Surface activity and fluorite flotation with myristic acid derivatives containing oxygen and sulphur atoms

Surface tension isotherms and fluorite flotation were studied in systems containing myristic acid derivatives in which carbon atoms in the hydrocarbon skeleton were partly replaced by oxygen and/or sulphur atoms. The location of the oxygen and sulphur atoms affects significantly compound hydrophobicity, adsorption at the air/water interface and fluorite flotation. The most effective collectors were the compounds with one oxygen or sulphur atom close to the carboxylic group.     

Diffusive dynamics of water in tert-butyl alcohol/water mixtures

Quasielastic neutron scattering has been used to investigate the dynamical behavior of H(2)O in water/tert-butyl alcohol solutions. The measurements were made at fixed temperature (293 K) as a function of tert-butyl alcohol molar fraction, x, in the range 0-0.042. The data have been compared to those of pure water in the temperature range 269-293 K. The effect of tert-butyl alcohol addition on water dynamics is equivalent to that obtained by lowering the temperature of pure water by an amount proportional to the alcohol concentration. The temperature dependence of the diffusivity parameters in pure water and their concentration dependence in tert-butyl alcohol/water solutions can be rescaled to a common curve attributing to each solution a concentration-dependent "structural temperature" lower than the actual thermodynamic one. These results can be understood in terms of Stillinger's picture of water structuring and of other more recent theoretical pictures that emphasize the influence of the geometrical properties of hydrogen bond networks on water mobility.     

(Eco)toxicity of fluoro-organic and cyano-based ionic liquid anions

The (eco)toxicity of the most common ionic liquid anions like [N(CN)(2)](-), [C(CN)(3)](-), [B(CN)(4)](-), [(CF(3)SO(2))(2)N](-), [(C(2)F(5))(3)PF(3)](-) was investigated in test systems of different trophic level. In the same order, and thus with increasing hydrophobicity, a trend of higher toxicity was found. Especially the [(C(2)F(5))(3)PF(3)](-) moiety poses a significant hazard towards aquatic organisms.     

Two-site adsorption model for the (square root 3 x square root 3)-R30 degrees dodecanethiolate lattice on Au(111) surfaces

The surface structure of dodecanethiolate self-assembled monolayers (SAMs) on Au(111) surfaces, formed from the liquid phase, have been studied by grazing incidence X-ray diffraction (GIXRD), scanning tunneling microscopy (STM), and electrochemical techniques. STM images show that the surface structure consists of (square root 3 x square root 3)-R30 degrees domains with only a few domains of the c(4 x 2) lattice. The best fitting of GIXRD data for the (square root 3 x square root 3)-R30 degrees lattice is obtained with alkanethiolate adsorption at the top sites, although good fittings are also obtained for the fcc and hcp hollow sites. On the basis of this observation, STM data, electrochemical measurements, and previously reported data, we propose a two-site model that implies the formation of incoherent domains of alkanethiolate molecules at top and fcc hollow sites. This model largely improves the fitting of the GIXRD data with respect to those observed for single adsorption sites and, also, for the other possible two-site combinations. The presence of alkanethiolate molecules adsorbed at the less favorable top sites could result from the adsorption pathway that involves an initial physisorption step which, for steric reasons, takes place at on top sites. Once the molecules are chemisorbed, the presence of energy barriers for alkanethiolate surface diffusion, arising mostly from chain-chain interactions, "freezes" some of them at the on top sites, hindering their movement toward fcc hollow sites. By considering the length of the hydrocarbon chain and the adsorption time, the two-site model could be a tool to explain most of the controversial results on this matter reported in the literature.     

Carbon monoxide adsorption on silver doped gold clusters

Well controlled gas phase experiments of the size and dopant dependent reactivity of gold clusters can shed light on the surprising discovery that nanometer sized gold particles are catalytically active. Most studies that investigate the reactivity of gold clusters in the gas phase focused on charged, small sized clusters. Here, reactivity measurements in a low-pressure reaction cell were performed to investigate carbon monoxide adsorption on neutral bare and silver doped gold clusters (Au(n)Ag(m); n = 10-45; m = 0, 1, 2) at 140 K. The size dependence of the reaction probabilities reflects the role of the electronic shells for the carbon monoxide adsorption, with closed electronic shell systems being the most reactive. In addition, the cluster's reaction probability is reduced upon substitution of gold atoms for silver. Inclusion of a single silver atom causes significant changes in the reactivity only for a few cluster sizes, whereas there is a more general reduction in the reactivity with two silver atoms in the cluster. The experimental observations are qualitatively explained on the basis of a Blyholder model, which includes dopant induced features such as electron transfer from silver to gold, reduced s-d hybrization, and changes in the cluster geometry.     

Influence of the Hofmeister anions on self-organization of 1-decyl-3-methylimidazolium chloride in aqueous solutions

Inorganic salts usually influence water structure affecting the hydration of the molecules which lead to a salting-in or a salting-out effect of hydrophobic compounds. Specific conductivity and isothermal titration calorimetry have been used to study the effect of inorganic salts on aggregation of the cationic surfactant 1-decyl-3-methylimidazolium chloride in aqueous solutions. The effect of the concentration, the nature of the anion and temperature on micelle formation were studied. A decreasing critical micelle concentration (CMC) due to the weakening electrostatic repulsion between the headgroups was observed. The salts used in this investigation decreased the CMC and degree of micelle ionization in the order of Cl(-)相似文献   

Growth Mechanism and Chemical Bonding in Scandium‐Doped Copper Clusters: Experimental and Theoretical Study in Concert

Size matters! The electronic structure and size‐dependent stability of neutral and cationic scandium‐doped copper clusters have been investigated by mass spectrometric studies (for the cations) and also quantum chemical computations. The proposed reaction paths ultimately lead to the most stable Frank–Kasper‐shaped Cu₁₆Sc⁺ cluster (shown here), which could be the germ of a new crystallization process.

     

ChemInform Abstract: Experimental Detection and Theoretical Characterization of Germanium‐Doped Lithium Clusters LinGe (n = 1—7).

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.     

Electrodeless dielectrophoresis: Impact of geometry and material on obstacle polarization

Insulator‐based (electrodeless) dielectrophoresis (iDEP) is a promising particle manipulation technique, based on movement of matter in inhomogeneous fields. The inhomogeneity of the field arises because the excitatory field distorts at obstacles (posts). This effect is caused by accumulation of polarization charges at material interfaces. In this study, we utilize a multipole expansion method to investigate the influence of geometry and material on field distortion of posts with arbitrary cross‐sections in homogeneous electric fields applied perpendicular to the longitudinal axis of the post. The post then develops a multipole parallel or anti parallel to the excitatory field. The multipoles intensity is defined by the post's structure and material properties and directly influences the DEP particle trapping potential. We analyzed posts with circular and rhombus‐shaped cross‐sections with different cross‐sectional width‐to‐height ratios and permittivities for their polarization intensity, multipole position, and their particle trapping behavior. A trade‐off between high maximum field gradient and high coverage range of the gradient is presented, which is determined by the sharpness of the post's edges. We contribute to the overall understanding of the post polarization mechanism and expect that the results presented will help optimizing the structure of microchannels with arrays of posts for electrodeless DEP application.     

Development of an analytical method for antimony speciation in vegetables by HPLC-hydride generation-atomic fluorescence spectrometry

A new method for antimony speciation in terrestrial edible vegetables (spinach, onions, and carrots) was developed using HPLC with hydride generation-atomic fluorescence spectrometry. Mechanical agitation and ultrasound were tested as extraction techniques. Different extraction reagents were evaluated and optimal conditions were determined using experimental design methodology, where EDTA (10 mmol/L, pH 2.5) was selected because this chelate solution produced the highest extraction yield and exhibited the best compatibility with the mobile phase. The results demonstrated that EDTA prevents oxidation of Sb(III) to Sb(V) and maintains the stability of antimony species during the entire analytical process. The LOD and precision (RSD values obtained) for Sb(V), Sb(III), and trimethyl Sb(V) were 0.08, 0.07, and 0.9 microg/L and 5.0, 5.2, and 4.7%, respectively, for a 100 microL sample volume. The application of this method to real samples allowed extraction of 50% of total antimony content from spinach, while antimony extracted from carrots and onion samples ranged between 50 and 60 and 54 and 70%, respectively. Only Sb(V) was detected in three roots (onion and spinach) that represented 60-70% of the total antimony in the extracts.