Showing papers on "Particle published in 2006"

Silver Colloid Nanoparticles: Synthesis, Characterization, and Their Antibacterial Activity

Abstract: A one-step simple synthesis of silver colloid nanoparticles with controllable sizes is presented. In this synthesis, reduction of [Ag(NH3)2]+ complex cation by four saccharides was performed. Four saccharides were used: two monosaccharides (glucose and galactose) and two disaccharides (maltose and lactose). The syntheses performed at various ammonia concentrations (0.005−0.20 mol L-1) and pH conditions (11.5−13.0) produced a wide range of particle sizes (25−450 nm) with narrow size distributions, especially at the lowest ammonia concentrations. The average size, size distribution, morphology, and structure of particles were determined by dynamic light scattering (DLS), transmission electron microscopy (TEM), and UV/Visible absorption spectrophotometry. The influence of the saccharide structure (monosacharides versus disaccharides) on the size of silver particles is briefly discussed. The reduction of [Ag(NH3)2]+ by maltose produced silver particles with a narrow size distribution with an average size of ...

Tailoring Surface Plasmons through the Morphology and Assembly of Metal Nanoparticles

Abstract: Metal nanoparticles can be used as building blocks for the formation of nanostructured materials. For the design of materials with specific (optical) properties, several approaches can be followed, even when starting from the very same basic units. In this article, a survey is provided of the optical properties of noble metal nanoparticles, specifically gold, silver, and their combinations, prepared in solution through colloid chemical methods. The optical properties are shown to be mainly influenced by the surface plasmon resonance of conduction electrons, the frequency of which is not only determined by the nature of the metal but also by a number of other parameters, such as particle size and shape, the presence of a capping shell on the particle surface, or the dielectric properties of the surrounding medium. Recent results showing how these various parameters affect the optical properties are reviewed. The results highlight the high degree of control that can now be achieved through colloid chemical synthesis.

Kinetically driven self assembly of highly ordered nanoparticle monolayers

Abstract: When a drop of a colloidal solution of nanoparticles dries on a surface, it leaves behind coffee-stain-like rings of material with lace-like patterns or clumps of particles in the interior. These non-uniform mass distributions are manifestations of far-from-equilibrium effects, such as fluid flows and solvent fluctuations during late-stage drying. However, recently a strikingly different drying regime promising highly uniform, long-range-ordered nanocrystal monolayers has been found. Here we make direct, real-time and real-space observations of nanocrystal self-assembly to reveal the mechanism. We show how the morphology of drop-deposited nanoparticle films is controlled by evaporation kinetics and particle interactions with the liquid-air interface. In the presence of an attractive particle-interface interaction, rapid early-stage evaporation dynamically produces a two-dimensional solution of nanoparticles at the liquid-air interface, from which nanoparticle islands nucleate and grow. This self-assembly mechanism produces monolayers with exceptional long-range ordering that are compact over macroscopic areas, despite the far-from-equilibrium evaporation process. This new drop-drying regime is simple, robust and scalable, is insensitive to the substrate material and topography, and has a strong preference for forming monolayer films. As such, it stands out as an excellent candidate for the fabrication of technologically important ultra thin film materials for sensors, optical devices and magnetic storage media.

Continuous-flow lithography for high-throughput microparticle synthesis

Abstract: Precisely shaped polymeric particles and structures are widely used for applications in photonic materials, MEMS, biomaterials and self-assembly. Current approaches for particle synthesis are either batch processes or flow-through microfluidic schemes that are based on two-phase systems, limiting the throughput, shape and functionality of the particles. We report a one-phase method that combines the advantages of microscope projection photolithography and microfluidics to continuously form morphologically complex or multifunctional particles down to the colloidal length scale. Exploiting the inhibition of free-radical polymerization near PDMS surfaces, we are able to repeatedly pattern and flow rows of particles in less than 0.1 s, affording a throughput of near 100 particles per second using the simplest of device designs. Polymerization was also carried out across laminar, co-flowing streams to generate Janus particles containing different chemistries, whose relative proportions could be easily tuned. This new high-throughput technique offers unprecedented control over particle size, shape and anisotropy.

Electrodeposition of composite coatings containing nanoparticles in a metal deposit

Abstract: Recent literature on the electrodeposition of metallic coatings containing nanosized particles is surveyed. The nanosized particles, suspended in the electrolyte by agitation and/or use of surfactants, can be codeposited with the metal. The inclusion of nanosized particles can give (i) an increased microhardness and corrosion resistance, (ii) modified growth to form a nanocrystalline metal deposit and (iii) a shift in the reduction potential of a metal ion. Many operating parameters influence the quantity of incorporated particles, including current density, bath agitation (or movement of work piece) and electrolyte composition. High incorporation rates of the dispersed particles have been achieved using (i) a high nanoparticle concentration in the electrolyte solution, (ii) smaller sized nanoparticles; (iii) a low concentration of electroactive species, (iv) ultrasonication during deposition and (v) pulsed current techniques. Compositional gradient coatings are possible having a controlled distribution of particles in the metal deposit and the theoretical models used to describe the phenomenon of particle codeposition within a metal deposit are critically considered.

Two-Dimensional Nematic Colloidal Crystals Self-Assembled by Topological Defects

Abstract: The ability to generate regular spatial arrangements of particles is an important technological and fundamental aspect of colloidal science We showed that colloidal particles confined to a few-micrometer-thick layer of a nematic liquid crystal form two-dimensional crystal structures that are bound by topological defects Two basic crystalline structures were observed, depending on the ordering of the liquid crystal around the particle Colloids inducing quadrupolar order crystallize into weakly bound two-dimensional ordered structure, where the particle interaction is mediated by the sharing of localized topological defects Colloids inducing dipolar order are strongly bound into antiferroelectric-like two-dimensional crystallites of dipolar colloidal chains Self-assembly by topological defects could be applied to other systems with similar symmetry

Control of colloidal particle deposit patterns within picoliter droplets ejected by ink-jet printing.

Abstract: Particle deposit morphologies that resulted from evaporating ink-jetted microdroplets were controlled by varying the ink compositions and concentrations. The ink was a well-dispersed aqueous dispersion of monodisperse silica microspheres. Silica particles suspended in the microdroplet undergo self-assembly upon the evaporation of the solvent. A ringlike deposit of the self-assembled silica particles was produced from the water-based ink, while a uniform two-dimensional monolayer with a well-ordered hexagonal structure was obtained from the mixed-solvent-based inks. Variations in the deposit patterns can be explained in terms of competing effects between the convective and Marangoni flows, which vary with the types of the high-boiling-point solvent added to the ink. The macroscopic shape and microstructure of the silica colloidal deposits were observed by SEM, AFM, and a confocal microscope.

Single‐particle measurements of midlatitude black carbon and light‐scattering aerosols from the boundary layer to the lower stratosphere

Abstract: A single-particle soot photometer (SP2) was flown on a NASA WB-57F high-altitude research aircraft in November 2004 from Houston, Texas. The SP2 uses laser-induced incandescence to detect individual black carbon (BC) particles in an air sample in the mass range of $3-300 fg ($0.15-0.7 mm volume equivalent diameter). Scattered light is used to size the remaining non-BC aerosols in the range of $0.17-0.7 mm diameter. We present profiles of both aerosol types from the boundary layer to the lower stratosphere from two midlatitude flights. Results for total aerosol amounts in the size range detected by the SP2 are in good agreement with typical particle spectrometer measurements in the same region. All ambient incandescing particles were identified as BC because their incandescence properties matched those of laboratory-generated BC aerosol. Approximately 40% of these BC particles showed evidence of internal mixing (e.g., coating). Throughout profiles between 5 and 18.7 km, BC particles were less than a few percent of total aerosol number, and black carbon aerosol (BCA) mass mixing ratio showed a constant gradient with altitude above 5 km. SP2 data was compared to results from the ECHAM4/MADE and LmDzT-INCA global aerosol models. The comparison will help resolve the important systematic differences in model aerosol processes that determine BCA loadings. Further intercomparisons of models and measurements as presented here will improve the accuracy of the radiative forcing contribution from BCA.

Rapid Production of Metal−Organic Frameworks via Microwave-Assisted Solvothermal Synthesis

Abstract: This paper describes a very rapid technique for the production of metal−organic frameworks (MOF). The method uses a conventional microwave to nucleate crystal growth. A MOF synthesis that used to take hours or days can now be completed in 30 s to 2 min. The yield goes from ∼30% to over 90%. Novel MOFs can be made, since the growth process is no longer dependent on the walls or dust particles for nucleation. Particle sizes have a narrower distribution. Further, the particle size can be controlled by varying the precursor concentration.

Colloidal Particles at Liquid Interfaces

Abstract: 1. Particles at liquid interfaces - an introduction B. P. Binks and T. S. Horozov 2. Structure and formation of particle monolayers at liquid interfaces L. Bergstrom 3. Theory for interactions between particles in monolayers J. C. Fernandez-Toledano, A. Moncho-Jorda, F. Martinez-Lopez and R. Hidalgo-Alvarez 4. Particle-assisted wetting W. A. Goedel 5. Particle-laden interfaces: rheology, coalescence, adhesion and buckling G. G. Fuller, E. J. Stancik and S. Melle 6. Solids-stabilized emulsions: a review R. J. G. Lopetinksy, J. H. Masliyah and Z. Xu 7. Novel materials derived from particles assembled on liquid surfaces K. P. Velikov and O. D. Velev 8. Interfacial particles in food emulsions and foams E. Dickinson 9. Collection and attachment of particles by air bubbles in froth flotation A. V. Nguyen, R. J. Pugh and G. J. Jameson 10. Antifoam effects of solid particles, oil drops and oil-solid compounds in aqueous foams N. D. Denkov and K. G. Marinova 11. Metal foams: towards high temperature colloid chemistry N. Babcsan and J. Banhart.

Stress generation and fracture in lithium insertion materials

Abstract: A mathematical model that calculates volume expansion and contraction and concentration and stress profiles during lithium insertion into and extraction from a spherical particle of electrode material has been developed. The maximum stress in the particle has been determined as a function of dimensionless current, which includes the charge rate, particle size, and diffusion coefficient. The effects of pressure-driven diffusion and nonideal interactions between the lithium and host material have also been described. The model predicts that carbonaceous particles will fracture in high-power applications such as hybrid-electric vehicle batteries.

Ultrastable Particle‐Stabilized Foams

Abstract: Pump up the volume: Wet foams prepared with surfactants are thermodynamically unstable systems that undergo rapid disproportionation, drainage, and coalescence. Ultrastable foams have now been prepared using colloidal particles as stabilizers (left picture). The stabilization results from the irreversible adsorption at the air–water interface of particles surface-modified with short-chain amphiphiles (right picture).

Phase inversion of particle-stabilized materials from foams to dry water.

Abstract: Small particles attached to liquid surfaces arise in many products and processes, including crude-oil emulsions and food foams and in flotation, and there is a revival of interest in studying their behaviour. Colloidal particles of suitable wettability adsorb strongly to liquid-liquid and liquid-vapour interfaces, and can be sole stabilizers of emulsions and foams, respectively. New materials, including colloidosomes, anisotropic particles and porous solids, have been prepared by assembling particles at such interfaces. Phase inversion of particle-stabilized emulsions from oil in water to water in oil can be achieved either by variation of the particle hydrophobicity (transitional) or by variation of the oil/water ratio (catastrophic). Here we describe the phase inversion of particle-stabilized air-water systems, from air-in-water foams to water-in-air powders and vice versa. This inversion can be driven either by a progressive change in silica-particle hydrophobicity at constant air/water ratio or by changing the air/water ratio at fixed particle wettability, and has not been observed in the corresponding systems stabilized by surfactants. The simplicity of the work is that this novel inversion is achieved in a single system. The resultant materials in which either air or water become encapsulated have potential applications in the food, pharmaceutical and cosmetics industries.

Limitations in the enhancement of visible light absorption due to mixing state

Abstract: [1] Absorption by light-absorbing carbon (LAC) particles increases when the carbon is mixed with other material, and this change affects climate forcing. We investigate this increase theoretically over a realistic range of particle sizes. Perfect mixing at the molecular level often overestimates absorption. Assuming that LAC is coated by a concentric shell of weakly absorbing material, we calculate absorption by a range of realistic particle sizes and identify regimes in which absorption behaves similarly. We provide fits to amplification in five regions: (1) small cores and (2) intermediate cores, both with large shells; (3) small to intermediate cores with intermediate shells; (4) cores with growing shells; and (5) intermediate to large cores with large shells. Amplification in region 1 is highest but is physically implausible. Amplification in region 5 is constant at about 1.9 and represents an asymptote for particles with broad size distributions. Because absorption by aggregates is amplified by about 1.3 above spherical particles, and that factor is lost when particles are coated, we suggest that absorption by aged aerosol is about 1.5 times greater than that of fresh aerosol. The rate at which particles acquire sufficient coating to increase their original diameter by 60% is important in determining total absorption during their atmospheric lifetimes. Fitted amplification factors are not very sensitive to assumed refractive index of LAC and can be used even in simple models.

Influence of surface potential on aggregation and transport of titania nanoparticles.

Abstract: To investigate the effect of pH on nanoparticle aggregation and transport in porous media, we quantified nanoparticle transport in two-dimensional structures. Titania was used as a model compound to explore the effects of surface potential on particle mobility in the subsurface. Results show that pH, and therefore, surface potential and aggregate size, dominate nanoparticle interactions with each other and surfaces. In each solution, nanoparticle aggregate size distributions were bimodal or trimodal, and aggregate sizes increased as the pH approached the pH of the point of zero charge (pHzpc). Over 80% of suspended particles and aggregates were mobile over the pH range of 1−12, except close to the pHzpc of the surfaces, where the particles are highly aggregated. The effect of pH on transport is not symmetric around the pHzpc of the particles due to charging of the channel surfaces. However, transport speed of nanoparticle aggregates did not vary with pH. The surface element integration technique, which ta...

Direct laser sintering of metal powders: Mechanism, kinetics and microstructural features

Abstract: In the present work, the densification and microstructural evolution during direct laser sintering of metal powders were studied. Various ferrous powders including Fe, Fe–C, Fe–Cu, Fe–C–Cu–P, 316L stainless steel, and M2 high-speed steel were used. The empirical sintering rate data was related to the energy input of the laser beam according to the first order kinetics equation to establish a simple sintering model. The equation calculates the densification of metal powders during direct laser sintering process as a function of operating parameters including laser power, scan rate, layer thickness and scan line spacing. It was found that when melting/solidification approach is the mechanism of sintering, the densification of metals powders ( D ) can be expressed as an exponential function of laser specific energy input ( ψ ) as ln(1 − D ) = − Kψ . The coefficient K is designated as “densification coefficient”; a material dependent parameter that varies with chemical composition, powder particle size, and oxygen content of the powder material. The mechanism of particle bonding and microstructural features of the laser sintered powders are addressed.

Polymer hollow particles with controllable holes in their surfaces

Abstract: A hollow polymer particle having a single, substantially circular opening in the particle's surface, methods for making and using the polymer particle.

Atmospheric sulphuric acid and aerosol formation: implications from atmospheric measurements for nucleation and early growth mechanisms

Abstract: . We have investigated the formation and early growth of atmospheric secondary aerosol particles building on atmospheric measurements. The measurements were part of the QUEST 2 campaign which took place in spring 2003 in Hyytiala (Finland). During the campaign numerous aerosol particle formation events occurred of which 15 were accompanied by gaseous sulphuric acid measurements. Our detailed analysis of these 15 events is focussed on nucleation and early growth (to a diameter of 3 nm) of fresh particles. It revealed that new particle formation seems to be a function of the gaseous sulphuric acid concentration to the power from one to two when the time delay between the sulphuric acid and particle number concentration is taken into account. From the time delay the growth rates of freshly nucleated particles from 1 nm to 3 nm were determined. The mean growth rate was 1.2 nm/h and it was clearly correlated with the gaseous sulphuric acid concentration. We tested two nucleation mechanisms – recently proposed cluster activation and kinetic type nucleation – as possible candidates to explain the observed dependences, and determined experimental nucleation coefficients. We found that some events are dominated by the activation mechanism and some by the kinetic mechanism. Inferred coefficients for the two nucleation mechanisms are the same order of magnitude as chemical reaction coefficients in the gas phase and they correlate with the product of gaseous sulphuric acid and ammonia concentrations. This indicates that besides gaseous sulphuric acid also ammonia has a role in nucleation.

Fabrication of Hollow Inorganic Microspheres by Chemically Induced Self‐Transformation

Abstract: Two contrasting approaches, involving either polymer-mediated or fluoride-mediated self-transformation of amorphous solid particles, are described as general routes to the fabrication of hollow inorganic microspheres. Firstly, calcium carbonate and strontium tungstate hollow microspheres are fabricated in high yield using sodium poly(4-styrenesulfonate) as a stabilizing agent for the formation and subsequent transformation of amorphous primary particles. Transformation occurs with retention of the bulk morphology by localized Ostwald ripening, in which preferential dissolution of the particle interior is coupled to the deposition of a porous external shell of loosely packed nanocrystals. Secondly, the fabrication process is extended to relatively stable amorphous microspheres, such as TiO2 and SnO2, by increasing the surface reactivity of the solid precursor particles. For this, fluoride ions, in the form of NH4F and SnF2, are used to produce well-defined hollow spheroids of nanocrystalline TiO2 and SnO2, respectively. Our results suggest that the chemical self-transformation of precursor objects under morphologically invariant conditions could be of general applicability in the preparation of a wide range of nanoparticle-based hollow architectures for technological and biomedical applications.

Drug nanoparticles by antisolvent precipitation: mixing energy versus surfactant stabilization.

Abstract: Organic itraconazole (ITZ) solutions were mixed with aqueous solutions to precipitate sub-300 nm particles over a wide range of energy dissipation rates, even for drug loadings as high as 86% (ITZ weight/total weight). The small particle sizes were produced with the stabilizer poloxamer 407, which lowered the interfacial tension, increasing the nucleation rate while inhibiting growth by coagulation and condensation. The highest nucleation rates and slowest growth rates were found at temperatures below 20 degrees C and increased with surfactant concentration and Reynolds number (Re). This increase in the time scale for growth reduced the Damkohler number (Da) (mixing time/precipitation time) to low values even for modest mixing energies. As the stabilizer concentration increased, the average particle size decreased and reached a threshold where Da may be considered to be unity. Da was maintained at a low value by compensating for a change in one variable away from optimum conditions (for small particles) by manipulating another variable. This tradeoff in compensation variables was demonstrated for organic flow rate vs Re, Re vs stabilizer concentration, stabilizer feed location (organic phase vs aqueous phase) vs stabilizer concentration, and stabilizer feed location vs Re. A decrease in the nucleation rate with particle density in the aqueous suspension indicated that secondary nucleation was minimal. A fundamental understanding of particle size control in antisolvent precipitation is beneficial for designing mixing systems and surfactant stabilizers for forming nanoparticles of poorly water soluble drugs with the potential for high dissolution rates.

Organic C and N stabilization in a forest soil: Evidence from sequential density fractionation

Abstract: In mineral soil, organic matter (OM) accumulates mainly on and around surfaces of silt- and clay-size particles. When fractionated according to particle density, C and N concentration (per g fraction) and C/N of these soil organo-mineral particles decrease with increasing particle density across soils of widely divergent texture, mineralogy, location, and management. The variation in particle density is explained potentially by two factors: (1) a decrease in the mass ratio of organic to mineral phase of these particles, and (2) variations in density of the mineral phase. The first explanation implies that the thickness of the organic accumulations decreases with increasing particle density. The decrease in C/N can be explained at least partially by especially stable sorption of nitrogenous N-containing compounds (amine, amide, and pyrrole) directly to mineral surfaces, a phenomenon well documented both empirically and theoretically. These peptidic compounds, along with ligand-exchanged carboxylic compounds, could then form a stable inner organic layer onto which other organics could sorb more readily than onto the unconditioned mineral surfaces (“onion” layering model). To explore mechanisms underlying this trend in C concentration and C/N with particle density, we sequentially density fractionated an Oregon andic soil at 1.65, 1.85, 2.00, 2.28, and 2.55 g cm −3 and analyzed the six fractions for measures of organic matter and mineral phase properties. All measures of OM composition showed either: (1) a monotonic change with density, or (2) a monotonic change across the lightest fractions, then little change over the heaviest fractions. Total C, N, and lignin phenol concentration all decreased monotonically with increasing density, and 14 C mean residence time (MRT) increased with particle density from ca. 150 years to >980 years in the four organo-mineral fractions. In contrast, C/N, 13 C and 15 N concentration all showed the second pattern. All these data are consistent with a general pattern of an increase in extent of microbial processing with increasing organo-mineral particle density, and also with an “onion” layering model. X-ray diffraction before and after separation of magnetic materials showed that the sequential density fractionation (SDF) isolated pools of differing mineralogy, with layer-silicate clays dominating in two of the intermediate fractions and primary minerals in the heaviest two fractions. There was no indication that these differences in mineralogy controlled the differences in density of the organo-mineral particles in this soil. Thus, our data are consistent with the hypothesis that variation in particle density reflects variation in thickness of the organic accumulations and with an “onion” layering model for organic matter accumulation on mineral surfaces. However, the mineralogy differences among fractions made it difficult to test either the layer-thickness or “onion” layering models with this soil. Although SDF isolated pools of distinct mineralogy and organic-matter composition, more work will be needed to understand mechanisms relating the two factors.

The contribution of boundary layer nucleation events to total particle concentrations on regional and global scales

Abstract: The contribution of boundary layer nucleation events to total particle concentrations on the global scale has been studied by including a new particle formation mechanism in a global aerosol microphysics model. The mechanism is based on an analysis of extensive observations of particle formation in the boundary layer at a continental surface site. It assumes that molecular clusters form at a rate proportional to the gaseous sulfuric acid concentration to the power of 1. The formation rate of 3 nm diameter observable particles is controlled by the cluster formation rate and the existing particle surface area, which acts to scavenge condensable gases and clusters during growth. Modelled sulfuric acid vapour concentrations, particle formation rates, growth rates, coagulation loss rates, peak particle concentrations, and the daily timing of events in the global model agree well with observations made during a 22-day period of March 2003 at the SMEAR II station in Hyytiala, Finland. The nucleation bursts produce total particle concentrations (>3 nm diameter) often exceeding 104 cm?3, which are sustained for a period of several hours around local midday. The predicted global distribution of particle formation events broadly agrees with what is expected from available observations. Over relatively clean remote continental locations formation events can sustain mean total particle concentrations up to a factor of 8 greater than those resulting from anthropogenic sources of primary organic and black carbon particles. However, in polluted continental regions anthropogenic primary particles dominate particle number and formation events lead to smaller enhancements of up to a factor of 2. Our results therefore suggest that particle concentrations in remote continental are dominated by nucleated particles while concentrations in polluted continental regions are dominated by primary particles. The effect of boundary layer particle formation over tropical regions and the Amazon is negligible. Particle concentrations are enhanced by a factor 3?10 over the remote Southern Ocean (30?70° S), resulting in total concentrations of ~250?1000 cm?3, in good agreement with observations. Particle formation tends to peak towards the top of the marine boundary layer and there is a lack of obvious burst-like behaviour at the sea surface. This result suggests that new particle formation in the marine boundary layer could be confused with entrainment from the free troposphere. These first global particle formation simulations reveal some interesting sensitivities. We show, for example, that significant reductions in primary particle emissions may lead to an increase in total particle concentration because of the coupling between particle surface area and the rate of new particle formation. This result suggests that changes in emissions may have a complicated effect on global and regional aerosol properties. Overall, our results show that new particle formation is a significant component of the aerosol particle number budget.

A model for the thermal conductivity of nanofluids – the effect of interfacial layer

Abstract: A model for predicting the effective thermal conductivity of nanofluids is proposed. It has been documented that the interfacial layer at the solid (particle)/liquid interface and particle size is one of the major mechanisms for enhancing the thermal conductivity of nanofluids. Comparing with other classical models, the proposed model takes into account some additional effects including volume fraction, thickness, thermal conductivity of the interfacial layer and particle size. The proposed model is found to be better than the existing models since the predicted effective thermal conductivity of different types of nanofluids are closer to the experimental results.

Stabilization of foams with inorganic colloidal particles

Abstract: Wet foams are used in many important technologies either as end or intermediate products. However, the thermodynamic instability of wet foams leads to undesired bubble coarsening over time. Foam stability can be drastically improved by using particles instead of surfactants as foam stabilizers, since particles tend to adsorb irreversibly at the air-water interface. Recently, we presented a novel method for the preparation of high-volume particle-stabilized foams which show neither bubble growth nor drainage over more than 4 days. The method is based on the in-situ hydrophobization of initially hydrophilic particles to enable their adsorption on the surface of air bubbles. In-situ hydrophobization is accomplished through the adsorption of short-chain amphiphiles on the particle surface. In this work, we illustrate how this novel method can be applied to particles with various surface chemistries. For that purpose, the functional group of the amphiphilic molecule was tailored according to the surface chemistry of the particles to be used as foam stabilizers. Short-chain carboxylic acids, alkyl gallates, and alkylamines were shown to be appropriate amphiphiles to in-situ hydrophobize the surface of different inorganic particles. Ultrastable wet foams of various chemical compositions were prepared using these amphiphiles. The simplicity and versatility of this approach is expected to aid the formulation of stable wet foams for a variety of applications in materials manufacturing, food, cosmetics, and oil recovery, among others.

Effect of Pd nanoparticle size on the catalytic hydrogenation of allyl alcohol.

Abstract: We report a particle size dependence for the rate of hydrogenation of allyl alcohol using 1.3−1.9 nm Pd dendrimer-encapsulated nanoparticle (DEN) catalysts. For particles with diameters of <1.5 nm and containing <147 Pd atoms, the modulation in catalytic activity is due to the electronic properties of the particle. For the larger particles, 1.5−1.9 nm in diameter and containing an average of 147−250 Pd atoms, the size effect is a result of geometrical constraints. Specifically, the hydrogenation reaction is shown to occur preferentially on the face atoms of the larger nanoparticles.

Understanding the mechanism of aluminium nanoparticle oxidation

Abstract: Aluminium nanoparticles have gained importance in the last decade because of their increased reactivity as compared with traditional micron-sized particle. The physics of burning of aluminium nanoparticle is expected to be different than that of micron-sized particles, and the current article is motivated by these differences. We have previously measured the size resolved reactivity of nanoaluminium by single-particle mass spectrometry, to which we now add transmission electron microscope (TEM) and an on-line density measurement. The latter two studies revealed the presence of hollow particles following oxidation of nanoaluminium and indicating the significance of diffusion of aluminium in the overall process. Based on experimental evidence, we believe that aluminium nanoparticle oxidation occurs in two regimes. Prior to melting of aluminium slow oxidation occurs through the diffusion of oxygen through the aluminium oxide shell. Above the melting point, we transition to a fast oxidation regime whereby bot...