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Ionic cations and anions

Ionic Cations and anions Electrostatic, non-directional Hard, brittle, crystals of high m.t. moderate insulators melts are conducting Alkali metal halides... [Pg.67]

P , P+, P designate non-ionic, cationic, and anionic polymers, respectively. [Pg.601]

With respect to the properties of polar groups, surfactants can be subdivided into ionic (cation- and anion-active, ampholytic, and zwitterionic) and nonionic surfactants. If the effect produced by the polar group of the surfactant molecule is more significant than that of the lipophilic group, this substance is soluble in water. It is less surface active as compared to any substance characterized by an optimum balance between the activities of hydrophilic and lipophilic groups. Similar conclusions can be drawn also with respect to the solubility in oil here, the role of the lipophilic group is determining. Clearly, the efficiency of a surfactant is not determined solely by the amphiphilicity, but depends on the hydrophilic/lipophilic balance (HLB) characteristic for this compound. Therefore, this balance is an important characteristic of both the surfactant and the interface. [Pg.36]

Polystyrene is one of the most important commodity polymers and perhaps the most well-known and most extensively studied polymers. Styrene can be polymerized by free-radical polymerization, ionic (cationic and anionic) polymerization, and coordination polymerization. Free-radical polymerization is most frequently used to produce atactic polystyrene. Ionic polymerization is used to prepare polystyrene of narrow molecular-weight distribution. Because styrene reacts readily with many other vinyl monomers and rubbers, a wide variety of styrene copolymers are commercially available. There are many styrene copolymers commercially available, but the following four styrene polymers are of particular importance ... [Pg.316]

Before the development of CRP methods, ionic (cationic and anionic) or metal-catalysed polymerisations were efficient techniques for the synthesis of glycopolymers with controlled architectures. However, the use of ionic polymerisations quickly became limited because of the harsh polymerisation conditions and the requirement for protected monomers. Anionic polymerisation was limited to vinyl monomers possessing electron-withdrawing groups (nitrile, carbonyl) and required aprotic solvents and low reaction temperatures [ 110-112]. With the development of metal-based catalysis, which was tolerant to a number of functional groups, ring-opening metathesis... [Pg.21]

Ionic Cations and anions Electrostatic attractions Hard moderate to very high melting points nonconductors as solids, but good electric conductors as liquids many are soluble in polar solvents such as water NaCl,MgO, NaNOs... [Pg.547]

Kapustinskii equation For an ionic crystal composed of cations and anions, of respective charge and z, which behave as hard spheres, the lattice energy (U) may be obtained from the expression... [Pg.230]

Madeluag constant For an ionic crystal composed of cations and anions of respective change z + and z, the la ttice energy Vq may be derived as the balance between the coulombic attractive and repulsive forces. This approach yields the Born-Lande equation,... [Pg.245]

One of the major factors in determining the structures of the substances that can be thought of as made up of cations and anions packed together is ionic size. It is obvious from the nature of wave functions that no ion has a precisely defined radius. However, with the insight afforded by electron... [Pg.309]

The equivalent conductivity of an electrolyte is the sum of contributions of the individual ions. At infinite dilution A° = A° -f A, where A° and A are the ionic conductances of cations and anions, respectively, at infinite dilution (Table 8.35). [Pg.996]

DeioniZa.tlon, The removal of cations and anions from water and replacement of them with hydrogen and hydroxide ions is called deionization. The completeness of the ionic removal is dependent on resin selection, design of the system, operating conditions, and the quaUty of treated water required. In general, systems become more complex as quaUty requirements increase. [Pg.386]

Electrodialysis. In reverse osmosis pressure achieves the mass transfer. In electro dialysis (qv), dc is appHed to a series of alternating cationic and anionic membranes. Anions pass through the anion-permeable membranes but are prevented from migrating by the cationic permeable membranes. Only ionic species are separated by this method, whereas reverse osmosis can deal with nonionic species. The advantages and disadvantages of reverse osmosis are shared by electro dialysis. [Pg.294]

In pure and stoichiometric compounds, intrinsic defects are formed for energetic reasons. Intrinsic ionic conduction, or creation of thermal vacancies by Frenkel, ie, vacancy plus interstitial lattice defects, or by Schottky, cation and anion vacancies, mechanisms can be expressed in terms of an equilibrium constant and, therefore, as a free energy for the formation of defects, If the ion is to jump into a normally occupied lattice site, a term for... [Pg.352]

Ionics, Watertown, Mass. cation and anion Ionics... [Pg.87]

The drermodynamic data for CuaS-FeS (Krivsky and Schuhmann, 1957) show that drese sulphides mix to form approximately ideal ionic liquids. These are molten salts in which the heat of mixing is essentially zero, and die entropy of mixing is related to the ionic fractions of die cations and anions. In the present case die ionic fractions yield values for the activities of the two sulphides... [Pg.339]

It seems obvious to me and to most other chemists that the table of cations and anions that form ionic liquids can and will be extended to a nearly limitless number. The applications will be limited only by our imagination. [Pg.6]

The synthesis of ionic liquids can generally be split into two sections the formation of the desired cation, and anion exchange where necessary to form the desired product (demonstrated for ammonium salts in Scheme 2.1-1). [Pg.8]

The price of ionic liquids is determined by many parameters, such as personnel, overheads, and real production costs. One can imagine that production on a small scale would be mostly determined by the personnel cost and little by the material cost. On a large scale, the material cost should become more important and mainly determine the price of an ionic liquid. This means that the price of a large-scale commercial ionic liquid should be dictated by the price of the cation and anion source. [Pg.30]


See other pages where Ionic cations and anions is mentioned: [Pg.201]    [Pg.421]    [Pg.187]    [Pg.183]    [Pg.229]    [Pg.44]    [Pg.275]    [Pg.314]    [Pg.199]    [Pg.201]    [Pg.421]    [Pg.187]    [Pg.183]    [Pg.229]    [Pg.44]    [Pg.275]    [Pg.314]    [Pg.199]    [Pg.263]    [Pg.415]    [Pg.574]    [Pg.2723]    [Pg.172]    [Pg.471]    [Pg.23]    [Pg.52]    [Pg.387]    [Pg.388]    [Pg.350]    [Pg.599]    [Pg.1512]    [Pg.1726]    [Pg.228]    [Pg.54]    [Pg.127]    [Pg.79]    [Pg.80]    [Pg.578]    [Pg.627]    [Pg.2]    [Pg.18]    [Pg.23]   
See also in sourсe #XX -- [ Pg.735 ]




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Cation anion

Cations and anions

Ionic anionic

Ionic cationic

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