Home About us Contact
|
Home About us Contact | ||
|
|
||
Liquid Phase (liquid + phase)
Kinds of Liquid Phase Terms modified by Liquid Phase Selected AbstractsMolecular Magnets: Deposition of Functionalized Cr7Ni Molecular Rings on Graphite from the Liquid Phase (Adv. Funct.ADVANCED FUNCTIONAL MATERIALS, Issue 10 2010Mater. [source] Deposition of Functionalized Cr7Ni Molecular Rings on Graphite from the Liquid PhaseADVANCED FUNCTIONAL MATERIALS, Issue 10 2010Alberto Ghirri Abstract Graphite is a clean substrate and its nanostructures hold great potential for applications. Anchoring large molecules on graphite represents a challenge for several reasons that essentially rise from the planar bonds of the packed honeycomb structure of carbon. Here, a systematic investigation by AFM and XPS on different derivatives of molecular Cr7Ni rings deposited on highly oriented pyrolytic graphite (HOPG) is reported. Cr7Ni is emerging as a prototipical example of molecular antiferromagnet on which quantum phenomena and coherence have been demonstrated. For the deposition of Cr7Ni on HOPG, two strategies are adopted: 1) Cr7Ni rings are functionalized with extended alkyl/benzene terminations and 2) a self-assembled monolayer of alkyl chains with sulfonate terminations is deposited and then a cationic Cr7Ni derivative is used. In both cases the electronic bond with the carbon surface is soft, but the two-step procedure is efficient, albeit indirect, in sticking molecular Cr7Ni on HOPG. These strategies can be easily extended to deposit other complex molecular aggregates on graphite from the liquid phase. [source] Development of a Supported Ionic Liquid Phase (SILP) Catalyst for Slurry-Phase Friedel,Crafts Alkylations of CumeneADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 3 2009J. Joni Abstract A supported ionic liquid phase (SILP) catalyst material has been developed based on a silica support coated with an acidic chloroaluminate ionic liquid. Compared to the results in a liquid-liquid biphasic reaction these materials showed in the isopropylation of cumene a clearly different selectivity which was found to be related to a reduction of the ionic liquid's acidity by the untreated silica support. By pretreating the support with a defined amount of ionic liquid for neutralization and removal of surface hydroxy groups, a well defined, very active and also very selective SILP catalyst for slurry phase Friedel,Crafts alkylation was obtained. [source] Bioreactors Based on Monolith-Supported Ionic Liquid Phase for Enzyme Catalysis in Supercritical Carbon DioxideADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 7 2007Pedro Lozano Abstract Bioreactors with covalently supported ionic liquid phases (SILP) were prepared as polymeric monoliths based on styrene,divinylbenzene or 2-hydroxyethyl methacrylate,ethylene dimethacrylate, and with imidazolium units loadings ranging from 54.7 to 39.8,% wt IL per gram of polymer. The SILPs were able to absorb Candida antarctica lipase B (CALB), leading to highly efficient and robust heterogeneous biocatalysts. The bioreactors were prepared as macroporous monolithic mini-flow systems and tested for the continuous flow synthesis of citronellyl propionate in supercritical carbon dioxide (scCO2) by transesterification. The catalytic activity of these mini-flow-bioreactors remained practically unchanged for seven operational cycles of 5,h each in different supercritical conditions. The best results were obtained when the most hydrophobic monolith, M-SILP- 8 -CALB, was assayed at 80,°C and 10,MPa, reaching a total turnover number (TON) of 35.8×104 mol product/mol enzyme. The results substantially exceeded those obtained for packed-bed reactors with supported silica-CALB-Si-4 catalyst under the same experimental conditions. [source] Effects of Electrode Protrusion Length, Pre-Existing Bubbles, Solution Conductivity and Temperature, on Liquid Phase Pulsed Electrical DischargePLASMA PROCESSES AND POLYMERS, Issue 11 2009Kai-Yuan Shih Abstract The effects of high voltage electrode needle protrusion length and the presence of low density pre-existing bubbles on liquid phase pulsed electrical discharge were investigated. Liquid phase pulsed corona discharge was operated with two different protrusion length needle electrodes (short , 2,mm and long , 20,mm) with different bulk solution conductivities (5,µS,·,cm,1 and 150,µS,·,cm,1) at room temperature (25,°C) and near boiling (95,°C). Chemical reactions formed in the discharge were also investigated by measuring the generation rates of hydrogen (H2), oxygen (O2) and hydrogen peroxide (H2O2). [source] Spectroscopic Properties in the Liquid Phase: Combining High-Level Ab Initio Calculations and Classical Molecular DynamicsCHEMPHYSCHEM, Issue 1 2006Michele Pavone Dr. Abstract We present an integrated computational tool, rooted in density functional theory, the polarizable continuum model, and classical molecular dynamics employing spherical boundary conditions, to study the spectroscopic observables of molecules in solution. As a test case, a modified OPLS-AA force field has been developed and used to compute the UV and NMR spectra of acetone in aqueous solution. The results show that provided the classical force fields are carefully reparameterized and validated, the proposed approach is robust and effective, and can also be used by nonspecialists to provide a general and powerful complement to experimental techniques. [source] Challenges in Measuring of Physical Properties of Liquid Phases for Material and Process Optimisation,ADVANCED ENGINEERING MATERIALS, Issue 4 2007S. Akbari The exact knowledge of thermo-physical properties of molten phases is crucial to modern metallurgy. It leads to optimized process windows including better metal/slag separation, suitable slag selection or reduced slag/refractory wetting. The most important properties are melting and boiling point, electrical- and thermal conductivity, melting and transition enthalpies, wetting angle, density, viscosity and surface tension. The aim of this paper is to present opportunities, methods and uncertainties of characterization of this kind of materials. This will be examplified by measuring three physical properties (density, viscosity and surface tension). [source] Effects of Electrode Protrusion Length, Pre-Existing Bubbles, Solution Conductivity and Temperature, on Liquid Phase Pulsed Electrical DischargePLASMA PROCESSES AND POLYMERS, Issue 11 2009Kai-Yuan Shih Abstract The effects of high voltage electrode needle protrusion length and the presence of low density pre-existing bubbles on liquid phase pulsed electrical discharge were investigated. Liquid phase pulsed corona discharge was operated with two different protrusion length needle electrodes (short , 2,mm and long , 20,mm) with different bulk solution conductivities (5,µS,·,cm,1 and 150,µS,·,cm,1) at room temperature (25,°C) and near boiling (95,°C). Chemical reactions formed in the discharge were also investigated by measuring the generation rates of hydrogen (H2), oxygen (O2) and hydrogen peroxide (H2O2). [source] Molecular dynamics simulations of hydrotropic solubilization and self-aggregation of nicotinamideJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 7 2010Yong Cui Abstract Hydrotropy is a phenomenon where the presence of a large quantity of one solute enhances the solubility of another solute. The mechanism of this phenomenon remains elusive and a topic of debate. This study employed molecular dynamics simulation to investigate the hydrotropic mechanism of a model system consisting of a hydrotropic agent, nicotinamide (NA), a poorly water-soluble solute, PG-300995 (PG), and water. Our study demonstrates that NA and PG undergo significant aggregation in the aqueous solution, a result correlating closely to the self-aggregation of NA under the same conditions. The correlations are found both structurally and dynamically, suggesting that the self-aggregation of NA may be a prerequisite, or at least a major contributor, to its hydrotropic effects. The self-aggregation of NA allows the segregation of the hydrophobic solute from water, a key step to ease the energy increase to the system. Energetic evidences directly show that the hydrotropic solubilization is favored in the presence of NA aggregation. These results are in strong support of the molecular aggregation hypothesis for hydrotropic solubilization. Additionally, it is found that the restoration of water,water HBs from the interference of the NA and PG molecules plays an important role for the aggregation. The HBs between the solute and the hydrotrope may contribute, but is not vital, to the aggregation and hence the hydrotropic effects. The dynamic data confirm that the aggregates, while remain in liquid state, are much more active dynamically than a pure NA amorphous/liquid phase under the same temperature and pressure. By equilibrating an NA amorphous agglomerate with water, it is found that the aggregation state, rather than an NA,water two phase system, is the equilibrium state of the NA,+,water system. © 2010 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:3048,3059, 2010 [source] Motional smearing of electrically recovered couplings measured from multipulse transientsCONCEPTS IN MAGNETIC RESONANCE, Issue 3 2001Scott A. Riley Abstract The measurement of residual dipolar and quadrupolar coupling constants in the liquid phase by using an electric field to destroy the isotropic nature of molecular tumbling is complicated by charge-induced turbulent motion. In many cases this motion is due to charge injection at electrode surfaces, an effect that leads to an apparent removal of electrically recovered anisotropic spectral splittings when measured from a spin-echo envelope modulation produced by a train of radio frequency (rf) pulses. To understand this averaging, the effect of quadrupolar couplings and enhanced molecular diffusion on free-induction, spin-echo, and Carr,Purcell signals is analytically determined in the special case of homogeneous rf pulses. Additional signal damping due to rf inhomogeneity and coupling constant heterogeneity is determined by numerically extending the kernel formalism introduced by Herzog and Hahn to understand spin diffusion in solids. Finally, the merit of the numerical approach is tested by comparison with analytical results for homogeneous rf pulses and experimental results for perdeuterated nitrobenzene involving inhomogeneous rf pulses and coupling heterogeneity. © 2001 John Wiley & Sons, Inc. Concepts Magn Reson 13: 171,189, 2001 [source] Growth and optical characterization of cerium and lead-doped Bi12TiO20 sillenite single crystalsCRYSTAL RESEARCH AND TECHNOLOGY, Issue 9 2005J. F. Carvalho Abstract Bi12TiO20 (BTO) single crystals doped with PbO and CeO2 were grown by the Top Seeded Solution Growth (TSSG) technique from the liquid phase with nominal compositions of 10Bi2O3 : (1,x)TiO2 : x PbO and 10Bi2O3 : (1,x)TiO2 : xCeO2 with x = 0.25 and 0.10. No growth-related difficulties were encountered other than those typical of sillenite crystals. Samples with good optical quality were obtained and were characterized by optical absorption, dark current, spectral photocurrent dependence, optical activity and electro-optic coefficient measurements. A comparison is made of the results of the optical measurements of doped and undoped BTO crystals. (© 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Identification of Chiral cis- and trans- 2-Stannyloxazolidines by Their NMR Spectra and Solid-State StructuresEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 20 2004Jean-Christophe Cintrat Abstract The assignment of cis and trans configurations in N -protected 4-substituted 2-tributylstannyl-1,3-oxazolidines by NMR has been achieved through the use of extrapolations of Karplus,Kitching-type relationships for 3J(119Sn,C,Z,13C) to establish the shape of the oxazolidine ring. Examination of 3J(H,H) allowed the determination of torsion angles for the substituents on C4 and C5, discrimination being completed by comparison of the H2 chemical shifts, together with the 2J(Sn,C,H2) values. The validity of the method was subsequently corroborated by comparison of the results obtained for the liquid phase with those obtained from radiocrystallographic structures of triphenylstannyl analogues or DFT calculations on trimethylstannyl analogues. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) [source] Evaluation of Transient Liquid Phase Bonding Between Titanium and SteelADVANCED ENGINEERING MATERIALS, Issue 7 2009Ahmed Elrefaey An investigation of microstructural development in transient liquid phase (TLP) bonds between commercially pure titanium and low carbon steel is presented in this study. Changes in the joint region and surrounding substrates were examined as a function of holding time at temperatures of 870 and 910 °C. Both interfacial microstructures and mechanical properties of brazed joints were investigated to evaluate joint quality. [source] Pedotransfer functions for solute transport parameters of Portuguese soilsEUROPEAN JOURNAL OF SOIL SCIENCE, Issue 4 2001M. C. Gonc, alves Summary The purpose of this study is to quantify solute transport parameters of fine-textured soils in an irrigation district in southern Portugal and to investigate their prediction from basic soil properties and unsaturated hydraulic parameters. Solute displacement experiments were carried out on 24 undisturbed soil samples by applying a 0.05 m KCl pulse during steady flow. The chloride breakthrough curves (BTCs) were asymmetric, with early breakthrough and considerable tailing characteristic of non-equilibrium transport. The retardation factor (R), dispersion coefficient (D), partitioning coefficient (,), and mass transfer coefficient (,) were estimated by optimizing the solution of the non-equilibrium convection,dispersion equation (CDE) to the breakthrough data. The solution could adequately describe the observed data as proved by a median of 0.972 for the coefficient of determination (r2) and a median for the mean squared error (MSE) of 5.1 × 10,6. The median value for R of 0.587 suggests that Cl, was excluded from a substantial part of the liquid phase. The value for , was typically less than 0.5, but the non-equilibrium effects were mitigated by a large mass transfer coefficient (, > 1). Pedotransfer functions (PTFs) were developed with regression and neural network analyses to predict R, D, , and , from basic soil properties and unsaturated hydraulic parameters. Fairly accurate predictions could be obtained for logD (r2 , 0.9) and , (r2 , 0.8). Prediction for R and log, were relatively poor (r2 , 0.5). The artificial neural networks were all somewhat more accurate than the regression equations. The networks are also more suitable for predicting transport parameters because they require only three input variables, whereas the regression equations contain many predictor variables. [source] Thermodynamic Investigation of Alkali-Metal-Induced High Temperature Embrittlement in Al-Li Alloys,ADVANCED ENGINEERING MATERIALS, Issue 11 2007S. Zhang Alkali metals are undesirable impurity elements in aluminum-lithium alloys. Despite their trace amount, they lead to high temperature embrittlement (HTE). In the present work, the results of a thermodynamic investigation are presented to elucidate its mechanism and compared with available experimental data. HTE arises from an intergranular alkali-metal-rich liquid phase that segregates into grain boundaries from the matrix and significantly weakens their strength. A new model is developed to describe the tendency of HTE, which shows grain refinement can decrease the tendency. [source] Deposition of Functionalized Cr7Ni Molecular Rings on Graphite from the Liquid PhaseADVANCED FUNCTIONAL MATERIALS, Issue 10 2010Alberto Ghirri Abstract Graphite is a clean substrate and its nanostructures hold great potential for applications. Anchoring large molecules on graphite represents a challenge for several reasons that essentially rise from the planar bonds of the packed honeycomb structure of carbon. Here, a systematic investigation by AFM and XPS on different derivatives of molecular Cr7Ni rings deposited on highly oriented pyrolytic graphite (HOPG) is reported. Cr7Ni is emerging as a prototipical example of molecular antiferromagnet on which quantum phenomena and coherence have been demonstrated. For the deposition of Cr7Ni on HOPG, two strategies are adopted: 1) Cr7Ni rings are functionalized with extended alkyl/benzene terminations and 2) a self-assembled monolayer of alkyl chains with sulfonate terminations is deposited and then a cationic Cr7Ni derivative is used. In both cases the electronic bond with the carbon surface is soft, but the two-step procedure is efficient, albeit indirect, in sticking molecular Cr7Ni on HOPG. These strategies can be easily extended to deposit other complex molecular aggregates on graphite from the liquid phase. [source] Liquid-Phase Exfoliation of Nanotubes and GrapheneADVANCED FUNCTIONAL MATERIALS, Issue 23 2009Jonathan N. Coleman Abstract Many applications of carbon nanotubes require the exfoliation of the nanotubes to give individual tubes in the liquid phase. This requires the dispersion, exfoliation, and stabilization of nanotubes in a variety of liquids. In this paper recent work in this area is reviewed, focusing on results from the author's group. It begins by reviewing stabilization mechanisms before exploring research into the exfoliation of nanotubes in solvents, by using surfactants or biomolecules and by covalent attachment of molecules. The concentration dependence of the degree of exfoliation in each case will be highlighted. In addition research into the dispersion mechanism for each dispersant type is discussed. Most importantly, dispersion quality metrics for all dispersants are compared. From this analysis, it is concluded that functionalized nanotubes can be exfoliated to the greatest degree. Finally, the extension of this work to the liquid phase exfoliation of graphite to give graphene is reviewed. [source] Anhydrous Polymeric Proton Conductors Based on Imidazole Functionalized PolysiloxaneFUEL CELLS, Issue 3-4 2006G. Scharfenberger Abstract Intrinsically proton conducting polymers with imidazole as proton solvent tethered to a polysiloxane backbone via a flexible spacer have been synthesized. Apart from the standard characterization also their thermal properties and transport behavior have been investigated. The materials exhibit proton conductivity as a consequence of self-dissociation of the imidazole moieties and "structure diffusion" of the resulting defects. In particular, no liquid phase such as water or monomeric imidazole is needed for the observed proton conductivities. To study the influence of the tether structure on the transport properties, cyclic oligomers and open chain polymers with different spacer lengths have been synthesized. The materials are thermally stable up to 200,°C and become soft around room temperature. The conductivity exhibits VTF and WLF behavior with maximum conductivities around ,,=,1.5.10,3,S,cm,1 at T,=,160,°C. The activation volume of the conductivity as derived from pressure dependent measurements is found to be unusually high. The lowest activation volumes and the highest conductivities are observed for the materials with the highest segmental mobilities, i.e. the longest spacers. Proton self-diffusion coefficients as obtained from PFG NMR diffusion measurements are significantly higher than expected from the proton conductivities obtained by dielectric spectroscopy. This corresponds to unusually high Haven ratios which have been interpreted by correlated proton transfers allowing for fast proton diffusion while minimizing the separation of ionic charge carriers. [source] Br/Cl signature of hydrothermal fluids: liquid,vapour fractionation of bromine revisitedGEOFLUIDS (ELECTRONIC), Issue 2 2006A. LIEBSCHER Abstract Br/Cl ratios of hydrothermal fluids are widely used as geochemical tracers in marine hydrothermal systems to prove fluid phase separation processes. However, previous results of the liquid,vapour fractionation of bromine are ambiguous. Here we report new experimental results of the liquid,vapour fractionation of bromine in the system H2O,NaCl,NaBr at 380,450°C and 22.9,41.7 MPa. Our data indicate that bromine is generally more enriched than chlorine in the liquid phase. Calculated exchange coefficients KD(Br-Cl)liquid-vapour for the reaction Brvapour + Clliquid = Brliquid + Clvapour are between 0.94 ± 0.08 and 1.66 ± 0.14 within the investigated P,T range. They correlate positively with DClliquid-vapour and suggest increasing bromine,chlorine fractionation with increasing opening of the liquid,vapour solvus, i.e. increasing distance to the critical curve in the H2O,NaCl system. An empirical fit of the form KD(Br-Cl)liquid-vapour = a*ln[b*(DClliquid-vapour,1) + e1/a] yields a = 0.349 and b = 1.697. Based on this empirical fit and the well-constrained phase relations in the H2O,NaCl system we calculated the effect of fluid phase separation on the Br/Cl signature of a hydrothermal fluid with initial seawater composition for closed and open adiabatic ascents along the 4.5 and 4.8 J g,1 K,1 isentropes. The calculations indicate that fluid phase separation can significantly alter the Br/Cl ratio in hydrothermal fluids. The predicted Br/Cl evolutions are in accord with the Br/Cl signatures in low-salinity vent fluids from the 9 to 10°N East Pacific Rise. [source] Broadband Nonlinear Optical Response of Graphene DispersionsADVANCED MATERIALS, Issue 23 2009Jun Wang A series of unoxidized and defect-free graphene dispersions with large populations of single and multilayer graphenes is prepared by employing high-yield exfoliation of graphene in the liquid phase. The graphene dispersions exhibit broadband optical limiting at 532 and 1064,nm. Nonlinear scattering, originated from the thermally induced solvent bubbles and microplasmas, is responsible for this nonlinear behavior. [source] Modelling of hygro-thermal behaviour and damage of concrete at temperature above the critical point of waterINTERNATIONAL JOURNAL FOR NUMERICAL AND ANALYTICAL METHODS IN GEOMECHANICS, Issue 6 2002D. Gawin Abstract In this paper, a model for the analysis of the behaviour of concrete at temperature largely exceeding critical point of water, is presented. In this temperature range liquid phase, i.e. capillary phase, and gas phase cannot be distinguished and only the latter exists. Consequently, capillary pressure has no more physical meaning above this point and liquid water is present only as physically adsorbed water. In this work, we give a different physical interpretation to the capillary pressure and use it still for the description of the hygrometric state of concrete in the zone, where temperature exceeds the critical point of water. Considerable thermal dilatation of the liquid water and the real behaviour of water vapour close to critical temperature are taken into account. Moreover, a special switching procedure in order to avoid the Stefan-like problem, which subsequently arises, is described and employed in the calculations. Finally, several numerical examples demonstrating the robustness of the adopted solution have been shown. Copyright © 2002 John Wiley & Sons, Ltd. [source] A Chemical Route to BiNbO4 CeramicsINTERNATIONAL JOURNAL OF APPLIED CERAMIC TECHNOLOGY, Issue 2 2009Oleg A. Shlyakhtin The liquid phase sintering of fine BiNbO4 powders allows to obtain dense ceramics with excellent microwave dielectric properties (,=44,46; Q×f=16,500,21,600 GHz) at T,700°C. The thermal decomposition of freeze-dried precursors results in the crystallization of a metastable ,,-BiNbO4 polymorph that transforms into a stable orthorhombic ,-modification at T,700°C. The dependence of sinterability on the powder synthesis temperature shows the maximum at 600°C, corresponding to the formation of crystalline BiNbO4 powders with a grain size 80,100 nm. Sintering temperature reduction to 700°C prevents the deterioration of silver contacts during co-firing with BiNbO4 ceramics. In situ scanning electron microscopy observation of the morphological evolution during sintering shows that the intense shrinkage soon after the appearance of a CuO,V2O5 eutectics-based liquid phase is accompanied by complete transformation of the ensemble of primary BiNbO4 particles. [source] Kinetics of the synthesis of propyl and butyl acrylates in the presence of some heteropolyacids as catalystsINTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 1 2009Jerzy Skrzypek Esterification reactions of acrylic acid with n -propanol and n -butanol were carried out in the liquid phase in the presence of H3PW12O40 or H3PMo12O40 as a catalyst, at various temperatures, molar ratios of the reactants, and concentrations of the catalyst. The kinetic equations had a nonelementary form. © 2008 Wiley Periodicals, Inc. Int J Chem Kinet 41: 12,17, 2009 [source] Quantum statistics of charged particles and fingerprints of wigner crystallization in D dimensionsINTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, Issue 15 2006N. H. March Abstract After a brief summary of the physical arguments underlying Wigner's original concept in 1934 of a quantal electron crystal, theoretical interpretation of a number of experimental findings are presented. These include (i) low-density carriers in semiconductors in applied magnetic fields in both three, and recently two, dimensions; and (ii) low-temperature phase diagram of underdoped high Tc cuprates; fullerides with relatively low Tc are also referred to in a related context. Interpretation of areas (i) and (ii) focuses on the relevance of both Fermi,Dirac and anyonic (fractional) statistics, the latter in relation to the proposed melting curve of the two-dimensional (2D) magnetically induced Wigner solid into the Laughlin liquid phase, which is the seat of the fractional quantum Hall effect. A brief discussion follows of crystalline phases additional to the Wigner solid, namely Skyrmion and Hall crystals. Bose,Einstein statistics is then referred to, but now in relation to finite-size confined quantal assemblies, with fingerprints of Wigner molecules the focus. Finally, quasi-1D lattices are considered, both in Bechgaard salts and in the very recent single-electron counting experiment of Bylander et al. © 2006 Wiley Periodicals, Inc. Int J Quantum Chem, 2006 [source] Importance of the Conditioning of the Chitosan Support in a Catalyst-Containing Ionic Liquid Phase Immobilised on Chitosan: The Palladium-Catalysed Allylation Reaction CaseADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 2-3 2010Renaud Moucel Abstract Catalysts containing ionic liquid phase immobilised on chitosan are successfully applied to the palladium-catalysed allylation reaction. A strong influence of the conditioning of chitosan not only on the activity and enantioselectivity but also on the recyclability and reusability of the catalyst is demonstrated. [source] Donor-Stabilized Phosphenium Adducts as New Efficient and Immobilizing Ligands in Palladium-Catalyzed Alkynylation and Platinum-Catalyzed Hydrogenation in Ionic LiquidsADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 10 2009Samer Saleh Abstract The straightforward synthesis of a new donor-stabilized phosphenium ligand 3d by addition of bromodifurylphosphine to 1,3-dimethylimidazolium-2-carboxylate 1 is described. The obtained ligand exhibits a very strong ,-acceptor character, comparable to that of triphenyl phosphite [P(OPh)3] or of tris-halogenophosphines, with a ,CO(A1) at 2087,cm,1 for its nickel tricarbonyl complex. This ligand, as well as the related 3a which was obtained from chlorodiphenylphosphine, were tested in palladium-catalyzed aryl alkynylation and in the platinum-catalyzed selective hydrogenation of chloronitrobenzenes, both in an ionic liquid phase. In CC bond cross-coupling we observed that the increase of the ,-acceptor character in ligand 3d, due to the introduction of an additional electron-withdrawing group, provides a very efficient catalyst in the alkynylation reaction of aryl bromides with phenylacetylene, including the deactivated 4-bromoanisole or the sterically hindered 2-bromonaphthalene. The catalytic activity decreases with recycling due to the sensitiveness of ligands to protonation in the ionic phase. Conversely, a multiple recycling of the metal/ligand system in non-acidic media was achieved from platinum-catalyzed hydrogenation of m- chloronitrobenzene. The catalytic results obtained by employing the complex of platinum(II) chloride with 3a [trans -PtCl2(3a)2] in comparison with the non-ionic related trans -tris(triphenylphosphine)platinum dichloride [trans -PtCl2(PPh3)2] complex clearly indicate that the simultaneous existence of a strong ,-acceptor character and a positive charge within the ligand 3a significantly increases the life-time of the platinum catalyst. The selectivity of the reaction is also improved by decreasing the undesirable formation of dehalogenation products. This cationic platinum complex trans -PtCl2(3a)2 is the first example of a highly selective catalyst for hydrogenation of chloronitroarenes immobilized in an ionic liquid phase. The system was recycled six times without noticeable metal leaching in the organic phase, and no loss of activity. [source] Development of a Supported Ionic Liquid Phase (SILP) Catalyst for Slurry-Phase Friedel,Crafts Alkylations of CumeneADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 3 2009J. Joni Abstract A supported ionic liquid phase (SILP) catalyst material has been developed based on a silica support coated with an acidic chloroaluminate ionic liquid. Compared to the results in a liquid-liquid biphasic reaction these materials showed in the isopropylation of cumene a clearly different selectivity which was found to be related to a reduction of the ionic liquid's acidity by the untreated silica support. By pretreating the support with a defined amount of ionic liquid for neutralization and removal of surface hydroxy groups, a well defined, very active and also very selective SILP catalyst for slurry phase Friedel,Crafts alkylation was obtained. [source] Synthesis of a new photoreactive gelatin with BTDA and HEMA derivativesJOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2008Fan-Chun Ding Abstract A novel bio-affinitive, photocuring, and membrane-forming gelatin derivative was synthesized in this study. This process was based on the amide formation between carboxylic acid and the amine in methanol,water media using dicyclohexyl-carbodiimide (DCC) as a condenser. Gelatin and glycine were the sources of amine in the model reaction. Since there were two anhydride groups in each 3,3,,4,4,-benzophenone tetra-carboxylic dianhydride (BTDA) molecule, two 2-hydroxyethyl methacrylate (HEMA) molecules were used to induce the ring-opening reaction of BTDA and release two carboxylic acid groups. The resulting photoreactive gelatin was called GE-BTHE, of which the photoreactive component was the ketone groups of BTDA and HEMA that played the role of double bond supplier. This photoreactive gelatin could be converted from the transparent liquid phase into swollen membrane by a 6-min irradiation of high pressure mercury lamp. The most efficient irradiation was at 267 nm and the highest degree of swelling of the cured GE-BTHE membrane could reach 5.9. The elongation from the dried gel remained 5,10%, i.e., relatively elastic. The properties of this gelatin derivative were investigated using amide formation analysis, calculation of the gel content and the swelling ratio, and monitoring of the photocuring process. The GE-BTHE synthesized in this study should be very potential in applications such as protective wound dressings and hemostatic absorbents for minimally invasive surgery. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Growth of three bacteria in arsenic solution and their application for arsenic removal from wastewaterJOURNAL OF BASIC MICROBIOLOGY, Issue 6 2008P. Mondal Abstract The present paper compares the arsenic removal capacities of three bacterial strains namely, Ralstonia eutropha MTCC 2487, Pseudomonas putida MTCC 1194 and Bacillus indicus MTCC 4374 form wastewater (simulated acid mine drainage) containing arsenic (As(III):As(V)::1:1), Fe, Mn, Cu and Zn in the concentration of 15 mg/l, 10 mg/l, 2 mg/l, 5 mg/l and 10 mg/l respectively, in bulk liquid phase. Growth patterns of these bacteria in presence of arsenic in solution as well as under starvation have also been investigated as the acid mine drainage normally does not contain organic carbon and also contains high arsenic. At the nutrient broth concentration of 1.25 g/l and in presence of 15 mg/l arsenic sufficient growth of these strains have been observed. However, growth of Ralstonia eutropha MTCC 2487 has been found slightly more than Pseudomonas putida MTCC 1194 and Bacillus indicus MTCC 4374. Arsenic removal capacities of Ralstonia eutropha MTCC 2487, Pseudomonas putida MTCC 1194 and Bacillus indicus MTCC 4374 from simulated acid mine drainage are ,67%, 60% and 61% respectively. It has also been observed that arsenic concentration of 15 mg/l prolongs the stationary phase of these strains. pH and temperature for the above studies have been maintained at 7.1 ± 0.1 and 29 ± 1 °C, respectively. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] The influence of the acidic component of the gas-foaming porogen used in preparing an injectable porous calcium phosphate cement on its properties: Acetic acid versus citric acidJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 1 2008Saeed Hesaraki Abstract In the present study, macroporous calcium phosphate cements (CPCs) were prepared using a porogen; that is, the gas-foaming technique. The objective was to investigate the influence of the acidic component of the porogen (acetic acid versus citric acid) on several properties of a specified CPC. In all of the cements prepared, the basic component of the porogen was the same, namely, NaHCO3, and it was added to the powder phase of the cement, while the acidic component of the porogen was dissolved in the liquid phase of the cement. The cements were characterized in terms of initial setting time, porosity, crystallinity, injectability and compressive strength. Also, XRD, FTIR, and SEM techniques were employed to evaluate the phase composition, the chemical groups and the morphological aspects of the porous cements during setting. It was found that the presence of a porogen in a CPC led to significant decreases in both its initial setting time and compressive strength. A CPC made using acetic acid contained a larger amount of the apatite phase but was significantly less injectable and less porous than when citric acid was used. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2008 [source] | ||||||||||||||||||||||||||||||||||||||||||||||