On The Theory of Time dilation in Chemical Kinetics
Mirza Wasif Baig

TL;DR
This paper unifies chemical kinetics with special relativity, showing how reaction rates and half-lives are affected by observer motion at relativistic speeds, leading to a relativistic theory of chemical kinetics.
Contribution
It introduces a Lorentz-invariant formulation of chemical reaction rates, integrating relativity into existing kinetic theories and explaining time dilation effects in chemical processes.
Findings
Reaction rates depend on observer velocity, exhibiting relativistic time dilation.
Lorentz transformation applies to rate constants, collision frequency, and transition state theories.
Numerical examples demonstrate the theory's applicability to enzymatic and radioactive decay processes.
Abstract
The rates of chemical reactions are not absolute but their magnitude depends upon the relative speeds of the moving observers. This has been proved by unifying theories of chemical kinetics, which are transition state theory, collision theory, RRKM and Marcus theory, with the special theory of relativity. Boltzmann constant and energy spacing between permitted quantum levels of molecules are quantum mechanically proved to be Lorentz variant. The relativistic statistical thermodynamics has been developed to explain quasiequilibrium existing between reactants and activated complex. The newly formulated Lorentz transformation of the rate constant from Arrhenius Equation, of the collision frequency and of the Eyring and Marcus equations renders the rate law also Lorentz variant. For a moving observer moving at fractions of the speed of light along the reaction coordinate the transition…
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