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The electrocatalytic performance of noble metal nanoparticles depends upon their size, shape, composition, and crystalline facets. Here we demonstrate the shape-dependent electrocatalytic activity of Au nanoparticles toward ascorbic acid oxidation in acidic medium, wherein the catalysis is strongly influenced by the shape of the nanoparticles. The synthesis of (popcorn, tetrapod, and bipod shaped) Au nanoparticles was carried out using a systematic variation of the surfactant concentrations based on the seed-mediated growth technique at room temperature. Due to the facile electrostatic interaction of the positively charged Au nanoparticles with glassy carbon electrode, the modification of the surface with variable-shaped Au nanoparticles is accomplished without involving any binding agents. Among variable-shaped face-centered cubic (fcc) crystalline AuNPs, bipod-shaped Au nanoparticles (GNBipd) exhibit a superior electrocatalytic performance over tetrapod-shaped (GNTepd) and popcorn-shaped (GNPop) nanoparticles as inferred from the differential pulse voltammetry and electrochemical impedance spectroscopy. The results have been explained by invoking the relative surface free energy (?) with preferentially exposed crystal planes, relative surface area (A), zeta potential (?), and the curvature-induced charge density (?q) at the apex for individual variable-shaped gold nanoparticles. � 2015 American Chemical Society.

Mesoporous metals that combine catalytic activity and high surface area can provide more opportunities for electrochemical applications. Various synthetic methods, including hard and soft templating, have been developed to prepare mesoporous/nanoporous metals. Micelle assembly, typically involved in soft-templates, is flexible and convenient for such purposes. It is, however, difficult to control, and the ordering is significantly destroyed during the metal deposition process, which is detrimental when it comes to designing precisely mesostructured materials. In the present work, mesoporous Pd films were uniformly electrodeposited using a nonionic surfactant, triblock copolymer poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide), as a pore-directing agent. The interaction between micelles and metal precursors greatly influences the metal growth and determines the final structure. The water-coordinated species interact with the ethylene oxide moiety of the micelles to effectively drive the Pd(II) species toward the working electrode surface. From small-angle neutron scattering data, it is found that spherical P123 micelles, with an average diameter of ∼14 nm, are formed in the electrolyte, and the addition of Pd ions does not significantly modify their structure, which is the essence of the micelle assembly approach. The uniformly sized mesopores are formed over the entire mesoporous Pd film and have an average pore diameter of 10.9 nm. Cross-sectional observation of the film also shows mesopores spanning continuously from the bottom to the top of the film. The crystallinity, crystal phase, and electronic coordination state of the Pd film are also confirmed. Through this study, it is found that the optimized surfactant concentration and applied deposition potential are the key factors to govern the formation of homogeneous and well-distributed pores over the entire film. Interestingly, the as-prepared mesoporous Pd films exhibit superior electrocatalytic activity toward the ethanol oxidation reaction by fully utilizing the accessible active surface area. Our approach combines electrochemistry with colloidal and coordination chemistry and is widely applicable to other promising metals and alloy electrocatalysts.

Mesoporous TiO2 has been obtained by template synthesis. The introduction of a surfactant in the hydrolysis of tetrabutoxytitanium in aqueous ethanol allows the structure of the resulting material to be controlled. The amorphous TiO2 resulting from hydrolysis turns into anatase on being calcined at 300°C. As determined by X-ray diffraction, the anatase crystallite size is 70 nm in the presence of the highest surfactant concentration examined and 210 nm in the absence of a surfactant. Amorphous materials have been characterized by electron microscopy and differential thermal analysis. The ultimate benzene adsorption value has been determined for calcined mesoporous TiO2. © 2010 Pleiades Publishing, Ltd.

We report here the highly stable niosomes (non-ionic vesicles) from 1:1 Tween-80/Triton X-100 mixed surfactants in presence of n-octanol as an organic additive. Niosomes of nanometer dimensions resulted at a total surfactant concentration ranging from 0.1-1 wt%. The critical concentration of the additive, n-octanol used to form niosomes was found to be 15 mM. The unilamellar vesicles thus formed had a mean diameter of ?100 nm for 0.1 wt% and ?300 nm for 1 wt% concentration. Phase evolution in the mixed 1:1 Tween-80/Triton X-100 surfactant system was unraveled upon investigating the morphology, based on microscopic and dynamic light scattering investigations. The formed vesicles are envisaged as probable potential drug carriers. � (2013) Trans Tech Publications, Switzerland.

The flow of two superposed fluids in a channel in the presence of an insoluble surfactant is studied. Asymptotic analysis when one of the layers is thin yields a system of coupled weakly non-linear evolution equations for the film thickness and the local surface surfactant concentration. Film and main flow dynamics are coupled through a non-local term, and in the absence of surfactants the model is nonlinearly stable with trivial large time solutions. Instability arises due to the presence of surfactants and the pseudo-differential non-linear system is solved numerically by implementing accurate linearly implicit methods. Extensive numerical experiments reveal that the dynamics are mostly organized into travelling or time-periodic travelling wave pulses, but spatiotemporal chaos is also supported when the length of the system is sufficiently large. © The authors 2012. 77 3 351 360 Cited By :3

Bubbles bursting from whitecaps are considered to be the most effective mechanism for particulate matter to be ejected into the atmosphere from the Earth's oceans. To realistically predict the climate effect of marine aerosols, global climate models require process-based understanding of particle formation from bubble bursting. During a cruise on the highly biologically active waters of the northeastern Atlantic Ocean in the summer of 2006, the submicrometer primary marine aerosol produced by a jet of seawater impinging on a seawater surface was investigated. The produced aerosol size spectra were centered on 200 nm in dry diameter and were conservative in shape throughout the cruise. The aerosol number production was negatively correlated with dissolved oxygen (DO) in the water (r < -0.6 for particles of dry diameter Dp > 200 nm). An increased surfactant concentration as a result of biological activity affecting the oxygen saturation is thought to diminish the particle production. The lack of influence of chlorophyll on aerosol production indicates that hydrocarbons produced directly by the photosynthesis are not essential for sea spray production. The upward mixing of deeper ocean water as a result of higher wind speed appears to affect the aerosol particle production, making wind speed influence aerosol production in more ways than by increasing the amount of whitecaps. The bubble spectra produced by the jet of seawater was representative of breaking waves at open sea, and the particle number production was positively correlated with increasing bubble number concentration with a peak production of 40-50 particles per bubble. Copyright 2010 by the American Geophysical Union.

Selection of the surfactant has an impact on many of the foam properties as it affects the surface tension and gas-liquid interfacial properties. The objective is to produce stable aqueous foam of required density. These two characteristics are influenced by the type of surfactant, its concentration and foam generation pressure. This study compares the density and stability of foam produced using four synthetic surfactants namely sodium lauryl sulfate, sodium lauryl ether sulfate, sulfanol and cocodiethanolamide through a systematic experiment design based on response surface methodology. The relative performance has also been assessed in terms of their suitability for use in foamed concrete production based on ASTM test method. The effect of surfactant concentration has relatively lesser effect on foam density for sodium lauryl sulfate and sulfanol irrespective of foam generation pressure adopted. The drainage is proportional to the initial foam density for all the surfactant concentration for ionic surfactants at different foam generation pressures. For all the four surfactants under the optimum foam generation pressure, a stable foam with drainage less than 12% in 300 s (by considering economy as a factor) is achieved. From the foam stability test based on ASTM C 796-97, it is observed that all the four surfactants are suitable for use in foamed concrete production when optimized foam production parameters are adopted. � 2010 RILEM.

Bubbles bursting from whitecaps are considered to be the most effective mechanism for particulate matter to be ejected into the atmosphere from the Earth's oceans. To realistically predict the climate effect of marine aerosols, global climate models require process-based understanding of particle formation from bubble bursting. During a cruise on the highly biologically active waters of the northeastern Atlantic Ocean in the summer of 2006, the submicrometer primary marine aerosol produced by a jet of seawater impinging on a seawater surface was investigated. The produced aerosol size spectra were centered on 200 nm in dry diameter and were conservative in shape throughout the cruise. The aerosol number production was negatively correlated with dissolved oxygen (DO) in the water (r < -0.6 for particles of dry diameter Dp > 200 nm). An increased surfactant concentration as a result of biological activity affecting the oxygen saturation is thought to diminish the particle production. The lack of influence of chlorophyll on aerosol production indicates that hydrocarbons produced directly by the photosynthesis are not essential for sea spray production. The upward mixing of deeper ocean water as a result of higher wind speed appears to affect the aerosol particle production, making wind speed influence aerosol production in more ways than by increasing the amount of whitecaps. The bubble spectra produced by the jet of seawater was representative of breaking waves at open sea, and the particle number production was positively correlated with increasing bubble number concentration with a peak production of 40-50 particles per bubble. Copyright 2010 by the American Geophysical Union.

The effect of surfactants sodium dodecyl sulphate (SDS) and cetyltrimethyl ammonium bromide (CTAB) on the surface roughness, surface morphology and surface topography of electroless nickel (EN)-phosphorus surface protective coating obtained from an alkaline bath is presented in this paper. In this study the influence of surfactant concentrations on the surface roughness of coated samples were investigated. It was observed that the surface roughness, surface morphology and surface topography of Ni-P coating were clearly influenced by the addition of surfactants SDS and CTAB. EN deposits with addition of surfactant SDS and CTAB at a concentration of 0.6 g/l produce a smooth surface and the average roughness (Ra) value is 1.715 ?m for SDS and 1.607 ?m for CTAB which is less than the Ra value of EN deposit without surfactant addition (1.885 ?m). The mean average roughness (Ra) value with addition of surfactant is 1.796 ?m. EN deposit with addition of surfactants consists of a significant fraction of particles of nickel. In the presence of SDS, fine nickel particles have dispersed uniformly on the substrate surface resulting in smoother surface finish of the deposited layers. In the presence of CTAB, at lower concentrations (upto 0.6 g/l) coalescence of nickel particles have been deposited on the substrate surface and at the higher concentration (above 0.6 g/l) uniformly improved surface finish of the deposited layer is resulted. The complete experimental details, results obtained and their analysis are presented in this paper. � 2008 Elsevier B.V. All rights reserved.

5 pages, 10 figures, 1 table.-- Printed version published Sep 2, 2003., Oil/water (O/W) nano-emulsions have been formed in the system water/C16E6/mineral oil by the phase inversion temperature (PIT) method. The relation between the phase equilibria observed at the hydrophilic−lipophilic balance (HLB) temperature or the PIT (i.e., the nature, number, and relative volume fractions of the involved phases), the droplet sizes, and polydispersities of the resulting emulsions have been determined. Milky white emulsions were obtained when, at the HLB temperature, a three-phase equilibrium formed by water (W), shear-birefringent microemulsion (D), and oil (O) was observed. However, bluish transparent O/W nano-emulsions with droplet sizes as low as 40 nm were formed in a narrow range of oil-to-surfactant ratios in which a D or W + D phases were the initial equilibrium phases. In the W + D equilibria, droplet sizes were independent from the water content, indicating that nanodroplet formation is mainly controlled by the structure of the D phase. These results suggest that the main requirement for bluish transparent O/W nano-emulsion formation is the complete solubilization of the oil component in a bicontinuous microemulsion, independent of whether the initial phase equilibrium is single or multiphase., Financial support from MCYT (Grant PPQ2002-04514-CO3), and from the Generalitat de Catalunya DURSI (Grant 2001SGR-00357).