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Crystalline poly

As a furtlier example for tire meaning of ex situ investigations of emersed electrodes witli surface analytical teclmiques, results obtained for tire double layer on poly crystalline silver in alkaline solutions are presented in figure C2.10.3. This system is of scientific interest, since tliin silver oxide overlayers (tliickness up to about 5 nm) are fonned for sufficiently anodic potentials, which implies tliat tire adsorjDtion of anions, cations and water can be studied on tire clean metal as well as on an oxide covered surface [55, 56]. For tire latter situation, a changed... [Pg.2751]

Figure C2.11.2. A scanning electron micrograph showing individual particles in a poly crystalline alumina powder. Figure C2.11.2. A scanning electron micrograph showing individual particles in a poly crystalline alumina powder.
Silicon is used in many fonns, from high-purity tliin films to bulk material, which may be crystalline, multi- or poly crystalline and amorjDhous (usually hydrogenated). Silicon is the material discussed tire most in tliis article. Substitutional B and P are tire most common (of many) shallow acceptors and donors, respectively. [Pg.2878]

Properties Kaolin-base dRCF High purity RCF RCF with 2irconia RCF with chromia Poly-crystalline alumina... [Pg.56]

H. P. Klug and L. E. Alexander, X-ray Diffraction Proceduresfor Poly crystalline and Mmorphous Materials, 2nd ed., John Wiley Sons, Inc., New York, 1974. [Pg.383]

The simple model given above does not take account of the facts that industrial refractories are poly crystalline, usually non-uniform in composition, and operate in temperature gradients, both horizontal and vertical. Changes in the coiTosion of multicomponent refractories will also occur when there is a change in the nature of tire phase in contact with the conoding liquid for example in Ca0-Mg0-Al203-Cf203 refractories which contain several phases. [Pg.330]

Recently, with the improvement achieved in the preparation and control of surfaces, a number of approaches have been devoted to the estimation of the pzc of pt(lll).140 197 210 211 These are summarized in Table 29 for convenience of the reader. The value recommended for pc-Pt is also reported for comparison. In three cases the pzc has been estimated indirectly and the value is strikingly close to the pzc of poly crystalline Pt. In view of the heterogeneity of Pt surfaces, this closeness is puzzling and suggests that the phenomenon used to estimate the pzc does not conform to the concept of zero charge. [Pg.167]

Poly crystalline silver layer electrodeposited on a polycrystalline platinum electrode. [Pg.441]

The next step is the hydrogen reduction of the trichlorosilane (Reaction 2 above). The end product is a poly crystalline silicon rod up to 200 mm in diameter and several meters in length. The resulting EGS material is extremely pure with less than 2 ppm of carbon and only a few ppb of boron and residual donors. The Czochralski pulling technique is used to prepare large single crystals of silicon, which are subsequently sliced into wafers for use in electronic devices.1 1... [Pg.223]

Poly crystalline boron nitride films, with a structure similar to rhombohedral boron carbide and a ratio of boron to nitrogen of 3 1, were produced by hot-filament CVD. This work indicates the possible existence of other boron-nitride structures. [Pg.275]

Collins, A., and Taylor, R., Optical Characterization of Poly crystalline ZnS Produced via Chemical Vapor Deposition, Proc. 11th. Conf. on CVD, (K. Spear and G. Cullen, eds.), pp. 626-633, Electrochem. Soc., Pennington, NJ 08534 (1990)... [Pg.344]

Many problems must be solved before practical, reliable, and cost-effective diamond semiconductor devices become available. Yet, the prospects are good, particularly if epitaxial single-crystal or highly oriented poly crystalline diamond can be effectively produced by CVD.P5]... [Pg.362]

Figure 8. Comparison between catalytic properties of Pt(poly-crystalline)/Al203 (Engelhard) and Pt(l 00)/Al203 (morphologically controlled Pt nanoparticles) the NO/CH4 reaction conversion (X) and yield (Y), and the reaction products at 500 °C. Figure 8. Comparison between catalytic properties of Pt(poly-crystalline)/Al203 (Engelhard) and Pt(l 00)/Al203 (morphologically controlled Pt nanoparticles) the NO/CH4 reaction conversion (X) and yield (Y), and the reaction products at 500 °C.
In this section, we will investigate the surface structure of the electrode in the potential range before a surface or bulk oxide starts forming, and will restrict ourselves to the adsorption of atomic oxygen only (not OH ) [Jacob and Scheffler, 2007]. Furthermore, in our simulations, we assume a single-crystal Pt(lll) electrode, which will be compared with the experimental CV curve (Fig. 5.9) for poly crystalline Pt. This simplification is motivated by the fact that our interest here is to describe the general behavior of the system only. [Pg.150]

The drop of the voltammetric crurent is associated with Pt surface oxidation, and the drop on the negative-going mn is due to Reaction (12.9) (surface poisoning by CO) and the Tafehan kinetics of Reaction (12.8). Further, the shift between curves in Fig. 12.13a and b indicates that in the potential range between 0.5 and 0.6 V, methanol oxidation occms with zero or low level atop CO smface intermediate. The amplitudes on Fig. 12.13 on both scans nearly equal to each other indicate a high level of preferential (111) crystallographic orientation of the poly crystalline Pt surface used for this work, as inferred from data in [Adzic et al., 1982]. [Pg.392]

The mechanism of anodic oxidation of CO at polycrystalline Au remains uncertain. Several groups have reported that the voltammetry of Au in acidic electrolytes is straightforward, with a well-formed oxidation wave/peak [Stonehart, 1966 Gibbs et al., 1977 Kita et al., 1985 Sun et al., 1999]. There is, however, no voltammetric evidence for the adsorption of CO on the Au surface, and spectroscopic studies indicate only a weak interaction of CO with poly crystalline Au surfaces in acidic solutions [Kunimatsu et al., 1986 Cuesta et al., 2003]. Moreover, there is little evidence for the formation of oxidizing species at the potential where the oxidation process is observed. Certainly, the oxidation of CO occurs at a potential over 500 mV less positive than that where bulk Au oxide is formed, and, indeed, the formation of this oxide strongly... [Pg.571]

Distinct quadrupole shifts do occur as well in magnetically split spectra of single-crystals, poly crystalline powder or frozen solution samples. In all three cases, the line shifts obey the simple first-order expression at high-field condition. [Pg.107]

For a poly crystalline absorber, where the z-axis is randomly distributed, (4.61) reduces to... [Pg.118]

With h 6) - 1/sin 0)5(0 — Oq), one obtains the same result as given by (4.58), which implies that the anisotropy of the/factor cannot be derived from the intensity ratio of the two hyperfine components in the case of a single crystal. It can, however, be evaluated from the absolute/value of each hyperfine component. However, for a poly-crystalline absorber (0(0) = 1), (4.66) leads to an asymmetry in the quadrupole split Mossbauer spectrum. The ratio of l-Jh, as a function of the difference of the mean square amplitudes of the atomic vibration parallel and perpendicular to the y-ray propagation, is given in Fig. 4.19. [Pg.119]

The anisotropic/factor may also manifest itself in the relative line intensities of Zeeman split hyperfine spectra in a poly crystalline absorber. Expanding f(0) in a power series... [Pg.119]

As a function of the surface potential the electron work function for a given material depends on the state of the surface of that material (adsorption, the presence of surface compounds, etc.). For crystalline substances (see Table 3.1), various crystal faces have various electron work function values, which can be measured for single crystals. For poly crystalline substances, the final value of the electron work function depends on the contribution of the individual crystal faces to the entire area of the phase and the corresponding electron work functions the final value of the work function, however, is strongly dependent on the experimental method used for the measurement. [Pg.165]

Platinum electrodes are made usually from poly crystalline metal the crystal planes at the surface include both the (111) and (100) faces in approximately equal proportions. The electrochemical properties of Pt(lll) and Pt(100) faces are not identical. (Generally, the physical properties of individual metal crystal faces, such as work function, catalytic activity, etc., are different.)... [Pg.319]

The working electrodes, 15 mm diameter discs of poly-crystalline platinum fixed in an araldite body were mechanically polished down to 0.05 nm, dipped in diluted HN03, followed by rinsing with an ultrasonic application. [Pg.138]

Further improvement of the Prussian blue-based transducer presents two principal problems. First, Prussian blue layers are not mechanically stable, especially on smooth electrode surfaces because of their poly crystalline nature. Second, despite the low electrode potential used, the most powerful reductants like ascorbic acid still interfere with sensor response if present in excessive concentrations. [Pg.444]

Solvothermal growth of single crystals or poly crystalline aggregates from hydro-thermal or ammonothermal solution. [Pg.240]


See other pages where Crystalline poly is mentioned: [Pg.1380]    [Pg.2414]    [Pg.2624]    [Pg.2625]    [Pg.2762]    [Pg.86]    [Pg.99]    [Pg.166]    [Pg.156]    [Pg.186]    [Pg.640]    [Pg.79]    [Pg.379]    [Pg.445]    [Pg.522]    [Pg.527]    [Pg.207]    [Pg.503]    [Pg.135]    [Pg.324]    [Pg.42]    [Pg.69]    [Pg.184]   
See also in sourсe #XX -- [ Pg.25 , Pg.30 ]

See also in sourсe #XX -- [ Pg.25 , Pg.30 ]




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Alloy poly crystalline

Chiral liquid-crystalline poly

Crystalline features poly concentration

Crystalline polymers Poly

Crystalline polymers poly dienes

Crystalline-Amorphous Poly(ethylene-butene) Copolymers

Crystallinity of poly

Crystallinity poly

Crystallinity poly

Dynamics crystalline poly

Ferroelectric Liquid Crystalline Poly (meta-phenylene)

Glass transition temperatures, poly -liquid-crystalline polymer

Liquid-crystalline polymer-poly blends

Liquid-crystalline polymer-poly(amide

Liquid-crystalline polymer-poly(amide blends

Poly , crystallin

Poly , crystallin

Poly , crystalline phase structur

Poly , liquid-crystalline behavior

Poly , thermotropic liquid crystalline

Poly , thermotropic liquid crystalline properties

Poly -liquid-crystalline

Poly -liquid-crystalline blends

Poly -liquid-crystalline compatibility

Poly -liquid-crystalline copolymer blends

Poly -liquid-crystalline effect

Poly -liquid-crystalline glass transition temperature

Poly -liquid-crystalline meltviscosity

Poly -liquid-crystalline tensile properties

Poly -liquid-crystalline tensile strength

Poly Semi-crystalline Thermoplastics

Poly correlation between crystalline

Poly crystalline Metals

Poly crystalline Solids

Poly crystalline aggregates

Poly crystalline aggregates crystal size

Poly crystalline and amorphous

Poly crystalline bands

Poly crystalline ceramics

Poly crystalline composites with

Poly crystalline diamond

Poly crystalline forms

Poly crystalline materials

Poly crystalline order

Poly crystalline sample

Poly crystalline structure

Poly crystalline, orthorhombic

Poly crystalline-amorphous

Poly crystallinity extent

Poly crystallinity levels

Poly crystallinity loss

Poly crystallinity, crystallization

Poly liquid crystalline polymers

Poly liquid-crystalline property

Polymers, liquid crystalline poly type

Surface poly crystalline

Unit cell of crystalline poly

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