A time-course study of the transfer of immunoglobulin G from blood to tracheal and lacrimal secretions in young turkeys

Three-week-old turkeys were injected intravenously with Bordetella avium-specific immunoglobulin G (IgG), and absorbance readings were measured in blood, tracheal washings, and lacrimal secretions using an enzyme-linked immunosorbent assay at various time intervals. IgG was detected in tracheal and lacrimal secretions as early as 5 minutes after injection and peaked at 10 minutes after injection. Thereafter, IgG absorbance declined rapidly, reaching background levels by 24 hours. The absorbance readings of IgG in all three sites were comparable at all times from 10 minutes to 24 hours after administration. The results indicated that movement of IgG from blood to mucosal surfaces in turkeys occurs rapidly.     

Thermally induced convection in narrow channels II. Experimental results for refrigerant 113

Sudden heating of a fluid in a tube or narrow channel induces localized pressure gradients and transient flow which can significantly affect the heat transfer rate. Experiments with a long, pulse-heated tube containing refrigerant 113 produced induced flow as well as pressure oscillations. This paper presents experimental results, and analyses of the system.     

A correlation for heat transfer to superphysical helium in turbulent flow in small channels

This paper presents a new correlation for the deterioration in heat transfer to turbulent flows of helium, relative to standard constant property correlations. The correlating parameters are arrived at by analogy between the heat transfer process to a gas with high thermal expansion and that which takes place in the presence of gas injection through a porous wall, the idea having been originally proposed by Kruzhilin. The idea appears to be applicable to the ideal gas state as well as the supercritical state. Comparison with available experimental data is made. Not only is the correlation of the data good, but the actual injection equation may be used to predict deterioration by as much as an order of magnitude.     

Improving predictability of sediment-porewater partitioning models using trends observed with PCB-contaminated field sediments

More than 1900 sediment-water partitioning coefficients were measured for 58 polychlorinated biphenyl (PCB) congeners in 53 historically contaminated sediments collected from 10 urban and rural waterways in the United States and Canada. Freely dissolved porewater concentrations were determined using passive sampling with polyoxymethylene. Measured total organic carbon (TOC)/water partitioning coefficients, K(TOC), ranged from one to nearly three orders-of-magnitude higher than typical literature values based on spiking experiments and model predictions. Although total PCB concentrations ranged from 0.08 to 194 mg/kg, the more highly contaminated sediments showed only slightly lower K(TOC) values than less-contaminated sediments. No correlation was observed between log K(TOC) values and sediment TOC, black carbon (BC), or BC/TOC fractions (r(2) typically <0.1). Utilizing a two-carbon model incorporating anthropogenic BC did not improve predictions over a one-carbon TOC model. A comparison of models recently validated for field data showed that a coal-tar poly parameter linear-free energy relationship (PP-LFER) and a Raoult's Law model were successful at predicting average log K(TOC) values, without the need for any calibration or fitting (within a factor of 10 more than 90% of the time, and within a factor of 30 more than 99% of the time). Predictions were further improved by the introduction of a Weathering Factor (WF) that accounts for the relative depletion of lower molecular weight congeners due to weathering. Highly weathered sediments (with a WF near 1) tended to follow the coal-tar PP-LFER and Raoult's Law model the closest. Less-weathered sediments (with WF ? 1) sorbed less than predicted by these models. Noncalibrated WF inclusive coal-tar PP-LFER and Raoult's Law models performed as well or better than a quantitative-structure activity relationship (QSAR) model calibrated specifically to the data. These recommended partitioning models here can readily be used for all 209-PCB congeners.     

Ambient gas/particle partitioning. 1. Sorption mechanisms of apolar, polar, and ionizable organic compounds

There remain several ambiguities in the literature regarding the dominating sorption mechanisms involved in gas/particle partitioning, particularly for polar and ionizable compounds. The various hypothetical mechanisms would depend differently on relative humidity (RH) and the presence of various aerosol components. Thus, in order to resolve these ambiguities, here we measured the RH-dependency of gas/particle partitioning constants, K(ip), for four diverse aerosol samples and a large set of chemicals covering apolar, polar, and ionizable organic compounds. In addition, we also removed the water-soluble components from two ambient particle samples to study how their presence influences sorption behavior. The measured K(ip) values collectively indicate that a dual-phase sorption mechanism is occurring, in which organic compounds partition into a RH-independent water-insoluble organic matter phase and additionally into a RH-dependent mixed-aqueous phase. All K(ip) values could be successfully fitted to a RH-dependent dual-phase sorption model. The trends in K(ip) data further support findings that the sorption behavior of ambient aerosol samples is different from raw mineral surfaces and soot.     

Thermodynamics of single-phase one-dimensional fluid flow

Fluid flow processes in helium within the range 4–10 K and 10–100 N cm^?2 pressure are similar to those of ordinary fluids near their critical points. Three thermodynamic parameters, the Gruneisen parameter, isentropic compressibility, and velocity of sound, which are weakly non-catalytic near the critical point, are used to describe fluid flow processes in fluids in the near critical range. It is found that if temperature is not used as a variable in fluid state equation, flow profiles can be easily evaluated in a single-phase fluid region, including close to or transecting the transposed critical line.     

Predicting methyl tert-butyl ether, tert-butyl formate, and tert-butyl alcohol levels in the environment using the fugacity approach

Through its extensive use as a fuel oxygenate, methyl tert-butyl ether (MTBE) is found nearly ubiquitouslythroughout the environment. To better understand the environmental fate of MTBE, fugacity models are commonly used. However, models developed by the scientific community and by governmental bodies differ in their predictions of relative MTBE concentrations for relevant environmental compartments and of seasonal concentration variations; further, to date they have not considered the formation of transformation products. In this study, the sensitivity of predicted environmental concentrations of MTBE and its two major degradation products, tert-butyl formate (TBF) and tert-butyl alcohol (TBA), to all types of model input parameters is analyzed in a probabilistic sensitivity analysis. This analysis allowed for an assessment of the most influential parameters for predicting soil, water, and air concentrations and thereby provided insight into why previous modeling studies on MTBE differed. Further, the information from the sensitivity analysis was used to parametrize a multispecies transformation model for predicting European concentration levels of MTBE and, for the first time, TBF and TBA. Water and air concentrations of MTBE predicted with the transformation model were in good agreement with measurements of environmental samples. No studies are available on environmental TBF and TBA levels to compare with model predictions; however, the modeling results indicate that, in the water phase, TBA concentrations may reach appreciable levels. One major uncertainty identified regarding the prediction of TBA levels was the fraction of TBA formed from atmospheric MTBE and TBF.     

A correlation of thermal conductivity data for helium

A correlation for the thermal conductivity of helium has been developed which covers the temperature range from temperatures just above the lambda line to 830 K, and densities up to about 160 kg m⁻³. The data used incorporate some recent experimental results which cover the temperature range from 4 K to 20 K including the critical region. The correlation gives an equation which generally fits the experimental data within ± 5%. However, at low temperature, the experimental data deviate up to about 10% from predictions based upon viscosity measurements or molecular dynamics calculations.     

Ultraviolet radiometry with synchrotron radiation and cryogenic radiometry

The combination of a cryogenic radiometer and synchrotron radiation enables detector scale realization in spectral regions that are otherwise difficult to access. Cryogenic radiometry is the most accurate primary detector-based standard available to date, and synchrotron radiation gives a unique broadband and continuous spectrum that extends from x ray to far IR. We describe a new cryogenic radiometer-based UV radiometry facility at the Synchrotron Ultraviolet Radiation Facility II at the National Institute of Standards and Technology. The facility is designed to perform a variety of detector and optical materials characterizations. The facility combines a high-throughput, normal incidence monochromator with an absolute cryogenic radiometer optimized for UV measurements to provide absolute radiometric measurements in the spectral range from 125 nm to approximately 320 nm. We discuss results on photodetector characterizations, including absolute spectroradiometric calibration, spatial responsivity mapping, spectroreflectance, and internal quantum efficiency. In addition, such characterizations are used to study UV radiation damage in photodetectors that can shed light on the mechanism of the damage process. Examples are also given for UV optical materials characterization.