用于无创血糖检测的光声池设计与研究

基于光声光谱的无创血糖监测方法具有灵敏度高、特异性好等突出优势,其光声池发挥着至关重要的作用,主要表现在如何提供一个优越的光声转换环境和增强光声信号的作用。现主要以RG理论为基础,分别对两种光声池进行设计和研究,给出光声池的设计方法及其结构参数计算过程,并通过具体实验来检验光声池结构参数设计的正确性、实用性和可行性。这两种光声池一种是非共振双腔差分光声池,适用于固体检测;另一种是非共振单腔光声池,适用于固液体样品检测。     

Differential photoacoustic cell for electrochemical and dynamic process with temperature control

A novel differential photoacoustic cell (DPC) for the study of dynamical processes has been developed. The DPC has the capability to measure in real time the amplitude and phase signals for the reference and the sample under study. The simultaneous measurement of both signals eliminates the instrumental function, and the presence of noise, due to any deviation originated by electrical, optical, and environmental factors. The DPC can be used at different temperature profiles in order to obtain the instrumental function IF(t,T). The DPC also has all the elements of an electrochemical cell capable of following the electrochemical processes. As a result of this new instrumentation it is possible to obtain in real time the amplitude and phase signals coming from the sample without any interference from the system and the viability to monitor in situ electrochemical and thermal processes. Two cases are presented as an illustrative demonstration of work fields: the electrodeposition of zinc on a steel substrate as well as the study of water and calcium ion diffusion into organic layers.     

Design and characteristics of a cell for photoacoustic spectroscopy of condensed matter

We describe a photoacoustic cell which is simple to use, easy to construct, and which gives a great sensitivity, expressed as a signal-to-noise ratio of 3000. Calibration of the cell indicates that it can be used with confidence as a general purpose photoacoustic cell.     

Adsorption from solutions in a centrifugal field and a device for studying it

A device is proposed for studying adsorption in a centrifugal field. Using this device, it is possible to introduce a sorbent into a reactor with an adsorbate directly during centrifugation. The device is composed of a dispenser built into the reactor lid and a command/reception system with an IR communication channel. The dispenser contains a hopper for loose material with a bottom door and a locking mechanism that keeps the door closed during centrifugation. In response to the command to unload the hopper, the reception part of the electronic circuit melts the thermoplastic thread that holds the rod and the hopper door at the bottom of the hopper, and the sorbent falls into the reactor.     

New controlled environment vitrification system for cryo-transmission electron microscopy: design and application to surfactant solutions

A newly designed controlled environment vitrification system for cryo-transmission electron microscopy of vitrified samples (cryo TEM) is presented. It significantly reduces the lag-time from blotting to vitrification by means of an optimized blotting procedure. Furthermore, a modified transfer system allows rapid transfer of the vitrified sample into the microscope and reduces the equilibration time. The practicable throughput of samples is thereby markedly increased. This new equipment is used to determine the overall size of individual polymer-like mixed lecithin–bile salt micelles, which very critically depends on the composition of the sample. The quantitative agreement with the results from independent light scattering experiments on the same sample supports the validity and performance of the presented sample preparation and handling procedures. In addition, these experiments demonstrate that cryo TEM experiments not only provide direct structural information, but furthermore permit a quantitative determination of micellar properties.     

A speckle-interferometric device for studying the cell biological activity

A modernized device intended for diagnosing the temperature-dependent activity of cells is described. The activity of cells was determined by finding the correlation coefficient of optical signals in speckle patterns recorded at different moments of time. It is shown that, as the temperature increases from 26 to 36°C, variations in the optical paths in cells increase from 16 to 26 nm. This is probably associated with the physiological activity of cells—trapping of large molecules or their conglomerates. In contrast to the previous variant of the device design, instead of a lipid membrane, a cell monolayer was used, which was cultivated on a plane-parallel glass plate. In order to reduce variations in the optical path lengths in a nutrient solution, a 1.7-mm-thick plane-parallel glass plate was additionally inserted into the cuvette. The modernization of the device also includes heating of the cuvette with hot air flows.     

Low temperature light microscopy and its application to study freezing in aqueous solutions and biological cell suspensions

The freezing of biological cell suspensions can be understood in terms of ice formation in the external suspension medium and the cellular reactions to the changing environment. Cryomicroscopy allows a quantitative analysis of both categories of phenomena. Besides freezing stages of appropriate thermal design, the components used for that purpose include a microcomputer (PSI 80) based control system, an image analysis system (Intellect 100) and a spectrophotometer (MPV compact). The investigation of extracellular ice formation is focused on the following effects: The redistribution of solutes in the residual liquid and the resulting concentration profiles are determined photometrically or densitometrically. The transitions between various morphologies of the ice–liquid phase boundary (planar–cellular–dendritic) can be related to interface instability theories. With respect to solute segregation, the studies also involve the formation of bubbles from supersaturated gaseous solutes and freezing potentials resulting from the differential incorporation of cations and anions into the solid phase. The interaction between particles or cells and the advancing ice front is determined from critical interface velocities marking the transition between repulsion and entrapment. The effects of freezing on biological cells are studied mainly with blood cells, especially lymphocytes. The water efflux due to osmotical gradients across the membrane yields volume shrinkage curves which are recorded and analysed from video images for various cooling rates. Beyond a certain threshold cooling rate, intracellular ice starts to form, and different crystallization morphologies can be detected. The intracellular crystallization temperatures depend on cooling and warming rates as well as on the presence of penetrating cryoadditives. A fluorescence viability is used to determine the percentage of damaged cells immediately after thawing.     

Electron microscopy of frozen water and aqueous solutions

Thin layers of pure water or aqueous solutions are frozen in the vitreous state or with the water phase in the form of hexagonal or cubic crystals, either by using a spray-freezing method or by spreading the liquid on alkylamine treated films. The specimens are observed in a conventional and in a scanning transmission electron microscope at temperatures down to 25 K. In general, the formation of crystals and segregation of solutes during freezing, devitrification and evaporation upon warming, take place as foreseen by previous X-ray, thermal, optical and electron microscopical studies. Electron beam damage appears in three forms. The devitrification of vitreous ice. The slow loss of material for the specimen at a rate of about one molecule of pure water for every sixty electrons. The bubbling in solutions of organic material for doses in the range of thousands of e nm^?2. We propose a possible model for the mechanism of beam damage in aqueous solutions. The structural and thermal properties of pure frozen water important for electron microscopy are summarized in an appendix.     

A unidirectional temperature gradient stage for solidification studies in aqueous solutions

A low temperature light microscope stage has been designed and fabricated for quantitative analysis of the solidification of aqueous solutions. Thermal boundary conditions are controlled during freezing so as to enable direct comparison of data with complementary theoretical models. Evolution of the temperature distribution within the system is monitored by a one-dimensional thermocouple array, and growth of the phase interface is measured via a displacement transducer. The two-dimensional solution concentration field is assessed by computer densitometric analysis of the grey scale distribution for a light absorbing solute. Experimental and theoretical analyses of freezing processes with the stage correlate well, and the data base is shown to be internally consistent by independent thermal and mechanical measures of the interface velocity.     

New instrument for measuring contact resistance developed for studying electrical contact phenomena

A new experimental apparatus for measuring the electrical contact resistance is described. This apparatus is essentially a conventional balance, modified for the examination of electrical contact resistance changes of silver and some other metal specimens due to increases and decreases in load and current.The results obtained show that plastic deformation takes place at the contact spots in response to an initial increase in load and elastic deformation occurs on a subsequent decrease in load. When a pair of Nichrome rods, which have a much higher resistivity than the silver specimen, are brought into contact with each other, the areas of the contact spots appear to be larger than those calculated. A fritting phenomenon, first studied in detail by Holm, occurred on the contact surfaces of the rods when they were subjected to heat and oxidation in the course of the experiment.     

LARM PKM solutions for torso design in humanoid robots

Human-like torso features are essential in humanoid robots. In this paper problems for design and operation of solutions for a robotic torso are discussed by referring to experiences and designs that have been developed at Laboratory of Robotics and Mechatronics (LARM) in Cassino, Italy. A new solution is presented with conceptual views as waist-trunk structure that makes a proper partition of the performance for walking and arm operations as sustained by a torso.     

Wireless device connection problems and design solutions

Users, especially the non-expert users, commonly experience problems when connecting multiple devices with interoperability. While studies on multiple device connections are mostly concentrated on spontaneous device association techniques with a focus on security aspects, the research on user interaction for device connection is still limited. More research into understanding people is needed for designers to devise usable techniques. This research applies the Research-through-Design method and studies the non-expert users’ interactions in establishing wireless connections between devices. The “Learning from Examples” concept is adopted to develop a study focus line by learning from the expert users’ interaction with devices. This focus line is then used for guiding researchers to explore the non-expert users’ difficulties at each stage of the focus line. Finally, the Research-through-Design approach is used to understand the users’ difficulties, gain insights to design problems and suggest usable solutions. When connecting a device, the user is required to manage not only the device's functionality but also the interaction between devices. Based on learning from failures, an important insight is found that the existing design approach to improve single-device interaction issues, such as improvements to graphical user interfaces or computer guidance, cannot help users to handle problems between multiple devices. This study finally proposes a desirable user-device interaction in which images of two devices function together with a system image to provide the user with feedback on the status of the connection, which allows them to infer any required actions.     

Simple setup for single and differential photoacoustic spectroscopy

Simple cells are described for normal and differential measurements in photoacoustic spectroscopy. The differential cell allows for easy background signal correction and for comparison of related samples. The arrangement allows great flexibility in cell design for adaptation to special sample forms. The normal cell can be used for very small volumes, liquids as well as solids, and is constructed in such a way as to allow the possibility of Helmholtz resonance to occur over a range of frequencies. The two cells are compared in terms of background and maximal signal strength and examples of spectra obtained with each of them are given. The general spectrometer setup is outlined as well.     

New large volume hydrothermal reaction cell for studying chemical processes under supercritical hydrothermal conditions using time-resolved in situ neutron diffraction

The design and testing of a new large volume Inconel pressure cell for the in situ study of supercritical hydrothermal syntheses using time-resolved neutron diffraction is introduced for the first time. The commissioning of this new cell is demonstrated by the measurement of the time-of-flight neutron diffraction pattern for TiO(2) (Anatase) in supercritical D(2)O on the POLARIS diffractometer at the United Kingdom's pulsed spallation neutron source, ISIS, Rutherford Appleton Laboratory. The sample can be studied over a wide range of temperatures (25-450 °C) and pressures (1-355 bar). This novel apparatus will now enable us to study the kinetics and mechanisms of chemical syntheses under extreme environments such as supercritical water, and in particular to study the crystallization of a variety of technologically important inorganic materials.     

燃料电池轿车车架设计

从燃料电池轿车车架的总体外形设计、车架结构、承载形式、车架材料、车架精确建模方法、车架设计中应满足的功能性和工艺性要求及车架分析计算等方面叙述了燃料电池轿车车架设计的方法和过程。     

The characean internodal cell as a model system for studying wound healing

This work describes the characean internodal cell as a model system for the study of wound healing and compares wounds induced by certain chemicals and UV irradiation with wounds occurring in the natural environment. We review the existing literature and define three types of wound response: (1) cortical window formation characterised by disassembly of microtubules, transient inhibition of actin-dependent cytoplasmic streaming and chloroplast detachment, (2) fibrillar wound walls characterised by exocytosis of vesicles carrying wall polysaccharides and membrane-bound cellulose synthase complexes coupled with endocytosis of surplus membrane and (3) amorphous, callose- and membrane-containing wound walls characterised by exocytosis of vesicles and endoplasmic reticulum cisternae in the absence of membrane recycling. We hypothesize that these three wound responses reflect the extent of damage, probably Ca(2+) influx, and that the secretion of Ca(2+) -loaded endoplasmic reticulum cisternae is an emergency reaction in case of severe Ca(2+) load. Microtubules are not required for wound healing but their disassembly could have a signalling function. Transient reorganisation of the actin cytoskeleton into a meshwork of randomly oriented filaments is required for the migration of wound wall forming organelles, just as occurs in tip-growing plant cells. New data presented in this study show that during the deposition of an amorphous wound wall numerous actin rings are present, which may indicate specific ion fluxes and/or a storage form for actin. In addition, we present new evidence for the exocytosis of FM1-43-stained organelles, putative endosomes, required for plasma membrane repair during wound healing. Finally, we show that quickly growing fibrillar wound walls, even when deposited in the absence of microtubules, have a highly ordered helical structure of consistent handedness comprised of cellulose microfibrils.     

Fracturing of melamine-embedded cells and tissues: a new technique for studying cell membranes

A new technique is presented for studying cell membranes by scanning electron microscopy. It is based on the observation that cells and tissues, embedded in a water-compatible melamine resin, are as hard as glass and consequently can be fractured with ease. Fracture faces so exposed are either sputter-coated for studying the surface topography or re-embedded for thin-sectioning, or both. Scanning electron microscopy shows that the fracture faces of a variety of tissues reveal cell membranes and associated structures with remarkable detail. Re-embedding and thin-sectioning of fractured frog retina, mycoplasma and red blood cells indicate that membranes become divided into their exo- and protoplasmic leaflets during fracturing. In this respect, the results reported here must be compared with conventional freeze-fracture techniques.     

New design for end grinding wheels

A new grinding-wheel design is developed by analysis of the nonuniform abrasive action in the case of plane grinding by the end of the wheel; the wheel parameters are established.