Measurement of the ratio of C3+ and O4+ ions produced by ECRIS to prepare a laser cooling experiment at storage rings

International Nuclear Information System (INIS)

Zhu, X.L.; Wen, W.Q.; Ma, X.; Li, J.Y.; Feng, W.T.; Zhang, R.T.; Wang, Enliang; Yan, S.; Guo, D.L.; Hai, B.; Qian, D.B.; Zhang, P.; Xu, S.; Zhao, D.M.; Yang, J.; Zhang, D.C.; Li, B.; Gao, Y.; Huang, Z.K.; Wang, H.B.

2014-01-01

To prepare the upcoming laser cooling of relativistic C 3+ ion beams at the experimental Cooler Storage Ring (CSRe), a novel experiment was performed using a reaction microscope to determine the ratio of C 3+ ions in mixed ion beams of C 3+ and O 4+ that are produced by an Electron Cyclotron Resonance Ion Source (ECRIS). The mixed ion beams at an energy of 4 keV/u were directed to collide on a supersonic helium gas target. Using the single-electron capture channel and the coincidence technique, the fractions of C 3+ and O 4+ ions in the primary beam were obtained. Using different injection gases for ECRIS, including O 2 , CO, CO 2 , and CH 4 , at a fixed radio-frequency power of 300 W, the measured results showed that the fraction of C 3+ ions was greater than 70% for the injection gases of CO and CO 2 . These measured results are very important and helpful for the upcoming laser cooling experiments

A method for the estimation of the enthalpy of formation of mixed oxides in Al2O3-Ln2O3 systems

International Nuclear Information System (INIS)

Vonka, P.; Leitner, J.

2009-01-01

A new method is proposed for the estimation of the enthalpy of formation (Δ ox H) of various Al 2 O 3 -Ln 2 O 3 mixed oxides from the constituent binary oxides. Our method is based on Pauling's concept of electronegativity and, in particular, on the relation between the enthalpy of formation of a binary oxide and the difference between the electronegativities of the oxide-forming element and oxygen. This relation is extended to mixed oxides with a simple formula given for the calculation of Δ ox H. The parameters of this equation were fitted using published experimental values of Δ ox H derived from high-temperature oxide melt solution calorimetry. Using our proposed method, we obtained a standard deviation (σ) of 4.87 kJ mol -1 for this data set. Taking into account regularities within the lanthanide series, we then estimated the Δ ox H values for Al 2 O 3 -Ln 2 O 3 mixed oxides. The values estimated using our method were compared with those obtained by Aronson's and Zhuang's empirical methods, both of which give significantly poorer results. - Graphical abstract: Enthalpy of formation of Ln-Al-O oxides from the constituent binary ones.

Correlating oxygen vacancies and phase ratio/interface with efficient photocatalytic activity in mixed phase TiO2

International Nuclear Information System (INIS)

Verma, Ranjana; Samdarshi, S.K.

2015-01-01

Graphical abstract: The correlation of interfacial behavior and oxygen vacancies in mixed phase titania nanoparticles on their performance as photocatalyst has been investigated to explain the impact of photoactivity under UV and visible irradiation compared to pristine counterparts. The defects at the junction effectively reduce the band gap as well decrease the carrier recombination to enhance the photocatalytic activity. - Highlights: • Pristine and mixed phases (A/R ratio) TiO 2 synthesized by sol gel route. • Photoactivity variation has been correlated with the changes in the phase ratio. • Enhanced UV and visible activity attributable to oxygen vacancy present at the interface. • Role of A/R ratio and oxygen vacancy in the photoactivity of mixed TiO 2 depicted through a model. - Abstract: The photocatalytic activity is a result of the synergy of a succession of phenomena-photogeneration, separation, and participation of the charge carriers in redox reaction at the catalyst surface. While the extent of photogeneration is assessable in terms of absorption spectrum (band gap), the redox reaction can be correlated to specific surface area. However the respective change in the photocatalytic activity has not been rationally and consistently correlated with the above mentioned parameters. A satisfactory explanation of suppression of recombination based on separation of carriers due to differential mobility/diffusivity in the material phase(s) and/or intrinsic potential barrier exists but its correlation with common identifiable parameter/characteristics is still elusive. This paper attempts to address this issue by correlating the carrier separation with the phase ratio (phase interface) in mixed phase titania and generalizing it with the presence of oxygen vacancy at the phase interface. It essentially appears to complete the quest for identifiable parameters in the sequence of phenomena, which endow a photocatalyst with an efficient activity level. It has

Steam reforming of ethanol over Co3O4–Fe2O3 mixed oxides

KAUST Repository

Abdelkader, A.

2013-05-03

Co3O4, Fe2O3 and a mixture of the two oxides Co-Fe (molar ratio of Co3O4/Fe 2O3 = 0.67 and atomic ratio of Co/Fe = 1) were prepared by the calcination of cobalt oxalate and/or iron oxalate salts at 500 C for 2 h in static air using water as a solvent/dispersing agent. The catalysts were studied in the steam reforming of ethanol to investigate the effect of the partial substitution of Co3O4 with Fe2O 3 on the catalytic behaviour. The reforming activity over Fe 2O3, while initially high, underwent fast deactivation. In comparison, over the Co-Fe catalyst both the H2 yield and stability were higher than that found over the pure Co3O4 or Fe 2O3 catalysts. DRIFTS-MS studies under the reaction feed highlighted that the Co-Fe catalyst had increased amounts of adsorbed OH/water; similar to Fe2O3. Increasing the amount of reactive species (water/OH species) adsorbed on the Co-Fe catalyst surface is proposed to facilitate the steam reforming reaction rather than decomposition reactions reducing by-product formation and providing a higher H2 yield. © Copyright © 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

Enhanced Conductivity at the Interface of Li2O ratio B2O3 Nanocomposites: Atomistic Models

International Nuclear Information System (INIS)

Islam, Mazharul M.; Bredow, Thomas; Indris, Sylvio; Heitjans, Paul

2007-01-01

A theoretical investigation at density-functional level of Li ion conduction at the interfaces in Li 2 O ratio B 2 O 3 nanocomposites is presented. The structural disorder at the Li 2 O(111) ratio B 2 O 3 (001) interface leads to reduced defect formation energies for Li vacancies and Frenkel defects compared to Li 2 O surfaces. The average activation energy for Li + diffusion in the interface region is in the range of the values for Li 2 O. It is therefore concluded that the enhanced Li conductivity of Li 2 O ratio B 2 O 3 nanocomposites is mainly due to the increased defect concentration

Analysis Influence of Mixing Gd2O3 in the Silicide Fuel Element to Core Excess Reactivity of RSG-GAS

International Nuclear Information System (INIS)

Susilo, Jati

2004-01-01

Gadolinium (Gd 2 O 3 ) is a burnable poison material mixed in the pin fuel element of the LWR core used to decrease core excess reactivity. In this research, analysis influence of mixing Gd 2 O 3 in the silicide fuel element to excess reactivity of the RSG-GAS core had been done. Equivalent cell of the equilibrium core developed by L.E.Strawbridge from Westing House Co. burn-up calculation has been done using SRAC-PIJ computer code achieve infinite multiplication factor (k x ). Value of Gd 2 O 3 concentration in the fuel element (pcm) showed by mass ratio of Gd 2 O 3 (gram) to that U 3 Si 2 (gram) times 10 5 , that is 0 pcm ∼ 100 pcm. From the calculation results analysis showed that Gd 2 O 3 concentration added should be considered. because a large number of Gd 2 O 3 will result in not achieving criticality at the Beginning Of Cycle. The maximum concentration of Gd 2 O 3 for RSG-GAS equilibrium fueled silicide 2.96 grU/cc is 80 pcm or 52.02 mgram/fuel plate. Maximum reduction of core excess reactivity due to mixing of Gd 2 O 3 in the RSG-GAS silicide fuels was around 1.502 %Δk/k, and hence not achieving the standard nominal excess reactivity for RSG-GAS core using high density of U 3 Si 2 -Al fuel. (author)

Improvement in ferroelectric properties of Pt/PZT/Pt capacitors etched as a function of Ar/O2 gas mixing ratio into Cl2/CF4 plasma

International Nuclear Information System (INIS)

Lim, Kyu-Tae; Koo, Seong-Mo; Kim, Kyoung-Tae; Kim, Dong-Pyo; Kim, Chang-Il

2004-01-01

In this work, to investigate improvement of the damage using oxygen containing plasma, we etched PZT films as a function of Ar (x%)/O 2 (y%) gas mixing ratio in Cl 2 (56%)/CF 4 (14%) plasma (where the sum of x and y is 30). The maximum etch rate of the PZT thin films was 146 nm/min for Ar (30%)/O 2 (0%) added into the Cl 2 /CF 4 plasma. After the etching, the plasma-induced damages were characterized in terms of hysteresis curves, leakage current, switching polarization and retention capacity as a function of the gas mixing ratio. When the ferroelectric properties of PZT films were etched as a function of O 2 and Ar and the gas mixing ratios were compared, the value of remnant polarization in O 2 (30%) added Cl 2 /CF 4 plasma is higher than that in Ar (30%). The results showed that after the etching the charges accumulated by oxygen vacancies prevented further domain switching at the top electrode-ferroelectric interface and created leakage current because of modification of the interfacial Schottky barrier during the etching process. The physical damage to the near surface and the crystal structure of the etched PZT thin films was evaluated by using X-ray diffraction (XRD). The remnant polarization, leakage current, retention and fatigue properties are improved with increasing O 2 content. From XRD results, the improvement in the ferroelectric properties of PZT capacitors etched in O 2 containing plasma was consistent with the increased intensities of the (100) and (200) peaks

A simple dissolved metals mixing method to produce high-purity MgTiO3 nanocrystals

International Nuclear Information System (INIS)

Pratapa, Suminar; Baqiya, Malik A.; Istianah,; Lestari, Rina; Angela, Riyan

2014-01-01

A simple dissolved metals mixing method has been effectively used to produce high-purity MgTiO 3 (MT) nanocrystals. The method involves the mixing of independently dissolved magnesium and titanium metal powders in hydrochloric acid followed by calcination. The phase purity and nanocrystallinity were determined by making use of laboratory x-ray diffraction data, to which Rietveld-based analyses were performed. Results showed that the method yielded only one type magnesium titanate powders, i.e. MgTiO 3 , with no Mg 2 TiO 4 or MgTi 2 O 5 phases. The presence of residual rutile or periclase was controlled by adding excessive Mg up to 5% (mol) in the stoichiometric mixing. The method also resulted in MT nanocrystals with estimated average crystallite size of 76±2 nm after calcination at 600°C and 150±4 nm (at 800°C). A transmission electron micrograph confirmed the formation of the nanocrystallites

DISSOLUTION BEHAVIOR OF BIOACTIVE GLASS CERAMICS WITH DIFFERENT CaO/MgO RATIOS

Directory of Open Access Journals (Sweden)

MUHAMMAD USMAN HASHMI

2010-03-01

Full Text Available In this work, powders of three different compositions, each having 34 SiO2-14.5 P2O5-1 CaF2-0.5 MgF (% wt and ratio of CaO/MgO varying from 11.5:1 to 1:11.5 were thoroughly mixed and melted under oxy-acetylene flame in a fire clay crucible that made the glass formation cheaper in time and cost. The melt of each composition was quenched in water to form three different glasses. Every glass was sintered at 950°C to form three glass ceramics named G1, G2 and G3 respectively. To study the dissolution behavior, each sample was immersed in a simulated body fluid (SBF for 2, 5, 10, 20 and 25 days at room temperature. Thin film XRD analysis revealed that the samples with larger CaO/MgO ratio exhibited better bioactivity. pH of SBF increased efficiently in case of G1 whereas in case of G2 and G3, this increase was slower due to greater amount of MgO. The concentrations of Ca, P, Mg and Si ions were measured by Atomic Absorption Spectroscopy. EDS analysis showed the increase in P and Ca ions and presence of C in G1 after 5 days immersion and after 10 days, in case of G2 indicating the higher formation rate of hydroxycarbonate Apatite layer in G1 as compared to G2 due to greater CaO/MgO ratio whereas in G3 Mg-hydroxycarbonate apatite (Ca(Mg5(CO3(PO43(OH (heneuite layer was recognized after 20 days showing the least bioactivity due to very large amount of Mg and the least CaO/MgO ratio.

Measurement of low-ppm mixing ratios of water vapor in the upper troposphere and lower stratosphere using chemical ionization mass spectrometry

Directory of Open Access Journals (Sweden)

T. D. Thornberry

2013-06-01

Full Text Available A chemical ionization mass spectrometer (CIMS instrument has been developed for the fast, precise, and accurate measurement of water vapor (H2O at low mixing ratios in the upper troposphere and lower stratosphere (UT/LS. A low-pressure flow of sample air passes through an ionization volume containing an α-particle radiation source, resulting in a cascade of ion-molecule reactions that produce hydronium ions (H3O+ from ambient H2O. The production of H3O+ ions from ambient H2O depends on pressure and flow through the ion source, which were tightly controlled in order to maintain the measurement sensitivity independent of changes in the airborne sampling environment. The instrument was calibrated every 45 min in flight by introducing a series of H2O mixing ratios between 0.5 and 153 parts per million (ppm, 10−6 mol mol−1 generated by Pt-catalyzed oxidation of H2 standards while overflowing the inlet with dry synthetic air. The CIMS H2O instrument was deployed in an unpressurized payload area aboard the NASA WB-57F high-altitude research aircraft during the Mid-latitude Airborne Cirrus Properties Experiment (MACPEX mission in March and April 2011. The instrument performed successfully during seven flights, measuring H2O mixing ratios below 5 ppm in the lower stratosphere at altitudes up to 17.7 km, and as low as 3.5 ppm near the tropopause. Data were acquired at 10 Hz and reported as 1 s averages. In-flight calibrations demonstrated a typical sensitivity of 2000 Hz ppm−1 at 3 ppm with a signal to noise ratio (2 σ, 1 s greater than 32. The total measurement uncertainty was 9 to 11%, derived from the uncertainty in the in situ calibrations.

A single gas chromatograph for accurate atmospheric mixing ratio measurements of CO2, CH4, N2O, SF6 and CO

NARCIS (Netherlands)

van der Laan, S.; Neubert, R. E. M.; Meijer, H. A. J.; Simpson, W.R.

2009-01-01

We present an adapted gas chromatograph capable of measuring simultaneously and semi-continuously the atmospheric mixing ratios of the greenhouse gases CO2, CH4, N2O and SF6 and the trace gas CO with high precision and long-term stability. The novelty of our design is that all species are measured

Effect of the Molar Ratio of B2O3 to Bi2O3 in Al Paste with Bi2O3-B2O3-ZnO Glass on Screen Printed Contact Formation and Si Solar Cell Performance

Science.gov (United States)

Kim, Bit-Na; Kim, Hyeong Jun; Chang, Hyo Sik; Hong, Hyun Seon; Ryu, Sung-Soo; Lee, Heon

2013-10-01

In this study, eco-friendly Pb-free Bi2O3-B2O3-ZnO glass frits were chosen as an inorganic additive for the Al paste used in Si solar cells. The effects of the molar ratio of Bi2O3 to B2O3 in the glass composition on the electrical resistance of the Al electrode and on the cell performance were investigated. The results showed that as the molar ratio of Bi2O3 to B2O3 increased, the glass transition temperature and softening temperature decreased because of the reduced glass viscosity. In Al screen-printed Si solar cells, as the molar ratio of Bi2O3 to B2O3 increased, the sheet electrical resistance of the Al electrode decreased and the cell efficiency increased. The uniformity and thickness of the back-surface field was significantly influenced by the glass composition.

Synergy effects in mixed Bi2O3, MoO3 and V2O5 catalysts for selective oxidation of propylene

DEFF Research Database (Denmark)

Nguyen, Tien The; Le, Thang Minh; Truong, Duc Duc

2012-01-01

% Bi2Mo3O12 and 78.57 mol% BiVO4), corresponding to the compound Bi1-x/3V1-xMoxO4 with x = 0.45 (Bi0.85V0.55Mo0.45O4), exhibited the highest activity for the selective oxidation of propylene to acrolein. The mixed sample prepared chemically by a sol–gel method possessed higher activity than...

Performance of diesel engine using diesel B3 mixed with crude palm oil.

Science.gov (United States)

Namliwan, Nattapong; Wongwuttanasatian, Tanakorn

2014-01-01

The objective of this study was to test the performance of diesel engine using diesel B3 mixed with crude palm oil in ratios of 95 : 5, 90 : 10, and 85 : 15, respectively, and to compare the results with diesel B3. According to the tests, they showed that the physical properties of the mixed fuel in the ratio of 95 : 5 were closest to those of diesel B3. The performance of the diesel engine that used mixed fuels had 5-17% lower torque and power than that of diesel B3. The specific fuel consumption of mixed fuels was 7-33% higher than using diesel B3. The components of gas emissions by using mixed fuel had 1.6-52% fewer amount of carbon monoxide (CO), carbon dioxide (CO2), sulfur dioxide (SO2), and oxygen (O2) than those of diesel B3. On the other hand, nitric oxide (NO) and nitrogen oxides (NO X ) emissions when using mixed fuels were 10-39% higher than diesel B3. By comparing the physical properties, the performance of the engine, and the amount of gas emissions of mixed fuel, we found out that the 95 : 5 ratio by volume was a suitable ratio for agricultural diesel engine (low-speed diesel engine).

FORMATION CONDITIONS OF ICY MATERIALS IN COMET C/2004 Q2 (MACHHOLZ). I. MIXING RATIOS OF ORGANIC VOLATILES

International Nuclear Information System (INIS)

Kobayashi, Hitomi; Kawakita, Hideyo

2009-01-01

We observed comet C/2004 Q2 (Machholz) with the Keck II telescope in late 2005 January and we obtained the spectra of C/2004 Q2 including many emission lines of volatile species such as H 2 O, HCN, C 2 H 2 , NH 3 , CH 4 , C 2 H 6 , CH 3 OH, and H 2 CO with high-signal-to-noise ratios. Based on our observations, we determined the mixing ratios of the molecules relative to H 2 O in C/2004 Q2. Since C/2004 Q2 is one of Oort Cloud comets, it is interesting to compare our results with other Oort Cloud comets. The mixing ratios of C 2 H 2 /H 2 O and C 2 H 6 /H 2 O in C/2004 Q2 are lower than typical Oort Cloud comets. Especially, C 2 H 2 /H 2 O ratio in C/2004 Q2 is as lower as Jupiter Family comets. However, mixing ratios of other molecules in C/2004 Q2 are similar to typical Oort Cloud comets. C/2004 Q2 might be the intermediate type between Oort Cloud and Jupiter Family comets. To investigate the formation conditions of such intermediate type comet, we focused on the (C 2 H 2 +C 2 H 6 )/H 2 O ratios and C 2 H 6 /(C 2 H 6 +C 2 H 2 ) ratios in comets from the viewpoint of conversion from C 2 H 2 to C 2 H 6 in the precometary ices. We found that (C 2 H 2 +C 2 H 6 )/H 2 O ratio in C/2004 Q2 is lower than the ratio in typical Oort Cloud comets while C 2 H 6 /(C 2 H 6 +C 2 H 2 ) ratio in C/2004 Q2 is consistent with the ratio of the typical Oort Cloud comets and Jupiter family comets. If we assume that the cometary volatiles such as H 2 O, CH 4 , and C 2 H 2 formed similar environment, the C 2 H 6 /(C 2 H 6 +C 2 H 2 ) ratio might not be sensitive in the temperature range where hydrogen-addition reactions occurred and cometesimals formed (∼30 K). We employed the dynamical-evolutional model and the chemical-evolutional model to determine the formation region of C/2004 Q2 more precisely. We found that comet C/2004 Q2 might have formed in relatively inner region of the solar nebula than the typical Oort Cloud comet (but slightly further than 5 AU from the proto-Sun).

Actinide Oxidation State and O/M Ratio in Hypostoichiometric Uranium-Plutonium-Americium U0.750Pu0.246Am0.004O2-x Mixed Oxides.

Science.gov (United States)

Vauchy, Romain; Belin, Renaud C; Robisson, Anne-Charlotte; Lebreton, Florent; Aufore, Laurence; Scheinost, Andreas C; Martin, Philippe M

2016-03-07

Innovative americium-bearing uranium-plutonium mixed oxides U1-yPuyO2-x are envisioned as nuclear fuel for sodium-cooled fast neutron reactors (SFRs). The oxygen-to-metal (O/M) ratio, directly related to the oxidation state of cations, affects many of the fuel properties. Thus, a thorough knowledge of its variation with the sintering conditions is essential. The aim of this work is to follow the oxidation state of uranium, plutonium, and americium, and so the O/M ratio, in U0.750Pu0.246Am0.004O2-x samples sintered for 4 h at 2023 K in various Ar + 5% H2 + z vpm H2O (z = ∼ 15, ∼ 90, and ∼ 200) gas mixtures. The O/M ratios were determined by gravimetry, XAS, and XRD and evidenced a partial oxidation of the samples at room temperature. Finally, by comparing XANES and EXAFS results to that of a previous study, we demonstrate that the presence of uranium does not influence the interactions between americium and plutonium and that the differences in the O/M ratio between the investigated conditions is controlled by the reduction of plutonium. We also discuss the role of the homogeneity of cation distribution, as determined by EPMA, on the mechanisms involved in the reduction process.

Performance of Diesel Engine Using Diesel B3 Mixed with Crude Palm Oil

Science.gov (United States)

Namliwan, Nattapong; Wongwuttanasatian, Tanakorn

2014-01-01

The objective of this study was to test the performance of diesel engine using diesel B3 mixed with crude palm oil in ratios of 95 : 5, 90 : 10, and 85 : 15, respectively, and to compare the results with diesel B3. According to the tests, they showed that the physical properties of the mixed fuel in the ratio of 95 : 5 were closest to those of diesel B3. The performance of the diesel engine that used mixed fuels had 5–17% lower torque and power than that of diesel B3. The specific fuel consumption of mixed fuels was 7–33% higher than using diesel B3. The components of gas emissions by using mixed fuel had 1.6–52% fewer amount of carbon monoxide (CO), carbon dioxide (CO2), sulfur dioxide (SO2), and oxygen (O2) than those of diesel B3. On the other hand, nitric oxide (NO) and nitrogen oxides (NOX) emissions when using mixed fuels were 10–39% higher than diesel B3. By comparing the physical properties, the performance of the engine, and the amount of gas emissions of mixed fuel, we found out that the 95 : 5 ratio by volume was a suitable ratio for agricultural diesel engine (low-speed diesel engine). PMID:24688402

Spectral characterization of mechanically synthesized MoO3-CuO nanocomposite

Science.gov (United States)

Sundeep, Dola; Gopala Krishna, A.; Ravikumar, R. V. S. S. N.; Vijaya Kumar, T.; Daniel Ephraim, S.; Pavan, Y. L.

2016-01-01

In this work, MoO3-CuO metal oxide composite nanopowders are prepared by simple mechanochemical assisted synthesis technique with the stoichiometric weight ratios of MoO3 and CuO as 2.3:1 and 3.3:1, respectively. The structural and spectroscopic properties of the as-synthesised samples are characterised by XRD, SEM with EDS, FT-IR, Raman spectroscopy and TGA/DTA. X-ray diffraction pattern demonstrates the peaks correspond to orthorhombic phase of α-MoO3 and monoclinic phase of β-CuO. The average crystalline sizes of the 2.3:1 and 3.3:1 samples were found to be 16 and 24 nm, respectively, which are supported by Williamson-Hall (W-H) calculations. The correlations between the milling rotational speeds with morphological characteristics are revealed by the SEM images. The fundamental modes of Mo=O and Cu-O were analysed by FT-IR. Raman analysis has provided the qualitative information about the structure of the mixed oxide composite. Thermogravimetry analysis and Differential Thermal Analysis (DTA) of MoO3-CuO have revealed that the dual phase mixed oxide composite is stable up to 709 °C with a negligible weight loss. Based on the above, it can be inferred that the synthesised mixed lubricous oxide nanocomposite could be used as a solid lubricant at elevated temperatures.

β-Ga2O3 versus ε-Ga2O3: Control of the crystal phase composition of gallium oxide thin film prepared by metal-organic chemical vapor deposition

Science.gov (United States)

Zhuo, Yi; Chen, Zimin; Tu, Wenbin; Ma, Xuejin; Pei, Yanli; Wang, Gang

2017-10-01

Gallium oxide thin films of β and ε phase were grown on c-plane sapphire using metal-organic chemical vapor deposition and the phase compositions were analyzed using X-ray diffraction. The epitaxial phase diagram was constructed as a function of the growth temperature and VI/III ratio. A low growth temperature and low VI/III ratio were beneficial for the formation of hexagonal-type ε-Ga2O3. Further structure analysis revealed that the epitaxial relationship between ε-Ga2O3 and c-plane sapphire is ε-Ga2O3 (0001) || Al2O3 (0001) and ε-Ga2O3 || Al2O3 . The structural evolution of the mixed-phase sample during film thickening was investigated. By reducing the growth rate, the film evolved from a mixed phase to the energetically favored ε phase. Based on these results, a Ga2O3 thin film with a phase-pure ε-Ga2O3 upper layer was successfully obtained.

Influence of Zn/Fe Molar Ratio on Optical and Magnetic Properties of ZnO and ZnFe2O4 Nanocrystal as Calcined Products of Layered Double Hydroxides

Directory of Open Access Journals (Sweden)

Abdullah Ahmed Ali Ahmed

2014-01-01

Full Text Available The coprecipitation method has been used to synthesize layered double hydroxide (Zn-Fe-LDH nanostructure at different Zn2+/Fe3+ molar ratios. The structural properties of samples were studied using powder X-ray diffraction (PXRD. LDH samples were calcined at 600°C to produce mixed oxides (ZnO and ZnFe2O4. The crystallite size of mixed oxide was found in the nanometer scale (18.1 nm for ZnFe2O4 and 43.3 nm for ZnO. The photocatalytic activity of the calcination products was investigated using ultraviolet-visible-near infrared (UV-VIS-NIR diffuse reflectance spectroscopy. The magnetic properties of calcined LDHs were investigated using a vibrating sample magnetometer (VSM. The calcined samples showed a paramagnetic behavior for all Zn2+/Fe3+ molar ratios. The effect of molar ratio on magnetic susceptibility of the calcined samples was also studied.

Determination of the oxygen-metal-ratio of uranium-americium mixed oxides

International Nuclear Information System (INIS)

Bartscher, W.

1982-01-01

During the dissolution of uranium-americium mixed oxides in phosphoric acid under nitrogen tetravalent uranium is oxidized by tetravalent americium. The obtained hexavalent uranium is determined by constant potential coulometry. The coulombs measured are equivalent to the oxygen in excess of the minimum composition of UO 2 x AmO 1 . 5 . The total uranium content of the sample is determined in a subsequent coulometric titration. The oxygen-metal ratio of the sample can be calculated for a given uranium-americium ratio. An excess of uranium dioxide is necessary in order to suppress the oxidation of water by tetravalent americium. The standard deviation of the method is 0.0017 O/M units. (orig.) [de

Mixing Ratios and Photostationary State of NO and NO2 Observed During the POPCORN Field Campaign at a Rural Site in Germany

NARCIS (Netherlands)

Rohrer, F.; Brüning, D.; Grobler, E.S.; Weber, M.; Ehhalt, D.H.; Neubert, R.; Schüßler, W.; Levin, I.

1998-01-01

Ambient mixing ratios of NO, NO2, and O3 were determined together with the photolysis frequency of NO2, JNO2, at a rural, agricultural site in Germany. The data were collected during the POPCORN-campaign from August 1 to August 24, 1994, in a maize field 6 m above ground. The medians of the NO, NO2,

Study on the Effect of Different Fe2O3/ZrO2 Ratio on the Properties of Silicate Glass Fibers

Directory of Open Access Journals (Sweden)

Jianxun Liu

2017-01-01

Full Text Available A series of silicate glass fibers with different ratios of Fe2O3/ZrO2 were prepared, and their corrosion resistance, mass loss, and strength loss were characterized. The crystallization and melting properties of the fibers were analyzed by differential scanning calorimetry (DSC, high temperature viscometer, and high temperature microscope. The results show that the deformation temperature, sphere temperature, hemisphere temperature, and crystallization temperature of the fiber initially decrease and then increase with the increase of Fe2O3/ZrO2 ratio, while the molding temperature decreases with the increase of the ratio of Fe2O3/ZrO2. When the ratio is close to 1 : 1, its alkali resistance is almost same as that of AR-glass fiber, and the drawing process performance is better. However, with the increase of the ratio, its alkali resistance continues to decline and the poor wire drawing performance is not conducive to the drawing operation.

3D coordination polymers with nitrilotriacetic and 4,4'-bipyridyl mixed ligands: structural variation based on dinuclear or tetranuclear subunits assisted by Na-O and/or O-H...O interactions.

Science.gov (United States)

Lü, Xing-Qiang; Jiang, Ji-Jun; Chen, Chun-Long; Kang, Bei-Sheng; Su, Cheng-Yong

2005-06-27

The reactions of Cu(II) with the mixed nitrilotriacetic acid (H3NTA) and 4,4'-bipyridyl (4,4'-bpy) ligands in different metal-to-ligand ratios in the presence of NaOH and NaClO4 afforded two complexes, Na3[Cu2(NTA)2(4,4'-bpy)]ClO4 x 5H2O (1) and [Cu2(NTA) (4,4'-bpy)2]ClO4 x 4H2O (2). The two complexes have been characterized by elemental analysis, IR, XRD, and single-crystal X-ray diffraction. 1 contains a basic doubly negatively charged [Cu2(NTA)2(4,4'-bpy)]2- dinuclear unit which was further assembled via multiple Na-O and O-H...O interactions into a three-dimensional (3D) pillared-layer structure. 2 features a two-dimensional (2D) undulated brick-wall architecture containing a basic doubly positively charged [Cu4(NTA)2(4,4'-bpy)2]2+ tetranuclear unit. The 2D network possesses large cavities hosting guest molecules and was further assembled via O-H...O hydrogen bonds into a 3D structure with several channels running in different directions.

Effect of Sr/Ti Ratio on the Photocatalytic Properties of SrTiO3

International Nuclear Information System (INIS)

Sulaeman, U; Yin, S; Sato, T

2011-01-01

Since strontium titanate is a wide gap semiconductor, it requires UV light to generate the photocatalytic activities. Modification of strontium titanate to show photocatalytic activity under visible light irradiation is the essential work to efficiently utilize the sun light energy for environmental application. It is expected that the synthesis of SrTiO 3 with variation of Sr/Ti atomic ratio could induce the defect crystals having unique photocatalytic properties. The SrTiO 3 with various Sr/Ti atomic ratios were synthesized by microwave-assisted solvothermal reaction of SrCl 2 .6H 2 O and Ti(OC 3 H 7 ) 4 in KOH aqueous solutions with different atomic ratios of Sr/Ti. The products were characterized by TG-DTA, XRD and DRS. The photocatalytic activity was determined by DeNO x ability using LED lamps with the wavelengths of 627 nm (red), 530 nm (green), 445 nm (blue) and 390 nm (UV). The nanoparticles of perovskite type SrTiO 3 with the particle size of 30-40 nm were successfully synthesized. The visible light responsive photocatalytic activity was generated by adding excess amount of Sr. The photocatalytic activity in visible light could be enhanced by an increase in the Sr/Ti atomic ratio up to 1.25, indicating that the visible light responsive photocatalytic activity is due to the generation of new band gap between the conduction band and valence band of SrTiO 3 by the formation of oxygen vacancy.

Synthesis of geopolymer from spent FCC: Effect of SiO2/Al2O<3 and Na2O/SiO2 molar ratios

Directory of Open Access Journals (Sweden)

Trochez, J. J.

2015-03-01

Full Text Available This paper assesses the feasibility of using a spent fluid catalytic cracking catalyst (SFCC as precursor for the production of geopolymers. The mechanical and structural characterization of alkali-activated SFCC binders formulated with different overall (activator + solid precursor SiO2/Al2O3 and Na2O/SiO2 molar ratios are reported. Formation of an aluminosilicate ‘geopolymer’ gel is observed under all conditions of activation used, along with formation of zeolites. Increased SiO2/Al2O3 induces the formation of geopolymers with reduced mechanical strength, for all the Na2O/SiO2 ratios assessed, which is associated with excess silicate species supplied by the activator. This is least significant at increased alkalinity conditions (higher Na2O/SiO2 ratios, as larger extents of reaction of the spent catalyst are achieved. SiO2/Al2O3 and Na2O/SiO2 ratios of 2.4 and 0.25, respectively, promote the highest compressive strength (67 MPa. This study elucidates the great potential of using SFCC as precursor to produce sustainable ceramic-like materials via alkali-activation.Este artículo estudia la factibilidad de usar un catalizador gastado del proceso de craqueo (SFCC para la producción de geopolímeros. Se evalúan las características mecánicas y estructurales de los geopolímeros producidos con diferentes relaciones molares (activador + precursor solido de SiO2/Al2O3 y Na2O/SiO2. La formación de un gel geopolimérico de tipo aluminosilicato se observa a las diferentes condiciones evaluadas, así como la formación de zeolitas. Un incremento en la relación SiO2/Al2O3 genera geopolímeros de baja resistencia mecánica, a las diferentes relaciones molares Na2O/SiO2 evaluadas, como consecuencia del exceso de especies silicato provenientes del activador. Este efecto es menos significativo al incrementar las condiciones de alcalinidad (mayores relaciones Na2O/SiO2, ya que un mayor grado de reacción del catalizador gastado es alcanzado. Las

Mixed Alkali Effect in (40-x)K2O-xLi2O-10Na2O-50B2O3 Glasses - Physical and Optical Absorption Studies

Science.gov (United States)

Samee, M. A.; Ahmmad, Shaikh Kareem; Taqiullah, Sair. Md.; Edukondalu, A.; Bale, Shashidhar; Rahman, Syed

So far only a handful of publications have been concerned with the study of the mixed alkali effect in borate glasses containing three types of alkali ions. In the present work, the mixed alkali effect (MAE) has been investigated in the glass system (40-x) K2O-x Li2O -10Na2O-50B2O3.(0≤x≤40 mol%) through density and modulated DSC studies. The density and glass transition temperature of the present glasses varies non-linearly exhibiting mixed alkali effect. We report the mixed alkali effect in the present glasses through optical properties. From the absorption edge studies, the various values of optical band gap (Eo) and Urbach energy (ΔE) have been evaluated. The values of Eo and ΔE show non-linear behavior with compositional parameter showing the mixed alkali effect. The band gap energy based average electronic polarizability of oxide ions αO2-(Eo), optical basicity A(Eo), and Yamashita-Kurosawa’s interaction parameter A(Eo) have been examined to check the correlations among them and bonding character. Based on good correlation among electronic polarizability of oxide ions, optical basicity and interaction parameter, the present K2O- Li2O-Na2O-B2O3 glasses are classified as normal ionic (basic) oxides.

Synthesis and characterization of mixed phases in the Ca–Co–O system using the Pechini method

Energy Technology Data Exchange (ETDEWEB)

Tran, Hoa; Mehta, Tejas [College of DuPage, 425 Fawell Blvd, Glen Ellyn, IL 60137-6599 (United States); Zeller, Matthias [Department of Chemistry, Youngstown State University, 1 University Plaza, Youngstown, OH 44555-3663 (United States); Jarman, Richard H., E-mail: Jarman@cod.edu [College of DuPage, 425 Fawell Blvd, Glen Ellyn, IL 60137-6599 (United States)

2013-07-15

Highlights: ► We have prepared mixed Ca–Co–O phases using the Pechini method. ► Reaction times are reduced relative to conventional solid-state synthesis. ► Products have high surface area suitable for ceramic processing. ► Product composition is dictated by both kinetic and thermodynamic control. ► A revised phase diagram of the Ca–Co–O system is proposed. - Abstract: The synthesis of mixed phases in the Ca–Co–O system using the Pechini method was investigated. The phases CaCo{sub 2}O{sub 4}, Ca{sub 3}Co{sub 4}O{sub 9} and Ca{sub 3}Co{sub 2}O{sub 6}, which can be expressed in terms of the molar ratios of the binary oxides (CaO:Co{sub 2}O{sub 3}) as (1:1), (3:2) and (3:1) respectively, were obtained in pure form. Powder X-ray diffraction data showed they are comparable with materials obtained by conventional solid-state synthesis. The mild synthesis conditions of the Pechini method allowed the evolution of the Ca–Co–O phases to be studied as a function of temperature and heating time. Both variables have a strong influence on the composition of the products, indicating that both kinetic and thermodynamic factors play a role, with the former being of more importance at lower temperatures. The (1:1) phase, previously not identified in the phase diagram of the Ca–Co–O system, was obtained preferentially across the composition range below ca. 650 °C. The (3:2) phase was preferred until ca. 800 °C. At even higher temperatures, the (3:1) phase is obtained. The upper thermal stability limit of mixed phases in the Ca–Co–O system increases with the Ca:Co ratio. An updated phase diagram for the Ca–Co–O system is proposed.

Accurate prediction of H3O+ and D3O+ sensitivity coefficients to probe a variable proton-to-electron mass ratio

Science.gov (United States)

Owens, A.; Yurchenko, S. N.; Polyansky, O. L.; Ovsyannikov, R. I.; Thiel, W.; Špirko, V.

2015-12-01

The mass sensitivity of the vibration-rotation-inversion transitions of H316O+, H318O+, and D316O+ is investigated variationally using the nuclear motion program TROVE (Yurchenko, Thiel & Jensen). The calculations utilize new high-level ab initio potential energy and dipole moment surfaces. Along with the mass dependence, frequency data and Einstein A coefficients are computed for all transitions probed. Particular attention is paid to the Δ|k| = 3 and Δ|k - l| = 3 transitions comprising the accidentally coinciding |J, K = 0, v2 = 0+> and |J, K = 3, v2 = 0-> rotation-inversion energy levels. The newly computed probes exhibit sensitivities comparable to their ammonia and methanol counterparts, thus demonstrating their potential for testing the cosmological stability of the proton-to-electron mass ratio. The theoretical TROVE results are in close agreement with sensitivities obtained using the non-rigid and rigid inverter approximate models, confirming that the ab initio theory used in the present study is adequate.

MARKETING MIX BY BED OCCUPANCY RATIO (BOR

Directory of Open Access Journals (Sweden)

Abdul Muhith

2017-04-01

Full Text Available Introduction: Bed Occupancy Ratio (BOR in RSI Arafah Mojosari during the last three years are at under ideal rate and the lowest of the three existing hospitals in the area of Mojosari. The purpose of this study was to determine the relationship marketing mix with Bed Occupancy Ratio in RSI Arafah Mojosari. Methods: This research uses analytic methods with crossectional approach. Variables in the study is marketing mix and Bed Occupancy Ratio (BOR. The population in this study were all patients hospitalized in the RSI Arafah Mojosari. Samples amounted 44 respondents taken by the Stratified random sampling technique. Data were collected using the questionnaire and analyzed using Fisher's Exact test. Result: The results obtained more than 50% of respondents (59.1% rate well against the marketing mix is developed by the hospital management and the majority of respondents (79.5% are in the treatment room that has a number BOR is not ideal. Fisher Exact test test results obtained probabililty value=0.02<0.05 so that H0 is rejected, which means there is a relationship marketing mix with the Bed Occupancy Ratio in RSI Arafah Mojosari. Discussion: Hospitals which able to develop the marketing mix very well, can attract consumers to use inpatient services at the hospital, with that BOR value will increase as the increased use of inpatient services. Hospital management must be able to formulate a good marketing mix strategy that hospital marketing objectives can be achieved. Conformity between service quality and service rates must be addressed, otherwise it extent of media promotions can attract patients to inpatient services.

Thermoluminescence induced by UV radiation in ZrO2-La2O3 and ZrO2-CeO2 mixed systems

International Nuclear Information System (INIS)

Estrada G, R.; Salas C, P.; Mendoza A, D.; Gonzalez, P.R.

2002-01-01

Nowadays, the development of catalytic materials by means of pure or mixed oxides mainly as TiO 2 , Al 2 O 3 , ZrO 2 , La 2 O 3 and CeO 2 used as support or active phases, are widely used in oxidation-reduction reactions in the chemical industry and in petroleum refining processes. the cerium and lanthanum oxides in zircon, have been studied recently in processes for reduction of pollutant gases (SO x , NO x , etc.). They result very interesting for resolving the problems of environmental pollution. Moreover, it has been observed that some of these materials are highly sensitive to ultraviolet radiation (UV), characteristic that can be took in advantage for detecting this type of radiation. In this work the preliminary obtained results on the thermoluminescent response (Tl) induced by the UV radiation in ZrO 2 -La 2 O 3 and ZrO 2 -CeO 2 mixed systems obtained by the sol-gel method are presented. The results show that the first system has a high sensitivity to UV radiation with a Tl curve composed by three peaks, two ones of greater intensity located in 70 and 140 Centigrade degrees. Likewise it was observed that for both materials, the peak located at low temperature is fadeout in few minutes after irradiation, while that the second one peak presented very good stability, resulting promising for dosimetric applications in UV radiation fields. (Author)

Conversion of Syngas-Derived C2+ Mixed Oxygenates to C3-C5 Olefins over ZnxZryOz Mixed Oxides Catalysts

Energy Technology Data Exchange (ETDEWEB)

Smith, Colin D.; Lebarbier, Vanessa M.; Flake, Matthew D.; Ramasamy, Karthikeyan K.; Kovarik, Libor; Bowden, Mark E.; Onfroy, Thomas; Dagle, Robert A.

2016-04-01

In this study we report on a ZnxZryOz mixed oxide type catalyst capable of converting a syngas-derived C2+ mixed oxygenate feedstock to isobutene-rich olefins. Aqueous model feed comprising of ethanol, acetaldehyde, acetic acid, ethyl acetate, methanol, and propanol was used as representative liquid product derived from a Rh-based mixed oxygenate synthesis catalyst. Greater than 50% carbon yield to C3-C5 mixed olefins was demonstrated when operating at 400-450oC and 1 atm. In order to rationalize formation of the products observed feed components were individually evaluated. Major constituents of the feed mixture (ethanol, acetaldehyde, acetic acid, and ethyl acetate) were found to produce isobutene-rich olefins. C-C coupling was also demonstrated for propanol feedstock - a minor constituent of the mixed oxygenate feed - producing branched C6 olefins, revealing scalability to alcohols higher than ethanol following an analogous reaction pathway. Using ethanol and propanol feed mixtures, cross-coupling reactions produced mixtures of C4, C5, and C6 branched olefins. The presence of H2 in the feed was found to facilitate hydrogenation of the ketone intermediates, thus producing straight chain olefins as byproducts. While activity loss from coking is observed complete catalyst regeneration is achieved by employing mild oxidation. For conversion of the mixed oxygenate feed a Zr/Zn ratio of 2.5 and a reaction temperature of 450oC provides the best balance of stability, activity, and selectivity. X-ray diffraction and scanning transmission electron microscopy analysis reveals the presence of primarily cubic phase ZrO2 and a minor amount of the monoclinic phase, with ZnO being highly dispersed in the lattice. The presence of ZnO appears to stabilize the cubic phase resulting in less monoclinic phase as the ZnO concentration increases. Infrared spectroscopy shows the mixed oxide acid sites are characterized as primarily Lewis type acidity. The direct relationship between

XPS analysis of UxCe1-xO2±δ and determination of oxygen to metal ratio

International Nuclear Information System (INIS)

Bera, Santanu; Mittal, V.K.; Venkata Krishnan, R.; Saravanan, T.; Velmurugan, S.; Nagarajan, K.; Narasimhan, S.V.

2009-01-01

The chemical states of U and Ce in the solid solutions of UO 2 and CeO 2 are studied using the X-ray photoelectron spectroscopy. A detailed analyses on U 4f and Ce 3d photoelectron peaks revealed the presence of Ce 3+ and U 5+ /U 6+ states in the mixed oxides. The oxygen to metal ratios in different compositions of mixed oxides were estimated from the quantity of different chemical states of U and Ce present in mixed oxides.

Study on adsorption of rhodamine B onto Beta zeolites by tuning SiO2/Al2O3 ratio.

Science.gov (United States)

Cheng, Zhi-Lin; Li, Yan-Xiang; Liu, Zan

2018-02-01

The exploration of the relationship between zeolite composition and adsorption performance favored to facilitate its better application in removal of the hazardous substances from water. The adsorption capacity of rhodamine B (RB) onto Beta zeolite from aqueous solution was reported. The relationship between SiO 2 /Al 2 O 3 ratio and adsorption capacity of Beta zeolite for RB was explored. The structure and physical properties of Beta zeolites with various SiO 2 /Al 2 O 3 ratios were determined by XRD, FTIR, TEM, BET, UV-vis and so on characterizations. The adsorption behavior of rhodamine B onto Beta zeolite matched to Langmuir adsorption isotherm and more suitable description for the adsorption kinetics was a pseudo-second-order reaction model. The maximum adsorption capacity of the as-prepared Beta zeolite with SiO 2 /Al 2 O 3 = 18.4 was up to 27.97mg/g. Copyright © 2017 Elsevier Inc. All rights reserved.

Diurnal variations in H2O2, O3, PAN, HNO3 and aldehyde concentrations and NO/NO2 ratios at Rishiri Island, Japan: Potential influence from iodine chemistry

International Nuclear Information System (INIS)

Kanaya, Yugo; Tanimoto, Hiroshi; Matsumoto, Jun; Furutani, Hiroshi; Hashimoto, Shigeru; Komazaki, Yuichi; Tanaka, Shigeru; Yokouchi, Yoko; Kato, Shungo; Kajii, Yoshizumi; Akimoto, Hajime

2007-01-01

The presence of iodine chemistry, hypothesized due to the overprediction of HO 2 levels by a photochemical box model at Rishiri Island in June 2000, was quantitatively tested against the observed NO/NO 2 ratios and the net production rates of ozone. The observed NO/NO 2 ratios were reproduced reasonably well by considering the conversion of NO to NO 2 by IO, whose amount was calculated so as to reproduce the observed HO 2 levels. However, the net production rates of ozone were calculated to be negative when such high mixing ratios of IO were considered, which was inconsistent with the observed buildup of ozone during daytime. These results suggest that iodine chemistry may not be the sole mechanism for the reduced mixing ratios of HO 2 , or that 'hot spots' for iodine chemistry were present. Diurnal variations in the mixing ratios of HCHO, CH 3 CHO, peroxy acetyl nitrate (PAN) and HNO 3 observed during the study are presented along with the simulated ones. The box model simulations suggest that the effect of iodine chemistry on these concentrations is small and that important sources of CH 3 CHO and sinks of PAN are probably missing from our current understanding of the tropospheric chemistry mechanism

Effects of the Ho{sup 3+}/Yb{sup 3+} concentration ratio on the structure and photoluminescence of ZnO films

Energy Technology Data Exchange (ETDEWEB)

Xu, Boxu [School of Materials Science and Engineering, Tianjin Polytechnic University, Tianjin 300387 (China); Wang, Pei [Auditing Department, Tianjin Polytechnic University, Tianjin 300387 (China); Meng, Xiaoqi; Zou, Kaishun [School of Materials Science and Engineering, Tianjin Polytechnic University, Tianjin 300387 (China); Liu, Juncheng, E-mail: jchliu@tjpu.edu.cn [School of Materials Science and Engineering, Tianjin Polytechnic University, Tianjin 300387 (China)

2016-07-15

To improve the efficiency of photoluminescent films, this study investigates the effects of the Ho{sup 3+}/Yb{sup 3+} concentration ratio on the structure and up-conversion photoluminescence of ZnO films prepared by the sol–gel method and the spin-coating technique. ZnO maintained its hexagonal wurtzite structure after doping with rare earth ions. The ZnO films consist of round granules, the average size of which increases as the Ho{sup 3+}/Yb{sup 3+} concentration ratio increases. Once the ratio exceeds 1:2, the film's granules significantly coarsen, and the surface roughness slightly increases. When the film is pumped with a 980-nm laser, two intense emission bands are observed in the up-conversion emission spectrum, with a green band centered at 550 nm and a red band centered at 660 nm, corresponding to the Ho{sup 3+}: {sup 5}S{sub 2}/{sup 5}F{sub 4}→{sup 5}I{sub 8}, and {sup 5}F{sub 5}→{sup 5}I{sub 8} transitions, respectively. In addition, as the Ho{sup 3+}/Yb{sup 3+} concentration ratio increases, the intensity of the film's upconversion luminescence first increases and then decreases, reaching a maximum at a concentration ratio of 1:2, with a peak of about four times the minimum value.

A Mixed-Valent Molybdenum Monophosphate with a Layer Structure: KMo 3P 2O 14

Science.gov (United States)

Guesdon, A.; Borel, M. M.; Leclaire, A.; Grandin, A.; Raveau, B.

1994-03-01

A new mixed-valent molybdenum monophosphate with a layer structure KMo 3P 2O 14 has been isolated. It crystallizes in the space group P2 1/ m with a = 8.599(2) Å, b = 6.392(2) Å, c = 10.602(1) Å, and β = 111.65(2)°. The layers [Mo 3P 2O 14] ∞ are parallel to (100) and consist of [MoPO 8] ∞ chains running along limitb→ , in which one MoO 6 octahedron alternates with one PO 4 tetrahedron. In fact, four [MoPO 8] ∞ chains share the corners of their polyhedra and the edges of their octahedra, forming [Mo 4P 4O 24] ∞ columns which are linked through MoO 5 bipyramids along limitc→. The K + ions interleaved between these layers are surrounded by eight oxygens, forming bicapped trigonal prisms KO 8. Besides the unusual trigonal bipyramids MoO 5, this structure is also characterized by a tendency to the localization of the electrons, since one octahedral site is occupied by Mo(V), whereas the other octahedral site and the trigonal bipyramid are occupied by Mo(VI). The similarity of this structure with pure octahedral layer structures suggests the possibility of generating various derivatives, and of ion exchange properties.

O/M ratio measurement in pure and mixed oxide fuels - where are we now?

Energy Technology Data Exchange (ETDEWEB)

Rubin, J.; Chidester, K.; Thompson, M. [Los Alamos National Lab., NM (United States)

2001-07-01

The scale-down in the US and Russian nuclear weapons stockpiles has produced a surplus of weapons grade plutonium and highly enriched uranium. The incorporation into mixed-oxide fuel (MOX) is one of the currently favored routes for surplus weapons-grade plutonium. The use of MOX as a nuclear reactor fuel is well established, particularly in Europe and Japan but not in the US. The primary purpose of this investigation was to evaluate existing analytical techniques for their applicability to O/M (oxygen-to-metal ratio) measurements of MOX derived from excess weapons plutonium. The second objective of this investigation was to bring up-to-date the literature on O/M measurement methods, which has not been undertaken in over 20 years. There are several classification schemes that can be used to organize O/M measurement methods. The most popular schemes are based on (a) whether the analysis is performed in solution (wet chemical) or on solid material (dry), and (b) whether the concentration of major constituents are analyzed directly (direct) or are inferred (indirect). Solid state coulometric titration is currently used extensively in studies of phase equilibria, defect chemistry, thermochemical measurement of oxides, including ferrites. Regardless of which indirect method is used (solid state coulometric titration or thermogravimetry), a primary, direct method will also be required for the establishment of the MO{sub 2} reference state, determination of method bias, and periodic calibration. It was recommended that the following direct method be adapted for this purpose: oxygen measurement by inert gas fusion/carbon reduction, and total U, Pu by controlled potential coulometry. In a table are listed the experimental values of accuracy for about 30 O/M methods. (A.C.)

Effect of molar ratios of MgO/Al{sub 2}O{sub 3} on the sintering behavior and thermal shock resistance of MgOAl{sub 2}O{sub 3}SiO{sub 2} composite ceramics

Energy Technology Data Exchange (ETDEWEB)

Feng, Dong, E-mail: 1078155409@qq.com [School of High Temperature Materials and Magnesium Resource Engineering, University of Science and Technology Liaoning, Anshan 114051 (China); Luo, Xudong, E-mail: luoxudongs@aliyun.com [School of High Temperature Materials and Magnesium Resource Engineering, University of Science and Technology Liaoning, Anshan 114051 (China); Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China); Zhang, Guodong [School of High Temperature Materials and Magnesium Resource Engineering, University of Science and Technology Liaoning, Anshan 114051 (China); Xie, Zhipeng [Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China)

2017-01-01

In order to determine the relationship between the property of MgOAl{sub 2}O{sub 3}SiO{sub 2} composite ceramics and molar ratios of MgO/Al{sub 2}O{sub 3}, especially the sintering behavior and thermal shock resistance, the MgOAl{sub 2}O{sub 3}SiO{sub 2} composite ceramics were fabricated with micro-size MgO, Al{sub 2}O{sub 3} powder and nano-size SiO{sub 2} as main raw materials. The sample was characterized by phase analysis, densification and thermal shock times. Moreover, field emission scanning electron microscope was also conducted to study microstructure of the samples before and after thermal shock. Effect of different molar ratios of MgO/Al{sub 2}O{sub 3} on the sintering behavior and thermal shock resistance of composite ceramics were investigated. The results showed that the sample possess better sintering behavior and thermal shock resistance with the molar ratio of MgO/Al{sub 2}O{sub 3} equal to 2/1. Grains of periclase and spinel were directly bonded together, resulting in a dense and compact microstructure, and the bulk density of obtained sample reached 3.4 g/cm{sup 3}. The microstructure of sample after thermal shock revealed that the crack propagation path was deflected and bifurcated, the main-crack propagation was restricted and more fracture energy was consumed, the thermal shock resistance of composite ceramics was greatly improved. - Highlights: • Effect of MgO/Al{sub 2}O{sub 3} on the composite ceramic was firstly researched with 1 mol% SiO{sub 2}. • Microcracks for a short distance by interlinking can eliminate the crack propagation. • The composite ceramic have optimal synthetic property with MgO/Al{sub 2}O{sub 3} was 2/1.

Exploring the possibility to store the mixed oxygen-hydrogen cluster in clathrate hydrate in molar ratio 1:2 (O2+2H2).

Science.gov (United States)

Qin, Yan; Du, Qi-Shi; Xie, Neng-Zhong; Li, Jian-Xiu; Huang, Ri-Bo

2017-05-01

An interesting possibility is explored: storing the mixture of oxygen and hydrogen in clathrate hydrate in molar ratio 1:2. The interaction energies between oxygen, hydrogen, and clathrate hydrate are calculated using high level quantum chemical methods. The useful conclusion points from this study are summarized as follows. (1) The interaction energies of oxygen-hydrogen mixed cluster are larger than the energies of pure hydrogen molecular cluster. (2) The affinity of oxygen molecules with water molecules is larger than that of the hydrogen molecules with water molecules. (3) The dimension of O 2 -2H 2 interaction structure is smaller than the dimension of CO 2 -2H 2 interaction structure. (4) The escaping energy of oxygen molecules from the hydrate cell is larger than that of the hydrogen molecules. (5) The high affinity of the oxygen molecules with both the water molecules and the hydrogen molecules may promote the stability of oxygen-hydrogen mixture in the clathrate hydrate. Therefore it is possible to store the mixed (O 2 +2H 2 ) cluster in clathrate hydrate. Copyright © 2017 Elsevier Inc. All rights reserved.

Structural characterization of the CeO{sub 2}/Gd{sub 2}O{sub 3} mixed system by synchrotron X-ray diffraction

Energy Technology Data Exchange (ETDEWEB)

Artini, Cristina, E-mail: c.artini@ge.ieni.cnr.it [Dipartimento di Chimica e Chimica Industriale, Universita degli Studi di Genova, Via Dodecaneso 31, 16146 Genova (Italy); Costa, Giorgio A., E-mail: costa@chimica.unige.it [Dipartimento di Chimica e Chimica Industriale, Universita degli Studi di Genova, Via Dodecaneso 31, 16146 Genova (Italy); CNR-SPIN Genova, Corso Perrone 24, 16152 Genova (Italy); Pani, Marcella, E-mail: marcella@chimica.unige.it [Dipartimento di Chimica e Chimica Industriale, Universita degli Studi di Genova, Via Dodecaneso 31, 16146 Genova (Italy); Lausi, Andrea, E-mail: andrea.lausi@elettra.trieste.it [Sincrotrone Trieste S.C.p.A., ss 14, km 163, 5, 34149 Basovizza, Trieste (Italy); Plaisier, Jasper, E-mail: jasper.plaisier@elettra.trieste.it [Sincrotrone Trieste S.C.p.A., ss 14, km 163, 5, 34149 Basovizza, Trieste (Italy)

2012-06-15

The structural determination of the CeO{sub 2}/Gd{sub 2}O{sub 3} mixed system is a non-trivial problem because of the close resemblance between the ionic sizes of Ce{sup 4+} and Gd{sup 3+} and between the crystal structures of CeO{sub 2} and Gd{sub 2}O{sub 3}. (Ce{sub 1-x}Gd{sub x})O{sub 2-x/2} powder samples with x ranging between 0 and 1 have been synthesized by coprecipitation of mixed oxalates and subsequent thermal decomposition in air at 1200 Degree-Sign C followed by slow cooling. Synchrotron powder X-ray diffraction data were collected and refined by the Rietveld method. Lattice parameters do not follow Vegard's law and no peak splitting has been observed for any composition, meaning that no biphasic regions exist over the whole compositional range. The same hybrid structural model - a proper mixture of the structures of the two pure oxides - was used for the refinements, allowing to account for the data observed. - graphical abstract: Substituting Ce{sup 4+} by Gd{sup 3+}, a gradual transition from the F structure (typical of CeO{sub 2}) to the C structure (typical of Gd{sub 2}O{sub 3}) takes place. The lattice parameters do not follow Vegard's law. Highlights: Black-Right-Pointing-Pointer A structural study of Ce-Gd mixed oxides has been performed. Black-Right-Pointing-Pointer In (Ce{sub 1-x}Gd{sub x})O{sub 2-x/2} a solid solution forms for 0{<=}x{<=}0.3. Black-Right-Pointing-Pointer For x>0.3 a gradual transition from the C to the F structure is observed. Black-Right-Pointing-Pointer Lattice parameters do not follow Vegard's law.

Nuclear fuel technology - Determination of the O/M ratio in MOX pellets - Gravimetric method

International Nuclear Information System (INIS)

2008-01-01

This International Standard describes a method for determining the oxygen-to-metal (O/M) ratio in mixed uranium-plutonium oxide pellets. The (U,Pu)O 2 x sample is submitted to controlled oxidation-reduction under thermodynamic conditions designed to change the O/M ratio to a value of 2,000. The initial stoichiometric deviation, X, is determined from the sample mass difference before and after heat treatment

Ordered Fe(II)Ti(IV)O3 Mixed Monolayer Oxide on Rutile TiO2(011).

Science.gov (United States)

Halpegamage, Sandamali; Ding, Pan; Gong, Xue-Qing; Batzill, Matthias

2015-08-25

Oxide monolayers supported or intermixed with an oxide support are potential nanocatalysts whose properties are determined by the interplay with the support. For fundamental studies of monolayer oxides on metal oxide supports, well-defined systems are needed, but so far, the synthesis of monolayer oxides with long-range order on single-crystal oxide surfaces is rare. Here, we show by a combination of scanning tunneling microscopy, photoemission spectroscopy, and density functional theory (DFT)-based computational analysis that the rutile TiO2(011) surface supports the formation of an ordered mixed FeTiO3 monolayer. Deposition of iron in a slightly oxidizing atmosphere (10(-8) Torr O2) and annealing to 300 °C results in a well-ordered surface structure with Fe in a 2+ charge state and Ti in a 4+ charge states. Low-energy ion scattering suggests that the cation surface composition is close to half Fe and half Ti. This surface is stable in ultrahigh vacuum to annealing temperatures of 300 °C before the iron is reduced. DFT simulations confirm that a surface structure with coverage of 50% FeO units is stable and forms an ordered structure. Although distinct from known bulk phases of the iron-titanium oxide systems, the FeTiO3 monolayer exhibits some resemblance to the ilmenite structure, which may suggest that a variety of different mixed oxide phases (of systems that exist in a bulk ilmenite phase) may be synthesized in this way on the rutile TiO2(011) substrate.

Effect of composition on properties of In2O3-Ga2O3 thin films

Science.gov (United States)

Demin, I. E.; Kozlov, A. G.

2017-06-01

The In2O3-Ga2O3 mixed oxide polycrystalline thin films with various ratios of components were obtained by pulsed laser deposition. The effect of films composition on surface morphology, electrophysical and gas sensing properties and energies of adsorption and desorption of combustible gases was studied. The films with50%In2O3-50%Ga2O3 composition showed maximum gas response (˜25 times) combined with minimum optimal working temperature (˜530 °C) as compared with the other films. The optical transmittance of the films in visible range was investigated. For 50%In2O3-50%Ga2O3 films, the transmittance is higher in comparison with the other films. The explanation of the dependency of films behaviors on their composition was presented.The In2O3-Ga2O3 films were assumed to have perspectives as gas sensing material for semiconducting gas sensors.

Application of silver vanadate solid electrolyte mixed with Al2O3 in Ag/I2 batteries

International Nuclear Information System (INIS)

Abdul Karim bin Arof.

1993-01-01

The glassy silver vanadate electrolyte of the composition 70AgI-20Ag20-10V205 was added with Al2O3 in varying percentages to form several physical mixtures that will be used to fabricate several solid stare electrochemical cells in order to study the influence of the dispersoid on the silver vanadate cells internal resistance and lifetime of the silver vanadate cells. The internal resistance of the cells increased on addition of Al2O3 but the cell with the mixture of Al2O3 and electrolyte in the weight ratio 2:3 has the lowest internal resistance. The increase in the internal resistance of the cell is attributed to the insulating nature of Al2O3. Although the internal resistance of the cell increased, it was observed that the time needed for the cell potential to drop to 400 mV at a constant discharge current of 30 uA increase in discharge lifetime was also observed when a second cell of the same mixed electrolyte constituents was discharged at 40 uA current drain. We have attempted to explain the increase in discharge lifetime in terms of the space charge layer developed between the insulator and the ionic conductor which results in a dipole region across which a potential difference is developed. This potential difference is responsible in prolonging the discharge lifetime of the cells

Convective mixing length and the galactic carbon to oxygen ratio

Energy Technology Data Exchange (ETDEWEB)

Serrano, A; Peimbert, M [Universidad Nacional Autonoma de Mexico, Mexico City. Inst. de Astronomia

1981-01-01

We have studied chemical evolution models, assuming instantaneous recycling, and considering: a) the effects of mass loss both in massive stars and in intermediate mass stars, and b) the initial mass function of the solar neighbourhood (Serrano 1978). From these models we have derived the yields of carbon and oxygen. It is concluded that the condition C/O approximately 0.58 in the solar neighbourhood can only be satisfied if, during advanced stages of stellar evolution of intermediate mass stars, the ratio of the convective mixing length to the pressure scale height is > approximately 2.

Influence of the Mixing Ways of Reactants on ZnO Morphology

Directory of Open Access Journals (Sweden)

Lining Yang

2013-01-01

Full Text Available ZnO particles with various morphologies were synthesized by mixing ZnSO4 and NaOH solutions at 25°C followed by aging of the suspensions at 40–80°C for 2.0 h, keeping the initial molar ratio of Zn2+ to OH− at 1 : 4. ZnO irregular plates were prepared by adding NaOH to ZnSO4 while ε-Zn(OH2 rhombic particles were produced using the opposite mixing way. After aging of the slurries at 80°C for 2.0 h, the ZnO plates were kept stable while the ε-Zn(OH2 rhombic particles were converted to ZnO whiskers with a length of 1.0–4.0 μm and a diameter of 0.03–0.3 μm. Thermodynamic analysis indicated that the formation of the Zn-bearing precipitates (ZnO or ε-Zn(OH2 at room temperature was connected closely with the solution composition.

Structural and optical properties of ZnO–SnO{sub 2} mixed thin films deposited by spray pyrolysis

Energy Technology Data Exchange (ETDEWEB)

Tharsika, T., E-mail: tharsika@siswa.um.edu.my; Haseeb, A.S.M.A., E-mail: haseeb@um.edu.my; Sabri, M.F.M., E-mail: faizul@um.edu.my

2014-05-02

Nanocrystalline ZnO–SnO{sub 2} mixed thin films were deposited by the spray pyrolysis technique at various substrate temperatures during deposition. The mixed films were prepared in the range of 20.9 at.% to 73.4 at.% by altering the Zn/(Sn + Zn) atomic ratio in the starting solution. Morphology, crystal structures, and optical properties of the films were characterized by field-emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), and ultraviolet–visible and photoluminescence (PL) spectroscopy. XRD analysis reveals that the crystallinity of the Sn-rich mixed thin films increases with increasing substrate temperatures. FESEM images show that the grain size of mixed thin films is smaller compared to that of pure ZnO and SnO{sub 2} thin films. A drop in the thickness and optical bandgap of the film was observed for films fabricated at high temperatures, which coincided with the increased crystallinity of the films. The average optical transmission of mixed thin films increased from 70% to 95% within the visible range (400–800 nm) as the substrate temperature increases. Optical bandgap of the films was determined to be in the range of 3.21–3.96 eV. The blue shift in the PL spectra from the films was supported by the fact that grain size of the mixed thin films is much smaller than that of the pure ZnO and SnO{sub 2} thin films. Due to the improved transmission and reduced grain size, the ZnO–SnO{sub 2} mixed thin films can have potential use in photovoltaic and gas sensing applications. - Highlights: • ZnO–SnO{sub 2} mixed thin films were deposited on glass substrate by spray pyrolysis. • Crystallinity of the thin films increases with substrate temperature. • Grain size of the mixed thin films is smaller than that of the pure thin films. • Reduction of grain size depends on mixed atomic ratios of precursor solution. • Optical band gap of films could be engineered by changing substrate temperature.

Enhanced performance of P3HT/(PCBM:ZnO:TiO{sub 2}) blend based hybrid organic solar cells

Energy Technology Data Exchange (ETDEWEB)

Ikram, M., E-mail: mianraj.1981@gmail.com [Solar Application Lab, Department of Physics, Government College University Lahore, 54000 Pakistan (Pakistan); Murray, R. [Department of Physics and Astronomy, University of Delaware, Delaware 19716 (United States); Imran, M. [Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, 29 Zhongguancun East Road, Haidian District, Beijing 100190 (China); Ali, S. [Solar Application Lab, Department of Physics, Government College University Lahore, 54000 Pakistan (Pakistan); Shah, S.Ismat [Department of Materials Science and Engineering, University of Delaware, Delaware 19716 (United States); Department of Physics and Astronomy, University of Delaware, Delaware 19716 (United States)

2016-03-15

Highlights: • We fabricated hybrid bulk heterojunction organic solar cells. • TiO{sub 2} and ZnO nanoparticles replace PCBM with fixed amount of P3HT in active layer • PCE was significantly improved by the introduction of TiO{sub 2} and ZnO. • A possible route toward low-cost OPV. • To the best of my knowledge, this work is the first time going to report. - Abstract: Quaternary blend hybrid organic solar cells enjoy both an increased light absorption range and an easy method to fabricate because of the simple structure. In this study effects of mixing inorganic metal oxides (ZnO and TiO{sub 2}) nanoparticles to the active layer of organic photovoltaics devices were investigated. The active layer primarily consists of various ratios of electron donor poly (3-hexylthiophene) (P3HT) and an electron acceptor [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) together with nanostructured ZnO and TiO{sub 2} dispersed in chlorobenzene (CB) and 1,2-dichlorobenzene (DCB). The ratio of PCBM to nanoparticles was varied keeping the ratio of P3HT to acceptor material constant. Mixing of nanoparticle plays a significant role in the resulting power conversion efficiency (PCE) of the devices. An increased PCE for ZnO/TiO{sub 2} doped devices can be attributed to increased absorption in the visible region and enhanced charge collection due to the percolation networks formed by metal oxides nanoparticles.

Properties measurements of (U{sub 0.7}Pu{sub 0.3})O{sub 2-x} in PO{sub 2}-controlled atmosphere

Energy Technology Data Exchange (ETDEWEB)

Kato, M.; Murakami, T.; Sunaoshi, T. [Advanced Nuclear System Research and Development Directorate, Japan Atomic Energy Agency, Muramatsu Tokai-mura Ibaraki, 319-1194 (Japan); Nelson, A.T.; McClellan, K.J. [Los Alamos National Laboratory, Los Alamos, New Mexico 87545 (United States)

2013-07-01

The investigation of physical properties of uranium and plutonium mixed oxide (MOX) fuels is important for the development of fast reactor fuels. It is well known that MOX is a nonstoichiometric oxide, and the physical properties change drastically with the Oxygen-to-Metal (O/M) ratio. A control technique for O/M ratio was established for measurements of high temperature properties of uranium and plutonium mixed oxide fuels. Sintering behavior, thermal expansion and O/M change of (U{sub 0.7}Pu{sub 0.3})O{sub 2.00} and (U{sub 0.7}Pu{sub 0.3})O{sub 1.99} were investigated in PO{sub 2}-controlled atmosphere which was controlled by H{sub 2}/H{sub 2}O gas system. Sintering behavior changed drastically with O/M ratio, and shrinkage of (U{sub 0.7}Pu{sub 0.3})O{sub 2.00} was faster and more advanced at lower temperatures as compared with (U{sub 0.7}Pu{sub 0.3})O{sub 1.99}. Thermal expansion was observed to be slightly increased with decreasing O/M ratio. (authors)

Influence of oxygen-metal ratio on mixed-oxide fuel performance

International Nuclear Information System (INIS)

Lawrence, L.A.; Leggett, R.D.

1979-04-01

The fuel oxygen-to-metal ratio (O/M) is recognized as an important consideration for performance of uranium--plutonium oxide fuels. An overview of the effects of differing O/M's on the irradiation performance of reference design mixed-oxide fuel in the areas of chemical and mechanical behavior, thermal performance, and fission gas behavior is presented. The pellet fuel has a nominal composition of 75 wt% UO 2 + 25 wt% PuO 2 at a pellet density of approx. 90% TD. for nominal conditions this results in a smeared density of approx. 85%. The cladding in all cases is 20% CW type 316 stainless steel with an outer diameter of 5.84 to 6.35 mm. O/M has been found to significantly influence fuel pin chemistry, mainly FCCI and fission product and fuel migration. It has little effect on thermal performance and overall mechanical behavior or fission gas release. The effects of O/M (ranging from 1.938 to 1.984) in the areas of fuel pin chemistry, to date, have not resulted in any reduction in fuel pin performance capability to goal burnups of approx. 8 atom% or more

Density-ratio effects on buoyancy-driven variable-density turbulent mixing

Science.gov (United States)

Aslangil, Denis; Livescu, Daniel; Banerjee, Arindam

2017-11-01

Density-ratio effects on the turbulent mixing of two incompressible, miscible fluids with different densities subject to constant acceleration are studied by means of high-resolution Direct Numerical Simulations. In a triply periodic domain, turbulence is generated by stirring in response to the differential buoyancy forces within the flow. Later, as the fluids become molecularly mixed, dissipation starts to overcome turbulence generation by bouyancy. Thus, the flow evolution includes both turbulence growth and decay, and it displays features present in the core region of the mixing layer of the Rayleigh-Taylor as well as Richtmyer-Meshkov instabilities. We extend the previous studies by investigating a broad range of density-ratio, from 1-14.4:1, corresponding to Atwood numbers of 0.05-0.87. Here, we focus on the Atwood number dependence of mixing-efficiency, that is defined based on the energy-conversion ratios from potential energy to total and turbulent kinetic energies, the decay characteristics of buoyancy-assisted variable-density homogeneous turbulence, and the effects of high density-ratios on the turbulence structure and mixing process. Authors acknowledge financial support from DOE-SSAA (DE-NA0003195) and NSF CAREER (#1453056) awards.

In situ trace gas and particle measurements in the summer lower stratosphere during STREAM II. Implications for O{sub 3} production

Energy Technology Data Exchange (ETDEWEB)

Bregman, A; Lelieveld, J; Scheeren, H A [Institute for Marine and Atmospheric Sciences, Utrecht (Netherlands); Arnold, F; Buerger, V; Schneider, J [Max-Planck-Inst. for Nuclear Physics, Heidelberg (Germany); Fischer, H; Waibel, A [Max-Planck-Inst. fuer Chemie, Mainz (Germany); Siegmund, P C; Wauben, W M.F. [Koninklijk Nederlands Meteorologisch Inst., De Bilt (Netherlands); Stroem, J [Stockholm Univ. (Sweden). Dept. of Meteorology

1998-12-31

In situ aircraft measurements of O{sub 3}, CO, HNO{sub 3}, and aerosol particles are presented, performed over the North Sea region in the summer lower stratosphere during the STREAM-II campaign (Stratosphere Troposphere Experiments by Aircraft Measurements). Elevated CO mixing ratios are attributed to mixing of polluted tropospheric air into the lowermost extra-tropical stratosphere. Model calculations illustrate that the O{sub 3} production efficiency of NO{sub x} is smaller than previously assumed, under conditions with relatively high HNO{sub 3} mixing ratios, as observed during STREAM-II. The model simulations further suggest a relatively high O{sub 3} production efficiency from CO oxidation, as a result of the relatively high ambient HNO{sub 3} and NO{sub x} concentrations, implying that upward transport of CO rich air enhances O{sub 3} production in the lowermost stratosphere. (author) 13 refs.

In situ trace gas and particle measurements in the summer lower stratosphere during STREAM II. Implications for O{sub 3} production

Energy Technology Data Exchange (ETDEWEB)

Bregman, A.; Lelieveld, J.; Scheeren, H.A. [Institute for Marine and Atmospheric Sciences, Utrecht (Netherlands); Arnold, F.; Buerger, V.; Schneider, J. [Max-Planck-Inst. for Nuclear Physics, Heidelberg (Germany); Fischer, H.; Waibel, A. [Max-Planck-Inst. fuer Chemie, Mainz (Germany); Siegmund, P.C.; Wauben, W.M.F. [Koninklijk Nederlands Meteorologisch Inst., De Bilt (Netherlands); Stroem, J. [Stockholm Univ. (Sweden). Dept. of Meteorology

1997-12-31

In situ aircraft measurements of O{sub 3}, CO, HNO{sub 3}, and aerosol particles are presented, performed over the North Sea region in the summer lower stratosphere during the STREAM-II campaign (Stratosphere Troposphere Experiments by Aircraft Measurements). Elevated CO mixing ratios are attributed to mixing of polluted tropospheric air into the lowermost extra-tropical stratosphere. Model calculations illustrate that the O{sub 3} production efficiency of NO{sub x} is smaller than previously assumed, under conditions with relatively high HNO{sub 3} mixing ratios, as observed during STREAM-II. The model simulations further suggest a relatively high O{sub 3} production efficiency from CO oxidation, as a result of the relatively high ambient HNO{sub 3} and NO{sub x} concentrations, implying that upward transport of CO rich air enhances O{sub 3} production in the lowermost stratosphere. (author) 13 refs.

Twin-cuvette measurement technique for investigation of dry deposition of O3 and PAN to plant leaves under controlled humidity conditions

Directory of Open Access Journals (Sweden)

S. Sun

2016-02-01

with Quercus ilex was investigated over a 14 day measurement period under controlled climate chamber conditions. By using O3 mixing ratios between 32 and 105 ppb and PAN mixing ratios between 100 and 350 ppt, a linear dependency of the O3 flux as well as the PAN flux in relation to its ambient mixing ratio could be observed. At relative humidity (RH of 40 %, the deposition velocity ratio of O3 and PAN was determined to be 0.45. At that humidity, the deposition of O3 to the plant leaves was found to be only controlled by the leaf stomata. For PAN, an additional resistance inhibited the uptake of PAN by the leaves. Furthermore, the formation of water films on the leaf surface of plants inside the chamber could be continuously tracked with our custom built leaf wetness sensors. Using this modified leaf wetness sensor measuring the electrical surface conductance on the leaves, an exponential relationship between the ambient humidity and the electrical surface conductance could be determined.

Aqueous suspensions of {alpha}Al{sub 2}O{sub 3}/SiC mixed systems

Energy Technology Data Exchange (ETDEWEB)

Pagnoux, C.; Baklouti, S.; Chartier, T.; Baumard, J.F. [ENSCI, Limoges (France). LMCTS

1997-12-31

The preparation of aqueous {alpha}-Al{sub 2}O{sub 3}, {alpha}-SiO{sub 2} and {alpha}-SiC suspensions with polyelectrolytes, respectively the NH{sub 4}{sup +} salt of polymethacrylic acid (PMA-NH{sub 4}{sup +}) and acidic form polyethylene imine (PEI-H{sup +}) is investigated. It is based on the adsorption of these polyelectrolytes which in turn depends mainly on the nature of the polyelectrolyte, and the charge density which develops on the powder surface in water. Good dispersion and stability of dispersions are then obtained through electrostatic and steric stabilization. As an application, the preparation of an Al{sub 2}O{sub 3}-SiC aqueous mixed slurry was investigated as a preliminary step for processing of Al{sub 2}O{sub 3}/SiC nanocomposites. (orig.) 2 refs.

Oxygen-to-metal ratio control during fabrication of mixed oxide fast breeder reactor fuel pellets

International Nuclear Information System (INIS)

Rasmussen, D.E.; Benecke, M.W.; Jentzen, W.R.; McCord, R.B.

1979-05-01

Oxygen-to-metal ratio (O/M) of mixed oxide fuel pellets can be controlled during fabrication by proper selection of binder (type and content) and sintering conditions. Sintering condition adjustments involved the passing of Ar--8% H 2 sintering gas across a cryostat ice bath controlled to temperatures ranging from -5 to -60 0 C to control as-sintered pellet O/M ratio. As-sintered fuel pellet O/M decreased with increasing Sterotex binder and PuO 2 concentrations, increasing sintering temperature, and decreasing sintering gas dew point. Approximate relationships between Sterotex binder level and O/M were established for PuO 2 --UO 2 and PuO 2 --ThO 2 fuels. O/M was relatively insensitive to Carbowax binder concentration. Several methods of increasing O/M using post-sintering pellet heat treatments were demonstrated, with the most reliable being a two-step process of first raising the O/M to 2.00 (stoichiometric) at 650 0 C in Ar--8% H 2 bubbled through H 2 O, followed by hydrogen reduction to specification O/M in oxygen-gettered Ar-8% H 2 at temperatures ranging from 1200 to 1690 0 C

The effect of B_2O_3 flux on growth NLBCO superconductor by solid state reaction and wet-mixing methods

International Nuclear Information System (INIS)

Suharta, W. G.; Wendri, N.; Ratini, N.; Suarbawa, K. N.

2016-01-01

The synthesis of B_2O_3 flux substituted NLBCO superconductor NdBa_1_._7_5La_0_._2_5Cu_3O_7_-_∂ has been done using solid state reaction and wet-mixing methods in order to obtain homogeneous crystals and single phase. From DTA/TGA characteritations showed the synthesis process by wet-mixing requires a lower temperature than the solid state reaction in growing the superconductor NdBa_1_._7_5La_0_._2_5Cu_3O_7_-_∂. Therefore, in this research NdBa_1_._7_5La_0_._2_5Cu_3O_7_-_∂ sample calcinated at 650°C for wet-mixing method and 820°C for solid state reaction methods. The all samples was sintered at 950°C for ten hours. Crystallinity of the sample was confirmed using X-ray techniques and generally obtained sharp peaks that indicates the sample already well crystallized. Search match analyses for diffraction data gave weight fractions of impurity phase of the solid state reaction method higher than wet-mixing method. In this research showed decreasing the price of the lattice parameter about 1% with the addition of B_2O_3 flux for the both synthesis process and 2% of wet mixing process for all samples. Characterization using scanning electron microscopy (SEM) showed the distribution of crystal zise for wet-mixing method more homogeneous than solid state reaction method, with he grain size of samples is around 150–250 nm. The results of vibrating sample magnetometer (VSM) showed the paramagnetic properties for all samples.

Effect of methanol ratio in mixed solvents on optical properties and wettability of ZnO films by cathodic electrodeposition

International Nuclear Information System (INIS)

Zhang, Miao; Xu, Kai; Jiang, Xishun; Yang, Lei; He, Gang; Song, Xueping; Sun, Zhaoqi; Lv, Jianguo

2014-01-01

Highlights: • Different surface morphologies of ZnO films were prepared by cathodic electrodeposition. • The surface morphologies are controlled through add different ratio methanol to electrolyte. • The morphology changes from nanorods with hexagonal structure to net-like nanostructure. • The wettability of films shows obvious change with increasing methanol ratio. • The maximum light-induced CA change has been observed with the methanol ratio of 0.8. - Abstract: ZnO thin films were prepared in the electrolyte with different methanol ratio by cathodic electrodeposition method. Microstructure, surface morphology, optical properties and wettability of the thin films were investigated by X-ray diffractometer, field-emission scanning electron microscope, ultraviolet–visible spectroscope, fluorescence spectrometer and water contact angle apparatus. Increase of methanol ratio in the solvents may restrain the (0 0 2) plane preferential orientation in some extent. Change of current density curves with the ratio of methanol in the solution play a vital role on electrochemical reaction kinetics, microstructure and/or surface morphology of ZnO thin films. With the methanol ratio increase from 0 to 0.8, the surface morphology changes from nanorods to net-like nanostructure. The adsorbed NO 3 − ions on the polar planes hinder the crystal growth along the c-axis and redirect the growth direction along the nonpolar planes. The maximum and minimum band gaps have been obtained in the ZnO thin films with the methanol ratio of 0.4 and 0.6, respectively. Change of contact angle before UV irradiation may be related to surface morphology and oxygen vacancies. The maximum light-induced water contact angle change has been observed in the sample with the methanol ratio of 0.8. The results may be attributed to the higher surface roughness and net-like morphology

Effect of methanol ratio in mixed solvents on optical properties and wettability of ZnO films by cathodic electrodeposition

Energy Technology Data Exchange (ETDEWEB)

Zhang, Miao; Xu, Kai; Jiang, Xishun; Yang, Lei; He, Gang; Song, Xueping [School of Physics and Material Science, Anhui University, Hefei 230601 (China); Sun, Zhaoqi, E-mail: szq@ahu.edu.cn [School of Physics and Material Science, Anhui University, Hefei 230601 (China); Lv, Jianguo, E-mail: lvjg1@163.com [School of Electronic and Information Engineering, Hefei Normal University, Hefei 230601 (China)

2014-12-05

Highlights: • Different surface morphologies of ZnO films were prepared by cathodic electrodeposition. • The surface morphologies are controlled through add different ratio methanol to electrolyte. • The morphology changes from nanorods with hexagonal structure to net-like nanostructure. • The wettability of films shows obvious change with increasing methanol ratio. • The maximum light-induced CA change has been observed with the methanol ratio of 0.8. - Abstract: ZnO thin films were prepared in the electrolyte with different methanol ratio by cathodic electrodeposition method. Microstructure, surface morphology, optical properties and wettability of the thin films were investigated by X-ray diffractometer, field-emission scanning electron microscope, ultraviolet–visible spectroscope, fluorescence spectrometer and water contact angle apparatus. Increase of methanol ratio in the solvents may restrain the (0 0 2) plane preferential orientation in some extent. Change of current density curves with the ratio of methanol in the solution play a vital role on electrochemical reaction kinetics, microstructure and/or surface morphology of ZnO thin films. With the methanol ratio increase from 0 to 0.8, the surface morphology changes from nanorods to net-like nanostructure. The adsorbed NO{sub 3}{sup −} ions on the polar planes hinder the crystal growth along the c-axis and redirect the growth direction along the nonpolar planes. The maximum and minimum band gaps have been obtained in the ZnO thin films with the methanol ratio of 0.4 and 0.6, respectively. Change of contact angle before UV irradiation may be related to surface morphology and oxygen vacancies. The maximum light-induced water contact angle change has been observed in the sample with the methanol ratio of 0.8. The results may be attributed to the higher surface roughness and net-like morphology.

Fabrication of high aspect ratio TiO2 and Al2O3 nanogratings by atomic layer deposition

DEFF Research Database (Denmark)

Shkondin, Evgeniy; Takayama, Osamu; Michael-Lindhard, Jonas

2016-01-01

The authors report on the fabrication of TiO2 and Al2O3 nanostructured gratings with an aspect ratio of up to 50. The gratings were made by a combination of atomic layer deposition (ALD) and dry etch techniques. The workflow included fabrication of a Si template using deep reactive ion etching...... spectroscopy. The approach presented opens the possibility to fabricate high quality optical metamaterials and functional nanostructures....

Antibacterial activity against Escherichia coli and characterization of ZnO and ZnO–Al2O3 mixed oxide nanoparticles

Directory of Open Access Journals (Sweden)

Ertan Şahin

2017-02-01

Full Text Available In order to achieve better antibacterial water insoluble nanoparticles (Nanoparticles of ZnO and ZnO–Al2O3 were studied. ZnO–Al2O3 mixed oxide nanoparticles were produced from a solution containing Zn(AC2⋅2H2O and AlCl3 by Solvothermal method. The calcination process of the ZnO–Al2O3 composite nanoparticles brought forth polycrystalline one phase ZnO–Al2O3 nanoparticles of 30–50 nm in diameters. ZnO and ZnO–Al2O3 were crystallized into würtzite and rock salt structures, respectively. The structural properties of this sample were analyzed by XRD and compared with bulk case of these samples. Antibacterial effectiveness of the ZnO and ZnO–Al2O3 nanoparticles were tested against general Escherichia coli (E. coli ATCC 25922 and E. coli O157:H7 by measuring the growth through optical density and digital counting of live–dead cells. Minimum inhibitory concentration values against four representative bacteria along with E. coli O157:H7 were also obtained.

Effect of [Li]/[Nb] ratio on composition and defect structure of Zr:Yb:Tm:LiNbO3 crystals

Science.gov (United States)

Liu, Chunrui; Dai, Li; Wang, Luping; Shao, Yu; Yan, Zhehua; Xu, Yuheng

2018-04-01

Zr:Yb:Tm:LiNbO3 crystals with various [Li]/[Nb] ratios (0.946, 1.05, 1.20 and 1.38) were grown by the Czochralski technique. Distribution coefficients of Zr4+, Yb3+ and Tm3+ ions were analyzed by the inductively coupled plasma-atomic emission spectrometer (ICP-AES). The influence of [Li]/[Nb] ratio on the composition and defect structure of Zr:Yb:Tm:LiNbO3 crystals was investigated by X-ray diffraction and IR transmission spectrum. The results show that as the [Li]/[Nb] ratio increases in the melt, the distribution coefficients of Yb3+ and Tm3+ ions both increase while that of Zr4+ ion deceases. When the [Li]/[Nb] ratio increases to 1.20 in the melt, Zr:Yb:Tm:LiNbO3 crystal is nearly stoichiometric. In addition, when the [Li]/[Nb] ratio reaches up to 1.38, NbLi4+ are completely replaced and Li+ starts to impel the Zr4+, Yb3+ and Tm3+ into the normal Li sites.

Measurements of the 18O/16O ratio of dissolved oxygen in the North Sea during FLEX 76

International Nuclear Information System (INIS)

Foerstel, H.; Zielke, H.

1978-01-01

In spring 1976 a special part of the North Sea was the subject of research by a group of international scientists in the so-called 'Fladenground Experiment 1976 (FLEX 76). The team participated aboard the research ship Planet in an attempt to study the oxygen exchange between sea and atmosphere and the mixing within the water column. The water samples were taken in a small area during a period of two weeks. The water depth did not exceed 140 m. The dissolved oxygen was extracted using a vacuum system, and stored after adsorption on a molecular sieve. In the laboratory the oxygen was burned to carbon dioxide and the 18 O/ 16 O ratio was determined with a mass spectrometer. At the surface the sea water was saturated with air and showed the 18 O/ 16 O ratio of atmospheric oxygen. Towards the deeper layers the oxygen was consumed, and as a result the heavier isotope 18 O was enriched. This enrichment can be seen in a very marked manner even in the upper 100 m of the sea. In our case the 18 O enrichment indicates that the mixing processes did not exchange the oxygen of the layers beneath the surface rapidly. (Auth.)

Retrieval of water vapor mixing ratios from a laser-based sensor

Science.gov (United States)

Tucker, George F.

1995-01-01

Langley Research Center has developed a novel external path sensor which monitors water vapor along an optical path between an airplane window and reflective material on the plane's engine. An infrared tunable diode laser is wavelength modulated across a water vapor absorption line at a frequency f. The 2f and DC signals are measured by a detector mounted adjacent to the laser. The 2f/DC ratio depends on the amount of wavelength modulation, the water vapor absorption line being observed, and the temperature, pressure, and water vapor content of the atmosphere. The present work concerns efforts to quantify the contributions of these factors and to derive a method for extracting the water vapor mixing ratio from the measurements. A 3 m cell was fabricated in order to perform laboratory tests of the sensor. Measurements of 2f/DC were made for a series of pressures and modulation amplitudes. During my 1994 faculty fellowship, a computer program was created which allowed 2f/DC to be calculated for any combination of the variables which effect it. This code was used to generate 2f/DC values for the conditions measured in the laboratory. The experimental and theoretical values agreed to within a few percent. As a result, the laser modulation amplitude can now be set in the field by comparing the response of the instrument to the calculated response as a function of modulation amplitude. Once the validity of the computer code was established, it was used to investigate possible candidate absorption lines. 2f/DC values were calculated for pressures, temperatures, and water vapor mixing ratios expected to be encountered in future missions. The results have been incorporated into a database which will be used to select the best line for a particular mission. The database will also be used to select a retrieval technique. For examples under some circumstances there is little temperature dependence in 2f/DC so temperature can be neglected. In other cases, there is a dependence

Uptake of methanol on mixed HNO3/H2O clusters: An absolute pickup cross section

Science.gov (United States)

Pysanenko, A.; Lengyel, J.; Fárník, M.

2018-04-01

The uptake of atmospheric oxidized organics on acid clusters is relevant for atmospheric new particle formation. We investigate the pickup of methanol (CH3OH) on mixed nitric acid-water clusters (HNO3)M(H2O)N by a combination of mass spectrometry and cluster velocity measurements in a molecular beam. The mass spectra of the mixed clusters exhibit (HNO3)m(H2O)nH+ series with m = 0-3 and n = 0-12. In addition, CH3OH.(HNO3)m(H2O)nH+ series with very similar patterns appear in the spectra after the methanol pickup. The velocity measurements prove that the undoped (HNO3)m(H2O)nH+ mass peaks in the pickup spectra originate from the neutral (HNO3)M(H2O)N clusters which have not picked up any CH3OH molecule, i.e., methanol has not evaporated upon the ionization. Thus the fraction of the doped clusters can be determined and the mean pickup cross section can be estimated, yielding σs ¯ ≈ 20 Å2. This is compared to the lower estimate of the mean geometrical cross section σg ¯ ≈ 60 Å2 obtained from the theoretical cluster geometries. Thus the "size" of the cluster corresponding to the methanol pickup is at least 3-times smaller than its geometrical size. We have introduced a method which can yield the absolute pickup cross sections relevant to the generation and growth of atmospheric aerosols, as illustrated in the example of methanol and nitric acid clusters.

Frictional properties of CeO$_{2}$-Al$_{2}$O$_{3}$-ZrO$_{2}$ plasma-sprayed film under mixed and boundary lubricating conditions

CERN Document Server

Kita, H; Osumi, K; 10.2109/jcersj.112.615

2004-01-01

In order to find a counterpart for reducing the frictional coefficient of Al/sub 2/O/sub 3/-ZrO/sub 2/-CeO/sub 2/ plasma-sprayed film, the sliding properties in mixed and boundary lubricating conditions was investigated. It was found that combination of a CrN- coated cast iron pin and an Al/sub 2/O/sub 3/-ZrO/sub 2/-CeO/sub 2/ plasma sprayed plate provided the lowest frictional coefficient among several combinations chosen from practical materials. The coefficient of friction was much lower than that of the materials combination widely used for piston ring and cylinder liner. It was inferred that the combination of a pin made of hard materials with high density, a smooth surface such as CrN-coated cast iron and a porous plate can reduce the frictional coefficient because less sliding resistance is implemented and porosity retains oil.

Atomic layer deposition and properties of mixed Ta2O5 and ZrO2 films

Directory of Open Access Journals (Sweden)

Kaupo Kukli

2017-02-01

Full Text Available Thin solid films consisting of ZrO2 and Ta2O5 were grown by atomic layer deposition at 300 °C. Ta2O5 films doped with ZrO2, TaZr2.75O8 ternary phase, or ZrO2 doped with Ta2O5 were grown to thickness and composition depending on the number and ratio of alternating ZrO2 and Ta2O5 deposition cycles. All the films grown exhibited resistive switching characteristics between TiN and Pt electrodes, expressed by repetitive current-voltage loops. The most reliable windows between high and low resistive states were observed in Ta2O5 films mixed with relatively low amounts of ZrO2, providing Zr to Ta cation ratio of 0.2.

Study of a Mixed Alkaline–Earth Effect on Some Properties of Glasses of the CaO-MgO-Al2O3-SiO2 System

Directory of Open Access Journals (Sweden)

Valle-Fuentes, J. F.

2007-06-01

Full Text Available In the present work, we studied a “Mixed Alkaline–Earth Effect”, i.e. the non-linear behaviour showed by the glass transition temperature as well as by the compressive strength of glasses of the CaO-MgO-Al2O3-SiO2 system, when a part of the CaO contained in them was substituted by a BaO/SrO mixture, in variable molar proportions. An important factor for the occurrence of this phenomenon was the difference in atomic weight, ionic radii and field strength of the Ba2+ and Sr2+ ions in comparison with those corresponding to the Ca2+ ion. Another factor considered was the likely occurrence of a microphase separation caused by the addition of BaO and/or SrO, together with the presence of F- and Mg2+ in the glasses. Other glass properties studied as a function of the CaO substitution level were density, glass molar volume, oxygen molar volume, packing fraction, and chemical resistance in neutral, basic and acidic aqueous media. In general, the structural reinforcement of the glass network caused by the partial substitution of CaO by a BaO/SrO mixture was accompanied by an improvement in the alkaline resistance of the materials, which were found to be suitable for applications in corrosive environments, especially in basic media. Keywords: Mixed alkaline–earth effect; CaO-MgO-Al2O3-SiO2 system; glass properties.En el presente trabajo, se estudia el comportamiento no lineal mostrado por la temperatura de transición vítrea y por la resistencia a la compresión de vidrios del sistema CaO-MgO-Al2O3-SiO2, cuando una parte del CaO contenido en los mismos es sustituido por una mezcla de BaO/SrO, en relación molar variable. Factores importantes para que se de este comportamiento son la diferencia entre pesos atómicos, radios iónicos e intensidad de campo de los iones Ba2+ y Sr2+ y los del propio ión Ca2+. Otro factor considerado ha sido la probable existencia de una separación de microfases originada por la adición de BaO y/o SrO, junto con la

Experimental study of isospin mixing in 12C + n → 13C(T = 3/2) and 16O + n → 17O(T = 3/2) resonances

International Nuclear Information System (INIS)

Cierjacks, S.; Schmalz, G.; Hinterberger, F.; Rossen, P. v.

1981-12-01

Narrow resonances of 13 C and 17 O have been studied by a measurement of the total neutron cross sections of carbon and oxygen between 3 and 30 MeV. Employing the improved time-of-flight spectrometer at the Karlsruhe Isochronous Cyclotron and precise calibration methods, resonance cross sections were measured with an energy resolution of 1:2100 at 10 MeV and energy accuracies between 10 -4 and 10 -5 . Resonance analysis of the measured data provided parameters for numerous narrow states of both isospins, T = 1/2 and T = 3/2. These data in conjunction with information from broad T = 1/2 resonances provided a good means to experimentally determine isospin mixing matrix elements. Results were obtained for the first five T = 3/2 resonances in 17 O and the first T = 3/2 resonance in 13 C. The obtained mixing matrix elements are compared with previous experimental results and shell-modell predictions of this quantity. (orig.) [de

Dry deposition of O_3 and SO_2 estimated from gradient measurements above a temperate mixed forest

International Nuclear Information System (INIS)

Wu, Zhiyong; Staebler, Ralf; Vet, Robert; Zhang, Leiming

2016-01-01

Vertical profiles of O_3 and SO_2 concentrations were monitored at the Borden Forest site in southern Ontario, Canada from May 2008 to April 2013. A modified gradient method (MGM) was applied to estimate O_3 and SO_2 dry deposition fluxes using concentration gradients between a level above and a level below the canopy top. The calculated five-year mean (median) dry deposition velocity (V_d) were 0.35 (0.27) and 0.59 (0.54) cm s"−"1, respectively, for O_3 and SO_2. V_d(O_3) exhibited large seasonal variations with the highest monthly mean of 0.68 cm s"−"1 in August and the lowest of 0.09 cm s"−"1 in February. In contrast, seasonal variations of V_d(SO_2) were smaller with monthly means ranging from 0.48 (May) to 0.81 cm s"−"1 (December). The different seasonal variations between O_3 and SO_2 were caused by the enhanced SO_2 uptake by snow surfaces in winter. Diurnal variations showed a peak value of V_d in early morning in summer months for both O_3 and SO_2. Canopy wetness increased the non-stomatal uptake of O_3 while decreasing the stomatal uptake. This also applied to SO_2, but additional factors such as surface acidity also played an important role on the overall uptake. - Highlights: • Application of a modified gradient-method for quantifying dry deposition is demonstrated. • A five-year dry deposition database is developed for O_3 and SO_2 over a mixed forest. • Canopy wetness enhances non-stomatal O_3 uptake while inhibits stomatal uptake. • High surface acidity reduces SO_2 dry deposition. - Capsule: A five-year dataset of O_3 and SO_2 dry deposition velocities was generated from concentration gradient measurement data using a modified gradient method.

Solid-solid interactions in Co3O4-MoO3/MgO system

International Nuclear Information System (INIS)

Radwan, Nagi R.E.; Ghozza, Ahmed M.; El-Shobaky, Gamil A.

2003-01-01

Cobalt/magnesium mixed oxide solids and cobalt-molybdenum/magnesium mixed oxide solids were prepared by thermal decomposition of basic magnesium carbonate pretreated with different proportions of cobalt nitrate and then with calculated amounts of ammonium molybdate. The proportions of cobalt expressed as Co 3 O 4 were 0.1, 0.2 and 0.3 mol while the concentrations of molybdenum expressed as mol% MoO 3 were 2.5 and 5.0. The prepared mixed solid specimens were calcined in air at 400-1000 deg. C. The solid-solid interactions in Co 3 O 4 -MoO 3 were investigated using DTA, TG and X-ray powder diffraction (XRD) techniques. The results obtained revealed that MgO dissolved cobalt oxide in its lattice forming CoO-MgO solid solution. The amount of cobalt dissolved increases by increasing the temperature in the range 800-1000 deg. C. This finding was confirmed by X-ray diffractograms in which all the diffraction lines of cobalt oxide disappeared at 1000 deg. C. MoO 3 present interacted readily with MgO and cobalt oxide by heat treatment at temperature starting from 400 deg. C producing MgMoO 4 and CoMoO 4 which remained stable by heating at 1000 deg. C. The impregnation of basic magnesium carbonate with cobalt nitrate much enhanced its thermal decomposition yielding MgO, which decomposed completely at 395.5 deg. C instead of 525 deg. C. The formation of magnesium cobaltite (MgCo 2 O 4 ) has been ruled out via XRD investigation at relatively high diffraction angles

Improved performance of solution-processed a-InGaZnO thin-film transistors due to Ar/O2 mixed-plasma treatment

International Nuclear Information System (INIS)

Kim, Kwan-Soo; Hwang, Yeong-Hyeon; Hwang, In-Chan; Cho, Won-Ju

2014-01-01

We investigated the effects of Ar and O 2 treatment and of Ar/O 2 mixed plasma treatment on the electrical characteristics of solution-processed amorphous indium-gallium-zinc-oxide (a-IGZO) thin-film transistors (TFTs). The electrical performance and the instability of a-IGZO TFTs were significantly improved by the plasma treatments. The plasma treatments reduced the carbon-based residual contamination that acted as possible trap sites. In particular, the O 2 -plasma treatment produced a significant improvement in the reliability of a-IGZO TFTs when compared with the Ar-plasma-treated device, owing to the elimination of residual carbon in the active channel of the solution-processed a-IGZO. However, the optimized improvement of the solution-processed a-IGZO TFT under a gate bias stress was obtained for the device treated with an Ar/O 2 mixed-gas plasma. The plasma treatment in the Ar/O 2 -mixed ambience remarkably enhanced not only the reliability but also the electrical performance of the a-IGZO TFT; the on/off-current ratio, the field-effect mobility, and the subthreshold slope were 6.78 x 10 7 , 1.24 cm 2 /V·s, and 513 mV/dec, respectively.

Experimental heat capacities, excess entropies, and magnetic properties of bulk and nano Fe3O4-Co3O4 and Fe3O4-Mn3O4 spinel solid solutions

Science.gov (United States)

Schliesser, Jacob M.; Huang, Baiyu; Sahu, Sulata K.; Asplund, Megan; Navrotsky, Alexandra; Woodfield, Brian F.

2018-03-01

We have measured the heat capacities of several well-characterized bulk and nanophase Fe3O4-Co3O4 and Fe3O4-Mn3O4 spinel solid solution samples from which magnetic properties of transitions and third-law entropies have been determined. The magnetic transitions show several features common to effects of particle and magnetic domain sizes. From the standard molar entropies, excess entropies of mixing have been generated for these solid solutions and compared with configurational entropies determined previously by assuming appropriate cation and valence distributions. The vibrational and magnetic excess entropies for bulk materials are comparable in magnitude to the respective configurational entropies indicating that excess entropies of mixing must be included when analyzing entropies of mixing. The excess entropies for nanophase materials are even larger than the configurational entropies. Changes in valence, cation distribution, bonding and microstructure between the mixing ions are the likely sources of the positive excess entropies of mixing.

Atmospheric ammonia mixing ratios at an open-air cattle feeding facility.

Science.gov (United States)

Hiranuma, Naruki; Brooks, Sarah D; Thornton, Daniel C O; Auvermann, Brent W

2010-02-01

Mixing ratios of total and gaseous ammonia were measured at an open-air cattle feeding facility in the Texas Panhandle in the summers of 2007 and 2008. Samples were collected at the nominally upwind and downwind edges of the facility. In 2008, a series of far-field samples was also collected 3.5 km north of the facility. Ammonium concentrations were determined by two complementary laboratory methods, a novel application of visible spectrophotometry and standard ion chromatography (IC). Results of the two techniques agreed very well, and spectrophotometry is faster, easier, and cheaper than chromatography. Ammonia mixing ratios measured at the immediate downwind site were drastically higher (approximately 2900 parts per billion by volume [ppbv]) than thos measured at the upwind site (open-air animal feeding operations, especially under the hot and dry conditions present during these measurements.

Diurnal variations in H{sub 2}O{sub 2}, O{sub 3}, PAN, HNO{sub 3} and aldehyde concentrations and NO/NO{sub 2} ratios at Rishiri Island, Japan: Potential influence from iodine chemistry

Energy Technology Data Exchange (ETDEWEB)

Kanaya, Yugo [Frontier Research Center for Global Change, Japan Agency for Marine-Earth Science and Technology, 3173-25 Showa-machi, Kanazawa-ku, Yokohama, Kanagawa 236-0001 (Japan)]. E-mail: yugo@jamstec.go.jp; Tanimoto, Hiroshi [National Institute for Environmental Studies, Tsukuba (Japan); Matsumoto, Jun [Integrated Research Institute, Tokyo Institute of Technology, Yokohama (Japan); Furutani, Hiroshi [Department of Chemistry and Biochemistry, University of California, San Diego (United States); Hashimoto, Shigeru [National Institute for Environmental Studies, Tsukuba (Japan); Komazaki, Yuichi [Frontier Research Center for Global Change, Japan Agency for Marine-Earth Science and Technology, 3173-25 Showa-machi, Kanazawa-ku, Yokohama, Kanagawa 236-0001 (Japan); Tanaka, Shigeru [Department of Applied Chemistry, Keio University, Yokohama (Japan); Yokouchi, Yoko [National Institute for Environmental Studies, Tsukuba (Japan); Kato, Shungo [Department of Applied Chemistry, Graduate School of Engineering, Tokyo Metropolitan University, Hachioji (Japan); Kajii, Yoshizumi [Department of Applied Chemistry, Graduate School of Engineering, Tokyo Metropolitan University, Hachioji (Japan); Akimoto, Hajime [Frontier Research Center for Global Change, Japan Agency for Marine-Earth Science and Technology, 3173-25 Showa-machi, Kanazawa-ku, Yokohama, Kanagawa 236-0001 (Japan)

2007-04-15

The presence of iodine chemistry, hypothesized due to the overprediction of HO{sub 2} levels by a photochemical box model at Rishiri Island in June 2000, was quantitatively tested against the observed NO/NO{sub 2} ratios and the net production rates of ozone. The observed NO/NO{sub 2} ratios were reproduced reasonably well by considering the conversion of NO to NO{sub 2} by IO, whose amount was calculated so as to reproduce the observed HO{sub 2} levels. However, the net production rates of ozone were calculated to be negative when such high mixing ratios of IO were considered, which was inconsistent with the observed buildup of ozone during daytime. These results suggest that iodine chemistry may not be the sole mechanism for the reduced mixing ratios of HO{sub 2}, or that 'hot spots' for iodine chemistry were present. Diurnal variations in the mixing ratios of HCHO, CH{sub 3}CHO, peroxy acetyl nitrate (PAN) and HNO{sub 3} observed during the study are presented along with the simulated ones. The box model simulations suggest that the effect of iodine chemistry on these concentrations is small and that important sources of CH{sub 3}CHO and sinks of PAN are probably missing from our current understanding of the tropospheric chemistry mechanism.

Characterization of Mixed xWO3(1-xY2O3 Nanoparticle Thick Film for Gas Sensing Application

Directory of Open Access Journals (Sweden)

M. H. Shahrokh Abadi

2010-05-01

Full Text Available Microstructural, topology, inner morphology, and gas-sensitivity of mixed xWO3(1-xY2O3 nanoparticles (x = 1, 0.95, 0.9, 0.85, 0.8 thick-film semiconductor gas sensors were studied. The surface topography and inner morphological properties of the mixed powder and sensing film were characterized with X-ray diffraction (XRD, atomic force microscopy (AFM, transmission electron microscopy (TEM, and scanning electron microscopy (SEM. Also, gas sensitivity properties of the printed films were evaluated in the presence of methane (CH4 and butane (C4H10 at up to 500 °C operating temperature of the sensor. The results show that the doping agent can modify some structural properties and gas sensitivity of the mixed powder.

Variable lifetimes and loss mechanisms for NO3 and N2O5 during the DOMINO campaign: contrasts between marine, urban and continental air

Science.gov (United States)

Crowley, J. N.; Thieser, J.; Tang, M. J.; Schuster, G.; Bozem, H.; Beygi, Z. H.; Fischer, H.; Diesch, J.-M.; Drewnick, F.; Borrmann, S.; Song, W.; Yassaa, N.; Williams, J.; Pöhler, D.; Platt, U.; Lelieveld, J.

2011-11-01

Nighttime mixing ratios of boundary layer N2O5 were determined using cavity-ring-down spectroscopy during the DOMINO campaign in Southern Spain (Diel Oxidant Mechanisms In relation to Nitrogen Oxides, 21 November 2008-8 December 2008). N2O5 mixing ratios ranged from below the detection limit (~5 ppt) to ~500 ppt. A steady-state analysis constrained by measured mixing ratios of N2O5, NO2 and O3 was used to derive NO3 lifetimes and compare them to calculated rates of loss via gas-phase and heterogeneous reactions of both NO3 and N2O5. Three distinct types of air masses were encountered, which were largely marine (Atlantic), continental or urban-industrial in origin. NO3 lifetimes were longest in the Atlantic sector (up to ~30 min) but were very short (a few seconds) in polluted, air masses from the local city and petroleum-related industrial complex of Huelva. Air from the continental sector was an intermediate case. The high reactivity to NO3 of the urban air mass was not accounted for by gas-phase and heterogeneous reactions, rates of which were constrained by measurements of NO, volatile organic species and aerosol surface area. In general, high NO2 mixing ratios were associated with low NO3 lifetimes, though heterogeneous processes (e.g. reaction of N2O5 on aerosol) were generally less important than direct gas-phase losses of NO3. The presence of SO2 at levels above ~2 ppb in the urban air sector was always associated with very low N2O5 mixing ratios indicating either very short NO3 lifetimes in the presence of combustion-related emissions or an important role for reduced sulphur species in urban, nighttime chemistry. High production rates coupled with low lifetimes of NO3 imply an important contribution of nighttime chemistry to removal of both NOx and VOC.

Variable lifetimes and loss mechanisms for NO3 and N2O5 during the DOMINO campaign: contrasts between marine, urban and continental air

Directory of Open Access Journals (Sweden)

J. Williams

2011-11-01

Full Text Available Nighttime mixing ratios of boundary layer N2O5 were determined using cavity-ring-down spectroscopy during the DOMINO campaign in Southern Spain (Diel Oxidant Mechanisms In relation to Nitrogen Oxides, 21 November 2008–8 December 2008. N2O5 mixing ratios ranged from below the detection limit (~5 ppt to ~500 ppt. A steady-state analysis constrained by measured mixing ratios of N2O5, NO2 and O3 was used to derive NO3 lifetimes and compare them to calculated rates of loss via gas-phase and heterogeneous reactions of both NO3 and N2O5. Three distinct types of air masses were encountered, which were largely marine (Atlantic, continental or urban-industrial in origin. NO3 lifetimes were longest in the Atlantic sector (up to ~30 min but were very short (a few seconds in polluted, air masses from the local city and petroleum-related industrial complex of Huelva. Air from the continental sector was an intermediate case. The high reactivity to NO3 of the urban air mass was not accounted for by gas-phase and heterogeneous reactions, rates of which were constrained by measurements of NO, volatile organic species and aerosol surface area. In general, high NO2 mixing ratios were associated with low NO3 lifetimes, though heterogeneous processes (e.g. reaction of N2O5 on aerosol were generally less important than direct gas-phase losses of NO3. The presence of SO2 at levels above ~2 ppb in the urban air sector was always associated with very low N2O5 mixing ratios indicating either very short NO3 lifetimes in the presence of combustion-related emissions or an important role for reduced sulphur species in urban, nighttime chemistry. High production rates coupled with low lifetimes of NO3 imply an important contribution of nighttime chemistry to removal of both NOx and VOC.

Rational design and synthesis of Ni x Co 3−x O 4 nanoparticles derived from multivariate MOF-74 for supercapacitors

KAUST Repository

Chen, Siru

2015-01-01

© The Royal Society of Chemistry 2015. Mixed transition metal oxides have attracted much attention recently due to their potential application in energy and environmental sciences. The emergence of multivariate MOFs recently has attracted great research attention and provides an opportunity for multivariate mixed-metal oxides. In this work, five isostructural, single-phase MOF-74 structures with different divalent metals (MOF-74-Co, MOF-74-Ni, MOF-74-NiCo1, MOF-74-NiCo2 and MOF-74-NiCo4) were synthesised by varying the mole ratios of Ni/Co mixed-metal ions. After annealing at the appropriate temperature, Co3O4, NiO and three kinds of NixCo3-xO4 mixed-metal oxide nanoparticles with high surface area were easily obtained and the metal ratio was readily controlled, enabling us to systematically investigate the effect of different metal species amounts on the electrochemical properties of the mixed-metal oxide materials. When these metal oxides were used as electrode materials for supercapacitors, we found that the mixed-metal oxides NixCo3-xO4 obtained from bimetallic MOF-74-NiCo structures had obvious advantages compared with the monometallic oxides of MOF-74-Ni and MOF-74-Co. In particular, the NixCo3-xO4-1 with the Ni/Co metal ratio 1:1 exhibited the highest capacitance of 797 F g-1 and excellent cycling stability.

The Impact of Volute Aspect Ratio on the Performance of a Mixed Flow Turbine

Directory of Open Access Journals (Sweden)

Samuel P. Lee

2017-11-01

Full Text Available Current trends in the automotive industry towards engine downsizing mean turbocharging now plays a vital role in engine performance. A turbocharger increases charge air density using a turbine to extract waste energy from the exhaust gas to drive a compressor. Most turbocharger applications employ a radial inflow turbine. However, mixed flow turbines can offer non-zero blade angles, reducing leading edge (LE separation at low velocity ratios. The current paper investigates the performance of a mixed flow turbine with three different volute aspect ratio (AR designs (AR = 0.5, 1 and 2. With constant A/r (ratio of volute area to centroid radius, the AR = 0.5 volute design produced a 4.3% increase in cycle averaged mass flow parameter (MFP compared to the AR = 2 design. For the purpose of performance comparison, it was necessary to manipulate the volute A/r’s to ensure constant MFP for aerodynamic similarity. With the volute A/r’s manipulated to ensure constant MFP for aerodynamic similarity, the maximum variation of cycle averaged normalized efficiency measured between the designs was 1.47%. Purely in the rotor region, the variation in normalized cycle averaged efficiency was 1%. The smallest tested volute aspect ratio showed a significant increase in volute loss while the ARs of 1 and 2 showed similar levels of loss. The smallest AR volute showed significant secondary flow development in the volute. The resulting variation in LE incidence was found to vary as a result.

Multipole mixing ratios in /sup 154/Gd

Energy Technology Data Exchange (ETDEWEB)

Chung, Won Mo; Song, Choong Sik; Joo, Koan Sik

1985-06-01

We have measured gamma-gamma angular correlations to determine the mixing ratios of several gamma transitions in /sup 154/Gd. The results are compared with those derived from the pairing-plus-quadrupole model and from the interacting boson model.

The effect of Cu/Zn molar ratio on CO{sub 2} hydrogenation over Cu/ZnO/ZrO{sub 2}/Al{sub 2}O{sub 3} catalyst

Energy Technology Data Exchange (ETDEWEB)

Shaharun, Salina, E-mail: salinashaharun@gmail.com, E-mail: maizats@petronas.com.my; Shaharun, Maizatul S., E-mail: salinashaharun@gmail.com, E-mail: maizats@petronas.com.my; Taha, Mohd F., E-mail: faisalt@petronas.com.my [Department of Fundamental and Applied Science, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 31750 Tronoh, Perak (Malaysia); Mohamad, Dasmawati, E-mail: dasmawati@kck.usm.my [School of Dental Sciences, Health Campus, Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan (Malaysia)

2014-10-24

Catalytic hydrogenation of carbon dioxide (CO{sub 2}) to methanol is an attractive way to recycle and utilize CO{sub 2}. A series of Cu/ZnO/Al{sub 2}O{sub 3}/ZrO{sub 2} catalysts (CZAZ) containing different molar ratios of Cu/Zn were prepared by the co-precipitation method and investigated in a stirred slurry autoclave system. The catalysts were characterized by temperature-programmed reduction (TPR), field emission scanning electron microscopy-energy dispersive analysis (FESEM-EDX), X-ray diffraction (XRD) and N{sub 2} adsorption-desorption. Higher surface area, SA{sub BET} values (42.6–59.9 m{sup 2}/g) are recorded at low (1) and high (5) Cu/Zn ratios with the minimum value of 35.71 m{sup 2}/g found for a Cu/Zn of 3. The reducibility of the metal oxides formed after calcination of catalyst samples was also affected due to change in metal-support interaction. At a low reaction temperature of 443 K, total gas pressure of 3.0 MPa and 0.1 g/mL of the CZAZ catalyst, the selectivity to methanol decreased as the Cu/Zn molar ratio increased, and the maximum selectivity of 67.73 was achieved at Cu/Zn molar ratio of 1. With a reaction time of 3h, the best performing catalyst was CZAZ75 with Cu/Zn molar ratio of 5 giving methanol yield of 79.30%.

On the cross-sensitivity between water vapor mixing ratio and stable isotope measurements of in-situ analyzers

KAUST Repository

Parkes, Stephen

2015-04-01

In recent years there has been an increasing amount of water vapor stable isotope data collected using in-situ instrumentation. A number of papers have characterized the performance of these in-situ analyzers and suggested methods for calibrating raw measurements. The cross-sensitivity of the isotopic measurements on the mixing ratio has been shown to be a major uncertainty and a variety of techniques have been suggested to characterize this inaccuracy. However, most of these are based on relating isotopic ratios to water vapor mixing ratios from in-situ analyzers when the mixing ratio is varied and the isotopic composition kept constant. An additional correction for the span of the isotopic ratio scale is then applied by measuring different isotopic standards. Here we argue that the water vapor cross-sensitivity arises from different instrument responses (span and offset) of the parent H2O isotope and the heavier isotopes, rather than spectral overlap that could cause a true variation in the isotopic ratio with mixing ratio. This is especially relevant for commercial laser optical instruments where absorption lines are well resolved. Thus, the cross-sensitivity determined using more conventional techniques is dependent on the isotopic ratio of the standard used for the characterization, although errors are expected to be small. Consequently, the cross-sensitivity should be determined by characterizing the span and zero offset of each isotope mixing ratio. In fact, this technique makes the span correction for the isotopic ratio redundant. In this work we model the impact of changes in the span and offset of the heavy and light isotopes and illustrate the impact on the cross-sensitivity of the isotopic ratios on water vapor. This clearly shows the importance of determining the zero offset for the two isotopes. The cross-sensitivity of the isotopic ratios on water vapor is then characterized by determining the instrument response for the individual isotopes for a

On the cross-sensitivity between water vapor mixing ratio and stable isotope measurements of in-situ analyzers

KAUST Repository

Parkes, Stephen; Wang,  Lixin; McCabe, Matthew

2015-01-01

In recent years there has been an increasing amount of water vapor stable isotope data collected using in-situ instrumentation. A number of papers have characterized the performance of these in-situ analyzers and suggested methods for calibrating raw measurements. The cross-sensitivity of the isotopic measurements on the mixing ratio has been shown to be a major uncertainty and a variety of techniques have been suggested to characterize this inaccuracy. However, most of these are based on relating isotopic ratios to water vapor mixing ratios from in-situ analyzers when the mixing ratio is varied and the isotopic composition kept constant. An additional correction for the span of the isotopic ratio scale is then applied by measuring different isotopic standards. Here we argue that the water vapor cross-sensitivity arises from different instrument responses (span and offset) of the parent H2O isotope and the heavier isotopes, rather than spectral overlap that could cause a true variation in the isotopic ratio with mixing ratio. This is especially relevant for commercial laser optical instruments where absorption lines are well resolved. Thus, the cross-sensitivity determined using more conventional techniques is dependent on the isotopic ratio of the standard used for the characterization, although errors are expected to be small. Consequently, the cross-sensitivity should be determined by characterizing the span and zero offset of each isotope mixing ratio. In fact, this technique makes the span correction for the isotopic ratio redundant. In this work we model the impact of changes in the span and offset of the heavy and light isotopes and illustrate the impact on the cross-sensitivity of the isotopic ratios on water vapor. This clearly shows the importance of determining the zero offset for the two isotopes. The cross-sensitivity of the isotopic ratios on water vapor is then characterized by determining the instrument response for the individual isotopes for a

Mixed-Alkali Effect in Li2O-Na2O-K2O-B2O3 Glasses: Infrared and Optical Absorption Studies

Science.gov (United States)

Samee, M. A.; Edukondalu, A.; Ahmmad, Shaik Kareem; Taqiullah, Sair Md.; Rahman, Syed

2013-08-01

The mixed-alkali effect (MAE) has been investigated in the glass system (40 - x)Li2O- xNa2O-10K2O-50B2O3 (0 mol% ≤ x ≤ 40 mol%) through density, modulated differential scanning calorimetry (DSC), and optical absorption studies. From the absorption studies, the values of the optical band gap ( E opt) for direct transition and Urbach energy (Δ E) have been evaluated. The values of E opt and Δ E show nonlinear behavior with the compositional parameter. The density and glass-transition temperature of the present glasses also show nonlinear variation, supporting the existence of MAE. The infrared (IR) spectra of the glasses reveal the presence of three- and four-coordinated boron atoms. The specific vibrations of Li-O, Na-O, and K-O bonds were observed in the present IR study.

Aircraft observations of aerosols O3 and NOy in a nighttime urban plume

International Nuclear Information System (INIS)

Berkowitz, C.M.; Zaveri, R.A.; Xindi Bian; Shiyuan Zhong; Disselkamp, R.S.; Laulainen, N.S.; Chapman, E.G.

2001-01-01

Nighttime measurements of aerosol surface area, O 3 , NO y and moisture were made downwind of Portland, Oregon, as part of a study to characterize the chemistry in a nocturnal urban plume. Air parcels sampled within the urban plume soon after sunset had positive correlations between O 3 , relative humidity, NO y and aerosol number density. However, the air parcels sampled within the urban plume just before dawn had O 3 mixing ratios that were highly anti-correlated with aerosol number density, NO y and relative humidity. Back-trajectories from a mesoscale model show that both the post-sunset and pre-dawn parcels came from a common maritime source to the northwest of Portland. The pre-dawn parcels with strong anti-correlations passed directly over Portland in contrast to the other parcels that were found to pass west of Portland. Several gas-phase mechanisms and a heterogeneous mechanism involving the loss of O 3 to the aerosol surface, are examined to explain the observed depletion in O 3 within the pre-dawn parcels that had passed over Portland. (Author)

Ce-Fe-O mixed oxide as oxygen carrier for the direct partial oxidation of methane to syngas

Institute of Scientific and Technical Information of China (English)

魏永刚; 王华; 李孔斋

2010-01-01

The Ce-Fe-O mixed oxide with a ratio of Ce/Fe=7:3, which was prepared by coprecipitation method and employed as oxygen carrier, for direct partial oxidation of methane to syngas in the absence of gaseous oxygen was explored. The mixed oxide was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM), and the catalytic performances were studied in a fixed-bed quartz reactor and a thermogravimetric reactor, respectively. Approximately 99.4% H2 se...

A sublimation technique for high-precision measurements of δ13CO2 and mixing ratios of CO2 and N2O from air trapped in ice cores

Directory of Open Access Journals (Sweden)

H. Fischer

2011-07-01

Full Text Available In order to provide high precision stable carbon isotope ratios (δ13CO2 or δ13C of CO2 from small bubbly, partially and fully clathrated ice core samples we developed a new method based on sublimation coupled to gas chromatography-isotope ratio mass spectrometry (GC-IRMS. In a first step the trapped air is quantitatively released from ~30 g of ice and CO2 together with N2O are separated from the bulk air components and stored in a miniature glass tube. In an off-line step, the extracted sample is introduced into a helium carrier flow using a minimised tube cracker device. Prior to measurement, N2O and organic sample contaminants are gas chromatographically separated from CO2. Pulses of a CO2/N2O mixture are admitted to the tube cracker and follow the path of the sample through the system. This allows an identical treatment and comparison of sample and standard peaks. The ability of the method to reproduce δ13C from bubble and clathrate ice is verified on different ice cores. We achieve reproducibilities for bubble ice between 0.05 ‰ and 0.07 ‰ and for clathrate ice between 0.05 ‰ and 0.09 ‰ (dependent on the ice core used. A comparison of our data with measurements on bubble ice from the same ice core but using a mechanical extraction device shows no significant systematic offset. In addition to δ13C, the CO2 and N2O mixing ratios can be volumetrically derived with a precision of 2 ppmv and 8 ppbv, respectively.

Effect of plant density and mixing ratio on crop yield in sweet corn/mungbean intercropping.

Science.gov (United States)

Sarlak, S; Aghaalikhani, M; Zand, B

2008-09-01

In order to evaluate the ear and forage yield of sweet corn (Zea mays L. var. Saccarata) in pure stand and intercropped with mung bean (Vigna radiata L.), a field experiment was conducted at Varamin region on summer 2006. Experiment was carried out in a split plot design based on randomized complete blocks with 4 replications. Plant density with 3 levels [Low (D1), Mean (D2) and High (D3) respecting 6, 8 and 10 m(-2) for sweet corn, cultivar S.C.403 and 10, 20 and 30 m(-2) for mung bean cultivar, Partow] was arranged in main plots and 5 mixing ratios [(P1) = 0/100, (P2) = 25/75, (P3) = 50/50, (P4) = 75/25, (P5) = 100/0% for sweet corn/mung bean, respectively] were arranged in subplots. Quantitative attributes such as plant height, sucker numbers, LER, dry matter distribution in different plant organs were measured in sweet corn economical maturity. Furthermore the yield of cannable ear corn and yield components of sweet corn and mung bean were investigated. Results showed that plant density has not any significant effect on evaluated traits, while the effect of mixing ratio was significant (p ratio of 75/25 (sweet corn/mung bean) could be introduced as the superior mixing ratio; because of it's maximum rate of total sweet corn's biomass, forage yield, yield and yield components of ear corn in intercropping. Regarding to profitability indices of intercropping, the mixing ratio 75/25 (sweet corn/mung bean) in low density (D1P2) which showed the LER = 1.03 and 1.09 for total crop yield before ear harvesting and total forage yield after ear harvest respectively, was better than corn or mung bean monoculture.

4,6-Dimethyl-dibenzothiophene conversion over Al{sub 2}O{sub 3}-TiO{sub 2}-supported noble metal catalysts

Energy Technology Data Exchange (ETDEWEB)

Nunez, Sara [Departamento de Ingenieria de Procesos e Hidraulica, Universidad Autonoma Metropolitana-Iztapalapa, San Rafael Atlixco 186, Vicentina, Iztapalapa, 09340, Mexico, D.F. (Mexico); Escobar, Jose, E-mail: jeaguila@imp.mx [Instituto Mexicano del Petroleo, Eje Central Lazaro Cardenas 152, San Bartolo Atepehuacan, Gustavo A. Madero, 07730, Mexico, D.F. (Mexico); Vazquez, Armando; Reyes, Jose Antonio de los [Departamento de Ingenieria de Procesos e Hidraulica, Universidad Autonoma Metropolitana-Iztapalapa, San Rafael Atlixco 186, Vicentina, Iztapalapa, 09340, Mexico, D.F. (Mexico); Hernandez-Barrera, Melissa [Instituto Mexicano del Petroleo, Eje Central Lazaro Cardenas 152, San Bartolo Atepehuacan, Gustavo A. Madero, 07730, Mexico, D.F. (Mexico)

2011-03-15

Research highlights: {yields} Al{sub 2}O{sub 3} and Al{sub 2}O{sub 3}-TiO{sub 2} (molar ratio Al/Ti = 2, AT2) mixed oxides were pore-filling impregnated to obtain Pd, Pt and Pd-Pt catalysts with {approx}1 wt% nominal metal loading. {yields} Reduced catalysts were tested in the 4,6-dimethyl-dibenzothiophene hydrodesulfurization (HDS). {yields} In Pd-containing materials, TiO{sub 2} incorporation into the alumina support was favorable to the catalytic activity of noble metal catalysts. {yields} Enhanced intrinsic activity (per exposed metallic site) was obtained in Pt-containing catalysts supported on the AT2 mixed oxide. {yields} Yield to different products over various catalysts seemed to be strongly influenced by metallic particles dispersion. - Abstract: Al{sub 2}O{sub 3} and Al{sub 2}O{sub 3}-TiO{sub 2} (molar ratio Al/Ti = 2, AT2) mixed oxides were synthesized using a low-temperature sol-gel method and were further pore-filling impregnated to obtain Pd and Pt catalysts with {approx}1 wt% nominal metal loading. Simultaneous impregnation was used to prepare bimetallic materials at Pd:Pt = 80:20. Solids characterization was carried out by N{sub 2}-physisorption, high-resolution transmission electron microscopy (HR-TEM and E-FTEM), X-ray diffraction, temperature-programmed reduction and CO-chemisorption. Reduced (350 deg. C, H{sub 2} flow) catalysts were tested in the 4,6-dimethyl-dibenzothiophene hydrodesulfurization (HDS) (in n-dodecane, at 300 deg. C and 5.5 MPa, batch reactor). In Pd-containing materials, TiO{sub 2} incorporation into the alumina support was favorable to the catalytic activity of noble metal catalysts, where bimetallic Pd-Pt with AT2 carrier had the highest organo-S compound conversion. Enhanced intrinsic activity (per exposed metallic site) was obtained in Pt-containing catalysts supported on the AT2 mixed oxide (as compared to alumina-supported ones). Yield to different products over various catalysts seemed to be strongly influenced by

The effect of B{sub 2}O{sub 3} flux on growth NLBCO superconductor by solid state reaction and wet-mixing methods

Energy Technology Data Exchange (ETDEWEB)

Suharta, W. G., E-mail: wgsuharta@gmail.com; Wendri, N.; Ratini, N.; Suarbawa, K. N. [Departement of Physics Faculty of Mathematics and Natural Science Udayana University Bali Indonesia (Indonesia)

2016-03-11

The synthesis of B{sub 2}O{sub 3} flux substituted NLBCO superconductor NdBa{sub 1.75}La{sub 0.25}Cu{sub 3}O{sub 7-∂} has been done using solid state reaction and wet-mixing methods in order to obtain homogeneous crystals and single phase. From DTA/TGA characteritations showed the synthesis process by wet-mixing requires a lower temperature than the solid state reaction in growing the superconductor NdBa{sub 1.75}La{sub 0.25}Cu{sub 3}O{sub 7-∂}. Therefore, in this research NdBa{sub 1.75}La{sub 0.25}Cu{sub 3}O{sub 7-∂} sample calcinated at 650°C for wet-mixing method and 820°C for solid state reaction methods. The all samples was sintered at 950°C for ten hours. Crystallinity of the sample was confirmed using X-ray techniques and generally obtained sharp peaks that indicates the sample already well crystallized. Search match analyses for diffraction data gave weight fractions of impurity phase of the solid state reaction method higher than wet-mixing method. In this research showed decreasing the price of the lattice parameter about 1% with the addition of B{sub 2}O{sub 3} flux for the both synthesis process and 2% of wet mixing process for all samples. Characterization using scanning electron microscopy (SEM) showed the distribution of crystal zise for wet-mixing method more homogeneous than solid state reaction method, with he grain size of samples is around 150–250 nm. The results of vibrating sample magnetometer (VSM) showed the paramagnetic properties for all samples.

Volatile organic compound mixing ratios above Beijing in November and December 2016

Science.gov (United States)

Acton, William; Shaw, Marvin; Huang, Zhonghui; Wang, Zhaoyi; Wang, Xinming; Zhang, Yanli; Davison, Brian; Langford, Ben; Mullinger, Neil; Nemitz, Eiko; Fu, Pingqing; Squires, Freya; Carpenter, Lucy; Lewis, Alastair; Hewitt, Nick

2017-04-01

Volatile organic compounds (VOCs) are emitted into the atmosphere from vegetation and anthropogenic sources such as fossil fuel combustion, biomass burning and the evaporation of petroleum products. These compounds play an important role in the chemistry of the lower atmosphere through secondary organic aerosol (SOA) formation and facilitating the formation of tropospheric ozone. As well as their indirect impact on human health via the formation of ozone and SOA, some VOCs, including benzene, directly affect human health adversely. Here we report VOC mixing ratios measured in Beijing during a 5 week intensive field campaign from the 7th November to the 10th December 2016. This work was carried out as part of the Sources and Emissions of Air Pollutants in Beijing (AIRPOLL-Beijing) work project within the Air Pollution and Human Health in a Developing Megacity (APHH-Beijing) research programme. APHH is a large multi-institutional study which aims to record the concentrations and identify the sources of urban air pollutants in Beijing, determine exposure, understand their effects on human health, and to identify solutions. VOC mixing ratios were recorded using a Proton Transfer Reaction-Time of Flight-Mass Spectrometer (PTR-ToF-MS, Ionicon Analytik) and a Selected Ion Flow Tube-Mass Spectrometer (SIFT-MS, SYFT Technologies). During the measurement period Beijing was subject to multiple pollution events that alternated with periods of relatively good air quality, allowing the VOCs within the polluted air masses to be identified and quantified. VOCs were sampled at 102 m with additional gradient measurements made at 3, 15, 32 and 64 m providing a vertical profile of VOC mixing ratios. Mixing ratios of methanol, acetonitrile, acetaldehyde, acetone, isoprene and aromatics species will be reported together with a discussion of potential sources. Comparisons will then be drawn with other large cities.

NH3/O2 mixed gas plasmas alter the interaction of blood components with stainless steel.

Science.gov (United States)

Chen, Meng; Zamora, Paul O; Peña, Louis; Som, Prantika; Osaki, Shigemasa

2003-12-01

Stainless steel treated with a mixed gas plasma of NH(3) plus O(2) had chemical and biologic characteristics distinct from untreated stainless steel or stainless steel treated with NH(3) or O(2) plasmas used separately. NH(3)/O(2) plasmas deposited nitrogen as both -CN (organic) and -NO (nitrate, nitrite)--materials not found on untreated stainless steel--and the contact angle changed from 44 degrees to 23 degrees. Treatment of stainless steel (and titanium) resulted in surfaces with enhanced resistance to platelet and leukocyte attachment. A gas plasma of N(2)O/O(2) also was found to reduce platelet and leukocyte attachment, suggesting that these properties may be common to surfaces coated with oxynitrites (nitrides). Upon subcutaneous implantation, no inflammation, hemolysis, or untoward thrombosis was noted in the tissue surrounding the wafers treated with the NH(3)/O(2) plasmas, although the cellular density was considerably reduced by 2 weeks after implant. Collectively, the results suggest that NH(3)/O(2) plasmas impart a unique character to stainless steel that may be useful in the construction of medical devices. Copyright 2003 Wiley Periodicals, Inc. J Biomed Mater Res 67A: 994-1000, 2003

Synthesis of nanostructured mixed oxide CeO2-Mn2O3 and investigation of their sorption ability for arsenic, ammoniac, iron, manganese

International Nuclear Information System (INIS)

Luu Minh Dai; Dao Ngoc Nhiem; Duong Thi Lim

2012-01-01

The nanostrutured mixed oxide CeO 2 -Mn 2 O 3 have been synthesised at low temperature (350 o C) by the combustion of gel prepared from polyvinyl alcohol (PVA), Ce (NO 3 ) 4 and Mn(No 3 ) 3 , CeO 2 -Mn 2 O 3 characterizations were examined by X-ray diffraction (XRD), scanning electron microscopy (SEM) and BET (Brunauce-Emmet-Teller) measurements. The phase of CeO 2 -Mn 2 O 3 , with large specific surface ares 65.3 m 2 /g was obtained at 350 o C for 2 hours. The nanostructured CeO 2 -Mn 2 O 3 has been investigated for removing iron, manganese, arsenic and ammoniac from water. The sorption characteristics of the nanostrutured CeO 2 -Mn 2 O 3 for AS(V), NH4 + , Fe(III), Mn(II) according to the langmuir isotherm. The sorption capacities of nanostrutured CeO 2 -Mn 2 O 3 are 57.10 mg As(V)g; 154.54 mg NH4 + /g; 72.97 mg Fe(III)/g; 60.27 Mn(II) / g. (author)

Preparation and Study of NH3 Gas Sensing Behavior of Fe2O3 Doped ZnO Thick Film Resistors

Directory of Open Access Journals (Sweden)

D. R. Patil

2006-08-01

Full Text Available The preparation, characterization and gas sensing properties of pure and Fe2O3-ZnO mixed oxide semiconductors have been investigated. The mixed oxides were obtained by mixing ZnO and Fe2O3 in the proportion 1:1, 1:0.5 and 0.5:1. Pure ZnO was observed to be insensitive to NH3 gas. However, mixed oxides (with ZnO: Fe2O3 =1:0.5 were observed to be highly sensitive to ammonia gas. Upon exposure to NH3 gas, the barrier height of Fe2O3-ZnO intergranular regions decreases markedly due to the chemical transformation of Fe2O3 into well conducting ferric ammonium hydroxide leading to a drastic decrease in resistance. The crucial gas response was found to NH3 gas at 3500C and no cross response was observed to other hazardous and polluting gases. The effects of microstructure and doping concentration on the gas response, selectivity, response and recovery of the sensor in the presence of NH3 gas were studied and discussed.

Synthesis of mixed-valent {alpha}- and {beta}-NaFe{sub 2}O{sub 3} polymorphs under controlled partial oxygen pressure

Energy Technology Data Exchange (ETDEWEB)

Bruno, Shaun R.; Blakely, Colin K. [Department of Chemistry, Michigan State University, East Lansing, MI 48824 (United States); Poltavets, Viktor V., E-mail: poltavets@chemistry.msu.edu [Department of Chemistry, Michigan State University, East Lansing, MI 48824 (United States)

2012-08-15

Synthesis of mixed valent compounds, especially when multiple polymorphs exist, requires careful control of the preparation conditions. {alpha}- and {beta}-NaFe{sub 2}O{sub 3} polymorphs were synthesized under controlled partial oxygen pressure (pO{sub 2}). pO{sub 2} regions of stability at 850 Degree-Sign C were determined for both phases for the first time. A modified oxygen buffer method was developed for the facile preparation of mixed valent oxides under controlled pO{sub 2}. {beta}-NaFe{sub 2}O{sub 3} is the only known n=2 member of the AM{sub n}O{sub n+1} (A=alkali metal, M=3d metal) rock-salt related homolog series with layered cation ordering. The possibility of new members of the homolog series with other 3d metals is considered. - Graphical abstract: Schematic section of phase composition vs. partial O{sub 2} pressure diagram at 850 Degree-Sign C for Na/Fe=1/2 and structure models of {alpha}- and {beta}-NaFe{sub 2}O{sub 3}. Highlights: Black-Right-Pointing-Pointer {alpha}- and {beta}-NaFe{sub 2}O{sub 3} polymorphs were synthesized under controlled oxygen pressure. Black-Right-Pointing-Pointer {beta}-NaFe{sub 2}O{sub 3} has rock-salt related structure with layered cation ordering. Black-Right-Pointing-Pointer Existence of the rock-salt related homolog series AM{sub n}O{sub n+1} is discussed.

Mixing up-conversion excitation behaviors in Er3+/Yb3+-codoped aluminum germanate glasses for visible waveguide devices

International Nuclear Information System (INIS)

Gong, H.; Lin, L.; Zhao, X.; Pun, E.Y.B.; Yang, D.L.; Lin, H.

2010-01-01

A mixing up-conversion excitation phenomenon in Er 3+ /Yb 3+ -codoped aluminum germanate (Na 2 O-MgO-Al 2 O 3 -GeO 2 , NMAG for short) glasses for K + -Na + ion-exchanged waveguides was observed and characterized. The green and red up-conversion luminescence of Er 3+ is due to a two-photon excitation process under low-power excitation of a 974 nm diode laser, however, with increasing the pumping power, the green emission turns to follow a combination of two- and three-photon excitation effects while the red one still agrees with a two-photon excitation law. Under high-power pumping, owing to potential thermal effect, the population ratio between the 2 H 11/2 and 4 S 3/2 levels adjusts acutely, which results in a distinct exhibition in 2 H 11/2 → 4 I 15/2 and 4 S 3/2 → 4 I 15/2 emission transitions. Green transmission trace has been observed in K + -Na + ion-exchanged Er 3+ /Yb 3+ -codoped NMAG glass waveguide and it provides an original reference in developing visible waveguide amplifiers and lasers.

A chiral mixed carboxylate, [Nd4(H2O)2(OOC(CH2)3COO)4(C2O4)2], exhibiting NLO properties

International Nuclear Information System (INIS)

Vaidhyanathan, R.; Natarajan, Srinivasan; Rao, C.N.R.

2004-01-01

Reaction of a mixture of neodymium carbonate, HCl, oxamic acid and glutaric acid under hydrothermal conditions gives rise to a new mixed carboxylate of neodymium, [Nd 4 (H 2 O) 2 (OOC(CH 2 ) 3 COO) 4 (C 2 O 4 ) 2 ], I. The structure, determined using single crystal X-ray diffraction, comprises a helical column formed by the grafting of the oxalate unit on to helical NdO 9 chains, cross-linked by the glutarate anions. It is noteworthy that the pitch of the helix is equivalent to the length of the oxalate unit. Furthermore, I shows about 1.1 times the SHG activity of urea

Mixing-induced groundwater denitrification beneath a manured field in southern Alberta, Canada

International Nuclear Information System (INIS)

McCallum, J.E.; Ryan, M.C.; Mayer, B.; Rodvang, S.J.

2008-01-01

Contamination of shallow groundwater by NO 3 - from manure may occur under fields where manure is spread as fertilizer and for disposal. Attenuation of NO 3 - in groundwater occurs through denitrification under certain conditions, or NO 3 - -contaminated younger groundwater may mix with older groundwater, lowering the NO 3 - concentration. In this study, δ 15 N and δ 18 O values of NO 3 - , and δ 18 O and δ 2 H values in groundwater under a manured field were evaluated to determine if groundwater NO 3 - concentrations were influenced through mixing of shallower, manure-impacted groundwater with older groundwater, or if denitrification was reducing NO 3 - concentrations. The younger groundwater showed clear evidence of manure impact with elevated Cl - (∼85 mg L -1 ) and NO 3 - concentrations (∼50 mg NO 3 -N L -1 ), and δ 15 N and δ 18 O values of NO 3 - consistent with a manure source. Vertical hydraulic gradients and δ 18 O and δ 2 H values in groundwater suggest older, more reduced groundwater is upwelling locally and mixing with the shallow groundwater. Decreasing NO 3 :Cl ratios, decreasing dissolved O 2 concentrations, and increasing δ 15 N and δ 18 O values of NO 3 - suggest that denitrification occurs locally in the aquifer. The extent of denitrification is proportional to the fraction of deeper groundwater in the aquifer. Denitrification apparently does not proceed in the younger, manure-impacted groundwater in the absence of mixing

Ion sensing properties of vanadium/tungsten mixed oxides

International Nuclear Information System (INIS)

Guidelli, Eder Jose; Guerra, Elidia Maria; Mulato, Marcelo

2011-01-01

Vanadium/tungsten mixed oxide (V 2 O 5 /WO 3 ) sensing membranes were deposited on glassy carbon substrates and used as the H + sensor of the extended gate field effect transistor (EGFET) device. X-ray diffractograms indicated a decrease of the interplanar spacing of V 2 O 5 after the insertion of WO 3 revealing that the lamellar structure is under compressive stress. The crystallinity increases with increasing WO 3 molar ratio. The film is not homogeneous, with more WO 3 material sitting at the surface. This influences the response of pH sensors using the EGFET configuration. The maximum sensitivity of 68 mV pH -1 was obtained for the sample with 5% WO 3 molar ratio. For higher WO 3 molar ratios, the behavior is not linear. It can be concluded that V 2 O 5 dominates for acidic solutions while WO 3 dominates for basic solutions. Therefore, the mixed oxide with low amount of WO 3 is the main candidate for further use as biosensor.

Contrasting winter and summer VOC mixing ratios at a forest site in the Western Mediterranean Basin: the effect of local biogenic emissions

Science.gov (United States)

Seco, R.; Peñuelas, J.; Filella, I.; Llusià, J.; Molowny-Horas, R.; Schallhart, S.; Metzger, A.; Müller, M.; Hansel, A.

2011-12-01

Atmospheric volatile organic compounds (VOCs) are involved in ozone and aerosol generation, thus having implications for air quality and climate. VOCs and their emissions by vegetation also have important ecological roles as they can protect plants from stresses and act as communication cues between plants and between plants and animals. In spite of these key environmental and biological roles, the reports on seasonal and daily VOC mixing ratios in the literature for Mediterranean natural environments are scarce. We conducted seasonal (winter and summer) measurements of VOC mixing ratios in an elevated (720 m a.s.l.) holm oak Mediterranean forest site near the metropolitan area of Barcelona (NE Iberian Peninsula). Methanol was the most abundant compound among all the VOCs measured in both seasons. While aromatic VOCs showed almost no seasonal variability, short-chain oxygenated VOCs presented higher mixing ratios in summer, presumably due to greater emission by vegetation and increased photochemistry, both enhanced by the high temperatures and solar radiation in summer. Isoprenoid VOCs showed the biggest seasonal change in mixing ratios: they increased by one order of magnitude in summer, as a result of the vegetation's greater physiological activity and emission rates. The maximum diurnal concentrations of ozone increased in summer too, most likely due to more intense photochemical activity and the higher levels of VOCs in the air. The daily variation of VOC mixing ratios was mainly governed by the wind regime of the mountain, as the majority of the VOC species analyzed followed a very similar diel cycle. Mountain and sea breezes that develop after sunrise advect polluted air masses to the mountain. These polluted air masses had previously passed over the urban and industrial areas surrounding the Barcelona metropolitan area, where they were enriched in NOx and in VOCs of biotic and abiotic origin. Moreover, these polluted air masses receive additional biogenic

Sensing Properties of Pd-Loaded Co3O4 Film for a ppb-Level NO Gas Sensor

Directory of Open Access Journals (Sweden)

Takafumi Akamatsu

2015-04-01

Full Text Available We prepared 0.1 wt%–30 wt% Pd-loaded Co3O4 by a colloidal mixing method and investigated the sensing properties of a Pd-loaded Co3O4 sensor element, such as the sensor response, 90% response time, 90% recovery time, and signal-to-noise (S/N ratio, toward low nitric oxide (NO gas levels in the range from 50 to 200 parts per billion. The structural properties of the Pd-loaded Co3O4 powder were investigated using X-ray diffraction analysis and transmission electron microscopy. Pd in the powder existed as PdO. The sensor elements with 0.1 wt%–10 wt% Pd content have higher sensor properties than those without any Pd content. The response of the sensor element with a 30 wt% Pd content decreased markedly because of the aggregation and poor dispersibility of the PdO particles. High sensor response and S/N ratio toward the NO gas were achieved when a sensor element with 10 wt% Pd content was used.

Characterisation and Properties of Lithium Disilicate Glass Ceramics in the SiO2-Li2O-K2O-Al2O3 System for Dental Applications

Directory of Open Access Journals (Sweden)

Naruporn Monmaturapoj

2013-01-01

Full Text Available This work proposes four different glass formulas derived from the SiO2-Li2O-K2O-Al2O3 system to investigate the effect of glass composition on their crystal formations and properties. Glass LD1 was SiO2-Li2O-K2O-Al2O3 system with the addition of P2O5 and CaF2 as nucleating agents. In Glass LD2, a slight amount of MgO was mixed in order to increase the viscosity of the melting glass. Finally, the important factor of Si : Li ratio was increased in Glasses LD3 and LD4 with compositions otherwise the same as LD1 and LD2. The results found that P2O5 and CaF2 served as a nucleating site for lithium phosphate and fluorapatite to encourage heterogenous nucleation and produce a fine-grained interlocking microstructure of lithium disilicate glass ceramics. MgO content in this system seemed to increase the viscosity of the melting glass and thermal expansion coefficient including the chemical solubility. Increasing the Si : Li ratio in glass compositions resulted in the change of the microstructure of Li2Si2O5 crystals.

Improved performance of solution-processed a-InGaZnO thin-film transistors due to Ar/O{sub 2} mixed-plasma treatment

Energy Technology Data Exchange (ETDEWEB)

Kim, Kwan-Soo; Hwang, Yeong-Hyeon; Hwang, In-Chan; Cho, Won-Ju [Kwangwoon University, Seoul (Korea, Republic of)

2014-08-15

We investigated the effects of Ar and O{sub 2} treatment and of Ar/O{sub 2} mixed plasma treatment on the electrical characteristics of solution-processed amorphous indium-gallium-zinc-oxide (a-IGZO) thin-film transistors (TFTs). The electrical performance and the instability of a-IGZO TFTs were significantly improved by the plasma treatments. The plasma treatments reduced the carbon-based residual contamination that acted as possible trap sites. In particular, the O{sub 2}-plasma treatment produced a significant improvement in the reliability of a-IGZO TFTs when compared with the Ar-plasma-treated device, owing to the elimination of residual carbon in the active channel of the solution-processed a-IGZO. However, the optimized improvement of the solution-processed a-IGZO TFT under a gate bias stress was obtained for the device treated with an Ar/O{sub 2} mixed-gas plasma. The plasma treatment in the Ar/O{sub 2}-mixed ambience remarkably enhanced not only the reliability but also the electrical performance of the a-IGZO TFT; the on/off-current ratio, the field-effect mobility, and the subthreshold slope were 6.78 x 10{sup 7}, 1.24 cm{sup 2}/V·s, and 513 mV/dec, respectively.

Trial synthesis of Li{sub 2}Be{sub 2}O{sub 3} for high-functional tritium breeders

Energy Technology Data Exchange (ETDEWEB)

Hoshino, Tsuyoshi, E-mail: hoshino.tsuyoshi@jaea.go.jp [Breeding Functional Materials Development Group, Fusion Research and Development Directorate, Japan Atomic Energy Agency, 2-166, Obuchi, Omotedate, Rokkasho-mura, Kamikita-gun, Aomori 039-3212 (Japan); Oikawa, Fumiaki [Breeding Functional Materials Development Group, Fusion Research and Development Directorate, Japan Atomic Energy Agency, 2-166, Obuchi, Omotedate, Rokkasho-mura, Kamikita-gun, Aomori 039-3212 (Japan); Natori, Yuri; Kato, Kenichi; Sakka, Tomoko; Nakamura, Mutsumi; Tatenuma, Katsuyoshi [Kaken, Co. Ltd., 1044, Hori, Mito-city, Ibaraki 310-0903 (Japan)

2013-10-15

Highlights: • Mixtures of tritium breeder and neutron multiplier (Be or Be{sub 12}Ti) pebbles are being considered for increasing the tritium breeding ratio in DEMO blankets. • A high-functional tritium breeder such as lithium beryllium oxide (Li{sub 2}Be{sub 2}O{sub 3}) needs to be developed to compensate for this reaction under high-temperatures. • Solid-state reaction of LiOH·H{sub 2}O and BeO is well-suited for synthesizing Li{sub 2}Be{sub 2}O{sub 3}. • The optimum sintering temperature was selected from 1000 K to 1273 K by TG–DTA. -- Abstract: Mixtures of tritium breeder (lithium) and neutron multiplier (beryllium) are being considered for use in increasing the tritium breeding ratio in breeding blankets. However, lithium and beryllium react under normal operating conditions, and therefore, a high-functional tritium breeder such as lithium beryllium oxide (Li{sub 2}Be{sub 2}O{sub 3}) needs to be developed to compensate for this reaction under high-temperatures. LiOH·H{sub 2}O and BeO powders were mixed in stoichiometric proportions at a Li/Be molecular ratio of 1.0. The sintering temperature was established as 1073 K by thermogravimetric/differential thermal analysis (TG–DTA). The Li/Be molar ratio of the reaction products measured by inductively coupled plasma atomic emission spectroscopy (ICP-AES) after the reaction agreed with the nominal molar ratio obtained by mixing LiOH·H{sub 2}O and BeO. Crystal structure analysis of this powder was performed by the XRD technique. The XRD patterns of products were the same as those of Li{sub 2}Be{sub 2}O{sub 3} as listed in the JC-PDF-Card, and no impurities were indicated. The results indicate that the solid-state reaction of LiOH·H{sub 2}O and BeO is suitable for synthesizing lithium beryllium oxide (Li{sub 2}Be{sub 2}O{sub 3})

Solution based synthesis of mixed-phase materials in the Li{sub 2}TiO{sub 3}–Li{sub 4}SiO{sub 4} system

Energy Technology Data Exchange (ETDEWEB)

Hanaor, Dorian A.H., E-mail: dorian.hanaor@sydney.edu.au [School of Civil Engineering, University of Sydney, NSW 2006 (Australia); Kolb, Matthias H.H. [Institute for Applied Materials, Karlsruhe Institute of Technology, 76021 (Germany); Gan, Yixiang [School of Civil Engineering, University of Sydney, NSW 2006 (Australia); Kamlah, Marc; Knitter, Regina [Institute for Applied Materials, Karlsruhe Institute of Technology, 76021 (Germany)

2015-01-15

Highlights: • Investigation of phase stability in the quasi-binary Li{sub 2}TiO{sub 3}–Li{sub 4}SiO{sub 4} system. • Sol-based syntheses of mixed phase materials from organometallic precursors. • LiCl based synthesis results in greater lithium deficiency than LiOH synthesis. • The Li{sub 2}TiO{sub 3}–Li{sub 4}SiO{sub 4} quasi binary system appears to exhibit monotectic behaviour. • Mixed phase materials show liquid formation from melting of silicate material at 1100 °C. - Abstract: As candidate tritium breeder materials for use in the ITER helium cooled pebble bed, ceramic multiphasic compounds lying in the region of the quasi-binary lithium metatitanate–lithium orthosilicate system may exhibit mechanical and physical advantages relative to single phase materials. Here we present an organometallic solution-based synthesis procedure for the low-temperature fabrication of compounds in the Li{sub 2}TiO{sub 3}–Li{sub 4}SiO{sub 4} region and investigate phase stability and transformations through temperature varied X-ray diffraction and scanning calorimetry. Results demonstrate that the metatitanate and metasilicate phases Li{sub 2}TiO{sub 3} and Li{sub 2}SiO{sub 3} readily crystallise in nanocrystalline form at temperatures below 180 °C. Lithium deficiency in the region of 5% results from Li sublimation from Li{sub 4}SiO{sub 4} and/or from excess Li incorporation in the metatitanate phase and brings about a stoichiometry shift, with product compounds exhibiting mixed lithium orthosilicate/metasilicate content towards the Si rich region and predominantly Li{sub 2}TiO{sub 3} content towards the Ti rich region. Above 1150 °C the transformation of monoclinic to cubic γ-Li{sub 2}TiO{sub 3} disordered solid-solution occurs while the melting of silicate phases indicates a likely monotectic type system with a solidus line in the region 1050–1100 °C. Synthesis procedures involving a lithium chloride precursor are not likely to be a viable option for

Reaction kinetics aspect of U3O8 kernel with gas H2 on the characteristics of activation energy, reaction rate constant and O/U ratio of UO2 kernel

International Nuclear Information System (INIS)

Damunir

2007-01-01

The reaction kinetics aspect of U 3 O 8 kernel with gas H 2 on the characteristics of activation energy, reaction rate constant and O/U ratio of UO 2 kernel had been studied. U 3 O 8 kernel was reacted with gas H 2 in a reduction furnace at varied reaction time and temperature. The reaction temperature was varied at 600, 700, 750 and 850 °C with a pressure of 50 mmHg for 3 hours in gas N 2 atmosphere. The reation time was varied at 1, 2, 3 and 4 hours at a temperature of 750 °C using similar conditions. The reaction product was UO 2 kernel. The reaction kinetic aspect between U 3 O 8 and gas H 2 comprised the minimum activation energy (ΔE), the reaction rate constant and the O/U ratio of UO 2 kernel. The minimum activation energy was determined from a straight line slope of equation ln [{D b . R o {(1 - (1 - X b ) ⅓ } / (b.t.Cg)] = -3.9406 x 10 3 / T + 4.044. By multiplying with the straight line slope -3.9406 x 10 3 , the ideal gas constant (R) 1.985 cal/mol and the molarity difference of reaction coefficient 2, a minimum activation energy of 15.644 kcal/mol was obtained. The reaction rate constant was determined from first-order chemical reaction control and Arrhenius equation. The O/U ratio of UO 2 kernel was obtained using gravimetric method. The analysis result of reaction rate constant with chemical reaction control equation yielded reaction rate constants of 0.745 - 1.671 s -1 and the Arrhenius equation at temperatures of 650 - 850 °C yielded reaction rate constants of 0.637 - 2.914 s -1 . The O/U ratios of UO 2 kernel at the respective reaction rate constants were 2.013 - 2.014 and the O/U ratios at reaction time 1 - 4 hours were 2.04 - 2.011. The experiment results indicated that the minimum activation energy influenced the rate constant of first-order reaction and the O/U ratio of UO 2 kernel. The optimum condition was obtained at reaction rate constant of 1.43 s -1 , O/U ratio of UO 2 kernel of 2.01 at temperature of 750 °C and reaction time of 3

A note on structural and dielectric properties of BiFeO3- PbTiO3 and BiFeO3- PbZrO3 composites

International Nuclear Information System (INIS)

Satpathy, S. K.; Mohanty, N. K.; Behera, A. K.; Behera, B.; Nayak, P.

2015-01-01

The composites of BiFeO 3 -PbTiO 3 (BF-PT) and BiFeO 3 -PbZrO 3 (BF-PZ) were prepared by mixed oxide method. Room temperature X-ray diffraction data confirms the rhombohedral and tetragonal crystal structure respectively. Dielectric constant of BF-PZ is found to give high value compared to BF-PT and hence, there is an increase value of ac conductivity for the former. Both the composites show negative temperature coefficient of resistance (NTCR) behavior. The activation energies of BF-PT and BF-PZ are found to be 0.35 eV and 0.53 eV respectively. The d 33 coefficients are found to be 2.0 and 2.1 pC/N for BF-PT and BF-PZ respectively

Mixed Matrix Carbon Molecular Sieve and Alumina (CMS-Al2O3) Membranes.

Science.gov (United States)

Song, Yingjun; Wang, David K; Birkett, Greg; Martens, Wayde; Duke, Mikel C; Smart, Simon; Diniz da Costa, João C

2016-07-29

This work shows mixed matrix inorganic membranes prepared by the vacuum-assisted impregnation method, where phenolic resin precursors filled the pore of α-alumina substrates. Upon carbonisation, the phenolic resin decomposed into several fragments derived from the backbone of the resin matrix. The final stages of decomposition (>650 °C) led to a formation of carbon molecular sieve (CMS) structures, reaching the lowest average pore sizes of ~5 Å at carbonisation temperatures of 700 °C. The combination of vacuum-assisted impregnation and carbonisation led to the formation of mixed matrix of CMS and α-alumina particles (CMS-Al2O3) in a single membrane. These membranes were tested for pervaporative desalination and gave very high water fluxes of up to 25 kg m(-2) h(-1) for seawater (NaCl 3.5 wt%) at 75 °C. Salt rejection was also very high varying between 93-99% depending on temperature and feed salt concentration. Interestingly, the water fluxes remained almost constant and were not affected as feed salt concentration increased from 0.3, 1 and 3.5 wt%.

Fabrication of high aspect ratio TiO{sub 2} and Al{sub 2}O{sub 3} nanogratings by atomic layer deposition

Energy Technology Data Exchange (ETDEWEB)

Shkondin, Evgeniy, E-mail: eves@fotonik.dtu.dk [Department of Photonics Engineering, Technical University of Denmark, DK-2800 Kongens Lyngby, Denmark and Danish National Center for Micro- and Nanofabrication (DANCHIP), DK-2800 Kongens Lyngby (Denmark); Takayama, Osamu; Lavrinenko, Andrei V. [Department of Photonics Engineering, Technical University of Denmark, DK-2800 Kongens Lyngby (Denmark); Lindhard, Jonas Michael; Larsen, Pernille Voss; Mar, Mikkel Dysseholm; Jensen, Flemming [Danish National Center for Micro- and Nanofabrication (DANCHIP), DK-2800 Kongens Lyngby (Denmark)

2016-05-15

The authors report on the fabrication of TiO{sub 2} and Al{sub 2}O{sub 3} nanostructured gratings with an aspect ratio of up to 50. The gratings were made by a combination of atomic layer deposition (ALD) and dry etch techniques. The workflow included fabrication of a Si template using deep reactive ion etching followed by ALD of TiO{sub 2} or Al{sub 2}O{sub 3}. Then, the template was etched away using SF{sub 6} in an inductively coupled plasma tool, which resulted in the formation of isolated ALD coatings, thereby achieving high aspect ratio grating structures. SF{sub 6} plasma removes silicon selectively without any observable influence on TiO{sub 2} or Al{sub 2}O{sub 3}, thus revealing high selectivity throughout the fabrication. Scanning electron microscopy was used to analyze every fabrication step. Due to nonreleased stress in the ALD coatings, the top parts of the gratings were observed to bend inward as the Si template was removed, thus resulting in a gradual change in the pitch value of the structures. The pitch on top of the gratings is 400 nm, and it gradually reduces to 200 nm at the bottom. The form of the bending can be reshaped by Ar{sup +} ion beam etching. The chemical purity of the ALD grown materials was analyzed by x-ray photoelectron spectroscopy. The approach presented opens the possibility to fabricate high quality optical metamaterials and functional nanostructures.

X-ray fluorescence analysis of Cr6+ component in mixtures of Cr2O3 and K2CrO4

International Nuclear Information System (INIS)

Tochio, Tatsunori; Sakakura, Shusuke; Oohashi, Hirofumi

2010-01-01

X-ray fluorescence analysis using Cr K α spectra was applied to the determination of the mixing ratio of Cr 6+ to (Cr 6+ + Cr 3+ ) in several mixtures of K 2 CrO 4 and Cr 2 O 3 . Because the powder of K 2 CrO 4 contained large particles that were more than 50 μm in diameter, it was ground between a pestle and a mortar for about 8 h. The coarse particles still remaining were removed by using a sieve with 325-mesh (44 μm) in order to reduce the difference in absorption effects between emissions from Cr 6+ and those from Cr 3+ . The mixing ratio, K 2 CrO 4 /(K 2 CrO 4 + Cr 2 O 3 ), of the five mixtures investigated is 0.50, 0.40, 0.20, 0.10, and 0.05 in weight, respectively. Each spectrum obtained was analyzed by decomposing it into two reference spectra, those of the two pure materials, K 2 CrO 4 and Cr 2 O 3 , with a constant background. The results for the mixtures containing K 2 CrO 4 of more than 20 wt% are that the relative deviation from the true value is less than ∼5%. On the other hand, when the content of K 2 CrO 4 decreases to less than 10 wt%, the relative deviation gets so large as 20 - 25%. The error coming from a peak separation of spectrum involved in our results were estimated by applying our method to five sets of data for each mixture computationally generated, taking into account the uncertainty in total counts of real measurements. (author)

X-ray fluorescence analysis of Cr(6+) component in mixtures of Cr(2)O(3) and K(2)CrO(4).

Science.gov (United States)

Tochio, Tatsunori; Sakakura, Shusuke; Oohashi, Hirofumi; Mizota, Hirohisa; Zou, Yanhui; Ito, Yoshiaki; Fukushima, Sei; Tanuma, Shigeo; Shoji, Takashi; Fujimura, Hajime; Yamashita, Michiru

2010-01-01

X-ray fluorescence analysis using Cr K(alpha) spectra was applied to the determination of the mixing ratio of Cr(6+) to (Cr(6+) + Cr(3+)) in several mixtures of K(2)CrO(4) and Cr(2)O(3). Because the powder of K(2)CrO(4) contained large particles that were more than 50 microm in diameter, it was ground between a pestle and a mortar for about 8 h. The coarse particles still remaining were removed by using a sieve with 325-mesh (44 microm) in order to reduce the difference in absorption effects between emissions from Cr(6+) and those from Cr(3+). The mixing ratio, K(2)CrO(4)/(K(2)CrO(4) + Cr(2)O(3)), of the five mixtures investigated is 0.50, 0.40, 0.20, 0.10, and 0.05 in weight, respectively. Each spectrum obtained was analyzed by decomposing it into two reference spectra, those of the two pure materials, K(2)CrO(4) and Cr(2)O(3), with a constant background. The results for the mixtures containing K(2)CrO(4) of more than 20 wt% are that the relative deviation from the true value is less than approximately 5%. On the other hand, when the content of K(2)CrO(4) decreases to less than 10 wt%, the relative deviation gets so large as 20 - 25%. The error coming from a peak separation of spectrum involved in our results were estimated by applying our method to five sets of data for each mixture computationally generated, taking into account the uncertainty in total counts of real measurements.

3He/4He production ratios by tetrahedral symmetric condensation

International Nuclear Information System (INIS)

Takahashi, Akito

2006-01-01

The present paper treats application of the Electronic Quasi-Particle Expansion Theory (EQPET) model for Tetrahedral Symmetric Condensate (TSC) of H/D mixed systems for Pd host metal. Production ratios of 3 He/ 4 He for multi-body fusion reactions in H/D mixed TSC systems are calculated as a function of H/D mixing ratio. The model is further extended to treat direct nuclear interactions between host-metal nucleus and TSC of pure four protons (or four deuterons), since TSC can become very small (far less than 1 pm radius) charge-neutral pseudo-particle. Results for the case of Ni + 4p/TSC are discussed with Ni + p capture reactions and Ni + 4p fission reactions. (authors)

Mixed oxides forming in CdO-OsO2 and PbO-OsO2 systems

International Nuclear Information System (INIS)

Shaplygin, I.S.; Lazarev, V.B.

1978-01-01

The formation of mixed oxides in systems CdO-OsO 2 and PbO-OsO 2 was studied by derivatography, X-ray phase analysis, and IR spectroscopy. It was established that in the system CdO-OsO 2 cubic phases of Cdsub(2)Ossub(2)Osub(6.7) and Cdsub(2)Ossub(2)Osub(7.2) with a pyrochlor-type structure, as well as new compounds with the structure of rhombic perovskite CdOsO 3 and Cd(Cdsub(0.5)Ossub(0.5))Osub(3) containing osmium in the formal degree of oxidation +4 and +6, respectively, are formed. The thermal stability of the compounds obtained was studied and their electrical properties determined

Direct Dynamics Simulation of the Thermal 3CH2 + 3O2 Reaction. Rate Constant and Product Branching Ratios.

Science.gov (United States)

Lakshmanan, Sandhiya; Pratihar, Subha; Machado, Francisco Bolivar Correto; Hase, William Louis

2018-04-26

The reaction of 3CH2 with 3O2 is of fundamental importance in combustion and the reaction is complex as a result of multiple extremely exothermic product channels. In the present study, direct dynamics simulations were performed to study the reaction on both the singlet and triplet potential energy surfaces (PESs). The simulations were performed at the UM06/6-311++G(d,p) level of theory. Trajectories were calculated at a temperature of 300 K and all reactive trajectories proceeded through the carbonyl oxide Criegee intermediate, CH2OO, on both the singlet and triplet PESs. The triplet surface leads to only one product channel, H2CO + O(3P), while the singlet surface leads to 8 product channels with their relative importance as: CO + H2O > CO + OH + H ~ H2CO + O(1D) > HCO + OH ~ CO2 + H2 ~ CO + H2 + O(1D) > CO2 + H + H > HCO + O(1D) + H. Reaction on the singlet PES is barrierless, consistent with experiment and the total rate constant on the singlet surface is 0.93 ± 0.22 x 10-12 cm3molecule-1s-1 in comparison to the recommended experimental rate constant of 3.3 x 10-12 cm3molecule-1s-1. The simulation product yields for the singlet PES are compared with experiment and the most significant differences are for H, CO2, and H2O. Reaction on the triplet surface is also barrierless, inconsistent with experiment. A discussion is given of the need for future calculations to address the: (1) barrier on the triplet PES for 3CH2 + 3O2 → 3CH2OO; (2) temperature dependence of the 3CH2 + 3O2 reaction rate constant and product branching ratios; and (3) possible non-RRKM dynamics of the 1CH2OO Criegee intermediate.

Aurivillius-Popper mixed superconductors in BiO--CuO--(Sr/sub 0.5/, Ca/sub 0.5/)O system

International Nuclear Information System (INIS)

Fukuhara, M.; Bhalla, A.S.; Mulay, L.N.; Newnham, R.E.

1989-01-01

We report the effect of inhomogeneities on the electric resistivity and ac magnetic susceptibility in Aurivillius-like bismuth mixed phase oxides of the BiO--Cuo--(Sr/sub 0.5/, Ca/sub 0.5/)O system and propose a crystal structure of the major phase having highest T/sub c/. Nominal Aurivillius compositions with molar ratios of BiO/(Sr/sub 0.5/, Ca/sub 0.5/)O = 1/2 are superconductors with T/sub c/ ranging from 83 to 107 K, and are accompanied by a large expansion during sintering due to the formation of Kirkendall voids. T/sub c/ increases with decreasing of the c lattice parameter. An oxide BiSrCaCu 2 O/sub x/ (n = 2) shows a maximum T/sub c/ value of 107 K and an onset of superconductivity at a much higher temperature. It seems that the structure of Bi 2 Sr 2 CaCu 2 O/sub x/ consists of an Aurivillius-like phase having two perovskite layers and a Popper mixed phase. The ac magnetic susceptibility showed an overall decrease in susceptibility with time up to 220 days. This appears to be related to the relief of intralattice strain

Investigation of phase relationships in subsolidus region of Ln2O3-MoO3-B2O3 systems

International Nuclear Information System (INIS)

Lysanova, C.V.; Dzhurinskij, B.F.; Komova, M.G.; Tananaev, I.V.

1983-01-01

Phase formation in subsolidus region of Ln 2 O 3 -MoO 3 B 2 O 3 systems (Ln-La, Nd) is studied. Three compounds with mixed oxyanions-boratomolybdates of LnMoBO 6 composition (Ln-La, Ce, Pr, Nd), Ln 2 MoB 2 O 9 (Ln-La, Ce, Pr, Nd, Sm, EU, Gde Tb) Ln 6 Mo 3 B 4 0 24 (Ln-Pr, Nd) are revealed and described

Effective role of CaO/P2O5 ratio on SiO2-CaO-P2O5 glass system

Directory of Open Access Journals (Sweden)

P. Kiran

2017-05-01

Full Text Available In the present work, the effect of the CaO/P2O5 ratio on the composition of sol-gel synthesized 58SiO2-(19 − xP2O5–(23 + xCaO (x = 0, 5, 10 and 15 mol% glass samples was studied. Further, the effect of NBO/BO ratio on hydroxy carbonated apatite layer (HCA forming ability based on dissolution behavior in simulated body fluid (SBF solution was also investigated. CaO/P2O5 ratios of synthesized glass samples were 1.2, 2, 3.6, and 9.5, respectively. NBO/BO ratios were obtained using Raman spectroscopic analysis as 0.58, 1.20, 1.46, and 1.78, respectively. All samples were soaked in the SBF solution for 7 days. The calculated weight losses of these samples were 58%, 64%, 83%, and 89% for corresponding NBO/BO ratios. The increase in CaO/P2O5 ratio increases the NBO/BO ratios. However, the increase in NBO/BO ratio increases HCA forming ability of SBF treated samples. The HCA crystalline layer formation was confirmed through X-ray Diffraction (XRD, Transmission Electron Microscopy (TEM, Scanning Electron Microscopy (SEM, Raman and Infrared spectroscopic analysis. Higher CaO/P2O5 ratio favors the increase in HCA formation for SBF treated calcium phospho silicate glasses.

The decomposition of mixed oxide Ag2Cu2O3: Structural features and the catalytic properties in CO and C2H4 oxidation

Science.gov (United States)

Svintsitskiy, Dmitry A.; Kardash, Tatyana Yu.; Slavinskaya, Elena M.; Stonkus, Olga A.; Koscheev, Sergei V.; Boronin, Andrei I.

2018-01-01

The mixed silver-copper oxide Ag2Cu2O3 with a paramelaconite crystal structure is a promising material for catalytic applications. The as-prepared sample of Ag2Cu2O3 consisted of brick-like particles extended along the [001] direction. A combination of physicochemical techniques such as TEM, XPS and XRD was applied to investigate the structural features of this mixed silver-copper oxide. The thermal stability of Ag2Cu2O3 was investigated using in situ XRD under different reaction conditions, including a catalytic CO + O2 mixture. The first step of Ag2Cu2O3 decomposition was accompanied by the appearance of ensembles consisting of silver nanoparticles with sizes of 5-15 nm. Silver nanoparticles were strongly oriented to each other and to the surface of the initial Ag2Cu2O3 bricks. Based on the XRD data, it was shown that the release of silver occurred along the a and b axes of the paramelaconite structure. Partial decomposition of Ag2Cu2O3 accompanied by the formation of silver nanoparticles was observed during prolonged air storage under ambient conditions. The high reactivity is discussed as a reason for spontaneous decomposition during Ag2Cu2O3 storage. The full decomposition of the mixed oxide into metallic silver and copper (II) oxide took place at temperatures higher than 300 °C regardless of the nature of the reaction medium (helium, air, CO + O2). Catalytic properties of partially and fully decomposed samples of mixed silver-copper oxide were measured in low-temperature CO oxidation and C2H4 epoxidation reactions.

Influence of Li/Nb ratios on defect structure and photorefractive properties of Zn: In: Fe: LiNbO 3 crystals

Science.gov (United States)

Dai, Li; Su, Yan-Qing; Wu, Shi-Ping; Guo, Jing-Jie; Xu, Chao; Xu, Yu-Heng

2011-04-01

A series of Zn: In: Fe: LiNbO3 crystals are grown by the Czochralski technique with various ratios of Li/Nb = 0.94, 1.05, 1.20 and 1.38 in the melt. The Zn, In, Fe, Nb and Li concentrations in the crystals are analyzed by inductively coupled plasma (ICP) spectrometry. The results indicate that with increasing the [Li]/[Nb] ratio in melt, [Li]/[Nb] ratio increases and goes up continuously in the crystal, the segregation coefficients of both Zn and In ions decrease. The absorption spectra measurement and two-wave coupling experiment are employed to study the effect of [Li]/[Nb] ratio on photorefractive properties of Zn: In: Fe: LiNbO3 crystals. It is found that the [Li]/[Nb] ratio increases, the write time is shortened and the photorefractive sensitivity is improved.

Interactions of a La{sub O.9}Sr{sub O.1}Ga{sub O.8}Mg{sub O.2}O{sub 3-{delta}} electrolyte with Fe{sub 2}O{sub 3}, Co{sub 2}O{sub 3} and NiO anode materials

Energy Technology Data Exchange (ETDEWEB)

Zhang, X.; Ohara, S.; Okawa, H.; Maric, R.; Fukui, T. [Japan Fine Ceramics Center, 2-4-1 Mutsuo, Atsuta-ku, 456-8587 Nagoya (Japan)

2001-01-02

In this study, the interactions of a Sr- and Mg-doped lanthanum gallate (LSGM with composition La{sub O.9}Sr{sub O.1}Ga{sub O.8}Mg{sub O.2}O{sub 3-{delta}}) electrolyte with Fe{sub 2}O{sub 3}, Co{sub 2}O{sub 3} and NiO as the anode starting materials were investigated. It was found that the order of reactivity of the LSGM with the three oxides was Co{sub 2}O{sub 3}>NiO>Fe{sub 2}O{sub 3}, and La-containing oxides were detected in these binary powder mixtures after firing. The anode performance was greatly influenced by the interaction. The Fe{sub 2}O{sub 3}-LSGM anode, mixed with 40 vol.% LSGM powder and sintered at 1150C, exhibited the highest initial performance in comparison with NiO-LSGM and Co{sub 2}O{sub 3}-LSGM anodes. It seems that Fe{sub 2}O{sub 3} is a possible anode starting material for a LSGM-based solid oxide fuel cell.

Effects of dopant ion and Mn valence state in the La1-xAxMnO3 (A=Sr,Ba) colossal magnetoresistance films

International Nuclear Information System (INIS)

Choi, Sun Gyu; Wang, Seok-Joo; Park, Hyung-Ho; Hong, MunPyo; Kwon, Kwang-Ho

2010-01-01

The structural and electrical properties of Mn-based colossal magnetoresistance (CMR) thin films with controlled tolerance factor and Mn ion valance ratio were studied using crystal structure and chemical bonding character analyses. La 0.7 Sr 0.3 MnO 3 , La 0.7 Ba 0.3 MnO 3 , and La 0.82 Ba 0.18 MnO 3 thin films with different contents of divalent cations and Mn 3+ /Mn 4+ ratios were deposited on amorphous SiO 2 /Si substrate by rf magnetron sputtering at a substrate temperature of 350 deg. C. The films showed the same crystalline structure as the pseudocubic structure. The change in the sheet resistance of films was analyzed according to strain state of the unit cell, chemical bonding character of Mn-O, and Mn 3+ /Mn 4+ ratio controlling the Mn 3+ -O 2- -Mn 4+ conducting path. Mn L-edge x-ray absorption spectra revealed that the Mn 3+ /Mn 4+ ratio changed according to different compositions of Sr or Ba and the Mn 2p core level x-ray photoelectron spectra showed that the Mn 2p binding energy was affected by the covalence of the Mn-O bond and Mn 3+ /Mn 4+ ratio. In addition, O K-edge x-ray absorption spectra showed covalently mixed Mn 3d and O 2p states and matched well with the resistivity changes of CMR films. Temperature coefficient of resistance values were obtained at approximately -2.16%/K to -2.46%/K of the CMR films and were correct for infrared sensor applications.

Study of UO2-10WT%Gd2O3 fuel pellets obtained by seeding method using AUC co-precipitation and mechanical mixing processes

International Nuclear Information System (INIS)

Lima, M.M.F.; Ferraz, W.B.A.; Santos, M.M. dos; Pinto, L.C.M.; Santos, A.

2008-01-01

The use of gadolinium and uranium mixed oxide as a nuclear fuel aims to obtain a fuel with a performance better than that of UO 2 fuel. In this work, seeding method was used to improve ionic diffusivity during sintering to produce high density pellets containing coarse grains by co-precipitation and mechanical mixing processes. Sintered UO 2 -10 wt% Gd 2 O 3 pellets were obtained using the reference processes with 2 wt% and 5 wt% UO 2 seeds with two granulometries, less than 20 μm and between 20 and 38 μm. Characterisation was carried out by chemical analysis, surface area, X-ray diffraction, SEM, WDS, image analysis, and densitometry. The seeding method using mechanical mixing process was more effective than the co-precipitation method. Furthermore, mechanical mixing process resulted in an increase in density of UO 2 -10wt% Gd 2 O 3 with seeds in relation to that of UO 2 -10wt% Gd 2 O 3 without seeds. (author)

Variation of the 18O/16O ratio in water samples from branches

International Nuclear Information System (INIS)

Foerstel, H.; Huetzen, H.

1979-06-01

The studies of the water turnover of plants may use the labelling of water by its natural variation of the 18 O/ 16 O ratio. The basic value of such a study is the isotope ratio in soil water, which is represented by the 18 O/ 16 O ratio in water samples from stem and branches, too. During the water transport from the soil water reservoir to the leaves of trees, no fractionation of the oxygen isotopes occurs. The oxygen isotope ratio within a single twig varies about +- 0 / 00 (variation given as standard deviation of the delta-values), within the stem of a large tree about +- 2 0 / 00 . The results of water from stems of different trees at the site of the Nuclear Research Center Juelich scatter about +- 1 0 / 00 . The delta-values from a larger area (Rur valley-Eifel hills-Mosel valley), which were collected in October 1978 during the end of the vegetation period, showed a standard deviation between +- 2.2 (Rur valley) and +- 3.6 0 / 00 (Eifel hills). The 18 O/ 16 O-delta-values of a beech wood from Juelich site are in the range of - 7.3 and - 10.1 0 / 00 (mean local precipitation 1974 - 1977: - 7.4 0 / 00 ). At the hill site near Cologne (Bergisches Land, late September 1978) we observed an oxygen isotope ratio of - 9.1 0 / 00 (groundwater at the neighbourhood between - 7.6 and 8.7 0 / 00 ). In October 1978 at an area from the Netherlands to the Mosel valley we found delta-values of branch water between - 13.9 (lower Ruhr valley) and - 13.1 (Eifel hills to Mosel valley) in comparison to groundwater samples from the same region: - 7.55 and - 8.39. There was no significant difference between delta-values from various species or locations within this area. Groundwater samples should normally represent the 18 O/ 16 O ratio of local precipitation. The low delta-values of branch water could be due to the rapid uptake of precipitation water of low 18 O content in autumn to the water transport system of plants. (orig.) [de

Effect of metal ratio and calcination temperature of chromium based mixed oxides catalyst on FAME density from palm fatty acid distillate

Science.gov (United States)

Wan, Z.; Fatimah, S.; Shahar, S.; Noor, A. C.

2017-09-01

Mixed oxides chromium based catalysts were synthesized via sol-gel method for the esterification of palm fatty acid distillate (PFAD) to produce fatty acid methyl ester (FAME). The reactions were conducted in a batch reactor at reaction temperature of 160 °C for 4 h and methanol to PFAD molar ratio of 3:1. The effects of catalyst preparation conditions which are the mixed metal ratio and calcination temperature were studied. The various metal ratio of Cr:Mn (1:0, 0:1, 1:1, 1:2 and 2:1) and Cr:Ti (0:1, 1:1, 1:2 and 2:1) resulted in FAME density ranges from 1.041 g/cm3 to 0.853 g/cm3 and 1.107 g/cm3 to 0.836 g/cm3, respectively. The best condition catalyst was found to be Cr:Ti metal ratio of 1:2 and Cr:Mn metal ratio of 1:1. The calcination temperature of the mixed oxides between 300 °C to 700°C shows effect on the FAME density obtained in the reaction. The calcination at 500°C gave the lowest FAME density of 0.836 g/cm3 and 0.853 g/cm3 for Cr:Ti and Cr:Mn mixed oxides, respectively. The density of FAME is within the value range of the biodiesel fuel property. Thus, mixed oxides of Cr-Ti and Cr-Mn have good potentials as heterogeneous catalyst for FAME synthesis from high acid value oils such as PFAD.

Contrasting winter and summer VOC mixing ratios at a forest site in the Western Mediterranean Basin: the effect of local biogenic emissions

Directory of Open Access Journals (Sweden)

R. Seco

2011-12-01

Full Text Available Atmospheric volatile organic compounds (VOCs are involved in ozone and aerosol generation, thus having implications for air quality and climate. VOCs and their emissions by vegetation also have important ecological roles as they can protect plants from stresses and act as communication cues between plants and between plants and animals. In spite of these key environmental and biological roles, the reports on seasonal and daily VOC mixing ratios in the literature for Mediterranean natural environments are scarce.

We conducted seasonal (winter and summer measurements of VOC mixing ratios in an elevated (720 m a.s.l. holm oak Mediterranean forest site near the metropolitan area of Barcelona (NE Iberian Peninsula. Methanol was the most abundant compound among all the VOCs measured in both seasons. While aromatic VOCs showed almost no seasonal variability, short-chain oxygenated VOCs presented higher mixing ratios in summer, presumably due to greater emission by vegetation and increased photochemistry, both enhanced by the high temperatures and solar radiation in summer. Isoprenoid VOCs showed the biggest seasonal change in mixing ratios: they increased by one order of magnitude in summer, as a result of the vegetation's greater physiological activity and emission rates. The maximum diurnal concentrations of ozone increased in summer too, most likely due to more intense photochemical activity and the higher levels of VOCs in the air.

The daily variation of VOC mixing ratios was mainly governed by the wind regime of the mountain, as the majority of the VOC species analyzed followed a very similar diel cycle. Mountain and sea breezes that develop after sunrise advect polluted air masses to the mountain. These polluted air masses had previously passed over the urban and industrial areas surrounding the Barcelona metropolitan area, where they were enriched in NO_x and in VOCs of biotic and abiotic origin. Moreover, these

Anelastic anomalies and negative Poisson's ratio in tetragonal BaTiO3 ceramics

International Nuclear Information System (INIS)

Dong Liang; Stone, Donald S.; Lakes, Roderic S.

2010-01-01

Anelastic anomalies (sharp variations in modulus and damping with temperature) were observed in tetragonal BaTiO 3 via broadband viscoelastic spectroscopy after aging at 50 deg. C for 15 h. The effect was most pronounced under electrical short circuit condition, at low frequency and under small excitation strain (10 -6 ). Softening in bulk modulus and negative Poisson's ratio were observed near 60 deg. C. Effects are attributed to an oxygen vacancy mechanism. A relaxational model cannot account for sharp response at smaller strains. Heterogeneity of negative stiffness is considered as a cause.

Sequential Condensation and Hydrodeoxygenation Reaction of Furfural-Acetone Adduct over Mix Catalysts Ni/SiO2 and Cu/SiO2 in Water

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Siti Mariyah Ulfa

2018-05-01

Full Text Available Sequential condensation and hydrodeoxygenation reaction were perform using autoclave batch reactor in the presence of water as a solvent. The condensation of furfural and acetone was performed using MgO catalyst followed by hydrodeoxygenation using mix catalyst Ni/SiO2 and Cu/SiO2. The catalyst was prepared by wet-impregnation method and analyzed by XRD, SEM-EDX as well as BET surface. Condensation of furfural and acetone in 1:2 mol ratio was carried out by reflux gave 4-(2-furyl-3-buten-2-one and 1,5-bis-(2-furanyl-1,4-pentadien-3-one. The condensation product was then subjected for hydrodeoxygenation using batch reactor, catalyzed by mixed Ni/SiO2 and Cu/SiO2 at 150 and 180 °C for 2 h. The product identified as alkane derivatives with the conversion at 38.83 and 50.35%, respectively. The selectivity of hydrocarbon is 61.39% at 150 °C and 16.55% at 180 °C. Increasing the reaction temperature to 200 °C did not give any products except the recovery of the precursor. It showed that higher temperature enhanced the catalyst activity but the selectivity is controlled by low reaction temperature.

Large eddy simulation of reactive pollutants in a deep urban street canyon: Coupling dynamics with O3-NOx-VOC chemistry.

Science.gov (United States)

Zhong, Jian; Cai, Xiao-Ming; Bloss, William James

2017-05-01

A large eddy simulation (LES) model coupled with O 3 -NO x -VOC chemistry is implemented to simulate the coupled effects of emissions, mixing and chemical pre-processing within an idealised deep (aspect ratio = 2) urban street canyon under a weak wind condition. Reactive pollutants exhibit significant spatial variations in the presence of two vertically aligned unsteady vortices formed in the canyon. Comparison of the LES results from two chemical schemes (simple NO x -O 3 chemistry and a more comprehensive Reduced Chemical Scheme (RCS) chemical mechanism) shows that the concentrations of NO 2 and O x inside the street canyon are enhanced by approximately 30-40% via OH/HO 2 chemistry. NO, NO x , O 3 , OH and HO 2 are chemically consumed, while NO 2 and O x (total oxidant) are chemically produced within the canyon environment. Within-canyon pre-processing increases oxidant fluxes from the canyon to the overlying boundary layer, and this effect is greater for deeper street canyons (as found in many traditional European urban centres) than shallower (lower aspect ratio) streets. There is clear evidence of distinct behaviours for emitted chemical species and entrained chemical species, and positive (or negative) values of intensities of segregations are found between pairs of species with similar (or opposite) behaviour. The simplified two-box model underestimated NO and O 3 levels, but overestimated NO 2 levels for both the lower and upper canyon compared with the more realistic LES-chemistry model. This suggests that the segregation effect due to incomplete mixing reduces the chemical conversion rate of NO to NO 2 . This study reveals the impacts of nonlinear O 3 -NO x -VOC photochemical processes in the incomplete mixing environment and provides a better understanding of the pre-processing of emissions within canyons, prior to their release to the urban boundary layer, through the coupling of street canyon dynamics and chemistry. Copyright © 2017 Elsevier Ltd

Enhanced Ga2O3-photocatalyzed and photochemical degradation of the Fipronil insecticide by UVC irradiation in mixed aqueous/organic media under an inert atmosphere.

Science.gov (United States)

Hidaka, Hisao; Tsukamoto, Tohru; Mitsutsuka, Yoshihiro; Oyama, Toshiyuki; Serpone, Nick

2015-05-01

Agrochemicals such as the insecticide Fipronil that bear fluoro groups are generally fat-soluble and nearly insoluble in water, so that their photodegradation in a heterogeneous aqueous gallium oxide dispersion presents some challenges. This article examined the photodegradation of this insecticide by solubilizing it through the addition of organic solvents (EtOH, MeOH, THF, 1,4-dioxane and ethylene glycol) to an aqueous medium and then subjecting the insecticide to 254 nm UVC radiation under photocatalytically inert (Ga2O3/N2) and air-equilibrated (Ga2O3/O2) conditions, as well as photochemically in the absence of Ga2O3 but also under inert and air-equilibrated conditions. Defluorination, dechlorination, desulfonation and denitridation of Fipronil were examined in mixed aqueous/organic media (10, 25 and 50 vol% in organic solvent). After 3 h of UVC irradiation (50 vol% mixed media) defluorination with Ga2O3/N2 was ∼65% greater than in aqueous media, and ca. 80% greater than the direct photolysis of Fipronil under inert (N2) conditions; under air-equilibrated conditions both Ga2O3-photocatalyzed and photochemical defluorination were significantly lower than in aqueous media. Dechlorination of Fipronil was ∼160% (Ga2O3/N2) and 140% (photochemically, N2) greater than in aqueous media; under air-equilibrated conditions, both photocatalyzed and photochemical formation of Cl(-) ions in mixed media fell rather short relative to aqueous media. The photocatalyzed (Ga2O3/N2) and photochemical (N2) conversion of the sulfur group in Fipronil to SO4(2(-)) ions was ca. 20% and 30% greater, respectively, in mixed media, while under air-equilibrated conditions photocatalyzed desulfonation was nearly twofold less than in the aqueous phase; direct photolysis showed little variations in mixed media. Denitridation of the nitrogens in Fipronil occurred mostly through the formation of ammonia (as NH4(+)) under all conditions with negligible quantities of NO3(-); again mixed media

Investigation of SiO{sub 2}:Na{sub 2}O ratio as a corrosion inhibitor for metal alloys

Energy Technology Data Exchange (ETDEWEB)

Mohamad, N.; Othman, N. K. [School of Applied Physics, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 UKM Bangi, Selangor Darul Ehsan (Malaysia); Jalar, A. [Institute of Micro Engineering and Nanoelectronics (IMEN), Universiti Kebangsaan Malaysia, 43600 UKM Bangi, Selangor Darul Ehsan (Malaysia)

2013-11-27

The silicate is one of the potential compounds used as a corrosion inhibitor for metal alloys. The mixture between silica and sodium hydroxide (NaOH) succeeded to produce the silicate product. The formulation of a silicate product normally variable depended by the different ratio of SiO{sub 2}:Na{sub 2}O. This research utilized the agriculture waste product of paddy using its rice husk. In this study, the amorphous silica content in rice husk ash was used after rice husk burnt in a muffle furnace at a certain temperature. The X-ray diffraction (XRD) analysis was done to determine the existence of amorphous phase of silica in the rice husk ash. There are several studies that recognized rice husk as an alternative source that obtained high silica content. The X-ray fluorescence (XRF) analysis was carried out to clarify the percentage amount of Si and O elements, which referred the silica compound in rice husk ash. The preparation of sodium silicate formulation were differ based on the SiO{sub 2}:Na{sub 2}O ratio (SiO{sub 2}:Na{sub 2}O ratio = 1.00, 2.00 and 3.00). These silicate based corrosion inhibitors were tested on several testing samples, which were copper (99.9%), aluminum alloy (AA 6061) and carbon steel (SAE 1045). The purpose of this study is to determine the appropriate SiO{sub 2}:Na{sub 2}O ratio and understand how this SiO{sub 2}:Na{sub 2}O ratio can affect the corrosion rate of each metal alloys immersed in acidic medium. In order to investigate this study, weight loss test was conducted in 0.5 M hydrochloric acid (HCl) for 24 hours at room temperature.

Quantitative Evidence for Lanthanide-Oxygen Orbital Mixing in CeO2, PrO2, and TbO2.

Science.gov (United States)

Minasian, Stefan G; Batista, Enrique R; Booth, Corwin H; Clark, David L; Keith, Jason M; Kozimor, Stosh A; Lukens, Wayne W; Martin, Richard L; Shuh, David K; Stieber, S Chantal E; Tylisczcak, Tolek; Wen, Xiao-Dong

2017-12-13

Understanding the nature of covalent (band-like) vs ionic (atomic-like) electrons in metal oxides continues to be at the forefront of research in the physical sciences. In particular, the development of a coherent and quantitative model of bonding and electronic structure for the lanthanide dioxides, LnO 2 (Ln = Ce, Pr, and Tb), has remained a considerable challenge for both experiment and theory. Herein, relative changes in mixing between the O 2p orbitals and the Ln 4f and 5d orbitals in LnO 2 are evaluated quantitatively using O K-edge X-ray absorption spectroscopy (XAS) obtained with a scanning transmission X-ray microscope and density functional theory (DFT) calculations. For each LnO 2 , the results reveal significant amounts of Ln 5d and O 2p mixing in the orbitals of t 2g (σ-bonding) and e g (π-bonding) symmetry. The remarkable agreement between experiment and theory also shows that significant mixing with the O 2p orbitals occurs in a band derived from the 4f orbitals of a 2u symmetry (σ-bonding) for each compound. However, a large increase in orbital mixing is observed for PrO 2 that is ascribed to a unique interaction derived from the 4f orbitals of t 1u symmetry (σ- and π-bonding). O K-edge XAS and DFT results are compared with complementary L 3 -edge and M 5,4 -edge XAS measurements and configuration interaction calculations, which shows that each spectroscopic approach provides evidence for ground state O 2p and Ln 4f orbital mixing despite inducing very different core-hole potentials in the final state.

The puzzle of the CNO isotope ratios in asymptotic giant branch carbon stars

Science.gov (United States)

Abia, C.; Hedrosa, R. P.; Domínguez, I.; Straniero, O.

2017-03-01

Context. The abundance ratios of the main isotopes of carbon, nitrogen and oxygen are modified by the CNO-cycle in the stellar interiors. When the different dredge-up events mix the burning material with the envelope, valuable information on the nucleosynthesis and mixing processes can be extracted by measuring these isotope ratios. Aims: Previous determinations of the oxygen isotopic ratios in asymptotic giant branch (AGB) carbon stars were at odds with the existing theoretical predictions. We aim to redetermine the oxygen ratios in these stars using new spectral analysis tools and further develop discussions on the carbon and nitrogen isotopic ratios in order to elucidate this problem. Methods: Oxygen isotopic ratios were derived from spectra in the K-band in a sample of galactic AGB carbon stars of different spectral types and near solar metallicity. Synthetic spectra calculated in local thermodynamic equillibrium (LTE) with spherical carbon-rich atmosphere models and updated molecular line lists were used. The CNO isotope ratios derived in a homogeneous way, were compared with theoretical predictions for low-mass (1.5-3 M⊙) AGB stars computed with the FUNS code assuming extra mixing both during the RGB and AGB phases. Results: For most of the stars the 16O/17O/18O ratios derived are in good agreement with theoretical predictions confirming that, for AGB stars, are established using the values reached after the first dredge-up (FDU) according to the initial stellar mass. This fact, as far as the oxygen isotopic ratios are concerned, leaves little space for the operation of any extra mixing mechanism during the AGB phase. Nevertheless, for a few stars with large 16O/17O/18O, the operation of such a mechanism might be required, although their observed 12C/13C and 14N/15N ratios would be difficult to reconcile within this scenario. Furthermore, J-type stars tend to have lower 16O/17O ratios than the normal carbon stars, as already indicated in previous studies

Emergence of Griffiths phase and glassy mixed phase in Sm0.5Ca0.5MnO3 nanomanganites

International Nuclear Information System (INIS)

Giri, S.K.; Yusuf, S.M.; Mukadam, M.D.; Nath, T.K.

2014-01-01

Graphical abstract: A detailed investigation on the effect of grain size on formation of Griffiths phase, and glassy mixed phase in CE-type antiferromagnetic Sm 0.5 Ca 0.5 MnO 3 manganite are carried out. A rigorous measurement of linear and non-linear ac magnetic susceptibilities, time dependent relaxation and aging phenomena in Sm 0.5 Ca 0.5 MnO 3 nanomanganite confirm the existence of a glassy mixed phase in the low temperature regime. The signature of Griffiths phase in nanosized manganite has been confirmed from the detailed ac and dc magnetization studies. The existence of Griffiths phase is verified through the anomalous behavior of the low field temperature dependent an inverse ac and dc magnetic susceptibility. Based on experimental results, the glassy phase of nanomanganites has been attributed to the phase separation effect and interaction between the ferromagnetic clusters. A phenomenological core/shell model has also been proposed based on the surface disorder to explain the observed Griffiths phase in these nanosized manganites. Fig. 1: (Left) The plot of inverse of ac susceptibility χ ac -1 measured at f = 1 Hz and H ac = 2 Oe as a function of temperature for S750 sample. Inset shows the same for S550 sample. (Right) A schematic of the proposed model to describe the magnetic state of the Sm 0.5 Ca 0.5 MnO 3 system at different average sizes. Highlights: • Effect of grain size on Griffiths phase and glassy mixed phase is discussed. • GP is confirmed by dc, linear and non-linear ac magnetization in nanomanganites. • Glassy mixed phase is discussed by time dependent relaxation and aging phenomena. • The existence of GP is verified through an inverse ac and dc magnetic susceptibility. • A phenomenological core/shell model has been proposed based on surface disorder. -- Abstract: A detailed investigation on the effect of grain size on formation of Griffiths phase (GP), and glassy mixed phase in CE-type antiferromagnetic Sm 0.5 Ca 0.5 MnO 3

VizieR Online Data Catalog: C and O isotopic ratios in Arcturus and Aldebaran (Abia+ 2012)

Science.gov (United States)

Abia, C.; Palmerini, S.; Busso, M.; Cristallo, S.

2012-10-01

CNO abundances, C and O isotopic ratios and equivalent diffusive coefficients (D) are given for the calculated extra-mixing models. For Arcturus we used the electronic version of the Infrared Atlas Spectrum by Hinkle et al. (1995, Cat. J/PASP/107/1042; resolution 0.01cm-1), and for Aldebaran we used a spectrum obtained on February 6, 1980 at the KPNO 4m Coude telescope using a Fourier transform spectrometer, kindly provided by K. Hinkle (resolution 0.016cm-1) The first 2 rows of table4 report the CNO abundances and isotopic ratios resulting from the observations. The other rows give the CNO abundances and isotopic ratios accounted for by the FDU in the three stellar models considered of 1.3Mo, 1.2Mo and 1.08Mo (see the paper for more details). (1 data file).

Long-term O3–precursor relationships in Hong Kong: field observation and model simulation

Directory of Open Access Journals (Sweden)

Y. Wang

2017-09-01

Full Text Available Over the past 10 years (2005–2014, ground-level O3 in Hong Kong has consistently increased in all seasons except winter, despite the yearly reduction of its precursors, i.e. nitrogen oxides (NOx =  NO + NO2, total volatile organic compounds (TVOCs, and carbon monoxide (CO. To explain the contradictory phenomena, an observation-based box model (OBM coupled with CB05 mechanism was applied in order to understand the influence of both locally produced O3 and regional transport. The simulation of locally produced O3 showed an increasing trend in spring, a decreasing trend in autumn, and no changes in summer and winter. The O3 increase in spring was caused by the net effect of more rapid decrease in NO titration and unchanged TVOC reactivity despite decreased TVOC mixing ratios, while the decreased local O3 formation in autumn was mainly due to the reduction of aromatic VOC mixing ratios and the TVOC reactivity and much slower decrease in NO titration. However, the decreased in situ O3 formation in autumn was overridden by the regional contribution, resulting in elevated O3 observations. Furthermore, the OBM-derived relative incremental reactivity indicated that the O3 formation was VOC-limited in all seasons, and that the long-term O3 formation was more sensitive to VOCs and less to NOx and CO in the past 10 years. In addition, the OBM results found that the contributions of aromatics to O3 formation decreased in all seasons of these years, particularly in autumn, probably due to the effective control of solvent-related sources. In contrast, the contributions of alkenes increased, suggesting a continuing need to reduce traffic emissions. The findings provide updated information on photochemical pollution and its impact in Hong Kong.

Thermal behaviour of pure and binary Fe(NO3)3.9H2O and (NH4)6Mo7O24.4H2O systems

International Nuclear Information System (INIS)

Shaheen, W.M.

2007-01-01

Thermal behaviour of pure ferric nitrate, ammonium molybdate and their mixtures in different ratios were investigated by means of thermal analysis (TG, DTG and DTA) techniques. Relative thermal analysis (RTA) graphical treatment of derivatographic curves of the components in the pure and binary system has been carried out as well. A series of Fe 2 O 3 -MoO 3 systems were prepared from pure and binary salts by heating at 350, 550, 750 and 1000 deg. C. The X-ray diffraction (XRD) analysis was used to characterize the phases produced from thermal treatment of investigated solids. The results revealed that pure ferric nitrate decomposed to Fe 2 O 3 at 250, while pure ammonium molybdate decomposed into MoO 3 and 340 deg. C and then melted at 790 deg. C. For the binary components, crystalline ferric or molybdenum oxides were detected beside ferric molybdate Fe 2 (MoO 4 ) 3 phase starting from 350 deg. C. Fe 2 (MoO 4 ) 3 phase was formed as a result of solid-solid interactions between the produced oxides. The thermal stability of the formed compound was significantly affected by the composition of the mixture and treatment temperature. The presence of two-component solids in the binary systems affected the thermal decomposition of their individual salt and affected their physical and chemical behaviour. The catalytic activity of the obtained pure and mixed oxides was measured using the decomposition of hydrogen peroxide reaction as a model reaction at 20-50 deg. C. It was found that the mixed oxide solids had catalytic activity higher than single oxides thermally treated at 350 and 550 deg. C. This is attributed to the increase in the concentration of active sites via creation of new ion pairs in case of binary systems. The rise in calcination temperature up to 750 and 1000 deg. C brought about drastic decrease in the activity of all solids because of changing catalyst composition and/or sintering process. The activation energies of H 2 O 2 decomposition were determined

High resistance ratio of bipolar resistive switching in a multiferroic/high-K Bi(Fe0.95Cr0.05)O3/ZrO2/Pt heterostructure

Science.gov (United States)

Dong, B. W.; Miao, Jun; Han, J. Z.; Shao, F.; Yuan, J.; Meng, K. K.; Wu, Y.; Xu, X. G.; Jiang, Y.

2018-03-01

An novel heterostructure composed of multiferroic Bi(Fe0.95Cr0.05)O3 (BFCO) and high-K ZrO2 (ZO) layers is investigated. Ferroelectric and electrical properties of the BFZO/ZO heterostructure have been investigated. A pronounced bipolar ferroelectric resistive switching characteristic was achieved in the heterostructure at room temperature. Interestingly, the BFCO/ZO structures exhibit a reproducible resistive switching with a high On/Off resistance ratio ∼2×103 and long retention time. The relationship between polarization and band structure at the interface of BFCO/ZO bilayer under the positive and negative sweepings has been discussed. As a result, the BFCO/ZO multiferroic/high-K heterostructure with high On/Off resistance ratio and long retention characterizes, exhibits a potential in future nonvolatile memory application.

E2,M1 multipole mixing ratios in even-even nuclei, 58< or =A< or =150

International Nuclear Information System (INIS)

Krane, K.S.

1977-01-01

A survey is presented of E2,M1 multipole mixing ratios of gamma-ray transitions in even-even nuclei in the mass range 58< or =A< or =150. Angular distribution and correlation data from the literature are analyzed in terms of a consistent choice of the phase relationship between the E2 and M1 matrix elements. A set of recommended values of the mixing ratios is included based on averages of results from various studies. The survey includes data available in the literature up to December 1976

A medium range order structural connection to the configurational heat capacity of borate-silicate mixed glasses.

Science.gov (United States)

Liu, Hao; Smedskjaer, Morten M; Tao, Haizheng; Jensen, Lars R; Zhao, Xiujian; Yue, Yuanzheng

2016-04-28

It has been reported that the configurational heat capacity (C(p,conf)) first increases and then becomes saturated with increasing B2O3/SiO2 ratio in borate-silicate mixed glasses. Through Raman spectroscopy measurements, we have, in this work, found an implication for the intermediate range order (IRO) structural connection to the composition dependence of the C(p,conf) of borate-silicate mixed glasses. In the silica-rich compositions, the C(p,conf) rapidly increases with increasing B2O3 content. This is attributed to the increase of the content of the B-O-Si network units ([B2Si2O8](2-)) and 6-membered borate rings with 1 or 2 B(4). In the boron-rich compositions, the C(p,conf) is almost constant, independent of the increase in the B2O3/SiO2 ratio. This is likely attributed to the counteraction between the decrease of the fraction of two types of metaborate groups and the increase of the fraction of other borate superstructural units (particularly 6-membered borate rings). The overall results suggest that the glasses containing more types of superstructural units have a larger C(p,conf).

A new method for the determination of the mixing ratio hydrogen to helium in the giant planets.

Science.gov (United States)

Gautier, D.; Grossman, K.

1972-01-01

By using a numerical iterative method, it is demonstrated that the mixing ratio H2/He on the giant planets can be inferred from spectral measurements of the intensity emitted by these planets in the far infrared range. The method is successfully applied to synthetic spectra of Saturn computed from atmospheric thermal models. The effect of random and systematic measurement errors on the determination of the mixing ratio is also studied.

Transesterification of Jatropha curcas crude oil to biodiesel on calcium lanthanum mixed oxide catalyst: Effect of stoichiometric composition

International Nuclear Information System (INIS)

Taufiq-Yap, Yun Hin; Teo, Siow Hwa; Rashid, Umer; Islam, Aminul; Hussien, Mohd Zobir; Lee, Keat Teong

2014-01-01

Highlights: • Biodiesel synthesis from Jatropha curcas oil catalyzed by CaO–La 2 O 3 mixed oxide. • Effects of Ca-to-La ratio, catalyst concentration, methanol/oil ratio and reaction temperature were optimized. • Biodiesel yield >85% was achieved at 65 °C temperature. • CaO–La 2 O 3 catalyst can be easy regenerated. - Abstract: Heterogeneous solid mixed oxide (CaO–La 2 O 3 ) catalysts with different molar ratios of calcium to lanthanum (Ca-to-La) were synthesized by co-precipitation method. The synthesized solid CaO–La 2 O 3 mixed metal oxide catalysts were utilized in transesterification of Jatropha curcus oil as feedstock to produce biodiesel. Under the optimized conditions at 65 °C, 4% catalyst dose with 24:1 MeOH to Jatropha oil molar ratio, the transesterification reaction exhibited 86.51% of biodiesel yield. The prepared catalysts were characterized using various techniques such as X-ray diffraction (XRD), nitrogen sorption with Brunauer–Emmer–Teller (BET) method, temperature-programmed desorption of CO 2 (CO 2 -TPD) and scanning electron microscopy (SEM). Influence of Ca-to-La atomic ratio in the mixed metal oxide catalyst, catalyst amount, methanol to oil molar ratio, reaction time, different oils on the fatty acid methyl ester (FAME) yield were appraised. Different catalyst regeneration procedures were also performed to investigate the reusability of the CaO–La 2 O 3 catalyst

On the graphical extraction of multipole mixing ratios of nuclear transitions

International Nuclear Information System (INIS)

Rezynkina, K.; Lopez-Martens, A.; Hauschild, K.

2017-01-01

We propose a novel graphical method for determining the mixing ratios δ and their associated uncertainties for mixed nuclear transitions. It incorporates the uncertainties on both the measured and the theoretical conversion coefficients. The accuracy of the method has been studied by deriving the corresponding probability density function. The domains of applicability of the method are carefully defined.

On the graphical extraction of multipole mixing ratios of nuclear transitions

Energy Technology Data Exchange (ETDEWEB)

Rezynkina, K., E-mail: kseniia.rezynkina@csnsm.in2p3.fr; Lopez-Martens, A.; Hauschild, K.

2017-02-01

We propose a novel graphical method for determining the mixing ratios δ and their associated uncertainties for mixed nuclear transitions. It incorporates the uncertainties on both the measured and the theoretical conversion coefficients. The accuracy of the method has been studied by deriving the corresponding probability density function. The domains of applicability of the method are carefully defined.

Dielectric relaxation of selenium-tellurium mixed former glasses

Science.gov (United States)

Palui, A.; Ghosh, A.

2017-05-01

We report the study of dielectric properties of mixed network former glasses of composition 0.3Ag2O-0.7(xSeO2-(1-x)TeO2); x=0, 0.1, 0.3, 0.4, 0.5 and 0.6 in a wide frequency 10 Hz - 2 MHz and temperature range 223 K - 403 K. The experimental data have been analyzed in the framework of complex dielectric permittivity. The dielectric permittivity data have been analyzed using the Cole-Cole function. The inverse temperature dependence of relaxation time obtained from real part of dielectric permittivity data follows the Arrhenius relation. The activation energy shows mixed glass former effect with variation of mixed former ratio. A non-zero value of shape parameters is observed and it is almost independent of temperature and composition.

Synthesis of High Crystalline Al-Doped ZnO Nanopowders from Al2O3 and ZnO by Radio-Frequency Thermal Plasma

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Min-Kyeong Song

2015-01-01

Full Text Available High crystalline Al-doped ZnO (AZO nanopowders were prepared by in-flight treatment of ZnO and Al2O3 in Radio-Frequency (RF thermal plasma. Micron-sized (~1 μm ZnO and Al2O3 powders were mixed at Al/Zn ratios of 3.3 and 6.7 at.% and then injected into the RF thermal plasma torch along the centerline at a feeding rate of 6.6 g/min. The RF thermal plasma torch system was operated at the plate power level of ~140 kVA to evaporate the mixture oxides and the resultant vapor species were condensed into solid particles by the high flow rate of quenching gas (~7000 slpm. The FE-SEM images of the as-treated powders showed that the multipod shaped and the whisker type nanoparticles were mainly synthesized. In addition, these nanocrystalline structures were confirmed as the single phase AZO nanopowders with the hexagonal wurtzite ZnO structure by the XRD patterns and FE-TEM results with the SAED image. However, the composition changes of 0.3 and 1.0 at.% were checked for the as-synthesized AZO nanopowders at Al/Zn ratios of 3.3 and 6.7 at.%, respectively, by the XRF data, which can require the adjustment of Al/Zn in the mixture precursors for the applications of high Al doping concentrations.

Enhancement of oxidative electrocatalytic properties of platinum nanoparticles by supporting onto mixed WO{sub 3}/ZrO{sub 2} matrix

Energy Technology Data Exchange (ETDEWEB)

Rutkowska, Iwona A., E-mail: ilinek@chem.uw.edu.pl; Wadas, Anna; Kulesza, Pawel J., E-mail: pkulesza@chem.uw.edu.pl

2016-12-01

Highlights: • The electrocatalytic system utilizing Pt nanoparticles dispersed on mixed metal oxide (WO{sub 3}/ZrO{sub 2}) system is proposed. • The system is characterized by high activity toward oxidations of ethanol, methanol and acetaldehyde in acid medium. • The enhancement effect is facilitated by presence of hydroxyl groups, high mobility of protons and improved distribution of electrons. • Strong interactions between Pt and the mixed oxide WO{sub 3}/ZrO{sub 2} support are postulated. - Abstract: Nanostructured mixed metal (W, Zr) oxide matrices (in a form of layered intercalated films of WO{sub 3} and ZrO{sub 2}) are considered here for supporting and activating catalytic platinum nanoparticles toward electrooxidation of ethanol. Remarkable increases of electrocatalytic (voltammetric, chronoamperometric) currents measured in 0.5 mol dm{sup −3} H{sub 2}SO{sub 4} (containing 0.5 mol dm{sup −3} ethanol) have been observed. Comparison has been made to the behavior of methanol and acetaldehyde under analogous conditions. The enhancement effects are interpreted in terms of specific interactions between platinum nanoparticles and the metal oxide species, high acidity of the mixed oxide sites, as well as high population of surface hydroxyl groups and high mobility of protons existing in close vicinity of Pt catalytic sites. The metal oxide nanostructures are expected to interact competitively (via the surface hydroxyl groups) with adsorbates of the undesirable reaction intermediates, including CO, facilitating their desorption (“third body effect”), or even oxidative removal (e.g., of CO to CO{sub 2}). The fact that the partially reduced tungsten oxide (H{sub x}WO{sub 3}) component is characterized by fast electron transfers coupled to proton displacements tends to improve the overall charge propagation at the electrocatalytic interface.

Bending strength of glass-ceramics based on 3CaO.P{sub 2}O{sub 5}-SiO{sub 2}-MgO glass system; Resistencia a fratura de vitroceramicos do sistema 3CaO.P{sub 2}O{sub 5}-SiO{sub 2}-MgO

Energy Technology Data Exchange (ETDEWEB)

Daguano, J.K.M.F.; Suzuki, P.A.; Santos, C. [Universidade de Sao Paulo (EEL/USP), Lorena, SP (Brazil). Escola de Engenharia de Lorena. Dept. de Engenharia de Materiais; Fernandes, M.H.V. [Universidade de Aveiro (UAveiro/CECICO), Aveiro (Portugal). Centro de Investigacao em Materiais Ceramicos e Compositos. Dept. de Engenharia Ceramica e do Vidro; Elias, C.N. [Instituto Militar de Engenharia (IME), Rio de Janeiro, RJ (Brazil). Lab. de Biomateriais

2009-07-01

In this work, the Modulus of Rupture of bioactive glass-ceramic based on 3CaO.P{sub 2}O{sub 5}-SiO{sub 2}-MgO system was investigated, aiming its use in bone-restorations. The mechanical property was correlated with microstructural and crystallographic features of this material. High-purity starting-powders, CaCO{sub 3}, SiO{sub 2}, MgO, Ca (H{sub 2}PO{sub 4}).H{sub 2}O, were used in this study. The powders were mixed in a stoichiometric ratio, using planetary ball-mill. The suspensions were dried, sieved and melted at 1600 deg C, for 4h. The casting ones were cooled quickly until annealing temperature 700 deg C, in which remained for 2h, with controlled cooling-rate until ambient temperature. Bulks of glass were heat-treated with temperatures varying between 700 deg C and 1100 deg C, for 4h, being after that, cooled at 3 deg C/min. Bioactive glass and glass-ceramic were characterized by HRXRD (high resolution X-ray diffraction), where whitlockite was main phase. The microstructure was analyzed by scanning electronic microscopy. Modulus of Rupture was determined by four-point bending testing using specimens of 1.5 x 2 x 25 mm and glasses presented strength near to 70MPa, while glass ceramics treated at 975 deg C-4h, presented bending strength of 120MPa. (author)

Structure and crystallization of B{sub 2}O{sub 3}-Al{sub 2}O{sub 3}-SiO{sub 2} glasses

Energy Technology Data Exchange (ETDEWEB)

Cheng Yin, E-mail: zjbcy@126.co [College of Physics and Electronic Science, Changsha University of Science and Technology, Changsha 410114 (China); Xiao Hanning [College of Physics and Electronic Science, Changsha University of Science and Technology, Changsha 410114 (China); College of Materials Science and Engineering, Hunan University, Changsha 410082 (China); Shuguang Chen; Tang Bingzhong [College of Physics and Electronic Science, Changsha University of Science and Technology, Changsha 410114 (China)

2009-05-01

B{sub 2}O{sub 3}-Al{sub 2}O{sub 3}-SiO{sub 2} glasses with different B{sub 2}O{sub 3}/Al{sub 2}O{sub 3} ratios of 0.4-1.3 were prepared by the melting-quenching method at 1500-1600 deg. C for 2 h. Fragility index F was used to estimate the glass-forming ability. The infrared (IR) absorption curves and differential scanning calorimetry (DSC) curves of the glasses have been investigated for estimating the influence of the B{sub 2}O{sub 3}/Al{sub 2}O{sub 3} ratio on glass structure and crystallization of the B{sub 2}O{sub 3}-Al{sub 2}O{sub 3}-SiO{sub 2} glass system. The crystallization kinetics of the glasses were described by activation energy (E) for crystallization and calculated by the Kissinger method. X-ray diffraction (XRD) and SEM analyses were also used to describe the types and morphologies of the crystals precipitated from the B{sub 2}O{sub 3}-Al{sub 2}O{sub 3}-SiO{sub 2} glasses. The results show that with the increase of B{sub 2}O{sub 3}/Al{sub 2}O{sub 3} ratio, glass stability improves and the trend of crystallization decreases relatively. However, when the B{sub 2}O{sub 3}/Al{sub 2}O{sub 3} ratio reaches 1.3, boron-abnormal phenomenon appears and results in the raising trend of crystallization. Rod-like crystals of Al{sub 4}B{sub 2}O{sub 9} and Al{sub 20}B{sub 4}O{sub 36} were observed in the crystallized samples.

Óxidos Mistos de Al2O3/ZrO2 como Inibidores de Corrosão do Aço SAE 1020

Directory of Open Access Journals (Sweden)

Marcelo Rodrigues da Silva

2014-01-01

Full Text Available This paper describes the use of Al2O3/ZrO2 mixed oxides synthesized by sol-gel process with different amounts of ZrO2 (5%, 10%, 15% and 20% by mass in the Al2O3 matrix and different temperatures of calcination, such as interesting inhibitor materials of corrosive processes of SAE 1020 steel. The materials were characterized by Infrared Spectroscopy Fourier Transform (FTIR and X-Ray Diffraction (XRD techniques. FTIR spectra show the typical Al-O and Zr-O bonds vibrations in the mixed oxides. The XRD patterns of the samples calcined at 800 °C and 1000 °C shows the ZrO2 tetragonal and γ-Al2O3 face-centered cubic (FCC phases. The corrosion tests showed that the SAE 1020 steel covered with mixed oxides have an anodic passive region, thereby inhibiting the corrosive processes on the metal surface. Furthermore, the found values for steel coated with mixed oxide synthesized indicate a decrease in corrosion potentials (Ecor and corrosion current (icor. With respect to different samples of mixed oxides, the sample with 20 % of ZrO2 in the Al2O3 matrix proved to be the best inhibitor of steel corrosion, with the lowest values of corrosion potential and corrosion current, - 1.32 V and 0.31 μA cm-2, respectively.

The effect of CaO/SiO2 molar ratio of CaO-Al2O3-SiO2 glasses on their structure and reactivity in alkali activated system.

Science.gov (United States)

Kucharczyk, Sylwia; Sitarz, Maciej; Zajac, Maciej; Deja, Jan

2018-04-05

The influence of CaO/SiO 2 molar ratio of calcium aluminosilicate glasses on resulting structure and reactivity was investigated. Chemical compositions of glasses were chosen to mimic the composition of the fly ash and slag amorphous phase. Understanding the reactivity of these materials is of high importance allowing further development of the composite cements to limit the environmental footprint of cement industry. Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy were employed to examine the structure of glasses. Reactivity of the glasses was analyzed on paste samples after 1, 2, 7, 28 and 90days of curing by means of thermogravimetry (TGA), X-ray diffraction (XRD) and FTIR. Spectroscopic results emphasize dependence of the structure on the chemical composition of the glasses. The higher CaO/SiO 2 the more depolymerized the glass network is, though there is no direct correlation with the reactivity. Significant differences in reactivity is observed primarily between the glasses of peraluminous (CaO/Al 2 O 3 1). Amongst the pastes made of glasses of percalcic region a higher degree of reaction at later ages is observed for the paste containing glass of lower CaO/SiO 2 molar ratio. This is due to both degree of depolimerization and the nature of these glasses (pozzolanic and hydraulic materials). No difference of degree of reaction has been observed within the glasses of CaO/SiO 2 lower than 1. Copyright © 2018 Elsevier B.V. All rights reserved.

The effect of CaO/SiO2 molar ratio of CaO-Al2O3-SiO2 glasses on their structure and reactivity in alkali activated system

Science.gov (United States)

Kucharczyk, Sylwia; Sitarz, Maciej; Zajac, Maciej; Deja, Jan

2018-04-01

The influence of CaO/SiO2 molar ratio of calcium aluminosilicate glasses on resulting structure and reactivity was investigated. Chemical compositions of glasses were chosen to mimic the composition of the fly ash and slag amorphous phase. Understanding the reactivity of these materials is of high importance allowing further development of the composite cements to limit the environmental footprint of cement industry. Fourier transform infrared spectroscopy (FTIR) and Raman spectroscopy were employed to examine the structure of glasses. Reactivity of the glasses was analyzed on paste samples after 1, 2, 7, 28 and 90 days of curing by means of thermogravimetry (TGA), X-ray diffraction (XRD) and FTIR. Spectroscopic results emphasize dependence of the structure on the chemical composition of the glasses. The higher CaO/SiO2 the more depolymerized the glass network is, though there is no direct correlation with the reactivity. Significant differences in reactivity is observed primarily between the glasses of peraluminous (CaO/Al2O3 1). Amongst the pastes made of glasses of percalcic region a higher degree of reaction at later ages is observed for the paste containing glass of lower CaO/SiO2 molar ratio. This is due to both degree of depolimerization and the nature of these glasses (pozzolanic and hydraulic materials). No difference of degree of reaction has been observed within the glasses of CaO/SiO2 lower than 1.

Probability distribution functions of δ15N and δ18O in groundwater nitrate to probabilistically solve complex mixing scenarios

Science.gov (United States)

Chrystal, A.; Heikoop, J. M.; Davis, P.; Syme, J.; Hagerty, S.; Perkins, G.; Larson, T. E.; Longmire, P.; Fessenden, J. E.

2010-12-01

Elevated nitrate (NO3-) concentrations in drinking water pose a health risk to the public. The dual stable isotopic signatures of δ15N and δ18O in NO3- in surface- and groundwater are often used to identify and distinguish among sources of NO3- (e.g., sewage, fertilizer, atmospheric deposition). In oxic groundwaters where no denitrification is occurring, direct calculations of mixing fractions using a mass balance approach can be performed if three or fewer sources of NO3- are present, and if the stable isotope ratios of the source terms are defined. There are several limitations to this approach. First, direct calculations of mixing fractions are not possible when four or more NO3- sources may be present. Simple mixing calculations also rely upon treating source isotopic compositions as a single value; however these sources themselves exhibit ranges in stable isotope ratios. More information can be gained by using a probabilistic approach to account for the range and distribution of stable isotope ratios in each source. Fitting probability density functions (PDFs) to the isotopic compositions for each source term reveals that some values within a given isotopic range are more likely to occur than others. We compiled a data set of dual isotopes in NO3- sources by combining our measurements with data collected through extensive literature review. We fit each source term with a PDF, and show a new method to probabilistically solve multiple component mixing scenarios with source isotopic composition uncertainty. This method is based on a modified use of a tri-linear diagram. First, source term PDFs are sampled numerous times using a variation of stratified random sampling, Latin Hypercube Sampling. For each set of sampled source isotopic compositions, a reference point is generated close to the measured groundwater sample isotopic composition. This point is used as a vertex to form all possible triangles between all pairs of sampled source isotopic compositions

The effect of diameter ratio between transducers and reactor in sonication-assisted synthesis of Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Manaf, A., E-mail: azwar@ui.ac.id; Fahmi, Agam Aidil [Department of Physics, FMIPA, Universitas Indonesia, Kampus UI Depok (Indonesia); Yustanti, Erlina [Department of Physics, FMIPA, Universitas Indonesia, Kampus UI Depok (Indonesia); Department of Metallurgy, Faculty of Engineering, University of Sultan AgengTirtayasa Jl. Jenderal Sudirman KM 03 Cilegon-Banten 65134 (Indonesia)

2016-04-19

This paper describes the particle size characterization of mechanically alloyed Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} prepared with the aid of a high-power ultrasonic destruction. Analytical-grade BaCO{sub 3}, TiO{sub 2} and SrCO{sub 3} with a purity greater than 99 wt.% were used as precursors for Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3}. The mechanically powders were respectively sintered at 1200 °C for 3 hours to form crystalline powders. This work is aimed at studying the effect of diameter ratio between reactor and transducer of a high power sonicator on the Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} nanoparticles formation. The presence of a single phase of the two materials was confirmed by X-Ray Diffraction (XRD). The concentration of the particles in demineralized water was 3.0 g / 100 mL which become the object of 3 hours ultrasonic destruction subjected to the application of transducer in which the ratio between the diameter of the reactor and the transducer (D/d) was fixed at 1.4, 1.6 and 1.8 respectively. It was found that the mean particle size before the ultrasonic destruction was 538 nm for Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and 480 nm for Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3}. With D/d of 1.8, the mean particle size of the two materials was found to decrease drastically to 38 nm and 24 nm, respectively. These mean particle sizes were respectively comparable with that of the crystallite size of the particles derived using the Whole Powder Pattern Modelling (WPPM) from which the mean crystallite size of 22 nm for Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and 14 nm for Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} were obtained. It is then confirmed single nanocrystallite Ba{sub 0.7}Sr{sub 0.3}TiO{sub 3} and Ba{sub 0.3}Sr{sub 0.7}TiO{sub 3} particles were already achieved. We can conclude that the ultrasonic destruction to mechanically milled crystalline particles would be one

Photocatalytic decomposition of N2O over TiO2/g-C3N4 photocatalysts heterojunction

Science.gov (United States)

Kočí, K.; Reli, M.; Troppová, I.; Šihor, M.; Kupková, J.; Kustrowski, P.; Praus, P.

2017-02-01

TiO2/g-C3N4 photocatalysts with the various TiO2/g-C3N4 weight ratios from 1:2 to 1:6 were fabricated by mechanical mixing in water suspension followed by calcination. Pure TiO2 was prepared by thermal hydrolysis and pure g-C3N4 was prepared from commercial melamine by thermal annealing at 620 °C. All the nanocomposites were characterized by X-ray powder diffraction, UV-vis diffuse reflectance spectroscopy, Raman spectroscopy, infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, photoelectrochemical measurements and nitrogen physisorption. The prepared mixtures along with pure TiO2 and g-C3N4 were tested for the photocatalytic decomposition of nitrous oxide under UVC (λ = 254 nm), UVA (λ = 365 nm) and Vis (λ > 400 nm) irradiation. The TiO2/g-C3N4 nanocomposites showed moderate improvement compared to pure g-C3N4 but pure TiO2 proved to be a better photocatalyst under UVC irradiation. However, under UVA irradiation conditions, the photocatalytic activity of TiO2/g-C3N4 (1:2) nanocomposite exhibited an increase compared to pure TiO2. Nevertheless, further increase of g-C3N4 amount leads/led to a decrease in reactivity. These results are suggesting the nanocomposite with the optimal weight ratio of TiO2 and g-C3N4 have shifted absorption edge energy towards longer wavelengths and decreased the recombination rate of charge carriers compared to pure g-C3N4. This is probably due to the generation of heterojunction on the TiO2/g-C3N4 interface.

Morphological Control of Mesoporosity and Nanoparticles within Co3O4-CuO Electrospun Nanofibers: Quantum Confinement and Visible Light Photocatalysis Performance.

Science.gov (United States)

Pradhan, Amaresh C; Uyar, Tamer

2017-10-18

The one-dimensional (1D) mesoporous and interconnected nanoparticles (NPs) enriched composite Co 3 O 4 -CuO nanofibers (NFs) in the ratio Co:Cu = 1/4 (Co 3 O 4 -CuO NFs) composite have been synthesized by electrospinning and calcination of mixed polymeric template. Not merely the mesoporous composite Co 3 O 4 -CuO NFs but also single mesoporous Co 3 O 4 NFs and CuO NFs have been produced for comparison. The choice of mixed polymer templates such as polyvinylpyrrolidone (PVP) and polyethylene glycol (PEG) for electrospinning is responsible for the formation of 1D mesoporous NFs. The HR-TEM result showed evolution of interconnected nanoparticles (NPs) and creation of mesoporosity in all electrospun NFs. The quantum confinement is due to NPs within NFs and has been proved by the surface-enhanced Raman scattering (SERS) study and the UV-vis-NRI diffuse reflectance spectra (DRS). The high intense photoluminescence (PL) spectra showing blue shift of all NFs also confirmed the quantum confinement phenomena. The lowering of PL spectrum after mixing of CuO in Co 3 O 4 nanofibers framework (Co 3 O 4 -CuO NFs) proved CuO as an efficient visible light response low cost cocatalyst/charge separator. The red shifting of the band gap in composite Co 3 O 4 -CuO NFs is due to the internal charge transfer between Co 2+ to Co 3+ and Cu 2+ , proved by UV-vis absorption spectroscopy. Creation of oxygen vacancies by mixing of CuO and Co 3 O 4 also prevents the electron-hole recombination and enhances the photocatalytic activity in composite Co 3 O 4 -CuO NFs. The photocurrent density, Mott-Schottky (MS), and electrochemical impedance spectroscopy (EIS) studies of all NFs favor the high photocatalytic performance. The mesoporous composite Co 3 O 4 -CuO NFs exhibits high photocatalytic activity toward phenolic compounds degradation as compared to the other two NFs (Co 3 O 4 NFs and CuO NFs). The kinetic study of phenolic compounds followed first order rate equation. The high photocatalytic

Characteristics of NaNO3-Promoted CdO as a Midtemperature CO2 Absorbent.

Science.gov (United States)

Kim, Kang-Yeong; Kwak, Jin-Su; An, Young-In; Oh, Kyung-Ryul; Kwon, Young-Uk

2017-06-28

In this study, we explored the reaction system CdO(s) + CO 2 (g) ⇄ CdCO 3 (s) as a model system for CO 2 capture agent in the intermediate temperature range of 300-400 °C. While pure CdO does not react with CO 2 at all up to 500 °C, CdO mixed with an appropriate amount of NaNO 3 (optimal molar ratio NaNO 3 /CdO = 0.14) greatly enhances the conversion of CdO into CdCO 3 up to ∼80% (5.68 mmol/g). These NaNO 3 -promoted CdO absorbents can undergo many cycles of absorption and desorption by temperature swing between 300 and 370 °C under a 100% CO 2 condition. Details of how NaNO 3 promotes the CO 2 absorption of CdO have been delineated through various techniques using thermogravimetry, coupled with X-ray diffraction and electron microscopy. On the basis of the observed data, we propose a mechanism of CO 2 absorption and desorption of NaNO 3 -promoted CdO. The absorption proceeds through a sequence of events of CO 2 adsorption on the CdO surface covered by NaNO 3 , dissolution of so-formed CdCO 3 , and precipitation of CdCO 3 particles in the NaNO 3 medium. The desorption occurs through the decomposition of CdCO 3 in the dissolved state in the NaNO 3 medium where CdO nanoparticles are formed dispersed in the NaNO 3 medium. The CdO nanoparticles are aggregated into micrometer-large particles with smooth surfaces and regular shapes.

Effects of dopant ion and Mn valence state in the La{sub 1-x}A{sub x}MnO{sub 3} (A=Sr,Ba) colossal magnetoresistance films

Energy Technology Data Exchange (ETDEWEB)

Choi, Sun Gyu; Wang, Seok-Joo; Park, Hyung-Ho; Hong, MunPyo; Kwon, Kwang-Ho [Department of Materials Science and Engineering, Yonsei University, 134 Sinchon-dong, Seodaemun-ku, Seoul 120-749 (Korea, Republic of); Department of Display and Semiconductor Physics, Korea University, Jochiwon, Chungnam 339-700 (Korea, Republic of); Department of Control and Instrumentation Engineering, Korea University, Jochiwon, Chungnam 339-700 (Korea, Republic of)

2010-01-15

The structural and electrical properties of Mn-based colossal magnetoresistance (CMR) thin films with controlled tolerance factor and Mn ion valance ratio were studied using crystal structure and chemical bonding character analyses. La{sub 0.7}Sr{sub 0.3}MnO{sub 3}, La{sub 0.7}Ba{sub 0.3}MnO{sub 3}, and La{sub 0.82}Ba{sub 0.18}MnO{sub 3} thin films with different contents of divalent cations and Mn{sup 3+}/Mn{sup 4+} ratios were deposited on amorphous SiO{sub 2}/Si substrate by rf magnetron sputtering at a substrate temperature of 350 deg. C. The films showed the same crystalline structure as the pseudocubic structure. The change in the sheet resistance of films was analyzed according to strain state of the unit cell, chemical bonding character of Mn-O, and Mn{sup 3+}/Mn{sup 4+} ratio controlling the Mn{sup 3+}-O{sup 2-}-Mn{sup 4+} conducting path. Mn L-edge x-ray absorption spectra revealed that the Mn{sup 3+}/Mn{sup 4+} ratio changed according to different compositions of Sr or Ba and the Mn 2p core level x-ray photoelectron spectra showed that the Mn 2p binding energy was affected by the covalence of the Mn-O bond and Mn{sup 3+}/Mn{sup 4+} ratio. In addition, O K-edge x-ray absorption spectra showed covalently mixed Mn 3d and O 2p states and matched well with the resistivity changes of CMR films. Temperature coefficient of resistance values were obtained at approximately -2.16%/K to -2.46%/K of the CMR films and were correct for infrared sensor applications.

Mixed ZnO-TiO2 Suspended Solution as an Efficient Photocatalyst for Decolonization of a Textile Dye from Waste Water

Directory of Open Access Journals (Sweden)

Mohammad Ali Mooji

2015-03-01

Full Text Available Introduction: Textile industries produce large volume of colored dye effluents which are toxic and removal of dyes from wastewater is a significant environmental issue. Advanced oxidation process (AOPs is alternative method for the complete degradation many organic pollutants. ZnO and TiO2 are important photocatalysts with high catalytic activity that have attracted much research attention. Material and Methods: Mixed ZnO/TiO2 was prepared with mixing of ZnO and TiO2 (20, 40, 60, 80 % (w/w. 20 mL of dye solution (80 mgL-1 for DB71 containing the appropriate quantity of photocatalyst was magnetically stirred under UV irradiation. Photocatalytic study was carried out to evaluate the effect of UV (400 W, ZnO/TiO2 weight percent (20, 40, 60, 80 % (w/w, pH (2.3 – 9.2, irradiation time of (10 – 70 min, initial dye concentration of (10, 40, 80 mg/L and ZnO/TiO2 dosage of (0.2 – 1.6 g/L on removal of dye. Dye concentration was monitored spectrophotometrically by measuring the dye absorbance at 285 nm. Results: In comparison with TiO2 or ZnO as photocatalyst, mixed photocatalyst (ZnO/TiO2 is more efficient catalyst for degradation of dye under UV irradiation Results show that approximately 90 % of Direct Blue 71 has been eliminated after 70 minutes and optimized condition ((pH = 6.4, ZnO/TiO2 (50% w/w, 1.25 g/L. Experiments showed, the noticeable decolorization of dye solution can be done without any oxidation agent with mixed ZnO/TiO2 photocatalyst.

Effect of Y2O3-Al2O3 ratio on inter-granular phases and films in tape-casting α-SiC with high toughness

International Nuclear Information System (INIS)

Huang Rong; Gu Hui; Zhang Jingxian; Jiang Dongliang

2005-01-01

Silicon carbide (SiC) ceramics prepared from liquid phase sintering after aqueous-tape-casting can yield high toughness when appropriate amount of Y 2 O 3 -Al 2 O 3 are added, even though no elongated grains are present. Grain boundaries (GB), second-phases and hetero-phase boundaries (HB) in 2 samples with additive mole ratios of 3:5 and 3:7 are investigated using high-resolution and analytical electron microscopy (HREM and AEM). The meta-stable YAlO 3 (YAP) was nucleated from SiC surfaces in the sample with Y/Al = 3:5 as revealed by crystallographic relations across the HB, whilst relatively thick amorphous films were found at GB. In contrary, the higher level of Al 2 O 3 additives decreases the GB film thickness in the sample with Y/Al = 3:7, and the homogeneous nucleation of Y 3 Al 5 O 12 (YAG) occurs at triple pockets accompanying with thick HB films. The strong variation of GB widths is a result of GB wetting in the sample with Y/Al = 3:5 and HB wetting in the sample of Y/Al = 3:7, both by liquid Al 2 O 3 . The energy of GB in the former sample is higher than the energy of HB as exhibited by the preferential nucleation of meta-stable YAP on SiC surfaces, which results in wetting of GB by the liquid; the situation is opposite in the latter sample as the wetting of HB occurs, leading to de-wetting of GB. The thermal mismatch between SiC and YAP or YAG as well as the presence of amorphous films facilitate the creation of micro-crack to promote inter-granular fracture and result in high toughness in both SiC ceramics

Changes in monoterpene mixing ratios during summer storms in rural New Hampshire (USA)

Science.gov (United States)

Haase, K.B.; Jordan, C.; Mentis, E.; Cottrell, L.; Mayne, H.R.; Talbot, R.; Sive, B.C.

2011-01-01

Monoterpenes are an important class of biogenic hydrocarbons that influence ambient air quality and are a principle source of secondary organic aerosol (SOA). Emitted from vegetation, monoterpenes are a product of photosynthesis and act as a response to a variety of environmental factors. Most parameterizations of monoterpene emissions are based on clear weather models that do not take into account episodic conditions that can drastically change production and release rates into the atmosphere. Here, the ongoing monoterpene dataset from the rural Thompson Farm measurement site in Durham, New Hampshire is examined in the context of a set of known severe storm events. While some storm systems had a negligible influence on ambient monoterpene mixing ratios, the average storm event increased mixing ratios by 0.59 ?? 0.21 ppbv, a factor of 93 % above pre-storm levels. In some events, mixing ratios reached the 10's of ppbv range and persisted overnight. These mixing ratios correspond to increases in the monoterpene emission rate, ranging from 120 to 1240 g km-2 h -1 compared to an estimated clear weather rate of 116 to 193 g km-2 h-1. Considering the regularity of storm events over most forested areas, this could be an important factor to consider when modeling global monoterpene emissions and their resulting influence on the formation of organic aerosols. ?? 2011 Author(s).

Properties of experimental titanium cast investment mixing with water reducing agent solution.

Science.gov (United States)

Zhang, Zutai; Ding, Ning; Tamaki, Yukimichi; Hotta, Yasuhiro; Han-Cheol, Cho; Miyazaki, Takashi

2012-01-01

This study aimed to develop a dental investment for titanium casting. ZrO(2) and Al(2)O(3) were selected as refractory materials to prepare three investments (Codes: A-C) according to the quantity of Zr. Al(2)O(3) cement was used as a binder at a ratio of 15%, they were mixed with special mixing liquid. B1 was used as a control mixed with water. Fundamental examinations were statistically evaluated. A casting test was performed with investment B. Fluidities, setting times, and green strengths showed no remarkable differences; however, they were significantly different from those of B1. Expansion values for A, B, C, and B1 at 850°C were 1.03%±0.08%, 1.96%±0.17%, 4.35%±0.23%, and 1.50%±0.28%, respectively. Castings were covered by only small amounts of mold materials. The hardness test showed no significant differences between castings from B and the ones from commercial investments. The experimental special mixing liquid effectively reduced the water/powder ratio and improved the strength and thermal expansion.

Engineering Mixed Ionic Electronic Conduction in La 0.8 Sr 0.2 MnO 3+ δ Nanostructures through Fast Grain Boundary Oxygen Diffusivity

KAUST Repository

Saranya, Aruppukottai M.; Pla, Dolors; Morata, Alex; Cavallaro, Andrea; Canales-Vá zquez, Jesú s; Kilner, John A.; Burriel, Mó nica; Tarancó n, Albert

2015-01-01

to implement in nanostructures. Here, an artificial mixed ionic electronic conducting oxide is fabricated by grain boundary (GB) engineering thin films of La0.8Sr0.2MnO3+δ. This electronic conductor is converted into a good mixed ionic electronic conductor

A Microdrop Generator for the Calibration of a Water Vapor Isotope Ratio Spectrometer

NARCIS (Netherlands)

Iannone, Rosario Q.; Romanini, Daniele; Kassi, Samir; Meijer, Harro A. J.; Kerstel, Erik R. Th.

A microdrop generator is described that produces water vapor with a known isotopic composition and volume mixing ratio for the calibration of a near-infrared diode laser water isotope ratio spectrometer. The spectrometer is designed to measure in situ the water vapor deuterium and oxygen ((17)O and

Steam reforming of ethanol over Co3O4–Fe2O3 mixed oxides

KAUST Repository

Abdelkader, A.; Daly, H.; Saih, Y.; Morgan, K.; Mohamed, M.A.; Halawy, S.A.; Hardacre, C.

2013-01-01

solvent/dispersing agent. The catalysts were studied in the steam reforming of ethanol to investigate the effect of the partial substitution of Co3O4 with Fe2O 3 on the catalytic behaviour. The reforming activity over Fe 2O3, while initially high

Net Community and Gross Photosynthetic Production Rates in the Eastern Tropical South Pacific, as Determined from O2/AR Ratios and Triple Oxygen Isotopic Composition of Dissolved O2

Science.gov (United States)

Prokopenko, M. G.; Yeung, L. Y.; Berelson, W.; Fleming, J.; Rollins, N.; Young, E. D.; Haskell, W. Z.; Hammond, D. E.; Capone, D. G.

2010-12-01

This study assesses the rates of ocean carbon production and its fate with respect to recycling or export in the Eastern Tropical South Pacific (ETSP). ETSP has been previously identified as a region where N2 fixation and denitrification may be spatially coupled; this is also a region of localized CO2 outgassing. Using an Equilibrated Inlet Mass Spectrometer (EIMS) system, we obtained continuous measurements of the biological O2 supersaturation in the mixed layer along the ship track encompassing a region bounded by 10-20° S and 80-100° W in January - March, 2010. Vertical profiles were also taken at selected stations and analyzed for dissolved O2/Ar ratios on EIMS and triple oxygen isotope composition (17O excess) on a multi-collector IRMS (Isotope Ratio Mass Spectrometer) at UCLA. Gas exchange rates were estimated using two approaches: the Rn-222 deficit method and the wind parameterization method, which utilized wind speeds extracted from ASCAT satellite database. Oxygen Net Community Production (O-NCP) rates calculated based on biological O2 supersaturation ranged from slightly negative to ~ 0.3 - 15 mmol/m2d, with higher rates along the northern part of the transect. Oxygen Gross Community Production (O-GPP) rates calculated from 17O excess were between 50 ± 20 and 200 ± 40 mmol/m2d, with higher rates observed along the northern cruise transect as well. Notably, the NCP/GPP ratios along the northern transect were higher by the factor of 2 to 3 than their southern counterparts. The O2/Ar-based NCP rates were comparable to POC flux measured with floating traps deployed at the southern stations, but exceeded by a factor of 5-10 the trap POC fluxes obtained at the northern stations. A one-dimensional box model has been constructed to quantify the magnitude of oxygen primary production below the mixed layer. The results of this work will be integrated with measurements of 15-N2 uptake that are in progress, to constrain the potential contribution of N2 fixation

Upconversion properties of Er3+/Yb3+ co-doped TeO2-TiO2-K2O glasses.

Science.gov (United States)

Su, Fangning; Deng, Zaide

2006-01-01

The Er3+/Yb3+ co-doped TeO2-TiO2-K2O glasses were prepared by conventional melting procedures, and their upconversion spectra were performed. The dependence of luminescence intensity on the ratio of Yb3+/Er3+ was studied, and the relationship between green upconversion luminescence intensity and Er3+ concentration is discussed in detail. The 546 nm green upconversion luminescence intensity is optimised in the studied glasses either when the Yb3+/Er3+ ratio is 25/1 and Er3+ concentration is 0.1 mol%, or when the Yb3+/Er3+ ratio is 10/1 and Er3+ concentration is 0.15 mol%. These glasses could be one of the potential candidates for LD pumping microchip solid-state lasers.

Film fabrication of Fe or Fe3O4 nanoparticles mixed with palmitic acid for vertically aligned carbon nanotube growth using Langmuir-Blodgett technique

Science.gov (United States)

Nakamura, Kentaro; Kuriyama, Naoki; Takagiwa, Shota; Sato, Taiga; Kushida, Masahito

2016-03-01

Vertically aligned carbon nanotubes (VA-CNTs) were studied as a new catalyst support for polymer electrolyte fuel cells (PEFCs). Controlling the number density and the diameter of VA-CNTs may be necessary to optimize PEFC performance. As the catalyst for CNT growth, we fabricated Fe or Fe3O4 nanoparticle (NP) films by the Langmuir-Blodgett (LB) technique. The catalyst Fe or Fe3O4 NPs were widely separated by mixing with filler molecules [palmitic acid (C16)]. The number density of VA-CNTs was controlled by varying the ratio of catalyst NPs to C16 filler molecules. The VA-CNTs were synthesized from the catalyst NP-C16 LB films by thermal chemical vapor deposition (CVD) using acetylene gas as the carbon source. The developing solvents used in the LB technique and the hydrogen reduction conditions of CVD were optimized to improve the VA-CNT growth rate. We demonstrate that the proposed method can independently control both the density and the diameter of VA-CNTs.

Winter- and summertime continental influences on tropospheric O3 and CO observed by TES over the western North Atlantic Ocean

Directory of Open Access Journals (Sweden)

R. Talbot

2010-04-01

Full Text Available The distributions of tropospheric ozone (O3 and carbon monoxide (CO, and the synoptic factors regulating these distributions over the western North Atlantic Ocean during winter and summer were investigated using profile retrievals from the Tropospheric Emission Spectrometer (TES for 2004–2006. Seasonal composites of TES retrievals, reprocessed to remove the influence of the a priori on geographical and seasonal structure, exhibited strong seasonal differences. At the 681 hPa level during winter months of December, January and February (DJF the composite O3 mixing ratios were uniformly low (~45 ppbv, but continental export was evident in a channel of enhanced CO (100–110 ppbv flowing eastward from the US coast. In summer months June, July, and August (JJA O3 mixing ratios were variable (45–65 ppbv and generally higher due to increased photochemical production. The summer distribution also featured a channel of enhanced CO (95–105 ppbv flowing northeastward around an anticyclone and exiting the continent over the Canadian Maritimes around 50° N. Offshore O3-CO slopes were generally 0.15–0.20 mol mol−1 in JJA, indicative of photochemical O3 production. Composites for 4 predominant synoptic patterns or map types in DJF suggested that export to the lower free troposphere (681 hPa level was enhanced by the warm conveyor belt airstream of mid-latitude cyclones while stratospheric intrusions increased TES O3 levels at 316 hPa. A major finding in the DJF data was that offshore 681 hPa CO mixing ratios behind cold fronts could be enhanced up to >150 ppbv likely by lofting from the surface via shallow convection resulting from rapid destabilization of cold air flowing over much warmer ocean waters. In JJA composites for 3 map types showed that the general export pattern of the seasonal composites was associated with a synoptic pattern featuring the Bermuda High. However, weak cyclones and frontal troughs could enhance offshore 681 hPa CO

Persistent low-temperature spin dynamics in the mixed-valence iridate Ba3InIr2O9

Science.gov (United States)

Dey, Tusharkanti; Majumder, M.; Orain, J. C.; Senyshyn, A.; Prinz-Zwick, M.; Bachus, S.; Tokiwa, Y.; Bert, F.; Khuntia, P.; Büttgen, N.; Tsirlin, A. A.; Gegenwart, P.

2017-11-01

Using thermodynamic measurements, neutron diffraction, nuclear magnetic resonance, and muon spin relaxation, we establish putative quantum spin-liquid behavior in Ba3InIr2O9 , where unpaired electrons are localized on mixed-valence Ir2O9 dimers with Ir4.5 + ions. Despite the antiferromagnetic Curie-Weiss temperature on the order of 10 K, neither long-range magnetic order nor spin freezing are observed down to at least 20 mK, such that spins are short-range correlated and dynamic over nearly three decades in temperature. Quadratic power-law behavior of both the spin-lattice relaxation rate and specific heat indicates the gapless nature of the ground state. We envisage that this exotic behavior may be related to an unprecedented combination of the triangular and buckled honeycomb geometries of nearest-neighbor exchange couplings in the mixed-valence setting.

Aircraft observations of aerosols O{sub 3} and NO{sub y} in a nighttime urban plume

Energy Technology Data Exchange (ETDEWEB)

Berkowitz, C.M.; Zaveri, R.A.; Xindi Bian; Shiyuan Zhong; Disselkamp, R.S.; Laulainen, N.S.; Chapman, E.G. [Pacific Northwest National Lab., Richland, WA (United States)

2001-05-01

Nighttime measurements of aerosol surface area, O{sub 3}, NO{sub y} and moisture were made downwind of Portland, Oregon, as part of a study to characterize the chemistry in a nocturnal urban plume. Air parcels sampled within the urban plume soon after sunset had positive correlations between O{sub 3}, relative humidity, NO{sub y} and aerosol number density. However, the air parcels sampled within the urban plume just before dawn had O{sub 3} mixing ratios that were highly anti-correlated with aerosol number density, NO{sub y} and relative humidity. Back-trajectories from a mesoscale model show that both the post-sunset and pre-dawn parcels came from a common maritime source to the northwest of Portland. The pre-dawn parcels with strong anti-correlations passed directly over Portland in contrast to the other parcels that were found to pass west of Portland. Several gas-phase mechanisms and a heterogeneous mechanism involving the loss of O{sub 3} to the aerosol surface, are examined to explain the observed depletion in O{sub 3} within the pre-dawn parcels that had passed over Portland. (Author)

Self-propagating high-temperature synthesis of Sr-doped LaMnO3 perovskite as oxidation catalyst

International Nuclear Information System (INIS)

Hirano, T.; Purwanto, H.; Watanabe, T.; Akiyama, T.

2007-01-01

Sr-doped LaMnO 3 perovskite oxide has been focused on as one of the alternative catalysts to precious metals such as platinum that are used for cleaning automotive emission gas. The conventional Solid-state reaction method is a popular productive process for perovskite oxide, however, it is time and energy consuming process because it requires repeated prolonged heat treatment at high temperatures. Therefore, the purposes of this work are to produce Sr-doped LaMnO 3 perovskite by using Self-propagating high-temperature synthesis (SHS) and experimentally examine the oxidation catalytic activity of the product for cleaning automotive emission gas. In the SHS, powders of La 2 O 3 , SrCO 3 , Mn and NaClO 4 were well mixed at the desired ratio and poured in a graphite crucible, where at one end it was ignited by using an electrically heated carbon foil. The wave of exothermic reaction due to oxidation of manganese propagated to the other end in a short time. The obtained products were characterized by means of XRD, FE-SEM, BET and particle size distribution analysis and then evaluated via catalytic oxidation tests by using propane in a fixed bed reactor at several temperatures. From the XRD analysis, the products had the desired composition of La 1-x Sr x MnO 3 (x = 0, 0.1, 0.2 and 0.4) perovskite, in which the replacing ratio x of La and Sr in the products was easily controlled by changing the mixing ratio of raw materials. The catalytic activity test showed that the samples exhibited good catalytic activity for propane oxidation over 200 deg. C , although the products had a relatively small surface area. SHS showed the potential for the production of a relatively inexpensive catalytic converter

Studies on the Ln/sub 2/O/sub 3/ (Ln: rare-earth elements)-SrO-V/sub 2/O/sub 3/ system, 1. Phase diagrams at 1400/sup 0/C

Energy Technology Data Exchange (ETDEWEB)

Shin-ike, T [Osaka Dental Coll., Hirakata (Japan); Adachi, G; Shiokawa, J

1980-11-01

Rare-earth oxides Ln/sub 2/O/sub 3/ (Ln : Nd, Eu or Er), strontium oxide SrO and vanadium oxide V/sub 2/O/sub 3/ were mixed in a given molecular ratio, heated at 1400/sup 0/C in vacuum. The products were examined by an x-ray diffraction method to study the phase relations of the ternary systems. On heating, part of the trivalent vanadium was oxidized to the tetravalent state by atmospheric oxygen. In this experimental condition, the following ternary-phase solid solutions were identified: perovskite type Nd sub(1-x)Sr sub(x)VO sub(3-0.1x) (x > 0.3. cubic, x < 0.3: orthorhombic) and Eu sub(1-x)Sr sub(x)VO sub(3-0.1x) (x > 0.4: cubic, x < 0.4: orthorhombic), K/sub 2/NiF/sub 4/ type SrO.Nd sub(1-x)Sr sub(x)VO sub(3-0.1x) (x > 0.3) and SrO.Eu sub(1-x)Sr sub(x)VO sub(3-0.1x) (x > 0.4) and Eu/sub 3/Ti/sub 2/O/sub 7/ type SrO.2Nd sub(1-x)Sr sub(x)VO sub(3-0.1x) (x > 0.3) and SrO.2Eu sub(1-x)Sr sub(x)VO sub(3-0.1x) (x > 0.4). For the Er/sub 2/O/sub 3/-SrO-V/sub 2/O/sub 3/ system, only a mixture of Er/sub 2/O/sub 3/, SrVO sub(2.9), ErVO/sub 3/, SrO and V/sub 2/O/sub 3/ was obtained.

Comparative Analysis of Alternative Spectral Bands of CO2 and O2 for the Sensing of CO2 Mixing Ratios

Science.gov (United States)

Pliutau, Denis; Prasad, Narasimha S.

2013-01-01

We performed comparative studies to establish favorable spectral regions and measurement wavelength combinations in alternative bands of CO2 and O2, for the sensing of CO2 mixing ratios (XCO2) in missions such as ASCENDS. The analysis employed several simulation approaches including separate layers calculations based on pre-analyzed atmospheric data from the modern-era retrospective analysis for research and applications (MERRA), and the line-byline radiative transfer model (LBLRTM) to obtain achievable accuracy estimates as a function of altitude and for the total path over an annual span of variations in atmospheric parameters. Separate layer error estimates also allowed investigation of the uncertainties in the weighting functions at varying altitudes and atmospheric conditions. The parameters influencing the measurement accuracy were analyzed independently and included temperature sensitivity, water vapor interferences, selection of favorable weighting functions, excitations wavelength stabilities and other factors. The results were used to identify favorable spectral regions and combinations of on / off line wavelengths leading to reductions in interferences and the improved total accuracy.

Mixing ratio and species affect the use of substrate-derived CO2 by Sphagnum

NARCIS (Netherlands)

Limpens, J.; Robroek, B.J.M.; Heijmans, M.M.P.D.; Tomassen, H.B.M.

2008-01-01

Question: Can mixing ratio and species affect the use of substrate-derived CO2 by Sphagnum? Location: Poor fen in south Sweden and greenhouse in Wageningen, The Netherlands. Methods: Two mixing ratios of Sphagnum cuspidatum and S. magellanicum were exposed to two levels of CO2 by pumping CO2

Physical and thermal behaviour of Sr-La-Al-B-Si based SOFC glass sealants as function of SrO content and B2O3/SiO2 ratio in the matrix

Science.gov (United States)

Ojha, Prasanta Kumar; Rath, S. K.; Chongdar, T. K.; Gokhale, N. M.; Kulkarni, A. R.

2011-05-01

A series of SOFC glass sealants with composition SrO (x), La2O3 (15), Al2O3 (15), B2O3 (40 - x), and SiO2 (30) [x = 10, 15, 20, 25 and 30] (wt.%) [SLABS] are investigated for their structure property correlations at different compositions. Quantitative Fourier transform infrared spectroscopy shows structural rigidity with increasing SrO content, as demonstrate by an increase in the Si-O-Si/O-Si-O bending and B-O-B stretching frequencies. The role of SrO as a modifier dominates the control of the structure and behaviour of glasses compared with the effect of network formers, i.e., the B2O3/SiO2 ratio. Consequent to the structural changes, increasing substitution of B2O3 by SrO the glasses causes increases in the density, glass transition temperature and dilatometric softening point. On the other hand, the crystallization temperatures show a decreasing trend and the coefficient of thermal expansion increases with increase in substitution.

Evaluations of absorbed dose ratio factor of Al2O3 dosemeter in radiotherapy photon beams using cavity theory

International Nuclear Information System (INIS)

Zhu, J.; Chen, S.; Chen, L.; Liu, X.

2012-01-01

The aim of the work was to evaluate the absorbed dose ratio factor f md of an Al 2 O 3 dosemeter to water in photon radiotherapy beams using cavity theory. Burlin theory was used for calculating of this ratio. The effective mass attenuation coefficient β was obtained by comparing Monte Carlo simulations in monoenergetic photon beams. The evaluations of the absorbed dose ratio factor f md were studied for Al 2 O 3 dosemeters of different sizes, which were placed at various depths of the water phantom in different radiation field sizes of Mohan's 6, 10 and 15-MV X-rays. Beyond the build-up region, the variation of f md increases by 0.25 % as the depth increases from 4 to 10 cm. The maximum variation due to different dosemeter sizes is 8.3 %. The difference in the f md due to different radiation field sizes is 1.5 %. The effect of the dosemeter size cannot be neglected. The difference in the f md due to the radiation field sizes of different beams would increase as the dosemeter size increases. (authors)

Changes in monoterpene mixing ratios during summer storms in rural New Hampshire (USA

Directory of Open Access Journals (Sweden)

K. B. Haase

2011-11-01

Full Text Available Monoterpenes are an important class of biogenic hydrocarbons that influence ambient air quality and are a principle source of secondary organic aerosol (SOA. Emitted from vegetation, monoterpenes are a product of photosynthesis and act as a response to a variety of environmental factors. Most parameterizations of monoterpene emissions are based on clear weather models that do not take into account episodic conditions that can drastically change production and release rates into the atmosphere. Here, the monoterpene dataset from the rural Thompson Farm measurement site in Durham, New Hampshire is examined in the context of a set of known severe storm events. While some storm systems had a negligible influence on ambient monoterpene mixing ratios, the average storm event increased mixing ratios by 0.59 ± 0.21 ppbv, a factor of 93% above pre-storm levels. In some events, mixing ratios reached the 10's of ppbv range and persisted overnight. These mixing ratios correspond to increases in the monoterpene emission rate, ranging from 120 to 1240 g km⁻² h⁻¹ compared to an estimated clear weather rate of 116 to 193 g km⁻² h⁻¹. Considering the regularity of storm events over most forested areas, this could be an important factor to consider when modeling global monoterpene emissions and their resulting influence on the formation of organic aerosols.

Phase diagram study for the PbO-ZnO-CaO-SiO_2 -“Fe_2O_3 ” system in air with CaO/SiO_2 in 1.1 and PbO/(CaO+SiO_2) in 2.4 weight ratios

International Nuclear Information System (INIS)

Lopez-Rodriguez, Josue; Romero-Serrano, Antonio; Hernandez-Ramirez, Aurelio; Cruz-Ramirez, Alejandro; Almaguer-Guzman, Isaias; Benavides-Perez, Ricardo; Flores-Favela, Manuel

2017-01-01

An experimental study on the phase equilibrium and the liquidus isotherms for the PbO-ZnO-CaO-SiO_2 -“Fe_2O_3 ” system with CaO/SiO_2 in 1.1 and PbO/(CaO+SiO_2) in 2.4 weight ratios, respectively, was carried out in the temperature range 1100-1300 deg C (1373-1573 K). High temperature phases were determined by the equilibrium-quenching method. Results are presented in the form of pseudo-ternary sections “Fe_2O_3 ”-ZnO-(PbO+CaO+SiO_2). X-Ray diffraction (XRD) and SEM-EDS results showed that the phase equilibria in this system are dominated by the high melting temperature spinel and zincite phases. It was observed that if the system is at a temperature below 1300 deg C and the total (Fe_2O_3 + ZnO) is greater than 20 wt%, spinel and/or zincite will be present in the slag system. As an application of the phase diagram, the liquid phase compositions below the liquidus surface were estimated, then their viscosities were calculated using FACTSage software. (author)

Photocatalytic decomposition of N{sub 2}O over TiO{sub 2}/g-C{sub 3}N{sub 4} photocatalysts heterojunction

Energy Technology Data Exchange (ETDEWEB)

Kočí, K., E-mail: kamila.koci@vsb.cz [Institute of Environmental technologies, VŠB Technical University of Ostrava 17. listopadu 15/2172, 708 00 Ostrava (Czech Republic); Reli, M.; Troppová, I.; Šihor, M. [Institute of Environmental technologies, VŠB Technical University of Ostrava 17. listopadu 15/2172, 708 00 Ostrava (Czech Republic); Kupková, J. [Nanotechnology center, VŠB Technical University of Ostrava 17. listopadu 15/2172, 708 00 Ostrava (Czech Republic); Kustrowski, P. [Faculty of Chemistry, Jagiellonian University in Kraków, ul. Ingardena 3, 30-060 Kraków (Poland); Praus, P. [Institute of Environmental technologies, VŠB Technical University of Ostrava 17. listopadu 15/2172, 708 00 Ostrava (Czech Republic); Department of Chemistry, VŠB Technical University of Ostrava 17. listopadu 15/2172, 708 00 Ostrava (Czech Republic)

2017-02-28

Highlights: • TiO{sub 2}/g-C{sub 3}N{sub 4} photocatalysts with the various TiO{sub 2}/g-C{sub 3}N{sub 4} weight ratios. • N{sub 2}O photocatalytic decomposition under UVC and UVA irradiation. • Heterojunction on the TiO{sub 2}/g-C{sub 3}N{sub 4} interface play an important role. • Optimal ratio of TiO{sub 2}:g-C{sub 3}N{sub 4} was 1:2 for the highest activity at UVA irradiation. - Abstract: TiO{sub 2}/g-C{sub 3}N{sub 4} photocatalysts with the various TiO{sub 2}/g-C{sub 3}N{sub 4} weight ratios from 1:2 to 1:6 were fabricated by mechanical mixing in water suspension followed by calcination. Pure TiO{sub 2} was prepared by thermal hydrolysis and pure g-C{sub 3}N{sub 4} was prepared from commercial melamine by thermal annealing at 620 °C. All the nanocomposites were characterized by X-ray powder diffraction, UV–vis diffuse reflectance spectroscopy, Raman spectroscopy, infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, photoelectrochemical measurements and nitrogen physisorption. The prepared mixtures along with pure TiO{sub 2} and g-C{sub 3}N{sub 4} were tested for the photocatalytic decomposition of nitrous oxide under UVC (λ = 254 nm), UVA (λ = 365 nm) and Vis (λ > 400 nm) irradiation. The TiO{sub 2}/g-C{sub 3}N{sub 4} nanocomposites showed moderate improvement compared to pure g-C{sub 3}N{sub 4} but pure TiO{sub 2} proved to be a better photocatalyst under UVC irradiation. However, under UVA irradiation conditions, the photocatalytic activity of TiO{sub 2}/g-C{sub 3}N{sub 4} (1:2) nanocomposite exhibited an increase compared to pure TiO{sub 2}. Nevertheless, further increase of g-C{sub 3}N{sub 4} amount leads/led to a decrease in reactivity. These results are suggesting the nanocomposite with the optimal weight ratio of TiO{sub 2} and g-C{sub 3}N{sub 4} have shifted absorption edge energy towards longer wavelengths and decreased the recombination rate of charge carriers compared to pure g-C{sub 3}N{sub 4}. This is

Twin-cuvette measurement technique for investigation of dry deposition of O3 and PAN to plant leaves under controlled humidity conditions

Science.gov (United States)

Sun, Shang; Moravek, Alexander; von der Heyden, Lisa; Held, Andreas; Sörgel, Matthias; Kesselmeier, Jürgen

2016-02-01

We present a dynamic twin-cuvette system for quantifying the trace-gas exchange fluxes between plants and the atmosphere under controlled temperature, light, and humidity conditions. Compared with a single-cuvette system, the twin-cuvette system is insensitive to disturbing background effects such as wall deposition. In combination with a climate chamber, we can perform flux measurements under constant and controllable environmental conditions. With an Automatic Temperature Regulated Air Humidification System (ATRAHS), we are able to regulate the relative humidity inside both cuvettes between 40 and 90 % with a high precision of 0.3 %. Thus, we could demonstrate that for a cuvette system operated with a high flow rate (> 20 L min-1), a temperature-regulated humidification system such as ATRAHS is an accurate method for air humidification of the flushing air. Furthermore, the fully automatic progressive fill-up of ATRAHS based on a floating valve improved the performance of the entire measurement system and prevented data gaps. Two reactive gas species, ozone (O3) and peroxyacetyl nitrate (PAN), were used to demonstrate the quality and performance of the twin-cuvette system. O3 and PAN exchange with Quercus ilex was investigated over a 14 day measurement period under controlled climate chamber conditions. By using O3 mixing ratios between 32 and 105 ppb and PAN mixing ratios between 100 and 350 ppt, a linear dependency of the O3 flux as well as the PAN flux in relation to its ambient mixing ratio could be observed. At relative humidity (RH) of 40 %, the deposition velocity ratio of O3 and PAN was determined to be 0.45. At that humidity, the deposition of O3 to the plant leaves was found to be only controlled by the leaf stomata. For PAN, an additional resistance inhibited the uptake of PAN by the leaves. Furthermore, the formation of water films on the leaf surface of plants inside the chamber could be continuously tracked with our custom built leaf wetness sensors

Aviation NOx-induced CH4 effect: Fixed mixing ratio boundary conditions versus flux boundary conditions

Science.gov (United States)

Khodayari, Arezoo; Olsen, Seth C.; Wuebbles, Donald J.; Phoenix, Daniel B.

2015-07-01

Atmospheric chemistry-climate models are often used to calculate the effect of aviation NOx emissions on atmospheric ozone (O3) and methane (CH4). Due to the long (∼10 yr) atmospheric lifetime of methane, model simulations must be run for long time periods, typically for more than 40 simulation years, to reach steady-state if using CH4 emission fluxes. Because of the computational expense of such long runs, studies have traditionally used specified CH4 mixing ratio lower boundary conditions (BCs) and then applied a simple parameterization based on the change in CH4 lifetime between the control and NOx-perturbed simulations to estimate the change in CH4 concentration induced by NOx emissions. In this parameterization a feedback factor (typically a value of 1.4) is used to account for the feedback of CH4 concentrations on its lifetime. Modeling studies comparing simulations using CH4 surface fluxes and fixed mixing ratio BCs are used to examine the validity of this parameterization. The latest version of the Community Earth System Model (CESM), with the CAM5 atmospheric model, was used for this study. Aviation NOx emissions for 2006 were obtained from the AEDT (Aviation Environmental Design Tool) global commercial aircraft emissions. Results show a 31.4 ppb change in CH4 concentration when estimated using the parameterization and a 1.4 feedback factor, and a 28.9 ppb change when the concentration was directly calculated in the CH4 flux simulations. The model calculated value for CH4 feedback on its own lifetime agrees well with the 1.4 feedback factor. Systematic comparisons between the separate runs indicated that the parameterization technique overestimates the CH4 concentration by 8.6%. Therefore, it is concluded that the estimation technique is good to within ∼10% and decreases the computational requirements in our simulations by nearly a factor of 8.

Measurement of glass transition temperature, residual heat of reaction and mixing ratio of epoxy resins using near infrared spectroscopy: a preliminary study

DEFF Research Database (Denmark)

Houmøller, Lars Plejdrup; Laursen, Peter Clemen

2003-01-01

As a measure of the degree of curing of epoxy resins, the glass transition temperature, Tg, and the residual heat of reaction, DeltaHr, are often used. In this study, near infrared spectroscopy and multivariate calibration (partial least squares regression (PLSR)) have been used to monitor the two...... variables, using differential scanning calorimetry (DSC) as the reference method. The epoxy under study was a commercial system consisting of the resin, trimethylolpropanetriglycidylether, and the hardener, 3-aminomethyl-3,5,5,-trimethylcyclohexylamine. Using samples cured under different conditions......, calibrations resulted in root mean square errors of cross-validation (RMSECV) of 18 J/g for DeltaHr (range for Hr: 6.1-231.3 J/g) and 7.2ºC for Tg (range for Tg: 41.5-98.8ºC). Also, a PLSR model for mixing ratio of hardener and resin was obtained, resulting in a RMSECV of 0.0040 (range for mixing ratio: 0.180-0.380)...

Homogeneity of peraluminous SiO2-B2O3-Al2O3-Na2O-CaO-Nd2O3 glasses: Effect of neodymium content

International Nuclear Information System (INIS)

Gasnier, E.; Bardez-Giboire, I.; Massoni, N.; Montouillout, V.; Pellerin, N.; Allix, M.; Ory, S.; Cabie, M.; Poissonnet, S.; Massiot, D.

2014-01-01

Considering the interest of developing new glass matrices able to immobilize higher concentration of high level nuclear wastes than currently used nuclear borosilicate compositions, glasses containing high rare earth contents are of particular interest. This study focuses on a peraluminous alumino borosilicate system SiO 2 -B 2 O 3 -Al 2 O 3 -Na 2 O-CaO-Nd 2 O 3 defined by a per-alkaline/peraluminous ratio RP = ([Na 2 O] + [CaO])/ ([Na 2 O] + [CaO] + [Al 2 O 3 ]) ≤ 0.5. Samples with various contents of Nd 2 O 3 from 0 to 10 mol% were studied using DSC, XRD, SEM, TEM, STEM and EMPA methods. The glasses present a high thermal stability even after a slow cooling treatment from the melt. Only a slight mullite crystallization is detected for low Nd 2 O 3 content (≤2.3 mol%) and crystallization of a neodymium borosilicate crystalline phase combined to a phase separation occurred at high Nd 2 O 3 content (≥8 mol%). The solubility of neodymium in the presence of aluminum is demonstrated, with higher neodymium incorporation amounts than in per-alkaline glasses. (authors)

Crystallization of mordenite zeolite with seed addition in reaction mixtures with different SiO{sub 2}/Al{sub 2}O{sub 3} ratios; Cristalizacao da zeolita mordenita com adicao de sementes em meio reacionais com diferentes razoes SiO{sub 2}/Al{sub 2}O{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Cysneiros, O.M.S.; Silva, B.J.B.; Silva, A.O.S.; Alencar, S.L.; Santos, R.B.; Soares, P.F.M.; Mendonca, T.R.D.; Sousa Junior, L.V.; Santos, J.R., E-mail: brunojbarros@hotmail.com [Universidade Federal de Alagoas (UFAL), Maceio (Brazil). Departamento de Engenharia Quimica. Laboratorio de Sintese de Catalisadores

2016-04-15

The synthesis of samples of mordenite were performed using the hydrothermal method using two different types of crystallization seed (mordenite and ferrierite), where they were exploited to change some parameters of the synthesis, such as SiO{sub 2}/Al{sub 2}O{sub 3} = 20, 60 and 100 and the ratio OH/SiO{sub 2} = 0.2, 0.3 and 0.4, at different times of crystallization, at a temperature of 170 °C. The samples were characterized by X-ray diffraction (XRD), thermogravimetric analysis (TGA/DTA), nitrogen adsorption at -196 °C (BET) and temperature programmed desorption of ammonia (NH{sub 3}-TPD). It was found that the use of the ratio OH/SiO{sub 2} = 0.4, together with the seeds of the most MOR and FER crystalline samples were obtained, demonstrating the critical role of mineralizing agent OH{sup -} in the middle. (author)

Synthesis and properties of γ-Ga2O3-Al2O3 solid solutions

Science.gov (United States)

Afonasenko, T. N.; Leont'eva, N. N.; Talzi, V. P.; Smirnova, N. S.; Savel'eva, G. G.; Shilova, A. V.; Tsyrul'nikov, P. G.

2017-10-01

The textural and structural properties of mixed oxides Ga2O3-Al2O3, obtained via impregnating γ-Al2O3 with a solution of Ga(NO3)3 and subsequent heat treatment, are studied. According to the results from X-ray powder diffraction, gallium ions are incorporated into the structure of aluminum oxide to form a solid solution of spinel-type γ-Ga2O3-Al2O3 up to a Ga2O3 content of 50 wt % of the total weight of the sample, accompanied by a reduction in the specific surface area, volume, and average pore diameter. It is concluded that when the Ga2O3 content exceeds 50 wt %, the β-Ga2O3 phase is observed along with γ-Ga2O3-Al2O3 solid solution. 71Ga and 27Al NMR spectroscopy shows that gallium replaces aluminum atoms from the tetrahedral position to the octahedral coordination in the structure of γ-Ga2O3-Al2O3.

Ternary mixed metal Fe-doped NiCo2O4 nanowires as efficient electrocatalysts for oxygen evolution reaction

Science.gov (United States)

Yan, Kai-Li; Shang, Xiao; Li, Zhen; Dong, Bin; Li, Xiao; Gao, Wen-Kun; Chi, Jing-Qi; Chai, Yong-Ming; Liu, Chen-Guang

2017-09-01

Designing mixed metal oxides with unique nanostructures as efficient electrocatalysts for water electrolysis has been an attractive approach for the storage of renewable energies. The ternary mixed metal spinel oxides FexNi1-xCo2O4 (x = 0, 0.1, 0.25, 0.5, 0.75, 0.9, 1) have been synthesized by a facile hydrothermal approach and calcination treatment using nickel foam as substrate. Fe/Ni ratios have been proved to affect the nanostructures of FexNi1-xCo2O, which imply different intrinsic activity for oxygen evolution reaction (OER). SEM images show that Fe0.5Ni0.5Co2O4 has the uniform nanowires morphology with about 30 nm of the diameter and 200-300 nm of the length. The OER measurements show that Fe0.5Ni0.5Co2O4 exhibits the better electrocatalytic performances with lower overpotential of 350 mV at J = 10 mA cm-2. In addition, the smaller Tafel slope of 27 mV dec-1 than other samples with different Fe/Ni ratios for Fe0.5Ni0.5Co2O4 is obtained. The improved OER activity of Fe0.5Ni0.5Co2O4 may be attributed to the synergistic effects from ternary mixed metals especially Fe-doping and the uniform nanowires supported on NF. Therefore, synthesizing Fe-doped multi-metal oxides with novel nanostructures may be a promising strategy for excellent OER electrocatalysts and it also provides a facile way for the fabrication of high-activity ternary mixed metal oxides electrocatalysts.

Combined Effect of Contraction Ratio and Chamber Pressure on the Performance of a Gaseous Hydrogen-Liquid-Oxygen Combustor for a Given Propellant Weight Flow and Oxidant-Fuel Ratio

Science.gov (United States)

Hersch, Martin

1961-01-01

The effect of contraction ratio and chamber pressure on the combustion performance of a gaseous-hydrogen-liquid-oxygen combustor was investigated analytically and experimentally. The experiment was conducted with a "two-dimensional" gaseous-hydrogen-liquid-oxygen engine of about 150-pound thrust. The contraction ratio was varied from 1.5 to 6 by changing the nozzle throat area. This variation resulted in a chamber pressure variation of about 25 to 120 pounds per square inch. The experimental results were corrected for heat transfer to the engine walls and momentum pressure losses. The experimental performance, as evaluated in terms of characteristic exhaust velocity, was 98 percent of theoretical at contraction ratios greater than 3 but decreased very rapidly at smaller contraction ratios. The heat-transfer rate increased with increasing contraction ratio and chamber pressure; it was about 1 Btu per square inch per second at a contraction ratio of 1.5 and increased to about 3 at a contraction ratio of 6. The combined effects of contraction-ratio and chamber-pressure changes on performance were investigated analytically with a mixing model and a vaporization model. The mixing model predicted very poor mixing at contraction ratios below 3 and almost perfect mixing at higher contraction ratios. The performance predicted by the vaporization model was very close to 100 percent for all contraction ratios. From these results, it was concluded that the performance was limited by poor mixing at low contraction ratios and chamber pressures.

Porous ZnCo 2 O 4 nanoparticles derived from a new mixed-metal organic framework for supercapacitors

KAUST Repository

Chen, Siru

2015-01-01

Cobalt-based oxides have been shown to be promising materials for application in high-energy-density Li-ion batteries and supercapacitors. In this paper, we report a new and simple strategy for the synthesis of a mixed-metal spinel phase (ZnCo2O4) from a zinc and cobalt mixed-metal organic framework (JUC-155). It is important to rationally design a MOF with a precise ratio (Co/Zn) and a synthetic process that is simple and time saving. After solid-state annealing of the mixed-metal MOF precursor at 400 °C for two hours, a pure ZnCo2O4 phase with a high surface area (55 cm2 g−1) was obtained. When used as electrode materials for supercapacitors, an exceptionally high specific capacitance of 451 F g−1 was obtained at the scan rate of 5 mV s−1. The capacitance loss after 1500 cycles was only 2.1% at a current density of 2 A g−1, indicating that this phase has an excellent cycling stability. These remarkable electrochemical performances suggest that this phase is potentially promising for application as an efficient electrode in electrochemical capacitors.

A non-equilibrium ortho-to-para ratio of H2O in the Orion PDR

NARCIS (Netherlands)

Choi, Yunhee; van der Tak, Floris; Bergin, Edwin; Plume, Rene

The ortho-to-para ratio (OPR) of H2O is lower than 1 at low temperature (<15 K) and increases to 3 at high temperature (> 40 K). The OPR of H2O is thus useful to study the formation mechanism of water. The measured OPRs of H2O is 2-3 in solar system comets (Mumma & Charnley, 2011) and in the

Electrodeposited Mn3O4-NiO-Co3O4 as a composite electrode material for electrochemical capacitor

International Nuclear Information System (INIS)

Rusi; Majid, S.R.

2015-01-01

Highlights: • Composite electrodes were synthesized by in situ electrodeposition method. • The highest specific capacitance of composite electrode is 7404 F g −1 . • The power density of composite electrode is 99 kW kg −1 at current density of 20 A g −1 . • The addition of K 3 Fe(CN) 6 in KOH electrolyte has improved the electrochemical performance. - Abstract: A simple and easy galvanostatic electrodeposition method is used to synthesise a composite electrode consisting of manganese oxide (Mn 3 O 4 ), nickel oxide (NiO) and cobalt oxide (Co 3 O 4 ). The influence of Co 3 O 4 on the morphology of fixed Mn 3 O 4 -NiO particles is investigated with a field emission scanning electron microscope (FESEM) and transmission electron microscope (TEM). The nature and elemental of the composite are examined by means of X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDX). The electrochemical performances of an Mn 3 O 4 -NiO-Co 3 O 4 nanostructure/SS composite electrode are studied by cyclic voltammetry (CV) and galvanostatic charge-discharge (CD) in various electrolytes, i.e. 0.5 M Na 2 SO 4 , 0.5 M KOH, 0.5 M Na 2 SO 4 /0.04 M K 3 Fe(CN) 6 and 0.5 M KOH/0.04 M K 3 Fe(CN) 6 electrolytes. The composite electrode prepared from 0.15 M Co deposition solution exhibits the optimum specific capacitance of 7404 F g −1 with high energy and power density of 1028 Wh kg −1 and 99 kW kg −1 at 20 A g −1 in mix KOH/0.04 M K 3 Fe(CN) 6 electrolyte, respectively. The results show that the incorporation of K 3 Fe(CN) 6 in KOH electrolyte influences the capacitance of Mn 3 O 4 -NiO-Co 3 O 4 composite electrodes

Lead-free LiNbO3 nanowire-based nanocomposite for piezoelectric power generation

Science.gov (United States)

2014-01-01

In a flexible nanocomposite-based nanogenerator, in which piezoelectric nanostructures are mixed with polymers, important parameters to increase the output power include using long nanowires with high piezoelectricity and decreasing the dielectric constant of the nanocomposite. Here, we report on piezoelectric power generation from a lead-free LiNbO3 nanowire-based nanocomposite. Through ion exchange of ultra-long Na2Nb2O6-H2O nanowires, we synthesized long (approximately 50 μm in length) single-crystalline LiNbO3 nanowires having a high piezoelectric coefficient (d33 approximately 25 pmV-1). By blending LiNbO3 nanowires with poly(dimethylsiloxane) (PDMS) polymer (volume ratio 1:100), we fabricated a flexible nanocomposite nanogenerator having a low dielectric constant (approximately 2.7). The nanogenerator generated stable electric power, even under excessive strain conditions (approximately 105 cycles). The different piezoelectric coefficients of d33 and d31 for LiNbO3 may have resulted in generated voltage and current for the e33 geometry that were 20 and 100 times larger than those for the e31 geometry, respectively. This study suggests the importance of the blending ratio and strain geometry for higher output-power generation in a piezoelectric nanocomposite-based nanogenerator. PACS 77.65.-j; 77.84.-s; 73.21.Hb PMID:24386884

Luminescence and energy transfer of Tb3+-doped BaO-Gd2O3-Al2O3-B2O3-SiO2 glasses.

Science.gov (United States)

Zuo, Chenggang; Huang, Jinze; Liu, Shaoyou; Xiao, Anguo; Shen, Youming; Zhang, Xiangyang; Zhou, Zhihua; Zhu, Ligang

2017-12-05

Transparent Tb 3+ -doped BaO-Gd 2 O 3 -Al 2 O 3 -B 2 O 3 -SiO 2 glasses with the greater than 4g/cm 3 were prepared by high temperature melting method and its luminescent properties have been investigated by measured UV-vis transmission, excitation, emission and luminescence decay spectra. The transmission spectrum shows there are three weak absorption bands locate at about 312, 378 and 484nm in the glasses and it has good transmittance in the visible spectrum region. Intense green emission can be observed under UV excitation. The effective energy transfer from Gd 3+ ion to Tb 3+ ion could occur and sensitize the luminescence of Tb 3+ ion. The green emission intensity of Tb 3+ ion could change with the increasing SiO 2 /B 2 O 3 ratio in the borosilicate glass matrix. With the increasing concentration of Tb 3+ ion, 5 D 4 → 7 F J transitions could be enhanced through the cross relaxation between the two nearby Tb 3+ ions. Luminescence decay time of 2.12ms from 546nm emission is obtained. The results indicate that Tb 3+ -doped BaO-Gd 2 O 3 -Al 2 O 3 -B 2 O 3 -SiO 2 glasses would be potential scintillating material for applications in X-ray imaging. Copyright © 2017 Elsevier B.V. All rights reserved.

Biodiesel synthesis by TiO2-ZnO mixed oxide nanocatalyst catalyzed palm oil transesterification process.

Science.gov (United States)

Madhuvilakku, Rajesh; Piraman, Shakkthivel

2013-12-01

Biodiesel is a promising alternating environmentally benign fuel to mineral diesel. For the development of easier transesterification process, stable and active heterogeneous mixed metal oxide of TiO2-ZnO and ZnO nanocatalysts were synthesized and exploited for the palm oil transesterification process. The synthesized catalysts were characterized by XRD, FT-IR, and FE-SEM studies for their structural and morphological characteristics. It was found that TiO2-ZnO nanocatalyst exhibits good catalytic activity and the catalytic performance was greatly depends on (i) catalyst concentration (ii) methanol to oil molar ratio (iii) reaction temperature and (iv) reaction time. A highest 98% of conversion was obtained at the optimum reaction parameters with 200 mg of catalyst loading and the biodiesel was analyzed by TLC and (1)H NMR techniques. The TiO2-ZnO nanocatalyst shows good catalytic performance over the ZnO catalyst, which could be a potential candidate for the large-scale biodiesel production from palm oil at the reduced temperature and time. Copyright © 2013. Published by Elsevier Ltd.

Optimum O2:CH4 Ratio Promotes the Synergy between Aerobic Methanotrophs and Denitrifiers to Enhance Nitrogen Removal

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Jing Zhu

2017-06-01

Full Text Available The O2:CH4 ratio significantly effects nitrogen removal in mixed cultures where aerobic methane oxidation is coupled with denitrification (AME-D. The goal of this study was to investigate nitrogen removal of the AME-D process at four different O2:CH4 ratios [0, 0.05, 0.25, and 1 (v/v]. In batch tests, the highest denitrifying activity was observed when the O2:CH4 ratio was 0.25. At this ratio, the methanotrophs produced sufficient carbon sources for denitrifiers and the oxygen level did not inhibit nitrite removal. The results indicated that the synergy between methanotrophs and denitrifiers was significantly improved, thereby achieving a greater capacity of nitrogen removal. Based on thermodynamic and chemical analyses, methanol, butyrate, and formaldehyde could be the main trophic links of AME-D process in our study. Our research provides valuable information for improving the practical application of the AME-D systems.

Development on UO3-K2O and MoO3-K2O binary systems and study of UO2MoO4-MoO3 domain within UO3-MoO3-K2O ternary system

International Nuclear Information System (INIS)

Dion, C.; Noel, A.

1983-01-01

This paper confirms the previous study on the MoO 3 -K 2 O system, and constitutes a clarity of the UO 3 -K 2 O system. Four distinct uranates VI with alkaline metal/uranium ratio's 2, 1, 0,5 and 0,285 exist. Preparation conditions and powder diffraction spectra of these compounds are given. Additional informations relative to K 2 MoO 4 allotropic transformations are provided. Study of UO 2 MoO 4 -K 2 MoO 4 diagram has brought three new phases into prominence: (B) K 6 UMo 4 O 18 incongruently melting point, (E) K 2 UMo 2 O 10 congruently melting and (F) K 2 U 3 Mo 4 O 22 incongruently melting point. Within MoO 3 -K 2 MoO 4 -UO 2 MoO 4 ternary system, no new phase is found. The general appearance of ternary liquidus and crystallization fields of several compounds are given. These three new compounds become identified with these of UO 2 MoO 4 -Na 2 MoO 4 binary system [fr

Spatial variability of mixing ratios of ammonia and tracer gases in a naturally ventilated dairy cow barn

NARCIS (Netherlands)

Mendes, Luciano B.; Edouard, Nadège; Ogink, Nico W.M.; Dooren, van Hendrik Jan C.; Fátima F. TinÔco, de Ilda; Mosquera Losada, Julio

2015-01-01

The use of the tracer gas ratio method to estimate emissions from naturally ventilated (NV) livestock barns excludes the need of monitoring ventilation rates. However, it requires accurate measurement of tracer release rate (Q_T) and a representative estimate of the mixing ratio between

Responses of mixed methanotrophic consortia to variable Cu2+/Fe2+ ratios.

Science.gov (United States)

Chidambarampadmavathy, Karthigeyan; Karthikeyan, Obulisamy Parthiba; Huerlimann, Roger; Maes, Gregory E; Heimann, Kirsten

2017-07-15

Methane mitigation in landfill top cover soils is mediated by methanotrophs whose optimal methane (CH 4 ) oxidation capacity is governed by environmental and complex microbial community interactions. Optimization of CH 4 remediating bio-filters need to take microbial responses into account. Divalent copper (Cu 2+ ) and iron (Fe 2+ ) are present in landfills at variable ratios and play a vital role in methane oxidation capacity and growth of methanotrophs. This study, as a first of its kind, therefore quantified effects of variable Cu 2+ and Fe 2+ (5:5, 5:25 and 5:50 μM) ratios on mixed methanotrophic communities enriched from landfill top cover (LB) and compost soils (CB). CH 4 oxidation capacity, CH 4 removal efficiencies, fatty acids content/profiles and polyhydroxybutyrate (PHB; a biopolymer) contents were also analysed to quantify performance and potential co-product development. Mixed methanotroph cultures were raised in 10 L continuous stirred tank reactors (CSTRs, Bioflo ® & Celligen ® 310 Fermentor/Bioreactor; John Morris Scientific, Chatswood, NSW, Australia). Community structure was determined by amplifying the V3-V4 region of 16s rRNA gene. Community structure and, consequently, fatty acid-profiles changed significantly with increasing Cu 2+ /Fe 2+ ratios, and responses were different for LB and CB. Effects on methane oxidation capacities and PHB content were similar in the LB- and CB-CSTR, decreasing with increasing Cu 2+ /Fe 2+ ratios, while biomass growth was unaffected. In general, high Fe 2+ concentration favored growth of the type -II methanotroph Methylosinus in the CB-CSTR, but methanotroph abundances decreased in the LB-CSTR. Increase in Cu 2+ /Fe 2+ ratio increased the growth of Sphingopyxis in both systems, while Azospirllum was co-dominant in the LB- but absent in the CB-CSTR. After 13 days, methane oxidation capacities and PHB content decreased by ∼50% and more in response to increasing Fe 2+ concentrations. Although methanotroph

Control device of air-fuel ratio of alcohol-gasoline mixed fuel

Energy Technology Data Exchange (ETDEWEB)

Takahashi, Kazuo

1987-08-19

Concerning alcohol-gasoline mixed fuel, even the same amount of the fuel shows different air-fuel ratio depending upon alcohol concentration in the fuel, accordingly it is required to know the alcohol concentration when it is intended to make the air-fuel ratio to be the same as the predetermined ratio. Although a sensor which can detect in quick response and exactly the alcohol concentration has not been developed, the alcohol concentration in gasoline can be detected by detecting the concentration of the water in exhaust gas and many hygrometers which can detect the concentration of the water with high precision are available. With regard to an internal combustion engine equipped with a fuel supply device in order to supply alcohol-gasoline mixed fuel into an engine suction passage, this invention offers an air-fuel ratio control device to control the amount of the fuel to be supplied from the fuel supply device by detecting the concentration of alcohol in the gasoline from among the output signals of the main hygrometer and the auxiliary hygrometer. The former hygrometer to detect the concentration of the water in the exhaust gas is set in the engine exhaust gas passage and the latter is installed to detect the concentration of the water in the air. (4 figs)

E2,M1 multipole mixing ratios in even--even nuclei, A greater than or equal to 152

International Nuclear Information System (INIS)

Krane, K.S.

1975-01-01

A survey is presented of E2,M1 mixing ratios of gamma-ray transitions in even-even nuclei with mass numbers A greater than or equal to 152. Angular distribution and correlation data from the literature are analyzed in terms of a consistent choice of the phase relationship between the E2 and M1 matrix elements. The cutoff date for the literature was June 1975. Based on an average of the experimental results from the literature, a recommended value of the E2,M1 mixing ratio for each transition is included

Laser-based measurements of 18O/16O stable isotope ratios (δ18O in wine samples

Directory of Open Access Journals (Sweden)

Gupta M

2013-09-01

Full Text Available Manish Gupta,1 J Brian Leen,1 Elena Simone Franklin Berman,1 Aldo Ciambotti2 1Los Gatos Research, Mountain View, CA, USA; 2Consiglio per la Ricerca e la Sperimentazione in Agricoltura, Centro di Ricerca per l'Enologia, Asti, Italy Abstract: Wine counterfeiting is an international, multi-billion dollar issue, with some estimates suggesting that up to 5% of wines sold at auctions or secondary markets are fraudulent. Isotope ratio mass spectrometer (IRMS measurements of the 18O/16O stable isotope ratio (δ18O of water-in-wine have been used for wine authentication; however, these analyses are time-consuming and costly. In this preliminary study, off-axis integrated cavity output spectroscopy (OA-ICOS is used to quantify δ18O in wines. This laser-based method has been extensively used to study water isotopes for hydrological and medical applications. Recently, the development of a spectral contaminant identifier (SCI has extended the application of these OA-ICOS analyzers to contaminated water samples (eg, plant, soil, and leaf waters. Here, we utilize OA-ICOS with the SCI to characterize wine samples (9%–15% ethanol, and show that the laser-based instrument provides a δ18O measurement precision of ±0.07‰ (1σ and agrees with IRMS to within ±0.63‰ (1σ. Moreover, by training the SCI on isotopically-characterized wines, the agreement with IRMS improves to within ±0.30‰ (1σ. The utility of the instrument is demonstrated by measuring watered and mixed wines. The method presented here can be readily extended to address other food authentication applications. Keywords: wine isotopes, wine fraud, counterfeit wines, OA-ICOS

Bending strength of glass-ceramics based on 3CaO.P2O5-SiO2-MgO glass system

International Nuclear Information System (INIS)

Daguano, J.K.M.F.; Suzuki, P.A.; Santos, C.; Fernandes, M.H.V.; Elias, C.N.

2009-01-01

In this work, the Modulus of Rupture of bioactive glass-ceramic based on 3CaO.P 2 O 5 -SiO 2 -MgO system was investigated, aiming its use in bone-restorations. The mechanical property was correlated with microstructural and crystallographic features of this material. High-purity starting-powders, CaCO 3 , SiO 2 , MgO, Ca (H 2 PO 4 ).H 2 O, were used in this study. The powders were mixed in a stoichiometric ratio, using planetary ball-mill. The suspensions were dried, sieved and melted at 1600 deg C, for 4h. The casting ones were cooled quickly until annealing temperature 700 deg C, in which remained for 2h, with controlled cooling-rate until ambient temperature. Bulks of glass were heat-treated with temperatures varying between 700 deg C and 1100 deg C, for 4h, being after that, cooled at 3 deg C/min. Bioactive glass and glass-ceramic were characterized by HRXRD (high resolution X-ray diffraction), where whitlockite was main phase. The microstructure was analyzed by scanning electronic microscopy. Modulus of Rupture was determined by four-point bending testing using specimens of 1.5 x 2 x 25 mm and glasses presented strength near to 70MPa, while glass ceramics treated at 975 deg C-4h, presented bending strength of 120MPa. (author)

Al2O3-Cact-(CuO, Cr2O3, Co3O4 Adsorbents-Catalysts: Preparation and Characterization

Directory of Open Access Journals (Sweden)

Gitana DABRILAITĖ-KUDŽMIENĖ

2013-03-01

Full Text Available Al2O3-Cact-(CuO, Cr2O3 Co3O4 adsorbents-catalysts were prepared using Al2O3-Cact (alumina gel–activated carbon adsorbent and different amount of CuO, Cr2O3 and Co3O4. The active components were incorporated into wet alumina gel–carbon mixture using different conditions (by sol-gel method and mixing a milled metal oxides. Equilibrium adsorptive capacity measurements of alcohol vapours were carried out in order to determine the influence of preparation conditions on the stability of prepared adsorbents–catalysts. Specific surface area of the prepared adsorbents-catalysts were measured by BET method. It was established that for adsorbent-catalyst produced by sol-gel method SBET = 244.7 m2/g. Surface area SBET = 29.32 m2/g was obtained for adsorbent-catalyst with metal oxides. On the basis of these results it was assumed that active carbon was lost in this adsorbent-catalyst during the preparation process. Sol-gel derived adsorbent–catalyst was tested for the oxidation of methanol vapours. Catalytic oxidation was carried out in fixed-bed reactor. Experimental data indicate that adsorptive capacity of the adsorbent–catalyst is (3.232 – 3.259 mg/m3 CH3OH at relative air humidity is 40 % – 50 %. During a fast heating of CH3OH – saturated adsorbent-catalyst a part of adsorbate is converted to CO2 and H2O. Methanol conversion increases with increasing of adsorbent-catalyst heating rate.DOI: http://dx.doi.org/10.5755/j01.ms.19.1.3832

The preparation and characterization of nanostructured TiO2-ZrO2 mixed oxide electrode for efficient dye-sensitized solar cells

International Nuclear Information System (INIS)

Kitiyanan, Athapol; Ngamsinlapasathian, Supachai; Pavasupree, Soropong; Yoshikawa, Susumu

2005-01-01

The preparation of nanostructured mixed metal oxide based on a sol-gel method with surfactant-assisted mechanism, and its application for dye-sensitized solar cell (DSSC) are reported. The mixed zirconia (ZrO 2 ) and titania (TiO 2 ) mesoporous powder possessed larger surface area than the corresponding titania. For the UV action spectra of unsensitized photochemical cell, the mixed zirconia/titania electrode can absorb UV light below 380nm, corresponding to band gap (E g ) around 3.27eV, which is higher than that of pure component of titania (E g =3.2eV). Both of these improved properties, i.e., BET surface area and band gap, contributed to the improvement on a short-circuit photocurrent up to 11%, an open-circuit voltage up to 4%, and a solar energy conversion efficiency up to 17%, for the DSSC fabricated by mesoporous zirconia/titania mixed system when compared to the cell that was fabricated only by nanostructured TiO 2 . The cell fabricated by 5μm thick mixed TiO 2 -ZrO 2 electrode gave the short-circuit photocurrent about 13mA/cm 2 , open-circuit voltage about 600 mV and the conversion efficiency 5.4%

Al{sub 2}O{sub 3} reinforced nanoparticle ZrO{sub 2} (3at%?Y{sub 2}O{sub 3}); Al{sub 2}O{sub 3} reforcado com nanoparticulas de ZrO{sub 2}(3%mol Y{sub 2}O{sub 3})

Energy Technology Data Exchange (ETDEWEB)

Cossu, C.M.F.A.; Alves, M.F.R.P.; Campos, L.Q.B.; Magnago, R.O.; Santos, C., E-mail: caio.cossu@usp.br [Universidade do Estado do Rio de Janeiro (UERJ), Resende, RJ (Brazil). Faculdade de Tecnologia; Simba, B.G. [Universidade Estadual Paulista Julio de Mesquita Filho (UNESP), Guaratingueta, SP (Brazil). Faculdade de Engenharia

2016-07-01

This work developed a composite Al{sub 2}O{sub 3}-based reinforced with nanoparticles of ZrO{sub 2} (Y{sub 2}O{sub 3}), to evaluate the effect of the content of ZrO{sub 2} nanoparticles (Y{sub 2}O{sub 3}) on the mechanical properties. Mixtures containing a matrix of Al{sub 2}O{sub 3} with fractions in weight of 3%, 5%, 10% and 15%, ZrO{sub 2} (Y{sub 2}O{sub 3}), and were mixed in mortar mill. Mixtures received 5% polymeric binder (PVA); and after adding the binder, the material was pressed uniaxially to 50MPa, and then sintered at a temperature of 1600 ° C - 2h. The sintered products were characterized by X-ray diffraction, scanning electron microscopy (SEM), relative density, hardness and fracture toughness. The results of X-ray diffraction showed that Al{sub 2}O{sub 3} and tetragonal ZrO{sub 2} as crystal phases found after sintering. Furthermore, the relative green density of 55% was predominant in the compact; and after sintering, varied depending on the ZrO{sub 2} content, reaching 97% in sintered compositions with 3% ZrO{sub 2} nanoparticles (Y{sub 2O}3). The hardness of the samples showed values of 1670HV and the maximum toughness of 3.2 MPa × m{sup 1/2}, directly influenced by the presence of nanoparticles ZrO{sub 2} uniformly dispersed in the matrix Al{sub 2}O{sub 3}, which results in at least two main mechanisms tenacifiers: transformation of tetragonal-monoclinic phase of zirconia, and compressive residual strain between the two phases present, Al{sub 2}O{sub 3} and tetragonal ZrO{sub 2}. (author)

XPS study of Li/Nb ratio in LiNbO{sub 3} crystals. Effect of polarity and mechanical processing on LiNbO{sub 3} surface chemical composition

Energy Technology Data Exchange (ETDEWEB)

Skryleva, E.A., E-mail: easkryleva@gmail.com; Kubasov, I.V., E-mail: kubasov.ilya@gmail.com; Kiryukhantsev-Korneev, Ph.V., E-mail: kiruhancev-korneev@yandex.ru; Senatulin, B.R., E-mail: borisrs@yandex.ru; Zhukov, R.N., E-mail: rom_zhuk@mail.ru; Zakutailov, K.V., E-mail: zakkonst@gmail.com; Malinkovich, M.D., E-mail: malinkovich@yandex.ru; Parkhomenko, Yu.N., E-mail: parkh@rambler.ru

2016-12-15

Highlights: • XPS Li/Nb ratio measurement uncertainty in LNbO3 specimens was obtained. • The effect of polarization on surface chemistry was observed only on cleaves. • Li/Nb ratio on positive cleave surface is higher than on negative one. • The positive cleave surface adsorbs fluorine more efficiently than negative one. • Mechanical processing of crystals reduces surface Li/Nb. - Abstract: Different sections of congruent lithium niobate (CLN) crystals have been studied using X-ray photoelectron spectroscopy (XPS). We have developed a method for measuring the lithium-to-niobium atomic ratio Li/Nb from the ratio of the Li1s and Nb4s spectral integral intensities with an overall error of within 8 %. Polarity and mechanical processing affect the Li/Nb ratio on CLN crystal surfaces. The Li/Nb ratio is within the tolerance (0.946 ± 0.074) on the negative cleave surface Z, and there is excess lithium (Li/Nb = 1.25 ± 0.10) on the positive surface. The positive surfaces of the 128° Y cut plates after long exposure to air exhibit LiOH formation indications (obvious lithium excess, higher Li1s spectral binding energy and a wide additional peak in the O1s spectrum produced by nonstructural oxygen). XPS and glow discharge optical electron spectroscopy showed that mechanical processing of differently oriented crystals (X, Z and 128° Y) and different polarities dramatically reduces the Li/Nb ratio. In situ fluorine adsorption experiments revealed the following regularities: fluorine adsorption only occurred on crystal cleaves and was not observed for mechanically processed specimens. Positive cleave surfaces have substantially higher fluorine adsorption capacity compared to negative ones.

Improving the Quality of Mixed Recycled Coarse Aggregates from Construction and Demolition Waste Using Heavy Media Separation with Fe3O4 Suspension

Directory of Open Access Journals (Sweden)

Heonchan Kang

2017-01-01

Full Text Available The primary objectives of this study are to investigate the feasibility of a heavy media separation process with magnetite (Fe3O4 suspension for upgrading the quality of mixed recycled coarse aggregates from construction and demolition waste (CDW in Korea and to determine a range of effective operating density of Fe3O4 suspension for producing high-quality RCA acceptable to structural concrete applications. For the purposes, six 200 kg recycled coarse aggregates (RCAs samples were collected from a conventional recycling plant in Korea. Subsequently, the samples were processed by a heavy media separation process using Fe3O4 suspensions with various densities from 2.65 g/cm3 to 2.40 g/cm3 with an interval of 0.05 g/cm3. Next, a series of tests was performed in the laboratory to evaluate properties of finished sink and float products from the HMS processes, including oven-dry density, absorption capacity, and physical durability. Furthermore, compressive strength of concrete cylinders (150 mm by 300 mm made of the finished sink products from Fe3O4 suspensions with three different densities (2.4, 2.5, and 2.6 g/cm3 was tested in this study. As a result, it was demonstrated that the HMS process using Fe3O4 suspension with a density ranging between 2.40 and 2.65 g/cm3 was effective for upgrading mixed CDW RCAs in Korea to high-quality RCAs acceptable for structural concrete applications.

A unique polysaccharide containing 3-O-methylarabinose and 3-O-methylgalactose from Tinospora sinensis.

Science.gov (United States)

Nagar, Shipra; Hensel, Andreas; Mischnick, Petra; Kumar, Vineet

2018-08-01

Tinospora sinensis (Lour.) Merrill is of great therapeutic significance in Indian traditional medicine. Crude polysaccharides were isolated from methanol pre-extracted stems of dried material by successive extractions with cold water, hot water and NaOH (0.25 mol/L) in 0.98, 0.55 and 0.70 % yields respectively. Cold water soluble polysaccharides (CWSP) were purified and fractionated by ion exchange chromatography on DEAE-Sephacel. Neutral polysaccharides were further fractionated on Sepharose CL6B to yield three fractions TW1, TW2, TW3. The study further focuses on structural elucidation of TW1. TW1 was obtained in 0.8 % yield relative to CWSP, with MW of 1.6 × 10 5  Da. It was composed of 3-O-methyl-arabinose, 3-O-methyl-galactose and galactose in molar ratio of 1.0:6.3:0.9 respectively. Based on per-deuteromethylation, NMR and ESI-MS analyses, TW1 was composed of 1,4-linked 3-O-methyl-β-d-galactopyranose and β-d-galactopyranose backbone with branching at O-6 of 3-O-methyl-β-d-galactosyl residues by 1,5-linked 3-O-methyl-α-l-arabinofuranoside chains. 3-O-methyl-arabinose and 3-O-methyl-galactose have first ever been reported in any polysaccharide and Tinospora genus, respectively. Copyright © 2018 Elsevier Ltd. All rights reserved.

Characterization of Organic Thin Film Solar Cells of PCDTBT : PC71BM Prepared by Different Mixing Ratio and Effect of Hole Transport Layer

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Vijay Srinivasan Murugesan

2015-01-01

Full Text Available The organic thin film solar cells (OTFSCs have been successfully fabricated using PCDTBT : PC71BM with different mixing ratios (1 : 1 to 1 : 8 and the influence of hole transport layer thickness (PEDOT : PSS. The active layers with different mixing ratios of PCDTBT : PC71BM have been fabricated using o-dichlorobenzene (o-DCB. The surface morphology of the active layers and PEDOT : PSS layer with different thicknesses were characterized by AFM analysis. Here, we report that the OTFSCs with high performance have been optimized with 1 : 4 ratios of PCDTBT : PC71BM. The power conversion efficiency (PCE = 5.17% of the solar cells was significantly improved by changing thickness of PEDOT : PSS layer. The thickness of the PEDOT : PSS layer was found to be of significant importance; the thickness of the PEDOT : PSS layer at 45 nm (higher spin speed 5000 rpm shows higher short circuit current density (Jsc and lower series resistance (Rs and higher PCE.

Pt–Al2O3 dual layer atomic layer deposition coating in high aspect ratio nanopores

International Nuclear Information System (INIS)

Pardon, Gaspard; Gatty, Hithesh K; Stemme, Göran; Wijngaart, Wouter van der; Roxhed, Niclas

2013-01-01

Functional nanoporous materials are promising for a number of applications ranging from selective biofiltration to fuel cell electrodes. This work reports the functionalization of nanoporous membranes using atomic layer deposition (ALD). ALD is used to conformally deposit platinum (Pt) and aluminum oxide (Al 2 O 3 ) on Pt in nanopores to form a metal–insulator stack inside the nanopore. Deposition of these materials inside nanopores allows the addition of extra functionalities to nanoporous materials such as anodic aluminum oxide (AAO) membranes. Conformal deposition of Pt on such materials enables increased performances for electrochemical sensing applications or fuel cell electrodes. An additional conformal Al 2 O 3 layer on such a Pt film forms a metal–insulator–electrolyte system, enabling field effect control of the nanofluidic properties of the membrane. This opens novel possibilities in electrically controlled biofiltration. In this work, the deposition of these two materials on AAO membranes is investigated theoretically and experimentally. Successful process parameters are proposed for a reliable and cost-effective conformal deposition on high aspect ratio three-dimensional nanostructures. A device consisting of a silicon chip supporting an AAO membrane of 6 mm diameter and 1.3 μm thickness with 80 nm diameter pores is fabricated. The pore diameter is reduced to 40 nm by a conformal deposition of 11 nm Pt and 9 nm Al 2 O 3 using ALD. (paper)

Pt-Al2O3 dual layer atomic layer deposition coating in high aspect ratio nanopores

Science.gov (United States)

Pardon, Gaspard; Gatty, Hithesh K.; Stemme, Göran; van der Wijngaart, Wouter; Roxhed, Niclas

2013-01-01

Functional nanoporous materials are promising for a number of applications ranging from selective biofiltration to fuel cell electrodes. This work reports the functionalization of nanoporous membranes using atomic layer deposition (ALD). ALD is used to conformally deposit platinum (Pt) and aluminum oxide (Al2O3) on Pt in nanopores to form a metal-insulator stack inside the nanopore. Deposition of these materials inside nanopores allows the addition of extra functionalities to nanoporous materials such as anodic aluminum oxide (AAO) membranes. Conformal deposition of Pt on such materials enables increased performances for electrochemical sensing applications or fuel cell electrodes. An additional conformal Al2O3 layer on such a Pt film forms a metal-insulator-electrolyte system, enabling field effect control of the nanofluidic properties of the membrane. This opens novel possibilities in electrically controlled biofiltration. In this work, the deposition of these two materials on AAO membranes is investigated theoretically and experimentally. Successful process parameters are proposed for a reliable and cost-effective conformal deposition on high aspect ratio three-dimensional nanostructures. A device consisting of a silicon chip supporting an AAO membrane of 6 mm diameter and 1.3 μm thickness with 80 nm diameter pores is fabricated. The pore diameter is reduced to 40 nm by a conformal deposition of 11 nm Pt and 9 nm Al2O3 using ALD.

Room and high temperature interactions in sodium and rubidium rich ternary nitrate mixtures of UO2(NO3)2.6H2O - NaNO3 - RbNO3

International Nuclear Information System (INIS)

Kalekar, Bhupesh B.; Reddy, A.V.R.; Raje, Naina

2016-01-01

High temperature interaction behavior of nitrates is important for characterizing different intermediate products and their thermal stabilities during the calcination of nuclear waste before their immobilization in the stable glass matrix. Mixtures of UO 2 (NO 3 ) 2 .6H 2 O (UNH) with NaNO 3 (NaN) and RbNO 3 (RbN) were prepared by mixing the weighed amounts of component nitrates and grinding gently in a mortar and pestle. The mixing and grinding of individual nitrate components in a mortar with pestle showed the agglomeration of solid particles and subsequent dissolution probably in the water of crystallization of UNH. The continued grinding and mixing showed the reappearance of the solid powder. The original yellow color of the mixture was changed to greenish yellow color. The mixtures were subjected to thermal measurements using Netzsch Thermobalance (Model No.: STA 409 PC Luxx) coupled to Bruker FTIR system (Model No.: Tensor 27) via a heated Teflon capillary (1 m long, 2 mm i.d.). TG - DTG curves of equimolar mixture are displayed. The plateau was observed on TG curve in the temperature region of 31- 250 °C. It is reported that Na(UO 2 (NO 3 ) 3 ).H 2 O and Rb(UO 2 (NO 3 ) 3 ) formed around 250 °C in the equimolar nitrate mixtures of UNH-NaN and UNH-RbN. Thermal and XRD results indicated the formation of Na(UO 2 (NO 3 ) 3 ).H 2 O and Rb(UO 2 (NO) 3 ) 3 ) even by mixing the UNH, NaN and RbN in equimolar ratios at room temperature

(Ba+Sr)/Ti ratio dependence of the dielectric properties for (Ba0.5Sr0.5)TiO3 thin films prepared by ion beam sputtering

Science.gov (United States)

Yamamichi, Shintaro; Yabuta, Hisato; Sakuma, Toshiyuki; Miyasaka, Yoichi

1994-03-01

(Ba0.5Sr0.5)TiO3 thin films were prepared by ion beam sputtering from powder targets with (Ba+Sr)/Ti ratios ranging from 0.80 to 1.50. All of the perovskite (Ba,Sr)TiO3 films were single phase except for the film with a (Ba+Sr)/Ti ratio of 1.41. The dielectric constant values notably depended on the (Ba+Sr)/Ti ratio for films thicker than 70 nm. The highest dielectric constant of 580 was achieved for the 5% (Ba+Sr) rich film. This (Ba+Sr)/Ti ratio dependence was diminished by the thickness dependence for thinner films. The grain sizes for the 9% (Ba+Sr) rich film and for the 6% (Ba+Sr) poor film ranged from 70 to 100 nm and from 30 to 60 nm, respectively. This grain size difference could explain why slightly A-site rich (Ba,Sr)TiO3 films have a larger dielectric constant than A-site poor films.

Selective oxidation of n-butane to maleic anhydride under oxygen-deficient conditions over V-P-O mixed oxides

NARCIS (Netherlands)

Bosch, H.; Bruggink, A.A.; Ross, J.R.H.

1987-01-01

The selective oxidation of n-butane to maleic anhydride over V-P-O mixed oxides was studied under oxygen deficient conditions. The mixed oxides were prepared with P/V atomic ratios ranging from 0.7 to 1.0. Catalysts with P/V <1.0 did not show any selectivity to maleic anhydride formation, regardless

Numerical Investigation of Mixing Characteristics in Cavity Flow at Various Aspect Ratios

Energy Technology Data Exchange (ETDEWEB)

Shin, Myung Seob [Dongyang Mirae University, Seoul (Korea, Republic of); Yang, Seung Deok; Yoon, Joon Yong [Hanyang University, Seoul (Korea, Republic of)

2015-01-15

This study numerically examined the mixing characteristics of rectangular cavity flows by using the hybrid lattice Boltzmann method (HLBM) applied to the finite difference method (FDM). Multi-relaxation time was used along with a passive scalar method which assumes that two substances have the same mass and that there is no interaction. First, we studied numerical results such as the stream function, position of vortices, and velocity profile for a square cavity and rectangular cavity with an aspect ratio of 2. The data were compared with previous numerical results that have been proven to be reliable. We also studied the mixing characteristics of a rectangular cavity flow such as the concentration profile and average Sherwood number at various Pe numbers and aspect ratios.

Atomic Layer Deposition of Al2O3-Ga2O3 Alloy Coatings for Li[Ni0.5Mn0.3Co0.2]O2 Cathode to Improve Rate Performance in Li-Ion Battery.

Science.gov (United States)

Laskar, Masihhur R; Jackson, David H K; Guan, Yingxin; Xu, Shenzhen; Fang, Shuyu; Dreibelbis, Mark; Mahanthappa, Mahesh K; Morgan, Dane; Hamers, Robert J; Kuech, Thomas F

2016-04-27

Metal oxide coatings can improve the electrochemical stability of cathodes and hence, their cycle-life in rechargeable batteries. However, such coatings often impose an additional electrical and ionic transport resistance to cathode surfaces leading to poor charge-discharge capacity at high C-rates. Here, a mixed oxide (Al2O3)1-x(Ga2O3)x alloy coating, prepared via atomic layer deposition (ALD), on Li[Ni0.5Mn0.3Co0.2]O2 (NMC) cathodes is developed that has increased electron conductivity and demonstrated an improved rate performance in comparison to uncoated NMC. A "co-pulsing" ALD technique was used which allows intimate and controlled ternary mixing of deposited film to obtain nanometer-thick mixed oxide coatings. Co-pulsing allows for independent control over film composition and thickness in contrast to separate sequential pulsing of the metal sources. (Al2O3)1-x(Ga2O3)x alloy coatings were demonstrated to improve the cycle life of the battery. Cycle tests show that increasing Al-content in alloy coatings increases capacity retention; whereas a mixture of compositions near (Al2O3)0.5(Ga2O3)0.5 was found to produce the optimal rate performance.

A novel method for stoichiometric reduction of (U{sub 3}O{sub 8},PuO{sub 2}) and its controlled oxidation using microwave

Energy Technology Data Exchange (ETDEWEB)

Singh, G., E-mail: gitendars@barctara.gov.in [Advanced Fuel Fabrication Facility (AFFF), Bhabha Atomic Research Centre, Tarapur, 401 502 (India); Kumar, Pradeep [Integrated Fuel Fabrication Facility, Bhabha Atomic Research Centre, Mumbai, 400 085 (India); Aher, S.; Purohit, P.; Khot, P.M. [Advanced Fuel Fabrication Facility (AFFF), Bhabha Atomic Research Centre, Tarapur, 401 502 (India); Prakash, Amrit [Radio-Metallurgy Division, Bhabha Atomic Research Centre, Mumbai, 400 085 (India); Das, D.K.; Behere, P.G.; Afzal, Mohd [Advanced Fuel Fabrication Facility (AFFF), Bhabha Atomic Research Centre, Tarapur, 401 502 (India)

2016-10-15

We report a process for stoichiometric reduction of U{sub 3}O{sub 8} and (U{sub 3}O{sub 8},PuO{sub 2}) mixed oxide powders using an indigenously developed 2.4 GHz microwave processing system. The process parameters were optimized by interpreting reduction kinetic curves at a temperature which is 150 °C lower than the conventional reduction. The process improved the sinterability of the powder which was evaluated in terms of average particle size, BET specific surface area and bulk density. A quick method for controlled oxidation of the reduced powder to incorporate a controlled amount of hyper-stoichiometry was demonstrated by modifying the same reduction process. The percent reduction was measured experimentally using O:(U + Pu) ratio. The X-ray diffraction analysis confirmed the various phases present. The process is novel considering shorter processing cycle, lower temperature processing, improved powder properties, energy efficiency and cost effectiveness. - Highlights: • A process for stoichiometric reduction of (U{sub 3}O{sub 8},PuO{sub 2}) was demonstrated using 2.4 GHz microwave. • A simple and quick method for obtaining controlled hyper-stoichiometry in the reduced powder was successfully demonstrated. • The process is novel relative to conventional methods in terms of time and energy economy and sinter-activity.

Parameterizing radiative transfer to convert MAX-DOAS dSCDs into near-surface box-averaged mixing ratios

Directory of Open Access Journals (Sweden)

R. Sinreich

2013-06-01

Full Text Available We present a novel parameterization method to convert multi-axis differential optical absorption spectroscopy (MAX-DOAS differential slant column densities (dSCDs into near-surface box-averaged volume mixing ratios. The approach is applicable inside the planetary boundary layer under conditions with significant aerosol load, and builds on the increased sensitivity of MAX-DOAS near the instrument altitude. It parameterizes radiative transfer model calculations and significantly reduces the computational effort, while retrieving ~ 1 degree of freedom. The biggest benefit of this method is that the retrieval of an aerosol profile, which usually is necessary for deriving a trace gas concentration from MAX-DOAS dSCDs, is not needed. The method is applied to NO2 MAX-DOAS dSCDs recorded during the Mexico City Metropolitan Area 2006 (MCMA-2006 measurement campaign. The retrieved volume mixing ratios of two elevation angles (1° and 3° are compared to volume mixing ratios measured by two long-path (LP-DOAS instruments located at the same site. Measurements are found to agree well during times when vertical mixing is expected to be strong. However, inhomogeneities in the air mass above Mexico City can be detected by exploiting the different horizontal and vertical dimensions probed by the MAX-DOAS and LP-DOAS instruments. In particular, a vertical gradient in NO2 close to the ground can be observed in the afternoon, and is attributed to reduced mixing coupled with near-surface emission inside street canyons. The existence of a vertical gradient in the lower 250 m during parts of the day shows the general challenge of sampling the boundary layer in a representative way, and emphasizes the need of vertically resolved measurements.

Electronic interaction in an outer-sphere mixed-valence double salt: a polarized neutron diffraction study of K(3)(MnO(4))(2).

Science.gov (United States)

Cannon, Roderick D; Jayasooriya, Upali A; Tilford, Claire; Anson, Christopher E; Sowrey, Frank E; Rosseinsky, David R; Stride, John A; Tasset, Francis; Ressouche, Eric; White, Ross P; Ballou, Rafik

2004-11-01

The mixed-valence double salt K(3)(MnO(4))(2) crystallizes in space group P2(1)/m with Z = 2. The manganese centers Mn1 and Mn2 constitute discrete "permanganate", [Mn(VII)O(4)](-), and "manganate", [Mn(VI)O(4)](2-), ions, respectively. There is a spin-ordering transition to an antiferromagnetic state at ca. T = 5 K. The spin-density distribution in the paramagnetic phase at T = 10 K has been determined by polarized neutron diffraction, confirming that unpaired spin is largely confined to the nominal manganate ion Mn2. Through use of both Fourier refinement and maximum entropy methods, the spin on Mn1 is estimated as 1.75 +/- 1% of one unpaired electron with an upper limit of 2.5%.

A Study on Production of Carbon Nanotubes by CH4 Decomposition over LaNiO3, La4Ni3O10, La3Ni2O7 and La2NiO4

Institute of Scientific and Technical Information of China (English)

无

2001-01-01

Carbon nanotubes (CNTs) of narrow size distribution can be abundantly produced in the catalytic decomposition of CH4 over pre-reduced LaNiO3, La4Ni3O10, La3Ni2O7 and La2NiO4.The CNTs obtained were characterized by means of transmission electron microscopy (TEM).Thermal oxidation of CNTs in air was monitored thermogravimetrically (TG). The resultsrevealed that a lower La/Ni ratio of the catalysts would lead to a wider diameter distribution and a higher degree of graphitic nature.

Liquidus Temperature of SrO-Al2O3-SiO2 Glass-Forming Compositions

DEFF Research Database (Denmark)

Abel, Brett M.; Morgan, James M.; Mauro, John C.

2013-01-01

. In the composition range of interest for industrial glasses, Tliq tends to decrease with increasing strontium-to-alumina ratio. We find that cristobalite, mullite, and slawsonite are the dominant devitrification phases for the compositions with high SiO2, SiO2+Al2O3, and SrO contents, respectively. By comparison...... with the phase diagrams for CaO-Al2O3-SiO2 and MgO-Al2O3-SiO2 systems, we have found that for the highest [RO]/[Al2O3] ratios, Tliq exhibits a minimum value for R = Ca. Based on the phase diagram established here, the composition of glass materials, for example, for liquid crystal display substrates, belonging...... to the SrO-Al2O3-SiO2 family may be designed with a more exact control of the glass-forming ability by avoiding the regions of high liquidus temperature....

Characterization studies of β-Ti3O5 and λ-Ti3O5 nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Tasca, Kelin Regina; Giles, Carlos, E-mail: kelinregina@gmail.com [Universidade Estadual de Campinas (UNICAMP), SP (Brazil). Instituto de Fisica Gleb Wataghin

2016-07-01

Full text: Recently, a new phase of Ti3O5 with properties of a metallic conductor and thermodynamically stable at room temperature due to nanoscale effects was reported. The new phase, namely λ-Ti3O5, presents a monoclinic structure with characteristics of a near-metallic conductor. At room temperature a photoreversible phase transition between λ-Ti3O5 and the conventional semiconductor phase, β-Ti3O5, is induced by light excitation. The thermodynamic analysis suggests that the photoinduced metal-semiconductor phase transition is a result of a transition from λ-Ti3O5, a metastable phase thermodynamically trapped at a local energy-minimum state, to a truly stable phase β-Ti3O5, by irradiation of a pulsed laser light. The direction of the photoinduced phase transition can be controlled by adjusting the excitation fluence at a constant wavelength, or changing the wavelength. In both cases, the fluence and the wavelength have well defined threshold values.Due to the existence of a photoinduced phase transition and to environmentally benign characteristics this material is a strong candidate for high density optical storage media. In the present work Ti3O5 nanoparticles were synthesized by sintering 30 nm commercial anatase-TiO{sub 2} nanoparticles in hydrogen flux at 1200 deg C during 2 h. The sample was characterized by x-ray powder diffractometry (XRD) and the results showed a mixed phase of λ-Ti3O5 and β-Ti3O5. With the purpose to perform future time-resolved XRD experiments, a thin film of the mixed Ti3O5 sample was prepared in a FTO glass substrate and heated up to 450 deg C. From this process a thin film of λ-Ti3O5 nanoparticles with a small amount of rutile-TiO2 resulted. These results are different from the so far published work and can contribute to the comprehension of this phenomena. To better understand this phase transition XRD as a function of temperature and under the influence of laser incidence will be presented. (author)

Characterization studies of β-Ti3O5 and λ-Ti3O5 nanoparticles

International Nuclear Information System (INIS)

Tasca, Kelin Regina; Giles, Carlos

2016-01-01

Full text: Recently, a new phase of Ti3O5 with properties of a metallic conductor and thermodynamically stable at room temperature due to nanoscale effects was reported. The new phase, namely λ-Ti3O5, presents a monoclinic structure with characteristics of a near-metallic conductor. At room temperature a photoreversible phase transition between λ-Ti3O5 and the conventional semiconductor phase, β-Ti3O5, is induced by light excitation. The thermodynamic analysis suggests that the photoinduced metal-semiconductor phase transition is a result of a transition from λ-Ti3O5, a metastable phase thermodynamically trapped at a local energy-minimum state, to a truly stable phase β-Ti3O5, by irradiation of a pulsed laser light. The direction of the photoinduced phase transition can be controlled by adjusting the excitation fluence at a constant wavelength, or changing the wavelength. In both cases, the fluence and the wavelength have well defined threshold values.Due to the existence of a photoinduced phase transition and to environmentally benign characteristics this material is a strong candidate for high density optical storage media. In the present work Ti3O5 nanoparticles were synthesized by sintering 30 nm commercial anatase-TiO 2 nanoparticles in hydrogen flux at 1200 deg C during 2 h. The sample was characterized by x-ray powder diffractometry (XRD) and the results showed a mixed phase of λ-Ti3O5 and β-Ti3O5. With the purpose to perform future time-resolved XRD experiments, a thin film of the mixed Ti3O5 sample was prepared in a FTO glass substrate and heated up to 450 deg C. From this process a thin film of λ-Ti3O5 nanoparticles with a small amount of rutile-TiO2 resulted. These results are different from the so far published work and can contribute to the comprehension of this phenomena. To better understand this phase transition XRD as a function of temperature and under the influence of laser incidence will be presented. (author)

The influence of Uranium-Thorium ratio and heating time during gelation using as a CCl4(NH3) on the Gel quality

International Nuclear Information System (INIS)

Indra-Suryawan; Sukarsono, R; Setyo-Sulardi

1996-01-01

Gel has been prepared from a uranium-thorium sol using CCI 4 (NH 3 ) as a gelling medium. The uranium-thorium ratio and the heating time during gelation have been chosen as variables. The sol was prepared by mixing Th(NO 3 ) 4 and UO 2 (NO 3 ) 2 solutions, heating the solution at 95 o C and adding NH 4 OH solution drop by drop until colloidal particles were formed. Sol was then fed into a gelation column containing CCI 4 (NH 3 ), where the sol was transformed into gel. A good gel has properties such as sphere in shape and elastic which it will not crack when it is dropped from 2 metres height. The experimental work resulted a good gel when the percentage of uranium was about 15 - 25 % at heating time of 40 - 50 minutes

Tequila authenticity assessment by headspace SPME-HRGC-IRMS analysis of 13C/12C and 18O/16O ratios of ethanol.

Science.gov (United States)

Aguilar-Cisneros, Blanca O; López, Mercedes G; Richling, Elke; Heckel, Frank; Schreier, Peter

2002-12-18

By use of headspace SPME sampling and a PLOT column, on-line capillary gas chromatography-isotope ratio mass spectrometry was employed in the combustion (C) and the pyrolysis (P) modes (HRGC-C/P-IRMS) to determine the delta(13)C(VPDB) and delta(18)O(VSMOW) values of ethanol in authentic (n = 14) and commercial tequila samples (n = 15) as well as a number of other spirits (n = 23). Whereas with delta(13)C(VPDB) values ranging from -12.1 to -13.2 per thousand and from -12.5 to -14.8 per thousand similar variations were found for 100% agave and mixed tequilas, respectively, the delta(18)O(VSMOW) data differed slightly within these categories: ranges from +22.1 to +22.8 per thousand and +20.8 to +21.7 per thousand were determined for both the authentic 100% agave and mixed products, respectively. The data recorded for commercial tequilas were less homogeneous; delta(13)C(VPDB) data from -10.6 to -13.9 per thousand and delta(18)O(VSMOW) values from +15.5 to +22.7 per thousand were determined in tequilas of both categories. Owing to overlapping data, attempts to differentiate between white, rested, and aged tequilas within each of the two categories failed. In addition, discrimination of tequila samples from other spirits by means of delta(13)C(VPDB) and delta(18)O(VSMOW) data of ethanol was restricted to the products originating from C(3) as well as C(4)/CAM raw materials.

Reactions of 11C recoil atoms in the systems H2O-NH3, H2O-CH4 and NH3-CH4

International Nuclear Information System (INIS)

Nebeling, B.

1988-11-01

In this study the chemical reactions of recoil carbon 11 in the binary gas mixtures H 2 O-NH 3 , H 2 O-CH 4 and NH 3 -CH 4 in different mixing ratios as well as in solid H 2 O and in a solid H 2 O-NH 3 mixture were analyzed in dependence of the dose. The analyses were to serve e.g. the simulation of chemical processes caused by solar wind, solar radiation and cosmic radiation in the coma and core of comets. They were to give further information about the role of the most important biogeneous element carbon, i.e. carbon, in the chemical evolution of the solar system. Besides the actual high energy processes resulting in the so-called primary products, also the radiation-chemical changes of the primary products were also observed in a wide range of dosing. The generation of the energetic 11 C atoms took place according to the target composition by the nuclear reactions 14 N(p,α) 11 C, 12 C( 3 He,α) 11 C or the 16 O(p,αpn) 11 C reaction. The identification of the products marked with 11 C was carried out by means of radio gas chromatography or radio liquid chromatography (HPLC). (orig./RB) [de

Investigation of Atwood ratio influence on turbulent mixing transition of a shock-driven variable density flow after reshock

Science.gov (United States)

Mohaghar, Mohammad; Carter, John; Pathikonda, Gokul; Ranjan, Devesh

2017-11-01

The current study experimentally investigates the influence of the initial Atwood ratio (At) on the evolution of Richtmyer-Meshkov instability at the Georgia Tech Shock Tube and Advanced Mixing Laboratory. Two Atwood numbers (At =0.22 and 0.67) are studied, which correspond to the gas combinations of nitrogen seeded with acetone vapor (light) over carbon dioxide (heavy) and same light gas over sulfur hexafluoride (heavy) respectively. A perturbed, multi-mode, inclined interface (with an amplitude to wavelength ratio of 0.088) is impulsively accelerated by the incident shock traveling vertically from light to heavy gas with a Mach number 1.55. The effect of Atwood ratio on turbulent mixing transition after reshock at the same non-dimensional times between the two cases is examined through ensemble-averaged turbulence statistics from simultaneous planar laser induced uorescence (PLIF) and particle image velocimetry (PIV) measurements. Preliminary studies over the smaller Atwood number indicates that turbulent mixing transition criteria can be satisfied after reshock. This work was supported by the National Science Foundation CAREER Award No. 1451994.

A Simple Method for the Preparation of ZnO Prickly Spheres

Institute of Scientific and Technical Information of China (English)