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Metallic shells

Design Methods for Calciners In indirect-heated calciners, heat transfer is primarily by radiation from the cyhnder wall to the solids bed. The thermal efficiency ranges from 30 to 65 percent. By utilization of the furnace exhaust gases for preheated combustion air, steam produc tion, or heat for other process steps, the thermal efficiency can be increased considerably. The limiting factors in heat transmission he in the conductivity and radiation constants of the shell metal and solids bed. If the characteristics of these are known, equipment may be accurately sized by employing the Stefan-Boltzmann radiation equation. Apparent heat-transfer coefficients will range from 17 J/(m s K) in low-temperature operations to 8.5 J/(m s K) in high-temperature processes. [Pg.1211]

The first ionization energy is highest for elements close to helium and is lowest for elements close to cesium. Second ionization energies are higher than first ionization energies (of the same element) and very much higher if the electron is to be removed from a closed shell. Metals are found toward the lower left of the periodic table because these elements have low ionization energies and can readily lose their electrons. [Pg.168]

For example, clusters identified by IR spectra and extraction as Ir4(CO)i2 on y-Al203 were found by EXAFS spectroscopy to have an Ir-Ir coordination number of nearly 3, consistent with the tetrahedral structure of the metal frame EXAFS spectroscopy produces the equivalent result for sohd Ir4(CO)i2 [27]. EXAFS spectroscopy is the most appropriate method for determination of framework structures of supported clusters, but it is limited by the errors to clusters with at most about six metal atoms. Thus, it has been used to determine frameworks that are triangular (EXAFS first-shell metal-metal coordination number of 2), tetrahedral (EXAFS first-shell metal-metal coordination number of 3), and octahedral (EXAFS first-shell metal-metal... [Pg.218]

In order to realize the precise control of core/shell structures of small bimetallic nanoparticles, some problems have to be overcome. For example, one problem is that the oxidation of the preformed metal core often takes place by the metal ions for making the shell when the metal ions have a high-redox potential, and large islands of shell metal are produced on the preformed metal core. Therefore, we previously developed a so-called hydrogen-sacrificial protective strategy to prepare the bimetallic nanoparticles in the size range 1.5-5.5nm with controllable core/shell structures [132]. The strategy can be extended to other systems of bi- or multimetallic nanoparticles. [Pg.56]

Figure 5.239. Response of the shell, metal and tube temperature corresponding to Fig. 5.238. Figure 5.239. Response of the shell, metal and tube temperature corresponding to Fig. 5.238.
Although two closed-shell metal cations with the same charge would normally be expected to repel each other, evidence has been obtained for an entire family of cation-cation interactions in dlh or s2 systems.570 This attraction is now shown to originate from dispersion (van der Waals)... [Pg.605]

Already in the early twentieth century it was realized that definitions such as (D1) do not adequately cover all units of interest in chemistry. Thus, by 1902 Werner had demonstrated (Section 4.5.1) that numerous covalently saturated ligand (L) species (L = CO, NH3, H20, etc.) could exist both as free molecular species and in coordinated form as components of transition-metal complexes ML with open-shell metals M,... [Pg.580]

Neglect the tube and shell metal. Tune PI controllers experimentally for each system. Find the outlet temperature deviations for a 25 percent step, increase in process flow rate. [Pg.241]

The metal-ligand interaction in S complexes should he comparable to that in other complexes with sulfur-containing ligands, at least for higher values of n. Additionally, the observation that polysulfides with even n prefer coordination to closed-shell metal ions and those with odd n to open-shell ones indicates that the kind of metal-to-ligand interaction is obviously not restricted to the sulfur atoms attached directly to the metal. [Pg.116]

We shall examine briefly the photoemission (XPS) binding energies (Et, relative to Ep) of core levels for open shell metals. An ample discussion has been developed in this matter, leading to a satisfactory agreement between theoretical models and experimental spectroscopic results. For the purpose of this book, the theoretical model employed is relevant... [Pg.212]

In open shell metals, these empty states can be d- or f-states somewhat hybridized with band states (see Chap. A). In a metal, these states may be pulled down into the conduction band (as a virtual state, see Chap. A) in a compound, presenting a ligand valence band (insulator or semiconductor), they may be pulled down to an energy position coinciding with or very near to this valence band (as a true impurity level). The two possible final states (Eqs. 22 a and 22 b) explain the occurrence of a split response one of the crystal band electrons occupies either the outer hole level P (Eq. 22 a) or the more bandlike hole B " (Eq. 22 b). [Pg.215]

Detailed Examination of Parts. Sometimes it is necessary to take the igniter apart and submit the shell (metal or plastic), the wires, sealing compound and igniter compound to a physical and chemical examination. The disassembly operation should be carried out behind a barricade, preferably by remote control. The tests are usually different for each type of igniter and are described in the corresponding specifications... [Pg.274]

MCD can be particularly useful in the study of enzymes containing open-shell metal ions because of its sensitivity to the electronic structure at the active site. [Pg.94]

Ionic States Resulting from Lower Energy Ionizations of Open-Shell Metal Dialkylamides... [Pg.121]

In Dr. M. Gratzel s plenary lecture at IPS-2000,103 he presented the following research topics to improve DSC. 1) Mastering the interfaces, electron transfer dynamics, control of dark current. 2) Charge transport in nanocrystalline films. 3) Panchromatic sensitizers, dye cocktail, quantum dot charge injection. 4) Light management, mixed metal oxide films, core-shell metal oxide films. 5) New... [Pg.179]

As described above, among the several closed-shell metal ions that form luminescent supramolecular entities with gold, thallium(I) forms the most numerous examples. While aurophilic attractions can be considered the upper extreme of the metallophilic interactions (with values up to 46 kJ mol-1), intermetallic contacts involving T1(I) centers appear as the weakest ones (even <20 kJ mol-1),46 which is explained by the enhancement of the Au---Au interactions and the weakening of the Van der Waals attractions between the s2 metal atoms produced by the relativistic effects.47 Nevertheless, the complexes in which this interaction appears are surprisingly stable, with additional electrostatic, packing forces, or the ligand architecture, responsible for this fact. [Pg.343]


See other pages where Metallic shells is mentioned: [Pg.1204]    [Pg.745]    [Pg.351]    [Pg.219]    [Pg.26]    [Pg.55]    [Pg.55]    [Pg.40]    [Pg.640]    [Pg.654]    [Pg.912]    [Pg.207]    [Pg.342]    [Pg.389]    [Pg.178]    [Pg.42]    [Pg.198]    [Pg.212]    [Pg.235]    [Pg.20]    [Pg.407]    [Pg.4]    [Pg.65]    [Pg.200]    [Pg.45]    [Pg.60]    [Pg.151]    [Pg.571]    [Pg.853]    [Pg.196]    [Pg.78]   
See also in sourсe #XX -- [ Pg.28 ]




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Amorphous silicon-metal core-shell

Bonding in Open-Shell Transition-Metal Complexes

Closed-shell transition metal atom states

Clusters metallic, shell structure

Core-shell metal nanoparticles

Core-shell metal nanoparticles research

Core-shell metal/polymer nanoparticles

Double-shell effect, transition metal

Growth of Silica Shells on Metal Nanoparticles

Metal particles core/shell structured bimetallic

Metal valence shell

Metal-core/polymer-shell hybridized

Metal-core/polymer-shell hybridized nanocrystals

Open-shell transition metal ions

Open-shell transition-metal complexe

Open-shell transition-metal complexe molecules

Polymer-core/metal-shell

Semiempirical method for transition metal complexes with open (-shells

Shell Model metal oxides

The Luminescence of Closed-Shell Transition-Metal Complexes

Transition Metals Have Electron Configurations with Incomplete d or f Shells

Transition metal ions hydration shell

Transition metal valence shell, filled

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