Browsing by Author "Nguyen, Darien K."
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Item Biphasic Plasma Microreactor for Oxyfunctionalization of Liquid Hydrocarbons(Industrial & Engineering Chemistry Research, 2024-05-22) Nguyen, Darien K.; Cameli, Fabio; Dimitrakellis, Panagiotis; Vlachos, Dionisios G.Oxyfunctionalization of linear alkanes is important but challenging to achieve. Herein, we demonstrate a biphasic gas–liquid modular plasma microreactor utilizing Ar/O2 gas to selectively oxidize liquid n-dodecane (C12) in an electrified, catalyst-free fashion. C12 secondary alcohols and ketones are the major products, with selectivities of 45–60% and a maximum yield of 23%. Fine-tuning gas and liquid flow rates enhance the plasma–liquid interfacial area, leading to a conversion of >50%. Difunctional and oligomerized oxygenates, alongside lighter hydrocarbons stemming from carbon–carbon cleavage, form at higher conversions. The energy efficiency (0.189 μmol/J) of the modular microreactor is the highest reported among plasma systems. Alkane conversion can be further improved by increasing the length of the plasma region while maintaining excellent energy efficiencies. Similarly, sequential processing/recirculation can enhance the extent of the reaction. This system is also amenable to treating mixtures of liquid n-alkanes, where smaller hydrocarbons are oxidized preferentially to a certain extent. The vapor pressure and liquid temperature are the key parameters. The chemistry occurs primarily in the gas phase for the lighter hydrocarbons and switches to interfacial reactions for the larger ones.Item Oxidative Functionalization of Long-Chain Liquid Alkanes by Pulsed Plasma Discharges at Atmospheric Pressure(ACS Sustainable Chemistry and Engineering, 2022-11-17) Nguyen, Darien K.; Dimitrakellis, Panagiotis; Talley, Michael R.; O'Dea, Robert M.; Epps, Thomas H. III; Watson, Mary P.; Vlachos, Dionisios G.We introduce the oxidation of long aliphatic alkanes using non-thermal, atmospheric plasma processing as an eco-friendly route for organic synthesis. A pulsed dielectric barrier discharge in He/O2 gas mixtures was employed to functionalize n-octadecane. C18 secondary alcohols and ketones were the main products, with an optimal molar yield of ∼29.2%. Prolonged treatment resulted in the formation of dialcohols, diketones, and higher molecular weight oxygenates. Lighter hydrocarbon products and decarboxylation to CO2 were also observed at longer treatment times and higher power inputs. A maximum energy yield of 5.48 × 10–8 mol/J was achieved at short treatment times and high powers, associated with higher selectivity to primary oxygenates. Direct hydroxylation of alkyl radicals, as well as disproportionation reactions, are proposed as the main pathways to alcohols and ketones. The results hold promise for functionalizing long hydrocarbon molecules at ambient conditions using catalyst-free plasma discharges.Item Plasma-Enabled Ligand Removal for Improved Catalysis: Furfural Conversion on Pd/SiO2(ACS Nano, 2023-11-14) Nguyen, Darien K.; Vargheese,Vibin; Liao, Vinson; Dimitrakellis, Panagiotis; Sourav, Sagar; Zheng, Weiqing; Vlachos, Dionisios G.A nonthermal, atmospheric He/O2 plasma (NTAP) successfully removed polyvinylpyrrolidone (PVP) from Pd cubic nanoparticles supported on SiO2 quickly and controllably. Transmission electron microscopy (TEM) revealed that the shape and size of Pd nanoparticles remain intact during plasma treatment, unlike mild calcination, which causes sintering and polycrystallinity. Using Fourier transform infrared (FTIR) spectroscopy and X-ray photoelectron spectroscopy (XPS), we demonstrate the quantitative estimation of the PVP plasma removal rate and control of the nanoparticle synthesis. First-principles calculations of the XPS and CO FTIR spectra elucidate electron transfer from the ligand to the metal and allow for estimates of ligand coverages. Reactivity testing indicated that PVP surface crowding inhibits furfural conversion but does not alter furfural selectivity. Overall, the data demonstrate NTAP as a more efficient method than traditional calcination for organic ligand removal in nanoparticle synthesis.Item Theoretical insights into the adsorption and gas sensing performance of Fe/Cu-adsorbed graphene(Physical Chemistry Chemical Physics, 2024-04-17) Nguyen, Darien K.; Ho, Dai Q.; Trung, Nguyen TienThe binding mechanism of gas molecules on material surfaces is essential for understanding adsorption and sensing performance. In the present study, we examine the interaction of some volatile organic compounds (VOCs), including HCHO, C2H5OH, and CH3COCH3, on pristine graphene and its Fe/Cu-adsorbed surfaces using first-principles calculations. The results indicate that the adsorption of these molecules on graphene is regarded as physisorption, while chemisorption is observed for Fe/Cu attached surfaces. The binding of sites on molecules and surfaces primarily involves hydrogen bonds for the pure form of graphene. In contrast, stable interactions occur at functional groups such as >C[double bond, length as m-dash]O, –OH with Fe/Cu atoms, as well as C[double bond, length as m-dash]C bonds of π-rings on modified structures of graphene. It is noticeable that stronger adsorption is observed in the case of Fe addition (Gr-Fe) compared to Cu (Gr-Cu), enhancing the gas adsorption and sensing performance on graphene. Remarkably, the graphene surfaces supported by Fe and Cu improved selectivity in detecting VOC molecules, particularly C2H5OH and CH3COCH3 for Gr-Fe, and HCHO for Gr-Cu. Quantum chemical analyses reveal that the Fe/Cu⋯O/C contacts are covalent interactions, contributing significantly to the stability of configurations and sensing properties of Fe/Cu-adsorbed graphene. In summary, the observed improvements in selectivity, enhanced adsorption strength, and the identification of crucial interactions at the surface offer valuable insights into designing highly efficient gas sensors and developing advanced sensing materials.