1,627 research outputs found
Finite Element Modelling of Bends and Creases during Folding Ultra Thin Stainless Steel Foils
Finite Element Modelling of an ultra thin foil of SUS 304 stainless steel is carried out. These foils are 20 mm and below in thickness. The development of stresses and strains during folding of these foils is studied. The objective of this study is to induce qualities of paper in the foils of stainless steel such that a public sculpture of origami can be built with the foil. Finite Element modelling of the fold, reverse fold, junctions of multiple folds as well as the finger-dents are carried out to quantify the extent of straining the steel foil would undergo while an object of origami is folded with it. It is important to know the extent of straining the foil would undergo during folding operation. With this knowledge, the through-thickness microstructure and microtexture can be studied which influence the fracture toughness and low cycle fatigue properties of the steel foil. The foil with the requisite qualities of paper can then be manufactured
Emission factors for open and domestic biomass burning for use in atmospheric models
Biomass burning (BB) is the second largest source of trace gases and the largest source of primary fine carbonaceous particles in the global troposphere. Many recent BB studies have provided new emission factor (EF) measurements. This is especially true for non-methane organic compounds (NMOC), which influence secondary organic aerosol (SOA) and ozone formation. New EF should improve regional to global BB emissions estimates and therefore, the input for atmospheric models. In this work we present an up-to-date, comprehensive tabulation of EF for known pyrogenic species based on measurements made in smoke that has cooled to ambient temperature, but not yet undergone significant photochemical processing. All EFs are converted to one standard form (g compound emitted per kg dry biomass burned) using the carbon mass balance method and they are categorized into 14 fuel or vegetation types. Biomass burning terminology is defined to promote consistency. We compile a large number of measurements of biomass consumption per unit area for important fire types and summarize several recent estimates of global biomass consumption by the major types of biomass burning. Post emission processes are discussed to provide a context for the emission factor concept within overall atmospheric chemistry and also highlight the potential for rapid changes relative to the scale of some models or remote sensing products. Recent work shows that individual biomass fires emit significantly more gas-phase NMOC than previously thought and that including additional NMOC can improve photochemical model performance. A detailed global estimate suggests that BB emits at least 400 Tg yr^(−1) of gas-phase NMOC, which is almost 3 times larger than most previous estimates. Selected recent results (e.g. measurements of HONO and the BB tracers HCN and CH_3CN) are highlighted and key areas requiring future research are briefly discussed
One-dimensional transport in polymer nanofibers
We report our transport studies in quasi one-dimensional (1D) conductors -
helical polyacetylene fibers doped with iodine and the data analysis for other
polymer single fibers and tubes. We found that at 30 K < T < 300 K the
conductance and the current-voltage characteristics follow the power law: G(T)
~ T^alpha with alpha ~ 2.2-7.2 and I(V) ~ V^betta with betta ~ 2-5.7. Both G(T)
and I(V) show the features characteristic of 1D systems such as Luttinger
liquid or Wigner crystal. The relationship between our results and theories for
tunneling in 1D systems is discussed.Comment: 11 pages, 3 figures, accepted for publication in Phys. Rev. Letter
Direct Observation of Site-specific Valence Electronic Structure at Interface: SiO2/Si Interface
Atom specific valence electronic structures at interface are elucidated
successfully using soft x-ray absorption and emission spectroscopy. In order to
demonstrate the versatility of this method, we investigated SiO2/Si interface
as a prototype and directly observed valence electronic states projected at the
particular atoms of the SiO2/Si interface; local electronic structure strongly
depends on the chemical states of each atom. In addition we compared the
experimental results with first-principle calculations, which quantitatively
revealed the interfacial properties in atomic-scale.Comment: 4 pages, 3 figure
Probing Spin-Charge Relation by Magnetoconductance in One-Dimensional Polymer Nanofibers
Polymer nanofibers are one-dimensional organic hydrocarbon systems containing
conducting polymers where the non-linear local excitations such as solitons,
polarons and bipolarons formed by the electron-phonon interaction were
predicted. Magnetoconductance (MC) can simultaneously probe both the spin and
charge of these mobile species and identify the effects of electron-electron
interactions on these nonlinear excitations. Here we report our observations of
a qualitatively different MC in polyacetylene (PA) and in polyaniline (PANI)
and polythiophene (PT) nanofibers. In PA the MC is essentially zero, but it is
present in PANI and PT. The universal scaling behavior and the zero (finite) MC
in PA (PANI and PT) nanofibers provide evidence of Coulomb interactions between
spinless charged solitons (interacting polarons which carry both spin and
charge)
Development of an intense positron source using a crystal--amorphous hybrid target for linear colliders
In a conventional positron source driven by a few GeV electron beam, a high
amount of heat is loaded into a positron converter target to generate intense
positrons required by linear colliders, and which would eventually damage the
converter target. A hybrid target, composed of a single crystal target as a
radiator of intense gamma--rays, and an amorphous converter target placed
downstream of the crystal, was proposed as a scheme which could overcome the
problem.This paper describes the development of an intense positron source with
the hybrid target. A series of experiments on positron generation with the
hybrid target has been carried out with a 8--GeV electron beam at the KEKB
linac. We observed that positron yield from the hybrid target increased when
the incident electron beam was aligned to the crystal axis and exceeded the one
from the conventional target with the converter target of the same thickness,
when its thickness is less than about 2 radiation length. The measurements in
the temperature rise of the amorphous converter target was successfully carried
out by use of thermocouples. These results lead to establishment to the
evaluation of the hybrid target as an intense positron source.Comment: 17pages, 10figure
K_L \ra \mu^\pm e^\mp \nu \overline{\nu} as background to K_L \ra \mu^\pm e^\mp
We consider the process K_L \ra \mu^\pm e^\mp \nu \overline{\nu} at next to
leading order in chiral perturbation theory. This process occurs in the
standard model at second order in the weak interaction and constitutes a
potential background in searches for new physics through the modes K_L \ra
\mu^\pm e^\mp. We find that the same cut, ~MeV, used to remove
the sequential decays K_{l3}\ra \pi_{l2} pushes the B(K_L \ra \mu^\pm e^\mp
\nu \overline{\nu}) to the level, effectively removing it as a
background.Comment: 8 pages, LaTeX, 1 figure appended as postscript file after
\end{document}. Fermilab-Pub-93/024-
The Fire INventory from NCAR (FINN): A High Resolution Global Model to Estimate the Emissions from Open Burning
The Fire INventory from NCAR version 1.0 (FINNv1) provides daily, 1 km resolution, global estimates of the trace gas and particle emissions from open burning of biomass, which includes wildfire, agricultural fires, and prescribed burning and does not include biofuel use and trash burning. Emission factors used in the calculations have been updated with recent data, particularly for the non-methane organic compounds (NMOC). The resulting global annual NMOC emission estimates are as much as a factor of 5 greater than some prior estimates. Chemical speciation profiles, necessary to allocate the total NMOC emission estimates to lumped species for use by chemical transport models, are provided for three widely used chemical mechanisms: SAPRC99, GEOS-CHEM, and MOZART-4. Using these profiles, FINNv1 also provides global estimates of key organic compounds, including formaldehyde and methanol. Uncertainties in the emissions estimates arise from several of the method steps. The use of fire hot spots, assumed area burned, land cover maps, biomass consumption estimates, and emission factors all introduce error into the model estimates. The uncertainty in the FINNv1 emission estimates are about a factor of two; but, the global estimates agree reasonably well with other global inventories of biomass burning emissions for CO, CO2, and other species with less variable emission factors. FINNv1 emission estimates have been developed specifically for modeling atmospheric chemistry and air quality in a consistent framework at scales from local to global. The product is unique because of the high temporal and spatial resolution, global coverage, and the number of species estimated. FINNv1 can be used for both hindcast and forecast or near-real time model applications and the results are being critically evaluated with models and observations whenever possible
Evolution of trace gases and particles emitted by a chaparral fire in California
Biomass burning (BB) is a major global source of trace gases and particles. Accurately representing the production and evolution of these emissions is an important goal for atmospheric chemical transport models. We measured a suite of gases and aerosols emitted from an 81 hectare prescribed fire in chaparral fuels on the central coast of California, US on 17 November 2009. We also measured physical and chemical changes that occurred in the isolated downwind plume in the first ~4 h after emission. The measurements were carried out onboard a Twin Otter aircraft outfitted with an airborne Fourier transform infrared spectrometer (AFTIR), aerosol mass spectrometer (AMS), single particle soot photometer (SP2), nephelometer, LiCor CO_2 analyzer, a chemiluminescence ozone instrument, and a wing-mounted meteorological probe. Our measurements included: CO_2; CO; NO_x; NH_3; non-methane organic compounds; organic aerosol (OA); inorganic aerosol (nitrate, ammonium, sulfate, and chloride); aerosol light scattering; refractory black carbon (rBC); and ambient temperature, relative humidity, barometric pressure, and three-dimensional wind velocity. The molar ratio of excess O_3 to excess CO in the plume (ΔO_3/ΔCO) increased from −5.13 (±1.13) × 10^(−3) to 10.2 (±2.16) × 10^(−2) in ~4.5 h following smoke emission. Excess acetic and formic acid (normalized to excess CO) increased by factors of 1.73 ± 0.43 and 7.34 ± 3.03 (respectively) over the same time since emission. Based on the rapid decay of C_2H_4 we infer an in-plume average OH concentration of 5.27 (±0.97) × 10^6 molec cm^(−3), consistent with previous studies showing elevated OH concentrations in biomass burning plumes. Ammonium, nitrate, and sulfate all increased over the course of 4 h. The observed ammonium increase was a factor of 3.90 ± 2.93 in about 4 h, but accounted for just ~36% of the gaseous ammonia lost on a molar basis. Some of the gas phase NH_3 loss may have been due to condensation on, or formation of, particles below the AMS detection range. NO_x was converted to PAN and particle nitrate with PAN production being about two times greater than production of observable nitrate in the first ~4 h following emission. The excess aerosol light scattering in the plume (normalized to excess CO_2) increased by a factor of 2.50 ± 0.74 over 4 h. The increase in light scattering was similar to that observed in an earlier study of a biomass burning plume in Mexico where significant secondary formation of OA closely tracked the increase in scattering. In the California plume, however, ΔOA/ΔCO_2 decreased sharply for the first hour and then increased slowly with a net decrease of ~20% over 4 h. The fraction of thickly coated rBC particles increased up to ~85% over the 4 h aging period. Decreasing OA accompanied by increased scattering/particle coating in initial aging may be due to a combination of particle coagulation and evaporation processes. Recondensation of species initially evaporated from the particles may have contributed to the subsequent slow rise in OA. We compare our results to observations from other plume aging studies and suggest that differences in environmental factors such as smoke concentration, oxidant concentration, actinic flux, and RH contribute significantly to the variation in plume evolution observations
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