Extraction, Isolation and Biological studies of Pentanisia prunelloides and Hippobromus pauciflorus
- Authors: Ngcetane , Lazola Luyolo
- Date: 2020
- Subjects: Medicinal plants Antioxidants
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: http://hdl.handle.net/10353/18766 , vital:42731
- Description: Enormous amounts of drugs or drug components have been found with the use and help of ethnobotanical knowledge of plants by the indigenous civilisation of that region. The primary reason that plants are chosen as a potential source of new medicines is that they are readily available to researcher and the public either free of charge or at a low and affordable cost in the rural majority community in the developing world. The aim of this study was to evaluate the chemical content of two commonly used medicinal plants of the Eastern Cape Province of South Africa and to explore their antioxidant potential. Crude extracts of Hippobromus pauciflorus and Pentanisia prunelloides were obtained by means of sequential solvent extraction followed by evaluation of the phenolic and flavonoid content of extracts and the anti-oxidant ability of the both plant samples and also their ability to hinder lipid peroxidation. For the H.pauciflorus sample, different masses of crude extracts were obtained with Dichloromethane (0.817 g) yielding the smallest mass and the 70% Ethanol (120.196 g) extract yielding the largest mass. The total phenolic content of the plant sample extracts were measured using the Folin-Ciocalteau reagent. The Methanol extract (133.019 ± 0.003 μgGAE/mL) exhibited the largest content while the EtOH extract (13.981 ± 0.001 μgGAE/mL) exhibited the least content. The MeOH extract exhibited the highest flavonoid content (46.005 ± 0.001 μgQE/mg extract) while the Hexane extract (19.000 ± 0.008 μgQE/mg extract) exhibited the least. 4 Final Submission of Thesis, Dissertation or Research Report/Project, Conference or Exam Paper Frap assay was performed with the Ethyl Acetate extract displaying the least anti-oxidant ability (10.284 ± 0.014 AAE/mL) while the Hex extract (204.705 ± 0.119 AAE/mL) displayed the highest anti-oxidant ability. 2, 2-diphenyl-1-picrylhydrazyl (DPPH) assay was performed with the hexane, methanol and ethanol extracts exhibiting an anti-oxidant property with IC50 values of 3.594x10-3 ± 0.133 mg/mL, 0.185 ± 0.019 mg/mL and 0.011 ± 0.002 mg/mL respectively. Inhibition of lipid peroxidation at 150 μg/mL was performed where the Dichloromethane extract showed the highest inhibition percentage (-75.000 ± 0.119%) while the Hex extract (-41.667 ± 0.021005%) showed the lowest inhibition percentage at 300 μg/mL; only the DCM extract (-3.051 ± 0.018%) displayed inhibition ability. For the P.prunelloides sample, different masses of crude extracts were obtained with EA extract (0.348 g) yielding the smallest mass and the MeOH (47.941 g) extract yielding the largest mass. Phenolic content was evaluated with the DCM extract (122.827 ± 0.010 μgGAE/mL) exhibited the largest content while the MeOH extract (48.788 ± 0.001 μgGAE/mL) exhibited the least content. Flavonoid content was evaluated with the DCM extract (88.543 ± 0.005 μgQE/mg extract) exhibited the largest content while the EtOH extract (19.254 ± 0.001 μgQE/mg extract) exhibited the least content. FRAP assay was performed with the DCM extract (13.021 ± 0.008 AAE/mL) displaying the least anti-oxidant ability while the MeOH extract (217.758 ± 0.025 AAE/mL) displaying the highest anti-oxidant ability. DPPH assay was conducted with EA and methanol extracts exhibiting antianti-oxidant ability and having IC50 values of 0.579 ± 0.021 mg/mL and 0.006± 0.001 mg/mL respectively. Inhibition of lipid peroxidation at 150 μg/mL was performed with the n-Hex extract (-36.395 ± 0.015%) showing the highest inhibition percentage while the DCM extract (-17.647 ± 0.005%) the lowest and at 300μg/mL the EA (- 12.881 ± 0.018%) and DCM (-0.847 ± 0.009%) extracts displayed inhibition. An attempt was made to isolate and elucidate the compounds in the extracts but unsuccessful, although the TLC results indicated several compounds that can be elucidated in future study
- Full Text:
- Date Issued: 2020
- Authors: Ngcetane , Lazola Luyolo
- Date: 2020
- Subjects: Medicinal plants Antioxidants
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: http://hdl.handle.net/10353/18766 , vital:42731
- Description: Enormous amounts of drugs or drug components have been found with the use and help of ethnobotanical knowledge of plants by the indigenous civilisation of that region. The primary reason that plants are chosen as a potential source of new medicines is that they are readily available to researcher and the public either free of charge or at a low and affordable cost in the rural majority community in the developing world. The aim of this study was to evaluate the chemical content of two commonly used medicinal plants of the Eastern Cape Province of South Africa and to explore their antioxidant potential. Crude extracts of Hippobromus pauciflorus and Pentanisia prunelloides were obtained by means of sequential solvent extraction followed by evaluation of the phenolic and flavonoid content of extracts and the anti-oxidant ability of the both plant samples and also their ability to hinder lipid peroxidation. For the H.pauciflorus sample, different masses of crude extracts were obtained with Dichloromethane (0.817 g) yielding the smallest mass and the 70% Ethanol (120.196 g) extract yielding the largest mass. The total phenolic content of the plant sample extracts were measured using the Folin-Ciocalteau reagent. The Methanol extract (133.019 ± 0.003 μgGAE/mL) exhibited the largest content while the EtOH extract (13.981 ± 0.001 μgGAE/mL) exhibited the least content. The MeOH extract exhibited the highest flavonoid content (46.005 ± 0.001 μgQE/mg extract) while the Hexane extract (19.000 ± 0.008 μgQE/mg extract) exhibited the least. 4 Final Submission of Thesis, Dissertation or Research Report/Project, Conference or Exam Paper Frap assay was performed with the Ethyl Acetate extract displaying the least anti-oxidant ability (10.284 ± 0.014 AAE/mL) while the Hex extract (204.705 ± 0.119 AAE/mL) displayed the highest anti-oxidant ability. 2, 2-diphenyl-1-picrylhydrazyl (DPPH) assay was performed with the hexane, methanol and ethanol extracts exhibiting an anti-oxidant property with IC50 values of 3.594x10-3 ± 0.133 mg/mL, 0.185 ± 0.019 mg/mL and 0.011 ± 0.002 mg/mL respectively. Inhibition of lipid peroxidation at 150 μg/mL was performed where the Dichloromethane extract showed the highest inhibition percentage (-75.000 ± 0.119%) while the Hex extract (-41.667 ± 0.021005%) showed the lowest inhibition percentage at 300 μg/mL; only the DCM extract (-3.051 ± 0.018%) displayed inhibition ability. For the P.prunelloides sample, different masses of crude extracts were obtained with EA extract (0.348 g) yielding the smallest mass and the MeOH (47.941 g) extract yielding the largest mass. Phenolic content was evaluated with the DCM extract (122.827 ± 0.010 μgGAE/mL) exhibited the largest content while the MeOH extract (48.788 ± 0.001 μgGAE/mL) exhibited the least content. Flavonoid content was evaluated with the DCM extract (88.543 ± 0.005 μgQE/mg extract) exhibited the largest content while the EtOH extract (19.254 ± 0.001 μgQE/mg extract) exhibited the least content. FRAP assay was performed with the DCM extract (13.021 ± 0.008 AAE/mL) displaying the least anti-oxidant ability while the MeOH extract (217.758 ± 0.025 AAE/mL) displaying the highest anti-oxidant ability. DPPH assay was conducted with EA and methanol extracts exhibiting antianti-oxidant ability and having IC50 values of 0.579 ± 0.021 mg/mL and 0.006± 0.001 mg/mL respectively. Inhibition of lipid peroxidation at 150 μg/mL was performed with the n-Hex extract (-36.395 ± 0.015%) showing the highest inhibition percentage while the DCM extract (-17.647 ± 0.005%) the lowest and at 300μg/mL the EA (- 12.881 ± 0.018%) and DCM (-0.847 ± 0.009%) extracts displayed inhibition. An attempt was made to isolate and elucidate the compounds in the extracts but unsuccessful, although the TLC results indicated several compounds that can be elucidated in future study
- Full Text:
- Date Issued: 2020
Fabrication of a photocatalytic PAN supported C-TiO2-CFA nanocomposite for use in water treatment
- Authors: Mpelane, Amkelwa
- Date: 2020
- Subjects: Photocatalysis
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: http://hdl.handle.net/10353/18744 , vital:42729
- Description: The goal of this study was to fabricate a visible light responsive composite of C-TiO2-CFA. The prepared nanocomposite (C-TiO2-CFA) was immobilized on poly(acrylonitrile) membrane to address the drawback of recovering the nanosized photocatalyst from water after photodegradation experiments. The C-TiO2-CFA nanocomposites were fabricated using a modified sol-gel method, while the C-TiO2-CFA/PAN membranes were prepared via the phase inversion technique. The nanocomposites were fully characterized using FTIR, XRD, SEM-EDX, TEM, DRS, and BET surface area analysis. The prepared C-TiO2-CFA/PAN membranes were evaluated in the photodegradation of methyl orange and the golden yellow dyes, as well as the photoreduction of lead and cadmium heavy metals in synthetic wastewater. UV-Visible spectroscopy was used to follow the changes in the concentration of organic dyes, while inductively coupled plasma optical emission spectroscopy was used to follow changes in the concentration of the heavy metals. FTIR analysis confirmed the presence of functional groups expected on the prepared C-TiO2- CFA/PAN membranes and EDX analysis accounted for the elements expected. The prepared membranes all exhibited an asymmetric structure as depicted by cross-sectional view study via SEM analysis. TEM and SEM analyses revealed that the prepared C-TiO2-CFA nanocomposite was roughly spherical in shape with an estimate particle size of 10.94 nm according to TEM and 11.62 nm according to XRD using Scherrer equation. The incorporation of carbon into the lattice structure of titanium dioxide resulted in a reduction in bandgap from 3.19 eV to 2.78 eV through introduction of mid-band states, allowing visible light utilization. The best nanocomposite was obtained by doping TiO2 with 4% carbon and having a C-TiO2 to CFA ratio of 4:1 respectively. The C-TiO2-CFA nanocomposite exhibits a crystalline structure with a mixture of rutile and anatase phases. The parameters investigated in the evaluation of photocatalytic performance of C-TiO2- CFA/PAN were effect of photocatalyst load on PAN membrane, initial dye concentration, pH and light source in the activation of photocatalyst. For both dyes (methyl arrange and golden yellow), it was observed that photodegradation efficiencies increased with an increase in catalyst load. In the photodegradation of MO and GY using the membrane with 1% C-TiO2- CFA, removal efficiencies of 73.3% and 59.99% were attained respectively, while the membrane with 2% C-TiO2-CFA achieved MO and GY photodegradation efficiencies of 99.8% and 99.2% respectively. Photodegradation efficiencies of MO and GY were observed to decrease with an increase in dye concentration. Low pH (3) was observed to favour the photodegradation of MO and GY azo dyes. Photodegradation efficiencies of 99.8% and 99.2% were attained where obtained at lower MO and GY initial concentration. The modified photocatalyst (C-TiO2-CFA/PAN) exhibited better photoactivity under sunlight irradiation compared to strict UV light irradiation. Evidently, the C-TiO2-CFA/PAN membranes can be 4 Final Submission of Thesis, Dissertation or Research Report/Project, Conference or Exam Paper utilized as a sustainable and stable photocatalyst to efficiently eliminate methyl orange and golden yellow dyes. A PAN membrane with 2 wt% C-TiO2-CFA revealed enhanced cadmium and lead removal efficiencies in comparison to PAN membranes with 1 wt% and 1.5% C-TiO2-CFA. A Cd2+ removal efficiency of 95% was obtained using 2 wt% C-TiO2-CFA/PAN nanocomposite membranes. Cadmium removal efficiencies of 92.5% and 91% were obtained using the 1.5 wt% and 1 wt% C-TiO2-CFA/PAN nanocomposite membranes. A lead removal efficiency of 97% was obtained using PAN membrane with 2 wt% C-TiO2-CFA. Pb2+ removal efficiencies of 90.9% and 94.6% were obtained using the 1.5 wt% and 1 wt% C-TiO2-CFA/PAN nanocomposite membranes. The photoreduction activity was observed to decrease with an increase in cadmium and lead initial concentrations. A cadmium and lead removal efficiencies of 95% and 97% were observed at lower Cd2+ and Pb2+ initial concentrations (20 ppm), respectively. The removal efficiencies varied marginally with changes in pH values. The fouling activity of the C-TiO2 modified PAN asymmetric membranes and pure PAN was investigated by carrying out pure water filtration tests as well as bovine serum albumin (BSA) filtration tests. A bovine serum albumin rejection of 98% was obtained utilizing the 2 wt% CTiO2-CFA/PAN membrane.
- Full Text:
- Date Issued: 2020
- Authors: Mpelane, Amkelwa
- Date: 2020
- Subjects: Photocatalysis
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: http://hdl.handle.net/10353/18744 , vital:42729
- Description: The goal of this study was to fabricate a visible light responsive composite of C-TiO2-CFA. The prepared nanocomposite (C-TiO2-CFA) was immobilized on poly(acrylonitrile) membrane to address the drawback of recovering the nanosized photocatalyst from water after photodegradation experiments. The C-TiO2-CFA nanocomposites were fabricated using a modified sol-gel method, while the C-TiO2-CFA/PAN membranes were prepared via the phase inversion technique. The nanocomposites were fully characterized using FTIR, XRD, SEM-EDX, TEM, DRS, and BET surface area analysis. The prepared C-TiO2-CFA/PAN membranes were evaluated in the photodegradation of methyl orange and the golden yellow dyes, as well as the photoreduction of lead and cadmium heavy metals in synthetic wastewater. UV-Visible spectroscopy was used to follow the changes in the concentration of organic dyes, while inductively coupled plasma optical emission spectroscopy was used to follow changes in the concentration of the heavy metals. FTIR analysis confirmed the presence of functional groups expected on the prepared C-TiO2- CFA/PAN membranes and EDX analysis accounted for the elements expected. The prepared membranes all exhibited an asymmetric structure as depicted by cross-sectional view study via SEM analysis. TEM and SEM analyses revealed that the prepared C-TiO2-CFA nanocomposite was roughly spherical in shape with an estimate particle size of 10.94 nm according to TEM and 11.62 nm according to XRD using Scherrer equation. The incorporation of carbon into the lattice structure of titanium dioxide resulted in a reduction in bandgap from 3.19 eV to 2.78 eV through introduction of mid-band states, allowing visible light utilization. The best nanocomposite was obtained by doping TiO2 with 4% carbon and having a C-TiO2 to CFA ratio of 4:1 respectively. The C-TiO2-CFA nanocomposite exhibits a crystalline structure with a mixture of rutile and anatase phases. The parameters investigated in the evaluation of photocatalytic performance of C-TiO2- CFA/PAN were effect of photocatalyst load on PAN membrane, initial dye concentration, pH and light source in the activation of photocatalyst. For both dyes (methyl arrange and golden yellow), it was observed that photodegradation efficiencies increased with an increase in catalyst load. In the photodegradation of MO and GY using the membrane with 1% C-TiO2- CFA, removal efficiencies of 73.3% and 59.99% were attained respectively, while the membrane with 2% C-TiO2-CFA achieved MO and GY photodegradation efficiencies of 99.8% and 99.2% respectively. Photodegradation efficiencies of MO and GY were observed to decrease with an increase in dye concentration. Low pH (3) was observed to favour the photodegradation of MO and GY azo dyes. Photodegradation efficiencies of 99.8% and 99.2% were attained where obtained at lower MO and GY initial concentration. The modified photocatalyst (C-TiO2-CFA/PAN) exhibited better photoactivity under sunlight irradiation compared to strict UV light irradiation. Evidently, the C-TiO2-CFA/PAN membranes can be 4 Final Submission of Thesis, Dissertation or Research Report/Project, Conference or Exam Paper utilized as a sustainable and stable photocatalyst to efficiently eliminate methyl orange and golden yellow dyes. A PAN membrane with 2 wt% C-TiO2-CFA revealed enhanced cadmium and lead removal efficiencies in comparison to PAN membranes with 1 wt% and 1.5% C-TiO2-CFA. A Cd2+ removal efficiency of 95% was obtained using 2 wt% C-TiO2-CFA/PAN nanocomposite membranes. Cadmium removal efficiencies of 92.5% and 91% were obtained using the 1.5 wt% and 1 wt% C-TiO2-CFA/PAN nanocomposite membranes. A lead removal efficiency of 97% was obtained using PAN membrane with 2 wt% C-TiO2-CFA. Pb2+ removal efficiencies of 90.9% and 94.6% were obtained using the 1.5 wt% and 1 wt% C-TiO2-CFA/PAN nanocomposite membranes. The photoreduction activity was observed to decrease with an increase in cadmium and lead initial concentrations. A cadmium and lead removal efficiencies of 95% and 97% were observed at lower Cd2+ and Pb2+ initial concentrations (20 ppm), respectively. The removal efficiencies varied marginally with changes in pH values. The fouling activity of the C-TiO2 modified PAN asymmetric membranes and pure PAN was investigated by carrying out pure water filtration tests as well as bovine serum albumin (BSA) filtration tests. A bovine serum albumin rejection of 98% was obtained utilizing the 2 wt% CTiO2-CFA/PAN membrane.
- Full Text:
- Date Issued: 2020
Preparation and characterization of sodium alginate-based dissolvable bandages as potential wound dressings
- Authors: Ndlovu, Sindi Prescila
- Date: 2020
- Subjects: Nanostructured materials
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: http://hdl.handle.net/10353/18800 , vital:42734
- Description: Burn wounds are among the leading causes of mortality and morbidity globally. Burn wounds are painful, cause social isolation and causes post-traumatic stress disorder (PTSD) due to prolonged hospital treatment. The challenges encountered in the treatment of burn wounds are infections resulting from the use of wound dressings that do not protect the wounds from microbial invasion. Sodium alginate-based dissolvable bandages were prepared and encapsulated with various antibiotics (ampicillin and ciprofloxacin) and nanoparticles (i.e. zinc oxide and silver). The dissolvable bandages were characterized by FTIR, SEM/EDX, TEM, XRD and TGA. Furthermore, the porosity, water uptake, biodegradation, antibacterial studies, and water vapour transmittance properties of the bandages were also studied. The prepared sodium alginate-based dissolvable bandage incorporated with varied amount of drugs (such as ampicillin, ciprofloxacin, zinc oxide and silver nanoparticle) exhibited good porosity, high water uptake, excellent WVTR with sustained drug release profiles. The loading of ZnO Nps, CLP/ZnO Nps and Ag Nps/CLP into the bandages improved the antibacterial activity of the bandages against both gram-negative and gram-positive strains of bacteria. XRD confirmed the amorphous nature of the dissolvable bandage and the absence of free drugs. FTIR revealed the successful encapsulation of the antibiotics and nanoparticle into the dissolvable bandages. The dissolvable bandages exhibited high water uptake ranging from 870-4468% with good porosity suggesting that they can absorb large amount of wound exudates. The drug release for all the bandages obeyed the Korsemeyer Peppas drug release model with n values in the range 0.1-1.0. The results obtained indicate that the bandages are potential wound dressings for burns and for patients with sensitive skins.
- Full Text:
- Date Issued: 2020
- Authors: Ndlovu, Sindi Prescila
- Date: 2020
- Subjects: Nanostructured materials
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: http://hdl.handle.net/10353/18800 , vital:42734
- Description: Burn wounds are among the leading causes of mortality and morbidity globally. Burn wounds are painful, cause social isolation and causes post-traumatic stress disorder (PTSD) due to prolonged hospital treatment. The challenges encountered in the treatment of burn wounds are infections resulting from the use of wound dressings that do not protect the wounds from microbial invasion. Sodium alginate-based dissolvable bandages were prepared and encapsulated with various antibiotics (ampicillin and ciprofloxacin) and nanoparticles (i.e. zinc oxide and silver). The dissolvable bandages were characterized by FTIR, SEM/EDX, TEM, XRD and TGA. Furthermore, the porosity, water uptake, biodegradation, antibacterial studies, and water vapour transmittance properties of the bandages were also studied. The prepared sodium alginate-based dissolvable bandage incorporated with varied amount of drugs (such as ampicillin, ciprofloxacin, zinc oxide and silver nanoparticle) exhibited good porosity, high water uptake, excellent WVTR with sustained drug release profiles. The loading of ZnO Nps, CLP/ZnO Nps and Ag Nps/CLP into the bandages improved the antibacterial activity of the bandages against both gram-negative and gram-positive strains of bacteria. XRD confirmed the amorphous nature of the dissolvable bandage and the absence of free drugs. FTIR revealed the successful encapsulation of the antibiotics and nanoparticle into the dissolvable bandages. The dissolvable bandages exhibited high water uptake ranging from 870-4468% with good porosity suggesting that they can absorb large amount of wound exudates. The drug release for all the bandages obeyed the Korsemeyer Peppas drug release model with n values in the range 0.1-1.0. The results obtained indicate that the bandages are potential wound dressings for burns and for patients with sensitive skins.
- Full Text:
- Date Issued: 2020
Synthesis and application of coal fly ash supported C doped TiO2/SnO2 photocatalyst in water treatment
- Authors: Sambakanya, Siyasanga
- Date: 2020
- Subjects: Photocatalysis
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: http://hdl.handle.net/10353/18838 , vital:42869
- Description: Coal fly ash supported carbon doped titanium dioxide/tin oxide (C doped TiO2-SnO2/CFA) nanoparticles were successfully synthesised using a sol gel method and calcined at 550 °C. The crystal structure, optical properties, morphology and other properties were analysed using XRD, UV-Vis, FTIR, TEM, SEM, DRS and EDX. SEM analysis showed that the nanoparticles (NPs) of C doped TiO2-SnO2/CFA were quasi spherical. XRD showed that C doped TiO2-SnO2/CFA nanoparticles were polycrystalline and consisted of both rutile and anatase phases. TEM analysis also displayed small NPs of C-TiO2-SnO2/CFA (12.62 nm) than TiO2 (16.19 nm) and SnO2 (19.98 nm). DRS revealed reduced band gap of C-TiO2 (2.78 eV) than TiO2 (3.19 eV) after doping. The photocatalytic efficiency of the prepared C-TiO2-SnO2/CFA nanoparticles was determined using methyl orange (MO) and methylene blue dye (MB) as standard dyes in the photodegradation as well as lead and mercury in the photoreduction of lead and mercury ions in water. The degradation experiments were carried under natural solar irradiation and UV light. The photodegradation experiments carried under visible light showed excellent photodegradation of MO & MB in water. This is a good indication that doping was successful as it imparted visible light activity in the C-TiO2-SnO2/CFA NPs. The photocatalyst efficiency was further tested while varying parameters including photocatalyst load, pH, and initial pollutant concentration in the photodegradation of MO & MB as well as in photoreduction of Pb2+ and Hg2+ in water to establish optimum operating conditions. The degradation rate of MO & MB increased when photocatalyst loading increased. When the pH was increased, the photocatalytic efficiency of the prepared photocatalyst towards methyl orange was reduced; however methylene blue degradation increased with increase in pH. The reduction of Pb2+ also increased with increasing pH whereas that of Hg2+ increased with decreasing pH. It was found that photodegradation was directly proportional to and photoreduction was inversely proportional to initial pollutant concentration.
- Full Text:
- Date Issued: 2020
- Authors: Sambakanya, Siyasanga
- Date: 2020
- Subjects: Photocatalysis
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: http://hdl.handle.net/10353/18838 , vital:42869
- Description: Coal fly ash supported carbon doped titanium dioxide/tin oxide (C doped TiO2-SnO2/CFA) nanoparticles were successfully synthesised using a sol gel method and calcined at 550 °C. The crystal structure, optical properties, morphology and other properties were analysed using XRD, UV-Vis, FTIR, TEM, SEM, DRS and EDX. SEM analysis showed that the nanoparticles (NPs) of C doped TiO2-SnO2/CFA were quasi spherical. XRD showed that C doped TiO2-SnO2/CFA nanoparticles were polycrystalline and consisted of both rutile and anatase phases. TEM analysis also displayed small NPs of C-TiO2-SnO2/CFA (12.62 nm) than TiO2 (16.19 nm) and SnO2 (19.98 nm). DRS revealed reduced band gap of C-TiO2 (2.78 eV) than TiO2 (3.19 eV) after doping. The photocatalytic efficiency of the prepared C-TiO2-SnO2/CFA nanoparticles was determined using methyl orange (MO) and methylene blue dye (MB) as standard dyes in the photodegradation as well as lead and mercury in the photoreduction of lead and mercury ions in water. The degradation experiments were carried under natural solar irradiation and UV light. The photodegradation experiments carried under visible light showed excellent photodegradation of MO & MB in water. This is a good indication that doping was successful as it imparted visible light activity in the C-TiO2-SnO2/CFA NPs. The photocatalyst efficiency was further tested while varying parameters including photocatalyst load, pH, and initial pollutant concentration in the photodegradation of MO & MB as well as in photoreduction of Pb2+ and Hg2+ in water to establish optimum operating conditions. The degradation rate of MO & MB increased when photocatalyst loading increased. When the pH was increased, the photocatalytic efficiency of the prepared photocatalyst towards methyl orange was reduced; however methylene blue degradation increased with increase in pH. The reduction of Pb2+ also increased with increasing pH whereas that of Hg2+ increased with decreasing pH. It was found that photodegradation was directly proportional to and photoreduction was inversely proportional to initial pollutant concentration.
- Full Text:
- Date Issued: 2020
Remediation of metal ions in aqueous solution using activated carbon from Zea may stem
- Authors: Matandabuzo, Mzukisi
- Date: 2016
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11360 , http://hdl.handle.net/10353/d1021328
- Description: Zea mays stem and its activated carbon were prepared through chemical activation method using four different activating reagents (NaOH, H₃PO₄, H₂SO₄, KOH) and were used as adsorbents for the removal of Pb(II), Cu(II), Hg(II) and Cr(III) from aqueous solution. The results shows that activated carbon has high surface area and pore volume compared to the powdered raw Zea mays stem. Prepared activated carbon was characterized using physico-chemical properties such as carbon yield, iodine number, moisture content, percentage adsorption, and analytical instruments such as Fourier transform Infrared spectroscopy (FTIR), atomic absorption spectrometer (AAS), scanning electron microscopy (SEM), Energy Dispersive X-ray analysis (EDS), powder X-ray Diffraction (pXRD). The adsorption of Pb(II), Cu(II), and Cr(III) ions were pH, contact time, and concentration dependent. Based on the results obtained from the batch experiments, activated carbon prepared from Zea mays stem is not good enough for the removal of Hg(II) from aqueous solution. Adsorption ability was calculated and found to be 66.67% for activated carbon obtained from H₂SO₄, 21.21% for activated carbon obtained from KOH, and 20% for activated carbons obtained from NaOH and H₃PO₄. The pH 5-6 was chosen for all experiments, contact time was 2 hours, and adsorbent dosage was 2 g, initial concentration range from 200, 400, 600, 800, and 1000 ppm at room temperature. The metal ion removal trend was found in the order Pb(II)>Cu(II)>Cr(III)>>Hg(II). The Langmuir model fitted well in most of the cases with > 0.99. Consequently, the adsorption of Pb(II) and Cu(II) followed Langmuir isotherm model while that of Cr(III) best fitted the Freundlich isotherm model. The results indicated that the adsorption process followed two possible mechanisms. (I) Metal ion – adsorbent complex model and (II) Metal ion – ion-exchange adsorbent complex model.
- Full Text:
- Date Issued: 2016
- Authors: Matandabuzo, Mzukisi
- Date: 2016
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11360 , http://hdl.handle.net/10353/d1021328
- Description: Zea mays stem and its activated carbon were prepared through chemical activation method using four different activating reagents (NaOH, H₃PO₄, H₂SO₄, KOH) and were used as adsorbents for the removal of Pb(II), Cu(II), Hg(II) and Cr(III) from aqueous solution. The results shows that activated carbon has high surface area and pore volume compared to the powdered raw Zea mays stem. Prepared activated carbon was characterized using physico-chemical properties such as carbon yield, iodine number, moisture content, percentage adsorption, and analytical instruments such as Fourier transform Infrared spectroscopy (FTIR), atomic absorption spectrometer (AAS), scanning electron microscopy (SEM), Energy Dispersive X-ray analysis (EDS), powder X-ray Diffraction (pXRD). The adsorption of Pb(II), Cu(II), and Cr(III) ions were pH, contact time, and concentration dependent. Based on the results obtained from the batch experiments, activated carbon prepared from Zea mays stem is not good enough for the removal of Hg(II) from aqueous solution. Adsorption ability was calculated and found to be 66.67% for activated carbon obtained from H₂SO₄, 21.21% for activated carbon obtained from KOH, and 20% for activated carbons obtained from NaOH and H₃PO₄. The pH 5-6 was chosen for all experiments, contact time was 2 hours, and adsorbent dosage was 2 g, initial concentration range from 200, 400, 600, 800, and 1000 ppm at room temperature. The metal ion removal trend was found in the order Pb(II)>Cu(II)>Cr(III)>>Hg(II). The Langmuir model fitted well in most of the cases with > 0.99. Consequently, the adsorption of Pb(II) and Cu(II) followed Langmuir isotherm model while that of Cr(III) best fitted the Freundlich isotherm model. The results indicated that the adsorption process followed two possible mechanisms. (I) Metal ion – adsorbent complex model and (II) Metal ion – ion-exchange adsorbent complex model.
- Full Text:
- Date Issued: 2016
Synthesis and structural studies of NiS and PdS nanoparticles/nanocomposites from dithiocarbamates single source precursors
- Authors: Nqombolo, Azile
- Date: 2016
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11359 , http://hdl.handle.net/10353/d1021326
- Description: The main aim of this research is to synthesize Ni(II) and Pd(II) dithiocarbamate complexes and use them as single source precursors for the synthesis of NiS and PdS nanoparticles and metal sulphides potato starch nanocomposites. Four dithiocarbamate ligands were synthesized and characterized using elemental analysis and spectroscopic techniques. The ligands were used to prepared homoleptic Ni(II) and Pd(II) complexes of the dithiocarbamate ligands. The metal complexes were characterized with elemental analysis, UV-Vis, FTIR and 1H-NMR spectroscopic techniques. Conductivity measurements indicate that all the complexes are non-electrolytes in solution and results from the electronic spectra studies confirmed the proposed 4-coordinate square planar geometry around the metal ions. The nickel complexes showed d-d transitions around 477 nm while in the palladium complexes, no d-d transitions were observed but the compounds showed strong metal to ligand charge transfer transitions. From the FTIR spectra studies, it can be confirmed that the complexes were successfully synthesised because all peaks of interest were observed at expected regions from the literature. The νC-N was observed around 1469-1495 cm-1, νC=S around 1101-1188 cm-1 and νC-S around 738-1060 cm-1 for both Ni(II) and Pd(II) complexes. νNi-S was observed around 375-543 cm-1 and νPd-S around 529-545 cm-1. The FTIR also confirmed that the dithiocarbamate ligands act as bidentate chelating ligands through the sulfur atoms. The complexes were used as single source precursors and thermolysed in hexadecylamine (HDA) at 220 °C to prepare four HDA-capped nickel sulfide nanoparticles and four palladium sulfide nanoparticles. The as-prepared nanoparticles were studied with optical absorption spectra, photoluminescence, powder X-ray diffraction (PXRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). The optical studies results showed that NiS have large band gaps that are greater than that of the bulk, therefore they are found to be blue shifted relative to the bulk, which shows that they have small particle size and thus confirming their quantum confinement effect. PL spectra reveal that the emission peaks are red shifted compared to the absorption band edges of the nanoparticles. The XRD patterns confirmed the formation of cubic and rhombohedral phase for NiS nanoparticles and cubic phase for PdS nanoparticles. SEM images of both NiS and PdS show uniform surface morphology at low and high magnification with different shapes. EDS analyses confirmed the presence of Ni, S, and Pd in each of the spectrum indicating that the nanoparticles were successfully synthesized. TEM images showed that the synthesised nanoparticles have uniform and narrow size distribution with no agglomeration. The sizes of the NiS nanoparticles were found to be in the range of 12-38 nm for NiS1, 8-11 nm for NiS2, 9-16 nm for NiS3 and 4-9 nm for NiS4. The TEM images for the as-prepared PdS nanoparticles showed that the average crystallite sizes are 6.94-9.62 nm for PdS1, 8-11 nm for PdS2, 9-16 nm for PdS3 and 4-9 nm for PdS4 respectively. The nanoparticles were used to prepare potato starch nanocomposites and SEM images indicate that the surface morphology of starch polymer nanocomposites compose of potato starch and few particles in between the pores of the matrix, this is due to the small ratio of nanoparticles used.
- Full Text:
- Date Issued: 2016
- Authors: Nqombolo, Azile
- Date: 2016
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11359 , http://hdl.handle.net/10353/d1021326
- Description: The main aim of this research is to synthesize Ni(II) and Pd(II) dithiocarbamate complexes and use them as single source precursors for the synthesis of NiS and PdS nanoparticles and metal sulphides potato starch nanocomposites. Four dithiocarbamate ligands were synthesized and characterized using elemental analysis and spectroscopic techniques. The ligands were used to prepared homoleptic Ni(II) and Pd(II) complexes of the dithiocarbamate ligands. The metal complexes were characterized with elemental analysis, UV-Vis, FTIR and 1H-NMR spectroscopic techniques. Conductivity measurements indicate that all the complexes are non-electrolytes in solution and results from the electronic spectra studies confirmed the proposed 4-coordinate square planar geometry around the metal ions. The nickel complexes showed d-d transitions around 477 nm while in the palladium complexes, no d-d transitions were observed but the compounds showed strong metal to ligand charge transfer transitions. From the FTIR spectra studies, it can be confirmed that the complexes were successfully synthesised because all peaks of interest were observed at expected regions from the literature. The νC-N was observed around 1469-1495 cm-1, νC=S around 1101-1188 cm-1 and νC-S around 738-1060 cm-1 for both Ni(II) and Pd(II) complexes. νNi-S was observed around 375-543 cm-1 and νPd-S around 529-545 cm-1. The FTIR also confirmed that the dithiocarbamate ligands act as bidentate chelating ligands through the sulfur atoms. The complexes were used as single source precursors and thermolysed in hexadecylamine (HDA) at 220 °C to prepare four HDA-capped nickel sulfide nanoparticles and four palladium sulfide nanoparticles. The as-prepared nanoparticles were studied with optical absorption spectra, photoluminescence, powder X-ray diffraction (PXRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). The optical studies results showed that NiS have large band gaps that are greater than that of the bulk, therefore they are found to be blue shifted relative to the bulk, which shows that they have small particle size and thus confirming their quantum confinement effect. PL spectra reveal that the emission peaks are red shifted compared to the absorption band edges of the nanoparticles. The XRD patterns confirmed the formation of cubic and rhombohedral phase for NiS nanoparticles and cubic phase for PdS nanoparticles. SEM images of both NiS and PdS show uniform surface morphology at low and high magnification with different shapes. EDS analyses confirmed the presence of Ni, S, and Pd in each of the spectrum indicating that the nanoparticles were successfully synthesized. TEM images showed that the synthesised nanoparticles have uniform and narrow size distribution with no agglomeration. The sizes of the NiS nanoparticles were found to be in the range of 12-38 nm for NiS1, 8-11 nm for NiS2, 9-16 nm for NiS3 and 4-9 nm for NiS4. The TEM images for the as-prepared PdS nanoparticles showed that the average crystallite sizes are 6.94-9.62 nm for PdS1, 8-11 nm for PdS2, 9-16 nm for PdS3 and 4-9 nm for PdS4 respectively. The nanoparticles were used to prepare potato starch nanocomposites and SEM images indicate that the surface morphology of starch polymer nanocomposites compose of potato starch and few particles in between the pores of the matrix, this is due to the small ratio of nanoparticles used.
- Full Text:
- Date Issued: 2016
Investigation into the characteristics and possible applications of biomass gasification by-products from a downdraft gasifier system
- Authors: Melapi, Aviwe
- Date: 2015
- Subjects: Biomass gasification -- South Africa -- Eastern Cape , Renewable energy sources -- South Africa -- Eastern Cape , Biomass energy -- South Africa -- Eastern Cape , Crop residue management -- South Africa -- Eastern Cape , Coal gasification -- South Africa -- Eastern Cape , Lignocellulose -- Biodegradation -- South Africa -- Eastern Cape
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11348 , http://hdl.handle.net/10353/d1020174 , Biomass gasification -- South Africa -- Eastern Cape , Renewable energy sources -- South Africa -- Eastern Cape , Biomass energy -- South Africa -- Eastern Cape , Crop residue management -- South Africa -- Eastern Cape , Coal gasification -- South Africa -- Eastern Cape , Lignocellulose -- Biodegradation -- South Africa -- Eastern Cape
- Description: Biomass gasification has attracted the interest of researchers because it produces zero carbon to the atmosphere. This technology does not only produce syngas but also the byproducts which can be used for various application depending on quality.The study conducted at Melani village in Alice in the Eastern Cape of South Africa was aimed at investigating the possible applications of the gasification byproducts instead of being thrown away. Pine wood was employed as the parent feedstock material for the gasifier. Biomass gasification by-products were then collected for further analysis. The studied by-products included tar(condensate), char, soot and resin. These materials were also blended to produce strong materials.The essence of the blending was to generate ideal material that is strong but light at the same time.The elemental analysis of the samples performed by CHNS analyser revealed that carbon element is in large quantities in all samples. The FTIR spectra showed almost similar results for all the studied samples, since the samples are end products of lignocellulosegasification. SEM gave the sticky images of resin as well as porous char structures. Char showed a higher heating value of 35.37MJ/Kg when compared to other by-products samples.
- Full Text:
- Date Issued: 2015
- Authors: Melapi, Aviwe
- Date: 2015
- Subjects: Biomass gasification -- South Africa -- Eastern Cape , Renewable energy sources -- South Africa -- Eastern Cape , Biomass energy -- South Africa -- Eastern Cape , Crop residue management -- South Africa -- Eastern Cape , Coal gasification -- South Africa -- Eastern Cape , Lignocellulose -- Biodegradation -- South Africa -- Eastern Cape
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11348 , http://hdl.handle.net/10353/d1020174 , Biomass gasification -- South Africa -- Eastern Cape , Renewable energy sources -- South Africa -- Eastern Cape , Biomass energy -- South Africa -- Eastern Cape , Crop residue management -- South Africa -- Eastern Cape , Coal gasification -- South Africa -- Eastern Cape , Lignocellulose -- Biodegradation -- South Africa -- Eastern Cape
- Description: Biomass gasification has attracted the interest of researchers because it produces zero carbon to the atmosphere. This technology does not only produce syngas but also the byproducts which can be used for various application depending on quality.The study conducted at Melani village in Alice in the Eastern Cape of South Africa was aimed at investigating the possible applications of the gasification byproducts instead of being thrown away. Pine wood was employed as the parent feedstock material for the gasifier. Biomass gasification by-products were then collected for further analysis. The studied by-products included tar(condensate), char, soot and resin. These materials were also blended to produce strong materials.The essence of the blending was to generate ideal material that is strong but light at the same time.The elemental analysis of the samples performed by CHNS analyser revealed that carbon element is in large quantities in all samples. The FTIR spectra showed almost similar results for all the studied samples, since the samples are end products of lignocellulosegasification. SEM gave the sticky images of resin as well as porous char structures. Char showed a higher heating value of 35.37MJ/Kg when compared to other by-products samples.
- Full Text:
- Date Issued: 2015
Ni(II) and Pb(II) dithiocarbamate complexes as precursors for the synthesis of HDA-capped NiS and PbS nanoparticles
- Authors: Chintso, Thobani
- Date: 2015
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11349 , http://hdl.handle.net/10353/d1020201
- Description: Ni(II) and Pb(II) dithiocarbamate complexes were synthesized and characterized by elemental analysis, UV-Vis, FTIR and TGA and some of the Ni(II) complexes and one Pb(II) were further analyzed by 1H-NMR and 13C-NMR spectroscopy. Generally all the dithiocarbamate ligands are soluble in water while the complexes were soluble mostly in solvents such as chloroform, toluene, DMSO and DCM. Based on the elemental analysis, the dithiocarbamate complexes are formulated as four coordinate (tetrahedral or square planar) compounds. However, the FTIR showed that each of the dithiocarbamate ligands acted as bidentate ligand through two sulfur atoms. The TGA of the most complexes showed one major decomposition step to give respective metal sulfide above 200 oC. In this research project, dithiocarbamate complexes were used as single source precursor for the synthesis of metal sulfide nanoparticles. We studied the optical and structural properties of metal sulfide nanoparticles using UV-Vis, photoluminescence (PL), powder X-ray diffraction (XRD), energy dispersive X-ray (EDX), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The absorption spectra of the metal sulfide nanoparticles are blue shifted in respect to bulk material and they also showed broad emission. The XRD of the NiS nanoparticles were indexed to the cubic and rhombohedral phase, with crystallite sizes of 15 - 18 nm. The XRD of PbS nanoparticles were indexed to the face centered cubic and cubic rock salts, with the crystallite sizes 12 - 18 nm. The TEM images of the metal sulfide nanoparticles showed particles with spherical and rectangular shapes with crystallite sizes 4 - 35 nm.
- Full Text:
- Date Issued: 2015
- Authors: Chintso, Thobani
- Date: 2015
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11349 , http://hdl.handle.net/10353/d1020201
- Description: Ni(II) and Pb(II) dithiocarbamate complexes were synthesized and characterized by elemental analysis, UV-Vis, FTIR and TGA and some of the Ni(II) complexes and one Pb(II) were further analyzed by 1H-NMR and 13C-NMR spectroscopy. Generally all the dithiocarbamate ligands are soluble in water while the complexes were soluble mostly in solvents such as chloroform, toluene, DMSO and DCM. Based on the elemental analysis, the dithiocarbamate complexes are formulated as four coordinate (tetrahedral or square planar) compounds. However, the FTIR showed that each of the dithiocarbamate ligands acted as bidentate ligand through two sulfur atoms. The TGA of the most complexes showed one major decomposition step to give respective metal sulfide above 200 oC. In this research project, dithiocarbamate complexes were used as single source precursor for the synthesis of metal sulfide nanoparticles. We studied the optical and structural properties of metal sulfide nanoparticles using UV-Vis, photoluminescence (PL), powder X-ray diffraction (XRD), energy dispersive X-ray (EDX), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The absorption spectra of the metal sulfide nanoparticles are blue shifted in respect to bulk material and they also showed broad emission. The XRD of the NiS nanoparticles were indexed to the cubic and rhombohedral phase, with crystallite sizes of 15 - 18 nm. The XRD of PbS nanoparticles were indexed to the face centered cubic and cubic rock salts, with the crystallite sizes 12 - 18 nm. The TEM images of the metal sulfide nanoparticles showed particles with spherical and rectangular shapes with crystallite sizes 4 - 35 nm.
- Full Text:
- Date Issued: 2015
Synthesis and characterization of Ru(II) phenyl-3-indenylidene olefin metathesis type complexes
- Authors: Yalezo, Ntsikelelo
- Date: 2015
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11351 , http://hdl.handle.net/10353/d1021128
- Description: In this study, a series of Ru(II) phenyl-3-indenylidene complexes with general formula of [RuCl2(NHC)(Ind)(L)] (where L= triphenylphosphine, pyridine and NHC = five different types of N-heterocyclic carbene ligands), have been synthesized and characterized using FT-IR, UV-Vis, elementally analysis and melting/decomposition point. The N,N’-diarylimidazolinium chlorides have been used as N-heterocyclic carbene precursors and were synthesized from their corresponding N,N’-diarylformamidines and further characterized using 1H-NMR, 13C-NMR, FTIR and melting point determination. The infrared spectra of the N,N’-diarylimidazolinium chlorides show a quaternary nature (R2N=C+) with broad vibration band in region 3300-3400 cm-1. The disappearance of this vibration band in the infrared spectra of the ruthenium(II) complexes was used to confirm the coordination of the ligand to the ruthenium ions. The percentage analysis of carbon, hydrogen and nitrogen obtained corresponded with the calculated percentages of these atoms in the complexes with the slight difference of less than 1%. The electronic spectra of the complexes show three distinct absorption bands. The two bands are due to intraligand charge transfers transition assigned to π→π*, n→π* and third band is due to d-d transition, signifying the presence of the metal ion. The synthesized Ru(II) complexes did not show any of melting, however a change in colour was observed signifying the decomposition of the complexes.
- Full Text:
- Date Issued: 2015
- Authors: Yalezo, Ntsikelelo
- Date: 2015
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11351 , http://hdl.handle.net/10353/d1021128
- Description: In this study, a series of Ru(II) phenyl-3-indenylidene complexes with general formula of [RuCl2(NHC)(Ind)(L)] (where L= triphenylphosphine, pyridine and NHC = five different types of N-heterocyclic carbene ligands), have been synthesized and characterized using FT-IR, UV-Vis, elementally analysis and melting/decomposition point. The N,N’-diarylimidazolinium chlorides have been used as N-heterocyclic carbene precursors and were synthesized from their corresponding N,N’-diarylformamidines and further characterized using 1H-NMR, 13C-NMR, FTIR and melting point determination. The infrared spectra of the N,N’-diarylimidazolinium chlorides show a quaternary nature (R2N=C+) with broad vibration band in region 3300-3400 cm-1. The disappearance of this vibration band in the infrared spectra of the ruthenium(II) complexes was used to confirm the coordination of the ligand to the ruthenium ions. The percentage analysis of carbon, hydrogen and nitrogen obtained corresponded with the calculated percentages of these atoms in the complexes with the slight difference of less than 1%. The electronic spectra of the complexes show three distinct absorption bands. The two bands are due to intraligand charge transfers transition assigned to π→π*, n→π* and third band is due to d-d transition, signifying the presence of the metal ion. The synthesized Ru(II) complexes did not show any of melting, however a change in colour was observed signifying the decomposition of the complexes.
- Full Text:
- Date Issued: 2015
Synthesis, characterisation and evaluation of functionalized Lignocelluloses-clay nanocomposites for organic pollutant removal from water
- Authors: Mafukidze, Donovan M
- Date: 2015
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11356 , http://hdl.handle.net/10353/d1021296
- Description: PMPSgLig-NaMMT nanocomposites were prepared from methacryloxypropyltrimethoxysilane (MPS), lignocellulose and montmorillonite clay. The potential enhancement of organic pollutant adsorption capabilities of PMPSgLig-NaMMT nanocomposite from water through functionalization was investigated. PMPSgLig-NaMMT was functionalized by esterification and etherification using different methods so as to increase the surface hydrophobicity of the material and hence improve its compatibility with the target pollutants. Specific chemical routes specially tailored for PMPSgLig-NaMMT were established for functionalization mostly based on the common esterification (Fischer esterification) and etherification (Williamson‟s etherification) reactions. In the functionalization methods, factors such as pH environment, nanocomposite composition, nature of functionalization moiety, and use of or absence of solvents and their variations were studied. FT-IR, XRD, SEM and TGA were used to characterize the synthesized and functionalized nanoadsorbents. The techniques showed successful functionalization via esterification and etherification methods albeit to different extents, with clear retention of the material‟s original structure though there were signs of degradation with some methods. Characterization was supported by adsorption studies to validate implications and draw conclusions. The use of 1,10-phenathroline as a model organic pollutant in water in the adsorption studies showed that adsorbents conformed to monolayer adsorption following pseudo-second order kinetics for adsorption of organic pollutants accurately represented. Most importantly the studies revealed the significant impact of the nanocomposite composition on the overall absorbent performance. Adsorption studies also showed that functionalization via esterification methods gave rise to better adsorbents.
- Full Text:
- Date Issued: 2015
- Authors: Mafukidze, Donovan M
- Date: 2015
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11356 , http://hdl.handle.net/10353/d1021296
- Description: PMPSgLig-NaMMT nanocomposites were prepared from methacryloxypropyltrimethoxysilane (MPS), lignocellulose and montmorillonite clay. The potential enhancement of organic pollutant adsorption capabilities of PMPSgLig-NaMMT nanocomposite from water through functionalization was investigated. PMPSgLig-NaMMT was functionalized by esterification and etherification using different methods so as to increase the surface hydrophobicity of the material and hence improve its compatibility with the target pollutants. Specific chemical routes specially tailored for PMPSgLig-NaMMT were established for functionalization mostly based on the common esterification (Fischer esterification) and etherification (Williamson‟s etherification) reactions. In the functionalization methods, factors such as pH environment, nanocomposite composition, nature of functionalization moiety, and use of or absence of solvents and their variations were studied. FT-IR, XRD, SEM and TGA were used to characterize the synthesized and functionalized nanoadsorbents. The techniques showed successful functionalization via esterification and etherification methods albeit to different extents, with clear retention of the material‟s original structure though there were signs of degradation with some methods. Characterization was supported by adsorption studies to validate implications and draw conclusions. The use of 1,10-phenathroline as a model organic pollutant in water in the adsorption studies showed that adsorbents conformed to monolayer adsorption following pseudo-second order kinetics for adsorption of organic pollutants accurately represented. Most importantly the studies revealed the significant impact of the nanocomposite composition on the overall absorbent performance. Adsorption studies also showed that functionalization via esterification methods gave rise to better adsorbents.
- Full Text:
- Date Issued: 2015
Biological evaluation and semi-synthesis of Isolated compounds from (Syzygium aromaticum (L.) Merr. & Perry) Buds
- Authors: Sibusiso, Rali
- Date: 2014
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11352 , http://hdl.handle.net/10353/d1021140
- Description: Natural products play a fundamental role in modern drug discovery as they continue providing diverse bioactive lead compounds for new drug formulation. However, isolation of these valued compounds is problematic. On the other hand, the morbidity and mortality rates caused by non-communicable diseases are increasing with improved longevity. Thus, the study herein focused on the isolation of plant-derived compounds from Syzygium aromaticum and evaluated their biological properties. Syzygium aromaticum is a well-known plant which belongs to family Myrtaceae. Dried flower buds of S. aromaticum were subjected to sequential solvent extraction. The ethyl acetate extract (15.535 g) was subjected to column chromatography using a silica gel (0.063-0.200 mm) for isolation. This has led to the isolation of three distinct compounds that were identified as eugenol, maslinic acid (MA) and oleanolic acid (OA). The structural elucidation of these valued compounds was done using NMR, GC-MS, LC-MS, FT-IR and Mp. Further semi-synthesis of the oleanolic acid afforded acetate and ester OA-derived compounds with better solubility properties. All these compounds were evaluated for analgesic and anti-inflammatory properties. All tested compounds were administered at a dose of 40 mg/kg to both Wistar rats and Swiss mice. Significant (p<0.01) analgesic and anti-inflammatory properties are obtained for all compounds. The effects of eugenol in all experiment were better except in the thermal-induced pain or tail flick test. In the case of modified compounds, the formalin induced pain test disclosed that oleanane derived compounds confessed analgesic and anti-inflammatory effects better than OA, whereas, in tale flick test oleanolic acid proved superior analgesic effects compared to all its derivatives with the exception of the acetyl-derivative. Acute anti-inflammatory test showed that acetyl-derivatives were more active than other compounds. In conclusion, chromatographic techniques and semi-synthesise of oleanolic acid have resulted to several plant-derived compounds with analgesic and anti-inflammatory properties. The semi-synthesized compounds may serve as alternative drug candidates for new analgesic and anti-inflammatory drug formulation
- Full Text:
- Date Issued: 2014
- Authors: Sibusiso, Rali
- Date: 2014
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11352 , http://hdl.handle.net/10353/d1021140
- Description: Natural products play a fundamental role in modern drug discovery as they continue providing diverse bioactive lead compounds for new drug formulation. However, isolation of these valued compounds is problematic. On the other hand, the morbidity and mortality rates caused by non-communicable diseases are increasing with improved longevity. Thus, the study herein focused on the isolation of plant-derived compounds from Syzygium aromaticum and evaluated their biological properties. Syzygium aromaticum is a well-known plant which belongs to family Myrtaceae. Dried flower buds of S. aromaticum were subjected to sequential solvent extraction. The ethyl acetate extract (15.535 g) was subjected to column chromatography using a silica gel (0.063-0.200 mm) for isolation. This has led to the isolation of three distinct compounds that were identified as eugenol, maslinic acid (MA) and oleanolic acid (OA). The structural elucidation of these valued compounds was done using NMR, GC-MS, LC-MS, FT-IR and Mp. Further semi-synthesis of the oleanolic acid afforded acetate and ester OA-derived compounds with better solubility properties. All these compounds were evaluated for analgesic and anti-inflammatory properties. All tested compounds were administered at a dose of 40 mg/kg to both Wistar rats and Swiss mice. Significant (p<0.01) analgesic and anti-inflammatory properties are obtained for all compounds. The effects of eugenol in all experiment were better except in the thermal-induced pain or tail flick test. In the case of modified compounds, the formalin induced pain test disclosed that oleanane derived compounds confessed analgesic and anti-inflammatory effects better than OA, whereas, in tale flick test oleanolic acid proved superior analgesic effects compared to all its derivatives with the exception of the acetyl-derivative. Acute anti-inflammatory test showed that acetyl-derivatives were more active than other compounds. In conclusion, chromatographic techniques and semi-synthesise of oleanolic acid have resulted to several plant-derived compounds with analgesic and anti-inflammatory properties. The semi-synthesized compounds may serve as alternative drug candidates for new analgesic and anti-inflammatory drug formulation
- Full Text:
- Date Issued: 2014
Development of a bench scale single batch biomass to liquid fuel facility
- Authors: Zhang, Yusheng
- Date: 2014
- Subjects: Biomass energy , Renewable energy sources , Energy conversion , Electric power production
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: http://hdl.handle.net/10353/811 , vital:26499 , Biomass energy , Renewable energy sources , Energy conversion , Electric power production
- Description: The research described in this dissertation was motivated by the global demand for energy that is not dependent on coal, oil, natural gas and other non-renewable fossil fuels. The technology used in this project is related to the use of biomass to produce a viable alternative to conventional sources of fuel. A bench scale biomass to liquid (BTL) facility was built and tested. This produced results confirming the feasibility of the BTL process. The findings of the pilot study outlined in this dissertation justified the conclusion that the next step will be to expand the capacity and productivity of the BTL pilot plant to an industrial scale. Biomass comes from a variety of renewable sources that are readily available. In this case, the material used in the fixed bed biomass gasification facility to generate wood gas was agricultural and forestry waste, such as straw and wood chips. The gasifier had the capacity to produce up to 10 cubic metres/hr of gas with a carbon monoxide and hydrogen content of between 20–40% by volume, when it was operated at ambient pressure and with air as the oxidizer. The gas, produced at a temperature above 700º C, was cooled in a quench/water scrubber in order to remove most of the mechanical impurities (tars and water-soluble inorganic particles), condensed and dried with corn cobs before being compressed in cylinders at over 100 bar (g) for use in the Fischer-Tropsch Synthesis (FTS). The syngas was subjected further to a series of refining processes which included removal of sulphur and oxygen. The sulphur removal technology chosen entailed applying modified activated carbon to adsorb H2S with the help of hydrolysis in order to convert organic sulphur impurities into H2S which reduced the sulphur content of the gas to less than 5 ppbv. Supported cobalt catalyst (100 grams), were loaded into a single-tube fixed bed FT reactor with an inner diameter of 50 mm. The reactor was fitted with a heating jacket through which, heated oil ran to cool the reactor during a normal reaction occurring at < 250 ºC, while nitrogen was used in the heating jacket during reduction, which occurred at temperatures up ~ 350 ºC. The FTS reaction was carried out at different pressures and temperatures. Liquid and wax products were produced from the facility. The properties of the liquid and solid hydrocarbons produced were found to be the same as FT products from other feed stocks, such as natural gas and coal.
- Full Text:
- Date Issued: 2014
- Authors: Zhang, Yusheng
- Date: 2014
- Subjects: Biomass energy , Renewable energy sources , Energy conversion , Electric power production
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: http://hdl.handle.net/10353/811 , vital:26499 , Biomass energy , Renewable energy sources , Energy conversion , Electric power production
- Description: The research described in this dissertation was motivated by the global demand for energy that is not dependent on coal, oil, natural gas and other non-renewable fossil fuels. The technology used in this project is related to the use of biomass to produce a viable alternative to conventional sources of fuel. A bench scale biomass to liquid (BTL) facility was built and tested. This produced results confirming the feasibility of the BTL process. The findings of the pilot study outlined in this dissertation justified the conclusion that the next step will be to expand the capacity and productivity of the BTL pilot plant to an industrial scale. Biomass comes from a variety of renewable sources that are readily available. In this case, the material used in the fixed bed biomass gasification facility to generate wood gas was agricultural and forestry waste, such as straw and wood chips. The gasifier had the capacity to produce up to 10 cubic metres/hr of gas with a carbon monoxide and hydrogen content of between 20–40% by volume, when it was operated at ambient pressure and with air as the oxidizer. The gas, produced at a temperature above 700º C, was cooled in a quench/water scrubber in order to remove most of the mechanical impurities (tars and water-soluble inorganic particles), condensed and dried with corn cobs before being compressed in cylinders at over 100 bar (g) for use in the Fischer-Tropsch Synthesis (FTS). The syngas was subjected further to a series of refining processes which included removal of sulphur and oxygen. The sulphur removal technology chosen entailed applying modified activated carbon to adsorb H2S with the help of hydrolysis in order to convert organic sulphur impurities into H2S which reduced the sulphur content of the gas to less than 5 ppbv. Supported cobalt catalyst (100 grams), were loaded into a single-tube fixed bed FT reactor with an inner diameter of 50 mm. The reactor was fitted with a heating jacket through which, heated oil ran to cool the reactor during a normal reaction occurring at < 250 ºC, while nitrogen was used in the heating jacket during reduction, which occurred at temperatures up ~ 350 ºC. The FTS reaction was carried out at different pressures and temperatures. Liquid and wax products were produced from the facility. The properties of the liquid and solid hydrocarbons produced were found to be the same as FT products from other feed stocks, such as natural gas and coal.
- Full Text:
- Date Issued: 2014
Ethanol production from lignocellulosic sugarcane leaves and tops
- Authors: Dodo, Charlie Marembu
- Date: 2014
- Subjects: Biomass energy , Ethanol as fuel , Lignocellulose
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11347 , http://hdl.handle.net/10353/d1019839 , Biomass energy , Ethanol as fuel , Lignocellulose
- Description: Various methods for the production of bioethanol using different feedstocks have been researched on. In most work on bioethanol synthesis from sugar cane, tops and leaves have been regarded as waste and generally removed and thrown away. In this work, lignocellulosic sugarcane leaves and tops were not discarded but instead used as biomass to evaluate their hydrolyzate content. The leaves and tops were hydrolysed using different methods, namely concentrated acid, dilute acid pre-treatment with subsequent enzyme hydrolysis and compared with a combination of oxidative alkali pretreatment and enzyme hydrolysis. Subsequent fermentation of the hydrolyzates into bioethanol was done using the yeast saccharomyces cerevisae. Acid hydrolysis has the problem of producing inhibitors, which have to be removed and this was done using overliming with calcium hydroxide and compared to sodium hydroxide neutralization. Oxidative alkali pre-treatment with enzyme hydrolysis gave the highest yields of fermentable sugars of 38% (g/g) using 7% (v/v) peroxide pre-treated biomass than 36% (g/g) for 5% (v/v) with the least inhibitors. Concentrated and dilute acid hydrolysis each gave yields of25% (g/g) and 22% (g/g) yields respectively although for acid a neutralization step was necessary and resulted in dilution. Alkaline neutralization of acid hydrolyzates using sodium hydroxide resulted in less dilution and loss of fermentable sugars as compared to overliming. Higher yields of bioethanol, 13.7 (g/l) were obtained from enzyme hydrolyzates than 6.9 (g/l) bioethanol from dilute acid hydrolyzates. There was more bioethanol yield 13.7 (g/l) after 72h of fermentation with the yeast than 7.0 (g/l) bioethanol after 24h. However, the longer fermentation period diminishes the value of the increase in yield by lowering the efficiency of the process.
- Full Text:
- Date Issued: 2014
- Authors: Dodo, Charlie Marembu
- Date: 2014
- Subjects: Biomass energy , Ethanol as fuel , Lignocellulose
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11347 , http://hdl.handle.net/10353/d1019839 , Biomass energy , Ethanol as fuel , Lignocellulose
- Description: Various methods for the production of bioethanol using different feedstocks have been researched on. In most work on bioethanol synthesis from sugar cane, tops and leaves have been regarded as waste and generally removed and thrown away. In this work, lignocellulosic sugarcane leaves and tops were not discarded but instead used as biomass to evaluate their hydrolyzate content. The leaves and tops were hydrolysed using different methods, namely concentrated acid, dilute acid pre-treatment with subsequent enzyme hydrolysis and compared with a combination of oxidative alkali pretreatment and enzyme hydrolysis. Subsequent fermentation of the hydrolyzates into bioethanol was done using the yeast saccharomyces cerevisae. Acid hydrolysis has the problem of producing inhibitors, which have to be removed and this was done using overliming with calcium hydroxide and compared to sodium hydroxide neutralization. Oxidative alkali pre-treatment with enzyme hydrolysis gave the highest yields of fermentable sugars of 38% (g/g) using 7% (v/v) peroxide pre-treated biomass than 36% (g/g) for 5% (v/v) with the least inhibitors. Concentrated and dilute acid hydrolysis each gave yields of25% (g/g) and 22% (g/g) yields respectively although for acid a neutralization step was necessary and resulted in dilution. Alkaline neutralization of acid hydrolyzates using sodium hydroxide resulted in less dilution and loss of fermentable sugars as compared to overliming. Higher yields of bioethanol, 13.7 (g/l) were obtained from enzyme hydrolyzates than 6.9 (g/l) bioethanol from dilute acid hydrolyzates. There was more bioethanol yield 13.7 (g/l) after 72h of fermentation with the yeast than 7.0 (g/l) bioethanol after 24h. However, the longer fermentation period diminishes the value of the increase in yield by lowering the efficiency of the process.
- Full Text:
- Date Issued: 2014
Isolation, Characterisation, and biological activity evaluation of essential Oils of Cymbopogon validus (Stapf) Stapf ex Burtt Davy and Hyparrhenia hirta (L.) Stapf
- Authors: Rungqu, Pamela
- Date: 2014
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11354 , http://hdl.handle.net/10353/d1021283
- Description: Cymbopogon validus and Hyparrhenia hirta belong to the Poaceae botanical family. Both plants are used as thatching material; H. hirta is also used for weaving mats and baskets. In this study, we investigated the anti-inflammatory effects of C. validus and H. hirta essential oils on fresh egg-albumin induced edema on Wistar rats. To fully understand the chemically induced anti-inflammatory properties of these plants, we first analyzed the chemical composition of the essential oils. The essential oils were analyzed using gas chromatography-mass spectrometry (GC-MS). In C. validus, 13 compounds accounted for 74.3% of fresh leaves oil, 14 compounds 71.8% of dried leaves oil and 12 compounds 73.3% of flower oil were identified from the GC-MS Chromatogram. The percentage yields were as follows fresh leaves oil 2.2%, dried leaves oil 2.0% and flower oil 2.4% v/w respectively. Linalool (3.2-29.6%) and northujane (4.4-16.9%) were the dominant compounds found in the 3 oils analyzed. While, α-terpineol 37.5% and verbenone 13.5% was only found in the fresh leaf oil, this was absent in the dried leaves oil and the flowers oil of C. validus. In H. hirta, 25 compounds accounted for 68.1% of fresh leaves oil, 40 compounds 71.9% of dried leaves oil, 23 compounds 77.6% of fresh flowers oil and 18 compounds 80.1% of dried flowers oil were identified from the GC-MS Chromatogram. The percentage yields obtained from the different parts were 3.4% for fresh leaves oil, 2.8% for dried leaves oil, 2.8% for fresh flowers oil and 0.7% for dried flowers oil v/w respectively. Northujane (8.5-30.0%), diisooctyl phthalate (4.4-26.5%), phytone (1.1-10.4%) were the dominant compounds found in the 4 oils analyzed. While, dibutyl phthalate 26.9% was only found in the fresh flowers and was absent in the dried flowers oil. Moreover, caryophyllene oxide (1.7-9.6%) was found in fresh leaves and dried flowers oil of H. hirta. In vivo analysis revealed that the two essential oils displayed significant edema inhibition effect overtime. They displayed strong anti-inflammatory properties when compared to control group. However, the H. hirta essential oil was more effective than that of C. validus. Linalool, α-terpineol, and northujane extracted from C. validus and H. hirta essential oils might have contributed to the anti-inflammatory effects observed in Wistar rats. This study, confirms the anti-inflammatory properties of C. validus and H. hirta suggesting that they may be used in diseases related to anti-inflammation.
- Full Text:
- Date Issued: 2014
- Authors: Rungqu, Pamela
- Date: 2014
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11354 , http://hdl.handle.net/10353/d1021283
- Description: Cymbopogon validus and Hyparrhenia hirta belong to the Poaceae botanical family. Both plants are used as thatching material; H. hirta is also used for weaving mats and baskets. In this study, we investigated the anti-inflammatory effects of C. validus and H. hirta essential oils on fresh egg-albumin induced edema on Wistar rats. To fully understand the chemically induced anti-inflammatory properties of these plants, we first analyzed the chemical composition of the essential oils. The essential oils were analyzed using gas chromatography-mass spectrometry (GC-MS). In C. validus, 13 compounds accounted for 74.3% of fresh leaves oil, 14 compounds 71.8% of dried leaves oil and 12 compounds 73.3% of flower oil were identified from the GC-MS Chromatogram. The percentage yields were as follows fresh leaves oil 2.2%, dried leaves oil 2.0% and flower oil 2.4% v/w respectively. Linalool (3.2-29.6%) and northujane (4.4-16.9%) were the dominant compounds found in the 3 oils analyzed. While, α-terpineol 37.5% and verbenone 13.5% was only found in the fresh leaf oil, this was absent in the dried leaves oil and the flowers oil of C. validus. In H. hirta, 25 compounds accounted for 68.1% of fresh leaves oil, 40 compounds 71.9% of dried leaves oil, 23 compounds 77.6% of fresh flowers oil and 18 compounds 80.1% of dried flowers oil were identified from the GC-MS Chromatogram. The percentage yields obtained from the different parts were 3.4% for fresh leaves oil, 2.8% for dried leaves oil, 2.8% for fresh flowers oil and 0.7% for dried flowers oil v/w respectively. Northujane (8.5-30.0%), diisooctyl phthalate (4.4-26.5%), phytone (1.1-10.4%) were the dominant compounds found in the 4 oils analyzed. While, dibutyl phthalate 26.9% was only found in the fresh flowers and was absent in the dried flowers oil. Moreover, caryophyllene oxide (1.7-9.6%) was found in fresh leaves and dried flowers oil of H. hirta. In vivo analysis revealed that the two essential oils displayed significant edema inhibition effect overtime. They displayed strong anti-inflammatory properties when compared to control group. However, the H. hirta essential oil was more effective than that of C. validus. Linalool, α-terpineol, and northujane extracted from C. validus and H. hirta essential oils might have contributed to the anti-inflammatory effects observed in Wistar rats. This study, confirms the anti-inflammatory properties of C. validus and H. hirta suggesting that they may be used in diseases related to anti-inflammation.
- Full Text:
- Date Issued: 2014
Preparation and characterisation of nanocomposites of biomass and montmorillonite clay for use as biofuels
- Authors: Nyamutswa, Lavern Tendayi
- Date: 2014
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11345 , http://hdl.handle.net/10353/d1019779
- Description: The aim of the study was to prepare composites of clay and biomass which burn longer than unmodified biomass. Montmorillonite clay was converted to mono-ionic clay by ion exchange with sodium using sodium chloride solution. The mono-ionic clay was organically modified with an organic surfactant, methyl triphenyl phosphonium bromide. Nanocomposites were then prepared by combining the modified forms of the clay with sawdust. The three forms of clay used for the formation of composites were unmodified montmorillonite, mono-ionic montmorillonite and organically modified montmorillonite. The solution blending method was used to make the nanocomposites. FT-IR and XRD analysis showed that organic surfactant increases the interlayer space of the clay since it is bulkier than the inorganic cations that are naturally present in the interlayer space of montmorillonite. The combination of clay and sawdust resulted in the formation of exfoliated nanocomposites as shown by the absence of peaks in the low 2 theta angle in the x-ray diffraction data of the nanocomposite. The nanocomposite which was made from sawdust and 1% organically modified clay showed the best results in terms of burning time and thermal stability, as well as giving a calorific value closest to unmodified sawdust and the least amount of residue.
- Full Text:
- Date Issued: 2014
- Authors: Nyamutswa, Lavern Tendayi
- Date: 2014
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11345 , http://hdl.handle.net/10353/d1019779
- Description: The aim of the study was to prepare composites of clay and biomass which burn longer than unmodified biomass. Montmorillonite clay was converted to mono-ionic clay by ion exchange with sodium using sodium chloride solution. The mono-ionic clay was organically modified with an organic surfactant, methyl triphenyl phosphonium bromide. Nanocomposites were then prepared by combining the modified forms of the clay with sawdust. The three forms of clay used for the formation of composites were unmodified montmorillonite, mono-ionic montmorillonite and organically modified montmorillonite. The solution blending method was used to make the nanocomposites. FT-IR and XRD analysis showed that organic surfactant increases the interlayer space of the clay since it is bulkier than the inorganic cations that are naturally present in the interlayer space of montmorillonite. The combination of clay and sawdust resulted in the formation of exfoliated nanocomposites as shown by the absence of peaks in the low 2 theta angle in the x-ray diffraction data of the nanocomposite. The nanocomposite which was made from sawdust and 1% organically modified clay showed the best results in terms of burning time and thermal stability, as well as giving a calorific value closest to unmodified sawdust and the least amount of residue.
- Full Text:
- Date Issued: 2014
Gasification characteristics of sugarcane bagasse
- Authors: Anukam, Anthony Ike
- Date: 2013
- Subjects: Bagasse -- Bagasse industry , Sugarcane -- Biotechnology , Computer simulation
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11343 , http://hdl.handle.net/10353/d1016170 , Bagasse -- Bagasse industry , Sugarcane -- Biotechnology , Computer simulation
- Description: Sugarcane is a major crop in many countries. It is the most abundant lignocellulosic material in tropical countries such as South Africa. It is one of the plants with the highest bioconversion efficiency. The sugarcane crop is able to efficiently fix solar energy, yielding some 55 tons of dry matter per hectare of land annually. After harvest, the crop produces sugar juice and bagasse. Sugarcane bagasse is a residue that results from the crushing of sugarcane in the sugar industry. It is a renewable feedstock that can be used for power generation and manufacturing cellulosic ethanol. As biomass, sugarcane bagasse holds promise as a fuel source since it can produce more than enough electricity and heat energy to supply the needs of a common sugar factory. However, in the sugarcane industry the bagasse is currently burnt inefficiently in boilers that provide the heating for the industry. This project seeks to investigate the possibility of gasifying sugarcane bagasse as an efficient conversion technology. The investigation is necessary because fuel properties govern the gasifier design and ultimately, the gasification efficiency. Proximate and ultimate analysis of sugarcane bagasse was conducted after which the results were used to conduct a computer simulation of the mass and energy balance during gasification. The kinetic investigation undertaken through the TGA and DTG analyses revealed the activation energy and pre – exponential factor which were obtained by the model – free Kissinger method of kinetic analysis and were found to be 181.51 kJ/mol and 3.1 × 103/min respectively. The heating value of sugarcane bagasse was also measured and found to be 17.8 MJ/kg, which was used in the calculation of the conversion efficiency of the gasification process. Fuel properties, including moisture content and gasifier operating parameters were varied in order to determine optimum gasifier operating conditions that results in maximum conversion efficiency. The highest conversion efficiency was achieved at low moisture content after computer simulation of the gasification process. Moisture content also affected the volume of CO and H2 as the former decreases with increasing moisture content while the latter increases with increasing moisture content, accelerating the water – gas reaction. Scanning electron microscope fitted to an Energy dispersive X – ray spectroscopy was also used in order to view the shape and size distribution as well as determine the elemental composition of sugarcane bagasse. The results obtained established that the fuel properties and gasification conditions affect the conversion efficiency. During computer simulation, it was established that smaller particle size resulted in higher conversion efficiency. The smaller throat diameter also resulted in higher conversion efficiency. The throat angle of 25° also resulted in higher conversion efficiency. The temperature of input air was also found to be one of the major determining factors in terms of conversion efficiency. The dissertation presents the proximate and ultimate analysis results as well as the kinetic analysis results. The SEM/EDX analysis as well as the computer simulation results of the gasification process is also presented. The major contribution of this project was on the investigation of the gasification characteristics of sugarcane bagasse and the utilization of these in the design of a laboratory scale sugarcane bagasse gasifier with enhanced conversion efficiency through computer simulation.
- Full Text:
- Date Issued: 2013
- Authors: Anukam, Anthony Ike
- Date: 2013
- Subjects: Bagasse -- Bagasse industry , Sugarcane -- Biotechnology , Computer simulation
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11343 , http://hdl.handle.net/10353/d1016170 , Bagasse -- Bagasse industry , Sugarcane -- Biotechnology , Computer simulation
- Description: Sugarcane is a major crop in many countries. It is the most abundant lignocellulosic material in tropical countries such as South Africa. It is one of the plants with the highest bioconversion efficiency. The sugarcane crop is able to efficiently fix solar energy, yielding some 55 tons of dry matter per hectare of land annually. After harvest, the crop produces sugar juice and bagasse. Sugarcane bagasse is a residue that results from the crushing of sugarcane in the sugar industry. It is a renewable feedstock that can be used for power generation and manufacturing cellulosic ethanol. As biomass, sugarcane bagasse holds promise as a fuel source since it can produce more than enough electricity and heat energy to supply the needs of a common sugar factory. However, in the sugarcane industry the bagasse is currently burnt inefficiently in boilers that provide the heating for the industry. This project seeks to investigate the possibility of gasifying sugarcane bagasse as an efficient conversion technology. The investigation is necessary because fuel properties govern the gasifier design and ultimately, the gasification efficiency. Proximate and ultimate analysis of sugarcane bagasse was conducted after which the results were used to conduct a computer simulation of the mass and energy balance during gasification. The kinetic investigation undertaken through the TGA and DTG analyses revealed the activation energy and pre – exponential factor which were obtained by the model – free Kissinger method of kinetic analysis and were found to be 181.51 kJ/mol and 3.1 × 103/min respectively. The heating value of sugarcane bagasse was also measured and found to be 17.8 MJ/kg, which was used in the calculation of the conversion efficiency of the gasification process. Fuel properties, including moisture content and gasifier operating parameters were varied in order to determine optimum gasifier operating conditions that results in maximum conversion efficiency. The highest conversion efficiency was achieved at low moisture content after computer simulation of the gasification process. Moisture content also affected the volume of CO and H2 as the former decreases with increasing moisture content while the latter increases with increasing moisture content, accelerating the water – gas reaction. Scanning electron microscope fitted to an Energy dispersive X – ray spectroscopy was also used in order to view the shape and size distribution as well as determine the elemental composition of sugarcane bagasse. The results obtained established that the fuel properties and gasification conditions affect the conversion efficiency. During computer simulation, it was established that smaller particle size resulted in higher conversion efficiency. The smaller throat diameter also resulted in higher conversion efficiency. The throat angle of 25° also resulted in higher conversion efficiency. The temperature of input air was also found to be one of the major determining factors in terms of conversion efficiency. The dissertation presents the proximate and ultimate analysis results as well as the kinetic analysis results. The SEM/EDX analysis as well as the computer simulation results of the gasification process is also presented. The major contribution of this project was on the investigation of the gasification characteristics of sugarcane bagasse and the utilization of these in the design of a laboratory scale sugarcane bagasse gasifier with enhanced conversion efficiency through computer simulation.
- Full Text:
- Date Issued: 2013
Phytochemical analyses and Brine shrimp (Artemia Salina) lethality studies on Syzygium cordatum
- Authors: Chiguvare, Herbert
- Date: 2013
- Subjects: Artemia , Crustacea , Chromatographic analysis , Medicinal plants , Essences and essential oils , Traditional medicine
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11336 , http://hdl.handle.net/10353/d1004352 , Artemia , Crustacea , Chromatographic analysis , Medicinal plants , Essences and essential oils , Traditional medicine
- Description: Syzygium cordatum Hoscht ex. C Krauss, also known as water berry, is normally used by the people of South Africa for respiratory ailments including tuberculosis, stomach complaints, treatment of wounds and as emetics. An extract of the leaves can be used as a purgative for diarrhoea treatment. The leaves of Syzygium cordatum Myrtaceae were obtained from the Eastern Cape Province of South Africa, air dried and sequential solvent extraction was done to obtain various non volatile crude extracts. The volatile extract, that is the essential oil was extracted from the leaves using hydrodistillation and analysis of compounds was done by GC/MS for composition. 32 compounds were obtained from the fresh leaves and 18 compounds were obtained from the dry leaves. The fresh oil contains caryophyllene (11.8 percent) and caryophyllene oxide (11.1 percent) as the main sesquiterpene component. α-Pinene(5.0 percent) was the only monoterpene compound identified in the fresh oil in substantial amount. The dry leaves oil had copanene (17.0 percent), β-Caryophellene (26.0 percent), cubenol (6.5 percent) and caryophellene oxide (14.2 percent) as the dominant constituent of the oil. Summary of the classes of compounds in the oil revealed that the chemical profile of both oils were dominated by sesquiterpenoid compounds. This is the first time that terpenoids compounds are being identified in both the fresh and dry leaf oil of S. cordatum. Hexane leaf extract was selected due to the interest in the terpenoid compounds. Column chromatography of the hexane crude gave five (5) of which two are fully reported. The isolates were fully elucidated using spectroscopic methods to be β-Sitosterol (HC3) and Friedela-3-one (HC1A/HC1D). Cytotoxicity analysis was carried out on the crude using the Brine shrimps assay. Isolates 1C and1D showed significant lethality using the brine shrimps assay with lethality values (LC50) of 4.105mg/ml for HC1C and 4.11mg/ml for 1D/1A respectively.
- Full Text:
- Date Issued: 2013
- Authors: Chiguvare, Herbert
- Date: 2013
- Subjects: Artemia , Crustacea , Chromatographic analysis , Medicinal plants , Essences and essential oils , Traditional medicine
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11336 , http://hdl.handle.net/10353/d1004352 , Artemia , Crustacea , Chromatographic analysis , Medicinal plants , Essences and essential oils , Traditional medicine
- Description: Syzygium cordatum Hoscht ex. C Krauss, also known as water berry, is normally used by the people of South Africa for respiratory ailments including tuberculosis, stomach complaints, treatment of wounds and as emetics. An extract of the leaves can be used as a purgative for diarrhoea treatment. The leaves of Syzygium cordatum Myrtaceae were obtained from the Eastern Cape Province of South Africa, air dried and sequential solvent extraction was done to obtain various non volatile crude extracts. The volatile extract, that is the essential oil was extracted from the leaves using hydrodistillation and analysis of compounds was done by GC/MS for composition. 32 compounds were obtained from the fresh leaves and 18 compounds were obtained from the dry leaves. The fresh oil contains caryophyllene (11.8 percent) and caryophyllene oxide (11.1 percent) as the main sesquiterpene component. α-Pinene(5.0 percent) was the only monoterpene compound identified in the fresh oil in substantial amount. The dry leaves oil had copanene (17.0 percent), β-Caryophellene (26.0 percent), cubenol (6.5 percent) and caryophellene oxide (14.2 percent) as the dominant constituent of the oil. Summary of the classes of compounds in the oil revealed that the chemical profile of both oils were dominated by sesquiterpenoid compounds. This is the first time that terpenoids compounds are being identified in both the fresh and dry leaf oil of S. cordatum. Hexane leaf extract was selected due to the interest in the terpenoid compounds. Column chromatography of the hexane crude gave five (5) of which two are fully reported. The isolates were fully elucidated using spectroscopic methods to be β-Sitosterol (HC3) and Friedela-3-one (HC1A/HC1D). Cytotoxicity analysis was carried out on the crude using the Brine shrimps assay. Isolates 1C and1D showed significant lethality using the brine shrimps assay with lethality values (LC50) of 4.105mg/ml for HC1C and 4.11mg/ml for 1D/1A respectively.
- Full Text:
- Date Issued: 2013
Synthesis and characterization of metal sulfide nanoparticles/polymer nanocomposites
- Authors: Mbese, Johannes Zanoxolo
- Date: 2013
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11344 , http://hdl.handle.net/10353/d1016190
- Description: The focus of this project was to synthesize and characterize metal sulfide nanoparticles /polymer nanocomposites. The work involved the synthesis of dithiocarbamato ligands and complexes derived from aniline. Zn(II), Cd(II) and Hg(II) dithiocarbamato complexes were used as single-molecule precursors for the synthesis of the ZnS, CdS and HgS nanoparticles and their optical and structural properties studied. The other focus of this work was to synthesize a combined functionality metal sulfide nanoparticles/polymer nanocomposites by dispersing as-synthesized ZnS, CdS and HgS nanoparticles in polymethyl methacrylate (PMMA) matrix. The characterization of the ligands, complexes, nanoparticles and nanocomposites were investigated using relevant instrumental tools like UV-Vis, photoluminescence (PL), Fourier transform infrared (FTIR), X-ray diffraction (XRD), energy dispersion X-ray (EDX), nuclear magnetic resonance (NMR), scanning electron microscopy (SEM) and transmission electron microscopy (TEM).
- Full Text:
- Date Issued: 2013
- Authors: Mbese, Johannes Zanoxolo
- Date: 2013
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11344 , http://hdl.handle.net/10353/d1016190
- Description: The focus of this project was to synthesize and characterize metal sulfide nanoparticles /polymer nanocomposites. The work involved the synthesis of dithiocarbamato ligands and complexes derived from aniline. Zn(II), Cd(II) and Hg(II) dithiocarbamato complexes were used as single-molecule precursors for the synthesis of the ZnS, CdS and HgS nanoparticles and their optical and structural properties studied. The other focus of this work was to synthesize a combined functionality metal sulfide nanoparticles/polymer nanocomposites by dispersing as-synthesized ZnS, CdS and HgS nanoparticles in polymethyl methacrylate (PMMA) matrix. The characterization of the ligands, complexes, nanoparticles and nanocomposites were investigated using relevant instrumental tools like UV-Vis, photoluminescence (PL), Fourier transform infrared (FTIR), X-ray diffraction (XRD), energy dispersion X-ray (EDX), nuclear magnetic resonance (NMR), scanning electron microscopy (SEM) and transmission electron microscopy (TEM).
- Full Text:
- Date Issued: 2013
The characterization and electrochemistry of dye-sensitized solar cells
- Authors: Caga, Noloyiso
- Date: 2013
- Subjects: Dye-sensitized solar cells , Acetonitrile , Electrochemistry , Spectrum analysis
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11341 , http://hdl.handle.net/10353/d1016069 , Dye-sensitized solar cells , Acetonitrile , Electrochemistry , Spectrum analysis
- Description: In this study a presentation of the technology behind dye-sensitized solar cells, their design as well as the role of the different parts of the cell. The characterization of the cell is divided into four sections namely: the characterization of the paste required to make the TiO2 film and its optical properties using SEM-EDX and XRD analytical techniques; Analysis of the various absorptions of three Ru-based dyes using UV-Vis spectroscopy, Photoluminescence and Fourier Transform Infra-Red spectroscopy; the characterization and the analyses of the entire cell using Electrochemical Impedance Spectroscopy. The nine cells were prepared by examining RuL2(CN)2 , RuL2(NCS)2 or N3 dye and RuL2(NCS)2 TBA+ or N719 dye. [L = 2,2'-bipyridyl-4,4'-dicarboxylic acid ;TBA = tetra-butyl ammonium] were combined with three electrolytes namely: Z–150 , AN–50 and PN–50. The Iodolyte PN–50 is an iodide based low viscosity electrolyte with 50 mM of tri-iodide dissolved in a solvent called propionitrile (PN). The Iodolyte AN–50 is an iodide based low viscosity electrolyte with 50 mM of tri-iodide dissolved in a solvent called acetonitrile (AN). The Iodolyte Z–150 is an iodide based low viscosity electrolyte with 150 mM of tri-iodide dissolved in a solvent called 3-methoxypropionitrile (MPN) and with additives such an ionic liquid, malkylbenziimidazole and guanidine thiocyanate. A solar simulator was utilized with which the standard solar irradiation can be created in laboratory conditions. The fill factors as well as overall performance efficiencies of the these cells are quite low < 1.0%,.
- Full Text:
- Date Issued: 2013
- Authors: Caga, Noloyiso
- Date: 2013
- Subjects: Dye-sensitized solar cells , Acetonitrile , Electrochemistry , Spectrum analysis
- Language: English
- Type: Thesis , Masters , MSc (Chemistry)
- Identifier: vital:11341 , http://hdl.handle.net/10353/d1016069 , Dye-sensitized solar cells , Acetonitrile , Electrochemistry , Spectrum analysis
- Description: In this study a presentation of the technology behind dye-sensitized solar cells, their design as well as the role of the different parts of the cell. The characterization of the cell is divided into four sections namely: the characterization of the paste required to make the TiO2 film and its optical properties using SEM-EDX and XRD analytical techniques; Analysis of the various absorptions of three Ru-based dyes using UV-Vis spectroscopy, Photoluminescence and Fourier Transform Infra-Red spectroscopy; the characterization and the analyses of the entire cell using Electrochemical Impedance Spectroscopy. The nine cells were prepared by examining RuL2(CN)2 , RuL2(NCS)2 or N3 dye and RuL2(NCS)2 TBA+ or N719 dye. [L = 2,2'-bipyridyl-4,4'-dicarboxylic acid ;TBA = tetra-butyl ammonium] were combined with three electrolytes namely: Z–150 , AN–50 and PN–50. The Iodolyte PN–50 is an iodide based low viscosity electrolyte with 50 mM of tri-iodide dissolved in a solvent called propionitrile (PN). The Iodolyte AN–50 is an iodide based low viscosity electrolyte with 50 mM of tri-iodide dissolved in a solvent called acetonitrile (AN). The Iodolyte Z–150 is an iodide based low viscosity electrolyte with 150 mM of tri-iodide dissolved in a solvent called 3-methoxypropionitrile (MPN) and with additives such an ionic liquid, malkylbenziimidazole and guanidine thiocyanate. A solar simulator was utilized with which the standard solar irradiation can be created in laboratory conditions. The fill factors as well as overall performance efficiencies of the these cells are quite low < 1.0%,.
- Full Text:
- Date Issued: 2013
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