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Full-Text Articles in Physical Sciences and Mathematics

Study Of Nano Structure Mn/Alumina Catalyst Deactivation Through Catalytic Oxidation Of O-Vocs, Hosein Afshary May 2010

Study Of Nano Structure Mn/Alumina Catalyst Deactivation Through Catalytic Oxidation Of O-Vocs, Hosein Afshary

Hosein Afshary

the deactivation and selectivity behavior of nanostructure Mn/γ-Al2O3 catalyst in catalytic oxidation of an O-VOC (isopropanol) was studied. The polluted air was simulated and the catalyst was tested in the course of 50-h time-on-stream. Characterization of fresh and used catalysts was done using FT-IR, XRD, SEM and EDS methods. Comparing the testing results of this catalyst and that of the industrial Pt/Al2O3 catalyst showed that prepared catalyst can be suitable for substitution with the expensive pt/Al2O3 catalyst in environmental applications.


Investigation Of Deactivation Of Transition Metal Oxide Catalysts Supported On Γ-Al2o3 During Catalytic Oxidation Of Some Oxygen Containing Vocs In A Tubular Reactor, Hosein Afshary Feb 2010

Investigation Of Deactivation Of Transition Metal Oxide Catalysts Supported On Γ-Al2o3 During Catalytic Oxidation Of Some Oxygen Containing Vocs In A Tubular Reactor, Hosein Afshary

Hosein Afshary

It is necessary to decrease the emission of Volatile organic compound ( VOCs ) to air and among of all destructive techniques used for decreasing these compounds, Catalytic Oxidation is considered a suitable technique but deactivation of catalysts through catalytic processes is one of the major problems and most be studied. In this Project, at First, gamma alumina supported metal oxide catalysts were made and also industrial Pt catalyst was prepared. Then structure of these catalysts was studied using XRD, SEM and FT-IR techniques. These techniques approved the nanostructure of catalysts. The amount of supported metals in each catalyst was …


Design And Development Of Highly Active, Nanoengineered, Platinum Based Core-Shell Electrodes For Proton Exchange Membrane Fuel Cells, Seth Louis Knupp Jan 2010

Design And Development Of Highly Active, Nanoengineered, Platinum Based Core-Shell Electrodes For Proton Exchange Membrane Fuel Cells, Seth Louis Knupp

Legacy Theses & Dissertations (2009 - 2024)

Highly active nanoengineered core-shell electrocatalyst have a great potential to be used as fuel cell electrodes. They can alleviate problems related with commercial carbon supported platinum by simultaneously lowering cost while enhancing reaction kinetics and overall performance. More recently, use of nanoengineered core-shell electrode structures have showed their ability to enhance the stability and overall lifetime of the catalyst without sacrificing the electrode's performance. We studied the potential of using highly active core-shell nanoparticles supported on carbon nanomaterials as fuel cell electrodes.


An Efficient Synthesis Of Schiff Bases Containing Benzimidazole Moiety Catalyzed By Transition Metal Nitrates, Akbar Mobinikhaledi, Naser Foroughifar, Mehdi Kalhor Jan 2010

An Efficient Synthesis Of Schiff Bases Containing Benzimidazole Moiety Catalyzed By Transition Metal Nitrates, Akbar Mobinikhaledi, Naser Foroughifar, Mehdi Kalhor

Turkish Journal of Chemistry

A simple and efficient method has been developed for the synthesis of some novel Schiff bases via the reaction of aromatic aldehydes with 2-aminobenzimidazole by using catalytic amount of M(NO_3)_2.xH_2O in an organic solvent at room temperature. Some advantages of this protocol are its very good yields, use of available catalysts, simple workup procedure, and short reaction times.


Immobilization Of The Aminopeptidase From Aeromonas Proteolytica On Mg2+/Al3+ Layered Double Hydroxide Particles, Steven T. Frey, Stephanie L. Guilmet, Richard G. Egan Iii, Alyssa Bennett, Sarah R. Soltau, Richard C. Holz Jan 2010

Immobilization Of The Aminopeptidase From Aeromonas Proteolytica On Mg2+/Al3+ Layered Double Hydroxide Particles, Steven T. Frey, Stephanie L. Guilmet, Richard G. Egan Iii, Alyssa Bennett, Sarah R. Soltau, Richard C. Holz

Chemistry Faculty Research and Publications

A novel biomaterial formed by the immobilization of the Aminopeptidase from Aeromonas proteolytica (AAP) on synthetic Mg2+ and Al3+ ion-containing layered double hydroxide (LDH) particles was prepared. Immobilization of AAP on the LDH particles in a buffered, aqueous mixture is rapid such that the maximum loading capacity, 1 × 10−9 moles of AAP/mg LDH, is achieved in a few minutes. X-ray powder diffraction of LDH samples before and after treatment with AAP indicates that the enzyme does not intercalate between the layers of LDH, but instead binds to the surface. Treatment of AAP/LDH with various amounts of …