Molecularly imprinted polymeric materials for adsorptive removal of nitrogen compounds from fuel oils
- Abdul-Quadir, Muhammad Sabiu
- Authors: Abdul-Quadir, Muhammad Sabiu
- Date: 2018
- Subjects: Polymerization , Organonitrogen compounds Nitrogen compounds
- Language: English
- Type: Thesis , Doctoral , DPhil
- Identifier: http://hdl.handle.net/10948/23426 , vital:30542
- Description: The deleterious effects of refractory polyaromatic hydrocarbons found in fuels such as organonitrogen compounds (quinoline, carbazole and its alkylated derivatives) are such that they emit NOx to the environment when combusted, thereby reducing air quality. These compounds also deactivate the catalyst used during fuel refinement and in catalytic converters of cars. Hydro-denitrogenation (HDN), a process currently being employed in petroleum refineries to eliminate organonitrogen compounds in fuels, is limited in treating these refractory compounds. Hence, this thesis describes the use of two separate complimentary approaches for the removal of organonitrogen compounds in fuel such as oxidative denitrogenation and adsorptive denitrogenation. The catalyzed oxidation of fuel oil model nitrogen containing compound, quinoline to quinoline N-oxide, was conducted under batch and continuous flow microreactor at 70°C by using tert-butylhydroperoxide (t-BuOOH) as oxidant and silica supported V2O5 as catalyst, followed by the selective adsorption of the quinoline N-oxide. An overall conversion of 62% quinoline N-oxide was observed. Quinoline-N-oxide in model fuel was absorbed by employing synthesized molecularly imprinted 2,6-pyridine-polybenzimidazole (2,6-PyPBI) nanofibers, 86% of quinoline-N-oxide was removed to give an adsorption capacity (qe) of 4.8 mg/g. DFT calculations to study the interactions of quinoline-N-oxide vs 2,6-PyPBI indicated that: (i) hydrogen bonding (through amino group of 2,6-PyPBI and oxygen atoms of the quinoline-N-oxide), (ii) pi-pi stacking and (iii) extensive number of van der Waals interactions took place. Several oxygenates from N-compounds were produced, thus, complicating the fuel matrix. Therefore, there is a need to move towards adsorptive denitrogenation. Poly-2-(1H-imidazol-2-yl)-4-phenol (PIMH) imprinted microspheres was prepared by suspension polymerization using 2-(2’-hydroxy-4-ethenylphenyl) imidazole as a functional monomer and ethylene glycol dimethacrylate as a crosslinker in the presence of various organonitrogen compounds (templates) to produce 2-(2’-hydroxy-4-ethenylphenyl) imidazole (PIMH). Imprinted microspheres show selectivity for various target model nitrogen-containing compounds with adsorption capacities of 6.8 ± 0.2 mg/g, 6.3 ± 0.3 mg/g and 5.8 ± 0.3 mg/g for quinoline, pyrimidine and carbazole, respectively. Adsorption selectivity increased in the order of quinoline (αi-r = 136.9) ˃ pyrimidine (αi-r = 126.2) ˃carbazole (αi-r = 86.3), when naphthalene was selected as a reference compound. Though, imprinted microspheres displayed excellent nitrogen compound removal both in model and real fuel, there was a need to improve the adsorbent adsorption capacity for N-compounds in fuel through the fabrication of imprinted nanofibers. Molecularly imprinted poly-2-(1H-imidazol-2-yl)-4-phenol nanofibers was prepared by electrospinning of 2-(2’-hydroxy-4-ethenylphenyl) imidazole (PIMH) in the presence of various organonitrogen compounds. These imprinted nanofibers show selectivity for various target model nitrogen-containing compounds with adsorption capacities of 11.7 ± 0.9 mg/g, 11.9 ± 0.8 mg/g and 11.3 ± 1.1 mg/g for quinoline, pyrimidine and carbazole, respectively. Adsorption selectivity increased in the order of pyrimidine (αi-r = 258.8) ˃ quinoline (αi-r = 235.5) ˃ carbazole (αi-r = 168.2). It further displayed excellent nitrogen removal in real fuel. The use of polybenzimidazole (PBI) nanofibers showed selective adsorption of organonitrogen compounds as imprinted sorbent also displayed high selectivity for their target model nitrogen-containing compounds with adsorption capacities of 11.4 ± 0.4 mg/g, 11.9 ± 0.2 mg/g and 10.9 ± 0.7 mg/g for quinoline, pyrimidine and carbazole respectively. Adsorption selectivity increased in the order of pyrimidine (αi-r = 241.5) ˃ quinoline (αi-r = 237.6) ˃ carbazole (αi-r = 170). Thermodynamic parameters obtained from isothermal titration calorimetry (ITC) revealed that quinoline-PIMH/PBI and pyrimidine-PIMH/PBI interactions are exothermic in nature, while carbazole-PIMH/PBI is endothermic in nature. DFT calculations indicated that π-π interactions/stacking and hydrogen bond interactions took place between N-compounds (carbazole, quinoline and pyrimidine) and adsorbent (PIMH and PBI). A significant reduction in the quantity of nitrogen containing compounds in hydrotreated fuel was observed (peak area reduction) when adsorbents (PIMH and PBI) was employed, however, the complex nature of organonitrogen compounds in fuel complicate the structure/function approach on MIPs for targeting these unwanted compounds.
- Full Text:
- Date Issued: 2018
- Authors: Abdul-Quadir, Muhammad Sabiu
- Date: 2018
- Subjects: Polymerization , Organonitrogen compounds Nitrogen compounds
- Language: English
- Type: Thesis , Doctoral , DPhil
- Identifier: http://hdl.handle.net/10948/23426 , vital:30542
- Description: The deleterious effects of refractory polyaromatic hydrocarbons found in fuels such as organonitrogen compounds (quinoline, carbazole and its alkylated derivatives) are such that they emit NOx to the environment when combusted, thereby reducing air quality. These compounds also deactivate the catalyst used during fuel refinement and in catalytic converters of cars. Hydro-denitrogenation (HDN), a process currently being employed in petroleum refineries to eliminate organonitrogen compounds in fuels, is limited in treating these refractory compounds. Hence, this thesis describes the use of two separate complimentary approaches for the removal of organonitrogen compounds in fuel such as oxidative denitrogenation and adsorptive denitrogenation. The catalyzed oxidation of fuel oil model nitrogen containing compound, quinoline to quinoline N-oxide, was conducted under batch and continuous flow microreactor at 70°C by using tert-butylhydroperoxide (t-BuOOH) as oxidant and silica supported V2O5 as catalyst, followed by the selective adsorption of the quinoline N-oxide. An overall conversion of 62% quinoline N-oxide was observed. Quinoline-N-oxide in model fuel was absorbed by employing synthesized molecularly imprinted 2,6-pyridine-polybenzimidazole (2,6-PyPBI) nanofibers, 86% of quinoline-N-oxide was removed to give an adsorption capacity (qe) of 4.8 mg/g. DFT calculations to study the interactions of quinoline-N-oxide vs 2,6-PyPBI indicated that: (i) hydrogen bonding (through amino group of 2,6-PyPBI and oxygen atoms of the quinoline-N-oxide), (ii) pi-pi stacking and (iii) extensive number of van der Waals interactions took place. Several oxygenates from N-compounds were produced, thus, complicating the fuel matrix. Therefore, there is a need to move towards adsorptive denitrogenation. Poly-2-(1H-imidazol-2-yl)-4-phenol (PIMH) imprinted microspheres was prepared by suspension polymerization using 2-(2’-hydroxy-4-ethenylphenyl) imidazole as a functional monomer and ethylene glycol dimethacrylate as a crosslinker in the presence of various organonitrogen compounds (templates) to produce 2-(2’-hydroxy-4-ethenylphenyl) imidazole (PIMH). Imprinted microspheres show selectivity for various target model nitrogen-containing compounds with adsorption capacities of 6.8 ± 0.2 mg/g, 6.3 ± 0.3 mg/g and 5.8 ± 0.3 mg/g for quinoline, pyrimidine and carbazole, respectively. Adsorption selectivity increased in the order of quinoline (αi-r = 136.9) ˃ pyrimidine (αi-r = 126.2) ˃carbazole (αi-r = 86.3), when naphthalene was selected as a reference compound. Though, imprinted microspheres displayed excellent nitrogen compound removal both in model and real fuel, there was a need to improve the adsorbent adsorption capacity for N-compounds in fuel through the fabrication of imprinted nanofibers. Molecularly imprinted poly-2-(1H-imidazol-2-yl)-4-phenol nanofibers was prepared by electrospinning of 2-(2’-hydroxy-4-ethenylphenyl) imidazole (PIMH) in the presence of various organonitrogen compounds. These imprinted nanofibers show selectivity for various target model nitrogen-containing compounds with adsorption capacities of 11.7 ± 0.9 mg/g, 11.9 ± 0.8 mg/g and 11.3 ± 1.1 mg/g for quinoline, pyrimidine and carbazole, respectively. Adsorption selectivity increased in the order of pyrimidine (αi-r = 258.8) ˃ quinoline (αi-r = 235.5) ˃ carbazole (αi-r = 168.2). It further displayed excellent nitrogen removal in real fuel. The use of polybenzimidazole (PBI) nanofibers showed selective adsorption of organonitrogen compounds as imprinted sorbent also displayed high selectivity for their target model nitrogen-containing compounds with adsorption capacities of 11.4 ± 0.4 mg/g, 11.9 ± 0.2 mg/g and 10.9 ± 0.7 mg/g for quinoline, pyrimidine and carbazole respectively. Adsorption selectivity increased in the order of pyrimidine (αi-r = 241.5) ˃ quinoline (αi-r = 237.6) ˃ carbazole (αi-r = 170). Thermodynamic parameters obtained from isothermal titration calorimetry (ITC) revealed that quinoline-PIMH/PBI and pyrimidine-PIMH/PBI interactions are exothermic in nature, while carbazole-PIMH/PBI is endothermic in nature. DFT calculations indicated that π-π interactions/stacking and hydrogen bond interactions took place between N-compounds (carbazole, quinoline and pyrimidine) and adsorbent (PIMH and PBI). A significant reduction in the quantity of nitrogen containing compounds in hydrotreated fuel was observed (peak area reduction) when adsorbents (PIMH and PBI) was employed, however, the complex nature of organonitrogen compounds in fuel complicate the structure/function approach on MIPs for targeting these unwanted compounds.
- Full Text:
- Date Issued: 2018
The development of functionalized electrospun nanofibers for the control of pathogenic microorganisms in water.
- Authors: Kleyi, Phumelele Eldridge
- Date: 2014
- Subjects: Electrospinning , Nanofibers , Pathogenic microorganisms , Pathogenic microorganisms -- Detection , Drinking water -- Microbiology , Water quality -- Measurement , Imidazoles , Spectrum analysis , Anti-infective agents , Polymerization
- Language: English
- Type: Thesis , Doctoral , PhD
- Identifier: vital:4497 , http://hdl.handle.net/10962/d1013134
- Description: The thesis presents the development of functionalized electrospun nylon 6 nanofibers for the eradication of pathogenic microorganisms in drinking water. Imidazole derivatives were synthesized as the antimicrobial agents and were characterized by means of NMR spectroscopy, IR spectroscopy, elemental analysis and X-ray crystallography. The first set of compounds (2-substituted N-alkylimidazoles) consisted of imidazole derivatives substituted with different alkyl groups (methyl, ethyl, propyl, butyl, heptyl, octyl, decyl and benzyl) at the 1-position and various functional groups [carboxaldehyde (CHO), alcohol (CH2OH) and carboxylic acid (COOH)] at the 2-position. It was observed that the antimicrobial activity of the compounds increased with increasing alkyl chain length and decreasing pKa of the 2-substituent. It was also observed that the antimicrobial activity was predominantly against a Gram-positive bacterial strains [Staphylococcus aureus (MIC = 5-160 μg/mL) and Bacillus subtilis subsp. spizizenii (MIC = 5-20 μg/mL)], with the latter being the more susceptible. However, the compounds displayed poor antimicrobial activity against Gram-negative bacterial strain, E. coli (MIC = 150- >2500 μg/mL) and did not show any activity against the yeast, C. albicans. The second set of compounds consisted of the silver(I) complexes containing 2-hydroxymethyl-N-alkylimidazoles. The complexes displayed a broad spectrum antimicrobial activity towards the microorganisms that were tested and their activity [E. coli (MIC = 5-40 μg/mL), S. aureus (MIC = 20-80 μg/mL), Bacillus subtilis subsp. spizizenii (MIC = 5-40 μg/mL) and C. albicans (MIC = 40-80 μg/mL)] increased with the alkyl chain length of the 2-hydroxymethyl-N-alkylimidazole. The third set of compounds consisted of the vinylimidazoles containing the vinyl group either at the 1-position or at the 4- or 5- position. The imidazoles with the vinyl group at the 4- or 5-position contained the alkyl group (decyl) at the 1-position. For the fabrication of the antimicrobial nanofibers, the first two sets of imidazole derivatives (2-substituted N-alkylimidazoles and silver(I) complexes) were incorporated into electrospun nylon 6 nanofibers while the third set (2-substituted vinylimidazoles) was immobilized onto electrospun nylon 6 nanofibers employing the graft polymerization method. The antimicrobial nylon nanofibers were characterized by IR spectroscopy and SEM-EDAX (EDS). The electrospun nylon 6 nanofibers incorporated with 2-substituted N-alkylimidazoles displayed moderate to excellent levels of growth reduction against S. aureus (73.2-99.8 percent). For the electrospun nylon 6 nanofibers incorporated with silver(I) complexes, the levels of growth reduction were >99.99 percent, after the antimicrobial activity evaluation using the shake flask method. Furthermore, the grafted electrospun nylon 6 nanofibers showed excellent levels of growth reduction for E. coli (99.94-99.99 percent) and S. aureus (99.93-99.99 percent). The reusability results indicated that the grafted electrospun nylon 6 nanofibers maintained the antibacterial activity until the third cycle of useage. The cytotoxicity studies showed that grafted electrospun nylon 6 nanofibers possess lower cytotoxic effects on Chang liver cells with IC50 values in the range 23.48-26.81 μg/mL. The thesis demonstrated that the development of antimicrobial electrospun nanofibers, with potential for the eradication of pathogenic microoganisms in water, could be accomplished by incorporation as well as immobilization strategies.
- Full Text:
- Date Issued: 2014
- Authors: Kleyi, Phumelele Eldridge
- Date: 2014
- Subjects: Electrospinning , Nanofibers , Pathogenic microorganisms , Pathogenic microorganisms -- Detection , Drinking water -- Microbiology , Water quality -- Measurement , Imidazoles , Spectrum analysis , Anti-infective agents , Polymerization
- Language: English
- Type: Thesis , Doctoral , PhD
- Identifier: vital:4497 , http://hdl.handle.net/10962/d1013134
- Description: The thesis presents the development of functionalized electrospun nylon 6 nanofibers for the eradication of pathogenic microorganisms in drinking water. Imidazole derivatives were synthesized as the antimicrobial agents and were characterized by means of NMR spectroscopy, IR spectroscopy, elemental analysis and X-ray crystallography. The first set of compounds (2-substituted N-alkylimidazoles) consisted of imidazole derivatives substituted with different alkyl groups (methyl, ethyl, propyl, butyl, heptyl, octyl, decyl and benzyl) at the 1-position and various functional groups [carboxaldehyde (CHO), alcohol (CH2OH) and carboxylic acid (COOH)] at the 2-position. It was observed that the antimicrobial activity of the compounds increased with increasing alkyl chain length and decreasing pKa of the 2-substituent. It was also observed that the antimicrobial activity was predominantly against a Gram-positive bacterial strains [Staphylococcus aureus (MIC = 5-160 μg/mL) and Bacillus subtilis subsp. spizizenii (MIC = 5-20 μg/mL)], with the latter being the more susceptible. However, the compounds displayed poor antimicrobial activity against Gram-negative bacterial strain, E. coli (MIC = 150- >2500 μg/mL) and did not show any activity against the yeast, C. albicans. The second set of compounds consisted of the silver(I) complexes containing 2-hydroxymethyl-N-alkylimidazoles. The complexes displayed a broad spectrum antimicrobial activity towards the microorganisms that were tested and their activity [E. coli (MIC = 5-40 μg/mL), S. aureus (MIC = 20-80 μg/mL), Bacillus subtilis subsp. spizizenii (MIC = 5-40 μg/mL) and C. albicans (MIC = 40-80 μg/mL)] increased with the alkyl chain length of the 2-hydroxymethyl-N-alkylimidazole. The third set of compounds consisted of the vinylimidazoles containing the vinyl group either at the 1-position or at the 4- or 5- position. The imidazoles with the vinyl group at the 4- or 5-position contained the alkyl group (decyl) at the 1-position. For the fabrication of the antimicrobial nanofibers, the first two sets of imidazole derivatives (2-substituted N-alkylimidazoles and silver(I) complexes) were incorporated into electrospun nylon 6 nanofibers while the third set (2-substituted vinylimidazoles) was immobilized onto electrospun nylon 6 nanofibers employing the graft polymerization method. The antimicrobial nylon nanofibers were characterized by IR spectroscopy and SEM-EDAX (EDS). The electrospun nylon 6 nanofibers incorporated with 2-substituted N-alkylimidazoles displayed moderate to excellent levels of growth reduction against S. aureus (73.2-99.8 percent). For the electrospun nylon 6 nanofibers incorporated with silver(I) complexes, the levels of growth reduction were >99.99 percent, after the antimicrobial activity evaluation using the shake flask method. Furthermore, the grafted electrospun nylon 6 nanofibers showed excellent levels of growth reduction for E. coli (99.94-99.99 percent) and S. aureus (99.93-99.99 percent). The reusability results indicated that the grafted electrospun nylon 6 nanofibers maintained the antibacterial activity until the third cycle of useage. The cytotoxicity studies showed that grafted electrospun nylon 6 nanofibers possess lower cytotoxic effects on Chang liver cells with IC50 values in the range 23.48-26.81 μg/mL. The thesis demonstrated that the development of antimicrobial electrospun nanofibers, with potential for the eradication of pathogenic microoganisms in water, could be accomplished by incorporation as well as immobilization strategies.
- Full Text:
- Date Issued: 2014
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