Detection of subfemtosecond transients by means of nonlinear Raman scattering

Ultrafast transient processes are shown to qualitatively modify the nonlinear-optical response of a Raman-active medium. Fast processes with phase relaxation times shorter than the laser field cycle T ₀ = 2π/ω, where ω is the carrier frequency of the laser field, can be detected via modulation of the dipole moment at the frequency 2ω. This modulation is observed in the nonlinear-optical response of the medium against a background of a conventional, Raman part of the signal. Nonlinear Raman scattering can thus help to record ultrafast transients with a subcycle time resolution.     

Bound water fractions from quasi-elastic neutron scattering

Quasi-elastic neutron scattering measurements of AlCl₃ aqueous solution are analysed to derived the ratio of bound to solvent water molecules. We find that the ratio depends on the nature of the binding of the water molecules in the hydration shell and in the solvent. If the details of the binding are not known it is shown that such measurements must be carried out at small neutron wavevector transfers to obtain quantitative results.     

In-plane correlations in a polymer-supported lipid membrane measured by off-specular neutron scattering

Polymer-supported single lipid bilayers are models to study configurations of cell membranes. We used off-specular neutron scattering to quantify in-plane height-height correlations of interfacial fluctuations of such a lipid bilayer. As temperature decreased from 37 °C to 25 °C, the polymer swells and the polymer-supported lipid membrane deviates from its initially nearly planar structure. A correlation length characteristic of capillary waves changes from 30 μm at 37 °C to 11 μm at 25 °C, while the membrane bending rigidity remains roughly constant in this temperature range.     

Statistics of quantum beats in the time dependence of the neutron scattering

The numerical calculations of the delay time distributions for the neutron scattering have been carried out. The scattering of the short wave packet of neutrons with the broad energy interval 500–800 keV by ⁵⁸Ni nuclei has been studied. The decay curves and average times of the compound scattering were found as for the forward scattering as for the specific spin-parity states. The time oscillations of the decay curves were identified as quantum beats that were caused by the interference of the excited resonance set. The statistical analysis of the frequency spectra of the decay curves oscillations has been carried out. The behavior of the examined statistical observables turns out to be close to the Poisson law.     

Orientational correlations in molecular liquids by neutron scattering Carbon tetrachloride and germanium tetrabromide

Neutron diffraction structure factors for liquid carbon tetrachloride and germanium tetrabromide have been measured and are analysed to determine the molecular centre positional correlation function allowing for molecular angular correlation. The analysis shows quite unequivocally that appreciable molecular orientational correlations must exist in these liquids but that it may only extend to nearest neighbours. This is thought to cause the pair distribution function for the molecular liquids to be markedly different from that for atomic liquids such as argon and the difference is discussed.     

Uncovering flux line correlations in superconductors by reverse monte carlo refinement of neutron scattering data

We describe the use of reverse Monte Carlo refinement to extract structural information from angle-resolved data of a Bragg peak. Starting with small-angle neutron scattering data, the positional order of an ensemble of flux lines in superconducting Nb is revealed. We discuss the uncovered correlation functions in the light of topical theories, in particular, the "Bragg glass" paradigm.     

Abnormal state of pure neutron matter: Effects of correlations

We show that two different quasi classical approaches to abnormal states of dense nucleons give binding in pure neutron matter. Effects of short range correlations are found to increase the critical density.     

Effects of entanglement on the scattering intensity of neutron compton scattering by a proton pair in solids

We calculate scattering functions S(q-->,omega) of neutron Compton scattering (NCS) for a proton (deuteron) pair in the entangled state caused by the indistinguishability of particles. From the calculation, it is concluded that the effect of entanglement on the scattering intensity is undetectable in NCS experiments because of their high energy transfer and broad energy resolution.     

水泥老化过程中水动态的准弹性中子散射(QENS)谱分析

准弹性中子散射(quasi-elastic neutron scattering, QENS)实验是研究水泥老化过程中水动态的一种新颖的实验方法.本文利用老化时间分别为7, 14和30 d水泥样品的QENS谱实验数据, 通过应用四个高斯项的和的能量分辨函数R(Q, E)代替一个高斯项的能量分辨函数来改进经验扩散模型(empirical diffusion model, EDM), 再进行非线性最小二乘拟合.由此导出水泥样品中水动态的相关物理参数: 不动水数密度A, 自由水指数FWI=B₁/(A+B₁+B₂), 洛伦兹函数的半高宽Γ, 移动水跳跃之间的平均停留时间τ ₀及自扩散系数D_t, 而且可得出更为精准的QENS谱拟合曲线.拟合得到的物理参数可定量描述水泥老化过程中水动态过程, 从而为QENS实验在水泥老化过程中水动态研究的应用提供一种合理实用的谱分析方法.     

Diffusion of water in nano-porous polyamide membranes: Quasielastic neutron scattering study

Dynamics of water sorbed in a reverse osmosis polyamide membrane (ROPM) as studied by quasielastic neutron scattering (QENS) is reported here. The trimesoylchloride-m-phenylene diamine based ROPM is synthesized by interfacial polymerization technique. QENS data indicates that translational motion of water confined in ROPM gets modified compared to bulk water whereas rotational motion remains unaltered. Translational motion of water in ROPM is found to follow random jump diffusion with lower diffusivity compared to bulk water. Translational diffusivity does not show the Arrhenius behaviour.     

Structure of water in mesoporous organosilica by calorimetry and inelastic neutron scattering

In this paper, we describe the preparation of mesoporous organosilica samples with hydrophilic or hydrophobic organic functionality inside the silica channel. We synthesized mesoporous organosilica of identical pore sizes based on two different organic surface functionality namely hydrophobic (based on octyltriethoxysilane OTES) and hydrophilic (3-aminopropyltriethoxysilane ATES) and MCM-41 was used as a reference system. The structure of water/ice in those porous silica samples have been investigated over a range temperatures by differential scanning calorimetry (DSC) and inelastic neutron scattering (INS). INS study revealed that water confined in hydrophobic mesoporous organosilica shows vibrational behavior strongly different than bulk water. It consists of two states: water with strong and weak hydrogen bonds (with ratio 1:2.65, respectively), compared to ice-Ih. The corresponding O-O distances in these water states are 2.67 and 2.87 ?, which strongly differ compared to ice-Ih (2.76 ?). INS spectra for water in hydrophilic mesoporous organosilica ATES show behavior similar to bulk water, but with greater degree of disorder.     

Dynamics of supercooled confined water measured by deep inelastic neutron scattering

In this paper, we present the results of deep inelastic neutron scattering (DINS) measurements on supercooled water confined within the pores (average pore diameter ~ 20 Å) of a disordered hydrophilic silica matrix obtained through hydrolysis and polycondensation of the alkoxide precursor Tetra-Methyl-Ortho-Silicate via the sol-gel method. Experiments were performed at two temperatures (250 K and 210 K, i.e., before and after the putative liquid–liquid transition of supercooled confined water) on a “wet” sample with hydration h ~ 40% w/w, which is high enough to have water-filled pores but low enough to avoid water crystallization. A virtually “dry” sample at h ~ 7% was also investigated to measure the contribution of the silica matrix to the neutron scattering signal. As is well known, DINS measurements allow the determination of the mean kinetic energy and the momentum distribution of the hydrogen atoms in the system and therefore, allow researchers to probe the local structure of supercooled confined water. The main result obtained is that at 210 K the hydrogen mean kinetic energy is equal or even slightly higher than at 250 K. This is at odds with the predictions of a semiempirical harmonic model recently proposed to describe the temperature dependence of the kinetic energy of hydrogen in water. This is a new and very interesting result, which suggests that at 210 K, the water hydrogens experience a stiffer intermolecular potential than at 250 K. This is in agreement with the liquid–liquid transition hypothesis.     

补偿中子测井中与温度相关轻水热中子散射数据库的研制与应用

补偿中子测井受到环境温度的影响,利用数值模拟计算来进行修正,但目前的理论计算程序MCNP缺乏水的精细温度相关的热中子散射数据库。为了解决蒙特卡罗模拟热中子散射S(α,β)模型只能求解特定温度条件下中子输运问题的局限性,基于热中子散射的S(α,β)原理,采用内插法得到不同温度下水的频谱分布、振动;在最新的ENDFB-VII.1数据库上,利用NJOY99程序制作了ACE格式的轻水热中子散射截面数据库。利用系列次临界基准题对数据的准确性进行了验证,不同数据库之间的计算结果及基准题的结果符合得很好。自制的数据应用于测井仪器中的温度效应修正,取得了较好的效果。     

Dynamics of quantum correlations

The density matrix describing the state of a sybsystem of a physical system whose time dependence is assumed to follow a Schrödinger equation does not itself obey a von Neumann equation. The behavior of the eigenvalues and eigenfunctions of this density matrix is studied. An expression for the rate at which initially separating systems are de-separated is derived in perturbation theory. Indications are given that coherent photon states are more stable in the presence of charged particles than photon number eigenstates. The possible dynamical origin of super selection rules is discussed. A simple model is solved analytically.     

The correlation of molecular orientation in liquid water by neutron and X-ray scattering

The neutron diffraction structure factor for heavy water at 22°c has been measured for momentum transfers, ?Q, up to a Q of 13 å ^-1. The results have been interpreted by abstracting the molecular structure effects as far as possible and using models for the correlation of orientation of pairs of molecules ranging from completely uncorrelated orientation to that for adjacent molecules in ice I. Neither these nor any of the popular models for the structure of water, nor a non-hydrogen bonded model, fit the neutron diffraction data over the whole range of Q. Nevertheless, information about the molecular-centres structure factor is obtained, especially for Q up to about 3 å ^-1.

The method of analysis is generalized and applied to x-ray diffraction data and in particular to x-ray data for liquid water. It is shown that this method of analysis has some advantages over the conventional one. The effect of correlation of molecular orientation is less than that of molecular structure on x-ray scattering by water and rather more extensive information is obtained for the molecular-centres structure factor than from neutron data—if the conventional assumption of atomic electron clouds is accepted.

A comparison of the x-ray and neutron scattering data for liquid heavy water shows that the two sets of data are reasonably consistent for any of the usual models for water, except for the region of Q between 3 and 5 å ^-1. The molecular-centres structure factor of water has a weak double humped first maximum with peaks at 2·0 å ^-1 and 2·9å ^-1, probably followed by a damped oscillation. This contrasts with atomic liquids but is similar to that found in liquid carbon tetrachloride. The structure of liquid water is not, therefore, necessarily unique or unusual.     

Small angle neutron scattering study of two nonionic surfactants in water micellar solutions

Two classic nonionic surfactants — C₁₄E₇ (heptaethylene glycol monotetradecyl ether) and C₁₀E₇ (heptaethylene glycol monodecyl ether) were investigated in heavy water solution for concentration c = 0.17% (dilute regime) at different temperatures in the range t = 10–35°C by small angle neutron scattering (SANS) method. In the case of C₁₄E₇ surfactant — for all temperatures at c = 0.17% there are two axial ellipsoidal micelles with longer axis 15 nm at 10°C and 49.5 nm at 35°C in investigated solutions. For C₁₀E₇ surfactant at the same concentration of solution and temperature — two axial ellipsoidal micelles were observed, too. The longer axis is equal to 7.5 nm at 10°C, 9 nm at 20°C and at 35°C this axis is equal to 12 nm. Micelles of C₁₀E₇ nonionic surfactant are smaller than those of C₁₄E₇ surfactant in the same experimental conditions.