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Equation charged mixture

A stoichiometric mixture of 3.677 g. (20 mg. atoms) of tungsten powder, 2.318 g. (10 mmoles) of tungsten(VI) oxide, and 4.795 g. (30 mmoles) of bromine is placed in the reaction tube, and a small excess of 3-5 mg. of bromine per milliliter of tube volume is added. After the preliminary heating, the tube is placed in a temperature gradient of 580/450°C. with the charge mixture at the hotter end of the furnace. After about 100 hours the charge is completely transported to the cooler end of the furnace, and the reaction tube is reversed in order to purify the crude product. The equation for the transport reaction is ... [Pg.120]

Section 5.5 dwelled on the transport of charged mixtures and the derivation of the basic transport equations. Recall that for an infinite diluted mixture, the transport of ions takes place due to their migration in the electric field, diffusion and convection. As in the Section 5.5, we limit ourselves to the study of a binary electrolyte mixture, for which (in the case of electrically neutral mixture) the distribution of reduced ion concentration is described by a convective diffusion equation, with the effective diffusion coefficient given by (5.96). The solution of Eq. (5.94) allows us to find the distribution of electric potential. In Eq. (5.98), we can form scalar products of both parts with dx, where x is the radius-vector, and then use the relation between diffusion coefficients of ions and their mobility D = ATi> . Integrating the resultant expression, we then find the potential difference Ap between two points of the mixture ... [Pg.167]

To illustrate the use of these equations, consider a charge of 520 mol of an ethanol-water mixture containing 18 mole percent ethanol to be distilled at 101.3 kPa (1 atm). Vaporization rate is 75 moFh, and the product specification is 80 mole percent ethanol. Let L/V = 0.75, corresponding to a reflux ratio R = 3.0. If the system has seven theo-... [Pg.1336]

For a batch differential distillation where no reflux is used, there is only boilup of a mixture of the desired lighter component, which leaves the kettle, and a desired residual bottoms composition is left in the kettle. This type of distillation follows the Raleigh equation to express the material balance. However, while simple, not having tower packing or trays or reflux does not offer many industrial applications due to the low purities and low yields involved. Repeated charges of the distillate back to the kettle and redistilling w411 improve overhead purity. [Pg.47]

Homobenzvalene (HB) is an electron-rich donor (IP = 8.02 eV) owing to the presence of a strained ring system, and thus readily forms a charge-transfer complex with TCNE. Charge-transfer irradiation of the [HB, TCNE] complex leads to rapid bleaching of the yellow color, and the formation of a mixture of isomeric cycloadducts208 (equation 73). [Pg.266]

As described above, the charge-transfer irradiation of the [HB, TCNE] complex produces the contact ion pair, in which the strained HB+ undergoes multiple bond cleavages to afford three isomeric cation radicals depicted in Scheme 19, which then undergo coupling with TCNE- to form a mixture of isomeric cycloadducts (A, B, and C) in equation (73).208... [Pg.266]

The thermal reaction of the [HB, TCNE] complex leads to a different mixture of isomeric adducts compared to those obtained by charge-transfer cycloaddition208 (equation 74). [Pg.266]

The thermal electron-transfer (ET) via the charge-transfer (CT) equilibrium depicted in equation (86) is established by temperature dependent (UV-vis) spectral studies. For example, an equimolar mixture of hydroquinone ether MA and NO + salt at low temperatures (—78°C) immediately forms the purple [MA, NO+] charge-transfer complex (lmax = 360 nm). However, upon warming the solution an orange-red color of the MA+ cation radical (Amax = 518 nm) develops, and the intensity increases with increasing temperature. Moreover, the identity of liberated NO is confirmed by the quantitative analysis of the head gas with a diagnostic N—O stretching band at 1876 cm -1 in the infrared... [Pg.288]

In this equation, Eis Faraday s constant, the product of Avogadro s constant and the charge on an electron. Since fuel, not a mixture of O2, is fed to the anode, PCOj is assumed to be fixed by the equilibrium relationship. For example, with H2 as the fuel... [Pg.609]

Raman spectroscopy has up to now mainly been applied to elucidate conformational forms and associated conformational equilibria of the IL components. Yet other applications are appearing in these years. One example is the characterization of metal ions like Mn, Ni Y Cu Y and Zn + in coordinating solvent mixtures by means of titration Raman Spectroscopy [118]. Another issue is the study of solvation of probe molecules in ILs. In such a study [118], for example, acceptor numbers (AN) of ILs in diphenylcyclopro-penone (DPCP) were estimated by an empirical equation associated with a C=C / C=0 stretching mode Raman band of DPCP. According to the dependence of AN on cation and anion species, the Lewis acidity of ILs was considered to come mainly from the cation charge [119]. [Pg.346]


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