Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Small Ions

Figure 9. Perspective drawing of the crystal structure of Mn508. Small, filled balls represent the Mn4f ions small, open circles mark the positions of the Mn2+ ions. The oxygen atoms are shown as large, open circles. Figure 9. Perspective drawing of the crystal structure of Mn508. Small, filled balls represent the Mn4f ions small, open circles mark the positions of the Mn2+ ions. The oxygen atoms are shown as large, open circles.
Figure 6. Structure of the perovskite-type lithium-ion conductor Li 2yLa057TiO3. The lithium ions (small, gray) and the lanthanum ions (large, gray) are randomly distributed over the A sites, of which 14 percent are vacancies, enabling the lithium ions to be mobile. Titanium forms TiOh octahedra, as shown in yellow. The unit cell is indicated. Figure 6. Structure of the perovskite-type lithium-ion conductor Li 2yLa057TiO3. The lithium ions (small, gray) and the lanthanum ions (large, gray) are randomly distributed over the A sites, of which 14 percent are vacancies, enabling the lithium ions to be mobile. Titanium forms TiOh octahedra, as shown in yellow. The unit cell is indicated.
Fig. 4.—Location of titanium ions (small circles) and oxygen ions (large circles) in the plane (110) of rutile. Fig. 4.—Location of titanium ions (small circles) and oxygen ions (large circles) in the plane (110) of rutile.
While both paracellular and passive transcellular pathways are available to a solute, the relative contribution of each to the observed transport will depend on the properties of the solute and the membrane in question. Generally, polar membrane-impermeant molecules diffuse through the paracellular route, which is dominated by tight junctions (Section III.A). Exceptions include molecules that are actively transported across one or both membrane domains of a polarized cell (Fig. 2). The tight junction provides a rate-limiting barrier for many ions, small molecules, and macromolecules depending on the shape, size, and charge of the solute and the selectivity and dimensions of the pathway. [Pg.238]

Metal ions, small organic molecules, peptides and small proteins are the ligands tested thus far. PLIMSTEX should be applicable to other ligands including nucleic acids and other proteins. PLIMSTEX should have utility for measuring affinities of proteins in complexes as well as alone, and if this works, it may be one of the few techniques that can probe interaction of a ligand with one protein that is interacting with others. [Pg.361]

Fig.1 Schematic structures of a DNA, b butynedioic acid and c KDP. Large striped circles represent potassium ions and medium filled circles oxygen ions. Small filled circles are protons and checkerboard filled circles represent phosphorous ions, d Schematic structure of squaric acid... Fig.1 Schematic structures of a DNA, b butynedioic acid and c KDP. Large striped circles represent potassium ions and medium filled circles oxygen ions. Small filled circles are protons and checkerboard filled circles represent phosphorous ions, d Schematic structure of squaric acid...
Ion formation occurs mainly by protonation (positive ion mode) or deprotonation (negative ion small cations (Na K+). In contrast to ESI, mainly singly charged ions are formed in MALDl MS. Because of the pulsed ion... [Pg.377]

The Smith group has also developed the methodology for making high precision calculations for small systems without invoking the Born-Oppenheimer approximation and have made calculations for two-electron atomic ions, small muonic molecules, and potentials of the screened Coulomb form. Their method for determining nonlinear parameters is now referred to as random tempering.169... [Pg.257]

Fig. 1. The positions of different Mn3+ ions (small spheres) in a monoclinic phase primitive cell. Fig. 1. The positions of different Mn3+ ions (small spheres) in a monoclinic phase primitive cell.
It was found impossible to measure the rate of decomposition by the evolution of gases because the release of these gas bubbles is very slow and erratic. The course of the reaction was followed by analyzing samples for the ammonium ion. Small amounts of the decomposing amalgam were forced through a capillary tube into a chilled solution of an iodate. The ammonium reacted with iodate ion to give iodide ion. The solution was then acidified with acetic acid and the iodine distilled out, collected and titrated with sodium thiosulfate. The method was checked with samples... [Pg.114]

The electrochemical inertness (low values of (iQ seems to correlate with an incomplete electronic sub shell in the free atom, high values of heat of solvation of the ions, small interatomic spacing in lattice, and high coordination numbers. [Pg.342]

FIGURE 13.1 Various types of positively charged ion-penetrable porous particles with fixed charges (large circles with plus sign). Electrolyte ions (small circles with plus or minus signs) can penetrate the particle interior. [Pg.299]

Inorganic Ions Small Molecules, Charged and Uncharged Peptides and Proteins Oligonucleotides and Nucleic Acids... [Pg.135]

Non-aqueous solvents should be purified by careful distillation, special care being taken to eliminate all traces of moisture. Not only arc conductances in water appreciably different from those in non-aqueous media, but in certain cases, particularly if the electrolytic solution contains hydrogen, hydroxyl or alkoxyl ions, small quantities of water have a very considerable effect on the conductance. Precautions should thus be taken to prevent access of water, as well as of carbon dioxide and ammonia from the atmosphere. [Pg.45]

Highly water-insoluble compounds can present a difficulty in CE and, therefore, completely non-aqueous electrolyte systems have been developed for both acidic and basic insoluble compounds. Standard CE methods have been developed and validated for determination of either metal ions, small carboxylic acids and inorganic anions. These compounds have limited or no UV ab.sorbance and, therefore, indirect UV detection is employed. [Pg.105]

Fig. 20. Left hand panel 23 A x 23 A STM image of the (2x1) reconstruction on Nao.67W03(100) taken at +0.4 V sample bias and 1 nA tunnel current. Top right hand panel unrelaxed Nao.sO surface plane. The oxygen ions (large spheres) and sodium ions (small spheres) are assigned their conventional Shannon-Prewitt radii. Bottom right panel schematic of the relaxed (2x1) reconstruction with peroxide-like oxygen ion dimers. Adapted from ref. 298. Fig. 20. Left hand panel 23 A x 23 A STM image of the (2x1) reconstruction on Nao.67W03(100) taken at +0.4 V sample bias and 1 nA tunnel current. Top right hand panel unrelaxed Nao.sO surface plane. The oxygen ions (large spheres) and sodium ions (small spheres) are assigned their conventional Shannon-Prewitt radii. Bottom right panel schematic of the relaxed (2x1) reconstruction with peroxide-like oxygen ion dimers. Adapted from ref. 298.
FIGURE 5.12. Analysis of the birefringence of calcite, CaCOa, in terms of the atomic arrangement in crystals, (a) Stereoview of packing in the crystal. Oxygen atoms stippled, calcium ions small filled circles. [Pg.161]

A coordination number of 6 is common for a metal ion. Small, highly charged cations, such as Be + and Al +, have low coordination numbers, although these coordination numbers are usually higher in crystals than in gases or liquids. For example, beryllium chloride, BeCU, in the gas phase, exists as an isolated linear molecule," with coordination number 2 (not truly ionic) in crystals, however, it exists as a polymeric, bridged structure in which the beryllium has the preferable coordination number of 4 (Figure 15.5). Ionic radii vary somewhat with coordination number, and are shorter if the coordination number is smaller. For example, a cation with a tetrahedral coordination of 4 anions has 93-95% the radius... [Pg.636]

Large atom, weakly bound electrons, diffuse orbitals. Small ionisation energy (I) (easy to form - ve ion) small electron affinity (difficult to form — ve ion)... [Pg.90]


See other pages where Small Ions is mentioned: [Pg.1468]    [Pg.284]    [Pg.9]    [Pg.119]    [Pg.298]    [Pg.656]    [Pg.50]    [Pg.332]    [Pg.357]    [Pg.180]    [Pg.351]    [Pg.206]    [Pg.300]    [Pg.303]    [Pg.21]    [Pg.165]    [Pg.114]    [Pg.221]    [Pg.25]    [Pg.288]    [Pg.141]    [Pg.734]    [Pg.139]    [Pg.167]    [Pg.146]    [Pg.200]    [Pg.222]    [Pg.159]    [Pg.745]    [Pg.190]   
See also in sourсe #XX -- [ Pg.17 , Pg.21 , Pg.22 , Pg.24 , Pg.25 , Pg.29 , Pg.30 ]




SEARCH



Acetylene with small hydrocarbon ions

Aqueous Solutions Containing Small Hydrophobic Ions or Molecules

Binding of small molecules and ions

Ionic motion small ions

Ions within small pores

Mobilities of Small Ions and Macroions in Electric Fields

Radon and thoron decay products as small ions

Short-Range Interactions between Polyions and Small Ions

Small Ion Distortions and Rattling

Small Li-Ion Rechargeable Batteries

Small Molecules or Ions of Biological Interest

Small ions and organometallic compounds

Small metal ions

Transport of small solutes and ions across membrane interfaces

© 2024 chempedia.info