pressures up to 20 GPa, this method allows us to determine the sample pressure to oil load relationship at high temperatures during multiple heating and cooling cycles, on the basis of the well-known melting curves of ionic compounds. This approach enables more reliable pressure measurements than relying on a small number of fixed-point phase transitions. The new data on KCl bridge the gap between the piston-cylinder results up to 4 GPa (Pistorius 1965 J. of Physics and Chemistry of Solids) and several diamond-anvil cell data points above 20 GPa (Boehler et al. 1996 Physical Review). We

In vitro protective efficacy of Lithium chloride against Mycoplasma hyopneumoniae infection.

Science.gov (United States)

Ishag, Hassan Z A; Wu, Yu-Zi; Liu, Mao-Jun; Xiong, Qi-Yan; Feng, Zhi-Xin; Yang, Ruo-Song; Shao, Guo-Qing

2016-06-01

Mycoplasma hyopneumoniae (M. hyopneumoniae) infection affects the swine industry. Lithium chloride (LiCl), is a drug used to treat bipolar disorder and has also shown activity against bacterial and viral infections. Herein, we evaluated the antibacterial activity of LiCl on PK-15 cells infected with M. hyopneumoniae. Incubation of LiCl (40mM) with cells for 24h, did not significantly affect the cell viability. The qRT-PCR showed ~80% reduction in M. hyopneumoniae genome when LiCl added post-infection. A direct effect of LiCl on bacteria was also observed. However, treatment of cells with LiCl prior infection, does not protect against the infection. Anti-bacterial activity of LiCl was further confirmed by IFA, which demonstrated a reduction in the bacterial protein. With 40mM LiCI, the apoptotic cell death, production of nitric oxide and superoxide anion induced by M. hyopneumoniae, were prevented by ~80%, 60% and 58% respectively. Moreover, caspase-3 activity was also reduced (82%) in cells treated with 40mM LiCl. LiCl showed activity against various strains of M. hyopneumoniae examined in our study. Collectively, our data showed that LiCl inhibited the infection of M. hyopneumoniae through anti-apoptotic mechanism. Copyright © 2016 Elsevier Ltd. All rights reserved.

Magneto-optical measurement of spin-lattice relaxation time in KBr and in the Na and Cs halogenetes and Co++ ion magnetic circular dichroism study in KCl

International Nuclear Information System (INIS)

Carvalho, R.A.

1977-01-01

A magnetic circular dicroism spectrometer is described, which was used in the following experiments: 1) The spin-lattice relaxation time (T 1 ) for F centers in NaCl, NaBr, CsBr and CsCl, at 1,8 0 K in magnetic fields up to 15000Gs is described. The suitability of the theory of ref. (08) to explain the differences observed for halides of differents alkali ions as well as for different structures is verified proves that the hyperfine interaction is the most important mechanism for this kind of centers. It is also verified that, for temperatures between 6 0 K and 15 0 K, T 1 experimental values fits the theory of ref. (21) reasonably well, for F centers in KBr. This theory us an extension of that of ref. (8). 2) The MCD spectra for KCl:Co ++ and Caf 2 :Co ++ in different magnetic fields up to 56KGs, and in temperature range between 1,8 0 K and 4,2 0 K is obtained. The results are consistent with the assumption that Co ++ centers are intersticial in KCl lattice [pt

Thermally and optically stimulated luminescence correlated processes in X-ray irradiated KCl:Eu2+

International Nuclear Information System (INIS)

Chernov, V.; Melendrez Ao, R.; Piters, T.M.; Barboza-Flores, M.

2001-01-01

The effect of optical bleaching on thermoluminescence (TL) and thermal bleaching on optically stimulated luminescence (OSL) outputs in X-ray irradiated KCl : Eu 2+ have been investigated. The X-ray induced glow curves reveal three main peaks located at 370, 410 and 470 K. Illumination with 560 nm light leads to a drastic change of the TL glow curve. The 470 K peak is destroyed during bleaching. The other peaks initially increase in intensity and only after sufficiently long bleaching begin to decrease. After long-time bleaching, the TL peaks in X-ray irradiated crystals look like the TL peaks found in UV irradiated crystals. The effect of thermal bleaching on OSL is also very pronounced. The temperature dependencies show a step-by-step decrease of the OSL intensity correlated with the positions of the TL peaks. The result obtained shows that centers responsible for the TL peaks participate in OSL, but this participation seems not to be direct and is complicated by processes accompanying the F center bleaching

On the nature of absorption in the range of CO2-laser radiation and laser-induced destruction of KCl crystals at the first stage of radiation colouring

International Nuclear Information System (INIS)

Gektin, A.V.; Charkina, T.A.; Shiran, N.V.

1985-01-01

A mechanism explaining both an increase of crystal absorption in CO 2 -laser radiation range and a decrease of the thershold of KCl crystals optical destruction is proposed. The mechanism is based on the presence of a bond between hydroxyl ion content and a change of crystal transparency in the IR range under γ-radiation at the first stage of radiation colouring

Isopiestic determination of the osmotic and activity coefficients of the {yKCl + (1 - y)K2HPO4}(aq) system at T = 298.15 K

International Nuclear Information System (INIS)

Popovic, Daniela Z.; Miladinovic, Jelena; Todorovic, Milica D.; Zrilic, Milorad M.; Rard, Joseph A.

2011-01-01

Highlights: → Isopiestic measurements were made for {yKCl + (1 - y)K 2 HPO 4 }(aq) at T = 298.15 K. → The resulting osmotic coefficients were represented by three thermodynamic models. → Activity coefficients from Pitzer model with Scatchard mixing terms are recommended. - Abstract: The osmotic coefficients of aqueous mixtures of KCl and K 2 HPO 4 have been measured at T = (298.15 ± 0.01) K by the isopiestic vapor pressure method over the range of ionic strengths from (2.3700 to 11.250) mol . kg -1 using CaCl 2 (aq) as the reference solution. Our new experimental results were modeled with an extended form of Pitzer's ion-interaction model equations, both with the usual mixing terms and with Scatchard's neutral-electrolyte mixing terms, and with the Clegg-Pitzer-Brimblecombe equations based on the mole-fraction-composition scale. There is a dearth of previously published isopiestic data for mixtures containing salts of HPO 4 2- (aq) and, consequently, no previous measurements are available for comparison with the present results. The present study yields Cl - HPO 4 2- mixing parameters for these three models that are needed for modeling the thermodynamic activities of solute components of natural waters and other complex aqueous electrolyte mixtures.

First principles study of the thermodynamic and kinetic properties of U in an electrorefining system using molybdenum cathode and LiCl-KCl eutectic molten salt

International Nuclear Information System (INIS)

Kwon, Choah; Kang, Joonhee; Kang, Woojong; Kwak, Dohyun; Han, Byungchan

2016-01-01

Using first principles density functional theory (DFT) calculations we obtain thermodynamic and kinetic properties of U in an electrorefining process for spent nuclear fuels using a LiCl-KCl eutectic molten salt and Mo as a cathode. The thermodynamic stability of electrodeposited U from the molten salt onto the Mo(110) surface electrode is evaluated by activity coefficients as function of surface coverages of U and Cl. Additionally, ab-initio molecular dynamic simulations combined with the Stokes-Einstein-Sutherland relation enables us to calculate the viscosity of the LiCl-KCl eutectic molten salt. Our results well agree with previously reported experimental data endorsing the credibility. Based on our atomic-level mechanical understanding we propose that an accurate computational model system incorporating the electrochemical conditions of the electrorefining process essential for the purpose of establishing thermodynamic and kinetic database of U, otherwise critical deviations are inevitable. More interestingly, the effect of coadsorption of Cl with U on the Mo(110) surface plays a key role in stabilizing electrodeposited U on the cathode. Our approach can be useful for validating published experimental database and for identifying key factors guiding a rational design of highly efficient electrorefining system for spent nuclear fuels, and thus reducing high-level radioactive nuclear wastes.

Influence of oxide and alloy formation on the Electrochemistry of Ti deposition from the NaCl-KCl-NaF-K-2 TiF6 melt reduced by metallic Ti

DEFF Research Database (Denmark)

Barner, Jens H. Von; Precht Noyé, Pernille; Barhoun, A

2005-01-01

The redox reactions in KCl-NaCl-NaF-K2TiF6 melts reduced by titanium metal have been studied by cyclic voltammetry and chronopotentiommetry. At platinum and nickel electrodes waves due to alloy formation were seen preceding the Ti(III) --> Ti metal deposition wave. The presence of oxide species...

Thermoluminescence dependence on the wavelength of monochromatic UV-radiation in Cu-doped KCl and KBr at room temperature

Energy Technology Data Exchange (ETDEWEB)

Perez R, A.; Piters, T.; Aceves, R.; Rodriguez M, R.; Perez S, R., E-mail: rperez@cifus.uson.mx [Universidad de Sonora, Departamento de Investigaciones en Fisica, Apdo. Postal 5-088, 83190 Hermosillo, Sonora (Mexico)

2014-08-15

Thermoluminescence (Tl) dependence on the UV irradiation wavelengths from 200 to 500 nm in Cu-doped KCl and KBr crystals with different thermal treatment has been analyzed. Spectrum of the Tl intensity of each material show lower intensity at wavelengths longer than 420 nm. The Tl intensity depends on the irradiation wavelength. Structure of the Tl intensity spectrum of each sample is very similar to the structure of its optical absorption spectrum, indicating that at each wavelength, monochromatic radiation is absorbed to produce electronic transitions and electron hole pairs. Thermoluminescence of materials with thermal treatment at high temperature shows electron-hole trapping with less efficiency. The results show that Cu-doped alkali-halide materials are good detectors of a wide range of UV monochromatic radiations and could be used to measure UV radiation doses. (Author)

Thermoluminescence dependence on the wavelength of monochromatic UV-radiation in Cu-doped KCl and KBr at room temperature

International Nuclear Information System (INIS)

Perez R, A.; Piters, T.; Aceves, R.; Rodriguez M, R.; Perez S, R.

2014-08-01

Thermoluminescence (Tl) dependence on the UV irradiation wavelengths from 200 to 500 nm in Cu-doped KCl and KBr crystals with different thermal treatment has been analyzed. Spectrum of the Tl intensity of each material show lower intensity at wavelengths longer than 420 nm. The Tl intensity depends on the irradiation wavelength. Structure of the Tl intensity spectrum of each sample is very similar to the structure of its optical absorption spectrum, indicating that at each wavelength, monochromatic radiation is absorbed to produce electronic transitions and electron hole pairs. Thermoluminescence of materials with thermal treatment at high temperature shows electron-hole trapping with less efficiency. The results show that Cu-doped alkali-halide materials are good detectors of a wide range of UV monochromatic radiations and could be used to measure UV radiation doses. (Author)

Thermally stimulated luminescence of mixed sintered KCl-KBr: EuCl3 pellets exposed to gamma rays

International Nuclear Information System (INIS)

Cervantes, B.; Bernal, R.; Barboza F, M.; Cruz V, C.; Burruel I, S.E.; Cruz Z, E.

2006-01-01

Europium-doped pellets of mixed composition type KCI x Br 1-x : EuCl 3 were obtained by sintering. Some of these polycrystalline samples were exposed to cobalt-60 gamma rays at 0.56 Gy/min dose rate. The higher TL efficiencies were observed for that phosphors with higher concentration of KCI ions in the composition lattice. The integrated TL as a function of dose were investigated in the 0.25-150 Gy dose range and it showed an increase when increasing dose, and a close linear behavior for the lower doses. Mixed composition samples have a reproducibility of the TL signals better than the end compositions KBr: EuCI 3 and KCl: EuCI 3 . The characteristic fading depends strongly on the relative composition. The kinetics parameters were calculated by the Initial Rise method and showed an important increase of the values of the activation energy with the absorption dose increased. (Author)

Electrochemical extraction of neodymium by co-reduction with aluminum in LiCl–KCl molten salt

International Nuclear Information System (INIS)

Yan, Yong-De; Xu, Yan-Lu; Zhang, Mi-Lin; Xue, Yun; Han, Wei; Huang, Ying; Chen, Qiong; Zhang, Zhi-Jian

2013-01-01

The electrochemical behavior of Nd(III) ions in LiCl–KCl and LiCl–KCl–AlCl 3 melts on a Mo electrode at 723 K was studied by various electrochemical techniques. The results showed that Nd(III) ions are reduced to Nd(0) through two consecutive steps, and the underpotential deposition of neodymium on pre-deposited Al electrode formed two kinds of Al–Nd intermetallic compounds in LiCl–KCl–AlCl 3 solutions. The electrochemical extraction of neodymium was carried out in LiCl–KCl–AlCl 3 melts on a Mo electrode at 873 K by potentiostatic and galvanostatic electrolysis. The extraction efficiency was 99.25% after potentiostatic electrolysis for 30 h. Al–Li–Nd bulk alloy was obtained by galvanostatic electrolysis. X-ray diffraction (XRD) suggested that Al 2 Nd and Al 3 Nd phases were formed in Al–Li–Nd alloy. The microstructure and micro-zone chemical analysis of Al–Li–Nd alloy were characterized by scanning electron microscopy (SEM) with energy dispersive spectrometry (EDS), respectively

Combinatorial treatment with lithium chloride enhances recombinant antibody production in transiently transfected CHO and HEK293E cells

DEFF Research Database (Denmark)

Kim, Che Lin; Kwang Ha, Tae; Min Lee, Gyun

2016-01-01

Lithium chloride (LiCl), which induces cell cycle arrest at G2/M phase, is known as a specific production rate (qp)-enhancing additive in recombinant Chinese hamster ovary (CHO) cell culture. To determine the potential of LiCl as a chemical additive that enhances transient gene expression (TGE), Li......Cl was added to the CHO-NK and human embryonic kidney 293E (HEK293E) cell cultures before and/or after transfection with polyethylenimine as a transfection reagent. The effect of this addition on transfection efficiency (pre-treatment) and qp enhancement during TGE (post-treatment) was examined. For the TGE...... of monoclonal antibody (mAb) in CHO-NK cells, pretreatment alone with 10 mM LiCl and post-treatment alone with 5 mM LiCl resulted in 1.2- and 3.4-fold increase of maximum mAb concentration (MMC), respectively, compared with the TGE without LiCl treatment. Furthermore, combinatorial treatment with LiCl (10 m...

Formation and control of zinc nitride in a molten LiCl-KCl-Li{sub 3}N system

Energy Technology Data Exchange (ETDEWEB)

Goto, Takuya; Toyoura, Kazuaki; Tsujimura, Hiroyuki; Ito, Yasuhiko

2004-08-25

We investigated a possibility of electrochemical formation and control of zinc nitride in a molten LiCl-KCl-Li{sub 3}N system at 673 K. Zinc nitride films were obtained by means of potentiostatic electrolysis of zinc electrodes in the melt. From XRD analysis, it was confirmed that obtained films consisted of Zn{sub 3}N{sub 2} and LiZnN and that the composition of each film was effected by the applied potential value. In the potential range from 0.75 to 1.6 V (versus Li{sup +}/Li), the ratio of Zn{sub 3}N{sub 2} increased as the applied potential was more positive. Based on the result, we achieved the formation of Zn{sub 3}N{sub 2} film (3-5 {mu}m) in anti-scandium oxide structure (a = 0.977 nm) by means of potentiostatic electrolysis at 1.6 V for 3 h.

Experimental study of formation and dynamics of cavitation bubbles and acoustic flows in NaCl, KCl water solutions

Science.gov (United States)

Rybkin, K. A.; Bratukhin, Yu. K.; Lyubimova, T. P.; Fatallov, O.; Filippov, L. O.

2017-07-01

The acoustic flows and the phenomena associated with them arising under the action of ultrasound of different power on distilled water and aqueous solutions of a mixture of NaCl and KCl salts of various concentrations are studied experimentally. It is found that in the distilled water, under the action of ultrasound, the appearance of inertial and non-inertial cavitation bubbles takes place, then the formation of stable clusters, the distance between which depends on the power of the ultrasound source is observed. Experiments show that an increase in the mass concentration of salts in water leads to the decrease in the average diameter of the arising inertial cavitation bubbles and to the gradual decrease in their number, up to an almost complete disappearance at nearly 13% of the concentration of the salt mixture in the water.

Noise as a Public Health Problem: Proceedings of the International Congress (4th) Held at Turin (Italy) on June 21-25, 1983. Volume 1.

Science.gov (United States)

1983-11-01

which it is the constant, albeit unwelcome companion . Rapid, tempestuous industrialisation in Italy, particularly since the war, has quickly raised the...Mandaliev, A., 1973. Issledovanie vlijanija suma na sluhoroi apparat arterialnoe davlenic i nervruja sistema rabocih tekstilnoi promyslennosti

Evaluation of interatomic potentials for rainbow scattering under axial channeling at KCl(0 0 1) surface by three-dimensional computer simulations based on binary collision approximation

Energy Technology Data Exchange (ETDEWEB)

Takeuchi, Wataru, E-mail: take@sp.ous.ac.jp

2017-05-01

The rainbow angles corresponding to prominent peaks in the angular distributions of scattered projectiles with small angle, attributed to rainbow scattering (RS), under axial surface channeling conditions are strongly influenced by the interatomic potentials between projectiles and target atoms. The dependence of rainbow angles on normal energy of projectile energy to the target surface, being experimentally obtained by Specht et al. for RS of He, N, Ne and Ar atoms under 〈1 0 0〉 and 〈1 1 0〉 axial channeling conditions at a KCl(0 0 1) surface with projectile energies of 1–60 keV, was evaluated by the three-dimensional computer simulations using the ACOCT code based on the binary collision approximation with interatomic pair potentials. Good agreement between the ACOCT results using the ZBL pair potential and the individual pair potentials calculated from Hartree-Fock (HF) wave functions and the experimental ones was found for RS of He, N and Ne atoms from the atomic rows along 〈1 0 0〉 direction. For 〈1 1 0〉 direction, the ACOCT results employing the Moliere pair potential with adjustable screening length of O’Connor-Biersack (OB) formula, the ZBL pair potential and the individual HF pair potentials except for Ar → KCl using the OB pair potential are nearly in agreement with the experimental ones.

Lithium Chloride Modulates Adipogenesis and Osteogenesis of Human Bone Marrow-Derived Mesenchymal Stem Cells

Directory of Open Access Journals (Sweden)

Linjun Tang

2015-08-01

Full Text Available Background/Aims: Lithium chloride (LiCl has long been used as a psychiatric medication; however, its role in the differentiation of bone marrow-derived mesenchymal stem cells (BMSCs remains largely unknown. The aim of this study is to explore the effect of LiCl on the differentiation of BMSCs. Methods: The roles of LiCl in osteogenic and adipogenic processes were observed using alizarin red staining and oil red O staining, respectively. The effects of LiCl on the Wnt and Hedgehog (Hh pathways were investigated. Results: Our data showed that LiCl effectively promoted osteogenesis and inhibited adipogenesis by simultaneously affecting the Wnt and Hh pathways. Conclusion: These results suggest that LiCl influences the differentiation of BMSCs directly through the Wnt and Hh pathways and thus may be a candidate drug for the treatment of osteoporosis.

Tunneling-recombination luminescence between Ag0 and Ag2+ in KCl:AgCl

International Nuclear Information System (INIS)

Delbecq, C.J.; Dexter, D.L.; Yuster, P.H.

1978-01-01

Appropriate treatment of a KCl:AgCl crystal results in the trapping of electrons as silver atoms, Ag 0 , and positive holes as AgCl 4 2- , Ag 2+ , centers. Optical excitation of Ag 0 in such a crystal at T 0 and Ag 2+ pairs, similar to the Ag 0 -Cl 2 - tunneling-recombination studies we previously reported. We have shown that Ag 2+ centers are involved in the emission process by preferentially orienting the anisotropic Ag 2+ at 6 K by excitation with polarized light and observing that the afterglow is polarized. Upon warming to 50 K, where the preferentially oriented Ag 2+ can change orientation, a strong reversal in the degree of polarization occurs which finally decays to zero. The characteristics of this luminescence can be understood if we assume: (i) a tunneling-recombination mechanism in which the orientation of the electric vector of the emitted radiation depends on the position of the Ag 0 relative to the Ag 2+ and (ii) the tunneling is anisotropic and depends on the location of the Ag 0 relative to the anisotropic Ag 2+ . The latter assumption is based on the tetragonal (d-like) symmetry of the Ag 2+ complex. Good quantitative agreement between theory and experiment has been obtained on the decay kinetics, the degree of polarization, and the polarization reversal

On chlorization of uranium and plutonium oxides in NaCl-KCl-MgCl2 molten eutectic

International Nuclear Information System (INIS)

Vorobej, M.P.; Desyatnik, V.N.; Pirogov, S.M.

1978-01-01

The chlorination process of U 3 O 8 , UO 2 , and PuO 2 in a melt of anhydrous NaCl-KCl-MgCl 2 with gaseous chlorine and carbon tetrachloride has been studied. The chlorination rate of uranium oxides has been studied within a temperature range 500-800 deg C at a chlorine feeding rate of 10 ml/min. Thermoqravimetric and X-ray analyses have shown that K 2 UO 2 Cl 4 compound is the final product of chlorination of uranium oxides. The mechanism of chlorination has been proposed. THe rate of PuO 2 chlorination has been studied within the same temperature range. It has been established that PuO 2 is readily chlorinated with CCl 4 vapours at a feeding rate of 10 ml/min. In contrast to uranium, chloride forms of plutonium in a highest oxidized state are unstable and are reduced in the melt to Pu(3) and Pu(4). The oxygen being released is retained by CCl 4 and by the products of CCl 4 pyrolysis

Ionic effects on the uptake of chloromercuribenzene-p-sulphonic acid by pancreatic islets

Energy Technology Data Exchange (ETDEWEB)

Soederberg, M; Taeljedal, I B [Umeaa Univ. (Sweden)

1977-01-01

Effects of inorganic ions on the uptake of chloromercuribenzene-p-sulphonic acid (CMBS) were studied in microdissected pancreatic islets on non-inbred ob/ob-mice. Na/sub 2/SO/sub 4/ stimulated the total islet cell uptake of CMBS but decreased the amount of CMBS remaining in islets after brief washing with L-cysteine. CaCl/sub 2/ stimulated both the total and the cysteine-non-displaceable uptake; the stimulatory effect of CaCl/sub 2/ on the cysteine-non-displaceable CMBS uptake was counteracted by Na/sub 2/SO/sub 4/. NaCl, KCl, or choline chloride had no significant effect on the total islet cell uptake of CMBS, whereas LiCl was stimulatory. It is concluded that ..beta..-cells resemble erythrocytes in having a permeation path for CMBS that is inhibited by SO/sub 4//sup 2 -/. By analogy with existing models of the erythrocyte membrane, it is suggested that the SO/sub 4//sup 2 -/-sensitive path leads to sulphydryl groups controlling monovalent cationic permeability in ..beta..-cells.

Determination of hydrolysis constants for gadolinium in ion strength media 2M of NaCl, NaClO4 and KCl at 303 K

International Nuclear Information System (INIS)

Serna M, S.; Jimenez R, M.; Solache R, M.

1999-01-01

This work was made with the purpose to extend information about the hydrolysis constants of gadolinium (III) in ion strength media 2M of NaCl, NaClO 4 , KCl at 303 K using the potentiometric method for this determination, and analysing starting from those data, the influence of anions and cations. It is concluded that the media which were determined the hydrolysis constants are very important and it is recommended the sodium perchlorate as the more adequate salt for those determinations. Also it was obtained the distribution diagrams of chemical species in each one of the media studied. (Author)

Reoxidation of uranium metal immersed in a Li{sub 2}O-LiCl molten salt after electrolytic reduction of uranium oxide

Energy Technology Data Exchange (ETDEWEB)

Choi, Eun-Young, E-mail: eychoi@kaeri.re.kr [Korea Atomic Energy Research Institute, Daedoek-daero 989-111, Yuseong-gu, Daejeon 34057 (Korea, Republic of); Jeon, Min Ku [Korea Atomic Energy Research Institute, Daedoek-daero 989-111, Yuseong-gu, Daejeon 34057 (Korea, Republic of); Department of Quantum Energy Chemical Engineering, University of Science and Technology, Gajeong-ro 217, Yuseong-gu, Daejeon 34113 (Korea, Republic of); Lee, Jeong [Korea Atomic Energy Research Institute, Daedoek-daero 989-111, Yuseong-gu, Daejeon 34057 (Korea, Republic of); Kim, Sung-Wook [Korea Atomic Energy Research Institute, Daedoek-daero 989-111, Yuseong-gu, Daejeon 34057 (Korea, Republic of); Department of Quantum Energy Chemical Engineering, University of Science and Technology, Gajeong-ro 217, Yuseong-gu, Daejeon 34113 (Korea, Republic of); Lee, Sang Kwon [Korea Atomic Energy Research Institute, Daedoek-daero 989-111, Yuseong-gu, Daejeon 34057 (Korea, Republic of); Lee, Sung-Jai [Korea Atomic Energy Research Institute, Daedoek-daero 989-111, Yuseong-gu, Daejeon 34057 (Korea, Republic of); Department of Quantum Energy Chemical Engineering, University of Science and Technology, Gajeong-ro 217, Yuseong-gu, Daejeon 34113 (Korea, Republic of); Heo, Dong Hyun; Kang, Hyun Woo; Jeon, Sang-Chae; Hur, Jin-Mok [Korea Atomic Energy Research Institute, Daedoek-daero 989-111, Yuseong-gu, Daejeon 34057 (Korea, Republic of)

2017-03-15

We present our findings that uranium (U) metal prepared by using the electrolytic reduction process for U oxide (UO{sub 2}) in a Li{sub 2}O–LiCl salt can be reoxidized into UO{sub 2} through the reaction between the U metal and Li{sub 2}O in LiCl. Two salt types were used for immersion of the U metal: one was the salt used for electrolytic reduction, and the other was applied to the unused LiCl salts with various concentrations of Li{sub 2}O and Li metal. Our results revealed that the degree of reoxidation increases with the increasing Li{sub 2}O concentration in LiCl and that the presence of the Li metal in LiCl suppresses the reoxidation of the U metal. - Highlights: • Uranium (U) metal can be reoxidized into UO{sub 2} through the reaction between the U metal and Li{sub 2}O in LiCl. • The degree of reoxidation increases with the Li{sub 2}O concentration in LiCl. • The presence of the Li metal in LiCl suppresses the reoxidation of the U metal.

Fundamental study on the salt distillation from the mixtures of rare earth precipitates and LiCl-KCl eutectic salt

International Nuclear Information System (INIS)

Yang, H. C.; Eun, H. C.; Cho, Y. Z.; Lee, H. S.; Kim, I. T.

2008-01-01

An electrorefining process of spent nuclear fuel generates waste salt containing some radioactive metal chlorides. The most effective method to reduce salt waste volume is to separate radioactive metals from non-radioactive salts. A promising approach is to change radioactive metal chlorides into salt-insoluble oxides by an oxygen sparging. Following this, salt distillation process is available to effectively separate the precipitated particulate metal oxides from salt. This study investigated the distillation rates of LiCl-KCl eutectic salt under different vacuums at elevated temperatures. The first part study investigated distillation rates of eutectic salt under different vacuums at high temperatures by using thermo-gravimetric furnace system. In the second part, we tested the removal of eutectic salt from the RE precipitates by using the laboratory vacuum distillation furnace system. Investigated variables were the temperature of mixture, the degree of vacuum and the time

Electrochemical deposition of La-Mg alloys in LaCl3-MgCl2-KCl system with molten salt electrolysis process

Directory of Open Access Journals (Sweden)

Sahoo Kumar D.

2014-01-01

Full Text Available La-Mg alloys of different compositions were prepared by electrolysis of LaCl3-MgCl2-KCl melts. Different phases of La-Mg alloys were characterized by X-ray diffraction (XRD and Scanning Electron Microscopy (SEM. Energy dispersive spectrometry (EDS and Inductively Coupled Plasma-Atomic Emission Spectroscopy (ICP-AES analyses showed that chemical compositions of La-Mg alloys were consistent with phase structures of XRD pattern, and magnesium content in the alloy could be controlled by electrolysis parameters. The effects of various process parameters such as concentration of magnesium chloride in the bath, temperature of electrolysis and cathode current density on the current efficiency have been investigated. A maximum current efficiency of 85% and yield of 80% was obtained from the bath at 12.5A/cm2 current density at an operating temp 850°C.

Lithium chloride inhibits early stages of foot-and-mouth disease virus (FMDV) replication in vitro.

Science.gov (United States)

Zhao, Fu-Rong; Xie, Yin-Li; Liu, Ze-Zhong; Shao, Jun-Jun; Li, Shi-Fang; Zhang, Yong-Guang; Chang, Hui-Yun

2017-11-01

Foot-and-mouth disease virus (FMDV) causes an economically important and highly contagious disease of cloven-hoofed animals such as cattle, swine, and sheep. FMD vaccine is the traditional way to protect against the disease, which can greatly reduce its occurrence. However, the use of FMD vaccines to protect early infection is limited. Therefore, the alternative strategy of applying antiviral agents is required to control the spread of FMDV in outbreak situations. As previously reported, LiCl has obviously inhibition effects on a variety of viruses such as transmissible gastroenteritis virus (TGEV), infectious bronchitis coronavirus (IBV), and pseudorabies herpesvirus and EV-A71 virus. In this study, our findings were the first to demonstrate that LiCl inhibition of the FMDV replication. In this study, BHK-21 cell was dose-dependent with LiCl at various stages of FMDV. Virus titration assay was calculated by the 50% tissue culture infected dose (TCID 50 ) with the Reed and Muench method. The cytotoxicity assay of LiCl was performed by the CCK8 kit. The expression level of viral mRNA was measured by RT-qPCR. The results revealed LiCl can inhibit FMDV replication, but it cannot affect FMDV attachment stage and entry stage in the course of FMDV life cycle. Further studies confirmed that the LiCl affect the replication stage of FMDV, especially the early stages of FMDV replication. So LiCl has potential as an effective anti-FMDV drug. Therefore, LiCl may be an effective drug for the control of FMDV. Based on that, the mechanism of the antiviral effect of LiCl on FMDV infection is need to in-depth research in vivo. © 2017 Wiley Periodicals, Inc.

Lithium chloride attenuates mitomycin C induced necrotic cell death in MDA-MB-231 breast cancer cells via HMGB1 and Bax signaling.

Science.gov (United States)

Razmi, Mahdieh; Rabbani-Chadegani, Azra; Hashemi-Niasari, Fatemeh; Ghadam, Parinaz

2018-07-01

The clinical use of potent anticancer drug mitomycin C (MMC) has limited due to side effects and resistance of cancer cells. The aim of this study was to investigate whether lithium chloride (LiCl), as a mood stabilizer, can affect the sensitivity of MDA-MB-231 breast cancer cells to mitomycin C. The cells were exposed to various concentrations of mitomycin C alone and combined with LiCl and the viability determined by trypan blue and MTT assays. Proteins were analyzed by western blot and mRNA expression of HMGB1 MMP9 and Bcl-2 were analyzed by RT-PCR. Flow cytometry was used to determine the cell cycle arrest and percent of apoptotic and necrotic cells. Concentration of Bax assessed by ELISA. Exposure of the cells to mitomycin C revealed IC 50 value of 20 μM, whereas pretreatment of the cells with LiCl induced synergistic cytotoxicity and IC 50 value declined to 5 μM. LiCl combined with mitomycin C significantly down-regulated HMGB1, MMP9 and Bcl-2 gene expression but significantly increased the level of Bax protein. In addition, the content of HMGB1 in the nuclei decreased and pretreatment with LiCl reduced the content of HMGB1 release induced by MMC. LiCl increased mitomycin C-induced cell shrinkage and PARP fragmentation suggesting induction of apoptosis in these cells. LiCl prevented mitomycin C-induced necrosis and changed the cell death arrest at G2/M-phase. Taking all together, it is suggested that LiCl efficiently enhances mitomycin C-induced apoptosis and HMGB1, Bax and Bcl-2 expression may play a major role in this process, the findings that provide a new therapeutic strategy for LiCl in combination with mitomycin C. Copyright © 2018 Elsevier GmbH. All rights reserved.

Effects of lithium chloride as a potential radioprotective agent on radiation response of DNA synthesis in mouse germinal cells.

Science.gov (United States)

Bhattacharjee, D; Rajan, R; Krishnamoorthy, L; Singh, B B

1997-06-01

Mouse spermatogonial germ cells are highly sensitive to ionizing radiation. Lithium salts are reported to stimulate the postirradiation recovery of hematopoietic marrow cells. We have, therefore, examined whether administered lithium chloride (LiCl) would also be able to protect the mouse germinal cells against radiation injury. Taking DNA synthesis as an endpoint, our results show that the testicular DNA-specific activity in irradiated mice was higher by 61% on average when they had been pretreated with LiCl both 24 h and 1 h prior to gamma-irradiation (2.0 Gy). It was also observed that the DNA synthetic activity in the germinal cells fully recovered after LiCl pretreatment at doses of 40 mg per kg body weight prior to total body irradiation of 0.05-0.25 Gy, whereas at doses of 0.5-6.0 Gy, following the same procedure of LiCl pretreatment, only an incomplete recovery was observed. The dose reduction factor for LiCl is 1.84. The current findings indicate that pretreatment with LiCl provides considerable protection against radiation damage in mouse spermatogonia.

Influence of reaction products of K-getter fuel additives on commercial vanadia-based SCR catalysts Part II. Simultaneous addition of KCl, Ca(OH)(2), H3PO4 and H2SO4 in a hot flue gas at a SCR pilot-scale setup

DEFF Research Database (Denmark)

Castellino, Francesco; Jensen, Anker Degn; Johnsson, Jan Erik

2009-01-01

A commercial V2O5-WO3-TiO2 corrugated-type SCR monolith has been exposed for 1000 h in a pilot-scale setup to a flue gas doped with KCl, Ca(OH)(2), H3PO4 and H2SO4 by spraying a water solution of the components into the hot flue gas. The mixture composition has been adjusted in order to have P...... surface and did not proceed at the fast rates known for KCl. This fact indicates that binding K in P-K-Ca compounds is an effective way to reduce the negative influence of alkali metals on the lifetime of the vanadia-based SCR catalysts. On the other hand, P-deposition was favoured by the formation...

Recovery of uranium from uranium and lanthanides in LiCl-KCl molten salt by electrowinning including Cd-Li anode

International Nuclear Information System (INIS)

Woo, Moon Shik; Kim, Eung Ho

2005-01-01

A trans-uranium (TRU) fuel should be manufactured and loaded in transmutation systems in order to transmute the long-lived TRU nuclides into short-lived ones. However, since all of the TRU nuclides are not completely transmuted in one cycle lifetime in transmutation systems, the spent TRU fuel has to be treated to recover the long-lived radionuclides or fuel matrix materials. One concept to manufacture TRU fuel for transmutation is to recover uranium from TRU and molten salt. If this type of fuel is adopted for transmutation, uranium could also be an objective material to be recovered and recycled. Since electrowinning is a promising technology to be employed for the recovery of uranium from fuel materials, some experimental work of electrowinning using anode of Cd-Li alloy was carried out in this study. The basic salt chosen was a mixture of LiCl-KCl which has an eutectic point at 357 .deg. C

Following the electroreduction of uranium dioxide to uranium in LiCl–KCl eutectic in situ using synchrotron radiation

Energy Technology Data Exchange (ETDEWEB)

Brown, L.D.; Abdulaziz, R.; Jervis, R.; Bharath, V.J. [Electrochemical Innovation Lab, Dept. Chemical Engineering, UCL, London WC1E 7JE (United Kingdom); Atwood, R.C.; Reinhard, C.; Connor, L.D. [Diamond Light Source, Harwell Science and Innovation Campus, Didcot, Oxfordshire OX11 0DE (United Kingdom); Simons, S.J.R.; Inman, D.; Brett, D.J.L. [Electrochemical Innovation Lab, Dept. Chemical Engineering, UCL, London WC1E 7JE (United Kingdom); Shearing, P.R., E-mail: p.shearing@ucl.ac.uk [Electrochemical Innovation Lab, Dept. Chemical Engineering, UCL, London WC1E 7JE (United Kingdom)

2015-09-15

Highlights: • We investigated the electroreduction of UO{sub 2} to U in LiCl/KCL eutectic molten salt. • Combined electrochemical measurement and in situ XRD is utilised. • The electroreduction appears to occur in a single, 4-electron-step, process. • No intermediate compounds were observed. - Abstract: The electrochemical reduction of uranium dioxide to metallic uranium has been investigated in lithium chloride–potassium chloride eutectic molten salt. Laboratory based electrochemical studies have been coupled with in situ energy dispersive X-ray diffraction, for the first time, to deduce the reduction pathway. No intermediate phases were identified using the X-ray diffraction before, during or after electroreduction to form α-uranium. This suggests that the electrochemical reduction occurs via a single, 4-electron-step, process. The rate of formation of α-uranium is seen to decrease during electrolysis and could be a result of a build-up of oxygen anions in the molten salt. Slow transport of O{sup 2−} ions away from the UO{sub 2} working electrode could impede the electrochemical reduction.

Effects of lithium chloride as a potential radioprotective agent on radiation response of DNA synthesis in mouse germinal cells

Energy Technology Data Exchange (ETDEWEB)

Bhattacharjee, D. [Radiation Biology and Biochemistry Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Rajan, R. [Radiation Biology and Biochemistry Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Krishnamoorthy, L. [Kidwai Memorial Institute of Oncology, Bangalore 560 029 (India); Singh, B.B. [Radiation Biology and Biochemistry Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India)

1997-06-01

Mouse spermatogonial germ cells are highly sensitive to ionizing radiation. Lithium salts are reported to stimulate the postirradiation recovery of hematopoietic marrow cells. We have, therefore, examined whether administered lithium chloride (LiCl) would also be able to protect the mouse germinal cells against radiation injury. Taking DNA synthesis as an endpoint, our results show that the testicular DNA-specific activity in irradiated mice was higher by 61% on average when they had been pretreated with LiCl both 24 h and 1 h prior to {gamma}-irradiation (2.0 Gy). It was also observed that the DNA synthetic activity in the germinal cells fully recovered after LiCl pretreatment at doses of 40 mg per kg body weight prior to total body irradiation of 0.05-0.25 Gy, whereas at doses of 0.5-6.0 Gy, following the same procedure of LiCl pretreatment, only an incomplete recovery was observed. The dose reduction factor for LiCl is 1.84. The current findings indicate that pretreatment with LiCl provides considerable protection against radiation damage in mouse spermatogonia. (orig.). With 3 tabs.

NONOates regulate KCl cotransporter-1 and -3 mRNA expression in vascular smooth muscle cells.

Science.gov (United States)

Di Fulvio, Mauricio; Lauf, Peter K; Shah, Shalin; Adragna, Norma C

2003-05-01

Nitric oxide (NO) donors regulate KCl cotransport (KCC) activity and cotransporter-1 and -3 (KCC1 and KCC3) mRNA expression in sheep erythrocytes and in primary cultures of rat vascular smooth muscle cells (VSMCs), respectively. In this study, we used NONOates as rapid and slow NO releasers to provide direct evidence implicating NO as a regulator of KCC3 gene expression at the mRNA level. In addition, we used the expression of KCC3 mRNA to further investigate the mechanism of action of these NO donors at the cellular level. Treatment of VSMCs with rapid NO releasers, like NOC-5 and NOC-9, as well as with the direct NO-independent soluble guanylyl cyclase (sGC) stimulator YC-1, acutely increased KCC3 mRNA expression in a concentration- and time-dependent manner. The slow NO releaser NOC-18 had no effect on KCC3 gene expression. A specific NO scavenger completely prevented the NONOate-induced KCC3 mRNA expression. Inhibition of sGC with LY-83583 blocked the NONOate- and YC-1-induced KCC3 mRNA expression. This study shows that in primary cultures of rat VSMCs, the fast NO releasers NOC-9 and NOC-5, but not the slow NO releaser NOC-18, acutely upregulate KCC3 mRNA expression in a NO/sGC-dependent manner.

Fundamental Study on a Distillation Separation of a LiCl-KCl Eutectic Salt from Rare Earth Precipitates

International Nuclear Information System (INIS)

Yang, Hee Chul; Eun, Hee Chul; Kim, In Tae

2010-01-01

The distillation rate on LiCl-KCl eutectic salt under different vacuums from 0.5-50 mmHg was first investigated by using both a non-isothermal and a isothermal thermogravimetric (TG) analysis. Based on the non-isothermal TG data, distillation rate equations as a function of the temperature could be derived. Calculated flux by these model flux equations was in agreement with the distillation rate obtained from isothermal TG analysis. A distillation rate of 10 -4 -10 -5 mole cm -2 sec -1 is obtainable at temperatures less than 1300 K and vacuums of 0.5-50 mmHg. About a 99% salt distillation efficiency was obtained after an hour at a temperature above 1150 K under 50 mmHg in a small scale distillation test system. An increase in the vaporizing surface area is relatively effective for removing residual salt in the remaining particles, when compared to that for the vaporizing time. Over 99.95% of total distillation efficiency was obtained for a 1-h distillation operation by increasing the inner surface area from 4.52 cm 2 to 12.56 cm 2 .

The off-center effect on the diffusion coefficient of Cu+ and Li+ in the KCl lattice

International Nuclear Information System (INIS)

Despa, F.

1994-07-01

It is well known that the diffusion coefficients of the Cu + cation in the NaCl and KCl lattices exceeds by three or four orders of magnitude the corresponding self-diffusion coefficients in the intrinsic temperature regions. This fast diffusion of the Cu + has been explained in many papers as an interstitial diffusion although the optical spectra do not confirm the existence of interstitial Cu + . In this paper we propose a new mechanism for fast diffusion. The model assumes that the equilibrium positions of the cationic impurities are noncentral and that the diffusion proceeds by hopping across the potential barrier along the nonlinear paths with the highest probability. The main result shows that the off-center position enhances considerably the diffusion. Theoretical diffusion coefficients have been obtained by modelling the potential barrier. Changes of the configuration entropy and the vibration spectra due to the presence of the noncentral impurity have been included in the model. We proceeded in the Li + cation case as in the case of Cu + cation. We emphasize the good agreement of the model with the experimental data and we show that if the impurity is placed close to the central site the due diffusion coefficient is close to that for the cationic self-diffusion. (author). 37 refs, 6 figs, 3 tabs

Lithium fluxes indicate presence of Na-Cl cotransport (NCC) in human lens epithelial cells.

Science.gov (United States)

Lauf, Peter K; Chimote, Ameet A; Adragna, Norma C

2008-01-01

During regulatory volume decrease (RVD) of human lens epithelial cells (hLECs) by clotrimazole (CTZ)-sensitive K fluxes, Na-K-2Cl cotransport (NKCC) remains active and K-Cl cotransport (KCC) inactive. To determine whether such an abnormal behavior was caused by RVD-induced cell shrinkage, NKCC was measured in the presence of either CTZ or in high K media to prevent RVD. NKCC transports RbCl + NaCl, and LiCl + KCl; thus ouabain-insensitive, bumetanide-sensitive (BS) or Cl-dependent (ClD) Rb and Li fluxes were determined in hyposmotic high NaCl media with CTZ, or in high KCl media alone, or with sulfamate (Sf) or nitrate as Cl replacement at varying Rb, Li or Cl mol fractions (MF). Unexpectedly, NKCC was inhibited by 80% with CTZ (IC(50) = 31 microM). In isosmotic (300 mOsM) K, Li influx was approximately 1/3 of Rb influx in Na, 50% lower in Sf, and bumetanide-insensitive (BI). In hypotonic (200 mOsM) K, only the ClD but not BS Li fluxes were detected. At Li MFs from 0.1-1, Li fluxes fitted a bell-shaped curve maxing at approximately 0.6 Li MF, with the BS fluxes equaling approximately 1/4 of the ClD-Li influx. The difference, i.e. the BI/ClD Li influx, saturated with increasing Li and Cl MFs, with K(ms) for Li of 11 with, and 7 mM without K, and of approximately 46 mM for Cl. Inhibition of this K-independent Li influx by thiazides was weak whilst furosemide (<100 microM) was ineffective. Reverse transcription polymerase chain reaction and Western blots verified presence of both NKCC1 and Na-Cl cotransport (NCC). In conclusion, in hyposmotic high K media, which prevents CTZ-sensitive K flux-mediated RVD in hLECs, NKCC1, though molecularly expressed, was functionally silent. However, a K-independent and moderately thiazide-sensitive ClD-Li flux, i.e. LiCC, likely occurring through NCC was detected operationally and molecularly. (c) 2008 S. Karger AG, Basel.

Isopiestic determination of the osmotic and activity coefficients of the {l_brace}yKCl + (1 - y)K{sub 2}HPO{sub 4}{r_brace}(aq) system at T = 298.15 K

Energy Technology Data Exchange (ETDEWEB)

Popovic, Daniela Z. [Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, 11 001 Belgrade (Serbia); Miladinovic, Jelena, E-mail: duma@tmf.bg.ac.rs [Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, 11 001 Belgrade (Serbia); Todorovic, Milica D.; Zrilic, Milorad M. [Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, 11 001 Belgrade (Serbia); Rard, Joseph A., E-mail: solution_chemistry2@comcast.net [4363 Claremont Way, Livermore, CA 94550 (United States)

2011-12-15

Highlights: > Isopiestic measurements were made for {l_brace}yKCl + (1 - y)K{sub 2}HPO{sub 4}{r_brace}(aq) at T = 298.15 K. > The resulting osmotic coefficients were represented by three thermodynamic models. > Activity coefficients from Pitzer model with Scatchard mixing terms are recommended. - Abstract: The osmotic coefficients of aqueous mixtures of KCl and K{sub 2}HPO{sub 4} have been measured at T = (298.15 {+-} 0.01) K by the isopiestic vapor pressure method over the range of ionic strengths from (2.3700 to 11.250) mol . kg{sup -1} using CaCl{sub 2}(aq) as the reference solution. Our new experimental results were modeled with an extended form of Pitzer's ion-interaction model equations, both with the usual mixing terms and with Scatchard's neutral-electrolyte mixing terms, and with the Clegg-Pitzer-Brimblecombe equations based on the mole-fraction-composition scale. There is a dearth of previously published isopiestic data for mixtures containing salts of HPO{sub 4}{sup 2-}(aq) and, consequently, no previous measurements are available for comparison with the present results. The present study yields Cl{sup -}HPO{sub 4}{sup 2-} mixing parameters for these three models that are needed for modeling the thermodynamic activities of solute components of natural waters and other complex aqueous electrolyte mixtures.

Molecular dynamics study of structure and vibrational spectra at zwitterionoic lipid/aqueous KCl, NaCl, and CaCl2 solution interfaces

Science.gov (United States)

Ishiyama, Tatsuya; Shirai, Shinnosuke; Okumura, Tomoaki; Morita, Akihiro

2018-06-01

Molecular dynamics (MD) simulations of KCl, NaCl, and CaCl2 solution/dipalmytoylphosphatidylcholine lipid interfaces were performed to analyze heterodyne-detected vibrational sum frequency generation (HD-VSFG) spectra in relation to the interfacial water structure. The present MD simulation well reproduces the experimental spectra and elucidates a specific cation effect on the interfacial structure. The K+, Na+, and Ca2+ cation species penetrate in the lipid layer more than the anions in this order, due to the electrostatic interaction with negative polar groups of lipid, and the electric double layer between the cations and anions cancels the intrinsic orientation of water at the water/lipid interface. These mechanisms explain the HD-VSFG spectrum of the water/lipid interface and its spectral perturbation by adding the ions. The lipid monolayer reverses the order of surface preference of the cations at the solution/lipid interface from that at the solution/air interface.

Influence of ionic strength in the adsorption and during photocatalysis of reactive black 5 azo dye on TiO2 coated on non woven paper with SiO2 as a binder

International Nuclear Information System (INIS)

Aguedach, Abdelkahhar; Brosillon, Stephan; Morvan, Jean; Lhadi, El Kbir

2008-01-01

Reactive black 5 (RB5), an azo dye, was degraded by using UV-irradiated TiO 2 coated on non woven paper with SiO 2 as a binder. The adsorption capacity of the photocatalyst was studied at natural pH, superior to pH pzc of the binder, for various ionic strengths. Different salts such as NaCl, KCl, CaCl 2 , LiCl, Ca(NO 3 ) 2 were used to increase the ionic strength. The presence of salt increased the adsorption capacity. The electrostatic interactions between dye and oxide surface charges (TiO 2 /SiO 2 ) is very important in the adsorption phenomena. The effect of the ionic strength of the solution on photocatalyst degradation was studied. The rate of degradation was increased by the presence of salts in the range of the experimental conditions. The increase of the initial decolorization rate was observed in the following order: Ca 2+ > K + > Na + > Li + . Experiments with different anions (Cl - , NO 3 - ) had shown that nitrate was an indifferent electrolyte for the adsorption and photodegradation of the dye on SiO 2 /TiO 2

Actinide, lanthanide and fission product speciation and electrochemistry in high and low temperature ionic melts

Energy Technology Data Exchange (ETDEWEB)

Bhatt, Anand I.; Kinoshita, Hajime; Koster, Anne L.; May, Iain; Sharrad, Clint A.; Volkovich, Vladimir A.; Fox, O. Danny; Jones, Chris J.; Lewin, Bob G.; Charnock, John M.; Hennig, Christoph

2004-07-01

There is currently a great deal of research interest in the development of molten salt technology, both classical high temperature melts and low temperature ionic liquids, for the electrochemical separation of the actinides from spent nuclear fuel. We are interested in gaining a better understanding of actinide and key fission product speciation and electrochemical properties in a range of melts. Our studies in high temperature alkali metal melts (including LiCl and LiCl-KCl and CsCl-NaCl eutectics) have focussed on in-situ species of U, Th, Tc and Ru using X-ray absorption spectroscopy (XAS, both EXAFS and XANES) and electronic absorption spectroscopy (EAS). We report unusual actinide speciation in high temperature melts and an evaluation of the likelihood of Ru or Tc volatilization during plant operation. Our studies in lower temperature melts (ionic liquids) have focussed on salts containing tertiary alkyl group 15 cations and the bis(tri-fluor-methyl)sulfonyl)imide anion, melts which we have shown to have exceptionally wide electrochemical windows. We report Ln, Th, U and Np speciation (XAS, EAS and vibrational spectroscopy) and electrochemistry in these melts and relate the solution studies to crystallographic characterised benchmark species. (authors)

Actinide, lanthanide and fission product speciation and electrochemistry in high and low temperature ionic melts

International Nuclear Information System (INIS)

Bhatt, Anand I.; Kinoshita, Hajime; Koster, Anne L.; May, Iain; Sharrad, Clint A.; Volkovich, Vladimir A.; Fox, O. Danny; Jones, Chris J.; Lewin, Bob G.; Charnock, John M.; Hennig, Christoph

2004-01-01

There is currently a great deal of research interest in the development of molten salt technology, both classical high temperature melts and low temperature ionic liquids, for the electrochemical separation of the actinides from spent nuclear fuel. We are interested in gaining a better understanding of actinide and key fission product speciation and electrochemical properties in a range of melts. Our studies in high temperature alkali metal melts (including LiCl and LiCl-KCl and CsCl-NaCl eutectics) have focussed on in-situ species of U, Th, Tc and Ru using X-ray absorption spectroscopy (XAS, both EXAFS and XANES) and electronic absorption spectroscopy (EAS). We report unusual actinide speciation in high temperature melts and an evaluation of the likelihood of Ru or Tc volatilization during plant operation. Our studies in lower temperature melts (ionic liquids) have focussed on salts containing tertiary alkyl group 15 cations and the bis(tri-fluor-methyl)sulfonyl)imide anion, melts which we have shown to have exceptionally wide electrochemical windows. We report Ln, Th, U and Np speciation (XAS, EAS and vibrational spectroscopy) and electrochemistry in these melts and relate the solution studies to crystallographic characterised benchmark species. (authors)

Current view on the functional regulation of the neuronal K+-Cl- cotransporter KCC2

Directory of Open Access Journals (Sweden)

Igor eMedina

2014-02-01

Full Text Available In the mammalian central nervous system, the inhibitory strength of chloride (Cl--permeable GABAA and glycine receptors (GABAAR and GlyR depends on the intracellular Cl- concentration ([Cl-]i. Lowering [Cl-]i enhances inhibition, whereas raising [Cl-]i facilitates neuronal activity. A neuron’s basal level of [Cl-]i, as well as its Cl- extrusion capacity, is critically dependent on the activity of the electroneutral K+-Cl- cotransporter KCC2, a member of the SLC12 cation-Cl- cotransporter (CCC family. KCC2 deficiency compromises neuronal migration, formation and the maturation of GABAergic and glutamatergic synaptic connections, and results in network hyperexcitability and seizure activity. Several neurological disorders including multiple epilepsy subtypes, neuropathic pain, and schizophrenia, as well as various insults such as trauma and ischemia, are associated with significant decreases in the Cl- extrusion capacity of KCC2 that result in increases of [Cl-]i and the subsequent hyperexcitability of neuronal networks. Accordingly, identifying the key upstream molecular mediators governing the functional regulation of KCC2, and modifying these signalling pathways with small molecules, might constitute a novel neurotherapeutic strategy for multiple diseases. Here, we discuss recent advances in the understanding of the mechanisms regulating KCC2 activity, and of the role these mechanisms play in neuronal Cl- homeostasis and GABAergic neurotransmission. As KCC2 mediates electroneutral transport, the experimental recording of its activity constitutes an important research challenge; we therefore also, provide an overview of the different methodological approaches utilized to monitor function of KCC2 in both physiological and pathological conditions.

Vibrational spectroscopy of hydrated potassium hexauranate for the phase study of the UO3-KCl-H2O system

International Nuclear Information System (INIS)

Dothee, Daniel.

1980-02-01

In the study of the UO 3 -KCl-H 2 O system, a phase, called C phase, was isolated; it has a radiocrystallogram very close to the hexauranate K 2 U 6 O 19 ,11H 2 O, but K + and Cl - are found in its composition. Links between these two phases are studied and especially structure relationships. Hydrated potassium hexauranate structure was determined previously with a natural crystal. Position of potassium and uranium atoms only are known. As monocrystal preparation is impossible a direct structural study is impossible too. Vibrational spectroscopic analysis was selected for this study. Hexauranate structure is determined and results are extended for the study of the C phase. The hydrate UO 3 .0.8 H 2 O a stable and well defined compound is chosen for the hydrothermal synthesis of the different phases. Four main phases are evidenced: the chloro-uranate Ksub(x)UO 3 Clsub(x) (already known), a hydrated potassium uranate and two phases (one is the C phase) containing chloride ions are intermediaries between the chloro-uranate and the uranate [fr

Thermodynamics properties of plutonium in NaCl-KCl and CaCl2 at 1073 K and in liquid gallium

International Nuclear Information System (INIS)

Lambertin, D.; Ched'homme, S.; Bourges, G.; Pescayre, L.; Sanchez, S.; Picard, G.

2004-01-01

Cadmium and bismuth metal are mostly used as solvent in nuclear pyrochemical processes and especially in actinides/lanthanides separations. Gallium metal has been chosen because no literature values are available with plutonium and its regeneration by refining at low temperature is possible. Electrochemical window of gallium metal and activity coefficient of plutonium in gallium have been determined by using potentiometric method. Secondly, the electrochemical properties of plutonium have been studied in molten equimolar NaCl/KCl and CaCl 2 at 1073 K by cyclic voltammetry. The standard potentials of Pu(III)/Pu redox couple, respectively, -2,54 V and -2,51 V, led to the calculation of the activity coefficients of Pu(III). In CaCl 2 the complexation of Pu(III) ions is lower and the voltage gap between Pu(III)/Pu couple and the solvent limit is higher. The new data on plutonium electrochemistry in molten chlorides and liquid gallium media combined with literature data on lanthanides suggest that gallium can be a good solvent metal for pyro-chemistry separation. (authors)

Electron spin ressonance of radicals produced by ultra-violet photolysis of KCL dopped with potassium cyanide and potassium cyanate

International Nuclear Information System (INIS)

Duran, J.E.R.

1975-01-01

The production of radicals by ultra-violet photolysis of KCL dopped with potassium cyanide and potassium cyanate is studied by electron spin resonance. Several new paramagnetic species are detected which are identified as HCNO - , NCN - /NCNO - , CNN - /CNON - and CNOsup(=) all giving isotropic spectra at 77 0 K. The temperature dependence of the CNOsup(=) spectrum is investigated down to 1.6 0 K. It is found that two different recrientation motions ocurr which freeze at different temperatures. The effect of this motion on the line width is analized using Anderson's theory of exchange narrowing. The electronic structure of the CNOsup(=) radical is discussed using the measured the carbon and nitrogen hfs constants. It is found that a bonding scheme similar to that accepted for the isoelectronic molecule NO 2 is applicable, and a one electron molecular orbital scheme is given. Within this scheme a negative contribution to the nitrogen isotropic hfs constant is found which is assumed to originate from the polarization of the fully occupied ls orbitals [pt

Strong quadrupole interaction in electron paramagnetic resonance. Study of the indium hexacyanide (III) in KCl irradiated with electrons

International Nuclear Information System (INIS)

Vugman, N.V.

1973-08-01

The radiation effects in ]Ir III (CN) 6 ] 3- diamagnetic complexe inserted in the KCl lattice and irradiated with electrons of 2MeV by electron spin resonance (ESR) are analysed. Formulas for g and A tensors in the ligand field approximation, are derivated to calculate non coupling electron density in the metal. The X polarization field of inner shells is positive, indicating a 6s function mixture in the non coupling electron molecular orbital. The observed hyperfine structure is assigned to 4 equivalent nitrogen and one non equivalent nitrogen. This hypothesis is verified by experience of isotope substitution with 15 N. The s and p spin density in ligands are calculated and discussed in terms of molecular obitals. The effects of strong quadrupole interaction into the EPR spectra of ]Ir II (CN) 5 ] 3- complex are analysed by MAGNSPEC computer program to diagonalize the Spin Hamiltonian of the system. Empiric rules for EPR espectrum interpretation with strong quadrupole interaction. A review of EPR technique and a review of main concepts of crystal-field and ligand field theories, are also presented. (M.C.K.) [pt

Correlation between the extracting solutions, Modified KCl-Olsen and Mehlich 3, used in soil laboratories in Costa Rica

International Nuclear Information System (INIS)

Bertsch, Floria; Bejarano, Jose Antonio; Corrales, Marco

2005-01-01

The correlation found, between the 2 most commonly used extraction solutions in soil laboratories of Costa Rica, is discussed for Ca, Mg, K, Zn and P determinations in soil analyses. Given the coexistence of extraction methodologies, it is of great relevance to provide users with information allowing an adequate interpretation of the analysis results. Using data exchanged among laboratories, at the national level, relationships between modified KCl-Olsen and Mehlich 3 solutions were established. For all elements determined, except for P, the association between both solutions is very clear and well-defined. Both solutions extract the same amounts of Ca and Mg; Mehlich 3 extracts 1.5 times more K than Modified Olsen. In the case of Zn, in Ca-rich soils (>10 cmol(+) 1 -1 ) Mehlich 3 extracts more Zn, so the critical level must be raised to 3.5 mg 1''- 1 ; whereas, in soils low in Ca ( -1 ), Mehlich 3 extracts less Zn than Modified Olsen, so the critical level must be lowered to 2.5 mg 1 -1 . As for P, the association is not clear at all. (author) [es

Transcription arrest by a G quadruplex forming-trinucleotide repeat sequence from the human c-myb gene.

Science.gov (United States)

Broxson, Christopher; Beckett, Joshua; Tornaletti, Silvia

2011-05-17

Non canonical DNA structures correspond to genomic regions particularly susceptible to genetic instability. The transcription process facilitates formation of these structures and plays a major role in generating the instability associated with these genomic sites. However, little is known about how non canonical structures are processed when encountered by an elongating RNA polymerase. Here we have studied the behavior of T7 RNA polymerase (T7RNAP) when encountering a G quadruplex forming-(GGA)(4) repeat located in the human c-myb proto-oncogene. To make direct correlations between formation of the structure and effects on transcription, we have taken advantage of the ability of the T7 polymerase to transcribe single-stranded substrates and of G4 DNA to form in single-stranded G-rich sequences in the presence of potassium ions. Under physiological KCl concentrations, we found that T7 RNAP transcription was arrested at two sites that mapped to the c-myb (GGA)(4) repeat sequence. The extent of arrest did not change with time, indicating that the c-myb repeat represented an absolute block and not a transient pause to T7 RNAP. Consistent with G4 DNA formation, arrest was not observed in the absence of KCl or in the presence of LiCl. Furthermore, mutations in the c-myb (GGA)(4) repeat, expected to prevent transition to G4, also eliminated the transcription block. We show T7 RNAP arrest at the c-myb repeat in double-stranded DNA under conditions mimicking the cellular concentration of biomolecules and potassium ions, suggesting that the G4 structure formed in the c-myb repeat may represent a transcription roadblock in vivo. Our results support a mechanism of transcription-coupled DNA repair initiated by arrest of transcription at G4 structures.

Reoxidation of uranium metal immersed in a Li2O-LiCl molten salt after electrolytic reduction of uranium oxide

Science.gov (United States)

Choi, Eun-Young; Jeon, Min Ku; Lee, Jeong; Kim, Sung-Wook; Lee, Sang Kwon; Lee, Sung-Jai; Heo, Dong Hyun; Kang, Hyun Woo; Jeon, Sang-Chae; Hur, Jin-Mok

2017-03-01

We present our findings that uranium (U) metal prepared by using the electrolytic reduction process for U oxide (UO2) in a Li2O-LiCl salt can be reoxidized into UO2 through the reaction between the U metal and Li2O in LiCl. Two salt types were used for immersion of the U metal: one was the salt used for electrolytic reduction, and the other was applied to the unused LiCl salts with various concentrations of Li2O and Li metal. Our results revealed that the degree of reoxidation increases with the increasing Li2O concentration in LiCl and that the presence of the Li metal in LiCl suppresses the reoxidation of the U metal.

Thermodynamics of La and U and the separation factor of U/La in fused Me(Ga-40 wt.% In)/3LiCl-2KCl system

Science.gov (United States)

Smolenski, Valeri; Novoselova, Alena; Volkovich, Vladimir A.

2017-11-01

Separation of lanthanides and actinides can be achieved in a unique "molten chloride - liquid metal" system. Electrode potentials were recorded vs. Cl-/Cl2 reference electrode and the temperature dependencies of the apparent standard potentials of La-(Ga-In) and U-(Ga-In) alloys were determined. Thermodynamic properties and separation factor of lanthanum and uranium were calculated. The obtained data show the perspective for using this system in future innovation method for recovery of nuclear waste.

Lithium chloride contributes to blood-spinal cord barrier integrity and functional recovery from spinal cord injury by stimulating autophagic flux.

Science.gov (United States)

Tong, Minji; He, Zili; Lin, Xiaoxiao; Zhou, Yulong; Wang, Qingqing; Zheng, Zengming; Chen, Jian; Xu, Huazi; Tian, Naifeng

2018-01-22

Blood-spinal cord barrier (BSCB) disruption following spinal cord injury (SCI) significantly compromises functional neuronal recovery. Autophagy is a potential therapeutic target when seeking to protect the BSCB. We explored the effects of lithium chloride (LiCl) on BSCB permeability and autophagy-induced SCI both in a rat model of SCI and in endothelial cells subjected to oxygen-glucose deprivation. We evaluated BSCB status using the Evans Blue dye extravasation test and measurement of tight junction (TJ) protein levels; we also assessed functional locomotor recovery. We detected autophagy-associated proteins in vivo and in vitro using both Western blotting and immunofluorescence staining. We found that, in a rat model of SCI, LiCl attenuated the elevation in BSCB permeability, improved locomotor recovery, and inhibited the degradation of TJ proteins including occludin and claudin-5. LiCl significantly induced the extent of autophagic flux after SCI by increasing LC3-II and ATG-5 levels, and abolishing p62 accumulation. In addition, a combination of LiCl and the autophagy inhibitor chloroquine not only partially eliminated the BSCB-protective effect of LiCl, but also exacerbated TJ protein degradation both in vivo and in vitro. Together, these findings suggest that LiCl treatment alleviates BSCB disruption and promotes locomotor recovery after SCI, partly by stimulating autophagic flux. Copyright © 2017 Elsevier Inc. All rights reserved.

Electrochemical behavior of zirconium in the LiCl-KCl molten salt at Mo electrode

Energy Technology Data Exchange (ETDEWEB)

Chen Zeng; Li Yongjun [Key Laboratory of Photovoltaic Materials of Henan Province and School of Physics and Electronics, Henan, University, Kaifeng 475001 (China); Li Shengjun, E-mail: lishengjun@hrbeu.edu.cn [Key Laboratory of Photovoltaic Materials of Henan Province and School of Physics and Electronics, Henan, University, Kaifeng 475001 (China)

2011-05-19

Highlights: > The electrochemical reduction of Zr(II)/Zr and Zr(IV)/Zr(II) were both proved to be diffusion-controlled process. > In the 773 K-973 K range, the diffusion coefficients of Zr(II) and Zr(IV) were determined: D{sub Zr(II)} = 0.15567exp{l_brace}-69.65 x 10{sup 3}RT(K){r_brace} cm{sup 2}/s, D{sub Zr(IV)} = 1.09 x 10{sup -4}exp{l_brace}-44.39 x 10{sup 3}RT(K){r_brace} cm{sup 2}/s. > The activation energy values for the diffusion process were 69.65 kJ/mol and 44.39 kJ/mol, respectively. > This investigation will be useful for the further cognition of the molten salt electrolysis of zirconium. - Abstract: The electroreduction process of Zr(IV) was studied at molybdenum electrode in LiCl-KCl-K{sub 2}ZrF{sub 6} molten salt. The transient electrochemical techniques, such as cyclic voltammetry and chronopotenimetry were used. The experimental results showed that the electrochemical reduction of Zr(II)/Zr and Zr(IV)/Zr(II) were both diffusion-controlled process. In the 773-973 K range, the diffusion coefficients of Zr(ii) and Zr(IV) were determined: D{sub Zr(II)} = 0.15567exp{l_brace}-69.65 x 10{sup 3}RT(K){r_brace} cm{sup 2}/s, D{sub Zr(IV)} = 1.09 x 10{sup -4} exp{l_brace}-44.39 x 10{sup 3}RT(K){r_brace} cm{sup 2}/s. The activation energy values for the diffusion process were 69.65 kJ/mol and 44.39 kJ/mol, respectively.

Six2 Is a Coordinator of LiCl-Induced Cell Proliferation and Apoptosis

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Jianing Liu

2016-09-01

Full Text Available The metanephric mesenchyme (MM cells are a subset of kidney progenitor cells and play an essential role in mesenchymal-epithelial transition (MET, the key step of nephron generation. Six2, a biological marker related to Wnt signaling pathway, promotes the proliferation, inhibits the apoptosis and maintains the un-differentiation of MM cells. Besides, LiCl is an activator of Wnt signaling pathway. However, the role of LiCl in cellular regulation of MM cells remains unclear, and the relationship between LiCl and Six2 in this process is also little known. Here, we performed EdU assay and flow cytometry assay to, respectively, detect the proliferation and apoptosis of MM cells treated with LiCl of increasing dosages. In addition, reverse transcription-PCR (RT-PCR and Western-blot were conducted to measure the expression of Six2 and some maker genes of Wnt and bone-morphogenetic-protein (BMP signaling pathway. Furthermore, luciferase assay was also carried out to detect the transcriptional regulation of Six2. Then we found LiCl promoted MM cell proliferation at low-concentration (10, 20, 30, and 40 mM. The expression of Six2 was dose-dependently increased in low-concentration (10, 20, 30, and 40 mM at both mRNA and protein level. In addition, both of cell proliferation and Six2 expression in MM cells declined when dosage reached high-concentration (50 mM. However, Six2 knock-down converted the proliferation reduction at 50 mM. Furthermore, Six2 deficiency increased the apoptosis of MM cells, compared with negative control cells at relative LiCl concentration. However, the abnormal rise of apoptosis at 30 mM of LiCl concentration implies that it might be the reduction of GSK3β that increased cell apoptosis. Together, these demonstrate that LiCl can induce the proliferation and apoptosis of MM cells coordinating with Six2.

Thermodynamics properties of plutonium in NaCl-KCl and CaCl{sub 2} at 1073 K and in liquid gallium

Energy Technology Data Exchange (ETDEWEB)

Lambertin, D.; Ched' homme, S.; Bourges, G.; Pescayre, L.; Sanchez, S.; Picard, G

2004-07-01

Cadmium and bismuth metal are mostly used as solvent in nuclear pyrochemical processes and especially in actinides/lanthanides separations. Gallium metal has been chosen because no literature values are available with plutonium and its regeneration by refining at low temperature is possible. Electrochemical window of gallium metal and activity coefficient of plutonium in gallium have been determined by using potentiometric method. Secondly, the electrochemical properties of plutonium have been studied in molten equimolar NaCl/KCl and CaCl{sub 2} at 1073 K by cyclic voltammetry. The standard potentials of Pu(III)/Pu redox couple, respectively, -2,54 V and -2,51 V, led to the calculation of the activity coefficients of Pu(III). In CaCl{sub 2} the complexation of Pu(III) ions is lower and the voltage gap between Pu(III)/Pu couple and the solvent limit is higher. The new data on plutonium electrochemistry in molten chlorides and liquid gallium media combined with literature data on lanthanides suggest that gallium can be a good solvent metal for pyro-chemistry separation. (authors)

Converting hcp Mg-Al-Zn alloy into bcc Mg-Li-Al-Zn alloy by electrolytic deposition and diffusion of reduced lithium atoms in a molten salt electrolyte LiCl-KCl

International Nuclear Information System (INIS)

Lin, M.C.; Tsai, C.Y.; Uan, J.Y.

2007-01-01

A body-centered cubic (bcc) Mg-12Li-9Al-1Zn (wt.%) alloy was fabricated in air by electrolysis from LiCl-KCl molten salt at 500 deg. C. Electrolytic deposition of Li atoms on cathode (Mg-Al-Zn alloy) and diffusion of the Li atoms formed the bcc Mg-Li-Al-Zn alloy with 12 wt.% Li and only 0.264 wt.% K. Low K concentration in the bcc Mg alloy strip after the electrolysis process resulted from 47% atomic size misfit between K and Mg atoms and low solubility of K in Mg matrix

Flexible electromagnetic wave sensor operating at GHz frequencies for instantaneous concentration measurements of NaCl, KCl, MnCl2 and CuCl solutions

International Nuclear Information System (INIS)

Korostynska, O; Ortoneda-Pedrola, M; Mason, A; Al-Shamma'a, A I

2014-01-01

A novel electromagnetic wave sensor operating at GHz frequencies for real-time chlorides concentration analysis is reported. The sensor response to deionized water, NaCl, KCl, MnCl 2  and CuCl solutions at various concentrations was tested. The sensing element, in the form of a silver pattern antenna that emits an electromagnetic field, was printed on a polyimide flexible laminate substrate to form a sensor to suit a broad range of applications, where a sensor could be placed in water reservoirs or fluid-carrying pipes for continuous analysis. The developed system confirmed the viability of using microwaves for real-time chloride solutions monitoring as the reflected signals represented by S 11  parameters were unique with clearly observed shifts in the resonant frequencies and amplitude changes when placed in direct contact with 20 µl of each solution. (paper)

Lithium chloride enhances bone regeneration and implant osseointegration in osteoporotic conditions.

Science.gov (United States)

Jin, Yifan; Xu, Lihua; Hu, Xiaohui; Liao, Shixian; Pathak, Janak L; Liu, Jinsong

2016-10-06

Osteoporotic patients have a high risk of dental and orthopedic implant failure. Lithium chloride (LiCl) has been reported to enhance bone formation. However, the role of LiCl in the success rate of dental and orthopedic implants in osteoporotic conditions is still unknown. We investigated whether LiCl enhances implant osseointegration, implant fixation, and bone formation in osteoporotic conditions. Sprague-Dawley female rats (n = 18) were ovariectomized (OVX) to induce osteoporosis, and another nine rats underwent sham surgery. Three months after surgery, titanium implants were implanted in the tibia of the OVX and sham group rats. After implantation, the OVX rats were gavaged with 150 mg/kg/2 days of LiCl (OVX + LiCl group) or saline (OVX group), and sham group rats were gavaged with saline for 3 months. Implant osseointegration and bone formation were analyzed using histology, biomechanical testing, and micro computed tomography (micro-CT). More bone loss was observed in the OVX group compared to the control, and LiCl treatment enhanced bone formation and implant fixation in osteoporotic rats. In the OVX group, bone-implant contact (BIC) was decreased by 81.2 % compared to the sham group. Interestingly, the OVX + LiCl group showed 4.4-fold higher BIC compared to the OVX group. Micro-CT data of tibia from the OVX + LiCl group showed higher bone volume, trabecular thickness, trabecular number, and osseointegration compared to the OVX group. Maximum push-out force and implant-bone interface shear strength were 2.9-fold stronger in the OVX + LiCl group compared to the OVX group. In conclusion, LiCl enhanced implant osseointegration, implant fixation, and bone formation in osteoporotic conditions, suggesting LiCl as a promising therapeutic agent to prevent implant failure and bone loss in osteoporotic conditions.

Enhancing effects of lithium on memory are not by-products of learning or attentional deficits.

Science.gov (United States)

Tsaltas, Eleftheria; Kyriazi, Theodora; Poulopoulou, Cornelia; Kontis, Dimitrios; Maillis, Antonios

2007-06-18

We recently reported that chronic lithium (LiCl), at therapeutic plasma levels, enhanced spatial working memory and retention of an aversive contingency. Here we examine the possibility that these effects be secondary to LiCl effects on the ability to ignore irrelevant stimuli or on fear conditioning. In Experiment 1, rats subjected to >30 daily intraperitoneal injections of LiCl (2mmol/kg) or saline underwent conditioned emotional response training (CER: 2 CS pairings with 1-s, 1-mA shock) after 40 pre-exposures either to the CS (latent inhibition-LiCl/latent inhibition-saline, n=8) or to another stimulus (control-LiCl/control-saline, n=8). In Experiment 2, eight LiCl and eight saline animals were trained in on-the-baseline (VI-60s) CER (1-s, 0.15-mA shock in CS-signalled periods) in the Skinner box. In Experiment 1, LiCl animals showed normal latent inhibition. In both experiments, their fear conditioning was unimpaired. Therefore, the previously reported memory improvement under chronic lithium cannot be attributed to changes in the ability to ignore irrelevant stimuli or in fear conditioning.

Fabrication of Ordered Nanopattern by using ABC Triblock Copolymer with Salt in Toluene.

Science.gov (United States)

Huang, Hailiang; Zhong, Benbin; Zu, Xihong; Luo, Hongsheng; Lin, Wenjing; Zhang, Minghai; Zhong, Yazhou; Yi, Guobin

2017-08-15

Ordered nanopatterns of triblock copolymer polystyrene-block-poly(2-vinylpyridine)-block- poly (ethylene oxide)(PS-b-P2VP-b-PEO) have been achieved by the addition of lithium chloride (LiCl). The morphological and structural evolution of PS-b-P2VP-b-PEO/LiCl thin films were systematically investigated by varying different experimental parameters, including the treatment for polymer solution after the addition of LiCl, the time scale of ultrasonic treatment and the molar ratio of Li + ions to the total number of oxygen atoms (O) in PEO block and the nitrogen atoms (N) in P2VP block. When toluene was used as the solvent for LiCl, ordered nanopattern with cylinders or nanostripes could be obtained after spin-coating. The mechanism of nanopattern transformation was related to the loading of LiCl in different microdomains.

The role of correlations in the determination of the transport properties of LaCl_3 in high temperature molten eutectic LiCl-KCl

International Nuclear Information System (INIS)

Samin, Adib; Wu, Evan; Zhang, Jinsuo

2017-01-01

It is important to develop an accurate assessment of fundamental data of lanthanides in high temperature molten salts to enable an efficient application of pyroprocessing. This requires a careful consideration of uncertainties in the reported results. In this study, cyclic voltammetry (CV) tests of LaCl_3 in KCl-LiCl molten salt were conducted at low concentration levels in the molten salt at 723 K and at several scan rates. The CV signals were subsequently analyzed through the conventional CV analysis and using a BET-based model through a nonlinear least-squares fitting procedure. It was determined that the parameters of the model were strongly correlated and the support plane procedure was implemented to assign joint confidence intervals for the diffusivity of lanthanum. Accounting for the correlations led to a significant increase in the uncertainty of the reported diffusivity which led to better agreement with the literature. Accounting for the correlations may be important for higher concentration levels.

Using a portable Raman spectrometer to detect carotenoids of halophilic prokaryotes in synthetic inclusions in NaCl, KCl, and sulfates.

Science.gov (United States)

Jehlička, Jan; Culka, Adam; Mana, Lilly; Oren, Aharon

2018-05-03

Cell suspensions of the haloarchaea Halorubrum sodomense and Halobacterium salinarum and the extremely halophilic bacterium Salinibacter ruber (Bacteroidetes) in saturated solutions of chlorides and sulfates (NaCl, KCl, MgSO 4 ·7H 2 O, K 2 SO 4 , and (NH 4 )Al(SO 4 ) 2 ·12H 2 O) were left to evaporate to produce micrometric inclusions in laboratory-grown crystals. Raman spectra of these pinkish inclusions were obtained using a handheld Raman spectrometer with green excitation (532 nm). This portable instrument does not include any microscopic tool. Acceptable Raman spectra of carotenoids were obtained in the range of 200-4000 cm -1 . This detection achievement was related to the mode of illumination and collection of scattered light as well as due to resonance Raman enhancement of carotenoid signals under green excitation. The position of diagnostic Raman carotenoid bands corresponds well to those specific carotenoids produced by a given halophile. To our best knowledge, this is the first study of carotenoids included in the laboratory in crystalline chlorides and sulfates, using a miniature portable Raman spectrometer. Graphical abstract ᅟ.

Influence of ionic strength in the adsorption and during photocatalysis of reactive black 5 azo dye on TiO{sub 2} coated on non woven paper with SiO{sub 2} as a binder

Energy Technology Data Exchange (ETDEWEB)

Aguedach, Abdelkahhar [Laboratoire de l' Eau et environnement, Universite Chouaib Doukkali, Faculte des Sciences, BP.20, El Jadida, Maroc (Morocco); Brosillon, Stephan [Laboratoire Science Chimiques de Rennes UMR 6226, Equipe Chimie et Ingenierie des Procedes, Ecole Nationale Superieure de Chimie, Universite Rennes 1, avenue du General Leclerc, 35700 Rennes (France)], E-mail: Stephan.Brosillon@ensc-rennes.fr; Morvan, Jean [Laboratoire Science Chimiques de Rennes UMR 6226, Equipe Chimie et Ingenierie des Procedes, Ecole Nationale Superieure de Chimie, Universite Rennes 1, avenue du General Leclerc, 35700 Rennes (France); Lhadi, El Kbir [Laboratoire de l' Eau et environnement, Universite Chouaib Doukkali, Faculte des Sciences, BP.20, El Jadida, Maroc (Morocco)

2008-01-31

Reactive black 5 (RB5), an azo dye, was degraded by using UV-irradiated TiO{sub 2} coated on non woven paper with SiO{sub 2} as a binder. The adsorption capacity of the photocatalyst was studied at natural pH, superior to pH{sub pzc} of the binder, for various ionic strengths. Different salts such as NaCl, KCl, CaCl{sub 2}, LiCl, Ca(NO{sub 3}){sub 2} were used to increase the ionic strength. The presence of salt increased the adsorption capacity. The electrostatic interactions between dye and oxide surface charges (TiO{sub 2}/SiO{sub 2}) is very important in the adsorption phenomena. The effect of the ionic strength of the solution on photocatalyst degradation was studied. The rate of degradation was increased by the presence of salts in the range of the experimental conditions. The increase of the initial decolorization rate was observed in the following order: Ca{sup 2+} > K{sup +} > Na{sup +} > Li{sup +}. Experiments with different anions (Cl{sup -}, NO{sub 3}{sup -}) had shown that nitrate was an indifferent electrolyte for the adsorption and photodegradation of the dye on SiO{sub 2}/TiO{sub 2}.

The use of additives for reducing hydrogen yield in mortar containing slag and chloride salts

International Nuclear Information System (INIS)

Lewis, M.A.; Warren, D.W.

1989-01-01

Cementitious waste forms are being considered for immobilizing nuclear waste before disposal. In earlier work, it was found that irradiation of a mortar formulation consisting of slag, portland cement, fly ash, water, and up to 10 wt% KCl endash LiCl salt resulted in the generation of hydrogen. Yields were relatively high and the rates of generation were constant for the irradiation period investigated. The addition of small amounts of oxygen-rich electron scavengers to the mortar was investigated as a means for reducing hydrogen yields. The addition of NaNO 3 reduced the hydrogen yield; changed the radiolytic products from hydrogen to a mixture of hydrogen, nitrogen, and N 2 O; and reduced the pressurization rate after exposure to 400 Mrads. The addition of NaIO 4 and KMnO 4 reduced hydrogen yields slightly while the addition of Ag 2 O increased the yield. Moreover, the addition of FeS to a non-slag mortar changed the radiolysis mechanism but the addition of FeO did not. The results of these experiments provided an insight into the nature of the radiolytic reactions occurring in the mortar formulations and indicated that the radiolytic generation of gases might be controlled with the proper choice of additive. 14 refs., 3 figs., 2 tabs

A view on thermodynamics of concentrated electrolytes: Modification necessity for electrostatic contribution of osmotic coefficient

Science.gov (United States)

Sahu, Jyoti; Juvekar, Vinay A.

2018-05-01

Prediction of the osmotic coefficient of concentrated electrolytes is needed in a wide variety of industrial applications. There is a need to correctly segregate the electrostatic contribution to osmotic coefficient from nonelectrostatic contribution. This is achieved in a rational way in this work. Using the Robinson-Stokes-Glueckauf hydrated ion model to predict non-electrostatic contribution to the osmotic coefficient, it is shown that hydration number should be independent of concentration so that the observed linear dependence of osmotic coefficient on electrolyte concentration in high concentration range could be predicted. The hydration number of several electrolytes (LiCl, NaCl, KCl, MgCl2, and MgSO4) has been estimated by this method. The hydration number predicted by this model shows correct dependence on temperature. It is also shown that the electrostatic contribution to osmotic coefficient is underpredicted by the Debye-Hückel theory at concentration beyond 0.1 m. The Debye-Hückel theory is modified by introducing a concentration dependent hydrated ionic size. Using the present analysis, it is possible to correctly estimate the electrostatic contribution to the osmotic coefficient, beyond the range of validation of the D-H theory. This would allow development of a more fundamental model for electrostatic interaction at high electrolyte concentrations.

Separation and Recovery of Uranium Metal from Spent Light Water Reactor Fuel via Electrolytic Reduction and Electrorefining

International Nuclear Information System (INIS)

Herrmann, S.D.; Li, S.X.

2010-01-01

A series of bench-scale experiments was performed in a hot cell at Idaho National Laboratory to demonstrate the separation and recovery of uranium metal from spent light water reactor (LWR) oxide fuel. The experiments involved crushing spent LWR fuel to particulate and separating it from its cladding. Oxide fuel particulate was then converted to metal in a series of six electrolytic reduction runs that were performed in succession with a single salt loading of molten LiCl - 1 wt% Li2O at 650 C. Analysis of salt samples following the series of electrolytic reduction runs identified the diffusion of select fission products from the spent fuel to the molten salt electrolyte. The extents of metal oxide conversion in the post-test fuel were also quantified, including a nominal 99.7% conversion of uranium oxide to metal. Uranium metal was then separated from the reduced LWR fuel in a series of six electrorefining runs that were performed in succession with a single salt loading of molten LiCl-KCl-UCl3 at 500 C. Analysis of salt samples following the series of electrorefining runs identified additional partitioning of fission products into the molten salt electrolyte. Analyses of the separated uranium metal were performed, and its decontamination factors were determined.

Over-expression of TaMYB33 encoding a novel wheat MYB transcription factor increases salt and drought tolerance in Arabidopsis.

Science.gov (United States)

Qin, Yuxiang; Wang, Mengcheng; Tian, Yanchen; He, Wenxing; Han, Lu; Xia, Guangmin

2012-06-01

Salt and drought stresses often adversely affect plant growth and productivity, MYB transcription factors have been shown to participate in the response to these stresses. Here we identified a new R2R3-type MYB transcription factor gene TaMYB33 from wheat (Triticum aestivum). TaMYB33 was induced by NaCl, PEG and ABA treatments, and its promoter sequence contains putative ABRE, MYB and other abiotic stress related cis-elements. Ectopic over-expression of TaMYB33 in Arabidopsis thaliana remarkably enhanced its tolerance to drought and NaCl stresses, but not to LiCl and KCl treatments. The expressions of AtP5CS and AtZAT12 which mirror the activities of proline and ascorbate peroxidase synthesis respectively were induced in TaMYB33 over-expression lines, indicating TaMYB33 promotes the ability for osmotic pressure balance-reconstruction and reactive oxidative species (ROS) scavenging. The up-regulation of AtAAO3 along with down-regulation of AtABF3, AtABI1 in TaMYB33 over-expression lines indicated that ABA synthesis was elevated while its signaling was restricted. These results suggest that TaMYB33 enhances salt and drought tolerance partially through superior ability for osmotic balance reconstruction and ROS detoxification.

Analysis of electron pair production in the collision system Ar+KCl at 1.76 AGeV; Analyse der Elektronpaarproduktion im Stosssystem Ar+KCl bei 1,76 AGeV

Energy Technology Data Exchange (ETDEWEB)

Lang, Simon Martin

2008-06-30

The HADES-spectrometer at GSI is used to measure the production of the light vector mesons {rho}, {omega} and {phi} at SIS energies. Therefore, the medium sized collision system Ar+KCl was measured at 1.76 AGeV kinetic energy of beam particles. In this system the density of particle tracks is much larger as compared to the formerly used collision system C+C, making it necessary to upgrade the data analysis. The previous method of hard-cuts - used for particle identification - was replaced by a newly developed multi-variate analysis based on an artificial neural network. This algorithm has the benefit, that it is more robust against fluctuations in one or more of the used detector observables. This increases the overall efficiency and purity of the analysis procedure. Furthermore, the reconstruction of particle tracks inside the HADES spectrometer is based on a few position information, only. During analysis of raw data, these information are combined to a artificially large manifold of tracks. This leads to the general problem that one has to select the maximum number of true physical tracks out of this set of tracks per event. A new method of track selection is used to filter the data not only to select single tracks, but also to identify electron pairs created during Dalitz-decay of {pi}{sup 0} mesons, which build the bulk of combinatorial background. The result of the analysis is an efficiency corrected invariant mass spectrum of electron pairs, normalized to the mean number of pions per event. The spectrum consists of more than 16,000 pairs with an invariant mass larger than 150 MeV. In total more than 150000 pairs were found. A first comparison with the spectra calculated by using the old analysis approach shows a 30% enhancement in yield of reconstructed electron pairs. A first comparison with a simple thermal model implemented by the Pluto event generator, opens the possibility to compare the measured pair yield of {omega} and {phi} mesons via m{sub T

X-ray diffraction studies of structures of Be, Al, LiF, Fe+3%Si, Si, SiO2, KCl under dynamic pressures from 2 Gpa to 20 Gpa

International Nuclear Information System (INIS)

Egorov, L.A.; Barenboim, A.I.; Mokhova, V.V.; Dorohin, V.V.; Samoilov, A.I.

1997-01-01

Currently, the only direct method to study behaviour of solid crystal substance structures under dynamic compression is method to record X-rays diffraction pictures of crystal structures under shock compression. Thepaper presents results of X-rays diffraction measurements concerning structural parameters of shock compressed substances at pressures higher than Hugoniot elastic limit (Be, Al, LiF, Fe+3%Si), lower than Hugoniot elastic limit (Si, SiO 2 , LiF) and in the area of pressures of phase transformation beginning (KCl, Si). Recorded states of shock-compressed substance structures demonstrate identity of structural deformations at pressures higher and lower than Hugoniot elastic limit as well as at pressures above the phase transformation point, which can be characterized as single-axial deformations. (orig.)

Rapid, labile, and protein synthesis-independent short-term memory in conditioned taste aversion.

Science.gov (United States)

Houpt, T A; Berlin, R

1999-01-01

Short-term memory is a rapid, labile, and protein-synthesis-independent phase of memory. The existence of short-term memory in conditioned taste aversion (CTA) learning has not been demonstrated formally. To determine the earliest time at which a CTA is expressed, we measured intraoral intake of sucrose at 15 min, 1 hr, 6 hr, or 48 h after contingent pairing of an intraoral infusion of 5% sucrose (6.6 ml over 6 min) and toxic lithium chloride injection (76 mg/kg). Rats were implanted with intraoral catheters to allow presentation of taste solutions at arbitrary times. Intraoral intake was measured under conditions of long-delay, single-trial learning typical of CTA. Rats decreased intraoral intake of sucrose at 15 min after contingent pairing of sucrose and LiCl, but not after noncontingent LiCl or sucrose. Thus CTA learning can be expressed rapidly. To determine if short-term CTA memory is labile and decays in the absence of long-term memory, we measured intraoral intake of sucrose after pairing sucrose with low doses of LiCl. Rats received an intraoral infusion of 5% sucrose (6 ml/6 min); 30 min later LiCl was injected at three different doses (19, 38, or 76 mg/kg). A second intraoral infusion of sucrose was administered 15 min, 1 hr, 3 hr, 4.5 hr, 6 hr, or 48 hr later. The formation of long-term CTA memory was dependent on the dose of LiCl paired with sucrose during acquisition. Low doses of LiCl induced a CTA that decayed within 6 hr after pairing. Central administration of the protein synthesis inhibitor cycloheximide prior to LiCl injection blocked long-term CTA expression at 6 and 48 hr, but not short-term CTA expression at 1 hr. Thus, short-term memory for CTA learning exists that is acquired rapidly and independent of protein synthesis, but labile in the absence of long-term memory formation.

The role of correlations in the determination of the transport properties of LaCl{sub 3} in high temperature molten eutectic LiCl-KCl

Energy Technology Data Exchange (ETDEWEB)

Samin, Adib; Wu, Evan; Zhang, Jinsuo [The Ohio State Univ., Columbus, OH (United States). Dept. of Mechanical and Aerospace Engineering

2017-10-01

It is important to develop an accurate assessment of fundamental data of lanthanides in high temperature molten salts to enable an efficient application of pyroprocessing. This requires a careful consideration of uncertainties in the reported results. In this study, cyclic voltammetry (CV) tests of LaCl{sub 3} in KCl-LiCl molten salt were conducted at low concentration levels in the molten salt at 723 K and at several scan rates. The CV signals were subsequently analyzed through the conventional CV analysis and using a BET-based model through a nonlinear least-squares fitting procedure. It was determined that the parameters of the model were strongly correlated and the support plane procedure was implemented to assign joint confidence intervals for the diffusivity of lanthanum. Accounting for the correlations led to a significant increase in the uncertainty of the reported diffusivity which led to better agreement with the literature. Accounting for the correlations may be important for higher concentration levels.

Studies on the Electrochemical Dissolution for the Treatment of 10 g-Scale Zircaloy-4 Cladding Hull Wastes in LiCl-KCl Molten Salts

International Nuclear Information System (INIS)

Lee, You Lee; Lee, Jang Hwa; Jeon, Min Ku; Kang, Kweon Ho

2012-01-01

The electrochemical behaviors of 10 g-scale fresh and oxidized Zircaloy-4 cladding hulls were examined in 500 degree C LiCl-KCl molten salts to confirm the feasibility of the electrorefining process for the treatment of hull wastes. In the results of measuring the potential-current response using a stainless steel basket filled with oxidized Zircaloy-4 hull specimens, the oxidation peak of Zr appears to be at -0.7 to -0.8 V vs. Ag/AgCl, which is similar to that of fresh Zircaloy-4 hulls, while the oxidation current is found to be much smaller than that of fresh Zircaloy-4 hulls. These results are congruent with the outcome of current-time curves at -0.78 V and of measuring the change in the average weight and thickness after the electrochemical dissolution process. Although the oxide layer on the surface affects the uniformity and rate of dissolution by decreasing the conductivity of Zircaloy-4 hulls, electrochemical dissolution is considered to occur owing to the defect of the surface and phase properties of the Zr oxide layer.

Electrical Conductivity of Molten DyCl3-NaCl and DyCl3-KCl Systems: An Approach to Structural Interpretations of Rare Earth Chloride Melts

Science.gov (United States)

Iwadate, Yasuhiko; Ohkubo, Takahiro

2017-11-01

Electrical conductivities (κs) of molten DyCl3-NaCl and DyCl3-KCl systems were estimated by measuring the impedances of each mixture melt at any temperature and/or frequency. The molar volumes (Vms) were measured by dilatometry and represented as a polynomial empirical equation of temperature and composition. Due to both the properties, the molar conductivities (Λms) were calculated and their temperature and/or composition dependences were discussed from the standpoint of structural features as well. The κs increased curvilinearly with increasing temperature across the whole composition ranges. This trend was also applied to the Λms which was fitted by an Arrhenius-type equation. The relationship of Λms with melt composition was studied and the Λms were found to decrease with increasing composition of DyCl3. These findings were interpreted based on the results of structural science so far reported, and finally, the relationship between Λms and the structures of pure rare earth chloride melts was discussed.

Isotope effect in enthalpy of solvation of the lithium ion

International Nuclear Information System (INIS)

Krestov, G.A.; Egorov, G.I.; Korolev, V.P.

1989-01-01

At 298.15 K, the authors determined the standard enthalpies of solution for 6 LiCl and 7 LiCl in water, heavy water, dimethylsulfoxide (DMSO) and aqueous solutions of DMSO. The authors have established that solvation of 6 Li + is differentiated in water and DMSO to a greater degree than for 7 Li +

Automated Potentiometric Titrations in KCl/Water-Saturated Octanol: Method for Quantifying Factors Influencing Ion-Pair Partitioning

Science.gov (United States)

2009-01-01

The knowledge base of factors influencing ion pair partitioning is very sparse, primarily because of the difficulty in determining accurate log PI values of desirable low molecular weight (MW) reference compounds. We have developed a potentiometric titration procedure in KCl/water-saturated octanol that provides a link to log PI through the thermodynamic cycle of ionization and partitioning. These titrations have the advantage of being independent of the magnitude of log P, while maintaining a reproducibility of a few hundredths of a log P in the calculated difference between log P neutral and log P ion pair (diff (log PN − I)). Simple model compounds can be used. The titration procedure is described in detail, along with a program for calculating pKa′′ values incorporating the ionization of water in octanol. Hydrogen bonding and steric factors have a greater influence on ion pairs than they do on neutral species, yet these factors are missing from current programs used to calculate log PI and log D. In contrast to the common assumption that diff (log PN − I) is the same for all amines, they can actually vary more than 3 log units, as in our examples. A major factor affecting log PI is the ability of water and the counterion to approach the charge center. Bulky substituents near the charge center have a negative influence on log PI. On the other hand, hydrogen bonding groups near the charge center have the opposite effect by lowering the free energy of the ion pair. The use of this titration method to determine substituent ion pair stabilization values (IPS) should bring about more accurate log D calculations and encourage species-specific QSAR involving log DN and log DI. This work also brings attention to the fascinating world of nature’s highly stabilized ion pairs. PMID:19265385

Automated potentiometric titrations in KCl/water-saturated octanol: method for quantifying factors influencing ion-pair partitioning.

Science.gov (United States)

Scherrer, Robert A; Donovan, Stephen F

2009-04-01

The knowledge base of factors influencing ion pair partitioning is very sparse, primarily because of the difficulty in determining accurate log P(I) values of desirable low molecular weight (MW) reference compounds. We have developed a potentiometric titration procedure in KCl/water-saturated octanol that provides a link to log P(I) through the thermodynamic cycle of ionization and partitioning. These titrations have the advantage of being independent of the magnitude of log P, while maintaining a reproducibility of a few hundredths of a log P in the calculated difference between log P neutral and log P ion pair (diff (log P(N - I))). Simple model compounds can be used. The titration procedure is described in detail, along with a program for calculating pK(a)'' values incorporating the ionization of water in octanol. Hydrogen bonding and steric factors have a greater influence on ion pairs than they do on neutral species, yet these factors are missing from current programs used to calculate log P(I) and log D. In contrast to the common assumption that diff (log P(N - I)) is the same for all amines, they can actually vary more than 3 log units, as in our examples. A major factor affecting log P(I) is the ability of water and the counterion to approach the charge center. Bulky substituents near the charge center have a negative influence on log P(I). On the other hand, hydrogen bonding groups near the charge center have the opposite effect by lowering the free energy of the ion pair. The use of this titration method to determine substituent ion pair stabilization values (IPS) should bring about more accurate log D calculations and encourage species-specific QSAR involving log D(N) and log D(I). This work also brings attention to the fascinating world of nature's highly stabilized ion pairs.

Combined application of arsenic trioxide and lithium chloride augments viability reduction and apoptosis induction in human rhabdomyosarcoma cell lines.

Directory of Open Access Journals (Sweden)

Sabine B Schleicher

Full Text Available Rhabdomyosarcomas (RMS are the most prevalent soft tissue sarcomas affecting children and adolescents. Despite intensive treatment consisting of multimodal chemotherapy and surgery RMS patients diagnosed with metastatic disease expect long term survival rates of only 20%. Often multidrug resistance arises upon initial response emphasizing the need for new therapeutic drugs to improve treatment efficiency. Previously, we demonstrated the efficacy of the FDA approved drug arsenic trioxide (ATO specifically inhibiting viability and clonal growth as well as inducing cell death in human RMS cell lines of different subtypes. In this study, we combined low dose ATO with lithium chloride (LiCl, which is approved as mood stabilizer for the treatment of bipolar disorder, but also inhibits growth and survival of different cancer cell types in pre-clinical research. Indeed, we could show additive effects of LiCl and ATO on viability reduction, decrease of colony formation as well as cell death induction. In the course of this, LiCl induced inhibitory glycogen synthase kinase-3β (GSK-3β serine 9 phosphorylation, whereas glioma associated oncogene family 1 (GLI1 protein expression was particularly reduced by combined ATO and LiCl treatment in RD and RH-30 cell lines, showing high rates of apoptotic cell death. These results imply that combination of ATO with LiCl or another drug targeting GSK-3 is a promising strategy to enforce the treatment efficiency in resistant and recurrent RMS.

Regulated phosphorylation of the K-Cl cotransporter KCC3 is a molecular switch of intracellular potassium content and cell volume homeostasis.

Science.gov (United States)

Adragna, Norma C; Ravilla, Nagendra B; Lauf, Peter K; Begum, Gulnaz; Khanna, Arjun R; Sun, Dandan; Kahle, Kristopher T

2015-01-01

The defense of cell volume against excessive shrinkage or swelling is a requirement for cell function and organismal survival. Cell swelling triggers a coordinated homeostatic response termed regulatory volume decrease (RVD), resulting in K(+) and Cl(-) efflux via activation of K(+) channels, volume-regulated anion channels (VRACs), and the K(+)-Cl(-) cotransporters, including KCC3. Here, we show genetic alanine (Ala) substitution at threonines (Thr) 991 and 1048 in the KCC3a isoform carboxyl-terminus, preventing inhibitory phosphorylation at these sites, not only significantly up-regulates KCC3a activity up to 25-fold in normally inhibitory isotonic conditions, but is also accompanied by reversal of activity of the related bumetanide-sensitive Na(+)-K(+)-2Cl(-) cotransporter isoform 1 (NKCC1). This results in a rapid (90%) reduction in intracellular K(+) content (Ki) via both Cl-dependent (KCC3a + NKCC1) and Cl-independent [DCPIB (VRAC inhibitor)-sensitive] pathways, which collectively renders cells less prone to acute swelling in hypotonic osmotic stress. Together, these data demonstrate the phosphorylation state of Thr991/Thr1048 in KCC3a encodes a potent switch of transporter activity, Ki homeostasis, and cell volume regulation, and reveal novel observations into the functional interaction among ion transport molecules involved in RVD.

Experimental Study of Codeposition Electrochemistry Using Mixtures of ScCl₃ and YCl₃ in LiCl-KCl Eutectic Salt at 500°C

Energy Technology Data Exchange (ETDEWEB)

Shaltry, Michael R. [Idaho National Lab. (INL), Idaho Falls, ID (United States); Yoo, Tae-Sic [Idaho National Lab. (INL), Idaho Falls, ID (United States); Fredrickson, Guy L. [Idaho National Lab. (INL), Idaho Falls, ID (United States)

2017-09-12

Cyclic voltammetry and chronopotentiometry tests were applied to molten LiCl-KCl eutectic at 500 °C including amounts of ScCl₃ and YCl₃. The purpose of the testing was to observe the effect of applied electrical current on the codeposition of scandium and yttrium, which were chosen as surrogate elements for uranium and plutonium, respectively. Features of the work were to vary the concentration of ScCl₃ (at relatively low concentrations) as well as varying the applied current, all with a fixed concentration of YCl₃. Results of the experiments could provide insight of uranium electrorefining and may provide evidence, which suggests the electrorefiner could be operated at lower UCl₃ concentration whereby codeposition (U and Pu) could be more effectively controlled.

A calorimetric method to determine water activity.

Science.gov (United States)

Björklund, Sebastian; Wadsö, Lars

2011-11-01

A calorimetric method to determine water activity covering the full range of the water activity scale is presented. A dry stream of nitrogen gas is passed either over the solution whose activity should be determined or left dry before it is saturated by bubbling through water in an isothermal calorimeter. The unknown activity is in principle determined by comparing the thermal power of vaporization related to the gas stream with unknown activity to that with zero activity. Except for three minor corrections (for pressure drop, non-perfect humidification, and evaporative cooling) the unknown water activity is calculated solely based on the water activity end-points zero and unity. Thus, there is no need for calibration with references with known water activities. The method has been evaluated at 30 °C by measuring the water activity of seven aqueous sodium chloride solutions ranging from 0.1 mol kg(-1) to 3 mol kg(-1) and seven saturated aqueous salt solutions (LiCl, MgCl(2), NaBr, NaCl, KCl, KNO(3), and K(2)SO(4)) with known water activities. The performance of the method was adequate over the complete water activity scale. At high water activities the performance was excellent, which is encouraging as many other methods used for water activity determination have limited performance at high water activities. © 2011 American Institute of Physics

Nebulizer calibration using lithium chloride: an accurate, reproducible and user-friendly method.

Science.gov (United States)

Ward, R J; Reid, D W; Leonard, R F; Johns, D P; Walters, E H

1998-04-01

Conventional gravimetric (weight loss) calibration of jet nebulizers overestimates their aerosol output by up to 80% due to unaccounted evaporative loss. We examined two methods of measuring true aerosol output from jet nebulizers. A new adaptation of a widely available clinical assay for lithium (determined by flame photometry, LiCl method) was compared to an existing electrochemical method based on fluoride detection (NaF method). The agreement between the two methods and the repeatability of each method were examined. Ten Mefar jet nebulizers were studied using a Mefar MK3 inhalation dosimeter. There was no significant difference between the two methods (p=0.76) with mean aerosol output of the 10 nebulizers being 7.40 mg x s(-1) (SD 1.06; range 5.86-9.36 mg x s(-1)) for the NaF method and 7.27 mg x s(-1) (SD 0.82; range 5.52-8.26 mg x s(-1)) for the LiCl method. The LiCl method had a coefficient of repeatability of 13 mg x s(-1) compared with 3.7 mg x s(-1) for the NaF method. The LiCl method accurately measured true aerosol output and was considerably easier to use. It was also more repeatable, and hence more precise, than the NaF method. Because the LiCl method uses an assay that is routinely available from hospital biochemistry laboratories, it is easy to use and, thus, can readily be adopted by busy respiratory function departments.

Residual Salt Separation from the Metal Products Reduced in a LiCl-Li2O Molten Salt

International Nuclear Information System (INIS)

Hur, Jin Mok; Hong, Sun Seok; Kang, Dae Seung; Jeong, Meong Soo; Seo, Chung Seok

2006-02-01

The electrochemical reduction of spent nuclear fuel in a LiCl-Li 2 O molten salt for the conditioning of spent nuclear fuel requires the separation of the residual salts from a reduced metal product after the reduction process. Considering the behavior of spent nuclear fuel during the electrochemical reduction process, a surrogate material matrix was constructed and inactive tests on a salt separation were carried out to produce the data required for the active tests. Fresh uranium metal prepared from the electrochemical reduction of U 3 O 8 powder was used as the surrogates of the spent nuclear fuel components which might be metallized by the electrochemical reduction process. LiCl, Li 2 O, Y 2 O 3 and SrCl 2 were selected as the components of the residual salts. Interactions between the salts and their influence on the separation of the residual salts were analyzed by differential scanning calorimetry (DSC) and thermogravimetry (TG). Eutectic melting of LiCl-Li 2 O and LiCl-SrCl 2 led to a melting point which was lower than that of a LiCl molten salt was observed. Residual salts were separated by a vaporization method. Co-vaporization of LiCl-Li 2 O and LiCl-SrCl 2 was achieved below temperatures which could make the uranium metal oxidation by Li 2 O possible. The salt vaporization rates at 950 .deg. C were measured as follows: LiCl-8 wt% Li 2 O > LiCl > LiCl-8 wt% SrCl 2 > SrCl 2

Characterization of incomplete fusion in the reactions Ar + KCl at 32,40,52 and 74 MeV/u; Caracterisation de la fusion incomplete dans les reactions Ar + KCl a 32,40,52 et 74 Mev/u

Energy Technology Data Exchange (ETDEWEB)

Bisquer, E [Lyon-1 Univ., 69 - Villeurbanne (France). Inst. de Physique Nucleaire; [Universite Claude Bernard, 69 - Lyon (France)

1996-12-20

Heavy ion collisions at intermediate energies (10 to 100 A.MeV) have been investigated and gave evidence to the persistence of so-called low energy mechanisms such as incomplete fusion. This thesis aims at determining the energy threshold beyond which such a mechanism does not occur any more. First we investigated the so-called conventional incomplete fusion. This mechanism is well known from low energy studies: a thermalized compound nucleus is formed which further de-excites by evaporating particles. Residues will be therefore detected in coincidence with mainly light particles. Ar + KCl at incident energies of 32, 40, 52 and 74 A.MeV has been selected for this analysis. These experiments have been performed using the INDRA multidetector in GANIL (Caen). The detection performance of INDRA allowed to use new analysis methods via global variables. In a first step, global variables have been compared in order to find the one that is the most appropriate to our study. Then incomplete fusion events have been extracted from raw events recorded at incident energies of 32, 40 and 52 A.MeV. It turned out that the contribution of this mechanisms was very weak at 52. A.MeV. It turned out that the contribution of this mechanism was very weak at 52 A.MeV and even zero at 74 A.MeV. We then investigated events in which three fragments were detected which could possibly sign multifragmentation. We did not find instantaneous multifragmentation with any expansion contribution. We also performed BNV simulations in order to compare our experimental results to model predictions, solving in a semi-classical way the Vlasov transport equation. A good agreement has been obtained on the size of the compound nucleus formed. However the excitation energy has not been reproduced, as the code seems to overestimate the energy taken away by preequilibrium particles. Incomplete fusion decreases as a function of energy but is not replaced by instantaneous multifragmentation with any expansion

Studies of the effects of TiCl3 in LiBH4/CaH2/TiCl3 reversible hydrogen storage system

International Nuclear Information System (INIS)

Liu Dongan; Yang Jun; Ni Jun; Drews, Andy

2012-01-01

Highlights: ► We systematically studied the effects of TiCl 3 in LiBH 4 /CaH 2 /TiCl 3 hydrogen storage system. ► It is found that adding 0.25 TiCl 3 produces fully reversible hydrogen absorption and desorption and a lower desorption temperature. ► LiCl experiences four different states, i.e. “formed-solid solution-molten solution-precipitation”, in the whole desorption process of the system. ► The incorporation of LiCl into LiBH 4 forms more viscous molten LiBH 4 ·LiCl, leading to fast kinetics. ► The precipitation and re-incorporation of LiCl into LiBH 4 lead to a fully reversible complex hydrogen storage system. - Abstract: In the present study, the effects of TiCl 3 on desorption kinetics, absorption/desorption reversibility, and related phase transformation processes in LiBH 4 /CaH 2 /TiCl 3 hydrogen storage system was studied systematically by varying its concentration (x = 0, 0.05, 0.15 and 0.25). The results show that LiCl forms during ball milling of 6LiBH 4 /CaH 2 /xTiCl 3 and that as temperature increases, o-LiBH 4 transforms into h-LiBH 4 , into which LiCl incorporates, forming solid solution of LiBH 4 ·LiCl, which melts above 280 °C. Molten LiBH 4 ·LiCl is more viscous than molten LiBH 4 , preventing the clustering of LiBH 4 and the accompanied agglomeration of CaH 2 , and thus preserving the nano-sized phase arrangement formed during ball milling. Above 350 °C, the molten solution LiBH 4 ·LiCl further reacts with CaH 2 , precipitating LiCl. The main hydrogen desorption reaction is between molten LiBH 4 ·LiCl and CaH 2 and not between molten LiBH 4 and CaH 2 . This alters the hydrogen reaction thermodynamics and lowers the hydrogen desorption temperature. In addition, the solid–liquid nano-sized phase arrangement in the nano-composites improves the hydrogen reaction kinetics. The reversible incorporation/precipitation of LiCl at the hydrogen reaction temperature and during temperature cycling makes the 6LiBH 4 /CaH 2 /0.25TiCl 3

Electrochemical studies and analysis of 1–10 wt% UCl3 concentrations in molten LiCl–KCl eutectic

International Nuclear Information System (INIS)

Hoover, Robert O.; Shaltry, Michael R.; Martin, Sean; Sridharan, Kumar; Phongikaroon, Supathorn

2014-01-01

Three electrochemical methods – cyclic voltammetry (CV), chronopotentiometry (CP), and anodic stripping voltammetry (ASV) – were applied to solutions of up to 10 wt% UCl 3 in the molten LiCl–KCl eutectic salt at 500 °C to determine electrochemical properties and behaviors and to help provide a scientific basis for the development of an in situ electrochemical probe for determining the concentration of uranium in a used nuclear fuel electrorefiner. Diffusion coefficients of UCl 4 and UCl 3 were calculated to be (6.72 ± 0.360) × 10 −6 cm 2 /s and (1.04 ± 0.17) × 10 −5 cm 2 /s, respectively. Apparent standard reduction potentials were determined to be (−0.381 ± 0.013) V and (−1.502 ± 0.076) V vs. 5 mol% Ag/AgCl or (−1.448 ± 0.013) V and (−2.568 ± 0.076) V vs. Cl 2 /Cl − for the U(IV)/U(III) and U(III)/U redox couples, respectively. In comparing this data with supercooled thermodynamic data to determine activity coefficients, the thermodynamic database used was important with resulting activity coefficients ranging from 2.34 × 10 −3 to 1.08 × 10 −2 for UCl 4 and 4.94 × 10 −5 to 4.50 × 10 −4 for UCl 3 . Of anodic stripping voltammetry and cyclic voltammetry anodic or cathodic peaks, the CV cathodic peak height divided by square root of scan rate was shown to be the most reliable method of determining UCl 3 concentration in the molten salt

K-Cl Cotransporter 2-mediated Cl- Extrusion Determines Developmental Stage-dependent Impact of Propofol Anesthesia on Dendritic Spines.

Science.gov (United States)

Puskarjov, Martin; Fiumelli, Hubert; Briner, Adrian; Bodogan, Timea; Demeter, Kornel; Lacoh, Claudia-Marvine; Mavrovic, Martina; Blaesse, Peter; Kaila, Kai; Vutskits, Laszlo

2017-05-01

General anesthetics potentiating γ-aminobutyric acid (GABA)-mediated signaling are known to induce a persistent decrement in excitatory synapse number in the cerebral cortex when applied during early postnatal development, while an opposite action is produced at later stages. Here, the authors test the hypothesis that the effect of general anesthetics on synaptogenesis depends upon the efficacy of GABA receptor type A (GABAA)-mediated inhibition controlled by the developmental up-regulation of the potassium-chloride (K-Cl) cotransporter 2 (KCC2). In utero electroporation of KCC2 was used to prematurely increase the efficacy of (GABAA)-mediated inhibition in layer 2/3 pyramidal neurons in the immature rat somatosensory cortex. Parallel experiments with expression of the inward-rectifier potassium channel Kir2.1 were done to reduce intrinsic neuronal excitability. The effects of these genetic manipulations (n = 3 to 4 animals per experimental group) were evaluated using iontophoretic injection of Lucifer Yellow (n = 8 to 12 cells per animal). The total number of spines analyzed per group ranged between 907 and 3,371. The authors found a robust effect of the developmental up-regulation of KCC2-mediated Cl transport on the age-dependent action of propofol on dendritic spines. Premature expression of KCC2, unlike expression of a transport-inactive KCC2 variant, prevented a propofol-induced decrease in spine density. In line with a reduction in neuronal excitability, the above result was qualitatively replicated by overexpression of Kir2.1. The KCC2-dependent developmental increase in the efficacy of GABAA-mediated inhibition is a major determinant of the age-dependent actions of propofol on dendritic spinogenesis.

Uranium isotopic composition and uranium concentration in special reference material SRM A (uranium in KCl/LiCl salt matrix)

International Nuclear Information System (INIS)

Graczyk, D.G.; Essling, A.M.; Sabau, C.S.; Smith, F.P.; Bowers, D.L.; Ackerman, J.P.

1997-07-01

To help assure that analysis data of known quality will be produced in support of demonstration programs at the Fuel Conditioning Facility at Argonne National Laboratory-West (Idaho Falls, ID), a special reference material has been prepared and characterized. Designated SRM A, the material consists of individual units of LiCl/KCl eutectic salt containing a nominal concentration of 2.5 wt. % enriched uranium. Analyses were performed at Argonne National Laboratory-East (Argonne, IL) to determine the uniformity of the material and to establish reference values for the uranium concentration and uranium isotopic composition. Ten units from a batch of approximately 190 units were analyzed by the mass spectrometric isotope dilution technique to determine their uranium concentration. These measurements provided a mean value of 2.5058 ± 0.0052 wt. % U, where the uncertainty includes estimated limits to both random and systematic errors that might have affected the measurements. Evidence was found of a small, apparently random, non-uniformity in uranium content of the individual SRM A units, which exhibits a standard deviation of 0.078% of the mean uranium concentration. Isotopic analysis of the uranium from three units, by means of thermal ionization mass spectrometry with a special, internal-standard procedure, indicated that the uranium isotopy is uniform among the pellets with a composition corresponding to 0.1115 ± 0.0006 wt. % 234 U, 19.8336 ± 0.0059 wt. % 235 U, 0.1337 ± 0.0006 wt. % 236 U, and 79.9171 ± 0.0057 wt. % 238 U

Stabilization/Solidification of Radioactive LiCl-KCl Waste Salt by Using SiO2-Al2O3-P2O5(SAP) Inorganic Composite: Part 2. The Effect of SAP Composition on Stabilization/Solidification

International Nuclear Information System (INIS)

Ahn, Soo Na; Park, Hwan Seo; Cho, In Hak; Kim, In Tae; Cho, Yong Zun

2012-01-01

Metal chloride waste is generated as a main waste streams in a series of electrolytic processes of a pyrochemical process. Different from carbonate or nitrate salt, metal chloride is not decomposed into oxide and chlorine but it is just vaporized. Also, it has low compatibility with conventional silicate glasses. Our research group adapted the dechlorination approach for the immobilization of waste salt. In this study, the composition of SAP (SiO 2 -Al 2 O 3 -P 2 O 5 ) was adjusted to enhance the reactivity and to simplify the solidification process as a subsequent research. The addition of Fe 2 O 3 into the basic SAP decreased the SAP/Salt ratio in weight from 3 for SAP 1071 to 2.25 for M-SAP(Fe=0.1). The experimental results indicated that the addition of Fe 2 O 3 increased the reactivity of M-SAP with LiCl-KCl but the reactivity gradually decreased above Fe=0.1. Also, introducing B 2 O 3 into M-SAP requires no glass binder for the consolidation of reaction products. U-SAP (SiO 2 -Al 2 O 3 -P 2 O 5 ) could effectively dechlorinate the LiCl-KCl waste and its reaction product could be consolidated as a monolithic form without a glass binder. The leaching test result indicated that U-SAP 1071 was more durable than other SAPs wasteform. By using U-SAP, 1 g of waste salt could generated 3 - 4 g of wasteform for final disposal. The final volume would be about 3 - 4 times lower than the glass-bonded sodalite. From these results, it could be concluded that the dechlorination approach using U-SAP would be one of prospective methods to manage the volatile waste salt.

Determination of activity coefficient of lanthanum chloride in molten LiCl-KCl eutectic salt as a function of cesium chloride and lanthanum chloride concentrations using electromotive force measurements

Energy Technology Data Exchange (ETDEWEB)

Bagri, Prashant, E-mail: prashant.bagri@utah.edu; Simpson, Michael F.

2016-12-15

The thermodynamic behavior of lanthanides in molten salt systems is of significant scientific interest for the spent fuel reprocessing of Generation IV reactors. In this study, the apparent standard reduction potential (apparent potential) and activity coefficient of LaCl{sub 3} were determined in a molten salt solution of eutectic LiCl-KCl as a function of concentration of LaCl{sub 3}. The effect of adding up to 1.40 mol % CsCl was also investigated. These properties were determined by measuring the open circuit potential of the La—La(III) redox couple in a high temperature molten salt electrochemical cell. Both the apparent potential and activity coefficient exhibited a strong dependence on concentration. A low concentration (0.69 mol %) of CsCl had no significant effect on the measured properties, while a higher concentration (1.40 mol %) of CsCl caused an increase (become more positive) in the apparent potential and activity coefficient at the higher range of LaCl{sub 3} concentrations.

Estimation of key physical properties for LaCl_3 in molten eutectic LiCl–KCl by fitting cyclic voltammetry data to a BET-based electrode reaction kinetics model

International Nuclear Information System (INIS)

Samin, Adib; Wang, Zhonghang; Lahti, Erik; Simpson, Michael; Zhang, Jinsuo

2016-01-01

Understanding the electrochemical properties of rare earth elements is important for developing efficient techniques for separating rare earth elements from actinides recovered during the electrodeposition process. In this study the cyclic voltammetry for lanthanum in molten LiClKCl eutectic was recorded at 773 K for different scan rates and different bulk concentrations. A model accounting for mass transport, kinetics and adsorption was applied to analyze the experimental data via performing a nonlinear least squares fit. The results of the simulation are compared against the results of a conventional analysis of the cyclic voltammograms and against the existing literature. At the scan rates used, the reduction/oxidation process is quasi-reversible. The values of diffusivities derived from simulation were larger than the ones derived commonly using equations for diffusion-limited processes. However, those equations were derived based on an assumption of reversibility. This simulation-based approach may provide a more accurate option for analyzing systems that do not exhibit reversibility.

Residual Salt Separation from the Metal Products Reduced in a LiCl-Li{sub 2}O Molten Salt

Energy Technology Data Exchange (ETDEWEB)

Hur, Jin Mok; Hong, Sun Seok; Kang, Dae Seung; Jeong, Meong Soo; Seo, Chung Seok

2006-02-15

The electrochemical reduction of spent nuclear fuel in a LiCl-Li{sub 2}O molten salt for the conditioning of spent nuclear fuel requires the separation of the residual salts from a reduced metal product after the reduction process. Considering the behavior of spent nuclear fuel during the electrochemical reduction process, a surrogate material matrix was constructed and inactive tests on a salt separation were carried out to produce the data required for the active tests. Fresh uranium metal prepared from the electrochemical reduction of U{sub 3}O{sub 8} powder was used as the surrogates of the spent nuclear fuel components which might be metallized by the electrochemical reduction process. LiCl, Li{sub 2}O, Y{sub 2}O{sub 3} and SrCl{sub 2} were selected as the components of the residual salts. Interactions between the salts and their influence on the separation of the residual salts were analyzed by differential scanning calorimetry (DSC) and thermogravimetry (TG). Eutectic melting of LiCl-Li{sub 2}O and LiCl-SrCl{sub 2} led to a melting point which was lower than that of a LiCl molten salt was observed. Residual salts were separated by a vaporization method. Co-vaporization of LiCl-Li{sub 2}O and LiCl-SrCl{sub 2} was achieved below temperatures which could make the uranium metal oxidation by Li{sub 2}O possible. The salt vaporization rates at 950 .deg. C were measured as follows: LiCl-8 wt% Li{sub 2}O > LiCl > LiCl-8 wt% SrCl{sub 2} > SrCl{sub 2}.

Effects of lithium and valproic acid on gene expression and phenotypic markers in an NT2 neurosphere model of neural development.

Directory of Open Access Journals (Sweden)

Eric J Hill

Full Text Available Mood stabilising drugs such as lithium (LiCl and valproic acid (VPA are the first line agents for treating conditions such as Bipolar disorder and Epilepsy. However, these drugs have potential developmental effects that are not fully understood. This study explores the use of a simple human neurosphere-based in vitro model to characterise the pharmacological and toxicological effects of LiCl and VPA using gene expression changes linked to phenotypic alterations in cells. Treatment with VPA and LiCl resulted in the differential expression of 331 and 164 genes respectively. In the subset of VPA targeted genes, 114 were downregulated whilst 217 genes were upregulated. In the subset of LiCl targeted genes, 73 were downregulated and 91 were upregulated. Gene ontology (GO term enrichment analysis was used to highlight the most relevant GO terms associated with a given gene list following toxin exposure. In addition, in order to phenotypically anchor the gene expression data, changes in the heterogeneity of cell subtype populations and cell cycle phase were monitored using flow cytometry. Whilst LiCl exposure did not significantly alter the proportion of cells expressing markers for stem cells/undifferentiated cells (Oct4, SSEA4, neurons (Neurofilament M, astrocytes (GFAP or cell cycle phase, the drug caused a 1.4-fold increase in total cell number. In contrast, exposure to VPA resulted in significant upregulation of Oct4, SSEA, Neurofilament M and GFAP with significant decreases in both G2/M phase cells and cell number. This neurosphere model might provide the basis of a human-based cellular approach for the regulatory exploration of developmental impact of potential toxic chemicals.

Evidence against the involvement of ionically bound cell wall proteins in pea epicotyl growth

Science.gov (United States)

Melan, M. A.; Cosgrove, D. J.

1988-01-01

Ionically bound cell wall proteins were extracted from 7 day old etiolated pea (Pisum sativum L. cv Alaska) epicotyls with 3 molar LiCl. Polyclonal antiserum was raised in rabbits against the cell wall proteins. Growth assays showed that treatment of growing region segments (5-7 millimeters) of peas with either dialyzed serum, serum globulin fraction, affinity purified immunoglobulin, or papain-cleaved antibody fragments had no effect on growth. Immunofluorescence microscopy confirmed antibody binding to cell walls and penetration of the antibodies into the tissues. Western blot analysis, immunoassay results, and affinity chromatography utilizing Sepharose-bound antibodies confirmed recognition of the protein preparation by the antibodies. Experiments employing in vitro extension as a screening measure indicated no effect upon extension by antibodies, by 50 millimolar LiCl perfusion of the apoplast or by 3 molar LiCl extraction. Addition of cell wall protein to protease pretreated segments did not restore extension nor did addition of cell wall protein to untreated segments increase extension. It is concluded that, although evidence suggests that protein is responsible for the process of extension, the class(es) of proteins which are extracted from pea cell walls with 3 molar LiCl are probably not involved in this process.

Electrochemical characterisation of CaCl2 deficient LiCl-KCl-CaCl2 eutectic melt and electro-deoxidation of solid UO2

Science.gov (United States)

Sri Maha Vishnu, D.; Sanil, N.; Mohandas, K. S.; Nagarajan, K.

2016-03-01

The CaCl2 deficient ternary eutectic melt LiCl-KCl-CaCl2 (50.5: 44.2: 5.3 mol %) was electrochemically characterised by cyclic voltammetry and polarization techniques in the context of its probable use as the electrolyte in the electrochemical reduction of solid UO2 to uranium metal. Tungsten (cathodic polarization) and graphite (anodic polarization) working electrodes were used in these studies carried out in the temperature range 623 K-923 K. The cathodic limit of the melt was observed to be set by the deposition of Ca2+ ions followed by Li+ ions on the tungsten electrode and the anodic limit by oxidation of chloride ions on the graphite electrode (chlorine evolution). The difference between the onset potential of deposition of Ca2+ and Li+ was found to be 0.241 V at a scan rate of 20 mV/s at 623 K and the difference decreased with increase in temperature and vanished at 923 K. Polarization measurements with stainless steel (SS) cathode and graphite anode at 673 K showed the possibility of low-energy reactions occurring on the UO2 electrode in the melt. UO2 pellets were cathodically polarized at 3.9 V for 25 h to test the feasibility of electro-reduction to uranium in the melt. The surface of the pellets was found reduced to U metal.

K-Cl Cotransporter 2–mediated Cl− Extrusion Determines Developmental Stage–dependent Impact of Propofol Anesthesia on Dendritic Spines

KAUST Repository

Puskarjov, Martin; Fiumelli, Hubert; Briner, Adrian; Bodogan, Timea; Demeter, Kornel; Lacoh, Claudia Marvine; Mavrovic, Martina; Blaesse, Peter; Kaila, Kai; Vutskits, Laszlo

2017-01-01

Background: General anesthetics potentiating γ-aminobutyric acid (GABA)-mediated signaling are known to induce a persistent decrement in excitatory synapse number in the cerebral cortex when applied during early postnatal development, while an opposite action is produced at later stages. Here, the authors test the hypothesis that the effect of general anesthetics on synaptogenesis depends upon the efficacy of GABA receptor type A (GABA A)-mediated inhibition controlled by the developmental up-regulation of the potassium-chloride (K-Cl) cotransporter 2 (KCC2). Methods: In utero electroporation of KCC2 was used to prematurely increase the efficacy of (GABA A)-mediated inhibition in layer 2/3 pyramidal neurons in the immature rat somatosensory cortex. Parallel experiments with expression of the inward-rectifier potassium channel Kir2.1 were done to reduce intrinsic neuronal excitability. The effects of these genetic manipulations (n = 3 to 4 animals per experimental group) were evaluated using iontophoretic injection of Lucifer Yellow (n = 8 to 12 cells per animal). The total number of spines analyzed per group ranged between 907 and 3,371. Results: The authors found a robust effect of the developmental up-regulation of KCC2-mediated Cl - transport on the age-dependent action of propofol on dendritic spines. Premature expression of KCC2, unlike expression of a transport-inactive KCC2 variant, prevented a propofol-induced decrease in spine density. In line with a reduction in neuronal excitability, the above result was qualitatively replicated by overexpression of Kir2.1. Conclusions: The KCC2-dependent developmental increase in the efficacy of GABA A -mediated inhibition is a major determinant of the age-dependent actions of propofol on dendritic spinogenesis.

K-Cl Cotransporter 2–mediated Cl− Extrusion Determines Developmental Stage–dependent Impact of Propofol Anesthesia on Dendritic Spines

KAUST Repository

Puskarjov, Martin

2017-03-16

Background: General anesthetics potentiating γ-aminobutyric acid (GABA)-mediated signaling are known to induce a persistent decrement in excitatory synapse number in the cerebral cortex when applied during early postnatal development, while an opposite action is produced at later stages. Here, the authors test the hypothesis that the effect of general anesthetics on synaptogenesis depends upon the efficacy of GABA receptor type A (GABA A)-mediated inhibition controlled by the developmental up-regulation of the potassium-chloride (K-Cl) cotransporter 2 (KCC2). Methods: In utero electroporation of KCC2 was used to prematurely increase the efficacy of (GABA A)-mediated inhibition in layer 2/3 pyramidal neurons in the immature rat somatosensory cortex. Parallel experiments with expression of the inward-rectifier potassium channel Kir2.1 were done to reduce intrinsic neuronal excitability. The effects of these genetic manipulations (n = 3 to 4 animals per experimental group) were evaluated using iontophoretic injection of Lucifer Yellow (n = 8 to 12 cells per animal). The total number of spines analyzed per group ranged between 907 and 3,371. Results: The authors found a robust effect of the developmental up-regulation of KCC2-mediated Cl - transport on the age-dependent action of propofol on dendritic spines. Premature expression of KCC2, unlike expression of a transport-inactive KCC2 variant, prevented a propofol-induced decrease in spine density. In line with a reduction in neuronal excitability, the above result was qualitatively replicated by overexpression of Kir2.1. Conclusions: The KCC2-dependent developmental increase in the efficacy of GABA A -mediated inhibition is a major determinant of the age-dependent actions of propofol on dendritic spinogenesis.

Anti-diabetic and antihypertensive activities of two flaxseed protein hydrolysate fractions revealed following their simultaneous separation by electrodialysis with ultrafiltration membranes.

Science.gov (United States)

Doyen, Alain; Udenigwe, Chibuike C; Mitchell, Patricia L; Marette, André; Aluko, Rotimi E; Bazinet, Laurent

2014-02-15

Flaxseed protein hydrolysate has been fractionated by electrodialysis with two ultrafiltration membranes (20 and 50 kDa) stacked in the system for the recovery of two specific cationic peptide fractions (KCl-F1 and KCl-F2). After 360 min of treatment, peptide migration increased as a function of time in KCl compartments. Moreover, the use of two different ultrafiltration membrane allowed concentration of the 300-400 and 400-500 Da molecular weight range peptides in the KCl-F1 and KCl-F2 fractions, respectively, compared to the initial hydrolysate. After mass spectrometry analysis, higher amounts of low molecular weight peptides were recovered in the KCl-F2 compartment while relatively higher molecular weight peptides were more detected in the KCl-F1 compartment. Amino acid analysis showed that His, Lys and Arg were especially concentrated in the KCl compartments. Finally, glucose-transport assay demonstrated that the KCl-F2 fraction increased glucose uptake while oral administration of KCl-F1 and final FPH decreased systolic blood pressure. Copyright © 2013 Elsevier Ltd. All rights reserved.

Studies of the effects of TiCl{sub 3} in LiBH{sub 4}/CaH{sub 2}/TiCl{sub 3} reversible hydrogen storage system

Energy Technology Data Exchange (ETDEWEB)

Liu Dongan [Ford Motor Company, Research and Advanced Engineering, MD 1170/RIC, Dearborn, MI 48121 (United States); Department of Mechanical Engineering, University of Michigan, 1023 H. H. Dow Building 2350 Hayward Street, Ann Arbor, MI 48109-2125 (United States); Yang Jun, E-mail: jyang27@ford.com [Ford Motor Company, Research and Advanced Engineering, MD 1170/RIC, Dearborn, MI 48121 (United States); Ni Jun [Department of Mechanical Engineering, University of Michigan, 1023 H. H. Dow Building 2350 Hayward Street, Ann Arbor, MI 48109-2125 (United States); Drews, Andy [Ford Motor Company, Research and Advanced Engineering, MD 1170/RIC, Dearborn, MI 48121 (United States)

2012-02-15

Highlights: Black-Right-Pointing-Pointer We systematically studied the effects of TiCl{sub 3} in LiBH{sub 4}/CaH{sub 2}/TiCl{sub 3} hydrogen storage system. Black-Right-Pointing-Pointer It is found that adding 0.25 TiCl{sub 3} produces fully reversible hydrogen absorption and desorption and a lower desorption temperature. Black-Right-Pointing-Pointer LiCl experiences four different states, i.e. 'formed-solid solution-molten solution-precipitation', in the whole desorption process of the system. Black-Right-Pointing-Pointer The incorporation of LiCl into LiBH{sub 4} forms more viscous molten LiBH{sub 4}{center_dot}LiCl, leading to fast kinetics. Black-Right-Pointing-Pointer The precipitation and re-incorporation of LiCl into LiBH{sub 4} lead to a fully reversible complex hydrogen storage system. - Abstract: In the present study, the effects of TiCl{sub 3} on desorption kinetics, absorption/desorption reversibility, and related phase transformation processes in LiBH{sub 4}/CaH{sub 2}/TiCl{sub 3} hydrogen storage system was studied systematically by varying its concentration (x = 0, 0.05, 0.15 and 0.25). The results show that LiCl forms during ball milling of 6LiBH{sub 4}/CaH{sub 2}/xTiCl{sub 3} and that as temperature increases, o-LiBH{sub 4} transforms into h-LiBH{sub 4}, into which LiCl incorporates, forming solid solution of LiBH{sub 4}{center_dot}LiCl, which melts above 280 Degree-Sign C. Molten LiBH{sub 4}{center_dot}LiCl is more viscous than molten LiBH{sub 4}, preventing the clustering of LiBH{sub 4} and the accompanied agglomeration of CaH{sub 2}, and thus preserving the nano-sized phase arrangement formed during ball milling. Above 350 Degree-Sign C, the molten solution LiBH{sub 4}{center_dot}LiCl further reacts with CaH{sub 2}, precipitating LiCl. The main hydrogen desorption reaction is between molten LiBH{sub 4}{center_dot}LiCl and CaH{sub 2} and not between molten LiBH{sub 4} and CaH{sub 2}. This alters the hydrogen reaction thermodynamics and

Estimation of key physical properties for LaCl{sub 3} in molten eutectic LiCl–KCl by fitting cyclic voltammetry data to a BET-based electrode reaction kinetics model

Energy Technology Data Exchange (ETDEWEB)

Samin, Adib [Nuclear Engineering Program, Department of Mechanical and Aerospace Engineering, The Ohio State University, 201 W 19th Avenue, Columbus, OH 43210 (United States); Wang, Zhonghang [Nuclear Engineering Program, Department of Mechanical and Aerospace Engineering, Metallurgical Engineering Department, University of Utah, Salt Lake City, UT 84112 (United States); Nuclear Engineering Program, Department of Mechanical and Aerospace Engineering, National Engineering Laboratory for Hydrometallurgical Cleaner Production Technology, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190 (China); Lahti, Erik [Nuclear Engineering Program, Department of Mechanical and Aerospace Engineering, The Ohio State University, 201 W 19th Avenue, Columbus, OH 43210 (United States); Simpson, Michael [Nuclear Engineering Program, Department of Mechanical and Aerospace Engineering, Metallurgical Engineering Department, University of Utah, Salt Lake City, UT 84112 (United States); Zhang, Jinsuo, E-mail: zhang.3558@osu.edu [Nuclear Engineering Program, Department of Mechanical and Aerospace Engineering, The Ohio State University, 201 W 19th Avenue, Columbus, OH 43210 (United States)

2016-07-15

Understanding the electrochemical properties of rare earth elements is important for developing efficient techniques for separating rare earth elements from actinides recovered during the electrodeposition process. In this study the cyclic voltammetry for lanthanum in molten LiClKCl eutectic was recorded at 773 K for different scan rates and different bulk concentrations. A model accounting for mass transport, kinetics and adsorption was applied to analyze the experimental data via performing a nonlinear least squares fit. The results of the simulation are compared against the results of a conventional analysis of the cyclic voltammograms and against the existing literature. At the scan rates used, the reduction/oxidation process is quasi-reversible. The values of diffusivities derived from simulation were larger than the ones derived commonly using equations for diffusion-limited processes. However, those equations were derived based on an assumption of reversibility. This simulation-based approach may provide a more accurate option for analyzing systems that do not exhibit reversibility.

Salidroside Protection Against Oxidative Stress Injury Through the Wnt/β-Catenin Signaling Pathway in Rats with Parkinson’s Disease

Directory of Open Access Journals (Sweden)

Dong-Mei Wu

2018-04-01

Full Text Available Background/Aims: Parkinson’s disease (PD is the second most common neurodegenerative disease after Alzheimer’s disease, and recent studies suggested that oxidative stress (OS contributes to the cascade that leads to dopamine cell degeneration in PD. In this study, we hypothesized that salidroside (SDS offers protection against OS injury in 6-hydroxydopamine (6-OHDA unilaterally lesioned rats as well as the underlying mechanism. Methods: SDS and LiCl (activators of the Wnt/β-catenin signaling pathway administration alone and in combination with 6-OHDA injection in rats was performed 3 days before modeling for 17 consecutive days to verify the regulatory mechanism by which SDS affects the Wnt/β-catenin signaling pathway as well as to evaluate the protective effect of SDS on PD in relation to OS in vivo. In addition, pheochromocytoma 12 (PC12 cells were incubated with 10 µmol/L SDS or LiCl alone or with both in combination for 1 h followed by a 24-h incubation with 100 µmol/L 6-OHDA to obtain in vitro data. Results: In vivo the administration of LiCl was found to ameliorate behavioral deficits and dopaminergic neuron loss; increase superoxide dismutase (SOA activity, glutathione peroxidase (GSH-Px levels, and glycogen synthase kinase 3β phosphorylation (GSK-3β-Ser9; reduce malondialdehyde (MDA accumulation in the striatum and the GSK-3β mRNA level; as well as elevate β-catenin and cyclinD1 mRNA and protein levels in 6-OHDA-injected rats. This SDS treatment regimen was found to strengthen the beneficial effect of LiCl on 6-OHDA-injected rats. In vitro LiCl treatment decreased the toxicity of 6-OHDA on PC12 cells and prevented apoptosis. Additionally, LiCl treatment increased SOA activity, GSH-Px levels, and GSK-3β-Ser9 phosphorylation; decreased MDA accumulation in the striatum and GSK-3β mRNA levels; as well as increased β-catenin and cyclinD1 mRNA and protein levels in 6-OHDA-treated PC12 cells. Additionally, SDS treatment increased

Enhancement of porous silicon photoluminescence property by lithium chloride treatment

Science.gov (United States)

Azaiez, Khawla; Zaghouani, Rabia Benabderrahmane; Khamlich, Saleh; Meddeb, Hosny; Dimassi, Wissem

2018-05-01

Porous silicon (PS) decorated by several nanostructured metal elements has still aroused interests as promising composites in many industrial applications. With the focus mainly on the synthesis, the aspect of stability against optical irradiation of such materials has so far not been thoroughly addressed. This work focuses primarily on the influence of lithium chloride solution (LiCl) treatment on the physical properties of PS. Variations in the structural and optoelectronic properties of PS were observed after immersion in (LiCl), as revealed by the obtained analyses. Moreover, enhanced photoluminescence (PL) property of the PS after passivation by lithium particles was clearly shown, and their presence on the surface of the microporous silicon was confirmed by FTIR spectroscopy and atomic force microscopy. An improvement of the minority carrier lifetime was also obtained, which was attributed to the decrease of the surface recombination velocity after LiCl treatment.

Partial substitution of NaCl by KCl and addition of flavor enhancers on probiotic Prato cheese: A study covering manufacturing, ripening and storage time.

Science.gov (United States)

Silva, Hugo L A; Balthazar, Celso F; Esmerino, Erick A; Neto, Roberto P C; Rocha, Ramon S; Moraes, Jeremias; Cavalcanti, Rodrigo N; Franco, Robson M; Tavares, Maria Inês B; Santos, Jânio S; Granato, Daniel; Costa, Renata G B; Freitas, Mônica Q; Silva, Márcia C; Raices, Renata S L; Senaka Ranadheera, C; Nazzaro, Filomena; Mortazavian, Amir M; Cruz, Adriano G

2018-05-15

Cheese is a suitable matrix to deliver probiotic strains but it contains a high amount of sodium. The effect of partial substitution of NaCl by KCl and the addition of flavor enhancers (l-arginine, yeast and oregano extract) on probiotic Prato cheese was investigated after 1, 30, and 60 d of refrigerated storage (immediately after manufacturing, and during ripening and storage). Microbiological (lactic acid bacteria and probiotic Lactobacillus casei 01 counts and survival under gastrointestinal conditions), physicochemical (pH, proteolysis, fatty acids), bioactivity (antioxidant effect and angiotensin I-converting enzyme inhibitory activity), rheological, and water mobility by means of time domain low-field nuclear magnetic resonance were investigated. Significant changes in probiotic survival were observed; however, the sodium reduction and the addition of flavor enhancers did not constitute an obstacle to L. casei 01 (>10 8  CFU/g) during storage. Slight changes were observed in proteolysis, bioactivity, water mobility, texture profile, and fatty acids of the cheeses as a function of the flavor enhancer added. The sodium reduction and the supplementation of Prato cheese with probiotic cultures may be an effective alternative to the production of a potentially functional cheese. Copyright © 2017 Elsevier Ltd. All rights reserved.

NKS1, Na+- and K+-sensitive 1, regulates ion homeostasis in an SOS-independent pathway in Arabidopsis

KAUST Repository

Choi, Wonkyun

2011-04-01

An Arabidopsis thaliana mutant, nks1-1, exhibiting enhanced sensitivity to NaCl was identified in a screen of a T-DNA insertion population in the genetic background of Col-0 gl1 sos3-1. Analysis of the genome sequence in the region flanking the T-DNA left border indicated two closely linked mutations in the gene encoded at locus At4g30996. A second allele, nks1-2, was obtained from the Arabidopsis Biological Resource Center. NKS1 mRNA was detected in all parts of wild-type plants but was not detected in plants of either mutant, indicating inactivation by the mutations. Both mutations in NKS1 were associated with increased sensitivity to NaCl and KCl, but not to LiCl or mannitol. NaCl sensitivity was associated with nks1 mutations in Arabidopsis lines expressing either wild type or alleles of SOS1, SOS2 or SOS3. The NaCl-sensitive phenotype of the nks1-2 mutant was complemented by expression of a full-length NKS1 allele from the CaMV35S promoter. When grown in medium containing NaCl, nks1 mutants accumulated more Na+ than wild type and K +/Na+ homeostasis was perturbed. It is proposed NKS1, a plant-specific gene encoding a 19 kDa endomembrane-localized protein of unknown function, is part of an ion homeostasis regulation pathway that is independent of the SOS pathway. © 2011 Elsevier Ltd. All rights reserved.

bHLH106 Integrates Functions of Multiple Genes through Their G-Box to Confer Salt Tolerance on Arabidopsis.

Science.gov (United States)

Ahmad, Aftab; Niwa, Yasuo; Goto, Shingo; Ogawa, Takeshi; Shimizu, Masanori; Suzuki, Akane; Kobayashi, Kyoko; Kobayashi, Hirokazu

2015-01-01

An activation-tagging methodology was applied to dedifferentiated calli of Arabidopsis to identify new genes involved in salt tolerance. This identified salt tolerant callus 8 (stc8) as a gene encoding the basic helix-loop-helix transcription factor bHLH106. bHLH106-knockout (KO) lines were more sensitive to NaCl, KCl, LiCl, ABA, and low temperatures than the wild-type. Back-transformation of the KO line rescued its phenotype, and over-expression (OX) of bHLH106 in differentiated plants exhibited tolerance to NaCl. Green fluorescent protein (GFP) fused with bHLH106 revealed that it was localized to the nucleus. Prepared bHLH106 protein was subjected to electrophoresis mobility shift assays against E-box sequences (5'-CANNTG-3'). The G-box sequence 5'-CACGTG-3' had the strongest interaction with bHLH106. bHLH106-OX lines were transcriptomically analyzed, and resultant up- and down-regulated genes selected on the criterion of presence of a G-box sequence. There were 198 genes positively regulated by bHLH106 and 36 genes negatively regulated; these genes possessed one or more G-box sequences in their promoter regions. Many of these genes are known to be involved in abiotic stress response. It is concluded that bHLH106 locates at a branching point in the abiotic stress response network by interacting directly to the G-box in genes conferring salt tolerance on plants.

NKS1, Na+- and K+-sensitive 1, regulates ion homeostasis in an SOS-independent pathway in Arabidopsis

KAUST Repository

Choi, Wonkyun; Baek, Dongwon; Oh, Dongha; Park, Jiyoung; Hong, Hyewon; Kim, Woeyeon; Bohnert, Hans Jü rgen; Bressan, Ray Anthony; Park, Hyeongcheol; Yun, Daejin

2011-01-01

An Arabidopsis thaliana mutant, nks1-1, exhibiting enhanced sensitivity to NaCl was identified in a screen of a T-DNA insertion population in the genetic background of Col-0 gl1 sos3-1. Analysis of the genome sequence in the region flanking the T-DNA left border indicated two closely linked mutations in the gene encoded at locus At4g30996. A second allele, nks1-2, was obtained from the Arabidopsis Biological Resource Center. NKS1 mRNA was detected in all parts of wild-type plants but was not detected in plants of either mutant, indicating inactivation by the mutations. Both mutations in NKS1 were associated with increased sensitivity to NaCl and KCl, but not to LiCl or mannitol. NaCl sensitivity was associated with nks1 mutations in Arabidopsis lines expressing either wild type or alleles of SOS1, SOS2 or SOS3. The NaCl-sensitive phenotype of the nks1-2 mutant was complemented by expression of a full-length NKS1 allele from the CaMV35S promoter. When grown in medium containing NaCl, nks1 mutants accumulated more Na+ than wild type and K +/Na+ homeostasis was perturbed. It is proposed NKS1, a plant-specific gene encoding a 19 kDa endomembrane-localized protein of unknown function, is part of an ion homeostasis regulation pathway that is independent of the SOS pathway. © 2011 Elsevier Ltd. All rights reserved.

The roles of anion and solvent transport during the redox switching process at a poly(butyl viologen) film studied by an EQCM

Energy Technology Data Exchange (ETDEWEB)

Hsu, Chih-Yu.; Liao, Chun-Hao [Department of Chemical Engineering, National Taiwan University, Taipei 10617 (China); Ho, Kuo-Chuan [Department of Chemical Engineering, National Taiwan University, Taipei 10617 (China); Institute of Polymer Science and Engineering, National Taiwan University, Taipei 10617 (China)

2008-02-15

In this study, three electrolytes (KCl, LiCl, and KNO{sub 3}, each at 0.5 M in aqueous solution) were chosen to study the ion and solvent effect on the redox performance of poly(butyl viologen) (PBV) thin-films between its di-cation and radical-cation state, which is referred as its first redox couple. Before considering the role of ionic transport on the redox process, the exchange between ferrocyanide and anion should be completed. Since the deposition solution of PBV contains potassium ferrocyanide, the residual ferrocyanides inside the films would be exchanged by smaller anions from the bulk solution during the redox reaction of PBV. From cyclic voltammetry (CV) and electrochemical quartz crystal microbalance (EQCM) results, the exchange was almost complete around 50 cycles when scanning the potential within its first redox range. After completion of the exchange process, the transfer would reach a steady state. At 50 cycles, the EQCM results suggested that the transport involves anions and water only for both being extracted upon reduction and being inserted upon oxidation. Therefore, we could obtain the molar fluxes of Cl{sup -}, NO{sub 3}{sup -}, and water. Besides, the average numbers of accompanying water were calculated to be about 24.8 per Cl{sup -} and 14.2 per NO{sub 3}{sup -} upon redox switching process. The instantaneous water to anion molar ratios at any potential were also obtained for Cl{sup -} and NO{sub 3}{sup -}. (author)

Solubility of some phenolic compounds in aqueous alkali metal nitrate solutions from (293.15 to 318.15) K

Energy Technology Data Exchange (ETDEWEB)

Noubigh, Adel [Laboratoire de Physico-chimie des materiaux, IPEST, BP51, 2070 La MARSA (Tunisia)], E-mail: Adel.anoubigh@ipest.rnu.tn; Cherif, Mourad [IPEIEM, Universite de Tunis-El Manar, BP244. 2096. El Manar II (Tunisia); Provost, Elise [Laboratoire Chimie et procedes, ENSTA, 32 Rue de Boulevard Victor, 75739 Paris, Cedex 15 (France); Abderrabba, Manef [Laboratoire de Physico-chimie des materiaux, IPEST, BP51, 2070 La MARSA (Tunisia)

2008-11-15

This paper is continuation of the study concerning the solubility-temperature dependence data for some phenolic compounds (PhC), contained in olive mill wastewater (OMWW), in two nitrate salts (KNO{sub 3} and NaNO{sub 3}) aqueous solutions. The solubilities of PhC were determined in the temperature ranging from (293.15 to 318.15) K. It has been observed that the solubility, in aqueous nitrate solutions, increases with increasing temperature. Results showed that alkali metal nitrate has a salting-out effect on the solubility of PhC. The effect of the anion of the electrolyte on the solubility of PhC is observed by comparing these results with values reported in the previous papers for the effect of LiCl, NaCl and KCl. For each cation, the solubilites of the phenolic compounds are higher with nitrate anion than with chloride anion. Results were interpreted in terms of the salt hydration shells and the ability of the solute to form hydrogen-bond with water. The solubility data were accurately correlated by a semi empirical equation. The standard molar Gibbs free energies of transfer of PhC ({delta}{sub tr}G{sup 0}) from pure water to aqueous solutions of the nitrate salts have been calculated from the solubility data. The decrease in solubility is correlated to the positive {delta}{sub tr}G{sup 0} value which is mainly of enthalpic origin.

An alkali ion source based on graphite intercalation compounds for ion mobility spectrometry

International Nuclear Information System (INIS)

Tabrizchi, Mahmoud; Hosseini, Zahra S

2008-01-01

A variety of alkali cation emitters were developed as the ion source for ion mobility spectrometry. The cation emitters were constructed based on alkali ion graphite intercalation compounds (GICs). The compounds were prepared by fusing alkali salts with ground graphite. In order to produce alkali ions, the compounds were loaded on a filament and heated to red. Reactant ions of the form alk + ions were observed for the alkali salts NaCl, KCl.LiCl, CsCl and SrCl. In addition to Na + ions, K + ions were observed at the beginning of thermionic emission from Na-GIC. This is due to the low ionization potential of potassium that exists in trace amounts in sodium salts. In addition to the potassium ion, Na + was observed in the case of LiCl salt. The Na + and K + peaks originating from impurities totally disappeared after about 40 min. However, the thermionic emission of the main ion of the corresponding salt lasted for several days. No negative ions were observed upon reversing the drift field. Selected organic compounds (methyl isobutyl ketone, dimethyl sulfoxide, acetone and tetrahydrofuran) were also ionized via alkali cation attachment reaction. Distinct ion mobility patterns were observed for different substances using one type of alkali reactant ion. However, the ion mobility pattern for a given substance changed when a different alkali reactant ion was used. Ammonia and amines were not ionized when this source was used

Electrochemical studies and analysis of 1–10 wt% UCl{sub 3} concentrations in molten LiCl–KCl eutectic

Energy Technology Data Exchange (ETDEWEB)

Hoover, Robert O., E-mail: roberthoover@vandals.uidaho.edu [Chemical and Materials Engineering Department and Nuclear Engineering Program, University of Idaho, Idaho Falls, Center for Advanced Energy Studies, 995 University Blvd, Idaho Falls, ID 83401 (United States); Shaltry, Michael R., E-mail: mshaltry@uidaho.edu [Chemical and Materials Engineering Department and Nuclear Engineering Program, University of Idaho, Idaho Falls, Center for Advanced Energy Studies, 995 University Blvd, Idaho Falls, ID 83401 (United States); Martin, Sean, E-mail: Sean.martin@xenuclear.com [Department of Engineering Physics, University of Wisconsin-Madison, 1415 Engineering Drive, Madison, WI 53706 (United States); Sridharan, Kumar, E-mail: kumar@engr.wisc.edu [Department of Engineering Physics, University of Wisconsin-Madison, 1415 Engineering Drive, Madison, WI 53706 (United States); Phongikaroon, Supathorn, E-mail: supathor@uidaho.edu [Chemical and Materials Engineering Department and Nuclear Engineering Program, University of Idaho, Idaho Falls, Center for Advanced Energy Studies, 995 University Blvd, Idaho Falls, ID 83401 (United States)

2014-09-15

Three electrochemical methods – cyclic voltammetry (CV), chronopotentiometry (CP), and anodic stripping voltammetry (ASV) – were applied to solutions of up to 10 wt% UCl{sub 3} in the molten LiCl–KCl eutectic salt at 500 °C to determine electrochemical properties and behaviors and to help provide a scientific basis for the development of an in situ electrochemical probe for determining the concentration of uranium in a used nuclear fuel electrorefiner. Diffusion coefficients of UCl{sub 4} and UCl{sub 3} were calculated to be (6.72 ± 0.360) × 10{sup −6} cm{sup 2}/s and (1.04 ± 0.17) × 10{sup −5} cm{sup 2}/s, respectively. Apparent standard reduction potentials were determined to be (−0.381 ± 0.013) V and (−1.502 ± 0.076) V vs. 5 mol% Ag/AgCl or (−1.448 ± 0.013) V and (−2.568 ± 0.076) V vs. Cl{sub 2}/Cl{sup −} for the U(IV)/U(III) and U(III)/U redox couples, respectively. In comparing this data with supercooled thermodynamic data to determine activity coefficients, the thermodynamic database used was important with resulting activity coefficients ranging from 2.34 × 10{sup −3} to 1.08 × 10{sup −2} for UCl{sub 4} and 4.94 × 10{sup −5} to 4.50 × 10{sup −4} for UCl{sub 3}. Of anodic stripping voltammetry and cyclic voltammetry anodic or cathodic peaks, the CV cathodic peak height divided by square root of scan rate was shown to be the most reliable method of determining UCl{sub 3} concentration in the molten salt.

A study of integrated cathode assembly for electrolytic reduction of uranium oxide in LiCl-Li2O molten salt

International Nuclear Information System (INIS)

Park, Sung Bin; Seo, Jung Seok; Kang, Dae Seung; Kwon, Sun Kil; Park, Seong Won

2004-01-01

Interest of electrolytic reduction of uranium oxide is increasing in treatment of spent metal fuels. Argonne National Laboratory (ANL) has reported the experimental results of electrochemical reduction of uranium oxide fuel in bench-scale apparatus with cyclic voltammetry, and has designed high-capacity reduction (HCR) cells and conducted three kg-scale UO 2 reduction runs. From the cyclic voltammograms, the mechanism of electrolytic reduction of metal oxides is analyzed. The uranium oxide in LiCl-Li 2 O is converted to uranium metal according to the two mechanism; direct and indirect electrolytic reduction. In this study, cyclic voltammograms for LiCl-3wt% Li 2 O system and U 3 O 8 -LiCl-3wt% Li 2 O system using the 325-mesh stainless steel screen in cathode assembly have been obtained. Direct electrolytic reduction of uranium oxide in LiCl-3wt% Li 2 O molten salt has been conducted

Modulación Contextual en la Extinción: Recuperación de una Aversión Condicionada al Sabor en un Tercer Contexto

Directory of Open Access Journals (Sweden)

Rodolfo Bernal-Gamboa

2011-01-01

Full Text Available Este experimento se diseñó para evaluar la renovación ABC con un procedimiento de condicionamiento de aversión al sabor (CAS en tres fases: adquisición, extinción y prueba. Durante la adquisición, 15 ratas Wistar, asignadas a los grupos ABC y ABB, tuvieron acceso a una solución con sacarosa y posteriormente recibieron una inyección de cloruro de litio (LiCl en el Contexto A. En la extinción, ambos grupos bebieron la solución con sacarosa sin la administración del LiCl en el Contexto B. En la prueba, los grupos tuvieron acceso a la solución con sacarosa sin administrarles LiCl en el contexto de extinción para el grupo ABB, y en un tercer contexto para el grupo ABC. Los resultados mostraron la recuperación de la aversión condicionada al sabor únicamente en el grupo ABC.

Fabrication of Ordered Nanopattern by using ABC Triblock Copolymer with Salt in Toluene

OpenAIRE

Huang, Hailiang; Zhong, Benbin; Zu, Xihong; Luo, Hongsheng; Lin, Wenjing; Zhang, Minghai; Zhong, Yazhou; Yi, Guobin

2017-01-01

Ordered nanopatterns of triblock copolymer polystyrene-block-poly(2-vinylpyridine)-block- poly (ethylene oxide)(PS-b-P2VP-b-PEO) have been achieved by the addition of lithium chloride (LiCl). The morphological and structural evolution of PS-b-P2VP-b-PEO/LiCl thin films were systematically investigated by varying different experimental parameters, including the treatment for polymer solution after the addition of LiCl, the time scale of ultrasonic treatment and the molar ratio of Li+ ions to t...

Characterization of incomplete fusion in the reactions Ar + KCl at 32,40,52 and 74 MeV/u

International Nuclear Information System (INIS)

Bisquer, E.

1996-01-01

Heavy ion collisions at intermediate energies (10 to 100 A.MeV) have been investigated and gave evidence to the persistence of so-called low energy mechanisms such as incomplete fusion. This thesis aims at determining the energy threshold beyond which such a mechanism does not occur any more. First we investigated the so-called conventional incomplete fusion. This mechanism is well known from low energy studies: a thermalized compound nucleus is formed which further de-excites by evaporating particles. Residues will be therefore detected in coincidence with mainly light particles. Ar + KCl at incident energies of 32, 40, 52 and 74 A.MeV has been selected for this analysis. These experiments have been performed using the INDRA multidetector in GANIL (Caen). The detection performance of INDRA allowed to use new analysis methods via global variables. In a first step, global variables have been compared in order to find the one that is the most appropriate to our study. Then incomplete fusion events have been extracted from raw events recorded at incident energies of 32, 40 and 52 A.MeV. It turned out that the contribution of this mechanisms was very weak at 52. A.MeV. It turned out that the contribution of this mechanism was very weak at 52 A.MeV and even zero at 74 A.MeV. We then investigated events in which three fragments were detected which could possibly sign multifragmentation. We did not find instantaneous multifragmentation with any expansion contribution. We also performed BNV simulations in order to compare our experimental results to model predictions, solving in a semi-classical way the Vlasov transport equation. A good agreement has been obtained on the size of the compound nucleus formed. However the excitation energy has not been reproduced, as the code seems to overestimate the energy taken away by preequilibrium particles. Incomplete fusion decreases as a function of energy but is not replaced by instantaneous multifragmentation with any expansion

Lab-Scale Electrodeposition Behaviors of Pr(III) with Use of Quartz Cell in Molten LiCl-KCl Eutectic

Energy Technology Data Exchange (ETDEWEB)

Jee, Young Taek; Yun, Jong-Il [KAIST, Daejeon (Korea, Republic of)

2016-10-15

As electrorefining is proceeded, all actinides and lanthanides in metallic form are electrochemically oxidized and dissolved into the salt, while UCl{sub 3} in the salt is reduced and forms U-metal at solid cathodes. Since this unit process includes diverse actinides and recovers most of uranium, information on stream of nuclear materials and electrochemical condition inside of electrorefiner must continuously be notified not only for its performance assessment and process prediction but also for its safeguards. Currently, there are several computational models for electrorefiner (REFIN, ERAD, and etc.). However, the absence of model which reflects the change in surface area of cathode due to electrodeposition of UCl{sub 3} critically disturbs the precision of simulation. The change in surface area leads the change in current density, diffusion layer, potential and current gradient, and thus changes the entire electrochemical conditions in electrorefiner. In this paper, as a beginning step of investigating electrodeposition behavior of lanthanides and actinides, lab-scale electrodeposition experiments and methodological evaluation on the use of quartz cell are performed. In the lab-scale electrodeposition, sizes of quartz cell and deposited material became crucial factors for precise analysis of experiments. In a typical stabilized electrodeposition, CA diagram showed large plateau with reasonably increased magnitude of current due to the increase in surface area of working electrode. The amount of charge transferred (-61.55 C) can be utilized for concentration balance. According to ICP-OES, the decreased amount of bulk was 0.301 wt. % which was close to the expected decrease from the information of charge flow (0.29 wt. %). However, deposited material in contact with quartz wall in molten LiCl-KCl eutectic led a spontaneous reaction between each other. As an indicator of this undesired reaction, the cell became black, and enormous amount of charge was consumed. In

Stabilization/Solidification of Radioactive LiCl-KCl Waste Salt by Using SiO{sub 2}-Al{sub 2}O{sub 3}-P{sub 2}O{sub 5}(SAP) Inorganic Composite: Part 2. The Effect of SAP Composition on Stabilization/Solidification

Energy Technology Data Exchange (ETDEWEB)

Ahn, Soo Na; Park, Hwan Seo; Cho, In Hak; Kim, In Tae; Cho, Yong Zun [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2012-03-15

Metal chloride waste is generated as a main waste streams in a series of electrolytic processes of a pyrochemical process. Different from carbonate or nitrate salt, metal chloride is not decomposed into oxide and chlorine but it is just vaporized. Also, it has low compatibility with conventional silicate glasses. Our research group adapted the dechlorination approach for the immobilization of waste salt. In this study, the composition of SAP (SiO{sub 2}-Al{sub 2}O{sub 3}-P{sub 2}O{sub 5}) was adjusted to enhance the reactivity and to simplify the solidification process as a subsequent research. The addition of Fe{sub 2}O{sub 3} into the basic SAP decreased the SAP/Salt ratio in weight from 3 for SAP 1071 to 2.25 for M-SAP(Fe=0.1). The experimental results indicated that the addition of Fe{sub 2}O{sub 3} increased the reactivity of M-SAP with LiCl-KCl but the reactivity gradually decreased above Fe=0.1. Also, introducing B{sub 2}O{sub 3} into M-SAP requires no glass binder for the consolidation of reaction products. U-SAP (SiO{sub 2}-Al{sub 2}O{sub 3}-P{sub 2}O{sub 5}) could effectively dechlorinate the LiCl-KCl waste and its reaction product could be consolidated as a monolithic form without a glass binder. The leaching test result indicated that U-SAP 1071 was more durable than other SAPs wasteform. By using U-SAP, 1 g of waste salt could generated 3 - 4 g of wasteform for final disposal. The final volume would be about 3 - 4 times lower than the glass-bonded sodalite. From these results, it could be concluded that the dechlorination approach using U-SAP would be one of prospective methods to manage the volatile waste salt.

Dehydration and hydration behavior of metal-salt-modified materials for chemical heat pumps

International Nuclear Information System (INIS)

Ishitobi, Hirokazu; Uruma, Keirei; Takeuchi, Masato; Ryu, Junichi; Kato, Yukitaka

2013-01-01

Lithium chloride (LiCl) modified magnesium hydroxide (Mg(OH) 2 ) is a potential new material for chemical heat pumps. However, there is insufficient information concerning its dehydration and hydration behavior. In this study, the dehydration and hydration reactions, corresponding to the heat storage and the heat output operations, respectively, of authentic Mg(OH) 2 and LiCl-modified Mg(OH) 2 were investigated by thermogravimetric methods and near infrared spectroscopy. The dehydration of authentic Mg(OH) 2 proceeded as a one-step reaction. In contrast, the dehydration of LiCl-modified Mg(OH) 2 occurred in two steps. The dehydration reaction rates were increased by LiCl modification of the Mg(OH) 2 surface, while the activation energy for the first-order dehydration reaction was lowered. The mechanism for the hydration reaction of magnesium oxide (MgO) was different to that for the hydration of LiCl-modified MgO. This difference was explained by the effect of the LiCl on the MgO particle surface. - Highlights: ► LiCl-modified Mg(OH) 2 is a candidate material for chemical heat pumps. ► The dehydration reaction of LiCl-modified Mg(OH) 2 is a two-step reaction. ► The dehydration reaction of Mg(OH) 2 was enhanced by LiCl modification. ► The hydration mechanisms of authentic MgO and LiCl-modified MgO were different.

The Aversive Agent Lithium Chloride Suppresses Phasic Dopamine Release Through Central GLP-1 Receptors.

Science.gov (United States)

Fortin, Samantha M; Chartoff, Elena H; Roitman, Mitchell F

2016-02-01

Unconditioned rewarding stimuli evoke phasic increases in dopamine concentration in the nucleus accumbens (NAc) while discrete aversive stimuli elicit pauses in dopamine neuron firing and reductions in NAc dopamine concentration. The unconditioned effects of more prolonged aversive states on dopamine release dynamics are not well understood and are investigated here using the malaise-inducing agent lithium chloride (LiCl). We used fast-scan cyclic voltammetry to measure phasic increases in NAc dopamine resulting from electrical stimulation of dopamine cell bodies in the ventral tegmental area (VTA). Systemic LiCl injection reduced electrically evoked dopamine release in the NAc of both anesthetized and awake rats. As some behavioral effects of LiCl appear to be mediated through glucagon-like peptide-1 receptor (GLP-1R) activation, we hypothesized that the suppression of phasic dopamine by LiCl is GLP-1R dependent. Indeed, peripheral pretreatment with the GLP-1R antagonist exendin-9 (Ex-9) potently attenuated the LiCl-induced suppression of dopamine. Pretreatment with Ex-9 did not, however, affect the suppression of phasic dopamine release by the kappa-opioid receptor agonist, salvinorin A, supporting a selective effect of GLP-1R stimulation in LiCl-induced dopamine suppression. By delivering Ex-9 to either the lateral or fourth ventricle, we highlight a population of central GLP-1 receptors rostral to the hindbrain that are involved in the LiCl-mediated suppression of NAc dopamine release.

Drugs and taste aversion

International Nuclear Information System (INIS)

Rondeau, D.B.; Jolicoeur, F.B.; Merkel, A.D.; Wayner, M.J.

1981-01-01

The literature on the effects of drugs on the acquisition and the magnitude of taste aversion is reviewed and discussed. Then, the results of a series of experiments on the effects of phenobarbital and related drugs on taste aversion are reported. A standard taste aversion model was used in all experiments; test drugs were injected prior to drinking in a one bottle situation on the first test day following the taste aversion treatment. Phenobarbital in doses ranging from 20 to 80 mg/kg significantly attenuated taste aversion induced by lithium chloride (LiCl) and x-radiation, the maximal effect occurred with the 60 mg/kg dose. The attenuating effect was found to be dependent upon the magnitude of the aversion to the sapid solution. Phenobarbital completely abolished aversion produced by 0.375 mEq LiCl while the attenuation effect decreased linearly with higher doses of LiCl. Results also indicate that phenobarbital's attenuating effect cannot be solely attributed to its dipsogenic characteristic or to its state dependent learning effect. Attenuation of LiCl aversion to a saccharin solution was also observed following single doses of amobarbital, 30 mg/kg, pentobarbital, 15 mg/kg, and chloropromazine, 0.75 mg/kg. Taste aversion was not affected by other doses of those drugs or by hexobarbital, barbital, and chlordiazepoxide. Phenobarbital's attenuating effect on taste aversion is discussed in relation to other known behavioral and neurophysiological effects of the drug

Profile counting; Comptage suivant l'axe principal du corps; Issledovanie schetchikom vdol' vsego tela; Recuento segun el eje principal del cuerpo

Energy Technology Data Exchange (ETDEWEB)

Pochin, E E [Medical Research Council, Department of Clinical Research, University College Hospital Medical School, University Street, London, W. C. 1 (United Kingdom)

1959-07-01

izmereniyakh, a issledovanie schetchikom prodolzhaetsya s tsel'yu sledit' za peremeshniem ili izmeneniem kontsentratsii v ehtikh organakh. EHtot metod byl ispol'zovan pri izuchenii kontsentratsii I{sup 131} i obmena veshchestv v rakovykh opukholyakh shchitovidnoj zhelezy, i predstoit obsudit' ego tsennost' dlya lecheniya takikh opukholej radioaktivny m iodom. On primenyalsya takzhe dlya izucheniya raspredeleniya mechenogo tiroksina i tijodotronina posle ikh vvedeniya v venu i chastits okisi ittriya{sup 90} posle vnutrilegochnoj arterial'noj infektsii, a takzhe drugikh izotopov s pomoshch'yu gamma i tormoznogo izlucheniya. EHtot metod uproshchaet, v udobnykh v klinicheskom otnoshenii usloviyakh, sostavlenie skhemy vsego tela, kotoraya, v chastnosti, pozvolyaet provesti kolichestvennoe sravnenie raspredeleniya izotopov v razlichnye promezhutki vremeni posle vvedeniya odnoj ili neskol'kikh posleduyushchikh doz radioizotopa. (author)

Analysis of electron pair production in the collision system Ar+KCl at 1.76 AGeV

International Nuclear Information System (INIS)

Lang, Simon Martin

2008-01-01

The HADES-spectrometer at GSI is used to measure the production of the light vector mesons ρ, ω and φ at SIS energies. Therefore, the medium sized collision system Ar+KCl was measured at 1.76 AGeV kinetic energy of beam particles. In this system the density of particle tracks is much larger as compared to the formerly used collision system C+C, making it necessary to upgrade the data analysis. The previous method of hard-cuts - used for particle identification - was replaced by a newly developed multi-variate analysis based on an artificial neural network. This algorithm has the benefit, that it is more robust against fluctuations in one or more of the used detector observables. This increases the overall efficiency and purity of the analysis procedure. Furthermore, the reconstruction of particle tracks inside the HADES spectrometer is based on a few position information, only. During analysis of raw data, these information are combined to a artificially large manifold of tracks. This leads to the general problem that one has to select the maximum number of true physical tracks out of this set of tracks per event. A new method of track selection is used to filter the data not only to select single tracks, but also to identify electron pairs created during Dalitz-decay of π 0 mesons, which build the bulk of combinatorial background. The result of the analysis is an efficiency corrected invariant mass spectrum of electron pairs, normalized to the mean number of pions per event. The spectrum consists of more than 16,000 pairs with an invariant mass larger than 150 MeV. In total more than 150000 pairs were found. A first comparison with the spectra calculated by using the old analysis approach shows a 30% enhancement in yield of reconstructed electron pairs. A first comparison with a simple thermal model implemented by the Pluto event generator, opens the possibility to compare the measured pair yield of ω and φ mesons via m T -scaling with the yield of η mesons

Enhancing the rheological properties and shale inhibition behavior of water-based mud using nanosilica, multi-walled carbon nanotube, and graphene nanoplatelet

Directory of Open Access Journals (Sweden)

A. Aftab

2017-06-01

Full Text Available Five different drilling mud systems namely potassium chloride (KCl as a basic mud, KCl/partial hydrolytic polyacrylamide (PHPA, KCl/graphene nanoplatelet (GNP, KCl/nanosilica and KCl/multi-walled carbon nano tube (MWCNT were prepared and investigated for enhancement of rheological properties and shale inhibition. Nanoparticles were characterized in drilling mud using transmission electron microscope (TEM analysis. Mineralogical analysis of shale was examined by X-ray diffraction (XRD. Five shale plugs were prepared using compactor cell for the determination of shale swelling. Shale swelling was determined using the linear swell meter (LSM for 20 hours. Results revealed that basic mud and KCl/polymer mud systems shows 30% and 24% change in shale volume. MWCNT, nanosilica and GNP were added separately in the KCl mud system. 0.1 ppb of each MWCNT and nanosilica showed 32% and 33% change in shale volume. However, when the shale was interacted with WBM containing 0.1 ppb of GNP, it was found that only 10% change in shale volume occurred. The results showed that the addition of nanoparticles in the KCl mud system improved the shale inhibition. API, HPHT filtrate loss volume, plastic viscosity (PV and yield point (YP were improved using GNP. It is learned from the experimental work that small concentration of KCl with GNP can mitigate shale swelling compared to the mud contains higher concentration of KCl and PHPA in WBM. Thus, GNP can be a better choice for enhancement of WBM performance.

Experimental testing of a small sorption air cooler using composite material made from natural siliceous shale and chloride

International Nuclear Information System (INIS)

Liu, Hongzhi; Nagano, Katsunori; Morita, Atsushi; Togawa, Junya; Nakamura, Makoto

2015-01-01

A sorption air cooler experimental setup including a reactor and fin tube condenser/evaporator was built. The reactor was developed with inner copper fins and dual layers of curing copper meshes. Composite material made by impregnating LiCl into the mesopores of Wakkanai Siliceous Shale (WSS) micropowders was packed between the intervals of two fins. Heat transfer was enhanced by the attached fins, and the dual layers of curing meshes installed between each interval of two fins were designed to improve the sorbate mass transfer. On the other hand, the fin-tube evaporator/condenser with fins outside is valuable for improving the convective heat transfer between the functional water inside the evaporator/condenser and the flowing outside heat transfer medium, air. The sorption capacity of the composite material increased dramatically after being impregnated with LiCl. Among the four tested samples, WSS + 40 wt% LiCl exhibits the best performance. A regeneration temperature of 80 °C appears to be optimal for obtaining both a high COP and high specific cooling power. A lower condensation temperature can increase the cooling power. The sorption and desorption times of 60 min yield a reasonable compromise between cooling COP and mass specific cooling powers. The developed sorption air cooler system using WSS + 40 wt% LiCl can store heat at temperatures below 100 °C and produce cooling energy with a cooling coefficient of performance (COP) of approximately 0.3. - Highlights: • Mesoporous composite material was developed using natural siliceous shale and LiCl. • Properties of the developed material were measured. • A sorption air cooler experimental setup including an inner-fin reactor and a fin tube condenser/evaporator was built. • The performance of the composite material in the sorption air cooler was examined. • The sorption air cooler system can produce cooling energy with a cooling COP around 0.3

Synthesis of CaCrO{sub 4} powders for the cathode material of the thermal battery by GNP and electrochemical characteristics of Ca/LiCl-KCl/CaCrO{sub 4} thermal battery system

Energy Technology Data Exchange (ETDEWEB)

Kim, Whung Whoe

2000-04-01

Thermal batteries are one of the devices employing solid electrolyte that are not nonconductive at ambient temperature, and activated by electrochemical reaction when the sufficient heat is supplied to electrolyte to melt. The demand of thermal batteries would be increased because it is cost effective and highly reliable in that no maintenance is necessary, electric power can be generated as necessary and no self discharge unlike the other primary batteries. These thermal batteries are used to the military purposes and satellite communication systems and as an emergency power sources, applied to the important places where power supply should not be interrupted, such as hospital, powder plants, ships and portable communication devices. Therefore, the purpose of this study was focused to obtain the manufacturing technologies of thermal battery on our own, after manufacturing the CaCrO{sub 4} produced by GNP and investigating the electrochemical characteristics of Ca/LiCl-KCl+CaCrO{sub 4}/Ni.

Effect of wood ash and K-fertilization on {sup 137}Cs uptake by selected forest plants

Energy Technology Data Exchange (ETDEWEB)

Mandro, Yrii N. [Zhytomyr State Technological University, P.O. Box 10005 Zhytomyr (Ukraine); Rosen, Klas [Swedish University of Agricultural Sciences P.O. Box 7070 SE-750 07 Uppsala (Sweden); Vinichuk, Mykhailo M. [Zhytomyr State Technological University, P.O. Box 10005 Zhytomyr (Ukraine); Swedish University of Agricultural Sciences P.O. Box 7070 SE-750 07 Uppsala (Sweden)

2014-07-01

Accumulation {sup 137}Cs by different forest plants and trees after fertilization of soil with potassium and wood ash ({sup 137}Cs-contaminated and non-contaminated) in forest ecosystems of Ukraine contaminated by radionuclides after Chernobyl accident in 1986 was studied. Experiment is performed in Bazar forestry, Zhytomyr region, Ukraine, located about 70 km (51 deg. 5'35'' N, 29 deg. 18'56'' E) from Chernobyl NPP. Potassium fertilizer (KCl, wooden ash (Ash), and {sup 137}Cs-contaminated ash ({sup 137}CsAsh) in different combinations) were spread on the forest floor in April 2012 at a rate corresponding 100 kg/ha potassium. The experiment layout was as follows: 1- Control (no fertilizers were applied), 2- KCl, 3- Ash + KCl, 4- Ash + {sup 137}CsAsh, 5- Ash, 6- {sup 137}CsAsh + KCl. Samples (leaves and annual shoots) of blueberry (Vaccinium myrtillus), cowberry (Vaccinium vitis-idaea), rowan (Sorbus aucuparia), birch (Betula), buckthorn (Frangula) and oak (Quercus robur) and also mushrooms (fruit bodies of Russula, Lactarius, Cantharellus, Collybia etc.) and berries (blueberry and cowberry) were taken monthly from each treatment. Samples were measured for {sup 137}Cs with calibrated HPGe detectors. The results of the first year studies show variation of Transfer Factors (TF) for different plants and for the same plants on different treatments. The effect of fertilization was found for blueberry on Ash-applicated (TF = 0.0085 ± 0.0025), {sup 137}CsAsh + KCl-applicated (TF = 0.0105 ± 0.0060) and Ash + KCl-applicated (TF = 0.0123 ± 0.0058) treatments compared to Control (TF = 0.0163 ± 0.0092). Also good effect for rowan on Ash + KCl-applicated treatment (TF = 0.0067 ± 0.0024) compared to Control (TF = 0.0100 ± 0.0064). Effect was less obvious for birch on Ash + KCl-applicated treatment and for cowberry on Ash + KCl-applicated treatment. There was not found an obvious effect of fertilization for buckthorn. Positive effect of

Optimisation of potassium chloride nutrition for proper growth, physiological development and bioactive component production in Prunella vulgaris L.

Directory of Open Access Journals (Sweden)

Yuhang Chen

Full Text Available Prunella vulgaris L. is an important medicinal plant with a variety of pharmacological activities, but limited information is available about its response to potassium chloride (KCl supplementation. P. vulgaris seedlings were cultured in media with four different KCl levels (0, 1.00, 6.00 and 40.00 mM. Characteristics relating to the growth, foliar potassium, water and chlorophyll content, photosynthesis, transpiration, nitrogen metabolism, bioactive constituent concentrations and yield were determined after three months. The appropriate KCl concentration was 6.00 mM to result in the highest values for dry weight, shoot height, spica and root weight, spica length and number in P. vulgaris. The optimum KCl concentration resulted in a maximum net photosynthetic rate (Pn that could be associated with the highest chlorophyll content and fully open stomata conductance. A supply of surplus KCl resulted in a higher concentration of foliar potassium and negatively correlated with the biomass. Plants that were treated with the appropriate KCl level showed a greater capacity for nitrate assimilation. The Pn was significantly and positively correlated with nitrate reductase (NR and glutamine synthetase (GS activities and was positively correlated with leaf-soluble protein and free amino acid (FAA contents. Both KCl starvation (0 mM and high KCl (40.00 mM led to water loss through a high transpiration rate and low water absorption, respectively, and resulted in increased concentrations of ursolic acid (UA, oleanolic acid (OA and flavonoids, with the exception of rosmarinic acid (RA. Moreover, the optimum concentration of KCl significantly increased the yields of RA, UA, OA and flavonoids. Our findings suggested that significantly higher plant biomass; chlorophyll content; Pn; stronger nitrogen anabolism; lower RA, UA, OA and flavonoid accumulation; and greater RA, UA, OA and flavonoid yields in P. vulgaris could be expected in the presence of the

Effect of potassium chloride supplementation in drinking water on broiler performance under heat stress conditions.

Science.gov (United States)

Ahmad, T; Khalid, T; Mushtaq, T; Mirza, M A; Nadeem, A; Babar, M E; Ahmad, G

2008-07-01

The effect of water supplementation of KCl on performance of heat-stressed Hubbard broilers was evaluated in the present experiment. The 3 experimental treatments (i.e., control, 0.3 and 0.6% KCl) were allocated to 3 replicates of 15 birds each. The control group was kept on dugout tap water, whereas the other 2 groups were supplied water supplemented with 0.3 and 0.6% KCl (wt/vol) by supplementing 3 and 6 g of KCl, respectively, per liter of drinking water. Broilers were provided ad libitum access to feed and water for the experimental period of 7 to 42 d of age and kept in open-sided house. The birds were reared under continuous thermostress (minimum 28.2 +/- 1.02 and maximum 37.5 +/- 0.78 degrees C) environment. Supplementing drinking water with 0.6% KCl reduced panting-phase blood pH to 7.31 and significantly increased live BW gain by 14.5 (P = 0.036) and 7.9% (P = 0.029) at 28 and 42 d of age, respectively, relative to control. An improved (P = 0.04) feed:gain and lowered body temperature were noted in groups supplemented with 0.6% KCl as compared with control and 0.3% KCl. Enhanced physiological adaptation with 0.6% KCl was evidenced by a more favorable pH during the panting phase in the present study. These findings demonstrated a possibility of better broiler live performance through KCl supplementation under conditions of severe heat stress (35 to 38 degrees C).

Effects of Sodium Chloride, Potassium Chloride and Calcium Chloride on the Formation of α-Dicarbonyl Compounds, Furfurals and Development of Browning in Cookies during Baking.

Science.gov (United States)

Kocadağlı, Tolgahan; Gökmen, Vural

2016-10-02

Effect of NaCl, KCl, CaCl2, NaHCO3, and NH4HCO3 on the formation of glucosone, 1-deoxyglucosone, 3-deoxyglucosone, glyoxal, methylglyoxal, diacetyl, 5-hydroxymethyl-2-furfural, 2-furfural and browning were investigated in cookies. Presence of 1.5% NaCl, 1% KCl, and 1% CaCl2 on flour basis had no effect on α-dicarbonyl compounds, except 1-deoxyglucosone increased in the presence of KCl and CaCl2. The increase in 5-hydroxymethyl-2-furfural formation in the presence of NaCl, KCl, and CaCl2 did not relate to 3-deoxyglucosone formation and pH changes. NaCl, KCl, and CaCl2 increased browning in cookies. Model reaction systems indicated that NaCl, KCl, and CaCl2 enhance browning by increasing furfurals in caramelization. NaCl, KCl, and CaCl2 decreased browning intensity in heated glucose-glycine system. Usage of CaCl2 in cookies may considerably increase furfurals but not α-dicarbonyl compounds. Sodium reduction can be obtained by replacement with potassium without sacrificing the desired consequences of caramelization in sugar rich bakeries.

Effects of lithium on extraction socket healing in rats assessed with micro-computed tomography.

Science.gov (United States)

Zeng, Yun Ting; Fu, Bin; Tang, Guo Hua; Zhang, Lei; Qian, Yu Fen

2013-09-01

Lithium is an activator of β-catenin signaling and β-catenin plays an important role in regulating bone formation and remodeling. The purpose of this study was to investigate the effects of lithium on bone repair in tooth extraction sockets in rats. Twenty male Wistar rats were subjected to maxillary left second molar extraction. The animals received a daily injection of lithium chloride (LiCl) or the same dose of sodium chloride (NaCl) starting 7 days before tooth extraction until sacrifice 14 days after extraction. Rats were randomly divided into: (1) a pre-treated group that received LiCl injection from 7 days before to 3 days after tooth extraction; (2) a post-treated group that received LiCl injection starting 4 days after tooth extraction; (3) a continuously treated group that received LiCl injection for the entire 21 days; and (4) a control group that received NaCl injection only. The volume of new bone and the bone density in the extraction socket were quantified by micro-computed tomography. The percentage of new bone formation in the extraction socket was as follows: 63.2 ± 13.4% (pre-treated group), 53.9 ± 9.8% (post-treated), 23.8 ± 8.0% (continuously treated) and 37.5 ± 4.2% (control). The difference in percentage was statistically significant between each pair of groups. Pre- and post-treated groups also showed a significant increase in the density of new bone. Lithium enhances bone repair in extraction sockets when delivered before or after tooth extraction. Tooth extraction during lithium treatment may impair bone healing.

A Simple Method for DNA Extraction from Mature Date Palm Leaves: Impact of Sand Grinding and Composition of Lysis Buffer

Science.gov (United States)

Arif, Ibrahim A.; Bakir, Mohammad A.; Khan, Haseeb A.; Ahamed, Anis; Al Farhan, Ahmad H.; Al Homaidan, Ali A.; Al Sadoon, Mohammad; Bahkali, Ali H.; Shobrak, Mohammad

2010-01-01

Molecular marker techniques have been widely used for cultivar identification of inbred date palms (Phoenix dactylifera L.; Arecaceae) and biodiversity conservation. Isolation of highly pure DNA is the prerequisite for PCR amplification and subsequent use such as DNA fingerprinting and sequencing of genes that have recently been developed for barcoding. To avoid problems related to the preservation and use of liquid nitrogen, we examined sterile sand for grinding the date palm leaves. Individual and combined effects of sodium chloride (NaCl), polyvinylpyrrolidone (PVP) and lithium chloride (LiCl) with the cetyltrimethylammonium bromide (CTAB) method for a DNA yield of sufficient purity and PCR amplification were evaluated in this study. Presence of LiCl and PVP alone or together in the lysis buffer did not significantly improve the DNA yield and purity compared with the addition of NaCl. Our study suggested that grinding of date palm leaf with sterile sand and inclusion of NaCl (1.4 M) in the lysis buffer without the costly use of liquid nitrogen, PVP and LiCl, provides a DNA yield of sufficient purity, suitable for PCR amplification. PMID:20957085

A Simple Method for DNA Extraction from Mature Date Palm Leaves: Impact of Sand Grinding and Composition of Lysis Buffer

Directory of Open Access Journals (Sweden)

Mohammad Al Sadoon

2010-09-01

Full Text Available Molecular marker techniques have been widely used for cultivar identification of inbred date palms (Phoenix dactylifera L.; Arecaceae and biodiversity conservation. Isolation of highly pure DNA is the prerequisite for PCR amplification and subsequent use such as DNA fingerprinting and sequencing of genes that have recently been developed for barcoding. To avoid problems related to the preservation and use of liquid nitrogen, we examined sterile sand for grinding the date palm leaves. Individual and combined effects of sodium chloride (NaCl, polyvinylpyrrolidone (PVP and lithium chloride (LiCl with the cetyltrimethylammonium bromide (CTAB method for a DNA yield of sufficient purity and PCR amplification were evaluated in this study. Presence of LiCl and PVP alone or together in the lysis buffer did not significantly improve the DNA yield and purity compared with the addition of NaCl. Our study suggested that grinding of date palm leaf with sterile sand and inclusion of NaCl (1.4 M in the lysis buffer without the costly use of liquid nitrogen, PVP and LiCl, provides a DNA yield of sufficient purity, suitable for PCR amplification.

Lithium chloride increases the production of amyloid-beta peptide independently from its inhibition of glycogen synthase kinase 3.

Science.gov (United States)

Feyt, Christine; Kienlen-Campard, Pascal; Leroy, Karelle; N'Kuli, Francisca; Courtoy, Pierre J; Brion, Jean-Pierre; Octave, Jean-Noël

2005-09-30

Glycogen synthase kinase 3 (GSK3) is able to phosphorylate tau at many sites that are found to be phosphorylated in paired helical filaments in Alzheimer disease. Lithium chloride (LiCl) efficiently inhibits GSK3 and was recently reported to also decrease the production of amyloid-beta peptide (Abeta) from its precursor, the amyloid precursor protein. Therefore, lithium has been proposed as a combined therapeutic agent, inhibiting both the hyperphosphorylation of tau and the production of Abeta. Here, we demonstrate that the inhibition of GSK3 by LiCl induced the nuclear translocation of beta-catenin in Chinese hamster ovary cells and rat cultured neurons, in which a decrease in tau phosphorylation was observed. In both cellular models, a nontoxic concentration of LiCl increased the production of Abeta by increasing the beta-cleavage of amyloid precursor protein, generating more substrate for an unmodified gamma-secretase activity. SB415286, another GSK3 inhibitor, induced the nuclear translocation of beta-catenin and slightly decreased Abeta production. It is concluded that the LiCl-mediated increase in Abeta production is not related to GSK3 inhibition.

Modeling Solute Thermokinetics in LiCI-KCI Molten Salt for Nuclear Waste Separation

Energy Technology Data Exchange (ETDEWEB)

Morgan, Dane; Eapen, Jacob

2013-10-01

at the eutectic composition (58 mol% LiCl, 42 mol% KCl), which is used for treating spent EBR-II fuel. The same process being used for EBRII fuel is currently being studied for widespread international implementation. The methods will focus on first-principles and first- principles derived interatomic potential based simulations, primarily using molecular dynamics. Results will be validated against existing literature and parallel ongoing experimental efforts. The simulation results will be of value for interpreting experimental results, validating analytical models, and for optimizing waste separation by potentially developing new salt configurations and operating conditions.

Investigating microstructural evolution during the electroreduction of UO{sub 2} to U in LiCl-KCl eutectic using focused ion beam tomography

Energy Technology Data Exchange (ETDEWEB)

Brown, L.D.; Abdulaziz, R.; Tjaden, B.; Inman, D.; Brett, D.J.L.; Shearing, P.R., E-mail: p.shearing@ucl.ac.uk

2016-11-15

Reprocessing of spent nuclear fuels using molten salt media is an attractive alternative to liquid-liquid extraction techniques. Pyroelectrochemical processing utilizes direct, selective, electrochemical reduction of uranium dioxide, followed by selective electroplating of a uranium metal. Thermodynamic prediction of the electrochemical reduction of UO{sub 2} to U in LiCl-KCl eutectic has shown to be a function of the oxide ion activity. The pO{sup 2−} of the salt may be affected by the microstructure of the UO{sub 2} electrode. A uranium dioxide filled “micro-bucket” electrode has been partially electroreduced to uranium metal in molten lithium chloride-potassium chloride eutectic. This partial electroreduction resulted in two distinct microstructures: a dense UO{sub 2} and a porous U metal structure were characterised by energy dispersive X-ray spectroscopy. Focused ion beam tomography was performed on five regions of this electrode which revealed an overall porosity ranging from 17.36% at the outer edge to 3.91% towards the centre, commensurate with the expected extent of reaction in each location. The pore connectivity was also seen to reduce from 88.32% to 17.86% in the same regions and the tortuosity through the sample was modelled along the axis of propagation of the electroreduction, which was seen to increase from a value of 4.42 to a value of infinity (disconnected pores). These microstructural characteristics could impede the transport of O{sup 2−} ions resulting in a change in the local pO{sup 2−} which could result in the inability to perform the electroreduction. - Highlights: • The microstructural evolution of the reduction from UO{sub 2} to U has been investigated. • The porosity and tortuosity is seen to change significantly during electroreduction. • Low porosity and high tortuosity associated with the UO{sub 2} phase may impede O{sup 2−} transport.

Two-dimensional high spatial-resolution dosimeter using europium doped potassium chloride: a feasibility study

International Nuclear Information System (INIS)

Li, H Harold; Yang, Deshan; Xiao, Zhiyan; Driewer, Joseph P; Han, Zhaohui; Low, Daniel A

2014-01-01

Recent research has shown that KCl:Eu 2+  has great potential for use in megavoltage radiation therapy dosimetry because this material exhibits excellent storage performance and is reusable due to strong radiation hardness. This work reports the authors’ attempts to fabricate 2D KCl:Eu 2+  storage phosphor films (SPFs) using both a physical vapor deposition (PVD) method and a tape casting method. X-ray diffraction analysis showed that a 10 µm thick PVD sample was composed of highly crystalline KCl. No additional phases were observed, suggesting that the europium activator had been completely incorporated into the KCl matrix. Photostimulated luminescence and photoluminescence spectra suggested that F (Cl − ) centers were the electron storage centers post x-ray irradiation and that Eu 2+  cations acted as luminescence centers in the photostimulation process. The 150 µm thick casted KCl:Eu 2+  SPF showed sub-millimeter spatial-resolution. Monte Carlo simulations further demonstrated that the admixture of 20% KCl:Eu 2+  and 80% low Z polymer binder exhibited almost no energy-dependence in a 6 MV beam. KCl:Eu 2+  pellet samples showed a large dynamic range from 0.01 cGy to 60 Gy dose-to-water, and saturated at approximately 500 Gy as a result of KCl's intrinsic high radiation hardness. Taken together, this work provides strong evidence that KCl:Eu 2+ -based SPF with associated readout apparatus could result in a novel electronic film system that has all the desirable features associated with classic radiographic film and, importantly, water equivalence and the capability of permanent identification of each detector. (paper)

Effect of short-term alkaline intervention on the performance of buffer-free single-chamber microbial fuel cell.

Science.gov (United States)

Yang, Na; Ren, Yueping; Li, Xiufen; Wang, Xinhua

2017-06-01

Anolyte acidification is a drawback restricting the electricity generation performance of the buffer-free microbial fuel cells (MFC). In this paper, a small amount of alkali-treated anion exchange resin (AER) was placed in front of the anode in the KCl mediated single-chamber MFC to slowly release hydroxyl ions (OH - ) and neutralize the H + ions that are generated by the anodic reaction in two running cycles. This short-term alkaline intervention to the KCl anolyte has promoted the proliferation of electroactive Geobacter sp. and enhanced the self-buffering capacity of the KCl-AER-MFC. The pH of the KCl anolyte in the KCl-AER-MFC increased and became more stable in each running cycle compared with that of the KCl-MFC after the short-term alkaline intervention. The maximum power density (P max ) of the KCl-AER-MFC increased from 307.5mW·m -2 to 542.8mW·m -2 , slightly lower than that of the PBS-MFC (640.7mW·m -2 ). The coulombic efficiency (CE) of the KCl-AER-MFC increased from 54.1% to 61.2% which is already very close to that of the PBS-MFC (61.9%). The results in this paper indicate that short-term alkaline intervention to the anolyte is an effective strategy to further promote the performance of buffer-free MFCs. Copyright © 2017 Elsevier B.V. All rights reserved.

The neuroprotective action of the mood stabilizing drugs lithium chloride and sodium valproate is mediated through the up-regulation of the homeodomain protein Six1

International Nuclear Information System (INIS)

Plant, Kathryn E.; Anderson, Elizabeth; Simecek, Nicole; Brown, Richard; Forster, Sam; Spinks, Jenny; Toms, Nick; Gibson, G. Gordon; Lyon, Jon; Plant, Nick

2009-01-01

The mood stabilizing agents lithium chloride (LiCl) and sodium valproate (VPA) have recently gained interest as potential neuroprotective therapeutics. However, exploitation of these therapeutic applications is hindered by both a lack of molecular understanding of the mode of action, and a number of sub-optimal properties, including a relatively small therapeutic window and variable patient response. Human neuroblastoma cells (SH-SY5Y) were exposed to 1 mM lithium chloride or 1 mM sodium valproate for 6 h or 72 h, and transcriptomes measured by Affymetrix U133A/B microarray. Statistically significant gene expression changes were identified using SAM software, with selected changes confirmed at transcript (TaqMan) and protein (Western blotting) levels. Finally, anti-apoptotic action was measured by an in vitro fluorescent assay. Exposure of SH-SY5Y cells to therapeutically relevant concentrations of either lithium chloride or sodium valproate elicited 936 statistically significant changes in gene expression. Amongst these changes we observed a large (maximal 31.3-fold) increase in the expression of the homeodomain protein Six1, and have characterized the time- and dose-dependent up-regulation of this gene in response to both drugs. In addition, we demonstrate that, like LiCl or VPA treatment, Six1 over-expression protects SH-SY5Y cells from staurosporine-induced apoptosis via the blockade of caspsase-3 activation, whereas removal of Six1 protein via siRNA antagonises the ability of LiCl and VPA to protect SH-SY5Y cells from STS-induced apoptosis. These results provide a novel mechanistic rationale underlying the neuroprotective mechanism of LiCl and VPA, suggesting exciting possibilities for the development of novel therapeutic agents against neurodegenerative diseases such as Alzheimer's or Parkinsonism

Lithium increases ammonium excretion leading to altered urinary acid-base buffer composition.

Science.gov (United States)

Trepiccione, Francesco; Altobelli, Claudia; Capasso, Giovambattista; Christensen, Birgitte Mønster; Frische, Sebastian

2017-11-24

Previous reports identify a voltage dependent distal renal tubular acidosis (dRTA) secondary to lithium (Li + ) salt administration. This was based on the inability of Li + -treated patients to increase the urine-blood (U-B) pCO 2 when challenged with NaHCO 3 and, the ability of sodium neutral phosphate or Na 2 SO 4 administration to restore U-B pCO 2 in experimental animal models. The underlying mechanisms for the Li + -induced dRTA are still unknown. To address this point, a 7 days time course of the urinary acid-base parameters was investigated in rats challenged with LiCl, LiCitrate, NaCl, or NaCitrate. LiCl induced the largest polyuria and a mild metabolic acidosis. Li + -treatment induced a biphasic response. In the first 2 days, proper urine volume and acidification occurred, while from the 3rd day of treatment, polyuria developed progressively. In this latter phase, the LiCl-treated group progressively excreted more NH 4 + and less pCO 2 , suggesting that NH 3 /NH 4 + became the main urinary buffer. This physiological parameter was corroborated by the upregulation of NBCn1 (a marker of increased ammonium recycling) in the inner stripe of outer medulla of LiCl treated rats. Finally, by investigating NH 4 + excretion in ENaC-cKO mice, a model resistant to Li + -induced polyuria, a primary role of the CD was confirmed. By definition, dRTA is characterized by deficient urinary ammonium excretion. Our data question the presence of a voltage-dependent Li + -induced dRTA in rats treated with LiCl for 7 days and the data suggest that the alkaline urine pH induced by NH 3 /NH 4 + as the main buffer has lead to the interpretation dRTA in previous studies.

Membrane-Based Osmotic Heat Engine with Organic Solvent for Enhanced Power Generation from Low-Grade Heat

Energy Technology Data Exchange (ETDEWEB)

Shaulsky, E; Boo, C; Lin, SH; Elimelech, M

2015-05-05

We present a hybrid osmotic heat engine (OHE) system that uses draw solutions with an organic solvent for enhanced thermal separation efficiency. The hybrid OHE system produces sustainable energy by combining pressure-retarded osmosis (PRO) as a power generation stage and membrane distillation (MD) utilizing low-grade heat as a separation stage. While previous OHE systems employed aqueous electrolyte draw solutions, using methanol as a solvent is advantageous because methanol is highly volatile and has a lower heat capacity and enthalpy of vaporization than water. Hence, the thermal separation efficiency of a draw solution with methanol would be higher than that of an aqueous draw solution. In this study, we evaluated the performance of LiCl-methanol as a potential draw solution for a PRO-MD hybrid OHE system. The membrane transport properties as well as performance with LiCl methanol draw solution were evaluated using thin-film composite (TFC) PRO membranes and compared to the results obtained with a LiCl water draw solution. Experimental PRO methanol flux and maximum projected power density of 47.1 L m(-2) h(-1) and 72.1 W m(-2), respectively, were achieved with a 3 M LiCl-methanol draw solution. The overall efficiency of the hybrid OHE system was modeled by coupling the mass and energy flows between the thermal separation (MD) and power generation (PRO) stages under conditions with and without heat recovery. The modeling results demonstrate higher ORE energy efficiency with the LiCl methanol draw solution compared to that with the LiCl water draw solution under practical operating conditions (i.e., heat recovery <90%). We discuss the implications of the results for converting low-grade heat to power.

Enhanced Chondrogenic Differentiation of Human Umbilical Cord Wharton's Jelly Derived Mesenchymal Stem Cells by GSK-3 Inhibitors.

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Prapot Tanthaisong

Full Text Available Articular cartilage is an avascular, alymphatic, and aneural system with very low regeneration potential because of its limited capacity for self-repair. Mesenchymal stem cells (MSCs are the preferred choice for cell-based therapies. Glycogen synthase kinase 3 (GSK-3 inhibitors are compounds that can induce the Wnt signaling pathway, which is involved in chondrogenesis and cartilage development. Here, we investigated the influence of lithium chloride (LiCl and SB216763 synergistically with TGF-β3 on chondrogenic differentiation in human mesenchymal stem cells derived from Wharton's jelly tissue (hWJ-MSCs. hWJ-MSCs were cultured and chondrogenic differentiation was induced in monolayer and pellet experiments using chondrogenic medium, chondrogenic medium supplemented with LiCl, or SB216763 for 4 weeks. After in vitro differentiation, cultured cells were examined for the expression of Sox9, ACAN, Col2a1, and β-catenin markers. Glycosaminoglycan (GAG accumulation was also examined by Alcian blue staining. The results indicated that SB216763 was more effective than LiCl as evidenced by a higher up-regulation of the expression of cartilage-specific markers, including Sox9, ACAN, Col2a1 as well as GAG accumulation. Moreover, collagen type II expression was strongly observed in cells cultured in the chondrogenic medium + SB216763 as evidenced by western blot analysis. Both treatments appeared to mediate the Wnt signaling pathway by up-regulating β-catenin gene expression. Further analyses showed that all treatments suppressed the progression of chondrocyte hypertrophy, determined by decreased expression of Col10a1 and Runx2. These results indicate that LiCl and SB216763 are potential candidates for further in vivo therapeutic trials and would be of great importance for cartilage regeneration.

Thermal and optical properties of Tm3+ doped tellurite glasses.

Science.gov (United States)

Ozen, G; Demirata, B; Oveçoğlu, M L; Genç, A

2001-02-01

Ultraviolet, visible (UV/VIS) and differential thermal analysis (DTA) measurements were carried out in order to investigate the optical and thermal properties of various 0.5 mol.% Tm2O3 containing (1 - x)TeO2 + xLiCl glasses in molar ratio. The samples were prepared by fusing the mixture of their respective reagent grade powders in a platinum cricuble at 750 degrees C for 30 min. DTA curves taken in the 23-600 degrees C temperature range with a heating rate of 10 degrees C/min reveal a change in the value of the glass transition temperature, Tg, while melting was not observed for the glasses containing LiCl content less than 50 mol.%. These glasses were found to be moisture-resistant. However, the glasses with LiCl content higher than 50 mol.%, in which a melting peak was observed at Tc = 401 degrees C, were moisture-sensitive. Absorption measurements in the UV/VIS region of the glasses without Tm2O3 content show that the Urbach cutoff occurs at about 320 nm and, is relatively independent of the LiCl content. Six absorption bands were observed in the Tm2O3 doped glasses corresponding to the absorption of the 1G4, 3F2, 3F3 and 3F4, 3H5 and 3H4 levels from the 3H6 ground level of Tm3+ ions. The spectra also show that the integrated absorption cross-section of each band depends on the glass composition. Judd-Ofelt theory was used to determine the Judd-Ofelt parameters as well as the radiative transition probabilities for the metastable levels of Tm3+ ions in (0.3)LiCl + (0.7) TeO2: 0.01 Tm2O3 glass which is moisture-resistant.

Development of a novel smoke-flavoured salmon product by sodium replacement using water vapour permeable bags.

Science.gov (United States)

Rizo, Arantxa; Fuentes, Ana; Barat, José M; Fernández-Segovia, Isabel

2018-05-01

Food manufacturers need to reduce sodium content to meet consumer and public health demands. In the present study, the use of sodium-free (SF) salt and KCl to develop a novel smoke-flavoured salmon product with reduced sodium content was evaluated. Fifty percent of NaCl was replaced with 50% of SF salt or 50% KCl in the salmon smoke-flavouring process, which was carried out using water vapour permeable bags. Triangle tests showed that samples with either SF salt or KCl were statistically similar to the control samples (100% NaCl). Because no sensorial advantage in using SF salt was found compared to KCl and given the lower price of KCl, the KCl-NaCl samples were selected for the next phase. The changes of physicochemical and microbial parameters in smoke-flavoured salmon during 42 days showed that partial replacement of NaCl with KCl did not significantly affect the quality and shelf-life of smoke-flavoured salmon, which was over 42 days. Smoke-flavoured salmon with 37% sodium reduction was developed without affecting the sensory features and shelf-life. This is an interesting option for reducing the sodium content in such products to help meet the needs set by both health authorities and consumers. © 2017 Society of Chemical Industry. © 2017 Society of Chemical Industry.

Production of Long-Lived H2-, HD-, and D2- during Grazing Scattering Collisions of H2+, H3+, D2+, D3+ and D2H+ Ions with KBr, KCl, and LiF Surfaces

International Nuclear Information System (INIS)

Seely, D. G.; Meyer, F. W.; Zhang, H.; Havener, C. C.

2009-01-01

We have investigated atomic and molecular anion production from singly charged atomic and molecular hydrogen, deuterium, and mixed isotope beams during grazing interactions with large area KBr, KCl, and LiF single crystal targets in the incident energy range 4-22.5 keV. Electron capture and, in the case of incident molecular ions, dissociation occur during the grazing interactions without appreciable angular straggling or change in velocity. As a result, atomic and molecular cation and anion interaction products are strongly peaked in the specular reflection direction, and, in case of dissociation products, at the fractional kinetic energies determined by the product fragment mass to incident mass ratios. A large-acceptance electrostatic analysis and detection system is used to collect the charged scattering products with high efficiency. Of particular interest is the production of metastable molecular ions H 2 - , HD - , and D 2 - . By comparing molecular anion yields obtained from incident hydrogen, deuterium and mixed isotope molecular ions, effects arising from isobaric contamination are seen for some incident molecular species.

New insights into negative effects of lithium on sea urchin Paracentrotus lividus embryos

Science.gov (United States)

Ruocco, Nadia; Costantini, Maria; Santella, Luigia

2016-01-01

The diffuse use of lithium in a number of industrial processes has produced a significant contamination of groundwater and surface water with it. The increased use of lithium has generated only scarce studies on its concentrations in ambient waters and on its effects on aquatic organisms. Only few contributions have focused on the toxicity of lithium in marine organisms (such as marine animals, algae and vegetables), showing that the toxic effect depends on the animal species. In the present study we describe the morphological and the molecular effects of lithium chloride (LiCl), using the sea urchin Paracentrotus lividus as a model organism. We show that LiCl, if added to the eggs before fertilization, induces malformations in the embryos in a dose-dependent manner. We have also followed by RT qPCR the expression levels of thirty seven genes (belonging to different classes of functional processes, such as stress, development, differentiation, skeletogenesis and detoxifications) to identify the molecular targets of LiCl. This study opens new perspectives for the understanding of the mechanism of action of lithium on marine organisms. The findings may also have relevance outside the world of marine organisms since lithium is widely prescribed for the treatment of human bipolar disorders. PMID:27562248

Thermochemical Characterizations of Novel Vermiculite-LiCl Composite Sorbents for Low-Temperature Heat Storage

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Yannan Zhang

2016-10-01

Full Text Available To store low-temperature heat below 100 °C, novel composite sorbents were developed by impregnating LiCl into expanded vermiculite (EVM in this study. Five kinds of composite sorbents were prepared using different salt concentrations, and the optimal sorbent for application was selected by comparing both the sorption characteristics and energy storage density. Textural properties of composite sorbents were obtained by extreme-resolution field emission scanning electron microscopy (ER-SEM and an automatic mercury porosimeter. After excluding two composite sorbents which would possibly exhibit solution leakage in practical thermal energy storage (TES system, thermochemical characterizations were implemented through simulative sorption experiments at 30 °C and 60% RH. Analyses of thermogravimetric analysis/differential scanning calorimetry (TGA/DSC curves indicate that water uptake of EVM/LiCl composite sorbents is divided into three parts: physical adsorption of EVM, chemical adsorption of LiCl crystal, and liquid–gas absorption of LiCl solution. Energy storage potential was evaluated by theoretical calculation based on TGA/DSC curves. Overall, EVMLiCl20 was selected as the optimal composite sorbent with water uptake of 1.41 g/g, mass energy storage density of 1.21 kWh/kg, and volume energy storage density of 171.61 kWh/m3.

Electrodeposition Behavior of U into Liquid Cd Cathode at Low Current Density

International Nuclear Information System (INIS)

Kim, Si Hyung; Kim, Gha-Young; Sim, Jun-Bo; Paek, Seungwoo; Ahn, Do-Hee

2015-01-01

According to the U-Cd phase diagram, U and UCd 11 are, respectively, present as a stable phase above and below 473 .deg. C when both U and Cd elements coexist at such temperatures. U metals deposited on the surface of the LCC around 500 .deg. C tends to form a dendrite shape having a large surface area and the U dendrites floating on the surface of the LCC have a role of a solid cathode, and from that time, co-deposition of U and TRU can be hampered. If the UCd 11 phase does not have a dendrite form during electrodeposition, this phase may sink into the liquid Cd. This can be a good method to simplify the equipment configuration through the omission of the stirring tool. In this study, the deposition behavior of U metal was observed when electrodeposition using a LCC was carried out at 450 and 500 .deg. C at low current density. To observe the deposition behavior of U when using a liquid cadmium cathode (LCC), several deposition experiments were conducted in the LiCl- KCl-UCl 3 salt at a current density of 50 mA/cm 2 at 450 and 500 .deg.C. At 500 .deg. C, the U metal deposited on the LCC grew in the form of a dendrite shape having a large surface area, and thus it was not sunk into the liquid Cd even though the density of U was much larger than that of liquid Cd. On the other hand, the UCd 11 phase was stable according to the U-Cd phase diagram at 450 .deg. C

Uso da vinhaça no abacaxizeiro em solo de baixo potencial de produção Stillage application for pineapple in soil with low potential of yield

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Miralda Bueno de Paula

1999-07-01

Full Text Available O trabalho foi desenvolvido com o objetivo de avaliar a vinhaça como fonte de K para o abacaxizeiro (Ananas Comosus L., em substituição ao KCl, e seus efeitos sobre as características químicas do solo. O experimento foi instalado em um LV, textura argilosa, utilizando a cv. Smooth Cayenne. Os tratamentos constaram de quatro doses de vinhaça (0 - 100 - 200 - 400 m³/ha, mais um tratamento adicional: 12 g/planta K2O (KCl. O delineamento experimental foi em blocos ao acaso, com três repetições. Verificou-se efeito significativo da vinhaça e do KCl sobre a produção. Com 400 m³/ha de vinhaça e 20,5 g/planta de KCl , os rendimentos tiveram um acréscimo de 70% e 73%, respectivamente, em relação à testemunha. O fornecimento de K elevou a porcentagem de acidez titulável total e sólidos solúveis totais nos frutos, porém não houve diferença significativa entre as fontes. Os teores foliares de K foram aumentados significativamente pela aplicação de vinhaça e de KCl, e os teores de Mg decresceram. A aplicação de vinhaça contribuiu para aumento, no solo, dos teores dos cátions K, Ca, Mg e para a lixiviação de K. Vinhaça e KCl elevaram a níveis adequados, para cultura, a porcentagem de K na soma de bases.An experiment was carried out in order to evaluate the stillage as K source for pineapple (Ananas Comosus L. in comparison with KCl, and the effects on chemical soil characteristics. The experiment was assessed in a Red Yellow Latosol with Smooth Cayenne cultivar. The treatments consisted of four application doses of stillage (0 - 100 - 200 - 400 m³/ha and of an additional treatment (12 g/plant K2O KCl. The design of the trial was in randomized blocks with three replications. Yields statistically responded to stillage and KCl and yields obtained with 400 m³/ha of stillage and 20.5 g of KCl per plant were 70% and 73%, respectivelly, over the control. Addition of K increased the content of tritratable acidity and total

Electrodeposition of ZnO from DMSO solution: influence of anion nature and its concentration in the nucleation and growth mechanisms

Energy Technology Data Exchange (ETDEWEB)

Riveros, Gonzalo; Ramirez, Daniel, E-mail: gonzalo.riveros@uv.cl [Departamento de Quimica y Bioquimica, Facultad de Ciencias, Universidad de Valparaiso, Valparaiso (Chile); Tello, Alejandra; Schrebler, Ricardo; Henriquez, Rodrigo; Gomez, Humberto [Instituto de Quimica, Pontificia Universidad Catolica de Valparaiso, Curauma, Valparaiso (Chile)

2012-03-15

The influence of the anion nature and its concentration in the electrodeposition of ZnO onto a gold electrode from dimethylsulfoxide (DMSO) solutions was studied. Voltammetric experiments revealed important changes in the zinc oxide electrodeposition process depending on the employed anion as electrolyte. From chronoamperometric experiments, the corresponding current-time curves were fitted with different nucleation and growth mechanism models. The analysis of these results showed changes from an instantaneous to a progressive growth when the solution composition was changed from ZnCl{sub 2} to ZnCl{sub 2} + LiCl. The change of the mechanism is associated to the adsorption of chloride ion on the active sites of the electrode surface when LiCl is present in the solution. (author)

Is there a potential consumer market for low-sodium fermented sausages?

Science.gov (United States)

Dos Santos, Bibiana A; Campagnol, Paulo C B; da Cruz, Adriano G; Morgano, Marcelo A; Wagner, Roger; Pollonio, Marise A R

2015-05-01

The NaCl levels in dry fermented sausages were reduced by 50% or were substituted with KCl, CaCl2 , or a blend of KCl and CaCl2 (1:1). The quality, safety, and the potential consumer market of dry fermented sausages were assessed. Neither 50% reduction of the NaCl content nor the substitution of 50% of the NaCl with KCl influenced the fermentation and maturation process. However, when CaCl2 was used as the substitute salt (50%), there was a significant decrease in pH, an increase in the water activity, and a decrease in lactic acid and micrococcus bacterial counts. Overall, the sensory acceptance decreased in dry fermented sausages with reduced sodium content. However, cluster analysis and internal preference mapping revealed potential for commercialization of samples with 50% of the NaCl content substituted with KCl or with a mixture of KCl and CaCl2 (1:1). © 2015 Institute of Food Technologists®

Chemical Reduction of SIM MOX in Molten Lithium Chloride Using Lithium Metal Reductant

Science.gov (United States)

Kato, Tetsuya; Usami, Tsuyoshi; Kurata, Masaki; Inoue, Tadashi; Sims, Howard E.; Jenkins, Jan A.

2007-09-01

A simulated spent oxide fuel in a sintered pellet form, which contained the twelve elements U, Pu, Am, Np, Cm, Ce, Nd, Sm, Ba, Zr,Mo, and Pd, was reduced with Li metal in a molten LiCl bath at 923 K. More than 90% of U and Pu were reduced to metal to form a porous alloy without significant change in the Pu/U ratio. Small fractions of Pu were also combined with Pd to form stable alloys. In the gap of the porous U-Pu alloy, the aggregation of the rare-earth (RE) oxide was observed. Some amount of the RE elements and the actinoides leached from the pellet. The leaching ratio of Am to the initially loaded amount was only several percent, which was far from about 80% obtained in the previous ones on simple MOX including U, Pu, and Am. The difference suggests that a large part of Am existed in the RE oxide rather than in the U-Pu alloy. The detection of the RE elements and actinoides in the molten LiCl bath seemed to indicate that they dissolved into the molten LiCl bath containing the oxide ion, which is the by-product of the reduction, as solubility of RE elements was measured in the molten LiCl-Li2O previously.

Effects of Additives on the Morphology and Performance of PPTA/PVDF in Situ Blend UF Membrane

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Hong-Bin Li

2014-06-01

Full Text Available Poly(p-phenylene terephtalamide (PPTA, a high-performance polymer with high modulus and good hydrophilicity, is often used as a reinforced material. However, due to its high crystallity, micro-phase separation often occurs in the blends. In this paper, PPTA/poly(vinylidene fluoride (PVDF compatible blend solution was synthesized by in situ polycondensation. Blend ultra-filtration membrane was prepared through the immersion phase inversion process. In order to obtain desired pore structure, the effects of different additives including hydrophilic polymer (polyethylene glycol (PEG, inorganic salt (lithium chloride (LiCl and the surfactant (Tween-80 on the morphology and performance of PPTA/PVDF blend membranes were studied. The membrane formation process was investigated through ternary phase diagram (thermodynamics and viscosities (kinetics analysis. It was found that, with the increasing of LiCl content, a porous membrane structure with long finger-like pores was formed due to the accelerated demixing process which resulted in the increase of porosity and pore diameter as well as the enhancement of water flux and the decline of PEG rejection. When Tween content increased to over 3 wt%, dynamic viscosity became the main factor resulting in a decreased phase separation rate. The transfer of PEG and LiCl molecules onto membrane surface increased the surface hydrophilicity. The effect of Tween content on membrane hydrophilicity was also correlated with the compatibility of blend components.

Electron-stimulated desorption of lithium ions from lithium halide thin films

International Nuclear Information System (INIS)

Markowski, Leszek

2007-01-01

Electron-stimulated desorption of positive lithium ions from thin layers of lithium halides deposited onto Si(1 1 1) are investigated by the time-of-flight technique. The determined values of isotope effect of the lithium ( 6 Li + / 7 Li + ) are 1.60 ± 0.04, 1.466 ± 0.007, 1.282 ± 0.004, 1.36 ± 0.01 and 1.33 ± 0.01 for LiH, LiF, LiCl, LiBr and LiI, respectively. The observed most probable kinetic energies of 7 Li + are 1.0, 1.9, 1.1, 0.9 and 0.9 eV for LiH, LiF, LiCl, LiBr and LiI, respectively, and seem to be independent of the halide component mass. The values of lithium ion emission yield, lithium kinetic energy and lithium isotope effect suggest that the lattice relaxation is only important in the lithium ion desorption process from the LiH system. In view of possible mechanisms and processes involved into lithium ion desorption the obtained results indicate that for LiH, LiCl, LiBr and LiI the ions desorb in a rather classical way. However, for LiF, ion desorption has a more quantum character and the modified wave packet squeezing model has to be taken into account

Glycogen Synthase Kinase 3β Inhibition as a Therapeutic Approach in the Treatment of Endometrial Cancer

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Liang Ma

2013-08-01

Full Text Available Alternative strategies beyond current chemotherapy and radiation therapy regimens are needed in the treatment of advanced stage and recurrent endometrial cancers. There is considerable promise for biologic agents targeting the extracellular signal-regulated kinase (ERK pathway for treatment of these cancers. Many downstream substrates of the ERK signaling pathway, such as glycogen synthase kinase 3β (GSK3β, and their roles in endometrial carcinogenesis have not yet been investigated. In this study, we tested the importance of GSK3β inhibition in endometrial cancer cell lines and in vivo models. Inhibition of GSK3β by either lithium chloride (LiCl or specific GSK3β inhibitor VIII showed cytostatic and cytotoxic effects on multiple endometrial cancer cell lines, with little effect on the immortalized normal endometrial cell line. Flow cytometry and immunofluorescence revealed a G2/M cell cycle arrest in both type I (AN3CA, KLE, and RL952 and type II (ARK1 endometrial cancer cell lines. In addition, LiCl pre-treatment sensitized AN3CA cells to the chemotherapy agent paclitaxel. Administration of LiCl to AN3CA tumor-bearing mice resulted in partial or complete regression of some tumors. Thus, GSK3β activity is associated with endometrial cancer tumorigenesis and its pharmacologic inhibition reduces cell proliferation and tumor growth.

Aversion learning can reduce meal size without taste avoidance in rats.

Science.gov (United States)

Tracy, Andrea L; Schurdak, Jennifer D; Chambers, James B; Benoit, Stephen C

2016-03-01

Nausea and aversive food responses are commonly reported following bariatric surgery, along with post-surgical reduction in meal size. This study investigates whether a meal size limit can be conditioned by associating large meals with aversive outcomes. In rats, the intake of meals exceeding a pre-defined size threshold was paired with lithium chloride-induced gastric illness, and the effects on self-determined food intakes and body weight were measured. Rats given LiCl contingent on the intake of a large meal learned to reliably reduce intake below this meal size threshold, while post-meal saline or LiCl before meals did not change meal size. It was further demonstrated that this is not a conditioned taste aversion and that this effect transferred to foods not explicitly trained. Finally, when rats received LiCl following all large meals, the number of small meals increased, but total food intake and body weight decreased. While further work is needed, this is the first demonstration that meal size may be conditioned, using an aversion procedure, to remain under a target threshold and that this effect is distinct from taste avoidance. Corresponding reduction in food intake and body weight suggests that this phenomenon may have implications for developing weight loss strategies and understanding the efficacy of bariatric surgery. © 2016 The Obesity Society.

Influence of partial replacement of sodium chloride by potassium chloride in Minas fresh cheese of sheep’s milk

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Dalana Cecília Hanauer

2017-08-01

Full Text Available The sheep’s milk has high contents of fat, protein and minerals in relation to the cow’s milk and is suitable for the production of cheeses, as the Minas fresh. The production of this cheese includes the salting, by offering important functions for this product. The salting is performed by adding sodium chloride (NaCl, however in excess this salt may be harmful to consumer health. Then, it was evaluated the development of tree formulations of Minas fresh cheese sheep’s milk (100% NaCl – QA; 75% NaCl and 25% potassium chloride (KCl – QB; 50% NaCl and 50% KCl – QC and they were evaluated by physical-chemical, microbiological and sensorial analyzes. A partial replacement of NaCl by KCl did not influence the moisture, protein and ash contents, pH and water activity of the cheeses. Furthermore, a 50% substitution of NaCl by KCl enabled to obtain a cheese with reduced sodium content in relation to the standard with 100% NaCl. The sensorial analysis showed that the substitution of 50% (QC and 25% (QB of NaCl by KCl did not show significant for the overall acceptance index, however, the use of KCl was perceived by the evaluators, since the formulations QB and QC differed significantly from the standard (QA. However, in the multiple comparison test there was no significant difference between the samples. Thus, the results indicated that a partial replacement of NaCl by KCl can be performed at Minas fresh cheese from sheep’smilk.

Development of flexible, free-standing, thin films for additive manufacturing and localized energy generation

Energy Technology Data Exchange (ETDEWEB)

Clark, Billy; McCollum, Jena; Pantoya, Michelle L., E-mail: michelle.pantoya@ttu.edu [Mechanical Engineering Department, Texas Tech University, Lubbock TX 79409 (United States); Heaps, Ronald J.; Daniels, Michael A. [Idaho National Laboratory, PO Box 1625, Idaho Falls, ID 83415 (United States)

2015-08-15

Film energetics are becoming increasingly popular because a variety of technologies are driving a need for localized energy generation in a stable, safe and flexible form. Aluminum (Al) and molybdenum trioxide (MoO{sub 3}) composites were mixed into a silicon binder and extruded using a blade casting technique to form flexible free-standing films ideal for localized energy generation. Since this material can be extruded onto a surface it is well suited to additive manufacturing applications. This study examines the influence of 0-35% by mass potassium perchlorate (KClO{sub 4}) additive on the combustion behavior of these energetic films. Without KClO{sub 4} the film exhibits thermal instabilities that produce unsteady energy propagation upon reaction. All films were cast at a thickness of 1 mm with constant volume percent solids to ensure consistent rheological properties. The films were ignited and flame propagation was measured. The results show that as the mass percent KClO{sub 4} increased, the flame speed increased and peaked at 0.43 cm/s and 30 wt% KClO{sub 4}. Thermochemical equilibrium simulations show that the heat of combustion increases with increasing KClO{sub 4} concentration up to a maximum at 20 wt% when the heat of combustion plateaus, indicating that the increased chemical energy liberated by the additional KClO{sub 4} promotes stable energy propagation. Differential scanning calorimeter and thermogravimetric analysis show that the silicone binder participates as a fuel and reacts with KClO{sub 4} adding energy to the reaction and promoting propagation.

Development of flexible, free-standing, thin films for additive manufacturing and localized energy generation

Directory of Open Access Journals (Sweden)

Billy Clark

2015-08-01

Full Text Available Film energetics are becoming increasingly popular because a variety of technologies are driving a need for localized energy generation in a stable, safe and flexible form. Aluminum (Al and molybdenum trioxide (MoO3 composites were mixed into a silicon binder and extruded using a blade casting technique to form flexible free-standing films ideal for localized energy generation. Since this material can be extruded onto a surface it is well suited to additive manufacturing applications. This study examines the influence of 0-35% by mass potassium perchlorate (KClO4 additive on the combustion behavior of these energetic films. Without KClO4 the film exhibits thermal instabilities that produce unsteady energy propagation upon reaction. All films were cast at a thickness of 1 mm with constant volume percent solids to ensure consistent rheological properties. The films were ignited and flame propagation was measured. The results show that as the mass percent KClO4 increased, the flame speed increased and peaked at 0.43 cm/s and 30 wt% KClO4. Thermochemical equilibrium simulations show that the heat of combustion increases with increasing KClO4 concentration up to a maximum at 20 wt% when the heat of combustion plateaus, indicating that the increased chemical energy liberated by the additional KClO4 promotes stable energy propagation. Differential scanning calorimeter and thermogravimetric analysis show that the silicone binder participates as a fuel and reacts with KClO4 adding energy to the reaction and promoting propagation.

Nitrogen fertilization efficiency with Urea ({sup 15}N) in Brachiaria brizantha cv. Marandu associated with split application of ordinary superphosphate and potassium chloride; Eficiencia da fertilizacao nitrogenada com ureia ({sup 15}N) em Brachiaria brizantha cv. Marandu associada ao parcelamento de superfosfato simples e cloreto de potassio

Energy Technology Data Exchange (ETDEWEB)

Oliveira, P.P.A. [EMBRAPA, Pirassununga, SP (Brazil). Centro Nacional de Pesquisa de Gado e Leite]. E-mail: ppaolive@cnpgl.embrapa.br; Trivelin, P.C.O. [Centro de Energia Nuclear na Agricultura (CENA), Piracicaba, SP (Brazil). Lab. de Isotopos Estaveis]. E-mail: pcotrive@cena.usp.br; Oliveira, W.S. [Centro de Energia Nuclear na Agricultura (CENA), Piracicaba, SP (Brazil). Lab. de Biologia Celular e Molecular]. E-mail: wsolivei@carpa.ciagri.usp.br

2003-08-01

In pastures, the evaluation of fertilization efficiency of urea-N is important since it is applied on a massive scale. Several studies report an enhancement of the fertilizers efficiency by associated applications of urea with potassium chloride (KCl) and ordinary superphosphate (OSP). In the recovery of degraded pastures or in intensive exploration systems, high quantities of KCl and OSP used as corrective fertilization are applied at the november, beginning of the rain season. Split applications of KCl and OSP could easily be associated with urea-N surface application without additional costs. An evaluation of this management was the objective of this experiment. The annual balance of {sup 15} N application with urea was obtained in treatments where OSP and/or KCl were split, top-dressed in five applications associated with urea, or when both were applied together in November. Highest forage production was obtained when OSP was split, followed by split KCl, the unique application of both together, and finally both split. The recovery of urea-N in the aerial part and the soil-pasture system remained unaltered by the treatments. However, the recovery of plant crown and root system differed among the treatments and was positively correlated with forage production. Fertilizer-N recovery in the litter was favored by splitting KCl. Even though the total recovery of the system was not improved by the treatments, splitting of KCl and OSP are indicated for an increased recovery of urea-N in numerous plant structures, resulting in a higher forage production. (author)

Nitrogen fertilization efficiency with Urea (15N) in Brachiaria brizantha cv. Marandu associated with split application of ordinary superphosphate and potassium chloride

International Nuclear Information System (INIS)

Oliveira, P.P.A.; Trivelin, P.C.O.; Oliveira, W.S.

2003-01-01

In pastures, the evaluation of fertilization efficiency of urea-N is important since it is applied on a massive scale. Several studies report an enhancement of the fertilizers efficiency by associated applications of urea with potassium chloride (KCl) and ordinary superphosphate (OSP). In the recovery of degraded pastures or in intensive exploration systems, high quantities of KCl and OSP used as corrective fertilization are applied at the november, beginning of the rain season. Split applications of KCl and OSP could easily be associated with urea-N surface application without additional costs. An evaluation of this management was the objective of this experiment. The annual balance of 15 N application with urea was obtained in treatments where OSP and/or KCl were split, top-dressed in five applications associated with urea, or when both were applied together in November. Highest forage production was obtained when OSP was split, followed by split KCl, the unique application of both together, and finally both split. The recovery of urea-N in the aerial part and the soil-pasture system remained unaltered by the treatments. However, the recovery of plant crown and root system differed among the treatments and was positively correlated with forage production. Fertilizer-N recovery in the litter was favored by splitting KCl. Even though the total recovery of the system was not improved by the treatments, splitting of KCl and OSP are indicated for an increased recovery of urea-N in numerous plant structures, resulting in a higher forage production. (author)

TH-C-19A-12: Two-Dimensional High Spatial-Resolution Dosimeter Using Europium Doped Potassium Chloride

International Nuclear Information System (INIS)

Li, H; Yang, D; Xiao, Z; Driewer, J; Han, Z; Low, D

2014-01-01

Purpose: Recent research has shown that KCl:Eu2+ has great potential for use in megavoltage radiation therapy dosimetry because this material exhibits excellent storage performance and is reusable due to strong radiation hardness. This work reports our attempts to fabricate 2D KCl:Eu2+ storage phosphor films (SPFs) using both a physical vapor deposition (PVD) method and a tape casting method. Methods: A thin layer of KCl:Eu2+ was deposited on a substrate of borosilicate glass (e.g., laboratory slides) with a PVD system. For tape casting, a homogenous suspension containing storage phosphor particles, liquid vehicle and polymer binder was formed and subsequently cast by doctor-blade onto a polyethylene terephthalate substrate to form a 150 μm thick SPF. Results: X ray diffraction analysis showed that a 10 μm thick PVD sample was composed of highly crystalline KCl. No additional phases were observed, suggesting that the europium activator had completed been incorporated into the KCl matrix. Photostimulated luminescence and photoluminescence spectra suggested that F (Cl−) centers were the electron storage centers post x ray irradiation and that Eu2+ cations acted as luminescence centers in the photostimulation process. The 150 μm thick casted KCl:Eu2+ SPF showed sub-millimeter spatial resolution. Monte Carlo simulations further demonstrated that the admixture of 20% KCl:Eu2+ and 80% low Z polymer binder exhibited almost no energy dependence in a 6 MV beam. KCl:Eu2+ pellet samples showed a large dynamic range from 0.01 cGy to 60 Gy dose-to-water, and saturated at approximately 500 Gy as a Result of its intrinsic high radiation hardness. Conclusions: This discovery research provides strong evidence that KCl:Eu2+ based SPF with associated readout apparatus could Result in a novel electronic film system that has all the desirable features associated with classic radiographic film and, importantly, water equivalence and the capability of permanent identification of

TH-C-19A-12: Two-Dimensional High Spatial-Resolution Dosimeter Using Europium Doped Potassium Chloride

Energy Technology Data Exchange (ETDEWEB)

Li, H; Yang, D; Xiao, Z [Washington University School of Medicine, St. Louis, MO (United States); Driewer, J [University of Nebraska Medical Center, Omaha, NE (United States); Han, Z [Brigham and Womens Hospital and Harvard Medical School, Boston, MA (United States); Low, D [UCLA, Los Angeles, CA (United States)

2014-06-15

Purpose: Recent research has shown that KCl:Eu2+ has great potential for use in megavoltage radiation therapy dosimetry because this material exhibits excellent storage performance and is reusable due to strong radiation hardness. This work reports our attempts to fabricate 2D KCl:Eu2+ storage phosphor films (SPFs) using both a physical vapor deposition (PVD) method and a tape casting method. Methods: A thin layer of KCl:Eu2+ was deposited on a substrate of borosilicate glass (e.g., laboratory slides) with a PVD system. For tape casting, a homogenous suspension containing storage phosphor particles, liquid vehicle and polymer binder was formed and subsequently cast by doctor-blade onto a polyethylene terephthalate substrate to form a 150 μm thick SPF. Results: X ray diffraction analysis showed that a 10 μm thick PVD sample was composed of highly crystalline KCl. No additional phases were observed, suggesting that the europium activator had completed been incorporated into the KCl matrix. Photostimulated luminescence and photoluminescence spectra suggested that F (Cl−) centers were the electron storage centers post x ray irradiation and that Eu2+ cations acted as luminescence centers in the photostimulation process. The 150 μm thick casted KCl:Eu2+ SPF showed sub-millimeter spatial resolution. Monte Carlo simulations further demonstrated that the admixture of 20% KCl:Eu2+ and 80% low Z polymer binder exhibited almost no energy dependence in a 6 MV beam. KCl:Eu2+ pellet samples showed a large dynamic range from 0.01 cGy to 60 Gy dose-to-water, and saturated at approximately 500 Gy as a Result of its intrinsic high radiation hardness. Conclusions: This discovery research provides strong evidence that KCl:Eu2+ based SPF with associated readout apparatus could Result in a novel electronic film system that has all the desirable features associated with classic radiographic film and, importantly, water equivalence and the capability of permanent identification of

Enrichment of mushrooms: an interesting strategy for the acquisition of lithium.

Science.gov (United States)

de Assunção, Laélia Soares; da Luz, José Maria Rodrigues; da Silva, Marliane de Cássia Soares; Vieira, Patrícia Aparecida Fontes; Bazzolli, Denise Mara Soares; Vanetti, Maria Cristina Dantas; Kasuya, Maria Catarina Megumi

2012-09-15

The capability of Pleurotus ostreatus mushroom to accumulate lithium (Li) and the accessibility of this Li compared with lithium carbonate (Li(2)CO(3)), often used as psychiatric medicine, were investigated. Mushrooms were produced on a substrate-based on coffee husk, with different added concentrations of lithium chloride (LiCl). Biological efficiency (BE), the crude protein content, the concentration of Li and other elements present in mushrooms were determined. The sequential extraction and in vitro test were used to verify the accessibility and the degree of solubility of this element. Li concentration in mushrooms was directly influenced by increasing LiCl concentration in the substrate (Plithium can be an alternative source of Li, as well as being a food with high nutritional value. Copyright © 2012 Elsevier Ltd. All rights reserved.

Inhibition of isolated human myometrium contractility by minoxidil and reversal by glibenclamide.

Science.gov (United States)

Prabhakaran, S S; Dhanasekar, K R; Thomas, E; Jose, R; Peedicayil, J; Samuel, P

2010-03-01

This study investigated the ability of the antihypertensive drug minoxidil to inhibit potassium chloride (KCl)-induced contractility of the isolated human myometrium. Twelve strips of myometrium obtained from 12 patients who underwent hysterectomy were triggered to contract with 55 mM KCl before and after incubation with 3 concentrations (1, 3 and 10 microM) of minoxidil. The percent inhibition by minoxidil on the extent of contraction, and the area under the contractile curve of KCl-induced contraction of the myometrial strips was determined. Furthermore, the effect of 10 microM glibenclamide on the inhibition generated by 3 microM minoxidil on KCl-induced contractility was studied. It was found that minoxidil produced a concentration-dependent inhibition of KCl-induced contractility of the myometrium and that glibenclamide reversed this inhibitory effect. These results suggest that the inhibitory effect of minoxidil on isolated human myometrium contractility may prove useful in clinical conditions requiring relaxation of the myometrium. 2010 Prous Science, S.A.U. or its licensors. All rights reserved.

Use of alternative curing salts for processing salamis

Directory of Open Access Journals (Sweden)

Dong-Gyun Yim

2018-01-01

Full Text Available Objective This study was performed to determine effects of different curing salts on the quality of salamis and to assess feasibility of using NaCl-alternative salts. Methods Various types of curing salts (KCl or MgCl2 as well as NaCl (sun-dried or refined were incorporated for processing of salamis. The proximate composition, fatty acids, nucleotide-related compounds, and free amino acids of the salamis were analyzed during 40 days of ripening. Results The substitution of NaCl by KCl caused higher fat and ash content, but lower moisture content of the salami after 20 days of ripening (p<0.05. Compared with the sun-dried NaCl, use of KCl in salami also led to greater inosine 5′-monophosphate whereas refined NaCl had more inosine (p<0.05. KCl-added salami also had a higher C12:0, C17:1, and C20:0 than other types of salami (p<0.05. MgCl2-added salami had higher content of free amino acids compared to the other salamis (p<0.05. Conclusion Alternative curing salts such as KCl and MgCl2 could substitute NaCl in consideration of quality factor of a fermented meat product. Especially replacement of NaCl with KCl will be a suitable strategy for developing relatively low sodium salami products without compromising product quality.

Evolution of carboxymethyl cellulose layer morphology on hydrophobic mineral surfaces: variation of polymer concentration and ionic strength.

Science.gov (United States)

Beaussart, Audrey; Mierczynska-Vasilev, Agnieszka; Beattie, David A

2010-06-15

The adsorption of carboxymethyl cellulose (CMC) on the basal planes of talc and molybdenite has been studied using in situ atomic force microscope (AFM) imaging. These experiments were partnered with quantitative adsorption isotherm determinations on particulate samples. The isotherms revealed a clear increase of the CMC adsorbed amount upon increasing the solution ionic strength for adsorption on both minerals. In addition, the shapes of the isotherms changed in response to the change in the electrolyte concentration, with CMC on talc displaying stepped (10(-3) M KCl), Langmuir (10(-2) M KCl), then Freundlich isotherm shapes (10(-1) M KCl), and CMC on molybdenite displaying stepped (10(-3) M KCl), Freundlich (10(-2) M KCl), then Langmuir isotherm shapes (10(-1) M KCl). AFM imaging of the polymer layer on the mineral surfaces with varying solution conditions mirrored and confirmed the conclusions from the isotherms: as the polymer solution concentration increased, coverage on the basal plane increased; as the ionic strength increased, coverage on the basal plane increased and the morphology of the layer changed from isolated well-distributed polymer domains to extensive adsorption and formation of dense, uneven polymer domains/features. In addition, comparison of the talc and molybdenite datasets points toward the presence of different binding mechanisms for CMC adsorption on the talc and molybdenite basal plane surfaces. 2010 Elsevier Inc. All rights reserved.

Introducing a change in hospital policy using FMEA methodology as a tool to reduce patient hazards.

Science.gov (United States)

Ofek, Fanny; Magnezi, Racheli; Kurzweil, Yaffa; Gazit, Inbal; Berkovitch, Sofia; Tal, Orna

2016-01-01

Intravenous potassium chloride (IV KCl) solutions are widely used in hospitals for treatment of hypokalemia. As ampoules of concentrated KCL must be diluted before use, critical incidents have been associated with its preparation and administration. Currently, we have introduced ready-to-use diluted KCl infusion solutions to minimize the use of high-alert concentrated KCl. Since this process may be associated with considerable risks, we embraced a proactive hazard analysis as a tool to implement a change in high-alert drug usage in a hospital setting. Failure mode and effect analysis (FMEA) is a systematic tool to analyze and identify risks in system operations. We used FMEA to examine the hazards associated with the implementation of the ready-to-use solutions. A multidisciplinary team analyzed the risks by identifying failure modes, conducting a hazard analysis and calculating the criticality index (CI) for each failure mode. A 1-day survey was performed as an evaluation step after a trial run period of approximately 4 months. Six major possible risks were identified. The most severe risks were prioritized and specific recommendations were formulated. Out of 28 patients receiving IV KCl on the day of the survey, 22 received the ready-to-use solutions and 6 received the concentrated solutions as instructed. Only 1 patient received inappropriate ready-to-use KCl. Using the FMEA tool in our study has proven once again that by creating a gradient of severity of potential vulnerable elements, we are able to proactively promote safer and more efficient processes in health care systems. This article presents a utilization of this method for implementing a change in hospital policy regarding the routine use of IV KCl.

Strategies of Miniaturised Reference Electrodes Integrated in a Silicon Based “one chip” pH Sensor

OpenAIRE

Simonis, Anette; Lüth, Hans; Wang, Joseph; Schöning, J.

2003-01-01

Different types of Ag/AgCl reference electrodes have been realised by means of thin- and thick-film technique. For inner electrolyte, KCl-containing membranes have been deposited and different coatings have been used to protect the reference electrode from a fast leaching out of KCl. The stability of the potential of the reference electrodes without KClcontaining membranes in 3 M KCl was about 7 hours for thin-film electrodes and up to 90 hours for thick-film electrodes. The reference electro...

Teores foliares de nutrientes em mudas do abacaxizeiro ‘smooth cayenne’ em resposta à adubação Leaf nutrient contents on ´smooth cayenne´ planting material as response to fertilization

Directory of Open Access Journals (Sweden)

Ruimário Inácio Coelho

2010-12-01

Full Text Available Mudas do abacaxizeiro ‘Smooth Cayenne’ obtidas por seccionamento de caule foram submetidas à adubação foliar com soluções em diferentes concentrações de uréia, KCl e H3BO3, em pulverizações semanais, num total de vinte e seis para a uréia e o KCl e aplicações mensais num total de quatro, para o H3BO3. Todos os tratamentos foram iniciados na nona semana após o plantio das secções. O delineamento utilizado foi fatorial fracionado do tipo (1/553, com três tipos de adubo (uréia, KCl e H3BO3 e cinco concentrações num total de 25 tratamentos. Cada parcela constituiu-se de 50 secções. Os tratamentos consistiram nas combinações das seguintes concentrações em g L-1: 0; 2,5; 5; 7,5 e 10 para a uréia e o KCl, e 0; 0,5; 1; 1,5 e 2,0 de H3BO3. Análises das amostras de folhas “D” revelam efeitos da uréia e H3BO3 sobre os teores foliares de S, Cl e B e efeito do KCL sobre K e Cl foliar. A uréia não apresentou efeito sobre o teor de N foliar, porém influencia significativamente o conteúdo de N nas mudas.‘Smooth Cayenne’ planting material obtained through stem sectioning were trea-ted with foliar fertilization with different concentrations of urea, KCl, in weekly pulverizations, and H3BO4, totalizing twenty-six for urea and KCL pulverizations and four for H3BO3, which was applied monthly The treatments were began nine weeks after planting thestem sections. The experimental scheme was a fractionated factorial (1/55³ with three types of fertilizers (urea, KCl and H3BO3 and five concentrations in a total of 25 treatments. There were 50 sections per plot. Treatments were a combination of concentrations in g L-1: 0, 2.5, 5.0, 7.5 and 10 of urea and KCl, and 0, 0.5, 1.0, 1.5 and 2,0 of H3BO3. Sample analyses of ‘D’ leaves showed urea and H3BO3 effect on S, Cl and B leaf contents whereas KCL affected leaf K and Cl contents. Urea did not affect N leaf content, however it strongly influenced N content in planting material.

Crown Ether Complexes of Alkali-Metal Chlorides from SO2.

Science.gov (United States)

Reuter, Kirsten; Rudel, Stefan S; Buchner, Magnus R; Kraus, Florian; von Hänisch, Carsten

2017-07-18

The structures of alkali-metal chloride SO 2 solvates (Li-Cs) in conjunction with 12-crown-4 or 1,2-disila-12-crown-4 show strong discrepancies, despite the structural similarity of the ligands. Both types of crown ethers form 1:1 complexes with LiCl to give [Li(1,2-disila-12-crown-4)(SO 2 Cl)] (1) and [Li(12-crown-4)Cl]⋅4 SO 2 (2). However, 1,2-disila-12-crown-4 proved unable to coordinate cations too large for the cavity diameter, for example, by the formation of sandwich-type complexes. As a result, 12-crown-4 reacts exclusively with the heavier alkali-metal chlorides NaCl, KCl and RbCl. Compounds [Na(12-crown-4) 2 ]Cl⋅4 SO 2 (3) and [M(12-crown-4) 2 (SO 2 )]Cl⋅4 SO 2 (4: M=K; 5: M=Rb) all showed S-coordination to the chloride ions through four SO 2 molecules. Compounds 4 and 5 additionally exhibit the first crystallographically confirmed non-bridging O,O'-coordination mode of SO 2 . Unexpectedly, the disila-crown ether supports the dissolution of RbCl and CsCl in the solvent and gives the homoleptic SO 2 -solvated alkali-metal chlorides [MCl⋅3 SO 2 ] (6: M=Rb; 7: M=Cs), which incorporate bridging μ-O,O'-coordinating moieties and the unprecedented side-on O,O'-coordination mode. All compounds were characterised by single-crystal X-ray diffraction. The crown ether complexes were additionally studied by using NMR spectroscopy, and the presence of SO 2 at ambient temperature was revealed by IR spectroscopy of the neat compounds. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

L-alanine uptake in membrane vesicles from Mytilus edulis gills

International Nuclear Information System (INIS)

Pajor, A.M.; Wright, S.H.

1986-01-01

Previous studies have shown that gills from M. edulis can accumulate L-alanine from seawater by a saturable process specific for α-neutral amino acids. This uptake occurs against chemical gradients in excess of 10 6 to 1. To further characterize this uptake, membrane vesicles were prepared from M. edulis gill tissue by differential centrifugation. Enrichments of putative enzyme markers (relative to that in combined initial fractions) were as follows: γ-Glutamyltranspeptidase, 25-30x; Alkaline Phosphatase, 5-6x; K + -dependent para-Nitrophenyl Phosphatase, 3-5x; Succinate Dehydrogenase 0.1-0.2x. These results suggest that the preparation is enriched in plasma membranes, although histochemical studies will be needed to verify this. The time course of 14 C-L-alanine uptake in the presence of inwardly-directed Na + gradient showed a transient overshoot (3-5 fold) at 10 minutes which decreased to equilibrium after six hours. The size of the overshoot and early uptake rates depended on the size of the inwardly-directed Na + gradient. No overshoot was seen in the presence of inwardly-directed gradients of LiCl or choline-Cl, or with equilibrium concentrations NaCl or mannitol. A reduced overshoot was seen with a gradient of NaSCN. A small overshoot was seen with an inwardly-directed gradient of KCl. Transport of L-alanine included saturable and diffusive components. Uptake of 6 μM L-alanine was inhibited more than 80% by 100 μM α-zwitterionic amino acids (alanine, leucine, glycine); by 30 to 75% by proline, aspartate and lysine; and less than 20% by a β-amino acid, taurine. The results of these experiments agree with those from intact gill studies and support the hypothesis that L-alanine is transported into gill epithelial cells by a secondary active transport process involving Na +

Theoretical modeling of magnesium ion imprints in the Raman scattering of water.

Science.gov (United States)

Kapitán, Josef; Dracínský, Martin; Kaminský, Jakub; Benda, Ladislav; Bour, Petr

2010-03-18

Hydration envelopes of metallic ions significantly influence their chemical properties and biological functioning. Previous computational studies, nuclear magnetic resonance (NMR), and vibrational spectra indicated a strong affinity of the Mg(2+) cation to water. We find it interesting that, although monatomic ions do not vibrate themselves, they cause notable changes in the water Raman signal. Therefore, in this study, we used a combination of Raman spectroscopy and computer modeling to analyze the magnesium hydration shell and origin of the signal. In the measured spectra of several salts (LiCl, NaCl, KCl, MgCl(2), CaCl(2), MgBr(2), and MgI(2) water solutions), only the spectroscopic imprint of the hydrated Mg(2+) cation could clearly be identified as an exceptionally distinct peak at approximately 355 cm(-1). The assignment of this band to the Mg-O stretching motion could be confirmed on the basis of several models involving quantum chemical computations on metal/water clusters. Minor Raman spectral features could also be explained. Ab initio and Fourier transform (FT) techniques coupled with the Car-Parrinello molecular dynamics were adapted to provide the spectra from dynamical trajectories. The results suggest that even in concentrated solutions magnesium preferentially forms a [Mg(H(2)O)(6)](2+) complex of a nearly octahedral symmetry; nevertheless, the Raman signal is primarily associated with the relatively strong metal-H(2)O bond. Partially covalent character of the Mg-O bond was confirmed by a natural bond orbital analysis. Computations on hydrated chlorine anion did not provide a specific signal. The FT techniques gave good spectral profiles in the high-frequency region, whereas the lowest-wavenumber vibrations were better reproduced by the cluster models. Both dynamical and cluster computational models provided a useful link between spectral shapes and specific ion-water interactions.

Silicon electrodeposition from chloride-fluoride melts containing K2SiF6 and SiO2

Directory of Open Access Journals (Sweden)

Zhuk Sergey I.

2017-01-01

Full Text Available Silicon electrodeposition on glassy carbon from the KF-KCl-K2SiF6, KF-KCl-K2SiF6-KOH and KF-KCl-K2SiF6-SiO2 melts was studied by the cyclic voltammetry. Тhe electroreduction of Si(IV to metallic Si was observed as a single 4-electron wave under all considered conditions. The reactions of cathode reduction of silicon from fluoride and oxyfluoride complexes were suggested. It was shown that the process can be controlled by the preliminary transformation of SiO44- to SiF62- and SiOxFyz-. The influence of the current density on structure and morphology of silicon deposits obtained during galvanostatic electrolysis of the KF-KCl-K2SiF6-SiO2 melt was studied.

High temperature corrosion of thermally sprayed NiCr- and amorphous Fe-based coatings covered with a KCl-K{sub 2}SO{sub 4} salt

Energy Technology Data Exchange (ETDEWEB)

Varis, T.; Suhonen, T.; Tuurna, S.; Ruusuvuori, K.; Holmstroem, S.; Salonen, J. [VTT, Espoo (Finland); Bankiewicz, D.; Yrjas, P. [Aabo Akademi Univ., Turku (Finland)

2010-07-01

New process conditions due to the requirement of higher efficiency together with the use of high-chlorine and alkali containing fuels such as biomass and waste fuels for heat and electricity production will challenge the resistance and life of tube materials. In conventional materials the addition of alloying elements to increase the corrosion resistance in aggressive combustion conditions increases costs relatively rapidly. Thermally sprayed coating offer promising, effective, flexible and cost efficient solutions to fulfill the material needs for the future. Some heat exchanger design alteractions before global commercialization have to be overcome, though. High temperature corrosion in combustion plants can occur by a variety of mechanisms including passive scale degradation with subsequent rapid scaling, loss of adhesion and scale detachment, attack by melted or partly melted deposits via fluxing reactions and intergranular-/interlamellar corrosion. A generally accepted model of the ''active oxidation'' attributes the responsibility for inducing corrosion to chlorine. The active oxidation mechanism plays a key role in the thermally sprayed coatings due to their unique lamellar structure. In this study, the corrosion behaviour of NiCr (HVOF and Wire Arc), amorphous Fe-based, and Fe13Cr (Wire Arc) thermally sprayed coatings, were tested in the laboratory under simplified biomass combustion conditions. The tests were carried out by using a KCl-K{sub 2}SO{sub 4} salt mixture as a synthetic biomass ash, which was placed on the materials and then heat treated for one week (168h) at two different temperatures (550{sup 0}C and 600 C) and in two different gas atmospheres (air and air+30%H{sub 2}O). After the exposures, the metallographic cross sections of the coatings were studied with SEM/EDX analyzer. The results showed that the coatings behaved relatively well at the lower test temperature while critical corrosion through the lamella boundaries

K-capture by Al-Si based Additives in an Entrained Flow Reactor

DEFF Research Database (Denmark)

Wang, Guoliang; Jensen, Peter Arendt; Wu, Hao

2016-01-01

A water slurry, consisting of KCl and Al-Si based additives (kaolin and coal fly ash) was fed into an entrained flow reactor (EFR) to study the K-capturing reaction of the additives at suspension-fired conditions. Solid products collected from the reactor were analysed with respect to total...... of KCl to K-aluminosilicate decreased. When reaction temperature increased from 1100 °C to 1450 °C, the conversion of KCl does not change significantly, which differs from the trend observed in fixed-bed reactor....

Experimental study on soluble chemical transfer to surface runoff from soil.

Science.gov (United States)

Tong, Juxiu; Yang, Jinzhong; Hu, Bill X; Sun, Huaiwei

2016-10-01

Prevention of chemical transfer from soil to surface runoff, under condition of irrigation and subsurface drainage, would improve surface water quality. In this paper, a series of laboratory experiments were conducted to assess the effects of various soil and hydraulic factors on chemical transfer from soil to surface runoff. The factors include maximum depth of ponding water on soil surface, initial volumetric water content of soil, depth of soil with low porosity, type or texture of soil and condition of drainage. In the experiments, two soils, sand and loam, mixed with different quantities of soluble KCl were filled in the sandboxes and prepared under different initial saturated conditions. Simulated rainfall induced surface runoff are operated in the soils, and various ponding water depths on soil surface are simulated. Flow rates and KCl concentration of surface runoff are measured during the experiments. The following conclusions are made from the study results: (1) KCl concentration in surface runoff water would decrease with the increase of the maximum depth of ponding water on soil surface; (2) KCl concentration in surface runoff water would increase with the increase of initial volumetric water content in the soil; (3) smaller depth of soil with less porosity or deeper depth of soil with larger porosity leads to less KCl transfer to surface runoff; (4) the soil with finer texture, such as loam, could keep more fertilizer in soil, which will result in more KCl concentration in surface runoff; and (5) good subsurface drainage condition will increase the infiltration and drainage rates during rainfall event and will decrease KCl concentration in surface runoff. Therefore, it is necessary to reuse drained fertile water effectively during rainfall, without polluting groundwater. These study results should be considered in agriculture management to reduce soluble chemical transfer from soil to surface runoff for reducing non-point sources pollution.