A filtered Rayleigh scattering system is developed and applied to measure the mole fraction of methane in a methane-air swirl flow through a transparent conical quartz quarl. Light scattering from the location where the laser beam is incident on the surface of the quarl is orders of magnitudes larger than Rayleigh scattering from the gas mixture of interest. This diffusive scattering is suppressed using molecular absorption by an iodine cell and using spatial filtering by an optical aperture. Residual stray light accounted for up to 5% of the total signal and had to be removed for accurate measurements. The flow consisted of a nonpremixed mixture of methane and air in the central jet surrounded by a strong swirling air flow. Measurements were conducted at a height of 4 mm from the fuel tube's exit for six different conditions of the swirl flow to demonstrate the ability of the instrument to study the effects of swirl strength and fuel flow rate on the mixing process. By using a four-leg pulse stretcher to allow higher laser energies in the probe volume, large collection optics and a reference iodine cell to monitor laser wavelength variations, standard deviations of ∼0.006 in air and ∼0.012 in a laminar methane flow were achieved for mole fraction measurements.
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http://dx.doi.org/10.1364/AO.58.005575 | DOI Listing |
In this paper, we studied the diffusion characteristics and distribution patterns of gas leakage in soil from buried natural gas pipelines. The three-dimensional simulation model of buried natural gas pipeline leakage was established using Fluent software. Monitoring points of gas leakage mole fraction were set up at different locations, and the influence of buried depth and pressure factors on the mole fraction and diffusion of leaked gas was analyzed.
View Article and Find Full Text PDFSci Rep
December 2024
School of Chemical Engineering, Iran University of Science and Technology (IUST), Tehran, Iran.
Benzene separation from hydrocarbon mixtures is a challenge in the refining and petrochemical industries. The application of liquid-liquid extraction process using ionic liquids (I.Ls) is an option for this separation.
View Article and Find Full Text PDFJ Chromatogr A
December 2024
Department "Area Materno-Infantile" Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan Italy.
Gravitational Field-Flow Fractionation (GrFFF) is an elution-based method designed for the separation of particles ranging from a few micrometers up to approximately 100 μm in diameter. Separation occurs over time, with particles being fractionated based on size and other physico-chemical properties. GrFFF takes advantage of gravitational forces acting perpendicularly to a laminar flow in a thin channel.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Department of Medicinal Chemistry, Uppsala University, P.O. Box 547, 751 23, Uppsala, Sweden. Electronic address:
We have investigated the effect of length and chemical structure of phospholipid tails on the spontaneous formation of unilamellar liposomal vesicles in binary solute mixtures of cationic drug surfactant and zwitterionic phosphatidylcholine phospholipids. Binary drug surfactant-phospholipid mixtures with four different phospholipids with identical headgroups (two saturated phospholipids 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC, 14:0) and 1,2-Dipalmitoyl-sn-glycero-3-phosphocholine (DPPC, 16:0), and two unsaturated lipids 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC, 18:1) and 1,2-Dierucoyl-sn-Glycero-3-Phosphatidylcholine (DEPC, 22:1)) combined with two different tricyclic antidepressant drugs (amitriptyline hydrochloride (AMT) and doxepin hydrochloride (DXP)) have been investigated with small-angle neutron scattering (SANS) and cryo-transmission electron microscopy (cryo-TEM). We observe a conspicuous impact of phospholipid tail structure on both micelle-to-vesicle transition point and vesicle size.
View Article and Find Full Text PDFChemphyschem
December 2024
University of Ioannina, Chemistry, 45110, Ioannina, GREECE.
The solvation structure and dynamics of the thiocyanate anion at infinite dilution in mixed N, N-Dimethylformamide (DMF)-water liquid solvents was studied using classical molecular dynamics simulation techniques. The results obtained have indicated a preferential solvation of the thiocyanate anions by the water molecules, due to strong hydrogen bonding interactions between the anion and water molecules. A first hydration shell at short intermolecular distances is formed around the SCN- anion consisting mainly by water molecules, followed by a second shell consisting by both DMF and water molecules.
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