We present an old and regretfully forgotten method by Jacobi which allows one to find many Lagrangians of simple classical models and also of nonconservative systems. We underline that the knowledge of Lie symmetries generates Jacobi last multipliers and each of the latter yields a Lagrangian. Then it is shown that Noether's theorem can identify among those Lagrangians the physical Lagrangian(s) that will successfully lead to quantization. The preservation of the Noether symmetries as Lie symmetries of the corresponding Schrödinger equation is the key that takes classical mechanics into quantum mechanics. Some examples are presented.
We present an old and regretfully forgotten method by Jacobi which allows one to find many Lagrangians of simple classical models and also of nonconservative systems. We underline that the knowledge of Lie symmetries generates Jacobi last multipliers and each of the latter yields a Lagrangian. Then it is shown that Noether's theorem can identify among those Lagrangians the physical Lagrangian(s) that will successfully lead to quantization. The preservation of the Noether symmetries as Lie symmetries of the corresponding Schrödinger equation is the key that takes classical mechanics into quantum mechanics. Some examples are presented.
We study classical and quantum dynamics of the symmetric harmonic oscillator and the symmetric bouncer defined in 2-D. For these systems we get each of them for two different constants of motion, two Lagrangians and two Hamiltonians which describe the same classical dynamics. However, the quantization of these systems (using Schrödinger equation), using their two equivalents Hamiltonian, describes different quantum dynamics for each of them. This represents an ambiguity on the Hamiltonian formulation of the Quantum Mechanics.
One classical theory, as determined by an equation of motion or set of classical trajectories, can correspond to many unitarily {\em in}equivalent quantum theories upon canonical quantization. This arises from a remarkable ambiguity, not previously investigated, in the construction of the classical (and hence the quantized) Hamiltonian or Lagrangian. This ambiguity is illustrated for systems with one degree of freedom: An arbitrary function of the constants of motion can be introduced into this construction. For example, the nonrelativistic and relativistic free particles follow identical classical trajectories, but the Hamiltonians or Lagrangians, and the canonically quantized versions of these descriptions, are inequivalent. Inequivalent descriptions of other systems, such as the harmonic oscillator, are also readily obtained.
The time-dependent Schrödinger equation is a cornerstone of quantum physics and governs all phenomena of the microscopic world. However, despite its importance, its origin is still not widely appreciated and properly understood. The quantization of the forced harmonic oscillator is studied with the quantum variable (
x ,
v^) , with the commutation relation [
x ,
v^] =
iℏ/
m , and using a Schrödinger’s like equation on these variable, and associating a linear operator to a constant of motion
K(
x,v,t) of the classical system, The comparison with the quantization in the space (
x,p) is done with the usual Schrödinger’s equation for the Hamiltonian
H(
x,p,t), and with the commutation relation [
x ,
p^] =
iℏ. It is found that for the non-resonant case, both forms of quantization bring about the same result. The difference means that the H-approach case brings about more complex behavior in the quantum dynamics than the K-approach case, and that the H-approach case losses more information than the K-approach case.However, for the resonant case, both forms of quantization are different, and the probability for the system to be in the exited state for the (
x ,
v^) quantization has fewer oscillations than the (
x ,
p^) quantization, the average energy of the system is higher in (
x ,
p^) quantization than on the (
x ,
v^) quantization, and the Boltzmann- Shannon entropy on the (
x ,
p^) quantization is higher than on the (
x ,
v^) quantization. The parameter does not appear to be suitable for experimental measurement because the variation in the average value of the energy is quite modest. Entropy is a nice parameter to investigate experimentally because it differs significantly.