探讨降低电磁干扰之道

电磁干扰是电子设备和系统设计当中不能回避的问题.电源是把电子设备和电源网络联系起来的部分,因此电源引起的电磁干扰值得认真关注.随着开关稳压器的广泛使用,它越来越多地存在于电子设备中.目前,减轻电磁干扰的方法很多,包括接地、屏蔽和滤波等方式,本文将着重介绍用多相同步和扩展频谱频率调制(SSFM)的方式来降低电磁干扰.     

Effect of AlN and Al2O3 additions on the phase relationships and morphology of SiC Part I Compositions and properties

X-ray diffraction was utilized to follow the transformation from -SiC (3C) to the various -SiC polytypes in the presence of AlN and Al₂O₃ additives after hot pressing from 1700 to 2100°C. The 2H- and 6H-polytypes of -SiC were the predominate polytypes with additions of only AlN or Al₂O₃, respectively. The amount of 2H- and 6H-polytypes, and subsequently the microstructural morphology of the SiC materials, were found to be controlled by varying the amount of AlN and Al₂O₃. Improvements in fracture toughness to 9 MPa-m were achieved with flexural strengths ranging from 600 to 900 MPa. These results suggest that accurate control of the polytypic make-up of SiC-based materials, along with their mechanical properties, can be achieved through AlN and Al₂O₃ additions.     

Pathogenesis of oleic acid-induced lung injury in the rat: Distribution of oleic acid during injury and early endothelial cell changes

Oleic acid-induced lung injury, a well-described laboratory model for acute pulmonary injury in the rat and other species, causes morphologic and cellular changes similar to human adult respiratory distress syndrome (ARDS). Experiments were performed to test the hypothesis that the initial event of oleic acid lung injury is damage of the pulmonary vascular endothelium by oleic acid, with subsequent pulmonary damage and inflammation. Oleic acid levels were followed in the lung and other tissues by measuring accumulation of¹⁴C-oleic acid; the direct effects of oleic acid and other fatty acids on rat endothelial cells, alveolar type II cells, and hepatocytes in culture were determined. Lung tissue from treated rats was also examined by light and electron microscopy for evidence of endothelial cell damage. At 30 min after injury, oleic acid reached high concentrations in lung tissue as demonstrated by presence of radiolabel (3.24×10⁻⁶ moles per gram of tissue), with counts in the lung nearly an order of magnitude greater than in any other organ measured. Oleic acid was present in the lung mostly as free fatty acid (85%), and was also present in the alveolar fluid supernatans, rather than being cell-associated (1.7×10⁻⁷ moles vs. 1.1×10⁻⁸ moles at 30 min). Oleic acid was toxic to endothelial cells after one minute of exposure at concentrations of 5×10⁻⁴M and above. Electron microscopy showed endothelial cell changes as early as 10 min after induction of injuryin vivo, including the presence of endothelial cell blebbing. The results of these studies suggest that the initial event in oleic acid lung injury is damage to the pulmonary vascular endothelial cell.     

New words from old: A formalism for word-formation

Many languages make use of word-formation devices to allow speakers or writers to create new words when the existing vocabulary proves inadequate. In this paper we consider how these devices can be expressed formally, allowing them to be used in word- and sentence-generation, for dictionary expansion, and the like. The paper begins with some typical word-formation rules drawn mostly from French. Attention is drawn to some features of these rules which must be captured in any formal representation. The formal representation of a basic lexical transformation is presented in some detail, along with a number of examples. A computer implementation of the transformation system is described, together with a range of applications. A discussion of static and dynamic generation leads to the concept of an inverted transformation.Michael Levison is Professor and Head of the Department of Computing and Information Science at Queen's University at Kingston. His research interests currently centre on natural language generation and editing systems. He has written many articles on computer applications in literary and linguistic studies.Greg Lessard is an Associate Professor in the Department of French Studies at Queen's University. A linguist, his research interests include computational modelling of natural language performance (including second language learner French and linguistic humour) and computer-aided textual analysis (including repeated string and complex textual structures.)     

Optimal Time Bounds for Approximate Clustering

Clustering is a fundamental problem in unsupervised learning, and has been studied widely both as a problem of learning mixture models and as an optimization problem. In this paper, we study clustering with respect to the k-median objective function, a natural formulation of clustering in which we attempt to minimize the average distance to cluster centers. One of the main contributions of this paper is a simple but powerful sampling technique that we call successive sampling that could be of independent interest. We show that our sampling procedure can rapidly identify a small set of points (of size just O( $k \log \frac{n}{k}$ )) that summarize the input points for the purpose of clustering. Using successive sampling, we develop an algorithm for the k-median problem that runs in O(nk) time for a wide range of values of k and is guaranteed, with high probability, to return a solution with cost at most a constant factor times optimal. We also establish a lower bound of Ω(nk) on any randomized constant-factor approximation algorithm for the k-median problem that succeeds with even a negligible (say $\frac{1}{{100}}$ ) probability. The best previous upper bound for the problem was Õ(nk), where the Õ-notation hides polylogarithmic factors in n and k. The best previous lower bound of Ω(nk) applied only to deterministic k-median algorithms. While we focus our presentation on the k-median objective, all our upper bounds are valid for the k-means objective as well. In this context our algorithm compares favorably to the widely used k-means heuristic, which requires O(nk) time for just one iteration and provides no useful approximation guarantees.     

Electrochemical coding for multiplexed immunoassays of proteins

An electrochemical immunoassay protocol for the simultaneous measurements of proteins, based on the use of different inorganic nanocrystal tracers is described. The multiprotein electrical detection capability is coupled to the amplification feature of electrochemical stripping transduction (to yield fmol detection limits) and with an efficient magnetic separation (to minimize nonspecific adsorption effects). The multianalyte electrical sandwich immunoassay involves a dual binding event, based on antibodies linked to the nanocrystal tags and magnetic beads. Carbamate linkage is used for conjugating the hydroxyl-terminated nanocrystals with the secondary antibodies. Each biorecognition event yields a distinct voltammetric peak, whose position and size reflects the identity and level, respectively, of the corresponding antigen. The concept is demonstrated for a simultaneous immunoassay of beta(2)-microglobulin, IgG, bovine serum albumin, and C-reactive protein in connection with ZnS, CdS, PbS, and CuS colloidal crystals, respectively. These nanocrystal labels exhibit similar sensitivity. Such electrochemical coding could be readily multiplexed and scaled up in multiwell microtiter plates to allow simultaneous parallel detection of numerous proteins or samples and is expected to open new opportunities for protein diagnostics and biosecurity.     

Effects of fiber-optic probe design and probe-to-target distance on diffuse reflectance measurements of turbid media: an experimental and computational study at 337 nm

Fiber-optic probes are widely used in optical spectroscopy of biological tissues and other turbid media. Only limited information exists, however, on the ways in which the illumination-collection geometry and the overall probe design influence the interrogation of media. We have investigated both experimentally and computationally the effect of probe-to-target distance (PTD) on the diffuse reflectance collected from an isotropically (Lambertian) scattering target and an agar-based tissue phantom. Studies were conducted with three probes characterized by either common (single-fiber) or separate (two bifurcated multifiber probes) illumination and collection channels. This study demonstrates that PTD, probe design, and tissue scattering anisotropy influence the extent of the transport of light into the medium, the light-collection efficiency, and the sampling volume of collected light. The findings can be applied toward optimization of fiber-optic probe designs for quantitative optical spectroscopy of turbid media including biological tissues.     

Effect of ethanol on the growth of Clostridium botulinum

Model broth studies were carried out to investigate the effect of ethanol on the growth of proteolytic (group I) strains of Clostridium botulinum. Ethanol extended the pathogen's lag phase, decreased its exponential growth rate, and decreased its final level of growth in the stationary phase. In all cases, botulinum neurotoxin production was associated with growth. Micrographs of C. botulinum cultures grown at 37 degrees C in trypticase peptone glucose yeast extract (TPGY) broths containing 2 and 4% ethanol showed elongation of vegetative cells and interference with cell division. The inhibition of growth and toxin production at the ethanol level predicted (5.5%, wt/wt) was confirmed by microscopy and by the mouse bioassay. A subsequent study was carried out to determine the combined effect of ethanol (0 to 8% [wt/wt]), water activity (aw; 0.953 to 0.997), and pH (6.2 to 8.2) on the probability of the growth of and neurotoxin production by proteolytic strains of C. botulinum (10(3) spores per ml). Growth and neurotoxin production occurred in 1 to 3 days in TPGY broths without ethanol (0%) and in 2 to 4 days in broths containing 2% ethanol regardless of the aw or pH levels (P < 0.005). Growth and neurotoxin production were delayed by an ethanol concentration of 4% ethanol and completely inhibited by a concentration of 6%. At an ethanol concentration of 4%, the probability of growth and toxin production over 365 days (Pt) was influenced by aw and pH. After 365 days, the maximum probability of growth and toxin production (Pmax) was 1 for all but one combination. However, tau, the time it took for 50% of all eventually positive replicates for any given combination of barriers to show growth and/or turbidity, ranged from <3 to 229 days. All tubes of TPGY broths that showed no growth after 365 days were subcultured in fresh TPGY broths. In all cases, growth and toxin production occurred within 24 h at 37 degrees C, indicating the reversible (sporostatic and/or bacteriostatic) effect of ethanol on C. botulinum.