Batikan Koroglu

Formation of 238U16O and 238U18O observed by time-resolved emission spectroscopy subsequent to laser ablation

We have measured vibronic emission spectra of an oxide of uranium formed after laser ablation of the metal in gaseous oxygen. Specifically, we have measured the time-dependent relative intensity of a band located at approximately 593.6 nm in 16O2. This band grew in intensity relative to neighboring atomic features as a function time in an oxygen environment but was relatively invariant with time in argon. In addition, we have measured the spectral shift of this band in an 18O2 atmosphere. Based on this shift, and by comparison with earlier results obtained from free-jet expansion and laser excitation, we can confirm that the oxide in question is UO, consistent with recent reports based on laser ablation in 16O2 only.We have measured vibronic emission spectra of an oxide of uranium formed after laser ablation of the metal in gaseous oxygen. Specifically, we have measured the time-dependent relative intensity of a band located at approximately 593.6 nm in 16O2. This band grew in intensity relative to neighboring atomic features as a function time in an oxygen environment but was relatively invariant with time in argon. In addition, we have measured the spectral shift of this band in an 18O2 atmosphere. Based on this shift, and by comparison with earlier results obtained from free-jet expansion and laser excitation, we can confirm that the oxide in question is UO, consistent with recent reports based on laser ablation in 16O2 only.

Shock Tube Ignition and CH4 Time-Histories during Propanal Oxidation

Propanal is an aldehyde intermediate formed during hydrocarbon combustion process. In this paper, we provide ignition delay time measurements behind reflected shock waves for stochiometric (Φ = 1) mixtures of propanal (CH3CH2CHO) and oxygen (O2) in argon bath gas at temperatures of 1100 < T < 1500 K and pressures around 1 atm. The measurements were conducted using the kinetics shock tube facility at UCF. The results were compared to data available in the literature as well as the predictions of three different aldehyde kinetic models. In addition, we used the laser absorption diagnostics for measuring methane (CH4) time-histories behind the reflected shock waves using a continuous wave distributed feedback interband cascade laser centered at 3403.4 nm. Methane concentration time histories were obtained for pyrolysis of propanal at 1300 K and around atmospheric pressures.

Plasma flow reactor for steady state monitoring of physical and chemical processes at high temperatures

We present the development of a steady state plasma flow reactor to investigate gas phase physical and chemical processes that occur at high temperature (1000 < T < 5000 K) and atmospheric pressure. The reactor consists of a glass tube that is attached to an inductively coupled argon plasma generator via an adaptor (ring flow injector). We have modeled the system using computational fluid dynamics simulations that are bounded by measured temperatures. In situ line-of-sight optical emission and absorption spectroscopy have been used to determine the structures and concentrations of molecules formed during rapid cooling of reactants after they pass through the plasma. Emission spectroscopy also enables us to determine the temperatures at which these dynamic processes occur. A sample collection probe inserted from the open end of the reactor is used to collect condensed materials and analyze them ex situ using electron microscopy. The preliminary results of two separate investigations involving the condensation of metal oxides and chemical kinetics of high-temperature gas reactions are discussed.

Gas Phase Chemical Evolution of Uranium, Aluminum, and Iron Oxides

We use a recently developed plasma-flow reactor to experimentally investigate the formation of oxide nanoparticles from gas phase metal atoms during oxidation, homogeneous nucleation, condensation, and agglomeration processes. Gas phase uranium, aluminum, and iron atoms were cooled from 5000 K to 1000 K over short-time scales (∆t < 30 ms) at atmospheric pressures in the presence of excess oxygen. In-situ emission spectroscopy is used to measure the variation in monoxide/atomic emission intensity ratios as a function of temperature and oxygen fugacity. Condensed oxide nanoparticles are collected inside the reactor for ex-situ analyses using scanning and transmission electron microscopy (SEM, TEM) to determine their structural compositions and sizes. A chemical kinetics model is also developed to describe the gas phase reactions of iron and aluminum metals. The resulting sizes and forms of the crystalline nanoparticles (FeO-wustite, eta-Al2O3, UO2, and alpha-UO3) depend on the thermodynamic properties, kinetically-limited gas phase chemical reactions, and local redox conditions. This work shows the nucleation and growth of metal oxide particles in rapidly-cooling gas is closely coupled to the kinetically-controlled chemical pathways for vapor-phase oxide formation.

Effects of Plume Hydrodynamics and Oxidation on the Composition of a Condensing Laser-Induced Plasma

High-temperature chemistry in laser ablation plumes leads to vapor-phase speciation, which can induce chemical fractionation during condensation. Using emission spectroscopy acquired after ablation of a SrZrO3 target, we have experimentally observed the formation of multiple molecular species (ZrO and SrO) as a function of time as the laser ablation plume evolves. Although the stable oxides SrO and ZrO2 are both refractory, we observed emission from the ZrO intermediate at earlier times than SrO. We deduced the time-scale of oxygen entrainment into the laser ablation plume using an 18O2 environment by observing the in-growth of Zr18O in the emission spectra relative to Zr16O, which was formed by reaction of Zr with 16O from the target itself. Using temporally resolved plume-imaging, we determined that ZrO formed more readily at early times, volumetrically in the plume, while SrO formed later in time, around the periphery. Using a simple temperature-dependent reaction model, we have illustrated that the formation sequence of these oxides subsequent to ablation is predictable to first order.