Study in biosorption of lead, cadmium, nickel and zink to algae; Untersuchung der Biosorption von Blei, Cadmium, Nickel und Zink an Algen

Energy Technology Data Exchange (ETDEWEB)

Klimmek, S.; Stan, H.J. [Technische Univ. Berlin (Germany). Inst. fuer Lebensmittelchemie

1999-07-01

In a screening test, 25 algae have so far been examined for their ability to adsorb the four heavy metals Pb, Cd, Ni, Zn. The chlorophycea species Chlorella salina and the cynaophycea species Lyngbya taylorii proved the most efficient algae in the screening. The potential of algae as heavy metal adsorbers is shown by the example of Lyngbya taylorii. (orig.) [German] In einem Screeningverfahren wurden bisher 25 Algen auf ihre Faehigkeit, die vier Schwermetalle (Pb, Cd, Ni, Zn) zu adsorbieren, untersucht. Die Chlorophycee Chlorella salina und die Cyanophycee Lyngbya taylorii erwiesen sich als die leistungsfaehigsten Algen im Screening. Das Potential der Algen als Schwermetalladsorber wird am Beispiel von Lyngbya taylorii gezeigt. (orig.)

Thermoluminescence kinetic parameters of different amount La-doped ZnB2O4

International Nuclear Information System (INIS)

Kucuk, Nil; Gozel, Aziz Halit; Yüksel, Mehmet; Dogan, Tamer; Topaksu, Mustafa

2015-01-01

The kinetic parameters of 1%, 2%, 3% and 4% La-doped ZnB 2 O 4 phosphors (i.e. ZnB 2 O 4 :0.01La, ZnB 2 O 4 :0.02La, ZnB 2 O 4 :0.03La and ZnB 2 O 4 :0.04La) synthesized by nitric acid method have been calculated. Thermoluminescence (TL) glow curves of ZnB 2 O 4 :La phosphors after beta-irradiation showed a very well defined main peak having the maximum temperature at around 200 °C and a shoulder peak at around 315 °C with a constant heating rate of 5 °C/s. The kinetic parameters of ZnB 2 O 4 :La phosphors TL glow peaks (i.e. order of kinetics (b), activation energies (E a ) and frequency factors (s)) have been determined and evaluated by Computerized Glow Curve Deconvolution (CGCD), and Peak Shape (PS) methods using the glow curve data. From the results, it can conclude that the values of E a obtained with these methods for ZnB 2 O 4 :La phosphors are consistent with each other, but the s values differ considerably. - Highlights: • Calculation of TL kinetic parameters for La-doped ZnB 2 O 4 . • La-doped ZnB 2 O 4 was synthesized by nitric acid method. • Well defined main peak at about 200 °C

Magnetic anomaly in superconducting TmRh4B4

International Nuclear Information System (INIS)

Smith, J.L.; Huang, C.Y.; Tsou, J.J.; Ho, J.C.

1978-01-01

The magnetic and superconducting properties of TmRh 4 B 4 (which becomes superconducting at 9.6 K) by means of ac and dc magnetic susceptibility and specific heat measurements are investigated. At 10.7 K, an ac susceptibility peak similar to those found in spin glasses has been observed. In addition, a pronounced specific heat peak has been observed at 11.4 K. The susceptibility peak is essentially unaffected by substitution of 1% Lu or Er for the Tm, but it diminishes when much larger amounts of Er are substituted. The physical origin of this anomalous peak will be discussed

Stacking reactions of the borole complex Cp*Rh(η5-C4H4BPh) with the dicationic fragments [Cp*M]2+ (M = Rh or Ir)

International Nuclear Information System (INIS)

Loginov, D.A.; Muratov, D.V.; Starikova, Z.A.; Petrovskij, P.V.; Kudinov, A.R.

2006-01-01

The reaction of the (borole)rhodium iodide complex [(η-C 4 H 4 BPh)RhI] 4 with Cp*Li afforded the sandwich compound Cp*Rh(η-C 4 H 4 BPh) (1). The reactions of compound 1 with the solvated complexes [Cp*M(MeNO 2 ) 3 ] 2+ (BF 4 - ) 2 gave triple-decker cationic complexes with the central borole ligand [Cp*Rh(μ-η 5 :η 5 -C 4 H 4 BPh)MCp*] 2+ (BF 4 - ) 2 (M = Rh or Ir). The structure of complex 1 was established by X-ray diffraction [ru

A facile synthesis of ZnWO{sub 4} nanoparticles by microwave assisted technique and its application in photocatalysis

Energy Technology Data Exchange (ETDEWEB)

Garadkar, K.M., E-mail: kmg_chem@unishivaji.ac.in [Nanomaterials Research Laboratory, Department of Chemistry, Shivaji University, Kolhapur 416 004, MS (India); Ghule, L.A. [Nanomaterials Research Laboratory, Department of Chemistry, Shivaji University, Kolhapur 416 004, MS (India); Sapnar, K.B.; Dhole, S.D. [Microtron Accelerator Laboratory, Department of Physics, University of Pune, Pune 411 007, MS (India)

2013-03-15

Highlights: ► Nanocrystalline ZnWO{sub 4} particles were successfully prepared by a microwave method. ► Spherical morphology with a 10 nm size. ► The band is 3.4 eV. ► The photodegradation of RhB was 95% within 25 min. - Abstract: A simple microwave assisted technique has been successfully developed to synthesize ZnWO{sub 4} nanoparticles. The X-ray diffraction results indicated that the synthesized nanoparticles exhibited only wolframite structure. Structural, morphological and optical properties of ZnWO{sub 4} nanoparticles have been analyzed by XRD, SEM, TEM EDAX, UV–vis and FT-IR spectral measurements. The transmission electron microscopy (TEM) image revealed that particle size of ZnWO{sub 4} nanoparticles was found to be 10 nm, the band-gap of ZnWO{sub 4} nanoparticles was found to be 3.4 eV. The photocatalytic activities for aqueous Rhodamine B and Methylene Blue samples were investigated and observed that ZnWO{sub 4} nanoparticles exhibited highly enhanced photocatalytic activity towards RhB than MB.

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

Hyperfine fields at some 4d, 5d and 4f impurities in ferromagnetic GdZn and GdCd

International Nuclear Information System (INIS)

Kasamatsu, Y.; Kojima, K.; Hihara, T.

1995-01-01

Hyperfine (hf) fields at 4d (Y, Nb, Rh, Pd), 5d (Lu, Ta, Ir) and 4f (La, Nd, Sm, Eu) impurities in ferromagnetic GdZn and GdCd have been measured by NMR at 4.2 K. The local moment contributions to the hf field suggest that the impurity moments at the beginning and end of the d series are parallel and antiparallel to Gd moments, respectively. The hf results for 4f impurities are also discussed. ((orig.))

Measurement of 103mRh produced by the 103Rh(γ,γ')103mRh reaction with liquid scintillation counting

International Nuclear Information System (INIS)

Sekine, T.; Yoshihara, Kenji; Pavlicsek, I.; Lakosi, L.; Veres, A.

1989-01-01

A liquid scintillation counting technique was applied to measure the isotope 103m Rh (half life = 56.12 min) which is difficult to detect because its γ-ray is of low energy and low emission probability. Tris-(2,4-pentanedionato)rhodium(III) (Rh(acac) 3 ) was irradiated with bremsstrahlung of accelerated 3.2 MeV electrons by LINAC. The method has given a reliable calibration curve for the determination of 103m Rh radioactivity below Rh(acac) 3 concentrations of 2 mM. The integrated cross section of 103 Rh(γ,γ') 103m Rh determined by this method was found to be 6.8±3.4 μb MeV at 3.2 MeV. (author) 8 refs.; 5 figs

Development of a Tetrathioether (S4) Bifunctional Chelate System for Rh-105

Science.gov (United States)

2013-07-01

olt s...500 0 500 1000 1500 mV olt s -500 0 500 1000 1500 (B) Free Rhodium Chloride Minutes 0 2 4 6 8 10 12 mV olt s 0 2000 4000 mV olt s 0 2000 4000 (C) Rh-S4...Diol prepared in water Minutes 0 2 4 6 8 10 12 mV olts 0 2000 4000 mV olts 0 2000 4000 (D) 105 Rh-S4Diol with cold [Rh-S4(OH)2-Diol] +

Metal-organic-vapor-phase-epitaxy and characterization of homoepitaxial ZnO-layers; Metallorganische Gasphasenepitaxie und Charakteriesierung homoepitaktischer ZnO-Schichten

Energy Technology Data Exchange (ETDEWEB)

Heinze, Soeren

2009-03-30

layers was at the beginning very bad, but could by directed change of the growth parameters be more and more improved. By application of pure O{sub 2} as oxygen source (instead of N{sub 2}O) word-widely for the first time the homoepitactical deposition of ZnO layers in a two-dimensional growth mode succeeded. On the base of such layers attempts on the p-doping were performed with arsenic as dopant. Instead of p-type ZnO indeed an electrically insulating Zn/As/O alloy was formed. This alloy was identified as Zn{sub 3}(AlO{sub 3}){sub 2} -reinerite -. (orig.) [German] ZnO ist ein direkter Halbleiter mit einer Bandluecke von 3,37 eV und einer Exzitonenbindungsenergie von ca. 60 meV. Durch Legierung mit Cadmium oder Magnesium laesst sich die Bandluecke zwischen 2,9 eV und 4 eV variieren, was die Realisierung von z. B. Quantentopfstrukturen ermoeglicht. Deswegen ist ZnO ein aussichtsreiches Material fuer optoelektronische Anwendungen im blauen und nahen ultravioletten Spektralbereich. Trotz weltweit zahlreicher Forschungsaktivitaeten ueber die letzten Jahre konnte allerdings die Realisierung von p-Typ ZnO nicht zufriedenstellend (d. h. reproduzierbar und langzeitstabil) geloest werden. Die ZnO-Schichten dieser Arbeit wurden mittels metallorganischer Gasphasenepitaxie hergestellt. Anhand der Untersuchungen an heteroepitaktisch abgeschiedenen, undotierten Schichten, zeige ich die Grenzen der Heteroepitaxie auf. Durch die Einfuehrung eines dreistufigen Wachstumsverfahrens konnten physikalischen Eigenschaften (Morphologie, Lumineszenz, kristallografische und elektrische Eigenschaften) der obersten ZnO-Schicht deutlich verbessert werden. Dennoch konnte in Dotierversuchen kein p-Typ ZnO hergestellt werden. Hingegen wurde nachgewiesen, dass sich waehrend des Herstellungsprozesses eine elektrisch hochleitfaehige Zwischenschicht in der Naehe der Substrat/ZnO-Grenzflaeche bildet, deren Ausbildung sich bei der Heteroepitaxie nicht vermeiden laesst. Seit ca. drei Jahren sind Zn

Constructing Cd0.5Zn0.5S@ZIF-8 nanocomposites through self-assembly strategy to enhance Cr(VI) photocatalytic reduction.

Science.gov (United States)

Qiu, Jianhao; Zhang, Xiong-Fei; Zhang, Xingguang; Feng, Yi; Li, Yuxin; Yang, Lvye; Lu, Haiqiang; Yao, Jianfeng

2018-05-05

A novel and highly efficient photocatalyst of Cd 0.5 Zn 0.5 S@ZIF-8 nanocomposite has been developed by a facile self-assembly strategy. This is the first report on the application of Cd x Zn 1-x S and metal-organic framework (MOF) nanocomposite as photocatalysts for the reduction of Cr(VI). The resulting Cd 0.5 Zn 0.5 S@ZIF-8 exhibited higher photocatalytic activity than that of pristine Cd 0.5 Zn 0.5 S and ZIF-8. Particularly, the CZS@Z60 composite with 60 wt% of ZIF-8 exhibited a photocatalytic activity that is about 1.6 times as high as that of Cd 0.5 Zn 0.5 S. The dominant reason for the improved photocatalytic reduction potential is proved to be the newly-formed interfacial SZn bonds that firmly connect Cd 0.5 Zn 0.5 S and ZIF-8 and substantially improve the separation efficiency of photo-excited electrons and holes. The newly-formed chemical bonds are confirmed by XPS analyses, and the prolonged lifetime of photo-excited electrons is evidenced by the electrochemical measurement of photocurrent, which shows that the photocurrent on Cd 0.5 Zn 0.5 S@ZIF-8 is much higher than that of Cd 0.5 Zn 0.5 S and ZIF-8. This study clearly demonstrates that the MOF-based composite nanomaterials hold great promises for applications in the field of environmental remediation and for design of novel photocatalytic materials. Copyright © 2018 Elsevier B.V. All rights reserved.

Surfactant-free synthesis of octahedral ZnO/ZnFe2O4 heterostructure with ultrahigh and selective adsorption capacity of malachite green

Science.gov (United States)

Liu, Jue; Zeng, Min; Yu, Ronghai

2016-05-01

A new octahedral ZnO/ZnFe2O4 heterostructure has been fabricated through a facile surfactant-free solvothermal method followed by thermal treatment. It exhibits a record-high adsorption capacity (up to 4983.0 mg·g-1) of malachite green (MG), which is a potentially harmful dye in prevalence and should be removed from wastewater and other aqueous solutions before discharging into the environment. The octahedral ZnO/ZnFe2O4 heterostructure also demonstrates strong selective adsorption towards MG from two kinds of mixed solutions: MG/methyl orange (MO) and MG/rhodamine B (RhB) mixtures, indicating its promise in water treatment.

Modern completion and start-up techniques for petroleum wells on Mittelplate: Mittelplate A 3a and 8b; Moderne Komplettierung und Inproduktionssetzung von Erdoelbohrungen auf Mittelplate am Beispiel Mittelplate A 3a und 8b

Energy Technology Data Exchange (ETDEWEB)

Sauer, P. [RWE-DEA AG, Friedrichskoog (Germany). Foerderbetrieb Holstein

1998-12-31

The Mittelplate offshore platform is located 7 km offshore Schleswig-Holstein in the Wattenmeer national park. The contribution describes the completion and start-up operations. (orig.) [Deutsch] Seit ueber zehn Jahren betreibt das Mittelplate Konsortium die Bohr- und Foerderinsel Mittelplate. Sie liegt 7 km vor der Nordseekueste Schleswig-Holsteins im Nationalpark Wattenmeer an der Position von einer der drei vorausgegangenen Erkundungsbohrungen. Auf der mit Spundwaenden eingefassten kuenstlichen Insel befinden sich die notwendigen Foerder-, Aufbereitungs- und Zwischenlagereinrichtungen fuer Erdoel, als auch die Energieversorgungs-, Prozesssteuer- und Wohnbereiche. Ein in die Insel integrierter Hafen nimmt zum Abtransport des Reinoels eine der drei Oeltransport-Bargen auf, mit denen das Reinoel zum Anlanden nach Brunsbuettel gebracht wird. Am Beispiel der beiden in 1997 komplettierten Bohrungen Mittelplate A 3a und 8b soll im Folgenden ueber die Komplettierung und Inproduktionssetzung von Bohrungen auf Mittelplate berichtet werden. Es werden die Anforderungen an die Komplettierungstechnik vorgestellt und im Hinblick darauf die Beispielbohrungen erlaeutert. Abschliessend soll ein Blick in die Praxis der Komplettierungsarbeiten und der Inproduktionssetzung geworfen werden. (orig.)

Die Interhalogenkationen [Br2F5]+ und [Br3F8].

Science.gov (United States)

Ivlev, Sergei; Karttunen, Antti; Buchner, Magnus; Conrad, Matthias; Kraus, Florian

2018-05-02

Wir berichten über die Synthese und Charakterisierung der bislang einzigen Polyhalogenkationen, in denen verbrückende Fluoratome vorliegen. Das [Br2F5]+-Kation enthält eine symmetrische [F2Br-µ-F-BrF2]-Brücke, das [Br3F8]+-Kation enthält unsymmetrische µ-F-Brücken. Die Fluoronium-Ionen wurden in Form ihrer [SbF6]--Salze erhalten und Raman-, und 19F-NMR-spektroskopisch, sowie durch Röntgenbeugung am Einkristall untersucht. Quantenchemische Rechnungen, sowohl für die isolierten Kationen in der Gasphase, als auch für die Festkörper selbst, wurden durchgeführt. Populationsanalysen zeigen, dass die µ-F-Atome die am stärksten negativ partialgeladenen Atome der Kationen sind. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Preparation of Zn(BH4)2 and diborane and hydrogen release properties of Zn(BH4)2+xMgH2 (x=1, 5, 10, and 15)

Science.gov (United States)

Kwak, Young Jun; Kwon, Sung Nam; Song, Myoung Youp

2015-09-01

Zn(BH4)2 was prepared by milling ZnCl2 and NaBH4 in a planetary ball mill under Ar atmosphere, and Zn(BH4)2+xMgH2 (x=1, 5, 10, and 15) samples were prepared. Diborane (B2H6) and hydrogen release characteristics of the Zn(BH4)2 and Zn(BH4)2+xMgH2 samples were studied. The samples synthesized by milling ZnCl2 and NaBH4 contained Zn(BH4)2 and NaCl, together with small amounts of ZnCl2 and NaBH4. We designated these samples as Zn(BH4)2(+NaCl). The weight loss up to 400 °C of the Zn(BH4)2(+NaCl) sample synthesized by milling 4 h was 11.2 wt%. FT-IR analysis showed that Zn(BH4)2 was formed in the Zn(BH4)2(+NaCl) samples. MgH2 was also milled in a planetary ball mill, and mixed with the Zn(BH4)2(+NaCl) synthesized by milling for 4 h in a mortar and pestle. The weight loss up to 400 °C of Zn(BH4)2(+NaCl)+MgH2 was 8.2 wt%, corresponding to the weight % of diborane and hydrogen released from the Zn(BH4)2(+NaCl)+MgH2 sample, with respect to the sample weight. DTA results of Zn(BH4)2(+NaCl)+xMgH2 showed that the decomposition peak of Zn(BH4)2 was at about 61 °C, and that of MgH2 was at about 370-389 °C.

Contributions to multiple element speciation in vegetable plants: Studies on the type of bonding of numerous elements, particularly zinc and cadmium; Beitraege zur Multielement-Speziation in pflanzlichen Lebensmitteln: Studien zur Bindungsform zahlreicher Elemente unter besonderer Beruecksichtigung von Zink und Cadmium

Energy Technology Data Exchange (ETDEWEB)

Guenther, K.

1997-03-01

handelsueblichen - pflanzlichen Lebensmitteln nach Zellaufschluss bestimmt. Untersucht wurden Avocado, Bananen, Blumenkohl, Chicoree, Chinakohl, Dill, Eissalat (2 Proben), Endiviensalat, Feldsalat, Gurken, Kohlrabi, Kopfsalat, Mangold, Moehren, Paprika, Porree, Rettich, Rotkohl, Schnittsalat, Sellerie (2 Proben), Spinat, Topinambur, Weisskohl und Wurzelpetersilie. Der Zellaufschluss erfolgte durch eine Behandlung des Pflanzenmaterials mit einem elektrischen Dispergiergeraet (Ultra-Turrax) in Pufferloesung (liquid shearing). Durch nachfolgende Zentrifugation wurden die Homogenate in Ueberstaende (Cytosole) und Pellets aufgetrennt. Der Zellaufschluss der Pflanzen durch Verreiben mit Quarzsand nach Gefriertrocknung (solid shearing) ergab Blindwertprobleme bei einigen Elementen und war technisch umstaendlicher. In den untersuchten pflanzlichen Lebensmittel konnten im Durchschnitt mindestens 50% von Zn, Cd, Cu, Rb und K durch den Zellaufschluss durch Ultra-Turrax-Behandlung in Loesung ueberfuehrt werden. In vielen Faellen lag der cytosolbuertige Anteil dieser 5 Elemente bei>70%. Bei Zn und Cd war das Verhalten staerker pflanzenabhaengig als bei Zu, Rb und K. Alle 5 Elemente sind einer weiteren Speziation durch klassische Methoden damit zu einem grossen Anteil zugaenglich. Mn, Ca und besonders Fe und Sr waren durchschnittlich zum groessten Anteil an feste Zellbestandteile gebunden. Bei Ca und besonders Mn und Sr war das Loeslichkeitsverhalten jedoch sehr heterogen. Bei einigen Pflanzen betrug z.B. die Cytosolbuertigkeit von Mn und Sr ca. 90%, so dass in diesen Faellen eine umfassende Speziation ebenfalls moeglich ist. (orig./AJ)

Fe2O3/ZnO/ZnFe2O4 composites for the efficient photocatalytic degradation of organic dyes under visible light

Science.gov (United States)

Li, Xiaojuan; Jin, Bo; Huang, Jingwen; Zhang, Qingchun; Peng, Rufang; Chu, Shijin

2018-06-01

In this study, novel ternary Fe2O3/ZnO/ZnFe2O4 (ZFO) composites were successfully prepared through a simple hydrothermal reaction with subsequent thermal treatment. The as-prepared products were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Brunauer-Emmett-Teller (BET) analysis, Barrett-Joyner-Halenda (BJH) measurement, and UV-vis diffuse reflectance spectroscopy (UV-vis DRS). The photocatalytic degradation of rhodamine B (Rh B) under visible light irradiation indicated that the ZFO composites calcined at 500 °C has the best photocatalytic activity (the photocatalytic degradation efficiency can reach up to 95.7% within 60 min) and can maintain a stable photocatalytic degradation efficiency for at least three cycles. In addition, the photocatalytic activity of ZFO composites toward dye decomposition follows the order cationic Rh B > anionic methyl orange. Finally, using different scavengers, superoxide and hydroxyl radicals were identified as the primary active species during the degradation reaction of Rh B.

Probing the electronic properties of ternary AnM3n−1B2n (n = 1: A = Ca, Sr; M = Rh, Ir and n = 3: A = Ca, Sr; M = Rh phases: observation of superconductivity

Directory of Open Access Journals (Sweden)

Hiroyuki Takeya, Mohammed ElMassalami, Luis A Terrazos, Raul E Rapp, Rodrigo B Capaz, Hiroki Fujii, Yoshihiko Takano, Mathias Doerr and Sergey A Granovsky

2013-01-01

Full Text Available We follow the evolution of the electronic properties of the titled homologous series when n as well as the atomic type of A and M are varied where for n = 1, A = Ca, Sr and M = Rh, Ir while for n = 3, A = Ca, Sr and M = Rh. The crystal structure of n = 1 members is known to be CaRh2B2-type (Fddd, while that of n = 3 is Ca3Rh8B6-type (Fmmm; the latter can be visualized as a stacking of structural fragments from AM3B2 (P6/mmm and AM2B2. The metallic properties of the n = 1 and 3 members are distinctly different: on the one hand, the n = 1 members are characterized by a linear coefficient of the electronic specific heat γ ≈ 3 mJ mol−1 K−2, a Debye temperature θD ≈ 300 K, a normal conductivity down to 2 K and a relatively strong linear magnetoresistivity for fields up to 150 kOe. The n = 3 family, on the other hand, exhibits γ ≈ 18 mJ mol−1 K−2, θD ≈ 330 K, a weak linear magnetoresistivity and an onset of superconductivity (for Ca3Rh8B6, Tc = 4.0 K and Hc2 = 14.5 kOe, while for Sr3Rh8 B6, Tc = 3.4 K and Hc2 ≈ 4.0 kOe. These remarkable differences are consistent with the findings of the electronic band structures and density of state (DOS calculations. In particular, satisfactory agreement between the measured and calculated γ was obtained. Furthermore, the Fermi level, EF, of Ca3Rh8B6 lies at almost the top of a pronounced local DOS peak, while that of CaRh2B2 lies at a local valley: this is the main reason behind the differences between the, e.g., superconducting properties. Finally, although all atoms contribute to the DOS at EF, the contribution of the Rh atoms is the strongest.

Probing the electronic properties of ternary AnM3n−1B2n (n = 1: A = Ca, Sr; M = Rh, Ir and n = 3: A = Ca, Sr; M = Rh) phases: observation of superconductivity

Science.gov (United States)

Takeya, Hiroyuki; ElMassalami, Mohammed; Terrazos, Luis A; Rapp, Raul E; Capaz, Rodrigo B; Fujii, Hiroki; Takano, Yoshihiko; Doerr, Mathias; Granovsky, Sergey A

2013-01-01

We follow the evolution of the electronic properties of the titled homologous series when n as well as the atomic type of A and M are varied where for n = 1, A = Ca, Sr and M = Rh, Ir while for n = 3, A = Ca, Sr and M = Rh. The crystal structure of n = 1 members is known to be CaRh2B2-type (Fddd), while that of n = 3 is Ca3Rh8B6-type (Fmmm); the latter can be visualized as a stacking of structural fragments from AM3B2 (P6/mmm) and AM2B2. The metallic properties of the n = 1 and 3 members are distinctly different: on the one hand, the n = 1 members are characterized by a linear coefficient of the electronic specific heat γ ≈ 3 mJ mol−1 K−2, a Debye temperature θD ≈ 300 K, a normal conductivity down to 2 K and a relatively strong linear magnetoresistivity for fields up to 150 kOe. The n = 3 family, on the other hand, exhibits γ ≈ 18 mJ mol−1 K−2, θD ≈ 330 K, a weak linear magnetoresistivity and an onset of superconductivity (for Ca3Rh8B6, Tc = 4.0 K and Hc2 = 14.5 kOe, while for Sr3Rh8 B6, Tc = 3.4 K and Hc2 ≈ 4.0 kOe). These remarkable differences are consistent with the findings of the electronic band structures and density of state (DOS) calculations. In particular, satisfactory agreement between the measured and calculated γ was obtained. Furthermore, the Fermi level, EF, of Ca3Rh8B6 lies at almost the top of a pronounced local DOS peak, while that of CaRh2B2 lies at a local valley: this is the main reason behind the differences between the, e.g., superconducting properties. Finally, although all atoms contribute to the DOS at EF, the contribution of the Rh atoms is the strongest. PMID:27877576

Zinc terephthalates ZnC_8H_4O_4 as anodes for lithium ion batteries

International Nuclear Information System (INIS)

Wang, Liping; Zou, Jian; Chen, Shulin; Yang, Jingyi; Qing, Fangzhu; Gao, Peng; Li, Jingze

2017-01-01

Graphical abstract: Both of well-crystalline and amorphous zinc terephthalates ZnC_8H_4O_4 are synthesized and amorphous structure demonstrates a higher capacity and better cycling performance. - Highlights: • Crystalline and amorphous ZnC_8H_4O_4 are obtained. • Both crystalline and amorphous ZnC_8H_4O_4 have σ_e of 10"−"7 S m"−"1. • Lithium ion diffusion is the rate-determine process. • Amorphous has a high capacity and durable performance. • Amorphous ZnC_8H_4O_4 has a high apparent lithium ion diffusion coefficient. - Abstract: Organic materials offer the advantages of cost-effective, environmental benignity, and molecular structural diversity as applications of electrode materials for lithium ion batteries. In fact, their lithium storage behaviors in terms of dynamics and kinetics intrinsically lie in ion migration in solids. Thus the solid forms including crystalline and amorphous states are crucial for the properties. In this study, a conventional carbonyl type organic material, namely zinc terephthalate (ZnC_8H_4O_4), is obtained in both well-crystalline and amorphous forms and applied as anodes for lithium ion batteries. ZnC_8H_4O_4 with amorphous structure shows higher lithium storage capacity and better capacity retention compared with that of crystalline one. It is ascribed that the amorphous phase provides a higher lithium ion diffusion coefficient than the crystalline one under the conditions of similar electronic conductivity.

SrNi{sub 7.90(8)}In{sub 5.10(8)}. A new superstructure in the NaZn{sub 13} family

Energy Technology Data Exchange (ETDEWEB)

Hoffmann, Rolf-Dieter; Poettgen, Rainer [Inst. fuer Anorganische und Analytische Chemie and NRW Graduate School of Chemistry, Univ. Muenster (Germany); Muts, Ihor [Inst. fuer Anorganische und Analytische Chemie and NRW Graduate School of Chemistry, Univ. Muenster (Germany); Inorganic Chemistry Dept., Ivan Franko National Univ., Lviv (Ukraine); Zaremba, Vasyl [Inorganic Chemistry Dept., Ivan Franko National Univ., Lviv (Ukraine)

2009-07-01

SrNi{sub 7.90(8)}In{sub 5.10(8)} was synthesized by induction melting of the elements in a sealed tantalum tube in a water-cooled silica sample chamber. The structure was refined on the basis of single crystal X-ray diffractometer data: Cccm, a = 1615.2(4), b = 1822.3(4), c = 1238.5(4) pm, wR2 = 0.1481, 4144F{sup 2} values and 150 variables. The striking structural motifs of the SrNi{sub 7.90}In{sub 5.10} structure are one-dimensional [Ni{sub 7} ] cluster units (242-286 pm Ni-Ni) which are surrounded by indium atoms. The structural relationship to the other NaZn{sub 13} superstructures is discussed on the basis of a group-subgroup scheme. (orig.)

Probing the electronic properties of ternary A n M3n-1B2n (n = 1: A = Ca, Sr; M = Rh, Ir and n = 3: A = Ca, Sr; M = Rh) phases: observation of superconductivity.

Science.gov (United States)

Takeya, Hiroyuki; ElMassalami, Mohammed; Terrazos, Luis A; Rapp, Raul E; Capaz, Rodrigo B; Fujii, Hiroki; Takano, Yoshihiko; Doerr, Mathias; Granovsky, Sergey A

2013-06-01

We follow the evolution of the electronic properties of the titled homologous series when n as well as the atomic type of A and M are varied where for n = 1, A = Ca, Sr and M = Rh, Ir while for n = 3, A = Ca, Sr and M = Rh. The crystal structure of n = 1 members is known to be CaRh 2 B 2 -type ( Fddd ), while that of n = 3 is Ca 3 Rh 8 B 6 -type ( Fmmm ); the latter can be visualized as a stacking of structural fragments from AM 3 B 2 ( P 6/ mmm ) and AM 2 B 2 . The metallic properties of the n = 1 and 3 members are distinctly different: on the one hand, the n = 1 members are characterized by a linear coefficient of the electronic specific heat γ ≈ 3 mJ mol -1 K -2 , a Debye temperature θ D ≈ 300 K, a normal conductivity down to 2 K and a relatively strong linear magnetoresistivity for fields up to 150 kOe. The n = 3 family, on the other hand, exhibits γ ≈ 18 mJ mol -1 K -2 , θ D ≈ 330 K, a weak linear magnetoresistivity and an onset of superconductivity (for Ca 3 Rh 8 B 6 , T c = 4.0 K and H c2 = 14.5 kOe, while for Sr 3 Rh 8 B 6 , T c = 3.4 K and H c2 ≈ 4.0 kOe). These remarkable differences are consistent with the findings of the electronic band structures and density of state (DOS) calculations. In particular, satisfactory agreement between the measured and calculated γ was obtained. Furthermore, the Fermi level, E F , of Ca 3 Rh 8 B 6 lies at almost the top of a pronounced local DOS peak, while that of CaRh 2 B 2 lies at a local valley: this is the main reason behind the differences between the, e.g., superconducting properties. Finally, although all atoms contribute to the DOS at E F , the contribution of the Rh atoms is the strongest.

Design and Investigation of Optical Properties of N-(Rhodamine-B)-Lactam-Ethylenediamine (RhB-EDA) Fluorescent Probe.

Science.gov (United States)

Soršak, Eva; Volmajer Valh, Julija; Korent Urek, Špela; Lobnik, Aleksandra

2018-04-14

This study presents chemical modification of a Rhodamine B (RhB) sensor probe by ethylenediamine (EDA), and investigation of its spectral as well as sensor properties to the various metals. The synthesised N -(Rhodamine-B)-lactam-ethylenediamine (RhB-EDA) fluorescent probe shows interesting optical sensor properties, and high sensitivity and selectivity to Ag⁺ ions among all the tested metal ions (K⁺, Mg 2+ , Cu 2+ , Ni 2+ , Fe 2+ , Pb 2+ , Na⁺, Mn 2+ , Li⁺, Al 3+ , Co 2+ , Hg 2+ , Sr 2+ , Ca 2+ , Ag⁺, Cd 2+ and Zn 2+ ), while the well-known Rhodamine B (RhB) fluorescent probe shows much less sensitivity to Ag⁺ ions, but high sensitivity to Fe 2+ ions. The novel fluorescent sensor probe RhB-EDA has the capabilities to sense Ag⁺ ions up to µM ranges by using the fluorescence quenching approach. The probe displayed a dynamic response to Ag⁺ in the range of 0.43 × 10 -3 -10 -6 M with a detection limit of 0.1 μM. The sensing system of an RhB-EDA novel fluorescent probe was optimised according to the spectral properties, effect of pH and buffer, photostability, incubation time, sensitivity, and selectivity. Since all the spectral and sensing properties were tested in green aqueous media, although many other similar sensor systems rely on organic solvent solutions, the RhB-EDA sensing probe may be a good candidate for measuring Ag⁺ ions in real-life applications.

Sequential heavy metal extraction from dust precipitates and road sediments. Part 2. Sequential heavy metal extraction from urban dust; Sequentielle Schwermetallextraktion aus Staubniederschlaegen und Strassensedimenten. T. 2. Sequentielle Schwermetallextraktion von staedtischen Staeuben

Energy Technology Data Exchange (ETDEWEB)

Heiser, U.; Norra, S.; Stueben, D.; Wagner, M. von [Karlsruhe Univ. (T.H.) (Germany). Inst. fuer Petrographie und Geochemie

1999-03-01

For the application of our method for the sequential extraction of heavy metals from microsamples presented in part 1 (`Sequentielle Schwermetallextraktion von Mikroproben` - `Sequential Extraction of Heavy Metals from Micro Samples`) an investigation was carried out to evaluate airborne dust fallout and street sediments at two urban sites where different heavy metal immission rates occur due to traffic influence. In the street sediments the total concentrations of zinc, copper and lead was three to fivefold higher in the silt and clay fraction (<63 {mu}m) than in the particle size fraction (<1,12 mm), but showed nearly the same mobilisation behaviour. The dust samples showed equal mobilisation behaviour as the street sediments for copper and lead, while zinc was considerably more mobile in the dust samples: In extraction steps I-IV (I: mobile fraction; II: easily deliverable fraction; III: fraction bound to manganese oxides; IV: fraction bound organic to matter) zinc, copper and lead in street sediments, as well as copper and lead in dust samples, were dissolved to 40-70%, whereas about 80% of zinc in the dust samples was already dissolved in extraction step I. (orig.) [Deutsch] Mit Hilfe des in Teil 1 (`Sequentielle Schwermetallextraktion von Mikroproben`) vorgestellten Verfahrens zur sequentiellen Schwermetallextraktion von Mikroproben wurden die Mobilisierbarkeiten von Zink, Kupfer und Blei aus Staubniederschlaegen und aus der Schluff- und Tonfraktion von Strassensedimenten an zwei urbanen Standorten mit unterschiedlicher, verkehrsbedingter Schwermetallbelastung untersucht und miteinander verglichen. In Strassensedimenten wiesen Zink, Kupfer und Blei in der Schluff- und Tonfraktion drei- bis fuenffach hoehere Gesamtgehalte auf als die Korngroessenfraktion <1,12 mm, zeigten aber aehnliches Verhalten in der Mobilisierbarkeit. Bei den Staubproben war die Mobilisierbarkeit von Kupfer und Blei aehnlich wie in den Strassensedimenten, waehrend sich Zink als erheblich

Band gap-engineered ZnO and Ag/ZnO by ball-milling method and their photocatalytic and Fenton-like photocatalytic activities

International Nuclear Information System (INIS)

Choi, Young In; Jung, Hye Jin; Shin, Weon Gyu; Sohn, Youngku

2015-01-01

Graphical abstract: - Highlights: • Ag/ZnO hybrid materials were prepared by a ball-milling method. • Adsorption and photocatalytic dye degradation were tested for pure RhB under visible light. • Adsorption and photocatalytic dye degradation were tested for mixed dye (MO + RhB + MB) under visible light. • Fenton-like photocatalytic activity (H 2 O 2 addition effects) was examined. - Abstract: The hybridization of ZnO with Ag has been performed extensively to increase the efficiency of ZnO in various applications, including catalysis. In this study, a wet (w) and dry (d) ball-milling method was used to hybridize Ag with ZnO nanoparticles, and their physicochemical properties were examined. Visible light absorption was enhanced and the band gap was engineered by ball-milling and Ag hybridization. Their photocatalytic activities were tested with rhodamine B (RhB) and a mixed dye (methyl orange + RhB + methylene blue) under visible light irradiation. For pure RhB, the photocatalytic activity was decreased by ball-milling and was observed in the order of ZnO(d) < Ag/ZnO(d) < ZnO(w) < Ag/ZnO(w) ≤ ZnO(ref). For the degradation of RhB and methylene blue (MB) in the mixed dye (or the simulated real contaminated water), the photocatalytic activity was observed in the order of Ag/ZnO(d) < ZnO(d) < ZnO(w) < Ag/ZnO(w) ≤ ZnO(ref). When the photodegradation tested with H 2 O 2 addition, however, the Fenton-like photocatalytic activity was reversed and the ZnO(ref) showed the poorest activity for the degradation of RhB and methylene blue (MB). In the mixed dye over all the catalysts, methyl orange (MO) was degraded most rapidly. The relative degradation rates of RhB and MB were found to be dependent on the catalyst and reaction conditions.

Superconducting properties of Zn and Al double-doped Mg1-x(Zn0.5Al0.5)xB2

DEFF Research Database (Denmark)

Xu, G.J.; Grivel, Jean-Claude; Abrahamsen, A.B.

2004-01-01

(XRD), ac susceptibility, magnetization and resistivity. The double doping leads to decreases in both the lattice parameters a and c, and the T-c decreases with increasing dopant content. A systematical comparison with Al doped- and Li, Al double doped MgB2 of structure, superconducting transition......A series of polycrystalline samples of Mg1-x(Zn0.5Al0.5)(x)B-2 (0less than or equal toxless than or equal to0.8) were prepared by solid state reaction method and their structure, superconducting transition temperature (T-c) and transport properties were investigated by means of X-ray diffraction...

Biosorption phenomena of chromium, copper, iron and zink by dispersed bacterial extracellular polymeric substance

International Nuclear Information System (INIS)

Zainus Salimin; Endang Nuraeni; Mirawaty

2015-01-01

Heavy metals removing is generally performed using chemical coagulant that generates the chemical pollutant, so it is necessary to replace it by another alternative material as the Extracellular Polymeric Substance (EPS) resulting from the extraction of bacteria. The EPS contains the negatively functional groups (RCOOH, ROPO 3 H, ROPO 3 Na, ROSO 3 H, ROSO 3 Na, etc) as the cation sorbent and the positively functional groups (ROH, RC(NH 2 )HCOOH, etc) as the anion sorbent. The EPS absorbs the ion pollutants, then EPS containing the loaded metals be settled by gravitation. The utilization of EPS for removing of chromium, copper, iron, and zink was performed for biosorption phenomena study. Two hundred mg of EPS is mixed with 300 ml of the liquid waste having the pH of 2,4 containing 3,06 ppm of chromium; 4,83 ppm of copper; 1,6 ppm of iron and 15,07 ppm of zink. The solution is then agitated on 150 rpm and the pH of 7. The separated water supernatant is then sampled every 2 hours for its analysis of metals content. The experiment is repeated again for the solution pH of 4 and 8. The results of experiment indicates that the EPS composition are 11% of polysaccharides, 77% of protein, and 11% of fat ,and EPS contains the chemical bounding of C-H, OH, NH, and C=O. Indicating that EPS contains RCOOH, ROH and (RC(NH 2 )HCOOH. The best condition for metals biosorption is pH 8, and on the 6 hours of process time, the metal concentration on the water supernatant for chromium, copper, iron and zinc are 0,99 ppm; 0,51 ppm; 0,17 ppm; and 4,61 ppm respectively. Its selectivities are Fe 3+ > Cr 3+ >Cu 2+ >Fe 2+ >Zn 2+ , on the 6 hours of process time the location of cations functional groups was filled by the cations of Cr 3+ ,Cu 2+ , dan Fe 2+ . The cation of Zn 2+ enters to that location on the end of period so on the 6 hours of process time its concentration of 4,61 ppm not conforms to its concentration of regulation value of 2 ppm. On the process time of 6 hours the removing

IT-Compliance nach COBIT: Gegenüberstellung zwischen COBIT 4.0 und COBIT 5

OpenAIRE

Klotz, Michael

2014-01-01

Mit der aktuellen fünften Version (COBIT 5) wurden grundlegende Erweiterungen und Änderungen des COBIT-Frameworks vorgenommen. Inwieweit sich dies auf das IT-Compliance-Verständnis und das Management von IT-Compliance ausgewirkt hat, wird in diesem Arbeitspapier untersucht. Hierzu werden die vierte und die fünfte Version von COBIT auf ihre compliance-relevanten Aussagen hin untersucht und vergleichend gegenübergestellt. Im Ergebnis weist COBIT 4.0 in seiner Struktur zahlreiche Inkonsistenzen ...

Band gap-engineered ZnO and Ag/ZnO by ball-milling method and their photocatalytic and Fenton-like photocatalytic activities

Energy Technology Data Exchange (ETDEWEB)

Choi, Young In [School of Chemistry and Biochemistry, Yeungnam University, Gyeongsan, Gyeongbuk 38541 (Korea, Republic of); Jung, Hye Jin [Department of Mechanical Engineering, Chungnam National University, Daejeon 34134 (Korea, Republic of); Shin, Weon Gyu, E-mail: wgshin@cnu.ac.kr [Department of Mechanical Engineering, Chungnam National University, Daejeon 34134 (Korea, Republic of); Sohn, Youngku, E-mail: youngkusohn@ynu.ac.kr [School of Chemistry and Biochemistry, Yeungnam University, Gyeongsan, Gyeongbuk 38541 (Korea, Republic of)

2015-11-30

Graphical abstract: - Highlights: • Ag/ZnO hybrid materials were prepared by a ball-milling method. • Adsorption and photocatalytic dye degradation were tested for pure RhB under visible light. • Adsorption and photocatalytic dye degradation were tested for mixed dye (MO + RhB + MB) under visible light. • Fenton-like photocatalytic activity (H{sub 2}O{sub 2} addition effects) was examined. - Abstract: The hybridization of ZnO with Ag has been performed extensively to increase the efficiency of ZnO in various applications, including catalysis. In this study, a wet (w) and dry (d) ball-milling method was used to hybridize Ag with ZnO nanoparticles, and their physicochemical properties were examined. Visible light absorption was enhanced and the band gap was engineered by ball-milling and Ag hybridization. Their photocatalytic activities were tested with rhodamine B (RhB) and a mixed dye (methyl orange + RhB + methylene blue) under visible light irradiation. For pure RhB, the photocatalytic activity was decreased by ball-milling and was observed in the order of ZnO(d) < Ag/ZnO(d) < ZnO(w) < Ag/ZnO(w) ≤ ZnO(ref). For the degradation of RhB and methylene blue (MB) in the mixed dye (or the simulated real contaminated water), the photocatalytic activity was observed in the order of Ag/ZnO(d) < ZnO(d) < ZnO(w) < Ag/ZnO(w) ≤ ZnO(ref). When the photodegradation tested with H{sub 2}O{sub 2} addition, however, the Fenton-like photocatalytic activity was reversed and the ZnO(ref) showed the poorest activity for the degradation of RhB and methylene blue (MB). In the mixed dye over all the catalysts, methyl orange (MO) was degraded most rapidly. The relative degradation rates of RhB and MB were found to be dependent on the catalyst and reaction conditions.

Self-assembled ZnGa2O4–RGO nanocomposites and their enhanced adsorption and photocatalytic performance in water treatment

International Nuclear Information System (INIS)

Huang, K.; Zhao, X.S.; Li, Y.F.; Xu, X.; Liang, C.; Fan, D.Y.; Yang, H.J.; Zhang, R.; Wang, Y.G.; Lei, M.

2014-01-01

Highlights: • ZnGa 2 O 4 –RGO nanocomposites by a self-assembly approach under facile solvothermal condition. • ZnGa 2 O 4 NPs have a well-controlled size and uniform distribution. • The water treatment process is formed by two successive parts: adsorption and photocatalytic degradation. • The content of RGO sheets is crucial for optimizing the photocatalytic activity with a key value of 5%. - Abstract: ZnGa 2 O 4 nanoparticles (NPs) have been successfully anchored onto reduced graphene oxide (RGO) nanosheets by a self-assembly approach under facile solvothermal condition. The as-synthesized ZnGa 2 O 4 –RGO nanocomposites were investigated by X-ray diffraction (XRD), field emission scanning electron microscope (FESEM) and transmission electron microscope (TEM). The results reveal that ZnGa 2 O 4 NPs with a well-controlled size and uniform distribution were successfully assembled onto RGO sheets. Moreover, both methylene blue (MB) and rhodamine B (RhB) were employed as model pollutants to evaluate the ability of as-prepared ZnGa 2 O 4 –RGO nanocomposites for wastewater treatment. The content of RGO sheets was found to be crucial for optimizing the photocatalytic activity of various nanocomposites with a key value of 5% beyond which the adsorption ability of ZnGa 2 O 4 –RGO nanocomposites for dyes dominates the process of water treatment

Koper en zink voor landbouwhuisdieren

NARCIS (Netherlands)

Makking, C.; Jongbloed, A.W.

2004-01-01

De EU heeft de maximaal toegestande hoeveelheden koper en zink in voeders voor landbouwhuisdieren verlaagd. Uit onderzoek van ASG blijkt dat de nieuwe normen geen negatieve consequenties hoeven te hebben voor de dierlijke productie

Electrochemical dissolution characteristics of Zn, Mg, Al and ZnMg(Al) alloys

OpenAIRE

Rossrucker, Lisa (M. Sc.)

2016-01-01

Thema der Dissertation ist die Untersuchung des elektrochemischen Auflösungsverhaltens von Zink, Magnesium, Aluminium und von zinkreichen Gusslegierungen. Um detallierte Einblicke in den Mechanismus der Korrosion dieser Materialien zu erhalten, wurde eine mikroelektrochemische Durchflusszelle mit verschiedenen Online-Analysemethoden gekoppelt. Hierfür wurde zur Quantifizierung der Metallauflösung ein UV-VIS-Spektrometer bzw. ein induktiv gekoppeltes Plasma-Massenspektrometer verwendet. Zur An...

Bromine-rich Zinc Bromides: Zn6Br12(18-crown-6)2×(Br2)5, Zn4Br8(18-crown-6)2×(Br2)3, and Zn6Br12(18-crown-6)2×(Br2)2.

Science.gov (United States)

Hausmann, David; Feldmann, Claus

2016-06-20

The bromine-rich zinc bromides Zn6Br12(18-crown-6)2×(Br2)5 (1), Zn4Br8(18-crown-6)2×(Br2)3 (2), and Zn6Br12(18-crown-6)2×(Br2)2 (3) are prepared by reaction of ZnBr2, 18-crown-6, and elemental bromine in the ionic liquid [MeBu3N][N(Tf)2] (N(Tf)2 = bis(trifluoromethylsulfonyl)amide). Zn6Br12(18-crown-6)2×(Br2)5 (1) is formed instantaneously by the reaction. Even at room temperature, compound 1 releases bromine, which was confirmed by thermogravimetry (TG) and mass spectrometry (MS). The release of Br2 can also be directly followed by the color and density of the title compounds. With controlled conditions (2 weeks, 25 °C, absence of excess Br2) Zn6Br12(18-crown-6)2×(Br2)5 (1) slowly releases bromine with conconcurrent generation of Zn4Br8(18-crown-6)2×(Br2)3 (2) (in ionic liquid) and Zn6Br12(18-crown-6)2×(Br2)2 (3) (in inert oil). All bromine-rich zinc bromides contain voluminous uncharged (e.g., Zn3Br6(18-crown-6), Zn2Br4(18-crown-6)) or ionic (e.g., [Zn2Br3(18-crown-6)](+), [(Zn2Br6)×(Br2)2](2-)) building units with dibromine molecules between the Zn oligomers and partially interconnecting the Zn-containing building units. Due to the structural similarity, the bromine release is possible via crystal-to-crystal transformation with retention of the crystal shape.

Monoclinic superstructure of Pr{sub 3}Rh{sub 4}Ge{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Vosswinkel, Daniel; Hoffmann, Rolf-Dieter; Greiwe, Magnus; Eul, Matthias; Poettgen, Rainer [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie

2016-07-01

Pr{sub 3}Rh{sub 4}Ge{sub 4} was synthesized by melting of the elements in an arc-melting furnace followed by annealing in a sealed tantalum ampoule in a muffle furnace. Structure refinement was based on temperature dependent single-crystal X-ray diffractometer data. At ambient temperature Pr{sub 3}Rh{sub 4}Ge{sub 4} adopts the U{sub 3}Ni{sub 4}Si{sub 4} type structure with strongly enhanced anisotropic displacement parameters for Rh1. Below 230 K additional reflections start to appear and at 110 K the structure could be described with the (3+1)D superspace group I2/m(α0γ)00; α=1/2, γ=1/2; (Z=2). This commensurately modulated structure could be refined with 1448 F{sup 2} values, 39 variables and residuals of wR=0.0417 for the main reflections and wR=0.1520 for the satellites of 1{sup st} order, [a=408.36(2), b=421.12(3) and c=2504.4(2) pm]. The commensurate description could be transformed to a 3D supercell with space group A2/m and Z=4: a=816.72(2), b=421.12(3), c=2537.5(1) pm, β=99.26(1) , 1448 F{sup 2} values, 69 variables and wR=0.0499. The relation of the U{sub 3}Ni{sub 4}Si{sub 4} type structure, the (3+1)D modulated and the 3D supercell is discussed on the basis of a group-subgroup scheme. Temperature dependent magnetic susceptibility data reveal Curie-Weiss paramagnetism with an experimental moment of 3.72(2) μ{sub B}/Pr atom and a Weiss constant of -12.6(5) K. No magnetic ordering is evident down to 3 K.

Enhanced photocatalytic activity of nanocellulose supported zinc oxide composite for RhB dye as well as ciprofloxacin drug under sunlight/visible light

Science.gov (United States)

Tavker, Neha; Sharma, Manu

2018-05-01

Zinc oxide nanoparticles were synthesised from zinc acetate di-hydrate via co-precipitation method. Nanocellulose was isolated from agrowaste using chemo-mechanical treatments and characterized. Nanocellulose supported zinc oxide composites were prepared through in-situ method by adding different amounts of nanocellulose. The photocatalytic efficiency of pure Zno and nanocellulose supported ZnO was calculated using RhB dye under visible light and sun light. The composites which had nanocellulose in greater ratio showed higher degradation efficiency in sunlight rather than visible light for both; dye and drug. All the composites showed high rate of photodegradation compared to bare ZnO and bare nanocellulose. The enhancement in photocatalytic activity was observed maximum where the amount of cellulose was maximum. The maximum observed rate was 0.025 min-1 using Ciprofloxacin drug due to the increase in lifetime of Z4 sample delaying the electron and hole pair recombination. The degrading efficiency of nanocellulose supported zinc oxide (NC/ZnO) composite for RhB was found to be 35% in visible, 76% in sunlight and 75% for ciprofloxacin under sunlight.

Industrie 4.0-Strategien und Reifegrad

OpenAIRE

Hofmann, Erik; Oettmeier, Katrin

2017-01-01

Industrie 4.0 ist in aller Munde. Ermöglicht wird diese «vierte industrielle Revolution» durch die flexible digitale Vernetzung von Objekten (z.B. Produkten oder Maschinen) über das Internet und andere Netzwerkdienste. Im Rahmen der Fokusstudie «SCM 4.0: Supply Chain Management und digitale Vernetzung» wird der aktuelle Stand der Implementierung von Industrie 4.0 bei Schweizer Unternehmen analysiert. Anhand einer grosszahligen Erhebung wird dabei neben dem derzeitigen Reifegrad auch die vo...

1,8-Diazabicyclo[5.4.0]undec-7-en-8-ium bromido(phthalocyaninatozincate

Directory of Open Access Journals (Sweden)

Bartosz Przybył

2014-06-01

Full Text Available The title compound, (C9H17N2[ZnBr(C32H16N8], contains a bromido(phthalocyaninatozincate anion and a protonated 1,8-diazabicyclo[5.4.0]undece-7-ene cation, [DBUH]+. The central ZnII atom has a distorted square-pyramidal geometry, with four isoindole N atoms of the macrocycle in equatorial positions and a bromide ion in the axial position. The latter has a relatively high displacement parameter, but no evidence for disorder was obtained. The central ZnII atom is displaced by 0.488 (3 Å from the mean plane defined by the four isoindole N atoms. The [DBUH]+ cation is involved in an almost linear N—H...Br hydrogen bond. In the crystal, π–π interactions lead to a relatively short distance of 3.366 (3 Å between the phthalocyaninate rings.

Magnetic ordering and electrical resistivity in Co0.2Zn0.8Fe2O4 spinel oxide

International Nuclear Information System (INIS)

Bhowmik, R.N.; Ranganathan, R.; Ghosh, B.; Kumar, S.; Chattopadhyay, S.

2008-01-01

We report the magnetic, Moessbauer spectroscopy and resistivity measurements in order to understand the electronic behaviour of bulk Co 0.2 Zn 0.8 Fe 2 O 4 spinel oxide. The effect of magnetic order on electrical behaviour is observed from the resistivity measurements in the absence and presence of magnetic field. The analysis of Moessbauer spectra suggests the absence of Fe 2+ ions in the system, which implies that complete hopping of charge carriers between localized Fe 3+ /Co 2+ and Fe 2+ /Co 3+ pair of ions in B sublattice is not the favourable mechanism in Co 0.2 Zn 0.8 Fe 2 O 4 . We suggest that electrical behaviour of the present sample may be consistent with a model of fractional charge transfer via Fe B 3+ -O 2- -Co B 2+ superexchange path

Thermoelectric ZnO and ZnAl2O4

DEFF Research Database (Denmark)

Sommer, Sanna

2015-01-01

ZnO har vist sig at være et lovende termoelektrisk materiale. Den høje termiske ledningsevne kræver at man forsker i at finde en måde at sænke den. Tilstedeværelsen af både ZnAl2O4 og ZnO har vist sig at sænke den termiske ledningsevne for ZnO. Berardan et al. [5] har vist at når ZnAl2O4...... is tilstede på baggrund af en for høj aluminium doping koncentration under syntese af ZnO, så medfører tilstedeværelsen af ZnAl2O4 at zT sænkes. Modsat, så har Jood et al. vist at tildstedeværelsen af ZnAl2O4 kan medføre en aftagende termisk ledningsevne. På trods af en samtidig sænkning af den elektriske...... ledningsevne giver det overordnet en øget zT. Baillieul [29] har [20] syntetiseret ZnAl2O4 og ZnO separat, hvorefter krystalliterne er presset sammen. Det viser sig at medføre en øget elektrisk ledningsevne kombineret med aftagende termiske ledningsevne. Disse resultater viser at tilstedeværelsen af ZnAl2O4...

Effect of superconductivity on spin dynamics in (Y/sub 1-x/Re/sub x/)Rh4B4

International Nuclear Information System (INIS)

Kumagai, K.; Fradin, F.Y.

1982-01-01

An adiabatic field-cycle method has been used to study spin dynamics of RE ions in (Y/sub 1-x/RE/sub x/)Rh 4 B 4 . Longitudinal dipolar fluctuations of RE moments are found to be the main source of the nuclear spin-lattice relaxation time of 11 B. The variation of T 1 in the superconducting state is attributed to the reduction of the electronic spin-relaxation time, tau/sub m/, which is mainly determined by the RKKY type interaction mediated by the conduction electrons. 3 figures

Jern og zink i cerealier

DEFF Research Database (Denmark)

Persson, Daniel Olof; Hansen, Thomas Hesselhøj; Thomsen, Rikke Pape

2009-01-01

Mangel på mikronæringsstoffer, især jern og zink, er et udbredt og voksende problem for mennesker i mange udviklingslande. Det skyldes, at cerealer som ris og hvede udgør den dominerende fødekilde. Konsekvensen er en række negative indvirkninger på menneskers sundhed, udvikling, arbejdsevne og...

SYNTHESIS AND STRUCTURAL CHARACTERIZATION OF A Zn(II COORDINATION POLYMER BASED ON 4,4’-BIPYRIDINE AND ACETATO

Directory of Open Access Journals (Sweden)

LI-HUA WANG

2015-05-01

Full Text Available A novel Zn(II coordination polymer, [Zn(bpy(acetato2]n (bpy = 4,4’-bipyridine, has been synthesized and characterized by elemental analysis and single-crystal X-ray diffraction. The Zn(II coordination polymer is triclinic, space group P-1 with a = 8.046(3 Å, b = 9.161(3 Å, c = 10.663(3 Å, α = 109.769(4º, β = 99.966(5º, γ = 101.666(5º, V= 699.1(4 Å3, Z = 2, Dc = 1.614 mg·m-3, μ = 1.774 mm-1, F(000 = 348, and final R1 = 0.0541, ωR2 = 0.1605. X-ray diffraction analysis reveals that the Zn(II center is six-coordination with a N2O4 distorted octahedral coordination environment. The Zn(II complex forms 1D chain structure by the bridge of 4,4’-bipyridine and acetato.

Random laser based on Rhodamine 6G (Rh6G doped poly(methyl methacrylate (PMMA films coating on ZnO nanorods synthesized by hydrothermal oxidation

Directory of Open Access Journals (Sweden)

Hua Zhang

Full Text Available Random laser based on Rh6G doped PMMA thin films coating on ZnO nanorods synthesized by a simple hydrothermal oxidation method has been demonstrated. This kind of random laser medium is based on waveguide structure consisting of ZnO nanorods, Rh6G doped PMMA film and air. By controlling the time of hydrothermal oxidation reaction, wheat-like and hexagonal prism ZnO nanorods have been successfully fabricated. The emission spectra of these gain mediums based on different ZnO nanorods are different. The one based on wheat-like ZnO nanorods mainly exhibits amplified spontaneous emission, and the other one based on hexagonal prism ZnO nanorods shows random laser emission. The threshold of the random laser medium is about 73.8 μJ/pulse, and the full width at half maximum (FWHM is around 2.1 nm. The emission spectra measured at different detecting angles reveal that the output direction is strongly confined in ±30° by the waveguide effect. Our experiments demonstrate a promising method to achieve organic random laser medium. Keywords: Random laser, ZnO nanorods, Hydrothermal oxidation, Rhodamine 6G (Rh6G, Poly(methyl methacrylate (PMMA

A Novel Orange-Red Emitting ZnB4O7:Eu3+ Phosphor with Urchin-Like Nanostructure

Directory of Open Access Journals (Sweden)

Hom Nath Luitel

2015-01-01

Full Text Available A novel phosphor, ZnB4O7:Eu3+, with urchin-like structure consisting of radially arranged high density nanorods was successfully synthesized by hydrothermal process at 150°C for 24 h. The nanorods were measured from 200 to 400 nm in diameter and several µm in length. The urchins were few µm to 40 µm in diameter. The ZnB4O7:Eu3+ phosphors were efficiently excited by ultraviolet (UV ~ 254 nm to visible light of ~ 220 to 450 nm and exhibited intense orange-red emission consisting of main peaks at 590, 615, and 695 nm due to the charge transfer in the host and f→f transitions (5D0 to 7F1,2,4 of the Eu3+ ions. Effect of the Eu3+ ions concentration on the photoluminescence (PL emission intensity was investigated and it was found that 5 at% Eu3+ is the optimum concentration. Meanwhile, the concentration quenching mechanism was discussed. The key parameters, such as temperature dependent PL and CIE values of ZnB4O7:Eu3+ phosphors, were studied. The ZnB4O7:Eu3+ phosphor exhibited good thermal stability and better absorption cross section compared to the commercial Y2O2S:Eu3+ phosphor. All these characteristics indicate that the phosphor will be a potential candidate for the UV based white LEDs.

La5Zn2Sn

Directory of Open Access Journals (Sweden)

Igor Oshchapovsky

2011-11-01

Full Text Available A single crystal of pentalanthanum dizinc stannide, La5Zn2Sn, was obtained from the elements in a resistance furnace. It belongs to the Mo5SiB2 structure type, which is a ternary ordered variant of the Cr5B3 structure type. The space is filled by bicapped tetragonal antiprisms from lanthanum atoms around tin atoms sharing their vertices. Zinc atoms fill voids between these bicapped tetragonal antiprisms. All four atoms in the asymmetric unit reside on special positions with the following site symmetries: La1 (..m; La2 (4/m..; Zn (m.2m; Sn (422.

Development and characterization of La/B{sub 4}C multilayer systems as X-ray mirrors in the energy range 100-200 eV; Entwicklung und Charakterisierung von La/B{sub 4}C-Multischichtsystemen als Roentgenspiegel im Energiebereich 100-200 eV

Energy Technology Data Exchange (ETDEWEB)

Hendel, Stefan

2009-01-15

The main topics of this thesis are the development and characterization of La/B{sub 4}C multilayer systems. For this these materials were evaluated and characterized for the applied electron-beam evaporation. For the monitoring of the evaporation process two separate in-situ layer thicknesses were available. For periodic multilayer systems the X-ray reflectometry used for Mo/Si multilayers was accepted. Because of the change from Mo/Si on La/B{sub 4}C the driving of the evaporation process had to be material-conditionedly further developed and optimized. For the fabrication of aperiodic La/B{sub 4}C multilayer systems additionally an in-situ ellipsometer was taken into operation. Furthermore a decreasement of the interface roughnesses and by this following increasement of the reflectivities of La/B{sub 4}C multilayers by polishing of the single layers with accelerated ions during the fabrication shall be studied. The fabricated multilayers are characterized and evaluated concerning roughnesses, reflectivities, ans spectral band width. [German] Im Mittelpunkt dieser Arbeit stehen die Entwicklung und Charakterisierung von La/B{sub 4}C-Multischichtsystemen. Dazu wurden diese Materialien fuer die verwendete Elektronenstrahlverdampfung evaluiert und charakterisiert. Fuer die Ueberwachung des Aufdampfprozesses standen zwei separate In-situ Schichtdickenkontrollen zur Verfuegung. Fuer periodische Multischichtsysteme wurde die fuer Mo/Si-Multischichten genutzte Roentgenreflektometrie uebernommen. Aufgrund des Wechsels von Mo/Si auf La/B{sub 4}C musste materialbedingt die Steuerung des Verdampfungsprozesses weiterentwickelt und optimiert werden. Fuer die Herstellung aperiodischer La/B{sub 4}C-Multischichtsysteme wurde zusaetzlich ein In-situ Ellipsometer in Betrieb genommen. Des Weiteren soll eine Senkung der Grenzflaechenrauigkeiten und damit einhergehende Erhoehung der Reflektivitaeten von La/B{sub 4}C-Multischichten durch das Polieren mit beschleunigten Ionen der

Effect of supplementation of Zn-biocomplex in ration on the growth of young sheep

Directory of Open Access Journals (Sweden)

Supriyati

2007-12-01

Full Text Available The effect of supplementation of graded levels of Zn-bio-complex in concentrate on the growth of young sheep was studied. Fourty young Thin Tailled sheeps were devided into 4 groups of Zn-bio complex treatments. Zink-bio-complex was produced by IRIAP’s laboratory. King grass powder (CP = 10.4% and concentrate (CP=15.5% were given as a basal diet. King grass powder and drinking water were given ad libitum. The concentrate was given daily at 200 g h-1d-1 supplemented with 0 mg Zn kg-1 of DM (R1, 50 mg Zn kg-1 of DM (R2, 100 mg Zn kg-1 of DM (R3, and 200 mg Zn kg-1 of DM (R4. The initial live weight of sheep was 11.99 ± 0.17kg h-1. Live weight were measured fortnightly and feed consumption were measured daily. The experiment was carried out for 12 weeks with 4 weeks prior adaptation periods. Data obtained were analyzed statistically based on Completely Randomized Design. The results of experiment showed that the supplementation of Zn-bio-complex improved the live weight from 57.60 g h-1d-1 (R1 to 85.47, 72.14 and 67.86 g h-1d-1 with the feed conversion ratio improvement from 11.9 (R1 to 8.0, 9.6 and 10.5 for treatment R2, R3 and R4 respectively (P0.05 for R1, R2, R3 and R4, respectively. It can be concluded that the supplementation of Zn-bio-complex at the level of 50 mg Zn kg-1 in daily concentrate resulted in the best response on live weight gain and feed conversion ratio of young sheep.

Ternary scandium-rich indides Sc{sub 50}T{sub 13}In{sub 3} and Sc{sub 50}Rh{sub 13}In{sub 3}O{sub y} (T = Rh, Ir; y {approx} 8) - synthesis and crystal structure

Energy Technology Data Exchange (ETDEWEB)

Zaremba, R.; Poettgen, R. [Inst. fuer Anorganische und Analytische Chemie, Univ. Muenster (Germany)

2007-12-15

New intermetallic compounds Sc{sub 50}Rh{sub 13.3}In{sub 2.7} and Sc{sub 50}Ir{sub 13.6}In{sub 2.4} and the suboxides Sc{sub 49.2}Rh{sub 13}In{sub 3.8}O{sub 8.8} and Sc{sub 49.2}Rh{sub 13.7}In{sub 2.8}O{sub 8.0} were synthesized from the elements or with Sc{sub 2}O{sub 3} as an oxygen source, respectively, in sealed tantalum tubes in a water-cooled sample chamber of an induction furnace. They crystallize with a new cubic structure type, space group F m anti 3, a = 1772.5(6) pm, wR2 = 0.032, 1111 F{sup 2} values, 34 variables for Sc{sub 50}Rh{sub 13.3}In{sub 2.7}, a = 1766.5(6) pm, wR2 = 0.041, 745 F{sup 2} values, 34 variables for Sc{sub 50}Ir{sub 13.6}In{sub 2.4}, a = 1764.4(2) pm, wR2 = 0.044, 640 F{sup 2} values, 41 variables for Sc{sub 49.2}Rh{sub 13}In{sub 3.8}O{sub 8.8}, and a = 1761.5(6) pm, wR2 = 0.054, 740 F{sup 2} values, 42 variables for Sc{sub 49.2}Rh{sub 13.7}In{sub 2.8}O{sub 8.0}. The main structural motifs are rhodium-centered indium cubes in an fcc like arrangement in which the octahedral and tetrahedral voids are filled by In2Sc{sub 12} and In1Sc{sub 12} icosahedra, respectively, resembling a Li{sub 3}Bi-like structure. The Rh1 (Ir1) and Sc4 atoms lie between these polyhedral units. The oxygen atoms partially fill Sc{sub 6} octahedra in Sc{sub 49.2}Rh{sub 13}In{sub 3.8}O{sub 8.8} and Sc{sub 49.2}Rh{sub 13.7}In{sub 2.8}O{sub 8.0} with Sc-O distances of 214 - 230 pm. These octahedra are condensed via common edges and faces, encapsulating the In2Sc{sub 12} icosahedra. Due to the high scandium content one observes strong Sc-Sc bonding with Sc-Sc distances ranging from 303 to 362 pm in Sc{sub 49.2}Rh{sub 13}In{sub 3.8}O{sub 8.8}. The shortest distances occur for Sc-Rh (267 - 295 pm). The crystal chemical relationship with the Li{sub 3}Bi-related suboxide Ti{sub 12}Sn{sub 3}O{sub 10} is discussed. (orig.)

Human vaccination against RH5 induces neutralizing antimalarial antibodies that inhibit RH5 invasion complex interactions

DEFF Research Database (Denmark)

Payne, Ruth O; Silk, Sarah E; Elias, Sean C

2017-01-01

serum antibodies exhibited cross-strain functional growth inhibition activity (GIA) in vitro, targeted linear and conformational epitopes within RH5, and inhibited key interactions within the RH5 invasion complex. This is the first time to our knowledge that substantial RH5-specific responses have been...

Crystal structures of ZnCl2·2.5H2O, ZnCl2·3H2O and ZnCl2·4.5H2O

Directory of Open Access Journals (Sweden)

Erik Hennings

2014-12-01

Full Text Available The formation of different complexes in aqueous solutions is an important step in understanding the behavior of zinc chloride in water. The structure of concentrated ZnCl2 solutions is governed by coordination competition of Cl− and H2O around Zn2+. According to the solid–liquid phase diagram, the title compounds were crystallized below room temperature. The structure of ZnCl2·2.5H2O contains Zn2+ both in a tetrahedral coordination with Cl− and in an octahedral environment defined by five water molecules and one Cl− shared with the [ZnCl4]2− unit. Thus, these two different types of Zn2+ cations form isolated units with composition [Zn2Cl4(H2O5] (pentaaqua-μ-chlorido-trichloridodizinc. The trihydrate {hexaaquazinc tetrachloridozinc, [Zn(H2O6][ZnCl4]}, consists of three different Zn2+ cations, one of which is tetrahedrally coordinated by four Cl− anions. The two other Zn2+ cations are each located on an inversion centre and are octahedrally surrounded by water molecules. The [ZnCl4] tetrahedra and [Zn(H2O6] octahedra are arranged in alternating rows parallel to [001]. The structure of the 4.5-hydrate {hexaaquazinc tetrachloridozinc trihydrate, [Zn(H2O6][ZnCl4]·3H2O}, consists of isolated octahedral [Zn(H2O6] and tetrahedral [ZnCl4] units, as well as additional lattice water molecules. O—H...O hydrogen bonds between the water molecules as donor and ZnCl4 tetrahedra and water molecules as acceptor groups leads to the formation of a three-dimensional network in each of the three structures.

?????????? ?????, ?????????? ??????????? ?? ?????????? ?????????? ????? ? ?????? ???????? ZnCl2 +NH4Cl

OpenAIRE

Kuntyi, Orest; Zozulya, Galyna

2010-01-01

Zinc cementation by magnesium from ZnCl2 + NH4Cl aqueous solutions has been investigated. The amount of magnesium has been established as 0.8?2.0 g per 1 g of conditioned zinc to obtain recovery degree ? 99 %. At low concentrations of Zn2+ ions (0.025?0.1 M ZnCl2) dispersed deposit is formed with nanoparticles of reduced metal; at high concentrations (0.25?0.5 M) coarse-crystalline and fern-shaped deposit is formed. ?????????? ?????????? ????? ??????? ? ?????? ???????? ZnCl2 + NH4Cl. ????????...

Electrochemical corrosion behaviour of lead-free Sn-8.5 Zn-X Ag-0.1 Al-0.5 Ga solder in 3.5% NaCl solution

International Nuclear Information System (INIS)

Mohanty, Udit Surya; Lin, K.-L.

2005-01-01

The electrochemical corrosion behaviour of Pb-free Sn-8.5 Zn-X Ag-0.1 Al-0.5 Ga solder in 3.5% NaCl solution was investigated by using potentiodynamic polarization methods, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy (XPS) analysis. The results obtained from polarization studies showed that an increase in the Ag content from 0.1 to 1.5 wt% decreased the corrosion current density (I corr ) and shifted the corrosion potential (E corr ) towards more noble values. These changes were also reflected in the linear polarization resistance (LPR), corrosion rate, anodic Tafel slope (b A ) and the cathodic Tafel slope (b c ) values, respectively. Passivation behaviour was noted in the Sn-Zn-X Ag-Al-Ga solders with Ag content > 0.1 wt%. The oxides and hydroxides of zinc were responsible for the formation of passive film. Presence of Ag atoms in the oxide layer also improved the passivation behaviour of solders to a certain extent. X-ray photoelectron spectroscopy revealed that two different oxygen species were formed on the surface films, one was assigned to OH - in Zn(OH) 2 and the other to O 2 - in ZnO. XPS depth profile results revealed that the two species had different depth distribution in the films. SEM and EDX analyses confirmed SnCl 2 as the major corrosion product formed after the electrochemical experiments

Microstructural analysis nanoferritas Mn_0_,_5Zn_0_,_5Fe_2O_4 e Mn_0_,_6_5Zn_0_,_3_5Fe_2O_4 synthesized by combustion reaction

International Nuclear Information System (INIS)

Diniz, V.C.S.; Figueiredo, A.R.; Costa Junior, A.D.S.; Diniz, H.M.; Vieira, D.A.; Costa, A.C.F.M.

2014-01-01

The MnZn ferrites are ferrimagnetic materials that have been studied and used in various technological fields. In this work investigated the microstructural characteristics of ferrites and Mn_0_,_5Zn_0_,_5Fe_2O_4 Mn_0_,_6_5Zn_0_,_3_5Fe_2O_4 synthesized by combustion reaction in 200g scale production. The samples were characterized by XRD, crystallinity, crystallite size, X-ray fluorescence and scanning electron microscopy. Given the results it was observed that for both samples the synthesis combustion reaction was efficient for the production of single-phase ferrites with high crystallinity. With respect to the analysis of X-ray fluorescence was noted that the experimental values composition were consistent with the theoretical values calculated for both samples. Regarding morphology for both samples, the formation of the porous powders with feature consisting of dense clumps in the form of irregular foam was observed. (author)

Enterovirus inhibitory activity of C-8-tert-butyl substituted 4-aryl-6,7,8,9-tetrahydrobenzo[4,5]thieno[3,2-e][1,2,4]triazolo[4,3-a]pyrimidin-5(4H)-ones.

Science.gov (United States)

Kumar Biswas, Bishyajit; Malpani, Yashwardhan R; Ha, Neul; Kwon, Do-Hyun; Soo Shin, Jin; Kim, Hae-Soo; Kim, Chonsaeng; Bong Han, Soo; Lee, Chong-Kyo; Jung, Young-Sik

2017-08-01

Members of a series of 4-aryl-6,7,8,9-tetrahydrobenzo[4,5]thieno[3,2-e][1,2,4]triazolo[4,3-a]pyrimidin-5(4H)-ones (1, Fig. 2) were prepared and tested against representative enteroviruses including Human Coxsackievirus B1 (Cox B1), Human Coxsackievirus B3 (Cox B3), human Poliovirus 3 (PV3), human Rhinovirus 14 (HRV14), human Rhinovirus 21 (HRV 21) and human Rhinovirus 71 (HRV 71). The C-8-tert-butyl group on the tetrahydrobenzene ring in these substances was found to be crucial for their enterovirus activity. One member of this group, 1e, showed single digit micromolar activities (1.6-8.85μM) against a spectrum of viruses screened, and the highest selectivity index (SI) values for Cox B1 (>11.2), for Cox B3 (>11.5), and for PV3 (>51.2), respectively. In contrast, 1p, was the most active analog against the selected HRVs (1.8-2.6μM), and showed the highest selectivity indices among the group of compounds tested. The SI values for 1p were 11.5 for HRV14, 8.4 for HRV21, and 12.1 for HRV71, respectively. Copyright © 2017 Elsevier Ltd. All rights reserved.

Preparation, characterization and photocatalytic activity of visible-light-driven plasmonic Ag/AgBr/ZnFe2O4 nanocomposites

International Nuclear Information System (INIS)

Li, Xiaojuan; Tang, Duanlian; Tang, Fan; Zhu, Yunyan; He, Changfa; Liu, Minghua; Lin, Chunxiang; Liu, Yifan

2014-01-01

Highlights: • A plasmonic Ag/AgBr/ZnFe 2 O 4 photocatalyst has been successfully synthesized. • Ag/AgBr/ZnFe 2 O 4 nanocomposites exhibit high visible light photocatalytic activity. • Ag/AgBr/ZnFe 2 O 4 photocatalyst is stable and magnetically separable. - Abstract: A visible-light-driven plasmonic Ag/AgBr/ZnFe 2 O 4 nanocomposite has been successfully synthesized via a deposition–precipitation and photoreduction through a novel one-pot process. X-ray diffraction spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy and UV–vis diffuse reflectance spectroscopy were employed to investigate the crystal structure, chemical composition, morphology, and optical properties of the as-prepared nanocomposites. The photocatalytic activities of the nanocomposites were evaluated by photodegradation of Rhodamine B (RhB) and phenol under visible light. The results demonstrated that the obtained Ag/AgBr/ZnFe 2 O 4 nanocomposites exhibited higher photocatalytic activity as compared to pure ZnFe 2 O 4 . In addition, the sample photoreduced for 20 min and calcined at 500 °C achieved the highest photocatalytic activity. Furthermore, the Ag/AgBr/ZnFe 2 O 4 nanocomposite has high stability under visible light irradiation and could be conveniently separated by using an external magnetic field

Rapid microwave hydrothermal synthesis of ZnGa2O4 with high photocatalytic activity toward aromatic compounds in air and dyes in liquid water

International Nuclear Information System (INIS)

Sun Meng; Li Danzhen; Zhang Wenjuan; Chen Zhixin; Huang Hanjie; Li Wenjuan; He Yunhui; Fu Xianzhi

2012-01-01

ZnGa 2 O 4 was synthesized from Ga(NO 3 ) 3 and ZnCl 2 via a rapid and facile microwave-assisted hydrothermal method. The photocatalytic properties of the as-prepared ZnGa 2 O 4 were evaluated by the degradation of pollutants in air and aqueous solution under ultraviolet (UV) light illumination. The results demonstrated that ZnGa 2 O 4 had exhibited efficient photocatalytic activities higher than that of commercial P25 (Degussa Co.) in the degradation of benzene, toluene, and ethylbenzene, respectively. In the liquid phase degradation of dyes (methyl orange, Rhodamine B, and methylene blue), ZnGa 2 O 4 has also exhibited remarkable activities higher than that of P25. After 32 min of UV light irradiation, the decomposition ratio of methyl orange (10 ppm, 150 mL) over ZnGa 2 O 4 (0.06 g) was up to 99%. The TOC tests revealed that the mineralization ratio of MO (10 ppm, 150 mL) was 88.1% after 90 min of reaction. A possible mechanism of the photocatalysis over ZnGa 2 O 4 was also proposed. - Graphical abstract: In the degradation of RhB under UV light irradiation, ZnGa 2 O 4 had exhibited efficient photo-activity, and after only 24 min of irradiation the decomposition ratio was up to 99.8%. Highlights: ► A rapid and facile M–H method to synthesize ZnGa 2 O 4 photocatalyst. ► The photocatalyst exhibits high activity toward benzene and dyes. ► The catalyst possesses more surface hydroxyl sites than TiO 2 (P25). ► Deep oxidation of different aromatic compounds and dyes over catalyst.

(3-Methylbenzonitrile-κNtetrakis(μ-N-phenylacetamidato-κ4N:O;κ4O:N-dirhodium(II(Rh—Rh

Directory of Open Access Journals (Sweden)

Jennie Tan

2013-12-01

Full Text Available In the title compound, [Rh2(C8H8NO4(C8H7N], the four acetamidate ligands bridging the dirhodium core are arranged in a 2,2-trans manner. One RhII atom is five-coordinate, in a distorted pyramidal geometry, while the other is six-coordinate, with a disorted octahedral geometry. For the six-coordinate RhII atom, the axial nitrile ligand shows a non-linear Rh–nitrile coordination with an Rh—N—C bond angle of 166.4 (4° and a nitrile N—C bond length of 1.138 (6 Å. Each unique RhII atom is coordinated by a trans pair of N atoms and a trans pair of O atoms from the four acetamide ligands. The Neq—Rh—Rh—Oeq torsion angles on the acetamide bridge varies between 12.55 (11 and 14.04 (8°. In the crystal, the 3-methylbenzonitrile ring shows a π–π interaction with an inversion-related equivalent [interplanar spacing = 3.360 (6 Å]. A phenyl ring on one of the acetamide ligands also has a face-to-face π–π interaction with an inversion-related equivalent [interplanar spacing = 3.416 (5 Å].

Electrospinning direct synthesis of magnetic ZnFe{sub 2}O{sub 4}/ZnO multi-porous nanotubes with enhanced photocatalytic activity

Energy Technology Data Exchange (ETDEWEB)

Wang, Chunlei [College of Chemistry and Environmental Engineering, Wuhan Polytechnic University, Wuhan 430023 (China); Tan, Xing [College of Biology and Pharmaceutical Engineering, Wuhan Polytechnic University, Wuhan 430023 (China); Yan, Juntao, E-mail: yanjuntaonihao@163.com [College of Chemistry and Environmental Engineering, Wuhan Polytechnic University, Wuhan 430023 (China); Chai, Bo [College of Chemistry and Environmental Engineering, Wuhan Polytechnic University, Wuhan 430023 (China); Li, Jianfen, E-mail: lijfen@163.com [College of Chemistry and Environmental Engineering, Wuhan Polytechnic University, Wuhan 430023 (China); Chen, Shizhong [College of Food Science and Engineering, Wuhan Polytechnic University, Wuhan 430023 (China)

2017-02-28

Highlights: • ZnFe2O4/ZnO heterojunctions are firstly fabricated by electrospinning method. • ZnFe{sub 2}O{sub 4}/ZnO heterojunctions possess multi-porous nanotube structure. • ZnFe{sub 2}O{sub 4}/ZnO heterojunctions can significantly enhance photocatalytic activity. - Abstract: Magnetic ZnFe{sub 2}O{sub 4}/ZnO (ZFO/ZnO) multi-porous nanotubes have been first fabricated via a facile electrospinning and subsequent calcination process. A series of ZFO/ZnO photocatalysts with different ZFO molar content and morphologies are also obtained by varying the molar ratio of Zn/Fe metal salt and its dosage. The morphology, composition, crystal structure and specific surface area of achieved photocatalysts are systematically examined. TEM images demonstrate ZFO/ZnO-3 multi-porous nanotubes possess perfect 1D nanotube profile with hierarchical pores. HRTEM images confirm the formation of ZFO/ZnO heterojunctions. DRS spectra show that ZFO/ZnO-3 multi-porous nanotubes exhibit an enhanced absorption both in UV and visible-light region. PL spectra and photocurrent responses of ZFO/ZnO-3 multi-porous nanotube demonstrated that the photogenerated electrons and holes are effectively separated. Above all, ZFO/ZnO-3 multi-porous nanotubes photocatalysts with a larger specific surface area of 57.79 m{sup 2} g{sup −1} exhibit the best photocatalytic efficiency of 99% after 150 min under the solar irradiation for the decolorization of RhB. Moreover, ZFO/ZnO photocatalysts not only possess magnetic separation property, but also keep a relatively high photocatalytic efficiency even after four cycles, which is beneficial for practical application. In addition, both the formation and potential photocatalytic mechanisms of ZFO/ZnO-3 multi-porous nanotubes are proposed in detail.

Laser stimulated third harmonic generation studies in ZnO-Ta2O5-B2O3 glass ceramics entrenched with Zn3Ta2O8 crystal phases

Science.gov (United States)

Siva Sesha Reddy, A.; Jedryka, J.; Ozga, K.; Ravi Kumar, V.; Purnachand, N.; Kityk, I. V.; Veeraiah, N.

2018-02-01

In this study zinc borate glasses doped with different concentrations Ta2O5 were synthesized and were crystallized by heat treatment for prolonged times. The samples were characterized by XRD, SEM, IR and Raman spectroscopy techniques. The SEM images of the crystallized samples have indicated that the samples contain randomly distributed crystal grains with size ∼1 μm entrenched in the residual amorphous phase. XRD studies have exhibited diffraction peaks identified as being due to the reflections from (1 1 1) planes of monoclinic Zn3Ta2O8 crystal phase that contains intertwined tetrahedral zinc and octahedral tantalate structural units. The concentration of such crystal phases in the bulk samples is observed to increase with increase of Ta2O5 up to 3.0 mol%. The IR and Raman spectroscopy studies have confirmed the presence of ZnO4 and TaO6 structural units in the glass network in addition to the conventional borate structural units. For measuring third harmonic generation (THG) in the samples, the samples were irradiated with 532 nm laser beam and the intensity of THG of probing beam (Nd:YAG λ = 1064 nm 20 ns pulsed laser (ω)) is measured as a function of fundamental beam power varying up to 200 J/m2. The intensity of THG is found to be increasing with increase of fundamental beam power and found to be the maximal for the glass crystallized with 3.0 mol% of Ta2O5. The intensity of THG of the ceramicized samples is found to be nearly 5 times higher with respect to that of pre-crystallized samples. The generation of 3ω is attributed to the perturbation/interaction between Zn3Ta2O8 anisotropic crystal grains and the incident probing beam.

15 CFR 8b.4 - Discrimination prohibited.

Science.gov (United States)

2010-01-01

... 15 Commerce and Foreign Trade 1 2010-01-01 2010-01-01 false Discrimination prohibited. 8b.4 Section 8b.4 Commerce and Foreign Trade Office of the Secretary of Commerce PROHIBITION OF DISCRIMINATION... Provisions § 8b.4 Discrimination prohibited. (a) General. No qualified handicapped individual shall, on the...

B-Zell-Lymphome der Haut - Pathogenese, Diagnostik und Therapie.

Science.gov (United States)

Nicolay, Jan P; Wobser, Marion

2016-12-01

Primär kutane B-Zell-Lymphome (PCBCL) beschreiben reifzellige lymphoproliferative Erkrankungen der B-Zell-Reihe, die primär die Haut betreffen. Die Biologie und der klinische Verlauf der einzelnen PCBCL-Subtypen variieren untereinander stark und unterscheiden sich grundsätzlich von primär nodalen und systemischen B-Zell-Lymphomen. Primär kutane Marginalzonenlymphome (PCMZL) und primäre kutane follikuläre Keimzentrumslymphome (PCFCL) werden auf Grund ihres unkomplizierten Verlaufs und ihrer exzellenten Prognose zu den indolenten PCBCL gezählt. Demgegenüber stellen die diffus großzelligen B-Zell-Lymphome, hauptsächlich vom Beintyp (DLBCL, LT) die aggressiveren PCBCL-Varianten mit schlechterer Prognose dar. Für die Ausbreitungsdiagnostik und die Therapieentscheidung sind eine genaue histologische und immunhistochemische Klassifizierung sowie der Ausschluss einer systemischen Beteiligung in Abgrenzung zu nodalen oder systemischen Lymphomen notwendig. Die Diagnostik sollte dabei durch molekularbiologische Untersuchungen unterstützt werden. Therapeutisch stehen für die indolenten PCBCL primär operative und radioonkologische Maßnahmen im Vordergrund sowie eine Systemtherapie mit dem CD20-Antikörper Rituximab bei disseminiertem Befall. Die aggressiveren Varianten sollten in erster Linie mit Kombinationen aus Rituximab und Polychemotherapieschemata wie z. B. dem CHOP-Schema oder Modifikationen davon behandelt werden. Auf Grund der in allen seinen Einzelheiten noch nicht vollständig verstandenen Pathogenese und Biologie sowie des begrenzten Therapiespektrums der PCBCL besteht hier, speziell beim DLBCL, LT, noch erheblicher Forschungsbedarf. © 2016 Deutsche Dermatologische Gesellschaft (DDG). Published by John Wiley & Sons Ltd.

Two superstructures of Ce{sub 3}Rh{sub 4}Ge{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Vosswinkel, Daniel; Hoffmann, Rolf-Dieter [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie; Svitlyk, Volodymyr [European Synchrotron Radiation Facility, Grenoble (France); and others

2018-04-01

Two different samples of Ce{sub 3}Rh{sub 4}Ge{sub 4} were synthesized from different starting compositions by melting of the elements in an arc-melting furnace followed by annealing sequences in a sealed tantalum ampoule in a muffle furnace. The structures of two different stacking variants were refined on the basis of temperature dependent single-crystal X-ray diffractometer data. At high temperature Ce{sub 3}Rh{sub 4}Ge{sub 4} adopts the U{sub 3}Ni{sub 4}Si{sub 4} type structure with strongly enhanced anisotropic displacement parameters for the Rh1 atoms. For the two different crystals, additional reflections start to appear at different temperatures. The first crystal showed additional reflections already at room temperature (stacking variant I) and the second one showed additional reflections emerging below 270 K (stacking variant II). Stacking variant I could be described with the (3+1)D superspace group I2/m(α0γ)00; α=1/2a*, γ=1/2c*; (Z=2), 1252 F{sup 2} values, 48 variables, wR=0.0306 for the main and wR=0.0527 for 440 1{sup st} order satellite reflections, similar to Pr{sub 3}Rh{sub 4}Ge{sub 4}. For stacking variant II the (3+1)D superspace group is Immm(α00)00s; α=1/2a*; (Z=2). The structure could be refined with 1261 F{sup 2} values, 53 variables and residuals of wR=0.0331 for the main reflections and wR=0.1755 (R1{sub obs}=0.0788) for the 1{sup st} order satellite reflections, [a=406.2(1), b=423.7(1) and c=2497.1(1) pm]. The commensurate description could be transformed to a three-dimensional (3D) supercell with space group Pnma and Z=4: a=812.5(1), b=423.7(1), c=2497.1(2) pm, 1261 F{sup 2} values, 69 variables and wR=0.0525. The relation of the U{sub 3}Ni{sub 4}Si{sub 4} type structure, the (3+1)D modulated and the 3D supercells are discussed on the basis of group-subgroup schemes. Ab initio electronic structure calculations are in line with the diffraction experiments, revealing the lowest total energy for the Pnma phase.

Relationships between skin cancers and blood groups--link between non-melanomas and ABO/Rh factors.

Science.gov (United States)

Cihan, Yasemin Benderli; Baykan, Halit; Kavuncuoglu, Erhan; Mutlu, Hasan; Kucukoglu, Mehmet Burhan; Ozyurt, Kemal; Oguz, Arzu

2013-01-01

This investigation focused on possible relationships between skin cancers and ABO/Rh blood groups. Between January 2005 and December 2012, medical data of 255 patients with skin cancers who were admitted to Kayseri Training and Research Hospital, Radiation Oncology and Plastic Surgery Outpatient Clinics were retrospectively analyzed. Blood groups of these patients were recorded. The control group consisted of 25701 healthy volunteers who were admitted to Kayseri Training and Research Hospital, Blood Donation Center between January 2010 and December 2011. The distribution of the blood groups of the patients with skin cancers was compared to the distribution of ABO/Rh blood groups of healthy controls. The association of the histopathological subtypes of skin cancer with the blood groups was also investigated. Of the patients, 50.2% had A type, 26.3% had O type, 16.1% had B type, and 7.5% had AB blood group with a positive Rh (+) in 77.3%. Of the controls, 44.3% had A type, 31.5% had 0 type, 16.1% had B type, and 8.1% had AB blood group with a positive Rh (+) in 87.8%. There was a statistically significant difference in the distribution of blood groups and Rh factors (A Rh (-) and 0 Rh positive) between the patients and controls. A total of 36.8% and 20.4% of the patients with basal cell carcinoma (BCC) had A Rh (+) and B Rh (+), respectively, while 39.2% and 27.6% of the controls had A Rh (+) and B Rh (+), respectively. A significant relationship was observed between the patients with BCC and controls in terms of A Rh (-) (p=0.001). Our study results demonstrated that there is a significant relationship between non-melanoma skin cancer and ABO/Rh factors.

Ternary g-C{sub 3}N{sub 4}/ZnO/AgCl nanocomposites: Synergistic collaboration on visible-light-driven activity in photodegradation of an organic pollutant

Energy Technology Data Exchange (ETDEWEB)

Akhundi, Anise; Habibi-Yangjeh, Aziz, E-mail: ahabibi@uma.ac.ir

2015-12-15

Graphical abstract: - Highlights: • Novel ternary g-C{sub 3}N{sub 4}/ZnO/AgCl nanocomposites were prepared using a facile method. • g-C{sub 3}N{sub 4}/ZnO/AgCl (40%) has superior activity in degradation of RhB under visible-light. • The activity is 7.5 and 6-fold higher than g-C{sub 3}N{sub 4}/ZnO and g-C{sub 3}N{sub 4}/AgCl, respectively. • There are synergistic collaboration between ZnO and AgCl in enhancing the activity. - Abstract: The present work demonstrates the preparation of ternary g-C{sub 3}N{sub 4}/ZnO/AgCl nanocomposites, as novel visible-light-driven photocatalysts, using a facile large-scale methodology. The microstructure, morphology, purity, thermal, and spectroscopic properties of the prepared samples were studied using XRD, TEM, EDX, TG, UV–vis DRS, FT-IR, and PL techniques. Compared with the g-C{sub 3}N{sub 4}/ZnO and g-C{sub 3}N{sub 4}/AgCl nanocomposites, the g-C{sub 3}N{sub 4}/ZnO/AgCl nanocomposites displayed higher photocatalytic activity for degradation of rhodamine B under visible-light irradiation. Photocatalytic activity of the g-C{sub 3}N{sub 4}/ZnO/AgCl (40%) nanocomposite is about 9.5, 7.5, and 6-fold higher than those of the g-C{sub 3}N{sub 4}, g-C{sub 3}N{sub 4}/ZnO, and g-C{sub 3}N{sub 4}/AgCl samples, respectively. The enhanced photocatalytic activity of the nanocomposites was mainly attributed to efficiently separation of the charge carriers by synergistic collaboration of ZnO and AgCl in removing photogenerated electrons from g-C{sub 3}N{sub 4}. Furthermore, the results showed that the photocatalytic activity of the nanocomposite considerably depends on the preparation time, calcination temperature, and scavengers of the reactive species. Finally, the nanocomposite was found to be a reusable photocatalyst.

Preparation and property of magnetic photocatalyst BiOCl/Mn{sub x}Zn{sub 1−x}Fe{sub 2}O{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Feng, Shan; Xu, Longjun, E-mail: xulj@cqu.edu.cn; Liu, Chenglun [State Key Laboratory of Coal Mine Disaster Dynamics and Control (China); Du, Haigang [Liupanshui Normal University, Department of Mining Engineering (China); Xie, Taiping [State Key Laboratory of Coal Mine Disaster Dynamics and Control (China); Zhu, Qianqian [Chongqing University, College of Chemistry and Chemical Engineering (China)

2017-02-15

The magnetic photocatalyst BiOCl/Mn{sub x}Zn{sub 1−x}Fe{sub 2}O{sub 4} was prepared by impregnation-calcination method. The structure and properties of the prepared photocatalyst were characterized by FTIR, XRD, SEM, TEM, UV–vis DRS, and VSM. Mn{sub x}Zn{sub 1−x}Fe{sub 2}O{sub 4} inhibited the growth along (001) crystal face and promoted (110) crystal surface exposure of BiOCl. The as-prepared magnetic composite appeared flower-like microspheres assembled with nanosheets. The average crystallite size and the nanosheet thickness range of BiOCl/Mn{sub x}Zn{sub 1−x}Fe{sub 2}O{sub 4} were 57.6 and 75.7–112.2 nm, respectively. The band gap energy (E{sub g}) of BiOCl/Mn{sub x}Zn{sub 1−x}Fe{sub 2}O{sub 4} was 2.48 eV, which was lower than that of BiOCl. The saturation magnetization (Ms), coercive force (Hc), and remanent magnetization (Mr) of BiOCl/Mn{sub x}Zn{sub 1−x}Fe{sub 2}O{sub 4} were respectively 4.64 emu g{sup −1}, 50.12 G and 0.09 emu g{sup −1}, indicating a good resistance to demagnetization and paramagnetism. The optimum synthesis condition of BiOCl/Mn{sub x}Zn{sub 1−x}Fe{sub 2}O{sub 4} was obtained by orthogonal experiments, and the degradation ratio of RhB with the photocatalyst was 99.6% at 30 min. After four cycles, the degradation ratio of RhB with the recovered photocatalyst was still above 83%.

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

Directory of Open Access Journals (Sweden)

Maya Markova-Velichkova

2009-12-01

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

A re-evaluation of k sub 0 and related nuclear data for the 555.8 keV gamma-line emitted by the sup 1 sup 0 sup 4 sup m Rh- sup 1 sup 0 sup 4 Rh mother-daughter pair for use in NAA

CERN Document Server

Corte, F D; Simonits, A; Bossus, D; Sluijs, R V; Pommé, S

1999-01-01

A re-evaluation is made of the k sub 0 -factor and related nuclear data for the 555.8 keV gamma-ray of the sup 1 sup 0 sup 4 sup m Rh- sup 1 sup 0 sup 4 Rh mother-daughter pair that are important in neutron activation analysis (NAA). This study considers that the relevant level is also fed by the 4.34 min sup 1 sup 0 sup 4 sup m Rh mother (with an absolute gamma-ray emission probability gamma sub 2 =0.13%) and not only, as assumed in former work, by the 42.3 s sup 1 sup 0 sup 4 Rh daughter isotope (with gamma sub 3 =2.0%). In view of this, generalised equations were developed for both the experimental determination and the analytical use of the k sub 0 -factor and of the associated parameters k sub 0 (m)/k sub 0 (g), Q sub 0 (m) and Q sub 0 (g) [(m): sup 1 sup 0 sup 4 sup m Rh; (g): sup 1 sup 0 sup 4 Rh], requiring the introduction of the gamma sub 2 and gamma sub 3 data and also of the sup 1 sup 0 sup 4 sup m Rh-> sup 1 sup 0 sup 4 Rh fractional decay factor F sub 2 (=0.9987). The experimental determinations...

Influences of Gd on the microstructure and strength of Mg-4.5Zn alloy

International Nuclear Information System (INIS)

Yang Jie; Xiao Wenlong; Wang Lidong; Wu Yaoming; Wang Limin; Zhang Hongjie

2008-01-01

Microstructure and mechanical properties of peak-aged Mg-4.5Zn-xGd (x 0, 0.5, 1.0 and 1.5 wt.%) alloys have been investigated. The results showed that the grain size of the alloys was refined gradually with increasing Gd. Mg 5 Gd and Mg 3 Gd 2 Zn 3 phases were found in the Gd-containing alloys. The strengths were greatly improved with Gd additions, and the highest strength level was obtained in the Mg-4.5Zn-1.5Gd alloy, in which the ultimate tensile strength and yield strength were 231 MPa and 113 MPa, respectively. Through comparing with the Mg-4.5Zn alloy, the increments of ultimate tensile strength and yield strength were 22 MPa and 56 MPa, respectively. The improved strength was mainly correlated to the grain refining effect, the strengthening effect of the Mg 5 Gd and Mg 3 Gd 2 Zn 3 phases and also the hardening effect of the solutioned Gd atoms

Distribution of ABO/Rh blood groups and their association with hepatitis B virus infection in 3.8 million Chinese adults: A population-based cross-sectional study.

Science.gov (United States)

Liu, J; Zhang, S; Liu, M; Wang, Q; Shen, H; Zhang, Y

2018-04-01

ABO and Rh blood groups play a vital role in blood transfusion safety and clinical practice and are thought to be linked with disease susceptibility. The results from previous studies that focused on the association between blood groups and HBV infection remain controversial. China has the world's largest burden of HBV infection. We assessed the distribution of ABO/Rh blood groups in Chinese adults and examined the association between these groups and HBV infection. We did a nationwide cross-sectional study using data from a physical check-up programme from 31 provinces examined between 2010 and 2012. ELISA was used to test for HBsAg in serologic samples. Multivariable logistic regression was used to estimate aOR of the association between ABO and Rh blood groups and HBV infection. Among 3 827 125 participants, the proportion of participants with blood group A was highest (30.54%), followed by O (30.37%), B (29.42%) and AB (9.66%). A total of 38 907 (1.02%) were Rh-D negative. The prevalence of HBsAg in blood groups O, A, B and AB were 6.34%, 5.55%, 5.18% and 5.06%, respectively. HBsAg prevalence was 5.65% in Rh-D-positive and 3.96% in Rh-D-negative participants. After controlling for other potential risk factors, multivariate models showed that participants with blood group O (adjusted OR = 1.22, 95% CI: 1.20-1.25) were at higher risk of HBV infection compared with group AB. Rh-D-positive participants (adjusted OR = 1.44, 95% CI: 1.37-1.52) were at higher risk of HBV infection than Rh-D-negative participants. The associations between ABO/Rh blood groups and HBV infection were similar in subgroup analysis. The proportions of O, A, B and AB blood groups were approximately 3:3:3:1, and nearly 1 in 100 people was Rh-D negative among Chinese adults. Blood group O and Rh-D positivity were both associated with increased HBV infection. The risk of HBV infection and blood safety should be taken into consideration in clinical practice, especially when transfusing

Novel ternary composites: Preparation, performance and application of ZnFe2O4/TiO2/polyaniline

Science.gov (United States)

Li, Juanbi; Xiao, Qiushi; Li, Liangchao; Shen, Junhai; Hu, Diqiong

2015-03-01

A series of ZnFe2O4/TiO2/polyaniline ternary composites with excellent photocatalytic activity were successfully synthesized by chemical method. The phase composition, morphology, conductivity, electrical and magnetic performances of the as-samples were characterized by means of modern measurement technology. And the photocatalytic degradation activity tests for the samples were estimated using rhodamine B (RhB) and methyl orange (MO) as targeted pollutants. The results indicated that there existed some interactions between each component in the ternary composites, and the electrical conductivities and photocatalytic degradation activities of the ternary composites were improved due to the coating of polyaniline. Moreover, when the mass fraction of aniline was up to 50%, the ternary composite exhibited a great decontaminating (including photocatalytic degradation and adsorption) activity of on both MO and RhB and displayed an excellent reusability.

Removal of Organic Dyes by Nanostructure ZnO-Bamboo Charcoal Composites with Photocatalysis Function

Directory of Open Access Journals (Sweden)

Xinliang Yu

2015-01-01

Full Text Available Composites of nanostructure zinc oxide (nano-ZnO and bamboo charcoal (BC were successfully prepared via impregnation-precipitation method. The products were characterized by XRD, SEM, and EDS. Rhodamine B (RhB and acid fuchsin (AF were selected as the organic dyes of photocatalysis degradation under the irradiation of ultraviolet light (UV. The influence of particle size of BC, irradiation time, pH value of the solution, and additive amount of H2O2 on removal of the dyes has been studied. The results show that smaller particle size of BC in the composites has a better removal effect. The composites possess the highest removal capacity for RhB and AF under the conditions of pH = 2 and pH = 5.4, respectively. The optimum additive amount of H2O2 for 5 mL RhB and AF was 0.050 mL and 0.1 mL, with a removal rate of 93% and 99%, respectively.

A low temperature situ precipitation route to designing Zn-doped SnO2 photocatalyst with enhanced photocatalytic performance

International Nuclear Information System (INIS)

Jia, Xiaohua; Liu, Yingying; Wu, Xiangyang; Zhang, Zhen

2014-01-01

Highlights: • A new Zn doped SnO 2 photocatalyst was successfully achieved and characterized. • The Zn doped SnO 2 photocatalyst exhibited excellent photocatalytic activity and stability for the photodegradation RhB. • Photocatalytic mechanisms both under visible and UV–vis light irradiation were proposed. - Abstract: Zn doped SnO 2 nanoparticles have been fabricated through the low temperature situ precipitation technique. The morphology, structure and chemical composition of the nanoparticles are characterized using field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), UV–vis diffuse reflectance spectroscopy (DRS), Thermogravimetric-differential scanning calorimetry (TG–DSC) and UV–vis absorption spectroscopy. The products were also characterized by X-ray diffraction (XRD) and X-photoelectron spectrum (XPS), and the results indicated that Sn 4+ ions were successfully substituted by Zn 2+ . Their photocatalytic activities were evaluated using rhodamine B (RhB) as a decomposition objective. The results show that the Zn doped SnO 2 display higher photocatalytic activities in the degradation of RhB than pure ZnO products by exposure to UV irradiation. A possible reason of the increased photocatalytic activity of Zn doped SnO 2 is attributed to intrinsic oxygen vacancies in nanoparticles and extrinsic defect due to Zn hole doping

Duplicaat 24-uurs voedingen 1994, inname aan zink

NARCIS (Netherlands)

Loon JW van; Ooik A van; Ritsema R; LAC

1997-01-01

Voor het onderzoek naar de dagelijkse inname aan zink via de voeding, inclusief drank en drinkwater werden 123 duplicaten van 24-uurs voedingen verzameld in de regio Utrecht. Twee groepen vrijwilligers werden geselecteerd die, sociaal en qua leeftijd, een zo getrouw mogelijk beeld vormden van de

Aanvoer koper en zink erg hoog op melkveebedrijven

NARCIS (Netherlands)

Smolders, E.A.A.; Verkaik, J.C.; Middelkoop, van J.C.

2006-01-01

De Europese kaderrichtlijn Water bepaalt dat de kwaliteit van het oppervlaktewater in 2015 zodanig verbeterd moet zijn, dat dit geen problemen meer oplevert voor het waterleven en voor het gebruik als drinkwater. Voor Nederland betekent dit onder andere dat de uitspoeling van koper en zink uit de

Two new three-dimensional zinc phosphites templated by piperazine: [H2pip][Zn3(HPO3)4(H2O)2] and K[H2pip]0.5[Zn3(HPO3)4

Science.gov (United States)

Zhang, Xiao; Wang, Guo-Ming; Wang, Zong-Hua; Wang, Ying-Xia; Lin, Jian-Hua

2014-01-01

Two three-dimensional open-framework zinc phosphites with the same organically templated, [H2pip][Zn3(HPO3)4(H2O)2] (1) and K[H2pip]0.5[Zn3(HPO3)4] (2) (pip = piperazine), have been solvothermally synthesized and structurally characterized by IR, elemental analysis, thermogravimetric analysis, powder and single-crystal X-ray diffractions. Compound 1 consists of ZnO4 tetrahedra, [HPO3] pseudopyramids and [ZnO4(H2O)2] octahedra, which are linked through their vertexes to generate three-dimensional architecture with intersecting 8-membered channels along the [1 0 0], [0 0 1] and [1 0 1] directions. Compound 2 is constructed from strictly alternating ZnO4 tetrahedra and [HPO3] pseudopyramids, and exhibits (3,4)-connected inorganic framework with 8-, and 12-membered channels, in which the K+ and diprotonated H2pip2+ extra-framework cations reside, respectively. The coexistence of inorganic K+ and organic piperazine mixed templates in the structure is unique and, to the best of our knowledge, firstly observed in metal-phosphite materials. In addition, the participation of left-handed and right-handed helical chains in construction of the puckered 4.82 sheet structure in 2 is also noteworthy.

Synthesis, DNA binding and cytotoxic activity of pyrimido[4',5':4,5]thieno(2,3-b)quinoline with 9-hydroxy-4-(3-diethylaminopropylamino) and 8-methoxy-4-(3-diethylaminopropylamino) substitutions.

Science.gov (United States)

KiranKumar, Hulihalli N; RohitKumar, Heggodu G; Advirao, Gopal M

2018-01-01

Two new derivatives of pyrimido[4',5';4,5]thieno(2,3-b)quinoline (PTQ), 9-hydroxy-4-(3-diethylaminopropylamino)pyrimido[4',5';4,5]thieno(2,3-b)quinoline (Hydroxy-DPTQ) and 8-methoxy-4-(3-diethylaminopropylamino)pyrimido[4',5';4,5]thieno(2,3-b)quinoline (Methoxy-DPTQ) were synthesized and their DNA binding ability was analyzed using spectroscopy (UV-visible, fluorescence and circular dichroism), ethidium bromide dye displacement assay, melting temperature (T m ) analysis and computational docking studies. The hypochromism in UV-visible spectrum and increased fluorescence emission of Hydroxy-DPTQ and Methoxy-DPTQ in the presence of DNA suggested the molecule-DNA interaction. The association constants calculated from UV-visible and spectral titrations were of the order 10 4 to 10 6 M -1 . Circular dichroism studies corroborated the induced conformational changes in DNA upon addition of molecules. The change in the ellipticity was observed both in negative and positive peak of DNA, thus, suggesting the intercalation of molecules. The observed displacement of ethidium bromide from the DNA and increased T m , upon addition of DNA confirmed the intercalative mode of binding. This was further validated by computational docking, which showed clear intercalation of molecules into the d(GpC)-d(CpG) site of the receptor DNA. Anticancer activities of these molecules are evaluated by using MTT assay. Both molecules showed antiproliferative activity against all the three cancer cells studied, with Hydroxy-DPTQ being more potential molecule among the two. IC 50 value of Hydroxy-DPTQ and Methoxy-DPTQ were in the range of 3-5μM and 130-250μM, respectively. Copyright © 2017 Elsevier B.V. All rights reserved.

Study of coexistence of ferromagnetism and superconductivity in single-crystal ErRh4B4

International Nuclear Information System (INIS)

Sinha, S.K.; Crabtree, G.W.; Hinks, D.G.; Mook, H.

1981-01-01

Neutron diffraction and resistivity measurements on single crystals of ErRh 4 B 4 have revealed that both superconductivity and ferromagnetic order coexist in this material between 0.71 and 1.2 0 K. In this intermediate phase, a linear polarized modulated structure with a wavelength of approximately 100 A is observed. The modulated moment increases faster than the ferromagnetic moment down to 0.71 K and then disappears suddenly, with loss of superconductivity and a transition to a normal ferromagnetic state. This transition is accompanied by temperature hysteresis of about 60 mK. The same hysteresis, in the inverse sense, is exhibited by the ferromagnetic component. We interpret the intermediate phase as being one of coexisting normal ferromagnetic domains and superconducting sinusoidally ordered domains. Evidence of a small percentage of small ferromagnetic regions of size approx. 100 A is also seen in both the intermediate and ferromagnetic phases. 3 figures

Growth and Characterization of Organic Marine Dye Compound: 6-Amino-8α-methoxy-5-methyl-4,7-dioxo-1,1a, 2,4,7,8,8a,8b-octahydroazireno[2',3':3,4] pyrrolo[1,2-α]indol- 8-yl]methyl Carbamate

OpenAIRE

Jayandran, M.; Balasubramanian, V.

2011-01-01

Single crystals of 6-amino-8α-methoxy-5-methyl-4,7-dioxo-1,1a, 2,4,7,8,8a,8b-octahydroazireno[2',3':3,4]pyrrolo[1,2-α]indol-8-yl]methyl carbamate (Mitomycin), an organic marine dye material has been grown from solution by slow evaporation at ambient temperature. The growth of crystals has been carried out at various pH values and the growth was confirmed at pH 6. The chemical composition of the grown crystals was determined by the FTIR spectra. The crystalline nature and its various planes of...

Magnetic ordering and electrical resistivity in Co{sub 0.2}Zn{sub 0.8}Fe{sub 2}O{sub 4} spinel oxide

Energy Technology Data Exchange (ETDEWEB)

Bhowmik, R.N. [Experimental Condensed Matter Physics Division, Saha Institute of Nuclear Physics, 1/AF, Bidhannagar, Kolkata 700065 (India)], E-mail: rabindranath.bhowmik@saha.ac.in; Ranganathan, R. [Experimental Condensed Matter Physics Division, Saha Institute of Nuclear Physics, 1/AF, Bidhannagar, Kolkata 700065 (India); Ghosh, B.; Kumar, S. [Department of Physics, Jadavpur University, Kolkata 700 032 (India); Chattopadhyay, S. [Department of Physics, University of Calcutta, 92, A.P.C. Road, Kolkata 700009 (India)

2008-05-29

We report the magnetic, Moessbauer spectroscopy and resistivity measurements in order to understand the electronic behaviour of bulk Co{sub 0.2}Zn{sub 0.8}Fe{sub 2}O{sub 4} spinel oxide. The effect of magnetic order on electrical behaviour is observed from the resistivity measurements in the absence and presence of magnetic field. The analysis of Moessbauer spectra suggests the absence of Fe{sup 2+} ions in the system, which implies that complete hopping of charge carriers between localized Fe{sup 3+}/Co{sup 2+} and Fe{sup 2+}/Co{sup 3+} pair of ions in B sublattice is not the favourable mechanism in Co{sub 0.2}Zn{sub 0.8}Fe{sub 2}O{sub 4}. We suggest that electrical behaviour of the present sample may be consistent with a model of fractional charge transfer via Fe{sub B}{sup 3+}-O{sup 2-}-Co{sub B}{sup 2+} superexchange path.

Fabrication and magnetic properties of Ni0.5Zn0.5Fe2O4 nanofibres by electrospinning

International Nuclear Information System (INIS)

Jun, Xiang; Xiang-Qian, Shen; Fu-Zhan, Song; Ming-Quan, Liu

2009-01-01

NiZn ferrite/polyvinylpyrrolidone composite fibres were prepared by sol–gel assisted electrospinning. Ni 0.5 Zn 0.5 Fe 2 O 4 nanofibres with a pure cubic spinel structure were obtained subsequently by calcination of the composite fibres at high temperatures. This paper investigates the thermal decomposition process, structures and morphologies of the electrospun composite fibres and the calcined Ni 0.5 Zn 0.5 Fe 2 O 4 nanofibres at different temperatures by thermo-gravimetric and differential thermal analysis, x-ray diffraction, Fourier transform infrared spectroscopy and field emission scanning electron microscopy. The magnetic behaviour of the resultant nanofibres was studied by a vibrating sample magnetometer. It is found that the grain sizes of the nanofibres increase significantly and the nanofibre morphology gradually transforms from a porous structure to a necklace-like nanostructure with the increase of calcination temperature. The Ni 0.5 Zn 0.5 Fe 2 O 4 nanofibres obtained at 1000 °C for 2 h are characterized by a necklace-like morphology and diameters of 100–200 nm. The saturation magnetization of the random Ni 0.5 Zn 0.5 Fe 2 O 4 nanofibres increases from 46.5 to 90.2 emu/g when the calcination temperature increases from 450 to 1000 °C. The coercivity reaches a maximum value of 11.0 kA/m at a calcination temperature of 600 °C. Due to the shape anisotropy, the aligned Ni 0.5 Zn 0.5 Fe 2 O 4 nanofibres exhibit an obvious magnetic anisotropy and the ease magnetizing direction is parallel to the nanofibre axis. (condensed matter: structure, thermal and mechanical properties)

Synthesis, structure and electronic configuration of [Rh{sub 6}Te{sub 8}(PPh{sub 3}){sub 6}].4C{sub 6}H{sub 6}

Energy Technology Data Exchange (ETDEWEB)

Thiele, Guenther; Balmer, Markus [Marburg Univ. (Germany). Fachbereich Chemie; Dehnen, Stefanie [Marburg Univ. (Germany). Fachbereich Chemie and Wissenschaftliches Zentrum fuer Materialwissenschaften

2016-08-01

[Rh{sub 6}Te{sub 8}(PPh{sub 3}){sub 6}].4C{sub 6}H{sub 6}, the first compound with a molecular Chevrel-type [Rh{sub 6}Te{sub 8}] cluster core has been synthesized and structurally characterized. By means of quantum chemical calculation, the close relationship of its electronic configuration to that of the lighter homologue has been demonstrated. The different crystal solvent content prevents an isostructural crystallization.

Isolation and X-ray structures of four Rh(PCP) complexes including a Rh(I) dioxygen complex with a short O-O bond

KAUST Repository

Hayashi, Yukiko

2013-07-01

The reaction of RhCl3·H2O with tBu2P(CH2)5PtBu 2 afforded several complexes including [RhIII(H)Cl{ tBu2- P(CH2)2CH(CH2) 2PtBu2}] (1), [RhIIIHCl 2{tBu2P(CH2)5P tBu2}]2 (2), [RhICl{ tBu2P(CH2)2CH=CHCH2P tBu2}] (3) and [RhICl{tBu 2PCH2C(O)CH=CHCH2PtBu2}] (4). X-ray crystal structures of 3 and 4 showed that the C=C bond on the C 5 unit of tBu2P(CH2) 5PtBu2 is bound to Rh(I) in a η2 configuration. In 4, the Rh atom has a trigonal pyramidal coordination geometry. The X-ray crystal structure of 2 consists of two rhodium( III) centers bridged by two tBu2P(CH2)5P tBu2 ligands with two phosphorus atoms, one from each ligand, trans to one another. The crystal structure of the rhodium oxygen adduct with 1,3-bis(di-t-butylphosphinomethyl) benzene [RhO2{ tBu2PCH2(C6H3)CH 2PtBu2}] (5) was also investigated. In this species the O2 is η2 coordinated to the Rh(I) center with asymmetric Rh-O bond lengths (2.087(7) and 1.998(8) Å). The O-O bond distance is short (1.337(11) Å) with νO-O of 990.5 cm -1. DFT calculations on complex 5 yielded two η2- O2 structures that differed in energy by only 0.76 kcal/mol. The lower energy one (5a) had near C2 symmetry, and had nearly equal Rh-O bond lengths, while the higher energy structure (5b) had near Cs symmetry and generally good agreement with the experimental structure. The calculated UV-Vis and IR spectra of complex 5 are in excellent agreement with experiment. © 2012 Elsevier Ltd. All rights reserved.

Isolation and X-ray structures of four Rh(PCP) complexes including a Rh(I) dioxygen complex with a short O-O bond

KAUST Repository

Hayashi, Yukiko; Szalda, David J.; Grills, David C.; Hanson, Jonathan C.; Huang, Kuo-Wei; Muckerman, James T.; Fujita, Etsuko

2013-01-01

The reaction of RhCl3·H2O with tBu2P(CH2)5PtBu 2 afforded several complexes including [RhIII(H)Cl{ tBu2- P(CH2)2CH(CH2) 2PtBu2}] (1), [RhIIIHCl 2{tBu2P(CH2)5P tBu2}]2 (2), [RhICl{ tBu2P(CH2)2CH=CHCH2P tBu2}] (3) and [RhICl{tBu 2PCH2C(O)CH=CHCH2PtBu2}] (4). X-ray crystal structures of 3 and 4 showed that the C=C bond on the C 5 unit of tBu2P(CH2) 5PtBu2 is bound to Rh(I) in a η2 configuration. In 4, the Rh atom has a trigonal pyramidal coordination geometry. The X-ray crystal structure of 2 consists of two rhodium( III) centers bridged by two tBu2P(CH2)5P tBu2 ligands with two phosphorus atoms, one from each ligand, trans to one another. The crystal structure of the rhodium oxygen adduct with 1,3-bis(di-t-butylphosphinomethyl) benzene [RhO2{ tBu2PCH2(C6H3)CH 2PtBu2}] (5) was also investigated. In this species the O2 is η2 coordinated to the Rh(I) center with asymmetric Rh-O bond lengths (2.087(7) and 1.998(8) Å). The O-O bond distance is short (1.337(11) Å) with νO-O of 990.5 cm -1. DFT calculations on complex 5 yielded two η2- O2 structures that differed in energy by only 0.76 kcal/mol. The lower energy one (5a) had near C2 symmetry, and had nearly equal Rh-O bond lengths, while the higher energy structure (5b) had near Cs symmetry and generally good agreement with the experimental structure. The calculated UV-Vis and IR spectra of complex 5 are in excellent agreement with experiment. © 2012 Elsevier Ltd. All rights reserved.

Quasi-two-dimensional Fermi-liquid state in Sr2RhO4-δ

International Nuclear Information System (INIS)

Nagai, Ichiro; Shirakawa, Naoki; Umeyama, Norio; Ikeda, Shin-ichi

2010-01-01

Single crystals of layered perovskite Sr 2 RhO 4-δ (δ=0.0 and 0.1) are successfully grown by the floating-zone method. Stoichiometric single crystals (Sr 2 RhO 4.0 ) are obtained by O 2 -annealing the as-grown crystals (Sr 2 RhO 3.9 ). Sr 2 RhO 4.0 and Sr 2 RhO 3.9 show quasi-two-dimensional Fermi-liquid behavior at low temperatures, whereas there are large differences in the anisotropy of electrical resistivity ρ c (3 K)/ρ ab (3 K) and Wilson ratio R w between Sr 2 RhO 4.0 and Sr 2 RhO 3.9 : ρ c (3 K)/ρ ab (3 K)=2400 (19000) and R w =3.8 (6.4) for Sr 2 RhO 4.0 (Sr 2 RhO 3.9 ). The differences observed between the temperature dependence of the in-plane electrical resistivity (T 2 RhO 4.0 and Sr 2 RhO 3.9 are mainly derived from those between the density of states and band structure near the corresponding Fermi level. This indicates that the changes in these physical properties, which are accompanied by oxygen defects in the Sr 2 RhO 4-δ system, can be explained by the rigid band model. Moreover, these results suggest that t 2g band-filling can be controlled by adjusting the oxygen defect content δ in the Sr 2 RhO 4-δ system. Although many similarities are observed in this study between the physical properties of Sr 2 RhO 4.0 and Sr 2 RuO 4 . Sr 2 RhO 4.0 does not exhibit superconductivity down to 36 mK. (author)

Structural evolution of the double perovskites Sr{sub 2}B'UO{sub 6} (B' = Mn, Fe, Co, Ni, Zn) upon reduction: Magnetic behavior of the uranium cations

Energy Technology Data Exchange (ETDEWEB)

Pinacca, R.M., E-mail: rmp@unsl.edu.ar [Area de Quimica General e Inorganica ' Dr. Gabino F. Puelles' , Departamento de Quimica, Facultad de Quimica, Bioquimica y Farmacia, Universidad Nacional de San Luis, Chacabuco y Pedernera, 5700 San Luis (Argentina); Viola, M.C.; Pedregosa, J.C. [Area de Quimica General e Inorganica ' Dr. Gabino F. Puelles' , Departamento de Quimica, Facultad de Quimica, Bioquimica y Farmacia, Universidad Nacional de San Luis, Chacabuco y Pedernera, 5700 San Luis (Argentina); Carbonio, R.E. [INFIQC (CONICET), Departamento de Fisicoquimica, Facultad de Ciencias Quimicas, Universidad Nacional de Cordoba, Ciudad Universitaria, X5000HUA Cordoba (Argentina); Lope, M.J. Martinez; Alonso, J.A. [Instituto de Ciencia de Materiales de Madrid, C.S.I.C., Cantoblanco, 28049 Madrid (Spain)

2011-11-15

Highlights: {yields} Evolution of the double perovskites Sr{sub 2}B'UO{sub 6} upon reduction were studied by XRPD. {yields} Orthorhombic (Pnma) disordered perovskites SrB'{sub 0.5-x}U{sub 0.5+x}O{sub 3} were obtained at 900 {sup o}C. {yields} U{sup 5+/4+} and Zn{sup 2+} cations are distributed at random over the octahedral positions. {yields} AFM ordering for the perovskite with B' = Zn appears below 30 K. -- Abstract: We describe the preparation of five perovskite oxides obtained upon reduction of Sr{sub 2}B'UO{sub 6} (B' = Mn, Fe, Co, Ni, Zn) with H{sub 2}/N{sub 2} (5%/95%) at 900 {sup o}C during 8 h, and their structural characterization by X-ray powder diffraction (XRPD). During the reduction process there is a partial segregation of the elemental metal when B' = Co, Ni, Fe, and the corresponding B'O oxide when B' = Mn, Zn. Whereas the parent, oxygen stoichiometric double perovskites Sr{sub 2}B'UO{sub 6} are long-range ordered concerning B' and U cations. The crystal structures of the reduced phases, SrB'{sub 0.5-x}U{sub 0.5+x}O{sub 3} with 0.37 < x < 0.27, correspond to simple, disordered perovskites; they are orthorhombic, space group Pnma (No. 62), with a full cationic disorder at the B site. Magnetic measurements performed on the phase with B' = Zn, indicate uncompensated antiferromagnetic ordering of the U{sup 5+}/U{sup 4+} sublattice below 30 K.

Mean-field theory for the Tsub(c2)-minimum in the phase diagram of Ersub(1-x)Hosub(x)Rh4B4

International Nuclear Information System (INIS)

Schuh, B.; Grewe, N.

1981-01-01

The experimentally observed shape of the phase boundary between the superconducting and the ferromagnetically ordered state in the reentrant ferromagnetic superconductor compound Ersub(1-x)Hosub(x)Rh 4 B 4 is explained within a simple Ginsburg-Landau mean field theory as resulting from a competition of two order parameters corresponding to the magnetic Ho- and Er-moments respectively. (author)

UV Light-Driven Photodegradation of Methylene Blue by Using Mn0.5Zn0.5Fe2O4/SiO2 Nanocomposites

Science.gov (United States)

Indrayana, I. P. T.; Julian, T.; Suharyadi, E.

2018-04-01

The photodegradation activity of nanocomposites for 20 ppm methylene blue solution has been investigated in this work. Nanocomposites Mn0.5Zn0.5Fe2O4/SiO2 have been synthesized using coprecipitation method. The X-ray diffraction (XRD) pattern confirmed the formation of three phases in sample Mn0.5Zn0.5Fe2O4/SiO2 i.e., Mn0.5Zn0.5Fe2O4, Zn(OH)2, and SiO2. The appearance of SiO2 phase showed that the encapsulation process has been carried out. The calculated particles size of Mn0.5Zn0.5Fe2O4/SiO2 is greater than Mn0.5Zn0.5Fe2O4. Bonding analysis via vibrational spectra for Mn0.5Zn0.5Fe2O4/SiO2 confirmed the formation of bonds Me-O-Si stretching (2854.65 cm-1) and Si-O-Si asymmetric stretching (1026.13 cm-1). The optical gap energy of Mn0.5Zn0.5Fe2O4/SiO2 was smaller (2.70 eV) than Mn0.5Zn0.5Fe2O4 (3.04 eV) due to smaller lattice dislocation and microstrain that affect their electronic structure. The Mn0.5Zn0.5Fe2O4/SiO2 showed high photodegradation ability due to smaller optical gap energy and the appearance of SiO2 ligand that can easily attract dye molecules. The Mn0.5Zn0.5Fe2O4/SiO2 also showed high degradation activity even without UV light radiation. The result showed that photodegradation reaction doesn’t follow pseudo-first order kinetics.

Formation of closo-rhodacarboranes with the η2,η3-(CH2=CHC5H6) ligand in the reaction of μ-dichloro-bis[(η4-norbornadiene)rhodium] with nido-dicarbaundecaborates [K][nido-7-R1-8-R2-7,8-C2B9H10

International Nuclear Information System (INIS)

Safronov, A.V.; Sokolova, M.N.; Vorontsov, E.V.; Petrovskij, P.V.; Barakovskaya, I.G.; Chizhevskij, I.T.

2004-01-01

New closo-(η 2 ,η 3 -(4-vinylcyclopentene-3-yl)rhodacarboranes were prepared by reaction of the complex [(η 4 -C 7 H 8 )RhCl] 2 (C 7 H 8 -norbornadiene) with salts of substituted nido-dicarbaundecaborates [K][nido-7-R 1 -8-R 2 -7,8-C 2 B 9 H 10 ] (R 1 =R 2 =H (a); R = R 2 =Me (b); R 1 , R 2 =1',2'-(CH 2 ) 2 C 6 H 4 (c); R 1 =Me, R 2 =Ph (d) in CH 2 Cl 2 . The structure of the compounds prepared in solution was studied by the method of multinuclear NMR spectroscopy. A probable mechanism of the norbornadiene ligand regrouping was suggested [ru

Facile sonochemical synthesis of Zn2SnO4-V2O5 nanocomposite as an effective photocatalyst for degradation of Eosin Yellow.

Science.gov (United States)

Ramasamy Raja, V; Rosaline, D Rani; Suganthi, A; Rajarajan, M

2018-06-01

This study presents a novel method for the preparation of Zn 2 SnO 4 /V 2 O 5 nanocomposites via a sonochemical aqueous route. This method is mild, convenient, cheap and efficient. The as prepared samples were characterized by XRD, SEM, EDAX, TEM, BET, FT-IR and UV-DRS spectra. DRS spectrum shows the adsorption edge of Zn 2 SnO 4 -V 2 O 5 in visible region of spectrum. The structural and morphological features of the as synthesized Zn 2 SnO 4 -V 2 O 5 nanocomposites have been observed using both scanning and transmission electron microscopy. BET surface area analysis inferred that the prepared hetero-junctions are meso-porous in nature. The photocatalytic activity of Zn 2 SnO 4 -V 2 O 5 nanocomposites for the degradation of Eosin Yellow (EY) dye under visible light was investigated in detail. 3% Zn 2 SnO 4 -V 2 O 5 nanocomposite exhibited the highest photocatalytic performance (92% of EY degradation) when compared with 2% Zn 2 SnO 4 -V 2 O 5 and 5% Zn 2 SnO 4 -V 2 O 5 . The adsorption of Eosin Yellow followed the pseudo-first order kinetic model. Simultaneously, high stability of the sample was also investigated by four successive photodegradation of EY under visible light. The relationship between photocatalytic activity and the structure of 3% Zn 2 SnO 4 -V 2 O 5 nanocomposite is discussed, and possible reaction mechanisms are also proposed. Therefore, the facile sonochemical preparation process provides some insight into the application of Zn 2 SnO 4 -V 2 O 5 nanocomposites in photocatalytic degradation of organic pollutants. Copyright © 2018. Published by Elsevier B.V.

Antiferromagnetic ordering in GdRhIn{sub 5}

Energy Technology Data Exchange (ETDEWEB)

Latka, K.; Rams, M. [Marian Smoluchowski Inst. of Physics, Jagiellonian Univ., Krakow (Poland); Kmiec, R.; Pacyna, A.W. [Henryk Niewodniczanski Inst. of Nuclear Physics, Polish Academy of Sciences, Krakow (Poland); Zaremba, V.I. [Inorganic Chemistry Dept., Ivan Franko National Univ. of Lviv, Lviv (Ukraine); Inst. fuer Anorganische und Analytische Chemie, Westfaelische Wilhelms-Univ. Muenster (Germany); Poettgen, R. [Inst. fuer Anorganische und Analytische Chemie, Westfaelische Wilhelms-Univ. Muenster (Germany)

2004-09-01

A polycrystalline sample of tetragonal GdRhIn{sub 5} (HoCoGa{sub 5} type, space group P4/mmm) was obtained by induction melting of the elements in a glassy carbon crucible in a water-cooled sample chamber and subsequent annealing at 670 K. X-ray powder data yielded the cell parameters a = 460.65(7), c = 743.52(12) pm. The magnetic and electronic properties of GdRhIn{sub 5} have been studied by magnetic susceptibility, electrical resistivity, and {sup 155}Gd Moessbauer spectroscopic measurements. Antiferromagnetic ordering is detected at 41.0(2) K. The results are discussed using a simple molecular field approximation. (orig.)

Hydroformylation of 1-Hexene over Rh/Nano-Oxide Catalysts

Directory of Open Access Journals (Sweden)

Sari Suvanto

2013-03-01

Full Text Available The effect of nanostructured supports on the activity of Rh catalysts was studied by comparing the catalytic performance of nano- and bulk-oxide supported Rh/ZnO, Rh/SiO2 and Rh/TiO2 systems in 1-hexene hydroformylation. The highest activity with 100% total conversion and 96% yield of aldehydes was obtained with the Rh/nano-ZnO catalyst. The Rh/nano-ZnO catalyst was found to be more stable and active than the corresponding rhodium catalyst supported on bulk ZnO. The favorable morphology of Rh/nano-ZnO particles led to an increased metal content and an increased number of weak acid sites compared to the bulk ZnO supported catalysts. Both these factors favored the improved catalytic performance. Improvements of catalytic properties were obtained also with the nano-SiO2 and nano-TiO2 supports in comparison with the bulk supports. All of the catalysts were characterized by scanning electron microscope (SEM, inductively coupled plasma mass spectrometry (ICP-MS, BET, powder X-ray diffraction (PXRD and NH3- temperature-programmed desorption (TPD.

Ecologische risico's van koper en zink in het oppervlaktewater

NARCIS (Netherlands)

Bonten, L.T.C.; Vink, J.; Verschoor, A.

2011-01-01

Het merendeel van de Nederlandse (rijks)wateren voldoet niet aan de door de Kaderrichtlijn Water vereiste chemische en ecologische toestand. In veel oppervlaktewateren in Nederland zijn de concentraties van de metalen koper en zink hoger dan de wettelijke normen. Tot dusver is het echter niet

Highly Pathogenic Avian Influenza H5N8 Clade 2.3.4.4b in Germany in 2016/2017

Directory of Open Access Journals (Sweden)

Anja Globig

2018-01-01

Full Text Available Here, we report on the occurrence of highly pathogenic avian influenza (HPAI H5Nx clade 2.3.4.4b in Germany. Between November 8, 2016, and September 30, 2017, more than 1,150 cases of HPAI H5Nx clade 2.3.4.4b in wild birds and 107 outbreaks in birds kept in captivity (92 poultry holdings and 15 zoos/animal parks were reported in Germany. This HPAI epidemic is the most severe recorded in Germany so far. The viruses were apparently introduced by migratory birds, sparking an epidemic among wild birds across Germany with occasional incursions into poultry holdings, zoos and animal parks, which were usually rapidly detected and controlled by stamping out. HPAI viruses (mainly subtype H5N8, in a few cases also H5N5 were found in dead wild birds of at least 53 species. The affected wild birds were water birds (including gulls, storks, herons, and cormorants and scavenging birds (birds of prey, owls, and crows. In a number of cases, substantial gaps in farm biosecurity may have eased virus entry into the holdings. In a second wave of the epidemic starting from February 2017, there was epidemiological and molecular evidence for virus transmission of the infections between commercial turkey holdings in an area of high poultry density, which caused approximately 25% of the total number of outbreaks in poultry. Biosecurity measures in poultry holdings should be adapted. This includes, inter alia, wearing of stable-specific protective clothing and footwear, cleaning, and disinfection of equipment that has been in contact with birds and prevention of contacts between poultry and wild water birds.

Magnetic ordering of Gd/sub x/Er/sub 1-x/Rh4B4 near the superconducting region

International Nuclear Information System (INIS)

Kohn, S.; Wang, R.H.; Smith, J.L.; Huang, C.Y.

1979-01-01

Gd/sub x/Er/sub 1-x/Rh 4 B 4 exhibits superconductivity at some critical temperature T/sub c/ followed by the onset of long-range ferromagnetic ordering at a lower temperature and a loss of superconductivity for x 2 Oe), the extrema in chi (T) and R(T) are depressed and smeared considerably with a corresponding shift in the temperature at which the extrema occur. (2) The sample is not superconducting down to 0.6 K. (3) In the presence of a dc magnetic field, a second ac chi peak appears at a slightly higher temperature. (4) The field dependence of the ac susceptibility resembles that of a spin glass. Details of the field dependence of these observations and the nature of these phenomena will be presented

The John Zink Hamworthy combustion handbook

CERN Document Server

Baukal, Charles E

2013-01-01

Despite the length of time it has been around, its importance, and vast amounts of research, combustion is still far from being completely understood. Issues regarding the environment, cost, and fuel consumption add further complexity, particularly in the process and power generation industries. Dedicated to advancing the art and science of industrial combustion, The John Zink Hamworthy Combustion Handbook, Second Edition: Volume 3 - Applications offers comprehensive, up-to-date coverage of equipment used in the process and power generation industries. Under the leadership of Charles E. Baukal

Hydrothermal synthesis of 4ZnO·B2O3·H2O:Ln3 + (Ln = Eu, Tb) phosphors: Morphology-tunable and luminescence properties

Science.gov (United States)

Cao, Shiwei; Jiao, Yang; Han, Weifang; Ge, Chunhua; Song, Bo; Wang, Jie; Zhang, Xiangdong

2018-02-01

4ZnO·B2O3·H2O:Ln3 + (Ln = Eu, Tb) phosphors with different morphologies have been successfully synthesized via one-step hydrothermal method through regulating the molar amount of Eu3 + and Tb3 +. Comprehensive scanning electron microscopy (SEM), X-ray diffraction (XRD) Fourier transform infrared spectrum (FT-IR) and inductively coupled plasma atomic emission spectrometer (ICP-AES) characterizations all confirm that obtained products are 4ZnO·B2O3·H2O:Ln3 + (Ln = Eu, Tb). The experimental results displayed that the morphology and photoluminescence of compounds is regularly changed with increased the molar amount of rare earth ions. For the Eu3 +-doped, Tb3 +-doped and Eu3 +/Tb3 + co-doped 4ZnO·B2O3·H2O phosphors of morphologies, the rod-like structures gradually changed to flower-like structures, fine wire-like structure and hybrid structure, respectively. To their photoluminescence, the Eu3 + shows a red emission (615 nm); the Tb3 + shows a green emission (545 nm); for the Eu3 +/Tb3 + co-doped 4ZnO·B2O3·H2O phosphors, a combination of blue (5d-4f of Eu2 +), green (5D4-7F5 of Tb3 +) and red (5D0-7F2 of Eu3 +) emissions emerges to achieve white emission. In addition, the energy transfer among Eu3 +, Eu2 + and Tb3 + ions was also discussed.

Hubungan Asupan Asam Folat, Zink, dan Vitamin A Ibu Hamil Trimester III terhadap Berat Badan Lahir di Kabupaten Padang Pariaman

Directory of Open Access Journals (Sweden)

Wici Septiyeni

2016-01-01

Full Text Available Abstrak             Berat badan lahir merupakan salah satu indikator kesehatan bayi baru lahir. Berat badan lahir dipengaruhi oleh berbagai faktor yang salah satunya adalah mikronutrien seperti: asam folat, zink dan vitamin A yang disinyalir memiliki hubungan dengan berat badan lahir.Tujuan penelitian ini adalah menentukan hubungan antara asupan asam folat, seng, dan vitamin A terhadap berat badan lahir. Penelitian ini merupakan cross sectional study pada 59 ibu hamil di Kabupaten Padang Pariaman. Pengumpulan data dilakukan dengan wawancara dan pengukuran berat badan lahir. Analisis statistik yang digunakan adalah uji korelasi Spearman. Hasil penelitian ini yaitu rata-rata umur ibu hamil sebesar 26,5424 tahun. Rata-rata berat badan lahir 3181,36 gram dan rata-rata tinggi badan ibu adalah 153,8305 cm. Rata-rata konsumsi asam folat subjek penelitian adalah 341,9525 ug, zink  5,0727 mg dan vitamin A 688,9300 RE. Hasil analisis menunjukkan tidak terdapat hubungan yang bermakna antara asupan asam folat dan berat badan lahir (p>0,05,asupan zink dan berat badan (p>0,05 dan asupan vitamin A dan berat badan lahir (p>0,05.bKesimpulan penelitian ini adalah bahwa tidak ada hubungan antara asupan asam folat, zink dan vitamin A ibu hamil trimester III terhadap berat badan lahir.Kata kunci: asam folat, zink, vitamin A, berat badan lahir, Ibu hamil trimester III AbstractBirth weight is an indicator of the health of the newborn. Birth weight is influenced by various factors like micronutrients such as: folic acid, zinc and vitamin A which allegedly had a relationship with birth weight. The objective of this study was to determine the relationship between the intake of folic acid, zinc, and vitamin A on birth weight. This study was a cross sectional study to 59 pregnant women in the district of Padang Pariaman. Data collection with interviews and birth weight measurements. Statistical analysis used the Spearman correlation test. The results of this

Interpretation of specific-heat and spontaneous-magnetization anomalies at the reentrant superconducting - ferromagnetic transition in (Ho0.6Er0.4)Rh4B4

International Nuclear Information System (INIS)

Woolf, L.D.; Johnston, D.C.; Mook, H.A.; Koehler, W.C.; Maple, M.B.; Fisk, Z.

1981-09-01

Analysis of neutron-diffraction data on the compound (Ho 0 . 6 Er 0 . 4 )Rh 4 B 4 indicates that the Curie temperature is depressed by about 0.2 K due to the occurrence of superconductivity, in agreement with theoretical predictions. The temperature dependence of the specific heat in the vicinity of the first-order reentrant superconducting - ferromagnetic transition was computed by means of a simple model from the temperature dependence of the spontaneous magnetization of the Ho ions and was found to be in good agreement with the experimental data

Nanocasting of mesoporous LiNi{sub 0.5}Mn{sub 1.5}O{sub 4-δ}. Synthesis, formation mechanism and impact of the host material; Mesoporoeses LiNi{sub 0.5}Mn{sub 1.5}O{sub 4-δ} durch Nanocasting. Darstellung, Bildungsmechanismus und Einfluss der Strukturmatrix

Energy Technology Data Exchange (ETDEWEB)

Vijn, Annalena

2015-11-27

LiNi{sub 0.5}Mn{sub 1.5}O{sub 4-δ} is one of the most attractive active materials for cathodes for lithium ion batteries. As shown before the electrochemical performance of an active material can be enhanced by employing nanostructuring. The objective of this study was to synthesize mesoporous LiNi{sub 0.5}Mn{sub 1.5}O{sub 4-δ} via hard-template materials and to investigate the impact of the confined pore space on the formation of LiNi{sub 0.5}Mn{sub 1.5}O{sub 4-δ}, as well as the impact of the template material (silica and carbon). [German] LiNi{sub 0.5}Mn{sub 1.5}O{sub 4-δ} stellt eines der vielversprechendsten Aktivmaterialien fuer die Kathoden von Lithium-Ionen-Batterien dar. Wie bereits gezeigt wurde, kann die Nanostrukturierung des Aktivmaterials einer Elektrode zu einer Verbesserung der elektrochemischen Eigenschaften fuehren. Ziel dieser Arbeit war es, mesoporoeses LiNi{sub 0.5}Mn{sub 1.5}O{sub 4-δ} darzustellen und den Einfluss des beengten Raumes der Mesoporen und der Templatmaterialien Silica und Kohlenstoff auf die Bildung von LiNi{sub 0.5}Mn{sub 1.5}O{sub 4-δ} zu untersuchen.

Spectroscopic ellipsometry study of Cu2ZnSnSe4 bulk crystals

International Nuclear Information System (INIS)

León, M.; Lopez, N.; Merino, J. M.; Caballero, R.; Levcenko, S.; Gurieva, G.; Serna, R.; Bodnar, I. V.; Nateprov, A.; Guc, M.; Arushanov, E.; Schorr, S.; Perez-Rodriguez, A.

2014-01-01

Using spectroscopic ellipsometry we investigated and analyzed the pseudo-optical constants of Cu 2 ZnSnSe 4 bulk crystals, grown by the Bridgman method, over 0.8–4.5 eV photon energy range. The structures found in the spectra of the complex pseudodielectric functions were associated to E 0 , E 1A , and E 1B interband transitions and were analyzed in frame of the Adachi's model. The interband transition parameters such as strength, threshold energy, and broadening were evaluated by using the simulated annealing algorithm. In addition, the pseudo-complex refractive index, extinction coefficient, absorption coefficient, and normal-incidence reflectivity were derived over 0.8–4.5 eV photon energy range

Facile synthesis of carbon-ZnO nanocomposite with enhanced visible light photocatalytic performance

Energy Technology Data Exchange (ETDEWEB)

Akir, Sana [Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, UMR 8520 − IEMN, F-59000, Centrale Lille (France); Laboratoire de Physique des Matériaux Lamellaires et Nano-Matériaux Hybrides, Faculté des Sciences de Bizerte, Université de Carthage, 7021, Bizerte (Tunisia); Laboratoire de Physico-chimie des Matériaux Minéraux et leurs Applications, Centre National des Recherches en Sciences des Matériaux, Technopôle de Bordj Cedria, BP73, 8027, Soliman (Tunisia); Hamdi, Abderrahmane [Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, UMR 8520 − IEMN, F-59000, Centrale Lille (France); Laboratoire de Physique des Matériaux Lamellaires et Nano-Matériaux Hybrides, Faculté des Sciences de Bizerte, Université de Carthage, 7021, Bizerte (Tunisia); Laboratory of Semi-conductors, Nano-structures and Advanced Technologies, Research and Technology Centre of Energy, Borj-Cedria Science and Technology Park, BP 95, 2050, Hammam-Lif (Tunisia); Addad, Ahmed [UMET, UMR CNRS 8207, Université Lille 1, 59655 Villeneuve d' Ascq Cédex (France); Coffinier, Yannick [Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, UMR 8520 − IEMN, F-59000, Centrale Lille (France); Boukherroub, Rabah, E-mail: rabah.boukherroub@iemn.univ-lille1.fr [Univ. Lille, CNRS, Centrale Lille, ISEN, Univ. Valenciennes, UMR 8520 − IEMN, F-59000, Centrale Lille (France); and others

2017-04-01

Highlights: • C-ZnO nanocomposite was successfully prepared via a facile and eco-friendly process. • C-ZnO NPs have excellent photocatalytic activity for RhB dye degradation under visible light irradiation compared with literature. • The visible photocatalytic properties originate from injection e{sup −} in CB of ZnO from RhB. - Abstract: The present study describes a facile route for synthesis of carbon-ZnO nanocomposites (C-ZnO) via hydrothermal process in presence of glucose as carbon precursor. The samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), UV–vis diffuse reflectance spectroscopy (DRS) and photoluminescence (PL) measurements. The results showed carbon uniformly coated on the surface of the ZnO nanoparticles to form the C-ZnO nanocomposites. Further investigation revealed that carbon could significantly protect ZnO NPs against the coalescence during high temperature treatment. The obtained C-ZnO nanocomposite showed excellent photocatalytic activity for the degradation of rhodamine B (RhB) under visible light irradiation, which was attributed to the repressed charge carrier recombination in the nanocomposite. Quenching experiments and photocurrent measurements revealed a photocatalytic mechanism occurring through photosensitization.

Zinc oxide for spintronic applications. Sol-gel processes and characterization; Zinkoxid fuer spintronische Anwendungen. Sol-Gel-Prozesse und Charakterisierung

Energy Technology Data Exchange (ETDEWEB)

Knies, Christoph

2009-06-15

results of these measurements seem however to underly a statistical distribution and let no correlation with the specific doping of each sample to be recognized. In order to study the influence of the doping on the charge carriers magnetotransport experiments were performed. Again and correspondingly to the results of the MCD and ESR studies no hints on a ferromagnetic order could be found. Instead the behaviour observed in the experiments can be explained by the formation of a common disturbance band of flat donor and Co level. [German] Seit dem Jahr 1999 veroeffentlichte theoretische Modelle sagen fuer Systeme auf Basis von Cobalt-dotiertem Zinkoxid die Bildung einer ferromagnetischen Ordnung mit Curie-Temperaturen oberhalb der Raumtemperatur voraus. Wesentliche Bedingung fuer das Auftreten der ferromagnetischen Wechselwirkung ist das Vorhandensein von zusaetzlichen Ladungstraegern, die mit den d-Zustaenden des Cobalts wechselwirken. Das Ziel dieser Arbeit stellt die Herstellung von Cobalt-dotierten Zinkoxid-Duennschichten mit Hilfe des Tauchbeschichtungsverfahrens, die Charakterisierung der Eigenschaften des Materials sowie die Untersuchung der durch zusaetzliche Dotierung mit flachen Donatoren entstehenden Effekte auf die magnetischen Eigenschaften und den Ladungstraegertransport dar. Die strukturellen Charakterisierung mittels Roentgendiffraktometrie weist auf ein einphasiges nanokristallines Wachstum des ZnO in Wurtzitstruktur bei einer mittleren Teilchengroesse zwischen 20 und 30 nm hin. Cobalt-basierte Fremdphasen koennen fuer Dotierkonzentrationen oberhalb von 20 % beobachtet werden. Optische und Magnetresonanz-Untersuchungen lassen keinen Zweifel am Einbau des Co im 2+ Ladungszustand auf dem Gitterplatz des Zinks in 3d{sup 7} Konfiguration. In Messungen der optischen Absorption und des magnetischen Zirkulardichroismus (MCD) sind die internen Kristallfelduebergaenge des Co{sup 2+} im sichtbaren und zusaetzlich im nahen infraroten Spektralbereich zu beobachten

RH-TRU Waste Content Codes (RH TRUCON)

International Nuclear Information System (INIS)

2007-01-01

The Remote-Handled Transuranic (RH-TRU) Content Codes (RH-TRUCON) document describes the inventory of RH-TRU waste within the transportation parameters specified by the Remote-Handled Transuranic Waste Authorized Methods for Payload Control (RH-TRAMPAC).1 The RH-TRAMPAC defines the allowable payload for the RH-TRU 72-B. This document is a catalog of RH-TRU 72-B authorized contents by site. A content code is defined by the following components: (1) A two-letter site abbreviation that designates the physical location of the generated/stored waste (e.g., ID for Idaho National Laboratory [INL]). The site-specific letter designations for each of the sites are provided in Table 1. (2) A three-digit code that designates the physical and chemical form of the waste (e.g., content code 317 denotes TRU Metal Waste). For RH-TRU waste to be transported in the RH-TRU 72-B, the first number of this three-digit code is ''3''. The second and third numbers of the three-digit code describe the physical and chemical form of the waste. Table 2 provides a brief description of each generic code. Content codes are further defined as subcodes by an alpha trailer after the three-digit code to allow segregation of wastes that differ in one or more parameter(s). For example, the alpha trailers of the subcodes ID 322A and ID 322B may be used to differentiate between waste packaging configurations. As detailed in the RH-TRAMPAC, compliance with flammable gas limits may be demonstrated through the evaluation of compliance with either a decay heat limit or flammable gas generation rate (FGGR) limit per container specified in approved content codes. As applicable, if a container meets the watt*year criteria specified by the RH-TRAMPAC, the decay heat limits based on the dose-dependent G value may be used as specified in an approved content code. If a site implements the administrative controls outlined in the RH-TRAMPAC and Appendix 2.4 of the RH-TRU Payload Appendices, the decay heat or FGGR

RH-TRU Waste Content Codes (RH TRUCON)

Energy Technology Data Exchange (ETDEWEB)

Washington TRU Solutions

2007-05-01

The Remote-Handled Transuranic (RH-TRU) Content Codes (RH-TRUCON) document describes the inventory of RH-TRU waste within the transportation parameters specified by the Remote-Handled Transuranic Waste Authorized Methods for Payload Control (RH-TRAMPAC).1 The RH-TRAMPAC defines the allowable payload for the RH-TRU 72-B. This document is a catalog of RH-TRU 72-B authorized contents by site. A content code is defined by the following components: • A two-letter site abbreviation that designates the physical location of the generated/stored waste (e.g., ID for Idaho National Laboratory [INL]). The site-specific letter designations for each of the sites are provided in Table 1. • A three-digit code that designates the physical and chemical form of the waste (e.g., content code 317 denotes TRU Metal Waste). For RH-TRU waste to be transported in the RH-TRU 72-B, the first number of this three-digit code is “3.” The second and third numbers of the three-digit code describe the physical and chemical form of the waste. Table 2 provides a brief description of each generic code. Content codes are further defined as subcodes by an alpha trailer after the three-digit code to allow segregation of wastes that differ in one or more parameter(s). For example, the alpha trailers of the subcodes ID 322A and ID 322B may be used to differentiate between waste packaging configurations. As detailed in the RH-TRAMPAC, compliance with flammable gas limits may be demonstrated through the evaluation of compliance with either a decay heat limit or flammable gas generation rate (FGGR) limit per container specified in approved content codes. As applicable, if a container meets the watt*year criteria specified by the RH-TRAMPAC, the decay heat limits based on the dose-dependent G value may be used as specified in an approved content code. If a site implements the administrative controls outlined in the RH-TRAMPAC and Appendix 2.4 of the RH-TRU Payload Appendices, the decay heat or FGGR

Effects of recombinant human interleukin-8 (rhIL-8) on the bone marrow cells of normal BALB/c mice

International Nuclear Information System (INIS)

Liu Yulong; Zhou Jianying; Wang Guoquan; Dai Hong; Duan Yingying; Guo Xiaokui

2001-01-01

Objective: To observe the colony formation ability of recombinant human interleukin-8 (rhIL-8) on bone marrow cells (BMCs) of normal mice in vivo. Methods: By means of cells culture and flow cytometry (FCM), the colony-stimulating activity of rhIL-8 on BMCs of normal mice was studied. Results: The experimental studies in vivo demonstrated that rhIL-8 could not changed the counts of CFU-GM and distribution of cell cycle in BMCs. Conclusion: rhIL-8 has no colony-stimulating activity to BMCs of normal mice

Deutsch-slawischer Siedlungs- und Sprachkontakt im Gebiet zwischen Saale und Neiße – vorgestellt an ausgewählten Ortsnamen (Siedlungsnamen

Directory of Open Access Journals (Sweden)

Inge Bily

2015-12-01

Full Text Available Saale und Elbe bilden im Wesentlichen die westliche Begrenzung des ehemals kompakten altsorbischen Sprachgebietes. Im Norden schließt das Altsorbische an das Altpolabische, im Osten und Südosten an das Polnische und Tschechische an. Eigennamen bilden eine wichtige Quelle sowohl für die Aufhellung der Geschichte der Besiedlung wie auch ethnischer, sprachlicher und sozialer Verhältnisse, denn historische Siedlungsprozesse fanden ihren Niederschlag u.a. in historischen Belegen von Namen. Diese Belege wie auch die Ableitungsbasen und Benennungsmotive ebenso wie die phonologischen und morphologischen Merkmale der Namen des altsorbischen Kontaktgebietes enthalten eine Vielzahl von Zeugnissen deutsch-slawischer Kontinuität. Auf der Grundlage umfangreicher Studien zu Ortsnamen stellt der Beitrag ausgewählte Beispiele vor. Im ehemals altsorbischen Kontaktgebiet können Ortsnamen (Siedlungsnamen und ihre historische Überlieferung Hinweise auf Siedlungs- und Sprachkontakt geben. Dies belegen eine ganze Reihe von Merkmalen, so z.B.: 1. Unterscheidende Bestimmungswörter 2. Parallele Namengebung mit zeitweiliger Mehrnamigkeit 3. Umbenennung 4. Übersetzung 5. Benennungsparallelismus im deutsch-slawischen Kontaktgebiet 6. Scheinbare sekundäre semantische Verankerung (SSSV 7. Namenpaare 8. Unterscheidende Zusätze 9. Mischnamen (Hybride

Synthesis of nanocrystalline nickel-zinc ferrite (Ni0.8Zn0.2Fe2O4) thin films by chemical bath deposition method

International Nuclear Information System (INIS)

Pawar, D.K.; Pawar, S.M.; Patil, P.S.; Kolekar, S.S.

2011-01-01

Graphical abstract: Display Omitted Research highlights: → We have successfully synthesized nickel-zinc ferrite (Ni 0.8 Zn 0.2 Fe 2 O 4 ) thin films on stainless steel substrates using a low temperature chemical bath deposition method. → The surface morphological study showed the compact flakes like morphology. → The as-deposited thin films are hydrophilic (10 o o ) whereas the annealed thin films are super hydrophilic (θ o ) in nature. → Ni 0.8 Zn 0.2 Fe 2 O 4 thin films could be used in supercapacitor. - Abstract: The nickel-zinc ferrite (Ni 0.8 Zn 0.2 Fe 2 O 4 ) thin films have been successfully deposited on stainless steel substrates using a chemical bath deposition method from alkaline bath. The films were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), static water contact angle and cyclic voltammetry measurements. The X-ray diffraction pattern shows that deposited Ni 0.8 Zn 0.2 Fe 2 O 4 thin films were oriented along (3 1 1) plane. The FTIR spectra showed strong absorption peaks around 600 cm -1 which are typical for cubic spinel crystal structure. SEM study revealed compact flakes like morphology having thickness ∼1.8 μm after air annealing. The annealed films were super hydrophilic in nature having a static water contact angle (θ) of 5 o .The electrochemical supercapacitor study of Ni 0.8 Zn 0.2 Fe 2 O 4 thin films has been carried out in 6 M KOH electrolyte. The values of interfacial and specific capacitances obtained were 0.0285 F cm -2 and 19 F g -1 , respectively.

RH-TRU Waste Content Codes (RH-Trucon)

International Nuclear Information System (INIS)

2007-01-01

The Remote-Handled Transuranic (RH-TRU) Content Codes (RH-TRUCON) document describes the inventory of RH-TRU waste within the transportation parameters specified by the Remote-Handled Transuranic Waste Authorized Methods for Payload Control (RH-TRAMPAC).1 The RH-TRAMPAC defines the allowable payload for the RH-TRU 72-B. This document is a catalog of RH-TRU 72-B authorized contents by site. A content code is defined by the following components: A two-letter site abbreviation that designates the physical location of the generated/stored waste (e.g., ID for Idaho National Laboratory [INL]). The site-specific letter designations for each of the sites are provided in Table 1. A three-digit code that designates the physical and chemical form of the waste (e.g., content code 317 denotes TRU Metal Waste). For RH-TRU waste to be transported in the RH-TRU 72-B, the first number of this three-digit code is '3.' The second and third numbers of the three-digit code describe the physical and chemical form of the waste. Table 2 provides a brief description of each generic code. Content codes are further defined as subcodes by an alpha trailer after the three-digit code to allow segregation of wastes that differ in one or more parameter(s). For example, the alpha trailers of the subcodes ID 322A and ID 322B may be used to differentiate between waste packaging configurations. As detailed in the RH-TRAMPAC, compliance with flammable gas limits may be demonstrated through the evaluation of compliance with either a decay heat limit or flammable gas generation rate (FGGR) limit per container specified in approved content codes. As applicable, if a container meets the watt*year criteria specified by the RH-TRAMPAC, the decay heat limits based on the dose-dependent G value may be used as specified in an approved content code. If a site implements the administrative controls outlined in the RH-TRAMPAC and Appendix 2.4 of the RH-TRU Payload Appendices, the decay heat or FGGR limits based

RH-TRU Waste Content Codes (RH-TRUCON)

International Nuclear Information System (INIS)

2007-01-01

The Remote-Handled Transuranic (RH-TRU) Content Codes (RH-TRUCON) document describes the inventory of RH-TRU waste within the transportation parameters specified by the Remote-Handled Transuranic Waste Authorized Methods for Payload Control (RH-TRAMPAC).1 The RH-TRAMPAC defines the allowable payload for the RH-TRU 72-B. This document is a catalog of RH-TRU 72-B authorized contents by site. A content code is defined by the following components: A two-letter site abbreviation that designates the physical location of the generated/stored waste (e.g., ID for Idaho National Laboratory [INL]). The site-specific letter designations for each of the sites are provided in Table 1. A three-digit code that designates the physical and chemical form of the waste (e.g., content code 317 denotes TRU Metal Waste). For RH-TRU waste to be transported in the RH-TRU 72-B, the first number of this three-digit code is '3.' The second and third numbers of the three-digit code describe the physical and chemical form of the waste. Table 2 provides a brief description of each generic code. Content codes are further defined as subcodes by an alpha trailer after the three-digit code to allow segregation of wastes that differ in one or more parameter(s). For example, the alpha trailers of the subcodes ID 322A and ID 322B may be used to differentiate between waste packaging configurations. As detailed in the RH-TRAMPAC, compliance with flammable gas limits may be demonstrated through the evaluation of compliance with either a decay heat limit or flammable gas generation rate (FGGR) limit per container specified in approved content codes. As applicable, if a container meets the watt*year criteria specified by the RH-TRAMPAC, the decay heat limits based on the dose-dependent G value may be used as specified in an approved content code. If a site implements the administrative controls outlined in the RH-TRAMPAC and Appendix 2.4 of the RH-TRU Payload Appendices, the decay heat or FGGR limits based

RH-TRU Waste Content Codes (RH-TRUCON)

Energy Technology Data Exchange (ETDEWEB)

Washington TRU Solutions LLC

2007-08-01

The Remote-Handled Transuranic (RH-TRU) Content Codes (RH-TRUCON) document describes the inventory of RH-TRU waste within the transportation parameters specified by the Remote-Handled Transuranic Waste Authorized Methods for Payload Control (RH-TRAMPAC).1 The RH-TRAMPAC defines the allowable payload for the RH-TRU 72-B. This document is a catalog of RH-TRU 72-B authorized contents by site. A content code is defined by the following components: • A two-letter site abbreviation that designates the physical location of the generated/stored waste (e.g., ID for Idaho National Laboratory [INL]). The site-specific letter designations for each of the sites are provided in Table 1. • A three-digit code that designates the physical and chemical form of the waste (e.g., content code 317 denotes TRU Metal Waste). For RH-TRU waste to be transported in the RH-TRU 72-B, the first number of this three-digit code is “3.” The second and third numbers of the three-digit code describe the physical and chemical form of the waste. Table 2 provides a brief description of each generic code. Content codes are further defined as subcodes by an alpha trailer after the three-digit code to allow segregation of wastes that differ in one or more parameter(s). For example, the alpha trailers of the subcodes ID 322A and ID 322B may be used to differentiate between waste packaging configurations. As detailed in the RH-TRAMPAC, compliance with flammable gas limits may be demonstrated through the evaluation of compliance with either a decay heat limit or flammable gas generation rate (FGGR) limit per container specified in approved content codes. As applicable, if a container meets the watt*year criteria specified by the RH-TRAMPAC, the decay heat limits based on the dose-dependent G value may be used as specified in an approved content code. If a site implements the administrative controls outlined in the RH-TRAMPAC and Appendix 2.4 of the RH-TRU Payload Appendices, the decay heat or FGGR

RH-TRU Waste Content Codes (RH-TRUCON)

Energy Technology Data Exchange (ETDEWEB)

Washington TRU Solutions

2007-05-30

The Remote-Handled Transuranic (RH-TRU) Content Codes (RH-TRUCON) document describes the inventory of RH-TRU waste within the transportation parameters specified by the Remote-Handled Transuranic Waste Authorized Methods for Payload Control (RH-TRAMPAC).1 The RH-TRAMPAC defines the allowable payload for the RH-TRU 72-B. This document is a catalog of RH-TRU 72-B authorized contents by site. A content code is defined by the following components: • A two-letter site abbreviation that designates the physical location of the generated/stored waste (e.g., ID for Idaho National Laboratory [INL]). The site-specific letter designations for each of the sites are provided in Table 1. • A three-digit code that designates the physical and chemical form of the waste (e.g., content code 317 denotes TRU Metal Waste). For RH-TRU waste to be transported in the RH-TRU 72-B, the first number of this three-digit code is “3.” The second and third numbers of the three-digit code describe the physical and chemical form of the waste. Table 2 provides a brief description of each generic code. Content codes are further defined as subcodes by an alpha trailer after the three-digit code to allow segregation of wastes that differ in one or more parameter(s). For example, the alpha trailers of the subcodes ID 322A and ID 322B may be used to differentiate between waste packaging configurations. As detailed in the RH-TRAMPAC, compliance with flammable gas limits may be demonstrated through the evaluation of compliance with either a decay heat limit or flammable gas generation rate (FGGR) limit per container specified in approved content codes. As applicable, if a container meets the watt*year criteria specified by the RH-TRAMPAC, the decay heat limits based on the dose-dependent G value may be used as specified in an approved content code. If a site implements the administrative controls outlined in the RH-TRAMPAC and Appendix 2.4 of the RH-TRU Payload Appendices, the decay heat or FGGR

Polymorphic one-dimensional (N2H4)2ZnTe: soluble precursors for the formation of hexagonal or cubic zinc telluride.

Science.gov (United States)

Mitzi, David B

2005-10-03

Two hydrazine zinc(II) telluride polymorphs, (N2H4)2ZnTe, have been isolated, using ambient-temperature solution-based techniques, and the crystal structures determined: alpha-(N2H4)2ZnTe (1) [P21, a = 7.2157(4) Angstroms, b = 11.5439(6) Angstroms, c = 7.3909(4) Angstroms, beta = 101.296(1) degrees, Z = 4] and beta-(N2H4)2ZnTe (2) [Pn, a = 8.1301(5) Angstroms, b = 6.9580(5) Angstroms, c = 10.7380(7) Angstroms, beta = 91.703(1) degrees, Z = 4]. The zinc atoms in 1 and 2 are tetrahedrally bonded to two terminal hydrazine molecules and two bridging tellurium atoms, leading to the formation of extended one-dimensional (1-D) zinc telluride chains, with different chain conformations and packings distinguishing the two polymorphs. Thermal decomposition of (N2H4)2ZnTe first yields crystalline wurtzite (hexagonal) ZnTe at temperatures as low as 200 degrees C, followed by the more stable zinc blende (cubic) form at temperatures above 350 degrees C. The 1-D polymorphs are soluble in hydrazine and can be used as convenient precursors for the low-temperature solution processing of p-type ZnTe semiconducting films.

Radiation chemical behavior of Rh(III) in HClO4 and HNO3

International Nuclear Information System (INIS)

Vladimirova, M.V.; Khalkina, E.V.

1995-01-01

The radiation chemical behavior of Rh is very interesting since Rh accumulates in irradiated U but has not been reported in the literature. Scattered data do exist for the radiation chemical behavior of Rh(III) in weakly acidic and alkaline solutions. Pulsed radiolysis was used to investigate the formation of unstable oxidation states of Rh during reduction and oxidation of Rh(III) in neutral solutions. The rate constant of the reaction Rh(III) + e aq - was found to be 6·10 10 liter/mole·sec. The radiation chemical behavior of Rh(III) toward γ-radiolysis in neutral, weakly acidic (up to 0.1 N), and alkaline solutions was examined. In neutral solutions of [Rh(NH 3 ) 5 Cl]Cl 2 and RhCl 3 , metallic Rh is formed. The degree of reduction is ∼ 1%. In neutral and weakly acidic solutions of Rh(NO 3 ) 3 , Rh 2 O 3 ·xH 2 O is formed. Irradiation of Rh(ClO 4 ) 3 solutions produces no reduction. The radiation chemical behavior of Rh(III) in HClO 4 and HNO 3 solutions at concentrations > 1 M is studied in the present work

Synthesis, crystal structure and electronic structure of the binary phase Rh{sub 2}Cd{sub 5}

Energy Technology Data Exchange (ETDEWEB)

Koley, Biplab [Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur 721302 (India); Chatterjee, S. [Department of Physics, Indian Institute of Technology Kharagpur, Kharagpur 721302 (India); Jana, Partha P., E-mail: ppj@chem.iitkgp.ernet.in [Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur 721302 (India)

2017-02-15

A new phase in the Rh-Cd binary system - Rh{sub 2}Cd{sub 5} has been identified and characterized by single crystal X-ray diffraction and Energy dispersive X-ray analysis. The stoichiometric compound Rh{sub 2}Cd{sub 5} crystallizes with a unit cell containing 14 atoms, in the orthorhombic space group Pbam (55). The crystal structure of Rh{sub 2}Cd{sub 5} can be described as a defect form of the In{sub 3}Pd{sub 5} structure with ordered vacancies, formed of two 2D atomic layers with the stacking sequence: ABAB. The A type layers consist of (3.6.3.6)-Kagomé nets of Cd atoms while the B type layers consist of (3{sup 5}) (3{sup 7})- nets of both Cd and Rh atoms. The stability of this line phase is investigated by first principle electronic structure calculations on the model of ordered Rh{sub 2}Cd{sub 5}. - Graphical abstract: (3.6.3.6)-Kagomé nets of cadmium atoms (top) and (3{sup 5}) (3{sup 7})- nets of both cadmium and rhodium atoms (bottom) in the structure of Rh{sub 2}Cd{sub 5}.

Comparative studies of the dielectric properties of (1−x)BiFeO{sub 3}-xNi{sub 0.8}Zn{sub 0.2}Fe{sub 2}O{sub 4} (x=0.0, 0.2, 0.5, 0.8, 1.0) multiferroic nanocomposite with their single phase BiFeO{sub 3} and Ni{sub 0.8}Zn{sub 0.2}Fe{sub 2}O{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Mani, Angom Devadatta, E-mail: angomdevadattamani@gmail.com; Soibam, Ibetombi

2017-02-15

BiFeO{sub 3} (BFO) and nickel zinc ferrite Ni{sub 0.8}Zn{sub 0.2}Fe{sub 2}O{sub 4} (NZFO) were prepared by sol gel and auto combustion route respectively. Stoichiometric proportions were mixed to obtain the multiferroic nanocomposites having the compositional formula (1−x)BiFeO{sub 3}-x Ni{sub 0.8}Zn{sub 0.2}Fe{sub 2}O{sub 4} (x=0.0, 0.2, 0.5, 0.8, 1.0). The phases were confirmed by XRD analyses. SEM micrographs showed the agglomerated nature of the particles with continuous grain growth in all directions. Elemental compositions were confirmed from EDAX studies. FTIR studies showed the stretching and bending vibrations of the various bonds present in the samples. The dielectric properties such as dielectric constant, ε′ and dielectric loss tangent, tanδ were studied for the spinel, perovskite and nanocomposite ferrites. Experimental result shows an increasing trend in the value of dielectric constant in going from spinel to perovskite phase. The frequency dependence of tanδ showed minimum loss for x=0.5 nanocomposite. Possible mechanisms explaining the above results were being discussed.

Enhanced photocatalytic activity of ZnS nanoparticles loaded with MoS{sub 2} nanoflakes by self-assembly approach

Energy Technology Data Exchange (ETDEWEB)

Vattikuti, S.V. Prabhakar, E-mail: vsvprabu@gmail.com; Byon, Chan, E-mail: cbyon@ynu.ac.kr; Jeon, Sora

2016-12-01

A hybrid consisting of ZnS nanoparticles supported on layered MoS{sub 2}−ZnS was synthesized by a hydrothermal method based on self-assembly technique without using a template. XRD, SEM-EDX, TEM, HR-TEM, TG-DTA, XPS, N{sub 2} adsorption-desorption, and UV–Vis spectroscopies were used to characterize the structural features, morphology, and composition of the MoS{sub 2}–ZnS hybrid. The results show that the MoS{sub 2}–ZnS hybrid is mainly ZnS nanoparticles on layered MoS{sub 2} with a thickness of ca. 5–20 nm. The combination of the MoS{sub 2} and ZnS hybrid structure is beneficial for enhancing the photocatalytic degradation of rhodamine B (RhB) under visible light irradiation. A possible photoreaction mechanism of the MoS{sub 2}–ZnS hybrid in the degradation is proposed. The photoexcited electrons from the ZnS could easily transfer to the conduction band of MoS{sub 2}, thus decreasing the recombination of photoinduced carriers and enabling the degradation of RhB under visible light irradiation.

Crystal structure, energy transfer and tunable luminescence properties of Ca8ZnCe(PO4)7:Eu2+,Mn2+ phosphor

Science.gov (United States)

Ding, Chong; Tang, Wanjun

2018-02-01

Single-phased Ca8ZnCe(PO4)7:Eu2+,Mn2+ phosphors with whitlockite-type structure have been prepared via the combustion-assisted synthesis technique. The XRD pattern show that the as-obtained phosphors crystallize in a trigonal phase with space group of R-3c (161). Ca8ZnCe(PO4)7 host is full of sensitizers (Ce3+) and the Ce3+ emission at different lattice sites has been discussed. The efficient energy transfers from Ce3+ ions to Eu2+/Mn2+ ions and from Eu2+ to Mn2+ have been validated. Under UV excitation, the emitting color of Ca8ZnCe(PO4)7:Eu2+/Mn2+ samples can be modulated from violet blue to green and from violet blue to red-orange by the energy transfers of Ce3+→Eu2+ and Ce3+→Mn2+, respectively. Additionally, white emission has been obtained through adjusting the relative concentrations of Eu2+ and Mn2+ ions in the Ca8ZnCe(PO4)7 host under UV excitation. These results indicate that as-prepared Ca8ZnCe(PO4)7:Eu2+,Mn2+ may be a potential candidate as color-tunable white light-emitting phosphors.

Organic Dye Degradation Under Solar Irradiation by Hydrothermally Synthesized ZnS Nanospheres

Science.gov (United States)

Samanta, Dhrubajyoti; Chanu, T. Inakhunbi; Basnet, Parita; Chatterjee, Somenath

2018-02-01

The green synthesis of ZnS nanospheres using Citrus limetta (sweet lime) juice as a capping agent through a conventional hydrothermal method was studied. The particle size, morphology, chemical composition, band gap, and optical properties of the synthesized ZnS nanospheres were characterized using x-ray diffraction spectroscopy, field emission scanning electron microscopy, high-resolution transmission electron microscopy, and ultraviolet-visible spectroscopy. The photocatalytic activity of the ZnS nanospheres was evaluated by degradation of rhodamine B (RhB) and methyl orange (MO) under solar irradiation. Upon 150 min of solar irradiation, the extent of degradation was 94% and 77% for RhB and MO, respectively.

WARM SPITZER OBSERVATIONS OF THREE HOT EXOPLANETS: XO-4b, HAT-P-6b, AND HAT-P-8b

Energy Technology Data Exchange (ETDEWEB)

Todorov, Kamen O. [Department of Astronomy and Astrophysics, The Pennsylvania State University, University Park, PA 16802 (United States); Deming, Drake [Planetary Systems Laboratory, NASA' s Goddard Space Flight Center, Greenbelt, MD 20771 (United States); Knutson, Heather A. [Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, CA 91125 (United States); Burrows, Adam [Department of Astrophysical Sciences, Princeton University, Princeton, NJ 05844 (United States); Sada, Pedro V. [Department of Physics and Mathematics, University of Monterrey, Monterrey (Mexico); Cowan, Nicolas B. [Department of Physics and Astronomy, Northwestern University, Evanston, IL 60208 (United States); Agol, Eric [Department of Astronomy, University of Washington, Box 351580, Seattle, WA 98195 (United States); Desert, Jean-Michel; Charbonneau, David [Harvard-Smithsonian Center for Astrophysics, Cambridge, MA 02138 (United States); Fortney, Jonathan J.; Laughlin, Gregory [Department of Astronomy and Astrophysics, University of California at Santa Cruz, Santa Cruz, CA 95064 (United States); Langton, Jonathan [Department of Physics, Principia College, Elsah, IL 62028 (United States); Showman, Adam P.; Lewis, Nikole K. [Lunar and Planetary Laboratory, University of Arizona, Tucson, AZ 85721 (United States)

2012-02-10

We analyze Warm Spitzer/Infrared Array Camera observations of the secondary eclipses of three planets, XO-4b, HAT-P-6b, and HAT-P-8b. We measure secondary eclipse amplitudes at 3.6 {mu}m and 4.5 {mu}m for each target. XO-4b exhibits a stronger eclipse depth at 4.5 {mu}m than at 3.6 {mu}m, which is consistent with the presence of a temperature inversion. HAT-P-8b shows a stronger eclipse amplitude at 3.6 {mu}m and is best described by models without a temperature inversion. The eclipse depths of HAT-P-6b can be fitted with models with a small or no temperature inversion. We consider our results in the context of a postulated relationship between stellar activity and temperature inversion and a relationship between irradiation level and planet dayside temperature, as discussed by Knutson et al. and Cowan and Agol, respectively. Our results are consistent with these hypotheses, but do not significantly strengthen them. To measure accurate secondary eclipse central phases, we require accurate ephemerides. We obtain primary transit observations and supplement them with publicly available observations to update the orbital ephemerides of the three planets. Based on the secondary eclipse timing, we set upper boundaries for ecos ({omega}) for HAT-P-6b, HAT-P-8b, and XO-4b and find that the values are consistent with circular orbits.

Standard enthalpies of formation of selected Rh2YZ Heusler compounds

International Nuclear Information System (INIS)

Yin, Ming; Nash, Philip

2015-01-01

The standard enthalpies of formation (Δ f H°) of selected ternary Rh-based Rh 2 YZ (Y = Cu, Fe, Mn, Ni, Ru, Ti, V; Z = Al, Ga, In, Si, Ge, Sn) compounds were measured using high temperature direct reaction calorimetry. The measured standard enthalpies of formation (in kJ/mol of atoms) are, for the Heusler compound Rh 2 MnSn (−40.1 ± 3.6), for the B2-structured compounds: Rh 2 FeAl (−48.5 ± 2.9); Rh 2 MnAl (−72.4 ± 2.7); Rh 2 MnGa (−55.3 ± 2.0); Rh 2 MnIn (−35.3 ± 1.9), for the tetragonal compounds: Rh 2 FeSn (−28.9 ± 1.3); Rh 2 TiAl (−97.6 ± 2.2); Rh 2 TiGa (−79.0 ± 1.8); Rh 2 TiSn (−74.7 ± 3.1). Values are compared with those from first principles calculations in published papers and the Open Quantum Materials Database (OQMD). Lattice parameters of these compounds are determined using X-ray diffraction analysis (XRD). Microstructures were characterized using scanning electron microscopy (SEM) and Energy Dispersive Spectroscopy (EDS). - Highlights: • Standard enthalpies of formation of Rh 2 YZ were measured using a drop calorimeter. • Measured enthalpies agree with first principles data in general. • Lattice parameters and related phase relationships were consistent with literature data. • Rh 2 TiSn of tI8 structure were reported for the first time.

Solid-State Synthesis and Structure of the Enigmatic Ammonium Octaborate: (NH4)2[B7O9(OH)5]·3/4B(OH)3·5/4H2O.

Science.gov (United States)

Neiner, Doinita; Sevryugina, Yulia V; Schubert, David M

2016-09-06

The compound known since the 19th century as ammonium octaborate was structurally characterized revealing the ammonium salt of the ribbon isomer of the heptaborate anion, [B7O9(OH)5](2-), with boric acid and water molecules. Of composition (NH4)2B7.75O12.63·4.88H2O, it approximates the classical ammonium octaborate composition (NH4)2B8O13·6H2O and has the structural formula {(NH4)2[B7O9(OH)5]}4·3B(OH)3·5H2O. It spontaneously forms at room temperature in solid-state mixtures of ammonium tetraborate and ammonium pentaborate. It crystallizes in the monoclinic space group P21/c with a = 11.4137(2) Å, b = 11.8877(2) Å, c = 23.4459(3) Å, β = 90.092(1)°, V = 3181.19(8) Å(3), and Z = 2 and contains well-ordered ammonium cations and [B7O9(OH)5](2-) anions and disordered B(OH)3 and H2O molecules linked by extensive H bonding. Expeditious solid-state formation of the heptaborate anion under ambient conditions has important implications for development of practical syntheses of industrially useful borates.

Modulation of TRAIL resistance in colon carcinoma cells: Different contributions of DR4 and DR5

International Nuclear Information System (INIS)

Geelen, Caroline MM van; Pennarun, Bodvael; Le, Phuong TK; Vries, Elisabeth GE de; Jong, Steven de

2011-01-01

rhTRAIL is a therapeutic agent, derived from the TRAIL cytokine, which induces apoptosis in cancer cells by activating the membrane death receptors 4 and 5 (DR4 and DR5). Here, we investigated each receptor's contribution to rhTRAIL sensitivity and rhTRAIL resistance. We assessed whether agonistic DR4 or DR5 antibodies could be used to circumvent rhTRAIL resistance, alone or in combination with various chemotherapies. Our study was performed in an isogenic model comprised of the SW948 human colon carcinoma cell line and its rhTRAIL resistant sub-line SW948-TR. Effects of rhTRAIL and agonistic DR4/DR5 antibodies on cell viability were measured using MTT assays and identification of morphological changes characteristic of apoptosis, after acridine orange staining. Sensitivity to the different death receptor ligands was stimulated using pretreatment with the cytokine IFN-gamma and the proteasome inhibitor MG-132. To investigate the mechanisms underlying the changes in rhTRAIL sensitivity, alterations in expression levels of targets of interest were measured by Western blot analysis. Co-immunoprecipitation was used to determine the composition of the death-inducing signalling complex at the cell membrane. SW948 cells were sensitive to all three of the DR-targeting agents tested, although the agonistic DR5 antibody induced only weak caspase 8 cleavage and limited apoptosis. Surprisingly, agonistic DR4 and DR5 antibodies induced equivalent DISC formation and caspase 8 cleavage at the level of their individual receptors, suggesting impairment of further caspase 8 processing upon DR5 stimulation. SW948-TR cells were cross-resistant to all DR-targeting agents as a result of decreased caspase 8 expression levels. Caspase 8 protein expression was restored by MG-132 and IFN-gamma pretreatment, which also re-established sensitivity to rhTRAIL and agonistic DR4 antibody in SW948-TR. Surprisingly, MG-132 but not IFN-gamma could also increase DR5-mediated apoptosis in SW948

Modulation of TRAIL resistance in colon carcinoma cells: Different contributions of DR4 and DR5

Directory of Open Access Journals (Sweden)

de Vries Elisabeth GE

2011-01-01

Full Text Available Abstract Background rhTRAIL is a therapeutic agent, derived from the TRAIL cytokine, which induces apoptosis in cancer cells by activating the membrane death receptors 4 and 5 (DR4 and DR5. Here, we investigated each receptor's contribution to rhTRAIL sensitivity and rhTRAIL resistance. We assessed whether agonistic DR4 or DR5 antibodies could be used to circumvent rhTRAIL resistance, alone or in combination with various chemotherapies. Methods Our study was performed in an isogenic model comprised of the SW948 human colon carcinoma cell line and its rhTRAIL resistant sub-line SW948-TR. Effects of rhTRAIL and agonistic DR4/DR5 antibodies on cell viability were measured using MTT assays and identification of morphological changes characteristic of apoptosis, after acridine orange staining. Sensitivity to the different death receptor ligands was stimulated using pretreatment with the cytokine IFN-gamma and the proteasome inhibitor MG-132. To investigate the mechanisms underlying the changes in rhTRAIL sensitivity, alterations in expression levels of targets of interest were measured by Western blot analysis. Co-immunoprecipitation was used to determine the composition of the death-inducing signalling complex at the cell membrane. Results SW948 cells were sensitive to all three of the DR-targeting agents tested, although the agonistic DR5 antibody induced only weak caspase 8 cleavage and limited apoptosis. Surprisingly, agonistic DR4 and DR5 antibodies induced equivalent DISC formation and caspase 8 cleavage at the level of their individual receptors, suggesting impairment of further caspase 8 processing upon DR5 stimulation. SW948-TR cells were cross-resistant to all DR-targeting agents as a result of decreased caspase 8 expression levels. Caspase 8 protein expression was restored by MG-132 and IFN-gamma pretreatment, which also re-established sensitivity to rhTRAIL and agonistic DR4 antibody in SW948-TR. Surprisingly, MG-132 but not IFN

Compatibility study of trans-1,4,5,8-tetranitro-1,4,5,8-tetraazadecalin (TNAD) with some energetic components and inert materials

International Nuclear Information System (INIS)

Yan Qilong; Li Xiaojiang; Zhang Laying; Li Jizhen; Li Hongli; Liu Ziru

2008-01-01

The compatibility of trans-1,4,5,8-tetranitro-1,4,5,8-tetraazadecalin (TNAD) with some energetic components and inert materials of solid propellants was studied by using the pressure DSC method where, cyclotetramethylenetetranitroamine (HMX), cyclotrimethylenetrinitramine (RDX), 1,4-dinitropiperazine (DNP), 1.25/1-NC/NG mixture, lead 3-nitro-1,2,4-triazol-5-onate (NTO-Pb), aluminum powder (Al, particle size = 13.6 μm) and N-nitrodihydroxyethylaminedinitrate (DINA) were used as energetic components and polyethylene glycol (PEG), polyoxytetramethylene-co-oxyethylene (PET), addition product of hexamethylene diisocyanate and water (N-100), 2-nitrodianiline (2-NDPA), 1,3-dimethyl-1,3-diphenyl urea (C 2 ), carbon black (C.B.), aluminum oxide (Al 2 O 3 ), cupric 2,4-dihydroxy-benzoate (β-Cu), cupric adipate (AD-Cu) and lead phthalate (φ-Pb) were used as inert materials. It was concluded that the binary systems of TNAD with NTO-Pb, RDX, PET and Al powder are compatible, and systems of TNAD with DINA and HMX are slightly sensitive, and with 2-NDPA, φ-Pb, β-Cu, AD-Cu and Al 2 O 3 are sensitive, and with PEG, N-100, C 2 and C.B. are incompatible. The impact and friction sensitivity data of the TNAD and TNAD in combination with the other energetic materials under present study was also obtained, and there was no consequential affiliation between sensitivity and compatibility

Preparation of La{sup 3+}/Zn{sup 2+}-doped BiVO{sub 4} nanoparticles and its enhanced visible photocatalytic activity

Energy Technology Data Exchange (ETDEWEB)

Hou, Yanhui; Yuan, Huili; Chen, Hang; Feng, Jiantao; Ding, Yan; Li, Liangchao [Zhejiang Normal University, Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Department of Chemistry, Jinhua (China)

2017-10-15

BiVO{sub 4} samples doped with different amounts of La{sup 3+} or Zn{sup 2+} ions have been synthesized successfully by a hydrothermal method, and their composition, microstructure and photocatalytic activity were characterized by means of modern analytical techniques. The results illustrated that these doped BiVO{sub 4} samples presented a better photocatalytic performance than the undoped BiVO{sub 4} sample, among which Bi{sub 0.92}La{sub 0.08}VO{sub 4} and Bi{sub 0.92}Zn{sub 0.08}VO{sub 4} exhibited the highest degradation efficiency. Under visible light illumination, their photocatalytic degradation on RhB was up to 95.4 and 98.56% in 60 min, respectively. In particular, the Bi{sub 0.92}La{sub 0.08}VO{sub 4} and Bi{sub 0.92}Zn{sub 0.08}VO{sub 4} had a good stability and still retained the photocatalytic activity of 93.7 and 94% after five cycling test. These results confirmed that the La{sup 3+}/Zn{sup 2+}-doped BiVO{sub 4} samples were a kind of efficient and stable visible-light-driven photocatalysts and had a promising application for the degradation of organic contaminant. (orig.)

Rare earth-transition metal indides with Lu{sub 5}Ni{sub 2}In{sub 4}-type structure

Energy Technology Data Exchange (ETDEWEB)

Zaremba, Roman; Hermes, Wilfried; Eul, Matthias; Poettgen, Rainer [Inst. fuer Anorganische und Analytische Chemie, Univ. Muenster (Germany)

2008-12-15

New intermetallic compounds RE{sub 5}T{sub 2}In{sub 4} (RE = Sc, Y, La-Nd, Sm, Gd-Tm, Lu; T = Rh, Ir) were synthesized by arc-melting of the elements or by induction melting of the elements in tantalum crucibles under flowing argon. The samples were characterized by X-ray powder diffraction. They crystallize with the orthorhombic Lu{sub 5}Ni{sub 2}In{sub 4}-type structure, space group Pbam, Z = 2, a 2: 1 intergrowth variant of CsCl and AlB{sub 2} related slabs of compositions InRE{sub 8} (distorted cubes) and RhRE{sub 6} (distorted trigonal prisms). Susceptibility measurements of Ce{sub 5}Ir{sub 2}In{sub 4} have revealed modified Curie-Weiss behavior above 70 K with an experimental magnetic moment of 2.45(1) {mu}{sub B} / Ce atom. The cerium magnetic moments order ferri- or ferromagnetically at T{sub C} = 7.1(2) K. (orig.)

Synthesis, Characterization and Antimicrobial Activity of Metal Chelates of 5-[4-Chloro phenyl(1, 3, 4thiadiazol-2-ylamino methylene]-8-hydroxy quinoline

Directory of Open Access Journals (Sweden)

Divyesh K. Patel

2009-01-01

Full Text Available 5-Chloromethyl-8-quinolinol was condensed stoichiometrically with 5-(4-chlorophenyl-(1,3,4 thiadiazol-2-ylamine in the presence of sodium bicarbonate. The resulting 5-[4-chlorophenyl-(1,3,4thiadiazol-2-ylamino methylene]-8-quinolinol (CTAQ was characterized by elemental analysis and spectral studies. The transition metal chelates viz. Cu2+, Ni2+, Co2+, Mn2+ and Zn2+ of CTAQ were prepared and characterized by metal-ligand (M:L ratio, IR and reflectance spectroscopies and magnetic properties. The antifungal activity of CTAQ and its metal chelates was screened against various fungi. The results show that all these samples are good antifungal agents.

Erektile Dysfunktion, Phosphodiesterase-5-Hemmer und KHK - die Sicht des Kardiologen

Directory of Open Access Journals (Sweden)

Schmid P

2004-01-01

Full Text Available Die erektile Dysfunktion (ED kommt vermehrt bei Patienten mit koronarer Herzkrankheit (KHK vor und wird üblicherweise mit Phosphodiesterase- 5-Hemmern (PDE-5-Hemmer wie Sildenafil, Vardenafil und Tadalafil behandelt. Dies geht mit einem systemischen Blutdruckabfall von bis zu 10 mmHg systolisch und bis 6 mmHg diastolisch einher. Die Herzfrequenz bleibt gleich oder steigt minimal an, das Doppelprodukt (RR sys x HF als Maß des myokardialen Sauerstoffverbrauches bleibt unverändert oder sinkt ab. Koronarangiographische Untersuchungen bei KHK-Patienten unter Sildenafil ergaben gegenüber Placebo keine Unterschiede in der Hämodynamik. Auch die Koronarreserve, die Blutflußgeschwindigkeit, der Durchmesser der Koronararterien, das Blutflußvolumen und der Koronargefäßwiderstand blieben unbeeinflußt. Die körperliche Leistungsfähigkeit wurde durch Sildenafil und Vardenafil nicht verändert. Eine kardiovaskuläre Exzeßmortalität liegt durch Einnahme von PDE-5-Hemmern nicht vor. Absolute Kontraindikation für eine Therapie mit PDE-5-Hemmern ist die gleichzeitige Gabe von NO-Donatoren (Nitrate, Molsidomin, Nitroprussid-Natrium, relative Kontraindikationen sind eine akute Koronarinsuffizienz, Herzinsuffizienz mit niedrigem Blutdruck, vorbestehende antihypertensive 3- bis 4-fach-Kombinationstherapie, Pharmaka, die den Abbau bzw. die Elimination von PDE-5-Hemmern reduzieren, sowie Antiarrhythmika der Klasse III.

Photocatalytic degradation of RhB over MgFe2O4/TiO2 composite materials

International Nuclear Information System (INIS)

Zhang Lei; He, Yiming; Wu Ying; Wu Tinghua

2011-01-01

Highlights: → Novel composite MgFe 2 O 4 /TiO 2 as catalyst. → Higher activity for the photodegradation of RhB under visible light irradiation. → Calcination temperature of catalyst has effect on photocatalytic activity. → Different photocatalysis mechanism under UV and visible light irradiation. - Abstract: MgFe 2 O 4 /TiO 2 (MFO/TiO 2 ) composite photocatalysts were successfully synthesized using a mixing-annealing method. The synthesized composites exhibited significantly higher photocatalytic activity than a naked semiconductor in the photodegradation of Rhodamine B. Under UV and visible light irradiation, the optimal percentages of doped MgFe 2 O 4 (MFO) were 2 wt.% and 3 wt.%, respectively. The effects of calcination temperature on photocatalytic activity were also investigated. The origin of the high level of activity was discussed based on the results of X-ray diffraction, UV-vis diffuse reflection spectroscopy, scanning electron microscopy, transmission electron microscopy, and nitrogen physical adsorption. The enhanced activity of the catalysts was mainly attributed to the synergetic effect between the two semiconductors, the band potential of which matched suitably.

Magnetic behaviour of nano-particles of Fe2.8Zn0.2O4

Indian Academy of Sciences (India)

Magnetic behaviour of nano-particles of Fe2.8Zn0.2O4. SUBHASH CHANDER, SEEMA LAKHANPAL, ANJALI KRISHNAMURTHY,. BIPIN K SRIVASTAVA and V K ASWAL∗. Department of Physics, University of Rajasthan, Jaipur 302 004, India. *Solid State Physics Division, Bhabha Atomic Research Centre, Mumbai 400 ...

Optical and magnetic properties of ZnO/ZnFe{sub 2}O{sub 4} nanocomposite

Energy Technology Data Exchange (ETDEWEB)

Zamiri, Reza, E-mail: reza.zamiri@tdt.edu.vn [Department for Management of Science and Technology Development, Ton Duc Thang University, Ho Chi Minh City (Viet Nam); Faculty of Electrical & Electronics Engineering, Ton Duc Thang University, Ho Chi Minh City (Viet Nam); Salehizadeh, S.A. [Physics Department (I3N), University of Aveiro, Campus Universitario de Santiago, Aveiro (Portugal); Ahangar, Hossein Abbastabar [Department of Chemistry, Faculty of Sciences, Najafabad Branch, Islamic Azad University, Najafabad (Iran, Islamic Republic of); Shabani, Mehdi; Rebelo, Avito [Department of Materials and Ceramic Engineering (DEMaC), University of Aveiro, Campus Santiago, Aveiro, 3810-193 (Portugal); Suresh Kumar, J.; Soares, M.J.; Valente, M.A. [Physics Department (I3N), University of Aveiro, Campus Universitario de Santiago, Aveiro (Portugal); Ferreira, J.M.F. [Department of Materials and Ceramic Engineering (DEMaC), University of Aveiro, Campus Santiago, Aveiro, 3810-193 (Portugal)

2017-05-01

ZnO/ZnFe{sub 2}O{sub 4} nanocomposite was prepared by a simple and low cost chemical precipitation method. The prepared composite was characterized by X-ray diffraction (XRD), energy-dispersive X-ray (EDX), Raman and Fourier Transform infrared spectroscopy (FTIR). The morphology of the prepared sample was studied by scanning electron microscopy (SEM). Photoluminescence (PL) emission of the sample has been investigated at different temperatures (10–300 K) in order to determine the effect of temperature on emission properties of the prepared composite. It was found that at low temperature, the samples show stronger emissions than those at room temperature. Magnetic properties of ZnO/ZnFe{sub 2}O{sub 4} nanocomposite was discussed in temperature range of 5–300 K using VSM measurement. The effective anisotropy constant K{sub eff}, extracted from the magnetization vs. magnetic field, M(B), experimental curve obtained at 5 K and using the law of saturation magnetization, was found to be 2.3 × 10{sup 6} erg/cm{sup 3}. The high value of anisotropy constant is attributed to the existence of uncompensated surface spin in our sample as well as the magnetocrystalline contribution (which depends on the inversion degree in ZnFe{sub 2}O{sub 4}). By using of a modified Langevin equation, the contribution of the surface spins was quantitatively calculated in different temperature higher than T{sub B}. It was found that as the temperature increases from 100 K to 300 K, the surface spins contribution in the total magnetization increases from 44% to 68%. - Highlights: • Fabrication of ZnO/ZnFe{sub 2}O{sub 4} nanocomposite by a simple and low cost method. • The sample show stronger emissions at low temperature than at room temperature. • The effective anisotropy constant K{sub eff}, was found to be 2.3 × 10{sup 6} erg/cm{sup 3}. • By increasing temperature from 100 K to 300 K, the surface spins contribution increases.

Konstruieren von Pkw-Karosserien: Grundlagen, Elemente und Baugruppen, Vorschriftenübersicht, Beispiele mit CATIA V4 und V5

Science.gov (United States)

Grabner, Jörg; Nothhaft, Richard

Die Faszination, die vom Auto ausgeht, ist und bleibt ungebrochen. Entsprechend interessant ist es, sich vor dem Hintergrund konventioneller Konstruktionstechniken über die virtuelle Produktentwicklung von Pkw-Karosserien an modernen CAD-Arbeitsplätzen informieren zu können. Die Autoren führen in die Grundlagen ein und zeigen anhand von Beispielen und zahlreichen Abbildungen, wie mit dem System CATIA der Rohbau sowie die Ausstattung innen und au=C3=9Fen konstruiert werden. Darüber hinaus wird das so genannte "Package" an Beispielen beschrieben, also das Management und die Harmonisierung der Anforderungen an die Bauräume (z.

Preparation and characterization of chitosan/ZnAl2O4 films

International Nuclear Information System (INIS)

Araujo, P.M.A.G.; Santos, P.T.A.; Rodrigues, P.A.; Costa, A.C.F.M.; Araujo, E.M.

2012-01-01

Chitosan films have been explored for biomedical application, as the chitosan to be, low toxicity, abundant in nature, show affinity for dispersion loads and high mechanical strength. On the other hand, ZnAl 2 O 4 has energy gap of approximately 3.8 eV, which makes it useful for use as photoelectric device ultraviolet. Thus, this work has as objective to prepare films of quitosana/ZnAl 2 O 4 in proportions of 5:1, 5:2, 5:3, 5:4 and evaluate the structural, morphological and thermals characteristics. To this end, ZnAl2O4 first nanoparticles (NPs) was deagglomerated and 325 mesh sieve and added to chitosan diluted in 1% acetic acid, and dried at 60°C. After drying, a solution of 1M sodium hydroxide was added to obtain a film with neutral pH. The films were characterized by XRD, SEM and TG. For all proportions evaluated it was verified the presence of ZnAl 2 O)4 and chitosan phases. By micrographs, it was observed that there was formation of agglomerates of ZnAl 2 O 4 NPs both on the surface of the films, the encapsulated in chitosan. In all samples the ratio 5:4 showed the greatest consistency both in relation to the film surface of the nanoparticles in the chitosan matrix. TG/DTA curves of quitosana/ZnAl 2 O 4 film for all the samples showed that for the concentration of 5:1 to 5:3 occurred three mass loss while for concentration of 5:2 to 5:4 were only two stages decomposition. (author)

Synthesis, single-crystal structure refinement and Fe/T site preference in the ternary borides Fe {sub x}T{sub 7-x}B{sub 3} (T = Ru, Rh; 0 < x {<=} 1.5)

Energy Technology Data Exchange (ETDEWEB)

Fokwa, Boniface P.T. [Institut fuer Anorganische Chemie, Rheinisch-Westfaelische Technische Hochschule Aachen, D-52056 Aachen (Germany); Dronskowski, Richard [Institut fuer Anorganische Chemie, Rheinisch-Westfaelische Technische Hochschule Aachen, D-52056 Aachen (Germany)]. E-mail: drons@HAL9000.ac.rwth-aachen.de

2007-01-31

Single crystals of the borides Fe {sub x}Rh{sub 7-x}B{sub 3} (1 < x < 1.5) and Fe {sub x}Ru{sub 7-x}B{sub 3} (0 < x < 1) have been synthesized by arc-melting the elements in a water-cooled copper crucible under argon atmosphere. The silver-like products, structurally characterized by single-crystal X-ray analysis, adopt the hexagonal Th{sub 7}Fe{sub 3} structure type (space group P6{sub 3} mc, no. 186) with Z = 2. Their structures consist of layers of boron-centered trigonal prisms of rhodium or ruthenium (Rh;Ru) and iron on the one side, and one-dimensional channels of face-sharing octahedral (Rh;Ru){sub 6} clusters on the other. Unlike in FeRh{sub 6}B{sub 3}, the iron substitution takes place at two (6c and 2b) of the three available rhodium/ruthenium positions, with a preference for the 6c site in the case of the Fe {sub x}Rh{sub 7-x}B{sub 3} compounds but not for Fe {sub x}Ru{sub 7-x}B{sub 3}.

Beperking koper- en zinkbelasting melkveehouderij : balansen voor koper en zink op 3 melkveebedrijven in Utrecht en op 30 bedrijven in studieclubs

NARCIS (Netherlands)

Smolders, E.A.A.

2008-01-01

In de Kaderrichtlijn Water worden beperkingen gesteld aan de hoeveelheid koper en zink in het oppervlaktewater. Een deel van het koper en zink in het water is afkomstig uit de landbouw, waarvan ook een deel uit de melkveehouderij. Op 3 melkveebedrijven in Utrecht is, in opdracht van LAMI, een balans

Photoaffinity labeling of pituitary GnRH receptors: significance of the position of photolabel on the ligand

International Nuclear Information System (INIS)

Nikolics, K.; Szonyi, E.; Ramachandran, J.

1988-01-01

Photoreactive derivatives of GnRH and its analogues were prepared by incorporation of the 2-nitro-4(5)-azidophenylsulfenyl [2,4(5)-NAPS] group into amino acid residues at position 1, 3, 6, or 8 of the decapeptide sequence. The modification of Trp 3 by the 2,4-NAPS group led to a complete loss of the luteinizing hormone (LH) releasing as well as LH-release-inhibiting activity of the peptide. The [D-Lys(2,4-NAPS)] 6 analog was a very potent agonist that, after covalent attachment by photoaffinity labeling, caused prolonged LH secretion at a submaximal rate. [Orn(2,4-NAPS)] 8 -GnRH, a full agonist with a relative potency of 7% of GnRH, after photoaffinity labeling caused prolonged maximal LH release from cultured pituitary cells. In contrast, [Orn(2,5-NAPS)] 8 -GnRH, although being equipotent with the 2,4-NAPS isomer in terms of LH releasing ability, was unable to cause prolonged LH release after photoaffinity labeling. Thus, [Orn(2,4-NAPS)] 8 GnRH is very effective photolabeling ligand of the functionally significant pituitary GnRH receptor. Based on this compound, a pituitary peptidase resistant derivative, D-Phe 6 , [Orn(2,4-NAPS)] 8 -GnRH-(1-9)-ethylamide, was synthesized. This derivative showed high-affinity binding to pituitary membranes with a K/sub d/ comparable to those of other GnRH analogues. A radioiodinated form of this peptide was used for pituitary GnRH-receptor labeling. This derivative labeled 59- and 57-kDa proteins in rat and 58- and 56-kDa proteins in bovine pituitary membrane preparations, respectively. This peptide also labeled pituitary GnRH receptors in the solubilized state and therefore appears to be a suitable ligand for the isolation and further characterization of the receptor

Bridging Binding Modes of Phosphine-Stabilized Nitrous Oxide to Zn(C6F5)2

NARCIS (Netherlands)

Neu, Rebecca C.; Otten, Edwin; Stephan, Douglas W.

2009-01-01

Reaction of [tBu3PN2O(B(C6H4F)3)] with 1, 1.5, or 2 equivalents of Zn(C6F5)2 affords the species [{tBu3PN2OZn(C6F5)2}2], [{tBu3PN2OZn(C6F5)2}2Zn(C6F5)2], and [tBu3PN2O{Zn(C6F5)2}2] displaying unique binding modes of Zn to the phosphine-stabilized N2O fragment.

Zinc(II PVC-based membrane sensor based on 5,6-benzo-4,7,13,16,21,24- hexaoxa-1,10-diazabicyclo[8,8,8]hexacos-5-ene

Directory of Open Access Journals (Sweden)

Zamani Hassan Ali

2006-01-01

Full Text Available The 5,6-benzo-4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8,8,8]hexacos-5-ene (BHDE was used as an excellent ionophore in construction of a Zn(II PVC-based membrane sensor. The best performance was obtained with a membrane composition of 30% poly(vinyl chloride, 64.5% nitrobenzen (NB, 2.5% BHDE and 3% sodium tetraphenylborate (NaTPB. This sensor shows very good selectivity and sensitivity towards zinc ion over a wide variety of cations, including alkali, alkaline earth, transition and heavy metal ions. The sensor revealed a great enhancement in selectivity coefficients for zinc ions, in comparison to the previously reported zinc sensors. The proposed sensor exhibits a Nernstian behavior (with slope of 29.1 ? 0.4 mV per decade over a wide concentration range (1.0 10-6-1.0 10-1 mol L-1 with a detection limit of 6.3 x10-7 mol L-1 (41.2 ng mL-1. It shows relatively fast response time, in the whole concentration range (< 10s, and can be used for at least 10 weeks in a pH range of 2.8-7.3. The proposed sensor was successfully used in direct determination of zinc ions in wastewater of industrial zinc electroplating companies, and also as an indicator electrode in titration with EDTA.

Yb valence state in Yb{sub 5}Rh{sub 4}Ge{sub 10}

Energy Technology Data Exchange (ETDEWEB)

Sato, Hitoshi; Arita, Masashi; Shimada, Kenya; Namatame, Hirofumi; Taniguchi, Masaki [Hiroshima Synchrotron Radiation Center, Hiroshima University, Higashi-Hiroshima (Japan); Utsumi, Yuki [Synchrotron SOLEIL, L' Orme des Merisiers, Gif-sur-Yvette (France); Katoh, Kenichi [Department of Applied Physics, National Defense Academy, Yokosuka (Japan); Mimura, Kojiro [Graduate School of Engineering, Osaka Prefecture University, Sakai (Japan); Ueda, Shigenori [Synchrotron X-ray Station at SPring-8, National Institute for Materials Science, Hyogo (Japan); Quantum Beam Unit, National Institute for Materials Science, Tsukuba (Japan); Yamaoka, Hitoshi [RIKEN SPring-8 Center, Hyogo (Japan); Rousuli, Awabaikeli [Graduate School of Science, Hiroshima University, Higashi-Hiroshima (Japan); Umeo, Kazunori [NBARD, Hiroshima University, Higashi-Hiroshima (Japan)

2017-06-15

Temperature- and pressure-dependent Yb valence state in Yb{sub 5}Rh{sub 4}Ge{sub 10} has been investigated by means of Yb 3d hard X-ray photoemission spectroscopy (HAXPES) and Yb L{sub 3} absorption spectroscopy (XAS). The mean Yb valence derived from the Yb 3d HAXPES is estimated to be ∝2.78 at 300 K and decreases to ∝2.74 at 20 K. On the other hand, the Yb valence deduced from the Yb L{sub 3} XAS at 300 K is almost constant with ∝2.81 in the pressure range between 9.2 and 34.7 GPa. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Aqueous hydrodechlorination of 4-chlorophenol over an Rh/reduced graphene oxide synthesized by a facile one-pot solvothermal process under mild conditions

International Nuclear Information System (INIS)

Ren, Yanlin; Fan, Guangyin; Wang, Chenyu

2014-01-01

Graphical abstract: The Rh nanoparticles/reduced graphene oxide (Rh NPs/RGO) nanocatalyst synthesized by a solvothermal technique showed high activity and stability for the hydrodechlorination of 4-chlorophenol under mild conditions. - Highlights: • Rh/RGO was synthesized through a one-pot polyol reduction of GO and RhCl 3 . • Complete HDC of 4-chlorophenol was obtained in aqueous phase without any additive. • The Rh/RGO exhibited an excellent catalytic performance for HDC reaction. - Abstract: Reduced graphene oxide (RGO) supported rhodium nanoparticles (Rh-NPs/RGO) was synthesized through one-pot polyol co-reduction of graphene oxide (GO) and rhodium chloride. The catalytic property of Rh-NPs/RGO was investigated for the aqueous phase hydrodechlorination (HDC) of 4-chlorophenol (4-CP). A complete conversion of 4-CP into high valued products of cyclohexanone (selectivity: 23.2%) and cyclohexanol (selectivity: 76.8%) was successfully achieved at 303 K and balloon hydrogen pressure in a short reaction time of 50 min when 1.5 g/L of 4-CP was introduced. By comparing with Rh-NPs deposited on the other supports, Rh-NPs/RGO delivered the highest initial rate (111.4 mmol/g Rh min) for 4-CP HDC reaction under the identical conditions. The substantial catalytic activity of Rh-NPs/RGO can be ascribed to the small and uniform particle size of Rh (average particle size was 1.7 ± 0.14 nm) on the surface of the RGO sheets and an electron-deficient state of Rh in the catalyst as a result of the strong interaction between the active sites and the surface function groups of RGO

Autocrine Acetylcholine, Induced by IL-17A via NFκB and ERK1/2 Pathway Activation, Promotes MUC5AC and IL-8 Synthesis in Bronchial Epithelial Cells

Directory of Open Access Journals (Sweden)

Angela Marina Montalbano

2016-01-01

Full Text Available IL-17A is overexpressed in the lung during acute neutrophilic inflammation. Acetylcholine (ACh increases IL-8 and Muc5AC production in airway epithelial cells. We aimed to characterize the involvement of nonneuronal components of cholinergic system on IL-8 and Muc5AC production in bronchial epithelial cells stimulated with IL-17A. Bronchial epithelial cells were stimulated with recombinant human IL-17A (rhIL-17A to evaluate the ChAT expression, the ACh binding and production, the IL-8 release, and the Muc5AC production. Furthermore, the effectiveness of PD098,059 (inhibitor of MAPKK activation, Bay11-7082 (inhibitor of IkBα phosphorylation, Hemicholinium-3 (HCh-3 (choline uptake blocker, and Tiotropium bromide (Spiriva® (anticholinergic drug was tested in our in vitro model. We showed that rhIL-17A increased the expression of ChAT, the levels of ACh binding and production, and the IL-8 and Muc5AC production in stimulated bronchial epithelial cells compared with untreated cells. The pretreatment of the cells with PD098,059 and Bay11-7082 decreased the ChAT expression and the ACh production/binding, while HCh-3 and Tiotropium decreased the IL-8 and Muc5AC synthesis in bronchial epithelial cells stimulated with rhIL-17A. IL-17A is involved in the IL-8 and Muc5AC production promoting, via NFκB and ERK1/2 pathway activation, the synthesis of ChAT, and the related activity of autocrine ACh in bronchial epithelial cells.

Hygroscopicity of internally mixed particles composed of (NH4)2SO4 and citric acid under pulsed RH change.

Science.gov (United States)

Shi, Xiao-Min; Wu, Feng-Min; Jing, Bo; Wang, Na; Xu, Lin-Lin; Pang, Shu-Feng; Zhang, Yun-Hong

2017-12-01

In this research, we applied a pulsed RH controlling system and a rapid scan vacuum FTIR spectrometer (PRHCS-RSVFTIR) to investigate hygroscopicity of internally mixed (NH 4 ) 2 SO 4 (AS)/citric acid (CA) particles. The water content and efflorescence ratio of AS in the particles and ambient relative humidity (RH) as a function of time were obtained with a subsecond time resolution. The hygroscopic behavior of AS aerosols in two different RH control processes (equilibrium and RH pulsed processes) showed that AS droplets crystallize with RH ranging from 42% to 26.5%. It was found that the half-life time ratio between the water content in the CA particles and the gas phase under RH pulsed change was greater than one under low RH conditions (humidity (ERH) of the mixed particles with AS/CA by molar ratio 3:1 was found between 22.7% and 5.9%, which was much lower than AS particles. No efflorescence process was observed for the 1:1 mixed particles, indicating that CA greatly suppressed nucleation of AS. Our results have shown that the PRHCS-RSVFTIR is effective to simulate hygroscopicity and water transport of aerosols under fast variations in RH in atmosphere. Copyright © 2017 Elsevier Ltd. All rights reserved.

Environmental application of millimetre-scale sponge iron (s-Fe"0) particles (IV): New insights into visible light photo-Fenton-like process with optimum dosage of H_2O_2 and RhB photosensitizers

International Nuclear Information System (INIS)

Ju, Yongming; Yu, Yunjiang; Wang, Xiaoyan; Xiang, Mingdeng; Li, Liangzhong; Deng, Dongyang; Dionysiou, Dionysios D.

2017-01-01

Highlights: • Synergistic action of Rhodamine B (RhB), visible light, H_2O_2 and s-Fe"0 is essential. • The complexes of RhB and Fe"3"+ eject one electron via ligand-to-metal charge-transfer. • RhB assists the photo-Fenton-like removal of tetrabromobisphenol A (TBBPA). - Abstract: In this study, we firstly develop the photo-Fenton-like system with millimetric sponge iron (s-Fe"0), H_2O_2, visible light (vis, λ ≥ 420 nm) and rhodamine B (RhB), and present a comprehensive study concerning the mechanism. Thus, we investigate (1) the adsorption of RhB onto s-Fe"0, (2) the photo-Fenton-like removal of RhB over iron oxides generated from the corrosion of s-Fe"0, (3) the homogeneous photo-Fenton removal of RhB over Fe"2"+ or Fe"3"+, (4) the Fe"3"+-RhB complexes, and (5) the photo-Fenton-like removal of tetrabromobisphenol A (TBBPA). The results show that neither the adsorption process over s-Fe"0 nor the photo-Fenton-like process over FeOOH, Fe_3O_4 and Fe_2O_3, achieved efficient removal of RhB. For comparison, in homogeneous photo-Fenton process, the presence of Fe"3"+ ions, rather than Fe"2"+ ions, effectively eliminated RhB. Furthermore, the UV–vis spectra showing new absorbance at ∼ 285 nm indicate the complexes of RhB and Fe"3"+ ions, adopting vis photons to form excited state and further eject one electron via ligand-to-metal charge-transfer to activate H_2O_2. Additionally, efficient TBBPA removal was obtained only in the presence of RhB. Accordingly, the s-Fe"0– based photo-Fenton-like process assisted with dyestuff wastewater is promising for removing a series of persistent organic pollutants.

Periodontal wound healing/regeneration following implantation of recombinant human growth/differentiation factor-5 (rhGDF-5) in an absorbable collagen sponge carrier into one-wall intrabony defects in dogs: a dose-range study.

Science.gov (United States)

Kim, Tae-Gyun; Wikesjö, Ulf M E; Cho, Kyoo-Sung; Chai, Jung-Kiu; Pippig, Susanne D; Siedler, Michael; Kim, Chong-Kwan

2009-07-01

Recombinant human growth/differentiation factor-5 (rhGDF-5) is being evaluated as a candidate therapy in support of periodontal regeneration. The objective of this study was to evaluate cementum and alveolar bone formation, and aberrant healing events following surgical implantation of rhGDF-5 in an absorbable collagen sponge (ACS) carrier using an established periodontal defect model. Bilateral 4 x 5 mm (width x depth), one-wall, critical-size, intrabony periodontal defects were surgically created at the mandibular second and fourth pre-molar teeth in 15 Beagle dogs. Five animals received 1 microg/defect and five animals 20 microg/defect rhGDF-5 in unilateral defect sites. Contralateral sites received treatments reported elsewhere. Five animals received rhGDF-5/ACS with 0 (buffer control) and 100 microg/defect rhGDF-5 in contralateral defect sites. The animals were euthanized at 8 weeks post-surgery for histologic and histometric evaluation. Surgical implantation of rhGDF-5 stimulated significant periodontal regeneration. Cementum formation was significantly enhanced in sites implanted with rhGDF-5 (1 and 100 microg) compared with control (phealing/regeneration in intrabony periodontal defects without complications.

Colossal thermoelectric power factor in K7/8RhO2

KAUST Repository

Saeed, Yasir

2012-04-12

The thermoelectric properties of the layered oxides KxRhO 2 (x = 1/2 and 7/8) are investigated by means of the electronic structure, as determined by ab inito calculations and Boltzmann transport theory. In general, the electronic structure of K xRhO 2 is similar to Na xCoO 2, but with strongly enhanced transport. K 7/8RhO 2 exceeds the ultrahigh power factor of Na 0.88CoO 2 reported previously by more than 50%. The roles of the cation concentration and the lattice parameters in the transport properties in this class of compounds are explained. © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Deposition of CdS nanoparticles on MIL-53(Fe) metal-organic framework with enhanced photocatalytic degradation of RhB under visible light irradiation

Energy Technology Data Exchange (ETDEWEB)

Hu, Longxing, E-mail: hulxhhhb@shu.edu.cn [School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444 (China); Deng, Guihua [School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444 (China); Lu, Wencong [College of Sciences, Shanghai University, Shanghai 200444 (China); Pang, Siwei; Hu, Xing [School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444 (China)

2017-07-15

Graphical abstract: The CdS/MIL-53(Fe) photocatalyst has been synthesized by a facile two-step solvothermal method and applied for photocatalytic degradation of organic pollutant RhB under visible light irradiation. - Highlights: • A novel CdS/MIL-53(Fe) photocatalyst was successfully synthesized via a facile two-step solvothermal method. • CdS/MIL-53(Fe) exhibited an enhanced visible-light photocatalytic degradation of RhB in water. • The mechanisms for the formation of CdS/MIL-53(Fe) and photocatalytic degradation of RhB were proposed. - Abstract: A novel composite, CdS/MIL-53(Fe), was successfully fabricated via a facile solvothermal method and characterized with XRD, SEM, TEM, XPS, FT-IR and UV–vis DRS. The results showed that the fabrication was able to result in a good dispersion of CdS nanoparticles onto MIL-53(Fe). The photocatalytic activities of the as-synthesized composite were investigated through the degradation of Rhodamine B (RhB) in water under visible light irradiation. It was found that the composite prepared at the mass ratio of CdS to MIL-53(Fe) of 1.5:1 displayed the highest photocatalytic activity. An approximately 92.5% of photocatalytic degradation of RhB was achieved at 0.5 g/L of 1.5-CdS/MIL dosage, 10 mg/L of initial RhB concentration and 23 °C of reaction temperature under visible light irradiation. The RhB photocatalytic degradation followed well the first-order kinetics equation and the increased catalyst dosage and optimal initial RhB concentration were responsible for the enhanced photocatalytic degradation. Quenching tests revealed that the predominant free radicals in the CdS/MIL-(53)-RhB{sub aq}-visible light system was O{sub 2}{sup −}·; nevertheless, h{sup +} and ·OH also contributed to a certain degree. The enhanced photocatalytic performance was ascribed to the formation of heterojunction structure between CdS and MIL-53(Fe) which significantly suppressed the recombination of photogenerated electron-hole pairs

Deposition of CdS nanoparticles on MIL-53(Fe) metal-organic framework with enhanced photocatalytic degradation of RhB under visible light irradiation

International Nuclear Information System (INIS)

Hu, Longxing; Deng, Guihua; Lu, Wencong; Pang, Siwei; Hu, Xing

2017-01-01

Graphical abstract: The CdS/MIL-53(Fe) photocatalyst has been synthesized by a facile two-step solvothermal method and applied for photocatalytic degradation of organic pollutant RhB under visible light irradiation. - Highlights: • A novel CdS/MIL-53(Fe) photocatalyst was successfully synthesized via a facile two-step solvothermal method. • CdS/MIL-53(Fe) exhibited an enhanced visible-light photocatalytic degradation of RhB in water. • The mechanisms for the formation of CdS/MIL-53(Fe) and photocatalytic degradation of RhB were proposed. - Abstract: A novel composite, CdS/MIL-53(Fe), was successfully fabricated via a facile solvothermal method and characterized with XRD, SEM, TEM, XPS, FT-IR and UV–vis DRS. The results showed that the fabrication was able to result in a good dispersion of CdS nanoparticles onto MIL-53(Fe). The photocatalytic activities of the as-synthesized composite were investigated through the degradation of Rhodamine B (RhB) in water under visible light irradiation. It was found that the composite prepared at the mass ratio of CdS to MIL-53(Fe) of 1.5:1 displayed the highest photocatalytic activity. An approximately 92.5% of photocatalytic degradation of RhB was achieved at 0.5 g/L of 1.5-CdS/MIL dosage, 10 mg/L of initial RhB concentration and 23 °C of reaction temperature under visible light irradiation. The RhB photocatalytic degradation followed well the first-order kinetics equation and the increased catalyst dosage and optimal initial RhB concentration were responsible for the enhanced photocatalytic degradation. Quenching tests revealed that the predominant free radicals in the CdS/MIL-(53)-RhB aq -visible light system was O 2 − ·; nevertheless, h + and ·OH also contributed to a certain degree. The enhanced photocatalytic performance was ascribed to the formation of heterojunction structure between CdS and MIL-53(Fe) which significantly suppressed the recombination of photogenerated electron-hole pairs. Moreover, the

Trennung und Rekombination von Ladungsträgern in Solarzellen mit nanostrukturierter ZnO-Elektrode

OpenAIRE

Tornow, Julian

2010-01-01

In dieser Arbeit werden Elektroden aus hydrothermal auf leitfähigem Glassubstrat (Leitglas) abgeschiedenen ZnO-Nanostangen betrachtet. Die Elektroden selbst sind für sichtbares Licht transparent und werden für eine Anwendung als Solarzelle mit einer lichtabsorbierenden Schicht sensibilisiert; hier sind das entweder metallorganische Farbstoffmoleküle (N3) oder eine nur wenige Nanometer dicke Schicht aus Indiumsulfid. Für die elektrische Kontaktierung der sensibilisierten Elektrode wird entwed...

Spectroscopic ellipsometry study of Cu{sub 2}ZnSnSe{sub 4} bulk crystals

Energy Technology Data Exchange (ETDEWEB)

León, M., E-mail: maximo.leon@uam.es; Lopez, N.; Merino, J. M.; Caballero, R. [Department of Applied Physics M12, Universidad Autónoma de Madrid, Madrid (Spain); Levcenko, S.; Gurieva, G. [Helmholtz-Zentrum Berlin fuer Materialien und Energie, Berlin (Germany); Serna, R. [Laser Processing Group, Instituto de Optica, CSIC, Serrano 121, 28006 Madrid (Spain); Bodnar, I. V. [Department of Chemistry, Belarusian State University of Informatics and Radioelectronics, Minsk (Belarus); Nateprov, A.; Guc, M.; Arushanov, E. [Institute of Applied Physics, Academy of Sciences of Moldova, Chisinau MD 2028 (Moldova, Republic of); Schorr, S. [Helmholtz-Zentrum Berlin fuer Materialien und Energie, Berlin (Germany); Institute of Geological Sciences, Free University Berlin, Malteserstr. 74-100, Berlin (Germany); Perez-Rodriguez, A. [IREC, Catalonia Institute for Energy Research, C. Jardins de les Dones de Negre 1, 08930 Sant Adrià del Besòs (Barcelona) (Spain); IN2UB, Departament d' Electrònica, Universitat de Barcelona, Martí i Franquès 1, 08028 Barcelona (Spain)

2014-08-11

Using spectroscopic ellipsometry we investigated and analyzed the pseudo-optical constants of Cu{sub 2}ZnSnSe{sub 4} bulk crystals, grown by the Bridgman method, over 0.8–4.5 eV photon energy range. The structures found in the spectra of the complex pseudodielectric functions were associated to E{sub 0}, E{sub 1A}, and E{sub 1B} interband transitions and were analyzed in frame of the Adachi's model. The interband transition parameters such as strength, threshold energy, and broadening were evaluated by using the simulated annealing algorithm. In addition, the pseudo-complex refractive index, extinction coefficient, absorption coefficient, and normal-incidence reflectivity were derived over 0.8–4.5 eV photon energy range.

A putative SUMO interacting motif in the B30.2/SPRY domain of rhesus macaque TRIM5α important for NF-κB/AP-1 signaling and HIV-1 restriction

Directory of Open Access Journals (Sweden)

Marie-Édith Nepveu-Traversy

2016-01-01

Full Text Available TRIM5α from the rhesus macaque (TRIM5αRh is a restriction factor that shows strong activity against HIV-1. TRIM5αRh binds specifically to HIV-1 capsid (CA through its B30.2/PRYSPRY domain shortly after entry of the virus into the cytoplasm. Recently, three putative SUMO interacting motifs (SIMs have been identified in the PRYSPRY domain of human and macaque TRIM5α. However, structural modeling of this domain suggested that two of them were buried in the hydrophobic core of the protein, implying that interaction with SUMO was implausible, while the third one was not relevant to restriction. In light of these results, we re-analyzed the TRIM5αRh PRYSPRY sequence and identified an additional putative SIM (435VIIC438 which we named SIM4. This motif is exposed at the surface of the PRYSPRY domain, allowing potential interactions with SUMO or SUMOylated proteins. Introducing a double mutation in SIM4 (V435K, I436K did not alter stability, unlike mutations in SIM1. SIM4-mutated TRIM5αRh failed to bind HIV-1CA and lost the ability to restrict this virus. Accordingly, SIM4 undergoes significant variation among primates and substituting this motif with naturally occurring SIM4 variants affected HIV-1 restriction by TRIM5αRh, suggesting a direct role in capsid recognition. Interestingly, SIM4-mutated TRIM5αRh also failed to activate NF-κB and AP-1-mediated transcription. Although there is no direct evidence that SIM4 is involved in direct interaction with SUMO or a SUMOylated protein, mutating this motif strongly reduced co-localization of TRIM5αRh with SUMO-1 and with PML, a SUMOylated nuclear protein. In conclusion, this new putative SIM is crucial for both direct interaction with incoming capsids and for NF-κB/AP-1 signaling. We speculate that the latter function is mediated by interactions of SIM4 with a SUMOylated protein involved in the NF-κB/AP-1 signaling pathways.

26 CFR 5c.168(f)(8)-4 - Minimum investment of lessor.

Science.gov (United States)

2010-04-01

... 26 Internal Revenue 14 2010-04-01 2010-04-01 false Minimum investment of lessor. 5c.168(f)(8)-4....168(f)(8)-4 Minimum investment of lessor. (a) Minimum investment. Under section 168(f)(8)(B)(ii), an... has a minimum at risk investment which, at the time the property is placed in service under the lease...

Effect of Rh oxide as a cocatalyst over Bi{sub 0.5}Y{sub 0.5}VO{sub 4} on photocatalytic overall water splitting

Energy Technology Data Exchange (ETDEWEB)

Chen, Wei, E-mail: chanwee@henu.edu.cn [College of Chemistry and Chemical Engineering, Henan University, Kaifeng 475004, Henan (China); Yang, Bingbing; Yu, Qingtao; Mao, Liqun [College of Chemistry and Chemical Engineering, Henan University, Kaifeng 475004, Henan (China); Fan, Zeyun [Research Center for Combustion and Environmental Technology, Shanghai Jiao Tong University, Shanghai 200240 (China); Wang, Qizhao [College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070 (China); Shangguan, Wenfeng, E-mail: shangguan@sjtu.edu.cn [Research Center for Combustion and Environmental Technology, Shanghai Jiao Tong University, Shanghai 200240 (China)

2015-11-15

Graphical abstract: - Highlights: • The effect of cocatalysts as active sites for water splitting was investigated. • Rh{sub 2}O{sub 3} was found to give the highest photocatalytic activity. • Compared to Pt, NiO, Rh{sub 2}O{sub 3} can reduce more overpotential of O{sub 2} evolution. • Rh{sub 2}O{sub 3} also promote the separation of electrons and holes apparently. - Abstract: Pt, Rh{sub 2}O{sub 3}, NiO nanoparticles as cocatalysts were loaded on BYV solid solution photocatalysts by an impregnation method to promote photocatalytic activity for overall water splitting. The cocatalysts loading could enhance the photocatalytic activity significantly. The (photo)electrochemical measurements and HR-TEM, PL analyses revealed that the effect of cocatalysts acted as active sites depended on the efficient separation of photoinduced charge carriers as well as the reduction of the overpotential of O{sub 2} evolution. Among the cocatalysts in this study, Rh{sub 2}O{sub 3} was found to give the highest photocatalytic activity. This is because, compared to Pt and NiO, Rh{sub 2}O{sub 3} nanoparticles are able to not only reduce more overpotential of O{sub 2} evolution, but also extremely promote the separation of electrons and holes. 0.5 wt% Rh{sub 2}O{sub 3}/BYV exhibited the highest photocatalytic activity for H{sub 2} and O{sub 2} evolution, reaching 104.4 μmol/h and 50.9 μmol/h, respectively. The present work will be useful to instruct cocatalyst loading for obtaining the photocatalysts with high photocatalytic activity for overall water splitting.

Molecular structures and excited states of CpM(CO)(2) (Cp = eta(5)-C(5)H(5); M = Rh, Ir) and [Cl(2)Rh(CO)(2)](-). Theoretical evidence for a competitive charge transfer mechanism.

Science.gov (United States)

Hu, Zhenming; Boyd, Russell J; Nakatsuji, Hiroshi

2002-03-20

Molecular structures and excited states of CpM(CO)(2) (Cp = eta(5)-C(5)H(5); M = Rh, Ir) and [Cl(2)Rh(CO)(2)](-) complexes have been investigated using the B3LYP and the symmetry-adapted cluster (SAC)/SAC-configuration interaction (SAC-CI) theoretical methods. All the dicarbonyl complexes have singlet ground electronic states with large singlet-triplet separations. Thermal dissociations of CO from the parent dicarbonyls are energetically unfavorable. CO thermal dissociation is an activation process for [Cl(2)Rh(CO)(2)](-) while it is a repulsive potential for CpM(CO)(2). The natures of the main excited states of CpM(CO)(2) and [Cl(2)Rh(CO)(2)](-) are found to be quite different. For [Cl(2)Rh(CO)(2)](-), all the strong transitions are identified to be metal to ligand CO charge transfer (MLCT) excitations. A significant feature of the excited states of CpM(CO)(2) is that both MLCT excitation and a ligand Cp to metal and CO charge transfer excitation are strongly mixed in the higher energy states with the latter having the largest oscillator strength. A competitive charge transfer excited state has therefore been identified theoretically for CpRh(CO)(2) and CpIr(CO)(2). The wavelength dependence of the quantum efficiencies for the photoreactions of CpM(CO)(2) reported by Lees et al. can be explained by the existence of two different types of excited states. The origin of the low quantum efficiencies for the C-H/S-H bond activations of CpM(CO)(2) can be attributed to the smaller proportion of the MLCT excitation in the higher energy states.

Transport and NMR characteristics of the skutterudite-related compound Ca3Rh4Sn13

Science.gov (United States)

Tseng, C. W.; Kuo, C. N.; Li, B. S.; Wang, L. M.; Gippius, A. A.; Kuo, Y. K.; Lue, C. S.

2018-02-01

We report the electronic properties of the Yb3Rh4Sn13-type single crystalline Ca3Rh4Sn13 by means of the electrical resistivity, Hall coefficient, Seebeck coefficient, thermal conductivity, as well as 119Sn nuclear magnetic resonance (NMR) measurements. The negative sign of the Hall coefficient and Seebeck coefficient at low temperatures suggests that the n-type carriers dominate the electrical transport in Ca3Rh4Sn13, in contrast to the observations in Sr3Rh4Sn13 which has a p-type conduction. Such a finding indicates a significant difference in the electronic features between these two stannides. Furthermore, we analyzed the temperature-dependent 119Sn NMR spin-lattice relaxation rate for Ca3Rh4Sn13, (Sr0.7Ca0.3)3Rh4Sn13, and Sr3Rh4Sn13 to examine the change of the electronic Fermi-level density of states (DOS) in (Sr1-xCax)3Rh4Sn13. It indicates that the Sn 5s partial Fermi-level DOS enhances with increasing the Ca content, being consistent with the trend of the superconducting temperature. Since the total Fermi-level DOS usually obeys the same trend of the partial Fermi-level DOS, the NMR analysis provides microscopic evidence for the correlation between the electronic DOS and superconductivity of the (Sr1-xCax)3Rh4Sn13 system.

Analysis of Etched CdZnTe Substrates

Science.gov (United States)

Benson, J. D.; Bubulac, L. O.; Jaime-Vasquez, M.; Lennon, C. M.; Arias, J. M.; Smith, P. J.; Jacobs, R. N.; Markunas, J. K.; Almeida, L. A.; Stoltz, A.; Wijewarnasuriya, P. S.; Peterson, J.; Reddy, M.; Jones, K.; Johnson, S. M.; Lofgreen, D. D.

2016-09-01

State-of-the-art as-received (112)B CdZnTe substrates have been examined for surface impurity contamination and polishing residue. Two 4 cm × 4 cm and one 6 cm × 6 cm (112)B state-of-the-art as-received CdZnTe wafers were analyzed. A maximum surface impurity concentration of Al = 1.7 × 1015 atoms cm-2, Si = 3.7 × 1013 atoms cm-2, Cl = 3.12 × 1015 atoms cm-2, S = 1.7 × 1014 atoms cm-2, P = 1.1 × 1014 atoms cm-2, Fe = 1.0 × 1013 atoms cm-2, Br = 1.2 × 1014 atoms cm-2, and Cu = 4 × 1012 atoms cm-2 was observed on the as-received CdZnTe wafers. CdZnTe particulates and residual SiO2 polishing grit were observed on the surface of the as-received (112)B CdZnTe substrates. The polishing grit/CdZnTe particulate density on CdZnTe wafers was observed to vary across a 6 cm × 6 cm wafer from ˜4 × 107 cm-2 to 2.5 × 108 cm-2. The surface impurity and damage layer of the (112)B CdZnTe wafers dictate that a molecular beam epitaxy (MBE) preparation etch is required. The contamination for one 4 cm × 4 cm and one 6 cm × 6 cm CdZnTe wafer after a standard MBE Br:methanol preparation etch procedure was also analyzed. A maximum surface impurity concentration of Al = 2.4 × 1015 atoms cm-2, Si = 4.0 × 1013 atoms cm-2, Cl = 7.5 × 1013 atoms cm-2, S = 4.4 × 1013 atoms cm-2, P = 9.8 × 1013 atoms cm-2, Fe = 1.0 × 1013 atoms cm-2, Br = 2.9 × 1014 atoms cm-2, and Cu = 5.2 × 1012 atoms cm-2 was observed on the MBE preparation-etched CdZnTe wafers. The MBE preparation-etched surface contamination consists of Cd(Zn)Te particles/flakes. No residual SiO2 polishing grit was observed on the (112)B surface.

Standard enthalpies of formation of selected Rh{sub 2}YZ Heusler compounds

Energy Technology Data Exchange (ETDEWEB)

Yin, Ming, E-mail: myin1@hawk.iit.edu; Nash, Philip

2015-11-25

The standard enthalpies of formation (Δ{sub f}H°) of selected ternary Rh-based Rh{sub 2}YZ (Y = Cu, Fe, Mn, Ni, Ru, Ti, V; Z = Al, Ga, In, Si, Ge, Sn) compounds were measured using high temperature direct reaction calorimetry. The measured standard enthalpies of formation (in kJ/mol of atoms) are, for the Heusler compound Rh{sub 2}MnSn (−40.1 ± 3.6), for the B2-structured compounds: Rh{sub 2}FeAl (−48.5 ± 2.9); Rh{sub 2}MnAl (−72.4 ± 2.7); Rh{sub 2}MnGa (−55.3 ± 2.0); Rh{sub 2}MnIn (−35.3 ± 1.9), for the tetragonal compounds: Rh{sub 2}FeSn (−28.9 ± 1.3); Rh{sub 2}TiAl (−97.6 ± 2.2); Rh{sub 2}TiGa (−79.0 ± 1.8); Rh{sub 2}TiSn (−74.7 ± 3.1). Values are compared with those from first principles calculations in published papers and the Open Quantum Materials Database (OQMD). Lattice parameters of these compounds are determined using X-ray diffraction analysis (XRD). Microstructures were characterized using scanning electron microscopy (SEM) and Energy Dispersive Spectroscopy (EDS). - Highlights: • Standard enthalpies of formation of Rh{sub 2}YZ were measured using a drop calorimeter. • Measured enthalpies agree with first principles data in general. • Lattice parameters and related phase relationships were consistent with literature data. • Rh{sub 2}TiSn of tI8 structure were reported for the first time.

Hierarchical nanoflowers assembled with Au nanoparticles decorated ZnO nanosheets toward enhanced photocatalytic properties

DEFF Research Database (Denmark)

Yu, Cuiyan; Yu, Yanlong; Xu, Tao

2017-01-01

Hierarchical nanoflowers assembled with Au nanoparticles (NPs) decorated ZnO nanosheets (Au-ZnO nanosheet flowers, AZNSFs) were successful synthesized. The AZNSFs showed more efficient activity to photodegradation of RhB than that of pure ZnO nanosheet flowers and commercial ZnO nanopowders. The ...

Structure and Electronic Properties of Neutral and Negatively Charged RhBn Clusters (n = 3-10): A Density Functional Theory Study.

Science.gov (United States)

Li, Peifang; Mei, Tingting; Lv, Linxia; Lu, Cheng; Wang, Weihua; Bao, Gang; Gutsev, Gennady L

2017-08-31

The geometrical structure and electronic properties of the neutral RhB n and singly negatively charged RhB n - clusters are obtained in the range of 3 ≤ n ≤ 10 using the unbiased CALYPSO structure search method and density functional theory (DFT). A combination of the PBE0 functional and the def2-TZVP basis set is used for determining global minima on potential energy surfaces of the Rh-doped B n clusters. The photoelectron spectra of the anions are simulated using the time-dependent density functional theory (TD-DFT) method. Good agreement between our simulated and experimentally obtained photoelectron spectra for RhB 9 - provides support to the validity of our theoretical method. The relative stabilities of the ground-state RhB n and RhB n - clusters are estimated using the calculated binding energies, second-order total energy differences, and HOMO-LUMO gaps. It is found that RhB 7 and RhB 8 - are the most stable species in the neutral and anionic series, respectively. The chemical bonding analysis reveals that the RhB 8 - cluster possesses two sets of delocalized σ and π bonds. In both cases, the Hückel 4N + 2 rule is fulfilled and this cluster possesses both σ and π aromaticities.

Structural characterization, morphology and magnetic ferrite Ni_0_,_4Zn_0_,_5Fe_2Cu_0_,_1O_4

International Nuclear Information System (INIS)

Santos, P.T.A.; Fernandes, P.C.; Santos, P.T.A.; Costa, A.C.F.M.

2011-01-01

In this work the system Ni_0_,_4Zn_0_,_5Fe_2Cu_0_,_1O_4 was obtained by combustion reaction using urea as fuel in order to evaluate their structural characteristics, and morphological imaging. The resulting samples were characterized by XRD, BET, SEM / EDS and magnetic measurements. The synthesis by combustion reaction was effective for producing samples of ferrites with crystallite size 13 nm. The X-ray diffraction showed the major phase of the inverse spinel and traces of ZnO second phase. The resulting morphology showed the formation of soft agglomerates with interparticle porosity, and mapping by SEM / EDS indicated a good distribution of elements Ni, Cu, Zn, Fe and O constituent of ferrite. The ferrite showed superparamagnetic behavior with a value of saturation magnetization of 5.60 emu / g. (author)

Qatar Exoplanet Survey : Qatar-3b, Qatar-4b, and Qatar-5b

Science.gov (United States)

Alsubai, Khalid; Mislis, Dimitris; Tsvetanov, Zlatan I.; Latham, David W.; Bieryla, Allyson; Buchhave, Lars A.; Esquerdo, Gilbert A.; Bramich, D. M.; Pyrzas, Stylianos; Vilchez, Nicolas P. E.; Mancini, Luigi; Southworth, John; Evans, Daniel F.; Henning, Thomas; Ciceri, Simona

2017-04-01

We report the discovery of Qatar-3b, Qatar-4b, and Qatar-5b, three new transiting planets identified by the Qatar Exoplanet Survey. The three planets belong to the hot Jupiter family, with orbital periods of {P}{{Q}3{{b}}} = 2.50792 days, {P}{{Q}4{{b}}} = 1.80539 days, and {P}{{Q}5{{b}}} = 2.87923 days. Follow-up spectroscopic observations reveal the masses of the planets to be {M}{{Q}3{{b}}} = 4.31 ± 0.47 {M}{{J}}, {M}{{Q}4{{b}}} = 6.10 ± 0.54 {M}{{J}}, and {M}{{Q}5{{b}}} = 4.32 ± 0.18 {M}{{J}}, while model fits to the transit light curves yield radii of {R}{{Q}3{{b}}} = 1.096 ± 0.14 {R}{{J}}, {R}{{Q}4{{b}}} = 1.135 ± 0.11 {R}{{J}}, and {R}{{Q}5{{b}}} = 1.107 ± 0.064 {R}{{J}}. The host stars are low-mass main sequence stars with masses and radii M Q3 = 1.145 ± 0.064 M ⊙, M Q4 = 0.896 ± 0.048 M ⊙, M Q5 = 1.128 ± 0.056 M ⊙ and R Q3 = 1.272 ± 0.14 R ⊙, R Q4 = 0.849 ± 0.063 R ⊙, and R Q5 = 1.076 ± 0.051 R ⊙ for Qatar-3, 4, and 5 respectively. The V magnitudes of the three host stars are V Q3 = 12.88, V Q4 = 13.60, and V Q5 = 12.82. All three new planets can be classified as heavy hot Jupiters (M > 4 M J).

Direct evidence for the first-order phase transition at the lower critical temperature in Er/sub 1-x/Ho/sub x/Rh4B4

International Nuclear Information System (INIS)

Lachal, B.; Ishikawa, M.; Junod, A.; Muller, J.

1982-01-01

Using a heat-pulse and a relaxation technique, we have performed an extensive calorimetric investigation on the reetrant superconductors Er/sub 1-x/Ho/sub x/Rh 4 B 4 (x = 0.4 and 0.6) around their lower critical temperature. These experiments revealed a supercooling effect and thermal hystersis, thus establishing the first-order nature of the transition. Based on the measurement of the latent heat, our thermodynamic analysis suggests that the onset of ferromagnetism is lowered by only 55 mK due to the competing superconducting phase. Results of magnetization and ac susceptibility experiments on these compounds are also included

Deposition of CdS nanoparticles on MIL-53(Fe) metal-organic framework with enhanced photocatalytic degradation of RhB under visible light irradiation

Science.gov (United States)

Hu, Longxing; Deng, Guihua; Lu, Wencong; Pang, Siwei; Hu, Xing

2017-07-01

A novel composite, CdS/MIL-53(Fe), was successfully fabricated via a facile solvothermal method and characterized with XRD, SEM, TEM, XPS, FT-IR and UV-vis DRS. The results showed that the fabrication was able to result in a good dispersion of CdS nanoparticles onto MIL-53(Fe). The photocatalytic activities of the as-synthesized composite were investigated through the degradation of Rhodamine B (RhB) in water under visible light irradiation. It was found that the composite prepared at the mass ratio of CdS to MIL-53(Fe) of 1.5:1 displayed the highest photocatalytic activity. An approximately 92.5% of photocatalytic degradation of RhB was achieved at 0.5 g/L of 1.5-CdS/MIL dosage, 10 mg/L of initial RhB concentration and 23 °C of reaction temperature under visible light irradiation. The RhB photocatalytic degradation followed well the first-order kinetics equation and the increased catalyst dosage and optimal initial RhB concentration were responsible for the enhanced photocatalytic degradation. Quenching tests revealed that the predominant free radicals in the CdS/MIL-(53)-RhBaq-visible light system was O2-rad ; nevertheless, h+ and rad OH also contributed to a certain degree. The enhanced photocatalytic performance was ascribed to the formation of heterojunction structure between CdS and MIL-53(Fe) which significantly suppressed the recombination of photogenerated electron-hole pairs. Moreover, the reusability of 1.5-CdS/MIL composite was also studied.

(3-Methylbenzonitrile-1κN-cis-tetrakis(μ-N-phenylacetamidato-1:2κ4N:O;1:2κ4O:N-dirhodium(II(Rh—Rh

Directory of Open Access Journals (Sweden)

Cassandra T. Eagle

2014-08-01

Full Text Available The complex molecule of the title compound, [Rh2{N(C6H5COCH3}4(NCC7H7], has crystallographically-imposed mirror symmetry. The four acetamide ligands bridging the dirhodium core are arranged in a 2,2-cis manner with two N atoms and two O atoms coordinating to the unique RhII atom cis to one another. The Neq—Rh—Rh—Oeq torsion angles on the acetamide bridge are 0.75 (7 and 1.99 (9°. The axial nitrile ligand completes the distorted octahedral coordination sphere of one RhII atom and shows a nonlinear coordination, with an Rh—N—C bond angle of 162.8 (5°; the N—C bond length is 1.154 (7 Å.

(2aR*,5S*,6aS*,8aS*,E-Ethyl 5-hydroxy-7,7,8a-trimethyl-8-oxo-2,2a,6,6a,7,8,8a,8b-octahydro-1H-pentaleno[1,6-bc]oxepine-4-carboxylate

Directory of Open Access Journals (Sweden)

Goverdhan Mehta

2012-12-01

Full Text Available The title compound, C17H24O5, featuring a 2-carbethoxy-3-oxepanone unit in its intramolecularly O—H...O hydrogen-bonded enol form, was obtained via [(CF3CO22Rh]2-catalysed intramolecular O—H bond insertion in the α-diazo-ω-hydroxy-β-ketoester, ethyl 4-[(1S,3aS,6R,6aS-6-hydroxy-2,2,3a-trimethyl-3-oxo-octahydropentalen-1-yl]-2-diazo-3-oxobutanoate. The seven-membered oxacyclic ring, thus constructed on a cis-fused diquinane platform, was found to adopt a distorted boat–sofa conformation.

Thermal treatment induced transition from Zn3(OH)2(BDC)2 (MOF-69c) to Zn4O(BDC)3 (MOF-5)

CSIR Research Space (South Africa)

Ren, Jianwei

2013-01-01

Full Text Available A simple thermal treatment induced transition from Zn3(OH)2(BDC)2 (MOF-69c) to Zn4O(BDC)3 (MOF-5) is reported. Phase crystallinity, pore characteristics and hydrogen storage capacities of the resulting crystals were investigated. It is shown...

Modulare und durchgängige Produktmodelle als Erfolgsfaktor zur Bedienung einer Omni-Channel-Architektur - PLM 4.0

Science.gov (United States)

Golovatchev, Julius; Felsmann, Marcus

Mit der Transformation der Wertschöpfungsstrukturen von Utility 1.0 zu Utility 4.0 erfolgt offensichtlich auch eine Veränderung des Produkts. Vor dem Hintergrund disruptiver Technologien (IoT, Big Data, Cloud, Robotics etc.) und auch gesellschaftlicher Veränderungen entstehen ständig neue Geschäftsmodelle und Produkte, die über die reine Versorgungsdienstleistung (z. B. Strom) hinausgehen. Dabei muss der wertvolle Rohstoff Produktdaten für smarte Produkte durchgängiger und schneller nutzbar gemacht werden. Die modularen und durchgängigen Produktstrukturen leisten einen Beitrag zur Beherrschung von Komplexität und stellen somit einen wesentlichen Hebel für erfolgreiche Produktentwicklung und -management dar. In diesem Beitrag werden Ansätze beschrieben, wie es den vor der Herausforderung Utility 4.0 stehenden Unternehmen gelingen kann, Smart-Energy-Produkte so zu modellieren, dass sie die Interoperabilität der einzelnen Produktionsmodule sicherstellt und ein Ende-zu-Ende-Management ermöglicht.

Synthesis and sonocatalytic performance of a ternary magnetic MIL-101(Cr)/RGO/ZnFe2O4 nanocomposite for degradation of dye pollutants.

Science.gov (United States)

Nirumand, Ladan; Farhadi, Saeed; Zabardasti, Abedin; Khataee, Alireza

2018-04-01

In this study, new ternary magnetic MIL-101(Cr)/RGO/ZnFe 2 O 4 catalyst (with 30% wt of ZnFe 2 O 4 ) was synthesized via a hydrothermal route for sonodegradation of organic dyes. The structural, optical and magnetic properties of the nanocomposite were detected by means of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), UV-visible spectroscopy (UV-visible), field emission scanning electron microscopy (FESEM), energy dispersive X-ray (EDX) spectroscopy, vibrating sample magnetometer (VSM), atomic force microscopy (AFM), Raman spectroscopy and BET surface area analysis. To evaluate the sonocatalytic activity of the as-prepared MIL-101(Cr)/RGO/ZnFe 2 O 4 nanocomposite, the H 2 O 2 -assisted degradation of organic dyes such as congo red (CR), methylene blue (MB), Rhodamine B (RhB) and methyl orange (MO) in aqueous solution was studied under ultrasound irradiation. The obtained results indicated that the ternary MIL-101(Cr)/RGO/ZnFe 2 O 4 nanocomposite had better performance for sonodegradation of these dyes than MIL-101(Cr)/RGO, pure MIL-101(Cr) or ZnFe 2 O 4 . The enhanced sonocatalytic performance of the as-prepared ternary nanocomposite could be attributed to the fast generation and separation of charge carriers (electrons and holes) in ZnFe 2 O 4 and MIL-101(Cr) and their transfer to the surface of graphene sheets. Moreover, the relatively high specific surface area of the MIL-101(Cr)/rGO and magnetic property of ZnFe 2 O 4 improve the degradation efficiency of the dyes. The recovery of the ternary magnetic sonocatalyst from treated water could be easily achieved using an external magnetic field. The main influence factors on the sonocatalytic activity such as catalyst dosage and dye initial concentration were also investigated. The trapping experiments indicated that OH radicals are the prominent active species in dye degradation. In addition, the reusability test, was also carried out to ensure the stability of the employed sonocatalyst

Synthesis, Crystal and Electronic Structure of the Quaternary Magnetic EuTAl4Si2 (T = Rh and Ir) Compounds

Energy Technology Data Exchange (ETDEWEB)

Maurya, Arvind [Tata Institute of Fundamental Research; Thamizhavel, Arumugam [Tata Institute of Fundamental Research; Provino, Alessia [University of Genova; Pani, Marcella [University of Genova; Manfrinetti, Pietro [University of Genova; Paudyal, Durga [Ames Laboratory; Dhar, Sudesh Kumar [Tata Institute of Fundamental Research

2014-01-22

Single crystals of the quaternary europium compounds EuRhAl4Si2 and EuIrAl4Si2 were synthesized by using the Al–Si binary eutectic as a flux. The structure of the two quaternary compounds has been refined by single crystal X-ray diffraction. Both compounds are stoichiometric and adopt an ordered derivative of the ternary KCu4S3 structure type (tetragonal tP8, P4/mmm). The two compounds reported here represent the first example of a quaternary and truly stoichiometric 1:1:4:2 phase crystallizing with this structure type. In light of our present results, the structure of the BaMg4Si3 compound given in literature as representing a new prototype is actually isotypic with the KCu4S3 structure. Local spin density approximation including the Hubbard U parameter (LSDA + U) calculations show that Eu ions are in the divalent state, with a significant hybridization between the Eu 5d, Rh (Ir) 4d (5d), Si 3p and Al 3p states. Magnetic susceptibility measured along the [001] direction confirms the divalent nature of the Eu ions in EuRhAl4Si2 and EuIrAl4Si2, which order magnetically near 11 and 15 K, respectively.

Thermomagnetic properties of Co1-x Zn x Fe2O4 (x=0.1-0.5) nanoparticles

International Nuclear Information System (INIS)

Arulmurugan, R.; Vaidyanathan, G.; Sendhilnathan, S.; Jeyadevan, B.

2006-01-01

Ultra fine particles of Co 1- x Zn x Fe 2 O 4 with stoichiometric proportion (x) varying from 0.1 to 0.5 were prepared by the usual co-precipitation method. The preparation procedure favored the formation of complex Co-Zn-substituted ferrite nanoparticles. The particles were characterized by XRD. The particle size was calculated by using the Debye-Scherrer formula. The size of the particles precipitated was less than 12 nm. Thermal studies were carried out using simultaneous TG-DTA studies. TG-DTA studies confirmed the presence of associated water content in the precipitated nanoparticles and indicated that ferritization was complete. The temperature-dependent magnetization was recorded at two different fields (5 and 1 kOe). Curie temperature of the powder samples was calculated by extrapolating the linear part of the temperature-dependent magnetization data measured at 1 kOe. Thermomagnetic coefficient which is the first derivative of the temperature-dependent magnetization curve help us in understanding the redistribution of cations between the A and B sites, taking place during the process of heating in the case of nanoparticles. The temperature at which cation redistribution takes place depends on the zinc concentration. From the value of thermomagnetic coefficient and the temperature range, where k T is maximum, it is clear that Co 0.5 Zn 0.5 Fe 2 O 4 particles can be used for the preparation of temperature-sensitive ferrofluid

Half metallic ferromagnetism in tri-layered perovskites Sr{sub 4}T{sub 3}O{sub 10}(T = Co, Rh)

Energy Technology Data Exchange (ETDEWEB)

Ghimire, Madhav Prasad, E-mail: ghimire.mpg@gmail.com [Faculty of Science, Nepal Academy of Science and Technology, P. O. Box 3323, Khumaltar, Lalitpur (Nepal); International Center for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science, Tsukuba 305-0044 (Japan); Thapa, R. K.; Sandeep [Department of Physics, Mizoram University, Aizawl 796-004 (India); Rai, D. P. [Department of Physics, Pachhunga University College, Aizawl 796-001 (India); Sinha, T. P. [Department of Physics, Bose Institute, Kolkata 700-009 (India); Hu, Xiao [International Center for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science, Tsukuba 305-0044 (Japan)

2015-02-14

First-principles density functional theory (DFT) is used to investigate the electronic and magnetic properties of Sr{sub 4}Rh{sub 3}O{sub 10}, a member of the Ruddlesden-Popper series. Based on the DFT calculations taking into account the co-operative effect of Coulomb interaction (U) and spin-orbit couplings (SOC), Sr{sub 4}Rh{sub 3}O{sub 10} is found to be a half metallic ferromagnet (HMF) with total magnetic moment μ{sub tot} = 12 μ{sub B} per unit cell. The material has almost 100% spin-polarization at the Fermi level despite of sizable SOC. Replacement of Rh atom by the isovalent Co atom is considered. Upon full-replacement of Co, a low-spin to intermediate spin transition happens resulting in a HMF state with the total magnetic moment three-time larger (i.e., μ{sub tot} = 36 μ{sub B} per unit cell), compared to Sr{sub 4}Rh{sub 3}O{sub 10}. We propose Sr{sub 4}Rh{sub 3}O{sub 10} and Sr{sub 4}Co{sub 3}O{sub 10} as candidates of half metals.

Unraveling the resistive switching effect in ZnO/0.5Ba(Zr{sub 0.2}Ti{sub 0.8})O{sub 3}-0.5(Ba{sub 0.7}Ca{sub 0.3})TiO{sub 3} heterostructures

Energy Technology Data Exchange (ETDEWEB)

Silva, J.P.B., E-mail: josesilva@fisica.uminho.pt [Centre of Physics, University of Minho, Campus de Gualtar, 4710-057 Braga (Portugal); IFIMUP and IN-Institute of Nanoscience and Nanotechnology, Departamento de Física e Astronomia, Faculdade de Ciências da Universidade do Porto, Rua do Campo Alegre 687, 4169-007 Porto (Portugal); Vorokhta, M.; Dvořák, F. [Department of Surface and Plasma Science, Faculty of Mathematics and Physics, Charles University, V Holešovičkách 2, 18000 Prague 8 (Czech Republic); Sekhar, K.C. [Centre of Physics, University of Minho, Campus de Gualtar, 4710-057 Braga (Portugal); Department of Physics, School of Basic and Applied Science, Central University of Tamil Nadu, Thiruvarur 610 101 (India); Matolín, V. [Department of Surface and Plasma Science, Faculty of Mathematics and Physics, Charles University, V Holešovičkách 2, 18000 Prague 8 (Czech Republic); Moreira, J. Agostinho [IFIMUP and IN-Institute of Nanoscience and Nanotechnology, Departamento de Física e Astronomia, Faculdade de Ciências da Universidade do Porto, Rua do Campo Alegre 687, 4169-007 Porto (Portugal); Pereira, M.; Gomes, M.J.M. [Centre of Physics, University of Minho, Campus de Gualtar, 4710-057 Braga (Portugal)

2017-04-01

Highlights: • ZnO/0.5BZT-0.5BCT heterostructures exhibited resistive switching (RS) ratio ≥ 10 4. • Effect of oxygen pressure used in the deposition of ZnO on RS ratio is highlighted. • Determination of the Band alignment in ZnO/0.5BZT-0.5BCT heterojunctions from XPS. • Resistive Switching is explained based on charge coupling effect. - Abstract: This work reports the effect of partial oxygen pressure, used in the deposition of the ZnO layer, on the band alignment at ZnO – 0.5Ba(Zr{sub 0.2}Ti{sub 0.8})O{sub 3}-0.5(Ba{sub 0.7}Ca{sub 0.3})TiO{sub 3} (0.5BZT-0.5BCT) interface and on the resistive switching (RS) behavior of pulsed laser deposited ZnO/0.5BZT-0.5BCT heterostructures. X-ray photoelectron spectroscopy (XPS) has been employed to measure the valence band offset and the conduction band offset of the ZnO/0.5BZT-0.5BCT heterojunctions. The valence and conduction band offsets of the ZnO/0.5BZT-0.5BCT heterostucture with ZnO deposited at 10{sup −2} mbar of partial oxygen pressure were found to be 0.27 and 0.80 eV, respectively. The RS effect in heterostructures is explained on the base of the charge coupling between the switchable polarization of ferroelectric layer and the non-switchable polarization of semiconductor layer. The heterostructure with ZnO deposited at 10{sup −2} mbar of partial oxygen pressure displays optimum RS characteristics, with a switching ratio ≥ 10{sup 4} and excellent retention and endurance characteristics. The optimum RS characteristics are attributed to a good interface quality with enough carrier concentration in ZnO, as evidenced by XPS.

Einfluß der Stimulation mit CpG-Oligodesoxynukleotiden und Kostimulation mit CpG-Desoxynukleotiden und IL-2 auf Proliferation, Zytokinproduktion und Expression von Oberflächenmolekülen bei B-CLL-Zellen

OpenAIRE

Kronschnabl, Manuela

2005-01-01

B-CLL-Zellen sind langlebige Zellen, die aufgrund einer Apoptoseinhibition akkumulieren. Sie führen zu einer unzureichenden Immunantwort, bedingt durch die geringe Dichte an T-Zell-aktivierenden Oberflächenmolekülen. Durch CpG-ODN (bakterielle DNA) und IL-2 können diese Oberflächenmoleküle bei normalen und malignen B-Zellen hochreguliert sowie Proliferation und Sekretion von Immunglo-bulin und Zytokinen induziert werden. Diese Arbeit untersuchte die Expression der Oberflächenmoleküle CD 25, C...

CXCR5+ CD8+ T Cells Indirectly Offer B Cell Help and Are Inversely Correlated with Viral Load in Chronic Hepatitis B Infection.

Science.gov (United States)

Jiang, Hang; Li, Linhai; Han, Jiang; Sun, Zhiwei; Rong, Yihui; Jin, Yun

2017-04-01

Treatment options for chronic hepatitis B (CHB) infection are extremely limited. CXCR5 + CD8 + T cell is a novel cell subtype and could possess strong cytotoxic properties in HIV infection. In this study, we investigated the role of CXCR5 + CD8 + T cells in CHB patients. Compared to healthy individuals, both CHB patients and hepatitis B virus (HBV)-infected hepatocellular carcinoma patients presented significant upregulation of CXCR5 + CD8 + T cells in peripheral blood, in which CXCR5 + CD8 + T cells were negatively correlated with the frequency of CXCR5 + CD4 + T cells in CHB patients. After PMA+ionomycin stimulation, CXCR5 + CD8 + T cells from CHB patients presented significantly higher transcription level of interferon gamma (IFN-γ), interleukin 10 (IL-10), and IL-21, as well as higher IL-10 and IL-21 protein secretion, than CXCR5 - CD8 + T cells. Unlike CXCR5 + CD4 + T cells, when incubated with naive CD19 + CD27 - B cells, CXCR5 + CD8 + T cells alone did not upregulate IgM, IgG, and IgA secretion. However, addition of CXCR5 + CD8 + T cells in B cell-CXCR5 + CD4 + T cell coculture significantly increased the levels of secreted IgG and IgA, demonstrating that CXCR5 + CD8 + T cell could indirectly offer B cell help. Furthermore, high frequencies of CXCR5 + CD8 + T cells tended to associate with low HBV DNA load, and the frequency of CXCR5 + CD8 + T cells was negatively correlated with alanine aminotransferase (ALT) level. Together, these results suggested that CXCR5 + CD8 + T cells were involved in the antiviral immune responses in CHB and could potentially serve as a therapeutic candidate.

Grain growth kinetics for B2O3-doped ZnO ceramics

Directory of Open Access Journals (Sweden)

Yuksel Berat

2015-06-01

Full Text Available Grain growth kinetics in 0.1 to 2 mol % B2O3-added ZnO ceramics was studied by using a simplified phenomenological grain growth kinetics equation Gn = K0 · t · exp(-Q/RT together with the physical properties of sintered samples. The samples, prepared by conventional ceramics processing techniques, were sintered at temperatures between 1050 to 1250 °C for 1, 2, 3, 5 and 10 hours in air. The kinetic grain growth exponent value (n and the activation energy for the grain growth of the 0.1 mol % B2O3-doped ZnO ceramics were found to be 2.8 and 332 kJ/mol, respectively. By increasing B2O3 content to 1 mol %, the grain growth exponent value (n and the activation energy decreased to 2 and 238 kJ/mol, respectively. The XRD study revealed the presence of a second phase, Zn3B2O6 formed when the B2O3 content was > 1 mol %. The formation of Zn3B2O6 phase gave rise to an increase of the grain growth kinetic exponent and the grain growth activation energy. The kinetic grain growth exponent value (n and the activation energy for the grain growth of the 2 mol % B2O3-doped ZnO ceramics were found to be 3 and 307 kJ/mol, respectively. This can be attributed to the second particle drag (pinning mechanism in the liquid phase sintering.

Enhancement of photocatalytic property on ZnS/MoS2 composite under visible light irradiation

Directory of Open Access Journals (Sweden)

Cheng Jiushan

2017-01-01

Full Text Available In this paper, the composite ZnS/MoS2 was obtained via two steps including solvothermal methods. The as-synthesized sample was characterized by X-ray diffraction (XRD, scanning electron microscopy (SEM and UV-Vis. diffuse reflectance spectra (DRS. The photocatalytic activity of the product was evaluated through photocatalytic degradation of Rhodamine B (Rh B under UV-Vis. light irradiation; the electrical conductivity of ZnS/MoS2 composites was significantly improved compared to ZnS, MoS2, respectively. The results showed that the ZnS/MoS2 composite photocatalyst possesses better photocatalytic activity in degrading Rh B than the single ZnS or the single MoS2. The better photocatalytic properties may be due to the synergetic effect of two semiconductors, because of which electrons and holes were separated effectively. And its specific microstructure played an active role in evaluating photocatalytic performance.

Stellar laboratories. II. New Zn iv and Zn v oscillator strengths and their validation in the hot white dwarfs G191-B2B and RE 0503-289

Science.gov (United States)

Rauch, T.; Werner, K.; Quinet, P.; Kruk, J. W.

2014-04-01

Context. For the spectral analysis of high-resolution and high-signal-to-noise (S/N) spectra of hot stars, state-of-the-art non-local thermodynamic equilibrium (NLTE) model atmospheres are mandatory. These are strongly dependent on the reliability of the atomic data that is used for their calculation. In a recent analysis of the ultraviolet (UV) spectrum of the DA-type white dwarf G191-B2B, 21 Zn iv lines were newly identified. Because of the lack of Zn iv data, transition probabilities of the isoelectronic Ge vi were adapted for a first, coarse determination of the photospheric Zn abundance. Aims: Reliable Zn iv and Zn v oscillator strengths are used to improve the Zn abundance determination and to identify more Zn lines in the spectra of G191-B2B and the DO-type white dwarf RE 0503-289. Methods: We performed new calculations of Zn iv and Zn v oscillator strengths to consider their radiative and collisional bound-bound transitions in detail in our NLTE stellar-atmosphere models for the analysis of the Zn iv - v spectrum exhibited in high-resolution and high-S/N UV observations of G191-B2B and RE 0503-289. Results: In the UV spectrum of G191-B2B, we identify 31 Zn iv and 16 Zn v lines. Most of these are identified for the first time in any star. We can reproduce well almost all of them at log Zn = -5.52 ± 0.2 (mass fraction, about 1.7 times solar). In particular, the Zn iv / Zn v ionization equilibrium, which is a very sensitive Teff indicator, is well reproduced with the previously determined and log g = 7.60 ± 0.05. In the spectrum of RE 0503-289, we identified 128 Zn v lines for the first time and determined log Zn = -3.57 ± 0.2 (155 times solar). Conclusions: Reliable measurements and calculations of atomic data are a pre-requisite for stellar-atmosphere modeling. Observed Zn iv and Zn v line profiles in two white dwarf (G191-B2B and RE 0503-289) ultraviolet spectra were well reproduced with our newly calculated oscillator strengths. This allowed us to

Mechanism of γ-irradiation induced phase transformations in nanocrystalline Mn{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} ceramics

Energy Technology Data Exchange (ETDEWEB)

Jagadeesha Angadi, V. [Department of Physics, Bangalore University, Bangalore, Karnataka 560056 (India); Anupama, A.V.; Choudhary, Harish K.; Kumar, R. [Materials Research Centre, Indian Institute of Science, Bangalore, 560012 (India); Somashekarappa, H.M. [Center for Application of Radioisotopes and Radiation Technology, Mangalore University, Mangalore 574199 (India); Mallappa, M. [Department of Chemistry, Government Science College, Bangalore 560001 (India); Rudraswamy, B. [Department of Physics, Bangalore University, Bangalore, Karnataka 560056 (India); Sahoo, B., E-mail: bsahoo@mrc.iisc.ernet.in [Materials Research Centre, Indian Institute of Science, Bangalore, 560012 (India)

2017-02-15

The structural, infrared absorption and magnetic property transformations in nanocrystalline Mn{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} samples irradiated with different doses (0, 15, 25 and 50 kGy) of γ-irradiation were investigated in this work and a mechanism of phase transformation/decomposition is provided based on the metastable nature of the Mn-atoms in the spinel lattice. The nano-powder sample was prepared by solution combustion route and the pellets of the sample were exposed to γ-radiation. Up to a dose of 25 kGy of γ-radiation, the sample retained the single phase cubic spinel (Fd-3m) structure, but the disorder in the sample increased. On irradiating the sample with 50 kGy γ-radiation, the spinel phase decomposed into new stable phases such as α-Fe{sub 2}O{sub 3} and ZnFe{sub 2}O{sub 4} phases along with amorphous MnO phase, leading to a change in the surface morphology of the sample. Along with the structural transformations the magnetic properties deteriorated due to breakage of the ferrimagnetic order with higher doses of γ-irradiation. Our results are important for the understanding of the stability, durability and performance of the Mn-Zn ferrite based devices used in space applications. - Graphical abstract: The nanocrystalline Mn{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} ceramic sample transforms to crystalline α-Fe{sub 2}O{sub 3} and ZnFe{sub 2}O{sub 4} phases (and amorphous MnO phase) at a γ-irradiation dose of 50 kGy, as MnO goes out of the spinel lattice. The high energy γ-irradiation causes structural damage to the nanomaterials leading to change in morphology of the sample as seen in the SEM images. - Highlights: • Mn atoms are more unstable in the Mn-Zn ferrite spinel lattice than Zn-atoms. • Displacement of Mn atoms by γ-radiation from the lattice renders phase transformation. • In Mn{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4}, Mn-ferrite cell transforms to crystalline α-Fe{sub 2}O{sub 3} and amorphous MnO. • The stable ZnFe{sub 2}O

Effect of Zn/ZSM-5 and FePO4 Catalysts on Cellulose Pyrolysis

Directory of Open Access Journals (Sweden)

Haian Xia

2015-01-01

Full Text Available A series of Zn/ZSM-5 catalysts with different Zn contents and FePO4 were used to pyrolyze cellulose to produce value added chemicals. The nature of these catalysts was characterized by ammonia-temperature programmed desorption (NH3-TPD, IR spectroscopy of pyridine adsorption, and X-ray diffraction (XRD techniques. Noncatalytic and catalytic pyrolytic behaviors of cellulose were studied by thermogravimetric (TG technique. The pyrolytic liquid products, that is, the biooils, were analyzed by gas chromatography-mass spectrometry (GC-MS. The major components of the biooils are anhydrosugars such as levoglucosan (LGA, 1,6-anhydro-β-D-glucofuranose (AGF, levoglucosenone (LGO, 1,6-anhydro-3,4-dideoxy-β-D-pyranosen-2-one, and 1,4:3,6-dianhydro-α-D-glucopyranose (DGP, as well as furan derivatives, alcohols, and so forth. Zn/ZSM-5 samples with Brønsted and Lewis acid sites and the FePO4 catalyst with Lewis acid sites were found to have a significant effect on the pyrolytic behaviors of cellulose and product distribution. These results show that Brønsted and Lewis acid sites modified remarkably components of the biooil, which could promote the production of furan compounds and LGO. On the basis of the findings, a model was proposed to describe the pyrolysis pathways of cellulose catalyzed by the solid acid catalysts.

Cation distribution in Ni-substituted Mn{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} nanoparticles: A Raman, Mössbauer, X-ray diffraction and electron spectroscopy study

Energy Technology Data Exchange (ETDEWEB)

Thota, Suneetha [Microwave Laboratory, Department of Physics, Indian Institute of Technology Delhi, New Delhi 110016 (India); Kashyap, Subhash C., E-mail: skashyap@physics.iitd.ac.in [Microwave Laboratory, Department of Physics, Indian Institute of Technology Delhi, New Delhi 110016 (India); Sharma, Shiv K. [Hawaii Institute of Geophysics and Planetology, University of Hawaii (UH), Honolulu, HI 96822 (United States); Reddy, V.R. [UGC-DAE Consortium for Scientific Research, Khandwa Road, Indore 452017 (India)

2016-04-15

Graphical abstract: - Highlights: • Synthesized Mn{sub 0.5−x}Ni{sub x}Zn{sub 0.5}Fe{sub 2}O{sub 4}, nanoparticles (0.05 ≤ x ≤ 0.45) at low temperature. • Raman studies established that Fe and Zn ions occupy A site in equal fraction. • {sup 57}Fe Mossbauer study revealed that Ni and Mn ions occupy nearly 25% of B sites. • Electron spectroscopy (XPS) confirmed that nearly 25% Fe{sup 3+} dwells at A sites. • Diffraction peak intensity (X-ray) quantified cations distribution at A- and B-sites. - Abstract: In this paper we report the structural, vibration, and electronic-structure parameters (bonding and valence of cations) of single phase cubic mixed spinel nanoparticles of (Zn{sub δ}Mn{sub γ}Fe{sub 1−(γ+δ)})[Ni{sub x}Zn{sub 0.5−δ}Mn{sub 0.5−γ−x}Fe{sub 1+(γ+δ)}]O{sub 4} where x = 0.05–0.45 with an aim to determine cation-distribution i.e. δ and γ in these samples. The Raman spectroscopy has established that only Fe and Zn cations occupy tetrahedral interstitial sites in a FCC anion lattice in nearly equal fraction, and Mössbauer spectra have shown that Fe{sup 3+} cations are present at both, tetrahedral and octahedral interstitial sites and Ni{sup 2+} cations are situated at the octahedral sites in all the substituted samples. The photoelectron spectra also revealed the presence of Fe{sup 3+} cations at both the interstitial sites. The best possible cationic distribution in Ni substituted Mn–Zn ferrites has been estimated by reiteratively calculating the intensity ratios of various pairs of X-ray diffraction peaks and matching with the observed intensity ratios.

Synthesis of nanocrystalline nickel-zinc ferrite (Ni{sub 0.8}Zn{sub 0.2}Fe{sub 2}O{sub 4}) thin films by chemical bath deposition method

Energy Technology Data Exchange (ETDEWEB)

Pawar, D.K. [Department of Chemistry, Shivaji University, Kolhapur 416 004 (M.S.) (India); Pawar, S.M. [Department of Materials Science and Engineering, Chonnam National University, 500 757 (Korea, Republic of); Patil, P.S. [Department of Physics, Shivaji University, Kolhapur 416 004 (M.S.) (India); Kolekar, S.S., E-mail: kolekarss2003@yahoo.co.in [Department of Chemistry, Shivaji University, Kolhapur 416 004 (M.S.) (India)

2011-02-24

Graphical abstract: Display Omitted Research highlights: > We have successfully synthesized nickel-zinc ferrite (Ni{sub 0.8}Zn{sub 0.2}Fe{sub 2}O{sub 4}) thin films on stainless steel substrates using a low temperature chemical bath deposition method. > The surface morphological study showed the compact flakes like morphology. > The as-deposited thin films are hydrophilic (10{sup o} < {theta} < 90{sup o}) whereas the annealed thin films are super hydrophilic ({theta} < 10{sup o}) in nature. > Ni{sub 0.8}Zn{sub 0.2}Fe{sub 2}O{sub 4} thin films could be used in supercapacitor. - Abstract: The nickel-zinc ferrite (Ni{sub 0.8}Zn{sub 0.2}Fe{sub 2}O{sub 4}) thin films have been successfully deposited on stainless steel substrates using a chemical bath deposition method from alkaline bath. The films were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), static water contact angle and cyclic voltammetry measurements. The X-ray diffraction pattern shows that deposited Ni{sub 0.8}Zn{sub 0.2}Fe{sub 2}O{sub 4} thin films were oriented along (3 1 1) plane. The FTIR spectra showed strong absorption peaks around 600 cm{sup -1} which are typical for cubic spinel crystal structure. SEM study revealed compact flakes like morphology having thickness {approx}1.8 {mu}m after air annealing. The annealed films were super hydrophilic in nature having a static water contact angle ({theta}) of 5{sup o}.The electrochemical supercapacitor study of Ni{sub 0.8}Zn{sub 0.2}Fe{sub 2}O{sub 4} thin films has been carried out in 6 M KOH electrolyte. The values of interfacial and specific capacitances obtained were 0.0285 F cm{sup -2} and 19 F g{sup -1}, respectively.

Untersuchungen zur Erdbeerfruchtreifung : Biosynthese von 4-Hydroxy-2,5-dimethyl-3(2H)-furanon und Enzymaktivitäten während des Reifungsprozesses

OpenAIRE

Raab, Thomas

2004-01-01

Die Fruchtreifung stellt einen hochkomplexen Prozess dar, der durch eine Reihe von biochemischen und physiologischen Veränderungen gekennzeichnet ist. Dies umfasst bedeutende Veränderungen von Textur, Farbe sowie die Bildung von geschmacks- und geruchsaktiven Verbindungen. Die vorliegende Arbeit präsentiert neue Erkenntnisse zur Biosynthese von 4-Hydroxy-2,5-dimethyl-3(2H)-furanon (Furaneol®, HDMF), einer Schlüssel-Aromakomponente der Erdbeere (Fragaria x ananassa). Daneben lieferten die durc...

Rhenium (5) and molybdenum (5) complexes with 4',4''(5'')-ditretbutyldibenzo-24-crown-8. Kompleksnye soedineniya reniya (5) i molibdena (5) s 4',4''(5'')-ditretbutildibenzo-24-kraun-8

Energy Technology Data Exchange (ETDEWEB)

Ashurova, N Kh; Yakubov, K G; Basitova, S M; Tashmukhamedova, A K; Sajfullina, N Zh [Tadzhikskij Gosudarstvennyj Univ., Dushanbe (USSR)

1989-10-01

Rhenium and molybdenum complexes in +5 oxidation degree with 4',4''(5'')-ditretbutyldibenzo-24-crown-8 (L) are synthesized with 75-95 % yield. Composition and structure of compounds produced are investigated using element analysis, conductometry, IR spectroscopy, thermogravimetry methods. Oxidation degree of complexer metal is determined. It is ascertained that the compound composition corresponds to the MOLX{sub 3} formula, where M-Re, Mo; X-Cl{sup -}, Br{sup -}.

Impedance spectroscopy study and phase transition in phospho-vanadium mixed oxide LiZnV{sub 0.5}P{sub 0.5}O{sub 4}

Energy Technology Data Exchange (ETDEWEB)

Rahal, A.; Guidara, Kamel; Megdiche, Makram [Sfax Universite, Laboratoire de Caracterisations Spectroscopiques et Optique des Materiaux (LaSCOM), Faculte des Sciences de Sfax, BP 1171, Sfax (Tunisia); Megdiche Borchani, S. [Sfax Universite, Laboratoire de Caracterisations Spectroscopiques et Optique des Materiaux (LaSCOM), Faculte des Sciences de Sfax, BP 1171, Sfax (Tunisia); Institut Superieur D' Informatique et de Multimedia de Sfax (ISIMS), Pole Technologique de Sfax, Sakiet Ezzit, BP 242, Sfax (Tunisia)

2017-08-15

An X-ray crystallographic study has allowed us to identify a powder of the type LiZnV{sub 0.5}P{sub 0.5}O{sub 4}, which contains 50% of vanadium and 50% of phosphor, inside the binary system LiZnVO{sub 4}-LiZnPO{sub 4}. The structure is isotypic with the phenacite like LiZnP0{sub 4}. X-ray diffraction patterns are indexed according to the lattice parameters of the rhombohedral system and the R3 space group. IR spectra show the presence of VO{sub 4} and PO{sub 4} groups in the network of this material. The experimental results indicate that σ{sub AC}(ω) is proportional to (ω{sup n}). The activation energy found from the Arrhenius plot confirms that the conduction processing of the material is not due to simple hopping mechanism. The temperature dependence of frequency exponent n was investigated to understanding the conduction mechanism in LiZnV{sub 0.5}P{sub 0.5}O{sub 4}. The non-overlapping small Polaron tunneling (NSPT) model can explain the temperature dependence of the frequency exponent. A phase transition at T = 623 K has been evidenced by Differential scanning calorimetry (DSC) and subsequently confirmed by the analysis of dielectric and electric properties. (orig.)

Controllable synthesis of Zn{sub 2}TiO{sub 4}-carbon core/shell nanofibers with high photocatalytic performance

Energy Technology Data Exchange (ETDEWEB)

Zhang, Peng [Center for Advanced Optoelectronic Functional Materials Research, and Key Laboratory of UV Light-Emitting Materials and Technology of Ministry of Education, Northeast Normal University, 5268 Renmin Street, Changchun 130024 (China); Shao, Changlu, E-mail: clshao@nenu.edu.cn [Center for Advanced Optoelectronic Functional Materials Research, and Key Laboratory of UV Light-Emitting Materials and Technology of Ministry of Education, Northeast Normal University, 5268 Renmin Street, Changchun 130024 (China); Zhang, Mingyi; Guo, Zengcai; Mu, Jingbo; Zhang, Zhenyi; Zhang, Xin; Liang, Pingping; Liu, Yichun [Center for Advanced Optoelectronic Functional Materials Research, and Key Laboratory of UV Light-Emitting Materials and Technology of Ministry of Education, Northeast Normal University, 5268 Renmin Street, Changchun 130024 (China)

2012-08-30

Graphical abstract: We describe a controllable route to synthesize Zn{sub 2}TiO{sub 4}-carbon core/shell nanofibers with different thickness of carbon layers (from 2 to 8 nm) as high efficiency photocatalysts. Highlights: Black-Right-Pointing-Pointer Synthesis of Zn{sub 2}TiO{sub 4}-carbon nanofibers with different thickness of carbon layers. Black-Right-Pointing-Pointer Zn{sub 2}TiO{sub 4}-carbon NFs showed photocatalytic activity for the degradation of Rhodamine B. Black-Right-Pointing-Pointer Easy photocatalyst separation and reuse. Black-Right-Pointing-Pointer A general way to fabricate other carbon-coated core/shell photocatalysts. - Abstract: Zn{sub 2}TiO{sub 4}-carbon core/shell nanofibers (Zn{sub 2}TiO{sub 4}-C NFs) with different thickness of carbon layers (from 2 to 8 nm) were fabricated by combining the electrospinning technique and hydrothermal method. The results showed that a uniform carbon layer was formed around the electrospun Zn{sub 2}TiO{sub 4} nanofiber (Zn{sub 2}TiO{sub 4} NFs). By adjusting the hydrothermal fabrication parameters, the thickness of carbon layer varied linearly with the concentration of glucose. Furthermore, the core/shell structure formed between Zn{sub 2}TiO{sub 4} and carbon enhanced the charge separation of pure Zn{sub 2}TiO{sub 4} under ultraviolet excitation, as evidenced by photoluminescence spectra. The photocatalytic studies revealed that the Zn{sub 2}TiO{sub 4}-C NFs exhibited enhanced photocatalytic efficiency of photodegradation of Rhodamine B (RB) compared with the pure Zn{sub 2}TiO{sub 4} NFs under ultraviolet excitation, which might be attributed to the high separation efficiency of photogenerated electrons and holes based on the synergistic effect between carbon and Zn{sub 2}TiO{sub 4}. Notably, the Zn{sub 2}TiO{sub 4}-C NFs could be recycled easily by sedimentation without a decrease of the photocatalytic activity.

Vergleichende Analyse der Expression des Glukokortikoid-Rezeptors und der NF-kappaB Untereinheit p50 in Lymphozyten von Patienten mit rheumatoider Arthritis und Gesunden

OpenAIRE

Klüter, Andreas

2003-01-01

Zielstellung: Es wurden die Expression des antiinflammatorisch wirkenden Transkriptionsfaktors Glukokortikoid-Rezeptor (GR) und der Untereinheit p50 des proinflammatorischen Transkriptionsfaktor NF-kappaB in peripheren mononuklearen Blutzellen (PBMC) von Patienten mit rheumatoider Arthritis (RA) untersucht. Methode: Es wurden unbehandelte und mit Glukokortikoiden vorbehandelte RA-Patienten sowie gesunde Probanden verglichen. Die Expressionsanalyse von GR und der NF-kappaB Untereinheit p50 ...

Synchronicity of mononuclear and dinuclear events in homogeneous catalysis. Hydroformylation of cyclopentene using Rh4(CO)12 and HRe(CO)5 as precursors.

Science.gov (United States)

Li, Chuanzhao; Chen, Li; Garland, Marc

2007-10-31

The combined application of two or more metals in homogeneous catalysis can lead to synergistic effects; however, the phenomenological basis for these observations often goes undetermined. The hetero-bimetallic catalytic binuclear elimination reaction, a system involving both mononuclear and dinuclear intermediates, has been repeatedly suggested as a possible mechanism. In the present contribution, the simultaneous application of Rh4(CO)12 and HRe(CO)5 as precursors in the hydroformylation reaction leads to a very strong synergistic rate effect. In situ spectroscopic measurements confirm the presence of both mononuclear and dinuclear intermediates such as RCORh(CO)4 and RhRe(CO)9 in the active system. Moreover, kinetic analysis confirms interconversion of these intermediates as well as their statistical correlation with organic product formation. Specifically, the rate of hydrogen activation by RhRe(CO)9 is exactly equal to the rate of aldehyde formation from binuclear elimination between HRe(CO)5 and RCORh(CO)4 at all reaction conditions studied. Thus the catalytic events involving mononuclear species and those involving dinuclear species are synchronized. In the present experiments, the new topology is orders of magnitude more efficient than the corresponding unicyclic rhodium system.

Mn{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} nanoparticles with high intrinsic loss power for hyperthermia therapy

Energy Technology Data Exchange (ETDEWEB)

Phong, P.T., E-mail: phamthanhphong@tdt.edu.vn [Department for Management of Science and Technology Development, Ton Duc Thang University, Ho Chi Minh City (Viet Nam); Faculty of Applied Sciences, Ton Duc Thang University, Ho Chi Minh City (Viet Nam); Nam, P.H., E-mail: namph.ims@gmail.com [Institute of Materials Science, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Cau Giay District, Ha Noi City (Viet Nam); Manh, D.H. [Institute of Materials Science, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet Road, Cau Giay District, Ha Noi City (Viet Nam); Lee, In-Ja, E-mail: lij@dongguk.ac.kr [Department of Advanced Materials Chemistry, Dongguk University-Gyeongju, Dongdae-ro 123, Gyeongju-Si, Gyeongbuk 38066 (Korea, Republic of)

2017-07-01

Highlights: • Mn{sub 0.5}Zn{sub 0.5}FeO{sub 4} nanoparticles were synthesized using a hydrothermal method. • The coercivity at different temperatures was studied using the mixed coercivity model. • A superspin glass from strong interactions. • High intrinsic loss power was found to be comparable to that of ferrite and some commercial ferrofluids. - Abstract: Nanosized mixed ferrite Mn{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} with crystalline size ∼15 nm has been prepared by hydrothermal route. XRD patterns confirm that the crystallites have single phase cubic spinel structure. The dynamic scaling analysis on the frequency dependence of spin glass-like transition temperature well explains the model of a transition at finite temperature. The analysis gives critical exponent and parameters as: zν = 10.48, T{sub 0} = 190 K, f{sub 0} = 5.38 × 10{sup 10} and this confirms the occurrence of spin glass-like transition in Mn{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} particles. The saturation magnetization and the coercivity change with temperature. The effective magnetic anisotropy constant of sample was calculated using the law of approach to saturation. The coercivity at different temperatures was deduced using the mixed coercivity model. The calculated coercivity results are in a good agreement with the experimental ones. The magnetic heating ability of Mn{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} magnetic fluid was studied with an induction heating system. The calculated intrinsic loss power (ILP) was 3.75 g nHm{sup 2}/kg. This study indicates that the resulting Mn{sub 0.5}Zn{sub 0.5}Fe{sub 2}O{sub 4} nanoparticles are promising materials in magnetic hyperthermia.

Sorption reactions in groundwater: various aspects to modelling the transport behaviour of zinc; Sorptionsreaktionen im Grundwasser: Unterschiedliche Aspekte bei der Modellierung des Transportverhaltens von Zink

Energy Technology Data Exchange (ETDEWEB)

Hadeler, A.

1999-08-01

The dispersal of trace substance in groundwater may be limited by dissolution and precipitation and, of particular interest in this paper, by sorption and desorption processes. These surface-active processes, which have a decisive influence on groundwater quality, depend on the concomitant geochemical conditions prevailing in the water, the constituents of the aquifer and on the surface properties of the solids. Taking the geochemical conditions prevailing naturally in brown coal mining areas as a point of departure this study was aimed at examining the influence of acidification processes on the transport behaviour inorganic pollutants for the example of zinc. For this purpose oxic column trials were carried out on sandy aquifer material. The data were supplemented by a detailed characterisation of the solid surfaces and modelled on the basis of a transport-reaction model as well as mechanistically with due regard to surface complexing. [German] Die Ausbreitung von Spurenstoffen im Grundwasser wird ausser durch Loesungs- und Faellungsprozesse vor allem durch Sorptions- bzw. Desorptionsvorgaenge limitiert. Diese fuer die Grundwasserqualitaet entscheidenden oberflaechenaktiven Prozesse sind von den variablen geochemischen Randbedingungen im Wasser, vom Stoffbestand des Aquifers und von den Oberflaecheneigenschaften der Feststoffe abhaengig. In Anlehnung an die natuerlichen im Bereich von Braunkohle-Abbaugebieten herrschenden geochemischen Bedingungen wurde der Einfluss von Versauerungsprozessen auf das Transportverhalten von anorganischen Schadstoffen, am Beispiel von Zink, auf der Basis von oxischen Saeulenversuchen an sandigem Aquifermaterial untersucht. Die Daten wurden durch eine detaillierte Charakterisierung der Feststoff-Oberflaechen ergaenzt und sowohl mit Hilfe eines Transport-Reaktionsmodells als auch mechanistisch unter Einbeziehung der Oberflaechenkomplexierung modelliert. (orig.)

Comparative effect of ZnO NPs, ZnO bulk and ZnSO4 in the antioxidant defences of two plant species growing in two agricultural soils under greenhouse conditions.

Science.gov (United States)

García-Gómez, Concepción; Obrador, Ana; González, Demetrio; Babín, Mar; Fernández, María Dolores

2017-07-01

The present study has investigated the toxicity of ZnO NPs to bean (Phaseolus vulgaris) and tomato (Solanum lycopersicon) crops grown to maturity under greenhouse conditions using an acidic (soil pH5.4) and a calcareous soil (soil pH8.3). The potentially available Zn in the soils and the Zn accumulation in the leaves from NPs applied to the soil (3, 20 and 225mgZnkg -1 ) and changes in the chlorophylls, carotenoids and oxidative stress biomarkers were measured at 15, 30, 60 and 90days and compared with those caused by bulk ZnO and ZnSO 4 . The available Zn in the soil and the leaf Zn content did not differ among the Zn chemical species, except in the acidic soil at the highest concentration of Zn applied as Zn ions, where the highest values of the two variables were found. The ZnO NPs showed comparable Zn toxicity or biostimulation to their bulk counterparts and Zn salts, irrespective of certain significant differences suggesting a higher activity of the Zn ion. The treatments altered the photosynthetic pigment concentration and induced oxidative stress in plants. ROS formation was observed at Zn plant concentrations ranging from 590 to 760mgkg -1 , but the effects on the rest of the parameters were highly dependent on the plant species, exposure time and especially soil type. In general, the effects were higher in the acidic soil than in the calcareous soil for the bean and the opposite for the tomato. The similar uptakes and toxicities of the different Zn forms suggest that the Zn ions derived from the ZnO NPs exerted a preferential toxicity in plants. However, several results obtained in soils treated with NPs at 3mgZnkg -1 soil indicated that may exist other underlying mechanisms related to the intrinsic nanoparticle properties, especially at low NP concentrations. Copyright © 2017 Elsevier B.V. All rights reserved.

The John Zink Hamworthy combustion handbook, v.1 fundamentals

CERN Document Server

Baukal, Charles E

2012-01-01

Despite the length of time it has been around, its importance, and vast amounts of research, combustion is still far from being completely understood. Environmental, cost, and fuel consumption issues add further complexity, particularly in the process and power generation industries. Dedicated to advancing the art and science of industrial combustion, The John Zink Hamworthy Combustion Handbook, Second Edition: Volume One - Fundamentals gives you a strong understanding of the basic concepts and theory. Under the leadership of Charles E. Baukal, Jr., top combustion engineers and technologists f

Effect of Si, Mn, Sn on Tensile and Corrosion Properties of Mg-4Zn-0.5Ca Alloys for Biodegradable Implant Materials

Energy Technology Data Exchange (ETDEWEB)

Cho, Dae Hyun; Nam, Ji Hoon; Lee, Byeong Woo; Park, Ji Yong; Shin, Hyun Jung; Park, Ik Min [Pusan National University, Busan (Korea, Republic of)

2015-03-15

Effect of elements Si, Mn, Sn on tensile and corrosion properties of Mg-4Zn-0.5Ca alloys were investigated. The results of tensile properties show that the yield strength, ultimate tensile strength and elongation of Mg-4Zn-0.5Ca alloy increased significantly with the addition of 0.6 wt% Mn. This is considered the grain refinement effect due to addition of Mn. However addition of 0.6 wt% Si decreased yield strength, ultimate tensile strength and elongation. The bio-corrosion behavior of Mg-4Zn-0.5Ca-X alloys were investigated using immersion tests and potentiodynamic polarization test in Hank's solution. Immersion test showed that corrosion rate of Mg-4Zn-0.5Ca-0.6Mn alloy was the lowest rate and addition of 1.0 wt% Sn accelerated corrosion rate due to micro-galvanic effect in α-Mg/CaMgSn phases interface. And corrosion potential (E{sub c}orr) of Mg-4Zn-0.5Ca-0.6Mn alloy was the most noble among Mg-4Zn-0.5Ca-X alloys.

Expression of Aurora-B and FOXM1 predict poor survival in patients with nasopharyngeal carcinoma

Energy Technology Data Exchange (ETDEWEB)

Huang, Pei-Yu; Luo, Dong-Hua; Mai, Hai-Qiang [State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou (China); Sun Yat-sen University Cancer Center, Department of Nasopharyngeal Carcinoma, Guangzhou (China); Li, Yan; Zeng, Ting-Ting; Li, Meng-Qing [State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou (China); Hou, Xue; Zhang, Li [State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou (China); Sun Yat-sen University Cancer Center, Department of Medical Oncology, Guangzhou (China)

2015-08-15

The purpose of this work was to investigate the relationship between Aurora-B, FOXM1, and clinical outcomes in patients with nasopharyngeal carcinoma (NPC) who were treated with a combination of induction chemotherapy and radiotherapy. The expression of Aurora-B and FOXM1 were investigated by immunohistochemistry using a tissue microarray (TMA) containing samples from 166 NPC patients who were treated with cisplatin (DDP) + fluorouracil (5-FU) induction chemotherapy and radiotherapy between 1999 and 2005. The relationship of Aurora-B, FOXM1, and survival of these NPC patients was analyzed. Informative TMA results were obtained in 91 tumor cases for Aurora-B and 93 tumor cases for FOXM1. The 8-year failure-free survival rate (FFS) for the Aurora-B-negative and Aurora-B-positive group was 65.6 and 37.3 %, respectively (p = 0.024), and the 8-year distant FFS (D-FFS) rate was 65.6 and 41.5 %, respectively (p = 0.047). The 8-year overall survival (OS) in the FOXM1-negative group was moderately higher than in the FOXM1-positive group (58.4 vs 39.1 %, p = 0.081). Cox regression analysis revealed that for FFS, Aurora-B expression was a significant prognostic factor (p = 0.025), while for D-FFS, Aurora-B expression was a marginally significant prognostic factor (p = 0.056). When FOXM1 expression was analyzed, the Cox regression analyses showed that FOXM1 expression was a marginally significant prognostic factor (p = 0.056) for OS. Correlation analysis showed that Aurora-B and FOXM1 expression had no significant correlation. Aurora-B and FOXM1 were both adverse prognostic markers for NPC patients treated with chemoradiotherapy. However, the two markers had no significant correlation. (orig.) [German] Ziel war die Untersuchung der Beziehung zwischen Aurora-B, FOXM1 und den klinischen Ergebnissen bei Patienten mit nasopharyngealem Karzinom (NPC), die mit einer Kombinationstherapie aus Induktionschemotherapie und Radiotherapie behandelt wurden. Die Expression von Aurora-B und

Microstructural analysis nanoferritas Mn{sub 0,5}Zn{sub 0,5}Fe{sub 2}O{sub 4} e Mn{sub 0,65}Zn{sub 0,35}Fe{sub 2}O{sub 4} synthesized by combustion reaction; Analise microestrutural de nanoferritas Mn{sub 0,5}Zn{sub 0,5}Fe{sub 2}O{sub 4} e Mn{sub 0,65}Zn{sub 0,35}Fe{sub 2}O{sub 4} sintetizadas por reacao de combustao

Energy Technology Data Exchange (ETDEWEB)

Diniz, V.C.S.; Figueiredo, A.R.; Costa Junior, A.D.S.; Diniz, H.M.; Vieira, D.A.; Costa, A.C.F.M., E-mail: veronicacristhina@hotmail.com [Universidade Federal de Campina Grande (UFCG), PB (Brazil). Departamento de Engenharia de Materiais

2014-07-01

The MnZn ferrites are ferrimagnetic materials that have been studied and used in various technological fields. In this work investigated the microstructural characteristics of ferrites and Mn{sub 0,5}Zn{sub 0,5}Fe{sub 2}O{sub 4} Mn{sub 0,65}Zn{sub 0,35}Fe{sub 2}O{sub 4} synthesized by combustion reaction in 200g scale production. The samples were characterized by XRD, crystallinity, crystallite size, X-ray fluorescence and scanning electron microscopy. Given the results it was observed that for both samples the synthesis combustion reaction was efficient for the production of single-phase ferrites with high crystallinity. With respect to the analysis of X-ray fluorescence was noted that the experimental values composition were consistent with the theoretical values calculated for both samples. Regarding morphology for both samples, the formation of the porous powders with feature consisting of dense clumps in the form of irregular foam was observed. (author)

Toxische effecten van zink op de worm Eisenia andrei; resultaten proefveldexperimenten Amsterdam 1995 en 1996

NARCIS (Netherlands)

Bakker J; Posthuma L; Baerselman R; ECO/EEB

1997-01-01

De toxische effecten van zink voor de compostworm Eisenia andrei werden bestudeerd in twee proefveldexperimenten, om de veldrelevantie van laboratorium-toxiciteitsgegevens te onderzoeken indien blootstellingscondities op natuurlijke wijze fluctueren. Coconproductie werd hierbij gebruikt als

Periodontal wound healing/regeneration following the application of rhGDF-5 in a beta-TCP/PLGA carrier in critical-size supra-alveolar periodontal defects in dogs.

Science.gov (United States)

Kwon, David H; Bisch, Frederick C; Herold, Robert W; Pompe, Cornelius; Bastone, Patrizia; Rodriguez, Nancy A; Susin, Cristiano; Wikesjö, Ulf M E

2010-07-01

The objective of this study was to evaluate the effect of a novel recombinant human GDF-5 (rhGDF-5) construct intended for onlay and inlay indications on periodontal wound healing/regeneration. Contralateral, surgically created, critical-size, 6-mm, supra-alveolar periodontal defects in five adult Hound Labrador mongrel dogs received rhGDF-5 coated onto beta-tricalcium phosphate (beta-TCP) particles and immersed in a bioresorbable poly(lactic-co-glycolic acid) (PLGA) composite or the beta-TCP/PLGA carrier alone (control). The rhGDF-5 and control constructs were moulded around the teeth and allowed to set. The gingival flaps were then advanced; flap margins were adapted 3-4 mm coronal to the teeth and sutured. The animals were euthanized at 8 weeks post-surgery when block biopsies were collected for histometric analysis. Healing was generally uneventful. A few sites exhibited minor exposures. Three control sites and one rhGDF-5 site (in separate animals) experienced more extensive wound dehiscencies. The rhGDF-5 and control constructs were easy to apply and exhibited adequate structural integrity to support the mucoperiosteal flaps in this challenging onlay model. Limited residual beta-TCP particles were observed at 8 weeks for both rhGDF-5/beta-TCP/PLGA and beta-TCP/PLGA control sites. The rhGDF-5/beta-TCP/PLGA sites showed significantly greater cementum (2.34 +/- 0.44 versus 1.13 +/- 0.25 mm, p=0.02) and bone (2.92 +/- 0.66 versus 1.21 +/- 0.30 mm, p=0.02) formation compared with the carrier control. Limited ankylosis was observed in four of five rhGDF-5/beta-TCP/PLGA sites but not in control sites. Within the limitations of this study, the results suggest that rhGDF-5 is a promising candidate technology in support of periodontal wound healing/regeneration. Carrier and rhGDF-5 dose optimization are necessary before further advancement of the technology towards clinical evaluation.

Solvothermal Synthesis of Zn2SnO4 Nanocrystals and Their Photocatalytic Properties

Directory of Open Access Journals (Sweden)

Guang Sun

2014-01-01

Full Text Available Crystalline Zn2SnO4 nanoparticles were successfully synthesized via a simple solvothermal route by using Zn(CH3COO2·2H2O and SnCl4·5H2O as source materials, NaOH as mineralizing agent, and water and ethanol as mixed solvents. The used amount of NaOH was found to have an important influence on the formation of Zn2SnO4. When the molar ratio of OH− : Zn2+ : Sn4+ was set in the range from 4 : 2 : 1 to 8 : 2 : 1, Zn2SnO4 nanoparticles with different shape and size were obtained. However, when the molar ratio of OH− : Zn2+ : Sn4+ was set as 10 : 2 : 1, a mixture phase of ZnO and ZnSn(OH6 instead of Zn2SnO4 was obtained. Photodegradation measurements indicated that the Zn2SnO4 nanoparticles own better photocatalytic property to depredate methyl orange than the Zn2SnO4 nanopolyhedrons. The superior photocatalytic properties of Zn2SnO4 nanoparticles may be contributed to their small crystal size and high surface area.

DEWEK '98: 4. German wind power conference; DEWEK '98: 4. Deutsche Windenergie-Konferenz. Tagungsband

Energy Technology Data Exchange (ETDEWEB)

Gerdes, B [ed.

1999-07-01

The conference report comprises 90 papers and posters on the following subjects: 1. Technological developments (e.g. use of adaptive structures systems, active stalle wind power systems, systems for early detection of errors); 2. Design and optimisation; 3. Wind forecasts; 4. Operation analyses (e.g. active and passive stall, collective loads, wind power systems in cold climates); 5. Wind power systems and the environment; 6. Offshore wind power generation; 7. Electric characteristics (e.g. modelling of flicker, energy conditioning in distribution systems with a high wind power share); 8. Economic efficiency (e.g. economic efficiency of offshore wind parks on the North Sea coast); 9. Network quality; 10. Rotor development (e.g. noise reduction); 11. Certification and methods of measurement. [German] Der Tagungsband enhaelt 90 Fach- und Posterbeitraege, die sich mit den folgenden Schwerpunkten befassen: 1. Technologische Entwicklungen (z.B. Einsatz von adaptiven Struktursystemen; Active-Stall-WKA; Fehlerfrueherkennungssystemen). 2. Auslegung und Optimierung. 3. Windprognosen. 4. Betriebsanalysen (z.B. Aktive Stall/Passive Stall im Vergleich; Lastkollektive von WKA; WKA in kaltem Klima). 5. Windenergieanlagen und Umwelt. 6. Offshore-Windenergienutzung. 7. Elektrische Eigenschaften (z.B. Modellierung des 'Flickerverhaltens' von WKA; Energiekonditionierung in Verteilnetzen mit hohem Windenergieanteil). 8. Wirtschaftlichkeit (z.B. Wirtschaftlichkeit von Offshore-Windparks der Norddeutschen Kuestenlinie). 9. Netzqualitaet. 10. Rotorentwicklung (z.B. Reduzierung der Schallabstrahlung von WKAs). 11. Zertifizierung von Messmethoden. (AKF)

Analogues of amphibian alkaloids: total synthesis of (5R,8S,8aS-(--8-methyl-5-pentyloctahydroindolizine (8-epi-indolizidine 209B and [(1S,4R,9aS-(--4-pentyloctahydro-2H-quinolizin-1-yl]methanol

Directory of Open Access Journals (Sweden)

de Koning Charles B

2008-01-01

Full Text Available Abstract Background Prior work from these laboratories has centred on the development of enaminones as versatile intermediates for the synthesis of alkaloids and other nitrogen-containing heterocycles. In this paper we describe the enantioselective synthesis of indolizidine and quinolizidine analogues of bicyclic amphibian alkaloids via pyrrolidinylidene- and piperidinylidene-containing enaminones. Results Our previously reported synthesis of racemic 8-epi-indolizidine 209B has been extended to the laevorotatory enantiomer, (--9. Attempts to adapt the synthetic route in order to obtain quinolizidine analogues revealed that a key piperidinylidene-containing enaminone intermediate (+-28 was less tractable than its pyrrolidinylidene counterpart, thereby necessitating modifications that included timing changes and additional protection-deprotection steps. A successful synthesis of [(1S,4R,9aS-4-pentyloctahydro-2H-quinolizin-1-yl]methanol (--41 from the chiral amine tert-butyl (3R-3-{benzyl [(1R-1-phenylethyl]amino}octanoate (+-14 was achieved in 14 steps and an overall yield of 20.4%. Conclusion The methodology reported in this article was successfully applied to the enantioselective synthesis of the title compounds. It paves the way for the total synthesis of a range of cis-5,8-disubstituted indolizidines and cis-1,4-disubstituted quinolizidines, as well as the naturally occurring trans-disubstituted alkaloids.

Crossrelaxations and non-radiative energy transfer from (4G5/2) Sm3+ → (5D0) Eu3+: B2O3–ZnO glasses

International Nuclear Information System (INIS)

Naresh, V.; Rudramadevi, B.H.; Buddhudu, S.

2015-01-01

Graphical abstract: The energy transfer process occurring from Sm 3+ to Eu 3+ in B 2 O 3 –ZnO (BZn) glasses is analyzed. Based on the Foster–Dexter theory, the possibility of energy transfer between Sm 3+ and Eu 3+ has been demonstrated from the spectral overlap of Eu 3+ absorption and Sm 3+ emission, photoluminescence spectra, energy level diagram and lifetime measurements. The energy transfer mechanism in (Sm 3+ + Eu 3+ ) co-doped glass is governed by dipole–dipole interaction. - Highlights: • Spectroscopic properties of individually doped Sm 3+ , Eu 3+ & co-doped (Sm 3+ + Eu 3+ ) in BZn glasses were studied separately. • The effect of Eu 3+ concentration on luminescence properties is explained from cross-relaxations. • Energy transfer from Sm 3+ ( 4 G 5/2 ) to Eu 3+ ( 5 D 0 ) has been explained from Foster–Dexter theory. • Dipole–dipole mechanism governs the energy transfer from Sm 3+ to Eu 3+ . - Abstract: The present paper reports on the results concerning to photoluminescence features of Eu 3+ , Sm 3+ ions and energy transfer process occurring from Sm 3+ to Eu 3+ doped in 45 B 2 O 3 –55 ZnO (BZn) glasses prepared by melt quenching technique. Luminescence quenching as a function of Eu 3+ concentration in BZn glasses has been discussed. Among the studied concentrations, 0.5 mol% of Eu 3+ is optimized because it has exhibited red emission transition 5 D 0 → 7 F 2 . With regard to Sm 3+ glasses, orange emission at 602 nm ( 4 G 5/2 → 6 H 7/2 ) has been noticed on exciting with λ exci = 403 nm. Based on the Foster–Dexter theory, the possibility of energy transfer between Sm 3+ and Eu 3+ has been explained from the spectral overlap of Eu 3+ absorption and Sm 3+ emission. The optimized concentration 0.5 mol% of Eu 3+ is co-doped with Sm 3+ in various concentrations ranging from 0.1 to 1.5 mol% inorder to study the sensitization effect of Sm 3+ on Eu 3+ luminescence. The results have revealed that with the addition of Sm 3+ to Eu 3+ : BZn

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

Heteroleptic complexes of Zn(II) based on 1-(5-bromo-2-hydroxybenzylidene)-4-phenylthiosemicarbazide: Synthesis, structural characterization, theoretical studies and antibacterial activity

Science.gov (United States)

Azarkish, Mohammad; Akbari, Alireza; Sedaghat, Tahereh; Simpson, Jim

2017-04-01

Four new ternary complexes, [ZnL (2,2‧-bipy)] (1), Zn2L2(4,4‧-bipy)] (2), [ZnL(Imd)]·H2O (3) and [ZnL3(MeImd)] (4), have been synthesized from the reaction of Zn(II) acetate with 1-(5-bromo-2-hydroxybenzylidene)-4-phenylthiosemicarbazide (H2L) in the presence of a heterocyclic base, 2,2‧-bipyridine, 4,4‧-bipyridine, imidazole or 2-methylimidazole, as an auxiliary ligand. The complexes have been investigated by elemental analysis and FT-IR, UV-Vis and 1HNMR spectroscopy. These data show that the thiosemicarbazone acts as a tridentate dianionic ligand and coordinates via the thiol group, imine nitrogen, and phenolic oxygen. The coordination sphere was completed by the nitrogen atom(s) of the secondary ligand. The structure of 1 was also confirmed by X-ray crystallography and shown to be a five coordinate complex with coordination geometry between the square-pyramidal and trigonal-bipyramidal. Density functional theory (DFT) calculations including geometry optimization, vibrational frequencies and electronic absorptions have been performed for 1 with the B3LYP functional at the TZP(6-311G*) basis set using the Gaussian 03 or ADF 2009 packages. The optimization calculation showed that the crystallographically determined geometry parameters can be reproduced with that basis set. Experimental IR frequencies and calculated vibration frequencies also support each other. The in vitro antibacterial activities of the ligand and complexes have been evaluated against Gram-positive (B. subtilis and S. aureus) and Gram-negative (P. aeruginosa) bacteria and compared with the standard antibacterial drugs. The results reveal that all of the complexes show much better activity in comparison to the individual thiosemoicarbazone ligand (H2L), against all bacterial strains used, with complex 3 showing the most promising results.

2-tert-Butyl-5,6,7,8,9,10-hexahydrocyclohepta[b]indole

Directory of Open Access Journals (Sweden)

Janina Wobbe

2011-09-01

Full Text Available 2-tert-Butyl-5,6,7,8,9,10-hexahydrocyclohepta[b]indole was synthesized by reaction of cycloheptanone and (4-tert-butylphenylhydrazine hydrochloride in the presence of sodium acetate and sulfuric acid in glacial acetic acid via Fischer indole synthesis.

Enhancing blockade of Plasmodium falciparum erythrocyte invasion: assessing combinations of antibodies against PfRH5 and other merozoite antigens.

Directory of Open Access Journals (Sweden)

Andrew R Williams

Full Text Available No vaccine has yet proven effective against the blood-stages of Plasmodium falciparum, which cause the symptoms and severe manifestations of malaria. We recently found that PfRH5, a P. falciparum-specific protein expressed in merozoites, is efficiently targeted by broadly-neutralizing, vaccine-induced antibodies. Here we show that antibodies against PfRH5 efficiently inhibit the in vitro growth of short-term-adapted parasite isolates from Cambodia, and that the EC(50 values of antigen-specific antibodies against PfRH5 are lower than those against PfAMA1. Since antibody responses elicited by multiple antigens are speculated to improve the efficacy of blood-stage vaccines, we conducted detailed assessments of parasite growth inhibition by antibodies against PfRH5 in combination with antibodies against seven other merozoite antigens. We found that antibodies against PfRH5 act synergistically with antibodies against certain other merozoite antigens, most notably with antibodies against other erythrocyte-binding antigens such as PfRH4, to inhibit the growth of a homologous P. falciparum clone. A combination of antibodies against PfRH4 and basigin, the erythrocyte receptor for PfRH5, also potently inhibited parasite growth. This methodology provides the first quantitative evidence that polyclonal vaccine-induced antibodies can act synergistically against P. falciparum antigens and should help to guide the rational development of future multi-antigen vaccines.

Total emissivity and spectral emissivity of high-temperature materials; Gesamtemissionsgrad und spektraler Emissionsgrad von Hochtemperaturmaterialien

Energy Technology Data Exchange (ETDEWEB)

Neuer, G.; Pohlmann, P.; Schreiber, E.

1998-05-01

A new emissivity measurement device with inductive sample heating is described. The disc shaped samples can be measured between 800 C and 2000 C in vacuum or in each available gas atmosphere. Two kinds of surface temperature measurement methods are described, one by measuring in a blackbody hole and one by measuring at the surface without additional measures to correct emissivity. Total normal and spectral emissivity at wavelengths between 0,5 {mu}m and 8,3 {mu}m of various high temperature materials like platinum and Pt-Rh-alloys, siliconcarbide and molybdenum disilicide have been measured. From the investigated materials a few have been selected as reference samples for comparative emissivity measurements fullfilling the requirement of stability on air up to 400 C to 1000 C in order to ensure reproducibility of the results at different measurement conditions in air and in vacuum. (orig.) [Deutsch] Der Aufbau einer neuen Messapparatur fuer Emissionsgradmessungen bei Temperaturen zwischen 1000 C und 2000 C wird beschrieben. Die scheibenfoermigen Proben werden induktiv beheizt, und die Messungen koennen entweder in Vakuum oder einer beliebigen Gasatmosphaere durchgefuehrt werden. Es werden zwei verschiedene Verfahren zur Bestimmung der Oberflaechentemperatur bechrieben, wobei entweder in einer oder direkt an der Oberflaeche ohne zusaetzliche Massnahmen zur Emissionsgradkorrektur gemessen wird. An verschiedenen Hochtemperaturwerkstoffen wie Platin und Platin-Rhodium-Legierungen, Siliziumkarbid mit unterschiedlichen Herstellungsarten und Molybdaen-Disilizid wurden der Gesamtemissionsgrad und der spektrale Emissionsgrad bei Wellenlaengen von 0,5 {mu}m bis 8,3 {mu}m senkrecht zur Oberflaeche gemessen. Aus den untersuchten Materialien wurden solche als Referenzmaterialien fuer vergleichende Emissionsgradmessungen ausgewaehlt, die sowohl im Vakuum als auch in Luft und bei Temperaturen von 1400 C bis 1600 C unter verschiedenen Messbedingungen reproduzierbare Ergebnisse

Cyberbullying und Empathie : affektive, kognitive und medienbasierte Empathie im Kontext von Cyberbullying im Kindes- und Jugendalter

OpenAIRE

Pfetsch, Jan; Müller, Christin R.; Ittel, Angela

2014-01-01

"Bei medial vermittelter Kommunikation sinkt sowohl die Hemmschwelle für aggressive Verhaltensweisen wie Cyberbullying als auch die Wahrscheinlichkeit empathischer Reaktionen. Im Fokus der vorliegenden Studie mit 979 Schülerinnen und Schülern der 4.-8. Klassen (M=12.01, SD=1.68 Jahre, 55% weiblich) stand die Frage, ob Cyberbullies geringere Ausprägungen für affektive, kognitive und medienbasierte Empathie aufweisen als Unbeteiligte. Empathie wurde im Selbst- und Peerbericht erhoben. Hypothese...

Environmental application of millimetre-scale sponge iron (s-Fe{sup 0}) particles (IV): New insights into visible light photo-Fenton-like process with optimum dosage of H{sub 2}O{sub 2} and RhB photosensitizers

Energy Technology Data Exchange (ETDEWEB)

Ju, Yongming, E-mail: juyongming@scies.org [South China Institute of Environmental Sciences, Ministry of Environmental Protection (MEP), Guangzhou 510655 (China); Innovative Laboratory for Environmental Functional Materials and Environmental Applications of Microwave Irradiation, South China Subcenter of State Environmental Dioxin Monitoring Center, Guangzhou 510655 (China); Guangdong Key Laboratory of Agro-Environment Integrated Control, South China Institute of Environmental Sciences, Guangzhou 510655 (China); Yu, Yunjiang, E-mail: yuyunjiang@scies.org [South China Institute of Environmental Sciences, Ministry of Environmental Protection (MEP), Guangzhou 510655 (China); Wang, Xiaoyan; Xiang, Mingdeng; Li, Liangzhong [South China Institute of Environmental Sciences, Ministry of Environmental Protection (MEP), Guangzhou 510655 (China); Deng, Dongyang [South China Institute of Environmental Sciences, Ministry of Environmental Protection (MEP), Guangzhou 510655 (China); Innovative Laboratory for Environmental Functional Materials and Environmental Applications of Microwave Irradiation, South China Subcenter of State Environmental Dioxin Monitoring Center, Guangzhou 510655 (China); Guangdong Key Laboratory of Agro-Environment Integrated Control, South China Institute of Environmental Sciences, Guangzhou 510655 (China); Dionysiou, Dionysios D., E-mail: dionysios.d.dionysiou@uc.edu [Environmental Engineering and Science Program, Department of Biomedical, Chemical and Environmental Engineering (DBCEE), University of Cincinnati, Cincinnati, Ohio, 45221-0012 (United States)

2017-02-05

Highlights: • Synergistic action of Rhodamine B (RhB), visible light, H{sub 2}O{sub 2} and s-Fe{sup 0} is essential. • The complexes of RhB and Fe{sup 3+} eject one electron via ligand-to-metal charge-transfer. • RhB assists the photo-Fenton-like removal of tetrabromobisphenol A (TBBPA). - Abstract: In this study, we firstly develop the photo-Fenton-like system with millimetric sponge iron (s-Fe{sup 0}), H{sub 2}O{sub 2}, visible light (vis, λ ≥ 420 nm) and rhodamine B (RhB), and present a comprehensive study concerning the mechanism. Thus, we investigate (1) the adsorption of RhB onto s-Fe{sup 0}, (2) the photo-Fenton-like removal of RhB over iron oxides generated from the corrosion of s-Fe{sup 0}, (3) the homogeneous photo-Fenton removal of RhB over Fe{sup 2+} or Fe{sup 3+}, (4) the Fe{sup 3+}-RhB complexes, and (5) the photo-Fenton-like removal of tetrabromobisphenol A (TBBPA). The results show that neither the adsorption process over s-Fe{sup 0} nor the photo-Fenton-like process over FeOOH, Fe{sub 3}O{sub 4} and Fe{sub 2}O{sub 3}, achieved efficient removal of RhB. For comparison, in homogeneous photo-Fenton process, the presence of Fe{sup 3+} ions, rather than Fe{sup 2+} ions, effectively eliminated RhB. Furthermore, the UV–vis spectra showing new absorbance at ∼ 285 nm indicate the complexes of RhB and Fe{sup 3+} ions, adopting vis photons to form excited state and further eject one electron via ligand-to-metal charge-transfer to activate H{sub 2}O{sub 2}. Additionally, efficient TBBPA removal was obtained only in the presence of RhB. Accordingly, the s-Fe{sup 0}– based photo-Fenton-like process assisted with dyestuff wastewater is promising for removing a series of persistent organic pollutants.

Positive autoantibodies to ZnT8 indicate elevated risk for additional autoimmune conditions in patients with Addison's disease.

Science.gov (United States)

Fichna, Marta; Rogowicz-Frontczak, Anita; Żurawek, Magdalena; Fichna, Piotr; Gryczyńska, Maria; Zozulińska-Ziółkiewicz, Dorota; Ruchała, Marek

2016-07-01

Autoimmune Addison's disease (AAD) associates with exceptional susceptibility to develop other autoimmune conditions, including type 1 diabetes (T1D), marked by positive serum autoantibodies to insulin (IAA), glutamic acid decarboxylase (GADA) and insulinoma-associated protein 2 (IA-2A). Zinc transporter 8 (ZnT8) is a new T1D autoantigen, encoded by the SLC30A8 gene. Its polymorphic variant rs13266634C/T seems associated with the occurrence of serum ZnT8 antibodies (ZnT8A). This study was designed to determine the prevalence of serum ZnT8A and their clinical implication in 140 AAD patients. Other beta cell and thyroid-specific autoantibodies were also investigated, and ZnT8A results were confronted with the rs13266634 genotype. ZnT8A were detectable in 8.5 %, GADA in 20.7 %, IA-2A in 5.7 %, IAA in 1.6 % and various anti-thyroid antibodies in 7.1-67.8 % individuals. Type 1 diabetes was found in 10 % AAD patients. ZnT8A were positive in 57.1 % of T1D patients and 3.4 % non-diabetic AAD. Analysis of ZnT8A enabled to identify autoimmunity in two (14.3 %) T1D individuals previously classified as autoantibody-negative. ZnT8A-positive patients revealed significantly higher number of autoimmune conditions (p < 0.001), increased prevalence of T1D (p < 0.001) and other beta cell-specific autoantibodies. Carriers of the rs13266634 T-allele displayed increased frequency (p = 0.006) and higher titres of ZnT8A (p = 0.002). Our study demonstrates high incidence of ZnT8A in AAD patients. ZnT8A are associated with coexisting T1D and predictive of T1D in non-diabetic subjects. Moreover, positive ZnT8A in AAD indicate elevated risk for additional autoimmune conditions. Autoantibodies to beta cell antigens, comprising ZnT8, could be included in routine screening panels in AAD.

The new barium zinc mercurides Ba3ZnHg10 and BaZn0.6Hg3.4 – Synthesis, crystal and electronic structure

International Nuclear Information System (INIS)

Schwarz, Michael; Wendorff, Marco; Röhr, Caroline

2012-01-01

The title compounds Ba 3 ZnHg 10 and BaZn 0.6 Hg 3.4 were synthesized from stoichiometric ratios of the elements in Ta crucibles. Their crystal structures, which both represent new structure types, have been determined using single crystal X-ray data. The structure of Ba 3 ZnHg 10 (orthorhombic, oP28, space group Pmmn, a=701.2(3), b=1706.9(8), c=627.3(3)pm, Z=2, R1=0.0657) contains folded 4 4 Hg nets, where the meshes form the bases of flat rectangular pyramids resembling the structure of BaAl 4 . The flat pyramids are connected via Hg–Zn/Hg bonds, leaving large channels at the folds, in which Ba(1) and Hg(2) atoms alternate. Whereas the remaining Hg/Zn atoms form a covalent 3D network of three- to five-bonded atoms with short M–M distances (273–301 pm; CN 9–11), the Hg(2) atoms in the channels adopt a comparatively large coordination number of 12 and increased distances (317–348 pm) to their Zn/Hg neighbours. In the structure of BaZn 0.6 Hg 3.4 (cubic, cI320, space group I4 ¯ 3d, a=2025.50(7) pm, Z=64, R1=0.0440), with a chemical composition not much different from that of Ba 3 ZnHg 10 , the Zn/Hg atoms of the mixed positions M(1/2) are arranged in an slightly distorted primitive cubic lattice with a 4×4×4 subcell relation to the unit cell. The 24 of the originating 64 cubes contain planar cis tetramers Hg(5,6) 4 with Hg in a nearly trigonal planar or tetrahedral coordination. In another 24 of the small cubes, two opposing faces are decorated by Hg(3,4) 2 dumbbells, two by Ba(2) atoms respectively. The third type of small cubes are centered by Ba(1) atoms only. The complex 3D polyanionic Hg/Zn network thus formed is compared with the Hg partial structure in Rb 3 Hg 20 applying a group-subgroup relation. Despite their different overall structures, the connectivity of the negatively charged Hg atoms, the rather metallic Zn bonding characteristic (as obtained from FP-LAPW band structure calculations) and the coordination number of 16 for all Ba cations

ZnFe2O4 Containing Nanoparticles: Synthesis and Magnetic Properties

Directory of Open Access Journals (Sweden)

Zālīte Ilmārs

2017-05-01

Full Text Available Solid solutions of Co1−xZnxFe2O4 and Ni1−xZnxFe2O4 (0 < x < 1 nanoparticles were synthesized by sol-gel self-propagating combustion method. The obtained single cubic phase product has a specific surface area 25 m2∙g−1 to 33 m2∙g−1 and crystallite size 25 nm to 40 nm. Lattice parameters change linearly from 8.371 A (CoFe2O4 and 8.337 A (NiFe2O4 to 8.431 A (ZnFe2O4. The saturation magnetization (Ms changes non-linearly from 60.8 emu∙g−1 (CoFe2O4, respectively, from 35.6 emu∙g−1 (NiFe2O4 to 3.3 emu∙g−1 (ZnFe2O4 reaching maximal value 76.1 emu∙g−1 for Co0.8Zn0.2Fe2O4 and 64.9 emu∙g−1 – for Ni0.6Zn0.4Fe2O4.

Thermal transformation of synthetic borax, Na2[B4O5(OH)4]x8H2O

International Nuclear Information System (INIS)

Abdullaev, G.K.

1981-01-01

Using the methods of high temperature roentgenography and derivatography thermal transformation of synthetic borax is studied. It is established that borax dehydration proceeds in four stages (50-80, 80-100, 100-150 and 150-500 deg C) with the formation of three intermediate crystalline hydrate forms (one stable and two unstable) and one final stable crystalline phase. The stable crystalline phases correspond to synthetic tincalconite Na 2 [B 4 O 5 (OH) 4 ]x3H 2 O and sodium tetraborate Na 2 B 4 O 7 . Thermal transformation of borax into tincalconite and sodium tetraborate is explained on the basis of their crystal structures [ru

Itinerant magnetism in CeRh3B2

DEFF Research Database (Denmark)

Eriksson, Olle; Johansson, Börje; Brooks, M. S. S.

1989-01-01

Spin-polarized energy-band calculations, including spin-orbit coupling in the band Hamiltonian, have been performed on CeRh3B2. Good agreement is obtained between theory and experiment concerning the magnetic moment. It is also found that the magnetic moment varies strongly with volume and from...

[Die baltischen Lande im Zeitalter der Reformation und Konfessionalisierung : Livland, Estland, Ösel, Ingermanland, Kurland und Lettgallen : Stadt, Land und Konfession 1500-1721. Teil 4. Hrsg. von Matthias Asche, Werner Buchholtz und Anton Schindlin

Index Scriptorium Estoniae

Maasing, Madis, 1984-

2013-01-01

Arvustus: Die baltischen Lande im Zeitalter der Reformation und Konfessionalisierung : Livland, Estland, Ösel, Ingermanland, Kurland und Lettgallen : Stadt, Land und Konfession 1500-1721. Teil 4. (Katholisches Leben und Kirchenreform im Zeitalter der Glaubensspaltung, 72). Hrsg. von Matthias Asche, Werner Buchholtz und Anton Schindling. Verlag Aschendorff. Münster 2012

Mutations in COQ8B (ADCK4) found in patients with steroid-resistant nephrotic syndrome alter COQ8B function

OpenAIRE

Fonseca, Luis Vazquez; Doimo, Mara; Calderan, Cristina; Desbats, Maria Andrea; Acosta, Manuel J.; Cerqua, Cristina; Cassina, Matteo; Ashraf, Shazia; Hildebrandt, Friedhelm; Sartori, Geppo; Navas, Placido; Trevisson, Eva; Salviati, Leonardo

2018-01-01

Abstract Mutations in COQ8B cause steroid‐resistant nephrotic syndrome with variable neurological involvement. In yeast, COQ8 encodes a protein required for coenzyme Q (CoQ) biosynthesis, whose precise role is not clear. Humans harbor two paralog genes: COQ8A and COQ8B (previously termed ADCK3 and ADCK4). We have found that COQ8B is a mitochondrial matrix protein peripherally associated with the inner membrane. COQ8B can complement a ΔCOQ8 yeast strain when its mitochondrial targeting sequenc...

Chemisorption of SO2 at the surface of In2O3 modified by zink

International Nuclear Information System (INIS)

Vinokurova, M.V.; Derlyukova, L.E.; Vinokurov, A.A.

2005-01-01

Chemisorption of SO 2 and O 2 at the surface of In 2 O 3 involving zink addition (0.4-2.7 at.%) are investigated in the temperature range 22-200 Deg C. No less than three forms of sorbed SO 2 are available at the surface of modified In 2 O 3 . Temperature effects on the ratio of forms of SO 2 sorption and, consequently, on varying the electric conductivity. Previous sorption of O 2 is favorable to the formation of donor form of chemisorbed SO 2 [ru

Interfacial microstructures and solder joint strengths of the Sn-8Zn-3Bi and Sn-9Zn-lAl Pb-free solder pastes on OSP finished printed circuit boards

Energy Technology Data Exchange (ETDEWEB)

Lin, C.-T. [Department of Materials Science and Engineering, National United University, 1 Lein-Da, Kung-Ching Li, Miaoli 36003, Taiwan (China); Electronics and Optoelectronics Research Laboratories, Industrial Technology Research Institute, 195 Section 4, Chung-Hsing Road, Chutung, Hsinchu 31040, Taiwan (China); Hsi, C.-S. [Department of Materials Science and Engineering, National United University, 1 Lein-Da, Kung-Ching Li, Miaoli 36003, Taiwan (China); Wang, M.-C. [Faculty of Fragrance and Cosmetics, Kaohsiung Medical University, 100 Shih-Chuan 1st Road, Kaohsiung 807, Taiwan (China)], E-mail: mcwang@kmu.edu.tw; Chang, T.-C.; Liang, M.-K. [Electronics and Optoelectronics Research Laboratories, Industrial Technology Research Institute, 195 Section 4, Chung-Hsing Road, Chutung, Hsinchu 31040, Taiwan (China)

2008-07-14

Two kinds of lead-free solders, Sn-8Zn-3Bi and Sn-9Zn-lAl, were used to mount passive components onto printed circuit boards via a re-flow soldering process. The samples were stored at 150 deg. C for 200, 400, 600, 800, and 1100 h. The microstructures of the samples after aged at 150 deg. C for various times were characterized using optical microscopy (OM), scanning electron microscopy (SEM), energy dispersive spectrometry (EDS) and the analyzed of solder joint shear strengths. The joint strength between Sn-8Zn-3Bi and Cu pad was about 4.0 {+-} 0.3 kg, while the strength between Sn-9Zn-lAl and Cu pad had values of 2.6 {+-} 0.1 kg. Both kinds of solder joints exhibited reduced strengths with increasing aging times. After aging at 150 deg. C for 1100 h, the joints strengths of Sn-8Zn-3Bi and Sn-9Zn-lAl were 1.8 {+-} 0.3 and 1.7 {+-} 0.3 kg, respectively. Both the Sn-8Zn-3Bi and Sn-9Zn-lAl joints showed brittle fracture behaviors. A flat layer of Cu{sub 5}Zn{sub 8} intermetallic compound (IMC) was formed between Sn-8Zn-3Bi solder and Cu pad after reflow. When the aging time was increased to 400 h, Zn-depletion and formation of Cu{sub 6}Sn{sub 5} IMC were observed in the solders due to the interaction between the tin and zinc compounds. The interaction between Sn-9Zn-lAl solder and Cu pad had similar behavior, however, Cu{sub 6}Sn{sub 5} IMC formed in Sn-9Zn-lAl solder when after aging at 150 deg. C for 600 h. As the aging time increased, both types of solders generated clear IMC spalling layers with large and continuous voids. Those voids substantially decreased the joint strength.

DEWEK '98: 4. German wind power conference; DEWEK '98: 4. Deutsche Windenergie-Konferenz. Tagungsband

Energy Technology Data Exchange (ETDEWEB)

Gerdes, B. [ed.

1999-07-01

The conference report comprises 90 papers and posters on the following subjects: 1. Technological developments (e.g. use of adaptive structures systems, active stalle wind power systems, systems for early detection of errors); 2. Design and optimisation; 3. Wind forecasts; 4. Operation analyses (e.g. active and passive stall, collective loads, wind power systems in cold climates); 5. Wind power systems and the environment; 6. Offshore wind power generation; 7. Electric characteristics (e.g. modelling of flicker, energy conditioning in distribution systems with a high wind power share); 8. Economic efficiency (e.g. economic efficiency of offshore wind parks on the North Sea coast); 9. Network quality; 10. Rotor development (e.g. noise reduction); 11. Certification and methods of measurement. [German] Der Tagungsband enhaelt 90 Fach- und Posterbeitraege, die sich mit den folgenden Schwerpunkten befassen: 1. Technologische Entwicklungen (z.B. Einsatz von adaptiven Struktursystemen; Active-Stall-WKA; Fehlerfrueherkennungssystemen). 2. Auslegung und Optimierung. 3. Windprognosen. 4. Betriebsanalysen (z.B. Aktive Stall/Passive Stall im Vergleich; Lastkollektive von WKA; WKA in kaltem Klima). 5. Windenergieanlagen und Umwelt. 6. Offshore-Windenergienutzung. 7. Elektrische Eigenschaften (z.B. Modellierung des 'Flickerverhaltens' von WKA; Energiekonditionierung in Verteilnetzen mit hohem Windenergieanteil). 8. Wirtschaftlichkeit (z.B. Wirtschaftlichkeit von Offshore-Windparks der Norddeutschen Kuestenlinie). 9. Netzqualitaet. 10. Rotorentwicklung (z.B. Reduzierung der Schallabstrahlung von WKAs). 11. Zertifizierung von Messmethoden. (AKF)

Synthesis, band structure, and optical properties of Ba2ZnV2O8

International Nuclear Information System (INIS)

Chen, D.-G.; Cheng, W.-D.; Wu, D.-S.; Zhang, H.; Zhang, Y.-C.; Gong, Y.-J.; Kan, Z.-G.

2004-01-01

A novel compound Ba 2 ZnV 2 O 8 has been synthesized in high temperature solution reaction and its crystal structure has been characterized by means of single crystal X-ray diffraction analysis. It crystallizes in monoclinic system and belongs to space group P2 1 /c with a=7.9050(16), b=16.149(3), c=6.1580(12)A, β=90.49(3). It builds up from 1-D branchy chains of [ZnV 2 O 8 4- ] ∞ , and the Ba 2+ cations are located in the space among these chains. The IR spectrum, ultraviolet-visible diffuse reflection integral spectrum and fluorescent spectra of this compound have been investigated. The calculated results of energy band structure by the density functional theory method show that the solid-state compound of Ba 2 ZnV 2 O 8 is an insulator with direct band gap of 3.48eV. The calculated total and partial density of states indicate that the top valence bands are contributions from the mixings of O-2p, V-3d, and Zn-3d states and low conduction bands mostly originate from unoccupied antibonding states between the V-3d and O-2p states. The V-O bonds are mostly covalence characters and Zn-O bonds are mostly ionic interactions, and the ionic interaction strength is stronger between the Ba-O than between the Zn-O. The refractive index of n x , n y , and n z is estimated to be 1.7453, 1.7469, and 1.7126, respectively, at wavelength of 1060nm for Ba 2 ZnV 2 O 8 crystal

Intranasal LH-RH treatment of cryptorchidism. A clinical trial and 5 years follow-up

DEFF Research Database (Denmark)

Thorup, Jørgen Mogens; Mauritzen, K; Skakkebaek, N E

1987-01-01

The effect of intranasal LH-RH on cryptorchidism was investigated in 45 prepubertal boys with 68 undescended testes. A daily dose of 1.2 mg LH-RH was given for 4 weeks. A total of 16 testes (24%) descended. Follow-up examination 5 years later showed that relapse had occurred in two cases. Fifty......-two testes did not descend during the LH-RH treatment. However, seven of these testes descended spontaneously during puberty. So far surgical treatment has been carried out in 39 of the remaining 45 testes. Anatomical anomalies (ectopic position of the testis, open processus vaginalis, abnormal epididymis......) explained the failure of LH-RH to cause descent in the majority of the surgically treated cases....

Thermal Methane Conversion to Syngas Mediated by Rh1-Doped Aluminum Oxide Cluster Cations RhAl3O4.

Science.gov (United States)

Li, Ya-Ke; Yuan, Zhen; Zhao, Yan-Xia; Zhao, Chongyang; Liu, Qing-Yu; Chen, Hui; He, Sheng-Gui

2016-10-05

Laser ablation generated RhAl 3 O 4 + heteronuclear metal oxide cluster cations have been mass-selected using a quadrupole mass filter and reacted with CH 4 or CD 4 in a linear ion trap reactor under thermal collision conditions. The reactions have been characterized by state-of-the-art mass spectrometry and quantum chemistry calculations. The RhAl 3 O 4 + cluster can activate four C-H bonds of a methane molecule and convert methane to syngas, an important intermediate product in methane conversion to value-added chemicals. The Rh atom is the active site for activation of the C-H bonds of methane. The high electron-withdrawing capability of Rh atom is the driving force to promote the conversion of methane to syngas. The polarity of Rh oxidation state is changed from positive to negative after the reaction. This study has provided the first example of methane conversion to syngas by heteronuclear metal oxide clusters under thermal collision conditions. Furthermore, the molecular level origin has been revealed for the condensed-phase experimental observation that trace amounts of Rh can promote the participation of lattice oxygen of chemically very inert support (Al 2 O 3 ) to oxidize methane to carbon monoxide.

2,5-Bis[(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylsulfanyl]-1,3,4-thiadiazole

Directory of Open Access Journals (Sweden)

Gabriel Partl

2017-02-01

Full Text Available The title compound, C18H8F26N2S3, was obtained by double S-perfluorohexylethylation of dipotassium 1,3,4-thiadiazole-2,5-dithiolate in methanol. The molecule exhibits twofold rotational symmetry, with the S atom lying on the rotation axis. The fluorocarbon chains adopt helical conformations and the F atoms of the two terminal C atoms are disordered over two sets of sites. No directional intermolecular interactions occur in the crystal.

Dynamic MR imaging: Follow-up study after femoral head core decompression and rhBMP-2 instillation in patients with avascular necrosis of the femoral head; Dynamische Magnetresonanztomographie (MRT): Verlaufsbeobachtung nach Femurkerndekompression und Auffuellung mit rekombinantem, humanem Bone morphogenetic Protein-2 (rhBMP-2) bei avaskulaerer Femurkopfnekrose

Energy Technology Data Exchange (ETDEWEB)

Schedel, H. [Klinik Prof. Schedel, Kellberg (Germany); Schneller, A. [Humboldt-Universitaet, Berlin (Germany). Klinik fuer Allgemein- und Transplantationschirurgie; Vogl, T.; Mueller, H.F.; Maeurer, J.; Felix, R. [Humboldt-Universitaet, Berlin (Germany). Strahlenklinik und Poliklinik; Suedkamp, N. [Humboldt-Universitaet, Berlin (Germany). Unfall- und Wiederherstellungschirurgie; Eisenschenk, A. [Freie Univ. Berlin (Germany). Orthopaedische Klinik und Poliklinik

2000-07-01

Material and Methods: Six patients with avascular necrosis of the femoral head ARCO-stage I- or II-lesions were treated surgically by femoral head core decompression. Three of these patients were additionally treated with rhBMP-2-instillation. The progression or regression could be confirmed by T1- and T2-weighted spinecho-sequences (zero, four, ten, sixteen weeks and 24 months follow up). Results: Corresponding ARCO-classification with partly more sensitive measurement of vitality signs in comparison to the optical X-ray classification. The objective, quantitative measurement of signalintensity post contrast medium reduces the influence of experience and level of education. The dynamic sequences results are reproducable. (orig.) [German] Material und Methoden: Sechs Patienten mit avaskulaerer Nekrose des Femurkopfes des Stadiums I oder II nach ARCO wurden einer Femurkerndekompression unterzogen. Drei dieser Patienten erhielten zusaetzlich eine rhBMP-2-Auffuellung. Zum Zeitpunkt null, vier, zehn, sechszehn Wochen und 24 Monaten post OP erfolgte die kernspintomographische Untersuchung mit T1- und T2-gewichteten Sequenzen unter besonderer Beruecksichtigung der dynamischen Untersuchungssequenz nach Gabe von Gd-DTPA (Gadopentetsaeure, Dimegluminsalz; Magnevist {sup trademark}) zur Dokumentation der Signalintensitaetssteigerung pro Zeiteinheit in der Nekroseregion. Ergebnisse: Uebereinstimmende Stadienklassifikation nach ARCO mit zum Teil empfindlicherer Messung von Vitalitaetszeichen im Vergleich zu rein visuellen roentgenologischen Einteilung. Die objektive, quantitative Messung des Signalintensitaetssteigerungsverhaltens nach Kontrastmittelgabe im Bereich der Femurkopfnekrose kann den Einfluss von subjektiven Eigenschaften des Untersuchers (Erfahrung, Ausbildungsstand) reduzieren, wobei die Ergebnisse der Dynamiksequenzen objektiv reproduzierbar sind. (orig.)

Aminoacid N-substituted 1,4,7-triazacyclononane and 1,4,7,10-tetraazacyclododecane Zn2+, Cd2+ and Cu2+ complexes. A preparative, potentiometric titration and NMR spectroscopic study.

Science.gov (United States)

Plush, Sally E; Lincoln, Stephen F; Wainwright, Kevin P

2004-05-07

The pK(a)s and Zn2+, Cd2+ and Cu2+ complexation constants (K) for 1,4,7-tris[(2''S)-acetamido-2''-(methyl-3''-phenylpropionate)]-1,4,7-triazacyclononane, 1, 1,4,7-tris[(2''S)-acetamido-2''-(1''-carboxy-3''-phenylpropane)]-1,4,7-triazacyclononane, H(3)2, 1,4,7-tris[(2''S)-acetamido-2''-(methyl-3''-(1H-3-indolyl)propionate)]-1,4,7-triazacyclononane, 3, and 1,4,7,10-tetrakis[(2''S)-acetamido-2''-(methyl-3''-phenylpropionate)]-1,4,7,10-tetraazacyclododecane, 4, 1,4,7,10-tetrakis[(2''S)-acetamido-2''-(1''-carboxy-3''-phenylpropane)]-1,4,7,10-tetraazacyclododecane, H(4)5, in 20 : 80 v/v water-methanol solution are reported. The pK(a)s within the potentiometric detection range for H(3)1(3+) = 8.69 and 3.59, for H(6)2(3+) = 9.06, 6.13, 4.93 and 4.52, H(3)3(3+) = 8.79 and 3.67, H(4)4(4+) = 8.50, 5.62 and 3.77 and for H(8)5(4+) = 9.89, 7.06, 5.53, 5.46, 4.44 and 4.26 where each tertiary amine nitrogen is protonated. The complexes of 1: [Zn(1)]2+(9.00), [Cd(1)]2+ (6.49), [Cd(H1)]3+ (4.54) and [Cu(1)]2+ (10.01) are characterized by the log(K/dm3 mol(-1)) values shown in parentheses. Analogous complexes are formed by 3 and 4: [Zn(3)]2+ (10.19), [Cd(3)]2+ (8.54), [Cu(3)]2+ (10.77), [Zn(4)]2+ (11.41) [Cd(4)]2+ (9.16), [Cd(H4)]3+ (6.16) and [Cu(4)]2+ (11.71). The tricarboxylic acid H(3)2 generates a greater variety of complexes as exemplified by: [Zn(2)-] (10.68) [Zn(H2)] (6.60) [Zn(H(2)2)+] (5.15), [Cd(2)](-) (4.99), [Cd(H2)] (4.64), [Cd(H2(2))]+ (3.99), [Cd(H(3)2)]2+ (3.55), [Cu(2)](-) (12.55) [Cu(H2)] (7.66), [Cu(H(2)2)]+ (5.54) and [Cu(2)2](4-) (3.23). The complexes of H(4)5 were insufficiently soluble to study in this way. The 1H and 13C NMR spectra of the ligands are consistent with formation of a predominant Zn2+ and Cd2+ Delta or Lambda diastereomer. The preparations of the new pendant arm macrocycles H(3)2, 3, 4 and H(4)5 are reported.

The germanides Er{sub 5}Pd{sub 4}Ge{sub 8} and Tm{sub 5}Pd{sub 4}Ge{sub 8}. 3D [Pd{sub 4}Ge{sub 8}] polyanions with Ge{sub 2} dumb-bells and Ge{sub 4} chains in cis-conformation

Energy Technology Data Exchange (ETDEWEB)

Heying, Birgit; Rodewald, Ute C.; Poettgen, Rainer [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie

2017-07-01

Tm{sub 5}Pd{sub 4}Ge{sub 8} was synthesized by melting of the elements in an arc-melting furnace. The new germanide was characterized by powder and single-crystal X-ray diffraction: own structure type, P2{sub 1}/m, a=574.3(1), b=1380.4(3), c=836.4(1) pm, β=107.57(2) , V=0.6321 nm{sup 3}, wR2=0.0578, 2533 F{sup 2} values, 86 variables. The palladium and germanium atoms built up a three-dimensional [Pd{sub 4}Ge{sub 8}]{sup 15-} polyanionic network which contains a unique germanium substructure composed of the Zintl anions Ge{sub 2}{sup 6-} dumb-bells and Ge{sub 4}{sup 10-} chains in cis-conformation. The palladium atoms within the network have distorted square pyramidal germanium coordination. The three crystallographically independent thulium atoms have coordination numbers 15, 16 and 17 with partial motifs of the Frank-Kasper type polyhedra. The isotypic germanide Er{sub 5}Pd{sub 4}Ge{sub 8} forms only after annealing the arc-melted sample at 1070 K for 1 week: a=575.14(9), b=1386.3(3), c=838.4(1) pm, β=107.51(2) , V=0.6375 nm{sup 3}.

Thin film assembly of nano-sized Zn(II)-8-hydroxy-5,7-dinitroquinolate by using successive ion layer adsorption and reaction (SILAR) technique: characterization and optical-electrical-photovoltaic properties.

Science.gov (United States)

Farag, A A M; Haggag, Sawsan M S; Mahmoud, Mohamed E

2012-07-01

A method is described for thin film assembly of nano-sized Zn(II)-8-hydroxy-5,7-dinitroquinolate complex, Zn[((NO(2))(2)-8HQ)(2)] by using successive ion layer adsorption and reaction (SILAR) technique. Highly homogeneous assembled nano-sized metal complex thin films with particle size distribution in the range 27-47nm was identified by using scanning electron microscopy (SEM). Zn[((NO(2))(2)-8HQ)(2)] and [(NO(2))(2)-8HQ] ligand were studied by thermal gravimetric analysis (TGA). Graphical representation of temperature dependence of the dark electrical conductivity produced two distinct linear parts for two activation energies at 0.377eV and 1.11eV. The analysis of the spectral behavior of the absorption coefficient in the intrinsic absorption region reveals a direct allowed transition with a fundamental band gap of 2.74eV. The dark current density-voltage (J-V) characteristics showed the rectification effect due to the formation of junction barrier of Zn[((NO(2))(2)-8HQ)(2)] complex film/n-Si interface. The photocurrent in the reverse direction is strongly increased by photo-illumination and the photovoltaic characteristics were also determined and evaluated. Copyright © 2012 Elsevier B.V. All rights reserved.

RhNAC2 and RhEXPA4 Are Involved in the Regulation of Dehydration Tolerance during the Expansion of Rose Petals1[C][W][OA

Science.gov (United States)

Dai, Fanwei; Zhang, Changqing; Jiang, Xinqiang; Kang, Mei; Yin, Xia; Lü, Peitao; Zhang, Xiao; Zheng, Yi; Gao, Junping

2012-01-01

Dehydration inhibits petal expansion resulting in abnormal flower opening and results in quality loss during the marketing of cut flowers. We constructed a suppression subtractive hybridization library from rose (Rosa hybrida) flowers containing 3,513 unique expressed sequence tags and analyzed their expression profiles during cycles of dehydration. We found that 54 genes were up-regulated by the first dehydration, restored or even down-regulated by rehydration, and once again up-regulated by the second dehydration. Among them, we identified a putative NAC family transcription factor (RhNAC2). With transactivation activity of its carboxyl-terminal domain in yeast (Saccharomyces cerevisiae) cell and Arabidopsis (Arabidopsis thaliana) protoplast, RhNAC2 belongs to the NAC transcription factor clade related to plant development in Arabidopsis. A putative expansin gene named RhEXPA4 was also dramatically up-regulated by dehydration. Silencing RhNAC2 or RhEXPA4 in rose petals by virus-induced gene silencing significantly decreased the recovery of intact petals and petal discs during rehydration. Overexpression of RhNAC2 or RhEXPA4 in Arabidopsis conferred strong drought tolerance in the transgenic plants. RhEXPA4 expression was repressed in RhNAC2-silenced rose petals, and the amino-terminal binding domain of RhNAC2 bound to the RhEXPA4 promoter. Twenty cell wall-related genes, including seven expansin family members, were up-regulated in Arabidopsis plants overexpressing RhNAC2. These data indicate that RhNAC2 and RhEXPA4 are involved in the regulation of dehydration tolerance during the expansion of rose petals and that RhEXPA4 expression may be regulated by RhNAC2. PMID:23093360

Synthesis of Zn(BH{sub 4}){sub 2} and Gas Absorption and Release Characteristics of Zn(BH{sub 4}){sub 2}, Ni, or Ti-Added MgH{sub 2}–Based Alloys

Energy Technology Data Exchange (ETDEWEB)

Kwak, Young Jun; Lee, Seong Ho; Kwon, Sung Nam; Park Il Woo; Song, Myoung Youp [Chonbuk National University, Jeonju (Korea, Republic of)

2015-07-15

A sample [named Zn(BH{sub 4}){sub 2}(+NaCl)] was synthesized by milling ZnCl{sub 2} and NaBH{sub 4} at 400 rpm under argon gas for 2 h. And Zn(BH{sub 4}){sub 2}(+NaCl)+MgH{sub 2} sample was prepared by milling MgH{sub 2} in a planetary ball mill and mixing with the Zn(BH{sub 4}){sub 2}(+NaCl) synthesized by milling for 4 h in a mortar with a pestle. Then the gas-release characteristics of the two samples were investrigated. Analyses of XRD patterns and FT-IR spectra, as well as TGA, DTA, and SEM observations, were also performed. After heating the samples to 400 ℃, the weight losses of Zn(BH{sub 4}){sub 2}(+NaCl) and Zn(BH{sub 4}){sub 2}(+NaCl)+MgH{sub 2} were 11.2 and 8.2 wt%, respectively, with respect to the sample weight. The DTA results for the two samples showed a decomposition peak for Zn(BH{sub 4}){sub 2} at about 61 ℃. The DTA result of Zn(BH{sub 4}){sub 2}(+NaCl) + MgH{sub 2} showed a decomposition peak for MgH{sub 2} at about 374 ℃. A sample of Zn(BH{sub 4}){sub 2}(+NaCl)+MgH{sub 2} to which Ni, and Ti were added, with a composition of 90 wt% MgH{sub 2}-5 wt% Zn(BH{sub 4}){sub 2}(+NaCl)-2.5 wt% Ni-2.5 wt% Ti, in which a large amount of MgH2 is contained in order to make a large quantity of hydrogen be absorbed and released reversibly, was also prepared. The experimental results showed that addition of Zn(BH{sub 4}){sub 2}(+NaCl), Ni, or Ti increased the dehydriding rate of MgH{sub 2}, while decreased its initial hydriding rate.

Investigation on Al(III) and Zn(II) complexes containing a calix[4]arene bearing two 8-oxyquinoline pendant arms used as emitting materials for OLEDs

International Nuclear Information System (INIS)

Bagatin, Izilda A.; Legnani, Cristiano; Cremona, Marco

2009-01-01

A comparison between [Al·1] 3+ and [Zn·1] 2+ complexes (1 = 5,11,17,23-tetra-tert-butyl-25,27-bis[(quinoline-8-oxy)propyloxy]-26, 28-dihydroxy-calix[4]arene) has been made using electrochemical techniques and the experimental results obtained in the fabrication of organic light emitting devices (OLEDs). The electrochemically determined values of the ionization potential I p and electron affinity E a parameters for the [Al·1] 3+ (I p = 5.82eV, E a = 2.80eV) and [Zn·1] 2+ (I p = 5.67eV, E a = 2.32eV) evidenced that the [Al·1] 3+ complex is a better electron transporting layer with respect to the Zn complex one. The fabricated OLEDs based on these supramolecular complexes show a superior quality with the [Al·1] 3+ systems expected from the energy level diagrams

Formalin-inactivated EV71 vaccine candidate induced cross-neutralizing antibody against subgenotypes B1, B4, B5 and C4A in adult volunteers.

Directory of Open Access Journals (Sweden)

Ai-Hsiang Chou

Full Text Available Enterovirus 71 (EV71 has caused several epidemics of hand, foot and mouth diseases (HFMD in Asia. No effective EV71 vaccine is available. A randomized and open-label phase I clinical study registered with ClinicalTrials.gov #NCT01268787, aims to evaluate the safety, reactogenicity and immunogenicity of a formalin-inactivated EV71 vaccine candidate (EV71vac at 5- and 10-µg doses. In this study we report the cross-neutralizing antibody responses from each volunteer against different subgenotypes of EV71 and CVA16.Sixty eligible healthy adults were recruited and vaccinated. Blood samples were obtained on day 0, 21 and 42 and tested against B1, B4, B5, C2, C4A, C4B and CVA16 for cross-neutralizing antibody responses.The immunogenicity of both 5- and 10- µg doses were found to be very similar. Approximately 45% of the participants had 4-fold increase in Nt, but there was no further increase in Nt after the second dose. EV71vac induced very strong cross-neutralizing antibody responses in >85% of volunteers without pre-existing Nt against subgenotype B1, B5 and C4A. EV71vac elicited weak cross-neutralizing antibody responses (∼20% of participants against a C4B and Coxsackie virus A16. Over 90% of vaccinated volunteers did not develop cross-neutralizing antibody responses (Nt<8 against a C2 strain. EV71vac can boost and significantly enhance the neutralizing antibody responses in volunteers who already had pre-vaccination antibodies against EV71 and/or CVA16.EV71vac is efficient in eliciting cross-neutralizing antibody responses against EV71 subgenotypes B1, B4, B5, and C4A, and provides the rationale for its evaluation in phase II clinical trials.ClinicalTrials.gov NCT01268787.

Harmful loading of water courses caused by precipitation. Phase 2. Part project 8: Loading of harmful substances by precipitation. Pt. A, B, and C. Pt. A: Harmful substances introduced by atmospheric deposition dust.Pt. B: Sources and mobility of harmful substances. Pt. C: Load of harmful substances from roof and road surfaces; NIEDERschlagsbedingte SCHadstoffbeLAstung der Gewaesser - Phase 2. Teilprojekt 8: Schadstoffbelastung durch Niederschlag. T. A, B und C. T. A: Schadstoffeintrag durch atmosphaerische Staubdeposition. T. B: Quellen und Mobilitaet von Schadstoffen. T. C: Schadstofffrachten von Dach- und Strassenflaechen. Abschlussbericht

Energy Technology Data Exchange (ETDEWEB)

Luetzner, K.; Grothkopp, H.; Gebhard, V.; Rennert, S.; Huth, B.

1997-02-28

Stadtgebieten ist die Belastung der Oberflaechenabfluesse nicht allein von der Verkehrsdichte abhaengig. Dies gilt hoechstens ueber die Partikelbeladung hinsichtlich einiger Elemente. Das Fahrverhalten, z.B. haeufiges Anfahren und Bremsen, ist hier ebenso von Bedeutung. Weiterhin beeinflussen die Hintergrundbelastung, Abspuelungen von unbefestigten Flaechen sowie weitere Aktivitaeten (z.B. intensive Bautaetigkeit) die Belastung von Nebenstrassen. Im Verlauf der untersuchten Niederschlagsereignisse war nach ca. 6 mm Niederschlag die Auswaschung der bodennahen Luftschicht beendet. Nach einem gefallenen Niederschlag von jeweils 15 mm konnte bei zwei Ereignissen die nahezu vollstaendige Abspuelung der partikulaeren Fracht festgestellt werden. Rund 80% der Schwermetallbelastung (bei Cu nur ca. 50%) des Einzugsgebietes werden durch die Emissionen des Strassenverkehrs verursacht. Kupferdaecher emittieren rund 40% der Cu-Fracht. Die Schwermetallfracht der Dachabfluessen ist ueberwiegend in der fluessigen Phase enthalten (ausser Pb, Fe), dagegen ist die Fracht der Strassenabfluesse zu ueber 90% partikulaer gebunden. Ein Rueckhalt dieser Schwermetallfracht koennte somit ueber den AFS-Rueckhalt geschehen. Entsprechend der durchgefuehrten Berechnung auf Grundlage bekannter Mittelwerte entfernt die Stadtreinigung Dresden gegenwaertig etwa die Haelfte der Fe- und Ni-Gesamtfracht sowie rund 40% der Cu-, Pb- und Zn-Gesamtfracht des Einzugsgebietes. (orig./AJ)

Structure of a zinc oxide ultra-thin film on Rh(100)

Energy Technology Data Exchange (ETDEWEB)

Yuhara, J.; Kato, D.; Matsui, T. [Department of Materials, Physics and Energy Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603 (Japan); Mizuno, S. [Department of Molecular and Material Sciences, Kyushu University, Kasuga, Fukuoka 816–8580 (Japan)

2015-11-07

The structural parameters of ultra-thin zinc oxide films on Rh(100) are investigated using low-energy electron diffraction intensity (LEED I–V) curves, scanning tunneling microscopy (STM), and first-principles density functional theory (DFT) calculations. From the analysis of LEED I–V curves and DFT calculations, two optimized models A and B are determined. Their structures are basically similar to the planer h-BN ZnO(0001) structure, although some oxygen atoms protrude from the surface, associated with an in-plane shift of Zn atoms. From a comparison of experimental STM images and simulated STM images, majority and minority structures observed in the STM images represent the two optimized models A and B, respectively.

Development and verification of a pharmacokinetic model to optimize physiologic replacement of rhIGF-1/rhIGFBP-3 in preterm infants.

Science.gov (United States)

Chung, Jou-Ku; Hallberg, Boubou; Hansen-Pupp, Ingrid; Graham, Martin A; Fetterly, Gerald; Sharma, Jyoti; Tocoian, Adina; Kreher, Nerissa C; Barton, Norman; Hellström, Ann; Ley, David

2017-03-01

rhIGF-1/rhIGFBP-3 is being investigated for prevention of retinopathy of prematurity in extremely preterm infants. A population pharmacokinetic model was developed using data from phase I/II (Sections A-C) trials of rhIGF-1/rhIGFBP-3 and additional studies in preterm infants to predict optimal dosing to establish/maintain serum IGF-1 within physiological intrauterine levels. In Section D of the phase II study, infants (gestational age (GA) (wk+d) 23+0 to 27+6) were randomized to rhIGF-1/rhIGFBP-3, administered at the model-predicted dose of 250 µg/kg/d continuous i.v. infusion up to postmenstrual age (PMA) 29 wk+6 d or standard of care. An interim pharmacokinetic analysis was performed for the first 10 treated infants to verify dosing. Serum IGF-1 data were reviewed for 10 treated/9 control infants. Duration of therapy in treated infants ranged 1-34.5 d. At baseline (before infusion and <24 h from birth), mean (SD) IGF-1 was 19.2 (8.0) μg/l (treated) and 15.4 (4.7) μg/l (controls). Mean (SD) IGF-1 increased to 45.9 (19.6) μg/l at 12 h in treated infants, and remained within target levels for all subsequent timepoints. For treated infants, 88.8% of the IGF-1 measurements were within target levels (controls, 11.1%). Through the reported work, we determined appropriate rhIGF-1/rhIGFBP-3 dosing to achieve physiological intrauterine serum IGF-1 levels in extremely preterm infants.

UV and humidity sensing properties of ZnO nanorods prepared by the arc discharge method

International Nuclear Information System (INIS)

Fang, F; Futter, J; Markwitz, A; Kennedy, J

2009-01-01

The UV and humidity sensing properties of ZnO nanorods prepared by arc discharge have been studied. Scanning electron microscopy and photoluminescence spectroscopy were carried out to analyze the morphology and optical properties of the as-synthesized ZnO nanorods. Proton induced x-ray emission was used to probe the impurities in the ZnO nanorods. A large quantity of high purity ZnO nanorod structures were obtained with lengths of 0.5-1 μm. The diameters of the as-synthesized ZnO nanorods were found to be between 40 and 400 nm. The nanorods interlace with each other, forming 3D networks which make them suitable for sensing application. The addition of a polymeric film-forming agent (BASF LUVISKOL VA 64) improved the conductivity, as it facilitates the construction of conducting networks. Ultrasonication helped to separate the ZnO nanorods and disperse them evenly through the polymeric agent. Improved photoconductivity was measured for a ZnO nanorod sensor annealed in air at 200 deg. C for 30 min. The ZnO nanorod sensors showed a UV-sensitive photoconduction, where the photocurrent increased by nearly four orders of magnitude from 2.7 x 10 -10 to 1.0 x 10 -6 A at 18 V under 340 nm UV illumination. High humidity sensitivity and good stability were also measured. The resistance of the ZnO nanorod sensor decreased almost linearly with increasing relative humidity (RH). The resistance of the ZnO nanorods changed by approximately five orders of magnitude from 4.35 x 10 11 Ω in dry air (7% RH) to about 4.95 x 10 6 Ω in 95% RH air. It is experimentally demonstrated that ZnO nanorods obtained by the arc discharge method show excellent performance and promise for applications in both UV and humidity sensors.

Highly recyclable and ultra-rapid catalytic reduction of organic pollutants on Ag-Cu@ZnO bimetal nanocomposite synthesized via green technology

Science.gov (United States)

Gangarapu, Manjari; Sarangapany, Saran; Suja, Devipriya P.; Arava, Vijaya Bhaskara Rao

2018-04-01

In this study, synthesis of Ag-Cu alloy bimetal nanoparticles anchored on high surface and porous ZnO using a facile, greener and low-cost aqeous bark extract of Aglaia roxburghiana for highly active, ultra-rapid and stable catalyst is performed. The nanocomposite was scrupulously characterized using UV-Vis spectrophotometer, X-ray diffraction, Raman spectrophotometer, high-resolution transmission electron microscope, selected area (electron) diffraction, scanning electron microscope with energy dispersive X-ray spectroscopy, and Fourier-transform infrared spectroscopy. The catalytic activity of the green synthesized Ag-Cu bimetal nanocomposite was evaluated in the reduction of 4-nitrophenol (4-NP), methylene blue (MB) and rhodamine B (Rh B) dyes. The different types of dye exhibited very high and effective catalytic activity within few seconds. The theoretical investigations reveal that the unique synergistic effect of Ag-Cu nanoparticles and immobilization over ZnO assists in the reduction of 4-NP, MB and Rh B. Loading and leaching of metal nanoparticles were obtained using inductively coupled plasma atomic emission spectroscopy. Moreover, the stable and efficient recyclability of nanocomposite by centrifugation after completion of the reaction was demonstrated. The results lead to the design different possible bimetal on ZnO with boosting and an effective catalyst for the environmental applications.

Synthesis of Zn{sup 2+} doped BiOCl hierarchical nanostructures and their exceptional visible light photocatalytic properties

Energy Technology Data Exchange (ETDEWEB)

Li, Wen Ting [Department of Chemistry, Fujian Normal University, Fuzhou 350007 (China); Huang, Wan Zhen; Zhou, Huan [Research Center of Analysis and Measurement, Zhejiang University of Technology, Hangzhou 310014 (China); Yin, Hao Yong [Institute of Environmental Science and Engineering, Hangzhou Dianzi University, Hangzhou 310018 (China); Zheng, Yi Fan [Research Center of Analysis and Measurement, Zhejiang University of Technology, Hangzhou 310014 (China); Song, Xu Chun, E-mail: songxuchunfj@163.com [Department of Chemistry, Fujian Normal University, Fuzhou 350007 (China)

2015-07-25

Highlights: • Hierarchical-structured Zn-doped BiOCl were prepared by a facile solvothermal method. • The Zn-doped BiOCl showed higher photocatalytic ability than other BiOCl materials. • The effects of Zn-doping contents on the photocatalytic activity were discussed. • Repetitive tests implied the good stability of the Zn-doped BiOCl photocatalyst. - Abstract: In this study, BiOCl doped with different contents of zinc were successfully prepared via a facile ethylene glycol (EG)-assisted solvothermal process at 160 °C for 12 h. The as-synthesized samples were characterized in details by X-ray powder diffraction (XRD), energy dispersive X-ray analysis (EDS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), UV–vis diffuse reflectance spectra (UV–vis DRS) and Brunauer Emmet Teller (BET) measurement. The photocatalytic performances were evaluated by the photocatalytic degradation of Rhodamine B (RhB) under visible light irradiation. The results showed that Zn doping did not change the morphologies and particle sizes of BiOCl. However, it had an obvious effect on the photocurrent and BET surface area of BiOCl and accordingly the photocatalytic performance of BiOCl was greatly improved. The Zn-doped BiOCl with R{sub Zn} = 0.07 showed the highest photocatalytic activities with almost all of the RhB decomposed in 8 min. Moreover, repetitive tests imply the good recyclability and stability of the catalysts. The enhanced photocatalytic activity was largely ascribed to the efficient separation of photogenerated electron–hole pairs and high BET surface area of the catalysts. In addition, a possible mechanism on basis of the experimental results was discussed.

Adsorption of methane on Zn(bdc)(ted)0.5 microporous metal-organic framework

Science.gov (United States)

Krungleviciute, Vaiva; Pramanik, Sanhita; Migone, Aldo; Li, Jing

2011-03-01

Zn(bdc)(ted)0.5 is metal-organic framework crystallized in a tetragonal space group with a 3D porous structure containing intersecting channels of two different sizes. The larger channels are parallel to the c axis and have a cross section 7.5 × 7.5 AA. The smaller channels are along both the a- and b-axes and have a cross section of 4.8 × 3.2 AA. We measured methane adsorption isotherms at several different temperatures between 82 and 102 K. We calculated the effective specific surface area, isosteric heat and binding energy values. Two distinct substeps were observed in the isotherms corresponding to two different adsorption sites. The origin of the substeps will be discussed.

Effect of ZnO Nanoparticles on the Sintering Behavior and Physical Properties of Bi0.5(Na0.8K0.2)0.5TiO3 Lead-Free Ceramics

Science.gov (United States)

Vuong, Le Dai; Truong-Tho, Nguyen

2017-11-01

Sintered Bi0.5(Na0.8K0.2)0.5TiO3 + x wt.% ZnO nanoparticle (BNKT- xZnOn) ceramics have been fabricated by conventional annealing with the aid of ultrasound waves for preliminary milling. Because of the presence of the liquid Bi2O3-ZnO phase at the eutectic point of 738°C, the sintering temperature decreased from 1150°C to 1000°C, and the morphology phase boundary of BNKT- xZnOn ceramics can be clarified by two separated peaks at (002)T and (200)T of 2 θ in the x-ray diffraction (XRD) patterns. The improvement of ferroelectric properties has been obtained for BNZT-0.2 wt.% ZnOn ceramics by the increase of remanent polarization up to 20.4 μC/cm2 and a decrease of electric coercive field down to 14.2 kV/cm. The piezoelectric parameters of the ceramic included a piezoelectric charge constant of d 31 = 78 pC/N; electromechanical coupling factors k p = 0.31 and k t = 0.34, larger than the values of 42 pC/N, 0.12 and 0.13, respectively, were obtained for the BNKT ceramics.

Characterization of detectors of neutrons from B+ZnS (Ag) as an alternative to 3He detectors

International Nuclear Information System (INIS)

Gonzalez, Juan A.; Suarez, Maria J.; Pujol, Luis; Lorente, Alfredo; Gallego, Eduardo

2013-01-01

The objective of this paper is to present the progress made in the design of prototypes for dynamic detection of neutron detectors based on scintillation of B + ZnS (Ag), which can replace existing 3 He detectors for the detection of illicit traffic of radioactive material and special nuclear material. These detectors B + ZnS (Ag) can be used, together with gamma detectors, PVT and NaI (Tl) also developed in the UPM. Two neutron detectors of different shapes and sizes were characterized using two neutron sources of 241 Am + Be. Were determined depth, overall efficiency, intrinsic efficiency and limit of detection. The results of these tests allow to verify that: 1) two cylindrical detectors B + ZnS (Ag) of 5x68 cm, or 4x15x132 cm rectangular detector can replace the cylindrical detector of 5x180 cm 3 He currently employed in the arcades. 2) the dynamic detection limit obtained is less than 20000 neutrons per second, when the sample becomes 2 m to 2m/s, with a probability of having no false positive or negative of the 99.99% 3) digital electronics eliminates interference from gamma emissions samples when their dose rate in the neutron detector is 65 μSv/h in less than factor 10 - 8, and keeps its detection limit and 4) two cylindrical detectors with two moderators of different thickness, of 25 to 50 mm of high density polyethylene, allow to measure the average energy of the neutrons

DSM-IV und DSM-5: Was hat sich tatsächlich verändert?

OpenAIRE

Ehret, Anna M.; Berking, Matthias

2013-01-01

Im Mai 2013 ist die fünfte Auflage des Diagnostischen und Statistischen Manuals Psychischer Störungen (DSM-5) der American Psychiatric Association erschienen. Um die Vor- und Nachteile des DSM-5 beurteilen und gegebenenfalls in Forschung und Praxis angemessen berücksichtigen zu können, sollten Wissenschaftler und Praktiker gleichermaßen über die Änderungen gegenüber dem DSM-IV informiert sein. In diesem Beitrag werden die wesentlichen Unterschiede zwischen dem DSM-IV und DSM-5 beschrieben. Ze...

Dual band monopole antenna for WLAN 2.4/5.2/5.8 with truncated ground

Science.gov (United States)

Chandan, Bharti, Gagandeep; Srivastava, Toolika; Rai, B. S.

2018-04-01

A dual-band mono-pole antenna is proposed for Wireless LAN applications. The WLAN band is obtained by cutting a rectangular ring and a circular slot in the radiating patch. The overall dimension of antenna is 17×16.5×0.8 mmł. The frequency bands obtained are 2.38-2.9 GHz and 4.7-6.1 GHz with ≤ - 10 dB return loss which covers WLAN 2.4/5.2/5.8 GHz bands. The behavior of the antenna is analyzed in terms of radiation pattern, peak realized gain, radiation efficiency and surface current density. It has dipole like radiation pattern with gain of 2.33 - 4.31 dBi for lower frequency band and 4.29 - 5.16 dBi for upper frequency band with radiation efficiency of 95-98% and 93-96% respectively. The parametric analysis is carried out to understand the consequence of the various shape parameters and to get an optimum design. The simulation and measurement gave the results having close agreement.

Ferrites Ni0,5Zn0,5Fe2O4 doped with samarium: structural analysis, morphological and electromagnetic

International Nuclear Information System (INIS)

Costa, A.C.F.M.; Diniz, A.P.; Viana, K.M.S.; Cornejo, D.R.; Kiminami, R.H.G.A.

2010-01-01

This paper proposes to investigate the sintering at 1200 deg C/2h of Ni 0.5 Zn 0.5 Fe 2-x Sm x O 4 ferrite doped with 0.05; 0.075 e 0.1 mol of Sm synthesized by combustion reaction to evaluate the performance materials as absorbers of electromagnetic radiation. The influence of the concentration of samarium on the structure, morphology and electromagnetic properties of ferrites was studied. The resulting samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), magnetic measurements and reflectivity measurements in the frequency range between 8-12 GHz. The results showed that increasing the concentration of samarium caused a decrease in particle size of the samples, encouraging, therefore, to obtain materials with better values of magnetization and reflectivity, allowing for use as absorbers in narrow-band frequency between 9-10 GHz. (author)

Radiation portal monitor with "1"0B+ZnS(Ag) neutron detector performance for the detection of special nuclear materials

International Nuclear Information System (INIS)

Guzman G, K. A.; Gallego, E.; Lorente, A.; Ibanez F, S.; Vega C, H. R.; Gonzalez, J. A.; Mendez, R.

2016-10-01

In homeland security, neutron detection is used to prevent the smuggling of special nuclear materials. Thermal neutrons are normally detected with "3He proportional counters, in the radiation portal monitors, Rpms, however due to the "3He shortage new procedures are being studied. In this work Monte Carlo methods, using the MCNP6 code, have been used to study the neutron detection features of a "1"0B+ZnS(Ag) under real conditions inside of a Rpm. The performance for neutron detection was carried out for "2"5"2Cf, "2"3"8U and "2"3"9Pu under different conditions. In order to mimic an actual situation occurring at border areas, a sample of SNM sited inside a vehicle was simulated and the Rpm with "1"0B+ZnS(Ag) response was calculated. At 200 cm the "1"0B+ZnS(Ag) on Rpm response is close to 2.5 cps-ng "2"5"2Cf, when the "2"5"2Cf neutron source is shielded with 0.5 cm-thick lead and 2.5 cm-thick polyethylene fulfilling the ANSI recommendations. Three different geometries of neutron detectors of "1"0B+ZnS(Ag) in a neutron detection system in Rpm were modeled. Therefore, the "1"0B+ZnS(Ag) detectors are an innovative and viable replacement for the "3He detectors in the Rpm. (Author)

Structure of malaria invasion protein RH5 with erythrocyte basigin and blocking antibodies.

Science.gov (United States)

Wright, Katherine E; Hjerrild, Kathryn A; Bartlett, Jonathan; Douglas, Alexander D; Jin, Jing; Brown, Rebecca E; Illingworth, Joseph J; Ashfield, Rebecca; Clemmensen, Stine B; de Jongh, Willem A; Draper, Simon J; Higgins, Matthew K

2014-11-20

Invasion of host erythrocytes is essential to the life cycle of Plasmodium parasites and development of the pathology of malaria. The stages of erythrocyte invasion, including initial contact, apical reorientation, junction formation, and active invagination, are directed by coordinated release of specialized apical organelles and their parasite protein contents. Among these proteins, and central to invasion by all species, are two parasite protein families, the reticulocyte-binding protein homologue (RH) and erythrocyte-binding like proteins, which mediate host-parasite interactions. RH5 from Plasmodium falciparum (PfRH5) is the only member of either family demonstrated to be necessary for erythrocyte invasion in all tested strains, through its interaction with the erythrocyte surface protein basigin (also known as CD147 and EMMPRIN). Antibodies targeting PfRH5 or basigin efficiently block parasite invasion in vitro, making PfRH5 an excellent vaccine candidate. Here we present crystal structures of PfRH5 in complex with basigin and two distinct inhibitory antibodies. PfRH5 adopts a novel fold in which two three-helical bundles come together in a kite-like architecture, presenting binding sites for basigin and inhibitory antibodies at one tip. This provides the first structural insight into erythrocyte binding by the Plasmodium RH protein family and identifies novel inhibitory epitopes to guide design of a new generation of vaccines against the blood-stage parasite.

The N2O activation by Rh5 clusters. A quantum chemistry study.

Science.gov (United States)

Olvera-Neria, Oscar; Avilés, Roberto; Francisco-Rodríguez, Héctor; Bertin, Virineya; García-Cruz, Raúl; González-Torres, Julio César; Poulain, Enrique

2015-04-01

Nitrous oxide (N2O) is a by-product of exhaust pipe gases treatment produced by motor vehicles. Therefore, the N2O reduction to N2 is necessary to meet the actual environmental legislation. The N2O adsorption and dissociation assisted by the square-based pyramidal Rh5 cluster was investigated using the density functional theory and the zero-order regular approximation (ZORA). The Rh5 sextet ground state is the most active in N2O dissociation, though the quartet and octet states are also active because they are degenerate. The Rh5 cluster spontaneously activates the N2─O cleavage, and the reaction is highly exothermic ca. -75 kcal mol(-1). The N2─O breaking is obtained for the geometrical arrangement that maximizes the overlap and electron transfers between the N2O and Rh5 frontier orbitals. The Rh5 high activity is due to the Rh 3d orbitals are located between the N2O HOMO and LUMO orbitals, which makes possible the interactions between them. In particular, the O 2p states strongly interact with Rh 3d orbitals, which finally weaken the N2─O bond. The electron transfer is from the Rh5 HOMO orbital to the N2O antibonding orbital.

Rhenium (5) and molybdenum (5) complexes with 4',4''(5'')-ditretbutyldibenzo-24-crown-8

International Nuclear Information System (INIS)

Ashurova, N.Kh.; Yakubov, K.G.; Basitova, S.M.; Tashmukhamedova, A.K.; Sajfullina, N.Zh.

1989-01-01

Rhenium and molybdenum complexes in +5 oxidation degree with 4',4''(5'')-ditretbutyldibenzo-24-crown-8 (L) are synthesized with 75-95 % yield. Composition and structure of compounds produced are investigated using element analysis, conductometry, IR spectroscopy, thermogravimetry methods. Oxidation degree of complexer metal is determined. It is ascertained that the compound composition corresponds to the MOLX 3 formula, where M-Re, Mo; X-Cl - , Br -

High-pressure synthesis and characterization of new actinide borates, AnB4O8 (An=Th, U).

Science.gov (United States)

Hinteregger, Ernst; Hofer, Thomas S; Heymann, Gunter; Perfler, Lukas; Kraus, Florian; Huppertz, Hubert

2013-11-18

New actinide borates ThB4O8 and UB4O8 were synthesized under high-pressure, high-temperature conditions (5.5 GPa/1100 °C for thorium borate, 10.5 GPa/1100 °C for the isotypic uranium borate) in a Walker-type multianvil apparatus from their corresponding actinide oxide and boron oxide. The crystal structure was determined on basis of single-crystal X-ray diffraction data that were collected at room temperature. Both compounds crystallized in the monoclinic space group C2/c (Z=4). Lattice parameters for ThB4O8: a=1611.3(3), b=419.86(8), c=730.6(2) pm; β=114.70(3)°; V=449.0(2) Å(3); R1=0.0255, wR2=0.0653 (all data). Lattice parameters for UB4O8: a=1589.7(3), b=422.14(8), c=723.4(2) pm; β=114.13(3)°; V=443.1(2) Å(3); R1=0.0227, wR2=0.0372 (all data). The new AnB4O8 (An=Th, U) structure type is constructed from corner-sharing BO4 tetrahedra, which form layers in the bc plane. One of the four independent oxygen atoms is threefold-coordinated. The actinide cations are located between the boron-oxygen layers. In addition to Raman spectroscopic investigations, DFT calculations were performed to support the assignment of the vibrational bands. © 2013 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This isan open access article under the terms of the Creative Commons AttributionLicense, which permits use, distribution and reproduction in any medium,provided the original work is properly cited.

RH-TRU Waste Content Codes

Energy Technology Data Exchange (ETDEWEB)

Washington TRU Solutions

2007-07-01

The Remote-Handled Transuranic (RH-TRU) Content Codes (RH-TRUCON) document describes the inventory of RH-TRU waste within the transportation parameters specified by the Remote-Handled Transuranic Waste Authorized Methods for Payload Control (RH-TRAMPAC).1 The RH-TRAMPAC defines the allowable payload for the RH-TRU 72-B. This document is a catalog of RH-TRU 72-B authorized contents by site. A content code is defined by the following components: • A two-letter site abbreviation that designates the physical location of the generated/stored waste (e.g., ID for Idaho National Laboratory [INL]). The site-specific letter designations for each of the sites are provided in Table 1. • A three-digit code that designates the physical and chemical form of the waste (e.g., content code 317 denotes TRU Metal Waste). For RH-TRU waste to be transported in the RH-TRU 72-B, the first number of this three-digit code is “3.” The second and third numbers of the three-digit code describe the physical and chemical form of the waste. Table 2 provides a brief description of each generic code. Content codes are further defined as subcodes by an alpha trailer after the three-digit code to allow segregation of wastes that differ in one or more parameter(s). For example, the alpha trailers of the subcodes ID 322A and ID 322B may be used to differentiate between waste packaging configurations. As detailed in the RH-TRAMPAC, compliance with flammable gas limits may be demonstrated through the evaluation of compliance with either a decay heat limit or flammable gas generation rate (FGGR) limit per container specified in approved content codes. As applicable, if a container meets the watt*year criteria specified by the RH-TRAMPAC, the decay heat limits based on the dose-dependent G value may be used as specified in an approved content code. If a site implements the administrative controls outlined in the RH-TRAMPAC and Appendix 2.4 of the RH-TRU Payload Appendices, the decay heat or FGGR

RE{sub 3}Au{sub 5}Zn (RE = Y, Sm, Gd-Ho). A new structure type with five- and six-membered rings as building units in a gold network

Energy Technology Data Exchange (ETDEWEB)

Gerke, Birgit; Poettgen, Rainer [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie and NRW Graduate School of Chemistry

2016-08-01

RE{sub 3}Au{sub 5}Zn (RE = Y, Sm, Gd-Ho) intermetallic compounds were synthesized by melting the elements in sealed tantalum tubes. They exhibit a new structure type which was studied by X-ray diffraction on powders and refined from single crystal diffraction data: Cmcm, a = 736.9(2), b = 1489.4(2), c = 1330.4(3) pm, wR2 = 0.0371, 1184 F{sup 2} values and 55 variables for Y{sub 3}Au{sub 4.92}Zn{sub 1.08} and a = 739.0(1), b = 1495.8(2), c = 1339.2(2) pm, wR2 = 0.0325, 1410 F{sup 2} values and 54 variables for Tb{sub 3}Au{sub 5}Zn. The network consists of five- and six-membered gold rings in puckered conformations. Atoms of the rare earth elements are placed within the cavities of this network where every third cavity is filled by a Zn{sub 2} dumbbell. The structure is discussed in detail and compared with the gold substructure of Hf{sub 7}Au{sub 10}.

Synthesis of nanocrystalline Zn0.5Mn0.5Fe2O4 via in situ polymerization technique

International Nuclear Information System (INIS)

Liu Xianming; Fu Shaoyun

2007-01-01

Nanocrystalline Zn 0.5 Mn 0.5 Fe 2 O 4 was synthesized through the pyrolysis of polyacrylate salt precursors prepared via in situ polymerization of the metal salts and acrylic acid. The pyrolysis behavior of the polymeric precursors was studied by use of thermal analysis. The as-obtained product was characterized by powder X-ray diffraction (XRD), transmission electron microscope (TEM), electron diffraction (ED) pattern, scanning electron microscopy (SEM) and electron dispersive X-ray (EDX) analysis. The results revealed that the particle size is in the range of 15-25 nm for Zn-Mn ferrites with good crystallinity. Magnetic properties of the sample at 300 K were measured using a vibrating sample magnetometer, which showed that the sample exhibited characteristics of superparamagnetism

No-carrier-added (NCA) synthesis of 6-[18F]fluoro-L-DOPA using 3,5,6,7,8,8a-hexahydro-7,7,8a-trimethyl-[6S-(6α, 8α, 8αβ)]-6,8-methano-2H-1,4-benzoxazin-2-one

International Nuclear Information System (INIS)

Horti, A.; Yale Univ., West Haven, CT; Redmond, D.E. Jr.; Soufer, R.

1995-01-01

3,5,6,7,8,8a-Hexahydro-7,7,8a-trimethyl-[6S-(6α,8α , 8αβ)]-6,8-methano-2H-1,4-benzoxazino-2-one (2) was investigated as chiral auxiliary for asymmetric NCA nucleophilic synthesis of 6-[ 18 F]Fluoro-L-DOPA. Direct condensation of 3,4-dimethoxy-2-[ 18 F]fluorobenzaldehyde (1a) or 6-[ 18 F]fluoro-piperonal (1b) in the presence of NaH with 2 gave the corresponding [ 18 F]-3-[(2-fluorophenyl)methylene]-3,5,6,7,8,8a-hexahydro-7,7,8 a-trimethyl-[6S-(3Z,3α,6α,8α,8αβ)]-6, 8-methano-2H-1,4-benzoxazin-2-one derivative 3a or 3b as a single stereoisomer. L-Selectride promoted hydrogenation of the olefinic double bond of these derivatives, in presence of tertbutyl alcohol, afforded the corresponding [ 18 F]-3-[(2-fluorophenyl) methyl]-3,5,6,7,8,8a-hexahydro-7,7,8a-trimethyl-[3S-(3α, 6α, 8α8αβ)]-6,8-methano-2H-1,4-benzoxazin-2-one derivatives (4a,b) without affecting the orientation of diasterofacial discrimination. Deprotection of the derivatives 4a,b yielded 6-[ 18 F]fluoro-L-DOPA (e.e. >90%, 3% radiochemical yield (EOB), total synthesis time 125 min, specific activity >2000 mCi/μmol). Direct deprotection/reduction of the compounds 3a,b provides the enantiomeric mixture of 6-[ 18 F]fluoro-D,L-DOPA (10-12% radiochemical yield) and, after chiral separation, 6-[ 18 F]fluoro-L-DOPA (e.e. 98%, 4-5% radiochemical yield). (author)

Neutron diffraction analysis of HRh[P(C6H5)3]4

International Nuclear Information System (INIS)

Bau, R.; Stevens, R.C.; McLean, M.; Koetzle, T.F.

1987-01-01

We have collected neutron diffraction data on a large single crystal of the title compound. The most surprising result is an extremely short Rh-H distance of 1.31(8) A, presumably caused by steric interactions involving the bulky triphenyl phosphine ligands. Crystallographic details: HRh[P(C 6 H 5 ) 3 ] 4 . 1 / 2 C 6 H 6 crystallizes in the space group Pa3, with a = b = c = 22.776(3) A, Z = 8. Data were collected at the Brookhaven High Flux Beam reactor at a temperature of -23 0 C, λ = 1.15882(7) A -1 . Least-squares refinement (in which the phenyl rings were treated as rigid groups) resulted in an R factor [based on data with f > 4σ(F)] of 0.12 for 914 reflections and 95 parameters. 10 refs

Determination of the half-life of sup 1 sup 0 sup 5 sup m Rh

CERN Document Server

Kronenberg, A K; Weber, R; Esterlund, R A; Patzelt, P

1998-01-01

Following a fast chemical separation of Ru isotopes from a fission-product mixture, sup 1 sup 0 sup 5 sup m Rh was periodically extracted from its precursor (4.44-h sup 1 sup 0 sup 5 Ru) for measurements of its half-life. The new value for the T sub 1 sub / sub 2 of sup 1 sup 0 sup 5 sup m Rh of (43.0+-0.3) s resolves the long-standing conflict in the literature between the two earlier measured values of 45 and 30 s.

Hydrothermal synthesis and characterization of a new three-dimensional hybrid zinc phosphate [Zn2(HPO4)2(4,4'-bipy)].3H2O with neutral porous framework

International Nuclear Information System (INIS)

Wang Lei; Yang Ming; Li Guanghua; Shi Zhan; Feng Shouhua

2006-01-01

Employing 4,4'-bipyridine as a bridged ligand, a new three-dimensional (3-D) hybrid zinc phosphate [Zn 2 (HPO 4 ) 2 (4,4'-bipy)].3H 2 O has been prepared under hydrothermal conditions and characterized by single crystal X-ray diffraction. This compound crystallizes in the monoclinic space group C2/c, with cell parameters, a=21.188(4)A, b=10.229(2)A, c=9.0656(18)A, β=90.21(3) o , V=1964.8(7)A 3 and Z=4. The connectivity of the ZnO 3 N and HPO 4 tetrahedra results in a 2-D neutral layer that with interesting 4,8 2 net along the bc plane. Furthermore, the 4,4'-bipyridine molecule links the 4,8 2 net into a 3-D structure. The water molecules sit in the middle of the channels and interact with the framework via hydrogen bonds. The compound exhibits intense photoluminescence at room temperature

Sulfonated graphene oxide-ZnO-Ag photocatalyst for fast photodegradation and disinfection under visible light.

Science.gov (United States)

Gao, Peng; Ng, Kokseng; Sun, Darren Delai

2013-11-15

Synthesis of efficient visible-light-driven photocatalyst is urgent but challenging for environmental remediation. In this work, for the first time, the hierarchical plasmonic sulfonated graphene oxide-ZnO-Ag (SGO-ZnO-Ag) composites were prepared through nanocrystal-seed-directed hydrothermal method combining with polyol-reduction process. The results indicated that SGO-ZnO-Ag exhibited much faster rate in photodegradation of Rhodamine B (RhB) and disinfection of Escherichia coli (E. coli), than ZnO, SGO-ZnO and ZnO-Ag. SGO-ZnO-Ag totally degraded RhB dye and kill 99% of E. coli within 20 min under visible light irradiation. The outstanding performances of SGO-ZnO-Ag were attributed to the synergetic merits of SGO sheets, ZnO nanorod arrays and Ag nanoparticles. Firstly, the light absorption ability of SGO-ZnO-Ag composite in the visible region was enhanced due to the surface plasmon resonance of Ag. In addition, the hierarchical structure of SGO-ZnO-Ag composite improved the incident light scattering and reflection. Furthermore, SGO sheets facilitated charge transfer and reduce electron-hole recombination rate. Finally, the tentative mechanism was proposed and verified by the photoluminescence (PL) measurement as well as the theoretical finite-difference time-domain (FDTD) simulation. In view of above, this work paves the way for preparation of multi-component plasmonic composites and highlights the potential applications of SGO-ZnO-Ag in photocatalytic wastewater treatment field. Crown Copyright © 2013. Published by Elsevier B.V. All rights reserved.

Superplastic forming of the Cd-17.4Zn alloy; Conformado superplastico de la aleacion Cd-17.4Zn

Energy Technology Data Exchange (ETDEWEB)

Llanes-Briceno, J. A.; Torres-Villasenor, G. [Universidad Nacional Autonoma de Mexico, Mexico, D.F. (Mexico)

2000-06-01

In the present work the necessary steps to carry on the superplastic forming of the Cd-17.4Zn alloy are defined. The use of either atmospheric pressure or gas pressure as forming tools is analyzed. The optimum values of the variable involved (temperature, maximum strain and sensitivity index) are determined while a method for the characterization of futures superplastic alloys is set forth. The experimental characterization of the superplastic forming is achieved with free bulging of circular membranes of 12, 16, 24, 32 and 40 mm in diameter and with three different membrane thicknesses (0.4, 0.6, 0.8 mm). [Spanish] Se definen los pasos necesarios para el conformado superplastico de la aleacion Cd-17.4 Zn. Se comparan la presion atmosferica y el gas a presion como herramientas de conformado. Se determinan los valores optimos de la variables involucradas (temperatura, deformacion maxima e indice de sensibilidad) y se plantea una metodologia para la caracterizacion de futuras aleaciones superplasticas. El conformado superplastico se caracteriza experimentalmente mediante el inflado libre de membranas circulares de 12, 16, 24, 32 y 40 mm de diametro y tres diferentes espesores (0.4, 0.6 y 0.8 mm). Se muestra la estructura perlitica (enfuiada al aive Cd-17.4Zn) y la estructura grano fino. Se muestra la profundidad de deformacion en tres espesores (0.4, 0.6, 0.8 mm) a P=200 Kpa y T = 200 y a T = 230.

Melatonin Inhibits GnRH-1, GnRH-3 and GnRH Receptor Expression in the Brain of the European Sea Bass, Dicentrarchus labrax

Directory of Open Access Journals (Sweden)

José Antonio Muñoz-Cueto

2013-04-01

Full Text Available Several evidences supported the existence of melatonin effects on reproductive system in fish. In order to investigate whether melatonin is involved in the modulation of GnRH systems in the European sea bass, we have injected melatonin (0.5 µg/g body mass in male specimens. The brain mRNA transcript levels of the three GnRH forms and the five GnRH receptors present in this species were determined by real time quantitative PCR. Our findings revealed day–night variations in the brain expression of GnRH-1, GnRH-3 and several GnRH receptors (dlGnRHR-II-1c, -2a, which exhibited higher transcript levels at mid-light compared to mid-dark phase of the photocycle. Moreover, an inhibitory effect of melatonin on the nocturnal expression of GnRH-1, GnRH-3, and GnRH receptors subtypes 1c, 2a and 2b was also demonstrated. Interestingly, the inhibitory effect of melatonin affected the expression of hypophysiotrophic GnRH forms and GnRH receptors that exhibit day–night fluctuations, suggesting that exogenous melatonin reinforce physiological mechanisms already established. These interactions between melatoninergic and GnRH systems could be mediating photoperiod effects on reproductive and other rhythmic physiological events in the European sea bass.

A re-evaluation of k0 and related nuclear data for the 555.8 keV gamma-line emitted by the 104mRh-104Rh mother-daughter pair for use in NAA

International Nuclear Information System (INIS)

Corte, Frans de; Lierde, Stijn van; Simonits, Andras; Bossus, Danieel; Sluijs, Robbert van; Pomme, Stefaan

1999-01-01

A re-evaluation is made of the k 0 -factor and related nuclear data for the 555.8 keV gamma-ray of the 104m Rh- 104 Rh mother-daughter pair that are important in neutron activation analysis (NAA). This study considers that the relevant level is also fed by the 4.34 min 104m Rh mother (with an absolute gamma-ray emission probability γ 2 =0.13%) and not only, as assumed in former work, by the 42.3 s 104 Rh daughter isotope (with γ 3 =2.0%). In view of this, generalised equations were developed for both the experimental determination and the analytical use of the k 0 -factor and of the associated parameters k 0 (m)/k 0 (g), Q 0 (m) and Q 0 (g) [(m): 104m Rh; (g): 104 Rh], requiring the introduction of the γ 2 and γ 3 data and also of the 104m Rh→ 104 Rh fractional decay factor F 2 (=0.9987). The experimental determinations were based on irradiations performed in the BR1 reactor in Mol and the WWR-M reactor in Budapest. Furthermore, considering the special formation of the 555.8 keV gamma-ray, the procedure for true-coincidence correction was revised as well. All this led to the compilation and recommendation of a new set of 'k 0 -NAA' data

Miniaturized printed K shaped monopole antenna with truncated ground plane for 2.4/5.2/5.5/5.8 wireless lan applications

Science.gov (United States)

Chandan, Bharti, Gagandeep; Srivastava, Toolika; Rai, B. S.

2018-04-01

A novel truncated ground plane monopole antenna is proposed for wide band wireless local area network (WLAN) applications. The antenna contains a rectangular patch with a rectangular ring, a circular slot and a truncated ground plane printed on opposite sides of a low cost substrate FR4. The operating frequency bands for the antenna are band1 (2.4-2.88 GHz) and band 2 (4.8-6.3 GHz) with ≤ - 10 dB return loss which covers 2.4/5.2/5.5/5.8 GHz WLAN bands. The antenna is compact with overall dimension 26×40×0.8 mmł and with the dimension of patch 16×16×0.8 mm3. The two bands of antenna is obtained by cutting a rectangular ring and a circular slot in the patch and return loss is improved by cutting two rectangular slot in the ground plane. Performance measures of the antenna are shown in terms of return loss, current distribution, radiation pattern and gain. To verify the simulated results, the antenna is also fabricated and tested. The simulated and fabricated results have been found in good agreement.

Facile preparation of well-combined lignin-based carbon/ZnO hybrid composite with excellent photocatalytic activity

Science.gov (United States)

Wang, Huan; Qiu, Xueqing; Liu, Weifeng; Yang, Dongjie

2017-12-01

In this work, a novel lignin-based carbon/ZnO (LC/ZnO) hybrid composite with excellent photocatalytic performance was prepared through a convenient and environment friendly method using alkali lignin (AL) as carbon source. The morphological, microstructure and optical properties of the as-prepared LC/ZnO hybrid composite was characterized with scanning electron microscope (SEM), X-ray diffraction (XRD), Raman and UV-vis. The resulting LC/ZnO hybrid is composed of highly dispersed ZnO nanoparticles embedded on a lignin-based carbon nanosheet, showing excellent photogenerated electrons and holes separation and migration efficiency. The photocatalytic activity of LC/ZnO was much higher than the pure ZnO. The LC/ZnO hybrid composite showed different photocatalytic mechanism for degradation of negative methyl orange (MO) and positive Rhodamine B (RhB). It showed that h+ was the main photocatalytic active group during the degradation of MO, ·O2- and ·OH were the photocatalytic active groups during degradation of RhB. This reported photocatalyst with selective degradation of positive and negative organic dyes may have a great application prospect for photoelectric conversion and catalytic materials. Results of this work were of practical importance for high-valued utilization of lignin for carbon materials.

Improving the catalytic activity of magnetic Fe3O4/ZnO-CdO/reduced graphene oxide for ultrasonic degradation of the organic pollutants and the green oxidation of olefins

Science.gov (United States)

Mirzazadeh, Hoda; Lashanizadegan, Maryam

2018-05-01

Magnetic Fe3O4/ZnO-CdO/reduced graphene oxide (MFZC/RGO) has been synthesized by simple hydrothermal method. The structure and morphology were investigated by X-ray diffraction (XRD), Transmission electron microscopy (TEM), Scanning electron microscopy (SEM), Energy-dispersive X-ray spectroscopy (EDS), Diffuse reflectance spectroscopy (DRS), Vibrating sample magnetometer (VSM), Raman and Fourier-transform infrared spectroscopy (FTIR). MFZC/RGO was applied as catalyst in degradation of methylene blue (MB), rhodamin B (RhB) and methylorange (MO) under ultrasonic irradiation. Based on the results, excellent degradation efficiencies of MB, RhB and MO (>99%) were achieved within 10, 20 and 20 min, respectively under oxygen flow. Moreover the catalytic property of MFZC/RGO was investigated in oxidation of styrene, α-methyl styrene, cyclohexene and cyclooctene under oxygen flow. In addition, MFZC/RGO can be easily collected and separated by an external magnet. The catalyst displayed negligible loss in activity and selectivity within several successive runs due to super paramagnetism.

Absence of a long-range ordered magnetic ground state in Pr3Rh4Sn13 studied through specific heat and inelastic neutron scattering

Science.gov (United States)

Nair, Harikrishnan S.; Ogunbunmi, Michael O.; Ghosh, S. K.; Adroja, D. T.; Koza, M. M.; Guidi, T.; Strydom, A. M.

2018-04-01

Signatures of absence of a long-range ordered magnetic ground state down to 0.36 K are observed in magnetic susceptibility, specific heat, thermal/electrical transport and inelastic neutron scattering data of the quasi-skutterudite compound Pr3Rh4Sn13 which crystallizes in the Yb3Rh4Sn13-type structure with a cage-like network of Sn atoms. In this structure, Pr3+ occupies a lattice site with D 2d point symmetry having a ninefold degeneracy corresponding to J  =  4. The magnetic susceptibility of Pr3Rh4Sn13 shows only a weak temperature dependence below 10 K otherwise remaining paramagnetic-like in the range, 10 K-300 K. From the inelastic neutron scattering intensity of Pr3Rh4Sn13 recorded at different temperatures, we identify excitations at 4.5(7) K, 5.42(6) K, 10.77(5) K, 27.27(5) K, 192.28(4) K and 308.33(3) K through a careful peak analysis. However, no signatures of long-range magnetic order are observed in the neutron data down to 1.5 K, which is also confirmed by the specific heat data down to 0.36 K. A broad Schottky-like peak is recovered for the magnetic part of the specific heat, C 4f, which suggests the role of crystal electric fields of Pr3+ . A crystalline electric field model consisting of 7 levels was applied to C 4f which leads to the estimation of energy levels at 4.48(2) K, 6.94(4) K, 11.23(8) K, 27.01(5) K, 193.12(6) K and 367.30(2) K. The CEF energy levels estimated from the heat capacity analysis are in close agreement with the excitation energies seen in the neutron data. The Sommerfeld coefficient estimated from the analysis of magnetic specific heat is γ = 761(6) mJ K-2 mol-Pr which suggests the formation of heavy itinerant quasi-particles in Pr3Rh4Sn13. Combining inelastic neutron scattering results, analysis of the specific heat data down to 0.36 K, magnetic susceptibility and, electrical and thermal transport, we establish the absence of long-range ordered magnetic ground state in Pr3Rh4Sn13.

High hard magnetic properties and cellular structure of nanocomposite magnet Nd4.5Fe73.8B18.5Cr0.5Co1.5Nb1Cu0.2

International Nuclear Information System (INIS)

The, N.D.; Chau, N.; Vuong, N.V.; Quyen, N.H.

2006-01-01

The formation of special nanostructure, cellular structure, in Nd 4.5 Fe 73.8 B 18.5 Cr 0.5 Co 1.5 Nb 1 Cu 0.2 nanocomposite magnet has been observed by means of SEM for the first time. Ultrafine structure of cellules with thickness of 20-25 nm and length in range of 200-300 nm leads to high shape anisotropy of the materials. Therefore, high hard magnetic properties were obtained with (BH) max up to 17.3 MG Oe in ribbons with very high remanence of 13.5 kG. The role of Cr and Co in the formation and refinement of cellular structure is proposed. Effect of heat treatment on hard magnetic properties is discussed in detail

Structural, optical, photoluminescence and photocatalytic assessment of Sr-doped ZnO nanoparticles

International Nuclear Information System (INIS)

Pradeev Raj, K.; Sadaiyandi, K.; Kennedy, A.; Thamizselvi, R.

2016-01-01

ZnO nanoparticles (NPs) and Strontium doped ZnO nanoparticles (2–6 mol %) (SZ-NPs) were synthesized via Co-precipitation method. Synthesized samples were investigated by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), Elemental dispersive spectroscopy (EDS), UV–visible, and Photoluminescence (PL) spectroscopy. Photocatalytic studies for Rhodamine B (RhB) dye in aqueous solution under UV–Vis radiation. XRD analysis confirms that all the samples have hexagonal wurtzite structure. The average crystallite size of the nanoparticles was in the range of 29–51 nm. From the Williamson –Hall (W-H) plot, a positive slope is inferred for pure and SZ-NPs, confirming the presence of tensile strain. SEM images reveal the synthesized NPs are in nanometer range with various shapes are observed. The presence of strontium (Sr) in the host lattice was confirmed by EDS spectroscopy. The optical analysis shows the absorption decreases on doping and shifts slightly towards the longer wavelength region. The band gap energy (Eg) decreases (3.32–3.03 eV) with the increase of Sr dopant concentration. The photoluminescence (PL) spectrum reveals the UV emission is strong near the band-edge region (NBE) (392 nm) and intrinsic defects resulted in series of Vis emissions around 400–560 nm. Kinetic studies on RhB dye indicates the degradation rate has increased with dopant concentration. The improved photocatalytic activity is observed due to the efficient charge separation, improved visible light absorption, inhibition of the electron-hole pair's recombination and better adsorptive of RhB dye molecule on the surface of SZ-NPs. Moreover, the reduction in the total organic carbon (TOC) results reveals the improved photocatalytic activity of strontium doped ZnO NPs. - Highlights: • Effective synthesis of ZnO and Sr−ZnO nanoparticles by co-precipitation method. • Samples were characterized by XRD, SEM, EDS, UV–Vis and PL technique. • Higher optical absorption and

Structural, optical, photoluminescence and photocatalytic assessment of Sr-doped ZnO nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Pradeev Raj, K., E-mail: pradeevraj@gmail.com [Research and Development Centre, Bharathiar University, Coimbatore, 641 046, Tamilnadu (India); Department of Physics, CSI College of Engineering, Ooty, The Nilgiris, 643 215, Tamil Nadu (India); Sadaiyandi, K. [Department of Physics, Alagappa Government Arts College, Karaikudi, Sivagangai, 630 003, Tamil Nadu (India); Kennedy, A. [Department of Physics, CSI College of Engineering, Ooty, The Nilgiris, 643 215, Tamil Nadu (India); Thamizselvi, R. [Department of Chemistry, L.R.G. Govt Arts College for Women, Tirupur, 641604, Tamil Nadu (India)

2016-11-01

ZnO nanoparticles (NPs) and Strontium doped ZnO nanoparticles (2–6 mol %) (SZ-NPs) were synthesized via Co-precipitation method. Synthesized samples were investigated by X-ray diffraction (XRD), Scanning Electron Microscopy (SEM), Elemental dispersive spectroscopy (EDS), UV–visible, and Photoluminescence (PL) spectroscopy. Photocatalytic studies for Rhodamine B (RhB) dye in aqueous solution under UV–Vis radiation. XRD analysis confirms that all the samples have hexagonal wurtzite structure. The average crystallite size of the nanoparticles was in the range of 29–51 nm. From the Williamson –Hall (W-H) plot, a positive slope is inferred for pure and SZ-NPs, confirming the presence of tensile strain. SEM images reveal the synthesized NPs are in nanometer range with various shapes are observed. The presence of strontium (Sr) in the host lattice was confirmed by EDS spectroscopy. The optical analysis shows the absorption decreases on doping and shifts slightly towards the longer wavelength region. The band gap energy (Eg) decreases (3.32–3.03 eV) with the increase of Sr dopant concentration. The photoluminescence (PL) spectrum reveals the UV emission is strong near the band-edge region (NBE) (392 nm) and intrinsic defects resulted in series of Vis emissions around 400–560 nm. Kinetic studies on RhB dye indicates the degradation rate has increased with dopant concentration. The improved photocatalytic activity is observed due to the efficient charge separation, improved visible light absorption, inhibition of the electron-hole pair's recombination and better adsorptive of RhB dye molecule on the surface of SZ-NPs. Moreover, the reduction in the total organic carbon (TOC) results reveals the improved photocatalytic activity of strontium doped ZnO NPs. - Highlights: • Effective synthesis of ZnO and Sr−ZnO nanoparticles by co-precipitation method. • Samples were characterized by XRD, SEM, EDS, UV–Vis and PL technique. • Higher optical absorption

THE DECEPTIVELY SIMPLE THERMOLYSIS OF TRIVALENT PERMETHYLTITANOCENE DERIVATIVES (ETA-5-C5ME5)2TIR - FORMATION OF A TETRAMETHYLFULVENE TITANIUM COMPOUND (ETA-6-C5ME4CH2)(ETA-5-C5ME5)TI AND RH, CATALYZED BY PERMETHYLTITANOCENE HYDRIDE, (ETA-5-C5ME5)2TIH

NARCIS (Netherlands)

LUINSTRA, GA; TEUBEN, JH

1992-01-01

The complexes Cp*2TiR (Cp* = eta-5-C5Me5; R = Me, Et, n-Pr, C2H3, CH2CMe3, Ph) undergo thermolysis to yield the fulvene complex Cp*FvTi (Fv = eta-6-C5Me4CH2) and RH. Kinetic measurements and deuterium labeling studies show that the decomposition is catalyzed by Cp*2TiH, which is formed either by

Syntheses and characterization of two new zinc phosphites with 1D chains decorated by Zn-centered complexes

Science.gov (United States)

Zhong, You-Ju; Chen, Yong-Mei; Sun, Yan-Qiong; Yang, Guo-Yu

2005-09-01

Two inorganic-organic hybrid solids, Zn 2(phen)(HPO 3) 2 ( 1) and Zn(phen)(HPO 3) ( 2), have been synthesized under solvothermal conditions in the presence of 1,10-phenanthroline (phen) ligands. Their structures were determined by single-crystal X-ray diffraction and further characterized by FTIR, elemental analysis, powder X-ray diffraction, thermogravimetric analysis and fluorescent spectra. Compound 1 crystallizes in the triclnic system, space group P-1, a=8.1813(3) Å, b=8.5535(3) Å, c=12.3031(5) Å, α=75.609(1)°, β=79.145(2)°, γ=67.157(2)°, V=764.46(5) Å3, Z=2. Compound 2 is monoclinic, C2/c, a=16.1044(7) Å, b=18.9447(6) Å, c=8.1713(6) Å, β=94.175(4)°, V=2486.4(2) Å3, Z=8. Both structures consist of 1D chains constructed from strictly alternating ZnO 4 and HPO 3 polyhedra through sharing vertices. The chains are further decorated by Zn-centered complex architectures, [Zn(phen)] 2+ for 1 and [Zn(phen) 2] 2+ for 2. The 2D and 3D supramolecular arrays for 1 and 2 are stably stacked via strong π- π interactions of the phen groups, respectively.

Syntheses and characterization of two new zinc phosphites with 1D chains decorated by Zn-centered complexes

International Nuclear Information System (INIS)

Zhong Youju; Chen Yongmei; Sun Yanqiong; Yang Guoyu

2005-01-01

Two inorganic-organic hybrid solids, Zn 2 (phen)(HPO 3 ) 2 (1) and Zn(phen)(HPO 3 ) (2), have been synthesized under solvothermal conditions in the presence of 1,10-phenanthroline (phen) ligands. Their structures were determined by single-crystal X-ray diffraction and further characterized by FTIR, elemental analysis, powder X-ray diffraction, thermogravimetric analysis and fluorescent spectra. Compound 1 crystallizes in the triclnic system, space group P-1, a=8.1813(3)A, b=8.5535(3)A, c=12.3031(5)A, α=75.609(1) o , β=79.145(2) o , γ=67.157(2) o , V=764.46(5)A 3 , Z=2. Compound 2 is monoclinic, C2/c, a=16.1044(7)A, b=18.9447(6)A, c=8.1713(6)A, β=94.175(4) o , V=2486.4(2)A 3 , Z=8. Both structures consist of 1D chains constructed from strictly alternating ZnO 4 and HPO 3 polyhedra through sharing vertices. The chains are further decorated by Zn-centered complex architectures, [Zn(phen)] 2+ for 1 and [Zn(phen) 2 ] 2+ for 2. The 2D and 3D supramolecular arrays for 1 and 2 are stably stacked via strong π-π interactions of the phen groups, respectively

Ovarian ablation in the adjuvant treatment of breast cancer: GnRH-analogues, ovarectomy or radiocastration - 'The philosopher's stone' instead of 'Chamber of secrets'?; Ovarielle Suppression in der adjuvanten Therapie des Mammakarzinoms: GnRH-Analoga, Ovarektomie oder Radiomenolyse - 'Stein der Weisen' statt 'Kammer des Schreckens'?

Energy Technology Data Exchange (ETDEWEB)

Hoffmann, W.; Schiebe, M. [Staedtisches Klinikum Braunschweig (Germany); Seegenschmiedt, H. [Alfried-Krupp-Krankenhaus, Essen (Germany)

2002-08-01

Background: Ovarian suppression in the adjuvant treatment of perimenopausal women with breast cancer is an important option. The therapeutic goal can be accomplished by administration of GnRH-analogues, ovarectomy or radiocastration. Patients and methods: We describe the advantages and the therapy related side effects and compare the different treatment modalities with each other. Results: Because of its reversibility and patients' compliance GnRH-analogues seem to be advantageous especially in younger premenopausal women. When longer term side effects of artificially induced menopause are less important, therapeutic alternatives such as radiocastration or ovarectomy are effective without obvious superiority between these options. Conclusion: Even in the background of the increasing use of GnRH-analogues radiocastration remains still a therapeutic alternative because of its cost-effectiveness and feasibility. This accounts especially for peri- or premenopausal women above the age of 45. (orig.) [German] Hintergrund: Bei praemenopausalen Patienten mit rezeptorpositiven Mammakarzinomen stellt die ovarielle Suppression einen wichtigen Schritt in der adjuvanten Therapie dar. Neben den GnRH-Analoga kommen hierfuer die Ovarektomie oder die Radiomenolyse infrage. Patienten und Methode: Die vorliegende Arbeit stellt die Vorteile der einzelnen Therapieoptionen den therapiebedingten Nebenwirkungen gegenueber und vergleicht die Methoden untereinander. Ergebnisse: Wegen der Reversibilitaet und der Patientenakzeptanz sollten GnRH-Analoga besonders bei juengeren praemenopausalen Patientinnen angewendet werden. In der Differentialtherapie von Patientinnen, bei denen die Langzeitnebenwirkungen einer iatrogen induzierten Menopause weniger zu befuerchten sind, kommen auch die anderen Verfahren in Betracht. Hierbei stehen Radiomenolyse und Ovarektomie gleichwertig nebeneinander. Schlussfolgerung: Die differentialtherapeutische Entscheidung zu einer der Methoden sollte

Uniform Fe3O4 coating on flower-like ZnO nanostructures by atomic layer deposition for electromagnetic wave absorption.

Science.gov (United States)

Wan, Gengping; Wang, Guizhen; Huang, Xianqin; Zhao, Haonan; Li, Xinyue; Wang, Kan; Yu, Lei; Peng, Xiange; Qin, Yong

2015-11-21

An elegant atomic layer deposition (ALD) method has been employed for controllable preparation of a uniform Fe3O4-coated ZnO (ZnO@Fe3O4) core-shell flower-like nanostructure. The Fe3O4 coating thickness of the ZnO@Fe3O4 nanostructure can be tuned by varying the cycle number of ALD Fe2O3. When serving as additives for microwave absorption, the ZnO@Fe3O4-paraffin composites exhibit a higher absorption capacity than the ZnO-paraffin composites. For ZnO@500-Fe3O4, the effective absorption bandwidth below -10 dB can reach 5.2 GHz and the RL values below -20 dB also cover a wide frequency range of 11.6-14.2 GHz when the coating thickness is 2.3 mm, suggesting its potential application in the treatment of the electromagnetic pollution problem. On the basis of experimental observations, a mechanism has been proposed to understand the enhanced microwave absorption properties of the ZnO@Fe3O4 composites.

Synthesis of (±)-8-deisopropyladunctin B.

Science.gov (United States)

Nomura, Sayo; Arimitsu, Kenji; Yamaguchi, Satoshi; Kosuga, Yuya; Kakimoto, Yuko; Komai, Takanori; Hasegawa, Kazumasa; Nakanishi, Akira; Miyoshi, Tamami; Iwasaki, Hiroki; Ozeki, Minoru; Kawasaki, Ikuo; Kurume, Ai; Ohta, Shunsaku; Yamashita, Masayuki

2012-01-01

(±)-8-Deisopropyladunctin B, the deisopropyl form of adunctin B, which was isolated from the leaves of Piper aduncum (Piperaceae) collected in Papua New Guinea, was synthesized in 0.77% overall yield in 17 steps from 5,7-dimethoxycoumarin-3-carboxylate. The key step was our original stereoconvergent skeleton transformation from 1,2,2a,8b-tetrahydro-3H-benzo[b]cyclobuta[d]pyran-3-one to 1,2,4a,9b-tetrahydrodibenzofuran-4-ol with dimethylsulfoxonium methylide.

5-Methyl-4-oxo-4,6-dihydro-3H-pyridazino[4,5-b]carbazole-1-carbonitrile

Directory of Open Access Journals (Sweden)

Norbert Haider

2010-02-01

Full Text Available The title compound was prepared in excellent yield from 5-methyl-4-oxo-4,6-dihydro-3H-pyridazino[4,5-b]carbazole-1-carbaldehyde by treatment with hydroxylamine hydrochloride in formic acid without isolation of the intermediate oxime.

Effect of 120 MeV 28Si9+ ion irradiation on structural and magnetic properties of NiFe2O4 and Ni0.5Zn0.5Fe2O4

Science.gov (United States)

Sharma, R.; Raghuvanshi, S.; Satalkar, M.; Kane, S. N.; Tatarchuk, T. R.; Mazaleyrat, F.

2018-05-01

NiFe2O4, Ni0.5Zn0.5Fe2O4 samples were synthesized using sol-gel auto combustion method, and irradiated by using 120 MeV 28Si9+ ion with ion fluence of 1×1012 ions/cm2. Characterization of pristine, irradiated samples were done using X-Ray Diffraction (XRD), Field Emission Scanning Microscopy (FE-SEM), Energy Dispersive X-ray Analysis (EDAX) and Vibrating Sample Magnetometer (VSM). XRD validates the single phase nature of pristine, irradiated Ni- Zn nano ferrite except for Ni ferrite (pristine, irradiated) where secondary phases of α-Fe2O3 and Ni is observed. FE- SEM images of pristine Ni, Ni-Zn ferrite show inhomogeneous nano-range particle size distribution. Presence of diamagnetic ion (Zn2+) in NiFe2O4 increases oxygen positional parameter (u 4¯3m ), experimental, theoretical saturation magnetization (Msexp., Msth.), while decreases the grain size (Ds) and coercivity (Hc). With irradiation Msexp., Msth. increases but not much change are observed in Hc. New antistructure modeling for the pristine, irradiated Ni and Ni-Zn ferrite samples was used for describing the surface active centers.

Cobalt(II), nickel(II), copper(II), and zinc(II) complexes with [3(5)]adamanzane, 1,5,9,13-tetraazabicyclo[7.7.3]nonadecane and [(2.3)(2).2(1)]adamanzane, 1,5,9,12-tetraazabicyclo[7.5.2]hexadecane

DEFF Research Database (Denmark)

Broge, Louise; Pretzmann, Ulla; Jensen, Nicolai

2001-01-01

) and of three cobalt(II), four nickel(II), one copper(II), and two zinc(II) complexes with [3(5)]adamanzane. For nine of these compounds (2-8, 10b, and 12) the single-crystal X-ray structures were determined. The coordination geometry around the metal ion is square pyramidal in [Cu([(2.3)(2).2(1)]adz)Br]ClO4 (2......) and trigonal bipyramidal in the isostructural structures [Cu([3(5)]adz)Br]Br (3), [Ni-([3(5)]adz)Cl]Cl (5), [Ni([3(5)]adz)Br]Br (6), and [Co([3(5)]adz)Cl]Cl (8). In [Ni([3(5)]adz)(NO3)]NO3 (4) and [Ni([3(5)]-adz)(ClO4)]ClO4 (7) the coordination geometry around nickel(II) is a distorted octahedron...... with the inorganic ligands at cis positions. The coordination polyhedron around the metal ion in [Co([3(5)]adz)][ZnCl4] (10b) and [Zn([3(5)]adz)][ZnCl4] (12) is a slightly distorted tetrahedron. Anation equilibrium constants were determined spectrophotometrically for complexes 2-6 at 25 and 40 degreesC and fall...