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Sample records for aluminum chloride solution

  1. Some physicochemical properties of aluminum and iron chloride solutions

    NASA Astrophysics Data System (ADS)

    Balmaev, B. G.; Tuzhilin, A. S.; Shebalkova, A. Yu.; Rozhkov, D. Yu.

    2016-11-01

    Some physicochemical properties of aluminum and iron chloride solutions are considered. The density and viscosity of aluminum and iron chlorides are plotted as functions of the FeCl3/(FeCl3 + AlCl3) ratio and temperature, and pH of aluminum hydroxochlorides is plotted as a function of the Al2O3 content in a solution and its basicity (ratio of contents Al/Cl). The joint solubility of aluminum hydroxochloride and sodium chloride in water has been analyzed.

  2. An XAFS study of nickel chloride in the ionic liquid 1-ethyl-3-methyl imidazolium chloride/ aluminum chloride

    SciTech Connect

    D Roeper; G Cheek; K Pandya; W OGrady

    2011-12-31

    Nickel chloride was studied with cyclic voltammetry and X-ray absorption spectroscopy in acidic and basic aluminum chloride/1-ethyl-3-methyl imidazolium chloride (EMIC) ionic liquids. Acidic melts display metal stripping peaks which are not observed in the basic melt. EXAFS analysis shows that the nickel is tetrahedrally coordinated with chloride ions in the basic solution. In the acidic solution the nickel is coordinated by six chloride ions that are also associated with aluminum ions.

  3. Effects of applied potential on the stress corrosion cracking behavior of 7003 aluminum alloy in acid and alkaline chloride solutions

    NASA Astrophysics Data System (ADS)

    Zhang, Xiao-yan; Song, Ren-guo; Sun, Bin; Lu, Hai; Wang, Chao

    2016-07-01

    Potentiodynamic polarization tests and slow strain rate test (SSRT) in combination with fracture morphology observations were conducted to investigate the stress corrosion cracking (SCC) behavior of 7003 aluminum alloy (AA7003) in acid and alkaline chloride solutions under various applied potentials ( E a). The results show that AA7003 is to a certain extent susceptible to SCC via anodic dissolution (AD) at open-circuit potential (OCP) and is highly susceptible to hydrogen embrittlement (HE) at high negative E a in the solutions with pH levels of 4 and 11. The susceptibility increases with negative shift in the potential when E a is less than -1000 mV vs. SCE. However, the susceptibility distinctly decreases because of the inhibition of AD when E a is equal to -1000 mV vs. SCE. In addition, the SCC susceptibility of AA7003 in the acid chloride solution is higher than that in the alkaline solution at each potential. Moreover, the effect of hydrogen on SCC increases with increasing hydrogen ion concentration.

  4. Pain and swelling after periapical surgery related to the hemostatic agent used: Anesthetic solution with vasoconstrictor or aluminum chloride

    PubMed Central

    Maestre-Ferrín, Laura; Peñarrocha-Oltra, David; Gay-Escoda, Cosme; von-Arx, Tomas; Peñarrocha-Diago, Miguel

    2012-01-01

    Objective: To assess pain and swelling in the first 7 days after periapical surgery and their relationship with the agent used for bleeding control. Study Design: A prospective study was conducted between October 2006 and March 2009. Patients subjected to root surgery, who completed the questionnaire and who consented to the postoperative instructions were included in the study. The subjects were divided into two groups according to the hemostatic agent used: A) gauze impregnated with anesthetic solution with vasoconstrictor; or B) aluminum chloride. The patients were administered a questionnaire, and were asked to record the severity of their pain and swelling on a plain horizontal visual analog scale (VAS). Data were recorded by the patients on the first 7 postoperative days. In addition, the patients were asked to record analgesic consumption. Results: A total of 76 questionnaires (34 in group A and 42 in group B) were taken to be correctly completed. Pain was reported to be most intense two hours after surgery. At this point 52.6% of the patients had no pain. Seventy-five percent of the patients consumed analgesics in the first 24 hours. There were no significant differences between the two groups in terms of the intensity of pain or in the consumption of analgesics. Swelling reached its maximum peak on the second day; at this point, 60.6% of the patients suffered mild or moderate swelling. The Expasyl™ group showed significantly greater swelling than the gauzes group. Conclusion: The type of hemostatic agent used did not influence either the degree of pain or the need for analgesia among the patients in this study. However, the patients belonging to the Expasyl™ group suffered greater swelling than the patients treated with gauzes impregnated with anesthetic solution with vasoconstrictor. Key words:Hemostasis, periradicular surgery, aluminum chloride, pain, swelling. PMID:22322510

  5. Production of anhydrous aluminum chloride composition

    DOEpatents

    Vandergrift, G.F. III; Krumpelt, M.; Horwitz, E.P.

    1981-10-08

    A process is described for producing an anhydrous aluminum chloride composition from a water-based aluminous material such as a slurry of aluminum hydroxide in a multistage extraction process in which the aluminum ion is first extracted into an organic liquid containing an acidic extractant and then extracted from the organic phase into an alkali metal chloride or chlorides to form a melt containing a mixture of chlorides of alkali metal and aluminum. In the process, the organic liquid may be recycled. In addition, the process advantageously includes an electrolysis cell for producing metallic aluminum and the alkali metal chloride or chlorides may be recycled for extraction of the aluminum from the organic phase.

  6. Fabrication and icing property of superhydrophilic and superhydrophobic aluminum surfaces derived from anodizing aluminum foil in a sodium chloride aqueous solution

    NASA Astrophysics Data System (ADS)

    Song, Meirong; Liu, Yuru; Cui, Shumin; Liu, Long; Yang, Min

    2013-10-01

    An aluminum foil with a rough surface was first prepared by anodic treatment in a neutral aqueous solution with the help of pitting corrosion of chlorides. First, the hydrophobic Al surface (contact angle around 79°) became superhydrophilic (contact angle smaller than 5°) after the anodizing process. Secondly, the superhydrophilic Al surface became superhydrophobic (contact angle larger than 150°) after being modified by oleic acid. Finally, the icing property of superhydrophilic, untreated, and superhydrophobic Al foils were investigated in a refrigerated cabinet at -12 °C. The mean total times to freeze a water droplet (6 μL) on the three foils were 17 s, 158 s and 1604 s, respectively. Thus, the superhydrophilic surface accelerates the icing process, while the superhydrophobic surface delays the process. The main reason for this transition might mainly result from the difference of the contact area of the water droplet with Al substrate: the increase in contact area with Al substrate will accelerate the heat conduct process, as well as the icing process; the decrease in contact area with Al substrate will delay the heat conduct process, as well as the icing process. Compared to the untreated Al foil, the contact area of the water droplet with the Al substrate was higher on superhydrophilic surface and smaller on the superhydrophobic surface, which led to the difference of the heat transfer time as well as the icing time.

  7. An XAFS Study of Tantalum Chloride in the Ionic Liquid 1-ethyl-3-methyl Imidazolium Chloride/ aluminum Chloride

    SciTech Connect

    D Roeper; K Pandya; G Cheek; W OGrady

    2011-12-31

    Tantalum chloride was studied with extended X-ray absorption fine structure spectroscopy (XAFS) in acidic and basic aluminum chloride/1-ethyl-3-methyl imidazolium chloride ionic liquids (ILs). Anhydrous Ta2Cl10 is more soluble in the basic solution than in the acidic solution and the X-ray absorption data shows that the coordination shell of chlorides around the tantalum is larger in the basic solution. In the acidic solution, tantalum has five chlorides in its coordination shell while in the basic solution; the tantalum is coordinated by seven chlorides. This indicates that the Lewis acidity of the tantalum chloride causes the Ta to coordinate differently in the acidic and the basic solutions.

  8. A Green Alternative to Aluminum Chloride Alkylation of Xylene

    ERIC Educational Resources Information Center

    Sereda, Grigoriy A.; Rajpara, Vikul B.

    2007-01-01

    An acutely less toxic 2-bromobutane is used to develop a simple graphite-promoted procedure of alkylation of p-xylene. It is further demonstrated that aluminum chloride is not required, the need for aqueous workup is eliminated, waste solutions are not produced and the multiple use of the catalyst is allowed.

  9. Inhibition of corrosion of Al 6061, aluminum, and an aluminum-copper alloy in chloride-free aqueous media. Part 2: Behavior in basic solutions

    SciTech Connect

    Al-Kharafi, F.M.; Badawy, W.A.

    1998-05-01

    Electrochemical characteristics of Al 6061 (UNS A96061), Al and an Al-Cu alloy were investigated in aqueous solutions. Inhibition of the corrosion processes in basic solutions was studied using electrochemical impedance spectroscopy (EIS) and polarization techniques. Among a series of inhibitors, molybdate (MoO{sub 4}{sup 2{minus}}) and dichromates (Cr{sub 2}O{sub 7}{sup 2{minus}}) were found effective in passivating the metal or alloy surface. The high inhibition action of Cr{sub 2}O{sub 7}{sup 2{minus}} was traced and discussed. X-ray photoelectron spectroscopy (XPS) of the different electrode materials revealed the presence of Cu peaks on the Al-Cu alloy surface. Immersion of the different electrodes in basic solutions containing the same concentration of Cr{sub 2}O{sub 7}{sup 2{minus}}, MoO{sub 4}{sup 2{minus}}, and sulfate (SO{sub 4}{sup 2{minus}}) anions did not show characteristic peaks of Cr, Mo, or S, which meant the surface layer consisted mainly of aluminum oxide (Al{sub 2}O{sub 3}). Depth profiling experiments up to 6.0-nm thickness showed the Cu peaks of the Al-Cu alloy appeared after etching and that Mo was incorporated in the surface film. The presence of Cu on the Al-Cu surface initiated flawed regions, identified by scanning electron microscopy, which were responsible for increased corrosion rates of this alloy. Effectiveness of the dichromate as a corrosion inhibitor for these materials resulted from its powerful oxidizing properties, which led to formation of a stable passive film.

  10. The Structure of Nickel Chloride in the Ionic Liquid 1-Ethyl-3-methyl Imidazolium Chloride/Aluminum Chloride: X-ray Absorption Spectroscopy

    SciTech Connect

    D Roeper; K Pandya; G Cheek; W OGrady

    2011-12-31

    The structure of anhydrous nickel chloride in the ionic liquid 1-ethyl-3-methyl imidazolium chloride and aluminum chloride has been investigated with extended X-ray absorption fine structure (EXAFS) in both Lewis acid and Lewis base solutions. The EXAFS data of NiCl{sub 2} {center_dot} 6H{sub 2}O crystals were also recorded and analyzed to demonstrate the difference file technique. The difference file technique is used to obtain the structural information for the very closely spaced coordination shells of chloride and oxygen in NiCl{sub 2} {center_dot} 6H{sub 2}O and they are found to agree very closely with the X-ray diffraction data. The difference file technique is then used to analyze the nickel chloride in the ionic liquid solutions. Even though anhydrous NiCl{sub 2} is more soluble in the basic solution than in the acidic solution, the EXAFS data show a single coordination of four chlorides in a tetrahedron around the nickel atom in the basic solution. In a weak acid solution, there are six chlorides in a single octahedral coordination shell around the nickel. However, in a strong acid solution, in addition to the octahedral chloride-coordination shell, there is a second coordination shell of eight aluminum atoms in the form of a simple cube.

  11. Aluminum Chloride Hexahydrate in a Salicylic Acid Gel

    PubMed Central

    Valins, Whitney

    2009-01-01

    Hyperhidrosis is a common dermatological condition that has a tremendous impact on the quality of life of affected patients. Aluminum chloride hexahydrate is considered first-line therapy for patients with mild-to-moderate hyperhidrosis. This treatment has been proven to be effective in the treatment of hyperhidrosis; however, its use has been limited by significant irritation. In many patients, the irritant dermatitis is so severe that, despite clinical efficacy, this therapy must be discontinued. There are many topical aluminum chloride therapies available. Observations from a busy hyperhidrosis practice revealed decreased irritation and increased efficacy with a novel therapy that combines 15% aluminum chloride hexahydrate with 2% salicylic acid in a gel base. This combination of 15% aluminum chloride hexahydrate with 2% salicylic acid offers patients who have failed aluminum chloride hexahydrate in the past excellent efficacy with minimal irritation. We report seven cases of patients with a history of severe irritation from aluminum chloride who maintained excellent results with this new topical without any significant irritation. PMID:20729946

  12. REMOVAL OF CHLORIDE FROM AQUEOUS SOLUTIONS

    DOEpatents

    Schulz, W.W.

    1959-08-01

    The removal of chlorides from aqueons solutions is described. The process involves contacting the aqueous chloride containing solution with a benzene solution about 0.005 M in phenyl mercuric acetate whereby the chloride anions are taken up by the organic phase and separating the organic phase from the aqueous solutions.

  13. Structure of complexes between aluminum chloride and other chlorides, 2: Alkali-(chloroaluminates). Gaseous complexes

    NASA Technical Reports Server (NTRS)

    Hargittai, M.

    1980-01-01

    The structural chemistry of complexes between aluminum chloride and other metal chlorides is important both for practice and theory. Condensed-phase as well as vapor-phase complexes are of interest. Structural information on such complexes is reviewed. The first emphasis is given to the molten state because of its practical importance. Aluminum chloride forms volatile complexes with other metal chlorides and these vapor-phase complexes are dealt with in the second part. Finally, the variations in molecular shape and geometrical parameters are summarized.

  14. Corrosion-electrochemical properties of the anodic oxide films formed on aluminum in a chloride-nitrate melt in a 0.5 M Aqueous NaCl solution

    NASA Astrophysics Data System (ADS)

    Elshina, L. A.; Malkov, V. B.; Kudyakov, V. Ya.; Gnedenkov, S. V.; Sinebryukhov, S. L.; Egorkin, V. S.; Mashtalyar, D. V.

    2014-02-01

    The corrosion-electrochemical behavior of aluminum is studied in a chloride-nitrate melt containing 50 wt % eutectic mixture of cesium and sodium chlorides and 50 wt % sodium nitrate in the temperature range 790-900 K in an argon atmosphere.

  15. Production of anhydrous aluminum chloride composition and process for electrolysis thereof

    DOEpatents

    Vandegrift, George F.; Krumpelt, Michael; Horwitz, E. Philip

    1983-01-01

    A process for producing an anhydrous aluminum chloride composition from a water-based aluminous material such as a slurry of aluminum hydroxide in a multistage extraction process in which the aluminum ion is first extracted into an organic liquid containing an acidic extractant and then extracted from the organic phase into an alkali metal chloride or chlorides to form a melt containing a mixture of chlorides of alkali metal and aluminum. In the process, the organic liquid may be recycled. In addition, the process advantageously includes an electrolysis cell for producing metallic aluminum and the alkali metal chloride or chlorides may be recycled for extraction of the aluminum from the organic phase.

  16. 40 CFR 415.10 - Applicability; description of the aluminum chloride production subcategory.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... aluminum chloride production subcategory. 415.10 Section 415.10 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Aluminum Chloride Production Subcategory § 415.10 Applicability; description of the aluminum chloride production subcategory. The provisions of this subpart are applicable to discharges...

  17. 40 CFR 415.10 - Applicability; description of the aluminum chloride production subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... aluminum chloride production subcategory. 415.10 Section 415.10 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Aluminum Chloride Production Subcategory § 415.10 Applicability; description of the aluminum chloride production subcategory. The provisions of this subpart are applicable to discharges...

  18. 40 CFR 415.10 - Applicability; description of the aluminum chloride production subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... aluminum chloride production subcategory. 415.10 Section 415.10 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Aluminum Chloride Production Subcategory § 415.10 Applicability; description of the aluminum chloride production subcategory. The provisions of this subpart are applicable to discharges...

  19. 40 CFR 415.10 - Applicability; description of the aluminum chloride production subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... aluminum chloride production subcategory. 415.10 Section 415.10 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Aluminum Chloride Production Subcategory § 415.10 Applicability; description of the aluminum chloride production subcategory. The provisions of this subpart are applicable to discharges...

  20. 40 CFR 415.10 - Applicability; description of the aluminum chloride production subcategory.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... aluminum chloride production subcategory. 415.10 Section 415.10 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Aluminum Chloride Production Subcategory § 415.10 Applicability; description of the aluminum chloride production subcategory. The provisions of this subpart are applicable to discharges...

  1. An XAFS Study of Niobium chloride in the ionic liquid 1-ethyl-3-methyl imidazolium chloride/ aluminum chloride

    SciTech Connect

    D Roeper; K Pandya; G Cheek; W OGrady

    2011-12-31

    Niobium chloride was studied with extended X-ray absorption fine structure spectroscopy (EXAFS) in acidic and basic aluminum chloride/1-ethyl-3-methyl imidazolium chloride (EMIC) ionic liquids. Although anhydrous Nb2Cl10 is more soluble in the basic melt than in the acidic melt, the EXAFS data shows that the coordination shell around the niobium does not change in the different ionic liquids. Both the acidic and basic melts show a coordination of five chlorides in the first shell. This indicates that in this series of ionic liquids, the Nb2Cl10 breaks up into two NbCl5 entities in both the acidic and the basic melts.

  2. Densities, Electrical Conductivities, Viscosities and Phase Equilibria of 1,3-Dialkylimidazolium Chloride - Aluminum Chloride Binary and Ternary Melts.

    DTIC Science & Technology

    1982-07-01

    FRANK J. SELLER RESEARCH LABORATORY FJSRL-TR-82-0006 JULY 1982 DENSITIES, ELEC’TRICAL CONDUCTIVITIES, VISCOSITIES AND PHASE EQUILIBRIA OF 1,3...Conductivities, Viscosities and Phase Equilibria of 1,3- Interim 6/81-7/82 Dialkylimidazolium Chloride-Aluminum Chloride 6. PERFORMING ORG. REPORT NUMBER...Entered) FJSRL-TR-82-0006 DENSITIES, ELECTRICAL CONDUCTIVITIES, VISCOSITIES AND PHASE EQUILIBRIA OF 1,3-DIALKYLIMIDAZOLIUM CHLORIDE- ALUMINUM CHLORIDE

  3. Solution Potentials Indicate Aluminum-Alloy Tempers

    NASA Technical Reports Server (NTRS)

    Danford, M. D.

    1985-01-01

    Report discusses use of solution potential as measure of temper of aluminum alloys. Technique based on fact that different tempers or heat treatments exhibit different solution potentials as function of aging time.

  4. XAFS Studies of Ni Ta and Nb Chlorides in the Ionic Liquid 1-Ethyl-3-Methyl Imidazolium Chloride / Aluminum Chloride

    SciTech Connect

    W OGrady; D Roeper; K Pandya; G Cheek

    2011-12-31

    The structures of anhydrous nickel, niobium, and tantalum chlorides have been investigated in situ in acidic and basic ionic liquids (ILs) of 1-methyl-3-ethylimidazolium chloride (EMIC)/AlCl{sub 3} with X-ray absorption spectroscopy (XAS). The coordination of NiCl{sub 2} changes from tetrahedral in basic solution to octahedral in acidic solution. The NiCl{sub 2} is a strong Lewis acid in that it can induce the AlCl{sub 3} to share its chlorides in the highly acidic IL, forming a structure with six near Cl{sup -} ions and eight further distant Al ions which share the chloride ions surrounding the Ni{sup 2+}. When Nb{sub 2}Cl{sub 10}, a dimer, is added to the acidic or basic solution, the dimer breaks apart and forms two species. In the acid solution, two trigonal bipyramids are formed with five equal chloride distances, while in the basic solution, a square pyramid with four chlorides forming a square base and one shorter axial chloride bond. Ta{sub 2}Cl{sub 10} is also a dimer and divides into half in the acidic solution and forms two trigonal bipyramids. In the basic solution, the dimer breaks apart but the species formed is sufficiently acidic that it attracts two additional chloride ions and forms a seven coordinated tantalum species.

  5. Xylan hydrolysis in zinc chloride solution

    SciTech Connect

    Cao, N.J.; Xu, Q.; Chen, L.F

    1995-12-31

    Xylan is the major component of hemicellulose, which consists of up to one-third of the lignocellulosic biomass. When the zinc chloride solution was used as a pretreatment agent to facilitate cellulose hydrolysis, hemicellulose was hydrolyzed during the pretreatment stage. In this study, xylan was used as a model to study the hydrolysis of hemicellulose in zinc chloride solution. The degradation of xylose that is released from xylan was reduced by the formation of zinc-xylose complex. The xylose yield was > 90% (w/w) at 70{degrees}C. The yield and rate of hydrolysis were a function of temperature and the concentration of zinc chloride. The ratio of zinc chloride can be decreased from 9 to 1.3 (w/w). At this ratio, 76% of xylose yield was obtained. When wheat straw was pretreated with a concentrated zinc chloride solution, the hemicellulose hydrolysate contained only xylose and trace amounts of arabinose and oligosaccharides. With this approach, the hemicellulose hydrolysate can be separated from cellulose residue, which would be hydrolyzed subsequently to glucose by acid or enzymes to produce glucose. This production scheme provided a method to produce glucose and xylose in different streams, which can be fermented in separated fermenters.

  6. Hydrolysis of diethyl aluminum chloride on an inorganic filler surface

    SciTech Connect

    Gorelik, V.M.; Shesternina, L.A.; Emel'yanova, A.D.; Borisova, L.F.; Fushman, E.A.; Berner, V.S.; Korneev, N.N.

    1986-04-20

    There has been increased interest recently in the use of natural aluminosilicates as carriers of organometallic catalysts for the polymerization of alkenes. Polymerization in catalyst systems fixed on kaolin, tufa, etc., is aimed at obtaining highly filled polymers. Since complex organometallic catalysts are highly sensitive to proton donors, water in particular, aluminosilicate carriers are usually heat-treated before they come into contact with the catalyst's components. This paper reports an investigation of the interaction of organoaluminum compounds with the functional groups on a kaolin surface. They determined some quantitative characteristics of the hydrolysis reaction of diethyl aluminum chloride and suggest that organoaluminum compounds are also consumed in reactions with siloxane groups on the surface.

  7. Solid propellant exhausted aluminum oxide and hydrogen chloride - Environmental considerations

    NASA Technical Reports Server (NTRS)

    Cofer, W. R., III; Winstead, E. L.; Purgold, G. C.; Edahl, R. A.

    1993-01-01

    Measurements of gaseous hydrogen chloride (HCl) and particulate aluminum oxide (Al2O3) were made during penetrations of five Space Shuttle exhaust clouds and one static ground test firing of a shuttle booster. Instrumented aircraft were used to penetrate exhaust clouds and to measure and/or collect samples of exhaust for subsequent analyses. The focus was on the primary solid rocket motor exhaust products, HCl and Al2O3, from the Space Shuttle's solid boosters. Time-dependent behavior of HCl was determined for the exhaust clouds. Composition, morphology, surface chemistry, and particle size distributions were determined for the exhausted Al2O3. Results determined for the exhaust cloud from the static test firing were complicated by having large amounts of entrained alkaline ground debris (soil) in the lofted cloud. The entrained debris may have contributed to neutralization of in-cloud HCl.

  8. Chloride removal from recycled cooling water using ultra-high lime with aluminum process.

    PubMed

    Abdel-Wahab, Ahmed; Batchelor, Bill

    2002-01-01

    Chloride is a deleterious ionic species in cooling water systems because it promotes corrosion, and most of the scale and corrosion inhibitors are sensitive to chloride concentration in the water. Chloride can be removed from cooling water by precipitation as calcium chloroaluminate [Ca4Al2Cl2(OH)12]. A set of equilibrium experiments and one kinetic experiment were conducted to evaluate chloride removal using the ultra-high lime with aluminum (UHLA) process and to characterize the equilibrium conditions of calcium chloroaluminate precipitation. A total of 48 batch-equilibrium experiments were conducted on a 30 mM NaCl solution over a range of values for lime dose (0 to 200 mM) and sodium aluminate dose (0 to 100 mM). Experimental results showed that the UHLA process can remove chloride and that the formation of a calcium chloroaluminate solid phase is a reasonable mechanism that is able to adequately describe experimental results. An average value of the ion activity product of 10(-94.75) was obtained and can be used as an estimate of the solubility product for Ca4Al2Cl2(OH)12.

  9. Anodizing And Sealing Aluminum In Nonchromated Solutions

    NASA Technical Reports Server (NTRS)

    Emmons, John R.; Kallenborn, Kelli J.

    1995-01-01

    Improved process for anodizing and sealing aluminum involves use of 5 volume percent sulfuric acid in water as anodizing solution, and 1.5 to 2.0 volume percent nickel acetate in water as sealing solution. Replaces process in which sulfuric acid used at concentrations of 10 to 20 percent. Improved process yields thinner coats offering resistance to corrosion, fatigue life, and alloy-to-alloy consistency equal to or superior to those of anodized coats produced with chromated solutions.

  10. Elastin Calcification and its Prevention with Aluminum Chloride Pretreatment

    PubMed Central

    Vyavahare, Narendra; Ogle, Matthew; Schoen, Frederick J.; Levy, Robert J.

    1999-01-01

    Elastin, an abundant structural protein present in the arterial wall, is prone to calcification in a number of disease processes including porcine bioprosthetic heart valve calcification and atherosclerosis. The mechanisms of elastin calcification are not completely elucidated. In the present work, we demonstrated calcification of purified elastin in rat subdermal implants (Ca2+ = 89.73 ± 9.84 μg/mg after 21 days versus control, unimplanted Ca2+ = 0.16 ± 0.04 μg/mg). X-ray diffraction analysis along with resolution enhanced FTIR spectroscopy demonstrated the mineral phase to be a poorly crystalline hydroxyapatite. We investigated the time course of calcification, the effect of glutaraldehyde crosslinking on calcification, and mechanisms of inhibition of elastin calcification by pretreatment with aluminum chloride (AlCl3). Glutaraldehyde pretreatment did not affect calcification (Ca2+ = 89.06 ± 17.93 μg/mg for glutaraldehyde crosslinked elastin versus Ca2+ = 89.73 ± 9.84 μg/mg for uncrosslinked elastin). This may be explained by radioactive (3H) glutaraldehyde studies showing very low reactivity between glutaraldehyde and elastin. Our results further demonstrated that AlCl3 pretreatment of elastin led to complete inhibition of elastin calcification using 21-day rat subdermal implants, irrespective of glutaraldehyde crosslinking (Ca2+ = 0.73–2.15 μg/mg for AlCl3 pretreated elastin versus 89.73 ± 9.84 for untreated elastin). The AlCl3 pretreatment caused irreversible binding of aluminum ions to elastin, as assessed by atomic emission spectroscopy. Moreover, aluminum ion binding altered the spatial configuration of elastin as shown by circular dichroism (CD), Fourier transform infrared (FTIR), and 13C nuclear magnetic resonance (NMR) spectroscopy studies, suggesting a net structural change including a reduction in the extent of β sheet structures and an increase in coil-turn conformations. Thus, it is concluded that purified elastin calcifies in rat

  11. Trivalent Chromium Solutions for Sealing Anodized Aluminum

    DTIC Science & Technology

    1994-12-20

    the comparatively innocuous trivalent form before acid , chromic acid , oxalic acid , sulfophthalic acid , boric disposal. This method is expensive and...or had only faint anodized aluminum substrates by immersion in a mildly traces of corrosion . All 7075-T6 panels provided with acid solution containing...alloy panels wereP 10 anodized in 15% (weight) sulfuric acid solution for 30 To produce improved corrosion resistance on anod- minutes at 21 C. at 18

  12. Hydrolysis of ferric chloride in solution

    SciTech Connect

    Lussiez, G.; Beckstead, L.

    1996-11-01

    The Detox{trademark} process uses concentrated ferric chloride and small amounts of catalysts to oxidize organic compounds. It is under consideration for oxidizing transuranic organic wastes. Although the solution is reused extensively, at some point it will reach the acceptable limit of radioactivity or maximum solubility of the radioisotopes. This solution could be cemented, but the volume would be increased substantially because of the poor compatibility of chlorides and cement. A process has been developed that recovers the chloride ions as HCl and either minimizes the volume of radioactive waste or permits recycling of the radioactive chlorides. The process involves a two-step hydrolysis at atmospheric pressure, or preferably under a slight vacuum, and relatively low temperature, about 200{degrees}C. During the first step of the process, hydrolysis occurs according to the reaction below: FeCl{sub 3 liquid} + H{sub 2}O {r_arrow} FeOCl{sub solid} + 2 HCl{sub gas} During the second step, the hot, solid, iron oxychloride is sprayed with water or placed in contact with steam, and hydrolysis proceeds to the iron oxide according to the following reaction: 2 FeOCl{sub solid} + H{sub 2}O {r_arrow} Fe{sub 2}O{sub 3 solid} + 2 HCl{sub gas}. The iron oxide, which contains radioisotopes, can then be disposed of by cementation or encapsulation. Alternately, these chlorides can be washed off of the solids and can then either be recycled or disposed of in some other way.

  13. REMOVAL OF CHLORIDE FROM AQUEOUS SOLUTIONS

    DOEpatents

    Hyman, M.L.; Savolainen, J.E.

    1960-01-01

    A method is given for dissolving reactor fuel elements in which the uranium is associated with a relatively inert chromium-containing alloy such as stainless steel. An aqueous mixture of acids comprising 2 to 2.5 molar hydrochloric acid and 4 to 8 molar nitric acid is employed in dissolving the fuel element. In order io reduce corrosion in subsequent processing of the resulting solution, chloride values are removed from the solution by contacting it with concentrated nitric acid at an elevated temperature.

  14. Properties and coagulation performance of coagulant poly-aluminum-ferric-silicate-chloride in water and wastewater treatment.

    PubMed

    Gao, Bao-yu; Yue, Qin-yan; Wang, Bing-jian

    2006-01-01

    An efficient inorganic polymer coagulant, poly-aluminum-ferric-silicate-chloride (PAFSC), was developed using two approaches: (i) hydroxylation of the mixture of AlCl3, FeCl3 and fresh polysilicic acid in different Al/Fe/Si molar ratios to obtain PAFSCc and (ii) hydroxylated poly-aluminum-iron-chloride (PAFC) combined with aged polysilicic acid in different Al/Fe/Si ratios to produce PAFSCm. The properties of PAFSC in comparison with polyaluminum silicate chloride (PASC) and polyferric silicate chloride (PAFC) were characterized by various experimental methods. The effect of Al/Fe/Si molar ratio on the hydrolysis-polymerization process of Al (III) and Fe (III) in PAFSC solutions was examined by pH titration, and the effect of Al/Fe/Si molar ratio on electrokinetic mobility of PAFSC was studied by Zeta potential measurement. The laboratory experiments were performed to evaluate the PAFSC in comparison with polyaluminum chloride (PAC) for the coagulation of synthetic water samples, actual surface water and wastewater. The results show that interactions exist among aluminum species, ferric species and polysilicic acid, and the Al/Fe/Si molar ratio affects the Zeta potential of the hydrolyzate and the coagulating performance. PAFSC achieved a better water treatment result than PAC. At the same basicity (B) value and Al/Fe/Si ratio, PAFSCc has better coagulation performance than PAFSCm. PAFSC is a new type and high efficiency composite inorganic polymer coagulant.

  15. The Toxicity of Aluminum Chloride on Kidney of Rats.

    PubMed

    Liu, Jianyu; Wang, Qin; Sun, Xudong; Yang, Xu; Zhuang, Cuicui; Xu, Feibo; Cao, Zheng; Li, Yanfei

    2016-10-01

    This study investigated the toxicity of aluminum chloride (AlCl3) exposure in the rat kidney. Forty male Wistar rats (5 weeks old), weighing 110-120 g, were randomly divided into four groups: control group (CG, 0 g/L AlCl3), low dose group (LG, 0.4 g/L AlCl3), mid dose group (MG, 0.8 g/L AlCl3), and high dose group (HG, 1.6 g/L AlCl3). Rats were administered AlCl3 in their drinking water for 120 days. A variety of measurements were taken including superoxide dismutase (SOD) and glutathione peroxidase (GSH-PX) activities, malondialdehyde (MDA) concentration in the kidney and blood urea nitrogen (BUN), and cystatin C (Cys-C) concentrations in the serum. In addition, Al and β2-microglobulin (β2-MG) concentrations and the activity of N-acetyl-β-D-glucosaminidase (NAG) in the urine were determined. The results showed that in the AlCl3-treated groups SOD and GSH-PX activities were decreased, while NAG activity and Al, MDA, BUN, Cys-C, and β2-MG concentrations were increased, compared with the CG. This study indicates that AlCl3 exposure induces oxidative stress and suppresses kidney function.

  16. Infrared spectra of cesium chloride aqueous solutions

    NASA Astrophysics Data System (ADS)

    Max, Jean-Joseph; Chapados, Camille

    2000-10-01

    The aqueous solutions of CsCl were studied at room temperature by infrared (IR) spectroscopy in the entire solubility range, 0-1200 g/L, using attenuated total reflection (ATR) sampling. The influence of anomalous dispersion on the IR-ATR spectra was evaluated by calculating the imaginary refractive index, k(ν), of each sample. Factor analysis (FA) was used to determine the number and abundance of species in the solutions. FA applied to both k(ν) spectra and IR-ATR spectra produced two principal spectra with a similar abundance of species. This result indicates that, even at high salt concentration, the optical effects do not influence the chemical analysis of IR-ATR spectra. The spectral modifications related to the salt concentrations are mainly first order. Second order effects were observed, but being weak, were not investigated. The two principal spectra are related to the two species present in the solution: pure water and CsCl-solvated water. From the latter, 2.8±0.4 water molecules were calculated to be associated with each close-bound Cs+/Cl- ion pair. In the case of KCl and NaCl aqueous solutions, both of which showed the same number of species, the number of water molecules associated to an ion pair was 5.0±0.4. That the latter number is different from that of CsCl indicates that the interaction between water molecules and ion pairs is different when cation Na or K in the chloride salt is replaced by Cs.

  17. Efficacy and Safety of Aluminum Chloride in Controlling External Hemorrhage: An Animal Model Study

    PubMed Central

    Nouri, Saeed; Sharif, Mohammad Reza; Panahi, Yunes; Ghanei, Mostafa; Jamali, Bardia

    2015-01-01

    Background: Despite all the progress in surgical science, bleeding caused by traffic accidents is still one of the challenges surgeons face in saving patients’ lives. Therefore, introducing an effective method to control external bleeding is an important research priority. Objectives: This study aimed to compare the hemostatic effect of aluminum chloride versus simple suturing in controlling external bleeding. Materials and Methods: This experimental study was conducted in Kashan, Iran. In this study, 60 male Wistar rats were randomly allocated into six groups. An incision, two centimeters (cm) long and half a cm deep, was made on each rat’s shaved back skin and the hemostatic time was measured once using aluminum chloride with different concentrations (5%, 10%, 15%, 25%, and 50%) and then using the control method (controlling hemorrhage by simple suturing). The skin tissue was assessed for pathological changes. Results: The hemostatic time of aluminum chloride 50%, 25%, 15%, 10% and 5% were 8.20 ± 0.919, 14.10 ± 1.37, 21.20 ± 1.31, 30.80 ± 1.68 and 42.00 ± 4.19 seconds, respectively. Also, the mean hemostasis time in the control group (suture) was 84.00 ± 4.05 seconds. The hemostatic times of different concentrations of aluminum chloride were significantly less than that of the control group. There was a statistically significant difference between every two hemostatic time. The pathologic examination showed the highest frequency of low-grade inflammation based on the defined pathological grading. Conclusions: The aluminum chloride method needs less time to control external hemorrhage compared to the control method (controlling external hemorrhage by simple suturing). Aluminum chloride is an effective agent in controlling external hemorrhage in an animal model. PMID:25964855

  18. Antimicrobial effects of an antiperspirant formulation containing aqueous aluminum chloride hexahydrate.

    PubMed

    Hölzle, E; Neubert, U

    1982-01-01

    To document deodorant efficacy the antimicrobial activity of a gelatinous antiperspirant formulation of aqueous aluminum chloride hexahydrate was investigated. In vitro assays demonstrated highly bactericidal activity on microorganisms comprising the resident axillary skin flora, including micrococcaceae and aerobic diphtheroid bacteria. Gram-negative bacteria and yeast were partially inhibited. In vivo experiments utilizing occlusive patches on forearm skin and bacterial sampling of the axilla showed pronounced bacteriostasis and persistence of aluminum chloride on the skin. Inhibition of microbial growth lasted more than 3 days after a single treatment of the axilla. Following repeated open applications to the volar aspect of the forearm, the skin remained virtually sterile for 3 days.

  19. Spectrofluorimetric determination of thallium in silicate rocks with rhodamine b in the presence of aluminum chloride

    USGS Publications Warehouse

    Shnepfe, M.M.

    1975-01-01

    A sensitive spectrofluorimetric procedure with rhodamine B in the presence of aluminum chloride is given for determining submicrogram and microgram quantities of thallium in silicate rocks. Samples are decomposed with a mixture of hydrofluoric and nitric acids and then treated with hydrochloric acid. Thallium is extracted as its dithizonate with chloroform from an alkaline medium containing ascorbate, citrate, and cyanide and then back-extracted with dilute nitric acid. After destruction of the organic matter and treatment with bromine, hydrochloric acid, aluminum chloride, and rhodamine B, the {A table is presented}. ?? 1975.

  20. Solution processed aluminum paper for flexible electronics.

    PubMed

    Lee, Hye Moon; Lee, Ha Beom; Jung, Dae Soo; Yun, Jung-Yeul; Ko, Seung Hwan; Park, Seung Bin

    2012-09-11

    As an alternative to vacuum deposition, preparation of highly conductive papers with aluminum (Al) features is successfully achieved by the solution process consisting of Al precursor ink (AlH(3){O(C(4)H(9))(2)}) and low temperature stamping process performed at 110 °C without any serious hydroxylation and oxidation problems. Al features formed on several kinds of paper substrates (calendar, magazine, and inkjet printing paper substrates) are less than ~60 nm thick, and their electrical conductivities were found to be as good as thermally evaporated Al film or even better (≤2 Ω/□). Strong adhesion of Al features to paper substrates and their excellent flexibility are also experimentally confirmed by TEM observation and mechanical tests, such as tape and bending tests. The solution processed Al features on paper substrates show different electrical and mechanical performance depending on the paper type, and inkjet printing paper is found to be the best substrate with high and stable electrical and mechanical properties. The Al conductive papers produced by the solution process may be applicable in disposal paper electronics.

  1. Microstructural Evolution of Chloride-Cleaned Silicon Carbide Aluminum Composites

    NASA Astrophysics Data System (ADS)

    Adeosun, S. O.; Akpan, E. I.; Gbenebor, O. P.; Balogun, S. A.

    2016-02-01

    This study examines the synergy between reinforcement surface modifications on the evolution of microstructures of AA6011-silicon carbide particle (SiCp) composites in multidirectional solidification. Silicon carbide particles (SiCp) were cleaned with ammonium chloride, tin(II) chloride, sodium chloride, and palladium(II) chloride and used as reinforcement to cast AA6011-SiCp composites by applying the stir casting method. A scanning electron microscope and x-ray diffractometer were used to investigate the morphology and phases present, respectively, in the composite material. Results show that wetting agents were effective as they inhibited the formation of Al4C3 in all modified composites. The modified SiCp was found to have varying effects on the morphology, dendrite arm size and direction, size and configuration of AlFeSi, and the amount of eutectic silicon depending on the concentration of the reagent and cleaning time. The highest effect was shown by the use of 40 g/L of tin(II) chloride. The composites had short dendritic arms, good interfacial interaction, and only a few crystals of AlFeSi.

  2. Reducing phosphorus in swine effluent with aluminum chloride treatment during lagoon cleanout

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Phosphorus (P) runoff from agricultural lands fertilized with swine manure can be a significant environmental issue. The objective of this study was to evaluate the effect of aluminum chloride (AlCl3) applications to a swine lagoon during total clean out on P concentrations in manure and runoff wat...

  3. Electrolysis of dilute sodium chloride solution in a diaphragm cell

    SciTech Connect

    Kubasov, V.L.; Ivanter, I.A.; Druzhinin, E.A.; Vorob'eva, V.B.

    1986-02-10

    In some cases, as in the production of iodine and bromine, dilute solutions of sodium chloride remain unutilized. In view of the existence of large amounts of unutilized spent sodium chloride solutions and their harmful effect when discharged into the environment, it is desirable to develop a process for production of chlorine and alkali with high current efficiencies, satisfying industrial requirements, from dilute sodium chloride solutions. The authors have therefore studied electrolysis of solutions containing 160 and 180 kg/m/sup 3/ of sodium chloride, having pH of 11.0-11.5, close in composition to solutions from the Cheleken chemical factory. The chlorine and alkali current efficiencies and the compositions of the anolyte, catholyte, and anode gas were determined.

  4. 46 CFR 151.50-75 - Ferric chloride solution.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Ferric chloride solution. 151.50-75 Section 151.50-75 Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY (CONTINUED) CERTAIN BULK DANGEROUS CARGOES BARGES CARRYING BULK LIQUID HAZARDOUS MATERIAL CARGOES Special Requirements § 151.50-75 Ferric chloride...

  5. 46 CFR 151.50-75 - Ferric chloride solution.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 46 Shipping 5 2014-10-01 2014-10-01 false Ferric chloride solution. 151.50-75 Section 151.50-75 Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY (CONTINUED) CERTAIN BULK DANGEROUS CARGOES BARGES CARRYING BULK LIQUID HAZARDOUS MATERIAL CARGOES Special Requirements § 151.50-75 Ferric chloride...

  6. 46 CFR 151.50-75 - Ferric chloride solution.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 46 Shipping 5 2012-10-01 2012-10-01 false Ferric chloride solution. 151.50-75 Section 151.50-75 Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY (CONTINUED) CERTAIN BULK DANGEROUS CARGOES BARGES CARRYING BULK LIQUID HAZARDOUS MATERIAL CARGOES Special Requirements § 151.50-75 Ferric chloride...

  7. 46 CFR 151.50-75 - Ferric chloride solution.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 46 Shipping 5 2011-10-01 2011-10-01 false Ferric chloride solution. 151.50-75 Section 151.50-75 Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY (CONTINUED) CERTAIN BULK DANGEROUS CARGOES BARGES CARRYING BULK LIQUID HAZARDOUS MATERIAL CARGOES Special Requirements § 151.50-75 Ferric chloride...

  8. 46 CFR 151.50-75 - Ferric chloride solution.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 46 Shipping 5 2013-10-01 2013-10-01 false Ferric chloride solution. 151.50-75 Section 151.50-75 Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY (CONTINUED) CERTAIN BULK DANGEROUS CARGOES BARGES CARRYING BULK LIQUID HAZARDOUS MATERIAL CARGOES Special Requirements § 151.50-75 Ferric chloride...

  9. Electrolytic conditioning of a magnesium aluminum chloride complex for reversible magnesium deposition

    SciTech Connect

    Barile, Christopher J.; Barile, Elizabeth C.; Zavadil, Kevin R.; Nuzzo, Ralph G.; Gewirth, Andrew A.

    2014-12-04

    We describe in this report the electrochemistry of Mg deposition and dissolution from the magnesium aluminum chloride complex (MACC). The results define the requirements for reversible Mg deposition and definitively establish that voltammetric cycling of the electrolyte significantly alters its composition and performance. Elemental analysis, scanning electron microscopy, and energy-dispersive X-ray spectroscopy (SEM-EDS) results demonstrate that irreversible Mg and Al deposits form during early cycles. Electrospray ionization-mass spectrometry (ESI-MS) data show that inhibitory oligomers develop in THF-based solutions. These oligomers form via the well-established mechanism of a cationic ring-opening polymerization of THF during the initial synthesis of the MACC and under resting conditions. In contrast, MACC solutions in 1,2-dimethoxyethane (DME), an acyclic solvent, do not evolve as dramatically at open circuit potential. Furthermore, we propose a mechanism describing how the conditioning process of the MACC in THF improves its performance by both tuning the Mg:Al stoichiometry and eliminating oligomers.

  10. Electrolytic conditioning of a magnesium aluminum chloride complex for reversible magnesium deposition

    DOE PAGES

    Barile, Christopher J.; Barile, Elizabeth C.; Zavadil, Kevin R.; ...

    2014-12-04

    We describe in this report the electrochemistry of Mg deposition and dissolution from the magnesium aluminum chloride complex (MACC). The results define the requirements for reversible Mg deposition and definitively establish that voltammetric cycling of the electrolyte significantly alters its composition and performance. Elemental analysis, scanning electron microscopy, and energy-dispersive X-ray spectroscopy (SEM-EDS) results demonstrate that irreversible Mg and Al deposits form during early cycles. Electrospray ionization-mass spectrometry (ESI-MS) data show that inhibitory oligomers develop in THF-based solutions. These oligomers form via the well-established mechanism of a cationic ring-opening polymerization of THF during the initial synthesis of the MACC andmore » under resting conditions. In contrast, MACC solutions in 1,2-dimethoxyethane (DME), an acyclic solvent, do not evolve as dramatically at open circuit potential. Furthermore, we propose a mechanism describing how the conditioning process of the MACC in THF improves its performance by both tuning the Mg:Al stoichiometry and eliminating oligomers.« less

  11. Stability of stored methacholine chloride solutions: clinically useful information.

    PubMed

    Pratter, M R; Woodman, T F; Irwin, R S; Johnson, B

    1982-10-01

    Methacholine inhalation challenge (MIC) has been shown to be an extremely useful diagnostic test. Because a decrease in the time and expense involved in the preparation of methacholine chloride solutions might encourage more laboratories to perform MIC, we assessed the stability of several different concentrations of methacholine chloride in solution over a period of 4 months. We used and compared 2 different assay techniques: a high pressure liquid chromatography assay and a colorimetric assay. Comparable results were obtained by both assays and demonstrated that methacholine solutions stored either at room temperature or at 4 degrees C showed no significant decomposition over a period of 4 months. From our results, we conclude that: (1) methacholine chloride solutions are much more stable than stated in the Merck Manual, (2) the original data of MacDonald and coworkers on the stability of methacholine chloride solution are accurate, (3) our high pressure liquid chromatography method is an accurate and highly specific technique for measuring methacholine chloride solutions. The major clinical implication of our results is that the time and cost necessary to prepare methacholine chloride solutions is much less than previously thought. This should encourage a more widespread use of this important diagnostic technique for the demonstration of bronchial hyperreactivity.

  12. Quantitative elemental analysis on aluminum accumulation by HVTEM-EDX in liver tissues of mice orally administered with aluminum chloride.

    PubMed

    Kametani, Kiyokazu; Nagata, Tetsuji

    2006-06-01

    Quantitative elemental analysis on Al was carried out by high-accelerating voltage transmission electron microscopy (HVTEM) equipped with energy-dispersive X-ray microanalysis (EDX) using an accelerating voltage at 300 kV with high permeability in 1-mum-thick samples obtained from mice administered with aluminum chloride solution for 3, 9, and 17 weeks. By light microscopic observation, no morphological changes were observed in the hepatocytes and macrophages in the liver tissues of mice that were administered with excess Al as compared with the normal control mice. In contrast, by electron microscopic observation, ultrastructural changes were observed in the lysosomes in the hepatocytes as well as the pinocytotic vesicles in the macrophages in the experimental animals. Therefore, the concentrations of Al detected in lysosomes in hepatocytes and pinocytotic vesicles in macrophages of livers of mice administered with Al were measured in relationship to those administration periods. Moreover, transitional changes of hepatocyte lysosome ratios by image analysis and the macrophage counts in the unit area increased in liver tissues of mice administered with Al as compared with normal control mice. From the results, it was demonstrated that hepatocyte lysosome ratio and macrophage count increased in liver tissues of treated mice during those short-term excessive Al administration periods. It was also clarified that the concentrations of Al in both hepatocytes and macrophages increased as observed by HVTEM-EDX. In conclusion, Al accumulated in hepatocytes and macrophages at 3 and 9 weeks administration, while the ultrastructural changes remained in the hepatocytes and macrophages. In contrast, Al concentration did not increase in the liver at 17 weeks administration.

  13. The evaporation of the water-sodium chlorides solution droplets on the heated substrate

    NASA Astrophysics Data System (ADS)

    Orlova, Evgenija; Kuznetsov, Geniy; Feoktistov, Dmitriy

    2014-08-01

    This work presents an experimental study of the evaporation of a sessile water- sodium chlorides solution drop to open atmosphere on the solid substrate (anodized aluminum) under the varying heat flux. The main parameters defining drop profile were obtained: contact diameter, contact angle, height of the drop. The specific evaporation rate was calculated. The influence of the initial concentration of the evaporated solution to a value of the specific evaporation rate has been found out. The specific evaporation rate decreases with increasing of the concentration.

  14. Stability of methacholine chloride in bronchial provocation test solutions.

    PubMed

    MacDonald, N C; Whitmore, C K; Makoid, M C; Cobby, J

    1981-06-01

    The stability of methacholine chloride (5 mg/ml) in 0.9% sodium chloride solution was measured. A reliable colorimetric assay (530 nm) based on the formation of a hydroxamic acid-iron complex was used. At appropriate time intervals, samples were removed from solutions stored at 4, 20, 37, 60, or 80 degrees C and assayed. The degradation of methacholine chloride followed apparent first-order kinetics of methacholine chloride followed apparent first-order kinetics at all temperatures, with observed half-lives ranging from 29.3 days at 80 degrees C to 693 days 4 degrees C. Methacholine chloride in 0.9% sodium chloride solution does not degrade as rapidly as previously suggested. According to an Arrhenius plot, storage of such solutions at 30 or 4 degrees C would result in not more than 10% degradation over a period of approximately two or five months, respectively. Thus, it should be possible to prepare stock solutions of this deliquescent drug.

  15. [Determination of Chloride Salt Solution by NIR Spectroscopy].

    PubMed

    Zhang, Bin; Chen, Jian-hong; Jiao, Ming-xing

    2015-07-01

    Determination of chloride salt solution by near infrared spectrum plays a very important role in Biomedicine. The near infrared spectrum analysis of Sodium chloride, potassium chloride, calcium chloride aqueous solution shows that the concentration change of chloride salt can affect hydrogen bond, resulting in the variation of near infrared spectrum of water. The temperature influence on NIR spectrum has been decreased by choosing reasonable wavelength range and the wavelength where the temperature effects are zero (isosbestic point). Chlorine salt prediction model was established based on partial least squares method and used for predicting the concentration of the chlorine ion. The impact on near infrared spectrum of the cation ionic radius, the number of ionic charge, the complex effect of ionic in water has also discussed in this article and the reason of every factor are analysed. Experimental results show that the temperature and concentration will affect the near-infrared spectrum of the solution, It is found that the effect of temperature plays the dominant role at low concentrations of chlorine salt; rather, the ionic dominates at high concentration. Chloride complexes are formed in aqueous solution, It has an effect on hydrogen bond of water combining with the cations in chlorine salt solution, Comparing different chloride solutions at the same concentration, the destruction effects of chloride complexes and catnions on the hydrogen bond of water increases in the sequences: CaCl2 >NaCl>KC. The modeling result shows that the determination coefficients (R2) = 99.97%, the root mean square error of cross validation (RM- SECV) = 4.51, and the residual prediction deviation (RPD) = 62.7, it meets the daily requirements of biochemical detection accuracy.

  16. Chemical milling solution produces smooth surface finish on aluminum

    NASA Technical Reports Server (NTRS)

    Lorenzen, H. C.

    1966-01-01

    Elementary sulfur mixed into a solution of caustic soda and salts produces an etchant which will chemically mill end-grain surfaces on aluminum plate. This composition results in the least amount of thickness variation and pitting.

  17. SOLVENT-FREE TETRAHYDROPYRANYLATION (THP) OF ALCOHOLS AND PHENOLS AND THEIR REGENERATION BY CATALYTIC ALUMINUM CHLORIDE HEXAHYDRATE

    EPA Science Inventory

    Catalytic amount of aluminum chloride hexahydrate enables solvent-free tetrahydropyranylation (THP) of alcohols and phenols at moderate temperatures. A simple addition of methanol helps to regenerate the corresponding alcohols and phenols thus rendering these protection and depro...

  18. Effect of chloride incorporation on the crystallization of zirconium-barium-lanthanum-aluminum fluoride glass

    NASA Technical Reports Server (NTRS)

    Neilson, G. F.; Smith, G. L.; Weinberg, M. C.

    1985-01-01

    One aspect of the influence of preparation procedure on the crystallization behavior of a zirconium-barium-lanthanum-aluminum fluoride glass was studied. The crystallization pattern of this glass may be affected by the chlorine concentration within it. In particular, when such glasses are heated at low temperatures, the alpha-Ba-Zr-F6 crystalline phase forms only in those glasses which contain chloride.

  19. The suppressive effects of aluminum chloride on the osteoblasts function.

    PubMed

    Zhu, Yanzhu; Xu, Feibo; Yan, Xijun; Miao, Liguang; Li, Haitao; Hu, Chongwei; Wang, Zhongying; Lian, Shizhen; Feng, Zhuo; Li, Yanfei

    2016-12-01

    Aluminum (Al) exposure impairs bone formation, and bone formation is mediated by the osteoblasts. But effects of Al on the osteoblasts function remain elusive. The osteoblasts were exposed to 0, 0.0252, 0.126, 0.252mg/mL AlCl3·6H2O for 24h. The osteoblasts viability, TGF-β1, BMP-2, IGF-I and Cbfα1 mRNA expressions, and GSH-Px and SOD activities, ROS concentration were determined. The osteoblasts ultrastructural features were also observed. The results showed that AlCl3 suppressed the osteoblasts viability, TGF-β1, BMP-2, IGF-I and Cbfα1 mRNA expressions, GSH-Px and SOD activities, and elevated ROS concentration compared with the CG. The ultrastructural features of osteoblasts in the HG showed mitochondrial swelling, foam-like structure, uneven distribution of chromatin, incomplete cell membrane and cytoplasm spillover compared with the CG. It indicates that AlCl3 inhibits osteoblasts viability, growth regulation factors mRNA expressions, anti-oxidative function, and damaged the osteoblasts histology structure, impairing the osteoblasts function.

  20. SOLVENT EXTRACTION PROCESS FOR URANIUM FROM CHLORIDE SOLUTIONS

    DOEpatents

    Blake, C.A. Jr.; Brown, K.B.; Horner, D.E.

    1960-05-24

    An improvement was made in a uranium extraction process wherein the organic extractant is a phosphine oxide. An aqueous solution containing phosphate ions or sulfate ions together with uranium is provided with a source of chloride ions during the extraction step. The presence of the chloride ions enables a phosphine oxide to extract uranium in the presence of strong uranium- complexing ions such as phosphate or sulfate ions.

  1. A Monte Carlo simulation of a supersaturated sodium chloride solution

    NASA Astrophysics Data System (ADS)

    Schwendinger, Michael G.; Rode, Bernd M.

    1989-03-01

    A simulation of a supersaturated sodium chloride solution with the Monte Carlo statistical thermodynamic method is reported. The water-water interactions are described by the Matsuoka-Clementi-Yoshimine (MCY) potential, while the ion-water potentials have been derived from ab initio calculations. Structural features of the solution have been evaluated, special interest being focused on possible precursors of nucleation.

  2. Electrical conductivity of acidic chloride solutions

    NASA Astrophysics Data System (ADS)

    Majima, Hiroshi; Peters, Ernest; Awakura, Yasuhiro; Park, Sung Kook; Aoki, Masami

    1988-02-01

    The electrical conductivities of aqueous solutions in the system HCl-MCln (where M = K, Na, Mg, Ni, or Cd) were measured at different temperatures. The equivalent electrical conductivity of H+ was calculated on the basis of simple assumptions for these solutions, and show an inverse relationship with water activity in these solutions. The results obtained by varying temperatures, solute ratios, and ionic strength on the electrical conductivity were found to be consistent with a proton jump mechanism for the H+ ion, where the activity of water is the most significant parameter affecting its equivalent conductance, and a viscous (Stokes’ law) drag mechanism (i.e., Walden’s rule is obeyed) for other ions found in acidic solutions.

  3. Aluminum compounds in calcium chloride extracts from podzolic soil and their possible sources

    NASA Astrophysics Data System (ADS)

    Tolpeshta, I. I.; Sokolova, T. A.

    2008-06-01

    Aluminum concentrations in organoaluminum complexes, mineral polymers, Al(H2O){6/3+}, Al(OH)(H2O){5/2+}, Al(OH)2(H2O){4/+}, AlH3SiO{4/2+}, and Al(OH)3(H2O){3/0} extracted with 0.001 M CaCl2 from the main genetic horizons of a podzolic soil on two-layered deposits were determined experimentally and calculated from thermodynamic equations. It was found that aluminum bound in organic complexes was predominant in extracts from the AE horizon, and mineral polymer aluminum compounds prevailed in extracts from the E and IIBD horizons. In the AE horizon, organoaluminum compounds were a major source of aluminum, which passed into solution predominantly by exchange reactions. In the E horizon, aluminum hydroxide interlayers in soil chlorites were the main source of aluminum, which passed into solution by dissolution reactions. In extracts from the IIBD horizon, aluminum was solubilized by the dissolution of aluminosilicates inherited from the parent rock.

  4. FIRE EXTINGUISHERS CONTAINING INHIBITED LITHIUM CHLORIDE SOLUTION FOR POLAR USE

    DTIC Science & Technology

    Previous experiments under this task using small metal test panels resulted in the selection of a sodium dichromate- oxalic acid inhibitor for use in...of drawn brass or silicon bronze and lined with a lead alloys, were tested with the lithium chloride solution using either sodium dichromate- oxalic ... acid or sodium dichromate alone as an inhibitor. It was determined that 0.5 percent sodium dichromate satisfactorily inhibits corrosion by the water solution of lithium chloride when contained in an extinguisher of drawn brass.

  5. Solution processed sodium chloride interlayers for efficient electron extraction from polymer solar cells

    NASA Astrophysics Data System (ADS)

    Nickel, Felix; Reinhard, Manuel; Zhang, Zhenhao; Pütz, Andreas; Kettlitz, Siegfried; Lemmer, Uli; Colsmann, Alexander

    2012-07-01

    We investigate a solution-processable, non-toxic sodium chloride (NaCl) interlayer for aluminum cathodes in organic solar cells. The electron extraction at the cathode interface is strongly improved upon the insertion of NaCl leading to power conversion efficiencies of up to 2.9% as compared to 1.8% efficient devices without interlayer. Scanning electron and kelvin probe force microscopy studies reveal that the formation of NaCl crystals causes a decrease of the aluminum work function by more than 300 mV. By impedance spectroscopy, we found evidence that the NaCl crystals improve the energetic alignment at the polymer/metal interface.

  6. Spectroscopic investigation of actinide speciation in concentrated chloride solution

    SciTech Connect

    Runde, W.; Neu, M.P.; Conradson, S.D.; Clark, D.L.; Palmer, P.D.; Reilly, S.D.; Scott, B.L.; Tait, C.D.

    1997-12-31

    The proposed disposal of nuclear waste in geological salt formations, e.g., the Waste Isolation Pilot Plant (USA) and the Gorleben site (Germany), raises a fundamental question: To what degree actinides will be solubilized and mobilized upon interaction with chloride ions? Actinide solubilities in highly concentrated chloride solutions are about one order of magnitude higher than in similar inert electrolyte (NaClO{sub 4}) solutions. This increased solubility is due to interactions between actinide and chloride ions. Contradictory results exist regarding the interaction mechanism between actinide and chloride ions. Specifically, both inner-sphere complex formation and ion pair association have been implicated in the interpretation of spectrophotometric and extraction data. To address this controversy, the authors investigated the interaction between actinide ions in the (III), (IV), (V) and (VI) oxidation states and chloride ions using a multi-method approach. Spectroscopic techniques (TRLFS, Raman, UV-Vis absorption, EXAFS) were used to distinguish between changes in the inner coordination sphere of the actinide ion and effects of ion pairing, X-ray absorption spectroscopy and single crystal X-ray diffraction were used to determine structural details of the actinide chloro complexes formed in solution and solid states.

  7. An equilibrium model for chloride removal from recycled cooling water using the ultra-high lime with aluminum process.

    PubMed

    Abdel-Wahab, Ahmed; Batchelor, Bill; Schwantes, Jon

    2005-01-01

    Removal of chloride from recycled cooling water is needed to reduce corrosion and prolong equipment life. Laboratory experiments have demonstrated that the ultra-high lime with aluminum (UHLA) process has the ability to achieve high chloride removal efficiency from recycled cooling water. In an effort to further understand the behavior of chloride in the UHLA process, a fundamental model of the chemical processes was developed. The purpose of this paper is to describe this equilibrium model and present values for solubility products of precipitated solids that have not been investigated previously. The model was based on PHREEQC and a new program called INVRS K was integrated with PHREEQC to calculate values of unknown or poorly defined equilibrium or kinetic constants using a Gauss-Newton nonlinear regression routine. Model predictions indicated that the results could be best described by assuming the formation of a solid solution of calcium chloroaluminate (Ca4Al2Cl2OH12), tricalcium hydroxyaluminate (Ca3Al2OH12), and tetracalcium hydroxyaluminate (Ca4Al2OH14).

  8. REMOVAL OF CHLORIDE FROM ACIDIC SOLUTIONS USING NO2

    SciTech Connect

    Visser, A; Robert Pierce, R; James Laurinat, J

    2006-08-22

    Chloride (Cl{sup -}) salt processing in strong acids is used to recycle plutonium (Pu) from pyrochemical residues. The Savannah River National Laboratory (SRNL) is studying the potential application of nitrogen dioxide (NO{sub 2}) gas to effectively convert dissolved pyrochemical salt solutions to chloride-free solutions and improve recovery operations. An NO{sub 2} sparge has been shown to effectively remove Cl{sup -} from solutions containing 6-8 M acid (H{sup +}) and up to 5 M Cl{sup -}. Chloride removal occurs as a result of the competition of at least two reactions, one which is acid-dependent. Below 4 M H+, NO2 reacts with Cl- to produce nitrosyl chloride (ClNO). Between 6 M and 8 M H{sup +}, the reaction of hydrochloric acid (HCl) with nitric acid (HNO{sub 3}), facilitated by the presence of NO{sub 2}, strongly affects the rate of Cl{sup -} removal. The effect of heating the acidic Cl{sup -} salt solution without pre-heating the NO{sub 2} gas has minimal effect on Cl{sup -} removal rates when the contact times between NO{sub 2} and the salt solution are on the order of seconds.

  9. Effects of organic solutes on chemical reactions of aluminum

    USGS Publications Warehouse

    Lind, Carol J.; Hem, John David

    1975-01-01

    Concentrations of organic matter in the general range of 1-10 milligrams per litre organic carbon are common in natural water, and many naturally occurrin7 organic compounds form aluminum complexes. The aluminum concentrations in near-neutral pH solutions may be 10-100 times higher than the values predicted from solubility data if formation of such organic complexes is ignored. The processes of polymerization of aluminum hydroxide and precipitation of gibbsite are inhibited by the presence of the organic flavone compound quercetin in concentrations as low as 10 x -5.3 mole per litre. Quercetin forms a complex, with a probable molar ratio of 1:2 aluminum to quercetin, that has a formation constant (f12) of about 10 12. A complex with a higher aluminum-quercetin ratio also was observed, but this material tends to evolve into a compound of low solubility that removes aluminum from solution. In the presence of both dissolved aluminum and aqueous silica, low concentrations of quercetin improved the yield of crystallized kaolinite and halloysite. Small amounts of well-shaped kaolinite and halloysite crystals were identified by electron microscopy in solutions with pH's in the range 6.5-8.5 after 155 days aging in one experimer t and 481 days aging in a repeated experiment. The bulk of the precipitated material was amorphous to X-rays, and crystalline material was too small a proportion of the total to give identifiable X-ray diffraction peaks. The precipitates had aluminum-silicon ratios near 1, and their solubility corresponded to that found by Hem, Roberson, Lind, and Polzer (1973) for similar aluminosilicate precipitated in the absence of organic solutes. The improved yield of crystalline material obtained in the presence of quercetin probably is the result of the influence of the organic compound on the aluminum hydroxide polymerization process. Natural water containing color imparted by organic material tends to be higher in aluminum than would be predicted by p

  10. Polarization of the lithium electrode in sulfuryl chloride solutions

    NASA Astrophysics Data System (ADS)

    Alessandrini, F.; Scrosati, B.; Croce, F.; Lazzari, M.; Bonino, F.

    1983-05-01

    The growth of the passivating film on a lithium electrode in contact with sulfuryl chloride solutions has been examined by micropolarization and complex impedance measurements. The results tend to confirm the hypothesis of a two-layer film, where probably the first layer is thin and compact and the second layer is porous and defective.

  11. Tetragonal Chicken Egg White Lysozyme Solubility in Sodium Chloride Solutions

    NASA Technical Reports Server (NTRS)

    Forsythe, Elizabeth L.; Judge, Russell A.; Pusey, Marc L.

    1998-01-01

    The solubility of chicken egg white lysozyme, crystallized in the tetragonal form was measured in sodium chloride solutions from 1.6 to 30.7 C, using a miniature column solubility apparatus. Sodium chloride solution concentrations ranged from 1 to 7% (w/v). The solutions were buffered with 0.1 M sodium acetate buffer with the solubility being measured at pH values in 0.2 pH unit increments in the range pH 4.0 to 5.4, with data also included at pH 4.5. Lysozyme solubility was found to increase with increases in temperature and decreasing salt concentration. Solution pH has a varied and unpredictable effect on solubility.

  12. Acid hydrolysis of cellulose in zinc chloride solution

    SciTech Connect

    Cao, N.J.; Xu, Q.; Chen, L.F.

    1995-12-31

    The efficient conversion of cellulosic materials to ethanol has been hindered by the low yield of sugars, the high energy consumption in pretreatment processes, and the difficulty of recycling the pre-treatment agents. Zinc chloride may provide an alternative for pre-treating biomass prior to the hydrolysis of cellulose. The formation of a zinc-cellulose complex during the pretreatment of cellulose improves the yield of glucose in both the enzymatic and acid hydrolysis of cellulose. Low-temperature acid hydrolysis of cellulose in zinc chloride solution is carried out in two stages, a liquefaction stage and a saccharification stage. Because of the formation of zinc-cellulose complex in the first stage, the required amount of acid in the second stage has been decreased significantly. In 67% zinc chloride solution, a 99.5% yield of soluble sugars has been obtained at 70{degrees}C and 0.5M acid concentration. The ratio of zinc chloride to cellulose has been reduced from 4.5 to 1.5, and the yield of soluble sugars is kept above 80%. The rate of hydrolysis is affected by the ratio of zinc chloride to cellulose, acid concentration, and temperature.

  13. Contribution of interstitial solute strengthening in aluminum

    NASA Astrophysics Data System (ADS)

    Matsui, Isao; Ono, Satoshi; Hanaoka, Yudai; Uesugi, Tokuteru; Takigawa, Yorinobu; Higashi, Kenji

    2014-02-01

    Enthalpies of solutions and misfit strains for the Al-X (X = H, B, C, N, and O) binary alloys were determined by first-principles calculations to estimate the strengthening of solid solutions caused by interstitial atoms. The results indicate that interstitial solute atoms produced large misfit strains. Electrodeposited Al containing 0.12-1.32 at.% C was used to assess the validity of solid-solution strengthening by interstitial solute atoms. The role that interstitial carbon plays in strengthening electrodeposited Al is discussed.

  14. Ginkgo biloba extract alleviates oxidative stress and some neurotransmitters changes induced by aluminum chloride in rats.

    PubMed

    Mohamed, Naglaa El-Shahat; Abd El-Moneim, Ahmed E

    2017-03-01

    In the present study, twenty four adult male albino rats were classified into four groups. The control group received normal diet and water; the second group was treated daily with oral dose of Ginkgo biloba (200 mg/kg body weight [b.wt]) for 3 mo; the third group was treated daily with oral dose of aluminum chloride (10 mg/kg b.wt) for 3 mo; and the fourth group was treated with both Ginkgo biloba and aluminum chloride (200 and 10 mg/kg b.wt, respectively) using a stomach tube for 3 mo. The results showed that administration of AlCl3 to rats induced significant increase (P < 0.05) in thiobarbituric acid reactive substance and decrease (P < 0.05) in glutathione, catalase, and superoxide dismutase in brain and testis homogenates. The data also showed significant decrease (P < 0.05) in noradrenaline, dopamine, and serotonin (5-HT) levels in brain tissue. The rats administered AlCl3 showed significant decrease (P < 0.05) in serum zinc (Zn) and copper (Cu), significant increase (P < 0.05) in serum iron (Fe), and non-significant decrease in magnesium (Mg). Furthermore, significant increase (P < 0.05) in serum alkaline phosphatase and acid phosphatase and significant decrease (P < 0.05) in testosterone were recorded. The histologic examination showed some degenerative changes in both brain and testis tissues while significant improvement in biochemical and histologic changes were observed in the aluminum chloride plus Ginkgo biloba group. It could be concluded that the protective effect of Ginkgo biloba may be attributed to its antioxidant properties.

  15. Hydration patterns and salting effects in sodium chloride solution

    NASA Astrophysics Data System (ADS)

    Li, Weifeng; Mu, Yuguang

    2011-10-01

    The salting effects of 2M sodium chloride electrolyte are studied based on a series of model solutes with properties ranging from hydrophobic to hydrophilic. Generally, hydrophobic solutes will be salted out and hydrophilic solutes will be salted in by NaCl solution. The solvation free energy changes are highly correlated with Kirkwood-Buff integrals. The underlying mechanism resorts to the preferential binding of ions and water to solutes. Our results demonstrate that the salting effect not only depends on the salt's position in Hofmeister series, but also on the solutes' specifics. Taking the hydration free energies of solutes and ions as independent variables, a schematic diagram of salting effects is suggested. The resolved multifaceted salting effects rely on the sensitive balance of the tripartite interaction among solutes, ions, and water.

  16. Hydration patterns and salting effects in sodium chloride solution.

    PubMed

    Li, Weifeng; Mu, Yuguang

    2011-10-07

    The salting effects of 2M sodium chloride electrolyte are studied based on a series of model solutes with properties ranging from hydrophobic to hydrophilic. Generally, hydrophobic solutes will be salted out and hydrophilic solutes will be salted in by NaCl solution. The solvation free energy changes are highly correlated with Kirkwood-Buff integrals. The underlying mechanism resorts to the preferential binding of ions and water to solutes. Our results demonstrate that the salting effect not only depends on the salt's position in Hofmeister series, but also on the solutes' specifics. Taking the hydration free energies of solutes and ions as independent variables, a schematic diagram of salting effects is suggested. The resolved multifaceted salting effects rely on the sensitive balance of the tripartite interaction among solutes, ions, and water.

  17. Absorption characteristics of elemental mercury in mercury chloride solutions.

    PubMed

    Ma, Yongpeng; Xu, Haomiao; Qu, Zan; Yan, Naiqiang; Wang, Wenhua

    2014-11-01

    Elemental mercury (Hg(0)) in flue gases can be efficiently captured by mercury chloride (HgCl2) solution. However, the absorption behaviors and the influencing effects are still poorly understood. The mechanism of Hg(0) absorption by HgCl2 and the factors that control the removal were studied in this paper. It was found that when the mole ratio of Cl(-) to HgCl2 is 10:1, the Hg(0) removal efficiency is the highest. Among the main mercury chloride species, HgCl3(-) is the most efficient ion for Hg(0) removal in the HgCl2 absorption system when moderate concentrations of chloride ions exist. The Hg(0) absorption reactions in the aqueous phase were investigated computationally using Moller-Plesset perturbation theory. The calculated Gibbs free energies and energy barriers are in excellent agreement with the results obtained from experiments. In the presence of SO3(2-) and SO2, Hg(2+) reduction occurred and Hg(0) removal efficiency decreased. The reduced Hg(0) removal can be controlled through increased chloride concentration to some degree. Low pH value in HgCl2 solution enhanced the Hg(0) removal efficiency, and the effect was more significant in dilute HgCl2 solutions. The presence of SO4(2-) and NO3(-) did not affect Hg(0) removal by HgCl2.

  18. Inactivation of biological agents using neutral oxone-chloride solutions.

    PubMed

    Delcomyn, Carrie A; Bushway, Karen E; Henley, Michael V

    2006-04-15

    Bleach solutions containing the active ingredient hypochlorite (OCl-) serve as powerful biological disinfectants but are highly caustic and present a significant compatibility issue when applied to contaminated equipment or terrain. A neutral, bicarbonate-buffered aqueous solution of Oxone (2K2HSO5.KHSO4.K2SO4) and sodium chloride that rapidly generates hypochlorite and hypochlorous acid (HOCl) in situ was evaluated as a new alternative to bleach for the inactivation of biological agents. The solution produced a free chlorine (HOCl + OCl-) concentration of 3.3 g/L and achieved > or =5.8-log inactivation of spores of Bacillus atrophaeus, Bacillus thuringiensis, Aspergillus niger, and Escherichia coli vegetative cells in 1 min at 22 degrees C. Seawaterwas an effective substitute for solid sodium chloride and inactivated 5 to 8 logs of each organism in 10 min over temperatures ranging from -5 degrees C to 55 degrees C. Sporicidal effectiveness increased as free chlorine concentrations shifted from OCl- to HOCl. Neutrally buffered Oxone-chloride and Oxone-seawater solutions are mitigation alternatives for biologically contaminated equipment and environments that would otherwise be decontaminated using caustic bleach solutions.

  19. An XAFS Study of Nickel Chloride in the Ionic Liquid 1-ethyl-3-methyl Imidazolium Chloride/ Aluminum Chloride

    SciTech Connect

    Roeper, D.; Cheek, G; Pandya, K; O'Gragy, W

    2008-01-01

    The electrodeposition of metals from aqueous solutions has a successful history for many metals. However, some metals cannot be deposited from aqueous solutions because their potentials fall outside of the window of stability for water. Using ionic liquids for the electrodeposition of metals can avoid some of these difficulties because they have a larger region of stability than water. The electrochemical window can be tailored to fit a particular application by choosing appropriate anions and cations to form the melt. There is also the possibility to deposit pure metals without the oxides and hydrides that can form in aqueous solutions. The study of the structure of metal salts in ionic liquids is an important step towards achieving these goals.

  20. Low coverage spontaneous etching and hyperthermal desorption of aluminum chlorides from Cl2/Al(111).

    PubMed

    Grassman, Tyler J; Poon, Gary C; Kummel, Andrew C

    2004-11-08

    Nonresonant multiphoton ionization with time-of-flight mass spectrometry has been used to monitor the desorption of aluminum chloride (Al(x)Cl(y)) etch products from the Al(111) surface at 100 and 500 K during low-coverage (<5% monolayer) monoenergetic Cl(2) (0.11-0.65 eV) dosing. The desorption products in this low-coverage range show predominantly hyperthermal exit velocities under all dosing conditions. For example, with 0.27 eV incident Cl(2), the etch product was found to have a most-probable velocity of 517+/-22 m/s at an Al(111) surface temperature of 100 K. This corresponds to 22 times the expected thermal desorption translational energy for AlCl(3). Cl(2) sticking probability measurements and Al(x)Cl(y) etch rate measurements show etching even at Cl(2) coverages of less than 5% monolayer at surface temperatures between 100 and 500 K. These experimental results are consistent with a combination of fast-time-scale surface diffusion and agglomeration of the adsorbed chlorine to form aluminum chlorides and the presence of activated AlCl(3) chemisorption states having potential energies above the vacuum level. Density functional theory calculations yield results that are consistent with both our experimental findings and mechanistic descriptions.

  1. Protective effect of a calcium channel blocker "diltiazem" on aluminum chloride-induced dementia in mice.

    PubMed

    Rani, Anu; Neha; Sodhi, Rupinder K; Kaur, Amanpreet

    2015-11-01

    Many studies report that heavy metals such as aluminum are involved in amyloid beta aggregation and neurotoxicity. Further, high concentration of aluminum in the brain deregulates calcium signaling which contributes to synaptic dysfunction and halts neuronal communication which ultimately leads to the development of Alzheimer's disease. Recently, diltiazem, a calcium channel blocker clinically used in angina, is reported to decrease amyloid beta production by inhibiting calcium influx, decreasing inflammation and oxidative stress. However, the probable role of this drug in aluminum chloride (AlCl3)-induced experimental dementia is yet to be explored. Therefore, the present study is designed to investigate the effect of AlCl3-induced dementia in mice. Morris water maze test and elevated plus maze were utilized to evaluate learning and memory. Various biochemical estimations including brain acetylcholinesterase activity (AChE), brain total protein, thiobarbituric acid-reactive species (TBARS) level, reduced glutathione (GSH) level, nitrate/nitrite, and superoxide dismutase (SOD) were measured. AlCl3 significantly impaired learning and memory and increased brain AChE, brain total protein, TBARS, and nitrate/nitrite and decreased brain GSH or SOD. On the other hand, treatment with diltiazem significantly reversed AlCl3-induced behavioral and biochemical deficits. The present study indicates the beneficial role of diltiazem in AlCl3-induced dementia.

  2. Multi-scale modelling of uranyl chloride solutions

    SciTech Connect

    Nguyen, Thanh-Nghi; Duvail, Magali Villard, Arnaud; Dufrêche, Jean-François; Molina, John Jairo; Guilbaud, Philippe

    2015-01-14

    Classical molecular dynamics simulations with explicit polarization have been successfully used to determine the structural and thermodynamic properties of binary aqueous solutions of uranyl chloride (UO{sub 2}Cl{sub 2}). Concentrated aqueous solutions of uranyl chloride have been studied to determine the hydration properties and the ion-ion interactions. The bond distances and the coordination number of the hydrated uranyl are in good agreement with available experimental data. Two stable positions of chloride in the second hydration shell of uranyl have been identified. The UO{sub 2}{sup 2+}-Cl{sup −} association constants have also been calculated using a multi-scale approach. First, the ion-ion potential averaged over the solvent configurations at infinite dilution (McMillan-Mayer potential) was calculated to establish the dissociation/association processes of UO{sub 2}{sup 2+}-Cl{sup −} ion pairs in aqueous solution. Then, the association constant was calculated from this potential. The value we obtained for the association constant is in good agreement with the experimental result (K{sub UO{sub 2Cl{sup +}}} = 1.48 l mol{sup −1}), but the resulting activity coefficient appears to be too low at molar concentration.

  3. Spectroscopy of UO2Cl42- in basic aluminum chloride: 1-ethyl-3-methylimidazolium chloride

    NASA Astrophysics Data System (ADS)

    Hopkins, Todd A.; Berg, John M.; Costa, David A.; Smith, Wayne H.; Dewey, Harry J.

    2000-07-01

    In this study we focus on the spectroscopic characterization of UO2Cl42- in 40:60 AlCl3:EMIC using multiple techniques. A combination of absorption, emission, excitation, two-photon excitation, Fourier transform Raman, and time-resolved emission spectra for solution (298 K) and frozen glass (75 K) samples have been measured and analyzed in terms of the electronic and vibrational structures of the UO2Cl42- ion. The spectroscopic properties of UO2Cl42- in single crystals are well known, and the analyses of the spectra of UO2Cl42- in 40:60 AlCl3:EMIC rely heavily on single crystal studies. Results are also compared with absorption spectra from a previous study of UO2Cl42- in 48:52 AlCl3:EMIC (a basic ionic liquid). The results from multiple spectroscopic measurements and their comparison with previous results help provide a picture of the structure and environment of UO2Cl42- in 40:60 AlCl3:EMIC.

  4. Raman Study of Aluminum Chloride-Dimethylsulfone Solutions.

    PubMed

    Legrand, L.; Tranchant, A.; Messina, R.; Romain, F.; Lautie, A.

    1996-02-28

    The Raman spectra of AlCl(3)-LiCl-dimethylsulfone mixtures with different molar compositions have been recorded as a solid (300 K) and as a melt (400 K). In any case, only AlCl(4)(-) ion lines at 120, 179, and 347 cm(-)(1) were observed; we were unable to detect any other chloroaluminate species. Furthermore, some bands assigned to the Al[(CH(3))(2)SO(2)](3)(3+) octahedral coordination compound are evidence for a high AlCl(3) content.

  5. Spectrofluorimetric determination of trace aluminum in diluted hemodialysis solutions

    NASA Astrophysics Data System (ADS)

    Gündüz, S. Beniz; Küçükkolbaşý, Semahat; Atakol, Orhan; Kýlýç, Esma

    2005-03-01

    In this study, a spectrofluorimetric method has been developed for the determination of aluminum based on the formation of an aluminum complex with N, N'-disalicylidene-1,3-diamino-2-hydroxypropane (DSAHP). The most suitable pH, solvent medium, complex formation time, Schiff base concentration and temperature were determined. The excitation and emission wavelengths were 270 and 437 nm, respectively, in which the DSAHP-Al complex gave the maximum flurescence intensity at pH 3.0 and 6.0 in 50% dioxan-50% water medium. Under these conditions, calibration curves were obtained in three different linear limits, and was found that aluminum could be detected within the concentration limit of 0-10.0 μM and the lowest detection limit being 0.27 ng ml -1. The stochiometry of the DSAHP-Al complex was also determined spectrofluorimetrically under optimal conditions and the molar ratio of DSAHP-Al was calculated as 2:1. Using the developed method, aluminum was detected in hemodialysis solutions, and the results obtained were similar and comparable with those obtained using the method described in the British Pharmacopoeia within 95% confidence limits. This method can be used successfully for the routine determination of aluminum because it is quick, requires less amount of reactives, is sensitive, reliable and reproducible.

  6. Use of modified hydroxy-aluminum bentonites for chromium(III) removal from solutions.

    PubMed

    Volzone, Cristina; Beatriz Garrido, Liliana

    2008-09-01

    The retention of chromium(III) from a 2,000 ppm chromium basic sulfate and tannery waste solution at pH 4.5 using modified hydroxy-aluminum bentonites (OH-Al bentonites) as adsorbents was studied. OH-Al bentonite was prepared by mixing clay with a hydrolyzed commercial chlorohydroxy Al solution. The modified Al bentonites were obtained by (a) a treatment with 0.5M sodium chloride and (b) a treatment with a Na-hexametaphosphate solution (HMP) after adding sodium chloride. The effect of heating the adsorbents at 100, 500, 700 and 800 degrees C on Cr retention as a function of time was also analyzed. Cr retention by modified OH-Al bentonite with HMP increased with time (up to 100 mg Cr/g) where modified OH-Al bentonite was twice that of untreated bentonite. The relatively high uptake of metal from the salt solution by modified OH-Al bentonite treated at 800 degrees C, in which a complete interlayer collapse occurred, indicated the importance of the contribution of external surface sites to the retention capacity. The maximum Cr uptake from a water waste was 24 mg/g, due to interferences and different chromium species in the industrial solution.

  7. Structure of concentrated aqueous solutions of scandium chloride

    NASA Astrophysics Data System (ADS)

    Smirnov, P. R.; Grechin, O. V.

    2017-03-01

    It is shown via X-ray diffraction that aqueous solutions of scandium chloride form ionic associates in a wide range of concentrations. It is established that the Sc3+ ion coordination number increases upon dilution to 8.2 at an unchanged Sc3+-OH2 distance of 0.215 nm. The second coordination sphere of the cation forms at an average distance of 0.420 nm. The number of solvent molecules in the sphere logically increases during dilution. It is concluded that the anion does not form its own sphere in highly concentrated solutions. This coordination sphere begins to form only in solutions with moderate concentrations at a distance of 0.315 nm, and it contains six water molecules in diluted solutions.

  8. Regulation of aerobic granular sludge reformulation after granular sludge broken: effect of poly aluminum chloride (PAC).

    PubMed

    Liu, Yongjun; Liu, Zhe; Wang, Fukun; Chen, Yiping; Kuschk, Peter; Wang, Xiaochang

    2014-04-01

    The present study focuses on the effect of poly aluminum chloride (PAC) on the re-formation of aerobic granular sludge after its rupture. The morphological changes, physical characteristics such as SVI, mechanical strength and surface properties of aerobic granular sludge during the re-formation process of broken granules were investigated. Moreover, components (protein (PN), polysaccharides (PS)) and distributions (soluble, loosely-bound (LB), tightly-bound (TB)) of extracellular polymeric substances (EPS) in sludge flocs were taken into consideration. It was found that the effect of charge neutralization and bridging induced by PAC treatment improved the surface properties of sludge, the re-formed granules had a larger size, more compact structure and that the removal performance of pollutants after chemical coagulation had improved. The results of correlation analysis demonstrated that PN in EPS correlated well with the surface characteristics and settling ability of sludge flocs, and PAC treatment strengthened the influence, further accelerated the reformation of granular sludge.

  9. Electrochemical Behavior of Copper in Thionyl Chloride Solutions.

    DTIC Science & Technology

    1980-12-01

    lithium - thionyl chloride batteries . Thionyl chloride is known *3 to react...electrolyte for lithium - thionyl chloride batteries . 8R. K. McAlpine and B. A. Soule, Prescott and Johnson’s Qualitative Chemical Analysis, D. Van...black carbon electrodes, cupric chloride appears to be a useful cathode additive for lithium - thionyl chloride batteries . Preliminary results2l

  10. Form and stability of aluminum hydroxide complexes in dilute solution

    USGS Publications Warehouse

    Hem, John David; Roberson, Charles Elmer

    1967-01-01

    Laboratory studies of solutions 4.53 x 10 -4 to 4.5 x 10 -5 molal (12.2-1.2 ppm) in aluminum, in 0.01 molal sodium perchlorate, were conducted to obtain information as to the probable behavior of aluminum in natural water. When the solutions were brought to pH 7.5-9.5 and allowed to stand for 24 hours, a precipitate was obtained which was virtually amorphous as shown by X-rays, and which had a solubility equivalent to that of boehmite. This precipitate had a hydrolysis constant (*Ks4) of 1.93 x 10 -13a. When solutions were allowed to stead at this pH range for 10 days, their precipitates gave the X-ray pattern of bayerite (*Ks4 = 1.11 > (10- 4). These hydrolysis constants were obtained at 25?C. and corrected to zero ionic strength and are in close agreement with other published values. The predominant dissolved form in this pH range is Al(OH) -4. Below neutral pH (7.0) the dissolved aluminum species consist of octahedral units in which each aluminum ion is surrounded by six water molecules or hydroxide ions. Single units such as Al(OH2)6 + 3 and AlOH(OH2)5+2 are most abundant below pH 5.0, and where the molar ratio (r) of combined hydroxide to total dissolved aluminum is low. When r is greater than 1.0, polymerization of the octahedral units occurs. When r is between 2.0 and 3.0, solutions aged for 10 days or more contained colloidal particles between 0.10 and 0.45 ? in diameter. Particles whose diameters were greater than 0.10 ? were identified by X-ray diffraction as gibbsite. Particles smaller than 0.10 ? were also present and were shown by means of the electron microscope to have a hexagonal crystal pattern. Structured material consisting of sheets of coalesced six-membered rings of aluminum ions held together by double OH bridges has a distinctive kinetic behavior. This property was used to determine amounts of polymerized material in solutions having r between 1.0 and 3.0 after aging times ranging from a few hours to more than 4 months. Aging increased the

  11. The use of synthetic hydrocalcite as a chloride-ion getter for a barrier aluminum anodization process

    SciTech Connect

    Panitz, J.K.G.; Sharp, D.J.

    1995-11-01

    Chloride ion contamination at parts per billion concentrations plaques electrochemists studying barrier anodic aluminum oxide film growth and anodic aluminum oxide capacitor manufacturers. Chloride ion contamination slows film growth and reduces film quality. We have demonstrated that synthetic hydrocalcite substantially reduces the detrimental effects of chloride ion contamination in an aqueous electrolyte commonly used to grow barrier anodic aluminum oxide. We have determined that problems arise if precautions are not taken when using synthetic hydrocalcite as a chloride-ion getter in an aqueous electrolyte. Synthetic hydrocalcite is somewhat hydrophobic. If this powder is added directly to an aqueous electrolyte, some powder disperses; some floats to the top of the bath and forms scum that locally impedes anodic film formation. Commercially available powder contains a wide range of particle sizes including submicrometer-sized particles that can escape through filters into the electrolyte and cause processing problems. These problems can be over come if (1) the getter is placed in filter bags, (2) a piece of filter paper is used to skim trace amounts of getter floating on the top of the bath, (3) dummy runs are performed to scavenge chloride-ion loaded getter micelles dispersed in the bath, and (4) substrates are rinsed with a strong stream of deionized water to remove trace amounts of powder after anodization.

  12. The Use of Sodium Chloride & Aluminum as Phase Change Materials for High Temperature Thermal Energy Storage Characterized by Calorimetry

    NASA Astrophysics Data System (ADS)

    Solomon, Laura

    2013-01-01

    Encapsulated phase change materials (EPCM) have a great deal of potential for the storage of thermal energy in a wide range of applications. The present work is aimed at developing encapsulated phase change materials capable of storing thermal energy at temperatures above 700°C for use in concentrated solar power (CSP) systems. EPCM with a phase change material (PCM) with both a salt (sodium chloride) and a metal (aluminum) are considered here. Sodium chloride and aluminum are effective storage mediums because of their high melting points and large latent heats of fusion, 800°C and 660°C and 430kJ/kg and 397kJ/kg, respectively. Based on the heat capacities and the latent heat of fusion, for a 100 degree temperature range centered on the melting point of the PCM, 80% of the energy stored by the sodium chloride PCM can be attributed to the latent heat and 79% for the aluminum PCM. These large fractions attributed to latent heat have the potential for making EPCM based thermal energy storage devices smaller and less expensive. To study the performance of the candidate PCMs considered here, a specialized immersion calorimeter was designed, calibrated, and used to evaluate the storage capabilities of sodium chloride and aluminum based EPCMs. Additionally, the EPCMs were studied to ensure no loss of capacity would occur over the lifetime of the EPCM. While no reduction in the storage capacity of the sodium chloride EPCMs was found after repeated thermal cycles, there was a decrease in the storage capacity of the aluminum EPCMs after prolonged exposure to high temperatures.

  13. Evaluation of cetylpyridinium chloride for infection control in storage solution.

    PubMed

    Ziskind, D; Gleitman, J; Rotstein, I; Friedman, M

    2003-05-01

    Storage solution is used in in vitro experimental studies to prevent dehydration of teeth collected immediately after extraction and to prevent bacterial and fungal growth in the storage media. The chemical nature of the storing agent may affect the tooth structure and material properties at the tested interface. The aim of this study was to evaluate the use of 0.1% cetylpyridinium chloride (CPC) as a new storage solution and to assess the possible effect of 0.1% thymol on microleakage and bond strength. Forty extracted human teeth were collected from 10 different dental clinics. Immediately after extraction, the teeth were randomly divided and immersed in four different storage solutions. Two test solutions of 0.1% CPC (group C) and 0.1% thymol (group T) were compared with phosphate-buffered saline (Group S - positive control) and to 3% H2O2 (group H - negative control). Bond strength test and dye penetration evaluation were then carried out. The findings suggest that the use of 0.1% CPC as storage solution does not affect bond strength to enamel. However, it may increase dye penetration at the cervical margin. The effect of 0.1% thymol on shear bond strength and dye penetration is similar to the effect of phosphate-buffered saline.

  14. Effect of aluminum chloride and dietary phytase on relative ammonia losses from swine manure.

    PubMed

    Smith, D R; Moore, P A; Haggard, B E; Maxwells, C V; Daniel, T C; VanDevander, K; Davis, M E

    2004-02-01

    Ammonia (NH3) losses from swine manure contribute to odor problems, decrease animal productivity, and increase the risk of acid rain deposition. This study was conducted to determine whether aluminum chloride (AlCl3) or dietary manipulation with phytase could decrease relative NH3 losses from swine manure. Twenty-four pens of nursery pigs were used in two trials, and the pigs were fed normal or phytase-supplemented (500 IU/kg) diets. Aluminum chloride was added to manure pits (1.9 x 1.2 x 0.5 m) under each pen at 0, 0.25, 0.50, or 0.75% (vol:vol) of final manure volume. Manure pH and NH3 losses (measured by relative NH3 flux) were determined twice weekly. The addition of AlCl3 at 0.75% decreased (P < 0.05) manure pH from 7.48 to 6.69. Phytase decreased (P < 0.05) manure pH to 7.07 compared with 7.12 in the normal diet manure. Aluminum chloride administered at 0.75% without phytase reduced (P < 0.05) relative NH3 losses 52% for the entire 6-wk period. Relative NH3 losses were decreased (P < 0.05) from 109 mg of NH3/(m2 x h) in pens containing pigs fed the normal diet without AlCl3 to 81 mg of NH3/(m2 x h) in pens housing pigs administered the phytase diet, a 26% reduction. When the phytase diet and 0.75% AlCl3 additions were used in combination, relative NH3 losses were reduced (P < 0.05) by 60% compared with pens of pigs fed the control diet without AlCl3. Decreases in manure pH were likely responsible for the observed reduction in NH3 losses. Multiple regression was performed with relative rates of NH3 losses as the dependent variable and rate of AlCl3 addition, diet, and manure pH as independent variables. The model was tested using a stepwise regression (P < 0.001), and results indicated that the most important factors determining NH3 losses were manure pH and diet. However, the contribution of AlCl3 cannot be discounted. When manure pH was regressed against AlCl3 and dietary phytase, AlCl3 levels accounted for 64% of the variation in manure pH (P < 0

  15. Comparison of repassivation kinetics of stainless steels in chloride solution

    NASA Astrophysics Data System (ADS)

    Park, Chan-Jin; Kwon, Hyuk-Sang

    2005-08-01

    Using a rapid scratching electrode technique, the repassivation kinetics of type 304, 316, 444, and 2205 stainless steels (SS) were investigated in a chloride solution. The value of cBV in a log i(t) versus 1/q(t) plot as an effective measure of the repassivation rate was used to compare the reapssivation behaviors among the alloys. During repassivation, lower values of cBV for SS corresponded with faster repassivation rates with the formation of a more protective passive film. In a comparison of repassivation rates based on the alloy's cBV values, the best repassivation behavior was shown by 2205 SS, followed by 444 SS and 316 SS. However, 304 SS exhibited an inflection point in the log i(t) versus 1/q(t) curve, suggesting that dissolution by localized corrosion rather than SCC may occur in the alloy under given conditions.

  16. Polyene Formation Catalyzed by Phosphotungstic Acid and Aluminum Chloride in Thin Films of Poly(Vinyl Alcohol)

    NASA Astrophysics Data System (ADS)

    Tretinnikov, O. N.; Sushko, N. I.; Maly, A. B.

    2016-01-01

    Formation of linear polyenes -(CH=CH) n - during thermal dehydration of thin layers (9-20 μm) of poly(vinyl alcohol) containing phosphotungstic-acid and aluminum-chloride catalysts was investigated. It was found that the concentration of long-chain ( n ≥ 8) polyenes in films containing phosphotungstic acid increased smoothly with increasing annealing time although the kinetics of the dehydration were independent of the film thickness. The polyene ( n ≥ 8) formation rate in films containing aluminum chloride dropped quickly with decreasing film thickness and increasing annealing time. As a result, long-chain polyenes practically did not form regardless of the annealing time for a film thickness of 11 μm.

  17. Reaction of 1-chloro-1-methylcyclohexane with phenyl- and benzyl-trimethylsilanes in the presence of aluminum chloride

    SciTech Connect

    Bolestova, G.I.; Parnes, Z.N.; Vol'pin, M.E.

    1988-10-20

    In the reaction of 1-chloro-1-methylcyclohexane with phenyltrimethylsilane and benzyltrimethylsilane in the presence of aluminum chloride the chlorine atom is substituted by a phenyl or benzyl group with the formation of 1-methyl-1-phenyl- and 1-methyl-1-benzylcyclohexane, respectively. In the case of benzyltrimethylsilane the products from alkylation of the benzene ring of the benzyltrimethylsilane by the 1-methylcyclohexyl carbocation in the Friedel-Crafts reaction are formed in addition to 1-methyl-1-benzylcyclohexane.

  18. Flocculation of low algae concentration water using polydiallyldimethylammonium chloride coupled with polysilicate aluminum ferrite.

    PubMed

    Lv, Liping; Zhang, Xiaodong; Qiao, Junlian

    2017-03-08

    The combined application of polydiallyldimethylammonium chloride (PDADMAC) and polysilicate aluminum ferrite (PSFA) was investigated to treat low algae density water samples, in which Microcystis aeruginosa is one of the dominant species. coagulation performance of M. aeruginosa was studied with regard to algal removal, Algal density was evaluated by determining the change in the optical density of the algal culture suspension at 680 nm and chlorophyll a. The dissolved organic matter, cellular morphology, viability, and recovery of M. aeruginosa cells after flocculation and sedimentation were also included. In addition, the effects of pH and addition order of PSFA and PDADMAC on algal removal were investigated. The removal efficiency of algae coagulated using combined PDADMAC and PSFA was improved by 34.5% and 19.3%, respectively. The organic matter removal was also enhanced. The optimum pH range for algal removal is 7.0-10.0, and the preferable addition sequence is the simultaneous addition of PDADMAC and PSFA. Scanning electron microscopy observation indicated that the combined usage of PDADMAC and PSFA caused no damage to the algal cell. Moreover, the experiment on algal recovery demonstrated that PDADMAC has bacteriostatic ability.

  19. Electrical, dielectric and electrochemical measurements of bulk aluminum phthalocyanine chloride (AlPcCl)

    NASA Astrophysics Data System (ADS)

    Soliman, I. M.; El-Nahass, M. M.; Mansour, Y.

    2016-01-01

    AC conductivity and the related dielectric properties of bulk aluminum phthalocyanine chloride (AlPcCl) have been studied over a temperature range (303-403 K) and frequency range (42-106 Hz). The universal power law σac (ω)=Aωs has been used to investigate dependence of AC conductivity on frequency. The variation of the frequency exponent (s) with temperature was analyzed in terms of different conduction mechanisms; the predominant conduction mechanism was found to be the correlated barrier hopping (CBH) model. The barrier height was calculated by using (CBH) model, it was found to be 1.41 eV. Dependence of σac (ω) on temperature refers to a linear increase with increasing temperature at different frequencies. The density of states N (EF) was calculated to be equal 4.11×1019 cm-3 using Elliott model. It has been found that AC activation energy decreases with increasing frequency. Dielectric values were analyzed using complex permittivity and complex electric modulus for bulk AlPcCl at different temperatures. The obtained value of HOMO-LUMO energy gap was found to be 1.48 eV.

  20. Enhanced coagulation for improving coagulation performance and reducing residual aluminum combining polyaluminum chloride with diatomite.

    PubMed

    Hu, Wenchao; Wu, Chunde

    2016-01-01

    The feasibility of using enhanced coagulation, which combined polyaluminum chloride (PAC) with diatomite for improving coagulation performance and reducing the residual aluminum (Al), was discussed. The effects of PAC and diatomite dosage on the coagulation performance and residual Al were mainly investigated. Results demonstrated that the removal efficiencies of turbidity, dissolved organic carbon (DOC), and UV254 were significantly improved by the enhanced coagulation, compared with PAC coagulation alone. Meaningfully, the five forms of residual Al (total Al (TAl), total dissolved Al (TDAl), dissolved organic Al (DOAl), dissolved monomeric Al (DMAl), and dissolved organic monomeric Al (DOMAl)) all had different degrees of reduction in the presence of diatomite and achieved the lowest concentrations (0.185, 0.06, 0.053, 0.014, and 0 mg L(-1), respectively) at a PAC dose of 15 mg L(-1) and diatomite dose of 40 mg L(-1). In addition, when PAC was used as coagulant, the majority of residual Al existed in dissolved form (about 31.14-70.16%), and the content of DOMAl was small in the DMAl.

  1. Protective effect of resveratrol against aluminum chloride induced nephrotoxicity in rats

    PubMed Central

    Dera, Hussain S. Al

    2016-01-01

    Objectives: To investigate the potential protective effect of resveratrol (RES) on aluminum chloride (AlCl3)-induced nephrotoxicity in rats. Methods: This experimental study was conducted from April to June 2015 at the Medical College of King Khalid University, Abha, Kingdom of Saudi Arabia. The experiments were performed on 24 male Wistar rats. The rats were randomly allocated into 4 groups; 1) group A: control rats received only normal saline, 2) group B: received RES dissolved in normal saline, 3) group C: model group and received AlCl3 dissolved in normal saline and 4) group D: RES treated group and received concomitant doses of RES+AlCl3. All treatments were administered for consecutive 40 days. After 40 days of treatments, kidney function tests, oxidative stress parameters and histopathological assay were evaluated. Results: all findings clearly showed significant deteriorations in kidney function and architectures after AlCl3 exposure. This was accompanied by increased renal oxidative stress and inflammation suggesting strong pro-oxidant activity of AlCl3 in spite of its non-redox status. Resveratrol co-treatment with AlCl3 to the rats showed significant improvement in all biochemical and histological parameters related to kidney function and structure. Conclusion: The findings of the current study showed that RES pre-administration to rats ameliorates renal damage and improves renal function in AlCl3 intoxicated rats in a mechanism related to its antioxidant potential. PMID:27052279

  2. Aluminum chloride as a solid is not a strong Lewis acid.

    PubMed

    Murthy, J Krishna; Gross, Udo; Rüdiger, Stephan; Rao, V Venkat; Kumar, V Vijaya; Wander, A; Bailey, C L; Harrison, N M; Kemnitz, Erhard

    2006-04-27

    Aluminum chloride is used extensively as Lewis acid catalyst in a variety of industrial processes, including Friedel-Crafts and Cl/F exchange reactions. There is a common misconception that pure AlCl3 is itself a Lewis acid. In the current study, we use experimental and computational methods to investigate the surface structure and catalytic properties of solid AlCl3. The catalytic activity of AlCl3 for two halide isomerization reactions is studied and compared with different AlF3 phases. It is shown that pure solid AlCl3 does not catalyze these reactions. The (001) surface of crystalline AlCl(3) is the natural cleavage plane and its structure is predicted via first principles calculations. The chlorine ions in the outermost layer of the material mask the Al3+ ions from the external gas phase. Hence, the experimentally found catalytic properties of pure solid AlCl3 are supported by the predicted surface structure of AlCl3.

  3. Solution phase synthesis of aluminum-doped silicon nanoparticles via room-temperature, solvent based chemical reduction of silicon tetrachloride

    NASA Astrophysics Data System (ADS)

    Mowbray, Andrew James

    We present a method of wet chemical synthesis of aluminum-doped silicon nanoparticles (Al-doped Si NPs), encompassing the solution-phase co-reduction of silicon tetrachloride (SiCl4) and aluminum chloride (AlCl 3) by sodium naphthalide (Na[NAP]) in 1,2-dimethoxyethane (DME). The development of this method was inspired by the work of Baldwin et al. at the University of California, Davis, and was adapted for our research through some noteworthy procedural modifications. Centrifugation and solvent-based extraction techniques were used throughout various stages of the synthesis procedure to achieve efficient and well-controlled separation of the Si NP product from the reaction media. In addition, the development of a non-aqueous, formamide-based wash solution facilitated simultaneous removal of the NaCl byproduct and Si NP surface passivation via attachment of 1-octanol to the particle surface. As synthesized, the Si NPs were typically 3-15 nm in diameter, and were mainly amorphous, as opposed to crystalline, as concluded from SAED and XRD diffraction pattern analysis. Aluminum doping at various concentrations was accomplished via the inclusion of aluminum chloride (AlCl3); which was in small quantities dissolved into the synthesis solution to be reduced alongside the SiCl4 precursor. The introduction of Al into the chemically-reduced Si NP precipitate was not found to adversely affect the formation of the Si NPs, but was found to influence aspects such as particle stability and dispersibility throughout various stages of the procedure. Analytical techniques including transmission electron microscopy (TEM), FTIR spectroscopy, and ICP-optical emission spectroscopy were used to comprehensively characterize the product NPs. These methods confirm both the presence of Al and surface-bound 1-octanol in the newly formed Si NPs.

  4. Evaluation of aluminum indices to predict aluminum toxicity to plants grown in nutrient solutions

    SciTech Connect

    Alva, A.K.; Blamey, F.P.C.; Edwards, D.G.; Asher, C.J.

    1986-01-01

    Difficulty has been experienced in establishing a suitable aluminum (Al) index to predict Al toxicity to plants grown in nutrient solutions with a wide range of properties. In the present study, relationships were evaluated between root length and (i) concentration of total Al, (ii) concentration of monomeric Al, and (iii) the sum of the activities of monomeric Al species (..sigma..a/sub Al mono/) in solution. Results are reported for soybean (Glycine max (L.) Merr.), subterranean clover (Trifolium subterraneum L.), alfalfa (Medicago sativa L.), and sunflower (Helianthus annuus L.). Total Al concentration in solution, comprising polymeric and monomeric Al species, was a poor index of Al toxicity, confirming the hypothesis that only monomeric Al is toxic to root growth. In solutions with widely differing composition, the concentration of monomeric Al also proved unsatisfactory due to ionic strength effects on the activities of monomeric Al species. ..sigma..a/sub Al mono/ was the best index of Al toxicity, accounting for 72 to 92% of the variation in root length depending on the plant species. Root length was reduced by 50% at ..sigma..a/sub Al mono/ of 7-16 ..mu..M in soybean, 13 ..mu..M in subterranean clover and alfalfa, and 11 ..mu..M in sunflower.

  5. Localized corrosion of stainless steels in ammonium chloride solutions

    SciTech Connect

    Forsen, O.; Aromaa, J.; Tavi, M.; Virtanen, J.

    1997-05-01

    Ammonium chloride deposition is a well-known problem in oil refining. When these deposits form in a moist environment, they are corrosive to carbon steel. When unexpected corrosion problems are faced, the material is often changed to alloys like stainless steels (SS). Electrochemical measurements were used to study the corrosion resistance of SS in ammonium chloride environments with different chloride contents and at different temperatures.

  6. Purification of aqueous plutonium chloride solutions via precipitation and washing.

    SciTech Connect

    Stroud, M. A.; Salazar, R. R.; Abney, Kent David; Bluhm, E. A.; Danis, J. A.

    2003-01-01

    Pyrochemical operations at Los Alamos Plutonium Facility (TA-55) use high temperature melt s of calcium chloride for the reduction of plutonium oxide to plutonium metal and hi gh temperature combined melts of sodium chloride and potassium chloride mixtures for the electrorefining purification of plutonium metal . The remaining plutonium and americium are recovered from thes e salts by dissolution in concentrated hydrochloric acid followed by either solvent extraction or io n exchange for isolation and ultimately converted to oxide after precipitation with oxalic acid . Figur e 1 illustrates the current aqueous chloride flow sheet used for plutonium processing at TA-55 .

  7. Process for producing gallium-containing solution from the aluminum smelting dust

    SciTech Connect

    Era, A.; Matsui, S.; Ikeda, H.

    1988-03-01

    A process is described for producing a gallium-containing solution from aluminum smelting dust comprising leaching aluminum smelting dust with a mineral acid selected from the group consisting of sulfuric acid, hydrochloric acid and nitric acid, and adding an oxidizing agent to the aluminum smelting dust at the time of leaching to preferentially leach and extract gallium from the aluminum smelting dust without extracting aluminum from the aluminum smelting dust. The oxidizing agent is selected from the group consisting of potassium permanganate, manganese dioxide, hydrogen peroxide, ozone, potassium chromate, potassium dichromate, ammonium persulfate, sodium hydrochlorite, sodium chlorite and sodium chlorate. The leached aluminum smelting dust is filtered to obtain a gallium-containing solution of dissolved gallium.

  8. Application of aluminum chloride phthalocyanine-loaded solid lipid nanoparticles for photodynamic inactivation of melanoma cells.

    PubMed

    Goto, Patrícia L; Siqueira-Moura, Marigilson P; Tedesco, Antonio C

    2017-02-25

    Cutaneous melanoma is the most aggressive skin cancer and is particularly resistant to current therapeutic approaches. Photodynamic therapy (PDT) is a well-established photoprocess that is employed to treat some cancers, including non-melanoma skin cancer. Aluminum chloride phthalocyanine (ClAlPc) is used as a photosensitizer in PDT; however, its high hydrophobicity hampers its photodynamic activity under physiological conditions. The aim of this study was to produce solid lipid nanoparticles (SLN) containing ClAlPc using the direct emulsification method. ClAlPc-loaded SLNs (ClAlPc/SLNs) were characterized according to their particle size and distribution, zeta potential, morphology, encapsulation efficiency, stability, and phototoxic action in vitro in B16-F10 melanoma cells. ClAlPc/SLN had a mean diameter between 100 and 200nm, homogeneous size distribution (polydispersity index <0.3), negative zeta potential, and spherical morphology. The encapsulation efficiency was approximately 100%. The lipid crystallinity was investigated using X-ray diffraction and differential scanning calorimetry and indicated that ClAlPc was integrated into the SLN matrix. The ClAlPc/SLN formulations maintained their physicochemical stability without expelling the drug over a 24-month period. Compared to free ClAlPc, ClAlPc/SLN exerted outstanding phototoxicity effects in vitro against melanoma cells. Therefore, our results demonstrated that the ClAlPc/SLN described in the current study has the potential for use in further preclinical and clinical trials in PDT for melanoma treatment.

  9. A potentiodynamic study of aluminum-lithium alloys in an aqueous sodium chloride environment

    NASA Technical Reports Server (NTRS)

    Tsao, C.-H. T.; Pizzo, P. P.

    1985-01-01

    The characteristics of the potentiodynamic curves for Al-Li alloys in 3.5 percent NaCl aqueous solution are explained and the electrochemical parameters of the potentiodynamic technique are correlated to observed pitting and intergranular cracking behavior. It is shown that the oxygen content of the sodium chloride electrolyte plays an important role in the electrochemical behavior of Al-Li alloys. The potentiodynamic behavior of the alloys is found to be insensitive to variation in compositional content and heat treatment, both of which affect the stress-corrosion behavior. Stringer oxide particle attack and random pitting are observed. It is shown that alternate-immersion exposure prior to potentiodynamic polarization may offer a means of assessing susceptibility to stress-corrosion cracking.

  10. Sonolytic desorption of mercury from aluminum oxide: effects of pH, chloride, and organic matter.

    PubMed

    He, Ziqi; Traina, Samuel J; Weavers, Linda K

    2007-02-01

    The effects of pH, Cl-, and humic acid (HA) on sonolytic desorption of Hg(II) from aluminum oxide were examined. Results showed that Hg(II) desorption was achieved by lowering the pH from 7.0 to 4.0. Ultrasound enhanced Hg(II) release at short times compared to both hydrodynamic mixing and that expected on the basis of the pH-dependent Hg(II) adsorption curve. However, prolonged sonication led to decreases in Hg(II) desorption due to occlusion by aluminum hydroxide precipitation induced by ultrasound. The presence of Cl- greatly improved Hg(II) desorption at pH 4.0 due to the formation of stable nonadsorbing HgCl2(0) complexes at low pH, reducing free Hg(II) ion in solution. However, Cl- did not affect Hg(ll) desorption at pH 8.0, where Hg(OH)2(0) is the dominant Hg species rather than HgCl2(0). Hg(ll) desorption from HA-laden Al2O3 was dominated by HA. The greater the desorption of HA, the greater the desorption of Hg(II). Ultrasound enhanced the initial Hg(II) release by facilitating HA desorption. However, decreases in Hg(II) desorption were observed over longer sonication times due to the sonochemically induced reassociation of desorbed HA back onto Al2O3. Information obtained in this study provides insight into understanding sonolytic release of Hg from Hg-contaminated particles and sediments.

  11. Memory recuperative potential of rifampicin in aluminum chloride-induced dementia: role of pregnane X receptors.

    PubMed

    Kaur, P; Sodhi, R K

    2015-03-12

    The present study has been designed to investigate the potential of rifampicin [Pregnane X receptors (PXR) agonist] in experimental dementia. Aluminum chloride (AlCl3) [100mg/kg, p.o. for 42days] was administered to Wistar rats (n=6) to induce dementia. Morris water maze (MWM) test was used to assess learning and memory and rota rod test was used to assess locomotor activity of the animals. A battery of biochemical tests and histopathological evaluation using hematoxylin and eosin (H&E) and Congo Red stains were performed at the end of the study. AlCl3-treated rats demonstrated impaired cognition and locomotor activity on MWM apparatus and rota rod test, respectively. These animals exhibited a significant rise in acetylcholinesterase (AChE) activity (138±3.6), thiobarbituric acid reactive species (TBARS) level (15±1.6), nitrite (56±2.4) level and myeloperoxidase (MPO) activity (4.1±0.9) along with decline in reduced glutathione (GSH) level (22±1.3) in comparison to the control group (p<0.05). Further the H&E and Congo Red-stained cerebral cortex sections of AlCl3-treated rats indicated severe neutrophilic infiltration and amyloid deposition. Rifampicin-treated AlCl3-rats exhibited significant attenuation in memory deficits, biochemical parameters like AChE activity (33±1.4), TBARS level (4.1±1.0), nitrite level (64±2.6), MPO activity (3.6±1.0) and GSH level (53±2.4) along with improved histopathological alterations and locomotor activity when compared with AlCl3-treated rats (p<0.05). Combined administration of ketoconazole (a PXR antagonist) and rifampicin to AlCl3-treated animals reversed the rifampicin-induced protective effects. Therefore the results obtained from the study indicate a defensive role of rifampicin in memory dysfunction which may probably be due to its anti-cholinesterase, anti-oxidative, anti-inflammatory and amyloid lowering effects. Moreover the study speculates the potential of PXR in the pathophysiology of dementia which is subject

  12. Solution-Derived, Chloride-Containing Minerals as a Waste Form for Alkali Chlorides

    SciTech Connect

    Riley, Brian J.; Crum, Jarrod V.; Matyas, Josef; McCloy, John S.; Lepry, William C.

    2012-10-01

    Sodalite [Na8(AlSiO4)6Cl2] and cancrinite [(Na,K)6Ca2Al6Si6O24Cl4] are environmentally stable, chloride-containing minerals and are a logical waste form option for the mixed alkali chloride salt waste stream that is generated from a proposed electrochemical separations process during nuclear fuel reprocessing. Due to the volatility of chloride salts at moderate temperatures, the ideal processing route for these salts is a low-temperature approach such as the sol-gel process. The sodalite structure can be easily synthesized by the sol-gel process; however, it is produced in the form of a fine powder with particle sizes on the order of 1–10 µm. Due to the small particle size, these powders require additional treatment to form a monolith. In this study, the sol-gel powders were pressed into pellets and fired to achieve > 90% of theoretical density. The cancrinite structure, identified as the best candidate mineral form in terms of waste loading capacity, was only produced on a limited basis following the sol-gel process and converted to sodalite upon firing. Here we discuss the sol-gel process specifics, chemical durability of select waste forms, and the steps taken to maximize chloride-containing phases, decrease chloride loss during pellet firing, and increase pellet densities.

  13. Theoretical calculation of positron affinities of solute clusters in aluminum alloys

    NASA Astrophysics Data System (ADS)

    Mizuno, Masataka; Araki, Hideki; Shirai, Yasuharu

    2016-01-01

    We have performed theoretical calculations of positron states for solute clusters in aluminum alloys to estimate the positron affinity of solute clusters. Positron states of solute clusters in aluminum alloys were calculated under the electronic structures obtained by first- principles molecular orbital calculations using Al158-X13 clusters. We defined the positron affinity of the solute clusters by the difference in the lowest potential sensed by positrons between the solute clusters and Al bulk. With increasing atomic number of 3d metals, the annihilation fraction of the solute clusters rapidly increases at Mn and shows a maximum at Ni. A similar trend is observed for 4d metals. The localization of positron at the solute clusters mainly arises from charge transfer from Al matrix to solute clusters. The positron affinity defined in this work well represents the localization of positron at the solute clusters in aluminum alloys.

  14. Doping effect of human blood on surface microstructure of cupric chloride dendrites grown from aqueous solutions

    NASA Astrophysics Data System (ADS)

    Shibata, Takashi; Takakuwa, Yuichi; Tanaka, Akemi; Iguchi, Tomiko; Kogure, Mitsuko; Ogawa, Tomoya

    1996-10-01

    Surface microstructures of cupric chloride dendrites grown in aqueous solutions without and with doping of blood obtained from healthy individuals showed remarkable differences when studied by atomic force microscopy.

  15. Kinetics of photobleaching of aqueous solutions of ricin agglutinin in the presence of guanidine chloride

    NASA Astrophysics Data System (ADS)

    Brandt, Nikolai N.; Chikishev, Andrey Y.

    2002-05-01

    Kinetics of background decay in Raman spectra of aqueous solutions of ricin agglutinin in the presence of guanidine chloride were measured. The differences in the kinetics of photobleaching are discussed.

  16. Formation of linear polyenes in poly(vinyl alcohol) films catalyzed by phosphotungstic acid, aluminum chloride, and hydrochloric acid

    NASA Astrophysics Data System (ADS)

    Tretinnikov, O. N.; Sushko, N. I.; Malyi, A. B.

    2016-07-01

    Formation of linear polyenes-(CH=CH)n-via acid-catalyzed thermal dehydration of polyvinyl alcohol in 9- to 40-µm-thick films of this polymer containing hydrochloric acid, aluminum chloride, and phosphotungstic acid as dehydration catalysts was studied by electronic absorption spectroscopy. The concentration of long-chain ( n ≥ 8) polyenes in films containing phosphotungstic acid is found to monotonically increase with the duration of thermal treatment of films, although the kinetics of this process is independent of film thickness. In films containing hydrochloric acid and aluminum chloride, the formation rate of polyenes with n ≥ 8 rapidly drops as film thickness decreases and the annealing time increases. As a result, at a film thickness of less than 10-12 µm, long-chain polyenes are not formed at all in these films no matter how long thermal duration is. The reason for this behavior is that hydrochloric acid catalyzing polymer dehydration in these films evaporates from the films during thermal treatment, the evaporation rate inversely depending on film thickness.

  17. Selenium Alleviates Oxidative Stress and Lung Damage Induced by Aluminum Chloride in Adult Rats: Biochemical and Histological Approach.

    PubMed

    Ghorbel, Imen; Elwej, Awatef; Chaabane, Mariem; Jamoussi, Kamel; Mnif, Hela; Boudawara, Tahia; Zeghal, Najiba

    2017-03-01

    Our study pertains to the potential ability of selenium, used as a nutritional supplement, to alleviate oxidative stress induced by aluminum chloride in the lung tissue. Rats have received during 21 days either aluminum chloride (AlCl3) (400 ppm) via drinking water, AlCl3 associated with Na2SeO3 (0.5 mg/kg of diet), or only Na2SeO3. Exposure of rats to AlCl3 induced lung oxidative stress with an increase of malondialdehyde, hydrogen peroxide, and protein carbonyls levels. An alteration of lactate dehydrogenase activities and antioxidant redox status, enzymatic (catalase, superoxide dismutase, and glutathione peroxidase), and non-enzymatic (non-protein thiols, glutathione, metallothionein, and vitamin C) was also observed. These biochemical modifications were substantiated by histopathological data showing alveolar edema, a large number of hemosiderin-laden macrophages, and emphysema. Se supplementation attenuated the levels of oxidative stress by restoring antioxidant state and improved lung histological damage. Our results revealed that Se, a trace element with antioxidant properties, was effective in preventing lung damage.

  18. Application of phosphorus-31 and aluminum-27 NMR spectroscopic techniques to study aqueous and methanolic solutions of tetraphenylammonium aluminophosphate

    NASA Astrophysics Data System (ADS)

    Goudarzi, Nasser; Amin, Amir H.

    2017-01-01

    In this work, aluminum-27 and phosphorus-31 NMR spectroscopic techniques were used to investigate and characterize the distribution of aluminophosphate (AlPO) species soluble in the aqueous and methanolic solutions of tetraphenylammonium (TPhA) chloride. The reaction between hexaaquaaluminum cations, [A1(H2O)6]3+, and different phosphate ligands such as H3PO4, H2PO4-, and the acidic dimers H6P2O8 and H5P2O8- resulted in the formation of the soluble AlPO cations. The effective aluminum-27 and phosphorous-31 NMR spectroscopies can be employed to characterize the species present in a solution. Assignment of the peaks present in the aluminum-27 NMR spectra to the aluminate species or aluminate connectivities was done to acquire information about different AlPO complexes. Some resonance lines were observed in the phosphorus-31 {1H} NMR spectra, indicating the existence of different complexes in the AlPO solutions. Some peaks were observed in the methanolic solutions of AlPO at the chemical shifts of -0.41, -6.4, -7.5, -7.9, -13.1, -13.9, -16.6, -18.1, and -20.6 ppm. Four additional peaks were also observed in the phosphorus-31 {1H} NMR spectra of the methanolic solutions of AlPO, whose intensities changed with changes in the methanol:water volume ratio; they were observed in methanol but not in aqueous AlPO.

  19. A diffusive anomaly of water in aqueous sodium chloride solutions at low temperatures.

    PubMed

    Kim, Jun Soo; Yethiraj, Arun

    2008-02-14

    Molecular dynamics simulations are presented for the self-diffusion coefficient of water in aqueous sodium chloride solutions. At temperatures above the freezing point of pure water, the self-diffusion coefficient is a monotonically decreasing function of salt concentration. Below the freezing point of pure water, however, the self-diffusion coefficient is a non-monotonic function of salt concentration, showing a maximum at approximately one molal salt. This suggests that sodium chloride, which is considered a structure-making salt at room temperature, becomes a structure-breaking salt at low temperatures. A qualitative understanding of this effect can be obtained by considering the effect of ions on the residence time of water molecules near other water molecules. A consideration of the freezing point depression of aqueous sodium chloride solutions suggests that the self-diffusion coefficient of water in supercooled sodium chloride solutions is always higher than that in pure (supercooled) water at the same temperature.

  20. Aluminum modifies the viscosity of filamentous actin solutions as measured by optical displacement microviscometry.

    PubMed

    Arnoys, E J; Schindler, M

    2000-01-01

    A microtechnique has been developed that is capable of measuring the viscosity of filamentous actin (F-actin) solutions. This method, called optical displacement microviscometry (ODM), was utilized to determine the changes in viscosity of solutions of rabbit muscle, human platelet, and maize pollen actin when measured in the absence and presence of aluminum. Measurements demonstrated that the viscosity of the different actin solutions decreased with aluminum concentration. In contrast, increases in viscosity were observed when aluminum was added to F-actin solutions containing filamin (chicken gizzard), a protein that bundles actin filaments. Confocal fluorescence imaging of pure actin solutions in the presence of aluminum showed a disrupted actin network composed of fragmented actin filaments in the form of small aggregates. In contrast, in the presence of filamin, aluminum promoted the formation of thicker actin filaments. These measurements demonstrate that aluminum can affect actin filaments differentially depending on the presence of an actin-binding protein. In addition, a strong correlation is observed between the changes in viscosity as measured by ODM and the thickness and assembled state of bundles of actin filaments.

  1. Aluminum-induced changes in properties and fouling propensity of DOM solutions revealed by UV-vis absorbance spectral parameters.

    PubMed

    Zhou, Minghao; Meng, Fangang

    2016-04-15

    The integration of pre-coagulation with ultrafiltration (UF) is expected to not only reduce membrane fouling but also improve natural organic matter (NOM) removal. However, it is difficult to determine the proper coagulant dosage for different water qualities. The objective of this study was to probe the potential of UV-vis spectroscopic analysis to reveal the coagulant-induced changes in the fouling potentials of dissolved organic matter (DOM) and to determine the optimal coagulant dosage. The Zeta potentials (ZPs) and average particle size of the four DOM solutions (Aldrich humic acid (AHA), AHA-sodium alginate (SA), AHA-bovine serum albumin (BSA) and AHA-dextran (DEX)) coagulated with aluminum chloride (AlCl3) were measured. Results showed that increasing the aluminum coagulant dosage induced the aggregation of DOM. Meanwhile, the addition of aluminum coagulant resulted in an increase in DSlope(325-375) (the slope of the log-transformed absorbance spectra from 325 to 375 nm) and a decrease in S(275-295) (the slope of the log-transformed absorption coefficient from 275 to 295 nm) and SR (the ratio of Slope(275-295) and Slope(350-400)). The variations of these spectral parameters (i.e., DSlope(325-375), S(275-295) and SR) correlated well with the aluminum-caused changes in ZPs and average particle size. This implies that spectral parameters have the potential to indicate DOM aggregation. In addition, good correlations of spectral parameters and membrane fouling behaviors (i.e., unified membrane fouling index (UMFI)) suggest that the changes in DSlope(325-375), S(275-295) and SR were indicative of the aluminum-caused alterations of fouling potentials of all DOM solutions. Interestingly, the optimal dosage of aluminum (40 μM for AHA, AHA-BSA, and AHA-DEX) was obtained based on the relation between spectral parameters and fouling behaviors. Overall, the spectroscopic analysis, particularly for the utilization of spectral parameters, provided a convenient approach

  2. Flocculation kinetics mechanism and floc formation prepared by poly aluminum chloride coupled with polyacrylamide for ship ballast water.

    PubMed

    Zhou, Zhimin; Liu, Sha; Jia, Linan

    2016-01-01

    The performance of flocculants prepared by poly aluminum chloride (PAC) and polyacrylamide (PAM) on treating ballast water collected at the Dalian new port area, the evaluation depending on the values of reaction parameters, and kinetics mechanism of flocculation were investigated in this study. Accordingly, the flocculants of 0.1 g·L(-1), prepared by mixing PAC of 10% with PAM of 2.0‰, enabled the removal rate of zooplankton and phytoplankton to reach 91% in ballast water at 20 °C. Based on flocculation kinetics mechanism analysis, the efficient vortex size during stirring should be larger than the floc particles, and gradient of fluctuating velocity provide the impetus for turbulence flocculation. The results of this study could be relevant to understanding particle-floc interactions during developmental flocculation, and during application of ballast water treatment.

  3. Effect of natural dissolved organic carbon on phosphate removal by ferric chloride and aluminum sulfate treatment of wetland waters

    NASA Astrophysics Data System (ADS)

    Qualls, Robert G.; Sherwood, Lindsay J.; Richardson, Curtis J.

    2009-09-01

    The use of wetlands for the removal of excess N and P has become widespread. Some sensitive P-limited ecosystems, however, may require additional reductions in the concentration of P entering the system. It has been proposed that the treatment of wetlands through addition of ferric chloride or aluminum sulfate can augment the natural P removal mechanisms. However, high concentrations of natural dissolved organic matter may interfere with the removal of P by metal addition. We evaluated the doses of ferric chloride and aluminum sulfate necessary to reduce total P concentrations below 0.32 μM (10 μg/L) in water from the Northern Everglades, and we determined the effect of various concentrations (21, 38, and 60 mg/L) of natural dissolved organic carbon (DOC) on the removal of PO4 and total P. High concentrations of natural DOC inhibited both the short-term removal of PO4 and the longer-term removal of total P from the water column. Similar results were observed using 15 μM citric acid in an experiment to determine whether citric acid could effectively mimic the inhibition of phosphorus removal associated with natural DOC. Stoichiometry of these experiments indicates that the mechanism of natural DOC interference was not complexation of the metal ions by the DOC; we hypothesize that it could be adsorption to the terminal hydroxyl groups on a polynuclear Fe or Al colloid, effectively blocking the adsorption sites from a phosphate molecule. Also, the ability of citric acid to mimic the inhibitory effects also suggests that the results of the study are broadly applicable to wetland and other waters with high natural organic acid concentrations.

  4. Evaluation of in vivo and in vitro toxicological and genotoxic potential of aluminum chloride.

    PubMed

    Paz, Letícia Nazareth Fernandes; Moura, Laís Mesquita; Feio, Danielle Cristinne A; Cardoso, Mirella de Souza Gonçalves; Ximenes, Wagner Luiz O; Montenegro, Raquel C; Alves, Ana Paula N; Burbano, Rommel R; Lima, Patrícia Danielle L

    2017-05-01

    Aluminum and its compounds are common contaminants of water and food, as well as medications and cosmetics. The wide distribution of the element facilitates the demand for detailed studies of its biological and toxicological effects. This work aimed to evaluate the possible genotoxic and toxic activity resulting from in vivo and in vitro exposure to Al. For in vivo analysis, 40 Swiss mice were used, various concentrations of hydrated aluminum chloride were administered orally. They were analyzed for possible genic activity and metal cytotoxicity using a micronucleus test (MN), and for toxicity through histopathological evaluation of the extracted organs. For in vitro analysis, lymphocytes from the peripheral blood of 3 healthy donors were used. These cells were exposed to the same chemical agent in various concentrations. In vivo study revealed a significant increase in the number of MN in all Al concentrations. Furthermore, significant alterations in all the organs evaluated were verified by the presence of irreversible lesions (such as necrosis). Corroborating these findings, a significant increase in the quantity of MN in all concentrations with lymphocytes in vitro. In light of this, we suggest that this metal presents genotoxic potential and is potentially a cause of pathological disorders.

  5. Electrophoretic nature and evaluation of poly-aluminum-chloride-sulfate (PACS) as a coagulant for water and wastewater treatment.

    PubMed

    Gao, Bao-yu; Yue, Qin-yan; Wang, Bing-jian

    2003-05-01

    A series of poly-aluminum-chloride-sulfates (PACS), which have different OH/Al (gamma) and Al(3+)/SO4(2-) mole ratios, has been prepared using AlCl3 x 6H2O, A(SO4)3 x 18H2O and Na2CO3 as raw materials. The electrophoretic nature of PACS was investigated by electrophoresis. Laboratory experiments were undertaken to evaluate the PACS in comparison with polyaluminum chloride (PAC) for the coagulation of simulating water and actual wastewaters. The experimental results show that the gamma value and the Al(3+)/SO4(2-) mole ratio affect the electrophoretic nature of PACS. PACS has a maximum zeta potential at about a gamma value of 1.5 and Al(3+)/SO4(2-) mole ratio of 12-16. The zeta potential of PACS varies with pH. The performance of PACS as coagulant is affected by gamma value and Al(3+)/SO4(2-) mole ratio. PACS of gamma = 2.1 and Al(3+)/SO4(2-) = 15 gives best turbidity removal effectiveness. In comparison with PAC of gamma = 2.0, PACS of gamma = 2.0 and Al(3+)/SO4(2-) = 16 gives higher removal efficiency for turbidity and COD, and shows the following advantages in the clarification of waters and wastewaters: rapid aggregation velocity, larger and heavier flocs, and lower required dosage.

  6. Redox flow batteries based on supporting solutions containing chloride

    SciTech Connect

    Li, Liyu; Kim, Soowhan; Yang, Zhenguo; Wang, Wei; Nie, Zimin; Chen, Baowei; Zhang, Jianlu; Xia, Guanguang

    2015-09-01

    Redox flow battery systems having a supporting solution that contains Cl.sup.- ions can exhibit improved performance and characteristics. Furthermore, a supporting solution having mixed SO.sub.4.sup.2- and Cl.sup.- ions can provide increased energy density and improved stability and solubility of one or more of the ionic species in the catholyte and/or anolyte. According to one example, a vanadium-based redox flow battery system is characterized by an anolyte having V.sup.2+ and V.sup.3+ in a supporting solution and a catholyte having V.sup.4+ and V.sup.5+ in a supporting solution. The supporting solution can contain Cl.sup.- ions or a mixture of SO.sub.4.sup.2- and Cl.sup.- ions.

  7. Redox flow batteries based on supporting solutions containing chloride

    SciTech Connect

    Li, Liyu; Kim, Soowhan; Yang, Zhenguo; Wang, Wei; Nie, Zimin; Chen, Baowei; Zhang, Jianlu; Xia, Guanguang

    2015-07-07

    Redox flow battery systems having a supporting solution that contains Cl.sup.- ions can exhibit improved performance and characteristics. Furthermore, a supporting solution having mixed SO.sub.4.sup.2- and Cl.sup.- ions can provide increased energy density and improved stability and solubility of one or more of the ionic species in the catholyte and/or anolyte. According to one example, a vanadium-based redox flow battery system is characterized by an anolyte having V.sup.2+ and V.sup.3+ in a supporting solution and a catholyte having V.sup.4+ and V.sup.5+ in a supporting solution. The supporting solution can contain Cl.sup.- ions or a mixture of SO.sub.4.sup.2- and Cl.sup.- ions.

  8. Redox flow batteries based on supporting solutions containing chloride

    DOEpatents

    Li, Liyu; Kim, Soowhan; Yang, Zhenguo; Wang, Wei; Zhang, Jianlu; Chen, Baowei; Nie, Zimin; Xia, Guanguang

    2014-01-14

    Redox flow battery systems having a supporting solution that contains Cl.sup.- ions can exhibit improved performance and characteristics. Furthermore, a supporting solution having mixed SO.sub.4.sup.2- and Cl.sup.- ions can provide increased energy density and improved stability and solubility of one or more of the ionic species in the catholyte and/or anolyte. According to one example, a vanadium-based redox flow battery system is characterized by an anolyte having V.sup.2+ and V.sup.3+ in a supporting solution and a catholyte having V.sup.4+ and V.sup.5+ in a supporting solution. The supporting solution can contain Cl.sup.- ions or a mixture of SO.sub.4.sup.2- and Cl.sup.- ions.

  9. LOW TEMPERATURE PROCESS FOR THE REMOVAL AND RECOVERY OF CHLORIDES AND NITRATES FROM AQUEOUS NITRATE SOLUTIONS

    DOEpatents

    Savolainen, J.E.

    1963-01-29

    A method is described for reducing the chloride content of a solution derived from the dissolution of a stainless steel clad nuclear fuel element with an aqua regia dissolution medium. The solutlon is adjusted to a nitric acid concentration in the range 5 to 10 M and is countercurrently contacted at room temperature with a gaseous oxide of nitrogen selected from NO, NO/sub 2/, N/sub 2/ O/sub 3/, and N/sub 2/O/sub 4/. Chlo ride is recovered from the contacted solution as nitrosyl chloride. After reduction of the chloride content, the solution is then contacted with gaseous NO to reduce the nitric acid molarity to a desired level. (AEC)

  10. Investigation of the electrodialysis of an aqueous solution of tin(IV) chloride

    SciTech Connect

    Sharygin, L.M.; Zlokazova, E.I.; Shtin, A.P.

    1987-09-20

    The sol-gel method for the synthesis of sorbents on the basis of oxides of polyvalent metals calls for an investigation of the methods for obtaining aqueous sols of oxides of these metals. The purpose of this work was to investigate the polarization of an anion-exchange membrane in solutions of stannic chloride with different concentrations and during electrodialysis, as well as the current efficiency with respect to chlorine, and the transport numbers of the chloride ion as a function of the current density and the temperature. The polarization curves recorded for an MA-41L membrane in dilute solutions of tin(IV) chloride tended to show an increase in the limiting current in comparison to the case of hydrochloric acid with the same electrical conductivity owing to the ion-exchange properties of the colloidal particles of hydrated tin dioxide formed during the hydrolysis and polymerization of tin in solution.

  11. Effect of metal chloride solutions on coloration and biaxial flexural strength of yttria-stabilized zirconia

    NASA Astrophysics Data System (ADS)

    Oh, Gye-Jeong; Lee, Kwangmin; Lee, Doh-Jae; Lim, Hyun-Pil; Yun, Kwi-Dug; Ban, Jae-Sam; Lee, Kyung-Ku; Fisher, John G.; Park, Sang-Won

    2012-10-01

    The effect of three kinds of transition metal dopants on the color and biaxial flexural strength of zirconia ceramics for dental applications was evaluated. Presintered zirconia discs were colored through immersion in aqueous chromium, molybdenum and vanadium chloride solutions and then sintered at 1450 °C. The color of the doped specimens was measured using a digital spectrophotometer. For biaxial flexural strength measurements, specimens infiltrated with 0.3 wt% of each aqueous chloride solution were used. Uncolored discs were used as a control. Zirconia specimens infiltrated with chromium, molybdenum and vanadium chloride solutions were dark brown, light yellow and dark yellow, respectively. CIE L*, a*, and b* values of all the chromium-doped specimens and the specimens infiltrated with 0.1 wt% molybdenum chloride solution were in the range of values for natural teeth. The biaxial flexural strengths of the three kinds of metal chloride groups were similar to the uncolored group. These results suggest that chromium and molybdenum dopants can be used as colorants to fabricate tooth colored zirconia ceramic restorations.

  12. Recycling of aluminum and caustic soda solution from waste effluents generated during the cleaning of the extruder matrixes of the aluminum industry.

    PubMed

    Tansens, Pieter; Rodal, Alberto T; Machado, Carina M M; Soares, Helena M V M

    2011-03-15

    Anodising industries use a concentrated caustic soda solution to remove aluminum from extruder matrixes. This procedure produces very alkaline effluents containing high amounts of aluminum. The work reported here was focussed on recycling aluminum, as aluminum hydroxide, from these effluents and regenerating an alkaline sodium hydroxide solution. Briefly, the method comprises a dilution step (necessary for reducing the viscosity of the effluent and allowing the subsequent filtration) followed by a filtration to eliminate a substantial amount of the insoluble iron. Then, sulphuric acid was added to neutralize the waste solution down to pH 12 and induce aluminum precipitation. The purity of the aluminum salt was improved after washing the precipitate with deionised water. The characterization of the solid recovered, performed by thermogravimetric analysis, Fourier transform infrared spectroscopy and X-ray diffraction, indicated characteristics typical of bayerite. The proposal method allowed recovering 82% of the aluminum present in the wastewater with high purity (99.5%). Additionally, a sufficiently concentrated caustic soda solution was also recovered, which can be reused in the anodising industries. This procedure can be easily implemented and ensures economy by recycling reagents (concentrated caustic soda solution) and by recovering commercial by-products (aluminum hydroxide), while avoiding environmental pollution.

  13. Leaching of diethylhexyl phthalate from polyvinyl chloride bags into intravenous cyclosporine solution

    SciTech Connect

    Venkataramanan, R.; Burckart, G.J.; Ptachcinski, R.J.; Blaha, R.; Logue, L.W.; Bahnson, A.; Giam, C.S.; Brady, J.E.

    1986-11-01

    The release of diethylhexyl phthalate (DEHP) from flexible polyvinyl chloride containers into intravenous cyclosporine solutions was studied. Intravenous cyclosporine solution or solutions containing the vehicle Cremophor EL and alcohol in dextrose were prepared in an all-glass system and stored in polyvinyl chloride (PVC) bags. Four samples were obtained at different time intervals, and DEHP content was analyzed by gas chromatography. The amount of DEHP that was leached into solutions stored in the PVC bags increased as storage time increased. By 48 hours, nearly 33 mg of DEHP had leached into the solution. Intravenous cyclosporine solutions should be prepared in glass containers to minimize patient exposure to DEHP. If plastic bags are used for preparing cyclosporine injections, the injections must be used immediately after preparation.

  14. Fabrication and Performance of All-Solid-State Chloride Sensors in Synthetic Concrete Pore Solutions

    PubMed Central

    Gao, Xiaojian; Zhang, Jian; Yang, Yingzi; Deng, Hongwei

    2010-01-01

    One type of all-solid-state chloride sensor was fabricated using a MnO2 electrode and a Ag/AgCl electrode. The potentiometric response of the sensor to chloride in synthetic concrete pore solutions was systematically studied, and the polarization performance was also evaluated. The results show a good linear relationship between the potential reading of the sensor and the logarithm of chloride activity (concentration ranges from 0.05 to 5.0 M), and the potential value remains stable with increasing immersion time. The existence of K+, Ca2+, Na+ and SO42− ions have little influence on the potentiometric response of the sensor to chloride, but the pH has a significant influence on the potential value of the sensor at low chloride concentration. The potential reading of the sensor increases linearly with the solution temperature over the range from 5 to 45 °C. Meanwhile, an excellent polarization behavior is proven by galvanostatic and potentiodynamic tests. All of the results reveal that the developed sensor has a great potential for monitoring chloride ions in concrete environments. PMID:22163467

  15. Zinc chloride aqueous solution as a solvent for starch.

    PubMed

    Lin, Meiying; Shang, Xiaoqin; Liu, Peng; Xie, Fengwei; Chen, Xiaodong; Sun, Yongyi; Wan, Junyan

    2016-01-20

    It is important to obtain starch-based homogeneous systems for starch modification. Regarding this, an important key point is to find cheap, low-cost and low-toxicity solvents to allow complete dissolution of starch and its easy regeneration. This study reveals that a ZnCl2 aqueous solution is a good non-derivatizing solvent for starch at 50 °C, and can completely dissolve starch granules. The possible formation of a "zinc-starch complex" might account for the dissolution; and the degradation of starch, which was caused by the H(+) inZnCl2 aqueous solution, could not contribute to full dissolution. From polarized light microscopic observation combined with the solution turbidity results, it was found that the lowest ZnCl2 concentration for full dissolution was 29.6 wt.% at 50 °C, with the dissolving time being 4h. Using Fourier-transform infrared (FTIR), solid state (13)C nuclear magnetic resonance (NMR), and X-ray diffraction (XRD), it was revealed that ZnCl2 solution had no chemical reaction with starch glucosides, but only weakened starch hydrogen bonding and converted the crystalline regions to amorphous regions. In addition, as shown by intrinsic viscosity and thermogravimetric analysis (TGA), ZnCl2 solution caused degradation of starch macromolecules, which was more serious with a higher concentration of ZnCl2 solution.

  16. Effect of aging on aluminum hydroxide complexes in dilute aqueous solutions

    USGS Publications Warehouse

    Smith, Ross Wilbert; Hem, John David

    1972-01-01

    Aqueous aluminum solutions containing 4?10 -5 mole/liter aluminum and a constant total ionic strength of 10 -2, but with varying ratios of hydroxide to aluminum (OH:Al), were prepared. Progress of these solutions toward equilibrium conditions over aging periods of as much as 2 years was studied by determining the composition and pH of the solutions at various time intervals. The solutions, after mixing, were supersaturated with respect to both crystalline and amorphous forms of aluminum oxides and aluminum hydroxides. The compositions of the solutions were determined by use of a timed colorimetric analytical procedure which allowed the estimation of three separate forms of aluminum that have been designated Al a, Al b, and Al c. Form Al a appeared to be composed of monomeric species such as Al(H20)6+3, Al(OH)(H20)5+2, Al(OH)2(H20)4 +I and Al(OH)4-. Form Al b was polynuclear material containing perhaps 20-400 aluminum atoms per structure. It appeared to be a metastable material. Form Al c was composed of relatively large, microcrystalline, clearly solid AI(OH)3 particles. For each OH :Al ratio, the concentration of Al a remained constant with aging time, Al b decreased, and Al c increased. It appeared that Al b particles were increasing in size and ultimately were converted to Al c particles. After a few weeks' aging, Al c particles had the structure of gibbsite. In all solutions, equilibrium was only very slowly achieved, and the time required depended on the OH:Al ratio and how rapidly the solution was initially prepared (mixing time). Lower ratios caused a slower approach to equilibrium; sometimes equilibrium was not achieved even after several years' aging. The more slowly base was initially added (to obtain the proper OH:Al ratio), the more slowly was equilibrium approached. Ultimate equilibrium values of dissolved aluminum concentration and pH were consistent with known thermodynamic data on monomeric aluminum species. From data determined during the aging

  17. Nucleation and growth of zinc from chloride concentrated solutions

    SciTech Connect

    Trejo, G.; Ortega B, R.; Meas V, Y.; Ozil, P.; Chainet, E.; Nguyen, B.

    1998-12-01

    The electrodeposition of metals is a complex phenomenon influenced by a number of factors that modify the rates of nucleation and growth and determine the properties of the deposits. In this work the authors study the influence of the zinc chloride (ZnCl{sub 2}) concentration on the zinc nucleation process on glassy carbon, in a KCl electrolyte under conditions close to those employed in commercial acid deposition baths for zinc. The electrochemical study was performed using cyclic voltammetry and potentiostatic current-time transients. The charge-transfer coefficient and the formal potential for ZnCl{sub 2} reduction were evaluated from cyclic voltammetry experiments. The nucleation process was analyzed by comparing the transients obtained with the known dimensionless (i/i{sub m}){sup 2} vs. t/t{sub m} response for instantaneous or progressive nucleation. The results show that the nucleation process and the number density of sites are dependent on ZnCl{sub 2} concentration. Scanning electron microscopy analysis of the deposits shows that the deposits are homogeneous and compact although a change in the morphology is observed as a function of ZnCl{sub 2} concentration. Evaluation of the corrosion resistance reveals the influence of the nucleation process on the subsequent corrosion resistance of the zinc deposits.

  18. Solute rejection by porous glass membranes. I - Hyperfiltration of sodium chloride and urea feed solutions.

    NASA Technical Reports Server (NTRS)

    Ballou, E. V.; Wydeven, T.; Leban, M. I.

    1971-01-01

    Hyperfiltration of sodium chloride and urea was studied with porous glass membranes in closed-end capillary form, to determine the effect of pressure, temperature, and concentration variations, and lifetime rejection and flux characteristics. Rejection data for sodium chloride were consistent with the functioning of the porous glass as a low-capacity ion-exchange membrane.

  19. Effect of Sodium Chloride on the Surface and Wetting Properties of Aqueous Solutions of Cocamidopropyl Betaine.

    PubMed

    Staszak, Katarzyna; Wieczorek, Daria; Michocka, Katarzyna

    Surfactants are important ingredients of personal care products and household products. The main characteristic of these compounds is to decrease the surface tension of solvent and resulting many properties such as contact angle, foam properties etc. The coexistence of other ingredients in the product may affect the properties of surfactants. One of the main components contained in almost every personal care and household product is sodium chloride. The main aim of this work was to determine the effect of this salt on some surface and usage properties of cocamidopropyl betaine (CAPB). From our experiments it was shown that the effect of added sodium chloride in the aqueous solutions of CAPB on the properties is the opposite to the one described in the literature for cationic and anionic surfactants, i.e., CMC increases with increasing ionic strength, foam height decreases with increasing salt concentration. Our investigation showed that sodium chloride makes worse the properties of the CAPB solutions examined in this work.

  20. Corrosion resistance of flaky aluminum pigment coated with cerium oxides/hydroxides in chloride and acidic electrolytes

    NASA Astrophysics Data System (ADS)

    Niroumandrad, S.; Rostami, M.; Ramezanzadeh, B.

    2015-12-01

    The objective of this study was to enhance the corrosion resistance of lamellar aluminum pigment through surface treatment by cerium oxides/hydroxides. The surface composition of the pigments was studied by energy-dispersive spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). The corrosion resistance of the pigment was evaluated by conventional hydrogen evolution measurements in acidic solution and electrochemical impedance spectroscopy (EIS) in 3.5% NaCl solution. Results showed that the Ce-rich coating composed of Ce2O3 and CeO2 was precipitated on the pigment surface after immersion in the cerium solution. The corrosion resistance of pigment was significantly enhanced after modification with cerium layer.

  1. Stability of Melphalan in 0.9% Sodium Chloride Solutions Prepared in Polyvinyl Chloride Bags for Intravenous Injection.

    PubMed

    Desmaris, Romain-Pacôme; Mercier, Lionel; Paci, Angelo

    2015-09-01

    Melphalan is an alkylating agent frequently used in an intravenous formulation to treat hematologic malignancies and solid tumors in both adults and children. According to the manufacturer, melphalan is stable in sterile 0.9% sodium chloride for 90 min at room temperature (RT). Several authors have studied the stability of different concentrations of melphalan; however, most were not adapted to the current manufacturing process applied in pharmaceutical centralized units. This study was conducted to determine the stability of melphalan in 0.9% sodium chloride solutions at concentrations used for intravenous injection in practice. Melphalan is commonly prepared in diluted solutions ranging from 2 to 4 mg/ml for the treatment of adult patients and at lower concentrations (down to 0.5 mg/ml) for pediatric use. Accordingly, these were the three concentrations chosen for this study. Melphalan concentrations were measured with high-performance thin-layer chromatography (HPTLC). At RT, admixtures prepared at 4 mg/ml were stable for up to 8 h without protection from light; however, at lower concentrations, such as 0.5 and 2 mg/ml, stability did not exceed 2 h. When refrigerated, melphalan was stable for 24 h at 2 mg/ml; however, at 0.5 and 4 mg/ml, the drug was not stable. Melphalan solutions present with limited stability at 0.5, 2, and 4 mg/ml and are not adapted for delayed administration in pharmaceutical centralized units. However, at 4 mg/ml and at RT, a stability of 8 h is very interesting in practice and allows sufficient time for preparation, pharmaceutical control, transport, and administration.

  2. Experimental study of directional solidification of aqueous ammonium chloride solution

    NASA Technical Reports Server (NTRS)

    Chen, C. F.; Chen, Falin

    1991-01-01

    Directional solidification experiments have been carried out using the analog casting system of NH4Cl-H2O solution by cooling it from below with a constant-temperature surface ranging from -31.5 C to +11.9 C. The NH4Cl concentration was 26 percent in all solutions, with a liquidus temperature of 15 C. It was found that finger convection occurred in the fluid region just above the mushy layer in all experiments. Plume convection with associated chimneys in the mush occurred in experiments with bottom temperatures as high as +11.0 C. However, when the bottom temperature was raised to +11.9 C, no plume convection was observed, although finger convection continued as usual. A method has been devised to determine the porosity of the mush by computed tomography. Using the mean value of the porosity across the mush layer and the permeability calculated by the Kozeny-Carman relationship, the critical solute Rayleigh number across the mush layer for onset of plume convection was estimated to be between 200 and 250.

  3. Electrochemical Evaluation of Stainless Steels in Acidified Sodium Chloride Solutions

    NASA Technical Reports Server (NTRS)

    Calle, L. M.; MacDowell, L. G.; Vinje, R. D.

    2004-01-01

    This paper presents the results of an investigation in which several 300-series stainless steels (SS): AISI S30403 SS (UNS S30403), AISI 316L SS (UNS S31603), and AISI 317L SS (LINS S31703), as well as highly-alloyed: SS 254-SMO (UNS S32154), AL-6XN (N08367) and AL29-4C (UNS S44735), were evaluated using DC electrochemical techniques in three different electrolyte solutions. The solutions consisted of neutral 3.55% NaCl, 3.55% NaCl in 0.1N HCl, and 3.55% NaCl in 1.0N HCl. These solutions were chosen to simulate environments that are less, similar, and more aggressive, respectively, than the conditions at the Space Shuttle launch pads. The electrochemical test results were compared to atmospheric exposure data and evaluated for their ability to predict the long-term corrosion performance of the subject alloys. The electrochemical measurements for the six alloys indicated that the higher-alloyed SS 254-SMO, AL29-4C, and AL-6XN exhibited significantly higher resistance to localized corrosion than the 300-series SS. There was a correlation between the corrosion performance of the alloys during a two-year atmospheric exposure and the corrosion rates calculated from electrochemical (polarization resistance) measurements.

  4. Dissolution of Oxide Films on Aluminum in Near Neutral Solutions

    SciTech Connect

    Isaacs, Hugh S.; Xu, Feng; Jeffcoate, Carrol S.

    1999-10-17

    Simple linear potentiodynamic cycling measurements have been made on abraded pure Al in borate, chromate, phosphate, sulfate and nitrate solutions. In borate and chromate solutions the currents continued to decrease with each subsequent cycle. In phosphate dissolution of the oxide takes place producing repetitive repeat curves. The current variations in borate and chromate were simulated using a high field conduction oxide growth model. Including oxide dissolution in the model simulated the phosphate behavior. Results in sulfate and nitrate solutions were more complex. The behavior in the sulfate solution was attributed to effects of sulfate the oxide/solution interface.

  5. Lidocaine stability in cardioplegic solution stored in glass bottles and polyvinyl chloride bags.

    PubMed

    Lackner, T E; Baldus, D; Butler, C D; Amyx, C; Kessler, G

    1983-01-01

    The stability of lidocaine hydrochloride in buffered cardioplegic solutions stored in glass and polyvinyl chloride bags was studied. Concentrations of lidocaine (incorporated as the hydrochloride salt) were measured in buffered cardioplegic solutions containing potassium chloride, sodium bicarbonate, dextrose, and sodium chloride. Solutions were stored at 22 +/- 2 degrees C and 4 degrees C in glass bottles and 500-ml and 250-ml polyvinyl chloride (PVC) containers; some 250-ml PVC bags were underfilled to study the effects of varying surface area-volume ratios. Lidocaine concentrations were measured using a homogeneous enzyme immunoassay (EMIT, Syva Corporation) on days 0, 1, 2, 7, and 21. Lidocaine concentrations decreased significantly in all PVC bags stored at 22 degrees C and in underfilled PVC bags stored at 4 degrees C. Lidocaine loss in PVC bags appeared to result from sorption. It is concluded that lidocaine is stable in cardioplegic solutions when these are refrigerated and stored in glass containers or filled large-volume PVC bags for 21 days.

  6. Sodium chloride methanol solution spin-coating process for bulk-heterojunction polymer solar cells

    NASA Astrophysics Data System (ADS)

    Liu, Tong-Fang; Hu, Yu-Feng; Deng, Zhen-Bo; Li, Xiong; Zhu, Li-Jie; Wang, Yue; Lv, Long-Feng; Wang, Tie-Ning; Lou, Zhi-Dong; Hou, Yan-Bing; Teng, Feng

    2016-08-01

    The sodium chloride methanol solution process is conducted on the conventional poly(3-hexylthiophene) (P3HT)/[6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) polymer bulk heterojunction solar cells. The device exhibits a power conversion efficiency of up to 3.36%, 18% higher than that of the device without the solution process. The measurements of the active layer by x-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and ultraviolet photoelectron spectroscopy (UPS) indicate a slight phase separation in the vertical direction and a sodium chloride distributed island-like interface between the active layer and the cathode. The capacitance-voltage (C-V) and impedance spectroscopy measurements prove that the sodium chloride methanol process can reduce the electron injection barrier and improve the interfacial contact of polymer solar cells. Therefore, this one-step solution process not only optimizes the phase separation in the active layers but also forms a cathode buffer layer, which can enhance the generation, transport, and collection of photogenerated charge carriers in the device simultaneously. This work indicates that the inexpensive and non-toxic sodium chloride methanol solution process is an efficient one-step method for the low cost manufacturing of polymer solar cells. Project supported by the Fundamental Research Funds for the Central Universities, China (Grant No. 2014JBZ009) and the National Natural Science Foundation of China (Grant Nos. 61274063, 61377028, 61475014, and 61475017).

  7. The optical constants of several atmospheric aerosol species - Ammonium sulfate, aluminum oxide, and sodium chloride

    NASA Technical Reports Server (NTRS)

    Toon, O. B.; Pollack, J. B.; Khare, B. N.

    1976-01-01

    An investigation is conducted of problems which are related to a use of measured optical constants in the simulation of the optical constants of real atmospheric aerosols. The techniques of measuring optical constants are discussed, taking into account transmission measurements through homogeneous and inhomogeneous materials, the immersion of a material in a liquid of a known refractive index, the consideration of the minimum deviation angle of prism measurement, the interference of multiply reflected light, reflectivity measurements, and aspects of mathematical analysis. Graphs show the real and the imaginary part of the refractive index as a function of wavelength for aluminum oxide, NaCl, and ammonium sulfate. Tables are provided for the dispersion parameters and the optical constants.

  8. Removal of hydrogen chloride from gaseous streams using magnesium-aluminum oxide.

    PubMed

    Kameda, Tomohito; Uchiyama, Naoya; Park, Kye-Sung; Grause, Guido; Yoshioka, Toshiaki

    2008-10-01

    Magnesium-aluminum oxide (Mg-Al oxide) obtained by thermal decomposition of Mg-Al layered double hydroxide (Mg-Al LDH) effectively removed HCl from gaseous streams. HCl removal was greater in the presence of added water vapor at all temperatures examined and increased with decreasing temperature in both the presence and absence of added water vapor. Wet and dry removal of gaseous HCl were attributed to the production of MgCl2 . 6H2O and MgCl2 . 4H2O, respectively. For the wet scrubbing process, the reconstruction reaction of Mg-Al LDH from Mg-Al oxide was the primary mechanism for increased HCl removal.

  9. Interactions between hydrophobic and ionic solutes in aqueous guanidinium chloride and urea solutions: lessons for protein denaturation mechanism.

    PubMed

    O'Brien, Edward P; Dima, Ruxandra I; Brooks, Bernard; Thirumalai, D

    2007-06-13

    In order to clarify the mechanism of denaturant-induced unfolding of proteins we have calculated the interactions between hydrophobic and ionic species in aqueous guanidinium chloride and urea solutions using molecular dynamics simulations. Hydrophobic association is not significantly changed in urea or guanidinium chloride solutions. The strength of interaction between ion pairs is greatly diminished by the guanidinium ion. Although the changes in electrostatic interactions in urea are small, examination of structures, using appropriate pair functions, of urea and water around the solutes show strong hydrogen bonding between urea's carbonyl oxygen and the positively charged solute. Our results strongly suggest protein denaturation occurs by the direct interaction model according to which the most commonly used denaturants unfold proteins by altering electrostatic interactions either by solvating the charged residues or by engaging in hydrogen bonds with the protein backbone. To further validate the direct interaction model we show that, in urea and guanidinium chloride solutions, unfolding of an unusually stable helix (H1) from mouse PrPC (residues 144-153) occurs by hydrogen bonding of denaturants to charged side chains and backbone carbonyl groups.

  10. Investigations of Selective Interactions of the Iron/Aqueous Sodium Chloride System. Part 1. The Adsorption of Chloride Ion by Alpha-Iron(III) Oxide in Sodium Chloride Solutions Saturated by Oxygen at 30C

    DTIC Science & Technology

    A radioisotope procedure was used to investigate the chloride ion adsorption characteristics of crystalline alpha - iron (III) oxide in dilute sodium...competed for the active sites on hydrated alpha - iron (III) oxide surfaces. The chloride ion was preferentially adsorbed in the solution pH range of

  11. Aluminum contamination of parenteral nutrition additives, amino acid solutions, and lipid emulsions.

    PubMed

    Popińska, K; Kierkuś, J; Lyszkowska, M; Socha, J; Pietraszek, E; Kmiotek, W; Ksiazyk, J

    1999-09-01

    Contamination of parenteral nutrition solutions with aluminum may result in accumulation of this element in bones and, in premature infants, may inhibit bone calcium uptake and induce cholestasis. We measured the aluminum concentration of small-volume parenterals, amino acid solutions, lipid emulsions, and special solutions containing glucose, amino acids, electrolytes, and trace elements (standard I for children with a body weight of 3-5 kg, standard II for children with a body weight of 5-10 kg). The method used was graphite furnace atomic absorption spectrometry GTA-AAS (SpectrAA-400 Plus, Varian, PtY Ltd., Mulgrave, Australia). Quality control was run with the use of control serum (Seronorm, Nycomed, Oslo, Norway). The aluminum contents of parenterally administered solutions were: pediatric trace elements, 130 micrograms/L, and pediatric trace elements, 3000 micrograms/L; phosphorus salts: K-phosphates, 9800 micrograms/L, and Na/K phosphates, 13,000 micrograms/L; 10% calcium gluconate, 4400 micrograms/L; 6.5% amino acids, 30 micrograms/L; 10% amino acids, 120 micrograms/L; 12.5% amino acids, 121 micrograms/L; 20% lipid emulsion, 30 micrograms/L; 20% lipid emulsion, 180 micrograms/L; water-soluble vitamins, 12 micrograms/L; lipid soluble vitamins, 360 micrograms/L; standard I, 55 micrograms/L; standard II, 90 micrograms/L; The aluminum intake from parenteral nutrition was 6.6-10.8 micrograms.kg-1.d-1--a dose exceeding the safety limit of 2 micrograms.kg-1.d-1. The possible association of aluminum not only with metabolic bone disease, but also with encephalopathy, dictates caution when dealing with the pediatric population on long-term parenteral nutrition. In the absence of reliable label information, it seems proper to monitor the aluminum concentration in parenteral nutrition products and to report it in professional journals.

  12. The simultaneous removal of calcium, magnesium and chloride ions from industrial wastewater using magnesium-aluminum oxide.

    PubMed

    Hamidi, Roya; Kahforoushan, Davood; Fatehifar, Esmaeil

    2013-01-01

    In this article, a method for simultaneous removal of calcium, magnesium and chloride by using Mg0.80Al0.20O1.10 as a Magnesium-Aluminum oxide (Mg‒Al oxide) was investigated. Mg‒Al oxide obtained by thermal decomposition of the Mg-Al layered double hydroxide (Mg-Al LDH). The synthesized Mg‒Al oxide were characterized with respect to nitrogen physicosorption, X-ray diffraction (XRD) and field emission scan electron microscopy (FESEM) morphology. Due to high anion-exchange capacity of Mg‒Al oxide, it was employed in simultaneously removal of Cl(-), Mg(+2) and Ca(+2) from distiller waste of a sodium carbonate production factory. For this purpose, experiments were designed to evaluate the effects of quantity of Mg‒Al oxide, temperature and time on the removal process. The removal of Cl(-), Mg(+2) and Ca(+2) from wastewater was found 93.9%, 93.74% and 93.25% at 60°C after 0.5 h, respectively. Results showed that the removal of Cl(-), Mg(+2) and Ca(+2) by Mg‒Al oxide increased with increasing temperature, time and Mg‒Al oxide quantity.

  13. Photodynamic inactivation of planktonic cultures and biofilms of Candida albicans mediated by aluminum-chloride-phthalocyanine entrapped in nanoemulsions.

    PubMed

    Ribeiro, Ana Paula Dias; Andrade, Mariana Carvalho; da Silva, Julhiany de Fátima; Jorge, Janaina Habib; Primo, Fernando Lucas; Tedesco, Antonio Cláudio; Pavarina, Ana Cláudia

    2013-01-01

    New drug delivery systems, such as nanoemulsions (NE), have been developed to allow the use of hydrophobic drugs on the antimicrobial photodynamic therapy. This study evaluated the photodynamic potential of aluminum-chloride-phthalocyanine (ClAlPc) entrapped in cationic and anionic NE to inactivate Candida albicans planktonic cultures and biofilm compared with free ClAlPc. Fungal suspensions were treated with different delivery systems containing ClAlPc and light emitting diode. For planktonic suspensions, colonies were counted and cell metabolism was evaluated by XTT assay. Flow cytometry evaluated cell membrane damage. For biofilms, the metabolic activity was evaluated by XTT and ClAlPc distribution through biofilms was analyzed by confocal laser scanning microscopy (CLSM). Fungal viability was dependent on the delivery system, superficial charge and light dose. Free ClAlPc caused photokilling of the yeast when combined with 100 J cm(-2). Cationic NE-ClAlPc reduced significantly both colony counts and cell metabolism (P < 0.05). In addition, cationic NE-ClAlPc and free ClAlPc caused significant damage to the cell membrane (P < 0.05). For the biofilms, cationic NE-ClAlPc reduced cell metabolism by 70%. Anionic NE-ClAlPc did not present antifungal activity. CLSM showed different accumulation on biofilms between the delivery systems. Although NE system showed a lower activity for planktonic culture, cationic NE-ClAlPc showed better results for Candida biofilms.

  14. Effects of aluminum chloride-catalyzed hydrothermal pretreatment on the structural characteristics of lignin and enzymatic hydrolysis.

    PubMed

    Shen, Xiao-Jun; Wang, Bing; Huang, Pan-Li; Wen, Jia-Long; Sun, Run-Cang

    2016-04-01

    In this study, Eucalyptus camaldulensis was pretreated with 0.02 M aluminum chloride (AlCl3) at 140-180 °C to obtain digestible substrates for glucose and lignin. The effects of AlCl3-catalyzed hydrothermal pretreatment on the degradation of carbohydrates, structural changes of lignin, crystallinity, morphologic changes, and cellulose conversion of the pretreated biomass have been investigated by HAPEC, HPLC, FT-IR, XRD, CP/MAS NMR, SEM, and 2D-HSQC NMR. Results showed that the pretreatment significantly removed hemicelluloses and cleaved β-O-4 linkages of lignin at high temperatures. Under an optimum condition (at 170 °C for 1 h), almost all of hemicelluloses were removed and most of β-O-4 linkages in lignin were cleaved, and 77.8% cellulose conversion of the pretreated biomass was achieved, which was 7.3-fold higher than that of the original biomass. In short, this process was regarded as a promising approach to achieve an efficient conversion of lignocellulosic biomass to fermentable glucose and residual lignin.

  15. Aluminum chloride induces neuroinflammation, loss of neuronal dendritic spine and cognition impairment in developing rat.

    PubMed

    Cao, Zheng; Yang, Xu; Zhang, Haiyang; Wang, Haoran; Huang, Wanyue; Xu, Feibo; Zhuang, Cuicui; Wang, Xiaoguang; Li, Yanfei

    2016-05-01

    Aluminum (Al) is present in the daily life of humans, and the incidence of Al contamination increased in recent years. Long-term excessive Al intake induces neuroinflammation and cognition impairment. Neuroinflammation alter density of dendritic spine, which, in turn, influence cognition function. However, it is unknown whether increased neuroinflammation is associated with altered density of dendritic spine in Al-treated rats. In the present study, AlCl3 was orally administrated to rat at 50, 150 and 450 mg/kg for 90d. We examined the effects of AlCl3 on the cognition function, density of dendritic spine in hippocampus of CA1 and DG region and the mRNA levels of IL-1β, IL-6, TNF-α, MHC II, CX3CL1 and BNDF in developing rat. These results showed exposure to AlCl3 lead to increased mRNA levels of IL-1β, IL-6, TNF-α and MCH II, decreased mRNA levels of CX3CL1 and BDNF, decreased density of dendritic spine and impaired learning and memory in developing rat. Our results suggest AlCl3 can induce neuroinflammation that may result in loss of spine, and thereby leads to learning and memory deficits.

  16. Towards an understanding of solvent extraction--electroanalytical characterization of chloride-leaching solutions.

    PubMed

    Paiva, A P; Abrantes, L M

    2001-08-01

    Solvent extraction has been employed to purify media simulating chloride-leaching solutions resulting from complex sulfide concentrate processing, and cyclic voltammetry (CV) has been chosen to characterize those hydrometallurgical aqueous phases. The possibilities of the CV technique were investigated by the evaluation of the adequacy of a specific organic extractant, triisobutylphosphine sulfide, aimed to efficiently and selectively extract silver from a complex chloride medium, additionally containing tenfold to 40-fold molar concentrations of iron, copper and lead. The influence of the oxidation state of the metallic ions present in the feed solution, namely Cu(II) and Cu(I), is considered. The possibilities of CV analysis for the characterization of stripping solutions are also illustrated.

  17. Fourteen-year survival of Pseudomonas cepacia in a salts solution preserved with benzalkonium chloride.

    PubMed Central

    Geftic, S G; Heymann, H; Adair, F W

    1979-01-01

    A strain of Pseudomonas cepacia that survived for 14 years (1963 to 1977) as a contaminant in an inorganic salt solution which contained commercial 0.05% benzalkonium chloride (CBC) as an antimicrobial preservative, was compared to a recent clinical isolate of P. cepacia. Ammonium acetate was present in the concentrated stock CBC solution, and served as a carbon and nitrogen source for growth when carried over into the salts solution with the CBC. The isolate's resistance to pure benzalkonium chloride was increased step-wise to a concentration of 16%. Plate counts showed 4 x 10(3) colony-forming units per ml in the salts solution. Comparison of growth rates, mouse virulence, antibiotics resistance spectra, and substrate requirements disclosed no differences between the contaminant and a recently isolated clinical strain of P. cepacia. The results indicate that it is critical that pharmaceutical solutions containing benzalkonium chloride as an antimicrobial preservative be formulated without extraneous carbon and nitrogen sources or be preserved with additional antimicrobial agents. PMID:453827

  18. Spectroscopic analysis of aluminum chloride phthalocyanine in binary water/ethanol systems for the design of a new drug delivery system for photodynamic therapy cancer treatment

    NASA Astrophysics Data System (ADS)

    Jayme, Cristiano Ceron; Calori, Italo Rodrigo; Tedesco, Antonio Claudio

    2016-01-01

    This study evaluated the behavior of aluminum chloride phthalocyanine in a binary water/ethanol mixture using electronic absorption spectroscopy and static and time-resolved fluorescence spectroscopy. The electronic absorption spectra, resonance light scattering and fluorescence quenching of aluminum chloride phthalocyanine in water/ethanol mixtures were studied at several concentrations. The electronic absorption spectra and fluorescence quenching changed significantly at approximately 50% water (v/v). Below 50% water, the dimerization constant values were negative (- 2609.2 M- 1 and - 506.5 M- 1 at 30% and 40% of water, respectively), indicating that the formation of aggregates under these conditions is not favored. However, at 50% water, the dimerization constant value was estimated to be 559.7 M- 1, which indicates the presence of dimers. Above 60% water, the aggregation process was responsible for the balance between large complexes (such as trimers, tetramers or oligomers) formed in the medium under these conditions. The appearance of new absorption bands at 387 nm and 802 nm and their bathochromic shift relative to the monomer bands suggested that some J-type aggregates form. These results are relevant to understanding the behavior and use of aluminum chloride phthalocyanine in the design of new drug delivery systems for clinical application in photodynamic therapy as a new approach to treat skin cancer.

  19. Spectroscopic analysis of aluminum chloride phthalocyanine in binary water/ethanol systems for the design of a new drug delivery system for photodynamic therapy cancer treatment.

    PubMed

    Jayme, Cristiano Ceron; Calori, Italo Rodrigo; Tedesco, Antonio Claudio

    2016-01-15

    This study evaluated the behavior of aluminum chloride phthalocyanine in a binary water/ethanol mixture using electronic absorption spectroscopy and static and time-resolved fluorescence spectroscopy. The electronic absorption spectra, resonance light scattering and fluorescence quenching of aluminum chloride phthalocyanine in water/ethanol mixtures were studied at several concentrations. The electronic absorption spectra and fluorescence quenching changed significantly at approximately 50% water (v/v). Below 50% water, the dimerization constant values were negative (-2609.2 M(-1) and -506.5 M(-1) at 30% and 40% of water, respectively), indicating that the formation of aggregates under these conditions is not favored. However, at 50% water, the dimerization constant value was estimated to be 559.7 M(-1), which indicates the presence of dimers. Above 60% water, the aggregation process was responsible for the balance between large complexes (such as trimers, tetramers or oligomers) formed in the medium under these conditions. The appearance of new absorption bands at 387 nm and 802 nm and their bathochromic shift relative to the monomer bands suggested that some J-type aggregates form. These results are relevant to understanding the behavior and use of aluminum chloride phthalocyanine in the design of new drug delivery systems for clinical application in photodynamic therapy as a new approach to treat skin cancer.

  20. Respiratory symptoms among glass bottle makers exposed to stannic chloride solution and other potentially hazardous substances

    SciTech Connect

    Levy, B.S.; Davis, F.; Johnson, B.

    1985-04-01

    Concern about upper respiratory tract irritation and other symptoms among workers at a glass bottle manufacturing plant led to an epidemiologic and an industrial hygiene survey. Questionnaire responses from 35 hot end and 53 cold end workers indicated that the incidence of wheezing, chest pain, dyspnea on exertion, and cough was significantly elevated among hot end workers. Among both smokers and nonsmokers, hot end workers reported higher, but not significantly higher, rates of wheezing and chest pain. Among smokers, hot end workers reported significantly higher rates of dyspnea on exertion and cough than did cold end workers. Data suggest that reported exposure to stannic chloride solution likely caused these symptoms. The industrial hygiene survey, conducted when stannic chloride use had been reduced, cleaning had been done, and ventilation improved, focused on measuring air contaminants that might possibly cause symptoms. Levels of hydrogen chloride, which apparently was formed by the combination of stannic chloride and water in the presence of heat, were elevated. The finding of increased prevalence of respiratory symptoms among hot end workers was consistent with this exposure. Recommendations were made to reduce hazardous exposures at this plant. Individuals responsible for occupational health should be aware that relatively benign substances, such as stannic chloride and water, can combine spontaneously to form hazardous substances.

  1. Removal of arsenic(III) and arsenic(IV) ions from aqueous solutions with lanthanum(III) salt and comparison with aluminum(III), calcium(II), and iron(III) salts

    SciTech Connect

    Tokunaga, S.; Yokoyama, S.; Wasay, S.A.

    1999-05-01

    Interactions of arsenic(III) and arsenic(V) ions with a lanthanum salt were studied with the aim of developing a new precipitation method for removal of arsenic from aqueous solutions. Performance was compared to those of aluminum, polyaluminum chloride (PAC), calcium, and iron(III) salts. Arsenic(III) was removed by iron(III) and lanthanum in a narrow pH range with less than 605 removal. Arsenic(V) was removed more efficiently by aluminum, PAC, iron(III), and lanthanum. Lanthanum was most effective, meeting Japanese effluent and drinking water standards by adding three times as much lanthanum as arsenic(V).

  2. Concentrations of aluminum in gut tissue of crayfish (Procambarus clarkii), purged in sodium chloride

    SciTech Connect

    Madigosky, S.R.; Alvarez-Hernandez, X.; Glass, J.

    1992-10-01

    Recent concern over the release of Al in the environment has prompted researchers and health officials to assess its effects on biological systems. Aluminum, despite being the most abundant metal in earth`s lithosphere, is normally complexed in soil and is therefore unavailable for biological assimilation. The recent advent of acid rain, however, has prompted Al release due to mobilization from surrounding sediments into the environment. This is of particular concern in aquatic environments because organisms in aquatic food chains can access and concentrate sublethal levels of Al in their tissues relatively quickly. The ingestion of affected organisms by humans may therefore pose a potential health risk. One such organism, is known to concentrate metals in a variety of tissues. In northern Louisiana, many people trap or fish for crayfish in lowland areas which lie adjacent to highways and secondary roadways. Water, soil, and crayfish from these areas are known to contain high levels of Al. Some tissues known to concentrate Al (muscle, hepatopancreas and intestine tissue and contents) are those which humans commonly consume. The ingestion of these tissues may therefore expose humans to elevated Al levels. Many people who eat crayfish often purge them in dilute concentrations (1-2%) of NaCl to rid them of contaminants and make them more palatable. We are aware of no literature which corroborates the claim that purging removes contaminating metals. The objectives of this study were to (1) document the amount of Al found in water, soil, and gut tissue of crayfish (P. clarkii) collected from a roadside wetland site; (2) determine the affect of NaCl purging on the release of Al in P. clarkii and (3) assess the differences in Al levels found between stomach tissue, stomach tissue contents, intestine tissue, and intestine contents in P. clarkii. 12 refs., 3 figs., 1 tab.

  3. Structural correspondence between uranyl chloride complexes in solution and their stability constants.

    PubMed

    Soderholm, L; Skanthakumar, S; Wilson, Richard E

    2011-05-19

    Pair-distribution functions (PDF)s were obtained from high-energy X-ray scattering (HEXS) data on a series of uranyl solutions as a function of chloride ion concentration. Analyses reveal that chloride forms only inner-sphere complexes with the uranyl, replacing inner-sphere waters such that the total uranyl coordination number decreases from 4.7 waters at [Cl(-)] = 0 m to 4.4 (1.7 water and 2.7 Cl(-)) at [Cl(-)] = 6.8 m. Some of the second-coordination sphere waters reorient upon uranyl inner-sphere chloride complexation in order to hydrogen bond with the bound anion. Similar data obtained on a series of solutions maintained at constant ionic strength are used to confirm structural assignments through determining stability constants for the addition of chloride to uranyl and comparison with published values. The stability constants, β(1) = 1.5(10) m(-1), β(2) = 0.8(4) m(-2), and β(3) = 0.4(1) m(-3), obtained in a series of solutions with constant ionic strength of 5.3 m, are in reasonable agreement with previously published results determined by solvent extraction. The agreement of stability constants supports our peak assignments for the PDF and thus our structural model for uranyl chloride complexes in solution. Using coordination numbers and speciation determined here as a function of chloride ion concentration, the monochloro species is found to have four coordinating waters in the uranyl equatorial plane, the dichoro species is found to be an equilibrium of three and two coordinating waters, and the trichloro species has only a single water in the equatorial plane. These values correspond to total average coordination numbers of 5, 4.3, and 4 for the mono-, di-, and trichlorouranyl complexes. From the equilibrium value of the dichloro species, it can be further estimated that ΔG = -0.5 kcal/mol for the conversion of five to four coordinate species. Overall, the HEXS data support the assertion that uranyl chloride correlations do exist and the results are

  4. Adsorption of N-alkylpyridinium chlorides from water and salt solutions on cellulose acetate ultrafiltration membranes

    SciTech Connect

    Klimenko, N.A.; Yaroshenko, N.A.; Kondratova, T.B.

    1988-09-01

    A study has been made of the adsorption of three homologues in the N-alkylpyridinium chloride series from water and salt solutions, over a wide range of concentrations, on cellulose acetate ultrafiltration membranes, Grades UAM-500 and UAM-150. When adsorption takes place from true solutions, the membrane surface is hydrophobized. In the region of micellar solutions, nonassociated molecules and micelles are adsorbed in the mesopores and supermicropores, forming a mosaic adsorption layer. The thickness of the modifying layer depends on the length of the hydrophobic radical and on the composition of the system.

  5. Electrochemical Behavior of Nano-grained Pure Copper in Dilute Alkaline Solution with Chloride Ion Trace

    NASA Astrophysics Data System (ADS)

    Fattah-Alhosseini, Arash; Imantalab, Omid; Attarzadeh, Farid Reza

    2016-10-01

    Effect of nano-grained structure on the interface behavior of pure copper in 0.01M KOH solution with chloride ion trace is investigated by various electrochemical techniques. Nano-grained structure was achieved by accumulative roll bonding (ARB) technique. Before any electrochemical measurements, microstructure was evaluated by means of optical microscopy and transmission electron microscopy (TEM). TEM observations showed that nano-grains (with an average size of below 100 nm) appeared after eight passes of ARB. Polarization curves revealed that increasing chloride ion concentration leads to a decrease in the corrosion and pitting potentials of both annealed and nano-grained pure copper samples. Electrochemical impedance spectroscopy revealed that chloride ion trace lowers passive film resistance and charge-transfer resistance in both annealed and nano-grained samples. Mott-Schottky analysis showed that the surface films formed on annealed and nano-grained samples in KOH solution with and without NaCl addition are of p-type semiconducting behavior. Moreover, this analysis showed that the acceptor density increases by increasing chloride ion concentration.

  6. Occurrence of aluminum in chloride cells of Perla marginata (Plecoptera) after exposure to low pH and elevated aluminum concentration

    SciTech Connect

    Guerold, F.; Giamberini, L.; Pihan, J.C.; Tourmann, J.L.; Kaufmann, R.

    1995-04-01

    As a consequence of acid depositions on poorly buffered catchments underlain by hard rocks, aluminum is mobilized and transported from terrestrial systems to the aquatic environment. Loss of fishes has been related to low pH and elevated aluminum concentrations in surface waters which present a low ionic content especially during acid stress such as snowmelt and heavy rainfalls. Among the causes of fish population decline in acid waters, aluminum is considered a toxic cofactor. Different studies have clearly shown that aluminum is accumulated in different organs such as kidneys, liver and gills. Research on fish has demonstrated that aluminum may be toxic, but the toxicity is markedly influenced by the pH, organic compounds and calcium content of the water. Field surveys have shown clearly that macroinvertebrates are also affected by surface-water acidification. However, little is know about the possible effects of aluminum on aquatic invertebrates and, particularly, on aquatic insects exposed to acidic conditions. Hall et al. have shown that the whole-body concentration of aluminum decreases in blackflies and mayflies transplated from neutral water to acid water. Similar results have been reported for Daphnia and chironomid. On the contrary, Ormerod et al. demonstrated the absence of relationship between water pH and insect aluminum concentrations. When aluminum occurs in aquatic insects, it has been shown that it is primarily adsorbed on the external surface and/or accumulates in gut contents. To our knowledge, the subcellular location as well as the toxicity of aluminum to acid-sensitive aquatic insects remains unclear and existing hypotheses are often based on research on fish. In this content the purpose of this study was to investigate the presence of aluminum at a subcellular level in the acid-sensitive species of stonefly, Perla marginata, after exposure to low pH and elevated aluminum concentrations. 18 refs., 1 fig., 1 tab.

  7. Desorption of CO2 from low concentration monoethanolamine solutions using calcium chloride and ultrasound irradiation

    NASA Astrophysics Data System (ADS)

    Tanaka, Kosuke; Okawa, Hirokazu; Fujiwara, Tatsuo; Kato, Takahiro; Sugawara, Katsuyasu

    2015-07-01

    We developed an effective method for desorbing CO2 from low-concentration (0.2 mol/l) monoethanolamine (MEA) solutions using calcium chloride (CaCl2) and ultrasound irradiation at 25 °C. The proportion of CO2 desorbed from the MEA solution was calculated from the amount of CaCO3 generated and the amount of CO2 emitted. The proportion of CO2 desorbed from the MEA solution was much higher when CaCl2 was added than when CaCl2 was not added. We also characterized the CaCO3 that was generated when the solution was treated with ultrasound irradiation and when the solution was stirred. The CaCO3 particles produced were more homogeneous and smaller when ultrasound irradiation was applied than when the solution was stirred.

  8. Resistance of Pseudomonas to Quaternary Ammonium Compounds. I. Growth in Benzalkonium Chloride Solution

    PubMed Central

    Adair, Frank W.; Geftic, Sam G.; Gelzer, Justus

    1969-01-01

    Resistant cells of Pseudomonas aeruginosa and a waterborne Pseudomonas sp. (strain Z-R) were able to multiply in nitrogen-free minimal salts solution containing various concentrations of commercially prepared, ammonium acetate-buffered benzalkonium chloride (CBC), a potent antimicrobial agent. As the CBC concentration increased, growth increased until a point was reached at which the extent of growth leveled off or was completely depressed. Minimal salts solutions of pure benzalkonium chloride (PBC) containing no ammonium acetate did not support bacterial growth. When ammonium acetate was added to PBC solutions in the same concentrations found in CBC solutions, growth patterns developed that were comparable to those found with CBC. Likewise, (NH4)2SO4 added to PBC solutions supported growth of both organisms. P. aeruginosa was initially resistant to CBC levels of 0.02% and it was adapted to tolerate levels as high as 0.36%. Strain Z-R was naturally resistant to 0.4% CBC. Since ammonium acetate, carried over by the CBC used in drug formulations and disinfectant solutions, has the potential to support the growth of resistant bacteria and thus make possible the risk of serious infection, it is suggested that regulations allowing the presence of ammonium acetate in CBC solution be reconsidered. PMID:4984761

  9. Crystallization of sodium chloride from a concentrated calcium chloride-potassium chloride-sodium chloride solution in a CMSMPR crystallizer: Observation of crystal size distribution and model validation

    NASA Astrophysics Data System (ADS)

    Choi, Byung Sang

    Compared to overwhelming technical data available in other advanced technologies, knowledge about particle technology, especially in particle synthesis from a solution, is still poor due to the lack of available equipment to study crystallization phenomena in a crystallizer. Recent technical advances in particle size measurement such as Coulter counter and laser light scattering have made in/ex situ study of some of particle synthesis, i.e., growth, attrition, and aggregation, possible with simple systems. Even with these advancements in measurement technology, to grasp fully the crystallization phenomena requires further theoretical and technical advances in understanding such particle synthesis mechanisms. Therefore, it is the motive of this work to establish the general processing parameters and to produce rigorous experimental data with reliable performance and characterization that rigorously account for the crystallization phenomena of nucleation, growth, aggregation, and breakage including their variations with time and space in a controlled continuous mixed-suspension mixed-product removal (CMSMPR) crystallizer. This dissertation reports the results and achievements in the following areas: (1) experimental programs to support the development and validation of the phenomenological models and generation of laboratory data for the purpose of testing, refining, and validating the crystallization process, (2) development of laboratory well-mixed crystallizer system and experimental protocols to generate crystal size distribution (CSD) data, (3) the effects of feed solution concentration, crystallization temperature, feed flow rate, and mixing speed, as well as different types of mixers resulting in the evolution of CSDs with time from a concentrated brine solution, (4) with statistically designed experiments the effects of processing variables on the resultant particle structure and CSD at steady state were quantified and related to each of those operating

  10. Coenzyme Q10 and fish oil synergistically alleviate aluminum chloride-induced suppression of testicular steroidogenesis and antioxidant defense.

    PubMed

    Mohammad, Nanies Sameeh; Arafa, Manar Hamed; Atteia, Hebatallah Husseini

    2015-01-01

    Aluminum (Al) is an environmental xenobiotic that stimulates free radical generation and hence reproductive toxicity. Coenzyme Q10 (CoQ10) effectively counteracts free radical-induced tissue damage. Omega-3 polyunsaturated fatty acids present in fish oil (FO) exert beneficial effects on reproduction in male animals. This study therefore investigated the effects of both agents on testicular dysfunction induced by aluminum chloride (AlCl3). Fifty male rats were gavaged with either 1% gum acacia (control group) or AlCl3 (34 mg/kg/day) for ten weeks. Concurrently, AlCl3-treated rats received no treatment, CoQ10 (10 mg/kg/day, p.o.), and/or FO (400 mg/kg/day, p.o.) for ten weeks. AlCl3 caused a significant decrease in serum testosterone, luteinizing hormone (LH), and follicular stimulating hormone (FSH), as well as testicular weight, antioxidant enzyme gene expression and activities, reduced glutathione, zinc, adenosine 3',5'-cyclic monophosphate (cAMP) contents, and number of Leydig cells, along with down-regulation of 3beta-hydroxysteroid dehydrogenase (3β-HSD), 17β-HSD, steroidogenic acute regulatory protein (STAR), and cholesterol side-chain cleavage enzyme (P450scc) gene expression. However, testicular Al, malondialdehyde (MDA), and nitric oxide (NO) levels were markedly increased. Treatment with CoQ10 and FO, alone or in combined form led to an improvement in the aforementioned biomarkers. Overall, individual or combined treatment with CoQ10 and FO could ameliorate the toxic effects of AlCl3 on testicular tissues by mechanisms related to their potent antioxidant potential and stimulatory effects on steroidogenic enzymes transcription. CoQ10 seems to be better than FO regarding oxidative and nitrosative stress, Zn deficiency, and Al overload. However, FO showed more pronounced effect than CoQ10 on hormones, steroidogenic markers, and cAMP. A cocktail of both demonstrated greater protective effects on testicular tissues than monotherapy.

  11. Performance of cellulose acetate butyrate membranes in hyperfiltration of sodium chloride and urea feed solution

    NASA Technical Reports Server (NTRS)

    Wydeven, T.; Leban, M.

    1973-01-01

    Cellulose acetate butyrate (CAB) membranes are shown to give high salt and urea rejection with water flux of about 3 gallons/sq ft per day at 600 psig. Membranes prepared from a formulation containing glyoxal show a significant increase in flux and decrease in salt and urea rejection with drying time. Zero drying time gives maximum urea and salt rejection and is therefore most suitable for hyperfiltration of sodium chloride and urea feed solution.

  12. Interdiffusion in Ternary Magnesium Solid Solutions of Aluminum and Zinc

    DOE PAGES

    Kammerer, Catherine; Kulkarni, Nagraj S; Warmack, Robert J Bruce; ...

    2016-01-11

    Al and Zn are two of the most common alloying elements in commercial Mg alloys, which can improve the physical properties through solid solution strengthening and precipitation hardening. Diffusion plays a key role in the kinetics of these and other microstructural design relevant to Mg-alloy development. However, there is a lack of multicomponent diffusion data available for Mg alloys. Through solid-to-solid diffusion couples, diffusional interactions of Al and Zn in ternary Mg solid-solution at 400° and 450 °C were examined by an extension of the Boltzmann-Matano analysis based on Onsager s formalism. Concentration profiles of Mg-Al-Zn ternary alloys were determinedmore » by electron probe microanalysis, and analyzed to determine the ternary interdiffusion coefficients as a function of composition. Zn was determined to interdiffuse the fastest, followed by Mg and Al. Appreciable diffusional interactions among Mg, Al, and Zn were observed by variations in sign and magnitude of cross interdiffusion coefficients. In particular, Zn was found to significantly influence the interdiffusion of Mg and Al significantly: the and ternary cross interdiffusion coefficients were both negative, and large in magnitude, in comparison to and , respectively. Al and Mg were observed influence the interdiffusion of Mg and Al, respectively, with positive and interdiffusion coefficients, but their influence on the Zn interdiffusion was negligible.« less

  13. Interdiffusion in Ternary Magnesium Solid Solutions of Aluminum and Zinc

    SciTech Connect

    Kammerer, Catherine; Kulkarni, Nagraj S; Warmack, Robert J Bruce; Sohn, Yong Ho

    2016-01-11

    Al and Zn are two of the most common alloying elements in commercial Mg alloys, which can improve the physical properties through solid solution strengthening and precipitation hardening. Diffusion plays a key role in the kinetics of these and other microstructural design relevant to Mg-alloy development. However, there is a lack of multicomponent diffusion data available for Mg alloys. Through solid-to-solid diffusion couples, diffusional interactions of Al and Zn in ternary Mg solid-solution at 400° and 450 °C were examined by an extension of the Boltzmann-Matano analysis based on Onsager s formalism. Concentration profiles of Mg-Al-Zn ternary alloys were determined by electron probe microanalysis, and analyzed to determine the ternary interdiffusion coefficients as a function of composition. Zn was determined to interdiffuse the fastest, followed by Mg and Al. Appreciable diffusional interactions among Mg, Al, and Zn were observed by variations in sign and magnitude of cross interdiffusion coefficients. In particular, Zn was found to significantly influence the interdiffusion of Mg and Al significantly: the and ternary cross interdiffusion coefficients were both negative, and large in magnitude, in comparison to and , respectively. Al and Mg were observed influence the interdiffusion of Mg and Al, respectively, with positive and interdiffusion coefficients, but their influence on the Zn interdiffusion was negligible.

  14. Synthesis and Characterization of ZnO Nanorods and Nanodisks from Zinc Chloride Aqueous Solution.

    PubMed

    Long, Tengfa; Yin, Shu; Takabatake, Kouta; Zhnag, Peilin; Sato, Tsugio

    2008-12-16

    ZnO nanorods and nanodisks were synthesized by solution process using zinc chloride as starting material. The morphology of ZnO crystal changed greatly depending on the concentrations of Zn(2+) ion and ethylene glycohol (EG) additive in the solution. The effect of thermal treatment on the morphology was investigated. Photocatalytic activities of plate-like Zn(5)(OH)(8)Cl(2) . H(2)O and rod-like ZnO were characterized. About 18% of 1 ppm NO could be continuously removed by ZnO particles under UV light irradiation.

  15. Synthesis and Characterization of ZnO Nanorods and Nanodisks from Zinc Chloride Aqueous Solution

    PubMed Central

    2009-01-01

    ZnO nanorods and nanodisks were synthesized by solution process using zinc chloride as starting material. The morphology of ZnO crystal changed greatly depending on the concentrations of Zn2+ion and ethylene glycohol (EG) additive in the solution. The effect of thermal treatment on the morphology was investigated. Photocatalytic activities of plate-like Zn5(OH)8Cl2 · H2O and rod-like ZnO were characterized. About 18% of 1 ppm NO could be continuously removed by ZnO particles under UV light irradiation. PMID:20596478

  16. Corrosion Behavior of Alloy 22 in Oxalic Acid and Sodium Chloride Solutions

    SciTech Connect

    Day, S D; Whalen, M T; King, K J; Hust, G A; Wong, L L; Estill, J C; Rebak, R B

    2003-06-24

    Nickel based Alloy 22 (NO6022) is extensively used in aggressive industrial applications, especially due to its resistance to localized corrosion and stress corrosion cracking in high chloride environments. The purpose of this work was to characterize the anodic behavior of Alloy 22 in oxalic acid solution and to compare its behavior to sodium chloride (NaCl) solutions. Standard electrochemical tests such as polarization resistance and cyclic polarization were used. Results show that the corrosion rate of Alloy 22 in oxalic acid solutions increased rapidly as the temperature and the acid concentration increased. Extrapolation studies show that even at a concentration of 10{sup -4}M oxalic acid, the corrosion rate of Alloy 22 would be higher in oxalic acid than in 1 M NaCl solution. Alloy 22 was not susceptible to localized corrosion in oxalic acid solutions. Cyclic polarization tests in 1 M NaCl showed that Alloy 22 was susceptible to crevice corrosion at 90 C but was not susceptible at 60 C.

  17. Adsorption and chemical reaction of gaseous mixtures of hydrogen chloride and water on aluminum oxide and application to solid-propellant rocket exhaust clouds

    NASA Technical Reports Server (NTRS)

    Cofer, W. R., III; Pellett, G. L.

    1978-01-01

    Hydrogen chloride (HCl) and aluminum oxide (Al2O3) are major exhaust products of solid rocket motors (SRM). Samples of calcination-produced alumina were exposed to continuously flowing mixtures of gaseous HCl/H2O in nitrogen. Transient sorption rates, as well as maximum sorptive capacities, were found to be largely controlled by specific surface area for samples of alpha, theta, and gamma alumina. Sorption rates for small samples were characterized linearly with an empirical relationship that accounted for specific area and logarithmic time. Chemisorption occurred on all aluminas studied and appeared to form from the sorption of about a 2/5 HCl-to-H2O mole ratio. The chemisorbed phase was predominantly water soluble, yielding chloride/aluminum III ion mole ratios of about 3.3/1 suggestive of dissolved surface chlorides and/or oxychlorides. Isopiestic experiments in hydrochloric acid indicated that dissolution of alumina led to an increase in water-vapor pressure. Dissolution in aqueous SRM acid aerosol droplets, therefore, might be expected to promote evaporation.

  18. Removal of sodium and chloride ions from aqueous solutions using fique fibers (Furcraea spp.).

    PubMed

    Agudelo, Nikolay; Hinestroza, Juan P; Husserl, Johana

    2016-01-01

    Fique fibers obtained from the leaves of Furcraea spp., a highly abundant plant in the mountains of South America, may offer an alternative as biosorbents in desalination processes as they exhibit high removal capacities (13.26 meq/g for chloride ions and 15.52 meq/g for sodium ions) up to four times higher than exchange capacities commonly observed in synthetic resins. The ion removal capacity of the fibers was also found to be a function of the pH of the solution with the maximum removal of ions obtained at pH 8. Unlike most commercial ion exchange resins, our results suggest that fique fibers allow simultaneous removal of chloride and sodium ions.

  19. Superiority of experts over novices in trueness and precision of concentration estimation of sodium chloride solutions.

    PubMed

    Masuda, Tomohiro; Wada, Yuji; Okamoto, Masako; Kyutoku, Yasushi; Yamaguchi, Yui; Kimura, Atsushi; Kobayakawa, Tatsu; Kawai, Takayuki; Dan, Ippeita; Hayakawa, Fumiyo

    2013-03-01

    Several studies have reported that experts outperform novices in specific domains. However, the superiority of experts in accuracy, taking both trueness and precision into consideration, has not yet been explored. Here, we examined differences between expert and novice performances by evaluating the accuracy of their estimations of physical concentrations of sodium chloride in solutions while employing a visual analog scale. In Experiment 1, 14 experts and 13 novices tasted 6 concentrations of the solutions until they had learned their intensities. Subsequently, they repeatedly rated the concentration of 3 other solutions in random order. Although we did not find a difference between the performances of the 2 groups in trueness (difference between rating and correct concentration), the precision (consistency of ratings for each participant) of experts was higher than that of novices. In Experiment 2, 13 experts who had participated in Experiment 1 and 10 experts and 12 novices who had not participated in Experiment 1 rated the salt concentration in sodium chloride/sucrose mixtures in the same way as in Experiment 1. Both trueness and precision of performance were higher in both expert groups than in the novice group. By introducing precision and trueness parameters, we succeeded in quantifying the estimations of experts and novices in rating the concentration of solutions, revealing experts' superiority even for a task they had not been trained for.

  20. Study of plasma coagulation induced by contact with calcium chloride solution.

    PubMed

    Shida, Natsumi; Kurasawa, Ryuta; Maki, Yasuyuki; Toyama, Yoshiharu; Dobashi, Toshiaki; Yamamoto, Takao

    2016-11-28

    Blood coagulation capability is one of the most important factors for the diagnosis of patients with thrombosis. Regarding the blood coagulation as an example of gelation of soft matter, we can apply an analytical method to this phenomenon and pick up some relevant parameters. In various systems, gelation dynamics induced by contact between a polymer solution and a crosslinker solution are well explained by the "moving boundary picture" (Yamamoto et al., J. Phys. Chem. B, 2010, 114, 10002-10009). The aim of this paper is to clarify whether this picture can be applied to a clinically important biological system used for blood coagulation tests. We have measured the time course of the thickness of a plasma gel layer formed when plasma comes in contact with calcium chloride solution in a rectangular cell and analyzed theoretically on the basis of the moving boundary picture. The entire process was well expressed using a scaled equation involving three parameters characterizing the plasma, k, Kin, and β, where k is the time required to reach the incipient stage of three-dimensional network formation, the parameter Kin is proportional to calcium chloride concentration and β is a constant. These results indicate the direct applicability of the general theory of gelation dynamics induced by contact between two solutions to the in vitro coagulation (gelation) of plasma, and the fitting parameters may be used for diagnosis.

  1. Porous aluminum room temperature anodizing process in a fluorinated-oxalic acid solution

    NASA Astrophysics Data System (ADS)

    Dhahri, S.; Fazio, E.; Barreca, F.; Neri, F.; Ezzaouia, H.

    2016-08-01

    Anodizing of aluminum is used for producing porous insulating films suitable for different applications in electronics and microelectronics. Porous-type aluminum films are most simply realized by galvanostatic anodizing in aqueous acidic solutions. The improvement in application of anodizing technique is associated with a substantial reduction of the anodizing voltage at appropriate current densities as well as to the possibility to carry out the synthesis process at room temperature in order to obtain a self-planarizing dielectric material incorporated in array of super-narrow metal lines. In this work, the anodizing of aluminum to obtain porous oxide was carried out, at room temperature, on three different substrates (glass, stainless steel and aluminum), using an oxalic acid-based electrolyte with the addition of a relatively low amount of 0.4 % of HF. Different surface morphologies, from nearly spherical to larger porous nanostructures with smooth edges, were observed by means of scanning electron microscopy. These evidences are explained by considering the formation, transport and adsorption of the fluorine species which react with the Al3+ ions. The behavior is also influenced by the nature of the original substrate.

  2. Stability of the grain structure in 2219-O aluminum alloy friction stir welds during solution treatment

    SciTech Connect

    Chen, Y.C. . E-mail: armstrong@hit.edu.cn; Feng, J.C.; Liu, H.J.

    2007-02-15

    The stability of the grain structure in 2219-O aluminum alloy friction stir welds during solution treatment has been investigated. Experimental results show that the solution treatment causes drastic grain growth, Grain growth initiates at the surface and the bottom of the weld and then extends to the weld centre within several minutes. The solution treatment temperature and the welding heat input have a significant effect on grain growth. The higher the solution temperature, or the higher the welding heat input, the greater the grain growth. The instability of the grains is attributed to an imbalance between thermodynamic driving forces for grain growth and the pinning forces impeding grain boundary migration during solution treatment.

  3. Production of aluminum metal by electrolysis of aluminum sulfide

    DOEpatents

    Minh, N.Q.; Loutfy, R.O.; Yao, N.P.

    1982-04-01

    Metallic aluminum may be produced by the electrolysis of Al/sub 2/S/sub 3/ at 700 to 800/sup 0/C in a chloride melt composed of one or more alkali metal chlorides, and one or more alkaline earth metal chlorides and/or aluminum chloride to provide improved operating characteristics of the process.

  4. Production of aluminum metal by electrolysis of aluminum sulfide

    DOEpatents

    Minh, Nguyen Q.; Loutfy, Raouf O.; Yao, Neng-Ping

    1984-01-01

    Production of metallic aluminum by the electrolysis of Al.sub.2 S.sub.3 at 700.degree.-800.degree. C. in a chloride melt composed of one or more alkali metal chlorides, and one or more alkaline earth metal chlorides and/or aluminum chloride to provide improved operating characteristics of the process.

  5. Testing Room-Temperature Ionic Liquid Solutions for Depot Repair of Aluminum Coatings

    DTIC Science & Technology

    2011-05-01

    Liquid : Definition Table Salt (NaCl) Crystal Melting Point = 801 C Ionic Liquid (BMIM-PF6) Melting Point = 11 C An “ionic liquid ” (IL) is a salt in...Testing Room-Temperature Ionic Liquid Solutions for Depot Repair of Aluminum Coatings Elizabeth Berman, Ph.D., AFRL/RXSCP Natasha Voevodin, Ph.D...TYPE 3. DATES COVERED 00-00-2011 to 00-00-2011 4. TITLE AND SUBTITLE Testing Room-Temperature Ionic Liquid Solutions for Depot Repair of

  6. PROCESS OF ELECTROPLATING METALS WITH ALUMINUM

    DOEpatents

    Schickner, W.C.

    1960-04-26

    A process of electroplating aluminum on metals from a nonaqueous bath and a novel method of pretreating or conditioning the metal prior to electrodeposition of the aluminum are given. The process of this invention, as applied by way of example to the plating of uranium, comprises the steps of plating the uranium with the barrier inetal, immersing the barrier-coated uranium in fatty acid, and electrolyzing a water-free diethyl ether solution of aluminum chloride and lithium hydride while making the uranium the cathode until an aluminum deposit of the desired thickness has been formed. According to another preferred embodiment the barrier-coated uranium is immersed in an isopropyl alcohol solution of sterato chromic chloride prior to the fatty acid treatment of this invention.

  7. Compatibility and stability of potassium chloride and magnesium sulfate in 0.9% sodium chloride injection and 5% dextrose injeciton solutions.

    PubMed

    Quay, I; Tan, E

    2001-01-01

    The compatibility and stability of 80 mmol/L potassium chloride and 16 mmol/L magnesium sulfate in 0.9% sodium chloride injection and in 5% dextrose injection solutions at 22 deg C have been studied by means of a Beckman Clinical Chemistry Analyzer Synchron CX5 Delta. The infusions were stable for 24 hours at 22 deg C. The results from both diluents showed an average of +/-5% fluctuations in concentration. None of the samples appeared to form visible precipitation or to change in color or clarity.

  8. Comparative estimate of the efficiency of the sorption extraction of iodine from chloride solutions

    NASA Astrophysics Data System (ADS)

    Nguen, Bao Din Kuok; Chernov'yants, M. S.; Burykin, I. V.; Anokhin, A. S.

    2012-12-01

    The possibility of applying activated carbon and polymeric sorbents poly(4-vinylpyridine), polytrimethylsilylpropyne (PTMSP), bromo-substituted PNMSP (Br-PNMSP), poly(N-methyl-4-vinylpyridinium iodide) for the sorption recovery of iodine from a 0.5 M solution of sodium chloride is studied. The dependence of iodine sorption on the pH of solution, the amount of adsorbent, and the duration of contact between the solution and adsorbent is studied. The highest sorption capacity ( G = 616.78 mg/g) is attained by using poly(N-methyl-4-vinylpyridinium iodide) anionite with the addition of iodine to form complex triiodide ions. The dynamics of iodine adsorption on poly(4-vinylpyridine) is described by a kinetic model of pseudosecond order. The composition and structure of the iodine compounds sorbed by polymers and activated carbon are studied by Raman spectroscopy (RS).

  9. Kinetics of sorption of niobium ions by anion-exchangers from mixed chloride-fluoride solutions

    SciTech Connect

    Rychkov, V.N.; Pakholkov, V.S.; Kuznetsova, L.D.

    1987-08-10

    The authors showed earlier on the basis of experimental and calculated data obtained in studies of ion-exchange equilibrium that the sorbability and composition of sorbed niobium ions are determined by the content of hydrofluoric acid in mixed chloride-fluoride solutions. Variation of the ionic state of niobium in these solutions should also influence the rate of ion exchange. In this communication they examine the results of a study of the kinetics of exchange of niobium ions on AV-17 x 8, EDE-10P, and AN-2F anion-exchange resins in fluoride-containing solutions. Kinetic curves for sorption of niobium ions and the results of their evaluation are presented.

  10. Solute Enhanced Strain Hardening of Aluminum Alloys to Achieve Improved Combinations of Strength and Toughness

    NASA Astrophysics Data System (ADS)

    Hovanec, Christopher James

    2011-12-01

    The feasibility of achieving improved combinations of strength and toughness in aluminum alloy 2524 through solute enhanced strain hardening (SESH) has been explored in this study and shown to be viable. The effectiveness of SESH is directly dependent on the strain hardening rate (SHR) of the material being processed. Aluminum alloy 2524 naturally ages to the T4-temper after solution heat treating and quenching. The SHR of strain free and post cold rolled material as a function of natural aging time has been measured by means of simple compression. It has been determined that the SHR of AA2524 is more effective with solute in solution rather than clustered into GP zones. It has also been shown that the typical rapid formation of GP zones at room temperature (natural aging) is inhibited by moderate cold rolling strains (□CR ≥ 0.2) through dislocation aided vacancy annihilation. The practical limitations of quenching rate have been determined using hardness and eddy current electrical conductivity measurements. It has been shown that too slow of a quench rate results in solute being lost to both the formation of GP zones and embrittling precipitates during the quench, while too rapid of a quench rate results in mid-plane cracking of the work piece during the SESH processing. The mid-plane cracking was overcome by using an uphill quenching procedure to relieve residual stresses within the work piece. Aluminum alloy 2524 strengthened through SESH to a yield strength 11% greater than that in the T6-Temper exhibits: equivalent toughness, 5% greater UTS, 1% greater elongation, 7% greater R.A., and absorbs 15% more energy during tensile testing. At yield strengths comparable to published data for 2x24 alloys, the SESH 2524 exhibited up to a 60% increase in fracture toughness. The fractured surfaces of the SESH material exhibited transgranular dimpled rupture as opposed to the grain boundary ductile fracture (GBPF) observed in the artificially aged material.

  11. Comparison of Sodium Chloride Tablets-Induced, Sodium Chloride Solution-Induced, and Glycerol-Induced Hyperhydration on Fluid Balance Responses in Healthy Men.

    PubMed

    Savoie, Félix A; Asselin, Audrey; Goulet, Eric D B

    2016-10-01

    Savoie, FA, Asselin, A, and Goulet, EDB. Comparison of sodium chloride tablets-induced, sodium chloride solution-induced, and glycerol-induced hyperhydration on fluid balance responses in healthy men. J Strength Cond Res 30(10): 2880-2891, 2016-Sodium chloride solution-induced hyperhydration (NaCl-SolIH) is a powerful strategy to increase body water before exercise. However, NaCl-SolIH is associated with an unpleasant salty taste, potentially dissuading some athletes from using it and coaches from recommending it. Therefore, we evaluated the hyperhydrating potential of sodium chloride tablets-induced hyperhydration (NaCl-TabIH), which bypasses the palatability issue of NaCl-SolIH without sacrificing sodium chloride content, and compared it to NaCl-SolIH and glycerol-induced hyperhydration (GIH). Sixteen healthy males (age: 21 ± 2 years; fat-free mass (FFM): 65 ± 6 kg) underwent three, 3-hour long passive hyperhydration protocols during which they drank, over the first 60 minutes, 30-ml·kg FFM of an artificially sweetened solution. During NaCl-TabIH, participants swallowed 7.5, 1 g each, sodium chloride tablets with every liter of solution. During NaCl-SolIH, an equal quantity of sodium chloride tablets was dissolved in each liter of solution. With GIH, the glycerol concentration was 46.7 g·L. Urine production, fluid retention, hemoglobin, hematocrit, plasma volume, and perceptual variables were monitored throughout the trials. Total fluid intake was 1948 ± 182 ml. After 3 hour, there were no significant differences among treatments for hemoglobin, hematocrit, and plasma volume changes. Fluid retention was significantly greater with NaCl-SolIH (1150 ± 287 ml) than NaCl-TabIH (905 ± 340 ml) or GIH (800 ± 211 ml), with no difference between NaCl-TabIH and GIH. No differences were found among treatments for perceptual variables. NaCl-TabIH and GIH are equally effective, but inferior than NaCl-SolIH. NaCl-TabIH represents an alternative to hyperhydration induced

  12. [Aluminum dissolution and changes of pH in soil solution during sorption of copper by aggregates of paddy soil].

    PubMed

    Xu, Hai-Bo; Zhao, Dao-Yuan; Qin, Chao; Li, Yu-Jiao; Dong, Chang-Xun

    2014-01-01

    Size fractions of soil aggregates in Lake Tai region were collected by the low-energy ultrasonic dispersion and the freeze-desiccation methods. The dissolution of aluminum and changes of pH in soil solution during sorption of Cu2+ and changes of the dissolution of aluminum at different pH in the solution of Cu2+ by aggregates were studied by the equilibrium sorption method. The results showed that in the process of Cu2+ sorption by aggregates, the aluminum was dissoluted and the pH decreased. The elution amount of aluminum and the decrease of pH changed with the sorption of Cu2+, both increasing with the increase of Cu2+ sorption. Under the same conditions, the dissolution of aluminum and the decrease of pH were in the order of coarse silt fraction > silt fraction > sand fraction > clay fraction, which was negatively correlated with the amount of iron oxide, aluminum and organic matter. It suggested that iron oxide, aluminum and organic matters had inhibitory and buffering effect on the aluminum dissolution and the decrease of pH during the sorption of Cu2+.

  13. Photodynamic therapy of murine non-melanoma skin carcinomas with diode laser after topical application of aluminum phthalocyanine chloride

    NASA Astrophysics Data System (ADS)

    Kyriazi, Maria; Alexandratou, Eleni; Yova, Dido; Rallis, Michail; Trebst, Tilmann

    2007-07-01

    The aim of this work is to study pharmacokinetics and photodynamic efficiency of aluminium phthalocyanine chloride (AlClPc) in dimethylsulfoxide/Tween 80/water solution, after topical application on hairless mice bearing non-melanoma skin carcinomas. The concentration of photosensitizer in normal skin and tumor biopsies 1-6 hours after application was assessed by fluorescence spectroscopy of chemical extractions. The concentration of photosensitizer was 40 times higher in tumor than in normal skin even 1 h after application. For photodynamic therapy (PDT) AlClPc was excited by a diode laser emitting at 670 nm, 1 h after application. Seven different combinations of therapeutic parameters were chosen. The efficiency was assessed as the percentage of complete tumor remission, the tumor growth retardation and the cosmetic outcomes. The highest complete remission 60% was achieved with the combination of 75 mW/cm2 with 150 J/cm2. No recurrence rate was observed in any treatment parameters group and the cosmetic outcome in all completely treated tumors was excellent. The results show that the effectiveness of PDT is highly dependent on fluence rate. In addition, they are promising for further investigation of this PDT scheme in preclinical studies mainly in non-melanoma skin carcinomas up to 7mm.

  14. Impact of aluminum chloride on process performance and microbial community structure of granular sludge in an upflow anaerobic sludge blanket reactor for natural rubber processing wastewater treatment.

    PubMed

    Thanh, Nguyen Thi; Watari, Takahiro; Thao, Tran Phuong; Hatamoto, Masashi; Tanikawa, Daisuke; Syutsubo, Kazuaki; Fukuda, Masao; Tan, Nguyen Minh; Anh, To Kim; Yamaguchi, Takashi; Huong, Nguyen Lan

    In this study, granular sludge formation was carried out using an aluminum chloride supplement in an upflow anaerobic sludge blanket (UASB) reactor treating natural rubber processing wastewater. Results show that during the first 75 days after the start-up of the UASB reactor with an organic loading rate (OLR) of 2.65 kg-COD·m(-3)·day(-1), it performed stably with a removal of 90% of the total chemical oxygen demand (COD) and sludge still remained in small dispersed flocs. However, after aluminum chloride was added at a concentration of 300 mg·L(-1) and the OLR range was increased up to 5.32 kg-COD·m(-3)·day(-1), the total COD removal efficiency rose to 96.5 ± 2.6%, with a methane recovery rate of 84.9 ± 13.4%, and the flocs began to form granules. Massively parallel 16S rRNA gene sequencing of the sludge retained in the UASB reactor showed that total sequence reads of Methanosaeta sp. and Methanosarcina sp., reported to be the key organisms for granulation, increased after 311 days of operation. This indicates that the microbial community structure of the retained sludge in the UASB reactor at the end of the experiment gave a good account of itself in not only COD removal, but also granule formation.

  15. Experimental study on the stress corrosion cracking behavior of AISI347 in acid chloride ion solution

    NASA Astrophysics Data System (ADS)

    Qu, Yanpeng; Wang, Runkun; Wang, Chao; Chen, Songying

    The stress corrosion cracking (SCC) behavior of AISI347 austenitic stainless steel exposed to acid solution containing chloride ion at different temperature and pressure is studied through slow strain rate testing (SSRT) at different test condition. The result of SSRT shows, with the pressure increasing, the SCC resistance is getting worse and the trend of brittle fracture presented by the fracture surface is more obvious. With the temperature rising, the mechanical properties of AISI347 getting worse first and then getting better, it gets to be the worst when the temperature is 260 °C. The result of significance effect analysis of temperature and pressure on SCC shows that the temperature has a greater effect on the resistance to SCC of AISI347 austenitic stainless steel than the pressure. The main component of passive film is analyzed and the mechanism of SCC is discussed. Chromium oxides soluble in the acidic chloride solution results in the forming of corrosion pits and the cracking of the passive film under stress.

  16. Simultaneous leaching of Pt, Pd and Rh from automotive catalytic converters in chloride-containing solutions

    NASA Astrophysics Data System (ADS)

    Hasani, M.; Khodadadi, A.; Koleini, S. M. J.; Saeedi, A. H.; Meléndez, A. M.

    2017-01-01

    Dissolution of platinum group metals (PGM; herein Pt, Pd and Rh) in different chloride-based leaching systems from spent auto catalysts was performed. Response surface methodology and a five-level-five-factor central composite design were used to evaluate the effects of 1) temperature, 2) liquid-to-solid ratio, 3) stirring speed, 4) acid concentration and 5) particle size on extraction yield of PGM by aqua regia. Analysis of variance was used to determine the optimum conditions and most significant factors affecting the overall metal extraction. In the optimum conditions, leaching of Pt, Pd and Rh was 91.58%, 93.49% and 60.15%, respectively. The effect of different oxidizing agents on the PGM dissolution in chloride medium was studied comparatively in the following leaching systems: a) aqua regia/sulfuric acid mixture, b) hydrogen peroxide in sulfuric acid (piranha solution), c) sodium hypochlorite and d) copper(II). Dissolution of Rh is increased in both aqua regia and hydrogen peroxide/hydrochloric acid solutions by adding sulfuric acid.

  17. Light-induced genetic toxicity of thimerosal and benzalkonium chloride in commercial contact lens solutions.

    PubMed

    Lovely, T J; Levin, D E; Klekowski, E

    1982-03-01

    Several commercial solutions used for daily care of contact lenses were tested for mutagenicity in 4 strains of Salmonella and for their ability to induce repairable DNA damage in the E. coli DNA polymerase A- assay. 5 of the 13 solutions tested were positive in the polymerase A- assay. These products demonstrated an increased level of genetic toxicity when the assay was conducted under conditions of illumination with visible light. Investigation of the genetic toxicity of some of their components, specifically the preservatives, indicated that thimerosal and benzalkonium chloride were capable of causing repairable DNA damage. Thimerosal was active only when the plates were incubated under conditions of illumination, and thus was light-induced. Benzalkonium chloride was active under conditions of dark incubation, and its genetic toxicity was enhanced when the plates were irradiated with visible light. These results were confirmed in a parallel experiment, in which cells were treated with the test agent and irradiated for a short period in liquid culture and viable cells then determined. None of the commercial products and none of the components tested, were mutagenic in the Salmonella assay.

  18. Equilibrium dialysis and ultrafiltration investigations of perchlorate removal from aqueous solution using poly(diallyldimethylammonium) chloride.

    PubMed

    Roach, Jim D; Tush, Daniel

    2008-02-01

    Use of perchlorate salts in military activities and the aerospace industry is widespread. These salts are highly water-soluble and are, to a large extent, kinetically inert as aqueous species. As a groundwater contaminant, perchlorate is now being detected in an increasing number of locations and is believed to interfere with the uptake of iodide by the thyroid, which can result in decreased hormone production. The United States Environmental Protection Agency (US EPA) has established a reference dose for perchlorate of 0.0007 mg/kg/day, which translates to a drinking water equivalent level of 24.5 ppb. This study investigated the application of polyelectrolyte-enhanced ultrafiltration (PEUF) for the selective removal of perchlorate from aqueous solution through equilibrium dialysis and ultrafiltration experiments. Using poly(diallyldimethylammonium) chloride, the effectiveness and efficiency of PEUF in the removal of perchlorate from other aqueous solution components was investigated by testing parameters such as polyelectrolyte concentration, pH, and ionic strength. Removal of perchlorate from synthetic groundwater initially containing 10.3 ppm perchlorate and also containing chloride, sulfate, and carbonate was also examined. Perchlorate separations of greater than 95% were achieved, even in the presence of 10-fold excesses of competing ions.

  19. Mid-infrared spectroscopic analysis of saccharides in aqueous solutions with sodium chloride.

    PubMed

    Kanou, Mikihito; Kameoka, Takaharu; Suehara, Ken-Ichiro; Hashimoto, Atsushi

    2017-04-01

    The infrared spectral characteristics of three different types of disaccharides (trehalose, maltose, and sucrose) and four different types of monosaccharides (glucose, mannose, galactose, and fructose) in aqueous solutions with sodium chloride (NaCl) were determined. The infrared spectra were obtained using the FT-IR/ATR method and the absorption intensities respected the interaction between the saccharide and water with NaCl were determined. This study also focused on not only the glycosidic linkage position and the constituent monosaccharides, but also the concentration of the saccharides and NaCl and found that they have a significant influence on the infrared spectroscopic characterization of the disaccharides in an aqueous solution with NaCl. The absorption intensities representing the interaction between a saccharide and water with NaCl were spectroscopically determined. Additionally, the applications of MIR spectroscopy to obtain information about saccharide-NaCl interactions in foods and biosystems were suggested.

  20. Refractive index and equation of state of a shock-compressed aqueous solution of zinc chloride

    NASA Astrophysics Data System (ADS)

    Wise, J. L.

    1983-06-01

    Velocity interferometers measurements have yielded refractive index and Hugoniot equation-of-state data for a 9.1-molar aqueous solution of zinc chloride which was shock-compressed to initial stresses ranging from 2.2 to 24.1 GPa in a series of plate-impact experiments. The Hugoniot data are accurately described by a linear variation of shock velocity with particle velocity. The optical data verify sustained solution transparency over the investigated range of shock stresses, and provide a calibration of the correction which must be applied to interferometer measurements to account for the stress-induced change in refractive index of the material. Refractive index data derived from the measured particle velocity corrections exhibit a departure from predictions based on the Gladstone-Dale relation.

  1. Effect of Sulfide Concentration on Copper Corrosion in Anoxic Chloride-Containing Solutions

    NASA Astrophysics Data System (ADS)

    Kong, Decheng; Dong, Chaofang; Xu, Aoni; Man, Cheng; He, Chang; Li, Xiaogang

    2017-02-01

    The structure and property of passive film on copper are strongly dependent on the sulfide concentration; based on this, a series of electrochemical methods were applied to investigate the effect of sulfide concentration on copper corrosion in anaerobic chloride-containing solutions. The cyclic voltammetry and x-ray photoelectron spectroscopy analysis demonstrated that the corrosion products formed on copper in anaerobic sulfide solutions comprise Cu2S and CuS. And the corrosion resistance of copper decreased with increasing sulfide concentration and faster sulfide addition, owing to the various structures of the passive films observed by the atomic force microscope and scanning electron microscope. A p-type semiconductor character was obtained under all experimental conditions, and the defect concentration, which had a magnitude of 1022-1023 cm-3, increased with increasing sulfide concentration, resulting in a higher rate of both film growth and dissolution.

  2. Corrosion of Type 7075-T73 Aluminum in a 10% HNO3 + Fe2(SO4)3 Deoxidizer Solution

    NASA Astrophysics Data System (ADS)

    Savas, Terence P.; Earthman, James C.

    2009-03-01

    Localized corrosion damage in Type 7075-T73 aluminum was investigated for a HNO3 + Fe2(SO4)3 deoxidizer solution which is frequently used for surface pretreatment prior to anodizing. The corrosion damage was quantified in the time domain using the electrochemical noise resistance ( Rn) and in the frequency domain using the spectral noise impedance ( Rsn). The Rsn was derived from an equivalent electrical circuit model that represented the corrosion cell implemented in the present study. These data are correlated to scanning electron microscopy (SEM) examinations and corresponding statistical analysis based on digital image analysis of the corroded surfaces. Other data used to better understand the corrosion mechanisms include the open circuit potential (OCP) and coupling-current time records. Based on statistical analysis of the pit structures for 600 and 1200 s exposures, the best fit was achieved with a 3-paramater lognormal distribution. It was observed for the 1200 s exposure that a small population of pits continued to grow beyond a threshold critical size of 10 μm. In addition, significant grain boundary attack was observed after 1200 s exposure. These data are in good agreement with the electrochemical data. Specifically, the Rn was computed to be 295 and 96 Ω-cm2 for 600 and 1200 s exposures, respectively. The calculated value of Rsn, theoretically shown to be equal to Rn in the low frequency limit, was higher than Rn for a 1200 s exposure period. However, better agreement between the Rn and Rsn was found for frequencies above 0.01 Hz. Experimental results on the measurement performance for potassium chloride (KCl) saturated double-junction Ag/AgCl and single-junction Hg/Hg2Cl2 reference electrodes in the low-pH deoxidizer solution are also compared.

  3. Solid-phase extraction of cobalt(II) from lithium chloride solutions using a poly(vinyl chloride)-based polymer inclusion membrane with Aliquat 336 as the carrier.

    PubMed

    Kagaya, Shigehiro; Cattrall, Robert W; Kolev, Spas D

    2011-01-01

    The extraction of cobalt(II) from solutions containing various concentrations of lithium chloride, hydrochloric acid, and mixtures of lithium chloride plus hydrochloric acid is reported using a poly(vinyl chloride) (PVC)-based polymer inclusion membrane (PIM) containing 40% (w/w) Aliquat 336 as a carrier. The extraction from lithium chloride solutions and mixtures with hydrochloric acid is shown to be more effective than extraction from hydrochloric acid solutions alone. The solution concentrations giving the highest amounts of extraction are 7 mol L(-1) for lithium chloride and 8 mol L(-1) lithium chloride plus 1 mol L(-1) hydrochloric acid for mixed solutions. Cobalt(II) is easily stripped from the membrane using deionized water. The cobalt(II) species extracted into the membrane are CoCl(4)(2-) for lithium chloride solutions and HCoCl(4)(-) for mixed solutions; these form ion-pairs with Aliquat 336. It is also shown that both lithium chloride and hydrochloric acid are extracted by the PIM and suppress the extraction of cobalt(II) by forming ion-pairs in the membrane (i.e. R(3)MeN(+)·HCl(2)(-) for hydrochloric acid and R(3)MeN(+)·LiCl(2)(-) for lithium chloride).

  4. Influence of Solute Content and Solidification Parameters on Grain Refinement of Aluminum Weld Metal

    NASA Astrophysics Data System (ADS)

    Schempp, Philipp; Cross, Carl Edward; Pittner, Andreas; Rethmeier, Michael

    2013-07-01

    Grain refinement provides an important possibility to enhance the mechanical properties ( e.g., strength and ductility) and the weldability (susceptibility to solidification cracking) of aluminum weld metal. In the current study, a filler metal consisting of aluminum base metal and different amounts of commercial grain refiner Al Ti5B1 was produced. The filler metal was then deposited in the base metal and fused in a GTA welding process. Additions of titanium and boron reduced the weld metal mean grain size considerably and resulted in a transition from columnar to equiaxed grain shape ( CET). In commercial pure aluminum (Alloy 1050A), the grain-refining efficiency was higher than that in the Al alloys 6082 and 5083. Different welding and solidification parameters influenced the grain size response only slightly. Furthermore, the observed grain-size reduction was analyzed by means of the undercooling parameter P and the growth restriction parameter Q, which revealed the influence of solute elements and nucleant particles on grain size.

  5. Leaching of lead from zinc leach residue in acidic calcium chloride aqueous solution

    NASA Astrophysics Data System (ADS)

    Wang, Le; Mu, Wen-ning; Shen, Hong-tao; Liu, Shao-ming; Zhai, Yu-chun

    2015-05-01

    A process with potentially reduced environmental impacts and occupational hazards of lead-bearing zinc plant residue was studied to achieve a higher recovery of lead via a cost-effective and environmentally friendly process. This paper describes an optimization study on the leaching of lead from zinc leach residue using acidic calcium chloride aqueous solution. Six main process conditions, i.e., the solution pH value, stirring rate, concentration of CaCl2 aqueous solution, liquid-to-solid (L/S) ratio, leaching temperature, and leaching time, were investigated. The microstructure and components of the residue and tailing were characterized using scanning electron microscopy (SEM) and X-ray diffraction (XRD). On the basis of experimental results, the optimum reaction conditions were determined to be a solution pH value of 1, a stirring rate of 500 r·min-1, a CaCl2 aqueous solution concentration of 400 g·L-1, a liquid-to-solid mass ratio of 7:1, a leaching temperature of 80°C, and a leaching time of 45 min. The leaching rate of lead under these conditions reached 93.79%, with an iron dissolution rate of 19.28%. Silica did not take part in the chemical reaction during the leaching process and was accumulated in the residue.

  6. Alcohol solutions of triphenyl-tetrazolium chloride as high-dose radiochromic dosimeters

    NASA Astrophysics Data System (ADS)

    Kovács, A.; Wojnárovits, L.; El-assy, N. B.; Afeefy, H. Y.; Al-Sheikhly, M.; Walker, M. L.; McLaughlin, W. L.

    1995-09-01

    The radiolytic reduction of colorless tetrazolium salts in aqueous solution to the highly colored formazan dye is a well-known acid-forming radiation chemical reaction. Radiochromic thin films and three-dimensional hydrocolloid gels have been used for imaging and mapping absorbed dose distributions. The high solubility of 2,3,5-triphenyl-tetrazolium chloride (TTC) in alcohols provides a useful liquid dosimeter (45 mM TTC in aerated ethanol) and shows a linear response of absorbance increase (λmax = 480 nm) with dose over the range 1-16 kGy. The linear molar absorption coefficient (ɛm) for the formazan at the absorption peak is 1.5 × 103 m2 mol-1, and the radiation chemical yield for the above solution is G (formazan) = 0.014 μmol J-1. The irradiation temperature coefficient is about 0.8 percent per degree Celsius rise in temperature over the temperature range 0-30 °C but is much larger between 30° and 60 °C. The unirradiated and irradiated solutions are stable over at least five days storage at normal laboratory temperature in the dark, but when stored in daylight at elevated temperature, the unirradiated solution in sealed amber glass ampoules undergoes slow photolytic dye formation, and the irradiated solution experiences initial fading and subsequent reversal (photochromism) when exposed to direct sunlight.

  7. Influence of sodium chloride content in electrolyte solution on electrochemical impedance measurements of human dentin

    PubMed Central

    Eldarrat, Aziza; High, Alec; Kale, Girish

    2017-01-01

    Background: The aim of this study was to investigate the influence of sodium chloride (NaCl) content in electrolyte solution on electrochemical impedance measurements of human dentin by employing electrochemical impedance spectroscopy. Materials and Methods: Dentin samples were prepared from extracted molars. Electrochemical impedance measurements were carried out over a wide frequency range (0.01Hz-10MHz). After measurements, samples were characterized using scanning electron microscopy. Results: Electrochemical impedance measurements showed that the mean values of dentin electrical resistance were 4284, 2062, 1336, 53 and 48kΩ at different NaCl contents in electrolyte solution. One-way ANOVA test of mean values of dentin electrical resistance revealed a significant difference (P < 0.0001) as a function of NaCl content in electrolyte solution. Comparing electrical resistance values of dentin samples at 0.05% w/v and 0.9% w/v concentrations were found to be significantly different (P < 0.05 at 95% confidence level). Scanning electron microscopy revealed structure of dentin sample with intertubular dentin matrix and distribution of patent dentinal tubules. Conclusion: This in vitro study indicated, through electrochemical impedance spectroscopy measurements, that electrical resistance of dentin was affected by the concentration of NaCl in electrolyte solution. It is clear from the current study that NaCl concentration in electrolyte solution has a marked influence on dentin electrical resistance. Therefore, this baseline data need to be considered in any future study on dental samples. PMID:28348614

  8. Thermodynamic behavior and structural properties of an aqueous sodium chloride solution upon supercooling.

    PubMed

    Corradini, D; Gallo, P; Rovere, M

    2008-06-28

    We present the results of a molecular dynamics simulation study of thermodynamic and structural properties upon supercooling of a low concentration sodium chloride solution in TIP4P water and the comparison with the corresponding bulk quantities. We study the isotherms and the isochores for both the aqueous solution and bulk water. The comparison of the phase diagrams shows that thermodynamic properties of the solution are not merely shifted with respect to the bulk. Moreover, from the analysis of the thermodynamic curves, both the spinodal line and the temperatures of maximum density curve can be calculated. The spinodal line appears not to be influenced by the presence of ions at the chosen concentration, while the temperatures of maximum density curve displays both a mild shift in temperature and a shape modification with respect to bulk. Signatures of the presence of a liquid-liquid critical point are found in the aqueous solution. By analyzing the water-ion radial distribution functions of the aqueous solution, we observe that upon changing density, structural modifications appear close to the spinodal. For low temperatures, additional modifications appear also for densities close to that corresponding to a low density configurational energy minimum.

  9. Removal of Aluminum from Leaching Solution of Lepidolite by Adding Ammonium

    NASA Astrophysics Data System (ADS)

    Li, Huan; Kuang, Ge; Hu, Song; Guo, Hui; Jin, Ran; Vekariya, Rohit L.

    2016-10-01

    Lepidolite is a kind of low-grade lithium ore (3.5-4.0% Li2O) which contains more than 22% Al2O3 and 8% K2O. Removal and utilization of the Al and K will be very important for the economic extraction of lithium from this ore. In this paper, a novel method is proposed to remove Al from the leaching solution of lepidolite by adding ammonium from (NH4)2SO4. The results indicate that adding NH4 + could remove more aluminum and have a smaller loss of lithium in comparison to adding K+ for removing aluminum in the leaching solution. The Al removal reached up to 80.44% at (K+ + NH4 +)/Al3+ molar ratio of 0.95, while the amount of Li+ (99.84%) still remained in the leaching solution. In addition, the phase equilibrium in the quaternary K2SO4-Al2(SO4)3-(NH4)2SO4-H2O system at 278.2 K was investigated to support the above conclusion. The results verify that the addition of ammonium could remove more Al3+ by easily forming potassium alum (KAl(SO4)2·12H2O) and ammonium alum (NH4Al(SO4)2·12H2O).

  10. Rheological characterization of solutions and thin films made from amylose-hexadecylammonium chloride inclusion complexes and polyvinyl alcohol

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The rheological properties of aqueous solutions and films made from blends of polyvinyl alcohol (PVOH) and amylose-hexadecylammonium chloride inclusion complexes (Hex-Am) were investigated to better understand the polymer interactions and processing parameters. Aqueous solutions of Hex-Am displayed ...

  11. Corrosion Behavior of Sputter-Deposited Aluminum-Based Alloys Exposed to Chloride Solutions.

    DTIC Science & Technology

    1987-09-30

    232 mV(SCE)J . ......................................... 19 4. The MoOX -to-AlOx ratio as a function of anodic overpotential...AC-l as a function of applied potential. Greater electropositive potentials above Eoc initially lead to an increase in the Moox (oxidized Mo) signal...followed eventually by a decrease in the concentrations of Mo in the passive film. Furthermore, the Moox /Alox (oxidized Al) ratio in the film

  12. [The influence of an isotonic solution containing benzalkonium chloride and a hypertonic seawater solution on the function of ciliary epithelium from the nasal cavity in vitro].

    PubMed

    Laberko, E L; Bogomil'sky, M R; Soldatsky, Yu L; Pogosova, I E

    2016-01-01

    The objective of the present study was to evaluate the influence of an isotonic saline solution containing benzalconium chloride and of a hypertonic seawater solution on the function of ciliary epithelium in the nasal cavity in vitro. To this effect, we investigated the cytological material obtained from 35 children presenting with adenoid tissue hypertrophy. The tissue samples were taken from the nasal cavity by the standard method. A cellular biopsy obtained from each patient was distributed between three tubes that contained isotonic saline solution supplemented by benzalconium chloride (0.1 mg/ml), a hypertonic seawater solution, and a standard physiological saline solution. It was shown that the number of the viable cells in both isotonic solutions was statistically comparable and significantly higher than in the hypertonic solution (p<0.05). The ciliary beat frequency of the cells embedded in the two isotonic solutions was not significantly different but considerably exceeded that in the hypertonic seawater solution (p<0.05). Thus, the present study has demonstrated the absence of the ciliotoxic influence of isotonic saline solution containing benzalconium chloride at a concentration of 0.1 mg/ml and the strong ciliotoxic effect of the hypertonic seawater solution. This finding gives reason to recommend isotonic solutions for the regular application whereas hypertonic solutions can be prescribed only during infectious and/or inflammatory ENT diseases.

  13. NEUTRALIZATIONS OF HIGH ALUMINUM LOW URANIUM USED NUCLEAR FUEL SOLUTIONS CONTAINING GADOLINIUM AS A NEUTRON POISON

    SciTech Connect

    Taylor-Pashow, K.

    2011-06-08

    H-Canyon will begin dissolving High Aluminum - Low Uranium (High Al/Low U) Used Nuclear Fuel (UNF) following approval by DOE which is anticipated in CY2011. High Al/Low U is an aluminum/enriched uranium UNF with small quantities of uranium relative to aluminum. The maximum enrichment level expected is 93% {sup 235}U. The High Al/Low U UNF will be dissolved in H-Canyon in a nitric acid/mercury/gadolinium solution. The resulting solution will be neutralized and transferred to Tank 39H in the Tank Farm. To confirm that the solution generated could be poisoned with Gd, neutralized, and discarded to the Savannah River Site (SRS) high level waste (HLW) system without undue nuclear safety concerns the caustic precipitation of simulant solutions was examined. Experiments were performed with three simulant solutions representative of the H-Canyon estimated concentrations in the final solutions after dissolution. The maximum U, Gd, and Al concentration were selected for testing from the range of solution compositions provided. Simulants were prepared in three different nitric acid concentrations, ranging from 0.5 to 1.5 M. The simulant solutions were neutralized to four different endpoints: (1) just before a solid phase was formed (pH 3.5-4), (2) the point where a solid phase was obtained, (3) 0.8 M free hydroxide, and (4) 1.2 M free hydroxide, using 50 wt % sodium hydroxide (NaOH). The settling behavior of the neutralized solutions was found to be slower compared to previous studies, with settling continuing over a one week period. Due to the high concentration of Al in these solutions, precipitation of solids was observed immediately upon addition of NaOH. Precipitation continued as additional NaOH was added, reaching a point where the mixture becomes almost completely solid due to the large amount of precipitate. As additional NaOH was added, some of the precipitate began to redissolve, and the solutions neutralized to the final two endpoints mixed easily and had expected

  14. Crevice corrosion of nickel superalloy in deaerated chloride/sulphate solution at 90°C

    NASA Astrophysics Data System (ADS)

    Rincón Ortiz, M.; Carranza, R. M.; Rodríguez, M. A.

    2017-01-01

    Alloy 22 is a nickel base alloy highly resistant to all forms of corrosion. It was designed to resist to most aggressive environments for industrial applications. Electrochemical studies such as Potentiodynamic-Galvanostatic-Potentiostatic (PD-GS-PD) tests and Electrochemical Impedance Spectroscopy (EIS) and Scanning Electron Microscopy (SEM) observations were performed to determine the corrosion behaviour of alloy 22 (N06022). The effect of sulphate ion in chloride containing solutions at 90°C, were studied in this work under aggressive conditions where this material might be susceptible to crevice corrosion. The electrolyte solution, which consisted of 0.1M and 1M NaCl and different sulphate concentrations. It was observed that there were complete inhibitions of crevice corrosion for R crit =[SO4 =]/[Cl-]=1 in the 0.1mol/L NaCl solutions and R crit =2 in the 1mol/L NaCl solutions. The corrosion rate obtained was about 0.1μm/year at 24 hours of immersion.

  15. Sorption of uranium(VI) ions from hydrochloric acid and ammonium chloride solutions by anion exchangers

    SciTech Connect

    Pakholkov, V.S.; Denisova, L.A.; Rychkov, V.N.; Kurnosenko, N.A.

    1988-01-01

    The sorption of macroscopic quantities of uranium from solutions of UO/sub 2/Cl/sub 2/ containing HCl and NH/sub 4/Cl in concentrations from 0.0 to 6.0 M by the AV-17 x 8, AV-16G, EDE-10P, AN-31, AN-2F, AN22, and AN-251 anion exchangers has been investigated under static conditions. The sorption isotherms are described by an equation similar to Freundlich's equation: K/sub d/ = K tilde x C/sub eq/sup 1/z/ or log K/sub d/ = log K tilde + 1/z x log C/sub eq/. Equations describing the dependence of the sorbability (or K/sub d/) on the equilibrium concentration of uranium in the solution have been obtained with the aid of the least-squares method. Conclusions regarding the chemistry of the exchange of uranium ions on anion exchangers in chloride solutions have been drawn on the basis of the UV spectra of the original solutions and the IR spectra of the ion exchangers obtained in this work, as well as the established general laws governing sorption.

  16. Reentrant condensation of lysozyme: Implications for studying dynamics of lysozyme in aqueous solutions of lithium chloride

    SciTech Connect

    Mamontov, Eugene; O'Neill, Hugh Michael

    2014-01-01

    Recent studies have outlined the use of eutectic solution of lithium chloride in water to study microscopic dynamics of lysozyme in an aqueous solvent that is remarkably similar to pure water in many respects, yet allows experiments over a wide temperature range without the solvent crystallization. The eutectic point in (H2O)R(LiCl) system corresponds to R 7.3, and it is of interest to investigate whether less concentrated aqueous solutions of LiCl could be employed in low-temperature studies of a solvated protein. We have investigated a range of concentrations of lysozyme and LiCl in aqueous solutions to identify systems that do not show phase separation and avoid solvent crystallization on cooling down. Compared to the lysozyme concentration in solution, the concentration of LiCl in the aqueous solvent plays the major role in determining systems suitable for low-temperature studies. We have observed interesting and rich phase behavior reminiscent of reentrant condensation of proteins.

  17. Cyclic stress effect on stress corrosion cracking of duplex stainless steel in chloride and caustic solutions

    NASA Astrophysics Data System (ADS)

    Yang, Di

    Duplex stainless steel (DSS) is a dual-phase material with approximately equal volume amount of austenite and ferrite. It has both great mechanical properties (good ductility and high tensile/fatigue strength) and excellent corrosion resistance due to the mixture of the two phases. Cyclic loadings with high stress level and low frequency are experienced by many structures. However, the existing study on corrosion fatigue (CF) study of various metallic materials has mainly concentrated on relatively high frequency range. No systematic study has been done to understand the ultra-low frequency (˜10-5 Hz) cyclic loading effect on stress corrosion cracking (SCC) of DSSs. In this study, the ultra-low frequency cyclic loading effect on SCC of DSS 2205 was studied in acidified sodium chloride and caustic white liquor (WL) solutions. The research work focused on the environmental effect on SCC of DSS 2205, the cyclic stress effect on strain accumulation behavior of DSS 2205, and the combined environmental and cyclic stress effect on the stress corrosion crack initiation of DSS 2205 in the above environments. Potentiodynamic polarization tests were performed to investigate the electrochemical behavior of DSS 2205 in acidic NaCl solution. Series of slow strain rate tests (SSRTs) at different applied potential values were conducted to reveal the optimum applied potential value for SCC to happen. Room temperature static and cyclic creep tests were performed in air to illustrate the strain accumulation effect of cyclic stresses. Test results showed that cyclic loading could enhance strain accumulation in DSS 2205 compared to static loading. Moreover, the strain accumulation behavior of DSS 2205 was found to be controlled by the two phases of DSS 2205 with different crystal structures. The B.C.C. ferrite phase enhanced strain accumulation due to extensive cross-slips of the dislocations, whereas the F.C.C. austenite phase resisted strain accumulation due to cyclic strain

  18. Early effects of aluminum chloride on beta-secretase mRNA expression in a neuronal model of beta-amyloid toxicity.

    PubMed

    Castorina, Alessandro; Tiralongo, Adriana; Giunta, Salvatore; Carnazza, Maria Luisa; Scapagnini, Giovanni; D'Agata, Velia

    2010-08-01

    Amyloid beta peptide (Abeta), generated by proteolytic cleavage of the amyloid precursor protein (APP), plays a pivotal role in the pathogenesis of Alzheimer's disease (AD). The key step in the generation of Abeta is cleavage of APP by beta-secretases (beta-site APP-cleaving enzyme 1 (BACE1) and BACE2). There has been suggestion of interaction between aluminum and several AD-associated pathways. However, the underlying mechanisms still remain unclear. Here, we report the effects of aluminum chloride (AlCl(3)) in Abeta-induced toxicity using differentiated neuronal SH-SY5Y cells. The metal significantly enhances Abeta-induced cell death at concentrations ranging from 50 to 300 microM after 24 and 48 h. After 72 and 96 h treatment, cell death is increased already at 10 microM. Early coexposure of cells to 10 microM AlCl(3) and 2 microM Abeta differentially affected beta-secretase mRNA levels as compared to single Abeta treatment after 1 and 3 h. BACE1 levels were slightly reduced after 1 h and significantly increased after 3 h exposure, whereas BACE2 levels were increased at both times considered. Both genes' mRNA levels were downregulated at longer times (6, 12, and 24 h). Although these results indicate that aluminum toxicity is correlated to changes in both BACE1 and BACE2 expression levels, the subsequent common downregulation observed suggests that aluminum involvement in the Abeta cascade is subtle, and other underlying mechanisms might be involved.

  19. Interfacial behavior of perchlorate versus chloride ions in saturated aqueous salt solutions

    SciTech Connect

    Ghosal, S; Kuo, I W; Baer, M D; Bluhm, H

    2009-04-14

    In recent years combination of theoretical and experimental work have presented a novel view of the aqueous interface wherein hard and/or multiply charged ions are excluded from the interface, but large polarizable anions show interfacial enhancement relative to the bulk. The observed trend in the propensity of anions to adsorb at the air/water interface appears to be reverse of the Hofmeister series for anions. This study focuses on experimental and theoretical examination of the partitioning behavior of perchlorate (ClO{sub 4}{sup -}) and chloride (Cl{sup -}) ions at the air/water interface. We have used ambient pressure X-ray photoelectron spectroscopy technique to directly probe the interfacial concentrations of ClO{sub 4}{sup -} and Cl{sup -} ions in sodium perchlorate and sodium chloride solutions, respectively. Experimental observations are compared with first principles molecular dynamics simulations. Both experimental and simulation results show enhancement of ClO{sub 4}{sup -} ion at the interface, compared with the absence of such enhancement in the case of Cl{sup -} ion. These observations are in agreement with the expected trend in the interfacial propensity of anions based on the Hofmeister series.

  20. Protection of copper surface with phytic acid against corrosion in chloride solution.

    PubMed

    Peca, Dunja; Pihlar, Boris; Ingrid, Milošev

    2014-01-01

    Phytic acid (inositol hexaphosphate) was tested as a corrosion inhibitor for copper in 3% sodium chloride. Phytic acid is a natural compound derived from plants, it is not toxic and can be considered as a green inhibitor. Electrochemical methods of linear polarization and potentiodynamic polarization were used to study the electrochemical behaviour and evaluate the inhibition effectiveness. To obtain the optimal corrosion protection the following experimental conditions were investigated: effect of surface pre-treatment (abrasion and three procedures of surface roughening), pre-formation of the layer of phytic acid, time of immersion and concentration of phytic acid. To evaluate the surface pre-treatment procedures the surface roughness and contact angle were measured. Optimal conditions for formation of phytic layer were selected resulting in the inhibition effectiveness of nearly 80%. Morphology and composition of the layer were further studied by scanning electron microscopy, energy dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy. The layer of phytic acid with thickness in the nanometer range homogeneously covers the copper surface. The obtained results show that this natural compound can be used as a mildly effective corrosion inhibitor for copper in chloride solution.

  1. Electrochemical treatment of Orange II dye solution--use of aluminum sacrificial electrodes and floc characterization.

    PubMed

    Mollah, M Yousuf A; Gomes, Jewel A G; Das, Kamol K; Cocke, David L

    2010-02-15

    Electrocoagulation (EC) of Orange II dye in a flow through cell with aluminum as sacrificial electrodes was carried out under varying conditions of dye concentration, current density, flow rate, conductivity, and the initial pH of the solution in order to optimize the operating parameters for maximum benefits. Maximum removal efficiency of 94.5% was obtained at the following conditions: dye concentration=10 ppm, current density=160 A/m(2), initial pH 6.5, conductance=7.1 mS/cm, flow rate=350 mL/min, and concentration of added NaCl=4.0 g/L of dye solution. The EC-floc was characterized using Fourier transform infrared spectroscopy, scanning electron microscopy/energy dispersive X-ray spectroscopy, and powder X-ray diffraction techniques. The removal mechanism has been proposed that is in compliance with the Pourbaix diagram, solubility curve of aluminum oxides/hydroxides, and physico-chemical properties of the EC-floc.

  2. Generalized chloride mass balance: Forward and inverse solutions for one-dimensional tracer convection under transient flux

    SciTech Connect

    Ginn, T.R.; Murphy, E.M.

    1996-12-01

    Forward and inverse solutions are provided for analysis of inert tracer profiles resulting from one-dimensional convective transport under fluxes which vary with time and space separately. The developments are displayed as an extension of conventional chloride mass balance (CMB) techniques to account for transient as well as space-dependent water fluxes. The conventional chloride mass balance has been used over two decades to estimate recharge over large time scales in arid environments. In this mass balance approach, the chloride concentration in the pore water, originating from atmospheric fallout, is inversely proportional to the flux of water through the sediments. The CMB method is especially applicable to arid and semi-arid regions where evapotranspirative enrichment of the pore water produces a distinct chloride profile in the unsaturated zone. The solutions presented allow incorporation of transient fluxes and boundary conditions in CMB analysis, and allow analysis of tracer profile data which is not constant with depth below extraction zone in terms of a rational water transport model. A closed-form inverse solution is derived which shows uniqueness of model parameter and boundary condition (including paleoprecipitation) estimation, for the specified flow model. Recent expressions of the conventional chloride mass balance technique are derived from the general model presented here; the conventional CMB is shown to be fully compatible with this transient flow model and it requires the steady-state assumption on chloride mass deposition only (and not on water fluxes or boundary conditions). The solutions and results are demonstrated on chloride profile data from west central New Mexico.

  3. Equilibrium studies of cobalt(II) extraction with 2-pyridineketoxime from mixed sulphate/chloride solution.

    PubMed

    Wieszczycka, Karolina; Krupa, Marta; Wojciechowska, Aleksandra; Wojciechowska, Irmina; Olszanowski, Andrzej

    In present paper the equilibrium of cobalt extraction with 1-(2-pyridyl)tridecan-1-one oxime from the chloride/sulphate solutions was studied. The presented results indicated that extraction depends on a number of process variables, including the pH, metal and Cl(-) concentration in the aqueous feed, and concentration of the oxime in the organic phase. The created cobalt-complexes with the 2-pyridine ketoxime were stable and only concentrated HCl was found to be a suitable stripping agent for coordinated metal. The separation of Co(II) from Zn(II), Ni(II) and Cu(II) was also studied, but the selective recovery of the metals was possible using the multi-stage stripping process.

  4. A method of calculating quartz solubilities in aqueous sodium chloride solutions

    USGS Publications Warehouse

    Fournier, R.O.

    1983-01-01

    The aqueous silica species that form when quartz dissolves in water or saline solutions are hydrated. Therefore, the amount of quartz that will dissolve at a given temperature is influenced by the prevailing activity of water. Using a standard state in which there are 1,000 g of water (55.51 moles) per 1,000 cm3 of solution allows activity of water in a NaCl solution at high temperature to be closely approximated by the effective density of water, pe, in that solution, i.e. the product of the density of the NaCl solution times the weight fraction of water in the solution, corrected for the amount of water strongly bound to aqueous silica and Na+ as water of hydration. Generally, the hydration of water correction is negligible. The solubility of quartz in pure water is well known over a large temperature-pressure range. An empirical formula expresses that solubility in terms of temperature and density of water and thus takes care of activity coefficient and pressure-effect terms. Solubilities of quartz in NaCl solutions can be calculated by using that equation and substituting pe, for the density of pure water. Calculated and experimentally determined quartz solubilities in NaCl solutions show excellent agreement when the experiments were carried out in non-reactive platinum, gold, or gold plus titanium containers. Reactive metal containers generally yield dissolved silica concentrations higher than calculated, probably because of the formation of metal chlorides plus NaOH and H2. In the absence of NaOH there appears to be no detectable silica complexing in NaCl solutions, and the variation in quartz solubility with NaCl concentration at constant temperature can be accounted for entirely by variations in the activity of water. The average hydration number per molecule of dissolved SiO2 in liquid water and NaCl solutions decreases from about 2.4 at 200??C to about 2.1 at 350??C. This suggests that H4SiO4 may be the dominant aqueous silica species at 350??C, but other

  5. Solid solution barium–strontium chlorides with tunable ammonia desorption properties and superior storage capacity

    SciTech Connect

    Bialy, Agata; Blanchard, Didier; Vegge, Tejs; Quaade, Ulrich J.

    2015-01-15

    Metal halide ammines are very attractive materials for ammonia absorption and storage—applications where the practically accessible or usable gravimetric and volumetric storage densities are of critical importance. Here we present, that by combining advanced computational materials prediction with spray drying and in situ thermogravimetric and structural characterization, we synthesize a range of new, stable barium-strontium chloride solid solutions with superior ammonia storage densities. By tuning the barium/strontium ratio, different crystallographic phases and compositions can be obtained with different ammonia ab- and desorption properties. In particular it is shown, that in the molar range of 35–50% barium and 65–50% strontium, stable materials can be produced with a practically usable ammonia density (both volumetric and gravimetric) that is higher than any of the pure metal halides, and with a practically accessible volumetric ammonia densities in excess of 99% of liquid ammonia. - Graphical abstract: Thermal desorption curves of ammonia from Ba{sub x}Sr{sub (1−x)}Cl{sub 2} mixtures with x equal to 0.125, 0.25 and 0.5 and atomic structure of Sr(NH{sub 3}){sub 8}Cl{sub 2}. - Highlights: • Solid solutions of strontium and barium chloride were synthesized by spray drying. • Adjusting molar ratios led to different crystallographic phases and compositions. • Different molar ratios led to different ammonia ab-/desorption properties. • 35–50 mol% BaCl{sub 2} in SrCl{sub 2} yields higher ammonia density than any other metal halide. • DFT calculations can be used to predict properties of the mixtures.

  6. Formation of aqueous solutions on Mars via deliquescence of chloride-perchlorate binary mixtures

    NASA Astrophysics Data System (ADS)

    Gough, R. V.; Chevrier, V. F.; Tolbert, M. A.

    2014-05-01

    Perchlorate salts, known to exist on Mars, can readily absorb water vapor and deliquesce into aqueous solutions even at low temperatures. The multiple soluble ionic species, such as chloride salts, present in the Martian subsurface may affect this deliquescence. Here we study the deliquescence (solid to aqueous transition) and efflorescence (aqueous to solid transition) of three perchlorate/chloride mixtures: KClO4/KCl at 253 K, NaClO4/NaCl at 243 and 253 K, and Mg(ClO4)2/MgCl2 at 243 and 253 K. A Raman microscope with an environmental cell was used to monitor the phase transitions of internally mixed ClO-4/Cl- particles as a function of the perchlorate mole fraction. The eutonic relative humidity (where deliquescence begins to occur regardless of ClO-4 mole fraction), deliquescence relative humidity (DRH, where complete deliquescence occurs), and efflorescence relative humidity (ERH) were measured for several perchlorate mole ratios for each cation system. At the temperatures studied, the eutonic relative humidity was measured to be 28% RH for Mg(ClO4)2/MgCl2 mixtures, 38% RH for NaClO4/NaCl mixtures, and 82% RH for KClO4/KCl mixtures. The DRH depends on the perchlorate mole ratio, but is below the DRH of the least deliquescent (highest DRH) pure salt. When humidity is lowered around an aqueous salt mixture, we find that efflorescence occurs at an RH below the DRH due to the kinetic inhibition of crystallization. The ERH values of the salt solutions were as low as 5% RH for Mg(ClO4)2/MgCl2 mixtures, as low as 13% RH for NaClO4/NaCl mixtures, and as low as 66% RH for KClO4/KCl mixtures. The low eutonic RH values for the Na+ and Mg2+ perchlorate/chloride mixtures are important: wherever Mg(ClO4)2 and MgCl2 or NaClO4 and NaCl coexist at the temperatures studied, mixtures will contain a stable aqueous phase above 28 or 38% RH, respectively, regardless of the perchlorate mole fraction. This liquid water may persist until 5 or 13% RH, respectively.

  7. Mercury adsorption on granular activated carbon in aqueous solutions containing nitrates and chlorides.

    PubMed

    Di Natale, F; Erto, A; Lancia, A; Musmarra, D

    2011-09-15

    Adsorption is an effective process to remove mercury from polluted waters. In spite of the great number of experiments on this subject, the assessment of the optimal working conditions for industrial processes is suffering the lack of reliable models to describe the main adsorption mechanisms. This paper presents a critical analysis of mercury adsorption on an activated carbon, based on the use of chemical speciation analysis to find out correlations between mercury adsorption and concentration of dissolved species. To support this analysis, a comprehensive experimental study on mercury adsorption at different mercury concentrations, temperatures and pH was carried out in model aqueous solutions. This study pointed out that mercury capture occurs mainly through adsorption of cationic species, the adsorption of anions being significant only for basic pH. Furthermore, it was shown that HgOH(+) and Hg(2+) are captured to a higher extent than HgCl(+), but their adsorption is more sensitive to solution pH. Tests on the effect of temperature in a range from 10 to 55 °C showed a peculiar non-monotonic trend for mercury solution containing chlorides. The chemical speciation and the assumption of adsorption exothermicity allow describing this experimental finding without considering the occurrence of different adsorption mechanisms at different temperature.

  8. The solubility of ozone and kinetics of its chemical reactions in aqueous solutions of sodium chloride

    NASA Astrophysics Data System (ADS)

    Levanov, A. V.; Kuskov, I. V.; Antipenko, E. E.; Lunin, V. V.

    2008-12-01

    The solubility of ozone and the kinetics of its decomposition and interaction with chloride ions in a 1 M aqueous solution of NaCl at 20°C and pH 8.4-10.8 were studied. The ratio between the concentration of O3 in solution and the gas phase was found to be 0.16 at pH 8.4-9.8. The concentration of dissolved ozone decreased sharply as pH increased to 10.8 because of a substantial increase in the rate of its decomposition. It was observed for the first time that the interaction of O3 with Cl- in alkaline media resulted in the formation of ClO{3/-} chlorate ions. The dependence of the rate of formation of ClO{3/-} on pH was determined; its maximum value was found to be 9.6 × 10-6 mol l-1 min-1 at pH 10.0 and the concentration of ozone at the entrance of the reactor 30.0 g/m3. A spectrophotometric method for the determination of chlorate ions (concentrations 1 × 10-5-3 × 10-4 M) in aqueous solutions was suggested.

  9. A study of the electrochemical behavior in tungsten and caustic solutions and platinum/iridium in chloride solutions, informal report

    SciTech Connect

    Vitus, C.M.; Isaacs, H.S.; Schroeder, V.

    1994-11-22

    Platinum/iridium and tungsten wires were electronically etched in chloride and caustic solution, respectively, to produce tips with high aspect ratio. A direct relationship between the meniscus and the aspect ratio of etched tips was established. Scanning electron micrographs indicated that higher aspect ratios were obtained by changing the geometry of the meniscus during the etch either by an increase in the applied a.c. voltage or with the addition of a nonpolar layer above the electrolytic solution during the etching process. Above the breakdown voltage, two possible mechanisms appeared to control the etching process by expediting chemical dissolution: cavitation and sparking. Cavitation caused erosion due to the force of evolved gases against the electrode and sparking attacked the surface by vaporizing the metal. Sparking commenced on both wires near 24V. This voltage corresponded to a minimum in the plot of total etch time versus voltage. From light emission studies, sparking on Pt/Ir was associated with the ionization of Pt, Ir, Ca, and Cl. A compositional analysis of insoluble black particles produced during a.c. and d.c. etching of Pt/Ir revealed Pt and Ir as the major constituents of the product. The sparking process was shown to have a potential use in micromachining.

  10. Spectrophotometric determination of the stability of tin(II) chloride complexes in aqueous solution up to 300°C

    NASA Astrophysics Data System (ADS)

    Müller, B.; Seward, T. M.

    2001-11-01

    The aim of this study was to gain insight into the aqueous chemistry of tin at elevated temperatures and pressures. For this purpose, the spectra of chloridotin(II) complexes in the ultraviolet region were measured in acid chloride solutions containing 1.00 × 10 -4 m tin, 1.00 × 10 -2 m HCl and varying NaCl concentrations up to 2.936 m from 25 to 300°C and at the equilibrium saturated vapor pressure of the system. The thermodynamic cumulative and stepwise formation constants of the individual tin(II) chloride species were calculated from the spectrophotometric data using a nonlinear least squares routine. At 25°C, a scheme including five species of SnCl n2-n (0 ≤ n ≤ 4) best fitted the available data. At 300°C however, SnCl 20 and SnCl 3- are the predominant species at total chloride concentrations >0.1 m. The presence of SnCl 42- in concentrated (up to 3 m) chloride solutions was not detected above 150°C. With increasing temperature, chloridotin(II) complex stability is characterized by quite large endothermic enthalpies and large positive entropies of formation. It was concluded that tin(II) chloride complexes could be important in the transport and deposition of tin by hydrothermal ore solutions of moderate to high salinity.

  11. Outer-sphere interaction of aluminum and gallium solvates with competitive anions in 1,2-propanediol solutions

    SciTech Connect

    Petrosyants, S.P.; Buslaeva, E.R.

    1986-04-01

    The interaction of aluminum and gallium solvates with ..pi..-acid ligand in 1,2-propanediol solutions has been investigated. The formation of associates of hexacoordinate aluminum solvates depends on the solvation of the anions in the bulk of the solution or on the faces of the solvento complexes. In the case of gallium the association of the solvates with the anions is determined by two factors: the existence of a configurational equilibrium for the solvento complexes and the preferential solvation of the competitive ..pi..-acid ligands.

  12. Solution Equilibria between Aluminum(III) Ion and L-histidine or L-tyrosine

    PubMed Central

    Jelic, Ratomir; Dzajevic, Dragana; Cvijovic, Mirjana

    2002-01-01

    Toxic effects due to high aluminum body loads were observed in a number of conditions following ingestion of Al-containing antacids. Bio-availability of aluminum depends not only on the solubility of the ingested salt but also on the physico-chemical properties of the soluble Al complexes formed in body fluids. Amino acids may, upon interaction with Al-salts, form absorbable Al-complexes. Hence, complex formation equilibria between Al3+ and either, L- histidine or L-tyrosine were studied by glass electrode potentiometric (0.1 mol/L LiCl ionic medium, 298 K), proton NMR and uv spectrophotometric measurements. Non linear least squares treatment of the potentiometric data indicates that in the concentration ranges: 0.5≤CA1≤2.0 ; 1.0≤CHis≤10.0; 2.5≤PH≤6.5, in Al3+ + His solutions, the following complexes (with log overall stability constants given in parenthesis) are formed: Al(HHis)3+(12.21±0.08); Al(His)2+, (7.25±0.08); and Al(HHis)His2+, (20.3±0.1). In Al3+ + Tyr solutions in the concentration range 1.0≤CTyr≤3.0 mmol/L and ligand to metal concentration ratio from 2:1 to 3:1, in the pH interval from 3.0 to 6.5 the formation of the following complexes was detected: Al(HTyr)2+, (12.72±0.09); Al(Tyr)2+, (10.16±0.03) and Al(OH)2Tyr , (2.70±0.05). Proton NMR data indicate that in Al(His)2+ complex histidine acts as a monodentate ligand but its bidentate coordination is possible with carboxylate oxygen and imidazole 1-nitrogen as donors. In Al(HTyr)3+ complex tyrosine is a monodentate ligand with carboxylate oxygen as donor. The mechanism of the formation of complexes in solution is discussed as well as their possible role in aluminum toxicity. PMID:18476000

  13. Surface Characterization of 7075-T73 Aluminum Exposed to Anodizing Pretreatment Solutions

    NASA Astrophysics Data System (ADS)

    Savas, Terence P.; Earthman, James C.

    2008-10-01

    Localized corrosion damage in Type 7075-T73 aluminum alloy was investigated for various anodizing pretreatment solutions. The postexposure surface corrosion was characterized by use of scanning electron microscopy (SEM) examination. In addition, SEM and energy dispersive spectroscopy (EDS) were used for second-phase (constituent) particle identification for those found to induce pitting corrosion during solution exposure. The pitting mechanisms were identified as circumferential where the particles are noble with respect to the matrix phase and by selective dissolution where they are anodic. The designated category-1 degreasing and category-2 inhibited alkaline solutions did not initiate localized corrosion after 1200 s exposures. However, the category-3 high-pH NaOH and category-4 low-pH HNO3 based solutions were found to initiate pitting attack, with the NaOH being significantly more aggressive. It was hypothesized that if the pits initiating during the pretreatment exposures were beyond a threshold size, on the order of 10-20 μm, a higher current density existed at these locations during subsequent electrochemical processes, thus resulting in larger and deeper pit structures. These surface defects are of primary concern with respect to accelerated fatigue crack nucleation. For smaller pits, on the order of 1-5 μm, the anodic process had a smoothing affect where the film growth tended to passivate the pits.

  14. Aluminum Exposure in Neonatal Patients Using the Least Contaminated Parenteral Nutrition Solution Products

    PubMed Central

    Poole, Robert L.; Pieroni, Kevin P.; Gaskari, Shabnam; Dixon, Tessa; Kerner, John A.

    2012-01-01

    Aluminum (Al) is a contaminant in all parenteral nutrition (PN) solution component products. Manufacturers currently label these products with the maximum Al content at the time of expiry. We recently published data to establish the actual measured concentration of Al in PN solution products prior to being compounded in the clinical setting [1]. The investigation assessed quantitative Al content of all available products used in the formulation of PN solutions. The objective of this study was to assess the Al exposure in neonatal patients using the least contaminated PN solutions and determine if it is possible to meet the FDA “safe limit” of less than 5 μg/kg/day of Al. The measured concentrations from our previous study were analyzed and the least contaminated products were identified. These concentrations were entered into our PN software and the least possible Al exposure was determined. A significant decrease (41%–44%) in the Al exposure in neonatal patients can be achieved using the least contaminated products, but the FDA “safe limit” of less than 5 μg/kg/day of Al was not met. However, minimizing the Al exposure may decrease the likelihood of developing Al toxicity from PN. PMID:23201834

  15. Structural properties of the inner coordination sphere of indium chloride complexes in organic and aqueous solutions.

    PubMed

    Narita, Hirokazu; Tanaka, Mikiya; Shiwaku, Hideaki; Okamoto, Yoshihiro; Suzuki, Shinichi; Ikeda-Ohno, Atsushi; Yaita, Tsuyoshi

    2014-01-28

    The nature of the inner coordination sphere of In(3+) present in both the organic and aqueous solutions during the solvent extraction of In(3+) from an aqueous HCl solution with tri-n-octyl amine (TOA) was investigated by In K-edge XAFS. This information was then used to clarify the details of the extraction properties of indium chloride anion complexes with TOA. In aqueous HCl solution (0.1-10 M), In(3+) exists as octahedral anion complexes, [InCln(H2O)6-n](3-n) (n ≥ 4); the [InCl6](3-) complex is dominant at 10 M HCl. The extraction of In(3+) from HCl solution with TOA was performed using two kinds of diluents: nitrobenzene (NB) or n-dodecane (DD), which contained 20 vol% of 2-ethylhexanol as an additive. The stoichiometric composition of the extracted complexes, which is estimated from the distribution ratios of In(3+), is affected by the diluents and the HCl concentration of the aqueous phase; the apparent values of TOA/In(3+) in the extracted complex are 3 for DD-1 M HCl (diluent-aqueous phase) and DD-5 M HCl, 2 for NB-1 M HCl and NB-5 M HCl, and 1 for NB-10 M HCl. The EXAFS analysis of these extracted complexes shows that the In(3+) has ∼4 Cl(-) at ∼2.336 Å and no H2O in the inner coordination sphere; additionally, the shape of the XANES suggests that their coordination geometry is tetrahedral. Therefore, the same tetrahedral [InCl4](-) complex is formed during the extraction in spite of the variation in the stoichiometric composition (TOA/In(3+) = 1-3) of the extracted complexes.

  16. Peptide-based biocoatings for corrosion protection of stainless steel biomaterial in a chloride solution.

    PubMed

    Muruve, Noah G G; Cheng, Y Frank; Feng, Yuanchao; Liu, Tao; Muruve, Daniel A; Hassett, Daniel J; Irvin, Randall T

    2016-11-01

    In this work, PEGylated D-amino acid K122-4 peptide (D-K122-4-PEG), derived from the type IV pilin of Pseudomonas aeruginosa, coated on 304 stainless steel was investigated for its corrosion resistant properties in a sodium chloride solution by various electrochemical measurements, surface characterization and molecular dynamics simulation. As a comparison, stainless steel electrodes coated with non-PEGylated D-amino acid retroinverso peptide (RI-K122-4) and D-amino acid K122-4 peptide (D-K122-4) were used as control variables during electrochemical tests. It was found that the D-K122-4-PEG coating is able to protect the stainless steel from corrosion in the solution. The RI-K122-4 coating shows corrosion resistant property and should be investigated further, while the D-K122-4 peptide coating, in contrast, shows little to no effect on corrosion. The morphological characterizations support the corrosion resistance of D-K122-4-PEG on stainless steel. The adsorption of D-K122-4 molecules occurs preferentially on Fe2O3, rather than Cr2O3, present on the stainless steel surface.

  17. Optimized atomistic force fields for aqueous solutions of Magnesium and Calcium Chloride: Analysis, achievements and limitations

    NASA Astrophysics Data System (ADS)

    Elfgen, Roman; Hülsmann, Marco; Krämer, Andreas; Köddermann, Thorsten; Kirschner, Karl N.; Reith, Dirk

    2016-10-01

    Molecular simulations are an important tool in the study of aqueous salt solutions. To predict the physical properties accurately and reliably, the molecular models must be tailored to reproduce experimental data. In this work, a combination of recent global and local optimization tools is used to derive force fields for MgCl2 (aq) and CaCl2 (aq). The molecular models for the ions are based on a Lennard-Jones (LJ) potential with a superimposed point charge. The LJ parameters are adjusted to reproduce the bulk density and shear viscosity of the different solutions at 1 bar and temperatures of 293.15, 303.15, and 318.15 K. It is shown that the σ-value of chloride consistently has the strongest influence on the system properties. The optimized force field for MgCl2 (aq) provides both properties in good agreement with the experimental data over a wide range of salt concentrations. For CaCl2 (aq), a compromise was made between the bulk density and shear viscosity, since reproducing the two properties requires two different choices of the LJ parameters. This is demonstrated by studying metamodels of the simulated data, which are generated to visualize the correlation between the parameters and observables by using projection plots. Consequently, in order to derive a transferable force field, an error of ˜3% on the bulk density has to be tolerated to yield the shear viscosity in satisfactory agreement with experimental data.

  18. Analysis of antibacterial efficacy of plasma-treated sodium chloride solutions

    NASA Astrophysics Data System (ADS)

    Hänsch, Mareike A. C.; Mann, Miriam; Weltmann, Klaus-Dieter; von Woedtke, Thomas

    2015-11-01

    In this study, the change of chemical composition of sodium chloride solutions (NaCl, 0.85%) induced by non-thermal atmospheric pressure plasma (APP) treatment and subsequent effects on bacteria (Escherichia coli) are investigated. Besides acidification caused by APP, hydrogen peroxide (H2O2), nitrite (\\text{NO}2- ), and nitrate (\\text{NO}3- ) are generated as stable end-products of various chemical reactions in APP-treated liquids. Inactivation kinetics and reduction factors were recorded for E. coli (K12). Almost identical antimicrobial effects were observed with both direct APP exposure to bacteria suspension and exposure of APP-treated liquids to bacteria (indirect treatment). Consequently, main bactericidal effects are caused by chemical reactions which are mediated via the liquid phase. Moreover, APP-treated liquids have shown long-term activity (30 min) that possibly correlates with the ratio of \\text{NO}2- /H2O2. Therefore, \\text{NO}2- and H2O2 are identified as key agents for antimicrobial short- and long-term effects, respectively. The antimicrobial stability observed is strongly dependent on the used treatment regime and correlates additionally with the altered chemical composition of APP-treated liquids. Besides these effects, it was also shown that bacteria do not acquire resistance to such APP-treated solutions.

  19. Catalytic destruction of perchlorate in ferric chloride and hydrochloric acid solution with control of temperature, pressure and chemical reagents

    DOEpatents

    Gu, Baohua; Cole, David R.; Brown, Gilbert M.

    2004-10-05

    A method is described to decompose perchlorate in a FeCl.sub.3 /HCl aqueous solution such as would be used to regenerate an anion exchange resin used to remove perchlorate. The solution is mixed with a reducing agent, preferably an organic alcohol and/or ferrous chloride, and can be heated to accelerate the decomposition of perchlorate. Lower temperatures may be employed if a catalyst is added.

  20. Local toxicity of benzalkonium chloride in ophthalmic solutions following repeated applications.

    PubMed

    Okahara, Akihiko; Kawazu, Kouichi

    2013-01-01

    We performed repeated toxicity studies of benzalkonium chloride (BAK)-containing vehicles of ophthalmic solutions in monkeys and rabbits to assess the local toxicity of BAK after repeated applications on the ocular surface. Local toxicity of BAK was evaluated by toxicity studies in which a 0.01% BAK-containing vehicle was applied twice/day for 52 weeks, 4 times/day for 39 weeks, or 6 times/day for 13 weeks, or in which a 0.005% BAK-containing vehicle was applied 6 times/day for 52 weeks or twice/day for 4 weeks in monkeys. Local toxicity of BAK was also evaluated where a 0.01% BAK-containing vehicle was applied 6 times/day for 6 weeks, or a 0.005% BAK-containing vehicle was applied twice/day for 39 weeks or 8 times/day for 4 weeks in rabbits. These doses were chosen because BAK is generally used at concentrations up to 0.01% in ophthalmic solutions. The BAK-containing vehicle did not cause ophthalmological changes suggestive of irritation, allergy, or corneal damage. We also did not observe any histopathological changes in the eyeball, eyelid, lacrimal gland, and nasal cavity, with repeated applications of BAK for up to 52 weeks, up to 8 times/day, or at concentrations up to 0.01%, in monkeys and rabbits. Our results suggest that BAK in concentrations up to 0.01% in ophthalmic solution is non-toxic to the eyeball, its accessory organs, and the nasal cavity after long repeated applications.

  1. Benzodiazepine effects on licking responses for sodium chloride solutions in water-deprived male rats.

    PubMed

    Cooper, Steven J; Higgs, Suzanne

    2005-06-30

    The aim of this study was to investigate, for the first time, the effects of a centrally active benzodiazepine receptor agonist, midazolam maleate, on the microstructure of licking responses for a range of sodium chloride (NaCl) solutions in mildly water-deprived male rats. Doses of midazolam were chosen (0.3-3.0 mg/kg. i.p.) which have been characterised in studies of licking responses for several different kinds of nutrients. NaCl concentrations (0.075 M-0.45 M) were chosen to cover a range of taste preferences and acceptability. A brief-contact testing session was employed to focus on the initial determinants of licking responses (i.e. taste palatability), and to minimise any contribution of post-ingestional effects. The results indicate the midazolam significantly increased the total number of licks recorded across all salt concentrations, but that it had no effect on the number of bouts of licking. Instead, midazolam specifically enhanced the mean duration of licking bouts, an effect that was most evident at the weaker but more acceptable NaCl concentrations (0.075 M and 0.15 M). In addition, midazolam diminished the intrabout rate of licking across all salt concentrations. These results confirm that benzodiazepines can exert a specific pattern of effects on the microstructure of licking for salt solutions. They are discussed in terms of the oropharyngeal stimulation controlling intake and the palatability or "liking" hypothesis for the effects of benzodiazepines on taste stimuli, and indicate that the hypothesis is applicable to salt solution ingestive behaviour.

  2. Composition and structure of Pt chloride complexes in hydrothermal solutions, according to X-ray absorption spectroscopy

    NASA Astrophysics Data System (ADS)

    Tagirov, B. R.; Trigub, A. L.; Selivanov, P. V.; Koroleva, L. A.

    2017-03-01

    The local atomic environment of Pt in chloride solutions is studied at 25 and 300-350°C via X-ray absorption spectroscopy. A comparison of the Pt L 3-edge XANES spectra for aqueous chloride solutions and reference compounds (K2PtCl4 and K2PtCl6) shows that platinum is in oxidation state +2 at all temperatures, and the complex composition remains unchanged in the experimental range of temperatures (25-350°C) and solution compositions ( m(Cltot) > 0.4 mol kg-1 of H2O). Based on EXAFS spectral analysis, the composition of the complex being dominant in chloride solutions is found to be PtCl4 2- with interatomic Pt-Cl distances of 2.31 ± 0.01 Å, regardless of the temperature. It is concluded that the local environments of Pt and Pd in hydrothermal solutions are similar, and the main form of transfer for these metals is a square-planar complex with four Cl ligands and identical interatomic distances.

  3. Formation of palladium(II) hydroxychloride complexes and precipitates in sodium chloride solutions and seawater

    NASA Astrophysics Data System (ADS)

    Byrne, Robert H.; Yao, Wensheng

    2000-12-01

    Spectrophotometric measurements of Pd(II) in 0.5 M NaCl indicate that the PdCl3OH2- formation constant at 25°C is ClK∗1 = [PdCl3OH2-][H+][Cl-][PdCl42-]-1 = 10-8.98. This constant is more than two orders of magnitude smaller than previous results derived through solubility analysis. Kinetic experiments indicate that equilibration between PdCl42- and PdCl3OH2- is complete in less than one second. The discrepancy between depictions of Pd(II) speciation obtained by using spectrophotometric and solubility analysis is apparently caused by the formation of mixed hydroxychloride solid phases (PdClaOH2-a), rather than pure Pd(OH)2(s), when Pd(OH)2(s) is equilibrated in concentrated chloride solutions at high pH. In Pd(II) solubility analysis, and solubility analyses of other strongly hydrolyzed metals in seawater, the composition of the solid phase must be carefully examined for appropriate deconvolution of data.

  4. Biochemical characterization of a Pseudomonas fluorescens strain isolated from a benzalkonium chloride solution.

    PubMed

    Nagai, K; Ohta, S; Zenda, H; Matsumoto, H; Makino, M

    1996-06-01

    A bacterium isolated as the contaminant of a batch of commercial benzalkonium chloride (BAC) solution (10% (w/v)) stored in a loosely capped bottle in the Department of Pharmacy Shinshu University Hospital was identified as Pseudomonas fluorescens belonging to biotype G of Stanier, et al. The strain was highly resistant to BAC, and the lowest concentration of BAC that inhibited visible growth of the strain as measured on nutrient agar plates was > or = 5000 micrograms/ml. BAC is a typical quaternary ammonium detergent. Thus we examined the tolerable growth concentration of various strains on surfactants. We were able to confirm growth of P. fluorescens of BAC resistance strain (PFRB) in 5% concentration, but the other strains were not able to grow in 0.1% concentration. We investigated the relationship between biotype and resistance to BAC. PFRB and three clinical isolated strains were found to be the same biotype G. However, no apparent correlation was found between the same biotypes and minimum inhibitory concentration (MIC) of disinfectant or growth permissible concentration on surfactants. The strain was unable to decompose BAC, as no growth occurred in the minimum medium containing BAC as the sole source of carbon, nitrogen or both. Our finding caused us to realize that P. fluorescens might also be a contaminant of disinfectants, as we have seen in Pseudomonas cepacia.

  5. Atmospheric pitting corrosion of 304L stainless steel: the role of highly concentrated chloride solutions.

    PubMed

    Street, Steven R; Mi, Na; Cook, Angus J M C; Mohammed-Ali, Haval B; Guo, Liya; Rayment, Trevor; Davenport, Alison J

    2015-01-01

    The morphology of atmospheric pitting corrosion in 304L stainless steel plate was analysed using MgCl(2) droplets in relation to changes in relative humidity (RH) and chloride deposition density (CDD). It was found that highly reproducible morphologies occur that are distinct at different RH. Pitting at higher concentrations, i.e. lower RH, resulted in satellite pits forming around the perimeter of wide shallow dish regions. At higher RH, these satellite pits did not form and instead spiral attack into the shallow region was observed. Increasing CDD at saturation resulted in a very broad-mouthed pitting attack within the shallow dish region. Large data sets were used to find trends in pit size and morphology in what is essentially a heterogeneous alloy. Electrochemical experiments on 304 stainless steel wires in highly saturated solutions showed that the passive current density increased significantly above 3 M MgCl(2) and the breakdown pitting potential dropped as the concentration increased. It is proposed that the shallow dish regions grow via enhanced dissolution of the passive film, whereas satellite pits and a spiral attack take place with active dissolution of bare metal surfaces.

  6. Neutron Diffraction of Aqueous Tetramethylammonium Chloride (TMA) Solutions and TMA Intercalated Swelling Clays Under Burial Conditions

    NASA Astrophysics Data System (ADS)

    Patel, R.; Howard, C. A.; Greenwell, C.; Youngs, T.; Soper, A. K.; Skipper, N. T.

    2014-12-01

    There is a need for the improvement and optimisation of clay swelling inhibitors for the enhancement of oil and gas exploration. The hydration region of both ions and the possibility of ion pairing in 1 molar aqueous solution of clay swelling inhibitor, tetramethylammonium chloride (TMACl), in D2O, under elevated hydrostatic-pressures and temperatures has been determined with unprecedented detail using a combination of neutron diffraction and small-angle scattering in conjunction with hydrogen/deuterium isotopic labeling. The O-H correlation function (H-bonds) for the water in the 1.0M solution is measured and compared with that for pure D2O. Also investigated is the effect of burial conditions on the d-spacing of TMA-intercalated vermiculite. Contrary to expectations, no aggregation of TMA ions due to hydrophobic interactions is observed, nor are any ionic pairs of TMA+ and Cl- at these burial conditions. The data revealed a more ordered water-water structure with the addition of TMACl from bulk D2O. There is no change in the hydration structure measured at the applied elevated conditions. This is in remarkable contrast to pure water at the same conditions which is well known to be compressible. The dry d-spacing of the TMA-exchanged Eucatex vermiculite is measured at 13.66 Å which increases to 14.03 Å with the addition of D2O. Beyond this, there is no change in d-spacing with increasing pressure and temperature indicating the strength of the TMA ions binding to the clay interlayers and therefore its performance as a clay-swelling inhibitor.

  7. The "kinetic capture" of an acylium ion from live aluminum chloride promoted Friedel-Crafts acylation reactions.

    PubMed

    Huang, Zhiliang; Jin, Liqun; Han, Heyou; Lei, Aiwen

    2013-03-21

    AlCl(3) promoted Friedel-Crafts acylation between 4-tert-butylbenzoyl chloride and mesitylene was investigated. The donor-acceptor complex was observed as the major species. Kinetic investigation demonstrated that the reaction was first-order on the donor-acceptor complex and zero-order on ArH, suggesting that the donor-acceptor complex was not the true reactive species. However, the acylium ion was almost invisible with a fairly low concentration under live reaction conditions. It was approved as the true reactive species through kinetic data ("kinetic capture") in the AlCl(3) promoted Friedel-Crafts acylation reaction.

  8. Solute-Derived Thermal Stabilization of Nano-sized Grains in Melt-Spun Aluminum

    NASA Astrophysics Data System (ADS)

    Baker, A. H.; Sanders, P. G.; Lass, E. A.; Kapoor, Deepak; Kampe, S. L.

    2016-08-01

    Thermal stabilization of nanograined metallic microstructures (or nanostructures) can be difficult due to the large driving force for growth that arises from the inherently significant boundary area. Kinetic approaches for stabilization of the nanostructure effective at low homologous temperatures often fail at higher homologous temperatures. Alternatively, thermodynamic approaches for thermal stabilization may offer higher temperature stability. In this research, modest alloying of aluminum with solute (1 pct by mole Sc, Yb, or Sr) was examined as a means to thermodynamically stabilize a bulk nanostructure at elevated temperatures. Following 1-hour annealing treatments at 673 K (400 °C) (0.72 Tm), 773 K (500 °C) (0.83 Tm), and 873 K (600 °C) (0.94 Tm), the alloys remain nanocrystalline (<100 nm) as measured by Warren-Averbach Fourier analysis of X-ray diffraction peaks and direct observation of TEM dark-field micrographs, with the efficacy of stabilization: Sr ≈ Yb > Sc. The disappearance of intermetallic phases in the Sr- and Yb-containing alloys in the X-ray diffraction spectra is observed to occur coincident with the stabilization after annealing, suggesting that precipitates dissolve and the boundaries are enriched with solute.

  9. Separation and preconcentration of aluminum in parenteral solutions and bottled mineral water using different analytical techniques.

    PubMed

    Kazi, Tasneem G; Khan, Sumaira; Baig, Jameel A; Kolachi, Nida F; Afridi, Hassan I; Kandhro, Ghulam A; Kumar, Sham; Shah, Abdul Q

    2009-12-30

    A new method is reported for the separation of aluminum ions [Al(III)] from interfering elements in parenteral and pharmaceutical solutions (PS) and bottled mineral water (BMW) samples, through solid-phase extraction with 2-methyl-8-hydroxyquinoline (quinaldine) adsorbed onto activated silica gel. While the enrichment step of separated Al(III) was carried out by cloud point extraction (CPE) using 8-hydroxyquinoline as complexing reagent, the resulted complex was entrapped in a non-ionic surfactant octylphenoxypolyethoxyethanol (Triton X-114). The enriched Al(III) in sample solutions were determined by spectrofluorometry (SPF) at lambda(excitation) 370 nm and lambda(emission) 510 nm, and flame atomic absorption spectrometry (FAAS) for comparative purpose. The variables affecting the complexation and extraction steps were studied and optimized. The validity of methodology was checked with certified reference material of water and standard addition method. The enrichment factor and detection limit of Al(III) for the preconcentration of 50 ml of PS and BMW were found to be 100 and 0.25 microg/L, respectively. The proposed method has been applied for the determination of trace amount of Al(III) in PS and BMW samples with satisfactory results. In PS the levels of Al(III) are above than permissible limit (25 microg/L).

  10. Ultrasonic Spray-Assisted Solution-Based Vapor-Deposition of Aluminum Tris(8-hydroxyquinoline) Thin Films

    NASA Astrophysics Data System (ADS)

    Piao, Jinchun; Katori, Shigetaka; Ikenoue, Takumi; Fujita, Shizuo

    2011-02-01

    Aluminum tris(8-hydroxyquinoline) (Alq3) thin films were fabricated by a vapor-deposition technique from its methanol solution, that is, by the ultrasonic-assisted mist deposition technique. The application of high ultrasonic power to the Alq3-methanol mixture resulted in a stable and transparent solution. Mist particles formed by ultrasonic atomization of the solution were used as the source for vapor-deposition at the substrate temperature of 100-200 °C. Optical absorption and photoluminescence characteristics indicated the formation of Alq3 thin films. The results promise the formation of thin films of a variety of organic materials by the solution-based technique.

  11. Dual blockade of the A1 and A2A adenosine receptor prevents amyloid beta toxicity in neuroblastoma cells exposed to aluminum chloride.

    PubMed

    Giunta, Salvatore; Andriolo, Violetta; Castorina, Alessandro

    2014-09-01

    In a previous work we have shown that exposure to aluminum (Al) chloride (AlCl3) enhanced the neurotoxicity of the amyloid beta(25-35) fragment (Abeta(25-35)) in neuroblastoma cells and affected the expression of Alzheimer's disease (AD)-related genes. Caffein, a compound endowed with beneficial effects against AD, exerts neuroprotection primarily through its antagonist activity on A2A adenosine receptors (A2AR), although it also inhibits A1Rs with similar potency. Still, studies on the specific involvement of these receptors in neuroprotection in a model of combined neurotoxicity (Abeta(25-35)+AlCl3) are missing. To address this issue, cultured SH-SY5Y cells exposed to Abeta(25-35)+AlCl3 were assessed for cell viability, morphology, intracellular ROS activity and expression of apoptosis-, stress- and AD-related proteins. To define the role of A1R and A2ARs, pretreatment with caffein, specific receptor antagonists (DPCPX or SCH58261) or siRNA-mediated gene knockdown were delivered. Results indicate that AlCl3 treatment exacerbated Abeta(25-35) toxicity, increased ROS production, lipid peroxidation, β-secretase-1 (BACE1) and amyloid precursor protein (APP). Interestingly, SCH58261 successfully prevented toxicity associated to Abeta(25-35) only, whereas pretreatment with both DPCPX and SCH58261 was required to fully avert Abeta(25-35)+AlCl3-induced damage, suggesting that A1Rs might also be critically involved in protection during combined toxicity. The effects of caffein were mimicked by both N-acetyl cysteine, an antioxidant, and desferrioxamine, likely acting through distinct mechanisms. Altogether, our data establish a novel protective function associated with A1R inhibition in the setting of combined Abeta(25-35)+AlCl3 neurotoxicity, and expand our current knowledge on the potential beneficial role of caffein to prevent AD progression in subjects environmentally exposed to aluminum.

  12. A spectrophotometric study of neodymium(III) complexation in chloride solutions

    NASA Astrophysics Data System (ADS)

    Migdisov, Art A.; Williams-Jones, A. E.

    2002-12-01

    The formation constants of neodymium complexes in chloride solutions have been determined spectrophotometrically at temperatures of 25 to 250°C and a pressure of 50 bars. The simple ion, Nd 3+, is dominant at 25°C, whereas NdCl 2+ and NdCl 2+ are the dominant species at elevated temperatures. Equilibrium constants were calculated for the following reactions: Nd 3+ + Cl - = NdCl 2+ β 1, Nd 3+ + 2 · Cl - = NdCl +2 β 2. The values of β 1 were found to be identical within experimental error to the values reported by Gammons et al. (1996) but substantially different from those proposed by Stepanchikova and Kolonin (1999). The values of β 2 obtained in this study agree relatively well with those of Gammons et al. (1996); differences are greatest at intermediate temperature and reach a maximum of one half an order of magnitude at 200°C. Theoretical estimates of β 1 and β 2 by Haas et al. (1995) using the revised Helgeson-Kirkham-Flowers (HKF) equation of state predict lower stability of NdCl 2+ and NdCl 2+ at temperatures above 150°C than determined in this study. A new fit to the HKF equation of state is therefore proposed, which yields values for β 1 and β 2 similar to those obtained experimentally. Using the formation constants reported in this study, we predict that typical seafloor hydrothermal vent fluids will contain a maximum concentration of Nd of ˜2 ppb. This value is several orders of magnitude lower than would be required to explain the levels of Nd mobility commonly reported for seafloor hydrothermal systems and suggests that other ligands may be more important than Cl in transporting rare earth elements in the Earth's crust.

  13. Aqueous Solutions of the Ionic Liquid 1-butyl-3-methylimidazolium Chloride Denature Proteins

    SciTech Connect

    Baker, Gary A; Heller, William T

    2009-01-01

    As we advance our understanding, ionic liquids (ILs) are finding ever broader scope within the chemical sciences including, most recently, pharmaceutical, enzymatic, and bioanalytical applications. With examples of enzymatic activity reported in both neat ILs and in IL/water mixtures, enzymes are frequently assumed to adopt a quasi-native conformation, even if little work has been carried out to date toward characterizing the conformation, dynamics, active-site perturbation, cooperativity of unfolding transitions, free energy of stabilization, or aggregation/oligomerization state of enzymes in the presence of an IL solvent component. In this study, human serum albumin and equine heart cytochrome c were characterized in aqueous solutions of the fully water-miscible IL 1-butyl-3-methylimidazolium chloride, [bmim]Cl, by small-angle neutron and X-ray scattering. At [bmim]Cl concentrations up to 25 vol.%, these two proteins were found to largely retain their higher-order structures whereas both proteins become highly denatured at the highest IL concentration studied here (i.e., 50 vol.% [bmim]Cl). The response of these proteins to [bmim]Cl is analogous to their behavior in the widely studied denaturants guanidine hydrochloride and urea which similarly lead to random coil conformations at excessive molar concentrations. Interestingly, human serum albumin dimerizes in response to [bmim]Cl, whereas cytochrome c remains predominantly in monomeric form. These results have important implications for enzymatic studies in aqueous IL media, as they suggest a facile pathway through which biocatalytic activity can be altered in these nascent and potentially green electrolyte systems.

  14. Effect of Organic Acid Additions on the General and Localized Corrosion Susceptibility of Alloy 22 in Chloride Solutions

    SciTech Connect

    Carranza, R M; Giordano, C M; Rodr?guez, M A; Ilevbare, G O; Rebak, R B

    2007-08-28

    Electrochemical studies such as cyclic potentiodynamic polarization (CPP) and electrochemical impedance spectroscopy (EIS) were performed to determine the corrosion behavior of Alloy 22 (N06022) in 1M NaCl solutions at various pH values from acidic to neutral at 90 C. All the tested material was wrought Mill Annealed (MA). Tests were also performed in NaCl solutions containing weak organic acids such as oxalic, acetic, citric and picric. Results show that the corrosion rate of Alloy 22 was significantly higher in solutions containing oxalic acid than in solutions of pure NaCl at the same pH. Citric and picric acids showed a slightly higher corrosion rate, and acetic acid maintained the corrosion rate of pure chloride solutions at the same pH. Organic acids revealed to be weak inhibitors for crevice corrosion. Higher concentration ratios, compared to nitrate ions, were needed to completely inhibit crevice corrosion in chloride solutions. Results are discussed considering acid dissociation constants, buffer capacity and complex formation constants of the different weak acids.

  15. Influence on the generation of disinfection byproducts in a tannic acid solution by aluminum ions.

    PubMed

    Shen, Hong; Chen, Xin; Chen, Hongbin

    2016-08-17

    Aluminum (Al) commonly exists in natural waters, and its salts are often used as coagulants in drinking water treatment. Therefore, associated with the security of drinking water, functions of Al ions (Al(3+)) on generation of disinfection byproducts (DBPs) should not be ignored. This study focuses on DBPs and the carcinogenic factor of chlorinated water samples after the addition of Al(3+) with different Al(3+)/initial tannic acid molar ratios. The results imply that Al(3+) acts as a promoter of haloacetic acids (HAAs) and an inhibitor of trihalomethanes (THMs) when tannic acid is selected as model compound of natural organic matter during chlorination. Depending on the results of size exclusion chromatography and ultraviolet spectrophotometer, an equilibrium system can be assumed between hydrolysis and flocculation in tannic acid solution with Al(3+). Furthermore, influences on the equilibrium system for Al(3+) addition may result in various effects on generation and distribution ratios of THMs and HAAs during chlorination. Finally, according to the analyses of a fluorescence spectrophotometer, it is demonstrated that the presence of Al(3+) helps to increase precursors of DBPs (humic acid-like organics) and then improve the generation of DBPs.

  16. A solution NMR investigation into the early events of amelogenin nanosphere self-assembly initiated with sodium chloride or calcium chloride.

    PubMed

    Buchko, Garry W; Tarasevich, Barbara J; Bekhazi, Jacky; Snead, Malcolm L; Shaw, Wendy J

    2008-12-16

    Using solution-state NMR spectroscopy, new insights into the early events governing amelogenin supramolecular self-assembly have been identified using sodium chloride and calcium chloride to trigger the association. Two-dimensional 1H-15N HSQC spectra were recorded for 15N- and 13C-labeled murine amelogenin as a function of increasing NaCl and CaCl2 concentration beginning with solution conditions of 2% acetic acid at pH 3.0, where amelogenin was monomeric. Residue specific changes in molecular dynamics, manifested by the reduction in intensity and disappearance of 1H-15N HSQC cross-peaks, were observed with the addition of either salt to the protein. With increasing NaCl concentrations, residues between T21 and R31 near the N-terminus were affected first, suggesting that these residues may initiate amelogenin dimerization, the first step in nanosphere assembly. At higher NaCl concentrations, more residues near the N-terminus (Y12-I51) were affected, and with further additions of NaCl, residues near the C-terminus (L141-T171) began to show a similar change in molecular dynamics. With increasing CaCl2 concentrations, a similar stepwise change in molecular dynamics involving essentially the same set of amelogenin residues was observed. As the concentration of either salt was increased, a concomitant increase in the estimated overall rotational correlation time (tau(c)) was observed, consistent with assembly. Self-assembly into a dimer or trimer was established with dynamic light scattering studies under similar conditions that showed an increase in diameter of the smallest species from 4.1 nm in the absence of salt to 10 nm in the presence of salt. These results suggest a possible stepwise interaction mechanism, starting with the N-terminus and followed by the C-terminus, leading to amelogenin nanosphere assembly.

  17. Effects of poly aluminum chloride dosing positions on the performance of a pilot scale anoxic/oxic-membrane bioreactor (A/O-MBR).

    PubMed

    Guo, Shaodong; Qu, Fangshu; Ding, An; Bai, Langming; Li, Guibai; Ngo, Huu Hao; Guo, Wenshan; Liang, Heng

    2015-01-01

    The effects of poly aluminum chloride (PACl) dosing positions on the performance of a pilot scale anoxic/oxic membrane bioreactor were investigated. PACl dosage was optimized at 19.5 mg Al2O3/L by jar test. Nutrients removal efficiencies and sludge properties were systematically investigated during periods with no PACl dosing (phase I), with PACl dosing in oxic tank (phase II) and then in anoxic tank (phase III). The results showed that total phosphorus removal efficiency increased from 18 to 88% in phase II and 85% in phase III with less than 0.5 mg P/L in effluent. Ammonia nitrogen removal efficiencies reached 99% in all phases and chemical oxygen demand removal efficiencies reached 92%, 91% and 90% in the three phases, respectively. Total nitrogen removal efficiency decreased from 59% in phase I to 49% in phases II and III. Dosing PACl in the oxic tank resulted in smaller sludge particle size, higher zeta potential, better sludge settleability and lower membrane fouling rate in comparison with dosing PACl in the anoxic tank.

  18. Efficiency of aluminum-pillared montmorillonite on the removal of cesium and copper from aqueous solutions.

    PubMed

    Karamanis, D; Assimakopoulos, P A

    2007-05-01

    Aluminum-pillared-layered montmorillonites (PILMs) were tested for their potential application in the removal of copper or cesium from aqueous solutions. By varying the initial conditions, several PILMs were prepared and characterized by means of X-ray fluorescence (XRF), proton induced gamma-ray emission (PIGE), X-ray diffraction (XRD) and sorption isotherms. Uptake of metals was studied by means of XRF spectrometry for copper sorption or gamma-ray spectrometry for cesium, using 137Cs as radiotracer. The sorption kinetics and capacity of PILMs were determined in relation to the effects of factors such as the initial metal concentration, initial pH of the solution and the presence of competitive cations. Kinetic studies showed that an equilibrium time of few minutes was needed for the adsorption of metal ions on PILMs. A pseudo-first-order equation was used to describe the sorption process for either copper or cesium. The most effective pH range for the removal of copper and cesium was found to be 4.0-6.0 and 3.0-8.0, respectively. Cesium sorption isotherms were best represented by a two-site Langmuir model while copper isotherms followed the Freundlich or the two-site Langmuir model. Cesium sorption experiments with inorganic or organic competitive cations as blocking agents revealed that the high selective sites of PILMs for cesium sorption (1-2% of total) are surface and edge sites in addition to interlayer exchange sites. In copper sorption, the two sites were determined as interlayer sites of PILMs after restoring their cation exchange capacity and sites associated with the pillar oxides.

  19. Aluminum Chloride Induces Osteoblasts Apoptosis via Disrupting Calcium Homeostasis and Activating Ca(2+)/CaMKII Signal Pathway.

    PubMed

    Cao, Zheng; Liu, Dawei; Zhang, Qiuyue; Sun, Xudong; Li, Yanfei

    2016-02-01

    Aluminum promotes osteoblast (OB) apoptosis. Apoptosis is induced by the disordered calcium homeostasis. Therefore, to investigate the relationship between Al-induced OB apoptosis and calcium homeostasis, calvarium OBs from neonatal rats (3-4 days) were cultured and exposed to 0.048-mg/mL Al(3+) or 0.048-mg/mL Al(3+) combined with 5 μM BAPTA-AM (OBs were pretreated with 5 μM BAPTA-AM for 1 h, then added 0.048 mg/mL Al(3+)), respectively. Then OB apoptosis rate, intracellular calcium ions concentration ([Ca(2+)]i), mRNA expression level of calmodulin (CaM), and protein expression levels of CaM and p-CaMKII in OBs were examined. The result showed that AlCl3 increased OB apoptosis rate, and [Ca(2+)]i and p-CaMKII expression levels and decreased CaM expression levels, whereas BAPTA-AM relieved the effects. These results proved that AlCl3 induced OB apoptosis by disrupting the intracellular Ca(2+) homeostasis and activating the Ca(2+)/CaMKII signal pathway. Our findings can provide new insights for revealing the apoptosis mechanism of OBs exposed to AlCl3.

  20. Direct conversion of cellulose to 1-(furan-2-yl)-2-hydroxyethanone in zinc chloride solution under microwave irradiation.

    PubMed

    Yang, Lei; Li, Gang; Yang, Fang; Zhang, Song-Mei; Fan, Hong-Xian; Lv, Xiao-Na

    2011-10-18

    Conversion of cellulose to 1-(furan-2-yl)-2-hydroxyethanone has been demonstrated in concentrated zinc chloride solution under microwave irradiation. Compared with the conventional oil-bath heating mode, microwave irradiation significantly reduced the reaction time and increased the yield of 1-(furan-2-yl)-2-hydroxyethanone. A typical degradation reaction with cellulose produced 1-(furan-2-yl)-2-hydroxyethanone in 12.0% molar yield in ZnCl(2) solution (ZnCl(2)-H(2)O ratio=2.25:1, w/w) with microwave irradiation at 600 W for 5 minutes at 135°C.

  1. Chemical model for the solvent extraction of GdCl3 from a chloride solution with saponified PC88A

    NASA Astrophysics Data System (ADS)

    Lee, Man-Seung; Lee, Jin-Young; Kim, Joon-Soo

    2005-12-01

    Solvent extraction experiments of Gd with 40% saponified PC88A have been conducted from a chloride solution under different extraction conditions. The effect of saponification of an acidic extractant on the extraction of Gd was investigated. To analyze the ionic equilibria of a GdCl3 solution, we estimated the necessary thermodynamic properties from reported values. Moreover, when applying the chemical model developed in this study, we used experimental data to estimate the equilibrium constant for the extraction of Gd with partially saponified PC88A.

  2. Investigation of the aluminum phthalocyanine nanoparticles colloidal solutions pH-dependent photoluminescence kinetics in pico- and nanosecond time range

    NASA Astrophysics Data System (ADS)

    Bystrov, F. G.; Makarov, V. I.; Loschenov, V. B.

    2016-08-01

    In this study, the fluorescence intensity decay of aluminum phthalocyanine nanoparticles colloidal solutions at different pH was investigated. Hamamatsu Streak-Camera (C10627 - 13 Hamamatsu Photonics) with picosecond temporal resolution (15 ps) was used to carry out the measurements. For excitation we used Hamamatsu Picosecond Light Pulser PLP - 10 with 637 nm wavelength and 65 ps pulse duration. The changes in fluorescence decay kinetics were found during the experiment. The number of fluorescence lifetime components and duration of lifetimes depends on pH. At pH 2 the presence of two fluorescence lifetimes was recorded: the first one was 5 ns, which corresponded to the molecular form in solution, and 1.5 ns, which corresponded to bound state of phthalocyanine molecules. This work is a preparatory step towards a model which describes the interaction of aluminum phthalocyanine nanoparticles with environment in biological tissue.

  3. [Removal of nitrate from aqueous solution using cetylpyridinium chloride (CPC)-modified activated carbon as the adsorbent].

    PubMed

    Zheng, Wen-Jing; Lin, Jian-Wei; Zhan, Yan-Hui; Fang, Qiao; Yang, Meng-Juan; Wang, Hong

    2013-11-01

    Surfactant-modified activated carbon (SMAC) was prepared by loading cetylpyridinium chloride (CPC) onto activated carbon and used as adsorbents to remove nitrate from aqueous solution. The SMAC was effective for removing nitrate from aqueous solution. The SMAC exhibited much higher nitrate adsorption capacity than that of the unmodified activated carbon. The nitrate adsorption capacity for SMAC increased with increasing the CPC loading. The adsorption kinetics of nitrate on SMAC followed a pseudo-second-order kinetic model. The equilibrium adsorption data of nitrate on SMAC could be described by the Langmuir isotherm model. Based on the Langmuir isotherm model, the maximum nitrate adsorption capacity for SMAC with CPC loading amount of444 mmol per 1 kg activated carbon was determined to be 16.1 mg x g(-1). The nitrate adsorption capacity for SMAC decreased with the increasing solution pH. The presence of competing anions such as chloride, sulfate and bicarbonate reduced the nitrate adsorption capacity. The nitrate adsorption capacity for SMAC slightly decreased with the increasing reaction temperature. Almost 95% of nitrate molecules adsorbed on SMAC could be desorbed in 1 mol x L(-1) NaCl solution. The main mechanisms for the adsorption of nitrate on SMAC are anionic exchange and electrostatic attraction. The results of this work indicate that SMAC is a promising adsorbent for removing nitrate from aqueous solution.

  4. Virus inactivation in aluminum and polyaluminum coagulation.

    PubMed

    Matsui, Yoshihiko; Matsushita, Taku; Sakuma, Satoru; Gojo, Takahito; Mamiya, Teppei; Suzuoki, Hiroshi; Inoue, Takanobu

    2003-11-15

    Inorganic aluminum salts, such as aluminum sulfate, are coagulants that cause small particles, such as bacteria and viruses as well as inorganic particles, to destabilize and combine into larger aggregates. In this investigation, batch coagulation treatments of water samples spiked with Qbeta, MS2, T4, and P1 viruses were conducted with four different aluminum coagulants. The total infectious virus concentration in the suspension of floc particles that eventually formed by dosing with coagulant was measured after the floc particles were dissolved by raising the pH with an alkaline beef extract solution. The virus concentrations were extremely reduced after the water samples were dosed with aluminum coagulants. Viruses mixed with and adsorbed onto preformed aluminum hydroxide floc were, however, completely recovered after the floc dissolution. These results indicated that the aluminum coagulation process inactivates viruses. Virucidal activity was most prominent with the prehydrolyzed aluminum salt coagulant, polyaluminum chloride (PACl). Virucidal activity was lower in river water than in ultrapure water--natural organic matter in the river water depressed the virucidal activity. Mechanisms and kinetics of the virus inactivation were discussed. Our results suggest that intermediate polymers formed during hydrolysis of the aluminum coagulants sorbed strongly to viruses, either rendering them inactive or preventing infectivity.

  5. Effect of benzalkonium chloride-free latanoprost ophthalmic solution on ocular surface in patients with glaucoma

    PubMed Central

    Walimbe, Tejaswini; Chelerkar, Vidya; Bhagat, Purvi; Joshi, Abhijeet; Raut, Atul

    2016-01-01

    Introduction Benzalkonium chloride (BAK), included as a preservative in many topical treatments for glaucoma, induces significant toxicity and alters tear breakup time (TBUT). BAK-containing latanoprost, an ester prodrug of prostaglandin F2α, can cause ocular adverse events (AEs) associated with BAK. The purpose of this study was to evaluate the efficacy and safety of BAK-free latanoprost. Patients and methods A prospective, open-label, single-arm, multicenter, 8-week study in patients with primary open-angle glaucoma or ocular hypertension taking BAK-containing latanoprost for ≥12 months was performed. Patients were switched to BAK-free latanoprost ophthalmic solution 0.005% administered once daily, and eyes were assessed after 28 and 56 days. Primary efficacy and safety variables were TBUT and treatment-emergent AEs, respectively. Results At day 56, 40 eyes were evaluable. Mean TBUT increased significantly from baseline (3.67±1.60 seconds) to 5.03±2.64 and 6.06±3.39 seconds after 28 and 56 days of treatment with BAK-free latanoprost (P<0.0001). Ocular Surface Disease Index© (OSDI©) score also decreased significantly to 12.06±13.40 and 7.06±10.75 at 28 and 56 days, respectively, versus baseline (18.09±18.61, P<0.0001). In addition, inferior corneal staining score decreased significantly to 0.53 from baseline (0.85, P=0.0033). A reduction in conjunctival hyperemia and intraocular pressure was observed at both time points. No treatment-related serious AEs were evident and 12 (26.08%) treatment-emergent AEs occurred in seven patients, with eye pain and irritation being the most frequent. No clinically significant changes in vital signs or slit lamp examinations were observed. Conclusion Results indicate that switching from BAK-containing latanoprost to BAK-free latanoprost resulted in significant improvements in TBUT, OSDI© score, and inferior corneal staining score, and measurable reductions in conjunctival hyperemia score. Furthermore, BAK

  6. Lead, cadmium and aluminum in Canadian infant formulae, oral electrolytes and glucose solutions.

    PubMed

    Dabeka, Robert; Fouquet, Andre; Belisle, Stephane; Turcotte, Stephane

    2011-06-01

    Lead (Pb), cadmium (Cd) and aluminum (Al) were determined in 437 individual samples of infant formulae, oral electrolytes and 5% glucose solutions available in Canada. In the electrolytes, Cd and Pb concentrations were all below 0.01 and 0.041 ng g(-1), respectively. In the 5% glucose solutions, Pb and Cd levels averaged 0.01 and 0.09 ng g(-1), respectively. Reported on an as-consumed basis, Pb levels in milk- and soya-based formulae averaged 0.90 and 1.45 ng g(-1), respectively, while Cd levels averaged 0.23 and 1.18 ng g(-1), respectively Average Al levels on an as-consumed basis were 440 ng g(-1) (range 10-3400 ng g(-1)) in milk-based formulae and 730 ng g(-1) (range 230-1100 ng g(-1)) in soy-based formulae. Al concentrations increased in the following order: plain formula < low-iron formula < iron-supplemented formula < casein hydrolysate formula ≈ premature formula ≤ soy formula. For example, in the powdered formulae, average Al concentrations were 18 ng g(-1) for plain milk-based, 37 ng g(-1) for low-iron, 128 ng g(-1) for iron supplemented, 462 ng g(-1) for lactose-free, 518 ng g(-1) for hypoallergenic and 619 ng g(-1) for soy-based formula. Al concentrations, as-consumed, increased with decreasing levels of concentration: powder < concentrated liquid < ready-to-use. Formulae stored in glass bottles contained between 100 and 300 ng g(-1) more Al than the same formulae stored in cans. The source of the increased Al did not appear to be the glass itself, because most electrolytes and glucose solutions, also stored in glass, contained less than 8 ng g(-1) Al. Corresponding differences in Pb and Cd levels were not observed. Al concentrations varied substantially among manufacturers; however, all manufacturers were able to produce plain milk-based formulae containing less than 50 ng g(-1) Al, i.e. within the range of Al concentrations found in human milk. Next to soya-based and hypoallergenic formulae, premature formulae contained among the highest

  7. Lead, cadmium and aluminum in Canadian infant formulae, oral electrolytes and glucose solutions

    PubMed Central

    Dabeka, Robert; Fouquet, Andre; Belisle, Stephane; Turcotte, Stephane

    2011-01-01

    Lead (Pb), cadmium (Cd) and aluminum (Al) were determined in 437 individual samples of infant formulae, oral electrolytes and 5% glucose solutions available in Canada. In the electrolytes, Cd and Pb concentrations were all below 0.01 and 0.041 ng g−1, respectively. In the 5% glucose solutions, Pb and Cd levels averaged 0.01 and 0.09 ng g−1, respectively. Reported on an as-consumed basis, Pb levels in milk- and soya-based formulae averaged 0.90 and 1.45 ng g−1, respectively, while Cd levels averaged 0.23 and 1.18 ng g−1, respectively Average Al levels on an as-consumed basis were 440 ng g−1 (range 10–3400 ng g−1) in milk-based formulae and 730 ng g−1 (range 230–1100 ng g−1) in soy-based formulae. Al concentrations increased in the following order: plain formula < low-iron formula < iron-supplemented formula < casein hydrolysate formula ≈ premature formula ≤ soy formula. For example, in the powdered formulae, average Al concentrations were 18 ng g−1 for plain milk-based, 37 ng g−1 for low-iron, 128 ng g−1 for iron supplemented, 462 ng g−1 for lactose-free, 518 ng g−1 for hypoallergenic and 619 ng g−1 for soy-based formula. Al concentrations, as-consumed, increased with decreasing levels of concentration: powder < concentrated liquid < ready-to-use. Formulae stored in glass bottles contained between 100 and 300 ng g−1 more Al than the same formulae stored in cans. The source of the increased Al did not appear to be the glass itself, because most electrolytes and glucose solutions, also stored in glass, contained less than 8 ng g−1 Al. Corresponding differences in Pb and Cd levels were not observed. Al concentrations varied substantially among manufacturers; however, all manufacturers were able to produce plain milk-based formulae containing less than 50 ng g−1 Al, i.e. within the range of Al concentrations found in human milk. Next to soya-based and hypoallergenic formulae, premature formulae contained among the highest

  8. Analysis of the corrosion of carbon steels in simulated salt repository brines and acid chloride solutions at high temperatures

    SciTech Connect

    Diercks, D.R.; Kassner, T.F.

    1988-04-01

    An analysis of literature data on the corrosion of carbon steels in anoxic brines and acid chloride solutions was performed, and the results were used to assess the expected life of high-level nuclear waste package containers in a salt repository environment. The corrosion rate of carbon steels in moderately acidic aqueous chloride environments obeys an Arrhenius dependence on temperature and a (pH{sub 2}){sup {minus}1/2} dependence on hydrogen partial pressure. The cathodic reduction of water to produce hydrogen is the rate-controlling step in the corrosion process. An expression for the corrosion rate incorporating these two dependencies was used to estimate the corrosion life of several proposed waste package configurations. 42 refs., 11 figs., 2 tabs.

  9. Antimicrobial effects of electrolytic products of sodium chloride--comparative evaluation with sodium hypochlorite solution and efficacy in handwashing.

    PubMed

    Hitomi, S; Baba, S; Yano, H; Morisawa, Y; Kimura, S

    1998-11-01

    We examined the in vitro bactericidal effects and efficacy on handwashing of water containing electrolytic products of sodium chloride (electrolytic water). The electrolytic water, whose pH and concentration of free residual chlorine were 6.7-6.9 and 20-22 ppm, respectively, showed equal reduction of both Staphylococcus aureus and Escherichia coli to dilution of commercially available sodium hypochlorite containing 60 ppm of free residual chlorine. This bactericidal effect was calculated to be due to hypochlorous acid, based on the pH and the amount of chlorine in solution. Handwashing with the electrolytic water reduced the numbers of S. aureus on hands by 1/10(2), while running water and 0.2% benzalkonium chloride with 80% ethanol gave a 1/10 and 1/10(5) reduction, respectively. We conclude that electrolytic water might be applicable for handwashing in place of running water.

  10. Effects of temperature and pressure on stress corrosion cracking behavior of 310S stainless steel in chloride solution

    NASA Astrophysics Data System (ADS)

    Zhong, Yunpan; Zhou, Cheng; Chen, Songying; Wang, Ruiyan

    2017-01-01

    310S is an austenitic stainless steel for high temperature applications, having strong resistance of oxidation, hydrogen embrittlement and corrosion. Stress corrosion cracking(SCC) is the main corrosion failure mode for 310S stainless steel. Past researched about SCC of 310S primarily focus on the corrosion mechanism and influence of temperature and corrosive media, but few studies concern the combined influence of temperature, pressure and chloride. For a better understanding of temperature and pressure's effects on SCC of 310S stainless steel, prepared samples are investigated via slow strain rate tensile test(SSRT) in different temperature and pressure in NACE A solution. The result shows that the SCC sensibility indexes of 310S stainless steel increase with the rise of temperature and reach maximum at 10MPa and 160°C, increasing by 22.3% compared with that at 10 MPa and 80 °C. Instead, the sensibility decreases with the pressure up. Besides, the fractures begin to transform from the ductile fracture to the brittle fracture with the increase of temperature. 310S stainless steel has an obvious tendency of stress corrosion at 10MPa and 160°C and the fracture surface exists cleavage steps, river patterns and some local secondary cracks, having obvious brittle fracture characteristics. The SCC cracks initiate from inclusions and tiny pits in the matrix and propagate into the matrix along the cross section gradually until rupture. In particular, the oxygen and chloride play an important role on the SCC of 310S stainless steel in NACE A solution. The chloride damages passivating film, causing pitting corrosion, concentrating in the cracks and accelerated SSC ultimately. The research reveals the combined influence of temperature, pressure and chloride on the SCC of 310S, which can be a guide to the application of 310S stainless steel in super-heater tube.

  11. Corrosion behavior of austenitic stainless steels in chloride containing ozone solutions

    SciTech Connect

    Pohjanne, P.

    1997-08-01

    Environmental concern about chlorinated organic compounds generated from traditional bleach plants has led to a development of new environmentally friendly bleaching processes. Recently, the development of ozone bleaching has progressed from pilot operations to production scale installations. Ozone is currently used as a bleaching agent of pulp as a replacement for chlorine based bleaching chemicals. Yet, there are few articles which are dealing with ozone and its effect to corrosion resistance of stainless steels or any other construction materials used in bleaching equipment. In this paper corrosion behavior of austenitic stainless steels, grades AISI 316, AISI 317LNM, UNS S31254 and UNS 32654 PM, were studied in simulated ozone bleaching environments. The laboratory tests showed that in ozone environments without chlorides the corrosion resistance of AISI 316 was superior to that of the high-alloyed stainless steels, due to the relatively low amount of alloying elements. The sequence was reversed in ozone environments containing chlorides. In the presence of chlorides AISI 316 was susceptible to localized corrosion whereas the high-alloyed UNS S31254 and UNS S 32654 PM were resistant to localized corrosion in all chloride concentrations examined.

  12. 46 CFR 151.50-34 - Vinyl chloride (vinyl chloride monomer).

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 46 Shipping 5 2011-10-01 2011-10-01 false Vinyl chloride (vinyl chloride monomer). 151.50-34... chloride (vinyl chloride monomer). (a) Copper, aluminum, magnesium, mercury, silver, and their alloys shall... equipment that may come in contact with vinyl chloride liquid or vapor. (b) Valves, flanges, and...

  13. 46 CFR 151.50-34 - Vinyl chloride (vinyl chloride monomer).

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 46 Shipping 5 2013-10-01 2013-10-01 false Vinyl chloride (vinyl chloride monomer). 151.50-34... chloride (vinyl chloride monomer). (a) Copper, aluminum, magnesium, mercury, silver, and their alloys shall... equipment that may come in contact with vinyl chloride liquid or vapor. (b) Valves, flanges, and...

  14. 46 CFR 151.50-34 - Vinyl chloride (vinyl chloride monomer).

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 46 Shipping 5 2014-10-01 2014-10-01 false Vinyl chloride (vinyl chloride monomer). 151.50-34... chloride (vinyl chloride monomer). (a) Copper, aluminum, magnesium, mercury, silver, and their alloys shall... equipment that may come in contact with vinyl chloride liquid or vapor. (b) Valves, flanges, and...

  15. Selective conversion of cellulose in corncob residue to levulinic acid in an aluminum trichloride-sodium chloride system.

    PubMed

    Li, Jianmei; Jiang, Zhicheng; Hu, Libin; Hu, Changwei

    2014-09-01

    Increased energy consumption and environmental concerns have driven efforts to produce chemicals from renewable biomass with high selectivity. Here, the selective conversion of cellulose in corncob residue, a process waste from the production of xylose, to levulinic acid was carried out using AlCl3 as catalyst and NaCl as promoter by a hydrothermal method at relatively low temperature. A levulinic acid yield of 46.8 mol% was obtained, and the total selectivity to levulinic acid with formic acid was beyond 90%. NaCl selectively promoted the dissolution of cellulose from corncob residue, and significantly improved the yield and selectivity to levulinic acid by inhibiting lactic acid formation in the subsequent dehydration process. Owing to the salt effect of NaCl, the obtained levulinic acid could be efficiently extracted to tetrahydrofuran from aqueous solution. The aqueous solution with AlCl3 and NaCl could be recycled 4 times. Because of the limited conversion of lignin, this process allows for the production of levulinic acid with high selectivity directly from corncob residue in a simple separation process.

  16. Infrared optical constants of crystalline sodium chloride dihydrate: application to study the crystallization of aqueous sodium chloride solution droplets at low temperatures.

    PubMed

    Wagner, Robert; Möhler, Ottmar; Schnaiter, Martin

    2012-08-23

    Complex refractive indices of sodium chloride dihydrate, NaCl·2H(2)O, have been retrieved in the 6000-800 cm(-1) wavenumber regime from the infrared extinction spectra of crystallized aqueous NaCl solution droplets. The data set is valid in the temperature range from 235 to 216 K and was inferred from crystallization experiments with airborne particles performed in the large coolable aerosol and cloud chamber AIDA at the Karlsruhe Institute of Technology. The retrieval concept was based on the Kramers-Kronig relationship for a complex function of the optical constants n and k whose imaginary part is proportional to the optical depth of a small particle absorption spectrum in the Rayleigh approximation. The appropriate proportionality factor was inferred from a fitting algorithm applied to the extinction spectra of about 1 μm sized particles, which, apart from absorption, also featured a pronounced scattering contribution. NaCl·2H(2)O is the thermodynamically stable crystalline solid in the sodium chloride-water system below the peritectic at 273.3 K; above 273.3 K, the anhydrous NaCl is more stable. In contrast to anhydrous NaCl crystals, the dihydrate particles reveal prominent absorption signatures at mid-infrared wavelengths due to the hydration water molecules. Formation of NaCl·2H(2)O was only detected at temperatures clearly below the peritectic and was first evidenced in a crystallization experiment conducted at 235 K. We have employed the retrieved refractive indices of NaCl·2H(2)O to quantify the temperature dependent partitioning between anhydrous and dihydrate NaCl particles upon crystallization of aqueous NaCl solution droplets. It was found that the temperature range from 235 to 216 K represents the transition regime where the composition of the crystallized particle ensemble changes from almost only NaCl to almost only NaCl·2H(2)O particles. Compared to the findings on the NaCl/NaCl·2H(2)O partitioning from a recent study conducted with micron

  17. Development of a Combined Solution Formulation of Atropine Sulfate and Obidoxime Chloride for Autoinjector and Evaluation of Its Stability

    PubMed Central

    Ettehadi, Hossein Ali; Ghalandari, Rouhollah; Shafaati, Alireza; Foroutan, Seyed Mohsen

    2013-01-01

    Atropine (AT) and oximes, alone or in combination, have been proven greatly valuable therapeutics in the treatment of organophosphates intoxications. An injectable mixture of AT and obidoxime (OB) was formulated for the administration by automatic self-injector. The aqueous single dose solution contained 275 mg obidoxime chloride and 2.5 mg atropine sulfate per 1 mL (220 mg and 2 mg per 0.8 effective dose, respectively). The final solution was sterilized by filtration through a 0.22 μm pore size filter. This more concentrated solution allowed to use a smaller size and lighter weight cartridge. Quality control tests, including assay of the two major compounds were performed separately, using reversed-phase HPLC methods. Besides, the stability test was carried out according to ICH guideline for the accelerated test. The obtained results showed that the proposed formulation is stable over a period of 2 years after preparation. PMID:24250669

  18. Structural, dynamic, and transport properties of concentrated aqueous sodium chloride solutions under an external static electric field.

    PubMed

    Ren, Gan; Shi, Rui; Wang, Yanting

    2014-04-24

    In the absence of an external electric field, it has already been known that ion clusters are formed instantaneously in moderately concentrated ionic solutions. In this work, we use molecular dynamics (MD) simulations to investigate the changes of structural, dynamic, and transport properties in a sodium chloride solution under an external electric field from the ion cluster perspective. Our MD simulation results indicate that, with a strong external electric field E (≥0.1 V/nm) applied, ion clusters become smaller and less net charged, and the structures and dynamics as well as transport properties of the ion solution become anisotropic. The influence of the cluster structure and shell structure to transport properties was analyzed and the Einstein relation was found invalid in this system.

  19. Effect of Polyvnylpyrrolidone (PVP) in Binary Solution on the Performance of Polyethersulfone Hollow Fibre Membrane for Sodium Chloride Separation

    NASA Astrophysics Data System (ADS)

    Bolong, N.; Ismail, A. F.; Salim, M. R.

    2010-03-01

    In membrane preparation, phase inversion is a versatile technique that allow polymer to be transformed from liquid to a solid state in a controlled manner. The preparation and process involves many factors and parameters specifically in fabricating hollow fibre membrane. In this study, dope solution factor in the process of fabricating hollow fibre membrane were explored. The effects of polymer concentration and polyvinylpyrrolidone (PVP) as additive in the dope solution on the morphology and separation performance were found able to produced high porous membranes, well interconnected pores and surface properties. Employing polyethersulfone (PES) as polymer, hollow fibre membranes were fabricated using N-methyl-2-pyrrolidone (NMP) as solvent and using water as the external coagulant. Finally the fabricated ultrafiltration membranes were characterized and evaluated based on solute transport concentration (sodium chloride) and pure water permeation properties.

  20. Anodic Oxide Thin Films on Iron in Neutral Borate-Boric-Acid Solution with and without Chloride Ion

    NASA Astrophysics Data System (ADS)

    Tokunaga, Katsushi

    1982-12-01

    The composition of anodic oxide films formed on iron in neutral borate-boric-acid solutions with and without chloride ions was examined by sensitive ESCA, IMMA, electron diffraction and FT-IR spectroscopy. In general, the oxide thin film consisted of a two layer structure of “Fe3O4 or γ-Fe2O3” next to the metal and “γ-FeOOH or ferric boron hydroxo complexes such as Fe(OH)(BO2)2 or FeOHB4O7” at the oxide solution interface, with iron in its trivalent state. The outermost part of the film contained minor impurities or contaminations such as boron, calcium and silicon, all of which were in the oxide state. The thickness of the passive film was about 20-50 Å. The addition of the chloride ion to borate solutions increases the amount of γ-FeOOH present. Corrosion pits are preferentially nucleated at inclusions such as Si and Mn.

  1. Porous polymer nanostructures fabricated by the surface-induced phase separation of polymer solutions in anodic aluminum oxide templates.

    PubMed

    Wei, Tzu-Hui; Chi, Mu-Huan; Tsai, Chia-Chan; Ko, Hao-Wen; Chen, Jiun-Tai

    2013-08-13

    We study the formation of porous polymer nanostructures fabricated by the surface-induced phase separation of polymer solutions in anodic aluminum oxide (AAO) templates. Poly(methyl methacrylate) (PMMA) and tetrahydrofuran (THF) are used to investigate the evolution process of the surface-induced phase separation. With the longer immersion time of the AAO template in the polymer solution, the size of the solvent-rich droplet is increased by the coarsening process, resulting in the formation of porous polymer nanostructures. The coarsening mechanism is further evaluated by changing the experimental parameters including the immersion time, the polymer concentration, the polymer molecular weight, and the solvent quality. Under conditions in which polymer solutions have higher viscosities, the coarsening process is slowed down and the formation of the porous nanostructures is prohibited. The prevention of the porous nanostructures can also be realized by adding water to the PMMA/THF solution before the immersion process.

  2. Evidence of mass exchange between inside and outside of sonoluminescing bubble in aqueous solution of terbium chloride

    NASA Astrophysics Data System (ADS)

    Liang, Jinfu; Chen, Weizhong; Wang, Xun; Yang, Jing; Chen, Zhan

    2016-12-01

    Spectra of single-bubble sonoluminescence (SBSL) were obtained for Tb3+ ions emission lines from bubbles in an aqueous solution of terbium chloride (TbCl3). The spectra provide experimental evidence to prove that an air bubble driven by strong ultrasound will not eventually become a rectified pure argon bubble, which is not as predicted by the argon rectification hypothesis. The time-resolved spectra of SBSL show a mass exchange of material such as Tb3+ ions between the inside and outside of the bubble. With increasing sound pressure, the rate of mass exchange and the SBSL intensity increases.

  3. Shock Hugoniot and equations of states of water, castor oil, and aqueous solutions of sodium chloride, sucrose and gelatin

    NASA Astrophysics Data System (ADS)

    Gojani, A. B.; Ohtani, K.; Takayama, K.; Hosseini, S. H. R.

    2016-01-01

    This paper reports a result of experiments for the determination of reliable shock Hugoniot curves of liquids, in particular, at relatively low pressure region, which are needed to perform precise numerical simulations of shock wave/tissue interaction prior to the development of shock wave related therapeutic devices. Underwater shock waves were generated by explosions of laser ignited 10 mg silver azide pellets, which were temporally and spatially well controlled. Measuring temporal variation of shock velocities and over-pressures in caster oil, aqueous solutions of sodium chloride, sucrose and gelatin with various concentrations, we succeeded to determine shock Hugoniot curves of these liquids and hence parameters describing Tait type equations of state.

  4. Effect of Chloride Precursors on the Stability of Solution-Processed Indium Zinc Oxide Thin-Film Transistors

    NASA Astrophysics Data System (ADS)

    Lee, Dong Hee; Park, Sung Min; Yang, Jung Il; Cho, Dong Kyu; Woo, Sang Hyun; Lim, Yoo Sung; Kuk Kim, Dae; Yi, Moonsuk

    2013-10-01

    In this experiment, solution-processed indium zinc oxide (IZO) films were prepared by spin-coating the films as an active layer in thin-film transistors (TFTs). These films were coated with nitrate and a mixture of acetate- and chloride-based precursors to allow the IZO films to contain indium and zinc components. The solution-processed IZO-based TFT fabricated using a zinc acetate precursor for the IZO films exhibited a mobility of 2.83 cm2 V-1 s-1, an on/off current ratio of ˜1×105, and a subthreshold swing value of 2.48 V/dec. The IZO-TFT with the zinc chloride precursor exhibited a mobility of 4.37 cm2 V-1 s-1, an on/off current ratio of ˜1×103, and a subthreshold swing value of 6.44 V/dec. In comparison, the IZO-TFT with a mixture of zinc acetate and chloride precursors exhibited a mobility of 1.45 cm2 V-1 s-1, an on/off current ratio of ˜1×105, and a subthreshold swing value of 1.83 V/dec. The first two devices suffered from a large threshold voltage (Vth) shift, >7 and >6 V, respectively, after a gate voltage of 20 V was applied for 2 h. In contrast, the device fabricated using the mixed precursors showed a higher stability, shifting about 1.7 V under the same stress conditions.

  5. Removal of chloride ion from aqueous solution by ZnAl-NO(3) layered double hydroxides as anion-exchanger.

    PubMed

    Lv, Liang; Sun, Peide; Gu, Zhengyu; Du, Hangeng; Pang, Xiangjun; Tao, Xiaohong; Xu, Rufeng; Xu, Lili

    2009-01-30

    The layered double hydroxides (LDHs) containing nitrate as the interlayer anion has a high anion-exchange capacity in the presence of appropriate anions. In the light of this, ZnAl-NO(3) LDHs have been employed to remove chloride ion from aqueous solution in a batch mode. The influences of conditions for chloride ion uptake, including dosage of LDHs, pH of aqueous solution, and temperature on anion-exchange have been investigated, respectively. The thermodynamic parameters including Gibbs free energy (DeltaG(0)), standard enthalpy change (DeltaH(0)), and standard entropy change (DeltaS(0)) for the process were calculated using the Langmuir constants. It was found from kinetics test that the pseudo-second order kinetics model could be used to well describe the uptake process. An E(a) value of 10.27 kJ/mol provides evidence the anion-exchange process. The explanation of anion-exchange phenomenon has also been supported by X-ray diffraction and FT-IR spectra.

  6. Quantitative Analysis of Volatile Impurities in Diallyldimethylammonium Chloride Monomer Solution by Gas Chromatography Coupled with Liquid-Liquid Extraction

    PubMed Central

    Wang, Haiying; Wang, Weixin

    2017-01-01

    The quantitative analysis method for volatile impurities in diallyldimethylammonium chloride (DADMAC) monomer solution was established in this paper. The volatile impurities were quantitatively analyzed with trichloromethane as extraction solvent and n-hexane as internal standard by using gas chromatography (GC) coupled with solvent extraction, and the chromatographic conditions, quantitative methods, and extraction conditions were systematically investigated in detail. The results showed that excellent linear relationships of 5 volatile impurities (dimethylamine, allyldimethylamine, allyl chloride, allyl alcohol, and allyl aldehyde) were obtained in the range of 1–100 mg·L−1. The method also showed good specificity, recovery (95.0%–107.5%), and relative standard deviation (RSD, 1.40%–7.67%). This method could accurately detect the whole volatile impurities in DADMAC monomer solution quantitatively in one time with a low detection limit. Furthermore, this method is conducive to the preparation of highly pure DADMAC monomer and the development of national and international standards of the DADMAC monomer product quality, and the results could provide a strong foundation for the regulation and mechanism research of impurities on monomer reactivity in polymerization. PMID:28243255

  7. The role of macrocyclic compounds in the extraction and possible separation of platinum and rhodium from chloride solutions

    NASA Astrophysics Data System (ADS)

    Jyothi, Rajesh Kumar; Lee, Jin-Young

    2016-06-01

    Macrocyclic compounds (crown ethers), specifically 18-crown-6 (18-C-6), benzo-15-crown-5 (B-15-C-5), di-benzo-18-crown-6 (DB-18-C-6) and di-cyclohexano-18-crown-6 (DC-18C-6), are used as extractants as well as synergists with amine-group extractants. Platinum and rhodium belong to platinum-group metals (PGMs) and have very similar ionic radii and similar properties. The separation of PGMs is most useful for the preparation of functional materials. Macrocyclic compounds are tested for platinum and rhodium separation and are found to achieve marginal separation. Amines (used as extractants) are paired with macrocyclic compounds (used as synergists), and the separation factor between platinum and rhodium is increased with synergistic enhancement from a chloride solution. The present study discusses extraction chemistry, separation factors and the synergy between platinum and rhodium from chloride solutions. To ensure accurate data, the aqueous samples in this study are analyzed using an inductively coupled plasma optical emission spectrometer (ICP-OES).

  8. Cation effects on interfacial water organization of aqueous chloride solutions. I. Monovalent cations: Li+, Na+, K+, and NH4(+).

    PubMed

    Hua, Wei; Verreault, Dominique; Huang, Zishuai; Adams, Ellen M; Allen, Heather C

    2014-07-17

    The influence of monovalent cations on the interfacial water organization of alkali (LiCl, NaCl, and KCl) and ammonium chloride (NH4Cl) salt solutions was investigated using surface-sensitive conventional vibrational sum frequency generation (VSFG) and heterodyne-detected (HD-)VSFG spectroscopy. It was found in the conventional VSFG spectra that LiCl and NH4Cl significantly perturb water’s hydrogen-bonding network. In contrast, NaCl and KCl had little effect on the interfacial water structure and exhibited weak concentration dependency. The Im χs(2)(ωIR) spectra from HD-VSFG further revealed that, for all chloride solutions, the net transition dipole moments of hydrogen-bonded water molecules (O → H) are oriented more toward the vapor phase relative to neat water. This suggests the presence of an interfacial electric field generated from the formation of an ionic double layer in the interfacial region with a distribution of Cl(-) ions located above the countercations, in agreement with predictions from MD simulations. The magnitude of this electric field shows a small but definite cation specificity and follows the order Li(+) ≈ Na(+) > NH4(+) > K(+). The observed trend was found to be in good agreement with previously published surface potential data.

  9. Human body frequency modulation by 0.9% sodium chloride solutions: a new paradigm and perspective for human health.

    PubMed

    Sudan, B J

    2000-08-01

    This case study demonstrates that the normal human body frequency, which can be disturbed by electromagnetic influences of the environment, can be modulated by 0.9% sodium chloride solutions (physiological saline) and that occurrence of allergic reactions have subsequently been suppressed as a result of this modulation. The use of distilled water as control showed no effect on occurrence of allergic reactions. Further observations on the growth of various plants in a greenhouse exposed to various geomagnetic fields support the previous observations on humans. The neutralization of electromagnetic influences on humans using 0.9% sodium chloride solution or by enclosure of plants within a copper wire Faraday cage resulting in a normal and uniform growth of plants as compared with disturbed and irregular growth in unenclosed controls, is demonstrated. These original observations propose a new strategy to suppress or prevent allergic reactions and possibly other effects observed in various human pathologies in relation to a disturbance of human body frequencies. It is hypothesized that the double helix structure of desoxyribonucleic acid (DNA) could be modified by environmental electromagnetic fields and that disresonance between the two chains of DNA could lead to the expression of specific pathology.

  10. The role of macrocyclic compounds in the extraction and possible separation of platinum and rhodium from chloride solutions

    PubMed Central

    Jyothi, Rajesh Kumar; Lee, Jin-Young

    2016-01-01

    Macrocyclic compounds (crown ethers), specifically 18-crown-6 (18-C-6), benzo-15-crown-5 (B-15-C-5), di-benzo-18-crown-6 (DB-18-C-6) and di-cyclohexano-18-crown-6 (DC-18C-6), are used as extractants as well as synergists with amine-group extractants. Platinum and rhodium belong to platinum-group metals (PGMs) and have very similar ionic radii and similar properties. The separation of PGMs is most useful for the preparation of functional materials. Macrocyclic compounds are tested for platinum and rhodium separation and are found to achieve marginal separation. Amines (used as extractants) are paired with macrocyclic compounds (used as synergists), and the separation factor between platinum and rhodium is increased with synergistic enhancement from a chloride solution. The present study discusses extraction chemistry, separation factors and the synergy between platinum and rhodium from chloride solutions. To ensure accurate data, the aqueous samples in this study are analyzed using an inductively coupled plasma optical emission spectrometer (ICP-OES). PMID:27283394

  11. Electrochemical corrosion and modeling studies of types 7075 and 2219 aluminum alloys in a nitric acid + ferric sulfate deoxidizer solution

    NASA Astrophysics Data System (ADS)

    Savas, Terence P.

    The corrosion behavior of types 7075-T73 and 2219-T852 high strength aluminum alloys have been investigated in a HNO3 + Fe2(SO 4)3 solution. The materials are characterized in the time domain using the electrochemical noise resistance parameter (Rn) and in the frequency-domain using the spectral noise impedance parameter ( Rsn). The Rsn parameter is derived from an equivalent electrical circuit model that represents the corrosion test cell schematic used in the present study. These calculated parameters are correlated to each other, and to corresponding scanning electron microscopy (SEM) examinations of the corroded surfaces. In addition, energy dispersive spectroscopy (EDS) spectra are used in conjunction with SEM exams for particle mapping and identification. These constituent particles are characterized with respect to their size and composition and their effect on the localized corrosion mechanisms taking place. Pitting mechanisms are identified as 'circumferential' where the particles appeared noble with respect to the aluminum matrix and by 'selective dissolution' where they are anodic to the aluminum matrix. The electrochemical data are found to be in good agreement with the surface examinations. Specifically, the electrochemical parameters Rn and Rsn were consistent in predicting the corrosion resistance of 7075-T73 to be lower than for the 2219-T852 alloy. Other characteristic features used in understanding the corrosion mechanisms include the open circuit potential (OCP) and coupling-current time records.

  12. Effect of the salt-induced micellar microstructure on the nonlinear shear flow behavior of ionic cetylpyridinium chloride surfactant solutions

    NASA Astrophysics Data System (ADS)

    Gaudino, D.; Pasquino, R.; Kriegs, H.; Szekely, N.; Pyckhout-Hintzen, W.; Lettinga, M. P.; Grizzuti, N.

    2017-03-01

    The shear flow dynamics of linear and branched wormlike micellar systems based on cetylpyridinium chloride and sodium salicylate in brine solution is investigated through rheometric and scattering techniques. In particular, the flow and the structural flow response are explored via velocimetry measurements and rheological and rheometric small-angle neutron scattering (SANS) experiments, respectively. Although all micellar solutions display a similar shear thinning behavior in the nonlinear regime, the experimental results show that shear banding sets in only when the micelle contour length L ¯ is sufficiently long, independent of the nature of the micellar connections (either linear or branched micelles). Using rheometric SANS, we observe that the shear banding systems both show very similar orientational ordering as a function of Weissenberg number, while the short branched micelles manifest an unexpected increase of ordering at very low Weissenberg numbers. This suggests the presence of an additional flow-induced relaxation process that is peculiar for branched systems.

  13. Structural, optical, thermal, mechanical and dielectrical characterizations of γ-glycine crystals grown in strontium chloride solution

    NASA Astrophysics Data System (ADS)

    Helina, B.; Selvarajan, P.; Rose, A. S. J. Lucia

    2012-05-01

    γ-glycine (GG) was synthesized from α-glycine in an aqueous solution of strontium chloride. A solubility study of the synthesized GG sample was conducted at various temperatures ranging from 30 to 55 °C. The saturated solution of GG was prepared using solubility data, and single crystals of GG were grown over a period of three weeks by the slow evaporation method at room temperature. The grown GG crystals were characterized by single-crystal x-ray diffraction analysis, UV-visible transmittance studies, thermogravimetric/differential thermal analysis studies, dielectric studies and Fourier transform infrared studies. The mechanical behavior of the crystals was assessed by Vickers microhardness measurements. The second-harmonic generation efficiency of the sample was measured using a Nd:YAG laser and the value was observed to be larger than that of potassium dihydrogen orthophosphate (KDP).

  14. Method for calcining nuclear waste solutions containing zirconium and halides

    DOEpatents

    Newby, Billie J.

    1979-01-01

    A reduction in the quantity of gelatinous solids which are formed in aqueous zirconium-fluoride nuclear reprocessing waste solutions by calcium nitrate added to suppress halide volatility during calcination of the solution while further suppressing chloride volatility is achieved by increasing the aluminum to fluoride mole ratio in the waste solution prior to adding the calcium nitrate.

  15. Pitting and crevice corrosion of stainless steels in ammonium chloride solutions

    SciTech Connect

    Forsen, O.; Aromaa, J.; Virtanen, J.; Tavi, M.

    1995-09-01

    Carbon steel is the most commonly used construction material in oil refining. Ammonium chloride deposition is a well known problem in oil refining. When these deposits form in a moist environment, they are corrosive to carbon steel. When unexpected corrosion problems are faced the material is often changed zn to alloys like stainless steels. The main drawback of stainless steels is that they are prone to different forms of localized corrosion, especially in the presence of halides. In this paper the use of electrochemical measurements to study the corrosion resistance of stainless steels is discussed.

  16. Self-organization of hydrogen gas bubbles rising above laser-etched metallic aluminum in a weakly basic aqueous solution.

    PubMed

    Barmina, E V; Kuzmin, P G; Shafeev, G A

    2011-10-01

    Self-organization of hydrogen bubbles is reported under etching of metallic Aluminum in a weakly basic solution. The ascending gas bubbles drift to the areas with higher density of bubbles. As a result, ascending bubbles form various stationary structures whose symmetry is determined by the symmetry of the etched area. Bubbles are aligned along the bisectors of the contour of the etched area. The special laser-assisted profiling of the etched area in shape of a vortex induces a torque in the fluid above the etched area. The process is interpreted on the basis of Bernoulli equation.

  17. Raman OD stretching spectral differences between aqueous and alcoholic tetraalkylammonium chloride solutions

    NASA Astrophysics Data System (ADS)

    Hidaka, Fumi; Kanno, Hitoshi

    2003-09-01

    Raman OD stretching spectra were measured for aqueous and alcoholic R 4NCl solutions in both liquid state at room temperature and glassy state at liquid nitrogen temperature (alcohol=methanol and ethanol, R=alkyl group: methyl, ethyl and n-propyl). Comparison of the spectra indicates that enhancement of the low frequency region is more pronounced for the glassy aqueous solution than the corresponding alcohol solution. It is suggested that hydrophobic hydration plays a role in the strengthening of hydrogen bonds around an apolar solute (group) at low temperatures in aqueous solution system.

  18. Regioselective organocatalysis: a theoretical prediction of the selective rate acceleration of the SN2 reaction between an acetate ion and primary alkyl chlorides in DMSO solution.

    PubMed

    Pliego, Josefredo R

    2006-05-07

    High level ab initio calculations, including the solvent effect through a continuum solvation model, predict that 1,4-benzenedimethanol is able to catalyse the S(N)2 reaction between an acetate ion and primary alkyl chlorides in dimethyl sulfoxide solution. The catalysis takes place through two selective hydrogen bonds to the transition state. However, for secondary alkyl chlorides the catalysis is not effective due to steric repulsion and desolvation. This effect induces regioselective control of S(N)2 esterification reactions.

  19. A Fiber-Optic Sensor Using an Aqueous Solution of Sodium Chloride to Measure Temperature and Water Level Simultaneously

    PubMed Central

    Yoo, Wook Jae; Sim, Hyeok In; Shin, Sang Hun; Jang, Kyoung Won; Cho, Seunghyun; Moon, Joo Hyun; Lee, Bongsoo

    2014-01-01

    A fiber-optic sensor system using a multiplexed array of sensing probes based on an aqueous solution of sodium chloride (NaCl solution) and an optical time-domain reflectometer (OTDR) for simultaneous measurement of temperature and water level is proposed. By changing the temperature, the refractive index of the NaCl solution is varied and Fresnel reflection arising at the interface between the distal end of optical fiber and the NaCl solution is then also changed. We measured the modified optical power of the light reflected from the sensing probe using a portable OTDR device and also obtained the relationship between the temperature of water and the optical power. In this study, the water level was simply determined by measuring the signal difference of the optical power due to the temperature difference of individual sensing probes placed inside and outside of the water. In conclusion, we demonstrate that the temperature and water level can be obtained simultaneously by measuring optical powers of light reflected from sensing probes based on the NaCl solution. It is anticipated that the proposed fiber-optic sensor system makes it possible to remotely monitor the real-time change of temperature and water level of the spent fuel pool during a loss of power accident. PMID:25310471

  20. Slow strain rate fracture of high-strength steel at controlled electrochemical potentials in ammonium chloride, potassium chloride, and ammonium nitrate solutions

    SciTech Connect

    Nguyen, D.T.; Nichols, D.E.; Daniels, R.D.

    1992-08-15

    Slow strain rate testing has been undertaken to determine the effects of individual chemical species on the fracture process of high-strength 4340 steel. Test environments included potassium chloride, ammonium nitrate, and ammonium chloride at concentrations from 0.001 to 1.0 mole por liter at ambient temperature. Tests were performed at cathodic and anodic controlled potentials, as well as at the open-circuit potential, to delineate the stress corrosion cracking range.

  1. Assessing the effectiveness of 30% sodium chloride aqueous solution for the preservation of fixed anatomical specimens: a 5-year follow-up study.

    PubMed

    de Oliveira, Fabrício Singaretti

    2014-07-01

    Anatomical specimens used in human or veterinary anatomy laboratories are usually prepared with formaldehyde (a cancerous and teratogenic substance), glycerin (an expensive and viscous fluid), or ethanol (which is flammable). This research aimed to verify the viability of an aqueous 30% sodium chloride solution for preservation of anatomical specimens previously fixed with formaldehyde. Anatomical specimens of ruminant, carnivorous, equine, swine and birds were used. All were previously fixed with an aqueous 20% formaldehyde solution and held for 7 days in a 10% aqueous solution of the same active ingredient. During the first phase of the experiment, small specimens of animal tissue previously fixed in formaldehyde were distributed in vials with different concentrations of formaldehyde, with or without 30% sodium chloride solution, a group containing only 30% sodium chloride, and a control group containing only water. During this phase, no contamination was observed in any specimen containing 30% sodium chloride solution, whether alone or in combination with different concentrations of formaldehyde. In the second phase of the experiment, the 30% sodium chloride solution, found to be optimal in the first phase of the experiment, was tested for its long-term preservation properties. For a period of 5 years, the preserved specimens were evaluated three times a week for visual contamination, odors, and changes in color and texture. There was no visual contamination or decay found in any specimen. Furthermore, no strange odors, or changes in color or softness were noted. The 30% sodium chloride solution was determined to be effective in the preservation of anatomic specimens previously fixed in formaldehyde.

  2. Assessing the effectiveness of 30% sodium chloride aqueous solution for the preservation of fixed anatomical specimens: a 5-year follow-up study

    PubMed Central

    de Oliveira, Fabrício Singaretti

    2014-01-01

    Anatomical specimens used in human or veterinary anatomy laboratories are usually prepared with formaldehyde (a cancerous and teratogenic substance), glycerin (an expensive and viscous fluid), or ethanol (which is flammable). This research aimed to verify the viability of an aqueous 30% sodium chloride solution for preservation of anatomical specimens previously fixed with formaldehyde. Anatomical specimens of ruminant, carnivorous, equine, swine and birds were used. All were previously fixed with an aqueous 20% formaldehyde solution and held for 7 days in a 10% aqueous solution of the same active ingredient. During the first phase of the experiment, small specimens of animal tissue previously fixed in formaldehyde were distributed in vials with different concentrations of formaldehyde, with or without 30% sodium chloride solution, a group containing only 30% sodium chloride, and a control group containing only water. During this phase, no contamination was observed in any specimen containing 30% sodium chloride solution, whether alone or in combination with different concentrations of formaldehyde. In the second phase of the experiment, the 30% sodium chloride solution, found to be optimal in the first phase of the experiment, was tested for its long-term preservation properties. For a period of 5 years, the preserved specimens were evaluated three times a week for visual contamination, odors, and changes in color and texture. There was no visual contamination or decay found in any specimen. Furthermore, no strange odors, or changes in color or softness were noted. The 30% sodium chloride solution was determined to be effective in the preservation of anatomic specimens previously fixed in formaldehyde. PMID:24762210

  3. Influence of high temperature on corrosion behavior of 304 stainless steel in chloride solutions

    NASA Astrophysics Data System (ADS)

    Ahmed, Saad R.

    2016-11-01

    Despite the excellent performance of stainless steel in diverse application, there are media of exposure may accelerate failure of several stainless steel alloys. The possibility of this failure has to be examined by measuring the effective parameters that may result in corrosion at different rates. The present study has been conducted to examine the effect of exposing specimens of 304 stainless steel to 0.5, 1.0, 1.5 and 2.0 M chloride concentration and 70, 80, and 90 °C. Electrochemical technique of measuring the potentials and currency of the examined system has been used to collect the corrosion data. Microstructure of the specimens is examined using Scanning Electron Microscopy and X- Ray Diffraction. Both of these tests revealed no serious phase change due to exposure even at severe conditions. The potentials gained show significant effect of the operation conditions.

  4. Viscosities of the ternary solution dimethyl sulfoxide/water/sodium chloride at subzero temperatures and their application in cryopreservation.

    PubMed

    Zhang, Shaozhi; Yu, Xiaoyi; Chen, Zhaojie; Chen, Guangming

    2013-04-01

    Vitrification is considered as the most promising method for long-term storage of tissues and organs. An effective way to reduce the accompanied cryoprotectant (CPA) toxicity, during CPA addition/removal, is to operate at low temperatures. The permeation process of CPA into/out of biomaterials is affected by the viscosity of CPA solution, especially at low temperatures. The objective of the present study is to measure the viscosity of the ternary solution, dimethyl sulfoxide (Me2SO)/water/sodium chloride (NaCl), at low temperatures and in a wide range of concentrations. A rotary viscometer coupled with a low temperature thermostat bath was used. The measurement was carried out at temperatures from -10 to -50°C. The highest mass fraction of Me2SO was 75% (w/w) and the lowest mass fraction of Me2SO was the value that kept the solution unfrozen at the measurement temperature. The concentration of NaCl was kept as a constant [0.85% (w/w), the normal salt content of extracellular fluids]. The Williams-Landel-Ferry (WLF) model was employed to fit the obtained viscosity data. As an example, the effect of solution viscosity on modeling the permeation of Me2SO into articular cartilage was qualitatively analyzed.

  5. Aluminum reference electrode

    DOEpatents

    Sadoway, D.R.

    1988-08-16

    A stable reference electrode is described for use in monitoring and controlling the process of electrolytic reduction of a metal. In the case of Hall cell reduction of aluminum, the reference electrode comprises a pool of molten aluminum and a solution of molten cryolite, Na[sub 3]AlF[sub 6], wherein the electrical connection to the molten aluminum does not contact the highly corrosive molten salt solution. This is accomplished by altering the density of either the aluminum (decreasing the density) or the electrolyte (increasing the density) so that the aluminum floats on top of the molten salt solution. 1 fig.

  6. Aluminum reference electrode

    DOEpatents

    Sadoway, Donald R.

    1988-01-01

    A stable reference electrode for use in monitoring and controlling the process of electrolytic reduction of a metal. In the case of Hall cell reduction of aluminum, the reference electrode comprises a pool of molten aluminum and a solution of molten cryolite, Na.sub.3 AlF.sub.6, wherein the electrical connection to the molten aluminum does not contact the highly corrosive molten salt solution. This is accomplished by altering the density of either the aluminum (decreasing the density) or the electrolyte (increasing the density) so that the aluminum floats on top of the molten salt solution.

  7. Corrosion cracking of 03N18K1M3TYu and 02N12Kh5M3 maraging steels in chloride solutions

    SciTech Connect

    Pavlov, V.N.; Chumalo, G.V.; Vereshchagin, A.N.; Melekhov, R.K.

    1987-07-01

    The authors investigate the electrochemical behavior in 0.5% NaCl solution and 42% MgCl/sub 2/ solution and the tendency toward corrosion cracking was determined in boiling 0.5% chloride solution of the cobalt-containing maraging steels in the title. Weld specimens and specimens of the base metal of 03N18K1M3TYu steel were tested in 3% NaCl solution for resistance to corrosion cracking. Additional investigations were made of specimens of that steel with previously created fatigue cracks of the base metal and the weld specimens in 3% NaCl solutions, since that steel is a promising material for structures operating in sea water and low concentration chloride solutions.

  8. Corrosion Behavior of Alloy 22 in Chloride Solutions Containing Organic Acids

    SciTech Connect

    Carranza, R M; Giordano, C M; Rodr?guez, M A; Rebak, R B

    2005-11-04

    Alloy 22 (N06022) is a nickel based alloy containing alloying elements such as chromium, molybdenum and tungsten. It is highly corrosion resistant both under reducing and under oxidizing conditions. Electrochemical studies such as electrochemical impedance spectroscopy (EIS) were performed to determine the corrosion behavior of Alloy 22 in 1M NaCl solutions at various pH values from acidic to neutral at 90 C. Tests were also carried out in NaCl solutions containing oxalic acid or acetic acid. It is shown that the corrosion rate of Alloy 22 was higher in a solution containing oxalic acid than in a solution of the same pH acidified with HCl. Acetic acid was not corrosive to Alloy 22. The corrosivity of oxalic acid was attributed to its capacity to form stable complex species with metallic cations from Alloy 22.

  9. Thermodynamics of aqueous borate solutions I. Mixture of boric acid with sodium or potassium borate and chloride

    SciTech Connect

    Simonson, J.M.; Roy, R.N.; Roy, L.N.; Johnson, D.A.

    1987-10-01

    Potentials for the cell without liquid junction H/sub 2/, Ptlt. slashB(OH)/sub 3/(m/sub 1/),MB(OH)/sub 4/(m/sub 2/),MCl(m/sub 3/)lt. slashAgCl,Ag where M is sodium or potassium are reported over a range of ionic strength to I = 3 mol-kg/sup -1/ at 5 to 55/sup 0/C. Total boron concentration in the solutions was restricted to low levels to minimize formation of polynuclear boron species. Cell potentials are treated with the Pitzer ion interaction treatment for mixed electrolytes, with linear ionic strength dependence assumed for the activity coefficient of undissociated boric acid. Trace activity coefficients of sodium and potassium borates in chloride media are calculated at various temperatures.

  10. Characterization of Cellulose regenerated from solutions of pine and eucalyptus woods in 1-allyl-3-methilimidazolium chloride.

    PubMed

    Casas, A; Alonso, M V; Oliet, M; Santos, T M; Rodriguez, F

    2013-02-15

    Cellulose is currently separated from lignocellulosic materials using non-environmentally friendly processes. The development of new methods for treating biomass and separating cellulose remains a challenge and would be very useful in the context of the biorefinery philosophy. In this work, cellulose has been regenerated from solutions of Pinus radiata and Eucalyptus globulus woods in 1-allyl-3-methylimidazolium chloride. Wood dissolution was performed in a microwave oven at 120 °C for 20 min. Cellulose was characterized and compared to the reference material, microcrystalline cellulose (MCC). Regenerated celluloses showed lower crystallinity and thermal stability than MCC, although the ash contents at 400 °C were higher than in MCC. The regenerated celluloses were obtained without lignin and almost free from hemicellulose. Furthermore, cellulose was not significantly degraded in the dissolution process of both woods. The insoluble solids showed higher content of lignin and hemicellulose than the raw materials.

  11. Corrosion behavior of ruthenium oxide-titanium anodes during production of sodium chlorate by electrolysis of chloride-chlorate solutions

    SciTech Connect

    Uzbekov, A.A.; Klement 'pva, V.S.; Kubasov, V.L.; Lambrev, V.G.

    1985-09-01

    The authors studied the influence of specific factors in chlorate electrilysis on the corrosion behavior of ROTA. The technique used in the investigation was based on neutron activation of the test specimens followed by corrosion tests. Figures show the dependence rate of ruthenium dissolution on the sodium chloride production during production of chlorate by electrolysis with ROTA, and dependence of the rate of ruthenium dissolution and of the rate of oxygen evolution during polarization of ROTA. Over the entire range of ROTA potentials studied the process of oxygen evolution conforms to the Tafel relationship. The rate of ruthenium dissolution in chlorate solution rises by more than 4 orders of magnitude with increase of the ROTA potential.

  12. Blue-Green Color Tunable Solution Processable Organolead Chloride-Bromide Mixed Halide Perovskites for Optoelectronic Applications.

    PubMed

    Sadhanala, Aditya; Ahmad, Shahab; Zhao, Baodan; Giesbrecht, Nadja; Pearce, Phoebe M; Deschler, Felix; Hoye, Robert L Z; Gödel, Karl C; Bein, Thomas; Docampo, Pablo; Dutton, Siân E; De Volder, Michael F L; Friend, Richard H

    2015-09-09

    Solution-processed organo-lead halide perovskites are produced with sharp, color-pure electroluminescence that can be tuned from blue to green region of visible spectrum (425-570 nm). This was accomplished by controlling the halide composition of CH3NH3Pb(BrxCl1-x)3 [0 ≤ x ≤ 1] perovskites. The bandgap and lattice parameters change monotonically with composition. The films possess remarkably sharp band edges and a clean bandgap, with a single optically active phase. These chloride-bromide perovskites can potentially be used in optoelectronic devices like solar cells and light emitting diodes (LEDs). Here we demonstrate high color-purity, tunable LEDs with narrow emission full width at half maxima (FWHM) and low turn on voltages using thin-films of these perovskite materials, including a blue CH3NH3PbCl3 perovskite LED with a narrow emission FWHM of 5 nm.

  13. ZnO Nanorods via Spray Deposition of Solutions Containing Zinc Chloride and Thiocarbamide.

    PubMed

    Dedova, Tatjana; Volobujeva, Olga; Klauson, Jelena; Mere, Arvo; Krunks, Malle

    2007-07-19

    In this work we present the results on formation of ZnO nanorods prepared by spray of aqueous solutions containing ZnCl2and thiocarbamide (tu) at different molar ratios. It has been observed that addition of thiocarbamide into the spray solution has great impact on the size, shape and phase composition of the ZnO crystals. Obtained layers were characterized by scanning electron microscopy (SEM) equipped with energy selected backscattered electron detection system (ESB), X-ray diffraction (XRD) and photoluminescence spectroscopy (PL). Small addition of thiocarbamide into ZnCl2solution (ZnCl2:tu = 1:0.25) supports development of significantly thinner ZnO nanorods with higher aspect ratio compared to those obtained from ZnCl2solution. Diameter of ZnO rods decreases from 270 to 100 nm and aspect ratio increases from ∼2.5 to 12 spraying ZnCl2and ZnCl2:tu solutions, respectively. According to XRD, well crystallized (002) orientated pure wurtzite ZnO crystals have been formed. However, tiny 'spot'-like formations of ZnS were detected on the side planes of hexagonal rods prepared from the thiocarbamide containing solutions. Being adsorbed on the side facets of the crystals ZnS inhibits width growth and promotes longitudinalc-axis growth.

  14. ZnO Nanorods via Spray Deposition of Solutions Containing Zinc Chloride and Thiocarbamide

    PubMed Central

    2007-01-01

    In this work we present the results on formation of ZnO nanorods prepared by spray of aqueous solutions containing ZnCl2and thiocarbamide (tu) at different molar ratios. It has been observed that addition of thiocarbamide into the spray solution has great impact on the size, shape and phase composition of the ZnO crystals. Obtained layers were characterized by scanning electron microscopy (SEM) equipped with energy selected backscattered electron detection system (ESB), X-ray diffraction (XRD) and photoluminescence spectroscopy (PL). Small addition of thiocarbamide into ZnCl2solution (ZnCl2:tu = 1:0.25) supports development of significantly thinner ZnO nanorods with higher aspect ratio compared to those obtained from ZnCl2solution. Diameter of ZnO rods decreases from 270 to 100 nm and aspect ratio increases from ∼2.5 to 12 spraying ZnCl2and ZnCl2:tu solutions, respectively. According to XRD, well crystallized (002) orientated pure wurtzite ZnO crystals have been formed. However, tiny ‘spot’—like formations of ZnS were detected on the side planes of hexagonal rods prepared from the thiocarbamide containing solutions. Being adsorbed on the side facets of the crystals ZnS inhibits width growth and promotes longitudinalc-axis growth. PMID:21794191

  15. Influence of the chloride ion concentration on the corrosion of high-purity Mg, ZE41 and AZ91 in buffered Hank's solution.

    PubMed

    Taltavull, C; Shi, Z; Torres, B; Rams, J; Atrens, A

    2014-02-01

    This research studied the influence of the chloride ion concentration on the corrosion behaviour of high-purity magnesium (Mg) and two Mg alloys in Hank's solution, using hydrogen evolution and weight loss. A buffer based on CO2 and NaHCO3 was used to maintain the pH constant. The corrosion behaviour was governed by a partially protective surface film, and film breakdown by the chloride ions. The carbonated calcium phosphate layer that formed in Hank's solution was important in determining the protective properties of the surface film.

  16. Disinfection of contaminated equipment: evaluation of benzalkonium chloride exposure time and solution age and the ability of air-drying to eliminate Flavobacterium psychrophilum.

    PubMed

    Oplinger, Randall W; Wagner, Eric

    2010-12-01

    Disinfection of equipment that comes in contact with fish can help to minimize the spread of Flavobacterium psychrophilum (the etiological agent of bacterial coldwater disease) within and among fish culture facilities. We present the results of three studies that evaluated the potential use of benzalkonium chloride and air-drying to kill surface-attached F. psychrophilum. In the first study, we established a vat with a 600-mg/L benzalkonium chloride solution and sampled this solution 0, 14, 35, 56, 70, and 84 d after creation. The solution was kept outdoors and subjected to typical hatchery use. Plastic test strips were dipped in a solution containing F. psychrophilum and were then immersed in benzalkonium chloride for 0, 1, 10, 30, or 60 min. The strips were then rinsed with sterile water and streaked across a plate containing tryptone yeast extract salts (TYES) medium. No culturable bacteria were detected from any strips immersed for 10, 30, or 60 min. Bacteria were detected on 17% of the strips that were immersed for 1 min. The age of the benzalkonium chloride solution had no effect on disinfection ability. In the second study, plastic strips were immersed in a solution containing F. psychrophilum and then were dipped in a 600-mg/L benzalkonium chloride solution for 10 s. The strips were then air-dried for 1 h and were streaked onto TYES medium. No bacterial growth was observed from any strips in the second experiment. The third study determined whether air-drying alone was sufficient to kill F. psychrophilum. Plastic strips were dipped in a solution containing F. psychrophilum; were allowed to dry at room temperature for 0, 24, 48, or 96 h; and were then streaked across TYES medium. Bacteria were cultured from strips representing each drying interval, indicating that air-drying times of 96 h or less are insufficient to kill F. psychrophilum.

  17. Alloy 22 Localized Corrosion Susceptibility In Aqueous Solutions Of Chloride And Nitrate Salts Of Sodium And Potassium At 110 - 150?C

    SciTech Connect

    Felker, S; Hailey, P D; Lian, T; Staggs, K J; Gdowski, G E

    2006-01-17

    Alloy 22 (a nickel-chromium-molybdenum-tungsten alloy) is being investigated for use as the outer barrier of waste containers for a high-level nuclear waste repository in the thick unsaturated zone at Yucca Mountain, Nevada. Experiments were conducted to assess crevice corrosion of Alloy 22 in de-aerated aqueous solutions of chloride and nitrate salts of potassium and sodium in the temperature range 110-150 C (some limited testing was also conducted at 90 C). Electrochemical tests were run in neutral salt solutions without acid addition and others were run in salt solutions with an initial hydrogen ion concentration of 10{sup -4} molal. The Alloy 22 specimens were weld prism specimens and de-aeration was performed with nitrogen gas. No evidence of crevice corrosion was observed in the range 125-150 C. In the 120 to 160 C temperature range, the anionic concentration of stable aqueous solutions is dominated by nitrate relative to chloride. At nominally 120 C, the minimum nitrate to chloride ratio is about 4.5, and it increases to about 22 at nominally 155 C. The absence of localized corrosion susceptibility in these solutions is attributed to the known inhibiting effect of the nitrate anion. At 110 C, aqueous solutions can have dissolved chloride in excess of nitrate. Localized corrosion was observed at nitrate to chloride ratios up to 1.0, the highest ratio tested. The extent of localized corrosion was confined to the crevice region of the samples, and was limited for nitrate to chloride ratios greater than or equal to 0.3. Aqueous solution chemistry studies indicate that nitrate to chloride ratios of less than 0.5 are possible for temperatures up to nominally 116 C. However, the exact upper temperature limit is unknown and no electrochemical testing was done at these temperatures. Limited comparison between 8 m Cl aqueous solutions of Na + K on the one hand and Ca on the other indicated similar electrochemical E{sub crit} values and similar morphology of attack

  18. Viscometric study of chitosan solutions in acetic acid/sodium acetate and acetic acid/sodium chloride.

    PubMed

    Costa, Cristiane N; Teixeira, Viviane G; Delpech, Marcia C; Souza, Josefa Virginia S; Costa, Marcos A S

    2015-11-20

    A viscometric study was carried out at 25°C to assess the physical-chemical behavior in solution and the mean viscometric molar mass (M¯v) of chitosan solutions with different deacetylation degrees, in two solvent mixtures: medium 1-acetic acid 0.3mol/L and sodium acetate 0.2mol/L; and medium 2-acetic acid 0.1mol/L and sodium chloride 0.2mol/L. Different equations were employed, by graphical extrapolation, to calculate the intrinsic viscosities [η] and the viscometric constants, to reveal the solvent's quality: Huggins (H), Kraemer (K) and Schulz-Blaschke (SB). For single-point determination, the equations used were SB, Solomon-Ciuta (SC) and Deb-Chanterjee (DC), resulting in a faster form of analysis. The values of ̄M¯v were calculated by applying the equation of Mark-Houwink-Sakurada. The SB and SC equations were most suitable for single-point determination of [η] and ̄M¯v and the Schulz-Blachke constant (kSB), equal to 0.28, already utilized for various systems, can also be employed to analyze chitosan solutions under the conditions studied.

  19. Rheological characterization of solutions and thin films made from amylose-hexadecylammonium chloride inclusion complexes and polyvinyl alcohol.

    PubMed

    Hay, William T; Byars, Jeffrey A; Fanta, George F; Selling, Gordon W

    2017-04-01

    The rheological properties of aqueous solutions and films made from blends of polyvinyl alcohol (PVOH) and amylose-hexadecylammonium chloride inclusion complexes (Hex-Am) were investigated to better understand the polymer interactions and processing parameters. Aqueous solutions of Hex-Am displayed non-Newtonian shear thinning characteristics, becoming highly viscous at 4.2% solids and forming a strong mechanical gel at 10% solids. Cationic Hex-Am was observed to have dramatically different rheological temperature response profiles from anionic amylose-sodium palmitate inclusion complexes, displaying a precipitous increase in viscosity upon cooling from 95°C to 50°C. Aqueous solution blends of 1:1 PVOH/Hex-Am lack this precipitous increase in viscosity, indicating that PVOH reduces amylose-chain entanglement. Films cast from varying blends of Hex-Am and PVOH were thermostable to 200°C, and displayed decreasing storage modulus with increasing concentrations of PVOH in film blends. Films cast from Hex-Am/PVOH absorb water vapor at lower rates than their constitutive polymers.

  20. [Optimization of benzalkonium chloride concentration in 0.0015% tafluprost ophthalmic solution from the points of ocular surface safety and preservative efficacy].

    PubMed

    Asada, Hiroyuki; Takaoka-Shichijo, Yuko; Nakamura, Masatsugu; Kimura, Akio

    2010-06-01

    Optimization of benzalkonium chloride (alkyl dimethylbenzylammonium chloride: BAK) concentration as preservative in 0.0015% tafluprost ophthalmic solution (Tapros 0.0015% ophthalmic solution), an anti-glaucoma medicine, was examined from the points of ocular surface safety and preservative efficacy. BAKC(12), which is dodecyl dimethylbenzylammonium chloride, and BAKmix, which is the mixture of dodecyl, tetradecyl and hexadecyl dimethylbenzylammonium chloride were used in this study. The effects of BAKC(12) concentrations and the BAK types, BAKC(12) and BAKmix, in tafluprost ophthalmic solution on ocular surface safety were evaluated using the in vitro SV 40-immobilized human corneal epithelium cell line (HCE-T). Following treatments of Tafluprost ophthalmic solutions with BAKC(12), its concentration dependency was observed on cell viability of HCE-T. The cell viability of HCE-T after treatment of these solutions with 0.001% to 0.003% BAKC(12) for 5 minutes were the same level as that after treatment of the solution without BAK. Tafluprost ophthalmic solution with 0.01% BAKC(12) was safer for the ocular surface than the same solution with 0.01% BAKmix. Preservatives-effectiveness tests of tafluprost ophthalmic solutions with various concentrations of BAKC(12) were performed according to the Japanese Pharmacopoeia (JP), and solutions with more than 0.0005% BAKC(12) conformed to JP criteria. It was concluded that 0.0005% to 0.003% of BAKC(12) in tafluprost ophthalmic solution was optimal, namely, well-balanced from the points of ocular surface safety and preservative efficacy.

  1. Cardiovascular effects of hypertonic sodium chloride solutions when injected into the liquor space of anaesthetized cats.

    PubMed

    Feldberg, W; Wei, E

    1979-05-01

    1 In cats anaesthetized with chloralose, hyper- and hypotonic solutions were injected into the cisterna magna (in 0.5 ml) or into a lateral cerebral ventricle (in 0.2 to 0.3 ml), with aqueduct cannulated to prevent the injected solution from entering the subarachnoid space, and the effects on blood pressure and heart rate were examined. 2 Cisternal injections of hyper- and hypotonic solutions of NaCl (0.51 M and 0.05 M), glucose (1.03 M and 0.10 M), or sucrose (1.02 M and 0.10 M), as well as distilled water produced a rise in arterial blood pressure with tachycardias. Isotonic solutions of NaCl, glucose or sucrose were ineffective. 3 Ventricular injections of the hypertonic NaCl solution, also produced a pressor response with tachycardia effects when injected in this way. 4 The pressor responses and the tachycardias occurred after bilateral vagotomy and resulted from a sympathetic discharge which, on cisternal injection, originated from structures reached from the subarachnoid space, and on ventricular injection, from structures in the ventricular walls, probably in the hypothalamus. 5 The stimuli responsible for the discharge, were, on cisternal injection, the changes in osmolarity and on ventricular injection, the sodium ions.

  2. Evaluation of the cytotoxic effects of ophthalmic solutions containing benzalkonium chloride on corneal epithelium using an organotypic 3-D model

    PubMed Central

    Khoh-Reiter, Su; Jessen, Bart A

    2009-01-01

    Background Benzalkonium chloride (BAC) is a common preservative used in ophthalmic solutions. The aim of this study was to compare the cytotoxic effects of BAC-containing ophthalmic solutions with a BAC-free ophthalmic solution using an organotypic 3-dimensional (3-D) corneal epithelial model and to determine the effects of latanoprost ophthalmic solution and its BAC-containing vehicle on corneal thickness in a monkey model. Methods The cytotoxicity of commercially available BAC-containing ophthalmic formulations of latanoprost (0.02% BAC) and olopatadine (0.01% BAC) was compared to that of BAC-free travoprost and saline in a corneal organotypic 3-D model using incubation times of 10 and 25 minutes. To compare the extent of differentiation of 3-D corneal cultures to monolayer transformed human corneal epithelial (HCE-T) cell cultures, expression levels (mRNA and protein) of the corneal markers epidermal growth factor receptor, transglutaminase 1 and involucrin were quantified. Finally, latanoprost ophthalmic solution or its vehicle was administered at suprapharmacologic doses (two 30 μL drops twice daily in 1 eye for 1 year) in monkey eyes, and corneal pachymetry was performed at baseline and at weeks 4, 13, 26 and 52. Results In the 3-D corneal epithelial culture assays, there were no significant differences in cytotoxicity between the BAC-containing latanoprost and olopatadine ophthalmic solutions and BAC-free travoprost ophthalmic solution at either the 10- or 25-minute time points. The 3-D cultures expressed higher levels of corneal epithelial markers than the HCE-T monolayers, indicating a greater degree of differentiation. There were no significant differences between the corneal thickness of monkey eyes treated with latanoprost ophthalmic solution or its vehicle (both containing 0.02% BAC) and untreated eyes. Conclusion The lack of cytotoxicity demonstrated in 3-D corneal cultures and in monkey studies suggests that the levels of BAC contained in ophthalmic

  3. Differential elution of sodium or potassium dihydrogen- and hydrogenphosphate ions from a sephadex G-15 column with sodium or potassium chloride solution.

    PubMed

    Okada, T K; Miyakoshi, M; Inoue, M; Nakabayashi, Y; Jisaki, F

    2001-04-20

    When a mixed solution of sodium or potassium dihydrogenphosphate and disodium or dipotassium hydrogenphosphate was eluted from a Sephadex G-15 column with either a sodium or potassium chloride solution, the elution profiles of ions showed that the hydrogenphosphate ion was eluted more rapidly than the dihydrogenphosphate ion. When the sample solutions containing potassium dihydrogenphosphate and/or dipotassium hydrogenphosphate, all of which were supplemented with phosphorus-32-labelled potassium dihydrogenphosphate, were eluted with sodium chloride solution, the elution profiles of radioactivity showed that the dihydrogenphosphate ion changed to hydrogenphosphate ion and vice versa, depending on the pH values of the sample solution and the availability of the cation of the eluent during elution for the phosphate ion to pair with.

  4. Petrographic evidence of calcium oxychloride formation in mortars exposed to magnesium chloride solution

    SciTech Connect

    Sutter, Lawrence . E-mail: cee@mtu.edu; Peterson, Karl . E-mail: cee@mtu.edu; Touton, Sayward . E-mail: cee@mtu.edu; Van Dam, Tom . E-mail: cee@mtu.edu; Johnston, Dan . E-mail: Dan.Johnston@state.sd.us

    2006-08-15

    Many researchers have reported chemical interactions between CaCl{sub 2} and MgCl{sub 2} solutions and hardened Portland cement paste. One potentially destructive phase reported in the literature is calcium oxychloride (3CaO.CaCl{sub 2}.15H{sub 2}O). In the past, limited numbers of researchers have reported identification of this phase by X-ray diffraction. In this work, petrographic evidence of oxychloride formation is presented based on optical microscopy, scanning electron microscopy and microanalysis. This evidence indicates that calcium oxychloride does form in mortars exposed to MgCl{sub 2} solutions.

  5. Cooling and Freezing Behaviors of Aqueous Sodium Chloride Solution in a Closed Rectangular Container

    NASA Astrophysics Data System (ADS)

    Narumi, Akira; Kashiwagi, Takao; Nakane, Ichirou

    This paper investigates cooling and freezing behaviors of NaCl aqueous solution in a rectangular container equipped with horizontal partitions of micro porous film in order to determine the mechanisms of heat and mass transfer through cell wall for the purpose of freezing food. For comparison, experiments were performed using partitions of copper plate, no partition, and water. These processes were visualized and measured using real-time laser holographic interferometry. It was found that there was very little difference in the cooling process due to partitions, but that there were significant differences in freezing process when NaCl aqueous solution is used.

  6. Long-term cement-corrosion in chloride-rich solutions - a thermodynamic interpretation

    NASA Astrophysics Data System (ADS)

    Bube, C.; Metz, V.; Schild, D.; Bohnert, E.; Kienzler, B.

    2012-04-01

    Nuclear waste disposal relies on safe enclosure of radionuclides over long time-scales. Most experiments on interactions of radionuclides with barrier materials are running for several months, in some cases up to a few years. Very few experiments are available that confirm the results on longer time-scales and reassure that equilibrium conditions will be approached on the long term. This communication presents the latest results of full-scale cement corrosion experiments doped with uranium, which have been conducted for up to 22 years. Cemented waste simulates of 200L size were doped with Unat and exposed to MgCl2-rich or NaCl-saturated brine in the Asse salt mine (T = 28 ± 1 ° C). Solution composition and pH were monitored regularly. Some of the experiments were terminated in order to sample and analyze the solid phases. A geochemical code with a Pitzer database for high ionic strength systems is used to calculate the aqueous and solid phases expected at equilibrium conditions. In order to evaluate the thermodynamic database for the cementitious system, calculated solid phases and solution compositions were additionally compared to results of laboratory experiments on cement corrosion in MgCl2-rich solutions with mass to volume ratios (m/V) between 0.025 and 1.0. Solid and solution composition of the laboratory experiments after ~3 years agree well with results predicted from the thermodynamic calculations. With increasing m/V, transformation of the initial MgCl2-rich solutions into CaCl2-rich solutions is observed. This exchange reaction of Mg from the solution against Ca in the cement leads to a pHm (-log[H+]) increase up to 12 (from initial values around 9). Major solid phases found by analytical methods are also obtained in the calculations (e.g. gypsum, calcite, hydrotalcite / friedel's salt, brucite). Discrepancies are caused by various amorphous phases, which cannot be represented in the database. In the full-scale experiments (with m/V around 2.7), a

  7. Aqueous combustion synthesis of aluminum oxide thin films and application as gate dielectric in GZTO solution-based TFTs.

    PubMed

    Branquinho, Rita; Salgueiro, Daniela; Santos, Lídia; Barquinha, Pedro; Pereira, Luís; Martins, Rodrigo; Fortunato, Elvira

    2014-11-26

    Solution processing has been recently considered as an option when trying to reduce the costs associated with deposition under vacuum. In this context, most of the research efforts have been centered in the development of the semiconductors processes nevertheless the development of the most suitable dielectrics for oxide based transistors is as relevant as the semiconductor layer itself. In this work we explore the solution combustion synthesis and report on a completely new and green route for the preparation of amorphous aluminum oxide thin films; introducing water as solvent. Optimized dielectric layers were obtained for a water based precursor solution with 0.1 M concentration and demonstrated high capacitance, 625 nF cm(-2) at 10 kHz, and a permittivity of 7.1. These thin films were successfully applied as gate dielectric in solution processed gallium-zinc-tin oxide (GZTO) thin film transistors (TFTs) yielding good electrical performance such as subthreshold slope of about 0.3 V dec(-1) and mobility above 1.3 cm2 V(-1) s(-1).

  8. Thermophysical properties of sodium nitrate and sodium chloride solutions and their effects on fluid flow in unsaturated media

    SciTech Connect

    Xu, Tianfu; Pruess, Karsten

    2001-10-01

    Understanding movement of saline sodium nitrate (NaNO{sub 3}) waste solutions is important for assessing the contaminant migration near leaking waste storage tanks in the unsaturated zone at the Hanford site (Washington, USA). The purpose of this study is to contribute a basic understanding of effects of the thermophysical behavior of NaNO{sub 3} solutions on fluid flow in unsaturated media. We first present mathematical expressions for the dependence of density, viscosity, solubility and vapor pressure of NaNO{sub 3} solutions on both salt concentration and temperature, which were determined by fitting from published measured data. Because the previous studies of thermophysical behavior of sodium chloride (NaCl) solutions can provide a basis for those of NaNO{sub 3} solutions, we also present a comparison of thermophysical properties of both salt solutions. We have implemented the functional thermophysical properties of NaNO{sub 3} solutions into a new TOUGH2 equation-of-state module EWASG-NaNO{sub 3}, which is modified from a previous TOUGH2 equation-of-state module EWASG for NaCl. Using the simulation tool, we have investigated effects of the thermophysical properties on fluid flow in unsaturated media. The effect of density and viscosity of saline solutions has been long recognized. Here we focus our attention on the effect of vapor pressure lowering due to salinity. We present simulations of a one-dimensional problem to study this salinity-driven fluid flow. A number of simulations were performed using different values of thermal conductivity, permeability, and temperature, to illustrate conditions and parameters controlling these processes. Results indicate that heat conduction plays a very important role in this salinity-driven vapor diffusion by maintaining a nearly constant temperature. The smaller the permeability, the more water is transferred into the saline environment. Effects of permeability on water flow are also complicated by effects of capillary

  9. [Adsorption Characteristics of Nitrate and Phosphate from Aqueous Solution on Zirconium-Hexadecyltrimethylammonium Chloride Modified Activated Carbon].

    PubMed

    Zheng, Wen-jing; Lin, Jian-wei; Zhan, Yan-hui; Wang, Hong

    2015-06-01

    A novel adsorbent material, i.e., zirconium-cationic surfactant modified activated carbon (ZrSMAC) was prepared by loading zirconium hydroxide and hexadecyltrimethylammonium chloride (CTAC) on activated carbon, and was used as an adsorbent for nitrate and phosphate removal from aqueous solution. The adsorption characteristics of nitrate and phosphate on ZrSMAC from aqueous solution were investigated in batch mode. Results showed that the ZrSMAC was effective for nitrate and phosphate removal from aqueous solution. The pseudo-second-order kinetic model fitted both the nitrate and phosphate kinetic experimental data well. The equilibrium isotherm data of nitrate adsorption onto the ZrSMAC were well fitted to the Langmuir, Dubinin-Radushkevich (D-R) and Freundlich isotherm models. The equilibrium isotherm data of phosphate adsorption onto the ZrSMAC could be described by the Langmuir and,D- R isotherm models. According to the Langmuir isotherm model, the maximum nitrate and phosphate adsorption capacities for the ZrSMAC were 7.58 mg x g(-1) and 10.9 mg x g(-1), respectively. High pH value was unfavorable for nitrate and phosphate adsorption onto the ZrSMAC. The presence of Cl-, HCO3- and SO4(2-) in solution reduced the nitrate and phosphate adsorption capacities for the ZrSMAC. The nitrate adsorption capacity for the ZrSMAC was reduced by the presence of coexisting phosphate in solution, and the phosphate adsorption capacity for the ZrSMAC was also reduced by the presence of coexisting nitrate in solution. About 90% of nitrate adsorbed on the ZrSMAC could be desorbed in 1 mol x L(-1) NaCl solution, and about 78% of phosphate adsorbed on the ZrSMAC could be desorbed in 1 mol x L(-1) NaOH solution. The adsorption mechanism of nitrate on the ZrSMAC included the anion exchange interactions and electrostatic attraction, and the adsorption mechanism of phosphate on the ZrSMAC included the ligand exchange interaction, electrostatic attraction and anion exchange interaction.

  10. Hydrometallurgical extraction of zinc from CaO treated EAF dust in ammonium chloride solution.

    PubMed

    Miki, Takahiro; Chairaksa-Fujimoto, Romchat; Maruyama, Katsuya; Nagasaka, Tetsuya

    2016-01-25

    Zinc in Electric Arc Furnace dust or EAF dust mainly exists as ZnFe2O4 and ZnO. While ZnO can be simply dissolved into either an acidic or alkaline solution, it is difficult to dissolve ZnFe2O4. In our previous work, we introduced a process called "CaO treatment", a preliminary pyrometallurgical process designed to transform the ZnFe2O4 in the EAF dust into ZnO and Ca2Fe2O5. The halogens and others heavy metals were favorably vaporized during CaO treatment with no essential evaporation loss of zinc and iron, leaving CaO treated dust which consisted mainly of ZnO and Ca2Fe2O5 and no problematic ZnFe2O4 compound. In this work, the selective leaching of zinc over iron and calcium in the CaO treated dust was investigated using an NH4Cl solution. The effects of temperature, reaction time and NH4Cl concentration on dissolution behavior were examined. While most of the zinc in the CaO treated dust was extracted after 2 h at 70 °C with 2 M NH4Cl, only about 20% of calcium was leached in NH4Cl solution. However, the iron did not dissolve and remained as Ca2Fe2O5 in residue. It was confirmed that zinc can be effectively recovered using NH4Cl solution.

  11. Sodium chloride crystallization from drying drops of albumin-salt solutions with different albumin concentrations

    NASA Astrophysics Data System (ADS)

    Yakhno, T. A.

    2015-11-01

    The salt nature of crystalline structures resulting from drying albumin-salt solutions with a low (<1 wt %) and high (7 and 9 wt %) concentration of albumin and a NaCl concentration kept at a physiological level (0.9 wt %) is experimentally substantiated. Such a conclusion is drawn from the dynamics of phase transitions, morphological studies, and differences between the physicochemical properties of albumin and salt. Obtained data give a deeper insight into the albumin and salt distributions in drying liquids.

  12. The Interaction of Polycrystalline Copper Films with Dilute Aqueous Solutions of Cupric Chloride

    DTIC Science & Technology

    1989-10-01

    in atmosphere has always been of interest because of the extensive use of copper and brass in buildings and statues, for example. A study by Pinnel et...solution and the sample surface layer have been reported with no mention of the microstructure of the copper sample except for a few cases where chemical...used as a substrate when the deposited film will be removed for mechanical testing. In this case , the copper film was removed prior to characterization

  13. Hydrolysis equilibria of tungsten(VI) in aqueous sodium chloride solutions to 300/sup 0/C

    SciTech Connect

    Wesolowski, D.; Drummond, S.E.; Mesmer, R.E.; Ohmoto, H.

    1984-04-11

    Formation constants for the protonated mononuclear and polynuclear forms of tungstate have been measured by means of a hydrogen electrode concentration cell from 95 to 290/sup 0/C in 0.10-5.1 m NaCl solutions over a pH range of 2-8 and tungsten concentration from 5 X 10/sup -4/ to 10/sup -2/m. Polytungstates dominate the speciation in the 10/sup -2/ m solutions below a pH of 5, particularly in the low-temperature solutions. Monomers become increasingly stable at low tungsten concentrations, high temperatures, and high ionic strengths and are the only form of tungsten detected above 200/sup 0/C at 5.1 m NaCl. The equilibrium quotients for the reaction WO/sub 4//sup 2-/ + H/sup +/ reverse arrow..-->..HWO/sub 4//sup -/ have been determined to 300/sup 0/C over the entire composition range. An analytical expression for the temperature and ionic strength dependence of these equilibrium quotients and derived thermodynamic properties are presented.

  14. Two-Stage Separation of V(IV) and Al(III) by Crystallization and Solvent Extraction from Aluminum-Rich Sulfuric Acid Leaching Solution of Stone Coal

    NASA Astrophysics Data System (ADS)

    Shi, Qihua; Zhang, Yimin; Liu, Tao; Huang, Jing; Liu, Hong

    2016-12-01

    To improve separation of V(IV) and Al(III) from aluminum-rich sulfuric acid leaching solution of stone coal, the two-stage separation by crystallization and solvent extraction methods have been developed. A co-extraction coefficient (k) was put forward to evaluate comprehensively co-extraction extent in different solutions. In the crystallization stage, 68.2% of aluminum can be removed from the solution. In the solvent extraction stage, vanadium was selectively extracted using di-2-ethylhexyl phosphoric acid/tri-n-butyl phosphate from the crystalline mother solution, followed by H2SO4 stripped efficiently. A V2O5 product with purity of 98.39% and only 0.10% Al was obtained after oxidation, precipitation, and calcination. Compared with vanadium extraction from solution without crystallization, the counter-current extraction stage of vanadium can be decreased from 6 to 3 and co-extraction coefficient (k) decreased from 2.51 to 0.58 with two-stage separation. It is suggested that the aluminum removal by crystallization can evidently weaken the influence of aluminum co-extraction on vanadium extraction and improve the selectivity of solvent extraction for vanadium.

  15. The role of the binding salt sodium salicylate in semidilute ionic cetylpyridinium chloride micellar solutions: a rheological and scattering study.

    PubMed

    Gaudino, D; Pasquino, R; Stellbrink, J; Szekely, N; Krutyeva, M; Radulescu, A; Pyckhout-Hintzen, W; Grizzuti, N

    2016-12-21

    The micellar system based on cetylpyridinium chloride (CPyCl) and sodium salicylate (NaSal) in brine solution is investigated on both macro- and micro-length scales through rheology and scattering measurements. The linear viscoelasticity of the system and its structural parameters are explored by systematically changing the amount of NaSal over an extremely wide range of concentrations, thus producing salt-to-surfactant molar ratios from zero to about 8.5. As a result, the well-known non-monotonic behaviour of the zero-shear rate viscosity as a function of salinity can be connected to micellar morphological changes, whose driving force is represented by the simultaneous binding and screening actions of NaSal. The viscosity behaviour can be seen as a direct consequence of consecutive lengthening/shortening of the contour length, where the micelles attempt to minimize the electrostatic charge density on their surface. Along similar lines, the scattering measurements of the semidilute solutions show that the local stiffness of the micellar chain changes with increasing salt content influencing the elasticity of the resulting network. Within this general view, the branching of the micelles can be seen as a side effect attributable to the main character of the play, namely, the binding salt NaSal, whereas the overall dynamics of the system is driven by the considerable changes in the entanglement density of the micellar network.

  16. Study of benzotriazole as corrosion inhibitors of carbon steel in chloride solution containing hydrogen sulfide using electrochemical impedance spectroscopy (EIS)

    SciTech Connect

    Solehudin, Agus; Nurdin, Isdiriayani

    2014-03-24

    Corrosion and inhibition studies on API 5LX65 carbon steel in chloride solution containing various concentrations of benzotriazole has been conducted at temperature of 70°C using Electrochemical Impedance Spectroscopy (EIS). Corroded carbon steel surface with and without inhibitor have been observed using X-ray Diffraction (XRD), Scanning Electron Microscope (SEM), and Energy Dispersive Spectroscopy (EDS). The objectives of this research are to study the performance of benzotriazole as corrosion inhibitors. The experimental results of carbon steel corrosion in 3.5% NaCl solution containing 500 mg/l H{sub 2}S at different BTAH concentrations showed that corrosion rate of carbon steel decreases with increasing of BTAH concentrations from 0 to 10 mmol/l. The inhibition efficiency of BTAH was found to be affected by its concentration. The optimum efficiency obtained of BTAH is 93% at concentration of 5 mmol/l. The result of XRD and EDS analysis reveal the iron sulfide (FeS) formation on corroded carbon steel surface without inhibitor. The EDS spectrum show the Nitrogen (N) bond on carbon steel surface inhibited by BTAH.

  17. An experimental determination of ferrous chloride and acetate complexation in aqueous solutions to 300°C

    NASA Astrophysics Data System (ADS)

    Palmer, Donald A.; Hyde, K. E.

    1993-04-01

    The formation of the monochloroiron(II) complex, FeCl +, was studied potentiometrically from 125 to 295°C at 25 degree intervals at one molal ionic strength in aqueous solutions containing acetic acid, sodium acetate, and sodium trifluoromethanesulfonate. In this method, competition between chloride and acetate ions for the ferrous cation resulted in a change in solution pH, which in turn was monitored in situ in a hydrogen-electrode, concentration cell. A simple empirical approach was used to extrapolate these formation quotients to infinite dilution. The resulting constants proved to be in excellent agreement with previous spectrophotometric results obtained from 25 to 200°C. Thus, the present study confirms the validity of the conclusions made based on these earlier data concerning the solubility of Fe-containing minerals in hydrothermal brines. Formation constants at infinite dilution for FeCl + are compared with the stability of ferrous acetate and hydroxide complexes. The original potentiometric titration data for ferrous acetate complex formation were combined in a new fit with values determined from the present study at unit ionic strength. Two empirical treatments (namely the isocoulombic method and the temperature/water density function) were considered for fitting and extrapolating the infinite dilution formation constants to 350°C.

  18. Parenteral drug products containing aluminum as an ingredient or a contaminant: Response to Food and Drug Administration notice of intent and request for information. ASCN/A. S. P. E. N. Working Group on Standards for Aluminum Content of Parenteral Nutrition Solutions

    SciTech Connect

    Not Available

    1991-03-01

    Aluminum remains a significant contaminant of total parenteral nutrition (TPN) solutions and may be elevated in bone, urine, and plasma of infants receiving TPN. Aluminum accumulation in tissues of uremic patients and adult TPN patients has been associated with low-turnover bone disease. Furthermore, aluminum has also been linked with encephalopathy and anemia in uremic patients and with hepatic cholestasis in experimental animals. Because of the toxic effects of aluminum, the Food and Drug Administration (FDA) recently published a notice of intent to set an upper limit of 25 micrograms/L for aluminum in large-volume parenterals and to require manufacturers of small-volume parenterals, such as calcium and phosphate salts, to measure aluminum content and note this content on the package label. The ASCN/A.S.P.E.N. Working Group on Standards for Aluminum Content of Parenteral Nutrition Solutions supports these intentions and further urges the FDA to require that cumulative aluminum intake in terms of safe, unsafe, and toxic quantities of aluminum per kilogram be made known to physicians and pharmacists preparing the TPN solutions, to ensure that manufacturers use appropriate control procedures in aluminum measurements, and to employ a standard unit of aluminum measurement.

  19. A comparative study on the electrochemical corrosion behavior of iron and X-65 steel in 4.0 wt % sodium chloride solution after different exposure intervals.

    PubMed

    Sherif, El-Sayed M

    2014-07-09

    In this work, the results obtained from studying the anodic dissolution of pure iron and API X-65 5L pipeline steel after 40 min and 12 h exposure period in 4.0 wt % NaCl solutions at room temperature were reported. Potential-time, electrochemical impedance spectroscopy, potentiodynamic polarization, and chronoamperometric current-time at constant potential techniques were employed. It has been found that the iron electrode corrodes in the chloride test solutions faster than the API X-65 5L steel does under the same conditions. Increasing the exposure period for the electrodes from 40 min to 12 h showed a significant reduction in the corrosion parameters for both iron and steel in the 4.0 wt % NaCl solution. Results together confirmed clearly that the X-65 steel is superior to iron against corrosion in sodium chloride solutions.

  20. Inefficacy of osmotic backwash induced by sodium chloride salt solution in controlling SWRO membrane fouling

    NASA Astrophysics Data System (ADS)

    Farooque, A. Mohammed; Al-Jeshi, Subhi; Saeed, Mohamed O.; Alreweli, Ali

    2014-12-01

    A study was conducted to evaluate the efficacy of osmotic backwash induced by high salt (NaCl) concentration solution on feed side of seawater reverse osmosis (SWRO) membranes, online and offline, in controlling membrane fouling and therefore minimizing/eliminating the need for chemical cleaning. SWRO membranes were deliberately fouled by feeding seawater from an open intake located on the Arabian Gulf Coast without dosing chemicals. The fouled membranes were subjected to offline cleaning with the salt solution of up to 25 % concentration. Despite the partial removal of foulants from the membrane surface, SWRO membrane performance could not be restored, indicating the ineffectiveness of osmotic backwash in aiding offline salt cleaning. Similarly, online osmotic backwash was found to be not only ineffective in removing foulants from membrane surfaces but actually increased the fouling rate, as indicated by faster fouling rates compared to other cases. Although the driving force required for the osmotic backwash existed, the generated back flow proved to be insufficient to detach foulants from membrane surfaces. During the study period, the average SWRO membrane flux was maintained between 19 and 23 LMH, whereas the average generated back flow flux by high salt concentration solution was only 11 LMH, which was not adequate to remove foulants from membrane surfaces. Moreover, it seems that the membrane configuration as well as inherent microstructure of SWRO membrane places certain constraints on the osmotic backwash process and renders osmotic backwash ineffective in tackling SWRO membrane fouling. Hence, chemical cleaning is essential to restore SWRO membrane performance whenever fouling occurs, and the use of highly concentrated salt solution does not have any significant benefit. Membrane autopsy revealed only an insignificant accumulation of biofouling layer despite the absence of disinfection. However, it was shown that culturable biofilm bacteria species

  1. Correlations between structure, spectra, and thermodynamics in solutions of cobalt chloride in sodium tetrachloroaluminates

    SciTech Connect

    Newman, D.S.; Tumidajski, P.J.; Blander, M.

    1990-01-01

    An EMF technique using the cell Co/CoCl{sub 2} {minus} Na AlCl{sub 4}//(AgCl)x {minus} NaAlCl{sub 4} (x fixed)/Ag was used to measure the solubility of CoCl{sub 2} in NaCl{center dot}AlCl{sub 3} melts. The changes in EMF as a function of changes in melt composition were correlated with changes in the UV-Vis spectra of the dissolved cobalt species. From these data the microscopic structural contributions to the macroscopic thermodynamic properties of the solutions were estimated. 14 refs., 5 figs., 1 tab.

  2. Corrosion Fatigue Behavior of 316LN SS in Acidified Sodium Chloride Solution at Applied Potential

    NASA Astrophysics Data System (ADS)

    Poonguzhali, A.; Pujar, M. G.; Mallika, C.; Mudali, U. Kamachi

    2015-05-01

    The influence of acidified 1 M NaCl solution by addition of 2 ml/L of HCl on the cyclic plastic deformation of AISI Type 316LN SS containing 0.07 wt.% and 0.22 wt.% N was investigated as a function of the applied potentials. The corrosion fatigue (CF) behavior of stainless steel (SS) was explained vis-a-vis the dislocation behavior, the propensity to form microcracks, and the evolution of the current transients based on the studies carried out at both room-temperature and boiling conditions. CF experiments were conducted using round tensile specimens at a stress ratio of 0.5 and a frequency of 0.1 Hz. Two different kinds of damage mechanisms were observed (I) the damage mechanism in the stable-passive state was correlated with the localization of the anodic dissolution due to a depassivation-repassivation process, whereas (II) the cyclic stress induced pitting corrosion in the metastable pitting state, which resulted in formation of microcracks. The study of the microcracking process and its evolution is a key to the physical mechanism by which the fatigue life of stainless steels would be affected in an aqueous corrosive solution under the applied potential.

  3. Corrosion Behavior of Stainless Steels in Neutral and Acidified Sodium Chloride Solutions by Electrochemical Impedance Spectroscopy

    NASA Technical Reports Server (NTRS)

    Calle, L. M.; Kolady, M. R.; Vinje, R. D.

    2004-01-01

    The objective of this work was to evaluate the corrosion performance of three alloys by Electrochemical Impedance Spectroscopy (EIS) and to compare the results with those obtained during a two-year atmospheric exposure study.' Three alloys: AL6XN (UNS N08367), 254SM0 (UNS S32154), and 304L (UNS S30403) were included in the study. 304L was included as a control. The alloys were tested in three electrolyte solutions which consisted of neutral 3.55% NaC1, 3.55% NaC1 in 0.lN HC1, and 3.55% NaC1 in 1.ON HC1. These conditions were expected to be less severe, similar, and more severe respectively than the conditions at NASA's Kennedy Space Center launch pads.

  4. Separation of mercury from aqueous mercuric chloride solutions by onion skins

    SciTech Connect

    Asai, S.; Konishi, Y.; Tomisaki, H.; Nakanishi, M.

    1986-01-01

    The separation of mercury from aqueous HgCl/sub 2/ solutions by onion skins (outermost coat) was studied both experimentally and theoretically. The distribution equilibria were measured by the batchwise method. The experimental results revealed that onion skin is a useful material for separating mercury from aqueous systems. The distribution data obtained at 25/sup 0/C were analyzed by using the theory based on the law of mass action. The separation of dissolved mercury by onion skins was found to be a process accompanied by an ion-exchange reaction of the cationic complex HgCl/sup +/ and an adsorption of the neutral complex HgCl/sub 2/. The equilibrium constants of the ion-exchange and adsorption processes at 25/sup 0/C and the mercury-binding capacity of onion skins were determined. Further, it was found that the distribution equilibrium of mercury is comparatively insensitive to temperature.

  5. Determination of benzalkonium chloride in ophthalmic solutions containing tyloxapol by solid-phase extraction and reversed-phase high-performance liquid chromatography.

    PubMed

    Fan, T Y; Wall, G M

    1993-11-01

    A procedure using solid-phase extraction (Supelcoclean CN) followed by HPLC [Beckman Ultrasphere CN, acetonitrile:phosphate solution (60:40, v/v)] was developed and validated to quantitate the quaternary ammonium preservative benzalkonium chloride in an experimental ophthalmic formulation containing the polymeric material tyloxapol. This procedure makes routine determinations of benzalkonium chloride at concentrations of 0.0035 to 0.01% simpler than the traditional ion-pairing colorimetric methods. This method is quick, specific, and especially useful for drug product stability studies. In addition, because the method distinguishes each homologue, it can be extended to routinely determine the homologue ratio for quality control purposes.

  6. Electrochemical chloride extraction: efficiency and side effects

    SciTech Connect

    Orellan, J.C.; Escadeillas, G.; Arliguie, G

    2004-02-01

    Some specimens of reinforced concrete cast with an alkali-resistant aggregate, previously maintained in a solution of NaCl, were subjected to an electrochemical chloride extraction (ECE). The chloride profiles before and after treatment were determined. Likewise, alkali ions profiles before and after treatment were determined. After treatment, some specimens were stored in a controlled atmosphere (60 deg. C and 100% RH) in order to accelerate the alkali-silica reaction, if any. Results of chloride content after treatment show that about 40% of the initial chloride is removed within 7 weeks. About one-half of the chloride close to steel was removed, but at the same time, significant amounts of alkali ions were observed around the steel. Microstructural observations by scanning electron microscopy (SEM) showed that after treatment, new cementitious phases containing higher concentrations of sodium, aluminum and potassium were formed. Moreover, alkali-silica gel was observed in the specimens stored at 60 deg. C and 100% RH. It may be possible that the ECE accumulates locally high amounts of alkali ions that stimulate the alkali-silica reaction even though the concrete contained nominally inert siliceous aggregates. The specimen expansions were not recorded, but no cracks were observed.

  7. Structural characterization of zinc(II) chloride in aqueous solution and in the protic ionic liquid ethyl ammonium nitrate by x-ray absorption spectroscopy.

    PubMed

    D'Angelo, Paola; Zitolo, Andrea; Ceccacci, Francesca; Caminiti, Ruggero; Aquilanti, Giuliana

    2011-10-21

    Extended x-ray absorption fine structure (EXAFS) spectroscopy has been used to investigate the species and structures existing in a series of ZnCl(2)-H(2)O-NaCl solutions with different chloride/zinc ratios and in a solution of ZnCl(2) in the protic ionic liquid ethyl ammonium nitrate (EAN). The average coordination numbers and distances of zinc species were determined from the analysis of the EXAFS data. In aqueous solution the number of chloride ions tightly bounded to Zn(2+) is significantly related to the chloride/zinc ratio, and no inner complex formation between Zn(2+) and Cl(-) ions has been detected for low ZnCl(2) concentration (0.1 and 0.2 M). Conversely, in the same concentration range (0.13 M) the ZnCl(2) species do not dissociate in EAN and the Zn(2+) first coordination shell has two chloride ions and is completed by two oxygen atoms of the nitrate anion. The results of this investigation show that notwithstanding the existence of similar characteristics between EAN and water, the solvation properties of the two solvents are markedly different.

  8. Environmentally Assisted Cracking of Alloy 7050-T7451 Exposed to Aqueous Chloride Solutions

    NASA Astrophysics Data System (ADS)

    Braun, Reinhold

    2016-03-01

    The stress corrosion cracking (SCC) behavior of 7050-T7451 plate material was investigated in short-transverse direction performing constant load and constant extension rate tests. Smooth and notched tensile specimens were permanently immersed in substitute ocean water and in an aqueous solution of 0.6 M NaCl + 0.06 M (NH4)2SO4. Alloy 7050-T7451 exhibited high SCC resistance in both synthetic environments. However, conducting cyclic loading tests, environment-induced cracking was observed. Applying a sawtooth waveform, notched tensile specimens were strained under constant load amplitude conditions at constant displacement rates ranging from 2 × 10-6 to 2 × 10-4 mms-1. The stress ratio R = σ min/ σ max was 0.1 with maximum stresses of 300 and 400 MPa. When cyclically loaded in substitute ocean water, notched specimens failed predominantly by transgranular environment-induced cracking. Striations were observed on the cleavage-like facets. The number of cycles-to-failure decreased with decreasing displacement rate. A slope of 0.5 was obtained by fitting the logarithmic plot of number of cycles-to-failure vs nominal loading frequency, indicating a hydrogen embrittlement mechanism controlled by diffusion.

  9. CO sub 2 induced inhibition of the localized corrosion of aluminum, Al-0. 5% Cu, and Al-2% Cu in dilute HF solution

    SciTech Connect

    Scully, J.R. . Dept. of Materials Science); Peebles, D.E. )

    1991-01-01

    This study presents work on corrosion of aluminum, Al-.5% Cu, and Al-2% Cu. Electrochemical tests were performed in dilute HF solutions both with and without CO{sub 2} sparging. It is suggested that CO{sub 2} or its reaction products interact with the passive film so that exposure of Cu in the oxide-solution interface is minimized. CO{sub 2} is investigated as a corrosion inhibitor. 4 refs. (JDL)

  10. Bioactivity of porous titanium with hydrogen peroxide solution with or without tantalum chloride treatment at a low temperature.

    PubMed

    Zhao, Chaoyong; Liang, Kailu; Tan, Jing; Xiang, Zhou; Fan, Hongsong; Zhang, Xingdong

    2013-04-01

    In this study, porous titanium was treated by a hydrogen peroxide solution with (HT) or without (HO) tantalum chloride at a low temperature to endow its bioactivity. The microstructure, film stability and in vitro and in vivo bioactivity of HT-treated and HO-treated porous titanium were investigated, and the non-treated one was used as control. After HT treatment, a well-crystallized titania nanoparticle film consisting of anatase phase with good film stability was formed on the surface of porous titanium, and the tantalum element appeared in the film, while the HO-treated porous titanium surface showed a dual structure with well-aligned nanorods as an outer layer and condensed nanoparticles as an inner layer consisting of a mixture of well-crystallized anatase and rutile phases. In vitro bioactivity assessment showed that both HT- and HO-treated porous titanium possessed high apatite-forming ability. More importantly, after implantation in the dorsal muscles of dogs, the HT- and HO-treated implants induced ectopic bone formation in its inner pores after 5 months, while the non-treated one did not. The present study showed that HT-treated porous titanium possessed good film stability and bioactivity to be used as bone repair materials in clinic under load-bearing conditions.

  11. A new dioxime corrosion inhibitor for the protection and conservation of copper: synthesis, characterization and evaluation in acidic chloride solution

    NASA Astrophysics Data System (ADS)

    Abu-Baker, Ahmad N.; Al-Qudah, Mahmoud A.

    2016-08-01

    This study aimed to investigate a new dioxime compound as a corrosion inhibitor for copper. The compound (4,6-dihydroxy benzene-1,3-dicarbaldehyde dioxime) was synthesized and characterized by nuclear magnetic resonance spectroscopy. Electrochemical impedance spectroscopy and potentiodynamic polarization measurements were used to compare the dioxime compound with benzotriazole for their effectiveness as corrosion inhibitors for copper in 0.1 M HCl solution. Fourier transform infrared (FTIR) spectroscopy and scanning electron microscopy (SEM) were used to investigate the bonding mechanisms and morphological changes of the two inhibitors on the copper surface. The electrochemical techniques showed that the new dioxime compound was more effective than benzotriazole in inhibiting copper corrosion in the acidic chloride medium. The FTIR and SEM results indicated that the dioxime compound was able to coordinate with copper ions and formed a protective film on the copper surface. It was concluded that the new dioxime compound proved effectiveness to be used as a corrosion inhibitor for the protection and conservation of copper.

  12. An investigation into the use of cuprous chloride for the removal of radioactive iodide from aqueous solutions.

    PubMed

    Liu, Yang; Gu, Ping; Jia, Lin; Zhang, Guanghui

    2016-01-25

    Cuprous chloride (CuCl) was examined as a precipitant to remove iodide (I(-)) from aqueous solutions. The effects of the dosage of CuCl, reaction time, initial concentrations of I(-) and bicarbonate (HCO3(-)) on I(-) removal were investigated. The results showed that the optimized removal efficiency of I(-) reached approximately 95.8% when the dosage was 150 mg/L, the initial I(-) concentration ranged from 5 to 40 mg/L and the reaction time was 15 min. The removal efficiency decreased from 95.8% to 76.0% with the addition of HCO3(-) at a concentration in the range of 0-107 mg/L. Furthermore, the dissociation of CuCl, the disproportionation reaction of Cu(+), the precipitation of cuprous iodide (CuI) and cuprous oxide (Cu2O), and the formations of copper sulfide (CuxS, 1≤x<2) were identified as the primary reactions using the PHREEQC software and the measurements of water quality parameters under various conditions. X-rays photoelectron spectroscopy (XPS) analysis was performed before and after the reaction, helping to elucidate the reaction mechanism. This study can provide a promising method to address radioactive I(-) pollution in water.

  13. Influence of the current density on the electrochemical treatment of concentrated 1-butyl-3-methylimidazolium chloride solutions on diamond electrodes.

    PubMed

    Marcionilio, Suzana M L de Oliveira; Alves, Gisele M; E Silva, Rachel B Góes; Marques, Pablo J Lima; Maia, Poliana D; Neto, Brenno A D; Linares, José J

    2016-10-01

    This paper focuses on the influence of the current density treatment of a concentrated 1-butyl-3-methylimidazolium chloride (BMImCl) solution on an electrochemical reactor with a boron-doped diamond (BDD) anode. The decrease in the total organic carbon (TOC) and the BMImCl concentration demonstrate the capability of BDD in oxidizing ionic liquids (ILs) and further mineralizing (to CO2 and NO3 (-)) more rapidly at higher current densities in spite of the reduced current efficiency of the process. Moreover, the presence of Cl(-) led to the formation of oxychlorinated anions (mostly ClO3 (-) and ClO4 (-)) and, in combination with the ammonia generated in the cathode from the nitrate reduction, chloramines, more intensely at higher current density. Finally, the analysis of the intermediates formed revealed no apparent influence of the current density on the BMImCl degradation mechanism. The current density presents therefore a complex influence on the IL treatment process that is discussed throughout this paper.

  14. Removal of malachite green dye from aqueous solution using mesoporous silica synthesized from 1-octyl-3-methylimidazolium chloride ionic liquid

    NASA Astrophysics Data System (ADS)

    Ekka, Basanti; Nayak, Soumitra Ranjan; Dash, Priyabrat; Patel, Raj Kishore

    2016-04-01

    In this research, mesoporous silica was synthesized via a modified sol-gel route using 1-octyl-3-methylimidazolium chloride and was employed to remove malachite green (MG) dye from aqueous solution. Subsequently, this material was characterized and identified by different techniques such as Fourier transform infrared spectroscopy (FT-IR), N2 adsorption-desorption method, scanning electron microscopy (SEM), and thermosgravimetric analysis (TGA). Unique properties such as high surface area and pore diameter, in addition to highly reactive atoms and presence of various functional groups make the mesoporous silica possible for efficient removal of malachite green (MG). In batch experimental set-up, optimum conditions for quantitative removal of MG by mesoporous silica was attained by varying different variables such as adsorbent dosage, initial dye concentration, contact time, and pH. Optimum values were set as pH of 8.0, 0.5 g of adsorbent at contact time of 120 min. The adsorption of MG follows the pseudo-second-order rate equation. Equilibrium data fitted well with the Freundlich model at all amount of adsorbent, while maximum adsorption capacity was 5.981 mg g-1 for 0.5 g mesoporous silica synthesized in IL.

  15. Treatment of Basic Red 29 dye solution using iron-aluminum electrode pairs by electrocoagulation and electro-Fenton methods.

    PubMed

    Yavuz, Yusuf; Shahbazi, Reza; Koparal, A Savaş; Öğütveren, Ulker Bakır

    2014-01-01

    The aim of this study is the treatment of Basic Red 29 (BR29) dye solution using hybrid iron-aluminum electrodes by electrocoagulation and electro-Fenton methods. The effect of current density, initial pH, supporting electrolyte, H₂O₂, and initial dye concentration on dye removal efficiency was investigated, and the best experimental conditions were obtained. Time-coarse variation of UV-Vis spectra and toxicity and chemical oxygen demand (COD) removal were also examined at the best experimental conditions. Both systems were found very successful for the removal of BR29 dye. The removal efficiency of >95% for BR29 dye solution was reached easily in a short time. At the best experimental conditions, for the initial BR29 concentration of 100 mg/L, >95% BR29 dye and 71.43% COD removal were obtained after 20 and 40 min of electrolysis, respectively. Additionally, toxicity results for electro-Fenton treatment of 100 mg/L BR29 were also very promising. According to the results obtained, although electro-Fenton is more effective, both systems can be used successfully to treat textile wastewater including dyes.

  16. Reactive solute transport in an acidic stream: Experimental pH increase and simulation of controls on pH, aluminum, and iron

    USGS Publications Warehouse

    Broshears, R.E.; Runkel, R.L.; Kimball, B.A.; McKnight, Diane M.; Bencala, K.E.

    1996-01-01

    Solute transport simulations quantitatively constrained hydrologic and geochemical hypotheses about field observations of a pH modification in an acid mine drainage stream. Carbonate chemistry, the formation of solid phases, and buffering interactions with the stream bed were important factors in explaining the behavior of pH, aluminum, and iron. The precipitation of microcrystalline gibbsite accounted for the behavior of aluminum; precipitation of Fe(OH)3 explained the general pattern of iron solubility. The dynamic experiment revealed limitations on assumptions that reactions were controlled only by equilibrium chemistry. Temporal variation in relative rates of photoreduction and oxidation influenced iron behavior. Kinetic limitations on ferrous iron oxidation and hydrous oxide precipitation and the effects of these limitations on field filtration were evident. Kinetic restraints also characterized interaction between the water column and the stream bed, including sorption and desorption of protons from iron oxides at the sediment-water interface and post-injection dissolution of the precipitated aluminum solid phase.

  17. Silicon nitride-aluminum oxide solid solution (SiAION) formation and densification by pressure sintering

    NASA Technical Reports Server (NTRS)

    Yeh, H. C.; Sanders, W. A.; Fiyalko, J. L.

    1975-01-01

    Stirred-ball-mill-blended Si3N4 and Al2O3 powders were pressure sintered in order to investigate the mechanism of solid solution formation and densification in the Si3N4-Al2O3 system. Powder blends with Si3N4:Al2O3 mole ratios of 4:1, 3:2, and 2:3 were pressure sintered at 27.6-MN/sq m pressure at temperatures to 17000 C (3090 F). The compaction behavior of the powder blends during pressure sintering was determined by observing the density of the powder compact as a function of temperature and time starting from room temperature. This information, combined with the results of X-ray diffraction and metallographic analyses regarding solutioning and phase transformation phenomena in the Si3N4-Al2O3 system, was used to describe the densification behavior.

  18. Fractionation of residual Al in natural water treatment from reservoir with poly-aluminum-silicate-chloride (PASiC): effect of OH/Al, Si/Al molar ratios and initial pH.

    PubMed

    Yang, Zhonglian; Gao, Baoyu; Wang, Yan; Zhao, Yaqin; Yue, Qinyan

    2012-01-01

    An aluminum fractionation study was conducted for a surface reservoir water treatment to understand the performance of poly-aluminum-silicate-chloride (PASiC) in terms of the residual Al fractions as a function of initial pH. The coagulation performance expressed as turbidity and organic matter removal was established as supporting data. Some extra data were evaluated in terms of the residual Al ratio of the composite PASiC coagulant. The main residual Al sources were the Al fractions derived from the use of PASiC. The turbidity and organic matter removal ability was optimal at initial pH 6.00-7.00, while the concentrations of various residual Al species and the residual Al ratio of PASiC were minimal at an initial pH range of 7.00-8.00. Under the conditions of OH/Al molar ratio = 2.00 and Si/Al molar ratio = 0.05, PASiC had superior coagulation performance and comparatively low residual Al concentrations. The Al fraction in the composite PASiC coagulant seldom remained under such conditions. Experimental data also indicated that the suspended (filterable) Al fraction was the dominant species, and organic-bound or organo-Al complex Al was considered to be the major species of dissolved Al in water treated by PASiC coagulation. Additionally, the dissolved inorganic monomeric Al species dominated the dissolved monomeric Al fraction.

  19. Concentration dependence of ionic conductance measured with ion-selective sub-micro pipette probes in aqueous sodium and potassium chloride solutions

    NASA Astrophysics Data System (ADS)

    Son, J. W.; Takami, T.; Lee, J.-K.; Kawai, T.; Park, B. H.

    2011-07-01

    Selective ionic currents in aqueous sodium and potassium chloride solutions with concentrations from 0.01 M to 1.0 M were measured using sub-micro pipette probes in which a poly(vinyl chloride) film containing crown ethers selectively filtered sodium or potassium ions. The selective ionic currents were monitored with a sub-picoampere current measurement system developed from the techniques of TΩ-gap impedance scanning tunneling microscopy. The ionic currents increased with the concentration of the corresponding solution, and thus these sub-micro pipette probes can be applied to detect local ionic concentration of a specific ion in living cells with ionic concentration higher than 0.1 M.

  20. Coagulation behavior and floc properties of compound bioflocculant-polyaluminum chloride dual-coagulants and polymeric aluminum in low temperature surface water treatment.

    PubMed

    Huang, Xin; Sun, Shenglei; Gao, Baoyu; Yue, Qinyan; Wang, Yan; Li, Qian

    2015-04-01

    This study was intended to compare coagulation behavior and floc properties of two dual-coagulants polyaluminum chloride-compound bioflocculant (PAC-CBF) (PAC dose first) and compound bioflocculant-polyaluminum chloride (CBF-PAC) (CBF dose first) with those of PAC alone in low temperature drinking water treatment. Results showed that dual-coagulants could improve DOC removal efficiency from 30% up to 34%. Moreover, CBF contributed to the increase of floc size and growth rate, especially those of PAC-CBF were almost twice bigger than those of PAC. However, dual-coagulants formed looser and weaker flocs with lower breakage factors in which fractal dimension of PAC-CBF flocs was low which indicates a looser floc structure. The floc recovery ability was in the following order: PAC-CBF>PAC alone>CBF-PAC. The flocculation mechanism of PAC was charge neutralization and enmeshment, meanwhile the negatively charged CBF added absorption and bridging effect.

  1. Stability, compatibility and plasticizer extraction of quinine injection added to infusion solutions and stored in polyvinyl chloride (PVC) containers.

    PubMed

    Faouzi, M A; Khalfi, F; Dine, T; Luyckx, M; Brunet, C; Gressier, B; Goudaliez, F; Cazin, M; Kablan, J; Belabed, A; Cazin, J C

    1999-12-01

    The stability of quinine was determined in various diluents and in polyvinyl chloride (PVC) containers. The release of diethyhexyl phthalate (DEHP) from PVC bags into intravenous infusions of quinine was also measured. We used an injection of two doses of quinine; quiniforme at 500 mg and quinimax at 400 mg in either 250- or 500-ml PVC infusion bags containing 5% dextrose, to give initial nominal concentrations of 2 or 1 mg ml(-1) quiniforme and 1.6 or 0.8 mg ml(-1) quinimax, the mean concentrations commonly used in clinical practice. Samples were assayed by stability-indicating high-performance liquid chromatography (HPLC) and the clarity was determined visually. Experiments were conducted to determine whether the stability and compatibility of quinine would be compromised, and whether DEHP would be leached from PVC bags and PVC administration sets during storage and simulated infusion. There was no substantial loss of quiniforme and quinimax over 1- or 2-h simulated infusion irrespective of the diluent, and storage during 8 h at 22 degrees C, 48 or 72 h at 4 degrees C and 96 h at 45 degrees C. Leaching of DEHP was also detected during simulated infusion delivery using PVC bags and PVC administration sets. The quantity was less than 2 microg ml(-1). During storage at 4 degrees C and room temperature the leaching of DEHP was low, but when the temperature was 45 degrees C the quantity was high, 21 microg ml(-1). To minimise patient exposure to DEHP, quinine solutions with all drugs should be infused immediately or stored for a maximum of 48 h at 4 degrees C.

  2. The development of BCB-sealed galvanic cells. Case study: aluminum-platinum cells activated with sodium hypochlorite electrolyte solution

    NASA Astrophysics Data System (ADS)

    Dlutowski, J.; Biver, C. J.; Wang, W.; Knighton, S.; Bumgarner, J.; Langebrake, L.; Moreno, W.; Cardenas-Valencia, A. M.

    2007-08-01

    Energy on demand is an important concept in remote sensor development. The fabrication process for silicon-wafer-based, totally enclosed galvanic cells is presented herein. Benzocyclyobutene (BCB), a photo-patternable material, is used as the adhesive layer between the silicon wafers on which metal electrodes are patterned to form the cells' electrolyte cavity. As a case study, and since aluminum is an anode material with thermodynamic high energy density, this metal is evaporated onto a wafer and used as an anode. A sputtered platinum film collects the charge and provides a catalytic surface in the cell cathode. The metal film patterning process and wafer-to-wafer bonding with BCB is detailed. The difficulties encountered, and design modifications to overcome these, are presented. Cells of the mentioned design were activated with sodium hypochlorite solution electrolyte. Typical potential outputs for the cells, as a function of operational time, are also presented. With a 5 kΩ load, a potential of 1.4 V was maintained for over 240 min, until depletion of the electrolyte occurred. Average cell energy outputs under electrical loads between 100 Ω and 5 kΩ were in the range of 4-10 J with columbic densities ranging from 45 to 83 Ah L-1.

  3. PROCESS FOR REMOVING ALUMINUM COATINGS

    DOEpatents

    Flox, J.

    1959-07-01

    A process is presented for removing aluminum jackets or cans from uranium slugs. This is accomplished by immersing the aluminum coated uranium slugs in an aqueous solution of 9 to 20% sodium hydroxide and 35 to 12% sodium nitrate to selectively dissolve the aluminum coating, the amount of solution being such as to obtain a molar ratio of sodium hydroxide to aluminum of at least

  4. Universal charge quenching and stability of proteins in 1-methyl-3-alkyl (hexyl/octyl) imidazolium chloride ionic liquid solutions.

    PubMed

    Rawat, Kamla; Bohidar, H B

    2012-09-13

    This study reports pH dependent stability of protein dispersions of five common proteins, bovine serum albumin (BSA), human serum albumin (HSA), immunoglobulin (IgG), β-lactoglobulin (β-Lg), and gelatin-B (Gel-B), all having isoelectric pH, pI ≈ 5, in room temperature ionic liquid solutions of 1-methyl-3-alkyl (hexyl/octyl) imidazolium chloride (concentration 0-0.2% w/v). Molecular hydrophobicity index, (H-index = hydrophobicity/hydrophilicity) of these molecules spanned the range 0.43-0.87. Electrophoretic characteristics, surface tension data and hydrodynamic size information revealed that IL solutions provide dispersion stability owing to specific protein-IL binding which did not alter their pI values though their surface charge was considerably screened. Change in maximum (ζ(max)) and minimum (ζ(min)) zeta potential values observed at pH ~3 (maximum protonated state) and pH ~8 (maximum deprotonated state) could be described universally as function of IL concentration, c as Δζ(x) = [1 - exp(-ac)] where Δζ(x) is either |(ζ(max) - ζ(w))|/ζ(w) or |(ζ(min) - ζ(w))|/ζ(w), and ζ(w) is the corresponding value in water. Tensiometry data showed two major stages of protein-IL interactions: (i) for c < cmc of IL, the IL molecules selectively bind with imidazolium cation through electrostatic forces forming protein-IL (complex) and (ii) for c> cmc free IL-aggregates begin to form. Similarly, we can define Δγ(x) as either |(γ(max) - γ(w))|/γ(w) at pH 3 or |(γ(min) - γ(w))|/γ(w) at pH 8. Both Δζ(x) and Δγ(x) showed linear dependence with c, Δγ(min, max) (or Δζ(min, max)) = (1 - K(γ) (or K(ζ)) H-index), where the slopes K(ζ) and K(γ) defined intermolecular interactions. Hydrodynamic radii data revealed protein stabilization, circular dichroism spectra implied retention of secondary structures, and Raman spectra confirmed a marginal increase in water structure. Results concluded that selective binding of IL molecules to protein surface in

  5. Facile and environmentally friendly solution-processed aluminum oxide dielectric for low-temperature, high-performance oxide thin-film transistors.

    PubMed

    Xu, Wangying; Wang, Han; Xie, Fangyan; Chen, Jian; Cao, Hongtao; Xu, Jian-Bin

    2015-03-18

    We developed a facile and environmentally friendly solution-processed method for aluminum oxide (AlOx) dielectrics. The formation and properties of AlOx thin films under various annealing temperatures were intensively investigated by thermogravimetric analysis-differential scanning calorimetry (TGA-DSC), X-ray diffraction (XRD), spectroscopic ellipsometry, atomic force microscopy (AFM), attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR), X-ray photoelectron spectroscopy (XPS), impedance spectroscopy, and leakage current measurements. The sol-gel-derived AlOx thin film undergoes the decomposition of organic residuals and nitrate groups, as well as conversion of aluminum hydroxides to form aluminum oxide, as the annealing temperature increases. Finally, the AlOx film is used as gate dielectric for a variety of low-temperature solution-processed oxide TFTs. Above all, the In2O3 and InZnO TFTs exhibited high average mobilities of 57.2 cm(2) V(-1) s(-1) and 10.1 cm(2) V(-1) s(-1), as well as an on/off current ratio of ∼10(5) and low operating voltages of 4 V at a maximum processing temperature of 300 °C. Therefore, the solution-processable AlOx could be a promising candidate dielectric for low-cost, low-temperature, and high-performance oxide electronics.

  6. Improvement of abrasion resistance in artificial seawater and corrosion resistance in NaCl solution of 7075 aluminum alloy processed by laser shock peening

    NASA Astrophysics Data System (ADS)

    Wang, Hao; Ning, Chengyi; Huang, Yihui; Cao, Zhenya; Chen, Xiaoxiao; Zhang, Wenwu

    2017-03-01

    As 7075 aluminum alloy is widely used in a humid environment, in order to enhance its abrasion resistance and electrochemical corrosion resistance, the paper studied the effect of laser shock peening on abrasion resistance in artificial seawater and corrosion resistance in 3.5% NaCl solution of 7075 aluminum alloy. Result shows that when specimens were treated once and twice with 7.17 GW/cm2 the abrasion loss would be reduced by 43.75% and 46.09% compare to untreated respectively, and the corrosion rate of 7075 aluminum alloy could be reduced as much as 50.32% by LSP treatment with 7.17 GW/cm2. What's more, the effects on the microhardness, microstructure and residual stress with different LSP impacts and power density were investigated to find out strengthening mechanism of laser shock peening, which were observed and measured by microhardness tester, optical microscope and X-ray diffraction (XRD) residual stress tester. In the entire laboratory tests, it is considered that LSP is a practical option to improve abrasion resistance in seawater and corrosion resistance of 7075 aluminum alloy.

  7. Effect of chloride ions on the corrosion behavior of low-alloy steel containing copper and antimony in sulfuric acid solution

    NASA Astrophysics Data System (ADS)

    Park, Sun-Ah; Kim, Seon-Hong; Yoo, Yun-Ha; Kim, Jung-Gu

    2015-05-01

    The influence of the addition of HCl on the corrosion behavior of low-alloy steel containing copper and antimony was investigated using electrochemical (potentiodynamic and potentiostatic polarization tests, and electrochemical impedance spectroscopy) and weight loss tests in a 1.6M H2SO4 solution with different concentrations of hydrochloric acid (0.00, 0.08, 0.15 and 0.20 M HCl) at 60 °C. The result showed that the corrosion rate decreased with increasing HCl by the formation of protective layers. SEM, EDS and XPS examinations of the corroded surfaces after the immersion test indicated that the corrosion production layer formed in the solution containing HCl was highly comprised of metallic Cu, Cu chloride and metallic (Fe, Cu, Sb) compounds. The corrosion resistance was improved by the Cu-enriched layer, in which chloride ions are an accelerator for cupric ion reduction during copper deposition. Furthermore, cuprous and antimonious chloride species are complex salts for cuprous ions adsorbed on the surface during copper deposition.

  8. An empirical equation with tables of smoothed solubilities of methane in water and aqueous sodium chloride solutions up to 25 weight percent, 360 degrees C, and 138 MPa

    USGS Publications Warehouse

    Haas, John L.

    1978-01-01

    The total pressure for the system H2O-CH 4 is given by p(total) = P(H2O,t) + exp10[log x(CH 4) - a - b x(CH4)], where P(H2O,t) is the vapor pressure of H2O liquid at the temperature t (?C) and x(CH 4) is the molal concentration of methane in the solution. The terms a and b are functions of temperature only. Where the total pressure and temperature are known, the concentration of methane, x(CH4), is found by iteration. The concentration of methane in a sodium chloride brine, y(CH4), is estimated using the function log y(CH4) = log x(CH4) - A I, where A is the salting out constant and I is the ionic strength. For sodium chloride solutions, the ionic strength is equal to the molality of the salt. The equations are valid to 360?C, 138 MPa, and 25 weight percent sodium chloride.

  9. Collective hydration dynamics of guanidinium chloride solutions and its possible role in protein denaturation: a terahertz spectroscopic study.

    PubMed

    Samanta, Nirnay; Mahanta, Debasish Das; Mitra, Rajib Kumar

    2014-11-14

    The remarkable ability of guanidinium chloride (GdmCl) to denature proteins is a well studied yet controversial phenomenon; the exact molecular mechanism is still debatable, especially the role of hydration dynamics, which has been paid less attention. In the present contribution, we have addressed the issue of whether the collective hydrogen bond dynamics of water gets perturbed in the presence of GdmCl and its possible impact on the denaturation of a globular protein human serum albumin (HSA), using terahertz (THz) time domain spectroscopy (TTDS) in the frequency range of 0.3-2.0 THz. The collective hydrogen bond dynamics is determined by fitting the obtained complex dielectric response in a multiple Debye relaxation model. To compare the results, the studies were extended to two more salts: tetramethylguanidinium chloride (TMGdmCl) and sodium chloride (NaCl). It was concluded that the change in hydration dynamics plays a definite role in the protein denaturation process.

  10. Volume regulation in mammalian skeletal muscle: the role of sodium–potassium–chloride cotransporters during exposure to hypertonic solutions

    PubMed Central

    Lindinger, Michael I; Leung, Matthew; Trajcevski, Karin E; Hawke, Thomas J

    2011-01-01

    Abstract Controversy exists as to whether mammalian skeletal muscle is capable of volume regulation in response to changes in extracellular osmolarity despite evidence that muscle fibres have the required ion transport mechanisms to transport solute and water in situ. We addressed this issue by studying the ability of skeletal muscle to regulate volume during periods of induced hyperosmotic stress using single, mouse extensor digitorum longus (EDL) muscle fibres and intact muscle (soleus and EDL). Fibres and intact muscles were loaded with the fluorophore, calcein, and the change in muscle fluorescence and width (single fibres only) used as a metric of volume change. We hypothesized that skeletal muscle exposed to increased extracellular osmolarity would elicit initial cellular shrinkage followed by a regulatory volume increase (RVI) with the RVI dependent on the sodium–potassium–chloride cotransporter (NKCC). We found that single fibres exposed to a 35% increase in extracellular osmolarity demonstrated a rapid, initial 27–32% decrease in cell volume followed by a RVI which took 10–20 min and returned cell volume to 90–110% of pre-stimulus values. Within intact muscle, exposure to increased extracellular osmolarity of varying degrees also induced a rapid, initial shrinkage followed by a gradual RVI, with a greater rate of initial cell shrinkage and a longer time for RVI to occur with increasing extracellular tonicities. Furthermore, RVI was significantly faster in slow-twitch soleus than fast-twitch EDL. Pre-treatment of muscle with bumetanide (NKCC inhibitor) or ouabain (Na+,K+-ATPase inhibitor), increased the initial volume loss and impaired the RVI response to increased extracellular osmolarity indicating that the NKCC is a primary contributor to volume regulation in skeletal muscle. It is concluded that mouse skeletal muscle initially loses volume then exhibits a RVI when exposed to increases in extracellular osmolarity. The rate of RVI is dependent

  11. Volume regulation in mammalian skeletal muscle: the role of sodium-potassium-chloride cotransporters during exposure to hypertonic solutions.

    PubMed

    Lindinger, Michael I; Leung, Matthew; Trajcevski, Karin E; Hawke, Thomas J

    2011-06-01

    Controversy exists as to whether mammalian skeletal muscle is capable of volume regulation in response to changes in extracellular osmolarity despite evidence that muscle fibres have the required ion transport mechanisms to transport solute and water in situ. We addressed this issue by studying the ability of skeletal muscle to regulate volume during periods of induced hyperosmotic stress using single, mouse extensor digitorum longus (EDL) muscle fibres and intact muscle (soleus and EDL). Fibres and intact muscles were loaded with the fluorophore, calcein, and the change in muscle fluorescence and width (single fibres only) used as a metric of volume change. We hypothesized that skeletal muscle exposed to increased extracellular osmolarity would elicit initial cellular shrinkage followed by a regulatory volume increase (RVI) with the RVI dependent on the sodium–potassium–chloride cotransporter (NKCC). We found that single fibres exposed to a 35% increase in extracellular osmolarity demonstrated a rapid, initial 27–32% decrease in cell volume followed by a RVI which took 10-20 min and returned cell volume to 90–110% of pre-stimulus values. Within intact muscle, exposure to increased extracellular osmolarity of varying degrees also induced a rapid, initial shrinkage followed by a gradual RVI, with a greater rate of initial cell shrinkage and a longer time for RVI to occur with increasing extracellular tonicities. Furthermore, RVI was significantly faster in slow-twitch soleus than fast-twitch EDL. Pre-treatment of muscle with bumetanide (NKCC inhibitor) or ouabain (Na+,K+-ATPase inhibitor), increased the initial volume loss and impaired the RVI response to increased extracellular osmolarity indicating that the NKCC is a primary contributor to volume regulation in skeletal muscle. It is concluded that mouse skeletal muscle initially loses volume then exhibits a RVI when exposed to increases in extracellular osmolarity. The rate of RVI is dependent on the

  12. Calcium Chloride in Neonatal Parenteral Nutrition Solutions with and without Added Cysteine: Compatibility Studies Using Laser and Micro-Flow Imaging Methodology

    PubMed Central

    Huston, Robert K.; Christensen, J. Mark; Alshahrani, Sultan M.; Mohamed, Sumeia M.; Clark, Sara M.; Nason, Jeffrey A.; Wu, Ying Xing

    2015-01-01

    Background Previous studies of compatibility of calcium chloride (CaCl2) and phosphates have not included particle counts in the range specified by the United States Pharmacopeia. Micro-flow imaging techniques have been shown to be comparable to light obscuration when determining particle count and size in pharmaceutical solutions. Objective The purpose of this study was to do compatibility testing for parenteral nutrition (PN) solutions containing CaCl2 using dynamic light scattering and micro-flow imaging techniques. Methods Solutions containing TrophAmine (Braun Medical Inc, Irvine, CA), CaCl2, and sodium phosphate (NaPhos) were compounded with and without cysteine. All solutions contained standard additives to neonatal PN solutions including dextrose, trace metals, and electrolytes. Control solutions contained no calcium or phosphate. Solutions were analyzed for particle size and particle count. Means of Z-average particle size and particle counts of controls were determined. Study solutions were compared to controls and United States Pharmacopeia (USP) Chapter 788 guidelines. The maximum amount of Phos that was compatible in solutions that contained at least 10 mmol/L of Ca in 2.5% amino acids (AA) was determined. Compatibility of these solutions was verified by performing analyses of 5 repeats of these solutions. Microscopic analyses of the repeats were also performed. Results Amounts of CaCl2 and NaPhos that were compatible in solutions containing 1.5%, 2%, 2.5%, and 3% AA were determined. The maximum amount of NaPhos that could be added to TrophAmine solutions of > = 2.5% AA containing at least 10 mmol/L of CaCl2 was 7.5 mmol/L. Adding 50 mg/dL of cysteine increased the amount of NaPhos that could be added to solutions containing 10 mmol/L of CaCl2 to 10 mmol/L. Conclusion Calcium chloride can be added to neonatal PN solutions containing NaPhos in concentrations that can potentially provide an intravenous intake of adequate amounts of calcium and phosphorus

  13. XPS depth profiling study on the passive oxide film of carbon steel in saturated calcium hydroxide solution and the effect of chloride on the film properties

    NASA Astrophysics Data System (ADS)

    Ghods, P.; Isgor, O. B.; Brown, J. R.; Bensebaa, F.; Kingston, D.

    2011-03-01

    X-ray photoelectron spectroscopy (XPS) was used to study the properties of passive oxide film that form on carbon steel in saturated calcium hydroxide solution and the effect of chloride on the film properties. The thickness of the oxide films was determined to be approximately 4 nm and was not affected by the exposure time. Near the film/substrate interface the concentration of the Fe2+ oxides was higher than the concentration of the Fe3+ oxides; the layers near the free surface of the film mostly contained Fe3+ oxides. Chloride exposure decreased the thickness of the oxide films and changed their stoichiometry such that near the film/substrate interface Fe3+/Fe2+ ratio increased.

  14. Lithium Sulfuryl Chloride Battery.

    DTIC Science & Technology

    Primary batteries , Electrochemistry, Ionic current, Electrolytes, Cathodes(Electrolytic cell), Anodes(Electrolytic cell), Thionyl chloride ...Phosphorus compounds, Electrical conductivity, Calibration, Solutions(Mixtures), Electrical resistance, Performance tests, Solvents, Lithium compounds

  15. Chloride removal from vitrification offgas

    SciTech Connect

    Slaathaug, E.J.

    1995-06-01

    This study identified and investigated techniques of selectively purging chlorides from the low-level waste (LLW) vitrification process with the purge stream acceptable for burial on the Hanford Site. Chlorides will be present in high concentration in several individual feeds to the LLW Vitrification Plant. The chlorides are highly volatile in combustion type melters and are readily absorbed by wet scrubbing of the melter offgas. The Tank Waste Remediation System (TWRS) process flow sheets show that the resulting chloride rich scrub solution is recycled back to the melter. The chlorides must be purged from the recycle loop to prevent the buildup of excessively high chloride concentrations.

  16. A Solution NMR Investigation into the Early Events of Amelogenin Nanosphere Self-Assembly Initiated with Sodium Chloride or Calcium Chloride

    SciTech Connect

    Buchko, Garry W.; Tarasevich, Barbara J.; Bekhazi, Jacky G.; Snead, Malcolm L.; Shaw, Wendy J.

    2008-12-08

    Using solution-state NMR spectroscopy, new insights into the early intermolecular interactions stabilizing amelogenin supramolecular assembly and the potential role of calcium ions have been discovered. Two-dimensional 1H-15N spectra were recorded for 15N-labeled amelogenin as a function of increasing Ca2+ concentration starting from monomeric conditions. Evidence for protein-protein interactions were observed between residues E18 and E40 in the N-terminus. At higher Ca2+ concentrations there was concurrent involvement of residues in both the N- (Y12-Q56) and the C-terminus (Q144-T171). Neither specific residues nor their stepwise interaction have previously been identified in the initial stages of nanosphere assembly.

  17. Effect of OH-/Al3+ and Si/Al molar ratios on the coagulation performance and residual Al speciation during surface water treatment with poly-aluminum-silicate-chloride (PASiC).

    PubMed

    Yang, Zhonglian; Gao, Baoyu; Xu, Weiying; Cao, Baichuan; Yue, Qinyan

    2011-05-15

    Coagulation performance, mechanism of poly-aluminum-silicate-chloride (PASiC) and residual Al speciation in the effluent with respect to a specific surface water treatment in China were comprehensively investigated in this study. The impact of OH(-)/Al(3+) and Si/Al molar ratios on the coagulation performance, mechanism and residual Al speciation of PASiC in surface water treatment was discussed as a function of coagulant dosage. It was intended to provide an insight into the relationship between coagulation performance and residual Al. Experimental results revealed that when OH(-)/Al(3+) molar ratio = 2.00 and Si/Al molar ratio = 0.0500 in PASiC coagulant, PASiC exhibited beneficial coagulation property and relatively lower content of residual Al. Surface bridging and entrapment was more effective compared with charge neutralization during the specific surface water treatment. The majority of residual Al in the effluent existed in the form of insoluble suspended or particulate Al. Dissolved organically bound Al was almost the major speciation in dissolved Al and dissolved inorganically bound monomeric Al was the only component in dissolved monomeric Al. Al in PASiC remained abundant at lower dosages and residual Al concentration could be effectively reduced at the dosages of 12.0-15.0mg/L as Al.

  18. Generation of sodium hypochlorite (NaOCl) from sodium chloride solution using C/PbO2 and Pb/PbO2 electrodes

    NASA Astrophysics Data System (ADS)

    Ghalwa, Nasser Abu; Tamos, Hassan; ElAskalni, Mohamed; El Agha, Abed Rhman

    2012-06-01

    Two modified electrodes (Pb/PbO2 and C/PbO2) were prepared by electrodepositing a lead oxide layer on lead and carbon substrates. These modified electrodes were used as anodes for the generation of sodium hypochlorite (NaOCl) from sodium chloride solution. Different operating conditions and factors affecting the treatment process of NaOCl generation, including current density, pH values, conductive electrolytes, and electrolysis time, were studied and optimized. By comparison the C/PbO2 electrode shows a higher efficiency than the Pb/PbO2 electrode for the generation of NaOCl.

  19. Comparison of the kinetic laws of the dissolution of bauxite and aluminum and iron(III) oxides and hydroxides in hydrochloric acid

    NASA Astrophysics Data System (ADS)

    Gololobova, E. G.; Gorichev, I. G.; Lainer, Yu. A.; Kozlov, K. V.

    2013-07-01

    The influence of the temperature and concentration of a hydrochloric acid solution on the dissolution kinetics of aluminum and iron(III) oxides and hydroxides and a natural sample of aluminum-containing raw materials, bauxite, is studied. The rate W of the transition of iron(III) ions from bauxite is higher than the rate of aluminum ion transition. The dependence of the fraction of a dissolved solid phase on time τ of dissolution of the oxides and hydroxides is determined, α = 1 — exp(- Asinh( Wτ)). The solubility of iron(III) chloride increases and that of aluminum chloride decreases as the HCl concentration increases. An empirical equation is proposed for the description of the dependence of the process rate on a series of parameters,.

  20. VOLATILE CHLORIDE PROCESS FOR THE RECOVERY OF METAL VALUES

    DOEpatents

    Hanley, W.R.

    1959-01-01

    A process is presented for recovering uranium, iron, and aluminum from centain shale type ores which contain uranium in minute quantities. The ore is heated wiih a chlorinating agent. such as chlorine, to form a volatilized stream of metal chlorides. The chloride stream is then passed through granular alumina which preferentially absorbs the volatile uranium chloride and from which the uranium may later be recovered. The remaining volatilized chlorides, chiefly those of iron and aluminum, are further treated to recover chlorine gas for recycle, and to recover ferric oxide and aluminum oxide as valuable by-products.

  1. Vapor Pressure of Aluminum Chloride Systems. 3. Vapor Pressure of Aluminum Chloride-Sodium Chloride Melts

    DTIC Science & Technology

    1977-06-23

    were all as described previously (10). A .XCp/R log T(1, 2). mercury manometer was used as n additional external piessure The data were least-squares...the use of a mercury manometer and a NMLeod gauge, respectively, for pressure measurement; all other pressure measurements were made with a

  2. PREPARATION OF URANIUM-ALUMINUM ALLOYS

    DOEpatents

    Moore, R.H.

    1962-09-01

    A process is given for preparing uranium--aluminum alloys from a solution of uranium halide in an about equimolar molten alkali metal halide-- aluminum halide mixture and excess aluminum. The uranium halide is reduced and the uranium is alloyed with the excess aluminum. The alloy and salt are separated from each other. (AEC)

  3. Removal of tetrafluoroborate ion from aqueous solution using magnesium-aluminum oxide produced by the thermal decomposition of a hydrotalcite-like compound.

    PubMed

    Yoshioka, Toshiaki; Kameda, Tomohito; Miyahara, Motoya; Uchida, Miho; Mizoguchi, Tadaaki; Okuwaki, Akitsugu

    2007-10-01

    Magnesium-aluminum oxide (Mg-Al oxide) prepared by the thermal decomposition of a hydrotalcite-like compound was found to have potential for treating NaBF(4) wastewater. The Mg-Al oxide removed the BF(4)(-) and F(-) and H(3)BO(3) from the NaBF(4) solution. With increasing Mg-Al oxide quantity and time, the BF(4)(-) concentration decreased and the degree of BF(4)(-), F(-), and boron removal increased. The decrease in the BF(4)(-) concentration resulted from uptake by the Mg-Al oxide and not hydrolysis. The Mg-Al oxide took up F(-) from the solution preferentially. The Mg-Al oxide also converted the H(3)BO(3) in the aqueous solution into H(2)BO(3)(-), which it took up.

  4. Phonon spectroscopy of the low-energy excitations in the solid solutions of yttrium–rare-earth metal–aluminum garnets

    SciTech Connect

    Khazanov, E. N. Taranov, A. V.; Shevchenko, E. V.; Charnaya, E. V.

    2015-07-15

    The transport characteristics of thermal-frequency phonons and the specific heat of a series of single crystals of yttrium–rare-earth metal–aluminum garnet solid solutions are studied at the helium temperatures. It is found that the existence of low-energy levels of various origins, which are responsible for an increase in the specific heat, retards phonon transport by one–three orders of magnitude. The temperature dependences of specific heat and the kinetic characteristics of phonons have a similar character.

  5. 21 CFR 184.1138 - Ammonium chloride.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... GRAS § 184.1138 Ammonium chloride. (a) Ammonium chloride (NH4Cl, CAS Reg. No. 12125-02-9) is produced by the reaction of sodium chloride and an ammonium salt in solution. The less soluble sodium salt... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Ammonium chloride. 184.1138 Section 184.1138...

  6. Evaluated activity and osmotic coefficients for aqueous solutions: Bi-univalent compounds of zinc, cadmium, and ethylene bis(trimethylammonium) chloride and iodide

    NASA Astrophysics Data System (ADS)

    Goldberg, R. N.

    1981-01-01

    A critical evaluation of the mean activity and osmotic coefficients in aqueous solutions of eleven bi-univalent compounds of zinc and cadmium and ethylene bis(trimethylammonium) chloride and iodide at 298.15 K is presented. Osmotic coefficients were calculated from direct vapor pressure measurements, from isopiestic measurements and from freezing point depression measurements. Activity coefficients were calculated from electromotive force measurements on galvanic cells with and without transference. Given are empirical coefficients for three different correlating equations, obtained by a weighted least squares fit of the experimental data, and tables consisting of the activity coefficients of the compounds, the osmotic coefficients and activity of water, and the excess Gibbs energy of the solution as functions of the molality for each electrolyte system. The literature coverage is through the computerized version of Chemical Abstracts of September 1979.

  7. Preparation of Hard Oxide Films on Evaporated Aluminum Surfaces and Applications of Such Films

    DTIC Science & Technology

    1949-07-28

    Anodic coatings produced with various voltages (10 to 150 voltsT were released from their substrate by dissolving the aluminum in a solution of mercuric ...from its substrate in mercuric chloride, washed with dilute hydrochloric acid and distilled water, and mounted on a support screen for the electron...thallium halides and other snythetic And study of methods of shaping, grinding, and polishing ,fi such crystals, A ;l .ication of low reflectance coatings

  8. Time exposure studies on stress corrosion cracking of aluminum 2014-T6, 2219-T87, 2014-T651, 7075-T651, and titanium 6Al-4V

    NASA Technical Reports Server (NTRS)

    Terrell, J.

    1973-01-01

    The effect of a constant applied stress in crack initiation of aluminum 2014-T6, 2219-T87, 2014-T651, 7075-T651 and titanium 6Al-4V has been investigated. Aluminum c-ring specimens (1-inch diameter) and u-band titanium samples were exposed continuously to a 3.5% NaCl solution (pH 7) and organic fluids of ethyl, methyl, and iso-propyl alcohol (reagent purity), and demineralized distilled water. Corrosive action was observed to begin during the first and second day of constant exposure as evidenced by accumulation of hydrogen bubbles on the surface of stressed aluminum samples. However, titanium stressed specimens showed no reactions to its environment. Results of this investigation seems to suggest that aluminum 2014-T6, aluminum 7075-T651 and aluminum 2014-T651 are susceptible to stress corrosion cracking in chloride solution (NaCl), while aluminum 2219-T87 seem to resist stress corrosion cracking in sodium chloride at three levels of stress (25%, 50%, and 75% Y.S.). In organic fluids of methyl, ethyl, and iso-propyl alcohol, 2014-T6 and 7075-T651 did not fail by SCC; but 2014-T651 was susceptible to SCC in methly alcohol, but resistant in ethyl alcohol, iso-propyl alcohol and demineralized distilled water.

  9. Long-term cement corrosion in chloride-rich solutions relevant to radioactive waste disposal in rock salt - Leaching experiments and thermodynamic simulations

    NASA Astrophysics Data System (ADS)

    Bube, C.; Metz, V.; Bohnert, E.; Garbev, K.; Schild, D.; Kienzler, B.

    Low- and intermediate-level radioactive wastes are frequently solidified in a cement matrix. In a potential repository for nuclear wastes, the cementitious matrix is altered upon contact with solution and the resulting secondary phases may provide for significant retention of the radionuclides incorporated in the wastes. In order to assess the secondary phases formed upon corrosion in chloride-rich solutions, which are relevant for nuclear waste disposal in rock salt, leaching experiments were performed. Conventional laboratory batch experiments using powdered hardened cement paste in MgCl2-rich solutions were left to equilibrate for up to three years and full-scale cemented waste products were exposed to NaCl-rich and MgCl2-rich solutions for more than twenty years, respectively. Solid phase analyses revealed that corrosion of hardened cement in MgCl2-rich solutions advanced faster than in NaCl-rich solutions due to the extensive exchange of Mg from solution against Ca from the cementitious solid. Thermodynamic equilibrium simulations compared well to results at the final stages of the respective experiments indicating that close to equilibrium conditions were reached. At high cement product to brine ratios (>0.65 g mL-1), the solution composition in the laboratory-scale experiments was close to that of the full-scale experiments (cement to brine ratio of 2.5 g mL-1) in the MgCl2 systems. The present study demonstrates the applicability of thermodynamic methods used in this approach to adequately describe full-scale long-term experiments with cemented waste simulates.

  10. PREPARATION OF ACTINIDE-ALUMINUM ALLOYS

    DOEpatents

    Moore, R.H.

    1962-09-01

    BS>A process is given for preparing alloys of aluminum with plutonium, uranium, and/or thorium by chlorinating actinide oxide dissolved in molten alkali metal chloride with hydrochloric acid, chlorine, and/or phosgene, adding aluminum metal, and passing air and/or water vapor through the mass. Actinide metal is formed and alloyed with the aluminum. After cooling to solidification, the alloy is separated from the salt. (AEC)

  11. Removal of coagulant aluminum from water treatment residuals by acid.

    PubMed

    Okuda, Tetsuji; Nishijima, Wataru; Sugimoto, Mayo; Saka, Naoyuki; Nakai, Satoshi; Tanabe, Kazuyasu; Ito, Junki; Takenaka, Kenji; Okada, Mitsumasa

    2014-09-01

    Sediment sludge during coagulation and sedimentation in drinking water treatment is called "water treatment residuals (WTR)". Polyaluminum chloride (PAC) is mainly used as a coagulant in Japan. The recycling of WTR has been desired; one method for its reuse is as plowed soil. However, WTR reuse in this way is inhibited by the aluminum from the added PAC, because of its high adsorption capacity for phosphate and other fertilizer components. The removal of such aluminum from WTR would therefore be advantageous for its reuse as plowed soil; this research clarified the effect of acid washing on aluminum removal from WTR and on plant growth in the treated soil. The percentage of aluminum removal from raw WTR by sulphuric acid solution was around 90% at pH 3, the percentage decreasing to 40% in the case of a sun-dried sample. The maximum phosphate adsorption capacity was decreased and the available phosphorus was increased by acid washing, with 90% of aluminum removal. The enhancement of Japanese mustard spinach growth and the increased in plant uptake of phosphates following acid washing were observed.

  12. Removal of lead from aqueous solution by activated carbon prepared from Enteromorpha prolifera by zinc chloride activation.

    PubMed

    Li, Yanhui; Du, Qiuju; Wang, Xiaodong; Zhang, Pan; Wang, Dechang; Wang, Zonghua; Xia, Yanzhi

    2010-11-15

    Activated carbon was prepared from Enteromorpha prolifera (EP) by zinc chloride activation. The physico-chemical properties of EP-activated carbon (EPAC) were characterized by thermal stability, zeta potential and Boehm titration methods. The examination showed that EPAC has a porous structure with a high surface area of 1688 m(2)/g. Batch adsorption experiments were carried out to study the effect of various parameters such as initial pH, adsorbent dosage, contact time and temperature on Pb(II) ions adsorption properties by EPAC. The kinetic studies showed that the adsorption data followed a pseudo second-order kinetic model. The isotherm analysis indicated that the adsorption data can be represented by Freundlich isotherm model. Thermodynamic studies indicated that the adsorption reaction was a spontaneous and endothermic process.

  13. A conductance study of guanidinium chloride, thiocyanate, sulfate, and carbonate in dilute aqueous solutions: ion-association and carbonate hydrolysis effects.

    PubMed

    Hunger, Johannes; Neueder, Roland; Buchner, Richard; Apelblat, Alexander

    2013-01-17

    We study the conductance of dilute aqueous solutions for a series of guandinium salts at 298.15 K. The experimental molar conductivities were analyzed within the framework of the Quint-Viallard theory in combination with Debye-Hückel activity coefficients. From this analysis, we find no evidence for significant ion association in aqueous solutions of guanidinium chloride (GdmCl) and guanidinium thiocyanate (GdmSCN), and the molar conductivity of these electrolytes can be modeled assuming a complete dissociation. The limiting ionic conductivity of the guanidinium ion (Gdm(+)) is accurately determined to λ(Gdm(+)) = 51.45 ± 0.10 S cm(2) mol(-1). For the bivalent salts guanidinium sulfate (Gdm(2)SO(4)) and guanidinium carbonate (Gdm(2)CO(3)), the molar conductivities show small deviations from ideal (fully dissociated electrolyte) behavior, which are related to weak ion association in solution. Furthermore, for solutions of Gdm(2)CO(3), the hydrolysis of the carbonate anion leads to distinctively increased molar conductivities at high dilutions. The observed ion association is rather weak for all studied electrolytes and cannot explain the different protein denaturing activities of the studied guanidinium salts, as has been proposed previously.

  14. Differences in the way potassium chloride and sucrose solutions effect osmotic potential of significance to stomata aperture modulation.

    PubMed

    Cochrane, Thomas T; Cochrane, Thomas A

    2009-03-01

    Guard cell solution osmotic potential changes resulting in the opening and closing of stomata apertures follow an initial influx of potassium ions, their substitution with sucrose molecules and the subsequent reduction of the latter. To provide an insight into the osmotic mechanism of the changes, the new equation for calculating osmotic pressure, which equates the difference between the energy of pure water across a semi-permeable membrane interface with that of solution water, was used to compare the osmotic properties of KCl and sucrose. For sucrose solutions, the effect of the sucrose molecules in increasing the spacing of the solution water was mainly responsible for osmotic potential; this contrasted with K+ + Cl(-) ions where their spacing effect was only a little higher to that of water held to those ions. At solute concentrations giving an osmotic potential level of -3.0 MPa near that of turgid guard cells, the spacing effect on the potential of the unattached solution water molecules caused by sucrose, but in its theoretical absence, was estimated as -2.203 MPa compared with -1.431 MPa for KCl. In contrast, the potential attributed to water molecules firmly held to the K+ + Cl(-) ions was -1.212 MPa versus zero for sucrose. The potential to keep the sucrose molecules in solution was -0.797 MPa compared with -0.357 MPa for KCl. The findings illustrate that the way KCl effects osmotic pressure is very different to that of sucrose. It is concluded that stomata aperture modulation is closely linked to the osmotic properties of its guard cell solution solutes.

  15. CORROSION PROTECTION OF ALUMINUM

    DOEpatents

    Dalrymple, R.S.; Nelson, W.B.

    1963-07-01

    Treatment of aluminum-base metal surfaces in an autoclave with an aqueous chromic acid solution of 0.5 to 3% by weight and of pH below 2 for 20 to 50 hrs at 160 to 180 deg C produces an extremely corrosion-resistant aluminum oxidechromium film on the surface. A chromic acid concentration of 1 to 2% and a pH of about 1 are preferred. (D.C.W.)

  16. Corrosion Protection of Aluminum

    DOEpatents

    Dalrymple, R. S.; Nelson, W. B.

    1963-07-01

    Treatment of aluminum-base metal surfaces in an autoclave with an aqueous chromic acid solution of 0.5 to 3% by weight and of pH below 2 for 20 to 50 hrs at 160 to 180 deg C produces an extremely corrosion-resistant aluminum oxidechromium film on the surface. A chromic acid concentration of 1 to 2% and a pH of about 1 are preferred.

  17. Comparing polyaluminum chloride and ferric chloride for antimony removal.

    PubMed

    Kang, Meea; Kamei, Tasuku; Magara, Yasumoto

    2003-10-01

    Antimony has been one of the contaminants required to be regulated, however, only limited information has been collected to date regarding antimony removal by polyaluminium chloride (PACl) and ferric chloride (FC). Accordingly, the possible use of coagulation by PACl or FC for antimony removal was investigated. Jar tests were used to determine the effects of solution pH, coagulant dosage, and pre-chlorination on the removal of various antimony species. Although high-efficiency antimony removal by aluminum coagulation has been expected because antimony is similar to arsenic in that both antimony and arsenic are a kind of metalloid in group V of the periodic chart, this study indicated: (1) removal density (arsenic or antimony removed per mg coagulant) for antimony by PACl was about one forty-fifth as low as observed for As(V); (2) although the removal of both Sb(III) and Sb(V) by coagulation with FC was much higher than that of PACl, a high coagulant dose of 10.5mg of FeL(-1) at optimal pH of 5.0 was still not sufficient to meet the standard antimony level of 2 microg as SbL(-1) for drinking water when around 6 microg as SbL(-1) were initially present. Consequently, investigation of a more appropriate treatment process is necessary to develop economical Sb reduction; (3) although previous studies concluded that As(V) is more effectively removed than As(III), this study showed that the removal of Sb(III) by coagulation with FC was much more pronounced than that of Sb(V); (4) oxidation of Sb(III) with chlorine decreased the ability of FC to remove antimony. Accordingly, natural water containing Sb(III) under anoxic condition should be coagulated without pre-oxidation.

  18. Aluminum Hydroxide

    MedlinePlus

    Aluminum hydroxide is used for the relief of heartburn, sour stomach, and peptic ulcer pain and to ... Aluminum hydroxide comes as a capsule, a tablet, and an oral liquid and suspension. The dose and ...

  19. Comparison of the release behaviors of di (2-ethylhexyl) phthalate and tri(2-ethylhexyl) trimellitate from the polyvinyl-chloride infusion set into pharmaceutical solutions.

    PubMed

    Zhang, Hong; Yang, Fengmin; Shen, Gang; Yang, Yueyang; Tang, Yalin

    2015-05-01

    Polyvinyl-chloride (PVC) with plasticizers of di(2-ethylhexyl) phthalate (DEHP) and tris(2-ethyl- hexyl) trimellitate (TOTM) is widely used in medical and paramedical appliances. However, such plasticizers can leach from PVC products into contact solutions. The aim of this study is to investigate the release behaviors of DEHP and TOTM from the PVC intravenous infusion set into various pharmaceutical solutions under the simulated clinical conditions, such as the lipophilic substances (paclitaxel) , parenteral nutrition (fat emulsion injection) , acid and alkali pharmaceutical solution (levofloxacin hydrochloride injection, pH 3.0-5.0 and furosemide, pH 8.0-9.0). A simple and rapid high-performance liquid chromatographic method with UV detection (HPLC-UV) for the determination of DEHP or TOTM released from PVC medical devices into the above intravenous preparations was developed. The cumulative amounts of DEHP or TOTM released in 24 h were in the same following order: paclitaxel > fat emulsion injection levofloxacin hydrochloride > furosemide solution. From a comparison of the cumulative amounts of released DEHP and TOTM from the above solutions, we found that the cumulative amount of TOTM is far less than that of DEHP, under the same conditions. The cumulative amount of the DEHP released in 24 h in the paclitaxel solution was 21. 14 mg, while under the same conditions, the cumulative amount of TOTM was only 0. 078 mg. The cumulative amount of DEHP is assumed to be about 270 times that of the released TOTM. Thus TOTM could be a superior alternative to DEHP for use in medical devices because of its potential lower leachability.

  20. Cytotoxicity of five fluoroquinolone and two nonsteroidal anti-inflammatory benzalkonium chloride-free ophthalmic solutions in four corneoconjunctival cell lines

    PubMed Central

    Ayaki, Masahiko; Iwasawa, Atsuo; Soda, Mitsutaka; Yaguchi, Shigeo; Koide, Ryohei

    2010-01-01

    Purpose: Epithelial disorders after eye surgery can result in visual deterioration and patient discomfort. Such disorders may be caused by drug toxicity. In the present study, we evaluated the toxicity of ophthalmic solutions, with or without benzalkonium chloride (BAK) as the preservative, used for postoperative care. Methods: A range of commercially available antibiotic and anti-inflammatory ophthalmic solutions used postoperatively (ie, levofloxacin, moxifloxacin, gatifloxacin, norfloxacin, tosufloxacin, dibekacin, cefmenoxime, diclofenac, bromfenac, pranoprofen, betamethasone, and fluoromethorone) were assessed in three corneal cell lines and one conjunctival cell line. All antibiotic solutions were BAK free. Cell viability was determined with the 3-(4,5-dimethyl-2 thiazoyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay after cells had been exposed to the drugs for 48 h. The effects of preservatives on cell viability were also determined. Toxicity was compared using the cell viability score (CVS). Results: Based on results of the MTT assay and CVS, the order of cell viability after exposure to the antibiotic solutions was cefmenoxime ≥ tosufloxicin ≥ dibekacin ≥ levofloxacin ≥ norfloxacin = gatifloxacin = moxifloxacin. For the anti-inflammatory solutions, the order of cell viability was betamethasone ≥ betamethasone + fradiomycin > preservative-free diclofenac ≥ preservative-free bromfenac >> 0.02% fluoromethorone ≥ 0.1% fluoromethorone = diclofenac + preservative = bromfenac + preservative = pranoprofen. The anti-inflammatory drugs were more toxic than the antibiotics. The toxicity of antibiotic drugs against ocular surface cells was dependent on the pharmaceutical components of the solution, whereas that of the anti-inflammatory drugs was dependent on both the pharmaceutical components and the preservatives. Conclusion: Postoperative drug-induced epitheliopathy may be caused primarily by anti-inflammatory drugs. CVS is useful in comparing the

  1. Laboratory studies of the low-temperature deliquescence of calcium chloride salts: Relevance to aqueous solutions on Mars and in the Antarctic Dry Valleys

    NASA Astrophysics Data System (ADS)

    Gough, R. V.; Chevrier, V.; Tolbert, M. A.

    2013-12-01

    There is significant interest in the possible existence of liquid water on current Mars. This water would likely exist as a brine in order to be stable on Mars today. It has been proposed that soil salts could form aqueous solutions through either the melting of ice by low-eutectic salts, or by the deliquescence of hygroscopic salts present in the Martian soil. The focus thus far has largely been on perchlorate species, which can melt ice at temperatures as low as 206 K and can deliquesce at relative humidity values as low as 38% RH. A Mars-relevant salt that has been neglected thus far is calcium chloride (CaCl2). Calcium has been reported to be an abundant cation at the Phoenix landing site and Mars Science Laboratory instruments have recently identified calcium as well. Simulations suggest subsurface CaCl2 is an ideal candidate to produce brines with seasonality consistent with observed recurring slope lineae (RSL) (Chevrier et al., 2012). Finally, the only terrestrial site where RSL-like features have been observed (near Don Juan Pond in the Antarctic Dry Valleys) contains abundant CaCl2. These seasonal slope streaks are thought to form when CaCl2 in the soil deliquesces due to contact with atmospheric water vapor (Dickson et al., 2013). It is important to understand how this CaCl2 interacts with water vapor at low temperatures relevant to Mars and the Martian analog sites. Here we use a Raman microscope and environmental cell to monitor the low-temperature (223 - 273 K) deliquescence (solid to aqueous phase transition) and efflorescence (aqueous to solid phase transition) of three hydration states of CaCl2 (dihydrate, tetrahydrate, hexahydrate). We have found that the deliquescence relative humidity (DRH) increases with increasing hydration state, which is an expected result. Average DRH values over the temperature range studied are 20.0 × 2.6% RH for the dihydrate, 31.8 × 6.3% RH for the tetrahydrate and 60.7 × 1.6% RH for the hexahydrate. Once the aqueous

  2. The solubility of quartz in aqueous sodium chloride solution at 350°C and 180 to 500 bars

    USGS Publications Warehouse

    Fournier, Robert O.; Rosenbauer, Robert J.; Bischoff, James L.

    1982-01-01

    The solubility of quartz in 2, 3, and 4 molal NaCl was measured at 350°C and pressures ranging from 180 to 500 bars. The molal solubility in each of the salt solutions is greater than that in pure water throughout the measured pressure range, with the ratio of solubility in NaCl solution to solubility in pure water decreasing as pressure is increased. The measured solubilities are significantly higher than solubilities calculated using a simple model in which the water activity in NaCl solutions decreases either in proportion to decreasing vapor pressure of the solution as salinity is increased or in proportion to decreasing mole fraction of water in the solvent.

  3. CONDENSED MATTER: STRUCTURE, MECHANICAL AND THERMAL PROPERTIES: Effect of Electrochemical Treatment in a Lithium Chloride Solution on Field Emission from Carbon Nanotubes

    NASA Astrophysics Data System (ADS)

    Wang, Qiang; Li, Chun; Yuan, Guang; Gu, Chang-Zhi

    2009-08-01

    Carbon nanotubes (CNTs) are electrochemically treated in a lithium chloride solution at a concentration 0.1 mol/L. The field emission properties of the CNTs are investigated at different temperatures before and after the electrochemical treatment. After treatment, the turn-on voltage to produce field emission current of 10 μA decreases from 4.2 kV to 2.7 kV and the field emission current increases distinctly, but the stability falls off. Based on the Fowler-Nordheim plot, the values of the work function for the CNTs are calculated, which reveals that work function decreases after the electrochemical treatment. These results are attributed to the decrease of the work function of the carbon nanotubes.

  4. An experimental study of zinc chloride speciation from 300 to 600 °C and 0.5 to 2.0 kbar in buffered hydrothermal solutions

    USGS Publications Warehouse

    Cygan, G.L.; Hemley, J.J.; d'Angelo, W. M.

    1994-01-01

    The solubility of sphalerite (ZnS) was measured in KCl-HCl-H2O solutions at 300-600??C and 0.5-2.0 kbar. The silicate assemblage K-feldspar-muscovite (or andalusite)-quartz was used to buffer the solution to acid conditions, resulting in the total solubility reaction 2K+ + KAl2AlSi3O10(OH)2 + 6SiO2 + ZnS + nCl- = ZnCln(2-n) + 3KAlSi3O8 + H2S. (muscovite) (quartz) (sphalerite) (K-feldspar) A computer retrieval technique was used to derive average chloride ligand numbers for chlorozinc species at 0.25-2.0 molal total chloride. This technique mathematically solves for the average ligand number using a series of pertinent chemical relations at P and T. Mono- and di-chlorozinc species were found to predominate throughout the pressure-temperature-composition range investigated. The logarithms of the first and second dissociation constants for ZnCl20 were evaluated over the P-T range; for example, at 1 kbar, the values -0.41 and -1.42 were computed for the logarithm of the first dissociation constant, while -7.62 and -10.57 were computed for the logarithm of the second dissociation constant, for 400 and 500??C, respectively. Results are compared to past studies conducted at subcritical conditions and differ in that we find no evidence for more highly coordinated chloro-zinc species except possibly for ZnCl3- at 600??C, 1 and 2 kbar. Our results are consistent with electrostatic theory, which favors lower charged to neutral molecules in low dielectric-constant media. ?? 1994.

  5. Adsorption of low concentration ceftazidime from aqueous solutions using impregnated activated carbon promoted by Iron, Copper and Aluminum

    NASA Astrophysics Data System (ADS)

    Hu, Xiang; Zhang, Hua; Sun, Zhirong

    2017-01-01

    In this paper, three impregnated activated carbon IAC (AC-Cu, AC-Fe, and AC-Al) promoted by Iron, Copper and Aluminum were used for adsorption of ceftazidime. Iron(III), Copper(II) and Aluminum(III) nitrate were used as an impregnant. The IACs were characterized by scanning electron microscope (SEM), Brunauer-Emmett-Teller (BET) surface area analyzer, Fourier transform infrared spectroscopy (FTIR) and X-ray Photoelectron Spectroscopy (XPS).The influence of factors, such as ion strength, pH, temperature, initial concentration, and concentration of natural organic matter organic matter on the adsorption process were studied. The adsorption kinetics and isotherms of ceftazidime were studied for the three IACs. The results showed that the adsorption was accurately represented by pseudo-second order model. Under different temperature, the maximum adsorption quantity of ceftazidime on AC-Cu calculated by pseudo-second order kinetic model were 200.0 mg g-1 (298 K), 196.1 mg g-1 (303 K) and 185.2 mg g-1 (308 K). It was much higher than that of AC-Fe and AC-Al. And the process was controlled by both film diffusion and intra particle mass transport. The results also showed that, the Freundlich and Temkin isotherm fit the adsorption well.

  6. Electrical Transport and Grain Growth in Solution-Cast, Chloride-Terminated Cadmium Selenide Nanocrystal Thin Films

    PubMed Central

    2015-01-01

    We report the evolution of electrical transport and grain size during the sintering of thin films spin-cast from soluble phosphine and amine-bound, chloride-terminated cadmium selenide nanocrystals. Sintering of the nanocrystals occurs in three distinct stages as the annealing temperature is increased: (1) reversible desorption of the organic ligands (≤150 °C), (2) irreversible particle fusion (200–300 °C), and (3) ripening of the grains to >5 nm domains (>200 °C). Grain growth occurs at 200 °C in films with 8 atom % Cl–, while films with 3 atom % Cl– resist growth until 300 °C. Fused nanocrystalline thin films (grain size = 4.5–5.5 nm) on thermally grown silicon dioxide gate dielectrics produce field-effect transistors with electron mobilities as high as 25 cm2/(Vs) and on/off ratios of 105 with less than 0.5 V hysteresis in threshold voltage without the addition of indium. PMID:24960255

  7. Thermogravimetric Thin Aqueous Film Corrosion Studies of Alloy 22; Calcium Chloride Solutions at 150C and Atmospheric Pressure

    SciTech Connect

    Hailey, P; Gdoowski, G

    2002-11-12

    The extent of reaction of alloy-22 with limited amounts of aqueous calcium chloride (CaCl{sub 2}) was investigated. Alloy-22 is a highly corrosion-resistant nickel-chromium-molybdenum-tungsten alloy. Specimens were polished to a mirror finish prior to aerosol salt deposition. An aqueous film was formed by deliquescence of deposited CaCl{sub 2} at 150 C and 22.5% relative humidity (RH). The reactant gas was a continuous flow of purified humidified laboratory air. The reaction progress as a function of time was continuously measured in-situ by a micro-balance. An initial weight gain due to deliquescence of the CaCl{sub 2} was observed. A steady weight loss was observed over the next 72 hours, after which no further weight change was observed. During this weight loss, white precipitates formed and the specimen's surface became visibly dry. The precipitate crystals were identified as Ca(OH){sub 2} by post-test Raman spectroscopy; however, energy dispersive X-ray spectroscopy indicated that there was a significant amount of chlorine contained in them.

  8. Hydrazino-methoxy-1,3,5-triazine Derivatives' Excellent Corrosion Organic Inhibitors of Steel in Acidic Chloride Solution.

    PubMed

    El-Faham, Ayman; Osman, Sameh M; Al-Lohedan, Hamad A; El-Mahdy, Gamal A

    2016-06-01

    The corrosion inhibition performance of 2-hydrazino-4,6-dimethoxy-1,3,5-tirazine (DMeHT), 2,4-dihydrazino-6-methoxy-1,3,5-triaizine (DHMeT), and 2,4,6-tridydrazino-1,3,5-triaizne (TH₃) on steel corrosion in acidic media was examined using electrochemical techniques. The results showed 2,4-Ddihydrazino-6-methoxy-1,3,5-triaizine (DHMeT) gave the best corrosion protection performance among the other hydrazino derivatives even at a low concentration of 25 ppm (95%). The number of hydrazino groups play an important role in the corrosion inhibition, where the two hydrazine groups increased the electrostatic interactions between the protonated tested compounds, the negatively charged steel surface resulted from the adsorption of the chloride anions, and the presence of the methoxy group made the compound more reliable for formation of film protection on the surface of steel through the lone pair of oxygen atoms. Electrochemical Impedance Spectroscopy (EIS) measurements suggested that the corrosion process of steel in presence of the hydrazino-s-triazine derivatives (TH₃, DMeHT and DHMeT) were being controlled by the charge transfer reaction. Polarization curves indicated that the examined TH₃, DMeHT and DHMeT behaved as mixed type inhibitors.

  9. Mechanism and toxicity research of benzalkonium chloride oxidation in aqueous solution by H2O2/Fe(2+) process.

    PubMed

    Zhang, Qian; Xia, Yu-Feng; Hong, Jun-Ming

    2016-09-01

    As widely used disinfectants, the pollution caused by benzalkonium chloride (BAC) has attracted a lot of attention in recent years. Since it is not suitable for biodegradation, BAC was degraded firstly by Fenton advanced oxidation technologies (AOTs) in this research to enhance the biodegradability of the pollutions. The result revealed that the optimal molar ratio of H2O2/Fe(2+) for BAC degradation was 10:1, and the COD removal rate was 32 %. To clarify the pathway of degradation, the technique of GC-MS was implemented herein to identify intermediates and the toxicity of those BAC intermediates were also novelty tested through microbial fuel cells (MFC). The findings indicated that ten transformation products including benzyl dimethyl amine and dodecane were formed during the H2O2/Fe(2+) processes, which means the degradation pathway of BAC was initiated both on the hydrophobic (alkyl chain) and hydrophilic (benzyl and ammonium moiety) region of the surfactant. The toxicity of BAC before and after treated by Fenton process was monitored through MFC system. The electricity generation was improved 337 % after BAC was treated by H2O2/Fe(2+) oxidation processes which indicated that the toxicity of those intermediates were much lower than BAC. The mechanism and toxicity research in this paper could provide the in-depth understanding to the pathway of BAC degradation and proved the possibility of AOTs for the pretreatment of a biodegradation process.

  10. Electrical transport and grain growth in solution-cast, chloride-terminated cadmium selenide nanocrystal thin films.

    PubMed

    Norman, Zachariah M; Anderson, Nicholas C; Owen, Jonathan S

    2014-07-22

    We report the evolution of electrical transport and grain size during the sintering of thin films spin-cast from soluble phosphine and amine-bound, chloride-terminated cadmium selenide nanocrystals. Sintering of the nanocrystals occurs in three distinct stages as the annealing temperature is increased: (1) reversible desorption of the organic ligands (≤150 °C), (2) irreversible particle fusion (200-300 °C), and (3) ripening of the grains to >5 nm domains (>200 °C). Grain growth occurs at 200 °C in films with 8 atom % Cl(-), while films with 3 atom % Cl(-) resist growth until 300 °C. Fused nanocrystalline thin films (grain size = 4.5-5.5 nm) on thermally grown silicon dioxide gate dielectrics produce field-effect transistors with electron mobilities as high as 25 cm(2)/(Vs) and on/off ratios of 10(5) with less than 0.5 V hysteresis in threshold voltage without the addition of indium.

  11. In-situ quantification of the effect of solute on the mobility, character and driving pressure of grain boundaries during recrystallization in aluminum alloys

    NASA Astrophysics Data System (ADS)

    Taheri, Mitra L.

    Aluminum alloys exhibit recrystallization kinetics that vary strongly with composition. The conventional understanding is that certain alloying elements, e.g. chromium, retard grain boundary motion due to the formation of tine dispersions of second phase particles, giving rise to particle drag of boundaries. There is countervailing evidence, however, that suggests that solute drag provides the stronger influence on the mobility of grain boundaries. This thesis presents new evidence of this pronounced effect of solute drag based on in-situ annealing (both SEM and TEM) and EBSD experiments involving recrystallization in aluminum alloys with varying composition in which individual boundaries move under the driving pressure of stored energy from prior plastic strain. This driving pressure is calculated both macroscopically (via Calorimetry, Microhardness) and microscopically (via Orientation Imaging Microscopy, Transmission Electron Microscopy). In all alloy compositions studied, a compensation effect is noted with respect to grain boundary mobility maxima for certain boundary types. A shift occurs in the misorientation associated with maximum mobility at 38--39°<111> observed at low temperatures, to misorientation axes towards <001>, <110> and <111> is seen in alloys when annealed at higher temperatures. A faceting/defaceting transition is also observed which is consistent with the changes in maximum mobility boundary type with increased temperature. These observations are supported by analysis of activation energy for boundary migration for each alloy. Evidence for irregular motion of boundaries from in-situ observations is discussed in reference to new theoretical results that suggest that boundaries migrating in the presence of solutes should move sporadically, provided that the length scale at which observations are made is small enough. Z-Contrast Imaging using a Scanning Transmission Electron Microscope coupled with TEM EDX analysis suggested variable Zr

  12. The effect of the electrochemical chloride extraction treatment on steel-reinforced mortar. Part II: Microstructural characterization

    SciTech Connect

    Marcotte, T.D.; Hansson, C.M.; Hope, B.B.

    1999-10-01

    A study has been made of the changes in cement composition and microstructures resulting from electrochemical chloride extraction applied to mortar samples in which the chlorides were added with the mixing water, ingressed by ponding with an NaCl solution, or both. After exposure for 1 year, specimens with and without chlorides were subjected to an electrochemical chloride extraction treatment. Microstructural analyses of fracture surfaces through the steel/mortar interface revealed a significant alteration of the cementitious phases. In untreated samples, calcium-silicon-rich phases consistent with Types I and II calcium silicate hydrate were observed. After the extraction treatment, these phases were not detectable and instead, sodium-rich, iron-rich, and calcium-aluminum-rich phases were observed.

  13. Removal of copper (II) from aqueous solutions by flotation using polyaluminum chloride silicate (PAX-XL60 S) as coagulant and carbonate ion as activator.

    PubMed

    Ghazy, S E; Mahmoud, I A; Ragab, A H

    2006-01-01

    Flotation is a separation technology for removing toxic heavy metal ions from aqueous solutions. Here a simple and rapid flotation procedure is presented for the removal of copper(II) from aqueous solutions. It is based on the use of polyaluminum chloride silicate (PAX-XL60 S) as coagulant and flocculent, carbonate ion as activator and oleic acid (HOL) as surfactant. Both ion and precipitate flotation are included depending on the solution pH. Ion and precipitate flotation in the aqueous HOL-PAX-XL60 S-Cu2+-CO3(2-) system gave powerful preferential removal of Cu2+ (F -100%) over the HOL-PAX-XL60 S-Cu2+ system containing no CO3(2+) ion (F approximately 86%). The role of CO3(2-) ion is also evident from decreasing the dose of PAX-XL60 S from 700 mg l(-1) to 200 mg l(-1). The other parameters, influencing the flotation process, namely: metal ion, surfactant and PAX-XL60 S concentrations, ionic strength, temperature and foreign ions were examined. Moreover, the procedure was successfully applied to recover Cu2+ ions from different volumes up to 11 and from natural water samples.

  14. RECOVERY OF ALUMINUM FROM FISSION PRODUCTS

    DOEpatents

    Blanco, R.E.; Higgins, I.R.

    1962-11-20

    A method is given for recovertng aluminum values from aqueous solutions containing said values together with fission products. A mixture of Fe/sub 2/O/ sub 3/ and MnO/sub 2/ is added to a solution containing aluminum and fission products. The resulting aluminum-containing supernatant is then separated from the fission product-bearing metal oxide precipitate and is contacted with a cation exchange resin. The aluminum sorbed on the resin is then eluted and recovered. (AEC)

  15. Corrosion behaviour of 316L stainless steel and anti-corrosion materials in a high acidified chloride solution

    NASA Astrophysics Data System (ADS)

    Jin, Z. H.; Ge, H. H.; Lin, W. W.; Zong, Y. W.; Liu, S. J.; Shi, J. M.

    2014-12-01

    The corrosion behaviour of a type 316L (UNS S31603) stainless steel (SS) expansion joint in a simulated leaching solution of sediment on blast furnace gas pipeline in a power plant is investigated by using dynamic potential polarization curves, electrochemical impedance spectroscopy (EIS), optical microscope, atomic force microscope (AFM) and Scan Kelvin Probe (SKP). Severe general corrosion accompanied by pitting corrosion occurs on the type 316L SS surface in this solution. As the immersion period increases, the charge transfer resistance Rct decreases, the dissolution rate accelerates, the surface roughness increases and the surface potential difference enhances significantly. Then eight corrosion-resistant materials are tested, the corrosion rates of type 254SMo SS, type 2507 SS and TA2 are relatively minor in the solution. The corrosion resistance properties of TA2 is most excellent, indicating it would be the superior material choice for blast furnace gas pipeline.

  16. Process development for the direct solvent extraction of nickel and cobalt from nitrate solution: aluminum, cobalt, and nickel separation using Cyanex 272

    NASA Astrophysics Data System (ADS)

    Ichlas, Zela T.; Ibana, Don C.

    2017-01-01

    A direct solvent extraction (DSX) process for purifying nickel and cobalt from the nitric acid leach solution of nickel laterite ores was conceived and experimentally probed. The proposed process consists of two solvent extraction (SX) steps but with only one extractant — bis(2,4,4-trimethylpentyl)phosphinic acid (Cyanex® 272) — used in both steps. The first extraction step involved the removal of aluminum and zinc, whereas the second extraction step involved the separation of cobalt along with manganese from nickel. The experimental results showed essentially quantitative removal of aluminum (>97%) and zinc (>99%) in a single extraction stage using 20vol% Cyanex 272 at pH 2.1. Some cobalt (32%) and manganese (55%) were co-extracted but were easily scrubbed out completely from the loaded organic phase using dilute sulfuric acid at pH ≤ 1.38. Cobalt and manganese in the first extraction raffinate were extracted completely in four extraction stages at staggered pH values of 4.0, 4.4, 4.5, and 4.0 in the first, second, third, and fourth stages, respectively, using also 20vol% Cyanex 272. A small amount of nickel (up to 6.6%) was co-extracted but was easily scrubbed out completely with dilute sulfuric acid at pH 2.0. A flow diagram showing the input and output conditions and the metals separated under the deduced optimum conditions is presented.

  17. Chloride Test

    MedlinePlus

    ... of the imbalance. In persons with too much base, urine chloride measurements can tell the healthcare practitioner whether the cause ... healthcare practitioner will look at whether the chloride measurement changes ... an acid-base imbalance and helps to guide treatment. ^ Back to ...

  18. Coexistence of iso-nonergodic laponite gel and glass in 1-methyl-3-octylimidazolium chloride ionic liquid solutions.

    PubMed

    Joshi, Nidhi; Rawat, Kamla; Bohidar, H B

    2014-06-12

    We report unique colloidal gel-glass coexistence in aqueous laponite dispersion (2% w/v) in the presence of 1-methyl-3-octylimidazolium chloride ionic liquid (IL, [C8mim][Cl], concentration 0.01 to 0.05% w/v), where both of the phases had identical nonergodicity and were dynamically interactive. With aging, the nascent heterogeneous dispersion exhibited spontaneous two-phase separation, and the time-dependent relative viscosity followed: η(r) = |ε|(-k) where ε = (t - t(g))/t(g) and t(g) is the time required for the system to get arrested, with k decreasing from 3.13 to 2.54 as the IL concentration was increased from 0 to 0.03% (w/v), implying slowing down of the arrest kinetics. This time was measured from viscosity and rheology studies, revealing the formation of IL-mediated finite size colloidal networks on a time scale of ~4 × 10(3) s, whereas the dispersion developed a large viscosity one decade in time later (~4 × 10(4) s). Homogeneous transparent upper phase was an entropic glass and exhibited substantial storage modulus gain (300-3000 Pa) with an increase in IL concentration (0 to 0.05% (w/v)). The translucent lower gel phase had a much higher storage modulus. Dynamic light scattering measured bimodal relaxation time of concentration fluctuations. The degree of nonergodicity in the two phases was approximately the same, implying laponite-IL cluster exchange across the interface (identical slow-mode diffusivity). In summary, IL-induced first-order phase separation in laponite dispersion produced a homogeneous colloidal gel coexisting with a glass not commonly observed in soft matter systems. This implied that the two phases were dynamically coupled on long time scales, whereas their short-time behavior was distinctively different.

  19. XAFS measurements on zinc chloride aqueous solutions from ambient to supercritical conditions using the diamond anvil cell

    USGS Publications Warehouse

    Mayanovic, Robert A.; Anderson, Alan J.; Bassett, William A.; Chou, I.-Ming

    1999-01-01

    The structure and bonding properties of metal complexes in subcritical and supercritical fluids are still largely unknown. Conventional high pressure and temperature cell designs impose considerable limitations on the pressure, temperature, and concentration of metal salts required for measurements on solutions under supercritical conditions. In this study, we demonstrate the first application of the diamond anvil cell, specially designed for x-ray absorption studies of first-row transition metal ions in supercritical fluids. Zn K-edge XAFS spectra were measured from aqueous solutions of 1-2m ZnCl2 and up to 6m NaCl, at temperatures ranging from 25-660 ??C and pressures up to 800 MPa. Our results indicate that the ZnCl42- complex is predominant in the 1m ZnCl2/6m NaCl solution, while ZnCl2(H2O)2 is similarly predominant in the 2m ZnCl2 solution, at all temperatures and pressures. The Zn-Cl bond length of both types of chlorozinc(II) complexes was found to decrease at a rate of about 0.01 A??/100 ??C.

  20. Growth, Water Content, and Solute Accumulation of Two Tobacco Cell Lines Cultured on Sodium Chloride, Dextran, and Polyethylene Glycol 1

    PubMed Central

    Heyser, James W.; Nabors, Murray W.

    1981-01-01

    Simulated drought tolerance was compared for an NaCl-adapted and a nonadapted cell line of tobacco (Nicotiana tabacum var. Samsum) to determine the relationship of salt and drought tolerances. The osmotic adjustment and growth of these two lines was followed when cultured on solid media which contained isosmotic concentrations of NaCl, KCl, polyethylene glycol (PEG) or dextran. One line was adapted to growth on 130 millimolar NaCl, but the other was not. The growth of NaCl-adapted and nonadapted cell lines was equally inhibited (61 per cent of control) by 130 millimolar NaCl. Growth inhibition was greater on PEG or dextran than on NaCl. Growth ceased on the second passage of dextran for the nonadapted cells, while the NaCl-adapted cells grew slowly for four passages on dextran. Water contents for both cell lines were 95 per cent on NaCl or KCl and 70 to 88 per cent on PEG 1540 or 4000 or dextran after the second passage on these media. On dextran or PEG 4000, 46 to 89 per cent of the cellular osmotic potential was produced by the solutes initially present in the medium. Similarly, on NaCl, almost 100 per cent was attributable to solutes in the medium. It was concluded that cells grown on the nonpenetrating solutes had a more negative osmotic potential than those grown in the absence of added solute due to partial dehydration, greater uptake of external ions, and possibly the production of unidentified osmotica. Adjustment to growth on penetrating solutes may have enabled the adapted line to overcome the osmotic stress produced by nonpenetrating dextran. PMID:16662125

  1. Corrosion Behavior of Novel Al-Al2O3 Composites in Aerated 3.5% Chloride Solution

    NASA Astrophysics Data System (ADS)

    Acevedo-Hurtado, P. O.; Sundaram, P. A.

    2017-01-01

    The corrosion behavior of novel Al-Al2O3 MMCs was evaluated in aerated 3.5% NaCl solution through potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). These materials corrode almost spontaneously by pitting in aerated 3.5% NaCl solution. Observations indicate that intermetallic particles in these composites appear to play an important role in this pitting corrosion behavior. Addition of Al2O3 particles to the base alloys did not appear to increase their corrosion resistance significantly, although corrosion rate was affected by these reinforcement particles. In cyclic polarization experiments, the small difference between the pitting potentials and the repassivation potentials for these MMCs indicated their low resistance to pitting corrosion. EIS measurements indicate adsorption/diffusion phenomena at the interface of the composites. Electrically equivalent circuits are proposed to describe and substantiate the corrosion processes occurring in these materials.

  2. Study of caffeine as corrosion inhibitors of carbon steel in chloride solution containing hydrogen sulfide using electrochemical impedance spectroscopy (EIS)

    NASA Astrophysics Data System (ADS)

    Solehudin, Agus; Berman, Ega Taqwali; Nurdin, Isdiriayani

    2015-09-01

    The corrosion behaviour of steel surface in the absence and presence of caffeine in 3.5% NaCl solution containing dissolved H2S gas is studied using electrochemical impedance spectroscopy (EIS). The experimental results of carbon steel corrosion in 3.5% NaCl solution containing 500 mg/l H2S at different caffeine concentrations showed that corrosion rate of carbon steel decreases with increasing of caffeine concentrations from 0 to 0,1 mmol/l. Whereas, the corrosion rate increase with increasing of caffeine concentrations from 1 to 10 mmol/l. It is clear that no inhibition efficiency increases with increasing inhibitor concentration. The optimum value of inhibition efficiency was 90% at a caffeine concentration of 0.1 mmol/l. This suggests that caffeine's performance as a corrosion inhibitor is more effective at a concentration of 0.1 mmol/l.

  3. Effect of the cation model on the equilibrium structure of poly-L-glutamate in aqueous sodium chloride solution

    NASA Astrophysics Data System (ADS)

    Marchand, Gabriel; Soetens, Jean-Christophe; Jacquemin, Denis; Bopp, Philippe A.

    2015-12-01

    We demonstrate that different sets of Lennard-Jones parameters proposed for the Na+ ion, in conjunction with the empirical combining rules routinely used in simulation packages, can lead to essentially different equilibrium structures for a deprotonated poly-L-glutamic acid molecule (poly-L-glutamate) dissolved in a 0.3M aqueous NaCl solution. It is, however, difficult to discriminate a priori between these model potentials; when investigating the structure of the Na+-solvation shell in bulk NaCl solution, all parameter sets lead to radial distribution functions and solvation numbers in broad agreement with the available experimental data. We do not find any such dependency of the equilibrium structure on the parameters associated with the Cl- ion. This work does not aim at recommending a particular set of parameters for any particular purpose. Instead, it stresses the model dependence of simulation results for complex systems such as biomolecules in solution and thus the difficulties if simulations are to be used for unbiased predictions, or to discriminate between contradictory experiments. However, this opens the possibility of validating a model specifically in view of analyzing experimental data believed to be reliable.

  4. Electrochemical Studies in Aluminum Chloride Melts

    DTIC Science & Technology

    1976-07-31

    aid. it ReCOAeWy and Idmntli by block tnm&.C) molten salts ; sodium tetrachioroaluminate; sulfur; molybdenoat; chal cogenides/ 20 ABSTRACT (Continue an...the Seller Research Laboratory at the United States Air Force Academy. Dis- cussions were held relating to both the sodium tetrachloroaluminate system... Sodium Tetrachloroaluminate", J. Org. Chem., 39, 2416 (1974). H. Lloyd Jones and R. A. Osteryoung, "Organic Reactions in Molten Tetrachloro

  5. Organic Electrochemistry in Aluminum Chloride Melts.

    DTIC Science & Technology

    1976-08-15

    CLASS. (.5 Uit• “P.’U (21F,n~!ye~ t . _ _ _ _ _ _ _ _ _ _ _ _I .~~. cY~ t 7~ .3~ ~‘l+g 7~ \\ ii.. kt~~I1ICAY* ONYCO ~ $GRA D*$G IU OIITRIIUTIOM STATEMENT (.1...DOCUMENTATION PAGE 8aFO CO~~~~~~~ NC~ PORM i. REPORT NUNSER 3. GOVT ACCIIZION NO 3. RtC,PIENt ’i C A T A ~ O~~ NUN.LR TIY ~.E (~~~~3~.AtIaS.) I YVPE OF...REPORT I PERIOD COVERED Final- 1 October 1972- • t ~~ ‘~~~~ _ ( Organic Electrochemistry in Al uminum .-~~ 30 May 1976 ~ L ~~~~~~~~~~~~~~~ I •. •i~ ,o

  6. Effects of postexsanguination vascular infusion of cattle with a solution of saccharides, sodium chloride, and phosphates or with calcium chloride on quality and sensory traits of steaks and ground beef.

    PubMed

    Dikeman, M E; Hunt, M C; Addist, P B; Schoenbeck, H J; Pullen, M; Katsanidis, E; Yancey, E J

    2003-01-01

    Grain-finished Hereford x Angus steers (n = 36) were assigned to one of three treatmentgroups. Immediately after jugular exsanguination, 12 steers were infused at 10% of live weight via the left carotid artery with a solution developed by MPSC, Inc. (St. Paul, MN) consisting of 98.52% water, 0.97% saccharides, 0.23% sodium chloride, and 0.28% phosphate blend (MPSC); 12 steers were infused at 10% of live weight with 0.30 M CaCl2 (CaCl2); and 12 steers were exsanguinated conventionally and served as noninfused controls (CON). Declines in pH for three muscles were measured. CaCl2-infused carcasses exhibited extensive muscle contraction at the time of cooler entry. Carcasses were graded at 24 h postmortem and fabricated at 48 h postmortem. Longissimus lumborum (LL), semitendinosus (ST), and quadriceps femoris (QF) muscles were removed, vacuum packaged, and stored at 2 degrees C until 14 d postmortem. Then, 2.54-cm-thick steaks were cut from the LL and ST for shear force and sensory evaluations. Ground beef was formulated from the QF to contain 20% fat. Steers infused with MPSC and CaCl2 had 4.0 and 2.3% higher dressing percentage points, respectively, than CON steers. Calcium concentrations of the LL muscle for CaCl2- and MPSC-infused carcasses, as well as the CON carcasses, were 892.0, 158.9, and 216.6 ppm, respectively. For the TB and longissimus thoracis muscles, pH decline was more rapid for CaCl2- and MPSC-infused carcasses than for CON carcasses, but there were no differences in 24-h pH. Warner-Bratzler shear force values were much higher (P < 0.05), and descriptive attribute sensory panel tenderness scores much lower (P < 0.05), for the LL from CaCl2-infused carcasses than for MPSC-infused and CON carcasses. Flavor intensity of the LL of CaCl2-infused carcasses was reduced (P < 0.05); however, overall tenderness and flavor of the ST were unaffected (P > 0.05) by CaCl2 infusion. Beef flavor identification, brown-roasted flavor, and bloody/serumy flavor were

  7. First-principles study on stability of transition metal solutes in aluminum by analyzing the underlying forces

    NASA Astrophysics Data System (ADS)

    Liu, Wei; Xu, Yichun; Li, Xiangyan; Wu, Xuebang; Liu, C. S.; Liang, Yunfeng; Wang, Zhiguang

    2015-05-01

    Although there have been some investigations on behaviors of solutes in metals under strain, the underlying mechanism of how strain changes the stability of a solute is still unknown. To gain such knowledge, first-principles calculations are performed on substitution energy of transition metal solutes in fcc Al host under rhombohedral strain (RS). Our results show that under RS, substitution energy decreases linearly with the increase of outermost d radius rd of the solute due to Pauli repulsion. The screened Coulomb interaction increases or decreases the substitution energy of a solute on condition that its Pauling electronegativity scale ϕ P is less or greater than that of Al under RS. This paper verifies a linear relation of substitution energy change versus rd and ϕ P under RS, which might be instructive for composition design of long life alloys serving in high stress condition.

  8. First-principles study on stability of transition metal solutes in aluminum by analyzing the underlying forces

    SciTech Connect

    Liu, Wei; Xu, Yichun; Li, Xiangyan; Wu, Xuebang Liu, C. S.; Liang, Yunfeng; Wang, Zhiguang

    2015-05-07

    Although there have been some investigations on behaviors of solutes in metals under strain, the underlying mechanism of how strain changes the stability of a solute is still unknown. To gain such knowledge, first-principles calculations are performed on substitution energy of transition metal solutes in fcc Al host under rhombohedral strain (RS). Our results show that under RS, substitution energy decreases linearly with the increase of outermost d radius r{sub d} of the solute due to Pauli repulsion. The screened Coulomb interaction increases or decreases the substitution energy of a solute on condition that its Pauling electronegativity scale ϕ{sub P} is less or greater than that of Al under RS. This paper verifies a linear relation of substitution energy change versus r{sub d} and ϕ{sub P} under RS, which might be instructive for composition design of long life alloys serving in high stress condition.

  9. Time exposure studies on stress corrosion cracking of aluminum 2014-T6, aluminum 7075-T651, and titanium 6Al-4V

    NASA Technical Reports Server (NTRS)

    Terrell, J.

    1972-01-01

    The effect of a constant applied stress in crack initiation of aluminum 2014-T6, 7075-T651 and titanium 6A1-4V has been investigated. Aluminum c-ring specimens (1-inch diameter) and u-band titanium samples were exposed continuously to a 3.5% NaCl solution (pH 6) and organic fluids of ethyl, methyl, and iso-propyl alcohol (reagent purity). Corrosive action was observed to begin during the first and second day of constant exposure as evidenced by accumulation of hydrogen bubbles on the surface of stressed aluminum samples. However, a similar observation was not noted for titanium stressed specimens. Results of this investigation seems to suggest that aluminum 2014-T6, aluminum 7075-T651 are susceptible to stress corrosion cracking in chloride solution (NaCl); while they (both alloys) seem to resist stress corrosion cracking in methyl alcohol, ethyl alcohol, iso-propyl alcohol, and demineralized distilled water. Titanium 6A1-4V showed some evidence of susceptibility to SCC in methanol, while no such susceptibility was exhibited in ethanol, iso-propyl alcohol and demineralized distilled water.

  10. EVALUATION OF LOW TEMPERATURE ALUMINUM DISSOLUTION IN TANK 51

    SciTech Connect

    Pike, J

    2008-09-04

    loss from a quiescent tank; and an evaluation of the aluminum dissolution rate model and actual dissolution rate. LTAD was successfully completed in Tank 51 with minimal waste tank changes. The following general conclusions may be drawn about the LTAD process: (1) Dissolution at about 60 C for 46 days dissolved 64% of the aluminum from the sludge slurry. (2) The aluminum-laden leach solution decanted to Tank 11 can be blended with a wide variety of supernates without risk of precipitating the dissolved aluminum based on thermodynamic chemical equilibrium models. (3) Uranium and plutonium leached into solution without corresponding leaching of iron or metal other than aluminum, but the total mass leached was a small fraction of the total uranium and plutonium in the sludge. (4) The concentration of uranium and plutonium in the leach solution was indistinguishable from other tank farm supernates, thus, the leach solutions can be managed relative to the risk of criticality like any other supernate. (5) A small amount of mercury leached into solution from the sludge causing the liquid phase concentration to increase 6 to 10 fold, which is consistent with the 4 to 14 fold increase observed during the 1982 aluminum dissolution demonstration. (6) Chromium did not dissolve during LTAD. (7) Chloride concentration increased in the liquid phase during LTAD due to chloride contamination in the 50% sodium hydroxide solution. (8) The rate of heat loss from Tank 51 at temperatures above 45 C appeared linear and predictable at 8E+7 cal/hr. (9) The rate of heat transfer from Tank 51 did not follow a simplified bulk heat transfer model. (10) Prediction of the aluminum dissolution rate was prone to error due to a lack of active specific surface area data of sludge particles. (11) The higher than expected dissolution rate during LTAD was likely due to smaller than expected particle sizes of most of the sludge particles. While evaluating the LTAD process, the dissolved salt solution from

  11. Electrical and Surface Morphology of Polyvinylchloride Composites Filled with Aluminum Powder

    SciTech Connect

    Singh, Dolly; Kishore, Sangeeta; Singh, N. L.

    2011-07-15

    In this work, the electrical and surface morphology of polyvinyl chloride (PVC) composites filled with different concentration of aluminum powder varying from 0 to 40 wt.% have been prepared by solution costing method. The electrical conductivity of these composites were investigated in the frequency range 100 Hz-10 MHz at room temperature. The conductivity of the composites system exhibited a strong frequency dependence particularly in the vicinity of percolation threshold (20 wt.%). It was observed that the electrical conductivity gradually increased with filler concentration and frequency and explained in terms of hopping conduction mechanism. The electrical conductivity of the composites obeys universal power law (i.e. {sigma} = Af{sup n}), where, n is power exponent. The scanning electron microscope (SEM) micrographs indicate the agglomeration of aluminum particles dispersed within the PVC at the higher aluminum concentration, yielding a conductive path through the composites. It is also corroborated with electrical conductivity result.

  12. Adsorption equilibria between liposome membrane formed of phosphatidylcholine and aqueous sodium chloride solution as a function of pH.

    PubMed

    Kotyńska, J; Figaszewski, Z A

    2005-12-30

    The effect has been studied of the adsorption of ions (H(+), Na(+), OH(-), Cl(-)) which are present in solution upon the electric charge of the liposome membrane formed of phosphatidylcholine (PC). The surface charge density of the membrane was determined as a function of pH and electrolyte concentration from electrophoretic mobility measurements. The measurements were carried out by the laser-Doppler microelectrophoresis method. A four-equilibria model has been proposed to describe the phenomena occurring on the membrane surface. The equilibria in which the adsorption of other ions on the liposome membrane surface was involved were assumed to exist beside the equilibria in which the H(+) and OH(-) ions were engaged. The idea was confirmed by mathematical calculations. Association constants of the liposome membrane surface with ions of solution (K(AH), K(ANa), K(BOH), K(BCl)) were determined. The proposed model has been proved to be correct by comparing the resulting theoretic charge variation curves of the lecithin membrane with the experimental data.

  13. Effect of sodium chloride on solute-solvent interactions in aqueous polyethylene glycol-sodium sulfate two-phase systems.

    PubMed

    da Silva, Nuno R; Ferreira, Luisa A; Madeira, Pedro P; Teixeira, José A; Uversky, Vladimir N; Zaslavsky, Boris Y

    2015-12-18

    Partition behavior of eight small organic compounds and six proteins was examined in poly(ethylene glycol)-8000-sodium sulfate aqueous two-phase systems containing 0.215M NaCl and 0.5M osmolyte (sorbitol, sucrose, TMAO) and poly(ethylene glycol)-10000-sodium sulfate-0.215M NaCl system, all in 0.01M sodium phosphate buffer, pH 6.8. The differences between the solvent properties of the coexisting phases (solvent dipolarity/polarizability, hydrogen bond donor acidity, and hydrogen bond acceptor basicity) were characterized with solvatochromic dyes using the solvatochromic comparison method. Differences between the electrostatic properties of the phases were determined by analysis of partitioning of sodium salts of dinitrophenylated (DNP-) amino acids with aliphatic alkyl side-chain. The partition coefficients of all compounds examined (including proteins) were described in terms of solute-solvent interactions. The results obtained in the study show that solute-solvent interactions of nonionic organic compounds and proteins in polyethylene glycol-sodium sulfate aqueous two-phase system change in the presence of NaCl additive.

  14. Probing liquation cracking and solidification through modeling of momentum, heat, and solute transport during welding of aluminum alloys

    NASA Astrophysics Data System (ADS)

    Mishra, S.; Chakraborty, S.; DebRoy, T.

    2005-05-01

    A transport phenomena-based mathematical model is developed to understand liquation cracking in weldments during fusion welding. Equations of conservation of mass, momentum, heat, and solute transport are numerically solved considering nonequilibrium solidification and filler metal addition to determine the solid and liquid phase fractions in the solidifying region and the solute distribution in the weld pool. An effective partition coefficient that considers the local interface velocity and the undercooling is used to simulate solidification during welding. The calculations show that convection plays a dominant role in the solute transport inside the weld pool. The predicted weld-metal solute content agreed well with the independent experimental observations. The liquation cracking susceptibility in Al-Cu alloy weldments could be reliably predicted by the model based on the computed solidifying weld-metal composition and solid fraction considering nonequilibrium solidification.

  15. Determination of Chloride in Hydraulic Fluids.

    DTIC Science & Technology

    1986-10-01

    chloride stock solution (1000 mg/L) was prepared by dissolv- ing sodium chloride in deionized distilled water. A 5M sodium nitrate solu- tion was used as...electrode as the reference electrode. Calibration curves were prepared by measuring the potentials (millivolts) of standard chloride solution (1, 10, 100...Therefore, it is recommended that only 10% (v/v) hydraulic fluid ( ehtylene glycol) solutions be used for analysis. The electrode must not stay in the

  16. 21 CFR 184.1138 - Ammonium chloride.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    .... No. 12125-02-9) is produced by the reaction of sodium chloride and an ammonium salt in solution. The less soluble sodium salt separates out at elevated temperatures, and ammonium chloride is recovered... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Ammonium chloride. 184.1138 Section 184.1138...

  17. 21 CFR 184.1138 - Ammonium chloride.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    .... No. 12125-02-9) is produced by the reaction of sodium chloride and an ammonium salt in solution. The less soluble sodium salt separates out at elevated temperatures, and ammonium chloride is recovered... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Ammonium chloride. 184.1138 Section 184.1138...

  18. 21 CFR 184.1138 - Ammonium chloride.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    .... No. 12125-02-9) is produced by the reaction of sodium chloride and an ammonium salt in solution. The less soluble sodium salt separates out at elevated temperatures, and ammonium chloride is recovered... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Ammonium chloride. 184.1138 Section 184.1138...

  19. 21 CFR 184.1138 - Ammonium chloride.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    .... No. 12125-02-9) is produced by the reaction of sodium chloride and an ammonium salt in solution. The less soluble sodium salt separates out at elevated temperatures, and ammonium chloride is recovered... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Ammonium chloride. 184.1138 Section 184.1138...

  20. Moessbauer spectroscopy study on the corrosion resistance of plasma nitrided ASTM F138 stainless steel in chloride solution

    SciTech Connect

    Souza, S.D. de; Olzon-Dionysio, M.; Basso, R.L.O.; Souza, S. de

    2010-10-15

    Plasma nitriding of ASTM F138 stainless steel samples has been carried out using dc glow discharge under 80% H{sub 2}-20% N{sub 2} gas mixture, at 673 K, and 2, 4, and 7 h time intervals, in order to investigate the influence of treatment time on the microstructure and the corrosion resistance properties. The samples were characterized by scanning electron microscopy, glancing angle X-ray diffraction and conversion electron Moessbauer spectroscopy, besides electrochemical tests in NaCl aerated solution. A modified layer of about 6 {mu}m was observed for all the nitrided samples, independent of nitriding time. The X-ray diffraction analysis shows broad {gamma}{sub N} phase peaks, signifying a great degree of nitrogen supersaturation. Besides {gamma}{sub N,} the Moessbauer spectroscopy results indicated the occurrence of {gamma}' and {epsilon} phases, as well as some other less important phases. Corrosion measurements demonstrate that the plasma nitriding time affects the corrosion resistance and the best performance is reached at 4 h treatment. It seems that the {epsilon}/{gamma}' fraction ratio plays an important role on the resistance corrosion. Additionally, the Moessbauer spectroscopy was decisive in this study, since it was able to identify and quantify the iron phases that influence the corrosion resistance of plasma nitrided ASTM F138 samples.

  1. Dissolution and Separation of Aluminum and Aluminosilicates

    SciTech Connect

    McFarlane, Joanna; Benker, Dennis; DePaoli, David W.; Felker, Leslie Kevin; Mattus, Catherine H.

    2015-12-19

    The selection of an aluminum alloy for target irradiation affects post-irradiation target dissolution and separations. Recent tests with aluminum alloy 6061 yielded greater than expected precipitation in the dissolver, forming up to 10 wt.% solids of aluminum hydroxides and aluminosilicates. Aluminosilicate dissolution presents challenges in a number of different areas, metals extraction from minerals, flyash treatment, and separations from aluminum alloys. We present experimental work that attempts to maximize dissolution of aluminum metal, along with silicon, magnesium, and copper impurities, through control of temperature, the rate of reagent addition, and incubation time. Aluminum phase transformations have been identified as a function of time and temperature, using X-ray diffraction. Solutions have been analyzed using wet chemical methods and X-ray fluorescence. Our data have been compared with published calculations of aluminum phase diagrams. Approaches are given to enhance the dissolution of aluminum and aluminosilicate phases in caustic solution.

  2. Dissolution and Separation of Aluminum and Aluminosilicates

    DOE PAGES

    McFarlane, Joanna; Benker, Dennis; DePaoli, David W.; ...

    2015-12-19

    The selection of an aluminum alloy for target irradiation affects post-irradiation target dissolution and separations. Recent tests with aluminum alloy 6061 yielded greater than expected precipitation in the dissolver, forming up to 10 wt.% solids of aluminum hydroxides and aluminosilicates. Aluminosilicate dissolution presents challenges in a number of different areas, metals extraction from minerals, flyash treatment, and separations from aluminum alloys. We present experimental work that attempts to maximize dissolution of aluminum metal, along with silicon, magnesium, and copper impurities, through control of temperature, the rate of reagent addition, and incubation time. Aluminum phase transformations have been identified as amore » function of time and temperature, using X-ray diffraction. Solutions have been analyzed using wet chemical methods and X-ray fluorescence. Our data have been compared with published calculations of aluminum phase diagrams. Approaches are given to enhance the dissolution of aluminum and aluminosilicate phases in caustic solution.« less

  3. Effects of Cooling Rate and Solute Content on the Grain Refinement of Mg-Gd-Y Alloys by Aluminum

    NASA Astrophysics Data System (ADS)

    Dai, Jichun; Easton, Mark A.; Zhang, Mingxing; Qiu, Dong; Xiong, Xiangyuan; Liu, Wencai; Wu, Guohua

    2014-09-01

    The effect of Al additions on grain refinement of Mg-Gd-Y alloys with different solute contents at different cooling rates has been investigated. For all alloys, significant grain refinement was due to the formation of Al2(Gd x Y1- x ) nucleant particles. The number density and size distribution of Al2(Gd x Y1- x ) were affected by both solute content and the cooling rate. Grain sizes ( d gs) of Mg-Gd-Y base alloys and of Mg-Gd-Y-Al alloys were related to solute content (defined by the growth restriction factor, Q), cooling rate (), and area number density ( ρ ns) and size ( d p) of nucleant particles that can be activated. It is found that grain sizes of Mg-Gd-Y base alloys follow the relationship , while grain sizes of Al-refined samples follow the relationship , where a, b, a', and b' were constants. In addition, the grain refinement effect of Al additions was more susceptible to solute content and the cooling rate than that of Zr which is regarded as the most efficient grain refiner for Mg alloys.

  4. Totally solution-processed CuInS2 solar cells based on chloride inks: reduced metastable phases and improved current density

    NASA Astrophysics Data System (ADS)

    Dehghani, Mehdi; Behjat, Abbas; Tajabadi, Fariba; Taghavinia, Nima

    2015-03-01

    Planar superstrate CuInS2 (CIS) solar cell devices are fabricated using totally solution-processed deposition methods. These Cd-free devices are structured by FTO/TiO2/In2S3/CIS/carbon, where TiO2 and In2S3 are deposited by spray pyrolysis, and a CIS film is deposited using spin-coating followed by annealing at 250 °C. The pasted carbon layer is utilized as the anode. No further sulfurization or selenization is employed. The Cu/In ratio in the ink is found as a critical factor affecting the morphology and crystallinity of the film as well as the photovoltaic performance of the device. An optimum Cu/In = 1.05 results in large-grain films with sharp diffraction peaks and, subsequently, optimal series resistance and shunt conductance. It is also found that the chloride-based ink results in CIS films with considerably reduced metastable phases, compared to the conventional acetate-based inks. A current density of 23.6 mA cm-2 is obtained for the best devices, leading to a conversion efficiency of 4.1%.

  5. The study of the varying characteristics of cathodic regions for defective coating in 3.5% sodium chloride solution by EIS and WBE

    NASA Astrophysics Data System (ADS)

    Wang, Haijie; Wang, Jia; Wang, Wei; Zhang, Wei

    2015-04-01

    The current distributions over carbon steel under iron red alkyd primer exposed to 3.5% sodium chloride solution were mapped using the wire beam electrode (WBE). The electrochemical impedance spectroscopy (EIS) of the WBE was carried out to analyze the performance of coating delamination and corrosion behavior of carbon steel beneath defective coating. The EIS data revealed that protective capability of coating decreased with immersion time and the degree of cathodic delamination showed a rapid rise. The current density distribution of WBE indicated that cathodic sites was located at the defect at the beginning of immersion and gradually spread into the intact coating. The cathodic regions were distinguished from the anodic area and distributed over the WBE. The changes of cathodic sites could reflect the deterioration process of defective coating. The cathodic area ratio was a more useful parameter than the cathodic delamination degree to evaluate the coating cathodic delamination. The polarity reversals of electrodes at the defect and beneath coating were observed. A simple discussion of relationship between the blister and the polarity reversal was made from a standpoint of electrochemical distribution. WBE method was able to map and record the changes of local cathodic sites beneath defective coating in real time, which could provide more detailed information about the local degradation of coating.

  6. Extraction Equilibrium of Mn2+, Ca2+, and Mg2+ from Chloride Solutions by Di(2-ethylhexyl)phosphoric Acid Dissolved in Kerosene

    NASA Astrophysics Data System (ADS)

    Zhang, Chuanfu; Cao, Wenxin; Zhan, Jing; Ding, Fenghua; Hwang, Jiann-Yang

    2015-05-01

    The presence of calcium and magnesium affects the purity of the final product MnCl2 in hydrometallurgical treatment processes. The solvent extraction method can be used to separate Ca2+ and Mg2+ from Mn2+ solutions containing impurity ions such as Ca2+ and Mg2+. This article aims to investigate the single-stage extraction equilibrium of Ca2+, Mg2+, and Mn2+ in chloride medium using di(2-ethylhexyl)phosphoric acid in kerosene (O:A = 1:1). The results show that the pH0.5 values are 1.11, 1.56, and 2.18 for Ca2+, Mn2+, and Mg2+, respectively. The mechanism of extraction and stoichiometries of metal-containing extracted species were illustrated based on a slope analysis. The composition of the extracted species in the organic phase is proposed to be MnR2·R2H2, CaR2·R2H2, and MgR2·(R2H2)2, respectively.

  7. Hydrolysis of insoluble cellulose to glucose catalyzed by cellulase-containing liposomes in an aqueous solution of 1-butyl-3-methylimidazolium chloride.

    PubMed

    Yoshimoto, Makoto; Tanimura, Kazuhiko; Tokunaga, Kazuki; Kamimura, Akio

    2013-01-01

    The liposome containing cellulase from Trichoderma viride was prepared under the condition that an appreciable amount of cellulase was incorporated in lipid membranes. The liposomal cellulase and free enzyme were examined in their hydrolytic activities to insoluble cellulose powder CC31 in the acetate buffer solution (pH 4.8) of 15 w/w% [Bmim][Cl] (1-butyl-3-methylimidazolium chloride). The mean diameter and size distribution of cellulase-containing liposome were practically unchanged under the above condition. The free cellulase was deactivated more rapidly than the liposomal cellulase in catalyzing the hydrolysis of 2.0 g/l CC31 at 45°C in the presence of [Bmim][Cl] for 48 h. The activities of liposomal and free cellulase to cellobiose as soluble substrate were less susceptible to [Bmim][Cl] than their cellulolytic activities to CC31, meaning that β-glucosidase is relatively stable among the three enzyme components of cellulase. The rate of glucose production could be appreciably improved by the pretreatment of CC31 with [Bmim][Cl] alone at 120°C for 30 min followed by the liposomal cellulase-catalyzed hydrolysis of the substrate at 45°C at the [Bmim][Cl] concentration of 15 w/w%.

  8. [Sodium chloride 0.9%: nephrotoxic crystalloid?].

    PubMed

    Dombre, Vincent; De Seigneux, Sophie; Schiffer, Eduardo

    2016-02-03

    Sodium chloride 0.9%, often incorrectly called physiological saline, contains higher concentration of chloride compared to plasma. It is known that the administration of sodium chloride 0.9% can cause hyperchloremic metabolic acidosis in a reproducible manner. The elevated chloride concentration in 0.9% NaCl solution can also adversely affect renal perfusion. This effect is thought to be induced by hyperchloremia that causes renal artery vasoconstriction. For these reasons, the use of 0.9% NaCl solution is raising attention and some would advocate the use of a more "physiological" solution, such as balanced solutions that contain a level of chloride closer to that of plasma. Few prospective, randomized, controlled trials are available today and most were done in a perioperative setting. Some studies suggest that the chloride excess in 0.9% NaCl solution could have clinical consequences; however, this remains to be established by quality randomized controlled trials.

  9. REMOVAL OF ALUMINUM COATINGS

    DOEpatents

    Peterson, J.H.

    1959-08-25

    A process is presented for dissolving aluminum jackets from uranium fuel elements without attack of the uranium in a boiling nitric acid-mercuric nitrate solution containing up to 50% by weight of nitrtc acid and mercuric nitrate in a concentration of between 0.05 and 1% by weight.

  10. Antibacterial activity of silver nanoparticles obtained by pulsed laser ablation in pure water and in chloride solution

    PubMed Central

    Perito, Brunella; Giorgetti, Emilia; Marsili, Paolo

    2016-01-01

    Summary Silver nanoparticles (AgNPs) have increasingly gained importance as antibacterial agents with applications in several fields due to their strong, broad-range antimicrobial properties. AgNP synthesis by pulsed laser ablation in liquid (PLAL) permits the preparation of stable Ag colloids in pure solvents without capping or stabilizing agents, producing AgNPs more suitable for biomedical applications than those prepared with common, wet chemical preparation techniques. To date, only a few investigations into the antimicrobial effect of AgNPs produced by PLAL have been performed. These have mainly been performed by ablation in water with nanosecond pulse widths. We previously observed a strong surface-enhanced Raman scattering (SERS) signal from such AgNPs by “activating” the NP surface by the addition of a small quantity of LiCl to the colloid. Such surface effects could also influence the antimicrobial activity of the NPs. Their activity, on the other hand, could also be affected by other parameters linked to the ablation conditions, such as the pulse width. The antibacterial activity of AgNPs was evaluated for NPs obtained either by nanosecond (ns) or picosecond (ps) PLAL using a 1064 nm ablation wavelength, in pure water or in LiCl aqueous solution, with Escherichia coli and Bacillus subtilis as references for Gram-negative and Gram-positive bacteria, respectively. In all cases, AgNPs with an average diameter less than 10 nm were obtained, which has been shown in previous works to be the most effective size for bactericidal activity. The measured zeta-potential values were very negative, indicating excellent long-term colloidal stability. Antibacterial activity was observed against both microorganisms for the four AgNP formulations, but the ps-ablated nanoparticles were shown to more effectively inhibit the growth of both microorganisms. Moreover, LiCl modified AgNPs were the most effective, showing minimum inhibitory concentration (MIC) values in a

  11. Ion association of dilute aqueous potassium chloride and potassium hydroxide solutions to 600°C and 300 MPa determined by electrical conductance measurements

    NASA Astrophysics Data System (ADS)

    Ho, Patience C.; Palmer, Donald A.

    1997-08-01

    The limiting molar conductances ( Λ0) and ion association constants of dilute (<0.01 mol · kg -1) aqueous potassium chloride and hydroxide solutions were determined by electrical conductance measurements from 200 to 600°C and from 100 to 600°C, respectively, and pressures up to 300 MPa. The limiting molar conductances of KOH (aq) increase with increasing temperature up to 300°C and decreasing density. Above 400°C and densities between 0.8 and 0.4 g · cm -3 for KCl (aq) and between 0.8 and 0.6 g· cm -3 for KOH (aq), Λ0 is nearly temperature-independent but increases linearly with decreasing density. The molal ion association constants ( KA(m)) for both KCl (aq) and KOH (aq) increase with increasing temperature and decreasing solution density. At corresponding temperatures and densities, ion association of KCl (aq) is similar in extent to NaCl (aq), whereas for KOH (aq) the values are slightly lower than for NaOH (aq). The log KA(m) values for KCl (aq) and KOH( aq) were calculated using the Shedlovsky equation exclusively from data obtained at temperatures ≥400°C and can be represented as functions of temperature ( T, Kelvin) and the logarithm of water density ( ϱw, g · cm -3) as follows: log K A(m)(KCI) = 0.753 100.21/T - (10.316 - 3598.9/T) log φ w and log K A(m)(KOH) = 10183 - 132.61/T - (13.002 - 621.8/T) logφ w These expressions apply strictly at ϱw ≥ 0.4 g · cm -3 where the measurements are most precise.

  12. Selective adsorption of Pt ions from chloride solutions obtained by leaching chlorinated spent automotive catalysts on ion exchange resin Diaion WA21J.

    PubMed

    Shen, Shaobo; Guishen, Liang; Pan, Tonglin; He, JunZhang; Guo, Zhanchen

    2011-12-15

    Thermodynamic and kinetics studies for adsorption of Pt ions complexes from the chloride solutions obtained by leaching chlorinated spent automotive catalysts on anionic exchange resin Diaion WA21J were carried out. It was found that only Si, Pt, Rh and Pd from the solution were selectively adsorbed on the resin Diaion WA21J more strongly. The adsorption equilibrium time for Pt ions was about 20 h. The isothermal adsorption of Pt ions was found to fit Langmuir, Freundlich and DKR models. The maximum monolayer adsorption capacities Q(max) and X(m) of Pt ions on the resin based on Langmuir and DKR model were 4.85, 5.36 and 5.69 mg/g as well as 5.01, 5.63 and 5.98 mg/g for temperatures 18°C, 28°C and 40°C, respectively. The apparent adsorption energy E(ad) based on DKR model were -11.79, -11.04 and -11.04 kJ/mol for the temperatures 18°C, 28°C and 40°C, respectively. Ion exchange was the mechanism involved in the adsorption process. The adsorption of Pt ions on the resin underwent pseudo-first-order kinetic process, and the apparent adsorption activation energy E(a,1) was 12.6 kJ/mol. The intraparticle diffusion of Pt ions was a main rate-controlling step in most of time of adsorption process.

  13. ZnO Solubility and Zn 2 Complexation by Chloride and Sulfate in Acidic Solutions to 290°C with In-Situ pH Measurement

    NASA Astrophysics Data System (ADS)

    Wesolowski, David J.; Bénézeth, Pascale; Palmer, Donald A.

    1998-03-01

    The solubility of zincite in mildly to strongly acidic aqueous solutions, according to the reaction ZnO + 2H + ⇔ Zn 2+ + H 2O, has been measured at ionic strengths of 0.03-1.0 (stoichiometric molal basis) from 50 to 290°C at saturation vapor pressure in sodium trifluoromethanesulfonate solutions (NaTriflate, a noncomplexing 1:1 electrolyte). The hydrogen-electrode concentration cells employed in this study permit continuous and highly accurate pH measurement at elevated temperatures, and periodic sampling to determine the dissolved metal content of the experimental solution. The solubility of zincite is shown to be reversible at 200°C by addition of acidic and basic titrants, at constant ionic strength. The equilibrium constant is precisely described (±0.05 log units) by the function log K = -4.0168 + 4527.66/T. One additional adjustable parameter, together with an extended Debye-Hückel function, is sufficient to model the ionic strength dependence of the reaction. The solubility product at infinite dilution obtained from this study is in quantitative agreement with the thermodynamic model of Ziemniak 1992. This experimental approach is demonstrated to be advantageous in studying the complexation of Zn 2+ with Cl - and SO 42-, by titrations involving the appropriate anion into NaTriflate solutions pre-equilibrated with zincite at constant temperature and ionic strength. Formation constants in 0.1 molal NaTriflate for the reaction Zn 2+ + yL z- ⇔ Zn(L) y2-yz are reported for ZnCl +, ZnCl 2° and ZnSO 4° at 200°C (log Q = 1.7 ± 0.1, 3.0 ± 0.1, and 2.6 ± 0.1, respectively). Estimates of the equilibrium constants for the chloride species at infinite dilution and 200°C are log K = 2.5 ± 0.1 (ZnCl +), and 4.2 ± 0.1 (ZnCl 2°). This value for the dichlorozinc complex agrees quantitatively with values reported by Bourcier and Barnes 1987 and Ruaya and Seward 1986. However, the latter authors give a value for the monochlorozinc complex (log K = 4.01 ± 0

  14. Influence of the anions on the N-cationic benzethonium salts in the solid state and solution: Chloride, bromide, hydroxide and citrate hydrates

    NASA Astrophysics Data System (ADS)

    Paradies, Henrich H.; Reichelt, Hendrik

    2016-06-01

    The crystal structures of the hydrated cationic surfactant benzethonium (Bzth) chloride, bromide, hydroxide, and citrate have been determined by X-ray diffraction analysis and compared with their structures in solution well above their critical micelle concentration. The differences in the nature of the various anions of the four Bzth-X materials lead to unique anion environments and 3-D molecular arrangements. The water molecule in the monoclinic Bzth-Cl or Bzth-Br forms is hydrogen bonded to the halides and particularly to the hydrogens of the methoxy groups of the Bzth moiety notwithstanding the weak Brønsted acidity of the methoxy hydrogens. The citrate strongly interacts with the hydrogens of the methoxy group forming an embedded anionic spherical cluster of a radius of 2.6 Å. The Bzth-OH crystallizes in a hexagonal lattice with two water molecules and reveals free water molecules forming hydrogen bonded channels through the Bzth-OH crystal along the c-axis. The distances between the cationic nitrogen and the halides are 4.04 Å and 4.20 Å, significantly longer than expected for typical van der Waals distances of 3.30 Å. The structures show weakly interacting, alternating apolar and polar layers, which run parallel to the crystallographic a-b planes or a-c planes. The Bzth-X salts were also examined in aqueous solution containing 20% (v/v) ethanol and 1.0 % (v/v) glycerol well above their critical micelle concentration by small-angle X-ray scattering (SAXS) and wide-angle X-ray scattering (WAXS). The [1,1,1] planes for the Bzth Cl or Br, the [0,0,2] and [1,1,0] planes for the Bzth-citrate, the [2,-1,0] planes and the [0,0,1] planes for the Bzth-OH found in the crystalline phase were also present in the solution phase, accordingly, the preservation of these phases are a strong indication of periodicity in the solution phase.

  15. Conformation evolution of oil contaminants onto aluminum oxide surface in aqueous solution: The effect of surface coverage

    NASA Astrophysics Data System (ADS)

    Xie, Wenkun; Liu, Haitao; Sun, Yazhou; Fu, Hongya; Liang, Yingchun

    2017-01-01

    The microscopic conformational change process of oil contaminants adhered onto perfect α-Al2O3 (0001) surface in aqueous solution was investigated by using all-atom classic molecular dynamics simulations. The change in removal mechanism of oil contaminants induced by surface coverage (surface area per molecule) was emphatically explored. Our simulation results strongly reveal that the increase in oil surface coverage induces an evident difference in microscopic detachment processes of oil contaminants. At a low surface coverage, oil contaminants can be thoroughly detached from solid surface. The whole detachment process could be divided into multi stages, including conformational change of oil contaminants on solid surface, dynamic motion of those in bulk solution and rapid migration of those from bulk solution to air/water interface. With surface coverage increasing, water diffusion becomes the key to induce conformational change and promote the detachment of oil contaminants. When oil surface coverage exceeds a threshold value, oil contaminants also undertake an evident conformational change process exhibiting typical characteristics but an incomplete detachment process occurs. All findings of the present study are helpful for the interpretation of the removal mechanism of oil contaminants on solid surface.

  16. Al/sub 2/S/sub 3/ preparation and use in electrolysis process for aluminum production

    DOEpatents

    Hsu, C.C.; Loutfy, R.O.; Yao, N.P.

    A continuous process for producing aluminum sulfide and for electrolyzing the aluminum sulfide to form metallic aluminum in which the aluminum sulfide is produced from aluminum oxide and COS or CS/sub 2/ in the presence of a chloride melt which also serves as the electrolysis bath. Circulation between the reactor and electrolysis cell is carried out to maintain the desired concentration of aluminum sulfide in the bath.

  17. Electrochemical generation of aluminum sorbent for fluoride adsorption.

    PubMed

    Yang, Chen-Yu; Dluhy, Robert

    2002-10-14

    Aluminum sorbent (Al-sorbent) was produced in a parallel-plate electrochemical reactor by anodic dissolution of aluminum electrodes in a dilute sodium chloride (NaCl) aqueous solution. The NaCl in the solution effectively reduced the power consumption and promoted the sorbent generation by depasivating the aluminum-water electrochemical system. The freshly generated Al-sorbent was able to reduce fluoride concentration from 16 to 2 mg/l in 2 min. The final concentration was further reduced to 0.1 mg/l by partial neutralization of the mixture to pH 6.3. The sorbent generation and fluoride adsorption was integrated into a single electrochemical reactor. The system was able to reduce the fluoride concentration from 16 to 6 mg/l in 2 min of treatment and to about 2 mg/l in 4 min. The effluent from the electrochemical system needs pH adjustment to bring the fluoride concentration down to less than 1 mg/l.

  18. Corrosion behavior of aluminum-lithium alloys

    SciTech Connect

    Garrard, W.N. )

    1994-03-01

    Corrosion behavior of three aluminum-lithium (Al-Li) alloys was investigated in aerated 0.5 M sodium sulfate (Na[sub 2]SO[sub 4]), deaerated 3.5% sodium chloride (NaCl), and aerated 3.5% NaCl. Corrosion behavior of the Aluminum Association (AA) alloys 2090-T8E41 (UNS A92090, sheet), AA 8090-T851 (UNS A98090, sheet), and AA 8090-T82551 (UNS A98090, bar) was compared to behavior of the conventional AA 7075-T6 (UNS A97075, sheet). Uniform corrosion was the predominant form of attack in aerated Na[sub 2]SO[sub 4] and deaerated NaCl, although some localized attack resulted from corrosion of intermetallics on specimen surfaces. Pitting was the main form of attack in aerated NaCl. In all three media, the sheet materials corroded at a similar rate, but the bar form of AA 8090 corroded at a lower rate. Pretreatment of the alloys by immersion in a cerium (Ce) solution inhibited pitting in aerated NaCl but only for a short period.

  19. pH-Dependent retention changes during membrane filtration of aluminum-coagulated solutions and the effect of precentrifugation.

    PubMed

    Bérubé, Denis; Dorea, Caetano

    2013-03-19

    During jar tests on alum-based drinking water treatment, dissolved Al determinations on solutions coagulated at pH ≥ 6.5 were not reproducible. These determinations were performed by inductively coupled plasma mass spectrometry after syringe filtration (0.45 μm polyethersulfone membrane). In order to better define these anomalies, the filtrates were collected in sequential fractions of 7.5 mL. At coagulation pHs of 6.5 and 7.0, retention changes were demonstrated by large filtrate concentration reductions at all temperatures tested (0.1, 5.0, and 17.0 °C). In all cases, the concentrations converged to levels <50 μg/L within the fourth sequential fraction. In comparison, no retention change was observed for jar tests conducted at the same temperatures but in the low range of the minimum solubility domain, at pHs 5.5 and 6.0. The retention changes were also eliminated by precentrifugation (7000 g for 45 min; pH 6.5-7.2). At weaker precentrifugation conditions, as well as by varying membrane surface area or membrane fouling, the filtrate concentrations behaved according to a barrier buildup at the membrane-solution interface by unsettled flocculation residuals. The influence of flocculation time and temperature emphasized the importance of reaction rates, which could be enhanced at the interface by concentration polarization effects. These phenomena have implications on analytical protocols and on filtration in full-scale treatment.

  20. Study of crevice-galvanic corrosion of aluminum

    NASA Technical Reports Server (NTRS)

    Draley, J. E.; Loess, R. E.; Mori, S.

    1967-01-01

    Corrosion effects of aluminum-copper and aluminum-nickel couples in oxygenated distilled water, and aluminum alloys in oxygenated copper sulfate solution were studied. One of each of the couples had a water tight seal, and showed no substantial corrosion, and of the unsealed couples, only the aluminum-copper developed corrosion.

  1. Iron-aluminum alloys having high room-temperature and method for making same

    DOEpatents

    Sikka, V.K.; McKamey, C.G.

    1993-08-24

    A wrought and annealed iron-aluminum alloy is described consisting essentially of 8 to 9.5% aluminum, an effective amount of chromium sufficient to promote resistance to aqueous corrosion of the alloy, and an alloying constituent selected from the group of elements consisting of an effective amount of molybdenum sufficient to promote solution hardening of the alloy and resistance of the alloy to pitting when exposed to solutions containing chloride, up to about 0.05% carbon with up to about 0.5% of a carbide former which combines with the carbon to form carbides for controlling grain growth at elevated temperatures, and mixtures thereof, and the balance iron, wherein said alloy has a single disordered [alpha] phase crystal structure, is substantially non-susceptible to hydrogen embrittlement, and has a room-temperature ductility of greater than 20%.

  2. Hydrogen chloride

    Integrated Risk Information System (IRIS)

    Hydrogen chloride ; CASRN 7647 - 01 - 0 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogeni

  3. Mepiquat chloride

    Integrated Risk Information System (IRIS)

    Mepiquat chloride ; CASRN 24307 - 26 - 4 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogen

  4. Acetyl chloride

    Integrated Risk Information System (IRIS)

    Acetyl chloride ; CASRN 75 - 36 - 5 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Ef

  5. Methyl chloride

    Integrated Risk Information System (IRIS)

    EPA / 635 / R01 / 003 TOXICOLOGICAL REVIEW OF METHYL CHLORIDE ( CAS No . 74 - 87 - 3 ) In Support of Summary Information on the Integrated Risk Information System ( IRIS ) June 2001 U.S . Environmental Protection Agency Washington , DC DISCLAIMER This document has been reviewed in accordance with U.

  6. Vinyl chloride

    Integrated Risk Information System (IRIS)

    EPA / 635R - 00 / 004 TOXICOLOGICAL REVIEW OF VINYL CHLORIDE ( CAS No . 75 - 01 - 4 ) In Support of Summary Information on the Integrated Risk Information System ( IRIS ) May 2000 U.S . Environmental Protection Agency Washington , DC DISCLAIMER This document has been reviewed in accordance with U.S

  7. Ethyl chloride

    Integrated Risk Information System (IRIS)

    Ethyl chloride ; CASRN 75 - 00 - 3 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Eff

  8. Benzyl chloride

    Integrated Risk Information System (IRIS)

    Benzyl chloride ; CASRN 100 - 44 - 7 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic E

  9. Allyl chloride

    Integrated Risk Information System (IRIS)

    Allyl chloride ; CASRN 107 - 05 - 1 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Ef

  10. Electrochemical evaluation of the effect of heat treatment and stress on the corrosion characteristics of 7050 aluminum in 3. 5% NaCl solution

    SciTech Connect

    Glass, R.S.; Estill, J.C.

    1985-11-01

    Potentiodynamic polarization curves have been used to evaluate (in a survey mode) the effect of heat treatment and stress on the corrosion behavior of 7050-XX aluminum in deaerated 3.5% NaCl solutions. Specimens, which were machined from extruded ring material, were examined in the as-received condition and following heat treatment at 580/sup 0/F for 0.5 min. The stress levels used in this study ranged from 40 to 90% of the 0.2% offset yield strength. Results indicate that within this stress range, using the given experimental method, medium, and timescales, that there is no significant trend for the effect of stress on the electrochemical-corrosion behavior for the materials examined. The heat-treated specimens have lower uniform corrosion rates than the as-received forms, but are more susceptible to pitting. However, pitting is not spontaneous for either material in this environment. In addition to investigating the variables of stress and heat treatment, we have also compared the behavior of specimens machined from three different orientations within extruded ring material. Generally, the longitudinal and circumferentially oriented specimens were more similar electrochemically than specimens obtained from the radial orientation. The radial specimens generally showed lower uniform corrosion rates and appeared to be less susceptible to pitting.

  11. Concentrated sodium chloride brine solutions as an additional treatment for preventing the introduction of nonindigenous species in the ballast tanks of ships declaring no ballast on board.

    PubMed

    Santagata, Scott; Bacela, Karolina; Reid, David F; Mclean, Kevin A; Cohen, Jill S; Cordell, Jeffery R; Brown, Christopher W; Johengen, Thomas H; Ruiz, Gregory M

    2009-02-01

    Currently, seawater flushing is the only management strategy for reducing the number of viable organisms in residual sediments and water of ballast tanks of vessels declaring no ballast on board (NOBOB) that traffic ports of the eastern United States. Previously, we identified several species of freshwater and brackish-water peracarid crustaceans able to survive the osmotic shock that occurs during open-ocean ballast water exchange and, potentially, to disperse over long distances via ballasted ships and NOBOB vessels. We tested the efficacy of concentrated sodium chloride brine solutions as an additional treatment for eradicating the halotolerant taxa often present in the ballast tanks of NOBOB ships. The lowest brine treatments (30 ppt for 1 h) caused 100% mortality in several species of cladocerans and copepods collected from oligohaline habitats. Several brackish-water peracarid crustaceans, however, including some that can survive in freshwater as well, required higher brine concentrations and longer exposure durations (45-60 ppt for 3-24 h). The most resilient animals were widely introduced peracarid crustaceans that generally prefer mesohaline habitats but do not tolerate freshwater (required brine treatments of 60-110 ppt for 3-24 h). Brine treatments (30 ppt) also required less time to cause 100% mortality for eight taxa compared with treatments using 34 ppt seawater. Based on these experiments and published data, we present treatment strategies for the ballast tank biota often associated with NOBOB vessels entering the Great Lakes region. We estimate the lethal dosage of brine for 95% of the species in our experiments to be 110 ppt (95% confidence interval, 85-192 ppt) when the exposure time is 1 h and 60 ppt (95% confidence interval, 48-98 ppt) when the exposure duration is 6 h or longer.

  12. Metal chloride cathode for a battery

    NASA Technical Reports Server (NTRS)

    Bugga, Ratnakumar V. (Inventor); Distefano, Salvador (Inventor); Bankston, C. Perry (Inventor)

    1991-01-01

    A method of fabricating a rechargeable battery is disclosed which includes a positive electrode which contains a chloride of a selected metal when the electrode is in its active state. The improvement comprises fabricating the positive electrode by: providing a porous matrix composed of a metal; providing a solution of the chloride of the selected metal; and impregnating the matrix with the chloride from the solution.

  13. Aluminum Analysis.

    ERIC Educational Resources Information Center

    Sumrall, William J.

    1998-01-01

    Presents three problems based on the price of aluminum designed to encourage students to be cooperative and to use an investigative approach to learning. Students collect and synthesize information, analyze results, and draw conclusions. (AIM)

  14. Galvanic corrosion of aluminum-matrix composites. Technical report No. 2, 1 Mar-31 Dec 90

    SciTech Connect

    Hihara, L.H.; Latanision, R.M.

    1991-02-01

    Galvanic-corrosion rates of Al-matrix composites were high in aerated chloride-containing solutions. Oxygen reduction was found to be the primary cathodic reaction. Aluminum corroded by pitting. The type of noble constituent (i.e., graphite, SiC, or TiB{sub 2}) also affected galvanic-corrosion rates. For example, results indicated that the galvanic-corrosion rate of Al should be about 30 times greater when coupled to graphite than when coupled to SiC or TiB{sub 2}. In dearated solutions, galvanic corrosion was negligible even if chlorides were present. The galvanic-corrosion rates were determined using the zero-resistance ammeter technique and from potentiodynamic polarization diagrams of ultrapure Al, 6061-T6 Al, graphite fiber, SiC, TiB2, and a commercial graphite fiber/6061-T6 Al metal-matrix composite.

  15. Adsorption of Supranol Yellow 4 GL from aqueous solution by surfactant-treated aluminum/chromium-intercalated bentonite.

    PubMed

    Bouberka, Z; Khenifi, A; Ait Mahamed, H; Haddou, B; Belkaid, N; Bettahar, N; Derriche, Z

    2009-02-15

    The aim of this paper is to study the adsorption of the acid dye Supranol Yellow 4 GL (S.Y. 4 GL) from aqueous solution on an inorgano-organo clay. Bentonite is naturally occurring clay with good exchanging ability. By exchanging its interlamellar cations with cetyltrimethylammonium bromide (CTAB) and hydroxyaluminic or chromium polycations, the properties of natural bentonite can be greatly improved. Batch adsorption tests of Supranol Yellow 4 GL were carried out at 20 degrees C and constant pH 6.5. To investigate the adsorption mechanisms, the simplified kinetic models, such as pseudo-first-order, pseudo-second-order, Elovich equation and intraparticle diffusion are tested. The results show that adsorption follows second-order rate kinetic. The correlation coefficients obtained for second-order kinetics model are greater than 0.998 indicating a better fitting of this equation. The experimental data are analysed by Langmuir, Freundlich and Elovich isotherms. The equilibrium adsorption capacity of anionic dye is determined from the Langmuir equation and found to be 142, 85 and 128, 20mg/g (standard deviation; Deltaq (%)=3.52 and 18.51) for CTAB-Cr-B and CTAB-Al-B, respectively.

  16. Recovery of aluminum from composite propellants

    NASA Technical Reports Server (NTRS)

    Shaw, G. C. (Inventor)

    1980-01-01

    Aluminum was recovered from solid rocket propellant containing a small amount of oxidizer by depolymerizing and dissolving propellant binders (containing functional or hydrolyzable groups in a solution of sodium methoxide) in an alcohol solvent optionally containing an aliphatic or aromatic hydrocarbon co-solvent. The solution was filtered to recover substantially all the aluminum in active form.

  17. An alternate to chromate conversion coatings for the corrosion protection of aluminum 2024-T3

    NASA Astrophysics Data System (ADS)

    Guo, Ruiguang

    Corrosion of high-strength aluminum alloys used for airspace application is an expensive and serious problem. The most significant environmental factor contributing to the corrosion of these alloys is water condensed from humid air and contaminated with soluble chloride salts. The Al 2024 series used for aircraft are particularly susceptible to corrosion in aqueous chloride solutions due to alloying constituents such as copper and other impurities. Chromates are efficient inhibitors of corrosion of aluminum in near neutral aqueous environments containing aggressive anions such as chlorides. Usually, aluminum alloys are initially protected by chromate conversion coatings. Additional polymer coatings are sometimes added during exposure to corrosive atmospheres such as marine environments. Although chromate coatings are widely used, they require the use of noxious solutions, so they have always presented effluent disposal problems. There are health and safety concerns over the use of chromates due to their toxicity and carcinogenic nature and, as a consequence, the environmental and health risks associated with the use of such coatings will be restricted in the future. It was these health and safety concerns that led to the development of alternative non-toxic coating processes with comparable adhesion properties and corrosion protection. A variety of process technologies are under development and are vying for acceptance in industrial markets. As an alternate conversion coating, a new titanate conversion coating was systematically researched and developed. Research concentrated on producing passive surfaces from a simple titanate solution using an immersion process. The corrosion resistance of the treated surface has been evaluated using simple, rapid electrochemical techniques as well as a more long-term salt spray test. Passivation by titanate conversion treatment exhibits many similarities to chromate conversion treatment. Based on this study of corrosion

  18. Stress Corrosion Cracking Behavior of Multipass TIG-Welded AA2219 Aluminum Alloy in 3.5 wt pct NaCl Solution

    NASA Astrophysics Data System (ADS)

    Venugopal, A.; Sreekumar, K.; Raja, V. S.

    2012-09-01

    The stress corrosion cracking (SCC) behavior of the AA2219 aluminum alloy in the single-pass (SP) and multipass (MP) welded conditions was examined and compared with that of the base metal (BM) in 3.5 wt pct NaCl solution using a slow-strain-rate technique (SSRT). The reduction in ductility was used as a parameter to evaluate the SCC susceptibility of both the BM and welded joints. The results showed that the ductility ratio ( ɛ NaCl/( ɛ air) was 0.97 and 0.96, respectively, for the BM and MP welded joint, and the same was marginally reduced to 0.9 for the SP welded joint. The fractographic examination of the failed samples revealed a typical ductile cracking morphology for all the base and welded joints, indicating the good environmental cracking resistance of this alloy under all welded conditions. To understand the decrease in the ductility of the SP welded joint, preexposure SSRT followed by microstructural observations were made, which showed that the decrease in ductility ratio of the SP welded joint was caused by the electrochemical pitting that assisted the nucleation of cracks in the form of corrosion induced mechanical cracking rather than true SCC failure of the alloy. The microstructural examination and polarization tests demonstrated a clear grain boundary (GB) sensitization of the PMZ, resulting in severe galvanic corrosion of the SP weld joint, which initiated the necessary conditions for the localized corrosion and cracking along the PMZ. The absence of PMZ and a refined fusion zone (FZ) structure because of the lesser heat input and postweld heating effect improved the galvanic corrosion resistance of the MP welded joint greatly, and thus, failure occurred along the FZ.

  19. Effectiveness of ophthalmic solution preservatives: a comparison of latanoprost with 0.02% benzalkonium chloride and travoprost with the sofZia preservative system

    PubMed Central

    2011-01-01

    Background Although in vitro and in vivo laboratory studies have suggested that benzalkonium chloride (BAK) in topical ophthalmic solutions may be detrimental to corneal epithelial cells, multiple short- and long-term clinical studies have provided evidence supporting the safety of BAK. Despite the conflicting evidence, BAK is the most commonly used preservative in ophthalmic products largely due to its proven antimicrobial efficacy. This study was designed to characterize the antimicrobial performance of two commonly used topical ocular hypotensive agents that employ different preservative systems: latanoprost 0.005% with 0.02% BAK and travoprost 0.004% with sofZia, a proprietary ionic buffer system. Methods Each product was tested for antimicrobial effectiveness by European Pharmacopoeia A (EP-A) standards, the most stringent standards of the three major compendia, which specify two early sampling time points (6 and 24 hours) not required by the United States Pharmacopeia or Japanese Pharmacopoeia. Aliquots were inoculated with between 105 and 106 colony-forming units of the test organisms: Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, Candida albicans and Aspergillus brasiliensis. Sampling and enumeration were conducted at protocol-defined time points through 28 days. Results BAK-containing latanoprost met EP-A criteria by immediately reducing all bacterial challenge organisms to the test sensitivity and fungal challenges within the first six hours while the preservative activity of travoprost with sofZia did not. Complete bacterial reduction by travoprost with sofZia was not shown until seven days into the test, and fungal reduction never exceeded the requisite 2 logs during the 28-day test. Travoprost with sofZia also did not meet EP-B criteria due to its limited effectiveness against Staphylococcus aureus. Both products satisfied United States and Japanese pharmacopoeial criteria. Conclusions Latanoprost with 0.02% BAK exhibited more

  20. Polymer gel electrolytes for application in aluminum deposition and rechargeable aluminum ion batteries

    SciTech Connect

    Sun, Xiao -Guang; Fang, Youxing; Jiang, Xueguang; Yoshii, Kazuki; Tsuda, Tetsuya; Dai, Sheng

    2015-10-22

    Polymer gel electrolyte using AlCl3 complexed acrylamide as functional monomer and ionic liquids based on acidic mixture of 1-ethyl-3-methylimidazolium chloride (EMImCl) and AlCl3 as plasticizer has been successfully prepared for the first time by free radical polymerization. Aluminum deposition is successfully obtained with a polymer gel membrane contianing 80 wt% ionic liquid. As a result, the polymer gel membranes are also good candidates for rechargeable aluminum ion batteries.

  1. Polymer gel electrolytes for application in aluminum deposition and rechargeable aluminum ion batteries

    DOE PAGES

    Sun, Xiao -Guang; Fang, Youxing; Jiang, Xueguang; ...

    2015-10-22

    Polymer gel electrolyte using AlCl3 complexed acrylamide as functional monomer and ionic liquids based on acidic mixture of 1-ethyl-3-methylimidazolium chloride (EMImCl) and AlCl3 as plasticizer has been successfully prepared for the first time by free radical polymerization. Aluminum deposition is successfully obtained with a polymer gel membrane contianing 80 wt% ionic liquid. As a result, the polymer gel membranes are also good candidates for rechargeable aluminum ion batteries.

  2. Aluminum industry applications for OTEC

    SciTech Connect

    Jones, M.S.; Leshaw, D.; Sathyanarayana, K.; Sprouse, A.M.; Thiagarajan, V.

    1980-12-01

    The objective of the program is to study the integration issues which must be resolved to realize the market potential of ocean thermal energy conversion (OTEC) power for the aluminum industry. The study established, as a baseline, an OTEC plant with an electrical output of 100 MWe which would power an aluminum reduction plant. The reduction plant would have a nominal annual output of about 60,000 metric tons of aluminum metal. Three modes of operation were studied, viz: 1. A reduction plant on shore and a floating OTEC power plant moored offshore supplying energy by cable. 2. A reduction plant on shore and a floating OTEC power plant at sea supplying energy by means of an ''energy bridge.'' 3. A floating reduction plant on the same platform as the OTEC power plant. For the floating OTEC/aluminum plantship, three reduction processes were examined. 1. The conventional Hall process with prebaked anodes. 2. The drained cathode Hall cell process. 3. The aluminum chloride reduction process.

  3. Aluminum alloy

    NASA Technical Reports Server (NTRS)

    Blackburn, Linda B. (Inventor); Starke, Edgar A., Jr. (Inventor)

    1989-01-01

    This invention relates to aluminum alloys, particularly to aluminum-copper-lithium alloys containing at least about 0.1 percent by weight of indium as an essential component, which are suitable for applications in aircraft and aerospace vehicles. At least about 0.1 percent by weight of indium is added as an essential component to an alloy which precipitates a T1 phase (Al2CuLi). This addition enhances the nucleation of the precipitate T1 phase, producing a microstructure which provides excellent strength as indicated by Rockwell hardness values and confirmed by standard tensile tests.

  4. Effect of dosing sequence and solution pH on floc properties of the compound bioflocculant-aluminum sulfate dual-coagulant in kaolin-humic acid solution treatment.

    PubMed

    Bo, Xiaowen; Gao, Baoyu; Peng, Nana; Wang, Yan; Yue, Qinyan; Zhao, Yingcan

    2012-06-01

    The compound bioflocculant (CBF)-aluminum sulfate (AS) dual-coagulant and AS were comparatively studied for the coagulation of kaolin-humic acid solution. Floc properties including floc growth rate, size, strength, recoverability and fractal dimension under different pH conditions were investigated by Mastersizer 2000. Results indicated that, the flocs formed by AS-CBF (AS dosed first) showed the largest size and the best recoverability across the pH range investigated. While flocs formed by CBF-AS gave the most compact structure. The three coagulants exhibited similar floc growth rate and strength. Moreover, flocs formed in acidic conditions were stronger and more recoverable but showed lower growth rate, smaller size and looser structure compared to those formed at pH>6 regardless of the coagulant used. Charge neutralization was the dominant mechanism for AS at low pH, while the coagulation mechanism transformed to enmeshment as the pH increased. There was an additional adsorption bridging effect for AS-CBF and CBF-AS.

  5. Production of sodium-22 from proton irradiated aluminum

    DOEpatents

    Taylor, Wayne A.; Heaton, Richard C.; Jamriska, David J.

    1996-01-01

    A process for selective separation of sodium-22 from a proton irradiated minum target including dissolving a proton irradiated aluminum target in hydrochloric acid to form a first solution including aluminum ions and sodium ions, separating a portion of the aluminum ions from the first solution by crystallization of an aluminum salt, contacting the remaining first solution with an anion exchange resin whereby ions selected from the group consisting of iron and copper are selectively absorbed by the anion exchange resin while aluminum ions and sodium ions remain in solution, contacting the solution with an cation exchange resin whereby aluminum ions and sodium ions are adsorbed by the cation exchange resin, and, contacting the cation exchange resin with an acid solution capable of selectively separating the adsorbed sodium ions from the cation exchange resin while aluminum ions remain adsorbed on the cation exchange resin is disclosed.

  6. Alloy solution hardening with solute pairs

    DOEpatents

    Mitchell, John W.

    1976-08-24

    Solution hardened alloys are formed by using at least two solutes which form associated solute pairs in the solvent metal lattice. Copper containing equal atomic percentages of aluminum and palladium is an example.

  7. Aluminum phosphide

    Integrated Risk Information System (IRIS)

    Aluminum phosphide ; CASRN 20859 - 73 - 8 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinoge

  8. 21 CFR 184.1426 - Magnesium chloride.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Magnesium chloride. 184.1426 Section 184.1426 Food... GRAS § 184.1426 Magnesium chloride. (a) Magnesium chloride (MgC12·6H2O, CAS Reg. No. 7786-30-3) is a... prepared by dissolving magnesium oxide, hydroxide, or carbonate in aqueous hydrochloric acid solution...

  9. Solution structure of oxidized rat microsomal cytochrome b5 in the presence of 2 M guanidinium chloride: monitoring the early steps in protein unfolding.

    PubMed

    Arnesano, F; Banci, L; Bertini, I; Koulougliotis, D

    1998-12-01

    One- and two-dimensional proton NMR spectroscopy has been employed in order to study the denaturation effect of guanidinium chloride (GdmCl) on the oxidized state of the A-form of rat microsomal cytochrome b5 (cyt b5). The protein rapidly starts losing the heme at denaturant concentrations larger than approximately 2.0 M and a largely unfolded protein is eventually obtained. An estimate of the unfolding kinetics is obtained and, by use of a two-state model (folded left and right arrow unfolded), a value for DeltaG degrees. Below this concentration, small (solution structure of the protein in the presence of 2 M GdmCl. By use of 1199 meaningful NOESY constraints (obtained from the assignment of 75% of the total protons) and 166 pseudocontact shifts, a family of 40 structures has been obtained through the program PSEUDYANA. The family was further refined through restrained energy minimization and the final root mean square deviation (RMSD) values with respect to the average structure are 0.67 +/- 0.10 A and 1.14 +/- 0.11 A for the backbone and heavy atoms, respectively. The quality of the present structure is equivalent to that of the one obtained recently for the native form [Arnesano et al. (1998) Biochemistry 37, 173-184], thus allowing a meaningful comparison between the two structures. Upon addition of 2 M GdmCl, significant local structural differences are induced to the protein backbone segments comprising residues 33-38 (helix alpha2) and 62-64 (end of helix alpha4-beginning of helix alpha5) while the overall folding scheme of the protein is still maintained. These protein regions form part of the "pocket

  10. Dehydration of highly concentrated solutions of fructose to 5-hydroxymethylfurfural in a cheap and sustainable choline chloride/carbon dioxide system.

    PubMed

    Liu, Fei; Barrault, Joël; De Oliveira Vigier, Karine; Jérôme, François

    2012-07-01

    Fête DES sciences: The dehydration of fructose and inulin to HMF is conveniently performed in a cheap and sustainable choline chloride/CO(2) deep eutectic solvent (DES) system. The medium is capable of converting high contents of fructose (>100 wt %) without affecting the yield of HMF (up to 72 %). The purity of the recovered HMF is >98%, and the reaction medium can be recycled.

  11. Interfacial preferential dissolution on silicon carbide particulate/aluminum composites

    SciTech Connect

    Yao, H.Y.; Zhu, R.Z.

    1998-07-01

    Previous studies on corrosion of discontinuously reinforced aluminum alloy composites have assumed that the role of the reinforcement-matrix interface is merely as a preferable site for pitting. In this work, the interfacial preferential dissolution (IPD) occurring on silicon carbide particulate/aluminum (SiC{sub p}/Al) composites in a medium of aqueous sodium chloride (NaCl) solution was studied. IPD was quite distinct from pitting. IPD occurred on the composites with either a pure aluminum matrix or an aluminum alloy Al 2024 (UNS A92024) matrix, whether they were fabricated by a cast process or by a powder metallurgy process. In the light of elastoplastic mechanics, the width of the plastically deformed zone around SiC particles (created by the contraction misfit between SiC particles and the matrix during quenching) was deduced to be 0.5 D, where D is the diameter of the SiC particles. This was in agreement with the measured width of the IPD region (0.3 D to 0.4 D). It was concluded that IPD was caused by the poor integrity of the surface oxide film upon the plastically deformed zone near the interface and was independent of the chemical, metallurgical, and galvanic coupling factors around the interface, if any. A copper-deposition experiment indicated this poor integrity. IPD caused increased dissolution at SiC clusters and uniform corrosion for the composites with high SiC content. Moreover, IPD and pitting suppressed each other by a means of cathodic protection.

  12. Differences in antibacterial activity of benzalkonium chloride.

    PubMed

    Richards, R M; Mizrahi, L M

    1978-03-01

    Benzalkonium solutions obtained from different manufacturers were shown to have different activities. This difference in activity was related to the composition of the benzalkonium chloride. The potential seriousness of this situation is emphasized, and a recommendation is made that the official monographs on benzalkonium chloride be amended appropriately, noting the apparently superior antibacterial activity of the tetradecyl (C14) homolog.

  13. Aluminum induced proteome changes in tomato cotyledons

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Cotyledons of tomato seedlings that germinated in a 20 µM AlK(SO4)2 solution remained chlorotic while those germinated in an aluminum free medium were normal (green) in color. Previously, we have reported the effect of aluminum toxicity on root proteome in tomato seedlings (Zhou et al. J Exp Bot, 20...

  14. Studies of removal of platinum(IV) ion microquantities from the model solutions of aluminium, copper, iron, nickel and zinc chloride macroquantities on the anion exchanger Duolite S 37.

    PubMed

    Hubicki, Z; Wójcik, G

    2006-08-25

    Platinum has been widely applied in catalytic industry and the recovery of noble metals from industrial wastes becomes an economic issue. The laboratory studies of platinum(IV) microquantities removal from 1M aluminium, copper, iron, nickel and zinc chloride solutions in 0.1M hydrochloric acid solutions on the anion exchanger Duolite S 37 of the functional secondary and tertiary amine groups were carried out. For this anion exchanger the fraction extracted values (%E, Pt(IV)) as well as the sorption isotherms were determined depending on the kind of aqueous phase and phase contact time. Moreover, the bed and weight distribution coefficients as well as working and total ion-exchange capacities were calculated from the platinum(IV) breakthrough curves. Kinetic parameters were determined.

  15. Effect of sodium chloride on glassy and crystalline transitions of wheat starch treated with high hydrostatic pressure: Prediction of solute-induced barostability from nonmonotonic solute-induced thermostability

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Wheat starch was high hydrostatic pressure (HHP)-treated in various sodium chloride (NaCl) concentrations (0 to near-saturation), in order to explore the effects of salt on glassy and crystalline transitions of starch during the treatment, using differential scanning calorimetry (DSC). For wheat st...

  16. Paradoxical bronchospasm from benzalkonium chloride (BAC) preservative in albuterol nebulizer solution in a patient with acute severe asthma. A case report and literature review of airway effects of BAC.

    PubMed

    George, Mathew; Joshi, Saumya Vinod; Concepcion, Emily; Lee, Haesoon

    2017-01-01

    Nebulized bronchodilator solutions are available in the United States as both nonsterile and sterile-filled products. Sulfites, benzalkonium chloride (BAC), or chlorobutanol are added to nonsterile products to prevent bacterial growth. Bronchoconstriction from inhaled BAC is cumulative, prolonged, and correlates directly with basal airway responsiveness. The multi-dose dropper bottle of albuterol sulfate solution contains 50 μg BAC per/2.5 mg of albuterol, which may be below or at the lower limit of the threshold dose for bronchoconstriction. However, with repeated albuterol nebulization, the effect can be additive and cumulative, often exceeding the bronchoconstriction threshold. We report a case of a 17 years old patient, who received 32 mg of BAC via nebulization over a period of 3.5 days that probably caused persistent bronchospasm evidenced by failure to improve clinically and to increase peak expiratory flow rate (PEFR) from 125 L/min (27% of predicted value) to 300 L/min (68% of predicted value) within 2 hours of withdrawing BAC. The patient's respiratory status and PEFR improved dramatically once the nebulization solution was switched to BAC free lev-albuterol solution. The pediatric providers, particularly the emergency department physicians, intensivists and pulmonologists need to be aware of this rare albeit possible toxicity to the respiratory system caused by BAC used as a preservative in albuterol nebulizer solution.

  17. Making Positive Electrodes For Sodium/Metal Chloride Cells

    NASA Technical Reports Server (NTRS)

    Bugga, Ratnakumar V.; Distefano, Salvador; Bankston, C. Perry

    1992-01-01

    High coulombic yields provided by sodium/metal chloride battery in which cathode formed by impregnating sintered nickel plaque with saturated solution of nickel chloride. Charge/discharge cycling of nickel chloride electrode results in very little loss of capacity. Used in spacecraft, electric land vehicles, and other applications in which high-energy-density power systems required.

  18. Advances in the electrodeposition of aluminum from ionic liquid based electrolytes

    NASA Astrophysics Data System (ADS)

    Leadbetter, Kirt C.

    Aluminum plating is of considerable technical and economic interest because it provides an eco-friendly substitute for cadmium coatings used on many military systems. However, cadmium has been determined to be a significant environmental safety and occupational health (ESOH) hazard because of its toxicity and carcinogenic nature. Furthermore, the cost of treating and disposing of generated wastes, which often contain cyanide, is costly and is becoming prohibitive in the face of increasingly stringent regulatory standards. The non-toxic alternative aluminum is equivalent or superior in performance to cadmium. In addition, it could serve to provide an alternative to hexavalent chromium coatings used on military systems for similar reasons to that of cadmium. Aluminum is a beneficial alternative in that it demonstrates self-healing corrosion resistance in the form of a tightly-bound, impervious oxide layer. A successfully plated layer would be serviceable over a wider temperature range, 925 °F for aluminum compared to 450 oF for cadmium. In addition, an aluminum layer can be anodized to make it non-conducting and colorable. In consideration of the plating process, aluminum cannot be deposited from aqueous solutions because of its reduction potential. Therefore, nonaqueous electrolytes are required for deposition. Currently, aluminum can be electrodeposited in nonaqueous processes that use hazardous chemicals such as toluene and pyrophoric aluminum alkyls. Electrodeposition from ionic liquids provides the potential for a safer method that could be easily scaled up for industrial application. The plating process could be performed at a lower temperature and higher current density than other commercially available aluminum electrodeposition processes; thus a reduced process cost could be possible. The current ionic liquid based electrolytes are more expensive; however production on a larger scale and a long electrolyte lifetime are associated with a reduction in price

  19. Comparison of the crevice corrosion resistance of Alloys 625 and 22 in concentrated chloride solution from 60 to 95 degrees C

    SciTech Connect

    Kehler, B A; Illevbare, G O; Scully, J R

    1999-12-06

    The effects of electrolyte composition and oxide film age on the crevice corrosion properties of alloys 625 and 22 were studied at temperatures ranging from 60 to 95 C in concentrated chloride electrolytes. Critical potentials were determined using conventional current density thresholds and comparisons were made between 625 and 22 on the basis of these critical potentials. Air aged 22 specimens exhibited the highest resistance to crevice corrosion at 95 C in terms of critical crevice potentials, while freshly polished 22 exhibited the lowest resistance. Studies over the entire, temperature range showed that air aged 22 is more resistant to crevice corrosion than air aged 625 as evidenced by higher critical crevice potentials. As the temperature was lowered from 95 to 8O C, critical crevice potentials for 22 either approached or exceeded experimentally determined Cr (Mo, Ni) transpassive potentials.

  20. Aluminum-carbon composite electrode

    DOEpatents

    Farahmandi, C. Joseph; Dispennette, John M.

    1998-07-07

    A high performance double layer capacitor having an electric double layer formed in the interface between activated carbon and an electrolyte is disclosed. The high performance double layer capacitor includes a pair of aluminum impregnated carbon composite electrodes having an evenly distributed and continuous path of aluminum impregnated within an activated carbon fiber preform saturated with a high performance electrolytic solution. The high performance double layer capacitor is capable of delivering at least 5 Wh/kg of useful energy at power ratings of at least 600 W/kg.