多体相互作用体系中的弛豫与扩散:一个尚未解决的问题

文章目的在于引起国内研究团体对一系列复杂相互作用体系中的弛豫和扩散的普适性进行关注.研究发现,无论是不同的化学结构（如无机物、有机物、聚合物、生物分子、胶体、金属和离子导电材料）,还是不同的物理状态（如晶态、玻璃态、液体、熔体、混合体系和含水系统）,以及不同的尺度（如从块体至纳米）,这种普适性无处不在 ［K.L.Ngai.Relaxation and Diffusion in Complex Systems.New York:Springer,2011］.该现象起源于多体系统的不可逆过程,取决于一些基本物理定律,与非简谐势引发的经典混沌有关.重新认识这种普适性不仅对众多不同领域的发展有利,而且能进一步弄清楚多体系统中的弛豫与扩散问题—— 一个重要而又未解决的物理问题.作者提出的耦合模型尽管不是一个严格而完整的答案,但却能够预测多体系统的弛豫和扩散特征,而且与实验结果吻合.基于该模型,绝大多数多体系统中的弛豫与扩散行为是相似的.该模型有望为这一难题的彻底解决奠定基石.     

On-line systems for continuous water and gas isotope ratio measurements

New continuous on-line techniques for water and air extracted from ice cores are developed. Water isotope ratio determination on any of the water phases (water vapour, water, ice) is of great relevance in different research fields, such as climate and paleoclimate studies, geological surveys, and hydrological studies. The conventional techniques for water isotopes are available in different layouts but all of them are rather time-consuming. Here we report new fast on-line techniques that process water as well as ice samples. The analysis time is only approximately 5 min per sample which includes equilibration and processing. Measurement precision and accuracy are better than 0.1 per thousand and 1 per thousand for delta18O and deltaD, respectively, comparable to conventional techniques. The new on-line techniques are able to analyze a wide range of aqueous samples. This allows, for the first time, to make continuous isotope measurements on ice cores. Similarly, continuous and fast analysis of aqueous samples can be of great value for hydrological, geological and perhaps medical applications.Furthermore, a new technique for the on-line analysis of air isotopes extracted from ice cores is developed. This technique allows rapid analyses with high resolution of the main air components nitrogen, oxygen, and argon. Measurement precision is comparable to precisions obtained by conventional techniques. It is now possible to measure delta15N and delta18O(atm) over entire ice cores helping to synchronize chronologies, to assess gas age-ice age differences, and to calibrate the paleothermometry for rapid temperature changes. This new on-line air extraction and analyzing technique complements the water methods in an ideal way as it separates the air from the melt-water of an ice sample. The remaining water waste flux can directly be analyzed by the water methods.     

Isolation of bicarbonate from equine urine for isotope ratio mass spectrometry

Sodium bicarbonate administration to horses prior to competition in order to enhance the buffer capacity of the organism is considered as a doping offence. The analysis of the isotopic composition of urinary bicarbonate/CO(2) (TCO(2)) may help to identify an exogenous bicarbonate source, as technical sodium bicarbonate exhibits elevated delta(13)C values compared with urinary total carbon. The isolation of TCO(2) from 60 equine urine samples as BaCO(3) followed by an isotopic analysis shows a significant variability of delta(13)C for TCO(2) of more than 10 per thousand. The delta(13)C of total carbon and TCO(2) seem to reflect different proportions of C3 and C4 plant material in the diet. The isotopic analysis of different mixtures of technical NaHCO(3) and equine urine shows that TCO(2) can be easily isolated without major isotopic fractionation; however, attention has to be paid to the storage time of urine samples, as a shift of delta(13)C of TCO(2) to lower values may occur.     

回旋电子束横纵速度比测试技术

摘要:通过对回旋电子束形成的电位和电场分布,推导出电子束横纵速度比测量的计算式.提出将电子束作传输线内导体等效,采用陶瓷电容分压器来测量速度比的方法.介绍了该测量装置的设计和加工工艺,及陶瓷电容分压器的标定方法和结果分析,并介绍了初步的原理性实验结果.该测试方法装置简单,测试电子束横纵速度比时不会破坏电子束的特性,能够...     

Stable isotope ratio method for the characterisation of the poultry house environment

Stable isotope analysis was applied to describe the poultry house environment. The poultry house indoor environment was selected for this study due to the relevant health problems in animals and their caretakers. Air quality parameters including temperature, relative humidity, airflow rate, NH₃, CO₂ and total suspended particles, as well as mean levels of total airborne bacteria and fungi count, were measured. Carbon isotope ratios (¹³C/¹²C) were obtained in size-segregated aerosol particles. The carbon (¹³C/¹²C) and nitrogen (¹⁵N/¹⁴N) isotope ratios were measured in feed, litter, scrapings from the ventilation system, feathers and eggs. Additionally, the distribution of δ¹³C and δ¹⁵N values in different tissues of the chicken was examined. The airborne bacteria and fungi extracted from the air filters collected from poultry farms were grown in the laboratory in media with known isotope values and measured for stable isotope ratios. Analysis of isotope fractionation between microorganisms and their media indicated the applicability of stable isotope analysis in bulk samples for the identification of source material. The analysed examples imply that stable isotope analysis can be used to examine the indoor environment along with its biology and ecology, and serve as an informative bioanalytical tool.     

回旋电子束横纵速度比测试技术

通过对回旋电子束形成的电位和电场分布,推导出电子束横纵速度比测量的计算式。提出将电子束作传输线内导体等效,采用陶瓷电容分压器来测量速度比的方法。介绍了该测量装置的设计和加工工艺,及陶瓷电容分压器的标定方法和结果分析,并介绍了初步的原理性实验结果。该测试方法装置简单,测试电子束横纵速度比时不会破坏电子束的特性,能够做到在回旋管运行时在线测量,实时监测电子束质量。     

Applications of cavity ring-down spectroscopy to high precision isotope ratio measurement of 13C/12C in carbon dioxide

Recent measurements of carbon isotopes in carbon dioxide using near-infrared, diode-laser-based cavity ring-down spectroscopy (CRDS) are presented. The CRDS system achieved good precision, often better than 0.2 per thousand, for 4% CO2 concentrations, and also achieved 0.15-0.25 per thousand precision in a 78 min measurement time with cryotrap-based pre-concentration of ambient CO2 concentrations (360 ppmv). These results were obtained with a CRDS system possessing a data rate of 40 ring-downs per second and a loss measurement of 4.0 x 10(-11) cm(-1) Hz(-1/2). Subsequently, the measurement time has been reduced to under 10 min. This standard of performance would enable a variety of high concentration (3-10%) isotopic measurements, such as medical human breath analysis or animal breath experiments. The extension of this ring-down to the 2 microm region would enable isotopic analysis at ambient concentrations, which, combined with the small size, robust design, and potential for frequent measurements at a remote site, make CRDS technology attractive for remote atmospheric measurement applications.     

High-resolution isotope shift measurement of the MgI 1 S 0 - 3 P 1 intercombination transition

We measured the isotope shift of the MgI intercombination line 3s3p ³ P ₁-3s ^{2 1} S ₀ (=457 nm) for the three stable isotopes ²⁴Mg, ²⁵Mg and ²⁶Mg. The measurement was performed by optical Ramsey spectroscopy (respectively saturation spectroscopy for ²⁵Mg) on a magnesium atomic beam. The rf precision of the measurement was achieved by using optical sideband techniques for the stabilization and tuning of a dye laser relative to an ultrastable cavity.     

New methods for fully automated isotope ratio determination from hydrogen at the natural abundance level

Abstract A variety of methods for measurement of (2)H/(1)H from H(2) are evaluated for their ability to be fully automated and for applicability to automated isotopic analysis of water and organic compounds. Equilibration of water with H(2) gas with the aid of a platinum catalyst has been commercialized into a fully automated sample preparation device. A second and newer technique, involving injecting water, methane, or other volatile organic compounds onto hot chromium in a reactor attached to the dual inlet system of a gas isotope ratio mass spectrometer, can be integrated with a conventional GC-autosampler to allow automated analysis of a variety of substrates. Both techniques result in precisions around 1‰ (δ notation) on the VSMOW scale, and are fast and accurate, and with appropriate mass spectrometers require only negligible scaling for the SLAP/VSMOW difference. Several experimental methods which show considerable promise employ "isotope ratio monitoring" (irm) inlet systems, in which a carrier gas is used for transport of H(2) to the mass spectrometer. Any such method has to address the problem of He ions corrupting the measurement of the H(2) ions. One such approach uses a heated palladium membrane for selective introduction of H(2) into the mass spectrometer, and a second involves modifications to the ion optics to control the stray helium ions. Both approaches have significant limitations that must be overcome before irm techniques can be used in routine applications, in particular for measuring hydrogen isotopes from GC effluents (irm-GCMS).     

一种空中辐射场测量用低轴比圆极化天线设计

在进行高功率微波(HPM)空中辐射场测量时,由于来波信号极化角度难以确定和受空中平台姿态影响等因素,普通线极化接收天线难以确保极化匹配,天线的极化失配会进一步降低辐射场参数测量的精确性。为了降低极化失配影响,在梯形微带圆极化单元天线分析设计的基础上,采用四阵元依次旋转90°和依次移相馈电的方式组建了一种低轴比微带圆极化阵列天线,该天线采用功分器和移相器作为馈电网络,天线在9.7 GHz实测增益约为9.4 dB,1 dB波束宽度约17.4°,轴比约0.4 dB。应用该圆极化天线可将极化失配引入的不确定度降低到0.2 dB以下,可满足高功率微波空中辐射场的精确测量需求。     

A new concept for sensitive in situ stable isotope ratio infrared spectroscopy based on sample modulation

Diode-laser absorption spectroscopy finds increasing applications in the emerging field of stable isotope research. To meet the requirements of the water isotopes measurement challenge in environmental research, ways have to be found to cope with the present limitations of spectroscopic systems. In this article, we discuss an approach based on the Stark effect in molecular spectra to reduce the influence of time-dependent, unwanted background structures generally superimposed on the desired signal from the spectral feature under investigation. A road map to high-sensitivity isotopic ratio measurements of water isotopes is presented. On the basis of an Allan Variance analysis of measured data, the detection limits have been calculated as a function of the integration time. To achieve the required optical density of about 6 x 10(-7) for H(2)(17)O measurements, the duty cycle has to be optimized and the implementation of a sample modulation within an optical multipass cell is a promising approach to increase the stability of spectroscopic instrumentation required for ecosystem research and airborne atmospheric platforms.     

A new concept for sensitive in situ stable isotope ratio infrared spectroscopy based on sample modulation

Diode-laser absorption spectroscopy finds increasing applications in the emerging field of stable isotope research. To meet the requirements of the water isotopes measurement challenge in environmental research, ways have to be found to cope with the present limitations of spectroscopic systems. In this article, we discuss an approach based on the Stark effect in molecular spectra to reduce the influence of time-dependent, unwanted background structures generally superimposed on the desired signal from the spectral feature under investigation. A road map to high-sensitivity isotopic ratio measurements of water isotopes is presented. On the basis of an Allan Variance analysis of measured data, the detection limits have been calculated as a function of the integration time. To achieve the required optical density of about 6×10^?7 for H₂ ¹⁷O measurements, the duty cycle has to be optimized and the implementation of a sample modulation within an optical multipass cell is a promising approach to increase the stability of spectroscopic instrumentation required for ecosystem research and airborne atmospheric platforms.     

Proposal for nonlinear refractive index measurement using spectral ratio in modulated OFRR dynamics

A novel method for measuring the nonlinear refractive index of an optical fiber using a spectral ratio between the modulation frequency and a harmonic component in a modulated optical fiber ring resonator (OFRR) is proposed. The spectral ratio between the modulation frequency and the 2nd-harmonics generated by phase-modulation through the OFRR is increased with increasing the input light power and has peaks above 5 W input power, however, the peaks was shifted to the lower input power below 1 W by averaging taken into account of the phase distribution. A experimental setup consisted of an OFRR system and an Ar-laser as a pump light source was used to determine the nonlinear refractive index of an optical fiber. In the experimental results, the peaks of the spectral ratio as a function of the input power was found out at 0.8 W and 0.45 W of the input power corresponding to the input source line at 488.0 nm and 514.5 nm, respectively. The profile was similar to that obtained by the simulation and the nonlinear refractive index of a optical fiber was determined as 1.0 × 10⁻²² m²/V² by a relationship between the input power giving the peak and the nonlinear refractive index.     

Evaluation of the performance of high temperature conversion reactors for compound-specific oxygen stable isotope analysis

In this study conversion conditions for oxygen gas chromatography high temperature conversion (HTC) isotope ratio mass spectrometry (IRMS) are characterised using qualitative mass spectrometry (IonTrap). It is shown that physical and chemical properties of a given reactor design impact HTC and thus the ability to accurately measure oxygen isotope ratios. Commercially available and custom-built tube-in-tube reactors were used to elucidate (i) by-product formation (carbon dioxide, water, small organic molecules), (ii) 2nd sources of oxygen (leakage, metal oxides, ceramic material), and (iii) required reactor conditions (conditioning, reduction, stability). The suitability of the available HTC approach for compound-specific isotope analysis of oxygen in volatile organic molecules like methyl tert-butyl ether is assessed. Main problems impeding accurate analysis are non-quantitative HTC and significant carbon dioxide by-product formation. An evaluation strategy combining mass spectrometric analysis of HTC products and IRMS ¹⁸O/¹⁶O monitoring for future method development is proposed.     

Branching ratio measurement of the decay K(L) --> e(+)e(-)mu(+)mu(-)

We have collected a 43 event sample of the decay K(L)-->e(+)e(-)mu(+)mu(-) with negligible backgrounds and measured its branching ratio to be (2.62+/-0.40+/-0.17)x10(-9). We see no evidence for CP violation in this decay. In addition, we set the 90% confidence upper limit on the combined branching ratios for the lepton flavor violating decays K(L)-->e(+/-)e(+/-)mu(-/+)mu(-/+) at B(K(L)-->e(+/-)e(+/-)mu(-/+)mu(-/+))< or =1.23x10(-10), assuming a uniform phase space distribution.