We consider the possibility that both classical statistical mechanical systems as well as quantum mechanical time independent systems evolve according to the Hamiltonian H. This suggests that given the energy of the system, the Hamiltonian operating on a density or wavefunction will bring back the density or wavefunction with a weight factor of E, energy. For the quantum mechanical case, E represents a frequency. We argue that it is a frequency for both the quantum and statistical mechanical case, related to how quickly the system interacts under the Hamiltonian. We also examine an aspect of interference in the quantum wavefunction which may be related to a 2x2 model of a particle which cycles back and forth as it moves with an average velocity v in a certain direction. We argue that the plane waves stirred up in a potential (or in the Fourier series of the wavefunction) are associated with periodic time motion (due to zitterbewegung). We argue that as these plane waves interfere, they create a new constant average energy throughout a system with a potential which acts as the period of periodic time behaviour, namely exp(iEt)
We consider the possibility that both classical statistical mechanical systems as well as quantum mechanical time independent systems evolve according to the Hamiltonian H. This suggests that given the energy of the system, the Hamiltonian operating on a density or wavefunction will bring back the density or wavefunction with a weight factor of E, energy. For the quantum mechanical case, E represents a frequency. We argue that it is a frequency for both the quantum and statistical mechanical case, related to how quickly the system interacts under the Hamiltonian. We also examine an aspect of interference in the quantum wavefunction which may be related to a 2x2 model of a particle which cycles back and forth as it moves with an average velocity v in a certain direction. We argue that the plane waves stirred up in a potential (or in the Fourier series of the wavefunction) are associated with periodic time motion (due to zitterbewegung). We argue that as these plane waves interfere, they create a new constant average energy throughout a system with a potential which acts as the period of periodic time behaviour, namely exp(iEt)
The classical Lagrangian L leads to Newton’s second law which is equivalent to an energy-momentum conservation equation. The classical action: A = Integral dt1 L(t1) for a constant velocity v=X/T may be varied with respect X and T i.e dA/dT = -E and dA/dX= p. Thus, one may create a differential equation in (dA/dT)(dA/dt) and dA/dx dA/dx for the EE=pp+momo equation. Alternatively, one may create other differential equations. Quantum mechanical differential equations, however, are quite different with exp(i Action) being a solution. Even this may be written as the solution of a non-Schrodinger equation i.e. id/dt exp(iAction) = -1/2m (d/dx exp(iAction)) (d/dx exp(iAction)) for a free particle. For a constant velocity, exp(iAction) is equivalent to exp(ipx-iEt). We argue that this solution is statistical because it separates x and t (as independent variables) and holds for all x and t. Thus, quantum mechanics seems to be a statistical approach using free solutions exp(ipx-iEt) to create an ensemble as in classical statistical mechanics. A difference, however, is that exp(ipx-iEt) “interferes” even if one only takes the real part cos(px-Et). We consider the case of a particle in a box with infinite potential walls to argue that the periodicity is warranted i.e. positive and negative values (interference). Even though the modulus is 1, exp(ipx-iEt) may be operated on by various generators e.g. d/dx the generator of translations. This is analogous to operations on vectors in linear algebra. As noted above, quantum equations are not only energy-momentum conservation equations. They yield a wavefunction W(x) which is an unusual momentum distribution W(x)=Sum over p a(p) exp(ipx). exp(-iEt) holds overall because average E is the same at each x. Thus, one needs a W(x) which leads to a momentum-energy conservation equation, but also satisfies certain boundary conditions which become linked to spatial density= W*W. This leads to discrete energy levels and also cases of humps and troughs in W(x). We attempt to investigate some of these ideas in this note.
Recently, there has been much activity related to statistical models which aim at describing quantum mechanics. It appears, however, that these models do not discuss the time periodic exp(iEt) nature of wavefunctions, at least in an explicit manner. The purpose of this note is to attempt to examine this periodic nature even though it explicitly disappears when calculating the time independent density. To do this , high and low potential V(x) limits are considered. Given that energies of an oscillator are multiples of a physical frequency (plus a background term) and that sound waves can be absorbed and emitted by artificial atoms (quibits), it seems that the physical nature of exp(iEt) may be important.
In the literature, stochastic approaches employed to derive the Schrodinger equation seem to focus on the idea of a classical spatial density which depends on time and space ie. density(x,t). As a result, d/dt (partial) density appears in various equations such as the continuity and Focker Planck equations. At one point in the derivation the quantum wavefunction is introduced “mathematically” as W(x,t)=sqrt(density(x,t)) exp(i S(x,t)) where S is related to a velocity field through u(x,t)=velocity= d/dx S. From quantum mechanics, -Et becomes a term of S the velocity field. The stochastic/hydrodynamical approaches employ the term du/dt partial = d/dt (partial) d/dx S and then “pull out”” d/dx leaving d/dt (partial) S which yields -E average energy from the -Et term. In this note we argue that for a bound quantum state density(x) so d/dt (partial) density = 0, yet the statistical ideas of quantum mechanics should be present in such a case. Furthermore for the free particle wavefunction exp(ipx-iEt), density=1. In fact, the Schrodinger equation should follow for a free particle even the case of density=1. Stochastic processes seem to be based on equations which consider a change in classical spatial density at a point x in time due to flow in or out or stochastic changes. Quantum processes seem to deal with periodic probability changes from one dimension to another exp(ipx) (2 dimensions) which are somehow related to a physical process of momentum flow. Ultimately one links this process to an energy conservation which does not seem to be the same as a classical stochastic/hydrodynamical approach. In this note we argue that a free particle with a constant momentum p has periodic stochastic processes associated with it through its complex probability change in the region of its wavelength, but that these are linked to creating the momentum p. Furthermore momentum is linked to energy so we argue that the Schrodinger equation is a stochastic equation linking energy and momentum and that time and space are separated i.e. there is no situation of following a change in spatial density in time for a free particle with momentum p. For a bound state, one has a distribution of free particles, but again time is removed from the problem in the sense that it only appears in exp(-iEt) in the wavefunction to again establish a relationship between energy and average momentum and potential. There is again no nonzero d/dt (partial) density term which seems to be key in stochastic equations. Only if one takes a linear combination of energy eigenstates Sum over En an(En) exp(-iEnt) Wn(x) does one obtain the form density(x,t), but we argue that quantum features should already appear in exp(ipx) and the bound state scenario with a zero d/dt (partial) density(x,t). We argue, however, that the Schrodinger equation and fundamental stochastic ideas of quantum mechanics should already be present at the level of exp(ipx).
In classical mechanics, the spatial density d(x) of a particle moving under a conservation of energy law .5mv(x)v(x) + V(x) = E is proportional to 1/v(x). This is obtained from d(x)= dt/T, i.e. the probability to be at x equals the time spent at x divided by the cycle time T. Given that dx=vdt to first order, density is proportional to 1/v(x). Now, d(x) is supposed to match the time independent quantum mechanical density W(x)W(x), where W(x) is the wavefunction, for high energy levels. Thus, one would expect the time a p wave (plane wave) spends at a point should be part of time independent quantum mechanics, but it does not seem to be overtly present. Furthermore, there is the question of T for the quantum mechanical problem. It is known that even for a time-independent solution W(x) has a factor exp(iEt). Thus, it seems time is present, even if it disappears in the density W*(x)W(x). It is argued that W*(x)W(x) = P(x) where P is probability, but W(x) is related to conditional probabilities such as P(x/p) or P(p/x). Thus, these conditional probabilities should be related to time. In an earlier note, we tried to show the time-independent Schrodinger equation implies all p plane waves are cycling with the same frequency E. In this note, we try to find a quantum mechanical representation for P(x,p)=dt/T where dt(x,p) is the time spent at x by a plane wave p and also try to evaluate T.
In a series of notes we examined a 2x2 matrix model which is naturally incorporated into Einstein´s 1905 energy momentum equation p2 + m2 = E2 (1). We showed that it was possible to obtain energy, velocity and momentum matrices, calculate expectation, dispersion values and establish exp(-iHt) as the time evolution operator. From this, we calculated zitterbewegung and the time dependence of other matrices. The purpose of this note is to see if this formalism, established for a relativistic model can also be applied to the nonrelativistic case. Several cases are considered. Next, we try to apply the model to the case of a classical spring, which is related to the production of phonons.In this case, we apply the mathematics of the model to the classical spring, not the model itself. It is found that one can obtain a velocity matrix and find an energy matrix with time evolution of exp(-iHt). Furthermore, it appears that time dependent operator calculations predict classical periodic motion with a period of sqrt(k/m), where k is the spring constant and m the mass.
The classical action: Integral (0,T) dt1 L(v(t1), x(t1),t1) may be varied to find a stationary solution which yields Newton’s second law, a standard procedure in classical mechanics. Is it possible to obtain quantum mechanical motion from this same classical action? We argue that one may write the action for a relativistic/nonrelativistic particle moving at constant speed in terms of X and T i.e. v=velocity=constant=X/T. Varying with respect to X and T yields: d/dT Action = -E and d/dX Action = p. Thus, changing X by delta X yields a change in the action of p delta X which holds for all X because of the constant velocity. If one envisions a periodic function such as exp(i Action), this behaves as exp(ipx) in terms of -id/dX. Thus, there is an intrinsic wavelength related to 1/p. This follows directly from small changes of the Action. Alternatively, one may create a differential equation such as the Klein-Gordon or Schrodinger equation from classical conservation of energy-momentum using id/dT exp(iAction) = E exp(i Action) and -id/dX exp(iAction) = p exp(i Action). We note that exp(ipx) which describes the fluctuational behaviour of the classical Action may have positive and negative values showing that fluctuations may be both positive and negative These negative and positive fluctuations are, however, periodic so there is some systematic behaviour occurring, it seems.. We argue that exp(ipx) is statistical as its modulus is 1, indicating that a free particle has equal probability to be at any x point. For a system with a potential V(x), one may create an ensemble describing fluctuations of all possible p values i.e. W(x)=wavefunciton= Sum over p a(p) exp(ipx). The fluctuations are regular positive and negative, but there is different wavelength behaviour for each p i.e. 1/p so there is interference to yield an average fluctuation pattern i.e. the wavefunction.