Laves-phase evolution during aging in 9Cr-1.8W-0.5Mo-VNb steel for USC power plants

Energy Technology Data Exchange (ETDEWEB)

Wang, Xue, E-mail: wangxue2011@whu.edu.cn [School of Power and Mechanics, Wuhan University, Wuhan 430072 (China); Xu, Qiang [School of Computing and Engineering, The University of Huddersfield, Huddersfield HD1 3DH, England (United Kingdom); Yu, Shu-min; Hu, Lei [School of Power and Mechanics, Wuhan University, Wuhan 430072 (China); Liu, Hong [DongFang Boiler Group Co.,Ltd., Zigong 643001 (China); Ren, Yao-yao [School of Power and Mechanics, Wuhan University, Wuhan 430072 (China)

2015-08-01

Long term precipitation and coarsening of Laves-phase in tungsten strengthened 9% Cr steel under thermal aging at 923 K was investigated and reported in this paper. It experimentally measured the evolution of mean particle size, the number density, the volume fraction of Laves-phase precipitates, the partition coefficients of W and Mo in the matrix, as well as the change of hardness. Its main conclusions were: 1) Laves-phase nucleates and grows rapidly on grain boundaries and lath boundaries within the first 1500 h of aging time; 2) The two stages characteristics and kinetics of Laves-phase nucleation and growth which were determined experimentally; 3) The coarsening of Laves-phase is much faster than that of M{sub 23}C{sub 6} carbides; 4) The precipitation of Laves-phase produces a pronounced matrix depletion of W and Mo atoms; and 5) The precipitated Laves-phase gives rise to weaker precipitation strengthening in comparison with M{sub 23}C{sub 6} carbides, and causes the loss of hardness due to the depletion of Mo and W from the solid solution. This paper contributes to the knowledge of kinetics of Laves-phase precipitation and coarsening, providing the essential information for comparative investigation of creep damage mechanisms. This paper also contributes to the understanding the creep damage broadly. - Highlights: • The characteristics of precipitation and coarsening of Laves-phase were determined. • The matrix depletion of W and Mo due to Laves-phase precipitation was quantified. • The effect of precipitated Laves-phase on the hardness was evaluated.

High-pressure modifications of CaZn2, SrZn2, SrAl2, and BaAl2: Implications for Laves phase structural trends

International Nuclear Information System (INIS)

Kal, Subhadeep; Stoyanov, Emil; Belieres, Jean-Philippe; Groy, Thomas L.; Norrestam, Rolf; Haeussermann, Ulrich

2008-01-01

High-pressure forms of intermetallic compounds with the composition CaZn 2 , SrZn 2 , SrAl 2 , and BaAl 2 were synthesized from CeCu 2 -type precursors (CaZn 2 , SrZn 2 , SrAl 2 ) and Ba 21 Al 40 by multi-anvil techniques and investigated by X-ray powder diffraction (SrAl 2 and BaAl 2 ), X-ray single-crystal diffraction (CaZn 2 ), and electron microscopy (SrZn 2 ). Their structures correspond to that of Laves phases. Whereas the dialuminides crystallize in the cubic MgCu 2 (C15) structure, the dizincides adopt the hexagonal MgZn 2 (C14) structure. This trend is in agreement with the structural relationship displayed by sp bonded Laves phase systems at ambient conditions. - Graphical abstract: CeCu 2 -type polar intermetallics can be transformed to Laves phases upon simultaneous application of pressure and temperature. The observed structures are controlled by the valence electron concentration

Lave phase precipitation in Nb- and Ti-based alloys

International Nuclear Information System (INIS)

Tewari, R.; Vishwanadh, B.; Dey, G.K.

2010-01-01

In multicomponent Nb-based alloys system, which are potential candidate materials for high temperature applications, the presence of Laves phase was noticed along with the silicides in equilibrium with the soft β-matrix. In Ti-Cr alloys, which show a tendency for inverse melting, the formation of the phase was noticed in the β matrix upon aging. The Laves phase being topologically closed pack structure appears to have strong tendency for the formation provided the criterion of atomic size factor is met

Synthesis, characterization and magnetic properties of selected Laves and MAX phases

International Nuclear Information System (INIS)

Hamm, Christin Maria

2017-01-01

In this work the rare-earth free Laves phases Ti 2 M 3 Si with M = Mn, Fe, Co, Ni were synthesized by microwave heating and were structurally and magnetically characterized. Furthermore, the solid solution Ti 2 (Co 1-x Fe x ) 3 Si was synthesized by arc melting and spark plasma sintering, as well as their magnetic behavior was studied. In addition to the Laves phases, the focus was on the synthesis and characterization of aluminum-based MAX phases. For the first time the ternary carbides were prepared by microwave heating. The phase-pure representation of MAX phases was particularly challenging for synthetic solid-state chemistry. The susceptor-assisted microwave heating allows the synthesis of high-quality samples, which was shown in this work on M 2 AlC (M = Ti, V, Cr) and V 4 AlC 3 . Furthermore, for the first time, the doping of these materials with Mn and Fe was successful. In addition to the structural characterization of the new phases, the microstructure and magnetic properties are discussed in this work. Using these doped compounds as well as the compound V 4 AlC 3 , it has been shown that field-activated synthesis, particularly susceptor-assisted microwave heating, are a very good synthesis method for compounds which are hard or sometimes not synthesized by conventional methods.

Role of copper on Laves phase morphology in 9-12%Cr steels

DEFF Research Database (Denmark)

Danielsen, Hilmar Kjartansson; Liu, Fang

2017-01-01

In this work the Laves phase was found to appear in two different morphologies, namely granular shapes and in an elongated shape. No difference in crystallography could be detected between these morphologies. The Laves phase was only observed in its elongated form in Cu-containing steels, where i...

Clean Grain Boundary Found in C14/Body-Center-Cubic Multi-Phase Metal Hydride Alloys

Directory of Open Access Journals (Sweden)

Hao-Ting Shen

2016-06-01

Full Text Available The grain boundaries of three Laves phase-related body-center-cubic (bcc solid-solution, metal hydride (MH alloys with different phase abundances were closely examined by scanning electron microscopy (SEM, transmission electron microscopy (TEM, and more importantly, electron backscatter diffraction (EBSD techniques. By using EBSD, we were able to identify the alignment of the crystallographic orientations of the three major phases in the alloys (C14, bcc, and B2 structures. This finding confirms the presence of crystallographically sharp interfaces between neighboring phases, which is a basic assumption for synergetic effects in a multi-phase MH system.

Electron crystallography applied to the structure determination of Nb(Cu,Al,X) Laves phases.

Science.gov (United States)

Gigla, M; Lelatko, J; Krzelowski, M; Morawiec, H

2006-09-01

The presence of primary precipitates of the Laves phases considerably improves the mechanical properties and the resistance to thermal degradation of the high-temperature shape memory Cu-Al-Nb alloys. The structure analysis of the Laves phases was carried out on particles contained in the ternary and quaternary alloys as well on synthesized compounds related to the composition of the Nb(Cu,Al,X)(2) phase, where X = Ni, Co, Cr, Ti and Zr. The precise structure determination of the Laves phases was carried out by the electron crystallography method using the CRISP software.

Precipitation behavior of Laves phase and its effect on toughness of 9Cr-2Mo ferritic-martensitic steel

International Nuclear Information System (INIS)

Hosoi, Y.; Wade, N.; Kunimitsu, S.; Urita, T.

1986-01-01

This study clarified the relationship between the toughness of a 9Cr-2Mo dual phase steel and precipitates formed during aging, with special attention to the Laves phase (Fe 2 Mo). The ductile-brittle transition temperature (DBTT) is increased and the upper shelf energy decreased when the Laves phase begins to precipitate during aging. Electron microscopy and X-ray diffraction indicate that elimination of Si in the steel reduces the precipitation of the Laves phase and results in maintaining good toughness. It is also noted that the toughness of the steel is controlled by the total amount of precipitates (Laves + carbides) in the aging at 873 K for more than 3.6x10 3 ks. A time-temperature-precipitation diagram for the Laves phase is established and it clearly shows that the precipitation of the Laves phase is markedly retarded by the decrease of Si content. In Si-free steel, no Laves phase is observed in the temperature and time range investigated. (orig.)

The effect of hot pressing time on the microstructure and properties of Laves phase NbCr{sub 2} alloys

Energy Technology Data Exchange (ETDEWEB)

Xiao, X. [College of Electromechanical Engineering, Nanjing University of Aeronautical and Astronautics, Nanjing 210016 (China); School of Materials Science and Engineering, Nanchang Institute of Aeronautical Technology, Nanchang 330063 (China); Lu, S.Q. [School of Materials Science and Engineering, Nanchang Institute of Aeronautical Technology, Nanchang 330063 (China)], E-mail: niatlusq@126.com; Hu, P.; Huang, M.G.; Nie, X.W. [School of Materials Science and Engineering, Nanchang Institute of Aeronautical Technology, Nanchang 330063 (China); Fu, M.W. [Department of Mechanical Engineering, Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong (China)

2008-06-25

The microstructure and properties were investigated on the Laves phase NbCr{sub 2} alloys prepared through 20 h mechanical alloying of niobium and chromium powders and subsequent hot pressing at 1250 deg. C for different time. The results indicate that the Laves phase NbCr{sub 2} alloy with homogeneous microstructure and fine grains and high relative density is obtained. With the increase of hot pressing time, the density, grain size and Vickers hardness increase, the fracture toughness, however, decreases gradually. The alloy fabricated by hot pressing at 1250 deg. C for 30 min has the best overall properties. Its average grain size reaches about 248 nm, the relative density is 97.8% and the fracture toughness at room temperature is more than 4.7 MPa m{sup 1/2}. Compared with the Laves phase NbCr{sub 2} alloy prepared by arc-melting, which has the fracture toughness of 1.2 MPa m{sup 1/2}, the fracture toughness in this research is increased significantly.

Ternary rhombohedral Laves phases RE_2Rh_3Ga (RE = Y, La-Nd, Sm, Gd-Er)

International Nuclear Information System (INIS)

Seidel, Stefan; Benndorf, Christopher; Heletta, Lukas; Poettgen, Rainer; Eckert, Hellmut; Sao Paulo Univ., Sao Carlos

2017-01-01

The ordered Laves phases RE_2Rh_3Ga (RE=Y, La-Nd, Sm, Gd-Er) were synthesized by arc-melting of the elements and subsequent annealing. The samples were characterized by powder X-ray diffraction (XRD). They crystallize with the rhombohedral Mg_2Ni_3Si type structure, space group R3m. Three structures were refined from single crystal X-ray diffractometer data: a=557.1(1), c=1183.1(2), wR2=0.0591, 159 F"2 values, 10 variables for Y_2Rh_3Ga, a=562.5(2), c=1194.4(2) pm, wR2=0.0519, 206 F"2 values, 11 variables for Ce_2Rh_3Ga and a=556.7(2), c=1184.1(3) pm, wR2=0.0396, 176 F"2 values, 11 variables for Tb_2Rh_3Ga. The Rh_3Ga tetrahedra are condensed via common corners and the large cavities left by the network are filled by the rare earth atoms. The RE_2Rh_3Ga Laves phases crystallize with a translationengleiche subgroup of the cubic RERh_2 Laves phases with MgCu_2 type. Magnetic susceptibility measurements reveal Pauli paramagnetism for Y_2Rh_3Ga and La_2Rh_3Ga. Ce_2Rh_3Ga shows intermediate cerium valence while all other RE_2Rh_3Ga phases are Curie-Weiss paramagnets which order magnetically at low temperatures. The "8"9Y and "7"1Ga solid state nuclear magnetic resonance (NMR) spectra of the diamagnetic representative Y_2Rh_3Ga show well-defined single resonances in agreement with an ordered bulk phase. In comparison to the binary Laves phase YRh_2 a strongly increased "8"9Y resonance frequency is observed owing to a higher s-electron spin density at the "8"9Y nuclei as proven by density of states (DOS) calculations.

Stability of Laves Phases in the Cr Zr System

Czech Academy of Sciences Publication Activity Database

Pavlů, Jana; Vřešťál, Jan; Šob, Mojmír

2009-01-01

Roč. 33, č. 2 (2009), s. 382-387 ISSN 0364-5916 R&D Projects: GA ČR GA106/07/1078 Institutional research plan: CEZ:AV0Z20410507 Keywords : ab initio calculations * Laves phases * phase diagrams Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.904, year: 2009

Structural electronic and mechanical properties of YM2 (M=Mn, Fe, Co) laves phase compounds: First principle calculations analyzed with datamining approach

Science.gov (United States)

Saidi, F.; Sebaa, N.; Mahmoudi, A.; Aourag, H.; Merad, G.; Dergal, M.

2018-06-01

We performed first-principle calculations to investigate structural, phase stability, electronic and mechanical properties for the Laves phases YM2 (M = Mn, Fe, Co) with C15, C14 and C36 structures. We used the density functional theory within the framework of both pseudo-potentials and plane wave basis using VASP (Vienna Ab Initio Software Package). The calculated equilibrium structural parameters are in accordance with available theoretical values. Mechanical properties were calculated, discussed, and analyzed with data mining approach in terms of structure stability. The results reveal that YCo2 is harder than YFe2 and YMn2.

Data on a Laves phase intermetallic matrix composite in situ toughened by ductile precipitates.

Science.gov (United States)

Knowles, Alexander J; Bhowmik, Ayan; Purkayastha, Surajit; Jones, Nicholas G; Giuliani, Finn; Clegg, William J; Dye, David; Stone, Howard J

2017-10-01

The data presented in this article are related to the research article entitled "Laves phase intermetallic matrix composite in situ toughened by ductile precipitates" (Knowles et al.) [1]. The composite comprised a Fe 2 (Mo, Ti) matrix with bcc (Mo, Ti) precipitated laths produced in situ by an aging heat treatment, which was shown to confer a toughening effect (Knowles et al.) [1]. Here, details are given on a focused ion beam (FIB) slice and view experiment performed on the composite so as to determine that the 3D morphology of the bcc (Mo, Ti) precipitates were laths rather than needles. Scanning transmission electron microscopy (S(TEM)) micrographs of the microstructure as well as energy dispersive X-ray spectroscopy (EDX) maps are presented that identify the elemental partitioning between the C14 Laves matrix and the bcc laths, with Mo rejected from the matrix into laths. A TEM selected area diffraction pattern (SADP) and key is provided that was used to validate the orientation relation between the matrix and laths identified in (Knowles et al.) [1] along with details of the transformation matrix determined.

Data on a Laves phase intermetallic matrix composite in situ toughened by ductile precipitates

Directory of Open Access Journals (Sweden)

Alexander J. Knowles

2017-10-01

Full Text Available The data presented in this article are related to the research article entitled “Laves phase intermetallic matrix composite in situ toughened by ductile precipitates” (Knowles et al. [1]. The composite comprised a Fe2(Mo, Ti matrix with bcc (Mo, Ti precipitated laths produced in situ by an aging heat treatment, which was shown to confer a toughening effect (Knowles et al. [1]. Here, details are given on a focused ion beam (FIB slice and view experiment performed on the composite so as to determine that the 3D morphology of the bcc (Mo, Ti precipitates were laths rather than needles. Scanning transmission electron microscopy (S(TEM micrographs of the microstructure as well as energy dispersive X-ray spectroscopy (EDX maps are presented that identify the elemental partitioning between the C14 Laves matrix and the bcc laths, with Mo rejected from the matrix into laths. A TEM selected area diffraction pattern (SADP and key is provided that was used to validate the orientation relation between the matrix and laths identified in (Knowles et al. [1] along with details of the transformation matrix determined.

Alumina-Forming Austenitic Stainless Steels Strengthened by Laves Phase and MC Carbide Precipitates

Science.gov (United States)

Yamamoto, Y.; Brady, M. P.; Lu, Z. P.; Liu, C. T.; Takeyama, M.; Maziasz, P. J.; Pint, B. A.

2007-11-01

Creep strengthening of Al-modified austenitic stainless steels by MC carbides or Fe2Nb Laves phase was explored. Fe-20Cr-15Ni-(0-8)Al and Fe-15Cr-20Ni-5Al base alloys (at. pct) with small additions of Nb, Mo, W, Ti, V, C, and B were cast, thermally-processed, and aged. On exposure from 650 °C to 800 °C in air and in air with 10 pct water vapor, the alloys exhibited continuous protective Al2O3 scale formation at an Al level of only 5 at. pct (2.4 wt pct). Matrices of the Fe-20Cr-15Ni-5Al base alloys consisted of γ (fcc) + α (bcc) dual phase due to the strong α-Fe stabilizing effect of the Al addition and exhibited poor creep resistance. However, adjustment of composition to the Fe-15Cr-20Ni-5Al base resulted in alloys that were single-phase γ-Fe and still capable of alumina scale formation. Alloys that relied solely on Fe2Nb Laves phase precipitates for strengthening exhibited relatively low creep resistance, while alloys that also contained MC carbide precipitates exhibited creep resistance comparable to that of commercially available heat-resistant austenitic stainless steels. Phase equilibria studies indicated that NbC precipitates in combination with Fe2Nb were of limited benefit to creep resistance due to the solution limit of NbC within the γ-Fe matrix of the alloys studied. However, when combined with other MC-type strengtheners, such as V4C3 or TiC, higher levels of creep resistance were obtained.

Computational thermodynamic investigations of growth and coarsening of laves phase precipitates in 12%Cr creep resistant steels

Energy Technology Data Exchange (ETDEWEB)

Prat, O.; Rojas, D. [Max-Planck-Institut fuer Eisenforschung GmbH, Duesseldorf (Germany); Garcia, J.; Kaysser-Pyzalla, A.R. [Helmholtz-Zentrum Berlin fuer Materialien und Energie GmbH, Berlin (Germany); Bochum Univ. (Germany)

2010-07-01

Precipitation phenomena in 12%Cr high alloyed steels have been investigated at creep conditions of 650 and 150 MPa up to 6.500 hours in two different alloys. Growth and coarsening of Laves phase was determined experimentally by measuring the size of Laves phase on crept samples using scanning transmission electron microscopy (STEM). The simulations were performed using the software DICTRA based on the assumption the local equilibrium at the moving phase interface. For equilibrium calculations, the Thermo-Calc software was used. The experimental results were compared with DICTRA simulations, showing good agreement. Both the quantitative metallographic measurements as well as the simulations indicate very low coarsening for Laves Phase. The influence of different elements such as Co, Si and Cu on coarsening for Laves phase was simulated. (orig.)

Room and high temperature deformation behaviour of a forged Fe–15Al–5Nb alloy with a reinforcing dispersion of equiaxed Laves phase particles

International Nuclear Information System (INIS)

Morris, D.G.; Muñoz-Morris, M.A.

2012-01-01

Highlights: ► Forged Fe–15%Al–5%Nb has a composite structure of soft matrix with equiaxed Laves phase particles. ► The material shows good strength with excellent ductility at room temperature. ► Good creep strength is maintained to 700 °C. ► The coarse composite microstructure ensures good long term stability at high temperatures. ► High temperature strength depends on load sharing between phases and microstructural refinement. - Abstract: The cast-in network of continuous Laves phase in a Fe–15%Al–5%Nb alloy has been converted to a dispersion of coarse Laves phase particles by high temperature forging, and the room temperature and high temperature deformation behaviour examined. The material shows good room temperature tensile ductility and good creep strength at temperatures up to 700 °C. The good high temperature strength is explained by the refinement of substructure by the dispersion of Laves phase particles and load and strain partitioning between the stiff and hard phase and the softer matrix. The relatively coarse microstructure is expected to be highly stable against coarsening at high temperatures, which should allow retention of creep properties even for long exposure times.

Effect of prior deformation on microstructural development and Laves phase precipitation in high-chromium stainless steel.

Science.gov (United States)

Hsiao, Z-W; Chen, D; Kuo, J-C; Lin, D-Y

2017-04-01

This study investigated the influence of deformation on precipitation behaviour and microstructure change during annealing. Here, the prior deformation of high-chromium stainless steel was tensile deformation of 3%, 6% and 10%, and the specimens were then annealed at 700˚C for 10 h. The specimens were subsequently analyzed using backscattered electron image and electron backscattering diffraction measurements with SEM. Compared with the deformation microstructure, the grains revealed no preferred orientation. The precipitates of TiN and NbC were formed homogenously in the grain interior and at grain boundaries after annealing. Fine Laves phase precipitates were observed in grains and along subgrain boundaries as the deformation increased. Furthermore, the volume fraction of Laves phase increased, but the average particle diameter of precipitate was reduced as the deformation increased. © 2017 The Authors Journal of Microscopy © 2017 Royal Microscopical Society.

High pressure studies of YMn{sub 2} Laves phase and its deuterides

Energy Technology Data Exchange (ETDEWEB)

Sugiura, H.; Paul-Boncour, V.; Percheron-Guegan, A.; Marchuk, I.; Hirata, T.; Filipek, S.M.; Dorogova, M

2004-03-24

The C15 Laves phase intermetallic YMn{sub 2} and its deuterides containing 1.15, 2, 3.4 and 4 deuterium (D) atoms per formula unit (pfu) (the structure of YMn{sub 2}D{sub 4} is rhombohedral whereas other three deuterides preserve the cubic C15 structure) were compressed up to 31 GPa by using diamond anvil cell (DAC). Parameters of equation of state (EOS) were derived for all phases investigated. The discontinuous change of bulk modulus under high pressure has been revealed for all samples investigated. Two deuterides, YMn{sub 2}D{sub 1.15} and YMn{sub 2}D{sub 2}, decomposed reversibly under pressure into two phases: poor and enriched in deuterium.

Growth Kinetics of Laves Phase and Its Effect on Creep Rupture Behavior in 9Cr Heat Resistant Steel

Institute of Scientific and Technical Information of China (English)

Zhi-xin XIA; Chuan-yang WANG; Chen LEI; Yun-ting LAI; Yan-fen ZHAO; Lu ZHANG

2016-01-01

The effects of Laves phase formation and growth on creep rupture behaviors of P92 steel at 883 K were studied.The microstructural evolution was characterized using scanning electron microscopy and transmission elec-tron microscopy.Kinetic modeling was carried out using the software DICTRA.The results indicated Fe2 (W,Mo) Laves phase has formed during creep with 200 MPa applied stress at 883 K for 243 h.The experimental results showed a good agreement with thermodynamic calculations.The plastic deformation of laths is the main reason of creep rupture under the applied stress beyond 160 MPa,whereas,creep voids initiated by coarser Laves phase play an effective role in creep rupture under the applied stress lower than 160 MPa.Laves phase particles with the mean size of 243 nm lead to the change of creep rupture feature.Microstructures at the vicinity of fracture surface,the gage portion and the threaded ends of creep rupture specimens were also observed,indicating that creep tensile stress enhances the coarsening of Laves phase.

Hydrogen diffusion in the Laves-phase compound TiCr1.78

International Nuclear Information System (INIS)

Mazzolai, G.; Coluzzi, B.; Biscarini, A.; Mazzolai, F.M.; Tuissi, A.; Agresti, F.; Principi, G.; Lo Russo, S.

2009-01-01

The temperature dependence of the Young's modulus and of the internal friction (IF) has been investigated between 80 and 300 K at acoustical frequencies in the hexagonal (C14) Laves-phase TiCr 1.78 charged with hydrogen. In this compound H occupies tetrahedral interstitial sites which are grouped in interlinked hexagons. A mechanical relaxation has been found at around 120 K (f = 5.4 kHz), which appears to be due to tunnelling transitions of delocalized H from one hexagon to the other. The rate of H absorption has been investigated at high temperature (660-1200 K) and the H diffusion coefficient has been derived from the pressure measurement as a function of time. A cumulative Arrhenius plot of IF and absorption diffusion data exhibits a non-exponential behaviour, which is due to a change in the diffusion mechanism from over-barrier hopping at high temperature to phonon-assisted tunnelling at low temperature.

Li{sub 12}Cu{sub 12.60}Al{sub 14.37}. A new ternary derivative of the binary Laves phases

Energy Technology Data Exchange (ETDEWEB)

Pavlyuk, Volodymyr [Ivan Franko Lviv National Univ. (Ukraine). Dept. of Inorganic Chemistry; Jan Dlugosz Univ., Czestochowa (Poland). Inst. of Chemistry, Environment Protection and Biotechnology; Dmytriv, Grygoriy; Tarasiuk, Ivan [Ivan Franko Lviv National Univ. (Ukraine). Dept. of Inorganic Chemistry; Chumak, Ihor [IFW Dresden (Germany); Ehrenberg, Helmut [Karlsruhe Institute of Technology (KIT), Karlsruhe (Germany). Inorganic Chemistry

2011-12-15

New ternary dodecalithium dodecacopper tetradecaaluminium, Li{sub 12}Cu{sub 12.60}Al{sub 14.37} (trigonal, R anti 3m, hR39), crystallizes as a new structure type and belongs to the structural family that derives from binary Laves phases. The Li atoms are enclosed in 15- and 16-vertex and the Al3 atom in 14-vertex pseudo-Frank-Kasper polyhedra. The polyhedra around the statistical mixtures of (Cu,Al)1 and (Al,Cu)2 are distorted icosahedra. The electronic structure was calculated by the TB- LMTO-ASA (tight-binding linear muffin-tin orbital atomic spheres approximation) method. The electron localization function, which indicates bond formation, is mostly located at the Al atoms. Thus, Al-Al bonding is much stronger than Li-Al or Cu-Al bonding. This indicates that, besides metallic bonding which is dominant in this compound, weak covalent Al-Al interactions also exist. (orig.)

Ternary rhombohedral Laves phases RE{sub 2}Rh{sub 3}Ga (RE = Y, La-Nd, Sm, Gd-Er)

Energy Technology Data Exchange (ETDEWEB)

Seidel, Stefan; Benndorf, Christopher; Heletta, Lukas; Poettgen, Rainer [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie; Janka, Oliver [Oldenburg Univ. (Germany). Inst. fuer Chemie; Mausolf, Bernhard [RWTH Aachen (Germany). Inst. fuer Anorganische Chemie; Haarmann, Frank [RWTH Aachen (Germany). Inst. fuer Anorganische Chemie; Max-Planck-Institut fuer Chemische Physik fester Stoffe, Dresden (Germany); Eckert, Hellmut [Muenster Univ. (Germany). Inst. fuer Physikalische Chemie; Sao Paulo Univ., Sao Carlos (Brazil). Inst. of Physics

2017-06-01

The ordered Laves phases RE{sub 2}Rh{sub 3}Ga (RE=Y, La-Nd, Sm, Gd-Er) were synthesized by arc-melting of the elements and subsequent annealing. The samples were characterized by powder X-ray diffraction (XRD). They crystallize with the rhombohedral Mg{sub 2}Ni{sub 3}Si type structure, space group R3m. Three structures were refined from single crystal X-ray diffractometer data: a=557.1(1), c=1183.1(2), wR2=0.0591, 159 F{sup 2} values, 10 variables for Y{sub 2}Rh{sub 3}Ga, a=562.5(2), c=1194.4(2) pm, wR2=0.0519, 206 F{sup 2} values, 11 variables for Ce{sub 2}Rh{sub 3}Ga and a=556.7(2), c=1184.1(3) pm, wR2=0.0396, 176 F{sup 2} values, 11 variables for Tb{sub 2}Rh{sub 3}Ga. The Rh{sub 3}Ga tetrahedra are condensed via common corners and the large cavities left by the network are filled by the rare earth atoms. The RE{sub 2}Rh{sub 3}Ga Laves phases crystallize with a translationengleiche subgroup of the cubic RERh{sub 2} Laves phases with MgCu{sub 2} type. Magnetic susceptibility measurements reveal Pauli paramagnetism for Y{sub 2}Rh{sub 3}Ga and La{sub 2}Rh{sub 3}Ga. Ce{sub 2}Rh{sub 3}Ga shows intermediate cerium valence while all other RE{sub 2}Rh{sub 3}Ga phases are Curie-Weiss paramagnets which order magnetically at low temperatures. The {sup 89}Y and {sup 71}Ga solid state nuclear magnetic resonance (NMR) spectra of the diamagnetic representative Y{sub 2}Rh{sub 3}Ga show well-defined single resonances in agreement with an ordered bulk phase. In comparison to the binary Laves phase YRh{sub 2} a strongly increased {sup 89}Y resonance frequency is observed owing to a higher s-electron spin density at the {sup 89}Y nuclei as proven by density of states (DOS) calculations.

Aging behavior and mechanical properties of maraging steels in the presence of submicrocrystalline Laves phase particles

International Nuclear Information System (INIS)

Mahmoudi, A.; Ghavidel, M.R. Zamanzad; Nedjad, S. Hossein; Heidarzadeh, A.; Ahmadabadi, M. Nili

2011-01-01

Cold rolling and annealing of homogenized Fe-Ni-Mn-Mo-Ti-Cr maraging steels resulted in the formation of submicrocrystalline Fe 2 (Mo,Ti) Laves phase particles. Optical and scanning electron microscopy, X-ray diffraction, tensile and hardness tests were used to study the microstructure, aging behavior and mechanical properties of the annealed steels. The annealed microstructures showed age hardenability during subsequent isothermal aging at 753 K. Ultrahigh fracture stress but poor tensile ductility was obtained after substantial age hardening in the specimens with 2% and 4% chromium. Increasing chromium addition up to 6% toughened the aged microstructure at the expense of the fracture stress by increasing the volume fraction of retained austenite. The Laves phase particles acted as crack nucleation sites during tensile deformation. - Highlights: → Laves phases dispersed in a BCC iron matrix by annealing of cold rolled samples. → The samples showed age hardenability during subsequent isothermal aging at 753 K. → Ultrahigh fracture stress but poor ductility was obtained after age hardening. → Increasing chromium addition toughened the aged microstructure. → Laves phase particles acting as crack nucleation sites during tensile deformation.

Structure and Phase Transformation in the Giant Magnetostriction Laves-Phase SmFe₂

Energy Technology Data Exchange (ETDEWEB)

Liu, Xiaonan; Lin, Kun; Gao, Qilong; Zhu, He; Li, Qiang; Cao, Yili; Liu, Zhanning; You, Li; Chen, Jun; Ren, Yang [Argonne National Laboratory, X-Ray Science Division, Argonne, Illinois 60439, United States; Huang, Rongjin [Key Laboratory; Lapidus, Saul H. [Argonne National Laboratory, X-Ray Science Division, Argonne, Illinois 60439, United States; Xing, Xianran

2017-10-13

As one class of the most important intermetallic compounds, the binary Laves-phase is well-known for their abundant magnetic properties. Samarium-iron alloy system, SmFe₂, is a prototypical Laves compound that shows strong negative magnetostriction but relatively weak magnetocrystalline anisotropy. SmFe₂ has been identified as a cubic Fd$ \\overline{3}\\ $m structure at room temperature, however, the cubic symmetry does not match the spontaneous magnetization along the [111]_cubic direction. Here we studied the crystal structure of SmFe₂ by high-resolution synchrotron X-ray powder diffraction and X-ray total scattering methods. SmFe₂ is found to adopt a centrosymmetric trigonal R$ \\overline{3}\\ $m structure at room temperature, which transforms to an orthorhombic Imma structure at 200 K. This transition is in agreement with the changes of easy magnetization direction from [111]_cubic to [110]_cubic direction, and is further evidenced by the inflexion of thermal expansion behavior, the sharp decline of the magnetic susceptibility in the FC-ZFC curve, and the anomaly in the specific heat capacity measurement. The revised structure and phase transformation of SmFe₂ could be useful to understand the magnetostriction and related physical properties of other RM₂-type pseudo-cubic Laves-phase intermetallic compounds.

Hydrogen diffusion in the Laves-phase compound TiCr{sub 1.78}

Energy Technology Data Exchange (ETDEWEB)

Mazzolai, G. [University of Perugia, Department of Physics, Via A. Pascoli 5, 06100 Perugia (Italy); Universita Telematica e-Campus, Via Isimbardi 10, Novedrate (Colombia) (Italy); Coluzzi, B.; Biscarini, A. [University of Perugia, Department of Physics, Via A. Pascoli 5, 06100 Perugia (Italy); Mazzolai, F.M., E-mail: fabio.mazzolai@fisica.unipg.it [University of Perugia, Department of Physics, Via A. Pascoli 5, 06100 Perugia (Italy); Tuissi, A. [Institute for Energy and Interphases, CNR-IENI, C.so Promessi Sposi, 29, Lecco (Italy); Agresti, F.; Principi, G. [University of Padua, Dept. of Mech. Eng., via Marzolo 8, 35131 Padua (Italy); Lo Russo, S. [University of Padua, Physics Dept., via Marzolo 8, 35131 Padua (Italy)

2009-09-15

The temperature dependence of the Young's modulus and of the internal friction (IF) has been investigated between 80 and 300 K at acoustical frequencies in the hexagonal (C14) Laves-phase TiCr{sub 1.78} charged with hydrogen. In this compound H occupies tetrahedral interstitial sites which are grouped in interlinked hexagons. A mechanical relaxation has been found at around 120 K (f = 5.4 kHz), which appears to be due to tunnelling transitions of delocalized H from one hexagon to the other. The rate of H absorption has been investigated at high temperature (660-1200 K) and the H diffusion coefficient has been derived from the pressure measurement as a function of time. A cumulative Arrhenius plot of IF and absorption diffusion data exhibits a non-exponential behaviour, which is due to a change in the diffusion mechanism from over-barrier hopping at high temperature to phonon-assisted tunnelling at low temperature.

Theoretical and Experimental Investigation on the Low Temperature Properties of the NbCr{sub 2} Laves Phase

Energy Technology Data Exchange (ETDEWEB)

Thoma, D.J.; Chu, F.; Chen, K.C.; Kotula, P.G.; Mitchell, T.E.; Wills, J.M.; Ormeci, A.; Chen, S.P.; Albers, R.C.

1999-06-03

This is the final report of a three-year, Laboratory Directed Research and Development (LDRD) project at Los Alamos National Laboratory (LANL). The goal of the project was to develop methodologies in which to define and improve the properties of NbCr{sub 2} so that the high temperature structural applications of alloys based upon this would not be limited by the low-temperature brittle behavior of the intermetallic. We accomplished this task by (1) understanding the defect structure and deformation mechanisms in Laves phases, (2) electronic and geometric contributions to phase stability and alloying behavior, and (3) novel processing of dual phase (Laves/bcc) structures. As a result alloys with properties that in many cases surpass superalloys were developed. For example, we have tailored alloy design strategies and processing routes in a metal alloy to achieve ambient temperature ultimate strengths of 2.35 GPa as well as ultimate strengths of 1.5 GPa at 1000 C. This results i n one of the strongest metal alloys that currently exist, while still having deformability at room temperature.

The Cr–Fe–Nb ternary system: Experimental isothermal sections at 700 °C, 1050 °C and 1350 °C

Energy Technology Data Exchange (ETDEWEB)

Jacob, Aurélie, E-mail: a.jacob@fz-juelich.de [Forschungszentrum Juelich, IEK-2, 52425 Juelich (Germany); Schmetterer, Clemens [Forschungszentrum Juelich, IEK-2, 52425 Juelich (Germany); Fraunhofer-UMSICHT, 92237 Sulzbach-Rosenberg (Germany); Grüner, Daniel; Wessel, Egbert [Forschungszentrum Juelich, IEK-2, 52425 Juelich (Germany); Hallstedt, Bengt [Institute for Materials Applications in Mechanical Engineering, RWTH Aachen University, Augustinerbach 4, 52062 Aachen (Germany); Singheiser, Lorenz [Forschungszentrum Juelich, IEK-2, 52425 Juelich (Germany)

2015-11-05

The Cr–Fe–Nb system is an important constituent system in the development of Laves-phase reinforced steels. It contains two Laves-phase polytypes, i.e. C14–Fe{sub 2}Nb and C15–Cr{sub 2}Nb. While the first forms a substantial ternary solid solution with Cr, the latter only shows a limited solubility for Fe. The phase equilibria in the Cr–Fe–Nb system are shown in three isothermal sections at 700, 1050 and 1350 °C. Scanning electron microscopy coupled with energy dispersive X-ray analysis (SEM/EDX), X-ray diffraction (XRD) and electron back scatter diffraction (EBSD) were used to determine the phase equilibria from which the isothermal sections were constructed. - Highlights: • Determination of Phase Equilibria in the Cr–Fe–Nb system at 700, 1050 and 1350 °C. • Isothermal sections at 700, 1050 and 1350 °C were established. • Homogeneity range of Laves phases were determined. • Solubility of Fe and Cr and lattice parameter evolution in the ternary phases were determined.

Laves phase UTi2 stabilized by hydrogen and its magnetic properties

Science.gov (United States)

Buturlim, V.; Havela, L.; Sowa, S.; Kim-Ngan, N.-. T. H.; Paukov, M.; Drozdenko, D.; Dopita, M.; Minarik, P.; Mašková, S.

2018-05-01

We describe basic magnetic properties of uranium-based hydrides UTi2Hx, reported in literature as a cubic Laves phase, although the UTi2 binary phase does not exist. Using a high-temperature hydrogenation, we successfully synthesized two types of such hydrides, presumably with different H concentrations, one with a smaller lattice parameter a = 850.3 pm, which is a paramagnet close to the verge of magnetic ordering, the other with a = 858.8 pm, with a ferromagnetic ground state and ordering temperature TC = 54 K.

Structural, electronic and elastic properties of REIr{sub 2} (RE=La and Ce) Laves phase compounds

Energy Technology Data Exchange (ETDEWEB)

Shrivastava, Deepika, E-mail: deepika89shrivastava@gmail.com; Fatima, Bushra; Sanyal, Sankar P. [Department of Physics, Barkatullah University, Bhopal, 462026 (India)

2016-05-23

REIr{sub 2} (RE = La and Ce) Laves phase intermetallic compounds were investigated with respect to their structural, electronic and elastic properties using full potential linearized augmented plane wave (FP-LAPW) method within generalized gradient approximation (GGA) as implemented in WIEN2k code. The ground state properties such as lattice constants (a{sub 0}), bulk modulus (B), pressure derivative of bulk modulus (B′) and density of state at Fermi level N(E{sub F}) have been obtained by optimization method. The electronic structure (BS, TDOS and PDOS) reveals that these Laves phase compounds are metallic in nature. The calculated elastic constants indicate that these compounds are mechanically stable at ambient pressure and found to be ductile in nature.

Multifunctional phenomena in rare-earth intermetallic compounds with a laves phase structure: giant magnetostriction and magnetocaloric effect

Czech Academy of Sciences Publication Activity Database

Tereshina, I.; Cwik, J.; Tereshina, Evgeniya; Politova, G.; Burkhanov, G.; Chzhan, V.; Ilyushin, A.; Miller, M.; Zaleski, A.; Nenkov, K.; Schultz, L.

2014-01-01

Roč. 50, č. 11 (2014), s. 2504604 ISSN 0018-9464 Institutional support: RVO:68378271 Keywords : giant magnetostriction * Laves phase structure * magnetic anisotropy * magnetocaloric effect * rare-earth intermetallic Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.386, year: 2014

Structural, electronic and elastic properties of RERu{sub 2} (RE=Pr and Nd) Laves phase intermetallic compounds

Energy Technology Data Exchange (ETDEWEB)

Shrivastava, Deepika, E-mail: deepika89shrivastava@gmail.com; Sanyal, Sankar P. [Department of Physics, Barkatullah university, Bhopal, 462026 (India)

2016-05-06

We have performed the first-principles calculations to study the structural, electronic and elastic properties of RERu{sub 2} (RE = Pr and Nd) Laves phase intermetallic compounds using full-potential linearized augmented plane wave (FP-LAPW) method based on density functional theory (DFT) within the generalized gradient approximation (GGA) for exchange and correlation potential. The optimized lattices constant are in reasonable agreement with available experimental data. The electronic properties are analyzed in terms of band structures, total and partial density of states, which confirm their metallic character. The calculated elastic constants infer that these compounds are mechanically stable in C15 (MgCu{sub 2} type) structure and found to be ductile in nature.

First-principles study of structural phase transition, electronic, elastic and thermodynamic properties of C15-type Laves phase TiCr2 under pressure

Science.gov (United States)

He, Li-Zhi; Zhu, Jun; Zhang, Lin

2018-02-01

Phase transition of TiCr2 in C15 (MgCu2), C36 (MgNi2), C14 (MgZn2) structures have been studied by using the projector augmented wave method. It is found that C15-type is the most stable structure, which agrees with the results of Chen et al. At 0 K, the phase boundary of C15 to C36 is 207.79 GPa, and the phase transition from C36 to C14 is 265.61 GPa. Both the transition pressures decrease with increasing temperature. Phonon dispersion and elastic constants are calculated and found that C15-type TiCr2 is mechanically stable according to the elastic stability criteria and phonon dispersion analysis. Moreover, the pressure and temperature dependence of the specific heat, Debye temperature and thermal expansion coefficient are discussed, among them our calculated Debye temperature is consistent with the report of A. sari et al., however, it is far from the results of B. Mayer et al. and Chen et al.

Study of fatigue and fracture behavior of NbCr{sub 2}-based alloys: Phase stability in Nb-Cr-Ni ternary system

Energy Technology Data Exchange (ETDEWEB)

Zhu, J.H.; Liaw, P.K. [Univ. of Tennessee, Knoxville, TN (United States). Dept. of Materials Science and Engineering; Liu, C.T. [Oak Ridge National Lab., TN (United States). Metals and Ceramics Div.

1997-12-01

Phase stability in a ternary Nb-Cr-Ni Laves phase system was studied in this paper. Their previous study in NbCr{sub 2}-based transition-metal Laves phases has shown that the average electron concentration factor, e/a, is the dominating factor in controlling the phase stability of NbCr{sub 2}-based Laves phases when the atomic size ratios are kept identical. Since Ni has ten out-shell electrons, the substitution of Ni for Cr in NbCr{sub 2} will increase the average electron concentration of the alloy, thus leading to the change of the crystal structures from C15 to C14. In this paper, a number of pseudo-binary Nb(Cr,Ni){sub 2} alloys were prepared, and the crystal structures of the alloys after a long heat-treatment at 1000 C as a function of the Ni content were determined by the X-ray diffraction technique. The boundaries of the C15/C14 transition were determined and compared to their previous predictions. It was found that the electron concentration and phase stability correlation is obeyed in the Nb-Cr-Ni system. However, the e/a ratio corresponding to the C15/C14 phase transition was found to move to a higher value than the predicted one. The changes in the lattice constant, Vickers hardness and fracture toughness were also determined as a function of the Ni content, which were discussed in light of the phase stability difference of the alloys.

Fe-moment instability in Ti{sub 1-x}Sc{sub x}Fe{sub 2} Laves-phase compounds

Energy Technology Data Exchange (ETDEWEB)

Ouladdiaf, B. [Institut Laue-Langevin, BP 156, 38042 GRENOBLE Cedex 09 (France); Deportes, J. [Lab. Louis Neel, CNRS, BP 166, 38042 GRENOBLE Cedex 09 (France); Saoudi, M. [Centre Universitaire de Guelma, GUELMA 24 000 (Algeria)

2002-07-01

The magnetic properties of the pseudo-binary Laves-phase compounds Ti{sub 1-x}Sc{sub x}Fe{sub 2} were investigated by means of magnetisation and high-resolution powder neutron diffraction techniques. For x<0.2 a transition from an antiferromagnetic state to a canted one with a ferromagnetic component in the basal plane is observed, while for 0.2c-axis to a canted one. For x{proportional_to}0.3, an additional first-order transition is observed at low temperature accompanied by a large magnetovolume anomaly due to the increase of the intrinsic moment of the Fe atoms at the 2a site. (orig.)

Structural, electronic and elastic properties of heavy fermion YbRh2 Laves phase compound

Science.gov (United States)

Pawar, Harsha; Shugani, Mani; Aynyas, Mahendra; Sanyal, Sankar P.

2018-05-01

The structural, electronic and elastic properties of YbRh2 Laves phase intermetallic compound which crystallize in cubic (MgCu2-type) structure have been investigated using ab-initio full potential linearized augmented plane wave (FP- LAPW) method with LDA and LDA+U approximation. The calculated ground state properties such as lattice parameter (a0), bulk modulus (B) and its pressure derivative (B') are in good agreement with available experimental and theoretical data. The electronic properties are analyzed from band structures and density of states. Elastic constants are predicted first time for this compound which obeys the stability criteria for cubic system.

Microstructure and mechanical properties of two Z-phase strengthened 12%Cr martensitic steels: the effects of Cu and C

Energy Technology Data Exchange (ETDEWEB)

Rashidi, Masoud, E-mail: masoud.rashidi@chalmers.se [Department of Physics, Chalmers University of Technology, SE-412 96 Gothenburg (Sweden); Johansson, Lennart [Siemens Industrial Turbomachinery AB, SE-612 83 Finspong (Sweden); Andrén, Hans-Olof; Liu, Fang [Department of Physics, Chalmers University of Technology, SE-412 96 Gothenburg (Sweden)

2017-05-10

Z-phase strengthened 12% Cr steels are designed to combine good corrosion and creep resistance for applications in fossil fuel power plants with steam temperatures up to 650 °C. Two trial Z-phase strengthened steels were investigated, Z-steel with ultra-low C content, and ZCuC-steel with relatively high C content and Cu addition. The Z-steel has better creep strength; however, the alloy has low impact toughness due to the formation of continuous Laves-phase films at grain boundaries. Atom probe tomography, transmission electron microscopy, and scanning electron microscopy were employed to study the effects of C and Cu on the microstructure of the two steels in the as-tempered condition, and after ageing for different times. The Z-steel shows a fast transformation from TaN to Z-phase. The relatively high C content in the ZCuC-steel resulted in the formation of two categories of MX: Ta(C, N) and TaN. The phase transformation from Ta(C, N) to Z-phase is slower compared to that from TaN to Z-phase. In addition, precipitation of M{sub 23}C{sub 6} and Cu particles in the ZCuC-steel led to easier nucleation of Laves-phase, and hence a much improved toughness.

Laves intermetallics in stainless steel-zirconium alloys

International Nuclear Information System (INIS)

Abraham, D.P.; McDeavitt, S.M.; Richardson, J.W. Jr.

1997-01-01

Laves intermetallics have a significant effect on properties of metal waste forms being developed at Argonne National Laboratory. These waste forms are stainless steel-zirconium alloys that will contain radioactive metal isotopes isolated from spent nuclear fuel by electrometallurgical treatment. The baseline waste form composition for stainless steel-clad fuels is stainless steel-15 wt.% zirconium (SS-15Zr). This article presents results of neutron diffraction measurements, heat-treatment studies and mechanical testing on SS-15Zr alloys. The Laves intermetallics in these alloys, labeled Zr(Fe,Cr,Ni) 2+x , have both C36 and C15 crystal structures. A fraction of these intermetallics transform into (Fe,Cr,Ni) 23 Zr 6 during high-temperature annealing; the authors have proposed a mechanism for this transformation. The SS-15Zr alloys show virtually no elongation in uniaxial tension, but exhibit good strength and ductility in compression tests. This article also presents neutron diffraction and microstructural data for a stainless steel-42 wt.% zirconium (SS-42Zr) alloy

Electron diffraction analysis of an AB{sub 2}-type Laves phase for hydrogen battery applications

Energy Technology Data Exchange (ETDEWEB)

Shi, Z.; Chumbley, S.; Laabs, F.C. [Iowa State Univ., Ames, IA (United States). Ames Lab.

2000-11-16

A multicomponent AB{sub 2} type nickel-metal hydride (Ni-MH) battery alloy prepared by high-pressure gas atomization (HPGA) was investigated by transmission electron microscopy (TEM) in both the as-atomized and heat treated condition. TEM examination showed a heavily faulted dendritic growth structure in as-atomized powder. Selected area diffraction (SAD) showed that this region consisted of both a cubic C15 structure with lattice constant a=7.03 A and an hexagonal C14 structure with lattice parameter a=4.97 A, c=8.11 A. The orientation relationship (OR) between the C14 and C15 structures was determined to be (111)[1 anti 10]{sub C15}//(0001)[11 anti 20]C{sub 14}. An interdendritic phase possessing the C14 structure was also seen. There was also a very fine grain region consisting of the C14 structure. Upon heat treatment, the faulted structure became more defined and appeared as intercalation layers within the grains. Spherical particles rich in Zr and Ni appeared scattered at the grain boundries instead of the C14 interdendritic phase. The polycrystalline region also changed to a mixture of C14 and C15 structures. The phase stability of the C15 and C14 structures based on a consideration of atomic size factor and the average electron concentration is discussed. (orig.)

Precipitation in AISI 316L(N) during creep tests at 550 and 600 °C up to 10 years

Science.gov (United States)

Padilha, A. F.; Escriba, D. M.; Materna-Morris, E.; Rieth, M.; Klimenkov, M.

2007-05-01

The precipitation behaviour in the gauge lengths and in the heads of initially solution annealed type 316L(N) austenitic stainless steel specimens tested in creep at 550 and 600 °C for periods of up to 85 000 h has been studied using several metallographic techniques. Three phases were detected: M 23C 6, Laves, and sigma phase. The volume fraction of the precipitated sigma phase was significantly higher than that of carbides and the Laves phase. M 23C 6 carbide precipitation occurred very rapidly and was followed by the sigma and Laves phases formation in the delta ferrite islands. Sigma and Laves phases precipitated at grain boundaries after longer times. Two different mechanisms of sigma phase precipitation have been proposed, one for delta ferrite decomposition and another for grain boundary precipitation. Small quantities of the Laves phase were detected in delta ferrite, at grain boundaries and inside the grains.

Microstructure of Z-phase strengthened martensitic steels: Meeting the 650°C challenge

DEFF Research Database (Denmark)

Liu, Fang; Rashidi, Masoud; Hald, John

2017-01-01

content in the steels is the governing factor in this transformation. The impact toughness of some test alloys was rather low. This is attributed to the formation of a continuous W-rich film along prior austenite grain boundaries. Cu and C addition to the test alloys changed Laves phase morphology...

Hyperfine spectroscopic study of Laves phase HfFe2

International Nuclear Information System (INIS)

Belosevic-Cavor, J.; Novakovic, N.; Cekic, B.; Ivanovic, N.; Manasijevic, M.

2004-01-01

Hyperfine fields in HfFe 2 were measured at 181 Ta probe using the time-differential perturbed angular correlation method (TDPAC) in the temperature range 78-1200 K. Analysis of the spectra revealed two interactions with hyperfine fields of 13.82(7) T and 8.0(2) T, at 293 K. First is ascribed to the interaction at the 8a position in the cubic C15 structure. The second can be assigned to a minor amount of hexagonal C14 phase, or to an irregular position of the probe in the C15 lattice. Results of calculations using LAPW-WIEN97 are in a good agreement with experiment

X-Ray diffraction on rare earth-3d Laves phase compound ErCo2 in magnetic field

International Nuclear Information System (INIS)

Yagasaki, Katsuma; Notsu, Shiko; Takaesu, Yoshinao; Nakama, Takao; Sakai, Eijiro; Koyama, Keiichi; Watanabe, Kazuo; Burkov, Alexander T.

2006-01-01

X-Ray powder diffraction method is used to investigate the effect of magnetic ordering and external magnetic field on crystal structure of Laves phase intermetallic compound ErCo 2 . The diffraction patterns were recorded at temperatures from 300K down to 8.5K in magnetic field up to 5T. Distortion of the room-temperature cubic structure was found in magnetically ordered state below 32K. The symmetry at low temperature is rhombohedral in agreement with literature results, or lower symmetry than it. However the symmetry of the unit cell increases to cubic in external magnetic field of 5T

Effect of Al content on structure and mechanical properties of the Al{sub x}CrNbTiVZr (x = 0; 0.25; 0.5; 1) high-entropy alloys

Energy Technology Data Exchange (ETDEWEB)

Yurchenko, N.Yu. [Laboratory of Bulk Nanostructured Materials, Belgorod State University, Belgorod 308015 (Russian Federation); Stepanov, N.D., E-mail: stepanov@bsu.edu.ru [Laboratory of Bulk Nanostructured Materials, Belgorod State University, Belgorod 308015 (Russian Federation); Shaysultanov, D.G. [Laboratory of Bulk Nanostructured Materials, Belgorod State University, Belgorod 308015 (Russian Federation); Tikhonovsky, M.A. [National Science Center “Kharkov Institute of Physics and Technology”, NAS of Ukraine, Kharkov, 61108 (Ukraine); Salishchev, G.A. [Laboratory of Bulk Nanostructured Materials, Belgorod State University, Belgorod 308015 (Russian Federation)

2016-11-15

In present study, structure and mechanical properties of the Al{sub x}CrNbTiVZr (x = 0; 0.25; 0.5; 1) high-entropy alloys after arc melting and annealing at 1200 °C for 24 h are investigated. The CrNbTiVZr alloy is composed of body centered cubic (bcc) and C15 (face centered cubic) Laves phases while the Al{sub x}CrNbTiVZr (x = 0.25; 0.5; 1) alloys consist of bcc and two C14 (hexagonal close packed) Laves phases with different chemical compositions. Thermodynamic modeling predicts existence of two phases – bcc and C15 Laves phase and broadening of single bcc phase field due to Al addition. The density of the alloys decreases with the increase of Al content. The alloys are found to be extremely brittle at room temperature and 600 °C. The alloys have high strength at temperatures of 800–1000 °C. For example, yield strength at 800 °C increases from 440 MPa for the CrNbTiVZr alloy to 1250 MPa for the AlCrNbTiVZr alloy. The experimental phase composition of the Al{sub x}CrNbTiVZr alloys is compared with predicted equilibrium phases and the factors governing the transformation of C15 to C14 Laves phases due to Al addition to the CrNbTiVZr alloy analyzed. Specific properties of the alloys are compared with other high-entropy alloys and commercial Ni-based superalloys. - Highlights: •Al{sub x}CrNbTiVZr (x = 0; 0.25; 0.5; 1) alloys are arc melted and annealed at 1200 °C. •The CrNbTiVZr alloy has bcc and C15 Laves phases. •The Al-containing alloys are composed of bcc and two C14 Laves phases. •The alloys demonstrate high specific strength at temperatures of 800 °C and 1000 °C. •The strength of the alloys increases in proportion with increase of Al content.

Production and characterization of monocrystals of the cubic Laves phases Se-Al2

International Nuclear Information System (INIS)

Beyss, M.; Uelhoff, W.; Fattah, A.

1977-04-01

The monocrystals of the cubic Laves phases Se-Al 2 have been produced for special measurements. Low-temperature anomalies were measured which were influenced by doping with foreign atoms. These anomalies, also called Kondo effect, were detected in some physical quantities like electric resistance, magnetic resistance, susceptibility, magnetization, specific heat, thermal conductivity and thermoelectric force. For diffuse magnetic neutron scattering, monocrystals with the dimensions 10 mm diameter and 70 mm length were produced. The materials used were La Al 2 , (La Ce) Al 2 , Ce Al 2 , Y Al 2 , and (Y Ce) Al 2 . The monocrystals had to have an exactly cylindrical cross-section which was obtained by stripping by means of spark erosion machines. The measurements were carried out at the reactor of the Laue-Langevin Institute at Grenoble. In the experiments the magnetic behavior was measured by neutron scattering on monocrystals in the temperature range from 2.5 K to 300 K, the energy spectra having been registered. (orig.) [de

Creep strength and microstructural evolution of 9-12% Cr heat resistant steels during creep exposure at 600 C and 650 C

Energy Technology Data Exchange (ETDEWEB)

Mendez Martin, Francisca [Graz Univ. of Technology (Austria). Inst. for Materials Science and Welding; Panait, Clara Gabriela [MINES ParisTech, UMR CNRS, Evry (France). Centre des Materiaux; V et M France CEV, Aulnoye-Aymeries (France); Bendick, Walter [Salzgitter Mannesmann Forschung GmbH (SZMF), Duisburg (DE)] (and others)

2010-07-01

9-12% Cr heat resistant steels are used for applications at high temperatures and pressures in steam power plants. 12% Cr steels show higher creep strength and higher corrosion resistance compared to 9% Cr steels for short term creep exposure. However, the higher creep strength of 12 %Cr steels drops increasingly after 10,000-20,000 h of creep. This is probably due to a microstructural instability such as the precipitation of new phases (e.g. Laves phases and Z-phases), the growth of the precipitates and the recovery of the matrix. 9% Cr and 12% Cr tempered martensitic steels that have been creep tested for times up to 50,000 h at 600 C and 650 C were investigated using Transmission Electron Microscopy (TEM) on extractive replicas and thin foils together with Backscatter Scanning Electron Microscopy (BSE-SEM) to better understand the different creep behaviour of the two different steels. A significant precipitation of Laves phase and low amounts of Z-phase was observed in the 9% Cr steels after long-term creep exposure. The size distribution of Laves phases was measured by image analysis of SEM-BSE images. In the 12% Cr steel two new phases were identified, Laves phase and Z-phase after almost 30,000 h of creep test. The quantification of the different precipitated phases was studied. (orig.)

Collapse of the magnetic moment under pressure of AFe{sub 2} (A=Y, Zr, Lu and Hf) in the cubic Laves phase

Energy Technology Data Exchange (ETDEWEB)

Zhang, Wenxu, E-mail: xwzhang@uestc.edu.cn; Zhang, Wanli

2016-04-15

The electronic structures of four Laves phase iron compounds (e.g. YFe{sub 2}, ZrFe{sub 2}, LuFe{sub 2} and HfFe{sub 2}) have been calculated with a state-of-the-art full potential electronic structure code. Our theoretical work predicted that the magnetic moments collapse under hydrostatic pressure. This feature is found to be universal in these materials. Its electronic origin is provided by the sharp peaks in the density of states near the Fermi level. It is shown that a first order quantum phase transition can be expected under pressure in Y(Zr, or Lu)Fe{sub 2}, while a second order one in HfFe{sub 2}. The bonding characteristics are discussed to elucidate the equilibrium lattice constant variation. The large spontaneous volume magnetostriction gives one of the most important characteristics of these compounds. Invar anomalies in these compounds can be partly explained by the current work when the fast continuous magnetic moment decrease with the decrease of the lattice constant was properly considered. This work may be as a first insight into the rich world of quantum phase transition and Invar mechanism in these Laves phase compounds. - Highlights: • Magnetic moment of YFe{sub 2}, ZrFe{sub 2}, LuFe{sub 2} and HfFe{sub 2} collapses under pressure. • The transition in Y(Zr or Lu) Fe{sub 2} under pressure is first order. • The transition in HfFe{sub 2} under pressure is second order. • The Invar effects in the compounds can be put into the magnetostriction model.

Structural, Electronic and Elastic Properties of Heavy Fermion YbTM2 (TM= Ir and Pt) Laves Phase Compounds

Science.gov (United States)

Pawar, H.; Shugani, M.; Aynyas, M.; Sanyal, S. P.

2018-02-01

The structural, electronic and elastic properties of YbTM2 (TM = Ir and Pt) Laves phase intermetallic compounds which crystallize in cubic (MgCu2-type) structure, have been investigated using ab-initio full potential linearized augmented plane wave (FP-LAPW) method with LDA and LDA+U approximation. The calculated ground state properties such as lattice parameter (a0), bulk modulus (B) and its pressure derivative (B‧) are in good agreement with available experimental and theoretical data. The electronic properties are analyzed from band structures and density of states. Elastic constants are predicted first time for these compounds which obey the stability criteria for cubic system.

New Phase in the System Uranium-Molybdenum-Silicon; Nouvelle phase dans le systeme uranium-molybdene-silicium; Novaya faza v sisteme uran-molibden'-kremnij; Una fase nueva en el sistema uranio-molibdeno-silicio

Energy Technology Data Exchange (ETDEWEB)

Sikirica, M.; Ban, Z. [Rudjer Bokovic Institute, Zagreb, Yugoslavia (Croatia)

1963-11-15

During the investigation of the ternary system uranium-molybdenum-silicon, a new phase with the composition U{sub 4}Mo{sub 5}-Si{sub 3} was formed. Structure determination exclusively based on the powder data showed that the particular phase belongs to the hexagonal system. Space group P6/mmc or one of the sub-groups is indicated. Unit cell dimensions were found to be a = 5.37{sub 0}A, c = 8 . 58{sub 2}A. A comparison of calculated and observed intensities shows close resemblance to the structure of the Laves phases of the C14-type. (author) [French] Au cours de recherches sur le systeme ternaire uranium-molybdene-silicium, on a constate la formation d'une nouvelle phase, de composition U{sub 4}Mo{sub 5}Si{sub 3}. Une determination de la structure, exclusivement fondee sur des donnees relatives a la poudre, a revele que cette phase particuliere appartenait au systeme hexagonal. Les auteurs indiquent un groupe spatial P6/mmc ou un des sous-groupes. Les dimensions d'une maille individuelle sont donnees par a = 5,37{sub 0}A, c = 8,58{sub 2}A. La comparaison entre l'intensite calculee et Tintensite observee montre une ressemblance etroite avec la structure des phases de Laves du type C-14. (author) [Spanish] En-el curso del estudio del sistema temario uranio-molibdeno-silicio, los autores observaron la formacion de una fase cuya composicion responde a la formula U{sub 4}Mo{sub 5}Si{sub 3}. La determinacion de la estructura, basada exclusivamente en los datos referentes al material en polvo, demuestra que esa fase pertenece al sistema hexagonal. Se senalo la existencia de un grupo especial P6/mmc y se comprobo que las dimensiones de la celda elemental son a = 5,37{sub 0}A, c = 8,58{sub 2}A. La comparacion de las intensidades calculadas con las observadas indica que existe una analogia estrecha con la estructura de la fase de Laves del tipo C 14. (author) [Russian] Pri izuchenii trojnoj sistemy uran - molibden - kremnij obrazovalas' novaya faza sostava U{sub 4}Mo{sub 5

Phase Composition of a CrMo0.5NbTa0.5TiZr High Entropy Alloy: Comparison of Experimental and Simulated Data

Directory of Open Access Journals (Sweden)

Fan Zhang

2013-09-01

Full Text Available Microstructure and phase composition of a CrMo0.5NbTa0.5TiZr high entropy alloy were studied in the as-solidified and heat treated conditions. In the as-solidified condition, the alloy consisted of two disordered BCC phases and an ordered cubic Laves phase. The BCC1 phase solidified in the form of dendrites enriched with Mo, Ta and Nb, and its volume fraction was 42%. The BCC2 and Laves phases solidified by the eutectic-type reaction, and their volume fractions were 27% and 31%, respectively. The BCC2 phase was enriched with Ti and Zr and the Laves phase was heavily enriched with Cr. After hot isostatic pressing at 1450 °C for 3 h, the BCC1 dendrites coagulated into round-shaped particles and their volume fraction increased to 67%. The volume fractions of the BCC2 and Laves phases decreased to 16% and 17%, respectively. After subsequent annealing at 1000 °C for 100 h, submicron-sized Laves particles precipitated inside the BCC1 phase, and the alloy consisted of 52% BCC1, 16% BCC2 and 32% Laves phases. Solidification and phase equilibrium simulations were conducted for the CrMo0.5NbTa0.5TiZr alloy using a thermodynamic database developed by CompuTherm LLC. Some discrepancies were found between the calculated and experimental results and the reasons for these discrepancies were discussed.

Phase behavior and nanoscale structure of phospholipid membranes incorporated with acylated C-14-peptides

DEFF Research Database (Denmark)

Pedersen, T.B.; Kaasgaard, Thomas; Jensen, M.O.

2005-01-01

The thermotropic phase behavior and lateral structure of dipalmitoylphosphatidylcholine (DPPC) lipid bilayers containing an acylated peptide has been characterized by differential scanning calorimetry (DSC) on vesicles and atomic force microscopy (AFM) on mica-supported bilayers. The acylated...... peptide, which is a synthetic decapeptide N-terminally linked to a C-14 acyl chain (C-14-peptide), is incorporated into DPPC bilayers in amounts ranging from 0-20 mol %. The calorimetric scans of the two-component system demonstrate a distinct influence of the C-14-peptide on the lipid bilayer...... gel phase DPPC bilayers, inserts preferentially into preexisting defect regions and has a noticeable influence on the organization of the surrounding lipids. The presence of the C-14-peptide gives rise to a laterally heterogeneous bilayer structure with coexisting lipid domains characterized by a 10...

Constitution of the ternary system Cr–Ni–Ti

International Nuclear Information System (INIS)

Krendelsberger, Natalja; Weitzer, Franz; Du, Yong; Schuster, Julius C.

2013-01-01

Highlights: •Reaction scheme and liquidus surface for Cr-Ni-Ti are given. •In the ternary the C14-type Laves phase coexists with the liquid phase. •Two ternary eutectics are identified. -- Abstract: The nature of solid–liquid phase equilibria in the ternary system Cr–Ni–Ti was investigated using electron microscopy, energy dispersive spectroscopy, X-ray diffraction, and differential thermal analysis. Literature data on solid state phase equilibria are confirmed. The Cr 2 Ti Laves phase modifications coexisting with Ni–Ti phases are clarified to be hexagonal C14-type and cubic C15-type. The C14-type Laves phase γCr 2 Ti is found to coexist with the liquid phase. It forms in the pseudobinary peritectic reaction p max1 from L + β(Cr,Ti) at 1389 °C. On further cooling γCr 2 Ti + NiTi solidify at 1202 °C in the pseudobinary eutectic e max2 . In the Cr-rich part of the system ternary eutectics occur at 1216 °C (E 1 : L = Ni 3 Ti + (Ni) + β(Cr,Ti)) and 1100 °C (E 2 : L = NiTi + Ni 3 Ti + β(Cr,Ti)), respectively. No ternary eutectic is found in the Ti-rich part. Rather the eutectic trough ends in the binary eutectic L = NiTi 2 + β(Ti)

Magnetic frustration and instability in Dy{sub 1-x}La{sub x}Mn{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Ouladdiaf, B. [Institut Laue-Langevin, BP 156, 38042, Grenoble Cedex 9 (France); Ballou, R. [Laboratoire de Magnetisme Louis Neel , CNRS, BP 166, 38042, Grenoble Cedex 9 (France); Deportes, J. [Laboratoire de Magnetisme Louis Neel , CNRS, BP 166, 38042, Grenoble Cedex 9 (France); Lelievre-Berna, E. [Laboratoire de Magnetisme Louis Neel , CNRS, BP 166, 38042, Grenoble Cedex 9 (France)

1995-02-09

A structural dimorphism exists in the Dy{sub 1-x}La{sub x}Mn{sub 2} (0.05{<=}x{<=}0.25) compounds. When the C15 Laves phase is stabilized, no evidence for a long range order is found although the magnetovolume effect is observed at 34 K. When the C14 Laves phase is stabilized, an antiferromagnetic order sets in below 38 K without any magnetovolume effect. ((orig.)).

Phase changes in superaustenitic steels after long-term annealing

Energy Technology Data Exchange (ETDEWEB)

Svoboda, M.; Kroupa, A. [Inst. of Physics of Materials, Academy of Sciences of Czech Republic, Brno (Czech Republic); Sopousek, J.; Vrest' al, J. [Inst. of Theoretical and Physical Chemistry, Masaryk Univ., Brno (Czech Republic); Miodownik, P. [Thermotech Ltd, The Surrey Research Park, Guildford (United Kingdom)

2004-11-01

A structural study was performed on the austenitic steels Avesta 254 SMO and Avesta 654 SMO after annealing at 700 C for 500, 3188, and 6170 h. Both Avesta steels initially show an unexpectedly large amount of the Laves phase, followed by a relatively slow development of the Sigma phase with equilibrium apparently not yet reached after 3188 h. Thermodynamic calculations confirm that the driving forces for alternative precipitates are very similar thus making it easy to form metastable precipitates that only change very slowly to the equilibrium state. TTT calculations also confirm that the Laves phase precipitates earlier than the Sigma phase as the temperature is lowered. (orig.)

The effect of microstructure and temperature on the oxidation behavior of two-phase Cr-Cr2X (X=Nb,Ta) alloys

International Nuclear Information System (INIS)

Brady, M.P.; Tortorelli, P.F.

1998-01-01

The oxidation behavior of Cr(X) solid solution (Cr ss ) and Cr 2 X Laves phases (X = Nb, Ta) was studied individually and in combination at 950--1,100 C in air. The Cr ss phase was significantly more oxidation resistant than the Cr 2 X Laves phase. At 950 C, two-phase alloys of Cr-Cr 2 Nb and Cr-Cr 2 Ta exhibited in-situ internal oxidation, in which remnants of the Cr 2 X Laves phase were incorporated into a growing chromia scale. At 1,100 C, the Cr-Cr 2 Nb alloys continued to exhibit in-situ internal oxidation, which resulted in extensive O/N penetration into the alloy ahead of the alloy-scale interface and catastrophic failure during cyclic oxidation. IN contrast, the Cr-Cr 2 Ta alloys exhibited a transition to selective Cr oxidation and the formation of a continuous chromia scale. The oxidation mechanism is interpreted in terms of multiphase oxidation theory

Influence of hydrogen absorption on magnetic ordering in some zirconium-based Laves phase compounds

International Nuclear Information System (INIS)

Fujii, H.; Pourarian, F.; Wallace, W.E.

1982-01-01

Magnetization measurements were carried out on several zirconium-based hexagonal Laves phase compounds, i.e. the ZrMnsub(2+delta), (Zr,Ti)Mn 2 , Zr(Mn,Fe) 2 and Zr(Fe,Al) 2 systems and their hydrides. The absorbed hydrogen leads to a large increase (20%-30%) in volume without a change in the crystal structure. ZrMnsub(2+delta) is a weak Pauli paramagnet but becomes a spin glass near-ferromagnet by hydriding, indicating that the manganese moments are subjected to competing ferromagnetic and antiferromagnetic coupling tendencies. In the (Zrsub(1-x)Tisub(x))Mn 2 hydrides, ferromagnetic, spin-glass-like, ferromagnetic and antiferromagnetic behaviors appear at 4.2 K in the sequence of increasing x and/or decrease in hydrogen concentration. In the Zr(Mn,Fe) 2 system, the hydrogen absorption increases both the magnetic moments and the magnetic transition temperatures, while absorbed hydrogen leads to suppression of ferromagnetism in the Zr(Fe,Al) 2 system. These varied and complex magnetic behaviors are attributed to the effects of (1) variations in the interatomic distances, (2) changes in the 3d electron concentration and (3) varying local hydrogen concentrations occurring as a result of statistical fluctuations. (Auth.)

Some new experimental results on the Zr-Nb-Fe system

Energy Technology Data Exchange (ETDEWEB)

Ramos, C. [Departamento de Fisica - CAC - Comision Nacional de Energia Atomica, Av. Gral Paz 1499, (1650) San Martin, Buenos Aires (Argentina)]. E-mail: ciramos@cnea.gov.ar; Saragovi, C. [Departamento de Fisica - CAC - Comision Nacional de Energia Atomica, Av. Gral Paz 1499, (1650) San Martin, Buenos Aires (Argentina); Granovsky, M.S. [Departamento de Materiales - CAC - Comision Nacional de Energia Atomica, Av. Gral Paz 1499, (1650) San Martin, Buenos Aires (Argentina)

2007-06-30

The scope of this study is the identification and characterization of intermetallic phases and their binary and ternary fields in the Zr-Nb-Fe phase diagram. A construction of the central region of the phase diagram at 900 {sup o}C was proposed using new experimental results obtained by optical and scanning electron microscopies, X-ray diffraction and microprobe analysis. In addition to the well-known Laves C15-type (ZrNb)Fe{sub 2} phase (the polytypic C14 and C36 structures were not detected in the studied compositions), another Laves C14-type phase was found (Zr(NbFe){sub 2}). Watson and Bennett maps helped to predict the occurrence of both of these phases. Moreover, the validity of the Pettifor prediction model for Laves phases in pseudobinary systems with transition elements was checked, verifying the obtained experimental results in the Zr-Nb-Fe system. On the other hand it was determined that the Zr-Nb-Fe ternary system at 900 {sup o}C, as it happens in the binary Zr-Nb system, would have a miscibility gap ({beta}-Zr + {beta}-Nb) in the 25-70 at.% Nb composition range, accepting up to 3 at.% Fe approximately.

Magnetic, transport and magnetocaloric properties in the Laves phase intermetallic Ho (Co1−xAlx)2 compounds

International Nuclear Information System (INIS)

Ivanova, T.I.; Nikitin, S.A.; Tskhadadze, G.A.; Koshkid’ko, Yu.S.; Suski, W.; Iwasieczko, W.; Badurski, D.

2014-01-01

Highlights: • The Al influence on magnetic properties of the Ho (Co 1-x Al x ) 2 compounds is analyzed. • The first-order magnetic transition appears in sample with Al concentrations x ≤ 0.06. • The MCE and Curie temperature TC demonstrate complex Al concentration dependences. • The magnetoresistance for sample with Al concentration x = 0.06 (58%) is maximum. • High magnetic fields changes the Curie temperature T c of the Ho (Co 1−x Al x ) 2 compounds. - Abstract: The magnetization, magnetoresistivity and magnetocaloric effect (MCE) of the Ho (Co 1−x Al x ) 2 Laves phase intermetallic compounds for x ⩽ 0.2 have been investigated. Complex measurements have been carried out in order to determine the influence of substitution in the Co sublattice by Al on the Co moment, type of the magnetic transition and related properties of these compounds. A comparative analysis of the magnetic, transport and magnetocaloric properties of Ho (Co 1−x Al x ) 2 alloys under various Al concentration is represented. Substitutions at the Co site by Al are found to result in the appearance of itinerant electron metamagnetism (IEM) at the small Al concentrations and in positive magnetovolume effect, leading to an initial increase in the ordering temperature; on the other hand the magnetic phase transition temperature as well as ΔT (MCE) do not depend in direct way on the Al concentration. The 16% increase of magnetocaloric effect for the alloy with x = 0.02 is detected in relation to maternal HoCo 2 . A giant value of magnetoresistivity (58%) is observed for the alloy with the same Al concentration

Modelling of Phase Equlibria in the Hf-V System\

Czech Academy of Sciences Publication Activity Database

Vřešťál, Jan; Pavlů, Jana; Wdowik, U. D.; Šob, Mojmír

2017-01-01

Roč. 53, č. 3 (2017), s. 239-247 ISSN 1450-5339 R&D Projects: GA ČR GA14-15576S; GA MŠk(CZ) LQ1601 Institutional support: RVO:68081723 Keywords : Laves phases * Hf-V system * Ab initio calculations * Phase diagram * Zero Kelvin * CALPHAD method Subject RIV: BM - Solid Matter Physics ; Magnetism OBOR OECD: Condensed matter physics (including formerly solid state physics, supercond.) Impact factor: 0.804, year: 2016

The Effect of Nb Addition on the Microstructure and the High-Temperature Strength of Fe3Al Aluminide

Science.gov (United States)

Kratochvíl, Petr; Švec, Martin; Král, Robert; Veselý, Jozef; Lukáč, Pavel; Vlasák, Tomáš

2018-02-01

The microstructural and high-temperature mechanical properties of Fe-26Al-xNb (x = 3 and 5 at. pct) are compared. The alloys were investigated "as cast" and after hot rolling at 1473 K (1200 °C). Scanning electron microscopes equipped with EDS and EBSD were used for the microstructure and phase identification. The addition of 3 at. pct of Nb into the Fe3Al matrix leads to the formation of C14 λ—Laves phase (Fe,Al)2Nb (LP) particles spread in the Fe3Al matrix, while an eutectic with thin lamellae of LP C14 λ—Laves phase (Fe,Al)2Nb and matrix is also formed in the iron aluminide with 5 at. pct of Nb. The presence of incoherent precipitates is connected with the enhancement of the high-temperature strength and creep resistance.

Thermoelectric properties of TbFe{sub 2} and TbCo{sub 2} in C15- laves phase: Spin-polarized DFT+U approach

Energy Technology Data Exchange (ETDEWEB)

Reshak, A.H., E-mail: maalidph@yahoo.co.uk [New Technologies - Research Centre, University of West Bohemia, Univerzitni 8, Pilsen 306 14 (Czech Republic); School of Material Engineering, University Malaysia Perlis, Kangar, Perlis 01007 (Malaysia)

2017-01-15

Thermoelectric properties of materials are intimately related to their electronic band structure. Combining first- and second-principles calculations, we have obtained the transport properties for the spin-up and spin-down electrons of the laves phase TbFe{sub 2} and TbCo{sub 2} compounds. The unique band structure feature and the density of states at Fermi level (E{sub F}) promote the E{sub F} to a point where carriers are in energetic proximity to these features. The non-zero density of states at E{sub F} for the spin-up (↑) and spin-down (↓) electrons leads to unusual transport properties because both the (↑) and (↓) densities contributes to the states at E{sub F}. The parabolic bands in the vicinity of E{sub F} enhance the carriers mobility and hence the transport properties of TbFe{sub 2} and TbCo{sub 2}. Calculations show that the spin-up/down transport coefficients are temperature-dependent. It has been found that TbCo{sub 2} possess larger Seebeck coefficient than that of TbFe{sub 2} and hence the power factor. The calculated Seebeck coefficient of TbCo{sub 2} agree well with the available experimental data. - Highlights: • The transport properties of TbFe{sub 2} and TbCo{sub 2} are obtained. • The non-zero density of states at E{sub F} leads to unusual transport properties. • Spin-up/down transport coefficients are temperature-dependent. • The calculated Seebeck coefficient of TbCo{sub 2} agree with the experimental data. • TbCo{sub 2} possesses larger Seebeck coefficient than that of TbFe{sub 2}.

Electronic configurations and energies in some thermodynamically correlated laves compounds

International Nuclear Information System (INIS)

Campbell, G.M.

1979-04-01

The known electronic configurations of simple elements in Laves compounds are correlated with those of the more complex systems to determine their electronic configurations and gaseous state promotion energies

Large-scale molecular dynamics simulations of shock waves in Laves crystals and icosahedral quasicrystals

International Nuclear Information System (INIS)

Roth, Johannes

2002-01-01

Quasicrystals and ordinary crystals both possess long-range translational order. But quasicrystals are aperiodic since their symmetry is non-crystallographic. The aim of this project is to study the behavior of shock waves in periodic and aperiodic structures and to compare the results. The expectation is that new types of defects are generated in the aperiodic materials. The materials studied are two models of (AlCu)Li quasicrystals and the C15 Laves phase, a low-order approximant of the quasicrystals. An elastic wave is found in the simulations up to a piston velocity of about up < 0.25 cl. Between 0.5 < up/cl < 0.5 the slope of elastic wave velocity slows down, and a new plastic wave is observed. Extended defect are generated, but no simple two-dimensional walls. The defect bands have finite width and a disordered structure. If the crystal is quenched a polycrystalline phase is obtained. For the quasicrystal the transformation is more complex since ring processes occur in the elastic regime already. Starting at about up < 0.5 cl a single plastic shock wave is observed. In this range all structures are destroyed completely

Predictions of thermomagnetic properties of Laves phase compounds: TbAl2, GdAl2 and SmAl2 performed with ATOMIC MATTERS MFA computation system

Science.gov (United States)

Michalski, Rafał; Zygadło, Jakub

2018-04-01

Recent calculations of properties of TbAl2 GdAl2 and SmAl2 single crystals, performed with our new computation system called ATOMIC MATTERS MFA are presented. We applied localized electron approach to describe the thermal evolution of Fine Electronic Structure of Tb3+, Gd3+ and Sm3+ ions over a wide temperature range and estimate Magnetocaloric Effect (MCE). Thermomagnetic properties of TbAl2, GdAl2 and SmAl2 were calculated based on the fine electronic structure of the 4f8, 4f7 and 4f5 electronic configuration of the Tb3+ and Gd3+ and Sm3+ ions, respectively. Our calculations yielded: magnetic moment value and direction; single-crystalline magnetization curves in zero field and in external magnetic field applied in various directions m(T,Bext); the 4f-electronic components of specific heat c4f(T,Bext); and temperature dependence of the magnetic entropy and isothermal entropy change with external magnetic field - ΔS(T,Bext). The cubic universal CEF parameters values used for all CEF calculations was taken from literature and recalculated for universal cubic parameters set for the RAl2 series: A4 = +7.164 Ka04 and A6 = -1.038 Ka06. Magnetic properties were found to be anisotropic due to cubic Laves phase C15 crystal structure symmetry. These studies reveal the importance of multipolar charge interactions when describing thermomagnetic properties of real 4f electronic systems and the effectiveness of an applied self-consistent molecular field in calculations for magnetic phase transition simulation.

Det særlige ved at lave et projekt i Nationalt Videncenter for Læsning

DEFF Research Database (Denmark)

Lund, Henriette Romme

2009-01-01

Nationalt Videncenter for Læsnings kommunikationskonsulent har interviewet projektdeltagere om, hvor de så det særlige i at lave et projekt i regi af Nationalt Videncenter for Læsning......Nationalt Videncenter for Læsnings kommunikationskonsulent har interviewet projektdeltagere om, hvor de så det særlige i at lave et projekt i regi af Nationalt Videncenter for Læsning...

The effect of hydrogen absorption on the structural, electronic and magnetic properties of the C15 Friauf-Laves phase compounds CeFe2, CeRu2 and LaRu2 : an x-ray absorption spectroscopy (XAS) study

International Nuclear Information System (INIS)

Chaboy, J.; Garcia, J.; Marcelli, A.

1995-08-01

An x-ray absorption spectroscopy (XAS) investigation of the structural changes occurred upon hydriding in the Friauf-Laves phase compounds CeFe 2 , CeRu 2 and LaRu 2 compounds is presented. The analysis of the extended x-ray absorption spectroscopy (EXAFS) spectra at the L-edges of the rare-earth and at the Fe K-edge indicates that the hydrogenation process leads to the suppression of the long-range crystalline order in all the hydride derivates investigated, as well as the different influence of H 2 in both the rare earth and transition metal sublattices. The correlation between the structural and magnetic changes induced by the hydrogen in the lost matrix is discussed in terms of the modification of the electronic properties, i.e., intermediate-valence of Ce, and of the hybridization between the transition metal and rare-earth

Intermetallic phases in the iron-rich region of the Zr-Fe phase diagram

International Nuclear Information System (INIS)

Granovsky, M.S.; Arias, D.

1996-01-01

Intermetallic phases in the Fe-rich region of the Zr-Fe system are studied by X-ray diffraction and optical and electron microscopy. The chemical composition of each phase has been quantitatively measured in a electron microprobe. The stable phases found in this region are ZrFe 2 , Zr 6 Fe 23 and (αFe). ZrFe 2 is identified as a cubic Laves type phase (C15) and the ZrFe 2 /ZrFe 2 +Zr 6 Fe 23 boundary composition is 73±1 at.% Fe. Zr 6 Fe 23 is a cubic phase of the Th 6 Mn 23 type and its composition is 80.0±1.5 at.% Fe. The eutectic L↔Zr 6 Fe 23 +τ-Fe transformation temperature and composition are 1325 C and 91±1 at.% Fe, respectively. The solubility of Zr in τ-Fe at 1012 C is 500±50 appm and 1000±100 appm close to the eutectic temperature. (orig.)

Investigation on Long-term Creep Rupture Properties and Microstructure Stability of Fe-Ni based Alloy Ni-23Cr-7W at 700°C

DEFF Research Database (Denmark)

Tokairin, Tsuyoshi; Dahl, Kristian Vinter; Danielsen, Hilmar Kjartansson

2013-01-01

Long-term creep rupture properties and microstructural stability of Fe–Ni based alloy Ni–23Cr–7W (HR6W, ASME Code Case 2684) were experimentally investigated. Crept specimens at 700 °C for durations up to 37,667 h were chosen, the microstructure evolution during creep was characterized. Besides...... for the main strengthening precipitate, Laves phase. The alloy was proven to have good microstructural stability without observable coarsening of strengthening precipitates during long-term creep up to around 37,667 h. It was also verified that the growth kinetics of Laves phase can be well described...

Quasicrystalline and crystalline precipitation during isothermal tempering in a 12Cr-9Ni-4Mo maraging stainless steel

International Nuclear Information System (INIS)

Liu, P.; Stigenberg, A.H.; Nilsson, J.O.

1995-01-01

A thorough microstructural investigation has been performed on a high strength maraging steel of the type 12%Cr-9%Ni-4%Mo-2%Cu-1%Ti. The major precipitate formed during isothermal aging at 475 C is a quasicrystalline phase possessing icosahedral symmetry termed R'-phase with a typical chemical composition of 48%Mo-33%Fe-13%Cr-2%Ni-4%Si. At 550 C the major precipitate is trigonal R-phase with a typical composition of 45%Mo-31%Fe-18%Cr-4%Ni-2%Si. At 550 C also Laves phase with a composition of 48%Mo-35%Fe-13%Cr-2%Ni-2%Si could be observed. At both 475 and 550 C an ordered phase termed L-phase precipitated. This minority phase has an ordered face centered cubic (f.c.c.) structure of type L1 0 . Its composition is typically 9%Fe-4%Cr-52%Ni-15%Mo.-16%Ti-4%Al. R'-phase formed at 475 C transformed to R-phase and Laves phase during aging at 550 C. In an analogous manner, R-phase and Laves phase formed at 550 C transformed to R'-phase during subsequent aging at 475 C. This transformation was rationalized by a strong similarity in crystal structure between quasicrystalline R'-phase of icosahedral symmetry and Frank-Kasper phases such as R-phase and Laves phase

Bioconcentration of 14 C-Carbofuran and 14 C- Lindane in fresh water Tilapia Nilitica and the bioavailability of their residues to rats

International Nuclear Information System (INIS)

Aly, M.A.S.; Afifi, L.M.

1997-01-01

Tilapia Nilotica were exposed to 14 C- carbofuran (125 MUg/1) and 14 C - lindane (80 MUg/1) for 96 h. Uptake period followed by 8 days depuration period. The bioconcentration factor (BCF) for carbofuran reached 32.4 at 12 h and 82 for lindane at 48 h. The amount of 14 C-activity found in fish treated with 14 C - carbofuran after the uptake period showed the following descending order: viscera > remaining parts > gills > muscles. In case of 14 C - lindane treated fish the recovered amount followed the order; remaining parts> viscera > gills muscles. During the depuration period, carbofuran residues taken up by fish were eliminated in 2 phases, an initial rapid phase followed by a slower gradual one. However, the rate of elimination in case of lindane was much slower especially during the first 2 days. At the end of the depuration period (8 days), the muscles (edible portion) contained 10% and 58% of 14 C -activity in case of carbofuran and lindane treated groups, respectively. Both insecticides proved to be bioavailable when rats were fed treated fish. Of the administered dose, 44.1% and 53.0% were excreted in urine and feces case of 14 C-carbofuran while in case of 14 C - lindane it was 30.9% and 41.7% for urine and feces, respectively. 2 figs., 2 tabs

Behaviors of 14C-butachlor, 14C-chlorpyrifos and 14C-DDT in Rana japonica japonica Guenther

International Nuclear Information System (INIS)

Zhang Yiqiang; Zhong Chuangguang; Zhao Xiaokui; Chen Shunhua

2002-01-01

The research on the behaviors of 14 C-butachlor, 14 C-chlorpyrifos and 14 C-DDT in the frog Rana japonica japonica Guenther was carried out. After administrated per os to the frogs in doses of 380, 347, 363 Bq/g, 14 C-butachlor, 14 C-chlorpyrifos and 14 C-DDT, were distributed respectively to various organs within 24 h with specific accumulating organs as gallbladder, intestine and intestine, relevantly to the pesticides described. Compared to that in gallbladder and intestine, the radioactivity of many organs was extremely low, and this might due to the characters of the pesticides. Analysis of the metabolites of 14 C-DDT in frog at 24 th hr demonstrated that DDT was difficult to be degraded. Most 14 C-butachlor, 14 C-chlorpyrifos 14 C-DDT in liver and fat or ovary of frog was extractable with acetone. However, there were some differences between the pesticides, and the organs as well. And 14 C-butachlor, 14 C-chlorpyrifos or 14 C-DDT were better bound in liver than in fat

Structure and hydrogen storage properties of the hexagonal Laves phase Sc(Al{sub 1-x}Ni{sub x}){sub 2}

Energy Technology Data Exchange (ETDEWEB)

Sahlberg, Martin, E-mail: Martin.sahlberg@kemi.uu.se [Department of Chemistry, The Angstroem Laboratory, Uppsala University, Box 538, SE-751 21 Uppsala (Sweden); Angstroem, Jonas, E-mail: jonas.angstrom@kemi.uu.se [Department of Chemistry, The Angstroem Laboratory, Uppsala University, Box 538, SE-751 21 Uppsala (Sweden); Zlotea, Claudia, E-mail: claudia.zlotea@icmpe.cnrs.fr [Chimie Metallurgique des Terres Rares, Institut de Chimie et des Materiaux de Paris Est, UMR 7182, CNRS, 2-8 rue Henri Dunant, 94320 Thiais Cedex (France); Beran, Premysl, E-mail: pberan@ujf.cas.cz [Nuclear Physics Institute, Academy of Sciences of the Czech Republic, 25068 Rez (Czech Republic); Latroche, Michel, E-mail: michel.latroche@glvt-cnrs.fr [Chimie Metallurgique des Terres Rares, Institut de Chimie et des Materiaux de Paris Est, UMR 7182, CNRS, 2-8 rue Henri Dunant, 94320 Thiais Cedex (France); Pay Gomez, Cesar, E-mail: Cesar.paygomez@kemi.uu.se [Department of Chemistry, The Angstroem Laboratory, Uppsala University, Box 538, SE-751 21 Uppsala (Sweden)

2012-12-15

The crystal structures of hydrogenated and unhydrogenated Sc(Al{sub 1-x}Ni{sub x}){sub 2} Laves phases have been studied by combining several diffraction techniques and it is shown that hydrogen is situated interstitially in the A{sub 2}B{sub 2}-sites, which have the maximum number of scandium neighbours. The hydrogen absorption/desorption behaviour has also been investigated. It is shown that a solid solution of hydrogen forms in the mother compound. The hydrogen storage capacity exceeds 1.7 H/f.u. at 374 K, and the activation energy of hydrogen desorption was determined to 4.6 kJ/mol H{sub 2}. It is shown that these compounds share the same local coordination as Frank-Kasper-type approximants and quasicrystals, which opens up the possibility of finding many new hydride phases with these types of crystal structures. - Graphical abstract: The structure of ScNiAlDx, Sc atoms are shown in purple and Ni/Al atoms in blue and the iso-surfaces of deuterium in yellow. Revealed from refinements of neutron powder diffraction data. Highlights: Black-Right-Pointing-Pointer The crystal structure of ScNiAl and ScNiAlDx is reported. Black-Right-Pointing-Pointer We show the hydrogen storage properties of Sc(Al{sub 1-x}Ni{sub x}){sub 2}. Black-Right-Pointing-Pointer We discuss the possibility to store hydrogen in quasicrystals.

Microstructural evolution of ASTM P91 after 100,000 hours exposure at 550 C and 600 C

Energy Technology Data Exchange (ETDEWEB)

Cipolla, L.; Venditti, D.; Di Gianfrancesco, A. [Centro Sviluppo Materiali SpA, Rome (Italy); Caminada, S. [TenarisDalmine, Dalmine (Italy); Danielsen, H.K. [Technical Univ. of Denmark, Lyngby (Denmark)

2010-07-01

ASTM A335 P91 samples were investigated after creep testing at 550 C and 600 C for over 10{sup 5} h. X-Ray Diffraction, Scanning and Transmission Electron Microscopy were adopted to assess the microstructural evolution of the material in terms of precipitation changes during high temperature exposure. Mean equivalent diameters and average chemical compositions of MX and M{sub 23}C{sub 6} precipitates and Laves phases were assessed through the analysis of a large number of particles. Their growth and coarsening kinetics were determined at 600 C on many samples with increasing exposure times up to 100,000 hours. Also the presence of modified Z-phase, Cr(V, Nb)N, was investigated. The high microstructural stability of Grade 91 is related to the presence of fine and distributed MX carbonitrides, always present even after very long term temperature exposure. The mean size of MX carbonitrides remains almost constant and stays below 45 nm after 10{sup 5} h at 600 C. Although MX particles exhibit a Cr enrichment with increasing ageing times, indicating that they are absorbing Cr atoms from the surrounding matrix, their transformation into Z-phase is still at a very preliminary stage: only a few hybrid MX/Z particles and a few Z-phase precipitates were identified in the most aged sample after 10{sup 5} at 600 C. Coarsening of M{sub 23}C{sub 6} occurs during thermal exposure, but their average equivalent diameter, initially of 140 nm in the as-treated material, remains below 200 nm after 10{sup 5} h at 600 C. Laves particles form at grain boundaries after a relatively short time and soon become the largest precipitates. (orig.)

Effects of Nd-addition on the structural, hydrogen storage, and electrochemical properties of C14 metal hydride alloys

Energy Technology Data Exchange (ETDEWEB)

Wong, D.F. [BASF/Battery Materials-Ovonic, 2983 Waterview Drive, Rochester Hills, MI 48309 (United States); Department of Chemical Engineering, Wayne State University, Detroit, MI 48202 (United States); Young, K., E-mail: kwo.young@basf.com [BASF/Battery Materials-Ovonic, 2983 Waterview Drive, Rochester Hills, MI 48309 (United States); Department of Chemical Engineering, Wayne State University, Detroit, MI 48202 (United States); Nei, J.; Wang, L. [BASF/Battery Materials-Ovonic, 2983 Waterview Drive, Rochester Hills, MI 48309 (United States); Ng, K.Y.S. [Department of Chemical Engineering, Wayne State University, Detroit, MI 48202 (United States)

2015-10-25

Nd-addition to the AB{sub 2}-based alloy Ti{sub 12}Zr{sub 22.8−x}V{sub 10}Cr{sub 7.5}Mn{sub 8.1}Co{sub 7.0}Ni{sub 32.2}Al{sub 0.4}Nd{sub x} is studied for its effects on the structure, gaseous-phase hydrogen storage, and electrochemical properties. This study follows a series of Cu, Mo, Fe, Y, Si, and La doping studies in similar AB{sub 2}-based alloys. Limited solubility of Nd in the main Laves phase promotes the formation of secondary phases (AB and Zr{sub 7}Ni{sub 10}) to provide catalytic effects and synergies for improved capacity and high-rate dischargeability (HRD) performance. The main C14 storage phase has smaller lattice constants and cell volumes, and these effects reduce the storage capacity at higher Nd levels. Different hydrogen absorption mechanisms can occur in these multi-component, multi-phase alloys depending on the interfaces of the phases, and they have effects on the alloy properties. Higher Nd-levels improve the HRD performance despite having lower bulk diffusion and surface exchange current. Magnetic susceptibility measurements indicate large percentage of larger metallic nickel clusters are present in the surface oxide of alloys with higher Nd-content, and AC impedance studies show very low charge-transfer resistance with high catalytic capability in the alloys. The −40 °C charge-transfer resistance of 8.9 Ω g in this Nd-series of alloys is the lowest measured out of the studies investigating doped AB{sub 2}-based MH alloys for improved low-temperature characteristics. The improvement in HRD and low-temperature performance appears to be related to the proportion of the highly catalytic NdNi-phase at the surface, which must offset the increased bulk diffusion resistance in the alloy. - Graphical abstract: Schematics of hydrogen flow and corresponding PCT isotherms in funneling mode. - Highlights: • Structural and hydrogen storage properties of Nd-substituted AB{sub 2} metal hydride are reported. • Nd contributes to the lowest

On the crystallography and composition of topologically close-packed phases in ATI 718Plus®

International Nuclear Information System (INIS)

Krakow, Robert; Johnstone, Duncan N.; Eggeman, Alexander S.; Hünert, Daniela; Hardy, Mark C.; Rae, Catherine M.F.; Midgley, Paul A.

2017-01-01

ATI 718Plus ® is a nickel-based superalloy developed to replace Inconel 718 in aero engines for static and rotating applications. Here, the long-term stability of the alloy was studied and it was found that topologically close-packed (TCP) phases can form at the γ-η interface or, less frequently, at grain boundaries. Conventional and scanning transmission electron microscopy techniques were applied to elucidate the crystal structure and composition of these TCP precipitates. The precipitates were found to be tetragonal sigma phase and hexagonal C14 Laves phase, both being enriched in Cr, Co, Fe and Mo though sigma has a higher Cr and lower Nb content. The precipitates were observed to be heavily faulted along multiple planes. In addition, the disorientations between the TCP phases and neighbouring η/γ were determined using scanning precession electron diffraction and evaluated in axis-angle space. This work therefore provides a series of compositional and crystallographic insights that may be used to guide future alloy design.

Synthesis of [3-14C]- and [phenyl-U-14C] olaquindox

International Nuclear Information System (INIS)

Maul, W.; Scherling, D.; Seng, F.

1981-01-01

Olaquindox is a new feed additive. [ 14 C]Olaquindox, labelled in different positions, was needed for tracer-studies of pharmacokinetics, biotransformation and residues in several species of animals. 2-[N-(2-hydroxethyl)-carbamoyl]-3-methyl-[3- 14 C]quinoxaline-1,4-dioxide([3- 14 C]Olaquindox) was synthesized from barium[ 14 C]carbonate (22 mmoles; 1.15 Ci) via [1- 14 C]acetic acid, sodium[1- 14 C]acetate, [1- 14 C]acetylchloride, ethyl[3- 14 C]acetoacetate and 2-carbethoxy-3-methyl-[3- 14 C]quinoxaline-1,4-dioxide with an overall yield of 10%, based on barium[ 14 C]carbonate. The radiochemical purity was better than 98% (tlc). The specific activities of three preparations were 10.5, 8.4 and 5.45 μCi/mg respectively. [phenyl-U- 14 C]Olaquindox was synthesized starting from [U- 14 C]aniline (19.8 mmoles; 284.4 mCi). Intermediate products were N-acetyl[U- 14 C]aniline, 2-nitro-N-acetyl[U- 14 C]aniline, 2-nitro[U- 14 C]aniline and [U- 14 C]benzofurazanoxide. The total yield was 50% as calculated for [U- 14 C]aniline. At calibration samples of two preparations showed specific activities of 49.5 and 11.1 μCi/mg respectively. The radiochemical purity was checked by tlc and exceeded 98%. (author)

Studies on 14C-extractable residue, 14C-bound residue and mineralization of 14C-labeled chlorsulfuron in soils

International Nuclear Information System (INIS)

Ye Qingfu; Sun Jinhe; Qi Wenyuan; Wu Jianmin

2003-01-01

The purpose of the present study was to investigate 14 C-extractable residue ( 14 C-ER), 14 C-bound residue ( 14 C-BR) and mineralization of 14 C-labeled chlorsulfuron in soils by using isotope technique. The main factors affecting 14 C-BR formation and the distribution pattern of 14 C-BR in humus were also discussed in details. The results were as follows: (1) The 14 C-ER content of 14 C-chlorsulfuron in seven kinds of soil was positively related to soil pH and negatively related to clay content and organic matter content significantly. Moreover. the decrease rate of 14 C-chlorsulfuron parent compound derived from 14 C-ER in soils followed the first order rate reaction, the half-life in Soil 1-Soil 7 were 13.0, 13.1, 17.7, 133.3, 21.8, 22.1, 33.2 days, respectively. It was concluded that soil pH was the main factor affecting the degradation of 14 C-chlorsulfuron. (2) The 14 C-BR content of 14 C-chlorsulfuron in soils increased sharply with the incubation time during the initial 20 days, then changed slowly with time. However, 14 C-BR content during the whole incubation depended on soil types. The order of 14 C-BR content followed Soil 1 > Soil 2, Soil 5 and Soil 6 > Soil 3 > Soil 7 > Soil 4. The maximum values of 14 C-BR content of 14 C-chlorsulfuron in Soil 1-Soil 7 were 53.3%, 40.9%, 37.8%, 16.4%, 42.5%, 41.0% and 31.3% of applied amount. In addition, the 14 C-BR content of 14 C-chlorsulfuron in soils was negatively related to soil pH significantly, and positively related to the clay content. The soil pH was found to be the main factor affecting BR formation of 14 C-chlorsulfuron among the basic properties of soil. (3) During the whole periods of the incubation, the 14 C-BR of 14 C-chlorsulfuron in soils was mainly distributed in fulvic acid and humin. The relative percent of 14 C-BR in fulvic acid was higher than in humin. While the relative percentage of the 14 C-BR in humic acid only account for 2%. It was suggested that fulvic acid played an important role

Intermetallic phases in the iron-rich region of the Zr-Fe phase diagram

Energy Technology Data Exchange (ETDEWEB)

Granovsky, M.S. [Comision Nacional de Energia Atomica, Buenos Aires (Argentina). Dept. de Materiales; Arias, D. [Comision Nacional de Energia Atomica, Buenos Aires (Argentina). Dept. de Materiales

1996-04-01

Intermetallic phases in the Fe-rich region of the Zr-Fe system are studied by X-ray diffraction and optical and electron microscopy. The chemical composition of each phase has been quantitatively measured in a electron microprobe. The stable phases found in this region are ZrFe{sub 2}, Zr{sub 6}Fe{sub 23} and ({alpha}Fe). ZrFe{sub 2} is identified as a cubic Laves type phase (C15) and the ZrFe{sub 2}/ZrFe{sub 2}+Zr{sub 6}Fe{sub 23} boundary composition is 73{+-}1 at.% Fe. Zr{sub 6}Fe{sub 23} is a cubic phase of the Th{sub 6}Mn{sub 23} type and its composition is 80.0{+-}1.5 at.% Fe. The eutectic L{r_reversible}Zr{sub 6}Fe{sub 23}+{tau}-Fe transformation temperature and composition are 1325 C and 91{+-}1 at.% Fe, respectively. The solubility of Zr in {tau}-Fe at 1012 C is 500{+-}50 appm and 1000{+-}100 appm close to the eutectic temperature. (orig.).

Order-disorder phase transition in ZrV2Dsub(3.6)

International Nuclear Information System (INIS)

Didisheim, J.-J.; Yvon, K.; Tissot, P.

1981-01-01

The deuterated C15-type Laves phase ZrV 2 Dsub(3.6) undergoes a structural phase transition near room temperature (T of the order of 325 K). In the cubic high-temperature phase the deuterium atoms are disordered over two types of tetrahedral interstices, the centres of which are 1.3 A apart. In the tetragonal low-temperature phase the D atoms are ordered and occupy only the energetically more favourable interstices. The tetragonal structure is isotypic with the low-temperature phase of HfV 2 D 4 . The shortest D-D distance is 2.1 A. (author)

Experimental investigation of the Zr corner of the ternary Zr-Nb-Fe phase diagram

Energy Technology Data Exchange (ETDEWEB)

Granovsky, M.S. E-mail: granovsk@cnea.gov.ar; Canay, M.; Lena, E.; Arias, D

2002-04-01

Intermediate phases in the Zr-rich region of the Zr-Nb-Fe system have been investigated by X-ray diffraction, optical and electron microscopy and electron microprobe analysis. The chemical composition ranges covered by the alloys studied here are: (41-97) at.% Zr, (32-0.9) at.% Nb and (0.6-38) at.% Fe. The phases found in this region were: the solid solutions {alpha}-Zr and {beta}-Zr, the intermetallic Zr{sub 3}Fe with less than 0.2 at.% Nb in solution, two new ternary intermetallic compounds (Zr+Nb){sub 2}Fe '{lambda}{sub 1}' with a cubic Ti{sub 2}Ni-type structure in the composition range (2.4-13) at.% Nb and (31-33) at.% Fe, and (Fe+Nb){sub 2}Zr '{lambda}{sub 2}' indexed as hexagonal Laves phase MgZn{sub 2} type (C14) with a wide range of compositions close to (35-37) at.% Zr, (12-31) at.% Nb and (32-53) at.% Fe.

Experimental investigation of the Zr corner of the ternary Zr-Nb-Fe phase diagram

International Nuclear Information System (INIS)

Granovsky, M.S.; Canay, M.; Lena, E.; Arias, D.

2002-01-01

Intermediate phases in the Zr-rich region of the Zr-Nb-Fe system have been investigated by X-ray diffraction, optical and electron microscopy and electron microprobe analysis. The chemical composition ranges covered by the alloys studied here are: (41-97) at.% Zr, (32-0.9) at.% Nb and (0.6-38) at.% Fe. The phases found in this region were: the solid solutions α-Zr and β-Zr, the intermetallic Zr 3 Fe with less than 0.2 at.% Nb in solution, two new ternary intermetallic compounds (Zr+Nb) 2 Fe 'λ 1 ' with a cubic Ti 2 Ni-type structure in the composition range (2.4-13) at.% Nb and (31-33) at.% Fe, and (Fe+Nb) 2 Zr 'λ 2 ' indexed as hexagonal Laves phase MgZn 2 type (C14) with a wide range of compositions close to (35-37) at.% Zr, (12-31) at.% Nb and (32-53) at.% Fe

Placental transfer of 14C-hexoprenaline

International Nuclear Information System (INIS)

Lipshitz, J.; Broyles, K.; Whybrew, W.D.; Ahokas, R.A.; Anderson, G.D.

1982-01-01

The placental transfer of a single intravenous injection of 14 C-hexoprenaline was studied in eight pregnant New Zealand white rabbits. Maternal and fetal blood was sampled intermittently for 60 minutes after the injection. An initial rapid decrease in the levels of 14 C-hexoprenaline in maternal blood was followed by a second slower phase, whereas fetal heart rate after the administration of a single maternal intravenous injection of hexoprenaline in the treatment of fetal distress is due to the action on the uterus and/or on maternal cardiovascular function, and not to direct stimulation of the fetus

Bioconversion of α-[14C]Zearalenol and β-[14C]Zearalenol into [14C]Zearalenone by Fusarium roseum Gibbosum

International Nuclear Information System (INIS)

Richardson, K.E.; Hagler, W.M. Jr.; Hamilton, P.B.

1984-01-01

Cultures of Fusarium roseum Gibbosum on rice were treated with [ 14 C]zearalenone, α-[ 14 C]zearalenol, or β-[ 14 C]zearalenol to determine whether a precursor-product relationship exists among these closely related fungal metabolites. Culture extracts were purified by silica gel column chromatography and fractionated by high-pressure liquid chromatography, and the level of radioactivity was determined. Within 7 days, the β-[ 14 C]zearalenol was converted to zearalenone, and no residual β-[ 14 C]zearalenol was detectable. Most of the α-[ 14 C]zearalenol added was also converted into zearalenone within 14 days. In cultures treated with [ 14 C]zearalenone, no radioactivity was noted in any other components

Microstructural characterization of second phases in X10CrMoVNb9-1 and 12CrMoWCuVNb steels after long steam exposure time at 550 C

International Nuclear Information System (INIS)

Rodak, Kinga; Hernas, Adam; Vodarek, Vlastimil

2015-01-01

Microstructural changes in high alloy (9-12% Cr) creep resistant martensitic X10CrMoVNb9-1 and 12CrMoW . CuVNb steels after 100 000 h of steam exposure at 550 C have been studied using scanning transmission electron microscopy. Precipitates were identified using electron diffraction patterns and energy dispersive X-ray spectroscopy analysis. After long time exposure, a significant coarsening of M 23 C 6 carbides, and intensive precipitation of the coarse Laves phase were observed. Moreover, in the 12CrMoW . CuVNb steel, a low amount of the modified Z-phase particles was detected. The microstructures of the X10Cr . MoVNb9-1 and 12CrMoWCuVNb steels after 100 000 h of exposure differ in several aspects.

Microstructural characterization of second phases in X10CrMoVNb9-1 and 12CrMoWCuVNb steels after long steam exposure time at 550 C

Energy Technology Data Exchange (ETDEWEB)

Rodak, Kinga; Hernas, Adam [Silesian Univ. of Technology, Inst. of Materials Science, Katowice (Poland); Vodarek, Vlastimil [VSB-Technical Univ. of Ostrava (Czech Republic)

2015-07-15

Microstructural changes in high alloy (9-12% Cr) creep resistant martensitic X10CrMoVNb9-1 and 12CrMoW . CuVNb steels after 100 000 h of steam exposure at 550 C have been studied using scanning transmission electron microscopy. Precipitates were identified using electron diffraction patterns and energy dispersive X-ray spectroscopy analysis. After long time exposure, a significant coarsening of M{sub 23}C{sub 6} carbides, and intensive precipitation of the coarse Laves phase were observed. Moreover, in the 12CrMoW . CuVNb steel, a low amount of the modified Z-phase particles was detected. The microstructures of the X10Cr . MoVNb9-1 and 12CrMoWCuVNb steels after 100 000 h of exposure differ in several aspects.

Formation of 14C-asparagine from 14C-precursor in mulberry leaves

International Nuclear Information System (INIS)

Yamashita, Tadaaki

1981-01-01

Since a remarkable accumulation of asparagine in the young leaves of mulberry has been observed, the formation of 14 C-asparagine from 14 C-labeled substrates in young leaves was examined in comparison with that in the mature leaves. 14 C-aspartic acid and 14 C-succinic acid expected as active precursors for asparagine biosynthesis, and 14 C-sucrose as respiratory substrates were fed respectively to the disks of young or mature leaves of mulberry. Although 14 C-succinic acid was actively converted to 14 C-asparagine, no significant amount of 14 C-asparagine was formed from 14 C-aspartic acid in two hours of feeding period. The rate of formation of 14 C-asparagine from 14 C-succinic acid in the mature leaves was slightly higher than that in the young leaves. Amino acids other than asparagine acquired 14 C from 14 C-labeled substrates were mainly aspartic acid, glutamic acid, alanine and ν-amino butyric acid in both of the leaves. Intending to accelerate the formation of asparagine in the leaves, ammonium ion was supplied to culturing solution as only source of nitrogen and plants were grown for two weeks in that solution before 14 C-labeled substrates feeding experiments. Supplying of ammonium ion brought about enhanced accumulation of asparagine in the young leaves, and caused remarkable formation of 14 C-asparagine from 14 C-aspartic acid in both of the leaves. However, the rate of 14 C-asparagine formation from 14 C-aspartic acid in the young leaves did not exceed that in the mature leaves. (author)

TEM characterization of microstructure evolution of 12%Cr heat resistant steels

Energy Technology Data Exchange (ETDEWEB)

Rojas, D.; Prat, O.; Sauthoff, G. [Max-Planck-Institut fuer Eisenforschung GmbH, Duesseldorf (Germany); Garcia, J. [Helmholtz-Zentrum Berlin fuer Materialien und Energie GmbH, Berlin (Germany); Kaysser-Pyzalla, A.R. [Helmholtz-Zentrum Berlin fuer Materialien und Energie GmbH, Berlin (Germany); Bochum Univ. (Germany)

2010-07-01

A detailed characterization of the microstructure evolution of 12%Cr heat resistant steels at different creep times (100 MPa / 650 C / 8000 h) were carried out by scanning transmission electron microscopy (STEM). The results of the microstructure analysis are correlated with the mechanical properties in order to investigate the influence of different precipitates (especially M{sub 23}C{sub 6}) on the creep strength of the alloys. Precipitation of Laves phase and Z-phase was observed after several hours creep time. Very few Z-phase of the type Cr(V,Ta)N nucleating from existing (V,Ta)(C,N) was observed. Both alloys show growth and coarsening of Laves phase, meanwhile the MX carbonitrides present a very slow growth and coarsening rate. Alloys containing Laves phase, MX and M{sub 23}C{sub 6} precipitates show best creep properties. (orig.)

Degradation of 14C-glyphosate in compost amended soils.

Science.gov (United States)

Alexa, E; Bragea, M; Sumalan, R; Negrea, M; Lazureanu, A

2009-01-01

Glyphosate (N-phosphonomethyl-glycine), the active ingredient in several herbicide formulations, is a non-selective, post-emergent herbicide used in a variety of crop and non-crop situations. Glyphosate is a non-volatile herbicide that is relatively immobile in soil. Its degradation is due to microbiological processes and most laboratory studies have been conducted with 14C-glyphosate with the rate of 14CO2 evolution being used as an indication of herbicide breakdown. In this paper we have studied the glyphosate degradation in compost amendment soils using Scientilator Liquid TRIATHLER and Glyphosate-phosphonomethyl-14C-labeled with specific activity 2,2mCi/mmol. Four types of soils have been taken under study: Black Chernozem, Vertisol, Gleysol and Phaeozem with different characteristics. For the each type of soil have been realized four experimental variants (glyphosate blind sample with 1,5 ppm, concentration, autoclaved soil, soil with glyphosate and addition of compost in field concentration of 40 t/ha, respectively 60 t/ha. The mineralization curves of 14CO2 accumulated were compared during of 40 days. All the mineralization curves for the soils exhibited same patterns, with only two phases, the initial rapid phase of degradation, for about 20 days, attributed to microbial action on the free glyphosate and the second slow phase, when the curves attained plateaus. Compost applied with different concentrations to Vertisol and Black Chernozem did not appear to stimulate the microbial degradation of glyphosate. In Gleysol and Phaeozem with lower humus content, the mineralization curve of 14C indicate the increase degradation capacity, expressed as accumulated 14CO2 as % total 14C, with the increase of compost concentration.

Study of the reaction 14 C (p,p) 14 C

International Nuclear Information System (INIS)

Murillo, G.; Ramirez, J.; Avila, O.; Fernandez, M.; Darden, S.E.; Prior, R.P.; Sen, S.

1991-04-01

The study of the elastic scattering of polarized protons in 14 C, it has been very limited. Some angular distributions exists to low energy, as well as measures of excitation functions to several angles for the differential section and the vectorial analyzer power. A detailed study of the elastic scattering of protons by 14 C, it give us experimental information of the excited states in 15 N. The study of these states, is since of considerable interest it is not very easy to obtain a target of 14 C also in a reaction 14 C (p,p) 14 C is possible to obtain information of levels in 15 N to an excitation energy E X >14.95 MeV. (Author)

Placental transfer of 14C-hexoprenaline

International Nuclear Information System (INIS)

Lipshitz, J.; Broyles, K.; Whybrew, W.D.; Ahokas, R.A.; Anderson, G.D.

1982-01-01

The placental transfer of a single intravenous injection of 14C-hexoprenaline was studied in eight pregnant New Zealand white rabbits. Maternal and fetal blood was sampled intermittently for 60 minutes after the injection. An initial rapid decrease in the levels of 14C-hexoprenaline in maternal blood was followed by a second slower phase, whereas fetal levels remained insignificant. The conclusion, therefore, is that the rapid improvement in fetal heart rate after the administration of a single maternal intravenous injection of hexoprenaline in the treatment of fetal distress is due to the action on the uterus and/or on maternal cardiovascular function, and not to direct stimulation of the fetus

Convenient synthesis of [2-14C]-methylglyoxal bis(guanylhydrazone), [14C]-mitoguazone

International Nuclear Information System (INIS)

Burgos, A.; Ellames, G.J.

1995-01-01

[2- 14 C]-Methylglyoxal bis(guanylhydrazone) dihydrochloride, [ 14 C]-mitoguazone has been prepared in three steps from potassium[1- 14 C]-acetate in an overall radiochemical yield of 16%. The key steps in this procedure are the formation of the sodium salt of[acetone-2- 14 C]-methylsulfinylacetone, and Pummerer rearrangement to the [ 14 C] labelled hermithioacetal, which is trapped with two equivalents of aminoguanidine to afford the desired [ 14 C]-mitoguazone. (Author)

Elastic constants of a Laves phase compound: C15 NbCr2

International Nuclear Information System (INIS)

Ormeci, A.; Chu, F.; Wills, J.M.; Chen, S.P.; Albers, R.C.; Thoma, D.J.; Mitchell, T.E.

1997-01-01

The single-crystal elastic constants of C15 NbCr 2 have been computed by using a first-principles, self-consistent, full-potential total energy method. From these single-crystal elastic constants the isotropic elastic moduli are calculated using the Voigt and Reuss averages. The calculated values are in fair agreement with the experimental values. The implications of the results are discussed with regards to Poisson's ratio and the direction dependence of Young's modulus

Investigation Of Temperature Dependent Characteristics Of ...

African Journals Online (AJOL)

The structure, magnetization and magnetostriction of Laves phase compound TbCo2 were investigated by temperature dependent high resolution neutron powder diffraction. The compound crystallizes in the cubic Laves phase C15 structure above its Curie temperature, TC and exhibits a rhombohedral distortion (space ...

Effect of Ti/Cr content on the microstructures and hydrogen storage properties of Laves phase-related body-centered-cubic solid solution alloys

Energy Technology Data Exchange (ETDEWEB)

Young, K., E-mail: kwo.young@basf.com [BASF/Battery Materials-Ovonic, 2983 Waterview Drive, Rochester Hills, MI 48309 (United States); Wong, D.F. [BASF/Battery Materials-Ovonic, 2983 Waterview Drive, Rochester Hills, MI 48309 (United States); Department of Chemical Engineering and Materials Science, Wayne State University, MI 48202 (United States); Wang, L. [BASF/Battery Materials-Ovonic, 2983 Waterview Drive, Rochester Hills, MI 48309 (United States)

2015-02-15

Highlights: • Influences of Ti/Cr to BCC to hydrogen storage properties were reported. • A new activation using hydrogen pressure at 5 MPa was developed. • A discharge capacity of 463 mA h g{sup −1} was reported on a C14(36%)/BCC(64%) alloy. • Increase in Ti/Cr increases storage capacity and decreases high-rate performance. • The high-rate performance was dominated by the surface reaction. - Abstract: A series of BCC/C14 mixed phase alloys with the chemical composition of Ti{sub 13.6+x}Zr{sub 2.1}V{sub 44}Cr{sub 13.2−x}Mn{sub 6.9}Fe{sub 2.7}Co{sub 1.4}Ni{sub 15.7}Al{sub 0.3}, x = 0, 2, 4, 6, 8, 10, and 12, was fabricated, and their structural, gaseous phase and electrochemical hydrogen storage properties were studied. Raising the maximum pressure for measuring the gaseous hydrogen storage capacity allowed these alloys to reach full activation, and the maximum discharge capacities ranged from 375 to 463 mA h g{sup −1}. As the Ti/Cr ratio in the alloy composition increased, the maximum gaseous hydrogen storage capacity improved due to the expansion in both BCC and C14 unit cells. However, reversibility decreased due to the higher stability of the hydride phase, as indicated by the lower equilibrium pressures measured for these alloys. As with most other metal hydride alloys, the electrochemical capacities measured at 50 and 4 mA g{sup −1} fell between the boundaries set by the maximum and reversible gaseous hydrogen storage capacities. The poorer high-rate dischargeability observed with higher Ti/Cr ratios was attributed to the lower surface exchange current (less catalytic). Two other negative impacts observed with higher Ti/Cr ratios in the alloy composition are poorer cycle stability and lower open-circuit voltage.

Photo-Induced Phase Transitions to Liquid Crystal Phases: Influence of the Chain Length from C8E4 to C14E4

Directory of Open Access Journals (Sweden)

Simone Techert

2009-09-01

Full Text Available Photo-induced phase transitions are characterized by the transformation from phase A to phase B through the absorption of photons. We have investigated the mechanism of the photo-induced phase transitions of four different ternary systems CiE4/alkane (i with n = 8, 10, 12, 14; cyclohexane/H2O. We were interested in understanding the effect of chain length increase on the dynamics of transformation from the microemulsion phase to the liquid crystal phase. Applying light pump (pulse/x-ray probe (pulse techniques, we could demonstrate that entropy and diffusion control are the driving forces for the kind of phase transition investigated.

Last fra kornede materialer på begrænsningsvægge i lave lagerbygninger

DEFF Research Database (Denmark)

Møller, S.

Rapporten indeholder forudsætninger og retningslinier for den statiske beregning af lave lagerbygninger, fx. plansiloer i landbruget. I to hovedkapitler gives data og formler til lastbestemmelse som grundlag for brudundersøgelse og deformationsundersøgelse, samt et eksempel på lastberegning....

Percutaneous absorption of [14C]DDT and [14C]benzo[a]pyrene from soil

International Nuclear Information System (INIS)

Wester, R.C.; Maibach, H.I.; Bucks, D.A.; Sedik, L.; Melendres, J.; Liao, C.; DiZio, S.

1990-01-01

The objective was to determine percutaneous absorption of DDT and benzo[a]pyrene in vitro and in vivo from soil into and through skin. Soil (Yolo County 65-California-57-8; 26% sand, 26% clay, 48% silt) was passed through 10-, 20-, and 48-mesh sieves. Soil then retained by 80-mesh was mixed with [14C]-labeled chemical at 10 ppm. Acetone solutions at 10 ppm were prepared for comparative analysis. Human cadaver skin was dermatomed to 500 microns and used in glass diffusion cells with human plasma as the receptor fluid (3 ml/hr flow rate) for a 24-hr skin application time. With acetone vehicle, DDT (18.1 +/- 13.4%) readily penetrated into human skin. Significantly less DDT (1.0 +/- 0.7%) penetrated into human skin from soil. DDT would not partition from human skin into human plasma in the receptor phase (less than 0.1%). With acetone vehicle, benzo[a]pyrene (23.7 +/- 9.7%) readily penetrated into human skin. Significantly less benzo[a]pyrene (1.4 +/- 0.9%) penetrated into human skin from soil. Benzo[a]pyrene would not partition from human skin into human plasma in the receptor phase (less than 0.1%). Substantivity (skin retention) was investigated by applying 14C-labeled chemical to human skin in vitro for only 25 min. After soap and water wash, 16.7 +/- 13.2% of DDT applied in acetone remained absorbed to skin. With soil only 0.25 +/- 0.11% of DDT remained absorbed to skin. After soap and water wash 5.1 +/- 2.1% of benzo[a]pyrene applied in acetone remained absorbed to skin. With soil only 0.14 +/- 0.13% of benzo[a]pyrene remained absorbed to skin

Determination of the hydrothermal degradation products of D-(U-14C) glucose and D-(U-14C) fructose by TLC

International Nuclear Information System (INIS)

Bonn, G.; Bobleter, O.

1983-01-01

Hydrothermal degradation was examined using D-(U- 14 C) glucose and D-(U- 14 C) fructose. By thin layer chromatography with methylene chloride, tetrahydrofuran (THF), acetic acid - 60:20:20 as a mobile phase; it was possible to separate and identify the carbohydrates and their reaction products, glyceraldehyde, dihydroxyacetone, methylglyoxal, glycolaldehyde, 5-hydroxymethylfurfural and furfural. Up to 99% of the initial activity was determined by scintillation counting of the TL-chromatograms. A reaction scheme for the hydrothermal degradation of glucose and fructose was obtained from these results. (author)

14C and 13C in the atmosphere and soil air at two localities of Slovakia

International Nuclear Information System (INIS)

Sivo, A.; Simon, J.; Richtarikova, M.; Holy, K.; Polaskova, A.; Bulko, M.; Hola, O.

2006-01-01

In this paper there are presented the long-term measurements of 13 R and 14 R in urban and countryside atmosphere. The different conditions and particularities of both the localities which influence on the mentioned characteristics are pointed out. The existence of δ 13 C and δ 14 C variations and their phase correlation were confirmed as well as their origin were qualitatively explained. By means of the non-linear regression and harmonic analysis the trends of δ 13 C and δ 14 C variations was found. The study of δ 13 C and δ 14 C courses has shown that it can be used as an effective tool to determine the level of the anthropogenic CO 2 pollution of the atmosphere. (authors)

Phase Composition of a CrMo0.5NbTa0.5TiZr High Entropy Alloy: Comparison of Experimental and Simulated Data

OpenAIRE

Fan Zhang; Oleg N. Senkov; Jonathan D. Miller

2013-01-01

Microstructure and phase composition of a CrMo0.5NbTa0.5TiZr high entropy alloy were studied in the as-solidified and heat treated conditions. In the as-solidified condition, the alloy consisted of two disordered BCC phases and an ordered cubic Laves phase. The BCC1 phase solidified in the form of dendrites enriched with Mo, Ta and Nb, and its volume fraction was 42%. The BCC2 and Laves phases solidified by the eutectic-type reaction, and their volume fractions were 27% and 31%, respectively....

Preparative isolation of [U-14C]solanesol from 14CO2-chamber grown tobacco

International Nuclear Information System (INIS)

Hassam, S.B.

1985-01-01

A method for the preparative isolation of [U- 14 C]solanesol from 14 CO 2 -chamber grown tobacco is described. Freeze-dried tobacco leaves were Soxhlet extracted with methylene chloride. Fractionation of the extract by silica gel chromatography yielded crude solanesol. Subsequent purification by normal phase high pressure liquid chromatography yielded [U- 14 C]solanesol with a total activity of 474 μCi, a specific activity of 0.5 mCi/mmol, and a radiochemical purity of 95% as determined by RP-HPLC. The chemical purity was 97% and the chemical identity of the isolated compound was confirmed by co-chromatography with reference material and by mass spectroscopy. (author)

The liquidus surface of the Cr–Al–Nb system and re-investigation of the Cr–Nb and Al–Cr phase diagrams

International Nuclear Information System (INIS)

Stein, F.; He, C.; Wossack, I.

2014-01-01

Highlights: • Liquidus surface and reaction scheme of the Cr–Al–Nb system experimentally determined. • Solidification paths of the ternary alloys derived from as-cast microstructures. • Compositions and temperatures of the invariant points. • Revised versions of the phase diagrams of the Cr–Nb and Al–Cr boundary systems. - Abstract: The liquidus surface and corresponding reaction scheme of the ternary Cr–Al–Nb system were determined experimentally. The solidification paths of a series of more than 40 ternary alloys were deduced from investigation of their as-cast microstructures and measurement of all reaction temperatures applying scanning electron microscopy (SEM), electron probe microanalysis (EPMA), X-ray diffraction (XRD), and differential thermal analysis (DTA). The hexagonal C14-type Laves phase Nb(Cr,Al) 2 , which is not stable in any of the binary boundary systems and which is the only ternary compound, forms the most extended primary crystallization field of the ternary system dominating the centre of the liquidus surface. A ternary eutectic was found near the Al–Nb boundary composed of the three intermetallic phases C14 + Nb 2 Al + NbAl 3 . Besides the ternary liquidus surface, the solidus and liquidus curves of the Cr–Nb boundary system and of the Cr-rich part of the Al–Cr system were determined resulting in revised binary phase diagrams

C14 Assays and Autoradiographic Studies on the Rooster Comb

Science.gov (United States)

Balazs, Endre A.; Szirmai, John A.; Bergendahl, Gudrun

1959-01-01

The distribution of C14 was studied in various parts of the rooster comb following treatment with testosterone. The value of gas-phase assay of C14 in tissue has been demonstrated and the results compared with those of autoradiographic studies on the same tissue. The results of these experiments showed that androgen treatment significantly increases the rate of incorporation of C14 in various parts of the comb. The specific activity of carbon in the comb, cornea, and liver differed, depending on which precursor, viz. glucose-6-C14, glucose-1-C14, and glucuronolactone-U-C14, was administered. The highest values were obtained after the administration of glucose-6-C14; glucuronolactone-U-C14 gave the lowest specific activity. The specific activity of carbon in different parts of the comb showed considerable variation. Carbon assay of serial sections of the comb cut at various planes showed that the specific activity of carbon was highest in the mucoid layer. Both C14 assays and autoradiograms indicate that C14 is also present in other parts of the comb. As seen in autoradiography, the concentration of C14 was highest in the epithelium, in the blood vessel walls, and in the avascular collagenous tissue. These results, and indications from previous studies, suggest that the high specific activity of carbon in the mucoid layer is due mainly to the presence of C14-labelled hyaluronic acid. Autoradiograms and PAS staining suggest that a significant amount of C14 is also incorporated into the glycoproteins associated with the collagen fibers. PMID:13654453

A convenient synthesis of sup 14 C-cotinine from sup 14 C-nicotine

Energy Technology Data Exchange (ETDEWEB)

Desai, D.H.; Djordjevic, M.V.; Amin, S. (American Health Foundation, Valhalla, NY (USA). Naylor Dana Inst. for Disease Prevention)

1991-03-01

A convenient synthesis with analytical monitoring of {sup 14}C-cotinine is reported. {sup 14}C-Nicotine was converted into {sup 14}C-dibromocotinine hydrobromide perbromide. Debromination, achieved by using Zn dust/acetic acid, resulted in high yields (71%) of {sup 14}C-cotinine. (author).

Syntheses of [6-14C] and [5-carboxy, 6-14C2]nitrendipine

International Nuclear Information System (INIS)

Maul, N.; Scherling, D.

1989-01-01

[6- 14 C]Nitrendipine synthesis started from barium[ 14 ]carbonate, which was converted to [1- 14 C]acetyl chloride. The acid chloride was condensed with Meldrum's acid (2,2-dimethyl-1,3-dioxane-4,6-dione). The resulting intermediate was treated with boiling methanol to give methyl [3- 14 C]acetoacetate. The reaction with gaseous ammonia in toluene yielded the corresponding methyl 3-amino[3- 14 C]crotonate which was condensed with ethyl 2-(3-nitro-benzylidene) acetoacetate to obtain [6- 14 C]nitrendipine. (author)

9-12% Cr heat resistant steels. Alloy design, TEM characterisation of microstructure evolution and creep response at 650 C

International Nuclear Information System (INIS)

Rojas Jara, David

2011-01-01

This work was carried out aiming to design and characterise 9-12% Cr steels with tailormade microstructures for applications in fossil fuel fired power plants. The investigations concentrated in the design and characterisation of heat resistant steels for applications in high oxidising atmospheres (12% Cr) and 9% Cr alloys for components such as rotors (P91). ThermoCalc calculations showed to be a reliable tool for alloy development. The modeling also provided valuable information for the adjustment of the processing parameters (austenisation and tempering temperatures). Two 12% Cr heat resistant steels with a fine dispersion of nano precipitates were designed and produced supported by thermodynamic modeling (ThermoCalc). A detailed characterisation of the microstructure evolution at different creep times (100 MPa / 650 C / 8000 h) was carried out by scanning transmission electron microscopy (STEM). The results of the microstructure analysis were correlated with the mechanical properties in order to investigate the influence of different precipitates (especially M 23 C 6 carbides) on the creep strength of the alloys. Precipitation of Laves phase and Z-phase was observed after several hundred hours creep time. Very few Z-phase of the type Cr(V,Ta)N nucleating from existing (V,Ta)(C,N) was observed. Both alloys show growth and coarsening of Laves phase, meanwhile the MX carbonitrides present a very slow growth and coarsening rate. Alloys containing Laves phase, MX and M 23 C 6 precipitates show best creep properties. The influence of hot-deformation and tempering temperature on the microstructure evolution on one of the designed 12% Cr alloys was studied during short-term creep at 80-250 MPa and 650 C. Quantitative determination of dislocation density and sub-grain size in the initial microstructure and after creep was investigated by STEM combined with the high-angle annular dark-field detector (HAADF). A correlation between microstructure evolution and creep

9-12% Cr heat resistant steels. Alloy design, TEM characterisation of microstructure evolution and creep response at 650 C

Energy Technology Data Exchange (ETDEWEB)

Rojas Jara, David

2011-03-21

This work was carried out aiming to design and characterise 9-12% Cr steels with tailormade microstructures for applications in fossil fuel fired power plants. The investigations concentrated in the design and characterisation of heat resistant steels for applications in high oxidising atmospheres (12% Cr) and 9% Cr alloys for components such as rotors (P91). ThermoCalc calculations showed to be a reliable tool for alloy development. The modeling also provided valuable information for the adjustment of the processing parameters (austenisation and tempering temperatures). Two 12% Cr heat resistant steels with a fine dispersion of nano precipitates were designed and produced supported by thermodynamic modeling (ThermoCalc). A detailed characterisation of the microstructure evolution at different creep times (100 MPa / 650 C / 8000 h) was carried out by scanning transmission electron microscopy (STEM). The results of the microstructure analysis were correlated with the mechanical properties in order to investigate the influence of different precipitates (especially M{sub 23}C{sub 6} carbides) on the creep strength of the alloys. Precipitation of Laves phase and Z-phase was observed after several hundred hours creep time. Very few Z-phase of the type Cr(V,Ta)N nucleating from existing (V,Ta)(C,N) was observed. Both alloys show growth and coarsening of Laves phase, meanwhile the MX carbonitrides present a very slow growth and coarsening rate. Alloys containing Laves phase, MX and M{sub 23}C{sub 6} precipitates show best creep properties. The influence of hot-deformation and tempering temperature on the microstructure evolution on one of the designed 12% Cr alloys was studied during short-term creep at 80-250 MPa and 650 C. Quantitative determination of dislocation density and sub-grain size in the initial microstructure and after creep was investigated by STEM combined with the high-angle annular dark-field detector (HAADF). A correlation between microstructure

Microstructures and mechanical properties of two-phase alloys based on NbCr{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Chen, K.C.; Kotula, P.G.; Cady, C.M.; Mauro, M.E.; Thoma, D.J.

1999-07-01

A two-phase, NbCrTi alloy (bcc + C15 Laves phase) has been developed using several alloy design methodologies. In efforts to understand processing-microstructure-property relationships, different processing routes were employed. The resulting microstructures and mechanical properties are discussed and compared. Plasma arc melted (PAM) samples served to establish baseline, as-cast properties. In addition, a novel processing technique, involving decomposition of a supersaturated and metastable precursor phase during hot isostatic pressing (HIP), was used to produce a refined, equilibrium two-phase microstructure. Quasi-static compression tests as a function of temperature were performed on both alloy types. Different deformation mechanisms were encountered based upon temperature and microstructure.

Absorption, Distribution, Metabolism, and Excretion of [14C]-Volixibat in Healthy Men: Phase 1 Open-Label Study.

Science.gov (United States)

Siebers, Nicholas; Palmer, Melissa; Silberg, Debra G; Jennings, Lee; Bliss, Caleb; Martin, Patrick T

2018-02-01

Volixibat is a potent inhibitor of the apical sodium-dependent bile acid transporter in development for the treatment of nonalcoholic steatohepatitis. This phase 1, open-label study investigated the absorption, distribution, metabolism, and excretion of [ 14 C]-volixibat in heathy men. Eligible men (n = 8) aged 18-50 years (body mass index 18.0-30.0 kg/m 2 ; weight >50 kg) received a single oral dose of [ 14 C]-volixibat 50 mg containing ~5.95 µCi radioactivity. The primary objectives were to assess the pharmacokinetics of [ 14 C]-volixibat and to determine the total radioactivity in whole blood, plasma, urine, and feces at pre-selected time points over 6 days. The secondary objectives were to characterize metabolites and to assess the safety and tolerability. Low concentrations of volixibat (range 0-0.179 ng/mL) were detected in plasma up to 8 h following administration; the pharmacokinetic parameters could not be calculated. No radioactivity was observed in plasma or whole blood. The percentage (mean ± standard deviation) of total radioactivity in urine was 0.01 ± 0.007%. The vast majority (92.3 ± 5.25%) of volixibat was recovered in feces (69.2 ± 33.1% within 24 h). Unchanged volixibat was the only radioactive component detected in feces. Adverse events were mild in severity and mostly gastrointestinal. Changes in laboratory values were not clinically meaningful. Following oral administration, [ 14 C]-volixibat was excreted unchanged from the parent compound almost exclusively via fecal excretion, indicating that the drug is minimally absorbed. Consistent with other studies, adverse events were primarily gastrointestinal in nature. ClinicalTrials.gov identifier NCT02571192.

14C-labeled diesel exhaust particles: chemical characteristics and bioavailability studies

International Nuclear Information System (INIS)

Sun, J.D.; Wolff, R.K.; Dutcher, J.S.; Brooks, A.L.

1981-01-01

Little is known about the deposition, retention and biological fate of the organic compounds associated with diesel exhaust particles. In the studies reported here, a one-cylinder diesel engine was operated on diesel fuel spiked with 14 C-benzene, 14 C-hexadecane or 14 C-dotriacontane to generate 14 C-labeled diesel exhaust. Approximately 1% of the exhaust radioactivity was associated with the particulate phase of diesel exhaust. Chemical fractionation of the particle extract showed the 14 C to be present in each of the various chemical class fractions collected. Serum removed approx. 60% of the dichloromethane extractable radioactivity from these diesel particles while saline removed only approx. 6%. This suggested that the organic compounds may be removed from diesel particles in vivo. Future inhalation exposures of rodents to 14 C-labeled diesel exhausts are planned to gain additional information on the health risk of human exposure to diesel exhaust

Convenient synthesis of [2-{sup 14}C]-methylglyoxal bis(guanylhydrazone), [{sup 14}C]-mitoguazone

Energy Technology Data Exchange (ETDEWEB)

Burgos, A.; Ellames, G.J. [Sterling Winthrop Research Centre, Alnwick (United Kingdom). Pharmaceuticals Research Div.

1995-01-01

[2-{sup 14}C]-Methylglyoxal bis(guanylhydrazone) dihydrochloride, [{sup 14}C]-mitoguazone has been prepared in three steps from potassium[1-{sup 14}C]-acetate in an overall radiochemical yield of 16%. The key steps in this procedure are the formation of the sodium salt of[acetone-2-{sup 14}C]-methylsulfinylacetone, and Pummerer rearrangement to the [{sup 14}C] labelled hermithioacetal, which is trapped with two equivalents of aminoguanidine to afford the desired [{sup 14}C]-mitoguazone. (Author).

Elastic constants of the C15 laves phase compound NbCr2

International Nuclear Information System (INIS)

Chu, F.; He, Y.; Thoma, D.J.; Mitchell, T.E.

1995-01-01

Elastic properties of a solid are important because they relate to various fundamental solid-state phenomena such as interatomic potentials, equations of state, and phonon spectra. Elastic properties are also linked thermodynamically with specific heat, thermal expansion, Debye temperature, and Gruneisen parameter. Most important, knowledge of elastic constants is essential for many practical applications related to the mechanical properties of a solid as well: load-deflection, thermoelastic stress, internal strain (residual stress), sound velocities, dislocation core structure, and fracture toughness. In order to understand better the physical properties and deformation behavior of the C15 compound NbCr 2 , the authors have studied its elastic properties in this paper. In Section 2, the experimental methods are described, including the preparation of the sample and the measurement of the elastic constants. In Section 3, the experimental results are presented and the implications of these experimental results are discussed. Conclusions are drawn in Section 4

Processing ix spent resin waste for C-14 isotope recovery

International Nuclear Information System (INIS)

Chang, F. H.; Woodall, K. B.; Sood, S. K.; Vogt, H. K.; Krochmainek, L. S.

1991-01-01

-213 Ci/m 3 for the Moderator spent resins generated by CANDU reactors. For an estimated average C-14 activity level of 100 Ci/m 3 , a total of 400 Ci of C-14 can be produced each year. Based on the current market value of the C-14 isotope, the cost of the demonstration plant can be recovered in less than two years. Upon successful demonstration, the process can be scaled up. The volume of resin wastes produced by the stations can readily supply a full scale production of 2000 Ci or more per annum. Several alternative routes have been considered for this process which include: thermal stripping vs. acid stripping of the spent resins, laser enrichment vs. cryogenic distillation for the enrichment of the gaseous intermediate product, and direct gas phase reaction vs. liquid phase ionic precipitation of the final product. Analysis of the experimental results obtained at Ontario Hydro Research Division and also those reported in the literature has led to the selection of the following process: The C-14 is first removed by acid stripping the resins to form carbon dioxide. The gas is then separated from the carrier gas and converted by reaction with zinc to carbon monoxide, which is cryogenically distilled. Essentially pure C-14 monoxide is obtained and oxidized to produce C-14 dioxide. The gas is then reacted with a suitable hydroxide to produce the desired carbonate product

Elastic constants of a Laves phase compound: C15 NbCr{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Ormeci, A. [Koc Univ., Istanbul (Turkey)]|[Los Alamos National Lab., NM (United States); Chu, F.; Wills, J.M.; Chen, S.P.; Albers, R.C.; Thoma, D.J.; Mitchell, T.E. [Los Alamos National Lab., NM (United States)

1997-04-01

The single-crystal elastic constants of C15 NbCr{sub 2} have been computed by using a first-principles, self-consistent, full-potential total energy method. From these single-crystal elastic constants the isotropic elastic moduli are calculated using the Voigt and Reuss averages. The calculated values are in fair agreement with the experimental values. The implications of the results are discussed with regards to Poisson`s ratio and the direction dependence of Young`s modulus.

Application of Ab Initio Electronic Structure Calculations in Construction of Phase Diagrams of Metallic Systems with Complex Phases

Czech Academy of Sciences Publication Activity Database

Šob, Mojmír; Kroupa, Aleš; Pavlů, Jana; Vřešťál, Jan

2009-01-01

Roč. 150, č. 1 (2009), s. 1-28 ISSN 1012-0394 R&D Projects: GA MŠk OC 147; GA ČR GA106/07/1078 Institutional research plan: CEZ:AV0Z20410507 Keywords : Ab initio calculations * CALPHAD method * Laves phases * sigma phase * ternary systems * super-austenitic steels Subject RIV: BM - Solid Matter Physics ; Magnetism

Synthesis of 11-14C-quetiapine, 11-14C-isoclotiapine and 10-(4-methylpiperazin-1-yl)pyrido[4,3-b][1,4]benzothiazepine[10-14C

International Nuclear Information System (INIS)

Naghi Saadatjoo; Mohsen Javaheri; Nuclear Science and Technology Research Institute, Tehran; Nader Saemian; Mohsen Amini

2016-01-01

Quetiapine is one of the most widely used antipsychotic drug which acts as an antagonist for multiple neurotransmitter receptor sites. 2-[2-(4-(Dibenzo[b,f][1,4]thiazepin-11-yl)piperazin-1-yl)ethoxy]ethanol (quetiapine) labeled with carbon-14 in 11-position has been synthesized as part of a 5-step sequence from anthranilic acid-[carboxy- 14 C]. We have presented a convenient synthetic pathway for labeling of quetiapine with carbon-14 by using one-pot procedures from a key thiazepin-11(10H)-one-[11- 14 C] by good radiochemical yield. And also isoclotiapine[11- 14 C], and 10-(4-methylpiperazin-1-yl)pyrido[4,3-b][1,4]benzothiazepine[10- 14 C], synthesized according to this route. (author)

NCI calculations for understanding a physical phase transition in (C6H14N2)[Mn(H2O)6](SeO4)2

Science.gov (United States)

Naïli, Houcine; François, Michel; Norquist, Alexander J.; Rekik, Walid

2017-12-01

An organically templated manganese selenate, (C6H14N2)[Mn(H2O)6](SeO4)2, has been synthesized by slow evaporation and crystallographically characterized. The title compound crystallizes at room temperature in the monoclinic centrosymmetric space group P21/n, with the following unit cell parameters: a = 7.2373(4) Å; b = 12.5600(7) Å; c = 10.1945(7) Å; β = 91.155(4)°, V = 926.50(10) Å3and Z = 2. Its crystal structure is built of manganese(II) cations coordinated by six water molecules in octahedral geometry, disordered dabcodiium cations and selenate anions, resulting in an extensive hydrogen-bonding network. Differential scanning calorimetry (DSC) measurement indicated that the precursor undergoes a reversible phase transition at about 216 and 218 K during the cooling and heating processes respectively. Below this temperature the title compound is noncentrosymmetric with space group P21 and lattice parameters a = 7.2033(8) Å; b = 12.4981(13) Å; c = 10.0888(11) Å; β = 91.281(2)°, V = 908.04(17) Å3 and Z = 2. The disorder-order transformation of the C atoms of (C6H14N2)2+ cation may drive the structural phase transition. The low temperature phase obtained by breaking symmetry presents a fully ordered structure. The noncovalent interaction (NCI) method was used not only to locate, quantify, and visualize intermolecular interactions in the high and low temperature phases but also to confirm the phase transition detected by DSC measurement. The thermal decomposition of this new compound proceeds through four stages giving rise to the manganese oxide as final product at 850 °C.

Segregation effects and phase developments during solidification of alloy 625

DEFF Research Database (Denmark)

Højerslev, Christian; Tiedje, Niels Skat; Hald, John

2006-01-01

contained gamma-phase, Laves phase and, if carbon was dissolved in the liquid, niobium rich carbides formed. Molybdenum and niobium showed strong tendencies to segregate. Their segregation was balanced by inverse segregation of nickel and iron. The chromium concentration remained almost constant in gamma...

Synthesis of [21-14C]-fusarin C by enzymic demethylation and remethylation with [14C]-diazomethane

International Nuclear Information System (INIS)

Lu, S.-J.; Li, M.H.

1989-01-01

Fusarin C, a potent mutagen isolated from Fusarium moniliforme culture extracts, has been prepared radiolabeled in two steps by enzymic hydrolysis of the 21-methyl ester group, using phenobarbital induced microsomal preparations, followed by remethylation using [ 14 F]-diazomethane. Yields, based upon fusarin C, were essentially quantitative and approximately 10% of the [ 14 C]-methyl-nitrosourea, converted to diazomethane, reacted to yield [ 14 C]-fusarin C. (author)

Influence of annealing on structure and magnetic properties of Laves phase HfFe2

International Nuclear Information System (INIS)

Belosevic-Cavor, J.; Cekic, B.; Novakovic, N.; Ivanovic, N.; Manasijevic, M.

2004-01-01

Hyperfine fields (HFF) in a polycrystalline HfFe 2 binary compound were measured at 181 Ta probe ion sites using the time differential perturbed angular correlation (TDPAC) method. Analysis of TDPAC spectra obtained in measurements revealed two components. One of them corresponded to the magnetic perturbation with the value B hf1 (Ta) = 13.82(7) T at room temperature and it was ascribed to the interaction at the regular position of Hf in the cubic C15 (MgCu 2 -type) structure of the HfFe 2 compound. The second component with hyperfine field value of B hf2 (Ta) = 8.0(2) T is probably due to the presence of a minor amount of the hexagonal C14 (MgZn 2 -type) structure. Measurements showed that it had come to a change in the ratio of different components of TDPAC spectra with annealing, but the values for hyperfine fields for both components have not changed significantly. The origin of the hyperfine magnetic field and its difference in the two structures (C14 and C15) were discussed taking into account crystal structure effects. (orig.)

Extraction residue analysis on F82H-BA07 heat and other reduced activation ferritic/martensitic steels

International Nuclear Information System (INIS)

Nagasaka, Takuya; Hishinuma, Yoshimitsu; Muroga, Takeo; Li, Yanfen; Watanabe, Hideo; Tanigawa, Hiroyasu; Sakasegawa, Hideo; Ando, Masami

2011-01-01

Extraction residue analysis was conducted on reduced activation ferritic/martensitic steels, such as F82H-BA07 heat, F82H-IEA heat, JLF-1 JOYO heat and CLAM steel. M 23 C 6 type precipitates, TaC precipitates and Fe 2 W Laves phase were identified in the present analyses. M 23 C 6 precipitates were coarsened in F82H-BA07 compared with the other steels at as-normalized and tempered (NT) condition. TaC precipitate formation was enhanced in JLF-1 and CLAM compared with F82H-BA07 and F82H-IEA at as-NT condition. Laves phase were detected in F82H-IEA after aging above 550 o C, where solid solution W was significantly decreased. F82H-IEA exhibited hardening after aging at 400 and 500 o C for 100 khr, whereas softening at 600 and 650 o C. This behavior is similar to JLF-1 and CLAM, and can be understood by precipitation of TaC and Laves phase.

Spin reorientation and magnetoelastic properties of ferromagnetic T b1 -xN dxC o2 systems with a morphotropic phase boundary

Science.gov (United States)

Murtaza, Adil; Yang, Sen; Chang, Tieyan; Ghani, Awais; Khan, Muhammad Tahir; Zhang, Rui; Zhou, Chao; Song, Xiaoping; Suchomel, Matthew; Ren, Yang

2018-03-01

The spin reorientation (SR) and magnetoelastic properties of pseudobinary ferromagnetic T b1 -xN dxC o2 (0 ≤x ≤1.0 ) systems involving a morphotropic phase boundary (MPB) were studied by high-resolution synchrotron x-ray diffraction (XRD), magnetization, and magnetostriction measurements. The easy magnetization direction of the Laves phase lies along the 〈111 〉 axis with x 0.65 below Curie temperature (TC). The temperature-dependent magnetization curves showed SR; this can be explained by a two-sublattice model. Based on the synchrotron (XRD) and magnetization measurements, the SR phase diagram for a MPB composition of T b0.35N d0.65C o2 was obtained. Contrary to previously reported ferromagnetic systems involving MPB, the MPB composition of T b0.35N d0.65C o2 exhibits a low saturation magnetization (MS), indicating a compensation of the Tb and Nd magnetic moments at MPB. The anisotropic magnetostriction (λS) first decreased until x =0.8 and then continuously increased in the negative direction with further increase of Nd concentration. The decrease in magnetostriction can be attributed to the decrease of spontaneous magnetostriction λ111 and increase of λ100 with opposite sign to λ111. This paper indicates an anomalous type of MPB in the ferromagnetic T b1 -xN dxC o2 system and provides an active way to design novel functional materials with exotic properties.

Uptake and distribution of 14C during and following exposure to [14C]methyl isocyanate

International Nuclear Information System (INIS)

Ferguson, J.S.; Kennedy, A.L.; Stock, M.F.; Brown, W.E.; Alarie, Y.

1988-01-01

Guinea pigs were exposed to [ 14 C]methyl isocyanate ( 14 CH 3 -NCO, 14 C MIC) for periods of 1 to 6 hr at concentrations of 0.5 to 15 ppm. Arterial blood samples taken during exposure revealed immediate and rapid uptake of 14 C. Clearance of 14 C was then gradual over a period of 3 days. Similarly 14 C was present in urine and bile immediately following exposure, and clearance paralleled that observed in blood. Guinea pigs fitted with a tracheal cannula and exposed while under anesthesia showed a reduced 14 C uptake in blood indicating that most of the 14 C MIC uptake in normal guinea pigs occurred from retention of this agent in the upper respiratory tract passages. In exposed guinea pigs 14 C was distributed to all examined tissues. In pregnant female mice similarly exposed to 14 C MIC, 14 C was observed in all tissues examined following exposure including the uterus, placenta, and fetus. While the form of 14 C distributed in blood and tissues has not yet been identified, these findings may help to explain the toxicity of MIC or MIC reaction products on organs other than the respiratory tract, as noted by several investigators

Analysis of {sup 14}CO{sub 2} trapped {sup 14}C Sorbent, and {sup 14}C and {sup 3}H Radioactivity Determination in Resins and Oils from Nuclear Power Plants Using a Combustion Method

Energy Technology Data Exchange (ETDEWEB)

Ko, Young Gun; Kim, Chang Jong; Choi, Geun Sik; Chung, Kun Ho; Kang, Mun Ja [KAERI, Daejeon (Korea, Republic of)

2016-05-15

Tritium ({sup 3}H, T) generated in the heavy water and C fourteen ({sup 14}C) originated from the graphite moderator or structural materials of the nuclear power plant can cause acute and/or chronic harmful effects by inhalation and ingestion of these radionuclides owing to their binding affinity toward biomolecules and gas phase. {sup 3}H and {sup 14}C radioactivity in ion exchange resins and oils from nuclear power plants were determined by an oxidation (combustion) method. The 0.1 M HNO{sub 3} solution and the {sup 14}C sorbent trapped the {sub 3}H and {sup 14}C respectively in the gas from the combustion of samples. All samples were burned without ash in the combustion system. The reaction of CO{sub 2} and {sup 14}C sorbent was investigated by FT-IR analysis. The study demonstrated the different reaction mechanism according to the CO{sub 2} concentration. In the FT-IR study, it is clearly confirmed that CO{sub 2} from the burned 1 g of sample can be trapped in the {sup 14}C sorbent completely. During the reaction of CO{sub 2} and {sup 14}C sorbent, the temperature and the viscosity of {sup 14}C sorbent increased due to the decrease of enthalpy change and the bonding between each molecules of the sorbent. We expect that our FT-IR study could motivate the development of {sup 14}C sorbent and confirm the {sup 14}C trapping performance of the {sup 14}C sorbent.

Synthesis of [2-13C, 2-14C] 2-aminoethanol, [1-13C, 1-14C] 2-chloroethylamine, N,N'-bis([1-13C, 1-14C] 2-chloroethyl)-N-nitrosourea(BCNU) and N-([1-13C, 1-14C] 2-chloroethyl)-N-nitrosourea(CNU)

International Nuclear Information System (INIS)

Narayan, R.; Chang, C-j.

1982-01-01

[2- 13 C, 2- 14 C]2-Aminoethanol hydrochloride was prepared in good yield from Na*CN in a two step sequence by first converting the Na*CN to OHCH 2 *CN and then reducing the nitrile directly with a solution of borane-tetrahydrofuran complex. The reaction procedure was simple and the pure product could be obtained readily. Using this specifically labelled precursor, the synthesis of [1- 13 C, 1- 14 C]2-chloroethylamine hydrochloride, N-([1- 13 C, 1- 14 C]2-chloroethyl)-N-nitrosourea(CNU) and N,N'-bis([1- 13 C, 1- 14 C]2-chloroethyl)-N-nitrosourea(BCNU) in good yield without isotope scrambling was also reported. (author)

The Effect of Boron and Zirconium on the Structure and Tensile Properties of the Cast Nickel-Based Superalloy ATI 718Plus

Science.gov (United States)

Hosseini, Seyed Ali; Abbasi, Seyed Mehdi; Madar, Karim Zangeneh

2018-04-01

The effects of boron and zirconium on cast structure, hardness, and tensile properties of the nickel-based superalloy 718Plus were investigated. For this purpose, five alloys with different contents of boron and zirconium were cast via vacuum induction melting and then purified via vacuum arc remelting. Microstructural analysis by light-optical microscope and scanning electron microscope equipped with energy-dispersive x-ray spectroscopy and phase studies by x-ray diffraction analysis were performed. The results showed that boron and zirconium tend to significantly reduce dendritic arm spacing and increase the amount of Laves, Laves/gamma eutectic, and carbide phases. It was also found that boron led to the formation of B4C and (Cr, Fe, Mo, Ni, Ti)3B2 phases and zirconium led to the formation of intermetallic phases and ZrC carbide. In the presence of boron and zirconium, the hardness and its difference between dendritic branches and inter-dendritic spaces increased by concentrating such phases as Laves in the inter-dendritic spaces. These elements had a negative effect on tensile properties of the alloy, including ductility and strength, mainly because of the increase in the Laves phase. It should be noted that the largest degradation of the tensile properties occurred in the alloys containing the maximum amount of zirconium.

Structural and electrical phase transitions in the [(C2H5)4N]2ZnI3.86Cl0.14 system

Science.gov (United States)

Rhouma, Najla Mahbouli; Rayes, Ali; Mezzadri, Francesco; Delmonte, Davide; Cabassi, Riccardo; Calestani, Gianluca; Loukil, Mohamed

2017-12-01

The organic-inorganic hybrid non-centrosymmetric material [(C2H5)4N]2ZnI3.86Cl0.14 has been studied by X-ray diffraction (XRD), differential scanning calorimetry (DSC), dielectric and transport measurements. In analogy with the corresponding tetraiodo-zincate analogue, the material crystallizes at room temperature in the tetragonal system, space group P 4 ̅ 21m (No. 113), with lattice parameters a = 13.743(6) and c = 14.785(10) Å. DSC and XRD characterizations pointed out the occurrence of two phases transitions, one of second order at about 290 K and the other of the first order at T = 451 K. The former is related to an electrical transition from insulating to thermally activated transport mechanism displaying clear hints of ionic conduction, the latter leads to a phase showing the typical features of plastic crystals in its powder XRD pattern. The pattern was indexed by an orthorhombic cell, a = 15.724(1), b = 17.907(1) and c = 10.585(1) Å, and a reliable model was found and refined in the Pna21 space group. The model consists of ordered tetrahedral ZnCl42- units intercalated by fully disordered tetraethylammonium cations.

Double labeling autoradiography. Cell kinetic studies with 3H- and 14C-thymidine

International Nuclear Information System (INIS)

Schultze, B.

1981-01-01

Examples of the multiple applicability of the double labeling method with 3 H- and 14 C-TdR are demonstrated. Double labeling with 3 H- and 14 C-TdR makes it possible to determine the cycle and its phases with high precision by modifying the usual percent labeled mitoses method with a single injection of 3 H-TdR. In addition, data is provided on the variances of the transit times through the cycle phases. For example, in the case of the jejunal crypt cells of the mouse, the transit times through successive cycle phases are uncorrelated. In the case of glial cells the double labeling method provides cell kinetic parameters despite the paucity of proliferating glial cells. In the adult untreated animal, glial cell mitoses are so rare that the percent labeled mitoses method can not be utilized. However, the S-phase duration can be measured by double labeling and the cycle time can be determined by the so-called method of labeled S phases. With the latter method the passage through the S phase of the 3 H-TdR-labeled S phase cells can be registered by injecting 14 C-TdR at different time intervals following 3 H-TdR application. In this way an S-phase duration of about 10 hr and a cycle time of about 20 hr was found for glial cells in the adult untreated mouse. An exchange of glial cells between the growth fraction and the nongrowth fraction has also been shown by double labeling. A quite different application of the double labeling method with 3H- and 14 C-TdR is the in vivo study of the cell cycle phase-specific effect of drugs used in chemotherapy of tumors. The effect of vincristine on these cells has been studied. Vincristine affects cells in S and G2 in such a manner that they are arrested during the next metaphase and subsequently become necrotic. It has no effect on G1 cells

Myo-inositol-14C, phytic acid-14C and ferric phytate-14C metabolism through microbian action in an andosol soil

International Nuclear Information System (INIS)

Gonzalez I, J.

1977-01-01

The myo-inositol- 14 C, phytic acid- 14 C and ferric phytate- 14 C compounds were incubated in an andosol soil at 70% of the field capacity and at 36.5 deg C during twelve days. These compounds suffered a microbian oxidation at 14 CO 2 of 61.0, 1.9 and 0% respectively. The fixation of the phytic acid- 14 C was observed through the fast decrease in the metabolism, due to the formation of complexes with the Fe and Al (phytates). The myo-inositol- 14 C metabolism was reduced by a factor of nine at the second incubation day. The following mechanisms were observed in the myo-inositol metabolism: (i) adsorption of the inositol by the soil minerals, (ii) adsorption by humic acids, (iii) myo-inositol phosphorylation and (iv) epimerization of myo-inositol to chiro-inositol. It was found that the (i) and (ii) formation depends on the soil microbian activity. The (i), (ii) and (iii) interactions were considered as possible mechanisms for the inhibition of the myo-inositol microbian oxidation. The inhibition of the myo-inositol oxidation through adsorption or phosphorylation is considered as a chemical blockade for the hydroaxial group, avoiding this way a microbian oxidation stereospecific of this hydroxil group. (author)

Creep and precipitation behaviors of AL6XN austenitic steel at elevated temperatures

Science.gov (United States)

Meng, L. J.; Sun, J.; Xing, H.

2012-08-01

Creep behaviors of the solution-treated AL6XN austenitic stainless steel have been investigated at 873-1023 K and 120-260 MPa. The results showed that the creep stress exponent and activation energy of the AL6XN steel are 5 and 395.4 kJ/mol, respectively in the power-law breakdown regime. TEM observations revealed that dislocations distributed homogenously in grains. The creep deformation mechanism is mainly attributed to viscous dislocation glide. Precipitates in the steel after creep deformation were additionally analyzed by TEM, and the results showed that there are four different types of precipitates, such as M23C6, M6C, σ phase and Laves phase. The M23C6 carbides were observed at grain boundaries in the steel after creep at 873 K. The M6C, σ phase and Laves phase precipitates were found when the creep temperature increases to 923-1023 K. Although the AL6XN steel exhibited low steady state creep rates, a high volume fraction of brittle precipitates of σ and Laves phases reduced the creep lifetime of the steel at elevated temperatures.

Creep and precipitation behaviors of AL6XN austenitic steel at elevated temperatures

Energy Technology Data Exchange (ETDEWEB)

Meng, L.J. [School of Materials Science and Engineering, Shanghai Jiaotong University, Dongchuan Road 800, Shanghai 200240 (China); Sun, J., E-mail: jsun@sjtu.edu.cn [School of Materials Science and Engineering, Shanghai Jiaotong University, Dongchuan Road 800, Shanghai 200240 (China); Xing, H. [School of Materials Science and Engineering, Shanghai Jiaotong University, Dongchuan Road 800, Shanghai 200240 (China)

2012-08-15

Creep behaviors of the solution-treated AL6XN austenitic stainless steel have been investigated at 873-1023 K and 120-260 MPa. The results showed that the creep stress exponent and activation energy of the AL6XN steel are 5 and 395.4 kJ/mol, respectively in the power-law breakdown regime. TEM observations revealed that dislocations distributed homogenously in grains. The creep deformation mechanism is mainly attributed to viscous dislocation glide. Precipitates in the steel after creep deformation were additionally analyzed by TEM, and the results showed that there are four different types of precipitates, such as M{sub 23}C{sub 6}, M{sub 6}C, {sigma} phase and Laves phase. The M{sub 23}C{sub 6} carbides were observed at grain boundaries in the steel after creep at 873 K. The M{sub 6}C, {sigma} phase and Laves phase precipitates were found when the creep temperature increases to 923-1023 K. Although the AL6XN steel exhibited low steady state creep rates, a high volume fraction of brittle precipitates of {sigma} and Laves phases reduced the creep lifetime of the steel at elevated temperatures.

Phase Transformation in Cast Superaustenitic Stainless Steels

Energy Technology Data Exchange (ETDEWEB)

Lee Phillips, Nathaniel Steven [Iowa State Univ., Ames, IA (United States)

2006-01-01

Superaustenitic stainless steels constitute a group of Fe-based alloys that are compositionally balanced to have a purely austenitic matrix and exhibit favorable pitting and crevice corrosion resistant properties and mechanical strength. However, intermetallic precipitates such as sigma and Laves can form during casting or exposure to high-temperature processing, which degrade the corrosion and mechanical properties of the material. The goal of this study was to accurately characterize the solid-solid phase transformations seen in cast superaustenitic stainless steels. Heat treatments were performed to understand the time and temperature ranges for intermetallic phase formations in alloys CN3MN and CK3MCuN. Microstructures were characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy and wavelength dispersive spectroscopy (EDS, WDS). The equilibrium microstructures, composed primarily of sigma and Laves within purely austenitic matrices, showed slow transformation kinetics. Factors that determine the extent of transformation, including diffusion, nucleation, and growth, are discussed.

Mechanisms of improving the cyclic stability of V-Ti-based hydrogen storage electrode alloys

International Nuclear Information System (INIS)

Miao He; Wang Weiguo

2010-01-01

Research highlights: → The corrosion resistance of V-based phase is much lower than that of C14 Laves phase of V-Ti-based alloys. → The addition of Cr which mostly distributes in V-based phase can effectively increase the anti-corrosion ability of V-Ti-based alloys. → The addition of Cr which mostly distributes in V-based phase can effectively increase the anti-corrosion ability of V-Ti-based alloys. - Abstract: In this work, the mechanisms of improving the cyclic stability of V-Ti-based hydrogen storage electrode alloys were investigated systemically. Several key factors for example corrosion resistance, pulverization resistance and oxidation resistance were evaluated individually. The V-based solid solution phase has much lower anti-corrosion ability than C14 Laves phase in KOH solution, and the addition of Cr in V-Ti-based alloys can suppress the dissolution of the main hydrogen absorption elements of the V-based phase in the alkaline solution. During the charge/discharge cycling, the alloy particles crack or break into several pieces, which accelerates their corrosion/oxidation and increases the contact resistance of the alloy electrodes. Proper decreasing the Vickers hardness and enhancing the fracture toughness can increase the pulverization resistance of the alloy particles. The oxidation layer thickness on the alloy particle surface obviously increases during charge/discharge cycling. This deteriorates their electro-catalyst activation to the electrochemical reaction, and leads to a quick degradation. Therefore, enhancing the oxide resistance can obviously improve the cyclic stability of V-Ti-based hydrogen storage electrode alloys.

A procedure for batch separation of 14C-hexose from 14C-sucrose

International Nuclear Information System (INIS)

Tarpley, L.; Vietor, D.M.

1991-01-01

This presentation describes a method for separating 14 C-hexose from 14 C-sucrose in extracts of plant tissue. Portions of ethanol extracts are treated with activated charcoal in microcentrifuge tubes. Aliquots are removed, ethanol evaporated and replaced with reaction mixture that phosphorylates hexose (HEPPS, K 2 HPO 4 , Mg(C 2 H 3 O 2 ) 2 , ovalbumen, Na 2 ATP, yeast hexokinase). After a time course, the hexokinase reaction is stopped (slowed considerably) to minimize effects of contamination enzyme activities. The stopping agent used is lyxose, a nonphosphorylable analogue of glucose. The strong anionic charge of phosphate introduced through the hexokinase action results in binding (> 95%) of hexose-phosphate to anion-exchange resin. Sucrose remains unbound (> 95%) in solution. This batch ion-exchange is performed in microcentrifuge tubes to allow many samples to be processed simultaneously. Recovery of radiolabel in extracts is complete (99%), and determinations are repeatable (cv = 23%). This method for routinely separating and quantifying 14 C-hexose and 14 C-sucrose in plant tissue extracts can contribute to the economy and feasibility of studies of 14 C-photoassimilate partitioning to soluble sugars within and among plant tissues

Syntheses of (6- sup 14 C) and (5-carboxy, 6- sup 14 C sub 2 )nitrendipine

Energy Technology Data Exchange (ETDEWEB)

Maul, N.; Scherling, D. (Bayer AG, Wuppertal (Germany, F.R.). Inst. fuer Pharmakologie)

1989-04-01

(6-{sup 14}C)Nitrendipine synthesis started from barium({sup 14})carbonate, which was converted to (1-{sup 14}C)acetyl chloride. The acid chloride was condensed with Meldrum's acid (2,2-dimethyl-1,3-dioxane-4,6-dione). The resulting intermediate was treated with boiling methanol to give methyl (3-{sup 14}C)acetoacetate. The reaction with gaseous ammonia in toluene yielded the corresponding methyl 3-amino(3-{sup 14}C)crotonate which was condensed with ethyl 2-(3-nitro-benzylidene) acetoacetate to obtain (6-{sup 14}C)nitrendipine. (author).

Characterization of laves phases in the pseudobinary Zr Cr2-Zr Fe2 system by Moessbauer spectroscopy

International Nuclear Information System (INIS)

Kanter, F.L. de; Badler, C.S.; Granovski, M.; Arias, D.

1988-01-01

57 Fe Moessbauer spectroscopy together with XRD and optical metallography were used to verify the two phase boundaries of the ZrCr 2 -ZrFe 2 pseudobinary phase diagram. Samples with adequate ternary and binary composition, treated at 1450 0 C, were studied. Experimental results indicate that in some cases the two phase boundaries should be modified. (author)

Initial study on Z-phase strengthened 9-12% Cr steels by atom probe tomography

Energy Technology Data Exchange (ETDEWEB)

Liu, Fang; Andren, Hans-Olof [Chalmers Univ. of Technology, Goeteborg (Sweden). Dept. of Applied Physics

2010-07-01

The microstructure of two different types of Z-phase strengthened experimental steels, CrNbN-based or CrTaN-based, was investigated. Both steels underwent aging at 650 C for relatively short period of time, 24 hours or 1005 hours. Atom probe tomography was used to study the chemical composition of the matrix and precipitates, and the size and number density of the small precipitates. Both steels contain Laves phase at prior austenite grain boundaries and martensitic lath boundaries. The CrTaN-based steel was found more promising due to its finer and more densely distributed precipitates after 1005 hour aging. (orig.)

Experimental Investigation and Analytical Prediction of σ-Phase Precipitation in AISI 316L Austenitic Stainless Steel

Science.gov (United States)

Sahlaoui, Habib; Sidhom, Habib

2013-07-01

The phase precipitation in industrial AISI 316L stainless steel during aging for up to 80,000 hours between 823 K and 1073 K (550 °C and 800 °C) has been studied using transmission electron microscopy, scanning transmission electron microscopy, and carbon replica energy-dispersive X-ray microanalysis. Three phases were identified: Chromium carbides (M23C6), Laves phase ( η), and σ-phase (Fe-Cr). M23C6 carbide precipitation occurred firstly and was followed by the η and σ-phases at grain boundaries when the aging temperature is higher than 873 K (600 °C). Precipitation and growth of M23C6 create chromium depletion zones at the grain boundaries and also retard the σ-phase formation. Thus, the σ-phase is controlled by the kinetic of chromium bulk diffusion and can appear only when the chromium reaches, at grain boundaries and at the M23C6/ γ and M23C6/ η/ γ interfaces, content higher than a critical value obtained by self-healing. An analytical model, based on equivalent chromium content, has been established in this study and successfully validated to predict the time-temperature-precipitation diagram of the σ-phase. The obtained diagram is in good agreement with the experimental results.

14C2H4: distribution of 14C-labeled tissue metabolites in pea seedlings

International Nuclear Information System (INIS)

Giaquinta, R.; Beyer, E. Jr.

1977-01-01

The 14 C-metabolite distribution pattern following 14 C 2 H 4 metabolism in intact pea seedlings (Pisum sativum L.) was determined under various conditions. After a 24 hr exposure to 14 C 2 H 4 , the majority of 14 C-metabolites were water-soluble (60-70%) with lesser amounts in the protein (10-15%), lipid (1%), and insoluble (1-2%) fractions. Ion exchange chromatography of the water-soluble components into basic, neutral, and acidic fractions revealed a 50:40:10 distribution, respectively. Chromatography of the neutral fraction revealed two regions of radioactivity (Rf=0.38) and 0.63 which did not cochromatograph with twenty-two known sugars or neutral metabolites. Chromatograms of the basic fraction contained 3 regions of radioactivity. Similar distribution patterns were noted when 14 C 2 H 4 exposure was followed by a 6 hr air chase or when 5% CO 2 , an antagonist of ethylene action, was present during the exposure. Marked differences in the 14 C-metabolite distribution patterns were obtained when 14 CO 2 was substituted for 14 C 2 H 4 . These results indicate that the metabolic pathway involved in ethylene metabolism is different from that involved in intermediately carbon metabolism. (auth.)

The Zr-Ti-Cr system. Equilibria at 900 and 1100 C degrees

International Nuclear Information System (INIS)

Arico, Sergio F.; Gribaudo, Luis M.

2003-01-01

Main contributions to the knowledge of the ternary system Zr-Ti-Cr were published in the sixties. Stability domains of phases at temperatures between 500 and 1400 C degrees were there presented. Here, results related to the phase diagram at 900 and 1100 C degrees are informed. Three alloys with 40 at.% Cr and different Zr/Ti ratios and one more, richer in Cr, were elaborated. Specimens of the alloys were heat treated 1000 and 800 h at 900 and 1100 C degrees respectively. Phase characterizations were performed by optic metallography and X-ray diffraction analysis. Compositions were determined by microprobe. Alloys with 40 at.% Cr at both temperatures have biphasic equilibria between the intermetallic Laves phase AB 2 and the body-centered cubic solid solution containing principally zirconium and titanium. The Cr-rich alloy presents equilibrium of the AB 2 compound and the Cr-rich solid solution. Results of the present and previous works are used in order to propose new isothermal sections at 900 and 1100 C degrees. (author)

Synthesis of 14C analogue of 1,2-diaryl-[2-14C]-pyrroles

International Nuclear Information System (INIS)

Saemian, N.; Shirvani, G.; Matloubi, H.

2007-01-01

Three 1,2-diaryl pyrroles selective COX-2 inhibitors, 2-(4-fluorophenyl)-5-methyl-1-(4-methylsulfonyl-phenyl)-1H pyrrole, 2-(4-fluorophenyl)-1- [4-(methylsulfonyl) phenyl]-1H-pyrrole and 4-[2-(4-fluorophenyl)-1H-pyrrol-1-yl]benzenesulfon-amide, all three labeled with 14 C in the 2-position were prepared from para-fluoro-benzaldehyde-[carbonyl- 14 C]. (author)

Coarsening of (Fe, Cr)23C6 carbide phase on the tempering of 14Kh17N2 chromium-nickel steel

International Nuclear Information System (INIS)

Psarev, V.I.

2002-01-01

Paper lists the results of computer analysis of distribution according to sizes (Fe, Cr) 23 C 6 microparticles resulting from 14Kh17N2 steel tempering under 700 Deg C. Data were obtained at the maximum beneficial magnification of a light microscope. The mentioned curves of distribution densities are characterized by more reliable run from most permissible sizes of dispersed particles. Application of general rules of distributions and of previously elaborated procedure to identify experimental histograms with theoretical distributions enables to derive valuable information on dynamics of coarsening of a disperse phase in this case, as well [ru

Turnover of 14C-glucose in soils and its relationship with soil characters

International Nuclear Information System (INIS)

Ni Jinzhi; Xu Jianmin; Xie Zhengmiao; Ye Qingfu

2001-01-01

The turnover of 14 C-glucose added in 13 soils was studied. The turnover rate of 14 C-glucose can be divided into three phases: 0 - 3d, 3 - 28d and 28 - 294d. The range of the turnover rate and half -life of 14 C-glucose were 1.3 x 10 -1 - 2.5 x 10 -1 d -1 and 3 - 5d, 0.7x 10 -2 - 1.2 x 10 -2 d -1 and 58 - 97d, 0.5 x 10 -3 - 1.4 x 10 -3 d -1 and 491 - 1504d, respectively. Correlation analysis showed that from 0 to 3 days the turnover rate of 14 C-glucose had significant positive correlation with soil qCO 2 , from 3 to 28 days, the turnover rate of 14 C-glucose had no significant correlation with soil physico-chemical and biological properties. The turnover rate of 14 C-glucose had significant or highly significant negative correlation with soil total organic carbon, total nitrogen, CEC and significant positive correlation with soil sand content during the period from 28 to 294 days. Turnover of 14 C-glucose during the third period has close correlation with soil properties

Synthesis of pinacolyl [14C]methylphosphonochloridate

International Nuclear Information System (INIS)

Horvat, J.; Keglevic, D.; Klaic, B.; Kveder, S.; Ladesic, B.; Cosic, M.; Zupanc, S.

1982-01-01

A three-step synthetic route to pinacolyl [ 14 C]methylphosphonochloridate (3) from [ 14 C]methyl iodide is described. Condensation of sodium di-n-butyl phosphite with [ 14 C]methyl iodide gave di-n-butyl [ 14 C]methylphosphonate (1) which was converted into [ 14 C]methylphosphonic dichloride (2) by prolonged refluxing with thionyl chloride. Reaction of 2 with pinacolyl alcohol in the presence of N,N-di-n--propylaniline as the base afforded the title compound 3. The radiochemical yield of redistilled 3 was 34,2% based on 1, and the overall radiochemical yield was 20,0% from [ 14 C]methyl iodide. (author)

Preparation of D-[U-14C]galactose and α-D-[U-14C]galactose-1-phosphate

International Nuclear Information System (INIS)

Kolina, J.; Hromadkova, B.

1989-01-01

Optically pure D-[U- 14 C]galactose was prepared on a preparatory scale using the galactokinase enzyme. The suggested procedure allows to also prepare a α-D-[U- 14 C]galactose-1-phosphate and L-[U- 14 ]galactose giving good yield. The experiments proved that the raw fraction isolated from yeast of the Kluyveromyces fragilis strain or the Kluyveromyces lactis strain shows sufficient activity. Phosphorylation of D-[U- 14 C]galactose practically terminates after 30 mins of incubation. DL-[U- 14 C]galactose isolated using preparatory paper chromatography from the acid hydrolyzate of [U- 14 C] polysaccharide is a satisfactory radioactive precursor. The developed preparation procedure theoretically contributed towards the further elucidation of the problem of the proportional representation of galactose stereo-isomers in extracellular polysaccharide isolated from red algae. In this respect data in the literature differ and some sources state a significantly higher propertion of L-galactose. The experiments showed that [U- 14 C] polysaccharide isolated from the red algae Porphyridium cruentum prevalently contains D-[U- 14 C]galactose, which confirms the process of enzyme reaction. (author). 1 tab., 4 refs

Root-uptake of 14C derived from acetic acid and 14C transfer to rice edible parts

International Nuclear Information System (INIS)

Ogiyama, Shinichi; Suzuki, Hiroyuki; Inubushi, Kazuyuki; Takeda, Hiroshi; Uchida, Shigeo

2010-01-01

Three types of culture experiments using paddy rice (Oryza sativa L.) were performed to examine root-uptake of 14 C in the form of acetic acid: double pot experiment (hydroponics), wet culture experiment (submerged sand medium), and chamber experiment (hydroponics and submerged sand medium). The 14 C radioactivity in the plant, mediums, and atmospheric carbon dioxide ( 14 CO 2 ) in the chamber were determined, and the distribution of 14 C in the plant was visualized using autoradiography. In the double pot experiment, the shoot of the plant and the lower root which was soaked in the culture solution had 14 C radioactivity, but the upper root which did not have contact with the solution had none. There were also 14 C radioactivity in the grains and roots in the wet culture experiment. Results of the chamber experiment showed that 14 CO 2 gas was released from the culture solution in both types of cultures. Results indicated that the 14 C-acetic acid absorbed by rice plant through its root would be very small. Most of the 14 C-acetic acid was transformed into gaseous forms either in the culture solution or rhizosphere. A relatively longer time would be needed to assimilate 14 C derived from acetic acid to grain parts after it was once absorbed by the shoot through the root. Availability of 14 C for the plant in sand culture was considered to be decreased compared with that for the plant in the hydroponics experiment. It was suggested that rice plant absorbed and assimilated 14 C through the plant roots not because of uptake of 14 C-acetic acid but because of uptake of 14 C in gaseous forms such as 14 CO 2 .

Phase Evolution in and Creep Properties of Nb-Rich Nb-Si-Cr Eutectics

Science.gov (United States)

Gang, Florian; Kauffmann, Alexander; Heilmaier, Martin

2018-03-01

In this work, the Nb-rich ternary eutectic in the Nb-Si-Cr system has been experimentally determined to be Nb-10.9Si-28.4Cr (in at. pct). The eutectic is composed of three main phases: Nb solid solution (Nbss), β-Cr2Nb, and Nb9(Si,Cr)5. The ternary eutectic microstructure remains stable for several hundred hours at a temperature up to 1473 K (1200 °C). At 1573 K (1300 °C) and above, the silicide phase Nb9(Si,Cr)5 decomposes into α-Nb5Si3, Nbss, and β-Cr2Nb. Under creep conditions at 1473 K (1200 °C), the alloy deforms by dislocation creep while the major creep resistance is provided by the silicide matrix. If the silicide phase is fragmented and, thus, its matrix character is destroyed by prior heat treatment [ e.g., at 1773 K (1500 °C) for 100 hours], creep is mainly controlled by the Laves phase β-Cr2Nb, resulting in increased minimum strain rates. Compared to state of the art Ni-based superalloys, the creep resistance of this three-phase eutectic alloy is significantly higher.

Deformation-induced phase transformation in 4H–SiC nanopillars

International Nuclear Information System (INIS)

Chen, Bin; Wang, Jun; Zhu, Yiwei; Liao, Xiaozhou; Lu, Chunsheng; Mai, Yiu-Wing; Ringer, Simon P.; Ke, Fujiu; Shen, Yaogen

2014-01-01

The deformation behaviour of single-crystal SiC nanopillars was studied by a combination of in situ deformation transmission electron microscopy and molecular dynamics simulations. An unexpected deformation-induced phase transformation from the 4H hexagonal structure to the 3C face-centred cubic structure was observed in these nanopillars at room temperature. Atomistic simulations revealed that the 4H to 3C phase transformation follows a stick–slip process with initiation and end stresses of 12.1–14.0 and 7.9–9.0 GPa, respectively. The experimentally measured stress of 9–10 GPa for the phase transformation falls within the range of these theoretical upper and lower stresses. The reasons for the phase transformation are discussed. The finding sheds light on the understanding of phase transformation in polytypic materials at low temperature

Preparation of arginine (guanide 14C)

International Nuclear Information System (INIS)

Pichat, L.; Baret, C.

1960-01-01

Reaction of anhydrous ammoniac at 800 deg. C on 14 CO 3 Ba gives rise to barium cyanamide 14 C with a yield of about 98 per cent. Addition on H 2 S on cyanamide 14 C leads to thiourea 14 C with a 85 per cent yield, which is quantitatively transformed into S-ethyl-isothiouronium iodide by treatment with methyl iodide. This 14 C-isothiouronium salt is used to introduce 14 C guanide group in α-N-tosyl-ornithine; tosyl group in α-N-tosyl-arginine thus obtained is then removed by hydrolysis with hydrochloric acid. Arginine is separated as flavianic acid salt and is purified on exchange resin Dowex-50. The overall yield based on 14 CO 3 Ba is 25 per cent. (author) [fr

Synthesis of disodium [benzene-U-{sup 14}C]-(4-chlorophenylthio)methylenediphosphonate, [benzene-U-{sup 14}C]-tiludronate

Energy Technology Data Exchange (ETDEWEB)

Burgos, Alain; Ellames, G.J. [Alnwick Research Centre (United Kingdom). Dept. of Metabolism and Pharmacokinetics

1995-12-31

Disodium [benzene-U-{sup 14}C]-(4-chlorophenylithio)methylenediphosphonate, [benzene-{sup 14}C]-Tiludronate, 2, has been prepared in six steps from [benzene-U-{sup 14}C]-acetanilide in an overall radiochemical yield of 41%. A key step in this transformation was the efficient conversion of [U-{sup 14}C]-4-chloroaniline to [benzene-U-{sup 14}C]-4-chlorophenylthiocyanate, 5, in 83% yield by treatment of the corresponding diazonium salt, 9 with iron(111) thiocyanate. It should be noted that formation of the isomeric [benzene-U-{sup 14}C]-4-chlorophenylisothiocyanate, 11, as a byproduct, was observed in only {approx} 1% yield. (author).

Synthesis of cholesterol 26. C{sup 14} (1961); Synthese du cholesterol {sup 14}C-26 (1961)

Energy Technology Data Exchange (ETDEWEB)

Herbert, M; Pichat, L [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1961-07-01

Cholesterol 26 {sup 14}C is synthesized from methylmagnesium iodide {sup 14}C with a 48 per cent overall yield. Cholesterol is purified by chromatography on alumina. The various intermediates of the synthesis are characterized by thin-layer chromatography according to Stahl. (authors) [French] Le cholesterol {sup 14}C-26 est synthetise a partir d'iodure de methyl magnesium {sup 14}C, avec un rendement de 48 pour cent par rapport a l'iodure de methyl {sup 14}C mis en jeu. Le cholesterol est purifie par chromatographie sur alumine. Les intermediaires de la synthese sont caracterises par chromatographie en couche mince, selon Stahl. (auteurs)

Synthesis of [methyl-14C]crotonobetaine from DL-[methyl-14C]carnitine

International Nuclear Information System (INIS)

Loester, H.; Seim, H.

1996-01-01

The causes of carnitine deficiency syndromes are not completely understood, but decomposition of L-carnitine in vivo is likely to be involved. Carnitine is metabolized to γ-butyrobetaine, and crotonobetaine is probably an intermediate in this pathway. To validate experimentally the precursor-product relationship between the three physiologically occuring γ-betaines - L-carnitine, crotonobetaine, γ-butyrobetaine - labelling with stable or radioactive isotopes became necessary. Methyl-labelled carnitine isomers (L(-)-, D(+)- or DL-) or γ-butyrobetaine can be easily synthesized by methylation of 4-amino-3-hydroxybutyric acid isomers or 4-aminobutyric acid, respectively. Because of problems with the 4-aminocrotonic acid, we synthesized labelled crotonbetaine from labelled carnitine. Thus, DL-[methyl- 14 C]carnitine was dehydrated by reaction with concentrated sulfuric acid. After removal of the latter the products were separated and purified by ion exchange chromatography on DOWEX 50 WX8 (200 - 400 mesh) and gradient elution with hydrochloric acid. In addition to the labelled main product [methyl- 14 C]crotonobetaine (yield about 50 %), [methyl- 14 C]glycine betaine and [methyl- 14 C]acetonyl-trimethylammonium (ATMA) were formed. The end products were identified by combined thin layer chromatography/autoradiography and quantified by liquid scintillation counting. (Author)

Fe-15Ni-13Cr austenitic stainless steels for fission and fusion reactor applications. II. Effects of minor elements on precipitate phase stability during thermal aging

International Nuclear Information System (INIS)

Lee, E.H.; Mansur, L.K.

2000-01-01

The precipitate phase stability in Fe-15Ni-13Cr base austenitic alloys was investigated as a function of minor alloying additions after thermally aging at 600 deg. C and 675 deg. C for times ranging from 24 h to one year. Seven major precipitate phases were found in aged specimens, including M 23 C 6 , Laves, Eta (η), TiO, NbC, MC, and M 2 P. The types and amounts of precipitate phases varied with alloying element additions, aging temperature, and aging time. By analyzing the composition of each individual particle, it was possible to determine the essential constituent elements for each phase. From this information, a strategy to promote or suppress certain precipitate phases was developed. Among the seven phases, the most desirable precipitate phases were considered to be MC and M 2 P, because these particles form on a fine scale with a high number density and, therefore, can serve as effective gas atom trap sites under irradiation

Synthesis of 14C-dehydrocorydaline chloride

International Nuclear Information System (INIS)

Zhang Rui; Wang Ding

1988-01-01

A method for synthesis of 14 C-dehydrocorydaline chloride is described. In the presence of sodium hydroxide, acetonylpalmatine is reacted with 14 C-methyl iodide in sealed glass ampoule to give 14 C-13-methylpalmatine iodide which is then converted to chloride. The radiochemical purity of 14 C-dehydrocorydaline determined by TLC is over 98% and the labelling efficiency is 54%

Synthesis of [5,6-13C2, 1-14C]olivetolic acid, methyl [1'-13C]olivetolate and [5,6-13C2, 1-14C]cannabigerolic acid

International Nuclear Information System (INIS)

Porwoll, J.P.; Leete, E.

1985-01-01

Potential advanced intermediates in the biosynthesis of delta 9 -tetrahydrocannabinol, the major psychoactive principle of marijuana, have been synthesized labeled with two contiguous 13 C atoms and 14 C. Methyl [5,6- 13 C 2 , 1- 14 C]olivetolate was prepared from lithium [ 13 C 2 ]acetylide and dimethyl [2- 14 C]malonate. Reaction with geranyl bromide afforded methyl [5,6- 13 C 2 , 1- 14 C]cannabigerolate, and hydrolysis of these methyl esters with lithium propyl mercaptide yielded the corresponding labeled acids. The 13 C- 13 C couplings observable in the 13 C NMR spectra of these 13 C-enriched compounds and their synthetic precursors are recorded. Methyl [1'- 14 C]olivetolate was prepared from 13 CO 2 to confirm assignments of the 13 C chemical shifts in the pentyl side chain of these compounds. (author)

Vaporization, fusion and sublimation enthalpies of the dicarboxylic acids from C4 to C14 and C16

International Nuclear Information System (INIS)

Roux, Maria Victoria; Temprado, Manuel; Chickos, James S.

2005-01-01

The fusion enthalpies of the series butanedioic acid through to tetradecanedioic acid and hexadecanedioic acids have been measured by DSC. In addition to fusion, a number of solid-solid phase transitions have also been detected in these diacids. The vaporization enthalpies of these compounds have been measured by correlation gas chromatography using the vaporization enthalpies of butanedioic, hexanedioic and decanedioic acids as standards. The vaporization enthalpies of the diacids from C 4 to C 10 correlated linearly with the number of methylene groups present. Above C 10 , the vaporization enthalpies of C 11 -C 14 and C 16 begin to deviate from linearity. The vaporization enthalpies for these compounds are dependent on the temperature of the GC column used. Similar departure from linearity has also been observed previously in the sublimation enthalpies for these compounds. The results are discussed in terms of formation of a cyclic intramolecular hydrogen bonded network in the gas phase similar to the bimolecular association observed in smaller mono-carboxylic acids at ambient temperatures

Bepaling van 14C in afvalwater

NARCIS (Netherlands)

Hiemstra YS; Kwakman PJM; Nissan LN; Aldenkamp FJ; LSO

1998-01-01

In opdracht van de Hoofdinspectie Milieuhygiene van het ministerie van VROM heeft LSO een methode ontwikkeld om 14C in afvalwater van nucleaire installaties te bepalen. De methode meet organisch gebonden-14C en anorganisch-14C in de vorm van carbonaat (14CO32-) in afvalwater. Het rapport

Metabolism of [ 14 C]GA 19 and [ 14 C]GA 53 by ecotypes of Betula ...

African Journals Online (AJOL)

Continuing with this line of research, we studied the metabolism of 14C-labelled GA19 and GA53. [14C]GA19 and [14C] A53 were applied to the apices of the northern ecotype (67º N) and to the leaves of the southern ecotype (64º N) of Betula pendula Roth. under different photoperiods and at different times in order to ...

Effect of tolbutamide on 14C-sodium bicarbonate and 14C-alanine metabolism in isolated rat hepatocytes

International Nuclear Information System (INIS)

Kunjathoor, V.V.; Ye, Y.; Pillai, U.A.; Ferguson, P.W.; Medon, P.J.

1990-01-01

Tolbutamide (TOLB) is a sulfonylurea commonly used in the treatment of noninsulin-dependent diabetes mellitus. Studies have shown that TOLB affects gluconeogenesis and glycolysis from various substrates in the liver. Specifically, TOLB inhibits gluconeogenesis from lactate in a dose-dependent manner. In order to further clarify tolbutamide's mechanism of action, its effect on the incorporation of 14 C from NaH 14 CO 3 and 14 C-alanine into glucose, lactate or pyruvate in the presence of lactate was measured. Rat hepatocytes were incubated with lactate (2.0 mM) with or without TOLB (1.0 mM) in the presence of NaH 14 CO 3 or 14 C-alanine. TOLB inhibited the incorporation of C 14 from NaHCO 3 and alanine into glucose by 55 and 56%, respectively. TOLB did not alter the incorporation of C 14 from NaHCO 3 into lactate or pyruvate. TOLB did not affect the incorporation of 14 C from alanine into lactate but produced a pooling of 14 C as pyruvate. The authors data support studies demonstrating the TOLB produces its actions, in part, by increasing the concentration of fructose-2,6-bisphosphate and inhibiting pyruvate carboxylase

Sources of C-14 generation and associated doses; Fuentes de generacion de C-14 y dosis asociadas

Energy Technology Data Exchange (ETDEWEB)

Amado, Valeria A; Biaggio, Alfredo L; Canoba, Analia C; Curti, Adriana R. [Autoridad Regulatoria Nuclear, Buenos Aires (Argentina)], E-mail: vamado@cae.arn.gov.ar

2009-07-01

C-14 is a radioactive isotope of C with a half-life of 5700 years that decays to N-14 by emission of beta radiation. It is naturally produced in the upper atmosphere by cosmic ray neutrons via the (n;p) reaction over N-14. Anthropogenic C-14 has been generated in the past by atmospheric nuclear weapon tests and it is currently produced during the operation of nuclear reactors. Once released this radionuclide behaves in the biosphere as the standard carbon cycle. Since the beginning of the industrial period the relationship Carbon-14/Stable Carbon has changed continuously, and so the dose incurred by the world population. In this paper the main anthropogenic activities that modified such relationship are presented and analyzed: the Suess effect and the generation of nuclear energy. It is concluded that the current trend of reduction of the total dose due to C-14 will continue during the next decades. Finally it is indicated that in order to prevent an excessive accumulation of this radionuclide in the biosphere, actions should be collectively implemented to be effective. (author) [Spanish] El C-14 es un isotopo radiactivo del C con un periodo de semidesintegracion igual a 5700 anios y que decae a N-14 por emision de radiacion beta. Se produce naturalmente en las altas capas de la atmosfera debido a la reaccion N-14(n,p)C-14 inducida por neutrones lentos de rayos cosmicos. El C-14 antropogenico se genero debido a los ensayos nucleares y actualmente es producido durante la operacion de los reactores nucleares. Una vez liberado se incorpora a la biosfera a traves del ciclo del carbono. A partir de los inicios del periodo industrial la relacion C-14/C-estable, y por ende la dosis debida a C-14 que recibiria la poblacion mundial, ha variado continuamente. El objetivo del presente trabajo es presentar y analizar los distintos factores antropogenicos que modifican la concentracion de C-14, en particular el efecto Suess y la generacion de energia nuclear. Se observa que las

Effects of the TiC Nanoparticle on Microstructures and Tensile Properties of Selective Laser Melted IN718/TiC Nanocomposites

Science.gov (United States)

Yao, Xiling; Moon, Seung Ki; Lee, Bing Yang; Bi, Guijun

2018-03-01

The purpose of this paper is to investigate the effects of TiC nanoparticle content on microstructures and tensile properties of the IN718/TiC nanocomposites fabricated by selective laser melting (SLM). 0.5wt%, 1.0wt%, and 2.0wt% of TiC nanoparticles are added to the IN718 powders. The bulk-form IN718/TiC nanocomposites with different TiC contents are fabricated in-situ by SLM using the same process settings. The evolution of microstructures and tensile properties as the effect of changing the TiC content is studied using the optical microscopy, scanning electron microscopy, X-ray diffraction analysis, and tensile testing. The increase of TiC content refines the microstructure, promotes the formation of the cellular morphology, and reduces the size and continuity of Laves precipitates. Increasing the TiC content improves the yield strength and ultimate tensile strength but decreases the ductility. The grain refinement, dislocation bowing, dislocation punching, and the reduction in Laves precipitate contribute to the strengthening effect in the IN718/TiC nanocomposites.

Transfer of 14C to prenatal and neonatal rats from their mothers exposed to 14C compounds by ingestion

International Nuclear Information System (INIS)

Takeda, H.; Fuma, S.; Miyamoto, K.; Kuroda, N.; Inaba, J.

2003-01-01

The transfer of 14 C through placenta or milk was investigated and the radiation dose to fetal and newborn rats was estimated. Female rats at gestational stages or after delivery were exposed to 14 C in the form of sodium bicarbonate, thymidine and lysine by a single ingestion. Radioactivity in maternal tissues and conceptuses (placenta, fetal membrane and fetus) and in the newborn was determined at various times after ingestion. After exposure to these 14 C compounds, there was no significant difference between the 14 C concentration in the fetus and that in the maternal tissues, suggesting that the placenta has no effect in preventing or accelerating the placental transfer of 14 C. The concentration and content of 14 C in the fetus and newborn were, however, dependent on the chemical form of 14 C and on the prenatal or neonatal stage at the time of ingestion. The result of the dose estimation showed that 14 C-lysine gave significantly higher prenatal and neonatal doses than 14 C-sodium bicarbonate or 14 C-thymidine. (author)

Simultaneous measurement of cholesterol 7 alpha-hydroxylase activity by reverse-phase high-performance liquid chromatography using both endogenous and exogenous [4-14C]cholesterol as substrate

International Nuclear Information System (INIS)

Hylemon, P.B.; Studer, E.J.; Pandak, W.M.; Heuman, D.M.; Vlahcevic, Z.R.; Chiang, J.Y.

1989-01-01

The HPLC-spectrophotometric method for measuring cholesterol 7 alpha-hydroxylase activity was modified by using a C-18 reverse-phase column to separate 7 alpha-hydroxy-4-cholesten-3-one and 4-cholesten-3-one and by adding 7 beta-hydroxycholesterol to each reaction mixture as an internal recovery standard. With this method, we were able to simultaneously measure cholesterol 7 alpha-hydroxylase activity using endogenous cholesterol and exogenous [4- 14 C]cholesterol as substrate. Rat liver cytosol differentially stimulated (286%) the 7 alpha-hydroxylation of exogenous [4- 14 C]-cholesterol. In contrast, total cholesterol 7 alpha-hydroxylase activity was stimulated only 35% by cytosol. This method should prove useful for studying mechanisms of cholesterol delivery to cholesterol 7 alpha-hydroxylase

Correlative theoretical and experimental investigation of the formation of AlYB_1_4 and competing phases

International Nuclear Information System (INIS)

Hunold, Oliver; Chen, Yen-Ting; Music, Denis; Baben, Moritz to; Achenbach, Jan-Ole; Keuter, Philipp; Schneider, Jochen M.; Persson, Per O. Å.; Primetzhofer, Daniel

2016-01-01

The phase formation in the boron-rich section of the Al-Y-B system has been explored by a correlative theoretical and experimental research approach. The structure of coatings deposited via high power pulsed magnetron sputtering from a compound target was studied using elastic recoil detection analysis, electron energy loss spectroscopy spectrum imaging, as well as X-ray and electron diffraction data. The formation of AlYB_1_4 together with the (Y,Al)B_6 impurity phase, containing 1.8 at. % less B than AlYB_1_4, was observed at a growth temperature of 800 °C and hence 600 °C below the bulk synthesis temperature. Based on quantum mechanical calculations, we infer that minute compositional variations within the film may be responsible for the formation of both icosahedrally bonded AlYB_1_4 and cubic (Y,Al)B_6 phases. These findings are relevant for synthesis attempts of all boron rich icosahedrally bonded compounds with the space group: Imma that form ternary phases at similar compositions.

Correlative theoretical and experimental investigation of the formation of AlYB{sub 14} and competing phases

Energy Technology Data Exchange (ETDEWEB)

Hunold, Oliver, E-mail: hunold@mch.rwth-aachen.de; Chen, Yen-Ting; Music, Denis; Baben, Moritz to; Achenbach, Jan-Ole; Keuter, Philipp; Schneider, Jochen M. [Materials Chemistry, RWTH Aachen University, Kopernikusstr. 10, D-52074 Aachen (Germany); Persson, Per O. Å. [Department of Physics, Chemistry and Biology (IFM), Linköping University, S-58183 Linköping (Sweden); Primetzhofer, Daniel [Department of Physics and Astronomy, Uppsala University, Lägerhyddsvägen 1, S-75120 Uppsala (Sweden)

2016-02-28

The phase formation in the boron-rich section of the Al-Y-B system has been explored by a correlative theoretical and experimental research approach. The structure of coatings deposited via high power pulsed magnetron sputtering from a compound target was studied using elastic recoil detection analysis, electron energy loss spectroscopy spectrum imaging, as well as X-ray and electron diffraction data. The formation of AlYB{sub 14} together with the (Y,Al)B{sub 6} impurity phase, containing 1.8 at. % less B than AlYB{sub 14}, was observed at a growth temperature of 800 °C and hence 600 °C below the bulk synthesis temperature. Based on quantum mechanical calculations, we infer that minute compositional variations within the film may be responsible for the formation of both icosahedrally bonded AlYB{sub 14} and cubic (Y,Al)B{sub 6} phases. These findings are relevant for synthesis attempts of all boron rich icosahedrally bonded compounds with the space group: Imma that form ternary phases at similar compositions.

Incorporation of 2(S)-methylbutanoic acid-1-14C into the structure of mevinolin

International Nuclear Information System (INIS)

Willard, A.K.; Smith, R.L.

1982-01-01

A route to mevinolin approximately equal to (1) bearing (S)-2-methylbutanoic acid -1- 14 C as the ester side chain has been developed. The structure of mevinolin approximately equal to (1) was degraded and selectively protected to provide the alcohol approximately equal to 3 in three steps. Incorporation of 14 C was accomplished by acylation of alcohol approximately equal to 3 with (R,S)-2-methylbutyryl chloride-1- 14 C. Cleavage of the silyl ether protecting group in the resulting mixture of esters approximately equal to 4 provided the two diastereoisomers approximately equal to 5 and approximately equal to 6 which were separated by reverse-phase liquid chromatography. Mevinolin - 14 C approximately equal to (5) was also converted to the ammonium salt approximately equal to 7 of the corresponding dihydroxy acid. (author)

Delayed plasma clearance and hepatic uptake of lymph chylomicron 14C-cholesterol in marginally zinc-deficient rats

International Nuclear Information System (INIS)

Koo, S.I.; Algilani, K.; Norvell, J.E.; Henderson, D.A.

1986-01-01

Previously, chylomicrons from marginally zinc-deficient rats were shown to be abnormally large, with markedly reduced levels of apoproteins C and E. In the present study, effects of such changes on the plasma clearance and hepatic uptake of chylomicron cholesterol were investigated in rats fed 3 ppm of zinc (ZD), as compared with those fed 30 ppm of zinc (CT). The rate of plasma clearance was determined by plasma 14C-radioactivity at different intervals after intravenous injection of lymph chylomicrons labeled in vivo with 14C-cholesterol. The 14C-clearance curves were nonlinear, consisting of an initial rapid phase followed by a slow phase of clearance. The initial 14C-clearance was significantly (p less than 0.05) delayed whether the labeled chylomicrons from ZD donors were injected into ZD or CT recipients. The hepatic 14C-recovery in extracted lipids was also significantly lower in ZD rats. The present data provide first evidence that a marginal level of zinc deficiency produces a significant delay in the plasma clearance and hepatic uptake of chylomicron cholesterol. This may be attributable in part to the molecular alterations of chylomicrons induced by zinc deficiency

Root-uptake of {sup 14}C derived from acetic acid and {sup 14}C transfer to rice edible parts

Energy Technology Data Exchange (ETDEWEB)

Ogiyama, Shinichi [Office of Biospheric Assessment for Waste Disposal, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba-shi 263-8555 (Japan)], E-mail: ogiyama@nirs.go.jp; Suzuki, Hiroyuki [Graduate School of Pharmaceutical Sciences, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba-shi 263-5522 (Japan); Inubushi, Kazuyuki [Graduate School of Horticulture, Chiba University, 648 Matsudo, Matsudo-shi 271-8510 (Japan); Takeda, Hiroshi; Uchida, Shigeo [Office of Biospheric Assessment for Waste Disposal, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba-shi 263-8555 (Japan)

2010-02-15

Three types of culture experiments using paddy rice (Oryza sativa L.) were performed to examine root-uptake of {sup 14}C in the form of acetic acid: double pot experiment (hydroponics), wet culture experiment (submerged sand medium), and chamber experiment (hydroponics and submerged sand medium). The {sup 14}C radioactivity in the plant, mediums, and atmospheric carbon dioxide ({sup 14}CO{sub 2}) in the chamber were determined, and the distribution of {sup 14}C in the plant was visualized using autoradiography. In the double pot experiment, the shoot of the plant and the lower root which was soaked in the culture solution had {sup 14}C radioactivity, but the upper root which did not have contact with the solution had none. There were also {sup 14}C radioactivity in the grains and roots in the wet culture experiment. Results of the chamber experiment showed that {sup 14}CO{sub 2} gas was released from the culture solution in both types of cultures. Results indicated that the {sup 14}C-acetic acid absorbed by rice plant through its root would be very small. Most of the {sup 14}C-acetic acid was transformed into gaseous forms either in the culture solution or rhizosphere. A relatively longer time would be needed to assimilate {sup 14}C derived from acetic acid to grain parts after it was once absorbed by the shoot through the root. Availability of {sup 14}C for the plant in sand culture was considered to be decreased compared with that for the plant in the hydroponics experiment. It was suggested that rice plant absorbed and assimilated {sup 14}C through the plant roots not because of uptake of {sup 14}C-acetic acid but because of uptake of {sup 14}C in gaseous forms such as {sup 14}CO{sub 2}.

Method of preparing D-mannose(U-14C) from glucons(U-14C) separated from natural material

International Nuclear Information System (INIS)

Kucar, S.; Zemek, J.; Bilik, V.; Kolina, J.

1981-01-01

Glucans(U- 14 C) separated from green or blue-green algae are hydrolysed using diluted mineral acids in the presence of small amounts of molybdate ions to D-glucose(U- 14 C) which, at a temperature of 60 to 100 degC epimerizes to D-mannose(U- 14 C). The epimeric aldoses are separated from the reaction mixture by paper chromatography. (H.S.)

Uptake and translocation of [14C]-monoethanolamine in barley plants

International Nuclear Information System (INIS)

Eckert, H.; Bergmann, H.; Reissmann, P.

1988-01-01

Uptake and translocation of 14 C-monoethanolamine (EA) and its hydrochloride were investigated after application to an unwounded part of the fifth leaf from the main shoot of intact spring barley plants. After 48 and 72 h, resp., the free EA base was both absorbed rapidly and translocated out of the feeding leaf. The absorbed 14 C preferably migrated to the tillers, which resulted in an approximately uniform distribution of the radioactivity in the above ground parts of the plant after the uptake phase (similar 14 C concentrations in the main shoot and tillers), whereas only few radioactivity moved to the roots. On the other hand, the protonated EA (EA-HCl) exhibited both a reduced uptake and a restricted mobility. The bulk of radioactivity remained in the main shoot. As a consequence of the principally analogous metabolism of EA and its protonated form, the translocation differences are compensated during ontogenesis. When the plants reached maturity, similar distribution patterns could be found in which the kernels represented a considerable sink. (author)

The Al-rich region of the Al-Mn-Ni alloy system. Part II. Phase equilibria at 620-1000 oC

International Nuclear Information System (INIS)

Balanetskyy, S.; Meisterernst, G.; Grushko, B.; Feuerbacher, M.

2011-01-01

Research highlights: → Phase equilibria in the Al-rich region of the Al-Mn-Ni alloy system were studied at 1000, 950, 850, 750, 700, 645 and 620 deg. C by means of SEM, TEM, powder XRD and DTA. → Three ternary thermodynamically stable intermetallics, the φ-phase (Al 5 Co 2 -type, hP26, P63/mmc; a = 0.76632(16), c = 0.78296(15) nm), the κ-phase (κ-Al 14.4 Cr 3.4 Ni l.1 -type, hP227, P63/m; a = 1.7625(10), c = 1.2516(10) nm), and the O-phase (O-Al 77 Cr 14 Pd 9 -type, Pmmn, oP650,: a = 2.3316(16), b = 1.2424(15), c = 3.2648(14) nm), as well as three ternary metastable phases, the decagonal D 3 -phase with periodicity about 1.25 nm, the Al 9 (Mn,Ni) 2 -phase (Al 9 Co 2 -type, P1121/a, mP22; a = 0.8585(16), b = 0.6269(9), c = 0.6205(11) nm, β = 95.34(10) o ) and the O 1 -phase (basecentered orthorhombic, a ∼ 23.8, b ∼ 12.4, c ∼ 32.2 nm) were revealed. → The existence of a thermodynamically stable R-phase of stoichiometry Al 60 Mn 11 Ni 4 , reported earlier in literature, was not confirmed in the present study. - Abstract: Phase equilibria in the Al-rich region of the Al-Mn-Ni alloy system were studied at 1000, 950, 850, 750, 700, 645 and 620 o C. Three ternary thermodynamically stable intermetallics, the φ-phase (Al 5 Co 2 -type, hP26, P6 3 /mmc; a = 0.76632(16), c = 0.78296(15) nm), the κ-phase (κ-Al 14.4 Cr 3.4 Ni l.1 -type, hP227, P6 3 /m; a = 1.7625(10), c = 1.2516(10) nm), and the O-phase (O-Al 77 Cr 14 Pd 9 -type, Pmmn, oP650,: a = 2.3316(16), b = 1.2424(15), c = 3.2648(14) nm), as well as three ternary metastable phases, the decagonal D 3 -phase with periodicity about 1.25 nm, the Al 9 (Mn,Ni) 2 -phase (Al 9 Co 2 -type, P112 1 /a, mP22; a = 0.8585(16), b = 0.6269(9), c = 0.6205(11) nm, β = 95.34(10) o ) and the O 1 -phase (base-centered orthorhombic, a ∼ 23.8, b ∼ 12.4, c ∼ 32.2 nm) were revealed. Their physicochemical behaviour in the Al-Mn-Ni alloy system was studied.

Model experiments for {sup 14}C water-age determinations

Energy Technology Data Exchange (ETDEWEB)

Wendt, I; Stahl, W; Geyh, M; Fauth, F [Bundesanstalt fuer Bodenforschung, Hannover (Germany)

1967-05-15

{sub 2} phase. A correction for the initial {sup 14}C-activity by means of the {delta}{sup 13}C-value is no longer possible, and the reliability of the {sup 14}C-dating method becomes questionable. (author)

14C Records from Indonesian Sea

International Nuclear Information System (INIS)

Baresic, J.; Fallon, S.; Mazerat, J.

2013-01-01

To investigate ocean currents and past climate events affecting the Indonesian throughflow (ITF), a radiocarbon record from a Porites coral collected from Alor Island, Indonesia, was constructed. Porites corals are often used in paleoclimate research and water mass circulation studies in the Tropics because of their abundance in the region and growth rate of 8 - 20 mm/y. These characteristics allow reconstructions of past environmental changes on weekly to annual time scales. At this point radiocarbon coral results from Alor cover approximately 30 years. An age model was constructed using the sea surface temperature proxy δ18O. Alor radiocarbon results were compared with previous measurements obtained from Padang and Langkai corals. a14C values obtained from the Alor coral display a strong seasonal cycle, high values during Australian summer and low values during Australian winter. Higher a 14C summer values indicate inflow of waters enriched by 14C through Makassar Strait from the North Pacific Ocean and Java Sea surface water. Summer a14C values are also enhanced by summer stratification. Winter values indicate upwelling of deep Ocean waters within the research area and transport of 14C-depleted waters from the Banda Sea, which has input from the South Pacific Ocean (lower a14C than North Pacific). Therefore, the a14C coral record reflects the movement of enriched water from North Pacific to Indian Ocean through Makassar Strait during summer and upwelling of depleted surface waters from the Banda Sea during the winter. Lower a14C dips could be attributed to strong El Nino events, which would enhance surface water mixing and upwelling of low radiocarbon deep waters. Water transport from North Pacific Ocean decreases during El Nino events also contributing to lowering of a14C signal.(author)

Synthesis of C-9-14C-1,8-dihydroxy-3-carboxyanthraquinone

International Nuclear Information System (INIS)

De Witte, P.; Lemli, J.

1988-01-01

The synthesis of C-9- 14 C-rhein is reported using 14 CO 2 as a 14 C-source. After preparing 14 C-1, 8-dimethoxy-3-methylanthraquinone by a condensation reaction, the product is demethylated and the 3-methyl group converted to the corresponding 3-carboxy group. The radio-active yield of the total synthesis, starting with 1 Ci 14 CO 2 is 6,9% (6, 9 mCi); 352 mg 14 rhein is produced with a specific activity of 55,7 mCi/mmol. (author)

Synthesis of [14C]-62514, a radiolabelled derivative of erythromycin A, via [2-14C]N,N-dimethylethylenediamine

International Nuclear Information System (INIS)

Surber, B.W.; Baker, W.R.; Seif, L.

1991-01-01

The synthesis of [ 14 C]A-62514, 11-deoxy-11[carboxy(2-dimethylamino-[1- 14 C]ethyl)amino]-6-0-methyl-e rythromycin A 11,12-(cyclic ester), was performed in five steps. The key intermediate, [2- 14 C]N,N-dimethylethyl-enediamine, was obtained in 80% yield by reacting Eschenmoser's salt with K 14 CN and reducing the resulting [1- 14 C]N,N-dimethylglycinonitrile with H 2 and Raney Ni in methanol and ammonium hydroxide. The final product was obtained 97% radiochemically pure in an overall radiochemical yield of 14%, with a specific activity of 39 mCi/mmol. (author)

The 14C-labelling of 2-chloroethyl isocyanate. Application to the labelling of chloroethyl tetrazinone and chloroethylnitrosoureas

International Nuclear Information System (INIS)

Madelmont, J.C.; Moreau, M.F.; Godeneche, D.; Labarre, P.; Veyre, A.

1988-01-01

The labelling of 2-chloroethyl isocyanate with 14 C on the carbonyl group from 3-chloro [carboxyl- 14 C] propionic acid is described. The Curtius reaction under phase transfer condition was used. This isocyanate was used to synthesize 2-chloroethyl tetrazinone and 2-chloro-ethyl nitrosourea. (author)

Synthesis of DL-adrenaline (methyl C{sup 14}) (1961); Synthese de la DL-adrenaline (methyle {sup 14}C) (1961)

Energy Technology Data Exchange (ETDEWEB)

Pichat, L; Audinot, M [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1961-07-01

The sodium derivative of 5-3-4 dibenzyl oxyphenyl 2-oxazolidinone reacted with methyl iodide {sup 14}C, in stoichiometric quantity, gives rise to the corresponding N-methyl {sup 14}C derivative. The oxazolidinone ring is opened by concentrated hydrochloric acid and the benzyl groups removed by catalytic hydrogenolysis. Adrenaline methyl {sup 14}C is then purified on Dowex 50 X-12 exchange resin. Overall-yield is 45 per cent based upon methyl iodide {sup 14}C. (author) [French] Le derive sode de la (dibenzyloxy-3-4-phenyl)-5 oxazolidinone-2 traite par l'iodure de methyle {sup 14}C, en proportion stoechiometrique, fournit le derive N-methyle {sup 14}C correspondant. Apres ouverture du cycle oxazolidinone par HCL concentre et debenzylation par hydrogenation catalytique, on purifie l'adrenaline (methyle {sup 14}C) par chromatographie sur resine echangeuse Dowex 50 X-12. Le rendement est de 45 pour cent par rapport a l'iodure de methyle {sup 14}C. (auteurs)

Synthesis of DL-adrenaline (methyl C{sup 14}) (1961); Synthese de la DL-adrenaline (methyle {sup 14}C) (1961)

Energy Technology Data Exchange (ETDEWEB)

Pichat, L.; Audinot, M. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1961-07-01

The sodium derivative of 5-3-4 dibenzyl oxyphenyl 2-oxazolidinone reacted with methyl iodide {sup 14}C, in stoichiometric quantity, gives rise to the corresponding N-methyl {sup 14}C derivative. The oxazolidinone ring is opened by concentrated hydrochloric acid and the benzyl groups removed by catalytic hydrogenolysis. Adrenaline methyl {sup 14}C is then purified on Dowex 50 X-12 exchange resin. Overall-yield is 45 per cent based upon methyl iodide {sup 14}C. (author) [French] Le derive sode de la (dibenzyloxy-3-4-phenyl)-5 oxazolidinone-2 traite par l'iodure de methyle {sup 14}C, en proportion stoechiometrique, fournit le derive N-methyle {sup 14}C correspondant. Apres ouverture du cycle oxazolidinone par HCL concentre et debenzylation par hydrogenation catalytique, on purifie l'adrenaline (methyle {sup 14}C) par chromatographie sur resine echangeuse Dowex 50 X-12. Le rendement est de 45 pour cent par rapport a l'iodure de methyle {sup 14}C. (auteurs)

The effect of alloying elements on the creep and impact properties of high Cr steels

International Nuclear Information System (INIS)

Kim, S. H.; Song, B. J.; Ryu, W. S.

2000-01-01

The effect of minor alloying elements on the creep and impact properties in high Cr steels has been studied. The addition of W and N in creased the creep rupture strength without the decrease of the impact toughness. During deformation, growth of lath width and agglomeration of precipitates and precipitation of Laves phase occurred. These microstructural changes made the steels soften. The degree of softening was delayed by the addition of W and N. In W added steel, the Laves phase had a important role in increasing the creep rupture strength. But the impact toughness was rapidly degraded by the addition of W after aging at 600 .deg. C for 5000 hours. So it needs to evaluate more accurately the effect of Laves phase on creep and impact properties. In N added steel, V(C,N) was precipitated in lath boundary and interior of lath. The size of the precipitates was 20-50nm. The increase of creep rupture strength in N added steel may be due to the precipitate of the V(C,N). So it needs more test to clarify the effect of N on the creep and impact properties

Synthesis of ethanol {sup 14}C-1; Synthese d'ethanol {sup 14}C-1

Energy Technology Data Exchange (ETDEWEB)

Wolff, R E; Pichat, L [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1958-07-01

The direct reduction by LiAlH{sub 4}, of a suspension of anhydrous sodium acetate in tetra-hydro-furfuryl-oxy-tetra-hydro-pyran is described. This study has shown that the ethanol thus obtained is impure and that the yields are erratic. On the contrary the reduction of acetyl chloride 1-{sup 14}C by LiAlH{sub 4}, in 'diethyl carbitol' leads to ethanol 1-{sup 14}C of satisfactory purity with a yield of about 71 percent. (author) [French] Une etude de la reduction directe par LiAlH{sub 4}, de l'acetate de soude anhydre en suspension dans le tetrahydrofurfuryloxytetrahydropyrane est decrite. Cette etude a montre que l'on obtient de l'ethanol souille d'impuretes, avec un rendement variable. Par contre, la reduction du chlorure d'acetyle {sup 14}C-1 par LiAlH{sub 4}, dans le 'diethyl carbitol' conduit a l'ethanol {sup 14}C-1 de purete convenable avec un rendement de l'ordre de 71 pour cent. (auteur)

Elimination of the 12 C and 16 O in the elastic scattering of 14 C by polarized protons

International Nuclear Information System (INIS)

Avila A, O.L.; Ramirez T, J.J.; Murillo O, G.; Fernandez B, M.

1991-04-01

The study of the elastic scattering of 14 C for polarized protons it provides information on the nuclear structure of 15 N. In the Tandem accelerator of the Nuclear Center in collaboration with the University of Notre Dame is carrying out this study to energy between 5.0 and 9.0 MeV in steps of 10 keV. The measures of differential section and vectorial analyzer power are subjected to shift analysis of phase being able to determine the parameters of the excited levels of 15 N that are it angular momentum, parity, level width and elastic width. The details of this experiment are presented in the ACEL-9102 technical report while in this work it was discussed the way in that contributions of 12 C and 16 O are eliminated that are present as impurities in our target of 14 C. At small angles the elastic components of these impurities are shoveled with the elastic of 14 C. In the experiment carried out in the Nuclear Center were take measures of differential section for 6 angles; 35, 45, 55, 65, 145 and 165 using surface barrier detectors. It is observed that it exists shovels at 35, 45, 55 and 65 while at 145 and 165 the 12 C, the 14 C and the 16 O are totally separate. With the purpose of being able to subtract of the elastic of 14 C the proportion of 12 C, it was decided to bombard a target of 12 C leaving the same geometry that had been used to bombard 14 C. With this also carried out the reaction 12 C (p,p) 12 C between 5.0 and 9.0 MeV in steps of 50 keV. Starting from these spectra are the integration (yield) of the elastic of 12 C. (Author)

Neutron irradiation effects in advanced superconductors

International Nuclear Information System (INIS)

Yoshida, H.; Kodaka, H.; Miyata, K.; Hayashi, Y.; Atobe, K.

1988-01-01

This paper reports the effects of neutron irradiation on superconducting transitions studied by susceptibility and resistivity measurements for A15 type compounds, Laves-phase compounds and oxide superconductors. For A15 superconductors, the transition temperature (T c ) decreased with increasing neutron fluence and showed large drop started at about 5 x 10 18 n/cm 2 (E > 0.1 MeV). Post-irradiation annealing gave recovery of T c , but the behaviors were different for the materials with different composition and microstructure. The Laves-phase compounds showed less degradation than the A15 superconductors. For oxide superconductors very sensitive transition change was observed, including the radiation-induced superconductivity

Metabolic kinetics and biological effects of radiocarbon (14C)

International Nuclear Information System (INIS)

Vasilenko, I.Ya.; Osipov, V.A.; Lyaginskaya, A.M.; Bugryshev, P.F.; Istomina, A.G.; Turova, V.I.; Dement'ev, S.I.; Zhorova, E.S.; Mart'yanov, B.M.; Shal'nova, G.A.; Kuz'mina, T.D.; Shebenko, V.A.; Pomerantseva, M.D.; Ramajya, L.K.

1988-01-01

Radiocarbon 14 C is one of the most widespread radionuclides. Increased concentration of anthropogenic 14 C in the biosphere is a problem of considerable hygienic and ecological significance. The paper presents the results of comprehensive studies for years on biokinetics of the main 14 C compounds, inorganic (Na H 14 CO 3 , Na 2 14 CO 3 , K 2 14 CO 3 , Ca 14 CO 3 ) as well as organic ( 14 C-glucose, 14 C-succinic acid, 14 C-glucosamine, 14 C-glycine, 14 C-tryptophane, 14 C-valine, 14 C-palmitic acid, 14 C-stearic acid, 14 C-ethyl alcohol, 14 C-methyl alcohol, 14 C-urea), of 14 C as food constituent and of elementary radiocarbon. The 14 C toxicity is investigated for both acute and chronic small doses received by animals. The nuclide's genetic efficiency is assessed. Based on research evidence, the accumulation multiple and equilibrium time are estimated for long-term 14 C intake by humans. The data may be used for setting genetic standards and estimating an anthropogenic increase of 14 C concentration in the environment. The hazard of anthropogenic radiocarbon is assessed with allowance for further development of nuclear power industry. (author)

S-adenosyl-L-(l-14C)-homocysteine

International Nuclear Information System (INIS)

Thomas, H.J.; Montgomery, J.A.

1987-01-01

S-Adenosyl-L-(1- 14 C)-homocysteine was prepared from commercially available L-(1- 14 C)-methionine by conversion first to S-benzyl-L-(1- 14 C)-homocysteine which upon treatment with sodium in liquid ammonia gave the disodium salt of L-(1- 14 C)-homocysteine. Reaction of this sodium salt with 5'-O-tosyladenosine gave the title compound. (author)

Nd2Fe14C-based magnet with better permanent magnetic properties prepared by a simple mechanochemical method

Science.gov (United States)

Geng, Hongmin; Ji, Yuan; Zhang, Jingjing; Gao, Yuchao; Yan, Yu; Wang, Wenquan; Su, Feng; Du, Xiaobo

2017-11-01

Nd2Fe14C-based magnet is prepared by a mechanochemical method, namely high-energy ball-milling Nd2Fe11Bx (x = 0-0.15) alloy in heptane (C7H16), followed by annealing to 850 °C in vacuum. Under the action of high-energy ball-milling, Nd2Fe11Bx react with heptane to form NdH2+δ, Fe-(CB), C, etc. H2 is released and Nd2Fe17, Nd2Fe17Cx (x = 0-3), Nd2Fe14C, Nd carbides and α-Fe are formed in the subsequent annealing. C amount depends on ball-milling time t. Long time ball milling or high C content suppresses the formation of 2:17 phase and favors the formation of 2:14:1 phase in the final products. Excessive ball-milling results in the quick increase of α-Fe. The maximum of magnetically hard Nd2Fe14C is obtained at t = 4 h. For Nd2Fe11 samples, there exists considerable quantity of Nd carbides and α-Fe phase appears earlier and increases rapidly with extending the ball-milling time t. The addition of B element shortens the ball-milling time of the formation of maximum Nd2Fe14C and prominently suppresses the formation of Nd carbide and α-Fe. The optimum magnetic properties, coercivity iHc of 1193.7 kA/m, remanence Mr of 580.9 kA/m, maximum magnetic energy product (BH)max of 91.7 kJ/m3 is approaching to its theoretic value of 99.2 kJ/m3 for isotropic Nd2Fe14C magnet, are obtained in Nd2Fe11B0.06 alloy ball milled for 3.5 h.

C18, C8, and perfluoro reversed phases on diamond for solid-phase extraction.

Science.gov (United States)

Saini, Gaurav; Wiest, Landon A; Herbert, David; Biggs, Katherine N; Dadson, Andrew; Vail, Michael A; Linford, Matthew R

2009-04-17

In spite of advances in solid-phase extraction (SPE) technology there are certain disadvantages to current SPE silica-based, column packings. The pH range over which extraction can occur is limited and each column is generally only used once. New diamond-based reversed SPE phases (C(18), C(8), and perfluorinated) were developed in our laboratories. Studies were done which show that these phases do not have the same limitations as traditional silica-based stationary phases. The synthesis and properties of these diamond-based phases are presented, and the stability, percent recovery, and column capacity are given for the C(18) phase.

Synthesis of /sup 14/C-labeled felbamate from phenylacetic-(methylene-/sup 14/C) acid

Energy Technology Data Exchange (ETDEWEB)

Choi, Y.M.; Kucharczyk, N.; Sofia, R.D.

1986-05-01

A synthetic procedure for the preparation of 2-phenyl-1,3-propanediol-2-/sup 14/C dicarbamate, starting with phenylacetic-(methylene-/sup 14/C) acid was developed. The procedure from phenylacetic acid to 2-phenyl-1,3-propanediol dicarbamate has four steps via phenylmalonic acid and 2-phenyl-1,3-propanediol. The overall yield of all four steps was 28%.

Microstructural evolution and creep of Fe-Al-Ta alloys

Energy Technology Data Exchange (ETDEWEB)

Prokopcakova, Petra; Svec, Martin [Technical University of Liberec (Czech Republic). Dept. of Material Science; Palm, Martin [Max-Planck-Institut fuer Eisenforschung GmbH, Duesseldorf (Germany). Structure and Nano-/Micromechanics of Materials

2016-05-15

The microstructural evolution in Fe-Al-Ta alloys containing 23 - 31 at.% Al and 1.5 - 2.2 at.% Ta has been studied in the temperature range 650 - 750 C by annealing for 1, 10, 100 and 1 000 h. The experiments confirm that in this temperature range the precipitation of the stable hexagonal C14 Laves phase is preceded by formation of coherent, metastable L2{sub 1} Heusler phase precipitates within the Fe-Al matrix. However, precipitates of C14 are observed after much shorter annealing times than previously assumed. Creep strength increases substantially with increasing Al content of the alloys because the solid solubility for Ta in the Fe-Al matrix increases with increasing Al content and solid-solution hardening contributes substantially to the observed high creep strength. It may therefore be that the microstructural changes during creep have no noticeable effect on creep strength.

Microstructural evolution and creep of Fe-Al-Ta alloys

International Nuclear Information System (INIS)

Prokopcakova, Petra; Svec, Martin; Palm, Martin

2016-01-01

The microstructural evolution in Fe-Al-Ta alloys containing 23 - 31 at.% Al and 1.5 - 2.2 at.% Ta has been studied in the temperature range 650 - 750 C by annealing for 1, 10, 100 and 1 000 h. The experiments confirm that in this temperature range the precipitation of the stable hexagonal C14 Laves phase is preceded by formation of coherent, metastable L2 1 Heusler phase precipitates within the Fe-Al matrix. However, precipitates of C14 are observed after much shorter annealing times than previously assumed. Creep strength increases substantially with increasing Al content of the alloys because the solid solubility for Ta in the Fe-Al matrix increases with increasing Al content and solid-solution hardening contributes substantially to the observed high creep strength. It may therefore be that the microstructural changes during creep have no noticeable effect on creep strength.

Direct preparation of 14C-labelled 5-allyl- and 5-propyl-2'-deoxyuridine from [2-14C]2'-deoxyuridine

International Nuclear Information System (INIS)

Ruth, J.L.; White, S.K.; Bergstrom, D.E.

1982-01-01

[2- 14 C]5-Allyl-2'-deoxyuridine was synthesized directly from [2- 14 C]2'-deoxyuridine using mercury, palladium, and 3-chloropropene. [2- 14 C]5-Propyl-2'-deoxyuridine was obtained by hydrogenation of the [ 14 C]5-allyl-2'-deoxyuridine. Advantages of the synthetic method and its application to the preparation of other radiolabeled 5-alkyl/alkenyl-2'-deoxyuridines are discussed. (author)

Synthesis of [14C]Zolpidem

International Nuclear Information System (INIS)

Allen, J.; Tizot, A.

1986-01-01

The synthesis of [ 14 C]Zolpidem, a new hypnotic agent having a non-benzodiazepine structure, is described. This compound was synthesised in a 64% overall radiochemical yield from potassium [ 14 C]cyanide and with a specific radioactivity of 56 mCi/mmol. It was used for pharmacokinetic and drug metabolism studies. (author)

A convenient method for 14C-labeling of 2-methylthio-1-[4-N-α-ethoxycarbonylbenzyl)-amino-benzyl] -5-hydroxymethyl-2-[14C]-1H-imidazole and 1-[4-N-α-ethoxy-carbonylbenzyl)-aminobenzyl]-5-hydroxymethyl-2-[14C] -1H-imidazole as potential antihypertensives

International Nuclear Information System (INIS)

Nader Saemian; Gholamhossein Shirvani; Mohsen Javaheri; Sayed Sajad Oliyaee

2012-01-01

The key synthetic intermediate, (2-mercapto-1-(4-nitrobenzyl)-1H-imidazol-5-yl)methanol-[2- 14 C], has been synthesized by using one pot procedure from potassium[ 14 C]-thiocyanate. It was converted to two nonpeptide angiotensin II receptor antagonists, 2-methylthio-1-[4-N-α-ethoxycarbonyl benzyl)-aminobenzyl]-5-hydroxymethyl-1H-imidazole-[2- 14 C] and 1-[4-N-α-ethoxy-carbonylbenzyl)-aminobenzyl] -5-hydroxymethyl-1H-imidazole-[2- 14 C] via a 3-step sequence synthetic pathway. (author)

Effective Exploration of New 760°C-Capability Steels for Coal Energy

Energy Technology Data Exchange (ETDEWEB)

Clark, Williams [The Ohio State Univ., Columbus, OH (United States); Zhao, Ji-Cheng [The Ohio State Univ., Columbus, OH (United States)

2016-09-17

Cost effective and high performance alloys that are capable of operating at 760 °C or higher for extended periods of time under a very aggressive environment are critically required for the design and development of advanced ultrasupercritical (AUSC) boilers and steam turbines. Finely dispersed Laves phase precipitates have been shown by Takeyama and co-workers to be a viable strengthening mechanism in high temperature austenitic steels. There is currently no straightforward theory that can predict what other intermetallic phases can serve as potent precipitation-strengthening phases for steels; thus we employed a highly effective dual-anneal diffusion multiple (DADM) approach to screen for viable strengthening precipitates over a wide range of compositions. From the Fe-Co-Cr-Ni-Mo DADMs, the Fe-Cr-Mo based Chi phase was identified as a new strengthening phase for high temperature ferritic steels; and from the Fe-Mn-Cr-Nb-Ni-Mo-FeAl DADMs, the Laves phase was identified as a viable strengthening precipitate in Fe-Mn and Fe-Ni based austenitic steels. After identification of viable strengthening phases from the DADMs that covered compositions in the basic ternary and quaternary systems, we employed computation thermodynamics to perform multicomponent alloy design and optimization. For the new the Chi-phase strengthened steels, we performed thermodynamic calculations to vary the volume fraction of the Chi phase and introduced Nb and carbon to promote the formation of stable carbides for grain size control during solution heat treatment. For the Fe-Ni-Mn based austenitic steels, we performed extensive parametric optimization of compositions in order to reduce the expensive Ni content, add Cr and Al for oxidation resistance, and balance the alloying contents (Ni, Mn, Cr, Al, Mo) to suppress the ferritic phase and promote the austenitic matrix phase. Four steels (two ferritic + two austenitic) were designed and tested. The two Chi-phase strengthened ferritic steels

C -14 analysis in radioactive waste by combustion and digestion techniques

International Nuclear Information System (INIS)

Venescu, R. E.; Valeca, M.; Bujoreanu, L.; Bujoreanu, D.; Venescu, B.

2016-01-01

Carbon-14 is a long lived radionuclide (half life of 5730 years) present in almost all radioactive waste streams generated by a CANDU nuclear power plant. It is a pure beta emitter that decays to 14N by emitting low energy beta-radiation with an average energy of 49.5keV and a maximum energy of 156keV. Before the beta radiation of 14C can be measured from radioactive waste liquid scintillation counting (LSC), the samples must be transformed in a stable, clear and homogeneous solution. Two methods were tested for carbon-14 recovery and analysis in radioactive wastes from nuclear power plants. The combustion process is a simple automatic method of sample preparation, in which all carbon isotopes, including 14C are oxidized to gaseous carbon dioxide that is subsequently trapped in form of carbonate in a column filled with a carbon dioxide absorbent. The microwave digestion is the method wherein the samples are transformed totally or partially in liquid phase depending on the sample matrix using adequate digestion reagents. The samples were counted with a normal and low level count mode liquid scintillation counter Tri-Carb3110TR. The tests performed on the simulated radwaste showed a 14C recovery of 90% by combustion and higher than 75% by microwave digestion method. (authors)

A rapid microwave induced synthesis of [carboxyl-14C]-nicotinic acid (vitamin B3) and [carbonyl-14C]-nicotinamide using K14CN

International Nuclear Information System (INIS)

Ravi, S.; Mathew, K.M.; Sivaprasad, N.

2008-01-01

Microwave assisted direct aromatic substitution of 3-bromopyridine with K 14 CN as the cyanide source and catalytic amount of tetrabutylammonium bromide afforded [3- 14 C]-cyanopyridine 3 in 90% yield. Microwave assisted hydrolysis of 3 with a mixture of concentrated hydrochloric acid and propionic acid afforded [carboxyl- 14 C]-nicotinic acid in 95% yield whereas microwave assisted hydrolysis of 3 with a mixture of concentrated sulfuric acid and propionic acid afforded [carbonyl- 14 C]-nicotinamide in 85% yield. (author)

Influence of Annealing on Microstructure and Mechanical Properties of Refractory CoCrMoNbTi0.4 High-Entropy Alloy

Science.gov (United States)

Zhang, Mina; Zhou, Xianglin; Zhu, Wuzhi; Li, Jinghao

2018-04-01

A novel refractory CoCrMoNbTi0.4 high-entropy alloy (HEA) was prepared via vacuum arc melting. After annealing treatment at different temperatures, the microstructure evolution, phase stability, and mechanical properties of the alloy were investigated. The alloy was composed of two primary body-centered cubic structures (BCC1 and BCC2) and a small amount of (Co, Cr)2Nb-type Laves phase under different annealing conditions. The microhardness and compressive strength of the heat-treated alloy was significantly enhanced by the solid-solution strengthening of the BCC phase matrix and newborn Laves phase. Especially, the alloy annealed at 1473 K (1200 °C) achieved the maximum hardness and compressive strength values of 959 ± 2 HV0.5 and 1790 MPa, respectively, owing to the enhanced volume fraction of the dispersed Laves phase. In particular, the HEAs exhibited promising high-temperature mechanical performance, when heated to an elevated temperature of 1473 K (1200 °C), with a compressive fracture strength higher than 580 MPa without fracture at a strain of more than 20 pct. This study suggests that the present refractory HEAs have immense potential for engineering applications as a new class of high-temperature structural materials.

Appraisal of the 14C-glycocholate acid test with special reference to the measurement of faecal 14C excretion

International Nuclear Information System (INIS)

Scarpello, J.H.B.; Sladen, G.E.

1977-01-01

The 14 C-glycocholate test, including the measurement of marker corrected faecal 14 C, has been assessed in the following groups of subjects: normal controls (18), patients with diarrhoea not attributable to altered bile acid metabolism (21), patients with diverticula of the small intestine (12), patients with previous resection of ileum and often proximal colon (34), and established ileostomists (10). Patients with diverticular disease had increased breath 14 CO 2 excretion, but normal faecal excretion of 14 C, and this test was more frequently abnormal than the Schilling test. Ileostomists excreted increased amounts of faecal 14 C, even when the ileum was intact and apparently normal. The pattern after resection was complex. Breath 14 C output was normal if the ileal resection was less than 25 cm in length, although some of these patients had increased faecal 14 C excretion if, in addition, at least 15 cm of proximal colon had been resected or by-passed. Longer ileal resections were associated with increased breath and/or faecal 14 C excretion, depending in part on the length of colon resected or by-passed and the 24 hour faecal volume. Fewer than half these patients had both increased breath and faecal excretion of isotope and faecal 14 C alone was occasionally normal with an ileal resection of 50 cm or more. The 14 C-glycocholate test was more frequently abnormal than the Schilling test in this group. The use of faecal marker correction had only a minor impact on the results. These data suggest that, in patients with ileal resection, faecal 14 C, like faecal weight, is determined by the extent of colonic resection as well as by the amount of ileum resected. (author)

Synthesis of 14C-labelled milrinone

International Nuclear Information System (INIS)

Duncan, D.R.; Johnston, D.; Andrews, R.S.

1985-01-01

A synthetic procedure for producing 14 C-labelled milrinone, a potent new cardiotonic agent, is described. The synthesis was achieved in two steps from 1-(4-pyridyl)propan-2-one utilising [2- 14 C]cyanoacetamide as the source of the radiolabel. The overall chemical yield was 46% and the radiochemical yield 35%. (author)

Behaviour of 14C-sulfadiazine and 14C-difloxacin during manure storage

International Nuclear Information System (INIS)

Lamshoeft, Marc; Sukul, Premasis; Zuehlke, Sebastian; Spiteller, Michael

2010-01-01

The persistence of sulfadiazine, difloxacin, and their metabolites has been investigated in stored manure. The manure collected from sulfadiazine ( 14 C-SDZ) and difloxacin ( 14 C-DIF) treated pigs contained N-acetylsulfadiazine (Ac-SDZ), 4-hydroxy-SDZ (4-OH-SDZ), and sarafloxacin (SARA) as the main metabolites, respectively along with their parent compounds. Manures were stored separately at 10 o C and 20 o C at various moisture levels. About 96-99% of the radioactivity remained in extractable parent compounds and their metabolites after 150 d of storage. The formation of non-extractable residue and the rate of mineralization were both negligible in manure containing SDZ and DIF. During storage SDZ concentration increased as a result of the deacetylation of Ac-SDZ, whose concentration decreased proportionally. Hence the environmental effects may be underestimated if the parent compound alone is considered for environmental risk assessment. About 11% and 14% of 4-OH-SDZ were lost after 20 and 40 d of storage; thereafter its concentration increased relatively, highlighting hydroxylation of SDZ. DIF degraded very slowly (7% loss after 150 d) during the storage of manure; in contrast the concentration of SARA decreased rapidly (72-90% loss after 150 d). Dilution of manure and storage at higher temperatures for a reasonable period of time enhanced the rate of reactions of SDZ, DIF and their related metabolites.

Analysis of PTA hardfacing with CoCrWC and CoCrMoSi alloys

Directory of Open Access Journals (Sweden)

Adriano Scheid

2013-12-01

Full Text Available CoCrWC alloys are widely used to protect components that operate under wear and high temperature environments. Enhanced performance has been achieved with the CoCrMoSi alloys but processing this alloy system is still a challenge due to the presence of the brittle Laves phase, particularly when welding is involved. This work evaluated Plasma Transferred Arc coatings processed with the Co-based alloy CoMoCrSi - Tribaloy T400, reinforced with Laves phase, comparing its weldability to the CoCrWC - Stellite 6, reinforced with carbides. Coatings were also analyzed regarding the response to temperature exposure at 600°C for 7 days and subsequent effect on microstructure and sliding abrasive wear. Coatings characterization was carried out by light and scanning electron microscopy, X-ray diffraction and Vickers hardness. CoCrWC coatings exhibited a Cobalt solid solution dendritic microstructure and a thin interdendritic region with eutectic carbides, while CoCrMoSi deposits exhibit a large lamellar eutectic region of Laves phase and Cobalt solid solution and a small fraction of primary Laves phase. Although phase stability was observed by X-ray diffraction, coarsening of the microstructure occurred for both alloys. CoCrMoSi showed thicker lamellar Laves phase and CoCrWC coarser eutectic carbides. Coatings stability assessed by wear tests revealed that although the wear rate of the as-deposited CoCrMoSi alloy was lower than that of CoCrWC alloy its increase after temperature exposure was more significant, 22% against 15%. Results were discussed regarding the protection of industrial components in particular, bearings in 55AlZn hot dip galvanizing components.

14C dating of early Neolithic settlement Galovo near Slavonski Brod in Northern Croatia

International Nuclear Information System (INIS)

Krajcar Bronic, I.; Minichreiter, K.

2007-01-01

In Northern Croatia, more than hundred settlements are known from the period of the Starcevo culture, the first Neolithic period in south-east (SE) Europe. Here we present the 14 C dating of nine charcoal samples from the Neolithic settlement Galovo in Slavonski Brod. According to archaeological findings, it belongs to the early phase (Linear A) of the Starcevo culture and has a special ritual-burial area separated by two wooden fences from its residential part. The vertical stratigraphy revealed two phases of the settlement construction in period 6070-5630 cal BC. In the younger phase (5380-4960 cal BC) the settlement expanded and the burial area became smaller. Combination of archaeological findings and 14 C dates thus allowed a reconstruction of the 1000-year-long existence of this settlement that existed simultaneously with the nearby settlement Zadubravlje-Duzine, dated earlier to 6000-5000 cal BC. These are the first absolute dates of the beginning of neolithization in Northern Croatia

Moessbauer spectroscopy characterization of Zr-Nb-Fe phases

Energy Technology Data Exchange (ETDEWEB)

Ramos, C.P. [CONICET, Av. Gral. Paz 1499, 1650 Buenos Aires (Argentina)]. E-mail: ciramos@cnea.gov.ar; Granovsky, M.S. [CAC-CNEA, Av. Gral. Paz 1499, 1650 Buenos Aires (Argentina); Saragovi, C. [CAC-CNEA, Av. Gral. Paz 1499, 1650 Buenos Aires (Argentina)

2007-02-01

The aim of this work was the characterization of the ternary phases and of those coming from the corresponding binary systems in the Zr-Nb-Fe diagram by means of Moessbauer spectroscopy. This is part of a complete study involving a tentative isothermal section at 900 deg. C of the center of the Zr-Nb-Fe diagram which will be published elsewhere. Zr-Nb-Fe alloys with Nb contents between 5 and 50 at% and Fe contents between 10 and 60 at% were analyzed after a heat treatment at 900 deg. C for 4 month. Moessbauer characterization of the phases was complemented by optical and scanning electron microscopies, X-ray diffraction and electron microprobe analysis. From the obtained results it can be inferred that Fe in both of the Laves phases present in this system (Zr(FeNb){sub 2} and (ZrNb)Fe{sub 2}) sees different environments, producing quadrupole splitting and hyperfine field distributions, respectively. Two types of body centered cubic {beta} phases (Zr-rich and Nb-rich) were found having noticeable differences in their Moessbauer parameters. Furthermore it was shown that the ternary Fe(NbZr){sub 2} compound would show magnetic character at low temperatures. Concentration dependence of the hyperfine parameters and their relations with the lattice parameters contributed to the structural characterization of the phases.

Moessbauer spectroscopy characterization of Zr-Nb-Fe phases

International Nuclear Information System (INIS)

Ramos, C.P.; Granovsky, M.S.; Saragovi, C.

2007-01-01

The aim of this work was the characterization of the ternary phases and of those coming from the corresponding binary systems in the Zr-Nb-Fe diagram by means of Moessbauer spectroscopy. This is part of a complete study involving a tentative isothermal section at 900 deg. C of the center of the Zr-Nb-Fe diagram which will be published elsewhere. Zr-Nb-Fe alloys with Nb contents between 5 and 50 at% and Fe contents between 10 and 60 at% were analyzed after a heat treatment at 900 deg. C for 4 month. Moessbauer characterization of the phases was complemented by optical and scanning electron microscopies, X-ray diffraction and electron microprobe analysis. From the obtained results it can be inferred that Fe in both of the Laves phases present in this system (Zr(FeNb) 2 and (ZrNb)Fe 2 ) sees different environments, producing quadrupole splitting and hyperfine field distributions, respectively. Two types of body centered cubic β phases (Zr-rich and Nb-rich) were found having noticeable differences in their Moessbauer parameters. Furthermore it was shown that the ternary Fe(NbZr) 2 compound would show magnetic character at low temperatures. Concentration dependence of the hyperfine parameters and their relations with the lattice parameters contributed to the structural characterization of the phases

Synthesis of [methyl-{sup 14}C]crotonobetaine from DL-[methyl-{sup 14}C]carnitine

Energy Technology Data Exchange (ETDEWEB)

Loester, H.; Seim, H. [Leipzig Univ. (Germany). Inst. of Clinical Chemistry and Pathobiochemistry

1996-02-01

The causes of carnitine deficiency syndromes are not completely understood, but decomposition of L-carnitine in vivo is likely to be involved. Carnitine is metabolized to {gamma}-butyrobetaine, and crotonobetaine is probably an intermediate in this pathway. To validate experimentally the precursor-product relationship between the three physiologically occuring {gamma}-betaines - L-carnitine, crotonobetaine, {gamma}-butyrobetaine - labelling with stable or radioactive isotopes became necessary. Methyl-labelled carnitine isomers (L(-)-, D(+)- or DL-) or {gamma}-butyrobetaine can be easily synthesized by methylation of 4-amino-3-hydroxybutyric acid isomers or 4-aminobutyric acid, respectively. Because of problems with the 4-aminocrotonic acid, we synthesized labelled crotonbetaine from labelled carnitine. Thus, DL-[methyl-{sup 14}C]carnitine was dehydrated by reaction with concentrated sulfuric acid. After removal of the latter the products were separated and purified by ion exchange chromatography on DOWEX 50 WX8 (200 - 400 mesh) and gradient elution with hydrochloric acid. In addition to the labelled main product [methyl-{sup 14}C]crotonobetaine (yield about 50 %), [methyl-{sup 14}C]glycine betaine and [methyl-{sup 14}C]acetonyl-trimethylammonium (ATMA) were formed. The end products were identified by combined thin layer chromatography/autoradiography and quantified by liquid scintillation counting. (Author).

14C concentrations in tree stems, 1

International Nuclear Information System (INIS)

Kikata, Yoji; Yonenobu, Hitoshi; Morishita, Fumio; Hattori, Yoshiaki; Marsoen, S.N.

1993-01-01

The 14 C concentrations in trees sampled at various latitudes were measured with a Tandetron Accelerator Mass Spectrometer at Nagoya University. The growing periods of the parts for 14 C measurements were estimated by the relationship between meteorological conditions and the appearance of anatomical features of annual rings such as false rings, latewood formation, and so on. The following results were obtained: 1. The latitude dependence of the 14 C variation is found in tree stems as well as in the atmosphere. 2. The 14 C concentrations in tree stems are almost equal to those in the atmosphere at the latitude where the tree had grown and at the time when the sampled section is formed. Therefore the 14 C concentrations in the atmosphere are estimated by those of the tree stems. 3. The time when the 14 C concentration in the tree showed its maximum value has difference of 1 - 2 years with that of the latitude where the tree had grown. 4. This phenomena seemed to be related closely with the mechanism of global mixing of 14 CO 2 produced by atmospheric nuclear weapon tests. This mechanism causes a time lag of 14 C variation between northern and southern hemisphere. (author)

Estimation of radiation dosage and transmutation effect of 14C involved in measuring rate of albumin synthesis with 14C-carbonate

International Nuclear Information System (INIS)

Yap, A.H.; Hafkenscheid, J.C.M.; Goossens, C.M.I.C.; Buys, W.C.A.M.; Binkhorst, R.A.; Van Tongeren, J.H.M.

1975-01-01

For direct measurement of the rate of albumin synthesis, Na 2 14 CO 3 was used intravenously. The assessment of the radiation hazard involved in the study was based on the knowledge of the minimum dose of Na 2 14 CO 3 necessary for a sufficient incorporation of 14 C in the guanidine-C of arginine in albumin to obtain measurable radioactivity. By measurement of expired 14 CO 2 and excreted 14 C-urea in the urine during a 5-hr period following intravenous administration of Na 2 14 CO 3 in five subjects, some quantitative data on 14 C retention and radiation dosage were obtained. In comparison with animal studies, the rate of expiration of 14 CO 2 in man is slower. About 50 percent of the total radioactivity injected was lost through the respiratory route in the first hour. The total amount of expired 14 C during the 5 hr of investigation was about 75 percent of the injected dose for the five subjects. The amount of 14 C excreted as urinary 14 C-urea during the 5 hr of investigation is very small in comparison with the expired 14 C; it was only about 0.5 percent of the dose injected. The total absorbed radiation dose after complete elimination of 14 C from the body was calculated with various assumptions. The extra risk of genetic damage due to disintegration of retained 14 C in comparison with that of natural 14 C in the body during 30 living years is about 50 percent. (U.S.)

Transfer of {sup 14}C to prenatal and neonatal rats from their mothers exposed to {sup 14}C compounds by ingestion

Energy Technology Data Exchange (ETDEWEB)

Takeda, H.; Fuma, S.; Miyamoto, K.; Kuroda, N.; Inaba, J

2003-07-01

The transfer of {sup 14}C through placenta or milk was investigated and the radiation dose to fetal and newborn rats was estimated. Female rats at gestational stages or after delivery were exposed to {sup 14}C in the form of sodium bicarbonate, thymidine and lysine by a single ingestion. Radioactivity in maternal tissues and conceptuses (placenta, fetal membrane and fetus) and in the newborn was determined at various times after ingestion. After exposure to these {sup 14}C compounds, there was no significant difference between the {sup 14}C concentration in the fetus and that in the maternal tissues, suggesting that the placenta has no effect in preventing or accelerating the placental transfer of {sup 14}C. The concentration and content of {sup 14}C in the fetus and newborn were, however, dependent on the chemical form of {sup 14}C and on the prenatal or neonatal stage at the time of ingestion. The result of the dose estimation showed that {sup 14}C-lysine gave significantly higher prenatal and neonatal doses than {sup 14}C-sodium bicarbonate or {sup 14}C-thymidine. (author)

Synthesis of [methyl-[sup 14]C]-N-methylputrescine

Energy Technology Data Exchange (ETDEWEB)

Secor, H.V.; Izac, R.R.; Hassam, S.B.; Frisch, A.F. (Philip Morris Research Center, Richmond, VA (United States))

1994-05-01

[Methyl-[sup 14]C]-N-methylputrescine was prepared from [[sup 14]C]methylamine hydrochloride in five steps. Reaction of benzaldehyde and [[sup 14]C]methylamine (10 mCi) followed by catalytic hydrogenation yielded [methyl-[sup 14]C]-N-methylbenzylamine. The key step in this process is the alkylation of [methyl-[sup 14]C]-N-methylbenzylamine in aqueous medium with 4-bromobutyronitrile. The radiochemical purity of the final product after two successive catalytic hydrogenations was in excess of 97%. The radiochemical yields in two successive runs were 26 and 38%, based on starting [[sup 14]C]methylamine, with specific activities of 22 and 23 mCi/mmol, respectively. This sequence provides a convenient and efficient regioselective radiosynthesis of [methyl-[sup 14]C]-N-methylputrescine. (author).

The precipitation response of 20%-cold-worked type 316 stainless steel to simulated fusion irradiation

International Nuclear Information System (INIS)

Maziasz, P.J.

1979-01-01

The precipitation response of 20%-cold-worked type 316 stainless steel has been examined after irradiation in HFIR at 380-600 0 C, after irradiation in EBR-II at 500 0 C, and after thermal aging at 600 to 750 0 C. Eta phase forms during exposure to all environments. It constitutes a major portion of the precipitation response, and is rich in Ni, Si and Mo relative to M 23 C 6 after thermal aging. It is not normally reported in 20%-cold-worked type 316 stainless steel. The eta, M 23 C 6 , Laves, sigma, and chi precipitate phases appear at similar temperatures after HFIR, EBR-II, or thermal exposure. There are, however, some differences in relative amounts, size, and distribution of phases among the various environments. Eta phase is the only carbide-type phase observed after irradiation in HFIR from 380-550 0 C. The large cavities associated with it at 380 0 C contribute significantly to swelling. Re-solution of fine M 23 C 6 , eta, and Laves particles and re-precipitation of massive particles of sigma, M 23 C 6 and chi are observed after recrystallization in HFIR. (orig.)

Effects of Pseudomonas species on the release of bound 14C residues from soil treated with [14C]atrazine

International Nuclear Information System (INIS)

Khan, S.U.; Behki, R.M.

1990-01-01

The release of bound (nonextractable) 14 C residues from soil previously treated with [ 14 C]atrazine was investigated by incubation of the solvent-extracted soil with two species of Pseudomonas capable of metabolizing atrazine. The two species, 192 and 194, released bound 14 C residues from the soil. Addition of glucose, known to increase microbiological activities, to the incubated soil appeared to enhance the release of soil-bound 14 C residues, in particular in the presence of Pseudomonas species 192. The 14 C bound residues in soil, mainly present as the parent compound and its hydroxy and monodealkylated analogues, were released into the incubation mixture and were subsequently metabolized by the two species involving dechlorination and dealkylation

Early incorporation and distribution of 14C-photosynthates after 14C-feeding for a brief period in tea plant

International Nuclear Information System (INIS)

Hakamata, Katsuhiro

1981-01-01

In order to clarify the early incorporation and distribution of 14 C-photosynthetic products in tea plants after 14 C-feeding for a brief period, 14 C-tracer experiments were performed, using the winter leaves, first crop shoots and young tea plants of a cultivar, Yabukita. As the results of the experiment on leaf disks by 14 C-Feeding for one minute, the 14 C-activity in the ethanol soluble fraction distributed in the anionic, cationic and neutral fractions in this order. When the time of feeding was extended to 10 min, the distribution in the cationic fraction decreased, and that in the neutral fraction increased. In the experiment on shoots, after the end of 10 min assimulation, the 14 C-activity in the ethanol soluble fraction distributed in the neutral, cationic and anionic fractions in this order. In course of time, the distribution in the cationic and anionic fractions decreased, and that in the neutral fraction increased. As the results of 14 C-feeding to young tea plants for 2.5 hours, 70 - 95% of the 14 C-activity in the ethanol soluble fraction distributed in the neutral fraction. Sucrose seemed to be the primary and early product of photosynthesis, and might be the principal carbohydrate form of translocation and reserve in tea plants. Raffinose and stachyose played almost the same role as sucrose. (Kako, I.)

Genetic consequences of the 14C-decay

International Nuclear Information System (INIS)

Gracheva, L.M.; Korolev, V.G.

1978-03-01

There are only few investigations on the biological and genetic consequences of 14 C decay especially due to the long half-life of 14 C. Naturally, the consequences of the decay of 14 C incorperated in DNA is of particular interest. Due to the thus occuring conversion into nitrogen, either opening of the ribose residue ring and base occurs or conversion into base analogue. The present work gives a survey on the investigational results on this topic which were obtained by various authors on phages, bacteria, algae and animal cells, as well as on molecular level. It was shown that the transmutation for the occurence of a lethal effect is many times more effective than β-radiation. Investigations of the mutagenic effects and other genetic effects of the 14 C decay were carried out on micro-organisms, however also on higher forms of life, plants, insects and mice. An analysis of the mutations showed that transitions as well as transversions occur. As example for genetic effects of 14 C decay, the two following are named. In the case of mice which were exposed to 14 CO 2 atmosphere, it was seen that the number of polyptoidal chromosome sets in the first spermotacytes increased considerably, an increase of the chromosome conversion rate was however not observed. When treating gryllus larvae with 14 C, it was interesting to note that the crossing of 14 C-contained females with normal males produced viable eggs, whereas normal females after crossing with 14 C contained males, laid no more eggs. (MG) 891 MG [de

Reviewing the Mid-First Millennium BC {sup 14}C 'warp' using {sup 14}C/bristlecone pine data

Energy Technology Data Exchange (ETDEWEB)

Taylor, R.E., E-mail: retaylor@ucr.edu [Department of Anthropology, University of California, Riverside, Riverside, CA (United States); Cotsen Institute of Archaeology, University of California, Los Angeles, CA (United States); Keck Carbon Cycle Accelerator Mass Spectrometry Laboratory, University of California, Irvine, CA (United States); Southon, John [Keck Carbon Cycle Accelerator Mass Spectrometry Laboratory, University of California, Irvine, CA (United States)

2013-01-15

AMS-based {sup 14}C measurements have been obtained on 53 dendrochronologically-dated Bristlecone pine (Pinus longaeva) wood samples in decadal increments spanning 2300-2750 cal BP with particular interest focused on the decades centered on 2405 cal BP and 2625 cal BP. In general, there is overall agreement with the current IntCal04/09 consensus calibration curve for this period. For the 2400-2410 cal BP interval, our Bristlecone-based {sup 14}C value is consistent with the {sup 14}C value obtained by Belfast on Irish oak for that decade but not on German oak values obtained by Seattle. Our {sup 14}C value for the 2620-2630 cal BP interval is consistent with the German oak (Heidelberg)-based {sup 14}C decadal value. The {sup 10}Be-based reconstruction of {sup 14}C variations over the 2620-2630 cal BP interval also supports the Heidelberg data although clearly additional clarifications are required before the current tree ring-based {sup 14}C and ice core-based {sup 10}Be data for this interval can be accurately interpreted and valid inferences obtained.

14C levels in Trombay environment

International Nuclear Information System (INIS)

Doshi, G.R.; Sadarangani, S.H.; Krishnamoorthy, T.M.

1994-01-01

The passive air sampling method has been used to measure the spatial distribution of the specific activity of 14 C in air samples collected within the Trombay complex. The samples collected within radial distance of about 0.5 km from Cirus showed 3 to 5 times higher specific activity of 14 C over the natural background level of 6.2 pCi/g C. The same decreased with the distance and approached the value of natural level at the site boundary (1.6 km). The specific activity of 14 C in leaf samples collected within the complex showed the similar pattern. (author). 6 refs., 2 tabs

[14C]Virginiamycin residues in eggs

International Nuclear Information System (INIS)

Corpet, D.E.; Baradat, M.; Bories, G.F.

1988-01-01

Laying hens were fed ab libitum a diet supplemented at 40, 10, and 0 mg/kg with [ 14 C]virginiamycin, to determine whether or not virginamycin or its metabolites were transferred to the eggs. About 0.05% of the ingested 14 C dose was recovered in the eggs. Radiolabeled residues expressed in terms of virginiamycin equivalents were found to be 5.1 ng/g in the albumen and 31.8 ng/g in the yolk from hens fed a 10 mg/kg diet. No antibiotic activity could be detected in the eggs. Tentative identifications showed that in the albumen about 17% of the 14 C behaved chromatographically like virginiamycin and 18% was associated to the ovalbumin. In the yolk 31% of the 14 C was associated to proteins, 58% to fatty acids, and 4% to unsaponifiable matter

Effect of homogenization heat treatments on the cast structure and tensile properties of nickel-base superalloy ATI 718Plus in the presence of boron and zirconium additions

Energy Technology Data Exchange (ETDEWEB)

Hosseini, Seyed Ali, E-mail: saliho3ini@gmail.com; Madar, Karim Zangeneh; Abbasi, Seyed Mehdi

2017-03-24

The effect of homogenization heat treatment on cast structure, hardness, and tensile properties of the nickel-based superalloy 718plus in the presence of boron and zirconium additives were investigated. For this purpose, five alloys with different contents of boron (0.00–0.016 wt%) and zirconium (0.0–0.1 wt%) were cast by double vacuum process VIM/VAR and then were homogenized at 1075–1175 °C for 5–25 h. Microstructural investigation by OM and SEM and phase analysis by XRD were done and then hardness and high temperature tensile tests were performed on the homogenized alloys. The results show that the amount of the Laves phase is reduced by increases in time and temperature of homogenization. It was also found that increases in duration of homogenization at 1075 °C results in improving strength and ductility, while duration increase at 1175 °C is accompanied with degradation of them, which caused the reduction of needle-like delta phase on grain boundaries. Boron and zirconium had negative effects on the strength and ductility of the alloy by increasing the amount of Laves in the cast structure. By increasing these elements in alloy composition, more time is needed in order to fully eliminate the Laves by homogenization treatment.

14C emission from Swedish nuclear power plants and its effect on the 14C levels in the environment

International Nuclear Information System (INIS)

Stenstroem, K.; Erlandsson, Bengt; Hellborg, R.; Kiisk, M.; Persson, Per; Mattsson, Soeren; Thornberg, C.; Skog, G.

2000-02-01

The radionuclide 14 C is produced in all types of nuclear reactors mainly by neutron induced reactions in oxygen ( 17 O), nitrogen ( 14 N) and carbon ( 13 C). Part of the 14 C created is continuously released during normal operation as airborne effluents in various chemical forms (such as CO 2 , CO and hydrocarbons) to the surroundings. Because of the biological importance of carbon and the long physical half-life of 14 C, it is of interest to measure the releases and their incorporation into living material. The 14 C activity concentrations in annual tree rings and air around two Swedish nuclear power plants (Barsebaeck and Forsmark) as well as the background 14 C activity levels from two reference sites in southern Sweden during 1973-1996 are presented in this report. In order to verify the reliability of the method some investigations have been conducted at two foreign nuclear sites, Sellafield fuel reprocessing plant in England, and Pickering nuclear generating station in Canada, where the releases of 14 C are known to be substantial. Furthermore, results from some measurements in the vicinity of Paldiski submarine training centre in Estonia are presented. The results of the 14 C measurements of air, vegetation and annual tree rings around the two Swedish nuclear power plants show very low enhancements of 14 C, if at all above the uncertainty of the measurements. Even if the accuracy of the measurements of the annual tree rings is rather good (1-2%) the contribution of 14 C from the reactors to the environment is so small that it is difficult to separate it from the prevailing background levels of 14 C . This is the case for all sampling procedures: in air and vegetation as well as in annual tree rings. Only on a few occasions an actual increase is observed. However, although the calculations suffer from rather large uncertainties, the calculated release rate from Barsebaeck is in fair agreement with reported release data. The results of this investigation show

ORIGIN OF PALMITIC ACID CARBON IN PALMITATES FORMED FROM HEXADECANE-1-C14 AND TETRADECANE-1-C14 BY MICROCOCCUS CERIFICANS

Science.gov (United States)

Finnerty, W. R.; Kallio, R. E.

1964-01-01

Finnerty, W. R. (University of Iowa, Iowa City), and R. E. Kallio. Origin of palmitic acid carbon in palmitates formed from hexadecane-1-C14 and tetradecane-1-C14 by Micrococcus cerificans. J. Bacteriol. 87:1261–1265. 1964.—Degradation of the palmitic acid moiety of cetyl palmitate and myristyl palmitate formed from hexadecane-1-C14 and tetradecane-1-C14 by Micrococcus cerificans was carried out. The patterns of C14 labeling in palmitic acid from cetyl palmitate showed that hexadecane is oxidized at the C1 position, and cetyl alcohol and palmitic acid thus formed are directly esterified. Palmitic acid arising from tetradecane and esterified to tetradecanol appeared to have been synthesized by the addition of two carbon atoms to an existing 14-carbon atom skeleton. Considerable mixing of C14 occurred in the C1 and C2 positions of palmitic acid thus synthesized. PMID:14188700

Analysis of 14C and 13C in teeth provides precise birth dating and clues to geographical origin.

Science.gov (United States)

Alkass, K; Buchholz, B A; Druid, H; Spalding, K L

2011-06-15

The identification of human bodies in situations when there are no clues as to the person's identity from circumstantial data, poses a difficult problem to the investigators. The determination of age and sex of the body can be crucial in order to limit the search to individuals that are a possible match. We analyzed the proportion of bomb pulse derived carbon-14 ((14)C) incorporated in the enamel of teeth from individuals from different geographical locations. The 'bomb pulse' refers to a significant increase in (14)C levels in the atmosphere caused by above ground test detonations of nuclear weapons during the cold war (1955-1963). By comparing (14)C levels in enamel with (14)C atmospheric levels systematically recorded over time, high precision birth dating of modern biological material is possible. Above ground nuclear bomb testing was largely restricted to a couple of locations in the northern hemisphere, producing differences in atmospheric (14)C levels at various geographical regions, particularly in the early phase. Therefore, we examined the precision of (14)C birth dating of enamel as a function of time of formation and geographical location. We also investigated the use of the stable isotope (13)C as an indicator of geographical origin of an individual. Dental enamel was isolated from 95 teeth extracted from 84 individuals to study the precision of the (14)C method along the bomb spike. For teeth formed before 1955 (N=17), all but one tooth showed negative Δ(14)C values. Analysis of enamel from teeth formed during the rising part of the bomb-spike (1955-1963, N=12) and after the peak (>1963, N=66) resulted in an average absolute date of birth estimation error of 1.9±1.4 and 1.3±1.0 years, respectively. Geographical location of an individual had no adverse effect on the precision of year of birth estimation using radiocarbon dating. In 46 teeth, measurement of (13)C was also performed. Scandinavian teeth showed a substantially greater depression in

Synthesis of 1-(4-methylsulfone-phenyl)-5-(4-fluoro-phenyl)-5-[14C]-1,2,3- triazole and 1-(4-sulfonamide-phenyl)-5-(4-fluoro-phenyl)-5-[14C]-1,2,3- triazole as novel carbon-14 anticonvulsant

International Nuclear Information System (INIS)

Saemian, N.; Shirvani, G.; Matloubi, H.

2006-01-01

Two 1,2,3-triazole anticonvulsants, 1-(4-methylsulfone-phenyl)-5-(4-fluoro-phenyl)-5-[ 14 C]-1,2,3-triazole and 1-(4-sulfonamide-phenyl)-5-(4- fluoro-phenyl)-5-[ 14 C]-1,2,3-triazole, both labeled with carbon-14 in the 5-position were prepared from para-fluoro-benzonitrile-[cyano- 14 C]. (author)

Degradation of 14C-parathion 'in vitro' by microorganisms isolated from a gley humic soil

International Nuclear Information System (INIS)

Andrea, M.M. de; Ruegg, E.F.

1982-01-01

It was determined 'in vitro' the degradation of Parathion by a bacterium and a fungus isolated from a sample of Gley Humic soil previously treated with repeated applications of the insecticide. In a qualitative colorimetric assay hydrolisis of parathion to p-nitrophenol just the bacterium gave a positive answer. In quantitative assays of 14 C-parathion degradation in culture media containing both microorganisms, organic solvents extractions resulted in organic and aqueous phases, which were analysed by liquid scintillation counting and thin-layer chromatography. In a mineral salts medium plus buffer, the bacterium and the fungus behaved differently from the control, because part of the 14 C-insecticide was metabolized to, at least, one metabolite and besides, the microorganisms presented smaller percentages of total recovery. The largest percentage of the radio carbon recovery from the extracts of the medium containing the fungus plus extract of yeast, was obtained from the aqueous phase and the existence of other metabolite was demonstrated by chromatograms of the organic phase. (Author) [pt

Dicty_cDB: FC-BS14 [Dicty_cDB

Lifescience Database Archive (English)

Full Text Available FC (Link to library) FC-BS14 (Link to dictyBase) - - - Contig-U16399-1 FC-BS14E (Li...nk to Original site) - - - - - - FC-BS14E 534 Show FC-BS14 Library FC (Link to library) Clone ID FC-BS14 (Li.../dictycdb.biol.tsukuba.ac.jp/CSM/FC/FC-BS/FC-BS14Q.Seq.d/ Representative seq. ID FC-BS...14E (Link to Original site) Representative DNA sequence >FC-BS14 (FC-BS14Q) /CSM/FC/FC-BS/FC-BS14Q.Seq.... vs CSM-cDNA Score E Sequences producing significant alignments: (bits) Value FC-BS14 (FC-BS

Intermetallic Strengthened Alumina-Forming Austenitic Steels for Energy Applications

Energy Technology Data Exchange (ETDEWEB)

Hu, Bin [Dartmouth College, Hanover, NH (United States); Baker, Ian [Dartmouth College, Hanover, NH (United States)

2016-03-31

In order to achieve energy conversion efficiencies of >50 % for steam turbines/boilers in power generation systems, the materials required must be strong, corrosion-resistant at high temperatures (>700°C), and economically viable. Austenitic steels strengthened with Laves phase and L1₂ precipitates, and alloyed with aluminum to improve oxidation resistance, are potential candidate materials for these applications. The creep resistance of these alloys is significantly improved through intermetallic strengthening (Laves-Fe₂Nb + L1₂-Ni₃Al precipitates) without harmful effects on oxidation resistance. Microstructural and microchemical analyses of the recently developed alumina-forming austenitic (AFA) steels (Fe-14Cr-32Ni-3Nb-3Al-2Ti-based) indicated they are strengthened by Ni₃Al(Ti) L1₂, NiAl B₂, Fe₂Nb Laves phase and MC carbide precipitates. Different thermomechanical treatments (TMTs) were performed on these stainless steels in an attempt to further improve their mechanical properties. The thermo-mechanical processing produced nanocrystalline grains in AFA alloys and dramatically increased their yield strength at room temperature. Unfortunately, the TMTs didn’t increase the yield strengths of AFA alloys at ≥700ºC. At these temperatures, dislocation climb is the dominant mechanism for deformation of TMT alloys according to strain rate jump tests. After the characterization of aged AFA alloys, we found that the largest strengthening effect from L1₂ precipitates can be obtained by aging for less than 24 h. The coarsening behavior of the L1₂ precipitates was not influenced by carbon and boron additions. Failure analysis and post-mortem TEM analysis were performed to study the creep failure mechanisms of these AFA steels after creep tests. Though the Laves and B2-NiAl phase precipitated along the boundaries can improve the creep properties, cracks were

Excitation functions of the systems 12C+14C and 13C+12C

International Nuclear Information System (INIS)

Haindl, E.

1975-01-01

The excitation functions of the systems 12 C+ 14 C and 13 C+ 12 C are investigated for different exit channels. The excitation functions measured do not show correlated structures as in the system 12 C+ 12 C. (WL/AK) [de

Determination of 14CO2 in breath and 14C in stool after oral administration of cholyl-1-[14C]glycine: clinical application

International Nuclear Information System (INIS)

Roda, A.; Roda, E.; Aldini, R.; Mazzella, G.; Festi, D.; Sama, C.; Barbara, L.

1977-01-01

Twenty patients with intestinal bacterial overgrowth and 20 control subjects were investigated for bile acid deconjugation, by measuring 14 CO 2 in the breath after cholyl-1-[ 14 C]glycine administration. 14 CO 2 output/24 h was 11.0 +- 5.2% (mean +- SD) in controls and 54.2 +- 14.0% (mean +- SD) in bacterial-overgrowth patients (P 14 CO 2 excretion rate in 12 h, when normalized to 100% of the dose at the 12th hour, gave an even finer discrimination between the two groups (no false responses). 14 C in stool, analyzed in 20 malabsorption patients and 20 controls by two different techniques, was 6.6 +- 4% and 31.38 +- 20.7% (mean +- SD), respectively. Results by the two different techniques described here correlated well (r = 0.99). Bile acid malabsorption was in reasonable agreement (r = 0.67) with percentage of ''chenoid'' (chenodeoxycholic acid plus ursodeoxycholic acid) in the stool by gas-liquid chromatography; a poorer correlation was observed when ''choloid'' (cholic acid plus its epimers) were plotted vs. 14 C in stool

The production of (14C) oxalate during the metabolism of (14C) carbohydrates in isolated rat hepatocytes.

Science.gov (United States)

Rofe, A M; James, H M; Bais, R; Edwards, J B; Conyers, R A

1980-04-01

Oxalate (14C) was produced during the metabolism of (U-14C) carbohydrates in hepatocytes isolated from normal rats. At 10 mM, the order of oxalate production was fructose > glycerol > xylitol > sorbitol greater than or equal to glucose in the ratio 10 : 4 : 3 : 1 : 1. This difference between oxalate production from fructose and glucose was reflected in their rates of utilisation, glucose being poorly metabolised in hepatocytes from fasted rats. Fructose was rapidly metabolised, producing glucose, lactate and pyruvate as the major metabolites. Glycerol, xylitol and sorbitol were metabolised at half the rate of fructose, the major metabolites being glucose, lactate and glycerophosphate. The marked similarity in the pattern of intermediary metabolites produced by these polyols was not, however, reflected in the rates of oxalate production. Hepatic polyol metabolism resulted in high levels of cytosolic NADH, as indicated by elevated lactate : pyruvate and glycerophosphate : dihydroxyacetone phosphate ratios. The artificial electron acceptor, phenazine methosulphate (PMS) stimulated oxalate production from the polyols, particularly xylitol. In the presence of PMS, the order of oxalate production was fructose greater than or equal to xylitol > glycerol > sorbitol in the ratio 10 : 10 : 6 : 2. The production of glucose, lactate and pyruvate from the polyols was also stimulated by PMS, whereas the general metabolism of fructose, including oxalate production, was little affected. Oxalate (14C) was produced from (1-14C), (2-14C) and (6-14C) but not (3,4-14C) glucose in hepatocytes isolated from non-fasted, pyridoxine-deficient rats. Whilst this labelling pattern is consistent with oxalate being produced by a number of pathways, it is suggested that metabolism via hydroxypyruvate is a major route for oxalate production from various carbohydrates, with perhaps the exception of xylitol, which appears to have an alternative mechanism for oxalate production. The observation that

Incorporation of 14C-succinate in Synechococcus

International Nuclear Information System (INIS)

Doehler, G.

1983-01-01

The cyanobacterium Synechococcus (= Anacystis nidulans) was grown under normal air conditions (0.03 vol.% CO 2 ) and in low white light (0.5 x 10 3 μW/cm 2 ) at 37 0 C. Kinetics of 14 C incorporation into several soluble products and pigments were studied after adding 14 C-succinate during photosynthesis and in the dark using the autoradiographic method. Radioactivity was found mainly in glutamate and aspartate during the photosynthetic period independent on 3-(3',4'-dichlorphenyl)-1,1-dimethylurea preincubation. In the dark period 14 C label could also be detected in malate. Short-term kinetics experiments showed a decrease in 14 C label of glutamate and a parallel increase of aspartate. Results were discussed in respect to the interrupted tricarboxylic acid cycle. (author)

Reactions of saccharides catalyzed by molybdate ions. XXXIII. Use of. cap alpha. (U-/sup 14/C)glucan for preparation of /sup 14/C-labelled saccharides

Energy Technology Data Exchange (ETDEWEB)

Bilik, V; Biely, P [Institute of Chemistry, Centre for Chemical Research, Slovak Academy of Sciences, Bratislava (Czechoslovakia); Kolina, J [Ustav pro Vyzkum, Vyrobu a Vyuziti Radioisotopu, Prague (Czechoslovakia)

1984-01-01

D-(U-/sup 14/C)glucose obtained in acid hydrolysis of ..cap alpha..-(U-/sup 14/C)glucan (2 M-HCl) was epimerized under a catalytic action of molybdate ions to D-(U-/sup 14/C)mannose isolated with a 20% yield. Oxidative degradation of 4-nitrophenylhydrazones of D-(U-/sup 14/C)arabinose and D-(U-/sup 14/C)xylose resulted in D-(U-/sup 14/C)erythrose and D-(U-/sup 14/C)threose, respectively, with a 15% yield relative to the starting aldopentoses. Nitromethane synthesis with D-(U-/sup 14/C)lyxose followed by oxidative decomposition of the corresponding nitrohexitols yielded /sup 14/C-labelled D-galactose. Described is also the preparation of D-(U-/sup 14/C)arabinose from D-(U-/sup 14/C)glucose and the conversion of D-(U-/sup 14/C)arabinose to D-(U-/sup 14/C)xylose and D-(U-/sup 14/C)lyxose.

14C Behaviour in PWR coolant

International Nuclear Information System (INIS)

Sims, Howard; Dickinson Shirley; Garbett, Keith

2012-09-01

Although 14 C is produced in relatively small amounts in PWR coolant, it is important to know its fate, for example whether it is released by gaseous discharge, removed by absorption on ion exchange (IX) resins or deposited on the fuel pin surfaces. 14 C can exist in a range of possible chemical forms: inorganic carbon compounds (probably mainly CO 2 ), elemental carbon, and organic compounds such as hydrocarbons. This paper presents results from a preliminary survey of the possible reactions of 14 C in PWR coolant. The main conclusions of the study are: - A combination of thermal and radiolytic reactions controls the chemistry of 14 C in reactor coolant. A simple chemical kinetic model predicts that CH 3 OH would be the initial product from radiolytic reactions of 14 C following its formation from 17 O. CH 3 OH is predicted to arise as a result of reactions of OH . with CH 4 and CH 3 , and it persists because there is no known radiation chemical reduction mechanism. - Thermodynamic considerations show that CH 3 OH can be thermally reduced to CH 4 in PWR conditions, although formation of CO 2 from small organics is the most thermodynamically favourable outcome. Such reactions could be catalysed on active nickel surfaces in the primary circuit. - Limited plant data would suggest that CH 4 is the dominant form in PWR and CO 2 in BWR. This implies that radiation chemistry may be important in determining the speciation. - Addition of acetate does not affect the amount of 14 C formed, but the addition of large amounts of stable carbon would lead to a large range of additional products, some of which would be expected to deposit on fuel pin surfaces as high molecular weight hydrocarbons. However, the subsequent thermal decomposition reactions of these products are not known. - Acetate addition may represent a small input of 12 C compared with organic material released from CVCS resins, although the importance of this may depend on whether that is predominantly soluble

Synthesis of (/sup 14/C)Zolpidem

Energy Technology Data Exchange (ETDEWEB)

Allen, J.; Tizot, A.

1986-04-01

The synthesis of (/sup 14/C)Zolpidem, a new hypnotic agent having a non-benzodiazepine structure, is described. This compound was synthesised in a 64% overall radiochemical yield from potassium (/sup 14/C)cyanide and with a specific radioactivity of 56 mCi/mmol. It was used for pharmacokinetic and drug metabolism studies.

Fate and persistence of 14C pesticide residues in different soils: effects of 14C pesticide contaminated run-off soil water on biological systems. Part of a coordinated programme on isotopic-tracer-aided studies of agrochemical residue - soil biota interactions

International Nuclear Information System (INIS)

Lichtenstein, E.

1982-09-01

The interaction of selected fungicides, herbicides and N-fertilizers with microorganisms in cranberry soils and their effects on the degradation of 14 C-phenyl-parathion were investigated. Incubation of soils with parathion of p-nitrophenol for 4 days, followed by the addition of 14 C-parathion resulted after 24 h in an enhanced degradation of the insecticide to 14 CO 2 (34-39% of the applied radiocarbon as opposed to 2% in controls) and also in an increased binding of 14 C to the soil. The fungicide captafol inhibited the degradation of soil-applied 14 C-parathion as evidenced by a reduction of both 14 CO 2 evolution and 14 C-bound residues. Maneb and benomyl suppressed the degradation of 14 C-parathion to 14 CO 2 but not the formation of bound residues. Addition of 2,4-D to 14 C-parathion treated soil also resulted in an increased persistence of the insecticide. Studies conducted with the insecticide and (NH 4 ) 2 SO 4 , NH 4 NO 3 , KNO 3 or urea showed that under all experimental conditions the total amounts of 14 C recovered were similar, yet the distribution of 14 C-compounds into benzene-soluble, water-soluble and bound residues was not. This possibly indicated a change in the pathway of 14 C-parathion degradation. The insecticide was most persistent in soils containing (NH 4 ) 2 SO 4 , as demonstrated by a recovery of 29% of the applied radiocarbon in benzene-soluble form. Analyses by TIC of this benzene extraction phase revealed the presence of 14 C-parathion, 14 C-p-aminophenol and 14 C-aminoparathion

Transformation of the herbicide [14C]glufosinate in soils

International Nuclear Information System (INIS)

Smith, A.E.

1989-01-01

The degradation of 2 μg/g [ 14 C]glufosinate (DL-homoalan-4-ylmethylphosphinic acid) was studied in clay, clay loam, and sandy loam soils at 85% field capacity and at 20 degree C. Over a 4-week period the soils were extracted and analyzed for transformation products by radiochemical and gas chromatographic techniques. In all soils there was release of [ 14 C]carbon dioxide and formation of [ 14 C]-3-(hydroxymethylphosphinyl)propionic acid (MPPA) as major degradation products. Within 21 days, about 55% of the applied 14 C herbicide had been transformed to MPPA in the sandy loam and 19% to [ 14 C]carbon dioxide. After 28 days, approximately 45% of the 14 C herbicide had been transformed to MPPA in the clay and clay loam and 10% released as [ 14 C]carbon dioxide. At all samplings, other 14 C transformation products appeared to be insignificant

Accelerator mass spectrometry analysis of 14C-oxaliplatin concentrations in biological samples and 14C contents in biological samples and antineoplastic agents

Science.gov (United States)

Toyoguchi, Teiko; Kobayashi, Takeshi; Konno, Noboru; Shiraishi, Tadashi; Kato, Kazuhiro; Tokanai, Fuyuki

2015-10-01

Accelerator mass spectrometry (AMS) is expected to play an important role in microdose trials. In this study, we measured the 14C concentration in 14C-oxaliplatin-spiked serum, urine and supernatant of fecal homogenate samples in our Yamagata University (YU) - AMS system. The calibration curves of 14C concentration in serum, urine and supernatant of fecal homogenate were linear (the correlation coefficients were ⩾0.9893), and the precision and accuracy was within the acceptance criteria. To examine a 14C content of water in three vacuum blood collection tubes and a syringe were measured. 14C was not detected from water in these devices. The mean 14C content in urine samples of 6 healthy Japanese volunteers was 0.144 dpm/mL, and the intra-day fluctuation of 14C content in urine from a volunteer was little. The antineoplastic agents are administered to the patients in combination. Then, 14C contents of the antineoplastic agents were quantitated. 14C contents were different among 10 antineoplastic agents; 14C contents of paclitaxel injection and docetaxel hydrate injection were higher than those of the other injections. These results indicate that our quantitation method using YU-AMS system is suited for microdosing studies and that measurement of baseline and co-administered drugs might be necessary for the studies in low concentrations.

Appraisal of the /sup 14/C-glycocholate acid test with special reference to the measurement of faecal /sup 14/C excretion

Energy Technology Data Exchange (ETDEWEB)

Scarpello, J H.B.; Sladen, G E [Royal Hospital, Sheffield (UK). Academic Div. of Medicine

1977-09-01

The /sup 14/C-glycocholate test, including the measurement of marker corrected faecal /sup 14/C, has been assessed in the following groups of subjects: normal controls (18), patients with diarrhoea not attributable to altered bile acid metabolism (21), patients with diverticula of the small intestine (12), patients with previous resection of ileum and often proximal colon (34), and established ileostomists (10). Patients with diverticular disease had increased breath /sup 14/CO/sub 2/ excretion, but normal faecal excretion of /sup 14/C, and this test was more frequently abnormal than the Schilling test. Ileostomists excreted increased amounts of faecal /sup 14/C, even when the ileum was intact and apparently normal. The pattern after resection was complex. Breath /sup 14/C output was normal if the ileal resection was less than 25 cm in length, although some of these patients had increased faecal /sup 14/C excretion if, in addition, at least 15 cm of proximal colon had been resected or by-passed. Longer ileal resections were associated with increased breath and/or faecal /sup 14/C excretion, depending in part on the length of colon resected or by-passed and the 24 hour faecal volume. Fewer than half these patients had both increased breath and faecal excretion of isotope and faecal /sup 14/C alone was occasionally normal with an ileal resection of 50 cm or more. The /sup 14/C-glycocholate test was more frequently abnormal than the Schilling test in this group. The use of faecal marker correction had only a minor impact on the results. These data suggest that, in patients with ileal resection, faecal /sup 14/C, like faecal weight, is determined by the extent of colonic resection as well as by the amount of ileum resected.

Scenarios for 14C release to the atmosphere by the world nuclear industry and estimated radiological impacts

International Nuclear Information System (INIS)

Till, J.E.; Killough, G.G.

1978-01-01

This paper presents an assessment of the radiation dose to the world population and the associated potential health effects from three scenarios of 14 C releases by the nuclear industry between 1975 and 2020. Measures of health impact are derived from source terms through the use of a multicompartment model of the global carbon cycle, dose-rate factors based on 14 C specific activity in various organs of man, and health-effect incidence factors recently recommended by the International Commission on Radiological Protection. The scenarios for worldwide 14 C releases considered are (1) a pessimistic scenario in which all the 14 C projected to be produced in fuel cycles is released, (2) an optimistic scenario that assumes a decontamination factor of 100 for fuel reprocessing, and (3) an intermediate scenario that simulates a phased improvement in effluent treatment technology at reprocessing plants. The estimates of cumulative potential health effects are based on integrations over infinite time. Comparisons with estimated effects from naturally formed 14 C are shown

Prevalence of antibodies to prothrombin in solid phase (aPT) and to phosphatidylserine-prothrombin complex (aPS/PT) in patients with and without lupus anticoagulant.

Science.gov (United States)

Bertolaccini, Maria Laura; Sciascia, Savino; Murru, Veronica; Garcia-Fernandez, Cesar; Sanna, Giovanni; Khamashta, Munther A

2013-02-01

Antibodies to prothrombin in solid phase (aPT) and those to phosphatidiyserine-prothrombin complex (aPS/PT) have been suggested to strongly correlate with the presence of lupus anticoagulant (LA). As their clinical diagnostic value and true relationship with the LA remains elusive, we designed this study to evaluate the prevalence and significance of aPT and aPS/PT in a large cohort of patients with and without LA. Samples from 257 patients were included. aPT and aPS/PT were tested by ELISA. LA was tested as per the current criteria from the ISTH Subcommittee on LA-Phospholipid-dependent antibodies. aPS/PT and aPT were found in 51% and 32% of LA-positive (LA+ve) patients and in 22% and 28% of LA-negative (LA-ve) patients, respectively. Thrombosis, particularly venous thrombosis was associated with IgG aPT in the LA+ve group (p=0.0006) and in the LA-ve group (p=0.017). Antibodies to phosphatidylserine-prothrombin, either IgG and IgM were associated with thrombosis in general (p=0.0003) in particularly with venous thrombosis in the LA+ve group (paPS/PT were independent risk factors for thrombosis and pregnancy loss. In conclusion, aPS/PT, but not aPT, are more frequently found in patients with LA. Their association with thrombosis seems to be independent of the presence of LA.

Role of biotransformation, sorption and mineralization of "1"4C-labelled sulfamethoxazole under different redox conditions

International Nuclear Information System (INIS)

Alvarino, T.; Nastold, P.; Suarez, S.; Omil, F.; Corvini, P.F.X.; Bouju, H.

2016-01-01

"1"4C-sulfamethoxazole biotransformation, sorption and mineralization was studied with heterotrophic and autotrophic biomass under aerobic and anoxic conditions, as well as with anaerobic biomass. The "1"4C-radiolabelled residues distribution in the solid, liquid and gas phases was closely monitored along a total incubation time of 190 h. Biotransformation was the main removal mechanism, mineralization and sorption remaining below 5% in all the cases, although the presence of a carbon source exerted a positive effect on the mineralization rate by the aerobic heterotrophic bacteria. In fact, an influence of the type of primary substrate and the redox potential was observed in all cases on the biotransformation and mineralization rates, since an enhancement of the removal rate was observed when an external carbon source was used as a primary substrate under aerobic conditions, while a negligible effect was observed under nitrifying conditions. In the liquid phases collected from all assays, up to three additional peaks corresponding to "1"4C-radiolabelled residues were detected. The highest concentration was observed under anaerobic conditions, where two radioactive metabolites were detected representing each around 15% of the total applied radioactivity after 180 h incubation. One of the metabolites detected under anoxic and anaerobic conditions, is probably resulting from ring cleavage of the isoxazole ring. - Highlights: • New procedure based on "1"4C to determine sulfamethoxazole (SMX) removal • Complete SMX mass balances in solid, liquid and gas phases • Quantification of SMX biotransformation, mineralization and sorption • Influence of the primary metabolism and redox potential on SMX removal • SMX metabolites have been detected and a possible chemical structure was proposed.

Role of biotransformation, sorption and mineralization of {sup 14}C-labelled sulfamethoxazole under different redox conditions

Energy Technology Data Exchange (ETDEWEB)

Alvarino, T., E-mail: teresa.alvarino@usc.es [Department of Chemical Engineering, Institute of Technology, University of Santiago de Compostela, E-15782 Santiago de Compostela (Spain); Nastold, P. [Institute for Ecopreneurship, School of Life Sciences, University of Applied Sciences Northwestern Switzerland, 40 Grundenstrasse, CH 4132 Muttenz (Switzerland); Suarez, S.; Omil, F. [Department of Chemical Engineering, Institute of Technology, University of Santiago de Compostela, E-15782 Santiago de Compostela (Spain); Corvini, P.F.X. [Institute for Ecopreneurship, School of Life Sciences, University of Applied Sciences Northwestern Switzerland, 40 Grundenstrasse, CH 4132 Muttenz (Switzerland); State Key Laboratory for Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210093 (China); Bouju, H. [Institute for Ecopreneurship, School of Life Sciences, University of Applied Sciences Northwestern Switzerland, 40 Grundenstrasse, CH 4132 Muttenz (Switzerland)

2016-01-15

{sup 14}C-sulfamethoxazole biotransformation, sorption and mineralization was studied with heterotrophic and autotrophic biomass under aerobic and anoxic conditions, as well as with anaerobic biomass. The {sup 14}C-radiolabelled residues distribution in the solid, liquid and gas phases was closely monitored along a total incubation time of 190 h. Biotransformation was the main removal mechanism, mineralization and sorption remaining below 5% in all the cases, although the presence of a carbon source exerted a positive effect on the mineralization rate by the aerobic heterotrophic bacteria. In fact, an influence of the type of primary substrate and the redox potential was observed in all cases on the biotransformation and mineralization rates, since an enhancement of the removal rate was observed when an external carbon source was used as a primary substrate under aerobic conditions, while a negligible effect was observed under nitrifying conditions. In the liquid phases collected from all assays, up to three additional peaks corresponding to {sup 14}C-radiolabelled residues were detected. The highest concentration was observed under anaerobic conditions, where two radioactive metabolites were detected representing each around 15% of the total applied radioactivity after 180 h incubation. One of the metabolites detected under anoxic and anaerobic conditions, is probably resulting from ring cleavage of the isoxazole ring. - Highlights: • New procedure based on {sup 14}C to determine sulfamethoxazole (SMX) removal • Complete SMX mass balances in solid, liquid and gas phases • Quantification of SMX biotransformation, mineralization and sorption • Influence of the primary metabolism and redox potential on SMX removal • SMX metabolites have been detected and a possible chemical structure was proposed.

Synthesis of (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)olivetolic acid, methyl (1'-/sup 13/C)olivetolate and (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)cannabigerolic acid

Energy Technology Data Exchange (ETDEWEB)

Porwoll, J P; Leete, E [Minnesota Univ., Minneapolis (USA). Dept. of Chemistry

1985-03-01

Potential advanced intermediates in the biosynthesis of delta/sup 9/-tetrahydrocannabinol, the major psychoactive principle of marijuana, have been synthesized labeled with two contiguous /sup 13/C atoms and /sup 14/C. Methyl (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)olivetolate was prepared from lithium (/sup 13/C/sub 2/)acetylide and dimethyl (2-/sup 14/C)malonate. Reaction with geranyl bromide afforded methyl (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)cannabigerolate, and hydrolysis of these methyl esters with lithium propyl mercaptide yielded the corresponding labeled acids. The /sup 13/C-/sup 13/C couplings observable in the /sup 13/C NMR spectra of these /sup 13/C-enriched compounds and their synthetic precursors are recorded. Methyl (1'-/sup 14/C)olivetolate was prepared from /sup 13/CO/sub 2/ to confirm assignments of the /sup 13/C chemical shifts in the pentyl side chain of these compounds.

Impact of off-diagonal cross-shell interaction on 14C

Science.gov (United States)

Yuan, Cen-Xi

2017-10-01

A shell-model investigation is performed to show the impact on the structure of 14C from the off-diagonal cross-shell interaction, 〈pp|V|sdsd〉, which represents the mixing between the 0 and 2ħω configurations in the psd model space. The observed levels of the positive states in 14C can be nicely described in 0-4ħω or a larger model space through the well defined Hamiltonians, YSOX and WBP, with a reduction of the strength of the 〈pp|V|sdsd〉 interaction in the latter. The observed B(GT) values for 14C can be generally described by YSOX, while WBP and their modifications of the 〈pp|V|sdsd〉 interaction fail for some values. Further investigation shows the effect of such interactions on the configuration mixing and occupancy. The present work shows examples of how the off-diagonal cross-shell interaction strongly drives the nuclear structure. Supported by National Natural Science Foundation of China (11305272), Special Program for Applied Research on Super Computation of the NSFC Guangdong Joint Fund (the second phase), the Guangdong Natural Science Foundation (2014A030313217), the Pearl River S&T Nova Program of Guangzhou (201506010060), the Tip-top Scientific and Technical Innovative Youth Talents of Guangdong special support program (2016TQ03N575), and the Fundamental Research Funds for the Central Universities (17lgzd34)

European dendrochronoloy and C-14 dating of timber

International Nuclear Information System (INIS)

Fletcher, J.M.

1975-01-01

An account is given of the development of dendrochronology and C-14 dating in Europe. Corrections to raw C-14 dates, sampling and the uncertainty of C-14 ages of wood, and correlation of dates obtained by the two methods, are discussed. (U.K.)

Phase diagrams for pseudo-binary carbide systems TiC-NbC, TiC-TaC, ZrC-NbC, ZrC-TaC and HfC-TaC

International Nuclear Information System (INIS)

Gusev, A.I.

1985-01-01

Parameters of interaction and energy of mutual exchange in the liquid and solid phases of pseudobinary TiC-NbC, TiC-TaC, ZrC-NbC, ZrC-TaC, HfC-TaC systems are calculated with account of dependence on composition and temperature. Positions of liquidus-solidus phase boundaries on the phase diagrams of the mentioned systems are calculated on the basis of the determined mutual exchange energies in approximati.on of subregular solutions. The existance of latent decomposition ranges in the solid phase on the phase diagrams of the investgated systems is established

Synthesis of 14C-labeled stepholidine

International Nuclear Information System (INIS)

Yang Liu; Zhang Xin

1988-01-01

L-Tetrahydroprotoberberine (THPB) alkaloids are dopamine-receptor antagonists. Stepholidine has been shown to possess the strongest pharmacological effects among the THPB alkaloids studied. In order to study its metabolism and the mode of action of the drug, a radiolabeled stepholidine was required. We report here the synthesis of 14 C-labeled stepholidine by Mannich condensation of 7-benzyloxy-1-(4-benzyloxy-3-hydroxy-benzyl)-6-methoxy-1,2,3,4-tetrahydroisoquinoline with ( 14 C)formaldehyde followed by methylation and debensylation in 32% radiochemical yield. (author)

Synthesis of /sup 14/C-labelled milrinone

Energy Technology Data Exchange (ETDEWEB)

Duncan, D.R.; Johnston, D.; Andrews, R.S. (Stirling-Winthrop, Alnwick (UK). Research and Development Div.)

1985-02-01

A synthetic procedure for producing /sup 14/C-labelled milrinone, a potent new cardiotonic agent, is described. The synthesis was achieved in two steps from 1-(4-pyridyl)propan-2-one utilising (2-/sup 14/C)cyanoacetamide as the source of the radiolabel. The overall chemical yield was 46% and the radiochemical yield 35%.

The DSS-14 C-band exciter

Science.gov (United States)

Rowan, D. R.

1989-01-01

The development and implementation of a C-band exciter for use with the Block IV Receiver-Exciter Subsystem at Deep Space Station 14 (DSS-14) has been completed. The exciter supplements the standard capabilities of the Block IV system by providing a drive signal for the C-band transmitter while generating coherent translation frequencies for C-band (5-GHz) to S-band (2.2- to 2.3-GHz) Doppler extraction, C-band to L-band (1.6-GHz) zero delay measurements, and a level calibrated L-band test signal. Exciter functions are described, and a general explanation and description of the C-band uplink controller is presented.

Effect of level of dietary protein on the distribution of 14C-activity from exogenous 14C-inosine in chicks

International Nuclear Information System (INIS)

Masushige, Shoichi; Tadokoro, Tadahiro; Suzuki, Takao; Nakajima, Hisao.

1983-01-01

The effect of dietary protein level on the metabolic fate of intraperitoneally administered (exogeneous) 8- 14 C-inosine in chicks was studied. Three different protein level diets (low, standard and high) were prepared. Chicks were fed on these diets for 10 days, respectively and the following results were found: (1) RNA content of liver, small intestine and muscle in chicks fed on a low protein diet was decreased as compared to other diet groups, but no difference was observed in kidney or pancreas. (2) 14 C uptake by organs from exogeneous 8- 14 C-inosine was determined. The uptake of 14 C in kidney, pancreas and small intestine was higher than that in liver and muscle. Moreover, the uptake by tissues in the low protein groups was significantly higher than that in either the standard or high protein groups, but no difference was observed between these latter two groups. (3) The rate of incorporation of 14 C labelled purine by acid soluble materials and RNA was higher in kidney, pancreas and small intestine than in liver and muscle, and also higher in chicks fed on a low protein diet than in either the standard or high protein groups. (4) It was revealed that the 14 C-labelled purine rings from 8- 14 C-inosine were incorporated into AMP and GMP as constituents of RNA. (author)

Structure of 14C and 14B from the C,1514(d ,3He)B,1413 reactions

Science.gov (United States)

Bedoor, S.; Wuosmaa, A. H.; Albers, M.; Alcorta, M.; Almaraz-Calderon, Sergio; Back, B. B.; Bertone, P. F.; Deibel, C. M.; Hoffman, C. R.; Lighthall, J. C.; Marley, S. T.; Mcneel, D. G.; Pardo, R. C.; Rehm, K. E.; Schiffer, J. P.; Shetty, D. V.

2016-04-01

We have studied the C,1514(d ,3He)B,1413 proton-removing reactions in inverse kinematics. The (d ,3He ) reaction probes the proton occupation of the target ground state, and also provides spectroscopic information about the final states in B,1413. The experiments were performed using C,1514 beams from the ATLAS accelerator at Argonne National Laboratory. The reaction products were analyzed with the HELIOS device. Angular distributions were obtained for transitions from both reactions. The 14C-beam data reveal transitions to excited states in 13B that suggest configurations with protons outside the π (0 p3 /2) orbital, and some possibility of proton cross-shell 0 p -1 s 0 d excitations, in the 14C ground state. The 15C-beam data confirm the existence of a broad 2- excited state in 14B. The experimental data are compared to the results of shell-model calculations.

Synthesis of 1-benzyl-4-[(5,6-dimethoxy[2-14C]-1-indanon)-2-YL]-methylpiperidine hydrochloride (E2020-14C)

International Nuclear Information System (INIS)

Iimura, Youichi; Mishima, Mannen; Sugimoto, Hachiro

1989-01-01

1-Benzyl-4-[(5,6-dimethoxy[2- 14 C]-1-indanon)-2-yl]-methylpiperidine hydrochloride (E2020- 14 C), and acetylcholinesterase inhibitor for studying the pharmacokinetic profiles of E2020, was synthesized from 5,6-dimethoxy[2- 14 C]-1-indanone as the labelled starting material. (author)

Calibration of 14C Histograms : A Comparison of Methods

NARCIS (Netherlands)

Stolk, Ad; Törnqvist, Torbjörn E.; Hekhuis, Kilian P.V.; Berendsen, Henk J.A.; Plicht, Johannes van der

1994-01-01

The interpretation of C-14 histograms is complicated by the non-linearity of the C-14 time scale in terms of Calendar years, which may result in clustering of C-14 ages in certain time intervals unrelated to the (geologic or archaeologic) phenomenon of interest. One can calibrate C-14 histograms for

Investigation of phases obtained from the Ce.sub.20./sub.Ru.sub.60./sub.Si.sub.20./sub. composition

Czech Academy of Sciences Publication Activity Database

Vejpravová, J.; Sechovský, V.; Prokleška, J.; Daniš, S.; Jurek, Karel

2008-01-01

Roč. 466, 1-2 (2008), s. 17-25 ISSN 0925-8388 Institutional research plan: CEZ:AV0Z10100521 Keywords : rare earth compounds * laves phase * superconductivity * ternary Ce-Ru-Si system Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.510, year: 2008

Formation and bio release of bound residues of [14 C]-lindane and [14 C]-parathion in two Brazilian soils

International Nuclear Information System (INIS)

Andrea, M.M. de.

1992-01-01

This work studied the extractable and bound residues formation of 14 C-lindane and 14 C-parathion immediately after application and after 3 months of interaction of the pesticides with the soils. Metabolism, bio release, and the possible bioavailability of bound residues were studied by employing bio meter flasks which allowed a relative comparison of the behaviour of the two different 14 C-pesticides, by a balance of the applied or present radiocarbon in the soils after the bio tests. (author)

Synthesis of (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)olivetolic acid, methyl (1'-/sup 13/C)olivetolate and (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)cannabigerolic acid

Energy Technology Data Exchange (ETDEWEB)

Porwoll, J.P.; Leete, E. (Minnesota Univ., Minneapolis (USA). Dept. of Chemistry)

1985-03-01

Potential advanced intermediates in the biosynthesis of delta/sup 9/-tetrahydrocannabinol, the major psychoactive principle of marijuana, have been synthesized labeled with two contiguous /sup 13/C atoms and /sup 14/C. Methyl (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)olivetolate was prepared from lithium (/sup 13/C/sub 2/)acetylide and dimethyl (2-/sup 14/C)malonate. Reaction with geranyl bromide afforded methyl (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)cannabigerolate, and hydrolysis of these methyl esters with lithium propyl mercaptide yielded the corresponding labeled acids. The /sup 13/C-/sup 13/C couplings observable in the /sup 13/C NMR spectra of these /sup 13/C-enriched compounds and their synthetic precursors are recorded. Methyl (1'-/sup 14/C)olivetolate was prepared from /sup 13/CO/sub 2/ to confirm assignments of the /sup 13/C chemical shifts in the pentyl side chain of these compounds.

{sup 14}C emission from Swedish nuclear power plants and its effect on the {sup 14}C levels in the environment

Energy Technology Data Exchange (ETDEWEB)

Stenstroem, K.; Erlandsson, Bengt; Hellborg, R.; Kiisk, M.; Persson, Per [Lund Univ. (Sweden). Dept. of Nuclear Physics; Mattsson, Soeren; Thornberg, C. [Lund Univ., Malmoe (Sweden). Dept. of Radiation Physics; Skog, G. [Lund Univ. (Sweden). Dept. of Quaternary Geology

2000-02-15

The radionuclide {sup 14}C is produced in all types of nuclear reactors mainly by neutron induced reactions in oxygen ({sup 17}O), nitrogen ({sup 14}N) and carbon ({sup 13}C). Part of the {sup 14}C created is continuously released during normal operation as airborne effluents in various chemical forms (such as CO{sub 2}, CO and hydrocarbons) to the surroundings. Because of the biological importance of carbon and the long physical half-life of {sup 14}C, it is of interest to measure the releases and their incorporation into living material. The {sup 14}C activity concentrations in annual tree rings and air around two Swedish nuclear power plants (Barsebaeck and Forsmark) as well as the background {sup 14}C activity levels from two reference sites in southern Sweden during 1973-1996 are presented in this report. In order to verify the reliability of the method some investigations have been conducted at two foreign nuclear sites, Sellafield fuel reprocessing plant in England, and Pickering nuclear generating station in Canada, where the releases of {sup 14}C are known to be substantial. Furthermore, results from some measurements in the vicinity of Paldiski submarine training centre in Estonia are presented. The results of the {sup 14}C measurements of air, vegetation and annual tree rings around the two Swedish nuclear power plants show very low enhancements of {sup 14}C, if at all above the uncertainty of the measurements. Even if the accuracy of the measurements of the annual tree rings is rather good (1-2%) the contribution of {sup 14}C from the reactors to the environment is so small that it is difficult to separate it from the prevailing background levels of {sup 14}C . This is the case for all sampling procedures: in air and vegetation as well as in annual tree rings. Only on a few occasions an actual increase is observed. However, although the calculations suffer from rather large uncertainties, the calculated release rate from Barsebaeck is in fair agreement

Solid phase radioimmunoassays for human C-reactive protein

International Nuclear Information System (INIS)

Shine, B.; Beer, F.C. de; Pepys, M.B.

1981-01-01

Two new, rapid and sensitive radioimmunoassays for human C-reactive protein (CRP) have been established using antiserum coupled to magnetizable cellulose particles, which facilitate phase separation. A single antibody method, using solid phase anti-CRP, provides a sensitivity of 50 μg/l with a 1-h incubation time and intra- and inter-assay coefficients of variation of 10%. A double antibody method, using fluid phase rabbit anti-CRP serum and solid phase sheep anti-rabbit IgG serum, provides a sensitivity of 3 μg/l with an overnight incubation and intra- and inter-assay coefficients of variation of 10%. Among 468 sera from normal adult volunteer blood donors the median CRP concentration was 800 μg/l, interquartile range 340-1700 μg/l and range 70-29,000 μg/l. Ninety percent of samples contained less than 3 mg/l and 99% less than 10 mg/l. Low levels (14-650 μg/l) of CRP were detected both in amniotic fluids and in cerebrospinal fluids. (Auth.)

How accurate is the 14C method

International Nuclear Information System (INIS)

Nydal, R.

1979-01-01

Radiocarbon daters have in recent years focussed their interest on accuracy and reliability of 14 C dates. The use of dates for resolving fine chronological structures that are not dateable otherwise has stressed this point. The total uncertainty in dating an event is composed of errors relating to dating of the sample, i.e. uncertainty in measured quantities, deviations from assumed content of 14 C in material when alive; and errors related to quality of sample material, i.e. contamination from carbon of different age, diffuse context between sample and event. Statistical variability in counting of 14 C activity gives the most important contribution to measurement uncertainty - increasing with age and shortage of sample material. Corrections for isotopic fractionation and reservoir effects must be performed, and - most important when dates are compared with historical ages - the dendrochronological calibration will correct for past variations in the atmospheric 14 C content. Future improvement of dating precision can however only be obtained by the combined efforts of both daters and submitters of samples, thus minimizing errors related to selection and handling of sample material as well as those related to the 14 C method and measurements. (Auth.)

Clinical investigation of 14C-urea breath test

International Nuclear Information System (INIS)

Yu Yongli; Zhu Ruisen; Ji Hong; Luo Quanyong

2000-01-01

To investigate clinical value of 14 C-urea breath test ( 14 C-UBT) for the diagnosis of Helicobacter pylori(Hp), 70 patients were both performed gastroscopy (taking gastric mucosae biopsy for rapid urease test and histology) and 14 C-UBT (some patients by Hp-IgG or DNAHp test also) within two days. The positive cases of both rapid urease test and histology was defined as 'gold standard' of Hp-positive, whereas the negative cases of both rapid urease test and histology as 'gold standard' of Hp-negative. The sensitivity of 14 C-UBT was 93.2%, the specificity 73.1%, and the diagnostic accuracy 85.7%. The difference (comparing with 'gold standard') was not marked (x 2 = 0.9 0.05(1) 2 = 3.84, P>0.05). But the diagnostic accuracy of 14 C-UBT (85.7%) and Hp-IgG (50%) had a marked difference (x 2 13.80>x 0.01(1) 2 = 6.64, P 14 C-UBT was easy to operate, reliable and suitable for clinical application

Method for combined 3H and 14C autoradiography with a single emulsion tested in cultured mammalian cells

International Nuclear Information System (INIS)

Perdue, S.W.; Kimball, R.F.; Hsie, A.W.

1977-01-01

A single-gelatin expanded film method for double-isotope autoradiography is described. A preliminary classification based upon silver-grain distribution is used to assign labeled cells to 3 H only or with 14 C classes. Optical sectioning combined with grain counting is employed to obtain ratios for classifying cells labeled with 14 C into 14 C only and 3 H + 14 C classes. The method has been tested with CHO-K1 cells in plateau-phase cultures using two 24-h labeling periods. The experimental design allowed for independent estimation of the expected frequencies of label classes under conditions that provided a wide range of possible label levels and combinations. Previous methods have used time-consuming applications of two emulsion layers and exposures to distinguish between cells labeled with 3 H only or with 14 C and do not identify the 3 H + 14 C class. A single-gelatin expanded film requires only one exposure and permits all label classes to be determined by an objective grain-counting procedure

Thermal processing of diblock copolymer melts mimics metallurgy

Science.gov (United States)

Kim, Kyungtae; Schulze, Morgan W.; Arora, Akash; Lewis, Ronald M.; Hillmyer, Marc A.; Dorfman, Kevin D.; Bates, Frank S.

2017-05-01

Small-angle x-ray scattering experiments conducted with compositionally asymmetric low molar mass poly(isoprene)-b-poly(lactide) diblock copolymers reveal an extraordinary thermal history dependence. The development of distinct periodic crystalline or aperiodic quasicrystalline states depends on how specimens are cooled from the disordered state to temperatures below the order-disorder transition temperature. Whereas direct cooling leads to the formation of documented morphologies, rapidly quenched samples that are then heated from low temperature form the hexagonal C14 and cubic C15 Laves phases commonly found in metal alloys. Self-consistent mean-field theory calculations show that these, and other associated Frank-Kasper phases, have nearly degenerate free energies, suggesting that processing history drives the material into long-lived metastable states defined by self-assembled particles with discrete populations of volumes and polyhedral shapes.

Fate of 14C-labelled compounds in marine environment

International Nuclear Information System (INIS)

Kale, S.P.; Raghu, K.; Sherkhane, P.D.; Murthy, N.B.K.

1999-01-01

Model ecosystems have played an important role in predicting environmental behavior of agrochemicals. The microcosms used in these studies generally include soil units containing usual biotic components common for that ecosystem. In present studies, scope of two such ecosystems has been extended to study the fate of 14 C-labelled pesticides in marine environment. 14 C-labelled pesticides used in these studies were chlorpyrifos, DDT and HCH. Two systems were developed in laboratory simulating marine environment to study the fate of these pesticides. The first system was developed in an all glass aquarium tank with marine sediments, seawater, clams and algae and is referred to as marine ecosystem. The second system was developed to permit the total 14 C-mass balance studies. It contained marine sediments under moist (60% water holding capacity) or flooded conditions and it is referred to as continuous flow system. Fate of 14 C-DDT was studied in marine ecosystem while degradation of 14 C-chlorpyrifos and 14 C-HCH was studied in continuous flow system. 14 C-DDT did not bioaccumulate in clams while at the end of 60 days 50% of the applied 14 C-activity was present in sediment fraction of marine ecosystem. 14 C-HCH degradation showed about 22-26% mineralization while 45-55% of the applied activity was recovered as organic volatiles. No significant bound residues were formed. 14 C-chorpyrifos underwent considerable degradation in marine environment. TCP was the major degradation product. (author)

Radioactive waste with 14C in Argentina

International Nuclear Information System (INIS)

Di Lello, D.S.

2009-01-01

14 C is a long half-life radioisotope, which is present in radioactive waste generated during the operation and decommissioning of nuclear power plants. 14 C can also be found in waste generated by medical diagnostic laboratories or any one generated by fields that deal with research and development (mainly connected with the biochemists area). According to international precedents the disposal of 14 C based on the final amount found in radioactive waste and its chemical form have conditioned the design and operation of the facilities (either because of the amount of it or the chemical form in which 14 C was present). We have to take into account that the design of facilities for radioactive waste disposal is included among the obligations of the National Radioactive Waste Management Program (PNGRR). It is absolutely necessary to count with enough information about the characteristics of any waste containing 14 C that is generated in Argentina, in order to be able to fulfil the requirements previously mentioned. The main characteristics of interest in the frame of the present project are: a) the principal reactions that take place for the formation of 14 C; b) The specific concentration of activity in materials where this radio nuclei is formed or is accumulated; c) To know which is the current step in the process of managing these wastes (in Argentina and all over the world). Either if it refers to bulk or conditioned storage, inside the generating facility; d) Transportation possibilities of 14 C under these conditions; e) The accumulated volume and the generation rate of this kind of waste in Argentina. This paper presents an initial collection and evaluation of the information related to the characteristics already mentioned, having gathered published material from the literature and information in the PNGRR up to this moment. The description of the characteristics of the radioactive waste containing 14 C from nuclear power plants, hospitals and research and

Spheroidization behavior of dendritic b.c.c. phase in Zr-based モ-phase composite

Directory of Open Access Journals (Sweden)

Sun Guoyuan

2013-03-01

Full Text Available The spheroidization behavior of the dendritic b.c.c. phase dispersed in a bulk metallic glass (BMG matrix was investigated through applying semi-solid isothermal processing and a subsequent rapid quenching procedure to a Zr-based モ-phase composite. The Zr-based composite with the composition of Zr56.2Ti13.8Nb5.0Cu6.9Ni5.6Be12.5 was prefabricated by a water-cooled copper mold-casting method and characterized by X-ray diffraction (XRD and scanning electron microscope (SEM. The results show that the composite consists of a glassy matrix and uniformly distributed fine dendrites of the モ-Zr solid solution with the body-centered-cubic (b.c.c. structure. Based on the differential scanning calorimeter (DSC examination results, and in view of the b.c.c. モ-Zr to h.c.p. メ-Zr phase transition temperature, a semi-solid holding temperature of 900 ìC was determined. After reheating the prefabricated composite to the semi-solid temperature, followed by an isothermal holding process at this temperature for 5 min, and then quenching the semi-solid mixture into iced-water; the two-phase microstructure composed of a BMG matrix and uniformly dispersed spherical b.c.c. モ-Zr particles with a high degree of sphericity was achieved. The present spheroidization transition is a thermodynamically autonomic behavior, and essentially a diffusion process controlled by kinetic factors; and the formation of the BMG matrix should be attributed to the rapid quenching of the semi-solid mixture as well as the large glass-forming ability of the remaining melt in the semi-solid mixture.

Studies on dissipation and degradation of 14 C-DDT and 14 C-parathion in egyptian soil under field conditions

International Nuclear Information System (INIS)

Ezz El-Arab, A.; Mostafa, I.Y.

1991-01-01

The rates of dissipation and degradation of the insecticides DDT and parathion were studied under field conditionsm using 14 C-labelled chemicals. Over a period of 12 weeks, extractable, soil-bound and total 14 C-activity were recorded. In case of DDT, dissipation of 14 C-activity from soil showed a continuous and gradual increase reaching about 30% after 8 weeks and remained constant up to 12 weeks. The formation of DDE as a principal metabolite seems to be increasing with time ans accounted for approximately 25% of the extractable residues after 12 weeks. There was also a gradual significant increase in the formation of soil 14 C-bound residues which reached 12% of the total residues after the same period. On the other hand, parathion dissipation from the soil under the same conditions did not exceed 10% up to 12 weeks. The amount of 14 C-bound residues was found to contribute 33% of the applied dose. Analysis of the extractable fraction revealed that parathion was partly degraded by soil microorganisms into p-amino phenol, p-nitrophenol, paraoxon, amino parathion and aminoparaoxon in different percentages depending on the depth of soil. 2 fig.,1 tab

14C Carbofuran residue in rice-fish ecosystem model

International Nuclear Information System (INIS)

Sumatra, M.; Soekarna, D.; Suhanda; Kuswadi, A.N.

1988-01-01

14-C-carbofuran in the form of 14-C-Furada 3G was applied with doses of 0, 2, and 4 g/m2 to a rice-fish ecosystem model consisting of water, soil, rice, plant, and fish (Cyprinus carpio) in tanks of the size 1 m length, 1 m width, and 0.5 m depth. 14-C-carbofuran was released from 14-C-Furadan 3G, entered into the water, absorbed by plant root, and then distributed into the whole plant. A part of the 14-C-carbofuran was absorbed and retained by soil. In both doses of 4 and 2 g/m2, the 14-C-Furadan 3G was toxic to Cyprinus carpio under this experiment condition. (author). 5 refs, 5 figs, 6 tabs

14C-Methylenebisphenylisocyanate (14C-MDI). Study of absorption after single dermal and intradermal administration in rats

International Nuclear Information System (INIS)

Leibold, E.; Hoffmann, H.D.; Hildebrand, B.

1999-01-01

The absorption, distribution and excretion of radioactivity was studied in groups of four male Wistar rats following a single dermal and intradermal administration of 14 C- Methylenebisphenylisocyanate ( 14 C-MDI) at nominal dose levels of 4.0 and 0.4 mg/cm 2 for dermal administration and 0.4 mg/animal for intradermal administration. These dose levels nominally corresponded to 40 and 4.0 mg/animal for dermal administration. Considering the animal weights, dose levels corresponded to about 140 and 14 mg/kg body weight (dermal administration) and 1.4 mg/kg body weight (intradermal administration). In the experiments with dermal administration, animals were exposed for 8 hours and sacrificed 8, 24 or 120 h after beginning of exposure. In the experiment with intradermal administration, animals were sacrificed 120 h after treatment. After dermal administration of 14 C-MDI, mean recoveries of radioactivity from all dose groups were in the range from 97.86 to 108.07% of the total radioactivity administered. Generally, the largest proportion of radioactivity was found at the application site and dressing. The total amount of radioactivity absorbed (including excreta, cage wash, tissues/organs and carcass) increased with increasing sacrifice time. Dermal absorption was very low and quantitatively similar at both dose levels; maximally ca. 0.9 % of the applied radioactivity was absorbed. After intradermal administration of 14 C-MDI, the mean recovery of radioactivity was 100.90 % of the radioactivity administered. The largest proportion of radioactivity was found at the application site. The total amount of radioactivity absorbed (including excreta, cage wash, tissues/organs and carcass) amounted to about 26 % of the radioactivity applied. Irrespective of the mode of administration of 1 4C -MDI, concentrations of radioactivity in tissues and organs generally were below 1 μg Eq/g at 120 h after administration. In summary, the results of this study comparing systemic

Application of AMS 14C measurements to criminal investigations

International Nuclear Information System (INIS)

Nakamura, T.; Ohta, T.; Nishida, M.; Rakowski, A.; Ikeda, A.; Oda, H.; Kojima, S.

2007-01-01

14 C variations of atmospheric CO 2 as well as carbonaceous fraction of living materials, such as collagen from tooth and bone, tissue, skin, hair, nail, etc., of modern humans are influenced by 14 C produced artificially by nuclear bomb tests in the atmosphere from late 1950s to early 1960s. By careful investigation of 14 C concentration of tree rings and human body samples formed in this time intervals, we can establish a relationship of their 14 C concentrations with calendar year. By applying this relation to a sample whose 14 C concentration can be measured, we can estimate the formation age of the sample. In addition, sources of the chemicals that were used in some criminal cases can be possibly identified, by their carbon isotope ratios ( 13 C/ 12 C and 14 C/ 12 C). This method of age determination has been applied to a forensic study, i.e., two criminal cases of murder. For each case, by comparing the measured 14 C abundances of several pieces of hair and one tooth (the third molar) from the body with the annual change on concentrations of bomb-produced 14 C, the time of death of the body and the age of the victim were estimated. The estimated values were consistent with the real ones that were revealed by the confession of the real murderers. (author)

{8-14C}-Adenine and {1-14C}-isopentenyl pyrophosphate - precursors for root-produced cytokinins in the tomato (Lycopersicon esculentum mill.)

International Nuclear Information System (INIS)

Dickinson, J.R.

1985-01-01

Following the detection of reasonable levels of biologically active cytokinin-like compounds in one-month-old tomato plants, the possible involvement of {8- 14 C}-adenine and {1- 14 C}-isopentenyl pyrophosphate in the biosynthetic pathway leading to an accumulation of free zeatin derivatives, was studied. Intact tomato plants were used for a time-course study involving the uptake of {8- 14 C}-adenine and the tentative identification of compounds into which the 14 C became incorporated. Using high performance liquid chromatography, radioactive trans-zeatin was identified as being present in the Dowex 50 root extract. The 12-hour time interval was used and the roots of the tomato plants were immersed in a more heavily radiolabelled medium. Modified separation techniques were used to achieve enhanced radioactivity recovery rates. This experiment demonstrated the presence of relatively high levels of tentatively identified radioactive zeatin in the Dowex 50 root and stem extracts. Radioactivity in the aqueous extracts was found not to be contributed by cytokinin nucleotides. A final experiment was carried out using decapitated root systems to determine if the root tissue alone could be implicated in the synthesis of cytokinins. Decapitated tomato root systems were supplied with either {8- 14 C}-adenine or {1- 14 C}-isopentenyl pyrophosphate. The ratio of incorporation of {1- 14 C}-isopentenyl pyrophosphate into identified cytokinins was higher than for {8- 14 C}-adenine. It was concluded that both adenine and isopentenyl pyrophosphate are involved in the biosynthetic pathway leading to an accumulation of free zeatin derivatives in tomato roots

Autoradiographic disposition of [1-methyl-14C]- and [2-14C]caffeine in mice

International Nuclear Information System (INIS)

Lachance, M.P.; Marlowe, C.; Waddell, W.J.

1983-01-01

Male, C57B1/6J mice received either [1-methyl-14C]caffeine or [2-14C]caffeine via the tail vein at a dose of 0.7 or 11 mg/kg, respectively. At 0.1, 0.33, 1, 3, 9, and 24 hr after treatment, the mice were anesthetized with ether and frozen by immersion in dry ice/hexane. The mice were processed for whole-body autoradiography by the Ullberg technique; this procedure does not allow thawing or contact with solvents. All autoradiographs revealed some retention of radioactivity at early time intervals in the lacrimal glands, seminal vesicle fluid, nasal and olfactory epithelium, and retinal melanocytes. The remaining portion of the animal was densitometrically uniform except for the lower levels noted in the CNS and adipose tissues. Excretion of radioactivity by the liver and kidneys seems to be the major routes of elimination. Localization in the liver at late time intervals was confined principally to the centrilobular region. Late sites of retention, observed only after [1-methyl-14C]caffeine administration, included the pancreas, minor and major salivary glands, splenic red pulp, thymal cortex, bone marrow, and gastrointestinal epithelium. Sites of localization present in both studies included the olfactory epithelium, lacrimal glands, hair follicles, and retinal melanocytes. Further studies are needed to determine whether the localization at these various sites is due to metabolic degradation, active transport, or possibly a specific receptor interaction

Magnitude of 14C/12C variations based on archaeological samples

International Nuclear Information System (INIS)

Kusumgar, S.; Agrawal, D.P.

1977-01-01

The magnitude of 14 C/ 12 C variations in the period A.D. 5O0 to 200 B.C. and 370 B.C. to 2900 B.C. is discussed. The 14 C dates of well-dated archaeological samples from India and Egypt do not show any significant divergence from the historical ages. On the other hand, the corrections based on dendrochronological samples show marked deviations for the same time period. A plea is, therefore, made to study old tree samples from Anatolia and Irish bogs and archaeological samples from west Asia to arrive at a more realistic calibration curve. (author)

Preparation and HPLC isolation of L-[U-14C]tryptophan from enzyme hydrolysate labelled with 14C

International Nuclear Information System (INIS)

Novak, J.; Tintera, S.; Hromadkova, B.

1990-01-01

Tryptophan was obtained from biomass of the blue-green alga Synechococcus elongatus cultivated under 14 CO 2 . After partial purification, the protein fraction was subjected to enzymatic hydrolysis using pronase. Semipreparative isolation of L-[U- 14 C]tryptophan was accomplished on a HPLC column of Separon S Hema 1000 CM, 2% ethanol were added to the eluent, and a precolumn packed with the basic anion exchanger Spheron 1000 DEAE was used. Always after the passage of L-[U- 14 C]tryptophan, the precolumn was decoupled. The substance was collected in 96% ethanol. After removing the solvent by vacuum evaporation, the sample was analyzed on a column packed with Separon SIX C 18 in the eluent of 0.1M-NaH 2 PO 4 , 2% methanol. When the desired radiochemical purity was not attained, the sample was purified on Separon SIX C 18 using 2% methanol. The final radiochemical purity achieved by using this method is 98%. (P.A.). 5 figs., 2 tabs., 4 refs

The bomb 14C transient in the Pacific Ocean

Science.gov (United States)

Rodgers, Keith B.; Schrag, Daniel P.; Cane, Mark A.; Naik, Naomi H.

2000-04-01

A modeling study of the bomb 14C transient is presented for the Pacific Ocean. A primitive equation ocean circulation model has been configured for a high-resolution domain that accounts for the Indonesian Throughflow (ITF). Four separate runs were performed: (1) seasonal forcing with 20 Sv of ITF transport, (2) seasonal forcing with 10 Sv of ITF transport, (3) seasonal forcing with no ITF transport, and (4) interannual forcing with 15 Sv of ITF transport. This study has two main objectives. First, it is intended to describe the time evolution of the bomb 14C transient. This serves as a tool with which one can identify the physical processes controlling the evolving bomb 14C distribution in the Pacific thermocline and thus provides an interpretive framework for the database of Δ14C measurements in the Pacific. Second, transient tracers are applied to the physical oceanographic problem of intergyre exchange. This is of importance in furthering our understanding of the potential role of the upper Pacific Ocean in climate variability. We use bomb 14C as a dye tracer of intergyre exchange between the subtropical gyres and the equatorial upwelling regions of the equatorial Pacific. Observations show that while the atmospheric Δ14C signal peaked in the early to mid-1960s, the Δ14C levels in the surface water waters of the subtropical gyres peaked near 1970, and the Δ14C of surface waters in the equatorial Pacific continued to rise through the 1980s. It is shown that the model exhibits skill in representing the large-scale observed features observed for the bomb 14C transient in the Pacific Ocean. The model successfully captures the basin-scale inventories of bomb 14C in the tropics as well as in the extratropics of the North Pacific. For the equatorial Pacific this is attributed to the model's high meridional resolution. The discrepancies in the three-dimensional distribution of bomb 14C between the model and data are discussed within the context of the dynamical

Biodegradation mechanism of linear alkylbenzenesulfonate-14C

International Nuclear Information System (INIS)

Kubodera, Tadayoshi; Muto, Toshio; Yamamoto, Tatsuo

1978-01-01

The biodegradation of linear alkylbenzenesulfonate- 14 C (LAS- 14 C) tagged with 14 C at the linear side chain was studied on activated sludge by tracer method in addition to the methylene blue method which is widely employed in the biodegradation of LAS. It was found that there were three periods of rapid adsorption period, acclimation period, and degradation process. The radiolysis of dodecylbenzenesulfonate was studied on irradiating by 5000 Ci 60 Co source. The decomposition products were identified by GLC and GC-MS spectrometry after desulfonation. 1-Tetralone, 1-indanone, 4-methyl-1-tetralone, naphthalene et al. were found in them. (author)

Synthesis of {sup 14}C-labeled levamisole and {sup 13}C-labeled tetramisole

Energy Technology Data Exchange (ETDEWEB)

Feil, V.J. [US Department of Agriculture, Agricultural Research Service, Biosciences Research Lab., Fargo, ND (United States)

1996-12-01

The syntheses of {sup 14}C-ring labeled levamisole ([-]-2,3,5,6-tetrahydro-6-phenyl [{sup 14}C]-UL imidazo[2,1-b]thiazole) from acetophenone-ring-UL-{sup 14}C in 5 steps plus resolution with a 7.5% overall yield, and {sup 13}C{sub 6}-ring labeled tetramisole ([{+-}]-2,3,5,6-tetrahydro-6-phenyl [{sup 13}C{sub 6}]imidazo[2,1-b]thiazole) from benzene-{sup 13}C{sub 6} in 6 steps with a 9.0% overall yield are described. (author).

Synthesis of [14C]-labelled AY-30,068

International Nuclear Information System (INIS)

Hicks, D.R.; Hangeland, J.J.; Mobilio, D.; DeLange, B.

1988-01-01

[ 14 C]AY-30,068 (cis-1,8-diethyl-2,3,4,9-tetrahydro-4-(2-propenyl)-1H-carbazole-1-acetic acid), a potent analgesic agent, was prepared by incorporating [ 14 C]methyl iodide via a Wittig reaction. The intermediate aldehyde was synthesized in six steps from cis-1-ethyl-2-oxo-4-(2-propenyl)cyclohexaneacetic acid methyl ester. Three batches of the [ 14 C]labelled AY-30,068 were produced, giving a combined overall yield of 9% from [ 14 C]methyl iodide sp. act. 51.2, 17.7 and 4.4 μCi/mg; 97.5, 98.3, and 98.6% radiochemical purity, respectively. (author)

Measurement of C-14 distribution in forest around nuclear facilities

International Nuclear Information System (INIS)

Atarashi-Andoh, Mariko; Amano, Hikaru; Arakhatoon, Jahan

2003-01-01

A simple analytical method of C-14 measurement using fast bomb combustion and liquid scintillation counting (LSC) has been developed for measuring C-14 distribution in the terrestrial environment. Specific activities of C-14 in cedar leaves and soils collected from an area around nuclear facilities and control areas were measured using this method. Depth distribution of Cs-137 in soils was also measured at the same sampling sites and compared with the depth distribution of C-14. C-14 specific activity in cedar leaves examined around nuclear facilities exceeded that in the control areas by 8 to 30 mBq (g carbon) -1 . The depth distribution of C-14 in forest soil shows that C-14 has peak values in the top 10 cm of the soil profiles ascribed to the highest bomb C-14 level in the 1960's. The data were made available to assess the behavior of fallout C-14 in the surface environment. (author)

Analysis of Δ14C variations in atmosphere

International Nuclear Information System (INIS)

Simon, J.; Sivo, A.; Richtarikova, M.; Holy, K.; Polaskova, A.; Bulko, M.; Hola, O.

2005-01-01

The Δ 14 C in the atmosphere have been measured and studied in two localities of Slovakia. The accomplished analysis proved the existence of the annual variations of the Δ 14 C with the attenuating amplitude and decreasing mean value. It seems to be logical and physically correct to describe the Δ 14 C time-dependence by the equation: y = Ae -at + Be -bt cos(ω 1 t + (φ)). The coefficients A, a, B, b, (φ) are listed in the table for both the localities. The observed variations of the Δ 14 C have a maximum in summer and minimum in winter .Probably it is caused by the higher requirement of the heat supply in winter season which is connected directly with the fossil CO 2 emissions and more intensive Suess effect. Summer maximum could be explained by the combination of the lower CO 2 emission rate and higher turbulent transport of the stratospheric 14 C to the troposphere. Using the Fourier harmonic analysis the amplitude spectra of the average annual variations were plotted. The obtained result shows that the variations have the high degree of symmetry. Furthermore, the obtained basic frequency ω 1 = 2π/12 [month -1 ] proves that the cyclic processes with the period of T = 12 [month] have a major influence on the 14 C amount in the troposphere. The presence of some higher-order harmonics is significant, but a physical interpretation has not yet been clear. In addition to the main frequency there are presented also 2ω 1 and 3ω 1 in Bratislava and 4ω 1 in Zlkovce data-set. The long-time average of the Δ 14 C in Zlkovce during years 1995-2004 is higher of about 6.6 o / oo than in Bratislava. It represents an unique evidence that the local CO 2 pollution affects the 14 C activity . The correlation on the level R 2 = 0,43 was found between Bratislava and Zlkovce atmospheric Δ 14 C data. (authors)

Organic compounds preparation with 14 C

International Nuclear Information System (INIS)

Shirvani, Gholam Hossein.

1996-09-01

Active urea is a basic reagent for the synthesis of active uric-8- 14 C acid. In our manner, activated Barium carbonate with specified activity was placed in a special furnace with ability of passing gases. Then, ammonia gas was passed through it at about 850 Degree C to obtain Barium Cyanamide. Reaction of the produced compound with CO 2 , and then acidification of the mixture, gave activated urea. Condensation of the urea with Ethylcyanoacetate, produce 6-Aminouracil which upon nitrosation, reduction and then condensation with urea, the desired Uric-8- 14 C acid was synthesized. (author). 148 refs.,

Review of C-14 inventory for the SFR facility

Energy Technology Data Exchange (ETDEWEB)

Smith, Graham; Merino, Joan; Kerrigan, Emma

2002-08-01

The Swedish Radiation Protection Authority (SSI) is currently reviewing SKB's continuing assessment for disposal of radioactive waste to the SFR facility at Forsmark. Among the wastes disposed are reactor operating wastes. Among the relevant radionuclides is C-14, which is relatively difficult to measure and to control because of its mobility. This report documents a review of the C-14 inventory material submitted by SKB for the SFR-facility, to determine its validity and comment on the appropriate assumptions for C-14 content of wastes due to be disposed of to the SFR. The review is based on information provided by SSI as well as other relevant international experience. Conclusions are drawn upon: the chemical form of the C-14 in the waste from BWRs and PWRs; the production rate of C-14 in BWRs and PWRs and quantification of the source term in the IEX waste; the distribution of the C-14 in the IEX waste from BWR between the resins used for treatment of the primary cooling water and the resins used for treatment of the condensate water; quantification of the uncertainties. A suggestion is made that the C-14 inventory could be better developed based upon a mass balance assessment of all the C-14 produced in reactors, and its ultimate fate in effluent and solid wastes, taking account of the reactor specific operational factors identified in the review as relevant to C-14 inventory assessment.

Review of C-14 inventory for the SFR facility

International Nuclear Information System (INIS)

Smith, Graham; Merino, Joan; Kerrigan, Emma

2002-08-01

The Swedish Radiation Protection Authority (SSI) is currently reviewing SKB's continuing assessment for disposal of radioactive waste to the SFR facility at Forsmark. Among the wastes disposed are reactor operating wastes. Among the relevant radionuclides is C-14, which is relatively difficult to measure and to control because of its mobility. This report documents a review of the C-14 inventory material submitted by SKB for the SFR-facility, to determine its validity and comment on the appropriate assumptions for C-14 content of wastes due to be disposed of to the SFR. The review is based on information provided by SSI as well as other relevant international experience. Conclusions are drawn upon: the chemical form of the C-14 in the waste from BWRs and PWRs; the production rate of C-14 in BWRs and PWRs and quantification of the source term in the IEX waste; the distribution of the C-14 in the IEX waste from BWR between the resins used for treatment of the primary cooling water and the resins used for treatment of the condensate water; quantification of the uncertainties. A suggestion is made that the C-14 inventory could be better developed based upon a mass balance assessment of all the C-14 produced in reactors, and its ultimate fate in effluent and solid wastes, taking account of the reactor specific operational factors identified in the review as relevant to C-14 inventory assessment

Secretin enhances [14C]erythritol clearance in unanesthetized dogs

International Nuclear Information System (INIS)

Lewis, M.H.; Baker, A.L.; Dhorajiwala, J.; Moossa, A.R.

1982-01-01

To determine the effect of secretin infusion on clearance of inert markers into bile, unanesthetized dogs fitted with Thomas cannulas received continuous infusions of [ 14 C]erythritol and [ 3 H]inulin throughout study. Taurocholic acid administered sequentially at 9.0, 20.0, and 40.0 mumol/min enhanced [ 14 C]erythritol clearance, and GIH secretin (3 units/min) administered along with TCA (40.0 mumol/min) increased [ 14 C]erythritol clearance from 4.9 +/- 1.2 ml/10 min to 6.8 +/- 1.3 ml/10 min (P less than 0.001), but simultaneously measured [ 3 H]inulin clearance was unaltered. Secretin alone also increased [ 14 C]erythritol clearance but did not alter [ 3 H]inulin clearance. The increase in [ 14 C]erythritol clearance per unit increase in bile flow was less during secretin infusion than TCA. Thus, secretin increases [ 14 C]erythritol transport through restricted channels, probably distal to the canaliculi. [ 14 C]Erythritol may not be an accurate marker for canalicular bile flow in dogs during secretin infusion

Constraining processes of landscape change with combined in situ cosmogenic 14C-10Be analysis

Science.gov (United States)

Hippe, Kristina

2017-10-01

Reconstructing Quaternary landscape evolution today frequently builds upon cosmogenic-nuclide surface exposure dating. However, the study of complex surface exposure chronologies on the 102-104 years' timescale remains challenging with the commonly used long-lived radionuclides (10Be, 26Al, 36Cl). In glacial settings, key points are the inheritance of nuclides accumulated in a rock surface during a previous exposure episode and (partial) shielding of a rock surface after the main deglaciation event, e.g. during phases of glacier readvance. Combining the short-lived in situ cosmogenic 14C isotope with 10Be dating provides a valuable approach to resolve and quantify complex exposure histories and burial episodes within Lateglacial and Holocene timescales. The first studies applying the in situ14C-10Be pair have demonstrated the great benefit from in situ14C analysis for unravelling complex glacier chronologies in various glacial environments worldwide. Moreover, emerging research on in situ14C in sedimentary systems highlights the capacity of combined in situ14C-10Be analysis to quantify sediment transfer times in fluvial catchments or to constrain changes in surface erosion rates. Nevertheless, further methodological advances are needed to obtain truly routine and widely available in situ14C analysis. Future development in analytical techniques has to focus on improving the analytical reproducibility, reducing the background level and determining more accurate muonic production rates. These improvements should allow extending the field of applications for combined in situ14C-10Be analysis in Earth surface sciences and open up a number of promising applications for dating young sedimentary deposits and the quantification of recent changes in surface erosion dynamics.

Electrochemical Properties of Hydrogen-Storage Alloys ZrMn{sub 2}Ni{sub x} and ZrMnNi{sub 1+x} for Ni-MH Secondary Battery

Energy Technology Data Exchange (ETDEWEB)

Park, Hye Ryoung [Faculty of Applied Chemistry, Chonnam National University, Kwangju (Korea); Kwon, Ik Hyun [Automobile High-Technology Research Institute, Division of Advanced Materials Engineering, Chonbuk National University, Chonju (Korea)

2001-04-01

In order to improve the performance of AB{sub 2}-type hydrogen-storage alloys for Ni-MH secondary battery, AB{sub 2}-type alloys, ZrMn{sub 2}Ni{sub x}(x=0.0, 0.3, 0.6, 0.9 and 1.2) and ZrMnNi{sub 1+x}(x=0.0, 0.1, 0.2, 0.3 and 0.4) were prepared as the Zr-Mn-Ni three component alloys. The hydrogen-storage and the electrochemical properties were investigated. The C14 Laves phase formed in all alloys of ZrMn{sub 2}Ni{sub x}(x=0.0 {approx} 1.2). The equilibrium plateau pressure of the alloy, ZrMn{sub 2}Ni{sub 0.6}-H{sub 2} system, was about 0.5 atm at 30 degree C. Among these alloys, ZrMn{sub 2}Ni{sub 0.6} was the easiest to activate, and it had the largest discharge capacity as well as the best cycling performance. The C14 Laves phase also formed in all alloys of ZrMnNi{sub 1+x}(x=0.0 {approx} 0.4). The equilibrium plateau pressure of the alloy, ZrMnNi{sub 1.0}-H{sub 2} system, was about 0.45 atm at 30 degree C. Among these alloys, ZrMnNi{sub 1.0} was the easiest to activate, taking only 3 charge-discharge cycles, and it had the largest discharge capacity of 42 mAh/g. Among these alloys, ZrMn{sub 2}Ni{sub x}(x=0.0 {approx} 1.2) and ZrMnNi{sub 1+x}(x=0.0 {approx} 0.4), ZrMnNi{sub 1.0} had the largest discharge capacity (maximum value of 42 mAh/g), and it showed the fastest activation and good cycling performance. 23 refs., 4 figs., 2 tabs.

Electro-removal of H-3 and C-14 contained in scintillation liquid absorbed in soils type Phaeozem; Electrorremocion de H-3 y C-14 contenidos en liquido de centelleo absorbidos en suelos tipo Phaeozem

Energy Technology Data Exchange (ETDEWEB)

Valdovinos, V.; Bustos, E. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, Parque Tecnologico Queretaro s/n, San Fandila, 76703 Pedro Escobedo, Queretaro (Mexico); Monroy G, F., E-mail: vvaldovinos@cideteq.mx [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

2014-10-15

This paper presents the results of electro-removal, an electrochemical treatment in soils contaminated with H-3 and C-14 contained in scintillation liquids absorbed in soils. For this purpose the best electrochemical conditions were used, which are: scintillation liquid Ultima Gold Xr, water (1:1) and 1 m A in the passage of current. The media were characterized before and after of applying the different potentials by various analytical techniques, such as: liquids by gas chromatography with a flame ionization detector, solids and liquids by Fourier transform infrared spectroscopy (Ftir) and electrodes by scanning electron microscopy with elemental analysis by energy-dispersive X-ray spectroscopy. Later standard samples with H-3 and C-14 were prepared and the electrochemical treatment was applied to previously established conditions. After electrochemical treatment the scintillation liquid characterization was performed by gas chromatography and a scintillation counter to see the disintegrations per minute. According to results of Ftir, soils show no deterioration and in the liquid phase the amount of water increases as the applied potential, due to oxidation-reduction reactions where happen modification or mineralization of organic molecules (H{sub 2}O and CO{sub 2} formation). In 4 h of treatment, removal percentages in the liquid phase, were: 53.6% of H-3 and 11.6% of C-14. (Author)

A new f.c.c. phase in yttrium films

International Nuclear Information System (INIS)

Kaul, V.K.; Srivastava, O.N.

1976-01-01

A new polymorphic phase characterised by a face-centered cubic structure, with lattice parameter 5.83 +- 0.02A, has been identified in thin films of yttrium. Electron diffraction evidence and electrical resistivity measurements have been carried out in order to detect the new f.c.c. phase. (Auth.)

14C analysis via intracavity optogalvanic spectroscopy

International Nuclear Information System (INIS)

Murnick, Daniel; Dogru, Ozgur; Ilkmen, Erhan

2010-01-01

A new ultra sensitive laser-based analytical technique, intracavity optogalvanic spectroscopy (ICOGS), allowing extremely high sensitivity for detection of 14 C-labeled carbon dioxide has recently been demonstrated. Capable of replacing accelerator mass spectrometers (AMS) for many applications, the technique quantifies zeptomoles of 14 C in sub micromole CO 2 samples. Based on the specificity of narrow laser resonances coupled with the sensitivity provided by standing waves in an optical cavity, and detection via impedance variations, limits of detection near 10 -1514 C/ 12 C ratios have been obtained with theoretical limits much lower. Using a 15 W 14 CO 2 laser, a linear calibration with samples from 5 x 10 -15 to >1.5 x 10 -12 in 14 C/ 12 C ratios, as determined by AMS, was demonstrated. Calibration becomes non-linear over larger concentration ranges due to interactions between CO 2 and buffer gas, laser saturation effects and changes in equilibration time constants. The instrument is small (table top), low maintenance and can be coupled to GC or LC input. The method can also be applied to detection of other trace entities. Possible applications include microdosing studies in drug development, individualized sub-therapeutic tests of drug metabolism, carbon dating and real time monitoring of atmospheric radiocarbon.

15C-15F Charge Symmetry and the 14C(n,γ)15C Reaction Puzzle

International Nuclear Information System (INIS)

Timofeyuk, N.K.; Thompson, I.J.; Baye, D.; Descouvemont, P.; Kamouni, R.

2006-01-01

The low-energy reaction 14 C(n,γ) 15 C provides a rare opportunity to test indirect methods for the determination of neutron capture cross sections by radioactive isotopes versus direct measurements. It is also important for various astrophysical scenarios. Currently, puzzling disagreements exist between the 14 C(n,γ) 15 C cross sections measured directly, determined indirectly, and calculated theoretically. To solve this puzzle, we offer a strong test based on a novel idea that the amplitudes for the virtual 15 C→ 14 C+n and the real 15 F→ 14 O+p decays are related. Our study of this relation, performed in a microscopic model, shows that existing direct and some indirect measurements strongly contradict charge symmetry in the 15 C and 15 F mirror pair. This brings into question the experimental determinations of the astrophysically important (n,γ) cross sections for short-lived radioactive targets

Behavior of 14C-BHC residues in rice grain

International Nuclear Information System (INIS)

Lee, S.R.; Kim, Y.H.

1981-01-01

γ-(U- 14 C)-BHC was applied to rice plants grown in a pot and its fate in the growth, polishing and oil-extraction processes of the grain was investigated. The 14 C-activity was absorbed and translocated widely in the plant and the recovery of applied 14 C-activity in the straw and grain was about 2.8%, of which 9.4% was found in the brown rice. The % partitioning of 14 C-residues in bran and polished rice was 12:88 and that in oil and oilcake was 37:63. Characterization of 14 C-residues the presence of γ-BHC, pentachlorocyclohexene, trichlorobenzene and hydrophilic metabolites, whose proportions were different in the straw and grain. (Author)

Appearance of circulating and tissue 14C-lipids after oral 14C-tripalmitate administration in the late pregnant rat

International Nuclear Information System (INIS)

Argiles, J.; Herrera, E.

1989-01-01

Studies were performed to determine whether and/or how dietary lipids participate in maternal hypertriglyceridemia during late gestation in the rat. After oral administration of glycerol-tri(1-14C)-palmitate, total radioactivity in plasma increased more rapidly in 20-day pregnant rats than in either 19-day pregnant rats or virgin controls. At the peak of plasma radioactivity, four hours after the tracer was administered, most of the plasma label corresponded to 14C-lipids in triglyceride-rich lipoproteins (d less than 1.006), and when expressed per micromol of triglyceride, values were higher in pregnant than in virgin rats. The difference was less after 24 hours, although at this time the level of 14C-lipids in d less than 1.006 lipoproteins was still higher in 20-day pregnant rats than in virgins. Tissue 14C-lipids, as expressed per gram of fresh weight, were similar in pregnant and virgin rats, but the values in mammary glands were much higher in the former group. Estimated recovery of administered radioactivity four hours after tracer in total white adipose tissue, mammary glands, and plasma lipids was higher in pregnant than in virgin rats. No difference was found between 20-day pregnant and virgin rats either in the label retained in the gastrointestinal tract or in that exhaled as 14C-CO2 during the first four hours following oral administration of 14C-tripalmitate. These findings plus the known maternal hyperphagia, indicate that in the rat at late pregnancy triglyceride intestinal absorption is unchanged or even enhanced and that dietary lipids actively contribute to both maternal hypertriglyceridemia and lipid uptake by the mammary gland

Accelerator mass spectrometry analysis of "1"4C-oxaliplatin concentrations in biological samples and "1"4C contents in biological samples and antineoplastic agents

International Nuclear Information System (INIS)

Toyoguchi, Teiko; Kobayashi, Takeshi; Konno, Noboru; Shiraishi, Tadashi; Kato, Kazuhiro; Tokanai, Fuyuki

2015-01-01

Accelerator mass spectrometry (AMS) is expected to play an important role in microdose trials. In this study, we measured the "1"4C concentration in "1"4C-oxaliplatin-spiked serum, urine and supernatant of fecal homogenate samples in our Yamagata University (YU) – AMS system. The calibration curves of "1"4C concentration in serum, urine and supernatant of fecal homogenate were linear (the correlation coefficients were ⩾0.9893), and the precision and accuracy was within the acceptance criteria. To examine a "1"4C content of water in three vacuum blood collection tubes and a syringe were measured. "1"4C was not detected from water in these devices. The mean "1"4C content in urine samples of 6 healthy Japanese volunteers was 0.144 dpm/mL, and the intra-day fluctuation of "1"4C content in urine from a volunteer was little. The antineoplastic agents are administered to the patients in combination. Then, "1"4C contents of the antineoplastic agents were quantitated. "1"4C contents were different among 10 antineoplastic agents; "1"4C contents of paclitaxel injection and docetaxel hydrate injection were higher than those of the other injections. These results indicate that our quantitation method using YU-AMS system is suited for microdosing studies and that measurement of baseline and co-administered drugs might be necessary for the studies in low concentrations.

Accelerator mass spectrometry analysis of {sup 14}C-oxaliplatin concentrations in biological samples and {sup 14}C contents in biological samples and antineoplastic agents

Energy Technology Data Exchange (ETDEWEB)

Toyoguchi, Teiko, E-mail: tteiko@med.id.yamagata-u.ac.jp [Department of Pharmacy, Yamagata University Hospital, 2-2-2 Iida-Nishi, Yamagata-shi, Yamagata 990-9585 (Japan); Kobayashi, Takeshi; Konno, Noboru; Shiraishi, Tadashi [Department of Pharmacy, Yamagata University Hospital, 2-2-2 Iida-Nishi, Yamagata-shi, Yamagata 990-9585 (Japan); Kato, Kazuhiro; Tokanai, Fuyuki [Department of Physics, Faculty of Science, Yamagata University, 1-4-12 Kojirakawa-machi, Yamagata-shi, Yamagata 990-8560 (Japan)

2015-10-15

Accelerator mass spectrometry (AMS) is expected to play an important role in microdose trials. In this study, we measured the {sup 14}C concentration in {sup 14}C-oxaliplatin-spiked serum, urine and supernatant of fecal homogenate samples in our Yamagata University (YU) – AMS system. The calibration curves of {sup 14}C concentration in serum, urine and supernatant of fecal homogenate were linear (the correlation coefficients were ⩾0.9893), and the precision and accuracy was within the acceptance criteria. To examine a {sup 14}C content of water in three vacuum blood collection tubes and a syringe were measured. {sup 14}C was not detected from water in these devices. The mean {sup 14}C content in urine samples of 6 healthy Japanese volunteers was 0.144 dpm/mL, and the intra-day fluctuation of {sup 14}C content in urine from a volunteer was little. The antineoplastic agents are administered to the patients in combination. Then, {sup 14}C contents of the antineoplastic agents were quantitated. {sup 14}C contents were different among 10 antineoplastic agents; {sup 14}C contents of paclitaxel injection and docetaxel hydrate injection were higher than those of the other injections. These results indicate that our quantitation method using YU-AMS system is suited for microdosing studies and that measurement of baseline and co-administered drugs might be necessary for the studies in low concentrations.

Radioimmunoassay for chicken avidin. Comparison with a (/sup 14/C)biotin-binding method

Energy Technology Data Exchange (ETDEWEB)

Kulomaa, M S; Elo, H A; Tuohimaa, P J [Tampere Univ. of Tech. (Finland)

1978-11-01

A double-antibody solid-phase radioimmunoassay for chicken avidin is reported. Avidin was labelled with /sup 125/I by the chloramine-T method. The bound and free avidin were separated with a second antibody bound to a solid matrix. In the logit-log scale the standard curve was linear from 1-2 to 100-200ng of avidin/ml. Cross-reaction of ovalbumin was less than 0.015%. Saturation of biotin-binding sites of avidin with an excess of biotin decreased radioimmunoassay values by about 15%. Recovery studies indicated that avidin can be assayed from all chicken tissues studied with radioimmunoassay, whereas the (/sup 14/C)biotin/bentonite method gave poor recoveries for avidin in the liver and kidney. Radioimmunoassay and the (/sup 14/C)biotin/bentonite method gave similar concentrations for oviduct avidin.

The synthesis of Org 3770 labelled with 3H, 13C and 14C

International Nuclear Information System (INIS)

Kaspersen, F.M.; Rooij, F.A.M. van; Sperling, E.G.M.; Wieringa, J.H.

1989-01-01

The syntheses of 1,2,3,4,10,14b-hexahydro-2-methylpyrazino[2,1-a]pyrido[2,3-c][2]benazepine (Org 3770) labelled with 3 H (and 2 H), 13 C and 14 C are described. Tritiated Org 3770 was prepared either by exchange under alkaline conditions with tritiated water or catalytic reductive dehalogenation of a chloro analogue with 3 H 2 . 13 C-labelled material was obtained in a seven-step synthesis starting from 13 C-labelled benzene whereas 14 C-Org 3770 was prepared in a three-step synthesis starting with 14 CO 2 . All labelled compounds were analyzed by TLC, HPLC, MS and NMR. (author)

Metabolism of 14C-lindane in flooded alluvial soil

International Nuclear Information System (INIS)

Siddaramappa, R.; Sethunathan, N.

1975-01-01

The effect of rice straw on the persistence of uniformly ring labelled 14 C-lindane in an alluvial soil was investigated under flooded conditions. The residues in the soil were extracted with chloroform-diethyl ether and the radioactivity was measured by liquid scintillation. The radioactivity in the solvent phase decreased more rapidly in amended soil than in unamended soil. Radioautograph of thin layer chromatograms of solvent phase indicated that lindane was readily converted to a breakdown product in both amended and unamended soils. This breakdown product was also formed in both autoclaved and nonautoclaved soils. Rice straw amendment enhanced further decomposition of lindane and its breakdown product. Heat treatment retarded further decomposition of lindane and its breakdown product whereas they were rapidly decomposed in nonautoclaved soil. These studies indicated that in flooded alluvial soil tested, lindane was initially decomposed by a chemical reaction and soil microorganisms appeared to attack the products of the chemical reaction. (author)

Evaluation of [14C] and [13C]Sucrose as Blood-Brain Barrier Permeability Markers.

Science.gov (United States)

Miah, Mohammad K; Chowdhury, Ekram A; Bickel, Ulrich; Mehvar, Reza

2017-06-01

Nonspecific quantitation of [ 14 C]sucrose in blood and brain has been routinely used as a quantitative measure of the in vivo blood-brain barrier (BBB) integrity. However, the reported apparent brain uptake clearance (K in ) of the marker varies widely (∼100-fold). We investigated the accuracy of the use of the marker in comparison with a stable isotope of sucrose ([ 13 C]sucrose) measured by a specific liquid chromatography-tandem mass spectrometry method. Rats received single doses of each marker, and the K in values were determined. Surprisingly, the K in value of [ 13 C]sucrose was 6- to 7-fold lower than that of [ 14 C]sucrose. Chromatographic fractionation after in vivo administration of [ 14 C]sucrose indicated that the majority of the brain content of radioactivity belonged to compounds other than the intact [ 14 C]sucrose. However, mechanistic studies failed to reveal any substantial metabolism of the marker. The octanol:water partition coefficient of [ 14 C]sucrose was >2-fold higher than that of [ 13 C]sucrose, indicating the presence of lipid-soluble impurities in the [ 14 C]sucrose solution. Our data indicate that [ 14 C]sucrose overestimates the true BBB permeability to sucrose. We suggest that specific quantitation of the stable isotope ( 13 C) of sucrose is a more accurate alternative to the current widespread use of the radioactive sucrose as a BBB marker. Copyright © 2017 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.

Experimental Investigation of Phase Equilibria in the Ho-Ti-Si Ternary System at 973 K (700 °C)

Science.gov (United States)

Han, Feng; Zhan, Yongzhong

2018-02-01

Phase equilibrium relations of the Ho-Ti-Si ternary system at 973 K (700 °C) were experimentally researched by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive spectrometer (EDS). The isothermal section of the system at 973 K (700 °C) consists of 14 three-phase regions, 27 two-phase regions, and 14 single-phase regions. The phases Ti5Si3, Ti5Si4, TiSi, TiSi2, Ho5Si3, Ho5Si4, HoSi, αHoSi2-b, and βHoSi2-a are proved to exist at 973 K (700 °C). Previously reported HoTiSi and Ho2Ti3Si4 ternary compounds were confirmed to exist at this temperature. The solubility of Ho in the intermediate phases (i.e., TiSi2, TiSi, Ti5Si4, and Ti5Si3) at the Ti-Si side is extremely small. The maximum solubilities of Ti in HoSi2-b, Ho5Si4, and Ho5Si3 are confirmed to be 8.0, 7.2, and 6.0 at. pct, respectively.

Role of biotransformation, sorption and mineralization of (14)C-labelled sulfamethoxazole under different redox conditions.

Science.gov (United States)

Alvarino, T; Nastold, P; Suarez, S; Omil, F; Corvini, P F X; Bouju, H

2016-01-15

(14)C-sulfamethoxazole biotransformation, sorption and mineralization was studied with heterotrophic and autotrophic biomass under aerobic and anoxic conditions, as well as with anaerobic biomass. The (14)C-radiolabelled residues distribution in the solid, liquid and gas phases was closely monitored along a total incubation time of 190 h. Biotransformation was the main removal mechanism, mineralization and sorption remaining below 5% in all the cases, although the presence of a carbon source exerted a positive effect on the mineralization rate by the aerobic heterotrophic bacteria. In fact, an influence of the type of primary substrate and the redox potential was observed in all cases on the biotransformation and mineralization rates, since an enhancement of the removal rate was observed when an external carbon source was used as a primary substrate under aerobic conditions, while a negligible effect was observed under nitrifying conditions. In the liquid phases collected from all assays, up to three additional peaks corresponding to (14)C-radiolabelled residues were detected. The highest concentration was observed under anaerobic conditions, where two radioactive metabolites were detected representing each around 15% of the total applied radioactivity after 180 h incubation. One of the metabolites detected under anoxic and anaerobic conditions, is probably resulting from ring cleavage of the isoxazole ring. Copyright © 2015 Elsevier B.V. All rights reserved.

Autoradiography of [14C]paraquat or [14C]diquat in frogs and mice: accumulation in neuromelanin

International Nuclear Information System (INIS)

Lindquist, N.G.; Larsson, B.S.; Lyden-Sokolowski, A.

1988-01-01

The herbicide paraquat has been suggested as a causative agent for Parkinson's disease because of its structural similarity to a metabolite of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), which may induce a parkinsonism-like condition. MPTP as well as its metabolite 1-methyl-4-phenylpyridine have melanin affinity, and the parkinsonism-inducing potency of MPTP is much stronger in species with melanin in the nerve cells. Autoradiography of [ 3 H]MPTP in experimental animals has shown accumulation in melanin-containing tissues, including pigmented neurons. In the present whole body autoradiographic study accumulation and retention was seen in neuromelanin in frogs after i.p. injection of [ 14 C]paraquat or[ 14 C]diquat. By means of whole body autoradiography of [ 14 C]diquat in mice (a species with no or very limited amounts of neuromelanin) a low, relatively uniformly distributed level of radioactivity was observed in brain tissue. Accumulation of toxic chemical compounds, such as paraquat, in neuromelanin may ultimately cause lesions in the pigmented nerve cells, leading to Parkinson's disease

Sources of C-14 generation and associated doses

International Nuclear Information System (INIS)

Amado, Valeria A.; Biaggio, Alfredo L.; Canoba, Analia C.; Curti, Adriana R.

2009-01-01

C-14 is a radioactive isotope of C with a half-life of 5700 years that decays to N-14 by emission of beta radiation. It is naturally produced in the upper atmosphere by cosmic ray neutrons via the (n;p) reaction over N-14. Anthropogenic C-14 has been generated in the past by atmospheric nuclear weapon tests and it is currently produced during the operation of nuclear reactors. Once released this radionuclide behaves in the biosphere as the standard carbon cycle. Since the beginning of the industrial period the relationship Carbon-14/Stable Carbon has changed continuously, and so the dose incurred by the world population. In this paper the main anthropogenic activities that modified such relationship are presented and analyzed: the Suess effect and the generation of nuclear energy. It is concluded that the current trend of reduction of the total dose due to C-14 will continue during the next decades. Finally it is indicated that in order to prevent an excessive accumulation of this radionuclide in the biosphere, actions should be collectively implemented to be effective. (author) [es

Radiocarbon 14C differentiation of sparkling and carbonated wines

International Nuclear Information System (INIS)

Martin, G.E.; Krueger, H.W.; Burggraff, J.M.

1985-01-01

Specific 14 C-activities, percent of modern 14 C-activity, and calculated percent of fermentation CO 2 are presented for CO 2 contained in commercial sparkling wines, labeled as champagne or produced by the bulk (charmat) process. These data are given for the production years 1976-1982. The survey encompassed effervescent wines produced in Spain, Italy, West Germany, California, and New York. Addition of synthetic CO 2 to approximately 40 samples represented as sparkling wines was indicated by low 14 C-activities of CO 2 in these wines. Data for 14 C-activity were also presented for the ethanol distilled from sparkling wines for the years 1977-1980. In all cases, the 14 C-activity of ethanol was appropriate to the year of vintage

Changes in the level of [14C]indole-3-acetic acid and [14C]indoleacetylaspartic acid during root formation in mung bean cuttings

International Nuclear Information System (INIS)

Norcini, J.G.; Heuser, C.W.

1988-01-01

Changes in the levels of [ 14 C]indole-3-acetic acid (IAA) and [ 14 C]indoleacetylaspartic acid (IAAsp) were examined during adventitious root formation in mung bean (Vigna radiata [L.] R. Wilcz. Berken) stem cuttings. IAAsp was identified by GC-MS as the primary conjugate in IAA-treated cuttings. During root formation in IAA-treated cuttings, the level of [ 14 C]IAAsp increased rapidly the first day and then declined; [ 14 C]IAA was rapidly metabolized and not detected after 12 hours

Comparative in vitro metabolism of 1-14C-oleic acid and 1-14C-erucic acid in liver, heart and skeletal muscles of rats

International Nuclear Information System (INIS)

Bhatia, I.S.; Sharma, A.K.; Ahuja, S.P.

1978-01-01

In vitro oxidation of 14 C-oleic and 1- 14 C-erucic acid and their incorporation into lipids by liver, heart and skeletal muscles from female albino rats were studied. These tissues were obtained from rats maintained for 120 days on low fat diet or diets containing 15% mustard oil or 15% groundnut oil. In all these tissues from rats on different types of diets, the oxidation of 1- 14 C-erucic acid was lower than that 1- 14 C-oleic acid. There was little accumulation of lipids in heart after 120 days of feeding mustard oil. Oxidation of 1- 14 C-erucic acid was enhanced in liver, heart and skeletal muscles of rats conditioned to the mustard oil diet supplying erucic acid. Oxidation of erucic acid was maximum in liver and least in heart, whereas there were no differences in the oxidation of 1- 14 C-oleic acid in these tissues. Incorporation of 1- 14 C-oleic acid into triglycerides and phospholipids was not affected by the type of diet or tissues Incorporation of 1- 14 C-erucic acid was mainly into triglycerides of heart and skeletal muscles of rats not accustomed to mustard oil diet whereas these tissues from rats accustomed to mustard oil diets incorporated 1- 14 C-erucic acid both into the triglycerides and phospholipids. (author)

Investigations on diffusion-controlled transformations in creep resistant steels and graded cemented carbides

International Nuclear Information System (INIS)

Prat Borquez, Orlando

2011-01-01

The objective of this work was to simulate diffusion-controlled transformations on engineering alloys designed by the author and his colleagues. The main challenge of the work is to adapt the existing DICTRA models to the experimental processing and working conditions investigated, as well as to find the adequate boundary conditions for the description of the diffusion-controlled transformations governing the microstructure formation and evolution, in order to obtain reliable simulation results. The simulations were compared with experimental results of the microstructure evolution by scanning electron microscopy and scanning transmission electron microscopy (STEM). Two groups of materials were investigated. The first group was 9-12% Cr heat resistant alloys. These alloys are particularly interesting because the microstructure evolves during working conditions. Different compositions were designed in order to form different kinds and amounts of precipitates. For the designed 9-12% Cr creep steels the coarsening of MX and M 23 C 6 particles was modeled by applying the coarsening model implemented in DICTRA. The cell method of DICTRA was applied to investigate the kinetics of the Laves phase growth on 9-12% Cr alloys. The particular objectives of these investigations were: a) to determine the coarsening rate of precipitates, b) to investigate the influence of alloying element on the growth rate of the Laves phase, c) to determine the influence of the M 23 C 6 formation on the growth kinetics of the Laves phase, d) to determine the growth mechanism at the interface of the Laves phase (i.e. up-hill diffusion), e) to investigate the effect of the cell size on the simulation kinetics of Laves phase. The second group of materials was cemented carbides. They are used as cutting tools or wear parts in the automotive, aircraft and mining industry among others. The wear performance of cemented carbides (hardmetals and cermets) can be largely improved by applying wear

Correction procedures for C-14 dates

International Nuclear Information System (INIS)

McKerrell, H.

1975-01-01

There are two quite separate criteria to satisfy before accepting as valid the corrections to C-14 dates which have been indicated for some years now by the bristlecone pine calibration. Firstly the correction figures have to be based upon all the available tree-ring data and derived in a manner that is mathematically sound, and secondly the correction figures have to produce accurate results on C-14 dates from archaeological test samples of known historical date, these covering as wide a period as possible. Neither of these basic prerequisites has yet been fully met. Thus the two-fold purpose of this paper is to bring together, and to compare with an independently based procedure, the various correction curves or tables that have been published up to Spring 1974, as well as to detail the correction results on reliable, historically dated Egyptian, Helladic and Minoan test samples from 3100 B.C. The nomenclature followed is strictly that adopted by the primary dating journal Radiocarbon, all C-14 dates quoted thus relate to the 5568 year half-life and the standard AD/BC system. (author)

Application of AMS 14C measurements to criminal investigations

International Nuclear Information System (INIS)

Nakamura, T.; Ohta, T.; Nishida, M.; Ikeda, A.; Oda, H.; Kojima, S.; Niu, E.

2005-01-01

14 C variations of atmospheric CO 2 as well as carbonaceous materials of human body, such as collagen fractions from teeth and bone, tissue, hair, nail, etc., of modern humans dead or alive, are influenced by 14 C produced artificially by nuclear bomb tests in the atmosphere from late 1950s to early 1960s. By careful investigation of 14 C concentration of tree rings and human tissue samples formed in this time ranges, we can establish a relation between their 14 C concentrations and calendar year. By applying this relation to a sample whose 14 C concentration can be measured, we can estimate the formation age of the sample. In addition, sources of the drugs that were used in some criminal cases can be possibly identified by the analysis of their carbon isotope ratios ( 13 C/ 12 C and 14 C/ 12 C). This method of age determination was applied to a forensic study; i.e., to two similar cases of murder. One of the two cases is for a dead body of a modern human who was killed in 1978 and buried under the floor of the house owned by the murderer. The body was excavated in 2004 according to the confession by the murderer. 14 C abundances of several pieces of hair and one tooth (the third molar) from the body were measured with accelerator mass spectrometry (AMS), and compared with the annual change on concentrations of bomb-produced 14 C. The time of death of the body was estimated to be at around 1977, and her age was from 30 to 37 years old at that time. These estimations were consistent with the real values that were revealed after the case was solved by the confession of the real murderer who gave himself up to the police. For the other case, 14 C analysis was also consistent with the fact revealed by police investigations as well as by the confession of the real murderer.