Evaluation of the exothermicity of the chemi-ionization reaction Sm + O → SmO+ + e−

International Nuclear Information System (INIS)

Cox, Richard M; Kim, JungSoo; Armentrout, P. B.; Bartlett, Joshua; VanGundy, Robert A.; Heaven, Michael C.; Ard, Shaun G.; Shuman, Nicholas S.; Viggiano, Albert A.; Melko, Joshua J.

2015-01-01

The exothermicity of the chemi-ionization reaction Sm + O → SmO + + e − has been re-evaluated through the combination of several experimental methods. The thermal reactivity (300–650 K) of Sm + and SmO + with a range of species measured using a selected ion flow tube-mass spectrometer apparatus is reported and provides limits for the bond strength of SmO + , 5.661 eV ≤ D 0 (Sm + -O) ≤ 6.500 eV. A more precise value is measured to be 5.72 5 ± 0.07 eV, bracketed by the observed reactivity of Sm + and SmO + with several species using a guided ion beam tandem mass spectrometer (GIBMS). Combined with the established Sm ionization energy (IE), this value indicates an exothermicity of the title reaction of 0.08 ± 0.07 eV, ∼0.2 eV smaller than previous determinations. In addition, the ionization energy of SmO has been measured by resonantly enhanced two-photon ionization and pulsed-field ionization zero kinetic energy photoelectron spectroscopy to be 5.7427 ± 0.0006 eV, significantly higher than the literature value. Combined with literature bond energies of SmO, this value indicates an exothermicity of the title reaction of 0.14 ± 0.17 eV, independent from and in agreement with the GIBMS result presented here. The evaluated thermochemistry also suggests that D 0 (SmO) = 5.83 ± 0.07 eV, consistent with but more precise than the literature values. Implications of these results for interpretation of chemical release experiments in the thermosphere are discussed

Carbon Domains on MoS2/TiO2 System via Catalytic Acetylene Oligomerization: Synthesis, Structure, and Surface Properties

Directory of Open Access Journals (Sweden)

Sara Cravanzola

2017-11-01

Full Text Available Carbon domains have been obtained at the surface of a MoS2/TiO2 (Evonik, P25 system via oligomerization and cyclotrimerization reactions involved in the interaction of the photoactive material with acetylene. Firstly, MoS2 nanosheets have been synthesized at the surface of TiO2, via sulfidation of a molybdenum oxide precursor with H2S (bottom-up method. Secondly, the morphology and the structure, the optical and the vibrational properties of the obtained materials, for each step of the synthesis procedure, have been investigated by microscopy and spectroscopy methods. In particular, transmission electron microscopy images provide a simple tool to highlight the effectiveness of the sulfidation process, thus showing 1L, 2L, and stacked MoS2 nanosheets anchored to the surface of TiO2 nanoparticles. Lastly, in-situ FTIR spectroscopy investigation gives insights into the nature of the oligomerized species, showing that the formation of both polyenic and aromatic systems can be taken into account, being their formation promoted by both Ti and Mo catalytic sites. This finding gives an opportunity for the assembly of extended polyenic, polyaromatic, or mixed domains firmly attached at the surface of photoactive materials. The presented approach, somehow different from the carbon adding or doping processes of TiO2, is of potential interest for the advanced green chemistry and energy conversion/transport applications.

XPS-UPS, ISS characterization studies and the effect of Pt and K addition on the catalytic properties of MoO{sub 2-x}(OH){sub y} deposited on TiO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Al-Kandari, H. [Public Authority of Applied Education and Training (Kuwait); Mohamed, A.M.; Al-Kharafi, F. [Kuwait University, Department of Chemistry, P.O. Box 5969, Safat 13060 (Kuwait); Katrib, A., E-mail: ali.katrib@ku.edu.kw [Kuwait University, Department of Chemistry, P.O. Box 5969, Safat 13060 (Kuwait)

2011-11-15

Highlights: {yields} Surface electronic structure-catalytic activity correlation is presented in this research work. {yields} In situ characterization by XPS-UPS and ISS techniques were employed at the same experimental conditions applied for catalytic reactions. {yields} Catalytic reactions of Mo deposited on titanium oxide for the isomerization and hydrogenation reactions using 1-hexene and n-hexane were studied. {yields} The bifunctional properties of the molybdenum dioxide phase were modified by the addition of potassium. - Abstract: Characterization by XPS-UPS, ISS surface techniques of MoO{sub 3}/TiO{sub 2} catalysts before and after addition of Pt (PtMo) 2.5% by weight of MoO{sub 3} and potassium (KMo) enabled to identify different chemical species present on the outermost surface layer at different reduction temperatures. Catalytic activities of these systems using 1-hexene and n-hexane reactants were studied. Correlation between catalytic activity and surface electronic structure enabled us to identify the chemical species, active site(s), responsible for specific catalytic reaction(s).

Effect of hydrogen on the growth and morphology of single wall carbon nanotubes synthesized on a Fe-Mo/MgO catalytic system

Energy Technology Data Exchange (ETDEWEB)

Biris, Alexandru R. [National Institute for Research and Development of Isotopic and Molecular Technologies, Cluj Napoca, RO-3400 (Romania)], E-mail: biris@oc1.itim-cj.ro; Li Zhongrui; Dervishi, Enkeleda [Applied Science Department, University of Arkansas at Little Rock, 2801 S. University Ave, Little Rock, AR 72204 (United States); Nanotechnology Center, University of Arkansas at Little Rock, 2801 S. University Ave, Little Rock, AR 72204 (United States); Lupu, Dan [National Institute for Research and Development of Isotopic and Molecular Technologies, Cluj Napoca, RO-3400 (Romania); Xu Yang; Saini, Viney [Applied Science Department, University of Arkansas at Little Rock, 2801 S. University Ave, Little Rock, AR 72204 (United States); Nanotechnology Center, University of Arkansas at Little Rock, 2801 S. University Ave, Little Rock, AR 72204 (United States); Watanabe, Fumiya [Nanotechnology Center, University of Arkansas at Little Rock, 2801 S. University Ave, Little Rock, AR 72204 (United States); Biris, Alexandru S. [Applied Science Department, University of Arkansas at Little Rock, 2801 S. University Ave, Little Rock, AR 72204 (United States); Nanotechnology Center, University of Arkansas at Little Rock, 2801 S. University Ave, Little Rock, AR 72204 (United States)], E-mail: asbiris@ualr.edu

2008-04-21

Single wall carbon nanotubes were synthesized from thermal pyrolysis of methane on a Fe-Mo/MgO catalyst by radio frequency catalytic chemical vapor deposition (RF-CVD) using argon as a carrier gas. Controlled amounts of hydrogen (H{sub 2}/CH{sub 4}=0-1 v/v) were introduced in separate experiments along with the carbon source. The properties and morphology of the synthesized single wall carbon nanotubes were monitored by transmission electron microscopy, Raman scattering, and thermogravimetric analysis. The nanotubes with the highest crystallinity were obtained with H{sub 2}/CH{sub 4}=0.6. By monitoring the Radial Breathing Modes present in the Raman spectra of the single-wall carbon nanotube samples, the variation of the structural and morphological properties of the carbon nanotubes with the flow level of hydrogen, reflect changes of the catalyst systems induced by the presence of hydrogen.

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

Ternary system of Na2MoO4-Cs2MoO4-MoO3

International Nuclear Information System (INIS)

Zueva, V.P.; Shabanova, A.N.; Drobasheva, T.I.

1982-01-01

Using the methods of thermal analysis interaction of components in ternary system Na 2 MoO 4 -Cs 2 MoO 4 -MoO 3 has been studied. Crystallization surface consists of nine fields belonging to initial components and compounds of lateral sides. Triangulation of the system is carried out and the character of nonvariant points is clarified, the temperature of 360 deg C corresponds to low-melting eutectics

Phase formation in Na2MoO4 - MgMoO4 - Cr2(MoO4)3 system

International Nuclear Information System (INIS)

Kotova, I.Yu.; Kozhevnikova, N.M.

1998-01-01

Interaction within Na 2 MoO 4 - MgMoO 4 - Cr 2 (MoO 4 ) 3 ternary system is studied by X ray phase and DTA methods. State diagram of NaCr(MoO 4 ) 2 - MgMoO 4 section is plotted. Production of ternary molybdates of Na 1-x Mg 1-x Cr 1+x (MoO 4 ) 3 , where 0 ≤ x ≤ 0.3, and NaMg 3 Cr(MoO 4 ) 5 composition is ascertained [ru

Tune color of single-phase LiGd(MoO4)2-X(WO4)X: Sm3+, Tb3+ via adjusting the proportion of matrix and energy transfer to create white-light phosphor

Science.gov (United States)

Wu, Hongyue; Yang, Junfeng; Wang, Xiaoxue; Gan, Shucai; Li, Linlin

2018-03-01

A series of LiGd(MO4)2: Sm3+, Tb3+ (M = Mo, W) phosphors was prepared by a conventional solid state reaction method. Powder X-Ray diffraction (XRD) analysis reveals that the compounds are of the same structure type. Their luminescent properties have been studied. The optimal doping concentrations are 8% for Sm3+ and 18% for Tb3+ in the LiGd(MoO4)2 host. Sm3+ and Tb3+ have different sensitivity to the Mo/W ratio. For LiGd(MoO4)2-X(WO4)X: Sm3+ (X = 0, 0.4, 0.8, 1.2, 1.6, 2.0), the strongest emission intensity is 1.766 times than that of the weakest, while 171 times for LiGd(MoO4)2-X(WO4)X: Tb3+. The experimental results show that Mo/W ratio strong influences on the properties of LiGd(MoO4)2-X(WO4)X: Tb3+. With the increasing of WO42- groups concentration, the shape of characteristic excitation peaks of Tb3+ is almost the same and the excitation intensity gradually increase. Moreover, the energy transfer from Tb3+ to Sm3+ has been realized in the co-doped phosphors. The experimental analysis and theoretical calculations reveal that the quadrupole-quadrupole interaction is the dominant mechanism for the Tb3+→Sm3+ energy transfer. Therefore, luminous intensity can be adjusted by different sensitivities to matrix composition and energy transfer from Tb3+→Sm3+. By this tuning color method, white-light-emitting phosphor has been prepared. The excitation wavelength is 378 nm, and this indicates that the white-light-emitting phosphor could be pumped by near-UV light.

Hydrothermal Synthesis of MoO2 and Supported MoO2 Cata-lysts for Oxidative Desulfurization of Dibenzothiophene

Institute of Scientific and Technical Information of China (English)

Wang Danhong; Zhang Jianyong; Liu Ni; Zhao Xin; Zhang Minghui

2014-01-01

A novel method for obtaining spherical MoO2 nanoparticles and SiO2-Al2O3 supported MoO2 by hydrothermal reduction of Mo (VI) species was studied. The obtained MoO2 catalysts show very high catalytic activity in the oxidative desulfurization (ODS) process. The effect of hydrothermal temperature and crystallization temperature on ODS activity was investigated. The ODS activity of supported MoO2 catalysts with various MoO2 contents were also investigated. The mecha-nism for formation of MoO2 involving oxalic acid was proposed.

LaMn1-xFe xO3 and LaMn0.1-xFe0.90Mo x O3 perovskites: synthesis, characterization and catalytic activity in H2O2 reactions

Directory of Open Access Journals (Sweden)

Fabiano Magalhães

2008-09-01

Full Text Available In this work two perovskites were prepared: LaMn1-xFe xO3, and LaMn0.1-x Fe0.90Mo xO3. XRD and Mössbauer spectroscopy suggest the formation of pure phase perovskite with the incorporation of Fe and Mo in the structure. The catalytic activity of these materials was studied in two reactions with H2O2: the decomposition to O2, and the oxidation of the model organic contaminant methylene blue. The perovskite composition strongly affects the catalytic activity, while Fe decreases the H2O2 decomposition Mo strongly improves dye oxidation.

Preparation, Characterization and Catalytic Activity of Nickel Molybdate (NiMoO4 Nanoparticles

Directory of Open Access Journals (Sweden)

Hicham Oudghiri-Hassani

2018-01-01

Full Text Available Nickel molybdate (NiMoO4 nanoparticles were synthesized via calcination of an oxalate complex in static air at 500 °C. The oxalate complex was analyzed by thermal gravimetric analysis (TGA and Fourier transform infrared spectroscopy (FTIR. The as-synthesized nickel molybdate was characterized by Brunauer–Emmett–Teller technique (BET, X-ray diffraction (XRD, and transmission electron microscopy (TEM and its catalytic efficiency was tested in the reduction reaction of the three-nitrophenol isomers. The nickel molybdate displays a very high activity in the catalytic reduction of the nitro functional group to an amino. The reduction progress was controlled using Ultraviolet-Visible (UV-Vis absorption.

Phase relations in the M2MoO4 - Ag2MoO4 - Hf(MoO4)2 (M=Li, Na) systems

International Nuclear Information System (INIS)

Bazarova, Zh.G.; Bazarov, B.G.; Balsanova, L.V.

2002-01-01

The M 2 MoO 4 - Ag 2 MoO 4 - Hf(MoO 4 ) 2 (M=Li, Na) systems were studied by X-ray diffraction and differential thermal analyses in the subsolidus area (450 - 500 Deg C) for the first time. The formation of the binary compound with the variable composition Li 4-x Hf 1+0.2x (MoO 4 ) 4 (0 ≤ x ≤ 0.6) in the Li 2 MoO 4 - Hf(MoO 4 ) 2 system and the ternary molybdates Li 4 Ag 2 Hf(MoO 4 ) 5 (S 1 ) and Na 2 Ag 2 Hf(MoO 4 ) 4 (S 2 ) was established and the thermal characteristics of the prepared compounds were examined. The new binary molybdate Ag 2 Hf(MoO 4 ) 3 was prepared by the reaction between Ag 2 MoO 4 and Hf(MoO 4 ) 2 [ru

Correlation between the nanocrystalline Sm(Fe,Mo){sub 12} and its out of equilibrium phase Sm(Fe,Mo){sub 10}

Energy Technology Data Exchange (ETDEWEB)

Khazzan, S. [CMTR, ICMPE, UMR7182, CNRS - Université Paris Est, 2-8 rue Henri Dunant, F-94320 Thiais (France); Laboratoire Matériaux Organisation et Propriétés, Faculté des Sciences de Tunis, Université de Tunis El Manar, 2092 Tunis (Tunisia); Bessais, L., E-mail: bessais@glvt.cnrs.fr [CMTR, ICMPE, UMR7182, CNRS - Université Paris Est, 2-8 rue Henri Dunant, F-94320 Thiais (France); Van Tendeloo, G. [EMAT, University of Antwerp, B-2020 Antwerp (Belgium); Mliki, N. [Laboratoire Matériaux Organisation et Propriétés, Faculté des Sciences de Tunis, Université de Tunis El Manar, 2092 Tunis (Tunisia)

2014-08-01

Nanostructured Sm–Fe–Mo semi-hard magnetic material exhibiting enhanced magnetic properties can be produced by ball milling followed by recrystallization. Milled samples were annealed for 30 min in a vacuum at different temperatures (T{sub A}) between 700 and 1190 °C. The effects of heat treatment and Mo content on structural and magnetic property changes have been investigated by means of X-ray diffraction using the Rietveld method, transmission electron microscopy and magnetic measurements. For samples annealed at T{sub A}>900°C the tetragonal ThMn{sub 12}-type structure is identified, while for 700Sm(Fe{sub 1−x}Mo{sub x}){sub 10}, correlated with structural transformation towards its equilibrium derivative I4/mmm Sm(Fe{sub 1−x}Mo{sub x}){sub 12}. A maximum of the coercive field H{sub C} (H{sub C}>5kOe) has been observed for the new hexagonal P6/mmm phase suggesting that nanocrystalline Sm(Fe,Mo){sub 10}, is a semi-hard material, and is potential candidate for magnetic recording. - Highlights: • A study of the structure and magnetic properties of SmFeMo compound. • A new out of equilibrium P6/mmm-type structure was found. • Correlation between the 1/12 phase and its out of equilibrium 1/10 phase.

Comparative study on catalytic behavior of polynuclear Mg-Mo-complex and FeMo-co-factor of nitrogenase in reactions with C2H2, N2 and CO

International Nuclear Information System (INIS)

Bardina, N.V.; Bazhenova, T.A.; Petrova, G.N.; Shilova, A.K.; Shilov, A.E.

2006-01-01

Catalytic reduction kinetics of C 2 H 2 in the presence of the Mg-Mo-cluster {[Mg 2 Mo 8 O 22 (MeO) 6 (MeOH) 4 ] 2- [Mg(MeOH) 6 ] 2+ }·6MeOH 1 is studied. Several interdependent coordinating centers are active in reference to substrates and inhibitors in the polynuclear Mg-Mo-complex, as in the reduced by europium amalgam (μ 6 -N)MoFe 7 S 9 ·homocitrate (FeMoco, 2). Comparison of regularities in reduction mechanism of C 2 H 2 , N 2 and CO with the participation of synthetic polynuclear complex 1 and natural cluster 2 is conducted. Regularities of the studied reactions in the systems involving natural catalytic cluster FeMoco and the synthetic Mg-Mo-complex modelling of its effect are noted to be similar. The main variations the systems show as regards to the reaction with molecular nitrogen [ru

Structural/surface characterization and catalytic evaluation of rare-earth (Y, Sm and La) doped ceria composite oxides for CH{sub 3}SH catalytic decomposition

Energy Technology Data Exchange (ETDEWEB)

He, Dedong; Chen, Dingkai; Hao, Husheng; Yu, Jie; Liu, Jiangping; Lu, Jichang; Liu, Feng [Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming, 650500 (China); Wan, Gengping [Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming, 650500 (China); Research Center for Analysis and Measurement, Hainan University, Haikou, 570228 (China); He, Sufang [Research Center for Analysis and Measurement, Kunming University of Science and Technology, Kunming, 650093 (China); Luo, Yongming, E-mail: environcatalysis222@yahoo.com [Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming, 650500 (China)

2016-12-30

Highlights: • Ce{sub 0.75}RE{sub 0.25}O{sub 2-δ} (RE = Y, Sm and La) were synthesized by citrate complexation method. • Ce{sub 0.75}Y{sub 0.25}O{sub 2-δ} exhibited the best stability for the decomposition of CH{sub 3}SH. • Cation radius played a key role in determining structure and surface characteristics. • Catalytic behavior depended on synergistic role of oxygen vacancies and basic sites. • Ce{sub 2}S{sub 3} accumulation on the surface was responsible for the deactivation of catalyst. - Abstract: A series of rare earth (Y, Sm and La) doped ceria composite oxides and pure CeO{sub 2} were synthesized and evaluated by conducting CH{sub 3}SH catalytic decomposition test. Several characterization studies, including XRD, BET, Raman, H{sub 2}-TPR, XPS, FT-IR, CO{sub 2}-TPD and CH{sub 3}SH-TPD, were undertaken to correlate structural and surface properties of the obtained ceria-based catalysts with their catalytic performance for CH{sub 3}SH decomposition. More oxygen vacancies and increased basic sites exhibited in the rare earth doped ceria catalysts. Y doped ceria sample (Ce{sub 0.75}Y{sub 0.25}O{sub 2-δ}), with a moderate increase in basic sites, contained more oxygen vacancies. More structural defects and active sites could be provided, and a relatively small amount of sulfur would accumulate, which resulted in better catalytic performance. The developed catalyst presented good catalytic behavior with stability very similar to that of typical zeolite-based catalysts reported previously. However, La doped ceria catalyst (Ce{sub 0.75}La{sub 0.25}O{sub 2-δ}) with the highest alkalinity was not the most active one. More sulfur species would be adsorbed and a large amount of cerium sulfide species (Ce{sub 2}S{sub 3}) would accumulate, which caused deactivation of the catalysts. The combined effect of increased oxygen vacancies and alkalinity led to the catalytic stability of Ce{sub 0.75}Sm{sub 0.25}O{sub 2-δ} sample was comparable to that of pure CeO

Phase formation in the K2MoO4-Lu2(MoO4)3-Hf(MoO4)2 system and the structural study of triple molybdate K5LuHf(MoO4)6

International Nuclear Information System (INIS)

Romanova, E.Yu.; Bazarov, B.G.; Tushinova, Yu.L.; Fedorov, K.N.; Bazarova, Zh.G.; Klevtsova, R.F.; Glinskaya, L.A.

2007-01-01

Interactions in the ternary system K 2 MoO 4 -Lu 2 (MoO 4 ) 3 -Hf(MoO 4 ) 2 have been studied by X-ray powder diffraction and differential thermal analysis. A new triple (potassium lutetium hafnium) molybdate with the 5 : 1 : 2 stoichiometry has been found. Monocrystals of this molybdate have been grown. Its X-ray diffraction structure has been refined (an X8 APEX automated diffractometer, MoK α radiation, 1960 F(hkl), R = 0.0166). The trigonal unit cell has the following parameters: a = 10.6536(1) A, c = 37.8434(8) A, V=3719.75(9) A, Z = 6, space group R3-bar c. The mixed 3D framework of the structure is built of Mo tetrahedra sharing corners with two independent (Lu,Hf)O 6 octahedra. Two sorts of potassium atoms occupy large framework voids [ru

Phase equilibria in the CdMoO4-Gd2(MoO4)3 system

International Nuclear Information System (INIS)

Tunik, T.A.; Fedorov, N.F.; Razumovskij, S.N.

1980-01-01

The constitutional diagram of the CdMoO 4 -Cd 2 (MoO 4 ) 3 system has been plotted using statistical and dynamic methods as well as a complex of instrumental analysis procedures. Three major phases have been found to occur in the systems, viz.: CdMoO 4 based solid solutions that crystallize in the range from 0 to 25 mol.percent of Cd 2 (MoO 4 ) 3 and pass in transit the two-phase narrow region becoming then solid solutions having a distorted scheelite structure and existing in concentrations from 40 to 65 mol.% of Cd 2 (MoO 4 ) 3 . The entire range, in which the Cd 2 (MoO 4 ) 3 solid solutions can exist, amounts to less than 5 mol.%. Certain crystallochemical constants of the phases that occur in the system have been determined [ru

Phase formation in the Li2MoO4–K2MoO4–In2(MoO4)3 system and crystal structures of new compounds K3InMo4O15 and LiK2In(MoO4)3

International Nuclear Information System (INIS)

Khal’baeva, Klara M.; Solodovnikov, Sergey F.; Khaikina, Elena G.; Kadyrova, Yuliya M.; Solodovnikova, Zoya A.; Basovich, Olga M.

2012-01-01

XRD study of solid-phase interaction in the Li 2 MoO 4 –K 2 MoO 4 –In 2 (MoO 4 ) 3 system was performed. The boundary K 2 MoO 4 –In 2 (MoO 4 ) 3 system is an non-quasibinary join of the K 2 O–In 2 O 3 –MoO 3 system where a new polymolybdate K 3 InMo 4 O 15 isotypic to K 3 FeMo 4 O 15 was found. In the structure (a=33.2905(8), b=5.8610(1), c=15.8967(4) Å, β=90.725(1)°, sp. gr. C2/c, Z=8, R(F)=0.0407), InO 6 octahedra, Mo 2 O 7 diortho groups and MoO 4 tetrahedra form infinite ribbons {[In(MoO 4 ) 2 (Mo 2 O 7 )] 3− } ∞ along the b-axis. Between the chains, 8- to 10-coordinate potassium cations are located. A subsolidus phase diagram of the Li 2 MoO 4 –K 2 MoO 4 –In 2 (MoO 4 ) 3 system was constructed and a novel triple molybdate LiK 2 In(MoO 4 ) 3 was revealed. Its crystal structure (a=7.0087(2), b=9.2269(3), c=10.1289(3) Å, β=107.401(1)°, sp. gr. P2 1 , Z=2, R(F)=0.0280) contains an open framework of vertex-shared MoO 4 tetrahedra, InO 6 octahedra and LiO 5 tetragonal pyramids with nine- and seven-coordinate potassium ions in the framework channels. - Graphical abstract: Exploring the Li 2 MoO 4 –K 2 MoO 4 –In 2 (MoO 4 ) 3 system showed its partial non-quasibinarity and revealed new compounds K 3 InMo 4 O 15 (isotypic to K 3 FeMo 4 O 15 ) and LiK 2 In(MoO 4 ) 3 which were structurally studied. An open framework of the latter is formed by vertex-shared MoO 4 tetrahedra, InO 6 octahedra and LiO 5 tetragonal pyramids. Highlights: ► Subsolidus phase relations in the Li 2 MoO 4 –K 2 MoO 4 –In 2 (MoO 4 ) 3 system were explored. ► The K 2 MoO 4 –In 2 (MoO 4 ) 3 system is a non-quasibinary join of the K 2 O–In 2 O 3 –MoO 3 system. ► New compounds K 3 InMo 4 O 15 and LiK 2 In(MoO 4 ) 3 were obtained and structurally studied. ► K 3 InMo 4 O 15 is isotypic to K 3 FeMo 4 O 15 and carries bands of InO 6 , MoO 4 and Mo 2 O 7 units. ► An open framework of LiK 2 In(MoO 4 ) 3 is formed by polyhedra MoO 4 , InO 6 and LiO 5 .

Experimental study of magnetocaloric effect in the two-level quantum system KTm(MoO4)2

Science.gov (United States)

Tarasenko, R.; Tkáč, V.; Orendáčová, A.; Orendáč, M.; Valenta, J.; Sechovský, V.; Feher, A.

2018-05-01

KTm(MoO4)2 belongs to the family of binary alkaline rare-earth molybdates. This compound can be considered to be an almost ideal quantum two-level system at low temperatures. Magnetocaloric properties of KTm(MoO4)2 single crystals were investigated using specific heat and magnetization measurement in the magnetic field applied along the easy axis. Large conventional magnetocaloric effect (-ΔSM ≈ 10.3 J/(kg K)) was observed in the magnetic field of 5 T in a relatively wide temperature interval. The isothermal magnetic entropy change of about 8 J/(kgK) has been achieved already for the magnetic field of 2 T. Temperature dependence of the isothermal entropy change under different magnetic fields is in good agreement with theoretical predictions for a quantum two-level system with Δ ≈ 2.82 cm-1. Investigation of magnetocaloric properties of KTm(MoO4)2 suggests that the studied system can be considered as a good material for magnetic cooling at low temperatures.

Cu4Pr6(MoO4)11-Pr2(MoO4)3 system

International Nuclear Information System (INIS)

Arzumanyan, G.A.

1982-01-01

Existence boundaries and Dalton compositions (CuPr(MoO 4 ) 2 , CuPr 3 (MoO 4 ) 5 ) of solid solutions that in the mojority are of shcheelite dsitored structure have been determined in the Cu 4 Pr 6 (MoO 4 ) 11 -Pr 2 (MoO 4 ) 3 system. It has been revealed that regions of homogeneity near the CuPr(MoO 4 ) 2 composition have a horseshoeshaped profile

Labelling of MoAb with 153SmH1ETA: Preliminary results

International Nuclear Information System (INIS)

Ferro-Flores, G.; De, F.; Ramirez, M.; Pedraza-Lopez, M.; Tendilla, J.I.; Melendez-Alafort, L.; Murphy, C.A.

2001-01-01

A method to label MoAb with Sm-153 using 1,5,9,13-tetraazacyclohexadecane N,N',N'',N''' tetraacetic acid (H 4 ETA) as a bifunctional chelator was developed. H 4 ETA and SmH 1 ETA were synthesized in our laboratory and characterized by IR spectroscopy, TGA (thermogravimetric analysis), SEM (Scattering Electronic Microscopy), EDAX (Elemental Dispersion Analysis by X-rays) and EPR (Electron Paramagnetic Resonance) at 6 K. The 153 SmH 1 ETAMoAb was prepared by a simple incubation of the MoAb ior cea1, and the 153 SmH 1 ETA complex at neutral pH and at room temperature for 24 h. The specific activity of the labelled antibody was 111 MBq/mg (3 mCi/mg). Sm-153(III) is commercially available with specific activities up to 318.2 GBq/mg. Therefore, under the conditions described above 153 SmH 1 ETA labelled MoAb could be obtained with specific activity up to 1.14 GBq/mg (30.7 mCi/mg). (author)

Phase relations in the systems M2MoO4-Cr2(MoO4)3-Zr(MoO4)2 (M=Li, Na, or Rb)

International Nuclear Information System (INIS)

Bazarov, B.G.; Chimitova, O.D.; Bazarova, Ts.T.; Arkhincheeva, S.I.; Bazarova, Zh.G.

2008-01-01

Phase equilibria in the systems M 2 MoO 4 -Cr 2 (MoO 4 ) 3 -Zr(MoO 4 ) 2 (M=Li, Na, or Rb) were investigated by X-ray powder diffraction analysis, DTA, and IR spectroscopy. The subsolidus structure of the phase diagrams of the systems under study was established. Two phases are formed in the Rb 2 MoO 4 -Cr 2 (MoO 4 ) 3 -Zr(MoO 4 ) 2 system with the molar ratios of the starting components equal to 5:1:1 (S 2 ) and 1:1:1 (S 1 ). Proceeding from isostructural character of Rb 5 FeHf(MoO 4 ) 6 and S 2 , the unit cell parameters are determined for S 2 [ru

Phase equilibria in the MgMoO4-Ln2(MoO4)3 (Ln=La,Gd) systems

International Nuclear Information System (INIS)

Fedorov, N.F.; Ipatov, V.V.; Kvyatkovskij, O.V.

1980-01-01

Phase equilibria in the MgMoO 4 -Ln 2 (MoO 4 ) 3 systems (Ln=La, Gd) have been studied by static and dynamic methods of the physico-chemical analysis, using differential thermal, visual-polythermal, crystal-optical, X-ray phase, and infrared spectroscopic methods, and their phase diagrams have been constructed. Phase equilibria in the systems studied are characterized by limited solubility of components in the liquid state, formation of solid solutions on the base of α- and β-forms of Gd 2 (MoO 4 ) 3 . Eutectics in the MgMoO 4 -Ln 2 (MoO 4 ) 3 (Ln=La, Gd) systems corresponds to the composition of 71 mode % La 2 (MoO 4 ) 3 -29 mole % MgMoO 4 , tsub(melt)--935+-5 deg C and 57 mole % Gd 2 (MoO 4 ) 3 -43 mole % MgMoO 4 , tsub(melt)=1020+-5 deg C. The region of glass formation has been established [ru

Phase equilibria in the system Li2O - MoO3 - Sc2O3

International Nuclear Information System (INIS)

Safonov, V.V.; Chaban, N.G.; Porotnikov, N.V.

1984-01-01

Using the methods of DTA and X-ray phase analysis, interaction of components in the system Li 2 O-MoO 3 -Sc 2 O 3 in concentration range, adjacent to the vertex of MoO 3 , has been studied. Projection of the Li 2 MoO 4 -MoO 3 -Sc 2 (MoO 4 ) 3 system liquidus on concentrational triangle of the compositions Li 2 O-MoO 3 -Sc 2 O 3 , which consists of the fields of primary separation of Li 2 MoO 4 , Li 2 Mo 5 O 17 , Li 2 Mo 4 O 13 , MoO 3 , Sc 2 (MoO 4 ) 3 , Li 3 Sc(MoO 4 ) 3 and LiSc(MoO 4 ) 2 , is built

Thermogravimetric and Magnetic Studies of the Oxidation and Reduction Reaction of SmCoO3 to Nanostructured Sm2O3 and Co

Science.gov (United States)

Kelly, Brian; Cichocki, Ronald; Poirier, Gerald; Unruh, Karl

The SmCoO3 to nanostructured Sm2O3 and Co oxidation and reduction reaction has been studied by thermogravimetric analysis (TGA) measurements in forming gas (FG) and inert N2 atmospheres, x-ray diffraction (XRD) and vibrating sample magnetometry (VSM). The TGA measurements showed two clearly resolvable reduction processes when heating in FG, from the initial SmCoO3 phase through an intermediate nanostructured mixture of Sm2O3 and CoO when heated to 330°C for several minutes, and then the conversion of CoO to metallic Co when heated above 500°C. These phases were confirmed by XRD and VSM. Similar measurements in N2 yielded little mass change below 900°C and coupled reduction processes at higher temperatures. Isoconversional measurements of the CoO to Co reduction reaction in FG yielded activation energies above 2eV/atom in the nanostructured system. This value is several times larger than those reported in the literature or obtained by similar measurements of bulk mixtures of Sm2O3 and CoO, suggesting the nanostructuring was the source of the large increase in activation energy.

K(MoO24O3(AsO4

Directory of Open Access Journals (Sweden)

Raja Jouini

2013-06-01

Full Text Available A new compound with a non-centrosymmetric structure, potassium tetrakis[dioxomolybdenum(IV] arsenate trioxide, K(MoO24O3(AsO4, has been synthesized by a solid-state reaction. The [(MoO24O3(AsO4]+ three-dimensional framework consists of single arsenate AsO4 tetrahedra, MoO6 octahedra, MoO5 bipyramids and bioctahedral units of edge-sharing Mo2O10 octahedra. The [Mo2O8]∞ octahedral chains running along the a-axis direction are connected through their corners to the AsO4 tetrahedra, MoO6 octahedra and MoO5 bipyramids, so as to form large tunnels propagating along the a axis in which the K+ cations are located. This structure is compared with compounds containing M2O10 (M = Mo, V, Fe dimers and with those containing M2O8 (M = V chains.

Double molybdates in Li2MoO4 - Na2MoO4 - H2O system at 25 grad C

International Nuclear Information System (INIS)

Karov, Z.G.; Mirzoev, R.S.; Makitova, D.D.; Zhilova, S.B.; Podnek, A.G.; Urusova, R.Kh.

1989-01-01

Solubility in Li 2 MoO 4 - Na 2 MoO 4 - H 2 O system at 25 deg C is first stuied. Formation of two Li 2 MoO 4 · Na 2 MoO 4 · 4H 2 O and Li 2 MoO 4 · 3Na 2 MoO 4 · 12H 2 O compounds in a system is ascertained. Density, refractive index, viscosity, surface tension, electric conductivity and pH of saturated solutions are determined. Isothermes of mole volume, equivalent and reduced electric conductivity and seeming mole volume of salts sum in solutions are calculated. All these properties adequtely confirm the character of components interaction in a system determined by solubility method. Crystallhydrates of binary molybdates are separated, indentified and studied

Interaction in the NaIn(MoO4)2 - AMoO4 (A = Mg, Mn) systems

International Nuclear Information System (INIS)

Kotova, I.Yu.; Kozhevnikova, N.M.

2001-01-01

The results of investigation into NaIn(MoO 4 ) 2 - AMoO 4 (A = Mg, Mn) quasibinary cross-sections by means of X-ray diffraction and differential thermal analysis are presented. Conducted researches revealed that compounds NaMg 3 In(MoO 4 ) and NaMn 3 In(MoO 4 ) melting incongruently at 990 Deg C and 940 Deg C accordingly were formed in the NaIn(MoO 4 ) - AMoO 4 (A = Mg, Mn) systems. The data of initiation of X-ray diffraction pattern of NaMg 3 In(MoO 4 ) 5 are presented. The temperature dependences of conductivity, dielectric permeability and tangent of dielectric losses indicative on ionic-electronic nature conductivity are determined. Activation energy of conductivity in the Mg - Mn row changes moderately - from 9.91 till 5.71 eV [ru

Hydrothermal synthesis, structure, heterogeneous catalytic activity and photoluminescent properties of a novel homoleptic Sm(III)-organic framework

Energy Technology Data Exchange (ETDEWEB)

Ay, Burak [Department of Chemistry, Arts and Science Faculty,Çukurova University, 01330 Adana (Turkey); Yildiz, Emel, E-mail: eeyildiz@cu.edu.tr [Department of Chemistry, Arts and Science Faculty,Çukurova University, 01330 Adana (Turkey); Felts, Ashley C.; Abboud, Khalil A. [Department of Chemistry, University of Florida, Gainesville, FL 32611 (United States)

2016-12-15

A novel metal-organic framework, (H{sub 2}pip){sub n}[Sm{sub 2}(pydc){sub 4}(H{sub 2}O){sub 2}]{sub n} (1) (H{sub 2}pydc=2,6-pyridinedicarboxylic acid, H{sub 2}pip=piperazine) has been synthesized under hydrothermal conditions and characterized by the elemental analysis, inductively coupled plasma (ICP) spectrometer, fourier transform infrared (FT-IR) spectra, thermogravimetric analysis (TGA), single crystal X-ray diffraction analysis and powder X-ray diffraction (PXRD). The structure of 1 was determined to be three-dimensional, linked along Sm-O-Sm chains. The asymmetric unit consisted of one singly anionic fragment consisting of Sm(III) coordinated to two H{sub 2}pydc ligands and one water, and one half of a protonated H{sub 2}pip, which sits on an inversion center. 1 exhibited luminescence emission bands at 534 nm at room temperature when excited at 440 nm. Its thermal behavior and catalytic performance were investigated and the selectivity was measured as 100% for the oxidation of thymol to thymoquinone. - Graphical abstract: A novel 3D lanthanide-organic framework has been synthesized under hydrothermal conditions. The thermal behavior and catalytic performance of 1 were investigated and its selectivity was measured as 100% for the oxidation of thymol to thymoquinone.

Phase formation in the Li2MoO4-Rb2MoO4-Ln2(MoO4)3 systems and the properties of LiRbLn2(MoO4)4

International Nuclear Information System (INIS)

Basovich, O.M.; Khajkina, E.G.; Vasil'ev, E.V.; Frolov, A.M.

1995-01-01

Phase equilibria within subsolidus range of ternary salt systems Li 2 MoO 4 -Rb 2 MoO 4 -Ln 2 (MoO 4 ) 4 (Ln - Nd, Er) are analyzed. Formation of ternary molybdate LiRbNd 2 (MoO 4 ) 4 is proved along LiNd(MoO 4 ) 2 -RbNd(MoO 4 )-2 cross-section. Phase diagram of this cross-section is plotted. Similar compounds are synthesized for Ln = La-Eu. The parameters of their monoclinic elementary cells are determined. Luminescent properties of LiRbLa 2 (MoO 4 ) 4 -Nd 3+ are studied. 17 refs., 4 figs., 2 tabs

Phase formation in the Li2MoO4–Rb2MoO4–Fe2(MoO4)3 system and crystal structure of a novel triple molybdate LiRb2Fe(MoO4)3

International Nuclear Information System (INIS)

Khal'baeva, Klara M.; Solodovnikov, Sergey F.; Khaikina, Elena G.; Kadyrova, Yuliya M.; Solodovnikova, Zoya A.; Basovich, Olga M.

2013-01-01

X-ray investigation of solid state interaction of the components in the Li 2 MoO 4 –Rb 2 MoO 4 –Fe 2 (MoO 4 ) 3 system was carried out, and a subsolidus phase diagram of the said system was constructed. The subsystem Rb 2 MoO 4 –LiRbMoO 4 –RbFe(MoO 4 ) 2 was shown to be non-quasiternary. Formation of a novel triple molybdate LiRb 2 Fe(MoO 4 ) 3 was established, conditions of solid state synthesis and crystallization of the compound were found. Its crystal structure (orthorhombic, space group Pnma, Z=4, a=24.3956(6), b=5.8306(1), c=8.4368(2) Å) represents a new structure type and includes infinite two-row ribbons ([Fe(MoO 4 ) 3 ] 3− ) ∞ parallel to the b axis and composed of FeO 6 octahedra, terminal Mo(3)O 4 tetrahedra, and bridge Mo(1)O 4 and Mo(2)O 4 tetrahedra connecting two or three FeO 6 octahedra. The ribbons are connected to form 3D framework via corner-sharing LiO 4 tetrahedra. Rubidium cations are 11- and 13-coordinated and located in cavities of this heterogeneous polyhedral framework. - Graphical abstract: Exploring the Li 2 MoO 4 –Rb 2 MoO 4 –Fe 2 (MoO 4 ) 3 system showed its partial non-quasiternarity and revealed a new compound LiRb 2 Fe(MoO 4 ) 3 which was structurally studied. - Highlights: • The Li 2 MoO 4 –Rb 2 MoO 4 –Fe 2 (MoO 4 ) 3 system study revealed a new compound LiRb 2 Fe(MoO 4 ) 3 . • Its structure of a new type includes ribbons of FeO 6 octahedra and MoO 4 tetrahedra. • The ribbons are connected into a 3D framework via corner-sharing LiO 4 tetrahedra

Interactions in the NiO-MoO3 system upon reduction

International Nuclear Information System (INIS)

Afanas'ev, P.V.; Tsurov, M.A.; Kostik, B.G.; Turakulova, A.O.

1993-01-01

Interactions in the system NiO-MoO 3 (MoO 2 ) heated in the air and in H 2 were studied by the methods of differential-thermal analysis, thermally programmed reduction, X-ray phase analysis and measurement of magnetization. In the presence of NiO the temperature of MoO 3 reduction start decreases by > 150 K. Simultaneously, in the range of temperatures 5730623 K inhibition of NiO reduction occurs, which is related to the formation of NiMo x alloy. For the samples of NiO+MoO 2 no inhibition of NiO reduction was detected, NiMo x alloy was formed after quantitative reduction of NiO

Systems Tl2MoO4-E(MoO4)2, where E=Zr or Hf, and the crystal structure of Tl8Hf(MoO4)6

International Nuclear Information System (INIS)

Bazarov, B.G.; Bazarova, Ts.T.; Fedorov, K.N.; Bazarova, Zh.G.; Chimitova, O.D.; Klevtsova, R.F.; Glinskaya, L.A.

2006-01-01

Systems Tl 2 MoO 4 -E(MoO 4 ) 2 (E=Zr, Hf) were studied by X-ray diffraction, differential thermal analysis and IR spectroscopy. Formation of Tl 8 E(MoO 4 ) 6 and Tl 2 E(MoO 4 ) 2 compounds was established. Phase T-x diagrams of the Tl 2 MoO 4 -Zr(MoO 4 ) 2 system were constructed. Monocrystals were grown, and structure of Tl 8 Hf(MoO 4 ) 6 was studied. The compound is crystallized in monoclinic syngony with elementary cell parameters a=9.9688(6), b=18.830(1), c=7.8488(5) A, β=108.538(1) Deg, Z=2, sp. gr. C2/m. The isolated group [HfMo 6 O 24 ] 8- is responsible for fundamental fragment of the structure. Three varieties of crystallographically independent Tl-polyhedra fill space evenly between fragments [HfMo 6 O 24 ] 8- forming three-dimensional form [ru

Effect of temperature for synthesizing single-walled carbon nanotubes by catalytic chemical vapor deposition over Mo-Co-MgO catalyst

International Nuclear Information System (INIS)

Niu Zhiqiang; Fang Yan

2008-01-01

The influence of temperature on synthesizing single-walled carbon nanotubes (SWCNTs) by catalytic chemical vapor deposition of methane over Mo-Co-MgO catalyst was studied by Transmission Electron Microscope (TEM) and Raman scattering. The Mo-Co-MgO bimetallic catalyst was prepared by decomposing the mixture of magnesium nitrate, ammonium molybdate, citric acid, and cobalt nitrate. The results show that Mo-Co-MgO bimetallic catalyst is effective to synthesize SWCNTs. By using Mo-Co-MgO bimetallic catalyst, generation of SWCNTs even at 940 K was demonstrated. The optimum temperature of synthesizing SWCNTs over Mo-Co-MgO bimetallic catalyst may be about 1123 K. At 1123 K, the diameters of SWCNTs are in the range of 0.75-1.65 nm. The content of SWCNTs is increased with the increase of temperature below 1123 K and the carbon yield rate is also increased with the increase of synthesis temperature. Therefore, the amount of SWCNTs increases with the increase of temperature below 1123 K. However, above 1123 K, the content of SWCNTs is decreased with the increase of temperature; therefore, it is not effective to increase the amount of SWCNTs through increasing synthesis temperature above 1123 K

Cross-Linked CoMoO4/rGO Nanosheets as Oxygen Reduction Catalyst

Directory of Open Access Journals (Sweden)

Jiaqi Fu

2017-12-01

Full Text Available Development of inexpensive and robust electrocatalysts towards oxygen reduction reaction (ORR is crucial for the cost-affordable manufacturing of metal-air batteries and fuel cells. Here we show that cross-linked CoMoO4 nanosheets and reduced graphene oxide (CoMoO4/rGO can be integrated in a hybrid material under one-pot hydrothermal conditions, yielding a composite material with promising catalytic activity for oxygen reduction reaction (ORR. Cyclic voltammetry (CV and linear sweep voltammetry (LSV were used to investigate the efficiency of the fabricated CoMoO4/rGO catalyst towards ORR in alkaline conditions. The CoMoO4/rGO composite revealed the main reduction peak and onset potential centered at 0.78 and 0.89 V (vs. RHE, respectively. This study shows that the CoMoO4/rGO composite is a highly promising catalyst for the ORR under alkaline conditions, and potential noble metal replacement cathode in fuel cells and metal-air batteries.

Luminescence enhancement in Eu3+, Sm3+ co-doped liy(MoO4)2 nano-phosphors by sol-gel process.

Science.gov (United States)

Zhou, Xianju; Wang, Guangchuan; Zhou, Tonghui; Zhou, Kaining; Li, Qingxu; Wang, Zhongqing

2014-05-01

A series of LiY(0.95-x)Eu(0.05)Sm(x)(MoO4)2 red light emitting phosphors were synthesized by sol-gel technique. The phase impurity and spectroscopic properties were characterized by X-ray Diffraction (XRD), Photo-Luminescence (PL) and Photo-Luminescence Excitation (PLE) spectra, respectively. It is found that the PLE spectra of the Eu3+, Sm3+ co-doped nanoparticles are enhanced and broadened as compared with the solely doped samples, which will make the co-doped phosphors match better with blue and/or UV GaN based LED chips. The red emission intensity of Eu3+ is largely enhanced by the energy transfer from Sm3+. The mechanism of the enhancement is clearly proven to be the increase in the quantum efficiency of 5D0 state of Eu3+ rather than the increase in the absorption of Eu3+. Meanwhile, the characteristic f-f transitions of Sm3+ are greatly reduced, resulting in little influence in the color purity of the co-doped phosphors. The present material is an amendatory promising red light emitting phosphor for white LEDs.

Structure of glasses of the TeO2-MoO3 system

International Nuclear Information System (INIS)

Dimitriev, Y.; Dimitrov, V.; Bart, J.C.J.

1981-01-01

Structural models for glasses of the TeO 2 -MoO 3 system are suggested. On the basis of X-ray and infrared spectral investigations, by comparing with known crystalline structures of TeO 2 , MoO 3 and Te 2 MoO 7 9t 2 M, it is shown that the glasses from TeO 2 to Te 2 MoO 7 possess [TeO 4 ] and [MoO 5 ] groups as basic structural units. The latter are connected to form [Mo 2 O 8 ] complexes. The glasses in the MoO 3 -rich compositional range are built up of [TeO 3 ] and [MoO 6 ] polyhedra. The glass-formation tendency is discussed in relation to the role of the free electron pair and the disruption of secondary and weak primary bonds in the crystals. (author)

Evolution of MoTeO x/SiO 2 and MoBiTeO x/SiO 2 catalysts in the partial oxidation of propane to acrolein

Science.gov (United States)

He, Yiming; Wu, Ying

2010-04-01

A thorough investigation of the catalysts Mo 1Te 1O x/SiO 2 and Mo 1Bi 0.05Te 1O x/SiO 2 in the partial oxidation of propane is presented in this paper, in order to elucidate the nature and behavior of the active surface. The catalysts' structures and redox properties were investigated by means of X-ray powder diffraction, Raman spectroscopy, in situ Raman spectroscopy, X-ray photoelectron spectroscopy, and H 2-TPR techniques. The results indicate that Te-polymolybdate is the main active phase on fresh catalysts. During reaction, the catalysts underwent a progressive reduction, resulting in the reconstruction of the active surface and the formation of a MoO 3 phase. The synergistic effect between Te-polymolybdate and MoO 3 was assumed to promote catalytic performance. The different stabilities of Mo 1Te 1O x/SiO 2 and Mo 1Bi 0.05Te 1O x/SiO 2 catalysts are also discussed.

Quatenary Na//F, Cl, CO3, MoO4 system

International Nuclear Information System (INIS)

Kochkarov, Zh.A.; Lok''yaeva, S.M.; Shurdumov, G.K.; Gasanaliev, A.M.; Trunin, A.S.

1999-01-01

Perspective in applied respect quatenary system (NaF) 2 -(NaCl)-Na 2 CO 3 -Na 2 MoO 4 being element of narrowing of more complex six-membered mutual Na//F, Cl, CO 3 , MoO 4 (WO 4 ) system is investigated by differential thermal analysis with the use of projection-thermographic method for the first time. Crystallization tree of Na//F, Cl, CO 3 , MoO 4 system is established. It is shown that this system by tetrahedrating (NaF) 2 -Na 2 CO 3 -Na 3 ClMoO 4 section is triangulated on two stable system: (NaF) 2 -Na 3 ClMoO 4 -Na 2 CO 3 -(NaCl) 2 and (NaF) 2 -Na 3 ClMoO 4 -Na 2 CO 3 -Na 2 MoO 4 . Phase single units are determined too. Coordinates of desired quatenary nonvariant points are calculated on analytical models of surfaces by mutual crystallization of two phases and are refined by differential thermal analysis [ru

Phase formation in the Rb2MoO4-Li2MoO4-Hf(MoO4)2 system and the crystal structure of Rb5(Li1/3Hf5/3)(MoO4)6

International Nuclear Information System (INIS)

Solodovnikov, S.F.; Zolotova, E.S.; Balsanova, L.V.; Bazarov, B.G.; Bazarova, Zh.G.

2003-01-01

Phase formation in the Rb 2 MoO 4 -Li 2 MoO 4 -Hf(MoO 4 ) 2 system is studied in subsolidus region in air by the method of crossing sections. Three ternary molybdates are detected in the system. Compositions of two of them are corroborated by selection of isostructural analogues [ru

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...

On the coexistence of copper-molybdenum bronzes: CuxMoO3 (0.2 yMoO3-z (0.1 2-O quasi-ternary system

International Nuclear Information System (INIS)

Warner, T.E.; Skou, E.M.

2010-01-01

Two copper-molybdenum bronzes: Cu y MoO 3-z (0.1 x MoO 3 (0.2 3 at 600 o C under argon in Pt crucibles. Powder XRD showed that the material with global composition '0.1Cu.MoO 3 ' comprises ∼Cu 0.15 MoO 3 and MoO 3 ; whilst '0.2Cu.MoO 3 ' comprises ∼Cu 0.15 MoO 3 and ∼Cu 0.23 MoO 3 . DTA performed on '0.2Cu.MoO 3 ' reveals a reversible solid state phase transition ∼520 o C under argon. Reacting equimolar amounts of Cu 2 O and MoO 2 at 600 o C in a Cu crucible under argon yields: Cu 6 Mo 5 O 18 , Cu and MoO 2 . A tentative subsolidus Cu-MoO 2 -O isothermal (∼25 o C) phase diagram under argon is drawn from these data. Oxidation states of Cu and Mo within this system are discussed.

Narrow band gap and visible light-driven photocatalysis of V-doped Bi{sub 6}Mo{sub 2}O{sub 15} nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Xu, Jian; Qin, Chuanxiang; Huang, Yanlin [State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Wang, Yaorong, E-mail: yrwang@suda.edu.cn [State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Qin, Lin [Department of Physics and Interdisciplinary Program of Biomedical, Mechanical & Electrical Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of); Seo, Hyo Jin, E-mail: hjseo@pknu.ac.kr [Department of Physics and Interdisciplinary Program of Biomedical, Mechanical & Electrical Engineering, Pukyong National University, Busan 608-737 (Korea, Republic of)

2017-02-28

Highlights: • V{sup 5+}-doped Bi{sub 6}Mo{sub 2}O{sub 15} was synthesized by the electrospinning preparation. • The band gap energy of Bi{sub 6}Mo{sub 2}O{sub 15} was greatly reduced by V-doping in the lattices. • V-doped Bi{sub 6}Mo{sub 2}O{sub 15} shows high activity in RhB degradation under visible light. • Crystal structure of Bi{sub 6}Mo{sub 2}O{sub 15} is favorable for high photocatalytic capacity. - Abstract: Pure and V{sup 5+}-doped Bi{sub 6}Mo{sub 2}O{sub 15} (3Bi{sub 2}O{sub 3}·2MoO{sub 3}) photocatalysts were synthesized through electrospinning, followed by low-temperature heat treatment. The samples developed into nanoparticles with an average size of approximately 50 nm. The crystalline phases were verified via X-ray powder diffraction measurements (XRD). The surface properties of the photocatalysts were studied by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) analyses. The UV–vis spectra showed that V doping in Bi{sub 6}Mo{sub 2}O{sub 15} shifted the optical absorption from the UV region to the visible-light wavelength region. The energy of the band gap of Bi{sub 6}Mo{sub 2}O{sub 15} was reduced by V doping in the lattices. The photocatalytic activities of the pure and V-doped Bi{sub 6}Mo{sub 2}O{sub 15} were tested through photodegradation of rhodamine B (RhB) dye solutions under visible light irradiation. Results showed that 20 mol% V-doped Bi{sub 6}Mo{sub 2}O{sub 15} achieved efficient photocatalytic ability. RhB could be degraded by V-doped Bi{sub 6}Mo{sub 2}O{sub 15} in 2 h. The photocatalytic activities and mechanisms were discussed according to the characteristics of the crystal structure and the results of EIS and XPS measurements.

Crystal structure of Sm(NO3)3x6H2O

International Nuclear Information System (INIS)

Espenbetov, A.A.; Gerr, R.G.; Struchkov, Yu.T.; Sal'nikova, N.A.; Akimov, V.M.; Odinets, Z.K.

1985-01-01

X-ray diffraction study of a salt, prepared when mixing concentrated nitric acid solutions of NaNO 3 and Sm(NO 3 ) 3 , has been carried out. It is established, that the salt is a concretion of two crystals: NaNO 3 and Sm(NO 3 ) 3 x6H 2 O (1). X-ray diffraction study of 1 is carried out (lambda Mo, diffractometer, 1511 reflections, the method of heavy atom, the least square method in anisotropic approximation up to R=0.0348). The crystals of 1 are triclinic: a=6.755, b=9.168, c=11.684 A, α=69.93, β=88.86, γ=69.28, Z=2, Fedorov group P anti 1. Symmetery of 10-vertex coordination polyhedron (CP) of Sm atom is close to Csub(s). Sm atom coordination can be described as 4;5:1. Four H 2 O molecules are included into CP, at the expense of two remaining H 2 O molecules CP are bound with each other

Phase equilibria in the Tl2MoO4–R2(MoO43–Zr(MoO42 (R = Al, Cr systems: synthesis, structure and properties of new triple molybdates Tl5RZr(MoO46 and TlRZr0.5(MoO43

Directory of Open Access Journals (Sweden)

V. G. Grossman

2017-12-01

Full Text Available The Tl2MoO4–R2(MoO43–Zr(MoO42 (R = Al, Cr systems were studied in the subsolidus region using X-ray powder diffraction and differential scanning calorimetric (DSC analysis. Quasi-binary joins were revealed, and triangulation was carried out. New ternary molybdates: Tl5RZr(MoO46 (5:1:2 and TlRZr0.5(MoO43 (1:1:1 (R = Al, Cr were prepared. The unit cell parameters for the new compounds were calculated.

Improving the stability of subnano-MoO3/meso-SiO2 catalyst through amino-functionalization

Science.gov (United States)

Wang, Jiasheng; Wu, Wenpei; Yang, Qianfan; Wang, Wan-Hui; Bao, Ming

Subnano-MoO3 clusters (below 1nm) have excellent catalytic activity on oxidative desulfurization (ODS). However, the stability is not very satisfactory due to the leaching of MoO3 during the reaction. To enhance the stability, here we developed a method by grafting NH2 to silica. NH2 could form coordination bond with MoO3, as proved by solid state 1H NMR, which can prevent MoO3 from leaching and thus significantly enhance the stability.

Quaternary reciprocal system Na,K//Cl,Co3,MoO4

International Nuclear Information System (INIS)

Kochkarov, Zh.A.; Gasanaliev, A.M.

2004-01-01

Quaternary reciprocal system Na,K//Cl,Co 3 ,MoO 4 has been investigated for the first time by differential thermal analysis using the methods of projective and differential geometry. A stable (KCl) 2 -Na 2 CO 3 -K 2 CO 3 -K 2 MoO 4 tetrahedron and (NaCl) 2 -(KCl) 2 -Na 2 CO 3 -K 2 MoO 4 -Na 2 MoO 4 pentatope have been revealed in the system. It has been found that four quadruple invariant points are realized in the Na,K//Cl,Co 3 ,MoO 4 system, including one eutectic and three peritectic points [ru

Structural and electrochemical properties of single crystalline MoV 2O8 nanowires for energy storage devices

KAUST Repository

Shahid, Muhammad; Liu, Jingling; Ali, Zahid; Shakir, Imran; Warsi, Muhammad Farooq

2013-01-01

We report the synthesis of MoV2O8 nanowires of high quality using spin coating followed by the thermal annealing process. Transmission electron microscopy (TEM) reveals the average diameter of synthesized nanowire about 100 nm, and average length ranges from 1 to 5 μm. The TEM analysis further confirms the <001> growth direction of MoV 2O8 nanowires. The electrochemical properties of synthesized nanowires using cyclic voltammetry show the specific capacitance 56 Fg-1 at the scan rate of 5 mV s-1 that remains 24 Fg -1 at 100 mV s-1. The electrochemical measurements suggest that the MoV2O8 nanowires can be used as a material for the future electrochemical capacitors (energy storage devices). © 2012 Published by Elsevier Inc. All rights reserved.

Structural and electrochemical properties of single crystalline MoV 2O8 nanowires for energy storage devices

KAUST Repository

Shahid, Muhammad

2013-05-01

We report the synthesis of MoV2O8 nanowires of high quality using spin coating followed by the thermal annealing process. Transmission electron microscopy (TEM) reveals the average diameter of synthesized nanowire about 100 nm, and average length ranges from 1 to 5 μm. The TEM analysis further confirms the <001> growth direction of MoV 2O8 nanowires. The electrochemical properties of synthesized nanowires using cyclic voltammetry show the specific capacitance 56 Fg-1 at the scan rate of 5 mV s-1 that remains 24 Fg -1 at 100 mV s-1. The electrochemical measurements suggest that the MoV2O8 nanowires can be used as a material for the future electrochemical capacitors (energy storage devices). © 2012 Published by Elsevier Inc. All rights reserved.

Study of the Mo(VI) catalytic response in the oxidation of iodide by hydrogen peroxide using a monosegmented continuous-flow system

International Nuclear Information System (INIS)

Andrade, J.C. de; Eiras, S.P.; Bruns, R.E.

1991-01-01

Fractional factorial, modified simplex and response surface studies of the Mo(VI)-catalysed and non-catalysed oxidation of iodide by hydrogen peroxide in acidic medium were executed using a monosegmented continuous-flow system (MCFS). As this reaction is commonly used for the spectrophotometric catalytic determination of Mo(VI), the behaviour of the analytically useful response, ΔA, the difference of the average absorbance values of the Mo(VI)-catalysed and non-catalysed reactions, was studied over a large range of experimental conditions. The effects of simultaneous changes in the sample flow-rate, the H 2 SO 4 , KI and H 2 O 2 concentrations and the reaction time on the signals were measured. The optimum concentrations found using MCFS are 0.0665, 0.1528 and 0.0041 M for H 2 SO 4 , KI and H 2 O 2 , respectively. Rigorous control of the acid concentration is essential to maintain the sensitivity of the analytical signal for operating conditions close to the optimum values recommended here. On the other hand, the ΔA values are much less sensitive to variations in the H 2 O 2 concentration. Increasing KI concentrations can improve the sensitivity but can also cause baseline instability. The response surface is convenient for visualizing the overall behaviour of the system for the experimental control values investigated. (author). 24 refs.; 3 figs.; 1 tab

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

Study of phase equilibria in LiIn(MoO4)2 - MeIn(MoO4)2 (Me - K, Rb) systems

International Nuclear Information System (INIS)

Smirnyagina, N.N.; Kozhevnikova, N.M.; Alekseev, F.P.; Mokhosoev, M.V.

1983-01-01

To determine the possibilities of formation of ternary molybdates, containing two different alkali cations and a cation of trivalent element, the qUasibinary LiIn(MoO 4 ) 2 -MeIn(MoO 4 ) 2 cross-sections of quaternary Li 2 O-Me 2 O-In 2 O 3 -MoO 3 , (Me-K, Rb) systems have been studied. Methods of X-ray phase-, differential thermal- and crystal optical analyses were used. The studied systems are eutectics with segregation; ternary compounds are not formed in theM

Thermal expansion studies on Th(MoO4)2, Na2Th(MoO4)3 and Na4Th(MoO4)4

International Nuclear Information System (INIS)

Keskar, Meera; Krishnan, K.; Dahale, N.D.

2008-01-01

Thermal expansion behavior of Th(MoO 4 ) 2 , Na 2 Th(MoO 4 ) 3 and Na 4 Th(MoO 4 ) 4 was studied under vacuum in the temperature range of 298-1123 K by high temperature X-ray diffractometer. Th(MoO 4 ) 2 was synthesized by reacting ThO 2 with 2 mol of MoO 3 , at 1073 K in air and Na 2 Th(MoO 4 ) 3 and Na 4 Th(MoO 4 ) 4 were prepared by reacting Th(MoO 4 ) 2 with 1 and 2 mol of Na 2 MoO 4 , respectively at 873 K in air. The XRD data of Th(MoO 4 ) 2 was indexed on orthorhombic system where as XRD data of Na 2 Th(MoO 4 ) 3 and Na 4 Th(MoO 4 ) 4 were indexed on tetragonal system. The lattice parameters and cell volume of all the three compounds, fit into polynomial expression with respect to temperature, showed positive thermal expansion (PTE) up to 1123 K. The average value of thermal expansion coefficients for Th(MoO 4 ) 2 , Na 2 Th(MoO 4 ) 3 and Na 4 Th(MoO 4 ) 4 were determined from the high temperature data

Bulk magnetic characterization of RCaCrO4 (Rrl02=Y, Pr, Sm ) oxides

International Nuclear Information System (INIS)

Martinez, J.L.; Fernandez-Diaz, M.T.; Chen, Q.; Prieto, C.; Andres, A. de; Saez-Puche, R.; Romero, J.

1995-01-01

The system RCaCrO 4 (R=Y, Sm, Pr) presents an orthorhombic structure (space group Bmab) at room temperature (RT), similar to that observed in La 2 MO 4 (M=Cu, Ni, Co). The magnetic susceptibility for RCaCrO 4 shows a weak temperature dependence down to 250 K, probably due to the antiferromagnetic ordering of the Cr sublattice above RT. Below RT there is a strong upturn anomaly at 210, 190 and 130 K for Pr, Sm and Y, respectively. This anomaly is associated with the appearance of a weak ferromagnetic component, and could be related to a low temperature structural phase transition, similar to that observed in the related compounds R 2 NiO 4 or La 1.88 Ba 0.12 CuO 4 . In the case of YCaCrO 4 this ferromagnetic component produces a hysteresis curve at 4.5 K with a coercive field of 0.7 T. For PrCaCrO 4 the coercive field is very small ( 4 shows a more complicated behavior with a low temperature magnetic transition (T N2 ∼40 K), which could be associated with either the antiferromagnetic ordering of the Sm sublattice or a spin reorientation in the Cr sublattice. ((orig.))

NOx Selective Catalytic Reduction (SCR) on Self-Supported V-W-doped TiO2 Nanofibers

DEFF Research Database (Denmark)

Marani, Debora; Silva, Rafael Hubert; Dankeaw, Apiwat

2017-01-01

Electrospun V–W–TiO2 catalysts, resulting in a solid solution of V and W in the anatase phase, are prepared as nonwoven nanofibers for NOx selective catalytic reduction (SCR). Preliminary catalytic characterization indicates their superior NOx conversion efficiency to the-state-of-the-art materia...

Phase formation in K2O(K2CO3)-CdO-MoO3 system

International Nuclear Information System (INIS)

Tsirenova, G.D.; Tsybikova, B.A.; Bazarova, Zh.G.; Solodovnikov, S.F.; Zolotova, E.S.

2000-01-01

Phase formation in K 2 O(K 2 CO 3 )-CdO-MoO 3 system are studied by the methods of x-ray diffraction, thermal and crystal optical analyses. Three potassium-cadmium molybdates are detected: K 4 Cd(MoO 4 ) 3 with a new structure, alluodite-like K 4-2x Cd 1+x (MoO 4 ) 3 (0.26≤x≤0.38 at 470 Deg C) and K 4 CdMo 4 O 15 of K 4 MnMo 4 O 15 type. First of them decomposes in solid phase at 580 Deg C, and others melt incongruently at 720 and 515 Deg C correspondingly. It is established that K 4-2x Cd 1+x (MoO 4 ) 3 compound undergoes phase transition of the second type in the temperature interval of 500-550 Deg C. Phase diagram of quasibinary cross section K 2 MoO 4 -CdMoO 4 is plotted [ru

Study on Mo(V) species, location and adsorbates interactions in MoH-SAPO-34 by employing ESR and electron spin-echo modulation spectroscopies

International Nuclear Information System (INIS)

Back, Gern Ho; Jang, Chang Ki; Ru, Chang Kuk; Cho, Young Hwan; So, Hyun Soo; Larry, Keven

2002-01-01

A solid-state reaction of MoO 3 with as-synthesized H-SAPO-34 generated paramagnetic Mo(V) species. The dehydration resulted in weak Mo(V) species, and subsequent activation resulted in the formation of Mo(V) species such as Mo(V) 5c and Mo(V) 6c that are characterized by ESR. The data of ESR and ESEM show the oxomolybdenum species, to be (MoO 2 ) + or (MoO) 3+ . The (MoO 2 ) + species seems to be more probable. Since H-SAPO-34 has a low framework negative charge, (MoO) 3+ with a high positive charge can not be easily stabilized. A solution reaction between the solution of silico-molybdic acid and calcined H-SAPO-34 resulted in only MoO + 2 species. A rhombic ESR signal is observed on adsorption of D 2 O, CD 3 OH, CH 3 CH 2 OD and ND 3 . The Location and coordination structure of Mo(V) species has been determined by three-pulse electron spin-echo modulation data and their simulations. After the adsorption of methanol, ethylene, ammonia, and water for MoH-SAPO-34, three molecules, one and one molecule, respectively, are directly coordinated to (MoO 2 ) +

Epitaxial (100)-oriented Mo/V superlattice grown on MgO(100) by dcMS and HiPIMS

International Nuclear Information System (INIS)

Shayestehaminzadeh, S.; Magnusson, R.L.; Gislason, H.P.; Olafsson, S.

2013-01-01

Epitaxial (100)-oriented Mo/V superlattices have been grown by High Power Impulse Magnetron Sputtering (HiPIMS) and dc Magnetron Sputtering (dcMS) on single-crystalline MgO(100) substrates at growth temperatures ranging from 30 °C to 600 °C. Superlattice bilayer period of Mo/V around 12/12 monolayers and 15 repeat periods was studied. This study aims to investigate the effect of the HiPIMS process on reducing the growth temperature of Mo/V superlattices using the high energy ionized Mo, V species in the HiPIMS plasma. In one case, the Mo layer was only grown with the HiPIMS process and V layer grown using the dcMS process while in another both layers were grown with the HiPIMS process. The as-deposited films were characterized by X-ray reflection and diffraction techniques. The dcMS process was found to give superior superlattice growth at high growth temperatures while a mixed Mo HiPIMS and V dcMS process gives better result at lower growth temperatures (300 °C). Room temperature growth reveals that neither the mixed Mo HiPIMS and V dcMS process nor the pure HiPIMS for both materials can produce better result compared to the pure dcMS process, which gives a relatively better result. - Highlights: • Epitaxial (100)-oriented Mo/V superlattices have been grown by HiPIMS and dcMS on MgO(100) for various temperatures. • The study was aimed to investigate the effect of ionized HiPIMS process onlowering the growth temperature. • The dcMS process was found to give superior superlattice growth at high growth temperature. • The mixed Mo HiPIMS and V dcMS process gives best result at lower growth temperatures

Phase diagrams for the M2MoO4–Ln2(MoO43–Hf(MoO42 systems, where M = Li–Cs, Tl and Ln = La–Lu

Directory of Open Access Journals (Sweden)

Zh. G. Bazarova

2017-12-01

Full Text Available In this paper, the results of systematic studies of complex molybdate systems M2MoO4–Ln2(MoO43–Hf(MoO42 (M = Li–Cs, Tl; Ln = La–Lu are presented. Subsolidus phase diagrams of ternary systems were constructed and new triple molybdates were obtained. The optimum synthesis conditions for poly- and monocrystalline form were determined. According to single-crystal data, the structure of one of the representatives of triple molybdates was determined.

Nanocrystalline Mn-Mo-Ce Oxide Anode Doped Rare Earth Ce and Its Selective Electro-catalytic Performance

Directory of Open Access Journals (Sweden)

SHI Yan-hua

2017-09-01

Full Text Available The anode oxide of nanocrystalline Mn-Mo-Ce was prepared by anode electro-deposition technology, and its nanostructure and selective electro-catalytic performance were investigated using the SEM, EDS, XRD, HRTEM, electrochemical technology and oxygen evolution efficiency testing. Furthermore, the selective electro-catalytic mechanism of oxygen evolution and chlorine depression was discussed. The results show that the mesh-like nanostructure Mn-Mo-Ce oxide anode with little cerium doped is obtained, and the oxygen evolution efficiency for the anode in the seawater is 99.51%, which means a high efficiency for the selective electro-catalytic for the oxygen evolution. Due to the structural characteristics of γ-MnO2, the OH- ion is preferentially absorbed, while Cl- absorption is depressed. OH- accomplishes the oxygen evolution process during the valence transition electrocatalysis of Mn4+/Mn3+, completing the selective electro-catalysis process. Ce doping greatly increases the reaction activity, and promotes the absorption and discharge; the rising interplanar spacing between active (100 crystalline plane promotes OH- motion and the escape of newborn O2, so that the selective electro-catalytic property with high efficient oxygen evolution and chlorine depression is achieved from the nano morphology effect.

Catalytic Enhancement of Carbon Black and Coal-Fueled Hybrid Direct Carbon Fuel Cells

DEFF Research Database (Denmark)

Deleebeeck, Lisa; Ippolito, Davide; Kammer Hansen, Kent

2015-01-01

, Ce1-xREExO2-δ (REE = Pr, Sm)) and metal oxides (LiMn2O4, Ag2O). Materials showing the highest activity in carbon black (Mn2O3, CeO2, Ce0.6Pr0.4O2-δ, Ag2O) were subsequently tested for catalytic activity toward bituminous coal, as revealed by both I-V-P curves and electrochemical impedance...... spectroscopy (EIS). Catalytic activity was evaluated as a function of various physical characteristics of doped ceria and manganese-based materials....

Catalytic properties of pure and K+-doped Cu O/Mg O system towards 2-propanol conversion

International Nuclear Information System (INIS)

El-Molla, S. A.; Amin, N. H.; Hammed, M. N.; Sultan, S. N.; El-Shobaky, G. A.

2013-01-01

Cu O/Mg O system having different compositions was prepared by impregnation method followed by calcination at 400-900 C. The effect of Cu O content, calcination temperature and doping with small amounts of K + species (1-3 mol %) on physicochemical, surface and catalytic properties of the system were investigated using X-ray diffraction, adsorption of N 2 at - 196 C, and conversion of isopropyl alcohol at 150-400 C using a flow technique. The results revealed that the solids having the formulae 0.2 and 0.3 Cu O/Mg O calcined at 400 C consisted of nano sized Mg O and Cu O as major phases together with Cu 2 O as minor phase. The Bet-surface areas of different absorbents are decreased by increasing Cu O content, calcination temperature and K + -doping. Mg O-support material showed very small catalytic activity in 2-propanol conversion. The investigated system behaved as selective catalyst for dehydrogenation of 2-propanol with selectivity >80%. The catalytic activity increased by increasing Cu O content and decreased by increasing the calcination temperature within 400-900 C. K + -doping increased the catalytic activity and catalytic durability. (Author)

Controllable synthesis of carbon nanotubes by changing the Mo content in bimetallic Fe-Mo/MgO catalyst

International Nuclear Information System (INIS)

Xu Xiangju; Huang Shaoming; Yang Zhi; Zou Chao; Jiang Junfan; Shang Zhijie

2011-01-01

Research highlights: → Increasing the Mo content in the Fe-Mo/MgO catalysts resulted in an increase in wall number, diameter and growth yield of carbon nanotubes. → The Fe interacts with MgO to form complex (MgO) x (FeO) 1-x (0 4 and relative large metal Mo particles can be generated after reduction. → The avalanche-like reduction of MgMoO 4 makes the catalyst particles to be small thus enhances the utilize efficiency of Fe nanoparticles. - Abstract: A series of Fe-Mo/MgO catalysts with different Mo content were prepared by combustion method and used as catalysts for carbon nanotube (CNT) growth. Transmission electron microscopy studies of the nanotubes show that the number of the CNT walls and the CNT diameters increase with the increasing of Mo content in the bimetallic catalyst. The growth yield determined by thermogravimetric analysis also follows the trend: the higher the Mo content, the higher the yield of the CNTs. However, the increase of Mo content leads to the lower degree of graphitization of CNTs. A comparative study on the morphology and catalytic functions of Fe/MgO, Mo/MgO and Fe-Mo/MgO catalysts was carried out by scanning electron microscopy and X-ray diffraction. It is found that the Fe interacts with MgO to form complexes and is then dispersed into the MgO support uniformly, resulting in very small Fe nanoparticles after reduction. The Mo interacts with MgO to form stoichiometry compound MgMoO 4 and relative large metal Mo particles can be generated after reduction. High yield CNTs with small diameter can be generated from Fe-Mo/MgO because the avalanche-like reduction of MgMoO 4 makes the catalyst particles to be small thus enhances the utilize efficiency of Fe nanoparticles.

Na2MoO2As2O7

Directory of Open Access Journals (Sweden)

Raja Jouini

2012-12-01

Full Text Available Disodium molybdenum dioxide diarsenate, Na2MoO2As2O7, has been synthesized by a solid-state reaction. The structure is built up from MoAs2O12 linear units sharing corners to form a three-dimensional framework containing tunnels running along the a-axis direction in which the Na+ cations are located. In this framework, the AsV atoms are tetrahedrally coordinated and form an As2O7 group. The MoVI atom is displaced from the center of an octahedron of O atoms. Two Na+ cations are disordered about inversion centres. Structural relationships between different compounds: A2MoO2As2O7 (A = K, Rb, AMOP2O7 (A = Na, K, Rb; M = Mo, Nb and MoP2O7 are discussed.

Physicochemical study of properties of complex oxides of the system Li2O-MoO3-SnO2

International Nuclear Information System (INIS)

Safonov, V.V.; Chaban, N.G.; Kuz'mina, N.P.; Vashman, A.A.; Petrov, K.I.

1990-01-01

By the method of differential thermal analysis using X-ray phase analysis in the Li 2 O-MoO 3 -SnO 2 system (Li 2 Sn(MoO 4 ) 3 -Sn(MoO 4 ) 2 cross section) formation of a new complex of the composition Li 2 Sn 3 (MoO 4 ) 7 incongruently melting at 480 deg C is ascertained. IR, Raman and NMR spectra of Li 4 SnMo 2 O 10 , Li 2 Sn(MoO 4 ) 3 and Li 2 Sn 3 (MoO 4 ) 7 complex oxides are presented. According to 7 Li NMR spectra of Li 4 SnMo 2 O 10 , Li 2 Sn(MoO 4 ) 3 and Li 2 Sn 3 (MoO 4 ) 7 complex are presented. According to 7 Li NMR spectra the value of the lithium diffusion increases in the series Li 4 SnMo 2 O 10 →Li 2 Sn(MoO 4 ) 3 →Li 2 Sn 3 (MoO 4 ) 7

Room temperature synthesis and photocatalytic property of AgO/Ag2Mo2O7 heterojunction nanowires

International Nuclear Information System (INIS)

Hashim, Muhammad; Hu, Chenguo; Wang, Xue; Wan, Buyong; Xu, Jing

2012-01-01

Graphical abstract: The AgO nanoparticles are attached on the surface of the Ag 2 Mo 2 O 7 nanowires to form a heterojunction structure. The AgO nanoparticles start embedding into the nanowires with increasing reaction temperature or time. Highlights: ► AgO/Ag 2 Mo 2 O 7 heterojunction NWs were synthesized at room temperature for the first time. ► AgO particles embed into the Ag 2 Mo 2 O 7 NWs with increase in reaction time and temperature. ► The heterojunction NWs display much better photocatalytic activity than the none-heterojunction NWs. ► The catalytic mechanism was proposed. -- Abstract: AgO/Ag 2 Mo 2 O 7 heterojunction nanowires were synthesized at temperatures of 25 °C, 50 °C, 80 °C, and 110 °C, under magnetic stirring in solution reaction. The catalytic activity of AgO/Ag 2 Mo 2 O 7 nanowires was evaluated by the degradation of Rhodmine B dye under the irradiation of the simulated sunlight. The synthesized samples were characterized by X-ray diffractometer, energy dispersive spectrometry, X-ray photoelectron spectrometer, scanning electron microscopy, and transmission electron microscopy. The results show that the AgO nanoparticles are attached on the surface of the Ag 2 Mo 2 O 7 nanowires to form a heterojunction structure. The length of the nanowires is up to 10 μm and the size of the AgO nanoparticles is 10–20 nm. The length of nanowires increases with increasing reaction time and temperature while the AgO particles are gradually embedded into the nanowires. The photocatalytic activity is greatly improved for the AgO/Ag 2 Mo 2 O 7 heterojunction nanowires compared with that of the pure Ag 2 Mo 2 O 7 nanowires, indicating a remarkable role of AgO particles on the Ag 2 Mo 2 O 7 nanowires in the photodegradation.

Zn-Mo/HZSM-5 Catalyst for Gasoil Range Hydrocarbon Production by Catalytic Hydrocracking of Ceiba pentandra oil

Directory of Open Access Journals (Sweden)

Yustia Wulandari Mirzayanti

2018-01-01

Full Text Available Biofuel from vegetable oil becomes one of the most suitable and logical alternatives to replace fossil fuel. The research focused on various metal ratio Zinc/Molybdenum/HZSM-5 (Zn-Mo/HZSM-5 catalyst to produce liquid hydrocarbon via catalytic hydrocracking of Ceiba penandra oil. The catalytic hydrocracking process has been applied in this study to crack Ceiba pentandra oil into a gasoil range hydrocarbon using Zn-Mo/HZSM-5 as a catalyst. The effect of various reaction temperature on the catalytic hydrocracking of Ceiba pentandra oil were studied. The Zn-Mo/HZSM-5 catalyst with metal ratio was prepared by incipient wetness impregnation method. This process used slurry pressure batch reactor with a mechanical stirrer. A series of experiments were carried out in the temperature range from 300-400 oC for 2 h at pressure between 10-15 bar. The conversion and selectivity were estimated. The liquid hydrocarbon product were identified to gasoline, kerosene, and gas oil. The results show that the use of Zn-Mo/HZSM-5 can produce gas oil as the most component in the product. Overall, the highest conversion and selectivity of gas oil range hydrocarbon was obtained when the ZnMo/HZSM-5 metal ratio was Zn(2.86 wt.%-Mo(5.32 wt.%/HZSM-5 and the name is Zn-Mo/HZSM-5_102. The highest conversion was obtained at 63.31 % and n-paraffin (gas oil range selectivity was obtained at 90.75 % at a temperature of 400 oC. Ceiba pentandra oil can be recommended as the source of inedible vegetable oil to produce gasoil as an environmentally friendly transportation fuel. Copyright © 2018 BCREC Group. All rights reserved Received: 8th September 2017; Revised: 9th September 2017; Accepted: 17th September 2017; Available online: 22nd January 2018; Published regularly: 2nd April 2018 How to Cite: Mirzayanti, Y.W., Kurniawansyah, F., Prajitno, D.H., Roesyadi, A. (2018. Zn-Mo/HZSM-5 Catalyst for Gasoil Range Hydrocarbon Production by Catalytic Hydrocracking of Ceiba pentandra

Mo-doped V2O5 hierarchical nanorod/nanoparticle core/shell porous microspheres with improved performance for cathode of lithium-ion battery

Science.gov (United States)

Yu, Haolin; Zeng, Jianyun; Hao, Wen; Zhou, Peng; Wen, Xiaogang

2018-05-01

Mo-doped V2O5 hierarchical nanorod/nanoparticle core/shell porous microspheres (MVHPMs) were prepared via a simple hydrothermal approach using ammonium metavanadate and ammonium molybdate as precursors followed by a thermal annealing process. The samples were characterized by XRD, SEM, TEM, EDS, and XPS carefully; it confirmed that porous microspheres with uniform Mo doping in the V2O5 matrix were obtained, and it contains an inner core self-assembled with 1D nanorods and outer shell consisting of nanoparticles. A plausible growth mechanism of Mo-doped V2O5 (Mo-V2O5) porous microspheres is suggested. The unique microstructure made the Mo-V2O5 hierarchical microspheres a good cathode material for Li-ion battery. The results indicate the synthesized Mo-V2O5 hierarchical microspheres exhibit well-improved electrochemical performance compared to the undoped samples. It delivers a high initial reversible capacity of 282 mAh g-1 at 0.2 C, 208 mAh g-1 at 2 C, and 111 mAh g-1 at 10 C, and it also exhibits good cycling stabilities; a capacity of 144 mAh g-1 is obtained after 200 cycles at 6 C with a capacity retention of > 82%, which is much high than that of pure V2O5 (95 mAh g-1 with a capacity retention of 72%). [Figure not available: see fulltext.

LiVO/sub 3/-Li/sub 2/Mo(W)O/sub 4/ and NaVO/sub 3/-Na/sub 2/Cr(Mo)O/sub 4/ systems

Energy Technology Data Exchange (ETDEWEB)

Belyaev, I N; Lupeiko, T G; Vyalikova, V I [Rostovskij-na-Donu Gosudarstvennyj Univ. (USSR)

1975-09-01

The systems LiVO/sub 3/-Li/sub 2/MoO/sub 4/, LiVO/sub 3/-Li/sub 2/WO/sub 4/, NaNO/sub 3/-Na/sub 2/CrO/sub 4/, NaNO/sub 3/-Na/sub 2/MoO/sub 4/ were studied with thermographic and partially visual polythermal methods of physical and chemical analyses. Except NaVO/sub 3/-Na/sub 2/MoO/sub 4/ all investigated systems are eutectic ones with limited solid solutions on the basis of some component; the eutectics melt at 542, 544, 550/sup 0/C and contain 25, 20 and 26% of Li/sub 2/MoO/sub 4/, Li/sub 2/WO/sub 4/ and Na/sub 2/CrO/sub 4/ respectively. The system NaNO/sub 3/-Na/sub 2/MoO/sub 4/ contains compound 18 NaVO/sub 3/.11Na/sub 2/MoO/sub 4/ congruently melting at 570/sup 0/C. Two eutectics of the system have melting points at 542 and 548/sup 0/C and contain 47 and 67% of Na/sub 2/MoO/sub 4/.

Formaldehyde formation in coupled oxidation of methane and methanol over V2O5 and MoO3 silica supported catalysts

International Nuclear Information System (INIS)

Lojewska, J.; Makowski, W.; Fajardo Farre, A.; Dziembaj, R.

2003-01-01

The effect of methanol on partial oxidation of methane has been studied on standard molybdena and vanadia catalysts supported on silica. Prior to catalytic tests the catalysts were characterized by BET, SEM/EDAX and TPR/O methods. Three types of catalytic tests were performed giving temperature and contact time dependence on the catalyst activity and selectivity: partial oxidations of methane, methanol and methane/methanol mixtures. The methanol showed an activating impact on the partial oxidation of methane over all used catalysts samples, but the strongest one over Mo 3 /SiO 2 . In the absence of CH 3 OH the only catalyst, which exhibited HCHO selectivity, was low loaded vanadia catalyst. It has been put forward that methanol may enhance formation of oxygen active species, prerequisites for activating methane molecules, through reducing vanadia cations and causing breakage of vanadium oxygen bonds. (author)

Phase equilibrium in Rb2MoO4-AMoO4-Zr(MOO4)2 systems (A - bivalent elements)

International Nuclear Information System (INIS)

Ivanova, M.N.; Tsyrenova, G.D.; Bazarova, Zh.G.

1993-01-01

The Rb 2 MoO 4 -AMoO 4 -Zr(MoO 4 ) 2 systems, where A - bivalent elements, were investigated by solid phase reactions, x-ray and differntial thermal analysis methods. Formation of new ternary molybdates was determined. Phase relationships in the Rb 2 MoO 4 -MnMoO 4 -Zr(MoO 4 ) 2 system in subsolidus range (550 deg C) were studied using x-ray analysis data

The Effect of Acidic and Redox Properties of V2O5/CeO2-ZrO2 Catalysts in Selective Catalytic Reduction of NO by NH3

DEFF Research Database (Denmark)

Putluru, Siva Sankar Reddy; Riisager, Anders; Fehrmann, Rasmus

2009-01-01

V2O5 supported ZrO2 and CeO2–ZrO2 catalysts were prepared and characterized by N2 physisorption, XRPD, TPR, and NH3-TPD methods. The influence of calcination temperature from 400 to 600 °C on crystallinity, acidic and redox properties were studied and compared with the catalytic activity...... in the selective catalytic reduction (SCR) of NO with ammonia. The surface area of the catalysts decreased gradually with increasing calcination temperature. The SCR activity of V2O5/ZrO2 catalysts was found to be related with the support crystallinity, whereas V2O5/CeO2–ZrO2 catalysts were also dependent...... on acidic and redox properties of the catalyst. The V2O5/CeO2–ZrO2 catalysts showed high activity and selectivity for reduction of NO with NH3....

Catalytic properties of pure and K{sup +}-doped Cu O/Mg O system towards 2-propanol conversion

Energy Technology Data Exchange (ETDEWEB)

El-Molla, S. A.; Amin, N. H.; Hammed, M. N.; Sultan, S. N. [Ain Shams University, Faculty of Education, Chemistry Department, Roxy, Heliopolis, Cairo 11757 (Egypt); El-Shobaky, G. A., E-mail: saharelmolla@yahoo.com [National Research Center, Dokki, Cairo (Egypt)

2013-08-01

Cu O/Mg O system having different compositions was prepared by impregnation method followed by calcination at 400-900 C. The effect of Cu O content, calcination temperature and doping with small amounts of K{sup +} species (1-3 mol %) on physicochemical, surface and catalytic properties of the system were investigated using X-ray diffraction, adsorption of N{sub 2} at - 196 C, and conversion of isopropyl alcohol at 150-400 C using a flow technique. The results revealed that the solids having the formulae 0.2 and 0.3 Cu O/Mg O calcined at 400 C consisted of nano sized Mg O and Cu O as major phases together with Cu{sub 2}O as minor phase. The Bet-surface areas of different absorbents are decreased by increasing Cu O content, calcination temperature and K{sup +}-doping. Mg O-support material showed very small catalytic activity in 2-propanol conversion. The investigated system behaved as selective catalyst for dehydrogenation of 2-propanol with selectivity >80%. The catalytic activity increased by increasing Cu O content and decreased by increasing the calcination temperature within 400-900 C. K{sup +}-doping increased the catalytic activity and catalytic durability. (Author)

Excitation energy transfer to luminescence centers in M{sup II}MoO{sub 4} (M{sup II}=Ca, Sr, Zn, Pb) and Li{sub 2}MoO{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Spassky, D.A., E-mail: deris2002@mail.ru [Skobeltsyn Institute of Nuclear Physics, M.V. Lomonosov Moscow State University, Leninskie Gory 1, bld.2, 119991 Moscow (Russian Federation); National University of Science and Technology (MISiS), Leninsky Prospekt 4, 119049 Moscow (Russian Federation); Kozlova, N.S. [National University of Science and Technology (MISiS), Leninsky Prospekt 4, 119049 Moscow (Russian Federation); Nagirnyi, V. [Institute of Physics, University of Tartu, W. Ostwaldi 1, 50411 Tartu (Estonia); Savon, A.E. [Skobeltsyn Institute of Nuclear Physics, M.V. Lomonosov Moscow State University, Leninskie Gory 1, bld.2, 119991 Moscow (Russian Federation); Hizhnyi, Yu.A.; Nedilko, S.G. [Taras Shevchenko National University of Kyiv, Volodymyrska str. 64/13, 01601 Kyiv (Ukraine)

2017-06-15

Based on the results of spectroscopy studies and electronic band structure calculations, the analysis of excitation energy transformation into luminescence is performed for a set of molybdates M{sup II}MoO{sub 4} (M{sup II}=Ca, Sr, Zn, Pb) and Li{sub 2}MoO{sub 4}. The bandgap energies were determined from comparison of experimental and calculated reflectivity spectra as 3.3 eV for PbMoO{sub 4}, 4.3 eV for ZnMoO{sub 4}, 4.4 eV for CaMoO{sub 4}, 4.7 eV for SrMoO{sub 4}, and 4.9 eV for Li{sub 2}MoO{sub 4}. It is shown that photoluminescence excitation spectra of these materials reveal the specific features of their conduction bands. The threshold of separated charge carriers’ creation is shown to be by 1.3–1.9 eV higher than the bandgap energy in CaMoO{sub 4}, SrMoO{sub 4} and ZnMoO{sub 4}. The effect is explained by the peculiarities of conduction band structure, namely to the presence of gap between the subbands of the conduction band and to the low mobility of electrons in the lower sub-band of the conduction band.

Investigation of chemical bond characteristics, thermal expansion coefficients and bulk moduli of alpha-R2MoO6 and R2Mo2O7 (R = rare earths) by using a dielectric chemical bond method.

Science.gov (United States)

Li, Huaiyong; Zhang, Siyuan; Zhou, Shihong; Cao, Xueqiang

2009-09-01

Theoretical researches are performed on the alpha-R2MoO6 (R = Y, Gd, Tb Dy, Ho, Er, Tm and Yb) and pyrochlore-type R2Mo2O7 (R = Y, Nd, Sm, Gd, Tb and Dy) rare earth molybdates by using chemical bond theory of dielectric description. The chemical bonding characteristics and their relationship with thermal expansion property and compressibility are explored. The calculated values of linear thermal expansion coefficient (LTEC) and bulk modulus agree well with the available experimental values. The calculations reveal that the LTECs and the bulk moduli do have linear relationship with the ionic radii of the lanthanides: the LTEC decreases from 6.80 to 6.62 10(-6)/K and the bulk modulus increases from 141 to 154 GPa when R goes in the order Gd, Tb Dy, Ho, Er, Tm, and Yb in the alpha-R2MoO6 series; while in the R2Mo2O7 series, the LTEC ranges from 6.80 to 6.61 10(-6)/K and the bulk modulus ranges from 147 to 163 GPa when R varies in the order Nd, Sm, Gd, Tb and Dy. Copyright 2008 Wiley Periodicals, Inc.

Synthesis of supported and unsupported NiMo carbides and their properties for the catalytic hydrocracking of n-octane

International Nuclear Information System (INIS)

Torre, A I Reyes de la; Banda, J A Melo; Alamilla, R GarcIa; Sandoval Robles, G; Rojas, E Terres; Lopez Ortega, A; Dominguez, J M

2004-01-01

Unsupported and γ-Al 2 O 3 -, MCM-41-supported (Ni, Mo) carbides were prepared and modified by 'in situ' polymer (PAN: polyacrylonitrile) pyrolysis. The supported catalysts were impregnated with Ni and Mo metals, i.e. 2.8 atom Mo/nm 2 , whose atomic ratio was Ni/Ni+Mo = 0.5. X-ray diffraction (XRD) showed single NiC, MoC phases in all cases, with relatively low surface areas, as verified by N 2 adsorption (BET). The catalytic behaviour of the supported (Ni, Mo)C phases for n-C 8 hydrocracking depended on the support type. (Ni, Mo)C/MCM41-PAN-P (P = pyrolyzed) showed a total conversion of 40% while it was only 15% on Ni,MoC/γ-Al 2 O 3 . The most active catalysts were (Ni, Mo)C unsupported catalysts, i.e., 90% total conversion. In all cases the hydrocracking selectivity favoured lighter hydrocarbons (C 1 -C 4 )

Raman spectrum, quantum mechanical calculations and vibrational assignments of (95% alpha-TeO2/5% Sm2O3) glass.

Science.gov (United States)

Shaltout, I; Mohamed, Tarek A

2007-06-01

Chozen system of tellurite glasses doped with rare earth oxides (95% alpha-TeO(2)+5% Sm2O3) was prepared by melt quenching. Consequently, the Raman spectrum (150-1250 cm(-1)) of the modified tellurite have been recorded. As a continuation to our normal coordinate analysis, force constants and quantum mechanical (QM) calculations for tbp TeO4(4-) (triagonal bipyramid, C(2v)) and TeO(3+1); Te2O7(6-) (bridged tetrahedral), we have carried out ab initio frequency calculations for tpy TeO3(2-) (triagonal pyramidal, C(3v) and C(s)) and tp TeO3(2-) (triagonal planar, D(3h)) ions. The quantum mechanical calculations at the levels of RHF, B3LYP and MP2 allow confident vibrational assignments and structural identification in the binary oxide glass (95% alpha-TeO2 +5% Sm2O3). The dominant three-dimensional network structures in the modified glass are triagonal pyramidal TeO3 with minor features of short range distorted tbp TeO4 and bridged tetrahedral unit of TeO(3+1), leading to a structure of infinite chain. Therefore, alpha-TeO2/Sm2O3 (95/5%) glass experience structural changes from TeO4 (tbp); Te2O7 (TeO(3+1))-->TeO3 (tpy).

Solid state reactions of MoO3 and Na2MoO4 with (U.85,Ce.15)O2x

International Nuclear Information System (INIS)

Dahale, N.D.; Keskar, Meera; Singh Mudher, K.D.; Chawla, K.L.

1999-01-01

(U .85 ,Ce .15 )MoO 6-x was prepared by the solid state reactions of (U .85 ,Ce .15 )O 2±x with MoO 3 in air at 600 deg C. Solid state reactions of Na 2 MoO 4 with (U .85 ,Ce .15 )MoO 6.x up to 550 deg C in air led to the formation of Na 2 (U .85 ,Ce .15 )Mo 2 O 10-x and Na 2 (U .85 , Ce .15 ) 2 Mo 3 O 16-x . These compounds were characterised by x-ray and thermal methods. The x-ray powder data of (U .85 , Ce .15 ) MoO 6-x were indexed on monoclinic system whereas, data of Na 2 (U .85 ,Ce .15 ) Mo 2 O 10-x and Na 2 (U .85 ,Ce .15 ) 2 Mo 3 O 16-x were indexed on orthorhombic and monoclinic system respectively. (author)

[Pd(NH{sub 3}){sub 4}]MoO{sub 4} as a precursor for Pd–Mo-containing catalysts: Thermal behavior, X-ray analysis of the thermolysis products and related catalytic studies

Energy Technology Data Exchange (ETDEWEB)

Gubanov, Alexander I., E-mail: gubanov@niic.nsc.su [Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences, Akad. Lavrentiev Prospekt 3, 630090 Novosibirsk (Russian Federation); Novosibirsk State University, Pirogova str. 2, 630090 Novosibirsk (Russian Federation); Filatov, Eugeny Yu.; Semitut, Eugeny Yu.; Smolentsev, Anton I. [Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences, Akad. Lavrentiev Prospekt 3, 630090 Novosibirsk (Russian Federation); Novosibirsk State University, Pirogova str. 2, 630090 Novosibirsk (Russian Federation); Snytnikov, Pavel V.; Potemkin, Dmitry I. [Novosibirsk State University, Pirogova str. 2, 630090 Novosibirsk (Russian Federation); Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Akad. Lavrentiev Prospekt 5, 630090 Novosibirsk (Russian Federation); Korenev, Sergey V. [Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences, Akad. Lavrentiev Prospekt 3, 630090 Novosibirsk (Russian Federation); Novosibirsk State University, Pirogova str. 2, 630090 Novosibirsk (Russian Federation)

2013-08-20

Highlights: • [Pd(NH{sub 3}){sub 4}]MoO{sub 4} as a precursor for Pd–Mo-containing catalysts. • Different products are formed depending on atmosphere of thermal decomposition. • Thermolysis in He atmosphere affords finely mixed two-phase nanosized system Pd–MoO{sub 2}. • Pd–MoO{sub 2} system can be a promising catalyst both in pure and supported form. - Abstract: Compound [Pd(NH{sub 3}){sub 4}]MoO{sub 4} (1) has been synthesized and characterized by IR spectroscopy, analytical data, powder and single-crystal X-ray crystallography. Thermal properties of 1 have been examined by thermogravimetry. Powder X-ray diffraction has been applied to investigate the nanosized products of thermal decomposition of the precursor in hydrogen (Pd–Mo) and helium (Pd–MoO{sub 2}) atmospheres. Pd–Mo catalysts supported with γ-Al{sub 2}O{sub 3} have been tested in oxidation of CO and H{sub 2} mixtures.

Syntheses, structures, and properties of Ag4(Mo2O5)(SeO4)2(SeO3) and Ag2(MoO3)3SeO3

International Nuclear Information System (INIS)

Ling Jie; Albrecht-Schmitt, Thomas E.

2007-01-01

Ag 4 (Mo 2 O 5 )(SeO 4 ) 2 (SeO 3 ) has been synthesized by reacting AgNO 3 , MoO 3 , and selenic acid under mild hydrothermal conditions. The structure of this compound consists of cis-MoO 2 2+ molybdenyl units that are bridged to neighboring molybdenyl moieties by selenate anions and by a bridging oxo anion. These dimeric units are joined by selenite anions to yield zigzag one-dimensional chains that extended down the c-axis. Individual chains are polar with the C 2 distortion of the Mo(VI) octahedra aligning on one side of each chain. However, the overall structure is centrosymmetric because neighboring chains have opposite alignment of the C 2 distortion. Upon heating Ag 4 (Mo 2 O 5 )(SeO 4 ) 2 (SeO 3 ) looses SeO 2 in two distinct steps to yield Ag 2 MoO 4 . Crystallographic data: (193 K; MoKα, λ=0.71073 A): orthorhombic, space group Pbcm, a=5.6557(3), b=15.8904(7), c=15.7938(7) A, V=1419.41(12), Z=4, R(F)=2.72% for 121 parameters with 1829 reflections with I>2σ(I). Ag 2 (MoO 3 ) 3 SeO 3 was synthesized by reacting AgNO 3 with MoO 3 , SeO 2 , and HF under hydrothermal conditions. The structure of Ag 2 (MoO 3 ) 3 SeO 3 consists of three crystallographically unique Mo(VI) centers that are in 2+2+2 coordination environments with two long, two intermediate, and two short bonds. These MoO 6 units are connected to form a molybdenyl ribbon that extends along the c-axis. These ribbons are further connected together through tridentate selenite anions to form two-dimensional layers in the [bc] plane. Crystallographic data: (193 K; MoKα, λ=0.71073 A): monoclinic, space group P2 1 /n, a=7.7034(5), b=11.1485(8), c=12.7500(9) A, β=105.018(1) V=1002.7(2), Z=4, R(F)=3.45% for 164 parameters with 2454 reflections with I>2σ(I). Ag 2 (MoO 3 ) 3 SeO 3 decomposes to Ag 2 Mo 3 O 10 on heating above 550 deg. C. - Graphical abstract: A view of the one-dimensional [(Mo 2 O 5 )(SeO 4 ) 2 (SeO 3 )] 4- chains that extend down the c-axis in the structure of Ag 4 (Mo 2 O 5 )(SeO 4

XAS study of V2O5/Al2O3 catalysts doped with rare earth oxides

International Nuclear Information System (INIS)

Centeno, M.A.; Malet, P.; Capitan, M.J.; Benitez, J.J.; Carrizosa, I.; Odriozola, J.A.

1995-01-01

This paper reports on XAS studies of well dispersed V 2 O 5 /Al 2 O 3 and V 2 O 5 /Sm 2 O 3 /Al 2 O 3 samples. XAS spectra at V-K and Sm-L III edges show that the rare earth oxide favours the formation of regular tetrahedral units, [VO 4 ], over the surface of the support. Positions of the preedge peak at the V-K edge, and intensities of the white line at the Sm-L III edge also suggest modifications in the electronic density around V and Sm atoms when they are simultaneously supported over Al 2 O 3 . ((orig.))

Tailoring the luminescence properties of Y_2O_3:Sm"3"+ nanophosphors by 6 MeV electron beam irradiation

International Nuclear Information System (INIS)

Sunitha, D.V.; Nagabhushana, H.; Hareesh, K.; Bhoraskar, V.N.; Dhole, S.D.

2017-01-01

Sm"3"+ (3 mol%) ions doped Y_2O_3 nanophosphors were synthesized by green synthesis route using Aloe Vera gel as fuel. The final product was irradiated by 6 MeV electron beam (E-beam) to different fluences in the range (2–10 × 10"1"3 e"− cm"−"2) and well characterized. Powder X-ray Diffractogram (PXRD) results revealed the loss of crystalline nature due to lattice disorder created during irradiation. Fourier Transform Infrared (FTIR) spectroscopic results showed absorption peaks around 688–843 cm"−"1 (Y-O bond), 1076 and 1398 cm"−"1 (C-O bond), 1505–1765 cm"−"1 and 3498 cm"−"1 (O-H bond). Scanning Electron Microscopic (SEM) images showed flake like morphological features. The Photoluminescence (PL) emission spectrum recorded at 407 nm excitation showed magnetic and electric dipole transitions at ∼569–575 ("4G_5_/_2 → "6H_5_/_2), ∼607–623 ("4G_5_/_2 → "6H_7_/_2) and ∼655–668 nm ("4G_5_/_2 → "6H_9_/_2) respectively. Thermoluminescence (TL) glow curve consists of three peaks in E-beam irradiated nanophosphors at 158, 243 and 352 °C due to creation of more number of trapping and luminescent centers. The E-beam irradiated Y_2O_3:Sm"3"+ nanophosphors showed strong PL emission with color co-ordinate values lying in the orange-red region. Therefore, this material can be potentially used as a red component in WLEDs (White LEDs). - Highlights: • Y_2O_3:Sm"3"+ nanophosphor was synthesized by solution combustion technique using Aloe Vera gel as a fuel. • Y_2O_3:Sm"3"+ nanophosphor was irradiated with 6 MeV E-beam in the fluence range 2–10 × 10"1"3e"− cm"−"2. • The size of the particle decreases and surface area increases with increase in E-beam fluence. • The E-beam irradiated Y_2O_3:Sm"3"+ nanophosphors PL intensity increases and CIE coordinate values moves towards red region indicating the potential usage of this phosphor for LED applications.

Mass spectrometric determination of stability of gaseous BaMoO2, Ba2MoO4, Ba2MoO5, Ba2Mo2O8 molecules

International Nuclear Information System (INIS)

Kudin, L.S.; Balduchchi, Dzh.; Dzhil'i, G.; Gvido, M.

1982-01-01

During the mass spectrometric investigation of BaCrO 4 evaporation Cr + , Ba + , BaO + main ions are recorded as well as BaMoO 4 + , BaMoO 3 + , BaMoO 2 + , BaMoO + , BaMoO 4 + , Ba 2 MoO 5 + , BaMo 2 O 8 + ions - the products of ionization of three-component (Ba, Mo, M) molecules, forming as a result of substance chemical interaction with the material of an effusion cell (Mo). Heats of formation of BaMoO 2 , Ba 2 MoO 4 , Ba 2 MoO 5 and Ba 2 Mo 2 O 8 molecules which constituted - 577+-70, -1343+-115, -1464+-70, -2393+-90 k J/mol respectively are determined on the base of the analysis of curves of ionisation efficiency and of reaction heats Ba 2 MoO 5 =BaO+BaMoO 4 , ΔH 0 0 =322+-60 kJ/mol Ba 2 Mo 2 O 8 =2BaMoO 4 , ΔH 0 0 =351+-80 kJ/mol calculated with the use of third low of thermodynamics [ru

Combustion synthesis and characterization of MV0.5P0.5O4: Sm3+, Tm3+ (M = Gd, La, Y)

Science.gov (United States)

Motloung, Selepe J.; Lephoto, Mantwa A.; Tshabalala, Kamohelo G.; Ntwaeaborwa, Odireleng M.

2018-04-01

In this paper, GdV0.5P0.5O4: Sm3+, Tm3+, LaV0.5P0.5O4: Sm3+, Tm3+ and YV0.5P0.5O4: Sm3+, Tm3+ phosphor powders were prepared by solution combustion method using urea as a fuel. The phase purity, surface morphology, optical and photoluminescence properties were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-vis spectroscopy and photoluminescence spectroscopy. The XRD results indicated that the prepared powders are of a single phase and crystallized in tetragonal structure for Gd and Y systems while monoclinic phase was observed for La system. SEM showed that the samples consisted of mixed structures. The estimated band gaps were 2.2, 2.4 and 2.3 eV for Y, Gd and La systems respectively. The photoluminescence results showed four emission peaks. One peak is assigned to 1G4 - 3H6 transition of Tm3+, and three other emission peaks are attributed to 6G5/2 - 6H5/2, 6G5/2 - 6H7/2 and 6G5/2 - 6H9/2 transitions of Sm3+. The photoluminescent intensity was the highest in the gadolinium system.

Phase formation in the Ag2O - MgO - MoO3 system and the crystal structure of new double molybdate Ag2Mg2(MoO4)3

International Nuclear Information System (INIS)

Tsyrenova, G.D.; Khajkina, E.G.; Khobrakova, Eh.T.; Solodovnikov, S.F.

2001-01-01

The phase correlations in subsolidus area of the Ag 2 O - MgO - MoO 3 system were studied, the Ag 2 MoO 4 - MgMoO 4 polythermal cross-section was investigated and its T-x diagram was constructed. X-ray diffraction and thermal analytic researches were conducted. The formation of the new double Ag 2 Mg 2 (MoO 4 ) 3 molybdates relating to the structural group Na 2 Mg 5 (MoO 4 ) 6 was established, and its structure (a=6.978(1), b=8.715(2), c=10.294(2) A, α=107.56(3) Deg, β=105.11(3) Deg, γ=103.68(3) Deg, Z=2, sp. gr. P 1-bar, R=0.038) was determined. The mixed carcass from the twin MgO 6 -octahedrons and MoO 4 -tetrahedrons, in which blankness the Ag atoms are arranged, stand out in the structure.The character of disordering in the part of Ag + is analogous to previously found one in the Ag 2 Zn 2 (MoO 4 ) 3 structure. The possible limits in the fields of homogeneity of silver-magnesium molybdate and its analogs, as well as the differences their structure from the structure of isotopic sodium-containing phases, are discussed [ru

A study of the Fe-based superconductor SmFeAsO{sub 1-x}F{sub x} by x-ray photoelectron spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Zhang, Y; Chen, Y L; Cui, Y J; Cheng, C H; Zhao, Y [Key Laboratory of Magnetic Levitation Technologies and Maglev Trains (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Zhang, H [Department of Physics, Peking University, Beijing 100871 (China)], E-mail: yzhao@swjtu.edu.cn

2009-01-15

The electronic structure of the Fe-based superconductor SmFeAsO{sub 1-x}F{sub x} (x = 0 and 0.2) is studied with x-ray photoemission spectroscopy (XPS) through comparing the band structures of the nonsuperconducting parent material SmFeAsO and the superconducting SmFeAsO{sub 0.8}F{sub 0.2} (T{sub c} = 52.5 K). A small peak centered at 0.2 eV below the Fermi level, E{sub F}, in the valence band is observed in the parent material SmFeAsO, which is due to the low-spin state of the Fe 3d electrons. With fluorine doping, the peak at 0.2 eV disappears and a broad plateau forms near the Fermi level; in the meantime, the density of states at E{sub F} is slightly suppressed. The O 1s and Sm 3d core levels shift towards high energy by {approx}0.55 eV with fluorine doping, but in a sharp comparison, the Fe 2p and As 3d core levels do not shift significantly (the binding energy shift is less than 0.01 eV). It is deduced from the core-level shifts that the Fermi level of the system moves up by 0.55 eV by fluorine doping.

Effect of Calcination Temperatures and Mo Modification on Nanocrystalline (γ-χ-Al2O3 Catalysts for Catalytic Ethanol Dehydration

Directory of Open Access Journals (Sweden)

Tharmmanoon Inmanee

2017-01-01

Full Text Available The mixed gamma and chi crystalline phase alumina (M-Al catalysts prepared by the solvothermal method were investigated for catalytic ethanol dehydration. The effects of calcination temperatures and Mo modification were elucidated. The catalysts were characterized by X-ray diffraction (XRD, N2 physisorption, transmission electron microscopy (TEM, and NH3-temperature programmed desorption (NH3-TPD. The catalytic activity was tested for ethylene production by dehydration reaction of ethanol in gas phase at atmospheric pressure and temperature between 200°C and 400°C. It was found that the calcination temperatures and Mo modification have effects on acidity of the catalysts. The increase in calcination temperature resulted in decreased acidity, while the Mo modification on the mixed phase alumina catalyst yielded increased acidity, especially in medium to strong acids. In this study, the catalytic activity of ethanol dehydration to ethylene apparently depends on the medium to strong acid. The mixed phase alumina catalyst calcined at 600°C (M-Al-600 exhibits the complete ethanol conversion having ethylene yield of 98.8% (at 350°C and the Mo-modified catalysts promoted dehydrogenation reaction to acetaldehyde. This can be attributed to the enhancement of medium to strong acid with metal sites of catalyst.

Compounds of type Ba/sub 2/Bsup(III)Ossup(V)O/sub 6/

Energy Technology Data Exchange (ETDEWEB)

Treiber, U; Kemmler-Sack, S [Tuebingen Univ. (Germany, F.R.). Lehrstuhl fuer Anorganische Chemie 2

1981-07-01

The black perovskites of type Ba/sub 2/Bsup(III)Ossup(V)O/sub 6/ crystallize cubic (Bsup(III) = Pr, Nd, Sm-Lu, Y) and rhombohedral (Bsup(III) = La) respectively; the cell volumina decrease linearily with (rsub(B)sup(III))/sup 3/. Intensity calculations on powder data for Ba/sub 2/YOsO/sub 6/ (space group Fm3m-Osub(h)/sup 5/) and Ba/sub 2/LaOsO/sub 6/ (space group R-3m-Dsub(3d)/sup 5/) gave the intensity related R'values of 4.6% and 5.0% respectively. The results of the vibrational spectroscopic investigations are reported in common with the bond orders, M-O distances and mean amplitudes and compared with the corresponding values of the series Ba/sub 2/Bsup(III)Irsup(V)O/sub 6/ and Ba/sub 2/Bsup(III)Rusup(V)O/sub 6/.

Preparation, Characterization, and Catalytic Activity of MoCo/USY Catalyst on Hydrodeoxygenation Reaction of Anisole

Science.gov (United States)

Nugrahaningtyas, K. D.; Suharbiansah, R. S. R.; Rahmawati, F.

2018-03-01

This research aims to prepare, characterize, and study the catalytic activity of Molybdenum (Mo) and Cobalt (Co) metal with supporting material Ultra Stable Y-Zeolite (USY), to produce catalysts with activity in hydrotreatment reaction and in order to eliminate impurities compounds that containing unwanted groups heteroatoms. The bimetallic catalysts MoCo/USY were prepared by wet impregnation method with weight variation of Co metal 0%, 2%, 4%, 6%, 8%, and Mo metal 8% (w/w), respectively. Activation method of the catalyst included calcination, oxidation, reduction and the crystallinity was characterized using X-ray diffraction (XRD), the acidity of the catalyst was analyzed using Fourier Transform Infrared Spectroscopy (FT-IR) and gravimetry method, minerals present in the catalyst was analyzed using X-Ray Fluorescence (XRF), and surface of the catalyst was analyzed using Surface Area Analyzer (SAA). Catalytic activity test (benzene yield product) of MoCo/USY on hydrodeoxigenation reaction of anisole aimed to determine the effect of Mo-Co/USY for catalytic activity in the reaction hydrodeoxigenation (HDO) anisole. Based on characterization and test of catalytic activity, it is known that catalytic of MoCo/USY 2% (catalyst B) shows best activities with acidity of 10.209 mmol/g, specific area of catalyst of 426.295 m2/g, pore average of 14.135 Å, total pore volume 0.318 cc/g, and total yield of HDO products 6.06%.

Synthesis, characterization and antimicrobial activity of some nitrilotriacetic acid−V(III, −Sn(II, −Sm(II and −Sm(III complexes

Directory of Open Access Journals (Sweden)

Mohsen S. Asker

2011-04-01

Full Text Available Four new complexes [V(NTA(H2O 2]•H2O (1, H[Sn(NTA] (2, H[Sm(NTA]•H2O (3, and [Sm(NTA(H2O 2]•H2O (4 were obtained during the reactions of metal salts (VCl3, SnCl2•2H2O, SnCl4, Sm(NO32•6H2O and SmCl3•6H2O with nitrilotriacetic acid, H3NTA. The infrared and 1H-NMR spectra of the solid complexes have been obtained and assigned. Thermogravimetric analyses were also carried out. The data obtained agree with the proposed structures and show that the complexes decomposed to the corresponding metal oxide. The ligand and their metal complexes were screened for their antimicrobial activities by the agar-well diffusion technique using DMSO as a solvent against the following bacterial species: Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa and antifungal activity against Aspergillus niger, Aspergillus flavus, Saccharomyces cerevisiae and Candida albicans. The obtained results were compared with some types of known antibiotics. The minimum inhibitory concentration (MIC values were calculated at 30 °C for 24−48 h. The activity data show that the complexes are more potent antimicrobials than the parent ligand.

Detection of hydrogen peroxide and glucose by using Tb2(MoO4)3 nanoplates as peroxidase mimics

Science.gov (United States)

Rahimi-Nasrabadi, Mehdi; Mizani, Farhang; Hosseini, Morteza; Keihan, Amir Homayoun; Ganjali, Mohammad Reza

2017-11-01

Tb2(MoO4)3 nanostructures are demonstrated for the first time to have an intrinsic peroxidase-like activity. Tb2(MoO4)3 nanoplates could efficiently catalyse the oxidation of 3,3‧,5,5‧-tetramethylbenzidine (TMB) to generate a blue dye (with an absorbance maximum at 652 nm) in the presence of H2O2. Based on the highly efficient catalytic of Tb2(MoO4)3 nanoplates, a novel system for optical determination of H2O2 and glucose was successfully established under optimized conditions. The assay had 0.0.08 μM and 0.1 μM detection limit for H2O2 and glucose, respectively. In our opinion, this enzyme mimetic has a potential to use in other oxidase based assays.

Selective oxidation of i-butene and i-butene to methacrolein and methacrylic acid over Keggin-type polyoxometalate and MoVTeNbOx catalysts. A comparative catalytic and in situ-spectroscopic study

Energy Technology Data Exchange (ETDEWEB)

Bentrup, U.; Brueckner, A.; Kant, M.; Kolf, S.; Dingerdissen, U. [Institut fuer Angewandte Chemie Berlin-Adlershof e.V. (Germany); Jansen, S.; Maschmeyer, D.; Sieger, H.; Zanthoff, H.W. [Degussa AG, Marl (Germany)

2005-07-01

An alternative to overcome the drawbacks connected with POM catalysts may be the development of suitable mixed metal oxide catalysts. MoVTeNbO{sub x} materials could be promising candidates since they revaled remarkable performance in the selective oxidation of propane to acrylic acid. However, up to now their behaviour in the selective oxidation of i-butane has rarely been studied. The investigations presented in this paper are focused on the interaction of feed components (i-butane / i-butene, O{sub 2}, H{sub 2}O) with Keggin-type polyoxometalate and MoVTeNbO{sub x} catalysts. FTIR spectroscopy was used to identify adsorbed intermediates and products while the novel simultaneous operando-EPR/UV-vis/Raman/GC technique revealed to be an excellent tool to follow the behaviour of V and Mo sites. In relation to the results of catalytic tests, structure-reactivity relationships are derived. (orig.)

Studies on the phase diagram of Pb-Mo-O system

International Nuclear Information System (INIS)

Aiswarya, P.M.; Ganesan, Rajesh; Gnanasekaran, T.

2014-01-01

Liquid lead and Lead-Bismuth Eutectic (LBE) alloy are considered as spallation target and coolant in the accelerator driven systems and as candidate coolant in advanced nuclear reactors. Corrosion of the structural steel components in these liquid metal coolants can be minimized by the insitu formation of passive oxide layer on the steel surface under controlled oxygen concentration. A detailed knowledge of phase diagrams of Pb-M-O and Bi-M-O (M = Fe, Cr, Mo) systems and data on thermochemical properties of the ternary compounds of these systems are required for better understanding of composition and stability of these passive oxide films. In the present work, studies have been carried out to establish the ternary phase diagram of Pb-Mo-O system

Effect of Mo-Doped Mesoporous Al-SSP Catalysts for the Catalytic Dehydration of Ethanol to Ethylene

Directory of Open Access Journals (Sweden)

Titinan Chanchuey

2016-01-01

Full Text Available The catalytic dehydration of ethanol to ethylene over the mesoporous Al-SSP and Mo-doped Al-SSP catalysts was investigated. The Al-SSP catalyst was first synthesized by the modified sol-gel method and then doped with Mo by impregnation to obtain 1% Mo/Al-SSP and 5% Mo/Al-SSP catalysts (1 and 5 wt% of Mo. The final catalysts were characterized using various techniques such as XRD, N2 physisorption, SEM/EDX, TEM, and NH3-TPD. The catalytic activity for all catalysts in gas-phase ethanol dehydration reaction was determined at temperature range of 200°C to 400°C. It was found that the most crucial factor influencing the catalytic activities appears to be the acidity. The acid property of catalysts depended on the amount of Mo loading. Increased Mo loading in Al-SSP resulted in increased weak acid sites, which enhanced the catalytic activity. Besides acidity, the high concentration of Al at surface of catalyst is also essential to obtain high activity. Based on the results, the most suitable catalyst in this study is 1% Mo/Al-SSP catalyst, which can produce ethylene yield of ca. 90% at 300°C with slight amounts of diethyl ether (DEE and acetaldehyde.

MoO3/Al2O3 catalyst: Comparison of catalysts prepared by new slurry impregnation with molybdic acid with conventional samples

International Nuclear Information System (INIS)

Spojakina, A.; Kostova, N.; Vit, Z.; Zdrazil, M.

2003-01-01

Alumina-supported molybdena catalysts were prepared by conventional impregnation with (NH 4 ) 6 Mo 7 O 24 (CIM) and by a new slurry impregnation method (SIM). SIM is the reaction of alumina support with a slurry of MoO 3 in water. Two commercial supports were used and the commercial Mo 3 /Al 2 O 3 catalyst was included for comparison. Maximum amount of MoO 3 deposited by SIM was about 19-20 % MoO 3 with the surface area of the support of 260-280 m 2 g -1 and this corresponded to saturation monolayer of similar density as described in literature for CIM catalysts. At the ratios of MoO 3 to Al 2 O 3 in the impregnation slurry below saturation monolayer, the pH of the slurry was 3.5-6 (depending on loading) and chemical erosion of alumina is negligible. However, using the large excess of MoO 3 (35% MoO 3 ) the pH was 2.4-3.4 and chemical erosion of alumina occurred. Silica contained in alumina supports was partly extracted as soluble silicomolybdic anions during SIM. The catalysts were characterized by BET, IR, DRS (UV-vis and NIR), TPR and catalytic activity in hydrodesulfurization of thiophene. Calcination had no significant effect on the properties of SIM catalysts and this proved that calcination is not needed in that method. All catalysts exhibited features of high monolayer dispersion of molybdena and no significant difference in structure and catalytic properties was observed between SIM and CIM catalysts. This confirmed that SIM is a simple, clean and reliable method of preparation of monolayer type MoO 3 /Al 2 O 3 catalysts. (author)

Probing edge-activated resonant Raman scattering from mechanically exfoliated 2D MoO3 nanolayers

International Nuclear Information System (INIS)

Yano, Taka-aki; Yoshida, Keisuke; Hayashi, Tomohiro; Hara, Masahiko; Hayamizu, Yuhei; Ohuchi, Fumio

2015-01-01

We report spatially resolved vibrational analysis of mechanically exfoliated single-crystalline α-MoO 3 nanolayers. Raman scattering from α-MoO 3 was enhanced predominantly at the outside edges of the nanolayers. The enhanced Raman scattering at the edges was attributed primarily to the enhanced resonant Raman effect caused by a high density of oxygen vacancies localized at the edges. The localized vacancy sites corresponded to a non-stoichiometric phase of MoO 3 , which would provide reactive sites with high catalytic activity. (paper)

Thermal expansion of Cr2xFe2-2xMo3O12, Al2xFe2-2xMo3O12 and Al2xCr2-2xMo3O12 solid solutions

International Nuclear Information System (INIS)

Ari, M.; Jardim, P.M.; Marinkovic, B.A.; Rizzo, F.; Ferreira, F.F.

2008-01-01

The transition temperature from monoclinic to orthorhombic and the thermal expansion of the orthorhombic phase were investigated for three systems of the family A 2 M 3 O 12 : Cr 2x Fe 2-2x Mo 3 O 12 , Al 2x Fe 2-2x Mo 3 O 12 and Al 2x Cr 2-2x Mo 3 O 12 . It was possible to obtain a single-phase solid solution in all studied samples (x=0, 0.1, 0.3, 0.5, 0.7, 0.9 and 1). A linear relationship between the transition temperature and the fraction of A 3+ cations (x) was observed for each system. In all orthorhombic solid solutions studied here the observed thermal expansion was anisotropic. These anisotropic thermal expansion properties of crystallographic axes a, b and c result in a low positive or near-zero overall linear coefficient of thermal expansion (α l =α V /3). The relationship between the size of A 3+ cations in A 2 M 3 O 12 and the coefficient of thermal expansion is discussed. Near-zero thermal expansion of Cr 2 Mo 3 O 12 is explained by the behavior of Cr-O and Mo-O bond distances, Cr-Mo non-bond distances and Cr-O-Mo bond angles with increasing temperature, estimated by Rietveld analysis of synchrotron X-ray powder diffraction data. - Graphical abstract: In this figure, all published overall linear coefficients of thermal expansion for orthorhombic A 2 M 3 O 12 family obtained through diffraction methods as a function of A 3+ cation radii size, together with dilatometric results, are plotted. Our results indicate that Cr 2 Mo 3 O 12 does not exactly follow the established relationship

Preparation and characterization of Bi26-2xMn2xMo10O69-d and Bi26.4Mn0.6Mo10-2yMe2yO69-d (Me = V, Fe Solid Solutions

Directory of Open Access Journals (Sweden)

Z. A. Mikhaylovskaya

2017-09-01

Full Text Available Single phase samples of bismuth molybdate, Bi26Mo10O69, doped with Mn on the bismuth sublattice and V, Fe on the molybdenum sublattice were found to crystallize in the triclinic Bi26Mo10O69 structure at low doping levels and in the monoclinic Bi26Mo10O69 structure - at higher dopant concentration. The assumption that all Mn ions have an oxidation state of +2 was confirmed by means of magnetic measurement results analysis using Curie-Weiss law. Conductivity was investigated using impedance spectroscopy. The conductivity of Bi26.4Mn0.6Mo9.6Fe0.4O69-d was 1.2*10-2 S*cm-1 at 973 K and 2.2*10-4 S*cm-1 at 623 K, and the conductivity of Bi26.4Mn0.6Mo9.2V0.8O69-d was 2.2*10-3 S*cm-1 at 973 K and 2.2*10-5 S*cm-1 at 623 K.

Thermal expansion studies on UMoO5, UMoO6, Na2U(MoO4)3 and Na4U(MoO4)4

International Nuclear Information System (INIS)

Keskar, Meera; Dahale, N.D.; Krishnan, K.

2009-01-01

In the present work, thermal expansion behavior of lower valent sodium uranium molybdates, i.e., Na 2 U(MoO 4 ) 3 and Na 4 U(MoO 4 ) 4 were studied under vacuum in the temperature range of 298-873 K using high temperature X-ray diffractometry (HTXRD). Expansion behaviors of UMoO 5 and UMoO 6 were also studied in vacuum from 298 to 873 K and 773 K, respectively. UMoO 5 was synthesized by reacting UO 2 with MoO 3 in equi-molar proportion in evacuated sealed quartz ampoule at 1173 K for 14 h. Na 2 U(MoO 4 ) 3 and Na 4 U(MoO 4 ) 4 were prepared by reacting UMoO 5 and MoO 3 with 1 and 2 moles of Na 2 MoO 4 , respectively, at 873 K in evacuated sealed quartz ampoule. XRD data of UMoO 5 and UMoO 6 were indexed on orthorhombic and monoclinic systems, respectively, whereas, the data of Na 2 U(MoO 4 ) 3 and Na 4 U(MoO 4 ) 4 were indexed on tetragonal system. The lattice parameters and cell volume of all the four compounds, fit into polynomial expression with respect to temperature, showed positive thermal expansion (PTE) up to 873 K.

(18)O(2) label mechanism of sulfur generation and characterization in properties over mesoporous Sm-based sorbents for hot coal gas desulfurization.

Science.gov (United States)

Liu, B S; Wan, Z Y; Wang, F; Zhan, Y P; Tian, M; Cheung, A S C

2014-02-28

Using a sol-gel method, SmMeOx/MCM-41 or SBA-15 (Me=Fe, Co and Zn) and corresponding unsupported sorbents were prepared. The desulfurization performance of these sorbents was evaluated over a fixed-bed reactor and the effects of reaction temperature, feed and sorbent composition on desulfurization performance were studied. Samarium-based sorbents used to remove H2S from hot coal gas were reported for the first time. The results of successive sulfidation/regeneration cycles revealed that SmFeO3/SBA-15 sorbent was suitable for desulfurization of hot coal gas in the chemical industry. The formation of elemental sulfur during both sulfidation and regeneration processes depended strongly on the catalytic action of Sm2O2S species, which was confirmed for the first time via high sensitive time of flight mass spectrometer (TOF-MS) using 6%vol(18)O2/Ar regeneration gas and can reduce markedly procedural complexity. The sorbents were characterized using N2-adsorption, high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), temperature-programmed reduction of H2 (H2-TPR), thermogravimetry (TG) and time-of-flight mass spectrometry (TOF-MS) techniques. Copyright © 2014 Elsevier B.V. All rights reserved.

Low temperature preparation and superconductivity of F-doped SmFeAsO

Energy Technology Data Exchange (ETDEWEB)

Chen, Y.L.; Cui, Y.J. [Key Laboratory of Magnetic Levitation Technologies and Maglev Trains (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Cheng, C.H. [School of Materials Science and Engineering, University of New South Wales, Sydney, 2052 NSW (Australia); Yang, Y.; Wang, L.; Li, Y.C.; Zhang, Y. [Key Laboratory of Magnetic Levitation Technologies and Maglev Trains (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); Zhao, Y., E-mail: yzhao@swjtu.edu.c [Key Laboratory of Magnetic Levitation Technologies and Maglev Trains (Ministry of Education of China), Superconductivity R and D Center (SRDC), Mail Stop 165, Southwest Jiaotong University, Chengdu, Sichuan 610031 (China); School of Materials Science and Engineering, University of New South Wales, Sydney, 2052 NSW (Australia)

2010-11-01

A low temperature (1100 deg. C) process of preparing F-doped SmFeAsO samples has been developed using SmF{sub 3} with nanometer scale as the source of fluorine. A series of the SmFeAsO{sub 1-x}F{sub x} (x = 0, 0.05, 0.1, 0.15, 0.2, 0.25, 0.3) samples have been prepared using the present method. Compared with previous reports, the present SmF{sub 3} is more effective to introduce F into SmFeAsO system in which a transition temperature of 39 K can be observed when x = 0.05. The superconductivity is definitely enhanced with the increasing F-doping level. All the samples presented to be layered structure and the crystal particle size is about three times larger with sintering time increasing from 36 h to 48 h. Except for the nanometer scale of SmF{sub 3}, the flux effect of SmF{sub 3} is recognized to be another reason for the decrease of the sintering temperature. Further more, a relatively large amount of SmF{sub 3} was also employed in the raw materials to introduce excessive F and this has induced higher T{sub c} (55 K) in SmFeAsO{sub 0.8}F{sub 0.2+{delta}}system.

Solid solutions in the system Nd2(SeO4)3 - Sm2(SeO4)3 - H2O

International Nuclear Information System (INIS)

Serebrennikov, V.V.; Tsybukova, T.N.; Velikov, A.A.

1984-01-01

Using the method of isothermal solubility at 25 deg C the system Nd 2 (SeO 4 ) 3 -Sm 2 (SeO 4 ) 3 -H 2 O has been studied. Roentgenographic recording of solid ''residues'' is realized. For solid solutions energies of interchange and formation heats are calculated. Formation heats of solid solutions on the basis of samarium selenates are also found experimentally

99Mo Yield Using Large Sample Mass of MoO3 for Sustainable Production of 99Mo

Science.gov (United States)

Tsukada, Kazuaki; Nagai, Yasuki; Hashimoto, Kazuyuki; Kawabata, Masako; Minato, Futoshi; Saeki, Hideya; Motoishi, Shoji; Itoh, Masatoshi

2018-04-01

A neutron source from the C(d,n) reaction has the unique capability of producing medical radioisotopes such as 99Mo with a minimum level of radioactive waste. Precise data on the neutron flux are crucial to determine the best conditions for obtaining the maximum yield of 99Mo. The measured yield of 99Mo produced by the 100Mo(n,2n)99Mo reaction from a large sample mass of MoO3 agrees well with the numerical result estimated with the latest neutron data, which are a factor of two larger than the other existing data. This result establishes an important finding for the domestic production of 99Mo: approximately 50% of the demand for 99Mo in Japan could be met using a 100 g 100MoO3 sample mass with a single accelerator of 40 MeV, 2 mA deuteron beams.

Shape-selective synthesis of Sn(MoO4)2 nanomaterials for catalysis and supercapacitor applications.

Science.gov (United States)

Sakthikumar, K; Ede, Sivasankara Rao; Mishra, Soumyaranjan; Kundu, Subrata

2016-06-07

Size and shape-selective Sn(MoO4)2 nanomaterials have been synthesized for the first time using a simple hydrothermal route by the reaction of Sn(ii) chloride salt with sodium molybdate in CTAB micellar media under stirring at 60 °C temperature for about three hours. Needle-like and flake-like Sn(MoO4)2 nanomaterials were synthesized by optimizing the CTAB to metal salt molar ratio and by controlling other reaction parameters. The eventual diameter and length of the nanoneedles are ∼100 ± 10 nm and ∼850 ± 100 nm respectively. The average diameter of the flakes is ∼250 ± 50 nm. The synthesized Sn(MoO4)2 nanomaterials can be used in two potential applications, namely, catalytic reduction of nitroarenes and as an anodic material in electrochemical supercapacitors. From the catalysis study, it was observed that the Sn(MoO4)2 nanomaterials could act as a potential catalyst for the successful photochemical reduction of nitroarenes into their respective aminoarenes within a short reaction time. From the supercapacitor study, it was observed that the Sn(MoO4)2 nanomaterials of different shapes show different specific capacitance (Cs) values and the highest Cs value was observed for Sn(MoO4)2 nanomaterials having a flake-like morphology. The highest Cs value observed was 109 F g(-1) at a scan rate of 5 mV s(-1) for the flake-like Sn(MoO4)2 nanomaterials. The capacitor shows an excellent long cycle life along with 70% retention of the Cs value, even after 4000 consecutive cycles at a current density of 8 mA cm(-2). Other than the applications in catalysis and supercapacitors, the synthesized nanomaterials can find further applications in photoluminescence, sensor and other energy-related devices.

Mapping Catalytically Relevant Edge Electronic States of MoS2

Science.gov (United States)

2018-01-01

Molybdenum disulfide (MoS2) is a semiconducting transition metal dichalcogenide that is known to be a catalyst for both the hydrogen evolution reaction (HER) as well as for hydro-desulfurization (HDS) of sulfur-rich hydrocarbon fuels. Specifically, the edges of MoS2 nanostructures are known to be far more catalytically active as compared to unmodified basal planes. However, in the absence of the precise details of the geometric and electronic structure of the active catalytic sites, a rational means of modulating edge reactivity remain to be developed. Here we demonstrate using first-principles calculations, X-ray absorption spectroscopy, as well as scanning transmission X-ray microscopy (STXM) imaging that edge corrugations yield distinctive spectroscopic signatures corresponding to increased localization of hybrid Mo 4d states. Independent spectroscopic signatures of such edge states are identified at both the S L2,3 and S K-edges with distinctive spatial localization of such states observed in S L2,3-edge STXM imaging. The presence of such low-energy hybrid states at the edge of the conduction band is seen to correlate with substantially enhanced electrocatalytic activity in terms of a lower Tafel slope and higher exchange current density. These results elucidate the nature of the edge electronic structure and provide a clear framework for its rational manipulation to enhance catalytic activity. PMID:29721532

Comparison of the elastic and inelastic scattering between 152Sm + 12C and 148Nd + 16O

International Nuclear Information System (INIS)

Zhao Kui; Lu Xiuqin; Cheng Yehao; Li Qingli; Li Min; Li Zhichang; Guo Jiyu; Li Shuyuan; Zhang Qinghua; Song Xiaobin; Jiang Chenglie

1994-01-01

Angular distributions of elastic and inelastic scattering have been measured for 152 Sm+ 12 C at 63.2 MeV and 148 Nd+ 16 O at 90.9 MeV. An evident interference pattern in the inelastic scattering has been observed for the first time in a strong Coulomb coupling system. (orig.)

An octanuclear molybdenum(VI) complex containing coordinatively bound 4,4'-di-tert-butyl-2,2'-bipyridine, [Mo8O22(OH)4(di-tBu-bipy)4]: synthesis, structure, and catalytic epoxidation of bio-derived olefins.

Science.gov (United States)

Amarante, Tatiana R; Neves, Patrícia; Tomé, Cátia; Abrantes, Marta; Valente, Anabela A; Paz, Filipe A Almeida; Pillinger, Martyn; Gonçalves, Isabel S

2012-03-19

The reaction of [MoO(2)Cl(2)(di-tBu-bipy)] (1) (di-tBu-bipy = 4,4'-di-tert-butyl-2,2'-bipyridine) with water at 100-120 °C in a Teflon-lined stainless steel autoclave, in an open reflux system, or in a microwave synthesis system gave the octanuclear complex [Mo(8)O(22)(OH)(4)(di-tBu-bipy)(4)] (2) as a microcrystalline powder in good yields. Single crystals of 2 suitable for X-ray diffraction were obtained by the reaction of MoO(3) and di-tBu-bipy in water at 160 °C for 3 days. The molecular structure of 2 comprises a purely inorganic core, Mo(4)O(8)(μ(3)-OH)(2)(μ(2)-O)(2), attached to two peripheral oxo-bridged binuclear units, Mo(2)O(4)(μ(2)-O)(2)(OH)(di-tBu-bipy)(2). The inorganic core is composed of a unique assembly of four {MoO(5)} distorted square pyramids connected to each other via edge-sharing. Overall, the octanuclear complex adopts a highly distorted form strongly resembling an "S"-shaped molecular unit. Complex 2 was applied in the catalytic epoxidation of the biorenewable olefins DL-limonene (Lim) and methyl oleate (Ole), using tert-butylhydroperoxide (TBHP) as an oxygen donor, under mild reaction conditions (55 °C, air). The reactions of Lim and Ole gave the respective epoxide monomers in fairly high selectivities at high conversions (89% 1,2-epoxy-p-menth-8-ene selectivity at 96% Lim conversion; 99% methyl 9,10-epoxystearate selectivity at 94% Ole conversion, reached within 24 h reaction). Iodometric titrations revealed no measurable "non-productive" decomposition of TBHP. © 2012 American Chemical Society

Catalytic conversion of CO, NO and SO2 on supported sulfide catalysts. Part 2. Catalytic reduction of NO and SO2 by CO

International Nuclear Information System (INIS)

Zhuang, S.-X.; Yamazaki, M.; Omata, K.; Takahashi, Y.; Yamada, M.

2001-01-01

To investigate the possibility of simultaneous catalytic reduction of NO and SO 2 by CO, reactions of NO, NO-CO, and NO-SO 2 -CO were performed on γ-alumina-supported sulfides of transition metals including Co, Mo, CoMo and FeMo. NO was decomposed into N 2 O and N 2 accompanied with the formation of SO 2 ; this serious oxidation of lattice sulfur resulted in the deactivation of the catalysts. The addition of CO to the NO stream suppressed SO 2 formation and yielded COS instead. A stoichiometric conversion of NO and CO to N 2 and CO 2 was observed above 350C on the CoMo and the FeMo catalysts. Although the CO addition lengthened catalyst life, it was not enough to maintain activity. After the NO-CO reaction, an XPS analysis showed the growth of Mo 6+ and SO 4 2- peaks, especially for the sulfided FeMo/Al 2 O 3 ; the FeMo catalyst underwent strong oxidation in the NO-CO reaction. The NO and the NO-CO reactions proceeded non-catalytically, consuming catalyst lattice sulfur to yield SO 2 or COS. The addition of SO 2 in the NO-CO system enabled in situ regeneration of the catalysts; the catalysts oxidized through abstraction of lattice sulfur experienced anew reduction and sulfurization through the SO 2 -CO reaction at higher temperature. NO and SO 2 were completely and catalytically converted at 400C on the sulfided CoMo/Al 2 O 3 . By contrast, the sulfided FeMo/Al 2 O 3 was easily oxidized by NO and hardly re-sulfided under the test conditions. Oxidation states of the metals before and after the reactions were determined. Silica and titania-supported CoMo catalysts were also evaluated to study support effects

Vertical MoSe2-MoO x p-n heterojunction and its application in optoelectronics

Science.gov (United States)

Chen, Xiaoshuang; Liu, Guangbo; Hu, Yunxia; Cao, Wenwu; Hu, PingAn; Hu, Wenping

2018-01-01

The hybrid n-type 2D transition-metal dichalcogenide (TMD)/p-type oxide van der Waals (vdW) heterojunction nanosheets consist of 2D layered MoSe2 (the n-type 2D material) and MoO x (the p-type oxide) which are grown on SiO2/Si substrates for the first time via chemical vapor deposition technique, displaying the regular hexagon structures with the average length dimension of sides of ˜8 μm. Vertical MoSe2-MoO x p-n heterojunctions demonstrate obviously current-rectifying characteristic, and it can be tuned via gate voltage. What is more, the photodetector based on vertical MoSe2-MoO x heterojunctions displays optimal photoresponse behavior, generating the responsivity, detectivity, and external quantum efficiency to 3.4 A W-1, 0.85 × 108 Jones, and 1665.6%, respectively, at V ds = 5 V with the light wavelength of 254 nm under 0.29 mW cm-2. These results furnish a building block on investigating the flexible and transparent properties of vdW and further optimizing the structure of the devices for better optoelectronic and electronic performance.

Study of the effect of different mixed supports on the catalytic activity and the structure of Bi{sub 2}Mo{sub x}W{sub 1-x}O{sub 6} catalysts; Estudio del efecto de diferentes soportes mixtos en la actividad catalitica y las caracteristicas estructurales de catalizadores de Bi{sub 2}Mo{sub x}W{sub 1-x}O{sub 6}

Energy Technology Data Exchange (ETDEWEB)

Rangel, R.; Cervantes L, J. L.; Espino, J. [Universidad Michoacana de San Nicolas de Hidalgo, Facultad de Ingenieria Quimica, Division de Estudios de Posgrado, 58060 Morelia, Michoacan (Mexico); Nunez G, R. [IPN, Centro de Investigacion y de Estudios Avanzados, Unidad Merida, Departamento de Fisica Aplicada, 97310 Merida, Yucatan (Mexico); Bartolo P, P. [Universidad de Sonora, Departamento de Matematicas, 83000 Hermosillo, Sonora (Mexico); Gomez C, A.; Diaz, G., E-mail: rrangel@umich.mx [UNAM, Instituto de Fisica, 04510 Mexico D. F. (Mexico)

2014-07-01

A series of Bi{sub 2}Mo{sub x}W{sub 1-x}O{sub 6} catalysts supported on Al{sub 2}O{sub 3}-SiO{sub 2}, SiO{sub 2}-TiO{sub 2} and activated carbon were synthesized. The aim was to compare the different supports and calcination temperature of catalysts, studying their efficiency and activation temperature in the CO oxidation reaction. The catalysts active phase, Bi{sub 2}Mo{sub x}W{sub 1-x}O{sub 6} was made by means of chemical precipitation procedure starting from high purity (NH{sub 4}){sub 6}Mo{sub 7}O{sub 24}·4H{sub 2}O, (NH{sub 4}){sub 6}W{sub 12}O{sub 6}·H{sub 2}O, Bi(NO{sub 3}){sub 2}·5H{sub 2}O compounds, which afterwards, were supported on Al{sub 2}O{sub 3}-SiO{sub 2}, SiO{sub 2}-TiO{sub 2} and activated carbon through impregnation. The catalysts characterization was carried out by means of X-ray diffraction analysis, scanning electron microscopy and surface area determination (Bet method). Regarding the catalytic activity the Bi{sub 2}Mo{sub x}W{sub 1-x}O{sub 6}/carbon activated compound synthesized at 500 grades C was the best catalyst being activated at 125 grades C reaching 90% conversion. It is concludes that was observed an effect of calcination temperature and the support on the different values reached for the catalytic activity. (Author)

Mo-V-Te-Nb oxides as catalysts for ethene production by oxidative dehydrogenation of ethane

Energy Technology Data Exchange (ETDEWEB)

Hartmann, D. [Technische Universitaet Muenchen, Garching (Germany). Dept. of Chemistry and Catalysis Research Center; Meiswinkel, A.; Thaller, C.; Bock, M.; Alvarado, L. [Linde AG, Pullach (Germany)

2013-11-01

The availability of ethane in shale gas, as well as the interest in valorising previously underutilized carbon feedstocks, makes the oxidative dehydrogenation (ODH) of ethane an attractive alternative to the industrially established processes for production of ethylene. Mo-V-Te-Nb mixed oxide has been chosen as catalyst for the ODH reaction in view of its outstanding ability to activate alkane molecules. Catalytic test results showed that this type of catalyst can selectively oxidize ethane to ethene at moderate temperatures (350-400 C) with minor production of CO{sub x}. The catalytic performance of Mo-V-Te-Nb mixed-oxide is mainly attributable to the crystalline phase 'M1'. Rietveld analysis of the X-Ray diffractograms allowed us to quantify the amount of MoVTeNb oxide that has crystallized as M1. In this way, it was possible to find a linear correlation of the reaction rate with the abundance of M1 in the solid. Therefore, it is clear that for improving the efficiency of MoVTeNb oxide in ODH, the amount of M1 in the catalyst should be maximized. With this purpose, several MoVTeNb oxides were subject to different thermal treatments prior to the catalytic test. Structural changes in the catalyst were monitored by in-situ XRD technique. Under oxidative atmosphere, it was observed a recrystallization of M2 and possibly, amorphous oxide, into M1 phase, leading to correspondingly more active and selective catalysts (selectivities above 95 % for ethane conversions up to 40 % under industrially relevant conditions). The active site of M1 involves V species, likely with redox properties enhanced by the proximity of Mo and Te species, while the function of the crystalline structure itself is to provide the spatial configuration that allows interaction between these species. However, ethene formation rate was observed to be independent of the V content of the samples. The vanadium species exposed at the surface were studied by LEIS and by IR spectroscopy of CO

Electric conductivity and lattice disorder of PbMoO4 crystals

International Nuclear Information System (INIS)

Bollmann, W.

1980-01-01

From differential thermal analysis (DTA), thermal etching, perfectly reversable redox treatments and electric conductivity it is concluded that the Pb/Mo ratio of the PbMoO 4 crystals is always 1 and that phase transitions do not occur. Pb 3+ ions detectable by an absorption band at 435 nm cause a p-conductivity due to the reaction Pb 3+ reversible Pb ++ + e + . At elevated temperatures the p-conductivity increases with increasing oxygen partial pressure of the surrouding atmosphere. The influence of foreign ions on the concentration of ionic and electronic defects in PbMoO 4 , CaMoO 4 , PbO, and PbTiO 3 can be explained by an anti-Frenkel disorder of the oxygen ion sublattice. For PbMoO 4 crystals the mobility O -- ion vacancies and the free formation enthalpy of anti-Frenkel defects are found to be vsub(v) = 9160/T exp (-1.15 eV/kT) cm 2 K/Vs and gsub(AF) = 3.6 kT - 2.2 eV, respectively. (author)

First-Principles Study of MoO3/Graphene Composite as Cathode Material for High-Performance Lithium-Ion Batteries

Science.gov (United States)

Cui, Yanhua; Zhao, Yu; Chen, Hong; Wei, Kaiyuan; Ni, Shuang; Cui, Yixiu; Shi, Siqi

2018-03-01

Using first-principles calculations, we have systematically investigated the adsorption and diffusion behavior of Li in MoO3 bulk, on MoO3 (010) surface and in MoO3/graphene composite. Our results indicate that, in case of MoO3 bulk, Li diffusion barriers in the interlayer and intralayer spaces are 0.55 eV and 0.58 eV respectively, which are too high to warrant fast Lithium-ion charge/discharge processes. While on MoO3 (010) surface, Li exhibits a diffusion barrier as low as 0.07 eV which guarantees an extremely fast Li diffusion rate during charge/discharge cycling. However, in MoO3/graphene monolayer, Li diffusion barrier is at the same level as that on MoO3 (010) surface, which also ensures a very rapid Li charge/discharge rate. The rapid Li charge/discharge rate in this system originates from the removal of the upper dangling O1 atoms which hinder the Li diffusion on the lower MoO3 layer. Besides this, due to the interaction between Li and graphene, the Li average binding energy increases to 0.14 eV compared to its value on MoO3 (010) surface which contributes to a higher voltage. Additionally, the increased ratio of surface area provides more space for Li storage and the capacity of MoO3/graphene composite increases up to 279.2 mAhg-1. The last but not the least, due to the high conductivity of graphene, the conductivity of MoO3/graphene composite enhances greatly which is beneficial for electrode materials. In the light of present results, MoO3/graphene composite exhibits higher voltage, good conductivity, large Li capacity and very rapid Li charge/discharge rate, which prove it as a promising cathode material for high-performance lithium-ion batteries (LIBs).

Promoted V2O5/TiO2 catalysts for selective catalytic reduction of NO with NH3 at low temperatures

DEFF Research Database (Denmark)

Putluru, Siva Sankar Reddy; Schill, Leonhard; Godiksen, Anita

2016-01-01

characterized by N2 physisorption, XRPD, NH3-TPD, H2-TPR, Raman, FTIR and EPR spectroscopy to investigate the properties of the catalysts. XRPD, Raman and FTIR showed that promotion with 15 wt.% HPA does not cause V2O5 to be present in crystalline form, also at a loading of 5 wt.% V2O5. Hence, use of HPAs does......The influence of varying the V2O5 content (3–6 wt.%) was studied for the selective catalytic reduction (SCR) of nitrogen oxides by ammonia on heteropoly acid (HPA)- and tungsten oxide (WO3)-promoted V2O5/TiO2 catalysts. The SCR activity and alkali deactivation resistance of HPA-promoted V2O5/TiO2...... catalysts was found to be much higher than for WO3-promoted catalysts. By increasing the vanadium content from 3 to 5 wt.% the catalysts displayed a two fold increase in activity at 225 °C and retained their initial activity after alkali doping at a molar K/V ratio of 0.181. Furthermore, the catalysts were...

Ionic Liquid-Assisted Synthesis of Nanoscale (MoS2)x(SnO2)1-x on Reduced Graphene Oxide for the Electrocatalytic Hydrogen Evolution Reaction.

Science.gov (United States)

Ravula, Sudhir; Zhang, Chi; Essner, Jeremy B; Robertson, J David; Lin, Jian; Baker, Gary A

2017-03-08

Layered transition metal dichalcogenides (TMDs) have attracted increased attention due to their enhanced hydrogen evolution reaction (HER) performance. More specifically, ternary TMD nanohybrids, such as MoS 2(1-x) Se 2x or bimetallic sulfides, have arisen as promising electrocatalysts compared to MoS 2 and MoSe 2 due to their electronic, morphologic, and size tunabilities. Herein, we report the successful synthesis of few-layered MoS 2 /rGO, SnS 2 /rGO, and (MoS 2 ) x (SnO 2 ) 1-x /rGO nanohybrids anchored on reduced graphene oxide (rGO) through a facile hydrothermal reaction in the presence of ionic liquids as stabilizing, delayering agents. Spectroscopic and microscopic techniques (electron microscopy, X-ray diffraction, Raman spectroscopy, neutron activation analysis, and UV-vis spectrophotometry) are used to validate the hierarchical properties, phase identity, and the smooth compositional tunability of the (MoS 2 ) x (SnO 2 ) 1-x /rGO nanohybrids. Linear sweep voltammetry measurements reveal that incorporation of Sn into the ternary nanohybrids (as a discrete SnO 2 phase) greatly reduces the overpotential by 90-130 mV relative to the MoS 2 electrocatalyst. Significantly, the (MoS 2 ) 0.6 (SnO 2 ) 0.4 /rGO nanohybrid displays superior catalytic performance over MoS 2 alone, exhibiting a low overpotential (η 10 ) of 263 ± 5 mV and a small Tafel slope of 50.8 mV dec -1 . The hybrid catalyst shows high stability for the HER in acidic solutions, with negligible activity loss after 1000 cycles. The hierarchical structures and large surface areas possessing exposed, active edge sites make few-layered (MoS 2 ) x (SnO 2 ) 1-x /rGO nanohybrids promising nonprecious metal electrocatalysts for the HER.

Behaviour of Co-Mo-Al/sub 2/O/sub 3/ catalysts in the hydrogenation of phenols

Energy Technology Data Exchange (ETDEWEB)

Weigold, H.

1982-10-01

The activity of a number of ring alkyl-substituted phenols in the direct hydrodeoxygenation reaction (i.e. C-O bond scission without prior ring hydrogenation) in the presence of a commercial Co-Mo-Al/sub 2/O/sub 3/ catalyst has been investigated. The results indicate that the catalytically active site is stereochemically demanding. It is proposed that the phenol ring hydrogenation and the direct hydrodeoxygenation reaction proceed on the same catalytic site. The ease of the direct hydrodeoxygenation reaction is retarded mainly when transfer of the substrate hydroxyl group onto a co-ordinatively unsaturated metal site on the catalyst is inhibited. This occurs when the catalyst hydroxyl group receptor site is occupied by a co-ordinating ligand (poison) or when substituents on the substrate direct the phenolic hydroxyl group away from this metal site. The catalytic behaviour of Co-Mo-Al/sub 2/O/sub 3/ can be 'transformed' to resemble more closely that of Ni-Mo-Al/sub 2/O/sub 3/ (high reductive capacity) when the reaction medium contains both excess H/sub 2/S and a co-ordinating ligand. It is proposed that this 'transformed' species is of importance in hydrodenitrogenation reactions in an H/sub 2/S-rich environment.

Mass of the 158Sm

International Nuclear Information System (INIS)

Zhao Kui; Guo Jiyu; Lu Xiuqin; Cheng Yehao; Huang Xiaolin; Ma Yong; Li Shuyuan; Ruan Ming; Li Zhichang; Jiang Chenglie

1997-01-01

A preliminary result was reported for the experiment to determine the mass of the heavier neutron-rich nucleus 158 Sm using the 160 Gd( 18 O, 20 Ne) two proton transfer reaction in last progress report. The average Q-value of (4.046 +- 0.102) MeV for the 160 Gd( 18 O, 20 Ne) 158 Sm reaction is given. A mass excess for 158 Sm of (-65.738 +- 0.102) MeV was derived. This is the first experimentally measured value of the mass of 158 Sm which is about 450 keV higher than the evaluation value from systematic trends listed in the 1993 atomic mass table. The new prediction shows better agreement with the measured values and a significant improvement over the earlier FRDM (finite-range droplet model) value

ITO-free flexible organic photovoltaics with multilayer MoO3/LiF/MoO3/Ag/MoO3 as the transparent electrode

International Nuclear Information System (INIS)

Chen, Shilin; Dai, Yunjie; Zhang, Hongmei; Zhao, Dewei

2016-01-01

We present efficient flexible organic photovoltaics (OPVs) with multiple layers of molybdenum oxide (MoO 3 )/LiF/MoO 3 /Ag/MoO 3 as the transparent electrode, where the thin Ag layer yields high conductivity and the dielectric layer MoO 3 /LiF/MoO 3 has high transparency due to optical interference, leading to improved power conversion efficiency compared with indium tin oxide (ITO) based devices. The MoO 3 contacting organic active layer is used as a buffer layer for good hole extraction. Thus, the multilayer MoO 3 /LiF/MoO 3 /Ag/MoO 3 can improve light transmittance and also facilitate charge carrier extraction. Such an electrode shows excellent mechanical bendability with a 9% reduction of efficiency after 1000 cycles of bending due to the ductile nature of the thin metal layer and dielectric layer used. Our results suggest that the MoO 3 /LiF/MoO 3 /Ag/MoO 3 multilayer electrode is a promising alternative to ITO as an electrode in OPVs. (paper)

Phase equilibria in the BaUO3-BaZrO3-BaMoO3 system

International Nuclear Information System (INIS)

Kurosaki, Ken; Yamanaka, Shinsuke; Matsuda, Tetsushi; Uno, Masayoshi; Yamamoto, Kazuya; Namekawa, Takashi

2002-01-01

The phase equilibria in the pseudo-ternary BaUO 3 -BaZrO 3 -BaMoO 3 system were studied to understand the thermochemical properties of the perovskite type gray oxide phase in high burnup MOX fuel. Thermodynamic equilibrium calculation for the system was performed by using a Chem Sage program under the various oxygen potentials. Solid solutions existing in the system were treated by an ideal solution model. The present calculation results well agreed with the previous reported post irradiation examination results, showing that BaMoO 3 was scarcely included in the gray oxide phase. (author)

Effects of the defects on the structural, electronic and magnetic properties of Sr{sub 2}FeMoO{sub 6}

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yan, E-mail: yan.zhang@chd.edu.cn [School of Materials Science and Engineering, Chang' an University, Xi' an 710061, Shaanxi (China); Ji, Vincent [ICMMO/SP2M, UMR CNRS 8182, Université Paris-Sud, 91405 Orsay Cédex (France); Xu, Ke-Wei [State Key Laboratory for Mechanical Behavior of Materials, Xi' an Jiaotong University, Xi' an 710049, Shaanxi (China)

2015-11-05

From the point of view of the half-metallic character and magnetization reduction, the structural, electronic and magnetic properties of the imperfect Sr{sub 2}FeMoO{sub 6} compound containing seven different defects of the Fe{sub Mo} or Mo{sub Fe} antisites, Fe–Mo interchange, V{sub Fe}, V{sub Mo}, V{sub O} or V{sub Sr} vacancies have been studied by using first-principles projector augmented wave (PAW) within generalized gradient approximation (GGA) as well as taking into account on-site Coulomb repulsive interaction (GGA + U). No obvious structural changes are observed for the imperfect Sr{sub 2}FeMoO{sub 6} compound containing Fe{sub Mo} or Mo{sub Fe} antisites, Fe–Mo interchange or V{sub Sr} vacancy defects. However, the six (eight) nearest oxygen neighbors of the vacancy move away from (close to) V{sub Fe} or V{sub Mo} (V{sub O}) vacancies. The half-metallic character is maintained for the imperfect Sr{sub 2}FeMoO{sub 6} compound containing Fe{sub Mo} antisite, V{sub Fe}, V{sub O} or V{sub Sr} vacancies, while it vanishes when Mo{sub Fe} antisite, Fe–Mo interchange or V{sub Mo} vacancy are presented. So the Mo{sub Fe} antisite, Fe–Mo interchange or V{sub Mo} vacancy defects have to be avoided in order to preserve the half-metallic character of the Sr{sub 2}FeMoO{sub 6} compound and thus usable in spintronics devices. In Fe{sub Mo} or Mo{sub Fe} antisites, Fe–Mo interchange cases, the spin moments of Fe (Mo) cations situated on Mo (Fe) antisites are in an antiferromagnetic coupling with those of Fe (Mo) cations on the regular sites. In V{sub Fe}, V{sub Mo}, V{sub O} or V{sub Sr} vacancies cases, a ferromagnetic coupling is obtained within each cation sublattice, while two cation sublattices are coupled antiferromagnetically. The total magnetic moments μ{sub tot} (μ{sub B}/f.u.) of the imperfect Sr{sub 2}FeMoO{sub 6} compound containing seven different defects decrease in the sequence of V{sub Sr} vacancy (4.38), V{sub Mo} vacancy (3.92), V{sub O

The lanthanoid(III) chloride oxoselenates(IV) MCl[SeO3] (M = Sm - Lu) with HoCl[TeO3]- or B-type structure

International Nuclear Information System (INIS)

Lipp, C.; Schleid, T.

2008-01-01

The B-type lanthanoid(III) chloride oxoselenates(IV) MCl[SeO 3 ] (M = Sm - Lu) crystallize in the orthorhombic space group Pnma (no. 62) with Z = 4 in the structure type of HoCl[TeO 3 ]. Their lattice constants are decreasing following the lanthanoid contraction from a = 730.01(7), b = 707.90(7), c 895.64(9) pm for SmCl[SeO 3 ] to a = 714.63(7), b = 681.76(7), c = 864.05(9) pm for LuCl[SeO 3 ]. In contrast to NdCl[SeO 3 ], the only representative of the A-type structure, where the coordination numbers of the Nd 3+ cations are 7+2 and 8, the B-type structure is dominated by pentagonal bipyramids [MO 5 Cl 2 ] 9- (CN(M 3+ ) = 7), which are connected via trans-oriented O..O edges to ∞ 1 {[MO 4/2 e O 1/1 t Cl 2/1 t ] 5- } chains (e = edge-sharing, t = terminal) running parallel to the [010] direction. Their inclination relative to each other allows for an alternating interconnection of these chains via Cl - and ψ 1 -tetrahedral [SeO 3 ] 2- anions to form a three-dimensional structure. The distances within the [SeO 3 ] 2- groups are in the normal range (d(Se-O) = 165 - 172 pm), while those of the O 2- and Cl - anions to the central M 3+ cation diminish in dependence of the increasing atomic number (d(M-O) = 226 - 244 pm / 216 - 232 pm, d(M-Cl) 277 - 278 pm / 266 - 270 pm, M = Sm / Lu). For the synthesis of the chloride oxoselenates(IV) MCl[SeO 3 ] the respective lanthanoid sesquioxide (M 2 O 3 ) and selenium dioxide (SeO 2 ) were reacted with either an eutectic mixture of RbCl and LiCl or with the corresponding lanthanoid trichloride (MCl 3 ) in evacuated silica ampoules for either five weeks at 500 C or one week at 850 C. (orig.)

Heterogeneous-catalytic redox reactions in nitrate - formate systems

International Nuclear Information System (INIS)

Ananiev, A.V.; Shilov, V.P.; Tananaev, I.G.; Brossard, Ph.; Broudic, J.Ch.

2000-01-01

It was found that an intensive destruction of various organic and mineral substances - usual components of aqueous waste solutions (oxalic acid, complexones, urea, hydrazine, ammonium nitrate, etc.) takes place under the conditions of catalytic denitration. Kinetics and mechanisms of urea and ammonium nitrate decomposition in the system HNO 3 - HCOOH - Pt/SiO 2 are comprehensively investigated. The behaviour of uranium, neptunium and plutonium under the conditions of catalytic denitration is studied. It is shown, that under the certain conditions the formic acid is an effective reducer of the uranium (VI), neptunium (VI, V) and plutonium (VI, IV) ions. Kinetics of heterogeneous-catalytic red-ox reactions of uranium (VI), neptunium (VI, V) and plutonium (VI, IV) with formic acid are investigated. The mechanisms of the appropriate reactions are evaluated. (authors)

A Structural Study on the Foaming Behavior of CaO-SiO2-MO (MO = MgO, FeO, or Al2O3) Ternary Slag System

Science.gov (United States)

Park, Youngjoo; Min, Dong Joon

2017-12-01

The foaming index of the CaO-SiO2-MO (MO = MgO, FeO, or Al2O3) ternary slag system with a fixed CaO/SiO2 ratio is measured to understand the effect of the ionic structure. At 1773 K (1500 °C), the foaming index of the slag increases with Al2O3 addition and decreases with MgO or FeO addition at a fixed CaO/SiO2 ratio. It is verified that the previous correlation between the foaming index and the physical properties could also be valid for the CaO-SiO2-(MgO or Al2O3) system. Raman spectroscopy for the CaO/SiO2 = 1.0 slag is applied to explain the foaming behavior from an ionic structural perspective. From the ionic structural viewpoint, the fractional change in each silicate anion unit is identified by de-convoluted Raman spectra. The Raman spectra indicate that the silicate network structure is polymerized with Al2O3 as an aluminosilicate structure; in contrast, de-polymerization occurs by MgO or FeO addition. Furthermore, the relationship between the silicate structure and the thermodynamic stability function is discussed. Since the ionic structure of the molten slag affects various physical/thermodynamic properties, the foaming behavior could be successfully interpreted from the ionic structural viewpoint.

Thermal and x-ray studies on Tl2U(MoO4)3 and Tl4U(MoO4)4

International Nuclear Information System (INIS)

Dahale, N.D.; Keskar, Meera; Kulkarni, N.K.; Singh Mudher, K.D.

2006-01-01

In the quaternary Tl-U(IV)-Mo-O system, two new compounds namely Tl 2 U(MoO 4 ) 3 and Tl 4 U(MoO 4 ) 4 were prepared and characterized by powder X-ray diffraction and thermal methods. These compounds were prepared by solid state reactions of Tl 2 MoO 4 , UMoO 5 and MoO 3 in the required stoichiometric ratio at 500 deg C in evacuated sealed quartz ampoule. The XRD data of Tl 2 U(MoO 4 ) 3 and Tl 4 U(MoO 4 ) 4 were indexed on orthorhombic cell. TG curves of Tl 2 U(MoO 4 ) 3 and Tl 4 U(MoO 4 ) 4 did not show any weight change up to 700 deg C in an inert atmosphere. During heating in an inert atmosphere, Tl 2 U(MoO 4 ) 3 and Tl 4 U(MoO 4 ) 4 showed endothermic Dta peaks due to melting of the compounds at 519 and 565 deg C, respectively. (author)

Mn-Ce-V-WOx/TiO2 SCR Catalysts: Catalytic Activity, Stability and Interaction among Catalytic Oxides

Directory of Open Access Journals (Sweden)

Xuteng Zhao

2018-02-01

Full Text Available A series of Mn-Ce-V-WOx/TiO2 composite oxide catalysts with different molar ratios (active components/TiO2 = 0.1, 0.2, 0.3, 0.6 have been prepared by wet impregnation method and tested in selective catalytic reduction (SCR of NO by NH3 in a wide temperature range. These catalysts were also characterized by X-ray diffraction (XRD, Transmission Electron Microscope (TEM, in situ Fourier Transform infrared spectroscopy (in situ FTIR, H2-Temperature programmed reduction (H2-TPR and X-ray photoelectron spectroscopy (XPS. The results show the catalyst with a molar ratio of active components/TiO2 = 0.2 exhibits highest NO conversion value between 150 °C to 400 °C and good resistance to H2O and SO2 at 250 °C with a gas hourly space velocity (GHSV value of 40,000 h−1. Different oxides are well dispersed and interact with each other. NH3 and NO are strongly adsorbed on the catalyst surface and the adsorption of the reactant gas leads to a redox cycle with the valence state change among the surface oxides. The adsorption of SO2 on Mn4+ and Ce4+ results in good H2O and SO2 resistance of the catalyst, but the effect of Mn and Ce are more than superior water and sulfur resistance. The diversity of valence states of the four active components and their high oxidation-reduction performance are the main reasons for the high NO conversion in this system.

Three-Dimensional Heterostructures of MoS 2 Nanosheets on Conducting MoO 2 as an Efficient Electrocatalyst To Enhance Hydrogen Evolution Reaction

KAUST Repository

Nikam, Revannath Dnyandeo

2015-10-05

Molybdenum disulfide (MoS) is a promising catalyst for hydrogen evolution reaction (HER) because of its unique nature to supply active sites in the reaction. However, the low density of active sites and their poor electrical conductivity have limited the performance of MoS in HER. In this work, we synthesized MoS nanosheets on three-dimensional (3D) conductive MoO via a two-step chemical vapor deposition (CVD) reaction. The 3D MoO structure can create structural disorders in MoS nanosheets (referred to as 3D MoS/MoO), which are responsible for providing the superior HER activity by exposing tremendous active sites of terminal disulfur of S2 (in MoS) as well as the backbone conductive oxide layer (of MoO) to facilitate an interfacial charge transport for the proton reduction. In addition, the MoS nanosheets could protect the inner MoO core from the acidic electrolyte in the HER. The high activity of the as-synthesized 3D MoS/MoO hybrid material in HER is attributed to the small onset overpotential of 142 mV, a largest cathodic current density of 85 mA cm, a low Tafel slope of 35.6 mV dec, and robust electrochemical durability.

Three-Dimensional Heterostructures of MoS 2 Nanosheets on Conducting MoO 2 as an Efficient Electrocatalyst To Enhance Hydrogen Evolution Reaction

KAUST Repository

Nikam, Revannath Dnyandeo; Lu, Ang-Yu; Sonawane, Poonam Ashok; Kumar, U. Rajesh; Yadav, Kanchan; Li, Lain-Jong; Chen, Yit Tsong

2015-01-01

Molybdenum disulfide (MoS) is a promising catalyst for hydrogen evolution reaction (HER) because of its unique nature to supply active sites in the reaction. However, the low density of active sites and their poor electrical conductivity have limited the performance of MoS in HER. In this work, we synthesized MoS nanosheets on three-dimensional (3D) conductive MoO via a two-step chemical vapor deposition (CVD) reaction. The 3D MoO structure can create structural disorders in MoS nanosheets (referred to as 3D MoS/MoO), which are responsible for providing the superior HER activity by exposing tremendous active sites of terminal disulfur of S2 (in MoS) as well as the backbone conductive oxide layer (of MoO) to facilitate an interfacial charge transport for the proton reduction. In addition, the MoS nanosheets could protect the inner MoO core from the acidic electrolyte in the HER. The high activity of the as-synthesized 3D MoS/MoO hybrid material in HER is attributed to the small onset overpotential of 142 mV, a largest cathodic current density of 85 mA cm, a low Tafel slope of 35.6 mV dec, and robust electrochemical durability.

MoS{sub 2} on an amorphous HfO{sub 2} surface: An ab initio investigation

Energy Technology Data Exchange (ETDEWEB)

Scopel, W. L., E-mail: wlscopel@if.uff.br [Departamento de Física, Universidade Federal do Espírito Santo, Vitória, Brazil and Departamento de Ciências Exatas, Universidade Federal Fluminense, Volta Redonda, Rio de Janerio (Brazil); Miwa, R. H., E-mail: hiroki@infis.ufu.br; Schmidt, T. M., E-mail: tome@infis.ufu.br [Instituto de Física, Universidade Federal de Uberlândia, Uberlândia, Minas Gerais (Brazil); Venezuela, P., E-mail: vene@if.uff.br [Instituto de Física, Universidade Federal Fluminense, Niterói, Rio de Janerio (Brazil)

2015-05-21

The energetic stability, electronic and structural properties of MoS{sub 2} adsorbed on an amorphous a-HfO{sub 2} surface (MoS{sub 2}/HfO{sub 2}) are examined through ab initio theoretical investigations. Our total energy results indicate that the formation of MoS{sub 2}/HfO{sub 2} is an exothermic process with an adsorption energy of 34 meV/Å{sup 2}, which means that it is more stable than similar systems like graphene/HfO{sub 2} and MoS{sub 2}/SiO{sub 2}. There are no chemical bonds at the MoS{sub 2}-HfO{sub 2} interface. Upon formation of MoS{sub 2}/HfO{sub 2}, the electronic charge distribution is mostly localized at the interface region with no net charge transfer between the adsorbed MoS{sub 2} sheet and –HfO{sub 2} surface. However, the MoS{sub 2} sheet becomes n-type doped when there are oxygen vacancies in the HfO{sub 2} surface. Further investigation of the electronic distribution reveals that there are no electron- and hole-rich regions (electron-hole puddles) on the MoS{sub 2} sheet, which makes this system promising for use in high-speed nanoelectronic devices.

Effects of γ-irradiation and ageing on surface and catalytic properties of nano-sized Cu O/Mg O system

International Nuclear Information System (INIS)

El-Molla, S. A.; Ismail, S. A.; Ibrahim, M. M.

2011-01-01

0.2 Cu O/Mg O system prepared by impregnation method was calcined at 350 and 450 C. The effects of γ-rays (0.2-1.6 MGy) on its structure, surface and catalytic properties were investigated by using XRD, N 2 -adsorption at -196 C and catalytic conversion of isopropanol at 150-275 C using a flow technique. The results revealed that the investigated solids consisted of nano-sized Mg O as a major phase besides Cu O and trace amount of Cu 2 O. γ-Irradiation of the solids investigated exerted measurable changes in their surface and catalytic properties dependent on the calcination temperature and dose of irradiation. The catalysts investigated acted as active dehydrogenation solids. The five years-ageing of different solids showed limited changes of their surface and catalytic properties indicating a good catalytic stability of the irradiated prepared solids. (Author)

Effects of {gamma}-irradiation and ageing on surface and catalytic properties of nano-sized Cu O/Mg O system

Energy Technology Data Exchange (ETDEWEB)

El-Molla, S. A. [Ain Shams University, Faculty of Education, Chemistry Deparment, Roxy, Heliopolis, 11757 Cairo (Egypt); Ismail, S. A.; Ibrahim, M. M., E-mail: saharelmolla@yahoo.com [National Center for Radiation Research and Technology, Nasr City, P.O. Box 29, 11731 Cairo (Egypt)

2011-07-01

0.2 Cu O/Mg O system prepared by impregnation method was calcined at 350 and 450 C. The effects of {gamma}-rays (0.2-1.6 MGy) on its structure, surface and catalytic properties were investigated by using XRD, N{sub 2}-adsorption at -196 C and catalytic conversion of isopropanol at 150-275 C using a flow technique. The results revealed that the investigated solids consisted of nano-sized Mg O as a major phase besides Cu O and trace amount of Cu{sub 2}O. {gamma}-Irradiation of the solids investigated exerted measurable changes in their surface and catalytic properties dependent on the calcination temperature and dose of irradiation. The catalysts investigated acted as active dehydrogenation solids. The five years-ageing of different solids showed limited changes of their surface and catalytic properties indicating a good catalytic stability of the irradiated prepared solids. (Author)

Raman spectroscopic study of structure and crystallisation behaviour of MoO3-La2O3-B2O3 and MoO3-ZnO-B2O3 glasses

Science.gov (United States)

Aleksandrov, L.; Komatsu, T.; Nagamine, K.; Oishi, K.

2011-03-01

In this study, we focus on the structure and crystallization behavior of MoO3-La2O3-B2O3 and MoO3-ZnO-B2O3 glasses. Glasses of both systems were prepared by a melt-quenching method. The thermal stability of the glasses was examined using differential thermal anaysis (DTA) measurements, and the crystalline phases formed by heat treatments were identified by X-ray diffraction (XRD) analysis. Raman scattering spectra at room temperature for the glasses and crystallized samples were measured with a laser microscope operated with an Ar+ (wavelength: 488 nm) laser. DTA measurements indicated that the thermal stability against crystallization of the glasses decreases drastically with increasing MoO3 content. XRD analysis confirmed that crystallization at 600°C for 3 h of glass with the nominal composition of 50MoO3-25La2O3-25B2O3 resulted in the formation of monoclinic LaMoBO6. Crystallization of 50ZnO-xMoO3-(50-x)B2O3 glasses formed triclinic α-ZnMoO4 as an initial crystalline phase. Moreover, for 30 mol% MoO3 glass, transmission electron microscopy observations showed the formation of α-ZnMoO4 nanocrystals with a diameter of ~ 5 nm. Raman bands at 860, 930 and 950 cm-1 suggested that the coordination state of Mo6+ ions in the glasses were mainly (MoO4)2- tetrahedral units. Therefore, MoO3-containing glasses have good potential for optical applications.

Modification of TiO{sub 2} nanorods by Bi{sub 2}MoO{sub 6} nanoparticles for high performance visible-light photocatalysis

Energy Technology Data Exchange (ETDEWEB)

Li Na; Zhu Li [School of Chemistry and Chemical Engineering, South China University of Technology, 381 Wushan Road, Guangzhou 510640 (China); Zhang Weide, E-mail: zhangwd@scut.edu.cn [School of Chemistry and Chemical Engineering, South China University of Technology, 381 Wushan Road, Guangzhou 510640 (China); Yu Yuxiang; Zhang Wenhui; Hou Meifang [School of Chemistry and Chemical Engineering, South China University of Technology, 381 Wushan Road, Guangzhou 510640 (China)

2011-10-13

Highlights: > Bi{sub 2}MoO{sub 6}/TiO{sub 2} heterojunction photocatalysts. > Effective separation of photoexcited electrons and holes. > High visible light photocatalytic activity. - Abstract: In this work, TiO{sub 2} nanorods were prepared by a hydrothermal process and then Bi{sub 2}MoO{sub 6} nanoparticles were deposited onto the TiO{sub 2} nanorods by a solvothermal process. The nanostructured Bi{sub 2}MoO{sub 6}/TiO{sub 2} composites were extensively characterized by X-ray diffraction, scanning and transmission electron microscopy, X-ray photoelectron spectroscopy and UV-vis diffuse reflectance spectroscopy. The photocatalytic activity of the Bi{sub 2}MoO{sub 6}/TiO{sub 2} composites was evaluated by degradation of methylene blue. The Bi{sub 2}MoO{sub 6}/TiO{sub 2} composites exhibit higher catalytic activity than pure Bi{sub 2}MoO{sub 6} and TiO{sub 2} for degradation of methylene blue under visible light irradiation ({lambda} > 420 nm). Further investigation revealed that the ratio of Bi{sub 2}MoO{sub 6} to TiO{sub 2} in the composites greatly influenced their photocatalytic activity. The experimental results indicated that the composite with Bi{sub 2}MoO{sub 6}:TiO{sub 2} = 1:3 exhibited the highest photocatalytic activity. The enhancement mechanism of the composite catalysts was also discussed.

Surface electronic structure-catalytic activity correlation of partially reduced molybdenum oxide(s) for the isomerization of light alkenes and alkanes

International Nuclear Information System (INIS)

Al-Kandari, S; Al-Kandari, H; Al-Kharafi, F; Katrib, A

2008-01-01

Catalytic activity-surface electronic structure correlation was carried out using surface XPS-UPS techniques. In situ reduction by hydrogen, were carried out at similar experimental conditions to those employed for the catalytic reactions. In the case of MoO 3 deposited on TiO 2 , the reduction to MoO 2 state with the bifunctional MoO 2 (H x ) ac phase on its surface starts at 573 K and reaches a stable state at temperatures between 653-673 K. In the case of alumina support, a strong metal-support interaction takes place during the catalyst preparation, leading to Al 2 (MoO 4 ) 3 complex formation as characterized by XRD. The reduction process(s) of this complex by hydrogen as a function of temperature is different from what is observed in the case of titania support. The changes in the chemical structure of the sample surface in both systems were tested for the catalytic reactions of 1-pentene and n-pentane

Polarographic, spectrophotometric and coulometric studies of MoO=4 in H2SO4

International Nuclear Information System (INIS)

Tokoro, R.; Bertotti, M.

1990-01-01

This study characterizes the polarographic process of Mo O sup(=) sub(4) in H sub(2)SO sub(4) medium, determining which species is responsible by catalytic cycle. Spectrophotometric and coulometric studies are also described. (author)

Investigation of radiation shielding properties for MeO-PbCl2-TeO2 (MeO = Bi2O3, MoO3, Sb2O3, WO3, ZnO) glasses

Science.gov (United States)

Sayyed, M. I.; Çelikbilek Ersundu, M.; Ersundu, A. E.; Lakshminarayana, G.; Kostka, P.

2018-03-01

In this work, glasses in the MeO-PbCl2-TeO2 (MeO = Bi2O3, MoO3, Sb2O3, WO3, ZnO) system, which show a great potential for optoelectronic applications, were used to evaluate their resistance under high energy ionizing radiations. The basic shielding quantities for determining the penetration of radiation in glass, such as mass attenuation coefficient (μ/ρ), half value layer (HVL), mean free path (MFP) and exposure buildup factor (EBF) values were investigated within the energy range 0.015 MeV ‒ 15 MeV using XCOM program and variation of shielding parameters were compared with different glass systems and ordinary concrete. From the derived results, it was determined that MeO-PbCl2-TeO2 (MeO = Bi2O3, MoO3, Sb2O3, WO3, ZnO) glasses show great potentiality to be used under high energy radiations. Among the studied glass compositions, Bi2O3 and WO3 containing glasses were found to possess superior gamma-ray shielding effectiveness.

Optical spectroscopy of Sm(3+) doped Na2O-ZnO-La2O3-TeO2 glasses.

Science.gov (United States)

Sobczyk, Marcin

2015-10-05

Telluride glasses with the composition xSm2O3-(7-x)La2O3-3Na2O-25ZnO-65TeO2 (where x=0.1, 1, 2, 5 and 7 mol%) were obtained by the melt quenching technique. Electronic absorption and fluorescence spectra as well as fluorescence dynamics of the Sm(3+)-doped title glasses are presented and analysed in detail. A Judd-Ofelt intensity analysis of the absorption spectrum at 300 K has been applied for determination of Ωλ parameters (Ω2=3.10, Ω4=3.80, Ω6=1.61×10(-20) cm(2)) which in turn have been used for calculations of the radiative transition probabilities (AT), the natural (radiative) lifetimes (τR) of the (4)G5/2 level of Sm(3+), the fluorescence branching ratios (β) and the emission cross-sections (σem). The τR value of the (4)G5/2 level amount to 1546 μs and is slightly higher than the measured decay time of 1306 μs. With the increasing of Sm2O3 concentration from 0.1 to 7.0 mol% the experimental lifetime of the fluorescent level decreases from 1306 to 41 μs. An analysis of the non-radiative decay was based on the cross-relaxation mechanisms. The optical achieved results indicate that the investigated glasses are potentially applicable as an orange and/or red laser host. Copyright © 2015 Elsevier B.V. All rights reserved.

Fast synthesis of the polycrystalline materials on the base of Zn 3 V2 MoO11 and Zn 2.5 VMoO8

Directory of Open Access Journals (Sweden)

Maya Markova-Velichkova

2009-12-01

Full Text Available In our study we applied two different techniques for the preparation of Zn3V2MoO11 and Zn2.5VMoO8 polycrystalline materials - melt quenching method (up-bottom and mechanochemical synthesis (bottom- up. These compounds belong to the family of materials with general formula M2.5VMoO8 (M=Zn, Mg, Mn, Co. They are potential candidates as catalysts in processes of selective oxidation of hydrocarbons. Until now, these two compounds were obtained by conventional solid state reaction. Using infrared spectroscopy and X-ray diffraction we proved that the melt quenching technique is a quite appropriate method for the synthesis of bulk Zn3V2-MoO11 phase. Mechanochemical activation is more appropriated for the preparation of nonosized Zn2.5VMoO8 powder. It was established that the melt quenching technique and mechanochemical activation are faster in comparison with conventional ceramic methods for the given synthesis.

Systematic study on the influence of the morphology of α-MoO3 in the selective oxidation of propylene

DEFF Research Database (Denmark)

Schuh, Kirsten; Kleist, Wolfgang; Høj, Martin

2015-01-01

A variety of morphologically different α-MoO3 samples were prepared by hydrothermal synthesis and applied in the selective oxidation of propylene. Their catalytic performance was compared to α-MoO3 prepared by flame spray pyrolysis (FSP) and a classical synthesis route. Hydrothermal synthesis from...... with nitric acid at 180°C. Particularly, if nitric acid was used during synthesis, the rod-like morphology of the samples could be stabilized during calcination at 550°C and the following catalytic activity tests, which was beneficial for the catalytic performance in propylene oxidation. Characterization...... studies using X-ray diffraction (XRD), scanning electron microscopy (SEM) and Raman spectroscopy showed that those samples, which retained their rod-like morphology during the activity tests, yielded the highest propylene conversion....

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

Electrochemical, H2O2-Boosted Catalytic Oxidation System

Science.gov (United States)

Akse, James R.; Thompson, John O.; Schussel, Leonard J.

2004-01-01

An improved water-sterilizing aqueous-phase catalytic oxidation system (APCOS) is based partly on the electrochemical generation of hydrogen peroxide (H2O2). This H2O2-boosted system offers significant improvements over prior dissolved-oxygen water-sterilizing systems in the way in which it increases oxidation capabilities, supplies H2O2 when needed, reduces the total organic carbon (TOC) content of treated water to a low level, consumes less energy than prior systems do, reduces the risk of contamination, and costs less to operate. This system was developed as a variant of part of an improved waste-management subsystem of the life-support system of a spacecraft. Going beyond its original intended purpose, it offers the advantage of being able to produce H2O2 on demand for surface sterilization and/or decontamination: this is a major advantage inasmuch as the benign byproducts of this H2O2 system, unlike those of systems that utilize other chemical sterilants, place no additional burden of containment control on other spacecraft air- or water-reclamation systems.

Correlation Between Electrical Conductivity and Catalytic Property in 78V{sub 2}O{sub 5}–15P{sub 2}O{sub 5}–7B{sub 2}O{sub 3} Glass Containing Fe{sub 2}O{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Jeong, Hwa-Jin; Kim, Jong-hwan; Ryu, Bong-Ki [Pusan National University, Busan (Korea, Republic of)

2016-12-15

In this study, we established a correlation between the electrical conductivity and catalytic properties of vanadium borophosphate glass containing Fe{sub 2}O{sub 3}. Glasses were synthesized in the 78V{sub 2}O{sub 5}–15P{sub 2}O{sub 5}–7B{sub 2}O{sub 3} ternary-system containing x mol% Fe{sub 2}O{sub 3} (x = 1, 5, 7.5, and 10). Electrical conductivity was measured at 45 ℃ for samples heat-treated at 340 ℃ for 12 h. To examine catalytic effects, we used TGA measurements of a mixture of fatty acid and sample powders. Fourier transform infrared spectroscopy (FTIR) was used to analyze the structural changes after crystallization, while X-ray photoelectron spectroscopy (XPS) analysis indicated changes with different valence state ions. X-ray diffraction (XRD) analysis of the structure array verified these inferred changes. Conductivity and catalytic effects are discussed in relation to the migration of vanadate ions and iron ions with different valence states due to the increase crystallinity.

K0.78Na0.22MoO2AsO4

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Ahmed Driss

2013-08-01

Full Text Available The title compound, potassium sodium dioxidomolybdenum(VI arsenate, K0.78Na0.22MoO2AsO4, was synthesized by a solid-state reaction route. The structure is built up from corner-sharing MoO6 octahedra and AsO4 tetrahedra, creating infinite [MoAsO8]∞ chains running along the b-axis direction. As, Mo and all but one O atom are on special positions (4c with m symmetry and K (occupancy 0.78 is on a position (4a of -1 in the tunnels. The possible motion of the alkali cations has been investigated by means of the bond-valance sum (BVS model. The simulation shows that the Na+ motion appears to be easier mainly along the b-axis direction. Structural relationships between the different compounds of the AMoO2AsO4 (A = Ag, Li, Na, K, Rb series and MXO8 (M = V; X = P, As chains are discussed.

Multifunctional Sm2-xDyxZr2O7 pyrochlore system: potential ionic conductors and photocatalysts

International Nuclear Information System (INIS)

Grover, V.; Sayed, Farheen N.; Bhattacharyya, K.; Jain, D.; Pillai, C.G.S.; Tyagi, A.K.; Arya, A.

2010-01-01

Full text: Pyrochlores have garnered considerable interest over the years because of a range of potentially useful properties such as fast-ion (mainly anion) conductivity, electrical conductivity, catalysis, luminescence etc. In present work a series of Sm 2-x Dy x Zr 2 O 7 compounds (0.0 ≤ x ≤ 2.0) were synthesized by gel combustion and characterized by Powder XRD and Raman spectroscopic studies. XRD studies revealed the system to be single-phasic throughout with the retention of pyrochlore phase till 40 mol% of Dy 3+ beyond which, an order-disorder phase transition occurred resulting in a defect fluorite structure. Surprisingly, Raman studies showed the retention of pyrochlore type ordering till the other end member, i.e. Dy 2 Zr 2 O 7 . This is the first study, which reports the retention of a weak pyrochlore type superstructure in Dy 2 Zr 2 O 7 system. Ionic conductivity measurements were performed on these samples, which showed that the activation Energy (E a ) increases with increase in Dy 3+ mol% owing to the decreased mobility with increasing degree of disorder. The representative nquist Plots are given for Sm 2 Zr 2 O 7 . These materials have a definite band gap absorbing mainly in the UV region which makes them good candidates for photocatalysed dye degradation studies. Potential of some of these compositions as photocatalysts was also explored and they were found to efficiently catalyse the degradation of Xylenol Orange with t 1/2 decreasing from pure Sm 2 Zr 2 O 7 to pure Dy 2 Zr 2 O 7

A new molybdenum trioxide hydrate MoO3.1/3H2O and a new monoclinic form of MoO3

International Nuclear Information System (INIS)

Harb, F.; Gerand, B.; Nowogrocki, G.; Figlarz, M.

1986-01-01

A new hydrate of molybdenum trioxide MoO 3 .1/3H 2 O has been obtained by hydrothermal treatment at 110 0 C of either aqueous suspensions of MoO 3 .2H 2 O or aqueous molybdic acid solutions. The hydrate crystallizes in the orthorhombic system, lattice parameters are given; a structural model is proposed by comparison with the isostructural WO 3 .1/3H 2 O phase. The dehydration of MoO 3 .1/3H 2 O leads to a new anhydrous molybdenum trioxide, monoclinic, the structure of which is of ReO 3 type [fr

Photoluminescence properties of BaMoO4 amorphous thin films

International Nuclear Information System (INIS)

Marques, Ana Paula Azevedo; Melo, Dulce M.A. de; Longo, Elson; Paskocimas, Carlos A.; Pizani, Paulo S.; Leite, Edson R.

2005-01-01

BaMoO 4 amorphous and crystalline thin films were prepared from polymeric precursors. The BaMoO 4 was deposited onto Si wafers by means of the spinning technique. The structure and optical properties of the resulting films were characterized by FTIR reflectance spectra, X-ray diffraction (XRD), atomic force microscopy (AFM) and optical reflectance. The bond Mo-O present in BaMoO 4 was confirmed by FTIR reflectance spectra. XRD characterization showed that thin films heat-treated at 600 and 200 deg. C presented the scheelite-type crystalline phase and amorphous, respectively. AFM analyses showed a considerable variation in surface morphology by comparing samples heat-treated at 200 and 600 deg. C. The reflectivity spectra showed two bands, positioned at 3.38 and 4.37 eV that were attributed to the excitonic state of Ba 2+ and electronic transitions within MoO 2- 4 , respectively. The optical band gaps of BaMoO 4 were 3.38 and 2.19 eV, for crystalline (600 deg. C/2 h) and amorphous (200 deg. C/8 h) films, respectively. The room-temperature luminescence spectra revealed an intense single-emission band in the visible region. The PL intensity of these materials was increased upon heat-treatment. The excellent optical properties observed for BaMoO 4 amorphous thin films suggested that this material is a highly promising candidate for photoluminescent applications

Measurement of L-XRF cross-sections and Coster–Kronig enhancement factors for {sup 62}Sm at excitation energies 6.8, 7.4 and 8 KeV

Energy Technology Data Exchange (ETDEWEB)

Kumar, R., E-mail: rajiv_005@rediffmail.com [Department of Physics, HCTM Technical Campus, Kaithal, Haryana 136027 (India); Rani, A., E-mail: anita_teotia@rediffmail.com [Department of Physics, University P.G. College Kurukshetra, Kurukshetra University, Kurukshetra, Haryana 136119 (India); Singh, R.M. [Department of Physics, Ch. Devi Lal University, Sirsa, Haryana 125055 (India); Tiwari, M.K.; Singh, A.K. [X-ray Optics Section, Indus Synchrotron Utilization Division, Raja Ramanna Centre for Advanced Technology, Indore, Madhya Pradesh 452013 (India)

2016-05-15

Highlights: • L XRF production cross-sections for {sup 62}Sm at excitation energies 6.8, 7.4 and 8 KeV were measured. • Synchrotron radiations with Peltier cooled Si(Li) detector was employed. • Experimental L XRF cross sections are in good agreement with the theoretical estimations of Puri’s data. • The present study was also carried out to examine the effect of Coster - Kronig transitions on L XRF cross section. • The measured enhancement factors are found to be smaller than the theoretical estimations. - Abstract: L{sub ℓ}, L{sub α} and L{sub β} XRF production cross-sections were measured for {sup 62}Sm at excitation energies i.e. 6.8 KeV, 7.4 KeV and 8 KeV using synchrotron radiations. Experimental measurements were also carried out to examine the effect of Coster–Kronig transitions (non-radiative transitions) on fluorescence cross section for the L{sub i} (i = 1, 2, 3) X-ray lines. The experimental cross-sections with greater accuracy and better signal to noise ratio can be measured using a polarized monoenergetic excitation beam and a high resolution detector system. A Peltier cooled vortex solid state detector with energy resolution of 138 eV at 5.959 keV X-ray was employed. Experimentally measured cross-sections have been compared with the theoretical predictions with the data of M.O. Krause [J. Phys. Chem. Ref. Data 8 (1979) 307], J.L. Campbell [At. Data Nucl. Data Tables 85 (2003) 291] and S. Puri et al. [X-Ray Spectrom. 22 (1993) 358]. The measured enhancement factors were found to be smaller than the theoretically calculated values.

Enhanced visible light-responsive photocatalytic activity of LnFeO3 (Ln = La, Sm) nanoparticles by synergistic catalysis

International Nuclear Information System (INIS)

Li, Li; Wang, Xiong; Zhang, Yange

2014-01-01

Highlights: • LnFeO 3 (Ln = La, Sm) nanoparticles were prepared by a facile sol–gel method. • The samples exhibit superior visible-light-responsive photocatalytic activity. • Synergistic effect will enhance the photodegradation of RhB under visible light. - Abstract: LnFeO 3 (Ln = La, Sm) nanoparticles were prepared by a facile sol–gel method with assistance of glycol at different calcination temperatures. The as-synthesized LnFeO 3 was characterized by X-ray diffraction, transmission electron microscopy, differential scanning calorimeter and thermogravimetric analysis, and UV–vis absorption spectroscopy. The photocatalytic behaviors of LnFeO 3 nanoparticles were evaluated by photodegradation of rhodamine B under visible light irradiation. The results indicate that the visible light-responsive photocatalytic activity of LnFeO 3 nanoparticles was enhanced remarkably by the synergistic effect between the semiconductor photocatalysis and Fenton-like reaction. And a possible catalytic mechanism was also proposed based on the experimental results

Infrared luminescence and thermoluminescence of lithium borate glasses doped with Sm3+ ions

Directory of Open Access Journals (Sweden)

Anjaiah J.

2015-03-01

Full Text Available Thermoluminescence (TL characteristics of X-ray irradiated pure and doped with Sm3+ ions Li2O-MO-B2O3 (where MO=ZnO, CaO, CdO glasses have been studied in the temperature range of 303 to 573 K. All the pure glasses exhibited single TL peaks at 382 K, 424 K and 466 K. When these glasses were doped with Sm3+ ions no additional peaks have been observed but the glow peak temperature of the existing glow peak shifted gradually towards higher temperatures with gain in intensity of TL light output. The area under the glow curve was found to be maximum for Sm3+ doped glasses mixed with cadmium oxide as a modifier. The trap depth parameters associated with the observed TL peaks have been evaluated using Chen’s formulae. The possible use of these glasses in radiation dosimetry has been described. The results clearly showed that samarium doped cadmium borate glass has a potential to be considered as a thermoluminescence dosimeter.

Hydrodeoxygenation of bio-oil using different mesoporous supports of NiMo catalysts

Science.gov (United States)

Rinaldi, Nino; Simanungkalit, Sabar P.; Kristiani, Anis

2017-11-01

Biomass as a renewable and sustainable resources need to utilize in many applications, especially for energy application. One of its energy application is about converting biomass into bio-oil. High oxygen content in bio-oil needs to be upgraded through hydrodeoxygenation process before being used as transportation fuel. The development of heterogenenous catalysts become an important aspect in hydrodeoxygenation process, in particular the upgrading process of bio-oil. Several supporting mesoporous materials, such as TiO2, Al2O3 and MCM-41 have unique properties, both physical and chemical properties that can be utilized in various application, including catalyst. These heterogeneous catalysts were modified their catalytic properties by impregnation with some transition metal. The effect of various supporting material and transition metal impregnated were also studied. Their chemical and physical properties were characterized by X-Ray Diffraction, X-Ray Fluororesence, Fourier Transform Infra-Red, and Surface Area Analyzer. The result of characterizations showed that Ni-Mo/TiO2 is more crystalline than Ni-Mo/MCM-41 and Ni-Mo/Al2O3. In other hand, the specific surface area of Ni-Mo/TiO2 is lower than others. These heterogeneous catalysts were tested their catalytic activity in upgrading bio-oil. The liquid products produced were analyzed by using Elemental Analyzer. The result of catalytic activity tests showed catalysts resulted Ni-Mo/TiO2 exhibits best catalytic activity in hydrodeoxygenation process. The oxygen content decreased significantly from 41.61% to 26.22% by using Ni-Mo/TiO2. Compared with Ni-Mo/TiO2, Ni-Mo/MCM-41 and Ni-Mo/Al2O3 decrease lower to 33.22% % and 28.34%, respectively. Ni-Mo/TiO2 also resulted the highest Deoxygenation Degree (DOD) as of 55% compared with Ni-Mo/MCM-41 and Ni-Mo/Al2O3 as of 31.99 % and 47.99%, respectively.

Hybrid selective noncatalytic reduction (SNCR)/selective catalytic reduction (SCR) for NOx removal using low-temperature SCR with Mn-V2O5/TiO2 catalyst.

Science.gov (United States)

Choi, Sung-Woo; Choi, Sang-Ki; Bae, Hun-Kyun

2015-04-01

A hybrid selective noncatalytic reduction/selective catalytic reduction (SNCR/SCR) system that uses two types of technology, low-temperature SCR process and SNCR process, was designed to develop nitrogen oxide (NOx) reduction technology. SCR was conducted with space velocity (SV)=2400 hr(-1) and hybrid SNCR/SCR with SV=6000 hr(-1), since the study focused on reducing the amount of catalyst and both achieved 98% NOx reduction efficiency. Characteristics of NOx reduction by NH3 were studied for low-temperature SCR system at 150 °C using Mn-V2O5/TiO2 catalyst. Mn-added V2O5/TiO2 catalyst was produced, and selective catalyst reduction of NOx by NH3 was experimented. NOx reduction rate according to added Mn content in Mn-V2O5/TiO2 catalyst was studied with varying conditions of reaction temperature, normalized stoichiometric ratio (NSR), SV, and O2 concentration. In the catalyst experiment according to V2O5 concentration, 1 wt.% V2O5 catalyst showed the highest NOx reduction rate: 98% reduction at temperature window of 200~250 °C. As a promoter of the V2O5 catalyst, 5 wt.% Mn was added, and the catalyst showed 47~90% higher efficiency even with low temperatures, 100~200 °C. Mn-V2O5/TiO2 catalyst, prepared by adding 5 wt.% Mn in V2O5/TiO2 catalyst, showed increments of catalyst activation at 150 °C as well as NOx reduction. Mn-V2O5/TiO2 catalyst showed 8% higher rate for NOx reduction compared with V2O5/TiO2 catalyst in 150 °C SCR. Thus, (5 wt.%)Mn-(1 wt.%)V2O5/TiO2 catalyst was applied in SCR of hybrid SNCR/SCR system of low temperature at 150 °C. Low-temperature SCR hybrid SNCR/SCR (150 °C) system and hybrid SNCR/SCR (350 °C) showed 91~95% total reduction rate with conditions of SV=2400~6000 hr(-1) SCR and 850~1050 °C SNCR, NSR=1.5~2.0, and 5% O2. Hybrid SNCR/SCR (150 °C) system proved to be more effective than the hybrid SNCR/SCR (350 °C) system at low temperature. NOx control is very important, since they are the part of greenhouse gases as well as the

Synthesis and Photocatalytic Activity of Mo-Doped TiO2 Nanoparticles

Directory of Open Access Journals (Sweden)

Ji-guo Huang

2015-01-01

Full Text Available The undoped and Mo-doped TiO2 nanoparticles were synthesized by sol-gel method. The as-prepared samples were characterized by X-ray diffraction (XRD, diffuse reflectance UV-visible absorption spectra (UV-vis DRS, X-ray photoelectron spectra (XPS, and transmission electron microscopy (TEM. The photocatalytic activity was evaluated by photocatalytic degradation of methylene blue under irradiation of a 500 W xenon lamp and natural solar light outdoor. Effects of calcination temperatures and Mo doping amounts on crystal phase, crystallite size, lattice distortion, and optical properties were investigated. The results showed that most of Mo6+ took the place of Ti4+ in the crystal lattice of TiO2, which inhibited the growth of crystallite size, suppressed the transformation from anatase to rutile, and led to lattice distortion of TiO2. Mo doping narrowed the band gap (from 3.05 eV of TiO2 to 2.73 eV of TiMo0.02O and efficiently increased the optical absorption in visible region. Mo doping was shown to be an efficient method for degradation of methylene blue under visible light, especially under solar light. When the calcination temperature was 550°C and the Mo doping amount was 2.0%, the Mo-doped TiO2 sample exhibited the highest photocatalytic activity.

Study on the influence of nickel and Al{sub 2}O{sub 3} support on MoS{sub 2} as hydrodenitrogenation catalysts

Energy Technology Data Exchange (ETDEWEB)

Hein, J.; Hrabar, A.; Gutierrez, O.Y.; Lercher, J.A. [Technische Univ. Muenchen, Garching (Germany). Catalysis Research Center

2012-07-01

Alumina-supported Mo and Ni-Mo catalysts as well as an unsupported NiMo catalyst were characterized and tested in the hydrodenitrogenation (HDN) of quinoline in the presence of dibenzothiophene (DBT). The supported catalysts had a well dispersed MoS{sub 2} phase with an average stacking degree around two and slabs length below 10 nm. The unsupported NiMo sulfide catalyst exhibited long, multistacked MoS{sub 2} slabs and contained segregated Ni{sub x}S{sub y} phases. The formation of the Ni-Mo-S phase in both Ni containing catalysts was verified by X-ray absorption spectroscopy, whereas the concentration of coordinatively unsaturated sites was higher for the supported Mo and Ni-Mo catalysts than for the unsupported one. All catalysts were active in the HDN of quinoline and hydrodesulfurization of DBT. The catalytic activity increased in the order Mo/Al{sub 2}O{sub 3} < NiMo/unsupported < Ni-Mo/Al{sub 2}O{sub 3}. Thus, the influence on the catalytic activity of the promoter metal Ni is more important than the presence of a support due to the formation of the Ni-Mo-S phase (more active than MoS{sub 2}). (orig.)

Fabrication of Core-Shell Structural SiO2@H3[PM12O40] Material and Its Catalytic Activity

Directory of Open Access Journals (Sweden)

Xin Yang

2014-01-01

Full Text Available Through a natural tree grain template and sol-gel technology, the heterogeneous catalytic materials based on polyoxometalate compounds H3[PM12O40] encapsulating SiO2: SiO2@H3[PM12O40] (SiO2@PM12, M = W, Mo with core-shell structure had been prepared. The structure and morphology of the core-shell microspheres were characterized by the XRD, IR spectroscopy, UV-Vis absorbance, and SEM. These microsphere materials can be used as heterogeneous catalysts with high activity and stability for catalytic wet air oxidation of pollutant dyes safranine T (ST at room condition. The results show that the catalysts have excellent catalytic activity in treatment of wastewater containing 10 mg/L ST, and 94% of color can be removed within 60 min. Under different cycling runs, it is shown that the catalysts are stable under such operating conditions and the leaching tests show negligible leaching effect owing to the lesser dissolution.

FIA versatile system for spectrophotometric determinations of vanadium and molybdenum exploring the catalytic activities of V(V) and Mo(VI); Sistema FIA polivalente para determinacoes espectrofotometricas de vanadio e molibdenio explorando as atividades cataliticas de V(V) e Mo(VI)

Energy Technology Data Exchange (ETDEWEB)

Luca, Gilmara Caseri de

1996-02-01

A versatile system for chemical analysis by flow injection analysis was developed and applied for catalytic spectrophotometric determination of vanadium or molybdenum in metallic alloys. The selected methods were based upon indicator reactions chromotropic (CS)-bromate acid or hydrogen iodide-peroxide, respectively. Initially, a model system was proposed, in which common parameters for methods were studied. This included a re-sampling process in which high degrees of samples dilution were obtained. Other parameters such as concentrations and reagents addition order, reaction medium Ph, temperature and ionic power, as well as procedures for sample solubilization, were studied relating to each method. A mini-column with cationic exchanger resin (Dowex 50W-X8, 50-100 mesh, H{sup +} form) was used. The system for vanadium determination processes 120 samples by hour, consuming 2,0 mg CS and 10 mg K Br O{sub 3b}y determination. Concerning the method for molybdenum, the reagents consumption was 2,0 mg KI and 1,0 {mu}L of solution 30% H{sub 2}O{sub 2} by determination, since the analytic velocity was the same, in relation to vanadium.

Controlled synthesis of MoO3 microcrystals by subsequent calcination of hydrothermally grown pyrazine–MoO3 nanorod hybrids and their photodecomposition properties

International Nuclear Information System (INIS)

Rajagopal, S.; Nataraj, D.; Khyzhun, O.Y.; Djaoued, Yahia; Robichaud, Jacques; Kim, Chang-Koo

2013-01-01

We present our results on successful synthesis of pyrazine–MoO 3 nanorod hybrids by using pyrazine and MoO 3 nanorods. On the first stage, MoO 3 nanorods were grown hydrothermally and, on the second stage, their mixture with pyrazine was again involved in a hydrothermal reaction to produce organic–inorganic hybrids. To understand the growth mechanism of the hybrids we varied time and temperature of the hydrothermal process. Intercalation of pyrazine was confirmed through X-ray diffraction analysis, X-ray photoelectron spectroscopy, X-ray emission spectroscopy, scanning electron microscopy methods. Upon calcinations, pyrazine was deintercalated, i.e. removed from the MoO 3 hybrid system, and the MoO 3 nanorods were found to bind together resulting in formation of MoO 3 microslabs with increased surface area. Photodecomposition performance of the MoO 3 nanorods, pyrazine–MoO 3 hybrids and MoO 3 microcrystals was studied against Procion Red MX-5B textile dye. A high photodecomposition performance was found to decrease when going from MoO 3 nanorods to MoO 3 microcrystal and, further, to pyrazine–MoO 3 hybrids. - Graphical abstract: Display Omitted - Highlights: • High aspect ratio MoO 3 nanorods were prepared through a new hydrothermal method. • Hybrids of pyrazine–MoO 3 were formed by intercalating pyrazine into MoO 3 nanorods. • Intercalation of pyrazine was confirmed in X-ray spectroscopic analysis. • After calcinations, MoO 3 crystal was retained by binding MoO 3 nanorods together. • High photodegradation performance was noticed from MoO 3 nanorods

MoOx modified ZnGaO based transparent conducting oxides

Science.gov (United States)

Dutta, Titas; Gupta, P.; Bhosle, V.; Narayan, J.

2009-03-01

We report here the growth of high work function bilayered structures of thin MoOx (2.0MoOx layer, molybdenum exists in Mo4+, Mo5+, and Mo6+ oxidation states, and the ratio of (Mo4++Mo5+) to Mo6+ was determined to be ˜2:1. The bilayer films showed good optical transparency (≥80%) and low resistivity of ˜10-4 Ω cm. Different transport behavior of the MoOx/ZnGa0.05O films grown at different Ts (substrate temperature) was observed in temperature-dependent resistivity measurements. The bilayer film at higher Ts showed metallic conductivity behavior down to 113 K. Moreover, a blueshift of the absorption edge in the transmission spectrum was observed with the increase in Ts, indicating an increase in the carrier concentration. It was observed that the ZnGa0.05O films with ultrathin MoOx (˜1-2 nanometers) overlayer showed a higher work function (varying from 4.7 to 5.1 eV) as compared to the single layer ZnGa0.05O film work function (˜4.4 eV). A correlation between the surface work function and MoOx layer thickness is observed. The higher work function of the MoOx overlayer is envisaged to improve the transport of the carriers across the heterojunction in a solid state device, thus resulting an increase in device efficiency.

Synthesis and characterization of MoO3 films by acid hydrolysis of K2Mo4O13

International Nuclear Information System (INIS)

Hernan, L.; Morales, J.

1989-01-01

The behaviour of K 2 Mo 4 O 13 heated under reflux in an acid medium has been studied. A metastable polymorphic MoO 3 phase crystallizing in the hexagonal system was obtained. Lengthy treatment led to the formation of orthorhombic MoO 3 with the (010) planes perfectly oriented parallel to the substrate. SEM images do not support a topotactic mechanism for the successive transformations. The reactions involved probably take place through the polymerization of discrete units formed in the bulk solution

In situ catalytic growth of large-area multilayered graphene/MoS2 heterostructures

OpenAIRE

Fu, Wei; Du, Fei-Hu; Su, Juan; Li, Xin-Hao; Wei, Xiao; Ye, Tian-Nan; Wang, Kai-Xue; Chen, Jie-Sheng

2014-01-01

Stacking various two-dimensional atomic crystals on top of each other is a feasible approach to create unique multilayered heterostructures with desired properties. Herein for the first time, we present a controlled preparation of large-area graphene/MoS2 heterostructures via a simple heating procedure on Mo-oleate complex coated sodium sulfate under N2 atmosphere. Through a direct in situ catalytic reaction, graphene layer has been uniformly grown on the MoS2 film formed by the reaction of M...

A new oxomolybdate component extracted from the "virtual dynamic library" yielding the macrocyclic anion [(Mo(VI)(8)O(28))(4)(Mo(V)(2)O(2)S(2))(4)](24-).

Science.gov (United States)

Korenev, Vladimir S; Boulay, Antoine G; Dolbecq, Anne; Sokolov, Maxim N; Hijazi, Akram; Floquet, Sébastien; Fedin, Vladimir P; Cadot, Emmanuel

2010-11-01

A rare isomer of the {Mo(8)O(28)}(8-) anion has been trapped from an acidified aqueous solution of molybdate by using the {Mo(2)O(2)S(2)}(2+) oxothio cation as the linker and isolated as a part of a unique macrocyclic anion, which consists of four isopolyoxomolybdate fragments {Mo(8)O(28)} bridged by four {Mo(2)O(2)S(2)} units.

Characterization of ultra-thin TiO2 films grown on Mo(112)

International Nuclear Information System (INIS)

Kumar, D.; Chen, M.S.; Goodman, D.W.

2006-01-01

Ultra-thin TiO 2 films were grown on a Mo(112) substrate by stepwise vapor depositing of Ti onto the sample surface followed by oxidation at 850 K. X-ray photoelectron spectroscopy showed that the Ti 2p peak position shifts from lower to higher binding energy with an increase in the Ti coverage from sub- to multilayer. The Ti 2p peak of a TiO 2 film with more than a monolayer coverage can be resolved into two peaks, one at 458.1 eV corresponding to the first layer, where Ti atoms bind to the substrate Mo atoms through Ti-O-Mo linkages, and a second feature at 458.8 eV corresponding to multilayer TiO 2 where the Ti atoms are connected via Ti-O-Ti linkages. Based on these assignments, the single Ti 2p 3/2 peak at 455.75 eV observed for the Mo(112)-(8 x 2)-TiO x monolayer film can be assigned to Ti 3+ , consistent with our previous results obtained with high-resolution electron energy loss spectroscopy

Quality of Metal Deposited Flux Cored Wire With the System Fe-C-Si-Mn-Cr-Mo-Ni-V-Co

Science.gov (United States)

Gusev, Aleksander I.; Kozyrev, Nikolay A.; Osetkovskiy, Ivan V.; Kryukov, Roman E.; Kozyreva, Olga A.

2017-10-01

Studied the effect of the introduction of vanadium and cobalt into the charge powder fused wire system Fe-C-Si-Mn-Cr-Ni-Mo-V, used in cladding assemblies and equipment parts and mechanisms operating under abrasive and abrasive shock loads. the cored wires samples were manufactured in the laboratory conditions and using appropriate powder materials and as a carbonfluoride contained material were used the dust from gas purification of aluminum production, with the following components composition, %: Al2O3 = 21-46.23; F = 18-27; Na2O = 8-15; K2O = 0.4-6; CaO = 0.7-2.3; Si2O = 0.5-2.48; Fe2O3 = 2.1-3.27; C = 12.5-30.2; MnO = 0.07-0.9; MgO = 0.06-0.9; S = 0.09-0.19; P = 0.1-0.18. Surfacing was produced on the St3 metal plates in 6 layers under the AN-26C flux by welding truck ASAW-1250. Cutting and preparation of samples for research had been implemented. The chemical composition and the hydrogen content of the weld metal were determined by modern methods. The hardness and abrasion rate of weld metal had been measured. Conducted metallographic studies of weld metal: estimated microstructure, grain size, contamination of oxide non-metallic inclusions. Metallographic studies showed that the microstructure of the surfaced layer by cored wire system Fe-C-Si-Mn-Cr-Mo-Ni-V-Co is uniform, thin dendrite branches are observed. The microstructure consists of martensite, which is formed inside the borders of the former austenite grain retained austenite present in small amounts in the form of separate islands, and thin layers of δ-ferrite, which is located on the borders of the former austenite grains. Carried out an assessment the effect of the chemical composition of the deposited metal on the hardness and wear and hydrogen content. In consequence of multivariate correlation analysis, it was determined dependence to the hardness of the deposited layer and the wear resistance of the mass fraction of the elements included in the flux-cored wires of the system Fe-C-Si-Mn-Cr-Mo-Ni-V

MnMoO4 nanolayers : Synthesis characterizations and electrochemical detection of QA

Science.gov (United States)

Muthamizh, S.; Kumar, S. Praveen; Munusamy, S.; Narayanan, V.

2018-04-01

MnMoO4 nanolayers were prepared by precipitation method. The MnMoO4 nanolayers were synthesized by using commercially available (CH3COO)2Mn.4H2O and Na2WO4.2H2O. The XRD pattern reveals that the synthesized MnMoO4 has monoclinic structure. In addition, lattice parameter values were also calculated using XRD data. The Raman analysis confirm the presence of Mo-O in MnMoO4 nanolayers. DRS-UV analysis shows that MnMoO4 has a band gap of 2.59 eV. FE-SEM and HR-TEM analysis along with EDAX confirms the material morphology in stacked layers like structure in nano scale. Synthesized nanolayers were utilized for the detection of biomolecule quercetin (QA).

Effect of RE (Nd3+, Sm3+) oxide on structural, optical properties of Na2O-Li2O-ZnO-B2O3 glass system

Science.gov (United States)

Hivrekar, Mahesh M.; Bhoyar, D. N.; Mande, V. K.; Dhole, V. V.; Solunke, M. B.; Jadhav, K. M.

2018-05-01

Zinc borate glass activated with rare earth oxide (Nd2O3, Sm2O3) of Na2O-Li2O-ZnO-B2O3 quaternary system has been prepared successfully by melt quenching method. The nucleation and growth of RE oxide were controlled temperature range 950-1000° C and rapid cooling at room temperature. The physical, structural and optical properties were characterized by using X-ray diffraction (XRD), SEM, Ultraviolet-visible spectroscopy (UV-Vis). XRD and SEM studies confirmed the amorphous nature, surface morphology of prepared zinc borate glass. The physical parameters like density, molar volume, molar mass of Nd3+, Sm3+ doped borate glass are summarized in the present article. The optical absorption spectra along with tauc's plot are presented. The optical energy band gap increases due to the addition of rare earth oxide confirming the role of network modifier.

Catalytic activity of Co/SiO2 and Co/TiO2 nanosized systems in the oxidation of carbon monoxide

Science.gov (United States)

Kelyp, A. A.; Smirnova, N. P.; Oleksenko, L. P.; Lutsenko, L. V.; Oranskaya, E. I.; Ripko, A. P.

2013-06-01

The effects of the preparation procedure, active component concentration, and conditions of formation of nanosized cobalt-containing systems based on TiO2 and SiO2 mesoporous powders on their catalytic activity in the oxidation of carbon monoxide were studied. The active phase in the systems was cobalt spinel CoCo2O4 found in all samples. High catalytic activity was found in the samples characterized by relatively high contents of surface active centers (cobalt cations with octahedral surroundings).

Orthorhombic MoO{sub 3} nanobelts based NO{sub 2} gas sensor

Energy Technology Data Exchange (ETDEWEB)

Mane, A.A. [Thin Film Nanomaterials Laboratory, Department of Physics, Shivaji University, Kolhapur 416 004 (India); General Science and Humanities Department, Sant Gajanan Maharaj College of Engineering, Mahagaon, 416 503 (India); Moholkar, A.V., E-mail: avmoholkar@gmail.com [Thin Film Nanomaterials Laboratory, Department of Physics, Shivaji University, Kolhapur 416 004 (India)

2017-05-31

Highlights: • The effect of thickness on physicochemical and NO{sub 2} gas sensing properties of sprayed MoO{sub 3} nanobelts has been reported. • The sprayed MoO{sub 3} nanobelts show the NO{sub 2} gas response of 68% for 100 ppm concentration at an operating temperature of 200 °C. • The lower detection limit of MoO{sub 3} nanobelts based NO{sub 2} sensor is found to be half of the IDLH value (20 ppm). - Abstract: Molybdenum trioxide (MoO{sub 3}) nanobelts have been deposited onto the glass substrates using chemical spray pyrolysis (CSP) deposition method. The XRD patterns reveal that films are polycrystalline having an orthorhombic crystal structure. Raman spectra confirm that the films are orthorhombic in phase. The XPS study shows the presence of two well resolved spectral lines of Mo-3d core levels appearing at the binding energy values of 232.82 eV and 235.95 eV corresponding to Mo-3d{sub 5/2} and Mo-3d{sub 3/2}, respectively. These binding energy values are assigned to Mo{sup 6+} oxidation state of fully oxidized MoO{sub 3}. The FE-SEM micrographs show the formation of nanobelts-like morphology. The AFM micrographs reveal that the RMS surface roughness increases from 16.5 nm to 17.5 nm with increase in film thickness from 470 nm to 612 nm and then decreases to 16 nm for 633 nm film thickness. The band gap energy is found to be decreased from 3.40 eV to 3.38 eV. To understand the electronic transport phenomenon in MoO{sub 3} thin films, dielectric properties are studied. For 612 nm film thickness, the highest NO{sub 2} gas response of 68% is obtained at an operating temperature of 200 °C for 100 ppm concentration with response and recovery times of 15 s and 150 s, respectively. The lower detection limit is found to be 10 ppm which is half of the immediately dangerous to life or health (IDLH) value of 20 ppm. Finally, NO{sub 2} gas sensing mechanism in an orthorhombic MoO{sub 3} crystal structure is discussed in detail.

On the reduction of orthorhombic MoO3 to MoO2

International Nuclear Information System (INIS)

Delannay, F.

1982-01-01

Electron diffraction shows evidence of topotactic orientation relationships between the original MoO 3 crystal and MoO 2 crystals formed under mild reduction conditions. These relationships differ from previously published literature data. A possible mechanism of formation of the [100] strings of edge sharing octahedra in the MoO 2 structure is tentatively proposed. (author)

Transfer matrix approach to electron transport in monolayer MoS2/MoO x heterostructures

Science.gov (United States)

Li, Gen

2018-05-01

Oxygen plasma treatment can introduce oxidation into monolayer MoS2 to transfer MoS2 into MoO x , causing the formation of MoS2/MoO x heterostructures. We find the MoS2/MoO x heterostructures have the similar geometry compared with GaAs/Ga1‑x Al x As semiconductor superlattice. Thus, We employ the established transfer matrix method to analyse the electron transport in the MoS2/MoO x heterostructures with double-well and step-well geometries. We also considere the coupling between transverse and longitudinal kinetic energy because the electron effective mass changes spatially in the MoS2/MoO x heterostructures. We find the resonant peaks show red shift with the increasing of transverse momentum, which is similar to the previous work studying the transverse-momentum-dependent transmission in GaAs/Ga1‑x Al x As double-barrier structure. We find electric field can enhance the magnitude of peaks and intensify the coupling between longitudinal and transverse momentums. Moreover, higher bias is applied to optimize resonant tunnelling condition to show negative differential effect can be observed in the MoS2/MoO x system.

Effects of synthesis conditions on structure and surface properties of SmMn{sub 2}O{sub 5} mullite-type oxide

Energy Technology Data Exchange (ETDEWEB)

Thampy, Sampreetha; Ibarra, Venessa; Lee, Yun-Ju [Department of Materials Science and Engineering, University of Texas at Dallas, Richardson, TX 75080 (United States); McCool, Geoffrey [Nanostellar Inc., 3696 Haven Avenue, Redwood City, CA 94063 (United States); Cho, Kyeongjae [Department of Materials Science and Engineering, University of Texas at Dallas, Richardson, TX 75080 (United States); Hsu, Julia W.P., E-mail: jwhsu@utdallas.edu [Department of Materials Science and Engineering, University of Texas at Dallas, Richardson, TX 75080 (United States)

2016-11-01

Highlights: • Investigate the effects of calcination temperature and precipitation pH on crystallinity, phase purity, particle size, surface composition, and NO adsorption capacity of SmMn{sub 2}O{sub 5}. • High calcination temperature increases mullite phase purity but decreases specific surface area (SSA). • Mullite phase purity is independent of pH while SSA monotonically increases. • SSA and surface Mn/Sm ratio determine NO uptake. - Abstract: A mixed-phase compound that contains SmMn{sub 2}O{sub 5} mullite-type oxides has been reported to display excellent catalytic activity for nitric oxide (NO) oxidation. Here we investigate the effects of calcination temperature and precipitation pH on structural, physical, chemical, and surface properties of SmMn{sub 2}O{sub 5}. As the calcination temperature increases from 750 °C to 1000 °C, mullite phase purity increases from 74% to 100%, while specific surface area (SSA) decreases from 23.6 m{sup 2}/g to 5.1 m{sup 2}/g with particle size increases correspondingly. Mullite phase purity (87%) is independent of pH between 8.5–10.4, whereas SSA monotonically increases from 12.5 m{sup 2}/g at pH 8.1 to 27.4 m{sup 2}/g at pH 13. X-ray photoelectron spectroscopy (XPS) studies reveal that the surface Mn/Sm ratio is similar to the bulk value and is unaffected by calcination temperature and pH values up to 10.4, whereas sample precipitated at pH 13 is surface-rich in Sm. NO chemisorption studies show that the SSA and surface Mn/Sm ratio determine NO uptake by SmMn{sub 2}O{sub 5} mullite oxides.

MoO3 incorporation in magnesium aluminosilicate glasses

International Nuclear Information System (INIS)

Tan, Shengheng; Ojovan, Michael I.; Hyatt, Neil C.; Hand, Russell J.

2015-01-01

Molybdate has a very low solubility in silicate and borosilicate glass systems and its excess presence in nuclear waste glass can cause the formation of a readily soluble “yellow phase”. In this study, the incorporation of molybdenum oxide (MoO 3 ) in a magnesium aluminosilicate glass system has been investigated. The prepared glasses show a higher than 90% molybdenum retention rate and up to 5.34 mol% (12.28 wt%) MoO 3 can be incorporated into these glasses without causing visible phase separation. The incorporation of MoO 3 increases glass density, decreases glass transition and crystallisation temperatures and intensifies Raman bands assigned to vibrations of MoO 4 2− units. When excess molybdate is added liquid–liquid phase separation and crystallisation occurs. The separated phase is spherical, 200–400 nm in diameter and randomly dispersed. Based on powder X-ray diffraction, Raman spectroscopy and transmission electron microscopy, the separated phase is identified as MgMoO 4

Electron beam-induced structural transformations of MoO{sub 3} and MoO{sub 3-x} crystalline nanostructures

Energy Technology Data Exchange (ETDEWEB)

Diaz-Droguett, D. E., E-mail: dodiaz@fis.puc.cl [Pontificia Universidad Catolica de Chile, Departamento de Fisica, Facultad de Fisica (Chile); Zuniga, A. [Universidad de Chile, Departamento de Ingenieria Mecanica, Facultad de Ciencias Fisicas y Matematicas (Chile); Solorzano, G. [PUC-RIO, Departamento de Ciencia dos Materiais e Metalurgia, DCMM (Brazil); Fuenzalida, V. M. [Universidad de Chile, Departamento de Fisica, Facultad de Ciencias Fisicas y Matematicas (Chile)

2012-01-15

Electron beam-induced damage and structural changes in MoO{sub 3} and MoO{sub 3-x} single crystalline nanostructures were revealed by in situ transmission electron microscopy (TEM) examination (at 200 kV) after few minutes of concentrating the electron beam onto small areas (diameters between 25 and 200 nm) of the samples. The damage was evaluated recording TEM images, while the structural changes were revealed acquiring selected area electron diffraction patterns and high resolution transmission electron microscopy (HRTEM) images after different irradiation times. The as-received nanostructures of orthorhombic MoO{sub 3} were transformed to a Magneli's phase of the oxide ({gamma}-Mo{sub 4}O{sub 11}) after {approx}10 min of electron beam irradiation. The oxygen loss from the oxide promoted structural changes. HRTEM observations showed that, in the first stage of the reduction, oxygen vacancies generated by the electron beam are accommodated by forming crystallographic shear planes. At a later stage of the reduction process, a polycrystalline structure was developed with highly oxygen-deficient grains. The structural changes can be attributed to the local heating of the irradiated zone combined with radiolysis.

Diodes based on semi-insulating CdTe crystals with Mo/MoO{sub x} contacts for X- and γ-ray detectors

Energy Technology Data Exchange (ETDEWEB)

Maslyanchuk, O.; Kulchynsky, V.; Solovan, M. [Chernivtsi National University, Chernivtsi (Ukraine); Gnatyuk, V. [Institute of Semiconductor Physics, NAS of Ukraine, Kyiv (Ukraine); Potiriadis, C. [Greek Atomic Energy Commission, Attiki (Greece); Kaissas, I. [Greek Atomic Energy Commission, Attiki (Greece); Department of Electrical and Computer Engineering, Aristotle University of Thessaloniki (Greece); Brus, V. [Helmholtz-Zentrum Berlin fuer Materialien und Energie GmbH, Berlin (Germany)

2017-03-15

This paper reports on the possible applications of molybdenum oxide (Mo/MoO{sub x}) contacts in combination with semi-insulating CdTe crystals. The electrical contacts to p-type Cl-doped CdTe crystals were formed by the deposition of molybdenum oxide and pure molybdenum thin films by the DC reactive magnetron sputtering. Electrical properties of the prepared Mo-MoO{sub x}/p-CdTe/MoO{sub x}-Mo surface-barrier structures were investigated at different temperatures. It is shown that the rapid growth of the reverse current with increasing bias voltage higher than 10 V is caused by the space-charge limited currents. Spectrometric properties of the Mo-MoO{sub x}/p-CdTe/MoO{sub x}-Mo structures have been also analyzed. It is revealed that the developed heterojunction has shown promising characteristics for its practical application in X- and γ-ray radiation detector fabrication. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Quaternary system LiF-LiCl-LiVO3-Li2MoO4

International Nuclear Information System (INIS)

Anipchenko, B.V.; Garkushin, I.K.

2000-01-01

Interactions in the LiF-LiCl-LiVO 3 -Li 2 MoO 4 system are studied by differential thermal analysis. Rate of heating/cooling of the samples comprised 15 Grad/min, mass of sample composed 0.2 g. The system was investigated in the 300-650 Deg C range. X-ray diffraction method was used for determination of purity of the reagents. Composition and temperature of quaternary component eutectics are determined: 16.5 mol. % of LiF, 47.0 mol. % of LiCl, 28.8 mol. % of LiVO 3 , 7.6 mol. % of Li 2 MoO 4 ; 387 Deg C. Mean value of melting enthalpy of quaternary eutectics mixture in the LiF-LiCl-LiVO 3 -Li 2 MoO 4 system on the results of the tests was in the range of 222 kJ/kg [ru

Comparative study on cubic and tetragonal CexZr1-xO2 supported MoO3-catalysts for sulfur-resistant methanation

Science.gov (United States)

Liu, Zhaopeng; Xu, Yan; Cheng, Jiaming; Wang, Weihan; Wang, Baowei; Li, Zhenhua; Ma, Xinbin

2018-03-01

In this paper, two kinds of CexZr1-xO2 solid solution carriers with different Ce/Zr ratio were prepared by one-step co-precipitation method: the cubic Ce0.8Zr0.2O2 and the tetragonal Ce0.2Zr0.8O2 support. The MoO3/Ce0.8Zr0.2O2 and MoO3/Ce0.2Zr0.8O2 catalysts were prepared by incipient wetness impregnation method for comparative study on sulfur-resistant methanation reaction. The N2 adsorption/desorption, X-ray diffraction (XRD), Raman spectroscopy (RS), X-ray photoelectron (XPS), transmission electron microscopy (TEM), temperature-programmed reduction by hydrogen (H2-TPR) were undertaken to characterize the physico-chemical properties of the samples. The results indicated that the prepared MoO3/CexZr1-xO2 catalysts have a mesoporous structure with high surface area and uniform pore size distribution, achieving good MoO3 dispersion on CexZr1-xO2 supports. As for the catalytic performance of sulfur-resistant methanation, the cubic MoO3/Ce0.8Zr0.2O2 exhibited better than the tetragonal MoO3/Ce0.2Zr0.8O2 catalyst at reaction temperature 400 °C and 450 °C. CO conversion on the cubic MoO3/Ce0.8Zr0.2O2 catalyst was 50.1% at 400 °C and 75.5% at 450 °C, which is respectively 7% and 20% higher than that on the tetragonal MoO3/Ce0.2Zr0.8O2 catalyst. These were mainly attributed to higher content of active MoS2 on the surface of catalyst, the enhanced oxygen mobility, increased Mo-species dispersion as well as the excellent reducibility resulted from the increased amount of the reducible Ce3+ on the cubic MoO3/Ce0.8Zr0.2O2 catalyst.

Guided ion beam and theoretical studies of the bond energy of SmS+

Science.gov (United States)

Armentrout, P. B.; Demireva, Maria; Peterson, Kirk A.

2017-12-01

Previous work has shown that atomic samarium cations react with carbonyl sulfide to form SmS+ + CO in an exothermic and barrierless process. To characterize this reaction further, the bond energy of SmS+ is determined in the present study using guided ion beam tandem mass spectrometry. Reactions of SmS+ with Xe, CO, and O2 are examined. Results for collision-induced dissociation processes with all three molecules along with the endothermicity of the SmS+ + CO → Sm+ + COS exchange reaction are combined to yield D0(Sm+-S) = 3.37 ± 0.20 eV. The CO and O2 reactions also yield a SmSO+ product, with measured endothermicities that indicate D0(SSm+-O) = 3.73 ± 0.16 eV and D0(OSm+-S) = 1.38 ± 0.27 eV. The SmS+ bond energy is compared with theoretical values characterized at several levels of theory, including CCSD(T) complete basis set extrapolations using all-electron basis sets. Multireference configuration interaction calculations with explicit spin-orbit calculations along with composite thermochemistry using the Feller-Peterson-Dixon method and all-electron basis sets were also explored for SmS+, and for comparison, SmO, SmO+, and EuO.

A calorimetric and thermodynamic investigation of A2[(UO2)2(MoO4)O2] compounds with A = K and Rb and calculated phase relations in the system (K2MoO4 + UO3 + H2O)

International Nuclear Information System (INIS)

Lelet, Maxim I.; Suleimanov, Evgeny V.; Golubev, Aleksey V.; Geiger, Charles A.; Bosbach, Dirk; Alekseev, Evgeny V.

2015-01-01

Highlights: • We determined the low temperature heat capacity of A 2 [(UO 2 ) 2 (MoO 4 )O 2 ] compounds with A = K and Rb. • We determined enthalpy of formation of K 2 [(UO 2 ) 2 (MoO 4 )O 2 ] by HF solution calorimetry. • We calculated Δ f G° (T = 298 K) of all phases from studied series. • Using obtained data we performed a thermodynamic modelling in the system (K 2 MoO 4 + UO 3 + H 2 O). - Abstract: A calorimetric and thermodynamic investigation of two alkali-metal uranyl molybdates with general composition A 2 [(UO 2 ) 2 (MoO 4 )O 2 ], where A = K and Rb, was performed. Both phases were synthesized by solid-state sintering of a mixture of potassium or rubidium nitrate, molybdenum (VI) oxide and gamma-uranium (VI) oxide at high temperatures. The synthetic products were characterised by X-ray powder diffraction and X-ray fluorescence methods. The enthalpy of formation of K 2 [(UO 2 ) 2 (MoO 4 )O 2 ] was determined using HF-solution calorimetry giving Δ f H° (T = 298 K, K 2 [(UO 2 ) 2 (MoO 4 )O 2 ], cr) = −(4018 ± 8) kJ · mol −1 . The low-temperature heat capacity, C p °, was measured using adiabatic calorimetry from T = (7 to 335) K for K 2 [(UO 2 ) 2 (MoO 4 )O 2 ] and from T = (7 to 326) K for Rb 2 [(UO 2 ) 2 (MoO 4 )O 2 ]. Using these C p ° values, the third law entropy at T = 298.15 K, S°, is calculated as (374 ± 1) J · K −1 · mol −1 for K 2 [(UO 2 ) 2 (MoO 4 )O 2 ] and (390 ± 1) J · K −1 · mol −1 for Rb 2 [(UO 2 ) 2 (MoO 4 )O 2 ]. These new experimental results, together with literature data, are used to calculate the Gibbs energy of formation, Δ f G°, for both phases giving: Δ f G° (T = 298 K, K 2 [(UO 2 ) 2 (MoO 4 )O 2 ], cr) = (−3747 ± 8) kJ · mol −1 and Δ f G° (T = 298 K, Rb 2 [(UO 2 ) 2 (MoO 4 )], cr) = −3736 ± 5 kJ · mol −1 . Smoothed C p °(T) values between 0 K and 320 K are presented, along with values for S° and the functions [H°(T) − H°(0)] and [G°(T) − H°(0)], for both phases. The

Effects of Sm3+/Yb3+ co-doping and temperature on the Raman, IR spectra and structure of [TeO2-GeO2-K2O-Sm2O3/Yb2O3] glasses

International Nuclear Information System (INIS)

Shaltout, I.; Badr, Y.

2006-01-01

Effects of Sm 3+ /Yb 3+ co-doping on Raman scattering, IR absorption, temperature dependence of the Raman spectra up to 210 o C and the structure of two glass systems of the composition (80TeO 2 -10GeO 2 -8K 2 O-2Sm 2 O 3 /Yb 2 O 3 ) is discussed. It was found that the addition of Yb 3+ to the glass very strongly enhances the intensities of the antistokes' Raman bands at 155, 375, 557 and 828 cm -1 and quenches both the intensities of the stokes' vibration modes of the TeO 4 units in the range of 120-770 cm -1 and the intensities of the OH - stretching vibration modes in the range of 2600-3300 cm -1 . Sm 2 O 3 /Yb 2 O 3 rare earth co-doping has a great influence on removing and/or changing the nature of the OH - groups. The appearance and splitting of the stretching vibration modes of the OH - groups at lower frequencies (2770, 2970 cm -1 ) for the Sm +3 singly doped glass sample, compared to the band at ∼3200 cm -1 for the Sm 3+ /Yb 3+ co-doped glass sample, suggested that the OH - groups are more strongly bonded and incorporated with the glass matrix for the singly doped glass. Heating the sample up continuously weakens the hydrogen bonding of the OH - groups to the glass matrix leading to creation of NBO and breakdown of the connectivity of the OH - groups to the TeO 4 , TeO 3+1 and TeO 3 structural units. Raman bands at 286, 477, 666 and 769 cm -1 were assigned to its respective vibrations of Te 2 O 7 , TeO 4 -4 species, the (Te-O-Te) bending vibrations of the TeO 4 triagonal bipyramids (tbps), the axial symmetric stretching vibration modes (Te ax -O) s with bridging oxygen BO atoms and to the (Te-O) nbo non-bridging stretching vibration modes of the TeO 3+1 and/or TeO 3 pyramids

Holey Reduced Graphene Oxide Coupled with an Mo2 N-Mo2 C Heterojunction for Efficient Hydrogen Evolution.

Science.gov (United States)

Yan, Haijing; Xie, Ying; Jiao, Yanqing; Wu, Aiping; Tian, Chungui; Zhang, Xiaomeng; Wang, Lei; Fu, Honggang

2018-01-01

An in situ catalytic etching strategy is developed to fabricate holey reduced graphene oxide along with simultaneous coupling with a small-sized Mo 2 N-Mo 2 C heterojunction (Mo 2 N-Mo 2 C/HGr). The method includes the first immobilization of H 3 PMo 12 O 40 (PMo 12 ) clusters on graphite oxide (GO), followed by calcination in air and NH 3 to form Mo 2 N-Mo 2 C/HGr. PMo 12 not only acts as the Mo heterojunction source, but also provides the Mo species that can in situ catalyze the decomposition of adjacent reduced GO to form HGr, while the released gas (CO) and introduced NH 3 simultaneously react with the Mo species to form an Mo 2 N-Mo 2 C heterojunction on HGr. The hybrid exhibits superior activity towards the hydrogen evolution reaction with low onset potentials of 11 mV (0.5 m H 2 SO 4 ) and 18 mV (1 m KOH) as well as remarkable stability. The activity in alkaline media is also superior to Pt/C at large current densities (>88 mA cm -2 ). The good activity of Mo 2 N-Mo 2 C/HGr is ascribed to its small size, the heterojunction of Mo 2 N-Mo 2 C, and the good charge/mass-transfer ability of HGr, as supported by a series of experiments and theoretical calculations. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Cathodic Electrodeposition of Ni-Mo on Semiconducting NiFe2 O4 for Photoelectrochemical Hydrogen Evolution in Alkaline Media.

Science.gov (United States)

Wijten, Jochem H J; Jong, Ronald P H; Mul, Guido; Weckhuysen, Bert M

2018-04-25

Photocathodes for hydrogen evolution from water were made by electrodeposition of Ni-Mo layers on NiFe 2 O 4 substrates, deposited by spin coating on F:SnO 2 -glass. Analysis confirmed the formation of two separate layers, without significant reduction of NiFe 2 O 4 . Bare NiFe 2 O 4 was found to be unstable under alkaline conditions during (photo)electrochemistry. To improve the stability significantly, the deposition of a bifunctional Ni-Mo layer through a facile electrodeposition process was performed and the composite electrodes showed stable operation for at least 1 h. Moreover, photocurrents up to -2.1 mA cm -2 at -0.3 V vs. RHE were obtained for Ni-Mo/NiFe 2 O 4 under ambient conditions, showing that the new combination functions as both a stabilizing and catalytic layer for the photoelectrochemical evolution of hydrogen. The photoelectrochemical response of these composite electrodes decreased with increasing NiFe 2 O 4 layer thickness. Transient absorption spectroscopy showed that the lifetime of excited states is short and on the ns timescale. An increase in lifetime was observed for NiFe 2 O 4 of large layer thickness, likely explained by decreasing the defect density in the primary layer(s), as a result of repetitive annealing at elevated temperature. The photoelectrochemical and transient absorption spectroscopy results indicated that a short charge carrier lifetime limits the performance of Ni-Mo/NiFe 2 O 4 photocathodes. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Sr_2SmNbO_6 perovskite: Synthesis, characterization and density functional theory calculations

International Nuclear Information System (INIS)

Dutta, Alo; Mukhopadhyay, P.K.; Sinha, T.P.; Shannigrahi, Santiranjan; Himanshu, A.K.; Sen, Pintu; Bandyopadhyay, S.K.

2016-01-01

The density functional theory (DFT) under the generalized gradient approximation (GGA) has been used to investigate the electronic structure of double perovskite oxide Sr_2SmNbO_6 synthesized by the solid-state reaction technique. The Rietveld refinement of the X-ray diffraction pattern of the sample shows the monoclinic P2_1/n phase at room temperature. The X-ray photoemission spectrum (XPS) of the material is collected in the energy window of 0–1200 eV. The chemical shift of the constituent elements calculated from the core level XPS spectra is used to analyze the covalency between the O anion and Sm/Nb cations. The valence band (VB) XPS spectrum is compared with the calculated VB spectrum using partial density of states in a standard way. The Raman spectrum is employed to investigate the phonon modes of the material in the monoclinic phase. Lorentzian lines are used to fit the experimental Raman spectrum, which present 24 phonon modes corresponding to the stretching and banding of NbO_6/SmO_6 octahedra and translational motion of Sr along the Sr−O bond. The discrepancy between the measured and calculated band gap values has been removed by applying modified Becke-Johnson (mBJ) potential in the DFT calculations. The experimental optical band gap obtained from the UV–visible reflectance spectrum is found to be 3.42 eV, which is well matched with the DFT calculated value of 3.2 eV, and suggests the semiconducting nature of the material. The real (ε′) and imaginary (ε″) parts of the optical dielectric constant as a function of energy along the x-, y- and z-polarization directions using mBJ potential are calculated. The collective vibrational modes of the atoms, the Born effective charge of the ions and their effect on the static dielectric constant of the material are studied using DFT. The calculated value of static dielectric constant for SSN is found to be 41.3. - Highlights: • Electronic structure and dynamical properties of Sr_2SmNbO_6 (SSN

Determination and modeling for the solubility of Na_2MoO_4·2H_2O in the (Na"+ + MoO_4"2"− + SO_4"2"−) system

International Nuclear Information System (INIS)

Ning, Pengge; Xu, Weifeng; Cao, Hongbin; Lin, Xiao; Xu, Hongbin

2016-01-01

Highlights: • The solubility of Na_2MoO_4·2H_2O in Na"+ + MoO_4"2"− + SO_4"2"− system was performed. • The new model was established via regressing the published and the determined data. • The Pitzer parameter and the solubility product constant of the salts in solution were calculated. • The model was applied to estimate the solubility of the sodium molybdate in various conditions. - Abstract: The solubility of Na_2MoO_4·2H_2O in (Na"+ + MoO_4"2"− + SO_4"2"−) system was carried out using a dynamic method within the temperature range from 293.15 K to 343.15 K. The new model was established via regression of the published and the determined values to predict the solubility. From the results, the solubility of sodium molybdate increases with the temperature increase, however, it decreases with the increasing concentration of sodium sulfate. The Pitzer parameters and the solubility product constant of sodium sulfate and sodium molybdate in aqueous solution were obtained using the literature data. The solubilities of the sodium molybdate in the sodium sulfate solution as well as the thermodynamic parameters were calculated based on the experimental values obtained. The new model was also applied to estimate the solubility of the sodium molybdate under various conditions. The calculated values agree well with the experiment results.

Heavy-water (D2O) take-up-induced lattice expansion in the high-temperature proton conductor Ba3Ca1.18Nb1.82O9-δ

International Nuclear Information System (INIS)

Papathanassopoulos, K.; Wenzl, H.; Schober, T.

1997-01-01

Dimensional changes of the high-temperature proton conductor Ba 3 Ca 1.18 Nb 1.82 O 9-δ , when exposed to D 2 O vapor, were investigated using length-change and precision density measurements. Such information is essential for possible applications of proton conductors in solid oxide fuel cells and humidity and hydrogen sensors. A linear increase of the sample lengths with increases in the deuterium content was observed. Comparison of the present D 2 O data with those that were previously obtained for H 2 O showed that there was a small isotope effect in the lattice expansion. The fact that the length-change-versus-hydrogen-isotope-concentration curves were almost isotope independent supported the validity of the take-up reaction H 2 O(g) + V sm-bulletsm-bullet O + O x O right-reversible 2OH sm-bullet O , where V O is the vacancies in the oxygen sublattice and OH sm-bullet O is the proton that are embedded in the electron cloud of an oxygen atom. In regard to the latter equation, it was found that small islands of silver, palladium, nickel, and platinum act as catalytic promoters of the reaction and lead, for given heavy-water-steam exposure conditions, to an increase of water absorption of up to 100%, when compared with samples without the catalytic surface layers

Facile Synthesis of In–Situ Nitrogenated Graphene Decorated by Few–Layer MoS2 for Hydrogen Evolution Reaction

International Nuclear Information System (INIS)

Dai, Xiaoping; Li, Zhanzhao; Du, Kangli; Sun, Hui; Yang, Ying; Zhang, Xin; Ma, Xingyu; Wang, Jie

2015-01-01

Graphical abstract: In–situ nitrogenated graphene–few layer MoS 2 composites are fabricated by combinating chemical and hydrothermal reduction. The resulting MoS 2 /N–rGO–HA by N 2 H 4 ·H 2 O and NH 3 ·H 2 O as co-reductant exhibits high activity and remarkable stability for hydrogen evolution reaction (HER). The excellent electro-catalytic performance is ascribed to the synergistic effects, confinement effects and highly dispersed MoS 2 nanosheets on N-doping rGO. Display Omitted -- Highlights: • In–situ nitrogenated graphene–few layer MoS 2 composites are fabricated by combinating chemical and hydrothermal co-reduction. • The resulting MoS 2 /N–rGO–HA exhibits high activity and remarkable stability for HER. • The excellent electro-catalytic performance is ascribed to the synergistic effects, confinement effects and highly dispersed MoS 2 nanosheets on N-doping rGO. -- Abstract: A facile one–step synthetic strategy by combinating chemical and hydrothermal reduction of graphene oxide and Mo precursor is proposed to fabricate in–situ nitrogenated graphene–few layer MoS 2 composite (MoS 2 /N–rGO–HA) for hydrogen evolution reaction (HER). The N–doping graphene nanosheets and highly dispersed MoS 2 nanosheets by ammonia and hydrozine as co–reductant have greatly promoted the N content, concentrations of pyridinic and graphitic N, the electron transport in electrodes, and assure high catalytic efficiency. The MoS 2 /N–rGO–HA composite exhibits extremely high activity in acidic solutions with a small onset potential of 100 mV and Tafel slope of 45 mV/dec, as well as a current density about 32.4 mA cm −2 at overpotential about 0.2 V. Moreover, such MoS 2 /N–rGO–HA electroncatalyst also shows an excellent stability during 1000 cycles with negligible loss of the cathodic current. This facile hydrothermal method could provide a promising strategy for the synthesis of in–situ nitrogen–doping graphene sheets and few�

Synthesis, characterization and thermal expansion studies on ThO2-SmO1.5 solid solutions

International Nuclear Information System (INIS)

Panneerselvam, G.; Antony, M.P.

2008-01-01

Full text: A highly homogeneous Th 1-x Sm x O 2 ; 0 ≤ x ≤ 0.8 solid solutions were synthesized by co-precipitation technique and the co-precipitated samples were sintered at 1473 K. Compositions of the solid solutions were characterized by standard wet-chemical analysis. X-ray diffraction measurements were performed in the sintered pellets for structural analysis, lattice parameter calculation and determination of solid solubility of SmO 1.5 in ThO 2 matrix. Bulk and theoretical densities of solid solutions were also determined. A fluorite structure was observed for ThO 2 -SmO 1.5 solid solutions with 0-55.2 mol % SmO 1.5 . Their thermal expansion coefficients were measured using high temperature X-ray diffraction technique. The mean linear thermal expansivity, αm for ThO 2 -SmO 1.5 solid solutions containing 17.9, 41.7 and 52.0 mole percent of SmO 1.5 were determined in the temperature range 298 to 2000 K for the first time. The mean linear thermal expansion coefficients for ThO 2 -SmO 1.5 solid solutions are 10.47x10 -6 K -1 , 11.16x10 -6 K -1 and 11.45x10 -6 K -1 , respectively. The percentage linear thermal expansion in this temperature range, for ThO 2 -SmO 1.5 solid solutions containing 17.9, 41.7 and 52.0 mol % SmO 1.5 are 1.82,1.94 and 1.99 respectively. It is suggested that the solid solutions are stable up to 2000 K. It is also suggested that the effect and nature of the dopant are the important parameters influenced in the thermal expansion of the ThO 2

Sm2FeTaO7 Photocatalyst for Degradation of Indigo Carmine Dye under Solar Light Irradiation

Directory of Open Access Journals (Sweden)

Leticia M. Torres-Martínez

2012-01-01

Full Text Available This paper is focused to study Sm2FeTaO7 pyrochlore-type compound as solar photocatalyst for the degradation of indigo carmine dye in aqueous solution. Sm2FeTaO7 was synthesized by using conventional solid state reaction and sol-gel method. X-ray diffraction results indicated that Sm2FeTaO7 exhibit a monoclinic crystal structure. By scanning electron microscopy analysis, it was observed that sol-gel material presents particle size of around 150 nm. The specific surface area and energy bandgap values were 12 m2 g−1 and 2.0 eV, respectively. The photocatalytic results showed that indigo carmine molecule can be degraded under solar light irradiation using the synthesized materials, sol-gel photocatalyst was 8 times more active than solid state. On the other hand, when Sm2FeTaO7 was impregnated with CuO as cocatalyst the photocatalytic activity was increased because CuO acts as electron trap decreasing electron-hole pair recombination rates.

Impact of reduced graphene oxide on MoS{sub 2} grown by sulfurization of sputtered MoO{sub 3} and Mo precursor films

Energy Technology Data Exchange (ETDEWEB)

Pacley, Shanee, E-mail: shanee.pacley@us.af.mil; Brausch, Jacob; Beck-Millerton, Emory [U.S. Air Force Research Laboratory (AFRL)/Wright Patterson Air Force Base, Wright Patterson, Ohio 45433-7707 (United States); Hu, Jianjun; Jespersen, Michael [University of Dayton Research Institute, 300 College Park, Dayton, Ohio 45469 (United States); Hilton, Al [Wyle Laboratories, 4200 Colonel Glenn Hwy, Beavercreek, Ohio 45431 (United States); Waite, Adam [University Technology Corporation, 1270 N Fairfield Rd., Beavercreek, Ohio 45432 (United States); Voevodin, Andrey A. [Department of Materials Science and Engineering, University of North Texas, 1155 Union Circle, Denton, Texas 76203 (United States)

2016-07-15

Monolayer molybdenum disulfide (MoS{sub 2}), a two dimensional semiconducting dichalcogenide material with a bandgap of 1.8–1.9 eV, has demonstrated promise for future use in field effect transistors and optoelectronics. Various approaches have been used for MoS{sub 2} processing, the most common being chemical vapor deposition. During chemical vapor deposition, precursors such as Mo, MoO{sub 3}, and MoCl{sub 5} have been used to form a vapor reaction with sulfur, resulting in thin films of MoS{sub 2}. Currently, MoO{sub 3} ribbons and powder, and MoCl{sub 5} powder have been used. However, the use of ribbons and powder makes it difficult to grow large area-continuous films. Sputtering of Mo is an approach that has demonstrated continuous MoS{sub 2} film growth. In this paper, the authors compare the structural properties of MoS{sub 2} grown by sulfurization of pulse vapor deposited MoO{sub 3} and Mo precursor films. In addition, they have studied the effects that reduced graphene oxide (rGO) has on MoS{sub 2} structure. Reports show that rGO increases MoS{sub 2} grain growth during powder vaporization. Herein, the authors report a grain size increase for MoS{sub 2} when rGO was used during sulfurization of both sputtered Mo and MoO{sub 3} precursors. In addition, our transmission electron microscopy results show a more uniform and continuous film growth for the MoS{sub 2} films produced from Mo when compared to the films produced from MoO{sub 3}. Atomic force microscopy images further confirm this uniform and continuous film growth when Mo precursor was used. Finally, x-ray photoelectron spectroscopy results show that the MoS{sub 2} films produced using both precursors were stoichiometric and had about 7–8 layers in thickness, and that there was a slight improvement in stoichiometry when rGO was used.

Highly efficient dual cocatalyst-modified TiO2 photocatalyst: RGO as electron-transfer mediator and MoSx as H2-evolution active site

Science.gov (United States)

Xu, Ying; Li, Yongan; Wang, Ping; Wang, Xuefei; Yu, Huogen

2018-02-01

The rapid interfacial charge transfer and interfacial catalytic reaction are highly desirable to improve the photocatalytic H2-evolution performance of semiconductor photocatalysts. To achieve the goal, in the paper, MoSx-rGO/TiO2 was synthesized by a facilely two-step photocatalytic reduction approach including reducing GO/TiO2 to rGO/TiO2 and then reducing ammonium tetrathiomolybdate ((NH4)2MoS4) to form amorphous MoSx on the rGO surface. In the case, the rGO nanosheets as an electron mediator caused rapid transportation of photogenerated electrons from the conduction band (CB) of TiO2, while amorphous MoSx served as an effective active site for the following interfacial reduction reaction for H2 evolution. The photocatalytic results indicated that the H2-evolution rate of synthesized MoSx-rGO/TiO2 was 206.6 μmol h-1, which was obviously higher than that of TiO2 (6.9 μmol h-1), rGO/TiO2 (31.8 μmol h-1) and MoSx/TiO2 (150.1 μmol h-1) due to the rapid interfacial charge transfer and interfacial catalytic reaction. Considering the present mild and green approach, the obtained MoSx-rGO/TiO2 could be regarded as a potential photocatalyst for the practical application. In addition, this work also could provide some new insights for the smart design and preparation of inexpensive and high-efficiency photocatalytic materials.

V sub 2 O sub 5 -based glasses as cathodes for lithium batteries

Energy Technology Data Exchange (ETDEWEB)

Levy, M; Duclot, M J; Rousseau, F [British Columbia Univ., Vancouver (Canada)

1989-05-01

The electronic conductivities of glasses in the TeO2-V2O5 and TeO2-V2O5-MoO3 systems have been determined in the 20-200 C temperature range to give simple Arrhenius relationships. Chemical and electrochemical lithium intercalations have been performed, showing that V2O5-based glasses are suitable positive electrode materials for lithium batteries. 20 refs.

Structural and spectral properties of MgZnO2:Sm3+ phosphor

Science.gov (United States)

Rajput, Preasha; Sharma, Pallavi; Biswas, Pankaj; Kamni

2018-05-01

The samarium doped MgZnO2 phosphor was synthesized by the low-cost combustion method. The powder X-ray diffraction (XRD) analysis confirmed the crystallinity and phase purity of the phosphor. The lattice parameters were determined by indexing the diffraction peaks. The photoluminescence (PL) study revealed that the phosphor exhibited a broad excitation band in the UV region ranging between 200 to 350 nm. The 601 nm emission was ascribed to 4G5/2 to 6H7/2 transitions of the Sm3+ ion. The optical bandgap of MgZnO2:Sm3+ was obtained to be 3.56 eV. The phosphor can be projected as a useful material in X- and gamma-ray scintillators.

EPR study of the coordination sphere of Mo5+ ions in UV-irradiated silica-supported molybdenum catalysts

International Nuclear Information System (INIS)

Canose, B.; Gonzalez-Elipe, A.R.; Che, M.

1991-01-01

The determination of the number of coordination vacancies existing at transition metal cations at the surface of bulk or supported oxides is of greater interest in relation to the adsorption and catalytic properties of such systems. In the case of paramagnetic cations, the authors have developed a method consisting of the recording of their first and third derivative EPR spectra after adsorption of 13 CO, ( 13 C, I = 1/2). In this way, the 13 C superhyperfine structure which is normally observed permits the determination of the number of CO molecules bonded to the metal center. In a recent EPR work published in this journal, Seyedmonir and Howe have reported the formation of a CO adduct of the tetrahedral Mo 5+ -OH - species formed by UV-irradiation at 20 K of a MoO 3 /SiO 2 catalyst in the presence of H 2 . In that work, although the structure of such an adduct could not be derived unambiguously on the basis of the g tensor values, the coordination of the Mo 5+ ion by two CO molecules was suggested. This would be in agreement with the previous results with thermally reduced V 2 O 5 /SiO 2 and MoO 3 /SiO 2 catalysts, where the coordination of, respectively, V 4+ and Mo 5+ tetrahedral centers by two CO molecules was proven by means of the combined use of 13 CO and third derivative EPR spectra. In the present work, using this approach, they have studied the structure of these Mo 5+ ions photochemically generated on MoO 3 /SiO 2 catalysts and concluded that only one CO molecule is bonded to the paramagnetic ion

Synthesis, Characterization and Catalytic Activity of Cu/Cu2O Nanoparticles Prepared in Aqueous Medium

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Sayed M. Badawy

2015-07-01

Full Text Available Copper/Copper oxide (Cu/Cu2O nanoparticles were synthesized by modified chemical reduction method in an aqueous medium using hydrazine as reducing agent and copper sulfate pentahydrate as precursor. The Cu/Cu2O nanoparticles were characterized by X-ray Diffraction (XRD, Energy Dispersive X-ray Fluorescence (EDXRF, Scanning Electron Microscope (SEM, and Transmission Electron Microscope (TEM. The analysis revealed the pattern of face-centered cubic (fcc crystal structure of copper Cu metal and cubic cuprites structure for Cu2O. The SEM result showed monodispersed and agglomerated particles with two micron sizes of about 180 nm and 800 nm, respectively. The TEM result showed few single crystal particles of face-centered cubic structures with average particle size about 11-14 nm. The catalytic activity of Cu/Cu2O nanoparticles for the decomposition of hydrogen peroxide was investigated and compared with manganese oxide MnO2. The results showed that the second-order equation provides the best correlation for the catalytic decomposition of H2O2 on Cu/Cu2O. The catalytic activity of hydrogen peroxide by Cu/Cu2O is less than the catalytic activity of MnO2 due to the presence of copper metal Cu with cuprous oxide Cu2O. © 2015 BCREC UNDIP. All rights reservedReceived: 6th January 2015; Revised: 14th March 2015; Accepted: 15th March 2015How to Cite: Badawy, S.M., El-Khashab, R.A., Nayl, A.A. (2015. Synthesis, Characterization and Catalytic Activity of Cu/Cu2O Nanoparticles Prepared in Aqueous Medium. Bulletin of Chemical Reaction Engineering & Catalysis, 10 (2: 169-174. (doi:10.9767/bcrec.10.2.7984.169-174 Permalink/DOI: http://dx.doi.org/10.9767/bcrec.10.2.7984.169-174  

Double hollow MoS{sub 2} nano-spheres: Synthesis, tribological properties, and functional conversion from lubrication to photocatalysis

Energy Technology Data Exchange (ETDEWEB)

Liu, Yueru [Department of Chemical and Materials Engineering, Hefei University, Hefei 230601 (China); Hu, Kunhong, E-mail: hukunhong@163.com [Department of Chemical and Materials Engineering, Hefei University, Hefei 230601 (China); Hu, Enzhu; Guo, Jianhua; Han, Chengliang [Department of Chemical and Materials Engineering, Hefei University, Hefei 230601 (China); Hu, Xianguo [Institute of Tribology, Hefei University of Technology, Hefei 230009 (China)

2017-01-15

Highlights: • Novel double-hollow-sphere MoS{sub 2} nanoparticles were synthesized on sericite. • Friction and wear decreased by 22.4 and 63.5% by the novel MoS{sub 2}/sericite. • Friction induced conversion of MoS{sub 2}/sericite from lubricant to catalyst. • MoS{sub 2}/sericite can be used as a photocatalyst after lubricating service life. • A possible approach was proposed for designing a novel green lubricant. - Abstract: Molybdenum disulfide (MoS{sub 2}) has extensive applications in industries as solid lubricants and catalysts. To improve the lubricating performance of MoS{sub 2}, novel double-hollow-sphere MoS{sub 2} (DHSM) nanoparticles with an average diameter of approximately 90 nm were synthesized on sericite mica (SM). When the DHSM/SM composite was used as an additive in polyalphaolefin oil, friction and wear decreased by 22.4% and 63.5% respectively. The low friction and wear were attributed to the easy exfoliation of DHSM. The DHSM/SM composite was then rubbed under 40 MPa for 1 h to investigate the exfoliation and functional conversion behaviors of DHSM. Results showed that DHSM (lubricating structure) on SM could be completely exfoliated into nanosheets (catalytic structure) by rubbing. The nanosheets exfoliated from DHSM presented good photocatalytic activity for the removal of organic compounds from waste water. This work provided both a novel solid lubricant for industrial applications and a possible approach to designing a novel green lubricant for use as a photocatalyst in organic-waste treatment after lubricating service life.

Synthesis by two methods and crystal structure determination of a new pyrochlore-related compound Sm{sub 2}FeTaO{sub 7}

Energy Technology Data Exchange (ETDEWEB)

Torres-Martinez, Leticia M., E-mail: lettorresg@yahoo.com [Departamento de Ecomateriales y Energia, Facultad de Ingenieria Civil, Universidad Autonoma de Nuevo Leon, Cd. Universitaria, San Nicolas de los Garza, Nuevo Leon 66450 (Mexico); Ruiz-Gomez, Miguel A. [Departamento de Ecomateriales y Energia, Facultad de Ingenieria Civil, Universidad Autonoma de Nuevo Leon, Cd. Universitaria, San Nicolas de los Garza, Nuevo Leon 66450 (Mexico); Facultad de Ciencias Quimicas, Universidad Autonoma de San Luis Potosi, Av. Manuel Nava 6, San Luis Potosi, S.L.P. 78290 (Mexico); Figueroa-Torres, M.Z.; Juarez-Ramirez, Isaias [Departamento de Ecomateriales y Energia, Facultad de Ingenieria Civil, Universidad Autonoma de Nuevo Leon, Cd. Universitaria, San Nicolas de los Garza, Nuevo Leon 66450 (Mexico); Moctezuma, Edgar [Facultad de Ciencias Quimicas, Universidad Autonoma de San Luis Potosi, Av. Manuel Nava 6, San Luis Potosi, S.L.P. 78290 (Mexico); and others

2012-04-16

Graphical abstract: The monoclinic (space group C2/c) structure of a new compound, Sm{sub 2}FeTaO{sub 7} shows an alternating Sm-O and Fe/Ta-O layers. In the Fe/Ta-O layer, Fe/Ta1 and Fe/Ta3 cations are coordinated by six oxygen atoms, forming irregular octahedral interconnected into a hexagonal tungsten bronze (HTB) type network. The HTB layer is a fundamental framework in the pyrohlore-related structure. Highlights: Black-Right-Pointing-Pointer Pyrochlore-related compound Sm{sub 2}FeTaO{sub 7} prepared by solid state reaction and sol-gel. Black-Right-Pointing-Pointer Sm{sub 2}FeTaO{sub 7} crystallizes with a monoclinic crystal structure and space group C2/c. Black-Right-Pointing-Pointer The compound is synthesized by sol-gel at lower temperature and time than solid state. Black-Right-Pointing-Pointer Surface area of sol-gel Sm{sub 2}FeTaO{sub 7} is 10 times higher than that prepared by solid state. - Abstract: This paper reports on the synthesis of a new pyrochlore-related compound Sm{sub 2}FeTaO{sub 7} by both solid state reaction and sol-gel synthesis routes. Structural features were determined by X-ray powder diffraction and Rietveld refinement and were corroborated using Transmission Electron Microscopy (TEM). The results revealed that Sm{sub 2}FeTaO{sub 7} crystallized in the monoclinic system with space group C2/c and the following cell parameters: a = 13.1307(5) Angstrom-Sign , b = 7.5854(3) Angstrom-Sign , c = 11.6425(4) Angstrom-Sign and {beta} = 100.971(2) Degree-Sign . The monoclinic structure of Sm{sub 2}FeTaO{sub 7} showed an arrangement of alternating Sm-O and Fe/Ta-O layers and two types of irregular octahedra of Fe/Ta-O, which are interconnected into a hexagonal tungsten bronze (HTB)-type network. On the other hand, Sm{sub 2}FeTaO{sub 7} prepared by sol-gel was obtained with lower particle sizes than the solid state produced compound. The difference in particle size causes a difference of one order of magnitude in the specific surface area. In

Activating basal-plane catalytic activity of two-dimensional MoS2 monolayer with remote hydrogen plasma

KAUST Repository

Cheng, Chia-Chin; Lu, Ang-Yu; Tseng, Chien-Chih; Yang, Xiulin; Hedhili, Mohamed N.; Chen, Min-Cheng; Wei, Kung-Hwa; Li, Lain-Jong

2016-01-01

that account for a small percentage of the surface area, rather than the basal planes, of MoS2 monolayer have been confirmed as their active catalytic sites. As a result, extensive efforts have been developing in activating the basal planes of MoS2

The lanthanum(III molybdate(VI La4Mo7O27

Directory of Open Access Journals (Sweden)

Petra Becker

2009-08-01

Full Text Available Crystals of the orthorhombic phase La4Mo7O27 (lanthanum molybdenum oxide were obtained from a non-stoichiometric melt in the pseudo-ternary system La2O3–MoO3–B2O3. In the crystal structure, distorted square-antiprismatic [LaO8] and monocapped square-antiprismatic [LaO9] polyhedra are connected via common edges and faces into chains along [010]. These chains are arranged in layers that alternate with layers of [MoO4] and [MoO5] polyhedra parallel to (001. In the molybdate layers, a distorted [MoO5] trigonal bipyramid is axially connected to two [MoO4] tetrahedra, forming a [Mo3O11] unit.

Crystal growth of Sm0.3Tb0.7FeO3 and spin reorientation transition in Sm1−xTbxFeO3 orthoferrite

International Nuclear Information System (INIS)

Wu, Anhua; Wang, Bo; Zhao, Xiangyang; Xie, Tao; Man, Peiwen; Su, Liangbi; Kalashnikova, A.M.; Pisarev, R.V.

2017-01-01

In this work, Sm 0.3 Tb 0.7 FeO 3 single crystal was successfully grown by optical floating zone method. Sm 0.3 Tb 0.7 FeO 3 samples with a-, b-, and c-orientation were manufactured by means of Laue photograph. Magnetic properties of Sm 0.3 Tb 0.7 FeO 3 single crystals are studied over a wide temperature range from 2 to 400 K. Spin reorientation transition from Γ 2 to Γ 4 are observed by means of the temperature dependence of magnetization It indicated the reorientation transition temperature of Sm 1−x Tb x FeO 3 single crystals is lowered with the contents of Tb contents rising based on this work and our previous works, thus the spin reorientation transition temperature can be adjusted through changing the compound in orthoferrites materials, which means that we can get orthoferrites single crystals with high magnetism property in various temperature through material design. - Highlights: • Sm 0.3 Tb 0.7 FeO 3 single crystals with various compounds were successfully grown by optical floating zone method. • The relation between SRT temperature and composition in Sm 1−x Tb x FeO 3 orthoferrite was indicated. • The spin reorientation transition temperature of Sm 1−x Tb x FeO 3 single crystals can be adjusted through changing the compound in orthoferrites materials.

Explorations of new phases in the Ga(III)/In(III)-Mo(VI)-Se(IV)/Te(IV)-O systems.

Science.gov (United States)

Kong, Fang; Hu, Chun-Li; Hu, Ting; Zhou, Yong; Mao, Jiang-Gao

2009-07-07

Systematic explorations of new phases in the Ga(III)/In(III)-Mo(VI)-Se(IV)/Te(IV)-O systems by hydrothermal syntheses or solid-state reactions at high-temperature led to four new quaternary compounds, namely, Ga(2)MoQ(2)O(10) (Q = Se, Te), In(2)Mo(2)Se(2)O(13)(H(2)O) and In(2)MoTe(2)O(10). Ga(2)MoQ(2)O(10) (Q = Se, Te) are isostructural and their structures feature a 3D network of gallium selenite/tellurite with 12-member ring tunnels along b-axis, the distorted MoO(6) octahedra are attached on the wall of the above tunnels. The structure of In(2)Mo(2)Se(2)O(13)(H(2)O) features a new pillared-layered architecture composed of 2D indium(III) selenite layers that are interconnected by Mo(2)O(10) dimers, forming 8-membered ring tunnels along the b-axis. The structure of In(2)MoTe(2)O(10) features a 2D indium oxide layer formed by corner- and edge-sharing InO(6) and InO(7) polyhedra with MoO(4) tetrahedra and TeO(n) (n = 4, 5) polyhedra hanging on both sides of the layer, there are weak interlayer Te-O bonds of 2.512 A. Results of optical diffuse reflectance spectrum measurements indicate that all four compounds are insulators, which are in agreement with results of band structure calculations based on DFT methods.

Influence of phase composition and structure of V-Mo mixed catalysts on the activity and selectivity in the oxidation of benzene to maleic anhydride

International Nuclear Information System (INIS)

Kripylo, P.; Ritter, D.; Hahn, H.; Spiess, H.; Kraak, P.

1981-01-01

Whereas MoO 3 and phosphate stabilize the low valence states of vanadium in the phase structure of V-Mo mixed catalysts, CoO influences the activity only, but not the selectivity. The catalysts show maxima of activity and selectivity at V/Mo ratios of 4 to 6. Ageing is caused by phase separation connected with the appearance of an MoO 3 phase and an increase of the V/Mo ratio in the phase of the active component

A Temperature Window for the Synthesis of Single-Walled Carbon Nanotubes by Catalytic Chemical Vapor Deposition of CH4over Mo2-Fe10/MgO Catalyst

Directory of Open Access Journals (Sweden)

Yu Ouyang

2009-01-01

Full Text Available Abstract A temperature window for the synthesis of single-walled carbon nanotubes by catalytic chemical vapor deposition of CH4over Mo2-Fe10/MgO catalyst has been studied by Raman spectroscopy. The results showed that when the temperature is lower than 750 °C, there were few SWCNTs formed, and when the temperature is higher than 950 °C, mass amorphous carbons were formed in the SWCNTs bundles due to the self-decomposition of CH4. The temperature window of SWCNTs efficient growth is between 800 and 950 °C, and the optimum growth temperature is about 900 °C. These results were supported by transmission electron microscope images of samples formed under different temperatures. The temperature window is important for large-scale production of SWCNTs by catalytic chemical vapor deposition method.

Hydrogen Doping into MoO3 Supports toward Modulated Metal-Support Interactions and Efficient Furfural Hydrogenation on Iridium Nanocatalysts.

Science.gov (United States)

Xie, Lifang; Chen, Ting; Chan, Hang Cheong; Shu, Yijin; Gao, Qingsheng

2018-03-16

As promising supports, reducible metal oxides afford strong metal-support interactions to achieve efficient catalysis, which relies on their band states and surface stoichiometry. In this study, in situ and controlled hydrogen doping (H doping) by means of H 2 spillover was employed to engineer the metal-support interactions in hydrogenated MoO x -supported Ir (Ir/H-MoO x ) catalysts and thus promote furfural hydrogenation to furfuryl alcohol. By easily varying the reduction temperature, the resulting H doping in a controlled manner tailors low-valence Mo species (Mo 5+ and Mo 4+ ) on H-MoO x supports, thereby promoting charge redistribution on Ir and H-MoO x interfaces. This further leads to clear differences in H 2 chemisorption on Ir, which illustrates its potential for catalytic hydrogenation. As expected, the optimal Ir/H-MoO x with controlled H doping afforded high activity (turnover frequency: 4.62 min -1 ) and selectivity (>99 %) in furfural hydrogenation under mild conditions (T=30 °C, PH2 =2 MPa), which means it performs among the best of current catalysts. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Preparation and Characterization of NiMo/Al2O3Catalyst for Hydrocracking Processing

Directory of Open Access Journals (Sweden)

Widiyadi Aditya

2018-01-01

Full Text Available Hydrocracking is a chemical process used in petroleum refineries for converting high boiling hydrocarbons in petroleum crude oils to more valuable lower boiling products such as gasoline, kerosene, and diesel oil that operate at high temperature and pressure. Catalyst was used in hydrocracking to reduce temperature and pressure. Hydrocracking catalyst are composed of active components and support. Alumina is widely used in hydrocracking process as catalyst support due to its high surface area, high thermal stability, and low prices. The objective of this research was preparated NiMo/Al2O3 catalyst that used as hydrocracking catalyst. Catalyst was synthesized by wetness impregnation method and simple heating method with various kind of Al2O3. The physicochemical properties of catalyst were investigated by X-ray diffraction (XRD to determine type of crystal and scanning electron microscopy (SEM to determine morphology of the catalyst. The NiMo/Al2O3 catalyst prepared by aluminium potassium sulfate dodecahydrate exhibited the highest crystallinity of 90.23% and it is clear that MoO3 and NiO crystallites are highly dispersed on the NiMo/Al2O3 catalyst which indicates as the best catalyst. The catalytic activity in hydrocracking process was successfully examined to convert fatty acid into hydrocarbon.

Preparation and Characterization of NiMo/Al2O3Catalyst for Hydrocracking Processing

Science.gov (United States)

Widiyadi, Aditya; Guspiani, Gema Adil; Riady, Jeffry; Andreanto, Rikky; Chaiunnisa, Safina Dea; Widayat

2018-02-01

Hydrocracking is a chemical process used in petroleum refineries for converting high boiling hydrocarbons in petroleum crude oils to more valuable lower boiling products such as gasoline, kerosene, and diesel oil that operate at high temperature and pressure. Catalyst was used in hydrocracking to reduce temperature and pressure. Hydrocracking catalyst are composed of active components and support. Alumina is widely used in hydrocracking process as catalyst support due to its high surface area, high thermal stability, and low prices. The objective of this research was preparated NiMo/Al2O3 catalyst that used as hydrocracking catalyst. Catalyst was synthesized by wetness impregnation method and simple heating method with various kind of Al2O3. The physicochemical properties of catalyst were investigated by X-ray diffraction (XRD) to determine type of crystal and scanning electron microscopy (SEM) to determine morphology of the catalyst. The NiMo/Al2O3 catalyst prepared by aluminium potassium sulfate dodecahydrate exhibited the highest crystallinity of 90.23% and it is clear that MoO3 and NiO crystallites are highly dispersed on the NiMo/Al2O3 catalyst which indicates as the best catalyst. The catalytic activity in hydrocracking process was successfully examined to convert fatty acid into hydrocarbon.

Half-metallic behavior and electronic structure of Sr2CrMoO6 magnetic system

International Nuclear Information System (INIS)

Bonilla, C.M.; Landinez Tellez, D.A.; Arbey Rodriguez, J.; Vera Lopez, E.; Roa-Rojas, J.

2007-01-01

Complex perovskite materials with the A 2 BB'O 6 formula have been recently studied because of their peculiar magnetic and electronic properties. The origin of magnetism in the double perovskite Sr 2 FeMoO 6 brought these properties again into discussion. Recently, a new interaction mechanism was proposed for cases in which the hybridization of 3d and 2p levels of Mo with the 3d Fe levels is responsible for the half-metallic behavior in the Sr 2 FeMoO 6 material. We report on LAPW ab initio calculations within the generalized gradient approximation (GGA) to density functional theory (DFT) for another double perovskite, namely, Sr 2 CrMoO 6 . Our results show that this is also a half-metallic system. We correlate our results with an extension of the recent model proposed by Sarma to explain the conduction mechanism in this compound

Fluorometric determination of vanadium (V) by utilizing its catalytic effect on the oxidation of o-aminophenol by chlorate

Energy Technology Data Exchange (ETDEWEB)

Hiraki, K; Shimizu, N; Nishikawa, Y [Kinki Univ., Higashi-Osaka, Osaka (Japan). Faculty of Science and Technology; Shigematsu, T

1981-12-01

The oxidation of o-aminophenol by chlorate ion takes place in acidic milieu and is catalyzed by a trace amount of vanadium (V). Vanadium (V) oxidizes o-aminophenol to 2-amino-3-phenoxazone, then the vanadium (IV) produced is reoxidized to vanadium (V) by the sodium chlorate. Further oxidation of o-aminophenol proceeds by repetition of these reactions. The oxidation product (2-amino-3-phenoxazone) gives an intense fluorescence; under optimum conditions, the fluorescence intensity is proportional to the concentration of vanadium. The most suitable concentration of o-aminophenol and sodium chlorate for the determination of vanadium (V) were found to be 0.02 M and 2 x 10/sup -4/ M, respectively. From 0.1 ppm to 5 ppm of vanadium (V) can be determined under the optimum conditions; reaction temperature 50/sup 0/C, reaction time 2 h, and at pH 2 +- 0.2. If the reaction time is increased to 3 h at 55/sup 0/C, the method may be extended from 2 ppb to 15 ppb of vanadium. Interferences of diverse ions were tested, among which Fe (III) and Mn (VII) caused positive errors, and Cr (VI), Mo (VI) negative errors if present in 40 fold w/w ratio to V (V).

The application of Cu/SiO2 catalytic system in chemical mechanical planarization based on the stability of SiO2 sol

International Nuclear Information System (INIS)

Li Yan; Liu Yuling; Wang Aochen; Yang Zhixin; Sun Mingbin; Cheng Chuan; Zhang Yufeng; Zhang Nannan

2014-01-01

There is a lot of hydroxyl on the surface of nano SiO 2 sol used as an abrasive in the chemical mechanical planarization (CMP) process, and the chemical reaction activity of the hydroxyl is very strong due to the nano effect. In addition to providing a mechanical polishing effect, SiO 2 sol is also directly involved in the chemical reaction. The stability of SiO 2 sol was characterized through particle size distribution, zeta potential, viscosity, surface charge and other parameters in order to ensure that the chemical reaction rate in the CMP process, and the surface state of the copper film after CMP was not affected by the SiO 2 sol. Polarization curves and corrosion potential of different concentrations of SiO 2 sol showed that trace SiO 2 sol can effectively weaken the passivation film thickness. In other words, SiO 2 sol accelerated the decomposition rate of passive film. It was confirmed that the SiO 2 sol as reactant had been involved in the CMP process of copper film as reactant by the effect of trace SiO 2 sol on the removal rate of copper film in the CMP process under different conditions. In the CMP process, a small amount of SiO 2 sol can drastically alter the chemical reaction rate of the copper film, therefore, the possibility that Cu/SiO 2 as a catalytic system catalytically accelerated the chemical reaction in the CMP process was proposed. According to the van't Hoff isotherm formula and the characteristics of a catalyst which only changes the chemical reaction rate with out changing the total reaction standard Gibbs free energy, factors affecting the Cu/SiO 2 catalytic reaction were derived from the decomposition rate of Cu (OH) 2 and the pH value of the system, and then it was concluded that the CuSiO 3 as intermediates of Cu/SiO 2 catalytic reaction accelerated the chemical reaction rate in the CMP process. It was confirmed that the Cu/SiO 2 catalytic system generated the intermediate of the catalytic reaction (CuSiO 3 ) in the CMP process

Morphology-dependent electrocatalytic performance of Fe2(MoO43 for electro-oxidation of methanol in alkaline medium

Directory of Open Access Journals (Sweden)

Daoming Zhang

2017-06-01

Full Text Available Electrochemically synthesized nanosphere, nanorod and nanotube Fe2(MoO43 at optimized temperature and current density are characterized with XRD, SEM, TEM, XPS. Crystal lattices of the three types Fe2(MoO43 detected by HRTEM are well matched with the simulation analysis results from Materials Studio 6.0 based on the inorganic crystal structure database (ICSD data and the modified XRD lattice parameters. The ratios of Fe/Mo on the surface resulted from XPS analysis are 1.47, 1.63 and 2.22 respectively for nanosphere, nanorod and nanotube. The mixture of Fe2(MoO43 with polytetrafluoroethylene dispersion are coated on glass carbon substrate as electrode for electrocatalytic performance test by cyclic voltammetries in 0.1 mol/L KOH and 1 mol/L methanol electrolyte. Methanol oxidation peak current density of the Nanotube- Fe2(MoO43/GCEs electrode is 3.27 mA/cm2 higher than 2.8 mA/cm2 of platinum foil electrode, which shows enhanced catalytic activity of Nanotube-Fe2(MoO43/GCEs. The cyclic stability in terms of peak current retention are 91%, 92% and 88% respectively for Nanosphere-Fe2(MoO43/GCE, Nanorod-Fe2(MoO43/GCE and Nanotube-Fe2(MoO43/GCE electrode after 220 cycles. It is concluded that nanosized Fe2(MoO43 could be promising alternative non-noble electro-catalysts for electro-oxidation of methanol in alkaline medium.

Study of the effect of different mixed supports on the catalytic activity and the structure of Bi2MoxW1-xO6 catalysts

International Nuclear Information System (INIS)

Rangel, R.; Cervantes L, J. L.; Espino, J.; Nunez G, R.; Bartolo P, P.; Gomez C, A.; Diaz, G.

2014-01-01

A series of Bi 2 Mo x W 1-x O 6 catalysts supported on Al 2 O 3 -SiO 2 , SiO 2 -TiO 2 and activated carbon were synthesized. The aim was to compare the different supports and calcination temperature of catalysts, studying their efficiency and activation temperature in the CO oxidation reaction. The catalysts active phase, Bi 2 Mo x W 1-x O 6 was made by means of chemical precipitation procedure starting from high purity (NH 4 ) 6 Mo 7 O 24 ·4H 2 O, (NH 4 ) 6 W 12 O 6 ·H 2 O, Bi(NO 3 ) 2 ·5H 2 O compounds, which afterwards, were supported on Al 2 O 3 -SiO 2 , SiO 2 -TiO 2 and activated carbon through impregnation. The catalysts characterization was carried out by means of X-ray diffraction analysis, scanning electron microscopy and surface area determination (Bet method). Regarding the catalytic activity the Bi 2 Mo x W 1-x O 6 /carbon activated compound synthesized at 500 grades C was the best catalyst being activated at 125 grades C reaching 90% conversion. It is concludes that was observed an effect of calcination temperature and the support on the different values reached for the catalytic activity. (Author)

Geochemical behaviour of U3O8, Mo, Y, Ga, V and Zr in laterite - bauxitic sequence of the ''Croanta-Paragominas''

International Nuclear Information System (INIS)

Ferraioli, R.N.M.; Ferreira, Z.C.A.

1987-10-01

Fifteen samples are studied, analyzed for U 3 O 8 (delayed neutrons), ThO 2 (X-ray fluorescence spectrometry) and Mo, Y, Ga, V and Zr (optical emission spectrography) in laterite - bauxitic sequence of the Paragominas, Brazil. Generical datas about the arrangements of thorium, uranium and zirconium are also presented. (C.G.C.) [pt

Structure of β-TlMo2P3O13

International Nuclear Information System (INIS)

Costentin, G.; Borel, M.M.; Grandin, A.; Leclaire, A.; Raveau, B.

1991-01-01

Thallium molybdenum triphosphate, TlMo 2 P 3 O 13 , M r =679.16, monoclinic, P2 1 /c, a=9.7536 (3), b=19.0640 (16), c=6.3945 (7) A, β=107.099 (7) 0 , V=1136 (2) A 3 , Z=4, D m not measured, D x =4.08 Mg m -3 , λ(MoKα)=0.71073 A, μ=16.90 mm -1 , F(000)=314, T=293 K, 951 reflections, R=0.047, ωR=0.047. The lattice is built up from MoO 6 , PO 4 and P 2 O 7 groups delimiting tunnels where the Tl + ions are located. The title compound is isotyopic with β-KMo 2 P 3 O 13 . (orig.)

Preparation of NO-doped β-MoO{sub 3} and its methanol oxidation property

Energy Technology Data Exchange (ETDEWEB)

Pham, Thi Thuy Phuong, E-mail: pttphuong@ict.vast.vn; Nguyen, Phuc Hoang Duy; Vo, Tan Tai; Luu, Cam Loc; Nguyen, Huu Huy Phuc

2016-12-01

The major drawback of the industrial iron molybdate catalysts which is their deactivation problem has driven the study of alternative catalysts for formaldehyde production from methanol. In this paper, NO-doped β-MoO{sub 3} was successfully synthesized from the commercial molybdic acid powder (H{sub 2}MoO{sub 4}) and characterized by differential thermal analysis (DTA), X-ray Diffraction (XRD), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). Results obtained from XRD and Raman spectroscopy indicated that the synthesized sample has all features of the well-known β-MoO{sub 3} except for the presence of a new small peak. The curve-fitting of XPS spectra revealed that nitrogen-containing species may be present in the form of negatively charged nitrogen oxide in the prepared sample. Due to its metastable nature, NO-doped β-MoO{sub 3} may be transformed into the thermally stable α-MoO{sub 3} at temperature higher than 400 °C as pointed out by DTA study. However, when the reaction temperature was as low as 300 °C, the catalyst was stable for partial methanol oxidation with no significant change in activity during 30 h of catalytic study. Methanol conversion and formaldehyde selectivity were maintained at about 98% and 99%, respectively. - Highlights: • NO-doped β-MoO{sub 3} was synthesized by a facile and effective method. • Its structure was confirmed by XRD, Raman and XPS analysis. • X{sub MeOH} and S{sub HCHO} were stabilized at 98% and 99%, respectively, for the first 30 h.

MoO{sub 3} incorporation in magnesium aluminosilicate glasses

Energy Technology Data Exchange (ETDEWEB)

Tan, Shengheng; Ojovan, Michael I.; Hyatt, Neil C.; Hand, Russell J.

2015-03-15

Molybdate has a very low solubility in silicate and borosilicate glass systems and its excess presence in nuclear waste glass can cause the formation of a readily soluble “yellow phase”. In this study, the incorporation of molybdenum oxide (MoO{sub 3}) in a magnesium aluminosilicate glass system has been investigated. The prepared glasses show a higher than 90% molybdenum retention rate and up to 5.34 mol% (12.28 wt%) MoO{sub 3} can be incorporated into these glasses without causing visible phase separation. The incorporation of MoO{sub 3} increases glass density, decreases glass transition and crystallisation temperatures and intensifies Raman bands assigned to vibrations of MoO{sub 4}{sup 2−} units. When excess molybdate is added liquid–liquid phase separation and crystallisation occurs. The separated phase is spherical, 200–400 nm in diameter and randomly dispersed. Based on powder X-ray diffraction, Raman spectroscopy and transmission electron microscopy, the separated phase is identified as MgMoO{sub 4}.

On the coexistence of copper-molybdenum bronzes: CuxMoO₃ (0.2 < x < 0.25; typically x = 0.23) and CuyMoO_3-z (0.1 < y < 0.2; typically y = 0.15) in the Cu-MoO₂-O quasi-ternary system

DEFF Research Database (Denmark)

Warner, Terence Edwin; Skou, Eivind Morten

2010-01-01

Two copper-molybdenum bronzes: CuyMoO3-z (0.1black polycrystalline materials by the solid state reaction of Cu and MoO3 at 600 C under argon in Pt crucibles. Powder XRD showed that the material...... with global composition ‘0.1Cu.MoO3’ comprises ~Cu0.15MoO3 and MoO3; whilst ‘0.2Cu.MoO3’ comprises ~Cu0.15MoO3 and ~Cu0.23MoO3. DTA performed on ‘0.2Cu.MoO3’ reveals a reversible solid state phase transition = 520 C under argon. Reacting equimolar amounts of Cu2O and MoO2 at 600 C in a Cu crucible under argon...

Spray pyrolytic deposition of α-MoO3 film and its use in dye-sensitized solar cell

Science.gov (United States)

Tamboli, Parvin S.; Jagtap, Chaitali V.; Kadam, Vishal S.; Ingle, Ravi V.; Vhatkar, Rajiv S.; Mahajan, Smita S.; Pathan, Habib M.

2018-04-01

Thermal decomposition of ammonium para molybdate tetrahydrate precursor has been studied to determine degradation temperatures in air atmosphere. Current work explores the synthesis of α-MoO3 films by an economical spray pyrolysis technique using ammonium para molybdate tetrahydrate precursor in the presence of compressed air. A variety of characterization techniques such as X-ray diffraction, scanning electron microscopy, transmission electron microscopy, UV-visible spectroscopy, Fourier transform infrared, and Raman spectroscopy were carried out, and the studies have confirmed that orthorhombic phase formation of MoO3 takes place with spongy mesh-type structure. The study of electro-catalytic activity of α-MoO3 in titania-based dye-sensitized solar cell is also carried out by cyclic voltammetry, electrochemical impedance spectroscopy, and Tafel curves to evaluate its performance as a counter electrode.

MoSe2 modified TiO2 nanotube arrays with superior photoelectrochemical performance

Science.gov (United States)

Zhang, Yaping; Zhu, Haifeng; Yu, Lianqing; He, Jiandong; Huang, Chengxing

2018-04-01

TiO2 nanotube arrays (TNTs) are first prepared by anodization Ti foils in ethylene glycol electrolyte. Then, MoSe2 deposites electrochemically on TNTs. The as-synthesized MoSe2/TiO2 composite has a much higher photocurrent density of 1.07 mA cm‑2 at 0 V than pure TNTs of 0.38 mA cm‑2, which suggests that the MoSe2/TiO2 composite film has optimum photoelectrocatalysis properties. The electron transport resistances of the MoSe2/TiO2 decreases to half of pure TiO2, at 295.6 ohm/cm2. Both photocurrent-time and Mott-Schottky plots indicate MoSe2 a p-type semiconductor characteristics. MoSe2/TiO2 composite can achieve a maximum 5 orders of magnitude enhancement in carrier density (4.650 × 1027 cm‑3) than that of pure TiO2 arrays. It can be attributed to p-n heterojunction formed between MoSe2 and TiO2, and the composite can be potentially applied in photoelectrochemical, photocatalysis fields.

Determination and modeling for the solubility of Na_2WO_4·2H_2O and Na_2MoO_4·2H_2O in the (Na"+ + MoO_4"2"− + WO_4"2"− + SO_4"2"− + H_2O) system

International Nuclear Information System (INIS)

Ning, Pengge; Xu, Weifeng; Cao, Hongbin; Xu, Hongbin

2016-01-01

Highlights: • The solubility of Na_2MoO_4·2H_2O and Na_2WO_4·2H_2O in Na_2MoO_4–Na_2WO_4–Na_2SO_4–H_2O were performed. • The solubility of sodium tungstate dihydrate in Na_2WO_4–Na_2SO_4–H_2O was determined. • The new model was established via regressing the published and the determined data. • The Pitzer parameter and the solubility product constant of the salt in solution were calculated. • The model was used to estimate the solubility of the sodium molybdate and sodium tungstate. - Abstract: The solubility of sodium tungstate dihydrate and sodium molybdate dihydrate in the (Na_2MoO_4 + Na_2WO_4 + Na_2SO_4 + H_2O) system was studied using experimental and calculated methods. The osmotic coefficient of sodium tungstate was fitted to calculate the thermodynamics parameters of (Na_2WO_4 + H_2O) system. The solubility of sodium tungstate dihydrate was determined using the dynamic method in Na_2WO_4–Na_2SO_4–H_2O to establish the new model which can provide an estimate the solubility of sodium tungstate dihydrate in various conditions, combined with the data published, the solubility of sodium tungstate dihydrate and the sodium molybdate dihydrate in quaternary system of (Na_2MoO_4 + Na_2WO_4 + Na_2SO_4 + H_2O) was estimated using the parameters of the two ternary systems of (Na_2WO_4 + Na_2SO_4 + H_2O) and (Na_2MoO_4 + Na_2SO_4 + H_2O). The results show that the AARD is always small and the calculated value is basically consistent with the experimental values for the system studied.

Molybdenum x-ray absorption studies of the mutant Kp nifV of nitrogenase MO-FE protein

International Nuclear Information System (INIS)

Eidsness, M.K.; Smith, B.E.; Flood, A.C.; Garner, C.D.; Cramer, S.P.

1985-01-01

The nifV mutant nitrogenase enzyme of Klebsiella pheumoniae exhibits altered substrate reducing activity. This nitrogenase mutant cannot fix N 2 in vivo but can reduce C 2 H 2 to C 2 H 4 . The nifV mutant enzyme differs further from the wild-type enzyme by CO inhibition of its H 2 evolution activity, up to 80%. The NifV - phenotype (NifV - Kp1) has been shown to be associated with the iron-molybdenum cofactor (FeMoco) in the Mo Fe protein which is generally accepted as the site for substrate reduction. An X-Ray absorption study of the Mo site in this mutant may reveal a difference in its FeMoco structure. The authors report here a comparison of Mo X-Ray absorption data from the nitrogenase enzymes of the wild-type and NifV - strains in three different forms: (1) as isolated, (2) dye-oxidized, and (3) fixing enzyme systems. Mo edge structure of NifV - Kp1 and wild-type enzymes are nearly identical. Small shifts to higher energies are observed in the oxidized and fixing states. Mo EXAFS of NifV - Kp1 and wild-type in the ''as isolated'' state appear indistinguishable. Curve fitting results best describe the molybdenum in FeMoco as bound by 4-5 S atoms at 2.36 A ,3 Fe atoms at 2.69 A, and 0-2 O(N) atoms at 2.19 A. The spectral similarity of these results concerning the nifV mutant FeMoco structure is discussed

Phase transition of the orthorhombic fluorite-related compounds Ln{sub 3}IrO{sub 7} (Ln = Pr, Nd, Sm, Eu)

Energy Technology Data Exchange (ETDEWEB)

Hinatsu, Yukio, E-mail: hinatsu@sci.hokudai.ac.j [Division of Chemistry, Graduate School of Science, Hokkaido University, Sapporo 060-0810 (Japan); Doi, Yoshihiro; Nishimine, Hiroaki; Wakeshima, Makoto [Division of Chemistry, Graduate School of Science, Hokkaido University, Sapporo 060-0810 (Japan); Sato, Mineo [Department of Chemistry and Chemical Engineering, Faculty of Engineering, Niigata University, 8050 Ikarashi 2-nocho, Niigata 950-2181 (Japan)

2009-12-04

Rare earth iridium oxides Ln{sub 3}IrO{sub 7} (Ln = Pr, Nd, Sm, and Eu) were prepared and their structures were determined by X-ray diffraction measurements. At room temperature, Pr{sub 3}IrO{sub 7} crystallized in an orthorhombic superstructure of cubic fluorite with space group Cmcm. The differential thermal analysis (DTA) and specific heat measurements for Ln{sub 3}IrO{sub 7} (Ln = Pr, Nd, Sm, and Eu) showed a phase transition at 262, 342, 420, and 485 K, respectively. At low temperatures, Ln{sub 3}IrO{sub 7} crystallized in a monoclinic structure with the space group P2{sub 1}/n. The transition temperatures increased with decreasing the ionic radius of rare earths, which indicates that the transition is stress-induced and occurs with the lattice contraction on cooling. These results for Ln{sub 3}IrO{sub 7} were compared with the phase transitions observed for Ln{sub 3}MoO{sub 7}, Ln{sub 3}RuO{sub 7}, Ln{sub 3}ReO{sub 7}, and Ln{sub 3}OsO{sub 7}.

Sr{sub 2}SmNbO{sub 6} perovskite: Synthesis, characterization and density functional theory calculations

Energy Technology Data Exchange (ETDEWEB)

Dutta, Alo, E-mail: alo_dutta@yahoo.com [Department of Condensed Matter Physics and Material Sciences, S. N. Bose National Centre for Basic Sciences, Block-JD, Sector III, Salt Lake, Kolkata, 700106 (India); Mukhopadhyay, P.K. [Department of Condensed Matter Physics and Material Sciences, S. N. Bose National Centre for Basic Sciences, Block-JD, Sector III, Salt Lake, Kolkata, 700106 (India); Sinha, T.P. [Department of Physics, Bose Institute, 93/1 Acharya Prafulla Chandra Road, Kolkata, 700 009 (India); Shannigrahi, Santiranjan [Institute of Materials Research and Engineering, Agency for Science Technology and Research, 3 Research Link, Singapore, 117602 (Singapore); Himanshu, A.K.; Sen, Pintu; Bandyopadhyay, S.K. [Variable Energy Cyclotron Centre, 1/AF Bidhannagar, Kolkata, 700064 (India)

2016-08-15

The density functional theory (DFT) under the generalized gradient approximation (GGA) has been used to investigate the electronic structure of double perovskite oxide Sr{sub 2}SmNbO{sub 6} synthesized by the solid-state reaction technique. The Rietveld refinement of the X-ray diffraction pattern of the sample shows the monoclinic P2{sub 1}/n phase at room temperature. The X-ray photoemission spectrum (XPS) of the material is collected in the energy window of 0–1200 eV. The chemical shift of the constituent elements calculated from the core level XPS spectra is used to analyze the covalency between the O anion and Sm/Nb cations. The valence band (VB) XPS spectrum is compared with the calculated VB spectrum using partial density of states in a standard way. The Raman spectrum is employed to investigate the phonon modes of the material in the monoclinic phase. Lorentzian lines are used to fit the experimental Raman spectrum, which present 24 phonon modes corresponding to the stretching and banding of NbO{sub 6}/SmO{sub 6} octahedra and translational motion of Sr along the Sr−O bond. The discrepancy between the measured and calculated band gap values has been removed by applying modified Becke-Johnson (mBJ) potential in the DFT calculations. The experimental optical band gap obtained from the UV–visible reflectance spectrum is found to be 3.42 eV, which is well matched with the DFT calculated value of 3.2 eV, and suggests the semiconducting nature of the material. The real (ε′) and imaginary (ε″) parts of the optical dielectric constant as a function of energy along the x-, y- and z-polarization directions using mBJ potential are calculated. The collective vibrational modes of the atoms, the Born effective charge of the ions and their effect on the static dielectric constant of the material are studied using DFT. The calculated value of static dielectric constant for SSN is found to be 41.3. - Highlights: • Electronic structure and dynamical

Investigation into catalytic properties of the second group metal molybdates in acrolein oxidation

International Nuclear Information System (INIS)

Yakubovich, M.N.; Gorochovatskij, Ya.B.; Alchazov, T.G.; Adzhamov, K.Yu.

1976-01-01

The catalytic properties are investigated of magnesium, calcium, strontium, zinc, cadmium, and barium molybdates. Temperature dependence of catalysts activity is studied. At temperature over 370 deg C the activity becomes higher in the series ZnMoO 4 -CaMoO 4 -MgMoO 4 -SrMoO 4 . A sharp fall in the activity is observed for BaMoO 4 , and CdMoO 4 . SrMoO 4 is the most active catalyst. The activity series have been made up with respect to the formation of acrylic acid: MgMoO 4 >ZnMoO 4 >CaMoO 4 , and also with respect to the formation of the deep oxidation products: SrMoO 4 >CaMoO 4 >MgMoO 4 >ZnMoO 4 . The dependence of selectivity with respect to the formation of acrylic acid and the sum of the acids on temperature is provided

Methanesulfonates of high-valent metals. Syntheses and structural features of MoO_2(CH_3SO_3)_2, UO_2(CH_3SO_3)_2, ReO_3(CH_3SO_3), VO(CH_3SO_3)_2, and V_2O_3(CH_3SO_3)_4 and their thermal decomposition under N_2 and O_2 atmosphere

International Nuclear Information System (INIS)

Betke, Ulf; Neuschulz, Kai; Wickleder, Mathias S.

2011-01-01

Oxide methanesulfonates of Mo, U, Re, and V have been prepared by reaction of MoO_3, UO_2(CH_3COO)_2.2 H_2O, Re_2O_7(H_2O)_2, and V_2O_5 with CH_3SO_3H or mixtures thereof with its anhydride. These compounds are the first examples of solvent-free oxide methanesulfonates of these elements. MoO_2(CH_3SO_3)_2 (Pbca, a=1487.05(4), b=752.55(2), c=1549.61(5) pm, V=1.73414(9) nm"3, Z=8) contains [MoO_2] moieties connected by [CH_3SO_3] ions to form layers parallel to (100). UO_2(CH_3SO_3)_2 (P2_1/c, a=1320.4(1), b=1014.41(6), c=1533.7(1) pm, β=112.80(1) "c"i"r"c"l"e, V=1.8937(3) nm"3, Z=8) consists of linear UO_2"2"+ ions coordinated by five [CH_3SO_3] ions, forming a layer structure. VO(CH_3SO_3)_2 (P2_1/c, a=1136.5(1), b=869.87(7), c=915.5(1) pm, β=113.66(1) "c"i"r"c"l"e, V=0.8290(2) nm"3, Z=4) contains [VO] units connected by methanesulfonate anions to form corrugated layers parallel to (100). In ReO_3(CH_3SO_3) (P anti 1, a=574.0(1), b=1279.6(3), c=1641.9(3) pm, α=102.08(2), β=96.11(2), γ=99.04(2) "c"i"r"c"l"e, V=1.1523(4) nm"3, Z=8) a chain structure exhibiting infinite O-[ReO_2]-O-[ReO_2]-O chains is formed. Each [ReO_2]-O-[ReO_2] unit is coordinated by two bidentate [CH_3SO_3] ions. V_2O_3(CH_3SO_3)_4 (I2/a, a=1645.2(3), b=583.1(1), c=1670.2(3) pm, β=102.58(3), V=1.5637(5) pm"3, Z=4) adopts a chain structure, too, but contains discrete [VO]-O-[VO] moieties, each coordinated by two bidentate [CH_3SO_3] ligands. Additional methanesulfonate ions connect the [V_2O_3] groups along [001]. Thermal decomposition of the compounds was monitored under N_2 and O_2 atmosphere by thermogravimetric/differential thermal analysis and XRD measurements. Under N_2 the decomposition proceeds with reduction of the metal leading to the oxides MoO_2, U_3O_7, V_4O_7, and VO_2; for MoO_2(CH_3SO_3)_2, a small amount of MoS_2 is formed. If the thermal decomposition is carried out in a atmosphere of O_2 the oxides MoO_3 and V_2O_5 are formed. (Copyright copyright 2011 WILEY-VCH Verlag

Catalytic oxidation of 1,2-DCBz over V2O5/TiO2-CNTs: effect of CNT diameter and surface functional groups.

Science.gov (United States)

Du, Cuicui; Wang, Qiulin; Peng, Yaqi; Lu, Shengyong; Ji, Longjie; Ni, Mingjiang

2017-02-01

A series of V 2 O 5 /TiO 2 -carbon nanotube (CNT) catalysts were prepared and tested to decompose gaseous 1,2-dichlorobenzene (1,2-DCBz). Several physicochemical methods, including nitrogen adsorption, scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and H 2 temperature-programmed reduction (TPR) were employed to characterise their physicochemical properties. To better understand the effect of CNT properties on the reactivity of V 2 O 5 /TiO 2 -CNT catalysts, the 1,2-DCBz residue remaining in the off-gas and on the catalyst surface were both collected and analysed. The results indicate that the outer diameter and the surface functional groups (hydroxide radical and carboxyl) of CNTs significantly influence upon the catalytic activity of CNT-containing V 2 O 5 /TiO 2 catalysts: the CNT outer diameter mainly affects the aggregation of CNTs and the π-π interaction between the benzene ring and CNTs, while the introduction of -OH and -COOH groups by acid treatment can further enlarge specific surface area (SSA) and contribute to a higher average oxidation state of vanadium (V aos ) and supplemental surface chemisorbed oxygen (O ads ). In addition, the enhanced mobility of lattice oxygen (O latt) also improves the oxidation ability of the catalysts.

Highly flexible, conductive and transparent MoO3/Ag/MoO3 multilayer electrode for organic photovoltaic cells

International Nuclear Information System (INIS)

Abachi, T.; Cattin, L.; Louarn, G.; Lare, Y.; Bou, A.; Makha, M.; Torchio, P.

2013-01-01

MoO 3 /Ag/MoO 3 (MAM) multilayer structures were deposited by vacuum evaporation on polyethylene terephthalate (PET) substrate. We demonstrate that, as in the case of glass substrate, the sheet resistance of such structures depends significantly on the Ag film deposition rate. When it is deposited between 0.2 and 0.4 nm/s, an Ag thickness of 11 nm allows achieving sheet resistance of 13 Ω/sq and an averaged transmission of 74%. A study of the influence of the PET substrate on the optimum MoO 3 thicknesses was done. A good qualitative agreement between the theoretical calculations of the variation of the optical transmittance of the MoO 3 /Ag/MoO 3 structures is obtained. The optimum MAM structures MoO 3 (17.5 nm)/Ag (11 nm)/MoO 3 (35 nm) has a factor of merit F M = 4.21 10 −3 (Ω/sq) −1 . Proven by the scotch test the MAM structures exhibit a good adhesion to the PET substrates. The MAM structures were also submitted to bending tests. For outer bending, the samples exhibit no variation of their resistance value, while for inner bending there is a small increase of the resistance of the MAM structures. However this increasing is smaller than that exhibited by Indium Tin Oxide. When the PET/MAM structures are used as anode in organic photovoltaic cells, it is shown that the need to use thicker Ag films inside the multilayer and to cover the MAM with Au to obtain promising Current density vs Voltage characteristics is due to the heating of the PET substrate during the deposition process. - Highlights: • MoO 3 /Ag/MoO 3 structures deposited on polyethylene terephthalate substrate. • MoO 3 /Ag/MoO 3 structures deposited by vacuum evaporation. • The Ag deposition rate influences the properties of the structures. • The MoO 3 /Ag/MoO 3 optimum structure has a factor of merit F M = 4.21 10 −3 (Ω/sq) −1 . • The MoO 3 /Ag/MoO 3 structures exhibit a high flexibility

Characterization of Donut-Like SrMoO4 Produced by Microwave-Hydrothermal Process

Directory of Open Access Journals (Sweden)

Surangkana Wannapop

2013-01-01

Full Text Available SrMoO4 hierarchical nanostructures were successfully produced by a one step of 270 W microwave-hydrothermal process of one of the solutions containing three strontium salts [Sr(NO32, Sr(CH3CO22, and SrCl2·6H2O] and (NH46Mo7O24·4H2O for different lengths of time. The as-produced products were characterized by X-ray diffraction, electron microscopy, and spectroscopy. In this research, they were primitive tetragonal structured donut-like SrMoO4, with the main 881 cm−1  ν1(Ag symmetric stretching vibration mode of [MoO4]2− units and 3.92 eV energy gap.

In situ catalytic growth of large-area multilayered graphene/MoS2 heterostructures

Science.gov (United States)

Fu, Wei; Du, Fei-Hu; Su, Juan; Li, Xin-Hao; Wei, Xiao; Ye, Tian-Nan; Wang, Kai-Xue; Chen, Jie-Sheng

2014-04-01

Stacking various two-dimensional atomic crystals on top of each other is a feasible approach to create unique multilayered heterostructures with desired properties. Herein for the first time, we present a controlled preparation of large-area graphene/MoS2 heterostructures via a simple heating procedure on Mo-oleate complex coated sodium sulfate under N2 atmosphere. Through a direct in situ catalytic reaction, graphene layer has been uniformly grown on the MoS2 film formed by the reaction of Mo species with S pecies, which is from the carbothermal reduction of sodium sulfate. Due to the excellent graphene ``painting'' on MoS2 atomic layers, the significantly shortened lithium ion diffusion distance and the markedly enhanced electronic conductivity, these multilayered graphene/MoS2 heterostructures exhibit high specific capacity, unprecedented rate performance and outstanding cycling stability, especially at a high current density, when used as an anode material for lithium batteries. This work provides a simple but efficient route for the controlled fabrication of large-area multilayered graphene/metal sulfide heterostructures with promising applications in battery manufacture, electronics or catalysis.

Spherical α-MnO2 Supported on N-KB as Efficient Electrocatalyst for Oxygen Reduction in Al–Air Battery

Directory of Open Access Journals (Sweden)

Kui Chen

2018-04-01

Full Text Available Traditional noble metal platinum (Pt is regarded as a bifunctional oxygen catalyst due to its highly catalytic efficiency, but its commercial availability and application is often restricted by high cost. Herein, a cheap and effective catalyst mixed with α-MnO2 and nitrogen-doped Ketjenblack (N-KB (denoted as MnO2-SM150-0.5 is examined as a potential electrocatalyst in oxygen reduction reactions (ORR and oxygen evolution reactions (OER. This α-MnO2 is prepared by redox reaction between K2S2O8 and MnSO4 in acid conditions with a facile hydrothermal process (named the SM method. As a result, MnO2-SM150-0.5 exhibits a good catalytic performance for ORR in alkaline solution, and this result is comparable to a Pt/C catalyst. Moreover, this catalyst also shows superior durability and methanol tolerance compared with a Pt/C catalyst. It also displays a discharge voltage (~1.28 V at a discharge density of 50 mA cm−2 in homemade Al–air batteries that is higher than commercial 20% Pt/C (~1.19 V. The superior electrocatalytic performance of MnO2-SM150-0.5 could be attributed to its higher Mn3+/Mn4+ ratio and the synergistic effect between MnO2 and the nitrogen-doped KB. This study provides a novel strategy for the preparation of an MnO2-based composite electrocatalyst.

PREPARATION, CHARACTERIZATION, ACTIVITY, DEACTIVATION, AND REGENERATION TESTS OF CoO-MoO/ZnO AND CoO-MoO/ZnO-ACTIVATED ZEOLITE CATALYSTS FOR THE HYDROGEN PRODUCTION FROM FUSEL OIL

Directory of Open Access Journals (Sweden)

Wega Trisunaryanti

2010-06-01

Full Text Available Preparation, characterization, activation, deactivation, and regeneration tests of CoO-MoO/ZnO and CoO-MoO/ZnO-Activated Zeolite (AZ catalysts for the hydrogen production using steam reforming of alcohols in fusel oil have been conducted. Both catalysts were prepared by impregnation of Co and Mo onto ZnO or ZnO-AZ powder then followed by calcination at 400 °C for 5 h under N2 stream. The BET method and pyridine adsorption were used for catalysts characterization. The study of activation, deactivation, and regeneration of catalysts were conducted by using steam reforming method in the semi flow reactor. The reaction condition were: weight ratio of catalysts/feed = 0.1, temperature: 450 °C, duration: 45 min. The gas product was trapped in a 250 mL vacuum pyrex bottle filled with 50 mL of 4 M NaOH solution and analyzed by GC with TCD system to determine H2 existance and HCl titration to determine CO2 produced during the process that was dissolved in NaOH solution. The results showed that CoO-MoO/ZnO-AZ catalyst produced higher gas conversion than CoO-MoO/ZnO catalyst. However, it had short catalyst lifetime due to its high amount of coke deposited during the process. The regeneration test could enhance the catalyst activity. The gas product consisted of H2 (14.70% and CO2 (24.41%.   Keywords: fusel oil, steam reforming, deactivation, regeneration, hydrogen production.

Measurement of the molar heat capacities of MoO2 and MoO3 from 350 to 950 K

International Nuclear Information System (INIS)

Inaba, H.; Miyahara, K.; Naito, K.

1984-01-01

Molar heat capacities of MoO 2 and MoO 3 were measured in the range between 350 and 950 K by means of adiabatic scanning calorimetry. For MoO 2 , a sharp heat-capacity anomaly with a molar enthalpy change of (178 +- 24) J.mol -1 and a molar entropy change of (0.207 +- 0.028) J.K -1 .mol -1 was observed at 865 K, which had not been detected by drop calorimetry. For MoO 3 , two heat-capacity anomalies with molar enthalpy changes of (88 +- 21) and (60 +- 36) J.mol -1 were found at 808 K and 857 K, respectively; neither anomaly had been detected by the drop method. The lattice molar heat capacities of MoO 2 and MoO 3 are estimated as Csub(l,m)(MoO 2 ) = D(469 K/T) + E(578 K/T) + E(876 K/T) and Csub(l,m)(MoO 3 ) = D(208 K/T) + 2E(488 K/T) + E(1170 K/T), where D(x) and E(x) are the Debye and Einstein functions, respectively. The temperature coefficient of the electronic molar heat capacity of MoO 2 is estimated as (6.0 +- 0.5) mJ.K -2 .mol -1 . The excess heat capacity in MoO 3 found at higher temperatures is interpreted as being due to vacancy formation with a molar activation energy of (98 +-5) kJ.mol -1 . The origin of the heat-capacity anomalies is inferred as arising from the slight movement of distorted MoO 6 octahedra in the MoO 2 and MoO 3 structures. (author)

Using of catalytic effect of Mo(VI) on mutual metamorphosis o 2-ketoses and 2-C-(hydroxymethyl)aldoses

International Nuclear Information System (INIS)

Hricoviniova, Z.; Petrus, L.

1999-01-01

Influence of catalytic effect of the Mo(VI) was studied after mutual metamorphosis of two groups of saccharides: 2-ketoses and 2-C-(hydroxymethyl)aldoses. Metamorphosis is connected with change of configuration at the atom neighbouring with the carbonyl group of the saccharide. The mechanism of stereospecific transformation of 2-ketoses on 2-C-(hydroxymethyl)aldose was studied with 13 C-isotopic substituted 2-ketoses.It was confirmed that it is intramolecular process. This reaction was studied on pentuloses, hexuloses, heptuloses as well as on responsive 2-C-(hydroxymethyl)aldoses

Influence of H2O and H2S on the Composition, Activity, and Stability of Sulfided Mo, CoMo, and NiMo Supported on MgAl2O4 for Hydrodeoxygenation of Ethylene Glycol

DEFF Research Database (Denmark)

Dabros, Trine Marie Hartmann; Gaur, Abhijeet; Pintos, Delfina Garcia

2018-01-01

In this work, density functional theory (DFT), catalytic activity tests, and in-situ X-ray absorption spectroscopy (XAS) was performed to gain detailed insights into the activity and stability of MoS2, Ni-MoS2, and Co-MoS2 catalysts used for hydrodeoxygenation (HDO) of ethylene glycol upon...

Spatial decoupling of light absorption and catalytic activity of Ni-Mo-loaded high-aspect-ratio silicon microwire photocathodes

Science.gov (United States)

Vijselaar, Wouter; Westerik, Pieter; Veerbeek, Janneke; Tiggelaar, Roald M.; Berenschot, Erwin; Tas, Niels R.; Gardeniers, Han; Huskens, Jurriaan

2018-03-01

A solar-driven photoelectrochemical cell provides a promising approach to enable the large-scale conversion and storage of solar energy, but requires the use of Earth-abundant materials. Earth-abundant catalysts for the hydrogen evolution reaction, for example nickel-molybdenum (Ni-Mo), are generally opaque and require high mass loading to obtain high catalytic activity, which in turn leads to parasitic light absorption for the underlying photoabsorber (for example silicon), thus limiting production of hydrogen. Here, we show the fabrication of a highly efficient photocathode by spatially and functionally decoupling light absorption and catalytic activity. Varying the fraction of catalyst coverage over the microwires, and the pitch between the microwires, makes it possible to deconvolute the contributions of catalytic activity and light absorption to the overall device performance. This approach provided a silicon microwire photocathode that exhibited a near-ideal short-circuit photocurrent density of 35.5 mA cm-2, a photovoltage of 495 mV and a fill factor of 62% under AM 1.5G illumination, resulting in an ideal regenerative cell efficiency of 10.8%.

{alpha}-Sb{sub 2}O{sub 4}-induced improvements of the catalytic behavior of MoO{sub 3}-(010) in the oxygen-assisted dehydration of 2-butanol: implications in selective oxidation

Energy Technology Data Exchange (ETDEWEB)

Gaigneaux, E.M. [Fonds National de la Recherche Scientifique of Belgium (Belgium); Naeye, M.L.; Dupont, O.; Ruiz, P.; Delmon, B. [Unite de Catalyse et Chimie des Materiaux Divises, Universite Catholique de Louvain, Louvain-La-Neuve (Belgium); Callant, M.; Kartheuser, B. [CERTECH, Senefffe (Belgium)

1998-12-31

This article concerns the synergetic effects between an MoO{sub 3} sample composed of crystallites exposing preferentially the (010) basal faces and {alpha}-Sb{sub 2}O{sub 4} in the oxygen-assisted dehydration of 2-butanol at 220 C. The conversion of 2-butanol and the yield to butene improved when MoO{sub 3} was reacted in the presence of {alpha}-Sb{sub 2}O{sub 4}. The origin of the synergism is discussed. When reacted in the absence of {alpha}-Sb{sub 2}O{sub 4}, MoO{sub 3} got over-reduced and fragmented to MoO{sub 2}. MoO{sub 2} is intrinsically less active than MoO{sub 3} thus explaining that the deep reduction of MoO{sub 3} corresponds to its tendency to deactivate. In the presence of {alpha}-Sb{sub 2}O{sub 4}, the formation of MoO{sub 2} is inhibited with, as a consequence, the absence of deactivation. This leads to the synergetic effects obtained with the mechanical mixture of MoO{sub 3} with {alpha}-Sb{sub 2}O{sub 4}. (orig.)

High Efficient Photo-Fenton Catalyst of α-Fe2O3/MoS2 Hierarchical Nanoheterostructures: Reutilization for Supercapacitors

Science.gov (United States)

Yang, Xijia; Sun, Haiming; Zhang, Lishu; Zhao, Lijun; Lian, Jianshe; Jiang, Qing

2016-08-01

A novel three-dimensional (3D) α-Fe2O3/MoS2 hierarchical nanoheterostructure is effectively synthesized via a facile hydrothermal method. The zero-dimensional (0D) Fe2O3 nanoparticles guide the growth of two-dimensional (2D) MoS2 nanosheets and formed 3D flower-like structures, while MoS2 facilitates the good dispersion of porous Fe2O3 with abundant oxygen vacancies. This charming 3D-structure with perfect match of non-equal dimension exhibits high recyclable photo-Fenton catalytic activity for Methyl orange pollutant and nice specific capacity in reusing as supercapacitor after catalysis. The synergistic effect between Fe2O3 and MoS2, the intermediate nanointerfaces, the 3D porous structures, and the abundant oxygen vacancies both contribute to highly active catalysis, nice electrochemical performance and stable cycling. This strategy is simple, cheap, and feasible for maximizing the value of the materials, as well as eliminating the secondary pollution.

Impact of Reduced Graphene Oxide on MoS2 Grown by Sulfurization of Sputtered MoO3 and Mo Precursor Films (Postprint)

Science.gov (United States)

2016-05-26

1,2 intercalation assisted exfoliation,8–11 physical vapor deposition (PVD),12,13 and a wet chemistry approach involving thermal decomposition of a... annealed MoO3, MoS2 films S1 (MoS2 using Mo precursor), S2 (MoS2 using MoO3 precursor), S1r (MoS2 using Mo pre- cursor and rGO), and S2r (MoS2 using...MoO3 precursor and rGO). The annealed MoO3 (a) shows Mo(IV) peaks which are indicative of MoO2, and Mo(VI) peaks that occur when MoO3 is present. Both

Study of the R-(Zr,W)-(O,N) (R = Y, Nd, Sm, Gd, Yb) oxynitride system

Energy Technology Data Exchange (ETDEWEB)

Tessier, Franck, E-mail: Franck.Tessier@univ-rennes1.fr [UMR CNRS 6226 ' Sciences Chimiques de Rennes' , equipe ' Verres et Ceramiques' , Universite de Rennes 1, 35042 Rennes cedex (France); Maillard, Pascal [UMR CNRS 6226 ' Sciences Chimiques de Rennes' , equipe ' Verres et Ceramiques' , Universite de Rennes 1, 35042 Rennes cedex (France); Orhan, Emmanuelle [Laboratoire Science des Procedes Ceramiques et Traitements de Surface, UMR CNRS 6638, Universite de Limoges, 123 Avenue Albert Thomas, 87060 Limoges cedex (France); Chevire, Francois [UMR CNRS 6226 ' Sciences Chimiques de Rennes' , equipe ' Verres et Ceramiques' , Universite de Rennes 1, 35042 Rennes cedex (France)

2010-02-15

The replacement of tantalum by the couple Zr/W within the RTa-O-N systems (R = Y, Nd, Sm, Gd, Yb), enables the preparation of novel oxide and oxynitride phases in the R-Zr-W-O-N system. R{sub 2}Zr{sub 2-x}W{sub x}O{sub 7+x} oxides exhibit the fluorite-type (x < 0.9) and scheelite (x {approx} 1) structures. Corresponding oxynitride compositions are of the fluorite-type and show different colors, for example in the case of ytterbium: pale yellow (x = 0.2 or 0.25), green (x = 0.5-0.8) and brown for the tungsten-rich samples (x = 0.9, 1). Photocatalytic activity measurements have been performed to investigate the overall water splitting behavior of these colored phases.

Synthesis, structure and electrochemical properties of polyaniline/MoO3 nanobelt composite for lithium battery

International Nuclear Information System (INIS)

Mohan, Varishetty Madhu; Chen, Wen; Murakami, Kenji

2013-01-01

Graphical abstract: Hydrothermal method was introduced for the synthesis of MoO 3 nanobelts and polyaniline (PANI)/MoO 3 nanobelt composites. The structure and morphology of the samples were studied by X-ray diffraction (XRD), Fourier transform infrared radiation (FTIR), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analysis. We can see the presence of polyaniline on the MoO 3 nanobelts surface in the TEM pictures as shown in Fig. (a). The pure MoO 3 nanobelts exhibit the initial specific capacity 276 mAhg −1 , whereas PANI/MoO 3 nanobelt composite shows little low initially 228 mAhg −1 after that it has more stabilized specific capacity with increasing cycle numbers as shown in Fig. (b). The cyclic voltammograms of the PANI/MoO 3 nanobelt composite show better cyclic performance compared to pure MoO 3 nanobelts. The electrochemical impedance spectres were studied for both the pure and PANI/MoO 3 samples at 2.0 and 3.5 potentials. The role of the PANI polymeric component of the composite material seems to be the stabilization of the specific capacity due to probable homogeneous distribution of the induced stress during cycling. Display Omitted Highlights: ► Hydrothermal synthesis of MoO 3 , PANI/MoO 3 nanobelts. ► Samples were characterised by XRD, FTIR, DSC, SEM, TEM, CV and impedance. ► MoO 3 nanobelts cathode battery shows initial specific capacity 276 mAhg −1 . ► PANI/MoO 3 nanobelts show initial specific capacity 228 mAhg −1 but high stability. ► PANI/MoO 3 sample studies by impedance at the potentials of 2.0 and 3.5 V. -- Abstract: The MoO 3 nanobelts and polyaniline (PANI)/MoO 3 nanobelt composite were synthesized using hydrothermal method. The crystal structure and morphology of the samples were studied by X-ray diffraction (XRD), Fourier transform infrared radiation (FTIR), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Differential scanning calorimetric (DSC) and thermo

High index surfaces of Au-nanocrystals supported on one-dimensional MoO3-nanorod as a bi-functional electrocatalyst for ethanol oxidation and oxygen reduction

International Nuclear Information System (INIS)

Karuppasamy, L.; Chen, C.Y.; Anandan, S.; Wu, J.J.

2017-01-01

Highlights: •Synthesis of a new class of Au nanocrystals enclosed with high index surface supported on MoO 3 nanorods by ultrasonic probe method. •The role of supporting materials reduces the loading of Au and acts as a co-catalyst. •The as prepared electrocatalyst exhibits enhanced catalytic activity and stability towards both EOR and ORR. -- Abstract: The design of highly active electrocatalyst for ethanol electrooxidation (EOR) and oxygen reduction reaction (ORR) is of great significance for the improvement of efficient direct ethanol fuel cells (DEFCs). Therefore, creating high index facets nanocrystals with abundant catalytic active sites of stepped atoms is an effective way to enhance the electrocatalytic performance. In this article, we prepared the high index surface structures of Au nanocrystals supported on one-dimensional (1-D) MoO 3 nanorods by using two steps ultrasonic probe irradiation method. The size and physical properties of as electrocatalysts were studied by using field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM), and x-ray diffraction (XRD) instrumentation. Besides, the catalytic activity of as Au-MoO 3 electrocatalyst was determined by using cyclic voltammetry (CV), chronoamperometric (CA), electrochemical impedance spectroscopy (EIS), CO-stripping, and linear sweep voltammetry-rotating disk electrode (LSV-RDE). As a consequence, the Au-MoO 3 nanocomposites has been considered as an effective electrocatalyst for both ethanol oxidation and oxygen reduction reaction.

High Temperature NMR Studies of the Glass-Crystal Transition in the Cs2S2O7-V2O5 System

DEFF Research Database (Denmark)

Lapina, Olga B.; Terskikh, Viktor V.; Shubin, Aleksander A.

1997-01-01

133Cs and 51V NMR spectra have been recorded of Cs2S2O7 and the catalytically important Cs2S2O7-V2O5 mixtures in the temperature range 20 - 550 C. A high mobility of Cs+ in the solid Cs2S2O7 was observed. The transformation from glassy state to crystalline state was investigated for the compositi...

Optical properties of CaWO4 and CaMoO4 crystals in the 4-25 eV region

International Nuclear Information System (INIS)

Grasser, R.; Pitt, E.; Scharmann, A.; Zimmerer, G.

1975-04-01

The reflection spectra of CaWO 4 and CaMoO 4 single crystals were measured in the region between 4 and 25 eV. The measurements were performed using the electron synchrotron DESY as a light source. Both crystals show very similar spectral features. A relatively sharp, well separated low energy peak is accompanied on the high energy side by two groups of maxima, each group containing three broad main reflection bands which strongly overlap. Besides this, a less pronounced structure is observed over the whole spectral region. The experimental results are discussed in terms of semiempirical MO calculations of the anionic transition metal oxo complexes. (orig.) [de

Microwave-assisted synthesis of graphene/CoMoO4 nanocomposites with enhanced supercapacitor performance

International Nuclear Information System (INIS)

Xu, Xiaowei; Shen, Jianfeng; Li, Na; Ye, Mingxin

2014-01-01

Highlights: • RGO/CoMoO 4 nanocomposites are prepared by microwave irradiation for the first time. • RGO/CoMoO 4 nanocomposites show a high specific capacitance of 322.5 F g −1 . • Enhanced electrical conductivity leads to superior electrochemical performance. • Low crystallinity of CoMoO 4 is favorable to improve the electrochemical performance. - Abstract: A facile and efficient strategy for preparing reduced graphene oxide–cobalt molybdate (RGO/CoMoO 4 ) nanocomposites assisted by microwave irradiation for the first time is demonstrated. The resulting nanocomposites are comprised of CoMoO 4 nanoparticles that are well-anchored on graphene sheets by in situ reducing. The prepared RGO/CoMoO 4 nanocomposites have been thoroughly characterized by Fourier-transform infrared spectroscopy, X-ray diffraction, Raman spectroscopy, thermogravimetric analysis, scanning electron microscopy and X-ray photoelectron spectroscopy. Importantly, the prepared nanocomposites exhibit excellent electrochemical performance for supercapacitors. Results show that RGO/CoMoO 4 nanocomposites exhibited much better electrochemical capability than pure-CoMoO 4 and RGO/CoMoO 4 for annealing. RGO/CoMoO 4 nanocomposites with 37.4 wt% CoMoO 4 content achieved a specific capacitance about 322.5 F g −1 calculated from the CV plots at 5 mV s −1 , which was higher than that of pure-CoMoO 4 (95.0 F g −1 ) and RGO/CoMoO 4 for annealing (102.5 F g −1 ). The good electrochemical performance can be attributed to the synergistic effects of the individual components

Studying effect of MoO{sub 3} on elastic and crystallization behavior of lithium diborate glasses

Energy Technology Data Exchange (ETDEWEB)

Shaaban, KH.S.; Abd Elnaeim, A.M. [El-Azhar University, Physics Department, Faculty of Science, Assiut (Egypt); Abo-naf, S.M. [National Research Centre, Glass Research Department, Cairo (Egypt); Hassouna, M.E.M. [Beni-Suef University, Chemistry Department, Faculty of Science, Beni Suef (Egypt)

2017-06-15

The effect of MoO{sub 3} addition on the crystallization characteristics of 2Al{sub 2}O{sub 3}-23Li{sub 2}O-(75 - x) B{sub 2}O{sub 3} glass (where x MoO{sub 3} = 0, 10, 20, and 40 mol %) has been investigated. The compositional dependence of the glass transition (T{sub g}), and crystallization (T{sub c}) temperatures was determined by the differential thermal analysis (DTA). It was found that both the T{sub g} and T{sub c} decrease with increasing MoO{sub 3} content. The amorphous nature of the as-quenched glass and crystallinity of the produced glass-ceramics were confirmed by X-ray powder diffraction (XRD) analysis. Glass-ceramics embedded with diomignite (lithium diborate, Li{sub 2}B{sub 4}O{sub 7}) were produced from all investigated glasses by heat-treating the as-quenched glasses at the appropriate temperatures obtained from the DTA traces. Addition of MoO{sub 3} to the glass composition at 10% MoO{sub 3}, causes the formation of lithium molybdenum oxide (Li{sub 4}MoO{sub 5}) crystalline phase in addition to the diomignite phase. Increasing MoO{sub 3} content to 20% causes a phase transformation of lithium molybdenum oxide from the (Li{sub 4}MoO{sub 5}) to the (Li{sub 2}MoO{sub 4}) phase and the formation of another lithium borate (Li{sub 4}B{sub 2}O{sub 5}) phase in addition to the diomignite. Further increase of MoO{sub 3} content to 40% results in another phase transformation to the lithium aluminum molybdenum oxide [LiAl(MoO{sub 4}){sub 2}], and, in this case, the molybdenum content was excess enough to crystallize the molybdate (MoO{sub 3}) itself. Scanning electron microscopy (SEM) was used to characterize the morphology and microstructure of the formed solid solution phases. The values of the T{sub g} decrease with increasing the MoO{sub 3} content. The ultrasonic wave velocities and elastic moduli were determined using the pulse-echo method. Both velocities (v{sub L} and v{sub T}) were increased as the MoO{sub 3} content, this increase can be

Study to improve the quality of a Mexican straight run gasoil over NiMo/γ-Al2O3 catalysts

International Nuclear Information System (INIS)

Dominguez-Crespo, M.A.; Diaz-Garcia, L.; Arce-Estrada, E.M.; Torres-Huerta, A.M.; Cortez de la Paz, M.T.

2006-01-01

Four NiMo catalyst supported on Al 2 O 3 with different textural properties have been studied in the hydrodesulfurization (HDS), hydrodenitrogenation (HDN) and hydrodearomatization (HDA) of a Mexican straight run gasoil (SRGO). All reactions were carried out at three different temperatures 613, 633, and 653 K. Alumina supports were analysed by pyridine FTIR-TPD and nitrogen physisorption in order to determine their surface acidity and textural properties, respectively. TPR studies of the NiMo catalysts were analysed to correlate their hydrogenating properties. Metallic particles were characterized (after sulfidation) using transmission electron microscopy (TEM). Catalytic activities are discussed in relation to the physicochemical properties of NiMo catalysts. The importance of textural properties on coke deposition has been emphasized. The results of catalytic activity of these materials varied depending on dispersed MoS particles and pore distribution in final catalysts. The optimum pore diameter was found around 80 A for HDS and HDN

Study to improve the quality of a Mexican straight run gasoil over NiMo/γ-Al 2O 3 catalysts

Science.gov (United States)

Domínguez-Crespo, M. A.; Díaz-García, L.; Arce-Estrada, E. M.; Torres-Huerta, A. M.; Cortéz-De la Paz, M. T.

2006-11-01

Four NiMo catalyst supported on Al 2O 3 with different textural properties have been studied in the hydrodesulfurization (HDS), hydrodenitrogenation (HDN) and hydrodearomatization (HDA) of a Mexican straight run gasoil (SRGO). All reactions were carried out at three different temperatures 613, 633, and 653 K. Alumina supports were analysed by pyridine FTIR-TPD and nitrogen physisorption in order to determine their surface acidity and textural properties, respectively. TPR studies of the NiMo catalysts were analysed to correlate their hydrogenating properties. Metallic particles were characterized (after sulfidation) using transmission electron microscopy (TEM). Catalytic activities are discussed in relation to the physicochemical properties of NiMo catalysts. The importance of textural properties on coke deposition has been emphasized. The results of catalytic activity of these materials varied depending on dispersed MoS particles and pore distribution in final catalysts. The optimum pore diameter was found around 80 Å for HDS and HDN.

Neutronic feasibility studies using U-Mo dispersion fuel (9 Wt % Mo, 5.0 gU/cm3) for LEU conversion of the MARIA (Poland), IR-8 (Russia), and WWR-SM (Uzbekistan) research reactors

International Nuclear Information System (INIS)

Bretscher, M.M.; Deen, J.R.; Hanan, N.A.; Matos, E.

2000-01-01

U-Mo alloys dispersed in an Al matrix offer the potential for high-density uranium fuels needed for the LEU conversion of many research reactors. On-going fuel qualification tests by the US RERTR Program show good irradiation properties of U-Mo alloy dispersion fuel containing 7-10 weight percent molybdenum. For the neutronic studies in this paper the alloy was assumed to contain 9 wt % Mo (U-9Mo) with a uranium density in the fuel meat of 5.00 gU/cm 3 which corresponds to 32.5 volume % U-9Mo. Fuels containing U-9Mo have been used in Russian reactors since the 1950's. For the three research reactors analyzed here, LEU fuel element thicknesses are the same as those for the Russian-fabricated HEU reference fuel elements. Relative to the reference fuels containing 80-90% enriched uranium, LEU U-9Mo Al-dispersion fuel with 5.00 gU/cm 3 doubles the cycle length of the MARIA reactor and increases the IR-8 cycle length by about 11%. For the WWR-SM reactor, the cycle length, and thus the number of fuel assemblies used per year, is nearly unchanged. To match the cycle length of the 36% enriched fuel currently used in the WWR-SM reactor will require a uranium density in the LEU U-9Mo Al-dispersion fuel of about 5.4 gU/cm 3 . The 5.00 gU/cm 3 LEU fuel causes thermal neutron fluxes in water holes near the edge of the core to decrease by (6-8)% for all three reactors. (author)

X-ray and electron microscopy investigation of the topotactic transformation of MoO3 into MoO2

International Nuclear Information System (INIS)

Bertrand, O.; Dufour, L.C.

1980-01-01

The reduction of MoO 3 is investigated by X-ray analysis and electron microscopy from MoO 3 (010) platelets between 1000 A and 5 mm long. In all cases, the following orientation relationship between both lattices is found: [100] 2 parallel [010] 3 , [122] 2 parallel [100] 3 . [-12-2] 2 parallel [001] 3 . MoO 3 crystallites twinning and misorientation are discussed in relation with the particular importance of [101] 3 directions in MoO 3 preserved in the transformation and becoming [010] 2 of MoO 2 . A model for this topotactic reduction is proposed where the reaction develops layer (010) 3 by layer (010) 3 to form [20-1] 2 type planes in MoO 2 structure. Data on the kinetics of the boundary moving in [010] 3 direction are also presented. (author)

Chemistry and engineering of catalytic hydrodesulfurization

NARCIS (Netherlands)

Schuit, G.C.A.; Gates, B.C.

1973-01-01

A review with 74 refs. on catalytic hydrodesulfurization of pure compds. and petroleum feedstocks, with emphasis on reaction intermediates and structures of Al2O3-supported Ni-W and Co-Mo catalysts. [on SciFinder (R)

Preparation of MoS2/TiO2 based nanocomposites for photocatalysis and rechargeable batteries: progress, challenges, and perspective.

Science.gov (United States)

Chen, Biao; Meng, Yuhuan; Sha, Junwei; Zhong, Cheng; Hu, Wenbin; Zhao, Naiqin

2017-12-21

The rapidly increasing severity of the energy crisis and environmental degradation are stimulating the rapid development of photocatalysts and rechargeable lithium/sodium ion batteries. In particular, MoS 2 /TiO 2 based nanocomposites show great potential and have been widely studied in the areas of both photocatalysis and rechargeable lithium/sodium ion batteries due to their superior combination properties. In addition to the low-cost, abundance, and high chemical stability of both MoS 2 and TiO 2 , MoS 2 /TiO 2 composites also show complementary advantages. These include the strong optical absorption of TiO 2 vs. the high catalytic activity of MoS 2 , which is promising for photocatalysis; and excellent safety and superior structural stability of TiO 2 vs. the high theoretic specific capacity and unique layered structure of MoS 2 , thus, these composites are exciting as anode materials. In this review, we first summarize the recent progress in MoS 2 /TiO 2 -based nanomaterials for applications in photocatalysis and rechargeable batteries. We highlight the synthesis, structure and mechanism of MoS 2 /TiO 2 -based nanomaterials. Then, advancements and strategies for improving the performance of these composites in photocatalytic degradation, hydrogen evolution, CO 2 reduction, LIBs and SIBs are critically discussed. Finally, perspectives on existing challenges and probable opportunities for future exploration of MoS 2 /TiO 2 -based composites towards photocatalysis and rechargeable batteries are presented. We believe the present review would provide enriched information for a deeper understanding of MoS 2 /TiO 2 composites and open avenues for the rational design of MoS 2 /TiO 2 based composites for energy and environment-related applications.

Catalytic hydroliquefaction of biomass with red mud and CoO-MoO sub 3 catalysts

Energy Technology Data Exchange (ETDEWEB)

Klopries, B.; Hodek, W.; Bandermann, F. (Universitaet-Gesamthochschule Essen, Essen (Germany, F.R.). Inst. fuer Technische Chemie)

1990-04-01

Rye straw was completely hydroliquefied, using red mud or CoO-MoO{sub 3} as the catalyst. Red mud catalyst exhibited a satisfactory activity only in the presence of sulphur at {approx} 673 K. Depending on reaction conditions, different amounts of gaseous and liquid products were formed. Their product distributions were comparable to those obtained in hydroliquefaction of cellulose and lignin. All results could be described by a model which assumed that: pyrolysis precedes hydrogenation of pyrolysis products; CO and CO{sub 2} are products of pyrolysis reaction; and hydrogen is consumed mainly in hydrodeoxygenation reactions. Therefore, from a practical point of view, red mud, which is known as a coal liquefaction catalyst, can also be recommended as a cheap and powerful catalyst in the hydroliquefaction of biomass. 29 refs., 6 figs., 11 tabs.

Band alignment of ZnO/multilayer MoS{sub 2} interface determined by x-ray photoelectron spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Liu, Xinke, E-mail: xkliu@szu.edu.cn, E-mail: liuwj@szu.edu.cn; He, Jiazhu; Chen, Le; Li, Kuilong; Jia, Fang; Zeng, Yuxiang; Lu, Youming; Zhu, Deliang; Liu, Wenjun, E-mail: xkliu@szu.edu.cn, E-mail: liuwj@szu.edu.cn [College of Materials Science and Engineering, Nanshan District Key Lab for Biopolymer and Safety Evaluation, Shenzhen University, 3688 Nanhai Ave, Shenzhen 518060 (China); Zhang, Yuan [School of Physics and Electronic Information, Hua Bei Normal University, 100 Dongshan Road, Huai Bei 235000 (China); Liu, Qiang; Yu, Wenjie [State Key Laboratory of Functional Materials for Informatics, Shanghai Institute of Microsystem and Information Technology, CAS, 865 Chang Ning Road, Shanghai 200050 (China); Wu, Jing [Institute of Materials research and Engineering (IMRE), 2 Fusionopolis Way, Innovis, #08-03, 138634 Singapore (Singapore); He, Zhubing [Department of Materials Science and Engineering, South University of Science and Technology of China, 1088 Xueyuan Road, Shenzhen 518055 (China); Ang, Kah-Wee [Department of Electrical and Computer Engineering, National University of Singapore, 4 Engineering Drive 3, 117583 Singapore (Singapore)

2016-08-15

The energy band alignment between ZnO and multilayer (ML)-MoS{sub 2} was characterized using high-resolution x-ray photoelectron spectroscopy. The ZnO film was deposited using an atomic layer deposition tool, and ML-MoS{sub 2} was grown by chemical vapor deposition. A valence band offset (VBO) of 3.32 eV and a conduction band offset (CBO) of 1.12 eV were obtained for the ZnO/ML-MoS{sub 2} interface without any treatment. With CHF{sub 3} plasma treatment, a VBO and a CBO across the ZnO/ML-MoS{sub 2} interface were found to be 3.54 eV and 1.34 eV, respectively. With the CHF{sub 3} plasma treatment, the band alignment of the ZnO/ML-MoS{sub 2} interface has been changed from type II or staggered band alignment to type III or misaligned one, which favors the electron-hole pair separation. The band alignment difference is believed to be dominated by the down-shift in the core level of Zn 2p or the interface dipoles, which is caused by the interfacial layer rich in F.

Influence of Nitrogen Partial Pressure on Microstructure and Tribological Properties of Mo-Cu-V-N Composite Coatings with High Cu Content

Directory of Open Access Journals (Sweden)

Haijuan Mei

2018-01-01

Full Text Available In this study, Mo-Cu-V-N composite coatings with high Cu content of ~18 at.% were deposited on 316L stainless steel and YT14 cemented carbide substrates by high power impulse magnetron sputtering in Ar–N2 gas mixtures. The influence of N2 partial pressure was investigated with respect to the microstructure and tribological properties of the coatings. The results indicated that the Mo-Cu-V-N composite coatings exhibited FCC B1-MoN phase with a strong (200 preferred orientation, and Cu phase was found to exist as metallic species. As the N2 partial pressure increased from 0.11 to 0.35 Pa, the peak intensity of (200 plane decreased gradually and simultaneous peak broadening was observed, which was typical for grain refinement. With increasing the N2 partial pressure, the columnar microstructure became much coarser, which led to the decrease of residual stress and hardness. The Mo-Cu-V-N composite coatings with high Cu content exhibited a relatively low wear rate of 10−8 mm3/N·m at 25 °C, which was believed to be attributed to the mixed lubricious oxides of MoO2, CuO and V2O5 formed during tribo-oxidation, which cannot be formed in the coatings with low Cu content. When the wear temperature was increased up to 400 °C, the wear rate increased sharply up to 10−6 mm3/N·m despite the formation of lubricious oxides of MoO3/CuMoO4 and V2O5. This could be due to the loss of nitrogen and pronounced oxidation at high temperatures, which led the wear mechanism to be transformed from mild oxidation wear to severe oxidation wear.

Catalytic oxidation of o-aminophenols and aromatic amines by mushroom tyrosinase.

Science.gov (United States)

Muñoz-Muñoz, Jose Luis; Garcia-Molina, Francisco; Garcia-Ruiz, Pedro Antonio; Varon, Ramon; Tudela, Jose; Rodriguez-Lopez, Jose N; Garcia-Canovas, Francisco

2011-12-01

The kinetics of tyrosinase acting on o-aminophenols and aromatic amines as substrates was studied. The catalytic constants of aromatic monoamines and o-diamines were both low, these results are consistent with our previous mechanism in which the slow step is the transfer of a proton by a hydroxyl to the peroxide in oxy-tyrosinase (Fenoll et al., Biochem. J. 380 (2004) 643-650). In the case of o-aminophenols, the hydroxyl group indirectly cooperates in the transfer of the proton and consequently the catalytic constants in the action of tyrosinase on these compounds are higher. In the case of aromatic monoamines, the Michaelis constants are of the same order of magnitude than for monophenols, which suggests that the monophenols bind better (higher binding constant) to the enzyme to facilitate the π-π interactions between the aromatic ring and a possible histidine of the active site. In the case of aromatic o-diamines, both the catalytic and Michaelis constants are low, the values of the catalytic constants being lower than those of the corresponding o-diphenols. The values of the Michaelis constants of the aromatic o-diamines are slightly lower than those of their corresponding o-diphenols, confirming that the aromatic o-diamines bind less well (lower binding constant) to the enzyme. Copyright © 2011 Elsevier B.V. All rights reserved.

Effect of Co3O4 and Co3O4/CeO2 infiltration on the catalytic and electro-catalytic activity of LSM15/CGO10 porous cells stacks for oxidation of propene

DEFF Research Database (Denmark)

Ippolito, Davide; Kammer Hansen, Kent

2015-01-01

The objective of this work was to study the effect of Co3O4 and Co3O4/CeO2 infiltration on the propene oxidation catalytic activity of a La0.85Sr0.15MnO3/Ce0.9Gd0.1O1.95 electrochemical porous cell stack (11 layers, 5 single cells in series). The effect of the infiltration of Co3O4 and Co3O4/CeO2...... on the electrochemical properties of the porous cell stack was also investigated by electrochemical impedance spectroscopy (EIS). Co3O4 and Co3O4/CeO2 exhibited high catalytic activity for propene oxidation. The increase of propene oxidation rate with +4 V (0.8 V/cell) polarization reached 10% for the Co3O4 infiltrated...... reactor and 48% of efficiency at 300 °C. The Co3O4/CeO2 co-infiltration decreased the reactor polarization resistance, while Co3O4 infiltration had negligible effect on reactor electrochemical performance. The beneficial effect of CeO2 on the electrode activity was attributed to the increased...

Co-Processing of Jatropha-Derived Bio-Oil with Petroleum Distillates over Mesoporous CoMo and NiMo Sulfide Catalysts

Directory of Open Access Journals (Sweden)

Shih-Yuan Chen

2018-02-01

Full Text Available The co-processing of an unconventional type of Jatropha bio-oil with petroleum distillates over mesoporous alumina-supported CoMo and NiMo sulfide catalysts (denoted CoMo/γ-Al2O3 and NiMo/γ-Al2O3 was studied. Either a stainless-steel high-pressure batch-type reactor or an up-flow fixed-bed reaction system was used under severe reaction conditions (330–350 °C and 5–7 MPa, similar to the conditions of the conventional diesel hydrodesulfurization (HDS process. To understand the catalytic performance of the mesoporous sulfide catalysts for co-processing, we prepared two series of oil feedstocks. First, model diesel oils, consisting of hydrocarbons and model molecules with various heteroatoms (sulfur, oxygen, and nitrogen were used for the study of the reaction mechanisms. Secondly, low-grade oil feedstocks, which were prepared by dissolving of an unconventional type of Jatropha bio-oil (ca. 10 wt % in the petroleum distillates, were used to study the practical application of the catalysts. Surface characterization by gas sorption, spectroscopy, and electron microscopy indicated that the CoMo/γ-Al2O3 sulfide catalyst, which has a larger number of acidic sites and coordinatively unsaturated sites (CUS on the mesoporous alumina framework, was associated with small Co-incorporated MoS2-like slabs with high stacking numbers and many active sites at the edges and corners. In contrast, the NiMo/γ-Al2O3 sulfide catalyst, which had a lower number of acidic sites and CUS on mesoporous alumina framework, was associated with large Ni-incorporated MoS2-like slabs with smaller stacking numbers, yielding more active sites at the brims and corresponding to high hydrogenation (HYD activity. Concerning the catalytic performance, the mesoporous CoMo/γ-Al2O3 sulfide catalyst with large CUS number was highly active for the conventional diesel HDS process; unfortunately, it was deactivated when oxygen- and nitrogen-containing model molecules or Jatropha bio

Impact of MoO3 interlayer on the energy level alignment of pentacene-C60 heterostructure.

Science.gov (United States)

Zou, Ye; Mao, Hongying; Meng, Qing; Zhu, Daoben

2016-02-28

Using in situ ultraviolet photoelectron spectroscopy, the electronic structure evolutions at the interface between pentacene and fullerene (C60), a classical organic donor-acceptor heterostructure in organic electronic devices, on indium-tin oxide (ITO) and MoO3 modified ITO substrates have been investigated. The insertion of a thin layer MoO3 has a significant impact on the interfacial energy level alignment of pentacene-C60 heterostructure. For the deposition of C60 on pentacene, the energy difference between the highest occupied molecular orbital of donor and the lowest unoccupied molecular orbital of acceptor (HOMO(D)-LUMO(A)) offset of C60/pentacene heterostructure increased from 0.86 eV to 1.54 eV after the insertion of a thin layer MoO3 on ITO. In the inverted heterostructrure where pentacene was deposited on C60, the HOMO(D)-LUMO(A) offset of pentacene/C60 heterostructure increased from 1.32 to 2.20 eV after MoO3 modification on ITO. The significant difference of HOMO(D)-LUMO(A) offset shows the feasibility to optimize organic electronic device performance through interfacial engineering approaches, such as the insertion of a thin layer high work function MoO3 films.

[Mo5VMo7VIO30(BPO4)2(O3P-Ph)6]5-: a phenyl-substituted molybdenum(V/VI) boro-phosphate polyoxometalate.

Science.gov (United States)

Sassoye, Capucine; Norton, Kieran; Sevov, Slavi C

2003-03-10

The title polyanion is the first hybrid borophosphate-phenylphosphonate polyoxometalate. It was structurally characterized as its imidazolium salt, (C(3)N(2)H(5))(5)[Mo(12)O(30)(BPO(4))(2)(O(3)P-Ph)(6)].H(2)O (monoclinic, P2(1)/c, a = 22.120(3) A, b = 13.042(2) A, and c = 32.632(4) A, beta = 101.293(3) degrees ), which was synthesized hydrothermally from imidazole, molybdenum oxide and metal, and boric, phosphoric, and phenylphosphonic acids. The anion is the second example of a new class of polyoxometalates that resemble Dawson anions but where the two pole caps of three edge-sharing MoO(6) octahedra in the latter are replaced by other units, in this case tetrahedral borate sharing corners with three phenylphosphonic groups, [(OB)(O(3)P-Ph)(3)]. The 12 molybdenum atoms forming the two equatorial belts of the cluster are of mixed-valence, five are Mo(V) and seven are Mo(VI), and the resulting five electrons are delocalized. Four of these electrons are paired according to the temperature dependence of the magnetic susceptibility. The new compound is soluble in a mixture of water and pyridine (in equal volumes) as well as in nitromethane, and the anions are intact in these solutions.

Theoretical investigation of lithium adsorption, diffusion and coverage on MX2 (M = Mo, W; X = O, S, Se, Te) monolayers

Science.gov (United States)

Ersan, F.; Ozaydin, H. D.; Gökoğlu, G.; Aktürk, E.

2017-12-01

It is important to improve the high-efficient anode materials for Li batteries, which require the large capacity, high stability and mobility. In this work, we present the adsorption and diffusion properties of lithium atom on MX2 (M = Mo, W; X = O, S, Se, Te) transition metal dichalcogenide structures using first principles calculations within density functional theory. All the MX2 systems considered are semiconductor in bare state with band gaps between 0.93 eV (MoO2) and 1.79 eV (WS2). They turn into metal upon single Li adsorption. Li atom is adsorbed on MoO2 and WO2 rather stronger than other systems. The energy barrier for diffusion of single Li on MX2 varies between 0.15 eV and 0.28 eV which are lower or comparable to that of graphene or silicene. Two Li atoms are preferably adsorbed on MX2 monolayer symmetrically at opposite sides with high adsorption energy. The increasing number of Li atoms does not remarkably affect the adsorption energy per Li atom. This can be attributed to that Li atoms do not accumulate on certain regions of the surface. The systems under investigation provide insights into exploring electronic properties which are rather adequate for possible applications in Li-ion batteries.

Effect of Ti content in the photo catalytic behavior of Fe/TiO2-SiO2 systems

International Nuclear Information System (INIS)

Leon C, A.; Portillo V, N.; Hernandez P, I.; May L, M.; Gonzalez R, L.; Luna P, R.; Suarez P, R.

2013-01-01

In this work we report the synthesis of Fe/TiO 2 -SiO 2 systems with different concentrations of TiO 2 in order to determine the influence of titanium content on the structural, textural, optical properties and their photo catalytic behavior. The materials were synthesized by the sol-gel method and their modification was carried out by incipient impregnation. All samples were characterized be means of X-ray diffraction, N 2 physisorption (Bet method), Dr-UV-Vis and Raman spectroscopy. The modifications of the structural and optical properties are discussed on the basis of long-range order reduction, suggesting the formation of highly dispersed TiO 2 species. On the other hand, it was observed that the energy of the optical band gap decreases by introducing Fe. On the basis of these phenomena, the photo catalytic activity was measured, employing the degradation of orange II azo dye as a model reaction. (Author)

Efficient, air-stable quantum dots light-emitting devices with MoO3 modifying the anode

International Nuclear Information System (INIS)

Meng, Xiangdong; Ji, Wenyu; Hua, Jie; Yu, Zhaoliang; Zhang, Yan; Li, Haibo; Zhao, Jialong

2013-01-01

In this work, we fabricated quantum dots light-emitting devices with hole-injection layer, molybdenum oxide (MoO 3 ) substituting for poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) which is hygroscopic and acidic and, therefore, a source of interface instability. A significant enhancement in luminance and current efficiency in MoO 3 -containing devices was observed. In addition, MoO 3 -containing devices were more stable in the air than those with PEDOT:PSS as the hole injection layer. The hole injection and transport of the devices were studied by the J–V characteristics of the hole-only devices. The excellent performance of the devices was principally a result of MoO 3 possessing lower injection barrier for the hole and better stability than PEDOT:PSS. -- Highlights: • We fabricated QD-LEDs with MoO 3 substituting for PEDOT:PSS as hole-injection layer. • A enhancement in luminance and efficiency in MoO 3 -containing device was observed. • The enhancement was originated from the stability and easy hole injection of MoO 3

Hydrothermal synthesis and crystal structure of a new molybdenum oxide compound with manganese-o-phen subunit: [Mn(o-phen)(H2O)MoO4]·H2O (o-phen=o-phenanthroline)

International Nuclear Information System (INIS)

Zhang Quanzheng; Lu Canzhong; Yang Wenbin; Chen Shumei; Yu Yaqin; He Xiang; Yan Ying; Liu Jiuhui; Xu Xinjiang; Xia Changkun; Wu Xiaoyuan; Chen Lijuan

2004-01-01

A new one-dimensional molybdenum oxide compound with manganese-o-phen subunit: [Mn(o-phen)(H 2 O)MoO 4 ]·H 2 O (1) (o-phen=o-phenanthroline) was synthesized by the hydrothermal reaction of Na 2 MoO 4 ·2H 2 O, MnSO 4 ·H 2 O, oxalic acid, o-phenanthroline (o-phen) and water. Its structure was determined by elemental analyses, ESR spectrum, TG analysis, IR spectrum and single-crystal X-ray diffraction. Compound 1 crystallizes in triclinic system, space group P-1 with a=7.0401(2) A, b=10.4498(2) A, c=10.5720(2) A, α=73.26(7) deg., β=83.34(8) deg., γ=77.33(9) deg., V=725.5089(0) A 3 , Z=2, and R 1 =0.0322 for 2337 observed reflections. Compound 1 exhibits one-dimensional chain structure. The chains are linked up via hydrogen bonding to 2D layers, which are further assembled through π-π stacking interactions to a 3D supermolecular structure

Optical properties of a new Bi{sub 38}Mo{sub 7}O{sub 78} semiconductor with fluorite-type δ-Bi{sub 2}O{sub 3} structure

Energy Technology Data Exchange (ETDEWEB)

Wang, Zuoshan; Bi, Shala; Wan, Yingpeng [State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123 (China); Huang, Pengjie [College of Textile and Clothing Engineering, Soochow University, Suzhou 215006 (China); Zheng, Min, E-mail: zhengmin@suda.edu.cn [College of Textile and Clothing Engineering, Soochow University, Suzhou 215006 (China)

2017-03-31

Highlights: • Bi{sub 38}Mo{sub 7}O{sub 78} semiconductor nanoparticles were synthesized by sol-gel method. • Bi{sub 38}Mo{sub 7}O{sub 78} keeps the structural characteristics of the patrimonial δ-Bi{sub 2}O{sub 3} structure. • Bi{sub 38}Mo{sub 7}O{sub 78} show an efficient optical absorption in visible light. • Photocatalytic property was markedly enhanced for Bi{sub 38}Mo{sub 7}O{sub 78} nanoparticles. • The mechanism of this photocatalysis system was proposed. - Abstract: Bi{sup 3+}-containing inorganic materials usually show rich optical and electronic properties due to the hybridization between 6s and 6p electronic components together with the lone pair in Bi{sup 3+} ions. In this work, a new semiconductor of bismuth molybdate Bi{sub 38}Mo{sub 7}O{sub 78} (19Bi{sub 2}O{sub 3}·7MoO{sub 3}) was synthesized by the sol-gel film coating and the following heat process. The samples developed into nanoparticles with average size of 40 nm. The phase formation was verified via the XRD Rietveld structural refinement. Orthorhombic Bi{sub 38}Mo{sub 7}O{sub 78} can be regarded to be derived from the cubic δ-phase Bi{sub 2}O{sub 3} structure. The microstructure was investigated by SEM, EDX, TEM, BET and XPS measurements. The UV-vis absorption spectra showed that the band gap of Bi{sub 38}Mo{sub 7}O{sub 78} (2.38 eV) was greatly narrowed in comparison with Bi{sub 2}O{sub 3} (2.6 eV). This enhances the efficient absorption of visible light. Meanwhile, the conduction band of is wider and shows more dispersion, which greatly benefits the mobility of the light-induced charges taking part in the photocatalytic reactions. Bi{sub 38}Mo{sub 7}O{sub 78} nanoparticles possess efficient activities on the photodegradation of methylene blue (MB) solutions under the excitation of visible-light. The photocatalysis activities and mechanisms were discussed on the crystal structure characteristics and the measurements such as photoluminescence, exciton lifetime and XPS results.

Experimental cross section for the {sup 152}Sm(n, γ){sup 153}Sm reaction at 0.0334 eV

Energy Technology Data Exchange (ETDEWEB)

Uddin, M. Shuza; Datta, Tapash Kumar; Hossain, Syed Mohammod; Zakaria, A.K.M.; Islam, Mohammad Amirul; Naher, Kamrun; Shariff, M. Asad; Yunus, S.M. [Atomic Energy Research Establishment, Dhaka (Bangladesh). Inst. of Nuclear Science and Technology; Afroze, Nasmin [Atomic Energy Research Establishment, Dhaka (Bangladesh). Inst. of Nuclear Science and Technology; Jahangirnagar Univ., Dhaka (Bangladesh). Dept. of Physics; Islam, S.M. Ajharul [Jahangirnagar Univ., Dhaka (Bangladesh). Dept. of Physics

2014-10-01

The neutron capture cross section for the {sup 152}Sm(n, γ){sup 153}Sm reaction at an energy of 0.0334 eV was measured for the first time using monochromatic neutrons of a powder diffractometer at the TRIGA Mark II nuclear reactor at Dhaka, Bangladesh. The {sup 197}Au(n, γ){sup 198}Au reaction was used to monitor the neutron beam intensity. The radioactivity of the products was determined via high resolution γ-ray spectrometry. The obtained cross section value is 184 ± 22b, which is consistent with both the ENDF/B-VII and TENDL-2012 data libraries. The measured value at 0.0334 eV and the previous data at 0.0536 eV confirm the reliability of the data in the above libraries. (orig.)

Non-enzymatic hydrogen peroxide biosensor based on rose-shaped FeMoO4 nanostructures produced by convenient microwave-hydrothermal method

International Nuclear Information System (INIS)

Liu, Hongying; Gu, Chunchuan; Li, Dujuan; Zhang, Mingzhen

2015-01-01

Graphical abstract: A non-enzymatic H 2 O 2 sensor with high selectivity and sensitivity based on rose-shaped FeMoO 4 synthesized by the convenient microwave-assisted hydrothermal method, was fabricated. - Highlights: • Rose-shaped FeMoO 4 is synthesized within 10 min via microwave-assisted hydrothermal approach. • Non-enzymatic hydrogen peroxide biosensor based on FeMoO 4 nanomaterials is fabricated. • The biosensor exhibits good performance. - Abstract: In this work, we demonstrated a simple, rapid and reliable microwave-assisted hydrothermal approach to synthesize the uniform rose-shaped FeMoO 4 within 10 min. The morphologies of the synthesized materials were characterized by X-ray powder diffraction and scanning electron microscopy. Moreover, a non-enzymatic amperometric sensor for the detection of hydrogen peroxide (H 2 O 2 ) was fabricated on the basis of the FeMoO 4 as electrocatalysis. The resulting FeMoO 4 exhibited high sensitivity and good stability for the detection of H 2 O 2 , which may be attributed to the rose-shaped structure of the material and the catalytic property of FeMoO 4 . Amperometric response showed that the modified electrode had a good response for H 2 O 2 with a linear range from 1 μM to 1.6 mM, a detection limit of 0.5 μM (S/N = 3), high selectivity and short response time. Additionally, good recoveries of analytes in real milk samples confirm the reliability of the prepared sensor in practical applications

Effect of Zr addition on structure and electrical properties of SmFeO3 prepared by solid state reaction method

Directory of Open Access Journals (Sweden)

Abdalla M. Abdalla

2017-12-01

Full Text Available Series of Sm1-xFe1-3xZr3xO3 (SFZO, where x = 0.0, 0.01, 0.02, 0.033, 0.05, 0.1 and 0.15, was synthesised by the solid state reaction method and sintered at 1500 °C in air. X-ray diffraction (XRD and scanning electron microscopy (SEM were used to investigate the structure of the materials. The XRD results indicated that the pure SmFeO3 and Sm0.99Fe0.97Zr0.03O3 samples are single phase materials with an orthorhombic symmetry and Pbnm space group. The increase of Zr content (x ≥ 0.02 causes a phase change from single to two-phase system with orthorhombic (Pbnm and fluorite symmetry (Fm3m. The microstructural analyses showed that the Zr4+ doping resulted in an increase of porosity in the sintered SFZO compared to SmFeO3 sample. The direct current (DC electrical conductivity at 850 °C in air was found to be 0.045 S/cm and 0.007 S/cm for Sm0.99Fe0.97Zr0.03O3 and SmFeO3, respectively, showing a significant enhancement compared to the pure SmFeO3.

Hydrothermal syntheses and characterization of two layered molybdenum selenites, Rb2(MoO3)3SeO3 and Tl2(MoO3)3SeO3

International Nuclear Information System (INIS)

Dussack, L.L.; Harrison, W.T.A.; Jacobson, A.J.

1996-01-01

The hydrothermal syntheses of Rb 2 (MoO 3 ) 3 SeO 3 , and Tl 2 (MoO 3 ) 3 SeO 3 are described. These compounds have structures built up from hexagonal-WO 3 -type sheets and are isostructural with the previously reported Cs 2 (MoO 3 ) 3 SeO 3 and (NH 4 ) 2 (MoO 3 ) 3 SeO 3 . Powder X-ray, thermogravimetric, and spectroscopic data are presented and discussed

2-Cyanopyrazine Prepared from 2-Methylpyrazine by Catalytic Ammoxidation on MoVPO Catalyst%MoVPO型催化剂上氨氧化合成2-氰基吡嗪

Institute of Scientific and Technical Information of China (English)

洪春; 李勇

2006-01-01

The mechanism of 2-cyanopyrazine prepared from 2-methylpyrazine (2-MP) by catalytic ammoxidation has been explained by the theory of appropriate structure of group. A new catalyst of MoVPO was developed. The effects of catalyst promoter phosphorus and supports were investigated. The catalyst containing P, V and Mo in molar ratio of 1.4 : 1: 0.02 and supported on activated alumina and prepared by impregnation method exhibits good activity and selectivity. Reaction factors such as reaction temperature, space velocity, feed composition and service life of catalyst were investigated. Optimum reaction conditions (the volume space velocity of 0.2h-1, the reaction temperature of 380 ℃ and molar ratio of 1: 7.8: 8 : 8 for 2-MP, water, oxygen and ammonia) were obtained. Selectivity of 93% and yield of 86% could be achieved under these conditions.

Interpretation of dc and ac conductivity of Ag2O–SeO2–MoO3 glass-nanocomposite-semiconductor

International Nuclear Information System (INIS)

Bhattacharya, Sanjib; Kundu, Ranadip; Das, Anindya Sundar; Roy, Debasish

2015-01-01

Highlights: • Polaron hopping. • Dc and ac conductivity. • Mott's model and Greave's model. • Ag 2 MoO 4 , Ag 2 Mo 2 O 7 and Ag 6 Mo 10 O 33 nanoparticles and SeO 3 and SeO 4 nanoclusters. • XRD and FESEM studies. - Abstract: A new type of semiconducting glass-nanocomposites 0.3Ag 2 O–0.7 (xMoO 3 –(1 − x) SeO 2 ) is prepared by melt-quenching route. The formation of Ag 2 MoO 4 , Ag 2 Mo 2 O 7 and Ag 6 Mo 10 O 33 nanoparticles and SeO 3 and SeO 4 nanoclusters in glass-nanocomposites has been confirmed from X-ray diffraction (XRD) and field emission scanning electron microscopic (FESEM) studies. Fourier transform infrared (FTIR) spectroscopy is employed to find out Se−O stretching vibration as well as stretching vibrations of Mo 2 O 7 2− ions. The dc conductivity of them is studied on the light of polaron hopping approach in a wide temperature range. At low temperatures, variable range hopping model (Mott's model) is employed to analyze the conductivity data. Greave's model is used to predict temperature dependent variable range hopping in the high temperature region. Frequency dependent ac conductivity is well explained on the basis of tunneling. I–V characteristics of the as-prepared samples have also been investigated

Multiple magnetic transitions in SmCoAsO

Directory of Open Access Journals (Sweden)

Yongliang Chen

2011-12-01

Full Text Available The magnetic properties of SmCoAsO have been investigated. Our results differ from early observations. Complicated magnetism consists of antiferromagnetic, ferromagnetic, ferrimagnetic and paramagnetic, even diamagnetism at low field has been observed. A metamagnetic transition was observed, resulting from a canting of the spins. The interaction between two Co sublattices with canted-structure might take responsibility for the multiple magnetic transitions. Electrical resistivity data indicate that SmCoAsO is metallic conductor with room temperature resistivity of 0.51669 mΩ-cm. Negative magnetoresistance effect suggests a significant suppression of spin-flip scattering by the applied magnetic field. The magnetic phase diagram has been established.

In situ DRIFTs investigation of the reaction mechanism over MnO{sub x}-MO{sub y}/Ce{sub 0.75}Zr{sub 0.25}O{sub 2} (M = Fe, Co, Ni, Cu) for the selective catalytic reduction of NO{sub x} with NH{sub 3}

Energy Technology Data Exchange (ETDEWEB)

Hu, Hang; Zha, Kaiwen; Li, Hongrui; Shi, Liyi; Zhang, Dengsong, E-mail: dszhang@shu.edu.cn

2016-11-30

Highlights: • MnO{sub x}-FeO{sub y}/Ce{sub 0.75}Zr{sub 0.25}O{sub 2} catalyst has a strong NO oxidation ability. • A high dispersion of active components is achieved on catalyst surface. • At high temperatures, bidentate nitrate is the common active species. • The addition of Fe can improve the reactivity of gaseous NO{sub 2} and bridged nitrates. - Abstract: A series of MnO{sub x}-MO{sub y}/Ce{sub 0.75}Zr{sub 0.25}O{sub 2} (M = Fe, Co, Ni, Cu) catalysts were synthesized by an impregnation method and used for selective catalytic reduction (SCR) of NO{sub x} with NH{sub 3}. The catalytic performances of various MnO{sub x}-MO{sub y}/Ce{sub 0.75}Zr{sub 0.25}O{sub 2} catalysts were studied. It was found that MnO{sub x}-FeO{sub y}/Ce{sub 0.75}Zr{sub 0.25}O{sub 2} catalyst showed excellent low-temperature activity and a broad temperature window. The catalysts were characterized by N{sub 2} adsorption/desorption, X-ray diffraction, X-ray photoelectron spectroscopy and in situ diffuse reflectance infrared transform spectroscopy (DRIFTS). Characterization of the catalyst confirmed the addition of iron oxide can enhance the NO oxidation ability of the catalyst which results in the outstanding low-temperature SCR activity. Meanwhile, iron oxides were well dispersed on catalyst surface which could avoid the agglomeration of active species, contributing to the strong interaction between active species and the support. More importantly, in situ DRIFTS results confirmed that bidentate nitrates are general active species on these catalysts, whereas the reactivity of gaseous NO{sub 2} and bridged nitrates got improved because of the addition of Fe.

SmBa2NbO6 Nanopowders, an Effective Percolation Network Medium for YBCO Superconductors

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S. Vidya

2013-01-01

Full Text Available The percolation behavior of superconductor-insulator composite, YBa2Cu3O7–δ, and nano SmBa2NbO2 synthesized by modified combustion technique was studied. Particle size of nano SmBa2NBO6 was determined using transmission electron microscopy. The chemical nonreactivity of nano SmBa2NbO6 with YBCO is evident from the X-Ray diffraction study which makes it a suitable nanoceramic substrate material for high temperature superconducting films. A systematic increase in the sintered density, approaching the optimum value of the insulating nanophase is clearly observed, as the vol.% of YBCO in the composite decreases. SEM micrograph showed uniform distribution of nanopowder among the large clusters of YBCO. The obtained percolation threshold is ~26 vol% of YBCO in the composite. All the composites below the threshold value showed TC(0~92 K even though the room resistivity increases with increase in vol.% of nano SmBa2NbO6. The values of critical exponents obtained matches well with the theoretically expected ones for an ideal superconductor-insulator system.

Facile synthesis of Sm-doped BiFeO{sub 3} nanoparticles for enhanced visible light photocatalytic performance

Energy Technology Data Exchange (ETDEWEB)

Hu, Zijun; Chen, Da, E-mail: dchen_80@hotmail.com; Wang, Sen; Zhang, Ning; Qin, Laishun, E-mail: qinlaishun@cjlu.edu.cn; Huang, Yuexiang

2017-06-15

Highlights: • Effective Sm doping into BiFeO{sub 3} nanoparticles was obtained by a facile sol-gel route. • Band gap of Sm-doped BiFeO{sub 3} nanoparticles was regulated by the dopant concentration. • Sm-doped BiFeO{sub 3} nanoparticles exhibited superior photocatalytic activities. • The possible photocatalytic mechanism of Sm-doped BiFeO{sub 3} nanospheres was discussed. - Abstract: In this work, the effect of Sm doping on the structural and photocatalytic properties of BiFeO{sub 3} (BFO) was investigated. A series of Sm doped BFO nanoparticles containing different Sm dopant contents (Bi{sub (1−x)}Sm{sub x}FeO{sub 3}, x = 0.00, 0.01, 0.03, 0.05, 0.07, 0.10) were synthesized via a simple sol-gel route. It was revealed that Sm{sup 3+} ions were successfully doped into BFO nanoparticles, and the band gap value was gradually decreased when increasing Sm dopant concentration. The photocatalytic activity of Sm-doped BFO photocatalyst was significantly affected by the Sm doping content. Compared to pure BFO, the Sm-doped BFO samples exhibited much higher photocatalytic activity. The improved photocatalytic activity of Sm-doped BFO could be attributed to the enhanced visible light absorption and the efficient separation of photogenerated electrons and holes derived from Sm dopant trapping level in the Sm-doped BFO samples. In addition, the possible photocatalytic mechanism of Sm-doped BFO photocatalyst was also proposed.

A facile route to large-scale synthesis MoO2 and MoO3 as electrode materials for high-performance supercapacitors

International Nuclear Information System (INIS)

Xuan, H.C.; Du, Y.W.; Zhang, Y.Q.; Xu, Y.K.; Li, H.; Han, P.D.; Wang, D.H.

2016-01-01

MoO 3 and MoO 2 materials have been successfully synthesized by thermal decomposition of ammonium paramolybdate in air and a sealed quartz tube, respectively. The microstructure of as-synthesized MoO 3 is composed of irregular lamellar plates with a plate thickness around 100 nm and MoO 2 has the larger grain size with lamellar plates connected with each other. A maximum specific capacitance of 318 F/g at 0.5 A/g is obtained for MoO 2 prepared in a closed environment. On the other hand, the sample MoO 3 exhibits excellent rate capacity with specific capacitances of 218, 209, 196, 188, 176, and 160 F/g at current densities of 0.5, 1, 2, 3, 4, and 5 A/g, respectively. These results pave the way to consider MoO 3 and MoO 2 as prospective materials for energy-storage applications. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Surface science models of CoMoS hydrodesulfurisation catalysts

Energy Technology Data Exchange (ETDEWEB)

De Jong, A.M.; De Beer, V.H.J.; Van Veen, J.A.R.; Niemantsverdriet, J.W. [Schuit Institute of Catalysis, Eindhoven University of Technology, Eindhoven (Netherlands)

1997-07-01

Characterization of supported catalysts with surface spectroscopic techniques is often limited due to restraints imposed by the support material. The use of flat conducting substrates as a model support offers a way to apply these techniques to their full potential. Such surface science models of silica and alumina supported CoMoS catalysts have been made by impregnating thin SiO{sub 2} and Al{sub 2}O{sub 3} films with a solution of nitrilotriacetic acid (NTA) complexes of cobalt and molybdenum. X-ray Photoelectron Spectroscopy (XPS) spectra indicate that the order in which cobalt and molybdenum transfer to the sulfided state is reversed with respect to oxidic Co and Mo systems prepared by conventional methods, implying that NTA complexation retards the sulfidation of cobalt to temperatures where MoS{sub 2} is already formed. Catalytic tests show that the CoMoS model catalysts exhibit activities for thiophene desulfurisation and product distributions similar to those of their high surface area counterparts. 25 refs.

Crystallographic and magnetic properties of nanocrystalline perovskite structure SmFeO3 orthoferrite

Science.gov (United States)

Kumar, Ashwini; Shen, Jingdong; Zhao, Huihui; Zhengjian, Qi; Li, Qi

2018-05-01

In this article, we present the structural and magnetic studies of pristine SmFeO3 nanocrystalline ceramic samples as sintered at temperature 850 °C and 1000 °C. X-ray powder diffraction data confirm the existence of single-phase nature with orthorhombic (Pbnm) structure of the samples. The SEM image reveals spherical particles with a size range of 60-130 nm for SFO-850 and SFO-1000 samples. X-ray absorption spectroscopy studies on Fe L3,2 and O K-edges of SmFeO3 sample revealed the homo-valence state of Fe in these materials. From magnetization studies it has been observed the materials exhibit ferromagnetic and antiferromagnetic (canted spin structure) sub-lattices, which results strong magnetic anisotropy in the system.

Improved photoelectrochemical performance of BiVO4/MoO3 heterostructure thin films

Science.gov (United States)

Kodan, Nisha; Mehta, B. R.

2018-05-01

Bismuth vanadate (BiVO4) and Molybdenum trioxide (MoO3) thin films have been prepared by RF sputtering technique. BiVO4 thin films were deposited on indium doped tin oxide (In: SnO2; ITO) substrates at room temperature and 80W applied rf power. The prepared BiVO4 thin films were further annealed at 450°C for 2 hours in air to obtain crystalline monoclinic phase and successively coated with MoO3 thin films deposited at 150W rf power and 400°C for 30 minutes. The effect of coupling BiVO4 and MoO3 on the structural, optical and photoelectrochemical (PEC) properties have been studied. Optical studies reveal that coupling of BiVO4 and MoO3 results in improvement of optical absorption in visible region of solar spectrum. PEC study shows approximate 3-fold and 38-fold increment in photocurrent values of BiVO4/MoO3 (0.38 mA/cm2) heterostructure thin film as compared to MoO3 (0.15 mA/cm2) and BiVO4 (10 µA/cm2) thin films at applied bias of 1 V vs Ag/AgCl in 0.5 M Na2SO4 (pH=7) electrolyte.

Catalisadores Ni/Al2O3 promovidos com molibdênio para a reação de reforma a vapor de metano Mo-Ni/AL2O3 catalysts for the methane steam reforming reaction

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Silvia Sálua Maluf

2003-03-01

Full Text Available Mo-promoted Ni/Al2O3 catalysts for the methane steam reforming reaction were studied in this work. The Ni/Al2O3 catalysts were prepared by precipitation and molibdenum was added by impregnation up to 2%wt. The solids were tested using a micro-reactor under two H2Ov/C conditions and were characterized by ICP-OES, XRD, N2 adsoption, H2 chemisorption and TPR. NiO and NiAl2O4 phases were observed and the metallic area decreased with the increase of the Mo content. From the catalytic tests high stability was verified for H2Ov/C=4.0. On the other hand, only the catalyst containing 0,05% Mo stayed stable during 30 hours of the test at H2Ov/C=2.0.

Crystal structure of molybdenyl tetrapolyphosphate (MoO)2P4O13

International Nuclear Information System (INIS)

Minacheva, L.Kh.; Antsishkina, A.S.; Lavrov, A.V.; Sakharova, V.G.; Nikolaev, V.P.; Poraj-Koshits, M.A.

1979-01-01

The structure of crystals of molybdenyl tetrapolyphosphate [MoO] 2 P 4 O 13 has been determined. The substance is crystallized in the monoclinic syngony with the following parameters of the elementary cell: a=8.288 (2); b=10.690 (3); c=19.529 (5) A; γ=106.7 (3) deg. The structural units are molybdenyl groups MoO(3 + ) and polyphosphate anions P 4 O 13 (6 - ) that are composed of four PO 4 tetrahedrons whose apexes are connected in series. Three atoms of phasphate anion form the ''internal'' P-O-P bridges, while the remaining oxygen atoms, the ''external'' P-O-Mo bridges. The optimum temperature of crystals synthesis is 450 - 460 deg C. A mixture of phase of MoO 2 P 4 O 13 and Mo(PO 3 ) 3 is obtained as temperature is raised up to 600 deg C. Consequently, the stepwise dissociation of molybdenyl ions with the splitting off of oxygen and gradual reduction in the degree of molybdenum oxidation (MoO 2 ) 2+ → (MoO) 3+ → Mo 3+ occurs in the solution

Layered SmBaCuCoO5+δ and SmBaCuFeO5+δ perovskite oxides as cathode materials for proton-conducting SOFCs

International Nuclear Information System (INIS)

Nian Qiong; Zhao Ling; He Beibei; Lin Bin; Peng Ranran; Meng Guangyao; Liu Xingqin

2010-01-01

A dense BaCe 0.8 Sm 0.2 O 5+δ (BCS) electrolyte was fabricated on a porous anode by in situ drop-coating to develop a simple and cost-effective route to fabricate proton-conducting solid oxide fuel cells (SOFCs). Layered perovskite-structure oxides SmBaCuCoO 5+δ (SBCC) and SmBaCuFeO 5+δ (SBCF) were prepared and the electrical conductivity, the thermal expansion coefficient and electrochemical performance were investigated as potential cathode materials for proton-conducting SOFCs. Thermal expansion coefficients of SBCC and SBCF were suitable for BCS electrolyte and the electrical conductivity of the SBCC is higher than that of the SBCF. The maximum power density of 449 mW cm 2 and 333 mW cm 2 at 700 o C were obtained for the SBCC/BCS/NiO-BCS and SBCF/BCS/NiO-BCS cells, respectively. The interfacial polarization resistances for SBCC and SBCF cathode are as low as 0.137 Ω cm -2 and 0.196 Ω cm -2 at 700 o C, respectively. The results indicate that the SBCC and SBCF are promising cathode materials for proton-conducting SOFCs.

Al atom on MoO3(010) surface: adsorption and penetration using density functional theory.

Science.gov (United States)

Wu, Hong-Zhang; Bandaru, Sateesh; Wang, Da; Liu, Jin; Lau, Woon Ming; Wang, Zhenling; Li, Li-Li

2016-03-14

Interfacial issues, such as the interfacial structure and the interdiffusion of atoms at the interface, are fundamental to the understanding of the ignition and reaction mechanisms of nanothermites. This study employs first-principle density functional theory to model Al/MoO3 by placing an Al adatom onto a unit cell of a MoO3(010) slab, and to probe the initiation of interfacial interactions of Al/MoO3 nanothermite by tracking the adsorption and subsurface-penetration of the Al adatom. The calculations show that the Al adatom can spontaneously go through the topmost atomic plane (TAP) of MoO3(010) and reach the 4-fold hollow adsorption-site located below the TAP, with this subsurface adsorption configuration being the most preferred one among all plausible adsorption configurations. Two other plausible configurations place the Al adatom at two bridge sites located above the TAP of MoO3(010) but the Al adatom can easily penetrate below this TAP to a relatively more stable adsorption configuration, with a small energy barrier of merely 0.2 eV. The evidence of subsurface penetration of Al implies that Al/MoO3 likely has an interface with intermixing of Al, Mo and O atoms. These results provide new insights on the interfacial interactions of Al/MoO3 and the ignition/combustion mechanisms of Al/MoO3 nanothermites.

Studies of scintillation properties of CaMoO{sub 4} at millikelvin temperatures

Energy Technology Data Exchange (ETDEWEB)

Zhang, X.; Lin, J.; Kraus, H. [Department of Physics, University of Oxford, Keble Rd., Oxford OX1 3RH (United Kingdom); Mikhailik, V. B., E-mail: vmikhai@hotmail.com [Diamond Light Source, Harwell Science Campus, Didcot OX11 0DE (United Kingdom)

2015-06-15

Application of CaMoO{sub 4} as a scintillation target in cryogenic rare event searches relies on the understanding of scintillation properties of the material at the temperatures at which these detectors operate. We devised and implemented a detection module with a low-temperature photomultiplier from Hamamatsu (model R8520-06) powered by a Cockcroft-Walton generator. The detector module containing the CaMoO{sub 4} crystal was placed in a {sup 3}He/{sup 4}He dilution refrigerator and used to measure scintillation characteristics of CaMoO{sub 4} in the millikelvin temperature range. At the lowest temperature achieved, the energy resolution of CaMoO{sub 4} for 122 keV γ from a {sup 57}Co source is found to be 30%, and the fast and slow decay constants are 40.6 ± 0.8 μs and 3410 ± 50 μs, respectively. The temperature variation of the CaMoO{sub 4} decay kinetics is discussed in terms of a three-level model of the emission center.

Measurement and Estimation of the 99Mo Production Yield by 100Mo(n,2n)99Mo

Science.gov (United States)

Minato, Futoshi; Tsukada, Kazuaki; Sato, Nozomi; Watanabe, Satoshi; Saeki, Hideya; Kawabata, Masako; Hashimoto, Shintaro; Nagai, Yasuki

2017-11-01

We, for the first time, measured the yield of 99Mo, the mother nuclide of 99mTc used in nuclear medicine diagnostic procedures, produced by the 100Mo(n,2n)99Mo reaction with accelerator neutrons. The neutrons with a continuous energy spectrum from the thermal energy up to about 40 MeV were provided by the C(d,n) reaction with 40 MeV deuteron beams. It was proved that the 99Mo yield agrees with that estimated by using the latest data on neutrons from the C(d,n) reaction and the evaluated cross section of the 100Mo(n,2n)99Mo reaction given in the Japanese Evaluated Nuclear Data Library. On the basis of the agreement, a systematic calculation was carried out to search for an optimum condition that enables us to produce as much 99Mo as possible with a good 99Mo/100Mo value from an economical point of view. The calculated 99Mo yield from a 150 g 100MoO3 sample indicated that about 30% of the demand for 99Mo in Japan can be met with a single accelerator capable of 40 MeV, 2 mA deuteron beams. Here, by referring to an existing 18F-fluorodeoxyglucose (FDG) distribution system we assumed that 99mTc radiopharmaceuticals formed after separating 99mTc from 99Mo can be delivered to hospitals from a radiopharmaceutical company within 6 h. The elution of 99mTc from 99Mo twice a day would meet about 50% of the demand for 99Mo.

Thermochemical studies on complex of [Sm(o-NBA)_3phen]_2

Institute of Scientific and Technical Information of China (English)

肖圣雄; 张建军; 李旭; 李强国; 任宁; 李环

2010-01-01

A ternary complex [Sm(o-NBA)3phen]2 (o-NBA: o-Nitrobenzoate; phen: 1,10-phenanthroline) was synthesized and characterized by elemental analysis, IR, molar conductance, and thermogravimetric analysis. The dissolution enthalpies of SmCl3·6H2O(s), o-HNBA(s) and phen·H2O(s) in mixed solvent (VHCl :VDMF :VDMSO=2:2:1) were determined by calorimetry at 298.15 K. The enthalpy change of the reaction was determined to be rHmΔθ=252.49±1.60 kJ/mol. Using the relevant data in the literature and a thermochemical recycle ...

Influence of Sm{sup 3+} substitution on the mutiferroic effect in NdCrTiO{sub 5}

Energy Technology Data Exchange (ETDEWEB)

Qian, X.L., E-mail: xiaolongqian@shu.edu.cn [Materials Genome Institute, Shanghai University, Shanghai 200444 (China); Department of Physics, Shanghai University, Shanghai 200444 (China); Fang, Y.F.; Kang, J.; Cao, S.X. [Materials Genome Institute, Shanghai University, Shanghai 200444 (China); Department of Physics, Shanghai University, Shanghai 200444 (China); Zhang, J.C., E-mail: jczhang@shu.edu.cn [Materials Genome Institute, Shanghai University, Shanghai 200444 (China); Department of Physics, Shanghai University, Shanghai 200444 (China)

2016-08-15

The effects of Sm{sup 3+} substitution on the magnetic and electric properties of NdCrTiO{sub 5} are investigated by magnetization and polarization measurements. X-ray diffraction patterns confirm that our samples are single phase with an orthorhombic crystal structure in the space group of Pbam. The DC magnetization study at an external field of 0.1 T reveals the variation of the anti-ferromagnetic transition temperature. The disappearance of the ferroelectricity–paraelectricity phase transition in Nd{sub 0.5}Sm{sub 0.5}CrTiO{sub 5} indicates the suppression on the linear magnetoelectric coupling by Sm{sup 3+}. The disparate 3d−4f interactions between Sm and Cr potentially affect the mutiferroic effect in this system.

Vanadium(V-Substitution Reactions of Wells–Dawson-Type Polyoxometalates: From [X2M18O62]6− (X = P, As; M = Mo, W to [X2VM17O62]7−

Directory of Open Access Journals (Sweden)

Tadaharu Ueda

2015-07-01

Full Text Available The formation processes of V(V-substituted polyoxometalates with the Wells–Dawson-type structure were studied by cyclic voltammetry and by 31P NMR and Raman spectroscopy. Generally, the vanadium-substituted heteropolytungstates, [P2VW17O62]7− and [As2VW17O62]7−, were prepared by mixing equimolar amounts of the corresponding lacunary species—[P2W17O61]10− and [As2W17O61]10−—and vanadate. According to the results of various measurements in the present study, the tungsten site in the framework of [P2W18O62]6− and [As2W18O62]6− without defect sites could be substituted with V(V to form the [P2VW17O62]7− and [As2VW17O62]7−, respectively. The order in which the reagents were mixed was observed to be the key factor for the formation of Dawson-type V(V-substituted polyoxometalates. Even when the concentration of each reagent was identical, the final products differed depending on the order of their addition to the reaction mixture. Unlike Wells–Dawson-type heteropolytungstates, the molybdenum sites in the framework of [P2Mo18O62]6− and [As2Mo18O62]6− were substituted with V(V, but formed Keggin-type [PVMo11O40]4− and [AsVMo11O40]4− instead of [P2VMo17O62]7− and [As2VMo17O62]7−, respectively, even though a variety of reaction conditions were used. The formation constant of the [PVMo11O40]4− and [AsVMo11O40]4− was hypothesized to be substantially greater than that of the [P2VMo17O62]7− and [As2VMo17O62]7−.

Synthesis and characterization of multiferroic Sm-doped BiFeO{sub 3} nanopowders and their bulk dielectric properties

Energy Technology Data Exchange (ETDEWEB)

Yotburut, Benjaporn [School of Physics, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima 30000 (Thailand); Thongbai, Prasit [Department of Physics, Faculty of Science, Khon Kaen University, Khon Kaen 40002 (Thailand); Yamwong, Teerapon [National Metals and Materials Technology Center (MTEC), Thailand Science Park, Pathumthani 12120 (Thailand); Maensiri, Santi, E-mail: santimaensiri@g.sut.ac.th [School of Physics, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima 30000 (Thailand); SUT Center of Excellence on Advanced Functional Materials, Suranaree University of Technology, Nakhon Ratchasima 30000 (Thailand)

2017-09-01

Highlights: • Bi{sub 1−x}Sm{sub x}FeO{sub 3} nanopowders were prepared by a simple co-precipitation method. • The prepared samples were well characterized by XRD, TEM, SEM, and XAS. • The XANES spectra identified the valence state of Fe ion in all nanopowders as 3+. • Increasing in applied dc bias voltage from 0 to 20 V causes a decrease in the dielectric constant. • The relaxation activation energy of a LFR is larger than that of a HFR. - Abstract: Multiferroic Bi{sub 1−x}Sm{sub x}FeO{sub 3} (x = 0, 0.05, 0.1, 0.2, and 0.3) nanopowders with particle sizes of 69–22.6 nm were prepared by a simple co-precipitation method. The structure and morphology of the samples were examined using X-ray diffraction (XRD) and scanning electron microscopy (SEM). The XRD patterns confirmed the phase transition from rhombohedral to orthorhombic phases. The results of X-ray absorption spectroscopy (XAS) data indicate that the oxidation state of Fe in the sample was Fe{sup 3+}. The results of magnetic properties revealed the enhancement of weak ferromagnetic property with increasing Sm doping in BFO nanopowders. SEM images revealed that the average grain size decreased with an increase in Sm concentration. Undoped BFO ceramics exhibited a high dielectric constant ε′ ∼1.1 × 10{sup 4} and a low loss tangent of tan δ ∼0.5 at room temperature for 1 kHz. The room temperature dielectric constant decreased with increasing concentration of Sm doping and the dielectric relaxation peaks were observed at x ≤ 0.1. The dielectric relaxation peaks which were observed at all frequency ranges were x ≤ 0.1 samples which were attributed to Maxwell-Wagner relaxation. As the temperature increased, great increases in dielectric permittivity were observed in all the Bi{sub 1−x}Sm{sub x}FeO{sub 3} samples. The effects of grain boundaries on the dielectric properties of Sm-doped BFO ceramics were investigated by measuring the dielectric responds in the frequencies of 100 Hz–1

Catalytic Ethanol Dehydration to Ethylene over Nanocrystalline χ- and γ-Al2O3 Catalysts.

Science.gov (United States)

Janlamool, Jakrapan; Jongsomjit, Bunjerd

2017-01-01

The study is aimed to investigate the combination of nanocrystalline γ- and χ- alumina that displays the attractive chemical and physical properties for the catalytic dehydration of ethanol. The correlation between the acid density and ethanol conversion was observed. The high acid density apparently results in high catalytic activity, especially for the equally mixed γ- and χ- phase alumina (G50C50). In order to obtain a better understanding on how different catalysts would affect the ethylene yield, one of the most powerful techniques such as X-ray photoelectron spectroscopy (XPS) was performed. Hence, the different O 1s surface atoms can be identified and divided into three types including lattice oxygen (O, 530.7 eV), surface hydroxyl (OH, 532.1 eV) and lattice water (H 2 O, 532.9 eV). It was remarkably found that the large amount of O 1s surface atoms in lattice water can result in increased ethylene yield. In summary, the appearance of metastable χ-alumina structure exhibited better catalytic activity and ethylene yield than γ- alumina. Thus, the introduction of metastable χ- alumina structure into γ- alumina enhanced catalytic activity and ethylene yield. As the result, it was found that the G50C50 catalyst exhibits the ethylene yield (80%) at the lowest reaction temperature ca. 250°C among other catalysts.

Absorption Spectra of BaF2 Sm2O3, Sm, Gd, and Ho Plasmas

Science.gov (United States)

Martin, Michael; Bastiani-Ceccotti, Serena

2009-11-01

Knowledge of the opacities of high Z element plasmas is important in indirect drive ICF and the study of stellar evolution. There are few experimental measurements of this quantity, and its theoretical determination is difficult due to the number of possible bound electron configurations. This study aims to better the theoretical understanding of this parameter by looking at the 3d-4f transitions of BaF2, Sm2O3, Sm, Gd, and Ho plasmas at the LULI2000 facility. The plasmas are produced by radiative heating and are cold, 15 -- 40 eV, and relatively dense, ˜ .01gm/cm^3 A plasma is produced by a .5 ns laser pulse irradiating a gold hohlraum and then probed by an x-ray source created by a gold foil irradiated by a 10 ps laser pulse. The transmission is found with simultaneous source and absorption measurements by an x-ray spectrometer in the 8 - 20 å range We will compare the results with statistical atomic structure codes. From this experiment we will gain further insight into the spectral broadening of neighboring Z elements due to changing plasma temperature and into mixture thermodynamics. This is a first step towards an experimental study of astrophysical domains.

Study on preparation of SnO2-TiO2/Nano-graphite composite anode and electro-catalytic degradation of ceftriaxone sodium.

Science.gov (United States)

Guo, Xiaolei; Wan, Jiafeng; Yu, Xiujuan; Lin, Yuhui

2016-12-01

In order to improve the electro-catalytic activity and catalytic reaction rate of graphite-like material, Tin dioxide-Titanium dioxide/Nano-graphite (SnO 2 -TiO 2 /Nano-G) composite was synthesized by a sol-gel method and SnO 2 -TiO 2 /Nano-G electrode was prepared in hot-press approach. The composite was characterized by X-ray photoelectron spectroscopy, fourier transform infrared, Raman, N 2 adsorption-desorption, scanning electrons microscopy, transmission electron microscopy and X-ray diffraction. The electrochemical performance of the SnO 2 -TiO 2 /Nano-G anode electrode was investigated via cyclic voltammetry and electrochemical impedance spectroscopy. The electro-catalytic performance was evaluated by the degradation of ceftriaxone sodium and the yield of ·OH radicals in the reaction system. The results demonstrated that TiO 2 , SnO 2 and Nano-G were composited successfully, and TiO 2 and SnO 2 particles dispersed on the surface and interlamination of the Nano-G uniformly. The specific surface area of SnO 2 modified anode was higher than that of TiO 2 /Nano-G anode and the degradation rate of ceftriaxone sodium within 120 min on SnO 2 -TiO 2 /Nano-G electrode was 98.7% at applied bias of 2.0 V. The highly efficient electro-chemical property of SnO 2 -TiO 2 /Nano-G electrode was attributed to the admirable conductive property of the Nano-G and SnO 2 -TiO 2 /Nano-G electrode. Moreover, the contribution of reactive species ·OH was detected, indicating the considerable electro-catalytic activity of SnO 2 -TiO 2 /Nano-G electrode. Copyright © 2016 Elsevier Ltd. All rights reserved.

Surface chemistry and catalytic properties of VOX/Ti-MCM-41 catalysts for dibenzothiophene oxidation in a biphasic system

International Nuclear Information System (INIS)

González, J.; Chen, L.F.; Wang, J.A.; Manríquez, Ma.; Limas, R.; Schachat, P.; Navarrete, J.; Contreras, J.L.

2016-01-01

Highlights: • Oxidative desulfurization of model diesel was tested in a biphasic system. • ODS activity was proportional to the V 5+ /(V 4+ + V 5+ ) values of the catalysts. • Lewis acidity was related to vanadium content and catalytic activity. • 99.9% DBT was oxidized using 25%V 2 O 5 /Ti-MCM-41 at 60 °C within 60 min. - Abstract: A series of vanadium oxide supported on Ti-MCM-41 catalysts was synthesized via the incipient impregnation method by varying the vanadia loading from 5 wt% to 10, 15, 20 and 25 wt%. These catalysts were characterized by a variety of advanced techniques for investigating their crystalline structure, textural properties, and surface chemistry information including surface acidity, reducibility, vanadium oxidation states, and morphological features. The catalytic activities of the catalysts were evaluated in a biphasic reaction system for oxidative desulfurization (ODS) of a model diesel containing 300 ppm of dibenzothiophene (DBT) where acetonitrile was used as extraction solvent and H 2 O 2 as oxidant. ODS activity was found to be proportional to the V 5+ /(V 4+ + V 5+ ) values of the catalysts, indicating that the surface vanadium pentoxide (V 2 O 5 ) was the active phase. Reaction temperature would influence significantly the ODS efficiency; high temperature, i.e., 80 °C, would lead to low ODS reaction due to the partial decomposition of oxidant. All the catalysts contained both Lewis and Brønsted acid sites but the former was predominant. The catalysts with low vanadia loading (5 or 10 wt%V 2 O 5 ) had many Lewis acid sites and could strongly adsorb DBT molecule via the electron donation/acceptance action which resulted in an inhibition for the reaction of DBT with the surface peroxometallic species. The catalyst with high vanadia loading (25wt%V 2 O 5 /Ti-MCM-41) showed the highest catalytic activity and could remove 99.9% of DBT at 60 °C within 60 min.

Thermal Behaviour of Sm0.5 R 0.5FeO3 (R = Pr, Nd) Probed by High-Resolution X-ray Synchrotron Powder Diffraction.

Science.gov (United States)