Georgia State University Perimeter College Decatur - Chemistry
Professor of Chemistry - Georgia State University - A Unit of University System of Georgia
Higher Education
Maher
Atteya, Ph.D.
Clarkston, Georgia
I had been teaching General Chemistry at Life University since 1998. I did write two lab manuals for our students at Life University and both manuals are copyrighted by the congress library. I also used Blackboard as an extra tool to communicate, to chat and to teach my students at my office hours.
In 1999 I was working and Georgia Perimeter College as adjunct faculty and since 2000, I have been teaching chemistry as a tenure track chemistry assistant professor at Georgia Perimeter College (GPC). I taught general and survey of chemistry courses. Typically I teach about 2-3 courses per semester online including summer and I teach on-campus 2 – 3 classes as well. I attended several educational workshops and conferences. Both teaching and workshop training helped me develop my teaching philosophy.
I was among other 2 more chemistry faculty who had started the online chemistry classes in the introductory and general chemistry in Georgia Perimeter College.
In the summer 2010 semester, I did pilot Respondus Lock Down Browser for all the quizzes and exams the students took.
Since 2008 I have been appointed as a fellow at Clark Atlanta University conducting research at the Center of Fiber and Nano scale Materials. Also, I was involved in supervising summer research for undergraduate students and interns. Furthermore, I worked very closely with couple Ph.D. candidates and helped them in publishing their work and also supervise their work in the lab.
I did use different methods of teaching – beside the traditional method of teaching - to keep my classes interactive and the students involved and interested. Some of these methods are:
Flipped Class model and hybrid. These methods are very valuable in improving the students learning and understanding for the topics taught and discussed.
In 2014, I did develop and teach 2 hybrid lab and later 2015 I did develop fully online lab and I am still teaching them. In 2016 my results were published in our University.
Nano Science-PLASM Researcher/Advisor
Maher worked at Clark Atlanta University as a Nano Science-PLASM Researcher/Advisor
Representative of 2 year community colleges at the Nano Science Research and Technology Board
Working with graduate and undergraduate students in their research topics during the summer semesters
Assistant Professor of Chemistry
Teaching Survey Chemistry 1 and 2 lectures and labs, Principal of Chemistry 1 and 2 lectures and labs online Using WebCT Vista. Developing General Chemistry lectures which are taught online (virtually).
Associate Professor of Chemistry
Teaching undergraduate students general and general chemistry and organic chemistry. Using and developing several teaching methods:
Problem Based Lectures
POGIL
Flipped Lectures
to name a few.
Professor of Chemistry
Maher worked at Georgia State University Perimeter College as a Professor of Chemistry
Science Department Chair
Managing a science department which is a multiple disciplinary science department. 25 faculty and 10 staff at Decatur campus.
Professor of Chemistry
Maher worked at Georgia State University Perimeter College as a Professor of Chemistry
Instructor of Chemistry
Managing and teaching general chemistry and organic chemistry classes for the Chiropractic undergraduate students.
Adjunct Chemistry Faculty
Supervising undergraduate general chemistry labs.
Online Chemistry Instructor
Teaching organic and general chemistry fully online for senior high school students as well as undergraduate students.
Ph.D. in Applied Chemistry - Minor: Petroleum Engineering
Applied Chemistry
M.S. in Chemistry
Inorganic Physical Chemistry
Post Doctoral Studies in surface/Heterogeneous. Catalysis related to the Environment
Physical Chemistry
Certification and Acknowledgment Award
Certification and Acknowledgment Award for post doctoral research at University of Denver.
Outstanding Achievement Award
Outstanding Achievement Award for post doctoral research at University of Denver.
Symposia Preprints, Div. Fuel. Chem., Am. Chem. Soc
Previously reported research, demonstrating a role of adsorbed molecular oxygen in the reaction of ozone with soot particles and in their hydration, has been extended to explore the interaction between O2 and SO2, O3, H2O, NH3, NO2 and NO at the soot surface as well as the effect of these adsorbates on each other. Electron paramagnetic resonance (EPR) and microgravimetry have revealed the extent of interactions between some competing reactants on soot. EPR has been used as a probe of the surface behavior of paramagnetic species (O2, NO2, NO) through their effect on the intensity of a large signal which is the result of the high concentration of unpaired electrons in soots. The effects of diamagnetic reactants (H2O, NH3, SO2) also are measured through their influence on the paramagnetic adsorbates and thus on the EPR signal. Microgravimetric measurements of adsorption and changes in the mass resulting from surface reactions also have enabled interpretations of the behavior of reactants on soot particles. Details of the modes of adsorption of SO2, NO2 and NH3 on n-hexane soot have emerged from these measurements as well.
Symposia Preprints, Div. Fuel. Chem., Am. Chem. Soc
Previously reported research, demonstrating a role of adsorbed molecular oxygen in the reaction of ozone with soot particles and in their hydration, has been extended to explore the interaction between O2 and SO2, O3, H2O, NH3, NO2 and NO at the soot surface as well as the effect of these adsorbates on each other. Electron paramagnetic resonance (EPR) and microgravimetry have revealed the extent of interactions between some competing reactants on soot. EPR has been used as a probe of the surface behavior of paramagnetic species (O2, NO2, NO) through their effect on the intensity of a large signal which is the result of the high concentration of unpaired electrons in soots. The effects of diamagnetic reactants (H2O, NH3, SO2) also are measured through their influence on the paramagnetic adsorbates and thus on the EPR signal. Microgravimetric measurements of adsorption and changes in the mass resulting from surface reactions also have enabled interpretations of the behavior of reactants on soot particles. Details of the modes of adsorption of SO2, NO2 and NH3 on n-hexane soot have emerged from these measurements as well.
Polymer Preprints, v.51, 2010, p. 650.
Fabrication of Functional Conductive Nanofibers Compose of A,_-bi-DNP-poly(2- methoxystyrene), Polystyrene Including Single Walled Carbon Nanotubes for Studying Materialcell Interactions and Gold Nanoparticles/synthetic Functional Polymer Nanofibers for B,"
Symposia Preprints, Div. Fuel. Chem., Am. Chem. Soc
Previously reported research, demonstrating a role of adsorbed molecular oxygen in the reaction of ozone with soot particles and in their hydration, has been extended to explore the interaction between O2 and SO2, O3, H2O, NH3, NO2 and NO at the soot surface as well as the effect of these adsorbates on each other. Electron paramagnetic resonance (EPR) and microgravimetry have revealed the extent of interactions between some competing reactants on soot. EPR has been used as a probe of the surface behavior of paramagnetic species (O2, NO2, NO) through their effect on the intensity of a large signal which is the result of the high concentration of unpaired electrons in soots. The effects of diamagnetic reactants (H2O, NH3, SO2) also are measured through their influence on the paramagnetic adsorbates and thus on the EPR signal. Microgravimetric measurements of adsorption and changes in the mass resulting from surface reactions also have enabled interpretations of the behavior of reactants on soot particles. Details of the modes of adsorption of SO2, NO2 and NH3 on n-hexane soot have emerged from these measurements as well.
Polymer Preprints, v.51, 2010, p. 650.
Fabrication of Functional Conductive Nanofibers Compose of A,_-bi-DNP-poly(2- methoxystyrene), Polystyrene Including Single Walled Carbon Nanotubes for Studying Materialcell Interactions and Gold Nanoparticles/synthetic Functional Polymer Nanofibers for B,"
Carbon
Previously reported research, demonstrating a role of adsorbed molecular oxygen in the reaction of ozone with soot particles and in their hydration, has been extended to explore the interaction between O2 and SO2, O3, H2O, NH3, NO2 and NO at the soot surface as well as the effect of these adsorbates on each other. Electron paramagnetic resonance (EPR) and microgravimetry have revealed the extent of interactions between some competing reactants on soot. EPR has been used as a probe of the surface behavior of paramagnetic species (O2, NO2, NO) through their effect on the intensity of a large signal which is the result of the high concentration of unpaired electrons in soots. The effects of diamagnetic reactants (H2O, NH3, SO2) also are measured through their influence on the paramagnetic adsorbates and thus on the EPR signal. Microgravimetric measurements of adsorption and changes in the mass resulting from surface reactions also have enabled interpretations of the behavior of reactants on soot particles. Details of the modes of adsorption of SO2, NO2 and NH3 on n-hexane soot have emerged from these measurements as well.
Symposia Preprints, Div. Fuel. Chem., Am. Chem. Soc
Previously reported research, demonstrating a role of adsorbed molecular oxygen in the reaction of ozone with soot particles and in their hydration, has been extended to explore the interaction between O2 and SO2, O3, H2O, NH3, NO2 and NO at the soot surface as well as the effect of these adsorbates on each other. Electron paramagnetic resonance (EPR) and microgravimetry have revealed the extent of interactions between some competing reactants on soot. EPR has been used as a probe of the surface behavior of paramagnetic species (O2, NO2, NO) through their effect on the intensity of a large signal which is the result of the high concentration of unpaired electrons in soots. The effects of diamagnetic reactants (H2O, NH3, SO2) also are measured through their influence on the paramagnetic adsorbates and thus on the EPR signal. Microgravimetric measurements of adsorption and changes in the mass resulting from surface reactions also have enabled interpretations of the behavior of reactants on soot particles. Details of the modes of adsorption of SO2, NO2 and NH3 on n-hexane soot have emerged from these measurements as well.
Polymer Preprints, v.51, 2010, p. 650.
Fabrication of Functional Conductive Nanofibers Compose of A,_-bi-DNP-poly(2- methoxystyrene), Polystyrene Including Single Walled Carbon Nanotubes for Studying Materialcell Interactions and Gold Nanoparticles/synthetic Functional Polymer Nanofibers for B,"
Carbon
Previously reported research, demonstrating a role of adsorbed molecular oxygen in the reaction of ozone with soot particles and in their hydration, has been extended to explore the interaction between O2 and SO2, O3, H2O, NH3, NO2 and NO at the soot surface as well as the effect of these adsorbates on each other. Electron paramagnetic resonance (EPR) and microgravimetry have revealed the extent of interactions between some competing reactants on soot. EPR has been used as a probe of the surface behavior of paramagnetic species (O2, NO2, NO) through their effect on the intensity of a large signal which is the result of the high concentration of unpaired electrons in soots. The effects of diamagnetic reactants (H2O, NH3, SO2) also are measured through their influence on the paramagnetic adsorbates and thus on the EPR signal. Microgravimetric measurements of adsorption and changes in the mass resulting from surface reactions also have enabled interpretations of the behavior of reactants on soot particles. Details of the modes of adsorption of SO2, NO2 and NH3 on n-hexane soot have emerged from these measurements as well.
Chem. of Materials
Using an in-situ pulsed reactor GC-MS system, the thermal decomposition of organophosphorus compounds (as models of nerve agents) has been compared with their destructive adsorption on high surface area magnesium oxide. Dramatically lower temperatures are required when MgO is present. Volatile products evolved were formic acid, water, alcohols, and alkenes. At higher temperatures CO, CH4, and water predominated. Phosphorus residues remained completely immobilized. Addition of water enhanced the facility of MgO to destroy these compounds, and in fact, water pulses were found to partially regenerate a spent MgO bed. Using 110 labeling, some aspects of the reaction mechanisms were clarified and in particular showed that oxygen scrambling occurred. Surface OH and MgO groups transferred oxygen in the formation of formic acid, and surface mobility and reactivity of adsorbed groups was very high. The substantial capacity of high surface area MgO for destruction and immobilization of such toxic substances makes it attractive for air purification schemes as well as solid reagents for destruction and immobilization of bulk quantities of hazardous phosphorus compounds or organohalides. Fourier Transform Infrared Photoacoustic Spectroscopy Study
Symposia Preprints, Div. Fuel. Chem., Am. Chem. Soc
Previously reported research, demonstrating a role of adsorbed molecular oxygen in the reaction of ozone with soot particles and in their hydration, has been extended to explore the interaction between O2 and SO2, O3, H2O, NH3, NO2 and NO at the soot surface as well as the effect of these adsorbates on each other. Electron paramagnetic resonance (EPR) and microgravimetry have revealed the extent of interactions between some competing reactants on soot. EPR has been used as a probe of the surface behavior of paramagnetic species (O2, NO2, NO) through their effect on the intensity of a large signal which is the result of the high concentration of unpaired electrons in soots. The effects of diamagnetic reactants (H2O, NH3, SO2) also are measured through their influence on the paramagnetic adsorbates and thus on the EPR signal. Microgravimetric measurements of adsorption and changes in the mass resulting from surface reactions also have enabled interpretations of the behavior of reactants on soot particles. Details of the modes of adsorption of SO2, NO2 and NH3 on n-hexane soot have emerged from these measurements as well.
Polymer Preprints, v.51, 2010, p. 650.
Fabrication of Functional Conductive Nanofibers Compose of A,_-bi-DNP-poly(2- methoxystyrene), Polystyrene Including Single Walled Carbon Nanotubes for Studying Materialcell Interactions and Gold Nanoparticles/synthetic Functional Polymer Nanofibers for B,"
Carbon
Previously reported research, demonstrating a role of adsorbed molecular oxygen in the reaction of ozone with soot particles and in their hydration, has been extended to explore the interaction between O2 and SO2, O3, H2O, NH3, NO2 and NO at the soot surface as well as the effect of these adsorbates on each other. Electron paramagnetic resonance (EPR) and microgravimetry have revealed the extent of interactions between some competing reactants on soot. EPR has been used as a probe of the surface behavior of paramagnetic species (O2, NO2, NO) through their effect on the intensity of a large signal which is the result of the high concentration of unpaired electrons in soots. The effects of diamagnetic reactants (H2O, NH3, SO2) also are measured through their influence on the paramagnetic adsorbates and thus on the EPR signal. Microgravimetric measurements of adsorption and changes in the mass resulting from surface reactions also have enabled interpretations of the behavior of reactants on soot particles. Details of the modes of adsorption of SO2, NO2 and NH3 on n-hexane soot have emerged from these measurements as well.
Chem. of Materials
Using an in-situ pulsed reactor GC-MS system, the thermal decomposition of organophosphorus compounds (as models of nerve agents) has been compared with their destructive adsorption on high surface area magnesium oxide. Dramatically lower temperatures are required when MgO is present. Volatile products evolved were formic acid, water, alcohols, and alkenes. At higher temperatures CO, CH4, and water predominated. Phosphorus residues remained completely immobilized. Addition of water enhanced the facility of MgO to destroy these compounds, and in fact, water pulses were found to partially regenerate a spent MgO bed. Using 110 labeling, some aspects of the reaction mechanisms were clarified and in particular showed that oxygen scrambling occurred. Surface OH and MgO groups transferred oxygen in the formation of formic acid, and surface mobility and reactivity of adsorbed groups was very high. The substantial capacity of high surface area MgO for destruction and immobilization of such toxic substances makes it attractive for air purification schemes as well as solid reagents for destruction and immobilization of bulk quantities of hazardous phosphorus compounds or organohalides. Fourier Transform Infrared Photoacoustic Spectroscopy Study
Chem. Materials
Heats of adsorption (immersion) were measured via a solution calorimeter for a series of heteroatom (oxygen, sulfur, phosphorus) containing organic compounds on thermally activated magnesium oxide (heat treated at 7000C overnight in vacuo followed by cooling to room temperature). For phosphates, phosphites, and phosphines the heats of adsorption were high and showed a small dependence on substituent effects. For sulfur compounds, -S-H-containing compounds yielded the highest values. For oxygen systems very high heats of adsorption were found for carbonyl compounds. In addition, the strongly basic nature of the MgO surface was demonstrated by the extremely high heats of adsorption/reaction with carboxylic acids. Heats observed for 1-butanol adsorption varied linearly with MgO surface area. Surprisingly, cyclohexane dilution of 1-butanol caused a dramatic lowering of adsorption heats, demonstrating the competitive nature of even such unreactive solvents. The observed heats of adsorption/reaction combined with spectroscopic data allowed some conclusions about the type of surface bonding that took place. The strong interactions of several of these organics demonstrate the nature of heat-treated MgO as a destructive adsorbent for many toxic chemicals. Since MgO is nontoxic and inexpensive and can be prepared in highly surface activated forms, it shows promise for use in air-purification schemes.
Symposia Preprints, Div. Fuel. Chem., Am. Chem. Soc
Previously reported research, demonstrating a role of adsorbed molecular oxygen in the reaction of ozone with soot particles and in their hydration, has been extended to explore the interaction between O2 and SO2, O3, H2O, NH3, NO2 and NO at the soot surface as well as the effect of these adsorbates on each other. Electron paramagnetic resonance (EPR) and microgravimetry have revealed the extent of interactions between some competing reactants on soot. EPR has been used as a probe of the surface behavior of paramagnetic species (O2, NO2, NO) through their effect on the intensity of a large signal which is the result of the high concentration of unpaired electrons in soots. The effects of diamagnetic reactants (H2O, NH3, SO2) also are measured through their influence on the paramagnetic adsorbates and thus on the EPR signal. Microgravimetric measurements of adsorption and changes in the mass resulting from surface reactions also have enabled interpretations of the behavior of reactants on soot particles. Details of the modes of adsorption of SO2, NO2 and NH3 on n-hexane soot have emerged from these measurements as well.
Polymer Preprints, v.51, 2010, p. 650.
Fabrication of Functional Conductive Nanofibers Compose of A,_-bi-DNP-poly(2- methoxystyrene), Polystyrene Including Single Walled Carbon Nanotubes for Studying Materialcell Interactions and Gold Nanoparticles/synthetic Functional Polymer Nanofibers for B,"
Carbon
Previously reported research, demonstrating a role of adsorbed molecular oxygen in the reaction of ozone with soot particles and in their hydration, has been extended to explore the interaction between O2 and SO2, O3, H2O, NH3, NO2 and NO at the soot surface as well as the effect of these adsorbates on each other. Electron paramagnetic resonance (EPR) and microgravimetry have revealed the extent of interactions between some competing reactants on soot. EPR has been used as a probe of the surface behavior of paramagnetic species (O2, NO2, NO) through their effect on the intensity of a large signal which is the result of the high concentration of unpaired electrons in soots. The effects of diamagnetic reactants (H2O, NH3, SO2) also are measured through their influence on the paramagnetic adsorbates and thus on the EPR signal. Microgravimetric measurements of adsorption and changes in the mass resulting from surface reactions also have enabled interpretations of the behavior of reactants on soot particles. Details of the modes of adsorption of SO2, NO2 and NH3 on n-hexane soot have emerged from these measurements as well.
Chem. of Materials
Using an in-situ pulsed reactor GC-MS system, the thermal decomposition of organophosphorus compounds (as models of nerve agents) has been compared with their destructive adsorption on high surface area magnesium oxide. Dramatically lower temperatures are required when MgO is present. Volatile products evolved were formic acid, water, alcohols, and alkenes. At higher temperatures CO, CH4, and water predominated. Phosphorus residues remained completely immobilized. Addition of water enhanced the facility of MgO to destroy these compounds, and in fact, water pulses were found to partially regenerate a spent MgO bed. Using 110 labeling, some aspects of the reaction mechanisms were clarified and in particular showed that oxygen scrambling occurred. Surface OH and MgO groups transferred oxygen in the formation of formic acid, and surface mobility and reactivity of adsorbed groups was very high. The substantial capacity of high surface area MgO for destruction and immobilization of such toxic substances makes it attractive for air purification schemes as well as solid reagents for destruction and immobilization of bulk quantities of hazardous phosphorus compounds or organohalides. Fourier Transform Infrared Photoacoustic Spectroscopy Study
Chem. Materials
Heats of adsorption (immersion) were measured via a solution calorimeter for a series of heteroatom (oxygen, sulfur, phosphorus) containing organic compounds on thermally activated magnesium oxide (heat treated at 7000C overnight in vacuo followed by cooling to room temperature). For phosphates, phosphites, and phosphines the heats of adsorption were high and showed a small dependence on substituent effects. For sulfur compounds, -S-H-containing compounds yielded the highest values. For oxygen systems very high heats of adsorption were found for carbonyl compounds. In addition, the strongly basic nature of the MgO surface was demonstrated by the extremely high heats of adsorption/reaction with carboxylic acids. Heats observed for 1-butanol adsorption varied linearly with MgO surface area. Surprisingly, cyclohexane dilution of 1-butanol caused a dramatic lowering of adsorption heats, demonstrating the competitive nature of even such unreactive solvents. The observed heats of adsorption/reaction combined with spectroscopic data allowed some conclusions about the type of surface bonding that took place. The strong interactions of several of these organics demonstrate the nature of heat-treated MgO as a destructive adsorbent for many toxic chemicals. Since MgO is nontoxic and inexpensive and can be prepared in highly surface activated forms, it shows promise for use in air-purification schemes.
Journal: Atmospheric Environment
Microgravimetric measurements of the hydration of several different black carbons or soots and a series of commercial carbon blacks have been carried out, over a relative humidity range of 20–85%, in an extension of earlier work with the model n-hexane soot. All adsorption isotherms are of type III and were analyzed by the use of the Dubinin–Radushkevich (DR) equation which, although applicable over a limited range of intermediate relative humidity values, allows identification of chemisorption limit and onset of multilayer formation. While surface area determines the maximum adsorption possible for a given type, surface functionalities are determinative at lower humidity and are characteristic of the soot-producing fuel. Aging of carbon particles and oxygen chemisorption as well as O2 physisorption strongly influence the extent of hydration for those soots studied, such as JP-8 aviation and diesel fuels. Infrared spectra confirm the surface oxidation of JP-8 soot by its reaction with O3, a reaction of probable atmospheric importance, as underlying its increased hydration.less
Symposia Preprints, Div. Fuel. Chem., Am. Chem. Soc
Previously reported research, demonstrating a role of adsorbed molecular oxygen in the reaction of ozone with soot particles and in their hydration, has been extended to explore the interaction between O2 and SO2, O3, H2O, NH3, NO2 and NO at the soot surface as well as the effect of these adsorbates on each other. Electron paramagnetic resonance (EPR) and microgravimetry have revealed the extent of interactions between some competing reactants on soot. EPR has been used as a probe of the surface behavior of paramagnetic species (O2, NO2, NO) through their effect on the intensity of a large signal which is the result of the high concentration of unpaired electrons in soots. The effects of diamagnetic reactants (H2O, NH3, SO2) also are measured through their influence on the paramagnetic adsorbates and thus on the EPR signal. Microgravimetric measurements of adsorption and changes in the mass resulting from surface reactions also have enabled interpretations of the behavior of reactants on soot particles. Details of the modes of adsorption of SO2, NO2 and NH3 on n-hexane soot have emerged from these measurements as well.
Polymer Preprints, v.51, 2010, p. 650.
Fabrication of Functional Conductive Nanofibers Compose of A,_-bi-DNP-poly(2- methoxystyrene), Polystyrene Including Single Walled Carbon Nanotubes for Studying Materialcell Interactions and Gold Nanoparticles/synthetic Functional Polymer Nanofibers for B,"
Carbon
Previously reported research, demonstrating a role of adsorbed molecular oxygen in the reaction of ozone with soot particles and in their hydration, has been extended to explore the interaction between O2 and SO2, O3, H2O, NH3, NO2 and NO at the soot surface as well as the effect of these adsorbates on each other. Electron paramagnetic resonance (EPR) and microgravimetry have revealed the extent of interactions between some competing reactants on soot. EPR has been used as a probe of the surface behavior of paramagnetic species (O2, NO2, NO) through their effect on the intensity of a large signal which is the result of the high concentration of unpaired electrons in soots. The effects of diamagnetic reactants (H2O, NH3, SO2) also are measured through their influence on the paramagnetic adsorbates and thus on the EPR signal. Microgravimetric measurements of adsorption and changes in the mass resulting from surface reactions also have enabled interpretations of the behavior of reactants on soot particles. Details of the modes of adsorption of SO2, NO2 and NH3 on n-hexane soot have emerged from these measurements as well.
Chem. of Materials
Using an in-situ pulsed reactor GC-MS system, the thermal decomposition of organophosphorus compounds (as models of nerve agents) has been compared with their destructive adsorption on high surface area magnesium oxide. Dramatically lower temperatures are required when MgO is present. Volatile products evolved were formic acid, water, alcohols, and alkenes. At higher temperatures CO, CH4, and water predominated. Phosphorus residues remained completely immobilized. Addition of water enhanced the facility of MgO to destroy these compounds, and in fact, water pulses were found to partially regenerate a spent MgO bed. Using 110 labeling, some aspects of the reaction mechanisms were clarified and in particular showed that oxygen scrambling occurred. Surface OH and MgO groups transferred oxygen in the formation of formic acid, and surface mobility and reactivity of adsorbed groups was very high. The substantial capacity of high surface area MgO for destruction and immobilization of such toxic substances makes it attractive for air purification schemes as well as solid reagents for destruction and immobilization of bulk quantities of hazardous phosphorus compounds or organohalides. Fourier Transform Infrared Photoacoustic Spectroscopy Study
Chem. Materials
Heats of adsorption (immersion) were measured via a solution calorimeter for a series of heteroatom (oxygen, sulfur, phosphorus) containing organic compounds on thermally activated magnesium oxide (heat treated at 7000C overnight in vacuo followed by cooling to room temperature). For phosphates, phosphites, and phosphines the heats of adsorption were high and showed a small dependence on substituent effects. For sulfur compounds, -S-H-containing compounds yielded the highest values. For oxygen systems very high heats of adsorption were found for carbonyl compounds. In addition, the strongly basic nature of the MgO surface was demonstrated by the extremely high heats of adsorption/reaction with carboxylic acids. Heats observed for 1-butanol adsorption varied linearly with MgO surface area. Surprisingly, cyclohexane dilution of 1-butanol caused a dramatic lowering of adsorption heats, demonstrating the competitive nature of even such unreactive solvents. The observed heats of adsorption/reaction combined with spectroscopic data allowed some conclusions about the type of surface bonding that took place. The strong interactions of several of these organics demonstrate the nature of heat-treated MgO as a destructive adsorbent for many toxic chemicals. Since MgO is nontoxic and inexpensive and can be prepared in highly surface activated forms, it shows promise for use in air-purification schemes.
Journal: Atmospheric Environment
Microgravimetric measurements of the hydration of several different black carbons or soots and a series of commercial carbon blacks have been carried out, over a relative humidity range of 20–85%, in an extension of earlier work with the model n-hexane soot. All adsorption isotherms are of type III and were analyzed by the use of the Dubinin–Radushkevich (DR) equation which, although applicable over a limited range of intermediate relative humidity values, allows identification of chemisorption limit and onset of multilayer formation. While surface area determines the maximum adsorption possible for a given type, surface functionalities are determinative at lower humidity and are characteristic of the soot-producing fuel. Aging of carbon particles and oxygen chemisorption as well as O2 physisorption strongly influence the extent of hydration for those soots studied, such as JP-8 aviation and diesel fuels. Infrared spectra confirm the surface oxidation of JP-8 soot by its reaction with O3, a reaction of probable atmospheric importance, as underlying its increased hydration.less
Journal: Atmospheric Environment
Microgravimetric measurements of the hydration of several different black carbons or soots and a series of commercial carbon blacks have been carried out, over a relative humidity range of 20–85%, in an extension of earlier work with the model n-hexane soot. All adsorption isotherms are of type III and were analyzed by the use of the Dubinin–Radushkevich (DR) equation which, although applicable over a limited range of intermediate relative humidity values, allows identification of chemisorption limit and onset of multilayer formation. While surface area determines the maximum adsorption possible for a given type, surface functionalities are determinative at lower humidity and are characteristic of the soot-producing fuel. Aging of carbon particles and oxygen chemisorption as well as O2 physisorption strongly influence the extent of hydration for those soots studied, such as JP-8 aviation and diesel fuels. Infrared spectra confirm the surface oxidation of JP-8 soot by its reaction with O3, a reaction of probable atmospheric importance, as underlying its increased hydration.
Symposia Preprints, Div. Fuel. Chem., Am. Chem. Soc
Previously reported research, demonstrating a role of adsorbed molecular oxygen in the reaction of ozone with soot particles and in their hydration, has been extended to explore the interaction between O2 and SO2, O3, H2O, NH3, NO2 and NO at the soot surface as well as the effect of these adsorbates on each other. Electron paramagnetic resonance (EPR) and microgravimetry have revealed the extent of interactions between some competing reactants on soot. EPR has been used as a probe of the surface behavior of paramagnetic species (O2, NO2, NO) through their effect on the intensity of a large signal which is the result of the high concentration of unpaired electrons in soots. The effects of diamagnetic reactants (H2O, NH3, SO2) also are measured through their influence on the paramagnetic adsorbates and thus on the EPR signal. Microgravimetric measurements of adsorption and changes in the mass resulting from surface reactions also have enabled interpretations of the behavior of reactants on soot particles. Details of the modes of adsorption of SO2, NO2 and NH3 on n-hexane soot have emerged from these measurements as well.
Polymer Preprints, v.51, 2010, p. 650.
Fabrication of Functional Conductive Nanofibers Compose of A,_-bi-DNP-poly(2- methoxystyrene), Polystyrene Including Single Walled Carbon Nanotubes for Studying Materialcell Interactions and Gold Nanoparticles/synthetic Functional Polymer Nanofibers for B,"
Carbon
Previously reported research, demonstrating a role of adsorbed molecular oxygen in the reaction of ozone with soot particles and in their hydration, has been extended to explore the interaction between O2 and SO2, O3, H2O, NH3, NO2 and NO at the soot surface as well as the effect of these adsorbates on each other. Electron paramagnetic resonance (EPR) and microgravimetry have revealed the extent of interactions between some competing reactants on soot. EPR has been used as a probe of the surface behavior of paramagnetic species (O2, NO2, NO) through their effect on the intensity of a large signal which is the result of the high concentration of unpaired electrons in soots. The effects of diamagnetic reactants (H2O, NH3, SO2) also are measured through their influence on the paramagnetic adsorbates and thus on the EPR signal. Microgravimetric measurements of adsorption and changes in the mass resulting from surface reactions also have enabled interpretations of the behavior of reactants on soot particles. Details of the modes of adsorption of SO2, NO2 and NH3 on n-hexane soot have emerged from these measurements as well.
Chem. of Materials
Using an in-situ pulsed reactor GC-MS system, the thermal decomposition of organophosphorus compounds (as models of nerve agents) has been compared with their destructive adsorption on high surface area magnesium oxide. Dramatically lower temperatures are required when MgO is present. Volatile products evolved were formic acid, water, alcohols, and alkenes. At higher temperatures CO, CH4, and water predominated. Phosphorus residues remained completely immobilized. Addition of water enhanced the facility of MgO to destroy these compounds, and in fact, water pulses were found to partially regenerate a spent MgO bed. Using 110 labeling, some aspects of the reaction mechanisms were clarified and in particular showed that oxygen scrambling occurred. Surface OH and MgO groups transferred oxygen in the formation of formic acid, and surface mobility and reactivity of adsorbed groups was very high. The substantial capacity of high surface area MgO for destruction and immobilization of such toxic substances makes it attractive for air purification schemes as well as solid reagents for destruction and immobilization of bulk quantities of hazardous phosphorus compounds or organohalides. Fourier Transform Infrared Photoacoustic Spectroscopy Study
Chem. Materials
Heats of adsorption (immersion) were measured via a solution calorimeter for a series of heteroatom (oxygen, sulfur, phosphorus) containing organic compounds on thermally activated magnesium oxide (heat treated at 7000C overnight in vacuo followed by cooling to room temperature). For phosphates, phosphites, and phosphines the heats of adsorption were high and showed a small dependence on substituent effects. For sulfur compounds, -S-H-containing compounds yielded the highest values. For oxygen systems very high heats of adsorption were found for carbonyl compounds. In addition, the strongly basic nature of the MgO surface was demonstrated by the extremely high heats of adsorption/reaction with carboxylic acids. Heats observed for 1-butanol adsorption varied linearly with MgO surface area. Surprisingly, cyclohexane dilution of 1-butanol caused a dramatic lowering of adsorption heats, demonstrating the competitive nature of even such unreactive solvents. The observed heats of adsorption/reaction combined with spectroscopic data allowed some conclusions about the type of surface bonding that took place. The strong interactions of several of these organics demonstrate the nature of heat-treated MgO as a destructive adsorbent for many toxic chemicals. Since MgO is nontoxic and inexpensive and can be prepared in highly surface activated forms, it shows promise for use in air-purification schemes.
Journal: Atmospheric Environment
Microgravimetric measurements of the hydration of several different black carbons or soots and a series of commercial carbon blacks have been carried out, over a relative humidity range of 20–85%, in an extension of earlier work with the model n-hexane soot. All adsorption isotherms are of type III and were analyzed by the use of the Dubinin–Radushkevich (DR) equation which, although applicable over a limited range of intermediate relative humidity values, allows identification of chemisorption limit and onset of multilayer formation. While surface area determines the maximum adsorption possible for a given type, surface functionalities are determinative at lower humidity and are characteristic of the soot-producing fuel. Aging of carbon particles and oxygen chemisorption as well as O2 physisorption strongly influence the extent of hydration for those soots studied, such as JP-8 aviation and diesel fuels. Infrared spectra confirm the surface oxidation of JP-8 soot by its reaction with O3, a reaction of probable atmospheric importance, as underlying its increased hydration.less
Journal: Atmospheric Environment
Microgravimetric measurements of the hydration of several different black carbons or soots and a series of commercial carbon blacks have been carried out, over a relative humidity range of 20–85%, in an extension of earlier work with the model n-hexane soot. All adsorption isotherms are of type III and were analyzed by the use of the Dubinin–Radushkevich (DR) equation which, although applicable over a limited range of intermediate relative humidity values, allows identification of chemisorption limit and onset of multilayer formation. While surface area determines the maximum adsorption possible for a given type, surface functionalities are determinative at lower humidity and are characteristic of the soot-producing fuel. Aging of carbon particles and oxygen chemisorption as well as O2 physisorption strongly influence the extent of hydration for those soots studied, such as JP-8 aviation and diesel fuels. Infrared spectra confirm the surface oxidation of JP-8 soot by its reaction with O3, a reaction of probable atmospheric importance, as underlying its increased hydration.
Symposia Preprints, Div. Fuel. Chem,. Am. Chem. Soc.,
"Current research is related to the interaction of gas phase molecules with solid surfaces, and now is mostly focused on the nature and reactivity of black carbon (soot), produced through the combustion of fossil fuels. Previous work provided a characterization of the soot structure and surface which has been useful in studying its reactions, including their kinetics and mechanisms, with gaseous species of atmospheric interest. Recent research has emphasized the heterogeneous reactions of soot with oxides of nitrogen and sulfur, and ozone, studied through spectroscopic and microgravimetric techniques. Other questions being addressed by kinetics studies include catalysis, hydration mechanisms, the behavior of multiple reactants, and photochemical effects. Also under study is the role of the solid (soot) phase in these reactions, including unpaired electrons (by EPR), trace metals/mineral content, and particle size and morphology"
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2 year community colleges association, sub unit and affiliate of American Chemical Society organization. Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
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Presenting Summer Undergraduate Research Results/urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,570879530)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,570879530)
Editor/Member
Editing Chemistry Related Topics and Papers and Articles.urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Advisor /Member
Working with graduate and undergraduate students in their research topics during the summer semestersurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Georgia Science Teachers Association.urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
2 year community colleges association, sub unit and affiliate of American Chemical Society organization. Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Presenting Summer Undergraduate Research Results/urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,570879530)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,570879530)
Editor/Member
Editing Chemistry Related Topics and Papers and Articles.urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Advisor /Member
Working with graduate and undergraduate students in their research topics during the summer semestersurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Georgia Science Teachers Association.urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
2 year community colleges association, sub unit and affiliate of American Chemical Society organization. Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Presenting Summer Undergraduate Research Results/urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,570879530)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,570879530)
Editor/Member
Editing Chemistry Related Topics and Papers and Articles.urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Advisor /Member
Working with graduate and undergraduate students in their research topics during the summer semestersurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Georgia Science Teachers Association.urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
2 year community colleges association, sub unit and affiliate of American Chemical Society organization. Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Presenting Summer Undergraduate Research Results/urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,570879530)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,570879530)
Editor/Member
Editing Chemistry Related Topics and Papers and Articles.urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Advisor /Member
Working with graduate and undergraduate students in their research topics during the summer semestersurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Georgia Science Teachers Association.urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
2 year community colleges association, sub unit and affiliate of American Chemical Society organization. Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Presenting Summer Undergraduate Research Results/urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,570879530)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,570879530)
Editor/Member
Editing Chemistry Related Topics and Papers and Articles.urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Advisor /Member
Working with graduate and undergraduate students in their research topics during the summer semestersurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Georgia Science Teachers Association.urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
2 year community colleges association, sub unit and affiliate of American Chemical Society organization. Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571293577)
Member
Presenting Summer Undergraduate Research Results/urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,570879530)
Member
Attending and participating in workshops, seminars and webinarurn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,570879530)
Editor/Member
Editing Chemistry Related Topics and Papers and Articles.urn:li:fs_position:(ACoAABWibRoBtMA6HnihOur4I0g6gQsVlLdXgEQ,571294478)
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