Assessment of the effectiveness of downward water sprays for mitigating gaseous chlorine releases in partially confined spaces

Water sprays are sometimes used as a means of mitigating accidental releases of chlorine gas. This paper gives results of a series of small-scale experimental field tests on the mitigation of chlorine gaseous releases (about 1kg/min) by various downward water sprays. The releases were from a cylinder of liquefied chlorine located in a storage shed. The shed could be configured to simulate confined and semi-confined installations used at public swimming pools. The water sprays were located in the shed. During these tests, different types of spray nozzles and storage configurations were tested under various atmospheric conditions, in order to select the best water spray. It was shown that the best chlorine downstream concentration reduction (factor 3-5 at 10m) was achieved with a flat fan water spray for the semi-confined configuration. Poor absorption in water was observed (<1%). The highest absorption (roughly 5%) was obtained with a fog water spray for the confined configuration. This is expected since chlorine is a low soluble gas. It has been evidenced for the confined configuration, that even if reduction of concentration has been observed (factor 2), downstream concentration remains very high (>10,000ppm), and above critical level of toxicity. Consequently, the use of water sprays in this case without additives to promote absorption seems to be inefficient.     

Propagation through the ocean's surface at shallow angles with a laser beam

Propagation through the ocean's surface at shallow angles with a laser has been successfully demonstrated experimentally in the ocean. A 6-mJ multipulse laser at a depth of 1.5 m in water with an attenuation coefficient of approximately 3.3 m(-1) was easily detected 600 m away on a sunlit day at an angle of 1 degree to the ocean's surface. The measured efficiency was 3.6 x 10(-2) (J/J)/sr (joules received per receiver steradian per joule transmitted). Statistical ray trace analysis and physical tank modeling produced equivalent efficiencies.     

Characterization of sorption sites on Pilayella littoralis and metal binding assessment using 113Cd and 27Al nuclear magnetic resonance

Metal interactions with the cellular structures of the marine alga Pilayella littoralis have been investigated to better understand how biomaterials sorb dissolved metals. Algae metal binding capacity at pH 5.0 was 2000, 850, 430, and 560 micromol g(-1) of dried material for Al(III), Cu(II), Cd(II), and Co(II), respectively. Binding site characterization was assessed by 1H and 13C nuclear magnetic resonance spectroscopy. Also, Fourier Transform Infrared spectroscopy (FTIR) provided some information about the types of functional groups that appear to be present in the algal material. The results suggested the presence of carboxylate, ether, amino, and hydroxyl groups. Investigation of metal competition for the alga binding sites was performed using 27Al and 113Cd NMR spectroscopy, which proved to be a valuable technique for Al and Cd sorption assessment. Aluminum and Cu were efficiently sorbed by the alga sites, and the binding affinity order of these metals was Al(III) > Cu(II) > Cd(II) > Co(II).     

CCR5 and HIV infection

Chemokines and chemokine receptors play a crucial role in the trafficking of leukocyte populations across the body, and are involved in the development of a large variety of human diseases. CCR5 is the main coreceptor used by macrophage (M)-tropic strains of human immunodeficiency virus type 1 (HIV-1) and HIV-2, which are responsible for viral transmission. CCR5 therefore plays an essential role in HIV pathogenesis. A number of inflammatory CC-chemokines, including MIP-1 alpha, MIP-1 beta, RANTES, MCP-2, and HCC-1[9-74] act as CCR5 agonists, while MCP-3 is a natural antagonist of the receptor. CCR5 is mainly expressed in memory T-cells, macrophages, and immature dendritic cells, and is upregulated by proinflammatory cytokines. It is coupled to the Gi class of heterotrimeric G-proteins, and inhibits cAMP production, stimulates Ca2+ release, and activates PI3-kinase and MAP kinases, as well as other tyrosine kinase cascades. A mutant allele of CCR5, CCR5 delta 32 is frequent in populations of European origin, and encodes a nonfunctional truncated protein that is not transported to the cell surface. Homozygotes for the delta 32 allele exhibit a strong, although incomplete, resistance to HIV infection, whereas heterozygotes display delayed progression to acquired immunodeficiency syndrome (AIDS). Many other alleles, affecting the primary structure of CCR5 or its promoter have been described, some of which lead to nonfunctional receptors or otherwise influence AIDS progression. CCR5 is considered as a drug target in the field of HIV, but also in a growing number of inflammatory diseases. Modified chemokines, monoclonal antibodies and small chemical antagonists, as well as a number of gene therapy approaches have been developed in this frame.     

Changes in crash risk following re-timing of traffic signal change intervals

More than I million motor vehicle crashes occur annually at signalized intersections in the USA. The principal method used to prevent crashes associated with routine changes in signal indications is employment of a traffic signal change interval--a brief yellow and all-red period that follows the green indication. No universal practice exists for selecting the duration of change intervals, and little is known about the influence of the duration of the change interval on crash risk. The purpose of this study was to estimate potential crash effects of modifying the duration of traffic signal change intervals to conform with values associated with a proposed recommended practice published by the Institute of Transportation Engineers. A sample of 122 intersections was identified and randomly assigned to experimental and control groups. Of 51 eligible experimental sites, 40 (78%) needed signal timing changes. For the 3-year period following implementation of signal timing changes, there was an 8% reduction in reportable crashes at experimental sites relative to those occurring at control sites (P = 0.08). For injury crashes, a 12% reduction at experimental sites relative to those occurring at control sites was found (P = 0.03). Pedestrian and bicycle crashes at experimental sites decreased 37% (P = 0.03) relative to controls. Given these results and the relatively low cost of re-timing traffic signals, modifying the duration of traffic signal change intervals to conform with values associated with the Institute of Transportation Engineers' proposed recommended practice should be strongly considered by transportation agencies to reduce the frequency of urban motor vehicle crashes.     

Pedestrian crashes in Washington,DC and Baltimore

Police crash reports were obtained for pedestrian-motor vehicle crashes in Washington, DC (N = 852) and Baltimore (N = 1234) for the year 1998. Reports were coded using procedures developed and applied in these two cities during the 1970s, including the determination of pedestrian crash type, primary precipitating factor, and culpability. Results indicated substantial differences between crash patterns observed during the 1970s and those observed during 1998. Midblock dart-dash crashes, which typically involve a precipitating factor or critical error by a child pedestrian, decreased (from 37% to 15% in Washington). Across all crashes in both cities, the number of drivers who made a critical error leading to the crash was nearly equivalent to the number of pedestrians who made a critical error. Overall, pedestrians were slightly more likely to be judged culpable (50% vs. 39%). Turning vehicle crashes, which typically involve a driver's failure to grant a pedestrian the right of way at a signalized intersection, increased (from 9% to 25% in Washington). Countermeasures to reduce the number of pedestrians hit by turning vehicles are discussed.     

Derivation of the visual contrast response function by maximizing information rate

A graph of neural output as a function of the logarithm of stimulus intensity often produces an S-shaped function, which is frequently modeled by the hyperbolic ratio equation. The response of neurons in early vision to stimuli of varying contrast is an important example of this. Here, the hyperbolic ratio equation with a response exponent of two is derived exactly by considering the balance between information rate and the neural costs of making that information available, where neural costs are a function of synaptic strength and spike rate. The maximal response and semisaturation constant of the neuron can be related to the stimulus ensemble and therefore shift accordingly to exhibit contrast gain control and normalization.     

Convergence of a Generalized SMO Algorithm for SVM Classifier Design

Convergence of a generalized version of the modified SMO algorithms given by Keerthi et al. for SVM classifier design is proved. The convergence results are also extended to modified SMO algorithms for solving -SVM classifier problems.     

Magnetic Suspension Array Technology: Controlled Synthesis and Screening in Microfluidic Networks

Information tagging and processing are vital in information‐intensive applications, e.g., telecommunication and high‐throughput drug screening. Magnetic suspension array technology may offer intrinsic advantages to screening applications by enabling high distinguishability, the ease of code generation, and the feasibility of fast code readout, though the practical applicability of magnetic suspension array technology remains hampered by the lack of quality administration of encoded microcarriers. Here, a logic‐controlled microfluidic system enabling controlled synthesis of magnetic suspension arrays in multiphase flow networks is realized. The smart and compact system offers a practical solution for the quality administration and screening of encoded magnetic microcarriers and addresses the universal need of process control for synthesis in microfluidic networks, i.e., on‐demand creation of droplet templates for high information capacity. The demonstration of magnetic suspension array technology enabled by magnetic in‐flow cytometry opens the avenue toward point‐of‐care multiplexed bead‐based assays, clinical diagnostics, and drug discovery.