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First-order reactions charge

Example 5.5 Ingredients are quickly charged to a jacketed batch reactor at an initial temperature of 25°C. The jacket temperature is 80°C. A pseudo-first-order reaction occurs. Determine the reaction temperature and the fraction unreacted as a function of time. The following data are available ... [Pg.161]

The alkylation of toluene with acetylene in the presence of sulphuric acid is carried out in a batch reactor. 6000 kg of toluene is charged in each batch, together with the required amount of sulphuric acid and the acetylene is fed continuously to the reactor under pressure. Under circumstances of intense agitation, it may be assumed that the liquid is always saturated with acetylene, and that the toluene is consumed in a simple pseudo first-order reaction with a rate constant of 0.0011 s-1. [Pg.254]

A simple first order reaction following reversible charge transfer is one of the few cases for which an analytical solution to the diffusion-kinetic differential equations can be obtained. For reactions (1) and (2) under diffusion-controlled charge-transfer conditions after a potential step, the partial differential equations which must be solved are (18) and (19). After Laplace transforma-... [Pg.145]

First-order reaction. A reaction whose rate depends on reactant concentration raised to the first power. (13.2) Formal charge. The difference between the valence electrons in an isolated atom and the number of electrons assigned to that atom in a Lewis structure. (9.7)... [Pg.1045]

When an irreversible chemical reaction is coupled to a nemstian electron transfer, the i-E curves can be used to provide kinetic information about the reaction in solution. Consider a nemstian charge-transfer reaction with a following first-order reaction ... [Pg.37]

Finite difference method digital simulation (see Chapter 1.2 in this volume) has been performed for many different reaction mechanisms, and normalized absorbance working curves have been presented for not only current and charge but also absorbance of the various species assumed by the mechanism [58, 59). For first-order or pseudo-first-order reactions, a little-used method for graphical analysis of the data is to plot the absorption-time transients according to Eq. (32) [40, 60]. [Pg.500]

The external potential V t(fi) induces the field — F Ke,(f() and the polarization charge Flnsj- ( (), which gives rise to the first order reaction potential position r. The first order reaction potential... [Pg.70]

FIGURE 4,5 Thermal stability of organic peroxides as indicated by time for decomposition of 50% of the original charge (half-life for first-order reaction). (Data from Wallace and Tiernan Company, Lucidol Organic Peroxides, Lucidol Division, Wallace and Tiernan, Buffalo, NY, 1968.)... [Pg.117]

Digester Control For control purposes at constant sulfidity and alkah charge, the deligniftcation rate is treated as a homogeneous reaction, which is first order with respect to the lignin, % remaining in the wood, —dL jdt = kL. The influence of time, t, and temperature, T (Kelvin), has been incorporated into one term, called the JT-factor (33). [Pg.265]


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