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Sample records for ni ii emission

  1. and ni(ii)

    African Journals Online (AJOL)

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    NI(II) COMPLEXES WITH SCHIFF BASE DERIVED FROM SULPHANILAMINE AND. SALICYLALDEHYDE. ⃰Siraj, I. T. and ... with nickel(II) and cobalt(II) chloride in 2:1 mole ratio yielded Ni(II) and Co(II) complexes respectively. The synthesized .... coordinated ligand (coordination number) was determined using the relation ...

  2. Co(II), Ni(II) and Zn(II)

    Indian Academy of Sciences (India)

    Unknown

    161. Synthesis, characterisation and electrochemical behaviour of. Cu(II), Co(II), Ni(II) and Zn(II) complexes derived from acetylacetone and p-anisidine and their antimicrobial activity. N RAMAN*, V MUTHURAJ, S RAVICHANDRAN and. A KULANDAISAMY. Department of Chemistry, VHNSN College, Virudhunagar 626 001 ...

  3. Synthesis and characterisation of Cu (II), Ni (II), Mn (II), Zn (II) and ...

    Indian Academy of Sciences (India)

    Home; Journals; Journal of Chemical Sciences; Volume 113; Issue 3. Synthesis and characterisation of Cu(II), Ni(II), Mn(II), Zn(II) and VO(II) Schiff base complexes derived from o-phenylenediamine and acetoacetanilide. N Raman Y Pitchaikani Raja A Kulandaisamy. Inorganic Volume 113 Issue 3 June 2001 pp 183-189 ...

  4. Ni (II) complexes of dithiophosphonic acids

    Indian Academy of Sciences (India)

    Home; Journals; Journal of Chemical Sciences; Volume 126; Issue 4. Ni(II) complexes of dithiophosphonic acids ... Gholivand Ali Asghar Ebrahimi Valmoozi. Volume 126 Issue 4 July 2014 pp 1125-1133 ... The new compounds were additionally tested in view of their anti-bacterial properties. The ligands containing amine ...

  5. Synthesis and characterisation of Cu(II), Ni(II), Mn(II), Zn(II) and VO(II ...

    Indian Academy of Sciences (India)

    Unknown

    Synthesis and characterisation of Cu(II), Ni(II), Mn(II), Zn(II) and VO(II) Schiff base complexes derived from o-phenylenediamine and acetoacetanilide. N RAMAN*, Y PITCHAIKANI RAJA and A KULANDAISAMY. Department of Chemistry, VHNSN College, Virudhunagar 626 001, India e-mail: ra_man@123india.com.

  6. Structural alteration of hexagonal birnessite by aqueous Mn(II): Impacts on Ni(II) sorption

    Energy Technology Data Exchange (ETDEWEB)

    Lefkowitz, Joshua P.; Elzinga, Evert J.

    2017-09-01

    We studied the impacts of aqueous Mn(II) (1 mM) on the sorption of Ni(II) (200 μM) by hexagonal birnessite (0.1 g L- 1) at pH 6.5 and 7.5 with batch experiments and XRD, ATR-FTIR and Ni K-edge EXAFS analyses. In the absence of Mn(II)aq, sorbed Ni(II) was coordinated predominantly as triple corner-sharing complexes at layer vacancies at both pH values. Introduction of Mn(II)aq into Ni(II)-birnessite suspensions at pH 6.5 caused Ni(II) desorption and led to the formation of edge-sharing Ni(II) complexes. This was attributed to competitive displacement of Ni(II) from layer vacancies by either Mn(II) or by Mn(III) formed through interfacial Mn(II)-Mn(IV) comproportionation, and/or incorporation of Ni(II) into the birnessite lattice promoted by Mn(II)-catalyzed recrystallization of the sorbent. Similar to Mn(II)aq, the presence of HEPES or MES caused the formation of edge-sharing Ni(II) sorption complexes in Ni(II)-birnessite suspensions, which was attributed to partial reduction of the sorbent by the buffers. At pH 7.5, interaction with aqueous Mn(II) caused reductive transformation of birnessite into secondary feitknechtite that incorporated Ni(II), enhancing removal of Ni(II) from solution. These results demonstrate that reductive alteration of phyllomanganates may significantly affect the speciation and solubility of Ni(II) in anoxic and suboxic environments.

  7. Fe(II), Ni(II), Ru(II)

    Indian Academy of Sciences (India)

    Administrator

    Ru(II) and Os(II) complexes of modified phenanthroline ligands. C V SASTRI, D EASWARAMOORTHY #, ATHILAKSHMI #,. L GIRIBABU and B G MAIYA. School of Chemistry, University of Hyderabad, Hyderabad 500 046, India. #Present address: Crescent Engineering College, Vandalur, Chennai 600 048,. India.

  8. REMOVAL OF Ni(II) FROM AQUEOUS SOLUTION USING LEAF ...

    African Journals Online (AJOL)

    Preferred Customer

    ABSTRACT. The present study investigates the possibility of using leaf, bark and seed of Moringa stenopetala as alternative adsorbents for removal of Ni(II) from aqueous solutions. The optimum adsorption conditions for removal of Ni(II) were found to be 30, 20 and 50 mg/L initial concentration, 1.5, 2 and 2.5 g adsorbent ...

  9. Hydride Reactivity of Ni-II-X-Ni-II Entities : Mixed-Valent Hydrido Complexes and Reversible Metal Reduction

    NARCIS (Netherlands)

    Gehring, Henrike; Metzinger, Ramona; Herwig, Christian; Intemann, Julia; Harder, Sjoerd; Limberg, Christian

    After the lithiation of PYR-H2 (PYR2-=[{NC(Me)C(H)C(Me)NC6H3(iPr)2}2(C5H3N)]2-), which is the precursor of an expanded beta-diketiminato ligand system with two binding pockets, its reaction with [NiBr2(dme)] led to a dinuclear nickel(II)bromide complex, [(PYR)Ni(mu-Br)NiBr] (1). The bridging bromide

  10. Optimal synthesis of a Ni(II)-dimethylglyoxime ion-imprinted polymer ...

    African Journals Online (AJOL)

    A Ni(II)-dimethylglyoxime ion-imprinted polymer {Ni(II)-DMG IIP} was optimised by the uniform design experimental method and used to adsorb Ni(II) ions from ... The optimal molar ratios of crosslinker to monomer, monomer to template and nickel(II) sulphate hexahydrate (NiSO4.6H2O) to 4-vinylpyridine to dimethylglyoxime ...

  11. Micellar effect on metal-ligand complexes of Co(II), Ni(II), Cu(II) and ...

    African Journals Online (AJOL)

    Chemical speciation of citric acid complexes of Co(II), Ni(II), Cu(II) and Zn(II) was investigated pH-metrically in 0.0-2.5% anionic, cationic and neutral micellar media. The primary alkalimetric data were pruned with SCPHD program. The existence of different binary species was established from modeling studies using the ...

  12. Chemical speciation of L-glutamine complexes with Co(II), Ni(II) and ...

    African Journals Online (AJOL)

    The impact of cationic micelles on the protonation equilibria of L-glutamine and chemical speciation of its complexes with Co(II), Ni(II) and Cu(II) have been studied by monitoring hydrogen ion concentration pH metrically at 303 K and at an ionic strength of 0.16 M. The protonation constants and binary stability constants ...

  13. Sequestration of Cu(II), Ni(II), and Co(II) by ethyleneimine immobilized on silica

    International Nuclear Information System (INIS)

    Arakaki, Luiza N.H.; Alves, Ana Paula M.; Silva Filho, Edson C. da; Fonseca, Maria G.; Oliveira, Severino F.; Espinola, Jose Geraldo P.; Airoldi, Claudio

    2007-01-01

    Thermodynamic data on interaction of Cu(II), Ni(II), and Co(II) with silica modified with ethyleneimine are obtained by calorimetric titration. The amount of ethyleneimine anchored on silica surface was estimated to be 0.70 mmol g -1 . The enthalpies of binding Ni(II), Cu(II) and Co(II), are -3.59 ± 0.001, -4.88 ± 0.001, and -7.75 ± 0.003 kJ mol -1 , respectively

  14. Studies of Ni(II) & Cu(II) complexes with ampicillin | Guru | Nigerian ...

    African Journals Online (AJOL)

    Ni(II) and Cu(II) complex with ampicillin have been synthesized and characterized. On the basis of elemental analysis and molar conductance, formulas Ni(C16H19 N3O4S)MoO4H2O and Cu(C16H19N3O4S)MoO4H2O have been suggested for the complexes under study. The geometries of the complexes have been ...

  15. Synthesis, crystal structure and catecholase activity of a Ni (II ...

    Indian Academy of Sciences (India)

    Home; Journals; Journal of Chemical Sciences; Volume 126; Issue 6. Synthesis, crystal structure and catecholase activity of a Ni(II) complex derived from a tetradentate Schiff base ligand. Pradipta Kumar Basu Merry Mitra Amrita Ghosh Latibuddin Thander Chia -Her Lin Rajarshi Ghosh. Rapid Communications Volume 126 ...

  16. Ni(II) decorated nano silicoaluminophosphate molecular sieves ...

    Indian Academy of Sciences (India)

    the modified carbon paste electrode was prepared by nano SAPO molecular sieves and nickel (II) ion incorporated at this electrode. The electrochemical behaviour of the modified electrode (Ni-SAPO/CPE) towards the oxidation of methanol was investigated by cyclic voltammetry and chronoamperometry methods.

  17. and ni (ii) complexes with n

    African Journals Online (AJOL)

    DR. AMINU

    68.06KJmol-1, respectively. The ratio of metal ion to Schiff base determined potentiometrically and spectrophotometrically for the complex compounds is 1: 2. The IR spectrum of the Schiff base shows bands observable in the two Schiff base complex compounds, indicating the coordination of the Schiff base to the cobalt(II) ...

  18. Phosphonate Modified Silica for Adsorption of Co(II, Ni(II, Cu(II, and Zn(II

    Directory of Open Access Journals (Sweden)

    Dian Maruto Widjonarko

    2014-07-01

    Full Text Available A new phosphonate modified silica (PMS has been investigated for adsorption of Co(II, Ni(II, Cu(II, and Zn(II in aqueous solution. The adsorbent was modified of silica by immobilizing aminoethyl dihydrogen phosphate (AEPH2 on 1,4-dibromobutane grafted silica. The physicochemical of the adsorbent was investigated using Fourier Transform Infra-red (FTIR spectroscopy, X-ray Fluorescence (XRF, and N2 gas adsorption/desorption. The adsorption study was carried out in a batch system by mixing solution of metal ions at various pHs, contact times, and initial metal ion concentrations. The unadsorbed metals were determined by Flame Atomic Absorption Spectrophotometry (FAAS. Result of characterization showed that PMS has been successfully prepared. The product contained 45.99% (w/w silica and 1.33% (w/w phosphorous with surface area, pore volume, and pore size of 115.3 m2g-1; 0.7578 mLg-1; and 131.44 Å, respectively. Adsorption of metal ions on PMS occurred quite fast, less than 30 min. Modification of phosphonate on silica increased the adsorption capability, up to 8 times higher than that of unmodified silica, depending on metal ion type and pH solution. The capacity order of the metals adsorption was Cu(II>Co(II>Ni(II>Zn(II. Based on the adsorption characteristic, the adsorbent is promising to be applied as a material for solid phase extraction of transition metal ions.

  19. Ni(II) complexes of dithiophosphonic acids

    Indian Academy of Sciences (India)

    bacterial properties. ∗. For correspondence. Three novel dithiophosphinates with the formula HS2P. (p-C6H4OMe)(OCH2CH(CH3)2) (I), [S2P(C6H11NH)(p-. C6H4OMe)H3N. +. C6H11] (II) and [S2P(phCH2CH2NH). (p-C6H4OMe)H3N. +.

  20. Synthesis and spectroscopic studies of biologically active tetraazamacrocyclic complexes of Mn(II, Co(II, Ni(II, Pd(II and Pt(II

    Directory of Open Access Journals (Sweden)

    Monika Tyagi

    2014-01-01

    Full Text Available Complexes of Mn(II, Co(II, Ni(II, Pd(II and Pt(II were synthesized with the macrocyclic ligand, i.e., 2,3,9,10-tetraketo-1,4,8,11-tetraazacycoletradecane. The ligand was prepared by the [2 + 2] condensation of diethyloxalate and 1,3-diamino propane and characterized by elemental analysis, mass, IR and 1H NMR spectral studies. All the complexes were characterized by elemental analysis, molar conductance, magnetic susceptibility measurements, IR, electronic and electron paramagnetic resonance spectral studies. The molar conductance measurements of Mn(II, Co(II and Ni(II complexes in DMF correspond to non electrolyte nature, whereas Pd(II and Pt(II complexes are 1:2 electrolyte. On the basis of spectral studies an octahedral geometry has been assigned for Mn(II, Co(II and Ni(II complexes, whereas square planar geometry assigned for Pd(II and Pt(II. In vitro the ligand and its metal complexes were evaluated against plant pathogenic fungi (Fusarium odum, Aspergillus niger and Rhizoctonia bataticola and some compounds found to be more active as commercially available fungicide like Chlorothalonil.

  1. Dynamic Adsorption Studies for the Removal of Cd (II) and Ni (II ...

    African Journals Online (AJOL)

    MBI

    2016-12-17

    Dec 17, 2016 ... ABSTRACT. A dynamic adsorption study was carried out using mahogany leaves (ML) powder as an adsorbent for the removal of Cd (II) and Ni (II) from their aqueous solutions. The effects of contact time, adsorbent dose (5, 10 and 15 g), initial concentration (10, 15 and 20 mg/L), particle size (212, 150 and ...

  2. Synthesis, Characterization and Thermal Studies of Co(II), Ni(II), Cu ...

    African Journals Online (AJOL)

    NICO

    2010-06-15

    Jun 15, 2010 ... Ni(II) and Zn(II). TG curves indicated that the complexes decompose in three to four steps. The presence of coordinated water in metal complexes was confirmed by thermal and IR data of the complexes. KEY WORDS. Synthesis, Schiff bases, 1,2,4-triazine, thermal study. 1. Introduction. Triazine chemistry ...

  3. Magnetic, thermal and spectroscopic properties of 5-chloro-2-methoxybenzoates of Mn(II, Co(II, Ni(II, Cu(II and Zn(II

    Directory of Open Access Journals (Sweden)

    BEATA BOCIAN

    2002-09-01

    Full Text Available The 5-chloro-2-methoxybenzoates of Mn(II, Co(II, Ni(II, Cu(II and Zn(II were synthesized as solids and their magnetic, spectral and thermal properties studied. The complexes possess colours typical of the M(II ions. The thermal stabilities were examined in air and nitrogen atmospheres and the products of decompositions were also identified. The magnetic susceptibilities of the complexes were measured over the temperature range 4.4–300 K and the magnetic moments were calculated. The results show that the 5-chloro-2-methoxybenzoates of Mn(II, Co(II and Ni(II are octahedral, high-spin complexes.

  4. Breakdown of antiferromagnet order in polycrystalline NiFe/NiO bilayers probed with acoustic emission

    Science.gov (United States)

    Lebyodkin, M. A.; Lebedkina, T. A.; Shashkov, I. V.; Gornakov, V. S.

    2017-07-01

    Magnetization reversal of polycrystalline NiFe/NiO bilayers was investigated using magneto-optical indicator film imaging and acoustic emission techniques. Sporadic acoustic signals were detected in a constant magnetic field after the magnetization reversal. It is suggested that they are related to elastic waves excited by sharp shocks in the NiO layer with strong magnetostriction. Their probability depends on the history and number of repetitions of the field cycling, thus testifying the thermal-activation nature of the long-time relaxation of an antiferromagnetic order. These results provide evidence of spontaneous thermally activated switching of the antiferromagnetic order in NiO grains during magnetization reversal in ferromagnet/antiferromagnet (FM/AFM) heterostructures. The respective deformation modes are discussed in terms of the thermal fluctuation aftereffect in the Fulcomer and Charap model which predicts that irreversible breakdown of the original spin orientation can take place in some antiferromagnetic grains with disordered anisotropy axes during magnetization reversal of exchange-coupled FM/AFM structures. The spin reorientation in the saturated state may induce abrupt distortion of isolated metastable grains because of the NiO magnetostriction, leading to excitation of shock waves and formation of plate (or Lamb) waves.

  5. Biologically active new Fe(II, Co(II, Ni(II, Cu(II, Zn(II and Cd(II complexes of N-(2-thienylmethylenemethanamine

    Directory of Open Access Journals (Sweden)

    C. SPÎNU

    2008-04-01

    Full Text Available Iron(II, cobalt(II, nickel (II, copper (II, zinc(II and cadmium(II complexes of the type ML2Cl2, where M is a metal and L is the Schiff base N-(2-thienylmethylenemethanamine (TNAM formed by the condensation of 2-thiophenecarboxaldehyde and methylamine, were prepared and characterized by elemental analysis as well as magnetic and spectroscopic measurements. The elemental analyses suggest the stoichiometry to be 1:2 (metal:ligand. Magnetic susceptibility data coupled with electronic, ESR and Mössbauer spectra suggest a distorted octahedral structure for the Fe(II, Co(II and Ni(II complexes, a square-planar geometry for the Cu(II compound and a tetrahedral geometry for the Zn(II and Cd(II complexes. The infrared and NMR spectra of the complexes agree with co-ordination to the central metal atom through nitrogen and sulphur atoms. Conductance measurements suggest the non-electrolytic nature of the complexes, except for the Cu(II, Zn(II and Cd(II complexes, which are 1:2 electrolytes. The Schiff base and its metal chelates were screened for their biological activity against Escherichia coli, Staphylococcus aureus and Pseudomonas aeruginosa and the metal chelates were found to possess better antibacterial activity than that of the uncomplexed Schiff base.

  6. Potentiometric and spectrophotometric studies of Mn{sup II} and Ni{sup II} cimetidine complexes

    Energy Technology Data Exchange (ETDEWEB)

    Kanumfre, Francieli; Lima, Eliane M. de; Scheidt, Gabriele; Carneiro, Paulo I.B.; Rosso, Neiva D., E-mail: ndrosso@uepg.b [Universidade Estadual de Ponta Grossa, PR (Brazil). Dept. de Quimica

    2010-07-01

    Cimetidine is an important hydrogen histamine receptor which has the ability to chelate metal ions in blood plasma and in different tissues. This study aimed to determine the stability constants for the cimetidine ligand with Mn{sup II} and Ni{sup II} metallic ions, synthesizing complexes and characterizing them by infrared spectroscopy, IR, and hydrogen nuclear magnetic resonance, {sup 1}H NMR. Cimetidine protonation constant regarding to the imidazole group was log K 7.05 and the stability constants for Mn{sup II} and Ni{sup II} complexes, ML{sub 2} species were log K 3.75 and 2.97, respectively, in 0.100 mol L{sup -1} KCl. The interpretation of IR and {sup H}1 NMR spectra for complexes Mn{sup II}-cim{sub 2} and Ni{sup II}-cim{sub 2} indicated that their formation occurs through the sulfur atoms in the thiol group, nitrogen atoms of imidazole ring, and nitrogen atoms of secondary amine. The nitrile group seems to be involved in the complexation of the Ni{sup II}-cim{sub 2} complex. (author)

  7. Removal of Ni(II), Zn(II) and Pb(II) ions from single metal aqueous solution using rice husk-based activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Taha, Mohd F., E-mail: faisalt@petronas.com.my; Shaharun, Maizatul S. [Fundamental and Applied Sciences Department, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 31750, Perak Darul Ridzuan (Malaysia); Shuib, Anis Suhaila, E-mail: anisuha@petronas.com.my; Borhan, Azry [Chemical Engineering Department, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 31750, Perak Darul Ridzuan (Malaysia)

    2014-10-24

    An attempt was made to investigate the potential of rice husk-based activated carbon as an alternative low-cost adsorbent for the removal of Ni(II), Zn(II) and Pb(II) ions from single aqueous solution. Rice husk-based activated carbon was prepared via treatment of rice husk with NaOH followed by the carbonization process at 400°C for 2 hours. Three samples, i.e. raw rice husk, rice husk treated with NaOH and rice husk-based activated carbon, were analyzed for their morphological characteristics using field-emission scanning electron microscope/energy dispersive X-ray (FESEM/EDX). These samples were also analyzed for their carbon, hydrogen, nitrogen, oxygen and silica contents using CHN elemental analyzer and FESEM/EDX. The porous properties of rice husk-based activated carbon were determined by Brunauer-Emmett-Teller (BET) surface area analyzer, and its surface area and pore volume were 255 m{sup 2}/g and 0.17 cm{sup 2}/g, respectively. The adsorption studies for the removal of Ni(II), Zn(II) and Pb(II) ions from single metal aqueous solution were carried out at a fixed initial concentration of metal ion (150 ppm) with variation amount of adsorbent (rice husk-based activated carbon) as a function of varied contact time at room temperature. The concentration of each metal ion was analyzed using atomic absorption spectrophotometer (AAS). The results obtained from adsorption studies indicate the potential of rice husk as an economically promising precursor for the preparation of activated carbon for removal of Ni(II), Zn(II) and Pb(II) ions from single aqueous solution. Isotherm and kinetic model analyses suggested that the experimental data of adsorption studies fitted well with Langmuir, Freundlich and second-order kinetic models.

  8. Adsorption of Ni(II and Cd(II from Aqueous Solutions Using Modified Rice Husk

    Directory of Open Access Journals (Sweden)

    Soheil Sobhanardakani

    2015-03-01

    Full Text Available Background and purpose: Recently, release of pollutants such as heavy metal ions to the environment becomes one of the most important problems for soil and water. The present study was conducted to introduce modified rice husk (RH as a new low-cost adsorbent. Materials and Methods: In this study, tartaric acid modified RH (TARH, was used as an adsorbent for removal of Ni(II and Cd(II from water samples. This study was conducted in laboratory scale. Employing batch method, solution pH, adsorbent dose, contact time, and initial metals concentration were optimized. Results: The optimum pH for removing of both the investigated metal ions from water solutions was found to be 4.0. The process of Ni(II and Cd(II adsorption on TARH reached equilibrium within 45 min. The isotherm evaluations revealed that the Langmuir model attained better fits of the experimental equilibrium data than the Freundlich model. In addition, adsorption kinetics data were well-fitted by the pseudo-second-order rate model with high regression coefficients. Conclusion: It was found that TARH is a highly efficient adsorbent for Ni and Cd from aqueous solution, and the maximum predicted adsorption capacities for Ni(II and Cd(II were obtained as 55.5 and 45.5 mg/g, respectively.

  9. Thermoanalytical studies of cimetidine and complexes with Mn(II) Co(II) and Ni(II)

    OpenAIRE

    Ana Carolina Mendes Hacke; Fernanda Moreira; Egon Schnitzler; Neiva Deliberali Rosso

    2014-01-01

    Cimetidine is an important hydrogen histamine receptor and can coordinate metal ions in blood plasma. The stability of cimetidine and its complexes with Mn(II), Co(II) and Ni(II) was evaluated by studies of thermogravimetry (TG) and differential thermal analysis (DTA). Cimetidine was thermally stable up to near 190 °C and above this temperature the thermal decomposition occurred in two stages. Complexes of [Mn(HCm)2]Cl2, [Co(Cm)2]Cl2 and [Ni(Cm)2]Cl2 showed a similar behavior. The pyrolytic d...

  10. COMPARATIVE CHARACTERISTICS OF Co(II, Ni (II, Cu(II COORDINATION COMPOUNDS WITH SOME HYDRAZONES OF PYRUVIC ACID

    Directory of Open Access Journals (Sweden)

    A. V. Pulya

    2016-11-01

    Full Text Available Сonducted comparative analysis of the coordination compounds of Co2+, Ni2+, Cu2+ with condensation products of 2-(7-bromo-2-oxo-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepin-1-yl acetohydrazide – Hydazepam (Hydr, nicotinoyl- and isonicotinoyl hydrazones (H2N, H2I with pyruvic acid (HPv: [Co(HydrHPvCl2]·2H2O (I, [Ni(HydrPv2] (II, [Cu(HydrHPv (H2OCl2] (III, [CoCl(HNPv(H2O2] (IV, [CoCl(HIPv(H2O2] (V, [NiCl(HNPv(H2O2] (VI, [NiCl(HIPv(H2O2] (VII, [CuCl(HNPv]·H2O (VIII, [CuCl(HIPv]·H2O (IX. Complexes characterized by elemental analysis, IR spectroscopy, electrical conductivity, and magnetic susceptibility. Thermal stability of the complexes has been characterized. Structure of the coordination node of the complexes has been determined by EXAFS-spectroscopy. Regardless of composition, structure by heterocyclic nitrogen-containing moiety of the molecules HydrHPv, H2NРv, H2IРv formation of I-IX complexes is due to binding of complexing with a hydrazide functional group ketone form of the ligands. Ni2+ complexes II, VI, VII are different by composition (Ni2+:HydrHPv в II = 1:2, Ni2+:H2NРv(H2IРv в VI, VII = 1:1. Co2+, Cu2+ complexes with the same composition (M2+:ligand = 1:1. H2NPv, H2IPv in all complexes IV-IX – tridentate, occurs deprotonation and bonding carboxylate group НPv. HydrHPv coordinated to the Co2+, Cu2+ bidentate (I, III, without participation of the carboxylic group, and to the Ni2+ – tridentate (II.

  11. SPECIATION OF L-ASPARTIC ACID COMPLEXES OF Co(II), Ni(II ...

    African Journals Online (AJOL)

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    Cobalt is essential for the production of the red blood cells and cobalamin acts as the substrate for the final enzymatic reaction that yields the active coenzyme derivatives of cyanocobalamin and aquacobalamin. Nickel is found in enzymes, such as urease, which is a dinuclear Ni(II)-containing metalloenzyme [8-10].

  12. One-dimensional Co(II)/Ni(II) complexes of 2-hydroxyisophthalate: Structures and magnetic properties

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Kai [Coordination Chemistry Institute, State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing National Laboratory of Microstructures, Nanjing University, Nanjing 210093 (China); State Key Laboratory Cultivation Base for the Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmacy, Guangxi Normal University, Guilin 541004 (China); Zou, Hua-Hong; Chen, Zi-Lu; Zhang, Zhong [State Key Laboratory Cultivation Base for the Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmacy, Guangxi Normal University, Guilin 541004 (China); Sun, Wei-Yin [Coordination Chemistry Institute, State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing National Laboratory of Microstructures, Nanjing University, Nanjing 210093 (China); Liang, Fu-Pei, E-mail: fliangoffice@yahoo.com [State Key Laboratory Cultivation Base for the Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmacy, Guangxi Normal University, Guilin 541004 (China); College of Chemistry and Bioengineering, Guilin University of Technology, Guilin 541004 (China)

    2015-03-15

    The solvothermal reactions of 2-hydroxyisophthalic acid (H{sub 3}ipO) with M(NO{sub 3}){sub 2}∙6H{sub 2}O (M=Co, Ni) afforded two complexes [Co{sub 2}(HipO){sub 2}(Py){sub 2}(H{sub 2}O){sub 2}] (1) and [Ni(HipO)(Py)H{sub 2}O] (2) (Py=pyridine). They exhibit similar zig-zag chain structures with the adjacent two metal centers connected by a anti-syn bridging carboxylate group from the HipO{sup 2−} ligand. The magnetic measurements reveal the dominant antiferromagnetic interactions and spin-canting in 1 while ferromagnetic interactions in 2. Both of them exhibit magnetocaloric effect (MCE) with the resulting entropy changes (−ΔS{sub m}) of 12.51 J kg{sup −1} K{sup −1} when ΔH=50 kOe at 3 K for 1 and 11.01 J kg{sup −1} K{sup −1} when ΔH=50 kOe at 3 K for 2, representing the rare examples of one-dimensional complexes with MCE. - Graphical abstract: Synopsis: Two Co(II)/Ni(II) complexes with zig-zag chain structures have been reported. 1-Co shows cant-antiferromagnetism while 2-Ni shows ferromagnetism. Magnetocaloric effect is also found in both of them. - Highlights: • Two one-dimensional Co(II)/Ni(II) complexes were solvothermally synthesized. • The Co-complex exhibits canted antiferromagnetism. • The Ni-complex exhibits ferromagnetism. • Both of the complexes display magnetocaloric effect.

  13. Heterometallic Pd(II)-Ni(II) complexes with meso-substituted dibenzotetraaza[14]annulene: double C-H bond activation and formation of a rectangular tetradibenzotetraaza[14]annulene.

    Science.gov (United States)

    Khaledi, Hamid; Olmstead, Marilyn M; Fukuda, Takamitsu; Ali, Hapipah Mohd

    2014-11-03

    Three isomeric 2[Pd(II)-Ni(II)] metal complexes, derived from indoleninyl meso-substituted dibenzotetraaza[14]annulene, were synthesized. The resulting dimers feature Ni···Ni or, alternatively, Ni···π interactions in staggered or slipped cofacial structures. A remarkable insertion of palladium into two different C-H bonds yielded a 4[Pd(II)-Ni(II)] rectangular complex with dimensions of 8.73 × 10.38 Å.

  14. Physicochemical properties of 3,4,5-trimethoxybenzoates of Mn(II, Co(II, Ni(II and Zn(II

    Directory of Open Access Journals (Sweden)

    W. FERENC

    2005-09-01

    Full Text Available The complexes of Mn(II, Co(II, Ni(II, Cu(II and Zn(II with 3,4,5-trimethoxybenzoic acid anion of the formula: M(C10H11O52·nH2O, where n = 6 for Ni(II, n = 1 for Mn(II, Co(II, Cu(II, and n = 0 for Zn, have been synthesized and characterized by elemental analysis, IR spectroscopy, X–ray diffraction measurements, thermogravimetry and magnetic studies. They are crystalline compounds characterized by various symmetry. They decompose in various ways when heated in air to 1273 K. At first, they dehydrate in one step and form anhydrous salts. The final products of decomposition are oxides of the respective metals (Mn2O3, Co3O4, NiO, CuO, ZnO. The solubilities of the analysed complexes in water at 293 K are in the orders of 10-2 – 10-4 mol dm-3. The magnetic susceptibilities of the Mn(II, Co(II, Ni(II and Cu(II complexes were measured over the range of 76–303 K and the magnetic moments were calculated. The results show that the 3,4,5-trimethoxybenzoates of Mn(II, Co(II and Ni(II are high-spin complexes but that of Cu(II forms a dimer [Cu2(C10H11O54(H2O2]. The carboxylate groups bind as monodentate or bidentate chelating or bridging ligands.

  15. Synthesis, characterization and anti-microbial evaluation of Cu(II), Ni(II), Pt(II) and Pd(II) sulfonylhydrazone complexes; 2D-QSAR analysis of Ni(II) complexes of sulfonylhydrazone derivatives

    Science.gov (United States)

    Özbek, Neslihan; Alyar, Saliha; Alyar, Hamit; Şahin, Ertan; Karacan, Nurcan

    2013-05-01

    Copper(II), nickel(II), platinum(II) and palladium(II) complexes with 2-hydroxy-1-naphthaldehyde-N-methylpropanesulfonylhydrazone (nafpsmh) derived from propanesulfonic acid-1-methylhydrazide (psmh) were synthesized, their structure were identified, and antimicrobial activity of the compounds was screened against three Gram-positive and three Gram-negative bacteria. The results of antimicrobial studies indicate that Pt(II) and Pd(II) complexes showed the most activity against all bacteria. The crystal structure of 2-hydroxy-1-naphthaldehyde-N-methylpropanesulfonylhydrazone (nafpsmh) was also investigated by X-ray analysis. A series of Ni(II) sulfonyl hydrazone complexes (1-33) was synthesized and tested in vitro against Escherichia coli and Staphylococcus aureus. Their antimicrobial activities were used in the QSAR analysis. Four-parameter QSAR models revealed that nucleophilic reaction index for Ni and O atoms, and HOMO-LUMO energy gap play key roles in the antimicrobial activity.

  16. FINE-STRUCTURE Fe II* EMISSION AND RESONANT Mg II EMISSION IN z ∼ 1 STAR-FORMING GALAXIES

    International Nuclear Information System (INIS)

    Kornei, Katherine A.; Shapley, Alice E.; Martin, Crystal L.; Coil, Alison L.; Lotz, Jennifer M.; Weiner, Benjamin J.

    2013-01-01

    We present a study of the prevalence, strength, and kinematics of ultraviolet Fe II and Mg II emission lines in 212 star-forming galaxies at z ∼ 1 selected from the DEEP2 survey. We find Fe II* emission in composite spectra assembled on the basis of different galaxy properties, indicating that Fe II* emission is common at z ∼ 1. In these composites, Fe II* emission is observed at roughly the systemic velocity. At z ∼ 1, we find that the strength of Fe II* emission is most strongly modulated by dust attenuation, and is additionally correlated with redshift, star formation rate, and [O II] equivalent width, such that systems at higher redshifts with lower dust levels, lower star formation rates, and larger [O II] equivalent widths show stronger Fe II* emission. We detect Mg II emission in at least 15% of the individual spectra and we find that objects showing stronger Mg II emission have higher specific star formation rates, smaller [O II] linewidths, larger [O II] equivalent widths, lower dust attenuations, and lower stellar masses than the sample as a whole. Mg II emission strength exhibits the strongest correlation with specific star formation rate, although we find evidence that dust attenuation and stellar mass also play roles in the regulation of Mg II emission. Future integral field unit observations of the spatial extent of Fe II* and Mg II emission in galaxies with high specific star formation rates, low dust attenuations, and low stellar masses will be important for probing the morphology of circumgalactic gas

  17. Average [O II]nebular emission associated with Mg II absorbers: Dependence on Fe II absorption

    Science.gov (United States)

    Joshi, Ravi; Srianand, Raghunathan; Petitjean, Patrick; Noterdaeme, Pasquier

    2018-01-01

    We investigate the effect of Fe II equivalent width (W2600) and fibre size on the average luminosity of [O II]λλ3727,3729 nebular emission associated with Mg II absorbers (at 0.55 ≤ z ≤ 1.3) in the composite spectra of quasars obtained with 3 and 2 arcsec fibres in the Sloan Digital Sky Survey. We confirm the presence of strong correlations between [O II] luminosity (L_{[O II]}) and equivalent width (W2796) and redshift of Mg II absorbers. However, we show L_{[O II]} and average luminosity surface density suffers from fibre size effects. More importantly, for a given fibre size the average L_{[O II]} strongly depends on the equivalent width of Fe II absorption lines and found to be higher for Mg II absorbers with R ≡W2600/W2796 ≥0.5. In fact, we show the observed strong correlations of L_{[O II]} with W2796 and z of Mg II absorbers are mainly driven by such systems. Direct [O II] detections also confirm the link between L_{[O II]} and R. Therefore, one has to pay attention to the fibre losses and dependence of redshift evolution of Mg II absorbers on W2600 before using them as a luminosity unbiased probe of global star formation rate density. We show that the [O II] nebular emission detected in the stacked spectrum is not dominated by few direct detections (i.e., detections ≥3σ significant level). On an average the systems with R ≥0.5 and W2796 ≥2Å are more reddened, showing colour excess E(B - V) ˜ 0.02, with respect to the systems with R <0.5 and most likely traces the high H I column density systems.

  18. A mixed Ni(II) ionic complex containing V-shaped water trimer ...

    Indian Academy of Sciences (India)

    A mixed Ni(II) ionic complex containing V-shaped water trimer: Synthesis, spectral, structural and thermal properties of. {[Ni(2,2. ′. -bpy)3][Ni(2-cpida)(2,2. ′. -bpy)]} (ClO4).3H2O. NALLASAMY PALANISAMIa, KABALI SENTHILKUMARb, MOHAN GOPALAKRISHNANb and IL-SHIK MOONa,∗. aDepartment of Chemical ...

  19. Ferromagnetic interactions in new double end-on-azide-bridged dinuclear Ni(II) complex: Synthesis, crystal structures, magnetic and photoluminescence properties

    Science.gov (United States)

    Donmez, Adem; Oylumluoglu, Gorkem; Coban, M. Burak; Kocak, Cagdas; Aygun, Muhittin; Kara, Hulya

    2017-12-01

    A new double end-on azide-bridged dinuclear nickel(II) Schiff base complex, [Ni2(μ1,1-N3)2(HL)2(MeOH)2], [HL = 2-[(2-hydroxypropylimino)methyl)-3,5-chlorophenol] has been synthesized and characterized by elemental analysis, UV and IR spectroscopy, single crystal X-ray diffraction, magnetic and photoluminescence study. The asymmetric unit contains half of the dinuclear unit. The Ni(HL) units in each dinuclear molecule are connected to each other by two bridging end-on azide ligands. In the crystalline architecture of the Ni(II) complex, intermolecular Osbnd H⋯N hydrogen bonds link the molecules which form one-dimensional structure. Additionally, low temperature magnetic measurements indicate a dominant intradimer ferromagnetic interactions in double end-on azide-bridged dinuclear Ni(II) complex. Room temperature solid state photoluminescence measurements of Ni(II) complex show strong green emission band at λmax = 508 nm while its free ligand H2L shows broad yellow emission band at λmax = 594 nm. The luminescent performances making Ni(II) complex may be good candidates for potential luminescence materials.

  20. Thermoanalytical studies of cimetidine and complexes with Mn(II Co(II and Ni(II

    Directory of Open Access Journals (Sweden)

    Ana Carolina Mendes Hacke

    2014-02-01

    Full Text Available Cimetidine is an important hydrogen histamine receptor and can coordinate metal ions in blood plasma. The stability of cimetidine and its complexes with Mn(II, Co(II and Ni(II was evaluated by studies of thermogravimetry (TG and differential thermal analysis (DTA. Cimetidine was thermally stable up to near 190 °C and above this temperature the thermal decomposition occurred in two stages. Complexes of [Mn(HCm2]Cl2, [Co(Cm2]Cl2 and [Ni(Cm2]Cl2 showed a similar behavior. The pyrolytic decomposition occurred in two stages at temperatures above 250 oC. A residue for each complex was detected at the end of the decomposition process. This probably corresponds to the respective metal oxide.

  1. Potentiometric study of atenolol as hypertension drug with Co(II, Ni(II, Cu(II and Zn(II transition metal ions in aqueous solution

    Directory of Open Access Journals (Sweden)

    Abdulbaset A. Zaid

    2015-01-01

    Full Text Available Binary and ternary complexes of Co(II, Ni(II, Cu(II and Zn(II with atenolol as hypertension drug and glycine have been determined pH metrically at room temperature and 0.01 M ionic strength (NaClO4 in aqueous solution. The formation of various possible species has been evaluated by computer program and discussed in terms of various relative stability parameters.

  2. Unsaturated b-ketoesters and their Ni(II, Cu(II and Zn(II complexes

    Directory of Open Access Journals (Sweden)

    MUHAMMED BASHEER UMMATHUR

    2009-03-01

    Full Text Available A new series of b-ketoesters in which the keto group is attached to the olefinic linkage were synthesized by the reaction of methyl acetoacetate and aromatic aldehydes under specified conditions. The existence of these compounds predominantly in the intramolecularly hydrogen bonded enol form was well demonstrated from their IR, 1H-NMR and mass spectral data. Details on the formation of their [ML2] complexes with Ni(II, Cu(II and Zn(II and the nature of the bonding are discussed on the basis of analytical and spectral data.

  3. Optimal synthesis of a Ni(II)-dimethylglyoxime ion-imprinted polymer ...

    African Journals Online (AJOL)

    A Ni(II)-dimethylglyoxime ion-imprinted polymer {Ni(II)-DMG IIP} was optimised by the uniform design experimental ... The bonds formed between the template and the functional monomers in ion- imprinted polymerisation reactions are weaker, non-covalent. (Arshady and Mosbach, 1981; ..... where the polymer did not form.

  4. Adsorption study on orange peel: Removal of Ni(II) ions from ...

    African Journals Online (AJOL)

    orange peel was investigated to evaluate the effects of pH, initial nickel ion concentration and adsorbent dose on the removal of Ni(II) systematically. The optimal pH value for Ni(II) adsorption onto the orange peel was found to be 5.0. Greater ...

  5. Effect of boron on enhancing infrared emissivity of Ni-Cr system coating

    Science.gov (United States)

    Li, Yongjia; Ouyang, Taoyuan; Wang, Xiaohuan; Li, Shuhao; Mao, Jiawei; Cheng, Xudong

    2018-03-01

    High infrared emissivity coating possesses great value in practical application, whether in the military or civilian areas. In this study, B-NiCr precursor powder containing NiO, Cr2O3 and ZrB2 was calcined at 1300 °C and then used to prepare a high infrared emissivity B-NiCr coating via atmospheric plasma spraying. A large number of test methods were employed to analyze the powder and coating, including TG-DSC, XRD, FE-SEM, infrared spectrometer and so on. The result of infrared emissivity measurement indicates that the coating possesses maximum infrared emissivity of 0.908 at 1000 °C while the infrared emissivity is 0.901 after thermal shock test. Comparing with NiCr coating, Ni2CrO2(BO3) formed during calcination may be the main factor to improve the infrared emissivity of B-NiCr coating. The B-NiCr coating possesses good thermal shock resistance and can withstand 50 times thermal shock at least without falling off, from 800 °C to room temperature.

  6. Biosorption of Cr(VI), Ni(II) and Fe(II) by maize ( zea mays ) cob ...

    African Journals Online (AJOL)

    The experimental results for the biosorption of Cr(VI), Ni(II) and Fe(II) onto maize cob were reported. The adsorbents efficiency on the bioremediation of these metals was estimated from the change in the percent adsorbate removal with (i) adsorbent dosage (ii) adsorbate initial concentration, (iii) variation in pH of the ...

  7. Cr(III,Mn(II,Fe(III,Co(II,Ni(II,Cu(II and Zn(II Complexes with Diisobutyldithiocarbamato Ligand

    Directory of Open Access Journals (Sweden)

    Mohammad Tarique

    2011-01-01

    Full Text Available The synthesis of sulphur and nitrogen containing dithiocarbamato ligand derived from diisobutylamine as well as its coordination compounds with 3d series transition metals is presented. These synthesized compounds were characterized on the basis of elemental analysis, conductometric measurements and IR spectral studies. The analytical data showed the stoichiometry 1:2 and 1:3 for the compounds of the types ML2 {M=Mn(II, Co(II, Ni(II, Cu(II and Zn(II} and M'L3{M'=Cr(III and Fe(III} respectively. The conductometric measurements proved the non-electrolytic behaviour of all the compounds. The bidentate nature of dithiocarbamato moiety was confirmed on the basis of IR spectral data.

  8. Antiviral Activity of Substituted Chalcones and their Respective Cu(ii, Ni(ii and Zn(ii Complexes

    Directory of Open Access Journals (Sweden)

    K. G. Mallikarjun

    2005-01-01

    Full Text Available Complexes of Cu(II, Ni(II and Zn(II with of 3-(phenyl-1-(2’-hydroxynaphthyl – 2 – propen – 1 – one (PHPO , 3 - (4-chlorophenyl - 1- (2’-hydroxynaphthyl–2–propen – 1 – one (CPHPO, 3 - (4 -methoxyphenyl -1-(2’-hydroxynapthyl-2-propen-1-one(MPHPO,3 - (3,4-dimethoxyphenyl –1-(2’-hydroxynaphthyl – 2 - propen– 1 – one (DMPHPO have been prepared and the purity of the samples were checked by elemental analysis. The ligands and their Cu(II, Ni(II and Zn(II complexes were tested on the infectivity of tobacco ring spot virus(TRSV using cowpea (Vigna Sinensis as a local lesions assay host. All the compounds were tested at different concentrations (250 ppm to 1500 ppmon the infectivity of the virus by applying them either with virus inoculum or 24 h before of after virus inoculation to the test plants. The compounds were found to have varied effects on virus infectivity depending on compounds concentration and method of application. The statistical significance of the data was determined by using analysis of variance.

  9. Structural characterization and antioxidant properties of Cu(II) and Ni(II) complexes derived from dicyandiamide

    Science.gov (United States)

    Kertmen, Seda Nur; Gonul, Ilyas; Kose, Muhammet

    2018-01-01

    New Cu(II) and Ni(II) complexes derived from dicyandiamide were synthesized and characterised by spectroscopic and analytical methods. Molecular structures of the complexes were determined by single crystal X-ray diffraction studies. In the complexes, the Cu(II) or Ni(II) ions are four-coordinate with a slight distorted square planar geometry. The ligands (L-nPen and L-iPen) derived from dicyandiamide formed via nucleophilic addition of alcohol solvent molecule in the presence Cu(II) or Ni(II) ions. Complexes were stabilised by intricate array of hydrogen bonding interactions. Antioxidant activity of the complexes was evaluated by DPPH radical scavenging and CUPRAC methods. The complexes exhibit antioxidant activity, however, their activities were much lower than standard antioxidants (Vitamin C and trolox).

  10. Chelating Schiff base assisted azide-bridged Mn(II), Ni(II) and Cu(II) magnetic coordination polymers.

    Science.gov (United States)

    Bai, Shi-Qiang; Fang, Chen-Jie; He, Zheng; Gao, En-Qing; Yan, Chun-Hua; Hor, T S Andy

    2012-11-21

    Four new Mn(II), Ni(II) and Cu(II) coordination polymers [Mn2(L1)(μ(1,1)-N3)2(μ(1,3)-N3)2]n (1), [Ni(L2)2(μ(1,3)-N3)]n(ClO4)n (2), [Cu(L3)(μ(1,1)-N3)(N3)]n (3) and [Cu(L4)(μ(1,1)-N3)2]n (4) (L1 = N,N′-bis(2-pyridylmethylene)ethane-1,2-diamine, L2 = N-(2-pyridylmethylene)methylamine, L3 = N-(2-pyridylmethylene)-3-pyridylamine, L4 = N-(2-pyridylmethylene)-tbutylamine) have been synthesized and characterized by single-crystal X-ray analysis and magnetic measurements. Complex 1 indicates a stoichiometry-dependent structural change (based on Mn:L1:N3 = 2:1:4 molar ratio) and consists of two-dimensional (2-D) (4,4) net layers, in which Mn(II) centers are co-bridged by single end-to-end (EE), double end-on (EO) azide and chelate-bridging L1 ligands. Complex 2 shows a single EE azide-bridged one-dimensional (1-D) Ni(II) chain. Complexes 3 and 4 indicate single EO and double EO azide-bridged 1-D Cu(II) chains, respectively. Complex 1 exhibits weak ferromagnetism due to its intra-layer spin-canting with T(c) = 20 K. Complex 2 shows an unusual intra-chain ferromagnetic coupling and spin-canting behaviour. Both complexes 3 and 4 exhibit intra-chain antiferromagnetic interactions. Magneto-structural parameters for these related complexes were also discussed.

  11. Template Synthesis, Characterization and Biological Activity of Cu(II, Ni(II, Co(II, Zn(IIComplexes with Isonicotinoylhydrazone--2-aldehydefluorene Ligand

    Directory of Open Access Journals (Sweden)

    2010-01-01

    Full Text Available This is about synthesizing new complex combinations of Cu(II, Ni(II,Co(II, Zn(II with aroylhydrazone ligand isonicotinoylhydrazone-2-aldehydefluorene (INHAF made by condensation of isonicotinoylhydrazine with 2-aldehydefluorene. The complexes have been characterized by analytical data, IR, UV-Vis, NMR spectra, magnetic susceptibility values, thermal analysis and for the Cu(II complex the ESR spectrum has been registered. For all complexes the biological activity against the Staphylo-coccus aureus, Escherichia coli, Klebssiella pneumoniae bacteria has been investigated. The experimental data sustain stoichiometry of 1:2 (metal/ligand for the Cu(II, Ni(II, Zn(II complexes and of 1:1 for the complex with Co(II. The electronic spectra and the magnetic moments suggest octahedral stereochemistry at the complexes with Cu(II, Ni(II and the tetrahedral geometry for the Co(II complex. The INHAF ligand is coordinated bidentate by the O=C amide oxygen and the azomethine nitrogen in the complexes of Cu(II, Ni(II, Co(II and monodentate by the azomethine nitrogen in the complex of Zn(II.

  12. Synthesis, characterization and cytotoxicity of mixed ligand Mn(II, Co(II and Ni(II complexes

    Directory of Open Access Journals (Sweden)

    Osman Souad A.

    2014-01-01

    Full Text Available Complexes of the type [ML'L(OH(H2O] {where M= Ni(II, Co(II or Mn(II, L'= isatin and HL= 3-(2-phenylhydrazonoacetylacetone, 3-(2-(4-chlorophenylhydrazonoacetylacetone or 3-(2-(4-bromophenylhydrazono-acetylacetone} have been synthesized by equimolar reaction of a metal(II chloride with isatin and 3-(2-(arylhydrazonoacetylacetone. The resulting complexes have been characterized by elemental analyses, molar conductivity, spectral data (IR, 1H NMR, mass and magnetic moments. Furthermore, the ligands and their metal complexes have been screened for their cytotoxicity against different human cancer cell lines by using SRB assay. The results showed that most of the mixed ligand metal complexes have high cytotoxicity in comparison with the reference drugs used.

  13. FORMATION OF BINARY COMPLEXES OF Co(II), Ni(II) AND Cu(II ...

    African Journals Online (AJOL)

    Preferred Customer

    INTRODUCTION. Cobalt(II), nickel(II) and copper(II) are associated with several enzymes [1, 2] and any variation ... amounts (10 mg/day), at higher levels of exposure it shows mutagenic and carcinogenic effects. [13]. Minot and ... Nickel plays numerous roles in the biology of microorganisms and plants [15, 16]. Urease, an.

  14. Selective Extraction of Co(II in the Presence of Mn(II, Ni(II and Cu(II Using Salting-out Phase Separation Method

    Directory of Open Access Journals (Sweden)

    A M Shafiqul Alam

    2008-06-01

    Full Text Available Extraction of Co(II in the presence of Mn(II, Ni(II and Cu(II has been studied using the mixture of 2-propanol with water upon the addition of CaCl2 in the concentration range of 3.0 – 5.0 mol dm-3 (M. Co(II was extracted selectively to the extent of 80% into the 2-propanol phase at 5.0 M CaCl2. The percent of extraction of other transition metal ions, for example Mn(II, Ni(II and Cu(II was much lower than that of Co(II, but they were stripped in the aqueous phase upon addition of CaCl2. Therefore, selective extraction of Co(II from these metal ions was attained by using the mixture of water and 2-propanol. Co(II was extracted as CoCl42- from the aqueous phase into the 2-propanol phase through the formation of ion pair, Ca2+ - CoCl42-. A mechanism is proposed to explain the extraction.

  15. Catalytic enantioselective conjugate addition of diethylzinc using NiII-DAIB complexes

    NARCIS (Netherlands)

    Jansen, Johan F.G.A.; Feringa, Bernard

    The conjugate addition of diethylzinc to chalcone, catalyzed by a NiII complex of the chiral aminoalcohol (-)-DAIB, resulted in the formation of (R)-1,3-diphenyl-penta-1-one with enantiomeric excess up to 85%.

  16. Performance of Spent Mushroom Farming Waste (SMFW) Activated Carbon for Ni (II) Removal

    Science.gov (United States)

    Desa, N. S. Md; Ghani, Z. Ab; Talib, S. Abdul; Tay, C. C.

    2016-07-01

    The feasibility of a low cost agricultural waste of spent mushroom farming waste (SMFW) activated carbon for Ni(II) removal was investigated. The batch adsorption experiments of adsorbent dosage, pH, contact time, metal concentration, and temperature were determined. The samples were shaken at 125 rpm, filtered and analyzed using ICP-OES. The fifty percent of Ni(II) removal was obtained at 0.63 g of adsorbent dosage, pH 5-6 (unadjusted), 60 min contact time, 50 mg/L Ni(II) concentration and 25 °C temperature. The evaluated SMFW activated carbon showed the highest performance on Ni(II) removal compared to commercial Amberlite IRC86 resin and zeolite NK3. The result indicated that SMFW activated carbon is a high potential cation exchange adsorbent and suitable for adsorption process for metal removal. The obtained results contribute toward application of developed SMFW activated carbon in industrial pilot study.

  17. Recovery of Cd(II), Co(II) and Ni(II) from Chloride Medium by Solvent Extraction Using CYANEX 923 and CYANEX 272 I

    International Nuclear Information System (INIS)

    Ahmed, M.; El Dessouky, S.I.; El-Nadi, Y.A.; Daoud, J.A.; Saad, E.A.

    2008-01-01

    The paper aims to study the extraction and separation of Cd(II), Co(II) and Ni(II) from their mixtures in hydrochloric acid medium with CYANEX 923 in kerosene. Preliminary investigations showed that only Cd(II) is extracted with CYANEX 923 while Co(II) and Ni(II) are not extracted. Different parameters affecting the extraction of Cd(II) with CYANEX 923 such as hydrochloric acid, hydrogen ion, extractant and metal concentrations, temperature investigations were also investigated. The stoichiometry of the extracted metal species investigated was found to be HCdCl 3 . 2 CYANEX 923. The stripping of the extracted Cd(II) species is obtained with 0.1 M HCl solution. Co(II) was found to be extracted with CYANEX 272 at ph 5.8 leaving Ni(II) in the solution. A developed process for the sequential of Cd(II), Co(II) and Ni(II) from their mixture in hydrochloric acid medium is proposed

  18. DNA binding and biological activity of mixed ligand complexes of Cu(II, Ni(II and Co(II with quinolones and N donor ligand

    Directory of Open Access Journals (Sweden)

    S.M M Akram

    2015-10-01

    Full Text Available  AbstractMixed ligand complexes of  Cu(II, Ni(II and Co(II have been synthesized by using levofloxacin and bipyridyl and characterized using spectral and analytical techniques. The binding behavior of the Ni(II and Cu(II complexes with herring sperm DNA(Hs-DNA were determined using electronic absorption titration, viscometric measurements and cyclic voltammetry measurements. The binding constant calculated  for Cu(II and Ni(II complexes are 2.0 x 104 and 4.0 x 104 M-1 respectively. Detailed analysis reveals that these metal complexes interact with DNA through intercalative binding mode. The nuclease activity of  Cu(II and Ni(II complexes with ct-DNA was carried out using agarose gel electrophoresis technique. The antioxidant activities for the synthesized complexes have been tested and the antibacterial activity for Ni(II complex was also checked.Key words: Intercalation, hypochromism, red shift and  peak potential.

  19. Characterizing Ni(II) hydration in aqueous solution using DFT and EXAFS.

    Science.gov (United States)

    Liu, H Y; Fang, C H; Fang, Y; Zhou, Y Q; Ge, H W; Zhu, F Y; Sun, P C; Miao, J T

    2016-01-01

    In the present work, a detailed investigation of Ni(II) hydration in water solutions was carried out using density functional theory (DFT) and extended X-ray absorption fine structure (EXAFS) spectroscopy. The hydrated characteristics of [Ni(H2O)n](2+) clusters, such as energy parameters, atomic charge distributions, and bond parameters, were explored using DFT with Becke's three-parameter exchange potential and the Lee-Yang-Parr correlation functional (B3LYP). DFT calculations indicated that the preferred structure of the first hydration shell of Ni(II) generally has a coordination number of six and is almost unaffected by the water molecules in the outer solvation shell, whereas the structure of the second solvation shell varies as the hydration proceeds. EXAFS measurements are reported for aqueous NiSO4 and Ni(NO3)2 solutions and the Ni(NO3)2·6H2O crystal. Analysis of the EXAFS spectra of these three systems using a multiparameter fitting procedure showed that, in each case, the first coordination shell consists of six water molecules with a Ni-O coordination distance of 2.04 Å, and that there is no Ni-S or Ni-N coordination in the first shell. There was no evidence of outer-shell SO4(2-) or NO3(-) ions substituting inner-sphere water molecules in NiSO4 and Ni(NO3)2. The characteristics of Ni(II) hydration obtained from DFT calculations agreed well with those obtained experimentally using EXAFS.

  20. Ultraviolet multi-peak emissions of mono-dispersed polymer capped ZnNiO nanocomposites

    International Nuclear Information System (INIS)

    Shijina, K.; Megha, U.; Varghese, George

    2014-01-01

    Nanosized polymer capped ZnNiO composites were synthesized by complexation precipitation method. Crystalline phase and average particle size of the synthesized nanocomposites were investigated by X-ray diffractometer. Average particle size of the samples was also confirmed in scanning electron microscopy (SEM) as well as in reflectance spectra. X-ray diffraction results provide that Ni is incorporated into the ZnO lattice at Zn sites. The diffraction peaks correspond to a hexagonal wurtzite structured ZnNiO. Room temperature reflectance spectra of the nickel substituted ZnO show a bumb around 260 nm for the polymer capped and non-capped samples, which implies higher energy exciton absorption. The reflectance spectra as well as X-ray spectra confirms that the metaloxide nanoparticles are homogeneously distributed in the polymer matrix. Fluorescence properties of the PVP capped ZnNiO at room temperature show intensive multiple peak emissions in the ultra–violet range as well as in blue and green wavelengths, plausibly due to deep level emissions. Raman spectra show the modes, which arise from the vibration of oxygen sub-lattice. -- Highlights: • Multiple peak emission of mono-dispersed ZnNiO nano-particles in UV region. • Ni doping effects the multi-peak emissions. • Peak shifting observed in Raman lines due to metal doping

  1. Spin Crossover in Fe(II)-M(II) Cyanoheterobimetallic Frameworks (M = Ni, Pd, Pt) with 2-Substituted Pyrazines.

    Science.gov (United States)

    Kucheriv, Olesia I; Shylin, Sergii I; Ksenofontov, Vadim; Dechert, Sebastian; Haukka, Matti; Fritsky, Igor O; Gural'skiy, Il'ya A

    2016-05-16

    Discovery of spin-crossover (SCO) behavior in the family of Fe(II)-based Hofmann clathrates has led to a "new rush" in the field of bistable molecular materials. To date this class of SCO complexes is represented by several dozens of individual compounds, and areas of their potential application steadily increase. Starting from Fe(2+), square planar tetracyanometalates M(II)(CN)4(2-) (M(II) = Ni, Pd, Pt) and 2-substituted pyrazines Xpz (X = Cl, Me, I) as coligands we obtained a series of nine new Hofmann clathrate-like coordination frameworks. X-ray diffraction reveals that in these complexes Fe(II) ion has a pseudo-octahedral coordination environment supported by four μ4-tetracyanometallates forming its equatorial coordination environment. Depending on the nature of X and M, axial positions are occupied by two 2X-pyrazines (X = Cl and M(II) = Ni (1), Pd (2), Pt (3); X = Me and M(II) = Ni (4), Pd (5)) or one 2X-pyrazine and one water molecule (X = I and M(II) = Ni (7), Pd (8), Pt (9)), or, alternatively, two distinct Fe(II) positions with either two pyrazines or two water molecules (X = Me and M(II) = Pt (6)) are observed. Temperature behavior of magnetic susceptibility indicates that all compounds bearing FeN6 units (1-6) display cooperative spin transition, while Fe(II) ions in N5O or N4O2 surrounding are high spin (HS). Structural changes in the nearest Fe(II) environment upon low-spin (LS) to HS transition, which include ca. 10% Fe-N distance increase, lead to the cell expansion. Mössbauer spectroscopy is used to characterize the spin state of all HS, LS, and intermediate phases of 1-9 (see abstract figure). Effects of a pyrazine substituent and M(II) nature on the hyperfine parameters in both spin states are established.

  2. Chemical speciation of Pb(II, Cd(II, Hg(II, Co(II, Ni(II, Cu(II and Zn(II binary complexes of l-methionine in 1,2-propanediol-water mixtures

    Directory of Open Access Journals (Sweden)

    M. Padma Latha

    2007-04-01

    Full Text Available Chemical speciation of Pb(II, Cd(II, Hg(II, Co(II, Ni(II, Cu(II and Zn(II complexes of L-methionine in 0.0-60 % v/v 1,2-propanediol-water mixtures maintaining an ionic strength of 0.16 M at 303 K has been studied pH metrically. The active forms of ligand are LH2+, LH and L-. The predominant species detected are ML, MLH, ML2, ML2H, ML2H2 and MLOH. Models containing different numbers of species were refined by using the computer program MINIQUAD 75. The best-fit chemical models were arrived at based on statistical parameters. The trend in variation of complex stability constants with change in the dielectric constant of the medium is explained on the basis of electrostatic and non-electrostatic forces.

  3. Quantum efficiencies of near-infrared emission from Ni2+-doped glass-ceramics

    International Nuclear Information System (INIS)

    Suzuki, Takenobu; Arai, Yusuke; Ohishi, Yasutake

    2008-01-01

    A systematic method to evaluate potentials of Ni 2+ -doped transparent glass-ceramics as a new broadband optical gain media is presented. At first, near-infrared emission of various ceramics were investigated to explore the suitable crystalline phase to be grown in the glass-ceramics. The quantum efficiency of Ni 2+ near-infrared emission estimated by the Struck-Fonger analysis was higher than 95% for spinel-type structure gallate crystals MgGa 2 O 4 and LiGa 5 O 8 at room temperature. Transparent glass-ceramics containing Ni 2+ :LiGa 5 O 8 could be prepared and the quantum efficiency for the glass-ceramics was measured to be about 10%. This value shows a potential of Ni-doped transparent glass-ceramics as a broadband gain media

  4. Facile Pd(II)- and Ni(II)-Catalyzed Isomerization of Terminal Alkenes into 2-Alkenes

    Science.gov (United States)

    Lim, Hwan Jung; Smith, Craig R.; RajanBabu, T. V.

    2009-01-01

    Mono- and 2,2′-di-substituted terminal alkenes can be isomerized into the more stable internal Z- and E- alkenes by treating them with catalytic amounts of [(allyl)PdCl]2 or [(allyl)NiBr]2, a triarylphosphine and silver triflate at room temperature. The isomeric ratio (E:Z) depends on the alkenes, the (E)-isomer being the major one. The reaction is tolerant to a wide variety of functional groups including other reactive olefins. Unlike the more reactive Ir catalysts, monosubstituted alkenes give almost exclusively the 2-alkenes. Direct comparison to two of the best-known catalysts for this process, (Ir(PCy3)3]+ [BPh4]−, and Grubbs Generation II metathesis catalyst) is also reported. PMID:19441793

  5. Thermophysical Properties of Cold- and Vacuum Plasma-Sprayed Cu-Cr-X Alloys, NiAl and NiCrAlY Coatings II: Specific Heat Capacity

    Science.gov (United States)

    Raj, S. V.

    2017-11-01

    Part I of the paper discussed the temperature dependencies of the electrical resistivities, thermal conductivities, thermal diffusivities and total hemispherical emissivities of several vacuum plasma-sprayed (VPS) and cold-sprayed (CS) copper alloy monolithic coatings, VPS NiAl, VPS NiCrAlY, extruded GRCop-84 and as-cast Cu-17(wt.%)Cr-5%Al. Part II discusses the temperature dependencies of the constant-pressure specific heat capacities, C P, of these coatings. The data were empirically regression-fitted with the equation: \\varvec{C}_{P} = {AT}^{4} + {BT}^{3} + {CT}^{2} + DT + \\varvec{E}where T is the absolute temperature and A, B, C, D and E are regression constants. The temperature dependencies of the molar enthalpy, molar entropy and Gibbs molar free energy determined from experimental values of molar specific heat capacity are reported. Calculated values of C P using the Neumann-Kopp (NK) rule were in poor agreement with experimental data. Instead, a modification of the NK rule was found to predict values closer to the experimental data with an absolute deviation less than 6.5%. The specific molar heat capacities for all the alloys did not agree with the Dulong-Petit law, and C P > 3 R, where R is the universal gas constant, were measured for all the alloys except NiAl for which C P < 3 R at all temperatures.

  6. Ferro- to antiferromagnetic crossover angle in diphenoxido- and carboxylato-bridged trinuclear Ni(II)₂-Mn(II) complexes: experimental observations and theoretical rationalization.

    Science.gov (United States)

    Seth, Piya; Figuerola, Albert; Jover, Jesús; Ruiz, Eliseo; Ghosh, Ashutosh

    2014-09-02

    Three new trinuclear heterometallic Ni(II)-Mn(II) complexes have been synthesized using a [NiL] metalloligand, where H2L = N,N'-bis(salicylidene)-1,3-propanediamine. The complexes [(NiL)2Mn(OCnn)2(CH3OH)2]·CH3OH (1), [(NiL)2Mn(OPh)2(CH3OH)2][(NiL)2Mn(OPh)2]·H2O (2), and [(NiL)2Mn(OSal)2(CH3OH)2]·2[NiL] (3) (where OCnn = cinnamate, OPh = phenylacetate, OSal = salicylate) have been structurally characterized. In all three complexes, in addition to the double phenoxido bridge, the two terminal Ni(II) atoms are linked to the central Mn(II) by means of a syn-syn bridging carboxylate, giving rise to a linear structure. Complexes 1 and 2 with Ni-O-Mn angles of 97.24 and 96.43°, respectively, exhibit ferromagnetic interactions (J(Ni-Mn) = +1.38 and +0.50 cm(-1), respectively), whereas 3 is antiferromagnetic (J(Ni-Mn) = -0.24 cm(-1)), having an Ni-O-Mn angle of 98.51°. DFT calculations indicate that there is a clear magneto-structural correlation between the Ni-O-Mn angle and J(Ni-Mn) values, which is in agreement with the experimental results.

  7. Linear Acceleration Emission. II. Power Spectrum

    Science.gov (United States)

    Melrose, D. B.; Luo, Q.

    2009-06-01

    The theory of linear acceleration emission (LAE) is developed for a large amplitude electrostatic wave in which all particles become highly relativistic in much less than a wave period. An Airy-integral approximation is shown to apply near the phases where the electric field passes through zero and the Lorentz factors of all particles have their maxima. The emissivity is derived for an individual particle and is integrated over frequency and solid angle to find the power radiated per particle. The result is different from that implied by the generalized Larmor formula which, we argue, is not valid in this case. We also discuss a mathematical inconsistency that arises when one evaluates the power spectrum by integrating the emissivity over solid angle. The correct power spectrum increases as the 4/3rd power of the frequency at low frequencies, and falls off exponentially above a characteristic frequency. We discuss application of LAE to the emission of high-frequency photons in an oscillating model for pulsars. We conclude that it cannot account for gamma-ray emission, but can play a role in secondary pair creation.

  8. LINEAR ACCELERATION EMISSION. II. POWER SPECTRUM

    International Nuclear Information System (INIS)

    Melrose, D. B.; Luo, Q.

    2009-01-01

    The theory of linear acceleration emission (LAE) is developed for a large amplitude electrostatic wave in which all particles become highly relativistic in much less than a wave period. An Airy-integral approximation is shown to apply near the phases where the electric field passes through zero and the Lorentz factors of all particles have their maxima. The emissivity is derived for an individual particle and is integrated over frequency and solid angle to find the power radiated per particle. The result is different from that implied by the generalized Larmor formula which, we argue, is not valid in this case. We also discuss a mathematical inconsistency that arises when one evaluates the power spectrum by integrating the emissivity over solid angle. The correct power spectrum increases as the 4/3rd power of the frequency at low frequencies, and falls off exponentially above a characteristic frequency. We discuss application of LAE to the emission of high-frequency photons in an oscillating model for pulsars. We conclude that it cannot account for gamma-ray emission, but can play a role in secondary pair creation.

  9. The European Dioxin Emission Inventory. Stage II. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Quass, U.; Fermann, M.; Broeker, G.

    2001-07-01

    For Stage II of the European Dioxin Project the following objectives were set: - Amendment of existing emission data collected for most relevant emission sources in order to reduce uncertainties of emission estimates. Collecting first emission data from countries not yet performing dioxin emission measurement programs. Extending the inventory of dioxin emissions to ambient air produced in Stage I by a complementary study on emissions to land and water. Extending the regional scope of data collection to countries in Central Europe. The report of Stage II of the European Dioxin Project is presented in 3 Volumes. Volume 1 contains an overview on the background and approach of different activities carried out and on the results obtained. These results are put into a broader view regarding the dioxin reduction measures in Europe leading to conclusions and recommendation for future work. Volume 2 of the report contains a detailed presentation of the sub-projects carried out. The chapters of Volume 2 are structured in a similar manner and start with a short summary in order to allow for a fast cross-reading. In the case of the desk-top studies an overview of the main results or statements is given. Regarding emission measurements details on the experimental set-up and the facilities being investigated are presented. Volume 3 contains a re-evaluation of the dioxin emission inventory presented for the most relevant sources types in the Stage I report. New data gathered from the projects of Stage II as well as from independent activities in the European countries are considered for a revision of the 1995 emission estimates. Additionally, based on current trends and activities the PCDD/F emissions for the years 2000 and 2005 are estimated. Finally, an attempt is made to evaluate the PCDD/F emission reduction rates which might be possible to achieve by the year 2005 compared to 1985. (orig.)

  10. Coordination-organometallic hybrid materials based on the trinuclear M(II)-Ru(II) (M=Ni and Zn) complexes: Synthesis, structural characterization, luminescence and electrochemical properties

    Science.gov (United States)

    Pawal, S. B.; Lolage, S. R.; Chavan, S. S.

    2018-02-01

    A new series of trinuclear complexes of the type Ni[R-C6H4Ndbnd CH(O)C6H3Ctbnd CRu(dppe)2Cl]2 (1a-c) and Zn[Rsbnd C6H4Ndbnd CH(O)C6H3Ctbnd CRu(dppe)2Cl]2 (2a-c) have been prepared from the reaction of trans-[RuCl(dppe)2Ctbnd Csbnd C6H3(OH)(CHO)] (1) with aniline, 4-nitroaniline and 4-methoxyaniline (R1-3) in presence of nickel acetate and zinc acetate in CH2Cl2/MeOH (1:1) mixture. The structural properties of the complexes have been characterized by elemental analyses and spectroscopic techniques viz. FTIR, UV-Visible, 1H NMR and 31P NMR spectral studies. The crystal structure and morphology of the hybrid complexes was investigated with the help of X-ray powder diffraction (XRPD), Scanning electron microscopy (SEM) and Transmission electron microscopy (TEM). The thermal properties of 1a-c and 2a-c were studied by thermogravimetric (TG) analysis. The electrochemical behaviour of the complexes reveals that all complexes displayed a quasireversible redox behaviour corresponding to Ru(II)/Ru(III) and Ni(II)/Ni(III) couples for 1a-c and only Ru(II)/Ru(III) couple for 2a-c. All complexes are emissive in solution at room temperature revealing the influence of substituents and solvent polarity on emission properties of the complexes.

  11. Synthesis, Characterization, and Biological Activity of Mn(II, Fe(II, Co(II, Ni(II, Cu(II, Zn(II, and Cd(II Complexes of N-Thiophenoyl-N′-Phenylthiocarbohydrazide

    Directory of Open Access Journals (Sweden)

    M. Yadav

    2013-01-01

    Full Text Available Mn(II, Fe(II, Co(II, Ni(II, Cu(II, Zn(II, and Cd(II complex of N-thiophenoyl -N′-phenylthiocarbohydrazide (H2 TPTH have been synthesized and characterized by elemental analysis, magnetic susceptibility measurements, infrared, NMR, electronic, and ESR spectral studies. The complexes were found to have compositions [Mn(H TPTH2], [Co(TPTH (H2O2], [Ni(TPTH (H2O2], [Cu(TPTH], [Zn(H TPTH], [Cd(H TPTH2], and [Fe(H TPTH2(EtOH]. The magnetic and electronic spectral studies suggest square planar geometry for [Cu(TPTH], tetrahedral geometry for [Zn(TPTH] and [Cd(H TPTH2], and octahedral geometry for rest of the complexes. The infrared spectral studies of the 1 : 1 deprotonated complexes suggest bonding through enolic oxygen, thiolato sulfur, and both the hydrazinic nitrogens. Thus, H2TPTH acts as a binegative tetradentate ligand. H2 TPTH and its metal complexes have been screened against several bacteria and fungi.

  12. Chiral mixed ligand Co(II) and Ni(II) complexes: synthesis and biological activity.

    Science.gov (United States)

    Shivankar, Vitthal S; Thakkar, Narendra V

    2004-01-01

    Chiral mixed ligand (CML) transition metal complexes of the type MQL.2H2O, where M is Co(II)/Ni(II), Q is deprotonated 8-hydroxyquinoline and L is a deprotonated chiral saccharide such as (+)-glucose and (-)-fructose, have been synthesized. The metal complexes have been characterized on the basis of elemental analysis and various physicochemical techniques such as molar conductance, specific rotation measurements, magnetic, spectral and thermal studies. The cup-plate method has been used to study the antibacterial activity of the compounds against some of the pathogenic bacteria such as C. diphtheriae, E. coli, S. typhi, S. dysenteriae, S. aureus and V. cholerae. The antifungal activity of the complexes against some of the pathogenic fungi such as Candida albicans and Aspergillus niger has been studied by the tube dilution method. The results have been compared against those of controls, which were screened simultaneously. The complexes have been screened for acute oral toxicity in albino rats. The method of Litchfield and Wilcoxon has been used to determine the LD50 values.

  13. DFT investigation of Ni(II) adsorption onto MA-DTPA/PVDF chelating membrane in the presence of coexistent cations and organic acids.

    Science.gov (United States)

    Song, Laizhou; Zhao, Xiaodan; Fu, Jie; Wang, Xiuli; Sheng, Yiping; Liu, Xiaowei

    2012-01-15

    Melamine-diethylenetriaminepentaacetic acid/polyvinylidene fluoride (MA-DTPA/PVDF) chelating membrane bearing polyaminecarboxylate groups was used to remove Ni(II) from nickel plating effluents. Adsorption experiments were conducted to study the adsorption of the membrane towards Ni(II) in Ni(II)-Ca(II), Ni(II)-NH(4)(+), Ni(II)-Fe(III) binary systems, and Ni(II)-lactic acid, Ni(II)-succinic acid and Ni(II)-citric acid complex systems. For the ternary nickel plating processes, the effects of 3d transition metals including Fe(II), Co(II), Cu(II) and Zn(II) on Ni(II) adsorption were evaluated. The influences of the aforementioned coexistent cations and organic acids were elucidated by the continuum solvation model (COSMO)-corrected density functional theory (DFT) method. Geometries and complexation energies were analyzed for metal-MA-DTPA and Ni(II)-organic acid complexes. DFT results accord with the experimental data, indicating that DFT is helpful to evaluate the complexation between the membrane and metal cations. The coexistent Ca(II) tends to form more stable complex with MA-DTPA ligand than NH(4)(+) and Fe(III), and can interfere with the formation of Ni(II)-MA-DTPA complex. The complexing sequence of 3d metals with MA-DTPA ligand is Zn(II)). Therefore, both Fe(II) and Cu(II) have the considerable competition with Ni(II). The stabilities of Ni(II)-organic acid complexes follow the order of lactic acidNi(II)-MA-DTPA complex. Copyright © 2011 Elsevier B.V. All rights reserved.

  14. Ni(II immobilization by bio-apatite materials: Appraisal of chemical, thermal and combined treatments

    Directory of Open Access Journals (Sweden)

    Šljivić-Ivanović Marija

    2016-01-01

    Full Text Available Animal bones are natural and rich source of calcium hydroxyapatite (HAP, which was found to be a good sorbent material for heavy metals and radionuclides. Various treatments can reduce the content of bone organic phase and improve sorption properties. In this study, sorption capacities of raw bovine bones (B and samples obtained by chemical treatment with NaOH (BNaOH, by heating at 400 oC (B400 and by combined chemical and thermal treatment (BNaOH+400, were compared, using Ni(II ions as sorbates. Maximum sorption capacities increased in the order BNi(II sorption was found to be complex, with participation of both HAP and organic phase (when present. Sequential extraction analysis was applied for testing the stability of Ni(II ions sorbed by BNaOH+400. Majority of Ni(II was found in residual phase (65% at lower level of sorbent loading, while with the increase of sorbent saturation carbonate fraction became dominant (39 %. According to the results, BNaOH+400 can be utilized in water purification systems. As an apatite based material with low organic content and high efficiency for Ni(II sorption, it is also a good candidate for in-situ soil remediation, particularly at lower contamination levels. [Projekat Ministarstva nauke Republike Srbije, br. III 43009

  15. Kinetic and spectroscopic investigation of CoII, NiII, and N-oxalylglycine inhibition of the FeII/α-ketoglutarate dioxygenase, TauD

    International Nuclear Information System (INIS)

    Kalliri, Efthalia; Grzyska, Piotr K.; Hausinger, Robert P.

    2005-01-01

    Co II , Ni II , and N-oxalylglycine (NOG) are well-known inhibitors of Fe II /α-ketoglutarate (αKG)-dependent hydroxylases, but few studies describe their kinetics and no spectroscopic investigations have been reported. Using taurine/αKG dioxygenase (TauD) as a paradigm for this enzyme family, time-dependent inhibition assays showed that Co II and Ni II follow slow-binding inhibition kinetics. Whereas Ni II -substituted TauD was non-chromophoric, spectroscopic studies of the Co II -substituted enzyme revealed a six-coordinate site (protein alone or with αKG) that became five-coordinate upon taurine addition. The Co II spectrum was not perturbed by a series of anions or oxidants, suggesting the Co II is inaccessible and could be used to stabilize the protein. NOG competed weakly (K i ∼ 290 μM) with αKG for binding to TauD, with the increased electron density of NOG yielding electronic transitions for NOG-Fe II -TauD and taurine-NOG-Fe II -TauD at 380 nm (ε 38 90-105 M -1 cm -1 ). The spectra of the NOG-bound TauD species did not change significantly upon oxygen exposure, arguing against the formation of an oxygen-bound state mimicking an early intermediate in catalysis

  16. SEPARATION OF Fe (III, Cr(III, Cu(II, Ni(II, Co(II, AND Pb(II METAL IONS USING POLY(EUGENYL OXYACETIC ACID AS AN ION CARRIER BY A LIQUID MEMBRANE TRANSPORT METHOD

    Directory of Open Access Journals (Sweden)

    La Harimu

    2010-06-01

    Full Text Available Fe (III, Cr(III, Cu(II, Ni(II, Co(II, and Pb(II  metal ions had been separated using poly(eugenyl oxyacetic acid as an ion carrier by bulk liquid membrane transport method. The effect of pH, polyeugenyl oxyacetic acid ion carrier concentration, nitric acid concentration in the stripping solution, transport time, and metal concentration were optimized. The result showed that the optimum condition for transport of metal ions was at pH 4 for ion Fe(III and at pH 5 for Cr(III, Cu(II, Ni(II, Co(II, and Pb(II ions. The carrier volumes were optimum with concentration of 1 x 10-3 M at 7.5 mL for Cr(III, Cu (IINi(II, Co(II ions and at 8.5 mL for Fe(III and Pb(II ions. The concentration of HNO3 in stripping phase was optimum at 2 M for Fe(III and Cu(II ions, 1 M for Cr(III, Ni(II and Co(II ions, and 0.5 M for Pb(II ion. The optimum transport times were 36 h for Fe(III and Co(II ions, and 48 h for Cr(III, Cu (II, Ni(II, and Pb(II ions. The concentration of metal ions accurately transported were 2.5 x 10-4 M for Fe(III and Cr(III ions, and 1 M for Cu (II, Ni(II, Co(II, and Pb(II ions. Compared to other metal ions the transport of Fe(III was the highest with selectivity order of Fe(III > Cr(III > Pb(II > Cu(II > Ni(II > Co(II. At optimum condition, Fe(III ion was transported through the membrane at 46.46%.   Keywords: poly(eugenyl oxyacetic acid, transport, liquid membrane, Fe (III, Cr(III, Cu(II, Ni(II, Co(II, and Pb(II ions

  17. Airborne radioactive emission control technology. Volume II

    International Nuclear Information System (INIS)

    Skoski, L.; Berlin, R.; Corby, D.; Clancy, J.; Hoopes, G.

    1980-03-01

    This report reviews the current and future control technology for airborne emissions from a wide variety of industries/facilities, including uranium mining and milling, other nuclear fuel cycle facilities, other NRC-licensed and DOE facilities, fossil fuel facilities, selected metal and non-metal extraction industries, and others. Where specific radioactivity control technology is lacking, a description of any existing control technology is given. Future control technology is assessed in terms of improvements to equipment performance and process alterations. A catalogue of investigated research on advanced control technologies is presented

  18. Laser operation by dissociation of metal complexes. II - New transitions in Cd, Fe, Ni, Se, Sn, Te, V, and Zn

    Science.gov (United States)

    Chou, M. S.; Cool, T. A.

    1977-01-01

    The reported investigation is a continuation of a study conducted by Chou and Cool (1976). The experimental results discussed are partly related to laser transitions in Cd(I), Cd(II), and Zn(II). Laser transitions in Fe(I), Ni(I), Sn(I), Te(I), and V(I) are also considered along with the observation of a laser pulse with two peaks in connection with the study of laser transitions in Se(I). Experiments related to prospective visible laser operation in thallium at 6550 and 6714 are also discussed, giving attention to spontaneous emission measurements at 6550 and 5350 A, the effects of additive molecules, and laser cavity experiments at 6550 and 6714 A.

  19. SYNTHESIS, MAGNETIC AND SPECTROSCOPIC STUDIES of Ni(II ...

    African Journals Online (AJOL)

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    magnetic moment for the Cu(II) complex is 1.9 B.M. which within the expected value for one electron. Furthermore, the complex is non-electrolyte as the molar conductance was found to be at 0.87 ohm-1 cm2 mol-1 in 10-3 M in DMSO [5, 11, 16-18]. Finally, the diamagnetic Zn(II) and Cd(II) complexes show absorption bands ...

  20. Ni(II) and Cu(II) removal from aqueous solution by a heavy metal-resistance bacterium: kinetic, isotherm and mechanism studies.

    Science.gov (United States)

    Zhang, Haikun; Hu, Xiaoke; Lu, Hong

    2017-08-01

    The potentiality of a heavy metal-resistance bacterium Acinetobacter sp. HK-1 for removing Ni(II) and Cu(II) ions from aqueous solution and the biosorption mechanism were investigated in this study. The effects of pH, contact time and Ni(II)/Cu(II) concentration on the adsorption process were evaluated and the maximum biosorption capacity of strain HK-1 was found to be 56.65 mg/g for Ni(II) and 157.2 mg/g for Cu(II), respectively. The experimental kinetic data fit well with the pseudo-second-order model (R 2 > 0.98) and the biosorption process was best explained by the Langmuir-Freundlich dual model (R 2 > 0.97). The morphologies of HK-1 before and after adsorption in a Ni(II)/Cu(II) supplemented system were compared using a scanning electron microscope. After adsorption, the valence state of Ni(II)/Cu(II) was not changed and the formation of nickel/copper phosphate was observed using X-ray photoelectron spectroscopy (XPS) and X-ray diffraction. The results of Fourier transform infrared spectroscopy and XPS further indicated that amine, phosphate and carboxyl groups were involved in the biosorption process. Cu(II) biosorption by Acinetobacter sp. was firstly reported. Based on the above results, it can be concluded that Acinetobacter sp. HK-1 has a promising application in Ni(II) and Cu(II) ion removal from industrial wastewater.

  1. Study of the kinetics of the transport of Cu(II), Cd(II) and Ni(II) ions through a liquid membrane.

    Science.gov (United States)

    Granado-Castro, María D; Galindo-Riaño, María D; Domínguez-Lledó, F C; Díaz-López, C; García-Vargas, M

    2008-06-01

    The coupled transport of Cu(II), Cd(II) and Ni(II) ions through a bulk liquid membrane (BLM) containing pyridine-2-acetaldehyde benzoylhydrazone (2-APBH) as carrier dissolved in toluene has been studied. Once the optimal conditions of extraction of each metal were established, a comparative study of the transport kinetics for these metals was performed by means of a kinetic model involving two consecutive irreversible first-order reactions. The kinetic parameters (apparent rate constants of the metal extraction and re-extraction reactions (k(1), k(2)), the maximum reduced concentration of the metal in the liquid membrane (R(o)max), the time of the maximum value of R(o)(t(max)) and the maximum entry and exit fluxes of the metal through the liquid membrane (J(f)max and J(s)max) of the extraction and stripping reactions were evaluated and results showed good agreement between experimental data and theoretical predictions. Complete transport through the membrane took place according to the following order: Cd(II)>Cu(II)>Ni(II), with similar kinetic parameters obtained for Cu(II) and Cd(III). The transport behaviour of Ni(II) was different to that of Cu(II) and Cd(III), probably due to the different stoichiometry of the nickel complex compared to those of the other metal ions and the different chemical conditions required for its formation. The influence of the sample salinity on the transport kinetics was studied. k(1) values decreased slightly when the feed solution salinity was increased for Cu(II) and Ni(II), but not for Cd(II). Values of k(2) were practically unaffected. The proposed BLM was applied to the preconcentration and separation of metal ions (prior to their determination) in water samples with different saline matrices (CRM, river water and seawater), and good agreement with the certified values was obtained.

  2. Characterization and biological studies on Co(II), Ni(II) and Cu(II) complexes of carbohydrazones ending by pyridyl ring

    Science.gov (United States)

    Abu El-Reash, G. M.; El-Gammal, O. A.; Ghazy, S. E.; Radwan, A. H.

    2013-03-01

    The chelating behavior of ligands based on carbohydrazone core modified with pyridine end towards Co(II), Ni(II) and Cu(II) ions have been examined. The ligands derived from the condensation of carbohydrazide with 2-acetylpyridine (H2APC) and 4-acetylpyridine (H2APEC). The 1H NMR, IR data and the binding energy calculations of H2APC revealed the presence of two stereoisomers syn and anti in the solid state and in the solution. The 1H NMR, IR data and the binding energy calculations confirmed the presence of H2APEC in one keto form only in the solid state and in the solution. The spectroscopic data confirmed that H2APC behaves as a monobasic pentadentate in Co(II) and Cu(II) complexes and as mononegative tetradentate in Ni(II) complex. On the other hand, H2APEC acts as a mononegative tridentate in Co(II) complex, neutral tridentate in Ni(II) complex and neutral bidentate in Cu(II) complex. The electronic spectra and the magnetic measurements of complexes as well as the ESR of the copper complexes suggested the octahedral geometry. The bond length and bond angles were evaluated by DFT method using material studio program. The thermal behavior and the kinetic parameters of degradation were determined using Coats-Redfern and Horowitz-Metzger methods. The antioxidant (DDPH and ABTS methods), anti-hemolytic and in vitro Ehrlich ascites of the compounds have been screened.

  3. Benzothiazolylazo derivatives of some β-dicarbonyl compounds and their Cu(II, Ni(II and Zn(II complexes

    Directory of Open Access Journals (Sweden)

    KRISHNANNAIR KRISHNANKUTTY

    2010-05-01

    Full Text Available The coupling of diazotized 2-aminobenzothiazole with 1,3-dicar-bonyl compounds (benzoylacetone, methyl acetoacetate and acetoacetanilide yielded a new series of tridentate ligand systems (HL. Analytical, IR, 1H--NMR, 13C-NMR and mass spectral data indicated that the compounds exist in the intramolecularly hydrogen bonded azo-enol tautomeric form in which one of the carbonyl groups of the dicarbonyl moiety had enolised and hydrogen bonded to one of the azo nitrogen atoms. The compounds formed stable complexes with Ni(II, Cu(II and Zn(II ions. The Cu(II complexes conform to [CuL(OAc] stoichiometry while the Ni(II and Zn(II complexes are in agreement with [ML2] stoichiometry. Analytical, IR, 1H-NMR, 13C-NMR and mass spectral data of the complexes are consistent with the replacement of the chelated enol proton of the ligand with a metal ion, thus leading to a stable six-membered chelate ring involving a cyclic nitrogen, one of the azo nitrogens and the enolate oxygen. The Zn(II chelates are diamagnetic while Cu(II and Ni(II complexes showed a normal paramagnetic moment.

  4. Application of [sup 57]Fe emission Moessbauer spectroscopy to the investigation of the physico-chemical consequences of the double radioactive decay [sup 57]Ni[yields][sup 57]Co[yields][sup 57]Fe in the solid state

    Energy Technology Data Exchange (ETDEWEB)

    Devillers, M.; Ladriere, J. (Univ. Catholique de Louvain, Louvain-la-Neuve (Belgium). Lab. de Chimie Inorganique et Nucleaire)

    1994-04-01

    [sup 57]Fe emission Mossbauer spectroscopy is shown to be a useful technique for investigating the cumulative recoil and Auger after-effects associated with the double electron capture decay, [sup 57]Ni[yields][sup 57]Co''->[sup 57]Fe, in the solid state. Experimental results collected in several types of nickel-containing matrices are surveyed: conducting materials (Ni metal), ionic compounds with monoatomic ligands [potassium trifluoronickelate (II)] and coordination compounds with polyatomic ligands (carboxylates). (Author).

  5. Synthesis and characterization of heterobimetallic complexes of the type [Cu(pn2][MCl4] where M = Co(II, Ni(II, Cu(II, Zn(II, Cd(II, and Hg(II

    Directory of Open Access Journals (Sweden)

    Seema Yadav

    2016-11-01

    Full Text Available A series of new bimetallic transition metal complexes of the type [Cu(pn2] [MCl4] have been synthesized (where M = Co(II, Ni(II, Cu(II, Zn(II, Cd(II and Hg(II, pn = 1,3-diaminopropane and characterized by elemental analysis, molar conductance, TGA, IR and electronic spectra. All the compounds are 1:1 electrolyte in DMF. The Cu(II ion is square-planar while metal ions in the anionic moiety acquire their usual tetrahedral arrangement. On the basis of these studies it is concluded that anionic moiety is electrically stabilized by its cationic counterpart.

  6. Simulations on Nickel target preparation and separation of Ni(II)-Cu(II) matrix for production of radioisotope 64Cu

    International Nuclear Information System (INIS)

    Sunarhadijoso Soenarjo; Wira Y Rahman; Sriyono; Triyanto

    2011-01-01

    The simulations on Nickel target preparation and separation of Ni(II)-Cu(II) matrix has been carried out as a preliminary study for production of medical radioisotope Cu-64 based on nuclear reaction of 64 Ni (p,n) 64 Cu. The nickel target preparation was performed by means of electroplating method using acidic solution of nickel chloride - boric acid mixture and basic solution of nickel sulphate - nickel chloride mixture on a silver - surfaced-target holder. The simulated solution of Ni(II) - Cu(II) matrix was considered as the solution of post-proton-irradiated nickel target containing both irradiated nickel and radioactive copper, but in the presented work the proton irradiation of nickel target was omitted, while the radioactive copper was originally obtained from neutron irradiation of CuO target. The separation of radioactive copper from the nickel target matrix was based on anion exchange column chromatography in which the radiocopper was conditioned to form anion complex CuCl 4 2- and retained on the column while the nickel was kept in the form of Ni 2+ cation and eluted off from the column. The retained radioactive copper was then eluted out the column in the condition of dilute HCl changing back the copper anion complex into Cu 2+ cation. It was found that the electroplating result from the acidic solution was more satisfied than that from the basic solution. By conditioning the matrix solution at HCl 6 M, the radioactive copper was found in the forms of Cu 2+ and CuCl 4 2- while the nickel was totally in the form of Ni 2+ . In the condition of HCl 9 M, the radioactive copper was mostly in the form of CuCl 4 2- while the nickel was found as both Ni 2+ and NiCl 4 2- . The best condition of separation was in HCl 8 M in which the radioactive copper was mostly in the form of CuCl 4 2- while the nickel was mostly in the form of Ni 2+ . The retained CuCl 4 2- was then changed back into Cu 2+ cation form and eluted out the column by using HCl 0.05 M. The

  7. Adsorption of Cu(II), Cd(II) and Ni(II) ions by cross-linked magnetic chitosan-2-aminopyridine glyoxal Schiff's base.

    Science.gov (United States)

    Monier, M; Ayad, D M; Abdel-Latif, D A

    2012-06-01

    The adsorption of Cu(II), Cd(II) and Ni(II) ions from aqueous solution by cross-linked magnetic chitosan-2-aminopyridine glyoxal Schiff's base resin (CSAP) was studied in a batch adsorption system. Cu(II), Cd(II) and Ni(II) removal is pH dependent and the optimum adsorption was observed at pH 5.0. The adsorption was fast with estimated initial rate of 2.7, 2.4 and 1.4 mg/(g min) for Cu(2+), Cd(2+) and Ni(2+) respectively. The adsorption data could be well interpreted by the Langmuir, Freundlich and Temkin model. The maximum adsorption capacities obtained from the Langmuir model were 124±1, 84±2 and 67±2 mg g(-1) for Cu(2+), Cd(2+) and Ni(2+) respectively. The adsorption process could be described by pseudo-second-order kinetic model. Thermodynamic parameters revealed the feasibility, spontaneity and exothermic nature of adsorption. The sorbents were successfully regenerated using EDTA and HCl solutions. Copyright © 2012 Elsevier B.V. All rights reserved.

  8. Artificial neural networks study of the catalytic reduction of resazurin: stopped-flow injection kinetic-spectrophotometric determination of Cu(II) and Ni(II)

    International Nuclear Information System (INIS)

    Magni, Diana M.; Olivieri, Alejandro C.; Bonivardi, Adrian L.

    2005-01-01

    An artificial neural network (ANN) procedure was used in the development of a catalytic spectrophotometric method for the determination of Cu(II) and Ni(II) employing a stopped-flow injection system. The method is based on the catalytic action of these ions on the reduction of resazurin by sulfide. ANNs trained by back-propagation of errors allowed us to model the systems in a concentration range of 0.5-6 and 1-15 mg l -1 for Cu(II) and Ni(II), respectively, with a low relative error of prediction (REP) for each cation: REP Cu(II) = 0.85% and REP Ni(II) = 0.79%. The standard deviations of the repeatability (s r ) and of the within-laboratory reproducibility (s w ) were measured using standard solutions of Cu(II) and Ni(II) equal to 2.75 and 3.5 mg l -1 , respectively: s r [Cu(II)] = 0.039 mg l -1 , s r [Ni(II)] = 0.044 mg l -1 , s w [Ni(II)] = 0.045 mg l -1 and s w [Ni(II)] = 0.050 mg l -1 . The ANNs-kinetic method has been applied to the determination of Cu(II) and Ni(II) in electroplating solutions and provided satisfactory results as compared with flame atomic absorption spectrophotometry method. The effect of resazurin, NaOH and Na 2 S concentrations and the reaction temperature on the analytical sensitivity is discussed

  9. Elaborated studies for the ligitional behavior of thiouracil derivative towards Ni(II), Pd(II), Pt(IV), Cu(II) and UO2 ² ions.

    Science.gov (United States)

    Abou-Melha, Khlood Saad

    2012-11-01

    A synthesis of new thiouracil derivative was carried out and deliberately investigated. A new series of complexes was prepared using Ni(II), Pd(II), Pt(IV), Cu(II) and UO(2)(+2) ions. IR spectral data proposed the coordination mod of the ligand towards each metal ion and displays the binegative pentadentate mod as the maximum mod of coordination obtained with Ni(II) and Cu(II) complexes. (1)HNMR spectrum of UO(2)(+2) complex in comparing with the free ligand spectrum supports the binegative appearance of the coordinated ligand through the ionization of CO and CS groups. The electronic spectral data as well as the magnetic moment measurements are coincide with each others to propose the square-planar geometry with Ni(II), Pd(II) and Cu(II) complexes and octahedral geometry with the others. ESR spectrum of Cu(II) complex displays axially symmetric g tensor parameters with g(11)>g(⊥)>2.0023 indicating that the [Formula: see text] orbital as a ground state with the square-planar geometry. The TG analysis for all isolated complexes were carried out to assert about the presence of water molecules physically or chemically attached with the central atom. The biological study was carried out against different microorganisms as gram negative, gram positive and fungi. The comparable data display the relative priority of Ni(II) complex in comparing with others against all organisms but, the other complexes display activity by the same with the free ligand. Copyright © 2012 Elsevier B.V. All rights reserved.

  10. CATALYTIC ENANTIOSELECTIVE CONJUGATE ADDITION OF DIETHYLZINC USING NI(II) DAIB COMPLEXES

    NARCIS (Netherlands)

    JANSEN, JFGA; FERINGA, BL

    The conjugate addition of diethylzinc to chalcone, catalyzed by a NiII complex of the chiral amino-alcohol (-)-DAIB, resulted in the formation of (R)-1,3-diphenyl-penta-1-one with enantiomeric excess up to 85%.

  11. Characterization and Utilization of Tannin Extract for the Selective Adsorption of Ni (II Ions from Water

    Directory of Open Access Journals (Sweden)

    Priya Meethale Kunnambath

    2015-01-01

    Full Text Available The current paper studies the preparation of a new tannin gel from Acacia nilotica for water purification and waste water remediation. Design of experiments is used for optimizing the tannin gel using tannin extract (Taguchi method with formaldehyde in the assistance of microwave (TGAN by the help of iodine number. The feasible combinations were tested in the removal of nickel from simulated and river water. In this study, the effect of adsorbent dosage, pH, and initial metal concentration on Ni (II biosorption on modified Acacia nilotica tannin gel (TGAN was investigated. Tannin gel was characterized by SEM, FTIR, XRD, and EDAX. The kinetic data was tested using pseudo-first-order, pseudo-second-order, and intraparticle diffusion model. The results suggested that the pseudo-second-order model (R2 > 0.998 was the best choice among all the kinetic models describing the adsorption behavior of Ni (II onto TGAN. Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich adsorption models were used to represent the equilibrium data. The best interpretation for the experimental data was given by the Langmuir isotherm and the maximum adsorption capacity 250 mg g−1 of Ni (II was obtained at pH 5.04 at 296 K. Adsorption of Ni (II onto TGAN is confirmed qualitatively by the use of atomic absorption spectroscopy. The BOD and COD values are considerably reduced after adsorption.

  12. DNA binding and cleavage activity of a structurally characterized Ni(II)

    Indian Academy of Sciences (India)

    1375–1381. c Indian Academy of Sciences. DOI 10.1007/s12039-015-0900-4. DNA binding and cleavage activity of a structurally characterized Ni(II). Schiff base complex. SARAT CHANDRA KUMARa, ABHIJIT PALa, MERRY MITRAa,. V M MANIKANDAMATHAVANb, CHIA -HER LINc, BALACHANDRAN UNNI NAIRb,∗.

  13. Adsorption of Ni(II) onto Chemically Modified Spent Grated Coconut (Cocos Nucifera)

    Science.gov (United States)

    Hamzah, F. I.; Khalid, K.; Hanafiah, M. A. K. M.

    2017-06-01

    A new adsorbent of plant waste origin from coconut processing food factory was explored for removing Ni(II) from aqueous solutions. Several parameters such as pH, dosage, concentration and contact time were studied to obtain optimum conditions for treatment of Ni(II) contaminated wastewater. Spent grated coconut (Cocos nucifera) treated with sulfuric acid (SSGC) showed good adsorption capacity for Ni(II) ion. The amount adsorbed was affected by solution pH with the highest value achieved at pH 5. Other optimum conditions found were; dosage of 0.02 g, and 60 min of equilibrium time. Ni(II) adsorption obeyed the pseudo-second order kinetic model which suggested that chemisorption mechanism occurred in the adsorption process. The equilibrium data presented a better fitting to the Langmuir isotherm model, an indication that monolayer adsorption occurred onto a homogeneous surface. The maximum adsorption capacity, qmax was 97.09 mg g-1, thus SSGC can be classified as good and comparable with other plant waste adsorbents.

  14. Azadirachta indica leaf powder as a biosorbent for Ni(II) in aqueous medium

    Energy Technology Data Exchange (ETDEWEB)

    Bhattacharyya, Krishna G., E-mail: krishna2604@sify.com [Department of Chemistry, Gauhati University, Guwahati 781014, Assam (India); Sarma, Jyotirekha [Department of Chemistry, Gauhati University, Guwahati 781014, Assam (India); Sarma, Arunima [Department of Chemistry, Morigaon College, Morigaon 782105, Assam (India)

    2009-06-15

    Azadirachta indica leaves are converted to a fine powder for use as a biosorbent for the removal of metal ions in aqueous solution. In this work, the adsorptive interactions between Ni(II) and the powder were studied under a variety of conditions involving variations in pH, Ni(II) concentration, biosorbent amount, interaction time and temperature, all in single batch processes. The experimental data have been interpreted on the basis of existing mathematical models of equilibrium kinetics and thermodynamics. The biosorption of Ni(II) increased in the pH range of 2.0-5.0 with {approx}92.6% adsorption at pH 5.0 for the highest amount of the biosorbent (4 g/L). The biosorption followed second-order kinetics and intra-particle diffusion was likely to have significant influence in controlling the process. The Langmuir monolayer adsorption capacity varied from 2.4 to 9.1 mg/g and the equilibrium coefficient from 1.09 to 2.78 L/g with strong indication that the Ni(II) ions were held on the biosorbent surface by formation of an adsorption complex. The thermodynamic parameters showed the process to be exothermic in nature supported by appropriate ranges of values of enthalpy change, entropy change and Gibbs energy change.

  15. A mixed Ni(II) ionic complex containing V-shaped water trimer ...

    Indian Academy of Sciences (India)

    A mixed Ni(II) ionic complex containing V-shaped water trimer: Synthesis, spectral, structural and ... bonding interaction between three lattice water molecule forms a V-shaped trimer (H2O)3 which gives rise to a. 1-D polymeric structure in the ... with organic ligands should be handled with care as they can cause explosion.

  16. Six, Seven or Eight Coordinate Fe(II) , Co(II) or Ni(II) Complexes of Amide-Appended Tetraazamacrocycles for ParaCEST Thermometry.

    Science.gov (United States)

    Olatunde, Abiola O; Bond, Christopher J; Dorazio, Sarina J; Cox, Jordan M; Benedict, Jason B; Daddario, Michael D; Spernyak, Joseph A; Morrow, Janet R

    2015-12-07

    Fe(II) , Co(II) and Ni(II) complexes of two tetraazamacrocycles (1,4,8,11-tetrakis(carbamoylmethyl)-1,4,8,11-tetraazacyclotetradecane (L1) and 1,4,7,10-tetrakis(carbamoylmethyl)-1,4,7,10-tetraazacyclododecane (L2) show promise as paraCEST agents for registration of temperature (paraCEST=paramagnetic chemical exchange saturation transfer). The Fe(II) , Co(II) and Ni(II) complexes of L1 show up to four CEST peaks shifted ≤112 ppm, whereas analogous complexes of L2 show only a single CEST peak at ≤69 ppm. Comparison of the temperature coefficients (CT ) of the CEST peaks of [Co(L2)](2+) , [Fe(L2)](2+) , [Ni(L1)](2+) and [Co(L1)](2+) showed that a CEST peak of [Co(L1)](2+) gave the largest CT (-0.66 ppm (o) C(-1) at 4.7 T). NMR spectral and CEST properties of these complexes correspond to coordination complex symmetry as shown by structural data. The [Ni(L1)](2+) and [Co(L1)](2+) complexes have a six-coordinate metal ion bound to the 1-, 4-amide oxygen atoms and four nitrogen atoms of the tetraazamacrocycle. The [Fe(L2)](2+) complex has an unusual eight-coordinate Fe(II) bound to four amide oxygen atoms and four macrocyclic nitrogen atoms. For [Co(L2)](2+) , one structure has seven-coordinate Co(II) with three bound amide pendents and a second structure has a six-coordinate Co(II) with two bound amide pendents. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  17. Fe II emission lines. I - Chromospheric spectra of red giants

    Science.gov (United States)

    Judge, P. G.; Jordan, C.

    1991-01-01

    A 'difference filtering' algorithm developed by Ayers (1979) is used to construct high-quality high-dispersion long-wavelength IUE spectra of three giant stars. Measurements of all the emission lines seen between 2230 and 3100 A are tabulated. The emission spectrum of Fe II is discussed in comparison with other lines whose formation mechanisms are well understood. Systematic changes in the Fe II spectrum are related to the different physical conditions in the three stars, and examples are given of line profiles and ratios which can be used to determine conditions in the outer atomspheres of giants. It is concluded that most of the Fe II emission results from collisional excitation and/or absorption of photospheric photons at optical wavelengths, but some lines are formed by fluorescence, being photoexcited by other strong chromospheric lines. Between 10 and 20 percent of the radiative losses of Fe II arise from 10 eV levels radiatively excited by the strong chromospheric H Ly-alpha line.

  18. Thermophysical Properties of Cold and Vacuum Plasma Sprayed Cu-Cr-X Alloys, NiAl and NiCrAlY Coatings. Part 1; Electrical and Thermal Conductivity, Thermal Diffusivity, and Total Hemispherical Emissivity

    Science.gov (United States)

    Raj, S. V.

    2017-01-01

    This two-part paper reports the thermophysical properties of several cold and vacuum plasma sprayed monolithic Cu and Ni-based alloy coatings. Part I presents the electrical and thermal conductivity, thermal diffusivity, and total hemispherical emissivity data while Part II reports the specific heat capacity data for these coatings. Metallic copper alloys, stoichiometric NiAl and NiCrAlY coatings were fabricated by either the cold sprayed or the vacuum plasma spray deposition processes for thermal property measurements between 77 and 1223 K. The temperature dependencies of the thermal conductivities, thermal diffusivities, electrical conductivities and total hemispherical emissivities of these cold and vacuum sprayed monolithic coatings are reported in this paper. The electrical and thermal conductivity data correlate reasonably well for Cu-8%Cr-1%Al, Cu-23%Cr-5%Al and NiAl in accordance with the Wiedemann-Franz (WF) law although a better fit is obtained using the Smith-Palmer relationship. The Lorentz numbers determined from the WF law are close to the theoretical value.

  19. Investigation on the spatial evolution of the emission spectra in laser-induced Ni plasmas

    International Nuclear Information System (INIS)

    Du Chuanmei; Xu Ying; Zhang Mingxu

    2012-01-01

    In this paper, the spatial resolved emission spectrum of Ni atom in laser induced Ni plasma is measured in the wavelength region from 350 nm to 600 nm. The spatial evolution of the relative intensities and the Stark broadening of the 385.83 nm emission spectrum lines are also obtained. It is shown that Stark broadening and intensity of the spectrum lines increases firstly to its maximum and then de- creases along the direction of laser beam when the distance from the target surface is in the range from 0 to 2.5 mm. The maximum value of Stark broadening and relative intensity of the spectrum lines appear at 1.5 mm from the target surface. (authors)

  20. Synthesis and Antimicrobial Studies Of Mn(II), Co(II), Ni(Ii), Zn(II) and ...

    African Journals Online (AJOL)

    2017-08-20

    Aug 20, 2017 ... dentate ligands capable of forming very stable complexes with transition metals Tetradentate. Schiff bases with N2O2 donor atoms are well known to coordinate with various transition metal ions (Costamagna et al,. 2000). The complexes of transition metal(II) which involves derivatives of amino acids and.

  1. Ni (II) adsorption onto Chrysanthemum indicum: Influencing factors, isotherms, kinetics, and thermodynamics.

    Science.gov (United States)

    Vilvanathan, Sowmya; Shanthakumar, S

    2016-10-02

    The study explores the adsorption potential of Chrysanthemum indicum biomass for nickel ion removal from aqueous solution. C. indicum flowers in raw (CIF-I) and biochar (CIF-II) forms were used as adsorbents in this study. Batch experiments were conducted to ascertain the optimum conditions of solution pH, adsorbent dosage, contact time, and temperature for varying initial Ni(II) ion concentrations. Surface area, surface morphology, and functionality of the adsorbents were characterized by Brunauer, Emmett, and Teller (BET) surface analysis, scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and Fourier transform infrared spectroscopy (FTIR). Adsorption kinetics were modeled using pseudo-first order, pseudo-second order, Elovich, intraparticle diffusion, Bangham's, and Boyd's plot. The equilibrium data were modeled using Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich (D-R) isotherm models. Experimental data provided the best fit to pseudo-second-order kinetic model and Langmuir isotherm model for the adsorption of Ni(II) ion on both CIF-I and CIF-II with maximum adsorption capacities of 23.97 and 44.02 mg g(-1), respectively. Thermodynamic analysis of the data proved the process to be spontaneous and endothermic in nature. Desorption studies were conducted to evaluate the possibility of reusing the adsorbents. Findings of the present study provide substantial evidence for the use of C. indicum flower as an eco-friendly and potential adsorbent for the removal of Ni(II) ions from aqueous solution.

  2. Molecular and supramolecular characterization of Ni(II)/losartan hydrophobic nanoprecipitate

    Science.gov (United States)

    Nascimento, Lorrayne O.; Goulart, Pedro P.; Correa, Jéssyca L.; Abrishamkar, Afshin; Da Silva, Jeferson G.; Mangrich, Antonio S.; de França, Amanda A.; Denadai, Ângelo M. L.

    2014-09-01

    In this work, a contribution to understanding of the formation of metal(II)/losartan hydrophobic nanoprecipitate is reported. A Ni(II)/Los system was prepared and characterized in solid state and in solution. Solubility studies confirmed the formation of hydrophobic precipitate. Obtained spectroscopic data suggest a sort of coordination between tetrazolic ring as well as OH, and a D4h geometry around the nickel cation. Thermodynamic studies demonstrated that complexation is a stepwise process, with equal enthalpic and entropic contributions for free energy of complexation. DLS and zeta potential titrations indicate the formation of stable nanoparticles of size and charge dependent on the molar ratio. Finally, rheological studies demonstrate a Bingham plastic behavior for Ni(II)/Los suspension.

  3. Acoustic emission monitoring of activation behavior of LaNi5 hydrogen storage alloy

    Directory of Open Access Journals (Sweden)

    Igor Maria De Rosa, Alessandro Dell'Era, Mauro Pasquali, Carlo Santulli and Fabrizio Sarasini

    2011-01-01

    Full Text Available The acoustic emission technique is proposed for assessing the irreversible phenomena occurring during hydrogen absorption/desorption cycling in LaNi5. In particular, we have studied, through a parametric analysis of in situ detected signals, the correlation between acoustic emission (AE parameters and the processes occurring during the activation of an intermetallic compound. Decreases in the number and amplitude of AE signals suggest that pulverization due to hydrogen loading involves progressively smaller volumes of material as the number of cycles increases. This conclusion is confirmed by electron microscopy observations and particle size distribution measurements.

  4. Activated carbon prepared from biomass as adsorbent: elimination of Ni(II) from aqueous solution.

    Science.gov (United States)

    Kadirvelu, K; Senthilkumar, P; Thamaraiselvi, K; Subburam, V

    2002-01-01

    Activated carbon (AC) prepared from waste Parthenium was used to eliminate Ni(lI) from aqueous solution by adsorption. Batch mode adsorption experiments are carried out, by varying contact time, metal ion concentration, carbon concentration, pH and desorption to assess kinetic and equilibrium parameters. They allowed initial adsorption coefficient, adsorption rate constant and maximum adsorption capacities to be computed. The adsorption data were modeled by using both Langmuir and Freundlich classical adsorption isotherms. The adsorption capacity (Q0) calculated from the Langmuir isotherm was 54.35 mg Ni(II)/g of AC at initial pH of 5.0 and 20 degrees C, for the particle size 250-500 microm. Increase in pH from 2 to 10 increased percent removal of metal ion. The regeneration by HCl of Ni(II)-saturated carbon by HCl, allowed suggestion of an adsorption mechanism by ion-exchange between metal ion and H+ ions on the AC surfaces. Quantitative recovery of Ni(II) was possible with HCl.

  5. Synthesis, magnetic and spectroscopic studies of Ni(II, Cu(II, Zn(II and Cd(II complexes of a newly Schiff base derived from 5-bromo-2-hydroxybezylidene-3,4,5-trihydroxybenzohydrazide

    Directory of Open Access Journals (Sweden)

    Mahmood A. Abdullah

    2012-12-01

    Full Text Available A new hydrazide Shiff base ligand GHL1 (5-bromo-2-hydroxybezylidene-3,4,5-trihydroxybenzohydrazide was prepared by refluxing of trihydroxybenzhydrazide with an ethanolic of 5-bromo-2-hydroxybenzaldehyde. The ligand reacted with Ni(II, Cu(II, Zn(II and Cd(II (acetate salts. All the complexes were characterized by elemental analysis, molar conductivity, TGA, UV-Vis and FT-IR spectral studies. All the complexes have octahedral geometry except Ni(II complex which has tetrahedral geometry.DOI: http://dx.doi.org/10.4314/bcse.v26i1.10

  6. Computational studies of a paramagnetic planar dibenzotetraaza[14]annulene Ni(II) complex.

    Science.gov (United States)

    Rabaâ, Hassan; Khaledi, Hamid; Olmstead, Marilyn M; Sundholm, Dage

    2015-05-28

    A square-planar Ni(II) dibenzotetraaza[14]annulene complex substituted with two 3,3-dimethylindolenine groups in the meso positions has recently been synthesized and characterized experimentally. In the solid-state, the Ni(II) complex forms linear π-interacting stacks with Ni···Ni separations of 3.448(2) Å. Measurements of the temperature dependence of the magnetic susceptibility revealed a drastic change in the magnetic properties at a temperature of 13 K, indicating a transition from low-to-high spin states. The molecular structures of the free-base ligand, the lowest singlet, and triplet states of the monomer and the dimer of the Ni complex have been studied computationally using density functional theory (DFT) and ab initio correlation levels of theory. In calculations at the second-order Møller-Plesset (MP2) perturbation theory level, a large energy of 260 kcal mol(-1) was obtained for the singlet-triplet splitting, suggesting that an alternative explanation of the observed magnetic properties is needed. The large energy splitting between the singlet and triplet states suggests that the observed change in the magnetism at very low temperatures is due to spin-orbit coupling effects originating from weak interactions between the fine-structure states of the Ni cations in the complex. The lowest electronic excitation energies of the dibenzotetraaza[14]annulene Ni(II) complex calculated at the time-dependent density functional theory (TDDFT) levels are in good agreement with values deduced from the experimental UV-vis spectrum. Calculations at the second-order algebraic-diagrammatic construction (ADC(2)) level on the dimer of the meso-substituted 3,3-dimethylindolenine dibenzotetraaza[14] annulene Ni(II) complex yielded Stokes shifts of 85-100 nm for the lowest excited singlet states. Calculations of the strength of the magnetically induced ring current for the free-base 3,3-dimethylindolenine-substituted dibenzotetraaza[14]annulene show that the annulene

  7. New Mn(II, Ni(II, Cd(II, Pb(II complexes with 2-methylbenzimidazole and other ligands. Synthesis, spectroscopic characterization, crystal structure, magnetic susceptibility and biological activity studies

    Directory of Open Access Journals (Sweden)

    Shayma A. Shaker

    2016-11-01

    Full Text Available Synthesis and characterization of Mn(II, Ni(II, Cd(II and Pb(II mixed ligand complexes of 2-methylbenzimidazole with other ligands have been reported. The structure of the ligands and their complexes was investigated using elemental analysis, IR, UV–Vis, (1H, 13C NMR spectroscopy, molar conductivity and magnetic susceptibility measurements. In all the studies of complexes, the 2-methylbenzimidazole behaves as a neutral monodentate ligand which is coordinated with the metal ions through the N atom. While benzotriazole behaves as a neutral bidentate ligand which is coordinated with the Ni(II ion through the two N atoms. Moreover, the N-acetylglycine behaves as a bidentate ligand which is coordinated with the Mn(II, Ni(II and Pb(II ions through the N atom and the terminal carboxyl oxygen atom. The magnetic and spectral data indicate the tetrahedral geometry for Mn(II complex, irregular tetrahedral geometry for Pb(II complex and octahedral geometry for Ni(II complex. The X-ray single crystal diffraction method was used to confirm a centrosymmetric dinuclear Cd(II complex as each two metal ions are linked by a pair of thiocyanate N = S bridge. Two 2-methylbenzimidazole N-atom donors and one terminal thiocyanate N atom complete a highly distorted square pyramid geometry around the Cd atom. Besides, different cell types were used to determine the inhibitory effect of Mn(II, Ni(II, Cd(II and Pb(II complexes on cell growth using MTT assay. Cd(II complex showed cytotoxic effect on various types of cancer cell lines with different EC50 values.

  8. EPA allocates emission allowances for phase II plants

    International Nuclear Information System (INIS)

    Burkhart, L.A.

    1993-01-01

    The Environmental Protection Agency (EPA) last month issued a final rule allocating acid rain emission allowances for use after 2000 by most United States power plants. The rule sets the stage for significant pollution reduction through the emission trading system established by the Clean Air Act Amendments of 1990. The rule complements EPA's comprehensive, final acid rain rule for SO 2 , which was published in the January 11, 1993, Federal Register. Under this rule, SO 2 reductions will occur in two phases: Phase I begins in 1995 and sets allowances for 110 of the nation's largest plants, mostly coal-fired generators in eastern and midwestern states. Phase II begins in 2000 and further reduces emissions for Phase I plants, while it sets additional restrictions for about 800 smaller plants. The March 5 rules list allowance allocations for Phase II, enabling Phase II utilities to choose the most effective compliance strategy. In a related matter, the Chicago Board of Trade was expected to hold EPA's first annual auction of acid rain allowances on March 29. The auction allowed new utilities - those not automatically allocated allowances under the Clean Air Act - to purchase allowances. The direct sale of allowances will begin no later than June 1, at a price of $1,500 an allowance (to be adjusted yearly for inflation), and will continue on a first-come, first-served basis until none are left

  9. Mechanistic studies of the inhibition of MutT dGTPase by the carcinogenic metal Ni(II).

    Science.gov (United States)

    Porter, D W; Nelson, V C; Fivash, M J; Kasprzak, K S

    1996-12-01

    Promutagenic 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxo-dG) levels are increased in DNA of animals exposed to carcinogenic metals, such as Ni(II). Besides being generated directly in genomic DNA, 8-oxo-dG may be incorporated there from 8-oxo-7,8-dihydro-2'-deoxyguanosine 5'-triphosphate (8-oxo-dGTP), a product of oxidative damage to the nucleotide pool. The Escherichia coli dGTPase MutT, and analogous dGTPases in rats and humans, have been suggested as a defense against such incorporation because they hydrolyze 8-oxo-dGTP to 8-oxo-7,8-dihydro-2'-deoxyguanosine 5'-monophosphate (8-oxo-dGMP). MutT and its mammalian counterparts are Mg(II)-dependent enzymes. Ni(II), in turn, is known to interact antagonistically with Mg(II) in biological systems. Thus, we hypothesized that Ni(II) might inhibit the activity of MutT. As an initial examination of this hypothesis, we conducted enzyme kinetic studies of MutT to determine the effect of Ni(II) on MutT activity and the mechanisms involved. As found, Ni(II) inhibited MutT in a concentration-dependent manner when either dGTP or 8-oxo-dGTP was the nucleotide substrate. Ni(II) was determined to be an uncompetitive inhibitor of MutT with respect to Mg(II) when dGTP was the substrate, with apparent Ki of 1.2 mM Ni(II), and a noncompetitive inhibitor with respect to Mg(II) when 8-oxo-dGTP was the substrate, with apparent Ki of 0.9 mM Ni(II). Hence, the two metal cations did not compete with each other for binding at the MutT active site. This makes it difficult to predict Ni(II) effects on 8-oxo-dGTPases of other species. However, based upon the amino acid sequences of human and rat MutT-like dGTPases, their capacity for Ni(II) binding should be greater than that of MutT. Whether this could lead to stronger inhibition of those enzymes by Ni(II), or not, remains to be investigated.

  10. Synthesis, Characterization, and Catalytic Activities of A Nickel(II) Monoamido-Tetradentate Complex: Evidence For NiIII-Oxo and NiIV-Oxo Species.

    Science.gov (United States)

    Bok, Kwon Hee; Lee, Myoung Mi; You, Ga Rim; Ahn, Hye Mi; Ryu, Ka Young; Kim, Sung-Jin; Kim, Youngmee; Kim, Cheal

    2017-03-02

    A new mononuclear nickel(II) complex, [Ni II (dpaq)Cl] (1), containing a tetradentate monoamido ligand, dpaq (dpaq=2-[bis(pyridin-2-ylmethyl)amino]-N-(quinolin-8-yl)acetamide), has been synthesized and characterized by IR spectroscopy, elemental analysis, and UV/Vis spectroscopy. The structure of the nickel complex has been determined by X-ray crystallography. This nonheme Ni II complex 1 catalyzed the epoxidation reaction of a wide range of olefins with meta-chloroperoxybenzoic acid (m-CPBA) under mild conditions. Olefin epoxidation using this catalytic system has been proposed to involve a new reactive Ni IV -oxo (4) species, based on the evidence from a PPAA (peroxyphenylacetic acid) probe, Hammett studies, H 2 18 O exchange experiments, and ESI mass spectroscopic analysis. Moreover, the nature of solvent significantly influenced partitioning between heterolytic and homolytic O-O bond cleavage of the Ni-acylperoxo intermediate (2). The O-O bond of 2 proceeded predominantly through heterolytic cleavage in a protic solvent, such as CH 3 OH. These results suggest that possibly a Ni IV -oxo species is a common reactive intermediate in protic solvents. The two active oxidants, namely Ni IV -oxo (3) and Ni III -oxo (4), which are responsible for stereospecific olefin epoxidation and radical-type oxidations, respectively, operate in aprotic solvents. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. Synthesis, characterization, equilibrium study and biological activity of Cu(II), Ni(II) and Co(II) complexes of polydentate Schiff base ligand

    Science.gov (United States)

    El-Sherif, Ahmed A.; Shehata, Mohamed R.; Shoukry, Mohamed M.; Barakat, Mohammad H.

    2012-10-01

    Schiff base ligand, 1,4-bis[(2-hydroxybenzaldehyde)propyl]piperazine (BHPP), and its Cu(II), Ni(II) and Co(II) metal complexes were synthesized and characterized by elemental analysis, magnetic susceptibility, molar conductance and spectral (IR and UV-vis) studies. The ground state of BHPP ligand was investigated using the BUILDER module of MOE. Metal complexes are formed in the 1:1 (M:L) ratio as found from the elemental analysis and found to have the general formula [ML]·nH2O, where M = Co(II), Ni(II) and Cu(II), L = BHPP. In all the studied complexes, the (BHPP) ligand behaves as a hexadentate divalent anion with coordination involving the two azomethine nitrogen's, the two nitrogen atoms of piperazine ring and the two deprotonated phenolic OH-groups. The magnetic and spectral data indicates octahedral geometry of metal(II) complexes. The ligand and their metal chelates have been screened for their antimicrobial activities using the disc diffusion method against the selected bacteria and fungi. They were found to be more active against Gram-positive than Gram-negative bacteria. Protonation constants of (BHPP) ligand and stability constants of its Cu2+, Co2+ and Ni2+ complexes were determined by potentiometric titration method in 50% DMSO-water solution at ionic strength of 0.1 M sodium nitrate. It has been observed that the protonated Schiff base ligand (BHPP) have four protonation constants. The divalent metal ions Cu2+, Ni2+ and Co2+ form 1:1 complexes.

  12. Ni(II, Pd(II and Pt(II complexes with ligand containing thiosemicarbazone and semicarbazone moiety: synthesis, characterization and biological investigation

    Directory of Open Access Journals (Sweden)

    SULEKH CHANDRA

    2008-07-01

    Full Text Available The synthesis of nickel(II, palladium(II and platinum(II complexes with thiosemicarbazone and semicarbazone of p-tolualdehyde are reported. All the new compounds were characterized by elemental analysis, molar conductance measurements, magnetic susceptibility measurements, mass, 1H-NMR, IR and electronic spectral studies. Based on the molar conductance measurements in DMSO, the complexes may be formulated as [Ni(L2Cl2] and [M(L2]Cl2 (where M = Pd(II and Pt(II due to their non-electrolytic and 1:2 electrolytic nature, respectively. The spectral data are consistent with an octahedral geometry around Ni(II and a square planar geometry for Pd(II and Pt(II, in which the ligands act as bidentate chelating agents, coordinated through the nitrogen and sulphur/oxygen atoms. The ligands and their metal complexes were screened in vitro against fungal species Alternaria alternata, Aspergillus niger and Fusarium odum, using the food poison technique.

  13. SYNTHESIS OF POLYEUGENYL OXYACETIC ACID AS A CARRIER TO SEPARATE HEAVY METAL ION Fe (III, Cr(III, Cu(II, Ni(II, Co(II, AND Pb(II THAT USING SOLVENT EXTRACTION METHOD

    Directory of Open Access Journals (Sweden)

    La Harimu

    2010-06-01

    Full Text Available Polyeugenyl oxyacetic acid has been synthesized from polyeugenol and chloroacetic acid and applied to separate metal Fe(III, Cr(III, Cu(II, Ni(II, Co(II, and Pb(II using solvent extraction method. pH effect, polyeugenyl oxyacetic acid ion carrier concentration, extraction time, and metal concentration optimized to gain optimum condition. The result of experiment indicated that polyeugenyl oxyacetic acid resulted the yellowed brown synthesis with melting point 125 °C and yield 68.9%. The Characterization of spectroscopy IR attributed by absorption to the area 1735,8 cm -1 as carbonyl extend vibration (C=O acid and 1H-NMR that was attributed by chemical shift at 4.6 ppm as carboxy proton (CH2-C=0. The metal separation optimum condition gained pH 3-6 for ion Fe(III, pH 5 for ion Cr(III, Ni(II, and Co(II and pH 6 for ion Cu(II, and Pb(II. Optimum carrier concentraction 5 mL, 10 mL, and 15 mL for ion Fe(III, and ion Cr(III, Ni(II, Co(II, and ion Cu(II, Pb(II respectively. Extraction time 2.5 h for ion Fe(III, 20 h for ion Cr(III, and 36 h for ion Cu(II, Pb(II, Ni(II, and Co(II. Metal concentration that would extracted correctly (0.75-5 x 10-4 M for ion Fe(III, (0.75-2.5 x 10-4 M for ion Cr(III, Ni(II, and Co(II and (0.75-1 x 10-4 M for ion Cu(II and Pb(II. The best polyeugenil oxyacetic acid response to separate ion Fe(III than other ions with selectivity order Fe(III> Cr(III> Cu(II> Pb(II> Ni(II> Co(II.   Keywords: polyeugenil oxyacetic acid, pH, extraction time, metal concentraction, solvent extraction

  14. Synthesis, Crystal Structure, and Magnetic Properties of a New Mixed Metal (Co(II, Ni(II Cubane

    Directory of Open Access Journals (Sweden)

    Ramadan Mohamed Elmehdawi

    2017-02-01

    Full Text Available The mixed Co(II/Ni(II complex, [Co2.67Ni1.33L4(CH3COO2][BPh4]2·0.75H2O where HL = 4-(salicylaldimineantipyrine, was isolated as an orange solid from the reaction of 4-(salicylaldimineantipyrine, with mixed cobalt(II acetate and nickel(II acetate in ethanol. The complex was characterized by Frustrated Total Internal Reflection (FTIR, UltraViolet Visible spectroscopy (UV-Vis, X-ray single crystal diffraction, and by elemental analysis. The complex is composed of two symmetry independent cationic units, A and B. The two units are essentially isostructural; nevertheless, small differences exist between them. The units contain four metal atoms, arranged at the corners of a distorted cubane-like core alternately with phenoxy oxygen of the Schiff base. The overall eight corners occupied by metal ions in the asymmetric unit are shared between cobalt and nickel in a 5.33:2.67 ratio. Each metal divalent cation binds three coordinated sites from the corresponding tridentate Schiff base ligand, the fourth one is bound by the acetate oxygen, the fifth and the sixth donor sites come from the phenolate oxygens of other Schiff base ligands. Intermolecular hydrogen bonds join the complexes to the water molecules present in the crystal packing. The magnetic characterization was carried out for this new complex and for its isostructural counterpart containing only cobalt ions. The magnetic measurements for the cobalt(II/nickel(II mixed compound indicate either antiferromagnetic interactions among the two cubanes or an anisotropic contribution, whereas a ferromagnetic interaction is observed within the cubane, for both the complexes, as expected by geometrical considerations. A comparison between the magnetic properties of the pure cobalt(II derivative and similar systems discussed in literature, is presented.

  15. Micellar effect on metal-ligand complexes of Co(II, Ni(II, Cu(II and Zn(II with citric acid

    Directory of Open Access Journals (Sweden)

    Nageswara Rao Gollapalli

    2009-12-01

    Full Text Available Chemical speciation of citric acid complexes of Co(II, Ni(II, Cu(II and Zn(II was investigated pH-metrically in 0.0-2.5% anionic, cationic and neutral micellar media. The primary alkalimetric data were pruned with SCPHD program. The existence of different binary species was established from modeling studies using the computer program MINIQUAD75. Alkalimetric titrations were carried out in different relative concentrations (M:L:X = 1:2:5, 1:3:5, 1:5:3 of metal (M to citric acid. The selection of best chemical models was based on statistical parameters and residual analysis. The species detected were MLH, ML2, ML2H and ML2H2. The trend in variation of stability constants with change in mole fraction of the medium is explained on the basis of electrostatic and non-electrostatic forces. Distributions of the species with pH at different compositions of micellar media are also presented.

  16. Anion effect on the control of morphology for NiC2O4·2H2O nanostructures as precursors for synthesis of Ni(OH)2 and NiO nanostructures and their application for removing heavy metal ions of cadmium(II) and lead(II).

    Science.gov (United States)

    Behnoudnia, Fatemeh; Dehghani, Hossein

    2014-03-07

    In this work, one-dimensional (1-D) and three-dimensional (3-D) nickel oxalate dihydrate nanostructures have been selectively prepared by a one-step and surfactant-free solvothermal approach. This preparation procedure can control the product morphology by varying the reaction temperature and anions such as nitrates, acetates, chlorides and sulfates. The morphology of nickel oxalate dihydrate changed from non-uniform sheets and ribbons to nanorods with higher temperatures while changing the initial anion converted nanorods to dandelion-like nanostructures. Field emission scanning electron microscopy (FESEM) shows that the sizes of the nickel oxalate dihydrate nanorods are about 3 μm in length and the dandelion-like nanostructures have an average diameter of around 10 μm. Furthermore, the adsorption of the heavy metal ions of cadmium(ii) and lead(ii) with nanostructured nickel compounds was investigated. The results indicate the NiO and Ni(OH)2 nanostructures can effectively adsorb cadmium(ii) and lead(ii) ions from aqueous solution.

  17. Application of Ni(II-assisted peptide bond hydrolysis to non-enzymatic affinity tag removal.

    Directory of Open Access Journals (Sweden)

    Edyta Kopera

    Full Text Available In this study, we demonstrate a non-enzymatic method for hydrolytic peptide bond cleavage, applied to the removal of an affinity tag from a recombinant fusion protein, SPI2-SRHWAP-His(6. This method is based on a highly specific Ni(II reaction with (S/TXHZ peptide sequences. It can be applied for the protein attached to an affinity column or to the unbound protein in solution. We studied the effect of pH, temperature and Ni(II concentration on the efficacy of cleavage and developed an analytical protocol, which provides active protein with a 90% yield and ∼100% purity. The method works well in the presence of non-ionic detergents, DTT and GuHCl, therefore providing a viable alternative for currently used techniques.

  18. Synthesis, spectroscopic and antimicrobial properties of Co(II), Ni (II ...

    African Journals Online (AJOL)

    The objective of this study is to investigate the antimicrobial activity of novel Schiff base metal complexes. The resistance of micro-organisms to classical antimicrobial compounds poses a challenge to effective management and treatment of some diseases. In line with this, copper (II), nickel (II) and cobalt (II) complexes of ...

  19. Synthesis, Spectroscopic and Antimicrobial properties of Co(II), Ni (II ...

    African Journals Online (AJOL)

    ADOWIE PERE

    ABSTRACT: The objective of this study is to investigate the antimicrobial activity of novel. Schiff base metal complexes. The resistance of micro-organisms to classical antimicrobial compounds poses a challenge to effective management and treatment of some diseases. In line with this, copper (II), nickel (II) and cobalt (II) ...

  20. Synthesis, spectroscopic characterization, molecular modeling and antimicrobial activities of Mn(II), Co(II), Ni(II), Cu(II) complexes containing the tetradentate aza Schiff base ligand

    Science.gov (United States)

    Chandra, Sulekh; Ruchi

    2013-02-01

    Mn(II), Co(II), Ni(II), and Cu(II) complexes with a tetradentate macrocyclic ligand [1.2.5.6tetraoxo-3,4,7,8tetraaza-(1,2,3,4,5,6,7,8)tetrabenzene(L)] were synthesized and characterized by elemental analysis, molar conductance measurements, mass, nmr, i.r., electronic and e.p.r. spectral studies. All the complexes are non electrolytes in nature and may be formulated as [M(L)X2] [where, M = Mn(II), Co(II), Ni(II), Cu(II) and X = Cl-, CH3COO-]. On the basis of i.r., electronic and e.p.r. spectral studies a distorted octahedral geometry has been assigned for all complexes. The antimicrobial activities and LD50 values of the ligand and its complexes, as growth inhibiting agents, have been screened in vitro against two different species of bacteria and plant pathogenic fungi.

  1. Kinetic and thermodynamic studies of the Co(II) and Ni(II) ions removal from aqueous solutions by Ca-Mg phosphates.

    Science.gov (United States)

    Ivanets, A I; Srivastava, V; Kitikova, N V; Shashkova, I L; Sillanpää, M

    2017-03-01

    The aim of this work was to study the sorption kinetics and thermodynamics of Co(II) and Ni(II) from aqueous solutions by sorbents on the basis of hydrogen (PD-1) and tertiary (PD-2) Ca-Mg phosphates depending on the solution temperature and sorbents chemical composition. Kinetic studies of adsorption of Co(II) and Ni(II) ions onto samples of phosphate sorbents were performed in batch experiment at the temperatures 288, 303, 318 and 333 K. The sorbent dose was fixed at 10 g L -1 , initial pH value 2.6, and contact time varied from 5 to 600 min. The kinetics of Co(II) and Ni(II) adsorption were analyzed by using pseudo-first order, pseudo-second order and intraparticle diffusion models. Thermodynamic parameters (ΔG°, ΔH° and ΔS°) for the sorption of Co(II) and Ni(II) were determined using the Gibbs-Helmholtz equation. The calculated kinetic parameters and corresponding correlation coefficients revealed that Co(II) and Ni(II) uptake process followed the pseudo-second order rate expression. Thermodynamic studies confirmed the spontaneous and endothermic nature of removal process which indicate that sorption of Co(II) and Ni(II) ions onto both phosphate sorbents is favoured at higher temperatures and has the chemisorptive mechanism. The data thus obtained would be useful for practical application of the low cost and highly effective Ca-Mg phosphate sorbents. Copyright © 2016 Elsevier Ltd. All rights reserved.

  2. Synthesis and characterization of a new nonanuclear Ni(II) cluster from a pyridyl-alcohol ligand.

    Science.gov (United States)

    Massard, Alexandre; Rogez, Guillaume; Braunstein, Pierre

    2014-01-07

    The reaction of one equivalent of 2-methyl-1-(pyridin-2-yl)propan-2-ol (HL) with two equivalents of [Ni(OAc)2·4H2O] in methanol afforded the nonanuclear coordination cluster [Ni9(HL-κ(2)N,O)4(OAc-κ(2)O)2(μ2-OAc-κ(1)O)2(μ2-OAc-κ(2)O,O')4(μ3-OAc-κ(2)O;κ(2)O,O')2(μ3-OMe)8] (1). All nickel ions are hexacoordinated and show a slightly distorted octahedral coordination geometry. This unusual centrosymmetric coordination cluster can be described as constituted by two cubane moieties connected by a linker comprising a nickel atom, situated on the inversion centre, four bridging acetates and two triply-bridging acetates. Each cubane contains four Ni(II) centres and four triply-bridging methoxide anions, two of the Ni(II) centres are N,O-chelated by the ligand HL, another Ni(II) is chelated by an acetate ligand and the fourth Ni(II) centre is connected to the exo-cubane Ni(II) through three acetate ligands which each have a different bonding mode: μ2-κ(2)O,O', μ2-κ(1)O, and μ3-κ(1)O;κ(2)O,O'. The magnetic and catalytic properties for ethylene oligomerization of the unusual complex have been investigated.

  3. FeII/MgII Emission Line Ratio in High Redshift Quasars

    DEFF Research Database (Denmark)

    Dietrich, M.; Hamann, F.; Appenzeller, I.

    2003-01-01

    We present results of the analysis of near infrared spectroscopic observations of 6 high-redshift quasars (z > 4), emphasizing the measurement of the ultraviolet FeII/MgII emission line strength in order to estimate the beginning of intense star formation in the early universe. To investigate the.......3, Omega_Lambda = 0.7). This epoch corresponds well to the re-ionization era of the universe....... the evolution of the FeII/MgII ratio over a wider range in cosmic time, we measured this ratio for composite quasar spectra which cover a redshift range of 0 4 quasars must have started already at an epoch corresponding to z_f = 6 to 9, when the age of the universe was ~0.5 Gyr (H_o = 72 km/s/Mpc, Omega_M = 0...

  4. Synthesis, spectral analysis, stability constants, antioxidant and biological activities of Co (II), Ni (II) and Cu (II) mixed ligand complexes of nicotinamide, theophylline and thiocyanate

    Science.gov (United States)

    Altun, Özlen; Şuözer, Mehtap

    2017-12-01

    In the present study, transition metal complexes or coordination entities with metal precursors such as Co (II), Ni (II) and Cu (II) of mixed ligands namely, nicotinamide (NA), theophylline (TP) and KSCN in water were synthesized under refluxing conditions. The optimization of the reactions to obtain the composition of complexes was performed. The structural elucidation of the complexes was undertaken by using physico-chemical and spectroscopic methods (UV/Vis, FT-IR, Mass and XRD) and thermal analysis. The spectral measurements of mixed ligands with the Co (II), Ni (II) and Cu (II) complexes are compared with each other in determining which atoms of the ligand are coordinated to the metal ion. Based on spectral and magnetic moment measurements, all the coordination entities were identified as in distorted octahedral structure and have the form [M(NA)2 (TP)2(SCN)2]·xH2O. In addition, K (stability constant) and ΔG (Gibbs free energy) values were calculated by using the Babko and Stanley & Turner's methods. Antioxidant, antibacterial and antifungal activities of the complexes were studied.

  5. 1-Naphthylazo derivatives of some 1,3-dicarbonyl compounds and their Cu(II, Ni(II and Zn(II complexes

    Directory of Open Access Journals (Sweden)

    K. KRISHNANKUTTY

    2009-11-01

    Full Text Available The coupling of diazotized 1-aminonaphthalene with 1,3-dicarbonyl compounds (acetylacetone, methylacetoacetate and acetoacetanilide yielded a new series of bidentate ligand systems (HL. Analytical, IR, 1H-NMR and mass spectral data indicate that the compounds exist in the intramolecularly hydrogen bonded keto-hydrazone form. With Ni(II, Cu(II and Zn(II, these potential monobasic bidentate ligands formed [ML2] type complexes. The IR, 1H-NMR and mass spectral data of the complexes are consistent with the replacement of the chelated hydrazone proton of the ligand by a metal ion, thus leading to a stable six-membered chelate ring involving the hydrazone nitrogen and the hydrogen bonded carbonyl oxygen. The Ni(II and Zn(II chelates are diamagnetic, while the Cu(II complexes are paramagnetic. In the metal complexes of the naphthylazo derivatives of acetylacetone and methylacetoacetate, the acetyl carbonyl is involved in coordination, whereas in the chelates of the naphthylazo derivative of acetoacetanilide, the anilide carbonyl is bonded with the metal ion.

  6. Mg II h and k emission from luminous M stars

    Science.gov (United States)

    Bernat, A. P.; Lambert, D. L.

    1978-01-01

    Mg II h and k emission lines of the M2 giant beta Peg and the M5 supergiant alpha Her were detected in Copernicus observations. In the alpha Her profiles, similar to alpha Ori and alpha Sco profiles, the k line is asymmetric and the h line is symmetric. The possibility that the k line asymmetry is produced by overlying absorption is discussed. In beta Peg, both h and k lines are asymmetric, and line formation in an expanding chromosphere is indicated. The observations are in accord with one formulation of the Wilson-Bappu relation but deviate from another form of the Wilson-Bappu relation.

  7. Comparison between Ag (I and Ni (II Removal from Synthetic Nuclear Power Plant Coolant Water by Iron Oxide Nanoparticles

    Directory of Open Access Journals (Sweden)

    Mohammad Hossein Salmani

    2013-07-01

    Full Text Available The impact of effective parameters such as iron oxide nanoparticles dosage, contact time and solution pH was optimized for removal of Ag(I and Ni(II in the nuclear cooling system and the best conditions were compared. Nearly complete removal (97% of Ni(II and Ag(I were obtained at adsorbent dosage of 40 and 20 g/L, respectively. Experiments showed that 4 hours was a good choice as optimum contact time for two ions removal. The effective parameter was pH, so that maximum removal efficiency was obtained for Ag(I in acidic pH=3 and for Ni(II in basic pH=10. It seems that removal of Ag(I was controlled by adsorption-reduction mechanism, but Ni(II could place only adsorption. Langmuir and Freundlich model was more suitable for nickel and silver removal by this adsorbent, respectively. Ag(I and Ni(II removal efficiency trend by this adsorbent is similar at periods but different in the concentrations, pHs and equilibrium model. The obtained results were very promising, as both Ag(I and Ni(II were effectively removed from synthetic wastewater and there was a possibility to remove Ag(I very fast. Hence, the idea of using nanoparticles for application of metal ions removal from wastewaters seems to be very efficient and quite promising.

  8. Interannual variation in methane emissions from tropical wetlands triggered by repeated El Niño Southern Oscillation

    Science.gov (United States)

    Zhu, Qiuan; Peng, Changhui; Ciais, Philippe; Jiang, Hong; Liu, Jinxun; Bousquet, Philippe; Li, Shiqin; Chang, Jie; Fang, Xiuqin; Zhou, Xiaolu; Chen, Huai; Liu, Shirong; Lin, Guanghui; Gong, Peng; Wang, Meng; Wang, Han; Xiang, Wenhua; Chen, Jing

    2017-01-01

    Methane (CH4) emissions from tropical wetlands contribute 60%–80% of global natural wetland CH4 emissions. Decreased wetland CH4 emissions can act as a negative feedback mechanism for future climate warming and vice versa. The impact of the El Niño–Southern Oscillation (ENSO) on CH4 emissions from wetlands remains poorly quantified at both regional and global scales, and El Niño events are expected to become more severe based on climate models’ projections. We use a process-based model of global wetland CH4 emissions to investigate the impacts of the ENSO on CH4 emissions in tropical wetlands for the period from 1950 to 2012. The results show that CH4 emissions from tropical wetlands respond strongly to repeated ENSO events, with negative anomalies occurring during El Niño periods and with positive anomalies occurring during La Niña periods. An approximately 8-month time lag was detected between tropical wetland CH4 emissions and ENSO events, which was caused by the combined time lag effects of ENSO events on precipitation and temperature over tropical wetlands. The ENSO can explain 49% of interannual variations for tropical wetland CH4 emissions. Furthermore, relative to neutral years, changes in temperature have much stronger effects on tropical wetland CH4 emissions than the changes in precipitation during ENSO periods. The occurrence of several El Niño events contributed to a lower decadal mean growth rate in atmospheric CH4 concentrations throughout the 1980s and 1990s and to stable atmospheric CH4 concentrations from 1999 to 2006, resulting in negative feedback to global warming.

  9. Synthesis, crystal structure and photoluminescence study of green light emitting bis(1[(4-butylphenylimino]methyl naphthalen-2-ol Ni(II complex

    Directory of Open Access Journals (Sweden)

    M. Srinivas

    2016-09-01

    Full Text Available Synthetically feasible and cost effective Ni(II complex phosphor (4 as green organic light emitting diode (OLED was prepared by using Schiff base 1-[(4-butylphenylimino]methyl naphthalen-2-ol (3. The single crystals of Ni(II complex were grown from chloroform and hexane (1:1 v/v solution. The green crystals of the complex were characterized by using single crystal XRD studies and were evaluated for their photophysical properties. From the Diffused Reflectance Spectrum of the complex, the measured band gap energy was found to be 1.83 eV and the PL spectrum of the complex showed emission peak at 519 nm. The excitation peaks at 519 nm were appeared at 394 nm and 465 nm. The Commission Internationale De L'Eclairage (CIE chromaticity diagram indicated that, the complex exhibit green color. Hence, Ni(II complex (4 could be a promising green OLED for developing strong electroluminescent materials for flat panel display applications.

  10. Synthesis, characterization and in vitro anticancer activity of 18-membered octaazamacrocyclic complexes of Co(II), Ni(II), Cd(II) and Sn(II)

    Science.gov (United States)

    Kareem, Abdul; Zafar, Hina; Sherwani, Asif; Mohammad, Owais; Khan, Tahir Ali

    2014-10-01

    An effective series of 18 membered octaazamacrocyclic complexes of the type [MLX2], where X = Cl or NO3 have been synthesized by template condensation reaction of oxalyl dihydrazide with dibenzoylmethane and metal salt in 2:2:1 molar ratio. The formation of macrocyclic framework, stereochemistry and their overall geometry have been characterized by various physico-chemical studies viz., elemental analysis, electron spray ionization-mass spectrometry (ESI-MS), I.R, UV-Vis, 1H NMR, 13C NMR spectroscopy, X-ray diffraction (XRD) and TGA/DTA studies. These studies suggest formation of octahedral macrocyclic complexes of Co(II), Ni(II), Cd(II) and Sn(II). The molar conductance values suggest nonelectrolytic nature for all the complexes. Thermogravimatric analysis shows that all the complexes are stable up to 600 °C. All these complexes have been tested against different human cancer cell lines i.e. human hepatocellular carcinoma (Hep3B), human cervical carcinoma (HeLa), human breast adenocarcinoma (MCF7) and normal cells (PBMC). The newly synthesized 18-membered octaazamacrocyclic complexes during in vitro anticancer evaluation, displayed moderate to good cytotoxicity on liver (Hep3B), cervical (HeLa) and breast (MCF7) cancer cell lines, respectively. The most effective anticancer cadmium complex (C34H28N10CdO10) was found to be active with IC50 values, 2.44 ± 1.500, 3.55 ± 1.600 and 4.82 ± 1.400 in micro-molar on liver, cervical and breast cancer cell lines, respectively.

  11. Adsorption of Ni(II, Cu(II and Fe(III from Aqueous Solutions Using Activated Carbon

    Directory of Open Access Journals (Sweden)

    A. Edwin Vasu

    2008-01-01

    Full Text Available An activated carbon was tested for its ability to remove transition metal ions from aqueous solutions. Physical, Chemical and liquid-phase adsorption characterizations of the carbon were done following standard procedures. Studies on the removal of Ni(II, Cu(II and Fe(III ions were attempted by varying adsorbate dose, pH of the metal ion solution and time in batch mode. The equilibrium adsorption data were fitted with Freundlich, Langmuir and Redlich-Peterson isotherms and the isotherm constants were evaluated. Time variation studies indicate that adsorptions follow pseudo-second order kinetics. pH was found to have a significant role to play in the adsorption. The processes were endothermic and the thermodynamic parameters were evaluated. Desorption studies indicate that ion-exchange mechanism is operating.

  12. Galvanic displacement synthesis of Al/Ni core–shell pigments and their low infrared emissivity application

    Energy Technology Data Exchange (ETDEWEB)

    Yuan, Le, E-mail: yuanle.cn@gmail.com [Center for Advanced Materials and Energy, Xihua University, Chengdu, 610039 (China); National Engineering Research Center of Electromagnetic Radiation Control Materials, UESTC, Chengdu, 610054 (China); Hu, Juan [Center for Advanced Materials and Energy, Xihua University, Chengdu, 610039 (China); Weng, Xiaolong [National Engineering Research Center of Electromagnetic Radiation Control Materials, UESTC, Chengdu, 610054 (China); Zhang, Qingyong [Center for Advanced Materials and Energy, Xihua University, Chengdu, 610039 (China); Deng, Longjiang [National Engineering Research Center of Electromagnetic Radiation Control Materials, UESTC, Chengdu, 610054 (China)

    2016-06-15

    We have successfully developed a magnetic Al/Ni core–shell pigment via a galvanic displacement reaction to obtain low infrared emissivity pigment with low lightness and visible light reflectance. Al/Ni core–shell particles were prepared via a simple one-step synthetic method where Ni was deposited onto the Al surface at the expense of Al atoms. The influence of pH and the amount of NH{sub 4}F complexing agent on phase structure, surface morphology, optical and magnetic properties were studied systematically. The neutral condition and high concentration of NH{sub 4}F forms smooth, flat, uniform and dense Ni shell on the surface of flake Al particles, which can significantly reduce the lightness and visible light reflectance but slightly increase the infrared emissivity. When the core–shell pigments are prepared in neutral pH solution at NH{sub 4}F = 11.2 g/L, the lightness (L{sup *}) and visual light reflectivity can be reduced by 12.6 and 0.46, respectively versus uncoated flake Al pigments, but the infrared emissivity is only increased by 0.02. The color changes from brilliant silver to gray black and the saturation magnetization value is 6.59 emu/g. Therefore, these Al/Ni magnetic composite pigments can be used as a novel low infrared emissivity pigment to improve the multispectral stealth performance of low-E coatings in the visual, IR and Radar wavebands. - Highlights: • Prepared magnetic Al/Ni core–shell pigment with low lightness and low emissivity. • Used one-pot galvanic displacement reaction to form smooth and dense Ni shell. • Show enhanced stealth performance in the visual, IR and Radar wavebands. • The lightness and visible light reflectance was decreased by 12.6 and 0.46. • But the infrared emissivity was only increases by 0.02.

  13. Application of Carrier Element-Free Co-precipitation Method for Ni(II), Cu(II) and Zn(II) Ions Determination in Water Samples Using Chrysin

    International Nuclear Information System (INIS)

    Layth Imad Abd Ali; Wan Aini Wan Ibrahim; Azli Sulaiman; Mohd Marsin Sanagi

    2015-01-01

    A co-precipitation method was developed to separate and pre-concentrate Ni(II), Cu(II) and Zn(II) ions using an organic co precipitant, chrysin without adding any carrier element termed as carrier element-free co-precipitation (CEFC). Analytes were determined using flame atomic absorption spectrometry (FAAS). The influence of analytical conditions, such as pH of the solution, quantity of co-precipitant, standing time, centrifugation rate and time, sample volume, and interference of concomitant ions were investigated over the recovery yields of the trace metals. The limit of detection, the limit of quantification and linearity range obtained from the FAAS measurements were found to be in the range of 0.64 to 0.86 μg L -1 , 2.13 to 2.86 μg L -1 and 0.9972 to 0.9989 for Ni(II), Cu(III) and Zn(II) ions, respectively. The precision of the method, evaluated as the relative standard deviation (RSD) obtained after analyzing a series of 10 replicates, was between 2.6 % to 3.9 % for the trace metal ions. The proposed procedure was applied and validated by analyzing river water reference material for trace metals (SLRS-5) and spiking trace metal ions in some water samples. The recoveries of the analyte metal ions were between 94.7-101.2 %. (author)

  14. Spectral characteristic investigation on complex of Ni (II) with captopril and its analytical application

    Science.gov (United States)

    Wei, Xiaoling; Du, Liangwei; Li, Dongmei; Gong, Qi; Wang, Lisheng; Lin, Yu

    In this paper, Ni (II) reacting with captopril (CPT) can form complex in alkaline solution and the formed complex has a characteristic absorption peak at 340 nm. The absorbance of the Ni-CPT complex increases linearly with the increased concentration of captopril. The study also shows that ammonia has an obvious sensitizing effect on the absorbance. Based on the study, a new method for the determination of captopril is established. Experimental results show that the linear range of this method under optimum condition is 1.0-60 mg/L with correlation coefficient, detection limit and precision of 0.9999, 0.31 mg/L and 0.87%, respectively. The method used to determine captopril in commercial captopril tablets has a satisfactory result with the recoveries in the range of 99.0-103.6% and the relative standard deviation (RSD) in the range of 0.8-3.7%. We preliminarily study the reaction mechanism and demonstrate that the complex ratio of Ni (II) with captopril is 1:2 and the formation constant is 6.3 × 109.

  15. Synthesis of Highly Branched Polyolefins Using Phenyl Substituted α-Diimine Ni(II Catalysts

    Directory of Open Access Journals (Sweden)

    Fuzhou Wang

    2016-04-01

    Full Text Available A series of α-diimine Ni(II complexes containing bulky phenyl groups, [ArN = C(NaphthC = NAr]NiBr2 (Naphth: 1,8-naphthdiyl, Ar = 2,6-Me2-4-PhC6H2 (C1; Ar = 2,4-Me2-6-PhC6H2 (C2; Ar = 2-Me-4,6-Ph2C6H2 (C3; Ar = 4-Me-2,6-Ph2C6H2 (C4; Ar = 4-Me-2-PhC6H3 (C5; Ar = 2,4,6-Ph3C6H2 (C6, were synthesized and characterized. Upon activation with either diethylaluminum chloride (Et2AlCl or modified methylaluminoxane (MMAO, all Ni(II complexes showed high activities in ethylene polymerization and produced highly branched amorphous polyethylene (up to 145 branches/1000 carbons. Interestingly, the sec-butyl branches were observed in polyethylene depending on polymerization temperature. Polymerization of 1-alkene (1-hexene, 1-octene, 1-decene and 1-hexadecene with C1-MMAO at room temperature resulted in branched polyolefins with narrow Mw/Mn values (ca. 1.2, which suggested a living polymerization. The polymerization results indicated the possibility of precise microstructure control, depending on the polymerization temperature and types of monomers.

  16. Spectroscopic and thermal degradation behavior of Cr(III), Mn(II), Fe(III), Co(II), Ni(II), Cu(II) and Zn(II) complexes with thiopental sodium anesthesia drug

    Science.gov (United States)

    Refat, Moamen S.

    2013-04-01

    A new series of Cr(III), Mn(II), Fe(III), Co(II), Ni(II), Cu(II) and Zn(II) complexes have been synthesized with thiopental sodium anesthesia drug. The elemental analyses of the complexes are confined to stoichiometry of the formulas [M(TPL)3]ṡnH2O (M = Cr(III) or Fe(III); n = 6 or 5), [M(TPL)2(H2O)2]ṡnH2O (M = Mn(II), Co(II) or Ni(II); n = 0 or 4), and [M(TPL)2] (M = Cu(II) or Zn(II); n = 2 or 0) respectively, where TPL is thiopental chelating agent. Structures have been discussed and suggested upon elemental analyses, infrared, Raman, electronic, electron spin resonance, 1H NMR spectral data and magnetic studies. The X-ray powder diffraction (XRD) was performed of metal complexes. The XRD patterns indicate crystalline nature for the complexes. The measured low molar conductance values in dimethylsulfoxide indicate that the complexes are non-electrolyte nature. Spectroscopic discussion refer that coordination take place through three types: Cdbnd N (pyrimidine moiety) nitrogen and C2sbnd S (2-thiolate group) for Cr(III), Mn(II) and Fe(III), C6dbnd O (amido group) oxygen and C2sbnd S (2-thiolate group) for Co(II) and Ni(II), and Cu(II) and Zn(II) ions coordinated via Cdbnd N (pyrimidine moiety) nitrogen, C2dbnd S (2-thiolate group) and C6dbnd O (amido group) oxygen, respectively. The thermal behavior (TG/DTG/DTA) of the complexes was studied and kinetic parameters were determined by Horowitz-Metzger and Coats-Redfern methods. The thiopental and its complexes have been screened for their antimicrobial (G+ and G-) bacteria (Escherichia coli, Staphylococcus aureus, Bacillus subtilis and Pseudomonas aeruginosa) and fungi (Aspergillus flavus and Candida albicans) activities by minimum inhibitory concentration (MIC) method.

  17. Kinetic study on adsorption of Cr(VI), Ni(II), Cd(II) and Pb(II) ions from aqueous solutions using activated carbon prepared from Cucumis melo peel

    Science.gov (United States)

    Manjuladevi, M.; Anitha, R.; Manonmani, S.

    2018-03-01

    The adsorption of Cr(VI), Ni(II), Cd(II) and Pb(II), ions from aqueous solutions by Cucumis melo peel-activated carbon was investigated under laboratory conditions to assess its potential in removing metal ions. The adsorption behavior of metal ions onto CMAC was analyzed with Elovich, intra-particle diffusion rate equations and pseudo-first-order model. The rate constant of Elovich and intra-particle diffusion on CMAC increased in the sequence of Cr(VI) > Ni(II) > Cd(II) > Pb(II). According to the regression coefficients, it was observed that the kinetic adsorption data can fit better by the pseudo-first-order model compared to the second-order Lagergren's model with R 2 > 0.957. The maximum adsorption of metal ions onto the CMAC was found to be 97.95% for Chromium(VI), 98.78% for Ni(II), 98.55% for Pb(II) and 97.96% for Cd(II) at CMAC dose of 250 mg. The adsorption capacities followed the sequence Ni(II) ≈ Pb(II) > Cr(VI) ≈ Cd(II) and Ni(II) > Pb(II) > Cd(II) > Cr(VI). The optimum adsorption conditions selected were adsorbent dosage of 250 mg, pH of 3.0 for Cr(VI) and 6.0 for Ni(II), Cd(II) and Pb(II), adsorption concentration of 250 mg/L and contact time of 180.

  18. Synthesis, characterization and anti-microbial activity of a novel macrocyclic ligand derived from the reaction of 2,6-pyridinedicarboxylic acid with homopiperazine and its Co(II), Ni(II), Cu(II), and Zn(II) complexes

    Science.gov (United States)

    Soleimani, Esmaiel

    2011-05-01

    The preparation of a novel macrocyclic ligand ( 1), N,N'-diethylhomopiperazinyl,2,6-pyridinedicarboxylate and its Co(II), Ni(II), Cu(II), and Zn(II) complexes are described. The ligand was prepared in EtOH from the reaction of dipotassium salt of 2,6-pyridinedicarboxylic acid with 1,2-dibromoethane in the presence of homopiperazine. Reaction of macrocyclic ligand ( 1) in EtOH with CoCl 2.6H 2O, NiCl 2.6H 2O, CuCl 2.2H 2O, and ZnCl 2·2H 2O yielded the complexes with the general formula [M(L)Cl 2] {where M = Co(II) ( 2), Ni(II) ( 3), Cu(II) ( 4), Zn ( 5), respectively}. The analysis of IR, 1H and 13C NMR spectral data of macrocyclic ligand ( 1) and its Zn(II) complex ( 5) together with their molar conductivity values, and the magnetic moments of the complexes suggest that the macrocyclic ligand ( 1) is bonded to metal(II) ions through two oxygen atoms of ester moiety and the two nitrogen atoms of homopiperazine ring. The electronic spectral data of these complexes in DMSO are in good agreement with the octahedral coordination of M(II) ions. The ligand field parameters for these complexes, i.e. splitting energy and Racah parameter were calculated to be 14,945 and 673 cm -1 for the Co(II) ( 2), 16,260 and 774 cm -1 for the Ni(II) ( 3) complexes respectively. The spliting energy of 17,262 cm -1 was obtained for the Cu(II) complex ( 4).

  19. Preparation and Spectral Properties of Mixed-Ligand Complexes of VO(IV, Ni(II, Zn(II, Pd(II, Cd(II and Pb(II with Dimethylglyoxime and N-acetylglycine

    Directory of Open Access Journals (Sweden)

    Shayma A. Shaker

    2010-01-01

    Full Text Available A number of mixed-ligand complexes of the general formula [M(D(G] where D=dimethylglyoximato monoanion, G=N-acetylglycinato and M=VO(IV, Ni(II, Zn(II, Pd(II, Cd(II and Pb(II were prepared. Each complex was characterized by elemental analysis, determination of metal, infrared spectra, electronic spectra, (1H and 13C NMR spectra, conductivity and magnetic moments. All these complexes were not soluble in some of the organic solvent but highly soluble in dimethylformamide. The conductivity data showed the non-electrolytic nature of the complexes. The electronic spectra exhibited absorption bands in the visible region caused by the d-d electronic transition such as VO(IV, Ni(II and Pd(II. The IR and (1H, 13C NMR spectra which have indicate that the dimethylglyoxime was coordinated with the metal ions through the N and O atoms of the oxime group and N-acetylglycine was coordinated with metal ions through the N atom and terminal carboxyl oxygen atom.

  20. Removal of Cu(II) and Ni(II) ions from an aqueous solution using α-Fe₂O₃nanoparticle-coated volcanic rocks.

    Science.gov (United States)

    Zhu, Xianfang; Song, Tiehong; Lv, Zhuo; Ji, Guodong

    2015-01-01

    An adsorbent, volcanic rocks coated with α-Fe₂O₃nanoparticles, was prepared and utilized for the removal of Cu(II) and Ni(II) ions from an aqueous solution. Characterization of the coated volcanic rocks indicated that the α-Fe₂O₃nanoparticles were successfully and homogeneously distributed on the volcanic rocks, including penetration into rock pores. Batch experiments were conducted to investigate adsorption performance. The adsorption behavior of both ions was found to best fit a pseudo second-order model and Langmuir isotherm. The maximum adsorption capacities of Cu(II) and Ni(II) ions were 58.14 mg g⁻¹ and 56.50 mg g⁻¹ at 293 K, respectively, and increased with rising temperature. The loaded α-Fe₂O₃nanoparticles onto volcanic rock significantly increased removal of Cu(II) and Ni(II) ions. The adsorption process was combined control of film diffusion and intra-particle diffusion. Adsorption thermodynamics indicated the adsorption process was spontaneous and occurred mainly through chemisorption. The results confirmed that the volcanic rocks coated with α-Fe₂O₃nanoparticles acted as a high-efficiency and low-cost absorbent, and effectively removed Cu(II) and Ni(II) from wastewater.

  1. Solid phase extraction-inductively coupled plasma spectrometry for adsorption of Co(II) and Ni(II) from radioactive wastewaters by natural and modified zeolites

    International Nuclear Information System (INIS)

    Akbar Malekpour; Mohammad Edrisi; Shamsollah Shirzadi; Saeed Hajialigol

    2011-01-01

    Natural and modified clinoptilolite as low-cost adsorbents have been used for adsorption of Co(II) and Ni(II) from nuclear wastewaters both in batch and continuous experiments. Zeolite X was also synthesized and its ability towards the selected cations was examined. Kinetic and thermodynamic behaviors for the process were investigated and adsorption equilibrium was interpreted in term of Langmuir and Freundlich equations. The effect of various parameters including the initial concentration, temperature, ionic strength and pH of solution were examined to achieve the optimized conditions. The clinoptilolite was shown good sorption potential for Co(II) and Ni(II) ions at pH values 4-6. Based on desorption studies, nearly 74 and 85% of adsorbed Co(II) and Ni(II) were removed from clinoptilolite by HCl. The Na + and NH 4 + forms of clinoptilolite were the best modified forms for the removal of investigated cations. It is concluded that the selectivity of clinoptilolite is higher for Co(II) than Ni(II). The synthesized zeolite showed more ability to remove cobalt and nickel ions from aqueous solution than the natural clinoptilolite. The microwave irradiation was found to be more rapid and effective for ion exchange compared to conventional ion exchange process. (author)

  2. Glutamate Ligation in the Ni(II)- and Co(II)-Responsive Escherichia coli Transcriptional Regulator, RcnR

    Energy Technology Data Exchange (ETDEWEB)

    Carr, Carolyn E. [Department of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, United States; Musiani, Francesco [Laboratory; Huang, Hsin-Ting [Department of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, United States; Chivers, Peter T. [Departments of Biosciences and Chemistry, Durham University, Durham DH1 3LE, United Kingdom; Ciurli, Stefano [Laboratory; Maroney, Michael J. [Department of Chemistry, University of Massachusetts, Amherst, Massachusetts 01003, United States

    2017-05-18

    Escherichia coli RcnR (resistance to cobalt and nickel regulator, EcRcnR) is a metal-responsive repressor of the genes encoding the Ni(II) and Co(II) exporter proteins RcnAB by binding to PRcnAB. The DNA binding affinity is weakened when the cognate ions Ni(II) and Co(II) bind to EcRcnR in a six-coordinate site that features a (N/O)5S ligand donor-atom set in distinct sites: while both metal ions are bound by the N terminus, Cys35, and His64, Co(II) is additionally bound by His3. On the other hand, the noncognate Zn(II) and Cu(I) ions feature a lower coordination number, have a solvent-accessible binding site, and coordinate protein ligands that do not include the N-terminal amine. A molecular model of apo-EcRcnR suggested potential roles for Glu34 and Glu63 in binding Ni(II) and Co(II) to EcRcnR. The roles of Glu34 and Glu63 in metal binding, metal selectivity, and function were therefore investigated using a structure/function approach. X-ray absorption spectroscopy was used to assess the structural changes in the Ni(II), Co(II), and Zn(II) binding sites of Glu → Ala and Glu → Cys variants at both positions. The effect of these structural alterations on the regulation of PrcnA by EcRcnR in response to metal binding was explored using LacZ reporter assays. These combined studies indicate that while Glu63 is a ligand for both metal ions, Glu34 is a ligand for Co(II) but possibly not for Ni(II). The Glu34 variants affect the structure of the cognate metal sites, but they have no effect on the transcriptional response. In contrast, the Glu63 variants affect both the structure and transcriptional response, although they do not completely abolish the function of EcRcnR. The structure of the Zn(II) site is not significantly perturbed by any of the glutamic acid variations. The spectroscopic and functional data obtained on the mutants were used to calculate models of the metal-site structures of EcRcnR bound to Ni(II), Co(II), and Zn(II). The results are interpreted

  3. Synthesis, investigation and spectroscopic characterization of piroxicam ternary complexes of Fe(II), Fe(III), Co(II), Ni(II), Cu(II) and Zn(II) with glycine and DL-phenylalanine

    Science.gov (United States)

    Mohamed, Gehad G.; El-Gamel, Nadia E. A.

    2004-11-01

    The ternary piroxicam (Pir; 4-hydroxy-2-methyl- N-(2-pyridyl)-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide) complexes of Fe(II), Fe(III), Co(II), Ni(II), Cu(II) and Zn(II) with various amino acids (AA) such as glycine (Gly) or DL-phenylalanine (PhA) were prepared and characterized by elemental analyses, molar conductance, IR, UV-Vis, magnetic moment, diffuse reflectance and X-ray powder diffraction. The UV-Vis spectra of Pir and the effect of metal chelation on the different interligand transitions are discussed in detailed manner. IR and UV-Vis spectra confirm that Pir behaves as a neutral bidentate ligand coordinated to the metal ions via the pyridine- N and carbonyl group of the amide moiety. Gly molecule acted as a uninegatively monodentate ligand and coordinate to the metal ions through its carboxylic group, in addition PhA acted as a uninegatively bidentate ligand and coordinate to the metal ions through its carboxylic and amino groups. All the chelates have octahedral geometrical structures while Cu(II)- and Zn(II)-ternary chelates with PhA have square planar geometrical structures. The molar conductance data reveal that most of these chelates are non electrolytes, while Fe(III)-Pir-Gly, Co(II)-, Ni(II)-, Cu(II)- and Zn(II)-Pir-PhA cheletes were 1:1 electrolytes. X-ray powder diffraction is used as a new tool to estimate the crystallinity of chelates as well as to elucidate their geometrical structures.

  4. Thermodynamic Modeling of Poorly Complexing Metals in Concentrated Electrolyte Solutions: An X-Ray Absorption and UV-Vis Spectroscopic Study of Ni(II) in the NiCl2-MgCl2-H2O System

    Science.gov (United States)

    Zhang, Ning; Brugger, Joël; Etschmann, Barbara; Ngothai, Yung; Zeng, Dewen

    2015-01-01

    Knowledge of the structure and speciation of aqueous Ni(II)-chloride complexes is important for understanding Ni behavior in hydrometallurgical extraction. The effect of concentration on the first-shell structure of Ni(II) in aqueous NiCl2 and NiCl2-MgCl2 solutions was investigated by Ni K edge X-ray absorption (XAS) and UV-Vis spectroscopy at ambient conditions. Both techniques show that no large structural change (e.g., transition from octahedral to tetrahedral-like configuration) occurs. Both methods confirm that the Ni(II) aqua ion (with six coordinated water molecules at RNi-O = 2.07(2) Å) is the dominant species over the whole NiCl2 concentration range. However, XANES, EXAFS and UV-Vis data show subtle changes at high salinity (> 2 mol∙kg-1 NiCl2), which are consistent with the formation of small amounts of the NiCl+ complex (up to 0.44(23) Cl at a Ni-Cl distance of 2.35(2) Å in 5.05 mol∙kg-1 NiCl2) in the pure NiCl2 solutions. At high Cl:Ni ratio in the NiCl2-MgCl2-H2O solutions, small amounts of [NiCl2]0 are also present. We developed a speciation-based mixed-solvent electrolyte (MSE) model to describe activity-composition relationships in NiCl2-MgCl2-H2O solutions, and at the same time predict Ni(II) speciation that is consistent with our XAS and UV-Vis data and with existing literature data up to the solubility limit, resolving a long-standing uncertainty about the role of chloride complexing in this system. PMID:25885410

  5. Thermodynamic modeling of poorly complexing metals in concentrated electrolyte solutions: an X-ray absorption and UV-Vis spectroscopic study of Ni(II in the NiCl2-MgCl2-H2O system.

    Directory of Open Access Journals (Sweden)

    Ning Zhang

    Full Text Available Knowledge of the structure and speciation of aqueous Ni(II-chloride complexes is important for understanding Ni behavior in hydrometallurgical extraction. The effect of concentration on the first-shell structure of Ni(II in aqueous NiCl2 and NiCl2-MgCl2 solutions was investigated by Ni K edge X-ray absorption (XAS and UV-Vis spectroscopy at ambient conditions. Both techniques show that no large structural change (e.g., transition from octahedral to tetrahedral-like configuration occurs. Both methods confirm that the Ni(II aqua ion (with six coordinated water molecules at RNi-O = 2.07(2 Å is the dominant species over the whole NiCl2 concentration range. However, XANES, EXAFS and UV-Vis data show subtle changes at high salinity (> 2 mol∙kg(-1 NiCl2, which are consistent with the formation of small amounts of the NiCl+ complex (up to 0.44(23 Cl at a Ni-Cl distance of 2.35(2 Å in 5.05 mol∙kg(-1 NiCl2 in the pure NiCl2 solutions. At high Cl:Ni ratio in the NiCl2-MgCl2-H2O solutions, small amounts of [NiCl2]0 are also present. We developed a speciation-based mixed-solvent electrolyte (MSE model to describe activity-composition relationships in NiCl2-MgCl2-H2O solutions, and at the same time predict Ni(II speciation that is consistent with our XAS and UV-Vis data and with existing literature data up to the solubility limit, resolving a long-standing uncertainty about the role of chloride complexing in this system.

  6. VELOCITY-RESOLVED [C ii] EMISSION AND [C ii]/FIR MAPPING ALONG ORION WITH HERSCHEL *,**

    Science.gov (United States)

    Goicoechea, Javier R.; Teyssier, D.; Etxaluze, M.; Goldsmith, P.F.; Ossenkopf, V.; Gerin, M.; Bergin, E.A.; Black, J.H.; Cernicharo, J.; Cuadrado, S.; Encrenaz, P.; Falgarone, E.; Fuente, A.; Hacar, A.; Lis, D.C.; Marcelino, N.; Melnick, G.J.; Müller, H.S.P.; Persson, C.; Pety, J.; Röllig, M.; Schilke, P.; Simon, R.; Snell, R.L.; Stutzki, J.

    2015-01-01

    We present the first ~7.5′×11.5′ velocity-resolved (~0.2 km s−1) map of the [C ii] 158 μm line toward the Orion molecular cloud 1 (OMC 1) taken with the Herschel/HIFI instrument. In combination with far-infrared (FIR) photometric images and velocity-resolved maps of the H41α hydrogen recombination and CO J=2-1 lines, this data set provides an unprecedented view of the intricate small-scale kinematics of the ionized/PDR/molecular gas interfaces and of the radiative feedback from massive stars. The main contribution to the [C ii] luminosity (~85 %) is from the extended, FUV-illuminated face of the cloud (G0>500, nH>5×103 cm−3) and from dense PDRs (G≳104, nH≳105 cm−3) at the interface between OMC 1 and the H ii region surrounding the Trapezium cluster. Around ~15 % of the [C ii] emission arises from a different gas component without CO counterpart. The [C ii] excitation, PDR gas turbulence, line opacity (from [13C ii]) and role of the geometry of the illuminating stars with respect to the cloud are investigated. We construct maps of the L[C ii]/LFIR and LFIR/MGas ratios and show that L[C ii]/LFIR decreases from the extended cloud component (~10−2–10−3) to the more opaque star-forming cores (~10−3–10−4). The lowest values are reminiscent of the “[C ii] deficit” seen in local ultra-luminous IR galaxies hosting vigorous star formation. Spatial correlation analysis shows that the decreasing L[C ii]/LFIR ratio correlates better with the column density of dust through the molecular cloud than with LFIR/MGas. We conclude that the [C ii] emitting column relative to the total dust column along each line of sight is responsible for the observed L[C ii]/LFIR variations through the cloud. PMID:26568638

  7. VELOCITY-RESOLVED [C ii] EMISSION AND [C ii]/FIR MAPPING ALONG ORION WITH HERSCHEL.

    Science.gov (United States)

    Goicoechea, Javier R; Teyssier, D; Etxaluze, M; Goldsmith, P F; Ossenkopf, V; Gerin, M; Bergin, E A; Black, J H; Cernicharo, J; Cuadrado, S; Encrenaz, P; Falgarone, E; Fuente, A; Hacar, A; Lis, D C; Marcelino, N; Melnick, G J; Müller, H S P; Persson, C; Pety, J; Röllig, M; Schilke, P; Simon, R; Snell, R L; Stutzki, J

    2015-10-10

    We present the first ~7.5'×11.5' velocity-resolved (~0.2 km s -1 ) map of the [C ii] 158 μ m line toward the Orion molecular cloud 1 (OMC 1) taken with the Herschel /HIFI instrument. In combination with far-infrared (FIR) photometric images and velocity-resolved maps of the H41 α hydrogen recombination and CO J =2-1 lines, this data set provides an unprecedented view of the intricate small-scale kinematics of the ionized/PDR/molecular gas interfaces and of the radiative feedback from massive stars. The main contribution to the [C ii] luminosity (~85 %) is from the extended, FUV-illuminated face of the cloud ( G 0 >500, n H >5×10 3 cm -3 ) and from dense PDRs ( G ≳10 4 , n H ≳10 5 cm -3 ) at the interface between OMC 1 and the H ii region surrounding the Trapezium cluster. Around ~15 % of the [C ii] emission arises from a different gas component without CO counterpart. The [C ii] excitation, PDR gas turbulence, line opacity (from [ 13 C ii]) and role of the geometry of the illuminating stars with respect to the cloud are investigated. We construct maps of the L [C ii]/ L FIR and L FIR / M Gas ratios and show that L [C ii]/ L FIR decreases from the extended cloud component (~10 -2 -10 -3 ) to the more opaque star-forming cores (~10 -3 -10 -4 ). The lowest values are reminiscent of the "[C ii] deficit" seen in local ultra-luminous IR galaxies hosting vigorous star formation. Spatial correlation analysis shows that the decreasing L [C ii]/ L FIR ratio correlates better with the column density of dust through the molecular cloud than with L FIR / M Gas . We conclude that the [C ii] emitting column relative to the total dust column along each line of sight is responsible for the observed L [C ii]/ L FIR variations through the cloud.

  8. Cytotoxic effect of inositol hexaphosphate and its Ni(II) complex on human acute leukemia Jurkat T cells.

    Science.gov (United States)

    de Lima, Eliane May; Kanunfre, Carla Cristine; de Andrade, Lucas Ferrari; Granato, Daniel; Rosso, Neiva Deliberali

    2015-12-01

    Inositol hexaphosphate (InsP6) is present in cereals, legumes, nuts and seed oils and is biologically active against some tumor and cancer cells. Herein, this study aimed at evaluating the cellular toxicity, antiproliferative activity and effects on cell cycle progression of free InsP6 and InsP6-Ni(II) of leukemic T (Jurkat) and normal human cells. Treatments with InsP6 at concentrations between 1.0 and 4.0mM significantly decreased the viability of Jurkat cells, but showed no cytotoxic effect on normal human lymphocytes. Treatment with InsP6-Ni(II) complex at concentrations between 0.05 and 0.30 mM showed an anti-proliferative dose and a time-dependent effect, with significantly reduced cell viability of Jurkat cells but showed no cytotoxic effect on normal human lymphocytes as compared to the control. Ni(II) free ion was toxic to normal cells while InsP6-Ni(II) had no cytotoxic effect. The InsP6-Ni(II) complex potentiated (up to 10×) the antiproliferative effect of free InsP6 on Jurkat cells. The cytometric flow assay showed that InsP6 led to an accumulation of cells in the G0/G1 phase of the cell cycle, accompanied by a decrease in the number of cells in S and G2/M phases, whereas InsP6-Ni(II) has led to an accumulation of cells in the S and G2/M phases. Our findings showed that InsP6-Ni(II) potentiates cytotoxic effects of InsP6 on Jurkat cells and may be a potential adjuvant in the treatment of cancer. Copyright © 2015 Elsevier B.V. All rights reserved.

  9. Theoretical study of heavy metal Cd, Cu, Hg, and Ni(II) adsorption on the kaolinite(0 0 1) surface

    International Nuclear Information System (INIS)

    Zhao, Jian; He, Man-Chao

    2014-01-01

    Highlights: • We investigated the adsorption of Cd, Cu, Hg, and Ni(II) on kaolinite(0 0 1) surface. • The adsorption capabilities of the kaolinite for HM atoms were Ni > Cu > Cd > Hg(II). • The adsorption energy increases with the coverage for Cd, Cu, and Hg(II) atoms. • The adsorption energy decreases with the coverage for Ni(II) atoms. - Abstract: Heavy metal pollution is currently of great concern because it has been recognized as a potential threat to air, water, and soil. Adsorption was one of the most popular methods for the removal of heavy metal. The adsorption of heavy metal Cd, Cu, Hg, and Ni(II) atoms on the hydroxylated (0 0 1) surface of kaolinite was investigated using density-functional theory within the generalized gradient approximation and a supercell approach. The coverage dependence of the adsorption structures and energetics were systematically studied for a wide range of coverage Θ [from 0.11 to 1.0 monolayers (ML)] and adsorption sites. The most stable among all possible adsorption sites for Cd(II) atom was the two-fold bridge site followed by the one-fold top site, and the top site was the most favorite adsorption site for Cu and Ni(II) atoms, while the three-fold hollow site was the most stable adsorption site for Hg(II) atom followed by the two-fold bridge site. The adsorption energy increases with the coverage for Cd, Cu, and Hg(II) atoms, thus indicating the higher stability of surface adsorption and a tendency to the formation of adsorbate islands (clusters) with increasing the coverage. However, the adsorption energy of Ni(II) atoms decreases when increasing the coverage. The adsorption capabilities of the kaolinite clay for the heavy metal atoms were in the order of Ni > Cu > Cd > Hg(II). The other properties of the Cd, Cu, Hg, and Ni(II)/kaolinite(0 0 1) system including the different charge distribution, the lattice relaxation, and the electronic density of states were also studied and discussed in detail

  10. Enthalpic Contribution of Ni(II) in the Interaction between Carbonaceous Material and Aqueous Solution

    OpenAIRE

    Liliana Giraldo; Juan Carlos Moreno-Piraján

    2017-01-01

    Solid adsorbents were prepared from corn cob that was modified with a solution of HNO3 6 M at different contact times. The solids are characterized by physical N2 adsorption at 77 K to know their surface area by applying the BET model and surface chemistry is determined using the Bohem method. Once we have prepared the adsorbents we determine the immersion enthalpy, ΔHim, of the solids in Ni(II) aqueous solutions of different concentrations between 20 and 800 mg·L−1, with values for ΔHim betw...

  11. Determination of Ni(II) crystal structure by powder x-ray diffraction ...

    African Journals Online (AJOL)

    X-ray powder diffraction pattern was used to determine the length of the unit cell, “a”, the lattice structure type, and the number of atoms per unit cell of Ni(II) crystal. The “a” value was determined to be 23.66 ± 0.005 Å, particle size of 34.87 nm, volume 13.24 Å and Strain value ε = 9.8 x 10-3. The cell search on PXRD patterns ...

  12. Crystal Structures, Properties and Reactivity of Selected Macrocyclic and Chelate Complexes of Ni(II)

    OpenAIRE

    Churchard, Andrew James

    2012-01-01

    In this dissertation we describe the structure, properties and decomposition reactions of a series of Ni(II) coordination complexes formed from reaction of the appropriate macrocyclic or chelating ligand with a simple nickel salt. The ligands used were 12aneS4 (1,4,7,10-tetrathiacyclododecane), 14aneS4 (1,4,8,11-tetrathiacyclotetradecane), cyclam (1,4,8,11-tetraazacyclotetradecane), dppe (1,2- (diphenylphosphino)ethane), and PP3 (tris-(2-(diphenylphosphino)ethyl)phosphine). The wo...

  13. Coordination behavior of tetraaza [N4] ligand towards Co(II), Ni(II), Cu(II), Cu(I) and Pd(II) complexes: Synthesis, spectroscopic characterization and anticancer activity

    Science.gov (United States)

    El-Boraey, Hanaa A.

    2012-11-01

    Novel eight Co(II), Ni(II), Cu(II), Cu(I) and Pd(II) complexes with [N4] ligand (L) i.e. 2-amino-N-{2-[(2-aminobenzoyl)amino]ethyl}benzamide have been synthesized and structurally characterized by elemental analysis, spectral, thermal (TG/DTG), magnetic, and molar conductivity measurements. On the basis of IR, mass, electronic and EPR spectral studies an octahedral geometry has been proposed for Co(II), Ni(II) complexes and Cu(II) chloride complex, square-pyramidal for Cu(I) bromide complex. For Cu(II) nitrate complex (6), Pd(II) complex (8) square planar geometry was proposed. The EPR data of Cu(II) complexes in powdered form indicate dx2-y2 ground state of Cu(II) ion. The antitumor activity of the synthesized ligand and some selected metal complexes has been studied. The palladium(II) complex (8) was found to display cytotoxicity (IC50 = 25.6 and 41 μM) against human breast cancer cell line MCF-7 and human hepatocarcinoma HEPG2 cell line.

  14. Synthesis and Characterization of Some New Cu(II, Ni(II and Zn(II Complexes with Salicylidene Thiosemicarbazones: Antibacterial, Antifungal and in Vitro Antileukemia Activity

    Directory of Open Access Journals (Sweden)

    Tudor Rosu

    2013-07-01

    Full Text Available Thirty two new Cu(II, Ni(II and Zn(II complexes (1–32 with salicylidene thiosemicarbazones (H2L1–H2L10 were synthesized. Salicylidene thiosemicarbazones, of general formula (XN-NH-C(S-NH(Y, were prepared through the condensation reaction of 2-hydroxybenzaldehyde and its derivatives (X with thiosemicarbazide or 4-phenylthiosemicarbazide (Y = H, C6H5. The characterization of the new formed compounds was done by 1H-NMR, 13C-NMR, IR spectroscopy, elemental analysis, magnetochemical, thermoanalytical and molar conductance measurements. In addition, the structure of the complex 5 has been determined by X-ray diffraction method. All ligands and metal complexes were tested as inhibitors of human leukemia (HL-60 cells growth and antibacterial and antifungal activities.

  15. Synthesis, Spectral and Antimicrobial Studies of Some Co(II, Ni(II and Cu(II Complexes Containing 2-Thiophenecarboxaldehyde Moiety

    Directory of Open Access Journals (Sweden)

    A. P. Mishra

    2012-01-01

    Full Text Available Some new Schiff base metal complexes of Co(II, Ni(II and Cu(II derived from 3-chloro-4-fluoroaniline (HL1 and 4-fluoroaniline (HL2 with 2-thiophenecarboxaldehyde have been synthesized and characterized by elemental analysis, FT-IR, FAB-mass, molar conductance, electronic spectra, ESR and magnetic susceptibility. The complexes exhibit coordination number 4 or 6. The complexes are colored and stable in air. Analytical data revealed that all the complexes exhibited 1:2 (metal: ligand ratio. FAB-mass data show degradation pattern of the complexes. The Schiff base and metal complexes show a good activity against the bacteria; B. subtilis, E. coli and S. aureus and fungi A. niger, A. flavus and C. albicans. The antimicrobial results also indicate that the metal complexes are better antimicrobial agents as compared to the Schiff bases.

  16. Ionophoretic method in the study of mixed ligand ternary chelates of UO2(II), Ni(II) and Zn(II) involving nitrilotriacetate and cytosine as ligands

    International Nuclear Information System (INIS)

    Mishra, A.P.; Mishra, S.K.; Yadava, K.L.

    1987-01-01

    A novel electrophoretic technique is described for the assessment of the equilibria in mixed-ligand complex system in solution. It is based on the movement of spot of the metal ion under an electric field with the complexants added in the background electrolyte at fixed pH. The concentration of primary ligand nitrilotriacetate was constant while that of secondary ligand (cytosine) was varied. The plot of log (cytosine) against mobility was used to obtain information on the formation of the mixed complexes and to calculate its stability constants. Experimentally obtained logK values are as 5.62, 4.55 and 4.42 for mixed complexes of UO 2 (II), Ni(II) and Zn(II) respectively at μ=0.1 and temp.=35 +- 01.degC. (author). 10 refs

  17. STUDIES OF MN (II) AND NI (II) COMPLEXES WITH SCHIFF BASE ...

    African Journals Online (AJOL)

    DR. AMINU

    2010-06-01

    Jun 1, 2010 ... The solubility test on the Schiff base and its nickel(II) complex revealed their solubility in most organic solvents ... Chemicals of analytical grade purity were used. Melting point and decomposition temperature were ... stirring bar and sodium salt of the Schiff base, prepared by neutralizing a known quantity of ...

  18. Studies of Mn (II) and Ni (II) complexes with Schiff base derived from ...

    African Journals Online (AJOL)

    However, manganese(II) complex is insoluble in most organic solvents but soluble in dimethylsulphoxide (DMSO). The molar conductance of the complexes measured are low, indicating their non-electrolytic nature. The potentiometric and spectrophotometric studies of the complex compounds revealed 1:1 metal to ligand ...

  19. Studies of mn (ii) and ni (ii) complexes with schiff base derived from ...

    African Journals Online (AJOL)

    However, manganese(II) complex is insoluble in most organic solvents but soluble in dimethylsulphoxide (DMSO). The molar conductance of the complexes measured are, indicating their non-electrolytic nature. The potentiometric and spectrophotometric studies of the complex compounds revealed 1:1 metal to ligand ratio.

  20. The Origins of [C ii] Emission in Local Star-forming Galaxies

    Energy Technology Data Exchange (ETDEWEB)

    Croxall, K. V. [Department of Astronomy, The Ohio State University, 4051 McPherson Laboratory, 140 W. 18th Avenue, Columbus, OH, 43210 (United States); Smith, J. D. [Max-Planck-Institut fur Astronomie, Königstuhl 17, D-69117 Heidelberg (Germany); Pellegrini, E. [Department of Physics and Astronomy, University of Toledo, 2801 W. Bancroft Street, Toledo, OH 43606 (United States); Groves, B. [Research School of Astronomy and Astrophysics, Australian National University, Cotter Road, Weston, ACT 2611 (Australia); Bolatto, A.; Wolfire, M. G. [Department of Astronomy, University of Maryland, College Park, MD 20742 (United States); Herrera-Camus, R. [Max-Planck-Institut für extraterrestrische Physik, Giessen-bachstr., D-85748 Garching (Germany); Sandstrom, K. M. [Center for Astrophysics and Space Sciences, Department of Physics, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093 (United States); Draine, B. [Department of Astrophysical Sciences, Princeton University, Princeton, NJ 08544 (United States); Armus, L. [Spitzer Science Center, California Institute of Technology, MC 314-6, Pasadena, CA 91125 (United States); Boquien, M. [Unidad de Astronomía, Fac. Cs. Básicas, Universidad de Antofagasta, Avda. U. de Antofagasta 02800, Antofagasta (Chile); Brandl, B. [Leiden Observatory, Leiden University, P.O. Box 9513, 2300 RA Leiden (Netherlands); Dale, D. [Department of Physics and Astronomy, University of Wyoming, Laramie, WY 82071 (United States); Galametz, M. [Laboratoire AIM-Paris-Saclay, CEA/DSM/Irfu—CNRS—Université Paris Diderot, CEA-Saclay, 91191, Gif-sur-Yvette (France); Hunt, L., E-mail: jd.smith@utoledo.edu [INAF-Osservatorio Astrofisico di Arcetri, Largo E. Fermi 5, I-50125, Firenze (Italy); and others

    2017-08-20

    The [C ii] 158 μ m fine-structure line is the brightest emission line observed in local star-forming galaxies. As a major coolant of the gas-phase interstellar medium, [C ii] balances the heating, including that due to far-ultraviolet photons, which heat the gas via the photoelectric effect. However, the origin of [C ii] emission remains unclear because C{sup +} can be found in multiple phases of the interstellar medium. Here we measure the fractions of [C ii] emission originating in the ionized and neutral gas phases of a sample of nearby galaxies. We use the [N ii] 205 μ m fine-structure line to trace the ionized medium, thereby eliminating the strong density dependence that exists in the ratio of [C ii]/[N ii] 122 μ m. Using the FIR [C ii] and [N ii] emission detected by the KINGFISH (Key Insights on Nearby Galaxies: a Far- Infrared Survey with Herschel ) and Beyond the Peak Herschel programs, we show that 60%–80% of [C ii] emission originates from neutral gas. We find that the fraction of [C ii] originating in the neutral medium has a weak dependence on dust temperature and the surface density of star formation, and has a stronger dependence on the gas-phase metallicity. In metal-rich environments, the relatively cooler ionized gas makes substantially larger contributions to total [C ii] emission than at low abundance, contrary to prior expectations. Approximate calibrations of this metallicity trend are provided.

  1. Synthesis, spectroscopic characterization, molecular modeling and potentiometric studies of Co(II), Ni(II), Cu(II) and Zn(II) complexes with 1,1-diaminobutane-Schiff base

    Science.gov (United States)

    Alaghaz, Abdel-Nasser M. A.

    2014-08-01

    Complexes of cobalt(II), nickel(II), copper(II) and zinc(II) of general composition [M(L)(H2O)2]·2H2O have been synthesized [L = N,N";-bis(2-hydroxybenzylidene)-1,1-diaminobutane]. The elemental analysis, molar conductance measurements, magnetic susceptibility measurements, mass, IR, UV, NMR, SEM, EDX, thermal and EPR spectral studies of the compounds led to the conclusion that the ligand acts as a tetradentate manner. The molar conductance of the complexes in fresh solution of DMSO lies in the range of 7.46-9.13 Ω-1 cm2 mol-1 indicating their non-electrolytic behavior. On the basis of analytical and spectroscopic techniques, octahedral geometry of the complexes was proposed. The Schiff base acts as tetradentate ligand, coordinated through deprotonated phenolic oxygen and azomethine nitrogen atoms. The ligand field parameters were calculated for Co(II), Ni(II) and Cu(II) complexes and their values were found in the range reported for a octahedral structure. The molecular parameters of the ligand and its Co(II), Ni(II), Cu(II) and Zn(II) complexes have been calculated. Protonation constants of Schiff base and stability constants of their binary metal complexes have been determined potentiometrically in 50% DMSO-water media at 25 °C and ionic strength 0.10 M sodium perchlorate.

  2. Fe (III), Co(II), Ni(II), Cu(II) and Zn(II) complexes of schiff bases based-on glycine and phenylalanine: Synthesis, magnetic/thermal properties and antimicrobial activity

    Science.gov (United States)

    Sevgi, Fatih; Bagkesici, Ugur; Kursunlu, Ahmed Nuri; Guler, Ersin

    2018-02-01

    Zinc (II), copper (II), nickel (II), cobalt (II) and iron (III) complexes of Schiff bases (LG, LP) derived from 2-hydroxynaphthaldehyde with glycine and phenylalanine were reported and characterized by 1H NMR, 13C NMR, elemental analyses, melting point, FT-IR, magnetic susceptibility and thermal analyses (TGA). TGA data show that iron and cobalt include to the coordinated water and metal:ligand ratio is 1:2 while the complex stoichiometry for Ni (II), Cu (II) and Zn (II) complexes is 1:1. As expected, Ni (II) and Zn (II) complexes are diamagnetic; Cu (II), Co (II) and Fe (III) complexes are paramagnetic character due to a strong ligand of LG and LP. The LG, LP and their metal complexes were screened for their antimicrobial activities against five Gram-positive (Staphylococcus aureus, Methicillin resistant Staphylococcus aureus (MRSA), Bacillus cereus, Streptococcus mutans and Enterococcus faecalis) and three Gram-negative (Escherichia coli, Klebsiella pneumoniae and Pseudomonas aeruginosa) and one fungi (Candida albicans) by using broth microdilution techniques. The activity data show that ligands and their metal complexes exhibited moderate to good activity against Gram-positive bacteria and fungi.

  3. Adsorption and co-adsorption of graphene oxide and Ni(II) on iron oxides: A spectroscopic and microscopic investigation.

    Science.gov (United States)

    Sheng, Guodong; Huang, Chengcai; Chen, Guohe; Sheng, Jiang; Ren, Xuemei; Hu, Baowei; Ma, Jingyuan; Wang, Xiangke; Huang, Yuying; Alsaedi, Ahmed; Hayat, Tasawar

    2018-02-01

    Graphene oxide (GO) may strongly interact with toxic metal ions and mineral particles upon release into the soil environment. We evaluated the mutual effects between GO and Ni (Ni(II)) with regard to their adsorption and co-adsorption on two minerals (goethite and hematite) in aqueous phase. Results indicated that GO and Ni could mutually facilitate the adsorption of each other on both goethite and hematite over a wide pH range. Addition of Ni promoted GO co-adsorption mainly due to the increased positive charge of minerals and cation-π interactions, while the presence of GO enhanced Ni co-adsorption predominantly due to neutralization of positive charge and strong interaction with oxygen-containing functional groups on adsorbed GO. Increasing adsorption of GO and Ni on minerals as they coexist may thus reduce their mobility in soil. Extended X-ray absorption fine structure (EXAFS) spectroscopy data revealed that GO altered the microstructure of Ni on minerals, i.e., Ni formed edge-sharing surface species (at R Ni-Fe ∼3.2 Å) without GO, while a GO-bridging ternary surface complexes (at R Ni-C ∼2.49 Å and R Ni-Fe ∼4.23 Å) was formed with GO. These findings improved the understanding of potential fate and toxicity of GO as well as the partitioning processes of Ni ions in aquatic and soil environments. Copyright © 2017 Elsevier Ltd. All rights reserved.

  4. Synthesis, NMR characterization, X-ray crystal structure of Co(II) Ni(II) and Cu(II) complexes of a pyridine containing self-assembling

    International Nuclear Information System (INIS)

    Ranjbar, M.; Taghavipour, M.; Moghimi, A.; Aghabozorg, H.

    2002-01-01

    In the recent years, the self-assembling systems have been attracted chemists. The intermolecular bond in such systems mainly consists of ion pairing and hydrogen bonding [1,2]. The reaction between self-assembling system liquid LH 2 (py dc=2,6-pyridinedicarboxylic acid and py da=2,6- pyridine diamin) with cobalt (II) nitrate, nickel (II) chloride, and copper (II) acetate in water leads to the formation of self- assemble coordination complexes, [py da.H] 2 [M(py dc) 2 ]. H 2 O, M=Co(II),Ni(II), and Cu(II). The characterization was performed using elemental analysis, ESI mass spectroscopy, 1 H and 13 C NMR and X-ray crystallography. The crystal systems are monoclinic with space group P2 1 /n and four molecules per unit cell. These complexes shows 13 C NMR resonances of cationic counter ion [(py dc,H)] + in DMSO- d 6 but no signal corresponding to the two coordinated ligands [py dc] 2- The metal atoms are six-coordinated with a distorted octahedral geometry. The two [py de] 2- units are almost perpendicular to each other

  5. Variability of Fe II Emission Features in the Seyfert 1 Galaxy NGC 5548

    DEFF Research Database (Denmark)

    Vestergaard, Marianne; Peterson, B. M.

    2005-01-01

    We study the low-contrast Fe II emission blends in the ultraviolet (1250--2200A) and optical (4000--6000A) spectra of the Seyfert 1 galaxy NGC 5548 and show that these features vary in flux and that these variations are correlated with those of the optical continuum. The amplitude of variability...... of the optical Fe II emission is 50% - 75% that of Hbeta and the ultraviolet Fe II emission varies with an even larger amplitude than Hbeta. However, accurate measurement of the flux in these blends proves to be very difficult even using excellent Fe II templates to fit the spectra. We are able to constrain only...... weakly the optical Fe II emission-line response timescale to a value less than several weeks; this upper limit exceeds all the reliably measured emission-line lags in this source so it is not particularly meaningful. Nevertheless, the fact that the optical Fe II and continuum flux variations...

  6. Enthalpic Contribution of Ni(II in the Interaction between Carbonaceous Material and Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Liliana Giraldo

    2017-01-01

    Full Text Available Solid adsorbents were prepared from corn cob that was modified with a solution of HNO3 6 M at different contact times. The solids are characterized by physical N2 adsorption at 77 K to know their surface area by applying the BET model and surface chemistry is determined using the Bohem method. Once we have prepared the adsorbents we determine the immersion enthalpy, ΔHim, of the solids in Ni(II aqueous solutions of different concentrations between 20 and 800 mg·L−1, with values for ΔHim between 10.0 and 35.3 J·g−1. From the results obtained for the immersion enthalpy in function of the ion Ni(II concentration we calculate the contribution to the immersion enthalpy that corresponds to the ion when it is treated with the system adsorbent-solution as a mixture in which the solid, the solvent, and the adsorbate are involved. The solution thermodynamics allows for establishing the enthalpic changes that bring the ion in function of the concentration and the intensity of the interaction of solid-metal ion that is favored by the presence of acid groups in the solid.

  7. Determination of Cr, Mn, Si, and Ni in carbon steels by optical emission spectrometry with spark source

    International Nuclear Information System (INIS)

    Garcia Gonzalez, M.A.; Pomares Alfonso, M.; Mora Lopez, L.

    1995-01-01

    Elemental composition of steels determines some important of his characteristic moreover it is necessary to obtain their quality certification. Analytical procedure has performed for determination of Cr, Mn, Si and Ni in carbon steels by optical emission spectrometry with spark source. reproducibility of results is 5-11 %. Exactitude has tested with results that have obtained by internationally recognised methods-

  8. Assessing comparative terrestrial ecotoxicity of Cd, Co, Cu, Ni, Pb, and Zn: The influence of aging and emission source

    DEFF Research Database (Denmark)

    Owsianiak, Mikolaj; Holm, Peter E.; Fantke, Peter

    2015-01-01

    H or soil organic carbon, emission source occasionally has an effect on reactivity of Cd, Co, Cu, Ni, Pb and Zn emitted from various anthropogenic sources followed by aging in the soil from a few years to two centuries. The uncertainties in estimating the age prevent definitive conclusions about...

  9. Solid State C-13 and H-2 NMR Investigations of Paramagnetic Ni(II)(acac)(2)L-2 Complexes

    DEFF Research Database (Denmark)

    Lennartson, A.; Christensen, Lene Ulrikke; McKenzie, C. J.

    2014-01-01

    Nine structurally related paramagnetic acetylacetonato nickel(II) complexes: [Ni(acac)(2)] and trans-[Ni(acac)(2)(X)(2)]nH/D2O, X = H2O, D2O, NH3, MeOH, PMePh2, PMe2Ph, or [dppe](1/2), n = 0 or 1, dppe = 1,2-his(diphenylphosphino)ethane, as well as cis-[Ni(F-6-acac)(2)(D2O)(2)], F-6-acac......[Ni(acac)(2)(PMe2Ph)(2)], trans-[Ni(acac)(2)(PMePh2)(2)], and the noncrystallographically characterized trans-[Ni(acac)(2)(dppe)], were assigned using these correlations. The complexes with L = H2O, D2O, NH3, and MeOH can be prepared by a series of solid state desorption and sorption reactions. Crystal...... structures for trans-[Ni(acac)(2)(NH3)(2)] and trans-[Ni(acac)(2)(PMePh2)(2)] are reported....

  10. Synthesis and characterization of Ni(II, Cu(II and Co(III complexes with polyamine-containing macrocycles bearing an aminoethyl pendant arm

    Directory of Open Access Journals (Sweden)

    K. S. SIDDIQI

    2004-09-01

    Full Text Available Reaction of [M(ppn2]X2 (where M = Cu(II, Ni(II, Co(II and ppn = 1,3-diaminopropane with formaldehyde and ethylenediamine in methanol results in the ready formation of a 16-membered macrocyclic complex. The complexes were characterized by elemental anlysis, IR, EPR, electronic spectral data, magnetic moments and conductance measurements. The Cu(II, Ni(II and Co(III complexes are coordinated axially with both pendant groups of the hexadentate macrocycle. These pendant donors are attached to the macrocycle by a carbon chain. The electrical conductivities of the Cu(II and Ni(II chelates indicated them to be 1:2 electrolytes whilst those of Co(III is a 1:3 electrolyte in DMSO. The EPR spectrum of the copper complex exhibited G at 3.66, which indicates a considerable exchange interaction in the complex. Spectroscopic evidence suggests that in all of the complexes the metal ion is in an octahedral environment.

  11. Synthesis and characterization of VO(II), Co(II), Ni(II), Cu(II) and Zn(II) complexes of chromone based azo-linked Schiff base ligand.

    Science.gov (United States)

    Anitha, C; Sheela, C D; Tharmaraj, P; Johnson Raja, S

    2012-12-01

    Azo-Schiff-base complexes of VO(II), Co(II), Ni(II), Cu(II) and Zn(II) have been synthesized and characterized by elemental analysis, IR, UV-Vis, (1)H NMR, mass spectra, molar conductance, magnetic susceptibility measurement, electron spin resonance (EPR), CV, fluorescence, NLO and SEM. The conductance data indicate the nonelectrolytic nature of the complexes, except VO(II) complex which is electrolytic in nature. On the basis of electronic spectra and magnetic susceptibility octahedral geometry has been proposed for the complexes. The EPR spectra of copper and oxovanadium complexes in DMSO at 300 and 77K were recorded and its salient features are reported. The redox behavior of the copper(II) complex was studied using cyclic voltammetry. The in vitro antimicrobial activity against Staphylococcus aureus, Escherichia coli, Salmonella enterica typhi, Bacillus subtilis and Candida strains was studied and compared with that of free ligand by well-diffusion technique. The azo Schiff base exhibited fluorescence properties originating from intraligand (π-π(*)) transitions and metal-mediated enhancement is observed on complexation and so the synthesized complexes can serve as potential photoactive materials as indicated from their characteristic fluorescence properties. On the basis of the optimized structures, the second-order nonlinear optical properties (NLO) are calculated by using second-harmonic generation (SHG) and also the surface morphology of the complexes was studied by SEM. Copyright © 2012 Elsevier B.V. All rights reserved.

  12. Ca II H and K emission from late-type stars

    International Nuclear Information System (INIS)

    Middlekoop, F.

    1982-01-01

    This thesis is based on a study of the Ca II H and K emission features of late main-sequence stars. In Chapter II it is shown that rotation periods can be determined from a modulation in the Ca II H and K signal for many stars in a broad range of spectral types. In Chapter III it is shown that a clear correlation exists between Ca II H and K emission and rotational velocity in active main-sequence stars. There is an indication for a (probably colour-dependent) critical velocity at which the Ca II H and K emission suddenly drops. Chapter IV discusses the dependence of Ca II H and K emission on the rotation rate for evolved stars. (Auth./C.F.)

  13. Indolenine meso-substituted dibenzotetraaza[14]annulene and its coordination chemistry toward the transition metal ions Mn(III), Fe(III), Co(II), Ni(II), Cu(II), and Pd(II).

    Science.gov (United States)

    Khaledi, Hamid; Olmstead, Marilyn M; Ali, Hapipah Mohd; Thomas, Noel F

    2013-02-18

    A new dibenzotetraaza[14]annulene bearing two 3,3-dimethylindolenine fragments at the meso positions (LH(2)), has been synthesized through a nontemplate method. X-ray crystallography shows that the whole molecule is planar. The basicity of the indolenine ring permits the macrocycle to be protonated external to the core and form LH(4)(2+)·2Cl(-). Yet another structural modification having strong C-H···π interactions was found in the chloroform solvate of LH(2). The latter two modifications are accompanied by a degree of nonplanar distortion. The antiaromatic core of the macrocycle can accommodate a number of metal ions, Mn(III), Fe(III), Co(II), Ni(II) and Cu(II), to form complexes of [Mn(L)Br], [Mn(L)Cl], [Fe(LH(2))Cl(2)](+)·Cl(-), [Co(L)], [Ni(L)], and [Cu(L)]. In addition, the reaction of LH(2) with the larger Pd(II) ion leads to the formation of [Pd(2)(LH(2))(2)(OAc)(4)] wherein the macrocycle acts as a semiflexible ditopic ligand to coordinate pairs of metal ions via its indolenine N atoms into dinuclear metallocycles. The compounds LH(2), [Co(L)], and [Ni(L)] are isostructural and feature close π-stacking as well as linear chain arrangements in the case of the metal complexes. Variable temperature magnetic susceptibility measurements showed thermally induced paramagnetism in [Ni(L)].

  14. Adsorption of Cu(II), Co(II), and Ni(II) ions by modified magnetic chitosan chelating resin.

    Science.gov (United States)

    Monier, M; Ayad, D M; Wei, Y; Sarhan, A A

    2010-05-15

    Cross-linked magnetic chitosan-isatin Schiff's base resin (CSIS) was prepared for adsorption of metal ions. CSIS obtained was investigated by means of FTIR, (1)H NMR, wide-angle X-ray diffraction (WAXRD), magnetic properties and thermogravimetric analysis (TGA). The adsorption properties of cross-linked magnetic CSIS resin toward Cu(2+), Co(2+) and Ni(2+) ions were evaluated. Various factors affecting the uptake behavior such as contact time, temperature, pH and initial concentration of the metal ions were investigated. The kinetic parameters were evaluated utilizing the pseudo-first-order and pseudo-second-order. The equilibrium data were analyzed using the Langmuir, Freundlich, and Tempkin isotherm models. The adsorption kinetics followed the mechanism of the pseudo-second-order equation for all systems studied, evidencing chemical sorption as the rate-limiting step of adsorption mechanism and not involving a mass transfer in solution. The best interpretation for the equilibrium data was given by Langmuir isotherm, and the maximum adsorption capacities were 103.16, 53.51, and 40.15mg/g for Cu(2+), Co(2+) and Ni(2+) ions, respectively. Cross-linked magnetic CSIS displayed higher adsorption capacity for Cu(2+) in all pH ranges studied. The adsorption capacity of the metal ions decreased with increasing temperature. The metal ion-loaded cross-linked magnetic CSIS were regenerated with an efficiency of greater than 88% using 0.01-0.1M ethylendiamine tetraacetic acid (EDTA). Copyright (c) 2010 Elsevier B.V. All rights reserved.

  15. On the ortho-positronium quenching reactions promoted by Fe(II), Fe(III), Co(III), Ni(II), Zn(II) and Cd(II) cyanocomplexes

    Science.gov (United States)

    Fantola Lazzarini, Anna L.; Lazzarini, Ennio

    The o-Ps quenching reactions promoted in aqueous solutions by the following six cyanocomplexes: [Fe(CN) 6] 4-; [Co(CN) 6] 3-; [Zn(CN) 4] 2-; [Cd(CN) 6] 2-; [Fe(CN) 6] 3-; [Ni(CN) 4] 2- were investigated. The first four reactions probably consist in o-Ps addition across the CN bond, their rate constants at room temperature, Tr, being ⩽(0.04±0.02) × 10 9 M -1 s -1, i.e. almost at the limit of experimental errors. The rate constant of the fifth reaction, in o-Ps oxydation, at Tr is (20.3±0.4) × 10 9 M -1 s -1. The [Ni(CN) 4] 2-k value at Tr, is (0.27±0.01) × 10 9 M -1 s -1, i.e. 100 times less than the rate constants of o-Ps oxydation, but 10 times larger than those of the o-Ps addition across the CN bond. The [Ni(CN) 4] 2- reaction probably results in formation of the following positronido complex: [Ni(CN) 4Ps] 2-. However, it is worth noting that the existence of such a complex is only indirectly deduced. In fact it arises from comparison of the [Ni(CN) 4] 2- rate constant with those of the Fe(II), Zn(II), Cd(II), and Co(III) cyanocomplexes, which, like the Ni(II) cyanocomplex, do not promote o-Ps oxydation or spin exchange reactions.

  16. THE SURVEY OF LINES IN M31 (SLIM): INVESTIGATING THE ORIGINS OF [C II] EMISSION

    Energy Technology Data Exchange (ETDEWEB)

    Kapala, M. J.; Sandstrom, K.; Groves, B.; Kreckel, K.; Schinnerer, E.; Walter, F.; Fouesneau, M. [Max Planck Institut für Astronomie, Königstuhl 17, D-69117 Heidelberg (Germany); Croxall, K. [Department of Astronomy, The Ohio State University, 140 West 18th Avenue, Columbus, OH 43210 (United States); Dalcanton, J. [Department of Astronomy, University of Washington, Box 351580, Seattle, WA 98195 (United States); Leroy, A., E-mail: kapala@mpia.de [National Radio Astronomy Observatory, 520 Edgemont Road, Charlottesville, VA 22903 (United States)

    2015-01-01

    The [C II] 158 μm line is one of the strongest emission lines observed in star-forming galaxies and has been empirically measured to correlate with the star-formation rate (SFR) globally and on kiloparsec scales. However, because of the multiphase origins of [C II], one might expect this relation to break down at small scales. We investigate the origins of [C II] emission by examining high spatial resolution observations of [C II] in M31 with the Survey of Lines in M31. We present five ∼700 × 700 pc (3' × 3') fields mapping the [C II] emission, Hα emission, and the ancillary infrared (IR) data. We spatially separate star-forming regions from diffuse gas and dust emission on ∼50 pc scales. We find that the [C II]-SFR correlation holds even at these scales, although the relation typically has a flatter slope than found at larger (kiloparsec) scales. While the Hα emission in M31 is concentrated in the SFR regions, we find that a significant amount (∼20%-90%) of the [C II] emission comes from outside star-forming regions and that the total IR emission (TIR) has the highest diffuse fraction of all SFR tracers. We find a weak correlation of the [C II]/TIR to dust color in each field and find a large-scale trend of increasing [C II]/TIR with galactocentric radius. The differences in the relative diffuse fractions of [C II], Hα, and IR tracers are likely caused by a combination of energetic photon leakage from H II regions and heating by the diffuse radiation field arising from older (B-star) stellar populations. However, we find that by averaging our measurements over kiloparsec scales, these effects are minimized, and the relation between [C II] and SFR found in other nearby galaxy studies is retrieved.

  17. Secondary Electron Emission Yields from PEP-II Accelerator Materials

    International Nuclear Information System (INIS)

    Kirby, Robert E.

    2000-01-01

    The PEP-II B-Factory at SLAC operates with aluminum alloy and copper vacuum chambers, having design positron and electron beam currents of 2 and 1 A, respectively. Titanium nitride coating of the aluminum vacuum chamber in the arcs of the positron ring is needed in order to reduce undesirable electron-cloud effects. The total secondary electron emission yield of TiN-coated aluminum alloy has been measured after samples of beam chamber material were exposed to air and again after electron-beam bombardment, as a function of incident electron beam angle and energy. The results may be used to simulate and better understand electron-cloud effects under actual operating conditions. We also present yield measurements for other accelerator materials because new surface effects are expected to arise as beam currents increase. Copper, in particular, is growing in popularity for its good thermal conductivity and self-radiation-shielding properties. The effect of electron bombardment, ''conditioning'', on the yield of TiN and copper is shown

  18. New Cu (II), Co(II) and Ni(II) complexes of chalcone derivatives: Synthesis, X-ray crystal structure, electrochemical properties and DFT computational studies

    Science.gov (United States)

    Tabti, Salima; Djedouani, Amel; Aggoun, Djouhra; Warad, Ismail; Rahmouni, Samra; Romdhane, Samir; Fouzi, Hosni

    2018-03-01

    The reaction of nickel(II), copper(II) and cobalt(II) with 4-hydroxy-3-[(2E)-3-(1H-indol-3-yl)prop-2-enoyl]-6-methyl-2H-pyran-2-one (HL) leads to a series of new complexes: Ni(L)2(NH3), Cu(L)2(DMF)2 and Co(L)2(H2O). The crystal structure of the Cu(L)2(DMF)2 complex have been determined by X-ray diffraction methods. The Cu(II) lying on an inversion centre is coordinated to six oxygen atoms forming an octahedral elongated. Additionally, the electrochemical behavior of the metal complexes were investigated by cyclic voltammetry at a glassy carbon electrode (GC) in CH3CN solutions, showing the quasi-reversible redox process ascribed to the reduction of the MII/MI couples. The X-ray single crystal structure data of the complex was matched excellently with the optimized monomer structure of the desired compound; Hirschfeld surface analysis supported the packed crystal lattice 3D network intermolecular forces. HOMO/LUMO energy level and the global reactivity descriptors quantum parameters are also calculated. The electrophilic and nucleophilic potions in the complex surface are theoretically evaluated by molecular electrostatic potential and Mulliken atomic charges analysis.

  19. 40 CFR 76.7 - Revised NOX emission limitations for Group 1, Phase II boilers.

    Science.gov (United States)

    2010-07-01

    ... Group 1, Phase II boilers. 76.7 Section 76.7 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... emission limitations for Group 1, Phase II boilers. (a) Beginning January 1, 2000, the owner or operator of a Group 1, Phase II coal-fired utility unit with a tangentially fired boiler or a dry bottom wall...

  20. Thermal Degradation Behaviour of Ni(II Complex of 3,4-Methylenedioxaphenylaminoglyoxime

    Directory of Open Access Journals (Sweden)

    Emin Karapınar

    2013-01-01

    Full Text Available Thermal degradation behaviour of the Ni(II complex of 3,4-methylenedioxaphenylaminoglyoxime was investigated by TG, DTA, and DTG at a heating rate of 10°C min−1 under dinitrogen. The acquired experimental data shows that the complex is thermally stable up to 541 K. The pyrolytic decomposition process occurs by melting metal complex and metal oxide remains as final product. The energies of the reactions involved and the mechanism of decomposition at each stage have been examined. The values of kinetic parameters such as activation energy (E, preexponential factor (A and thermodynamic parameters such as enthalpy (ΔH, entropy (ΔS, and Gibbs free energy (ΔG are also evaluated.

  1. Synthesis, experimental and theoretical characterizations of a new Schiff base derived from 2-pyridincarboxaldehyde and its Ni (II) complex

    Science.gov (United States)

    Habibi, Mohammad; Beyramabadi, S. Ali; Allameh, Sadegh; Khashi, Maryam; Morsali, Ali; Pordel, Mehdi; Khorsandi-Chenarboo, Mahdi

    2017-09-01

    In this work, a tridentate Schiff base of 2-pyridinecarboxaldehyde and its Ni(II) complex have been newly synthesized and characterized by the IR and NMR spectroscopies together with the elemental analysis. In addition, optimized geometries, the Natural Bond Orbital (NBO) analyses, assignment of the IR bands and NMR chemical shifts of the synthesized compounds were computed by using density functional theory (DFT) methods. In the optimized geometry of the free ligand, the aromatic rings are not in the same plane. But, the Ni complex is square planar, where the deprotonated Schiff base acts as a N3-tridentate ligand. The chloro ligand occupies another coordination position of the complex. The DFT-calculated vibrational wavenumbers and NMR chemical shifts are in agreement with the experimental values, confirming suitability of the optimized geometries for the Schiff base and Ni(II) complex.

  2. The MUSE Hubble Ultra Deep Field Survey. VII. Fe II* emission in star-forming galaxies

    Science.gov (United States)

    Finley, Hayley; Bouché, Nicolas; Contini, Thierry; Paalvast, Mieke; Boogaard, Leindert; Maseda, Michael; Bacon, Roland; Blaizot, Jérémy; Brinchmann, Jarle; Epinat, Benoît; Feltre, Anna; Marino, Raffaella Anna; Muzahid, Sowgat; Richard, Johan; Schaye, Joop; Verhamme, Anne; Weilbacher, Peter M.; Wisotzki, Lutz

    2017-11-01

    Non-resonant Fe II* (λ2365, λ2396, λ2612, λ2626) emission can potentially trace galactic winds in emission and provide useful constraints to wind models. From the 3.15' × 3.15' mosaic of the Hubble Ultra Deep Field (UDF) obtained with the VLT/MUSE integral field spectrograph, we identify a statistical sample of 40 Fe II* emitters and 50 MgIII (λλ2796,2803) emitters from a sample of 271 [O II]λλ3726,3729 emitters with reliable redshifts from z = 0.85-1.50 down to 2 × 10-18 (3σ) ergs s-1 cm-2 (for [O II]), covering the M⋆ range from 108-1011 M⊙. The Fe II* and Mg II emitters follow the galaxy main sequence, but with a clear dichotomy. Galaxies with masses below 109 M⊙ and star formation rates (SFRs) of ≲ 1 M⊙ yr-1 have MgIII emission without accompanying Fe II* emission, whereas galaxies with masses above 1010 M⊙ and SFRs ≳ 10 M⊙ yr-1 have Fe II* emission without accompanying MgIII emission. Between these two regimes, galaxies have both MgIII and Fe II* emission, typically with MgIII P Cygni profiles. Indeed, the MgIII profile shows a progression along the main sequence from pure emission to P Cygni profiles to strong absorption, due to resonant trapping. Combining the deep MUSE data with HST ancillary information, we find that galaxies with pure MgIII emission profiles have lower SFR surface densities than those with either MgIII P Cygni profiles or Fe II* emission. These spectral signatures produced through continuum scattering and fluorescence, MgIII P Cygni profiles and Fe II* emission, are better candidates for tracing galactic outflows than pure MgIII emission, which may originate from HIII regions. We compare the absorption and emission rest-frame equivalent widths for pairs of FeIII transitions to predictions from outflow models and find that the observations consistently have less total re-emission than absorption, suggesting either dust extinction or non-isotropic outflow geometries.

  3. Synthesis, Characterization, and Structural Assessment of Ni(II Complexes Derived from Bis(2-hydroxy-1-naphthaldehydesuccinoyldihydrazone

    Directory of Open Access Journals (Sweden)

    Mithun Chakrabarty

    2015-01-01

    Full Text Available The monometallic nickel(II complexes [Ni(H2nsh(A2]·nH2O (where A = water (H2O, n=0 (1; pyridine (py, n=2 (2; 2-picoline(2-pic, n=0 (3; 3-picoline(3-pic, n=2 (4; and 4-picoline(4-pic, n=0 (5 and homobimetallic nickel(II complexes [Ni2(nsh(A4]·nH2O (where A = water (H2O, n=1 (6; pyridine (py, n=4 (7; 2-picoline(2-pic, n=4 (8; 3-picoline(3-pic, n=4 (9; and 4-picoline(4-pic, n=4 (10, resp. have been synthesized in methanol from bis(2-hydroxy-1-naphthaldehydesuccinoyldihydrazone (H4nsh. The complexes have been characterized by elemental analyses, molar conductance, magnetic moment, and electronic and IR and TGA/DTA spectroscopic studies. The monometallic complexes (1 to (5 are found to have octahedral stereochemistry while complexes (6 to (10 are found to have distorted octahedral stereochemistry in which one of the Ni(II centres is present in N2O2 coordination sphere and another Ni(II centre is bonded to it through phenolate oxygen atoms via oxo-bridging.

  4. Electrochemical processing of WC-Ni pseudo alloys in sulfuric acid solutions to ammonium paratungstate and nickel(II) sulfate

    International Nuclear Information System (INIS)

    Kuntyj, O.I.; Ivashkiv, V.R.; Yavorskij, V.T.; Zozulya, G.I.

    2007-01-01

    Electrolysis of a WC-Ni pseudo alloy in aqueous sulfuric acid solutions was studied to develop a method for secondary tungsten waste utilization. A flowsheet for production of ammonium paratungstate and nickel(II) sulfate is suggested, in which the process solutions are recycled. The major electrolysis parameters are presented [ru

  5. Protein immobilization on Ni(II) ion patterns prepared by microcontact printing and dip-pen nanolithography

    NARCIS (Netherlands)

    Wu, Chien-Ching; Reinhoudt, David N; Otto, Cees; Velders, Aldrik H; Subramaniam, Vinod

    2010-01-01

    An indirect method of protein patterning by using Ni(II) ion templates for immobilization via a specific metal-protein interaction is described. A nitrilotriacetic acid (NTA)-terminated self-assembled monolayer (SAM) allows oriented binding of histidine-tagged proteins via complexation with late

  6. Extractive separation of Al(III) and Ni(II) by Di-2-Ethylhexyl phosphoric acid-kerosene system from aqueous fluoride medium

    International Nuclear Information System (INIS)

    Islam, M.F.; Begum, D.A.; Rahman, M.; Rahman, M.S.

    2009-01-01

    In the study of the extractive separation of Al(III) and Ni(II) by di-2-ethylhexyl phosphoric acid D2EHPA-kerosene from aqueous fluoride medium, about 94% Al(III) and 2% Ni(II) were extracted with 0.3 M D2EHPA (pH 2.1 and temperature 30+-1 degree C). Extraction of Ni(II) decreased with increasing extractant concentration. D2EHPA-kerosene-fluoride system showed better extraction of Al(III) with higher extractant concentration and aqueous pH and vice versa for the extraction of Ni(II). The maximum separation factor (beta 1380) was obtained for Al(III) at 20 degree C and decreased to (beta 732) at 60 degree C. The separation of Al(III) from Ni(II) was favoured at normal temperature. Extraction followed the order Al(III), Ni(II). About 99% stripping of Al(III) was attained from the loaded 0.20 M D2EHPA. Much faster extraction of Al(III) compared to Ni(II) and preferential loading were shown by D2EHPA-kerosene in the presence of fluoride ion in the aqueous phase. Separation of Al(III) was the most outstanding from Ni-Al-F-complex solution. (author)

  7. Thermolysis synthesis of pure phase NiO from novel sonochemical synthesized Ni(II) nano metal-organic supramolecular architecture.

    Science.gov (United States)

    Hanifehpour, Younes; Morsali, Ali; Mirtamizdoust, Babak; Joo, Sang Woo; Soltani, Behzad

    2017-07-01

    Nano-structures of a new supramolecular coordination compound of divalent nickel with the pyrazol (pzH) containing the terminal azide anions, [Ni(pzH) 2 (N 3 ) 2 ] (1), with discrete molecular architecture (DMA) in solid state was synthesized via sonochemical method. The new nanostructure was characterized by scanning electron microscopy, X-ray powder diffraction, IR, and elemental analysis. Compound 1 was structurally characterized by single crystal X-ray diffraction and the single-crystal X-ray data shows that the coordination number of Ni (II) ions is six, (NiN 6 ), with four N-donor atoms from neutral "pzH" ligands and two N-donors from two terminal azide anions. The supramolecular features in these complexes are guided and controlled by weak directional intermolecular interactions. The structure of the title complex was optimized by density functional theory calculations. Calculated structural parameters and IR spectra for the title complex are consistent with the crystal structure. The NiO nanoparticles were obtained by thermolysis of 1 at 180°C with oleic acid as a surfactant. Copyright © 2017 Elsevier B.V. All rights reserved.

  8. Synthesis, spectral, thermal and magnetic studies of Mn(II), Ni(II) and Cu(II) complexes with some benzopyran-4-one Schiff bases

    Science.gov (United States)

    El-Ansary, Aida L.; Abdel-Fattah, Hussein M.; Abdel-Kader, Nora S.

    2011-08-01

    The Schiff bases of N 2O 2 dibasic ligands, H 2La and H 2Lb are prepared by the condensation of ethylenediamine (a) and trimethylenediamine (b) with 6-formyl-7-hydroxy-5-methoxy-2-methylbenzopyran-4-one. Also tetra basic ligands, H 4La and H 4Lb are prepared by the condensation of aliphatic amines (a) and (b) with 6-formyl-5,7-dihydroxy-2-methylbenzopyran-4-one. New complexes of H 4La and H 4Lb with metal ions Mn(II), Ni(II) and Cu(II) are synthesized, in addition Mn(II) complexes with ligands H 2La and H 2Lb are also synthesized. Elemental and thermal analyses, infrared, ultraviolet-visible as well as conductivity and magnetic susceptibility measurements are used to elucidate the structure of the newly prepared metal complexes. The structures of copper(II) complexes are also assigned based upon ESR spectra study. All the complexes separated with the stoichiometric ratio (1:1) (M:L) except Mn-H 4La and Mn-H 4Lb with (2:1) (M:L) molar ratio. In metal chelates of the type 1:1 (M:L), the Schiff bases behave as a dinegative N 2O 2 tetradentate ligands. Moreover in 2:1 (M:L) complexes, the Schiff base molecules act as mono negative bidentate ligand and binuclear complex is then formed. The Schiff bases were assayed by the disc diffusion method for antibacterial activity against Staphylococcus aureus and Escherichia coli. The antifungal activity of the Schiff bases was also evaluated against the fungi Aspergillus flavus and Candida albicans.

  9. Effective removal of Ni(II) from aqueous solutions by modification of nano particles of clinoptilolite with dimethylglyoxime.

    Science.gov (United States)

    Nezamzadeh-Ejhieh, Alireza; Kabiri-Samani, Mehdi

    2013-09-15

    In this work an Iranian natural clinoptilolite tuff was pre-treated and changed to the micro (MCP) and nano (NCP) particles by mechanical method. Modification of micro and nano particles and also their Ni-exchanged forms were done by dimethylglyoxime (DMG). The raw and modified samples were characterized by XRD, FT-IR, SEM, BET, TG-DTG and energy dispersive analysis X-ray spectroscopy (EDAX). Removal of Ni(II) by modified and unmodified samples was investigated in batch procedure. It was found that NCP-DMG has higher capacity for removal of Ni(II). The effects of analytical parameters such as pH, dose of DMG, concentration of nickel solution, contact time and selectivity were studied and the optimal operation parameters were found as follows: pHPZC: 7.6, CNi(II): 0.01 M, contact time: 360 min and DMG dosage: 5mM. The results of selectivity experiments showed that the modified zeolite has a good selectivity for nickel in the presence of different multivalent cations. Langmuir and Freundlich isotherm models were adopted to describe the adsorption isotherms. Adsorption isotherms of Ni(II) ions could be best modelled by Langmuir equation, that indicate the monolayer sorption of Ni(II). Comparison of two kinetic models indicates that the adsorption kinetic can be well described by the pseudo-second-order rate equation that indicates that the rate limiting step for the process involves chemical reaction. The negative ΔH and ΔG indicate an exothermic and spontaneously process. The negative ΔS indicates that the adsorption of nickel cations from solution occurs with lower amount ion replacement, thus chemisorptions due to complex formation are dominant process in nickel removal. Copyright © 2013 Elsevier B.V. All rights reserved.

  10. 2-(hydroxymethyl)-1H-benzo[d]imidazole-5-carboxylic acid as linker for Co(II)/Ni(II)/Cu(II) coordination polymers: Synthesis, structures and properties

    Science.gov (United States)

    Wang, Duo-Zhi; Wang, Xin-Fang; Du, Jia-Qiang; Dong, Jun-Liang; Xie, Fei

    2018-02-01

    We report the synthesis and characterization of five transition metal coordination polymers (CPs) based on M(II) (M: Co, Ni and Cu), 2-(hydroxymethyl)-1H-benzo[d]imidazole-5-carboxylic acid (H2L) ligand. They are formulated as {[Co2(HL)2(H2O)3(SO4)]·H2O}n (1), {[Co2(HL)2(H2O)2]·SiF6}n (2), {[Ni2(HL)2(H2O)3(SO4)]·2H2O}n (3), {[Ni2(HL)2(H2O)4]·H2O·SiF6}n (4), {[Cu2(HL)2(H2O)2]·SiF6}n (5). The complexes 1-5 structure were characterized by single-crystal X-ray diffraction, elemental analyses, infrared spectroscopy (IR), powder X-ray diffraction (PXRD), and thermogravimetric analyses (TGA). Complexes 1-5 are two-dimensional (2D) network type coordination polymers that 1-3, 5 crystallize in monoclinic system within the centrosymmetric space group P2(1)/c, and 4 in triclinic system P-1 space group, they show the same coordination modes (κ1-κ1)-(κ1)-(κ1)-μ3 in coordination polymers. Complexes 1 and 3 expand to three-dimensional framework by means of hydrogen bond interactions, and can be rationalized to be three-connected {63} topological network, while 2, 4, 5 exhibit the topological network with a four-connected {44·62} topological sql network. The luminescent properties (for complexes 1, 2) and UV diffuse reflectance (for complexes 1-5) in the solid state at room temperature were also investigated and discussed. Complexes 1-5 act as effective heterogeneous catalysts, under mild conditions, for the homocoupling reaction of 4-substituted aryl iodides bearing electron-donating groups (-CH3, -OCH3).

  11. Synthesis and characterization of Cu(II), Co(II) and Ni(II) complexes of a number of sulfadrug azodyes and their application for wastewater treatment

    Science.gov (United States)

    El-Baradie, K.; El-Sharkawy, R.; El-Ghamry, H.; Sakai, K.

    2014-03-01

    The azodye ligand (HL1) was synthesized from the coupling of sulfaguanidine diazonium salt with 2,4-dihydroxy-benzaldehyde while the two ligands, HL2 and HL3, were prepared by the coupling of sulfadiazine diazonium salt with salicylaldehyde (HL2) and 2,4-dihydroxy-benzaldehyde (HL3). The prepared ligands were characterized by elemental analysis, IR, 1H NMR and mass spectra. Cu(II), Co(II) and Ni(II) complexes of the prepared ligands have been synthesized and characterized by various spectroscopic techniques like IR, UV-Visible as well as magnetic and thermal (TG and DTA) measurements. It was found that all the ligands behave as a monobasic bidentate which coordinated to the metal center through the azo nitrogen and α-hydroxy oxygen atoms in the case of HL1 and HL3. HL2 coordinated to the metal center through sulfonamide oxygen and pyrimidine nitrogen. The applications of the prepared complexes in the oxidative degradation of indigo carmine dye exhibited good catalytic activity in the presence of H2O2 as an oxidant. The reactions followed first-order kinetics and the rate constants were determined. The degradation reaction involved the catalytic action of the azo-dye complexes toward H2O2 decomposition, which can lead to the generation of HOrad radicals as a highly efficient oxidant attacking the target dye. The detailed kinetic studies and the mechanism of these catalytic reactions are under consideration in our group.

  12. Ni(II) complexes of arginine Schiff-bases and its interaction with DNA

    International Nuclear Information System (INIS)

    Sallam, S.A.; Abbas, A.M.

    2013-01-01

    Ni(II) complexes with Schiff-bases obtained by condensation of arginine with salicylaldehyde; 2,3-; 2,4-; 2,5-dihydroxybenzaldehyde and o-hydroxynaphthaldehyde have been synthesized using the template method in ethanol or ammonia media. They were characterized by elemental analyses, conductivity measurements, magnetic moment, UV, IR and 1 H NMR spectra as well as thermal analysis (TG, DTG and DTA). The Schiff-bases are dibasic tridentate donors and the complexes have diamagnetic square planar and octahedral structures. The complexes decompose in three steps where kinetic and thermodynamic parameters of the decomposition steps were computed. The interactions of the formed complexes with FM-DNA were monitored by UV and fluorescence spectroscopy. -- Highlights: ► Arginine Schiff-bases and their nickel(II) complexes have been synthesized. ► Magnetic and spectral data show diamagnetic square planar and octahedral complexes. ► The complexes thermally decompose in three stages. Interaction with FM-DNA shows hyperchromism with blue shift

  13. Tetracarboxylate-based Co(II), Ni(II) and Cu(II) three-dimensional coordination polymers: syntheses, structures and magnetic properties.

    Science.gov (United States)

    Su, Shengqun; Guo, Zhiyong; Li, Guanghua; Deng, Ruiping; Song, Shuyan; Qin, Chao; Pan, Chengling; Guo, Huadong; Cao, Feng; Wang, Song; Zhang, Hongjie

    2010-10-14

    Methylenediisophthalic acid (H(4)MDIP), as semi-rigid 'V'-shaped carboxylate ligands, react with CoO, NiO and Cu(NO(3))(2)·3H(2)O to give three novel coordination polymers [H(3)O](2)[Co(3)(MDIP)(2)]·2DMF (1), [Ni(2)(HMDIP)(μ(2)-OH)(H(2)O)(3)(DMF)]·4H(2)O·DMF (2) and [Cu(3)(MDIP)(μ(2)-OH)(2)(H(2)O)(4)]·6.5H(2)O (3) (DMF = N,N'-dimethylformamide). All compounds have been characterized by thermogravimetric analysis, IR spectroscopy, elemental and single-crystal X-ray diffraction analyses. Complex 1 is an unusual open anionic framework that is defined as the metal-organic replica of fluorite. Both 2 and 3 features a 3D open framework with one-dimensional elliptical channels and R- and L-helical chains, and their resulting frameworks can be rationalized as crb and pts topology respectively. An interesting feature of complex 3 is the presence of the linear Cu(3) units that is formed by carboxylate and μ(2)-hydroxyl groups linking three Cu(II) metal centers. Magnetic investigations indicate that ferromagnetic couplings are dominant in the three compounds.

  14. Involvement of organic acids and amino acids in ameliorating Ni(II) toxicity induced cell cycle dysregulation in Caulobacter crescentus: a metabolomics analysis.

    Science.gov (United States)

    Jain, Abhishek; Chen, Wei Ning

    2018-04-03

    Nickel (Ni(II)) toxicity is addressed by many different bacteria, but bacterial responses to nickel stress are still unclear. Therefore, we studied the effect of Ni(II) toxicity on cell proliferation of α-proteobacterium Caulobacter crescentus. Next, we showed the mechanism that allows C. crescentus to survive in Ni(II) stress condition. Our results revealed that the growth of C. crescentus is severely affected when the bacterium was exposed to different Ni(II) concentrations, 0.003 mM slightly affected the growth, 0.008 mM reduced the growth by 50%, and growth was completely inhibited at 0.015 mM. It was further shown that Ni(II) toxicity induced mislocalization of major regulatory proteins such as MipZ, FtsZ, ParB, and MreB, resulting in dysregulation of the cell cycle. GC-MS metabolomics analysis of Ni(II) stressed C. crescentus showed an increased level of nine important metabolites including TCA cycle intermediates and amino acids. This indicates that changes in central carbon metabolism and nitrogen metabolism are linked with the disruption of cell division process. Addition of malic acid, citric acid, alanine, proline, and glutamine to 0.015 mM Ni(II)-treated C. crescentus restored its growth. Thus, the present work shows a protective effect of these organic acids and amino acids on Ni(II) toxicity. Metabolic stimulation through the PutA/GlnA pathway, accelerated degradation of CtrA, and Ni-chelation by organic acids or amino acids are some of the possible mechanisms suggested to be involved in enhancing C. crescentus's tolerance. Our results shed light on the mechanism of increased Ni(II) tolerance in C. crescentus which may be useful in bioremediation strategies and synthetic biology applications such as the development of whole cell biosensor.

  15. Application of Zr/Ti-Pic in the adsorption process of Cu(II), Co(II) and Ni(II) using adsorption physico-chemical models and thermodynamics of the process; Aplicacao de Zr/Ti-PILC no processo de adsorcao de Cu(II), Co(II) e Ni(II) utilizando modelos fisico-quimicos de adsorcao e termodinamica do processo

    Energy Technology Data Exchange (ETDEWEB)

    Guerra, Denis Lima; Airoldi, Claudio [Universidade Estadual de Campinas (UNICAMP), SP (Brazil). Inst. de Quimica. Dept. de Quimica Inorganica]. E-mail: dlguerra@iqm.unicamp.br; Lemos, Vanda Porpino; Angelica, Romulo Simoes [Universidade Federal do Para (UFPa), Belem (Brazil); Viana, Rubia Ribeiro [Universidade Federal do Mato Grosso (UFMT), Cuiaba (Brazil). Inst. de Ciencias Exatas e da Terra. Dept. de Recursos Minerais

    2008-07-01

    The aim of this investigation is to study how Zr/Ti-Pic adsorbs metals. The physico-chemical proprieties of Zr/Ti-Pic have been optimized with pillarization processes and Cu(II), Ni(II) and Co(II) adsorption from aqueous solution has been carried out, with maximum adsorption values of 8.85, 8.30 and 7.78 x-1 mmol g{sup -1}, respectively. The Langmuir, Freundlich and Temkin adsorption isotherm models have been applied to fit the experimental data with a linear regression process. The energetic effect caused by metal interaction was determined through calorimetric titration at the solid-liquid interface and gave a net thermal effect that enabled the calculation of the exothermic values and the equilibrium constant. (author)

  16. THE CONNECTIONS BETWEEN THE UV AND OPTICAL Fe ii EMISSION LINES IN TYPE 1 AGNs

    Energy Technology Data Exchange (ETDEWEB)

    Kovacević-Dojcinović, Jelena; Popović, Luka Č., E-mail: jkovacevic@aob.bg.ac.rs, E-mail: lpopovic@aob.bg.ac.rs [Astronomical Observatory, Volgina 7, 11060 Belgrade (Serbia)

    2015-12-15

    We investigate the spectral properties of the UV (λλ2650–3050 Å) and optical (λλ4000–5500 Å) Fe ii emission features in a sample of 293 Type 1 active galactic nuclei (AGNs) from the Sloan Digital Sky Survey database. We explore different correlations between their emission line properties, as well as the correlations with other emission lines from the spectral range. We find several interesting correlations and outline the most interesting results as follows. (i) There is a kinematical connection between the UV and optical Fe ii lines, indicating that the UV and optical Fe ii lines originate from the outer part of the broad line region, the so-called intermediate line region. (ii) The unexplained anticorrelations of the optical Fe ii equivalent width (EW Fe ii{sub opt}) versus EW [O iii] 5007 Å and EW Fe ii{sub opt} versus FWHM Hβ have not been detected for the UV Fe ii lines. (iii) The significant averaged redshift in the UV Fe ii lines, which is not present in optical Fe ii, indicates an inflow in the UV Fe ii emitting clouds, and probably their asymmetric distribution. (iv) Also, we confirm the anticorrelation between the intensity ratio of the optical and UV Fe ii lines and the FWHM of Hβ, and we find the anticorrelations of this ratio with the widths of Mg ii 2800 Å, optical Fe ii, and UV Fe ii. This indicates a very important role for the column density and microturbulence in the emitting gas. We discuss the starburst activity in high-density regions of young AGNs as a possible explanation of the detected optical Fe ii correlations and intensity line ratios of the UV and optical Fe ii lines.

  17. Tuning avalanche criticality: acoustic emission during the martensitic transformation of a compressed Ni-Mn-Ga single crystal

    Czech Academy of Sciences Publication Activity Database

    Niemann, R.; Baró, J.; Heczko, Oleg; Schultz, L.; Fähler, S.; Vives, E.; Mañosa, L.; Planes, A.

    2012-01-01

    Roč. 86, č. 21 (2012), "214101-1"-"214101-6" ISSN 1098-0121 R&D Projects: GA ČR(CZ) GAP107/11/0391 Institutional research plan: CEZ:AV0Z10100520 Keywords : stress -induced martensitic transformation * Ni-Mn-Ga * magnetic shape memory alloy * ferromagnetic martensite * acoustic emission during transformation Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 3.767, year: 2012

  18. Faint emission features in the Mg II resonance-line wings. [in solar spectra

    Science.gov (United States)

    Allen, M. S.; Mcallister, H. C.

    1977-01-01

    Data obtained with a rocket-borne echelle spectrograph are presented which indicate the presence of three faint emission features deep in the cores of the Mg II h and k resonance-line wings in the solar Fraunhofer spectrum. Results of wavelength measurements are discussed, and the relative intensities of the emission features are examined. It is tentatively suggested that the first feature be identified with the Fe II line at 2797.037 A, the second feature is probably the V II line at 2803.469 A, and the third feature may originate in Fe II emission at 2804.021 A. Possible emission mechanisms are proposed, and it is concluded that the detected features may be of potential diagnostic value for the analysis of depth variations of temperature and velocity in the lower chromosphere as well as for solar and possibly stellar spectroscopy.

  19. Variability of fire carbon emissions in equatorial Asia and its nonlinear sensitivity to El Niño

    Science.gov (United States)

    Yin, Yi; Ciais, Philippe; Chevallier, Frederic; Werf, Guido R.; Fanin, Thierry; Broquet, Gregoire; Boesch, Hartmut; Cozic, Anne; Hauglustaine, Didier; Szopa, Sophie; Wang, Yilong

    2016-10-01

    The large peatland carbon stocks in the land use change-affected areas of equatorial Asia are vulnerable to fire. Combining satellite observations of active fire, burned area, and atmospheric concentrations of combustion tracers with a Bayesian inversion, we estimated the amount and variability of fire carbon emissions in equatorial Asia over the period 1997-2015. Emissions in 2015 were of 0.51 ± 0.17 Pg carbon—less than half of the emissions from the previous 1997 extreme El Niño, explained by a less acute water deficit. Fire severity could be empirically hindcasted from the cumulative water deficit with a lead time of 1 to 2 months. Based on CMIP5 climate projections and an exponential empirical relationship found between fire carbon emissions and water deficit, we infer a total fire carbon loss ranging from 12 to 25 Pg by 2100 which is a significant positive feedback to climate warming.

  20. Biosorption Study of Ni(II on Apple Peel Granola from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Mohammad Hossien Salmani Nodoushan

    2014-11-01

    Full Text Available Introduction: Nickel is found in varies industrial processes such as electroplating, leather tanning, cement preservations, paints and pigments, textile, steel fabrication and canning industries. It is proved that Ni(II has several health hazards such as carcinogenic. The aim of this study was the evaluation of Ni(IIadsorption on Apple peel granola from aqueous solution. Material and Methods: This study was done in laboratory scale and batch condition. In this study, the effects adsorbent dose, contact time and pH were investigated on the removal of nickel by batch process. The Apple peels granola prepared in lab conditions, and sieved by standard sieves of 60-100 mesh. The nickel concentration in standard and unknown samples was measured by AA spectrophotometer. For understanding of the adsorption process, the experimental data were analyzed with some isotherm and kinetic models. Results: The maximum removal at was found in pH= 7. The nickel removal efficiency decreased from 50.1 to 25% by increasing adsorbent dosage. By increasing of pH from 3 to 7, the removal efficiency increased from 19.8% to 35.0% at 30 min contact time. The adsorption isotherm and Kinetic analysis of our results showed that the results well fitted by the Frundlich isotherm model (R2= 0.909 and pseudo-first-order kinetic model (R2= 0.926. Conclusion: the results showed that Apple peel granola is able to absorb the nickel from aqueous solutions and removal efficiency was more in pH=7. Preparing of Apple peel granola adsorbent is simple, cheap and its application is in priority because of its porous structure in comparison with other natural adsorbents.

  1. Pre-equilibrium emission and nuclear level densities in neutron induced reactions on Fe, Cr and Ni isotopes

    International Nuclear Information System (INIS)

    Ivascu, M.; Avrigeanu, M.; Ivascu, I.; Avrigeanu, V.

    1989-01-01

    The experimentally well known (n,p), (n,α) and (n,2n) reaction excitation functions, from threshold to 20 MeV incident energy, and neutron, proton and alpha-particle emission spectra at 14.8 MeV from Fe, Cr and Ni isotopes are calculated in the frame of a generalized Geometry-Dependent-Hybrid pre-equilibrium emission model, including angular momentum and parity conservation and alpha-particle emission, and the Hauser-Feshbach statistical model. Use of a consistent statistical model parameter set enables the validation of the pre-equilibrium emission model. Moreover, an enhanced pre-equilibrium emission from higher spin composite system states, associated with higher incident orbital momenta, has been evidenced. Higher orbital momenta involved also in the emergent channels of this process are suggested by calculations of the residual nuclei level populations. Finally, the unitary account of the (n, p) and (n, 2n) reaction excitation functions for Fe, Cr and Ni isotopes has allowed the proper establishment of the limits of the transition excitation range between the two different nuclear level density models used at medium and higher excitation energies, respectively. (author). 83 refs, 15 figs

  2. DNA incision evaluation, binding investigation and biocidal screening of Cu(II), Ni(II) and Co(II) complexes with isoxazole Schiff bases.

    Science.gov (United States)

    Ganji, Nirmala; Chityala, Vijay Kumar; Marri, Pradeep Kumar; Aveli, Rambabu; Narendrula, Vamsikrishna; Daravath, Sreenu; Shivaraj

    2017-10-01

    Two new series of binary metal complexes [M(L 1 ) 2 ] and [M(L 2 ) 2 ] where, M=Cu(II), Ni(II) & Co(II) and L 1 =4-((3,4-dimethylisoxazol-5-ylimino)methyl)benzene-1,3-diol; L 2 =2-((3,4-dimethylisoxazol-5-ylimino)methyl)-5-methoxyphenol were synthesized and characterized by elemental analysis, 1 H NMR, 13 C NMR, FT-IR, ESI mass, UV-Visible, magnetic moment, ESR, SEM and powder XRD studies. Based on these results, a square planar geometry is assigned for all the metal complexes where the Schiff base acts as uninegatively charged bidentate chelating agent via the hydroxyl oxygen and azomethine nitrogen atoms. DNA binding studies of all the complexes with calf thymus DNA have been comprehensively investigated using electronic absorption spectroscopy, fluorescence quenching and viscosity studies. The oxidative and photo cleavage affinity of metal complexes towards supercoiled pBR322 DNA has been ascertained by agarose gel electrophoresis assay. From the results, it is observed that all the metal complexes bind effectively to CT-DNA via an intercalative mode of binding and also cleave pBR322 DNA in a promising manner. Further the Cu(II) complexes have shown better binding and cleavage properties towards DNA. The antimicrobial activities of the Schiff bases and their metal complexes were studied on bacterial and fungal strains and the results denoted that the complexes are more potent than their Schiff base ligands. Copyright © 2017 Elsevier B.V. All rights reserved.

  3. Copolymerization of ethylene with polar monomers: chain propagation and side reactions. A DFT theoretical study using zwitterionic Ni(II) and Pd(II) catalysts.

    Science.gov (United States)

    Szabo, Miklos J; Galea, Natasha M; Michalak, Artur; Yang, Sheng-Yong; Groux, Laurent F; Piers, Warren E; Ziegler, Tom

    2005-10-26

    Calculations utilizing anionic substituted derivates of the cationic N(wedge)N--Ni(II) and Pd(II) diimine Brookhart complex have been carried out on the barriers of ethylene and acrylonitrile insertion into a M- methyl, propyl and CH(CN)Et bond for M = Ni, Pd. The possibility of side reactions such as chelate formation with the polar functionality and oligomerization of the active species after acrylonitrile insertion are explored. The diimine ring system N--N = -NR' 'CR(1)CR(2)NR' ' with R' ' = 2,6-C(6)H(3)(i-Pr)(2) and R(1),R(2) = Me was functionalized by adding one or two anionic groups (BF(3)(-), etc.) in place of i-Pr on the aryl rings or by replacing one Me diimine backbone group (R(1)) with BH(3)(-). The objective of this investigation is computationally to design catalysts for ethylene/acrylonitrile copolymerization that have activities that are comparable to that of the cationic Ni(II) diimine or at least the Pd(II) diimine Brookhart system for ethylene homopolymerization. Complexes that might meet this objective are discussed.

  4. Two interpenetrating Cu{sup II}/Ni{sup II}-coordinated polymers based on an unsymmetrical bifunctional N/O-tectonic: Syntheses, structures and magnetic properties

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Yong-Liang [College of Materials & Chemical Engineering, China Three Gorges University, Yichang 443002 (China); Department of Chemistry and Chemical Engineering, Shaanxi Key Laboratory of Comprehensive Utilization of Tailings Resources, Shang Luo University, Shang Luo 726000 (China); Wu, Ya-Pan [College of Materials & Chemical Engineering, China Three Gorges University, Yichang 443002 (China); Li, Dong-Sheng, E-mail: lidongsheng1@126.com [College of Materials & Chemical Engineering, China Three Gorges University, Yichang 443002 (China); Dong, Wen-Wen [College of Materials & Chemical Engineering, China Three Gorges University, Yichang 443002 (China); Zhou, Chun-Sheng [Department of Chemistry and Chemical Engineering, Shaanxi Key Laboratory of Comprehensive Utilization of Tailings Resources, Shang Luo University, Shang Luo 726000 (China)

    2015-03-15

    Two new interpenetrating Cu{sup II}/Ni{sup II} coordination polymers, based on a unsymmetrical bifunctional N/O-tectonic 3-(pyrid-4′-yl)-5-(4″-carbonylphenyl)-1,2,4-triazolyl (H{sub 2}pycz), ([Cu-(Hpycz){sub 2}]·2H{sub 2}O){sub n} (1) and ([Ni(Hpycz){sub 2}]·H{sub 2}O){sub n} (2), have been solvothermally synthesized and structure characterization. Single crystal X-ray analysis indicates that compound 1 shows 2-fold parallel interpenetrated 4{sup 4}-sql layers with the same handedness. The overall structure of 1 is achiral—in each layer of doubly interpenetrating nets, the two individual nets have the opposite handedness to the corresponding nets in the adjoining layers—while 2 features a rare 8-fold interpenetrating 6{sup 6}-dia network that belongs to class IIIa interpenetration. In addition, compounds 1 and 2 both show similar paramagnetic characteristic properties. - Graphical abstract: Two new Cu(II)/Ni(II) coordination polymers present 2D parallel 2-fold interpenetrated 4{sup 4}-sql layers and a rare 3D 8-fold interpenetrating 6{sup 6}-dia network. In addition, magnetic susceptibility measurements show similar paramagnetic characteristic for two complexes. - Highlights: • A new unsymmetrical bifunctional N/O-tectonic as 4-connected spacer. • A 2-fold parallel interpenetrated sql layer with the same handedness. • A rare 8-fold interpenetrating dia network (class IIIa)

  5. Syntheses, spectroscopic and thermal analyses of the hofmann-type metal(II tetra- cyanonickelate(II pyridazine complexes: {[M(pdzNi(CN4]∙H2O}n (M = Zn(II or Cd(II

    Directory of Open Access Journals (Sweden)

    D. Karaağaç

    2015-10-01

    Full Text Available Two new Hofmann-type complexes in the form of {[M(pdzNi(CN4]·H2O}n [where pdz = pyridazine; M = Zn(II and M = Cd(II] have been synthesized as a powder and their structural properties have been characterized by vibrational (FT-IR and Raman spectroscopy, thermal and elemental analysis. The spectral and thermal analysis results suggest that these complexes are similar in structure to the Hofmann type complexes and their structures consist of polymeric layers of │M−Ni(CN4│∞ with the pdz bound to the metal (M atom. DOI: http://dx.doi.org/10.4314/bcse.v29i3.9

  6. Bis(diphenylphosphino)methane-phosphonate ligands and their Pd(II), Ni(II) and Cu(I) complexes. Catalytic oligomerization of ethylene.

    Science.gov (United States)

    Hamada, Adel; Braunstein, Pierre

    2009-02-16

    The bis(diphenylphosphino)methane-phosphonate-based (dppm-phosphonate) ligands (Ph(2)P)(2)CHP(O)(OR)(2) (R = Me, L(1); R = Ph, L(2)) form metal complexes by selective coordination of the diphosphine moiety to Pd(II) and Ni(II) centers. The formation of complexes containing the chelating, deprotonated form of ligand L(1) or L(2) occurred when basic ligands were present in the precursor complex, such as Me or dmba (on Pd(II)) or acac (on Ni(II)). The Cu(I) complex [CuL(1)](2)(BF(4))(2) (9) was obtained that is suggested to be dinuclear, each Cu(I) being chelated by a phosphine and a P=O donor and further bound to the phosphine group of another ligand. The crystal structures of the mononuclear complexes [PdCl(2){(Ph(2)P)(2)CHP(O)(OMe)(2)-P,P}] (2a), [PdCl(2){(Ph(2)P)(2)CHP(O)(OPh)(2)-P,P}] (2b), [Pd{(Ph(2)P)(2)CP(O)(OMe)(2)-P,P}(2)] (6a) in 6a.2CH(2)Cl(2), [Pd{(Ph(2)P)(2)CP(O)(OPh)(2)-P,P}(2)] (6b), [Ni{(Ph(2)P)(2)CP(O)(OMe)(2)-P,P}(2)] (10a) in 10a.4CHCl(3), [Ni{(Ph(2)P)(2)CP(O)(OPh)(2)-P,P}(2)] (10b) in 10b.4CHCl(3), [NiCl(2){(Ph(2)P)(2)CHP(O)(OMe)(2)-P,P}] (11a) in 11a.CHCl(3) and of the dinuclear complexes [Pd(mu-Cl){(Ph(2)P)(2)CP(O)(OMe)(2)-P,P}](2) (7a) and [Pd(mu-Cl){(Ph(2)P)(2)CP(O)(OPh)(2)-P,P}](2) (7b) have been determined by X-ray diffraction. The complexes [Ni{(Ph(2)P)(2)CC(O)NPh(2)-P,P}(2)] (13) and [Ni{Ph(2)PC(Ph)P(O)(OEt)(2)-P,O}(2)] (15) were prepared by reaction of [Ni(acac)(2)] with the known, neutral ligands (Ph(2)P)(2)CHC(O)NPh(2) and Ph(2)PCH(Ph)P(O)(OEt)(2), respectively. The Ni(II) complexes were evaluated for the catalytic oligomerization of ethylene and afforded similar results when AlEtCl(2) was used as cocatalyst. Complexes 11a,b were the most active, with a turnover frequency (TOF) of 78 300 mol of C(2)H(4)/(mol of Ni)h) for complex 11b in the presence of 10 equiv of AlEtCl(2) and showed a high selectivity for C(4) and C(6) olefins with up to 93% C(4) for 10a in the presence of 6 equiv AlEtCl(2), whereas when only 3 equiv cocatalyst was

  7. Synthesis, characterization and physicochemical studies of new chelating resin 1, 8-(3, 6-dithiaoctyl)-4-polyvinylbenzenesulphonate (dpvbs) and its metallopolymer Cu(II), Ni(II), Co(II) and Fe(III) complexes

    Science.gov (United States)

    Khalil, Tarek E.; Elbadawy, Hemmat A.; El-Dissouky, Ali

    2018-02-01

    A new chelating resin, 1,8-(3,6-dithiaoctyl)-4-polyvinylbenzenesulphonate (dpvbs) has been synthesized by coupling Amberlite XAD-16 with (2,2‧-ethylenedithio) diethanol using pyridine/CH2Cl2 mixture as a solvent. The chelating resin and its metallopolymer Cu(II), Ni(II), Co(II) and Fe(III) complexes have been synthesized and characterized by EDS, SEM, XPS, elemental analysis, spectral (IR, UV/Vis, EPR). The thermal analysis of the resin and its metallopolymer complexes indicated an endothermic spontaneous sorption mechanism with the liberation of water of hydration of the metal ions and that adsorbed by the free resin. At the solid liquid interface, the degrees of freedom increased during the sorption of the metal ions onto the resin. The surface area of polymer support and its metallopolymer complexes are estimated by (BJH) method. The batch equilibrium method was used for studying the metal sorption and selectivity at different pH values and different contact times at room temperature. ICP-AES was used to estimate the metal capacity of the resin for sorption of Cu(II), Ni(II), Co(II) and Fe(III) from aqueous solutions utilizing the batch equilibrium method. The sorption tendency of the metal ions by the resin was found to be: Cu(II) > Fe(III) > Co(II) > Ni(II). Adsorption kinetics was found to be fit the pseudo-second order model.

  8. Power train and emission control: allocation procedure by OBD-II system for automotive technology

    Science.gov (United States)

    Kalita, Porag

    2017-06-01

    OBD-II, systems were designed to maintain low emissions of in use vehicles, including light and medium duty vehicles. In 1989, the California code of Regulations (CCR) known as OBD - II was adopted by the California Air Resource Board (CARB) and the objective to reduce hydrocarbon (HC) emission caused by malfunction of the vehicles emission control systems. OBD-II provides additional information to engineer for diagnosis and repair of emissions related problems. OBD-II, standardizes on the amount of memory (Freeze Frame) it uses to store the readings of the vehicle sensor when it logs on emission related Intermittent Trouble code (IT). The intent of OBD-II, systems is to detect most vehicle malfunctions when performance of a power train component or system deteriorates to the point that the vehicle’s HC emission exceed standard. The vehicle operator is notified at the time when the vehicle begins to marginally exceed emission standards, by illuminating the Malfunctions Indicator Light (MIL).

  9. Synthesis, spectroscopic characterization, DNA interaction and biological activities of Mn(II), Co(II), Ni(II) and Cu(II) complexes with [(1H-1,2,4-triazole-3-ylimino)methyl]naphthalene-2-ol

    Science.gov (United States)

    Gaber, Mohamed; El-Wakiel, Nadia A.; El-Ghamry, Hoda; Fathalla, Shaimaa K.

    2014-11-01

    Manganese(II), cobalt(II), nickel(II) and copper(II) complexes of [(1H-1,2,4-triazole-3-ylimino)methyl]naphthalene-2-ol have been synthesized. The structure of complexes have been characterized by elemental analysis, molar conductance, magnetic moment measurements and spectral (IR, 1H NMR, EI-mass, UV-Vis and ESR), and thermal studies. The results showed that the chloro and nitrato Cu(II) complexes have octahedral geometry while Ni(II), Co(II) and Mn(II) complexes in addition to acetato Cu(II) complex have tetrahedral geometry. The possible structures of the metal complexes have been computed using the molecular mechanic calculations using the hyper chem. 8.03 molecular modeling program to confirm the proposed structures. The kinetic and thermodynamic parameters of the thermal decomposition steps were calculated from the TG curves. The binding modes of the complexes with DNA have been investigated by UV-Vis absorption titration. The results showed that the mode of binding of the complexes to DNA is intercalative or non-intercalative binding modes. Schiff base and its metal complexes have been screened for their in vitro antimicrobial activities against Gram positive bacteria (Staphylococcus aureus), Gram negative bacteria (Escherichia coli and Pesudomonas aeruginosa), fungi (Asperigllus flavus and Mucer) and yeast (Candida albicans and Malassezia furfur).

  10. Transparent nanostructured electrodes: Electrospun NiO nanofibers/NiO films

    Energy Technology Data Exchange (ETDEWEB)

    Lamastra, F.R. [Italian Interuniversity Consortium on Materials Science and Technology (INSTM), Research Unit Roma Tor Vergata, Via del Politecnico 1, 00133 Rome (Italy); Nanni, F. [Italian Interuniversity Consortium on Materials Science and Technology (INSTM), Research Unit Roma Tor Vergata, Via del Politecnico 1, 00133 Rome (Italy); Department of Enterprise Engineering, University of Rome Tor Vergata, Via del Politecnico 1, 00133 Rome (Italy); Menchini, F. [ENEA, CR Casaccia, Via Anguillarese 301, 00123 Rome (Italy); Nunziante, P. [Italian Interuniversity Consortium on Materials Science and Technology (INSTM), Research Unit Roma Tor Vergata, Via del Politecnico 1, 00133 Rome (Italy); Department of Chemical Sciences and Technologies, University of Rome Tor Vergata, Via della Ricerca Scientifica 1, 00133 Rome (Italy); Grilli, M.L., E-mail: marialuisa.grilli@enea.it [ENEA, CR Casaccia, Via Anguillarese 301, 00123 Rome (Italy)

    2016-02-29

    Polyvinylpyrrolidone (PVP)/nickel(II) acetate precursor fibers were deposited by electrospinning directly on radio frequency sputtered thin Ni and NiO films grown on quartz substrate, starting from Ni(II) acetate and PVP solution in ethanol. The samples were calcined in air in the temperature range 400–500 °C to obtain transparent and conductive p-type NiO nanofibers on NiO films. A higher density of nanofibers was obtained on Ni/quartz substrates, as compared to NiO/quartz ones, demonstrating the feasibility of fiber adhesion directly to an insulating substrate previously coated by a thin Ni layer. Samples were characterized by field emission-scanning electron microscopy, X-ray diffraction, spectrophotometric and resistance measurements. - Highlights: • Nanostructured electrodes: electrospun NiO nanofibers/NiO films were fabricated. • NiO fibers were directly grown on insulating substrate coated by thin Ni or NiO films. • Good quality crystalline fibers were obtained at low calcination temperatures. • Transparent and conductive p-type electrodes were fabricated.

  11. Quest II: reduction of co2 emissions of reefer containers

    NARCIS (Netherlands)

    Lukasse, L.J.S.; Baerentz, M.B.; Kramer, de J.E.

    2013-01-01

    This paper reports on the QuestTM II (QUality and Energy in Storage and Transport) development project run by Wageningen UR Food & Biobased Research, Maersk Line and Carrier Transicold. The aim of the Quest II development project was to improve the control of refrigerated marine container

  12. Estudo da estabilidade do complexo ácido fítico e o íon Ni(II Study of stability of phytic acid with Ni(II complex

    Directory of Open Access Journals (Sweden)

    Ligia De Carli

    2006-03-01

    Full Text Available A técnica de titulação potenciométrica foi utilizada para verificar as propriedades ácida-base do ácido fítico [1,2,3,4,5,6-hexaquis(dihidrogenofosfato-mio-inositol] e do complexo ácido fítico e Ni(II, em solução aquosa, em temperatura e força iônica constantes. Para avaliar o comportamento térmico e a complexação do ácido fítico com o íon Ni(II foram realizadas análises de Termogravimetria (TG, Termogravimetria Derivada (DTG, Calorimetria Exploratória Diferencial (DSC e estudos de Espectrofotometria de Infravermelho. Foram obtidas oito constantes de protonação da amostra de ácido fítico na forma de sal de dipotássio e sete constantes de estabilidade do complexo ácido fítico e Ni(II. As reações de protonação e de formação ocorrem na faixa de pH de 2,0 a 11,0. Os dados obtidos mostram que o ácido fítico encontra-se totalmente deprotonado em pH 12,0 no qual a espécie ML (um ligante para um íon metálico encontra-se totalmente formada no mesmo valor de pH. Os resultados obtidos por TG e DSC revelaram tanto para o ácido fítico como para o complexo boa estabilidade até a temperatura próxima a 200ºC. Por TG, DTG e DSC conclui-se também que a estequiometria do complexo estudado foi de um mol de ligante para um mol de íon metálico. A Espectrofotometria de Infravermelho comprovou a estabilidade do ácido fítico e a sua interação com o íon Ni(II.The technique of potenciometric titration was used to verify the acid-basic properties of the phytic acid, [1,2,3,4,5,6-hexakis(dihydrogen phosphate-myo-inositol] and the Phytic Acid-Ni(II complex, in aqueous solution, in constant temperature and ionic strength. To evaluate the thermal behavior end complexation of the isolated phytic acid with the Ni(II were performed analyses of thermogravimetry (TG, calorimetric scanning differential (DSC and studies Spectroscopy Infrared (IR. Eight protonation constants of the phytic acid sample as dipotassium salt were

  13. The Origins of [C II] Emission in Local Star-forming Galaxies

    NARCIS (Netherlands)

    Croxall, K. V.; Smith, J. D T; Pellegrini, E.; Groves, Brent; Bolatto, Alberto; Herrera-Camus, Rodrigo; Sandstrom, K. M.; Draine, Bruce; Wolfire, M. G.; Armus, Lee; Boquien, Mederic; Brandl, B.R.; Dale, Daniel A.; Galametz, Maud; Hunt, L. K.; Kennicutt, R. C.; Kreckel, K.; Rigopoulou, D.; van der werf, p; Wilson, C

    2017-01-01

    The [C ii] 158 μm fine-structure line is the brightest emission line observed in local star-forming galaxies. As a major coolant of the gas-phase interstellar medium, [C ii] balances the heating, including that due to far-ultraviolet photons, which heat the gas via the photoelectric effect.

  14. Characterization of Toxicologically Relevant Compounds From Diesel Emissions: Phase II

    National Research Council Canada - National Science Library

    Yost, Douglas M; Schulman, Matthew E; Frame, Edwin A

    2004-01-01

    A light-duty diesel engine fitted with a common-rail fuel injection system was calibrated on several alternative type test fuels to achieve low engine-out oxides of nitrogen (NOx) exhaust emissions...

  15. Modified Acoustic Emission for Prognostic Health Monitoring, Phase II

    Data.gov (United States)

    National Aeronautics and Space Administration — Prime Photonics proposes to team with Dr. Duke of Virginia Tech to develop a multi-mode, enhanced piezoelectric acoustic emission sensing system to couple large...

  16. Synthesis, characterization, DFT and biological studies of (Z)-N‧-(2-oxoindolin-3-ylidene)picolinohydrazide and its Co(II), Ni(II) and Cu(II) complexes

    Science.gov (United States)

    Rakha, T. H.; El-Gammal, O. A.; Metwally, H. M.; Abu El-Reash, G. M.

    2014-03-01

    The picolinohydrazide derivative: (Z)-N‧-(2-oxoindolin-3-ylidene)picolinohydrazide (H2IPH) and its Co(II), Ni(II) and Cu(II) complexes have been synthesized and investigated by using the modern spectroscopic and physicochemical techniques viz. IR, 1H NMR, UV-Vis spectrometric methods and magnetic moment measurements. The investigation study revealed that the ligand acts as monobasic tri- and tetradentate in Co(II) and Ni(II) complex, respectively and as neutral tridentate in Cu(II) complex. On the basis of magnetic moment and spectral studies, a six coordinated octahedral geometry is assigned for all complexes. The molecular modeling are drawn and showed the bond length, bond angle, chemical reactivity, energy components (kcal/mol) and binding energy (kcal/mol) for all the title compounds and also NLO for the ligand is shown. The energy gap between the HOMO and LUMO for Ni(II) complex is (-7 eV) which indicates that these compound is a promising structure for photovoltaic devices such as solar cells. A comparison of the experimental and theoretical spectra can be very useful in making correct assignments and understanding the basic chemical shift. The thermal behavior and the kinetic parameters of degradation were determined using Coats-Redfern and Horowitz-Metzger methods. The in vitro antibacterial studies of these complexes screened against pathogenic bacteria proved them as growth inhibiting agents. Antitumor activity, carried out in vitro on human mammary gland (breast) MCF7, have shown that the Co(II) complex exhibited potent activity followed by the ligand, Cu(II) and Ni(II) complexes.

  17. Synthesis, Spectral, Magnetic and Thermal Studies of the Complexes of CoII and NiII With Some Bidentate and Tridentate Hydrazone Ligands

    Directory of Open Access Journals (Sweden)

    Chetan K. Modi

    2005-01-01

    Full Text Available The reaction of Co(NO32.6H2O and Ni(NO32.6H2O with hydrazones derived from 1-phenyl-3-methyl-4-acyl-5-pyrazolone (where acyl = acetyl, propionyl, butyryl and benzoyl with 2-picolinic acid hydrazide have been studied and characterized on the basis of elemental analysis, magnetic moments, molar conductivity measurements, IR and electronic spectral studies and thermogravimetric analysis. Various ligand field parameters have been calculated. Electronic spectral data and the magnetic moment values suggest an octahedral structure for all cobalt(II and nickel(II complexes.

  18. Structure of the Ni(II) complex of Escherichia coli peptide deformylase and suggestions on deformylase activities depending on different metal(II) centres.

    Science.gov (United States)

    Yen, Ngo Thi Hai; Bogdanović, Xenia; Palm, Gottfried J; Kühl, Olaf; Hinrichs, Winfried

    2010-02-01

    Crystal structures of polypeptide deformylase (PDF) of Escherichia coli with nickel(II) replacing the native iron(II) have been solved with chloride and formate as metal ligands. The chloro complex is a model for the correct protonation state of the hydrolytic hydroxo ligand and the protonated status of the Glu133 side chain as part of the hydrolytic mechanism. The ambiguity that recently some PDFs have been identified with Zn(2+) ion as the active-site centre whereas others are only active with Fe(2+) (or Co(2+), Ni(2+) is discussed with respect to Lewis acid criteria of the metal ion and substrate activation by the CD loop.

  19. Evaluation of the Marine Algae Gracilaria and its Activated Carbon for the Adsorption of Ni(II from Wastewater

    Directory of Open Access Journals (Sweden)

    A. Esmaeili

    2011-01-01

    Full Text Available The batch removal of Ni2+ from aqueous solution and wastewater using marine dried (MD red algae Gracilaria and its activated carbon (AC was studied. For these experiments, adsorption of Ni2+ was used to form two biomasses of AC and MD. Both methods used different pH values, biomass and initial concentration of Ni2+. Subsequently adsorption models and kinetic studies were carried out. The maximum efficiencies of Ni2+ removal were 83.55% and 99.04% for MD and AC respectively developed from it. The experimental adsorption data were fitted to the Langmuir adsorption model. The nickel(II uptake by the biosorbents was best described by pseudo-second order rate model. The kinetic studies showed that the heavy metal uptake was observed more rapidly by the AC with compared to MD. AC method developed from MD biomass exhibited higher biosorption capacity. Adsorption capacity is related to the pH of solution, pH 5.0 is optimal for nickel. The maximum efficiencies of Ni2+ removal were for AC method. The capacity is related to the pH of solution, pH 5.0 is optimal for nickel. The equilibrium adsorption data are correlated by Langmuir isotherm equation. The adsorption kinetic data can be described by the second order kinetic models

  20. Field emission properties and strong localization effect in conduction mechanism of nanostructured perovskite LaNiO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Kamble, Ramesh B., E-mail: rbk.physics@coep.ac.in [Department of Physics, Indian Institute of Science, Bangalore 560012, Karnataka (India); Department of Physics, College of Engineering, Pune 411005, Maharashtra (India); Tanty, Narendra; Patra, Ananya; Prasad, V. [Department of Physics, Indian Institute of Science, Bangalore 560012, Karnataka (India)

    2016-08-22

    We report the potential field emission of highly conducting metallic perovskite lanthanum nickelate (LaNiO{sub 3}) from the nanostructured pyramidal and whisker shaped tips as electron emitters. Nano particles of lanthanum nickelate (LNO) were prepared by sol-gel route. Structural and morphological studies have been carried out. Field emission of LNO exhibited high emission current density, J = 3.37 mA/cm{sup 2} at a low threshold electric field, E{sub th} = 16.91 V/μm, obeying Fowler–Nordheim tunneling. The DC electrical resistivity exhibited upturn at 11.6 K indicating localization of electron at low temperature. Magnetoresistance measurement at different temperatures confirmed strong localization in nanostructured LNO obeying Anderson localization effect at low temperature.

  1. Ultrasonically assisted solvothermal synthesis of novel Ni/Al layered double hydroxide for capturing of Cd(II) from contaminated water

    Science.gov (United States)

    Rahmanian, Omid; Maleki, Mohammad Hassan; Dinari, Mohammad

    2017-11-01

    A novel adsorbent of nickel aluminum layered double hydroxide (Ni/Al-LDH) was prepared through the precipitation of metal nitrates by ultrasonically assisted solvothermal method. The surface morphology, chemical structure and thermal properties of this compound were examined by X-ray diffraction (XRD), Fourier Transform Infrared (FT-IR), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), and thermogravimetric analysis (TGA) techniques. The XRD, TEM and FE-SEM results established that the synthesized LDH have a well-ordered layer structure with good crystalline nature. Then it was applied to remove excessive Cd(II) ions from water and the effects of contact time, pH and adsorbent dose were examined at initial Cd(II) concentration of 10 mg/L. Results show that the time required to reach equilibrium was fast (40 min) and working pH solution was neutral (pH 7). Langmuir and Freundlich model of adsorption isotherms were explored; the results show that the Freundlich model was better fitted than that Langmuir model. This results predicting a multilayer adsorption of Cd(II) on LDH. The equilibrium kinetic adsorption data were fixed to the pseudo-second order kinetic equation.

  2. Rapid removal of Ni(II from aqueous solution using 3-Mercaptopropionic acid functionalized bio magnetite nanoparticles

    Directory of Open Access Journals (Sweden)

    Sada Venkateswarlu

    2015-12-01

    Full Text Available The surfaces of bio magnetite nanoparticles were functionalized with 3-Mercaptopropionic acid (3 MPA and used as a high-capacity and recyclable adsorbent for the rapid removal of Ni(II from aqueous solution. The 3 MPA@Fe3O4 MNPs were characterized by Fourier transformed infrared analysis (FT-IR, transmission electron microscopy (TEM, energy dispersive X-ray spectroscopy (EDS and vibrating sample magnetometer (VSM analysis. This 3 MPA@Fe3O4 MNPs have been used for removal of Ni(II from aqueous solution. The hysteresis loops of 3 MPA@Fe3O4 MNPs shows an excellent ferromagnetic behavior with saturation magnetization value of 14.02 emu/g. The adsorption isotherm data were fitted well to Langmuir isotherm, the monolayer adsorption capacity was found to be 42.01 mg/g at 303 K. The experimental kinetic data fitted very well the pseudo-second-order model.The results indicate that the biogenic 3 MPA@Fe3O4 MNPs act as significant adsorbent material for removal of Ni(II aqueous solution and also considered as a potential adsorbent for hazardous metal ions from wastewater.

  3. Equilibrium, kinetic and thermodynamic studies for sorption of Ni (II from aqueous solution using formaldehyde treated waste tea leaves

    Directory of Open Access Journals (Sweden)

    Jasmin Shah

    2015-05-01

    Full Text Available The sorption characteristic of Ni (II from aqueous solution using formaldehyde treated waste tea leaves as a low cost sorbent has been studied. The effect of pH, contact time, sorbent dose, initial metal ion concentration and temperature were investigated in batch experiments. The equilibrium data were fitted into four most common isotherm models; Freundlich, Langmuir, Tempkin and Dubinin–Radushkevich (D–R. The Langmuir model described the sorption isotherm best with maximum monolayer sorption capacity of 120.50 mg g−1. Four kinetic models, pseudo-first-order, pseudo-second-order, intraparticle diffusion and Elovich were employed to explain the sorption mechanism. The kinetics of sorption data showed that the pseudo-second-order model is the best with correlation coefficient of 0.9946. The spontaneous and exothermic nature of the sorption process was revealed from thermodynamic investigations. The effect of some common alkali and alkaline earth metal ions were also studied which showed that the presence of these ions have no effect on the sorption of Ni (II. The results showed that waste tea leaves have the potential to be used as a low cost sorbent for the removal of Ni (II from aqueous solutions.

  4. Synthesis, spectroscopic characterization, DFT calculations and biological evaluation of benzothiazole derivative bearing Mn(II) and Ni(II) metal ions

    Science.gov (United States)

    El-Gamel, Nadia E. A.; Ali, Korany A.

    2017-11-01

    N-(benzo[d]thiazol-2-yl)-3-oxo-3-phenylpropanamide ligand and its Nickel and Manganese complexes have been synthesized and characterized by elemental and thermal analyses, IR, diffuse reflectance, mass and UV-Vis spectra, molar conductance and magnetic moment measurements. The decomposition mechanism and thermal stability of the investigated complexes are interpreted in terms of their structures. The thermal behaviour of the complexes has been studied and different thermodynamic parameters are calculated using Coats-Redfern method. N-(benzo[d]thiazol-2-yl)-3-oxo-3-phenylpropanamide is a neutral bidentate ligand coordinating metal ions via thiazole ring nitrogen and amide carbonyl O forming high spin octahedral complexes with Mn(II) (2) and distorted square planar in case of Ni(II) (1). Natural bond orbital analysis and geometry optimization were carried out at DFT/B3LYP/6-31G(d) level of theory for the ligand and the mentioned complexes. Ab inito computations at the HF/6-31G(d) level of the theory is conducted in order to detect any probability of a hydrogen bond formation in the ligand. The dipole moment of the Ni(II) and Mn(II) complexes is recorded to be 9.69 and 7.39 Debye, respectively, indicating that the complexes are more polarized than the ligand 2.39 Debye. The in vitro biological activity of the metal chelates is screened against the Gram-positive bacteria (Staphylococcus aureus) and Gram-negative bacteria (Escherichia coli), fungus (Aspergillus flavus, Candida albicans). Ni(II) complexes displayed the highest activity against Candida albicans and Staphylococcus aureus with MIC values of 13, 30 μg/cm3, respectively.

  5. Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases. Part 3: Michael addition reactions and miscellaneous transformations.

    Science.gov (United States)

    Aceña, José Luis; Sorochinsky, Alexander E; Soloshonok, Vadim

    2014-09-01

    The major goal of this review is a critical discussion of the literature data on asymmetric synthesis of α-amino acids via Michael addition reactions involving Ni(II)-complexes of amino acids. The material covered is divided into two conceptually different groups dealing with applications of: (a) Ni(II)-complexes of glycine as C-nucleophiles and (b) Ni(II)-complexes of dehydroalanine as Michael acceptors. The first group is significantly larger and consequently subdivided into four chapters based on the source of stereocontrolling element. Thus, a chiral auxiliary can be used as a part of nucleophilic glycine Ni(II) complex, Michael acceptor or both, leading to the conditions of matching vs. mismatching stereochemical preferences. The particular focus of the review is made on the practical aspects of the methodology under discussion and mechanistic considerations.

  6. NO EVIDENCE FOR A SYSTEMATIC Fe II EMISSION LINE REDSHIFT IN TYPE 1 ACTIVE GALACTIC NUCLEI

    International Nuclear Information System (INIS)

    Sulentic, Jack W.; Marziani, Paola; Zamfir, Sebastian; Meadows, Zachary A.

    2012-01-01

    We test the recent claim by Hu et al. that Fe II emission in type 1 active galactic nuclei shows a systematic redshift relative to the local source rest frame and broad-line Hβ. We compile high signal-to-noise median composites using Sloan Digital Sky Survey spectra from both the Hu et al. sample and our own sample of the 469 brightest DR5 spectra. Our composites are generated in bins of FWHM Hβ and Fe II strength as defined in our 4D Eigenvector 1 formalism. We find no evidence for a systematic Fe II redshift and consistency with previous assumptions that Fe II shift and width (FWHM) follow Hβ shift and FWHM in virtually all sources. This result is consistent with the hypothesis that Fe II emission (quasi-ubiquitous in type 1 sources) arises from a broad-line region with geometry and kinematics the same as that producing the Balmer lines.

  7. GALACTIC CEPHEIDS WITH SPITZER. II. SEARCH FOR EXTENDED INFRARED EMISSION

    International Nuclear Information System (INIS)

    Barmby, P.; Marengo, M.; Evans, N. R.; Huelsman, D.; Fazio, G. G.; Bono, G.; Su, K. Y. L.; Welch, D. L.

    2011-01-01

    A deep and detailed examination of 29 classical Cepheids with the Spitzer Space Telescope has revealed three stars with strong nearby extended emission detected in multiple bands which appears to be physically associated with the stars. RS Pup was already known to possess extended infrared emission, while the extended emission around the other two stars (S Mus and δ Cep) is newly discovered in our observations. Four other stars (GH Lup, l Car, T Mon, and X Cyg) show tentative evidence for extended infrared emission. An unusual elongated extended object next to SZ Tau appears to be a background or foreground object in a chance alignment with the Cepheid. The inferred mass-loss rate upper limits for S Mus and δ Cep are in the range from 10 -9 to 10 -8 M sun yr -1 , with the upper limit for RS Pup as high as 10 -6 M sun yr -1 . Mass loss during post-main-sequence evolution has been proposed as a resolution to the discrepancy between pulsational and dynamical masses of Cepheid variable stars: dust in the lost material would make itself known by the presence of an infrared bright nebula or unresolved infrared excess. The observed frequency of infrared circumstellar emission (<24%) and the mass-loss rate we estimate for our sources show that dusty mass loss can only account for part of the Cepheid mass-loss discrepancy. Nevertheless, our direct evidence that mass loss is active during the Cepheid phase is an important confirmation that these processes need to be included in evolutionary and pulsation models of these stars and should be taken into account in the calibration of the Cepheid distance scale.

  8. Sorption of Ni(II) on GMZ bentonite: effects of pH, ionic strength, foreign ions, humic acid and temperature.

    Science.gov (United States)

    Yang, Shitong; Li, Jiaxing; Lu, Yi; Chen, Yixue; Wang, Xiangke

    2009-09-01

    Bentonite has been widely studied in nuclear waste management because of its special physicochemical properties. In this work, the sorption of Ni(II) from aqueous solution onto GMZ bentonite as a function of contact time, pH, ionic strength, foreign ions, humic acid (HA) and temperature was investigated under ambient conditions. The results indicated that the pseudo-second-order rate equation simulated the kinetic sorption process well. The sorption of Ni(II) on GMZ bentonite was strongly dependent on pH and on ionic strength. At low pH, the sorption of Ni(II) was dominated by outer-sphere surface complexation and ion exchange with Na(+)/H(+) on GMZ bentonite surfaces, whereas inner-sphere surface complexation was the main sorption mechanism at high pH. A positive effect of HA on Ni(II) sorption was found at pH8. The Langmuir, Freundlich, and D-R models were used to simulate the sorption isotherms of Ni(II) at three different temperatures: 303.15, 318.15 and 333.15K. The thermodynamic parameters (DeltaH(0), DeltaS(0) and DeltaG(0)) of Ni(II) sorption on GMZ bentonite at the three different temperatures were calculated from the temperature-dependent sorption isotherms. The results indicated that the sorption process of Ni(II) on GMZ bentonite was endothermic and spontaneous. Experimental results indicate that GMZ bentonite is a suitable sorbent for pre-concentration and solidification of Ni(II) from large volume solutions.

  9. Sorption of Ni(II) on GMZ bentonite: Effects of pH, ionic strength, foreign ions, humic acid and temperature

    International Nuclear Information System (INIS)

    Yang Shitong; Li Jiaxing; Lu Yi; Chen Yixue; Wang Xiangke

    2009-01-01

    Bentonite has been widely studied in nuclear waste management because of its special physicochemical properties. In this work, the sorption of Ni(II) from aqueous solution onto GMZ bentonite as a function of contact time, pH, ionic strength, foreign ions, humic acid (HA) and temperature was investigated under ambient conditions. The results indicated that the pseudo-second-order rate equation simulated the kinetic sorption process well. The sorption of Ni(II) on GMZ bentonite was strongly dependent on pH and on ionic strength. At low pH, the sorption of Ni(II) was dominated by outer-sphere surface complexation and ion exchange with Na + /H + on GMZ bentonite surfaces, whereas inner-sphere surface complexation was the main sorption mechanism at high pH. A positive effect of HA on Ni(II) sorption was found at pH 8. The Langmuir, Freundlich, and D-R models were used to simulate the sorption isotherms of Ni(II) at three different temperatures: 303.15, 318.15 and 333.15 K. The thermodynamic parameters (ΔH 0 , ΔS 0 and ΔG 0 ) of Ni(II) sorption on GMZ bentonite at the three different temperatures were calculated from the temperature-dependent sorption isotherms. The results indicated that the sorption process of Ni(II) on GMZ bentonite was endothermic and spontaneous. Experimental results indicate that GMZ bentonite is a suitable sorbent for pre-concentration and solidification of Ni(II) from large volume solutions.

  10. Adsorption phenomena of cubane-type tetranuclear Ni(II) complexes with neutral, thioether-functionalized ligands on Au(111)

    Science.gov (United States)

    Heß, Volkmar; Matthes, Frank; Bürgler, Daniel E.; Monakhov, Kirill Yu.; Besson, Claire; Kögerler, Paul; Ghisolfi, Alessio; Braunstein, Pierre; Schneider, Claus M.

    2015-11-01

    The controlled and intact deposition of molecules with specific properties onto surfaces is an emergent field impacting a wide range of applications including catalysis, molecular electronics, and quantum information processing. One strategy is to introduce grafting groups functionalized to anchor to a specific surface. While thiols and disulfides have proven to be quite effective in combination with gold surfaces, other S-containing groups have received much less attention. Here, we investigate the surface anchoring and organizing capabilities of novel charge-neutral heterocyclic thioether groups as ligands of polynuclear nickel(II) complexes. We report on the deposition of a cubane-type {Ni4} (= [Ni(μ3-Cl)Cl(HL·S)]4) single-molecule magnet from dichloromethane solution on a Au(111) surface, investigated by scanning tunneling microscopy, X-ray photoelectron spectroscopy, and low-energy electron diffraction, both immediately after deposition and after subsequent post-annealing. The results provide strong evidence for partial decomposition of the coordination complex upon deposition on the Au(111) surface that, however, leaves the magnetic {Ni4Cl4n} (n = 1 or 2) core intact. Only post-annealing above 480 K induces further decomposition and fragmentation of the {Ni4Cl4n} core. The detailed insight into the chemisorption-induced decomposition pathway not only provides guidelines for the deposition of thioether-functionalized Ni(II) complexes on metallic surfaces but also reveals opportunities to use multidentate organic ligands decorated with thioether groups as transporters for highly unstable inorganic structures onto conducting surfaces, where they are stabilized retaining appealing electronic and magnetic properties.

  11. Sampling for Air Chemical Emissions from the Life Sciences Laboratory II

    Energy Technology Data Exchange (ETDEWEB)

    Ballinger, Marcel Y. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Lindberg, Michael J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2017-03-30

    Sampling for air chemical emissions from the Life Science Laboratory II (LSL-II) ventilation stack was performed in an effort to determine potential exposure of maintenance staff to laboratory exhaust on the building roof. The concern about worker exposure was raised in December 2015 and several activities were performed to assist in estimating exposure concentrations. Data quality objectives were developed to determine the need for and scope and parameters of a sampling campaign to measure chemical emissions from research and development activities to the outside air. The activities provided data on temporal variation of air chemical concentrations and a basis for evaluating calculated emissions. Sampling for air chemical emissions was performed in the LSL-II ventilation stack over the 6-week period from July 26 to September 1, 2016. A total of 12 sampling events were carried out using 16 sample media. Resulting analysis provided concentration data on 49 analytes. All results were below occupational exposure limits and most results were below detection limits. When compared to calculated emissions, only 5 of the 49 chemicals had measured concentrations greater than predicted. This sampling effort will inform other study components to develop a more complete picture of a worker’s potential exposure from LSL-II rooftop activities. Mixing studies were conducted to inform spatial variation in concentrations at other rooftop locations and can be used in conjunction with these results to provide temporal variations in concentrations for estimating the potential exposure to workers working in and around the LSL-II stack.

  12. Synthesis, characterization and DNA cleavage studies of isomeric pyridyl-tetrazole ligands and their Ni(II and Zn(II complexes

    Directory of Open Access Journals (Sweden)

    M.S. Surendra Babu

    2017-03-01

    Full Text Available A new series of Ni(II and Zn(II complexes were synthesized from bidentate isomeric pyridyl tetrazole ligands such as 2-(1-vinyl-1H-tetrazol-5-ylpyridine (L1, N,N-dimethyl-3-(5-(pyridin-2-yl-1H-tetrazol-1-ylpropan-1-amine(L2, 2-(2-vinyl-2H-tetrazol-5-ylpyridine(L3, N,N-dimethyl-3-(5-(pyridin-2-yl-2H-tetrazol-2-ylpropan-1-amine (L4. All the complexes were characterized by the elemental analysis, molar conductance, FTIR, UV–vis and magnetic studies. The conductance and spectroscopic data suggested that, the ligands act as monobasic bidentate ligands and form octahedral complexes with general formula [M(L1−42Cl2], (M = Ni(II and Zn(II. In addition metal complexes displayed good antioxidant and moderate nematicidal activities. The cytotoxicity of ligands and their metal complexes have been evaluated by MTT assay. The DNA cleavage activity of the metal complexes was performed using agarose gel electrophoresis in the presence and absence of oxidant H2O2. All metal complexes showed significant nuclease activity in the presence of H2O2.

  13. Studies on some VO(IV, Ni(II and Cu(II complexes of non-symmetrical tetradentate Schiff-bases

    Directory of Open Access Journals (Sweden)

    Aderoju A. Osowole

    2008-08-01

    Full Text Available The coordination chemistry of VO(IV, Ni(II and Cu(II with unsymmetrical Schiff base ligands, [HO(OCH3C6H3C(CH3:N(CH2CH2N:C(CH3CH:C(C6H5OH], H2L and [HO(OCH3C6H3C(CH3:N(CH2CH2N:C(CH3CH:C(CH3OH], H2L1 (derived from condensation of 1-phenyl-1,3-butanedione/2,4-pentanedione, ethylenediamine and 5-methoxy-2-hydroxy acetophenone is discussed. The metal complexes were characterized by elemental analysis, molar conductance, magnetic susceptibility, infrared and electronic spectral measurements. They are magnetically dilute, non-electrolytes in nitromethane. The ligands are tetradentately coordinating via the imine N and enolic O atoms, resulting in 5-coordinate square-pyramidal geometry for the VO(IV complexes and 4-coordinate square-planar geometry for the Ni(II and Cu(II complexes. The assignment of geometry is supported by magnetic and spectral measurements.

  14. 2,4-Dinitrophenylhydrazine functionalized sodium dodecyl sulfate-coated magnetite nanoparticles for effective removal of Cd(II) and Ni(II) ions from water samples.

    Science.gov (United States)

    Sobhanardakani, Soheil; Zandipak, Raziyeh

    2015-07-01

    2,4-Dinitrophenylhydrazine immobilized on sodium dodecyl sulfate (SDS)-coated magnetite and was used for removal of Cd(II) and Ni(II) ions from aqueous solution. The prepared product was characterized by X-ray diffraction (XRD) analysis, Fourier transform infrared spectroscopy (FT-IR), and scanning electron microscopy (SEM). The size of the nanoparticles according to SEM was obtained around 20-35 nm. In batch tests, the effects of pH, contact time, initial metal concentration, and temperature were studied. The kinetic and equilibrium data were modeled with recently developed models. The adsorption kinetics and isotherms were well fitted by the fractal-like pseudo-second-order model and Langmuir-Freundlich model, respectively. Maximum adsorption capacity by this adsorbent is 255.1 mg g(-1) for Cd(II) ion and 319.6 mg g(-1) for Ni(II) ion at pH 7.0 and 25 °C. The method was successfully applied to the removal of metal cations in real samples (tap water, river water, and petrochemical wastewater).

  15. Elaboration of modified poly(NiII-DHS films as electrodes by the electropolymerization of Ni(II-[5,5′-dihydroxysalen] onto indium tin oxide surface and study of their electrocatalytic behavior toward aliphatic alcohols

    Directory of Open Access Journals (Sweden)

    Ali Ourari

    2017-11-01

    Full Text Available Nickel(II-DHS complex was obtained from N,N′-bis(2,5-dihydroxybenzylidene-1,2-diaminoethane (H2DHS ligand and nickel acetate tetrahydrated in ethanolic solution with stirring under reflux. This complex, dissolved in an alkaline solution, was oxidized to form electroactive films strongly adhered on the ITO (indium tin oxide electrode surface. In this alkaline solution, the poly-[NiII-DHS]/ITO films showed the typical voltammetric response of (Ni2+/Ni3+ redox couple centers which are immobilized in the polymer-film. The modified electrodes (MEs obtained were also characterized by several techniques such as scanning electronic microscopy, atomic force microscopy and electrochemical methods. The electrocatalytic behavior of these MEs toward the oxidation reaction of some aliphatic alcohols such as methanol, ethanol, 2-Methyl-1-propanol and isopropanol was investigated. The voltammograms recorded with these alcohols showed good electrocatalytic efficiency. The electrocatalytic currents were at least 80 times higher than those obtained for the oxidation of methanol on electrodes modified with nickel hydroxide films in alkaline solutions. We noticed that these electrocatalytic currents are proportional to the concentration of methanol (0.050–0.30 μM. In contrast, those recorded for the oxidation of other aliphatic short chain alcohols such as ethanol, 2-methyl-1-propanol and isopropanol are rather moderately weaker. In all cases the electrocatalytic currents presented a linear dependence with the concentration of alcohol. These modified electrodes could be applied as alcohol sensors.

  16. THE Fe II EMISSION IN ACTIVE GALACTIC NUCLEI: EXCITATION MECHANISMS AND LOCATION OF THE EMITTING REGION

    Energy Technology Data Exchange (ETDEWEB)

    Marinello, M. [Universidade Federal de Itajubá, Rua Doutor Pereira Cabral 1303, 37500-903, Itajubá, MG (Brazil); Rodríguez-Ardila, A.; Garcia-Rissmann, A. [Laboratório Nacional de Astrofísica, Rua Estados Unidos 154, Itajubá, MG, 37504-364 (Brazil); Sigut, T. A. A. [The University of Western Ontario, London, ON N6A 3K7 (Canada); Pradhan, A. K., E-mail: murilo.marinello@gmail.com [McPherson Laboratory, The Ohio State University, 140 W. 18th Ave., Columbus, OH 43210-1173 (United States)

    2016-04-01

    We present a study of Fe ii emission in the near-infrared region (NIR) for 25 active galactic nuclei (AGNs) to obtain information about the excitation mechanisms that power it and the location where it is formed. We employ an NIR Fe ii template derived in the literature and find that it successfully reproduces the observed Fe ii spectrum. The Fe ii bump at 9200 Å detected in all objects studied confirms that Lyα fluorescence is always present in AGNs. The correlation found between the flux of the 9200 Å bump, the 1 μm lines, and the optical Fe ii implies that Lyα fluorescence plays an important role in Fe ii production. We determined that at least 18% of the optical Fe ii is due to this process, while collisional excitation dominates the production of the observed Fe ii. The line profiles of Fe ii λ10502, O i λ11287, Ca ii λ8664, and Paβ were compared to gather information about the most likely location where they are emitted. We found that Fe ii, O i and Ca ii have similar widths and are, on average, 30% narrower than Paβ. Assuming that the clouds emitting the lines are virialized, we show that the Fe ii is emitted in a region twice as far from the central source than Paβ. The distance, though, strongly varies: from 8.5 light-days for NGC 4051 to 198.2 light-days for Mrk 509. Our results reinforce the importance of the Fe ii in the NIR to constrain critical parameters that drive its physics and the underlying AGN kinematics, as well as more accurate models aimed at reproducing this complex emission.

  17. Synthesis and vibrational spectroscopic characterisation of nickel (II) propionate tetrahydrate, Ni(CH 3CH 2COO) 2·4H 2O, and its aqueous solution

    Science.gov (United States)

    Bickley, R. I.; Edwards, H. G. M.; Gustar, R.; Rose, S. J.

    1991-08-01

    A two-stage synthesis for nickel(II) propionate is described. A comprehensive Raman and infrared spectroscopic study of propionic acid, nickel propionate, sodium propionate and barium propionate has been made and the vibrational spectra have been assigned. From comparisons of the Raman and infrared spectra of sodium propionate and nickel propionate, it is concluded that nickel (II) propionate dissociates into the propionate ion CH 3CH 2CO 2-, hexa-aquo nickel(II) ions Ni(H 2O) 2+6, and the monopropionato-nickel(II) species (CH 3CH 2COO)Ni +, in aqueous solution.

  18. Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases; Part 1: alkyl halide alkylations.

    Science.gov (United States)

    Sorochinsky, Alexander E; Aceña, José Luis; Moriwaki, Hiroki; Sato, Tatsunori; Soloshonok, Vadim A

    2013-10-01

    Alkylations of chiral or achiral Ni(II) complexes of glycine Schiff bases constitute a landmark in the development of practical methodology for asymmetric synthesis of α-amino acids. Straightforward, easy preparation as well as high reactivity of these Ni(II) complexes render them ready available and inexpensive glycine equivalents for preparing a wide variety of α-amino acids, in particular on a relatively large scale. In the case of Ni(II) complexes containing benzylproline moiety as a chiral auxiliary, their alkylation proceeds with high thermodynamically controlled diastereoselectivity. Similar type of Ni(II) complexes derived from alanine can also be used for alkylation providing convenient access to quaternary, α,α-disubstituted α-amino acids. Achiral type of Ni(II) complexes can be prepared from picolinic acid or via recently developed modular approach using simple secondary or primary amines. These Ni(II) complexes can be easily mono/bis-alkylated under homogeneous or phase-transfer catalysis conditions. Origin of diastereo-/enantioselectivity in the alkylations reactions, aspects of practicality, generality and limitations of this methodology is critically discussed.

  19. Preparation and estimation of thermodynamic properties of Fe(II)-, Co(II)-, Ni(II)- and Zr(IV)-containing layered double hydroxides

    Energy Technology Data Exchange (ETDEWEB)

    Rozov, Konstantin; Curtius, Hilde; Bosbach, Dirk [Forschungszentrum Juelich GmbH (Germany). Inst. for Nuclear Waste Management and Reactor Safety (IEK-6)

    2015-07-01

    The investigation of layered double hydroxides (LDHs) was performed because they and similar 'green rust' phases were identified as specific secondary phases forming during the evolution of the disposed research reactor fuel elements under nuclear repository relevant conditions. LDHs or 'hydrotalcite-like' solids are of interest in environmental geochemistry because they can substitute various cations and especially due to the anion-exchange properties and, therefore, can be considered as buffer materials for retention of mobile and hazardous radionuclides (like, {sup 14}C, {sup 129}I, {sup 36}Cl, {sup 79}Se etc.). In our study Fe{sup 2+}-, Co{sup 2+}-, Ni{sup 2+}- and Zr{sup 4+}-containing LDHs have been synthesized by co-precipitation method and characterized (PXRD, FT-IR, SEM-EDX, TGA-DSC) in order to investigate the effect of substitution of 2- and 4-valent cations on the stability of LDHs. PXRD measurements demonstrated that: (1) pure Mg-Al-Fe(II) LDHs are existing in the range of the mole fraction of iron x{sub Fe} = Fe/(Mg+Fe) between 0 and 0.13. Unit-cell parameters (a{sub o}=b{sub o}) as a function of x{sub Fe} follow Vegard's law corroborating the existence of a solid solution when x{sub Fe} = 0 - 0.13. Products of syntheses with x{sub Fe} ≥ 0.13 contain detectable amounts (≥1-2 wt%) of additional phases (like, magnetite, maghemite, lepidocrocite); (2) pure Ni{sup 2+}- and Co{sup 2+}-containing LDHs (mole fractions of Ni and Co were equal to 0.1) have been synthesized successfully; (3) Mg-Al-Zr(IV) precipitates with mole fraction of zirconium x{sub Zr} = Zr/(Zr+Al) = 0.0 - 0.5 show PXRD patterns attributed to pure LDHs and the variation of lattice parameters a{sub o}=b{sub o} as a function of x{sub Zr} is in agreement with Vegard's law demonstrating the presence of solid solution. In contrast, PXRD analyses of precipitates with x{sub Zr} ≥ 0.5 have shown the presence of additional X-ray reflexes typical for brucite. The

  20. Zn(II), Ni(II), Cu(II) and Pb(II) complexes of tridentate asymmetrical Schiff base ligands: Synthesis, characterization, properties and biological activity

    Science.gov (United States)

    Şahin, Mustafa; Koçak, Nuriye; Erdenay, Damla; Arslan, Uğur

    2013-02-01

    New asymmetrical tridentate Schiff base ligands were synthesized using 1,2-phenylenediamine, 4-methyl-1,2-phenylenediamine, 2-hydroxy-1-napthaldehyde, 9-anthracenecarboxaldehyde. Schiff base ligands and their metal complexes were synthesised and characterized by using FT-IR, 1H NMR, 13C NMR, UV-Vis, XRD, ESR, elemental analysis and fluorescence studies. The antimicrobial activity of the ligands and their metal complexes were studied against Staphylococcus aureus ATCC 29213, S. aureus ATCC 25923, Streptococcus mutans RSHM 676, Enterococcus faecalis ATCC 29212, Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853. The determination of the antibacterial activity was done using the broth microdilution methods. In general, it has been determined that the studied compounds have MIC values similar to Gram-positive and Gram-negative bacteria. It has been found that Ni, Pb, Zn derivatives of HL1A and ZnL2A has lower MIC values than ampicillin for P. aeruginosa ATCC 27853 strain.

  1. Mathematical modeling of Fe(II), Cu(II), Ni(II) and Zn(II) removal in a horizontal rotating tubular bioreactor.

    Science.gov (United States)

    Rezić, Tonči; Zeiner, Michaela; Santek, Božidar; Novak, Srđan

    2011-11-01

    Industrial wastewaters polluted with toxic heavy metals are serious ecological and environmental problem. Therefore, in this study multi-heavy metals (Fe(2+), Cu(2+), Ni(2+) and Zn(2+)) removal process with mixed microbial culture was examined in the horizontal rotating tubular bioreactor (HRTB) by different combinations of process parameters. Hydrodynamic conditions and biomass sorption capacity have main impact on the removal efficiency of heavy metals: Fe(2+) 95.5-79.0%, Ni(2+) 92.7-54.8%, Cu(2+) 87.7-54.9% and Zn(2+) 81.8-38.1%, respectively. On the basis of experimental results, integral mathematical model of removal heavy metals in the HRTB was established. It combines hydrodynamics (mixing), mass transfer and kinetics to define bioprocess conduction in the HRTB. Mixing in the HRTB was described by structured cascade model and metal ion removal by two combined diffusion-adsorption models, respectively. For Langmuir model, average variances between experimental and simulated concentrations of metal ions were in the range of 1.22-10.99 × 10(-3) and for the Freundlich model 0.12-3.98 × 10(-3), respectively. On the basis of previous facts, it is clear that developed integral bioprocess model with Freundlich model is more efficient in the prediction of concentration of metal ions in the HRTB. Furthermore, the results obtained also pointed out that the established model is at the same time accurate and robust and therefore it has great potential for use in the scale-up procedure.

  2. Coligand-directed synthesis of five Co(II)/Ni(II) coordination polymers with a neutral tetradentate ligand: syntheses, crystal structures, and properties.

    Science.gov (United States)

    Qin, Ling; Wang, Zhong-Jie; Wang, Ting; Zheng, He-Gen; Chen, Jin-Xi

    2014-09-07

    The solvothermal reactions of 1,1'-oxybis[3,5-di-4-pyridine]-benzene (L) and transition metal cations (Co and Ni) afford five novel coordination polymers in the presence of flexible bridging ligands (4,4'-H2nba = 4,4'-dicarboxydiphenylamine, H2cam = d-camphoric acid, 4,4'-H2sdb = 4,4'-sulfonyldibenzoic acid, H2chdc = 1,4-trans-cyclohexanedicarboxylic acid), namely {[Co2L2(OH)2(nba)]·2DMF}n (), {[CoL(cam)(H2O)]}n (), {[Co3(L)(4,4'-sdb)3(H2O)]·1.5CH3CN·4H2O}n (), {[Ni3(L)(4,4'-sdb)3(H2O)]·1.5CH3CN·4H2O}n (), and {[Ni2L2(chdc)2(H2O)2]·(H2O)3}n () (DMF = N,N-dimethylformamide). Their structures have been determined by single-crystal X-ray diffraction analyses and further characterized by elemental analyses, IR spectroscopy, and powder X-ray diffraction. Complex reveals a 2-fold interpenetrating three-dimensional (3D) framework with the Schläfli symbol {4·8·10(4)}{4·8·10} topology. Compound crystallizes in the achiral space group with the d-camphorate ligand racemized. Compounds and reveal similar structure with the {3·4(4)·6}{3(2)·4(8)·5(9)·6(9)} topology based on a linear trinuclear building block M3(OOCR)6 (M = Co(ii) or Ni(ii)). Compound is a wavy sheet, where both carboxylate and L ligands act as bidentate ligands. Moreover, UV-Visible absorption spectra of complexes , and the magnetic properties of have been investigated.

  3. Self-assembly, structures and properties of three new Ni (II ...

    Indian Academy of Sciences (India)

    Polymer 2 is a 1D wave-shaped chain derived from the 1D [Ni(L ¹)]n chain and monodentate coordinated 1,3,5-HBTC anions. Polymer 3 possesses an interesting 2D layer containing the trinuclear [Ni ₃ (1,3,5-BTC) ₂] substructural unit and 1D zigzag [Ni(L ²)]n chain, representing a 3,4-connected {6•8 ²} ₂{6 ² •8 ² • 10• 12} ...

  4. A Deep Narrowband Imaging Search for CIV and He II Emission from Ly$\\alpha$ Blobs

    OpenAIRE

    Battaia, Fabrizio Arrigoni; Yang, Yujin; Hennawi, Joseph F.; Prochaska, J. Xavier; Matsuda, Yuichi; Yamada, Toru; Hayashino, Tomoki

    2014-01-01

    We conduct a deep narrow-band imaging survey of 13 Ly$\\alpha$ blobs (LABs) located in the SSA22 proto-cluster at z~3.1 in the CIV and HeII emission lines in an effort to constrain the physical process powering the Ly$\\alpha$ emission in LABs. Our observations probe down to unprecedented surface brightness limits of 2.1 $-$ 3.4 $\\times$ 10$^{-18}$ erg s$^{-1}$ cm$^{-2}$ arcsec$^{-2}$ per 1 arcsec$^2$ aperture (5$\\sigma$) for the HeII$\\lambda$1640 and CIV$\\lambda$1549 lines, respectively. We do...

  5. Unusual Coexistence of Nickel(II) and Nickel(IV) in the Quadruple Perovskite Ba4Ni2Ir2O12 Containing Ir2NiO12 Mixed-Metal-Cation Trimers.

    Science.gov (United States)

    Ferreira, Timothy; Heald, Steve M; Smith, Mark D; Zur Loye, Hans-Conrad

    2018-03-19

    The crystal chemistry and magnetic properties of two hexagonal nickel(IV)-containing perovskites, Ba 4 Ni 1.94 Ir 2.06 O 12 and BaNiO 3 , are reported. The 12R perovskite, Ba 4 Ni 1.94 Ir 2.06 O 12 , possesses an unexpected coexistence of nickel(II) and nickel(IV). This quadruple perovskite structure contains Ir 2 NiO 12 mixed-metal-cation units in which direct metal-metal bonding between nickel(IV) and iridium(V) is inferred. X-ray absorption near-edge spectroscopy and X-ray photoelectron spectroscopy measurements were conducted to confirm the simultaneous presence of nickel(II) and nickel(IV).

  6. Preliminary screening of Ni(II metal tolerance and dye-decolorizing by Nocardiopsis sp. SD8

    Directory of Open Access Journals (Sweden)

    Ramasamy Thangaraj

    2016-04-01

    Full Text Available Objective: To reveal the screening of metal tolerance and dye-decolorizing of Nocardiopsis sp. Methods: NiSO4 and Congo red dye were used for evaluating the metal tolerance and dyedecolorizing of the randomly selected actinobacterial isolates. Results: Nocardiopsis sp. SD8 showed a better efficiency in Ni(II tolerance, though a longer lag phase was observed for this microorganism grown for 7 days in integrated mismatch negativity. Interestingly, we also found that Nocardiopsis sp. SD8 had dye-decolorizing, hemolytic, lipase and protease activity. Conclusions: The present results revealed the bioremediation of metal resistant and diverse properties of Nocardiopsis sp. SD8 and further investigations are needed to extract and identify the potent molecule.

  7. Development of Fast Response SME TiNi Foam Torque Tubes, Phase II

    Data.gov (United States)

    National Aeronautics and Space Administration — In Phase I, Shape Change Technologies had developed a process to manufacture net shape TiNi foam torque tubes that demonstrated the shape memory effect. The torque...

  8. Heavy Metals (Mg, Mn, Ni and Sn contamination in Soil Samples of Ahvaz II Industrial Estate of Iran in 2013

    Directory of Open Access Journals (Sweden)

    Soheil l Sobhanardakani

    2016-04-01

    Full Text Available Background & Aims of the Study: Due to the rapid industrial development in Khuzestan province of Iran during recent years, this study was performed to analyze the variation of metals concentrations (Mg, Mn, Ni, and Sn in soil samples of Ahvaz II Industrial estate during the spring season of 2013. Materials & Methods: In this experimental study, 27 topsoil samples were collected from nine stations. The intensity of the soil contamination was evaluated, using a contamination factor (Cf and geo-accumulation index (I-geo. Results:  The mean soil concentrations (in mg kg-1 (dry weight were in ranged within 870-1144 (Mg, 188-300 (Mn, 93-199 (Ni and 9-15 (Sn. The data indicated that the I-geo value for all metals falls in class ‘1’. Also the Cf value for Mg and Mn falls in class ‘0’, the Cf value for Sn falls in class ‘1’ and the Cf value for Ni falls in the classes of ‘1’ and ‘2’. The result of the Pearson correlation showed that there were significant positive associations between all metals. Conclusions: According to the results which were achieved by a cluster analysis, there were significant positive associations among all metals based on Pearson correlation coefficient, especially between Ni and Sn; also both of them with Mn. Because the Ni originates from oil sources it can be resulted that Mn and Sn originate from oil sources, too. Therefore, industrial activities and exploitation of oil reservoirs are the main cause of pollution in that area. Also, it can be concluded that, with increasing the distance from the source of pollution, the accumulation of contaminants in the soil samples decreased.

  9. Selective solid phase extraction of copper using a new Cu(II)-imprinted polymer and determination by inductively coupled plasma optical emission spectroscopy (ICP-OES).

    Science.gov (United States)

    Yilmaz, Vedat; Arslan, Zikri; Hazer, Orhan; Yilmaz, Hayriye

    2014-05-01

    This work reports the preparation of a novel Cu(II)-ion imprinted polymer using 2-thiozylmethacrylamide (TMA) for on-line preconcentration of Cu(II) prior to its determination by inductively coupled optical emission spectroscopy (ICP-OES). Cu(II)-TMA monomer (complex) was synthesized and copolymerized via bulk polymerization method in the presence of ethyleneglycoldimethacrylate cross-linker. The resulting polymer was washed with 5% (v/v) HNO 3 to remove Cu(II) ions and then with water until a neutral pH. The ion imprinted polymer was characterized by FT-IR and scanning electron microscopy. The experimental conditions were optimized for on-line preconcentration of Cu(II) using a minicolumn of ion imprinted polymer (IIP). Quantitative retention was achieved between pH 5.0 and 6.0, whereas the recoveries for the non-imprinted polymer (NIP) were about 61%. The IIP showed about 30 times higher selectivity to Cu(II) in comparison to NIP. The IIP also exhibited excellent selectivity for Cu(II) against the competing transition and heavy metal ions, including Cd, Co, Cr, Fe, Mn, Ni, Pb and Zn. Computational calculations revealed that the selectivity of IIP was mediated by the stability of Cu(II)-TMA complex which was far more stable than those of Co(II), Ni(II) and Zn(II) that have similar charge and ionic radii to Cu(II). A volume of 10 mL sample solution was loaded onto the column at 4.0 mL min -1 by using a sequential injection system (FIALab 3200) followed by elution with 1.0 mL of 2% (v/v) HNO 3 . The relative standard deviation (RSD) and limit of detection (LOD, 3s) of the method were 3.2% and 0.4 μg L -1 , respectively. The method was successfully applied to determination of Cu(II) in fish otoliths (CRM 22), bone ash (SRM 1400) and coastal seawater and estuarine water samples.

  10. Biosorption of Cd(II), Ni(II) and Pb(II) from aqueous solution by dried biomass of aspergillus niger: application of response surface methodology to the optimization of process parameters

    Energy Technology Data Exchange (ETDEWEB)

    Amini, Malihe; Younesi, Habibollah [Department of Environmental Science, Faculty of Natural Resources and Marine Sciences, Tarbiat Modares University, Noor (Iran)

    2009-10-15

    In this study, the biosorption of Cd(II), Ni(II) and Pb(II) on Aspergillus niger in a batch system was investigated, and optimal condition determined by means of central composite design (CCD) under response surface methodology (RSM). Biomass inactivated by heat and pretreated by alkali solution was used in the determination of optimal conditions. The effect of initial solution pH, biomass dose and initial ion concentration on the removal efficiency of metal ions by A. niger was optimized using a design of experiment (DOE) method. Experimental results indicated that the optimal conditions for biosorption were 5.22 g/L, 89.93 mg/L and 6.01 for biomass dose, initial ion concentration and solution pH, respectively. Enhancement of metal biosorption capacity of the dried biomass by pretreatment with sodium hydroxide was observed. Maximal removal efficiencies for Cd(II), Ni(III) and Pb(II) ions of 98, 80 and 99% were achieved, respectively. The biosorption capacity of A. niger biomass obtained for Cd(II), Ni(II) and Pb(II) ions was 2.2, 1.6 and 4.7 mg/g, respectively. According to these observations the fungal biomass of A. niger is a suitable biosorbent for the removal of heavy metals from aqueous solutions. Multiple response optimization was applied to the experimental data to discover the optimal conditions for a set of responses, simultaneously, by using a desirability function. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  11. Concentration of ions Co(II), Ni(II) at the Tokem-250 carboxylic cation exchange for catalysts development

    Science.gov (United States)

    Zharkova, Valentina; Bobkova, Ludmila; Brichkov, Anton; Kozik, Vladimir

    2017-11-01

    Sorption and catalytic properties of the cation exchanger are investigated. It was found that the Tokem-250 has a wide operating range of pH. The value of the effective ionization constant of the functional groups of the cation exchanger (pKa) is 6.59. The Tokem-250 cation exchanger exhibits selectivity to Ni2+ ions to Co2+ (D˜103). This is probably due to the stability of ion-exchange complexes detected by the method of diffuse reflectance electron spectroscopy (ESDD). According to these data, for Co2+ ions, in contrast to Ni2+, tetragonal distortion of octahedral coordination is characteristic, which has a positive effect on the stability of complexes with Co2+. To obtain spherical catalysts on the basis of Tokem-250, cobalt-containing samples of cation exchanger were used. The developed spherical materials have catalytic activity in the reactions of deep and partial oxidation of n-heptane.

  12. Emission-line diagnostics of nearby H II regions including interacting binary populations

    Science.gov (United States)

    Xiao, Lin; Stanway, Elizabeth R.; Eldridge, J. J.

    2018-03-01

    We present numerical models of the nebular emission from H II regions around young stellar populations over a range of compositions and ages. The synthetic stellar populations include both single stars and interacting binary stars. We compare these models to the observed emission lines of 254 H II regions of 13 nearby spiral galaxies and 21 dwarf galaxies drawn from archival data. The models are created using the combination of the Binary Population and Spectral Synthesis (BPASS) code with the photoionization code CLOUDY to study the differences caused by the inclusion of interacting binary stars in the stellar population. We obtain agreement with the observed emission line ratios from the nearby star-forming regions and discuss the effect of binary star evolution pathways on the nebular ionization of H II regions. We find that at population ages above 10 Myr, single-star models rapidly decrease in flux and ionization strength, while binary-star models still produce strong flux and high [O III]/Hβ ratios. Our models can reproduce the metallicity of H II regions from spiral galaxies but we find higher metallicities than previously estimated for the H II regions from dwarf galaxies. Comparing the equivalent width of Hβ emission between models and observations, we find that accounting for ionizing photon leakage can affect age estimates for H II regions. When it is included, the typical age derived for H II regions is 5 Myr from single-star models, and up to 10 Myr with binary-star models. This is due to the existence of binary-star evolution pathways which produce more hot WR and helium stars at older ages. For future reference, we calculate new BPASS binary maximal starburst lines as a function of metallicity, and for the total model population, and present these in Appendix A.

  13. Enhanced methane emissions from tropical wetlands during the 2011 la Niña

    NARCIS (Netherlands)

    Pandey, Sudhanshu; Houweling, Sander; Krol, Maarten C.; Aben, Ilse; Monteil, Guillaume; Nechita-Banda, Narcisa; Dlugokencky, Edward J.; Detmers, Rob; Hasekamp, Otto; Xu, Xiyan; Riley, William J.; Poulter, Benjamin; Zhang, Zhen; McDonald, Kyle C.; White, James W.C.; Bousquet, Philippe; Röckmann, Thomas

    2017-01-01

    Year-to-year variations in the atmospheric methane (CH4) growth rate show significant correlation with climatic drivers. The second half of 2010 and the first half of 2011 experienced the strongest La Niña since the early 1980s, when global surface networks started monitoring atmospheric CH4 mole

  14. Axially chiral Ni(II) complexes of α-amino acids: Separation of enantiomers and kinetics of racemization.

    Science.gov (United States)

    Zhang, Wenzhong; Ekomo, Romuald Eto; Roussel, Christian; Moriwaki, Hiroki; Abe, Hidenori; Han, Jianlin; Soloshonok, Vadim A

    2018-04-01

    Herein we present design, synthesis, chiral HPLC resolution, and kinetics of racemization of axially chiral Ni(II) complexes of glycine and di-(benzyl)glycine Schiff bases. We found that while the ortho-fluoro derivatives are configurationally unstable, the pure enantiomers of corresponding axially chiral ortho-chloro-containing complexes can be isolated by preparative HPLC and show exceptional configurational stability (t 1/2 from 4 to 216 centuries) at ambient conditions. Synthetic implications of this discovery for the development of new generation of axially chiral auxiliaries, useful for general asymmetric synthesis of α-amino acids, are discussed. © 2018 Wiley Periodicals, Inc.

  15. Early positron emission tomography response-adapted treatment in stage I and II hodgkin lymphoma

    DEFF Research Database (Denmark)

    André, Marc P.E.; Girinsky, Théodore; Federico, Massimo

    2017-01-01

    Purpose Patients who receive combined modality treatment for stage I and II Hodgkin lymphoma (HL) have an excellent outcome. Early response evaluation with positron emission tomography (PET) scan may improve selection of patients who need reduced or more intensive treatments. Methods We performed...

  16. Interactions among energy consumption, economic development and greenhouse gas emissions in Japan after World War II

    Science.gov (United States)

    The long-term dynamic changes in the triad, energy consumption, economic development, and Greenhouse gas (GHG) emissions, in Japan after World War II were quantified, and the interactions among them were analyzed based on an integrated suite of energy, emergy and economic indices...

  17. Study of the emission oxidative reactions of ruthenium (II) complex by cationic compounds in anionic micelles

    International Nuclear Information System (INIS)

    Bonilha, J.B.S.

    1985-01-01

    The oxidative quenching of the emission of the tetraanionic complex tris (4,4' dicarboxylate - 2,2' - bipyridine ruthenium (II) in aqueous solution, by both organic and inorganic compounds in presence of anionic detergents, above and below the critical micelle concentration is studied. The organic cations, the inorganic ion and detergents used are shown. (M.J.C.) [pt

  18. Template-Mediated Ni(II) Dispersion in Mesoporous SiO2for Preparation of Highly Dispersed Ni Catalysts: Influence of Template Type.

    Science.gov (United States)

    Ning, Xin; Lu, Yiyuan; Fu, Heyun; Wan, Haiqin; Xu, Zhaoyi; Zheng, Shourong

    2017-06-07

    Supported Ni catalysts on three mesoporous SiO 2 supports (i.e., SBA-15, MCM-41, and HMS) were prepared using a solid-state reaction between Ni(NO 3 ) 2 and organic template-occluded mesoporous SiO 2 . For comparison, supported Ni catalysts on mesoporous SiO 2 synthesized by the conventional impregnation method were also included. The catalysts were characterized by scanning electron microscopy, X-ray diffraction, UV-vis diffuse reflectance spectroscopy, N 2 adsorption, X-ray photoelectron spectroscopy, H 2 temperature-programmed reduction, transmission electron microscopy, and transmission electron microscopy-energy-dispersive X-ray. The catalytic properties of the catalysts were evaluated using gas-phase catalytic hydrodechlorination of 1,2-dichloroethane. The results showed that upon grinding Ni(NO 3 ) 2 with template-occluded mesoporous SiO 2 , strong coordination between Ni 2+ and dodecylamine was identified in the Ni(NO 3 ) 2 -HMS system. Additionally, the results of H 2 temperature-programmed reduction revealed that NiO in calcined NiO/HMS was reduced at higher temperature than those in calcined NiO/SBA-15 and NiO/MCM-41, reflecting the presence of a strong interaction between NiO and mesoporous SiO 2 in NiO/HMS. Consistently, the average particle sizes of metallic Ni were found to be 2.7, 3.4, and 9.6 nm in H 2 -reduced Ni/HMS, Ni/SBA-15, and Ni/MCM-41, respectively, indicative of a much higher Ni dispersion in Ni/HMS. For the catalytic hydrodechlorination of 1,2-dichloroethane, Ni/MCM-41 synthesized by the solid-state reaction method exhibited a catalytic activity similar to that prepared by the impregnation method, while higher catalytic activities were observed on Ni/HMS and Ni/SBA-15 than on their counterparts prepared by the impregnation method. Furthermore, a higher conversion was identified on Ni/HMS than on Ni/SBA-15 and Ni/MCM-41, highlighting the importance of template type for the preparation of highly dispersed metal catalysts on mesoporous Si

  19. Cu(II) and Ni(II) 4-cyanobenzoate complexes with nicotinamide: Synthesis, spectral, structural and optical characterization and thermal behavior

    Science.gov (United States)

    Özbek, Füreya Elif; Sertçelik, Mustafa; Yüksek, Mustafa; Necefoğlu, Hacali; Çelik, Raziye Çatak; Nayir, Gamze Yılmaz; Hökelek, Tuncer

    2017-12-01

    Two new copper(II) and nickel(II) complexes [M(NCsbnd C6H4COO)2(C6H6N2O)2(H2O)2] (where M:Cu and Ni) have been synthesized and characterized by elemental analysis, FT-IR and UV-Vis spectroscopy, spectroscopic ellipsometer (SE), X-ray crystallography, thermal analysis and molar conductivity. X-ray measurements showed that both of the complexes crystallized in triclinic system with the space group P-1. The isostructure complexes have distorted octahedral geometry around the metal atom center. In both of the crystal structures, the metal atoms are coordinated by two nitrogen atoms from two different nicotinamide ligands, two carboxyl oxygen atoms from two different 4-cyanobenzoate anions and two oxygen atoms from two different water molecules. From the linear absorption spectra and spectroscopic ellipsometer measurements, it was observed that these complexes showed different optical behaviors.

  20. Synthesis of Ni(II) and Cu(II) complexes with N-(benzylcarbamothioyl) benzamide as corrosion inhibitors for mild steel in 1M HCl

    Science.gov (United States)

    Kassim, Karimah; Nordin, Nurul Atikah; Zulkifli, Norsakina Zurina; Hashim, Nor Zakiah Nor

    2017-11-01

    In this study, N-(benzylcarbamothioyl) benzamide(A1) with its Cu(II) and Ni(II) complexes were successfully synthesized using condensation method. The synthesized compounds were characterized by elemental analysis (CHNS), IR spectroscopy, NMR (1H) spectroscopy and melting point analysis. The synthesized compounds have been evaluated as new inhibitors for the corrosion of mild steel in 1M HCl solution using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) techniques. Polarization measurements showed that these derivatives are anodic-type inhibitors. The inhibition efficiency of inhibitors increased with an increase the concentration of inhibitors. Nyquist plots showed depressed semicircles with their centre below real axis. From the results, it showed the inhibition efficiency of thiourea complexes were higher than the ligands due its larger size.

  1. Emissions from residential combustion considering end-uses and spatial constraints: Part II, emission reduction scenarios

    Science.gov (United States)

    Winijkul, Ekbordin; Bond, Tami C.

    2016-01-01

    Cooking, heating, and other activities in the residential sector are major sources of indoor and outdoor air pollution, especially when solid fuels are used to provide energy. Because of their deleterious effects on the atmosphere and human health, multinational strategies to reduce emissions have been proposed. This study examines the effects of some possible policies, considering realistic factors that constrain mitigation: end-uses, spatial constraints involving proximity to forest or electricity, existing technology, and assumptions about user behavior. Reduction scenarios are applied to a year-2010, spatially distributed baseline of emissions of particulate matter, black carbon, organic carbon, nitrogen oxides, methane, non-methane hydrocarbons, carbon monoxide, and carbon dioxide. Scenarios explored are: (1) cleanest current stove, where we assume that existing technology in each land type is applied to burn existing fuels; (2) stove standards, where we assume that stoves are designed to meet performance standards; and (3) clean fuels, where users adopt the cleanest fuels plausible in each land type. We assume that people living in forest access areas continue to use wood regardless of available fuels, so the clean-fuels scenario leads to a reduction in emissions of 18-25%, depending on the pollutant, across the study region. Cleaner stoves preferentially affect land types with forest access, where about half of the fuel is used; emission reductions range from 25 to 82%, depending on the pollutant. If stove performance standards can be met, particulate matter emissions are reduced by 62% for the loosest standards and 95% for the tightest standards, and carbon monoxide is reduced by 40% and 62% for the loosest and tightest standards. Reductions in specific regions and countries depend on the existing fuel mixture and the population division among land types, and are explored for Latin America, Africa, East Asia, South Asia, and Southeast Asia.

  2. Scanning tunneling microscopy investigation of nano-structured α-K5PW11(M x OH2)O39(M = Mn(II), Co(II), Ni(II), and Zn(II)) Keggin heteropolyacid catalyst monolayers.

    Science.gov (United States)

    Choi, Jung Ho; Kang, Tae Hun; Bang, Yongju; Yoo, Jaekyeong; Jun, Jin Oh; Song, In Kyu

    2014-11-01

    Nano-structured α-K5PW11(M x OH2)O39 (M = Mn(II), Co(II), Ni(II), and Zn(II)) Keggin heteropolyacids (HPAs) were investigated by scanning tunneling microscopy (STM) and tunneling spectroscopy (TS) measurements in order to elucidate their redox property and oxidation catalysis. HPA molecules formed two-dimensional self-assembled monolayer arrays on highly oriented pyrolytic graphite (HOPG) surface. Furthermore, HPAs exhibited a distinctive current-voltage behavior referred to as negative differential resistance (NDR) phenomenon. The measured NDR peak voltage of HPAs was correlated with the reduction potential and the absorption edge energy determined by electrochemical method and UV-visible spectroscopy, respectively. NDR peak voltage of HPAs appeared at less negative voltage with increasing reduction potential and with decreasing UV-visible absorption edge energy. The correlations strongly suggested that NDR phenomenon was closely related to the redox property of HPAs. Vapor-phase oxidation of benzyl alcohol to benzaldehyde was carried out as a model reaction to track the oxidation catalysis of HPAs. NDR peak voltage appeared at less negative voltage with increasing yield for benzaldehyde.

  3. Transition probabilities for lines of Cr II, Na II and Sb I by laser produced plasma atomic emission spectroscopy

    International Nuclear Information System (INIS)

    Gonzalez, A. M.; Ortiz, M.; Campos, J.

    1995-01-01

    Absolute transition probabilities for lines of CR II, Na II and Sb I were determined by emission spectroscopy of laser induced plasmas. the plasma was produced focusing the emission of a pulsed Nd-Yag laser on solid samples containing the atom in study. the light arising from the plasma region was collected by and spectrometer. the detector used was a time-resolved optical multichannel analyzer (OMA III EG and G). The wavelengths of the measured transitions range from 2000 sto 4100 A. The spectral resolution of the system was 0. 2 A. The method can be used in insulators materials as Cl Na crystals and in metallic samples as Al-Cr and Sn-Sn alloys. to avoid self-absorption effects the alloys were made with low Sb or Cr content. Relative transition probabilities have been determined from measurements of emission-line intensities and were placed on an absolute scale by using, where possible, accurate experimental lifetime values form the literature or theoretical data. From these measurements, values for plasma temperature (8000-24000 K), electron densities (∼∼ 10''16 cm ''-3) and self-absorption coefficients have been obtained. (Author) 56 refs

  4. Transition probabilities for lines of Cr II, Na II and Sb I by laser produced plasma atomic emission spectroscopy

    International Nuclear Information System (INIS)

    Gonzalez, A.M.; Ortiz, M.; Campos, J.

    1995-09-01

    Absolute transition probabilities for lines of Cr II, Na II and Sb I were determined by emission spectroscopy of laser induced plasmas. The plasma was produced focusing the emission of a pulsed Nd-Yag laser on solid samples containing the atom in study. The light arising from the plasma region was collected by and spectrometer. the detector used was a time-resolved optical multichannel analyzer (OMA III EG and G). The wavelengths of the measured transitions range from 2000 to 4100 A. The spectral resolution of the system was 0.2 A. The method can be used in insulators materials as Cl Na crystals and in metallic samples as Al-Cr and Sn-Sb alloys. To avoid self-absorption effects the alloys were made with low Sb or Cr content. Relative transition probabilities have been determined from measurements of emission-line intensities and were placed on an absolute scale by using, where possible, accurate experimental lifetime values form the literature or theoretical data. From these measurements, values for plasma temperature (8000-24000K), electron densities (approx 10 ''16 cm''-3) and self-absorption coefficients have been obtained

  5. Structural, thermal, biological and semiconducting properties of Mn(II), Fe(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and VO(IV) complexes of Schiff base derived from resdiacetophenone and S-benzyldithiocarbazate

    International Nuclear Information System (INIS)

    Makode, J.T.; Bhadange, S.G.; Aswar, A.S.

    2003-01-01

    A series of Mn(II), Fe(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and VO(IV) complexes with Schiff base derived from resdiacetophenone and S-benzyldithiocarbazate have been synthesized and characterized by elemental analysis, magnetic moment, IR and electronic spectral studies and thermal analysis. The Schiff base functions as a binucleating tridentate chelating agent and coordinates via the deprotonated phenolic oxygen, azomethine nitrogen and thioenolate sulphur atoms to the metal ion favouring the formation of bimetallic complexes. From dynamic TG data, activation energy and other kinetic parameters have been computed using Freeman-Carroll-Wentworth and Coats-Redfern methods. Electrical conductivity of the complexes have also been studied between 313-473 in pellet forms and the complexes are found to exhibit semiconducting behaviour. The antimicrobial activity of the ligand and its complexes have been screened against various microorganisms and all of them found to be moderately active against the organisms. (author)

  6. A metal-organic framework nanocomposite made from functionalized magnetite nanoparticles and HKUST-1 (MOF-199) for preconcentration of Cd(II), Pb(II), and Ni(II)

    International Nuclear Information System (INIS)

    Ghorbani-Kalhor, Ebrahim

    2016-01-01

    The author describes the preparation of a magnetic metal organic framework of type MOF-199 containing magnetite (Fe 3 O 4 ) nanoparticles carrying covalently immobilized 4-(thiazolylazo) resorcinol (Fe 3 O 4 -TAR). This material is shown to represent a viable sorbent for separation and preconcentration of Cd(II), Pb(II), and Ni(II) ions. Box-Behnken design was applied to optimize the parameters affecting preconcentration. Following elution with 0.6 mol L −1 EDTA, the ions were quantified by FAAS. The capacity of the sorbent ranged between 185 and 210 mg g −1 . The limits of detection are 0.15, 0.40, and 0.8 ng mL −1 for Cd(II), Ni(II), and Pb(II) ions, respectively. The relative standard deviations are <8.5 %. The method was successfully applied to the rapid extraction of trace amounts of these ions from sea food and agri food. (author)

  7. Studies of Olefin Dimerization, Oligomerization, and Polymerization Catalyzed by Cationic (alpha-Diimine)Ni(II) Complexes

    National Research Council Canada - National Science Library

    Svejda, Steven

    1999-01-01

    .... The development of cationic (alpha-diimine)nickel(II) and palladium(II) complexes which catalyze the polymerization of both ethylene and alpha-olefins to high polymers represents a major advance in the field of olefin polymerization catalysis...

  8. Ternary complexes metal [Co(II), Ni(II), Cu(II) and Zn(II)]--ortho-iodohippurate (I-hip)--acyclovir. X-ray characterization of isostructural [(Co, Ni or Zn)(I-hip)(2)(ACV)(H(2)O)(3)] with stacking as a recognition factor.

    Science.gov (United States)

    Barceló-Oliver, M; Terrón, A; García-Raso, A; Fiol, J J; Molins, E; Miravitlles, C

    2004-11-01

    Four ternary metal--ortho-iodohippurate (I-hip)--acyclovir (ACV) complexes, [M(I-hip)(2)(ACV)(H(2)O)(3)] where M is Co(II) (1), Ni(II) (2), Cu (3) and Zn(II) have been obtained by reaction between the corresponding binary complexes M(II)(I-hip)(2)xnH(2)O and ACV. Three ternary complexes (M=Co, Ni and Zn) and the corresponding Zn(II)--ortho-iodohippurate binary derivative have been structurally characterized by X-ray diffraction: The studies show these three ternary complexes are isostructural and present, in solid state, an interesting stacking between the nucleobase and the aryl ring of the hippurate moiety, which probably promotes the formation of ternary complexes. Moreover, the two different ligands interact between them by means of ancillary hydrogen bonds with water molecules coordinated to the metal ion. It must be mentioned that these two recognition factors, hydrogen bonds plus stacking, could explain the reason for the isostructurality of these ternary derivatives with so different three metal ions, with diverses trends in coordination numbers and geometries. In solid state, there are two enantiomeric molecules that are related by an inversion center as the crystal-building unit (as a translational motif) for the ternary complexes.

  9. An experimental and theoretical magneto-structural study of polynuclear Ni(II) complexes assembled from a versatile bis(salicylaldehyde)diamine polytopic ligand.

    Science.gov (United States)

    Oyarzabal, Itziar; Ruiz, José; Mota, Antonio J; Rodríguez-Diéguez, Antonio; Seco, José M; Colacio, Enrique

    2015-04-21

    Six novel Ni(II) complexes, ranging from mononuclear to tetranuclear, have been prepared from the polytopic symmetrical Mannich base ligand N,N'-dimethyl-N,N'-bis(2-hidroxy-3-formyl-5-bromo-benzyl)ethylenediamine (H2L) and different anionic coligands: [Ni(H2L)(NO3)(H2O)]NO3·H2O (), [Ni2(μ-L)(acac)2(H2O)]·CH3CN (), [Ni2(μ-L)(μ-OAc)(NCS)] (), [Ni3(μ-L)2(μ-OH2)2(H2O)(CH3CN)](NO3)2·4CH3CN (), [Ni4(μ-L)2(μ-OAc)2(μ-OCH3)2]·6H2O·2CH3OH () and [Ni4(μ-L)2(μ-OAc)2(μ-N3)2]·2H2O·CH3OH (). These complexes have been characterized by single crystal X-ray diffraction, magnetic measurements and DFT theoretical calculations. The structural analysis of these complexes reveals that the anionic coligand and reaction conditions play a fundamental role in determining their final structures and magnetic properties. Compound contains a monomeric cationic unit with the nickel ion coordinated in the external O4 site of the compartmental ligand H2L, which acts in a neutral zwitterionic form. Complexes and are dinuclear Ni2 neutral entities, in which the Ni(II) ions are connected through two μ-phenoxido bridging groups. The Ni(O)2Ni bridging fragment in is almost planar, whereas in is bent due to the additional presence of a syn-syn acetate bridge connecting the Ni(II) atoms. Complex has a bent trinuclear structure with double μ-phenoxido/μ-water bridges between the central and terminal nickel atoms. Complexes and are Ni4 complexes with defective dicubane structures, in which triple μ-phenoxido/μ1,1,1-X/syn-syn acetate and double μ-phenoxido/μ1,1,1-X mixed bridges connect central and terminal Ni(II) atoms, whereas double μ1,1,1-X bridging ligands link the central Ni(II) ions (X = methoxido and azido groups for and , respectively). Magnetic susceptibility measurements reveal that complex shows a moderate antiferromagnetic interaction between the Ni(II) ions through the double di-μ-phenoxido bridge, leading to a S = 0 ground state. Compared to , complex shows a much

  10. Sorption of Cu(II, Zn(II and Ni(II from aqueous solution using activated carbon prepared from olive stone waste

    Directory of Open Access Journals (Sweden)

    Gehan Sharaf

    2015-10-01

    Full Text Available The performance of olive stone activated carbon (OSAC for sorption of Cu2+, Zn2+ and Ni2+ ions was investigated via batch technique. OSAC materials were prepared under different physially activation conditions. Olive stone waste was physically activated with N2 gas and steam gas at 900oC at 3.5h hold time (OSAC-3 was choice as the best one for Cu2+, Zn2+ and Ni2+ removal. Characterization for OSAC-3 were performed under BET-surface area, SEM, density and FTIR-spectrum. Optimum adsorption conditions were specified as a function of agitation time, initial metal concentration, pH and temperature. Kinetic results were found to be fast and described well by the pseudo-second order model. The adsorption capacities are 25.38mg/g (Cu2+, 16.95mg/g (Zn2+ and 14.65mg/g (Ni2+ which followed the sequence Cu2+ > Zn2+ > Ni2+. Spontaneous adsorption for all the studied cations, endothermic nature for both Zn2+ and Ni2+ ions and exothermic nature for Cu2+ ions were obtained. The results showed that OSAC-3 is a good economical material for Cu2+, Zn2+ and Ni2+ remediation from weakly acidic contaminated effluents.

  11. THE LOCAL [C ii] 158 μ m EMISSION LINE LUMINOSITY FUNCTION

    Energy Technology Data Exchange (ETDEWEB)

    Hemmati, Shoubaneh; Yan, Lin; Capak, Peter; Faisst, Andreas; Masters, Daniel [Infrared Processing and Analysis Center, Department of Astronomy, California Institute of Technology, 1200 E. California Blvd., Pasadena CA 91125 (United States); Diaz-Santos, Tanio [Nucleo de Astronomia de la Facultad de Ingenieria, Universidad Diego Portales, Av. Ejercito Libertador 441, Santiago (Chile); Armus, Lee, E-mail: shemmati@ipac.caltech.edu [Spitzer Science Center, Department of Astronomy, California Institute of Technology, 1200 E. California Blvd., Pasadena, CA 91125 (United States)

    2017-01-01

    We present, for the first time, the local [C ii] 158 μ m emission line luminosity function measured using a sample of more than 500 galaxies from the Revised Bright Galaxy Sample. [C ii] luminosities are measured from the Herschel PACS observations of the Luminous Infrared Galaxies (LIRGs) in the Great Observatories All-sky LIRG Survey and estimated for the rest of the sample based on the far-infrared (far-IR) luminosity and color. The sample covers 91.3% of the sky and is complete at S{sub 60μm} > 5.24 Jy. We calculate the completeness as a function of [C ii] line luminosity and distance, based on the far-IR color and flux densities. The [C ii] luminosity function is constrained in the range ∼10{sup 7–9} L{sub ⊙} from both the 1/ V{sub max} and a maximum likelihood methods. The shape of our derived [C ii] emission line luminosity function agrees well with the IR luminosity function. For the CO(1-0) and [C ii] luminosity functions to agree, we propose a varying ratio of [C ii]/CO(1-0) as a function of CO luminosity, with larger ratios for fainter CO luminosities. Limited [C ii] high-redshift observations as well as estimates based on the IR and UV luminosity functions are suggestive of an evolution in the [C ii] luminosity function similar to the evolution trend of the cosmic star formation rate density. Deep surveys using the Atacama Large Millimeter Array with full capability will be able to confirm this prediction.

  12. Synergistic effect of graphene nanosheets and zinc oxide nanoparticles for effective adsorption of Ni (II) ions from aqueous solutions

    Science.gov (United States)

    Hadadian, Mahboubeh; Goharshadi, Elaheh K.; Fard, Mina Matin; Ahmadzadeh, Hossein

    2018-03-01

    The threat of toxic substances such as heavy metals to public health and wildlife has led to an increasing public awareness. Different techniques for neutralizing the toxic effects of heavy metals in wastewater have been used. Here, we prepared a new and efficient type of adsorbent, zinc oxide-graphene nanocomposite (ZnO-Gr), via a green method to remove Ni (II) ions from aqueous solutions. A facile microwave-assisted hydrothermal technique in the presence of an ionic liquid, 1-hexyl-3-methylimidazolium bis (trifluoromethylsulfonyl) imide [C6mim] [NTf2], was used to prepare ZnO-Gr. The synergistic effect between graphene nanosheets and ZnO nanoparticles in this new adsorbent for Ni (II) ions caused a maximum adsorption capacity of 66.7 mg g-1 at room temperature which is much higher than that of graphene nanosheets (3.8 mg g-1) and other carbonaceous nanomaterials used as an adsorbent in the literature. The maximum desorption percentage (90.32%) was achieved at pH 3.6. By thermodynamic study, we found that the adsorption of this heavy metal ion on ZnO-Gr was spontaneous (Δ G° = -6.14 kJ mol-1) and endothermic (Δ H° = 53.31 kJ mol-1) with entropy change of Δ S° = 199.45 J K-1 mol- 1.

  13. ENANTIOSELECTIVE CONJUGATE ADDITION OF DIETHYLZINC TO CHALCONES CATALYZED BY CHIRAL NI(II) AMINOALCOHOL COMPLEXES

    NARCIS (Netherlands)

    DEVRIES, AHM; JANSEN, JFGA; FERINGA, BL

    1994-01-01

    Conjugate addition of diethylzinc to chalcones is catalysed by complexes prepared in situ from Ni(acac)(2) and cis-exo-N,N-dialkyl-3-aminoisoborneols or (+)-cis-endo-N,N-dimethyl-3-aminoborneol ((+)- DAB) (13b). The products are obtained with enantioselectivities up to 84 %. When scalemic

  14. Enantioselective Conjugate Addition of Diethylzinc to Chalcones Catalysed by Chiral Ni(II) Aminoalcohol Complexes

    NARCIS (Netherlands)

    Vries, André H.M. de; Jansen, Johan F.G.A.; Feringa, Bernard

    1994-01-01

    Conjugate addition of diethylzinc to chalcones is catalysed by complexes prepared in situ from Ni(acac)2 and cis-exo-N,N-dialkyl-3-aminoisoborneols or (+)-cis-endo-N,N-dimethyl-3-aminoborneol ((+)-DAB) (13b). The products are obtained with enantioselectivities up to 84 %. When scalemic

  15. Investigation on the Synergistic Complexation of Ni(II with 1,10-Phenanthroline and Dithizone at Hexane-Water Interface Using Centrifugal Liquid Membrane-Spectrophotometry

    Directory of Open Access Journals (Sweden)

    Yoki Yulizar

    2012-12-01

    Full Text Available Complex formation of Ni(II and 1,10-phenanthroline (C12H8N2/Phen with the addition of dithizone (C13H12N4S/HDz at the hexane-water interface has been studied by direct measurement spectrophotometry using the centrifugal liquid membrane (CLM method. Ni(II ion with Phen formed a cationic complex of Ni(C12H8N222+ or NiPhen22+. That complex dissolved in the aqueous phase and had two UV absorption spectrum maxima wavelengths, max 270 and 292 nm. Observation of complex formation was performed variations of pH and ligand concentration. The pH caused protonation that affected the amount of the formed complex. With the variations of ligand concentrations, the greater was the concentration of ligands the greater was the formed complex. Based on the Batch method, the HDz ligand addition into the NiPhen22+ cationic complex produced ion association complex of Ni(C13H11N4S2(C12H8N2 or NiDz2Phen at max 403 nm, and is extracted in the organic phase. Measurement results using CLM method showed that NiDz2Phen complex was formed at hexane-water interface with max 523 nm. Comparison of Phen with HDz ligand concentrations affected the initial formation rate of NiDz2Phen complex. The greater concentration of Phen ligand increased the initial rate of formation for synergistic complex. The obtained data using CLM method indicated that the synergistic complex formation rate constant of NiDz2Phen at the interface, k was 0.30 s-1.

  16. Effects of gasoline property on exhaust emission; Gasoline sosei ga haishutsu gas ni oyobosu eikyo

    Energy Technology Data Exchange (ETDEWEB)

    Kameoka, A.; Tsuruga, F.; Hosoi, K. [Japan Automobile Research Institute Inc., Tsukuba (Japan)

    1998-10-15

    In order to clarify the impact factors of gasoline property on emission gas, continuous measurement and behavior analysis of emission gas were carried out during running of vehicles. Two passenger vehicles of 2L (A) and 2.5L (B) in total displacement, catalyst aged for hours equivalent to 10,000km running and dummy catalyst with no catalytic effects were used for the experiment. A learning control system was also adopted only for the vehicle A. In 11 mode running, CO, THC and NOx emissions increased with aromatic content in gasoline in No.1 trip. In 10/15 mode running, although CO and THC emissions increased with aromatic content in gasoline, the amount of NOx emission was dependent on the kind of vehicles. On the vehicle B with no learning control system, it was probably derived from the fact that an air excess rate increases with an increase in fuel mass by supplying high-density high-aromatic gasoline. CO, THC and NOx increased with sulfur content in gasoline. In particular, the sulfur content had a large effect on NOx emission. 2 refs., 13 figs., 2 tabs.

  17. Importance of reduced sulfur for the equilibrium chemistry and kinetics of Fe(II), Co(II) and Ni(II) supplemented to semi-continuous stirred tank biogas reactors fed with stillage.

    Science.gov (United States)

    Shakeri Yekta, Sepehr; Lindmark, Amanda; Skyllberg, Ulf; Danielsson, Asa; Svensson, Bo H

    2014-03-30

    The objective of the present study was to assess major chemical reactions and chemical forms contributing to solubility and speciation of Fe(II), Co(II), and Ni(II) during anaerobic digestion of sulfur (S)-rich stillage in semi-continuous stirred tank biogas reactors (SCSTR). These metals are essential supplements for efficient and stable performance of stillage-fed SCSTR. In particular, the influence of reduced inorganic and organic S species on kinetics and thermodynamics of the metals and their partitioning between aqueous and solid phases were investigated. Solid phase S speciation was determined by use of S K-edge X-ray absorption near-edge spectroscopy. Results demonstrated that the solubility and speciation of supplemented Fe were controlled by precipitation of FeS(s) and formation of the aqueous complexes of Fe-sulfide and Fe-thiol. The relatively high solubility of Co (∼ 20% of total Co content) was attributed to the formation of compounds other than Co-sulfide and Co-thiol, presumably of microbial origin. Nickel had lower solubility than Co and its speciation was regulated by interactions with FeS(s) (e.g. co-precipitation, adsorption, and ion substitution) in addition to precipitation/dissolution of discrete NiS(s) phase and formation of aqueous Ni-sulfide complexes. Copyright © 2014 Elsevier B.V. All rights reserved.

  18. Search for proton emission in {sup 54}Ni and multi-nucleon transfer reactions in the actinide region

    Energy Technology Data Exchange (ETDEWEB)

    Geibel, Kerstin

    2012-06-15

    The first part of the thesis presents the investigation of fusion-evaporation reactions in order to verify one-proton emission from the isomeric 10{sup +} state in the proton rich nucleus {sup 54}Ni. Between the years 2006 and 2009 a series of experimental studies were performed at the Tandem accelerator in the Institut fuer Kernphysik (IKP), University of Cologne. These experiments used fusion-evaporation reactions to populate {sup 54}Ni via the two-neutron-evaporation channel of the compound nucleus {sup 56}Ni. The cross section for the population of the ground state of {sup 54}Ni was predicted to be in orders of microbarn. This required special care with respect to the sensitivity of the experimental setup, which consisted of a double-sided silicon-strip detector (DSSSD), a neutron-detector array and HPGe detectors. In two experiments the excitation functions of the reactions ({sup 32}S+{sup 24}Mg) and ({sup 28}Si+{sup 28}Si) were determined to find the optimal experimental conditions for the population of {sup 54}Ni. A final experiment employed a {sup 28}Si beam at an energy of 70 MeV, impinging on a {sup 28}Si target. With a complex analysis it is possible to obtain a background-free energy spectrum of the DSSSD. An upper cross section limit for the population of the 10{sup +} state in {sup 54}Ni is established at σ({sup 54}Ni(10{sup +})) ≤ (13.9 ± 7.8) nbarn. In the second part of the thesis the population of actinide nuclei by multi-nucleon transfer reactions is investigated. Two experiments, performed in 2007 and 2008 at the CLARA-PRISMA setup at the Laboratori Nazionali di Legnaro, are analyzed with respect to the target-like reaction products. In both experiments {sup 238}U was used as target. A {sup 70}Zn beam with 460 MeV and a {sup 136}Xe beam with 926 MeV, respectively, impinged on the target, inducing transfer reactions. Kinematic correlations between the reaction partners are used to obtain information on the unobserved target-like reaction

  19. Effect of Molecular Guest Binding on the d-d Transitions of Ni2+of CPO-27-Ni: A Combined UV-Vis, Resonant-Valence-to-Core X-ray Emission Spectroscopy, and Theoretical Study.

    Science.gov (United States)

    Gallo, Erik; Gorelov, Evgeny; Guda, Alexander A; Bugaev, Aram L; Bonino, Francesca; Borfecchia, Elisa; Ricchiardi, Gabriele; Gianolio, Diego; Chavan, Sachin; Lamberti, Carlo

    2017-12-04

    We used Ni K-edge resonant-valence-to-core X-ray emission spectroscopy (RVtC-XES, also referred to as direct RIXS), an element-selective bulk-sensitive synchrotron-based technique, to investigate the electronic structure of the CPO-27-Ni metal-organic framework (MOF) upon molecular adsorption of significant molecular probes: H 2 O, CO, H 2 S, and NO. We compare RVtC-XES with UV-vis spectroscopy, and we show that the element selectivity of RVtC-XES is of strategic significance to observe the full set of d-d excitations in Ni 2+ , which are partially overshadowed by the low-energy π-π* transitions of the Ni ligands in standard diffuse-reflectance UV-vis experiments. Our combined RVtC-XES/UV-vis approach provides access to the whole set of d-d excitations, allowing us a complete discussion of the changes undergone by the electronic configuration of the Ni 2+ sites hosted within the MOF upon molecular adsorption. The experimental data have been interpreted by multiplet ligand-field theory calculations based on Wannier orbitals. This study represents a step further in understanding the ability of the CPO-27-Ni MOFs in molecular sorption and separation applications.

  20. Fluorescence-detected X-ray magnetic circular dichroism of well-defined Mn(II) and Ni(II) doped in MgO crystals: credential evaluation for measurements on biological samples.

    Science.gov (United States)

    Wang, Hongxin; Bryant, Craig; LeGros, M; Wang, Xin; Cramer, S P

    2012-10-18

    L(2,3)-edge X-ray magnetic circular dichroism (XMCD) spectra have been measured for the well-defined dilute Ni(II) and Mn(II) ions doped into a MgO crystal, with sub-Kelvin dilution refrigerator cooling and 2 T magnetic field magnetization. A 30-element Ge array X-ray detector has been used to measure the XMCD for these dilute ions, whose concentrations are 1400 ppm for Ni(II) and 10,000 ppm for Mn(II). Large XMCD effects have been observed for both Ni(II) and Mn(II), and multiplet simulation described the observed spectra. The fluorescence-detected L-edge absorption spectrum and XMCD of Ni(II) in MgO are comparable with both theoretical calculations and the total electron yield measured ions in similar chemical environments, at least qualitatively validating the use of the sensitive fluorescence detection technique for studying XMCD for dilute 3d metal ions, such as various metalloproteins. Sum rule analyses on the XMCD spectra are also performed. In addition, these XMCD measurements have also been used to obtain the sample's magnetization curve and the beamline's X-ray helicity curve. This study also illustrated that bend magnet beamlines are still useful in examining XMCD on dilute and paramagnetic metal sites.

  1. Synthesis, crystal structures, molecular docking and urease inhibition studies of Ni(II) and Cu(II) Schiff base complexes

    Science.gov (United States)

    Sangeeta, S.; Ahmad, K.; Noorussabah, N.; Bharti, S.; Mishra, M. K.; Sharma, S. R.; Choudhary, M.

    2018-03-01

    [Ni(L)2] 1 and [Cu(L)2] 2 [HL = 2-((E)-(2-methoxyphenylimino)methyl)-4,6-dichlorophenol] Schiff base complexes have been successfully synthesized and were characterized by FT-IR, UV-Vis, fluorescence spectroscopy and thermogravimetric analysis. The crystal structures of the two complexes were determined through X-ray crystallography. Its inhibitory activity against Helicobacter pylori urease was evaluated in vitro and showed strong inhibitory activity against H. pylori urease compared with acetohydroxamic acid (IC50 = 42.12 μmolL-1), which is a positive reference. A docking analysis using the AutoDock 4.0 program could explain the inhibitory activity of the complex against urease.

  2. Supramolecular structures of Ni(II) and Pt(II) based on the substituted 2, 2‧: 6‧, 2″-terpyridine: Synthesis, structural characterization, luminescence and thermal properties

    Science.gov (United States)

    Momeni, Badri Z.; Rahimi, Farzaneh; Jebraeil, S. Mohammad; Janczak, Jan

    2017-12-01

    Three new d8 transitions metal complexes containing substituted-2,2‧:6‧,2″-terpyridine ligands of [NiII(pytpy)2]Cl2. H2O (pytpy = 4‧- (4-pyridyl)-2,2‧:6‧,2″-terpyridine) (1), [Pt(tpyOH)Cl]+Cl-. 2H2O (2) (tpyOH = 4‧-hydroxy-2,2‧:6‧,2″-terpyridine) and [Pt(tpySH)Cl]+Cl-.2H2O (3) (tpySH = 4‧-mercapto-2,2‧:6‧,2″-terpyridine) have been prepared. The crystal structure of 1 reveals that the nickel(II) is six-coordinated by six nitrogen atoms of pytpy in a distorted octahedral geometry NiN6, while the platinum complex (2) is four-coordinated by one Cl- and three nitrogen atoms of tpyOH in a distorted square planar geometry PtClN3. The lattice crystal water molecule plays a significant structure directing role in the complexes 1 and 2. Many strong noncovalent interactions are present in the crystal structure of 1 and 2. For example, the supramolecular network of Csbnd H⋯Cl, Osbnd H⋯Cl and Cl⋯Cl interactions connected molecules and ions in the crystalline 1, while there are several Pt⋯Pt, Csbnd H⋯Cl, H2O⋯H2O, Csbnd OH⋯H2O, Cl⋯H2O and π-π interactions in 2. The solution luminescence properties of 2 and 3 have been investigated. The emissions of the platinum complexes 2 and 3 exhibit the high-energy intense π→π* intraligand and low-energy MLCT transitions in solution. The solid-state emissions of complexes 1-3 due to the MLCT and π-π interactions are also observed in the solid state. The thermal stability of all complexes reveals that the loss of terpyridine ligand is observed at higher temperatures due to the strong metal-nitrogen bonds of terpyridine ligands.

  3. Critical assessment of the emission spectra of various photosystem II core complexes.

    Science.gov (United States)

    Chen, Jinhai; Kell, Adam; Acharya, Khem; Kupitz, Christopher; Fromme, Petra; Jankowiak, Ryszard

    2015-06-01

    We evaluate low-temperature (low-T) emission spectra of photosystem II core complexes (PSII-cc) previously reported in the literature, which are compared with emission spectra of PSII-cc obtained in this work from spinach and for dissolved PSII crystals from Thermosynechococcus (T.) elongatus. This new spectral dataset is used to interpret data published on membrane PSII (PSII-m) fragments from spinach and Chlamydomonas reinhardtii, as well as PSII-cc from T. vulcanus and intentionally damaged PSII-cc from spinach. This study offers new insight into the assignment of emission spectra reported on PSII-cc from different organisms. Previously reported spectra are also compared with data obtained at different saturation levels of the lowest energy state(s) of spinach and T. elongatus PSII-cc via hole burning in order to provide more insight into emission from bleached and/or photodamaged complexes. We show that typical low-T emission spectra of PSII-cc (with closed RCs), in addition to the 695 nm fluorescence band assigned to the intact CP47 complex (Reppert et al. J Phys Chem B 114:11884-11898, 2010), can be contributed to by several emission bands, depending on sample quality. Possible contributions include (i) a band near 690-691 nm that is largely reversible upon temperature annealing, proving that the band originates from CP47 with a bleached low-energy state near 693 nm (Neupane et al. J Am Chem Soc 132:4214-4229, 2010; Reppert et al. J Phys Chem B 114:11884-11898, 2010); (ii) CP43 emission at 683.3 nm (not at 685 nm, i.e., the F685 band, as reported in the literature) (Dang et al. J Phys Chem B 112:9921-9933, 2008; Reppert et al. J Phys Chem B 112:9934-9947, 2008); (iii) trap emission from destabilized CP47 complexes near 691 nm (FT1) and 685 nm (FT2) (Neupane et al. J Am Chem Soc 132:4214-4229, 2010); and (iv) emission from the RC pigments near 686-687 nm. We suggest that recently reported emission of single PSII-cc complexes from T. elongatus may not represent

  4. Transition probabilities of some Si II lines obtained by laser produced plasma emission

    International Nuclear Information System (INIS)

    Blanco, F.; Botho, B.; Campos, J.

    1995-01-01

    The absolute transition probabilities for 28 Si II spectral lines have been determined by measurement of emission line intensities from laser-produced plasmas of Si in Ar and Kr atmospheres. The studied plasma has a temperature of about 2 . 10 4 K and 10 17 cm -3 electron density. The local thermodynamic equilibrium conditions and plasma homogeneity have been checked. The results are compared with the available experimental and theoretical data and with present Hartree-Fock calculations in LS coupling. (orig.)

  5. Type II successful supernovae, the anatomy of shocks: neutrino emission and the adiabatic index

    International Nuclear Information System (INIS)

    Kahana, S.; Baron, E.; Cooperstein, J.

    1983-01-01

    Hydrodynamic calculations of stellar collapse in Type II Supernova are described using a variable stiffness and compressibility for the nuclear equation of state at high density. Initial models employing a relatively small mass core with low central entropy are necessary to achieve viable shocks; near success the models are sensitive to both neutrino emission and the high density equation of state. The treatment of neutrino production and transport is sketched and recent results reported

  6. Clinical Imaging Characteristics of the Positron Emission Mammography Camera: PEM Flex Solo II

    OpenAIRE

    MacDonald, Lawrence; Edwards, John; Lewellen, Thomas; Haseley, David; Rogers, James; Kinahan, Paul

    2009-01-01

    We evaluated a commercial positron emission mammography (PEM) camera, the PEM Flex Solo II. This system comprises two 6 × 16.4 cm detectors that scan together covering up to a 24 × 16.4 cm field of view (FOV). There are no specific standards for testing this detector configuration. We performed several tests important to breast imaging, and we propose tests that should be included in standardized testing of PEM systems.

  7. Beta-delayed gamma and neutron emission near the double shell closure at 78Ni

    International Nuclear Information System (INIS)

    Rykaczewski, Krzysztof Piotr; Mazzocchi, C.; Grzywacz, R.; Batchelder, J. C.; Bingham, C.R.; Fong, D.; Hamilton, J.H.; Hwang, J.K.; Karny, M.; Krolas, W.; Liddick, S. N.; Morton, A. C.; Mantica, P. F.; Mueller, W. F.; Steiner, M.; Stolz, A.; Winger, J.A.

    2005-01-01

    An experiment was performed at the National Superconducting Cyclotron Laboratory at Michigan State University to investigate β decay of very neutron-rich cobalt isotopes. Beta-delayed neutron emission from 71-74 Co has been observed for the first time. Preliminary results are reported

  8. Assessing comparative terrestrial ecotoxicity of Cd, Co, Cu, Ni, Pb, and Zn: The influence of aging and emission source

    International Nuclear Information System (INIS)

    Owsianiak, Mikołaj; Holm, Peter E.; Fantke, Peter; Christiansen, Karen S.; Borggaard, Ole K.; Hauschild, Michael Z.

    2015-01-01

    Metal exposure to terrestrial organisms is influenced by the reactivity of the solid-phase metal pool. This reactivity is thought to depend on the type of emission source, on aging mechanisms that are active in the soil, and on ambient conditions. Our work shows, that when controlling for soil pH or soil organic carbon, emission source occasionally has an effect on reactivity of Cd, Co, Cu, Ni, Pb and Zn emitted from various anthropogenic sources followed by aging in the soil from a few years to two centuries. The uncertainties in estimating the age prevent definitive conclusions about the influence of aging time on the reactivity of metals from anthropogenic sources in soils. Thus, for calculating comparative toxicity potentials of man-made metal contaminations in soils, we recommend using time-horizon independent accessibility factors derived from source-specific reactive fractions. - Highlights: • We found an effect of source on reactivity of anthropogenic metals in soils. • The influence of aging on reactivity of anthropogenic metals was not consistent. • We recommend including source and disregarding aging in calculation of CTPs values. - Improving current life cycle inventory (LCI) and life cycle impact assessment (LCIA) practice in terrestrial ecotoxicity assessment of metals.

  9. A First Comparison of Millimeter Continuum and Mg ii Ultraviolet Line Emission from the Solar Chromosphere

    Energy Technology Data Exchange (ETDEWEB)

    Bastian, T. S. [National Radio Astronomy Observatory, 520 Edgemont Road, Charlottesville, VA 22903 (United States); Chintzoglou, G.; De Pontieu, B.; Schmit, D. [Lockheed Martin Solar and Astrophysics Lab, Org. A021S, Building 252, 3251 Hanover Street, Palo Alto, CA 94304 (United States); Shimojo, M. [National Astronomical Observatory of Japan, 2-21-1, Osawa, Mitaka, Tokyo 181-8588 (Japan); Leenaarts, J. [Institute for Solar Physics, Department of Astronomy, Stockholm University, AlbaNova University Centre, SE-106 91 Stockholm (Sweden); Loukitcheva, M., E-mail: tbastian@nrao.edu [Center For Solar-Terrestrial Research, New Jersey Institute of Technology, 323 Martin Luther King Boulevard, Newark, NJ 07102 (United States)

    2017-08-20

    We present joint observations of the Sun by the Atacama Large Millimeter/submillimeter Array (ALMA) and the Interface Region Imaging Spectrograph ( IRIS ). Both millimeter/submillimeter- λ continuum emission and ultraviolet (UV) line emission originate from the solar chromosphere and both have the potential to serve as powerful and complementary diagnostics of physical conditions in this enigmatic region of the solar atmosphere. The observations were made of a solar active region on 2015 December 18 as part of the ALMA science verification effort. A map of the Sun’s continuum emission was obtained by ALMA at a wavelength of 1.25 mm (239 GHz). A contemporaneous map was obtained by IRIS in the Mg ii h doublet line at 2803.5 Å. While a clear correlation between the 1.25 mm brightness temperature T{sub B} and the Mg ii h line radiation temperature T {sub rad} is observed, the slope is <1, perhaps as a result of the fact that these diagnostics are sensitive to different parts of the chromosphere and that the Mg ii h line source function includes a scattering component. There is a significant difference (35%) between the mean T{sub B} (1.25 mm) and mean T {sub rad} (Mg ii). Partitioning the maps into “sunspot,” “quiet areas,” and “plage regions” we find the relation between the IRIS Mg ii h line T {sub rad} and the ALMA T {sub B} region-dependent. We suggest this may be the result of regional dependences of the formation heights of the IRIS and ALMA diagnostics and/or the increased degree of coupling between the UV source function and the local gas temperature in the hotter, denser gas in plage regions.

  10. Terahertz Emission of Ferromagnetic Ni-Fe Thin Films Excited by Ultrafast Laser Pulses

    International Nuclear Information System (INIS)

    Shen Jian; Zhang Huai-Wu; Li Yuan-Xun

    2012-01-01

    It is believed that the ultrafast demagnetization process in ferromagnetic film is intrinsically a thermal effect, which is induced by ultrafast laser pulses. We present experimental evidence that such ultrafast demagnetization of the NiFe thin film can radiate electromagnetic waves in the terahertz range. We also demonstrate that the magnitude of the terahertz electromagnetic pulse emitted from ferromagnetic films after pulsed laser excitation can be tuned by the Gilbert damping factor α, which is conventionally used to describe damping of GHz precession motion of magnetization. Different damping factors are obtained by varying the normal metal film adjacent to the magnetic film via spin pumping. The measured radiated electric field in the far field is found to be proportional to the Gilbert damping factor. (condensed matter: electronic structure, electrical, magnetic, and optical properties)

  11. Coordination versatility of N2O4 polydentate hydrazonic ligand in Zn(II, Cu(II, Ni(II, Co(II, Mn(II and Pd(II complexes and antimicrobial evaluation

    Directory of Open Access Journals (Sweden)

    Fathy A. El-Saied

    2017-12-01

    Full Text Available New polydentate hydrazone ligand, was synthesized by the condensation of 1,5-dimethyl-3-oxo-2-phenylpyrazole-4-carbaldehyde with adipodihydrazide. The structure of the synthesized ligand, N′1,N′6-bis((1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl methylene adipohydrazide was elucidated by various analytical and spectroscopic techniques. The reactions of the ligand with zinc(II, copper(II, nickel(II, cobalt(II, manganese(II and palladium(II salts afforded homobinuclear metal complexes. Characterization and structure elucidation of the prepared complexes were achieved using different analytical and spectroscopic techniques. The analyses data indicated that this ligand behaved as N2O4 dibasic hexadentate ligand bonded covalency to the metal ions through the enolic carbonyl oxygen of hydrazide moiety and coordinated via carbonyl oxygen of antipyrine moiety and azomethine nitrogen atoms forming distorted octahedral geometry around the metal ions. The ESR spectra of copper(II complexes (3 and (4 showed an axial symmetry with g||>g⊥>ge, indicating distorted octahedral structure and presence of the unpaired electron in d(x2−y2 orbital. The microbicide studies of the ligand and its metal complexes (2, (3, (4, (5, (8, (11 and (13 showed that, all these complexes exhibit moderate to mild inhibitory effects on B. subtilis, E. coli while complexes (2, (3, (4 and (13 exhibit moderate to mild inhibitory effects on A. niger. Keywords: Hexadentate, Hydrazone, Antipyrine, ESR, Adipohydrazide, Microbicide

  12. The Relationship between Mg ii Broad Emission and Quasar Inclination Angle

    Energy Technology Data Exchange (ETDEWEB)

    Wildy, Conor; Czerny, Bozena, E-mail: wildy@cft.edu.pl [Center for Theoretical Physics, Polish Academy of Sciences, Warsaw (Poland)

    2017-11-14

    Several observed spectral properties of quasars are believed to be influenced by quasar orientation. In this investigation we examine the effect of orientation on the Mg ii line located at 2,798 Å in a sample of 36 radio-loud quasars, with orientation angles having been obtained in a previous study using radio observations. We find no significant relationship between orientation angle and either Mg ii line full-width at half-maximum or equivalent width. The lack of correlation with inclination angle contradicts previous studies which also use radio data as a proxy for inclination angle and suggests the Mg ii emission region does not occupy a disk-like geometry. The lack of correlation with Mg ii equivalent width, however, is reported in at least one previous study. Although the significance is not very strong (86%), there is a possible negative relationship between inclination angle and Fe ii strength which, if true, could explain the Fe ii anti-correlation with [O iii] strength associated with Eigenvector 1. Interestingly, there are objects having almost edge-on inclinations while still exhibiting broad lines. This could be explained by a torus which is either clumpy (allowing sight lines to the central engine) or mis-aligned with the accretion disk.

  13. The Relationship between Mg ii Broad Emission and Quasar Inclination Angle

    Directory of Open Access Journals (Sweden)

    Conor Wildy

    2017-11-01

    Full Text Available Several observed spectral properties of quasars are believed to be influenced by quasar orientation. In this investigation we examine the effect of orientation on the Mg ii line located at 2,798 Å in a sample of 36 radio-loud quasars, with orientation angles having been obtained in a previous study using radio observations. We find no significant relationship between orientation angle and either Mg ii line full-width at half-maximum or equivalent width. The lack of correlation with inclination angle contradicts previous studies which also use radio data as a proxy for inclination angle and suggests the Mg ii emission region does not occupy a disk-like geometry. The lack of correlation with Mg ii equivalent width, however, is reported in at least one previous study. Although the significance is not very strong (86%, there is a possible negative relationship between inclination angle and Fe ii strength which, if true, could explain the Fe ii anti-correlation with [O iii] strength associated with Eigenvector 1. Interestingly, there are objects having almost edge-on inclinations while still exhibiting broad lines. This could be explained by a torus which is either clumpy (allowing sight lines to the central engine or mis-aligned with the accretion disk.

  14. Flexible porous coordination polymer of Ni(II) for developing nanoparticles through acid formation and redox activity of the framework

    Science.gov (United States)

    Agarwal, Rashmi A.

    2017-10-01

    Immobilization of the nanoparticles (NPs) in a two dimensional porous coordination polymer (PCP) is currently an emerging field for a number of applications. But still it is a great challenge to fabricate any specified metal NPs in a single network. Herein the synthesis of Au, Pd, Mn, Fe, Cu, Zn, Mg, Li, Fe/Cu, Zn/Mg etc, NPs in a highly flexible PCP of Ni(II); {[Ni3(TBIB)2(BTC)2(H2O)6]·5C2H5OH·9H2O}n [TBIB = 1,3,5-tri(1H-benzo[d]imidazol-1-yl)benzene, H3BTC = 1,3,5-benzenetricarboxylic acid] have been reported. This universal host is able to grow mixed metal NPs from mixed metal precursors. Monodentate carboxylate groups of BTC linker act as anchoring sites for the metal ions of the metal precursors. This is the main driving force to grow NPs within the cavities along with the high flexibility of this polymer at room temperature. Mechanism involves acid formation followed by redox reaction to synthesize metal NPs explained by EPR and FTIR. Paramagnetic properties have been shown by as-synthesized Fe NPs integrated framework at room temperature under applied magnetic field up to 17,500 Oe.

  15. Two new Ni(II) Schiff base complexes : X-ray absolute structure determination, synthesis of a N-15-labelled complex and full assignment of its H-1 NMR and C-13 NMR spectra

    NARCIS (Netherlands)

    Langer, Vratislav; Popkov, Alexander; Nadvornik, Milan; Lycka, Antonin

    2007-01-01

    The Ni(II) complex of the Schiff base of (S)-N-(2-benzoyl-4-chlorophenyl)-1-benzylpyrrolidine-2-carboxamide and glycine (1) [GKCI] and the hemihydrate of the Ni(II) complex of the Schiff base of (S)-N-(2-benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide and 2-aminoisobutiric acid (2) Me(2)GK] were

  16. The n-propyl 3-azido-2,3-dideoxy-β-D-arabino-hexopyranoside: Syntheses, crystal structure, physical properties and stability constants of their complexes with Cu(II), Ni(II) and VO(II)

    Science.gov (United States)

    Barabaś, Anna; Madura, Izabela D.; Marek, Paulina H.; Dąbrowska, Aleksandra M.

    2017-11-01

    The structure, conformation and configuration of the n-propyl 3-azido-2,3-dideoxy-β-D-arabino-hexopyranoside (BAra-nPr) were determined by 1H NMR, 13C NMR, and IR spectroscopy, as well as by optical rotation. The crystal structure was confirmed by single-crystal X-ray diffraction studies at room temperature. The compound crystallizes in P21 space group symmetry of the monoclinic system. The molecule has a 4C1 chair conformation with azide group in the equatorial position both in a solution as well as in the crystal. The spatial arrangement of azide group is compared to other previously determined azidosugars. The hydrogen bonds between the hydroxyl group of sugar molecules lead to a ribbon structure observed also for the ethyl homolog. The packing of ribbons is dependent on the alkyl substituent length and with the elongation changes from pseudohexagonal to lamellar. Acidity constants for the n-propyl 3-azido-2,3-dideoxy-β-D-arabino-hexopyranoside (BAra-nPr) in an aqueous solution were evaluated by the spectrophotometric and potentiometric titrations methods. Title compound exhibit blue absorption with the maximum wavelengths in the range of 266 nm and 306 nm. Based on these measurements we showed equilibria existing in a particular solution and a distribution of species which have formed during the titration. We also investigated interactions between Cu(II), Ni(II) and VO(II) and title compound (as ligand L) during complexometric titration. On these bases we identified that in [CuII-BAra-nPr]2+ the ratio of the ligand L to metal ion M(II) was 3:1, while in [NiII-BAra-nPr]2+ and [VOII-BAra-nPr]2+ complexes 2:1 ratios were found. The cumulative stability constants (as log β) occurring in an aqueous solution for the complexes of BAra-nPr with Cu(II), Ni(II) and VO(IV) were 14.57; 11.71 and 4.20, respectively.

  17. SYNTHESE D’EXTRACTANTS ACIDES HEXADECYL- ET DECYLAMINOBIMETHYLENEDIPHOSPHONIQUES APPLICATION A L’EXTRACTION LIQUIDE-LIQUIDE DE Ni (II

    Directory of Open Access Journals (Sweden)

    M.A DIDI

    2007-06-01

    Après purification puis caractérisation des produits, nous avons réalisé divers tests d’extraction liquide - liquide de Ni (II en milieu sulfaté. Le temps d’équilibre déterminé par étude cinétique a été fixé à 40 minutes. Les paramètres changeant tels la température ( T = 20°C, 30°C et 50°C, le rapport du nombre de moles (n extractant / n métal (Q =1 à 6 et le rapport des volumes (Vaq / Vorg= 1, 2, 3 et 4 ont permis de maximiser le rendement d’extraction qui est de 46% avec le HABMP et de 44% pour le DADMP et ceci pour des extractions à un seul plateau.

  18. Removal of Ni(II from aqueous solution using leaf, bark and seed of Moringa stenopetala adsorbents

    Directory of Open Access Journals (Sweden)

    A. A. Mengistie

    2013-04-01

    Full Text Available The present study investigates the possibility of using leaf, bark and seed of Moringa stenopetala as alternative adsorbents for removal of Ni(II from aqueous solutions. The optimum adsorption conditions for removal of Ni(II were found to be 30, 20 and 50 mg/L initial concentration, 1.5, 2 and 2.5 g adsorbent dose, 250, 250 and 300 rpm agitation speed, 90, 120 and 90 min contact time, 40, 30 and 23 oC temperature and pH of 5, 6 and 6 using leaf, bark and seed as adsorbent, respectively. At optimum experimental conditions the percent adsorption of synthetic wastewater sample was found to be 93.90, 96.25 and 97.50 for leaf, bark and seed, respectively. The tested experimental data best fits to pseudo-second order (R2 > 0.98 than pseudo-first order, Elovich and intraparticle diffusion kinetic models indicating rate limiting step to be chemisorption. It also fits to Langmuir (R2 > 0.895 using adsorbate variation and also R2 > 0.998 using both time and temperature variation data than Freundlich, Temkin and D-R isotherm models. D-R isotherm and thermodynamic study reveals formation of physical adsorption. Hence the adsorption mechanism could be regarded as physico-chemical adsorption process. The adsorption results of industrial wastewater also reveal that for removal of nickel 83% and 85% was obtained using bark and seed adsorbents, respectively. The new method of adsorption developed in this study is cheap, fast and environmental friendly.DOI: http://dx.doi.org/10.4314/bcse.v27i1.4

  19. Search for high energy γ-rays emission in 28Si, 32Si+64Ni dissipative reactions at about 5 MeV/amu incident energy

    International Nuclear Information System (INIS)

    Agodi, C.; Alba, R.; Anzalone, A.; Coniglione, R.; Zoppo, A. del; Finocchiaro, P.; Maiolino, C.; Papa, M.; Piattelli, P.; Sapienza, P.; Wang, Q.; DeRosa, A.; Fioretto, E.; Inglima, G.; Romoli, M.; Sandoli, M.

    1991-01-01

    Photons emitted in the 28 Si+ 64 Ni and 32 S+ 64 Ni reactions at 143 MeV and 156 MeV incident energy respectively, have been detected in coincidence with the ejected charged fragments. An array of 48 BaF 2 γ-rays detector and 6 solid state silicon detector telescopes have been used. Photon energy spectra measured in the energy range from 2 to 20 MeV in coincidence with ejectiles coming from deep inelastic reactions, are consistent with statistical emission from the reaction products. (orig.)

  20. Search for high energy. gamma. -rays emission in sup 28 Si, sup 32 Si+ sup 64 Ni dissipative reactions at about 5 MeV/amu incident energy

    Energy Technology Data Exchange (ETDEWEB)

    Agodi, C.; Alba, R.; Anzalone, A.; Coniglione, R.; Zoppo, A. del; Finocchiaro, P.; Maiolino, C.; Papa, M.; Piattelli, P.; Sapienza, P.; Wang, Q. (Istituto Nazionale di Fisica Nucleare, Catania (Italy). Lab. Nazionale del Sud); Bellia, G.; Cavallaro, S.; Migneco, E.; Pappalardo, G.; Rizzo, F.; Russo, G. (Catania Univ. (Italy). Dipt. di Fisica Istituto Nazionale di Fisica Nucleare, Catania (Italy). Lab. Nazionale del Sud); Cardella, G.; Wang, G.S. (Istituto Nazionale di Fisica Nucleare, Catania (Italy)); DeRosa, A.; Fioretto, E.; Inglima, G.; Romoli, M.; Sandoli, M. (Naples-2 Univ. (Italy). Dipt. di Scienze Fisiche Istituto Nazionale di Fisica Nucleare, Naples (Italy))

    1991-11-01

    Photons emitted in the {sup 28}Si+{sup 64}Ni and {sup 32}S+{sup 64}Ni reactions at 143 MeV and 156 MeV incident energy respectively, have been detected in coincidence with the ejected charged fragments. An array of 48 BaF{sub 2} {gamma}-rays detector and 6 solid state silicon detector telescopes have been used. Photon energy spectra measured in the energy range from 2 to 20 MeV in coincidence with ejectiles coming from deep inelastic reactions, are consistent with statistical emission from the reaction products. (orig.).

  1. Synthesis and Characterization of 2-(Hydroxyimino-1-(phenylpropylidenethiocarbonohydrazide and its Metal Complexes with Co(II, Ni(II and Cu(II Ions

    Directory of Open Access Journals (Sweden)

    A. Venkatchallam

    2009-01-01

    Full Text Available Synthesis and characterization of 2-(hydroxyimino-1-(phenyl propylidene thiocarbonohydrazide (called ‘HPTCHOPD’ was studied. The synthesized compound having the molecular formula C10H13N5OS, where in isonitrosopropiophenone is reacted with thiocarbonohydrazide in presence of sodium acetate in ethanol-water mixture. The yield which is comprises effecting the reaction in the presence of sodium acetate. Also the present work report a process for producing metal complexes having the formula ML2 and (ML2 Cl, wherein M is the divalent metal cation, like cobalt (Co+2, nickel (Ni+2 and copper (Cu+2. The compound HPTCHOPD is admixed with a basic divalent compound that is halide, mainly chloride of Co+2, Ni+2 and Cu+2 in presence of methanol-water mixture. The metal complexes so produced are characterized on the basis of spectral, elemental and magnetic analysis; reveal interesting geometries and bonding features. The data suggested square planar geometry for Co+2 complex, a distorted tetrahedral/square planar-octahedral geometry for Ni+2 complex and a bridged structure for Cu+2 complex.

  2. Incorporation of Ni(II)-dimethylglyoxime ion-imprinted polymer into ...

    African Journals Online (AJOL)

    2011-02-03

    Feb 3, 2011 ... REDDY MRP (2004) Multielement determination in gum opium by microwave digestion and inductively coupled plasma optical emission spectroscopy. Chem. Pap. 58 (2) 101-103. SHAO X, HU S and GOVIND R (1991) Continuous membrane dialysis using ion-exchange resin suspension for extracting ...

  3. New discrete and polymeric supramolecular architectures derived from dinuclear Co(II), Ni(II) and Cu(II) complexes of aryl-linked bis-beta-diketonato ligands and nitrogen bases: synthetic, structural and high pressure studies.

    Science.gov (United States)

    Clegg, Jack K; Hayter, Michael J; Jolliffe, Katrina A; Lindoy, Leonard F; McMurtrie, John C; Meehan, George V; Neville, Suzanne M; Parsons, Simon; Tasker, Peter A; Turner, Peter; White, Fraser J

    2010-03-21

    New examples of nitrogen base adducts of dinuclear Co(II), Ni(II) and Cu(II) complexes of the doubly deprotonated forms of 1,3-aryl linked bis-beta-diketones of type [RC(=O)CH(2)C(=O)C(6)H(4)C(=O)CH(2)C(=O)R] (L(1)H(2)) incorporating the mono- and difunctional amine bases pyridine (Py), 4-ethylpyridine (EtPy), piperidine (pipi), 1,4-piperazine (pip), N-methylmorpholine (mmorph), 1,4-dimethylpiperazine (dmpip) and N,N,N',N'-tetramethylethylenediamine (tmen) have been synthesised by reaction of the previously reported [Cu(2)(L(1))(2)].2.5THF (R = Me), [Cu(2)(L(1))(2)(THF)(2)] (R = t-Bu), [Ni(2)(L(1))(2)(Py)(4)] (R = t-Bu) and [Co(2)(L(1))(2)(Py)(4)] (R = t-Bu) complexes with individual bases of the above type. Comparative X-ray structural studies involving all ten base adduct derivatives have been obtained and reveal a range of interesting discrete and polymeric molecular architectures. The respective products have the following stoichiometries: [Cu(2)(L(1))(2)(Py)(2)].Py (R = Me), [Cu(2)(L(1))(2)(EtPy)(2)].2EtPy (R = t-Bu), [Cu(2)(L(1))(2)(pipi)(2)].2pipi (R = t-Bu), [Cu(2)(L(1))(2)(mmorph)(2)] (R = t-Bu), [Cu(2)(L(1))(2)(tmen)(2)] (R = t-Bu) and {[Cu(2)(L(1))(2)(pip)].pip.2THF}(n), [Co(2)(L(1))(2)(tmen)(2)] (R = t-Bu), [Ni(2)(L(1))(2)(Py)(4)].dmpip (R = t-Bu), [Ni(2)(L(1))(2)(pipi)(4)].pipi (R = t-Bu) and [Ni(2)(L(1))(2)(tmen)(2)] (R = t-Bu). The effect of pressure on the X-ray structure of [Cu(2)(L(1))(2)(mmorph)(2)] has been investigated. An increase in pressure from ambient to 9.1 kbar resulted in modest changes to the unit cell parameters as well as a corresponding decrease of 6.7 percent in the unit cell volume. While a small 'shearing' motion occurs between adjacent molecular units throughout the lattice, no existing bonds are broken or new bonds formed.

  4. Emission Spectroscopy as a Probe into Photoinduced Intramolecular Electron Transfer in Polyazine Bridged Ru(II,Rh(III Supramolecular Complexes

    Directory of Open Access Journals (Sweden)

    Karen J. Brewer

    2010-08-01

    Full Text Available Steady-state and time-resolved emission spectroscopy are valuable tools to probe photochemical processes of metal-ligand, coordination complexes. Ru(II polyazine light absorbers are efficient light harvesters absorbing in the UV and visible with emissive 3MLCT excited states known to undergo excited state energy and electron transfer. Changes in emission intensity, energy or band-shape, as well as excited state lifetime, provide insight into excited state dynamics. Photophysical processes such as intramolecular electron transfer between electron donor and electron acceptor sub-units may be investigated using these methods. This review investigates the use of steady-state and time-resolved emission spectroscopy to measure excited state intramolecular electron transfer in polyazine bridged Ru(II,Rh(III supramolecular complexes. Intramolecular electron transfer in these systems provides for conversion of the emissive 3MLCT (metal-to-ligand charge transfer excited state to a non-emissive, but potentially photoreactive, 3MMCT (metal-to-metal charge transfer excited state. The details of the photophysics of Ru(II,Rh(III and Ru(II,Rh(III,Ru(II systems as probed by steady-state and time-resolved emission spectroscopy will be highlighted.

  5. Modelling of the Ni(II) removal from aqueous solutions onto grape stalk wastes in fixed-bed column.

    Science.gov (United States)

    Valderrama, César; Arévalo, Jaime A; Casas, Ignasi; Martínez, María; Miralles, Nuria; Florido, Antonio

    2010-02-15

    Grape stalk wastes generated in the wine production process were used for the removal of nickel (II) from aqueous solution. The experimental breakthrough curves were obtained in fixed-bed columns. Experiments we carry out in order to evaluate the influence of inlet metal concentration (30 and 70 mg L(-1)) and the regeneration process in a double sorption cycle. The CXTFIT code was used to fit the experimental data and to determine the transport and sorption parameters of the convective-dispersive equation (CDE) and the two-site deterministic non-equilibrium (TSM/CDE) model by adjusting the models to the experimental breakthrough curves (BTC). The results showed that bed capacity as well as transport and sorption parameters were affected by the initial metal concentration, at the highest Ni(II) concentration the grape stalks column saturated quickly leading to earlier breakthrough. The sorption capacity of the sorbent was slightly reduced in a double sorption cycle, while the recovery of the metal in the desorption step was ranging between 80% and 85% in both cycles.

  6. Simultaneous investigation of thermal, acoustic, and magnetic emission during martensitic transformation in single-crystalline Ni2MnGa

    Science.gov (United States)

    Tóth, László Z.; Daróczi, Lajos; Szabó, Sándor; Beke, Dezső L.

    2016-04-01

    Simultaneous thermal, acoustic, and magnetic emission (AE and ME) measurements during thermally induced martensitic transformation in Ni2MnGa single crystals demonstrate that all three types of the above noises display many coincident peaks and the same start and finish temperatures. The amplitude and energy distribution functions for AE and ME avalanches satisfy power-law behavior, corresponding to the symmetry of the martensite. At zero external magnetic field asymmetry in the exponents was obtained: their value was larger for heating than for cooling. Application of constant, external magnetic fields (up to B =722 mT) leads to the disappearance of the above asymmetry, due to the decrease of the multiplicity of the martensite variants. Time correlations (i.e., the existence of nonhomogeneous temporal processes) within AE as well as ME emission events are demonstrated by deviations from the uncorrelated behavior on probability distributions of waiting times as well as of a sequence of number of events. It is shown that the above functions collapse on universal master curves for cooling and heating as well as for AE and ME noises. The analysis of the existence of temporal correlations between AE and ME events revealed that at short times the acoustic signals show a time delay relative to the magnetic one, due to the time necessary for the propagation of the ultrasound. At intermediate times, as expected, the magnetic signal is delayed, i.e., the magnetic domain rearrangement followed the steps of structural transformation. At much longer times the deviation from an uncorrelated (Poisson-type) behavior is attributed to the nonhomogeneity of the avalanche statistics.

  7. Synthesis and Crystal Structures of Ni(II)/(III) and Zn(II) Complexes with Schiff Base Ligands

    International Nuclear Information System (INIS)

    Koo, Bon Kweon

    2013-01-01

    Coordination polymers are of great interest due to their intriguing structural motifs and potential applications in optical, electronic, magnetic, and porous materials. The most commonly used strategy for designing such materials relies on the utilization of multidentate N- or Odonor ligands which have the capacity to bridge between metal centers to form polymeric structures. The Schiff bases with N,O,S donor atoms are an useful source as they are readily available and easily form stable complexes with most transition metal ions. Schiff bases are also important intermediates in synthesis of some bioactive compounds and are potent anti-bacterial, anti-fungal, anticancer and antiviral compounds. In this work, the Schiff bases, Hapb and Hbpb, derived from 2-acetylpyridene or 2-benzoylpyridine and benzhydrazide were taken as trifunctional (N,N,O) monobasic ligand (Scheme 1). This ligand is of important because the π-delocalization of charge and the configurational flexibility of their molecular chain can give rise to a great variety of coordination modes. Although many metal.Schiff base complexes have been reported, the 1D, 2D, and 3D networks of coordination polymers linked through the bridging of ligands such as dicyanamide, N(CN) 2 - as coligand have been little published. In the process of working to extend the dimensionality of the metal-Schiff base complexes using benzilic acid as a bridging ligand, we obtained three simple metal (II)/(III) complexes of acetylpyridine/2-benzoyl pyridine based benzhydrazide ligand. Therefore, we report here the synthesis and crystal structures of the complexes

  8. Synthesis and Crystal Structures of Ni(II)/(III) and Zn(II) Complexes with Schiff Base Ligands

    Energy Technology Data Exchange (ETDEWEB)

    Koo, Bon Kweon [Catholic Univ., of Daegu, Daegu (Korea, Republic of)

    2013-12-15

    Coordination polymers are of great interest due to their intriguing structural motifs and potential applications in optical, electronic, magnetic, and porous materials. The most commonly used strategy for designing such materials relies on the utilization of multidentate N- or Odonor ligands which have the capacity to bridge between metal centers to form polymeric structures. The Schiff bases with N,O,S donor atoms are an useful source as they are readily available and easily form stable complexes with most transition metal ions. Schiff bases are also important intermediates in synthesis of some bioactive compounds and are potent anti-bacterial, anti-fungal, anticancer and antiviral compounds. In this work, the Schiff bases, Hapb and Hbpb, derived from 2-acetylpyridene or 2-benzoylpyridine and benzhydrazide were taken as trifunctional (N,N,O) monobasic ligand (Scheme 1). This ligand is of important because the π-delocalization of charge and the configurational flexibility of their molecular chain can give rise to a great variety of coordination modes. Although many metal.Schiff base complexes have been reported, the 1D, 2D, and 3D networks of coordination polymers linked through the bridging of ligands such as dicyanamide, N(CN){sub 2}{sup -} as coligand have been little published. In the process of working to extend the dimensionality of the metal-Schiff base complexes using benzilic acid as a bridging ligand, we obtained three simple metal (II)/(III) complexes of acetylpyridine/2-benzoyl pyridine based benzhydrazide ligand. Therefore, we report here the synthesis and crystal structures of the complexes.

  9. Remote sensing CO, CO II in vehicle emissions based on TDLAS

    Science.gov (United States)

    Wang, Tiedong; Liu, Wenqing; Zhang, Yujun; Liu, Jianguo; Dong, Fengzhong; Wang, Min; Wang, Xiaomei; Xu, Min

    2006-06-01

    Knowing the quantity of pollutants that the vehicle fleet is emitting to the air has become a vital question in almost every major city in China. Finding and fixing gross polluters is therefore very important to control the urban air quality and protect the human health and the environment. Remote sensing is an important advance in the technology of on-road vehicle emissions testing because it is fast, mobile, and unobtrusive. This on-road vehicle emissions remote system is designed to measure the carbon monoxide, carbon dioxide and opacity from the vehicles's tailpipe based on the Tuneable Diode Laser Absorption Spectroscopy (TDLAS). There are several advantages of this system such as compact design and ease of use. The measurement principle and optical layout of the instrument has been described in this paper. Field testing at Beijing and Hefei were conducted over one year, more than 6000 vehicles were tested. This vehicle emissions remote system has been shown to be able to measure CO,CO II and opacity from individual at highway speeds. In parallel, the plate license, speed, acceleration and length of vehicle are recognised by computer so that the owners of vehicles exceeding the permissible level of emissions can be identified.

  10. Characteristics of equilibrium, kinetics studies for adsorption of Hg(II), Cu(II), and Ni(II) ions by thiourea-modified magnetic chitosan microspheres

    International Nuclear Information System (INIS)

    Zhou Limin; Wang Yiping; Liu Zhirong; Huang Qunwu

    2009-01-01

    Magnetic chitosan microspheres were prepared and chemically modified with thiourea (TMCS) for adsorption of metal ions. TMCS obtained were investigated by means of X-ray diffraction (XRD), IR, magnetic properties and thermogravimetric analysis (TGA). The adsorption properties of TMCS toward Hg 2+ , Cu 2+ , and Ni 2+ ions were evaluated. Various factors affecting the uptake behavior such as contact time, temperature, pH and initial concentration of the metal ions were investigated. The kinetics was evaluated utilizing the pseudo-first-order, pseudo-second-order, and the intra-particle diffusion models. The equilibrium data were analyzed using the Langmuir, Freundlich, and Tempkin isotherm models. The adsorption kinetics followed the mechanism of the pseudo-second-order equation for all systems studied, evidencing chemical sorption as the rate-limiting step of adsorption mechanism and not involving a mass transfer in solution. The best interpretation for the equilibrium data was given by Langmuir isotherm, and the maximum adsorption capacities were 625.2, 66.7, and 15.3 mg/g for Hg 2+ , Cu 2+ , and Ni 2+ ions, respectively. TMCS displayed higher adsorption capacity for Hg 2+ in all pH ranges studied. The adsorption capacity of the metal ions decreased with increasing temperature. The metal ion-loaded TMCS with were regenerated with an efficiency of greater than 88% using 0.01-0.1 M ethylendiamine tetraacetic acid (EDTA)

  11. Biomass assisted synthesis of alumina by Gardenia Jasminoides Ellis and their application for removal of Ni(II) from aqueous solution

    International Nuclear Information System (INIS)

    Zheng, Nan; Zhao, Yusheng; Song, Qianqian; Jia, Lishan; Fang, Weiping

    2013-01-01

    Highlights: • A simple process has been proposed to synthesis alumina using biomass. • The absorbent with biomass is highly effective for the adsorption of Ni 2+ . • Three adsorption–desorption cycles showed that the adsorbent was basically stable. -- Abstract: A simple and novel process has been proposed to synthesize alumina using gardenia extract and aluminum salts in an aqueous solution. The alumina sample notated as “bio-Al 2 O 3 ” was characterized by X-ray diffraction (XRD) and nitrogen adsorption–desorption experiment. The results indicated that the existence of the gardenia biomass enlarged the surface area of alumina and reached 256 m 2 /g. The thermo gravimetric (TG), X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared (FTIR) results showed that gardenia biomass bound to the surface of the alumina has substantially improved the adsorption capacity of Ni(II) and the adsorption behavior of nickel ion was related to the biomass functional groups. The results of three adsorption–desorption cycles showed that the bio-Al 2 O 3 using as the adsorbent for Ni(II) was relatively stable. The kinetic of the Ni(II) adsorption by the bio-Al 2 O 3 followed pseudo-second-order equation. Langmuir and Freundlich isotherm models were applied to analyze the experimental data and the result demonstrated that the adsorption isotherms followed Langmuir isotherm model

  12. Adsorption of NI (II on activated Carbon of Coconut shell Chemicaly Modifieded with Acid Nitric Solutions

    Directory of Open Access Journals (Sweden)

    Mónica Hernández-Rodríguez

    2017-01-01

    Full Text Available In the research the effect of modification of coconut shell activated carbon with diluted solutions of nitric acid, in its chemical characteristics and removal capacity of the nickel (II ions present in modeling solutions of sulfates with similar characteristics to the acid liquor waste of the nickel industry, was studied. The characterization of the adsorbent material evidenced that the modification process increases the superficial acids groups according with the increase of acid nitric concentration employee in the treatment. The adsorption equilibrium tests, carried out with metallic species solutions at concentrations between 0,5 and 3,5 g/L evidenced that the process is described by Freundlich model. The effect of chemical modification of the adsorbent material in adsorption capacity of nickel (II ions was evaluated using a traditional experimental design at pH of 1,2 and 6,9 units, obtaining that the increase of acid groups in the carbon surface causes an increase of adsorption capacity and removal percentages of nickel (II, due to specific interactions of these groups with the metal cations.

  13. Emission-Line Studies of Young Stars. II. The Herbig Ae/Be Stars

    Science.gov (United States)

    Hamann, Fred; Persson, S. E.

    1992-09-01

    We present optical emission-line data for a sample of 32 Herbig Ae/Be stars. Many of the Herbig stars have line spectra similar to the "classical" (strong Hα) T Tauri stars. The Herbig stars with the most T Tauri-like characteristics are the ones that also have direct evidence for outflow in their spectra, e.g., P Cygni profiles or broad or blueshifted forbidden lines. Among the similarities derived from the Ca II triplet lines are space densities of ≳1011-3, column densities of Nβ ≳ 1021 cm-3, and optically thick emitting areas that can be several times larger than the stars. The triplet line profiles also suggest similar dynamical environments. Some Herbig stars have the distinctive Ca II triplet signature observed in the T Tauri stars, where 8498 Å has the largest peak height but the narrowest width of the three. We interpret this in terms of increasing velocities and decreasing triplet source functions outward through the emitting gas. Based on these similarities we suggest that the models developed for classical T Tauri star winds/envelopes could also apply to many of the Herbig stars. We favor the model discussed in our accompanying paper on the T Tauri stars; e.g., where the strong and broad emission lines form in dense turbulent regions that are generated at a star-accretion disk boundary layer and reside primarily near the disk plane. This conflicts with previous models of Herbig star envelopes that invoke the star as the driving force behind the winds and dense line-emitting gas. We also estimate the Ca II emissivity from dense envelopes near hot stars using photoionization calculations. We find that the Ca II lines of most Herbig stars could form very near the photosphere. Therefore, the T Tauri star models of dense turbulent envelopes near the star might apply directly. However, the early B stars require more extended high-density regions. Their sometimes double-peaked line profiles and general spectral similarity to the classical Be stars

  14. Searching for γ-ray emission from Reticulum II by Fermi-LAT

    Science.gov (United States)

    Zhao, Yi; Bi, Xiao-Jun; Yin, Peng-Fei; Zhang, Xinmin

    2018-02-01

    Recently, many new dwarf spheroidal satellites (dSphs) have been discovered by the Dark Energy Survey (DES). These dSphs are ideal candidates for probing for gamma-ray emissions from dark matter (DM) annihilation. However, no significant signature has been found by the Fermi-LAT dSph observations. In this work, we reanalyze the Fermi-LAT Pass 8 data from the direction of Reticulum II, where a slight excess has been reported by some previous studies. We treat Reticulum II (DES J0335.6-5403) as a spatially extended source, and find that no significant gamma-ray signature is observed. Based on this result, we set upper-limits on the DM annihilation cross section. Supported by National Natural Science Foundation of China (11121092, 11033005, 11375202, 11475191, 11475189), the CAS pilot B program (XDB23020000) and the National Key Program for Research and Development (2016YFA0400200)

  15. Emission Channeling Investigation of Implantation Defects and Impurities in II-VI-Semiconductors

    CERN Multimedia

    Trojahn, I; Malamud, G; Straver, J; Ronnqvist, C; Jahn, S-G; Restle, M

    2002-01-01

    Detailed knowledge on the behaviour of implantation damage and its influence on the lattice position and environment of implanted dopants in II-VI-compound semiconductors is necessary for a clear interpretation of results from other investigation methods and finally for technical utilization. Besides, a precise localization of impurities could help to clarify the discussion about the instability of the electrical properties of some dopants, called " aging ".\\\\ \\\\We intend to use the emission channeling method to investigate: \\\\ \\\\i) The behaviour of implantation damage which shall be probed by the lattice location of isoelectronic isotopes (Zn,Cd,Hg,Se,Te) directly after implantation at different temperatures, doses and vacancy densities and after annealing treatments, and ii) the precise lattice sites of the acceptor Ag and donor In under different conditions by implanting precursors Cd and In isotopes. \\\\ \\\\Further on we would like to test the application of a two-dimensional position and energy sensitive e...

  16. A new Ni(II complex as a novel and efficient recyclable catalyst for the synthesis of pyrano[2,3-d]pyrimidines

    Directory of Open Access Journals (Sweden)

    M. Habibi Kheirabadi

    2016-12-01

    Full Text Available A simple and highly efficient one-pot three-component synthesis of a series of pyrido[2,3-d]pyrimidines from the condensation of barbituric acid, malononitrile and aromatic aldehydes using catalytic amount of a new Ni(II complex based on 5-nitro-N1-((pyridin-2-ylmethylene benzene-1,2-diamine (NiL is reported. This new heterogeneous catalyst has the advantages of being environmentally friendly, simple work-up and high yields character.

  17. Fabry-perot for airborne infrared astronomy and the [Si II] emission from the galactic center

    International Nuclear Information System (INIS)

    Graf, P.H.

    1988-01-01

    A Fabry-Perot spectrometer for infrared astronomy was built for and used on NASA's Kuiper Airborne Observatory. This instrument produces very high resolution spectra between 15 and 50 μm. The Fabry-Perot uses free-standing metal mesh for its optical resonant cavity and servo-controlled motors to vary the transmitted wavelengths. The fine-structure lines of [S III] to 18.71 μm (M42) and 33.482 μm (M17) in Galactic HII regions and [Si II] at 34.816 μm (S 106) in a photodissociation region (PDR) were observed with the Fabry-Perot. The distribution of the [Si II] 34.816-μm emission from within 5 parsecs of the Galactic center is measured with the Cornell high-resolution grating spectrometer, which is also used as the order-sorter for the Fabry-Perot. The gas-phase abundance of silicon within the neutral gas ring surrounding the Galactic center is 4.5 x 10 -6 . The Si II 34.8-μm/O I 63.2-μm line ratio is independent of the emitting region temperature and density, so the relative abundance of Si II to O I may be determined directly

  18. Efficiency of Aluminum and Iron Electrodes for the Removal of Heavy Metals [(Ni (II), Pb (II), Cd (II)] by Electrocoagulation Method

    Energy Technology Data Exchange (ETDEWEB)

    Khosa, Muhammad Kaleem; Jamal, Muhammad Asghar; Hussain, Amira; Muneer, Majid; Zia, Khalid Mahmood [Government College Univ., Faisalabad (Pakistan); Hafeez, Samia [Bahaud-din-Zakariya Univ., Multan (Pakistan)

    2013-06-15

    Electrocoagulation (EC) technique is applied for the treatment of wastewater containing heavy metals ions such as nickel (Ni), lead (Pb) and cadmium (Cd) by using sacrificial anodes corrode to release active coagulant flocs usually aluminium or iron cations into the solution. During electrolytic reactions hydrogen gas evolve at the cathode. All the experiments were carried out in Batch mode. The tank was filled with synthetic wastewater containing heavy metals and efficiency of electrocoagulation in combination with aluminum and iron electrodes were investigated for removal of such metals. Several parameters, such as contact time, pH, electro-coagulant concentration, and current density were optimized to achieve maximum removal efficiency (%). The concentrations of heavy metals were determined by using Atomic Absorption Spectroscopy (AAS). It is found that the electro-coagulation process has potential to be utilized for the cost-effective removal of heavy metals from wastewater specially using iron electrodes in terms of high removal efficiencies and operating cost.

  19. Simultaneous removal of Cd(II), Ni(II), Pb(II) and Cu(II) ions via their complexation with HBANSA based on a combined ultrasound-assisted and cloud point adsorption method using CSG-BiPO4/FePO4as novel adsorbent: FAAS detection and optimization process.

    Science.gov (United States)

    Kheirandish, Shadi; Ghaedi, Mehrorang; Dashtian, Kheibar; Jannesar, Ramin; Montazerozohori, Morteza; Pourebrahim, Faezeh; Zare, Mohammad Ali

    2017-08-15

    Ultrasound irradiation, cloud point and adsorption methods were coupled to develop a new technique for the simultaneous removal of Cd(II), Ni(II), Pb(II) and Cu(II) ions after their complexation with (E)-4-((2-hydroxybenzylidene) amino) naphthalene-1-sulfonic acid (HBANSA). In order to reduce cost and improve practicability of process, chitosan gel (CSG) composited with bismuth(III) phosphate/iron(III) phosphate nanoparticles (CSG-BiPO 4 /FePO 4 ) were hydrothermally synthesized followed by their characterization using FE-SEM, EDS and XRD analysis. The operational parameters such as metal ions concentration, CSG-BiPO 4 /FePO 4 mass, sonication time and temperature were investigated and optimized using central composite design (CCD). In addition, the possible significant correlation between these variables and removal efficiency was studied from which the maximum efficiencies were obtained at 5.57mg/L, 51.49°C, 0.018g and 10.73min corresponding to metal ions concentration, temperature, CSG-BiPO 4 /FePO 4 and sonication time, respectively. Moreover, at these conditions, the removal percentages of the Cd(II), Ni(II), Pb(II) and Cu(II) ions were found to be 96.24, 93.73, 95.55 and 97.47, respectively. After applying various isotherms, the Langmuir isotherm model was found to be most appropriate model for describing and fitting the experimental equilibrium data and thus maximum mono-layer adsorption capacities of 8.61, 8.54, 8.65 and 8.62mgg -1 were obtained for Cd(II), Pb(II), Cu(II) and Ni(II) ions, respectively. The study of kinetics showed well applicability of pseudo second order kinetic model with maximum mass transfer rate in adsorption process. Copyright © 2017 Elsevier Inc. All rights reserved.

  20. Application of Sayong Ball Clay Membrane Filtration for Ni (II Removal from Industrial Wastewater

    Directory of Open Access Journals (Sweden)

    S.F. Mohd Noor

    2017-11-01

    Full Text Available Wastewater containing heavy metals, such as nickel ions (Ni2+, discharged from industry to water streams poses a serious threat because even at low concentrations, it does not naturally degrade and is toxic to human and aquatic life. This article reviews a novel technique for wastewater treatment using a Sayong ball clay (SBC membrane to remove nickel from industrial wastewater. SBC powder was achieved through milling using a planetary ball mill (milling time; 10, 20 and 30 h, further labelled as SBC 10, SBC 20 and SBC 30, with a ball-to-powder of ratio 7:1 and rotation speed of 300 rpm. The physical characteristics of the apparent porosities, bulk density and shrinkage were investigated. XRD was used to study the phase, while FESEM was used to analyse the microstructure of the fired membrane. The FESEM microstructure indicates a decreased particle size (SB30. Filtration was conducted using a dead-end filtration system. The fabricated SBC 10, 20 and 30 membranes showed significant removal of nickel from industrial wastewater—88.87%, 82.96% and 85.13%, respectively. This study revealed that the SBC membrane is a promising membrane to remove nickel from industrial wastewater. The results also indicate the possibility of highlighting the introduced technique as a new technique for the treatment of industrial wastewater. As a new trend for waste management, pollution prevention could be applied in Malaysia as one of the advanced biotechnologies to solve various environmental problems. Keywords: environmental management, wastewater treatment, waste processing, heavy metals

  1. Synthesis and characterization of novel M(II (M = Mn(II, Ni(II, Cu(II or Zn(II complexes with tridentate N2,O-donor ligand (E-2-amino-N’-[1-(pyridin-2-yl- ethylidene]benzohydrazide

    Directory of Open Access Journals (Sweden)

    C. H. Kane

    2016-02-01

    Full Text Available The coordination chemistry towards the M(II metal centre (M = Mn, Ni, Cu or Zn of the hydrazone ligand (E-2-amino-N’-[1-(pyridin-2-ylethylidene]benzohydrazide (H3L has been explored and complexes having formulae [Mn(H2L2] (1, {[Ni(H2L2].DMF.0.4H2O} (2, {[Cu2(H2L2(µ-Cl2].DMF} (3 and [Zn(H2L2] (4 have been isolated and characterized by IR, UV-Visible spectroscopy, elemental analysis and X-ray crystal diffraction. Structural studies reveal that the mononuclear complexes (1, (2 and (4 adopt highly distorted octahedral geometries while the dinuclear complex (3 adopts a square pyramidal geometry around each copper(II ion. DOI: http://dx.doi.org/10.4314/bcse.v30i1.9

  2. Substitutional impact on biological activity of new water soluble Ni(II) complexes: Preparation, spectral characterization, X-ray crystallography, DNA/protein binding, antibacterial activity and in vitro cytotoxicity.

    Science.gov (United States)

    Umadevi, C; Kalaivani, P; Puschmann, H; Murugan, S; Mohan, P S; Prabhakaran, R

    2017-02-01

    A series of new water soluble nickel(II) complexes containing triphenylphosphine and 4-methoxysalicylaldehyde-4(N)-substituted thiosemicarbazones were synthesized and characterized. Crystallographic investigations confirmed the structure of the complexes (1-4) having the general structure [Ni(4-Msal-Rtsc)(PPh 3 )] (Where R=H (1); CH 3 (2); C 2 H 5 (3); C 6 H 5 (4)) which showed that thiosemicarbazone ligands coordinated to nickel(II) ion as ONS tridentate bibasic donor. DNA/BSA protein binding ability of the ligands and their new complexes were studied by taking calf-thymus DNA (CT-DNA) and Bovine serum albumin (BSA) through absorption and emission titrations. Ethidium bromide (EB) displacement study showed the intercalative binding trend of the complexes to DNA. From the albumin binding studies, the mechanism of quenching was found as static and the alterations in the secondary structure of BSA by the compounds were confirmed with synchronous spectral studies. The binding affinity of the complexes to CT-DNA and BSA has the order of [Ni(4-Msal-etsc)(PPh 3 )] (3) >[Ni(4-Msal-mtsc)(PPh 3 )] (2) >[Ni(4-Msal-tsc)(PPh 3 )] (1) >[Ni(4-Msal-ptsc)(PPh 3 )] (4). In vitro cytotoxicity of the complexes was tested on human lung cancer cells (A549), human cervical cancer cells (HeLa), human liver carcinoma cells (Hep G2). All the complexes exhibited significant activity against three cancer cells. Among them, complex 4 exhibited almost 2.5 fold activity than cisplatin in A549 and HepG2 cell lines. In HeLa cell line, the complexes exhibited significant activity which is less than cisplatin. While comparing the activity of the complexes in A549 and HepG2 cell lines it falls in the order 4>1>2>3>cisplatin. The results obtained from DNA, protein binding and cytotoxicity studies, it is concluded that the cytotoxicity of the complexes as determined by MTT assay were not unduly influenced by the complexes having different binding efficiency with DNA and protein. The complexes

  3. Effect of the organic matter on the adsorption of Eu(III)/Ni(II) onto the Callovo-Oxfordian clay-stone from Bure (France)

    Energy Technology Data Exchange (ETDEWEB)

    Azouazi, M.; Montavon, G.; Grambow, B. [UMR 6457 SUBATECH, Ecole des Mines de Nantes, BP 20722, 44307, Nantes cedex 3 (France); Michels, R. [UMR CNRS 7566 G2R, BP 236, 54501 Vandoeuvre les Nancy Cedex (France); Reiller, P. [CEA, DEN/DPC, 91191 Gif sur Yvette Cedex (France); Mercier, F.; Moulin, V. [UMR CEACNRS- UEVE 8587, 91191 Gif sur Yvette Cedex (France)

    2005-07-01

    Full text of publication follows: This work aimed to study the contribution of organic matter on the retention of Eu(III) and Ni(II) on the Callovo-Oxfordian clay-stone from the underground laboratory site of Bure (France). The investigation was based on the study of the raw clay-stone as well as experimentally oxidized samples to test the effects of air alteration on the retention potential of Eu(III) and Ni(II). X-ray diffraction and XPS photoelectron spectroscopy reveal that the chemistry of the minerals is not significantly affected by oxidation, nor is the specific surface of the samples. On the contrary, the organic material shows clear alteration. The oxidation of the kerogen leads to an increase of the extractable hydrocarbons amounts from 6 to 15{mu}g/g of rock after 1024 h of oxidation. The kerogen as well as the extractable polar compounds are enriched in oxygenated compounds (especially carboxylic acid functions as revealed by pyrolysis-gcms and FTIR). In the presence of clay water, the organic matter is not significantly mobilized, and this irrespective of its oxidation degree. Furthermore, the effect of the colloidal phase on the retention could be neglected. Oxidation increases significantly the retention capacity of the clay-stone. The removal of the dichloromethane soluble fraction did not lead to a significant decrease in Kd values for Eu(III) and Ni(II). A slight increase was rather observed for Ni(II), indicating that new adsorption sites may have been made accessible. The chloroform extractable fraction may therefore not be an important fraction for the adsorption process. It was shown that minerals, with the exception of pyrite, are not significantly affected by air oxidation, while kerogen is. The increase of adsorption after oxidation may be attributed to the formation of new oxygenated organic functions in the kerogen. Quantitative analysis of the data using a multi-site Langmuir model (one site is the clay+calcite while the second is the

  4. Inter-comparison between Hermesv2.0 and TNO-MAC-II emission data using the Caliope air quality system (Spain)

    NARCIS (Netherlands)

    Guevara, M.; Pay, M.T.; Martinez, F.; Soret, A.; Denier van der Gon, H.A.C.; Baldasano, J.M.

    2014-01-01

    This work examines and compares the performance of two emission datasets on modelling air quality concentrations for Spain: (i) the High-Elective Resolution Modelling Emissions System (HERMESv2.0) and (ii) the TNO-MACC-II emission inventory. For this purpose, the air quality system CALIOPE-AQFS

  5. Mg II Chromospheric Emission Line Bisectors Of HD39801 And Its Relation With The Activity Cycle

    Science.gov (United States)

    García García, Leonardo Enrique; Pérez Martínez, M. Isabel

    2016-07-01

    Betelgeuse is a cool star of spectral type M and luminosity class I. In the present work, the activity cycle of Betelgeuse was obtained from the integrated emission flux of the Mg II H and K lines, using more than 250 spectra taken from the International Ultraviolet Explorer (IUE) online database. Of which it was found, based on a Lomb Scargle periodogram, a cycle of 16 years, along with 2 sub-cycles with a period of the order of 0.60 and 0.65 years, which may be due to turbulence or possible stellar flares. In addition, an analysis of line asymmetry was made by means of the chromospheric emission line bisectors, due to the strong self-absorption observed in this lines, the blue and red wings were analyzed independently. In order to measure such asymmetry, a "line shift" was calculated, from which several cycles of variability were obtained from a Lomb Scargle periodogram, spanning from few months to 4 years. In the sense, the most significant cycle is about 0.44 and 0.33 years in the blue and red wing respectively. It is worth noting, that the rotation period of the star doesn't play an important role in the variability of the Mg II lines. This technique provides us with a new way to study activity cycles of evolved stars.

  6. Search for [C II] emission in z = 6.5-11 star-forming galaxies

    International Nuclear Information System (INIS)

    González-López, Jorge; Infante, Leopoldo; Riechers, Dominik A.

    2014-01-01

    We present the search for the [C II] emission line in three z > 6.5 Lyα emitters (LAEs) and one J-dropout galaxy using the Combined Array for Research in Millimeter-wave Astronomy and the Plateau de Bure Interferometer. We observed three bright z ∼ 6.5-7 LAEs discovered in the Subaru Deep Field (SDF) and the multiple imaged lensed z ∼ 11 galaxy candidate found behind the galaxy cluster MACSJ0647.7+7015. For the LAEs IOK-1 (z = 6.965), SDF J132415.7+273058 (z = 6.541), and SDF J132408.3+271543 (z = 6.554) we find upper limits for the [C II] line luminosity of <2.05, <4.52, and <10.56 × 10 8 L ☉ , respectively. We find upper limits to the far-IR (FIR) luminosity of the galaxies using a spectral energy distribution template of the local galaxy NGC 6946 and taking into account the effects of the cosmic microwave background on the millimeter observations. For IOK-1, SDF J132415.7+273058, and SDF J132408.3+271543 we find upper limits for the FIR luminosity of <2.33, 3.79, and 7.72 × 10 11 L ☉ , respectively. For the lensed galaxy MACS0647-JD, one of the highest-redshift galaxy candidates to date with z ph =10.7 −0.4 +0.6 , we put an upper limit in the [C II] emission of <1.36 × 10 8 × (μ/15) –1 L ☉ and an upper limit in the FIR luminosity of <6.1 × 10 10 × (μ/15) –1 L ☉ (where μ is the magnification factor). We explore the different conditions relevant for the search for [C II] emission in high-redshift galaxies as well as the difficulties for future observations with the Atacama Large Millimeter/submillimeter Array (ALMA) and the Cerro Chajnantor Atacama Telescope (CCAT).

  7. Synthesis, Crystal Structures, Magnetic Properties, and Theoretical Investigation of a New Series of NiII-LnIII-WVHeterotrimetallics: Understanding the SMM Behavior of Mixed Polynuclear Complexes.

    Science.gov (United States)

    Vieru, Veacheslav; Pasatoiu, Traian D; Ungur, Liviu; Suturina, Elizaveta; Madalan, Augustin M; Duhayon, Carine; Sutter, Jean-Pascal; Andruh, Marius; Chibotaru, Liviu F

    2016-12-05

    The polynuclear compounds containing anisotropic metal ions often exhibit efficient barriers for blocking of magnetization at fairly arbitrary geometries. However, at variance with mononuclear complexes, which usually become single-molecule magnets (SMM) under the sole requirement of a highly axial crystal field at the metal ion, the factors influencing the SMM behavior in polynuclear complexes, especially, with weakly axial magnetic ions, still remain largely unrevealed. As an attempt to clarify these conditions, we present here the synthesis, crystal structures, magnetic behavior, and ab initio calculations for a new series of Ni II -Ln III -W V trimetallics, [(CN) 7 W(CN)Ni(H 2 O)(valpn)Ln(H 2 O) 4 ]·H 2 O (Ln = Y 1, Eu 2, Gd 3, Tb 4, Dy 5, Lu 6). The surprising finding is the absence of the magnetic blockage even for compounds involving strongly anisotropic Dy III and Tb III metal ions. This is well explained by ab initio calculations showing relatively large transversal components of the g-tensor in the ground exchange Kramers doublets of 1 and 4 and large intrinsic tunneling gaps in the ground exchange doublets of 3 and 5. In order to get more insight into this behavior, another series of earlier reported compounds with the same trinuclear [W V Ni II Ln III ] core structure, [(CN) 7 W(CN)Ni(dmf)(valdmpn)Ln(dmf) 4 ]·H 2 O (Ln = Gd III 7, Tb III 8a, Dy III 9, Ho III 10), [(CN) 7 W(CN)Ni(H 2 O)(valdmpn)Tb(dmf) 2.5 (H 2 O) 1.5 ]·H 2 O·0.5dmf 8b, and [(CN) 7 W(CN)Ni(H 2 O)(valdmpn)Er(dmf) 3 (H 2 O) 1 ]·H 2 O·0.5dmf 11, has been also investigated theoretically. In this series, only 8b exhibits SMM behavior which is confirmed by the present ab initio calculations. An important feature for the entire series is the strong ferromagnetic coupling between Ni(II) and W(V), which is due to an almost perfect trigonal dodecahedron geometry of the octacyano wolframate fragment. The reason why only 8b is an SMM is explained by positive zero-field splitting on the nickel

  8. Self-assembly of mixed-valence Co(II/III) and Ni(II) clusters: azide-bridged 1D single chain coordination polymers comprised of tetranuclear units, tetranuclear Co(II/III) complexes, ferromagnetically coupled azide-bridged tetranuclear, and hexanuclear Ni(II) complexes: synthesis, structural, and magnetic properties.

    Science.gov (United States)

    Tandon, Santokh S; Bunge, Scott D; Rakosi, Robert; Xu, Zhiqiang; Thompson, Laurence K

    2009-09-07

    One-pot reactions between 2,6-diformyl-4-methylphenol (DFMP) and 2-aminoethanol (AE) in the presence of cobalt(II) salts [Co(ClO4)2, CoCl2, Co(CH3CO2)2, Co(NO3)2] and sodium azide result in the self-assembly of novel one-dimensional single chain mixed-valence cobalt coordination polymers {[Co2(II)Co2(III) (HL)2(OCH3)2(N3)3]ClO(4).5H2O.CH3OH}n (1), {[Co2(II)Co2(III) (HL)2(OCH3)2(N3)3]Cl.H2O}n (2) in which tetra-cobalt cationic units are bridged by symmetrical 1,3-azides, forming single chains; mixed valence neutral tetranuclear clusters [Co2(II)Co2(III) (HL)2(OCH3)2(N3)4]CH3OH.2H2O (3), [Co2(II)Co2(III)(HL)2(OCH3)2(N3)2(CH3CO2)2].2CH3OH.2H2O (4), and the cationic cluster [Co2(II) Co2(III) (HL)2(OCH3)2(CH3OH)2(N3)2](NO3)2 (5). In all these reactions, H3L, the potentially pentadentate (N2O3), trianionic double Schiff base ligand 2,6-bis[(2-hydroxy-ethylimino)-methyl]-4-methylphenol is formed. The reaction between DFMP and AE in the presence of nickel(ii) salts and sodium azide in methanol-water mixture results in the self-assembly of ferromagnetically coupled hexanuclear complexes [Ni6(H2L)2(HL-1)2(H2O)2(N3)6](ClO4)(2).2CH3OH (6), and [Ni6(H2L)2(HL-1)2(CH3OH)2(N3)6](BF4)2 (7), involving double (H3L) and single (H2L-1) Schiff base ligands, and a neutral tetranuclear complex [Ni4(H2L)2(OCH3)2(CH3CO2)2(N3)2] (8) with only double Schiff-base (H3L). In these complexes, the nature of the anion and the reaction conditions seem to play an important role in directing the formation of tetranuclear, hexanuclear or polymeric clusters. All complexes involve divacant double cubane-type cores containing three to four different types of bridging ligands (phenoxy, azido, methoxy/alkoxy, and acetate). Variable temperature magnetic properties of these spin coupled clusters have been investigated and magneto-structural correlations have been established.

  9. Design and testing of an electron Bernstein wave emission radiometer for the TJ-II Stellarator

    International Nuclear Information System (INIS)

    Caughman, J.B.O.; Rasmussen, D.A.; Carter, M.C.; Wilgen, J.B.; Cappa, A.; Castejon, F.; Fernandez, A.

    2005-01-01

    Efficient Electron Bernstein wave (EBW) mode conversion is important for heating dense plasmas in TJ-II. The O-X-B mode conversion scenario is being considered for heating plasmas with densities over 1,3 x 10 19 m -3 , which will be very interesting to study high-density physics and for heating NBI plasmas. Measurement of the thermal EBW emission from the plasma allows the EBW mode conversion efficiency to be determined, and also has the potential to offer a diagnostic for measuring electron temperature profile evolution in overdense plasmas. A dual-polarized quad-ridged broadband horn with a focusing lens will be used to measure the EBW emission at 28 GHz on TJ-II. A focused beam is needed to achieve efficient coupling at the mode conversion layer. Emission from the plasma is reflected from a steerable internal mirror, propagates through a glass lens, and is focused on the horn. The field pattern from the horn-lens combination has been measured as a function of horn-lens spacing and lens focal length with a 3-D scanning system in an effort to minimize the beam waist at the plasma edge. Beam waist sizes have been measured at distances of up to 80 cm from the lens. Details of the experimental results and future plans will be presented. [Oak Ridge National Laboratory is managed by UT-Battelle, LLC, for the U.S. Dept. of Energy under contract DE-AC05-00OR22725. A part of this work is performed under support of Spanish 'Subdireccion General de Proyectos de Investigacion, Ministerio de Educacion y Ciencia' with reference ENE2004-06957]. (author)

  10. Separation Studies of Pd(II from Acidic Chloride Solutions of Pt(IV, Ni(II and Rh(III by Using 4-Aroyl-3-Phenyl-5-Isoxazolones

    Directory of Open Access Journals (Sweden)

    Koduru Janardhan Reddy

    2012-01-01

    Full Text Available This study examined the effect influence of various factors on the extraction of Pd(II to develop a new liquid-liquid extraction mechanism for the selective separation of palladium(II from its acidic chloride solutions using 4-aroyl-3-phenyl-5-isoxazolones (HA, such as 3-phenyl-4-(4-fluorobenzoyl-5- isoxazolone (HFBPI, 3-phenyl-4-benzoyl-5-isoxazolone (HPBI and 3-phenyl-4- (4-toluoyl-5-isoxazolone (HTPI. The extraction strength of Pd(II with HA were in the following order: HFBPI > HPBI > HTPI, which is opposite to that observed with their pKa values. HPBI was used to separate Pd(II from Pt(IV, Ni(II and Rh(III metal ions and calculated their separation factors (S.F. were followed in the order: Pd/Ni (40±0.4 > Pd/Pt (25±0.2 > Pd/Rh (15±0.3 > Rh/Ni (2.7±0.3 > Pt/Ni ≈ Rh/Pt (1.7±0.2. The loading and striping of Pd(II (1.12×10-4 mol L-1 were also examined using 1.0×10-3 mol L-1 HPBI in CHCl3 and 1.0 mol L-1 HCl, respectively. The results demonstrated that the maximum (97.5% extraction and desorption (89% of metal required at least 3.0 cycles. The developed method was applied successfully to the separation of palladium from synthetic water samples.

  11. First light - II. Emission line extinction, population III stars, and X-ray binaries

    Science.gov (United States)

    Barrow, Kirk S. S.; Wise, John H.; Aykutalp, Aycin; O'Shea, Brian W.; Norman, Michael L.; Xu, Hao

    2018-02-01

    We produce synthetic spectra and observations for metal-free stellar populations and high-mass X-ray binaries in the Renaissance Simulations at a redshift of 15. We extend our methodology from the first paper in the series by modelling the production and extinction of emission lines throughout a dusty and metal-enriched interstellar and circum-galactic media extracted from the simulation, using a Monte Carlo calculation. To capture the impact of high-energy photons, we include all frequencies from hard X-ray to far-infrared with enough frequency resolution to discern line emission and absorption profiles. The most common lines in our sample in order of their rate of occurrence are Ly α, the C IV λλ1548, 1551 doublet, H α, and the Ca II λλλ8498, 8542, 8662 triplet. The best scenario for a direct observation of a metal-free stellar population is a merger between two Population III Galaxies. In mergers between metal-enriched and metal-free stellar populations, some characteristics may be inferred indirectly. Single Population III galaxies are too dim to be observed photometrically at z = 15. Ly α emission is discernible by JWST as an increase in J200w - J277w colour off the intrinsic stellar tracks. Observations of metal-free stars will be difficult, though not impossible, with the next generation of space telescopes.

  12. On the Lack of Correlation Between Mg II 2796, 2803 Angstrom and Lyman alpha Emission in Lensed Star-Forming Galaxies

    Science.gov (United States)

    Rigby, Jane Rebecca; Bayliss, M. B.; Gladders, M. D.; Sharon, K.; Wuyts, E.; Dahle, H.

    2014-01-01

    We examine the Mg II 2796, 2803 Angstrom, Lyman alpha, and nebular line emission in five bright star-forming galaxies at 1.66 less than z less than 1.91 that have been gravitationally lensed by foreground galaxy clusters. All five galaxies show prominent Mg II emission and absorption in a P Cygni profile. We find no correlation between the equivalent widths of Mg II and Lyman alpha emission. The Mg II emission has a broader range of velocities than do the nebular emission line profiles; the Mg II emission is redshifted with respect to systemic by 100 to 200 km s(exp-1). When present, Lyman alpha is even more redshifted. The reddest components of Mg II and Lyman alpha emission have tails to 500-600 km s(exp-1), implying a strong outflow. The lack of correlation in the Mg II and Lyman alpha equivalent widths, the differing velocity profiles, and the high ratios of Mg II to nebular line fluxes together suggest that the bulk of Mg II emission does not ultimately arise as nebular line emission, but may instead be reprocessed stellar continuum emission.

  13. Synthesis, spectroscopic and single crystal X-ray studies on three new mononuclear Ni(II) pincer type complexes: DFT calculations and their antimicrobial activities

    Science.gov (United States)

    Layek, Samaresh; Agrahari, Bhumika; Tarafdar, Abhrajyoti; Kumari, Chanda; Anuradha; Ganguly, Rakesh; Pathak, Devendra D.

    2017-08-01

    Three new mononuclear square planar Ni(II) complexes, containing pincer type tridentate Schiff base ligands, having general formula [(NiL1(4-MePy)] (1), [(NiL1(2-AzNp)] (2), and [(NiL2(4-MePy)] (3) [where L1 = anion of N-(2-hydroxy-3-methoxybenzylidene) benzoylhydrazide (HL1), L2 = anion of N-(2-hydroxy-3-methoxybenzylidene) thiosemicarbazide (HL2), 4-MePy = 4-Methylpyridine and 2-AzNp = 2-Azanapthalene] have been synthesized and fully characterized by FT-IR, UV-visible, NMR, single crystal X-ray diffraction studies and elemental analysis. All the three complexes show square planar geometry around the nickel atom. The pincer type ligand occupies three coordination sites, while the fourth site is occupied by the monodentate nitrogen containing ligand. The Quantum chemical DFT calculations have also been carried out using DFT/B3LYP method and 6-311++G(d,p) basis set. The synthesized nickel complexes were screened for antimicrobial activities by agar well diffusion method against E. coli bacteria. Out of three complexes, [(NiL2(4-MePy)] (3) only showed the antimicrobial activity against E. coli bacteria.

  14. Assignment of solid-state 13C and 1H NMR spectra of paramagnetic Ni(II) acetylacetonate complexes aided by first-principles computations

    DEFF Research Database (Denmark)

    Rouf, Syed Awais; Jakobsen, Vibe Boel; Mareš, Jiří

    2017-01-01

    Recent advances in computational methodology allowed for first-principles calculations of the nuclear shielding tensor for a series of paramagnetic nickel(II) acetylacetonate complexes, [Ni(acac)2L2] with L = H2O, D2O, NH3, ND3, and PMe2Ph have provided detailed insight into the origin of the par......Recent advances in computational methodology allowed for first-principles calculations of the nuclear shielding tensor for a series of paramagnetic nickel(II) acetylacetonate complexes, [Ni(acac)2L2] with L = H2O, D2O, NH3, ND3, and PMe2Ph have provided detailed insight into the origin...

  15. Preparation and Characterization of Poly(ethyl hydrazide Grafted Oil Palm Empty Fruit Bunch for Removal of Ni(II Ion in Aqueous Environment

    Directory of Open Access Journals (Sweden)

    Siti Mariam Mohd Nor

    2013-07-01

    Full Text Available Poly(ethyl hydrazide grafted oil palm empty fruit bunch (peh-g-opefb fiber has been successfully prepared by heating poly(methylacrylate-g-opefb at 60 °C for 4 h in a solution of hydrazine hydrate in ethanol. The chelating ability of peh-g-opefb was evaluated based on removal of Ni(II ions in aqueous solution. Adsorption of Ni(II by peh-g-opefb was characterized based on effect of pH, isotherm, kinetic and thermodynamic study. This cheap sorbent based on oil palm empty fruit bunch fiber has a great future potential in water treatment industries based on high adsorption capacity, biodegradability and renewability.

  16. Developing of risk-hedging CO2-emission policy. Part II: risks associated with measures to limit emissions, synthesis and conclusions

    International Nuclear Information System (INIS)

    Harvey, L.D.D.

    1996-01-01

    This paper is Part II of a two-part series in which the risk associated with unrestrained greenhouse-gas emissions, and with measures to limit emissions, are reviewed. The following risks associated with these efforts to limit CO 2 emissions are reviewed here: (1) resources might be diverted from other urgent needs; (2) economic growth might be reduced; (3) reduction measures might cost more than expected; (4) early action might cost more than later action; (5) reduction measures might have undesired side effects; (6) reduction measures might require heavy-handed government intervention; and (7) reduction measures might not work. With gradual implementation of a diversified portfolio of measures, these risks can be greatly reduced. Based on the review of risks associated with measures to limit emissions here, and the review of the risk associated with unrestrained emissions presented in Part I, it is concluded that a reasonable near-term (20-30 year) risk hedging strategy is one which seeks to stabilize global fossil CO 2 emissions at the present (early 1990s) level. This is turn implies an emission reduction of 26% for industrialized countries as a whole and 40-50% for Canada and the USA if developing country emissions are to increase by no more than 60%, which in itself would require major assistance from the industrialized countries. The framework and conclusions presented here are critically compared with so-called optimization frameworks. 82 refs., 2 figs., 2 tabs

  17. New dual emission fluorescent sensor for pH and Pb(II) based on bis(napfthalimide) derivative

    Energy Technology Data Exchange (ETDEWEB)

    Pina-Luis, Georgina, E-mail: gpinaluis@yahoo.com [Centro de Graduados e Investigacion en Quimica, Instituto Tecnologico de Tijuana, AP 1166, Tijuana 22500, BC (Mexico); Martinez-Quiroz, Marisela; Ochoa-Teran, Adrian [Centro de Graduados e Investigacion en Quimica, Instituto Tecnologico de Tijuana, AP 1166, Tijuana 22500, BC (Mexico); Santacruz-Ortega, Hisila [Departamento de investigacion en Polimeros y Materiales, Universidad de Sonora, Hermosillo, Sonora 83000 (Mexico); Mendez-Valenzuela, Eduardo [Centro de Graduados e Investigacion en Quimica, Instituto Tecnologico de Tijuana, AP 1166, Tijuana 22500, BC (Mexico)

    2013-02-15

    This paper describes a novel dual emission bis-1,8-naphthalimide sensor for selective determination of pH and Pb{sup 2+} ions. The influence of the variability in the backbone that links the two fluorophores (naphthalimides) as a function of pH and metal ions was studied by UV-visible and fluorescence spectroscopy. Compounds 1(a-d) with different length alkyl linkers (CH{sub 2}){sub n} (n=1, 2, 4 and 6) showed no excimer formation in aqueous solution. Fluorescence emission of these derivatives varied in a narrow range of pH (5-8) and was only slightly influenced by the addition of metal ions in CH{sub 3}CN solutions. However, derivative 1e with amino-containing spacer (CH{sub 2}-NH-CH{sub 2}) showed excimer emission in aqueous solution, a wide response to pH (2.5-9.5) and fluorescence enhancement with selective behavior towards metal ions. The pH sensor based in derivative 1e has a sufficient selectivity for practical pH monitoring in the presence of Li{sup +}, Na{sup +}, K{sup +}, Cs{sup +}, Ca{sup 2+}, Mg{sup 2+}, Ba{sup 2+}, Cu{sup 2+}, Pb{sup 2+}, Ni{sup 2+}, Zn{sup 2+} and Cd{sup 2+}. The coordination chemistry of these complexes was studied by UV-Vis, fluorescence and {sup 1}H NMR. This chemosensor displayed high selectivity fluorescence enhancement toward Pb{sup 2+} ions in the presence of the metals ions mentioned in CH{sub 3}CN solutions. Competitive assays show that a 1-fold of metal cations in each case, compared with Pb{sup 2+} ions, results in less than {+-}5% fluorescence intensity changes. Linear calibration up to 1 Multiplication-Sign 10{sup -5} M for Pb(II) ions (R=0.9968) was obtained and detection limit resulted of 5.0 Multiplication-Sign 10{sup -8} M. - Highlights: Black-Right-Pointing-Pointer A novel dual emission bis-1,8-naphthalimide sensor for pH and Pb{sup 2+} ions is synthetized. Black-Right-Pointing-Pointer The excimer formation depends on the spacer that links the two naphthalimide groups. Black-Right-Pointing-Pointer Bis

  18. A Paper-Based Analytical Device Based on Combination of Thin Film Microextraction and Reflection Scanometry for Sensitive Colorimetric Determination of Ni(II) in Aqueous Matrix.

    Science.gov (United States)

    Allafchian, Ali Reza; Farajmand, Bahman; Koupaei, Amin Javaheri

    2018-02-19

    In this research, the thin film microextraction method was applied for the extraction of Ni(II) ion from aqueous matrixes. Chemically modified cellulosic filter paper with phosphorus was used as a thin film extractor. After extraction, the thin film was treated with a solution of dimethylglyoxime. The colored film was captured by flatbed scanner and the absorbance of the images was extracted by some suitable software. Under the optimum conditions and at the pH 7.0, with the sample volume of 100 mL, the stirring rate of 800 rpm, and the extraction time of 50 min, the calibration curve was obtained in the range of 0.05-5 mg/L Ni(II) (R 2  = 0.989). Limit and relative standard deviation were achieved to be 18 µg/L and less than 6.7%, respectively. Relative recoveries were obtained in the range of 87%-105%. Finally, the proposed method was found to be simple and cost-effective, with adequate analytical performance for the rapid detection of Ni(II) in river and wastewater samples.

  19. Atomic data of Ti II from laser produced Ti plasmas by optical emission spectroscopy

    International Nuclear Information System (INIS)

    Refaie, A.I.; Farrag, A.A.; El Sharkawy, H.; El Sherbini, T.M.

    2005-06-01

    In the present study, the emission spectrum of titanium produced from laser induced plasma has been measured at different distances from the target. The Titanium target is irradiated by using the high power Q-switched Nd:YAG laser (λ=1064 nm) that generates energy 750 mJ/pulse of duration rate 6 ns and repetition rate 10 Hz in vacuum and at different distances. The variation of the distance from the target affects the measured plasma parameters, i.e. the electron density, the ion temperature and the velocity distribution. The electron density increases with the increase of the distance from the target. At a distance 0.6 mm from the target it decreases to 2.28·10 16 cm -3 . The temperature increases with the distance from the get until a distance of 1 mm, after that it decreases. It is found that the plasma velocity increases with the distance then it decreases again. Then, Energy levels and transition probabilities for 3d 2 4p →(3d 2 4s + 3d 3 ) lines have been determined by measurement of emission line intensities from an optically thin laser produced plasma of Ti II in vacuum. Calculations with intermediate coupling using Hartree-Fock wave functions have been carried out in order to place the experimental data on an absolute scale and also to evaluate the lifetimes. The plasma parameters in different regions of the plasma plume have been measured and used to obtain further transition probabilities. (author)

  20. Clinical Imaging Characteristics of the Positron Emission Mammography PEM Flex Solo II.

    Science.gov (United States)

    Macdonald, Lawrence; Edwards, John; Lewellen, Thomas; Rogers, James; Kinahan, Paul

    2008-10-01

    Positron emission mammography (PEM) uses two opposing gamma-ray imagers and limited-angle tomography techniques to image radiotracer distributions within the breast. Due to their smaller size and closer proximity to the source, dedicated PEM cameras can provide better spatial resolution and count sensitivity than whole-body positron emission tomographs. We performed several clinical imaging tests on a commercially available PEM camera, the PEM Flex Solo II. This system is comprised of two opposing 6 cm × 16.4 cm detectors that scan in unison to cover up to a 24 cm × 16.4 cm field of view (FOV). We measured spatial resolution, uniformity, recovery coefficients (RC), and quantification using the system clinical software. Image linearity and coefficient of variation (CV) at the edge of the FOV were also characterized. Anecdotal examples of clinical patient data are presented. Spatial resolution is 2.4 mm FWHM for image planes parallel to the detector faces; background variability is 6%; quantification and RC varied within the FOV; positioning linearity began at ~ 13 mm from the edge of the detector housing; CV increased rapidly at the edge of the FOV due to limited sampling in these image planes.

  1. Dust Emission at 8 and 24 μ m as Diagnostics of H ii Region Radiative Transfer

    Energy Technology Data Exchange (ETDEWEB)

    Oey, M. S.; López-Hernández, J.; Kellar, J. A. [Department of Astronomy, University of Michigan, 311 West Hall, 1085 South University Avenue, Ann Arbor, MI, 48109-1107 (United States); Pellegrini, E. W. [Institut für Theoretische Astrophysik, Albert-Überle-Str. 2, D-69120 Heidelberg (Germany); Gordon, K. D.; Meixner, M.; Roman-Duval, J. [Space Telescope Science Institute, 3700 San Martin Drive, Baltimore, MD 21218 (United States); Jameson, K. E. [Astronomy Department and Laboratory for Millimeter-wave Astronomy, University of Maryland, College Park, MD 20742 (United States); Li, A. [Department of Physics and Astronomy, University of Missouri, Columbia, MO 65211 (United States); Madden, S. C. [Laboratoire AIM, CEA, Université Paris VII, IRFU/Service d’Astrophysique, Bat. 709, F-91191 Gif-sur-Yvette (France); Bot, C. [Observatoire Astronomique de Strasbourg, Université de Strasbourg, CNRS, UMR 7550, 11 Rue de l’Université, F-67000 Strasbourg (France); Rubio, M. [Departamento de Astronomía, Universidad de Chile, Casilla 36-D, Santiago (Chile); Tielens, A. G. G. M. [Leiden Observatory, Leiden University, P.O. Box 9513, NL-2300RA Leiden (Netherlands)

    2017-07-20

    We use the Spitzer Surveying the Agents of Galaxy Evolution (SAGE) survey of the Magellanic Clouds to evaluate the relationship between the 8 μ m polycyclic aromatic hydrocarbon (PAH) emission, 24 μ m hot dust emission, and H ii region radiative transfer. We confirm that in the higher-metallicity Large Magellanic Cloud, PAH destruction is sensitive to optically thin conditions in the nebular Lyman continuum: objects identified as optically thin candidates based on nebular ionization structure show six times lower median 8 μ m surface brightness (0.18 mJy arcsec{sup −2}) than their optically thick counterparts (1.2 mJy arcsec{sup −2}). The 24 μ m surface brightness also shows a factor of three offset between the two classes of objects (0.13 versus 0.44 mJy arcsec{sup −2}, respectively), which is driven by the association between the very small dust grains and higher density gas found at higher nebular optical depths. In contrast, PAH and dust formation in the low-metallicity Small Magellanic Cloud is strongly inhibited such that we find no variation in either 8 μ m or 24 μ m emission between our optically thick and thin samples. This is attributable to extremely low PAH and dust production together with high, corrosive UV photon fluxes in this low-metallicity environment. The dust mass surface densities and gas-to-dust ratios determined from dust maps using Herschel HERITAGE survey data support this interpretation.

  2. Remarkably Intense Emission from Ruthenium(II) Complexes with Multiple Borane Centers.

    Science.gov (United States)

    Nakagawa, Atsushi; Sakuda, Eri; Ito, Akitaka; Kitamura, Noboru

    2015-11-02

    The electrochemical, spectroscopic, and phophysical properties of a series of Ru(II) complexes having a triarylborane-appended 2,2'-bipyridine (bpy) ligand(s) (RuBbpys: [Ru(Bbpy)n(bpy)(3-n)](2+) (B1n) and [Ru(B2bpy)n(bpy)(3-n)](2+) (B2n), B = (dimesityl)boryldurylethynyl group(s) at the 4- or 4,4'-position(s) in bpy, n = 1-3) are described. In the excited states of the complexes, the intramolecular charge transfer transitions between the π-orbital of the aryl group and the vacant p-orbital on the boron atom (π(aryl)-p(B) CT) synergistically interact with the metal-to-ligand charge transfer (MLCT) transitions. The molar absorption coefficient of the MLCT band (ε(MLCT)) of the complex increased with increasing n, and B23 showed extremely intense absorption with ε(MLCT) = 5.6 × 10(4) M(-1) cm(-1) at 488 nm. Furthermore, B23 showed the highest emission quantum yield (0.43) among those of the polypyridine Ru(II) complexes hitherto reported. As one of the interesting results, we report that the radiative rate constant of B2n shows the correlation with ε(MLCT). The effects of the synergistic MLCT/π(aryl)-p(B) CT interactions on the spectroscopic and photophysical characteristics of RuBbpys are discussed in detail.

  3. On The gamma-ray emission from Reticulum II and other dwarf galaxies

    Energy Technology Data Exchange (ETDEWEB)

    Hooper, Dan; Linden, Tim

    2015-09-01

    The recent discovery of ten new dwarf galaxy candidates by the Dark Energy Survey (DES) and the Panoramic Survey Telescope and Rapid Response System (Pan-STARRS) could increase the Fermi Gamma-Ray Space Telescope's sensitivity to annihilating dark matter particles, potentially enabling a definitive test of the dark matter interpretation of the long-standing Galactic Center gamma-ray excess. In this paper, we compare the previous analyses of Fermi data from the directions of the new dwarf candidates (including the relatively nearby Reticulum II) and perform our own analysis, with the goal of establishing the statistical significance of any gamma-ray signal from these sources. We confirm the presence of an excess from Reticulum II, with a spectral shape that is compatible with the Galactic Center signal. The significance of this emission is greater than that observed from 99.84% of randomly chosen high-latitude blank-sky locations, corresponding to a local detection significance of 3.2σ. We caution that any dark matter interpretation of this excess must be validated through observations of additional dwarf spheroidal galaxies, and improved calculations of the relative J-factor of dwarf spheroidal galaxies. We improve upon the standard blank-sky calibration approach through the use of multi-wavelength catalogs, which allow us to avoid regions that are likely to contain unresolved gamma-ray sources.

  4. Copernicus observations of Ly-alpha and Mg II emission from HR 1099 /V711 Tauri/ and UX Ari

    Science.gov (United States)

    Weiler, E. J.

    1978-01-01

    Ultraviolet observations of two RS CVn binaries obtained with Copernicus are described. High-resolution (0.05 A) U1 observations indicate that both HR 1099 and UX Ari display broad Ly-alpha emission. The Ly-alpha emission strength from HR 1099 is variable and seems to be correlated with orbital phase, while the UX Ari results indicate no significant variation. Moderate resolution (0.51 A) V2 scans of both systems show variable Mg II h and k emission-line profiles which usually matched the velocity of the more active star in each binary. Additionally, displaced emission components were seen at velocities of up to + or - 250 km/s, indicative of high-velocity gas motions. The radial velocities of these emission features from HR 1099 are marginally correlated with orbital phase. Highly active and variable chromospheric phenomena are found to be the most consistent explanation of these results.

  5. Modifying Emission Spectral Bandwidth of Phosphorescent Platinum(II) Complexes Through Synthetic Control.

    Science.gov (United States)

    Li, Guijie; Wolfe, Alicia; Brooks, Jason; Zhu, Zhi-Qiang; Li, Jian

    2017-07-17

    The design, synthesis, and characterization of a series of tetradentate cyclometalated Pt(II) complexes are reported. The platinum complexes have the general structure Pt(ppz-O-CbPy-R), where a tetradentate cyclometalating ligand is consisting of ppz (3,5-dimethyl-1-phenyl-pyrazole), CbPy (carbazolylpyridine) components, and an oxygen bridging group. Variations of the R group on the pyridyl ring with various electron withdrawing and donating substituents are shown to have profound effects on the photophysical properties of Pt complexes. Electrochemical analysis indicates that reduction process occurs mainly on the electron-accepting pyridyl group, and the irreversible oxidation process is primarily localized on the metal-phenyl portions. The studies of their photophysical properties indicate that the lowest excited state of the platinum complexes is a ligand-centered 3 π-π* state with minor to significant 1 MLCT/ 3 MLCT character and are strongly dependent on the nature of the electron-accepting pyridyl moiety. A systematic study of the substituent effects on the pyridyl ring demonstrates that the T 1 state properties can be tuned by altering the functionality and positions of substituents. Importantly, it is revealed that how the emission spectra of the Pt(II) complexes can be significantly narrowed and why it can be achieved by incorporating an electron-donating group on the 4-position of the pyridyl ring. Most of the Pt(II) complexes reported here are highly emissive at room temperature in dichloromethane solutions (Φ = 1.1-95%) and in doped PMMA films (Φ = 29-88%) with luminescent lifetimes in the microsecond range (τ = 0.6-13.5 μs in solution and 0.9-11.3 μs in thin film respectively) and λ max = 442-568 nm and 440-544 nm in solution and thin film, respectively. Moreover, these complexes are neutral and thermally stable for sublimation, indicating that they can be useful for display and solid-state lighting applications.

  6. Designer ligands. Part 14. Novel Mn(lI), Ni(II) and Zn(II) complexes of benzamide- and biphenyl-derived ligands

    CSIR Research Space (South Africa)

    Wellington, Kevin W

    2009-01-01

    Full Text Available Manganese (II), nickel (II) and zinc (II) complexes have been prepared using various benzamideand biphenyl-derived ligands; their structures have been investigated using infrared spectroscopy and it is apparent that, depending on the ligand...

  7. 40 CFR Table 4 to Subpart Jjj of... - Class II Emission Limits for Existing Small Municipal Waste Combustion Unitsa

    Science.gov (United States)

    2010-07-01

    ... Small Municipal Waste Combustion Unitsa 4 Table 4 to Subpart JJJ of Part 62 Protection of Environment... Combustion Units Constructed on or Before August 30, 1999 Pt. 62, Subpt. JJJ, Table 4 Table 4 to Subpart JJJ of Part 62—Class II Emission Limits for Existing Small Municipal Waste Combustion Unitsa ER31JA03.009...

  8. Effect on the Inhibitory Activity of Potential Microbes on the Complexation of Methyl Anthranilate Derived Hydrazide with Cu, Ni and Zn (II) Metal Ions

    International Nuclear Information System (INIS)

    Ikram, M.; Rehman, S.; Khan, K.

    2013-01-01

    The hydrazide ligand 2-amino-(N-aminobezoyl)benzohydrazide (ABH) have been synthesized and characterized by 1H-NMR, 13C-NMR, ES+-MS, elemental analyses and infrared studies. The ligand was complexed with Ni(II), Cu(II) and Zn(II) metal ions and were characterized by analytical and spectroscopic methods including elemental analyses, ES+-MS, conductance, infrared, UV-Visible and magnetic susceptibilities studies. Infrared spectra show that the ligand form complexes through -NH2 and carbonyl moieties, the elemental studies suggested the M(ABH)X2 composition of the coordination compounds. The synthesized complexes were studied for their biological activities against gram negative bacteria including Escherichia coli, Salmonella typhi, Enterobacter aerogenes, Proteus vulgaris, Pseudomonas aeruginosa, Gram positive bacterial strains like Staphylococcus aureus and fungus like Candida albican. These activities show that the metal complexes are more active to the tested microbes as compared to neat ligand. (author)

  9. Detection of O I and Si II far-infrared fine-structure emission from Alpha Orionis

    Science.gov (United States)

    Haas, Michael R.; Glassgold, Alfred E.

    1993-01-01

    We have detected forbidden O I 63 micron and forbidden Si II 35 micron emission from the oxygen-rich, M2 lab supergiant, Alpha Orionis (Betelgeuse). The forbidden O I line flux is 2.4 +/- 0.2 x 10 exp -18 W/sq cm, and the forbidden Si II line flux is 0.9 +/- 0.4 x 10 exp -18 W/sq cm. These fluxes are consistent with the thermal model of Rodgers and Glassgold (1991), which indicates that the emission arises in dense, warm gas in Alpha Ori's inner envelope and implies that nearly all of the available O and Si is in atomic form. This is the first reported detection of FIR, fine-structure emission from the inner or transition region of a circumstellar envelope, where molecules and dust are expected to form.

  10. Transition probabilities for lines of Cr II, Na II and Sb I by laser produced plasma atomic emission spectroscopy; Probabilidades de transicion de algunos niveles de Cr II, Na II y Sb I medediante espectroscopia de plasma producidos por laser

    Energy Technology Data Exchange (ETDEWEB)

    Gonzalez, A. M.; Ortiz, M.; Campos, J.

    1995-07-01

    Absolute transition probabilities for lines of CR II, Na II and Sb I were determined by emission spectroscopy of laser induced plasmas. the plasma was produced focusing the emission of a pulsed Nd-Yag laser on solid samples containing the atom in study. the light arising from the plasma region was collected by and spectrometer. the detector used was a time-resolved optical multichannel analyzer (OMA III EG and G). The wavelengths of the measured transitions range from 2000 sto 4100 A. The spectral resolution of the system was 0. 2 A. The method can be used in insulators materials as Cl Na crystals and in metallic samples as Al-Cr and Sn-Sn alloys. to avoid self-absorption effects the alloys were made with low Sb or Cr content. Relative transition probabilities have been determined from measurements of emission-line intensities and were placed on an absolute scale by using, where possible, accurate experimental lifetime values form the literature or theoretical data. From these measurements, values for plasma temperature (8000-24000 K), electron densities ({approx}{approx} 10''16 cm ''-3) and self-absorption coefficients have been obtained. (Author) 56 refs.

  11. Synthesis and structure of 1,3-dimethyl-5-(p-sulfonamide-phenylazo)-6-aminouracil and its Ni(II) complex: Topological insights and investigation for noncovalent interactions

    Science.gov (United States)

    Debnath, Diptanu; Roy, Subhadip; Purkayastha, Atanu; Bauzá, Antonio; Choudhury, Rupasree; Ganguly, Rakesh; Frontera, Antonio; Misra, Tarun Kumar

    2017-08-01

    The azo-derivative, 1,3-dimethyl-5-(p-sulfonamide-phenylazo)-6-aminouracil (HL) containing 6-aminouracil (a biomolecule) and sulfonamide functionality (commonly found in sulfa-drugs), and its Ni(II) complex, NiIIL2 were synthesized. Single-crystal X-ray diffraction studies show that the ligand (HL) consists of an E conformation about the azo-linkage with a nearly planar geometry and the complex possesses distorted square planar geometry. The H-bonded underlying networks of HL and NiIIL2 were topologically classified revealing distinct topological types, namely tts and hxl, respectively. Moreover, topology of molecular packings in HL and NiIIL2 has also been discussed. Density functional theory (DFT) calculations, at the M06-2X/def2TZVP level of theory, are employed to characterize a great variety of non-covalent interactions that explicitly show the importance of antiparallel stacking interactions established by π--π+ interactions and H-bonds in the self-assembled dimmers in HL and lp-π/C-H⋯π interactions in NiIIL2. The results of NMR and UV-vis spectroscopies evidence that the ligand exists in hydrazone-imine-keto (B) tautomeric form in solution. The ligand absorption bands consist of the overlapping bands of π→π* and n→π* transitions. The complex experiences electronic transitions that consist of basically ILCT in character with some sort of participation of the atomic d-orbitals of the nickel. The pKa value of the ligand is found to be 4.09.

  12. Synthesis, experimental and DFT characterization of the 2-((E)-(2-[(E)-2,3-Dihydroxybenzylideneamino]-5-methylphenyl)iminiomethyl)-6-hydroxyphenolate and its Ni(II) and Cu(II) complexes

    Science.gov (United States)

    Beyramabadi, S. Ali; Esmaeili, Bahareh; Gharib, Azar; Khorsandi-Chenarboo, Mahdi; Morsali, Ali; Khashi, Maryam; Sanavi-Khoshnood, Razieh

    2017-10-01

    Herein, the 2-((E)-(2-[(E)-2,3-Dihydroxybenzylideneamino]-5-methylphenyl)iminiomethyl)-6-hydroxyphenolate dbnd H2L Schiff base and its Ni(II) and Cu(II) complexes were synthesized. In addition to experimental characterization, their optimized geometries, tautomerism of the H2L, assignment of the IR bands and NMR chemical shifts, Fukui functions and the Natural Bond Orbital (NBO) analysis were computed by employing the density functional theory (DFT) methods. The H2L salen-type Schiff base can exist as mixture of four possible tautomers, tautomerization of which has low barrier energy in methanol solution. For complexation, the H2L loses two phenolic protons to produce the L2- species, which acts as a dianionic tetradentate ligand. Based on the Fukui functions, the two deprotonated phenolic oxygens and two azomethine nitrogens are the four donating atoms and occupy the four coordination positions in the square-planar structure of the Ni(II) and Cu(II) complexes. In comparison with the its free form, the coordinated ligand shows a more planar structure in the optimized geometries of the complexes. The high-energy gaps of the frontier orbitals confirm that all three investigated compounds are stable.

  13. Adsorción de iones Ni(II sobre una arcilla bentonítica peletizada

    Directory of Open Access Journals (Sweden)

    Carlos Mejía Miranda

    2015-12-01

    Full Text Available La presencia de iones metálicos en aguas residuales genera un efecto tóxico para ecosistemas marinos y la salud pública. Las arcillas son materiales naturales con alta capacidad de adsorción y de bajo costo, viables para su implementación a nivel a industrial para la remoción de iones metálicos. Su implementación está limitada al desarrollo de alternativas para la utilización de estas arcillas a gran escala y en procesos continuos. La peletización de las arcillas permite su utilización en columnas de lecho fi jo. En este trabajo se evaluó la cinética de adsorción de iones níquel sobre una arcilla bentónica peletizada. Los extrudados se prepararon por humectación de la arcilla con una solución acidifi cada con ácido nítrico al 2%v. La proporción en volumen arcilla/solución acuosa fue 2:1. Se evaluó la remoción de iones níquel a 20, 40, 100 y 160 minutos y temperaturas de 25, 40 y 60°C. La cinética de adsorción de Ni(II se ajustó a un modelo de pseudo segundo orden. Las constantes cinéticas del modelo fueron 2,792x10-3, 8,085x10-4y 6,292x10-4g/mg.min para las temperaturas de reacción 25, 45 y 60°C, respectivamente. A partir de la lineación de la ecuación de Arrhenius se determinó la energía de activación y el factor de frecuencia para la reacción de adsorción de iones níquel sobre arcilla bentonítica, siendo 29,58kJ/moly 507,15g/mg.min, respectivamente. La magnitud de la energía de activación indica que la etapa controlante en la adsorción es la quimisorción de los iones níquel sobre la superfi cie de la arcilla.

  14. Removal, preconcentration and determination of Ni(II from different environmental samples using modified magnetite nanoparticles prior to flame atomic absorption spectrometry

    Directory of Open Access Journals (Sweden)

    Mohammad Ali Karimi

    2015-11-01

    Full Text Available In this paper, a simple, fast and reliable solid phase extraction (SPE method to determine Ni(II using dimethylglyoxim/sodium dodecyl sulfate-immobilized on alumina-coated magnetite nanoparticles (DMG/SDS-ACMNPs as a new adsorbent prior to its determination by flame atomic absorption spectrometry (FAAS is described. Under the optimal experimental conditions, the preconcentration factor, detection limit, linear range and relative standard deviation (RSD of nickel(II ions were 320 (for 800 mL of sample solution, 4.6 ng mL−1, 10.0–100.0 ng mL−1 and 1.9% (for 50.0 ng mL−1, n = 7, respectively. This method avoided the time-consuming column-passing process of loading large volume samples in traditional SPE through the rapid isolation of DMG/SDS-ACMNPs with an adscititious magnet. The proposed method was successfully applied to determine the content of Ni(II in soil, spinach, tomato, black tea, tobacco and different water samples and suitable recoveries were obtained.

  15. Effect of off-stoichiometry and site disorder on the properties of Ni3Al: II. Magnetics

    International Nuclear Information System (INIS)

    Abhyankar, A C; Semwal, A; Kaul, S N

    2008-01-01

    A detailed comparison between the magnetic behaviours of the 'as-prepared' ap-Ni x Al 100-x alloys with x = 74.3, 74.8, 75.1 and 76.1 at.% (that have both compositional disorder and site disorder) and 'annealed' counterparts (that have only compositional disorder) over a wide range of temperatures and magnetic fields (H) permits us to draw the following conclusions about the role of disorder. Regardless of the type of disorder, Curie temperature, T C , and spontaneous magnetization at 0 K, M 0 , decrease in accordance with the power laws T C (x) = t x (x-x c ) τ and M 0 (x) m x (x-x c ) ψ as x→x c (the threshold Ni concentration below which the long-range ferromagnetic order ceases to exist). Site disorder lowers the value of x c by nearly 1 at.% Ni, enhances T C for a given composition (more so as x→x c ) by increasing the number of Ni nearest neighbours for a given Ni atom, and leaves M 0 essentially unaltered because site disorder has essentially no effect on the density of states, N(E F ), at the Fermi level, E F , and the shape of the density-of-states curve near E F (except for x∼x c , where site disorder tends to primarily enhance N(E F ) and thereby stabilize long-range ferromagnetic order for Ni concentrations below the threshold concentration, x c ≅74.6 at.%, dictated by compositional disorder). At low and intermediate temperatures, spontaneous magnetization, M(T,H = 0), as well as the 'in-field' magnetization, M(T,H), exhibit non-Fermi liquid behaviour in the samples ap-Ni 74.3 and ap-Ni 74.8 . As x c is approached from above, i.e. as the compositional disorder increases, stronger deviations from the Fermi liquid behaviour occur and the temperature range over which the non-Fermi liquid behaviour persists widens. In contrast, the ap-Ni 75.1 and ap-Ni 76.1 alloys follow the behaviour that the self-consistent spin-fluctuation theory predicts for a weak itinerant-electron ferromagnet with no disorder. Both compositional disorder and site disorder

  16. Disorder and intermolecular interactions in a family of tetranuclear Ni(II) complexes probed by high-frequency electron paramagnetic resonance.

    Science.gov (United States)

    Lawrence, Jon; Yang, En-Che; Edwards, Rachel; Olmstead, Marilyn M; Ramsey, Chris; Dalal, Naresh S; Gantzel, Peter K; Hill, Stephen; Hendrickson, David N

    2008-03-17

    High-frequency electron paramagnetic resonance (HFEPR) data are presented for four closely related tetranuclear Ni(II) complexes, [Ni(hmp)(MeOH)Cl]4.H2O (1a), [Ni(hmp)(MeOH)Br]4.H2O (1b), [Ni(hmp)(EtOH)Cl]4.H2O (2), and [Ni(hmp)(dmb)Cl]4 (3) (where hmp(-) is the anion of 2-hydroxymethylpyridine and dmb is 3,3'-dimethyl-1-butanol), which exhibit magnetic bistability (hysteresis) and fast magnetization tunneling at low temperatures, properties which suggest they are single-molecule magnets (SMMs). The HFEPR spectra confirm spin S = 4 ground states and dominant uniaxial anisotropy (DSz(2), D SMM. The individual fine structure peaks (due to zero-field splitting) for complexes 1a, 1b, and 2 are rather broad. They also exhibit further (significant) splitting, which can be explained by the fact that there exists two crystallographically distinct Ni 4 sites in the lattices for these complexes, with associated differences in metal-ligand bond lengths and different zero-field splitting (ZFS) parameters. The broad EPR lines, meanwhile, may be attributed to ligand and solvent disorder, which results in additional distributions of microenvironments. In the case of complex 3, there are no solvate molecules in the structure, and only one distinct Ni 4 molecule in the lattice. Consequently, the HFEPR data for complex 3 are extremely sharp. As the temperature of a crystal of complex 3 is decreased, the HFEPR spectrum splits abruptly at approximately 46 K into two patterns with very slightly different ZFS parameters. Heat capacity data suggest that this is caused by a structural transition at 46.6 K. A single-crystal X-ray structure at 12(2) K indicates large thermal parameters on the terminal methyl groups of the dmb (3,3-dimethyl-1-butanol) ligand. Most likely there exists dynamic disorder of parts of the dmb ligand above 46.6 K; an order-disorder structural phase transition at 46.6 K then removes some of the motion. A further decrease in temperature (<6 K) leads to further fine

  17. Crystal structure, DNA binding, cleavage, antioxidant and antibacterial studies of Cu(II), Ni(II) and Co(III) complexes with 2-((furan-2-yl)methylimino)methyl)-6-ethoxyphenol Schiff base

    Science.gov (United States)

    Venkateswarlu, Kadtala; Kumar, Marri Pradeep; Rambabu, Aveli; Vamsikrishna, Narendrula; Daravath, Sreenu; Rangan, Krishnan; Shivaraj

    2018-05-01

    Three novel binary metal complexes; 1 [Cu(L)2], 2 [Ni(L)2] and 3 [Co(L)3] where, L (2-(((furan-2-yl) methylimino)methyl)-6-ethoxyphenol, C14H15NO3), were synthesized and characterized by various spectral techniques. Based on spectral studies square planar geometry is assigned for Cu(II) and Ni(II) complexes, whereas Co(III) owned octahedral geometry. Ligand, [Cu(L)2] and [Ni(L)2] are crystallized and found to be monoclinic crystal systems. CT-DNA absorption binding studies revealed that the complexes show good binding propensity (Kb = 5.02 × 103 M-1, 2.77 × 103 M-1, 1.63 × 104 M-1 for 1, 2 and 3 respectively). The role of these complexes in the oxidative and photolytic cleavage of supercoiled pBR322 DNA was studied and found that the complexes cleave the pBR322 DNA effectively. The catalytic ability of 1, 2 and 3 follows the order: 3 > 1 >2. Antioxidant studies of the new complexes revealed that they exhibit significant antioxidant activity against DPPH radical. The Schiff base and its metal complexes have been screened for antibacterial studies by Minimum Inhibitory Concentration method. It is observed that all metal complexes showed more activity than free ligand.

  18. Ni(ii) ions cleave and inactivate human alpha-1 antitrypsin hydrolytically, implicating nickel exposure as a contributing factor in pathologies related to antitrypsin deficiency.

    Science.gov (United States)

    Wezynfeld, Nina Ewa; Bonna, Arkadiusz; Bal, Wojciech; Frączyk, Tomasz

    2015-04-01

    Human alpha-1 antitrypsin (AAT) is an abundant serum protein present at a concentration of 1.0-1.5 g L(-1). AAT deficiency is a genetic disease that manifests with emphysema and liver cirrhosis due to the accumulation of a misfolded AAT mutant in hepatocytes. Lung AAT amount is inversely correlated with chronic obstructive pulmonary disease (COPD), a serious and often deadly condition, with increasing frequency in the aging population. Exposure to cigarette smoke and products of fossil fuel combustion aggravates AAT deficiency and COPD according to mechanisms that are not fully understood. Taking into account that these fumes contain particles that can release nickel to human airways and skin, we decided to investigate interactions of AAT with Ni(ii) ions within the paradigm of Ni(ii)-dependent peptide bond hydrolysis. We studied AAT protein derived from human blood using HPLC, SDS-PAGE, and mass spectrometry. These studies were aided by spectroscopic experiments on model peptides. As a result, we identified three hydrolysis sites in AAT. Two of them are present in the N-terminal part of the molecule next to each other (before Thr-13 and Ser-14 residues) and effectively form one N-terminal cleavage site. The single C-terminal cleavage site is located before Ser-285. The N-terminal hydrolysis was more efficient than the C-terminal one, but both abolished the ability of AAT to inhibit trypsin in an additive manner. Nickel ions bound to hydrolysis products demonstrated an ability to generate ROS. These results implicate Ni(ii) exposure as a contributing factor in AAT-related pathologies.

  19. A Comparison of Distortion Product Otoacoustic Emission Properties in Ménière's Disease Patients and Normal-Hearing Participants.

    Science.gov (United States)

    Drexl, Markus; Krause, Eike; Gürkov, Robert

    Postmortem examination of temporal bones of Ménière's disease patients consistently show dilated endolymphatic spaces of the inner ear, for which the term endolymphatic hydrops has been coined. During the past decade, magnetic resonance imaging techniques for the inner ear appeared, advancing the diagnosis of Ménière's disease. They require, however, a field-strength of at least 3 T, are costly and not universally available. Alternative, noninvasive, cost-effective tests with high sensitivity and specifity for endolymphatic hydrops are desirable. In this study, we test the suitability of distortion product otoacoustic emissions (DPOAEs) for endolymphatic hydrops detection. Previous measurements of the commonly recorded cubic DPOAEs mainly register cochlear hearing loss and are not specific for Ménière's disease. Simultaneous recordings of cubic and quadratic DPOAEs might be more suitable to detect endolymphatic hydrops, because both DPOAE orders react differently to changes of the cochlear operating point as they might occur in Ménière's disease patients. Cubic and quadratic DPOAEs were recorded in normal-hearing participants (N = 45) and in the affected and unaffected ears of patients with a diagnosis of definite Ménière's disease (N = 32). First, to assess the integrity of DPOAE-generating mechanisms, cubic DPOAE-grams were obtained with primary tone frequencies f2 between 1 and 8 kHz with primary tone levels l1 = 60 dB SPL and l2 = 50 dB SPL, and a fixed primary tone frequency ratio of 1.22. Then, cubic and quadratic DPOAEs were simultaneously recorded with primary tone levels l1 = l2 = 65 dB SPL and at primary tone frequencies f2 = 4 and 5 kHz, where f1 was successively varied such that the ratio f2/f1 ranged between 1.1 and 1.6 in 0.04 steps while quadratic and cubic DPOAE levels were extracted from the same recording. Cubic DPOAEs were significantly reduced in the affected ears of Ménière's disease patients, and slightly reduced in the

  20. Preparation and use of samarium diiodide (SmI(2)) in organic synthesis: the mechanistic role of HMPA and Ni(II) salts in the samarium Barbier reaction.

    Science.gov (United States)

    Sadasivam, Dhandapani V; Choquette, Kimberly A; Flowers, Robert A

    2013-02-04

    Although initially considered an esoteric reagent, SmI(2) has become a common tool for synthetic organic chemists. SmI(2) is generated through the addition of molecular iodine to samarium metal in THF.(1,2-3) It is a mild and selective single electron reductant and its versatility is a result of its ability to initiate a wide range of reductions including C-C bond-forming and cascade or sequential reactions. SmI(2) can reduce a variety of functional groups including sulfoxides and sulfones, phosphine oxides, epoxides, alkyl and aryl halides, carbonyls, and conjugated double bonds.(2-12) One of the fascinating features of SmI-(2)-mediated reactions is the ability to manipulate the outcome of reactions through the selective use of cosolvents or additives. In most instances, additives are essential in controlling the rate of reduction and the chemo- or stereoselectivity of reactions.(13-14) Additives commonly utilized to fine tune the reactivity of SmI(2) can be classified into three major groups: (1) Lewis bases (HMPA, other electron-donor ligands, chelating ethers, etc.), (2) proton sources (alcohols, water etc.), and (3) inorganic additives (Ni(acac)(2), FeCl(3), etc).(3) Understanding the mechanism of SmI(2) reactions and the role of the additives enables utilization of the full potential of the reagent in organic synthesis. The Sm-Barbier reaction is chosen to illustrate the synthetic importance and mechanistic role of two common additives: HMPA and Ni(II) in this reaction. The Sm-Barbier reaction is similar to the traditional Grignard reaction with the only difference being that the alkyl halide, carbonyl, and Sm reductant are mixed simultaneously in one pot.(1,15) Examples of Sm-mediated Barbier reactions with a range of coupling partners have been reported,(1,3,7,10,12) and have been utilized in key steps of the synthesis of large natural products.(16,17) Previous studies on the effect of additives on SmI(2) reactions have shown that HMPA enhances the

  1. Advanced Diagnostics for the Study of Linearly Polarized Emission. II. Application to Diffuse Interstellar Radio Synchrotron Emission

    Science.gov (United States)

    Herron, C. A.; Burkhart, Blakesley; Gaensler, B. M.; Lewis, G. F.; McClure-Griffiths, N. M.; Bernardi, G.; Carretti, E.; Haverkorn, M.; Kesteven, M.; Poppi, S.; Staveley-Smith, L.

    2018-03-01

    Diagnostics of polarized emission provide us with valuable information on the Galactic magnetic field and the state of turbulence in the interstellar medium, which cannot be obtained from synchrotron intensity alone. In Paper I, we derived polarization diagnostics that are rotationally and translationally invariant in the Q–U plane, similar to the polarization gradient. In this paper, we apply these diagnostics to simulations of ideal magnetohydrodynamic turbulence that have a range of sonic and Alfvénic Mach numbers. We generate synthetic images of Stokes Q and U for these simulations for the cases where the turbulence is illuminated from behind by uniform polarized emission and where the polarized emission originates from within the turbulent volume. From these simulated images, we calculate the polarization diagnostics derived in Paper I for different lines of sight relative to the mean magnetic field and for a range of frequencies. For all of our simulations, we find that the polarization gradient is very similar to the generalized polarization gradient and that both trace spatial variations in the magnetoionic medium for the case where emission originates within the turbulent volume, provided that the medium is not supersonic. We propose a method for distinguishing the cases of emission coming from behind or within a turbulent, Faraday rotating medium and a method to partly map the rotation measure of the observed region. We also speculate on statistics of these diagnostics that may allow us to constrain the physical properties of an observed turbulent region.

  2. Asymmetric synthesis of chiral heterocyclic amino acids via the alkylation of the Ni(II) complex of glycine and alkyl halides.

    Science.gov (United States)

    Chen, Hui; Wang, Jiang; Zhou, Shengbin; Liu, Hong

    2014-09-05

    An investigation into the reactivity profile of alkyl halides has led to the development of a new method for the asymmetric synthesis of chiral heterocyclic amino acids. This protocol involves the asymmetric alkylation of the Ni(II) complex of glycine to form an intermediate, which then decomposes to form a series of valuable chiral amino acids in high yields and with excellent diastereoselectivity. The chiral amino acids underwent a smooth intramolecular cyclization process to afford the valuable chiral heterocyclic amino acids in high yields and enantioselectivities. This result paves the way for the development of a new synthetic method for chiral heterocyclic amino acids.

  3. Anion controlled structural and magnetic diversity in unusual mixed-bridged polynuclear Ni(II) complexes with a versatile bis(2-methoxy phenol)diamine hexadentate ligand. An experimental and theoretical magneto-structural study.

    Science.gov (United States)

    Botana, Luis; Ruiz, José; Mota, Antonio J; Rodríguez-Diéguez, Antonio; Seco, José M; Oyarzabal, Itziar; Colacio, Enrique

    2014-09-28

    This work reports the syntheses, crystal structures, magnetic properties and DFT calculations of six novel polynuclear NiII compounds [Ni2(μ-HL1)2(μ-N3)]N3·(CH3OH)2·2H2O (1), [Ni2(μ-HL1)2(μ-N3)][Na2Ni2(μ-L1)2(μ-N3)2(CH3OH)(N3)]·4CH3OH (2), [Ni4(μ-L1)2(μ-N3)4(CH3OH)2]·2CH3OH (3), [Na2Ni4(μ-L1)2(μ-OAc)2(μ-N3)4(CH3OH)4]·2CH3OH (4), [Ni4(μ-L1)2(μ-Cl)2(Cl)2] (5), and [Ni3(μ-L1)2(acac)2(H2O)2] (6), with uncommon structures and rare mixed-bridges between NiII ions, which were prepared from the versatile polytopic Mannich base ligand N,N′-dimethyl-N,N′-bis(2-hydroxy-3-methoxy-5-methylbenzyl)ethylenediamine (H2L1). The anionic coligand (azide, chloride, acetate and acetylacetonate) and reaction conditions play crucial roles in determining the final structure of these compounds and consequently their magnetic properties. Compound 1 contains a Ni2 cationic unit with rare di-μ-phenoxido/μ1,1-azide triple mixed bridges whereas complex 2 is made from the same Ni2 cationic unit as 1, cocrystallized with Na2Ni2 neutral units, in which double μ1,1,1-azide bridges connect the NiII and NaI anions. Complexes 3 and 4 are Ni4 complexes with defective dicubane and linear structures, respectively. Complex 3 has two distinct types of mixed bridges, μ-phenoxido/μ1,1,1-azido and μ1,1-azido/μ1,1,1-azido and a double di-μ1,1,1-azido bridge, the latter connecting the face-sharing NiII ions. In 4, rare μ-phenoxido/μ1,1-azide/syn–syn acetate triple mixed bridges connect central and terminal NiII atoms whereas a double μ1,1-azide planar bridging fragment links the central NiII ions. Complex 5 has a defective-dicubane structure with double μ-phenoxido/μ3-chloro mixed bridges and di-μ3-chloro bridges, whereas complex 6 has a bent structure with very uncommon single μ-phenoxido bridges. The analysis of the magnetic properties reveals that in complexes 1–4 all magnetic pathways transmit ferromagnetic interactions leading to S = 2 ground states for 1 and 2 and

  4. Influence of Co-Doping of Ni (II on Photocatalytic Activity of TiO2 for Pathogenic Bacteria Inhibition

    Directory of Open Access Journals (Sweden)

    Baharuddin Shaleh

    2010-04-01

    Full Text Available Nanoparticle titanium dioxide (TiO2 has most attention in the past decade, since it can be applied as alternative material on sterilization photocatalyst process. This research focused on increasing performance of titania such as structure, particles size and surface area through Ni ion doped on TiO2 surface by sol-gel technique. Product were used to design of a photobioreactor for sterilization process from pathogenic bacteria such as Escherichia coli, Staphylococcus aureus and Bacillus subtilis. Product were characterized using TG-DTA, XRD, TEM, SEM-EDS and BET. Titanium dioxide with anatase structure have 12.1 nm in particles size and surface area 49.6 m2/ g that have higher inhibition rate to bacteria cell. Photobiocatalytic reaction was carried out in various TiO2-Ni concentration and UV irradiation times. The anti bacteria from TiO2-Ni to all bacteria cell suspension after UV irradiated at λm : 365 nm has good synergistic effect. Effect of mechanical treatment by sonicator showed the increasing inhibition rate around 4% for 120 minute irradiation. Inhibition rate optimization for each bacteria gave different efficiency inhibition to TiO2-Ni concentration 1.5-2.0 g/L. TiO2-Ni inhibited growth of Escherichia coli, Staphylococcus aureus around ≥ 95% for 120 minute irradiation, while Bacillus subtilis resistance with inhibition percentage rate only 88.1%.

  5. A novel dinuclear Ru(II) complex having a bridging ligand of a rigid and extended structure. Incorporation of an anthraquinone unit and efficient emission quenching

    International Nuclear Information System (INIS)

    Mishra, L.; Choi, Chang-Shik; Araki, Koji

    1997-01-01

    Dinuclear Ru(II) complex having extended conjugation within the bridging ligand was prepared by coupling of the Ru(II) polypyridyl complex having a benzoyl-substituted phenazine unit with diaminoanthraquinone in one step, in which emission from the excited Ru(II) center was efficiently quenched through the anthraquinone unit. (author)

  6. Crystal structure of calcium dinickel(II iron(III tris(orthophosphate: CaNi2Fe(PO43

    Directory of Open Access Journals (Sweden)

    Said Ouaatta

    2017-06-01

    Full Text Available The title compound, CaNi2Fe(PO43, was synthesized by solid-state reactions. Its structure is closely related to that of α-CrPO4 in the space group Imma. Except for two O atoms in general positions, all atoms are located in special positions. The three-dimensional framework is built up from two types of sheets extending parallel to (100. The first sheet is made up from two edge-sharing [NiO6] octahedra, leading to the formation of [Ni2O10] double octahedra that are connected to two PO4 tetrahedra through a common edge and corners. The second sheet results from rows of corner-sharing [FeO6] octahedra and PO4 tetrahedra forming an infinite linear chain. These layers are linked together through common corners of PO4 tetrahedra and [FeO6] octahedra, resulting in an open three-dimensional framework that delimits two types of channels parallel to [100] and [010] in which the eightfold-coordinated CaII cations are located.

  7. A Hirshfeld surface analysis, synthesis, structure and characterization of a new Ni(II) diamagnetic complex with the bidentate ligand homopiperazine

    Science.gov (United States)

    Klai, Kacem; Kaabi, Kamel; Jelsch, Christian; Wenger, Emmanuel; Lefebvre, Frédéric; Ben Nasr, Cherif

    2017-11-01

    A new Ni(II) complex with the bidentate ligand homopiperazine, [Ni(C5H12N2)2](CH3COO)2.4H2O, has been prepared and characterized by single crystal X-ray diffraction, elemental analysis and IR spectroscopy. The basic coordination patterns of the homopiperazine coordinated metal cations are slightly distorted square planar. In the atomic arrangement, the cationic complexes [Ni(C5H12N2)2]2+ are interconnected by the CH3COO-anions via Nsbnd H⋯O and Csbnd H⋯O hydrogen bonds to form layers parallel to the (a, b) plane. These layers are connected by hydrogen bonds generated with water molecules to build a three dimensional network. The charge density of the compound could be refined from X-ray diffraction data measured at cryogenic temperature. Intermolecular interactions were investigated by Hirshfeld surfaces. The title compound is diamagnetic as confirmed by theoretical calculations, allowing its 13C and 15N solid-state NMR spectra to be recorded. Absorption bands were identified by infrared spectroscopy. Electronic properties such as HOMO and LUMO energies were also obtained.

  8. Two new Ni(II) supramolecular complexes based on ethyl isonicotinate and ethyl nicotinate for removal of acid blue 92 dye

    Science.gov (United States)

    Etaiw, Safaa El-din H.; Marie, Hassan

    2018-03-01

    Two new luminescent supramolecular complexes (SC); [Ni(EIN)4(NCS)2] SC1 and [Ni2(EN)8(NCS)4] SC2, (EIN = ethyl isonicotinate, EN = ethyl nicotinate), have been synthesized by self-assembly method and structurally characterized by X-ray single crystal, FT-IR and UV-Vis spectra, PXRD, elemental and thermogravimetric analyses. Both SC1 and SC2 are monoclinic crystals however, they have different asymmetric units. Ni(II) atoms in both SC are isostructural and have similar hexa-coordinate environment. The structures of SC1 and SC2 consist of parallel polymeric 1D-chains, extended in two and three dimensional supramolecular frameworks by intermolecular hydrogen bonding interactions. SC1 and SC2 are luminescent materials which can be used in applications as molecular sensing systems. SC1 and SC2 were used as heterogeneous catalysts for degradation of acid blue 92 (AB-92) under sun light irradiation. The fluorescence measurements of terephthalic acid technique as a probe molecule were used to determine the •OH radicals. Also the radicals trapping experiments using isopropanol alcohol (IPA) as radical scavenger were discussed. In addition a mechanism of degradation was proposed and discussed.

  9. Simultaneous removal of Ni(II), As(III), and Sb(III) from spiked mine effluent with metakaolin and blast-furnace-slag geopolymers.

    Science.gov (United States)

    Luukkonen, Tero; Runtti, Hanna; Niskanen, Mikko; Tolonen, Emma-Tuulia; Sarkkinen, Minna; Kemppainen, Kimmo; Rämö, Jaakko; Lassi, Ulla

    2016-01-15

    The mining industry is a major contributor of various toxic metals and metalloids to the aquatic environment. Efficient and economical water treatment methods are therefore of paramount importance. The application of natural or low-cost sorbents has attracted a great deal of interest due to the simplicity of its process and its potential effectiveness. Geopolymers represent an emerging group of sorbents. In this study, blast-furnace-slag and metakaolin geopolymers and their raw materials were tested for simultaneous removal of Ni(II), As(III) and Sb(III) from spiked mine effluent. Blast-furnace-slag geopolymer proved to be the most efficient of the studied materials: the experimental maximum sorption capacities for Ni, As and, Sb were 3.74 mg/g, 0.52 mg/g, and 0.34 mg/g, respectively. Although the capacities were relatively low due to the difficult water matrix, 90-100% removal of Ni, As, and Sb was achieved when the dose of sorbent was increased appropriately. Removal kinetics fitted well with the pseudo-second-order model. Our results indicate that geopolymer technology could offer a simple and effective way to turn blast-furnace slag to an effective sorbent with a specific utilization prospect in the mining industry. Copyright © 2015 Elsevier Ltd. All rights reserved.

  10. Synthesis and Characterization of Cu(II), Co(II) and Ni(II) Complexes of Trithiocyanuric Acid: The Structure of {N,N'-Bis(3-Aminopropyl)-1,3-Propanediamine}-(Trithiocyanurato)Nickel(II)

    Czech Academy of Sciences Publication Activity Database

    Kopel, P.; Trávníček, Zdeněk; Kvítek, L.; Černošek, Z.; Wrzeszcz, G.; Marek, J.

    2003-01-01

    Roč. 56, č. 1 (2003), s. 1-11 ISSN 0095-8972 R&D Projects: GA ČR GA203/00/0152; GA AV ČR IBS5038351 Institutional research plan: CEZ:AV0Z5038910 Keywords : Copper(II) * cobalt(II) and nickel(II) complexes * Trithiocyanuric acid Subject RIV: CE - Biochemistry Impact factor: 0.841, year: 2003

  11. Aspartic acid interaction with cobalt(II) in dilute aqueous solution: A 57Co emission Mössbauer spectroscopic study

    International Nuclear Information System (INIS)

    Kamnev, Alexander A.; Tugarova, Anna V.; Kovács, Krisztina; Homonnay, Zoltan; Kuzmann, Erno; Vértes, Attila

    2012-01-01

    Emission ( 57 Co) Mössbauer spectra of the aspartic acid— 57 CoCl 2 system were measured at T = 80 K in frozen aqueous solution and in the form of a dried residue of this solution. The Mössbauer spectra, besides a weak contribution from after-effects, showed two Fe 2 +  /Co 2 +  components which were ascribed to octahedrally and tetrahedrally coordinated 57 Co II microenvironments in the Asp–cobalt(II) complex. This dual coordination mode may be due to the involvement of the second terminal carboxylic group of aspartic acid in the coordination sphere of Co.

  12. Rotation and kinematics of the premain-sequence stars in Taurus-Auriga with Ca II emission

    Science.gov (United States)

    Hartmann, Lee W.; Soderblom, David R.; Stauffer, John R.

    1987-01-01

    Radial velocities and v sin i values for the stars in the Taurus-Auriga region that were found to have strong Ca II H and K emission by Herbig, Vrba, and Rydgren 'HVR', (1986) are reported. Most of the velocities are determined to better than 2 km/s precision. The kinematic properties of the Ca II emission stars with strong Li are found to be indistinguishable from conventional T Tauris in Taurus-Auriga, contrary to HVR. These Li-rich stars also rotate like T Tauris. Most of the stars that lack Li are probable or possible members of the Hyades, in the foreground, and are among the brightest and most active stars in that cluster for their spectral types. It is suggested following Jones and Herbig (1979), that the apparent absence of low-mass stars older than 10 Myr in Taurus-Auriga is real, and is due to the finite lifetime of the cloud.

  13. Rotation and kinematics of the premain-sequence stars in Taurus-Auriga with CA II emission

    Science.gov (United States)

    Hartmann, Lee W.; Soderblom, David R.; Stauffer, John R.

    1987-04-01

    The authors report radial velocities and v sin i values for the stars in the Taurus-Auriga region that were found to have strong Ca II H and K emission by Herbig, Vrba, and Rydgren (HVR). Most of the velocities are determined to better than 2 km s-1 precision. The authors find the kinematic properties of the Ca II emission stars with strong Li to be indistinguishable from conventional T Tauris in Taurus-Auriga, contrary to HVR. These Li-rich stars also rotate like T Tauris. Most of the stars that lack Li are probable or possible members of the Hyades, in the foreground, and are among the brightest and most active stars in that cluster for their spectral types. The authors suggest, following Jones and Herbig, that the apparent absence of low-mass stars older than 10 Myr in Taurus-Auriga is real, and is due to the finite lifetime of the cloud.

  14. Experimental study of mixed additive of Ni(II) and piperazine on ammonia escape in CO2 capture using ammonia solution

    International Nuclear Information System (INIS)

    Ma, Shuangchen; Chen, Gongda; Zhu, Sijie; Wen, Jiaqi; Gao, Ran; Ma, Lan; Chai, Jin

    2016-01-01

    Highlights: • Compound additive was used to obtain high CO 2 absorption efficiency and low NH 3 escape. • Both organic material and metal ion were applied as compound additive. • Influences of additives on CO 2 absorption and NH 3 escape were investigated. • Possible mechanism and products were analyzed by XRD and UV–visible spectrophotometer. - Abstract: In order to obtain high CO 2 absorption efficiency and low ammonia escape rate, mixed additives of piperazine and Ni(II) were used as absorbent in bubbling reactor. The effects of mixed additive on CO 2 absorption efficiency and ammonia escape rate were investigated; the performances of mixed additive in removal process were compared with that of pure ammonia solution. The proposed mechanism was analyzed by XRD and UV–visible spectrophotometer. The mixed additive has well effect on CO 2 absorption efficiency and ammonia escape reduction. The CO 2 absorption efficiency was 72% when 2 wt% ammonia solution mixed with 0.025 mol/L piperazine and 0.05 mol/L Ni(II), higher than that achieved by 3 wt% ammonia solution without additive, and the amount of ammonia loss was nearly 1/3 compared with 3 wt% pure ammonia solution. This paper provided one feasible method which is beneficial to the balance between CO 2 absorption and ammonia escape in CO 2 capture process.

  15. Importance of nanoparticle size in colorimetric and SERS-based multimodal trace detection of Ni(II) ions with functional gold nanoparticles.

    Science.gov (United States)

    Krpetić, Zeljka; Guerrini, Luca; Larmour, Iain A; Reglinski, John; Faulds, Karen; Graham, Duncan

    2012-03-12

    Colorimetric detection of analytes using gold nanoparticles along with surface-enhanced Raman spectroscopy (SERS) are areas of intense research activity since they both offer sensing of very low concentrations of target species. Multimodal detection promotes the simultaneous detection of a sample by a combination of different techniques; consequently, surface chemistry design in the development of multimodal nanosensors is important for rapid and sensitive evaluation of the analytes by diverse analytical methods. Herein it is shown that nanoparticle size plays an important role in the design of functional nanoparticles for colorimetric and SERS-based sensing applications, allowing controlled nanoparticle assembly and tunable sensor response. The design and preparation of robust nanoparticle systems and their assembly is reported for trace detection of Ni(II) ions as a model system in an aqueous solution. The combination of covalently attached nitrilotriacetic acid moieties along with the L-carnosine dipeptide on the nanoparticle surface represents a highly sensitive platform for rapid and selective detection of Ni(II) ions. This systematic study demonstrates that significantly lower detection limits can be achieved by finely tuning the assembly of gold nanoparticles of different core sizes. The results clearly demonstrate the feasibility and usefulness of a multimodal approach. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Dye-doped nanostructure polypyrrole film for electrochemically switching solid-phase microextraction of Ni(II) and ICP-OES analysis of waste water.

    Science.gov (United States)

    Shamaeli, Ehsan; Alizadeh, Naader

    2012-01-01

    A nanostructure fiber based on conducting polypyrrole synthesized by an electrochemical method has been developed, and used for electrochemically switching solid-phase microextraction (ES-SPME). The ES-SPME was prepared by the doping of eriochrome blue in polypyrrole (PPy-ECB) and used for selectively extracting the Ni(II) cation in the presence of some transition and heavy metal ions. The cation-exchange behavior of electrochemically prepared polypyrrole on stainless-steel with and without eriochrome blue (ECB) dye was characterized using ICP-OES analysis. The effects of the scan rate for electrochemical synthesis, uptake and the release potential on the extraction behavior of the PPy-ECB conductive fiber were studied. Uptake and release time profiles show that the process of electrically switched cation exchange could be completed within 250 s. The results of the present study point concerning the possibility of developing a selective extraction process for Ni(II) from waste water was explored using such a nanostructured PPy-ECB film through an electrically switched cation exchange. 2012 © The Japan Society for Analytical Chemistry

  17. Biodiesel production from tall oil with synthesized Mn and Ni based additives: effects of the additives on fuel consumption and emissions

    Energy Technology Data Exchange (ETDEWEB)

    Ali Keskin; Metin Guru; Duran Altiparmak [Mersin University, Mersin (Turkey). Technical Education Faculty

    2007-05-15

    In this study, biodiesel fuel and fuel additives were produced from crude tall oil that is a by-product in the pulp manufacturing by craft or sulphate pulping process. Fatty acids and resinic acids were obtained from crude tall oil by distillation method. Tall oil methyl ester (biodiesel) was produced from fatty acids. Resinic acids were reacted with NiO and MnO{sub 2} stoichiometrically for production of metallic fuel additives. Each metallic fuel additive was added at the rate of 8 {mu}mol/l and 12 {mu}mol/l to make mixtures of 60% tall oil methyl ester/40% diesel fuel (TE60) for preparing test fuels. Metallic fuel additives improved properties of biodiesel fuels, such as pour point and viscosity values. Biodiesel fuels were tested in an unmodified direct injection diesel engine at full load condition. Specific fuel consumption of biodiesel fuels increased by 6.00%, however, in comparison with TE60, it showed trend of decreasing with adding of additives. Exhaust emission profile of biodiesel fuels improved. CO emissions and smoke opacity decreased up to 64.28% and 30.91% respectively. Low NOx emission was also observed in general for the biodiesel fuels. 28 refs., 4 figs., 3 tabs.

  18. Mathematical Modeling and a Hybrid NSGA-II Algorithm for Process Planning Problem Considering Machining Cost and Carbon Emission

    Directory of Open Access Journals (Sweden)

    Jin Huang

    2017-09-01

    Full Text Available Process planning is an important function in a manufacturing system; it specifies the manufacturing requirements and details for the shop floor to convert a part from raw material to the finished form. However, considering only economical criterion with technological constraints is not enough in sustainable manufacturing practice; formerly, criteria about low carbon emission awareness have seldom been taken into account in process planning optimization. In this paper, a mathematical model that considers both machining costs reduction as well as carbon emission reduction is established for the process planning problem. However, due to various flexibilities together with complex precedence constraints between operations, the process planning problem is a non-deterministic polynomial-time (NP hard problem. Aiming at the distinctive feature of the multi-objectives process planning optimization, we then developed a hybrid non-dominated sorting genetic algorithm (NSGA-II to tackle this problem. A local search method that considers both the total cost criterion and the carbon emission criterion are introduced into the proposed algorithm to avoid being trapped into local optima. Moreover, the technique for order preference by similarity to an ideal solution (TOPSIS method is also adopted to determine the best solution from the Pareto front. Experiments have been conducted using Kim’s benchmark. Computational results show that process plan schemes with low carbon emission can be captured, and, more importantly, the proposed hybrid NSGA-II algorithm can obtain more promising optimal Pareto front than the plain NSGA-II algorithm. Meanwhile, according to the computational results of Kim’s benchmark, we find that both of the total machining cost and carbon emission are roughly proportional to the number of operations, and a process plan with less operation may be more satisfactory. This study will draw references for the further research on green

  19. Clinical imaging characteristics of the positron emission mammography camera: PEM Flex Solo II.

    Science.gov (United States)

    MacDonald, Lawrence; Edwards, John; Lewellen, Thomas; Haseley, David; Rogers, James; Kinahan, Paul

    2009-10-01

    We evaluated a commercial positron emission mammography (PEM) camera, the PEM Flex Solo II. This system comprises two 6 x 16.4 cm detectors that scan together covering up to a 24 x 16.4 cm field of view (FOV). There are no specific standards for testing this detector configuration. We performed several tests important to breast imaging, and we propose tests that should be included in standardized testing of PEM systems. We measured spatial resolution, uniformity, counting- rate linearity, recovery coefficients, and quantification accuracy using the system's software. Image linearity and coefficient of variation at the edge of the FOV were also characterized. Anecdotal examples of clinical patient data are presented. The spatial resolution was 2.4 mm in full width at half maximum for image planes parallel to the detector faces. The background variability was approximately 5%, and quantification accuracy and recovery coefficients varied within the FOV. Positioning linearity began at approximately 13 mm from the edge of the detector housing. The coefficient of variation was significantly higher close to the edge of the FOV because of limited sensitivity in these image planes. A reconstructed spatial resolution of 2.4 mm represented a significant improvement over conventional whole-body PET scanners and should reduce the lower threshold on lesion size and tracer uptake for detection in the breast. Limited-angle tomography and a lack of data corrections result in spatially variable quantitative results. PEM acquisition geometry limits sampling statistics at the chest-wall edge of the camera, resulting in high variance in that portion of the image. Example patient images demonstrate that lesions can be detected at the chest-wall edge despite variance artifacts, and fine structure is visualized routinely throughout the FOV in the focal plane. The PEM Flex camera should enable the functional imaging of breast cancer earlier in the disease process than whole-body PET.

  20. Synthetic, structural, electrochemical and solvent extraction studies of neutral trinuclear Co(II), Ni(II), Cu(II) and Zn(II) metallocycles and tetrahedral tetranuclear Fe(III) species incorporating 1,4-aryl-linked bis-beta-diketonato ligands.

    Science.gov (United States)

    Clegg, Jack K; Bray, David J; Gloe, Kerstin; Gloe, Karsten; Jolliffe, Katrina A; Lawrance, Geoffrey A; Lindoy, Leonard F; Meehan, George V; Wenzel, Marco

    2008-03-14

    Uncharged complexes, formulated as trimeric metallocycles of type [M3(L(1))3(Py)6] (where M = cobalt(II), nickel(II) and zinc(II) and L(1) is the doubly deprotonated form of a 1,4-phenylene linked bis-beta-diketone ligand of type 1,4-bis(RC(O)CH2C(O))C6H4 (R = t-Bu)) have been synthesised, adding to related, previously reported complexes of these metals with L(1) (R = Ph) and copper(ii) with L(1) (R = Me, Et, Pr, t-Bu, Ph). New lipophilic ligand derivatives with R = hexyl, octyl or nonyl were also prepared for use in solvent extraction experiments. The X-ray structures of H2L(1) (R = t-Bu) and of its trinuclear (triangular) nickel(II) complex [Ni3(L(1))3(Py)6].3.5Py (R = t-Bu) are also presented. Electrochemical studies of H2L(1), [Co3(L(1))3(Py)6], [Ni3(L(1))3(Py)6], [Cu3(L(1))3], [Zn3(L(1))3(Py)6] and [Fe4(L(1))6] (all with R = t-Bu) show that oxidative processes for the complexes are predominantly irreversible, but several examples of quasireversible behaviour also occur and support the assignment of an anodic process, seen between +1.0 and +1.6 V, as involving metal-centred oxidations. The reduction behaviour for the respective metal complexes is not simple, being irreversible in most cases. Solvent extraction studies (water/chloroform) involving the systematic variation of the metal, bis-beta-diketone and heterocyclic base concentrations have been performed for cobalt(II) and zinc(II) using a radiotracer technique in order to probe the stoichiometries of the respective extracted species. Significant extraction synergism was observed when 4-ethylpyridine was also present with the bis-beta-diketone ligand in the chloroform phase. Competitive extraction studies demonstrated a clear uptake preference for copper(II) over cobalt(II), nickel(II), zinc(II) and cadmium(II).

  1. Choice of precipitant and calcination temperature of precursor for synthesis of NiCo2O4 for control of CO-CH4 emissions from CNG vehicles.

    Science.gov (United States)

    Trivedi, Suverna; Prasad, Ram

    2018-03-01

    Compressed natural gas (CNG) is most appropriate an alternative of conventional fuel for automobiles. However, emissions of carbon-monoxide and methane from such vehicles adversely affect human health and environment. Consequently, to abate emissions from CNG vehicles, development of highly efficient and inexpensive catalysts is necessary. Thus, the present work attempts to scan the effects of precipitants (Na 2 CO 3 , KOH and urea) for nickel cobaltite (NiCo 2 O 4 ) catalysts prepared by co-precipitation from nitrate solutions and calcined in a lean CO-air mixture at 400°C. The catalysts were used for oxidation of a mixture of CO and CH 4 (1:1). The catalysts were characterized by X-ray diffractometer, Brunauer-Emmett-Teller surface-area, X-ray photoelectron spectroscopy; temperature programmed reduction and Scanning electron microscopy coupled with Energy-Dispersive X-Ray Spectroscopy. The Na 2 CO 3 was adjudged as the best precipitant for production of catalyst, which completely oxidized CO-CH 4 mixture at the lowest temperature (T 100 =350°C). Whereas, for catalyst prepared using urea, T 100 =362°C. On the other hand the conversion of CO-CH 4 mixture over the catalyst synthesized by KOH limited to 97% even beyond 400°C. Further, the effect of higher calcination temperatures of 500 and 600°C was examined for the best catalyst. The total oxidation of the mixture was attained at higher temperatures of 375 and 410°C over catalysts calcined at 500 and 600°C respectively. Thus, the best precipitant established was Na 2 CO 3 and the optimum calcination temperature of 400°C was found to synthesize the NiCo 2 O 4 catalyst for the best performance in CO-CH 4 oxidation. Copyright © 2017. Published by Elsevier B.V.

  2. Variable Emissivity Electrochromics using Ionic Electrolytes and Low Solar Absorptance Coatings, Phase II

    Data.gov (United States)

    National Aeronautics and Space Administration — This work further developed a highly promising variable emissivity technology for spacecraft thermal control, based on unique conducting polymer (CP) electrochromics...

  3. Theoretical modeling of infrared emission from neutral and charged polycyclic aromatic hydrocarbons. II.

    NARCIS (Netherlands)

    Bakes, ELO; Tielens, AGGM; Bauschlicher, CW; Hudgins, DM; Allamandola, LJ

    2001-01-01

    The nature of the carriers of the interstellar infrared (IR) emission features between 3.3 and 12.7 mum is complex. We must consider emission from a family of polycyclic aromatic hydrocarbons (PAHs) in a multiplicity of cationic charge states (+1, +2, +3, and so on), along with neutral and anionic

  4. Air-assisted Liquid Liquid Microextraction Combined with Graphite Furnace Atomic Absorption Spectrometry for Preconcentration and Determination of Trace Amount of Co(II and Ni(II Ions in Water Samples

    Directory of Open Access Journals (Sweden)

    Saeed Mohammad Sorouraddin

    2017-12-01

    Full Text Available A simple, rapid and efficient method has been developed for the extraction, preconcentration and determination of cobalt (II and nickel (II ions in water samples by air-assisted liquid-liquid microextraction (AALLME coupled with graphite furnace atomic absorption spectrometry (GFAAS. In the proposed method, much less volume of an organic solvent was used as the extraction solvent in the absence of disperser solvent. Fine organic droplets were formed by sucking and injecting of the mixture of aqueous sample solution and extraction solvent with a syringe for several times in a conical test tube. After extraction, phase separation was performed by centrifugation and the enriched analytes in the sedimented phase were determined by GFAAS. Several variables that could affect the extraction efficiency were investigated and optimized. Calibration graphs were linear in the range of 6.5-100 ng L-1. Detection limits for Co and Ni were 2.3 ng L-1 and 3 ng L-1, respectively. The accuracy of the developed procedure was checked by analyzing NRCC-SLRS4 Riverine water as a certified reference material. Finally, the proposed method has been successfully applied for the determination of cobalt (II and nickel (II ions in tap, surface and river water samples.

  5. Estudio del equilibrio y cinética de adsorción de Cd(II, Ni(II y Cr(VI usando Quitosano y Quitosano modificado con cobre

    Directory of Open Access Journals (Sweden)

    M. Benavente

    2013-04-01

    Full Text Available En este trabajo, se estudió el equilibrio y la cinética de adsorción de Cd(II, Ni(II en quitosano y Cr(VI en quitosano modificado con cobre. Para ello, soluciones de iones metálicos a diferentes concentraciones, fueron puestas en contacto con el adsorbente y se agitaron por un período de 3 – 4 h. Al final del proceso, las muestras fueron analizadas en un espectrómetro de absorción atómica. Los datos experimentales del equilibrio de adsorción de los iones metálicos fueron evaluados aplicando las isotermas de Langmuir y Freundlich; mientras los datos cinéticos fueron evaluados utilizando los modelos cinéticos de pseudo-primer orden y pseudo-segundo orden. Los resultados del proceso demostraron que los iones fueron eficazmente adsorbidos por el quitosano (Cd y Ni y por el Cu-quitosano (Cr. Además, se comprobó que los datos experimentales del equilibrio de adsorción de Cr(VI y Ni(II se ajustan al modelo de Langmuir; mientras que los datos experimentales del Cd(II fueron mejor ajustados por el modelo de Freundlich. Mediante el uso de la isoterma de Langmuir se determinó la capacidad máxima de adsorción de cromo (29.7 mg/g Cu-quitosano, cadmio (102.0 mg/g quitosano y níquel (83.31 mg/g quitosano. Los resultados de la cinética de adsorción de los iones metálicos mostraron que los datos experimentales fueron mejor ajustados por el modelo de pseudo-segundo orden; es decir, el paso limitante en la velocidad es la reacción de adsorción y no la transferencia de masa.

  6. Flash Spectroscopy: Emission Lines From the Ionized Circumstellar Material Around 10-Day-Old Type II Supernovae

    Science.gov (United States)

    Khazov, D.; Yaron, O.; Gal-Yam, A.; Manulis, I.; Rubin, A.; Kulkarni, S. R.; Arcavi, I.; Kasliwal, M. M.; Ofek, E. O.; Cao, Y.; hide

    2016-01-01

    Supernovae (SNe) embedded in dense circumstellar material (CSM) may show prominent emission lines in their early-time spectra (spectroscopy"), we can measure various physical properties of the CSM, as well as the mass-loss rate of the progenitor during the year prior to its explosion. Searching through the Palomar Transient Factory (PTF and iPTF) SN spectroscopy databases from 2009 through 2014, we found 12 SNe II showing flash-ionized (FI) signatures in their first spectra. All are younger than 10 days. These events constitute 14% of all 84 SNe in our sample having a spectrum within 10 days from explosion, and 18% of SNe II observed at ages <5 days, thereby setting lower limits on the fraction of FI events. We classified as "blue/featureless" (BF) those events having a first spectrum that is similar to that of a blackbody, without any emission or absorption signatures. It is possible that some BF events had FI signatures at an earlier phase than observed, or that they lack dense CSM around the progenitor. Within 2 days after explosion, 8 out of 11 SNe in our sample are either BF events or show FI signatures. Interestingly, we found that 19 out of 21 SNe brighter than an absolute magnitude M(sub R) = -18.2 belong to the FI or BF groups, and that all FI events peaked above M(sub R) = -17.6 mag, significantly brighter than average SNe II.

  7. 40 CFR Table 4 to Subpart Bbbb of... - Model Rule-Class II Emission Limits for Existing Small Municipal Waste Combustion Unit a

    Science.gov (United States)

    2010-07-01

    ... Existing Small Municipal Waste Combustion Unit a 4 Table 4 to Subpart BBBB of Part 60 Protection of... NEW STATIONARY SOURCES Emission Guidelines and Compliance Times for Small Municipal Waste Combustion... Part 60—Model Rule—Class II Emission Limits for Existing Small Municipal Waste Combustion Unit a For...

  8. EPR spectroscopy of a family of Cr(III) 7M(II) (M = Cd, Zn, Mn, Ni) "wheels": studies of isostructural compounds with different spin ground states

    DEFF Research Database (Denmark)

    Piligkos, Stergios; Weihe, Høgni; Bill, Eckhard

    2009-01-01

    Spinning wheels: The presented highly resolved multifrequency continuous wave EPR spectra (e.g., see figure) of the heterooctametalic "wheels" Cr(7)M provide rare examples of high nuclearity polymetallic systems where detailed information on the spin-Hamiltonian parameters of the ground and excited...... spin states is observed.We present highly resolved multifrequency (X-, K-, Q- and W-band) continous wave EPR spectra of the heterooctametalic "wheels", [(CH(3))(2)NH(2)][Cr(III) (7)M(II)F(8)((CH(3))(3)CCOO)(16)], hereafter Cr(7)M, where M=Cd, Zn, Mn, and Ni. These experimental spectra provide rare...... to 10(5) by use of the Davidson algorithm. We show that transferability of spin-Hamiltonian parameters across complexes of the Cr(7)M family is possible and that the spin-Hamiltonian parameters of Cr(7)M do not have sharply defined values, but are rather distributed around a mean value....

  9. Greenhouse gas (CO2 and CH4) emissions from a high altitude hydroelectric reservoir in the tropics (Riogrande II, Colombia)

    Science.gov (United States)

    Guérin, Frédéric; Leon, Juan

    2015-04-01

    Tropical hydroelectric reservoirs are considered as very significant source of methane (CH4) and carbon dioxide (CO2), especially when flooding dense forest. We report emissions from the Rio Grande II Reservoir located at 2000 m.a.s.l. in the Colombian Andes. The dam was built at the confluence of the Rio Grande and Rio Chico in 1990. The reservoir has a surface of 12 km2, a maximum depth of 40m and a residence time of 2.5 month. Water quality (temperature, oxygen, pH, conductivity), nitrate, ammonium, dissolved and particulate organic carbon (DOC and POC), CO2 and CH4 were monitored bi-monthly during 1.5 year at 9 stations in the reservoir. Diffusive fluxes of CO2 and CH4 and CH4 ebullition were measured at 5 stations. The Rio grande II Reservoir is weakly stratified thermally with surface temperature ranging from 20 to 24°C and a constant bottom temperature of 18°C. The reservoir water column is well oxygenated at the surface and usually anoxic below 10m depth. At the stations close to the tributaries water inputs, the water column is well mixed and oxygenated from the surface to the bottom. As reported for other reservoirs located in "clear water" watersheds, the concentrations of nutrients are low (NO3-10 mmol m-2 d-1) were observed during the dry season. Close to the tributaries water inputs where the water column is well mixed, the average diffusive flux is 8 mmol m-2 d-1. CH4 ebullition was 3.5 mmol m-2 d-1 and no ebullition was observed for a water depth higher than 5m. The zone under the influence of the water inputs from tributaries represents 25% of the surface of the reservoir but contributed half of total CH4 emissions from the reservoir (29MgC month-1). Ebullition contributed only to 12% of total CH4 emissions over a year but it contributed up to 60% during the dry season. CH4 emissions from the Rio Grande Reservoir contributed 30% of the total GHG emissions (38GgCO2eq y-1). Overall, this study show that the majority of CH4 emissions from this

  10. Emission factors of air pollutants from CNG-gasoline bi-fuel vehicles: Part II. CO, HC and NOx.

    Science.gov (United States)

    Huang, Xiaoyan; Wang, Yang; Xing, Zhenyu; Du, Ke

    2016-09-15

    The estimation of emission factors (EFs) is the basis of accurate emission inventory. However, the EFs of air pollutants for motor vehicles vary under different operating conditions, which will cause uncertainty in developing emission inventory. Natural gas (NG), considered as a "cleaner" fuel than gasoline, is increasingly being used to reduce combustion emissions. However, information is scarce about how much emission reduction can be achieved by motor vehicles burning NG (NGVs) under real road driving conditions, which is necessary for evaluating the environmental benefits for NGVs. Here, online, in situ measurements of the emissions from nine bi-fuel vehicles were conducted under different operating conditions on the real road. A comparative study was performed for the EFs of black carbon (BC), carbon monoxide (CO), hydrocarbons (HCs) and nitrogen oxides (NOx) for each operating condition when the vehicles using gasoline and compressed NG (CNG) as fuel. BC EFs were reported in part I. The part II in this paper series reports the influence of operating conditions and fuel types on the EFs of CO, HC and NOx. Fuel-based EFs of CO showed good correlations with speed when burning CNG and gasoline. The correlation between fuel-based HC EFs and speed was relatively weak whether burning CNG or gasoline. The fuel-based NOx EFs moderately correlated with speed when burning CNG, but weakly correlated with gasoline. As for HC, the mileage-based EFs of gasoline vehicles are 2.39-12.59 times higher than those of CNG vehicles. The mileage-based NOx EFs of CNG vehicles are slightly higher than those of gasoline vehicles. These results would facilitate a detailed analysis of the environmental benefits for replacing gasoline with CNG in light duty vehicles. Copyright © 2016 Elsevier B.V. All rights reserved.

  11. Characterization and application of expanded graphite modified with phosphoric acid and glucose for the removal of Ni(II) from aqueous solution

    Science.gov (United States)

    Jiang, Li; Zhang, Jian; Xu, Xiaoli; Zhang, Jie; Liu, Hai; Guo, Zizhang; Kang, Yan; Li, Yiran; Xu, Jingtao

    2015-12-01

    Three kinds of modified expanded graphite (EG), impregnated with phosphoric acid (H3PO4) (P-EG), impregnated with glucose (G-EG), and impregnated with H3PO4 and glucose (G-P-EG), were prepared under a low temperature (150 °C). The adsorption capacity of G-P-EG (Qm = 7.016 mg/g) is much higher than original expanded graphite (EG Qm = 0.423 mg/g) and other two kinds of modified expanded graphite (P-EG Qm = 0.770 mg/g; G-EG Qm = 0.507 mg/g). The physicochemical properties of EG and G-P-EG were characterized by N2 adsorption/desorption, Boehm's titration and X-ray photoelectron spectroscopy (XPS). EG exhibited higher values of BET surface area (11.357 m2/g) and total pore volume (0.0303 cm3/g) than that of G-P-EG (4.808 m3/g and 0.0109 cm3/g). However, the results of Bohm's titration and XPS showed that G-P-EG contained more surface oxygen-containing functional groups. The Ni(II) adsorption equilibrium data agreed well with the Langmuir model. And the experimental data of EG and G-P-EG fitted better by pseudo-second order model. Based on the results of batch adsorption experiments and XPS analysis, there were several possible mechanisms for Ni(II) adsorption on the G-P-EG, including chemical adsorption, cation exchange, electrostatic attraction and surface complication.

  12. Electrophilic-Nucleophilic Dualism of Nickel(II) toward Ni···I Noncovalent Interactions: Semicoordination of Iodine Centers via Electron Belt and Halogen Bonding via σ-Hole.

    Science.gov (United States)

    Bikbaeva, Zarina M; Ivanov, Daniil M; Novikov, Alexander S; Ananyev, Ivan V; Bokach, Nadezhda A; Kukushkin, Vadim Yu

    2017-11-06

    The nitrosoguanidinate complex [Ni{NH═C(NMe 2 )NN(O)} 2 ] (1) was cocrystallized with I 2 and sym-trifluorotriiodobenzene (FIB) to give associates 1·2I 2 and 1·2FIB. Structures of these solid species were studied by XRD followed by topological analysis of the electron density distribution within the framework of Bader's approach (QTAIM) at the M06/DZP-DKH level of theory and Hirshfeld surface analysis. Our results along with inspection of XRD (CCDC) data, accompanied by the theoretical calculations, allowed the identification of three types of Ni···I contacts. The Ni···I semicoordination of the electrophilic nickel(II) center with electron belt of I 2 was observed in 1·2I 2 , the metal-involving halogen bonding between the nucleophilic nickel(II)-d z 2 center and σ-hole of iodine center was recognized and confirmed theoretically in the structure of [FeNi(CN) 4 (IPz)(H 2 O)] n (IPz = 4-N-coordinated 2-I-pyrazine), whereas the arrangement of FIB in 1·2FIB provides a boundary case between the semicoordination and the halogen Ni···I bondings. In 1·2I 2 and 1·2FIB, noncovalent interactions were studied by variable temperature XRD detecting the expansion of noncovalent contacts with preservation of covalent bond lengths upon the temperature increase from 100 to 300 K. The nature and energies of all identified types of the Ni···I noncovalent interactions in the obtained (1·2I 2 and 1·2FIB) and in the previously reported ([FeNi(CN) 4 (IPz)(H 2 O)] n , [NiL 2 ](I 3 ) 2 ·2I 2 (L = o-phenylene-bis(dimethylphosphine), [NiL]I 2 (L = 1,4,8,11-tetra-azacyclotetradecane), Ni(en) 2 ] n [AgI 2 ] 2n (en = ethylenediamine), and [NiL](ClO 4 ) (L = 4-iodo-2-((2-(2-(2-pyridyl)ethylsulfanyl)ethylimino)methyl)-phenolate)) structures were studied theoretically. The estimated strengths of these Ni···I noncovalent contacts vary from 1.6 to 4.1 kcal/mol and, as expected, become weaker on heating. This work is the first emphasizing electrophilic-nucleophilic dualism

  13. ISLSCP II Carbon Dioxide Emissions from Fossil Fuels, Cement, and Gas Flaring

    Data.gov (United States)

    National Aeronautics and Space Administration — ABSTRACT: This data set contains decadal (1950, 1960, 1970, 1980, 1990 and 1995) estimates of gridded fossil-fuel emissions, expressed in 1,000 metric tons C per...

  14. ISLSCP II Carbon Dioxide Emissions from Fossil Fuels, Cement, and Gas Flaring

    Data.gov (United States)

    National Aeronautics and Space Administration — This data set contains decadal (1950, 1960, 1970, 1980, 1990 and 1995) estimates of gridded fossil-fuel emissions, expressed in 1,000 metric tons C per year per one...

  15. ISLSCP II EDGAR 3 Gridded Greenhouse and Ozone Precursor Gas Emissions

    Data.gov (United States)

    National Aeronautics and Space Administration — ABSTRACT: The EDGAR (Emission Database for Global Atmospheric Research) database project is a comprehensive task carried out jointly by the National Institute for...

  16. Preliminary emissions assessment of conventional stationary combustion systems. Volume II. Final report, Mar--Dec 1975

    International Nuclear Information System (INIS)

    Surprenant, N.; Hall, R.; Slater, S.; Susa, T.; Sussman, M.

    1976-03-01

    The report gives results of a preliminary emissions assessment of the air, water, and solid waste pollutants produced by conventional stationary combustion systems. It gives results in four principal categories: utilities (electric generation), industrial (steam generation, space heating, and stationary engines), commercial/institutional (space heating and stationary engines), and residential (space heating). For each principal combustion system category, it gives: process types and operating efficiencies, fuel consumption, pollutant sources and characteristics, major research and development trends, fuel consumption trends, and technical areas where emission data are incomplete or unreliable. It also gives the pollutant emissions from applicable unit operations for each of 56 source classifications, using a uniform combustion source classification system. It identifies major gaps in available data regarding the population and capacity of combustion systems, application of control measures, fuel composition, and other parameters which significantly influence pollutant characteristics and emission rates

  17. ISLSCP II EDGAR 3 Gridded Greenhouse and Ozone Precursor Gas Emissions

    Data.gov (United States)

    National Aeronautics and Space Administration — The EDGAR (Emission Database for Global Atmospheric Research) database project is a comprehensive task carried out jointly by the National Institute for Public...

  18. Highly red-shifted NIR emission from a novel anthracene conjugated polymer backbone containing Pt( ii ) porphyrins

    KAUST Repository

    Freeman, D. M. E.

    2015-11-30

    © The Royal Society of Chemistry 2016. We present the synthesis of a novel diphenylanthracene (DPA) based semiconducting polymer. The polymer is solubilised by alkoxy groups attached directly to a DPA monomer, meaning the choice of co-monomer is not limited to exclusively highly solubilising moieties. Interestingly, the polymer shows a red-shifted elecroluminescence maximum (510 nm) when compared to its photoluminescence maximum (450 nm) which we attribute to excimer formation. The novel polymer was utilised as a host for a covalently-linked platinum(ii) complexed porphyrin dopant. Emission from these polymers was observed in the NIR and again showed almost a 100 nm red shift from photoluminescence to electroluminescence. This work demonstrates that utilising highly aggregating host materials is an effective tool for inducing red-shifted emission in OLEDs.

  19. Radio-frequency discharges in oxygen: II. Spatio-temporally resolved optical emission pattern

    Energy Technology Data Exchange (ETDEWEB)

    Dittmann, K; Drozdov, D; Krames, B; Meichsner, J [Institut fuer Physik, Universitaet Greifswald, D-17489 Greifswald (Germany)

    2007-11-07

    Axially and temporally resolved optical emission structures were investigated in the rf sheath region of a parallel plate capacitively coupled rf discharge (13.56 MHz) in pure oxygen and tetrafluoromethane. The rf discharge was driven at total pressures of between 10 and 100 Pa, gas flow rate of 3 sccm and rf power in the range 5-100 W. In particular, the emission of the atomic oxygen at 844.6 nm (3p{sup 3}P {yields} 3s{sup 3}S{sup 0}) and the atomic carbon at 193 nm (3s{sup 1}P{sup 0} {yields} 2p{sup 1}D) were imaged with a lens onto the entrance slit of a spectrometer and detected by a fast ICCD-camera. The spatio-temporally resolved analysis of the emission intensity during the rf cycle (73.75 ns) provides two significant excitation processes inside the rf sheath: the electron impact excitation at the sheath edge, and heavy particle impact excitation in front of the powered electrode. In oxygen plasma the emission of atomic oxygen was found in both regions whereas in tetrafluoromethane the emission of atomic carbon was observed only in front of the powered electrode. The experimental results reveal characteristic dependence of the emission pattern in front of the powered electrode on plasma process parameters (self-bias voltage, pressure) and allow an estimation of the excitation threshold energy and effective cross section of energetic heavy particle loss.

  20. Radio-frequency discharges in oxygen: II. Spatio-temporally resolved optical emission pattern

    Science.gov (United States)

    Dittmann, K.; Drozdov, D.; Krames, B.; Meichsner, J.

    2007-11-01

    Axially and temporally resolved optical emission structures were investigated in the rf sheath region of a parallel plate capacitively coupled rf discharge (13.56 MHz) in pure oxygen and tetrafluoromethane. The rf discharge was driven at total pressures of between 10 and 100 Pa, gas flow rate of 3 sccm and rf power in the range 5-100 W. In particular, the emission of the atomic oxygen at 844.6 nm (3p3P → 3s3S0) and the atomic carbon at 193 nm (3s1P0 → 2p1D) were imaged with a lens onto the entrance slit of a spectrometer and detected by a fast ICCD-camera. The spatio-temporally resolved analysis of the emission intensity during the rf cycle (73.75 ns) provides two significant excitation processes inside the rf sheath: the electron impact excitation at the sheath edge, and heavy particle impact excitation in front of the powered electrode. In oxygen plasma the emission of atomic oxygen was found in both regions whereas in tetrafluoromethane the emission of atomic carbon was observed only in front of the powered electrode. The experimental results reveal characteristic dependence of the emission pattern in front of the powered electrode on plasma process parameters (self-bias voltage, pressure) and allow an estimation of the excitation threshold energy and effective cross section of energetic heavy particle loss.

  1. Radio-frequency discharges in oxygen: II. Spatio-temporally resolved optical emission pattern

    International Nuclear Information System (INIS)

    Dittmann, K; Drozdov, D; Krames, B; Meichsner, J

    2007-01-01

    Axially and temporally resolved optical emission structures were investigated in the rf sheath region of a parallel plate capacitively coupled rf discharge (13.56 MHz) in pure oxygen and tetrafluoromethane. The rf discharge was driven at total pressures of between 10 and 100 Pa, gas flow rate of 3 sccm and rf power in the range 5-100 W. In particular, the emission of the atomic oxygen at 844.6 nm (3p 3 P → 3s 3 S 0 ) and the atomic carbon at 193 nm (3s 1 P 0 → 2p 1 D) were imaged with a lens onto the entrance slit of a spectrometer and detected by a fast ICCD-camera. The spatio-temporally resolved analysis of the emission intensity during the rf cycle (73.75 ns) provides two significant excitation processes inside the rf sheath: the electron impact excitation at the sheath edge, and heavy particle impact excitation in front of the powered electrode. In oxygen plasma the emission of atomic oxygen was found in both regions whereas in tetrafluoromethane the emission of atomic carbon was observed only in front of the powered electrode. The experimental results reveal characteristic dependence of the emission pattern in front of the powered electrode on plasma process parameters (self-bias voltage, pressure) and allow an estimation of the excitation threshold energy and effective cross section of energetic heavy particle loss

  2. Polycyclic Aromatic Hydrocarbon Emission in Spitzer /IRS Maps. II. A Direct Link between Band Profiles and the Radiation Field Strength

    Energy Technology Data Exchange (ETDEWEB)

    Stock, D. J.; Peeters, E., E-mail: dstock84@gmail.com [Department of Physics and Astronomy, University of Western Ontario, London, ON, N6A 3K7 (Canada)

    2017-03-10

    We decompose the observed 7.7 μ m polycyclic aromatic hydrocarbon (PAH) emission complexes in a large sample of over 7000 mid-infrared spectra of the interstellar medium using spectral cubes observed with the Spitzer /IRS-SL instrument. In order to fit the 7.7 μ m PAH emission complex we invoke four Gaussian components, which are found to be very stable in terms of their peak positions and widths across all of our spectra, and subsequently define a decomposition with fixed parameters, which gives an acceptable fit for all the spectra. We see a strong environmental dependence on the interrelationships between our band fluxes—in the H ii regions all four components are intercorrelated, while in the reflection nebulae (RNs) the inner and outer pairs of bands correlate in the same manner as previously seen for NGC 2023. We show that this effect arises because the maps of RNs are dominated by emission from strongly irradiated photodissociation regions, while the much larger maps of H ii regions are dominated by emission from regions much more distant from the exciting stars, leading to subtly different spectral behavior. Further investigation of this dichotomy reveals that the ratio of two of these components (centered at 7.6 and 7.8 μ m) is linearly related to the UV-field intensity (log G {sub 0}). We find that this relationship does not hold for sources consisting of circumstellar material, which are known to have variable 7.7 μ m spectral profiles.

  3. A new synthesis of enantiomerically pure syn-(S)-β-hydroxy-α-amino acids via asymmetric aldol reactions of aldehydes with a homochiral Ni(II)-glycine/(S)-BPB Schiff base complex

    NARCIS (Netherlands)

    Belokon, Yuri N.; Kochetkov, Konstantin A.; Ikonnikov, Nikolai S.; Strelkova, Tatiana V.; Harutyunyan, Syuzanna R.; Saghiyan, Ashot S.

    2001-01-01

    syn-(S)-β-Hydroxy-α-amino acids were synthesised stereoselectively via elaboration of the asymmetric aldol reactions of aldehydes with a chiral Ni(II)-(S)-BPB/glycine Schiff base complex in the presence of equimolar NaH in THF. The stereoselectivity of the reaction was studied as a function of time,

  4. Characterization of Ni(II) complexes of Schiff bases of amino acids and (S)-N-(2-benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide using ion trap and QqTOF electrospray ionization tandem mass spectrometry

    NARCIS (Netherlands)

    Jirasko, Robert; Holcapek, Michal; Kolarova, Lenka; Nadvornik, Milan; Popkov, Alexander

    This work demonstrates the application of electrospray ionization mass spectrometry (ESI-MS) using two different mass analyzers, ion trap and hybrid quadrupole time-of-flight (QqTOF) mass analyzer, for the structural characterization of Ni(II) complexes of Schiff bases of

  5. Emission solvatochromic behavior of a pentacoordinated Zn(II) complex: A viable tool for studying the metallodrug–protein interaction

    Energy Technology Data Exchange (ETDEWEB)

    Ricciardi, Loredana, E-mail: loredana.ricciardi@unical.it [Department of Chemistry and Chemical Technology, University of Calabria, I-87036 Rende (CS) (Italy); Centre of Excellence “Functional Nanostructured Materials” CEMIF.CAL, LASCAMM and CR INSTM, INSTM Calabria Unit, and CNR-IPCF-UOS Cosenza - Licryl Laboratory, I-87036 Rende (CS) (Italy); Pucci, Daniela; Pirillo, Sante; La Deda, Massimo [Department of Chemistry and Chemical Technology, University of Calabria, I-87036 Rende (CS) (Italy); Centre of Excellence “Functional Nanostructured Materials” CEMIF.CAL, LASCAMM and CR INSTM, INSTM Calabria Unit, and CNR-IPCF-UOS Cosenza - Licryl Laboratory, I-87036 Rende (CS) (Italy)

    2014-07-01

    A metal complex with antitumoral activity, Zn(Curcumin)(bypiridine)Cl, was characterized from a photophysical point of view, showing a green emission and a positive solvatochromism. These characteristics can be conveniently used to study its interaction with Human Serum Albumin (HSA), a protein carrier of many non-aqueous biologically-active compounds in the blood stream. The intrinsic fluorescence of HSA was quenched by Fluorescence Resonance Energy Transfer toward the Zn(II) complex, and the Stern–Volmer equation was applied to determine the bimolecular quenching rate constant of the interaction. - Highlights: • Albumin binding information is a key characteristic of drug pharmacology. • Fluorescence spectroscopy offers a simple method for revealing drug–protein interaction. • The fluorescence of the Zn(II) complex and its solvatochromisms has allowed studying the binding from a dual perspective.

  6. Syntheses, Characterization, and Antimicrobial Screening of N-(benzothiazol-2-ylbenzenesulphonamide and its Cu(I, Ni(II, Mn(II, Co(II, and Zn(II Complexes

    Directory of Open Access Journals (Sweden)

    N. L. Obasi

    2012-01-01

    Full Text Available N-(benzothiazol-2-ylbenzenesulphonamide (BS2ABT was synthesized by the condensation (by refluxing of 2-aminobenzothiazole and benzenesulphonylchloride in acetone at 140ºC. The resulting crude precipitates were recrystallized from dimethylformamide (DMF. Five metal complexes of copper(I, nickel(II, manganese(II, cobalt(II and zinc(II of the ligands were synthesized. The compounds were characterized using magnetic susceptibility measurements, UV/VIS spectrophotometry, infra red, proton and 13C nmr spectroscopies. The antimicrobial tests of the ligands and its metal complexes were carried out on both multi-resistant bacterial strains isolated under clinical conditions and cultured species using agar-well diffusion method. The multi-resistant bacterial strains used were Escherichia coli, Proteus species, Pseudomonas aeroginosa and Staphylococcus aureus which were isolated from dogs. The culture species were Pseudomonas aeruginosa (ATCC 27853, Escherichia Coli (ATCC 25922 Staphylococcus aureus (ATCC 25923, and the fungi, Candida krusei (ATCC 6258 and Candida albicans (ATCC 90028. The tests were both in vitro and in vivo. Thus the Inhibition Zone Diameter (IZD, the Minimum Inhibitory Concentration (MIC, and the Lethal and Effective Concentrations (LC50 and EC50 were determined. The antimicrobial activities of the compounds were compared with those of Ciprofloxacin and trimethoprim-sulphamethoxazole as antibacterial agents and Fluconazole as an antifungal drug. All the compounds showed varying activities against the cultured typed bacteria and fungi used. However, they were less active than the standard drugs used except Fluconazole which did not show any activity against Candida krusei (ATCC 6258 but most of the compounds synthesized were very active against it. The Lethal Concentration (LC50 ranged from 26.25±4.9-1833.88±186.92 ppm. These are within the permissible concentrations.

  7. Design, spectral characterization, thermal, DFT studies and anticancer cell line activities of Co(II), Ni(II) and Cu(II) complexes of Schiff bases derived from 4-amino-5-(pyridin-4-yl)-4H-1,2,4-triazole-3-thiol

    Science.gov (United States)

    Tyagi, Prateek; Chandra, Sulekh; Saraswat, B. S.; Yadav, Deepak

    2015-06-01

    A series of two biologically active Schiff base ligands L1, L2 have been synthesized in equimolar reaction of 4-amino-5-(pyridin-4-yl)-4H-1,2,4-triazole-3-thiol with thiophene-2-carbaldehyde and furan-2-carbaldehyde. The synthesized Schiff bases were used for complexation with different metal ions like Co(II), Ni(II) and Cu(II) by using a molar ratio of ligand: metal as 1:1 and 2:1. The characterization of Schiff bases and metal complexes was done by 1H NMR, UV-Vis, TGA, IR, mass spectrometry and molar conductivity studies. The in DFT studies the geometries of Schiff bases and metal complexes were fully optimized with respect to the energy using the 6-31+g(d,p) basis set. On the basis of the spectral studies an octahedral geometry has been assigned for Co(II), Ni(II) and Cu(II) complexes. The effect of these complexes on proliferation of human breast cancer cell line (MCF-7) and human hepatocellular liver carcinoma cell line (Hep-G2) were studied and compared with those of free ligand. The anticancer cell line results reveal that all metal complexes show moderate to significant % cytotoxicity on cell line HepG2 and MCF-7.

  8. New nano-complexes of Zn(II), Cu(II), Ni(II) and Co(II) ions; spectroscopy, thermal, structural analysis, DFT calculations and antimicrobial activity application

    Science.gov (United States)

    El-Shafiy, Hoda F.; Saif, M.; Mashaly, Mahmoud M.; Halim, Shimaa Abdel; Eid, Mohamed F.; Nabeel, A. I.; Fouad, R.

    2017-11-01

    This work presents synthesis, characterization, and application of several metal (II) complexes with (E)-2-hydroxy-N/-((thiophen-2-yl)methylene)benzohydrazide (H2L). Prepared complexes were identified by elemental, thermal, FT-IR, UV-Vis, 1H NMR, and XRD analysis, as well as molar conductivity and magnetic moment measurements. Changes in FT-IR and 1H NMR spectra of hydrazone ligand upon coordination indicated that the ligand behaves the same way as a monoanonic ligand with ONS donor sites. Kinetic parameters were determined for each thermal degradation stage of the ligand and its complexes using 'Coats-Redfern' method. All results confirm that all prepared compounds have 1:2 metal-to-ligand stoichiometry except Zn(II) complex, which has 1:1 metal-to-ligand stoichiometry. The antimicrobial activity for complexes was investigated. The antimicrobial activity results revealed that Zn(II) complex (1) has a good potency against gram positive bacteria (E. coli) and gram negative bacteria (P. vulgaris) in comparision with doxymycin standard, AT B3LYP/6-311G (d,p) level, Density Functional Theory (DFT) calculations were carried out to investigate the optimized structure of both, the ligand and the complexes. Total energy, energy of HOMO, and LUMO as well as Mullikan atomic charges were calculated. Dipole moment, orientation, and structure activity relationship were performed and discussed.DFT calculations, moreover, confirmed practical antimicrobial results.

  9. SOFIA-EXES Mid-IR Observations of [Fe II] Emission from the Extended Atmosphere of Betelgeuse

    Science.gov (United States)

    Harper, G. M.; DeWitt, C.; Richter, M. J.; Greathouse, T. K.; Ryde, N.; Guinan, E. F.; O'Gorman, E.; Vacca, W. D.

    2017-02-01

    We present a NASA-DLR SOFIA-Echelon Cross Echelle Spectrograph (EXES) and NASA Infrared Telescope Facility-Texas Echelon Cross Echelle Spectrograph (TEXES) mid-IR R≃ {{50,000}} spectral study of forbidden Fe II transitions in the early-type M supergiants, Betelgeuse (α Ori: M2 Iab) and Antares (α Sco: M1 Iab + B3 V). With EXES, we spectrally resolve the ground term [Fe II] 25.99 μm (a{}6{D}J=7/2{--9/2}: {E}{up}=540 K) emission from Betelgeuse. We find a small centroid blueshift of 1.9 ± 0.4 {km} {{{s}}}-1 that is a significant fraction (20%) of the current epoch wind speed, with a FWHM of 14.3 ± 0.1 {km} {{{s}}}-1. The TEXES observations of [Fe II] 17.94 μm (a{}4{F}J=7/2-9/2: {E}{up}={{3400}} K) show a broader FWHM of 19.1 ± 0.2 {km} {{{s}}}-1, consistent with previous observations, and a small redshift of 1.6 ± 0.6 {km} {{{s}}}-1 with respect to the adopted stellar center-of-mass velocity of {V}{CoM}=20.9+/- 0.3 {km} {{{s}}}-1. To produce [Fe II] 25.99 μm blueshifts of 20% wind speed requires that the emission arises closer to the star than existing thermal models for α Ori’s circumstellar envelope predict. This implies a more rapid wind cooling to below 500 K within 10{R}* ({θ }* =44 mas, dist = 200 pc) of the star, where the wind has also reached a significant fraction of the maximum wind speed. The line width is consistent with the turbulence in the outflow being close to the hydrogen sound speed. EXES observations of [Fe II] 22.90 μm (a{}4{D}J=5/2{--7/2}: {E}{up}={{11,700}} K) reveal no emission from either star. These findings confirm the dominance of cool plasma in the mixed region where hot chromospheric plasma emits copiously in the UV, and they also constrain the wind heating produced by the poorly understood mechanisms that drive stellar outflows from these low variability and weak-dust signature stars.

  10. SALT long-slit spectroscopy of quasar HE 0435-4312: fast displacement of the Mg II emission line

    Science.gov (United States)

    Średzińska, J.; Czerny, B.; Hryniewicz, K.; Krupa, M.; Kurcz, A.; Marziani, P.; Adhikari, T. P.; Basak, R.; You, B.; Wang, J.-M.; Hu, C.; Pych, W.; Bilicki, M.

    2017-05-01

    Context. The Mg II emission line is visible in the optical band for intermediate redshift quasars (0.4 frame. The Mg II line shape is clearly non-Gaussian but single-component, and the increase in line equivalent width and line shift is not accompanied with significant evolution of the line shape. We analyse the conditions in the Mg II and Fe II formation region and we note that the very large difference in the covering factor and the turbulent velocity also support the conclusion that the two regions are spatially separated. Conclusions: The measured acceleration of the line systematic shift is too large to connect it with the orbital motion at a distance of the BLR in this source. It may imply a precessing inner disk illuminating the BLR. Further monitoring is still needed to better constrain the variability mechanism. Based on observations made with the Southern African Large Telescope (SALT) under program 2012-2-POL-003 and 2013-1-POL-RSA-002 (PI: B. Czerny).Spectra shown in Figs. 3 and 4 are only available at the CDS via anonymous ftp to http://cdsarc.u-strasbg.fr (http://130.79.128.5) or via http://cdsarc.u-strasbg.fr/viz-bin/qcat?J/A+A/601/A32

  11. Synthesis and DNA binding studies of Ni(II), Co(II), Cu(II) and Zn(II) metal complexes of N 1,N 5-bis[pyridine-2-methylene]-thiocarbohydrazone Schiff-base ligand

    Science.gov (United States)

    Tiwari, A. D.; Mishra, A. K.; Mishra, S. B.; Mamba, B. B.; Maji, B.; Bhattacharya, S.

    2011-09-01

    The thiocarbohydrazone Schiff-base ligand with a nitrogen and sulphur donor was synthesized through condensation of pyridine-2-carbaldehyde and thiocarbohydrazide. Schiff-base ligands have the ability to conjugate with metal salts. A series of metal complexes with a general formula [MCl 2(H 2L)]· nH 2O (M dbnd Ni, Co, Cu and Zn) were synthesized by forming complexes of the N 1,N 5-bis[pyridine-2-methylene]-thiocarbohydrazone (H 2L) Schiff-base ligand. These metal complexes and ligand were characterized by using ultraviolet-visible (UV-Vis), Fourier Transform Infrared (FT-IR), 1H and 13C NMR spectroscopy and mass spectroscopy, physicochemical characterization, CHNS and conductivity. The biological activity of the synthesized ligand was investigated by using Escherichia coli DNA as target. The DNA interaction of the synthesized ligand and complexes on E. coli plasmid DNA was investigated in the aqueous medium by UV-Vis spectroscopy and the binding constant ( Kb) was calculated. The DNA binding studies showed that the metal complexes had an improved interaction due to trans-geometrical isomers of the complexes than ligand isomers in cis-positions.

  12. Technology Reinvestment Program/Advanced ``Zero Emission'' Control Valve (Phase II)

    Energy Technology Data Exchange (ETDEWEB)

    J. Napoleon

    1998-12-01

    The objectives of this effort are to determine, develop and demonstrate the feasibility of significantly reducing the cost and expanding the applications for a family of Advanced Zero Emissions Control Valves that meets the fugitive emissions requirements of the 1990 Amendments to the Clean Air Act. This program is a direct technology spin-off from the valve technology that is critical to the US Navy's Nuclear Powered Fleet. These zero emissions valves will allow the Hydrocarbon and Chemical Processing Industries, etc., to maintain their competitiveness and still meet environmental and safety requirements. Phase 2 is directed at refining the basic technologies developed during Phase 1 so that they can be more readily selected and utilized by the target market. In addition to various necessary certifications, the project will develop a full featured digital controller with ``smart valve'' growth capability, expanding valve sizes/applications and identifying valve materials to permit applications in severe operational environments.

  13. Luminous and variable stars in M31 and M33. II. Luminous blue variables, candidate LBVs, Fe II emission line stars, and other supergiants

    International Nuclear Information System (INIS)

    Humphreys, Roberta M.; Davidson, Kris; Weis, Kerstin; Bomans, D. J.; Burggraf, Birgitta

    2014-01-01

    An increasing number of non-terminal eruptions are being found in the numerous surveys for optical transients. Very little is known about these giant eruptions, their progenitors and their evolutionary state. A greatly improved census of the likely progenitor class, including the most luminous evolved stars, the luminous blue variables (LBVs), and the warm and cool hypergiants is now needed for a complete picture of the final pre-supernova stages of very massive stars. We have begun a survey of the evolved and unstable luminous star populations in several nearby resolved galaxies. In this second paper on M31 and M33, we review the spectral characteristics, spectral energy distributions, circumstellar ejecta, and evidence for mass loss for 82 luminous and variable stars. We show that many of these stars have warm circumstellar dust including several of the Fe II emission line stars, but conclude that the confirmed LBVs in M31 and M33 do not. The confirmed LBVs have relatively low wind speeds even in their hot, quiescent or visual minimum state compared to the B-type supergiants and Of/WN stars which they spectroscopically resemble. The nature of the Fe II emission line stars and their relation to the LBV state remains uncertain, but some have properties in common with the warm hypergiants and the sgB[e] stars. Several individual stars are discussed in detail. We identify three possible candidate LBVs and three additional post-red supergiant candidates. We suggest that M33-013406.63 (UIT301,B416) is not an LBV/S Dor variable, but is a very luminous late O-type supergiant and one of the most luminous stars or pair of stars in M33.

  14. Design, synthesis, characterization and antibacterial and antifungal activity of a new 2-{(E-[(4-aminophenylimino]-methyl}-4,6-dichlorophenol and its complexes with Co(II, Ni(II, Cu(II and Zn(II: An experimental and DFT study

    Directory of Open Access Journals (Sweden)

    Bakirdere Emine Gulhan

    2016-01-01

    Full Text Available In this study, the complexes of Co (II, Ni (II, Cu (II and Zn (II with 2-(E-(4-aminophenyliminomethyl-4,6-dichlorophenol were prepared and characterized by physical, spectral and analytical data. The metal: ligand stoichiometric ratio is 1:2 in all the complexes. The results suggested that the Schiff bases are coordinated to the metal ions through the phenolic oxygens and azomethine nitrogen to give mononuclear complexes. Their structures were elucidated on the basis of elemental analysis, IR, 1H and 13C NMR spectra, UV-VIS, magnetic susceptibility measurements and thermogravimetric analyses. Both the antibacterial and antifungal activities and MIC values of compounds were reported. Among the tested compounds, the most effective compound providing a MIC value of 64 μg/mL is Zn(L2 against C. tropicalis and B. subtilis. The theoretically optimized geometries of complexes have tetrahedral structures. The computed stretching frequencies of C=N, C-O and N-H bonds were found to be in good agreement with experimental data. All calculated frequencies fall within about 5% of the experimental frequency regions.

  15. CHARACTERIZATION OF MERCURY EMISSIONS AT A CHLOR-ALKALI PLANT, VOLUME II. APPENDICES F-J

    Science.gov (United States)

    The report gives results of a characterization of mercury (Hg) emissions at a chlor-alkali plant. Up to 160 short tons (146 Mg) of Hg is consumed by the chlor-alkali industry each year. Very little quantitative information is currently available however, on the actual Hg losses f...

  16. Evaluation of safety, performance and emissions of synthetic fuel blends in a Cessna Citation II

    NARCIS (Netherlands)

    Snijders, T.A.; Melkert, J.A.

    2011-01-01

    Prior to being used in aviation, alternative fuels have to be tested thoroughly to ensure safe operation. At Delft University of Technology, a test programme was performed to evaluate the safety, performance and emissions of synthetic fuel blends. During test preparations, compatibility of the

  17. Ingresos hospitalarios en el niño: Caracterización en un área de salud (II

    Directory of Open Access Journals (Sweden)

    Freddie Hernández Cisneros

    1999-01-01

    Full Text Available Se realizó un estudio transversal con 150 niños egresados del Hospital Pediátrico Docente de Camagüey y procedentes del Policlínico Comunitario Docente Centro de dicha ciudad, durante el año 1998 y con el fin de realizarles una caracterización. A cada uno de ellos se le aplicó una encuesta con variables tales como: conocimiento de su Médico de la Familia del ingreso, atención por él antes, si habia sido remitido o no, las interconsultas previas, visitas hospitalarias efectuadas, calidad de las anotaciones en las historias clínicas, interrelación con los médicos de la atención secundaria y valoración al egreso; procesándose los datos obtenidos en una microcomputadora IBM compatible e ilustrándose los resultados en forma de tablas. Se encontraron como resultados más importantes: en un 11,30 % de los pacientes su médico desconocía el ingreso; el 36,60 % no fue valorado nunca antes del ingreso por él, ni se remitió el 16,60 %; hecho significativo fue que el 72,60 % no fue interconsultado con el Profesor de Pediatría del Grupo Básico de Trabajo, así mismo, el 32 % no fue visitado nunca en el hospital por ningún integrante del binomio médico-enfermera, no detectándose dificultades en las anotaciones de las historias clínicas ni en la interrelación con los médicos de la atención hospitalaria de los visitados, cumpliéndose adecuadamente la valoración después del egreso por el Médico de la Familia.A cross-sectional study was conducted with 150 children from the Central Tesching Community Polyclinic of Camagüey that were discharged from the Pediatric Teaching Hospital of that city during 1998 in order to characterize them. A survey was done taking into account the following variables: whether the family physician knaw about the admission, attention received before being admitted in hospital, whether the patient had been referred, previous interconsultations, visits to the hospital, quality of the annotations made in

  18. SHARC-II 350 μm Observations of Thermal Emission from Warm Dust in z >= 5 Quasars

    Science.gov (United States)

    Wang, Ran; Wagg, Jeff; Carilli, Chris L.; Benford, Dominic J.; Dowell, C. Darren; Bertoldi, Frank; Walter, Fabian; Menten, Karl M.; Omont, Alain; Cox, Pierre; Strauss, Michael A.; Fan, Xiaohui; Jiang, Linhua

    2008-04-01

    We present observations of four z >= 5 SDSS quasars at 350 μm with the SHARC-II bolometer camera on the Caltech Submillimeter Observatory. These are among the deepest observations that have been made by SHARC-II at 350 μm, and three quasars are detected at >=3σ significance, greatly increasing the sample of 350 μm (corresponds to rest frame wavelengths of = 5), detected high-redshift quasars. The derived rest frame far-infrared (FIR) emission in the three detected sources is about five to ten times stronger than that expected from the average spectral energy distribution (SED) of the local quasars given the same 1450 Å luminosity. Combining the previous submillimeter and millimeter observations at longer wavelengths, the temperatures of the FIR-emitting warm dust from the three quasar detections are estimated to be in the range of 39-52 K. Additionally, the FIR-to-radio SEDs of the three 350 μm detections are consistent with the emission from typical star-forming galaxies. The FIR luminosities are ~1013 L sun and the dust masses are >=108 M sun. These results confirm that huge amounts of warm dust can exist in the host galaxies of optically bright quasars as early as z ~ 6. The universe is so young at these epochs (~1 Gyr) that a rapid dust-formation mechanism is required. We estimate the size of the FIR dust-emission region to be about a few kpc, and further provide a comparison of the SEDs among different kinds of dust-emitting sources to investigate the dominant dust-heating mechanism.

  19. Magnetic properties of the weak itinerant-electron ferromagnet Ni75Al25: II. The effect of compositional disorder

    Science.gov (United States)

    Kaul, S. N.; Semwal, Anita

    2004-12-01

    The results of a detailed study of the magnetic properties of well-characterized polycrystalline NipAl100-p (73.5~{\\mathrm {at.{\\%}}} \\le p \\le 76~{\\mathrm {at.{\\%}}} ) alloys are presented and discussed in the light of the existing theories. Extreme care has been exercised in the sample preparation to ensure that the site disorder (invariably present in any alloy system) does not interfere with the compositional disorder brought about by the reduction in the concentration of the magnetic (Ni) atoms. Thus, the observed variation in the magnetic properties with Ni concentration (p) is solely controlled by the compositional disorder. Like site disorder, compositional disorder smears out the sharp features in the density of states (DOS) curve near the Fermi level, EF, and reduces the DOS at EF, N(EF), and thereby causes a fall (an enhancement) in the values (value) of the spontaneous magnetization at 0 K, M0, the spin-wave stiffness at 0 K, D0, and the Curie temperature, TC (zero-field differential susceptibility at 0 K, χ0). However, compositional disorder, unlike site disorder, gives rise to smooth variations in N(EF), the inverse Stoner enhancement factor {\\cal S}^{-1}=I N(E_{\\mathrm {F}})-1 , M0, D0, TC, D0/TC and χ0 with p. These variations in the case of M0(p), D0(p) and TC(p) are very well described by the power laws M_{0}(p) \\sim (p-p_{\\mathrm {c}})^{\\beta _{\\mathrm {p}}} , D_{0}(p) \\sim (p-p_{\\mathrm {c}})^{\\theta_{\\mathrm {p}}} and T_{\\mathrm {C}}(p) \\sim (p-p_{\\mathrm {c}})^{\\phi } with p>pc (pc = the percolation threshold for the appearance of long-range ferromagnetic order) predicted by the percolation theories for these quantities on a regular three-dimensional (d = 3) percolating network. The alloys in question exhibit a crossover in the spin dynamics from the hydrodynamic (magnon) to critical (fracton) regime at a well-defined temperature Tco*(p). An elaborate analysis of the magnetization data in terms of the percolation models

  20. Selective solid phase extraction of copper using a new Cu(II)-imprinted polymer and determination by inductively coupled plasma optical emission spectroscopy (ICP-OES)

    OpenAIRE

    Yilmaz, Vedat; Arslan, Zikri; Hazer, Orhan; Yilmaz, Hayriye

    2013-01-01

    This work reports the preparation of a novel Cu(II)-ion imprinted polymer using 2-thiozylmethacrylamide (TMA) for on-line preconcentration of Cu(II) prior to its determination by inductively coupled optical emission spectroscopy (ICP-OES). Cu(II)-TMA monomer (complex) was synthesized and copolymerized via bulk polymerization method in the presence of ethyleneglycoldimethacrylate cross-linker. The resulting polymer was washed with 5% (v/v) HNO3 to remove Cu(II) ions and then with water until a...

  1. 40 CFR Appendix II to Part 1068 - Emission-Related Parameters and Specifications

    Science.gov (United States)

    2010-07-01

    ... dimension. 4. Camshaft timing. a. Valve opening—intake exhaust (degrees from top-dead center or bottom-dead center). b. Valve closing—intake exhaust (degrees from top-dead center or bottom-dead center). c. Valve... bottom-dead center). II. Intake Air System. 1. Roots blower/supercharger/turbocharger calibration. 2...

  2. A Parameter Study for Modeling Mg ii h and k Emission during Solar Flares

    Energy Technology Data Exchange (ETDEWEB)

    Rubio da Costa, Fatima [Department of Physics, Stanford University, Stanford, CA 94305 (United States); Kleint, Lucia, E-mail: frubio@stanford.edu [University of Applied Sciences and Arts Northwestern Switzerland, 5210, Windisch (Switzerland)

    2017-06-20

    Solar flares show highly unusual spectra in which the thermodynamic conditions of the solar atmosphere are encoded. Current models are unable to fully reproduce the spectroscopic flare observations, especially the single-peaked spectral profiles of the Mg ii h and k lines. We aim to understand the formation of the chromospheric and optically thick Mg ii h and k lines in flares through radiative transfer calculations. We take a flare atmosphere obtained from a simulation with the radiative hydrodynamic code RADYN as input for a radiative transfer modeling with the RH code. By iteratively changing this model atmosphere and varying thermodynamic parameters such as temperature, electron density, and velocity, we study their effects on the emergent intensity spectra. We reproduce the typical single-peaked Mg ii h and k flare spectral shape and approximate the intensity ratios to the subordinate Mg ii lines by increasing either densities, temperatures, or velocities at the line core formation height range. Additionally, by combining unresolved upflows and downflows up to ∼250 km s{sup −1} within one resolution element, we reproduce the widely broadened line wings. While we cannot unambiguously determine which mechanism dominates in flares, future modeling efforts should investigate unresolved components, additional heat dissipation, larger velocities, and higher densities and combine the analysis of multiple spectral lines.

  3. Polarization anisotropy of the emission from type-II quantum dots

    Czech Academy of Sciences Publication Activity Database

    Klenovský, P.; Hemzal, D.; Steindl, P.; Zíková, Markéta; Křápek, V.; Humlíček, J.

    2015-01-01

    Roč. 92, č. 24 (2015), 1-5, č. článku 241302. ISSN 1098-0121 Institutional support: RVO:68378271 Keywords : quantum dot * type II heterostructure * polarization anisotropy * III-V semiconductors Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 3.736, year: 2014

  4. Inter-comparison between HERMESv2.0 and TNO-MACC-II emission data using the CALIOPE air quality system (Spain)

    Science.gov (United States)

    Guevara, Marc; Pay, María Teresa; Martínez, Francesc; Soret, Albert; Denier van der Gon, Hugo; Baldasano, José M.

    2014-12-01

    This work examines and compares the performance of two emission datasets on modelling air quality concentrations for Spain: (i) the High-Elective Resolution Modelling Emissions System (HERMESv2.0) and (ii) the TNO-MACC-II emission inventory. For this purpose, the air quality system CALIOPE-AQFS (WRF-ARW/CMAQ/BSC-DREAM8b) was run over Spain for February and June 2009 using the two emission datasets (4 km × 4 km and 1 h). Nitrogen dioxide (NO2), sulphur dioxide (SO2), Ozone (O3) and particular matter (PM10) modelled concentrations were compared with measurements at different type of air quality stations (i.e. rural background, urban, suburban industrial). A preliminary emission comparison showed significant discrepancies between the two datasets, highlighting an overestimation of industrial emissions in urban areas when using TNO-MACC-II. However, simulations showed similar performances of both emission datasets in terms of air quality. Modelled NO2 concentrations were similar between both datasets at the background stations, although TNO-MACC-II presented lower underestimations due to differences in industrial, other mobile sources and residential emissions. At Madrid urban stations NO2 was significantly underestimated in both cases despite the fact that HERMESv2.0 estimates traffic emissions using a more local information and detailed methodology. This NO2 underestimation problem was not found in Barcelona due to the influence of international shipping emissions located in the coastline. An inadequate characterization of some TNO-MACC-II's point sources led to high SO2 biases at industrial stations, especially in northwest Spain where large facilities are grouped. In general, surface O3 was overestimated regardless of the emission dataset used, depicting the problematic of CMAQ on overestimating low ozone at night. On the other hand, modelled PM10 concentrations were less underestimated in urban areas when applying HERMESv2.0 due to the inclusion of road dust

  5. ACEMAN (II): a PDP-11 software package for acoustic emission analysis

    International Nuclear Information System (INIS)

    Tobias, A.

    1976-01-01

    A powerful, but easy-to-use, software package (ACEMAN) for acoustic emission analysis has been developed at Berkeley Nuclear Laboratories. The system is based on a PDP-11 minicomputer with 24 K of memory, an RK05 DISK Drive and a Tektronix 4010 Graphics terminal. The operation of the system is described in detail in terms of the functions performed in response to the various command mnemonics. The ACEMAN software package offers many useful facilities not found on other acoustic emission monitoring systems. Its main features, many of which are unique, are summarised. The ACEMAN system automatically handles arrays of up to 12 sensors in real-time operation during which data are acquired, analysed, stored on the computer disk for future analysis and displayed on the terminal if required. (author)

  6. Detection of multiple AE signal by triaxial hodogram analysis; Sanjiku hodogram ho ni yoru taju acoustic emission no kenshutsu

    Energy Technology Data Exchange (ETDEWEB)

    Nagano, K.; Yamashita, T. [Muroran Institute of Technology, Hokkaido (Japan)

    1997-05-27

    In order to evaluate dynamic behavior of underground cracks, analysis and detection were attempted on multiple acoustic emission (AE) events. The multiple AE is a phenomenon in which multiple AE signals generated by underground cracks developed in an extremely short time interval are superimposed, and observed as one AE event. The multiple AE signal consists of two AE signals, whereas the second P-wave is supposed to have been inputted before the first S-wave is inputted. The first P-wave is inputted first, where linear three-dimensional particle movements are observed, but the movements are made random due to scattering and sensor characteristics. When the second P-wave is inputted, the linear particle movements are observed again, but are superimposed with the existing input signals and become multiple AE, which creates poor S/N ratio. The multiple AE detection determines it a multiple AE event when three conditions are met, i. e. a condition of equivalent time interval of a maximum value in a scalogram analysis, a condition of P-wave vibrating direction, and a condition of the linear particle movement. Seventy AE signals observed in the Kakkonda geothermal field were analyzed and AE signals that satisfy the multiple AE were detected. However, further development is required on an analysis method with high resolution for the time. 4 refs., 4 figs.

  7. Superradiant and stimulated-superradiant emission in prebunched electron-beam radiators. II. Radiation enhancement schemes

    Directory of Open Access Journals (Sweden)

    A. Gover

    2005-03-01

    Full Text Available Further enhancement of the intense coherent superradiant and stimulated-superradiant emission from prebunched electron beams is possible, in schemes of prebunched beam radiation devices, and particularly free electron laser (FEL. The enhancement of coherent power and spectral power by use of a waveguide, particularly at the zero-slippage condition, is evaluated. A special scheme of a stimulated-superradiance FEL oscillator is analyzed and is shown to feature ultimate radiative energy conversion efficiency (near 100%.

  8. Evolving Starburst Modeling of FIR/sub-mm/mm Line Emission. II. Application to M 82

    OpenAIRE

    Yao, Lihong

    2009-01-01

    We present starburst models for far-infrared/sub-millimeter/millimeter (FIR/sub-mm/mm) line emission of molecular and atomic gas in an evolving starburst region, which is treated as an ensemble of non-interacting hot bubbles which drive spherical shells of swept-up gas into a surrounding uniform gas medium. These bubbles and shells are driven by stellar winds and supernovae within massive star clusters formed during an instantaneous starburst. The underlying stellar radiation from the evolvin...

  9. Hydrothermal synthesis of wurtzite Zn{sub 1−x}Ni{sub x}S mesoporous nanospheres: With blue–green emissions and ferromagnetic Curie point above room temperature

    Energy Technology Data Exchange (ETDEWEB)

    Amaranatha Reddy, D.; Kim, D.H.; Rhee, S.J.; Jung, C.U.; Lee, B.W.; Liu, Chunli, E-mail: chunliliu@hufs.ac.kr

    2014-03-05

    Highlights: • Wurtzite Zn{sub 1−x}Ni{sub x}S mesoporous nanospheres were synthesized via hydrothermal method. • Structural, band gap, PL and magnetization studies were carried out. • All the doped samples exhibited intrinsic room temperature ferromagnetism. • The maximum PL enhancement was noticed in 2 at.% Ni doped ZnS nanospheres. • Zn{sub 1−x}Ni{sub x}S nanospheres may find applications in luminescent and spintronic devices. -- Abstract: Wurtzite Zn{sub 1−x}Ni{sub x}S (x = 0.00, 0.01, 0.02, 0.03, 0.04 and 0.05) mesoporous nanospheres were successfully synthesized via a versatile hydrothermal method with the assistance of ethylenediamine (EN). The as synthesized nanospheres were uniform, mono-dispersed with a spherical shape. Microstructure investigations revealed that these nanospheres were mesoporous clusters of Zn{sub 1−x}Ni{sub x}S nanoparticles with the size around 5 nm. X-ray Diffraction, X-ray photoelectron spectroscopy, and Energy-dispersive X-ray spectroscopy studies confirmed that the Ni ions substituted into ZnS host lattice without altering the crystal structure. The Fourier-transform infrared spectra confirmed the coupling between the EN molecules and ZnS. The absorption edge in the diffuse reflection spectra shifted towards lower wavelength with increasing Ni concentration, indicating an expansion in the band gap energy that is estimated to be in the range of 3.53–3.60 eV. The photoluminescence spectra of the doped and un-doped samples contained a broad emission band covering the range of 350–650 nm. Room temperature magnetization studies indicated that the undoped ZnS nanospheres yielded only diamagnetism, whereas the doped samples exhibited ferromagnetism that can be attributed to the Ni{sup 2+} dopants. The temperature dependence of magnetization revealed that the Zn{sub 1−x}Ni{sub x}S nanospheres have Curie point above room temperature. The intrinsic ferromagnetism and ferromagnetic Curie point above room temperature

  10. Characterization and application of expanded graphite modified with phosphoric acid and glucose for the removal of Ni(II) from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, Li [Shandong Key Laboratory of Water Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Zhang, Jian, E-mail: zhangjian00@sdu.edu.cn [Shandong Key Laboratory of Water Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Xu, Xiaoli [Shandong Key Laboratory of Water Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Zhang, Jie [Shandong Experimental High School, Jinan 250100 (China); Liu, Hai; Guo, Zizhang; Kang, Yan; Li, Yiran [Shandong Key Laboratory of Water Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Xu, Jingtao [School of Municipal and Environmental Engineering, Shandong Jianzhu University, Jinan 250100 (China)

    2015-12-01

    Highlights: • Glucose and H{sub 3}PO{sub 4}, single or together, were used to modify expanded graphite. • The modified condition was at a low temperature (150 °C). • The properties of EG and the highest adsorption ability modified EG were compared. • G-P-EG has the highest adsorption ability, which is much higher than that of EG. - Abstract: Three kinds of modified expanded graphite (EG), impregnated with phosphoric acid (H{sub 3}PO{sub 4}) (P-EG), impregnated with glucose (G-EG), and impregnated with H{sub 3}PO{sub 4} and glucose (G-P-EG), were prepared under a low temperature (150 °C). The adsorption capacity of G-P-EG (Q{sub m} = 7.016 mg/g) is much higher than original expanded graphite (EG Q{sub m} = 0.423 mg/g) and other two kinds of modified expanded graphite (P-EG Q{sub m} = 0.770 mg/g; G-EG Q{sub m} = 0.507 mg/g). The physicochemical properties of EG and G-P-EG were characterized by N{sub 2} adsorption/desorption, Boehm's titration and X-ray photoelectron spectroscopy (XPS). EG exhibited higher values of BET surface area (11.357 m{sup 2}/g) and total pore volume (0.0303 cm{sup 3}/g) than that of G-P-EG (4.808 m{sup 3}/g and 0.0109 cm{sup 3}/g). However, the results of Bohm's titration and XPS showed that G-P-EG contained more surface oxygen-containing functional groups. The Ni(II) adsorption equilibrium data agreed well with the Langmuir model. And the experimental data of EG and G-P-EG fitted better by pseudo-second order model. Based on the results of batch adsorption experiments and XPS analysis, there were several possible mechanisms for Ni(II) adsorption on the G-P-EG, including chemical adsorption, cation exchange, electrostatic attraction and surface complication.

  11. Characterization and application of expanded graphite modified with phosphoric acid and glucose for the removal of Ni(II) from aqueous solution

    International Nuclear Information System (INIS)

    Jiang, Li; Zhang, Jian; Xu, Xiaoli; Zhang, Jie; Liu, Hai; Guo, Zizhang; Kang, Yan; Li, Yiran; Xu, Jingtao

    2015-01-01

    Highlights: • Glucose and H 3 PO 4 , single or together, were used to modify expanded graphite. • The modified condition was at a low temperature (150 °C). • The properties of EG and the highest adsorption ability modified EG were compared. • G-P-EG has the highest adsorption ability, which is much higher than that of EG. - Abstract: Three kinds of modified expanded graphite (EG), impregnated with phosphoric acid (H 3 PO 4 ) (P-EG), impregnated with glucose (G-EG), and impregnated with H 3 PO 4 and glucose (G-P-EG), were prepared under a low temperature (150 °C). The adsorption capacity of G-P-EG (Q m = 7.016 mg/g) is much higher than original expanded graphite (EG Q m = 0.423 mg/g) and other two kinds of modified expanded graphite (P-EG Q m = 0.770 mg/g; G-EG Q m = 0.507 mg/g). The physicochemical properties of EG and G-P-EG were characterized by N 2 adsorption/desorption, Boehm's titration and X-ray photoelectron spectroscopy (XPS). EG exhibited higher values of BET surface area (11.357 m 2 /g) and total pore volume (0.0303 cm 3 /g) than that of G-P-EG (4.808 m 3 /g and 0.0109 cm 3 /g). However, the results of Bohm's titration and XPS showed that G-P-EG contained more surface oxygen-containing functional groups. The Ni(II) adsorption equilibrium data agreed well with the Langmuir model. And the experimental data of EG and G-P-EG fitted better by pseudo-second order model. Based on the results of batch adsorption experiments and XPS analysis, there were several possible mechanisms for Ni(II) adsorption on the G-P-EG, including chemical adsorption, cation exchange, electrostatic attraction and surface complication.

  12. NURE aerial gamma-ray and magnetic reconnaissance survey, Colorado-Arizona area: Salton Sea NI II-9, Phoenix NI 12-7, El Centro NI II-12, AJO NI 12-10, Lukeville NH 12-1 quadrangles. Volume I. Narrative report

    International Nuclear Information System (INIS)

    1979-11-01

    A rotary-wing reconnaissance high sensitivity radiometric and magnetic survey, encompassing several 1:250,000 quadrangles in southwestern Arizona and southeastern California, was performed. The surveyed area consisted of approximately 9300 line miles. The radiometric data were corrected and normalized to 400 feet terrain clearance. The data were identified as to rock type by correlating the data samples with existing geologic maps. Statistics defining the mean and standard deviation of each rock type are presented as listings in Volume I of this report. The departure of the data from its corresponding mean rock type is computed in terms of standard deviation units and is presented graphically as anomaly maps in Volume II and as computer listings in microfiche form in Volume I. Profiles of the normalized averaged data are contained in Volume II and include traces of the potassium, uranium and thorium count rates, corresponding ratios, and several ancilliary sensor data traces, magnetometer, radio altimeter and barometric pressure height. A description of the local geology is provided, and a discussion of the magnetic and radiometric data is presented together with an evaluation of selected uranium anomalies

  13. Burning of wood slabs in a conical calorimeter. Part II: emissions, oxygen consumed and exhaust temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Costa, Fernando de Souza; Castro, Andre de [Instituto Nacional de Pesquisas Espaciais (INPE), Cachoeira Paulista, SP (Brazil). Lab. Associado de Combustao e Propulsao], e-mail: fernando@lcp.inpe.br, e-mail: andre@lcp.inpe.br

    2006-07-01

    This work presents experimental data concerning the combustion characteristics of wood slabs of pinus (Pinus elliot) burned in a conical calorimeter. Emissions of CO, Co2, No and UHC, oxygen molar fractions and temperatures of exhaust gases from burning slabs (10 X 10 X 5 cm 3) were measured. The combustion behaviour during pre-heating, drying, self-ignition, pyrolysis, flaming and smoldering, for a constant cone calorimeter output of 2000 W, is compared and analysed for slabs with heated surfaces parallel and perpendicular to the wood fibers(author)

  14. Herschel Spectroscopy of the Taffy Galaxies (UGC 12914/12915 = VV 254): Enhanced [C II] Emission in the Collisionally Formed Bridge

    Science.gov (United States)

    Peterson, B. W.; Appleton, P. N.; Bitsakis, T.; Guillard, P.; Alatalo, K.; Boulanger, F.; Cluver, M.; Duc, P.-A.; Falgarone, E.; Gallagher, S.; Gao, Y.; Helou, G.; Jarrett, T. H.; Joshi, B.; Lisenfeld, U.; Lu, N.; Ogle, P.; Pineau des Forêts, G.; van der Werf, P.; Xu, C. K.

    2018-03-01

    Using the PACS and SPIRE spectrometers on board Herschel, we obtained observations of the Taffy galaxies (UGC 12914/12915) and bridge. The Taffy system is believed to be the result of a face-on collision between two gas-rich galaxies, in which the stellar disks passed through each other, but the gas was dispersed into a massive H I and molecular bridge between them. Emission is detected and mapped in both galaxies and the bridge in the [C II]157.7 μm and [O I]63.2 μm fine-structure lines. Additionally, SPIRE FTS spectroscopy detects the [C I] {}3{{{P}}}2\\to {}3{{{P}}}1(809.3 {GHz}) and [C I] {}3{{{P}}}1\\to 3{{{P}}}0(492.2 {GHz}) neutral carbon lines, and weakly detects high-J CO transitions in the bridge. These results indicate that the bridge is composed of a warm multi-phase medium consistent with shock and turbulent heating. Despite low star formation rates in the bridge, the [C II] emission appears to be enhanced, reaching [C II]/FIR ratios of 3.3% in parts of the bridge. Both the [C II] and [O I] lines show broad intrinsic multi-component profiles, similar to those seen in previous CO (1–0) and H I observations. The [C II] emission shares similar line profiles with both the double-peaked H I profiles and shares a high-velocity component with single-peaked CO profiles in the bridge, suggesting that the [C II] emission originates in both the neutral and molecular phases. We show that it is feasible that a combination of turbulently heated H2 and high column-density H I, resulting from the galaxy collision, is responsible for the enhanced [C II] emission.

  15. Facile, one-pot and scalable synthesis of highly emissive aqueous-based Ag,Ni:ZnCdS/ZnS core/shell quantum dots with high chemical and optical stability

    Science.gov (United States)

    Sahraei, Reza; Soheyli, Ehsan; Faraji, Zahra; Soleiman-Beigi, Mohammad

    2017-11-01

    We report here on a one-pot, mild and low cost aqueous-based synthetic route for the preparation of colloidally stable and highly luminescent dual-doped Ag,Ni:ZnCdS/ZnS core/shell quantum dots (QDs). The pure dopant emission of the Ni-doped core/shell QDs was found to be highly affected by the presence of a second dopant ion (Ag+). Results showed that the PL emission intensity increases while its peak position experiences an obvious blue shift with an increase in the content of Ag+ ions. Regarding the optical observations, we provide a simple scheme for absorption-recombination processes of the carriers through impurity centers. To obtain optimum conditions with a better emission characteristic, we also study the effect of different reaction parameters, such as refluxing temperature, the pH of the core and shell solution, molar ratio of the dopant ions (Ni:(Zn+Cd) and Ag:(Zn+Cd)), and concentration of the core and shell precursors. Nonetheless, the most effective parameter is the presence of the ZnS shell in a suitable amount to eliminate surface trap states and enhance their emission intensity. It can also improve the bio-compatibility of the prepared QDs by restricting the Cd2+ toxic ions inside the core of the QDs. The present suggested route also revealed the remarkable optical and chemical stability of the colloidal QDs which establishes them as a decent kind of nano-scale structure for light emitting applications, especially in biological technologies. The suggested process also has the potential to be scaled-up while maintaining the emission characteristics and structural quality necessary for industrial applications in optoelectronic devices.

  16. Facile, one-pot and scalable synthesis of highly emissive aqueous-based Ag,Ni:ZnCdS/ZnS core/shell quantum dots with high chemical and optical stability.

    Science.gov (United States)

    Sahraei, Reza; Soheyli, Ehsan; Faraji, Zahra; Soleiman-Beigi, Mohammad

    2017-11-24

    We report here on a one-pot, mild and low cost aqueous-based synthetic route for the preparation of colloidally stable and highly luminescent dual-doped Ag,Ni:ZnCdS/ZnS core/shell quantum dots (QDs). The pure dopant emission of the Ni-doped core/shell QDs was found to be highly affected by the presence of a second dopant ion (Ag + ). Results showed that the PL emission intensity increases while its peak position experiences an obvious blue shift with an increase in the content of Ag + ions. Regarding the optical observations, we provide a simple scheme for absorption-recombination processes of the carriers through impurity centers. To obtain optimum conditions with a better emission characteristic, we also study the effect of different reaction parameters, such as refluxing temperature, the pH of the core and shell solution, molar ratio of the dopant ions (Ni:(Zn+Cd) and Ag:(Zn+Cd)), and concentration of the core and shell precursors. Nonetheless, the most effective parameter is the presence of the ZnS shell in a suitable amount to eliminate surface trap states and enhance their emission intensity. It can also improve the bio-compatibility of the prepared QDs by restricting the Cd 2+ toxic ions inside the core of the QDs. The present suggested route also revealed the remarkable optical and chemical stability of the colloidal QDs which establishes them as a decent kind of nano-scale structure for light emitting applications, especially in biological technologies. The suggested process also has the potential to be scaled-up while maintaining the emission characteristics and structural quality necessary for industrial applications in optoelectronic devices.

  17. Tunable colors and white-light emission based on a microporous luminescent Zn(II)-MOF.

    Science.gov (United States)

    He, Hongming; Sun, Fuxing; Borjigin, Tsolmon; Zhao, Nian; Zhu, Guangshan

    2014-03-07

    Metal-organic frameworks (MOFs) are a rapidly growing class of hybrid materials with many multifunctional properties. The permanent porosity plays a central role in the functional properties. In particular, the luminescent MOFs with a permanent porosity have wide applications in guest species recognition and adsorption. In this contribution, we aim to develop tunable colors and white-light luminescence materials by the encapsulation of Ln(3+) species in microporous luminescent MOFs. A semi-rigid trivalent carboxylic acid 1,3,5-tri(4-carboxyphenoxy)benzene (H3TCPB) was selected as the organic building block, not only because it is suitable to construct microporous frameworks, but also by reason of its blue luminescent emission. Under solvothermal reactions, a microporous MOF material, [Zn3(TCPB)2(H2O)2]·2H2O·4DMF (JUC-113, JUC = Jilin University, China), was synthesized, which has a permanent porosity and emits blue light. According to three-primary colors, the guest luminescent species should be Tb(3+) and Eu(3+) owing to their distinctive colors (Tb(3+), green; Eu(3+), red). In addition, the luminescent properties of JUC-113 can be easily tuned by different combinations of the encapsulation amount of Tb(3+) and Eu(3+), obtaining white-light emission materials.

  18. Emission, Dispersion, Transformation, and Deposition of Asian Particulates Over the Western Pacific Ocean. Part II

    International Nuclear Information System (INIS)

    Turco, Richard P.

    2005-01-01

    In this project we developed and applied a coupled three-dimensional meteorology/chemistry/microphysics model to study the patterns of aerosol dispersion and deposition in the western Pacific area; carried out a series of detailed regional aerosol simulations to test the ability of models to treat emission, dispersion and removal processes prior to long-range transport; calculated and analyzed trajectories that originate in Asian dust source regions and reach the Pacific Basin; performed detailed simulations of regional and trans-Pacific transport, as well as the microphysical and chemical properties, of aerosols in the Asia-Pacific region to quantify processes that control the emission, dispersion and removal of particles; and assessed the contributions of regional-scale Asian particulate sources to the deposition of pollutants onto surface waters. The transport and deposition of aerosols and vapors were found to be strongly controlled by large and synoptic scale meteorology, convection, turbulence, and precipitation, as well as strong interactions between surface conditions and topographical features. The present analysis suggests that accurate representations of aerosol sources, transport and deposition can be obtained using a comprehensive modeling approach

  19. Synthesis of non-toxic As and Cr nanoparticles through redox activity of highly flexible layered coordination polymer of Ni(II)

    Science.gov (United States)

    Agarwal, Rashmi A.

    2018-03-01

    A simple method for the sequestration of As(III) and Cr(VI) from water has been demonstrated by utilizing a highly flexible porous coordination polymer (PCP) of Ni(II) in its as synthesized form or without solvent removal. This PCP reduces the high toxicity of As(III) and Cr(VI) ions into non-toxic As(0) and Cr/Cr2O3/CrO2 (zero, tri and tetravalent) nanoparticles (NPs) within its pores, and this is characterized by powder x-ray diffraction, x-ray photoelectron spectroscopy and high-resolution transmission electron microscopy analysis. The high functionality of this polymer is due to the presence of monodentate carboxylate groups of a benzenetricarboxylate linker, which provide anchoring sites to the metal ions of the metal precursors. Due to the highly oxidising nature of these toxic ions, a redox reaction takes place between the framework metal ions and toxic metal ions, which is explained by an electron paramagnetic resonance study. This is the first report to synthesize non-toxic, as well as useful, NPs of As and Cr from their highly toxic ions within the cavities of a PCP for remediation of the toxic waste stream and contaminated waste water.

  20. p-halo N4-phenyl substituted thiosemicarbazones: Crystal structure, supramolecular architecture, characterization and bio-assay of their Co(III) and Ni(II) complexes

    Science.gov (United States)

    Kotian, Avinash; Kumara, Karthik; Kamat, Vinayak; Naik, Krishna; Kokare, Dhoolesh G.; Nevrekar, Anupama; Lokanath, Neratur Krishnappagowda; Revankar, Vidyanand K.

    2018-03-01

    In the present work, three potential metal ion chelating ligands, p-halo N4-phenyl substituted thiosemicarbazones are synthesized and characterized. The molecular structure of all (E)-4-(4-halophenyl)-1-(3-hydroxyiminobutan-2-ylidene) thiosemicarbazones (halo = F/Cl/Br) are determined by single crystal X-ray diffraction method. All the molecules have crystallized in monoclinic crystal system with P21/n space group. The ligands show Csbnd H⋯S and Nsbnd H⋯S intermolecular interactions, which are responsible to form the supramolecular self-assemblies through R22(8), R22(12) and R22(14) ring motifs. Hirshfeld surface analysis is carried out to explore the intermolecular interactions. A series of Co(III) and Ni(II) mononuclear transition metal complexes derived from these ligands have been synthesized and characterized by various spectro-analytical methods. The metal to ligand stoichiometry has been found to be 1:2 in all the complexes. The synthesized compounds have been investigated for their in vitro antimicrobial potencies. The compounds are found to be more active than the standard used, in the case of E. coli and A. niger. Additionally, they are also screened for their in vitro antitubercular activity.

  1. Simultaneous removal of Ni(II and fluoride from a real flue gas desulfurization wastewater by electrocoagulation using Fe/C/Al electrode

    Directory of Open Access Journals (Sweden)

    Shinian Liu

    2017-09-01

    Full Text Available Large amounts of anions and heavy metals coexist in flue gas desulfurization (FGD wastewater originating from coal-fired power plants, which cause serious environmental pollution. Electrocoagulation (EC with Fe/C/Al hybrid electrodes was investigated for the separation of fluoride and nickel ions from a FGD wastewater. The study mainly focused on the technology parameters including anode electrode type, time, inter-electrode distance (5–40 mm, current density (1.88–6.25 mA/cm2 and initial pH (4–10. The results showed that favorable nickel and fluoride removal were obtained by increasing the time and current density, but this led to an increase in energy consumption. Eighty-six percent of fluoride and 98% of Ni(II were removed by conducting the Fe/C/Al EC with a current density of 5.00 mA/cm2 and inter-electrode distance of 5 mm at pH 4 for 25 min and energy consumption was 1.33 kWh/m3. Concomitant pollutants also achieved excellent treatment efficiency. The Hg, Mn, Pb, Cd, Cu, SS and chemical oxygen demand were reduced by 90%, 89%, 92%, 88%, 98%, 99.9% and 89%, respectively, which met stringent environmental regulations.

  2. 2-D Laser-Calibrated Doppler Images of HeII and CIII Emission on DIII-D

    Science.gov (United States)

    Allen, S. L.; Samuell, Cameron; Meyer, W. H.

    2017-10-01

    Recent improvements to the DIII-D CIS system have reduced the error bars of the inferred Doppler velocity by over an order of magnitude, i.e. to 0.1 km/s. Coherence imaging of plasma emission superimposes an interferogram on the plasma image, and the interferometer phase is a sensitive measure of the central wavelength of the emission. A tuneable diode laser calibration image at 465 nm is automatically acquired between plasma shots and provides the rest wavelength in the lab frame; the wavelength is measured with a wavemeter to 0.01 pm. The interferometer is stabilized mechanically and thermally with a unique system so that the interferometer drift between calibrations is small. These improvements have enabled tomographically inverted images of main ion He II parallel flow in the divertor during He plasma operation. The parallel flow, as expected, is observed to depend on the direction of the B × ∇B drift, which is reversed by changing the direction of the toroidal field. For many conditions, the C III Doppler velocity is also in the same direction as the main ion. Work supported by the US DOE under DE-FC02-04ER54698 and DE-AC52-07NA27344. LLNL-ABS-88688.

  3. Molecule formation and infrared emission in fast interstellar shocks. II. Dissociation speeds for interstellar shock waves

    International Nuclear Information System (INIS)

    Hollenbach, D.; McKee, C.F.

    1980-01-01

    The postshock destruction of molecules is examined, including the processes of (i) collisions with neutral hydrogen atoms and molecules, (ii) electronic collisions, and (iii) neutral chemical reactions with atoms, particularly atomic hydrogen. Using conservative estimates of collisional dissociation rates from individual vibrational states, we find that process (i) leads to the destruction of molecular hydrogen behind shocks with speeds v/sub s/> or approx. =25 km s -1 if the preshock molecular gas has hydrogen nucleus densities of n 0 > or approx. =10 4 cm -3 . At lower densities (n 0 approx. =10 2 cm -3 ), destruction occurs for v/sub s/> or approx. =50 km s -1 and process (ii) dominates. Dissociation of molecules such as CO, H 2 O, and O 2 follows the destruction of H 2 , as the resultant hydrogen atoms chemically dissociate the metal atoms from their bonds (process iii) in the hot postshock gas. These results demonstrate that many of the observed high-speed interstellar molecules, if shock accelerated, must have dissociated and reformed in the postshock gas

  4. Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases. Part 2: aldol, Mannich addition reactions, deracemization and (S) to (R) interconversion of α-amino acids.

    Science.gov (United States)

    Sorochinsky, Alexander E; Aceña, José Luis; Moriwaki, Hiroki; Sato, Tatsunori; Soloshonok, Vadim

    2013-11-01

    This review provides a comprehensive treatment of literature data dealing with asymmetric synthesis of α-amino-β-hydroxy and α,β-diamino acids via homologation of chiral Ni(II) complexes of glycine Schiff bases using aldol and Mannich-type reactions. These reactions proceed with synthetically useful chemical yields and thermodynamically controlled stereoselectivity and allow direct introduction of two stereogenic centers in a single operation with predictable stereochemical outcome. Furthermore, new application of Ni(II) complexes of α-amino acids Schiff bases for deracemization of racemic α-amino acids and (S) to (R) interconversion providing additional synthetic opportunities for preparation of enantiomerically pure α-amino acids, is also reviewed. Origin of observed diastereo-/enantioselectivity in the aldol, Mannich-type and deracemization reactions, generality and limitations of these methodologies are critically discussed.

  5. UNDERSTANDING THE AGN-HOST CONNECTION IN BROAD Mg II EMISSION-SELECTED AGN-HOST HYBRID QUASARS

    International Nuclear Information System (INIS)

    Wang, J.; Wei, J. Y.

    2009-01-01

    We study the issue of active galactic nucleus (AGN)-host connection in intermediate-z (1.2>z > 0.4) galaxies with hybrid spectra (hybrid QSOs for short). The observed spectra redward of the Balmer limit are dominated by starlight, and the spectra at the blue end by both an AGN continuum and an Mg II broad emission line. This unique property allows us to examine both an AGN and its host galaxy in an individual galaxy simultaneously. First, 15 hybrid QSOs are selected from the Sloan Digital Sky Survey (SDSS) Data Release 6. The spectra are then analyzed in detail for three objects: SDSS J162446.49+461946.7, SDSS J102633.32+103443.8, and SDSS J090036.44+381353.0. Our spectral analysis shows that the current star formation activities are strongly suppressed, and that the latest burst ages range from ∼400 Myr to 1 Gyr. Based on the Mg II black hole masses, the three hybrid QSOs are consistent with the D n (4000) - L/L Edd sequence that was previously established in local AGNs. The three hybrid QSOs are located in the middle range of the sequence, which implies that the hybrid QSOs are at the transition stage not only from young to old AGNs, but also from a host-dominated phase to an AGN-dominated phase.

  6. Competition between dynamical and statistical particle emissions in 3618Ar + 5828Ni reactions. Search for a critical phenomenon signal in central collisions of 12954Xe + nat50Sn

    International Nuclear Information System (INIS)

    Buchet, Philippe

    1999-01-01

    Nuclear reactions at the Fermi energy range provide a mean of studying nuclei interaction mechanisms, energy dissipation process and deexcitation phenomena. Heavy ion collisions offer an additional window to on the 'nuclear liquid' phase diagram, in particular its 'critical zone'. We study all these points by analysing the 36 18 Ar + 58 28 Ni and the 129 54 Xe + nat 50 Sn reactions, measured with the 4π INDRA detector. We study light particles production properties from 32 MeV/u to 95 MeV/u. Inclusive measurements show that increasing the incident energies leads to a linear increase of the maximum number of Z = 1 and Z = 2 particles, whereas that of Z ≥ 3 increases weakly. The transverse energy of the Z = 1 and Z = 2 corresponds to a constant fraction of the available energy, whereas this of Z ≥ 3 decreases between 30 MeV/u and 50 MeV/u, and then converges. The same trends appear in the 129 54 Xe + nat 50 Sn reactions, between 25 MeV/u and 50 MeV/u. The incident energy is mostly goes into producing more and more light particles. In addition, a more precise study of the reactions, selecting them according to the charge of the detected quasi-projectile residue (QPR). Whatever the incident energy is, the charge of the QPR is associated to the same mean impact parameter, and the production cross sections of QPR of a given charge also superimpose. These observations suggest a geometrical production mechanism of the QP. The transverse mean energy at a fixed parallel velocity reveals another emission source (MR) at an intermediate velocity between the remnants of the projectile (QP) and of the target (QT). The fit of two thermal surface emission (QP and QT) and one thermal volume emission (MR) on dσ/dν z and (E-perpendicular)(ν z ) establishes that the temperature of the QP depends essentially on the impact parameter, not on the incident energy, whereas the apparent temperature of MR increases strongly with the available energy. The MR source

  7. EVOLVING STARBURST MODELING OF FAR-INFRARED/SUBMILLIMETER/MILLIMETER LINE EMISSION. II. APPLICATION TO M 82

    International Nuclear Information System (INIS)

    Yao Lihong

    2009-01-01

    We present starburst models for far-infrared/sub-millimeter/millimeter line emission of molecular and atomic gas in an evolving starburst region, which is treated as an ensemble of noninteracting hot bubbles that drive spherical shells of swept-up gas into a surrounding uniform gas medium. These bubbles and shells are driven by stellar winds and supernovae within massive star clusters formed during an instantaneous starburst. The underlying stellar radiation from the evolving clusters affects the properties and structure of photodissociation regions (PDRs) in the shells, and hence the spectral energy distributions (SEDs) of the molecular and atomic line emission from these swept-up shells and the associated parent giant molecular clouds contain a signature of the stage of evolution of the starburst. The physical and chemical properties of the shells and their structure are computed using a simple, well-known similarity solution for the shell expansion, a stellar population synthesis code, and a time-dependent PDR chemistry model. The SEDs for several molecular and atomic lines ( 12 CO and its isotope 13 CO, HCN, HCO + , C, O, and C + ) are computed using a nonlocal thermodynamic equilibrium line radiative transfer model. By comparing our models with the available observed data of nearby infrared bright galaxies, especially M 82, we constrain the models and in the case of M 82, we provide estimates for the ages (5-6 Myr, 10 Myr) of recent starburst activity. We also derive a total H 2 gas mass of ∼(2-3.4) x 10 8 M sun for the observed regions of the central 1 kpc starburst disk of M 82.

  8. Synthesis and stereochemical assignments of diastereomeric Ni(II) complexes of glycine Schiff base with (R)-2-(N-{2-[N-alkyl-N-(1-phenylethyl)amino]acetyl}amino)benzophenone; a case of configurationally stable stereogenic nitrogen.

    Science.gov (United States)

    Moriwaki, Hiroki; Resch, Daniel; Li, Hengguang; Ojima, Iwao; Takeda, Ryosuke; Aceña, José Luis; Soloshonok, Vadim A

    2014-01-01

    A family of chiral ligands derived from α-phenylethylamine and 2-aminobenzophenone were prepared by alkylation of the nitrogen atom. Upon reaction with glycine and a Ni(II) salt, these ligands were transformed into diastereomeric complexes, as a result of the configurational stability of the stereogenic nitrogen atom. Different diastereomeric ratios were observed depending on the substituent R introduced in the starting ligand, and stereochemical assignments were based on X-ray analysis, along with NMR studies and optical rotation measurements.

  9. Fuzzy logic modeling of Pb (II) sorption onto mesoporous NiO/ZnCl2-Rosa Canina-L seeds activated carbon nanocomposite prepared by ultrasound-assisted co-precipitation technique.

    Science.gov (United States)

    Javadian, Hamedreza; Ghasemi, Maryam; Ruiz, Montserrat; Sastre, Ana Maria; Asl, Seyed Mostafa Hosseini; Masomi, Mojtaba

    2018-01-01

    In this study, NiO/Rosa Canina-L seeds activated carbon nanocomposite (NiO/ACNC) was prepared by adding dropwise NaOH solution (2mol/L) to raise the suspension pH to around 9 at room temperature under ultrasonic irradiation (200W) as an efficient method and characterized by FE-SEM, FTIR and N 2 adsorption-desorption isotherm. The effect of different parameters such as contact time (0-120min), initial metal ion concentration (25-200mg/L), temperature (298, 318 and 333K), amount of adsorbent (0.002-0.007g) and the solution's initial pH (1-7) on the adsorption of Pb (II) was investigated in batch-scale experiments. The equilibrium data were well fitted by Langmuir model type 1 (R 2 >0.99). The maximum monolayer adsorption capacity (q m ) of NiO/ACNC was 1428.57mg/L. Thermodynamic parameters (ΔG°, ΔH° and ΔS°) were also calculated. The results showed that the adsorption of Pb (II) onto NiO/ACNC was feasible, spontaneous and exothermic under studied conditions. In addition, a fuzzy-logic-based model including multiple inputs and one output was developed to predict the removal efficiency of Pb (II) from aqueous solution. Four input variables including pH, contact time (min), dosage (g) and initial concentration of Pb (II) were fuzzified using an artificial intelligence-based approach. The fuzzy subsets consisted of triangular membership functions with eight levels and a total of 26 rules in the IF-THEN approach which was implemented on a Mamdani-type of fuzzy inference system. Fuzzy data exhibited small deviation with satisfactory coefficient of determination (R 2 >0.98) that clearly proved very good performance of fuzzy-logic-based model in prediction of removal efficiency of Pb (II). It was confirmed that NiO/ACNC had a great potential as a novel adsorbent to remove Pb (II) from aqueous solution. Copyright © 2017 Elsevier B.V. All rights reserved.

  10. Mononuclear Ni(II) complexes of Schiff base ligands formed from unsymmetrical tripodal amines of differing arm lengths: Spectral, X-ray crystal structural, antimicrobial and DNA cleavage activity

    Science.gov (United States)

    Keypour, Hassan; Shayesteh, Maryam; Rezaeivala, Majid; Dhers, Sébastien; Küp, Fatma Öztürk; Güllü, Mithat; Ng, Seikweng

    2017-11-01

    The synthesis of two unsymmetrical N-capped tripodal amines, 2-((4-aminobutyl)(pyridin-2-ylmethyl)amino)ethanol (3) and 3-((2-aminoethyl)(pyridin-2-ylmethyl)amino)propan-1-ol (4) is reported. They feature a longer, 3-hydroxypropyl or butylamino arm than that in the analogues previously employed. All four tripodal amines, 1-4, are equipped with a 2-methylpyridyl-arm, and either an ethylamino-arm (1 and 4), propylamino-arm (2) or butylamino-arm (3). The amines, 3 and 4, have been employed in one pot condensation reactions with salicylaldehyde and its derivatives in the presence of Ni(II) metal ion. A series of new mononuclear complexes, [NiIILaldi](ClO4) or [NiIILaldi(solvent)](ClO4) with different geometry, of Schiff base ligands were generated. X-ray crystal structure determinations of [NiIILOMe3(H2O)](ClO4)·2H2O and [NiIILOMe4](ClO4) revealed them to be mononuclear. The Ni(II) ion in [NiIILOMe4](ClO4) complex is in a distorted square-planar environment whilst this ion is in distorted octahedral environment in [NiIILOMe3(H2O)](ClO4)·2H2O complex despite the longer arm length of L3. While, in related systems in our previous work, they had led to dimeric complexes. These results clearly showed that the variation of the arm lengths of the ligands and metal ions has a remarkable impact on the formation and structure of the complexes. The cleavage of DNA by all synthesised complexes was examined using gel electrophoresis experiments. Also, the antibacterial effects of components were determined against the three Gram-positive bacteria, and against the three Gram-negative bacteria and against the three yeast Candida albicans ATCC 10231, Candida krusei ATCC 1424 and Candida tropicalis ATCC 13803.

  11. Ultraviolet high-excitation Fe II fluorescence lines excited by O VI, C IV, and H I resonance emission as seen in IUE spectra

    International Nuclear Information System (INIS)

    Feibelman, W.A.; Bruhweiler, F.C.; Johansson, S.

    1991-01-01

    Archival high-dispersion spectra from the IUE are used in a search for Bowen emission lines of Fe II excited by the stronger transition of the O VI resonance doublet. The possibility of using these Fe II emission lines as a diagnostic of the strength of the far-ultraviolet emission of O VI at 1032 A is explored. It is found that the Fe II emission lines are quite common and strong in symbiotic stars, particularly those of the type known as 'symbiotic novae', as well as in normal novae. The lines are observed in central stars of some planetary nebulae of the O VI sequence besides a few central stars of type WR. High density, high excitation, and high temperature are suggested to be requirements for the excitation of the Fe II fluorescence lines. It is pointed out that while these lines were observed in PG 1159-035 and K1-16, they were not observed in AGNs. 22 refs

  12. Omitting radiotherapy in early positron emission tomography-negative stage I/II Hodgkin lymphoma is associated with an increased risk of early relapse

    DEFF Research Database (Denmark)

    Raemaekers, John M M; André, Marc P E; Federico, Massimo

    2014-01-01

    PURPOSE: Combined-modality treatment is standard treatment for patients with clinical stage I/II Hodgkin lymphoma (HL). We hypothesized that an early positron emission tomography (PET) scan could be used to adapt treatment. Therefore, we started the randomized EORTC/LYSA/FIL Intergroup H10 trial ...

  13. Central stars of planetary nebulae. II. New OB-type and emission-line stars

    Science.gov (United States)

    Weidmann, W. A.; Gamen, R.

    2011-07-01

    Context. There are more than 3000 confirmed and probably known Galactic planetary nebulae (PNe), but central star spectroscopic information is available for only 13% of them. Aims: We have undertaken a spectroscopic survey of the central stars in PNe to identify their spectral types. Methods: We performed spectroscopic observations at low resolution with the 2-m telescope at CASLEO, Argentina. Results: We present the spectra of 46 central stars of PNe, most of them are OB-type and emission-line stars. Based on data collected at the Complejo Astronómico El Leoncito (CASLEO), which is operated under agreement between the Consejo Nacional de Investigaciones Científicas y Técnicas de la República Argentina y Universidades Nacionales de La Plata, Córdoba y San Juan, Argentina.The reduced spectra (FITS files) are available in electronic form at the CDS via anonymous ftp to cdsarc.u-strasbg.fr (130.79.128.5) or via http://cdsarc.u-strasbg.fr/viz-bin/qcat?J/A+A/531/A172

  14. Photoelectron spectroscopy study on Li substituted NiO using PES beamline installed on Indus-1

    CERN Document Server

    Banerjee, A; Phase, D M; Dasannacharya, B A

    2003-01-01

    Photoelectron spectroscopy beamline based on a toroidal grating monochromator (TGM) is recently commissioned on Indus-1 storage ring. It has been used to carry out valence band photoemission study of Li substituted NiO. In this paper initially a brief description of the beamline components and the experimental station for angle integrated photoemission experiment is presented. The later part of this paper is devoted to studies carried out on Li sub x Ni sub 1 sub - sub x O with x=0.0, 0.35 and 0.5 samples. Thin pellets of polycrystalline samples were used for the measurements reported here. Valence band spectra recorded on polycrystalline Li sub x Ni sub 1 sub - sub x O samples show drastic changes in various features as compared to that of pure NiO. The prominent changes are: (i) change in the relative contributions of Ni-3d and O-2p emissions, (ii) change in the peak position of Ni-3d from the top of the valance band of NiO and (iii) no noticeable change in the Ni satellite peak. These results are evaluated...

  15. Evaluation of adsorption capacities of humic acids extracted from Algerian soil on polyaniline for application to remove pollutants such as Cd(II), Zn(II) and Ni(II) and characterization with cavity microelectrode.

    Science.gov (United States)

    Terbouche, Achour; Ramdane-Terbouche, Chafia Ait; Hauchard, Didier; Djebbar, Safia

    2011-01-01

    The adsorption capacities of new humic acids isolated from Yakouren forest (YHA) and Sahara (Tamenrasset: THA) soils (Algeria) and commercial humic acid (PFHA) on polyaniline emeraldine base (PEB) were studied at pH 6.6. Also the adsorption of heavy metals such as Cd2+, Zn2+ and Ni2+ on humic acid-polyaniline systems (HA-PEB) was investigated at the same conditions. HA-PEB compounds were characterized by scanning electron microscopy (SEM), infrared spectrometry and cavity microelectrode. In addition, batch adsorption and cavity microelectrode were used in the adsorption study of Cd2+, Zn2+ and Ni2+ on HA-PEB. To develop biocaptors of polluting metals using a cavity microelectrode modified by HA-PEB systems, the adsorption kinetic and adsorption capacity were investigated. The SEM analysis showed that the presence of humic acid affected the PEB surface and caused the formation of a granular morphology. The maximum adsorption capacities (q(max)) of PFHA, THA and YHA determined by adsorption isotherms were 91.31, 132.1 and 151.0 mg/g, respectively. Batch adsorption results showed that q(max) of Cd2+, Zn2+ and Ni2+ on HA-PEB followed the order: THA-PEB > YHA-PEB > PFHA-PEB. The voltammograms obtained with HA-PEB modified cavity microelectrode showed the appearance of new redox couples reflecting the adsorption of HA on PEB. Metal-humic acid-polyaniline voltammograms were characterized by appearance of oxidation-reduction couples or reduction wave corresponding to metal. Finally, the result may be exploited to develop a biocaptor based on the cavity microelectrode amended by THA-PEB and YHA-PEB.

  16. Three-dimensional modeling of diesel engine intake flow, combustion and emissions-II

    Energy Technology Data Exchange (ETDEWEB)

    Reitz, R.D.; Rutland, C.J.

    1993-09-01

    A three-dimensional computer code, KIVA, is being modified to include state-of-the-art submodels for diesel engine flow and combustion. Improved and/or new submodels which have already been implemented and previously reported are: Wall heat transfer with unsteadiness and compressibility, laminar-turbulent characteristic time combustion with unburned HC and Zeldo`vich NO{sub x}, and spray/wall impingement with rebounding and sliding drops. Progress on the implementation of improved spray drop drag and drop breakup models, the formulation and testing of a multistep kinetics ignition model and preliminary soot modeling results are described in this report. In addition, the use of a block structured version of KIVA to model the intake flow process is described. A grid generation scheme has been developed for modeling realistic (complex) engine geometries, and computations have been made of intake flow in the ports and combustion chamber of a two-intake-valve engine. The research also involves the use of the code to assess the effects of subprocesses on diesel engine performance. The accuracy of the predictions is being tested by comparisons with engine experiments. To date, comparisons have been made with measured engine cylinder pressure, temperature and heat flux data, and the model results are in good agreement with the experiments. Work is in progress that will allow validation of in-cylinder flow and soot formation predictions. An engine test facility is described that is being used to provide the needed validation data. Test results have been obtained showing the effect of injection rate and split injections on engine performance and emissions.

  17. Selective dispersive liquid-liquid microextraction and preconcentration of Ni(II) into a micro droplet followed by ETAAS determination using a yellow Schiff's base bisazanyl derivative

    Energy Technology Data Exchange (ETDEWEB)

    Alizadeh, Kamal, E-mail: Alizadehk@yahoo.com [Department of Chemistry, Lorestan University, Khorramabad (Iran, Islamic Republic of); Nemati, Hadi; Zohrevand, Somaieh; Hashemi, Payman; Kakanejadifard, Ali [Department of Chemistry, Lorestan University, Khorramabad (Iran, Islamic Republic of); Shamsipur, Mojtaba [Department of Chemistry, Razi University, Kermanshah (Iran, Islamic Republic of); Ganjali, Mohammad Reza [Center of Excellence in Electrochemistry, University of Tehran, Tehran (Iran, Islamic Republic of); Endocrinology and Metabolism Research Center, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Faridbod, Farnoush [Endocrinology and Metabolism Research Center, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of)

    2013-03-01

    A simple, rapid and sensitive method was developed for the selective separation and preconcentration of Ni(II) using dispersive liquid-liquid microextraction, by a yellow Schiff's base bisazanyl derivative, as a selective complexing agent. In this method, a mixture of 45 {mu}L chloroform (extraction solvent) and 450 {mu}L tetrahydrofuran (dispersive solvent) is rapidly injected by syringe into a 5 mL aqueous sample containing 3% (w/v) sodium chloride and an appropriate amount of the Schiff's base. As a result, a cloudy solution is formed by entire dispersion of the extraction solvent into the aqueous phase. After centrifuging for 5 min at 5000 rpm, the sedimented phase is directly injected into the electrothermal atomic absorption spectrometry for Ni(II) determination. Some important parameters, such as kind and volume of extraction and dispersive solvents, extraction time, salt effect, pH and concentration of the chelating agent have been optimized. Under the optimum conditions, the enrichment factor for the presented method is 138. The calibration curve was linear over a nickel concentration range of 10-50 ng mL{sup -1}. The detection limit and relative standard deviation were 0.04 ng mL{sup -1} and 2.1%, respectively. The method was successfully applied to the extraction and determination of Ni(II) in different water samples. - Highlights: Black-Right-Pointing-Pointer A new synthesized schiff's base was used for selective separation of Ni(II) ions. Black-Right-Pointing-Pointer The method based on DLLME was successfully applied to the determination of Ni(II). Black-Right-Pointing-Pointer A cloudy solution is formed by entire dispersion of the extraction solvent into the aqueous phase. Black-Right-Pointing-Pointer In this work, the response surface analysis was used for the optimization purpose. Black-Right-Pointing-Pointer The curvature of response surface reflects the interactive effect of the variables.

  18. Velocity-resolved [{\\rm{C}}\\,{\\rm{II}}] Emission from Cold Diffuse Clouds in the Interstellar Medium

    Science.gov (United States)

    Goldsmith, Paul F.; Pineda, Jorge L.; Neufeld, David A.; Wolfire, Mark G.; Risacher, Christophe; Simon, Robert

    2018-04-01

    We have combined emission from the 158 μm fine structure transition of C+ observed with the GREAT and upGREAT instruments on SOFIA with 21 cm absorption spectra and visual extinction to characterize the diffuse interstellar clouds found along the lines of sight. The weak [C II] emission is consistent in velocity and line width with the strongest H I component produced by the cold neutral medium. The H I column density and kinetic temperature are known from the 21 cm data and, assuming a fractional abundance of ionized carbon, we calculate the volume density and thermal pressure of each source, which vary considerably, with 27 {cm}}-3≤slant n({{{H}}}0) ≤slant 210 cm‑3 considering only the atomic hydrogen along the lines of sight to be responsible for the C+, while 13 {cm}}-3≤slant n({{{H}}}0+{{{H}}}2)≤slant 190 cm‑3 including the hydrogen in both forms. The thermal pressure varies widely with 1970 cm‑3 K ≤slant {P}th}/k≤slant 10,440 cm‑3 K for H0 alone and 750 cm‑3 K ≤ P th/k ≤ 9360 cm‑3 K including both H0 and H2. The molecular hydrogen fraction varies between 0.10 and 0.67. Photoelectric heating is the dominant heating source, supplemented by a moderately enhanced cosmic ray ionization rate, constrained by the relatively low 45 K to 73 K gas temperatures of the clouds. The resulting thermal balance for the two lower-density clouds is satisfactory, but for the two higher-density clouds, the combined heating rate is insufficient to balance the observed C+ cooling.

  19. Direct Detection of Oxygen Ligation to the Mn4Ca Cluster of Photosystem II by X-ray Emission Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Pushkar, Yulia; Long, Xi; Glatzel, Pieter; Brudvig, Gary W.; Dismukes, G. Charles; Collins, Terrence J.; Yachandra, Vittal K.; Yano, Junko; Bergmann, Uwe

    2009-06-16

    Ligands play critical roles during the catalytic reactions in metalloproteins through bond formation/breaking, protonation/deprotonation, and electron/spin delocalization. While there are well-defined element-specific spectroscopic handles, such as X-ray spectroscopy and EPR, to follow the chemistry of metal catalytic sites in a large protein matrix, directly probing particular ligand atoms like C, N, and O is challenging due to their abundance in the protein. FTIR/Raman and ligand-sensitive EPR techniques such as ENDOR and ESEEM have been applied to study metal-ligand interactions. X-ray absorption spectroscopy (XAS) can also indirectly probe the ligand environment; its element-specificity allows us to focus only on the catalytic metal site, and EXAFS and XANES provide metal-ligand distances, coordination numbers, and symmetry of ligand environments. However, the information is limited, since one cannot distinguish among ligand elements with similar atomic number (i.e. C, N. and O). As an alternative and a more direct method to probe the specific metal-ligand chemistry in the protein matrix, we investigated the application of X-ray emission spectroscopy (XES). Using this technique we have identified the oxo-bridging ligands of the Mn{sub 4}Ca complex of photosystem II (PS II), a multisubunit membrane protein, that catalyzes the water oxidizing reaction. The catalytic mechanism has been studied intensively by Mn XAS. The fundamental question of this reaction, however, is how the water molecules are ligated to the Mn{sub 4}Ca cluster and how the O-O bond formation occurs before the evolution of O{sub 2}. This implies that it is necessary to follow the chemistry of the oxygen ligands in order to understand the mechanism.

  20. CONSTRAINING VERY HIGH MASS POPULATION III STARS THROUGH He II EMISSION IN GALAXY BDF-521 AT z = 7.01

    Energy Technology Data Exchange (ETDEWEB)

    Cai, Zheng; Fan, Xiaohui; Davé, Romeel; Zabludoff, Ann [Steward Observatory, University of Arizona, Tucson, AZ 85721 (United States); Jiang, Linhua [Kavli Institute for Astronomy and Astrophysics, Peking University, Beijing 100871 (China); Oh, S. Peng [Department of Physics, University of California, Broida Hall, Santa Barbara, CA 93106-9530 (United States); Yang, Yujin, E-mail: caiz@email.arizona.edu [Argelander-Institut fuer Astronomie, Auf dem Huegel 71, D-53121 Bonn (Germany)

    2015-01-30

    Numerous theoretical models have long proposed that a strong He II λ1640 emission line is the most prominent and unique feature of massive Population III (Pop III) stars in high-redshift galaxies. The He II λ1640 line strength can constrain the mass and initial mass function (IMF) of Pop III stars. We use F132N narrowband filter on the Hubble Space Telescope's (HST) Wide Field Camera 3 to look for strong He II λ1640 emission in the galaxy BDF-521 at z = 7.01, one of the most distant spectroscopically confirmed galaxies to date. Using deep F132N narrowband imaging, together with our broadband imaging with F125W and F160W filters, we do not detect He II emission from this galaxy, but place a 2σ upper limit on the flux of 5.3×10{sup −19} erg s{sup −1} cm{sup −2}. This measurement corresponds to a 2σ upper limit on the Pop III star formation rate (SFR{sub PopIII}) of ∼0.2 M {sub ☉} yr{sup –1}, assuming a Salpeter IMF with 50 ≲ M/M {sub ☉} ≲ 1000. From the high signal-to-noise broadband measurements in F125W and F160W, we fit the UV continuum for BDF-521. The spectral flux density is ∼3.6×10{sup −11}×λ{sup −2.32} erg s{sup −1} cm{sup −2} Å{sup –1}, which corresponds to an overall unobscured SFR of ∼5 M {sub ☉} yr{sup –1}. Our upper limit on SFR{sub PopIII} suggests that massive Pop III stars represent ≲ 4% of the total star formation. Further, the HST high-resolution imaging suggests that BDF-521 is an extremely compact galaxy, with a half-light radius of 0.6 kpc.

  1. Ni(II) and Cu(II)

    Indian Academy of Sciences (India)

    Administrator

    ethylidene)-. 1,5-carbohydrazone and bis(1,2-dimethyl-1-hydroxyimino-2- ethylidene)-1,5-carbodihydrazone N4-macrocycles as precursors for vitamin B12 and coenzyme B12 models. D U WARAD, C D SATISH and CHANDRASEKHAR S BAJGUR.

  2. Cobalt(II), nickel(II), copper(II), zinc(II), cadmium(II) and dioxouranium(II) complexes of thiophene-2-aldehyde-4-phenyl-thiosemicarbazone

    International Nuclear Information System (INIS)

    Singh, Balwan; Misra, Harihar

    1986-01-01

    The present paper describes the synthesis and characterisation of thiophene-2-aldehyde-4-phenylthiosemicarbazone (TAPTSC) and its metal complexes with Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and UO(II). (author). 30 refs., 1 table

  3. A Search for Supernova Remnants with Infrared [FeII] Emission: A Study of NGC 6946 with the WIYN High Resolution Infrared Camera (WHIRC)

    Science.gov (United States)

    Bruursema, Justice; Meixner, Margaret; Long, Knox S.; Otsuka, Masaaki

    2018-01-01

    Supernovae and supernova remnants (SNRs) play an important role in the evolution of the interstellar medium of their host galaxies. To better understand this role, it will be necessary to obtain large samples of these objects and examine how their properties relate to their physical environments. In this study, we employ a relatively unexplored technique to identify large numbers of SNRs using both narrow and broadband infrared imaging. We used the WIYN High Resolution Infrared Camera (WHIRC) on the 3.5m WIYN telescope to image nearby galaxy NGC 6946 in broadbands J and H and narrowbands designed to measure 1.64 μm [Fe II] emission, and Paβ emission. The uniqueness of our method lies in the use of additional narrowband “off” filters, adjacent to the [Fe II] and Paβ filters, but offset by 4500 km s-1. The “off” filters and broadband filters provide the information needed to determine which objects are strongly emitting [Fe II]. Our final analysis resulted in the identification of 72 supernova remnant candidates (SNRcs) which we are confident are SNRs, however spectroscopic observations will be needed to confirm their classification. The strength of our results, as discussed below, gives us confidence that our [Fe II] emission search method is an effective way to locate SNRcs.

  4. Aplicación de Líquidos Iónicos para la hidroaminación homogénea de olefinas catalizada por Complejos de Ni(II

    Directory of Open Access Journals (Sweden)

    Edith Marcela Erira

    2009-04-01

    Full Text Available Los líquidos iónicos son excelentes medios para reacciones catalíticas, debido a que pueden ser utilizados para optimizar y/o reciclar los catalizadores homogéneos. En este trabajo se describe el uso de varios líquidos iónicos de bajo punto de fusión (-30 – -34 °C – basados en derivados de la piridina – para utilizarlos en la hidroaminación de olefinas activadas, catalizada por complejos de Ni(II. El catalizador [Ni(Pigiphos(NCCH3](ClO42 presenta buena actividad cuándo el medio de reacción es un líquido iónico (TON hasta 172 y el sistema catalizador/líquido iónico se puede reciclar por lo menos 2 veces.

  5. Crystal structures and characterization of two divalent metal selenates templated by dabco, (C6H14N2[MII(H2O6](SeO42 (MII: NiII, ZnII

    Directory of Open Access Journals (Sweden)

    Nouha Loulou Nkhili

    2017-05-01

    Full Text Available Two new organic–inorganic hybrid materials have been synthesized and crystallographically characterized. Both compounds, (C6H14N2[Ni(H2O6](SeO42 (I and (C6H14N2[Zn(H2O6](SeO42 (II, crystallize isotypically in the monoclinic system, space group P21/c, with the following unit cell parameters: a = 12.4045(3, b = 11.9360(3, c = 12.8366(3 Å, β = 108.518(2°, V = 1802.18(8 Å3, Z = 4 for compound (I and a = 12.7839(2, b = 11.9153(4, c = 12.3814(2 Å, β = 108.264(5°, V = 1790.97(7 Å3, Z = 4 for the zinc related phase. Their supramolecular structure consists of metallic cation octahedrally coordinated by six water molecules [MII(H2O6]2+, selenate anions (SeO42− and dabcodiium cation (C6H14N22+ linked together via two types of hydrogen bonds, Ow–H…O and N–H…O only. The thermal decomposition of these supramolecular compounds takes place in several steps leading to the formation of metal oxide. The magnetic measurements show that the nickel based compound is predominantly paramagnetic with weak antiferromagnetic interactions at low temperature.

  6. Synthesis, characterization, in-vitro antimicrobial properties, molecular docking and DFT studies of 3-{(E-[(4,6-dimethylpyrimidin-2-ylimino]methyl} naphthalen-2-ol and Heteroleptic Mn(II, Co(II, Ni(II and Zn(II complexes

    Directory of Open Access Journals (Sweden)

    Chioma Festus

    2018-03-01

    Full Text Available Heteroleptic divalent metal complexes [M(L (bipy(Y]•nH2O (where M = Mn, Co, Ni, and Zn; L = Schiff base; bipy = 2,2’-bipyridine; Y = OAc and n = 0, 1 have been synthesized from pyrimidine Schiff base ligand 3-{(E-[(4,6-dimethylpyrimidin-2-ylimino]methyl} naphthalen-2-ol, 2,2’-bipyridine and metal(II acetate salts. The Schiff base and its complexes were characterized by analytical (CHN elemental analyses, solubility, melting point, conductivity measurements, spectral (IR, UV-vis, 1H and 13C-NMR and MS and magnetometry. The elemental analyses, Uv-vis spectra and room temperature magnetic moment data provide evidence of six coordinated octahedral geometry for the complexes. The metal complexes’ low molar conductivity values in dimethylsulphoxide suggested that they were non-ionic in nature. The compounds displayed moderate to good antimicrobial and antifungal activities against S. aureus, P. aeruginosa, E. coli, B. cereus, P. mirabilis, K. oxytoca, A. niger, A. flevus and R. Stolonifer. The compounds also exhibited good antioxidant potentials with ferrous ion chelation and, 1-diphenyl-2-picryl-hydrazyl (DPPH radical scavenging assays. Molecular docking studies showed a good interaction with drug targets used. The structural and electronic properties of complexes were further confirmed by density functional theory calculations.

  7. Two emissive-magnetic composite platforms for Hg(II) sensing and removal: The combination of magnetic core, silica molecular sieve and rhodamine chemosensors

    Science.gov (United States)

    Mao, Hanping; Liu, Zhongshou

    2018-01-01

    In this paper, a composite sensing platform for Hg(II) optical sensing and removal was designed and reported. A core-shell structure was adopted, using magnetic Fe3O4 nanoparticles as the core, silica molecular sieve MCM-41 as the shell, respectively. Two rhodamine derivatives were synthesized as chemosensor and covalently immobilized into MCM-41 tunnels. Corresponding composite samples were characterized with SEM/TEM images, XRD analysis, IR spectra, thermogravimetry and N2 adsorption/desorption analysis, which confirmed their core-shell structure. Their emission was increased by Hg(II), showing emission turn on effect. High selectivity, linear working curves and recyclability were obtained from these composite samples.

  8. Two emissive-magnetic composite platforms for Hg(II) sensing and removal: The combination of magnetic core, silica molecular sieve and rhodamine chemosensors.

    Science.gov (United States)

    Mao, Hanping; Liu, Zhongshou

    2018-01-15

    In this paper, a composite sensing platform for Hg(II) optical sensing and removal was designed and reported. A core-shell structure was adopted, using magnetic Fe 3 O 4 nanoparticles as the core, silica molecular sieve MCM-41 as the shell, respectively. Two rhodamine derivatives were synthesized as chemosensor and covalently immobilized into MCM-41 tunnels. Corresponding composite samples were characterized with SEM/TEM images, XRD analysis, IR spectra, thermogravimetry and N 2 adsorption/desorption analysis, which confirmed their core-shell structure. Their emission was increased by Hg(II), showing emission turn on effect. High selectivity, linear working curves and recyclability were obtained from these composite samples. Copyright © 2017 Elsevier B.V. All rights reserved.

  9. A DEEP NARROWBAND IMAGING SEARCH FOR C iv AND He ii EMISSION FROM Lyα BLOBS

    International Nuclear Information System (INIS)

    Battaia, Fabrizio Arrigoni; Yang, Yujin; Hennawi, Joseph F.; Prochaska, J. Xavier; Matsuda, Yuichi; Yamada, Toru; Hayashino, Tomoki

    2015-01-01

    We conduct a deep narrowband imaging survey of 13 Lyα blobs (LABs) located in the SSA22 proto-cluster at z ∼ 3.1 in the C iv and He ii emission lines in an effort to constrain the physical process powering the Lyα emission in LABs. Our observations probe down to unprecedented surface brightness (SB) limits of (2.1–3.4) × 10 −18 erg s −1 cm −2 arcsec −2 per 1 arcsec 2 aperture (5σ) for the He ii λ1640 and C iv λ1549 lines, respectively. We do not detect extended He ii and C iv emission in any of the LABs, placing strong upper limits on the He ii/Lyα and C iv/Lyα line ratios, of 0.11 and 0.16, for the brightest two LABs in the field. We conduct detailed photoionization modeling of the expected line ratios and find that, although our data constitute the deepest ever observations of these lines, they are still not deep enough to rule out a scenario where the Lyα emission is powered by the ionizing radiation from an obscured active galactic nucleus. Our models can accommodate He ii/Lyα and C iv/Lyα ratios as low as ≃0.05 and ≃0.07, respectively, implying that one needs to reach SB as low as (1–1.5) × 10 −18 erg s −1 cm −2 arcsec −2  (at 5σ) in order to rule out a photoionization scenario. These depths will be achievable with the new generation of image-slicing integral field units such as the Multi Unit Spectroscopic Explorer (MUSE) on VLT and the Keck Cosmic Web Imager (KCWI). We also model the expected He ii/Lyα and C iv/Lyα in a different scenario, where Lyα emission is powered by shocks generated in a large-scale superwind, but find that our observational constraints can only be met for shock velocities v s ≳ 250 km s −1 , which appear to be in conflict with recent observations of quiescent kinematics in LABs

  10. A new synthesis of enantiomerically pure syn-(S)-β-hydroxy-α-amino acids via asymmetric aldol reactions of aldehydes with a homochiral Ni(II)-glycine/(S)-BPB Schiff base complex

    OpenAIRE

    Belokon, Yuri N.; Kochetkov, Konstantin A.; Ikonnikov, Nikolai S.; Strelkova, Tatiana V.; Harutyunyan, Syuzanna R.; Saghiyan, Ashot S.

    2001-01-01

    syn-(S)-β-Hydroxy-α-amino acids were synthesised stereoselectively via elaboration of the asymmetric aldol reactions of aldehydes with a chiral Ni(II)-(S)-BPB/glycine Schiff base complex in the presence of equimolar NaH in THF. The stereoselectivity of the reaction was studied as a function of time, the reaction conditions, the nature of the carbonyl compounds and the base used. The synthetic potential of this asymmetric method was demonstrated in the preparation of syn-(S)-β-hydroxyleucine o...

  11. Synthesis and stereochemical assignments of diastereomeric Ni(II complexes of glycine Schiff base with (R-2-(N-{2-[N-alkyl-N-(1-phenylethylamino]acetyl}aminobenzophenone; a case of configurationally stable stereogenic nitrogen

    Directory of Open Access Journals (Sweden)

    Hiroki Moriwaki

    2014-02-01

    Full Text Available A family of chiral ligands derived from α-phenylethylamine and 2-aminobenzophenone were prepared by alkylation of the nitrogen atom. Upon reaction with glycine and a Ni(II salt, these ligands were transformed into diastereomeric complexes, as a result of the configurational stability of the stereogenic nitrogen atom. Different diastereomeric ratios were observed depending on the substituent R introduced in the starting ligand, and stereochemical assignments were based on X-ray analysis, along with NMR studies and optical rotation measurements.

  12. Observation and resonant x-ray optical interpretation of multi-atom resonant photoemission effects in O 1s emission from NiO

    International Nuclear Information System (INIS)

    Mannella, N.; Yang, S.-H.; Mun, B.S.; Garcia de Abajo, F.J.; Kay, A.W.; Sell, B.C.; Watanabe, M.; Ohldag, H.; Arenholz, E.; Young, A.T.; Hussain, Z.; Van Hove, M.A.; Fadley, C.S.

    2006-01-01

    We present experimental and theoretical results for the variation of the O 1s intensity from a NiO(001) surface as the excitation energy is varied through the Ni 2p1/2,3/2 absorption resonances, and as the incidence angle of the radiation is varied from grazing to larger values. For grazing incidence, a strong multi-atom resonant photoemission(MARPE) effect is seen on the O 1s intensity as the Ni 2p resonances are crossed, but its magnitude decreases rapidly as the incidence angle is increased. Resonant x-ray optical (RXRO) calculations are found to predict these effects very well, although the experimental effects are found to decrease at higher incidence angles faster than those in theory. The potential influence of photoelectron diffraction effects on such measurements are also considered, including experimental data with azimuthal-angle variation and corresponding multiple-scattering-diffraction calculations, but we conclude that they do not vary beyond what is expected on the basis of the change in photoelectron kinetic energy. Varying from linear polarization to circular polarization is found to enhance these effects in NiO considerably, although the reasons are not clear. We also discuss the relationship of these measurements to other related interatomic resonance experiments and theoretical developments, and make some suggestions for future studies in this area

  13. Different Supramolecular Coordination Polymers of [N,N'-di(pyrazin-2-yl-pyridine-2,6-diamine]Ni(II with Anions and Solvent Molecules as a Result of Hydrogen Bonding

    Directory of Open Access Journals (Sweden)

    Hsin-Ta Wang

    2007-04-01

    Full Text Available Ni(II complexes of N,N'–di(pyrazin–2–ylpyridine–2,6–diamine (H2dpzpda with different anions were synthesized and their structures were determined by X-ray diffraction. Hydrogen bonds between the amino groups and anions assembled the mononuclear molecules into different architectures. The perchlorate complex had a 1-D chain structure, whereas switching the anion from perchlorate to nitrate resulted in a corresponding change of the supramolecular structure from 1-D to 3-D. When the nitrate complex packed with the co-crystallized water, a double chain structure was formed through hydrogen bonding. The magnetic studies revealed values of g = 2.14 and D = 3.11 cm-1 for [Ni(H2dpzpda2](ClO42 (1 and g = 2.18 and D = 2.19 cm-1 for [Ni(H2dpzpda2](NO32 (2, respectively.

  14. A HERSCHEL SURVEY OF THE [N II] 205 {mu}m LINE IN LOCAL LUMINOUS INFRARED GALAXIES: THE [N II] 205 {mu}m EMISSION AS A STAR FORMATION RATE INDICATOR

    Energy Technology Data Exchange (ETDEWEB)

    Zhao Yinghe; Gao Yu [Purple Mountain Observatory, Chinese Academy of Sciences, Nanjing 210008 (China); Lu, Nanyao; Xu, C. Kevin; Lord, S.; Howell, J.; Appleton, P.; Mazzarella, J.; Schulz, B. [Infrared Processing and Analysis Center, California Institute of Technology, MS 100-22, Pasadena, CA 91125 (United States); Isaak, K. G. [ESA Astrophysics Missions Division, ESTEC, PO Box 299, 2200 AG Noordwijk (Netherlands); Charmandaris, V. [Department of Physics and ITCP, University of Crete, GR-71003 Heraklion (Greece); Diaz-Santos, T.; Surace, J. [Spitzer Science Center, California Institute of Technology, MS 220-6, Pasadena, CA 91125 (United States); Evans, A. [Department of Astronomy, University of Virginia, 530 McCormick Road, Charlottesville, VA 22904 (United States); Iwasawa, K. [ICREA and Institut de Ciencies del Cosmos (ICC), Universitat de Barcelona (IEEC-UB), Marti i Franques 1, E-08028 Barcelona (Spain); Leech, J. [Department of Physics, University of Oxford, Denys Wilkinson Building, Keble Road, Oxford OX1 3RH (United Kingdom); Petric, A. O. [Astronomy Department, California Institute of Technology, Pasadena, CA 91125 (United States); Sanders, D. B. [Institute for Astronomy, University of Hawaii, 2680 Woodlawn Drive, Honolulu, HI 96822 (United States); Van der Werf, P. P., E-mail: yhzhao@ipac.caltech.edu [Leiden Observatory, Leiden University, PO Box 9513, 2300 RA Leiden (Netherlands)

    2013-03-01

    We present, for the first time, a statistical study of [N II] 205 {mu}m line emission for a large sample of local luminous infrared galaxies using Herschel Spectral and Photometric Imaging Receiver Fourier Transform Spectrometer (SPIRE FTS) data. For our sample of galaxies, we investigate the correlation between the [N II] luminosity (L{sub [N{sub II]}}) and the total infrared luminosity (L{sub IR}), as well as the dependence of L{sub [N{sub II]}}/L{sub IR} ratio on L{sub IR}, far-infrared colors (IRAS f{sub 60}/f{sub 100}), and the [O III] 88 {mu}m to [N II] luminosity ratio. We find that L{sub [N{sub II]}} correlates almost linearly with L{sub IR} for non-active galactic nucleus galaxies (all having L{sub IR} < 10{sup 12} L{sub Sun }) in our sample, which implies that L{sub [N{sub II]}} can serve as a star formation rate tracer which is particularly useful for high-redshift galaxies that will be observed with forthcoming submillimeter spectroscopic facilities such as the Atacama Large Millimeter/submillimeter Array. Our analysis shows that the deviation from the mean L{sub [N{sub II]}}-L{sub IR} relation correlates with tracers of the ionization parameter, which suggests that the scatter in this relation is mainly due to the variations in the hardness, and/or ionization parameter, of the ambient galactic UV field among the sources in our sample.

  15. FLARE-LIKE VARIABILITY OF THE Mg II {lambda}2800 EMISSION LINE IN THE {gamma}-RAY BLAZAR 3C 454.3

    Energy Technology Data Exchange (ETDEWEB)

    Leon-Tavares, J. [Finnish Centre for Astronomy with ESO (FINCA), University of Turku, Vaeisaelaentie 20, FI-21500 Piikkioe (Finland); Chavushyan, V.; Patino-Alvarez, V.; Carraminana, A.; Carrasco, L. [Instituto Nacional de Astrofisica Optica y Electronica (INAOE), Apartado Postal 51 y 216, 72000 Puebla (Mexico); Valtaoja, E. [Tuorla Observatory, Department of Physics and Astronomy, University of Turku, FI-20100 Turku (Finland); Arshakian, T. G. [I. Physikalisches Institut, Universitaet zu Koeln, Zuelpicher Str. 77, D-50937 Koeln (Germany); Popovic, L. C. [Astronomical Observatory, Volgina 7, 11160 Belgrade 74 (Serbia); Tornikoski, M.; Laehteenmaeki, A. [Aalto University Metsaehovi Radio Observatory, Metsaehovintie 114, FI-02540 Kylmaelae (Finland); Lobanov, A. [Max-Planck-Institut fuer Radioastronomie, Auf dem Huegel 69, D-53121 Bonn (Germany)

    2013-02-01

    We report the detection of a statistically significant flare-like event in the Mg II {lambda}2800 emission line of 3C 454.3 during the outburst of autumn 2010. The highest levels of emission line flux recorded over the monitoring period (2008-2011) coincide with a superluminal jet component traversing through the radio core. This finding crucially links the broad emission line fluctuations to the non-thermal continuum emission produced by relativistically moving material in the jet and hence to the presence of broad-line region clouds surrounding the radio core. If the radio core were located at several parsecs from the central black hole, then our results would suggest the presence of broad-line region material outside the inner parsec where the canonical broad-line region is envisaged to be located. We briefly discuss the implications of broad emission line material ionized by non-thermal continuum in the context of virial black hole mass estimates and gamma-ray production mechanisms.

  16. SYNTHESIS AND CHARACTERIZATION OF SALICYLALDAZINE AND ITS METAL (II) COMPLEXES DERIVED FROM METAL (II) CHLORIDES

    OpenAIRE

    Jamila wazir

    2016-01-01

    The salicylaldazine (ligand) and its metal (II) complexes like copper (II), nickel (II), zinc (II), cobalt (II) and manganese (II) complexes has been synthesized and characterized by different techniques using FTIR, UV-VIS spectroscopy. The ligand (salicylaldazine) is synthesized by the condensation reaction of salicylaldehyde and hydrazine sulfate. The salicylaldazine metal (II) complexes like Cu (II) , Ni(II), Zn (II), Co(II), Mn(II) were prepared by using metal (II) chloride in dioxane. Th...

  17. Modelling Plasticity of Ni3Al-Based L12 Intermetallic Single Crystals. II. Two-Step (T1) and T2) Deformation Behaviour (Postprint

    National Research Council Canada - National Science Library

    Choi, Y. S; Dimiduk, D. M; Uchic, M. D; Parthasarathy, T. A

    2007-01-01

    The two-step (T1 and T2) deformation behaviour of Ni3Al-based single crystals was modelled under the framework of a new constitutive model proposed by Y.S. Choi, D.M. Dimiduk, M.D. Uchic, et al. [Phil. Mag. 87 1939 (2007...

  18. Sepiolite functionalized with N-[3-(trimethoxysilylpropyl]-ethylenediamine triacetic acid trisodium salt. Part II: Sorption of Ni2+ from aqueous solutions

    Directory of Open Access Journals (Sweden)

    Lazarević Slavica S.

    2016-01-01

    Full Text Available sorption of Ni2+ on the sepiolite functionalized by covalent grafting of N-[3-(trimethoxysilylpropyl]ethylenediamine triacetic acid trisodium salt, MSEAS, was studied in batch experiments as a function of the initial metal concentration, the equilibration time, pH value, and temperature. The modification of sepiolite resulted in an enhanced Ni2+ retention with a capacity of 0.261 mmol/g at 298 K. The retention of Ni2+ ions occurred dominantly by specific sorption and exchange of Mg2+ ions from the sepiolite structure. The sorption process followed pseudo-second-order kinetics. The sorption equilibrium results were best described by the non-linear form of the Langmuir Sorption Equation. The values of the thermodynamic parameters (enthalpy, free energy and entropy were calculated from temperature dependent sorption isotherms and these values showed that the sorption of Ni2+ onto modified sepiolite was endothermic. [Projekat Ministarstva nauke Republike Srbije, br. III 45019 i FP7 NANOTECH FTM No. 245916

  19. Characterization modelling of aquatic ecotoxicity from metal emission to be applied in Life Cycle Impact Assessment

    DEFF Research Database (Denmark)

    Dong, Yan

    on bioavailability. However, ecotoxicity of several metals that commonly appear in Life Cycle Inventory (LCI) have not yet been characterized in freshwater by the novel method. Ecotoxicity CF in marine ecosystem has received even less attention. In the previous Life Cycle Impact Assessment (LCIA) model, marine CF...... speciation varies in different water chemistries. Thus for each metal spatially differentiated freshwater CF was developed in seven different EU freshwater archetypes. Considering that emission location is often unknown in Life Cycle Assessment (LCA) studies, different averaging principles were tested...... mentioned above, this Ph.D. project aims at developing aquatic CFs for metals, including freshwater CF for 14 metals (Al(III), Ba, Be, Cd, Co, Cr(III), Cs, Cu(II), Fe(II), Fe(III), Mn(II), Ni, Pb, Sr and Zn) and marine CF for nine metals (Cd, Co, Cr(III), Cu, Fe(III), Mn, Ni, Pb and Zn) both for emission...

  20. TransCom N2O model inter-comparison, Part II : Atmospheric inversion estimates of N2O emissions

    NARCIS (Netherlands)

    Thompson, R. L.; Ishijima, K.; Saikawa, E.; Corazza, M.; Karstens, U.; Patra, P. K.; Bergamaschi, P.; Chevallier, F.; Dlugokencky, E.; Prinn, R. G.; Weiss, R. F.; O'Doherty, S.; Fraser, P. J.; Steele, L. P.; Krummel, P. B.; Vermeulen, A.; Tohjima, Y.; Jordan, A.; Haszpra, L.; Steinbacher, M.; Van Der Laan, S.; Aalto, T.; Meinhardt, F.; Popa, Maria Elena; Moncrieff, J.; Bousquet, P.

    2014-01-01

    This study examines N2O emission estimates from 5 different atmospheric inversion frameworks. The 5 frameworks differ in the choice of atmospheric transport model, meteorological data, prior uncertainties and inversion method but use the same prior emissions and observation dataset. The mean

  1. CRITERIA POLLUTANT EMISSIONS FROM INTERNAL COMBUSTION ENGINES IN THE NATURAL GAS INDUSTRY VOLUME II. APPENDICES A-I

    Science.gov (United States)

    The report summarizes emission factors for criteria pollutants (NOx, CO, CH4, C2H6, THC, NMHC, and NMEHC) from stationary internal combustion engines and gas turbines used in the natural gas industry. The emission factors were calculated from test results from five test campaigns...

  2. Use of Aloe vera shell ash supported Ni0.5Zn0.5Fe2O4 magnetic nanoparticles for removal of Pb (II from aqueous solutions

    Directory of Open Access Journals (Sweden)

    Samira Namavari

    2016-03-01

    Full Text Available Background: Lead (Pb is a heavy metal that is widely utilized in industries. It contaminates soil and groundwater. Its non-biodegradability, severe toxicity, carcinogenicity, ability to accumulate in nature and contaminate groundwater and surface water make this toxic heavy metal extremely dangerous to living beings and the environment. Therefore, technical and economic methods of removing Pb are of great importance. This study evaluated the efficiency of Ni0.5Zn0.5Fe2O4 magnetic nanoparticles supported by Aloe vera shell ash in removing Pb from aqueous environments. Methods: The adsorbent was characterized by several methods, including x-ray diffraction (XRD, scanning electron microscopy (SEM, and Fourier transform infrared spectroscopy (FT-IR. Then, the potential of Aloe vera shell ash-supported Ni0.5Zn0.5Fe2O4 magnetic nanoparticles to adsorb Pb (II was investigated. To determine the amount of lead absorbed by this adsorbent, different pHs (2, 4, 5, and 6, adsorbent doses (0.01-0.40 g, Pb concentrations (5, 10, 20, 30, 40, 50, 60, 80, 100, 200, 300, and 600 mg/L, and exposure times (0, 5, 10, 15, 20, 30, 40, 50, and 60 minutes until reaching equilibrium were tested using an atomic absorption spectrometer (Varian-AA240FS. Residual concentrations of Pb were read. Results: The results show that a time of 15 minutes, pH value of 9, and adsorbent dose of 0.2 g are the optimum conditions for Pb (II removal by this adsorption process. Increasing the initial concentration of Pb (II from 5 to 600 mg/L decreased removal efficiency from 98.8% to 73%. The experimental data fit well into the Freundlich isotherm model (R2 = 0.989. Conclusion: Ni0.5Zn0.5Fe2O4 magnetic nanoparticles supported by Aloe vera shell ash comprise a low-cost, simple, and environmentally benign procedure. The maximum monolayer adsorption capacity based on the Langmuir isotherm (R2 = 0.884 is 47.2 mg g-1. The prepared magnetic adsorbent can be well dispersed in aqueous solutions and

  3. Effects of gasoline properties on exhaust emission and photochemical reactivity; Gasoline seijo ga haiki gas sosei, kokagaku hannosei ni oyobosu eikyo

    Energy Technology Data Exchange (ETDEWEB)

    Kumagai, R.; Usui, K.; Moriya, A.; Sato, M.; Nomura, T.; Sue, H. [Petroleum Energy Center, Advanced Technology and Research Institute, Tokyo (Japan)

    1997-10-01

    In order to investigate the effects of fuel properties on emissions, four passenger cars were tested under Japanese 11 and 10-15 modes using two series gasoline fuels. The test results suggest that the distillation property (T90) affects A/F ratio which in turn influences exhaust emissions. The results of regression analysis show that both ozone forming potential and air toxics are highly corrected with the composition of aromatic hydrocarbons in gasoline. 3 refs., 10 figs., 6 tabs.

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

    International Nuclear Information System (INIS)

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

    2011-01-01

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

  5. Multi-objective optimization of combustion, performance and emission parameters in a jatropha biodiesel engine using Non-dominated sorting genetic algorithm-II

    Science.gov (United States)

    Dhingra, Sunil; Bhushan, Gian; Dubey, Kashyap Kumar

    2014-03-01

    The present work studies and identifies the different variables that affect the output parameters involved in a single cylinder direct injection compression ignition (CI) engine using jatropha biodiesel. Response surface methodology based on Central composite design (CCD) is used to design the experiments. Mathematical models are developed for combustion parameters (Brake specific fuel consumption (BSFC) and peak cylinder pressure (Pmax)), performance parameter brake thermal efficiency (BTE) and emission parameters (CO, NO x , unburnt HC and smoke) using regression techniques. These regression equations are further utilized for simultaneous optimization of combustion (BSFC, Pmax), performance (BTE) and emission (CO, NO x , HC, smoke) parameters. As the objective is to maximize BTE and minimize BSFC, Pmax, CO, NO x , HC, smoke, a multiobjective optimization problem is formulated. Nondominated sorting genetic algorithm-II is used in predicting the Pareto optimal sets of solution. Experiments are performed at suitable optimal solutions for predicting the combustion, performance and emission parameters to check the adequacy of the proposed model. The Pareto optimal sets of solution can be used as guidelines for the end users to select optimal combination of engine output and emission parameters depending upon their own requirements.

  6. Update of progress for Phase II of B&W`s advanced coal-fired low-emission boiler system

    Energy Technology Data Exchange (ETDEWEB)

    McDonald, D.K. [Babcock & Wilcox, Barberton, OH (United States); Madden, D.A.; Rodgers, L.W. [Babcock & Wilcox, Alliance, OH (United States)] [and others

    1995-11-01

    Over the past five years, advances in emission control techniques at reduced costs and auxiliary power requirements coupled with significant improvements in steam turbine and cycle design have significantly altered the governing criteria by which advanced technologies have been compared. With these advances, it is clear that pulverized coal technology will continue to be competitive in both cost and performance with other advanced technologies such as Integrated Gasification Combined Cycle (IGCC) or first generation Pressurized Fluidized Bed Combustion (PFBC) technologies for at least the next decade. In the early 1990`s it appeared that if IGCC and PFBC could achieve costs comparable to conventional pulverized coal plants, their significantly reduced NO{sub x} and SO{sub 2} emissions would make them more attractive. A comparison of current emission control capabilities shows that all three technologies can already achieve similarly low emissions levels.

  7. Entrance- and exit-channel effects and the suppression of neutron emission from 64Ni+92Zr→/sup 156/Er/sup */

    International Nuclear Information System (INIS)

    Love, D.J.G.; Bishop, P.J.; Kirwan, A.; Nolan, P.J.; Thornley, D.J.; Nelson, A.H.; Twin, P.J.

    1986-01-01

    High--angular-momentum components have been found in the cross section for /sup 64/Ni+/sup 92/Zr→/sup 156/Er /sup */ by γ-ray spectroscopy. They are expected to influence the known low evaporation-neutron multiplicity. The feeding pattern rules out significant trapping in superdeformed states at low spin, an explanation previously advanced. Simple coupled-channels calculations are consistent with the observations. The statistical model with high-l fusion enhanced consistently with observation reproduces the neutron multiplicity satisfactorily

  8. Reactivity and neutron emission measurements of burnt PWR fuel rod samples in LWR-PROTEUS phase II

    International Nuclear Information System (INIS)

    Murphy, M. F.; Jatuff, F.; Grimm, P.; Seiler, R.; Brogli, R.; Meier, G.; Berger, H. D.; Chawla, R.

    2004-01-01

    Measurements have been made of the reactivity effects and the neutron emission rates of uranium oxide and mixed oxide burnt fuel samples having a wide range of burnup values and coming from a Pressurised Water Reactor (PWR). The reactivity measurements have been made in a PWR lattice moderated in turn with: water, a water and heavy water mixture, and water containing boron. An interesting relationship has been found between the neutron emission rate and the measured reactivity. (authors)

  9. Copper(II), cobalt(II), nickel(II) and zinc(II) complexes of Schiff base ...

    Indian Academy of Sciences (India)

    Unknown

    metal (II) complexes with Schiff bases, in the pre- sent paper we report the synthesis and characteriza- tion of Cu(II), Co(II), Ni(II) and Zn(II) complexes of Schiff base derived from the condensation of benzil-2,4-dinitrophenylhydrazone with aniline. The proposed structure of the complexes is shown in chart 1. 2. Experimental.

  10. Properties of z ~ 3-6 Lyman break galaxies. II. Impact of nebular emission at high redshift

    Science.gov (United States)

    de Barros, S.; Schaerer, D.; Stark, D. P.

    2014-03-01

    Context. To gain insight on the mass assembly and place constraints on the star formation history (SFH) of Lyman break galaxies (LBGs), it is important to accurately determine their properties. Aims: We estimate how nebular emission and different SFHs affect parameter estimation of LBGs. Methods: We present a homogeneous, detailed analysis of the spectral energy distribution (SED) of ~1700 LBGs from the GOODS-MUSIC catalogue with deep multi-wavelength photometry from the U band to 8 μm to determine stellar mass, age, dust attenuation, and star formation rate. Using our SED fitting tool, which takes into account nebular emission, we explore a wide parameter space. We also explore a set of different star formation histories. Results: Nebular emission is found to significantly affect the determination of the physical parameters for the majority of z ~ 3-6 LBGs. We identify two populations of galaxies by determining the importance of the contribution of emission lines to broadband fluxes. We find that ~65% of LBGs show detectable signs of emission lines, whereas ~35% show weak or no emission lines. This distribution is found over the entire redshift range. We interpret these groups as actively star-forming and more quiescent LBGs, respectively. We find that it is necessary to considerer SED fits with very young ages (electronic form at http://www.aanda.org

  11. Synthesis of unsymmetric bipyridine-Pt(II) -alkynyl complexes through post-click reaction with emission enhancement characteristics and their applications as phosphorescent organic light-emitting diodes.

    Science.gov (United States)

    Li, Yongguang; Tsang, Daniel Ping-Kuen; Chan, Carmen Ka-Man; Wong, Keith Man-Chung; Chan, Mei-Yee; Yam, Vivian Wing-Wah

    2014-10-13

    Two unsymmetric bipyridine-platinum(II)-alkynyl complexes have been synthesised by a post-click reaction. These metal complexes are found to exhibit emission enhancement properties. The photoluminescence quantum yield can be significantly increased from 0.03 in solution to 0.72 in solid-state thin films. Efficient solution-processable organic light-emitting diodes have been fabricated by utilizing these complexes as phosphorescent dopants. A high external quantum efficiency of up to 5.8% has been achieved. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  12. MOF-derived hollow NiO-ZnO composite micropolyhedra and their application in catalytic thermal decomposition of ammonium perchlorate

    Science.gov (United States)

    Yang, Ji-Min

    2017-07-01

    Ni(II)-doped Zn-based coordination polymer particles (Ni(II)-doped Zn-CPPs) with controllable shape and size were successfully synthesized by solvothermal method, which further transformed to porous ZnO-NiO composite micropolyhedra without significant alterations in shape by calcination in air. Those products were characterized by powder X-ray diffraction (XRD), field emission scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), infrared spectroscopy (IR) and gas adsorption measurements. The catalytic activity of ZnO-NiO composites for the thermal decomposition of ammonium perchlorate (AP) was investigated. The result shows that all ZnO-NiO composites efficiently catalyzed the thermal decomposition of AP, and NiO-ZnO composite hollow octahedrons have the highest catalytic efficiency compared with that of most materials reported to now, indicating that porous ZnO-NiO composite micropolyhedra could be a promising candidate material for application in AP-based propellant.

  13. CME Expansion as the Driver of Metric Type II Shock Emission as Revealed by Self-consistent Analysis of High-Cadence EUV Images and Radio Spectrograms

    Science.gov (United States)

    Kouloumvakos, A.; Patsourakos, S.; Hillaris, A.; Vourlidas, A.; Preka-Papadema, P.; Moussas, X.; Caroubalos, C.; Tsitsipis, P.; Kontogeorgos, A.

    2014-06-01

    On 13 June 2010, an eruptive event occurred near the solar limb. It included a small filament eruption and the onset of a relatively narrow coronal mass ejection (CME) surrounded by an extreme ultraviolet (EUV) wave front recorded by the Solar Dynamics Observatory's (SDO) Atmospheric Imaging Assembly (AIA) at high cadence. The ejection was accompanied by a GOES M1.0 soft X-ray flare and a Type-II radio burst; high-resolution dynamic spectra of the latter were obtained by the Appareil de Routine pour le Traitement et l'Enregistrement Magnetique de l'Information Spectral (ARTEMIS IV) radio spectrograph. The combined observations enabled a study of the evolution of the ejecta and the EUV wave front and its relationship with the coronal shock manifesting itself as metric Type-II burst. By introducing a novel technique, which deduces a proxy of the EUV compression ratio from AIA imaging data and compares it with the compression ratio deduced from the band-split of the Type-II metric radio burst, we are able to infer the potential source locations of the radio emission of the shock on that AIA images. Our results indicate that the expansion of the CME ejecta is the source for both EUV and radio shock emissions. Early in the CME expansion phase, the Type-II burst seems to originate in the sheath region between the EUV bubble and the EUV shock front in both radial and lateral directions. This suggests that both the nose and the flanks of the expanding bubble could have driven the shock.

  14. Mn(II), Zn(II) and VO(II) Schiff

    Indian Academy of Sciences (India)

    Home; Journals; Journal of Chemical Sciences; Volume 113; Issue 3. Synthesis and characterisation of Cu(II), Ni(II), Mn(II), Zn(II) and VO(II) Schiff base complexes derived from o-phenylenediamine and acetoacetanilide. N Raman Y Pitchaikani Raja A Kulandaisamy. Inorganic Volume 113 Issue 3 June 2001 pp 183-189 ...

  15. Determination of HCl and VOC Emission from Thermal Degradation of PVC in the Absence and Presence of Copper, Copper(II) Oxide and Copper(II) Chloride

    OpenAIRE

    Jafari, Ahamad J.; Donaldson, John D.

    2009-01-01

    Polyvinyl chloride (PVC) has played a key role in the development of the plastic industry over the past 40 years. Thermal degradation of PVC leads to formation of many toxic pollutants such as HCl, aromatic and volatile organic carbon vapors. Thermal degradation of PVC and PVC in the present of copper, cupric oxide and copper(II) chloride were investigated in this study using a laboratory scale electrical furnace. HCl and Cl- ion were analyzed by a Dionex ion chromatograph and VOCs compounds ...

  16. Changes of inflammatory cells in rat lungs exposed to diesel emissions; Diesel haiki bakuro ni yoru rat hai no ensho saibo no henka

    Energy Technology Data Exchange (ETDEWEB)

    Kato, A. [Japan Automobile Research Institute Inc., Tsukuba (Japan); Kagawa, J. [Tokyo Women`s Medical College, Tokyo (Japan)

    1998-05-01

    Study was made on the effect of exposure to diesel emissions on inflammatory cells in a rat lungs. Four kinds of exposure gases with different contents of NO2 and particulate were prepared by diluting diesel emissions. Rats were exposed to diluted diesel emissions for 24 months, and inflammatory cells were detected morphologically in light microscopic and TEM specimens. As a result, particle-laden- alveolar macrophages increased dose- and time-dependently into the submucosa of intrapulmonary bronchioles, alveolar spaces and interstitume of alveolar walls, and bronchoassociated lymphatic tissues. Mast cells infiltrated into the interspaces of epithelial cells in airways. In the submucosa of the terminal bronchioles and the interstitume of alveolar walls, some sorts of inflammatory cells such as mast cells, plasma cells, neutrophils and lymphocytes infiltrated, and some cells showed cell-to-cell contacts. However, the airways were rarely injured by infiltration of inflammatory cells except for a fibrotic change. 2 refs., 2 figs., 2 tabs.

  17. NEW MASER EMISSION FROM NONMETASTABLE AMMONIA IN NGC 7538. II. GREEN BANK TELESCOPE OBSERVATIONS INCLUDING WATER MASERS

    Energy Technology Data Exchange (ETDEWEB)

    Hoffman, Ian M. [St. Paul' s School, Concord, NH 03301 (United States); Seojin Kim, Stella, E-mail: ihoffman@sps.edu [Current address: Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139 (United States)

    2011-12-15

    We present new maser emission from {sup 14}NH{sub 3} (9,6) in NGC 7538. Our observations include the known spectral features near v{sub LSR} = -60 km s{sup -1} and -57 km s{sup -1} and several more features extending to -46 km s{sup -1}. In three epochs of observation spanning two months we do not detect any variability in the ammonia masers, in contrast to the >10-fold variability observed in other {sup 14}NH{sub 3} (9,6) masers in the Galaxy over comparable timescales. We also present observations of water masers in all three epochs for which emission is observed over the velocity range -105 km s{sup -1} < v{sub LSR} < -4 km s{sup -1}, including the highest velocity water emission yet observed from NGC 7538. Of the remarkable number of maser species in IRS 1, H{sub 2}O and, now, {sup 14}NH{sub 3} are the only masers known to exhibit emission outside of the