Particles, nanometer-sized

As with any system, there are complications in the details. The CO sticking probability is high and constant until a 0 of about 0.5, but then drops rapidly [306a]. Practical catalysts often consist of nanometer size particles supported on an oxide such as alumina or silica. Different crystal facets behave differently and RAIRS spectroscopy reveals that CO may adsorb with various kinds of bonding and on various kinds of sites (three-fold hollow, bridging, linear) [307]. See Ref 309 for a discussion of some debates on the matter. In the case of Pd crystallites on a-Al203, it is proposed that CO impinging on the support... 

Polymerization occurs in particles whose dimensions are in the nanometer size range, perhaps 10 times smaller than the particles in suspension polymerization. 

The carbon black in semiconductive shields is composed of complex aggregates (clusters) that are grape-like stmctures of very small primary particles in the 10 to 70 nanometer size range (see Carbon, carbon black). The optimum concentration of carbon black is a compromise between conductivity and processibiUty and can vary from about 30 to 60 parts per hundred of polymer (phr) depending on the black. If the black concentration is higher than 60 phr for most blacks, the compound is no longer easily extmded into a thin continuous layer on the cable and its physical properties are sacrificed. Ionic contaminants in carbon black may produce tree channels in the insulation close to the conductor shield. 

A most useful feature of the agglomeration technique is its ability to work with extreme fines. Even particles of less than nanometer size (ca 10 ° m) can be treated, if appropriate, so that ultrafine grinding can be appHed to materials with extreme impurity dissernination to allow recovery of agglomerates of higher purity. A number of appHcations of Hquid-phase agglomeration have reached either the commercial or semicommercial pilot scale of operation. 

High-resolution transmission electron microscopy (HREM) is the technique best suited for the structural characterization of nanometer-sized graphitic particles. In-situ processing of fullerene-related structures may be performed, and it has been shown that carbonaceous materials transform themselves into quasi-spherical onion-like graphitic particles under the effect of intense electron irradiation[l 1],... 

A value of Rqb for an SEI lOnm thick can be estimated from its values for CPE and CSE by assuming that these solid electrolytes consist of nanometer-sized particles. Thus the expected value for / GB at 30 °C for a lOnm SEI is in the range 10-lOOQcm2, i.e., it cannot be neglected. In some cases it may be larger than the ionic (bulk) resistance of the SEI. This calculation leads us to the conclusion that 7 GB and CGB must be included in the equivalent circuits of the SEI, for both metallic lithium and for LixC6 electrodes. The equivalent circuit for a mosaic-type... 

The uncertainty principle is negligible for macroscopic objects. Electronic devices, however, are being manufactured on a smaller and smaller scale, and the properties of nanoparticles, particles with sizes that range from a few to several hundred nanometers, may be different from those of larger particles as a result of quantum mechanical phenomena, (a) Calculate the minimum uncertainty in the speed of an electron confined in a nanoparticle of diameter 200. nm and compare that uncertainty with the uncertainty in speed of an electron confined to a wire of length 1.00 mm. (b) Calculate the minimum uncertainty in the speed of a I.i+ ion confined in a nanoparticle that has a diameter of 200. nm and is composed of a lithium compound through which the lithium ions can move at elevated temperatures (ionic conductor), (c) Which could be measured more accurately in a nanoparticle, the speed of an electron or the speed of a Li+ ion ... 

The foregoing examples show that hollow polymer capsules with varying composition and sizes of ca. 2-20 micrometers can be produced, either by templating charged (latex particles and biocrystals) or uncharged (organic microcrystals), and that different core removal procedures can be employed. Nanometer-size polymer capsules have also been produced by employing smaller particle templates [107]. 

In heterogeneous catalysis, solids catalyze reactions of molecules in gas or solution. As solids - unless they are porous - are commonly impenetrable, catalytic reactions occur at the surface. To use the often expensive materials (e.g. platinum) in an economical way, catalysts are usually nanometer-sized particles, supported on an inert, porous structure (see Fig. 1.4). Heterogeneous catalysts are the workhorses of the chemical and petrochemical industry and we will discuss many applications of heterogeneous catalysis throughout this book. 

These issues are really major ones in research laboratories dealing with specialty chemicals and first level scale-up. Filterability can be a problem with M catalysts supported on classic materials such as carbon, owing to their tendency to pulverisation to give nanometer-sized catalyst particles that turn out to be very difficult to be recovered and successfully reused. 

The synthesis of MNCGs can be obtained by sol-gel, sputtering, chemical vapor-deposition techniques. Ion implantation of metal or semiconductor ions into glass has been explored since the last decade as a useful technique to produce nanocomposite materials in which nanometer sized metal or semiconductor particles are embedded in dielectric matrices [1,2,4,23-29]. Furthermore, ion implantation has been used as the first step of combined methodologies that involve other treatments such as thermal annealing in controlled atmosphere, laser, or ion irradiation [30-32]. 

Among various methods to synthesize nanometer-sized particles [1-3], the liquid-phase reduction method as the novel synthesis method of metallic nanoparticles is one of the easiest procedures, since nanoparticles can be directly obtained from various precursor compounds soluble in a solvent [4], It has been reported that the synthesis of Ni nanoparticles with a diameter from 5 to lOnm and an amorphous-like structure by using this method and the promotion effect of Zn addition to Ni nanoparticles on the catalytic activity for 1-octene hydrogenation [4]. However, unsupported particles were found rather unstable because of its high surface activity to cause tremendous aggregation [5]. In order to solve this problem, their selective deposition onto support particles, such as metal oxides, has been investigated, and also their catalytic activities have been studied. 

As a result, nanometer-sized metallic Au particles were selectively deposited onto monodispersed polycrystalline ellipsoidal hematite particles without addition of any specific reducing agent, as shown in Figure 5. 

Another type of model electrode uses multilayer electrolytic deposits, which attracted the interest of electrochemists long before physical methods for their structural characterization were introduced. These electrodes were usually characterized by their roughness factors rather than particle size, the former being of the order of 10 -10 (for original references, see the review [Petrii and Tsirhna, 2001]). Multilayer electrolytic deposits have very complex stmctures [Plyasova et al., 2006] consisting of nanometer-sized crystallites joined together via grain boundaries, and hence have very pecuhar electrocatalytic properties [Cherstiouk et al., 2008] they will not be considered further in this chapter. 

Note that for metal nanoparticles supported on porous carbon materials, it is even more difficult to establish the mechanism of the ORR. Indeed, for the above-described thin layer or porous RRDE (Section 15.3), H2O2 has very little chance to escape from the CL and be detected at the ring. H2O2 can readsorb either on Pt particles or on the carbon support, and undergo chemical decomposition or further electrochemical reduction, while diffusing out of the CL. This implies great difficulties in establishing the detailed ORR mechanism on nanometer-sized metal nanoparticles. 

Dependence of the electric field distribution in the double layer on particle size [Zhdanov and Kasemo, 2002 Chen and Kucemak, 2004a, b], which, according to Zhdanov and Kasemo, should result in an increase in the rates of electrochemical reactions on nanometer-sized metal particles. 

Separation of colloids by GPC is an important technical advance that may help in the characterization of novel materials. One such separation was the shape separation of gold particles of nanometer size by GPC on a Nucleogel GFC 1000-8 column using sodium dodecyl sulfate and Brij-35 [polyoxyethylene (23) dodecanol] to modulate the adsorption properties of the colloidal gold.42 Rodlike and spherical particles were separated using UV-VIS detection. 

Chemists have been working for a long time with particles having sizes of nanometers. The novelty of recent developments concerns the ability to make nanostructured substances with uniform particle sizes and in regular arrays. In this way it becomes feasible to produce materials that have definite and reproducible properties that depend on the particle size. The development began with the discovery of carbon nanotubes by Ijima in 1991 (Fig. 11.15, p. 116). 

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