A tunable wedge‐shaped absorber for hard X‐ray synchrotron applications

The concept of a concave aluminium wedge‐shaped absorber for hard X‐ray synchrotron beamlines is presented. Unlike the commonly used absorber types (fixed‐thickness absorber sheets or binary exchangers of individual fixed absorbers), this concept allows a compact system, controlled with a single linear positioner, and provides a wide attenuation range as well as a precise tunability over a large energy range. Data were recorded at the Nanofocus Endstation of the MINAXS beamline, PETRA III, Hamburg, Germany.     

面向MEMS加速度传感器的仪表放大器的设计与实现

加速度传感器已经广泛应用于军事、工业、环境监测等领域，已经成为热点的研究对象，但是器件的小型化与可靠性成为限制该技术发展的重要瓶颈。因此，针对新型硅基MEMS 加速度传感器的信号处理电路小型化的问题，提出了一种与MEMS技术完全兼容基于CMOS工艺的片上集成运算放大器电路。通过提取分析相关加速度传感器的性能参数，设计低功耗、低噪声且符合精度等特殊要求的前置放大器。同时对集成仪表放大器的主要电路特性和功耗进行了仿真分析。从仿真结果看，设计的三运放仪表放大器的关键参数—共模抑制比可以到达101dB，整体性能良好。完成了对仿真结果的版图设计和验证，继而在华润上华0.5μm CMOS标准工艺线上进行了流片，完成了芯片的封装测试，该测试结果显示运放的增益能够达到42dB，功耗仅为5.25mW，符合预期的设计目标。     

Immersion cooling of silicon photomultipliers (SiPM) for nuclear medicine imaging applications

Silicon photomultipliers (SiPM) are compact, high amplification light detection devices that have recently been incorporated into magnetic field-compatible positron emission tomography (PET) scanners. To take full advantage of these devices, it is preferable to cool them below room temperature. Most current methods are limited to the cooling of individual detector modules, increasing complexity and cost of scanners made-up of a large number of modules. In this work we investigated a new method of cooling, immersion of the detector modules in non-electrically conductive, cooled liquid. A small-scale prototype system was constructed to cool a relatively large area SiPM-based, scintillator detector module by immersing it in a circulating bath of mineral oil. Testing demonstrated that the system rapidly decreased and stabilized the temperature of the device. Operation of the detector illustrated the expected benefits of cooling, with no apparent degradation of performance attributable to immersion in fluid.     

Electron temperature measurement in a surface-wave-produced argon plasma at intermediate pressures

The main objective of this work is to obtain the electron temperature in an argon surface-wave-produced plasma column at intermediate gas pressures. After proving that argon upper excited states remain in Excitation Saturation Balance, the value of electron temperature along the plasma column has been obtained using a modified Saha equation and a corrected Boltzmann-plot. Moreover, the electron energy distribution function has been verified to be nearly Maxwellian in a 0.8-2.8 torr intermediate pressure range. Received 24 July 2000 and Received in final form 19 January 2001     

Assay of Sodium and Potassium Activated Adenosine Triphosphatase in Submicrogram Fragments of Renal Tubules

Abstract

An improved method for measuring Na, K-ATPase in submicrogram fragments of single renal tubules approximately one millimeter long is described. The activity is determined by coupling ATP hydrolysis stoichiometrically to pyruvate kinase and the oxidation of NADH by lactic dehydrogenase. NADH oxidation is followed fluorimetrically using an instrument specially modified for increased sensitivity and stability.     

Summary of ISO/TC 201 Standard: ISO 18115‐1:2010 – surface chemical analysis – vocabulary – general terms and terms used in spectroscopy

This International Standard revises ISO 18115:2001 and the two subsequent amendments by bringing the material up to date and separating out the general terms and terms used in spectroscopy into Part 1, and terms relating to scanning probe microscopy into Part 2. This part, Part 1, covers 548 terms used in Auger electron spectroscopy, elastic peak electron spectroscopy, reflected electron energy loss spectroscopy, secondary ion mass spectrometry, ultra‐violet photoelectron spectroscopy, X‐ray photoelectron spectroscopy, and so on, as well as 52 acronyms. The terms cover words or phrases used in describing the samples, instruments, and theoretical concepts involved in surface chemical analysis. Copyright © 2012 Crown copyright.     

Radon contribution to single particle counts of the ARGO-YBJ detector

The ARGO-YBJ experiment is an air shower detector for gamma ray astronomy and cosmic ray studies with an energy threshold of ∼500 GeV. Working in “single particle mode”, i.e. counting the single particles hitting the detector at fixed time intervals, ARGO-YBJ can monitor cosmic ray and gamma ray transients at energies of a few GeV.The single particle counting rate is modulated by the atmospheric pressure and temperature, and is affected by the local radioactivity from soil and air. Among the radioactive elements, radon gas is of particular importance since its concentration in air can vary significantly, according to environmental conditions. In this paper we evaluate the contribution of the radon daughter gamma ray emitters to the single particle counting rate measured by ARGO-YBJ. According to our analysis, the radon gas contribution is roughly 1–2%, producing a counting rate modulation of the same order of magnitude of the atmospheric effects.     

Particle size characterization by quadruple-detector hydrodynamic chromatography

Particle size and shape and their distribution directly influence a variety of end-use material properties related to packing, mixing, and transport of powders, solutions, and suspensions. Many of the techniques currently employed for particle size characterization have found limited applicability for broadly polydisperse and/or nonspherical particles. Here, we introduce a quadruple-detector hydrodynamic chromatography (HDC) method utilizing static multiangle light scattering (MALS), quasi-elastic light scattering (QELS), differential viscometry (VISC), and differential refractometry (DRI), and apply the technique to characterizing a series of solid and hollow polystyrene latexes with diameters in the approximate range of 40–400 nm. Using HDC/MALS/QELS/VISC/DRI, we were able to determine a multiplicity of size parameters and their polydispersity and to monitor the size of the particles across the elution profile of each sample. Using self-similarity scaling relationships between the molar mass and the various particle radii, we were also able to ascertain the shape of the latexes and the shape constancy as a function of particle size. The particle shape for each latex was confirmed by the dimensionless ratio ρ ≡ R _G,z /R _H,z which, in addition, provided information on the structure (compactness) of the latexes as a function of particle size. Solid and hollow polystyrene latex samples were also differentiable using these methods. Extension of this method to nonspherical, fractal objects should be possible.       

Depolymerization study of sodium hyaluronate by flow field-flow fractionation/multiangle light scattering

Thermal depolymerization of ultrahigh-molecular-weight (UHMW) sodium hyaluronate (NaHA) was studied systematically by using frit-inlet asymmetrical flow field-flow fractionation/multiangle light scattering/differential refractive index (FI-AFlFFF/MALS/DRI). FI-AFlFFF was utilized for the size separation of NaHA samples which had been thermally degraded for varied treatment times, followed by light-scattering detection to determine MW and structural information of degraded NaHA products. Analysis of NaHA products showed time-dependent depolymerization of raw molecules into smaller-MW components, as well as unfolding of compact structures of UHMW NaHA. To determine whether the observed decrease in MW of sodium hyaluronate originated from the chain degradation of UHMW molecules or from dissociation of entangled complex particles that may have been formed by intermolecular association, narrow size fractions (1 × 10⁷–6 × 10⁷ and >6 × 10⁷ MW) of NaHA molecules were collected during FlFFF separation and followed by thermal treatment. Subsequent FI-AFlFFF/MALS analysis of collected fractions after thermal treatment suggested that the ultrahigh-MW region (>10⁷ Da) of NaHA is likely to result from supermolecular structures formed by aggregation of large molecules.     

Microfabricated planar glass gas chromatography with photoionization detection

We report the development of a microfabricated gas chromatography system suitable for the separation of volatile organic compounds (VOCs) and compatible with use as a portable measurement device. Hydrofluoric acid etching of 95 × 95 mm Schott B270 wafers has been used to give symmetrical hemi-spherical channels within a glass substrate. Two matching glass plates were subsequently cold bonded with the channels aligned; the flatness of the glass surfaces resulted in strong bonding through van der Waals forces. The device comprised gas fluidic interconnections, injection zone and 7.5 and 1.4 m long, 320 μm internal diameter capillaries. Optical microscopy confirmed the capillaries to have fully circular channel profiles. Direct column heating and cooling could be achieved using a combination of resistive heaters and Peltier devices. The low thermal conductivity of glass allowed for multiple uniform temperature zones to be achieved within a single glass chip. Temperature control over the range 10–200 °C was achieved with peak power demand of approximately 25 W. The 7.5 m capillary column was static coated with a 2 μm film of non-polar dimethylpolysiloxane stationary phase. A standard FID and a modified lightweight 100 mW photoionization detector (PID) were coupled to the column and performance tested with gas mixtures of monoaromatic and monoterpene species at the parts per million concentration level. The low power GC-PID device showed good performance for a small set of VOCs and sub ng detection sensitivity to monoaromatics.