Comparison between base metals and platinum group metals in nitrogen, M codoped TiO 2 (M= Fe, Cu, Pd, Os) for photocatalytic removal of an organic dye in water
- Kuvarega, Alex T, Mamba, Bhekie B, Krause, Rui W M
- Authors: Kuvarega, Alex T , Mamba, Bhekie B , Krause, Rui W M
- Date: 2014
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/125129 , vital:35734 , https://doi.org/10.1155/2014/962102
- Description: The photocatalytic performance of a number of nonmetal and metal codoped TiO2 for the degradation of eosin yellow under simulated solar radiation was investigated. The synthesised materials were characterised by FTIR, Raman spectroscopy, XRD, DRUV-Vis, SEM, and TEM.The N, metal codoped TiO2 containing 0.5 wt.% of the metal consisted mainly of the anatase phase, with a particle size range of 15–28 nm. The particles were largely spherical and shifted the absorption edge well into the visible region. Band gap reduction was more pronounced for the N, PGM codoped TiO2 compared to N, base metal codoped samples. Codoping led to an enhancement in the photocatalytic activity of the materials for the degradation of eosin yellow. N, Pd codoped TiO2 was the most effective photocatalyst (99.9% dye removal) while N, Cu codoped TiO2 showed the least activity (25.5% removal). The mechanism for the photocatalytic enhancement was proposed on the basis of formation of an electron deficient Schottky barrier at the semiconductor-metal interface, which acts as an electron sink and thus retards electron-hole recombination. It was shown that the ability of the photocatalyst to degrade the dye depends on the nature and type of the metal dopant in the codoped TiO2 system.
- Full Text:
- Date Issued: 2014
- Authors: Kuvarega, Alex T , Mamba, Bhekie B , Krause, Rui W M
- Date: 2014
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/125129 , vital:35734 , https://doi.org/10.1155/2014/962102
- Description: The photocatalytic performance of a number of nonmetal and metal codoped TiO2 for the degradation of eosin yellow under simulated solar radiation was investigated. The synthesised materials were characterised by FTIR, Raman spectroscopy, XRD, DRUV-Vis, SEM, and TEM.The N, metal codoped TiO2 containing 0.5 wt.% of the metal consisted mainly of the anatase phase, with a particle size range of 15–28 nm. The particles were largely spherical and shifted the absorption edge well into the visible region. Band gap reduction was more pronounced for the N, PGM codoped TiO2 compared to N, base metal codoped samples. Codoping led to an enhancement in the photocatalytic activity of the materials for the degradation of eosin yellow. N, Pd codoped TiO2 was the most effective photocatalyst (99.9% dye removal) while N, Cu codoped TiO2 showed the least activity (25.5% removal). The mechanism for the photocatalytic enhancement was proposed on the basis of formation of an electron deficient Schottky barrier at the semiconductor-metal interface, which acts as an electron sink and thus retards electron-hole recombination. It was shown that the ability of the photocatalyst to degrade the dye depends on the nature and type of the metal dopant in the codoped TiO2 system.
- Full Text:
- Date Issued: 2014
Polyurethane composite adsorbent using solid phase extraction method for preconcentration of metal ion from aqueous solution
- Olorundare, O F, Msagati, T A M, Okonkwo, J O, Krause, Rui W M, Mamba, Bhekie B
- Authors: Olorundare, O F , Msagati, T A M , Okonkwo, J O , Krause, Rui W M , Mamba, Bhekie B
- Date: 2015
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/125386 , vital:35778 , https://doi.org/10.1007/s13762-014-0645-5
- Description: Polyurethane composite adsorbent polymeric material was prepared and investigated for selected solid-phase extraction for metal ions, prior to its determination by inductively coupled plasma optical emission spectrometry. The surface characterisation was done using Fourier transform infrared spectroscopy. The separation and preconcentration conditions of the analytes investigated includes influence of pH, sample loading flow rate, elution flow rate, type and concentration of eluents. The optimum pH for the highest efficient recoveries for all metal ions, which ranged from 70 to 85 %, is pH 7. The metal ions were quantitatively eluted with 5 mL of 2 mol/L HNO3. Common coexisting ions did not interfere with the separation. The percentage recovery of the metal ions ranged between 70 and 89 %, while the results for the limit of detection and limit of quantification ranged from 0.249 to 0.256 and 0.831 to 0.855, respectively. The experimental tests showed good preconcentration results of trace levels of metal ions using synthesised polyurethane polymer adsorbent composite.
- Full Text:
- Date Issued: 2015
- Authors: Olorundare, O F , Msagati, T A M , Okonkwo, J O , Krause, Rui W M , Mamba, Bhekie B
- Date: 2015
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/125386 , vital:35778 , https://doi.org/10.1007/s13762-014-0645-5
- Description: Polyurethane composite adsorbent polymeric material was prepared and investigated for selected solid-phase extraction for metal ions, prior to its determination by inductively coupled plasma optical emission spectrometry. The surface characterisation was done using Fourier transform infrared spectroscopy. The separation and preconcentration conditions of the analytes investigated includes influence of pH, sample loading flow rate, elution flow rate, type and concentration of eluents. The optimum pH for the highest efficient recoveries for all metal ions, which ranged from 70 to 85 %, is pH 7. The metal ions were quantitatively eluted with 5 mL of 2 mol/L HNO3. Common coexisting ions did not interfere with the separation. The percentage recovery of the metal ions ranged between 70 and 89 %, while the results for the limit of detection and limit of quantification ranged from 0.249 to 0.256 and 0.831 to 0.855, respectively. The experimental tests showed good preconcentration results of trace levels of metal ions using synthesised polyurethane polymer adsorbent composite.
- Full Text:
- Date Issued: 2015
Nanostructured β-cyclodextrin-hyperbranched polyethyleneimine (β-CD-HPEI) embedded in polysulfone membrane for the removal of humic acid from water
- Malinga, S P, Arotiba, O A, Mapolie, S F, Diallo, M S, Mamba, Bhekie B, Krause, Rui W M
- Authors: Malinga, S P , Arotiba, O A , Mapolie, S F , Diallo, M S , Mamba, Bhekie B , Krause, Rui W M
- Date: 2013
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/125119 , vital:35732 , https://doi.org/10.1080/01496395.2013.809108
- Description: The synthesis of a new β-cyclodextrin-hyperbranched polyethyleneimine (β-CD-HPEI)/polysulfone (PSf) membranes via interfacial polymerization of trimesoyl chloride and β-CD-HPEI is described in this paper. The membranes were characterized by atomic force microscopy (AFM), high resolution scanning electron microscopy (HR-SEM) and contact-angle measurements. Water permeability and rejection data were obtained using a cross-flow filtration system at 0.69 MPa. The membranes were hydrophilic (25° to 63°), showed high humic acid rejection (>amp;80%), and maintained a constant flux throughout the filtration. The modified membranes were rougher than the pristine PSf membranes but they exhibited better antifouling properties due to the hydrophilic surface which acted as a barrier against humic acid deposition. The modification of PSf with β-CD-HPEI resulted in enhanced hydrophilicity and water permeability while still maintaining high humic acid rejection. Supplemental materials are available for this article. Go to the publisher's online edition of Separation Science & Technology to view the supplemental file.
- Full Text:
- Date Issued: 2013
- Authors: Malinga, S P , Arotiba, O A , Mapolie, S F , Diallo, M S , Mamba, Bhekie B , Krause, Rui W M
- Date: 2013
- Language: English
- Type: text , article
- Identifier: http://hdl.handle.net/10962/125119 , vital:35732 , https://doi.org/10.1080/01496395.2013.809108
- Description: The synthesis of a new β-cyclodextrin-hyperbranched polyethyleneimine (β-CD-HPEI)/polysulfone (PSf) membranes via interfacial polymerization of trimesoyl chloride and β-CD-HPEI is described in this paper. The membranes were characterized by atomic force microscopy (AFM), high resolution scanning electron microscopy (HR-SEM) and contact-angle measurements. Water permeability and rejection data were obtained using a cross-flow filtration system at 0.69 MPa. The membranes were hydrophilic (25° to 63°), showed high humic acid rejection (>amp;80%), and maintained a constant flux throughout the filtration. The modified membranes were rougher than the pristine PSf membranes but they exhibited better antifouling properties due to the hydrophilic surface which acted as a barrier against humic acid deposition. The modification of PSf with β-CD-HPEI resulted in enhanced hydrophilicity and water permeability while still maintaining high humic acid rejection. Supplemental materials are available for this article. Go to the publisher's online edition of Separation Science & Technology to view the supplemental file.
- Full Text:
- Date Issued: 2013
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