392 research outputs found
The thermal contact resistance of lubricant films in vacuum
This paper presents the results of an experimental investigation on the thermal contact resistance of lubricant films and bare interfaces. The apparatus and procedure used in the determination of these resistances are described. Twelve series of tests were performed to evaluate the effects of temperature and contact pressure on the thermal resistance of lubricant films. Variations of thermal contact resistance with temperature and contact pressure for four lubricants and for bare interfaces are presented graphically. The thermal resistances of the four lubricants tested in vacuum conditions: lithium grease, graphite grease, molykote grease, and silicone lubricant, were found to lie in the range from 0.0004 to 0.0035 hr sq ft F/Btu. The thermal resistances of the four lubricants in vacuum were lower than the thermal resistance for bare interfaces in air, and one order of magnitude lower than the thermal resistance of bare interfaces in vacuum. The molykote grease was least affected by temperature --Abstract, page ii
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Release of cholesterol-rich particles from the macrophage plasma membrane during movement of filopodia and lamellipodia.
Cultured mouse peritoneal macrophages release large numbers of ~30-nm cholesterol-rich particles. Here, we show that those particles represent fragments of the plasma membrane that are pulled away and left behind during the projection and retraction of filopodia and lamellipodia. Consistent with this finding, the particles are enriched in proteins found in focal adhesions, which attach macrophages to the substrate. The release of particles is abolished by blocking cell movement (either by depolymerizing actin with latrunculin A or by inhibiting myosin II with blebbistatin). Confocal microscopy and NanoSIMS imaging studies revealed that the plasma membrane-derived particles are enriched in 'accessible cholesterol' (a mobile pool of cholesterol detectable with the modified cytolysin ALO-D4) but not in sphingolipid-sequestered cholesterol [a pool detectable with ostreolysin A (OlyA)]. The discovery that macrophages release cholesterol-rich particles during cellular locomotion is likely relevant to cholesterol efflux and could contribute to extracellular cholesterol deposition in atherosclerotic plaques
A talin homologue of Dictyostelium rapidly assembles at the leading edge of cells in response to chemoattractant.
Black carbon over Mexico: the effect of atmospheric transport on mixing state, mass absorption cross-section, and BC/CO ratios
A single particle soot photometer (SP2) was operated on the NCAR C-130 during the MIRAGE campaign (part of MILAGRO), sampling black carbon (BC) over Mexico. The highest BC concentrations were measured over Mexico City (sometimes as much as 2 ÎĽg/m<sup>3</sup>) and over hill-fires to the south of the city. The age of plumes outside of Mexico City was determined using a combination of HYSPLIT trajectories, WRF-FLEXPART modeling and CMET balloon tracks. As expected, older, diluted air masses had lower BC concentrations. A comparison of carbon monoxide (CO) and BC suggests a CO background of around 65 ppbv, and a background-corrected BC/CO<sub>net</sub> ratio of 2.89&plusmn;0.89 (ng/m<sup>3</sup>-STP)/ppbv (average &plusmn; standard deviation). This ratio is similar for fresh emissions over Mexico City, as well as for aged airmasses. Comparison of light absorption measured with a particle soot absorption photometer (PSAP) and the SP2 BC suggests a BC mass-normalized absorption cross-section (MAC) of 10.9&plusmn;2.1 m<sup>2</sup>/g at 660 nm (or 13.1 m<sup>2</sup>/g @ 550 nm, assuming MAC is inversely dependent on wavelength). This appears independent of aging and similar to the expected absorption cross-section for aged BC, but values, particularly in fresh emissions, could be biased high due to instrument artifacts. SP2-derived BC coating indicators show a prominent thinly-coated BC mode over the Mexico City Metropolitan Area (MCMA), while older air masses show both thinly-coated and thickly-coated BC. Some 2-day-old plumes do not show a prominent thickly-coated BC mode, possibly due to preferential wet scavenging of the likely-hydrophilic thickly-coated BC
Cortical Factor Feedback Model for Cellular Locomotion and Cytofission
Eukaryotic cells can move spontaneously without being guided by external
cues. For such spontaneous movements, a variety of different modes have been
observed, including the amoeboid-like locomotion with protrusion of multiple
pseudopods, the keratocyte-like locomotion with a widely spread lamellipodium,
cell division with two daughter cells crawling in opposite directions, and
fragmentations of a cell to multiple pieces. Mutagenesis studies have revealed
that cells exhibit these modes depending on which genes are deficient,
suggesting that seemingly different modes are the manifestation of a common
mechanism to regulate cell motion. In this paper, we propose a hypothesis that
the positive feedback mechanism working through the inhomogeneous distribution
of regulatory proteins underlies this variety of cell locomotion and
cytofission. In this hypothesis, a set of regulatory proteins, which we call
cortical factors, suppress actin polymerization. These suppressing factors are
diluted at the extending front and accumulated at the retracting rear of cell,
which establishes a cellular polarity and enhances the cell motility, leading
to the further accumulation of cortical factors at the rear. Stochastic
simulation of cell movement shows that the positive feedback mechanism of
cortical factors stabilizes or destabilizes modes of movement and determines
the cell migration pattern. The model predicts that the pattern is selected by
changing the rate of formation of the actin-filament network or the threshold
to initiate the network formation
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