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Reaction calorimetry may be classified as a differential technique since the primary data collected are proportional to rate vs. time. From these data, the starting material or product concentration over time may be obtained by simply taking the integral of a polynomial fit to the experimental curve.
As an example, consider the gas-phase reaction NO 2 + CO → NO + CO 2.If this reaction occurred in a single step, its reaction rate (r) would be proportional to the rate of collisions between NO 2 and CO molecules: r = k[NO 2][CO], where k is the reaction rate constant, and square brackets indicate a molar concentration.
Therefore, it is valid to apply the steady state approximation only if the second reaction is much faster than the first (k 2 /k 1 > 10 is a common criterion), because that means that the intermediate forms slowly and reacts readily so its concentration stays low. The graphs show concentrations of A (red), B (green) and C (blue) in two cases ...
Derivation of equations that describe the time course of change for a system with zero-order input and first-order elimination are presented in the articles Exponential decay and Biological half-life, and in scientific literature. [1] [7] = C t is concentration after time t
When studying urease at about the same time as Michaelis and Menten were studying invertase, Donald Van Slyke and G. E. Cullen [29] made essentially the opposite assumption, treating the first step not as an equilibrium but as an irreversible second-order reaction with rate constant +. As their approach is never used today it is sufficient to ...
This graph is called the "Van 't Hoff plot" and is widely used to estimate the enthalpy and entropy of a chemical reaction. From this plot, − Δ r H / R is the slope, and Δ r S / R is the intercept of the linear fit.
In first-order (linear) kinetics, the plasma concentration of a drug at a given time t after single dose administration via IV bolus injection is given by; = / where: C 0 is the initial concentration (at t=0)
If () is the concentration of a substance at time , its time dependence is given by = where k is the reaction rate constant. Such a decay rate arises from a first-order reaction where the rate of elimination is proportional to the amount of the substance: [39]
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