Performance of magnetic nanocomposites for the removal of some selected contaminants from aqueous solution
- Authors: Ojemaye, Mike Onyewelehi
- Date: 2017
- Subjects: Nanocomposites (Materials)
- Language: English
- Type: Thesis , Doctoral , PhD
- Identifier: http://hdl.handle.net/10353/8746 , vital:33508
- Description: In this thesis, the performances of magnetic nanoparticles based materials were assessed for the removal or reduction of heavy metals in aqueous solutions. The successful synthesis of a novel adsorbent, azomethine functionalized magnetic nanoparticles (MNP-Maph) by covalent bonding between the amine group (-NH2) of amine functionalized magnetic nanoparticles (MNP-NH2) and carboxylic group (-COOH) of 4-{[(E)-phenylmethylidene]amino}benzoic acid (Maph-COOH) was achieved. This adsorbent was examined for the removal of di and trivalent ions (Cu2+, Zn2+, As3+, Pb2+ and Hg2+) from aqueous solutions. Also, magnetic photocatalyst with silica interlayer (NiFe2O4-SiO2-TiO2) was synthesized and employed for the reduction of Cr(VI) in aqueous solution. The photocatalytic reduction efficiency of this material was compared with that of magnetic titanium dioxide (NiFe2O4-TiO2) photocatalyst and titanium dioxide (TiO2) to ascertain the material with the best photocatalytic efficiency and ease of separation. All synthesized materials were characterized by using XRD, FT-IR, TEM, SEM, TGA and VSM before application. For the adsorption processes, the effects of pH, contact time, adsorbent dose and temperature were examined to ascertain the experimental condition necessary for the optimal removal of metal ions from solution. The data obtained from all experiments were fitted into four kinetic models; pseudo-first order, pseudo-second order, elovich and intra particle diffusion models to determine the mechanism involved in the adsorption of these di and trivalent ions while two isotherm models were employed in the adorption processes; these include: Langmuir and Freudlich models. Also, for the photocatalytic experiment, the effects of pH, contact time and photocatalyst dose were investigated to determine the experimental conditions necessary for the optimal reduction of Cr(VI) in aqueous solution. MNP-Maph showed excellent removal capacities of 34.08, 35.83, 50.08, 58.24 and 59.24 mg g-1 for Cu2+, Zn2+, As3+, Pb2+ and Hg2+ respectively compared to data previously reported in literature. This is as a result of the high affinity of azomethine group towards metal ions which tremendously enhanced removal of metal ions by adsorption. The incorporation of azomethine to magnetic nanoparticles improved the affinity towards metal ions removal forming strong electrostatic interaction between the adsorbent active sites and adsorbates. Also, the utilization of NiFe2O4-SiO2-TiO4, NiFe2O4-TiO2 and TiO2 for the reduction of Cr(VI) in aqueous solution showed a good photocatalytic performance with NiFe2O4-SiO2-TiO2 showing to be better in terms of both photocatalytic reduction and magnetic separation. TiO2 was observed to have 96.7percent reduction efficiency within 240 min while NiFe2O4-SiO2-TiO2 has 96.5percent reduction efficiency within 300 min and NiFe2O4-TiO2 gave 60percent reduction efficiency within 300 min of UV irradiation. This magnetic photocatalyst composite (NiFe2O4-SiO2-TiO2) gives the advantage of avoiding the problem of separation often encountered with most photocatalyst materials including TiO2 by allowing separation with the aid of a magnetic field. The adsorption processes were all described by pseudo-second order and Langmuir isotherm models while the photocatalytic process was described by Langmuir-Hinshelwood (L-H) kinetic model. Furthermore, thermodynamic experiment studied for the adsorption processes showed that all metal ion adsorption except Hg2+ by MNP-Maph were endothermic in nature, rapid and spontaneous indicating the feasibility of the sorbent material for the removal of metal ions from aqueous solutions. Also, regenerability study conducted to determine the reusability of sorbent material after seven cycles showed the potential to reuse sorbent material seven times or more. The reusability of the sorbent material was observed to show a percentage of an average of 78percent using 50:50 mixture of 0.1 mol dm-3 HNO3 and HCl for all adsorption processes. For the photocatalytic experiment, regenerability using 0.1 mol dm-3 for 1 h was observed to be very impressive after 3 runs for all synthesized photocatalytic materials. This thereby implies that the removal of metal ions by these materials will not in any way introduce secondary pollutants into the environment. Rather, it will avert the production of secondary pollutants. Also, the use of simple conventional chemicals for the regeneration of synthesized materials showed that regeneration in this study is cost effective as regeneration has been known to cost about three quarter of the total operation and maintenance of an adsorption or photocatalytic process. Application of MNP-Maph to real wastewater sampled from five different wastewater treatment plants in Eastern Cape Province for the removal of Cu2+, Zn2+ and As3+ showed that removal efficiencies of approximately 80 percent were achieved for all three metal ions upon adsorption by MNP-Maph. These therefore show that the introduction of metal loving ligand such as Maph-COOH improved the efficiency of MNP towards the removal of heavy metal ions from aqueous solution. Also, silica positively influenced the performance of magnetic titanium dioxide towards Cr(VI) reduction and separation from aqueous solution. This study therefore showed that these materials should be considered for future applications in the area of water/wastewater decontamination.
- Full Text:
- Date Issued: 2017
- Authors: Ojemaye, Mike Onyewelehi
- Date: 2017
- Subjects: Nanocomposites (Materials)
- Language: English
- Type: Thesis , Doctoral , PhD
- Identifier: http://hdl.handle.net/10353/8746 , vital:33508
- Description: In this thesis, the performances of magnetic nanoparticles based materials were assessed for the removal or reduction of heavy metals in aqueous solutions. The successful synthesis of a novel adsorbent, azomethine functionalized magnetic nanoparticles (MNP-Maph) by covalent bonding between the amine group (-NH2) of amine functionalized magnetic nanoparticles (MNP-NH2) and carboxylic group (-COOH) of 4-{[(E)-phenylmethylidene]amino}benzoic acid (Maph-COOH) was achieved. This adsorbent was examined for the removal of di and trivalent ions (Cu2+, Zn2+, As3+, Pb2+ and Hg2+) from aqueous solutions. Also, magnetic photocatalyst with silica interlayer (NiFe2O4-SiO2-TiO2) was synthesized and employed for the reduction of Cr(VI) in aqueous solution. The photocatalytic reduction efficiency of this material was compared with that of magnetic titanium dioxide (NiFe2O4-TiO2) photocatalyst and titanium dioxide (TiO2) to ascertain the material with the best photocatalytic efficiency and ease of separation. All synthesized materials were characterized by using XRD, FT-IR, TEM, SEM, TGA and VSM before application. For the adsorption processes, the effects of pH, contact time, adsorbent dose and temperature were examined to ascertain the experimental condition necessary for the optimal removal of metal ions from solution. The data obtained from all experiments were fitted into four kinetic models; pseudo-first order, pseudo-second order, elovich and intra particle diffusion models to determine the mechanism involved in the adsorption of these di and trivalent ions while two isotherm models were employed in the adorption processes; these include: Langmuir and Freudlich models. Also, for the photocatalytic experiment, the effects of pH, contact time and photocatalyst dose were investigated to determine the experimental conditions necessary for the optimal reduction of Cr(VI) in aqueous solution. MNP-Maph showed excellent removal capacities of 34.08, 35.83, 50.08, 58.24 and 59.24 mg g-1 for Cu2+, Zn2+, As3+, Pb2+ and Hg2+ respectively compared to data previously reported in literature. This is as a result of the high affinity of azomethine group towards metal ions which tremendously enhanced removal of metal ions by adsorption. The incorporation of azomethine to magnetic nanoparticles improved the affinity towards metal ions removal forming strong electrostatic interaction between the adsorbent active sites and adsorbates. Also, the utilization of NiFe2O4-SiO2-TiO4, NiFe2O4-TiO2 and TiO2 for the reduction of Cr(VI) in aqueous solution showed a good photocatalytic performance with NiFe2O4-SiO2-TiO2 showing to be better in terms of both photocatalytic reduction and magnetic separation. TiO2 was observed to have 96.7percent reduction efficiency within 240 min while NiFe2O4-SiO2-TiO2 has 96.5percent reduction efficiency within 300 min and NiFe2O4-TiO2 gave 60percent reduction efficiency within 300 min of UV irradiation. This magnetic photocatalyst composite (NiFe2O4-SiO2-TiO2) gives the advantage of avoiding the problem of separation often encountered with most photocatalyst materials including TiO2 by allowing separation with the aid of a magnetic field. The adsorption processes were all described by pseudo-second order and Langmuir isotherm models while the photocatalytic process was described by Langmuir-Hinshelwood (L-H) kinetic model. Furthermore, thermodynamic experiment studied for the adsorption processes showed that all metal ion adsorption except Hg2+ by MNP-Maph were endothermic in nature, rapid and spontaneous indicating the feasibility of the sorbent material for the removal of metal ions from aqueous solutions. Also, regenerability study conducted to determine the reusability of sorbent material after seven cycles showed the potential to reuse sorbent material seven times or more. The reusability of the sorbent material was observed to show a percentage of an average of 78percent using 50:50 mixture of 0.1 mol dm-3 HNO3 and HCl for all adsorption processes. For the photocatalytic experiment, regenerability using 0.1 mol dm-3 for 1 h was observed to be very impressive after 3 runs for all synthesized photocatalytic materials. This thereby implies that the removal of metal ions by these materials will not in any way introduce secondary pollutants into the environment. Rather, it will avert the production of secondary pollutants. Also, the use of simple conventional chemicals for the regeneration of synthesized materials showed that regeneration in this study is cost effective as regeneration has been known to cost about three quarter of the total operation and maintenance of an adsorption or photocatalytic process. Application of MNP-Maph to real wastewater sampled from five different wastewater treatment plants in Eastern Cape Province for the removal of Cu2+, Zn2+ and As3+ showed that removal efficiencies of approximately 80 percent were achieved for all three metal ions upon adsorption by MNP-Maph. These therefore show that the introduction of metal loving ligand such as Maph-COOH improved the efficiency of MNP towards the removal of heavy metal ions from aqueous solution. Also, silica positively influenced the performance of magnetic titanium dioxide towards Cr(VI) reduction and separation from aqueous solution. This study therefore showed that these materials should be considered for future applications in the area of water/wastewater decontamination.
- Full Text:
- Date Issued: 2017
Nanocomposites of carbon nanomaterials and metallophthalocyanines : applications towards electrocatalysis
- Authors: Nyoni, Stephen
- Date: 2016
- Subjects: Nanocomposites (Materials) , Nanostructured materials , Electrocatalysis
- Language: English
- Type: Thesis , Doctoral , PhD
- Identifier: vital:4561 , http://hdl.handle.net/10962/d1020846
- Description: Nanohybrid materials have been prepared and examined for their electrocatalytic activity. The nanocomposites have been prepared from carbon nanomaterials (multiwalled carbon nanotubes (MWCNTs) and graphene nanosheets), cadmium selenide quantum dots and metallophthalocyanines (MPcs). The MPcs used in this work are cobalt tetraamino-phthalocyanine (CoTAPc) and tetra (4-(4,6-diaminopyrimidin-2-ylthio) phthalocyaninatocobalt (II)) (CoPyPc). Their activity has also been explored in different forms; polymeric MPcs, iodine doped MPcs and covalently linked MPcs. The premixed drop-dry, sequential drop-dry and electropolymerisation electrode modification techniques were used to prepare nanocomposite catalysts on the glassy carbon electrode (GCE) surface. The sequential drop dry technique for MPc and MWCNTs gave better catalytic responses in terms of limit of detection, catalytic and electron transfer rate constants relative to the premixed. MWCNTs and CdSe-QDs have been used as intercalating agents to reduce restacking of graphene nanosheets during nanocomposite preparation. Voltammetry, chronoamperometry, scanning electrochemical microscopy and electrochemical impedance spectroscopy methods are used for electrochemical characterization modified GCE. X-ray photoelectron spectroscopy, X-ray diffractometry, transmission electron microscopy, scanning electron microscopy, infra-red spectroscopy, Raman spectroscopy were used to explore surface functionalities, morphology and topography of the nanocomposites. Electrocatalytic activity and possible applications of the modified electrodes were tested using oxygen reduction reaction, l-cysteine oxidation and paraquat reduction. Activity of nanocomposites was found superior over individual nanomaterials in these applications.
- Full Text:
- Date Issued: 2016
- Authors: Nyoni, Stephen
- Date: 2016
- Subjects: Nanocomposites (Materials) , Nanostructured materials , Electrocatalysis
- Language: English
- Type: Thesis , Doctoral , PhD
- Identifier: vital:4561 , http://hdl.handle.net/10962/d1020846
- Description: Nanohybrid materials have been prepared and examined for their electrocatalytic activity. The nanocomposites have been prepared from carbon nanomaterials (multiwalled carbon nanotubes (MWCNTs) and graphene nanosheets), cadmium selenide quantum dots and metallophthalocyanines (MPcs). The MPcs used in this work are cobalt tetraamino-phthalocyanine (CoTAPc) and tetra (4-(4,6-diaminopyrimidin-2-ylthio) phthalocyaninatocobalt (II)) (CoPyPc). Their activity has also been explored in different forms; polymeric MPcs, iodine doped MPcs and covalently linked MPcs. The premixed drop-dry, sequential drop-dry and electropolymerisation electrode modification techniques were used to prepare nanocomposite catalysts on the glassy carbon electrode (GCE) surface. The sequential drop dry technique for MPc and MWCNTs gave better catalytic responses in terms of limit of detection, catalytic and electron transfer rate constants relative to the premixed. MWCNTs and CdSe-QDs have been used as intercalating agents to reduce restacking of graphene nanosheets during nanocomposite preparation. Voltammetry, chronoamperometry, scanning electrochemical microscopy and electrochemical impedance spectroscopy methods are used for electrochemical characterization modified GCE. X-ray photoelectron spectroscopy, X-ray diffractometry, transmission electron microscopy, scanning electron microscopy, infra-red spectroscopy, Raman spectroscopy were used to explore surface functionalities, morphology and topography of the nanocomposites. Electrocatalytic activity and possible applications of the modified electrodes were tested using oxygen reduction reaction, l-cysteine oxidation and paraquat reduction. Activity of nanocomposites was found superior over individual nanomaterials in these applications.
- Full Text:
- Date Issued: 2016
Preparation and characterisation of nanocomposite biodegradable films of hake fish gelatine and Na-montmorillonite
- Authors: Mutize, Innocent
- Date: 2012-12
- Subjects: Nanocomposites (Materials) , Food -- Packaging
- Language: English
- Type: Master's theses , text
- Identifier: http://hdl.handle.net/10353/24261 , vital:62595
- Description: Hake fish (Merluccius paradoxus) based films were prepared using gelatine extracted from hake fish bones and skins. They were characterized using FTIR, TGA and XRD. Polyethylene glycol and distilled water were used as plasticizer and solvent respectively. Montmorillonite clay was also added to the film matrix at different concentration (1-13percent gelatine weight) to improve the films‟ functional properties. Fourier Transform Infrared (FTIR), Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis (SDS-PAGE) and Ultra Violet-Visible (UV-Vis) spectroscopy analysis were used to characterise gelatine extracted from hake fish bones and skins. The extraction time and temperature were varied between 30 mins to 120 mins and 45°C to 75°C respectively. The yields of the gelatines extracted at the stated conditions were calculated from the hydroxyproline content giving values of 30 to 39percent, 43 to 55percent and 50 to 57percent for extraction at 45°C, 60°C and 75°C respectively. The effect of polyethylene glycol content on the mechanical and barrier properties of hake fish gelatine films was also investigated. The addition of polyethylene glycol to the film solution increased the water vapour permeability from 0.0321 ± 0.0011 ng.m/m2.s.Pa to 0.0993 ± 0.0007 ng.m/m2.s.Pa between 5 and 35percent polyethylene glycol content and decreased tensile strength from 41.92 ± 2.17 MPa to 29.93 ± 0.17 MPa. Sodium treated Montmorillonite was incorporated in the hake fish gelatine film solution in order to assess the effect of Montmorillonite clay on the film mechanical, barrier and thermal properties. Hake fish gelatine-montmorillonite composite films were successfully prepared and characterized. X-ray Diffraction (XRD) and Fourier Transform Infrared (FTIR) analysis indicated that the Montmorillonite clay in the film matrices was in an exfoliated state. Water vapour permeability was reduced from 0.0312 ± 0.0016 ng.m/m2.s.Pa to 0.0081 ± 0.0001ng.m/m2.s.Pa and tensile strength improved from 29.93 ± 0.17MPa to 76.78 ± 1.13 MPa. , Thesis (MSc) -- Faculty of Science and Agriculture, 2012
- Full Text:
- Date Issued: 2012-12
- Authors: Mutize, Innocent
- Date: 2012-12
- Subjects: Nanocomposites (Materials) , Food -- Packaging
- Language: English
- Type: Master's theses , text
- Identifier: http://hdl.handle.net/10353/24261 , vital:62595
- Description: Hake fish (Merluccius paradoxus) based films were prepared using gelatine extracted from hake fish bones and skins. They were characterized using FTIR, TGA and XRD. Polyethylene glycol and distilled water were used as plasticizer and solvent respectively. Montmorillonite clay was also added to the film matrix at different concentration (1-13percent gelatine weight) to improve the films‟ functional properties. Fourier Transform Infrared (FTIR), Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis (SDS-PAGE) and Ultra Violet-Visible (UV-Vis) spectroscopy analysis were used to characterise gelatine extracted from hake fish bones and skins. The extraction time and temperature were varied between 30 mins to 120 mins and 45°C to 75°C respectively. The yields of the gelatines extracted at the stated conditions were calculated from the hydroxyproline content giving values of 30 to 39percent, 43 to 55percent and 50 to 57percent for extraction at 45°C, 60°C and 75°C respectively. The effect of polyethylene glycol content on the mechanical and barrier properties of hake fish gelatine films was also investigated. The addition of polyethylene glycol to the film solution increased the water vapour permeability from 0.0321 ± 0.0011 ng.m/m2.s.Pa to 0.0993 ± 0.0007 ng.m/m2.s.Pa between 5 and 35percent polyethylene glycol content and decreased tensile strength from 41.92 ± 2.17 MPa to 29.93 ± 0.17 MPa. Sodium treated Montmorillonite was incorporated in the hake fish gelatine film solution in order to assess the effect of Montmorillonite clay on the film mechanical, barrier and thermal properties. Hake fish gelatine-montmorillonite composite films were successfully prepared and characterized. X-ray Diffraction (XRD) and Fourier Transform Infrared (FTIR) analysis indicated that the Montmorillonite clay in the film matrices was in an exfoliated state. Water vapour permeability was reduced from 0.0312 ± 0.0016 ng.m/m2.s.Pa to 0.0081 ± 0.0001ng.m/m2.s.Pa and tensile strength improved from 29.93 ± 0.17MPa to 76.78 ± 1.13 MPa. , Thesis (MSc) -- Faculty of Science and Agriculture, 2012
- Full Text:
- Date Issued: 2012-12
Development of a visible light active, photo-catalytic and antimicrobial nanocomposite of titanium dioxide and silicon dioxide for water treatment
- Authors: Mungondori, Henry Heroe
- Date: 2012
- Subjects: Titanium dioxide , Silica , Catalysis , Nanocomposites (Materials) , Water -- Purification
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11335 , http://hdl.handle.net/10353/471 , Titanium dioxide , Silica , Catalysis , Nanocomposites (Materials) , Water -- Purification
- Description: The aim of this study was to prepare composite materials based on titanium dioxide (TiO2) and silicon dioxide (SiO2), and to evaluate their photo-catalytic and antimicrobial properties. Carbon and nitrogen doped TiO2nano-particles were prepared via a sol gel synthesis, which is a simple hydrolysis and condensation technique. In situ doping was carried out using glucose and urea as carbon and nitrogen sources respectively. Doping increased the spectral response of titanium dioxide photo-catalyst, allowing it to utilise the visible region which is much wider than the UV region (about 40 % of the solar spectrum), thus making it a more efficient photo-catalyst. The carbon and nitrogen doped TiO2-SiO2nano-particles were immobilized on glass support material to allow for easy separation of the spent photo-catalyst after the photo-degradation process. Tetraethyl orthosilicate (TEOS) was employed as both a binder and precursor for silicon dioxide. A mixture of TiO2 and TEOS in a 1:1 ratio was allowed to polymerize on a glass support which had been treated with hydrofluoric acid to introduce OH groups. The prepared photo-catalytic material was characterized by FT-IR, XRD, DRS, TEM, EDX, and BET analyses. Carbon was found to be more effective as a dopant than nitrogen. It brought about a band gap reduction of 0.30 eV and a BET surface area of 95.4 m2g-1 on the photo-catalyst as compared to a gap reduction of 0.2 eV and surface area of 52.2 m2g-1 for nitrogen doped TiO2. On the other hand, introduction of SiO2 allowed utilization of visible light by the TiO2-SiO2 nano-composite leading to an improved rate of photo-degradation of both methyl orange and phenol red. However, the immobilization of TiO2 on support material made it less effective towards inactivation of E. coli ATCC 25922 bacterial cells when compared to powdered TiO2 which was able to inactivate about 98 % of the bacterial cells within an hour of treatment.
- Full Text:
- Date Issued: 2012
- Authors: Mungondori, Henry Heroe
- Date: 2012
- Subjects: Titanium dioxide , Silica , Catalysis , Nanocomposites (Materials) , Water -- Purification
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11335 , http://hdl.handle.net/10353/471 , Titanium dioxide , Silica , Catalysis , Nanocomposites (Materials) , Water -- Purification
- Description: The aim of this study was to prepare composite materials based on titanium dioxide (TiO2) and silicon dioxide (SiO2), and to evaluate their photo-catalytic and antimicrobial properties. Carbon and nitrogen doped TiO2nano-particles were prepared via a sol gel synthesis, which is a simple hydrolysis and condensation technique. In situ doping was carried out using glucose and urea as carbon and nitrogen sources respectively. Doping increased the spectral response of titanium dioxide photo-catalyst, allowing it to utilise the visible region which is much wider than the UV region (about 40 % of the solar spectrum), thus making it a more efficient photo-catalyst. The carbon and nitrogen doped TiO2-SiO2nano-particles were immobilized on glass support material to allow for easy separation of the spent photo-catalyst after the photo-degradation process. Tetraethyl orthosilicate (TEOS) was employed as both a binder and precursor for silicon dioxide. A mixture of TiO2 and TEOS in a 1:1 ratio was allowed to polymerize on a glass support which had been treated with hydrofluoric acid to introduce OH groups. The prepared photo-catalytic material was characterized by FT-IR, XRD, DRS, TEM, EDX, and BET analyses. Carbon was found to be more effective as a dopant than nitrogen. It brought about a band gap reduction of 0.30 eV and a BET surface area of 95.4 m2g-1 on the photo-catalyst as compared to a gap reduction of 0.2 eV and surface area of 52.2 m2g-1 for nitrogen doped TiO2. On the other hand, introduction of SiO2 allowed utilization of visible light by the TiO2-SiO2 nano-composite leading to an improved rate of photo-degradation of both methyl orange and phenol red. However, the immobilization of TiO2 on support material made it less effective towards inactivation of E. coli ATCC 25922 bacterial cells when compared to powdered TiO2 which was able to inactivate about 98 % of the bacterial cells within an hour of treatment.
- Full Text:
- Date Issued: 2012
Photocatalytic activity and antibacterial properties of Ag/N-doped TiO2 nanoparticles on PVAE-CS nanofibre support
- Authors: Ocwelwang, Atsile Rosy
- Date: 2012
- Subjects: Nanocomposites (Materials) , Nanofibers , Electrospinning
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11337 , http://hdl.handle.net/10353/d1006794 , Nanocomposites (Materials) , Nanofibers , Electrospinning
- Description: Lack of potable water is one of the major challenges that the world faces currently and the effects of this are mainly experienced by people in developing countries. This has therefore propelled research in advanced oxidation technologies AOTs to improve the current water treatment methods using cost effective, non toxic and efficient treatment methods. Hence, in this study the sol-gel synthesis method was used to prepare TiO2 nanoparticles that were photocatalytically active under UV and visible solar light as well as possessing antibacterial properties. Silver and nitrogen doping was carried out to extend the optical absorption of TiO2. For easy removal and reuse of the photocatalyst the nanoparticles were immobilized on chitosan and poly (vinyl-alcohol-co-ethylene) using the electrospining technique. The synthesized nanomaterials were characterized by FTIR, XRD, SEM/EDS, TEM, DRS, and TGA. FTIR and EDS analysis confirmed the formation and composition of TiO2 nanopowders for the doped and undoped nanoparticles. XRD analysis showed that the anatase phase was the dominant crystalline phase of the synthesized nanopowders. SEM and TEM respectively illustrated the distribution and size of the electrospun nanofibers and the nanoparticles of TiO2. DRS results showed that there was a significant shift in the absorption band edge and wavelength of Ag-TiO2 to 397 nm, followed by N-TiO2 at 396 nm compared to the commercial titania which was at 359 nm. The photocatalytic activities and antibacterial properties of these materials were tested on methylene blue dye and E.coli microorganism respectively. Ag-TiO2 immobilized on nanofibers of chitosan and PVAE had the highest photocatalytic activity compared to N-TiO2. Similar results were observed when the biocide properties of these materials were tested on E. coli.
- Full Text:
- Date Issued: 2012
- Authors: Ocwelwang, Atsile Rosy
- Date: 2012
- Subjects: Nanocomposites (Materials) , Nanofibers , Electrospinning
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11337 , http://hdl.handle.net/10353/d1006794 , Nanocomposites (Materials) , Nanofibers , Electrospinning
- Description: Lack of potable water is one of the major challenges that the world faces currently and the effects of this are mainly experienced by people in developing countries. This has therefore propelled research in advanced oxidation technologies AOTs to improve the current water treatment methods using cost effective, non toxic and efficient treatment methods. Hence, in this study the sol-gel synthesis method was used to prepare TiO2 nanoparticles that were photocatalytically active under UV and visible solar light as well as possessing antibacterial properties. Silver and nitrogen doping was carried out to extend the optical absorption of TiO2. For easy removal and reuse of the photocatalyst the nanoparticles were immobilized on chitosan and poly (vinyl-alcohol-co-ethylene) using the electrospining technique. The synthesized nanomaterials were characterized by FTIR, XRD, SEM/EDS, TEM, DRS, and TGA. FTIR and EDS analysis confirmed the formation and composition of TiO2 nanopowders for the doped and undoped nanoparticles. XRD analysis showed that the anatase phase was the dominant crystalline phase of the synthesized nanopowders. SEM and TEM respectively illustrated the distribution and size of the electrospun nanofibers and the nanoparticles of TiO2. DRS results showed that there was a significant shift in the absorption band edge and wavelength of Ag-TiO2 to 397 nm, followed by N-TiO2 at 396 nm compared to the commercial titania which was at 359 nm. The photocatalytic activities and antibacterial properties of these materials were tested on methylene blue dye and E.coli microorganism respectively. Ag-TiO2 immobilized on nanofibers of chitosan and PVAE had the highest photocatalytic activity compared to N-TiO2. Similar results were observed when the biocide properties of these materials were tested on E. coli.
- Full Text:
- Date Issued: 2012
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