𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A method for determining constants of first-order reactions from experimental data

✍ Scribed by W. P. Isaacs; A. F. Gaudy Jr.


Publisher
John Wiley and Sons
Year
1968
Tongue
English
Weight
474 KB
Volume
10
Category
Article
ISSN
0006-3592

No coin nor oath required. For personal study only.

✦ Synopsis


The authors have utilized a previously proposed mathematical equation (introduced originally for development of empirical equations) as a useful tool for evaluation of first-order reaction rate constants. By assigning physical significance to the parameter a, the equation can be utilized in obtaining excellent estimates for limiting boundary values and velocity constants.

A number of processes of interest in the bioengineering field proceed in accordance with first-order kinetics. Two of the most important "reactions1' are physical reaeration in receiving streams and exertion of biochemical oxygen demand. While the order of reaction of the latter process may be subject to much debate, it is usually assumed to proceed with kinetics typical of monomolecular reactions. The kinetic constants are usually determined from experimental data, and many methods have been proposed for the evaluation of the velocity constant, K 1 , and the ultimate BOD, Lo.' However, many of these methods are either so tedious that their use is avoided, or so simplified that they provide only a gross approximation of the constants. It is the purpose of this paper to describe the use of a method for obtaining first-order constants which was originally introduced by Davis2 for use in adjusting data which did not show linearity when plotted on semilogarithmic paper. The authors have found that, in addition to its originally intended use, the method of Davis can be successfully employed to obtain accurate values of first-order reaction constants.

The mathematics of first-order reactions are well known, and only a brief review seems warranted. If the rate of a reaction or a process


πŸ“œ SIMILAR VOLUMES


Multivariate resolution of rank-deficien
✍ J. Saurina; S. HernΓ‘ndez-Cassou; R. Tauler; A. Izquierdo-Ridorsa πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 276 KB πŸ‘ 1 views

The effect of a rank deficiency upon curve resolution in simple kinetic reaction-based systems is studied. Firstly, simulated rank-deficient spectrophotometric data of a mixture of two reagents, each one yielding its own reaction product by a first-order kinetic reaction, are analysed. Four differen

New methods for the determination of the
✍ Stephane Marais; Michel MΓ©tayer; Quang Trong Nguyen; Michel LabbΓ©; Dominique Lan πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 121 KB πŸ‘ 2 views

## Model development for transient permeation In the experimental differential permeation technique, the upstream face of a dry polymer sheet is put into contact

Gaseous [H3Cβˆ’Clβˆ’Cl]+ Ions from the React
✍ Fulvio Cacace; Giulia de Petris; Federico Pepi; Marzio Rosi; Anna Troiani πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 132 KB πŸ‘ 2 views

The structure, stability, and reactivity of the [C,H 3 ,Cl 2 ] ions from the reaction of Cl 3 with CH 4 were studied by structurally diagnostic mass spectrometric techniques and by computational methods. The ionic products were characterized as protonated dichloromethane [ClH 2 CΓ€ClH] (1), the more