2014
DOI: 10.1063/1.4881679
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X-ray digital industrial radiography (DIR) for local liquid velocity (VLL) measurement in trickle bed reactors (TBRs): Validation of the technique

Abstract: Local liquid velocity measurements in Trickle Bed Reactors (TBRs) are one of the essential components in its hydrodynamic studies. These measurements are used to effectively determine a reactor's operating condition. This study was conducted to validate a newly developed technique that combines Digital Industrial Radiography (DIR) with Particle Tracking Velocimetry (PTV) to measure the Local Liquid Velocity (V(LL)) inside TBRs. Three millimeter-sized Expanded Polystyrene (EPS) beads were used as packing materi… Show more

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(1 citation statement)
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“…Intraocular tracing of miRNA/NP-BRZ C57/Bl6 mice, which were anesthetized by 5% chloral hydrate, were intravitreally injected with miRNA/NP-BRZ which was encapsulated along with a fluorescent tag, DIR (Mohd Salleh et al, 2014). Specific operations were performed as follows: 1) the conjunctiva was exposed using ophthalmic forceps; 2) Approximately, 3 ml of prepared miRNA/NP-BRZ with fluorescent tags was injected intravitreally by a 33 gauge needle into the back of ciliary body; 3) the eyeballs were removed at 6, 24, or 48 h after the operation, and fixed with 4% paraformaldehyde at 4 C overnight; 4) the eyeballs were soaked in 30% sucrose for 14 h at 4 C to cryoprotect them; 5) the eyeballs were then embedded into optimal cutting temperature (OCT) embedding medium (Sakura Finetek, Torrance, CA), frozen in liquid nitrogen and used for preparation of 6-mm-thick sections by cutting through optic nerve head; and 7) the images were acquired using a fluorescent microscope (DMI400B; Leica, Germany) with a 400Â objective lens.…”
Section: Drug Release and Kinetic Study In Vitromentioning
confidence: 99%
“…Intraocular tracing of miRNA/NP-BRZ C57/Bl6 mice, which were anesthetized by 5% chloral hydrate, were intravitreally injected with miRNA/NP-BRZ which was encapsulated along with a fluorescent tag, DIR (Mohd Salleh et al, 2014). Specific operations were performed as follows: 1) the conjunctiva was exposed using ophthalmic forceps; 2) Approximately, 3 ml of prepared miRNA/NP-BRZ with fluorescent tags was injected intravitreally by a 33 gauge needle into the back of ciliary body; 3) the eyeballs were removed at 6, 24, or 48 h after the operation, and fixed with 4% paraformaldehyde at 4 C overnight; 4) the eyeballs were soaked in 30% sucrose for 14 h at 4 C to cryoprotect them; 5) the eyeballs were then embedded into optimal cutting temperature (OCT) embedding medium (Sakura Finetek, Torrance, CA), frozen in liquid nitrogen and used for preparation of 6-mm-thick sections by cutting through optic nerve head; and 7) the images were acquired using a fluorescent microscope (DMI400B; Leica, Germany) with a 400Â objective lens.…”
Section: Drug Release and Kinetic Study In Vitromentioning
confidence: 99%