Classical Motion in Force Fields with Short Range Correlations

We study the long time motion of fast particles moving through time-dependent random force fields with correlations that decay rapidly in space, but not necessarily in time. The time dependence of the averaged kinetic energy 〈p ²(t)〉/2 and mean-squared displacement 〈q ²(t)〉 is shown to exhibit a large degree of universality; it depends only on whether the force is, or is not, a gradient vector field. When it is, 〈p ²(t)〉～t ^2/5 independently of the details of the potential and of the space dimension. The stochastically accelerated particle motion is then superballistic in one dimension, with 〈q ²(t)〉～t ^12/5, and ballistic in higher dimensions, with 〈q ²(t)〉～t ². These predictions are supported by numerical results in one and two dimensions. For force fields not obtained from a potential field, the power laws are different: 〈p ²(t)〉～t ^2/3 and 〈q ²(t)〉～t ^8/3 in all dimensions d≥1.     

Intermittency in the atmospheric surface layer: Unresolved or slowly varying?

We present streamwise velocity structure functions 〈δv_L(τ)〉=〈|v(t+τ)−v(t)|^p〉 (with p=1:5) obtained in the near neutral atmospheric surface layer at the Utah SLTEST site at the highest terrestrial Reynolds number Re_τ=O(10⁶). We show that the occurrence of very large scale coherent oscillations in the streamwise velocity throughout the wall region, interpreted as genuine structural features of the canonical turbulent boundary layer, affects the scaling exponents of the p>3 order structure functions. This results in a slight alteration of the intermittent behavior of the velocity field. It was found that for positive (fast) large scale oscillation of the low-pass filtered velocity signal, deviations from the Kolmogorov K41 prediction (absence of multiscaling) are more marked, as compared to negative (slow) excursion. The results are discussed in terms of convergence of statistics from atmospheric boundary layer measurements.     

Pole approximation in the quasi-free t + p scattering and the t(p,d)d reaction via the t + d interaction

The t(p,p)t and t(p,d)d channels have been investigated in an indirect way through the ²H(t,tp)n and ²H(t,dd)n three-body reactions performed at E _t = 35.5?MeV in quasi-free kinematics. The agreement with direct data supports the pole approximation at energies above the Coulomb barrier.     

Hierarchy of mean multiplicities in pn and π+n interactions at 195 GeV/c

The dependence of the average charged multiplicity, 〈n_X〉, of the system X on |t| and M²_X is studied for the reactions p(π⁺)n→p_fast(p⁺_fast) + X and p(π⁺)n→p_slow + X at 195 GeV/c. For a fixed M²_X, 〈n_X〉 changes significantly among these reactions, yielding a systematic hierarchy of mean multiplicities. The results indicate that a proton emits on the average less charged particles than a pion and more than a neutron.     

Synthesis of MoO2 particles during oxidation of bulk molybdenum samples by supercritical water

It was found that bulk samples of molybdenum 〈Mo〉 are oxidized by supercritical water forming nanoparticles of monocline MoO₂. The average size of nanoparticles obtained at uniform heating of 〈Mo〉 with supercritical water was about 27 nm, and the size of agglomerates of nanoparticles was ≤ 1 μm. From time dependence of the amount of formed H₂ n _H2(t), we have determined kinetic parameters of 〈Mo〉 transition to MoO₂ particles. The dependence dn _H2/dt is characterized by the presence of two pronounced maxima. This is explained by the change of mutual diffusion of H₂ and H₂O molecules along with the growth of thickness of the layer of MoO₂ nanoparticles.     

A mode coupling theory of higher order time correlation functions

Kawasaki's mode coupling theory [Ann. Phys. 61 (1970) 1] is used to compute time correlation functions of the form 〈A_k0(t₀) … A_kn(t_n)〉, where A_k(t) represents some slowly varying quantity. The Gaussian and Bare Vertex approximations are made, thus yielding extremely simple expressions for these higher order correlation functions. These do not contain any bare transport coefficients and suggest relatively simple tests by which the theory could be checked. Examples relating to light scattering in nonequilibrium systems and the hydrodynamics of simple fluids are presented.     

Elastic and inelastic φ photoproduction

The differential cross section of the reaction (γp → pφ) has been measured in the t range 0 ? t ? 0.4 GeV² and for photon energies from 3.0 to 6.7 GeV. In particular for the small t region the measurement accuracy was better than 10%. We obtained for the slope parameter B in an exponential parametrization of the differential cross section dσ/dt = Ae^?Bt values of $\text{B ? 6 ± 0.5}\text{GeV}{}^{\mathrm{?2}}$ which are significantly larger than the slopes obtained by most other experiments at higher t values. This indicates a t dependence of B particularly in the small t region.An energy dependence of the optical point (dσ/dt)_t=0, observed in our measurements, has been explained as a kinematic effect due to the VDM relation. A fit of our measurements is in excellent agreement with all other published values of (dσ/dt)_t=0(γp → φp), this implies that σ_tot(φp) must be essentially energy independent in this energy range.Spin density matrix elements of the φ have been evaluated and an analysis of the helicity amplitudes has been carried out. This analysis confirmed s-channel helicity conservation. Moments of spherical harmonics of the $\text{K}\text{K}$ angular decay distribution have been computed for 10 MeV $\text{K}\text{K}$ mass-bins from threshold to 1.3 GeV. The mass dependence of the normalized moments is generally smooth. Contributing amplitudes have essentially only even moments. The moment 〈Y₂⁰〉/〈Y₀⁰〉 changes sign above the φ mass.Differential cross sections for the inelastic φ production γp → φX have been evaluated for the first time both with respect to t?t_min and M_K. The integrated inelastic cross sections are comparable in size with the elastic ones. The slopes of the differential cross sections dσ/dt appear to become flatter with increasing M_X.     

Analyticity properties and a convergent expansion for the inverse correlation length of the high-temperatured-dimensional Ising model

We show that the inverse correlation lengthm(β) (= mass of the fundamental particle of the associated lattice quantum field theory) of the spin-spin correlation function 〈s _x s _y 〉,x, y εZ ^d , of thed-dimensional Ising model admits the representation $$m(\beta ) = - ln\beta + r(\beta )$$ for small inverse temperaturesβ > 0.r(β) is ad-dependent function, analytic atβ = 0.c _n , the nth β = 0 Taylor series coefficient of r(β) can be computed explicitly from the Z^d limit of a finite number of finite lattice A spin-spin correlation functions 〈s₀s_x〉t>Afor a finite number ofx = (x ₁,x₂, ..., x_d), ¦x¦ = ∑ _i ^d 1¦x_i¦< R(n), where R(n) increases withn. Furthermore, there exists aβ' > 0, such that for eachβ ε (0,β')m(β) is analytic. Similar results are also obtained for the dispersion curve ω(p), ω(p)=ω(0)=m, pε(-π, π]^d?1, of the fundamental particle of the associated lattice quantum field theory.     

Computable upper bounds for the adiabatic approximation errors

For a given Hermitian Hamiltonian H(s)(s∈[0,1])with eigenvalues Ek(s)and the corresponding eigenstates|Ek(s)(1 k N),adiabatic evolution described by the dilated Hamiltonian HT(t):=H(t/T)(t∈[0,T])starting from any fixed eigenstate|En(0)is discussed in this paper.Under the gap-condition that|Ek(s)-En(s)|λ0 for all s∈[0,1]and all k n,computable upper bounds for the adiabatic approximation errors between the exact solution|ψT(t)and the adiabatic approximation solution|ψadi T(t)to the Schr¨odinger equation i|˙ψT(t)=HT(t)|ψT(t)with the initial condition|ψT(0)=|En(0)are given in terms of fidelity and distance,respectively.As an application,it is proved that when the total evolving time T goes to infinity,|ψT(t)-|ψadi T(t)converges uniformly to zero,which implies that|ψT(t)≈|ψadi T(t)for all t∈[0,T]provided that T is large enough.     

Canonical realizations of the lie algebras gl(n, R) and sl(n, R) I. Formulae and classification

The generators of the Lie algebra of the general linear group GL(n, R) and of the special linear group SL(n, R) are, recurrently, expressed through polynomials in the quantum canonical variables p_t and q_t. These realizations are skew-Hermitian, the Casimir operations are realized by constant multiples of identity element and, in dependence on the number of the canonical pairs used, they depend on d(d?1 for sl (n,R)), d = 2, …, n, free real parameters.     

Correlation functions of the transverse Ising chain at the critical field for large temporal and spatial separations

We study the behavior of 〈σ₀^x(t)σ_n^x(0)〉 and 〈σ₀^y(t)σ_n^y(0)〉 for the transverse Ising chain at the critical magnetic field at T = 0. Explicit results are obtained for the three distinct regions where t → ∞ and n → ∞with $\text{0 ?}\text{n}\text{t}\text{<1}$, $\text{1 <}\text{n}\text{t}$, or $\text{t = n + n}{}^{\mathrm{<mtext>1</mtext><mtext>3</mtext>}}\text{(}\text{z}\text{2}\text{)}$ where z is fixed of order one. In this latter region the general Painlevé V solution is shown to reduce to a Painlevé II function. We use our results to discuss the general problem of long-time behavior of Toda equations with slowly decaying initial values.     

A theory of the dielectric loss in the aligned nematic mesophase

A theory of dielectric absorption and dispersion in the nematic phase is developed which does not rely on the use of a nematic “director”. The major features of the spectrum are reproduced by using the fact that the autocorrelation functions 〈μ(0) · υ(t)〉 and 〈υ(t) · μ(0)〉 are no longer symmetry disallowed when the overall sample is anisotropic, as in the aligned nematic. Here μ is the dipole vector of the diffusing molecule and υ the centre of mass linear velocity.     

The Inviscid Burgers Equation with Initial Value of Poissonian Type

We study the discontinuities (shocks) of the solution to the Burgers equation in the limit of vanishing viscosity (the inviscid limit) when the initial value is the opposite of the standard Poisson process p. We show that this solution is only defined for t ε (0, 1). Let T ₀ = 0 and T _n , n≧1, be the successive jumps of p. We prove that for all M > 0 the inviscid limit is characterized on the region x ε (-∞, M], t ε (0, 1) by the increasing process $N(t) = \sup \{ n \in \mathbb{N} {\text{| }}M + nt > T_n \} $ and the random set I(x) = {n ε {0,..., N(t)}‖T _n -nt≦x<T _n+1 - nt}. The positions of shocks are given in a precise manner. We give the distribution of N(t) and also the distribution of its first jump. We also prove similar results when the initial value is u _μ(y, 0) = -μp(y/μ²) + μ^-1 max(y, 0), μ ε (0, 1).     

Exact results for two-dimensional coarsening

We consider the statistics of the areas enclosed by domain boundaries (‘hulls’) during the curvature-driven coarsening dynamics of a two-dimensional nonconserved scalar field from a disordered initial state. We show that the number of hulls per unit area, n _h (A, t)dA, with enclosed area in the range (A,A + dA), is described, for large time t, by the scaling form n _h (A, t) = 2c _h /(A + λ _h t)², demonstrating the validity of dynamical scaling in this system. Here $ c_h = {1 \mathord{\left/ {\vphantom {1 8}} \right. \kern-0em} 8}\pi \sqrt 3 $ is a universal constant associated with the enclosed area distribution of percolation hulls at the percolation threshold, and λ _h is a material parameter. The distribution of domain areas, n _d (A, t), is apparently very similar to that of hull areas up to very large values of A/λ _h t. Identical forms are obtained for coarsening from a critical initial state, but with c _h replaced by c _h /2. The similarity of the two distributions (of areas enclosed by hulls, and of domain areas) is accounted for by the smallness of c _h . By applying a ‘mean-field’ type of approximation we obtain the form n _d (A, t) ? 2c _d [λ _d (t+t ₀)] ^τ?2/[A+λ _d (t+t ₀)] ^τ , where t ₀ is a microscopic timescale and τ = 187/91 ? 2.055, for a disordered initial state, and a similar result for a critical initial state but with c _d → c _d /2 and τ → τ _c = 379/187 ? 2.027. We also find that c _d = c _h + O(c _h ² ) and λ _d = λ _h (1 + O(c _h )). These predictions are checked by extensive numerical simulations and found to be in good agreement with the data.     

Second moment of multiple-quantum NMR and a time-dependent growth of the number of multispin correlations in solids

The time evolution of multispin correlations (the growth of the number of correlated spins as a function of time) can be observed directly using the multiple-quantum nuclear magnetic resonance spectroscopy of solids. A quantity related to this number, namely, the second moment 〈n ²(t)〉 of the intensity distribution of coherences of different orders in the multiple-quantum spectrum can be calculated using the theory proposed in this work. An approach to the calculation of the four-spin time correlation function through which this moment is expressed is developed. The main sequences of contributions in the expansion of this function into a time power series are summed using the approximation of a large number of neighbors both for systems with a secular dipole-dipole interaction and for systems with a nonsecular effective interaction. An exponential dependence of 〈n ²(t)〉 is obtained. The value of 〈n ²(t)〉 is additionally calculated using an expansion in terms of orthogonal operators for three model examples corresponding to different limiting realizations of spin systems. It is shown that the results of the microscopic theory at least qualitatively agree with both the results obtained for model examples and experimental results obtained recently for adamantane.     

Determination of the protonic transference number for KH2PO4 by electromotive force measurements

The protonic transference number (t_H⁺) of KH₂PO₄ has been determined at 293 K as a function of hydrogen partial pressure (1>p_H2(atm)>10^-3) using EMF measurements. The results are consistent with earlier work which indicated that t_H⁺ is essentially unity (>0.97) for this material under the relevant experimental conditions.     

First passage time of multiple Brownian particles on networks with applications

In this article, we study some theoretical and technological problems with relation to multiple Brownian particles on networks. We are especially interested in the behavior of the first arriving Brownian particle when all the Brownian particles start out from the source s simultaneously and head to the destination h randomly. We analyze the first passage time (FPT) Y_sh(z) and the mean first passage time (MFPT) 〈Y_sh(z)〉 of multiple Brownian particles on complex networks. Equations of Y_sh(z) and 〈Y_sh(z)〉 are obtained. On a variety of commonly encountered networks, we observe first passage properties of multiple Brownian particles from different aspects. We find that 〈Y_sh(z)〉 drops substantially when particle number z increases at the first stage, and converges to d_sh, the distance between the source and the destination when z→∞. The distribution of FPT Prob{Y_sh(z)=t},t=0,1,2,… is also analyzed in these networks. The distribution curve peaks up towards t=d_sh when z increases. Consequently, if particle number z is set appropriately large, the first arriving Brownian particle will go along the shortest or near shortest paths between the source and the destination with high probability. Simulations confirm our analysis. Based on theoretical studies, we also investigate some practical problems using multiple Brownian particles, such as communication on P2P networks, optimal routing in small world networks, phenomenon of asymmetry in scale-free networks, information spreading in social networks, pervasion of viruses on the Internet, and so on. Our analytic and experimental results on multiple Brownian particles provide useful evidence for further understanding and properly tackling these problems.     

Lattice Dislocations in a 1-Dimensional Model

The spectral properties of the Schr?dinger operator T(t)=−d ²/dx ²+q(x,t) in L ²(ℝ) are studied, where the potential q is defined by q=p(x+t), x>0, and q=p(x), x<0; p is a 1-periodic potential and t∈ℝ is the dislocation parameter. For each t the absolutely continuous spectrum σ _ac (T(t))=σ _ac (T(0)) consists of intervals, which are separated by the gaps γ _n (T(t))=γ _n (T(0))=(α _n ⁻,α _n ⁺), n≥1. We prove: in each gap γ _n ≠?, n≥ 1 there exist two unique “states” (an eigenvalue and a resonance) λ _n ^±(t) of the dislocation operator, such that λ _n ^±(0)=α _n ^± and the point λ _n ^±(t) runs clockwise around the gap γ _n changing the energy sheet whenever it hits α _n ^±, making n/2 complete revolutions in unit time. On the first sheet λ _n ^±(t) is an eigenvalue and on the second sheet λ _n ^±(t) is a resonance. In general, these motions are not monotonic. There exists a unique state λ₀(t) in the basic gap γ₀(T(t))=γ₀(T(0))=(−∞ ,α₀ ⁺). The asymptotics of λ _n ^±(t) as n→∞ is determined. Received: 5 April 1999 / Accepted: 3 March 2000     

π0 Multiplicities in π+;p interactions at 10.5 GeVc

Measurement of the π⁰ multiplicity cross sections are reported for n₀ ? 6, where n⁰ is the number of produced π⁰ particles, and for N ? 8, where N is the number of charged particles. The inclusive π⁰ cross section is 29 ± 3 mb. Values for the correlation parameters, 〈n₀〉 and 〈n₀(n₀ ? 1)〉², are also presented.     

Investigation of crystal structure and new ellipsometric properties of hexagonal CdS epilayers

High quality hexagonal CdS epilayer was grown on GaAs (1 1 1) substrates by the hot-wall epitaxy method. The crystal structure of the grown CdS epilayers was confirmed to be the hexagonal structure by X-ray diffraction pattern and scanning electron microscopy image. The optical properties of the hexagonal CdS epilayers were investigated in a wide photon energy range between 2.0 and 8.5 eV using spectroscopic ellipsometry (SE) at room temperature. The data obtained by SE were analyzed to find the critical points of the pseudodielectric function spectra, 〈?(E)〉 = 〈?₁(E)〉 + i〈?₂(E)〉, such as E₀, E_1A, E_1B, E^0′, F₁, and two E₂ structures. In addition, the second derivative spectra, d²?(E)/dE², of the pseudodielectric function of hexagonal CdS epilayers were numerically calculated to determine the critical structures. Four structures, such as E^0′F₁, and two E₂ structures, from 6.0 eV to 8.0 eV were observed, for the first time, at 300 K by ellipsometric measurements for the hexagonal CdS epilayers.