Catalysis and Reaction Engineering Commons^™

Preparation And Electrocatalytic Activity Of Nitrogen-Doping Tungsten Carbide Catalyst, Pian-Pian Yang, Li-Zhen Huang, Ying-Ying Li, Mei-Qin Shi, Chun-An Ma

Journal of Electrochemistry

Tungsten carbide (WC) is a promising electrocatalyst, however, its electrocatalytic activity is far inferior to Pt and Pt-group metal. In this work, nitrogen-doping tungsten carbide (WN|WC) catalysts with a nanoplate morphology were prepared via the tungsten nitride (WN) as the precursor and sodium tungstate as the tungsten source. The SEM and TEM results indicated that carbon atoms entered into the WN lattice to form the hexagonal close packed WC phase. In this way, an atomic scale heterostructure involving the closely linked interfaces between WN and WC was created . The XRD data confirmed that the cubic crystal structure of WN …

Nanoporous Carbon-Based Co2 Reduction Catalysts: Exploring The Combined Effects Of Surface Chemistry And Porosity, Wanlu Li

Dissertations, Theses, and Capstone Projects

For the first-time sulfur-doped, nitrogen-doped and sulfur, nitrogen-codoped nanoporous carbons were systematically studied as catalysts for CO₂ electrochemical reduction reaction (CO₂ERR). The Faradaic efficiencies (FE) of CO and CH₄ formation were calculated to evaluate the performance of these carbons. The best catalysts showed the FE of CO and CH₄ formation of 29% and 0.76%, respectively. It was found that the overall performance in CO₂ERR dramatically increased upon the reduction pretreatment of the carbons in N₂-saturated electrolyte before the CO₂ reduction process. The pretreated carbon showed the maximum FE of CO …

Title: Investigation Of Oxidative Reduction Reactions In Carbon-Based Electrocatalysts Presentation, Andrew Mason, Siamak Nejati, Shayan Kaviani

UCARE: Research Products

The expense of commonly used electrocatalysts such as Platinum and Palladium, make many battery technologies and electrochemical reactions cost-prohibitive. A new group of promising low-cost catalysts is doped carbon complexes. These materials need further development to reach the same activity as traditional catalysts. But by examining the Oxidative Reduction Reactions (ORR) of various carbon complexes, desirable characteristics and geometries can be identified and enhanced. For this comparative analysis, a series of Carbon Nanotube (CNT) and Graphene Complexes were tested.

NoX Formation In Light-Hydrocarbon, Premixed Flames, Robert T. Hughes

Theses and Dissertations--Mechanical and Aerospace Engineering

This study explores the reactions and related species of NO_x pollutants in methane flames in order to understand their production and consumption during the combustion process. To do this, several analytical simulations were run to explore the behavior of nitrogen species in the pre-flame, post- flame, and reaction layer regions. The results were then analyzed in order to identify all "steady-state" species in the flame as well as the determine all the unnecessary reactions and species that are not required to meet a defined accuracy. The reductions were then applied and proven to be viable.

Partial Oxidation Of Ethane To Acetic Acid Using A Metallic Pd Promoted Movnb Catalyst Supported On Titania, Sulaiman Al-Mayman, Abdulrhman S. Al-Awadi, Yousef S. Al-Zeghayer, Moustafa A. Soliman

Chemical Engineering

The partial oxidation of ethane to acetic acid on a multi-component Mo16V6.37Nb2.05Pdx oxide catalyst supported on Degussa P25 titania has been investigated. The catalyst was characterized using BET surface area, X ray diffractometer (XRD) and transmission electron microscopy (TEM). The reaction was carried out in a differential reactor in a temperature range of 200-275°C and at a total pressure of 200 psi. The addition of trace amounts of nano-palladium, either as palladium oxides or metallic palladium, enhanced ethane oxidation towards the formation of acetic acid with near-complete depletion of the ethylene intermediate from the reactor effluent. The introduction of nano-Pd …

Assembling Of Niox/Mwcnts-Gc Anodic Nanocatalyst For Water Electrolysis Applications, Islam M. Al-Akraa Dr., Yaser M. Asal Mr, Saher D. Khamis Eng

Chemical Engineering

Glassy carbon (GC) electrode is intended to be modified with nickel oxide (NiOx) and multiwalled carbon nanotubes (MWCNTs) in the anodic reaction of water electrolysis. NiOx deposition time is optimized and a 5 min was enough to attain the maximum activity. A further modification of the catalyst with MWCNTs could greatly enhance its stability during continuous electrolysis. As an outcome, an energy amount of 21.7 kWh/KgO2 is minimized. Several electrochemical and materials characterization setups will be utilized to test the catalyst activity and to know its geometry and structure.

Fabrication Of Cuox-Pd Nanocatalyst Supported On A Glassy Carbon Electrode For Enhanced Formic Acid Electro-Oxidation, Islam M. Al-Akraa Dr., Ahmad M. Mohammad Prof, Mohamed S. El-Deab Prof, Bahgat E. El-Anadouli Prof

Chemical Engineering

Formic acid (FA) electro-oxidation (FAO) was investigated at a binary catalyst composed of palladium nanoparticles (PdNPs) and copper oxide nanowires (CuOxNWs) and assembled onto a glassy carbon (GC) electrode. /e deposition sequence of PdNPs and CuOxNWs was properly adjusted in such a way that could improve the electrocatalytic activity and stability of the electrode toward FAO. Several techniques including cyclic voltammetry, chronoamperometry, field-emission scanning electron microscopy, energy dispersive X-ray spectroscopy, and X-ray diffraction were all combined to report the catalyst’s activity and to evaluate its morphology, composition, and structure. /e highest catalytic activity and stability were obtained at the CuOx/Pd/GC …

Surface And Structural Modification Of Carbon Electrodes For Electroanalysis And Electrochemical Conversion, Yan Zhang

Theses and Dissertations--Chemistry

Electrocatalysis is key to both sensitive electrochemical sensing and efficient electrochemical energy conversion. Despite high catalytic activity, traditional metal catalysts have poor stability, low selectivity, and high cost. Metal-free, carbon-based materials are emerging as alternatives to metal-based catalysts because of their attractive features including natural abundance, environmental friendliness, high electrical conductivity, and large surface area. Altering surface functionalities and heteroatom doping are effective ways to promote catalytic performance of carbon-based catalysts. The first chapter of this dissertation focuses on developing electrode modification methods for electrochemical sensing of biomolecules. After electrochemical pretreatment, glassy carbon demonstrates impressive figures-of-merit in detecting small, redox-active …

The Active Phase Of Gold Catalyst For Propylene Epoxidation, Manchhiben Patel

Summer Community of Scholars Posters (RCEU and HCR Combined Programs)

No abstract provided.

Reaction Kinetics Of The Hydrogenation Of Phenol In A Tubular Reactor, Michael Selzer

Williams Honors College, Honors Research Projects

The reaction kinetic parameters for the hydrogenation of phenol to cyclohexanone are determined for the liquid phase reaction with the palladium catalyst supported on an electrospun PVDF membrane. Runs of the reactor were completed at catalyst loadings of 40, 50, and 60 g/m², and tube diameters of 0.187 in and 0.25 in with a runtime of ten hours. One-dimensional and two-dimensional models of the experimental setup were developed. Fitting data to the one-dimensional model found that the pre-exponential factor was 2.50 x 10⁴, the activation energy was 7.69 kJ/mol, and the order with respect to phenol …

Graphene As A Solid-State Ligand For Palladium Catalyzed Cross-Coupling Reactions, Yuan Yang

Theses and Dissertations

Palladium-catalyzed carbon-carbon cross-coupling reactions have emerged a broadly useful, selective and widely applicable method to synthesize pharmaceutical active ingredients. As currently practiced in the pharmaceutical industry, homogeneous Pd catalysts are typically used in cross-coupling reactions. The rational development of heterogeneous catalysts for cross-coupling reactions is critical for overcoming the major drawbacks of homogeneous catalysis including difficulties in the separation, purification, and quality control process in drug production. In order to apply heterogeneous catalysis to flow reactors that may overcome this limitation, the catalyst must be strongly bound to a support, highly stable with respect to leaching, and highly active. While …

Reaction Kinetics Of Ethane Partial Oxidation To Acetic Acid, Sulaiman Al-Mayman, Moustafa A. Soliman, Abdulrhman S. Al-Awadi, Yousef S. Al-Zeghayer

Chemical Engineering

The partial oxidation of ethane to ethylene and acetic acid on supported MoVNbPd/TiO2 (P25 of Degussa) has been investigated. Pd was added in a nano-metallic form. The catalyst composition was also different from similar studied catalysts. This results in a better selectivity towards acetic acid formation. The reaction was carried out in a tubular reactor at temperature range 225–275 °C, total pressure range 0–200 psig and oxygen percentage in the feed gas of 10–40%. The feed gas contains ethane and oxygen. In this work, we develop a kinetic model for the reaction for the developed catalyst. In this model, we …

Fabrication Of Mnox/Mwcnts-Gc Nanocatalyst For Oxygen Evolution Reaction, Islam M. Al-Akraa Dr., Yaser M. Asal Mr, Amr M. Arafa Eng.

Chemical Engineering

Manganese oxide (MnOx) and multiwalled carbon nanotubes (MWCNTs) are intended to modify the GC electrode for oxygen evolution reaction (OER). Optimization of MnOx loading is carried out and the deposition of 55 cycles was sufficient to obtain the highest activity toward OER. The stability of the catalyst is enhanced by the addition of MWCNTs. As a result, an amount of 22 kWh/Kg of O2 of energy is saved. Several techniques including cyclic voltammetry, linear sweep voltammetry, chronoamperometry, chronopotentiometry, field-emission scanning electron microscopy, and energy dispersive X-ray spectroscopy will be combined to track the catalyst activity and to determine its morphology …

The Role Of Microenvironment Reagent Solubility On Reaction Kinetics Of 4-Nitrophenol Reduction, Michael P. Zeevi, Andrew Harrison, Christina Tang

UROP Posters

The Role of Microenvironment Reagent Solubility on Reaction Kinetics of 4-Nitrophenol Reduction

Michael Zeevi¹ with Andrew Harrison¹ and Christina Tang, PhD¹

¹Department of Chemical and Life Science Engineering, VCU School of Engineering

Introduction: Nanoparticles are of increasing interest due to their high surface area to volume ratio, as well as that they enable fine-tuning of the reaction microenvironment. Through flash nanoprecipitation, core-shell polymer nanoreactors were formed by directed self-assembly. Using the reduction of 4-nitrophenol as a model reduction reaction, we investigated the effect of reagent solubility in the nanoreactor microenvironment’s on nanoreactor kinetics.

Methods: The standard …

Electroactivities Of Pd/Fe3O4-C Catalysts For Electro-Oxidation Of Methanol, Ethanol And Propanol, Tao Zou, Qing-Feng Yi, Yuan-Yuan Zhang, Xiao-Ping Liu, Guo-Rong Xu, Hui-Dong Nie, Xiu-Lin Zhou

Journal of Electrochemistry

Development of palladium (Pd) catalysts with high electroactivity for alcohol oxidation is significant for alcohol fuel cells. In this work, Pd nanoparticles were formed by sodium borohydride (NaBH₄) reduction method and subsequently deposited on the surface of carbon supported ferriferrous oxide (Fe₃O₄/C) composites to obtain the Pd/Fe₃O₄-C catalysts with different Fe₃O₄ loadings. Their transmission electron microscopic (TEM) images show that the Pd nanoparticles were uniformly dispersed on the Fe₃O₄/C. Electroactivities of the prepared Pd/Fe₃O₄-C catalysts toward oxidations of C1-C3 …

Kinetics And Mechanism Toward Electrochemical Reductions Of Sodium Bromide And Methanol Over Iron Electrodes, Qun Liao, Shu-Feng Zhang, Wen-Hua Leng

Journal of Electrochemistry

It is of technological value and scientific interest to the electro-synthesis of ferrocene, conversion of carbon dioxide (CO₂) and organic electro-synthesis in non-aqueous solutions by investigating the kinetics and mechanism toward electrochemical reductions of sodium bromide (NaBr) and methanol over iron electrodes. However, few reports in the related researches are available. In this article, the kinetics and mechanism toward electrochemical reductions of NaBr and methanol over iron electrodes were examined in detail by carrying out the polarization curve and electrochemical impedance spectroscopic measurements. The results showed that methanol was the reactant, while Na⁺ ions were functioned only …

Cobalt-Based Nitrogen-Doped Carbon Non-Noble Metal Catalysts For Oxygen Reduction Reaction, Meng-Xiu Jiang, Jing Zhang, Yue-Hua Li, Rong Zhang

Journal of Electrochemistry

Transition metal-nitrogen co-doped carbon catalysts have attracted significant attention because of their reasonable activity and remarkable selectivity toward oxygen reduction reaction (ORR) as cathodic reaction in fuel cells. However, the role of transition metal in the active sites of the catalysts still is uncertain. In this work, the Co_x-N_y/C-T catalysts were prepared with BP2000 as a carbon source, urea (Ur) as a nitrogen source and Co(OAc)₂•4H₂O as a metal precursor by a simple chemical method. Meanwhile, in order to optimize the ORR activity, the catalysts were synthesized with different amounts of Co …

Core-Shell Pd@Pt Ultrathin Nanowires As Durable Oxygen Reduction Electrocatalysts, Xin Wang, Yun-Jie Xiong, Liang-Liang Zou, Qing-Hong Huang, Zhi-Qing Zou, Hui Yang

Journal of Electrochemistry

This paper describes a simple CO-assisted reduction approach for the controllable synthesis of ultrathin Pd nanowires along the one-dimensional (1D) direction. Ultrathin Pt films from one to several atomic layers were successfully decorated onto ultrathin Pd nanowires by utilizing Cu UPD deposition, and followed by in-situ redox replacement reaction of UPD Cu by Pt. The core–shell structure and composition of the Pd@Pt ultrathin nanowires have been verified using transmission electron microscopy and energy dispersive X-ray spectrometry. The core–shell Pd@Pt ultrathin nanowires exhibited comparative electrocatalytic activity and improved durability for the oxygen reduction reaction in comparison with commercial Pt black. The …

Effect Of Fe2+/Fe3+Interconvertion On Reduction Behavior Of Fe3+ In Acidic Electrolytes, Jian-Xin Qin, Feng Lin, Wen-Ping Liu, Chao Chen, Meng-De Ren

Journal of Electrochemistry

The influences of ferrous/ferric (Fe²⁺/Fe³⁺) interconvertion on electrochemical reduction and electrode reaction of Fe³⁺ were investigated by using linear sweep voltammetry, potentiostatic method and cyclic voltammetry (CV) in acidic electrolytes containing chloride ion (Cl^-) and sulfate ion (SO₄^2-). It was shown that the reduction process of Fe³⁺/Fe²⁺ would take place in two independent stages: (1) the reduction of Fe³⁺ to Fe²⁺ at E=0.35V and (2) the co-precipitation of Fe²⁺ by forming Fe(OH)₂ (E≤-0.3 V) instead of Fe. The major effect of Fe^{2+ …}

An Application Of M-Matrices To Preserve Bounded Positive Solutions To The Evolution Equations Of Biofilm Models, Richard S. Landry Jr.

LSU New Orleans Theses and Dissertations

In this work, we design a linear, two step implicit finite difference method to approximate the solutions of a biological system that describes the interaction between a microbial colony and a surrounding substrate. Three separate models are analyzed, all of which can be described as systems of partial differential equations (PDE)s with nonlinear diffusion and reaction, where the biological colony grows and decays based on the substrate bioavailability. The systems under investigation are all complex models describing the dynamics of biological films. In view of the difficulties to calculate analytical solutions of the models, we design here a numerical technique …