Inner-shell excitation and ionic fragmentation of molecules

International Nuclear Information System (INIS)

Hitchcock, A.P.; Tyliszczak, T.; Cavell, R.G.

1997-01-01

Inner-shell excitation and associated decay spectroscopies are site specific probes of electronic and geometrical structure and photoionization dynamics. X-ray absorption probes the geometric and electronic structure, while time-of-flight mass spectrometry with multi-coincidence detection provides information on the photofragmentation dynamics of the initially produced inner-shell state. Auger decay of inner-shell excited and ionised states is an efficient source of multiply charged ions. The charge separation and fragmentation of these species, studied by photoelectron-photoion-photoion coincidence (also called charge separation mass spectrometry) gives insights into bonding and electronic structure. In molecules, the dependence of the fragmentation process on the X-ray energy can reveal cases of site and/or state selective fragmentation. At the ALS the authors have examined the soft X-ray spectroscopy and ionic fragmentation of a number of molecules, including carboranes, silylenes, phosphorus halides, SF 6 and CO 2 . Their work is illustrated using results from the carborane and PF 3 studies

Inner-shell excitation and ionic fragmentation of molecules

Energy Technology Data Exchange (ETDEWEB)

Hitchcock, A.P.; Tyliszczak, T. [McMaster Univ., Hamilton, Ontario (Canada); Cavell, R.G. [Univ. of Alberta, Edmonton (Canada)] [and others

1997-04-01

Inner-shell excitation and associated decay spectroscopies are site specific probes of electronic and geometrical structure and photoionization dynamics. X-ray absorption probes the geometric and electronic structure, while time-of-flight mass spectrometry with multi-coincidence detection provides information on the photofragmentation dynamics of the initially produced inner-shell state. Auger decay of inner-shell excited and ionised states is an efficient source of multiply charged ions. The charge separation and fragmentation of these species, studied by photoelectron-photoion-photoion coincidence (also called charge separation mass spectrometry) gives insights into bonding and electronic structure. In molecules, the dependence of the fragmentation process on the X-ray energy can reveal cases of site and/or state selective fragmentation. At the ALS the authors have examined the soft X-ray spectroscopy and ionic fragmentation of a number of molecules, including carboranes, silylenes, phosphorus halides, SF{sub 6} and CO{sub 2}. Their work is illustrated using results from the carborane and PF{sub 3} studies.

Inner-shell photoionization of group-IIB atoms

International Nuclear Information System (INIS)

Kutzner, M.; Tidwell, C.; Vance, S.E.; Radojevic, V.

1994-01-01

Total and partial photoionization cross sections, branching ratios, and angular-distribution asymmetry parameters for inner subshells (nl,l≥2) of the group-IIB elements zinc, cadmium, and mercury have been calculated in both the relativistic random-phase approximation and the relativistic random-phase approximation modified to include relaxation. Comparisons are made between the results of the two theoretical methods and with experiment where available. The present theoretical results for the 3d inner-shell photoionization of zinc are not in accord with experiment. We confirm previous work [S. L. Carter and H. P. Kelly, J. Phys. B 11, 2467 (1978)] which demonstrated that relaxation is an important effect in photoionization of the 4d subshell of atomic cadmium. It is also found that the inclusion of relaxation effects resolves a discrepancy between theory and experiment for the 4f inner-shell photoionization of atomic mercury

Impact parameter dependence of inner-shell ionization probabilities

International Nuclear Information System (INIS)

Cocke, C.L.

1974-01-01

The probability for ionization of an inner shell of a target atom by a heavy charged projectile is a sensitive function of the impact parameter characterizing the collision. This probability can be measured experimentally by detecting the x-ray resulting from radiative filling of the inner shell in coincidence with the projectile scattered at a determined angle, and by using the scattering angle to deduce the impact parameter. It is conjectured that the functional dependence of the ionization probability may be a more sensitive probe of the ionization mechanism than is a total cross section measurement. Experimental results for the K-shell ionization of both solid and gas targets by oxygen, carbon and fluorine projectiles in the MeV/amu energy range will be presented, and their use in illuminating the inelastic collision process discussed

Inner shell excitation in atoms and molecules by high resolution electron impact

International Nuclear Information System (INIS)

King, G.C.

1986-01-01

In this work an inner-shell spin-forbidden transition in N 2 and a parity-forbidden transition in Ar were studied. These transitions were observed by using incident electron energies as low as 1.15 times the excitation energy of the inner-shell states. (Auth.)

Interparticle interactions of FePt core and Fe{sub 3}O{sub 4} shell in FePt/Fe{sub 3}O{sub 4} magnetic nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Akbari, Hossein, E-mail: Akbari.ph@iauardabil.ac.ir [Department of Physics, Ardabil Branch, Islamic Azad University, Ardabil (Iran, Islamic Republic of); Zeynali, Hossein [Department of Physics, Kashan Branch, Islamic Azad University, Kashan (Iran, Islamic Republic of); Bakhshayeshi, Ali [Department of Physics, Mashhad Branch, Islamic Azad University, Mashhad (Iran, Islamic Republic of)

2016-02-22

Monodisperse FePt nanoparticles were successfully synthesized using simple wet chemical method. Fe{sub 3}O{sub 4} was used as a magnetic shell around each FePt nanoparticles. In FePt/Fe{sub 3}O{sub 4} core/shell system, core thickness is 2 nm and shell thickness varies from zero to 2.5 nm. A theoretical model presented to calculate the shell thickness dependence of Coercivity. Presented model is compared with the results from Stoner–Wohlfarth model to interpret the shell thickness dependence of Coercivity in FePt/Fe{sub 3}O{sub 4} core/shell nanoparticles. There is a difference between the results from Stoner–Wohlfarth model and experimental data when the shell thickness increases. In the presented model, the effects of interparticle exchange and random magneto crystalline anisotropy are added to the previous models of magnetization reversal for core/shell nanostructures in order to achieve a better agreement with experimental data. For magnetic shells in FePt/Fe{sub 3}O{sub 4} core/shell, effective coupling between particles increases with increasing shell thickness which leads to Coercivity destruction for stronger couplings. According to the boundary conditions, in the harder regions with higher exchange stiffness, there is small variation in magnetization and so the magnetization modes become more localized. We discussed both localized and non-localized magnetization modes. For non-zero shell thickness, non-localized modes propagate in the soft phase which effects the quality of particle exchange interactions. - Highlights: • Monodisperse FePt nanoparticles were successfully synthesized using simple wet chemical method. • Fe{sub 3}O{sub 4} was used as a magnetic shell around each FePt nanoparticles. • A theoretical model presented to calculate the shell thickness dependence of Coercivity. • Magnetic shells increase effective coupling between particles with increasing shell thickness. • Magnetization modes are more localized in the regions with

Development of Special Tools for the Straightness Measurement of JRTR Core Inner Shell

International Nuclear Information System (INIS)

Sinjlawi, Abdullah; Cho, Yeong-Garp; Chung, Jong-Ha

2014-01-01

Jordan Research and Training Reactor (JRTR) is an open pool type nuclear research reactor, 5 MW power, JRTR core made from Zircaloy. The JRTR will be used for nuclear applications such as isotopes production, nuclear researches, neutron transmutation doping (NTD), and training. JRTR core structures will be exposed to a large amount of neutron irradiation during the life time of the reactor. The core inner shell also will be exposed to a pressure that comes from heavy water system. JRTR core inner shell will deform due to the neutron irradiation and the mechanical stress. Therefore, the dimensional change of the core inner shell should be periodically (every 10 years) measured as an in-service inspection to confirm the structural integrity. As a result of neutron irradiation, pressure difference of the heavy water vessel, and the mechanical stress, the reactor core will deform as shown in figure 2 to figure 4. The maximum deformation to the normal direction of inner shell wall is 0.75 mm as shown in figure 3. This study discusses development of special tools that will be used for pre-service and in-service inspection of JRTR inner shell. The performance and procedure for the measurements tools will be verified using by the real inner shell of the heavy water vessel at factory before shipping to Jordan.. There will be very delicate working procedure for the measurement in the limited space in JRTR core. Therefore, we will develop the detail procedures to cover the removal of the core components, installation of the measurement tools, measurement, and re-installation of the core components. The measurement of the inner shell at JAEC site during commissioning stage will be the first remote measurement at the same conditions of pool water and heavy water system

Optimization of ship inner shell to improve the safety of seagoing transport ship

Directory of Open Access Journals (Sweden)

Yan-Yun YU

2013-09-01

Full Text Available A practical Ship Inner Shell Optimization Method (SISOM, the purpose of which is to improve the safety of the seagoing transport ship by decreasing the maximum Still Water Bending Moment (SWBM of the hull girder under all typical loading conditions, is presented in this paper. The objective of SISOM is to make the maximum SWBM minimum, and the section areas of the inner shell are taken as optimization variables. The main requirements of the ship performances, such as cargo hold capacity, propeller and rudder immersion, bridge visibility, damage stability and prevention of pollution etc., are taken as constraints. The penalty function method is used in SISOM to change the above nonlinear constraint problem into an unconstrained one, which is then solved by applying the steepest descent method. After optimization, the optimal section area distribution of the inner shell is obtained, and the shape of inner shell is adjusted according to the optimal section area. SISOM is applied to a product oil tanker and a bulk carrier, and the maximum SWBM of the two ships is significantly decreased by changing the shape of inner shell plate slightly. The two examples prove that SISOM is highly efficient and valuable to engineering practice.

Relativistic effects on inner-shell electron properties

International Nuclear Information System (INIS)

Desclaux, J.P.

1976-01-01

The influence of relativistic effects on hydrogen-like systems is first reviewed. After having considered one-electron systems, the influence of the other electrons is to be taken into account when considering inner ionization energy and ionization cross sections. Two-hole states in inner shells being then dealt with, the problem of angular momentum coupling among electrons can no longer be neglected. In an other way, this implies that wave functions are to be built on a jj basis instead of a ls one. Ksub(α)sup(h) hypersatellite spectra and KLL Auger transition energies are successively discussed

Electrochemical synthesis of CORE-shell magnetic nanowires

KAUST Repository

Ovejero, Jesús G.

2015-04-16

(Fe, Ni, CoFe) @ Au core-shell magnetic nanowires have been synthesized by optimized two-step potentiostatic electrodeposition inside self-assembled nanopores of anodic aluminium templates. The optimal electrochemical parameters (e.g., potential) have been firstly determined for the growth of continuous Au nanotubes at the inner wall of pores. Then, a magnetic core was synthesized inside the Au shells under suitable electrochemical conditions for a wide spectrum of single elements and alloy compositions (e.g., Fe, Ni and CoFe alloys). Novel opportunities offered by such nanowires are discussed particularly the magnetic behavior of (Fe, Ni, CoFe) @ Au core-shell nanowires was tested and compared with that of bare TM nanowires. These core-shell nanowires can be released from the template so, opening novel opportunities for biofunctionalization of individual nanowires.

Inner shells as a link between atomic and nuclear physics

International Nuclear Information System (INIS)

Merzbacher, E.

1982-01-01

Nuclear decay and reaction processes generally take place in neutral or partially ionized atoms. The effects of static nuclear properties (size, shape, moments) on atomic spectra are well known, as are electronic transitions accompanying nuclear transitions, e.g. K capture and internal conversion. Excitation or ionization of initially filled inner shells, really or virtually, may modify nuclear Q values, will require correction to measured beta-decay endpoint energies, and can permit the use of inner-shell transitions in the determination of nuclear widths. Improvements in resolution continue to enhance the importance of these effects. There is also beginning to appear experimental evidence of the dynamical effects of atomic electrons on the course of nuclear reactions. The dynamics of a nuclear reaction, which influences and may in turn be influenced by atomic electrons in inner shells, offers instructive examples of the interplay between strong and electromagnetic interactions and raises interesting questions about coherence properties of particle beams. A variety of significantly different collision regimes, depending on the atomic numbers of the collision partners and the collision velocity, will be discussed and illustrated. 21 References, 5 figures

A novel magnetic core-shell nanocomposite Fe3O4@chitosan@ZnO for the green synthesis of 2-benzimidazoles

Science.gov (United States)

Tian, Fei; Niu, Libo; Chen, Bo; Gao, Xuejia; Lan, Xingwang; Huo, Li; Bai, Guoyi

2017-10-01

A novel magnetic core-shell nanocomposite Fe3O4@Chitosan@ZnO was successfully prepared by in situ chemical precipitation method. It has a clear core-shell structure with magnetic Fe3O4 (about 160 nm in diameter) as core, chitosan as the inner shell, and ZnO as the outer shell, as demonstrated by the transmission electron microscopy and the related elemental mapping. Moreover, this nanocomposite has high magnetization (43.6 emu g-1) so that it can be easily separated from the reaction mixture within 4 s by an external magnetic field. The introduction of the natural chitosan shell, instead of the conventional SiO2 shell, and its combination with the active ZnO ensures this novel nanocomposite green character and good catalytic performance in the synthesis of 2-benzimidazoles with moderate to excellent isolated yields at room temperature. Notably, it can be recycled seven times without appreciable loss of its initial catalytic activity, demonstrating its good stability and making it an attractive candidate for the green synthesis of 2-benzimidazoles. [Figure not available: see fulltext.

Chemical and biological effects of β-decay and inner shell ionization in biomolecules

International Nuclear Information System (INIS)

Stoecklin, G.

1979-01-01

Tritium and iodine-125, and the Auger effect either caused by the EC-decay of 125 I or by the inner shell vacancy created selectively by mono-energetic X-ray are reviewed in this paper. The specifically labelled precursors to bound 3 H large biomolecules were prepared by conventional syntheses, and then incorporated into the DNA of proliferating cells. The effects like DNA strand breaks or mutational changes are likely to be affected by the localization of the carbonium ions in biological molecules. In contrast to lethality, it was demonstrated that 3 H transmutation effect contributed to DNA strand breaks and played a key role in producing genetic effects. The decay of 3 H in uracil-5- 3 H in the DNA of E. coli was about 7 times as mutagenic as that in uracil-6- 3 H, and 500-fold greater in bacteriophage S13. Drastic chemical consequences are associated with the Auger effect occurring as a possible relaxation process whenever inner shell ionization is initiated. When the vacancy is filled by an electron from an outer shell, the bond energy difference between inner shell electron and outer shell electron is released either in the form of an X-ray fluorescence photon or it can be transmitted to another outer electron which is then ejected. The radioactive decay in specifically labelled biomolecules or the inner shell ionization in heavy constituent atoms caused by resonant X-ray are relevant to a) selective microsurgery in biological macromolecules for the correlation of biological and chemical functions, b) radiotoxicity estimation, and c) radiation therapy. (Yamashita, S.)

Inner-shell electron spectroscopy for microanalysis

International Nuclear Information System (INIS)

Joy, D.C.; Maher, D.M.

1979-01-01

The transmission electron energy-loss spectrum shows characteristic edges corresponding to the excitation of inner-shell electrons of atoms in a thin sample. Analysis of these edges provides detailed chemical, structural, and electronic data from the radiated volume. By combining electron spectroscopy and electron microscopy, this microanalytical technique can be performed in conjunction with high-resolution imaging of the sample. It is shown that this approach has advantages of sensitivity, spatial resolution, and convenience over other comparable techniques. 7 figures

Multislice theory of fast electron scattering incorporating atomic inner-shell ionization

International Nuclear Information System (INIS)

Dwyer, C.

2005-01-01

It is demonstrated how atomic inner-shell ionization can be incorporated into a multislice theory of fast electron scattering. The resulting theory therefore accounts for both inelastic scattering due to inner-shell ionization and dynamical elastic scattering. The theory uses a description of the ionization process based on the angular momentum representation for both the initial and final states of the atomic electron. For energy losses near threshold, only a small number of independent states of the ejected atomic electron need to be considered, reducing demands on computing time, and eliminating the need for tabulated inelastic scattering factors. The theory is used to investigate the influence of the collection aperture size on the spatial origin of the silicon K-shell EELS signal generated by a STEM probe. The validity of a so-called local approximation is also considered

Profound Interfacial Effects in CoFe2O4/Fe3O4 and Fe3O4/CoFe2O4 Core/Shell Nanoparticles

Science.gov (United States)

Polishchuk, Dmytro; Nedelko, Natalia; Solopan, Sergii; Ślawska-Waniewska, Anna; Zamorskyi, Vladyslav; Tovstolytkin, Alexandr; Belous, Anatolii

2018-03-01

Two sets of core/shell magnetic nanoparticles, CoFe2O4/Fe3O4 and Fe3O4/CoFe2O4, with a fixed diameter of the core ( 4.1 and 6.3 nm for the former and latter sets, respectively) and thickness of shells up to 2.5 nm were synthesized from metal chlorides in a diethylene glycol solution. The nanoparticles were characterized by X-ray diffraction, transmission electron microscopy, and magnetic measurements. The analysis of the results of magnetic measurements shows that coating of magnetic nanoparticles with the shells results in two simultaneous effects: first, it modifies the parameters of the core-shell interface, and second, it makes the particles acquire combined features of the core and the shell. The first effect becomes especially prominent when the parameters of core and shell strongly differ from each other. The results obtained are useful for optimizing and tailoring the parameters of core/shell spinel ferrite magnetic nanoparticles for their use in various technological and biomedical applications.

Electrochemical performance and structure evolution of core-shell nano-ring α-Fe_2O_3@Carbon anodes for lithium-ion batteries

International Nuclear Information System (INIS)

Sun, Yan-Hui; Liu, Shan; Zhou, Feng-Chen; Nan, Jun-Min

2016-01-01

Core-shell nano-ring α-Fe_2O_3@Carbon (CSNR) composites with different carbon content (CSNR-5%C and CSNR-13%C) are synthesized using a hydrothermal method by controlling different amounts of glucose and α-Fe_2O_3 nano-rings with further annealing. The CSNR electrodes exhibit much improved specific capacity, cycling stability and rate capability compared with that of bare nano-ring α-Fe_2O_3 (BNR), which is attributed to the core-shell nano-ring structure of CSNR. The carbon shell in the inner and outer surface of CSNR composite can increase electron conductivity of the electrode and inhibit the volume change of α-Fe_2O_3 during discharge/charge processes, and the nano-ring structure of CSNR can buffer the volume change too. The CSNR-5%C electrode shows super high initial discharge/charge capacities of 1570/1220 mAh g"−"1 and retains 920/897 mAh g"−"1 after 200 cycles at 500 mA g"−"1 (0.5C). Even at 2000 mA g"−"1 (2C), the electrode delivers the initial capacities of 1400/900 mAh g"−"1, and still maintains 630/610 mAh g"−"1 after 200 cycles. The core-shell nano-rings opened during cycling and rebuilt a new flower-like structure consisting of α-Fe_2O_3@Carbon nano-sheets. The space among the nano-sheet networks can further buffer the volume expansion of α-Fe_2O_3 and facilitate the transportation of electrons and Li"+ ions during the charge/discharge processes, which increases the capacity and rate capability of the electrode. It is the first time that the evolution of core-shell α-Fe_2O_3@Carbon changing to flower-like networks during lithiation/de-lithiation has been reported.

Electrochemical performance and structure evolution of core-shell nano-ring α-Fe2O3@Carbon anodes for lithium-ion batteries

Science.gov (United States)

Sun, Yan-Hui; Liu, Shan; Zhou, Feng-Chen; Nan, Jun-Min

2016-12-01

Core-shell nano-ring α-Fe2O3@Carbon (CSNR) composites with different carbon content (CSNR-5%C and CSNR-13%C) are synthesized using a hydrothermal method by controlling different amounts of glucose and α-Fe2O3 nano-rings with further annealing. The CSNR electrodes exhibit much improved specific capacity, cycling stability and rate capability compared with that of bare nano-ring α-Fe2O3 (BNR), which is attributed to the core-shell nano-ring structure of CSNR. The carbon shell in the inner and outer surface of CSNR composite can increase electron conductivity of the electrode and inhibit the volume change of α-Fe2O3 during discharge/charge processes, and the nano-ring structure of CSNR can buffer the volume change too. The CSNR-5%C electrode shows super high initial discharge/charge capacities of 1570/1220 mAh g-1 and retains 920/897 mAh g-1 after 200 cycles at 500 mA g-1 (0.5C). Even at 2000 mA g-1 (2C), the electrode delivers the initial capacities of 1400/900 mAh g-1, and still maintains 630/610 mAh g-1 after 200 cycles. The core-shell nano-rings opened during cycling and rebuilt a new flower-like structure consisting of α-Fe2O3@Carbon nano-sheets. The space among the nano-sheet networks can further buffer the volume expansion of α-Fe2O3 and facilitate the transportation of electrons and Li+ ions during the charge/discharge processes, which increases the capacity and rate capability of the electrode. It is the first time that the evolution of core-shell α-Fe2O3@Carbon changing to flower-like networks during lithiation/de-lithiation has been reported.

Synthesis and characterization of ZnSe:Fe/ZnSe core/shell nanocrystals

Energy Technology Data Exchange (ETDEWEB)

Yang, Lin; Zhu, Jianguo, E-mail: yanglin_1028@163.com; Xiao, Dingquan

2014-04-15

High-quality ZnSe:Fe/ZnSe core/shell nanocrystals were prepared via a hydrothermal microemulsion technique. Effective surface passivation of monodisperse ZnSe:Fe nanocrystals is achieved by overcoating them with a ZnSe shell. The samples were characterized by means of XRD, EDX, TEM, PSD, XPS, photoluminescence, and Raman spectrum. The results show that the as-synthesized nanocrystals are cubic zinc blende ZnSe structure with high purity and the average particle size of ZnSe:Fe/ZnSe core/shell nanocrystal is larger than that of ZnSe:Fe core. The growth of ZnSe shell causes a small red shift in PL spectra, and then the PL quantum yield (QY) increases from 16% before shell growth to the maximum of 37% after increasing shell thickness up to 1.2 monolayers (ML). Moreover, both transverse optic (TO) and longitudinal optic (LO) phonon modes of ZnSe are shifted toward lower frequency as compared with the reported ones. -- Highlights: • ZnSe:Fe/ZnSe core/shell QDs were prepared by a hydrothermal microemulsion method. • ZnSe shell efficiently passivates surface defects by serving as a physical barrier. • The particle size and PL properties can be turned with the growth of ZnSe shell. • The luminescence efficiency and stability of QDs could be improved in this manner.

Inner-shell photodetachment from Ru-

International Nuclear Information System (INIS)

Dumitriu, I.; Gorczyca, T. W.; Berrah, N.; Bilodeau, R. C.; Pesic, Z. D.; Rolles, D.; Walter, C. W.; Gibson, N. D.

2010-01-01

Inner-shell photodetachment from Ru - was studied near and above the 4p excitation region, 29-to-91-eV photon energy range, using a merged ion-photon-beam technique. The absolute photodetachment cross sections of Ru - ([Kr]4d 7 5s 2 ) leading to Ru + , Ru 2+ , and Ru 3+ ion production were measured. In the near-threshold region, a Wigner s-wave law, including estimated postcollision interaction effects, locates the 4p 3/2 detachment threshold between 40.10 and 40.27 eV. Additionally, the Ru 2+ product spectrum provides evidence for simultaneous two-electron photodetachment (likely to the Ru + 4p 5 4d 6 5s 2 state) located near 49 eV. Resonance effects are observed due to interference between transitions of the 4p electrons to the quasibound 4p 5 4d 8 5s 2 states and the 4d→εf continuum. Despite the large number of possible terms resulting from the Ru - 4d open shell, the cross section obtained from a 51-state LS-coupled R-matrix calculation agrees qualitatively well with the experimental data.

Coercivity enhancement in Ce-Fe-B based magnets by core-shell grain structuring

Directory of Open Access Journals (Sweden)

M. Ito

2016-05-01

Full Text Available Ce-based R2Fe14B (R= rare-earth nano-structured permanent magnets consisting of (Ce,Nd2Fe14B core-shell grains separated by a non-magnetic grain boundary phase, in which the relative amount of Nd to Ce is higher in the shell of the magnetic grain than in its core, were fabricated by Nd-Cu infiltration into (Ce,Nd2Fe14B hot-deformed magnets. The coercivity values of infiltrated core-shell structured magnets are superior to those of as-hot-deformed magnets with the same overall Nd content. This is attributed to the higher value of magnetocrystalline anisotropy of the shell phase in the core-shell structured infiltrated magnets compared to the homogeneous R2Fe14B grains of the as-hot-deformed magnets, and to magnetic isolation of R2Fe14B grains by the infiltrated grain boundary phase. First order reversal curve (FORC diagrams suggest that the higher anisotropy shell suppresses initial magnetization reversal at the edges and corners of the R2Fe14B grains.

Study of magnetization and magnetoelectricity in CoFe2O4/BiFeO3 core-shell composites

Science.gov (United States)

Kuila, S.; Tiwary, Sweta; Sahoo, M. R.; Barik, A.; Babu, P. D.; Siruguri, V.; Birajdar, B.; Vishwakarma, P. N.

2018-02-01

CoFe2O4 (core)/BiFeO3 (shell) nanoparticles are prepared by varying the relative molar concentration of core and shell materials (40%CoFe2O4-60%BiFeO3, 50%CoFe2O4-50%BiFeO3, and 60%CoFe2O4-40%BiFeO3). The core-shell nature is confirmed from transmission electron microscopy on these samples. A plot of ΔM (=MFC-MZFC) vs temperature suggests the presence of two types of spin dynamics: (a) particle size dependent spin blocking and (b) spin-disorder. These two spin dynamic processes are found to contribute independently to the generation of magnetoelectric voltage. Very clear first order and second order magnetoelectric voltages are recorded. The resemblance of the first order magnetoelectric coefficient vs temperature plot to that of building up of order parameters in the mean field theory suggests that spin disorder can act like one of the essential ingredients in building the magnetoelectric coupling. The best result is obtained for the 50-50 composition sample, which may be due to better coupling of magnetostrictive CoFe2O4, and piezoelectric BiFeO3, because of the optimum thickness of shell and core.

A novel sandwich Fe-Mn damping alloy with ferrite shell prepared by vacuum annealing

Science.gov (United States)

Qian, Bingnan; Peng, Huabei; Wen, Yuhua

2018-04-01

To improve the corrosion resistance of high strength Fe-Mn damping alloys, we fabricated a novel sandwich Fe-17.5Mn damping alloy with Mn-depleted ferrite shell by vacuum annealing at 1100 °C. The formation behavior of the ferrite shell obeys the parabolic law for the vacuum annealed Fe-17.5Mn alloy at 1100 °C. The sandwich Fe-17.5Mn alloy with ferrite shell exhibits not only better corrosion resistance but also higher damping capacity than the conventional annealed Fe-17.5Mn alloy under argon atmosphere. The existence of only ferrite shell on the surface accounts for the better corrosion in the sandwich Fe-17.5Mn alloy. The better damping capacity in the sandwich Fe-17.5Mn alloy is owed to more stacking faults inside both ɛ martensite and γ austenite induced by the stress from ferrite shell. Vacuum annealing is a new way to improve the corrosion resistance and damping capacity of Fe-Mn damping alloys.

Excitation of the inner 4d shell of neutral iodine

Energy Technology Data Exchange (ETDEWEB)

Pettini, M; Tozzi, G P [Osservatorio Astrofisico di Arcetri, Florence (Italy); Mazzoni, M [Florence Univ. (Italy). Ist. di Astronomia

1981-03-23

The absorption spectrum of neutral atomic iodine has been photographed in the EUV region and three strong autoionized resonances have been identified. A broad absorption feature has been observed and is ascribed to a collective exitation of the 4d inner shell.

Calculation of Ion Charge State Distributions After Inner-Shell Ionization in Xe Atom

International Nuclear Information System (INIS)

Mohammedein, A.M.; Ghoneim, A.A.; Kandil, M.K.; Kadad, I.M.

2009-01-01

The vacancy cascades following initial inner-shell vacancies in single and multi-ionized atoms often lead to highly charged residual ions. The inner-shell vacancy produced by ionization processes may decay by either a radiative or non-radiative transition. In addition to the vacancy filling processes, there is an electron shake off process due to the change of core potential of the atom. In the calculation of vacancy cascades, the radiative (x-ray) and non-radiative (Auger and Coster-Kronig) branching ratios give valuable information on the de-excitation dynamics of an atom with inner-shell vacancy. The production of multi-charged ions yield by the Auger cascades following inner shell ionization of an atom has been studied both experimentally and theoretically. Multi-charged Xe ions following de-excitation of K, L 1 , L 2,3 , M 1 , M 2,3 and M 4,5 subshell vacancies are calculated using Monte-Carlo algorithm to simulate the vacancy cascade development. Fluorescence yield (radiative) and Auger, Coster- Kronig yield (non- radiative) are evaluated. The decay of K hole state through radiative transitions is found to be more probable than non-radiative transitions in the first step of de-excitation. On the other hand, the decay of L, M vacancies through non-radiative transitions are more probable. The K shell ionization in Xe atom mainly yields Xe 7+ , Xe 8+ , Xe 9+ and Xe 1 0 + ions, and the charged X 8+ ions are the highest. The main product from the L 1 shell ionization is found to be Xe 8+ , Xe 9+ ions, while the charged Xe 8+ ions predominate at L 2,3 hole states. The charged Xe 6+ , Xe 7+ and Xe 8+ ions mainly yield from 3s 1/2 and 3p 1/2 , 3/2 ionization, while Xe in 3d 3/2 , 5/2 hole states mainly turns into Xe 4+ and Xe 5+ ions. The present results are found to agree well with the experimental data. (author)

Autoionization of inner atomic shells during β decay

International Nuclear Information System (INIS)

Batkin, I.S.; Kopytin, I.V.; Smirnov, Y.G.; Churakova, T.A.

1981-01-01

A theory describing the autoionization of inner atomic shells in nuclear β decay has been developed. It is shown on the basis of diagram technique that in first order in Z -1 the matrix element of the process is represented in the form of the sum of two terms, one of which corresponds to ionization of an electron shell of an atom with sudden change of the charge of the nucleus, and the other to direct interaction of a β particle with the electrons of the atomic shell. Specific calculations are carried out in the nonrelativistic approximation with use of electron wave functions and a Green's function constructed with a Teitz screened Coulomb potential, the systematic inclusion of the contribution of the direct mechanism being carried out for the first time. For the case of β decay of the isotopes 35 S, 45 Ca, 63 Ni, 147 Pm, and 151 Sm we have calculated the shape of the spectrum of shakeup electrons and the integrated probability of autoionization of the K shell. It was found that the contribution of the direct mechanism in all cases considered is significant

Notes from the Nordic Spring Symposium on atomic inner shell phenomena

International Nuclear Information System (INIS)

Hansteen, J.M.; Gundersen, R.

1978-01-01

The purpose of the symposium was to bring together scientists from those various fields of physics that involve atomic inner shell processes. Vol. 2 contains the submitted complete lecture notes in chronological order. (JIW)

Dynamics of solid inner-shell electrons in collisions with bare and dressed swift ions

International Nuclear Information System (INIS)

Montanari, C.C.; Miraglia, J. E.; Arista, N.R.

2002-01-01

We analyze the dynamical interactions of swift heavy projectiles and solid inner-shell electrons. The dielectric formalism employed to deal with the free-electron gas is extended to account for the core electrons, by using the local plasma approximation. Results for stopping power, energy straggling, and inner-shell ionization in collisions of bare ions with metals are displayed, showing very good accord with the experimental data. Simultaneous excitations of projectile and target electrons are also analyzed. In the high-energy range we find a similar contribution of target core and valence electrons to the probability of projectile-electron loss. The problem of no excitation threshold within the local plasma approximation and the possibility of collective excitations of the shells are discussed

Fe Core–Carbon Shell Nanoparticles as Advanced MRI Contrast Enhancer

Directory of Open Access Journals (Sweden)

Rakesh P. Chaudhary

2017-10-01

Full Text Available The aim of this study is to fabricate a hybrid composite of iron (Fe core–carbon (C shell nanoparticles with enhanced magnetic properties for contrast enhancement in magnetic resonance imaging (MRI. These new classes of magnetic core–shell nanoparticles are synthesized using a one-step top–down approach through the electric plasma discharge generated in the cavitation field in organic solvents by an ultrasonic horn. Transmission electron microscopy (TEM observations revealed the core–shell nanoparticles with 10–85 nm in diameter with excellent dispersibility in water without any agglomeration. TEM showed the structural confirmation of Fe nanoparticles with body centered cubic (bcc crystal structure. Magnetic multi-functional hybrid composites of Fe core–C shell nanoparticles were then evaluated as negative MRI contrast agents, displaying remarkably high transverse relaxivity (r2 of 70 mM−1·S−1 at 7 T. This simple one-step synthesis procedure is highly versatile and produces desired nanoparticles with high efficacy as MRI contrast agents and potential utility in other biomedical applications.

Core-Shell Nano structure of a-Fe2O3/Fe3O4: Synthesis and Photo catalysis for Methyl Orange

International Nuclear Information System (INIS)

Tian, Y.; Wu, D.; Yu, B.; Jia, X.; Zhan, S.

2011-01-01

Fe 3 O 4 nanoparticle was synthesized in the solution involving water and ethanol. Then, a-Fe 2 O 3 shell was produced in situ on the surface of the Fe 3 O 4 nanoparticle by surface oxidation in molten salts, forming α-Fe 2 O 3 /Fe 3 O 4 core-shell nano structure. It was showed that the magnetic properties transformed from ferromagnetism to superparamagnetism after the primary Fe 3 O 4 nanoparticles were oxidized. Furthermore, the obtained a-Fe 2 O 3 /Fe 3 O 4 core-shell nanoparticles were used to photo catalyse solution of methyl orange, and the results revealed that a-Fe 2 O 3 /Fe 3 O 4 nanoparticles were more efficient than the self-prepared α-Fe 2 O 3 nanoparticles. At the same time, the photo catalyzer was recyclable by applying an appropriate magnetic field.

Synthesis and properties MFe2O4 (M = Fe, Co) nanoparticles and core-shell structures

Science.gov (United States)

Yelenich, O. V.; Solopan, S. O.; Greneche, J. M.; Belous, A. G.

2015-08-01

Individual Fe3-xO4 and CoFe2O4 nanoparticles, as well as Fe3-xO4/CoFe2O4 core/shell structures were synthesized by the method of co-precipitation from diethylene glycol solutions. Core/shell structure were synthesized with CoFe2O4-shell thickness of 1.0, 2.5 and 3.5 nm. X-ray diffraction patterns of individual nanoparticles and core/shell are similar and indicate that all synthesized samples have a cubic spinel structure. Compares Mössbauer studies of CoFe2O4, Fe3-xO4 nanoparticles indicate superparamagnetic properties at 300 K. It was shown that individual magnetite nanoparticles are transformed into maghemite through oxidation during the synthesis procedure, wherein the smallest nanoparticles are completely oxidized while a magnetite core does occur in the case of the largest nanoparticles. The Mössbauer spectra of core/shell nanoparticles with increasing CoFe2O4-shell thickness show a gradual decrease in the relative intensity of the quadrupole doublet and significant decrease of the mean isomer shift value at both RT and 77 K indicating a decrease of the superparamagnetic relaxation phenomena. Specific loss power for the prepared ferrofluids was experimentally calculated and it was determined that under influence of ac-magnetic field magnetic fluid based on individual CoFe2O4 and Fe3-xO4 particles are characterized by very low heating temperature, when magnetic fluids based on core/shell nanoparticles demonstrate higher heating effect.

Facile synthesis of flower like FePt@ZnO core–shell structure and its bifunctional properties

Energy Technology Data Exchange (ETDEWEB)

Majeed, Jerina [Chemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India); Jayakumar, O.D., E-mail: ddjaya@barc.gov.in [Chemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India); Mandal, B.P. [Chemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India); Salunke, H.G. [Technical Physics Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India); Naik, R. [Department of Physics, Wayne State University, Detroit, MI 48202 (United States); Tyagi, A.K., E-mail: aktyagi@barc.gov.in [Chemistry Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India)

2014-06-01

Graphical abstract: Flower shaped FePt and ZnO coated FePt with core–shell nanostructures are synthesized by a facile solvothermal procedure. Shell thickness of ZnO over FePt core was tuned by varying FePt concentration with respect to ZnO. Hybrid structure with lower FePt concentration exhibited bifunctionality such as near room temperature ferromagnetism and photoluminescence. Pristine FePt crystallize in the fct (L1{sub 0}) phase whereas it converts into fcc phase in presence of ZnO. - Highlights: • FePt@ZnO hybrid core–shell particles, with unique flower shape morphology have been prepared by solvothermal method. • Phase transition of fct-FePt to fcc-FePt has been found in presence of ZnO nanoparticles. • Plausible mechanism for growth of flowershaped nanoparticle is in accordance with energy minimization principle. • The core shell structure (FePt@ZnO) exhibits bi-functional properties. - Abstract: Flower shaped FePt and ZnO coated FePt (FePt@ZnO) core–shell nanostructures are synthesized by a facile solvothermal procedure. Two different compositions (molar ratio) of FePt and ZnO (FePt:ZnO = 1:3 and FePt:ZnO = 1:6) core–shells with different thicknesses of ZnO shells were synthesized. Hybrid FePt@ZnO core–shell flower structure with lower FePt concentration (FePt:ZnO = 1:6) exhibited bifunctionality including near room temperature ferromagnetism and photoluminescence at ambient conditions. X-ray diffraction patterns of pristine FePt showed partially ordered face centred tetragonal (fct) L1{sub 0} phase whereas ZnO coated FePt (FePt@ZnO) nanostructures showed hexagonal ZnO and disordered phase of FePt with fcc structure. The phase transition of fct FePt to fcc phase occurring in presence of ZnO is further confirmed by transmission electron microscopy and magnetic measurement studies. The formation of the nanoflowers was possibly due to growth along the [0 1 1] or [0 0 1] direction, keeping the core nearly spherical in accordance with the

Characterizing inner-shell with spectral phase interferometry for direct electric-field reconstruction

Science.gov (United States)

Mashiko, Hiroki; Yamaguchi, Tomohiko; Oguri, Katsuya; Suda, Akira; Gotoh, Hideki

2014-01-01

In many atomic, molecular and solid systems, Lorentzian and Fano profiles are commonly observed in a broad research fields throughout a variety of spectroscopies. As the profile structure is related to the phase of the time-dependent dipole moment, it plays an important role in the study of quantum properties. Here we determine the dipole phase in the inner-shell transition using spectral phase interferometry for direct electric-field reconstruction (SPIDER) with isolated attosecond pulses (IAPs). In addition, we propose a scheme for pulse generation and compression by manipulating the inner-shell transition. The electromagnetic radiation generated by the transition is temporally compressed to a few femtoseconds in the extreme ultraviolet (XUV) region. The proposed pulse-compression scheme may provide an alternative route to producing attosecond pulses of light. PMID:25510971

Recent advances in the synthesis of Fe3O4@AU core/shell nanoparticles

International Nuclear Information System (INIS)

Salihov, Sergei V.; Ivanenkov, Yan A.; Krechetov, Sergei P.; Veselov, Mark S.; Sviridenkova, Natalia V.; Savchenko, Alexander G.; Klyachko, Natalya L.; Golovin, Yury I.; Chufarova, Nina V.; Beloglazkina, Elena K.; Majouga, Alexander G.

2015-01-01

Fe 3 O 4 @Au core/shell nanoparticles have unique magnetic and optical properties. These nanoparticles are used for biomedical applications, such as magnetic resonance imaging, photothermal therapy, controlled drug delivery, protein separation, biosensors, DNA detection, and immunosensors. In this review, recent methods for the synthesis of core/shell nanoparticles are discussed. We divided all of the synthetic methods in two groups: methods of synthesis of bi-layer structures and methods of synthesis of multilayer composite structures. The latter methods have a layer of “glue” material between the core and the shell. - Highlights: • Fe 3 O 4 nanoparticles are promising for biomedical applications but have some disadvantages. • Covering Fe 3 O 4 nanoparticles with Au shell leads to better stability and biocompatibility. • Core/shell nanoparticles are widely used for biomedical applications. • There are two types of Fe 3 O 4 @Au core/shell nanoparticles structures: bi-layer and multilayer composite. • Different synthetic methods enable production of nanoparticles of different sizes

Electrochemical performance and structure evolution of core-shell nano-ring α-Fe{sub 2}O{sub 3}@Carbon anodes for lithium-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Sun, Yan-Hui, E-mail: sunyanhui0102@163.com; Liu, Shan; Zhou, Feng-Chen; Nan, Jun-Min

2016-12-30

Core-shell nano-ring α-Fe{sub 2}O{sub 3}@Carbon (CSNR) composites with different carbon content (CSNR-5%C and CSNR-13%C) are synthesized using a hydrothermal method by controlling different amounts of glucose and α-Fe{sub 2}O{sub 3} nano-rings with further annealing. The CSNR electrodes exhibit much improved specific capacity, cycling stability and rate capability compared with that of bare nano-ring α-Fe{sub 2}O{sub 3} (BNR), which is attributed to the core-shell nano-ring structure of CSNR. The carbon shell in the inner and outer surface of CSNR composite can increase electron conductivity of the electrode and inhibit the volume change of α-Fe{sub 2}O{sub 3} during discharge/charge processes, and the nano-ring structure of CSNR can buffer the volume change too. The CSNR-5%C electrode shows super high initial discharge/charge capacities of 1570/1220 mAh g{sup −1} and retains 920/897 mAh g{sup −1} after 200 cycles at 500 mA g{sup −1} (0.5C). Even at 2000 mA g{sup −1} (2C), the electrode delivers the initial capacities of 1400/900 mAh g{sup −1}, and still maintains 630/610 mAh g{sup −1} after 200 cycles. The core-shell nano-rings opened during cycling and rebuilt a new flower-like structure consisting of α-Fe{sub 2}O{sub 3}@Carbon nano-sheets. The space among the nano-sheet networks can further buffer the volume expansion of α-Fe{sub 2}O{sub 3} and facilitate the transportation of electrons and Li{sup +} ions during the charge/discharge processes, which increases the capacity and rate capability of the electrode. It is the first time that the evolution of core-shell α-Fe{sub 2}O{sub 3}@Carbon changing to flower-like networks during lithiation/de-lithiation has been reported.

Synthesis of double-shelled sea urchin-like yolk-shell Fe3O4/TiO2/Au microspheres and their catalytic applications

International Nuclear Information System (INIS)

Li, Jie; Tan, Li; Wang, Ge; Yang, Mu

2015-01-01

Double-shelled sea urchin-like yolk-shell Fe 3 O 4 /TiO 2 /Au microspheres were successfully synthesized through loading Au nanoparticles on the Fe 3 O 4 /TiO 2 support by a in situ reduction of HAuCl 4 with NaBH 4 aqueous solution. These microspheres possess tunable cavity size, adjustable shell layers, high structural stability and large specific surface area. The Au nanoparticles of approximately 5 nm in diameter were loaded both on the TiO 2 nanofibers and inside the cavities of sea urchin-like yolk-shell Fe 3 O 4 /TiO 2 microspheres. The sea urchin-like structure composed of TiO 2 nanofibers ensure the good distribution of the Au nanoparticles, while the novel double-shelled yolk-shell structure guarantees the high stability of the Au nanoparticles. Furthermore, the Fe 3 O 4 magnetic core facilitates the convenient recovery of the catalyst by applying an external magnetic field. The Fe 3 O 4 /TiO 2 /Au microspheres display excellent activities and recycling properties in the catalytic reduction of 4-nitrophenol (4-NP): the rate constant is 1.84 min −1 and turnover frequency is 5457 h −1 . (paper)

Inner shell transitions of BrI in the EUV

Energy Technology Data Exchange (ETDEWEB)

Mazzoni, M [Florence Univ. (Italy). Ist. di Astronomia; Pettini, M [Osservatorio Astrofisico di Arcetri, Florence (Italy)

1981-10-12

The EUV line spectrum originating from transitions of the inner 3d shell of neutral atomic bromine has been observed in absorption. Fano parameters have been derived for the three autoionized resonances nd/sup 10/(n + 1)s/sup 2/(n + 1)p/sup 5/ /sup 2/P-nd/sup 9/(n + 1)s/sup 2/(n + 1)p/sup 62/D observed in both bromine (n = 3) and iodine (n = 4) spectra.

Wavefunction effects in inner shell ionization of light atoms by protons

International Nuclear Information System (INIS)

Aashamar, K.; Amundsen, P.A.

An efficient computer code for calculating the impact parameter distribution of atomic ionization probabilities caused by charged particle impact, has been developed. The programme is based on the semiclassical approximation, and it allows the use of an arbitrary atomic central potential for deriving the one-electron orbitals that form the basis for the description of the atomic states. Extensive calculations are reported for proton induced K-shell ionization in carbon and neon, covering energies in the range 0.1-10 MeV. Some calculations on proton-argon L-shell ionization are also reported. Comparison of the results obtained using (screened) hydrogenic potentials and the recently reported energy- optimized effective atomic central potentials, respectively demonstrates that wavefunction effects are generally important for inner-shell ionization of light atoms. The agreement between theory and experiment in the K-shell case is improved for fast collisions upon using better wavefunctions. (Auth.)

High-resolution inner-shell spectroscopies of free atoms and molecules using soft-x-ray beamlines at the third-generation synchrotron radiation sources

International Nuclear Information System (INIS)

Ueda, Kiyoshi

2003-01-01

This article reviews the current status of inner-shell spectroscopies of free atoms and molecules using high-resolution soft-x-ray monochromators installed in the soft-x-ray beamlines at the third-generation synchrotron radiation facilities. Beamlines and endstations devoted to atomic and molecular inner-shell spectroscopies and various types of experimental techniques, such as ion yield spectroscopy, resonant photoemission spectroscopy and multiple-coincidence momentum imaging, are described. Experimental results for K-shell excitation of Ne, O K-shell excitation of H 2 O and CO 2 , C K-shell excitation and ionization of CO 2 and B K-shell excitation of BF 3 , obtained at beamline 27SU of SPring-8 in Japan, are discussed as examples of atomic and molecular inner-shell spectroscopies using the third-generation synchrotron radiation sources. (topical review)

Inner shell Coulomb ionization by heavy charged particles studied by the SCA model

International Nuclear Information System (INIS)

Hansteen, J.M.

1976-12-01

The seven papers, introduced by the most recent, subtitled 'A condensed status review', form a survey of the work by the author and his colleagues on K-, L-, and M-shell ionisation by impinging protons, deuterons and α-particles in the period 1971-1976. The SCA model is discussed and compared with other approximations for inner shell Coulomb ionisation. The future aspects in this field are also discussed. (JIW)

Deflection effects and charge transfer in inner-shell vacancy production

International Nuclear Information System (INIS)

Swafford, G.L.

1978-01-01

A method used in the calculation of inner shell ionization in asymmetric ion-atom collisions is extended to include projectile deflection effects and charge transfer to the projectile. Work is done in an independent electron model (Hartree-Fock) for the target, and the interaction is treated with the projectile as a time-dependent perturbation of the system. It is shown tht the time-dependent problem can be solved for the projectile moving along the classical hyperbolic trajectory that results from the nuclear repulsion. The method is very efficient due to the utilization the target-centered expansion of the system wave function. This means that all the required matrix elements can be pretabulated and are then available for use at all impact parameters. The method is first applied to the impact-parameter dependence of K-shell ionization by protons incident upon copper in the energy range 0.5 to 2 MeV. Excellent agreement with the experiments of Andersen et al., is found at the lower energy. Less satisfactory agreement is obtained in the higher energy region. Next the projectile is considered to move in a straight line path with constant velocity, and extend the method to include charge transfer between the target inner shells and the K-shell of the projectile. A critical feature of the results is the recognition of the importance of target continuum states of energy approximately equal to the kinetic energy (in the target frame) of the electron on the projectile. An approach is developed to properly include such resonance states in our pseudostate calculation. Selected numerical results are presented to illustrate the method and to demonstrate the projectile energy and nuclear charge dependence of the charge transfer cross sections

Structural and magnetic properties of CoFe{sub 2}O{sub 4}/NiFe{sub 2}O{sub 4} core/shell nanocomposite prepared by the hydrothermal method

Energy Technology Data Exchange (ETDEWEB)

Sattar, A.A. [Department of Physics, Faculty of Science, Ain Shams University, 11566 Abbasia, Cairo (Egypt); EL-Sayed, H.M., E-mail: h_m_elsaid@hotmail.com [Department of Physics, Faculty of Science, Ain Shams University, 11566 Abbasia, Cairo (Egypt); ALsuqia, Ibrahim [Department of Physics, Faculty of Education and Applied Science, Hajjah University, Alshahli, Hajjah (Yemen)

2015-12-01

CoFe{sub 2}O{sub 4}/NiFe{sub 2}O{sub 4} core/shell magnetic nanocomposite was synthesized by using hydrothermal method.The analysis of XRD indicated the coexistence of CoFe{sub 2}O{sub 4}, NiFe{sub 2}O{sub 4}as core/shell composite. The core/shell structure of the composite sample has been confirmed by HR-TEM images, EDX and FT-IR measurements. The size of obtained core/shell nanoparticles was 17 nm in core diameter and about 3 nm in shell thickness. The magnetization measurements showed that both the coercive field and the saturation magnetization of the resulting core/shell nanocomposite were slightly decreased compared to those of the CoFe{sub 2}O{sub 4} core but the thermal stability is of the magnetization parameter was enhanced. Furthermore, superparamagnetic phase is established at temperatures higher than the room temperature. The results were discussed in terms of the surface pinning and the magnetic interaction at the interface between the core and shell. - Highlights: • CoFe{sub 2}O{sub 4}/NiFe{sub 2}O{sub 4} core/shell could be prepared by hydrothermal method. • The structural analysis proved the formation of NiFe{sub 2}O{sub 4} shell with thickness 3 nm. • The thermal stability of M{sub s} and H{sub c} is enhanced due to the presence of NiFe{sub 2}O{sub 4} as a shell. • Super paramagnetic transition is confirmed and the effective magnetic anisotropy was calculated.

An efficient, selective collisional ejection mechanism for inner-shell population inversion in laser-driven plasmas

Energy Technology Data Exchange (ETDEWEB)

SCHROEDER,W. ANDREAS; NELSON,THOMAS R.; BORISOV,A.B.; LONGWORTH,J.W.; BOYER,K.; RHODES,C.K.

2000-06-07

A theoretical analysis of laser-driven collisional ejection of inner-shell electrons is presented to explain the previously observed anomalous kilovolt L-shell x-ray emission spectra from atomic Xe cluster targets excited by intense sub-picosecond 248nrn ultraviolet radiation. For incident ponderomotively-driven electrons photoionized by strong above threshold ionization, the collisional ejection mechanism is shown to be highly l-state and significantly n-state (i.e. radially) selective for time periods shorter than the collisional dephasing time of the photoionized electronic wavefunction. The resulting preference for the collisional ejection of 2p electrons by an ionized 4p state produces the measured anomalous Xe(L) emission which contains direct evidence for (i) the generation of Xe{sup 27+}(2p{sup 5}3d{sup 10}) and Xe{sup 28+}(2p{sup 5}3d{sup 9}) ions exhibiting inner-shell population inversion and (ii) a coherent correlated electron state collision responsible for the production of double 2p vacancies. For longer time periods, the selectivity of this coherent impact ionization mechanism is rapidly reduced by the combined effects of intrinsic quantum mechanical spreading and dephasing--in agreement with the experimentally observed and extremely strong {minus}{lambda}{sup {minus}6} pump-laser wavelength dependence of the efficiency of inner-shell (2p) vacancy production in Xe clusters excited in underdense plasmas.

Fabrication of Fe3O4@CuO core-shell from MOF based materials and its antibacterial activity

International Nuclear Information System (INIS)

Rajabi, S.K.; Sohrabnezhad, Sh.; Ghafourian, S.

2016-01-01

Magnetic Fe 3 O 4 @CuO nanocomposite with a core/shell structure was successfully synthesized via direct calcinations of magnetic Fe 3 O 4 @HKUST-1 in air atmosphere. The morphology, structure, magnetic and porous properties of the as-synthesized nano composites were characterized by using scanning electron microscope (SEM), transmission electron microscopy (TEM), powder X-ray diffraction (PXRD), and vibration sample magnetometer (VSM). The results showed that the nanocomposite material included a Fe 3 O 4 core and a CuO shell. The Fe 3 O 4 @CuO core-shell can be separated easily from the medium by a small magnet. The antibacterial activity of Fe 3 O 4 -CuO core-shell was investigated against gram-positive and gram-negative bacteria. A new mechanism was proposed for inactivation of bacteria over the prepared sample. It was demonstrated that the core-shell exhibit recyclable antibacterial activity, acting as an ideal long-acting antibacterial agent. - Graphical abstract: Fe 3 O 4 @CuO core-shell release of copper ions. These Cu 2+ ions were responsible for the exhibited antibacterial activity. - Highlights: • The Fe 3 O 4 @CuO core-shell was prepared by MOF method. • This is the first study of antibacterial activity of core-shell consist of CuO and Fe 3 O 4 . • The core-shell can be reused effectively. • Core-shell was separated from the reaction solution by external magnetic field.

Expansion connection of socket in flow distributed cabin of heavy water research reactor inner shell

International Nuclear Information System (INIS)

Jiang Zhiliang; Li Yanshui

1995-01-01

Expansion connection of aluminium alloy LT21 socket in flow distributed cabin of Heavy Water Research Reactor (HWRR) inner shell is described systematically. The expansion connection technology parameters of products are determined through tests. They are as following: bounce value of inner diameter after expansion, expansion degree, space between socket and plate hole, device for expanding pipes, selection of tools for enlarging or reaming holes, manufacture for socket inner hole and cleaning after expansion

Two step synthesis, electromagnetic and microwave absorbing properties of FeCo@C core–shell nanostructure

Energy Technology Data Exchange (ETDEWEB)

Afghahi, S.S.S., E-mail: salmanafghahi@gmail.com [Materials Science and Engineering Imam Hossein University, Department of Engineering, Babaei Highway, P.O. Box: 15816-18711, Tehran (Iran, Islamic Republic of); Shokuhfar, A. [Advanced Materials and Nanotechnology Research Laboratory, Department of Materials Science and Engineering K.N. Toosi University of Technology, P.O. Box: 19395-1999, Tehran (Iran, Islamic Republic of)

2014-12-15

In this research synthesis of FeCo@C core–shell nanoparticles was done using a novel two step process including the microemulsion technique and alcohol catalytic chemical vapor deposition. X-ray diffraction, transmission electron microscopy, electron beam diffraction and energy dispersive spectroscopy confirm the formation of FeCo@graphite core–shell nanostructure. Compared with FeCo nanoparticles with an oxide shell, the graphite shell restricts the growth of the FeCo nanoparticles, leading to lower saturation magnetization and higher natural-resonance frequency. The electromagnetic characteristics including permittivity, permeability and loss tangents of FeCo nanoparticles/nanoencapsulates were determined in the frequency range of 2–18 GHz. Results show that the graphite coating dramatically improves electromagnetic wave absorption of FeCo nanoparticles due to several dielectric/magnetic loss mechanisms. The main mechanism enhancing the dielectric loss tangent is Deby's dual relaxation phenomenon and for magnetic loss is the ferromagnetic resonance. The maximum reflection loss of −40 dB at 2.5 mm thickness and the maximum effective absorption bandwidth (RL<−20 dB) of 5.6 GHz at 3 mm thickness were obtained for FeCo nanoencapsulates. - Highlights: • FeCo@C core–shell nanoparticles were synthesized using a novel two step process. • Graphite coating dramatically improves the EM wave absorption of FeCo NPs. • FeCo@C nanoparticles represent high values of both magnetic and dielectric losses. • Maximum RL of −40 dB was obtained at 2.5 mm thickness. • Maximum effective bandwidth (RL<−20 dB) of 5.6 GHz was obtained at 3 mm thickness.

(FeCo)3Si-SiOx core-shell nanoparticles fabricated in the gas phase

International Nuclear Information System (INIS)

Bai Jianmin; Xu Yunhao; Thomas, John; Wang Jianping

2007-01-01

A method of fabricating core-shell nanoparticles by using an integrated nanoparticle deposition technique in the gas phase is reported. The principle of the method is based on nanoparticle growth from the vapour phase, during which elements showing lower surface energies prefer to form the shells and elements showing higher surface energies prefer to stay in the cores. This method was applied successfully to the Fe-Co-Si ternary system to fabricate core-shell-type nanoparticles. The nanoparticles were exposed in air after collection to achieve oxidation. The analysis results based on transmission electron microscopy (TEM), Auger electron spectroscopy (AES), x-ray diffraction (XRD), and a superconducting quantum interference device (SQUID) showed that the core parts are magnetic materials of body-centred cubic (bcc) structured (FeCo) 3 Si of 15 nm in diameter, and the shell parts are amorphous SiO x of 2 nm in thickness. These core-shell-type nanoparticles show a magnetic anisotropy constant of about 7 x 10 5 erg cm -3 and a saturation magnetization of around 1160 emu cm -3 , which is much higher than that of iron oxide. After annealing at 300 deg. C in air (FeCo) 3 Si-SiO x core-shell-type nanoparticles showed a little bit of a drop in magnetic moment, while pure FeCo nanopariticles totally lost their magnetic moment. This means that the shells of SiO x are dense enough to prevent the magnetic cores from oxidation

Synthesis of Pd-coated FeCo@Fe/C core-shell nanoparticles: microwave-induced ‘top-down’ nanostructuring and decoration

CSIR Research Space (South Africa)

Fashedemi, OO

2013-01-01

Full Text Available We report a novel microwave-induced fast and efficient synthesis of sub-10 nm sized palladium-decorated FeCo@Fe core–shell nanoparticles (ca. 3–7 nm) from a large-sized FeCo@Fe (0.21–1.5 µm) precursor, suggesting ‘top-down’ nanosizing. The high...

Ne, Ar, Fe, and Cu Auger-electron production at National Synchrotron Light Source

International Nuclear Information System (INIS)

Lee, D.H.; Johnson, B.M.; Jones, K.W.; Guardala, N.A.; Price, J.L.; Stumborg, M.F.; Glass, G.A.

1992-01-01

Energetic K and L Auger electrons produced by focussed, filtered, broad-band synchrotron radiation have been measured at the x-ray ring of the National Synchrotron Light Source (NSLS). The x-ray beam was used to study inner-shell photoionization of Ne and Ar gas and Fe and Cu solid film targets. The Auger electrons were analyzed by means of a semi-hemispherical electrostatic electron spectrometer at the energy resolution of ∼ 3 %. The electrons were detected at both 90 degree and 0 degree with respect to the photon beam direction. Broad distributions of the inner-shell photoelectrons were also observed, reflecting the incoming photon flux distribution. The Fe and Cu K Auger electron spectra were found to be very similar to the Ar K Auger electron spectra. This was expected, since deep inner-shell Auger processes are not affected by the outer valence electrons. Above 3 keV in electron energy, there have been few previous Auger electron measurements. 2 figs., 13 refs

Mössbauer Studies of Core-Shell FeO/Fe3O4 Nanoparticles

Science.gov (United States)

Kamzin, A. S.; Valiullin, A. A.; Khurshid, H.; Nemati, Z.; Srikanth, H.; Phan, M. H.

2018-02-01

FeO/Fe3O4 nanoparticles were synthesized by thermal decomposition. Electron microscopy revealed that these nanoparticles were of the core-shell type and had a spherical shape with an average size of 20 nm. It was found that the obtained FeO/Fe3O4 nanoparticles had exchange coupling. The effect of anisotropy on the efficiency of heating (hyperthermic effect) of FeO/Fe3O4 nanoparticles by an external alternating magnetic field was examined. The specific absorption rate (SAR) of the studied nanoparticles was 135 W/g in the experiment with an external alternating magnetic field with a strength of 600 Oe and a frequency of 310 kHz. These data led to an important insight: the saturation magnetization is not the only factor governing the SAR, and the efficiency of heating of magnetic FeO/Fe3O4 nanoparticles may be increased by enhancing the effective anisotropy. Mössbauer spectroscopy of the phase composition of the synthesized nanoparticles clearly revealed the simultaneous presence of three phases: magnetite Fe3O4, maghemite γ-Fe2O3, and wustite FeO.

Recent advances in the synthesis of Fe{sub 3}O{sub 4}@AU core/shell nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Salihov, Sergei V. [National University of Science and Technology MISiS, Leninskiy, Building 9, Moscow, 119049, Russian Federation, (Russian Federation); Ivanenkov, Yan A.; Krechetov, Sergei P.; Veselov, Mark S. [Moscow Institute of Physics and Technology (State University), 9 Institutskiy lane, Dolgoprudny City, Moscow Region, 141700 (Russian Federation); Sviridenkova, Natalia V.; Savchenko, Alexander G. [National University of Science and Technology MISiS, Leninskiy, Building 9, Moscow, 119049, Russian Federation, (Russian Federation); Klyachko, Natalya L. [National University of Science and Technology MISiS, Leninskiy, Building 9, Moscow, 119049, Russian Federation, (Russian Federation); Moscow State University, Chemistry Department, Lenins kie gory, Building 1/3, GSP-1, Moscow, 119991 (Russian Federation); Golovin, Yury I. [Moscow State University, Chemistry Department, Lenins kie gory, Building 1/3, GSP-1, Moscow, 119991 (Russian Federation); Chufarova, Nina V., E-mail: chnv@pharmcluster.ru [Moscow Institute of Physics and Technology (State University), 9 Institutskiy lane, Dolgoprudny City, Moscow Region, 141700 (Russian Federation); Beloglazkina, Elena K. [National University of Science and Technology MISiS, Leninskiy, Building 9, Moscow, 119049, Russian Federation, (Russian Federation); Moscow State University, Chemistry Department, Lenins kie gory, Building 1/3, GSP-1, Moscow, 119991 (Russian Federation); Majouga, Alexander G., E-mail: majouga@org.chem.msu.ru [National University of Science and Technology MISiS, Leninskiy, Building 9, Moscow, 119049, Russian Federation, (Russian Federation); Moscow State University, Chemistry Department, Lenins kie gory, Building 1/3, GSP-1, Moscow, 119991 (Russian Federation)

2015-11-15

Fe{sub 3}O{sub 4}@Au core/shell nanoparticles have unique magnetic and optical properties. These nanoparticles are used for biomedical applications, such as magnetic resonance imaging, photothermal therapy, controlled drug delivery, protein separation, biosensors, DNA detection, and immunosensors. In this review, recent methods for the synthesis of core/shell nanoparticles are discussed. We divided all of the synthetic methods in two groups: methods of synthesis of bi-layer structures and methods of synthesis of multilayer composite structures. The latter methods have a layer of “glue” material between the core and the shell. - Highlights: • Fe{sub 3}O{sub 4} nanoparticles are promising for biomedical applications but have some disadvantages. • Covering Fe{sub 3}O{sub 4} nanoparticles with Au shell leads to better stability and biocompatibility. • Core/shell nanoparticles are widely used for biomedical applications. • There are two types of Fe{sub 3}O{sub 4}@Au core/shell nanoparticles structures: bi-layer and multilayer composite. • Different synthetic methods enable production of nanoparticles of different sizes.

Inertial waves in a spherical shell induced by librations of the inner sphere: experimental and numerical results

Energy Technology Data Exchange (ETDEWEB)

Koch, S; Harlander, U; Egbers, C [Department of Aerodynamics and Fluid Mechanics, Brandenburg University of Technology Cottbus, Siemens-Halske-Ring 14, D-03046 Cottbus (Germany); Hollerbach, R, E-mail: uwe.harlander@tu-cottbus.de [Institute of Geophysics, ETH Zuerich, Sonneggstrasse 5, CH-8092 Zurich (Switzerland)

2013-06-15

We begin with an experimental investigation of the flow induced in a rotating spherical shell. The shell globally rotates with angular velocity {Omega}. A further periodic oscillation with angular velocity 0 Less-Than-Or-Slanted-Equal-To {omega} Less-Than-Or-Slanted-Equal-To 2{Omega}, a so-called longitudinal libration, is added on the inner sphere's rotation. The primary response is inertial waves spawned at the critical latitudes on the inner sphere, and propagating throughout the shell along inclined characteristics. For sufficiently large libration amplitudes, the higher harmonics also become important. Those harmonics whose frequencies are still less than 2{Omega} behave as inertial waves themselves, propagating along their own characteristics. The steady component of the flow consists of a prograde zonal jet on the cylinder tangent to the inner sphere and parallel to the axis of rotation, and increases with decreasing Ekman number. The jet becomes unstable for larger forcing amplitudes as can be deduced from the preliminary particle image velocimetry observations. Finally, a wave attractor is experimentally detected in the spherical shell as the pattern of largest variance. These findings are reproduced in a two-dimensional numerical investigation of the flow, and certain aspects can be studied numerically in greater detail. One aspect is the scaling of the width of the inertial shear layers and the width of the steady jet. Another is the partitioning of the kinetic energy between the forced wave, its harmonics and the mean flow. Finally, the numerical simulations allow for an investigation of instabilities, too local to be found experimentally. For strong libration amplitudes, the boundary layer on the inner sphere becomes unstable, triggering localized Goertler vortices during the prograde phase of the forcing. This instability is important for the transition to turbulence of the spherical shell flow. (paper)

Fabrication of core-shell Fe{sub 3}O{sub 4}@MIL-100(Fe) magnetic microspheres for the removal of Cr(VI) in aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Yang, Qingxiang, E-mail: qxyangzz@163.com; Zhao, Qianqian; Ren, ShuangShuang; Lu, Qiongqiong; Guo, Xinmeng; Chen, Zhijun, E-mail: chenzj@zzuli.edu.cn

2016-12-15

Facile regeneration of an adsorbent is very important for commercial feasibility. One typical highly porous metal-organic framework (MOF) materials based on MIL-100(Fe) and magnetic iron oxide particles (denoted as MMCs) with diameter about of 350 nm were successfully synthesized. The growth of MIL-100(Fe) shell on the surface of Fe{sub 3}O{sub 4} was utilized precursor as crystal seed via in-situ step hydrothermal reaction. It is a simple way to obtain well organized core-shell MOF composites, compared to the step-by-step method. MMCs were firstly used to uptake of Cr(VI) anions in aqueous solution. Adsorption experiments were carried out in batch sorption mode investigating with the factors of contact time (0–1000 min), pH (from 2 to 12), dose of adsorbent (4–25 mg), and initial Cr(VI) concentration (range from 10 to 100 ppm). - Graphical abstract: One typical highly porous metal-organic framework (MOF) materials based on MIL-100(Fe) and magnetic iron oxide particles (denoted as MMCs) were successfully synthesized. Utilizing Fe{sub 3}O{sub 4} precursor as crystal seed to grow MIL-100(Fe) shell by in-situ step hydrothermal reaction. It is a simple way to obtain core-shell MOF composites. MMCs could effectively uptake of Cr(VI) anions in aqueous solution. - Highlights: • Fe{sub 3}O{sub 4}@MIL-100(Fe) composites with core-shell structure were successfully prepared through a simple method. • The influence factors on Cr(VI) adsorption by Fe{sub 3}O{sub 4}@MIL-100(Fe) were investigated. • Cr(VI) can efficiently adsorbed by Fe{sub 3}O{sub 4}@MIL-100(Fe) composites from aqueous solution.

Facile synthesis and excellent microwave absorption properties of FeCo-C core-shell nanoparticles

Science.gov (United States)

Liang, Bingbing; Wang, Shiliang; Kuang, Daitao; Hou, Lizhen; Yu, Bowen; Lin, Liangwu; Deng, Lianwen; Huang, Han; He, Jun

2018-02-01

FeCo-C core-shell nanoparticles (NPs) with diameters of 10-50 nm have been fabricated on a large scale by one-step metal-organic chemical vapor deposition using the mixture of cobalt acetylacetonate and iron acetylacetonate as the precursor. The Fe/Co molar ratio of the alloy nanocores and graphitization degree of C shells, and thus the magnetic and electric properties of the core-shell NPs, can be tuned by the deposition temperature ranging from 700 °C to 900 °C. Comparative tests reveal that a relatively high Fe/Co molar ratio and low graphitization degree benefit the microwave absorption (MA) performance of the core-shell NPs. The composite with 20 wt% core-shell NP obtained at 800 °C and 80 wt% paraffin exhibits an optimal reflection loss ({{R}}{{L}}) of -60.4 dB at 7.5 GHz with a thickness of 3.3 mm, and an effective absorption bandwidth (frequency range for RL ≤10 dB) of 9.2 GHz (8.8-18.0 GHz) under an absorber thickness of 2.5 mm. Our study provides a facile route for the fabrication of alloy-C core-shell nanostructures with high MA performance.

Studies of fluorescence and Auger decay following inner-shell photoionization

International Nuclear Information System (INIS)

Levin, J.C.; Armen, G.B.

2004-01-01

Near inner-shell absorption edges, Auger and fluorescence spectra which characterize the first step of a complex cascade process exhibit properties which are well described by radiationless and radiative resonant Raman scattering theory. We present comparisons of our recent data and theory for Auger decay of argon K vacancies, xenon L vacancies, and of fluorescence decay of xenon L vacancies. A theoretical unification of Auger decay and fluorescence decay is presented which clarifies the similarities and differences between the two processes

Multi-photon excited luminescence of magnetic FePt core-shell nanoparticles.

Science.gov (United States)

Seemann, K M; Kuhn, B

2014-07-01

We present magnetic FePt nanoparticles with a hydrophilic, inert, and biocompatible silico-tungsten oxide shell. The particles can be functionalized, optically detected, and optically manipulated. To show the functionalization the fluorescent dye NOPS was bound to the FePt core-shell nanoparticles with propyl-triethoxy-silane linkers and fluorescence of the labeled particles were observed in ethanol (EtOH). In aqueous dispersion the NOPS fluorescence is quenched making them invisible using 1-photon excitation. However, we observe bright luminescence of labeled and even unlabeled magnetic core-shell nanoparticles with multi-photon excitation. Luminescence can be detected in the near ultraviolet and the full visible spectral range by near infrared multi-photon excitation. For optical manipulation, we were able to drag clusters of particles, and maybe also single particles, by a focused laser beam that acts as optical tweezers by inducing an electric dipole in the insulated metal nanoparticles. In a first application, we show that the luminescence of the core-shell nanoparticles is bright enough for in vivo multi-photon imaging in the mouse neocortex down to cortical layer 5.

Fabrication of Fe{sub 3}O{sub 4}@CuO core-shell from MOF based materials and its antibacterial activity

Energy Technology Data Exchange (ETDEWEB)

Rajabi, S.K. [Department of Chemistry, University of Guilan, University Campus 2, Rasht (Iran, Islamic Republic of); Sohrabnezhad, Sh., E-mail: sohrabnezhad@guilan.ac.ir [Department of Chemistry, Faculty of Science, University of Guilan, P.O. Box 1914, Rasht (Iran, Islamic Republic of); Ghafourian, S. [Clinical Microbiology Research Center, Ilam University of Medical Sciences, Ilam (Iran, Islamic Republic of)

2016-12-15

Magnetic Fe{sub 3}O{sub 4}@CuO nanocomposite with a core/shell structure was successfully synthesized via direct calcinations of magnetic Fe{sub 3}O{sub 4}@HKUST-1 in air atmosphere. The morphology, structure, magnetic and porous properties of the as-synthesized nano composites were characterized by using scanning electron microscope (SEM), transmission electron microscopy (TEM), powder X-ray diffraction (PXRD), and vibration sample magnetometer (VSM). The results showed that the nanocomposite material included a Fe{sub 3}O{sub 4} core and a CuO shell. The Fe{sub 3}O{sub 4}@CuO core-shell can be separated easily from the medium by a small magnet. The antibacterial activity of Fe{sub 3}O{sub 4}-CuO core-shell was investigated against gram-positive and gram-negative bacteria. A new mechanism was proposed for inactivation of bacteria over the prepared sample. It was demonstrated that the core-shell exhibit recyclable antibacterial activity, acting as an ideal long-acting antibacterial agent. - Graphical abstract: Fe{sub 3}O{sub 4}@CuO core-shell release of copper ions. These Cu{sup 2+} ions were responsible for the exhibited antibacterial activity. - Highlights: • The Fe{sub 3}O{sub 4}@CuO core-shell was prepared by MOF method. • This is the first study of antibacterial activity of core-shell consist of CuO and Fe{sub 3}O{sub 4}. • The core-shell can be reused effectively. • Core-shell was separated from the reaction solution by external magnetic field.

Fabrication of Fe3O4@CuO core-shell from MOF based materials and its antibacterial activity

Science.gov (United States)

Rajabi, S. K.; Sohrabnezhad, Sh.; Ghafourian, S.

2016-12-01

Magnetic Fe3O4@CuO nanocomposite with a core/shell structure was successfully synthesized via direct calcinations of magnetic Fe3O4@HKUST-1 in air atmosphere. The morphology, structure, magnetic and porous properties of the as-synthesized nano composites were characterized by using scanning electron microscope (SEM), transmission electron microscopy (TEM), powder X-ray diffraction (PXRD), and vibration sample magnetometer (VSM). The results showed that the nanocomposite material included a Fe3O4 core and a CuO shell. The Fe3O4@CuO core-shell can be separated easily from the medium by a small magnet. The antibacterial activity of Fe3O4-CuO core-shell was investigated against gram-positive and gram-negative bacteria. A new mechanism was proposed for inactivation of bacteria over the prepared sample. It was demonstrated that the core-shell exhibit recyclable antibacterial activity, acting as an ideal long-acting antibacterial agent.

A Core-Shell Fe/Fe2 O3 Nanowire as a High-Performance Anode Material for Lithium-Ion Batteries.

Science.gov (United States)

Na, Zhaolin; Huang, Gang; Liang, Fei; Yin, Dongming; Wang, Limin

2016-08-16

The preparation of novel one-dimensional core-shell Fe/Fe2 O3 nanowires as anodes for high-performance lithium-ion batteries (LIBs) is reported. The nanowires are prepared in a facile synthetic process in aqueous solution under ambient conditions with subsequent annealing treatment that could tune the capacity for lithium storage. When this hybrid is used as an anode material for LIBs, the outer Fe2 O3 shell can act as an electrochemically active material to store and release lithium ions, whereas the highly conductive and inactive Fe core functions as nothing more than an efficient electrical conducting pathway and a remarkable buffer to tolerate volume changes of the electrode materials during the insertion and extraction of lithium ions. The core-shell Fe/Fe2 O3 nanowire maintains an excellent reversible capacity of over 767 mA h g(-1) at 500 mA g(-1) after 200 cycles with a high average Coulombic efficiency of 98.6 %. Even at 2000 mA g(-1) , a stable capacity as high as 538 mA h g(-1) could be obtained. The unique composition and nanostructure of this electrode material contribute to this enhanced electrochemical performance. Due to the ease of large-scale fabrication and superior electrochemical performance, these hybrid nanowires are promising anode materials for the next generation of high-performance LIBs. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Negative impact of oxygen molecular activation on Cr(VI) removal with core–shell Fe@Fe2O3 nanowires

International Nuclear Information System (INIS)

Mu, Yi; Wu, Hao; Ai, Zhihui

2015-01-01

Highlights: • The presence of oxygen inhibited Cr(VI) removal efficiency with nZVI by near 3 times. • Cr(VI) removal with nZVI was related to adsorption, reduction, co-precipitation, and adsorption reactions. • Molecular oxygen activation competed donor electrons from Fe 0 core and surface bound Fe(II) of nZVI. • Thicker Cr(III)/Fe(III)/Cr(VI) oxyhydroxides shell of nZVI leaded to the electron transfer inhibition. - Abstract: In this study, we demonstrate that the presence of oxygen molecule can inhibit Cr(VI) removal with core–shell Fe@Fe 2 O 3 nanowires at neutral pH of 6.1. 100% of Cr(VI) removal was achieved by the Fe@Fe 2 O 3 nanowires within 60 min in the anoxic condition, in contrast, only 81.2% of Cr(VI) was sequestrated in the oxic condition. Removal kinetics analysis indicated that the presence of oxygen could inhibit the Cr(VI) removal efficiency by near 3 times. XRD, SEM, and XPS analysis revealed that either the anoxic or oxic Cr(VI) removal was involved with adsorption, reduction, co-precipitation, and re-adsorption processes. More Cr(VI) was bound in a reduced state of Cr(III) in the anoxic process, while a thicker Cr(III)/Fe(III)/Cr(VI) oxyhydroxides shell, leading to inhibiting the electron transfer, was found under the oxic process. The negative impact of oxygen molecule was attributed to the oxygen molecular activation which competed with Cr(VI) adsorbed for the consumption of donor electrons from Fe 0 core and ferrous ions bound on the iron oxides surface under the oxic condition. This study sheds light on the understanding of the fate and transport of Cr(VI) in oxic and anoxic environment, as well provides helpful guide for optimizing Cr(VI) removal conditions in real applications

Stability of inner baffle-shell of pool type LMFBR - experimental and theoretical studies

International Nuclear Information System (INIS)

Lebey, J.; Combescure, A.

1987-01-01

I pool type LMFBR, the primary coolant circuit, inside the main vessel, comprises a hot plenum separated from a cold plenum by an inner baffle. For Superphenix 1 reactor, it was judged advisable to built a double-shell baffle, each shell withstanding only one type of loading (primary loading for one shell, secondary loading for the other). Due to the size and intricacy of the structure, this design involves unnegligible supplementary costs and manufacturing difficulties. Thus, an alternative solution has been studied for future plants projects. It consists of a single shell baffle having a shape especially studied to sustain the two types of applied loadings (thermal plus primary loadings). Such a shape was calculated by NOVATOME, and it was decided to check the ability of methods of analysis to predict the ruin of this structure under primary loading. For this purpose, a mock-up has been tested, and the experimental results compared with the calculated ones. (orig./GL)

A Highly Stable and Magnetically Recyclable Nanocatalyst System: Mesoporous Silica Spheres Embedded with FeCo/Graphitic Shell Magnetic Nanoparticles and Pt Nanocatalysts.

Science.gov (United States)

Kim, Da Jeong; Li, Yan; Kim, Yun Jin; Hur, Nam Hwi; Seo, Won Seok

2015-12-01

We have developed a highly stable and magnetically recyclable nanocatalyst system for alkene hydrogenation. The materials are composed of mesoporous silica spheres (MSS) embedded with FeCo/graphitic shell (FeCo/GC) magnetic nanoparticles and Pt nanocatalysts (Pt-FeCo/GC@MSS). The Pt-FeCo/GC@MSS have superparamagnetism at room temperature and show type IV isotherm typical for mesoporous silica, thereby ensuring a large enough inner space (surface area of 235.3 m(2)  g(-1), pore volume of 0.165 cm(3)  g(-1), and pore diameter of 2.8 nm) to undergo catalytic reactions. We have shown that the Pt-FeCo/GC@MSS system readily converts cyclohexene into cyclohexane, which is the only product isolated and Pt-FeCo/GC@MSS can be seperated very quickly by an external magnetic field after the catalytic reaction is finished. We have demonstrated that the recycled Pt-FeCo/GC@MSS can be reused further for the same hydrogenation reaction at least four times without loss in the initial catalytic activity. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Ionization effects in electronic inner-shells of ionized atoms

International Nuclear Information System (INIS)

Shchornak, G.

1983-01-01

A review of the atomic physics of ionization atoms has been presented. Interaction and structure effects in atomic shells, correlated to the occurrence of vacancies in several subshells of the atom have been considered. The methods of calculations of atomic states and wave functions have been reviewed. The energy shift of characteristic X-rays is discussed as a function of the ionization stage of the atom. The influence of inner and outer-shell vacancies on the energy of the X-rays is shown in detail. The influence of chemical effects on the parameters of X-rays is also taken into account. Further on, the change of transition probabilities in radiative and non-radiative transitions by changing stage of ionization is discussed; and among them the leading part of Auger and Coster-Kronig transitions by the arearrangement of the atomic states is shown. The influence of non-radiative electronic transitions on ionization cross-sections for multiple ionization is discussed. Using these results, ionization cross-sections for direct and indirect processes for several ionization stages are given

Hot rotating fp shell Fe isotopes near proton drip line

International Nuclear Information System (INIS)

Aggarwal, Mamta

2003-01-01

F p shell 44-58 Fe nuclei have been investigated in highly excited state using the statistical theory of hot rotating nucleus. Effects of thermal and rotational excitation at drip line nuclei are studied

The SCA description of inner-shell Coulomb ionization and associated phenomena

International Nuclear Information System (INIS)

Hansteen, J.M.

1989-01-01

The semiclassical trajectory method for describing atomic processes induced by charged projectiles is outlined. The framework for the perturbative SCA formalism is sketched with emphasis on the first-order time-dependent approach. Selected results from computations on inner-shell Coulomb ionization and δ-electron emission are presented. The kinematic scaling law for ionization and pair-production phenomena is treated in detail. The importance of this scaling law for high-energy atomic collision physics is stressed. (orig.)

Recent evolution of theoretical models in inner shell photoionization

International Nuclear Information System (INIS)

Combet Farnoux, F.

1978-01-01

This paper is a brief review of various atomic theoretical models recently developed to calculate photoionization cross sections in the low energy range (from the far ultraviolet to the soft X ray region). For both inner and outer shells concerned, we emphasize the necessity to go beyond the independent particle models by means of the introduction of correlation effects in both initial and final states. The basic physical ideas of as elaborated models as Random Phase Approximation with exchange, Many Body Perturbation Theory and R matrix Theory are outlined and summarized. As examples, the results of some calculations are shown and compared with experiment

In-depth nanocrystallization enhanced Li-ions batteries performance with nitrogen-doped carbon coated Fe3O4 yolk-shell nanocapsules

Science.gov (United States)

Wu, Qianhui; Zhao, Rongfang; Liu, Wenjie; Zhang, Xiue; Shen, Xiao; Li, Wenlong; Diao, Guowang; Chen, Ming

2017-03-01

In this paper nitrogen-doped carbon-encapsulation Fe3O4 yolk-shell magnetic nanocapsules (Fe3O4@C-N nanocapsules) have been successfully constructed though a facile hydrothermal method and subsequent annealing process. Fe3O4 nanoparticles are completely enclosed in nitrogen-doped carbon shells with void space between the nanoparticle and the shell. The yolk-shell structure allows Fe3O4 nanoparticles to expand freely without breaking the outer carbon shell during the lithiation/delithiation processes. The volume expansion of Fe3O4 results in the in-depth nanocrystallization. Fortunately, the new generated small nanoparticles can increase the capability with the cycle increase due to the unique confinement effect and excellent electronic conductivity of the nitrogen-doped carbon shells. Hence, after 150 cycles, the discharge capacity of Fe3O4@C-N-700 nanocapsules still remained 832 mA h g-1 at 500 mA g-1, which corresponds to 116.7% of the lowest capacity (713 mA h g-1) at the 16th cycle. We believe that the yolk-shell structure is conducive to enhance the capacity of easy pulverization metal oxidation during the charge/discharge processes.

Cross Sections for Inner-Shell Ionization by Electron Impact

Energy Technology Data Exchange (ETDEWEB)

Llovet, Xavier, E-mail: xavier@ccit.ub.edu [Centres Científics i Tecnològics, Universitat de Barcelona, Lluís Solé i Sabarís 1-3, 08028 Barcelona (Spain); Powell, Cedric J. [Materials Measurement Science Division, National Institute of Standards and Technology, Gaithersburg, Maryland 20899-8370 (United States); Salvat, Francesc [Facultat de Física (ECM and ICC), Universitat de Barcelona, Diagonal 645, 08028 Barcelona (Spain); Jablonski, Aleksander [Institute of Physical Chemistry, Polish Academy of Sciences, ul. Kasprzaka 44/52, 01-224 Warsaw (Poland)

2014-03-15

An analysis is presented of measured and calculated cross sections for inner-shell ionization by electron impact. We describe the essentials of classical and semiclassical models and of quantum approximations for computing ionization cross sections. The emphasis is on the recent formulation of the distorted-wave Born approximation by Bote and Salvat [Phys. Rev. A 77, 042701 (2008)] that has been used to generate an extensive database of cross sections for the ionization of the K shell and the L and M subshells of all elements from hydrogen to einsteinium (Z = 1 to Z = 99) by electrons and positrons with kinetic energies up to 1 GeV. We describe a systematic method for evaluating cross sections for emission of x rays and Auger electrons based on atomic transition probabilities from the Evaluated Atomic Data Library of Perkins et al. [Lawrence Livermore National Laboratory, UCRL-ID-50400, 1991]. We made an extensive comparison of measured K-shell, L-subshell, and M-subshell ionization cross sections and of Lα x-ray production cross sections with the corresponding calculated cross sections. We identified elements for which there were at least three (for K shells) or two (for L and M subshells) mutually consistent sets of cross-section measurements and for which the cross sections varied with energy as expected by theory. The overall average root-mean-square deviation between the measured and calculated cross sections was 10.9% and the overall average deviation was −2.5%. This degree of agreement between measured and calculated ionization and x-ray production cross sections was considered to be very satisfactory given the difficulties of these measurements.

Nano-sized LiFePO4/C composite with core-shell structure as cathode material for lithium ion battery

International Nuclear Information System (INIS)

Liu, Yang; Zhang, Min; Li, Ying; Hu, Yemin; Zhu, Mingyuan; Jin, Hongming; Li, Wenxian

2015-01-01

Graphical abstract: Nano-sized LiFePO4/C composite with core-shell structure was fabricated via a well-designed approach as cathode material forlithium ion battery. The nano-sized LiFePO4/C composite with whole carbon shell coating layer showed an excellent electrical performance. - Abstract: Nano-sized composite with LiFePO 4 -core and carbon-shell was synthesized via a facile route followed by heat treatment at 650 °C. X-ray diffraction (XRD) shows that the core is well crystallized LiFePO 4 . The electron microscopy (SEM and TEM) observations show that the core-shell structured LiFePO 4 /C composite coating with whole carbon shell layer of ∼2.8 nm, possesses a specific surface area of 51 m 2 g −1 . As cathode material for lithium ion battery, the core-shell LiFePO 4 /C composite exhibits high initial capacity of 161 mAh g −1 at 0.1 C, excellent high-rate discharge capacity of 135 mAh g −1 at 5 C and perfect cycling retention of 99.6% at 100 th cycle. All these promising results should be contributed to the core-shell nanostructure which prevents collapse of the particle structure in the long-term charge and discharge cycles, as well as the large surface area of the nano-sized LiFePO 4 /C composite which enhances the electronic conductivity and shortens the distance of lithium ion diffusion

Enhanced Performance of Photoelectrochemical Water Splitting with ITO@α-Fe2O3 Core-Shell Nanowire Array as Photoanode.

Science.gov (United States)

Yang, Jie; Bao, Chunxiong; Yu, Tao; Hu, Yingfei; Luo, Wenjun; Zhu, Weidong; Fu, Gao; Li, Zhaosheng; Gao, Hao; Li, Faming; Zou, Zhigang

2015-12-09

Hematite (α-Fe2O3) is one of the most promising candidates for photoelectrodes in photoelectrochemical water splitting system. However, the low visible light absorption coefficient and short hole diffusion length of pure α-Fe2O3 limits the performance of α-Fe2O3 photoelectrodes in water splitting. Herein, to overcome these drawbacks, single-crystalline tin-doped indium oxide (ITO) nanowire core and α-Fe2O3 nanocrystal shell (ITO@α-Fe2O3) electrodes were fabricated by covering the chemical vapor deposited ITO nanowire array with compact thin α-Fe2O3 nanocrystal film using chemical bath deposition (CBD) method. The J-V curves and IPCE of ITO@α-Fe2O3 core-shell nanowire array electrode showed nearly twice as high performance as those of the α-Fe2O3 on planar Pt-coated silicon wafers (Pt/Si) and on planar ITO substrates, which was considered to be attributed to more efficient hole collection and more loading of α-Fe2O3 nanocrystals in the core-shell structure than planar structure. Electrochemical impedance spectra (EIS) characterization demonstrated a low interface resistance between α-Fe2O3 and ITO nanowire arrays, which benefits from the well contact between the core and shell. The stability test indicated that the prepared ITO@α-Fe2O3 core-shell nanowire array electrode was stable under AM1.5 illumination during the test period of 40,000 s.

Inner shell coulomb ionization by light ions: applications of the semiclassical approximation

International Nuclear Information System (INIS)

Kocbach, L.

1976-01-01

The Semiclassical Approximation (SCA) has been applied to the process of inner shell ionization by Bang and Hansteen (1959). In the process of the present work their formalism has been simplified. Numerical results have been obtained and compared with experimental data for K- and L-shell ionization. Results for M-shell ionization were also obtained. Three effects have been investigated in close collaboration with experimentalists: structure in the distribution of L-shell ionization probabilities; relativistic effects; angular dependence of ionization probability for very small impact parameters. The structure of the mechanism has been discussed, and, for the first time in the SCA framework, realistic electronic wave functions have been used in the calculations of ionization cross sections and probabilities. This work is not thereby completed and many aspects require further study. The review part of the thesis should thus also provide a reference system for further work. Three of the papers contain general discussions and to some extent have the character of review papers. Appendix A of the review paper forms a cross-reference index for the papers included, while a list of papers on SCA by the Bergen Group is given in Appendix B. (Auth.)

Oxidative degradation of the antibiotic oxytetracycline by Cu@Fe3O4 core-shell nanoparticles.

Science.gov (United States)

Pham, Van Luan; Kim, Do-Gun; Ko, Seok-Oh

2018-08-01

A core-shell nanostructure composed of zero-valent Cu (core) and Fe 3 O 4 (shell) (Cu@Fe 3 O 4 ) was prepared by a simple reduction method and was evaluated for the degradation of oxytetracycline (OTC), an antibiotic. The Cu core and the Fe 3 O 4 shell were verified by X-ray diffractometry (XRD) and transmission electron microscopy. The optimal molar ratio of [Cu]/[Fe] (1/1) in Cu@Fe 3 O 4 created an outstanding synergic effect, leading to >99% OTC degradation as well as H 2 O 2 decomposition within 10min at the reaction conditions of 1g/L Cu@Fe 3 O 4 , 20mg/L OTC, 20mM H 2 O 2 , and pH3.0 (and even at pH9.0). The OTC degradation rate by Cu@Fe 3 O 4 was higher than obtained using single nanoparticle of Cu or Fe 3 O 4 . The results of the study using radical scavengers showed that OH is the major reactive oxygen species contributing to the OTC degradation. Finally, good stability, reusability, and magnetic separation were obtained with approximately 97% OTC degradation and no notable change in XRD patterns after the Cu@Fe 3 O 4 catalyst was reused five times. These results demonstrate that Cu@Fe 3 O 4 is a novel prospective candidate for the pharmaceutical and personal care products degradation in the aqueous phase. Copyright © 2018 Elsevier B.V. All rights reserved.

Inner-shell photoemission from atoms and molecules using synchrotron radiation

International Nuclear Information System (INIS)

Lindle, D.W.

1983-12-01

Photoelectron spectroscopy, in conjunction with synchrotron radiation, has been used to study inner-shell photoemission from atoms and molecules. The time structure of the synchrotron radiation permits the measurements of time-of-flight (TOF) spectra of Auger and photoelectrons, thereby increasing the electron collection efficiency. The double-angle TOF method yielded angle-resolved photoelectron intensities, which were used to determine photoionization cross sections and photoelectron angular distributions in several cases. Comparison to theoretical calculations has been made where possible to help explain observed phenomena in terms of the electronic structure and photoionization dynamics of the systems studied. 154 references, 23 figures, 7 tables

Investigating the Role of Shell Thickness and Field Cooling on Saturation Magnetization and Its Temperature Dependence in Fe3O4/γ-Fe2O3 Core/Shell Nanoparticles

Directory of Open Access Journals (Sweden)

Ihab M. Obaidat

2017-12-01

Full Text Available Understanding saturation magnetization and its behavior with particle size and temperature are essential for medical applications such magnetic hyperthermia. We report the effect of shell thickness and field cooling on the saturation magnetization and its behavior with temperature in Fe3O4/γ-Fe2O3 core/shell nanoparticles of fixed core diameter (8 nm and several shell thicknesses. X-ray diffraction (XRD analysis and transmission electron microscopy (TEM, high-resolution transmission electron microscopy (HRTEM were used to investigate the phase and the morphology of the samples. Selected area electron diffraction (SAED confirmed the core/shell structure and phases. Using a SQUID (San Diego, CA, USA, magnetic measurements were conducted in the temperature range of 2 to 300 K both under zero field-cooling (ZFC and field-cooling (FC protocols at several field-cooling values. In the ZFC state, considerable enhancement of saturation magnetization was obtained with the increase of shell thickness. After field cooling, we observed a drastic enhancement of the saturation magnetization in one sample up to 120 emu/g (50% larger than the bulk value. In both the FC and ZFC states, considerable deviations from the original Bloch’s law were observed. These results are discussed and attributed to the existence of interface spin-glass clusters which are modified by the changes in the shell thickness and the field-cooling.

Magnetic Behavior of Ni-Fe Core-Shell and Alloy Nanowires

Science.gov (United States)

Tripathy, Jagnyaseni; Vargas, Jose; Spinu, Leonard; Wiley, John

2013-03-01

Template assisted synthesis was used to fabricate a series of Ni-Fe core-shell and alloy nanowires. By controlling reaction conditions as well as pore structure, both systems could be targeted and magnetic properties followed as a function of architectures. In the core-shell structure coercivity increases with decrease in shell thickness while for the alloys, coercivity squareness improve with increase pore diameter. Details on the systematic studies of these materials will be presented in terms of hysteretic measurements, including first order reversal curves (FORC), and FMR data. Magnetic variation as a function of structure and nanowire aspect ratios will be presented and the origins of these behaviors discussed. Advanced Material Research Institute

Synthesis and characterization of core-shell Fe3O4-gold-chitosan nanostructure

Directory of Open Access Journals (Sweden)

Salehizadeh Hossein

2012-01-01

Full Text Available Abstract Background Fe3O4-gold-chitosan core-shell nanostructure can be used in biotechnological and biomedical applications such as magnetic bioseparation, water and wastewater treatment, biodetection and bioimaging, drug delivery, and cancer treatment. Results Magnetite nanoparticles with an average size of 9.8 nm in diameter were synthesized using the chemical co-precipitation method. A gold-coated Fe3O4 monotonous core-shell nanostructure was produced with an average size of 15 nm in diameter by glucose reduction of Au3+ which is then stabilized with a chitosan cross linked by formaldehyde. The results of analyses with X-ray diffraction (XRD, Fourier Transformed Infrared Spectroscopy (FTIR, Transmission Electron Microscopy (TEM, and Atomic Force Microscopy (AFM indicated that the nanoparticles were regularly shaped, and agglomerate-free, with a narrow size distribution. Conclusions A rapid, mild method for synthesizing Fe3O4-gold nanoparticles using chitosan was investigated. A magnetic core-shell-chitosan nanocomposite, including both the supermagnetic properties of iron oxide and the optical characteristics of colloidal gold nanoparticles, was synthesized.

Observation of Rydberg transitions from the inner valence shell of ethane

International Nuclear Information System (INIS)

Dillon, M.A.; Tanaka, H.; Spence, D.

1987-01-01

The electron impact spectrum of ethane has been examined in a region that includes ionization out of the inner valence shell. One diffuse structure and a progression of ten vibrational bands have been found in a 4 eV range below and to some degree overlapping the 2 A 2 /sub u/ ion threshold. Evidence indicates that the observed transitions belong to the symmetry forbidden Rydberg series (2a 2 /sub u/) 2 →(2a 2 /sub u/, npσ or npπ)

Magnetic Fe{sub 3}O{sub 4}-Au core-shell nanostructures for surface enhanced Raman scattering

Energy Technology Data Exchange (ETDEWEB)

Wheeler, D.A.; Adams, S.A.; Zhang, J.Z. [Department of Chemistry and Biochemistry, University of California, Santa Cruz, Santa Cruz, CA 95064 (United States); Lopez-Luke, T. [Department of Chemistry and Biochemistry, University of California, Santa Cruz, Santa Cruz, CA 95064 (United States); Cento de Investigaciones en Optica, A.P. 1-948 Leon, Gto. 37150 (Mexico); Torres-Castro, A. [Universidad Autonoma de Nuevo Leon, A.P. 126-F, Monterrey, NL, 66450 (Mexico)

2012-11-15

The synthesis, structural and optical characterization, and application of superparamagnetic and water-dispersed Fe{sub 3}O{sub 4}-Au core-shell nanoparticles for surface enhanced Raman scattering (SERS) is reported. The structure of the nanoparticles was determined by scanning transmission electron microscopy (STEM) and high-resolution transmission electron microscopy (HRTEM). STEM images of the Fe{sub 3}O{sub 4}-Au core-shell nanoparticles reveal an average diameter of 120 nm and a high degree of surface roughness. The nanoparticles, which display superparamagnetic properties due to the core Fe{sub 3}O{sub 4} material, exhibit a visible surface plasmon resonance (SPR) peaked at 580 nm due to the outer gold shell. The nanoparticles are used as a substrate for surface enhanced Raman scattering (SERS) with rhodamine 6G (R6G) as a Raman reporter molecule. The SERS enhancement factor is estimated to be on the order of 10{sup 6}, which is {proportional_to} 2 times larger than that of conventional gold nanoparticles (AuNPs) under similar conditions. Significantly, magnetically-induced aggregation of the Fe{sub 3}O{sub 4}-Au core-shell nanoparticles substantially enhanced SERS activity compared to non-magnetically-aggregated Fe{sub 3}O{sub 4}-Au nanoparticles. This is attributed to both increased scattering from the aggregates as well as ''hot spots'' due to more junction sites in the magnetically-induced aggregates. The magnetic properties of the Fe{sub 3}O{sub 4} core, coupled with the optical properties of the Au shell, make the Fe{sub 3}O{sub 4}-Au nanoparticles unique for various potential applications including biological sensing and therapy. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Contribution of inner shell Compton ionization to the X-ray fluorescence line intensity

Science.gov (United States)

Fernández, Jorge E.; Scot, Viviana; Di Giulio, Eugenio

2016-10-01

The Compton effect is a potential ionization mechanism of atoms. It produces vacancies in inner shells that are filled with the same mechanism of atomic relaxation as the one following photo-absorption. This contribution to X-ray fluorescence emission is frequently neglected because the total Compton cross-section is apparently much lower than the photoelectric one at useful X-ray energies. However, a more careful analysis suggests that is necessary to consider single shell cross sections (instead of total cross sections) as a function of energy. In this article these Compton cross sections are computed for the shells K, L1-L3 and M1-M5 in the framework of the impulse approximation. By comparing the Compton and the photoelectric cross-section for each shell it is then possible to determine the extent of the Compton correction to the intensity of the corresponding characteristic lines. It is shown that for the K shell the correction becomes relevant for excitation energies which are too high to be influent in X-ray spectrometry. In contrast, for L and M shells the Compton contribution is relevant for medium-Z elements and medium energies. To illustrate the different grades of relevance of the correction, for each ionized shell, the energies for which the Compton contribution reaches the extent levels of 1, 5, 10, 20, 50 and 100% of the photoelectric one are determined for all the elements with Z = 11-92. For practical applications it is provided a simple formula and fitting coefficients to compute average correction levels for the shells considered.

Synthesis of Fe5C2@SiO2 core@shell nanoparticles as a potential candidate for biomedical application

Science.gov (United States)

Ahmadpoor, Fatemeh; Shojaosadati, Seyed Abbas; Delavari H, Hamid; Christiansen, Gunna; Saber, Reza

2018-05-01

A new strategy for water-dispersibility of hydrophobic carbide nanostructures was proposed. In this regard, hydrophobic Fe5C2 nanoparticles (NPs) with size ranging 25–40 nm were synthesized and coated with 12–15 nm silica shell for biomedical applications. X-ray diffraction (XRD) results revealed that Fe5C2 NPs with monoclinic structure were successfully prepared. The crystalline structure of Fe5C2 NPs was remained unchanged and saturation magnetization of core remained nearly constant after coating with silica shell. Moreover, Raman spectroscopy identified D-band of amorphous carbon shells which was also confirmed by transmission electron microscopy (TEM). Finally, Fe5C2@SiO2 core@shell NPs demonstrated no significant cytotoxicity and appropriate heat generating which makes them a promising candidate for magnetic fluid hyperthermia applications.

The influence of oxidation process on exchange bias in egg-shaped FeO/Fe{sub 3}O{sub 4} core/shell nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Leszczyński, Błażej, E-mail: b.leszczynski@amu.edu.pl [NanoBioMedical Centre, Adam Mickiewicz University, Umultowska 85, 61-614 Poznań (Poland); Faculty of Physics, Adam Mickiewicz University, Umultowska 85, 61-614 Poznań (Poland); Hadjipanayis, George C.; El-Gendy, Ahmed A. [Department of Physics and Astronomy, University of Delaware, 217 Sharp Lab, Newark, DE 19716 (United States); Załęski, Karol [NanoBioMedical Centre, Adam Mickiewicz University, Umultowska 85, 61-614 Poznań (Poland); Śniadecki, Zbigniew [Institute of Molecular Physics, Polish Academy of Sciences, M. Smoluchowskiego 17, 60-179 Poznań (Poland); Musiał, Andrzej [NanoBioMedical Centre, Adam Mickiewicz University, Umultowska 85, 61-614 Poznań (Poland); Institute of Molecular Physics, Polish Academy of Sciences, M. Smoluchowskiego 17, 60-179 Poznań (Poland); Jarek, Marcin [NanoBioMedical Centre, Adam Mickiewicz University, Umultowska 85, 61-614 Poznań (Poland); Jurga, Stefan [NanoBioMedical Centre, Adam Mickiewicz University, Umultowska 85, 61-614 Poznań (Poland); Faculty of Physics, Adam Mickiewicz University, Umultowska 85, 61-614 Poznań (Poland); Skumiel, Andrzej [Faculty of Physics, Adam Mickiewicz University, Umultowska 85, 61-614 Poznań (Poland)

2016-10-15

Egg-shaped nanoparticles with a core–shell morphology were synthesized by thermal decomposition of an iron oleate complex. XRD and M(T) magnetic measurements confirmed the presence of FeO (wustite) and Fe{sub 3}O{sub 4} (magnetite) phases in the nanoparticles. Oxidation of FeO to Fe{sub 3}O{sub 4} was found to be the mechanism for the shell formation. As-made nanoparticles exhibited high values of exchange bias at 2 K. Oxidation led to decrease of exchange field from 2880 Oe (in as-made sample) to 330 Oe (in oxidized sample). At temperatures higher than the Néel temperature of FeO (200 K) there was no exchange bias. An interesting observation was made showing the exchange field to be higher than the coercive field at temperatures close to magnetite's Verwey transition. - Highlights: • Synthesis of monodispersed FeO nanoparticles is shown. • As-made FeO nanoparticle is antiferromagnetically ordered, when it is oxidized to Fe{sub 3}O{sub 4}, the FeO core becomes small and disordered. • Exchange bias in well-ordered and disordered core is different.

Thick-target method in the measurement of inner-shell ionization cross-sections by low-energy electron impact

International Nuclear Information System (INIS)

An, Z.; Wu, Y.; Liu, M.T.; Duan, Y.M.; Tang, C.H.

2006-01-01

In this paper, we have studied the thick-target method for the measurements of atomic inner-shell ionization cross-section or X-ray production cross-section by keV electron impact. We find that in the processes of electron impact on the thick targets, the ratios of the characteristic X-ray yields of photoelectric ionization by bremsstrahlung to the total characteristic X-ray yields are Z-dependent and shell-dependent, and the ratios also show the weak energy-dependence. In addition, in the lower incident energy region (i.e. U < 5-6), the contribution from the rediffusion effect and the secondary electrons can be negligible. In general, the thick-target method can be appropriately applied to the measurements of atomic inner-shell ionization cross-sections or X-ray production cross-sections by electron impact for low and medium Z elements in the lower incident electron energy (i.e. U < 5-6). The experimental accuracies by the thick-target method can reach to the level equivalent or superior to the accuracies of experimental data based on the thin-target method. This thick-target method has been applied to the measurement of K-shell ionization cross-sections of Ni element by electron impact in this paper

Core/shell Fe{sub 3}O{sub 4}/BiOI nanoparticles with high photocatalytic activity and stability

Energy Technology Data Exchange (ETDEWEB)

Zheng, Liyun, E-mail: zhengliyun@126.com [Hebei University of Engineering, College of Materials Science and Engineering (China); Wang, Shuling; Zhao, Lixin [Hebei University of Engineering, College of Mechanical and Equipment Engineering (China); Zhao, Shuguo [Handan Polytechnic College, Mechanical and Electrical Department (China)

2016-11-15

Core/shell Fe{sub 3}O{sub 4}/BiOI nanoparticles with BiOI sheath have been synthesized by a solvothermal reaction method and were characterized by transmission electron microscopy (TEM) with an energy dispersive spectrum (EDS), high-resolution TEM and X-ray diffraction (XRD). Their photocatalytic activities were evaluated by methylene blue (MB) under the simulated solar light. The results indicate that the spherical Fe{sub 3}O{sub 4} particles were coated with BiOI sheath when the sample were synthesized at 160 °C with ethylene glycol and deionized water, forming a core/shell structure. The degradation rate of MB assisted with the core/shell Fe{sub 3}O{sub 4}/BiOI catalysts reached 98 % after 40-min irradiation. The catalytic performance enhancement of the core/shell Fe{sub 3}O{sub 4}/BiOI catalysts mainly attributes to the band structure that can improve the generation efficiency, separation and transfer process of the photo-induced electron–hole pairs and decrease their recombination. The magnetic Fe{sub 3}O{sub 4} core not only contributes to the efficient separation of electron and holes, but also helps catalysts be collected conveniently using a magnet for reuse. After five repeated trials, the degradation rate of MB still maintains over 90 % and the saturated magnetization of the catalysts remains 51.5 emu/g, which indicate that the core/shell Fe{sub 3}O{sub 4}/BiOI nanoparticles have excellent photocatalytic stability and are recyclable for decomposing organic pollutants under visible light irradiation.

Statistical approach of inner-shell ionization in 0.1-1.625 MeV/u Cu + Bi collisions

International Nuclear Information System (INIS)

Piticu, I.; Ciortea, C.; Enulescu, A.; Fluerasu, D.; Szilagyi, S.Z.; Micu, M.; Dumitriu, D.

1999-01-01

Experimental data of inner-shell ionization cross sections and outer-shell ionization probabilities per electron, obtained for the collision system. Cu + Bi in the energy range of 0.1-1.625 MeV/u, are in good agreement with the predictions of the statistical model of Mittleman and Wilets. The found dependence of the diffusion constant determined for different final vacancy states on the excitation (ionization) energy is in fair agreement with the model prediction. (orig.)

Statistical approach of inner-shell ionization in 0.1-1.625 MeV/u Cu + Bi collisions

Energy Technology Data Exchange (ETDEWEB)

Piticu, I.; Ciortea, C.; Enulescu, A.; Fluerasu, D.; Szilagyi, S.Z.; Micu, M.; Dumitriu, D. [Horia Hulubei National Inst. of Physics and Nuclear Engineering, Bucharest (Romania). Dept. of Experimental Physics

1999-07-01

Experimental data of inner-shell ionization cross sections and outer-shell ionization probabilities per electron, obtained for the collision system. Cu + Bi in the energy range of 0.1-1.625 MeV/u, are in good agreement with the predictions of the statistical model of Mittleman and Wilets. The found dependence of the diffusion constant determined for different final vacancy states on the excitation (ionization) energy is in fair agreement with the model prediction. (orig.)

Synthesis and characterization of Fe3O4–TiO2 core-shell nanoparticles

International Nuclear Information System (INIS)

Stefan, M.; Pana, O.; Leostean, C.; Silipas, D.; Bele, C.; Senila, M.; Gautron, E.

2014-01-01

Composite core-shell nanoparticles may have morpho-structural, magnetic, and optical (photoluminescence (PL)) properties different from each of the components considered separately. The properties of Fe 3 O 4 –TiO 2 nanoparticles can be controlled by adjusting the titania amount (shell thinness). Core–shell nanoparticles were prepared by seed mediated growth of semiconductor (TiO 2 ) through a modified sol-gel process onto preformed magnetite (Fe 3 O 4 ) cores resulted from the co-precipitation method. The structure and morphology of samples were characterized by X-ray diffraction, transmission electron microscopy (TEM), and high resolution-TEM respectively. X-ray photoelectron spectroscopy was correlated with ICP-AES. Magnetic measurements, optical absorption spectra, as well as PL spectroscopy indicate the presence of a charge/spin transfer from the conduction band of magnetite into the band gap of titania nanocrystals. The process modifies both Fe 3 O 4 and TiO 2 magnetic and optical properties, respectively.

Progress on precision measurements of inner shell transitions in highly charged ions at an ECR ion source

Energy Technology Data Exchange (ETDEWEB)

Szabo, Csilla I.; Indelicato, Paul; LeBigot, Eric-Olivier; Vallette, Alexandre; Amaro, Pedro; Guerra, Mauro; Gumberidze, Alex [Laboratoire Kastler Brossel, Ecole Normale Superieure, CNRS, Universite Pierre et Marie Curie- Paris 6, Case 74, 4 place Jussieu, F-75005 Paris (France); Centro de Fisica Atomica, CFA, Departamento de Fisica (Portugal); Faculdade de Ciencias e Tecnologia, FCT, Universidade Nova de Lisboa, 2829-516 Caparica (Portugal); Laboratoire Kastler Brossel, Ecole Normale Superieure, CNRS, Universite Pierre et Marie Curie- Paris 6, Case 74, 4 place Jussieu, F-75005 Paris (France)

2012-05-25

Inner shell transitions of highly charged ions produced in the plasma of an Electron Cyclotron Resonance Ion Source (ECRIS) were observed the first time by a Double Crystal Spectrometer (DCS). The DCS is a well-used tool in precision x-ray spectroscopy due to its ability of precision wavelength measurement traced back to a relative angle measurement. Because of its requirement for a bright x-ray source the DCS has not been used before in direct measurements of highly charged ions (HCI). Our new precision measurement of inner shell transitions in HCI is not just going to provide new x-ray standards for quantum metrology but can also give information about the plasma in which the ions reside. Ionic temperatures and with that the electron density can be determined by thorough examination of line widths measured with great accuracy.

Revealing inner shell dynamics with inelastic X-ray scattering

International Nuclear Information System (INIS)

Franck, C.

1990-01-01

One of the many opportunities provided by the Advanced Photon Source (APS) is to extend the study of intra-atomic dynamics. As a means of testing dynamic response, inelastic x-ray scattering is particularly promising since it allows us to independently vary the period of the exciting field in both space and time. As an example of this type of work, the author presents experiments performed at the Cornell High Energy Synchrotron Source (CHESS) laboratory, a prototype for the APS. This was inner shell inelastic scattering with a twist: in order to explore a new distance scale an x-ray fluorescence trigger was employed. Aside for the atomic insight gained, the experiment taught them the importance of the time structure of the synchrotron beam for coincidence experiments which are dominated by accidental events

Impact parameter sensitive study of inner-shell atomic processes in the experimental storage ring

Science.gov (United States)

Gumberidze, A.; Kozhuharov, C.; Zhang, R. T.; Trotsenko, S.; Kozhedub, Y. S.; DuBois, R. D.; Beyer, H. F.; Blumenhagen, K.-H.; Brandau, C.; Bräuning-Demian, A.; Chen, W.; Forstner, O.; Gao, B.; Gassner, T.; Grisenti, R. E.; Hagmann, S.; Hillenbrand, P.-M.; Indelicato, P.; Kumar, A.; Lestinsky, M.; Litvinov, Yu. A.; Petridis, N.; Schury, D.; Spillmann, U.; Trageser, C.; Trassinelli, M.; Tu, X.; Stöhlker, Th.

2017-10-01

In this work, we present a pilot experiment in the experimental storage ring (ESR) at GSI devoted to impact parameter sensitive studies of inner shell atomic processes for low-energy (heavy-) ion-atom collisions. The experiment was performed with bare and He-like xenon ions (Xe54+, Xe52+) colliding with neutral xenon gas atoms, resulting in a symmetric collision system. This choice of the projectile charge states was made in order to compare the effect of a filled K-shell with the empty one. The projectile and target X-rays have been measured at different observation angles for all impact parameters as well as for the impact parameter range of ∼35-70 fm.

An extension of the fenske-hall LCAO method for approximate calculations of inner-shell binding energies of molecules

Science.gov (United States)

Zwanziger, Ch.; Reinhold, J.

1980-02-01

The approximate LCAO MO method of Fenske and Hall has been extended to an all-election method allowing the calculation of inner-shell binding energies of molecules and their chemical shifts. Preliminary results are given.

The Fabrication and High-Efficiency Electromagnetic Wave Absorption Performance of CoFe/C Core-Shell Structured Nanocomposites

Science.gov (United States)

Wan, Gengping; Luo, Yongming; Wu, Lihong; Wang, Guizhen

2018-03-01

CoFe/C core-shell structured nanocomposites (CoFe@C) have been fabricated through the thermal decomposition of acetylene with CoFe2O4 as precursor. The as-prepared CoFe@C was characterized by X-ray powder diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy, transmission electron microscopy, and thermogravimetric analysis. The results demonstrate that the carbon shell in CoFe@C has a poor crystallization with a thickness about 5-30 nm and a content approximately 48.5 wt.%. Due to a good combination between intrinsic magnetic properties and high-electrical conductivity, the CoFe@C exhibits not only excellent absorption intensity but also wide frequency bandwidth. The minimum RL value of CoFe@C can reach - 44 dB at a thickness of 4.0 mm, and RL values below - 10 dB is up to 4.3 GHz at a thickness of 2.5 mm. The present CoFe@C may be a potential candidate for microwave absorption application.

Inner-shell photo-ionized X-ray laser schemes for low-Z elements

International Nuclear Information System (INIS)

Moon, S.J.; Strobel, G.L.

1994-01-01

Gain calculations for inner-shell photo-ionized lasing in C at 45 angstrom are performed. An incident x-ray source represented by a 150 eV blackbody with a rise time of 50 fsec gives a gain of order 10 cm -1 . The x-ray source and thus the driving optical laser requirements are significantly reduced as compared to what is needed for Ne at 15 angstrom. The authors expect that existing ultra-short pulse lasers can produce the required x-ray source and thus produce a table-top x-ray laser at 45 angstrom

Conference proceedings on X84 International Conference on X-ray and Inner-Shell Processes in Atoms, Molecules and Solids

International Nuclear Information System (INIS)

Meisel, A.; Finster, J.

1984-01-01

The proceedings contain 46 lectures and contributions presented at the 1984 conference. Topics of the conference were ion-atom collisions, inner-shell ionization phenomena, X-ray spectroscopy and electron spectroscopy

LARGE-AREA [Fe II] LINE MAPPING OF THE SUPERNOVA REMNANT IC 443 WITH THE IRSF/SIRIUS

Energy Technology Data Exchange (ETDEWEB)

Kokusho, Takuma; Nagayama, Takahiro; Kaneda, Hidehiro; Ishihara, Daisuke [Graduate School of Science, Nagoya University, Chikusa-ku, Nagoya 464-8602 (Japan); Lee, Ho-Gyu; Onaka, Takashi, E-mail: kokusho@u.phys.nagoya-u.ac.jp [Department of Astronomy, Graduate School of Science, University of Tokyo, Bunkyo-ku, Tokyo 113-0033 (Japan)

2013-05-01

We present the results of near-infrared (near-IR) [Fe II] line mapping of the supernova remnant IC 443 with IRSF/SIRIUS, using the two narrow-band filters tuned for the [Fe II] 1.257 {mu}m and [Fe II] 1.644 {mu}m lines. Covering a large area of 30' Multiplication-Sign 35', our observations reveal that [Fe II] filamentary structures exist all over the remnant, not only in an ionic shock shell, but also in a molecular shock shell and a central region inside the shells. With the two [Fe II] lines, we performed corrections for dust extinction to derive the intrinsic line intensities. We also obtained the intensities of thermal emission from the warm dust associated with IC 443, using the far- and mid-IR images taken with AKARI and Spitzer, respectively. As a result, we find that the [Fe II] line emission relative to the dust emission notably enhances in the inner central region. We discuss causes of the enhanced [Fe II] line emission, estimating the Fe{sup +} and dust masses.

One-pot synthesis of porous Fe{sub 3}O{sub 4} shell/silver core nanocomposites used as recyclable magnetic antibacterial agents

Energy Technology Data Exchange (ETDEWEB)

Fang, Weijun, E-mail: wjfang81@gmail.com [College of Basic Medicine, Anhui Medical University, Hefei 230032, Anhui (China); Zheng, Jun; Chen, Cheng [Center of Modern Experimental Technology, Anhui University, Hefei 230039, Anhui (China); Zhang, Huabing; Lu, Yunxia [College of Basic Medicine, Anhui Medical University, Hefei 230032, Anhui (China); Ma, Ling [Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, Fujian (China); Chen, Guangjun [College of Basic Medicine, Anhui Medical University, Hefei 230032, Anhui (China)

2014-05-01

Porous Fe{sub 3}O{sub 4} shell/silver core nanocomposites featuring sustainable and recyclable antibacterial activity have been successfully prepared via a facile one-pot hydrothermal method. The unique structural feature of the Ag@Fe{sub 3}O{sub 4} nanocomposites with Ag embedded in porous Fe{sub 3}O{sub 4} shell endows them with the ability of sustained-release of silver ions. Their antimicrobial activity studies were investigated on both Gram negative Escherichia coli and Gram positive Bacillus subtilis, which demonstrate that the nanocomposites are highly toxic to microorganisms and exhibit sustainable antibacterial activity. Besides, the Ag@Fe{sub 3}O{sub 4} nanocomposites can be separated easily from the medium by a small magnet, which provided an effective way to eliminate the residual nanosilver from the surroundings. We finally demonstrate that the recovered nanocomposites exhibit recyclable antibacterial activity, acting as an ideal long-acting antibacterial agent. - Highlights: • The porous Fe{sub 3}O{sub 4} shell/silver core nanocomposites have been successfully prepared via a simple one-pot hydrothermal method. • The as-prepared Ag@Fe{sub 3}O{sub 4} nanocomposites exhibit high antibacterial activity against both Gram-positive and Gram-negative bacteria. • The porous Fe{sub 3}O{sub 4} shell/silver core nanocomposites show a stronger antibacterial ability than the solid Fe{sub 3}O{sub 4} shell/silver core nanocomposites. • The recovery nanocomposites still have antibacterial activity and can be reused.

Flexible 3D Fe@VO2 core-shell mesh: A highly efficient and easy-recycling catalyst for the removal of organic dyes.

Science.gov (United States)

Li, Jing; Wang, Ruoqi; Su, Zhen; Zhang, Dandan; Li, Heping; Yan, Youwei

2018-10-01

Nowadays, it is extremely urgent to search for efficient and effective catalysts for water purification due to the severe worldwide water-contamination crises. Here, 3D Fe@VO 2 core-shell mesh, a highly efficient catalyst toward removal of organic dyes with excellent recycling ability in the dark is designed and developed for the first time. This novel core-shell structure is actually 304 stainless steel mesh coated by VO 2 , fabricated by an electrophoretic deposition method. In such a core-shell structure, Fe as the core allows much easier separation from the water, endowing the catalyst with a flexible property for easy recycling, while VO 2 as the shell is highly efficient in degradation of organic dyes with the addition of H 2 O 2 . More intriguingly, the 3D Fe@VO 2 core-shell mesh exhibits favorable performance across a wide pH range. The 3D Fe@VO 2 core-shell mesh can decompose organic dyes both in a light-free condition and under visible irradiation. The possible catalytic oxidation mechanism of Fe@VO 2 /H 2 O 2 system is also proposed in this work. Considering its facile fabrication, remarkable catalytic efficiency across a wide pH range, and easy recycling characteristic, the 3D Fe@VO 2 core-shell mesh is a newly developed high-performance catalyst for addressing the universal water crises. Copyright © 2018 Elsevier B.V. All rights reserved.

Yolk-Shelled C@Fe3 O4 Nanoboxes as Efficient Sulfur Hosts for High-Performance Lithium-Sulfur Batteries.

Science.gov (United States)

He, Jiarui; Luo, Liu; Chen, Yuanfu; Manthiram, Arumugam

2017-09-01

Owing to the high theoretical specific capacity (1675 mA h g -1 ) and low cost, lithium-sulfur (Li-S) batteries offer advantages for next-generation energy storage. However, the polysulfide dissolution and low electronic conductivity of sulfur cathodes limit the practical application of Li-S batteries. To address such issues, well-designed yolk-shelled carbon@Fe 3 O 4 (YSC@Fe 3 O 4 ) nanoboxes as highly efficient sulfur hosts for Li-S batteries are reported here. With both physical entrapment by carbon shells and strong chemical interaction with Fe 3 O 4 cores, this unique architecture immobilizes the active material and inhibits diffusion of the polysulfide intermediates. Moreover, due to their high conductivity, the carbon shells and the polar Fe 3 O 4 cores facilitate fast electron/ion transport and promote continuous reactivation of the active material during the charge/discharge process, resulting in improved electrochemical utilization and reversibility. With these merits, the S/YSC@Fe 3 O 4 cathodes support high sulfur content (80 wt%) and loading (5.5 mg cm -2 ) and deliver high specific capacity, excellent rate capacity, and long cycling stability. This work provides a new perspective to design a carbon/metal-oxide-based yolk-shelled framework as a high sulfur-loading host for advanced Li-S batteries with superior electrochemical properties. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

On the difference in oscillator strengths of inner shell excitations in noble gases and their alkali neighbors

International Nuclear Information System (INIS)

Amusia, M.Y.; Baltenkov, A.S.; Zhuravleva, G.I.

1995-01-01

It is demonstrated that the oscillator strength of resonant inner-shell excitation in a noble gas atom is considerably smaller than that in its alkali neighbor because in the latter case the effective charge acting upon excited electron is much bigger. With increase of the excitation's principal quantum number the difference between line intensities in noble gases and their alkali neighbors rapidly disappears. The calculations are performed in the Hartree-Fock approximation and with inclusion of rearrangement effects due to inner vacancy creation and its Auger decay. A paper has been submitted for publication

Double-shell Fe2O3 hollow box-like structure for enhanced photo-Fenton degradation of malachite green dye

Science.gov (United States)

Jiang, De Bin; Liu, Xiaoying; Xu, Xuan; Zhang, Yu Xin

2018-01-01

In this work we demonstrate the synthesis of novel Fe2O3 nanosheets with double-shell hollow morphology by replica molding from diatomite framework. The nanostructures of Fe2O3 nanosheets were examined by focused-ion-beam scanning electron microscopy (FIB/SEM), X-ray diffraction spectroscopy (XRD), Brunauer-Emmett-Teller (BET) specific surface area measurements and Fourier transform infrared (FT-IR) spectroscopy. The results reveal that (1) Pure Fe2O3 nanosheets were successfully obtained; (2) The double-shell Fe2O3 hollow structure achieved via the NaOH etching silica method was observed; (3) Fe2O3 nanosheets possessed uniformly distributed porous nanosheets. Such structural features enlarged the specific surface area of Fe2O3 nanosheets and led to more catalytic active sites. In the heterogeneous photo-Fenton reaction, the double-shell Fe2O3 hollow morphology exhibited excellent catalytic capability for the degradation of malachite green (MG) at circumneutral pH condition. Under optimum condition, MG solution was almost completely decolorized in 60 min (99.9%). The Fe2O3 nanosheets also showed good stability and recyclability, demonstrating great potential as a promising photo-Fenton catalyst for the effective degradation of MG dye in wastewater.

Computation of Ion Charge State Distributions After Inner-shell Ionization in Ne, Ar and Kr Atoms Using Monte Carlo Simulation

International Nuclear Information System (INIS)

Ahmed Ghoneim, Adel Aly; Ghoneim, Adel A.; Al-Zanki, Jasem M.; El-Essawy, Ashraf H.

2009-01-01

Atomic reorganization starts by filling the initially inner-shell vacancy by a radiative transition (x-ray) or by a non-radiative transition (Auger and Coster-Kronig processes). New vacancies created during this atomic reorganization may in turn be filled by further radiative and non-radiative transitions until all vacancies reach the outermost occupied shells. The production of inner-shell vacancy in an atom and the de-excitation decays through radiative and non-radiative transitions may result in a change of the atomic potential; this change leads to the emission of an additional electron in the continuum (electron shake-off processes). In the present work, the ion charge state distributions (CSD) and mean atomic charge ions produced from inner shell vacancy de-excitation decay are calculated for neutral Ne , Ar and Kr atoms. The calculations are carried out using Monte Carlo (MC) technique to simulate the cascade development after primary vacancy production. The radiative and non-radiative transitions for each vacancy are calculated in the simulation. In addition, the change of transition energies and transition rates due to multi vacancies produced in the atomic configurations through the cascade development are considered in the present work. It is found that considering the electron shake off process and closing of non-allowed non-radiative channels improves the results of both charge state distributions (CSD) and average charge state. To check the validity of the present calculations, the results obtained are compared with available theoretical and experimental data. The present results are found to agree well with the available theoretical and experimental values. (author)

Ultra fast atomic process in X-ray emission by inner-shell ionization

Energy Technology Data Exchange (ETDEWEB)

Moribayashi, Kengo; Sasaki, Akira [Japan Atomic Energy Research Inst., Neyagawa, Osaka (Japan). Kansai Research Establishment; Tajima, T

1998-03-01

An ultra-fast atomic process together with X-ray emission by inner-shell ionization using high intensity (10{sup 18} W/cm{sup 2}) short pulse (20fs) X-ray is studied. A new class of experiment is proposed and a useful pumping source is suggested. In this method, it is found that the gain value of X-ray laser amounts to larger than 1000(1/cm) with use of the density of 10{sup 22}/cm{sup 3} of carbon atom. Electron impact ionization effect and initial density effect as well as intensity of pumping source effect are also discussed. (author)

Inner-shell vacancy production and mean charge states of MeV/u Fe, Co, Ni and Cu ions in Au and Bi solid targets

Energy Technology Data Exchange (ETDEWEB)

Ciortea, C. E-mail: ciortea@tandem.nipne.ro; Dumitriu, Dana; Enescu, Sanda E.; Enulescu, A.; Fluerasu, Daniela; Piticu, I.; Szilagyi, Z.S

2002-06-01

The average charge states of 0.1-1.5 MeV/u Fe, Co, Ni and Cu ions in solid Au and Bi targets have been determined, by estimating the mean numbers of outer-shell spectator vacancies during the K-vacancy decay. The latter quantities were obtained from the yield and energy shifts of the K{alpha}, {beta} X-rays, by comparing with calculations in the independent electron approximation. The reported equilibrium charges, mostly characteristic for the inside of the target, are in fairly agreement with Nikolaev and Dmitriev semi-empirical formula [Phys. Lett. 28A (1968) 277].

Fe L-shell Excitation Cross Section Measurements on EBIT-I

Science.gov (United States)

Chen, Hui; Beiersdorfer, P.; Brown, G.; Boyce, K.; Kelley, R.; Kilbourne, C.; Porter, F.; Gu, M. F.; Kahn, S.

2006-09-01

We report the measurement of electron impact excitation cross sections for the strong iron L-shell 3-2 lines of Fe XVII to Fe XXIV at the LLNL EBIT-I electron beam ion trap using a crystal spectrometer and NASA-Goddard Space Flight Center's 6x6 pixel array microcalorimeter. The cross sections were determined by direct normalization to the well-established cross sections for radiative electron capture. Our results include the excitation cross section for over 50 lines at multiple electron energies. Although we have found that for 3C line in Fe XVII the measured cross sections differ significantly from theory, in most cases the measurements and theory agree within 20%. This work was performed under the auspices of the U.S. DOE by LLNL under contract No. W-7405-Eng-48 and supported by NASA APRA grants to LLNL, GSFC, and Stanford University.

Ultrafast atomic process in X-ray emission by using inner-shell ionization method for sodium and carbon atoms

Energy Technology Data Exchange (ETDEWEB)

Moribayashi, Kengo; Sasaki, Akira; Tajima, Toshiki [Japan Atomic Energy Research Inst., Neyagawa, Osaka (Japan). Kansai Research Establishment

1998-07-01

An ultrafast inner-shell ionization process with X-ray emission stimulated by high-intensity short-pulse X-ray is studied. Carbon and sodium atoms are treated as target matter. It is shown that atomic processes of the target determine the necessary X-ray intensity for X-ray laser emission as well as the features of X-ray laser such as wavelength and duration time. The intensity also depends on the density of initial atoms. Furthermore, we show that as the intensity of X-ray source becomes high, the multi-inner-shell ionization predominates, leading to the formation of hollow atoms. As the density of hollow atoms is increased by the pumping X-ray power, the emission of X-rays is not only of significance for high brightness X-ray measurement but also is good for X-ray lasing. New classes of experiments of pump X-ray probe and X-ray laser are suggested. (author)

Theoretical study of inner-shell ionization by heavy-particle impact

International Nuclear Information System (INIS)

Sarkadi, L.

2000-01-01

Complete text of publication follows. In our previous theoretical studies of inner-shell ionization of atoms by heavy-particle impact we applied the so-called coupled-states model. This theory was constructed to account for the intra-shell coupling effects in L-shell ionization. The model satisfactory reproduced the main tendencies of the measured L-shell ionization data (cross sections, L 3 -subshell alignment parameters) in a broad range of the collision energy, target and projectile atomic number. However, the accuracy of these calculations was uncertain, because the coupled-states model contained a series of approximation. The most questionable assumption was that the changes of the cross sections due to the subshell coupling effects were expressed by correction factors. The correction factors were derived considering only some representative transitions between the bound and continuum states, namely transitions into states of energy E f = 0 and angular momentum l f = 0.1. As a first step to improve the coupled-states model, a computer program was developed to calculate the matrix elements of the Coulomb interaction between a charged particle and an atomic electron, ∫ ψ* f (r) /R - r/ -1 ψ i (r)dr, for arbitrary final state energy E f and angular momentum l f . The ψ k (r)'s are non-relativistic hydrogenic wave functions. The program consists of subroutines that compute matrix elements between eigenstates of both the total angular momentum j, and the orbital angular momentum l. As further output quantities, the radial components of the multipole series expansion of the matrix elements (the so-called G functions) can be obtained, as well. The structure of the program is such that the hydrogenic wave functions can be replaced by arbitrary one-electron wave functions. The program was tested in calculations of K-, L- and M-shell ionization probabilities and cross sections within the framework of the straight-line version of the (first-order) semiclassical

Composites Based on Core-Shell Structured HBCuPc@CNTs-Fe3O4 and Polyarylene Ether Nitriles with Excellent Dielectric and Mechanical Properties

Science.gov (United States)

Pu, Zejun; Zhong, Jiachun; Liu, Xiaobo

2017-10-01

Core-shell structured magnetic carbon nanotubes (CNTs-Fe3O4) coated with hyperbranched copper phthalocyanine (HBCuPc) (HBCuPc@CNTs-Fe3O4) hybrids were prepared by the solvent-thermal method. The results indicated that the HBCuPc molecules were decorated on the surface of CNTs-Fe3O4 through coordination behavior of phthalocyanines, and the CNTs-Fe3O4 core was completely coaxial wrapped by a functional intermediate HBCuPc shell. Then, polymer-based composites with a relatively high dielectric constant and low dielectric loss were fabricated by using core-shell structured HBCuPc@CNTs-Fe3O4 hybrids as fillers and polyarylene ether nitriles (PEN) as the polymer matrix. The cross-sectional scanning electron microscopy (SEM) images of composites showed that there is almost no agglomeration and internal delamination. In addition, the rheological analysis reveals that the core-shell structured HBCuPc@CNTs-Fe3O4 hybrids present better dispersion and stronger interface adhesion with the PEN matrix than CNTs-Fe3O4, thus resulting in significant improvement of the mechanical, thermal and dielectric properties of polymer-based composites.

Implosion dynamics of a megampere wire-array Z-pinch with an inner low-density foam shell at the Angara-5-1 facility

International Nuclear Information System (INIS)

Aleksandrov, V. V.; Bolkhovitinov, E. A.; Volkov, G. S.; Grabovski, E. V.; Gritsuk, A. N.; Medovshchikov, S. F.; Oleinik, G. M.; Rupasov, A. A.; Frolov, I. N.

2016-01-01

The implosion dynamics of a pinch with a highly inhomogeneous initial axial distribution of the load mass was studied experimentally. A cascade array consisting of a double nested tungsten wire array and a coaxial inner cylindrical shell located symmetrically with respect to the high-voltage electrodes was used as a load of the Angara-5-1 high-current generator. The cylindrical foam shell was half as long as the cathode− anode gap, and its diameter was equal to the diameter of the inner wire array. It is shown experimentally that two stages are typical of the implosion dynamics of such a load: the formation of two separate pinches formed as a result of implosion of the wire array near the cathode and anode and the subsequent implosion of the central part of the load containing the cylindrical foam shell. The conditions are determined at which the implosion of the central part of the pinch with the foam cylinder is preceded by intense irradiation of the foam with the soft X-ray (SXR) emission generated by the near-electrode pinches and converting it into the plasma state. Using such a load, which models the main elements of the scheme of a dynamic hohlraum for inertial confinement fusion, it is possible to increase the efficiency of interaction between the outer accelerated plasma sheath and the inner foam shell by preionizing the foam with the SXR emission of the near-electrode pinches.

Ferromagnetic resonance on oxideless magnetic Fe and FeRh nanoparticles; Ferromagnetische Resonanz an oxidfreien magnetischen Fe und FeRh Nanopartikeln

Energy Technology Data Exchange (ETDEWEB)

Trunova, Anastasia

2009-05-25

This work is dedicated to investigations of structural and magnetic properties of the colloidal Fe/Fe{sub x}O{sub y} nanocubes (13 nm) and the Fe{sub x}Rh{sub 100-x} core/shell nanoparticles (2 nm). As compared with other works, where the measurements on oxidized nanoparticles were carried out, we additionally performed investigations on nanoparticles in an oxide free state. In order to make the measurements on oxide free particles possible, oxygen- and hydrogenplasma was used to remove the ligands and reduce the oxide shell of the Fe nanocubes. The oxide free Fe nanocubes were covered with a Ag/Pt protective coating to prevent them from new oxidation. This method allowed carrying out the magnetic measurements on oxide free Fe nanocubes. Micromagnetic simulations as well as simulations of the high frequency susceptibility were used for the data analysing. It was found that both the g-factor g=2.09{+-}0.01 and the anisotropy constant K{sub 4}=(4.8{+-}0.5).10{sup 4} J/m{sup 3} coincide with that of bulk iron. However, the saturation magnetization M{sub S}(5 K)=(1.2{+-}0.12).10{sup 6} A/m differs from the bulk value by 30%. The reduction by 30% compared to the bulk value in the case of nanoparticles may be caused by the following possible reasons: a) the presence of inner oxide layer (approx. 10 at.%) that cannot be reduced; b) the anti-parallel order between magnetic moments of iron core and magnetic moments of antiferomagnetic iron oxide; c) some structural changes of the surface after plasma treatment. The obtained damping parameter {alpha}=0.03{+-}0.005 is ten times larger than that of the Fe layers as it is known for nanoparticles systems in general. The core/shell Fe{sub x}Rh{sub 100-x} nanoparticles (x=80,50) were produced under Ar-atmosphere and were sealed into a quartz tube to prevent oxidation. The analysis of g-factors shows that the value for the FePh nanoparticles with Fe-rich core is larger (g=2.08{+-}0.01) than that for the nanoparticles with Rh

Interchange core/shell assembly of diluted magnetic semiconductor CeO2 and ferromagnetic ferrite Fe3O4 for microwave absorption

Directory of Open Access Journals (Sweden)

Jiaheng Wang

2017-05-01

Full Text Available Core/shell-structured CeO2/Fe3O4 and Fe3O4/CeO2 nanocapsules are prepared by interchange assembly of diluted magnetic semiconductor CeO2 and ferromagnetic ferrite Fe3O4 as the core and the shell, and vice versa, using a facile two-step polar solvothermal method in order to utilize the room-temperature ferromagnetism and abundant O-vacancies in CeO2, the large natural resonance in Fe3O4, and the O-vacancy-enhanced interfacial polarization between CeO2 and Fe3O4 for new generation microwave absorbers. Comparing to Fe3O4/CeO2 nanocapsules, the CeO2/Fe3O4 nanocapsules show an improved real permittivity of 3–10% and an enhanced dielectric resonance of 1.5 times at 15.3 GHz due to the increased O-vacancy concentration in the CeO2 cores of larger grains as well as the O-vacancy-induced enhancement in interfacial polarization between the CeO2 cores and the Fe3O4 shells, respectively. Both nanocapsules exhibit relatively high permeability in the low-frequency S and C microwave bands as a result of the bi-magnetic core/shell combination of CeO2 and Fe3O4. The CeO2/Fe3O4 nanocapsules effectively enhance permittivity and permeability in the high-frequency Ku band with interfacial polarization and natural resonance at ∼15 GHz, thereby improving absorption with a large reflection loss of -28.9 dB at 15.3 GHz. Experimental and theoretical comparisons with CeO2 and Fe3O4 nanoparticles are also made.

Coulomb interaction in atomic and nuclear physics: Inner-Shell excitation, Coulomb dissociation of nuclei, and nuclear polarizability in electronic atoms

International Nuclear Information System (INIS)

Hoffmann, B.

1984-07-01

In three chapters different physical situations are described which have commonly the Coulomb interaction as driving force. The first two chapters study the Coulomb interactions in connection with the excitation of inner electron shells and the Coulomb excitation of nuclei in first order. In the third part on effect ofthe Coulomb interaction between electronic shell and nucleus is treated in second order (nuclear polarization), and its effect on the isotopic and isomeric shift is studied. (orig./HSI) [de

Synthesis and characterization of Fe{sub 3}O{sub 4}–TiO{sub 2} core-shell nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Stefan, M., E-mail: maria.stefan@itim-cj.ro; Pana, O.; Leostean, C.; Silipas, D. [National Institute for R and D of Isotopic and Molecular Technology, 67–103 Donat St., 400295 Cluj-Napoca (Romania); Bele, C. [University of Agricultural Sciences and Veterinary Medicine, 3-5 Calea Mănăştur, 400372 Cluj-Napoca (Romania); Senila, M. [INCDO-INOE 2000, Research Institute for Analytical Instrumentation, 65 Donat St., 400293 Cluj-Napoca (Romania); Gautron, E. [Institute of Materials Jean Rouxel, 2 rue de la Houssière, P.O. Box 32229, 44322 Nantes Cedex 3 (France)

2014-09-21

Composite core-shell nanoparticles may have morpho-structural, magnetic, and optical (photoluminescence (PL)) properties different from each of the components considered separately. The properties of Fe{sub 3}O{sub 4}–TiO{sub 2} nanoparticles can be controlled by adjusting the titania amount (shell thinness). Core–shell nanoparticles were prepared by seed mediated growth of semiconductor (TiO{sub 2}) through a modified sol-gel process onto preformed magnetite (Fe{sub 3}O{sub 4}) cores resulted from the co-precipitation method. The structure and morphology of samples were characterized by X-ray diffraction, transmission electron microscopy (TEM), and high resolution-TEM respectively. X-ray photoelectron spectroscopy was correlated with ICP-AES. Magnetic measurements, optical absorption spectra, as well as PL spectroscopy indicate the presence of a charge/spin transfer from the conduction band of magnetite into the band gap of titania nanocrystals. The process modifies both Fe{sub 3}O{sub 4} and TiO{sub 2} magnetic and optical properties, respectively.

DFT study of Fe-Ni core-shell nanoparticles: Stability, catalytic activity, and interaction with carbon atom for single-walled carbon nanotube growth

International Nuclear Information System (INIS)

Yang, Zhimin; Wang, Qiang; Shan, Xiaoye; Zhu, Hongjun; Li, Wei-qi; Chen, Guang-hui

2015-01-01

Metal catalysts play an important role in the nucleation and growth of single-walled carbon nanotubes (SWCNTs). It is essential for probing the nucleation and growth mechanism of SWCNTs to fundamentally understand the properties of the metal catalysts and their interaction with carbon species. In this study, we systematically studied the stability of 13- and 55-atom Fe and Fe-Ni core-shell particles as well as these particles interaction with the carbon atoms using the density functional theory calculations. Icosahedral 13- and 55-atom Fe-Ni core-shell bimetallic particles have higher stability than the corresponding monometallic Fe and Ni particles. Opposite charge transfer (or distribution) in these particles leads to the Fe surface-shell displays a positive charge, while the Ni surface-shell exhibits a negative charge. The opposite charge transfer would induce different chemical activities. Compared with the monometallic Fe and Ni particles, the core-shell bimetallic particles have weaker interaction with C atoms. More importantly, C atoms only prefer staying on the surface of the bimetallic particles. In contrast, C atoms prefer locating into the subsurface of the monometallic particles, which is more likely to form stable metal carbides. The difference of the mono- and bimetallic particles on this issue may result in different nucleation and growth mechanism of SWCNTs. Our findings provide useful insights for the design of bimetallic catalysts and a better understanding nucleation and growth mechanism of SWCNTs

Preparation of Multifunctional Fe@Au Core-Shell Nanoparticles with Surface Grafting as a Potential Treatment for Magnetic Hyperthermia.

Science.gov (United States)

Chung, Ren-Jei; Shih, Hui-Ting

2014-01-24

Iron core gold shell nanoparticles grafted with Methotrexate (MTX) and indocyanine green (ICG) were synthesized for the first time in this study, and preliminarily evaluated for their potential in magnetic hyperthermia treatment. The core-shell Fe@Au nanoparticles were prepared via the microemulsion process and then grafted with MTX and ICG using hydrolyzed poly(styrene-alt-maleic acid) (PSMA) to obtain core-shell Fe@Au-PSMA-ICG/MTX nanoparticles. MTX is an anti-cancer therapeutic, and ICG is a fluorescent dye. XRD, TEM, FTIR and UV-Vis spectrometry were performed to characterize the nanoparticles. The data indicated that the average size of the nanoparticles was 6.4 ± 09 nm and that the Au coating protected the Fe core from oxidation. MTX and ICG were successfully grafted onto the surface of the nanoparticles. Under exposure to high frequency induction waves, the superparamagnetic nanoparticles elevated the temperature of a solution in a few minutes, which suggested the potential for an application in magnetic hyperthermia treatment. The in vitro studies verified that the nanoparticles were biocompatible; nonetheless, the Fe@Au-PSMA-ICG/MTX nanoparticles killed cancer cells (Hep-G2) via the magnetic hyperthermia mechanism and the release of MTX.

Contribution of inner shell electrons to position-dependent stopping powers of a crystal surface

International Nuclear Information System (INIS)

Narumi, Kazumasa; Fujii, Yoshikazu; Kishine, Keiji; Kurakake, Hiroshi; Kimura, Kenji; Mannami, Michi-hiko

1994-01-01

Position-dependent stopping powers of the (001) surface of SnTe single crystal for specularly reflected 15 - 200 keV H + ions are studied. The position dependence of the experimental stopping powers varies with the energy of ions. From the comparison with the theoretical stopping powers based on both the single ion-electron collision and the collective excitation of the valence electrons, it is concluded that the observed change in the position-dependent stopping powers with energy of H + is due to the variation of contribution of inner shell electrons to stopping. (author)

High resolution inner-shell spectroscopies of atoms and molecules in gas phase using the soft x-ray photochemistry beamline at SPring-8

International Nuclear Information System (INIS)

Ueda, Kiyoshi

2003-01-01

This article describes recent activities on inner-shell spectroscopies of atoms and molecules on beamline 27SU, nicknamed soft X-ray photochemistry beamline, at SPring-8, an 8-GeV synchrotron radiation facility in Japan. This beamline provides linearly polarized monochromatic soft X-rays at the resolution higher than 10,000. The end station is designed so that one can perform various kinds of excitation and de-excitation spectroscopies as well as coincidence spectroscopies. Following the description of the beamline and the end station, we present recent results for inner-shell spectroscopies on Ne, CO 2 , BF 3 , and CF 4 . Emphasis is given to illustrate the strategy of the research on this beamline and performance of the beamline and the end station. (author)

Enhancement of Fenton processes at initial circumneutral pH for the degradation of norfloxacin with Fe@Fe2O3 core-shell nanomaterials.

Science.gov (United States)

Liu, Jingyi; Hu, Wenyong; Sun, Maogui; Xiong, Ouyang; Yu, Haibin; Feng, Haopeng; Wu, Xuan; Tang, Lin; Zhou, Yaoyu

2018-06-13

The degradation of norfloxacin by Fenton reagent with core-shell Fe@Fe 2 O 3 nanomaterials was studied under neutral conditions in a closed batch system. Norfloxacin was significantly degraded (90%) in the Fenton system with Fe@Fe 2 O 3 in 30 min at the initial pH 7.0, but slightly degraded in Fenton system without Fe@Fe 2 O 3 under the same experimental conditions. The intermediate products were investigated by gas chromatography-mass spectrometry, and the possible Fenton oxidation pathway of norfloxacin in the presence of Fe@Fe 2 O 3 nanowires was proposed. Electron spin resonance spectroscopy was used to identify and characterize the free radicals generated, and the mechanism for norfloxacin degradation was also revealed. Finally, the reusability and the stability of Fe@Fe 2 O 3 nanomaterials were studied using x-ray diffraction and scanning electron microscope, which indicated that Fe@Fe 2 O 3 is a stable catalyst and can be used repetitively in environmental pollution control.

Core@shell@shell structured carbon-based magnetic ternary nanohybrids: Synthesis and their enhanced microwave absorption properties

Science.gov (United States)

Yang, Erqi; Qi, Xiaosi; Xie, Ren; Bai, Zhongchen; Jiang, Yang; Qin, Shuijie; Zhong, Wei; Du, Youwei

2018-05-01

High encapsulation efficiency of core@shell@shell structured carbon-based magnetic ternary nanohybrids have been synthesized in high yield by chemical vapor deposition of acetylene directly over octahedral-shaped Fe2O3 nanoparticles. By controlling the pyrolysis temperature, Fe3O4@Fe3C@carbon nanotubes (CNTs) and Fe@Fe3C@CNTs ternary nanohybrids could be selectively produced. The optimal RL values for the as-prepared ternary nanohybrids could reach up to ca. -46.7, -52.7 and -29.5 dB, respectively. The excellent microwave absorption properties of the obtaiend ternary nanohybrids were proved to ascribe to the quarter-wavelength matching model. Moreover, the as-prepared Fe@Fe3C@CNTs ternary nanohybrids displayed remarkably enhanced EM wave absorption capabilities compared to Fe3O4@Fe3C@CNTs due to their excellent dielectric loss abilities, good complementarities between the dielectric loss and the magnetic loss, and high attenuation constant. Generally, this strategy can be extended to explore other categories of core@shell or core@shell@shell structured carbon-based nanohybrids, which is very beneficial to accelerate the advancements of high performance MAMs.

Preparation of Multifunctional Fe@Au Core-Shell Nanoparticles with Surface Grafting as a Potential Treatment for Magnetic Hyperthermia

Directory of Open Access Journals (Sweden)

Ren-Jei Chung

2014-01-01

Full Text Available Iron core gold shell nanoparticles grafted with Methotrexate (MTX and indocyanine green (ICG were synthesized for the first time in this study, and preliminarily evaluated for their potential in magnetic hyperthermia treatment. The core-shell Fe@Au nanoparticles were prepared via the microemulsion process and then grafted with MTX and ICG using hydrolyzed poly(styrene-alt-maleic acid (PSMA to obtain core-shell Fe@Au-PSMA-ICG/MTX nanoparticles. MTX is an anti-cancer therapeutic, and ICG is a fluorescent dye. XRD, TEM, FTIR and UV-Vis spectrometry were performed to characterize the nanoparticles. The data indicated that the average size of the nanoparticles was 6.4 ± 09 nm and that the Au coating protected the Fe core from oxidation. MTX and ICG were successfully grafted onto the surface of the nanoparticles. Under exposure to high frequency induction waves, the superparamagnetic nanoparticles elevated the temperature of a solution in a few minutes, which suggested the potential for an application in magnetic hyperthermia treatment. The in vitro studies verified that the nanoparticles were biocompatible; nonetheless, the Fe@Au-PSMA-ICG/MTX nanoparticles killed cancer cells (Hep-G2 via the magnetic hyperthermia mechanism and the release of MTX.

Fe3O4@polyaniline yolk-shell micro/nanospheres as bifunctional materials for lithium storage and electromagnetic wave absorption

Science.gov (United States)

Wang, Xiaoliang; Zhang, Minwei; Zhao, Jianming; Huang, Guoyong; Sun, Hongyu

2018-01-01

Unique Fe3O4/polyaniline (PANI) composite with yolk-shell micro/nanostructure (FPys) has been successfully synthesized by a facile silica-assisted in-situ polymerization and subsequent etching strategy. The structural and compositional studies of the FPys composites are performed by employing X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The yolk-shell morphology of the products is confirmed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) observations. When evaluated as anode material for lithium-ion batteries, the as-prepared FPys electrodes deliver superior capacity, better cycling stability and rate capability than those of bare Fe3O4 micro/nanospheres and Fe3O4/PANI core-shell (FPcs) electrodes. Moreover, FPys also exhibits excellent electromagnetic wave absorption performance when comparing to the synthesized Fe3O4-based electromagnetic wave absorbers, in which strong reflection loss and extensive response bandwidth can be achieved simultaneously. The excellent bifunctional properties of FPys material are associated with the specially designed hierarchical micro/nanostructures. The current strategy that application directed structural design can be applied to the synthesis of other multifunctional materials.

FE-Simulation Of Hemming In The Automotive Industry

International Nuclear Information System (INIS)

Sigvant, Mats; Mattiasson, Kjell

2005-01-01

This paper summarizes and presents the most important results from a research project on FE simulation of hemming carried out at Volvo Cars Body Components and Chalmers University of Technology. In the automotive industry, hemming is used to join two sheet metal panels by bending the flange of the outer panel over the inner one. The final goal of the project was to simulate all of the hemming steps of production parts. In order to make three-dimensional simulations of hemming possible within reasonable simulation times, it is necessary to use shell elements and not solid elements. On the other hand, the radius of curvature of the outer part in the folded area is very small, normally of the same order of magnitude as the sheet thickness. This fact raises the question if shell elements are applicable in FE simulation of hemming. One part of the project was therefore a thorough investigation of the order of magnitude of the errors resulting from the use of shell elements in FE simulation of hemming. Another part of the project was devoted to three-dimensional simulations of the hemming of an automotive hood. The influence on the roll-in from several parameters, such as shell element formulation, adhesives, and anisotropy was studied. Finally, results from a forming simulation were also mapped to the flanging and hemming models in order to study the influence from the stamping of the outer panel on the roll-in

Chemical synthesis of Fe/Fe{sub 3}O{sub 4} core-shell composites with enhanced soft magnetic performances

Energy Technology Data Exchange (ETDEWEB)

Yang, Bai, E-mail: byang@buaa.edu.cn [Key Laboratory of Aerospace Advanced Materials and Performance, Ministry of Education, School of Materials Science and Engineering, Beihang University, Beijing 100191 (China); Li, Xiaopan [Key Laboratory of Aerospace Advanced Materials and Performance, Ministry of Education, School of Materials Science and Engineering, Beihang University, Beijing 100191 (China); Yang, Xueying [Hi-tech Industry Standardization Institute, Hubei Standardization and Quality Institution, Wuhan 430061 (China); Yu, Ronghai [Key Laboratory of Aerospace Advanced Materials and Performance, Ministry of Education, School of Materials Science and Engineering, Beihang University, Beijing 100191 (China)

2017-04-15

The large-grain Fe/Fe{sub 3}O{sub 4} composite particles with average size of about 1.2 µm have been fabricated by a facile one-step solvothermal method. The formation of high-purity Fe{sub 3}O{sub 4} as the shells (90.14 wt%) and α-Fe as the cores (9.86 wt%) in the Fe/Fe{sub 3}O{sub 4} composites leads to their high saturation magnetization of 119.6 A m{sup 2} Kg{sup -1}. Very low coercivity of 30 Oe is obtained in the composites due to their uniform cubic-shaped morphologies. Compared with Fe-based nanosized particles, these micron-sized magnetic Fe/Fe{sub 3}O{sub 4} composites exhibit high air stability and good compactibility with high compressed density of 5.9 g cm{sup -3}. The fully compacted sample shows good soft magnetic properties including high magnetic induction B{sub 1.2k} {sub (H=1200} {sub A/m)} of 540 mT and good frequency-dependent magnetic properties with operating frequency up to 50 MHz superior to those of the most traditional soft magnetic ferrites, which promotes their potential applications in high-frequency and high-power magnetic devices. - Highlights: • Micron-sized Fe/Fe{sub 3}O{sub 4} composites are prepared by a one-step solvothermal method. • High saturation magnetization and low coercivity are obtained in the composites. • Good air stability and high bulk density occurs in the composites. • High magnetic induction and good frequency-dependent properties are achieved.

A GREENER SYNTHESIS OF CORE (FE, CU)-SHELL (AU, PT, PD AND AG) NANOCRYSTALS USING AQUEOUS VITAMIN C

Science.gov (United States)

A greener method to fabricate the novel core (Fe and Cu)-shell (noble metals) metal nanocrystals using aqueous ascorbic acid (vitamin C) is described. Transition metal salts such as Cu and Fe were reduced using ascorbic acid, a benign naturally available antioxidant, and then add...

Role of N-methyl-2-pyrrolidone for preparation of Fe{sub 3}O{sub 4}@SiO{sub 2} controlled the shell thickness

Energy Technology Data Exchange (ETDEWEB)

Wee, Sung-Bok [Hanyang University, Division of Materials Science and Engineering (Korea, Republic of); Oh, Hyeon-Cheol [Korea Nano Plus, Inc. (Korea, Republic of); Kim, Tae-Gyun; An, Gye-Seok; Choi, Sung-Churl, E-mail: choi0505@hanyang.ac.kr [Hanyang University, Division of Materials Science and Engineering (Korea, Republic of)

2017-04-15

We developed a simple and novel approach for the synthesis of Fe{sub 3}O{sub 4}@SiO{sub 2} nanoparticles with controlled shell thickness, and studied the mechanism. The introduction of N-methyl-2-pyrrolidone (NMP) led to trapping of monomer nuclei in single shell and controlled the shell thickness. Fe{sub 3}O{sub 4}@SiO{sub 2} controlled the shell thickness, showing a high magnetization value (64.47 emu/g). Our results reveal the role and change in the chemical structure of NMP during the core-shell synthesis process. NMP decomposed to 4-aminobutanoic acid in alkaline condition and decreased the hydrolysis rate of the silica coating process.

Preparation and photocatalytic properties of hybrid core–shell reusable CoFe2O4–ZnO nanospheres

International Nuclear Information System (INIS)

Wilson, A.; Mishra, S.R.; Gupta, R.; Ghosh, K.

2012-01-01

Magnetically separable and reusable core–shell CoFe 2 O 4 –ZnO photocatalyst nanospheres were prepared by the hydrothermal synthesis technique using glucose derived carbon nanospheres as the template. The morphology and the phase of core–shell hybrid structure of CoFe 2 O 4 –ZnO were assessed via TEM, SEM and XRD. The magnetic composite showed high UV photocatalytic activity for the degradation of methylene blue in water. The photocatalytic activity was found to be ZnO shell thickness dependent. Thicker ZnO shells lead to higher rate of photocatalytic activity. Hybrid nanospheres recovered using an external magnetic field demonstrated good repeatability of photocatalytic activity. These results promise the reusability of the hybrid nanospheres for photocatalytic activity. - Highlights: ► Synthesis of novel hybrid magnetic-ZnO core–shell composite nanospheres. ► High photocatalytic activity of hybrid nanospheres was noted as compared to that of pure ZnO nanoparticles. ► The hybrid nanospheres could be easily retrieved using an external magnet for repeated use. ► Repeated use of hybrid nanospheres did not show any degradation in the photocatalytic activity. ► The photocatalysis rate was observed to be ZnO shell thickness dependent.

Ferromagnetic resonance on oxideless magnetic Fe and FeRh nanoparticles

International Nuclear Information System (INIS)

Trunova, Anastasia

2009-01-01

This work is dedicated to investigations of structural and magnetic properties of the colloidal Fe/Fe x O y nanocubes (13 nm) and the Fe x Rh 100-x core/shell nanoparticles (2 nm). As compared with other works, where the measurements on oxidized nanoparticles were carried out, we additionally performed investigations on nanoparticles in an oxide free state. In order to make the measurements on oxide free particles possible, oxygen- and hydrogenplasma was used to remove the ligands and reduce the oxide shell of the Fe nanocubes. The oxide free Fe nanocubes were covered with a Ag/Pt protective coating to prevent them from new oxidation. This method allowed carrying out the magnetic measurements on oxide free Fe nanocubes. Micromagnetic simulations as well as simulations of the high frequency susceptibility were used for the data analysing. It was found that both the g-factor g=2.09±0.01 and the anisotropy constant K 4 =(4.8±0.5).10 4 J/m 3 coincide with that of bulk iron. However, the saturation magnetization M S (5 K)=(1.2±0.12).10 6 A/m differs from the bulk value by 30%. The reduction by 30% compared to the bulk value in the case of nanoparticles may be caused by the following possible reasons: a) the presence of inner oxide layer (approx. 10 at.%) that cannot be reduced; b) the anti-parallel order between magnetic moments of iron core and magnetic moments of antiferomagnetic iron oxide; c) some structural changes of the surface after plasma treatment. The obtained damping parameter α=0.03±0.005 is ten times larger than that of the Fe layers as it is known for nanoparticles systems in general. The core/shell Fe x Rh 100-x nanoparticles (x=80,50) were produced under Ar-atmosphere and were sealed into a quartz tube to prevent oxidation. The analysis of g-factors shows that the value for the FePh nanoparticles with Fe-rich core is larger (g=2.08±0.01) than that for the nanoparticles with Rh-rich core and coincides within error bars with the g-factor of bulk

The role of interfacial metal silicates on the magnetism in FeCo/SiO{sub 2} and Fe{sub 49%}Co{sub 49%}V{sub 2%}/SiO{sub 2} core/shell nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Desautels, R. D., E-mail: rddesautels@physics.umanitoba.ca [Department of Physics and Astronomy, University of Manitoba, Winnipeg, Manitoba R3T 2N2 (Canada); Toyota Research Institute of North America, Ann Arbor, Michigan 48169 (United States); Freeland, J. W. [Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois 60439 (United States); Rowe, M. P. [Toyota Research Institute of North America, Ann Arbor, Michigan 48169 (United States); Lierop, J. van [Department of Physics and Astronomy, University of Manitoba, Winnipeg, Manitoba R3T 2N2 (Canada)

2015-05-07

We have investigated the role of spontaneously formed interfacial metal silicates on the magnetism of FeCo/SiO{sub 2} and Fe{sub 49%}Co{sub 49%}V{sub 2%}/SiO{sub 2} core/shell nanoparticles. Element specific x-ray absorption and photoelectron spectroscopy experiments have identified the characteristic spectral features of metallic iron and cobalt from within the nanoparticle core. In addition, metal silicates of iron, cobalt, and vanadium were found to have formed spontaneously at the interface between the nanoparticle core and silica shell. X-ray magnetic circular dichroism experiments indicated that the elemental magnetism was a result of metallic iron and cobalt with small components from the iron, cobalt, and vanadium silicates. Magnetometry experiments have shown that there was no exchange bias loop shift in the FeCo nanoparticles; however, exchange bias from antiferromagnetic vanadium oxide was measured in the V-doped nanoparticles. These results showed clearly that the interfacial metal silicates played a significant role in the magnetism of these core/shell nanoparticles, and that the vanadium percolated from the FeCo-cores into the SiO{sub 2}-based interfacial shell.

Decay energy of 55Fe from its inner Bremsstrahlung spectrum

Science.gov (United States)

Keshava, S. L.; Gopala, K.; Venkataramaiah, P.

2001-06-01

Several measurements of decay energy using the inner Bremsstrahlung spectrum (IB) due to radiative electron capture in 55Fe has been made. But the results are not uniform. Hence another attempt has been made at the same. Experimental data was obtained with a 4.445 cm. dia ' 5.08 cm thick NaI (Tl) detector. It was subjected to suitable statistical treatment and various corrections using Liden and Starfelt procedure. The corrected spectrum agrees well with the Glauber and Martin theory for 1s electron capture beyond 100 keV. From the Jauch plot, the decay energy of 232.36 +/-0.64 keV was obtained.

Decay energy of 55Fe from its inner Bremsstrahlung spectrum

International Nuclear Information System (INIS)

Keshava, S.L.; Gopala, K.; Venkataramaiah, P.

2001-01-01

Several measurements of decay energy using the inner Bremsstrahlung spectrum (IB) due to radiative electron capture in 55 Fe has been made. But the results are not uniform. Hence another attempt has been made at the same. Experimental data was obtained with a 4.445 cm dia x 5.08 cm thick NaI (Tl) detector. It was subjected to suitable statistical treatment and various corrections using Liden and Starfelt procedure. The corrected spectrum agrees well with the Glauber and Martin theory for l s electron capture beyond 100 keV. From the Jauch plot, the decay energy of 232.36±0.64 keV was obtained. (author)

Study of surface by ion scattering with simultaneous formation of inner shell vacancies

International Nuclear Information System (INIS)

Zinov'ev, A.N.

2002-01-01

The program on modeling the atomic particles scattering, making it possible to account for the change in the particles charge state in each collision act with an account of the additional ionization, is developed. It is shown, that the additional ionization of the departing particles due to the decay of vacancies in the inner shells increases the accuracy of the surface composition analysis. The algorithm of deriving from the experimental data the information on the dependence of the particles neutralization probability on the distance from the surface is proposed and the conclusion is made on the necessity of accounting for the recharge process for neutralization of the ions with the q>2 [ru

Reverse-Engineering Laboratory Astrophysics: Oxygen Inner-shell Absorption in the ISM

Science.gov (United States)

Garcia, J.; Gatuzz, E.; Kallman, T. R.; Mendoza, C.; Gorczyca, T. W.

2017-01-01

The modeling of X-ray spectra from photoionized astrophysical plasmas has been significantly improved due to recent advancements in the theoretical and numerical frameworks, as well as a consolidated and reliable atomic database of inner-shell transitions for all the relevant ions. We discuss these developments and the current state of X-ray spectral modeling in the context of oxygen cold absorption in the interstellar medium (ISM). Unconventionally, we use high-resolution astrophysical observations to accurately determine line positions, and adjust the theoretical models for a comprehensive interpretation of the observed X-ray spectra. This approach has brought to light standing discrepancies in the neutral oxygen absorption-line positions determined from observations and laboratory measurements. We give an overview of our current efforts to devise a definitive model of oxygen photoabsorption that can help to resolve the existing controversy regarding ISM atomic and molecular fractions.

Synthesis of Co/MFe(2)O(4) (M = Fe, Mn) Core/Shell Nanocomposite Particles.

Science.gov (United States)

Peng, Sheng; Xie, Jin; Sun, Shouheng

2008-01-01

Monodispersed cobalt nanoparticles (NPs) with controllable size (8-14 nm) have been synthesized using thermal decomposition of dicobaltoctacarbonyl in organic solvent. The as-synthesized high magnetic moment (125 emu/g) Co NPs are dispersible in various organic solvents, and can be easily transferred into aqueous phase by surface modification using phospholipids. However, the modified hydrophilic Co NPs are not stable as they are quickly oxidized, agglomerated in buffer. Co NPs are stabilized by coating the MFe(2)O(4) (M = Fe, Mn) ferrite shell. Core/shell structured bimagnetic Co/MFe(2)O(4) nanocomposites are prepared with tunable shell thickness (1-5 nm). The Co/MFe(2)O(4) nanocomposites retain the high magnetic moment density from the Co core, while gaining chemical and magnetic stability from the ferrite shell. Comparing to Co NPs, the nanocomposites show much enhanced stability in buffer solution at elevated temperatures, making them promising for biomedical applications.

Preparation and photocatalytic properties of hybrid core-shell reusable CoFe{sub 2}O{sub 4}-ZnO nanospheres

Energy Technology Data Exchange (ETDEWEB)

Wilson, A. [Department of Physics, University of Memphis, Memphis, TN 38152 (United States); Mishra, S.R., E-mail: srmishra@memphis.edu [Department of Physics, University of Memphis, Memphis, TN 38152 (United States); Gupta, R.; Ghosh, K. [Department of Physics, Materials Science, and Astronomy, Missouri State University, Springfield, MO (United States)

2012-08-15

Magnetically separable and reusable core-shell CoFe{sub 2}O{sub 4}-ZnO photocatalyst nanospheres were prepared by the hydrothermal synthesis technique using glucose derived carbon nanospheres as the template. The morphology and the phase of core-shell hybrid structure of CoFe{sub 2}O{sub 4}-ZnO were assessed via TEM, SEM and XRD. The magnetic composite showed high UV photocatalytic activity for the degradation of methylene blue in water. The photocatalytic activity was found to be ZnO shell thickness dependent. Thicker ZnO shells lead to higher rate of photocatalytic activity. Hybrid nanospheres recovered using an external magnetic field demonstrated good repeatability of photocatalytic activity. These results promise the reusability of the hybrid nanospheres for photocatalytic activity. - Highlights: Black-Right-Pointing-Pointer Synthesis of novel hybrid magnetic-ZnO core-shell composite nanospheres. Black-Right-Pointing-Pointer High photocatalytic activity of hybrid nanospheres was noted as compared to that of pure ZnO nanoparticles. Black-Right-Pointing-Pointer The hybrid nanospheres could be easily retrieved using an external magnet for repeated use. Black-Right-Pointing-Pointer Repeated use of hybrid nanospheres did not show any degradation in the photocatalytic activity. Black-Right-Pointing-Pointer The photocatalysis rate was observed to be ZnO shell thickness dependent.

Plasma-assisted synthesis and study of structural and magnetic properties of Fe/C core shell

Science.gov (United States)

Shinde, K. P.; Ranot, M.; Choi, C. J.; Kim, H. S.; Chung, K. C.

2017-07-01

Pure and carbon-encapsulated iron nanoparticles with an average diameter of 25 nm were synthesized by using the DC plasma arc discharge method. Fe core nanoparticles were encapsulated with carbon layer, which is acting as protection layer against both oxidation and chemical reaction. The morphology and the Fe/C core/shell structure of the nanoparticles were studied by using field emission scanning electron microscopy and transmission electron microscopy. The x-ray diffraction study showed that the α-Fe phase exists with γ-Fe as an impurity. The studied samples have been interrelated with the variation of saturation magnetization, remanent magnetization and coercive field with the amount of carbon coating. The pure α-Fe sample shows saturation magnetization = 172 emu/g, and coercive field = 150 Oe, on the other hand few layer carbon coated α-Fe sample shows saturation magnetization =169 emu/g with higher coercive field 398 Oe.

Plasma-assisted synthesis and study of structural and magnetic properties of Fe/C core shell

Directory of Open Access Journals (Sweden)

K. P. Shinde

2017-07-01

Full Text Available Pure and carbon-encapsulated iron nanoparticles with an average diameter of 25 nm were synthesized by using the DC plasma arc discharge method. Fe core nanoparticles were encapsulated with carbon layer, which is acting as protection layer against both oxidation and chemical reaction. The morphology and the Fe/C core/shell structure of the nanoparticles were studied by using field emission scanning electron microscopy and transmission electron microscopy. The x-ray diffraction study showed that the α-Fe phase exists with γ-Fe as an impurity. The studied samples have been interrelated with the variation of saturation magnetization, remanent magnetization and coercive field with the amount of carbon coating. The pure α-Fe sample shows saturation magnetization = 172 emu/g, and coercive field = 150 Oe, on the other hand few layer carbon coated α-Fe sample shows saturation magnetization =169 emu/g with higher coercive field 398 Oe.

Nanosized yolk–shell Fe{sub 3}O{sub 4}@Zr(OH){sub x} spheres for efficient removal of Pb(II) from aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Pan, Shunlong [Jiangsu Key Laboratory of Chemical Pollution Control and Resources Reuse, School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing 210094 (China); Li, Jiansheng, E-mail: lijsh@mail.njust.edu.cn [Jiangsu Key Laboratory of Chemical Pollution Control and Resources Reuse, School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing 210094 (China); Wan, Gaojie; Liu, Chao [Jiangsu Key Laboratory of Chemical Pollution Control and Resources Reuse, School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing 210094 (China); Fan, Wenhong, E-mail: fanwh@buaa.edu.cn [Department of Environmental Science and Engineering, School of Chemistry and Environment, Beihang University, Beijing 100191 (China); Wang, Lianjun, E-mail: wanglj@mail.njust.edu.cn [Jiangsu Key Laboratory of Chemical Pollution Control and Resources Reuse, School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing 210094 (China)

2016-05-15

Highlights: • Well dispersed and easy separated nanoadsorbents with stable chemical property are highly desired. • Fe{sub 3}O{sub 4}@Zr(OH){sub x} yolk–shell nanospheres (YSNs) nanoadsorbents were prepared. • Enhanced Pb(II) adsorption capacity of 310.8 mg/g was achieved on Fe{sub 3}O{sub 4}@Zr(OH){sub x} YSNs based on Zr weight. • The cavities in Fe{sub 3}O{sub 4}@Zr(OH){sub x} YSNs is responsible for the improved performance. - Abstract: In this work, Fe{sub 3}O{sub 4}@Zr(OH){sub x} yolk–shell nanospheres (YSNs) were synthesized via a two-step process and further examined as adsorbents for the removal of Pb(II). To understand the hollow structure on the adsorption properties of Pb(II), another adsorbent without hollow cavities, i.e., Fe{sub 3}O{sub 4}@SiO{sub 2}@Zr(OH){sub x} core–shell nanospheres (CSNs), was also prepared for comparison. The adsorption results showed that Fe{sub 3}O{sub 4}@Zr(OH){sub x} YSNs exhibited 41.6% higher Pb(II) adsorption capacity as compared to that of Fe{sub 3}O{sub 4}@SiO{sub 2}@Zr(OH){sub x} CSNs. The isotherm was well fitted to Langmuir adsorption model with q{sub max} value of 310.8 mg/g after normalized by the weight of Zr in Fe{sub 3}O{sub 4}@Zr(OH){sub x} YSNs. Scanning transmission electron microscopy (STEM) mapping results revealed that the existence of cavities between Fe{sub 3}O{sub 4} cores and Zr(OH){sub x} shells is responsible for the improved adsorption performance. XPS analysis indicated the surface hydroxyl groups played a key role in the Pb(II) adsorption. The removal efficiency of Pb(II) was maintained above 90% in five consecutive adsorption–desorption cycles.

Reduced graphene oxide wrapped Fe3O4-Co3O4 yolk-shell nanostructures for advanced catalytic oxidation based on sulfate radicals

Science.gov (United States)

Zhang, Lishu; Yang, Xijia; Han, Erfen; Zhao, Lijun; Lian, Jianshe

2017-02-01

In this work, we designed and synthesized a high performance catalyst of reduced graphene oxide (RGO) wrapped Fe3O4-Co3O4 (RGO/Fe3O4-Co3O4) yolk-shell nanostructures for advanced catalytic oxidation based on sulfate radicals. The synergistic catalytic action of the RGO/Fe3O4-Co3O4 yolk-shell nanostructures activate the peroxymonosulfate (PMS) to produce sulfate radicals (SO4rad -) for organic dyes degradation, and the Orange II can be almost completely degradated in 5 min. Meanwhile the RGO wrapping prevents the loss of cobalt in the catalytic process, and the RGO/Fe3O4-Co3O4 can be recycled after catalyzed reaction due to the presence of magnetic iron core. What's more, it can maintain almost the same high catalytic activity even after 10 cycles through repeated NaBH4 reduction treatment. Hence, RGO/Fe3O4-Co3O4 yolk-shell nanostructures possess a great opportunity to become a promising candidate for waste water treatment in industry.

Visible and IR photoluminescence of c-FeSi@a–Si core–shell nano-fibres produced by vapour transport

Energy Technology Data Exchange (ETDEWEB)

Thabethe, Sibongiseni [DST/CSIR National Centre for Nano-Structured Materials, PO Box 395, Pretoria 0001 (South Africa); Department of Physics, University of the Western Cape, Private Bag X17, Bellville 7535 (South Africa); Linganiso, Ella; Motaung, David; Mashapa, Matete G.; Nkosi, Steven [DST/CSIR National Centre for Nano-Structured Materials, PO Box 395, Pretoria 0001 (South Africa); Arendse, Christopher J. [Department of Physics, University of the Western Cape, Private Bag X17, Bellville 7535 (South Africa); Mwakikunga, Bonex W., E-mail: bmwakikunga@csir.co.za [DST/CSIR National Centre for Nano-Structured Materials, PO Box 395, Pretoria 0001 (South Africa); Department of Physics and Biochemical Sciences, University of Malawi, The Polytechnic, Private Bag 303, Chichiri, Blantyre 3 (Malawi)

2013-11-15

The procedures for the synthesis of amorphous ε-FeSi/Si core–shell nanofibres by vapour transport in a CVD configuration are reported. Crystallite studies by the Williamson-Hall method show the sizes to be typically about 8.0 nm which agrees with TEM value of 7.9 nm fibre diameter with a compressive strain of about 0.04. Features in the photoluminescence of these FeSi core–shells in both visible and IR are at 410 nm, 1062 nm, 1414 nm and 1772 nm and absorption feature at 1000 cm{sup −1} from FTIR are explained from density functional theory (DFT) ab initio calculations. PL confirms the intra-band transition whereas FTIR agrees perfectly with the band-to-band transition whose band gap energy is 0.13 eV for FeSi. FTIR also unveils inter-band transition which DFT calculation could not predict. Raman spectroscopy data confirm FeSi and nano-Si presence. -- Highlights: • New PL data has been obtained for the c-FeSi@a–Si nano-fibres in the range (0.7–3.1 eV). • FTIR unveils the band-to-band transition within this narrow band gap FeSi. • The new data are explained through electronic energy band structure and density of states of FeSi. • Intra-band transitions as well as quantum confinement are responsible for blue shifts.

High-temperature strength of Nb-1%Zr alloy for irradiation-capsules inner-shell

International Nuclear Information System (INIS)

Nomura, Yasushi; Nakata, Hirokatsu; Tanaka, Mitsuo; Fukaya, Kiyoshi.

1978-04-01

Coated fuel particles in capsules will be irradiated at about 1600 0 C in JMTR. Nb-1%Zr alloy was chosen for inner shell material of the capsules because of its sufficient strength at 1000 0 C and low induced radioactivity. Nb-1%Zr ingot produced by electron beam melting was formed into seamless tubes by hollowing and swaging, followed by annealing. Creep test in helium flow and tensile test in vacuum were made to examine mechanical strength of the Nb-1%Zr tubes at 1000 0 C. Following are the results; 1) 0.2% yield stress at 1000 0 C is about 6 kg/mm 2 . 2) 3000 hr creep rupture stress at 1000 0 C is about 6 kg/mm 2 . (auth.)

Rate of Iron Transfer Through the Horse Spleen Ferritin Shell Determined by the Rate of Formation of Prussian Blue and Fe-desferrioxamine Within the Ferritin Cavity

Science.gov (United States)

Zhang, Bo; Watt, Richard K.; Galvez, Natividad; Dominquez-Vera, Jose M.; Watt, Gerald D.

2005-01-01

Iron (2+ and 3+) is believed to transfer through the three-fold channels in the ferritin shell during iron deposition and release in animal ferritins. However, the rate of iron transit in and out through these channels has not been reported. The recent synthesis of [Fe(CN)(sub 6)](3-), Prussian Blue (PB) and desferrioxamine (DES) all trapped within the horse spleen ferritin (HoSF) interior makes these measurements feasible. We report the rate of Fe(2+) penetrating into the ferritin interior by adding external Fe(2+) to [Fe(CN)(sub 6)](3-) encapsulated in the HoSF interior and measuring the rate of formation of the resulting encapsulated PB. The rate at which Fe(2+) reacts with [Fe(CN)(sub 6)](3-) in the HoSF interior is much slower than the formation of free PB in solution and is proceeded by a lag period. We assume this lag period and the difference in rate represent the transfer of Fe(2+) through the HoSF protein shell. The calculated diffusion coefficient, D approx. 5.8 x 10(exp -20) square meters per second corresponds to the measured lag time of 10-20 s before PB forms within the HoSF interior. The activation energy for Fe(2+) transfer from the outside solution through the protein shell was determined to be 52.9 kJ/mol by conducting the reactions at 10 to approximately 40 C. The reaction of Fe(3+) with encapsulated [Fe(CN)6](4-) also readily forms PB in the HoSF interior, but the rate is faster than the corresponding Fe(2+) reaction. The rate for Fe(3+) transfer through the ferritin shell was confirmed by measuring the rate of the formation of Fe-DES inside HoSF and an activation energy of 58.4 kJ/mol was determined. An attempt was made to determine the rate of iron (2+ and 3+) transit out from the ferritin interior by adding excess bipyridine or DES to PB trapped within the HoSF interior. However, the reactions are slow and occur at almost identical rates for free and HoSF-encapsulated PB, indicating that the transfer of iron from the interior through the

Synthesis, Characterization and Gas Sensing Properties of Ag@α-Fe2O3 Core–Shell Nanocomposites

Directory of Open Access Journals (Sweden)

Ali Mirzaei

2015-05-01

Full Text Available Ag@α-Fe2O3 nanocomposite having a core–shell structure was synthesized by a two-step reduction-sol gel approach, including Ag nanoparticles synthesis by sodium borohydride as the reducing agent in a first step and the subsequent mixing with a Fe+3 sol for α-Fe2O3 coating. The synthesized Ag@α-Fe2O3 nanocomposite has been characterized by various techniques, such as SEM, TEM and UV-Vis spectroscopy. The electrical and gas sensing properties of the synthesized composite towards low concentrations of ethanol have been evaluated. The Ag@α-Fe2O3 nanocomposite showed better sensing characteristics than the pure α-Fe2O3. The peculiar hierarchical nano-architecture and the chemical and electronic sensitization effect of Ag nanoparticles in Ag@α-Fe2O3 sensors were postulated to play a key role in modulating gas-sensing properties in comparison to pristine α-Fe2O3 sensors.

Nitrogen–doped graphitized carbon shell encapsulated NiFe nanoparticles: A highly durable oxygen evolution catalyst

Energy Technology Data Exchange (ETDEWEB)

Du, Lei; Luo, Langli; Feng, Zhenxing; Engelhard, Mark; Xie, Xiaohong; Han, Binghong; Sun, Junming; Zhang, Jianghao; Yin, Geping; Wang, Chongmin; Wang, Yong; Shao, Yuyan

2017-09-01

Oxygen evolution reaction (OER) plays a crucial role in various energy conversion devices such as water electrolyzers and metal–air batteries. Precious metal catalysts such as Ir, Ru and their oxides are usually used for enhanced reaction kinetics but are limited by their scarce resource. The challenges associated with alternative non–precious metal catalysts such as transition metal oxides and (oxy)hydroxides etc. are their low electronic conductivity and poor durability. Here, we report OER catalysts of NiFe nanoparticles encapsulated by nitrogen–doped graphitized carbon shells derived from bimetallic metal–organic frameworks (MOFs) precursors. The optimal OER catalyst shows excellent activity (360 mV overpotential at 10 mA cm–2GEO) and durability (no obvious degradation after 20 000 cycles). The electron-donation from Fe and tuned electronic structure of metal cores by Ni are revealed to be primary contributors to the enhanced OER activity. We further demonstrated that the structure and morphology of encapsulating carbon shells, which are the key factors influencing the durability, are facilely controlled by chemical state of precursors. Severe metal particle growth probably caused by oxidation of carbon shells and encapsulated nanoparticles is believed to the main mechanism for activity degradation in these catalysts.

Synthesis of Core/Shell MnFe2O4/Au Nanoparticles for Advanced Proton Treatment

International Nuclear Information System (INIS)

Park, Jeong Chan

2014-01-01

Among many approaches for the surface modification with materials, such as polymers, organic ligands and metals, one of the most attractive ways is using metals. The fabrication of metal-based, monolayer-coated magnetic nanoparticles has been intensively studied. However, the synthesis of metal-capped magnetic nanoparticles with monodIspersities and controllable sizes is still challenged. Recently, gold-capped magnetic nanoparticles have been reported to increase stability and to provide biocompatibility. Magnetic nanoparticle with gold coating is an attractive system, which can be stabilized in biological conditions and readily functionalized through well-established surface modification (Au-S) chemistry. The Au coating offers plasmonic properties to magnetic nanoparticles. The core/shell nanoparticles were transferred from organic to aqueous solutions for biomedical applications. The core/shell structured MnFe 2 O 4 /Au nanoparticles have been prepared and transferred from organic phase to aqueous solutions. The resulting Au-coated nanocrystals may be an attractive system for biomedical applications, which are needed both magnetic resonance imaging and optical imaging. The phase transferred core/shell nanoparticles can be decorated with targeting moiety, such as antibodies, peptides, aptamers, small molecules and ligands for biological applications. The proton treatment with the resulting Au-MnFe 2 O 4 nanoparticles is undergoing.

Fe-N co-doped SiO2@TiO2 yolk-shell hollow nanospheres with enhanced visible light photocatalytic degradation

Science.gov (United States)

Wan, Hengcheng; Yao, Weitang; Zhu, Wenkun; Tang, Yi; Ge, Huilin; Shi, Xiaozhong; Duan, Tao

2018-06-01

SiO2@TiO2 yolk@shell hollow nanospheres (STNSs) is considered as an outstanding photocatalyst due to its tunable structure and composition. Based on this point, we present an unprecedentedly excellent photocatalytic property of STNSs toward tannic acid via a Fe-N co-doped strategy. Their morphologies, compositions, structure and properties are characterized. The Fe-N co-doped STNSs formed good hollow yolk@shell structure. The results show that the energy gap of the composites can be downgraded to 2.82 eV (pure TiO2 = 3.2 eV). Photocatalytic degradation of tannic acid (TA, 30 mg L-1) under visible light (380 nm TiO2 nanospheres, non-doped STNSs and N-doped STNSs, the Fe-N co-doped STNSs exhibits the highest activity, which can degrade 99.5% TA into CO2 and H2O in 80 min. The probable degradation mechanism of the composites is simultaneously proposed, the band gap of STNSs becomes narrow by co-doping Fe-N, so that the TiO2 shell can stimulate electrons under visible light exposure, generate the ions of radOH and radO2- with a strong oxidizing property. Therefore this approach works is much desired for radioactive organic wastewater photocatalytic degradation.

Controllable Fabrication of Fe3O4/ZnO Core–Shell Nanocomposites and Their Electromagnetic Wave Absorption Performance in the 2–18 GHz Frequency Range

Directory of Open Access Journals (Sweden)

Xiaodong Sun

2018-05-01

Full Text Available In this study, Fe3O4/ZnO core–shell nanocomposites were synthesized through a chemical method of coating the magnetic core (Fe3O4 with ZnO by co-precipitation of Fe3O4 with zinc acetate in a basic medium of ammonium hydroxide. The phase structure, morphology and electromagnetic parameters of the Fe3O4/ZnO core–shell nanocomposites were investigated. The results indicated that the concentration of the solvent was responsible for controlling the morphology of the composites, which further influenced their impedance matching and microwave absorption properties. Moreover, Fe3O4/ZnO nanocomposites exhibited an enhanced absorption capacity in comparison with the naked Fe3O4 nanospheres. Specifically, the minimum reflection loss value reached −50.79 dB at 4.38 GHz when the thickness was 4.5 mm. It is expected that the Fe3O4/ZnO core–shell structured nanocomposites could be a promising candidate as high-performance microwave absorbers.

Magnetically separable core–shell ZnFe_2O_4@ZnO nanoparticles for visible light photodegradation of methyl orange

International Nuclear Information System (INIS)

Kulkarni, Suresh D.; Kumbar, Sagar; Menon, Samvit G.; Choudhari, K.S.; Santhosh, C.

2016-01-01

Highlights: • Phase pure, magnetic ZnFe_2O_4@ZnO nanoparticles synthesized with excellent yield. • ZnFe_2O_4@ZnO displayed higher UV photocatalytic efficiency than ZnO nanoparticles. • First report on visible light photodegradation of methyl orange by ZnFe_2O_4@ZnO. • Excellent reusability of ZnFe_2O_4@ZnO nanoparticles observed for azo dye removal. - Abstract: Visible light photodegradation of aqueous methyl orange using magnetically separable core–shell ZnFe_2O_4@ZnO nanoparticles is reported. A combination of low temperature (190 °C) microwave synthesis and hydrothermal method were used to prepare phase pure material with excellent yield (95%). The magnetic separability, surface area of 41 m"2/g and visible light absorption make ZnFe_2O_4@ZnO nanoparticles a good solar photocatalyst. ZnFe_2O_4@ZnO displayed greater UV photocatalytic efficiency than ZnO owing to the generation of large number of electron-hole pairs. Visible light photodegradation of MO using ZnFe_2O_4@ZnO nanoparticles is reported for the first time. Higher first order rate constants under both UV and visible light for core-shell nanoparticles suggested their superiority over its individual oxides. The ZnFe_2O_4@ZnO showed excellent reusability with high photocatalytic efficiencies suggesting its suitability for solar photocatalytic applications.

Microstructure, texture, and magnetic properties of backward extruded NdFeB ring magnets

International Nuclear Information System (INIS)

Gruenberger, W.; Hinz, D.; Schlaefer, D.; Schultz, L.

1996-01-01

Radially-oriented NdFeB ring magnets have been prepared by backward extrusion of melt-spun material. The average remanence measured in the radial direction reaches values above 1.2 T. Due to the inhomogeneity of the deformation, the magnetic properties and X-ray diffraction patterns revealed a gradual improvement of the alignment from the outer shell to regions near the inner surface of the ring. (orig.)

Radioactive 55Fe contamination in the primary circuit of WWER-440

International Nuclear Information System (INIS)

Ruskov, T.; Ruskov, R.; Dobrevski, I.; Konnova, S.; Zaharieva, N.; Menut, P.

2001-01-01

The isotope 55 Fe generation in the steel construction materials of the reactor and the mechanism of internal irradiation and blood affection by the 55 Fe are briefly discussed in this paper. The paper also presents the results from calculation of direct generation of 55 Fe due to neutron irradiation of different iron-contained parts of the reactor system such as the steel shell of the reactor core, the core basket, the steel shaft of the reactor vessels. Calculations are performed with specially developed program code DIRGEN. Another type of contamination, considered in the paper is due to the corrosion of materials and erosion-dissolution processes in the primary circuit of WWER with their subsequent deposition-precipitation on the inner surface of the primary circuit. The real time calculations of the 55 Fe activity are performed, by using of the updated computer code MIGA-RT. The obtained results show that the 55 Fe activity deposition on the inner surfaces of the primary circuits reaches the values of 103 kBq/cm 2 for the reactor core surfaces and 102 kBq/cm 2 for the out-of-core surfaces. The activity values are in one order of magnitude higher than the corresponding activity values due to 60 Co buildup

A novel platform of hemoglobin on core-shell structurally Fe{sub 3}O{sub 4}-Au nanoparticles and its direct electrochemistry

Energy Technology Data Exchange (ETDEWEB)

Liu Yang; Han Ting; Chen Chao; Bao Ning; Yu Chunmei [Institute of Analytical Chemistry for Life Science, School of Public Health, Nantong University, Nantong 226019 (China); Gu Haiying, E-mail: hygu@ntu.edu.c [Institute of Analytical Chemistry for Life Science, School of Public Health, Nantong University, Nantong 226019 (China)

2011-03-30

Research highlights: {yields} In recent years, immobilization of biomolecule onto nanomaterials, which could be utilized in the investigation of biomolecule reactions and the preparations of the biosensors, has attracted much research attention. A novel platform, which hemoglobin (Hb) was immobilized on core-shell structurally Fe{sub 3}O{sub 4}/Au nanoparticles (simplified as Fe{sub 3}O{sub 4}-Au NPs) modified glassy carbon electrode (GCE), has been developed for fabricating the third biosensors in this paper. {yields} Magnetic NPs stand out because of their added properties. However, naked Fe{sub 3}O{sub 4} NPs are very sensitive to oxidation because of their high chemical reactivity and being prone to aggregate. Those defects limit their further applications. We presented a simple approach to synthesize Au modified Fe{sub 3}O{sub 4} NPs with core-shell structure, which was characterized by transmission electron microscopy, scanning electron microscope, energy dispersive spectra and UV-vis spectroscopy. {yields} The thermodynamics, dynamics and catalysis properties of Hb immobilized on Fe{sub 3}O{sub 4}-Au NPs were discussed by UV-visible spectrum, electrochemical impedance spectroscopy, electrochemical quartz crystal microbalance technique and cyclic voltammetry. The electrocatalytic behaviors of the immobilized Hb on Fe{sub 3}O{sub 4}-Au NPs were applied for the determination of hydrogen peroxide, oxygen and trichloroacetic acid. The possible functions of Fe{sub 3}O{sub 4} core and Au shell as a novel platform for achieving Hb direct electrochemistry were also discussed, respectively. - Abstract: A novel platform, which hemoglobin (Hb) was immobilized on core-shell structurally Fe{sub 3}O{sub 4}/Au nanoparticles (simplified as Fe{sub 3}O{sub 4}-Au NPs) modified glassy carbon electrode (GCE), has been developed for fabricating the third biosensors. Fe{sub 3}O{sub 4}-Au NPs, characterized using transmission electron microscope (TEM), scanning electron microscope

Crossover from disordered to core-shell structures of nano-oxide Y{sub 2}O{sub 3} dispersed particles in Fe

Energy Technology Data Exchange (ETDEWEB)

Higgins, M. P.; Wang, L. M.; Gao, F., E-mail: gaofeium@umich.edu [Department of Nuclear Engineering and Radiological Sciences, University of Michigan, Ann Arbor, Michigan 48109 (United States); Lu, C. Y. [Department of Nuclear Engineering and Radiological Sciences, University of Michigan, Ann Arbor, Michigan 48109 (United States); Key Laboratory for Anisotropy and Texture of Materials (Ministry of Education), Northeastern University, Shenyang, Liaoning 110819 (China); Lu, Z. [Key Laboratory for Anisotropy and Texture of Materials (Ministry of Education), Northeastern University, Shenyang, Liaoning 110819 (China); Shao, L. [Department of Nuclear Engineering, Texas A& M University, College Station, Texas 77843 (United States)

2016-07-18

Molecular dynamic simulations of Y{sub 2}O{sub 3} in bcc Fe and transmission electron microscopy (TEM) observations were used to understand the structure of Y{sub 2}O{sub 3} nano-clusters in an oxide dispersion strengthened steel matrix. The study showed that Y{sub 2}O{sub 3} nano-clusters below 2 nm were completely disordered. Y{sub 2}O{sub 3} nano-clusters above 2 nm, however, form a core-shell structure, with a shell thickness of 0.5–0.7 nm that is independent of nano-cluster size. Y{sub 2}O{sub 3} nano-clusters were surrounded by off-lattice Fe atoms, further increasing the stability of these nano-clusters. TEM was used to corroborate our simulation results and showed a crossover from a disordered nano-cluster to a core-shell structure.

Synthesis and cytotoxicity study of magnesium ferrite-gold core-shell nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Nonkumwong, Jeeranan [Department of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Pakawanit, Phakkhananan [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Wipatanawin, Angkana [Division of Biochemistry and Biochemical Technology, Department of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Jantaratana, Pongsakorn [Department of Physics, Faculty of Science, Kasetsart University, Bangkok 11900 (Thailand); Ananta, Supon [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand); Srisombat, Laongnuan, E-mail: slaongnuan@yahoo.com [Department of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200 (Thailand)

2016-04-01

In this work, the core-magnesium ferrite (MgFe{sub 2}O{sub 4}) nanoparticles were prepared by hydrothermal technique. Completed gold (Au) shell coating on the surfaces of MgFe{sub 2}O{sub 4} nanoparticles was obtained by varying core/shell ratios via a reduction method. Phase identification, morphological evolution, optical properties, magnetic properties and cytotoxicity to mammalian cells of these MgFe{sub 2}O{sub 4} core coated with Au nanoparticles were examined by using a combination of X-ray diffraction, scanning electron microscopy, transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy, UV–visible spectroscopy (UV–vis), vibrating sample magnetometry and resazurin microplate assay techniques. In general, TEM images revealed different sizes of the core-shell nanoparticles generated from various core/shell ratios and confirmed the completed Au shell coating on MgFe{sub 2}O{sub 4} core nanoparticles via suitable core/shell ratio with particle size less than 100 nm. The core-shell nanoparticle size and the quality of coating influence the optical properties of the products. The UV–vis spectra of complete coated MgFe{sub 2}O{sub 4}-Au core-shell nanoparticles exhibit the absorption bands in the near-Infrared (NIR) region indicating high potential for therapeutic applications. Based on the magnetic property measurement, it was found that the obtained MgFe{sub 2}O{sub 4}-Au core-shell nanoparticles still exhibit superparamagnetism with lower saturation magnetization value, compared with MgFe{sub 2}O{sub 4} core. Both of MgFe{sub 2}O{sub 4} and MgFe{sub 2}O{sub 4}-Au core-shell also showed in vitro non-cytotoxicity to mouse areola fibroblast (L-929) cell line. - Highlights: • Synthesis of MgFe{sub 2}O{sub 4}-Au core-shell nanoparticles with particle size < 100 nm • Complete Au shell coating on the surfaces of MgFe{sub 2}O{sub 4} nanoparticles • In vitro cytotoxicity study of complete coated MgFe{sub 2}O{sub 4}-Au core-shell

Synthesis and cytotoxicity study of magnesium ferrite-gold core-shell nanoparticles

International Nuclear Information System (INIS)

Nonkumwong, Jeeranan; Pakawanit, Phakkhananan; Wipatanawin, Angkana; Jantaratana, Pongsakorn; Ananta, Supon; Srisombat, Laongnuan

2016-01-01

In this work, the core-magnesium ferrite (MgFe_2O_4) nanoparticles were prepared by hydrothermal technique. Completed gold (Au) shell coating on the surfaces of MgFe_2O_4 nanoparticles was obtained by varying core/shell ratios via a reduction method. Phase identification, morphological evolution, optical properties, magnetic properties and cytotoxicity to mammalian cells of these MgFe_2O_4 core coated with Au nanoparticles were examined by using a combination of X-ray diffraction, scanning electron microscopy, transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy, UV–visible spectroscopy (UV–vis), vibrating sample magnetometry and resazurin microplate assay techniques. In general, TEM images revealed different sizes of the core-shell nanoparticles generated from various core/shell ratios and confirmed the completed Au shell coating on MgFe_2O_4 core nanoparticles via suitable core/shell ratio with particle size less than 100 nm. The core-shell nanoparticle size and the quality of coating influence the optical properties of the products. The UV–vis spectra of complete coated MgFe_2O_4-Au core-shell nanoparticles exhibit the absorption bands in the near-Infrared (NIR) region indicating high potential for therapeutic applications. Based on the magnetic property measurement, it was found that the obtained MgFe_2O_4-Au core-shell nanoparticles still exhibit superparamagnetism with lower saturation magnetization value, compared with MgFe_2O_4 core. Both of MgFe_2O_4 and MgFe_2O_4-Au core-shell also showed in vitro non-cytotoxicity to mouse areola fibroblast (L-929) cell line. - Highlights: • Synthesis of MgFe_2O_4-Au core-shell nanoparticles with particle size < 100 nm • Complete Au shell coating on the surfaces of MgFe_2O_4 nanoparticles • In vitro cytotoxicity study of complete coated MgFe_2O_4-Au core-shell nanoparticles

Enhanced rate capability and cycling stability of core/shell structured CoFe{sub 2}O{sub 4}/onion-like C nanocapsules for lithium-ion battery anodes

Energy Technology Data Exchange (ETDEWEB)

Liu, Xianguo, E-mail: liuxianguohugh@gmail.com [School of Materials Science and Engineering, Anhui University of Technology, Maanshan 243002 (China); Wu, Niandu; Cui, Caiyun; Zhou, Pingping [School of Materials Science and Engineering, Anhui University of Technology, Maanshan 243002 (China); Sun, Yuping [Center for Engineering Practice and Innovation Education, Anhui University of Technology, Maanshan 243032 (China)

2015-09-25

Highlights: • Core/shell-structured CoFe{sub 2}O{sub 4}/onion-like carbon nanocapsules have been prepared. • CoFe{sub 2}O{sub 4}/C nanocapsules possess good reversibility even when the current density is up to 4C. • CoFe{sub 2}O{sub 4}/C nanocapsules obtain a discharge capacity of 914.2 mA h g{sup −1} after 500 cycles at 0.1C. - Abstract: In this work, core/shell structured CoFe{sub 2}O{sub 4}/onion-like C nanocapsules have been successfully fabricated by the arc discharge method and air-annealing process and confirmed by X-ray diffraction and high-resolution transmission electron microscopy. The core/shell structure effectively withstands the volume change of CoFe{sub 2}O{sub 4} nanoparticles during the cycling process. Moreover, the onion-like C shells reduce the charge transfer resistance and facilitate electron and ion transport throughout the electrode. As a result, CoFe{sub 2}O{sub 4}/onion-like C nanocapsules exhibit excellent performance as a potential anode material for lithium ion batteries and deliver a reversible capacity of 914.2 mA h g{sup −1} at 0.1C, even after 500 cycles and recover its original capacity when the rate returns from 4C to the initial 0.1C after 120 cycles.

Core-shelled mesoporous CoFe2O4-SiO2 material with good adsorption and high-temperature magnetic recycling capabilities

Science.gov (United States)

Li, Zhi'ang; Wang, Jianlin; Liu, Min; Chen, Tong; Chen, Jifang; Ge, Wen; Fu, Zhengping; Peng, Ranran; Zhai, Xiaofang; Lu, Yalin

2018-04-01

Residues of organic dye in industrial effluents cause severe water system pollution. Although several methods, such as biodegradation and activated carbon adsorption, are available for treating these effluents before their discharge into waterbodies, secondary pollution by adsorbents and degrading products remains an issue. Therefore, new materials should be identified to solve this problem. In this work, CoFe2O4-SiO2 core-shell structures were synthesized using an improved Stöber method by coating mesoporous silica onto CoFe2O4 nanoparticles. The specific surface areas of the synthesized particles range from 30 m2/g to 150 m2/g and vary according to the dosage amount of tetraethoxysilane. Such core-shelled nanoparticles have the following advantages for treating industrial effluents mixed with dye: good adsorption capability, above-room-temperature magnetic recycling capability, and heat-enduring stability. Through adsorption of methylene blue, a typical dyeing material, the core-shell-structured particles show a good adsorption capability of approximately 33 mg/L. The particles are easily and completely collected by magnets, which is possible due to the magnetic property of core CoFe2O4. Heat treatment can burn out the adsorbed dyes and good adsorption performance is sustained even after several heat-treating loops. This property overcomes the common problem of particles with Fe3O4 as a core, by which Fe3O4 is oxidized to nonmagnetic α-Fe2O3 at the burning temperature. We also designed a miniature of effluent-treating pipeline, which demonstrates the potential of the application.

Double containment shell for nuclear power plants

International Nuclear Information System (INIS)

Sykora, D.

1977-01-01

A double containment shell is proposed for nuclear power plants, especially those equipped with pressurized water reactors. The shell offers increased environmental protection from primary circuit accidents. The inner shell is built of steel or concrete while the outer shell is always built of concrete. The space between the two shells is filled with water and is provided with several manholes and with stiffeners designed for compensation for load due to the water hydrostatic pressure. Water serves the airtight separation of the containment shell inside from the environment and the absorption of heat released in a primary circuit accident. In case the inner shell is made of concrete, it is provided with heat-removal tubes in-built in its walls ensuring rapid heat transfer from the inside of the containment to the water in the interwall space. (Z.M.)

An image quality comparison study between XVI and OBI CBCT systems.

Science.gov (United States)

Kamath, Srijit; Song, William; Chvetsov, Alexei; Ozawa, Shuichi; Lu, Haibin; Samant, Sanjiv; Liu, Chihray; Li, Jonathan G; Palta, Jatinder R

2011-02-04

The purpose of this study is to evaluate and compare image quality characteristics for two commonly used and commercially available CBCT systems: the X-ray Volumetric Imager and the On-Board Imager. A commonly used CATPHAN image quality phantom was used to measure various image quality parameters, namely, pixel value stability and accuracy, noise, contrast to noise ratio (CNR), high-contrast resolution, low contrast resolution and image uniformity. For the XVI unit, we evaluated the image quality for four manufacturer-supplied protocols as a function of mAs. For the OBI unit, we did the same for the full-fan and half-fan scanning modes, which were respectively used with the full bow-tie and half bow-tie filters. For XVI, the mean pixel values of regions of interest were found to generally decrease with increasing mAs for all protocols, while they were relatively stable with mAs for OBI. Noise was slightly lower on XVI and was seen to decrease with increasing mAs, while CNR increased with mAs for both systems. For XVI and OBI, the high-contrast resolution was approximately limited by the pixel resolution of the reconstructed image. On OBI images, up to 6 and 5 discs of 1% and 0.5% contrast, respectively, were visible for a high mAs setting using the full-fan mode, while none of the discs were clearly visible on the XVI images for various mAs settings when the medium resolution reconstruction was used. In conclusion, image quality parameters for XVI and OBI have been quantified and compared for clinical protocols under various mAs settings. These results need to be viewed in the context of a recent study that reported the dose-mAs relationship for the two systems and found that OBI generally delivered higher imaging doses than XVI.

Ionization of inner shells of atoms taking account of outer shell rearrangement

International Nuclear Information System (INIS)

Amusia, M.Ya.

1977-01-01

The application of the general many-body theory and methods formulated with its help, in particular, the so-called random phase approximation with exchange (RPAE) and the many-body perturbation theory (MBPT) makes possible a description of ionization processes for many outer and intermediate shells of a number of atoms. This investigation of outer- and intermediate-shell ionization by photons and electrons demonstrates the collective character of these processes and the possibility of describing them by RPAE. 28 references

Nitrogen–doped graphitized carbon shell encapsulated NiFe nanoparticles: A highly durable oxygen evolution catalyst

Energy Technology Data Exchange (ETDEWEB)

Du, Lei; Luo, Langli; Feng, Zhenxing; Engelhard, Mark; Xie, Xiaohong; Han, Binghong; Sun, Junming; Zhang, Jianghao; Yin, Geping; Wang, Chongmin; Wang, Yong; Shao, Yuyan

2017-09-01

Oxygen evolution reaction (OER) plays a crucial role in various energy conversion devices such as water electrolyzers and metal–air batteries. Precious metal catalysts such as Ir, Ru and their oxides are usually used for enhancing reaction kinetics but are limited by their scarce resource. The challenges associated with alternative non–precious metal catalysts such as transition metal oxides and (oxy)hydroxides etc. are their low electronic conductivity and durability. Herein, we report a highly active (360 mV overpotential at 10 mA cm–2GEO) and durable (no degradation after 20000 cycles) OER catalyst derived from bimetallic metal–organic frameworks (MOFs) precursors. This catalyst consists of NiFe nanoparticles encapsulated by nitrogen–doped graphitized carbon shells. The electron-donation/deviation from Fe and tuned electronic structure of metal cores by Ni are revealed to be primary contributors to the enhanced OER activity, whereas N concentration contributes negligibly. We further demonstrated that the structure and morphology of encapsulating carbon shells, which are the key factors influencing the durability, are facilely controlled by the chemical state of precursors.

Accurate Wavelength Measurements and Modeling of Fe XV to Fe XIX Spectra Recorded in High-Density Plasmas between 13.5 and 17 Å

Science.gov (United States)

May, M. J.; Beiersdorfer, P.; Dunn, J.; Jordan, N.; Hansen, S. B.; Osterheld, A. L.; Faenov, A. Ya.; Pikuz, T. A.; Skobelev, I. Yu.; Flora, F.; Bollanti, S.; Di Lazzaro, P.; Murra, D.; Reale, A.; Reale, L.; Tomassetti, G.; Ritucci, A.; Francucci, M.; Martellucci, S.; Petrocelli, G.

2005-06-01

Iron spectra have been recorded from plasmas created at three different laser plasma facilities: the Tor Vergata University laser in Rome (Italy), the Hercules laser at ENEA in Frascati (Italy), and the Compact Multipulse Terawatt (COMET) laser at LLNL in California (USA). The measurements provide a means of identifying dielectronic satellite lines from Fe XVI and Fe XV in the vicinity of the strong 2p-->3d transitions of Fe XVII. About 80 Δn>=1 lines of Fe XV (Mg-like) to Fe XIX (O-like) were recorded between 13.8 and 17.1 Å with a high spectral resolution (λ/Δλ~4000) about 30 of these lines are from Fe XVI and Fe XV. The laser-produced plasmas had electron temperatures between 100 and 500 eV and electron densities between 1020 and 1022 cm-3. The Hebrew University Lawrence Livermore Atomic Code (HULLAC) was used to calculate the atomic structure and atomic rates for Fe XV-XIX. HULLAC was used to calculate synthetic line intensities at Te=200 eV and ne=1021 cm-3 for three different conditions to illustrate the role of opacity: optically thin plasmas with no excitation-autoionization/dielectronic recombination (EA/DR) contributions to the line intensities, optically thin plasmas that included EA/DR contributions to the line intensities, and optically thick plasmas (optical depth ~200 μm) that included EA/DR contributions to the line intensities. The optically thick simulation best reproduced the recorded spectrum from the Hercules laser. However, some discrepancies between the modeling and the recorded spectra remain.

Synthesis of triaxial LiFePO4 nanowire with a VGCF core column and a carbon shell through the electrospinning method.

Science.gov (United States)

Hosono, Eiji; Wang, Yonggang; Kida, Noriyuki; Enomoto, Masaya; Kojima, Norimichi; Okubo, Masashi; Matsuda, Hirofumi; Saito, Yoshiyasu; Kudo, Tetsuichi; Honma, Itaru; Zhou, Haoshen

2010-01-01

A triaxial LiFePO4 nanowire with a multi wall carbon nanotube (VGCF:Vapor-grown carbon fiber) core column and an outer shell of amorphous carbon was successfully synthesized through the electrospinning method. The carbon nanotube core oriented in the direction of the wire played an important role in the conduction of electrons during the charge-discharge process, whereas the outer amorphous carbon shell suppressed the oxidation of Fe2+. An electrode with uniformly dispersed carbon and active materials was easily fabricated via a single process by heating after the electrospinning method is applied. Mossbauer spectroscopy for the nanowire showed a broadening of the line width, indicating a disordered coordination environment of the Fe ion near the surface. The electrospinning method was proven to be suitable for the fabrication of a triaxial nanostructure.

Synthesis of green Fe3+/glucose/rGO electrode for supercapacitor application assisted by chemical exfoliation process from burning coconut shell

Science.gov (United States)

Putra, Gilang B. A.; Pradana, Herdy Y.; Soenaryo, Dimas E. T.; Baqiya, Malik A.; Darminto

2018-04-01

For the goal of large, environmental - friendly, renewable, and inexpensive energy storage, the development of supercapacitor electrodes is needed, by anchoring transition metal oxide (Fe3+ ion) as pseudo capacitor electrode material with reduced graphene oxide (rGO) from an old coconut shell as electrochemical double layer capacitor (EDLC). This porous electrode composite is prepared by sonication and chemical exfoliation assisted by acid. Synthesis of supercapacitor is also added by glucose, which acts as a spacer between layers of rGO to increase the capacitance, also as binder between the materials used. Combining Fe3+ with old coconut shell rGO give high specific capacitance of up to 99 F/g at a potential window of -1 V to 1 V. The Fe3+/glucose/rGO electrode has thickness of up to 57 nm (from PSA result) and give a uniform distribution from EDX mapping with disperse Fe domains and not bonding with rGO.

Folic acid-functionalized magnetic ZnFe2O4 hollow microsphere core/mesoporous silica shell composite particles: synthesis and application in drug release.

Science.gov (United States)

Yang, Dandan; Wei, Kaiwei; Liu, Qi; Yang, Yong; Guo, Xue; Rong, Hongren; Cheng, Mei-Ling; Wang, Guoxiu

2013-07-01

A drug delivery system was designed by deliberately combining the useful functions into one entity, which was composed of magnetic ZnFe2O4 hollow microsphere as the core, and mesoporous silica with folic acid molecules as the outer shell. Amine groups coated magnetic ZnFe2O4 hollow microsphere core/mesoporous silica shell (MZHM-MSS-NH2) composite particles were first synthesized by a one-pot direct co-condensation method. Subsequently a novel kind of folic acid-functionalized magnetic ZnFe2O4 hollow microsphere core/mesoporous silica shell (MZHM-MSS-NHFA) composite particles were synthesized by conjugating folic acid as targeted molecule to MZHM-MSS-NH2. Ibuprofen, a well-known antiphlogistic drug, was used as a model drug to assess the loading and releasing behavior of the composite microspheres. The results show that the MZHM-MSS-NHFA system has the higher capacity of drug storage and good sustained drug-release property. Copyright © 2013 Elsevier B.V. All rights reserved.

Design of epoxy-functionalized Fe3O4@MCM-41 core-shell nanoparticles for enzyme immobilization.

Science.gov (United States)

Ulu, Ahmet; Ozcan, Imren; Koytepe, Suleyman; Ates, Burhan

2018-05-01

The scope of our research was to prepare the organosilane-modified Fe 3 O 4 @MCM-41 core-shell magnetic nanoparticles, used for L-ASNase immobilization and explored screening of immobilization conditions such as pH, temperature, thermal stability, kinetic parameters, reusability and storage stability. In this content, Fe 3 O 4 core-shell magnetic nanoparticles were prepared via co-precipitation method and coated with MCM-41. Then, Fe 3 O 4 @MCM-41 magnetic nanoparticles were functionalized by (3-glycidyloxypropyl) trimethoxysilane (GPTMS) as an organosilane compound. Subsequently, L-ASNase was covalently immobilized on epoxy-functionalized Fe 3 O 4 @MCM-41 magnetic nanoparticles. The immobilized L-ASNase had greater activity at high pH and temperature values. It also maintained >92% of the initial activity after incubation at 55 °C for 3 h. Regarding kinetic values, immobilized L-ASNase showed a higher Vmax and lower Km compared to native L-ASNase. In addition, it displayed excellent reusability for 12 successive cycles. After 30 days of storage at 4 °C and 25 °C, immobilized L-ASNase retained 54% and 26% of its initial activities while native L-ASNase lost about 68% and 84% of its initial activity, respectively. As a result, the immobilization of L-ASNase onto magnetic nanoparticles may provide an advantage in terms of removal of L-ASNase from reaction media. Copyright © 2018. Published by Elsevier B.V.

Aqueous-phase synthesis and color-tuning of core/shell/shell inorganic nanocrystals consisting of ZnSe, (Cu, Mn)-doped ZnS, and ZnS

Energy Technology Data Exchange (ETDEWEB)

Choi, Jongwan; Yoon, Sujin [Department of Chemistry and Research Institute for Natural Science, Hanyang University, Seoul, 133-791 (Korea, Republic of); Kim, Felix Sunjoo, E-mail: fskim@cau.ac.kr [School of Chemical Engineering and Materials Science, Chung-Ang University, Seoul, 156-756 (Korea, Republic of); Kim, Nakjoong, E-mail: kimnj@hanyang.ac.kr [Department of Chemistry and Research Institute for Natural Science, Hanyang University, Seoul, 133-791 (Korea, Republic of)

2016-06-25

We report synthesis of colloidal nanocrystals based on ZnSe core, (Cu,Mn)-doped ZnS inner-shell, and ZnS outer-shell by using an eco-friendly method and their optical properties. Synthesis of core/shell/shell nanocrystals was performed by using a one-pot/three-step colloidal method with 3-mercaptopropionic acid as a stabilizer in aqueous phase at low temperature. A double-shell structure was employed with inner-shell as a host for doping and outer-shell as a passivation layer for covering surface defects. Copper and manganese were introduced as single- or co-dopants during inner-shell formation, providing an effective means to control the emission color of the nanocrystals. The synthesized nanocrystals showed fluorescent emission ranging from blue to green, to white, and to orange, adjusted by doping components, amounts, and ratios. The photoluminescence quantum yields of the core/doped-shell/shell nanocrystals approached 36%. - Highlights: • ZnSe/ZnS:(Cu,Ms)/ZnS core/(doped)shell/shell nanocrystals were synthesized in an aqueous phase. • Emission color of nanocrystals was controlled from blue to white to orange by adjusting the atomic ratio of Cu and Mn co-dopants. • Photoluminescence quantum yields of the colloidal nanocrystals approached 36%.

Super-paramagnetic core-shell material with tunable magnetic behavior by regulating electron transfer efficiency and structure stability of the shell

Directory of Open Access Journals (Sweden)

Wenyan Zhang

Full Text Available In this work, a spherical nano core-shell material was constructed by encapsulating Fe3O4 microsphere into conductive polymer-metal composite shell. The Fe3O4 microspheres were fabricated by assembling large amounts of Fe3O4 nano-crystals, which endowed the microspheres with super-paramagnetic property and high saturation magnetization. The polymer-metal composite shell was constructed by inserting Pt nano-particles (NPs into the conductive polymer polypyrrole (PPy. As size and dispersion of the Pt NPs has an important influence on their surface area and surface energy, it was effective to enlarge the interface area between PPy and Pt NPs, enhance the electron transfer efficiency of PPy/Pt composite shell, and reinforced the shell’s structural stability just by tuning the size and dispersion of Pt NPs. Moreover, core-shell structure of the materials made it convenient to investigate the PPy/Pt shell’s shielding effect on the Fe3O4 core’s magnetic response to external magnetic fields. It was found that the saturation magnetization of Fe3O4/PPy/Pt core-shell material could be reduced by 20.5% by regulating the conductivity of the PPy/Pt shell. Keywords: Super-paramagnetic, Conductivity, Magnetic shielding, Structural stability

Fluoride adsorption from aqueous solution by magnetic core-shell Fe_3O_4@alginate-La particles fabricated via electro-coextrusion

International Nuclear Information System (INIS)

Zhang, Yahui; Lin, Xiaoyan; Zhou, Quisheng; Luo, Xuegang

2016-01-01

Graphical abstract: The magnetic core-shell Fe_3O_4@Alg-La particles were fabricated successfully by a simple method of electro-coextrusion, and employed as an adsorbent for separation of fluoride from aqueous solution. - Highlights: • Magnetic core-shell Fe_3O_4@Alg-La particles were prepared by electro-coextrusion. • The maximum adsorption capacity for fluoride at 298.15 K was 45.230 mg/g. • The adsorbent has a good saturation magnetization value. • The adsorbent has a great potential in removing the fluoride. - Abstract: The magnetic core-shell Fe_3O_4@Alg-La particles were fabricated successfully by a simple method of electro-coextrusion, and employed as an adsorbent for separation of fluoride from aqueous solution. Main factors affecting the removal of fluoride, including pH, adsorbent dosage, initial concentration, temperature and contact time were investigated. The adsorption isotherm and adsorption kinetics were studied to understand the adsorption process in detail. The experimental data were fitted well by the non-linear Freundlich isotherm and linear pseudo-second-order model, the maximum fluoride adsorption capacity was 45.230 mg/g at pH 4, 298.15 K. Thermodynamic parameters indicated that the fluoride adsorption process was feasible and spontaneous. The presence of other anions like Cl"−, SO_4"2"−, HCO_3"− and PO_4"3"− had almost no effect on the fluoride adsorption. The adsorbent can be easily separated from the solution by a magnet. The magnetic core-shell Fe_3O_4@Alg-La particles before and after fluoride adsorption were studied by SEM, FTIR, EDX and XPS, which indicated that the adsorption mechanism may be related to electrostatic attraction and Lewis acid-base interaction.

Transient-field strength measurements for 52Cr traversing Fe hosts at high velocity and polarization transfer mechanisms

International Nuclear Information System (INIS)

Stuchbery, A.E.; Doran, C.E.; Byrne, A.P.; Bolotin, H.H.; Dracoulis, G.D.

1986-12-01

Transient-field strengths were measured for 52 Cr ions traversing polarized Fe hosts at velocities up to 12v>=o (v>=o = c/137 = Bohr velocity). The results are compared with predictions of various transient field parametrizations and discussed in terms of possible mechanisms by which polarization might be transferred from the Fe host to inner vacancies of the moving Cr ions. The g-factor of the first 2 + state of 52 Cr was also measured by the transient field technique and found to be in accord with shell-model calculations

The inner mantle of the giant clam, Tridacna squamosa, expresses a basolateral Na+/K+-ATPase α-subunit, which displays light-dependent gene and protein expression along the shell-facing epithelium.

Directory of Open Access Journals (Sweden)

Mel V Boo

Full Text Available Na+/K+-ATPase (NKA is essential for maintaining the Na+ and K+ gradients, and supporting the secondary active transport of certain ions/molecules, across the plasma membrane of animal cells. This study aimed to clone the NKA α-subunit (NKAα from the inner mantle adjacent to the extrapallial fluid of Tridacna squamosa, to determine its subcellular localization, and to examine the effects of light exposure on its transcript level and protein abundance. The cDNA coding sequence of NKAα from T. squamosa comprised 3105 bp, encoding 1034 amino acids with an estimated molecular mass of 114 kDa. NKAα had a basolateral localization along the shell-facing epithelium of the inner mantle. Exposure to 12 h of light led to a significantly stronger basolateral NKAα-immunofluorescence at the shell-facing epithelium, indicating that NKA might play a role in light-enhanced calcification in T. squamosa. After 3 h of light exposure, the transcript level of NKAα decreased transiently in the inner mantle, but returned to the control level thereafter. In comparison, the protein abundance of NKAα remained unchanged at hour 3, but became significantly higher than the control after 12 h of light exposure. Hence, the expression of NKAα in the inner mantle of T. squamosa was light-dependent. It is probable that a higher expression level of NKA was needed in the shell-facing epithelial cells of the inner mantle to cope with a rise in Na+ influx, possibly caused by increases in activities of some Na+-dependent ion transporters/channels involved in light-enhanced calcification.

Retrieving transient conformational molecular structure information from inner-shell photoionization of laser-aligned molecules

Science.gov (United States)

Wang, Xu; Le, Anh-Thu; Yu, Chao; Lucchese, R. R.; Lin, C. D.

2016-01-01

We discuss a scheme to retrieve transient conformational molecular structure information using photoelectron angular distributions (PADs) that have averaged over partial alignments of isolated molecules. The photoelectron is pulled out from a localized inner-shell molecular orbital by an X-ray photon. We show that a transient change in the atomic positions from their equilibrium will lead to a sensitive change in the alignment-averaged PADs, which can be measured and used to retrieve the former. Exploiting the experimental convenience of changing the photon polarization direction, we show that it is advantageous to use PADs obtained from multiple photon polarization directions. A simple single-scattering model is proposed and benchmarked to describe the photoionization process and to do the retrieval using a multiple-parameter fitting method. PMID:27025410

Inelastic resonant M-scattering of X-rays from Gd metal with inner-shell excitation

International Nuclear Information System (INIS)

Braicovich, L.; Tagliaferri, A.

1998-01-01

The paper presents results on resonant inner-shell scattering in Gd across the M 5 threshold; the scattering channel with formally a 4 p hole in the final state is studied. Two scattering channels are in competition: one at constant transferred energy and another at constant outgoing energy. The branching ratio of the process at constant transferred energy is about 5%. It's isolated the many-body satellite structure of the formally 4p 3/2 final hole state and it's discussed the importance of the multiplet splitting and of the super Coster-Kronig conversion of this state into another final state with two 4 d holes. The results with resonant M 5 excitation are also compared with those of non-resonant excitation well above the M 4 threshold. Guidelines for future research are briefly presented

Fast electrons from multi-electron dynamics in xenon clusters induced by inner-shell ionization

International Nuclear Information System (INIS)

Bostedt, Christoph; Thomas, Heiko; Hoener, Matthias; Moeller, Thomas; Saalmann, Ulf; Georgescu, Ionut; Gnodtke, Christian; Rost, Jan-Michael

2010-01-01

Fast electrons emitted from xenon clusters in strong femtosecond 90 eV pulses have been measured at the Free-electron Laser in Hamburg (FLASH). Energy absorption occurs mainly through atomic inner-shell photo-ionization. Photo-electrons are trapped in the strong Coulomb potential of the cluster ions and form a non-equilibrium plasma with supra-atomic density. Its equilibration through multiple energy-exchanging collisions within the entire cluster volume produces electrons with energies well beyond the dominant emission line of atomic xenon. Here, in contrast to traditional low-frequency laser plasma heating, the plasma gains energy from electrons delivered through massive single-photon excitation from bound states. Electron emission induced by thermalization of a non-equilibrium plasma is expected to be a general phenomenon occurring for strong atomic x-ray absorption in extended systems.

Hi shells, supershells, shell-like objects, and ''worms''

International Nuclear Information System (INIS)

Heiles, C.

1984-01-01

We present photographic representations of the combination of two Hi surveys, so as to eliminate the survey boundaries at Vertical BarbVertical Bar = 10 0 . We also present high-contrast photographs for particular velocities to exhibit weak Hi features. All of these photographs were used to prepare a new list of Hi shells, supershells, and shell-like objects. We discuss the structure of three shell-like objects that are associated with high-velocity gas, and with gas at all velocities that is associated with radio continuum loops I, II, and III. We use spatial filtering to find wiggly gas filaments: ''worms'': crawling away from the galactic plane in the inner Galaxy. The ''worms'' are probably parts of shells that are open at the top; such shells should be good sources of hot gas for the galactic halo

Core–shell structure carbon coated ferric oxide (Fe{sub 2}O{sub 3}@C) nanoparticles for supercapacitors with superior electrochemical performance

Energy Technology Data Exchange (ETDEWEB)

Ye, Yipeng [School of Materials and Energy, Guangdong University of Technology, Guangzhou 510006 (China); Zhang, Haiyan [School of Materials and Energy, Guangdong University of Technology, Guangzhou 510006 (China); Guangdong Provincial Key Laboratory of Functional Soft Condensed Matter, Guangzhou 510006 (China); Chen, Yiming, E-mail: chenym@gdut.edu.cn [School of Materials and Energy, Guangdong University of Technology, Guangzhou 510006 (China); Guangdong Provincial Key Laboratory of Functional Soft Condensed Matter, Guangzhou 510006 (China); Deng, Peng; Huang, Zhikun [School of Materials and Energy, Guangdong University of Technology, Guangzhou 510006 (China); Liu, Liying; Qian, Yannan; Li, Yunyong [School of Materials and Energy, Guangdong University of Technology, Guangzhou 510006 (China); Guangdong Provincial Key Laboratory of Functional Soft Condensed Matter, Guangzhou 510006 (China); Li, Qingyu [School of Chemistry and Chemistry Engineering, Guangxi Normal University, Guilin 541004 (China)

2015-08-05

Highlights: • Fe{sub 2}O{sub 3}@C was prepared by using arc discharge method followed by heat treatment. • KOH activation made the core–shell structure Fe{sub 2}O{sub 3}@C porous. • The activated-Fe{sub 2}O{sub 3}@C supercapacitor exhibited superior electrochemical performance. - Abstract: Core–shell structure carbon coated ferric oxide nanoparticles (Fe{sub 2}O{sub 3}@C) were fabricated by the oxidation of carbon coated iron nanoparticles (Fe@C) prepared by a direct current carbon arc discharge method. Porous activated-Fe{sub 2}O{sub 3}@C was prepared by KOH activation of Fe{sub 2}O{sub 3}@C at the temperature of 750 °C. X-ray diffraction analysis (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were employed to characterize the structure and morphology of the Fe{sub 2}O{sub 3}@C and activated-Fe{sub 2}O{sub 3}@C. The specific surface area and pore size distribution of the samples were also tested. The activated-Fe{sub 2}O{sub 3}@C electrodes exhibited good electrochemical performance with a maximum specific capacitance of 612 F g{sup −1} at the charge/discharge current density of 0.5 A g{sup −1} with 5 M NaOH electrolyte. After 10,000 cycling DC tests at the charge/discharge current density of 4 A g{sup −1}, a high level specific capacitance of 518 F g{sup −1} was obtained (90.6% retention of the initial capacity), suggesting excellent long-term cycling stability.

High saturation magnetization FeB(C) nanocapsules

International Nuclear Information System (INIS)

Ma, S.; Si, P.Z.; Zhang, Y.; Wu, B.; Li, Y.B.; Liu, J.J.; Feng, W.J.; Ma, X.L.; Zhang, Z.D.

2007-01-01

FeB(C) nanocapsules were prepared by arc-discharging Fe 80 B 20 alloy in Ar and CH 4 . X-ray diffraction and transmission electron microscopy analyses showed that the FeB(C) nanocapsules had a core-shell structure with α-Fe and Fe 3 B as cores and graphite as shells. The formation mechanism of the FeB(C) nanocapsules is discussed. The graphite shells display a strong anti-acid effect. The saturation magnetization at room temperature of the FeB(C) nanocapsules is much higher than that of Fe(B) nanocapsules. The blocking temperature of FeB(C) nanocapsules is above 300 K

Inner-shell near-threshold photoionization of A-C60 endohedral atoms

International Nuclear Information System (INIS)

Baltenkov, Arkadiy S.; Dolmatov, Valery K.; Manson, Steven T.

2002-01-01

Photoelectron angular distributions and total photoionization cross sections of near-threshold 1s photoionization of Li from the oriented-in-space endohedral Li-C 60 fullerene are investigated within the framework of our recently developed photoionization theory of multicenter formations. Both at-the-center and off-the-center endohedral Li are considered, and off-the-center effects are shown to be of extreme importance, in contrast to the conventional wisdom. Multiple-scattering effects on the outgoing photoelectron are included and found to influence the photoionization spectra strongly, e.g., decreasing the cross section by more than an order of magnitude in certain cases, as compared to the situation when such effects are neglected. Diffraction resonances in the photoionization cross section of the endohedral Li atom are found as a result of the multicenter nature of the C 60 surrounding cage, and these are compared with the results of other empirical and ab initio theories. Since there is nothing particularly special about Li 1s with respect to photoionization, the trends uncovered in this paper should qualitatively apply to near-threshold inner-shell ns photoionization spectra of virtually any endohedral atom A from any A-C 60 endohedral fullerene formation

PBFA II lithium beam characterization from inner-shell x-ray images

International Nuclear Information System (INIS)

Moats, A.R.; Derzon, M.S.; Chandler, G.A.; Dukart, R.J.; Haill, T.A.

1994-01-01

The Particle Beam Fusion Accelerator (PBFA II) is not driving targets with ICF-relevant lithium ion beams. During the most recent lithium beam target series, time-integrated x-ray pinhole cameras viewed the ion-induced inner-shell x-ray fluorescence from the central gold cone target and a titanium-coated strip. Ion beam profiles at a nominal 10 mm radius and fixed azimuthal direction were obtained from images of the Ti K α , fluorescence of a Ti-coated Al diagnostic wire. The gold cone gave us beam profiles at a nominal 3 mm radius and at all azimuthal angles from the Au L α fluorescence. From these profiles, we obtained the ion beam vertical focus position, full-width-at-half-maximum, and the degree of azimuthal uniformity for the lithium target shots. For these initial results, beam steering problems were evident. Azimuthal uniformity was measured from the ion beam footprint on the outer Au case (predominantly Au L α ) of the hohlraum target and were found to be in the same range (up to 30%) as for previous proton beam target series. We then present plans for Li beam diagnostics for an upcoming target experimental series

Exchange-coupled Fe3O4/CoFe2O4 nanoparticles for advanced magnetic hyperthermia

Science.gov (United States)

Glassell, M.; Robles, J.; Das, R.; Phan, M. H.; Srikanth, H.

Iron oxide nanoparticles especially Fe3O4, γ-Fe2O3 have been extensively studied for magnetic hyperthermia because of their tunable magnetic properties and stable suspension in superparamagnetic regime. However, their relatively low heating capacity hindered practical application. Recently, a large improvement in heating efficiency has been reported in exchange-coupled nanoparticles with exchange coupling between soft and hard magnetic phases. Here, we systematically studied the effect of core and shell size on the heating efficiency of the Fe3O4/CoFe2O4 core/shell nanoparticles. The nanoparticles were synthesized using thermal decomposition of organometallic precursors. Transmission electron microscopy (TEM) showed formation of spherical shaped Fe3O4 and Fe3O-/CoFe2O4 nanoparticles. Magnetic measurements showed high magnetization (≅70 emu/g) and superparamagnetic behavior for the nanoparticles at room temperature. Magnetic hyperthermia results showed a large increase in specific absorption rate (SAR) for 8nm Fe3O4/CoFe2O4 compared to Fe3O4 nanoparticles of the same size. The heating efficiency of the Fe3O4/CoFe2O4 with 1 nm CoFe2O4 (shell) increased from 207 to 220 W/g (for 800 Oe) with increase in core size from 6 to 8 nm. The heating efficiency of the Fe3O4/CoFe2O4 with 2 nm CoFe2O4 (shell) and core size of 8 nm increased from 220 to 460 W/g (for 800 Oe). These exchange-coupled Fe3O4/CoFe2O4 core/shell nanoparticles can be a good candidate for advanced hyperthermia application.

Sustainable solid-state strategy to hierarchical core-shell structured Fe 3 O 4 @graphene towards a safer and green sodium ion full battery

KAUST Repository

Ding, Xiang; Huang, Xiaobing; Jin, Junling; Ming, Hai; Wang, Limin; Ming, Jun

2017-01-01

A sustainable solid-state strategy of SPEX milling is developed to coat metal oxide (e.g., Fe3O4) with tunable layers of graphene, and a new hierarchical core-shell structured Fe3O4@graphene composite is constructed. The presented green process can

Amperometric glucose sensor based on enhanced catalytic reduction of oxygen using glucose oxidase adsorbed onto core-shell Fe3O4-silica-Au magnetic nanoparticles

International Nuclear Information System (INIS)

Wang Aijun; Li Yongfang; Li Zhonghua; Feng Jiuju; Sun Yanli; Chen Jianrong

2012-01-01

Monodisperse Fe 3 O 4 magnetic nanoparticles (NPs) were prepared under facile solvothermal conditions and successively functionalized with silica and Au to form core/shell Fe 3 O 4 -silica-Au NPs. Furthermore, the samples were used as matrix to construct a glucose sensor based on glucose oxidase (GOD). The immobilized GOD retained its bioactivity with high protein load of 3.92 × 10 −9 mol·cm −2 , and exhibited a surface-controlled quasi-reversible redox reaction, with a fast heterogeneous electron transfer rate of 7.98 ± 0.6 s −1 . The glucose biosensor showed a broad linear range up to 3.97 mM with high sensitivity of 62.45 μA·mM −1 cm −2 and fast response (less than 5 s). - Graphical abstract: Core-shell structured Fe 3 O 4 -silica-Au nanoparticles were prepared and used as matrix to construct an amperometric glucose sensor based on glucose oxidase, which showed broad linear range, high sensitivity, and fast response. Highlights: ► Synthesis of monodispersed Fe 3 O 4 nanoparticles. ► Fabrication of core/shell Fe 3 O 4 -silica-Au nanoparticles. ► Construction of a novel glucose sensor with wide linear range, high sensitivity and fast response.

Gold nanorod@iron oxide core-shell heterostructures: synthesis, characterization, and photocatalytic performance.

Science.gov (United States)

Li, Yue; Zhao, Junwei; You, Wenlong; Cheng, Danhong; Ni, Weihai

2017-03-17

Iron oxides are directly coated on the surface of cetyl-trimethylammonium bromide (CTAB)-capped gold nanorods (AuNRs) in aqueous solutions at room temperature, which results in AuNR@Fe 2 O 3 , AuNR@Fe 3 O 4 , and AuNR@Fe 2 O 3 @Fe 3 O 4 core-shell heterostructures. The iron oxide shells are uniform, smooth, with characteristic porous structure, and their thickness can be readily tuned. The shell formation is highly dependent on the reaction parameters including pH and CTAB concentration. The Fe 2 O 3 shell is amorphous and exhibits nearly zero remanence and coercivity, while the Fe 3 O 4 shell is ferromagnetic with a low saturation magnetization of about 0.5 emu g -1 due to its low crystallinity and the porous structure. At elevated temperatures achieved by plasmonic heating of the Au core, the Fe 2 O 3 shell transforms from amorphous to γ-Fe 2 O 3 and α-Fe 2 O 3 phases, while the Fe 3 O 4 phase disappears because of the oxidation of Fe 2+ . A 1.4-fold increase of photocatalytic performance is observed due to the plasmonic resonance provided by the Au core. The photocatalytic efficiency of Fe 3 O 4 is about 1.7-fold higher than Fe 2 O 3 as more surface defects are present on the Fe 3 O 4 shell, promoting the adsorption and activation of reagents on the surface during the catalytic reactions. This approach can be readily extended to other nanostructures including Au spherical nanoparticles and nanostars. These highly uniform and multifunctional core-shell heterostructures can be of great potential in a variety of energy, magnetic, and environment applications.

Highly efficient enrichment of low-abundance intact proteins by core-shell structured Fe3O4-chitosan@graphene composites.

Science.gov (United States)

Zhang, Peng; Fang, Xiaoni; Yan, Guoquan; Gao, Mingxia; Zhang, Xiangmin

2017-11-01

In proteomics research, the screening and monitoring of disease biomarkers is still a major challenge, mainly due to their low concentration in biological samples. However, the universal enrichment of intact proteins has not been further studied. In this work, we developed a Fe 3 O 4 -chitosan@graphene (Fe 3 O 4 -CS@G) core-shell composite to enrich low-abundance proteins from biological samples. Fe 3 O 4 -CS@G composite holds chitosan layer decorated Fe 3 O 4 core, which improves the hydrophilicity of materials greatly. Meanwhile, the graphene nanosheets shell formed via electrostatic assembly endows the composite with huge surface area (178m 2 /g). The good water dispersibility ensures the sufficient contact opportunities between graphene composites and proteins, and the large surface area provides enough adsorption sites for the enrichment of proteins. Using Fe 3 O 4 -CS@G, four standard proteins Cyt-c, BSA, Myo and OVA were enriched with better adsorption capacity and recovery rate, compared with previously reported magnetic graphene composites. Additionally, the mechanism of compared to" is corrected into "compared with". proteins adsorption on Fe 3 O 4 -CS@G was further studied, which indicates that hydrophobic and electrostatic interaction work together to facilitate the universal and efficient enrichment of proteins. Human plasma sample was employed to further evaluate the enrichment performance of Fe 3 O 4 -CS@G. Eventually, 123 proteins were identified from one of SAX fractions of human plasma, which is much better than commercial Sep-pak C18 enrichment column (39 proteins). All these outstanding performances suggest that Fe 3 O 4 -CS@G is an ideal platform for the enrichment of low-abundance intact proteins and thus holds great potential to facilitate the identification of biomarkers from biological samples in proteomics research. Copyright © 2017 Elsevier B.V. All rights reserved.

Steam reforming of bio-oil from coconut shell pyrolysis over Fe/olivine catalyst

International Nuclear Information System (INIS)

Quan, Cui; Xu, Shaoping; Zhou, Congcong

2017-01-01

Highlights: • Steam reforming of the actual bio-oil was investigated with Fe/olivine catalyst. • Most of phenols in bio-oil were converted into gas products. • A carbon conversion of 97.2% was obtained under optimized conditions. - Abstract: Catalytic steam reforming of coconut shell pyrolysis bio-oil over Fe/olivine catalyst was conducted in a fixed-bed quartz reactor. The effects of calcination temperature, iron loading, reaction temperature, steam to carbon ratio (S/C), bio-oil weight hourly space velocity (W b HSV) on gas composition and carbon conversion were investigated. The results indicate that Fe/olivine has good activity for steam reforming of bio-oil, the couple Fe 2+/3+ /Fe 2+ may be sufficiently efficient for C–C, C–O and C–H breaking. After steam reforming, most of the phenolics in pyrolysis oil are converted into light molecular compounds such as H 2 , CO, CO 2 , and CH 4 . The H 2 concentration and carbon conversion were enhanced by increasing reaction temperature from 750 to 800 °C and the S/C from 1.5 to 2, but decreased with increasing calcination temperature. In the W b HSV range of 0.5–0.6, the hydrogen concentration decreased obviously, whereas it decreased slightly by further increasing W b HSV. The highest hydrogen concentration of 47.6 vol% was obtained among the catalysts tested, and the best carbon conversion was 97.2% over 10% Fe/olivine catalyst under the reforming conditions of temperature = 800 °C, W b HSV = 0.5, S/C = 2.

Visible and IR photoluminescence of c-FeSi@a-Si core-shell nano-fibres produced by vapour transport

CSIR Research Space (South Africa)

Thabethe, S

2013-11-01

Full Text Available The procedures for the synthesis of amorphous e-FeSi/Si core–shell nanofibres by vapour transport in a CVD configuration are reported. Crystallite studies by the Williamson-Hall method show the sizes to be typically about 8.0 nm which agrees...

Magnetization reversal in textured Fe nanoparticles having different aspect ratios

International Nuclear Information System (INIS)

Garcia Sanchez, F.; Chubykalo-Fesenko, O.; Crespo, P.; Hernando, A.; Gonzalez, J.M.

2005-01-01

The use of micromagnetic models on the simulation of the magnetization reversal allows approaching the 'ad hoc' design of materials for particular applications. As an example of this and trying to identify a particulate system with reduced interparticle dipolar interactions, we report on the results of a study of the hysteretic properties of textured Fe particles having thicknesses of the order of the units of nanometre and in-plane dimensions from 400x30 to 400x250 nm. Our results show that for sufficiently wide particles the moment configurations at the remanence correspond to an outer shell where the moments are essentially oriented along the direction parallel to the particle surface (therefore minimizing the surface poles) and an inner core (having larger volume than the shell) in which the moments point along one of the two easiest crystallographic directions. The reversal field of the outer shell is larger than that of the core and consequently the latter coincides with the global particle coercivity

Core–shell structured FeSiAl/SiO{sub 2} particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} soft magnetic composite cores with tunable insulating layer thicknesses

Energy Technology Data Exchange (ETDEWEB)

Fan, Xi’an, E-mail: groupfxa@163.com [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Wang, Jian, E-mail: snove418562@163.com [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Wu, Zhaoyang, E-mail: wustwuzhaoyang@163.com [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Li, Guangqiang, E-mail: ligq-wust@mail.wust.edu.cn [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China)

2015-11-15

Graphical abstract: - Highlights: • FeSiAl/SiO{sub 2} core–shell particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} composite cores were prepared. • SiO{sub 2} surrounding FeSiAl were replaced by Al{sub 2}O{sub 3} during sintering process. • Fe{sub 3}Si particles were separated by Al{sub 2}O{sub 3} with tunable thickness in composite cores. • Fe{sub 3}Si/Al{sub 2}O{sub 3} had lower core loss and better frequency stability than FeSiAl core. • The insulating layer between ferromagnetic particles can reduce core loss. - Abstract: FeSiAl/SiO{sub 2} core–shell particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} composite cores with tunable insulating layer thicknesses have been synthesized via a modified Stöber method combined with following high temperature sintering process. Most of the conductive FeSiAl particles could be coated by insulating SiO{sub 2} using the modified Stöber method. During the sintering process, the reaction 4Al + 3SiO{sub 2} ≣ 2α-Al{sub 2}O{sub 3} + 3Si took place and the new Fe{sub 3}Si/Al{sub 2}O{sub 3} composite was formed. The Fe{sub 3}Si/Al{sub 2}O{sub 3} composite cores displayed more excellent soft magnetic properties, better frequency stability at high frequencies, much higher resistivity and lower core loss than the raw FeSiAl core. Based on this, several types of FeSiAl/SiO{sub 2} particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} composite cores with tunable insulating layer thicknesses were selectively prepared by simply varying TEOS contents. The thickness of Al{sub 2}O{sub 3} insulating layer and resistivity of Fe{sub 3}Si/Al{sub 2}O{sub 3} composite cores increased with increasing the TEOS contents, while the permeability and core loss changed in the opposite direction.

Potential use of SERS-assisted theranostic strategy based on Fe{sub 3}O{sub 4}/Au cluster/shell nanocomposites for bio-detection, MRI, and magnetic hyperthermia

Energy Technology Data Exchange (ETDEWEB)

Han, Yu; Lei, Sheng-lan [Department of Biomaterials, College of Materials, Xiamen University, Xiamen 361005 (China); Lu, Jian-hua [Department of Electronic Science, College of Physical Science and Technology, Fujian Provincial Key Laboratory of Plasma and Magnetic Resonance Research, Xiamen University, Xiamen 361005 (China); He, Yuan [Department of Biomaterials, College of Materials, Xiamen University, Xiamen 361005 (China); Chen, Zhi-wei, E-mail: chenzhiwei@xmu.edu.cn [Department of Electronic Science, College of Physical Science and Technology, Fujian Provincial Key Laboratory of Plasma and Magnetic Resonance Research, Xiamen University, Xiamen 361005 (China); Ren, Lei, E-mail: renlei@xmu.edu.cn [Department of Biomaterials, College of Materials, Xiamen University, Xiamen 361005 (China); State Key Laboratory for Physical Chemistry of Solid Surfaces, Xiamen University, Xiamen 361005 (China); Fujian Collaborative Innovation Center for Exploitation and Utilization of Marine Biological Resources, Xiamen 361005 (China); Zhou, Xi [Department of Biomaterials, College of Materials, Xiamen University, Xiamen 361005 (China); Fujian Provincial Key Laboratory of Fire Retardant Materials, Xiamen University, Xiamen 361005 (China); Fujian Collaborative Innovation Center for Exploitation and Utilization of Marine Biological Resources, Xiamen 361005 (China)

2016-07-01

A surface-enhanced Raman scattering (SERS)-assisted theranostic strategy was designed based on a synthesized multifunctional Fe{sub 3}O{sub 4}/Au cluster/shell nanocomposite. This theranostic strategy was used for free prostate specific antigen (free-PSA) detection, magnetic resonance imaging (MRI), and magnetic hyperthermia. The lowest protein concentration detected was 1 ng mL{sup −1}, and the limit of detection (LOD) of the calculated PSA was 0.75 ng mL{sup −1}. Then, MRI was carried out to visualize the tumor cell. Lastly, magnetic hyperthermia was employed and revealed a favorable killing effect for the tumor cells. Thus, this SERS-assisted strategy based on a Fe{sub 3}O{sub 4}/Au cluster/shell nanocomposite showed great advantages in theranostic treatment. - Graphical abstract: Fe{sub 3}O{sub 4}/Au cluster/shell composite can be used for specific protein detection, magnetic resonance imaging and magnetic hyperthermia therapy. - Highlights: • We designed a SERS-assisted theranostic strategy based on the mutifunctional nanocomposites using gold shelled Fe{sub 3}O{sub 4} clusters. • Fe{sub 3}O{sub 4}/Au nanoparticles with theranostics and SERS for early diagnosis of PSA were reported for the first time. • The LOD of detection for PSA was lowed as 0.75 ng mL{sup −1}, and the total detection time was shorten to less than 1 h. • Fe{sub 3}O{sub 4} clusters had spin-spin (T{sub 2}) contrast enhancement and increased magnetic response. • Gold nanoshells supplied excellent chemical stability, biocompatibility, better heating property for magnetic hyperthermia.

Three-dimensional core-shell Fe_2O_3 @ carbon/carbon cloth as binder-free anode for the high-performance lithium-ion batteries

International Nuclear Information System (INIS)

Wang, Xiaohua; Zhang, Miao; Liu, Enzuo; He, Fang; Shi, Chunsheng; He, Chunnian; Li, Jiajun; Zhao, Naiqin

2016-01-01

Highlights: • The 3D core-shell Fe_2O_3@C/CC structure is fabricated by simple hydrothermal route. • The composite connected 3D carbon networks consist of carbon cloth, Fe_2O_3 nanorods and outer carbon layer. • The Fe_2O_3@C/CC used as binder-free anode in LIBs, demonstrates excellent performances. - Abstract: A facile and scalable strategy is developed to fabricate three dimensional core-shell Fe_2O_3 @ carbon/carbon cloth structure by simple hydrothermal route as binder-free lithium-ion battery anode. In the unique structure, carbon coated Fe_2O_3 nanorods uniformly disperse on carbon cloth which forms the conductive carbon network. The hierarchical porous Fe_2O_3 nanorods in situ grown on the carbon cloth can effectively shorten the transfer paths of lithium ions and reduce the contact resistance. The carbon coating significantly inhibits pulverization of active materials during the repeated Li-ion insertion/extraction, as well as the direct exposure of Fe_2O_3 to the electrolyte. Benefiting from the structural integrity and flexibility, the nanocomposites used as binder-free anode for lithium-ion batteries, demonstrate high reversible capacity and excellent cyclability. Moreover, this kind of material represents an alternative promising candidate for flexible, cost-effective, and binder-free energy storage devices.

Preparation of raspberry-like γ-Fe2O3/crackled nitrogen-doped carbon capsules and their application as supports to improve catalytic activity.

Science.gov (United States)

Zhang, Junshuai; Yao, Tongjie; Zhang, Hui; Zhang, Xiao; Wu, Jie

2016-11-10

In this manuscript, we have introduced a novel method to improve the catalytic activity of metal nanoparticles via optimizing the support structure. To this end, raspberry-like γ-Fe 2 O 3 /crackled nitrogen-doped carbon (CNC) capsules were prepared by a two-step method. Compared with traditional magnetic capsules, in γ-Fe 2 O 3 /CNC capsules, the γ-Fe 2 O 3 nanoparticles were embedded in a CNC shell; therefore, they neither occupied the anchoring sites for metal nanoparticles nor came into contact with them, which was beneficial for increasing the metal nanoparticle loading. Numerous tiny cracks appeared on the porous CNC shell, which effectively improved the mass diffusion and transport in catalytic reactions. Additionally, the coordination interaction could be generated between the precursor metal ions and doped-nitrogen atoms in the capsule shell. With the help of these structural merits, γ-Fe 2 O 3 /CNC capsules were ideal supports for Pd nanoparticles, because they were beneficial for improving the Pd loading, reducing the nanoparticle size, increasing their dispersity and maximizing the catalytic performance of Pd nanoparticles anchored on the inner shell surface. As expected, γ-Fe 2 O 3 /CNC@Pd catalysts exhibited a dramatically enhanced catalytic activity towards hydrophilic 4-nitrophenol and hydrophobic nitrobenzene. The reaction rate constant k was compared with recent work and the corresponding reference samples. Moreover, they could be easily recycled by using a magnet and reused without an obvious loss of catalytic activity.

Fabrication of Magnetite/Silica/Titania Core-Shell Nanoparticles

Directory of Open Access Journals (Sweden)

Suh Cem Pang

2012-01-01

Full Text Available Fe3O4/SiO2/TiO2 core-shell nanoparticles were synthesized via a sol-gel method with the aid of sonication. Fe3O4 nanoparticles were being encapsulated within discrete silica nanospheres, and a layer of TiO2 shell was then coated directly onto each silica nanosphere. As-synthesized Fe3O4/SiO2/TiO2 core-shell nanoparticles showed enhanced photocatalytic properties as evidenced by the enhanced photodegradation of methylene blue under UV light irradiation.

Fluoride adsorption from aqueous solution by magnetic core-shell Fe{sub 3}O{sub 4}@alginate-La particles fabricated via electro-coextrusion

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yahui [School of Materials Science and Engineering, Southwest University of Science and Technology, Mianyang 621010, Sichuan (China); Engineering Research Center of Biomass Materials, Ministry of Education, Mianyang 621010, Sichuan (China); Lin, Xiaoyan, E-mail: lxy20100205@163.com [School of Materials Science and Engineering, Southwest University of Science and Technology, Mianyang 621010, Sichuan (China); Engineering Research Center of Biomass Materials, Ministry of Education, Mianyang 621010, Sichuan (China); Zhou, Quisheng [A State Key Laboratory of Pulp & Paper Engineering, South China University of Technology, Guangzhou 510640 (China); Luo, Xuegang [Engineering Research Center of Biomass Materials, Ministry of Education, Mianyang 621010, Sichuan (China)

2016-12-15

Graphical abstract: The magnetic core-shell Fe{sub 3}O{sub 4}@Alg-La particles were fabricated successfully by a simple method of electro-coextrusion, and employed as an adsorbent for separation of fluoride from aqueous solution. - Highlights: • Magnetic core-shell Fe{sub 3}O{sub 4}@Alg-La particles were prepared by electro-coextrusion. • The maximum adsorption capacity for fluoride at 298.15 K was 45.230 mg/g. • The adsorbent has a good saturation magnetization value. • The adsorbent has a great potential in removing the fluoride. - Abstract: The magnetic core-shell Fe{sub 3}O{sub 4}@Alg-La particles were fabricated successfully by a simple method of electro-coextrusion, and employed as an adsorbent for separation of fluoride from aqueous solution. Main factors affecting the removal of fluoride, including pH, adsorbent dosage, initial concentration, temperature and contact time were investigated. The adsorption isotherm and adsorption kinetics were studied to understand the adsorption process in detail. The experimental data were fitted well by the non-linear Freundlich isotherm and linear pseudo-second-order model, the maximum fluoride adsorption capacity was 45.230 mg/g at pH 4, 298.15 K. Thermodynamic parameters indicated that the fluoride adsorption process was feasible and spontaneous. The presence of other anions like Cl{sup −}, SO{sub 4}{sup 2−}, HCO{sub 3}{sup −} and PO{sub 4}{sup 3−} had almost no effect on the fluoride adsorption. The adsorbent can be easily separated from the solution by a magnet. The magnetic core-shell Fe{sub 3}O{sub 4}@Alg-La particles before and after fluoride adsorption were studied by SEM, FTIR, EDX and XPS, which indicated that the adsorption mechanism may be related to electrostatic attraction and Lewis acid-base interaction.

Fe3O4@polyaniline yolk–shell micro/nanospheres as bifunctional materials for lithium storage and electromagnetic wave absorption

DEFF Research Database (Denmark)

Wang, Xiaoliang; Zhang, Minwei; Zhao, Jianming

2017-01-01

Unique Fe3O4/polyaniline (PANI) composite with yolk-shell micro/nanostructure (FPys) has been successfully synthesized by a facile silica-assisted in-situ polymerization and subsequent etching strategy. The structural and compositional studies of the FPys composites are performed by employing X......-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). The yolk-shell morphology of the products is confirmed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) observations. When evaluated as anode material for lithium-ion batteries, the as-prepared FPys electrodes...

Morphology and electronic structure of the oxide shell on the surface of iron nanoparticles.

Science.gov (United States)

Wang, Chongmin; Baer, Donald R; Amonette, James E; Engelhard, Mark H; Antony, Jiji; Qiang, You

2009-07-01

An iron (Fe) nanoparticle exposed to air at room temperature will be instantly covered by an oxide shell that is typically approximately 3 nm thick. The nature of this native oxide shell, in combination with the underlying Fe(0) core, determines the physical and chemical behavior of the core-shell nanoparticle. One of the challenges of characterizing core-shell nanoparticles is determining the structure of the oxide shell, that is, whether it is FeO, Fe(3)O(4), gamma-Fe(2)O(3), alpha-Fe(2)O(3), or something else. The results of prior characterization efforts, which have mostly used X-ray diffraction and spectroscopy, electron diffraction, and transmission electron microscopic imaging, have been framed in terms of one of the known Fe-oxide structures, although it is not necessarily true that the thin layer of Fe oxide is a known Fe oxide. In this Article, we probe the structure of the oxide shell on Fe nanoparticles using electron energy loss spectroscopy (EELS) at the oxygen (O) K-edge with a spatial resolution of several nanometers (i.e., less than that of an individual particle). We studied two types of representative particles: small particles that are fully oxidized (no Fe(0) core) and larger core-shell particles that possess an Fe core. We found that O K-edge spectra collected for the oxide shell in nanoparticles show distinct differences from those of known Fe oxides. Typically, the prepeak of the spectra collected on both the core-shell and the fully oxidized particles is weaker than that collected on standard Fe(3)O(4). Given the fact that the origin of this prepeak corresponds to the transition of the O 1s electron to the unoccupied state of O 2p hybridized with Fe 3d, a weak pre-edge peak indicates a combination of the following four factors: a higher degree of occupancy of the Fe 3d orbital; a longer Fe-O bond length; a decreased covalency of the Fe-O bond; and a measure of cation vacancies. These results suggest that the coordination configuration in

Modified ferrite core-shell nanoparticles magneto-structural characterization

Science.gov (United States)

Klekotka, Urszula; Piotrowska, Beata; Satuła, Dariusz; Kalska-Szostko, Beata

2018-06-01

In this study, ferrite nanoparticles with core-shell structures and different chemical compositions of both the core and shell were prepared with success. Proposed nanoparticles have in the first and second series magnetite core, and the shell is composed of a mixture of ferrites with Fe3+, Fe2+ and M ions (where M = Co2+, Mn2+ or Ni2+) with a general composition of M0.5Fe2.5O4. In the third series, the composition is inverted, the core is composed of a mixture of ferrites and as a shell magnetite is placed. Morphology and structural characterization of nanoparticles were done using Transmission Electron Microscopy (TEM), X-ray diffraction (XRD), and Infrared spectroscopy (IR). While room temperature magnetic properties were measured using Mössbauer spectroscopy (MS). It is seen from Mössbauer measurements that Co always increases hyperfine magnetic field on Fe atoms at RT, while Ni and Mn have opposite influences in comparison to pure Fe ferrite, regardless of the nanoparticles structure.

Nafion covered core–shell structured Fe{sub 3}O{sub 4}@graphene nanospheres modified electrode for highly selective detection of dopamine

Energy Technology Data Exchange (ETDEWEB)

Zhang, Wuxiang; Zheng, Jianzhong; Shi, Jiangu; Lin, Zhongqiu; Huang, Qitong; Zhang, Hanqiang; Wei, Chan [College of Chemistry and Environment, Minnan Normal University, Zhangzhou 363000 (China); Chen, Jianhua [College of Chemistry and Environment, Minnan Normal University, Zhangzhou 363000 (China); Fujian Province University Key Laboratory of Analytical Science, Minnan Normal University, Zhangzhou 363000 (China); Hu, Shirong, E-mail: Hushirong6666@163.com [College of Chemistry and Environment, Minnan Normal University, Zhangzhou 363000 (China); Fujian Province University Key Laboratory of Analytical Science, Minnan Normal University, Zhangzhou 363000 (China); School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100 (China); Hao, Aiyou [School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100 (China)

2015-01-01

Graphical abstract: Schematic illustration of the reaction mechanism of Fe{sub 3}O{sub 4}@GNs/Nafion with DA. - Highlights: • The sensor based on Fe{sub 3}O{sub 4}@graphene nanospheres was prepared for the first time. • The biosensor shows a wide linear range and a lower detection limit of 0.007 μM. • This method was successfully applied to detection of DA in real samples. - Abstract: Nafion covered core–shell structured Fe{sub 3}O{sub 4}@graphene nanospheres (GNs) modified glassy carbon electrode (GCE) was successfully prepared and used for selective detection dopamine. Firstly, the characterizations of hydro-thermal synthesized Fe{sub 3}O{sub 4}@GNs were investigated by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Raman spectroscopy. Then Fe{sub 3}O{sub 4}@GNs/Nafion modified electrode exhibited excellent electrocatalytic activity toward the oxidations of dopamine (DA). The interference test showed that the coexisted ascorbic acid (AA) and uric acid (UA) had no electrochemical interference toward DA. Under the optimum conditions, the broad linear relationship was obtained in the experimental concentration from 0.020 μM to 130.0 μM with the detection limit (S/N = 3) of 0.007 μM. Furthermore, the core–shell structured Fe{sub 3}O{sub 4}@GNs/Nafion/GCE was applied to the determination of DA in real samples and satisfactory results were got, which could provide a promising platform to develop excellent biosensor for detecting DA.

Improved atomic data for electron-transport predictions by the codes TIGER and TIGERP. I. Inner-shell ionization by electron collision

International Nuclear Information System (INIS)

Peek, J.M.; Halbleib, J.A.

1983-01-01

The inner-shell ionization data for electron-target collisions now in use in the TIGER and TIGERP electron-transport codes are extracted and compared with other data for these processes. The TIGER cross sections for K-shell ionization by electron collisions are found to be seriously in error for large-Z targets and incident electron energies greater than 1 MeV. A series of TIGER and TIGERP runs were carried out with and without improved K-shell electron ionization cross section data replacing that now in use. The relative importance of electron-impact and photon ionization of the various subshells was also extracted from these runs. In general, photon ionization dominated in the examples studied so the sensitivity of many predicted properties to errors in the electron-impact subshell ionization data was not large. However, some differences were found and, as all possible applications were not covered in this study, it is recommended that these electron-impact data now in TIGER and TIGERP be replaced. Cross section data for the processes under study are reviewed and those that are most suitable for this application are identified. 19 references, 9 figures, 2 tables

[Adsorption of Cu on Core-shell Structured Magnetic Particles: Relationship Between Adsorption Performance and Surface Properties].

Science.gov (United States)

Li, Qiu-mei; Chen, Jing; Li, Hai-ning; Zhang, Xiao-lei; Zhang, Gao-sheng

2015-12-01

In order to reveal the relationship between the adsorption performance of adsorbents and their compositions, structure, and surface properties, the core-shell structured Fe₃O₄/MnO2 and Fe-Mn/Mn₂2 magnetic particles were systematically characterized using multiple techniques and their Cu adsorption behaviors as well as mechanism were also investigated in details. It was found that both Fe₃O4 and Fe-Mn had spinel structure and no obvious crystalline phase change was observed after coating with MnO₂. The introduction of Mn might improve the affinity between the core and the shell, and therefore enhanced the amount and distribution uniformity of the MnO₂ coated. Consequently, Fe-Mn/MnO₂ exhibited a higher BET specific surface area and a lower isoelectric point. The results of sorption experiments showed that Fe-Mn had a higher maximal Cu adsorption capacity of 33.7 mg · g⁻¹ at pH 5.5, compared with 17.5 mg · g⁻¹ of Fe₃O4. After coating, the maximal adsorption capacity of Fe-Mn/MnO₂ was increased to 58.2 mg · g⁻¹, which was 2.6 times as high as that of Fe₃O₄/MnO₂ and outperformed the majority of magnetic adsorbents reported in literature. In addition, a specific adsorption of Cu occurred at the surface of Fe₃O₄/MnO₂ or Fe-Mn/MnO₂ through the formation of inner-sphere complexes. In conclusion, the adsorption performance of the magnetic particles was positively related to their compositions, structure, and surface properties.

High Photocatalytic Activity of Fe3O4-SiO2-TiO2 Functional Particles with Core-Shell Structure

Directory of Open Access Journals (Sweden)

Chenyang Xue

2013-01-01

Full Text Available This paper describes a novel method of synthesizing Fe3O4-SiO2-TiO2 functional nanoparticles with the core-shell structure. The Fe3O4 cores which were mainly superparamagnetic were synthesized through a novel carbon reduction method. The Fe3O4 cores were then modified with SiO2 and finally encapsulated with TiO2 by the sol-gel method. The results of characterizations showed that the encapsulated 700 nm Fe3O4-SiO2-TiO2 particles have a relatively uniform size distribution, an anatase TiO2 shell, and suitable magnetic properties for allowing collection in a magnetic field. These magnetic properties, large area, relative high saturation intensity, and low retentive magnetism make the particles have high dispersibility in suspension and yet enable them to be recovered well using magnetic fields. The functionality of these particles was tested by measuring the photocatalytic activity of the decolouring of methyl orange (MO and methylene blue (MB under ultraviolet light and sunlight. The results showed that the introduction of the Fe3O4-SiO2-TiO2 functional nanoparticles significantly increased the decoloration rate so that an MO solution at a concentration of 10 mg/L could be decoloured completely within 180 minutes. The particles were recovered after utilization, washing, and drying and the primary recovery ratio was 87.5%.

Fe-N and (Fe, Ni)-N Fine Powders for Magnetic Recording

International Nuclear Information System (INIS)

Chen Ziyu; Li Fashen

1998-01-01

Combining Moessbauer spectroscopy with magnetic property measurement, we have studied Fe-N and (Fe, Ni)-N powders for magnetic recording. The typical particles of the core (α-Fe)/shell (γ'-Fe 4 N) structure have been successfully prepared. All the products are stabilized in a multi-organic solution. It has been found that the coercivity can be changed from 300 to 800 Oe by adjusting the shape of the particles. The special saturation magnetization of the particles can be adjusted from 120 to 180emu/g and their chemical stability is improved by substituting nickel for iron in γ'-Fe 4 N. Following experiments for corrosion resistance, it is expected that (Fe, Ni)-N and the core/shell particles will be applied as recording media in the near future

Fe-N and (Fe, Ni)-N Fine Powders for Magnetic Recording

Energy Technology Data Exchange (ETDEWEB)

Chen Ziyu; Li Fashen [Lanzhou University, Department of Physics (China)

1998-12-15

Combining Moessbauer spectroscopy with magnetic property measurement, we have studied Fe-N and (Fe, Ni)-N powders for magnetic recording. The typical particles of the core ({alpha}-Fe)/shell ({gamma}'-Fe{sub 4}N) structure have been successfully prepared. All the products are stabilized in a multi-organic solution. It has been found that the coercivity can be changed from 300 to 800 Oe by adjusting the shape of the particles. The special saturation magnetization of the particles can be adjusted from 120 to 180emu/g and their chemical stability is improved by substituting nickel for iron in {gamma}'-Fe{sub 4}N. Following experiments for corrosion resistance, it is expected that (Fe, Ni)-N and the core/shell particles will be applied as recording media in the near future.

Pump requirements for betatron-generated femtosecond X-ray laser at saturation from inner-shell transitions

International Nuclear Information System (INIS)

Ribiere, M.; Grunenwald, J.; Ribeiro, P.; Sebban, S.; Phuoc, K.Ta; Gautier, J.; Kozlova, M.; Zeitoun, P.; Rousse, A.; Jacquemot, S.; Cheron, B.G.

2012-01-01

We study pump requirements to produce femtosecond X-ray laser pulses at saturation from inner-shell transitions in the amplified spontaneous emission regime. Since laser-based betatron radiation is considered as the pumping source, we first study the impact of the driving laser power on its intensity. Then we investigate the amplification behavior of the K-a transition of nitrogen at 3.2 nm (395 eV) from radiative transfer calculations coupled with kinetics modeling of the ion population densities. We show that the saturation regime may be experimentally achieved by using PW-class laser-accelerated electron bunches. Finally, we show that this X-ray laser scheme can be extended to heavier atoms and we calculate pump requirements to reach saturation at 1.5 nm (849 eV) from the K-a transition of neon. (authors)

Inner shell ionization by incident nuclei

International Nuclear Information System (INIS)

Hansteen, J.M.

1974-10-01

The atomic Coulomb excitation process induced by impinging heavy charged particles such as protons, deuterons, α-particles and complex heavy ions is reviewed. Recent experimental and theoretical efforts have led toimproved understanding of the atomic Coulomb excitation as well as to discovery of new types of ionization mechanisms. The following models are mentioned: the Plane Wave Born Approximation (PWBA); theeeeeeeeeeeee modified PWBA model; the Binary Encounter Approximation (BEA); the Semi-Classical Approximation (SCA); the Perturbed-Stationary-State model (PSS). The structure of the SCA model is more thoroughly treated. Experimental results on single Coulomb ionizations of the K-, L-, and M-shells, and of the connected sub-shells by protons are compared with predictions. Most calculations are based on straight line projectile paths and non-relativistic hydrogen-like target electron wave functions. The BEA model and the SCA model seem to work reasonably well for multiple Coulomb ionizations by stripped light ions. Background effects in ion-atom collisions are commented upon. Future aspects of atomic Coulomb excitation by incident nuclei and ions are discussed. The interplay between Coulomb induced processes and united atom phenomena is especially mentioned. The simple ionization models have yielded valuable insights but it is suggested that this branch of collision physics has reached a turning point where new and more advanced and unifying models are needed. (JIW)

Structural and magnetic properties of core-shell iron-iron oxide nanoparticles

DEFF Research Database (Denmark)

Kuhn, Luise Theil; Bojesen, A.; Timmermann, L.

2002-01-01

We present studies of the structural and magnetic properties of core-shell iron-iron oxide nanoparticles. alpha-Fe nanoparticles were fabricated by sputtering and subsequently covered with a protective nanocrystalline oxide shell consisting of either maghaemite (gamma-Fe2O3) or partially oxidized...... magnetite (Fe3O4). We observed that the nanoparticles were stable against further oxidation, and Mossbauer spectroscopy at high applied magnetic fields and low temperatures revealed a stable form of partly oxidized magnetite. The nanocrystalline structure of the oxide shell results in strong canting...... of the spin structure in the oxide shell, which thereby modifies the magnetic properties of the core-shell nanoparticles....

Synthesis of MnFe2O4@Mn-Co oxide core-shell nanoparticles and their excellent performance for heavy metal removal.

Science.gov (United States)

Ma, Zichuan; Zhao, Dongyuan; Chang, Yongfang; Xing, Shengtao; Wu, Yinsu; Gao, Yuanzhe

2013-10-21

Magnetic nanomaterials that can be easily separated and recycled due to their magnetic properties have received considerable attention in the field of water treatment. However, these nanomaterials usually tend to aggregate and alter their properties. Herein, we report an economical and environmentally friendly method for the synthesis of magnetic nanoparticles with core-shell structure. MnFe2O4 nanoparticles have been successfully coated with amorphous Mn-Co oxide shells. The synthesized MnFe2O4@Mn-Co oxide nanoparticles have highly negatively charged surface in aqueous solution over a wide pH range, thus preventing their aggregation and enhancing their performance for heavy metal cation removal. The adsorption isotherms are well fitted to a Langmuir adsorption model, and the maximal adsorption capacities of Pb(II), Cu(II) and Cd(II) on MnFe2O4@Mn-Co oxide are 481.2, 386.2 and 345.5 mg g(-1), respectively. All the metal ions can be completely removed from the mixed metal ion solutions in a short time. Desorption studies confirm that the adsorbent can be effectively regenerated and reused.

Absolute cross-section measurements of inner-shell ionization

Science.gov (United States)

Schneider, Hans; Tobehn, Ingo; Ebel, Frank; Hippler, Rainer

1994-12-01

Cross section ratios for K- and L-shell ionization of thin silver and gold targets by positron and electron impact have been determined at projectile energies of 30 70 keV. The experimental results are confirmed by calculations in plane wave Born approximation (PWBA) which include an electron exchange term and account for the deceleration or acceleration of the incident projectile in the nuclear field of the target atom. We report first absolute cross sections for K- and L-shell ionization of silver and gold targets by lepton impact in the threshold region. We have measured the corresponding cross sections for electron (e-) impact with an electron gun and the same experimental set-up.

Application of Fe3O4@MIL-100 (Fe) core-shell magnetic microspheres for evaluating the sorption of organophosphate esters to dissolved organic matter (DOM).

Science.gov (United States)

Pang, Long; Yang, Peijie; Yang, Huiqiang; Ge, Liming; Xiao, Jingwen; Zhou, Yifan

2018-06-01

Organophosphate esters (OPEs) are widely used as flame retardants and plasticizers in many products and materials. Because of the potential biologic toxicity on human beings, OPEs are regarded as a class of emerging pollutants. Dissolved organic matters (DOM) have significant effects on the bioavailability and toxicity of the pollutants in the environment. Negligible-depletion solid-phase microextraction (nd-SPME) is an efficient way for measuring the freely dissolved pollutants but suffers from long equilibrium time. Metal-organic frameworks (MOFs) are a class of porous crystalline materials with unique properties such as high pore volume, regular porosity, and tunable pore size, being widely used for the extraction of various organic compounds. Here we developed a novel method for quick determination the sorption coefficients of OPEs to DOM in aquatic phase using Fe 3 O 4 @MIL-100 (Fe) core-shell magnetic microspheres. The mesoporous structures of the as-synthesized microspheres hindered the extraction of OPEs which associated with humic acid due to the volume exclusion effect. However, the freely dissolved OPEs can access into the mesoporous and then were extracted by MIL-100 (Fe). Due to the small pore size (4.81 nm), large surface area (141 m 2  g -1 ), high pore volume (0.17 g 3  g -1 ), and ultra-thin MOFs layers, Fe 3 O 4 @MIL-100 (Fe) core-shell magnetic microspheres have large contact area for the analytes in aqueous phase and therefore the diffusion distance was largely shortened. Besides, the microspheres can be collected conveniently after the extraction process by applying a magnetic field. Compared to the nd-SPME method with 35 h equilibration time (t 90% ), the proposed method for these studied OPEs only need 24 min to achieve equilibration. The sorption coefficients (logK DOC ) of the OPEs to humic acid were ranged from 3.84-5.28, which were highly consistent with the results by using polyacrylate-coated fiber and polydimethylsiloxane

Improved electrochemical performance of porous Fe{sub 3}O{sub 4}/carbon core/shell nanorods as an anode for lithium-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Xiong, Q.Q.; Lu, Y. [State Key Laboratory of Silicon Materials and Department of Materials Science and Engineering, Zhejiang University, Hangzhou 310027 (China); Wang, X.L., E-mail: wangxl@zju.edu.cn [State Key Laboratory of Silicon Materials and Department of Materials Science and Engineering, Zhejiang University, Hangzhou 310027 (China); Gu, C.D.; Qiao, Y.Q. [State Key Laboratory of Silicon Materials and Department of Materials Science and Engineering, Zhejiang University, Hangzhou 310027 (China); Tu, J.P., E-mail: tujp@zju.edu.cn [State Key Laboratory of Silicon Materials and Department of Materials Science and Engineering, Zhejiang University, Hangzhou 310027 (China)

2012-09-25

Highlights: Black-Right-Pointing-Pointer We prepared porous Fe{sub 3}O{sub 4}/C core/shell nanorods by a facile hydrothermal method using porous Fe{sub 2}O{sub 3} nanorods as the precursor. Black-Right-Pointing-Pointer The Fe{sub 3}O{sub 4}/C nanorods are homogenously coated by an amorphous carbon layer. Black-Right-Pointing-Pointer The Fe{sub 3}O{sub 4}/C nanorod electrode shows high capacity and good cycle stability, as well as enhanced rate performance. - Abstract: Porous Fe{sub 3}O{sub 4}/C core/shell nanorods have been prepared by a facile hydrothermal method using porous Fe{sub 2}O{sub 3} nanorods as the precursor and glucose as the carbon source. The Fe{sub 3}O{sub 4}/C nanorods possess a uniform size with 50-80 nm in diameter and 300-500 nm in length, and are homogenously coated by amorphous carbon layer. The porous nanorods greatly increase the electrical contact, thus facilitating the Li-ion and electron transportation, and enhancing the reactivity of the electrode. Also, the carbon layer can effectively limit the volume expansion and detachment of Fe{sub 3}O{sub 4}, and thus increase its structure stability during cycling. In the context of lithium storage behavior, the Fe{sub 3}O{sub 4}/C nanorod electrode shows high capacity and good cycle stability, as well as enhanced rate performance. After 50 cycles, the reversible capacity of the porous Fe{sub 3}O{sub 4}/C nanorods is 762.1 mAh g{sup -1} at 0.1 C and 597.2 mAh g{sup -1} at 0.5 C, much higher than that of {alpha}-Fe{sub 2}O{sub 3} nanorods (276.4 mAh g{sup -1}) and Fe{sub 3}O{sub 4} nanoparticles (307.9 mAh g{sup -1}). At a high rate of 1 C, the specific capacity of Fe{sub 3}O{sub 4}/C nanorods is still as high as 630.1 mAh g{sup -1}.

Magnetic response of hybrid ferromagnetic and antiferromagnetic core-shell nanostructures.

Science.gov (United States)

Khan, U; Li, W J; Adeela, N; Irfan, M; Javed, K; Wan, C H; Riaz, S; Han, X F

2016-03-21

The synthesis of FeTiO3-Ni(Ni80Fe20) core-shell nanostructures by a two-step method (sol-gel and DC electrodeposition) has been demonstrated. XRD analysis confirms the rhombohedral crystal structure of FeTiO3(FTO) with space group R3[combining macron]. Transmission electron microscopy clearly depicts better morphology of nanostructures with shell thicknesses of ∼25 nm. Room temperature magnetic measurements showed significant enhancement of magnetic anisotropy for the permalloy (Ni80Fe20)-FTO over Ni-FTO core-shell nanostructures. Low temperature magnetic measurements of permalloy-FeTiO3 core-shell structure indicated a strong exchange bias mechanism with magnetic coercivity below the antiferromagnetic Neel temperature (TN = 59 K). The exchange bias is attributed to the alignment of magnetic moments in the antiferromagnetic material at low temperature. Our scheme opens a path towards optimum automotive systems and wireless communications wherein broader bandwidths and smaller sizes are required.

Thick-shell nanocrystal quantum dots

Science.gov (United States)

Hollingsworth, Jennifer A [Los Alamos, NM; Chen, Yongfen [Eugene, OR; Klimov, Victor I [Los Alamos, NM; Htoon, Han [Los Alamos, NM; Vela, Javier [Los Alamos, NM

2011-05-03

Colloidal nanocrystal quantum dots comprising an inner core having an average diameter of at least 1.5 nm and an outer shell, where said outer shell comprises multiple monolayers, wherein at least 30% of the quantum dots have an on-time fraction of 0.80 or greater under continuous excitation conditions for a period of time of at least 10 minutes.

Measurements of inner-shell characteristic X-ray yields of thick W, Mo and Zr targets by low-energy electron impact and comparison with Monte Carlo simulations

International Nuclear Information System (INIS)

Li, X.L.; Zhao, J.L.; Tian, L.X.; An, Z.; Zhu, J.J.; Liu, M.T.

2014-01-01

Highlights: •We measured characteristic X-ray yields of thick W, Mo, Zr by 5–29 keV electrons. •Our measured data are in general in good agreement with the MC results with ∼10%. •Error of 10% of characteristic X-ray yields will produce errors of 2–7% for BIXS. -- Abstract: Inner-shell characteristic X-ray yields are one of the important ingredients in the β-ray induced X-ray spectrometry (BIXS) technique which can be used to perform tritium content and depth distribution analyses in plasma facing materials (PLMs) and other tritium-containing materials, such as W, Mo, Zr. In this paper, the measurements of K, L, M-shell X-ray yields Y(E) of pure thick W (Z = 74), Mo (Z = 42) and Zr (Z = 40) element targets produced by electron impact in the energy range of 5–29 keV are presented. The experimental data for Y(E) are compared with the corresponding predictions from Monte Carlo (MC) calculations using the general purpose MC code PENELOPE. In general, a good agreement is obtained between the experiment and the MC calculations for the variation of Y(E) with the impact energy both in shape and in magnitude with ∼10%. The effect of uncertainty of inner-shell characteristic X-ray yields on the BIXS technique is also discussed

Multifunctional Fe3O4 @ Au core/shell nanostars: a unique platform for multimode imaging and photothermal therapy of tumors

Science.gov (United States)

Hu, Yong; Wang, Ruizhi; Wang, Shige; Ding, Ling; Li, Jingchao; Luo, Yu; Wang, Xiaolin; Shen, Mingwu; Shi, Xiangyang

2016-01-01

We herein report the development of multifunctional folic acid (FA)-targeted Fe3O4 @ Au nanostars (NSs) for targeted multi-mode magnetic resonance (MR)/computed tomography (CT)/photoacoustic (PA) imaging and photothermal therapy (PTT) of tumors. In this present work, citric acid-stabilized Fe3O4/Ag composite nanoparticles prepared by a mild reduction route were utilized as seeds and exposed to the Au growth solution to induce the formation of Fe3O4 @ Au core/shell NSs. Followed by successive decoration of thiolated polyethyleneimine (PEI-SH), FA via a polyethylene glycol spacer, and acetylation of the residual PEI amines, multifunctional Fe3O4 @ Au NSs were formed. The designed multifunctional NSs possess excellent colloidal stability, good cytocompatibility in a given concentration range, and specific recognition to cancer cells overexpressing FA receptors. Due to co-existence of Fe3O4 core and star-shaped Au shell, the NSs can be used for MR and CT imaging of tumors, respectively. Likewise, the near infrared plasmonic absorption feature also enables the NSs to be used for PA imaging and PTT of tumors. Our study clearly demonstrates a unique theranostic nanoplatform that can be used for high performance multi-mode imaging-guided PTT of tumors, which may be extendable for theranostics of different diseases in translational medicine. PMID:27325015

Amperometric glucose sensor based on enhanced catalytic reduction of oxygen using glucose oxidase adsorbed onto core-shell Fe{sub 3}O{sub 4}-silica-Au magnetic nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Wang Aijun [College of Geography and Environmental Science, College of Chemistry and Life Science, Zhejiang Normal University, Jinhua 321004 (China); Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, School of Chemistry and Environmental Science, Henan Normal University, Xinxiang 453007 (China); Li Yongfang [College of Chemistry and Chemical Engineering, Henan Institute of Science and Technology, Xinxiang 453003 (China); Li Zhonghua [Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, School of Chemistry and Environmental Science, Henan Normal University, Xinxiang 453007 (China); Feng Jiuju, E-mail: jjfengnju@gmail.com [College of Geography and Environmental Science, College of Chemistry and Life Science, Zhejiang Normal University, Jinhua 321004 (China); Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, School of Chemistry and Environmental Science, Henan Normal University, Xinxiang 453007 (China); Sun Yanli [Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, School of Chemistry and Environmental Science, Henan Normal University, Xinxiang 453007 (China); Chen Jianrong [College of Geography and Environmental Science, College of Chemistry and Life Science, Zhejiang Normal University, Jinhua 321004 (China)

2012-08-01

Monodisperse Fe{sub 3}O{sub 4} magnetic nanoparticles (NPs) were prepared under facile solvothermal conditions and successively functionalized with silica and Au to form core/shell Fe{sub 3}O{sub 4}-silica-Au NPs. Furthermore, the samples were used as matrix to construct a glucose sensor based on glucose oxidase (GOD). The immobilized GOD retained its bioactivity with high protein load of 3.92 Multiplication-Sign 10{sup -9} mol{center_dot}cm{sup -2}, and exhibited a surface-controlled quasi-reversible redox reaction, with a fast heterogeneous electron transfer rate of 7.98 {+-} 0.6 s{sup -1}. The glucose biosensor showed a broad linear range up to 3.97 mM with high sensitivity of 62.45 {mu}A{center_dot}mM{sup -1} cm{sup -2} and fast response (less than 5 s). - Graphical abstract: Core-shell structured Fe{sub 3}O{sub 4}-silica-Au nanoparticles were prepared and used as matrix to construct an amperometric glucose sensor based on glucose oxidase, which showed broad linear range, high sensitivity, and fast response. Highlights: Black-Right-Pointing-Pointer Synthesis of monodispersed Fe{sub 3}O{sub 4} nanoparticles. Black-Right-Pointing-Pointer Fabrication of core/shell Fe{sub 3}O{sub 4}-silica-Au nanoparticles. Black-Right-Pointing-Pointer Construction of a novel glucose sensor with wide linear range, high sensitivity and fast response.

Synthesis, microstructure and magnetic properties of Fe{sub 3}Si{sub 0.7}Al{sub 0.3}@SiO{sub 2} core–shell particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} soft magnetic composite core

Energy Technology Data Exchange (ETDEWEB)

Wang, Jian, E-mail: snove418562@163.com [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Fan, Xi’an, E-mail: groupfxa@163.com [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Wu, Zhaoyang, E-mail: wustwuzhaoyang@163.com [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Li, Guangqiang [The State Key Laboratory of Refractories and Metallurgy, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China); Key Laboratory for Ferrous Metallurgy and Resources Utilization of Ministry of Education, Wuhan University of Science and Technology, Wuhan, Hubei 430081 (China)

2015-11-15

Fe{sub 3}Si{sub 0.7}Al{sub 0.3}@SiO{sub 2} core–shell particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} soft magnetic composite core have been synthesized via a modified stöber method combined with following high temperature sintering process. Most of conductive Fe{sub 3}Si{sub 0.7}Al{sub 0.3} particles could be uniformly coated by insulating SiO{sub 2} using the modified stöber method. The Fe{sub 3}Si{sub 0.7}Al{sub 0.3}@SiO{sub 2} core–shell particles exhibited good soft magnetic properties with low coercivity and high saturation magnetization. The reaction 4Al+3SiO{sub 2}=2α-Al{sub 2}O{sub 3}+3Si took place during the sintering process. As a result the new Fe{sub 3}Si/Al{sub 2}O{sub 3} composite was formed. The Fe{sub 3}Si/Al{sub 2}O{sub 3} composite core displayed more excellent soft magnetic properties, better frequency stability at high frequencies, much higher electrical resistivity and lower core loss than the pure Fe{sub 3}Si{sub 0.7}Al{sub 0.3} core. The method of introducing insulating layers surrounding magnetic particles provides a promising route to develop new and high compact soft magnetic materials with good magnetic and electric properties. - Graphical abstract: In Fe{sub 3}Si/Al{sub 2}O{sub 3} composite, Fe{sub 3}Si phases are separated by Al{sub 2}O{sub 3} layers and the eddy currents are confined in Fe{sub 3}Si phases, thus increasing resistivity and reducing core loss. - Highlights: • Fe{sub 3}Si{sub 0.7}Al{sub 0.3}@SiO{sub 2} core–shell particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} cores were prepared. • Fe{sub 3}Si{sub 0.7}Al{sub 0.3} particles could be uniformly coated by nano-sized SiO{sub 2} clusters. • Fe{sub 3}Si{sub 0.7}Al{sub 0.3}@SiO{sub 2} particles and Fe{sub 3}Si/Al{sub 2}O{sub 3} cores showed good soft magnetic properties. • Fe{sub 3}Si/Al{sub 2}O{sub 3} had lower core loss and better frequency stability than Fe{sub 3}Si{sub 0.7}Al{sub 0.3} cores.

Inner-shell photoionization in weak and strong radiation fields

International Nuclear Information System (INIS)

Southworth, S.H.; Dunford, R.W.; Ederer, D.L.; Kanter, E.P.; Kraessig, B.; Young, L.

2004-01-01

The X-ray beams presently produced at synchrotron-radiation facilities interact weakly with matter, and the observation of double photoionization is due to electron-electron interactions. The intensities of future X-ray free-electron lasers are expected to produce double photoionization by absorption of two photons. The example of double K-shell photoionization of neon is discussed in the one- and two-photon cases. We also describe an experiment in which X rays photoionize the K shell of krypton in the presence of a strong AC field imposed by an optical laser

A facile method for preparing porous, optically active, magnetic Fe3 O4 @poly(N-acryloyl-leucine) inverse core/shell composite microspheres.

Science.gov (United States)

Liu, Dong; Deng, Jianping; Yang, Wantai

2014-01-01

The first synthesis of porous, optically active, magnetic Fe3 O4 @poly(N-acryloyl-leucine) inverse core/shell composite microspheres is reported, in which the core is constructed of chiral polymer and the shell is constructed of Fe3 O4 NPs. The microspheres integrate three significant concepts, "porosity", "chirality", and "magneticity", in one single microspheric entity. The microspheres consist of Fe3 O4 nanoparticles and porous optically active microspheres, and thus combine the advantages of both magnetic nanoparticles and porous optically active microspheres. The pore size and specific surface area of the microspheres are characterized by N2 adsorption, from which it is found that the composite microspheres possess a desirable porous structure. Circular dichroism and UV-vis absorption spectroscopy measurements demonstrate that the microspheres exhibit the expected optical activity. The microspheres also have high saturation magnetization of 14.7 emu g(-1) and rapid magnetic responsivity. After further optimization, these novel microspheres may potentially find applications in areas such as asymmetric catalysis, chiral adsorption, etc. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Simple and efficient synthesis of copper(II)-modified uniform magnetic Fe3O4@SiO2 core/shell microspheres for immobilization of cellulase

Science.gov (United States)

Li, Shi-Kuo; Hou, Xiao-Cheng; Huang, Fang-Zhi; Li, Chuan-Hao; Kang, Wen-Juan; Xie, An-Jian; Shen, Yu-Hua

2013-11-01

In this paper, we reported a simple and efficient protocol for preparation of Cu2+-modified magnetic Fe3O4@SiO2 core/shell microspheres for immobilization of cellulase. The uniform magnetic Fe3O4@SiO2 core/shell microspheres with a thin shell of 20 nm were synthesized through a solvothermal method followed by a sol-gel process. An amino-terminated silane coupling agent of (3-aminopropyl)triethoxysilane (APTS) was then grafted on them for capturing Cu2+ ions. The reaction process is very simple, efficient, and economical. Noticeably, the content of Cu2+ ions on the magnetic core/shell microspheres can reach 4.6 Wt%, endowing them possess as high immobilization capacity as 225.5 mg/g for cellulase. And the immobilized cellulase can be retained over 90 % on the magnetic microspheres after six cycles. Meanwhile, the magnetic microspheres decorated with Cu2+ ions show a superparamagnetic character with a high magnetic saturation of 58.5 emu/g at room temperature, suggesting conveniently and rapidly recycle the enzyme from solution. This facile, recyclable, high immobilization capacity and activity strategy may find potential applications in enzyme catalytic reactions with low cost.

Simple and efficient synthesis of copper(II)-modified uniform magnetic Fe3O4@SiO2 core/shell microspheres for immobilization of cellulase

International Nuclear Information System (INIS)

Li, Shi-Kuo; Hou, Xiao-Cheng; Huang, Fang-Zhi; Li, Chuan-Hao; Kang, Wen-Juan; Xie, An-Jian; Shen, Yu-Hua

2013-01-01

In this paper, we reported a simple and efficient protocol for preparation of Cu 2+ -modified magnetic Fe 3 O 4 @SiO 2 core/shell microspheres for immobilization of cellulase. The uniform magnetic Fe 3 O 4 @SiO 2 core/shell microspheres with a thin shell of 20 nm were synthesized through a solvothermal method followed by a sol–gel process. An amino-terminated silane coupling agent of (3-aminopropyl)triethoxysilane (APTS) was then grafted on them for capturing Cu 2+ ions. The reaction process is very simple, efficient, and economical. Noticeably, the content of Cu 2+ ions on the magnetic core/shell microspheres can reach 4.6 Wt%, endowing them possess as high immobilization capacity as 225.5 mg/g for cellulase. And the immobilized cellulase can be retained over 90 % on the magnetic microspheres after six cycles. Meanwhile, the magnetic microspheres decorated with Cu 2+ ions show a superparamagnetic character with a high magnetic saturation of 58.5 emu/g at room temperature, suggesting conveniently and rapidly recycle the enzyme from solution. This facile, recyclable, high immobilization capacity and activity strategy may find potential applications in enzyme catalytic reactions with low cost

Parameterized Finite Element Modeling and Buckling Analysis of Six Typical Composite Grid Cylindrical Shells

Science.gov (United States)

Lai, Changliang; Wang, Junbiao; Liu, Chuang

2014-10-01

Six typical composite grid cylindrical shells are constructed by superimposing three basic types of ribs. Then buckling behavior and structural efficiency of these shells are analyzed under axial compression, pure bending, torsion and transverse bending by finite element (FE) models. The FE models are created by a parametrical FE modeling approach that defines FE models with original natural twisted geometry and orients cross-sections of beam elements exactly. And the approach is parameterized and coded by Patran Command Language (PCL). The demonstrations of FE modeling indicate the program enables efficient generation of FE models and facilitates parametric studies and design of grid shells. Using the program, the effects of helical angles on the buckling behavior of six typical grid cylindrical shells are determined. The results of these studies indicate that the triangle grid and rotated triangle grid cylindrical shell are more efficient than others under axial compression and pure bending, whereas under torsion and transverse bending, the hexagon grid cylindrical shell is most efficient. Additionally, buckling mode shapes are compared and provide an understanding of composite grid cylindrical shells that is useful in preliminary design of such structures.

Synthesis and characterization of thermal energy storage microencapsulated n-dodecanol with acrylic polymer shell

International Nuclear Information System (INIS)

Ma, Yanjie; Zong, Jiwen; Li, Wei; Chen, Long; Tang, Xiaofen; Han, Na; Wang, Jianping; Zhang, Xingxiang

2015-01-01

Two kinds of (microencapsulated phase change materials) MicroPCMs with acrylic-based copolymer as shell and n-dodecanol as core were successfully fabricated via suspension-like polymerization and photo-induced microencapsulation, respectively. Morphology and core–shell structure were observed by (field emission scanning electron microscope) FE-SEM. Thermal properties of the microencapsulated n-dodecanol were investigated by (differential scanning calorimeter) DSC and (thermogravimetric analysis) TGA. The results indicate that the mass ratio of core to shell has great influence on the morphology, inner structure, microencapsulated efficiency and durability of the microcapsules. Besides, the effects of various solvents and UV irridiation time on the microcapsule surface were discussed as well. In the experiment carried out, metal-ion complexation was conducted by the reaction between Mn ion and carboxyl groups on copolymer shell to enhance the performance of the microcapsules with n-dodecanol encapsulated. As the results indicate, the physicochemical properties and thermal conductivity of the shell were improved after Mn ion complexation reaction. Supercooling phenomenon of n-dodecanol was depressed to some extent. In the end, the thermo-regulated fiber containing acrylic-based copolymer microcapsules was fabricated, and thermo-regulated performance test of the fiber was also conducted. - Graphical abstract: (a)∼(d) schematic diagram of microencapsulation and (e) microcapsule with core–shell structure. - Highlights: • Microencapsulated n-dodecanol with acrylic polymer shell. • Microencapsulated n-dodecanol was fabricated by photo-induced microencapsulation. • Acrylic-based copolymer microcapsules with manganese-ion complexation

Effects of Coulomb repulsion in the inner-shell ionization cross-section by protons, deuterons and alpha-particles

International Nuclear Information System (INIS)

Magno, C.; Milazzo, M.; Pizzi, C.; Porro, F.; Rota, A.; Riccobono, G.

1979-01-01

A critical survey has been made of the currently accepted BEA theory for inner-shell atomic-ionization processes. This review has led to the introduction of an effective ion energy which accounts for the slowing-down of the ion in the nuclear Coulomb field. The effect of the ion deflection, also due to the nuclear Coulomb field, is analyzed. Relativistic effects in the collision of ions with K-shell electrons have been taken into account. A tentative qualitative explanation for the experimentally observed nonexistence of a threshold energy for ionization is given in the framework of the BEA theory. Ionization cross-sections for Rb, Sr, Zr, Cd, In, Sb, W by protons in the energy range from 500 keV to 3 MeV have been measured. Also measurements of ionization cross-sections by deuterons in the energy range from 800 keV to 2.6 MeV on Rb, Sr, Zr, Cd, Sb and by He ions in the energy range from 1.4 MeV to 2.8 MeV on Cd and Sb have been performed. Results are compared with those of other authors and in the context of the corrections introduced in the BEA theory. (author)

Synthesis and electrochemical properties of Fe_3O_4@MOF core-shell microspheres as an anode for lithium ion battery application

International Nuclear Information System (INIS)

Sun, Xuemin; Gao, Ge; Yan, Dongwei; Feng, Chuanqi

2017-01-01

Highlights: • Fe_3O_4 particles are encapsulated by HKUST-1 to form core-shell microspheres composite. • The composite exhibits outstanding electrochemical performances as a novel anode. • The typical approach can be used to prepare some novel electrode materials. - Abstract: The Fe_3O_4@MOF composite with a microspheric core and a porous metal-organic framework (MOF HKUST-1) shell has been successfully synthesized utilizing a versatile Layer-by-Layer (LBL) assembly method. The structure was identified by X-ray diffraction (XRD), and the morphology was investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques. The Fe_3O_4@MOF composite exhibited outstanding electrochemical properties when it was used as an anode material for lithium ion batteries (LIBs). After 100 discharge-charge cycles at a current density of 100 mA g"−"1, the reversible capacity of Fe_3O_4@MOF could maintain ∼1002 mAh g"−"1, which was much higher than that of the bare Fe_3O_4 counterpart (696 mAh g"−"1). Moreover, load the current density as high as 2 A g"−"1 (after 70 cycles at the current density step increased from 0.1 to 2 A g"−"1), it still delivered a reversible capacity of ∼429 mAh g"−"1. The results demonstrate that the cycling stability of Fe_3O_4 as an anode could be significantly improved by coating Cu_3(1,3,5-benzenetricarboxylate)_2 (HKUST-1). This strategy may offer new route to prepare other composite materials using different particles and suitable Metal-organic frameworks (MOFs) for LIBs application.

Esclavitud y ética comercial en el siglo XVI

Directory of Open Access Journals (Sweden)

Jörg Alejandro Tellkamp

2004-01-01

Full Text Available En varios tratados españoles del siglo XVI, la esclavitud como fenómeno social y comercial adquirió una importancia teórica cada vez mayor con respecto al estatus legal y moral de los seres humanos. El presente trabajo trata de esbozar algunos de los argumentos con respecto al comercio de esclavos y sus implicaciones morales y legales de acuerdo los autores Tomás de Mercado (1530-1576 y Bartolomé Frías de Albornoz (s. XVI, mostrando cómo la discusión se encaminó hacia la expresión de derechos individuales, sin, no obstante, superar el tradicional apego al concepto de esclavitud legal.

Three-dimensional core-shell Fe{sub 2}O{sub 3} @ carbon/carbon cloth as binder-free anode for the high-performance lithium-ion batteries

Energy Technology Data Exchange (ETDEWEB)

Wang, Xiaohua; Zhang, Miao [School of Materials Science and Engineering and Tianjin Key Laboratory of Composites and Functional Materials, Tianjin University, Tianjin 300350 (China); Liu, Enzuo, E-mail: ezliu@tju.edu.cn [School of Materials Science and Engineering and Tianjin Key Laboratory of Composites and Functional Materials, Tianjin University, Tianjin 300350 (China); Collaborative Innovation Center of Chemical Science and Engineering, Tianjin 300350 (China); He, Fang; Shi, Chunsheng [School of Materials Science and Engineering and Tianjin Key Laboratory of Composites and Functional Materials, Tianjin University, Tianjin 300350 (China); He, Chunnian [School of Materials Science and Engineering and Tianjin Key Laboratory of Composites and Functional Materials, Tianjin University, Tianjin 300350 (China); Collaborative Innovation Center of Chemical Science and Engineering, Tianjin 300350 (China); Li, Jiajun [School of Materials Science and Engineering and Tianjin Key Laboratory of Composites and Functional Materials, Tianjin University, Tianjin 300350 (China); Zhao, Naiqin, E-mail: nqzhao@tju.edu.cn [School of Materials Science and Engineering and Tianjin Key Laboratory of Composites and Functional Materials, Tianjin University, Tianjin 300350 (China); Collaborative Innovation Center of Chemical Science and Engineering, Tianjin 300350 (China)

2016-12-30

Highlights: • The 3D core-shell Fe{sub 2}O{sub 3}@C/CC structure is fabricated by simple hydrothermal route. • The composite connected 3D carbon networks consist of carbon cloth, Fe{sub 2}O{sub 3} nanorods and outer carbon layer. • The Fe{sub 2}O{sub 3}@C/CC used as binder-free anode in LIBs, demonstrates excellent performances. - Abstract: A facile and scalable strategy is developed to fabricate three dimensional core-shell Fe{sub 2}O{sub 3} @ carbon/carbon cloth structure by simple hydrothermal route as binder-free lithium-ion battery anode. In the unique structure, carbon coated Fe{sub 2}O{sub 3} nanorods uniformly disperse on carbon cloth which forms the conductive carbon network. The hierarchical porous Fe{sub 2}O{sub 3} nanorods in situ grown on the carbon cloth can effectively shorten the transfer paths of lithium ions and reduce the contact resistance. The carbon coating significantly inhibits pulverization of active materials during the repeated Li-ion insertion/extraction, as well as the direct exposure of Fe{sub 2}O{sub 3} to the electrolyte. Benefiting from the structural integrity and flexibility, the nanocomposites used as binder-free anode for lithium-ion batteries, demonstrate high reversible capacity and excellent cyclability. Moreover, this kind of material represents an alternative promising candidate for flexible, cost-effective, and binder-free energy storage devices.

Magnetic interaction reversal in watermelon nanostructured Cr-doped Fe nanoclusters

Energy Technology Data Exchange (ETDEWEB)

Kaur, Maninder; Qiang, You, E-mail: youqiang@uidaho.edu [Department of Physics, University of Idaho, Moscow, Idaho 83844 (United States); Dai, Qilin; Tang, Jinke [Department of Physics and Astronomy, University of Wyoming, Laramie, Wyoming 82071 (United States); Bowden, Mark; Engelhard, Mark [Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352 (United States); Wu, Yaqiao [Department of Materials Science and Engineering, Boise State University, Boise, Idaho 83725 (United States); Center for Advanced Energy Studies, Idaho Falls, Idaho 83401 (United States)

2013-11-11

Cr-doped core-shell Fe/Fe-oxide nanoclusters (NCs) were synthesized at varied atomic percentages of Cr from 0 at. % to 8 at. %. The low concentrations of Cr (<10 at. %) were selected in order to inhibit the complete conversion of the Fe-oxide shell to Cr{sub 2}O{sub 3} and the Fe core to FeCr alloy. The magnetic interaction in Fe/Fe-oxide NCs (∼25 nm) can be controlled by antiferromagnetic Cr-dopant. We report the origin of σ-FeCr phase at very low Cr concentration (2 at. %) unlike in previous studies, and the interaction reversal from dipolar to exchange interaction in watermelon-like Cr-doped core-shell NCs.

Magnetization-induced enhancement of photoluminescence in core-shell CoFe{sub 2}O{sub 4}@YVO{sub 4}:Eu{sup 3+} composite

Energy Technology Data Exchange (ETDEWEB)

Jia, Yanmin, E-mail: ymjia@zjnu.edu.cn, E-mail: wuzheng@zjnu.cn; Zhou, Zhihua; Wei, Yongbin [Department of Physics, Zhejiang Normal University, Jinhua 321004 (China); Wu, Zheng, E-mail: ymjia@zjnu.edu.cn, E-mail: wuzheng@zjnu.cn; Chen, Jianrong [College of Geography and Environmental Sciences, Zhejiang Normal University, Jinhua 321004 (China); Zhang, Yihe [School of Materials Science and Technology, China University of Geosciences, Beijing 100083 (China); Liu, Yongsheng [Department of Physics, Shanghai University of Electric Power, Shanghai 200090 (China)

2013-12-07

After the core-shell CoFe{sub 2}O{sub 4}@YVO{sub 4}:Eu{sup 3+} composite synthesized through a facile sol-gel method was magnetized under an external magnetic field of 0.25 T for 4 h, an enhancement of ∼56% in photoluminescence intensity was observed. The remanent magnetization of the CoFe{sub 2}O{sub 4} core increases the intensity of the excited charge transfer transition of VO{sub 4}{sup 3−} group in YVO{sub 4}:Eu{sup 3+} shell, which may enhance the probability related to the Eu{sup 3+} radiative transition {sup 5}D{sub 0}-{sup 7}F{sub 2}, yielding to a high photoluminescence. The obvious remanent-magnetization-induced enhancement in photoluminescence is helpful in developing excellent magnetic/luminescent material for the practical display devices.

Synthesis of bi-phase dispersible core-shell FeAu@ZnO magneto-opto-fluorescent nanoparticles

Science.gov (United States)

Li, Xue-Mei; Liu, Hong-Ling; Liu, Xiao; Fang, Ning; Wang, Xian-Hong; Wu, Jun-Hua

2015-11-01

Bi-phase dispersible core-shell FeAu@ZnO magneto-opto-fluorescent nanoparticles were synthesized by a modified nanoemulsion process using poly(ethylene glycol)-block-poly(propylene glycol)-block-poly(ethylene glycol) (PEO-PPO-PEO) as the surfactant. The morphology and crystal structure of the nanoparticles were studied by TEM/HRTEM and XRD. The nanoparticles manifest soft ferromagnetic and/or near superparamagnetic behavior with a small coercivity of ~19 Oe at room temperature. The corresponding magnetic hysteresis curves were elucidated by the modified Langevin equation. The FTIR study confirms the PEO-PPO-PEO molecules on the surface of the nanoparticles. The UV-vis and PL results reveal the well-behaved absorption bands including surface plasmon resonance and multiple visible fingerprint photoluminescent emissions of the nanoparticles dispersed in both hydrophilic and hydrophobic solvents. Moreover, the processes of solvent dispersion-collection of the nanoparticles were demonstrated for application readiness of such core-shell nanostructures.

Fe3O4@ZnO core-shell nanocomposites for efficient and repetitive removal of low density lipoprotein in plasma and on blood vessel

International Nuclear Information System (INIS)

Huang, Xiao; Lu, Juan; Yue, Danyang; Fan, Yijuan; Yi, Caixia; Wang, Xiaoying; Zhang, Mengxue; Pan, Jun

2015-01-01

Low density lipoprotein (LDL)-apheresis therapy, which directly removes LDL from plasma by LDL-adsorbents in vitro is found to be clinically effective and safe to lower the LDL content in blood to prevent cardiovascular disease. Thus, developing excellent LDL adsorbents are becoming more and more attractive. Herein, functional Fe 3 O 4 @ZnO core–shell nanocomposites have been synthesized by a facile and eco-friendly two-step method. Not only do they possess high LDL adsorption (in PBS/plasma as well as on blood vessels) and favorable magnetic targeting ability but they can also be reused conveniently, which offer the Fe 3 O 4 @ZnO core–shell nanocomposites significant potential in the removal of LDL in vitro and in vivo. (paper)

Influence of substrate treatment on the growth of advanced core–shell alloys and compounds of FeSi@SiO2 and SiO2 nanowires

CSIR Research Space (South Africa)

Thabethe, S

2014-12-01

Full Text Available Advanced core–shell FeSi@SiO(subx) nanowires are observed when FeCl(sub3) vapour is made to flow over a SiO(sub2)/Si substrate at 1100 degress C. The thickness of the SiO(subx) sheath (d0) is found to depend inversely as the period of time of HF...

Localized hole effects in inner-shell excitation

International Nuclear Information System (INIS)

Rescigno, T.N.; Orel, A.E.

1983-01-01

Ab initio calculations of valence shell ionization potentials have shown that orbital relaxation and correlation differences usually make contributions of comparable magnitude. In marked contrast to this observation is the situation for deep core ionization, where correlation differences (approx. 1 eV) play a relatively minor role compared to orbital relaxation (approx. 20 eV). Theoretical calculations have shown that this relaxation is most easily described if the 1s-vacancy created by a K-shell excitation is allowed to localize on one of the atomic centers. For molecules possessing a center of inversion, this means that the molecular orbitals that best describe the final state do not transform as any irreducible representation of the molecular point group. Recent experimental work by Shaw, King, Read and Cvejanovic and by Stefani and coworkers has prompted us to carry out further calculations on N 2 , as well as analogous investigations of 1s/sub N/ → π* excitation in NO and N 2 O. The generalized oscillator strengths display a striking similarity and point to the essential correctness of the localized hole picture for N 2 . The theoretical calculations are briefly described, followed by a summary of the results and comparison to experiment, followed by a short discussion

Wavelengths, classifications, and ionization energies in the isoelectronic sequences from Yb II and Yb III through Bi XV and Bi XVI

International Nuclear Information System (INIS)

Kaufman, V.; Sugar, J.

1976-01-01

Spectral observations are reported for transitions to the ground term and first excited term of the one-electron configurations in the 4f/sup 14/5p 6 nl isoelectronic sequence from Yb II through Bi XV. Resonance lines are reported for the isoelectronic sequence Yb III through Bi XVI in which the ground state is 4f/sup 14/5p 6 1 S 0 and the upper levels are the J = 1 levels of the 4f/sup 13/5p 6 nd, 4f/sup 14/5p 5 nd, and 4f/sup 14/5p 5 ns configurations. The wavelengths fall in the range 70--3700 A. The spectra were produced by means of sliding and triggered spark discharges and photographed with 10.7 m normal and grazing incidence spectrographs. The data in the Yb III sequence demonstrate the crossing of binding energies of the 4f and 5p shells at W VII. Rydberg series terms were found in a sufficient number of cases to provide extrapolation curves through Bi XV and Bi XVI. These data enabled us to calculate ionization energies for each of these ions with an uncertainty of approx.1% or better

Intershell correlations in photoionization of outer shells

Energy Technology Data Exchange (ETDEWEB)

Amusia, M.Ya. [The Racah Institute of Physics, The Hebrew University of Jerusalem, Jerusalem 91904 (Israel); A.F. Ioffe Physical-Technical Institute, St. Petersburg 194021 (Russian Federation); Chernysheva, L.V. [A.F. Ioffe Physical-Technical Institute, St. Petersburg 194021 (Russian Federation); Drukarev, E.G. [National Research Center “Kurchatov Institute”, Konstantinov Petersburg Nuclear Physics Institute, St. Petersburg 188300 (Russian Federation)

2016-02-15

We demonstrate that the cross sections for photoionization of the outer shells are noticeably modified at the photon energies close to the thresholds of ionization of the inner shells due to correlations with the latter. The correlations may lead to increase or to decrease of the cross sections just above the ionization thresholds.

Intershell correlations in photoionization of outer shells

International Nuclear Information System (INIS)

Amusia, M.Ya.; Chernysheva, L.V.; Drukarev, E.G.

2016-01-01

We demonstrate that the cross sections for photoionization of the outer shells are noticeably modified at the photon energies close to the thresholds of ionization of the inner shells due to correlations with the latter. The correlations may lead to increase or to decrease of the cross sections just above the ionization thresholds.

Compact Ag@Fe3O4 Core-shell Nanoparticles by Means of Single-step Thermal Decomposition Reaction

Science.gov (United States)

Brollo, Maria Eugênia F.; López-Ruiz, Román; Muraca, Diego; Figueroa, Santiago J. A.; Pirota, Kleber R.; Knobel, Marcelo

2014-10-01

A temperature pause introduced in a simple single-step thermal decomposition of iron, with the presence of silver seeds formed in the same reaction mixture, gives rise to novel compact heterostructures: brick-like Ag@Fe3O4 core-shell nanoparticles. This novel method is relatively easy to implement, and could contribute to overcome the challenge of obtaining a multifunctional heteroparticle in which a noble metal is surrounded by magnetite. Structural analyses of the samples show 4 nm silver nanoparticles wrapped within compact cubic external structures of Fe oxide, with curious rectangular shape. The magnetic properties indicate a near superparamagnetic like behavior with a weak hysteresis at room temperature. The value of the anisotropy involved makes these particles candidates to potential applications in nanomedicine.

A novel green synthesis of Fe{sub 3}O{sub 4}-Ag core shell recyclable nanoparticles using Vitis vinifera stem extract and its enhanced antibacterial performance

Energy Technology Data Exchange (ETDEWEB)

Venkateswarlu, Sada; Natesh Kumar, B.; Prathima, B. [Analytical and inorganic Division of Chemistry, S.V. University, Tirupati-517502, Andhra Pradesh (India); Anitha, K. [Department of Chemistry, S.K. University, Anantapur-515003, Andhra Pradesh (India); Jyothi, N.V.V., E-mail: nvvjyothi01@gmail.com [Analytical and inorganic Division of Chemistry, S.V. University, Tirupati-517502, Andhra Pradesh (India)

2015-01-15

We described a novel and eco-friendly method for preparing Fe{sub 3}O{sub 4}-Ag core shell nanoparticles (CSNPs) with high magnetism and potent antibacterial activity. The Fe{sub 3}O{sub 4}-Ag CSNPs were obtained using waste material of Vitis vinifera (grape) stem extract as the green solvent, reducing and capping agent. The result recorded from X-ray powder diffraction (XRD), UV–vis spectrum, energy dispersive spectroscopy (EDS), Fourier transform infrared spectroscopy (FT-IR) supports the biosynthesis and characterization of Fe{sub 3}O{sub 4}-Ag CSNPs. From transmission electron microscopy (TEM) the size of the Fe{sub 3}O{sub 4}-Ag nanoparticles was measured below 50 nm; high-resolution TEM (HRTEM) indicates the core shell structure; and selected area electron diffraction (SAED) has revealed polycrystalline nature. Vibrating sample magnetometer (VSM) shows the ferromagnetic nature of Fe{sub 3}O{sub 4}-Ag CSNPs at room temperature with saturation magnetization of 15.74 emu/g. Further, these biogenic nanoparticles were highly hazardous to microorganisms. The antibacterial activity of biogenic Fe{sub 3}O{sub 4}-Ag CSNPs showed potent inhibitory activity against both Gram-positive and Gram-negative pathogens. These nanoparticles may also be reusable because of its excellent ferromagnetic property.

Surface protection of inner shells of cooling towers. Positive long-term experience with coating systems.; Oberflaechenschutz von Kuehlturminnenschalen. Positive Langzeiterfahrungen mit Beschichtungssystemen

Energy Technology Data Exchange (ETDEWEB)

Heine, Peer [MC-Bauchemie Mueller GmbH und Co.KG, Bottrop (Germany)

2010-07-15

Natural-draught cooling tower are modern power plant components with great importance for safe and reliable power supply. Due to the complex effects of operating and environmental conditions especially on the inner shell, the concrete must be protected by special resin-based surface coating systems. Parallel to the development of the power plant technology, also the coating systems are under constant improvement in order to ensure reliable and permanent protection. The positive long-term experience suggests that power plant operators may rely on a high level of safety here. (orig.)

High-resolution K-shell spectra from laser excited molybdenum plasmas

Directory of Open Access Journals (Sweden)

Szabo C.I.

2013-11-01

Full Text Available X-ray spectra from Molybdenum plasmas were recorded by a Cauchois-type cylindrically bent Transmission Crystal Spectrometer (TCS. The absolutely calibrated spectrometer provides an unprecedented resolution of inner shell transitions (K x-ray radiation. This tool allows us to resolve individual lines from different charge states existing inside the laser-produced plasma. The inner shell transitions from highly charged Molybdenum shown in this report have never been resolved before in such detail in a laser-produced plasma.

Electrochemical synthesis of CORE-shell magnetic nanowires

KAUST Repository

Ovejero, Jesú s G.; Bran, Cristina; Vidal, Enrique Vilanova; Kosel, Jü rgen; Morales, Marí a P.; Vazquez, Manuel

2015-01-01

(Fe, Ni, CoFe) @ Au core-shell magnetic nanowires have been synthesized by optimized two-step potentiostatic electrodeposition inside self-assembled nanopores of anodic aluminium templates. The optimal electrochemical parameters (e.g., potential

Band-to-band and inner shell excitation VIS-UV photoluminescence of quaternary InAlGaN alloys

International Nuclear Information System (INIS)

Fukui, K.; Naoe, S.; Okada, K.; Hamada, S.; Hirayama, H.

2006-01-01

Visible and ultraviolet photoluminescence and photoluminescence excitation spectra of quaternary InAlGaN alloys were measured. The excitation photon energy covers from band edge to 180 eV, near both nitrogen K (∝400 eV) and aluminium K (∝1.5 keV) inner shell energy region. From photoluminescence excitation spectra photoluminescence intensity per incident photon number varies in proportion to incident photon energy. This result implies that many conduction band electron - valence band hole pairs which are responsible for photoluminescence are produced by high energy excitation. Time resolved decay curves were also measured in the same energy region. No effect of high energy excitation on time resolved decay measurements suggests a role of indium on the photoluminescence mechanism in InAlGaN system. (copyright 2006 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

Local hydrated structure of an Fe2+/Fe3+ aqueous solution: an investigation using a combination of molecular dynamics and X-ray absorption fine structure methods

International Nuclear Information System (INIS)

Ye Qing; Zhou Jing; Zhao Haifeng; Chen Xing; Chu Wangsheng; Zheng Xusheng; Marcelli, Augusto; Wu Ziyu

2013-01-01

The hydrated shell of both Fe 2+ and Fe 3+ aqueous solutions are investigated by using the molecular dynamics (MD) and X-ray absorption structure (XAS) methods. The MD simulations show that the first hydrated shells of both Fe 2+ and Fe 3+ are characterized by a regular octahedron with an Fe-O distance of 2.08Å for Fe 2+ and 1.96Å for Fe 3+ , and rule out the occurrence of a Jahn-Teller distortion in the hydrated shell of an Fe 2+ aqueous solution. The corresponding X-ray absorption near edge fine structure (XANES) calculation successfully reproduces all features in the XANES spectra in Fe 2+ and Fe 3+ aqueous solution. A feature that is located at energy 1 eV higher than the white line (WL) in an Fe 3+ aqueous solution may be assigned to the contribution of the charge transfer. (authors)

Composted oyster shell as lime fertilizer is more effective than fresh oyster shell.

Science.gov (United States)

Lee, Young Han; Islam, Shah Md Asraful; Hong, Sun Joo; Cho, Kye Man; Math, Renukaradhya K; Heo, Jae Young; Kim, Hoon; Yun, Han Dae

2010-01-01

Physio-chemical changes in oyster shell were examined, and fresh and composted oyster shell meals were compared as lime fertilizers in soybean cultivation. Structural changes in oyster shell were observed by AFM and FE-SEM. We found that grains of the oyster shell surface became smoother and smaller over time. FT-IR analysis indicated the degradation of a chitin-like compound of oyster shell. In chemical analysis, pH (12.3+/-0.24), electrical conductivity (4.1+/-0.24 dS m(-1)), and alkaline powder (53.3+/-1.12%) were highest in commercial lime. Besides, pH was higher in composted oyster shell meal (9.9+/-0.53) than in fresh oyster shell meal (8.4+/-0.32). The highest organic matter (1.1+/-0.08%), NaCl (0.54+/-0.03%), and moisture (15.1+/-1.95%) contents were found in fresh oyster shell meal. A significant higher yield of soybean (1.33 t ha(-1)) was obtained by applying composted oyster shell meal (a 21% higher yield than with fresh oyster shell meal). Thus composting of oyster shell increases the utility of oyster shell as a liming material for crop cultivation.

Reducing the effects of X-ray pre-heat in double shell NIF capsules by over-coating the high Z shell

Science.gov (United States)

Wilson, Douglas; Milovich, J. L.; Daughton, W. S.; Loomis, E. N.; Sauppe, J. P.; Dodd, E. S.; Merritt, E. C.; Montgomery, D. S.; Renner, D. B.; Haines, B. M.; Cardenas, T.; Desjardins, T.; Palaniyappan, S.; Batha, S. H.

2017-10-01

Hohlraum generated X-rays will penetrate the ablator of a double shell capsule and be absorbed in the outer surface of the inner capsule. The ablative pressure this generates drives a shock into the central fuel, and a reflected shock that reaches the inner high-Z shell surface before the main shock even enters the fuel. With a beryllium over-coat preheat X-rays deposit just inside the beryllium/high z interface. The beryllium tamps the preheat expansion, eliminating ablation, and dramatically reducing pressure. The slow shock or pressure wave it generates is then overtaken by the main shock, avoiding an early shock in the fuel and increasing capsule yield.

Highly selective and sensitive methanol gas sensor based on molecular imprinted silver-doped LaFeO3 core-shell and cage structures

Science.gov (United States)

Rong, Qian; Zhang, Yumin; Lv, Tianping; Shen, Kaiyuan; Zi, Baoye; Zhu, Zhongqi; Zhang, Jin; Liu, Qingju

2018-04-01

Silver-doped LaFeO3 molecularly imprinted polymers (SLMIPs) were synthesized by a sol-gel method combined with molecularly imprinted technology as precursors. The precursors were then used to prepare SLMIPs cage (SLM-cage) and SLMIPs core-shell (SLM-core-shell) structures by using a carbon sphere as the template and hydrothermal synthesis, respectively. The structures, morphologies, and surface areas of these materials were determined, as well as their gas-sensing properties and related mechanisms. The SLM-cage and SLM-core-shell samples exhibited good responses to methanol gas, with excellent selectivity. The response and optimum working temperature were 16.98 °C and 215 °C, 33.7 °C and 195 °C, respectively, with corresponding response and recovery times of 45 and 50 s (SLM-cage) and 42 and 57 s (SLM-core-shell) for 5 ppm methanol gas. Notably, the SLM-cage and SLM-core-shell samples exhibited lower responses (≤5 and ≤7, respectively) to other gases, including ethanol, ammonia, benzene, acetone, and toluene. Thus, these materials show potential as practical methanol detectors.

Hydrothermal synthesis of superparamagnetic and red luminescent bifunctional Fe{sub 3}O{sub 4}@Mn{sup 2+}-doped NaYF{sub 4}:Yb/Er core@shell monodisperse nanoparticles and their subsequent ligand exchange in water

Energy Technology Data Exchange (ETDEWEB)

Qin, Zhenli; Du, Sinan; Luo, Yang; Liao, Zhijian; Zuo, Fang, E-mail: polymerzf@swun.cn; Luo, Jianbin; Liu, Dong

2016-08-15

Graphical abstract: An efficient hydrothermal method was used to fabricate the superparamagnetic and red luminescent bifunctional Fe{sub 3}O{sub 4}@Mn{sup 2(*)+}-doped NaYF{sub 4}:Yb/Er nanoparticles (NPs) with core@shell structures through a seed-growth procedure. Then using PEG phosphate ligand to displace oleate from the as-synthesized NPs, hydrophilic Fe{sub 3}O{sub 4}@Mn{sup 2+}-doped NaYF{sub 4}:Yb/Er NPs with good water solubility are obtained. - Highlights: • Homogeneous size distribution of magnetic-upconversion core@shell structured nanoparticles (NPs) were synthesized. • The core@shell nanostructures were obtained by seed-growth method. • The oleic acid coated Fe{sub 3}O{sub 4} NPs were used as seeds and cores. • The magnetic-upconversion NPs emitted red luminescence under a 980 nm laser. • Synthesized magnetic-upconversion NPs were phase transferred using ligand exchange process. - Abstract: We report the use of an efficient hydrothermal method to synthesize superparamagnetic and red luminescent bifunctional Fe{sub 3}O{sub 4}@Mn{sup 2+}-doped NaYF{sub 4}:Yb/Er nanoparticles (NPs) with core@shell structures via a seed-growth procedure. Oleic acid coated Fe{sub 3}O{sub 4} (OA-Fe{sub 3}O{sub 4}) NPs were initially synthesized using a coprecipitation method. The as-synthesized OA-Fe{sub 3}O{sub 4} NPs were then used as seeds, on which the red upconversion luminescent shell (Mn{sup 2+}-doped NaYF{sub 4}:Yb/Er) was formed. Furthermore, hydrophobic to hydrophilic surface modification of the Fe{sub 3}O{sub 4}@Mn{sup 2+}-doped NaYF{sub 4}:Yb/Er NPs was achieved via a ligand exchange method where oleic acid was displaced by a PEG phosphate ligand [PEG = poly(ethylene glycol)]. These materials were characterized by means of transmission electron microscopy (TEM), X-ray diffraction (XRD), photoluminescence (PL) spectroscopy, and vibrating sample magnetometry (VSM). The Fe{sub 3}O{sub 4} cores were uniformly coated with a Mn{sup 2+}-doped NaYF{sub 4}:Yb

[Could phimosis have been the cause of sexual difficulties and delayed fertility of Louis XVI (1754-1793)?].

Science.gov (United States)

Androutsos, Georges

2002-02-01

The great majority of historians agree that the marriage of Louis XVI and Marie-Antoinette was only consumated seven years after the official ceremony. This delay could have been due to a genital malformation (phimosis) of Louis XVI, a strict religious education, a traumatic childhood and the young age of the two spouses, factors that may have inhibited their sexuality. In this article, the authors try to determine whether Louis XVI was able to overcome his sexual difficulties following an operation (circumcision) or as a result of spontaneous cure.

Core–shell Fe3O4–Au magnetic nanoparticles based nonenzymatic ultrasensitive electrochemiluminescence immunosensor using quantum dots functionalized graphene sheet as labels

International Nuclear Information System (INIS)

Liu, Weiyan; Zhang, Yan; Ge, Shenguang; Song, Xianrang; Huang, Jiadong; Yan, Mei; Yu, Jinghua

2013-01-01

Graphical abstract: Core–shell Fe 3 O 4 –Au magnetic nanoparticles and P-GS@QDs were prepared to immobilize Ab 1 and Ab 2 respectively and combined to fabricate a novel sandwich-type ECL immunosensor for detecting CA125 at low concentration. Highlights: ► ECL immunosensor for CA125 based on a microfluidic strategy with a homemade ECL cell was proposed. ► Core–shell Fe 3 O 4 –Au magnetic nanoparticles were employed as the carriers of the primary antibodies. ► CdTe quantum dots functionalized graphene sheet were used for signal amplification. -- Abstract: In this paper, a novel, low-cost electrochemiluminescence (ECL) immunosensor using core–shell Fe 3 O 4 –Au magnetic nanoparticles (AuMNPs) as the carriers of the primary antibody of carbohydrate antigen 125 (CA125) was designed. Graphene sheet (GS) with property of good conductivity and large surface area was a captivating candidate to amplify ECL signal. We successively synthesized functionalized GS by loading large amounts of quantum dots (QDs) onto the poly (diallyldimethyl-ammonium chloride) (PDDA) coated graphene sheet (P-GS@QDs) via self-assembly electrostatic reactions, which were used to label secondary antibodies. The ECL immunosensors coupled with a microfluidic strategy exhibited a wide detection range (0.005–50 U mL −1 ) and a low detection limit (1.2 mU mL −1 ) with the help of an external magnetic field to gather immunosensors. The method was evaluated with clinical serum sample, receiving good correlation with results from commercially available analytical procedure

Adsorption process of fluoride from drinking water with magnetic core-shell Ce-Ti@Fe3O4 and Ce-Ti oxide nanoparticles.

Science.gov (United States)

Abo Markeb, Ahmad; Alonso, Amanda; Sánchez, Antoni; Font, Xavier

2017-11-15

Synthesized magnetic core-shell Ce-Ti@Fe 3 O 4 nanoparticles were tested, as an adsorbent, for fluoride removal and the adsorption studies were optimized. Adsorption capacity was compared with the synthesized Ce-Ti oxide nanoparticles. The adsorption equilibrium for the Ce-Ti@Fe 3 O 4 adsorbent was found to occur in cycles of adsorption-desorption. Although the nanoparticles suffer slight structure modifications after their reusability, they keep their adsorption capacity. Likewise, the efficiency of the Ce-Ti@Fe 3 O 4 was demonstrated when applied to real water to obtain a residual concentration of F - below the maximum contaminated level, 1.5mg/L (WHO, 2006). Copyright © 2017 Elsevier B.V. All rights reserved.

Neutron transfer reactions in the fp-shell region

International Nuclear Information System (INIS)

Mahgoub, Mahmoud

2008-01-01

Neutron transfer reactions were used to study the stability of the magic number N=28 near 56 Ni. On one hand the one-neutron pickup (d,p) reaction was used for precision spectroscopy of single-particle levels in 55 Fe. On the other hand we investigated the two-neutron transfer mechanism into 56 Ni using the pickup reaction 58 Ni(vectorp,t) 56 Ni. In addition the reliability of inverse kinematics reactions at low energy to study exotic nuclei was tested by the neutron transfer reactions t( 40 Ar,p) 42 Ar and d( 54 Fe,p) 55 Fe using tritium and deuterium targets, respectively, and by comparing the results with those of the normal kinematics reactions. The experimental data, differential cross-section and analyzing powers, are compared to DWBA and coupled channel calculations utilizing the code CHUCK3. By performing the single-neutron stripping reaction (vectord,p) on 54 Fe the 1f 7/2 shell in the ground state configuration was found to be partly broken. The instability of the 1f 7/2 shell and the magic number N=28 was confirmed once by observing a number of levels with J π = 7/2 - at low excitation energies, which should not be populated if 54 Fe has a closed 1f 7/2 shell, and also by comparing our high precision experimental data with a large scale shell model calculation using the ANTOINE code [5]. Calculations including a partly broken 1f 7/2 shell show better agreement with the experiment. The instability of the 1f 7/2 shell was confirmed also by performing the two-neutron pick-up reaction (vectorp,t) on 58 Ni to study 56 Ni, where a considerable improvement in the DWBA calculation was observed after considering 1f 7/2 as a broken shell. To prove the reliability of inverse kinematics transfer reactions at low energies (∝ 2 AMeV), the aforementioned single-neutron transfer reaction (d,p) was repeated using a beam of 54 Fe ions and a deuteron target. From this inverse kinematics experiment we were able to reproduce the absolute cross-section and angular

Effect of perforation on the sound transmission through a double-walled cylindrical shell

Science.gov (United States)

Zhang, Qunlin; Mao, Yijun; Qi, Datong

2017-12-01

An analytical model is developed to study the sound transmission loss through a general double-walled cylindrical shell system with one or two walls perforated, which is excited by a plane wave in the presence of external mean flow. The shell motion is governed by the classical Donnell's thin shell theory, and the mean particle velocity model is employed to describe boundary conditions at interfaces between the shells and fluid media. In contrast to the conventional solid double-walled shell system, numerical results show that perforating the inner shell in the transmission side improves sound insulation performance over a wide frequency band, and removes fluctuation of sound transmission loss with frequency at mid-frequencies in the absence of external flow. Both the incidence and azimuthal angles have nearly negligible effect on the sound transmission loss over the low and middle frequency range when perforating the inner shell. Width of the frequency band with continuous sound transmission loss can be tuned by the perforation ratio.

The dorsal shell wall structure of Mesozoic ammonoids

Directory of Open Access Journals (Sweden)

Gregor Radtke

2017-03-01

Full Text Available The study of pristine preserved shells of Mesozoic Ammonoidea shows different types of construction and formation of the dorsal shell wall. We observe three major types: (i The vast majority of Ammonoidea, usually planispirally coiled, has a prismatic reduced dorsal shell wall which consists of an outer organic component (e.g., wrinkle layer, which is the first layer to be formed, and the subsequently formed dorsal inner prismatic layer. The dorsal mantle tissue suppresses the formation of the outer prismatic layer and nacreous layer. With the exception of the outer organic component, secretion of a shell wall is omitted at the aperture. A prismatic reduced dorsal shell wall is always secreted immediately after the hatching during early teleoconch formation. Due to its broad distribution in (planispiral Ammonoidea, the prismatic reduced dorsal shell wall is probably the general state. (ii Some planispirally coiled Ammonoidea have a nacreous reduced dorsal shell wall which consists of three mineralized layers: two prismatic layers (primary and secondary dorsal inner prismatic layer and an enclosed nacreous layer (secondary dorsal nacreous layer. The dorsal shell wall is omitted at the aperture and was secreted in the rear living chamber. Its layers are a continuation of an umbilical shell doubling (reinforcement by additional shell layers that extends towards the ventral crest of the preceding whorl. The nacreous reduced dorsal shell wall is formed in the process of ontogeny following a prismatic reduced dorsal shell wall. (iii Heteromorph and some planispirally coiled taxa secrete a complete dorsal shell wall which forms a continuation of the ventral and lateral shell layers. It is formed during ontogeny following a prismatic reduced dorsal shell wall or a priori. The construction is identical with the ventral and lateral shell wall, including a dorsal nacreous layer. The wide distribution of the ability to form dorsal nacre indicates that it is

Method of fabricating nested shells and resulting product

Science.gov (United States)

Henderson, Timothy M.; Kool, Lawrence B.

1982-01-01

A multiple shell structure and a method of manufacturing such structure wherein a hollow glass microsphere is surface treated in an organosilane solution so as to render the shell outer surface hydrophobic. The surface treated glass shell is then suspended in the oil phase of an oil-aqueous phase dispersion. The oil phase includes an organic film-forming monomer, a polymerization initiator and a blowing agent. A polymeric film forms at each phase boundary of the dispersion and is then expanded in a blowing operation so as to form an outer homogeneously integral monocellular substantially spherical thermoplastic shell encapsulating an inner glass shell of lesser diameter.

Isomeric island in the vicinity of 66Fe

International Nuclear Information System (INIS)

Daugas, J. M.; Belier, G.; Girod, M.; Goutte, H.; Meot, V.; Perru, O.; Roig, O.; Sauvestre, J. E.; Sawicka, M.; Pfuetzner, M.; Zylicz, J.; Matea, I.; Giovinazzo, J.; Grawe, H.; Becker, F.; Mayet, P.; Grzywacz, R.; Achouri, N. L.; Angelique, J. C.; Baiborodin, D.

2006-01-01

An island of isomers have recently been observed on both sides of the N=40 shell below the Ni isotopes. Isomeric states in the 65Fe and 67Fe allow the knowledge of the single particle structure around the νg9/2 shell. Moreover, the excitation energy of the first 2+ and 4+ states in the 68Fe have been established by β-γ correlation. The evolution of the structure of the Fe isotopes going far away from the valley of stability is, for the first time, given for N>40

Core-Shell Composite Fibers for High-Performance Flexible Supercapacitor Electrodes.

Science.gov (United States)

Lu, Xiaoyan; Shen, Chen; Zhang, Zeyang; Barrios, Elizabeth; Zhai, Lei

2018-01-31

Core-shell nanofibers containing poly(acrylic acid) (PAA) and manganese oxide nanoparticles as the core and polypyrrole (PPy) as the shell were fabricated through electrospinning the solution of PAA and manganese ions (PAA/Mn 2+ ). The obtained nanofibers were stabilized by Fe 3+ through the interaction between Fe 3+ ions and carboxylate groups. Subsequent oxidation of Mn 2+ by KMnO 4 produced uniform manganese dioxide (MnO 2 ) nanoparticles in the fibers. A PPy shell was created on the fibers by immersing the fibers in a pyrrole solution where the Fe 3+ ions in the fiber polymerized the pyrrole on the fiber surfaces. In the MnO 2 @PAA/PPy core-shell composite fibers, MnO 2 nanoparticles function as high-capacity materials, while the PPy shell prevents the loss of MnO 2 during the charge/discharge process. Such a unique structure makes the composite fibers efficient electrode materials for supercapacitors. The gravimetric specific capacity of the MnO 2 @PAA/PPy core-shell composite fibers was 564 F/g based on cyclic voltammetry curves at 10 mV/s and 580 F/g based on galvanostatic charge/discharge studies at 5 A/g. The MnO 2 @PAA/PPy core-shell composite fibers also present stable cycling performance with 100% capacitance retention after 5000 cycles.

Synthesis and electrochemical properties of Fe{sub 3}O{sub 4}@MOF core-shell microspheres as an anode for lithium ion battery application

Energy Technology Data Exchange (ETDEWEB)

Sun, Xuemin; Gao, Ge [Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry-of-Education Key Laboratory for Synthesis and Applications of Organic Functional Molecules, Hubei University, Wuhan 430062 (China); Yan, Dongwei, E-mail: dwyan@iccas.ac.cn [Advance Technology & Materials Co. Ltd., China Iron & Steel Research Institute Group, No. 76 Xueyuan Nanlu, Haidian District, Beijing 100081 (China); Feng, Chuanqi, E-mail: cfeng@hubu.edu.cn [Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry-of-Education Key Laboratory for Synthesis and Applications of Organic Functional Molecules, Hubei University, Wuhan 430062 (China)

2017-05-31

Highlights: • Fe{sub 3}O{sub 4} particles are encapsulated by HKUST-1 to form core-shell microspheres composite. • The composite exhibits outstanding electrochemical performances as a novel anode. • The typical approach can be used to prepare some novel electrode materials. - Abstract: The Fe{sub 3}O{sub 4}@MOF composite with a microspheric core and a porous metal-organic framework (MOF HKUST-1) shell has been successfully synthesized utilizing a versatile Layer-by-Layer (LBL) assembly method. The structure was identified by X-ray diffraction (XRD), and the morphology was investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques. The Fe{sub 3}O{sub 4}@MOF composite exhibited outstanding electrochemical properties when it was used as an anode material for lithium ion batteries (LIBs). After 100 discharge-charge cycles at a current density of 100 mA g{sup −1}, the reversible capacity of Fe{sub 3}O{sub 4}@MOF could maintain ∼1002 mAh g{sup −1}, which was much higher than that of the bare Fe{sub 3}O{sub 4} counterpart (696 mAh g{sup −1}). Moreover, load the current density as high as 2 A g{sup −1} (after 70 cycles at the current density step increased from 0.1 to 2 A g{sup −1}), it still delivered a reversible capacity of ∼429 mAh g{sup −1}. The results demonstrate that the cycling stability of Fe{sub 3}O{sub 4} as an anode could be significantly improved by coating Cu{sub 3}(1,3,5-benzenetricarboxylate){sub 2} (HKUST-1). This strategy may offer new route to prepare other composite materials using different particles and suitable Metal-organic frameworks (MOFs) for LIBs application.

THE ISLANDS PROJECT. I. ANDROMEDA XVI, AN EXTREMELY LOW MASS GALAXY NOT QUENCHED BY REIONIZATION

Energy Technology Data Exchange (ETDEWEB)

Monelli, Matteo; Martínez-Vázquez, Clara E.; Gallart, Carme; Hidalgo, Sebastian L.; Aparicio, Antonio [Instituto de Astrofísica de Canarias, La Laguna, Tenerife (Spain); Bernard, Edouard J. [Institute for Astronomy, University of Edinburgh, Royal Observatory, Blackford Hill, Edinburgh EH9 3HJ (United Kingdom); Skillman, Evan D.; McQuinn, Kristen B. W. [Minnesota Institute for Astrophysics, University of Minnesota, 116 Church Street, SE Minneapolis, MN, 55455 (United States); Weisz, Daniel R. [Astronomy Department, Box 351580, University of Washington, Seattle, WA, 98195 (United States); Dolphin, Andrew E. [Raytheon, 1151 E. Hermans Road, Tucson, AZ 85706 (United States); Cole, Andrew A. [School of Physical Sciences, University of Tasmania, Private Bag 37, Hobart 7005, TAS (Australia); Martin, Nicolas F. [Observatoire astronomique de Strasbourg, Universite de Strasbourg, CNRS, UMR 7550, 11 rue de l’Universite, F-67000 Strasbourg (France); Cassisi, Santi [INAF-Osservatorio Astronomico di Collurania, Teramo (Italy); Boylan-Kolchin, Michael [INAF–Osservatorio Astronomico di Teramo, via M. Maggini, 64100 Teramo (Italy); Mayer, Lucio [Department of Astronomy, The University of Texas at Austin, 2515 Speedway, Stop C1400, Austin, TX 78712 (United States); McConnachie, Alan [Herzberg Astronomy and Astrophysics, National Research Council Canada, 5071 West Saanich Road, Victoria, BC V9E 2E7 (Canada); Navarro, Julio F., E-mail: monelli@iac.es [Department of Physics and Astronomy, University of Victoria, P.O. Box 1700, STN CSC, Victoria, BC V8W 3P6 (Canada)

2016-03-10

Based on data aquired in 13 orbits of Hubble Space Telescope time, we present a detailed evolutionary history of the M31 dSph satellite Andromeda XVI, including its lifetime star formation history (SFH), the spatial distribution of its stellar populations, and the properties of its variable stars. And XVI is characterized by prolonged star formation activity from the oldest epochs until star formation was quenched ∼6 Gyr ago, and, notably, only half of the mass in stars of And XVI was in place 10 Gyr ago. And XVI appears to be a low-mass galaxy for which the early quenching by either reionization or starburst feedback seems highly unlikely, and thus it is most likely due to an environmental effect (e.g., an interaction), possibly connected to a late infall in the densest regions of the Local Group. Studying the SFH as a function of galactocentric radius, we detect a mild gradient in the SFH: the star formation activity between 6 and 8 Gyr ago is significantly stronger in the central regions than in the external regions, although the quenching age appears to be the same, within 1 Gyr. We also report the discovery of nine RR Lyrae (RRL) stars, eight of which belong to And XVI. The RRL stars allow a new estimate of the distance, (m − M){sub 0} = 23.72 ± 0.09 mag, which is marginally larger than previous estimates based on the tip of the red giant branch.

Magnetic interaction reversal in watermelon nanostructured Cr-doped Fe nanoclusters

International Nuclear Information System (INIS)

Kaur, Maninder; Qiang, You; Dai, Qilin; Tang, Jinke; Bowden, Mark; Engelhard, Mark; Wu, Yaqiao

2013-01-01

Cr-doped core-shell Fe/Fe-oxide nanoclusters (NCs) were synthesized at varied atomic percentages of Cr from 0 at. % to 8 at. %. The low concentrations of Cr ( 2 O 3 and the Fe core to FeCr alloy. The magnetic interaction in Fe/Fe-oxide NCs (∼25 nm) can be controlled by antiferromagnetic Cr-dopant. We report the origin of σ-FeCr phase at very low Cr concentration (2 at. %) unlike in previous studies, and the interaction reversal from dipolar to exchange interaction in watermelon-like Cr-doped core-shell NCs

Structure and dynamics of hydrated Fe(II) and Fe(III) ions. Quantum mechanical and molecular mechanical simulations

International Nuclear Information System (INIS)

Remsungnen, T.

2002-11-01

Classical molecular dynamics (MD) and combined em ab initio quantum mechanical/molecular mechanical molecular dynamics (QM/MM-MD) simulations have been performed to investigate structural, dynamical and energetical properties of Fe(II), and Fe(III) transition metal ions in aqueous solution. In the QM/MM-MD simulations the ion and its first hydration sphere were treated at the Hartree-Fock ab initio quantum mechanical level, while ab initio generated pair plus three-body potentials were employed for the remaining system. For the classical MD simulation the pair plus three-body potential were employed for all ion-water interactions. The coordination number of the first hydration shell is 100 % of 6 in both cases. The number of waters in the second hydration shell obtained from classical simulations are 13.4 and 15.1 for Fe(II) and Fe(III), respectively, while QM/MM-MD gives the values of 12.4 and 13.4 for Fe(II) and Fe(III). The energies of hydration obtained from MD and QM/MM-MD for Fe(II) are 520 and 500 kcal/mol, and for Fe(III) 1160 and 1100 kcal/mol respectively. The mean residence times of water in the second shell obtained from QM/MM-MD are 24 and 48 ps for Fe(II) and Fe(III), respectively. In contrast to the data obtained from classical MD simulation, the QM/MM-MD values are all in good agreement with the experimental data available. These investigations and results clearly indicate that many-body effects are essential for the proper description of all properties of the aqueous solution of both Fe(II) and Fe(III) ions. (author)

Hierarchical 3D NiFe2O4@MnO2 core-shell nanosheet arrays on Ni foam for high-performance asymmetric supercapacitors.

Science.gov (United States)

Zhang, Xinyang; Zhang, Ziqing; Sun, Shuanggan; Sun, Qiushi; Liu, Xiaoyang

2018-02-13

Hierarchical NiFe 2 O 4 @MnO 2 core-shell nanosheet arrays (NSAs) were synthesized on Ni foam as an integrated electrode for supercapacitors, using a facile two-step hydrothermal method followed by calcination treatment. The NiFe 2 O 4 nanosheets were designed as the core and ultrathin MnO 2 nanoflakes as the shell, creating a unique three-dimensional (3D) hierarchical electrode on Ni foam. The composite electrode exhibited remarkable electrochemical performance with a high specific capacitance of 1391 F g -1 at a current density of 2 mA cm -2 and long cycling stability at a high current density of 10 mA cm -2 (only 11.4% loss after 3000 cycles). Additionally, an asymmetric supercapacitor (ASC) device was fabricated with a NiFe 2 O 4 @MnO 2 composite as the positive electrode material and activated carbon (AC) as the negative one. The ASC device exhibited a high energy density (45.2 W h kg -1 ) at a power density of 174 W kg -1 , and an excellent cycling stability over 3000 cycles with 92.5% capacitance retention. The remarkable electrochemical performance demonstrated its great potential as a promising candidate for high-performance supercapacitors.

Neutron transfer reactions in the fp-shell region

Energy Technology Data Exchange (ETDEWEB)

Mahgoub, Mahmoud

2008-06-26

Neutron transfer reactions were used to study the stability of the magic number N=28 near {sup 56}Ni. On one hand the one-neutron pickup (d,p) reaction was used for precision spectroscopy of single-particle levels in {sup 55}Fe. On the other hand we investigated the two-neutron transfer mechanism into {sup 56}Ni using the pickup reaction {sup 58}Ni((vector)p,t){sup 56}Ni. In addition the reliability of inverse kinematics reactions at low energy to study exotic nuclei was tested by the neutron transfer reactions t({sup 40}Ar,p){sup 42}Ar and d({sup 54}Fe,p){sup 55}Fe using tritium and deuterium targets, respectively, and by comparing the results with those of the normal kinematics reactions. The experimental data, differential cross-section and analyzing powers, are compared to DWBA and coupled channel calculations utilizing the code CHUCK3. By performing the single-neutron stripping reaction ((vector)d,p) on {sup 54}Fe the 1f{sub 7/2} shell in the ground state configuration was found to be partly broken. The instability of the 1f{sub 7/2} shell and the magic number N=28 was confirmed once by observing a number of levels with J{sup {pi}} = 7/2{sup -} at low excitation energies, which should not be populated if {sup 54}Fe has a closed 1f{sub 7/2} shell, and also by comparing our high precision experimental data with a large scale shell model calculation using the ANTOINE code [5]. Calculations including a partly broken 1f{sub 7/2} shell show better agreement with the experiment. The instability of the 1f{sub 7/2} shell was confirmed also by performing the two-neutron pick-up reaction ((vector)p,t) on {sup 58}Ni to study {sup 56}Ni, where a considerable improvement in the DWBA calculation was observed after considering 1f{sub 7/2} as a broken shell. To prove the reliability of inverse kinematics transfer reactions at low energies ({proportional_to} 2 AMeV), the aforementioned single-neutron transfer reaction (d,p) was repeated using a beam of {sup 54}Fe ions and a

Inner-Shell Excitations of 2p Electrons of Argon Investigated by Fast Electron Impact with High Resolution

International Nuclear Information System (INIS)

Ren Lin-Mao; Wang You-Yan; Li Dong-Dong; Yuan Zhen-Sheng; Zhu Lin-Fan

2011-01-01

Electron energy loss spectra of inner-shell excitations of 2p electrons of argon are measured at an incident electron energy of 2500 eV and scattering angles of 0° and 4°. The dipole-forbidden transitions of 2p −1 3/2 4p and 2p −1 3/2 5p are observed in the measured spectra and assigned based on the calculations of the Cowan code. The positions and line widths for the excitations of 2p −1 3/2 nl and 2p −1 1/2 nl (n ≤ 5) of argon are determined. The present results show that the line widths of the electric quadrupole transitions of 2p −1 3/2 4p[5/2 + 3/2] 2 and the electric monopole one of 2p −1 3/2 4p[1/2] 0 are less than those of the dipole-allowed transitions. (atomic and molecular physics)

Switchable transport strategy to deposit active Fe/Fe3C cores into hollow microporous carbons for efficient chromium removal.

Science.gov (United States)

Liu, Dong-Hai; Guo, Yue; Zhang, Lu-Hua; Li, Wen-Cui; Sun, Tao; Lu, An-Hui

2013-11-25

Magnetic hollow structures with microporous shell and highly dispersed active cores (Fe/Fe3 C nanoparticles) are rationally designed and fabricated by solution-phase switchable transport of active iron species combined with a solid-state thermolysis technique, thus allowing selective encapsulation of functional Fe/Fe3 C nanoparticles in the interior cavity. These engineered functional materials show high loading (≈54 wt%) of Fe, excellent chromium removal capability (100 mg g(-1)), fast adsorption rate (8766 mL mg(-1) h(-1)), and easy magnetic separation property (63.25 emu g(-1)). During the adsorption process, the internal highly dispersed Fe/Fe3 C nanoparticles supply a driving force for facilitating Cr(VI) diffusion inward, thus improving the adsorption rate and the adsorption capacity. At the same time, the external microporous carbon shell can also efficiently trap guest Cr(VI) ions and protect Fe/Fe3 C nanoparticles from corrosion and subsequent leaching problems. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Optimal design of hollow core–shell structural active materials for lithium ion batteries

Directory of Open Access Journals (Sweden)

Wenjuan Jiang

2015-01-01

Full Text Available To mitigate mechanical and chemical degradation of active materials, hollow core–shell structures have been applied in lithium ion batteries. Without embedding of lithium ions, the rigid coating shell can constrain the inward volume deformation. In this paper, optimal conditions for the full use of inner hollow space are identified in terms of the critical ratio of shell thickness and inner size and the state of charge. It is shown that the critical ratios are 0.10 and 0.15 for Si particle and tube (0.12 and 0.18 for Sn particle and tube, and above which there is lack of space for further lithiation.

Reduced Magnetism in Core–Shell Magnetite@MOF Composites

Energy Technology Data Exchange (ETDEWEB)

Elsaidi, Sameh K.; Sinnwell, Michael A.; Banerjee, Debasis; Devaraj, Arun; Kukkadapu, Ravi K.; Droubay, Timothy C.; Nie, Zimin; Kovarik, Libor; Murugesan, Vijayakumar; Manandhar, Sandeep; Nandasiri, Manjula I.; McGrail, Bernard P.; Thallapally, Praveen K.

2017-10-17

Rare-earth elements (REEs) have significant commercial and military uses.1-3 However, REE extraction through conventional mining processes is expensive and feasible at only a few locations worldwide. Alternative methods are needed to produce REEs from more geographically disperse resources and in a cost effective, environmental friendly manner.4,5 Among various sources, geothermal brine, used for generating geothermal energy can possess attractive concentrations (ppb to ppm level) of REEs along with other dissolved metal ions.6 A system that can selectively trap the REEs using an existing geothermal power plant infrastructure would be an attractive additional revenue stream for the plant operator that could accelerate the development and deployment of geothermal plants in the United States and rest of the world.7,8 Here, we demonstrate a magnetic core-shell approach that can effectively extract REEs in their ionic form from aqueous solution with up to 99.99% removal efficiency. The shell, composed of thermally and chemically stable functionalized metal-organic framework (MOF), is grown over a synthesized Fe3O4 magnetic core. Magnetic susceptibility of the particles was found to decline significantly after in situ growth of a MOF shell, which resulted from oxidation of Fe2+ species of the magnetite (Fe3O4) to Fe3+ species (maghemite). The core-shell particles can be completely removed from the mixture under an applied magnetic field, offering a practical, economic, and efficient REE-removal process.

Core-shell iron-iron oxide nanoparticles

DEFF Research Database (Denmark)

Kuhn, Luise Theil; Bojesen, A.; Timmermann, L.

2004-01-01

We present studies of the magnetic properties of core-shell iron-iron oxide nanoparticles. By combining Mossbauer and X-ray absorption spectroscopy we have been able to measure the change from a Fe3O4-like to a gamma-Fe2O3-like composition from the interface to the surface. Furthermore, we have...

Synthesis and magnetic properties of cobalt-iron/cobalt-ferrite soft/hard magnetic core/shell nanowires

Science.gov (United States)

Leandro Londoño-Calderón, César; Moscoso-Londoño, Oscar; Muraca, Diego; Arzuza, Luis; Carvalho, Peterson; Pirota, Kleber Roberto; Knobel, Marcelo; Pampillo, Laura Gabriela; Martínez-García, Ricardo

2017-06-01

A straightforward method for the synthesis of CoFe2.7/CoFe2O4 core/shell nanowires is described. The proposed method starts with a conventional pulsed electrodeposition procedure on alumina nanoporous template. The obtained CoFe2.7 nanowires are released from the template and allowed to oxidize at room conditions over several weeks. The effects of partial oxidation on the structural and magnetic properties were studied by x-ray spectrometry, magnetometry, and scanning and transmission electron microscopy. The results indicate that the final nanowires are composed of 5 nm iron-cobalt alloy nanoparticles. Releasing the nanowires at room conditions promoted surface oxidation of the nanoparticles and created a CoFe2O4 shell spinel-like structure. The shell avoids internal oxidation and promotes the formation of bi-magnetic soft/hard magnetic core/shell nanowires. The magnetic properties of both the initial single-phase CoFe2.7 nanowires and the final core/shell nanowires, reveal that the changes in the properties from the array are due to the oxidation more than effects associated with released processes (disorder and agglomeration).

A new insight on the core–shell structure of zerovalent iron nanoparticles and its application for Pb(II) sequestration

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yalei, E-mail: zhangyalei@tongji.edu.cn [State Key Laboratory of Pollution Control and Resources Reuse, Tongji University, Shanghai 200092 (China); Key Laboratory of Yangtze Water Environment for Ministry of Education, Tongji University, Shanghai 200092 (China); Su, Yiming [State Key Laboratory of Pollution Control and Resources Reuse, Tongji University, Shanghai 200092 (China); Zhou, Xuefei, E-mail: zhouxuefei@tongji.edu.cn [State Key Laboratory of Pollution Control and Resources Reuse, Tongji University, Shanghai 200092 (China); Dai, Chaomeng [State Key Laboratory of Pollution Control and Resources Reuse, Tongji University, Shanghai 200092 (China); College of Civil Engineering, Tongji University, Shanghai 200092 (China); Keller, Arturo A. [Bren School of Environmental Science and Management, University of California, Santa Barbara (United States)

2013-12-15

Highlights: • The shell of nZVI is composed of 45.5% Fe(OH){sub 3} and 54.5% FeOOH. • Fe(OH){sub 3} shell suppresses the reduction of Pb(II). • Fe(OH){sub 3} shell greatly promotes the co-precipitation and adsorption of Pb(II). • pH < 4.5 favors Fe dissolution, while pH > 4.5 promotes Pb(II) adsorption. • A reaction between Fe{sup 0} core, Fe(OH){sub 3} and Pb(II) is proposed. -- Abstract: Nanoscale zerovalent iron (nZVI) has shown a high efficacy for removing heavy metals from liquid solution. However, its removal capacity has not been fully explored due to its common shell composition (FeOOH). In this study, a much higher removal capacity of Pb(II) is observed (1667 mg Pb(II)/g Fe), which is over 100% higher than the highest removal capacity of nZVI reported before. High-resolution X-ray photoelectron spectroscopy (HR-XPS) reveals that through restricting the dehydration process of Fe(OH){sub 3}, nZVI can acquire a unique shell, which is composed of 45.5% Fe(OH){sub 3} and 54.5% FeOOH. The presence of Fe(OH){sub 3} suppresses the reduction of Pb(II), but greatly promotes the co-precipitation and adsorption of Pb(II). Combining the ratio of Fe-released to Pb-immobilized and the result of HR-XPS, a reaction between Fe{sup 0} core, Fe(OH){sub 3}, and Pb(II) is proposed. The Fe released from the Fe{sup 0} core leads to the core depletion, observed by transmission electron microscopy (TEM) under high Pb(II) loading. While temperature has little influence on the removal capacity, pH affects the removal capacity greatly. pH < 4.5 favors Fe dissolution, while pH > 4.5 promotes Pb(II) adsorption. Given the high Pb removal capacity via the Fe(OH){sub 3} shell, nZVI can be used to remedy Pb(II) contamination.

Thermodynamical Properties of 56Fe

International Nuclear Information System (INIS)

Tavukcu, E.; Becker, J.A.; Bernstein, L.A.; Garrett, P.E.; Guttormsen, M.; Mitchell, G.E.; Rekstad, J.; Schiller, A.; Siem, S.; Voinov, A.; Younes, W.

2002-01-01

Average nuclear level densities close to the nuclear binding energy in 56 Fe and 57 Fe are extracted from primary γ-ray spectra. Thermal properties of 56 Fe are studied within the statistical canonical ensemble. The experimental heat capacity is compared with the theoretical heat capacity calculated within the shell model Monte Carlo approach

Inner-shell ionization of heavy atoms by slow ions. A study of electronic relativistic effects and projectile Coulomb deflection in the Semiclassical Approximation

International Nuclear Information System (INIS)

Amundsen, P.A.

1978-08-01

Several investigations have been made on K and L shell ionization of the heavy collision partner in slow asymmetric collisions based on the SCA. The use of the SCA can only be defended for slow collisions if the projectile has a charge much less than the target. Thus this approximation should first be tested for proton impact on very heavy target elements. For these elements the inner shell electrons move sufficiently fast for a relativistic description to be mandatory. These relativistic effects are in themselves of some interest, as they can be quite large. After discussion of the formulation of the SCA used throughout this work, a further introduction is given on relativistic effects in Coulomb ionisation. Two papers on electronic relativistic effects in K and L shell ionization follow. The next two papers discuss calculations with an exact Coulomb projectile path. The latter of these also touches upon the inclusion of corrections to the SCA from terms beyond first order perturbation theory. In the last paper of this thesis it is shown how the theoretical apparatus developed for the SCA- calculations can immediately be used also for making calculations of more symmetric systems with the Briggs model. Thus, at least for direct ionization in very slow collisions a unification of the SA and MO approaches has apparently been reached. (JIW)

Comparing M31 and Milky Way satellites: The extended star formation histories of Andromeda II and Andromeda XVI

Energy Technology Data Exchange (ETDEWEB)

Weisz, Daniel R. [Department of Astronomy, University of California at Santa Cruz, 1156 High Street, Santa Cruz, CA 95064 (United States); Skillman, Evan D.; McQuinn, Kristen B. W. [Minnesota Institute for Astrophysics, University of Minnesota, Minneapolis, MN (United States); Hidalgo, Sebastian L.; Monelli, Matteo; Gallart, Carme; Aparicio, Antonio [Instituto de Astrofísica de Canarias. Vía Láctea s/n., E-38200 La Laguna, Tenerife, Canary Islands (Spain); Dolphin, Andrew E. [Raytheon, 1151 E. Hermans Road, Tucson, AZ 85706 (United States); McConnachie, Alan; Stetson, Peter B. [Dominion Astrophysical Observatory, Herzberg Institute of Astrophysics, National Research Council, 5071 West Saanich Road, Victoria, BC V9E 2E7 (Canada); Bernard, Edouard J. [Institute for Astronomy, University of Edinburgh, Royal Observatory, Blackford Hill, Edinburgh EH9 3HJ (United Kingdom); Boylan-Kolchin, Michael [Astronomy Department, University of Maryland, College Park, MD (United States); Cassisi, Santi [INAF-Osservatorio Astronomico di Collurania, Teramo (Italy); Cole, Andrew A. [School of Mathematics and Physics, University of Tasmania, Hobart, Tasmania (Australia); Ferguson, Henry C. [Space Telescope Science Institute, 3700 San Martin Drive, Baltimore, MD 21218 (United States); Irwin, Mike [Institute of Astronomy, University of Cambridge, Madingley Road, Cambridge CB3 0HA (United Kingdom); Martin, Nicolas F. [Observatoire astronomique de Strasbourg, Universit de Strasbourg, CNRS, UMR 7550, 11 rue de l' Universit, F-67000 Strasbourg (France); Mayer, Lucio [Institut für Theoretische Physik, University of Zurich, Zürich (Switzerland); Navarro, Julio F., E-mail: drw@ucsc.edu [Department of Physics and Astronomy, University of Victoria, BC V8P 5C2 (Canada)

2014-07-01

We present the first comparison between the lifetime star formation histories (SFHs) of M31 and Milky Way (MW) satellites. Using the Advanced Camera for Surveys on board the Hubble Space Telescope, we obtained deep optical imaging of Andromeda II (And II; M{sub V} = –12.0; log(M {sub *}/M {sub ☉}) ∼ 6.7) and Andromeda XVI (And XVI; M{sub V} = –7.5; log(M {sub *}/M {sub ☉}) ∼ 4.9) yielding color-magnitude diagrams that extend at least 1 mag below the oldest main-sequence turnoff, and are similar in quality to those available for the MW companions. And II and And XVI show strikingly similar SFHs: both formed 50%-70% of their total stellar mass between 12.5 and 5 Gyr ago (z ∼ 5-0.5) and both were abruptly quenched ∼5 Gyr ago (z ∼ 0.5). The predominance of intermediate age populations in And XVI makes it qualitatively different from faint companions of the MW and clearly not a pre-reionization fossil. Neither And II nor And XVI appears to have a clear analog among MW companions, and the degree of similarity in the SFHs of And II and And XVI is not seen among comparably faint-luminous pairs of MW satellites. These findings provide hints that satellite galaxy evolution may vary substantially among hosts of similar stellar mass. Although comparably deep observations of more M31 satellites are needed to further explore this hypothesis, our results underline the need for caution when interpreting satellite galaxies of an individual system in a broader cosmological context.

Bending stresses in Facetted Glass Shells

DEFF Research Database (Denmark)

Bagger, Anne; Jönsson, Jeppe; Almegaard, Henrik

2008-01-01

A shell structure of glass combines a highly effective structural principle with a material of optimal permeability to light. A facetted shell structure has a piecewise plane geometry, and together the facets form an approximation to a curved surface. A distributed load on a plane-based facetted...... structure will locally cause bending moments in the loaded facets. The bending stresses are dependent on the stiffness of the joints. Approximate solutions are developed to estimate the magnitude of the bending stresses. A FE-model of a facetted glass shell structure is used to validate the expressions...

Proteomics and the Inner Ear

Directory of Open Access Journals (Sweden)

Isolde Thalmann

2001-01-01

Full Text Available The inner ear, one of the most complex organs, contains within its bony shell three sensory systems, the evolutionary oldest gravity receptor system, the three semicircular canals for the detection of angular acceleration, and the auditory system - unrivaled in sensitivity and frequency discrimination. All three systems are susceptible to a host of afflictions affecting the quality of life for all of us. In the first part of this review we present an introduction to the milestones of inner ear research to pave the way for understanding the complexities of a proteomics approach to the ear. Minute sensory structures, surrounded by large fluid spaces and a hard bony shell, pose extreme challenges to the ear researcher. In spite of these obstacles, a powerful preparatory technique was developed, whereby precisely defined microscopic tissue elements can be isolated and analyzed, while maintaining the biochemical state representative of the in vivo conditions. The second part consists of a discussion of proteomics as a tool in the elucidation of basic and pathologic mechanisms, diagnosis of disease, as well as treatment. Examples are the organ of Corti proteins OCP1 and OCP2, oncomodulin, a highly specific calcium-binding protein, and several disease entities, Meniere's disease, benign paroxysmal positional vertigo, and perilymphatic fistula.

Continuous flame aerosol synthesis of carbon-coated nano-LiFePO4 for Li-ion batteries

Science.gov (United States)

Waser, Oliver; Büchel, Robert; Hintennach, Andreas; Novák, Petr; Pratsinis, Sotiris E.

2013-01-01

Core-shell, nanosized LiFePO4-carbon particles were made in one step by scalable flame aerosol technology at 7 g/h. Core LiFePO4 particles were made in an enclosed flame spray pyrolysis (FSP) unit and were coated in-situ downstream by auto thermal carbonization (pyrolysis) of swirl-fed C2H2 in an O2-controlled atmosphere. The formation of acetylene carbon black (ACB) shell was investigated as a function of the process fuel-oxidant equivalence ratio (EQR). The core-shell morphology was obtained at slightly fuel-rich conditions (1.0 < EQR < 1.07) whereas segregated ACB and LiFePO4 particles were formed at fuel-lean conditions (0.8 < EQR < 1). Post-annealing of core-shell particles in reducing environment (5 vol% H2 in argon) at 700 °C for up to 4 hours established phase pure, monocrystalline LiFePO4 with a crystal size of 65 nm and 30 wt% ACB content. Uncoated LiFePO4 or segregated LiFePO4-ACB grew to 250 nm at these conditions. Annealing at 800 °C induced carbothermal reduction of LiFePO4 to Fe2P by ACB shell consumption that resulted in cavities between carbon shell and core LiFePO4 and even slight LiFePO4 crystal growth but better electrochemical performance. The present carbon-coated LiFePO4 showed superior cycle stability and higher rate capability than the benchmark, commercially available LiFePO4. PMID:23407817

A TEMPORAL MAP IN GEOSTATIONARY ORBIT: THE COVER ETCHING ON THE EchoStar XVI ARTIFACT

Energy Technology Data Exchange (ETDEWEB)

Weisberg, Joel M., E-mail: jweisber@carleton.edu [Department of Physics and Astronomy, Carleton College, Northfield, MN 55057 (United States); Paglen, Trevor, E-mail: trevor@paglen.com

2012-10-01

Geostationary satellites are unique among orbital spacecraft in that they experience no appreciable atmospheric drag. After concluding their respective missions, geostationary spacecraft remain in orbit virtually in perpetuity. As such, they represent some of human civilization's longest lasting artifacts. With this in mind, the EchoStar XVI satellite, to be launched in fall 2012, will play host to a time capsule intended as a message for the deep future. Inspired in part by the Pioneer Plaque and Voyager Golden Records, the EchoStar XVI Artifact is a pair of gold-plated aluminum jackets housing a small silicon disk containing 100 photographs. The Cover Etching, the subject of this paper, is etched onto one of the two jackets. It is a temporal map consisting of a star chart, pulsar timings, and other information describing the epoch from which EchoStar XVI came. The pulsar sample consists of 13 rapidly rotating objects, 5 of which are especially stable, having spin periods <10 ms and extremely small spin-down rates. In this paper, we discuss our approach to the time map etched onto the cover and the scientific data shown on it, and we speculate on the uses that future scientists may have for its data. The other portions of the EchoStar XVI Artifact will be discussed elsewhere.

A TEMPORAL MAP IN GEOSTATIONARY ORBIT: THE COVER ETCHING ON THE EchoStar XVI ARTIFACT

International Nuclear Information System (INIS)

Weisberg, Joel M.; Paglen, Trevor

2012-01-01

Geostationary satellites are unique among orbital spacecraft in that they experience no appreciable atmospheric drag. After concluding their respective missions, geostationary spacecraft remain in orbit virtually in perpetuity. As such, they represent some of human civilization's longest lasting artifacts. With this in mind, the EchoStar XVI satellite, to be launched in fall 2012, will play host to a time capsule intended as a message for the deep future. Inspired in part by the Pioneer Plaque and Voyager Golden Records, the EchoStar XVI Artifact is a pair of gold-plated aluminum jackets housing a small silicon disk containing 100 photographs. The Cover Etching, the subject of this paper, is etched onto one of the two jackets. It is a temporal map consisting of a star chart, pulsar timings, and other information describing the epoch from which EchoStar XVI came. The pulsar sample consists of 13 rapidly rotating objects, 5 of which are especially stable, having spin periods <10 ms and extremely small spin-down rates. In this paper, we discuss our approach to the time map etched onto the cover and the scientific data shown on it, and we speculate on the uses that future scientists may have for its data. The other portions of the EchoStar XVI Artifact will be discussed elsewhere.

Mussel shell evaluation as bioindicator for heavy metals

Energy Technology Data Exchange (ETDEWEB)

Andrello, Avacir Casanova; Lopes, Fabio; Galvao, Tiago D. [Universidade Estadual de Londrina (UEL), PR (Brazil). Dept. de Fisica. Lab. de Fisica Nuclear Aplicada

2009-07-01

Full text: Recently, in Brazil, it has been appearing a new and unusual 'plague' in leisure and commercial fishing, caused by the parasitic larval phase of certain native bivalve mollusks of fresh water known as 'Naiades'. Such situation involves the presence of big bivalve of fresh water, mainly Anodontites trapesialis, in the tanks and dams of the fish creation, such bivalve mollusks belonging to the Ordem Unionoida and the Familia Mycetopodidae. The present work objectified to analyze the shells of such mollusks to verify the possibility of such mollusks as bioindicators of heavy metals in fresh water. The mollusks shells were collected in a commercial fishing at Londrina-PR, and analyzed qualitatively to determine the chemical composition and possible correlation with existent heavy metals in the aquatic environment. Studies of the literature have been showing that those mollusks are susceptible the existent chemical alterations in the aquatic environment due to anthropogenic action. Three different shells were analyzed, with the measures done on the external and internal side, using a portable Energy Dispersive X-Ray Fluorescence system (PXRF-LFNA-02). The measures were realized in the applied nuclear physics laboratory of State University of Londrina, and the PXRF-LFNA-02 is composed by a X-Ray tube (with Ag target and filter) with potency of 4W, and a detector Si-PIN model XR-100CR of Ampetc Inc. with resolution of 221eV for the line of 5.9 keV of the {sup 55}Fe (with a 25{mu}m Be window thickness and Ag collimator), Current 10 mA and High Voltage 28 kV. In the internal part of shells were identified the elements Ca, P, Fe, Mn and Sr and in the external part were identified Ca, P, Fe, Mn, Sr and Cu. The Ca ratio among the external and internal sides of the analyzed shells is around of 1, and it was expected because Ca is the main composed of mollusks shells. The ratio of P, Fe, Mn, and Sr for Ca stayed constant in all analyzed shells

Synthesis of core-shell hematite (α-Fe2O3) nanoplates: Quantitative analysis of the particle structure and shape, high coercivity and low cytotoxicity

Science.gov (United States)

Tadic, Marin; Kopanja, Lazar; Panjan, Matjaz; Kralj, Slavko; Nikodinovic-Runic, Jasmina; Stojanovic, Zoran

2017-05-01

Hematite core-shell nanoparticles with plate-like morphology were synthesized using a one-step hydrothermal synthesis. An XRPD analysis indicates that the sample consist of single-phase α-Fe2O3 nanoparticles. SEM and TEM measurements show that the hematite sample is composed of uniform core-shell nanoplates with 10-20 nm thickness, 80-100 nm landscape dimensions (aspect ratio ∼5) and 3-4 nm thickness of the surface shells. We used computational methods for the quantitative analysis of the core-shell particle structure and circularity shape descriptor for the quantitative shape analysis of the nanoparticles from TEM micrographs. The calculated results indicated that a percentage of the shell area in the nanoparticle area (share [%]) is significant. The determined values of circularity in the perpendicular and oblique perspective clearly show shape anisotropy of the nanoplates. The magnetic properties revealed the ferromagnetic-like properties at room temperature with high coercivity HC = 2340 Oe, pointing to the shape and surface effects. These results signify core-shell hematite nanoparticles' for practical applications in magnetic devices. The synthesized hematite plate-like nanoparticles exhibit low cytotoxicity levels on the human lung fibroblasts (MRC5) cell line demonstrating the safe use of these nanoparticles for biomedical applications.

CARBON-ENHANCED METAL-POOR STARS IN THE INNER AND OUTER HALO COMPONENTS OF THE MILKY WAY

International Nuclear Information System (INIS)

Carollo, Daniela; Norris, John E.; Freeman, Ken C.; Beers, Timothy C.; Lee, Young Sun; Kennedy, Catherine R.; Bovy, Jo; Sivarani, Thirupathi; Aoki, Wako

2012-01-01

Carbon-enhanced metal-poor (CEMP) stars in the halo components of the Milky Way are explored, based on accurate determinations of the carbon-to-iron ([C/Fe]) abundance ratios and kinematic quantities for over 30,000 calibration stars from the Sloan Digital Sky Survey. Using our present criterion that low-metallicity stars exhibiting [C/Fe] ratios ( c arbonicity ) in excess of [C/Fe] =+0.7 are considered CEMP stars, the global frequency of CEMP stars in the halo system for [Fe/H] 5 kpc, the CarDF exhibits a strong tail toward high values, up to [C/Fe] > +3.0. We also find a clear increase in the CEMP frequency with |Z|. For stars with –2.0 < [Fe/H] <–1.5, the frequency grows from 5% at |Z| ∼2 kpc to 10% at |Z| ∼10 kpc. For stars with [Fe/H] <–2.0, the frequency grows from 8% at |Z| ∼2 kpc to 25% at |Z| ∼10 kpc. For stars with –2.0 < [Fe/H] <–1.5, the mean carbonicity is ([C/Fe]) ∼+1.0 for 0 kpc < |Z| < 10 kpc, with little dependence on |Z|; for [Fe/H] <–2.0, ([C/Fe]) ∼+1.5, again roughly independent of |Z|. Based on a statistical separation of the halo components in velocity space, we find evidence for a significant contrast in the frequency of CEMP stars between the inner- and outer-halo components—the outer halo possesses roughly twice the fraction of CEMP stars as the inner halo. The carbonicity distribution also differs between the inner-halo and outer-halo components—the inner halo has a greater portion of stars with modest carbon enhancement ([C/Fe] ∼+0.5]); the outer halo has a greater portion of stars with large enhancements ([C/Fe] ∼+2.0), although considerable overlap still exists. We interpret these results as due to the possible presence of additional astrophysical sources of carbon production associated with outer-halo stars, beyond the asymptotic giant-branch source that may dominate for inner-halo stars, with implications for the progenitors of these populations.

Anticavitation and Differential Growth in Elastic Shells

KAUST Repository

Moulton, Derek E.; Goriely, Alain

2010-01-01

infinite growth or resorption is imposed at the inner surface of the shell. However, void collapse can occur in a limiting sense when radial and circumferential growth are properly balanced. Growth functions which diverge or vanish at a point arise

Geochemical gradients within modern and fossil shells of Concholepas concholepas from northern Chile: an insight into U-Th systematics and diagenetic/authigenic isotopic imprints in mollusk shells

Science.gov (United States)

Labonne, Maylis; Hillaire-Marcel, Claude

2000-05-01

Seriate geochemical measurements through shells of one modern, one Holocene, and two Sangamonian Concholepas concholepas, from marine terraces of Northern Chile, were performed to document diagenetic vs. authigenic geochemical signatures, and to better interpret U-series ages on such material. Subsamples were recovered by drilling from the outer calcitic layer to the inner aragonitic layer of each of the studied shells. Unfortunately, this sampling procedure induces artifacts, notably the convertion of up to ˜20% of calcite into aragonite, and of up to ˜6% of aragonite into calcite, as well as in the epimerization of a few percent of isoleucine into D-alloisoleucine/ L-isoleucine. Negligible sampling artifacts were noticed for stable isotope and total amino acid contents. Diagenetic effects on the geochemical properties of the shells are particularly pronounced in the inner aragonitic layer and more discrete in the outer calcitic layer. The time-dependent decay of the organic matrix of the shell is illustrated by a one order of magnitude lower total amino acid content in the Sangamonian specimens by comparison with the modern shell. Conversely, the Sangamonian shells U contents increase by a similar factor and 13C- 18O enrichments as high as 2 to 3‰ seem also to occur through the same time interval possibly due to partial replacement of aragonite by gypsum. The decay of the organic matrix of the aragonitic layer of the shell is thought to play a major role with respect to U-uptake processes and stable isotope shifts. Nevertheless, asymptotic 230Th-ages (˜100 ka) in the inner U-rich layers of the Sangamonian shells, and 234U/ 238U ratios compatible with a marine origin for U, suggest U-uptake within a short diagenetic interval, when marine waters were still bathing the embedding sediment. Thus, U-series ages on fossil mollusks from such a hyper-arid environment should not differ much from the age of the corresponding marine unit deposition. However, the

Core–shell Fe{sub 3}O{sub 4}–Au magnetic nanoparticles based nonenzymatic ultrasensitive electrochemiluminescence immunosensor using quantum dots functionalized graphene sheet as labels

Energy Technology Data Exchange (ETDEWEB)

Liu, Weiyan; Zhang, Yan [Key Laboratory of Chemical Sensing and Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022 (China); Ge, Shenguang [Shandong Provincial Key Laboratory of Preparation and Measurement of Building Materials, University of Jinan, Jinan 250022 (China); Song, Xianrang [Cancer Research Center, Shandong Tumor Hospital, Jinan 250012 (China); Huang, Jiadong [Key Laboratory of Chemical Sensing and Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022 (China); Yan, Mei, E-mail: chm_yanm@ujn.edu.cn [Key Laboratory of Chemical Sensing and Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022 (China); Yu, Jinghua [Key Laboratory of Chemical Sensing and Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022 (China)

2013-04-03

Graphical abstract: Core–shell Fe{sub 3}O{sub 4}–Au magnetic nanoparticles and P-GS@QDs were prepared to immobilize Ab{sub 1} and Ab{sub 2} respectively and combined to fabricate a novel sandwich-type ECL immunosensor for detecting CA125 at low concentration. Highlights: ► ECL immunosensor for CA125 based on a microfluidic strategy with a homemade ECL cell was proposed. ► Core–shell Fe{sub 3}O{sub 4}–Au magnetic nanoparticles were employed as the carriers of the primary antibodies. ► CdTe quantum dots functionalized graphene sheet were used for signal amplification. -- Abstract: In this paper, a novel, low-cost electrochemiluminescence (ECL) immunosensor using core–shell Fe{sub 3}O{sub 4}–Au magnetic nanoparticles (AuMNPs) as the carriers of the primary antibody of carbohydrate antigen 125 (CA125) was designed. Graphene sheet (GS) with property of good conductivity and large surface area was a captivating candidate to amplify ECL signal. We successively synthesized functionalized GS by loading large amounts of quantum dots (QDs) onto the poly (diallyldimethyl-ammonium chloride) (PDDA) coated graphene sheet (P-GS@QDs) via self-assembly electrostatic reactions, which were used to label secondary antibodies. The ECL immunosensors coupled with a microfluidic strategy exhibited a wide detection range (0.005–50 U mL{sup −1}) and a low detection limit (1.2 mU mL{sup −1}) with the help of an external magnetic field to gather immunosensors. The method was evaluated with clinical serum sample, receiving good correlation with results from commercially available analytical procedure.

Surface protection in bio-shields via a functional soft skin layer: Lessons from the turtle shell.

Science.gov (United States)

Shelef, Yaniv; Bar-On, Benny

2017-09-01

The turtle shell is a functional bio-shielding element, which has evolved naturally to provide protection against predator attacks that involve biting and clawing. The near-surface architecture of the turtle shell includes a soft bi-layer skin coating - rather than a hard exterior - which functions as a first line of defense against surface damage. This architecture represents a novel type of bio-shielding configuration, namely, an inverse structural-mechanical design, rather than the hard-coated bio-shielding elements identified so far. In the current study, we used experimentally based structural modeling and FE simulations to analyze the mechanical significance of this unconventional protection architecture in terms of resistance to surface damage upon extensive indentations. We found that the functional bi-layer skin of the turtle shell, which provides graded (soft-softer-hard) mechanical characteristics to the bio-shield exterior, serves as a bumper-buffer mechanism. This material-level adaptation protects the inner core from the highly localized indentation loads via stress delocalization and extensive near-surface plasticity. The newly revealed functional bi-layer coating architecture can potentially be adapted, using synthetic materials, to considerably enhance the surface load-bearing capabilities of various engineering configurations. Copyright © 2017 Elsevier Ltd. All rights reserved.

Resistance switching characteristics of core–shell γ-Fe{sub 2}O{sub 3}/Ni{sub 2}O{sub 3} nanoparticles in HfSiO matrix

Energy Technology Data Exchange (ETDEWEB)

Zhou, Guangdong [Guizhou Institute of Technology, Guiyang 550003 (China); Wu, Bo, E-mail: fqwubo@zync.edu.cn [Institute of Theoretical Physics, Zunyi Normal College, Zunyi 563002 (China); School of Marine Science and Technology, Northwestern Polytechnical University, Xian 710072 (China); Liu, Xiaoqin; Li, Zhiling; Zhang, Shuangju [Guizhou Institute of Technology, Guiyang 550003 (China); Zhou, Ankun [Kunming Institute of Botany, Chineses Academy Sciences, Kunming 650201 (China); Yang, Xiude [Institute of Theoretical Physics, Zunyi Normal College, Zunyi 563002 (China)

2016-09-05

Core–shell γ-Fe{sub 2}O{sub 3}/Ni{sub 2}O{sub 3} nanoparticles are synthesized by chemical co-precipitation method. Resistive switching memory behaviors, which have resistance ON/OFF ratio of ∼10{sup 2} and excellent retention property, are observed in the Au/HfSiO/γ-Fe{sub 2}O{sub 3}/Ni{sub 2}O{sub 3}/HfSiO/Pt structure. Space charge limited current (SCLC) mechanism, which is supported by the fitting current–voltage results, is employed to know the resistive switching memory effects. The transportation of Oxygen vacancy Vo{sup 2+}, oxygen ion O{sup 2−}, recombination of oxygen atom and drive of external electric field are responsible for the ON or OFF states observed in device. - Highlights: • Bipolar resistance switching effects are detected in core–shell of γ-Fe{sub 2}O{sub 3}@Ni{sub 2}O{sub 3}. • The Ohimc conduction and space-charge-limited current play an important role in Low/High field. • Rapture of filament assisted by Vo{sup 2+}, O{sup 2−} and O{sub 2} recombination is responsible for switching. • Resistance switching memory highlights excellent retention properties after stress 100 cycles.

Determination of K shell absorption jump factors and jump ratios of 3d transition metals by measuring K shell fluorescence parameters

International Nuclear Information System (INIS)

Kaçal, Mustafa Recep; Han, İbrahim; Akman, Ferdi

2015-01-01

Energy dispersive X-ray fluorescence technique (EDXRF) has been employed for measuring K-shell absorption jump factors and jump ratios for Ti, Cr, Fe, Co, Ni and Cu elements. The jump factors and jump ratios for these elements were determined by measuring K shell fluorescence parameters such as the Kα X-ray production cross-sections, K shell fluorescence yields, Kβ-to-Kα X-rays intensity ratios, total atomic absorption cross sections and mass attenuation coefficients. The measurements were performed using a Cd-109 radioactive point source and an Si(Li) detector in direct excitation and transmission experimental geometry. The measured values for jump factors and jump ratios were compared with theoretically calculated and the ones available in the literature. - Highlights: • This work regard the K shell absorption jump ratios and jump factors of Ti, Cr, Fe, Co, Ni and Cu. • This paper presents the first measurement of these parameters using the experimental K shell fluorescence parameters. • A good agreement was found between experimental and theoretical values. • The EDXRF technique was suitable, precise and reliable for the measurement of these atomic parameters

Rutas de circulación e intercambio de sal en la provincia de Tunja, segunda mitad del siglo XVI

Directory of Open Access Journals (Sweden)

Blanca Ofelia Acuña Rodriguez

2018-02-01

Full Text Available A través de este texto se pretende dar a conocer cómo las rutas de circulación de sal en la Provincia de Tunja contribuyeron a configurar un gran espacio económico, que integró a las provincias de Santa Fe, Pamplona y Tunja en el Nuevo Reino de Granada, durante el siglo XVI. Se partió de una reflexión historiográfica relacionada con la circulación y el comercio de la sal, los medios de transporte y las rutas usadas por los indígenas y los españoles; a partir de las cuales se consolidó un espacio económico mediado por la producción y distribución de la sal, que convirtió a la provincia de Tunja en un eje articulador de relaciones entre los sitios productores de sal en la provincia de Santa Fe y los consumidores de las provincias de Tunja y Pamplona. Esta articulación regional facilitó tanto la circulación de productos de distintos pisos térmicos, como la integración de un amplio territorio colonial. Esto debido a que la localización de Tunja como lugar de paso y conexión entre las Provincias de Santafé, Pamplona y los Llanos de San Juan, hizo de esta ciudad y sus términos un atractivo para el asentamiento hispano, a la vez que generó, durante la segunda mitad del siglo XVI, la posibilidad para que se organizaran en toda la Provincia de Tunja, sitios de aposento, venta y reventa de productos importados de España y productos de la tierra, para el sustento y abastecimiento de las necesidades básicas, y de esta forma sacar provecho de las producciones locales como la sal, el hayo, el algodón, las mantas y otros productos.

Efficient charge carriers induced by extra outer-shell electrons in iron-pnictides: a comparison between Ni- and Co-doped CaFeAsF

International Nuclear Information System (INIS)

Zhang Min; Yu Yi; Tan Shun; Zhang Yuheng; Zhang Changjin; Zhang Lei; Qu Zhe; Ling Langsheng; Xi, Chuanying

2010-01-01

A comprehensive study of the difference between CaFe 1-x Ni x AsF and CaFe 1-x Co x AsF systems has been carried out by measuring the efficient charge carrier concentration, the valence states and the superconducting phase diagram. It is found that at the same doping level, Ni doping introduces nearly twice the number of charge carriers as Co doping. However, x-ray absorption near-edge spectroscopy measurements reveal that the valence state of Fe in both systems is close to 2, indicating that there is no valence mismatch. We suggest that the charge carriers in CaFe 1-x M x AsF (M=transition metal elements) are not induced by valence mismatch but come from the difference in the number of outer-shell electrons. We also suggest that with Ni and Co doping, the systems change from a multi-band material in the underdoped regions to a single-band state in the overdoped regions.

Sub-10 nm Fe3O4@Cu2-xS core-shell nanoparticles for dual-modal imaging and photothermal therapy

KAUST Repository

Tian, Qiwei

2013-06-12

Photothermal nanomaterials have recently attracted significant research interest due to their potential applications in biological imaging and therapeutics. However, the development of small-sized photothermal nanomaterials with high thermal stability remains a formidable challenge. Here, we report the rational design and synthesis of ultrasmall (<10 nm) Fe3O 4@Cu2-xS core-shell nanoparticles, which offer both high photothermal stability and superparamagnetic properties. Specifically, these core-shell nanoparticles have proven effective as probes for T 2-weighted magnetic resonance imaging and infrared thermal imaging because of their strong absorption at the near-infrared region centered around 960 nm. Importantly, the photothermal effect of the nanoparticles can be precisely controlled by varying the Cu content in the core-shell structure. Furthermore, we demonstrate in vitro and in vivo photothermal ablation of cancer cells using these multifunctional nanoparticles. The results should provide improved understanding of synergistic effect resulting from the integration of magnetism with photothermal phenomenon, important for developing multimode nanoparticle probes for biomedical applications. © 2013 American Chemical Society.

Sub-10 nm Fe3O4@Cu2-xS core-shell nanoparticles for dual-modal imaging and photothermal therapy

KAUST Repository

Tian, Qiwei; Hu, Junqing; Zhu, Yihan; Zou, Rujia; Chen, Zhigang; Yang, Shiping; Li, Runwei; Su, Qianqian; Han, Yu; Liu, Xiaogang

2013-01-01

Photothermal nanomaterials have recently attracted significant research interest due to their potential applications in biological imaging and therapeutics. However, the development of small-sized photothermal nanomaterials with high thermal stability remains a formidable challenge. Here, we report the rational design and synthesis of ultrasmall (<10 nm) Fe3O 4@Cu2-xS core-shell nanoparticles, which offer both high photothermal stability and superparamagnetic properties. Specifically, these core-shell nanoparticles have proven effective as probes for T 2-weighted magnetic resonance imaging and infrared thermal imaging because of their strong absorption at the near-infrared region centered around 960 nm. Importantly, the photothermal effect of the nanoparticles can be precisely controlled by varying the Cu content in the core-shell structure. Furthermore, we demonstrate in vitro and in vivo photothermal ablation of cancer cells using these multifunctional nanoparticles. The results should provide improved understanding of synergistic effect resulting from the integration of magnetism with photothermal phenomenon, important for developing multimode nanoparticle probes for biomedical applications. © 2013 American Chemical Society.

Magnetization measurements and XMCD studies on ion irradiated iron oxide and core-shell iron/iron-oxide nanomaterials

Energy Technology Data Exchange (ETDEWEB)

Kaur, Maninder; Qiang, You; Jiang, Weilin; Pearce, Carolyn; McCloy, John S.

2014-12-02

Magnetite (Fe3O4) and core-shell iron/iron-oxide (Fe/Fe3O4) nanomaterials prepared by a cluster deposition system were irradiated with 5.5 MeV Si2+ ions and the structures determined by x-ray diffraction as consisting of 100% magnetite and 36/64 wt% Fe/FeO, respectively. However, x-ray magnetic circular dichroism (XMCD) indicates similar surfaces in the two samples, slightly oxidized and so having more Fe3+ than the expected magnetite structure, with XMCD intensity much lower for the irradiated core-shell samples indicating weaker magnetism. X-ray absorption spectroscopy (XAS) data lack the signature for FeO, but the irradiated core-shell system consists of Fe-cores with ~13 nm of separating oxide crystallite, so it is likely that FeO exists deeper than the probe depth of the XAS (~5 nm). Exchange bias (Hex) for both samples becomes increasingly negative as temperature is lowered, but the irradiated Fe3O4 sample shows greater sensitivity of cooling field on Hex. Loop asymmetries and Hex sensitivities of the irradiated Fe3O4 sample are due to interfaces and interactions between grains which were not present in samples before irradiation as well as surface oxidation. Asymmetries in the hysteresis curves of the irradiated core/shell sample are related to the reversal mechanism of the antiferromagnetic FeO and possibly some near surface oxidation.

Gypsum crystals in the inner shelf sediments off Maharashtra, India

Digital Repository Service at National Institute of Oceanography (India)

Hashimi, N.H.; Ambre, N.V.

Gypsum crystals have been found in the inner shelf silty clay/clayey silt off the Maharashtra Coast between Vengurla and Bombay. Generally these occur as euhedral single or twinned crystals of selenite. Very often shells are found embedded within...

Model uncertainties of local-thermodynamic-equilibrium K-shell spectroscopy

Science.gov (United States)

Nagayama, T.; Bailey, J. E.; Mancini, R. C.; Iglesias, C. A.; Hansen, S. B.; Blancard, C.; Chung, H. K.; Colgan, J.; Cosse, Ph.; Faussurier, G.; Florido, R.; Fontes, C. J.; Gilleron, F.; Golovkin, I. E.; Kilcrease, D. P.; Loisel, G.; MacFarlane, J. J.; Pain, J.-C.; Rochau, G. A.; Sherrill, M. E.; Lee, R. W.

2016-09-01

Local-thermodynamic-equilibrium (LTE) K-shell spectroscopy is a common tool to diagnose electron density, ne, and electron temperature, Te, of high-energy-density (HED) plasmas. Knowing the accuracy of such diagnostics is important to provide quantitative conclusions of many HED-plasma research efforts. For example, Fe opacities were recently measured at multiple conditions at the Sandia National Laboratories Z machine (Bailey et al., 2015), showing significant disagreement with modeled opacities. Since the plasma conditions were measured using K-shell spectroscopy of tracer Mg (Nagayama et al., 2014), one concern is the accuracy of the inferred Fe conditions. In this article, we investigate the K-shell spectroscopy model uncertainties by analyzing the Mg spectra computed with 11 different models at the same conditions. We find that the inferred conditions differ by ±20-30% in ne and ±2-4% in Te depending on the choice of spectral model. Also, we find that half of the Te uncertainty comes from ne uncertainty. To refine the accuracy of the K-shell spectroscopy, it is important to scrutinize and experimentally validate line-shape theory. We investigate the impact of the inferred ne and Te model uncertainty on the Fe opacity measurements. Its impact is small and does not explain the reported discrepancies.

Nanospherical inorganic α-Fe core-organic shell necklaces for the removal of arsenic(V) and chromium(VI) from aqueous solution

Science.gov (United States)

Azzam, Ahmed M.; Shenashen, Mohamed A.; Selim, Mahmoud M.; Yamaguchi, Hitoshi; El-Sewify, Islam M.; Kawada, Satoshi; Alhamid, Abdulaziz A.; El-Safty, Sherif A.

2017-10-01

Mesoporous nanospherical necklaces (NSN) of inorganic α-Fe core-organic shell and ethylenediaminetetraacetic acid (EDTA) were fabricated. The necklaces were 1 μm in length and 50 nm in thickness, with massive nanospherical particles connecting and overlapping in a neat micro-/nano-necklace archery cage for capturing/trapping of As(V) and Cr(VI) species from water sources. The α-Fe core and the dressing shell of EDTA provided numerous active sites for adsorption, which led to 100% adsorption uptake of these toxic ions. The adsorption isotherms revealed that NSN adsorbent with mesoporous caves and organic-decorated surfaces was promising and effective for the spontaneous and endothermic removal of both ions from contaminated water. The NSN structure exhibited long-term stability. The adsorption efficiency and uptake of the deleterious arsenic and chromium species were achieved after multi-particulate processing of reuse cycles. The pH-dependent removal of As(V) and Cr(VI) species is an emerging topic in selective adsorption assays among competitive ions. Furthermore, the ion-selective conditions at pH 5 for As(V) and pH 7 for Cr(VI) significantly affected the adsorption capacity and affinity of 306.7 and 406.5 mg g-1 into NSN cages, respectively. The obtained results could be used as a basis to provide effective and low-cost products for the purification of wastewater resources from toxic metals.

Thermodynamical properties of 56Fe

International Nuclear Information System (INIS)

Tavukcu, E.; Becker, J. A.; Bernstein, L. A.; Garrett, P. E.; Younes, W.; Guttormsen, M.; Rekstad, J.; Siem, S.; Mitchell, G. E.; Schiller, A.; Voinov, A.

2003-01-01

Average nuclear level densities close to the nuclear binding energy in 56Fe and 57Fe are extracted from primary γ-ray spectra. A step structure is observed in the level density for both isotopes, and is interpreted as breaking of Cooper pairs. Thermal properties of 56Fe are studied within the statistical canonical ensemble. The experimental heat capacity in 56Fe is compared with the theoretical heat capacity calculated within the shell model Monte Carlo approach

Mango core inner shell membrane template-directed synthesis of porous ZnO films and their application for enzymatic glucose biosensor

Science.gov (United States)

Zhou, Yu; Wang, Lei; Ye, Zhizhen; Zhao, Minggang; Cai, Hui; Huang, Jingyun

2013-11-01

Micro/nano-porous ZnO films were synthesized through a simple biotemplate-directed method using mango core inner shell membranes as templates. The achieved ZnO films with wrinkles on the surface are combined of large holes and small pores in the bulk. High specific surface area, numerous microspaces, and small channels for fluid circulation provided by this unique structure along with the good biocompatibility and electron communication features of ZnO material make the product an ideal platform for the immobilization of enzymes The fabricated glucose biosensor based on the porous ZnO films exhibits good selective detection ability of analyte with good stability, high sensitivity of 50.58 μA cm-2 mM-1 and a wide linear range of 0.2-5.6 mM along with a low detection limit of 10 μM.

Statistical modeling of the reactions Fe(+) + N2O → FeO(+) + N2 and FeO(+) + CO → Fe(+) + CO2.

Science.gov (United States)

Ushakov, Vladimir G; Troe, Jürgen; Johnson, Ryan S; Guo, Hua; Ard, Shaun G; Melko, Joshua J; Shuman, Nicholas S; Viggiano, Albert A

2015-08-14

The rates of the reactions Fe(+) + N2O → FeO(+) + N2 and FeO(+) + CO → Fe(+) + CO2 are modeled by statistical rate theory accounting for energy- and angular momentum-specific rate constants for formation of the primary and secondary cationic adducts and their backward and forward reactions. The reactions are both suggested to proceed on sextet and quartet potential energy surfaces with efficient, but probably not complete, equilibration by spin-inversion of the populations of the sextet and quartet adducts. The influence of spin-inversion on the overall reaction rate is investigated. The differences of the two reaction rates mostly are due to different numbers of entrance states (atom + linear rotor or linear rotor + linear rotor, respectively). The reaction Fe(+) + N2O was studied either with (6)Fe(+) or with (4)Fe(+) reactants. Differences in the rate constants of (6)Fe(+) and (4)Fe(+) reacting with N2O are attributed to different contributions from electronically excited potential energy surfaces, such as they originate from the open-electronic shell reactants.

Inverse estimation of heat flux and temperature on nozzle throat-insert inner contour

Energy Technology Data Exchange (ETDEWEB)

Chen, Tsung-Chien [Department of Power Vehicle and Systems Engineering, Chung Cheng Institute of Technology, National Defense University, Ta-Hsi, Tao-Yuan 33509 (China); Liu, Chiun-Chien [Chung Shan Institute of Science and Technology, Lung-Tan, Tao-Yuan 32526 (China)

2008-07-01

During the missile flight, the jet flow with high temperature comes from the heat flux of propellant burning. An enormous heat flux from the nozzle throat-insert inner contour conducted into the nozzle shell will degrade the material strength of nozzle shell and reduce the nozzle thrust efficiency. In this paper, an on-line inverse method based on the input estimation method combined with the finite-element scheme is proposed to inversely estimate the unknown heat flux on the nozzle throat-insert inner contour and the inner wall temperature by applying the temperature measurements of the nozzle throat-insert. The finite-element scheme can easily define the irregularly shaped boundary. The superior capability of the proposed method is demonstrated in two major time-varying estimation cases. The computational results show that the proposed method has good estimation performance and highly facilitates the practical implementation. An effective analytical method can be offered to increase the operation reliability and thermal-resistance layer design in the solid rocket motor. (author)

Sound transmission through double cylindrical shells lined with porous material under turbulent boundary layer excitation

Science.gov (United States)

Zhou, Jie; Bhaskar, Atul; Zhang, Xin

2015-11-01

This paper investigates sound transmission through double-walled cylindrical shell lined with poroelastic material in the core, excited by pressure fluctuations due to the exterior turbulent boundary layer (TBL). Biot's model is used to describe the sound wave propagating in the porous material. Three types of constructions, bonded-bonded, bonded-unbonded and unbonded-unbonded, are considered in this study. The power spectral density (PSD) of the inner shell kinetic energy is predicted for two turbulent boundary layer models, different air gap depths and three types of polyimide foams, respectively. The peaks of the inner shell kinetic energy due to shell resonance, hydrodynamic coincidence and acoustic coincidence are discussed. The results show that if the frequency band over the ring frequency is of interest, an air gap, even if very thin, should exist between the two elastic shells for better sound insulation. And if small density foam has a high flow resistance, a superior sound insulation can still be maintained.

Autoradiographic study on the distribution of 241Am in the shell of the freshwater zebra mussel Dreissena polymorpha

International Nuclear Information System (INIS)

Zuykov, M.; Pelletier, E.; Rouleau, C.; Popov, L.; Fowler, S.W.; Orlova, M.

2009-01-01

Autoradiography was used to identify α-track distributions in a series of shell sections from live mussels Dreissena polymorpha Pallas and dissected shells of dead mussels obtained from laboratory experiments using relatively high concentrations of 241 Am in the exposure media, a required condition for successful use of this autoradiographic technique. A comparable distribution of α-tracks was recorded on autoradiographs from both live and dead shells suggesting that metabolism does not lead to any sizable changes in the process of 241 Am adsorption (present in the extrapallial fluid) onto the inner surface of shell. Autoradiographs showed a preferential accumulation of 241 Am in the organic periostracum, whereas the outer and inner shell layers were characterized by a relatively low α-tracks density. No α-tracks were observed in the central part of the shell in any of the samples. These observations will be useful for the development of a general model to explain bioaccumulation and biosorption processes of radionuclides into mollusk shells. (author)

Double shell planar experiments on OMEGA

Science.gov (United States)

Dodd, E. S.; Merritt, E. C.; Palaniyappan, S.; Montgomery, D. S.; Daughton, W. S.; Schmidt, D. W.; Cardenas, T.; Wilson, D. C.; Loomis, E. N.; Batha, S. H.; Ping, Y.; Smalyuk, V. A.; Amendt, P. A.

2017-10-01

The double shell project is aimed at fielding neutron-producing capsules at the National Ignition Facility (NIF), in which an outer low-Z ablator collides with an inner high-Z shell to compress the fuel. However, understanding these targets experimentally can be challenging when compared with conventional single shell targets. Halfraum-driven planar targets at OMEGA are being used to study physics issues important to double shell implosions outside of a convergent geometry. Both VISAR and radiography through a tube have advantages over imaging through the hohlraum and double-shell capsule at NIF. A number physics issues are being studied with this platform that include 1-d and higher dimensional effects such as defect-driven hydrodynamic instabilities from engineering features. Additionally, the use of novel materials with controlled density gradients require study in easily diagnosed 1-d systems. This work ultimately feeds back into the NIF capsule platform through manufacturing tolerances set using data from OMEGA. Supported under the US DOE by the LANS, LLC under contract DE-AC52-06NA25396. LA-UR-17-25386.

Study of characterization of trace elements in marine shells of Sambaqui: correlation between recent and old shells

International Nuclear Information System (INIS)

Gomez, Mauro Roger Batista Pousada; Rocha, Flavio Roberto; Silva, Paulo Sergio Cardoso da

2013-01-01

Calcium carbonate of recent and ancient C. rhizophorae oyster shells was analyzed for the determination of trace elements by instrumental neutron activation analysis. The ancient shells belong to a Sambaqui located in Cananeia region, South of Sao Paulo state and the recent ones are from an oyster production farm in the same region Studies related to the element concentrations in molluscs shell has been done as a tentative of establishing the element concentrations with palio-environmental factor. In this study it was aimed to verify differences in the elemental constitution of recent and ancient oyster shells that present potential for being used as indicator of marine changes. Results indicated that the elements Br, Ce, La, Na, Sm and An are higher in recent shells and the elements Cr, Fe Sc and Th are higher in ancient shells. Statistical analyses performed indicated that the enrichment of the light rare earth elements related to Ca are possibly good candidates for these palio-environmental studies. (author)

Experimental evaluation of inner-vacancy level energies for comparison with theory

International Nuclear Information System (INIS)

Deslattes, R.D.; Kessler, E.G.

1985-01-01

This chapter deals with progress on the theoretical side in calculations of atomic inner-shell energy levels. In reaching what the authors consider to be the best available body of experimental data about inner-shell energy-level differences, three types of input are used: those lines which have been directly measured with high-resolution double-diffraction instruments; those obtained with high-resolution curved-crystal optics relative to gamma-ray standards, and those (low-energy) lines whose wavelength ratios with respect to directly measured X-ray lines have been taken from a very restricted set of earlier measurements. Application of X-ray absorption spectroscopy (XAS), X-ray photoelectron spectroscopy (XPS), Auger electron spectroscopy (AES), appearance-potential spectroscopy (APS), and X-ray emission spectroscopy (XES) to the problem of energy-level difference determination and single-vacancy energy level determination are described

Core-shell magnetic nanoparticles for on-chip RF inductors

KAUST Repository

Koh, Kisik

2013-01-01

FeNi3 based core-shell magnetic nanoparticles are demonstrated as the magnetic core material for on-chip, radio frequency (RF) inductors. FeNi3 nanoparticles with 50-150 nm in diameter with 15-20 nm-thick SiO2 coating are chemically synthesized and deposited on a planar inductor as the magnetic core to enhance both inductance (L) and quality factor (Q) of the inductor. Experimentally, the ferromagnetic resonant frequency of the on-chip inductors based on FeNi3 core-shell nanoparticles has been shown to be over several GHz. A post-CMOS process has been developed to integrate the magnetic nanoparticles to a planar inductor and inductance enhancements up to 50% of the original magnitude with slightly enhanced Q-factor up to 1 GHz have been achieved. © 2013 IEEE.

One-pot synthesis and characterization of rhodamine derivative-loaded magnetic core-shell nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Zhang Jin, E-mail: jzhang@eng.uwo.ca; Li Jiaxin [University of Western Ontario, Department of Chemical and Biochemical Engineering (Canada); Razavi, Fereidoon S. [Brock University, Department of Physics (Canada); Mumin, Abdul Md. [University of Western Ontario, Department of Chemical and Biochemical Engineering (Canada)

2011-05-15

A new method to produce elaborate nanostructure with magnetic and fluorescent properties in one entity is reported in this article. Magnetite (Fe{sub 3}O{sub 4}) coated with fluorescent silica (SiO{sub 2}) shell was produced through the one-pot reaction, in which one reactor was utilized to realize the synthesis of superparamagnetic core of Fe{sub 3}O{sub 4}, the formation of SiO{sub 2} coating through the condensation and polymerization of tetraethylorthosilicate (TEOS), and the encapsulation of tetramethyl rhodamine isothiocyanate-dextran (TRITC-dextran) within silica shell. Transmission electron microscopy (TEM), energy dispersive X-ray (EDX) analysis, and X-ray diffraction (XRD) were carried out to investigate the core-shell structure. The magnetic core of the core-shell nanoparticles is 60 {+-} 10 nm in diameter. The thickness of the fluorescent SiO{sub 2} shell is estimated at 15 {+-} 5 nm. In addition, the fluorescent signal of the SiO{sub 2} shell has been detected by the laser confocal scanning microscopy (LCSM) with emission wavelength ({lambda}{sub em}) at 566 nm. In addition, the magnetic properties of TRITC-dextran loaded silica-coating iron oxide nanoparticles (Fe{sub 3}O{sub 4}-SiO{sub 2} NPs) were studied. The hysteresis loop of the core-shell NPs measured at room temperature shows that the saturation magnetization (M{sub s}) is not reached even at the field of 70 kOe (7T). Meanwhile, the very low coercivity (H{sub c}) and remanent magnetization (M{sub r}) are 0.375 kOe and 6.6 emu/g, respectively, at room temperature. It indicates that the core-shell particles have the superparamagnetic properties. The measured blocking temperature (T{sub B}) of the TRITC-dextran loaded Fe{sub 3}O{sub 4}-SiO{sub 2} NPs is about 122.5 K. It is expected that the multifunctional core-shell nanoparticles can be used in bio-imaging.

Gas phase synthesis of core-shell Fe@FeO{sub x} magnetic nanoparticles into fluids

Energy Technology Data Exchange (ETDEWEB)

Aktas, Sitki, E-mail: aksitki61@gmail.com; Thornton, Stuart C.; Binns, Chris [University of Leicester, Department of Physics and Astronomy (United Kingdom); Denby, Phil [Ensol As, Nesttun (Norway)

2016-12-15

Sorbitol, short chain molecules, have been used to stabilise of Fe@FeO{sub x} nanoparticles produced in the gas phase under the ultra-high vacuum (UHV) conditions. The sorbitol coated Fe@FeO{sub x} nanoparticles produced by our method have a narrow size distribution with a hydrodynamic diameter of 35 nm after NaOH is added to the solution. Magnetisation measurement shows that the magnetic nanoparticles are superparamagnetic at 100 K and demonstrate hysteresis at 5 K with an anisotropy constant of 5.31 × 10{sup 4} J/m{sup 3} (similar to bulk iron). Also, it is shown that sorbitol is only suitable for stabilising the Fe@FeO{sub x} suspensions, and it does not prevent further oxidation of the metallic Fe core. According to MRI measurement, the nanoparticles have a high transverse relaxation rate of 425 mM{sup −1} s{sup −1}.

Average L-shell fluorescence, Auger, and electron yields

International Nuclear Information System (INIS)

Krause, M.O.

1980-01-01

The dependence of the average L-shell fluorescence and Auger yields on the initial vacancy distribution is shown to be small. By contrast, the average electron yield pertaining to both Auger and Coster-Kronig transitions is shown to display a strong dependence. Numerical examples are given on the basis of Krause's evaluation of subshell radiative and radiationless yields. Average yields are calculated for widely differing vacancy distributions and are intercompared graphically for 40 3 subshell yields in most cases of inner-shell ionization

Shell Inspection History and Current CMM Inspection Efforts

Energy Technology Data Exchange (ETDEWEB)

Montano, Joshua Daniel [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

2017-01-26

The following report provides a review of past and current CMM Shell Inspection efforts. Calibration of the Sheffield rotary contour gauge has expired and the primary inspector, Matthew Naranjo, has retired. Efforts within the Inspection team are transitioning from maintaining and training new inspectors on Sheffield to off-the-shelf CMM technology. Although inspection of a shell has many requirements, the scope of the data presented in this report focuses on the inner contour, outer contour, radial wall thickness and mass comparisons.

Moscow Autocracy of XVI - XVII Centuries: Eastern ‘’Despotism’’ or an Early Modern European Monarchy?

Directory of Open Access Journals (Sweden)

Vasilij A. Zajcev

2017-06-01

Full Text Available The article considers the problems related to the peculiarities of the Russian state political and legal development during the early New Time (XVI-XVII centuries in a comparative-historical aspect against the background of similar processes taking place in neighboring European states. The authors come to the conclusion that, despite certain, dictated by objective reasons (first of all, the conditions for the emergence and subsequent development, there are more common features than the differences between the processes of the political and legal sphere development in Russia and Western Europe. The fact that this community escaped from the view of researchers is related, in the authors' opinion, to the fact that foreign observers, describing the political system of an early Russian state, dealt only with an outer shell, while its internal contents remained if not a secret, then, in any case, a mystery for them. They were not admitted to the Russian political cuisine, and therefore the details of Russian political and legal institution functioning remained unavailable to them.

Mango core inner shell membrane template-directed synthesis of porous ZnO films and their application for enzymatic glucose biosensor

Energy Technology Data Exchange (ETDEWEB)

Zhou, Yu; Wang, Lei [Department of Materials Science and Engineering, State Key Laboratory of Silicon Materials, Zhejiang University, Hangzhou, 310027 (China); Ye, Zhizhen [Department of Materials Science and Engineering, State Key Laboratory of Silicon Materials, Zhejiang University, Hangzhou, 310027 (China); Cyrus Tang Center for Sensor Materials and Applications, Zhejiang University (China); Zhao, Minggang; Cai, Hui [Department of Materials Science and Engineering, State Key Laboratory of Silicon Materials, Zhejiang University, Hangzhou, 310027 (China); Huang, Jingyun, E-mail: huangjy@zju.edu.cn [Department of Materials Science and Engineering, State Key Laboratory of Silicon Materials, Zhejiang University, Hangzhou, 310027 (China); Cyrus Tang Center for Sensor Materials and Applications, Zhejiang University (China)

2013-11-15

Micro/nano-porous ZnO films were synthesized through a simple biotemplate-directed method using mango core inner shell membranes as templates. The achieved ZnO films with wrinkles on the surface are combined of large holes and small pores in the bulk. High specific surface area, numerous microspaces, and small channels for fluid circulation provided by this unique structure along with the good biocompatibility and electron communication features of ZnO material make the product an ideal platform for the immobilization of enzymes The fabricated glucose biosensor based on the porous ZnO films exhibits good selective detection ability of analyte with good stability, high sensitivity of 50.58 μA cm{sup −2} mM{sup −1} and a wide linear range of 0.2–5.6 mM along with a low detection limit of 10 μM.

Synthesis and electrochemical properties of Fe3O4@MOF core-shell microspheres as an anode for lithium ion battery application

Science.gov (United States)

Sun, Xuemin; Gao, Ge; Yan, Dongwei; Feng, Chuanqi

2017-05-01

The Fe3O4@MOF composite with a microspheric core and a porous metal-organic framework (MOF HKUST-1) shell has been successfully synthesized utilizing a versatile Layer-by-Layer (LBL) assembly method. The structure was identified by X-ray diffraction (XRD), and the morphology was investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques. The Fe3O4@MOF composite exhibited outstanding electrochemical properties when it was used as an anode material for lithium ion batteries (LIBs). After 100 discharge-charge cycles at a current density of 100 mA g-1, the reversible capacity of Fe3O4@MOF could maintain ∼1002 mAh g-1, which was much higher than that of the bare Fe3O4 counterpart (696 mAh g-1). Moreover, load the current density as high as 2 A g-1 (after 70 cycles at the current density step increased from 0.1 to 2 A g-1), it still delivered a reversible capacity of ∼429 mAh g-1. The results demonstrate that the cycling stability of Fe3O4 as an anode could be significantly improved by coating Cu3(1,3,5-benzenetricarboxylate)2 (HKUST-1). This strategy may offer new route to prepare other composite materials using different particles and suitable Metal-organic frameworks (MOFs) for LIBs application.

Geochemical Constraints on Core-Mantle Interaction from Fe/Mn Ratios

Science.gov (United States)

Humayun, M.; Qin, L.

2003-12-01

The greater density of liquid iron alloy, and its immiscibility with silicate, maintains the physical separation of the core from the mantle. There are no a priori reasons, however, why the Earth's mantle should be chemically isolated from the core. Osmium isotopic variations in mantle plumes have been interpreted in terms of interaction between outer core and the source regions of deep mantle plumes. If chemical transport occurs across the core-mantle boundary its mechanism remains to be established. The Os isotope evidence has also been interpreted as the signatures of subducted Mn-sediments, which are known to have relatively high Pt/Os. In the mantle, Fe occurs mainly as the divalent ferrous ion, and Mn occurs solely as a divalent ion, and both behave in a geochemically coherent manner because of similarity in ionic charge and radius. Thus, the Fe/Mn ratio is a planetary constant insensitive to processes of mantle differentiation by partial melting. Two processes may perturb the ambient mantle Fe/Mn of 60: a) the subduction of Mn-sediments should decrease the Fe/Mn ratio in plume sources, while b) chemical transport from the outer core may increase the Fe/Mn ratio. The differentiation of the liquid outer core to form the solid inner core may increase abundances of the light element constituents (FeS, FeO, etc.) to the point of exsolution from the core at the CMB. The exact rate of this process is determined by the rate of inner core growth. Two end-member models include 1) inner core formation mainly prior to 3.5 Ga with heat release dominated by radioactive sources, or 2) inner core formation occurring mainly in the last 1.5 Ga with heat release dominated by latent heat. This latter model would imply large fluxes of Fe into the sources of modern mantle plumes. Existing Fe/Mn data for Gorgona and Hawaiian samples place limits on both these processes. We describe a new procedure for the precise determination of the Fe/Mn ratio in magmatic rocks by ICP-MS. This

Synthesis of Magnetic Rattle-Type Silica with Controllable Magnetite and Tunable Size by Pre-Shell-Post-Core Method.

Science.gov (United States)

Chen, Xue; Tan, Longfei; Meng, Xianwei

2016-03-01

In this study, we have developed the pre-shell-post-core route to synthesize the magnetic rattle-type silica. This method has not only simplified the precursor's process and reduced the reacting time, but also ameliorated the loss of magnetite and made the magnetite content and the inner core size controllable and tunable. The magnetite contents and inner core size can be easily controlled by changing the type and concentration of alkali, reaction system and addition of water. The results show that alkali aqueous solution promotes the escape of the precursor iron ions from the inner space of rattle-type silica and results in the loss of magnetite. In this case, NaOH ethanol solution is better for the formation of magnetite than ammonia because it not only offers an appropriate alkalinity to facilitate the synthesis of. magnetic particles, but also avoids the escape of the iron ions from the mesopores of rattle-type silica. The synthesis process is very simple and efficient, and it takes no more than 2 hours to complete the total preparation and handling of the magnetic rattle-type silica. The end-product Fe3O4@SiO2 nanocomposites also have good magnetic properties which will perform potential application in biomedical science.

Sonochemical synthesis of magnetic core-shell Fe{sub 3}O{sub 4}-ZrO{sub 2} nanoparticles and their application to the highly effective immobilization of myoglobin for direct electrochemistry

Energy Technology Data Exchange (ETDEWEB)

Peng Huaping; Liang Ruping; Zhang Li [Department of Chemistry, Nanchang University, Nanchang 330031 (China); Qiu Jianding, E-mail: jdqiu@ncu.edu.c [Department of Chemistry, Nanchang University, Nanchang 330031 (China)

2011-04-15

Graphical abstract: Display Omitted Highlights: Magnetic core-shell Fe{sub 3}O{sub 4}-ZrO{sub 2} nanoparticle was synthesized by sonochemical approach. Fe{sub 3}O{sub 4}-ZrO{sub 2} NPs provided high capacity for trapping Mb on magnetic glassy carbon electrode surface. The constructed Mb/Fe{sub 3}O{sub 4}-ZrO{sub 2} film exhibited excellent electrocatalytic ability for the reduction of H{sub 2}O{sub 2}. The proposed method simplifies the immobilization methodology of proteins. - Abstract: In this study, bifunctional Fe{sub 3}O{sub 4}-ZrO{sub 2} magnetic core-shell nanoparticles (NPs), synthesized by a simple and effective sonochemical approach, were attached to the surface of a magnetic glassy carbon electrode (MGCE) and successfully applied to the immobilization/adsorption of myoglobin (Mb) for constructing a novel biosensor platform. With the advantages of the magnetism and the excellent biocompatibility of the Fe{sub 3}O{sub 4}-ZrO{sub 2} NPs, Mb could be easily immobilized on the surface of the electrode in the present of external magnetic field and well retained its bioactivity, hence dramatically facilitated direct electron transfer of Mb was demonstrated. The proposed Mb/Fe{sub 3}O{sub 4}-ZrO{sub 2} biofilm electrode exhibited excellent electrocatalytic behaviors towards the reduction of H{sub 2}O{sub 2} with a linear range from 0.64 {mu}M to 148 {mu}M. This presented system avoids the complex synthesis for protecting Fe{sub 3}O{sub 4} NPs, supplies a simple, effective and inexpensive way to immobilize protein, and is promising for construction of third-generation biosensors and other bio-magnetic induction devices.

Transient response of rotating laminated functionally graded cylindrical shells in thermal environment

International Nuclear Information System (INIS)

Malekzadeh, P.; Heydarpour, Y.; Haghighi, M.R. Golbahar; Vaghefi, M.

2012-01-01

Based on the elasticity theory, the transient analysis of dynamically pressurized rotating multi-layered functionally graded (FG) cylindrical shells in thermal environment is presented. The variations of the field variables across the shell thickness are accurately modeled by dividing the shell into a set of co-axial mathematical layers in the radial direction. The initial thermo-mechanical stresses are obtained by solving the thermoelastic equilibrium equations. The differential quadrature method and Newmark's time integration scheme are employed to discretize the obtained governing equations of each mathematical layer. After performing the convergence and comparison studies, parametric studies for two common types of FG sandwich shells, namely, the shell with homogeneous inner/outer layers and FG core and the shell with FG inner/outer layers and homogeneous core are carried out. The influences of the temperature dependence of material properties, material graded index, the convective heat transfer coefficient, the angular velocity, the boundary condition and the geometrical parameters (length and thickness to outer radius ratios) on the dynamic response of the FG shells are investigated. Highlights: ► As a first endeavor, transient analysis of rotating laminated functionally graded cylinders. ► Employing an elasticity based discrete layer-differential quadrature method. ► Evaluating and including the initial thermo-mechanical stresses accurately. ► Considering the temperature-dependence of the material properties. ► Presenting some new results, which can be used as benchmark solution for future works.

Structural shell analysis understanding and application

CERN Document Server

Blaauwendraad, Johan

2014-01-01

The mathematical description of the properties of a shell is much more elaborate than those of beam and plate structures. Therefore many engineers and architects are unacquainted with aspects of shell behaviour and design, and are not familiar with sufficiently reliable shell theories for the different shell types as derived in the middle of the 20th century. Rather than contributing to theory development, this university textbook focuses on architectural and civil engineering schools. Of course, practising professionals will profit from it as well. The book deals with thin elastic shells, in particular with cylindrical, conical and spherical types, and with elliptic and hyperbolic paraboloids. The focus is on roofs, chimneys, pressure vessels and storage tanks. Special attention is paid to edge bending disturbance zones, which is indispensable knowledge in FE meshing. A substantial part of the book results from research efforts in the mid 20th century at Delft University of Technology. As such, it is a valua...

Synthesis and controllable oxidation of monodisperse cobalt-doped wüstite nanoparticles and their core-shell stability and exchange-bias stabilization.

Science.gov (United States)

Chen, Chih-Jung; Chiang, Ray-Kuang; Kamali, Saeed; Wang, Sue-Lein

2015-09-14

Cobalt-doped wüstite (CWT), Co0.33Fe0.67O, nanoparticles were prepared via the thermal decomposition of CoFe2-oleate complexes in organic solvents. A controllable oxidation process was then performed to obtain Co0.33Fe0.67O/CoFe2O4 core-shell structures with different core-to-shell volume ratios and exchange bias properties. The oxidized core-shell samples with a ∼4 nm CoFe2O4 shell showed good resistance to oxygen transmission. Thus, it is inferred that the cobalt ferrite shell provides a better oxidation barrier performance than magnetite in the un-doped case. The hysteresis loops of the oxidized 19 nm samples exhibited a high exchange bias field (H(E)), an enhanced coercivity field (H(C)), and a pronounced vertical shift, thus indicating the presence of a strong exchange bias coupling effect. More importantly, the onset temperature of H(E) was found to be higher than 200 K, which suggests that cobalt doping increases the Néel temperature (T(N)) of the CWT core. In general, the results show that the homogeneous dispersion of Co in iron precursors improves the stability of the final CWT nanoparticles. Moreover, the CoFe2O4 shells formed following oxidation increase the oxidation resistance of the CWT cores and enhance their anisotropy energy.

Reversible patterning of spherical shells through constrained buckling

Science.gov (United States)

Marthelot, J.; Brun, P.-T.; Jiménez, F. López; Reis, P. M.

2017-07-01

Recent advances in active soft structures envision the large deformations resulting from mechanical instabilities as routes for functional shape morphing. Numerous such examples exist for filamentary and plate systems. However, examples with double-curved shells are rarer, with progress hampered by challenges in fabrication and the complexities involved in analyzing their underlying geometrical nonlinearities. We show that on-demand patterning of hemispherical shells can be achieved through constrained buckling. Their postbuckling response is stabilized by an inner rigid mandrel. Through a combination of experiments, simulations, and scaling analyses, our investigation focuses on the nucleation and evolution of the buckling patterns into a reticulated network of sharp ridges. The geometry of the system, namely, the shell radius and the gap between the shell and the mandrel, is found to be the primary ingredient to set the surface morphology. This prominence of geometry suggests a robust, scalable, and tunable mechanism for reversible shape morphing of elastic shells.

Investigation of the accuracy of MV radiation isocentre calculations in the Elekta cone-beam CT software XVI

DEFF Research Database (Denmark)

Zimmermann, S. J.; Rowshanfarzad, P.; Ebert, M. A.

2015-01-01

) and the radiation field centre (RFC) is calculated. A software package was developed for accurate calculation of the linac isocentre position. This requires precise determination of the position of the ball bearing and the RFC. Results: Data were acquired for 6 MV, 18 MV and flattening filter free (FFF) 6 MV FFF...... radiation isocentre prior to routine use of the cone-beam CT system. The isocentre determination method used in the XVI software is not available to users. The aim of this work is to perform an independent evaluation of the Elekta XVI 4.5 software for isocentre verification with focus on the robustness...... iView GT software. Two images were acquired at each cardinal gantry angle (-180o, -90o , 0o, 90o) at two opposing collimator angles. The images were exported to the conebeam CT software XVI 4.5 where the difference between the ball bearing position in the XYZ-room coordinates (IEC61217...

Core-shell LiFePO4 /carbon-coated reduced graphene oxide hybrids for high-power lithium-ion battery cathodes.

Science.gov (United States)

Ha, Sung Hoon; Lee, Yun Jung

2015-01-26

Core-shell carbon-coated LiFePO4 nanoparticles were hybridized with reduced graphene (rGO) for high-power lithium-ion battery cathodes. Spontaneous aggregation of hydrophobic graphene in aqueous solutions during the formation of composite materials was precluded by employing hydrophilic graphene oxide (GO) as starting templates. The fabrication of true nanoscale carbon-coated LiFePO4 -rGO (LFP/C-rGO) hybrids were ascribed to three factors: 1) In-situ polymerization of polypyrrole for constrained nanoparticle synthesis of LiFePO4 , 2) enhanced dispersion of conducting 2D networks endowed by colloidal stability of GO, and 3) intimate contact between active materials and rGO. The importance of conducting template dispersion was demonstrated by contrasting LFP/C-rGO hybrids with LFP/C-rGO composites in which agglomerated rGO solution was used as the starting templates. The fabricated hybrid cathodes showed superior rate capability and cyclability with rates from 0.1 to 60 C. This study demonstrated the synergistic combination of nanosizing with efficient conducting templates to afford facile Li(+) ion and electron transport for high power applications. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Morphology and oxide shell structure of iron nanoparticles grown by sputter-gas-aggregation

International Nuclear Information System (INIS)

Wang, C M; Baer, D R; Amonette, J E; Engelhard, M H; Qiang, Y; Antony, J

2007-01-01

The crystal faceting planes and oxide coating structures of core-shell structured iron/iron-oxide nanoparticles synthesized by a sputter-gas-aggregation process were studied using transmission electron microscopy (TEM), electron diffraction and Wulff shape construction. The particles grown by this process and deposited on a support in a room temperature process have been compared with particles grown and deposited at high temperature as reported in the literature. It has been found that the Fe nanoparticles formed at RT are invariantly faceted on the {100} lattice planes and truncated by the {110} planes at different degrees. A substantial fraction of particles are confined only by the 6{100} planes (not truncated by the {110} planes); this contrasts with the Fe particles formed at high temperature (HT) for which a predominance of {110} planes has been reported. Furthermore, at RT no particle was identified to be only confined by the 12{110} planes, which is relatively common for the particles formed at HT. The Fe cubes defined by the 6{100} planes show a characteristic inward relaxation along the and directions and the reason for this behaviour is not fully understood. The oxide shell on the Fe{100} plane maintains an orientation relationship: Fe(001) parallel Fe 3 O 4 (001) and Fe[100] parallel Fe 3 O 4 [110], which is the same as the oxide formed on a bulk Fe(001) through thermal oxidation. Orientation of the oxide that forms on the Fe{110} facets differs from that on Fe{001}: therefore, properties of core-shell structured Fe nanoparticle faceted primarily with one type of lattice plane may be fully different from that faceted with another type of lattice plane

Hints of supernova debris deposition on the lunar surface: {sup 60}Fe and {sup 53}Mn measurements by means of accelerator mass spectrometry

Energy Technology Data Exchange (ETDEWEB)

Fimiani, Leticia; Faestermann, Thomas; Gomez Guzman, Jose Manuel; Hain, Karin; Korschinek, Gunther; Ludwig, Peter [Physik Department, Technische Universitaet Muenchen, Garching (Germany); Herzog, Gregory; Ligon, Bret; Park, Jisun [Department of Chemistry and Chemical Biology, Rutgers University, Piscataway, NJ (United States); Rugel, Georg [Forschungszentrum Dresden Rossendorf, Dresden (Germany)

2013-07-01

The enhanced concentration of {sup 60}Fe in a deep ocean ferro-manganese crust about (2.1±0.4) Myr old (Fitoussi et al., PRL 101, 121101 (2008)), suggests that one or more supernova (SN) explosions occurred in the vicinity of the Solar System. That observation was only possible with the ultra sensitive Accelerator Mass Spectrometry (AMS) technique at the Maier-Leibnitz-Laboratorium in Munich, where we are able to measure concentrations of {sup 60}Fe/Fe down to a level of 10{sup -16}. Because of its lacking atmosphere and negligible sedimentation rate, the Lunar surface is an excellent quantitative reservoir for SN debris. We searched for live {sup 60}Fe and {sup 53}Mn in samples from 3 Apollo missions. {sup 53}Mn is, similar as {sup 26}Al and {sup 60}Fe, a tool to trace nucleosynthesis activities. It is formed primarily during the explosive silicon-burning of the inner shells of SNe via {sup 53}Fe which β-decays to {sup 53}Mn with an 8.51 min half-life. Samples where we found an enhanced {sup 60}Fe concentration showed also an enhancement of {sup 53}Mn. If confirmed, this could be the first detection of live {sup 53}Mn originating from nucleosynthesis.

Correlated electron capture and inner-shell excitation measurements in ion-atom collisions

International Nuclear Information System (INIS)

Tanis, J.A.; Bernstein, E.M.; Clark, M.W.

1985-01-01

In an ion-atom collision projectile excitation and charge transfer (electron capture) may occur together in a single encounter. If the excitation and capture are correlated, then the process is called resonant transfer and excitation (RTE); if they are uncorrelated, then the process is termed nonresonant transfer and excitation (NTE). Experimental work to date has shown the existence of RTE and provided strong evidence for NTE. Results presented here provide information on the relative magnitudes of RTE and NTE, the charge state dependence of RTE, the effect of the target momentum distribution on RTE, the magnitude of L-shell RTE compared to K-shell RTE, and the target Z dependences of RTE and NTE. 15 refs., 5 figs

Faceted shell structure in grain boundary diffusion-processed sintered Nd–Fe–B magnets

International Nuclear Information System (INIS)

Seelam, U.M.R.; Ohkubo, T.; Abe, T.; Hirosawa, S.; Hono, K.

2014-01-01

Graphical abstract: The grain boundary diffusion process (GBDP) using a heavy rare earth elements (HRE) such as Dy and Tb is known as an effective method to enhance the coercivity of Nd–Fe–B sintered magnets without reducing remanence. This process has been industrially implemented to manufacture Nd–Fe–B based sintered magnets with high coercivity and high remanence. In this process, Dy is considered to diffuse through grain boundaries (GBs) to form (Nd 1−x Dy x ) 2 Fe 14 B shells surrounding the Nd 2 Fe 14 B grains and the higher anisotropy field of the Dy-rich shell is considered to suppress the nucleation of reverse domains at low magnetic field. Although there are several investigations on the microstructure of HRE GBDP Nd–Fe–B magnets, no paper addressed the origin of the asymmetric formation of HRE rich shells. Based on detailed analysis of facet planes of core/shell interfaces, we propose a mechanism of the faceted core/shell microstructure formation in the GBDP sintered magnets. We believe that this gives new insights on understanding the coercivity enhancement by the GBDP. - Highlights: • Faceting was observed at the interfaces of cores and shells. • The core/shell interfaces are sharp with an abrupt change in Dy concentration. • Meting occurs at the interfaces of metalic Nd-rich/Nd 2 Fe 14 B phases above 685 °C due to eutectic reaction. • Solidification of Dy-enriched liquid phase from 900 °C can result in the shell formation. - Abstract: Dysprosium enriched shell structure formed by the grain boundary diffusion process (GBDP) of a sintered Nd–Fe–B magnet was characterized by using scanning electron microscopy, electron back-scattered diffraction and transmission electron microscopy. Faceted core–shell interfaces with an abrupt change in Dy concentration suggest the Dy-rich shells are formed by the solidification of the liquid phase during cooling from the GBDP temperature. The Nd-rich phases are almost free from Dy, and

Synthesis and characterization of magnetically recyclable Ag nanoparticles immobilized on Fe3O4@C nanospheres with catalytic activity

International Nuclear Information System (INIS)

Li, Wei-hong; Yue, Xiu-ping; Guo, Chang-sheng; Lv, Jia-pei; Liu, Si-si; Zhang, Yuan; Xu, Jian

2015-01-01

Highlights: • Ag-loaded Fe 3 O 4 @C nanospheres were synthesized by a facile method. • The Fe 3 O 4 encapsulated mesoporous carbon was decorated with 10 nm Ag nanocrystals. • The as-prepared Ag-Fe 3 O 4 @C nanocomposite showed excellent catalytic activity. • The nanocomposite had convenient magnetic separability. - Abstract: A novel approach for the synthesis of Ag-loaded Fe 3 O 4 @C nanospheres (Ag-Fe 3 O 4 @C) was successfully developed. The catalysts possessed a carbon-coated magnetic core and grew active silver nanoparticles on the outer shell using hydrazine monohydrate as the AgNO 3 reductant in ethanol. The morphology, inner structure, and magnetic properties of the as-prepared composites were studied with transmission electron microscopy (TEM), X-ray powder diffraction (XRD), fourier translation infrared spectroscopy (FT-IR), and vibrating sample magnetometer (VSM) techniques. Catalytic activity was investigated by degrading rhodamine B (RhB) in the designed experiment. The obtained products were monodispersed and bifunctional with high magnetization, as well as exhibited excellent catalytic activity toward organic dye with 98% of RhB conversion within 20 min in the presence of NaBH 4 . The product also exhibited convenient magnetic separability and maintained high catalytic activity after six cycle runs

A novel Rapid Additive Manufacturing concept for architectural composite shell construction inspired by the shell formation in land snails.

Science.gov (United States)

Felbrich, Benjamin; Wulle, Frederik; Allgaier, Christoph; Menges, Achim; Verl, Alexander; Wurst, Karl-Heinz; Nebelsick, James

2018-01-04

State of the art rapid additive manufacturing (RAM), specifically Fused Filament Fabrication (FFF) has gained popularity among architects, engineers and designers for quick prototyping of technical devices, rapid production of small series and even construction scale fabrication of architectural elements. The spectrum of producible shapes and the resolution of detail, however, are determined and constrained by the layer-based nature of the fabrication process. These aspects significantly limit FFF-based approaches for the prefabrication and in-situ fabrication of freeform shells at the architectural scale. Snails exhibit a shell building process that suggests ways to overcome these limits. They produce a soft, pliable proteinaceous film - the periostracum - which later hardens and serves, among other functions, as a form-giving surface for an inner calcium carbonate layer. Snail shell formation behavior is interpreted from a technical point of view to extract potentially useful aspects for a biomimetic transfer. A RAM concept for continuous extrusion of thin free form composite shells inspired by the snail shell formation is presented. © 2018 IOP Publishing Ltd.

Core-shell magnetic nanowires fabrication and characterization

Energy Technology Data Exchange (ETDEWEB)

Kalska-Szostko, B., E-mail: kalska@uwb.edu.pl [Institute of Chemistry, University of Bialystok, Ciolkowskiego 1K, 15-245 Bialystok (Poland); Faculty of Physics, University of Bialystok, Ciolkowskiego 1L, 15-245 Bialystok, Poland (Poland); Klekotka, U.; Satuła, D. [Institute of Chemistry, University of Bialystok, Ciolkowskiego 1K, 15-245 Bialystok (Poland); Faculty of Physics, University of Bialystok, Ciolkowskiego 1L, 15-245 Bialystok, Poland (Poland)

2017-02-28

Highlights: • New approach for nanowires modification are presented. • Physical and chemical characterization of the nanowires are shown. • Properties modulations as an effect of the surface layer composition are discussed. - Abstract: In this paper, a new way of the preparation of core-shell magnetic nanowires has been proposed. For the modification Fe nanowires were prepared by electrodeposition in anodic aluminium oxide matrixes, in first step. In second, by wetting chemical deposition, shell layers of Ag, Au or Cu were obtained. Resultant core-shell nanowires structure was characterized by X-ray diffraction, infrared spectroscopy, transmission electron microscopy, and energy dispersive x-ray. Whereas magnetic properties by Mössbauer spectroscopy.

Anticavitation and Differential Growth in Elastic Shells

KAUST Repository

Moulton, Derek E.

2010-07-22

Elastic anticavitation is the phenomenon of a void in an elastic solid collapsing on itself. Under the action of mechanical loading alone typical materials do not admit anticavitation. We study the possibility of anticavitation as a consequence of an imposed differential growth. Working in the geometry of a spherical shell, we seek radial growth functions which cause the shell to deform to a solid sphere. It is shown, surprisingly, that most material models do not admit full anticavitation, even when infinite growth or resorption is imposed at the inner surface of the shell. However, void collapse can occur in a limiting sense when radial and circumferential growth are properly balanced. Growth functions which diverge or vanish at a point arise naturally in a cumulative growth process. © 2010 Springer Science+Business Media B.V.

Tissue distribution and developmental expression of type XVI collagen in the mouse.

Science.gov (United States)

Lai, C H; Chu, M L

1996-04-01

The expression of a recently identified collagen, alpha 1 (XVI), in adult mouse tissue and developing mouse embryo was examined by immunohistochemistry and in situ hybridization. A polyclonal antiserum was raised against a recombinant fusion protein, which contained a segment of 161 amino acids in the N-terminal noncollagenous domain of the human alpha 1 (XVI) collagen. Immunoprecipitation of metabolically labelled human or mouse fibroblast cell lysates with this antibody revealed a major, bacterial collagenase sensitive polypeptide of approximately 210 kDa. The size agrees with the prediction from the full-length cDNA. Immunofluorescence examination of adult mouse tissues using the affinity purified antibody revealed a rather broad distribution of the protein. The heart, kidney, intestine, ovary, testis, eye, arterial walls and smooth muscles all exhibited significant levels of expression, while the skeletal muscle, lung and brain showed very restricted and low signals. During development, no significant expression of the mRNA or protein was observed in embryo of day 8 of gestation, but strong signals was detected in placental trophoblasts. Expression in embryos was detectable first after day 11 of gestation with weak positive signals appearing in the heart. In later stages of development, stronger RNA hybridizations were observed in a variety of tissues, particularly in atrial and ventricular walls of the developing heart, spinal root neural fibers and skin. These data demonstrate that type XVI collagen represents another collagenous component widely distributed in the extracellular matrix and may contribute to the structural integrity of various tissues.

Simultaneous K plus L shell ionized atoms during heavy-ion ...

Indian Academy of Sciences (India)

The fraction of simultaneous K plus L shell ionized atoms is estimated in Fe, Co and Cu elements using carbon ions at different projectile energies. The present results indicate that the fraction of simultaneous K plus L shell ionization probability decreases with increase in projectile energy as well as with increase in the ...

The Whitish Inner Mantle of the Giant Clam, Tridacna squamosa, Expresses an Apical Plasma Membrane Ca2+-ATPase (PMCA Which Displays Light-Dependent Gene and Protein Expressions

Directory of Open Access Journals (Sweden)

Yuen K. Ip

2017-10-01

Full Text Available Giant clams live in symbiosis with extracellular zooxanthellae and display high rates of growth and shell formation (calcification in light. Light-enhanced calcification requires an increase in the supply of Ca2+ to, and simultaneously an augmented removal of H+ from, the extrapallial fluid where shell formation occurs. We have obtained the complete coding cDNA sequence of Plasma Membrane Ca2+-ATPase (PMCA from the thin and whitish inner mantle, which is in touch with the extrapallial fluid, of the giant clam Tridacna squamosa. The deduced PMCA sequence consisted of an apical targeting element. Immunofluorescence microscopy confirmed that PMCA had an apical localization in the shell-facing epithelium of the inner mantle, whereby it can actively secrete Ca2+ in exchange for H+. More importantly, the apical PMCA-immunofluorescence of the shell-facing epithelium of the inner mantle increased significantly after 12 h of exposure to light. The transcript and protein levels of PMCA/PMCA also increased significantly in the inner mantle after 6 or 12 h of light exposure. These results offer insights into a light-dependable mechanism of shell formation in T. squamosa and a novel explanation of light-enhanced calcification in general. As the inner mantle normally lacks light sensitive pigments, our results support a previous proposition that symbiotic zooxanthellae, particularly those in the colorful and extensible outer mantle, may act as light-sensing elements for the host clam.

Structural and magnetic properties of Fe-Al silica composites prepared by sequential ion implantation

International Nuclear Information System (INIS)

Julian Fernandez, C. de; Tagliente, M.A.; Mattei, G.; Sada, C.; Bello, V.; Maurizio, C.; Battaglin, G.; Sangregorio, C.; Gatteschi, D.; Tapfer, L.; Mazzoldi, P.

2004-01-01

The nanostructural and magnetic properties of Fe-Al/SiO 2 granular solids prepared by ion implantation have been investigated. A strong effect of the implantation order of the Fe and Al ions has been evidenced. By implanting first the Al ions and later Fe ions, 5-40 nm core-shell nanoparticles are formed with a magnetic behavior similar to that of Fe. The lattice parameter of the nanoparticles is consistent with that of the α-Fe. By changing the implantation order, 10-15 nm core-shell nanoparticles of a bcc Fe-based phase with a lattice 2.5% smaller than that of α-Fe are formed. The temperature dependence of the magnetization indicates a superparamagnetic behavior

Structural and magnetic properties of Fe-Al silica composites prepared by sequential ion implantation

Energy Technology Data Exchange (ETDEWEB)

Julian Fernandez, C. de E-mail: dejulian@padova.infm.it; Tagliente, M.A.; Mattei, G.; Sada, C.; Bello, V.; Maurizio, C.; Battaglin, G.; Sangregorio, C.; Gatteschi, D.; Tapfer, L.; Mazzoldi, P

2004-02-01

The nanostructural and magnetic properties of Fe-Al/SiO{sub 2} granular solids prepared by ion implantation have been investigated. A strong effect of the implantation order of the Fe and Al ions has been evidenced. By implanting first the Al ions and later Fe ions, 5-40 nm core-shell nanoparticles are formed with a magnetic behavior similar to that of Fe. The lattice parameter of the nanoparticles is consistent with that of the {alpha}-Fe. By changing the implantation order, 10-15 nm core-shell nanoparticles of a bcc Fe-based phase with a lattice 2.5% smaller than that of {alpha}-Fe are formed. The temperature dependence of the magnetization indicates a superparamagnetic behavior.

Single and multi-layered core-shell structures based on ZnO nanorods obtained by aerosol assisted chemical vapor deposition

Energy Technology Data Exchange (ETDEWEB)

Sáenz-Trevizo, A.; Amézaga-Madrid, P.; Pizá-Ruiz, P.; Antúnez-Flores, W.; Ornelas-Gutiérrez, C.; Miki-Yoshida, M., E-mail: mario.miki@cimav.edu.mx

2015-07-15

Core–shell nanorod structures were prepared by a sequential synthesis using an aerosol assisted chemical vapor deposition technique. Several samples consisting of ZnO nanorods were initially grown over TiO{sub 2} film-coated borosilicate glass substrates, following the synthesis conditions reported elsewhere. Later on, a uniform layer consisting of individual Al, Ni, Ti or Fe oxides was grown onto ZnO nanorod samples forming the so-called single MO{sub x}/ZnO nanorod core–shell structures, where MO{sub x} was the metal oxide shell. Additionally, a three-layer core–shell sample was developed by growing Fe, Ti and Fe oxides alternately, onto the ZnO nanorods. The microstructure of the core–shell materials was characterized by grazing incidence X-ray diffraction, scanning and transmission electron microscopy. Energy dispersive X-ray spectroscopy was employed to corroborate the formation of different metal oxides. X-ray diffraction outcomes for single core–shell structures showed solely the presence of ZnO as wurtzite and TiO{sub 2} as anatase. For the multi-layered shell sample, the existence of Fe{sub 2}O{sub 3} as hematite was also detected. Morphological observations suggested the existence of an outer material grown onto the nanorods and further microstructural analysis by HR-STEM confirmed the development of core–shell structures in all cases. These studies also showed that the individual Al, Fe, Ni and Ti oxide layers are amorphous; an observation that matched with X-ray diffraction analysis where no apparent extra oxides were detected. For the multi-layered sample, the development of a shell consisting of three different oxide layers onto the nanorods was found. Overall results showed that no alteration in the primary ZnO core was produced during the growth of the shells, indicating that the deposition technique used herein was and it is suitable for the synthesis of homogeneous and complex nanomaterials high in quality and purity. In addition

Ultraefficient separation and sensing of mercury and methylmercury ions in drinking water by using aminonaphthalimide-functionalized Fe(3)O(4)@SiO(2) core/shell magnetic nanoparticles.

Science.gov (United States)

Park, Minsung; Seo, Sungmin; Lee, In Su; Jung, Jong Hwa

2010-07-07

A new fluorogenic based aminonaphthalimide-functionalized Fe(3)O(4)@SiO(2) core/shell magnetic nanoparticles 1 has been prepared, and its abilities to sense and separate metal ions were evaluated by fluorophotometry. The nanoparticles 1 exhibited a high affinity and selectivity for Hg(2+) and CH(3)Hg(+) ions over competing metal ions.

Improvement in the reliability of shells for light water reactors by manufacture from hollow ingots

International Nuclear Information System (INIS)

Bocquet, P.; Blondeau, R.; Poitrault, I.; Badeau, J.P.; Dumont, R.

1991-01-01

The problems associated to the segregation located at the inner surface and subsurface of heavy shell forgings used in nuclear light water reactors are presented. The effect of A segregation on cold or reheat cracking HAZ has conducted fabricators to use severe welding procedures with high preheat temperature and refining HAZ grain size sequences. For shells and rings, the hollow ingot as developed by CLI, with a good control of the location of the center line of segregation, is an excellent answer to these problems. The use of core shell forgings issued from this type of hollow ingots, free of segregation at the inner surface and subsurface area, contributes, by reducing the irradiation embrittlement effect, to increase the safety factor relatively to the risk of failure of the reactor. (orig.)

(3He,α) reaction mechanism at high energy and neutron inner shell structure

International Nuclear Information System (INIS)

Wiele, J. van de.

1980-01-01

The ( 3 He,α) reaction on 12 C, 16 O, 28 Si, 58 Ni, 90 Zr, 118 Sn, 124 Sn and 208 Pb targets has been studied at Esub( 3 He) = 217 MeV (or 205 MeV) in order to investigate the reaction mechanism at high energy and large momentum transfer. The reaction yields large cross sections at very forward angles and strongly enhances the largest orbital momentum transfer. The angular distribution shapes are well reproduced in the frame-work of the Z-R- D.W.B.A. analysis if we use a unique empirical α-potential: Vsub(α)(Esub(α)) = Vsub( 3 He)(3/4 Esub(α)) + Vsub(n)(1/4 Esub(α)). The excitation energy spectra have been measured up to 100 MeV in the residual light and medium nuclei and up to about 16 MeV in heavy nuclei. In addition to the well-known low-lying levels, peaks or broad structures are observed for each nucleus at higher excitation energies. They are attributed to pick up from inner shells: 1s( 11 C and 15 O), 1p( 27 Si), 1d5/2 + 1p( 57 Ni), 1f7/2( 89 Zr) 1g9/2 117 Sn, 123 Sn and 1h11/2( 207 Pb). Selectivity and localization of direct and indirect pick up ( 3 He,α) reactions were studied. Finite range calculations show that this reaction is not very sensitive to the details of the range from function but only to D 0 coefficient and range R. A microscopic α-nucleus optical potential calculated with n-n dependent and independent density forces is able to reproduce both elastic scattering and pick up reaction angular distributions [fr

Thermal annealing dynamics of carbon-coated LiFePO{sub 4} nanoparticles studied by in-situ analysis

Energy Technology Data Exchange (ETDEWEB)

Krumeich, Frank, E-mail: krumeich@inorg.chem.ethz.ch [Department of Chemistry and Applied Biosciences, ETH Zurich, Vladimir-Prelog-Weg 1, 8093 Zurich (Switzerland); Waser, Oliver; Pratsinis, Sotiris E. [Department of Mechanical and Process Engineering, ETH Zurich, Sonneggstrasse 3, 8092 Zurich (Switzerland)

2016-10-15

The thermal behavior of core-shell carbon-coated lithium iron phosphate (LiFePO{sub 4}-C) nanoparticles made by flame spray pyrolysis (FSP) during annealing was investigated by in-situ transmission electron microscopy (TEM), in-situ X-ray powder diffraction (XRD) as well as ex-situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). Crystallization of the initially glassy LiFePO{sub 4}-C nanoparticles starts at quite low temperatures (T=400 °C), forming single crystals inside the confinement of the carbon shell. Upon increasing the temperature to T≥700 °C, LiFePO{sub 4} starts to diffuse through the carbon shell resulting in cavities inside the mostly intact carbon shell. By increasing the temperature further to T≥800 °C, the initial core-shell morphology converts into open carbon shells (flakes and cenospheres) and bulky LiFePO{sub 4} particles (diameter in the range 300–400 nm), in agreement with ex-situ experiments. - Graphical abstract: TEM images of a typical sample area recorded at room temperature and after heating in-situ heating reveal the growth of particles and the formation of empty carbon cages. - Highlights: • LiFePO{sub 4} coated by a carbon shell is produced by flame spray pyrolysis. • The amorphous LiFePO{sub 4} starts to crystallize at 400 °C as revealed by in-situ XRD. • Crystal growth was visualized by TEM heating experiments. • The formation of empty carbon cages starts at 700 °C.

Synthesis, characterization and electromagnetic properties of SnO-coated FeNi alloy nanocapsules

Energy Technology Data Exchange (ETDEWEB)

Li, Mingling; Li, Honglin; Xu, Taotao; Nie, Yu, E-mail: lml771212@163.com [College of Chemistry and Material Engineering, Chaohu University (China)

2016-11-15

SnO-coated FeNi alloy nanocapsules have been synthesized by an arc-discharge method. High resolution transmission electron microscopy and x-ray photoelectron spectroscopy analysis show that the nanocapsules have a shell/core structure with FeNi alloy nanoparticles as the core and amorphous SnO as the shell. Dielectric relaxation of SnO shell and the interfacial relaxation between SnO shell and FeNi core lead to the dual nonlinear dielectric resonance. The natural resonance in the SnO coated FeNi nanocapsules shifts to 14.0 GHz. Reflection loss (RL) reaches -46.1 dB at 14.8 GHz for a matching thickness of 1.95 mm, while it exceeds-20 dB over the 13.6 -16.7 GHz range and it exceeds -10 dB in the whole Ku-band (12.4-18 GHz). In addition, the optimal RL values at 5.0-7.6 GHz with the absorbing thickness of 3.4-5.0 mm just exhibit a slight fluctuation. (author)

Ultrahigh coercivity and core-shell microstructure achieved in oriented Nd-Fe-B thin films diffusion-processed with Dy-based alloys

Energy Technology Data Exchange (ETDEWEB)

Zhang, Tongbo; Zhou, Xiaoqian; Yu, Dedong; Fu, Yanqing; Cui, Weibin [Northeastern University, Key Laboratory of Electromagnetic Processing of Materials (EPM), Ministry of Education, Shenyang (China); Northeastern University, Department of Physics and Chemistry of Materials, School of Materials Science and Engineering, Shenyang (China); Li, Guojian; Wang, Qiang [Northeastern University, Key Laboratory of Electromagnetic Processing of Materials (EPM), Ministry of Education, Shenyang (China)

2017-01-15

Ultrahigh ambient coercivities of ∝4 T were achieved in Nd-Fe-B benchmark thin film with coercivity of 1.06 T by diffusion-processing with Dy, Dy{sub 70}Cu{sub 30} and Dy{sub 80}Ag{sub 20} alloy layer. High texture and good squareness were obtained. In triple-junction regions, Dy element was found to be immiscible with Nd element. Microstructure observation indicated the typical gradient elementary distribution. Unambiguous core/shell microstructure was characterized by transition electron microscopy. Due to the enhanced ambient coercivity, the coercivity temperature stability was also substantially increased. (orig.)

High-resolution Laboratory Measurements of Coronal Lines near the Fe IX Line at 171 Å

Science.gov (United States)

Beiersdorfer, Peter; Träbert, Elmar

2018-02-01

We present high-resolution laboratory measurements in the spectral region between 165 and 175 Å that focus on the emission from various ions of C, O, F, Ne, S, Ar, Fe, and Ni. This wavelength region is centered on the λ171 Fe IX channel of the Atmospheric Imaging Assembly on the Solar Dynamics Observatory, and we place special emphasis on the weaker emission lines of Fe IX predicted in this region. In general, our measurements show a multitude of weak lines missing in the current databases, where the emission lines of Ni are probably most in need of further identification and reclassification. We also find that the wavelengths of some of the known lines need updating. Using the multi-reference Møller–Plesset method for wavelength predictions and collisional-radiative modeling of the line intensities, we have made tentative assignments of more than a dozen lines to the spectrum of Fe IX, some of which have formerly been identified as Fe VII, Fe XIV, or Fe XVI lines. Several Fe features remain unassigned, although they appear to be either Fe VII or Fe X lines. Further work will be needed to complete and correct the spectral line lists in this wavelength region.

Photoionization of the Fe lons: Structure of the K-Edge

Science.gov (United States)

Palmeri, P.; Mendoza, C.; Kallman, T.; Bautista, M.; White, Nicholas E. (Technical Monitor)

2002-01-01

X-ray absorption and emission features arising from the inner-shell transitions in iron are of practical importance in astrophysics due to the Fe cosmic abundance and to the absence of traits from other elements in the nearby spectrum. As a result, the strengths and energies of such features can constrain the ionization stage, elemental abundance, and column density of the gas in the vicinity of the exotic cosmic objects, e.g. active galactic nuclei (AGN) and galactic black hole candidates. Although the observational technology in X-ray astronomy is still evolving and currently lacks high spectroscopic resolution, the astrophysical models have been based on atomic calculations that predict a sudden and high step-like increase of the cross section at the K-shell threshold (see for instance. New Breit-Pauli R-matrix calculations of the photoionization cross section of the ground states of Fe XVII in the region near the K threshold are presented. They strongly support the view that the previously assumed sharp edge behaviour is not correct. The latter has been caused by the neglect of spectator Auger channels in the decay of the resonances converging to the K threshold. These decay channels include the dominant KLL channels and give rise to constant widths (independent of n). As a consequence, these series display damped Lorentzian components that rapidly blend to impose continuity at threshold, thus reformatting the previously held picture of the edge. Apparent broadened iron edges detected in the spectra of AGN and galactic black hole candidates seem to indicate that these quantum effects may be at least partially responsible for the observed broadening.

The microwave properties of composites including lightweight core–shell ellipsoids

International Nuclear Information System (INIS)

Yuan, Liming; Xu, Yonggang; Dai, Fei; Liao, Yi; Zhang, Deyuan

2016-01-01

In order to study the microwave properties of suspensions including lightweight core–shell ellipsoids, the calculation formula was obtained by substituting an equivalent ellipsoid for the original core–shell ellipsoid. Simulations for Fe-coated diatomite/paraffin suspensions were performed. Results reveal that the calculated results fitted the measured results very well when the inclusion concentration was no more than 15 vol%, but there was an obvious deviation when the inclusion concentration reached 24 vol%. By comparisons, the formula for less diluted suspensions was more suitable for calculating the electromagnetic parameter of suspensions especially when the ratio was smaller between the electromagnetic parameter of the inclusion and that of the host medium. - Highlights: • The microwave properties of suspensions with core-shell inclusions were studied. • Less diluted suspensions were considered. • Flaky Fe-coated diatomite/paraffin suspensions were studied. • The microwave properties could be simulated successfully.

The microwave properties of composites including lightweight core–shell ellipsoids

Energy Technology Data Exchange (ETDEWEB)

Yuan, Liming, E-mail: lming_y@163.com [Science and Technology on Electromagnetic Scattering Laboratory, Shanghai 200438 (China); Xu, Yonggang; Dai, Fei; Liao, Yi [Science and Technology on Electromagnetic Scattering Laboratory, Shanghai 200438 (China); Zhang, Deyuan [School of Mechanical Engineering and Automation, Beihang University, Beijing 100191 (China)

2016-12-01

In order to study the microwave properties of suspensions including lightweight core–shell ellipsoids, the calculation formula was obtained by substituting an equivalent ellipsoid for the original core–shell ellipsoid. Simulations for Fe-coated diatomite/paraffin suspensions were performed. Results reveal that the calculated results fitted the measured results very well when the inclusion concentration was no more than 15 vol%, but there was an obvious deviation when the inclusion concentration reached 24 vol%. By comparisons, the formula for less diluted suspensions was more suitable for calculating the electromagnetic parameter of suspensions especially when the ratio was smaller between the electromagnetic parameter of the inclusion and that of the host medium. - Highlights: • The microwave properties of suspensions with core-shell inclusions were studied. • Less diluted suspensions were considered. • Flaky Fe-coated diatomite/paraffin suspensions were studied. • The microwave properties could be simulated successfully.

Preparation of Fe(3)O(4)@C@CNC multifunctional magnetic core/shell nanoparticles and their application in a signal-type flow-injection photoluminescence immunosensor.

Science.gov (United States)

Chu, Chengchao; Li, Meng; Li, Long; Ge, Shenguang; Ge, Lei; Yu, Jinghua; Yan, Mei; Song, Xianrang

2013-11-01

We describe here the preparation of carbon-coated Fe3O4 magnetic nanoparticles that were further fabricated into multifunctional core/shell nanoparticles (Fe3O4@C@CNCs) through a layer-by-layer self-assembly process of carbon nanocrystals (CNCs). The nanoparticles were applied in a photoluminescence (PL) immunosensor to detect the carcinoembryonic antigen (CEA), and CEA primary antibody was immobilized onto the surface of the nanoparticles. In addition, CEA secondary antibody and glucose oxidase were covalently bonded to silica nanoparticles. After stepwise immunoreactions, the immunoreagent was injected into the PL cell using a flow-injection PL system. When glucose was injected, hydrogen peroxide was obtained because of glucose oxidase catalysis and quenched the PL of the Fe3O4@C@CNC nanoparticles. The here proposed PL immunosensor allowed us to determine CEA concentrations in the 0.005–50 ng·mL-1 concentration range, with a detection limit of 1.8 pg·mL-1.

Pearl-necklace structures in core-shell molecular brushes: Experiments, Monte Carlo simulations and self-consistent field modeling

NARCIS (Netherlands)

Polotsky, A.; Charlaganov, M.; Xu, Y.P.; Leermakers, F.A.M.; Daoud, M.; Muller, A.H.E.; Dotera, T.; Borisov, O.V.

2008-01-01

We present theoretical arguments and experimental evidence for a longitudinal instability in core-shell cylindrical polymer brushes with a solvophobic inner (core) block and a solvophilic outer (shell) block in selective solvents. The two-gradient self-consistent field Scheutjens-Fleer (SCF-SF)

Control of the Speed of a Light-Induced Spin Transition through Mesoscale Core-Shell Architecture.

Science.gov (United States)

Felts, Ashley C; Slimani, Ahmed; Cain, John M; Andrus, Matthew J; Ahir, Akhil R; Abboud, Khalil A; Meisel, Mark W; Boukheddaden, Kamel; Talham, Daniel R

2018-05-02

The rate of the light-induced spin transition in a coordination polymer network solid dramatically increases when included as the core in mesoscale core-shell particles. A series of photomagnetic coordination polymer core-shell heterostructures, based on the light-switchable Rb a Co b [Fe(CN) 6 ] c · mH 2 O (RbCoFe-PBA) as core with the isostructural K j Ni k [Cr(CN) 6 ] l · nH 2 O (KNiCr-PBA) as shell, are studied using temperature-dependent powder X-ray diffraction and SQUID magnetometry. The core RbCoFe-PBA exhibits a charge transfer-induced spin transition (CTIST), which can be thermally and optically induced. When coupled to the shell, the rate of the optically induced transition from low spin to high spin increases. Isothermal relaxation from the optically induced high spin state of the core back to the low spin state and activation energies associated with the transition between these states were measured. The presence of a shell decreases the activation energy, which is associated with the elastic properties of the core. Numerical simulations using an electro-elastic model for the spin transition in core-shell particles supports the findings, demonstrating how coupling of the core to the shell changes the elastic properties of the system. The ability to tune the rate of optically induced magnetic and structural phase transitions through control of mesoscale architecture presents a new approach to the development of photoswitchable materials with tailored properties.

Sustainable solid-state strategy to hierarchical core-shell structured Fe 3 O 4 @graphene towards a safer and green sodium ion full battery

KAUST Repository

Ding, Xiang

2017-12-11

A sustainable solid-state strategy of SPEX milling is developed to coat metal oxide (e.g., Fe3O4) with tunable layers of graphene, and a new hierarchical core-shell structured Fe3O4@graphene composite is constructed. The presented green process can preserve the physicochemical properties of metal (oxide) nanocrystals well while conveniently modifying them with graphene carbon, which is unique from the conventional approaches carried out in the solution followed by high temperature calcinations/carbonization. This strategy is environmental-friendly, cost-effective and feasible to extend for preparing more metal (oxide)-graphene materials readily with controllable layers of graphene. In energy storage applications, as-prepared Fe3O4@graphene only modified with 10 wt% of graphene can show greater capacity of 283 mAh g−1 at 100 mA g−1 with capacity retention of 84% over 100 cycles in sodium battery (vs. 17% of pristine Fe3O4). As an appealing nonflammable anode, a completely new full battery of Fe3O4@graphite/Na2.4Fe1.8(SO4)3 is assembled, and an impressive energy density beyond 300 Wh kgcathode−1 with a high working voltage of 3.2 V is attained. Such kind of green battery comprising from the earth-abundant elements (i.e., Na, Fe, S and O) can demonstrate extremely long cycle ability over 500 cycles and robust rate capability even to 10 C (where 1 C define as 108 mA gcathode−1) which are rarely reported before.

Modeling the carbon isotope composition of bivalve shells (Invited)

Science.gov (United States)

Romanek, C.

2010-12-01

The stable carbon isotope composition of bivalve shells is a valuable archive of paleobiological and paleoenvironmental information. Previous work has shown that the carbon isotope composition of the shell is related to the carbon isotope composition of dissolved inorganic carbon (DIC) in the ambient water in which a bivalve lives, as well as metabolic carbon derived from bivalve respiration. The contribution of metabolic carbon varies among organisms, but it is generally thought to be relatively low (e.g., 90%) in the shells from terrestrial organisms. Because metabolic carbon contains significantly more C-12 than DIC, negative excursions from the expected environmental (DIC) signal are interpreted to reflect an increased contribution of metabolic carbon in the shell. This observation contrasts sharply with modeled carbon isotope compositions for shell layers deposited from the inner extrapallial fluid (EPF). Previous studies have shown that growth lines within the inner shell layer of bivalves are produced during periods of anaerobiosis when acidic metabolic byproducts (e.g., succinic acid) are neutralized (or buffered) by shell dissolution. This requires the pH of EPF to decrease below ambient levels (~7.5) until a state of undersaturation is achieved that promotes shell dissolution. This condition may occur when aquatic bivalves are subjected to external stressors originating from ecological (predation) or environmental (exposure to atm; low dissolved oxygen; contaminant release) pressures; normal physiological processes will restore the pH of EPF when the pressure is removed. As a consequence of this process, a temporal window should also exist in EPF at relatively low pH where shell carbonate is deposited at a reduced saturation state and precipitation rate. For example, EPF chemistry should remain slightly supersaturated with respect to aragonite given a drop of one pH unit (6.5), but under closed conditions, equilibrium carbon isotope fractionation

Subshell resolved L shell ionization of Bi and U induced by 16 - 45 keV electrons

International Nuclear Information System (INIS)

Rahangdale, Hitesh; Das, Pradipta K.; Saha, S.; Mitra, D.

2015-01-01

Electron induced inner-shell ionization is important for both fundamental and applied research. Ionization of outer atomic energy levels has been studied extensively than for inner levels. Knowledge of inner shell ionization cross sections is important in X-ray and Auger electron spectroscopy and in the fields of astrophysics, plasma physics, surface science and many more. At electron impact energies near the atomic binding energies the distortion of the wave functions from plane wave towards a spherical wave, due to the electrostatic field of the atoms, needs to be considered. The distorted wave Born approximation (DWBA) calculations, taking relativistic effects and exchange interaction into account, is used to estimate the K, L and M-shell ionization cross-section for the atoms. Earlier experiments on electron impact ionization studies focused mainly on K-shell ionization cross-section, while L and M-shell ionization data were hardly reported. A review of the existing L-shell ionization cross-section data shows that, while the X-ray production cross-sections by electron impact were reported quite a few times, the reporting of subshell resolved ionization cross-sections were rarely found near the ionization threshold region. In the present work, we have measured the X ray production cross-sections of different L lines of Bi and U induced by 16-45 keV electrons and converted the obtained values to the subshell specific ionization cross-sections. The experimental data are compared with the theoretical calculations based on the (DWBA) obtained from PENELOPE. To the best of our knowledge, the subshell resolved electron induced ionization cross-sections for the L-shell of Bi and U are reported here for the first time at the energy values near the corresponding ionization threshold. (author)

Double-shell target fabrication workshop-2016 report

Energy Technology Data Exchange (ETDEWEB)

Wang, Y. Morris [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Oertel, John [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Farrell, Michael [General Atomics, San Diego, CA (United States); Baumann, Ted [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Huang, Haibo [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Nikroo, Abbas [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2017-01-10

On June 30, 2016, over 40 representatives from Lawrence Livermore National Laboratory (LLNL), Los Alamos National Laboratory (LANL), General Atomics (GA), Laboratory for Laser Energetics (LLE), Schafer Corporation, and NNSA headquarter attended a double-shell (DS) target fabrication workshop at Livermore, California. Pushered-single-shell (PSS) and DS metalgas platforms potentially have a large impact on programmatic applications. The goal of this focused workshop is to bring together target fabrication scientists, physicists, and designers to brainstorm future PSS and DS target fabrication needs and strategies. This one-day workshop intends to give an overall view of historical information, recent approaches, and future research activities at each participating organization. Five topical areas have been discussed that are vital to the success of future DS target fabrications, including inner metal shells, foam spheres, outer ablators, fill tube assembly, and metrology.

EDITORIAL: XVI Brazilian Colloquium on Orbital Dynamics

Science.gov (United States)

de Melo, Cristiano F.; Macau, Elbert E. N.; Prado, Antonio B. A.; Hetem Jnr, Annibal

2013-10-01

The XVI Brazilian Colloquium on Orbital Dynamics was held from 26-30 November 2012, at the Biazi Grand Hotel, Serra Negra, São Paulo, Brazil. The Brazilian Colloquia on Orbital Dynamics are scientific events that occur bi-annually and are designed to develop those areas of research in celestial mechanics, orbital dynamics, planetary science, fundamental astronomy, aerospace engineering, and nonlinear systems and chaos. The meeting has been held for 30 years and it brings together researchers, professors and students from South American and also from other continents. Acknowledgements National Council for Scientific and Technological Development - CNPq Coordination for the Improvement of Higher Level - CAPES São Paulo Research Foundation - FAPESP

Synthesis, structure and magnetic properties of Fe-Gd nanocapsules coated with B2O3/H3BO3 and Fe3BO5+GdBO3

International Nuclear Information System (INIS)

Si, P.Z.; Brueck, E.; Zhang, Z.D.; Tegus, O.; Buschow, K.H.J.; Zhang, W.S.; Klaasse, J.C.P.; Boer, F.R. de

2004-01-01

Nanocapsules consisting of B 2 O 3 /H 3 BO 3 encapsulating Fe-Gd cores have been synthesized by an arc-discharge process using metal-boron alloys as cathode. Most of the nanocapsules have a well-constructed shell/core structure with a uniform B 2 O 3 /H 3 BO 3 shell. Heat-treatment induces reactions between the shell and the core, resulting in the formation of a Fe 3 BO 5 +GdBO 3 matrix embedded with Fe nanoparticles, reduction of the metallic-core size and decrease of the blocking temperature T B . Above T B , the magnetization curves plotted vs. H/T overlap and show zero coercivity. Below T B , the coercivity shows a linear dependence when plotted vs. T 1/2 . However, the coercivity-T 1/2 curve below 60 K has a different slope from that above 60 K, indicating the existence of two different magnetic phases in the nanocapsules. Different from bulk Fe 3 BO 5 , nanoscale Fe 3 BO 5 particles have a lower transition temperature to the weak-ferromagnetic state, and magnetic hysteresis is absent due to size effects

Faceted shell structure in grain boundary diffusion-processed sintered Nd–Fe–B magnets

Energy Technology Data Exchange (ETDEWEB)

Seelam, U.M.R.; Ohkubo, T.; Abe, T.; Hirosawa, S.; Hono, K., E-mail: kazuhiro.hono@nims.go.jp

2014-12-25

Graphical abstract: The grain boundary diffusion process (GBDP) using a heavy rare earth elements (HRE) such as Dy and Tb is known as an effective method to enhance the coercivity of Nd–Fe–B sintered magnets without reducing remanence. This process has been industrially implemented to manufacture Nd–Fe–B based sintered magnets with high coercivity and high remanence. In this process, Dy is considered to diffuse through grain boundaries (GBs) to form (Nd{sub 1−x}Dy{sub x}){sub 2}Fe{sub 14}B shells surrounding the Nd{sub 2}Fe{sub 14}B grains and the higher anisotropy field of the Dy-rich shell is considered to suppress the nucleation of reverse domains at low magnetic field. Although there are several investigations on the microstructure of HRE GBDP Nd–Fe–B magnets, no paper addressed the origin of the asymmetric formation of HRE rich shells. Based on detailed analysis of facet planes of core/shell interfaces, we propose a mechanism of the faceted core/shell microstructure formation in the GBDP sintered magnets. We believe that this gives new insights on understanding the coercivity enhancement by the GBDP. - Highlights: • Faceting was observed at the interfaces of cores and shells. • The core/shell interfaces are sharp with an abrupt change in Dy concentration. • Meting occurs at the interfaces of metalic Nd-rich/Nd{sub 2}Fe{sub 14}B phases above 685 °C due to eutectic reaction. • Solidification of Dy-enriched liquid phase from 900 °C can result in the shell formation. - Abstract: Dysprosium enriched shell structure formed by the grain boundary diffusion process (GBDP) of a sintered Nd–Fe–B magnet was characterized by using scanning electron microscopy, electron back-scattered diffraction and transmission electron microscopy. Faceted core–shell interfaces with an abrupt change in Dy concentration suggest the Dy-rich shells are formed by the solidification of the liquid phase during cooling from the GBDP temperature. The Nd-rich phases

Core-shell structure of Miglyol/poly(D,L-lactide)/Poloxamer nanocapsules studied by small-angle neutron scattering.

Science.gov (United States)

Rübe, Andrea; Hause, Gerd; Mäder, Karsten; Kohlbrecher, Joachim

2005-10-03

The contrast variation technique in small angle neutron scattering (SANS) was used to investigate the inner structure of nanocapsules on the example of poly(D,L-lactide) (PLA) nanocapsules. The determination of the PLA and Poloxamer shell thickness was the focus of this study. Highest sensitivity on the inner structure of the nanocapsules was obtained when the scattering length density of the solvent was varied between the one of the Miglyol core and the PLA shell. According to the fit data the PLA shell thickness was 9.8 nm. The z-averaged radius determined by SANS experiments correlated well with dynamic light scattering (DLS) results, although DLS values were systematically slightly higher than the ones measured by SANS. This could be explained by taking into account the influence of Poloxamer attached to the nanocapsules surface. For a refined fit model with a second shell consisting of Poloxamer, SANS values and DLS values fitted well with each other. The characterization method presented here is significant because detailed insights into the nanocapsule and the Poloxamer shell were gained for the first time. This method could be used to develop strategies for the optimization of the shell properties concerning controlled release and to study changes in the shell structure during degradation processes.

Ag-decorated Fe_3O_4@SiO_2 core-shell nanospheres: Seed-mediated growth preparation and their antibacterial activity during the consecutive recycling

International Nuclear Information System (INIS)

Li, Miaomiao; Wu, Wenjie; Qiao, Ru; Tan, Linxiang; Li, Zhengquan; Zhang, Yong

2016-01-01

We demonstrated a seed-mediated growth approach to synthesize Ag nanoparticles-decorated Fe_3O_4@SiO_2 core-shell nanospheres without use of surface functionalization. The particle size and decoration density of the immobilized Ag nanoparticles on SiO_2 surface were tunable by adjusting the added AgNO_3 concentration and the alternating repetition times in seed-mediated growth procedure. The as-prepared Ag-decorated Fe_3O_4@SiO_2 nanospheres exhibited excellent antibacterial activities against Escherichia coli, Bacillus subtilis and Candida albicans, in which the minimum inhibitory concentration were 12.5 μg mL"−"1, 50 μg mL"−"1 and 50 μg mL"−"1, respectively. It is speculated that their antibacterial activity is attributed to both the interaction of released Ag ions with the functional groups of vital enzymes and proteins and the strong oxidation of reactive oxygen species generated under the action of photoinduced electrons in Ag nanoparticles. Besides studying their antibacterial mechanism, we also investigated the variation of antibacterial activity of these heterostructured nanospheres during the consecutive magnetic separation and recycling. It shows that the magnetic antibacterial agent could be reused and its activity remained stable even after nine cycles, which enable it to be promisingly applied in biomedical areas. - Highlights: • Ag-decorated Fe_3O_4@SiO_2 were synthesized via a seed-mediated growth method. • The core-shell heterostructures exhibited excellent antibacterial activity. • The activity was attributed to the effect of released Ag"+ with ROS oxidation. • The antibacterial agent was reused during magnetic separation and recycling.

Taki onqoy: epidemia de intoxicación por exposición al mercurio en Huamanga del siglo XVI

Directory of Open Access Journals (Sweden)

Luis Alberto Santa María

Full Text Available Taki Onqoy es un síndrome que corresponde a la intoxicación por exposición al mercurio. Apareció como consecuencia de la explotación de las minas de mercurio de Paras y Huancavelica en el Perú durante el siglo XVI. La caquexia mercurial, última etapa de la enfermedad, estaría asociada a la idea del pishtaco. El Taki Onqoy en el Perú del siglo XVI, representa la mayor epidemia por intoxicación por mercurio conocida por la humanidad.

Plantas medicinais consumidas em Cochim, no século XVI e na atualidade

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Isabel Maria Madaleno

Full Text Available O objetivo primacial desta pesquisa é investigar como solucionam os habitantes de Cochim, na Índia, seus problemas de saúde, quando não podem aceder aos sistemas convencionais ou quando optam por aceder a sistemas alternativos, na modernidade. O objetivo específico da pesquisa é compilar as espécies vegetais de uso terapêutico no século XVI e compará-las com as atuais. A flora indiana, em particular as especiarias, tem fascinado a humanidade desde o início dos tempos. Em 1498, os portugueses descobriram o caminho marítimo para a Índia e, durante os dois séculos seguintes, o pequeno país europeu dominou o comércio mundial com o oriente. Seguindo a rota das especiarias, o Instituto de Investigação Científica Tropical (IICT organizou, recentemente, uma missão científica a Kerala, a fim de investigar os frutos, os legumes, os condimentos, os tubérculos e as plantas medicinais cultivadas em jardins e pátios traseiros, vendidos em mercados e feiras, e recomendados pela medicina Ayurvédica, na cidade de Cochim. O ponto de partida foi a leitura de quatro manuscritos do século XVI que enumeravam as plantas aromáticas, condimentares e medicinais da Índia renascentista. Os resultados demonstram que um número substancial de plantas colhidas durante a missão do IICT, em 2013, já era usado na Índia, no século XVI.

THE XVI. CENTURY POET SHERÎFÎ’S WORK CALLED SHEVÂHİDÜ’SH-SHÜHEDÂ / XVI. ASIR SAİRLERİNDEN EĞİRDİRLİ SERÎFÎ’NİN SEVÂHİDÜ’S-SÜHEDÂ’SI

Directory of Open Access Journals (Sweden)

Dr. Sadık YAZAR

2009-04-01

Full Text Available In this article, which XVI. century poet Sherîfî’swork called Shevâhidü’sh-shühedâ, that can be a newexample of the maktel (elegy genre, was presented; firstlyI gave brief information about Serîfî and his works. I alsolooked at the maktel (elegy genre’s development and itsexamples in the classical Turkish literature –formbegining to end of the XVI. century- briefly. In the last part of the artcile I compared Sherîfî’s Shevâhidü’shshühedâwith the Fuzûlî’s –the famous XVI. centuryTurkish poet- Hadîqatü’s-sü’edâ and after this compare itwas understood that Sherîfî has benefited from Fuzûlî’swork at the degree of plagiarism. After all these, it wasunderstood that Sherîfî’s Shevâhidü’sh-shühedâ has nomuch value of the originalty.

Theoretical analysis and numerical simulation of electromagnetic parameters of Fe-C coaxial single fiber

Energy Technology Data Exchange (ETDEWEB)

Xie, Wei, E-mail: cslggncl@163.com [Key Laboratory of Safety Design and Reliability Technology for Engineering Vehicle, Hunan Province, Changsha University of Science and Technology, Changsha 410114 (China); Hunan Province Higher Education Key Laboratory of Modeling and Monitoring on the Near-Earth Electromagnetic Environments, Changsha University of Science & Technology, Changsha 410114 (China); College of Aerospace Science and Engineering, National University of Defense Technology, Changsha 410073 (China); Chemical and Biomolecular Engineering Department, University of Tennessee, Knoxville, TN 37996 (United States); Zhu, Xukun; Kuang, Jiacai [Key Laboratory of Safety Design and Reliability Technology for Engineering Vehicle, Hunan Province, Changsha University of Science and Technology, Changsha 410114 (China); Hunan Province Higher Education Key Laboratory of Modeling and Monitoring on the Near-Earth Electromagnetic Environments, Changsha University of Science & Technology, Changsha 410114 (China); Yi, Shihe; Cheng, Haifeng [College of Aerospace Science and Engineering, National University of Defense Technology, Changsha 410073 (China); Guo, Zhanhu; He, Qingliang [Chemical and Biomolecular Engineering Department, University of Tennessee, Knoxville, TN 37996 (United States)

2017-06-15

Highlights: • Theoretical formula and calculation results of effective permeability and effective permittivity of the Fe-C coaxial fiber are obtained based on the Maxwell equation. • The coaxial fiber has stronger anisotropy and better electromagnetic dissipation performance than the hollow carbon fiber and solid iron fiber with the same volume content. • Greater conductivity, larger aspect ratio, thin iron shell play important roles to improve the electromagnetic matching ability and microwave attenuation for the Fe-C coaxial fibers. - Abstract: Based on the Maxwell equation, the electromagnetic model in the coaxial fiber was described. The interaction with electromagnetic wave was analysed and the theoretical formula of axial permeability (μ{sub ∥}), axial permittivity (ε{sub ∥}), radial permeability (μ{sub ⊥}) and radial permittivity (ε{sub ⊥}) of Fe-C coaxial fiber were derived, and the demagnetization factor (N) of fibrous material was revised. Calculation results indicate that the composite fiber has stronger anisotropy and better EM dissipation performance than the hollow carbon fiber and solid iron fiber with the same volume content. These properties can be enhanced through increasing aspect ratio and carbon content. The μ{sub ‖} is 5.18-4.46i, μ{sub ⊥} is 2.58-0.50i, ε{sub ∥} is 7.63-6.97i, and ε{sub ⊥} is 1.98-0.15i when the electromagnetic wave frequency is 5 GHz with the outer diameter of 0.866 μm, inner diameter of 0.500 μm, and length of 20 μm. The maximum of the imaginary part of μ{sub ∥} and ε{sub ∥} are much larger than that of μ{sub ⊥} and ε{sub ⊥} when the structural parameters change, and the maximum of μ{sub ∥} and ε{sub ∥} can reach 6.429 and 23.59. Simulation results show that greater conductivity, larger aspect ratio, thin iron shell play important roles to improve the electromagnetic matching ability and microwave attenuation for the Fe-C coaxial fibers.

Valence and inner-valence shell dissociative photoionization of CO in the 26-33 eV range. II. Molecular-frame and recoil-frame photoelectron angular distributions

DEFF Research Database (Denmark)

Lebech, M.; Houver, J.C.; Raseev, G.

2012-01-01

Experimental and theoretical results for molecular-frame photoemission are presented for inner-valence shell photoionization of the CO molecule induced by linearly and circularly polarized light. The experimental recoil frame photoelectron angular distributions (RFPADs) obtained from dissociative...... photoionization measurements where the velocities of the ionic fragment and photoelectron were detected in coincidence, are compared to RFPADs computed using the multichannel Schwinger configuration interaction method. The formalism for including a finite lifetime of the predissociative ion state is presented...... for the case of general elliptically polarized light, to obtain the RFPAD rather than the molecular frame photoelectron angular distribution (MFPAD), which would be obtained with the assumption of instantaneous dissociation. We have considered photoionization of CO for the photon energies of 26.0 eV, 29.5 e...

K-Shell Photoabsorption Cross Sections for the Magnesium Isonuclear Sequence

Science.gov (United States)

Abdel-Naby, Shahin; Hasoglu, Fatih; Gorczyca, Thomas

2011-05-01

With the improved spectral resolution of launched X-ray telescopes, there is a demand for highly-accurate K-shell photoabsorption cross sections. Such data are needed for modeling astrophysical plasmas, interpreting the observed spectra from distant cosmic emitters, and determining the elemental abundances of the interstellar medium (ISM). Here we present new calculations for photoabsorption of the entire Mg isonuclear sequence using state-of-the-art R-matrix methods, including important spectator Auger broadening and inner-shell relaxation effects. Unlike our earlier work on carbon, oxygen, and neon ions, and the present work on multiply-ionized magnesium, the calculations for neutral Mg and singly-ionized Mg+ are complicated by additional M-shell occupancy, which leads to a larger R-matrix box and difficulties in implementing the quantum defect theoretical spectator Auger decay method for low-lying resonances. With the improved spectral resolution of launched X-ray telescopes, there is a demand for highly-accurate K-shell photoabsorption cross sections. Such data are needed for modeling astrophysical plasmas, interpreting the observed spectra from distant cosmic emitters, and determining the elemental abundances of the interstellar medium (ISM). Here we present new calculations for photoabsorption of the entire Mg isonuclear sequence using state-of-the-art R-matrix methods, including important spectator Auger broadening and inner-shell relaxation effects. Unlike our earlier work on carbon, oxygen, and neon ions, and the present work on multiply-ionized magnesium, the calculations for neutral Mg and singly-ionized Mg+ are complicated by additional M-shell occupancy, which leads to a larger R-matrix box and difficulties in implementing the quantum defect theoretical spectator Auger decay method for low-lying resonances. This work was funded in part by NASA's Astronomy Physics Research and Analysis (APRA) program.

Universal cross sections for K-shell ionization by low-velocity protons; importance of relativistic and energy-loss effects

International Nuclear Information System (INIS)

Zander, A.R.; Lapicki, G.

1981-01-01

When Z 1 2 , inner-shell ionization of a target atom of atomic number Z 2 by a projectile of atomic number Z 1 occurs predominately via removal of an inner-shell electron to the target atom continuum (direct ionization). Electron capture contributes then insignificantly to the ionization, and thus the predictions of perturbativein-Z 1 /Z 2 theories of direct ionization can be tested through comparison with measured ionization cross sections. We present such a comparison with the recently reported data for K-shell ionization of the Z 2 =22, 26, 28, and 30 elements by 60-150 keV protons (Z 1 =1). These ionization cross sections were inferred from x-ray production measurements using Krause's fluorescence yields

Discovery of Suprathermal Fe+ in and near Earth's Magnetosphere

Science.gov (United States)

Christon, S. P.; Hamilton, D. C.; Plane, J. M. C.; Mitchell, D. G.; Grebowsky, J. M.; Spjeldvik, W. N.; Nylund, S. R.

2017-12-01

Suprathermal (87-212 keV/e) singly charged iron, Fe+, has been observed in and near Earth's equatorial magnetosphere using long-term ( 21 years) Geotail/STICS ion composition data. Fe+ is rare compared to dominant suprathermal solar wind and ionospheric origin heavy ions. Earth's suprathermal Fe+ appears to be positively associated with both geomagnetic and solar activity. Three candidate lower-energy sources are examined for relevance: ionospheric outflow of Fe+ escaped from ion layers altitude, charge exchange of nominal solar wind Fe+≥7, and/or solar wind transported inner source pickup Fe+ (likely formed by solar wind Fe+≥7 interaction with near sun interplanetary dust particles, IDPs). Semi-permanent ionospheric Fe+ layers form near 100 km altitude from the tons of IDPs entering Earth's atmosphere daily. Fe+ scattered from these layers is observed up to 1000 km altitude, likely escaping in strong ionospheric outflows. Using 26% of STICS's magnetosphere-dominated data at low-to-moderate geomagnetic activity levels, we demonstrate that solar wind Fe charge exchange secondaries are not an obvious Fe+ source then. Earth flyby and cruise data from Cassini/CHEMS, a nearly identical instrument, show that inner source pickup Fe+ is likely not important at suprathermal energies. Therefore, lacking any other candidate sources, it appears that ionospheric Fe+ constitutes at least an important portion of Earth's suprathermal Fe+, comparable to observations at Saturn where ionospheric origin suprathermal Fe+ has also been observed.

Laboratory Calibration of X-ray Velocimeters for Radiation Driven Winds and Outflows Surrounding X-ray Binaries and Active Galactic Nuclei

Science.gov (United States)

Brown, Gregory V.; Beiersdorfer, P.; Graf, A.; Hell, N.; Liedahl, D.; Magee, E. W.; Träbert, E.; Beilmann, C.; Bernitt, S.; Crespo-Lopez-Urritiua, J.; Eberle, S.; Kubicek, K.; Mäckel, V.; Rudolph, J.; Steinbrügge, R.; Ullrich, J.; Kelley, R. L.; Kilbourne, C. A.; Leutenegger, M.; Porter, F. S.; Rasmussen, A.; Simon, M.; Epp, S.

2011-09-01

High resolution measurements of X-ray absorption and fluorescence by radiation driven winds and outflows surrounding X-ray binaries and AGN provide a powerful means for measuring wind velocities. The accuracy of these X-ray velocimeters is limited by the accuracy of atomic data. For example, in the case of the high mass X-ray binary Vela X-1 the uncertainty in the calculated transition wavelengths of the K alpha lines produced by photoionization and photoexcitation of Si L-shell ions is comparable to the likely Doppler shifts, making it impossible to determine a reliable velocity. Similar problems also exist in the case of absorption of X-rays by M-shell Fe ions, which produces in some AGN the so-called unresolved transition array across the 15-17 angstrom band. In this case, there is a 15-45 milliangstrom variation among different wavelength calculations. The uncertainty in the calculations makes it impossible to reliably determine the true velocity structure of the outflow, and in turn, prevents a reliable determination of the mass-loss rate of the AGN. We present results of a recent series of laboratory experiments conducted using an electron beam ion trap coupled with the LCLS X-ray free electron laser and the BESSY-II synchrotron and designed to calibrate the velocimeters provided by high resolution instruments on Chandra and XMM-Newton. We also present results of resonant photoexcitation measurements of the transition wavelength of an Fe XVI satellite line 'coincident' with the 2p-3d Fe XVII line 3D at 15.26 angstroms. This line has never been resolved using emission spectroscopy and its measurement confirms the intensity of line 3D is sensitive to the relative abundance of Fe XVI and XVII and thus temperature. Work at LLNL was performed under the auspices of DOE under contract DE-AC53-07NA27344 and supported by NASA's APRA program.

Study the Polyol Process of Preparing the ru Doped FePt Nanoparticles

Science.gov (United States)

Lee, Chih-Hao; Hsu, Jen-Ho; Su, Hui-Chia; Huang, Tzu Wen

The structure of Ru doped FePt nanoparticles using polyol process was studied. The particle size grown is around 5 nm, and a shell structure might be formed. By selecting the time and temperature of adding the Ru precursors into solution, three different processes to synthesize the FePtRu particles were studied resulting in different growing mechanics. The possible models during the reaction process are also discussed. The phase transition temperature for the as-grown FCC FePt nanoparticle to transform into L10 FePt nanoparticle is about 823 K which is about the same as the one without doping Ru atoms. From the XAS study of each element, the possible scenario is that: although Ru atoms with the size close to the Pt, they do not totally replace the Pt sites in the FePt alloy. Instead, most of Ru formed a shell outside the FePt nanoparticles and Fe atoms are replaced.

ECO-TECHNIQUE OF SEWER RENOVATION USING COMPOSITE SHELLS: STRUCTURAL ANALYSIS

Directory of Open Access Journals (Sweden)

B. Attaf

2015-07-01

Full Text Available An eco-technical renovation of the sewage system is developed in this paper; this technique involves incorporating into the existing sewer a series of jointed prefabricated sandwich or composite shells. The purpose of his study is to determine the structural shell deflection, the high displacement areas and to validate the non-failure criterion for each ply constituting the inner and outer laminate facings. The numerical results were obtained at low cost by using the finite element method. Studies have focused on structural analysis of a typical shell unit with an ovoid form (egg-shaped section when it is subjected, during annular space filling operation, to pressure forces generated by wet concrete. To ensure the safety of the composite shell structure, Tsai-Hill criterion function is applied and results are presented for the most stressed plies

Magnetic interaction reversal in watermelon nanostructured Cr-doped Fe nanoclusters

Energy Technology Data Exchange (ETDEWEB)

Kaur, Maninder; Dai, Qilin; Bowden, Mark; Engelhard, Mark; Wu, Yaqiao; Tang, Jinke; Qiang, You

2013-01-01

Cr-doped core-shell Fe/Fe-oxide nanoclusters (NCs) were synthesized at varied atomic percentages of Cr from 0 at. % to 8 at. %. The low concentrations of Cr (<10 at. %) were selected in order to inhibit the complete conversion of the Fe-oxide shell to Cr2O3 and the Fe core to FeCr alloy. The magnetic interaction in Fe/Fe-oxide NCs (rv25 nm) can be controlled by antiferromagnetic Cr-dopant. We report the origin of r-FeCr phase at very low Cr concentration (2 at. %) unlike in previous studies, and the interaction reversal from dipolar to exchange interaction in watermelon-like Cr-doped core-shell NCs. The giant magnetoresistance (GMR) effect,1,2 where an antiferromagnetic (AFM) exchange coupling exists between two ferromagnetic (FM) layers separated by a certain type of magnetic or non-magnetic spacer,3 has significant potential for application in the magnetic recording industry. Soon after the discovery of the GMR, the magnetic properties of multilayer systems (FeCr) became a subject of intensive study. The application of bulk iron-chromium (Fe-Cr) alloys has been of great interest, as these alloys exhibit favorable prop- erties including corrosion resistance, high strength, hardness, low oxidation rate, and strength retention at elevated temper- ature. However, the structural and magnetic properties of Cr-doped Fe nanoclusters (NCs) have not been investigated in-depth. Of all NCs, Fe-based clusters have unique magnetic properties as well as favorable catalytic characteristics in reactivity, selectivity, and durability.4 The incorporation of dopant of varied type and concentration in Fe can modify its chemical ordering, thereby optimizing its electrical, optical, and magnetic properties and opening up many new applications. The substitution of an Fe atom (1.24 A°) by a Cr atom (1.25 A° ) can easily modify the magnetic properties, since (i) the curie temperature (Tc ) of Fe is 1043 K, while Cr is an itinerant AFM with a bulk Neel temperature TN =311 K, and (ii) Fe

Tube-in-shell heat exchangers

International Nuclear Information System (INIS)

Richardson, J.

1976-01-01

Tube-in-shell heat exchangers normally comprise a bundle of parallel tubes within a shell container, with a fluid arranged to flow through the tubes in heat exchange with a second fluid flowing through the shell. The tubes are usually end supported by the tube plates that separate the two fluids, and in use the tube attachments to the tube plates and the tube plates can be subject to severe stress by thermal shock and frequent inspection and servicing are required. Where the heat exchangers are immersed in a coolant such as liquid Na such inspection is difficult. In the arrangement described a longitudinally extending central tube is provided incorporating axially spaced cylindrical tube plates to which the opposite ends of the tubes are attached. Within this tube there is a tubular baffle that slidably seals against the wall of the tube between the cylindrical tube plates to define two co-axial flow ducts. These ducts are interconnected at the closed end of the tube by the heat exchange tubes and the baffle comprises inner and outer spaced walls with the interspace containing Ar. The baffle is easily removable and can be withdrawn to enable insertion of equipment for inspecting the wall of the tube and tube attachments and to facilitate plugging of defective tubes. Cylindrical tube plates are believed to be superior for carrying pressure loads and resisting the effects of thermal shock. Some protection against thermal shock can be effected by arranging that the secondary heat exchange fluid is on the tube side, and by providing a thermal baffle to prevent direct impingement of hot primary fluid on to the cylindrical tube plates. The inner wall of the tubular baffle may have flexible expansible region. Some nuclear reactor constructions incorporating such an arrangement are described, including liquid metal reactors. (U.K.)

Assessing the prospects for achieving double-shell ignition on the National Ignition Facility using vacuum hohlraums

Science.gov (United States)

Amendt, Peter

2006-10-01

The goal of demonstrating ignition on the National Ignition Facility (NIF) has motivated a revisit of double-shell (DS) [1] targets as a complementary path to the baseline cryogenic single-shell approach [2]. Benefits of DS targets include room-temperature deuterium-tritium (DT) fuel preparation, minimal hohlraum-plasma-mediated laser backscatter, low threshold-ignition temperatures (4 keV) for relaxed hohlraum x-ray flux asymmetry tolerances [3], and loose shock timing requirements. On the other hand, DS ignition presents several challenges, including room-temperature containment of high-pressure DT (790 atm) in the inner shell; strict concentricity requirements on the two shells; development of nanoporous, low-density, metallic foams for structural support of the inner shell and hydrodynamic instability mitigation; and effective control of perturbation growth on the high-Atwood number interface between the DT fuel and the high-Z inner shell. Recent progress in DS ignition target designs using vacuum hohlraums is described, offering the potential for low levels of laser backscatter from stimulated Raman and Brillouin processes. In addition, vacuum hohlraums have the operational advantages of room temperature fielding and fabrication simplicity, as well as benefiting from extensive benchmarking on the Nova and Omega laser facilities. As an alternative to standard cylindrical hohlraums, a rugby-shaped geometry is also introduced that may provide energetics and symmetry tuning benefits for more robust DS designs with yields exceeding 10 MJ for 2 MJ of 3w laser energy. The recent progress in hohlraum designs and required advanced materials development are scheduled to culminate in a prototype demonstration of a NIF-scale ignition-ready DS in 2007. [1] P. Amendt et al., PoP 9, 2221 (2002). [2] J.D. Lindl et al., PoP 11, 339 (2004). [3] M.N. Chizhkov et al., Laser Part. Beams 23, 261 (2005). In collaboration with C. Cerjan, A. Hamza, J. Milovich and H. Robey.

La industria textil y su regulación en el siglo XVI: caso particular de Toledo = The textile industry and its regulation in the XVI century: Toledo, a particular case

Directory of Open Access Journals (Sweden)

María Ángela Jiménez Montañés

2012-01-01

Full Text Available ResumenEl sector al que correspondió el mayor protagonismo dentro de la industria europea moderna fue, sin lugar a dudas, el textil. Ello no representaba, en realidad, novedad alguna, pues la industria medieval se desarrolló precisamente en función primordialmente de la fabricación de tejidos. El vestido, al tiempo que una necesidad inmediata, resulta expresión visual de distinción social, aún más que la decoración de la vivienda. Por ello la industria textil creció a expensas tanto de la necesidad como del lujo. Uno de los grandes cambios que se producen en este tipo de industria durante todo el siglo XV y se consolida en el XVI se centra en las relaciones de producción, en la utilización de mano de obra campesina y la consolidación del ciclo de producción artesano rural. La mano de obra rural comienza a trabajar por su cuenta o en dependencia del empresario-productor de la ciudad. Si bien, la profunda transformación de la industria textil tendrá lugar en el siglo XVIII, con la revolución industrial.La transformación de la industria textil del siglo XVI propició la expansión de una nueva figura en el ámbito mercantil, que se denomina mercader-empresario, y por tanto, del sistema doméstico de producción conocido como Verlagssystem. Este nuevo sistema implicará modificaciones de factores claves para el desarrollo de las futuras sociedades mercantiles como pueden ser: el capital, la utilización de la materia prima y su proceso de transformación, la formación de los costes de producción y comercialización, la obtención de beneficios y su distribución, la concentración del capital y la generación de rentes. En definitiva, la creación de una nueva clase social, la burguesía. Este trabajo se centra en la industria sedera de la ciudad de Toledo en el siglo XVI.AbstractThe textile sector, was the greater protagonist, without doubt, within the modern European industry. It did not represent, in fact, newness some

Un caso d’amor fou nella società aristocratica genovese del secolo XVI

Directory of Open Access Journals (Sweden)

Gianfranco Bettin Lattes

2012-03-01

Full Text Available Perché nel cuore del centro storico di Genova esiste una “piazza dell’amor perfetto”? Sullo sfondo delle tumultuose vicende politiche del secolo XVI la passione, altrettanto tumultuosa, di Tommasina Spinola, nobile genovese, per Luigi XII, Re di Francia, trasforma l’amore in tragedia.

The projection of Inner Aspect in Vietnamese

Directory of Open Access Journals (Sweden)

Trang Phan

2013-06-01

Full Text Available Several semantic and syntactic distinctions, which have largely been neglected in the Vietnamese linguistic literature, are drawn together in this paper in a comparative context with other better-studied languages in order to indicate that Inner Aspect is projected within the VP shell and independently of the projection of Outer Aspect – a structural proposal originally advanced by Travis (2010. Overall, Vietnamese with its isolating character and rigid word order provides us with unusually direct evidence for an articulated VP structure.

CIRCUMSTELLAR SHELL FORMATION IN SYMBIOTIC RECURRENT NOVAE

Energy Technology Data Exchange (ETDEWEB)

Moore, Kevin; Bildsten, Lars [Department of Physics, Broida Hall, University of California, Santa Barbara, CA 93106 (United States)

2012-12-20

We present models of spherically symmetric recurrent nova shells interacting with circumstellar material (CSM) in a symbiotic system composed of a red giant (RG) expelling a wind and a white dwarf accreting from this material. Recurrent nova eruptions periodically eject material at high velocities ({approx}> 10{sup 3} km s{sup -1}) into the RG wind profile, creating a decelerating shock wave as CSM is swept up. High CSM densities cause the shocked wind and ejecta to have very short cooling times of days to weeks. Thus, the late-time evolution of the shell is determined by momentum conservation instead of energy conservation. We compute and show evolutionary tracks of shell deceleration, as well as post-shock structure. After sweeping up all the RG wind, the shell coasts at a velocity {approx}100 km s{sup -1}, depending on system parameters. These velocities are similar to those measured in blueshifted CSM from the symbiotic nova RS Oph, as well as a few Type Ia supernovae that show evidence of CSM, such as 2006X, 2007le, and PTF 11kx. Supernovae occurring in such systems may not show CSM interaction until the inner nova shell gets hit by the supernova ejecta, days to months after the explosion.

Hydrogen Production from Gasification of Palm Kernel Shell in the Presence of Fe/ CeO_2 Catalysts

International Nuclear Information System (INIS)

Anita Ramli; Mas Fatiha Mohamad; Suzana Yusup; Taufiq, Y.Y.H.

2016-01-01

Bio hydrogen is a renewable source of clean fuel and energy which can be derived from biomass. One of the suitable candidate as a source of biomass is palm kernel shell (PKS). Our initial work shows that bio hydrogen may be produced from PKS in the presence of zeolite supported catalysts. The potential of using cerium oxide (CeO_2) supported catalysts for the production of bio hydrogen from PKS is explored in this work using 2.5 - 10 % Fe loading. The catalysts were prepared by incipient wetness impregnation method and calcined at 500 degree Celsius for 16 h. The physicochemical properties of these catalysts were characterized using BET and XRD. The catalysts were tested in dry and steam gasification of PKS at 700 degree Celsius using PKS feeding rate of 2 g h"-"1 under N_2 atmosphere with biomass to catalyst ratio of 3:1 (wt/ wt). Steam to biomass ratio of 3.5:1 (wt/ wt) was used in steam gasification reaction. The gaseous products were analyzed using an on-line gas chromatography equipped with thermal conductivity detectors (TCD) and fitted with Molsieve 5A and Hayesep Q columns. Result shows that 2.5 % Fe/ CeO_2 gave the highest hydrogen production in both the dry and steam gasification of PKS. (author)

Crosstalk XVI, basic data communication and RS-232C

International Nuclear Information System (INIS)

Hwang, Hui Yung

1988-10-01

This book is divided into three parts, which deals with compatible software of data communication with IBM PC XT/AT. The first part consists of an introduction to crosstalk XVI, getting start for user, crosstalk practice, call with crosstalk, terminal feature, switch of communication parameter, terminal emulation, capturing data, transmission of text file answer mode, file transfer, command file and script file, command summary and examples. The second part deals with basic personal computer communication, RS-232C and explanation of communication control : RS-232C interface, transmission device and interrupt controller 8259.

Synthesis and characterization of fluorinated magnetic core-shell nanoparticles for inhibition of insulin amyloid fibril formation

International Nuclear Information System (INIS)

Skaat, Hadas; Margel, Shlomo; Belfort, Georges

2009-01-01

Maghemite (γ-Fe 2 O 3 ) magnetic nanoparticles of 15.0 ± 2.1 nm are formed by nucleation followed by controlled growth of maghemite thin films on gelatin-iron oxide nuclei. Uniform magnetic γ-Fe 2 O 3 /poly (2,2,3,3,4,4,4-heptafluorobutyl acrylate) (γ-Fe 2 O 3 /PHFBA) core-shell nanoparticles are prepared by emulsion polymerization of the fluorinated monomer 2,2,3,3,4,4,4-heptafluorobutyl acrylate (HFBA) in the presence of the maghemite nanoparticles. The kinetics of the insulin fibrillation process in the absence and in the presence of the γ-Fe 2 O 3 /PHFBA core-shell nanoparticles are elucidated. A significant direct slow transition from α-helix to β-sheets during insulin fibril formation is observed in the presence of the γ-Fe 2 O 3 /PHFBA nanoparticles. This is in contradiction to our previous manuscript, which illustrated that the γ-Fe 2 O 3 core nanoparticles do not affect the kinetics of the formation of the insulin fibrils, and to other previous publications that describe acceleration of the fibrillation process by using various types of nanoparticles. These core-shell nanoparticles may therefore be also useful for the inhibition of conformational changes of other amyloidogenic proteins that lead to neurodegenerative diseases such as Alzheimer's, Parkinson's, Huntington's, mad cow and prion diseases.

ORIGIN OF THE GALACTIC DIFFUSE X-RAY EMISSION: IRON K-SHELL LINE DIAGNOSTICS

Energy Technology Data Exchange (ETDEWEB)

Nobukawa, Masayoshi [Department of Teacher Training and School Education, Nara University of Education, Takabatake-cho, Nara, 630-8528 (Japan); Uchiyama, Hideki [Faculty of Education, Shizuoka University, 836 Ohya, Suruga-ku, Shizuoka, 422-8529 (Japan); Nobukawa, Kumiko K.; Koyama, Katsuji [Department of Physics, Graduate School of Science, Kyoto University, Kitashirakawa-oiwake-cho, Sakyo-ku, Kyoto, 606-8502 (Japan); Yamauchi, Shigeo, E-mail: nobukawa@nara-edu.ac.jp [Department of Physics, Nara Women’s University, Kitauoyanishimachi, Nara, 630-8506 (Japan)

2016-12-20

This paper reports detailed K-shell line profiles of iron (Fe) and nickel (Ni) of the Galactic Center X-ray Emission (GCXE), Galactic Bulge X-ray Emission (GBXE), Galactic Ridge X-ray Emission (GRXE), magnetic Cataclysmic Variables (mCVs), non-magnetic Cataclysmic Variables (non-mCVs), and coronally Active Binaries (ABs). For the study of the origin of the GCXE, GBXE, and GRXE, the spectral analysis is focused on equivalent widths of the Fe i-K α , Fe xxv-He α , and Fe xxvi-Ly α  lines. The global spectrum of the GBXE is reproduced by a combination of the mCVs, non-mCVs, and ABs spectra. On the other hand, the GRXE spectrum shows significant data excesses at the Fe i-K α and Fe xxv-He α  line energies. This means that additional components other than mCVs, non-mCVs, and ABs are required, which have symbiotic phenomena of cold gas and very high-temperature plasma. The GCXE spectrum shows larger excesses than those found in the GRXE spectrum at all the K-shell lines of iron and nickel. Among them the largest ones are the Fe i-K α , Fe xxv-He α , Fe xxvi-Ly α , and Fe xxvi-Ly β  lines. Together with the fact that the scale heights of the Fe i-K α , Fe xxv-He α , and Fe xxvi-Ly α lines are similar to that of the central molecular zone (CMZ), the excess components would be related to high-energy activity in the extreme envelopment of the CMZ.

A model for acoustic vaporization dynamics of a bubble/droplet system encapsulated within a hyperelastic shell.

Science.gov (United States)

Lacour, Thomas; Guédra, Matthieu; Valier-Brasier, Tony; Coulouvrat, François

2018-01-01

Nanodroplets have great, promising medical applications such as contrast imaging, embolotherapy, or targeted drug delivery. Their functions can be mechanically activated by means of focused ultrasound inducing a phase change of the inner liquid known as the acoustic droplet vaporization (ADV) process. In this context, a four-phases (vapor + liquid + shell + surrounding environment) model of ADV is proposed. Attention is especially devoted to the mechanical properties of the encapsulating shell, incorporating the well-known strain-softening behavior of Mooney-Rivlin material adapted to very large deformations of soft, nearly incompressible materials. Various responses to ultrasound excitation are illustrated, depending on linear and nonlinear mechanical shell properties and acoustical excitation parameters. Different classes of ADV outcomes are exhibited, and a relevant threshold ensuring complete vaporization of the inner liquid layer is defined. The dependence of this threshold with acoustical, geometrical, and mechanical parameters is also provided.

Shell finite element of reinforced concrete for internal pressure analysis of nuclear containment building

Energy Technology Data Exchange (ETDEWEB)

Lee, Hong Pyo, E-mail: hplee@kepri.re.k [Nuclear Power Laboratory, Korea Electric Power Research Institute, 103-16 Munji-Dong, Yuseong-Gu, Daejeon 305-380 (Korea, Republic of)

2011-02-15

Research highlights: Finite element program with 9-node degenerated shell element was developed. The developed program was mainly forced to analyze nuclear containment building. Concrete material model is adapted Niwa and Yamada failure criteria. The performance of program developed is verified through various numerical examples. The numerical analysis results similar to the experimental data. - Abstract: This paper describes a 9-node degenerated shell finite element (FE), an analysis program developed for ultimate pressure capacity evaluation and nonlinear analysis of a nuclear containment building. The shell FE developed adopts the Reissner-Mindlin (RM) assumptions to consider the degenerated shell solidification technique and the degree of transverse shear strain occurring in the structure. The material model of the concrete determines the level of the concrete stress and strain by using the equivalent stress-equivalent strain relationship. When a crack occurs in the concrete, the material behavior is expressed through the tension stiffening model that takes adhesive stress into account and through the shear transfer mechanism and compressive strength reduction model of the crack plane. In addition, the failure envelope proposed by Niwa is adopted as the crack occurrence criteria for the compression-tension region, and the failure envelope proposed by Yamada is used for the tension-tension region. The performance of the program developed is verified through various numerical examples. The analysis based on the application of the shell FE developed from the results of verified examples produced results similar to the experiment or other analysis results.

The Impact of Ceramic Shell Strength on Hot Tearing during Investment Casting

International Nuclear Information System (INIS)

Norouzi, Saeid; Farhangi, Hassan

2011-01-01

The effect of ceramic shell strength on hot tearing susceptibility during solidification was inspected practicing investment casting of the cobalt-base superalloy samples with the same casting conditions, but different ceramic shell systems. Results showed that the lower the ceramic shell strength upon using polymer additives, the lower the hindered contraction rate, and the lower the hindered contraction rate, the smaller the hot tearing tendency. Optical microscopy and electron microscopy scanning revealed that the hot tear propagated along the last solidified interdendritic phase, and that the hot tear surface had two major modes: 1) the ductile region in the outer layer; and 2) the inner region of liquid embrittlement.

Synthesis, characterization and biomedical application of multifunctional luminomagnetic core–shell nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Yi, Changqing [Key Laboratory of Biochip Technology, Biotech and Health Centre, Shenzhen Research Institutes of City University of Hong Kong, Shenzhen (China); Key Laboratory of Sensing Technology and Biomedical Instruments (Guangdong Province), School of Engineering, Sun Yat-Sen University, Guangzhou (China); Liu, Lei [Key Laboratory of Biochip Technology, Biotech and Health Centre, Shenzhen Research Institutes of City University of Hong Kong, Shenzhen (China); College of Chemistry and Environmental Science, Chemical Biology Key Laboratory of Hebei Province, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of Ministry of Education, Hebei University, Baoding (China); Li, Cheuk-Wing [Key Laboratory of Biochip Technology, Biotech and Health Centre, Shenzhen Research Institutes of City University of Hong Kong, Shenzhen (China); Zhang, Jinchao, E-mail: jczhang6970@163.com [Key Laboratory of Biochip Technology, Biotech and Health Centre, Shenzhen Research Institutes of City University of Hong Kong, Shenzhen (China); College of Chemistry and Environmental Science, Chemical Biology Key Laboratory of Hebei Province, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of Ministry of Education, Hebei University, Baoding (China); Yang, Mengsu, E-mail: bhmyang@cityu.edu.hk [Key Laboratory of Biochip Technology, Biotech and Health Centre, Shenzhen Research Institutes of City University of Hong Kong, Shenzhen (China)

2015-01-01

It has been well-established that nanomaterials provide a robust framework into which two or more functional moieties can be integrated to offer multifunctional and synergetic applications. We report here the facile synthesis and systematical investigation of the luminomagnetic core–shell nanoparticles (NPs) with the magnetic Fe{sub 3}O{sub 4} core coated with a silica shell incorporating fluorescent [Ru(bpy){sub 3}]{sup 2+}. The luminomagnetic NPs were monodisperse and spherical in shape with a diameter of 60 ± 10 nm. The luminomagnetic NPs possessed not only the desirable optical signature of Ru(bpy){sub 3}{sup 2+} but also the distinctive magnetic profile of Fe{sub 3}O{sub 4}, where a strong red-orange emission and the super-paramagnetic characteristics with the saturation magnetization values ca. 10 emu/g were observed for the luminomagnetic NPs. As revealed by Alamar blue assay and flow cytometry analysis, the Fe{sub 3}O{sub 4} NPs decrease the cell viability of HepG2 by ca. 10%, while an increase by ca. 10% on HepG2 cell proliferation was revealed after the silica shell was coated onto Fe{sub 3}O{sub 4} NPs, suggesting that the silica shell serves as a protective layer to increase the biocompatibility of the luminomagnetic NPs. Confocal laser scanning microscopy, transition electron microscopy and magnetic resonance (MR) images confirmed that the luminomagnetic NPs can enter into the interiors of HepG2 cells without damage, highlighting their capabilities for simultaneous optical fluorescence imaging and T2 MR imaging. Taking advantage of versatility of silica shell towards different surface modification protocols, the luminomagnetic NPs were successfully functionalized with epidermal growth factor receptor (EGFR) antibody for HepG2 cell recognition. All the results illustrated that the luminomagnetic NPs should be a potential candidate for future cancer diagnosis and therapy. - Highlights: • The luminomagnetic NPs were prepared by a water-in-oil reverse

Efficient one-pot sonochemical synthesis of thickness-controlled silica-coated superparamagnetic iron oxide (Fe3O4/SiO2) nanospheres

Science.gov (United States)

Abbas, Mohamed; Abdel-Hamed, M. O.; Chen, Jiangang

2017-12-01

A facile and eco-friendly efficient sonochemical approach was designed for the synthesis of highly crystalline Fe3O4 and Fe3O4/SiO2 core/shell nanospheres in single reaction. The generated physical properties (shock waves, microjets, and turbulent flows) from ultrasonication as a consequence of the collapse of microbubbles and polyvinylpyrrolidone (PVP) as a chemical linker were found to play a crucial role in the successful formation of the core/shell NPs within short time than the previously reported methods. Transmission electron microscopy revealed that a uniform SiO2 shell is successfully coated over Fe3O4 nanospheres, and the thickness of the silica shell could be easily controlled in the range from 5 to 15 nm by adjusting the reaction parameters. X-ray diffraction data were employed to confirm the formation of highly crystalline and pure phase of a cubic inverse spinel structure for magnetite (Fe3O4) nanospheres. The magnetic properties of the as-synthesized Fe3O4 and Fe3O4/SiO2 core/shell nanospheres were measured at room temperature using vibrating sample magnetometer, and the results demonstrated a high magnetic moment values with superparamagnetic properties.

PREFACE: Symmetries in Science XVI

Science.gov (United States)

2014-10-01

This volume of the proceedings ''Symmetries in Science XVI'' is dedicated to the memory of Miguel Lorente and Allan Solomon who both participated several times in these Symposia. We lost not only two great scientists and colleagues, but also two wonderful persons of high esteem whom we will always remember. Dieter Schuch, Michael Ramek There is a German saying ''all good things come in threes'' and ''Symmetries in Science XVI'', convened July 20-26, 2013 at the Mehrerau Monastery, was our third in the sequel of these symposia since taking it over from founder Bruno Gruber who instigated it in 1988 (then in Lochau). Not only the time seemed to have been perfect (one week of beautiful sunshine), but also the medley of participants could hardly have been better. This time, 34 scientists from 16 countries (more than half outside the European Union) came together to report and discuss their latest results in various fields of science, all related to symmetries. The now customary grouping of renowned experts and talented newcomers was very rewarding and stimulating for all. The informal, yet intense, discussions at ''Gasthof Lamm'' occurred (progressively later) each evening till well after midnight and finally till almost daybreak! However, prior to the opening ceremony and during the conference, respectively, we were informed that Miguel Lorente and Allan Solomon had recently passed away. Both attended the SIS Symposia several times and had many friends among present and former participants. Professor Peter Kramer, himself a long-standing participant and whose 80th birthday commemoration prevented him from attending SIS XVI, kindly agreed to write the obituary for Miguel Lorente. Professors Richard Kerner and Carol Penson (both also former attendees) penned, at very short notice, the tribute to Allan Solomon. The obituaries are included in these Proceedings and further tributes have been posted to our conference website. In 28 lectures and an evening poster

Optimization of the composition of bimetallic core/shell Fe2O3/Au nanoparticles for MRI/CT dual-mode imaging

International Nuclear Information System (INIS)

Zhang, Song; Qi, Yueyong; Yang, Hua; Gong, Mingfu; Zhang, Dong; Zou, Liguang

2013-01-01

Bimetallic core/shell Fe 2 O 3 /Au nanoparticles are promising candidate dual-mode contrast agents for magnetic resonance imaging (MRI) and computed tomography (CT) imaging. However, the gold coating on the hybrid nanoparticles (hybrids) affects the MRI and CT imaging quality. A thick gold nanoshell increases the X-ray attenuation effect but decreases the magnetic saturation of the hybrids. Therefore, we studied the effect of the Fe 2 O 3 and Au composition on these properties to find a suitable hybrid for MRI and CT imaging. Water-soluble, Au-coated magnetic nanoparticles were synthesized by iteratively reducing Au 3+ onto the Fe 2 O 3 surface via hydroxylamine seeding. The properties of the hybrids obtained after different numbers of Au seeding cycles were studied using transmission electron microscopy, UV–Vis spectrophotometry, a vibrating swatch gaussmeter, MRI, CT, and an MTT assay. The hybrids obtained after three Au seeding cycles had an Fe 2 O 3 :Au molar ratio of 7.2:26.8, a mean diameter of 48.3 nm, a UV–Vis absorbance peak of 550 nm, a saturation magnetization of 49.0 emu/g, and no cytotoxicity at a concentration of 500 μg/mL after incubation with RAW 264.7 cells for up to 72 h. The hybrids obtained after three Au seeding cycles are the preferred candidates for MRI and CT applications because of their relatively high R2 relaxivity (95 mM −1  s −1 ) and X-ray attenuation (1.87 times that of iodine) compared to those of the other hybrids investigated in this study

Magnetite Core-Shell Nanoparticles in Nondestructive Flaw Detection of Polymeric Materials.

Science.gov (United States)

Hetti, Mimi; Wei, Qiang; Pohl, Rainer; Casperson, Ralf; Bartusch, Matthias; Neu, Volker; Pospiech, Doris; Voit, Brigitte

2016-10-04

Nondestructive flaw detection in polymeric materials is important but difficult to achieve. In this research, the application of magnetite nanoparticles (MNPs) in nondestructive flaw detection is studied and realized, to the best of our knowledge, for the first time. Superparamagnetic and highly magnetic (up to 63 emu/g) magnetite core-shell nanoparticles are prepared by grafting bromo-end-group-functionalized poly(glycidyl methacrylate) (Br-PGMA) onto surface-modified Fe 3 O 4 NPs. These Fe 3 O 4 -PGMA NPs are blended into bisphenol A diglycidylether (BADGE)-based epoxy to form homogeneously distributed magnetic epoxy nanocomposites (MENCs) after curing. The core Fe 3 O 4 of the Fe 3 O 4 -PGMA NPs endows the MENCs with magnetic property, which is crucial for nondestructive flaw detection of the materials, while the shell PGMA promotes colloidal stability and prevents NP aggregation during curing. The eddy current testing (ET) technique is first applied to detect flaws in the MENCs. Through the brightness contrast of the ET image, surficial and subsurficial flaws in MENCs can be detected, even for MENCs with low content of Fe 3 O 4 -PGMA NPs (1 wt %). The incorporation of Fe 3 O 4 -PGMA NPs can be easily extended to other polymer and polymer-based composite systems and opens a new and very promising pathway toward MNP-based nondestructive flaw detection in polymeric materials.

Calculation of plastic deformation of a conical shell with the transformation of inner surface into outer one

Directory of Open Access Journals (Sweden)

A. I. Uvarov

2014-01-01

Full Text Available An analytical model of plastic deformation of a conical shell with the transformation of internal surface into outer one was developed with a use of the kinematic method. The shell material was assumed to be perfectly plastic. The theory of thin shells and the kinematic theorem of limit equilibrium were utilized in this work. Both geometric and physical nonlinearities were taken into account. Dependences for calculating radius of curvature of the intensive deformation zones, value of chain ring deformation and values of the deforming force as a function of axial displacement were determined. Analysis showed the possibility of using a conical shell to absorb energy with high efficiency. Obtained results could be used for calculation and selection of optimal parameters of the energy-absorbing elements in shock absorbers.

Design and analysis of reactor containment of steel-concrete composite laminated shell

International Nuclear Information System (INIS)

Ichikawa, K.; Isobata, O.; Kawamata, S.

1977-01-01

A new scheme of containment consisting of steel-concrete laminated shell is being developed. In the main part of a cylindrical vessel, the shell consists of two layers of thin steel plates located at the inner and outer surfaces, and a layer of concrete core into which both the steel plates are anchored. Because of the compressive and shearing resistance of the concrete core, the layers behave as a composite solid shell. Membrane forces are shared by steel plates and partly by concrete core. Bending moment is effectively resisted by the section with extreme layers of steel. Therefore, both surfaces can be designed as extremely thin plates: the inner plate, which is a load carrying members as well as a liner, can be welded without the laborious process of stress-relieving, and various jointing methods can be applied to the outer plate which is free from the need for leak tightness. The capability of the composite layers of behaving as a unified solid shell section depends largely on the shearing rigidity of the concrete core. However, as its resisting capacity to transverse shearing force is comparatively low, a device for reducing the shearing stress at the junction to the base mat is needed. In the new scheme, this part of the cylindrical shell is divided into multiple layers of the same kind of composite shell. This device makes the stiffness of the bottom of the cylindrical shell to lateral movement minimum while maintaining the proper resistance to membrane forces. The analysis shows that the transverse shearing stress can be reduced to less than 1√n of the ordinary case by dividing the thickness of the shell into n layers which are able to slip against each other at the contact surface. In order to validate the feasibility and safety of this new design, the results of analysis on the basis of up-to-date design loads are presented

Sinusoidal velaroidal shell – numerical modelling of the nonlinear ...

African Journals Online (AJOL)

The nonlinearity, applied to a sinusoidal velaroidal shell with the inner radius r0, the outer variables radii from 10m to 20m and the number of waves n=8, will give rise to the investigation of its nonlinear buckling resistance. The building material is a high-performant concrete. The investigation emphasizes more on the ...

Determination of K shell absorption jump factors and jump ratios of 3d transition metals by measuring K shell fluorescence parameters.

Science.gov (United States)

Kaçal, Mustafa Recep; Han, İbrahim; Akman, Ferdi

2015-01-01

Energy dispersive X-ray fluorescence technique (EDXRF) has been employed for measuring K-shell absorption jump factors and jump ratios for Ti, Cr, Fe, Co, Ni and Cu elements. The jump factors and jump ratios for these elements were determined by measuring K shell fluorescence parameters such as the Kα X-ray production cross-sections, K shell fluorescence yields, Kβ-to-Kα X-rays intensity ratios, total atomic absorption cross sections and mass attenuation coefficients. The measurements were performed using a Cd-109 radioactive point source and an Si(Li) detector in direct excitation and transmission experimental geometry. The measured values for jump factors and jump ratios were compared with theoretically calculated and the ones available in the literature. Copyright © 2014 Elsevier Ltd. All rights reserved.

Synthesis and characterization of FePt/Au core-shell nanoparticles

International Nuclear Information System (INIS)

Presa, P. de la; Multigner, M.; Morales, M.P.; Rueda, T.; Fernandez-Pinel, E.; Hernando, A.

2007-01-01

In this work, the structural and magnetic properties of the gold-coated FePt nanoparticles synthesized from high-temperature solution phase are presented. The amount of gold was optimized to obtain most of the FePt particles coated. The particle diameter increases from 4 to 10 nm as observed by TEM. The magnetic properties are largely affected by the coating. At low temperature, the coercive field Hc of the coated nanoparticles decreases about three times respect to the uncoated and the blocking temperature reduces to the half. The changes of the magnetic behavior are discussed in terms of the effect of the gold atoms at the FePt core surface

Vibrations of composite circular shell structures due to transient loads

International Nuclear Information System (INIS)

Schrader, K.-H.; Krutzik, N.; Winkel, G.

1975-01-01

Referring to a container consisting of different shell structures - such as spherical, cylindrical and conical shells - the dynamic behavior of coupled spatial shell structures due to transient loads will be investigated. The spatial structure including the filling of water will be idealized as a three-dimensional model consisting of ring elements. The influence of the water filling on the vibrations will be considered by virtual masses added to the shell structures. In circular direction as well as in meridional direction a consistent mass model has been used. By variation of the virtual masses it will be clarified, how these additional masses influence the vibrational behavior of the composed system. Another aspect which will be investigated is the influence of different stiffnesses of substructures or parts of substructures on the natural frequencies, and on their affiliated eigensystems. Furthermore, the maximum and minimum stresses in the structures caused by transient loads acting on the inner surface of the shells will be explored. Here it seems to be possible to locate an area of maximum strain. Rotational loads as well as nonrotational loads will be considered