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Metallic particle

Incorporating reinforcing particles that respond to a magnetic field is important with regard to aligning particles to improve mechanical [Pg.228]

Making a polysiloxane electrically conductive is best carried out using anisometric particles such as films and fibers, because of their low values of the percolation threshold for conducting pathways.Nonetheless, roughly spherical particles of carbon black have also been used for this purpose.2 2 The use of layer-like particles is illustrated by functionalized graphene sheets, while needle shapes are illustrated by unmodified or [Pg.229]

Magnetic properties have also been induced into polysiloxanes by incorporation of particles of a ferrite,2 - 266- 267 iron,2 269 or magnetite.22 - 271 ihese materials can show large field-induced elongations,2  [Pg.229]


Figure Bl.22.1. Reflection-absorption IR spectra (RAIRS) from palladium flat surfaces in the presence of a 1 X 10 Torr 1 1 NO CO mixture at 200 K. Data are shown here for tluee different surfaces, namely, for Pd (100) (bottom) and Pd(l 11) (middle) single crystals and for palladium particles (about 500 A m diameter) deposited on a 100 A diick Si02 film grown on top of a Mo(l 10) single crystal. These experiments illustrate how RAIRS titration experiments can be used for the identification of specific surface sites in supported catalysts. On Pd(lOO) CO and NO each adsorbs on twofold sites, as indicated by their stretching bands at about 1970 and 1670 cm, respectively. On Pd(l 11), on the other hand, the main IR peaks are seen around 1745 for NO (on-top adsorption) and about 1915 for CO (tlueefold coordination). Using those two spectra as references, the data from the supported Pd system can be analysed to obtain estimates of the relative fractions of (100) and (111) planes exposed in the metal particles [26]. Figure Bl.22.1. Reflection-absorption IR spectra (RAIRS) from palladium flat surfaces in the presence of a 1 X 10 Torr 1 1 NO CO mixture at 200 K. Data are shown here for tluee different surfaces, namely, for Pd (100) (bottom) and Pd(l 11) (middle) single crystals and for palladium particles (about 500 A m diameter) deposited on a 100 A diick Si02 film grown on top of a Mo(l 10) single crystal. These experiments illustrate how RAIRS titration experiments can be used for the identification of specific surface sites in supported catalysts. On Pd(lOO) CO and NO each adsorbs on twofold sites, as indicated by their stretching bands at about 1970 and 1670 cm, respectively. On Pd(l 11), on the other hand, the main IR peaks are seen around 1745 for NO (on-top adsorption) and about 1915 for CO (tlueefold coordination). Using those two spectra as references, the data from the supported Pd system can be analysed to obtain estimates of the relative fractions of (100) and (111) planes exposed in the metal particles [26].
In the case of metal particles distributed on a support material (e.g. supported catalysts), XPS yields infomiation on the dispersion. A higher metal/support intensity ratio (at the same metal content) indicates a better dispersion [3]. [Pg.1856]

The saturation coverage during chemisorption on a clean transition-metal surface is controlled by the fonnation of a chemical bond at a specific site [5] and not necessarily by the area of the molecule. In addition, in this case, the heat of chemisorption of the first monolayer is substantially higher than for the second and subsequent layers where adsorption is via weaker van der Waals interactions. Chemisorption is often usefLil for measuring the area of a specific component of a multi-component surface, for example, the area of small metal particles adsorbed onto a high-surface-area support [6], but not for measuring the total area of the sample. Surface areas measured using this method are specific to the molecule that chemisorbs on the surface. Carbon monoxide titration is therefore often used to define the number of sites available on a supported metal catalyst. In order to measure the total surface area, adsorbates must be selected that interact relatively weakly with the substrate so that the area occupied by each adsorbent is dominated by intennolecular interactions and the area occupied by each molecule is approximately defined by van der Waals radii. This... [Pg.1869]

Sonoelectrochemistry has been employed in a number of fields such as in electroplating for the achievement of deposits and films of higher density and superior quality, in the deposition of conducting polymers, in the generation of highly active metal particles and in electroanalysis. Furtlienuore, the sonolysis of water to produce hydroxyl radicals can be exploited to initiate radical reactions in aqueous solutions coupled to electrode reactions. [Pg.1943]

Clusters are intennediates bridging the properties of the atoms and the bulk. They can be viewed as novel molecules, but different from ordinary molecules, in that they can have various compositions and multiple shapes. Bare clusters are usually quite reactive and unstable against aggregation and have to be studied in vacuum or inert matrices. Interest in clusters comes from a wide range of fields. Clusters are used as models to investigate surface and bulk properties [2]. Since most catalysts are dispersed metal particles [3], isolated clusters provide ideal systems to understand catalytic mechanisms. The versatility of their shapes and compositions make clusters novel molecular systems to extend our concept of chemical bonding, stmcture and dynamics. Stable clusters or passivated clusters can be used as building blocks for new materials or new electronic devices [4] and this aspect has now led to a whole new direction of research into nanoparticles and quantum dots (see chapter C2.17). As the size of electronic devices approaches ever smaller dimensions [5], the new chemical and physical properties of clusters will be relevant to the future of the electronics industry. [Pg.2388]

Flafner J FI, Bronikowski M J, Azamian B R, Nikolaev P, Rinzier A G, Colbert A T, Smith K A and Smalley R E 1998 Catalytic growth of single-wall carbon nanotubes from metal particles Chem. Phys. Lett. 296 195... [Pg.2407]

The optical properties of metal nanoparticles have traditionally relied on Mie tlieory, a purely classical electromagnetic scattering tlieory for particles witli known dielectrics [172]. For particles whose size is comparable to or larger tlian tire wavelengtli of the incident radiation, tliis calculation is ratlier cumbersome. However, if tire scatterers are smaller tlian -10% of tire wavelengtli, as in nearly all nanocrystals, tire lowest-order tenn of Mie tlieory is sufficient to describe tire absorjDtion and scattering of radiation. In tliis limit, tire absorjDtion is detennined solely by tire frequency-dependent dielectric function of tire metal particles and the dielectric of tire background matrix in which tliey are... [Pg.2910]

Krelbig U and Genzel L 1985 Optical absorption of small metallic particles Surf. Sol. 156 678... [Pg.2921]

The Beckstead-Derr-Price model (Fig. 1) considers both the gas-phase and condensed-phase reactions. It assumes heat release from the condensed phase, an oxidizer flame, a primary diffusion flame between the fuel and oxidizer decomposition products, and a final diffusion flame between the fuel decomposition products and the products of the oxidizer flame. Examination of the physical phenomena reveals an irregular surface on top of the unheated bulk of the propellant that consists of the binder undergoing pyrolysis, decomposing oxidizer particles, and an agglomeration of metallic particles. The oxidizer and fuel decomposition products mix and react exothermically in the three-dimensional zone above the surface for a distance that depends on the propellant composition, its microstmcture, and the ambient pressure and gas velocity. If aluminum is present, additional heat is subsequently produced at a comparatively large distance from the surface. Only small aluminum particles ignite and bum close enough to the surface to influence the propellant bum rate. The temperature of the surface is ca 500 to 1000°C compared to ca 300°C for double-base propellants. [Pg.36]

Fibrillated Fibers. Instead of extmding cellulose acetate into a continuous fiber, discrete, pulp-like agglomerates of fine, individual fibrils, called fibrets or fibrids, can be produced by rapid precipitation with an attenuating coagulation fluid. The individual fibers have diameters of 0.5 to 5.0 ]lni and lengths of 20 to 200 )Jm (Fig. 10). The surface area of the fibrillated fibers are about 20 m /g, about 60—80 times that of standard textile fibers. These materials are very hydrophilic an 85% moisture content has the appearance of a dry soHd (72). One appHcation is in a paper stmcture where their fine fiber size and branched stmcture allows mechanical entrapment of small particles. The fibers can also be loaded with particles to enhance some desired performance such as enhanced opacity for papers. When filled with metal particles it was suggested they be used as a radar screen in aerial warfare (73). [Pg.297]

Particle Contamination. In assembling large, high voltage equipment such as coaxial lines, contamination by metal particles may occur which may decrease the dielectric strength under various conditions by 5 to 10-fold (44—45). Metal needles are the worst contaminants and electrostatic traps or adhesive areas have been designed to cope with them (46). [Pg.242]

The laser spray process uses a high power carbon dioxide laser focused onto the surface of the part to be metallized. A carrier gas such as belium blows metal particles into the path of the laser and onto the part. The laser melted particles may fuse to the surface, or may be incorporated into an aHoy in a molten surface up to 1-mm thick. The laser can be used for selective aHoying of the surface, for production of amorphous coatings, or for laser hardening. [Pg.136]

Whereas many of these technologies are not really new, they have never had the regulatory and economic justification for their use in metallizing. Each of these general methods has many variants. Some may be directed to waste treatment, some to recycle, and some to reclaim. An example is filtration, used to prevent release to air of zinc particles from flame spraying, microfiltration of cleaners to extend hfe, in combination with chemical precipitation to remove metal particles from wastewater, and many other uses. [Pg.140]

Slip casting of metal powders closely follows ceramic slip casting techniques (see Ceramics). SHp, which is a viscous Hquid containing finely divided metal particles in a stable suspension, is poured into a plaster-of-Paris mold of the shape desired. As the Hquid is absorbed by the mold, the metal particles are carried to the wall and deposited there. This occurs equally in all directions and equally for metal particles of all sizes which gives a uniformly thick layer of powder deposited at the mold wall. [Pg.185]

On a given metallic particle, the repulsive force, E, is dependent on particle mass, AF electrical conductivity. O density, p and shape, s. [Pg.430]

The finer soil fraction contains adsorbed organics, small metallic particles, and bound ionic metals. This fraction may be treated further to remove the contaminants, or it may be incinerated or landfilled. The "clean" coarse fraction may contain some residual metallic fragments. With metal contamination, both the fine and coarse soil fractions may be leached with an acid solution to remove the metals. [Pg.173]

Some friction materials may contain other potentially harmfiil materials. Lead has been found in some secondary linings. Class B and C organic disk pads, and other friction materials as lead metallic particles, oxides, and sulfides. Several original equipment and aftermarket suppHers are known to have a pohcy against incorporation of lead or other potentially harmfiil materials in thek products. [Pg.275]

There are only a few weU-documented examples of catalysis by metal clusters, and not many are to be expected as most metal clusters are fragile and fragment to give metal complexes or aggregate to give metal under reaction conditions (39). However, the metal carbonyl clusters are conceptually important because they form a bridge between catalysts commonly used in solution, ie, transition-metal complexes with single metal atoms, and catalysts commonly used on surfaces, ie, small metal particles or clusters. [Pg.169]

Nonconventiona.1 Solder Systems. Nonconventional solder systems are developed for use with newer alloys, especially base metal alloys. They are few in number and will probably remain the exception rather than the rule. Some new solder systems consist of metallic particles either pressed to form a rod or suspended in a paste flux. The metallic composition is close to that of the alloy to be joined. If the particles are nonhomogeneous, the solder has particles with melting points lower and higher than that of the alloy. For nonhomogeneous solders, once the flame has been placed on the parts to be joined and the soldering material, it should not be removed until the flow process is completed. [Pg.488]

However, conductive elastomers have only ca <10 of the conductivity of soHd metals. Also, the contact resistance of elastomers changes with time when they are compressed. Therefore, elastomers are not used where significant currents must be carried or when low or stable resistance is required. Typical apphcations, which require a high density of contacts and easy disassembly for servicing, include connection between Hquid crystal display panels (see Liquid crystals) and between printed circuit boards in watches. Another type of elastomeric contact has a nonconducting silicone mbber core around which is wrapped metalized contacts that are separated from each other by insulating areas (25). A newer material has closely spaced strings of small spherical metal particles in contact, or fine soHd wires, which are oriented in the elastomer so that electrical conduction occurs only in the Z direction (26). [Pg.31]

This article addresses the synthesis, properties, and appHcations of redox dopable electronically conducting polymers and presents an overview of the field, drawing on specific examples to illustrate general concepts. There have been a number of excellent review articles (1—13). Metal particle-filled polymers, where electrical conductivity is the result of percolation of conducting filler particles in an insulating matrix (14) and ionically conducting polymers, where charge-transport is the result of the motion of ions and is thus a problem of mass transport (15), are not discussed. [Pg.35]

The life of a cage may be a few months and may produce 9000 Mg (10,000 tons) of quany rock. A gray-iron cage is used for alumina grinding, with metal particles removed magnetically. The advantage of... [Pg.1847]

These motors are suitable for locations prone to dust, coal dust and metal particles etc. and occasional water spray and I ain (Figures 1.19(a) and (b)). [Pg.21]

This condition applies when the equilibrium content of the slag of the impurity being transfeiTed would be high, but the bulk of the slag is large compared to the volume of the descending metal particle. When is not much less than... [Pg.325]

This reaction is carried out in tall fluidized beds of high L/dt ratio. Pressures up to 200 kPa are used at temperatures around 300°C. The copper catalyst is deposited onto the surface of the silicon metal particles. The product is a vapor-phase material and the particulate silicon is gradually consumed. As the particle diameter decreases the minimum fluidization velocity decreases also. While the linear velocity decreases, the mass velocity of the fluid increases with conversion. Therefore, the leftover small particles with the copper catalyst and some debris leave the reactor at the top exit. [Pg.183]


See other pages where Metallic particle is mentioned: [Pg.257]    [Pg.723]    [Pg.926]    [Pg.953]    [Pg.102]    [Pg.257]    [Pg.581]    [Pg.379]    [Pg.277]    [Pg.547]    [Pg.138]    [Pg.178]    [Pg.91]    [Pg.154]    [Pg.174]    [Pg.162]    [Pg.396]    [Pg.423]    [Pg.426]    [Pg.166]    [Pg.211]    [Pg.238]    [Pg.129]    [Pg.135]    [Pg.204]    [Pg.310]   
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Adsorption of atomic, molecular, and cluster particles on metal oxides

Aggregation of metallic particles

Aggregation parent metal particles

Alloys metal particle size effects

Association with metal particles

Calculation of Metal Surface Area, Dispersion, and Particle Diameter

Cathode nickel metal particle

Characterisation of small Metal Particles

Chemistry of Nanosized Metallic Particles

Colloidal metal particle dispersions

Colloidal metal particle dispersions fabricating

Colloidal metal particles

Combustion of Metal Particles

Composite particles metal oxides

Conductive composites metal particle

Copper with metallic particles

Correlation between Metal Particle Size and Reaction Mechanisms

Cubic metal particles

Cyclopentane, hydrogenolysis, metal particle

Dechlorination metal particles

Defective or Doped Graphene as a Support for Transition Metal Particles

Effect of Metal Particles on Combustion Stability

Electron microscopy, small metal particle

Electronic Properties of Small Metal Particles

Ethane metal particle size effect

Experimental and theoretical developments in small metal-particle catalysis using electron microscopy

Fillers metal particles

Fine metal particle

Graphite surfaces, interaction metal particles

Group VIII metal particles

Group VIII metal particles complexes

Harutas Mechanism Metal Gold Particles

Heavy metal particles

Heterogeneous catalysts supported metal particle preparation

Hollow Particles of Other Metal Oxides

Hollow metal oxide particles

Hydrocarbons metal particle size effects

INDEX metal particle size distribution

Image contrast and visibility of supported small metal catalyst particles in HRTEM

Imaging Supported Metal Particles in the TEM

Iron metal particles

Line-broadening analysis, metal particle size

Measurement of Potentials at Semiconductor and Metal Particles Under Irradiation

Metal Particles as Fuel Components

Metal Particles on Oxides

Metal carbides particle size

Metal catalysts particle size

Metal clusters decomposition, small particle

Metal coated latex particles

Metal colloid particles, electrostatic stabilization

Metal colloid synthesis particles, mechanism

Metal hydrous oxide particles

Metal oxide particles

Metal oxide-based compounds particle size

Metal particle composites

Metal particle composites distributions

Metal particle composition and size

Metal particle composition and size dependence

Metal particle dispersion

Metal particle nanocomposites

Metal particle nanosize

Metal particle preparation

Metal particle size

Metal particle size contributions

Metal particle size dependence

Metal particle, physical model

Metal particle-polymer composite

Metal particle-polymer composite materials

Metal particles

Metal particles -polymer

Metal particles bonds

Metal particles catalysts

Metal particles composition

Metal particles core/shell structured bimetallic

Metal particles electrochemical synthesis

Metal particles from neutral complexes

Metal particles in zeolites

Metal particles resonance line

Metal particles shape

Metal particles solutions

Metal particles stabilization

Metal particles structure

Metal particles surfaces

Metal particles, as catalysts

Metal particles, chemical principles

Metal particles, surface plasmon effects

Metal pollution particle-water interactions

Metal-dust particles

Metal-perovskite catalysts particles

Metal-to-particle charge-transfer

Metallic and Catalytic Particles

Metallic and ceramic particles

Metallic latex particles

Metallic particles as catalysts

Metallic particles, encapsulation

Metallic silver particles

Metals particle formation

Microcrystalline metal particles

Microscopic metals bimetallic particles

Morphology of Metal Particles

Nano-sized metal particles

Nano-sized metal particles assemblies

Nano-sized metal particles chemical properties

Nano-sized metal particles physical properties

Nano-sized metal particles properties

Nano-sized metal particles synthesis

Nanodispersed metal particles in polymeric

Nanometer-sized metal particles

Nanometer-sized metal particles, surface

Nanoscale metal particles

Nanosized metal particles

Nanostructured metal particles, optical

Noble metal particles, influence

Noble metal particles, influence materials

Noble metal particles, redox-active

On the Size-Induced Metal-Insulator Transition in Clusters and Small Particles

Ophthalmic ointments metal particles

Particle nucleation and sintering in supported metal catalysts

Particle reinforced metals

Particle size distribution, of metal

Particle size effect metal loading

Particle size effects supported metal catalysts

Particle size metal oxide-mica pigments

Particle size of metal

Particle-Size Effects with Supported Metals

Particles attached metallic

Particles inert metallic

Particles metal hydride

Particles quasi-metallic

Particles, Residues, and Trace Metals

Particles, Slurry Residues, and Trace Metal

Passivated metal particles

Passivated metal particles Passive” polymer

Polymer, chemical physics colloidal metal particles

Polymer-fine metal particles

Polymer-metal particle interactions

Polymeric electrodeposits with metallic particles

Preparation metal particle formation

Preparation of Supported Metal Particles

Preparation of Unsupported Metal Particles

Preparation of colloidal metal particles

Properties of Small Metal Particles

Quantum-sized metallic particles

Reactivity oxide-supported metal particles

Schwab effect, metal particles

Segregated metallic particles

Segregated metallic particles polymers

Single metal particles

Size and Shape of Small Metal Particles

Small metal particles

Small metal particles EXAFS

Small metal particles Mossbauer spectroscopy

Small metal particles XANES,

Small metal particles chemisorption

Small metal particles electronic properties

Small metal particles energetic properties

Small metal particles particle size effect

Small metal particles size distribution

Small metal particles structure

Small metal particles theoretical methods

Small metal particles transmission electron microscopy

Small metal particles turnover frequency

Small metal particles, properties

Spatial Distribution of Electrodeposited Metal Particles

Spectroscopy as a Probe of Surface Electrochemistry at Metal Catalyst Particles

Structure of small metal particles

Supported catalysts, electronic state metallic particles

Supported metal-particle catalysis

Supported metals, small particles

Supported metals, small particles alloying effects

Supported metals, small particles bonding with support

Supported metals, small particles characteristics, 157

Supported metals, small particles compounds

Supported metals, small particles coprecipitation

Supported metals, small particles crystal structure change

Supported metals, small particles dispersion

Supported metals, small particles distribution

Supported metals, small particles electron microscopy

Supported metals, small particles electronic properties

Supported metals, small particles impregnation

Supported metals, small particles particle size

Supported metals, small particles preparation methods, 61

Supported metals, small particles reconstruction

Supported metals, small particles specific catalysts

Supported metals, small particles structure sensitivity

Syngas metal particles

Synthesis with Supported Metal Particles by Use of Surface Organometallic Chemistry Characterization and some Applications in Catalysis

The Structures and Compositions of Colloidal Metal Particles

The sintering of solid metal particles

Titania interaction with metal particles

Water-atomized metal particles

Zeolite with finely dispersed metal particles

Zeolites metal particle formation

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