Phthalocyanine-nanoparticle conjugates supported on inorganic nanofibers as photocatalysts for the treatment of biological and organic pollutants as well as for hydrogen generation
- Authors: Mapukata, Sivuyisiwe
- Date: 2021-10-29
- Subjects: Phthalocyanines , Nanofibers , Nanoparticles , Zinc , Hydrogen , Organic water pollutants , Water Purification , Electrospinning , Photocatalysis , Photodegradation , Anti-infective agents
- Language: English
- Type: Doctoral theses , text
- Identifier: http://hdl.handle.net/10962/192831 , vital:45268 , 10.21504/10962/192831
- Description: This thesis reports on the synthesis, photophysicochemical and photocatalytic properties of various zinc phthalocyanines (Pcs). For enhanced properties and catalyst support, the reported Pcs were conjugated to different nanoparticles (NPs) through chemisorption as well as amide bond formation to yield Pc-NP conjugates. For increased catalyst surface area and catalyst reusability, the Pcs and some of their conjugates were also supported on electrospun inorganic nanofibers i.e. SiO2, hematite (abbreviated Hem and has formula α-Fe2O3), ZnO and TiO2 nanofibers. The effect that the number of charges on a Pc has on its antimicrobial activities was evaluated by comparing the photoactivities of neutral, octacationic and hexadecacationic Pcs against S. aureus, E. coli and C. albicans. The extent of enhancement of their antimicrobial activities upon conjugation (through chemisorption) to Ag NPs was also studied in solution and when supported on SiO2 nanofibers. The results showed that the hexadecacationic complex 3 possessed the best antimicrobial activity against all three microorganisms, in solution and when supported on the SiO2 nanofibers. Covalent conjugation of Pcs with carboxylic acid moieties (complexes 4-6) to amine functionalised NPs (Cys-Ag, NH2-Fe3O4 and Cys-Fe3O4@Ag) resulted in enhanced singlet oxygen generation and thus antibacterial efficiencies. Comparison of the photodegradation efficiencies of semiconductor nanofibers (hematite, ZnO and TiO2) when bare and when modified with a Pc (complex 6) were evaluated. Modification of the nanofibers with the Pc resulted in enhanced photoactivities for the nanofibers with the hematite nanofibers being the best. Modification of the hematite nanofibers with two different Pcs i.e. monosubstituted (complex 5) and an asymmetrical tetrasubstituted Pc (complex 6) showed that complex 6 better enhanced the activity of the nanofibers. Evaluation of the hydrogen generation efficiencies of the bare and modified TiO2 nanofibers calcined at different temperatures demonstrated that the anatase nanofibers calcined at 500 oC possessed the best catalytic efficiency. The efficiency of the TiO2 nanofibers was enhanced in the presence of the Co and Pd NPs as well as a Pc (complex 7), with the extent of enhancement being the greatest for the nanofibers modified with the Pd NPs. The reported findings therefore demonstrate the versatility of applications of Pcs for different water purification techniques when supported on different nanomaterials. , Thesis (PhD) -- Faculty of Science, Chemistry, 2021
- Full Text:
- Date Issued: 2021-10-29
- Authors: Mapukata, Sivuyisiwe
- Date: 2021-10-29
- Subjects: Phthalocyanines , Nanofibers , Nanoparticles , Zinc , Hydrogen , Organic water pollutants , Water Purification , Electrospinning , Photocatalysis , Photodegradation , Anti-infective agents
- Language: English
- Type: Doctoral theses , text
- Identifier: http://hdl.handle.net/10962/192831 , vital:45268 , 10.21504/10962/192831
- Description: This thesis reports on the synthesis, photophysicochemical and photocatalytic properties of various zinc phthalocyanines (Pcs). For enhanced properties and catalyst support, the reported Pcs were conjugated to different nanoparticles (NPs) through chemisorption as well as amide bond formation to yield Pc-NP conjugates. For increased catalyst surface area and catalyst reusability, the Pcs and some of their conjugates were also supported on electrospun inorganic nanofibers i.e. SiO2, hematite (abbreviated Hem and has formula α-Fe2O3), ZnO and TiO2 nanofibers. The effect that the number of charges on a Pc has on its antimicrobial activities was evaluated by comparing the photoactivities of neutral, octacationic and hexadecacationic Pcs against S. aureus, E. coli and C. albicans. The extent of enhancement of their antimicrobial activities upon conjugation (through chemisorption) to Ag NPs was also studied in solution and when supported on SiO2 nanofibers. The results showed that the hexadecacationic complex 3 possessed the best antimicrobial activity against all three microorganisms, in solution and when supported on the SiO2 nanofibers. Covalent conjugation of Pcs with carboxylic acid moieties (complexes 4-6) to amine functionalised NPs (Cys-Ag, NH2-Fe3O4 and Cys-Fe3O4@Ag) resulted in enhanced singlet oxygen generation and thus antibacterial efficiencies. Comparison of the photodegradation efficiencies of semiconductor nanofibers (hematite, ZnO and TiO2) when bare and when modified with a Pc (complex 6) were evaluated. Modification of the nanofibers with the Pc resulted in enhanced photoactivities for the nanofibers with the hematite nanofibers being the best. Modification of the hematite nanofibers with two different Pcs i.e. monosubstituted (complex 5) and an asymmetrical tetrasubstituted Pc (complex 6) showed that complex 6 better enhanced the activity of the nanofibers. Evaluation of the hydrogen generation efficiencies of the bare and modified TiO2 nanofibers calcined at different temperatures demonstrated that the anatase nanofibers calcined at 500 oC possessed the best catalytic efficiency. The efficiency of the TiO2 nanofibers was enhanced in the presence of the Co and Pd NPs as well as a Pc (complex 7), with the extent of enhancement being the greatest for the nanofibers modified with the Pd NPs. The reported findings therefore demonstrate the versatility of applications of Pcs for different water purification techniques when supported on different nanomaterials. , Thesis (PhD) -- Faculty of Science, Chemistry, 2021
- Full Text:
- Date Issued: 2021-10-29
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
Photocatalysis of 4-chloro and 4-nonylphenols using novel symmetric phthalocyanines and asymmetric porphyrin supported on polyacrylonitrite nanofibres
- Authors: Jones, Benjamin Martin
- Date: 2020
- Subjects: Nanoparticles , Phthalocyanines , Electrospinning , Porphyrins , Nanofibers , Photocatalysis , Photocatalysis -- Environmental aspects
- Language: English
- Type: text , Thesis , Masters , MSc
- Identifier: http://hdl.handle.net/10962/164770 , vital:41163
- Description: This work explores the synthesis and characterisation of novel symmetrical phthalocyanines and novel asymmetric porphyrins that have been embedded or linked respectively,and electrospun into fibres for application in the photocatalysis of environmental pollutants. The phthalocyanines contain pyrrole moieties without hetero atom linkers to maintain a rigid structure. The porphyrin contains a carboxy moiety utilized to construct an amide bond between the complex and the polymer prior to the spinning process. The new compounds were characterized by elemental analyses, proton nuclear magnetic resonance (HNMR)Fourier-transform infrared spectroscopy (FTIR), MALDI-TOF and UV-vis spectroscopy. The general trends of fluorescence, triplet and singlet oxygen quantum yields are described as well as their appropriate lifetimes. The photocatalytic activity of phthalocyanine embedded fibres were compared against those that had been dyed. Unfortunately, during the degradation process, the dyed fibres leeched compound and the studies could not be continued. It was seen that the porphyrin fibres linked to the polymer showed the most efficient photocatalytic activity against 4-cholorphenol and 4-nonylphenol due to irradiation at lower wavelengths consequently having higher frequencies and transferring more energy.
- Full Text:
- Date Issued: 2020
- Authors: Jones, Benjamin Martin
- Date: 2020
- Subjects: Nanoparticles , Phthalocyanines , Electrospinning , Porphyrins , Nanofibers , Photocatalysis , Photocatalysis -- Environmental aspects
- Language: English
- Type: text , Thesis , Masters , MSc
- Identifier: http://hdl.handle.net/10962/164770 , vital:41163
- Description: This work explores the synthesis and characterisation of novel symmetrical phthalocyanines and novel asymmetric porphyrins that have been embedded or linked respectively,and electrospun into fibres for application in the photocatalysis of environmental pollutants. The phthalocyanines contain pyrrole moieties without hetero atom linkers to maintain a rigid structure. The porphyrin contains a carboxy moiety utilized to construct an amide bond between the complex and the polymer prior to the spinning process. The new compounds were characterized by elemental analyses, proton nuclear magnetic resonance (HNMR)Fourier-transform infrared spectroscopy (FTIR), MALDI-TOF and UV-vis spectroscopy. The general trends of fluorescence, triplet and singlet oxygen quantum yields are described as well as their appropriate lifetimes. The photocatalytic activity of phthalocyanine embedded fibres were compared against those that had been dyed. Unfortunately, during the degradation process, the dyed fibres leeched compound and the studies could not be continued. It was seen that the porphyrin fibres linked to the polymer showed the most efficient photocatalytic activity against 4-cholorphenol and 4-nonylphenol due to irradiation at lower wavelengths consequently having higher frequencies and transferring more energy.
- 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
Phthalocyanine-nanoparticle conjugates for photodynamic therapy of cancer and phototransformation of organic pollutants
- Authors: Khoza, Phindile Brenda
- Date: 2015
- Subjects: Phthalocyanines , Nanoparticles , Photochemotherapy , Cancer -- Chemotherapy , Zinc oxide , Photocatalysis
- Language: English
- Type: Thesis , Doctoral , PhD
- Identifier: vital:4538 , http://hdl.handle.net/10962/d1017918
- Description: The synthesis and extensive spectroscopical characterization of novel phthalocyanines are reported. The new compounds were characterized by elemental analysis, FT-IR, ¹HNMR, mass spectrometry and UV–Vis spectroscopy. The new phthalocyanines showed remarkable photophysicochemical behaviour. The novel phthalocyanines were then conjugated to nanoparticles, silver and ZnO. The coupling of the novel Pcs to nanoparticles was through covalent bonding and ligand exchange. These conjugates were supported onto electrospun polystyrene fibers and chitosan microbeads for use as photocatalysts. The efficiency of the immobilized Pcs and Pc-nanoparticles was assessed by the phototrasfromation of organic pollutants, methyl orange and Rhodamine 6G as model dyes. Upon conjugating phthalocyanines to nanoparticles, there was a great increase in the rate of photodegradation of the model dyes. The photodynamic activity of the novel phthalocyanines upon conjugating to nanoparticles and selected targeting agents is also reported. The targeting agents employed in this study are folic acid and polylysine. Conjugating the phthalocyanines to folic acid or polylysine improved the solubility of the phthalocyanines in aqueous media. The potency of the conjugates was investigated on breast (MCF-7), prostate and melanoma cancer cell lines. The phthalocyanines showed no toxicity in the absence of light. However, upon illumination, a concentration dependent cellular decrease was observed.
- Full Text:
- Date Issued: 2015
- Authors: Khoza, Phindile Brenda
- Date: 2015
- Subjects: Phthalocyanines , Nanoparticles , Photochemotherapy , Cancer -- Chemotherapy , Zinc oxide , Photocatalysis
- Language: English
- Type: Thesis , Doctoral , PhD
- Identifier: vital:4538 , http://hdl.handle.net/10962/d1017918
- Description: The synthesis and extensive spectroscopical characterization of novel phthalocyanines are reported. The new compounds were characterized by elemental analysis, FT-IR, ¹HNMR, mass spectrometry and UV–Vis spectroscopy. The new phthalocyanines showed remarkable photophysicochemical behaviour. The novel phthalocyanines were then conjugated to nanoparticles, silver and ZnO. The coupling of the novel Pcs to nanoparticles was through covalent bonding and ligand exchange. These conjugates were supported onto electrospun polystyrene fibers and chitosan microbeads for use as photocatalysts. The efficiency of the immobilized Pcs and Pc-nanoparticles was assessed by the phototrasfromation of organic pollutants, methyl orange and Rhodamine 6G as model dyes. Upon conjugating phthalocyanines to nanoparticles, there was a great increase in the rate of photodegradation of the model dyes. The photodynamic activity of the novel phthalocyanines upon conjugating to nanoparticles and selected targeting agents is also reported. The targeting agents employed in this study are folic acid and polylysine. Conjugating the phthalocyanines to folic acid or polylysine improved the solubility of the phthalocyanines in aqueous media. The potency of the conjugates was investigated on breast (MCF-7), prostate and melanoma cancer cell lines. The phthalocyanines showed no toxicity in the absence of light. However, upon illumination, a concentration dependent cellular decrease was observed.
- Full Text:
- Date Issued: 2015
Characterization and application of phthalocyanine-gold nanoparticle conjugates
- Authors: Tombe, Sekai Lana
- Date: 2013
- Subjects: Phthalocyanines , Gold , Zinc , Nanoparticles , Bioconjugates , Photochemistry , Photocatalysis , Electrospinning , Polymers , Pollutants , Phenols , Azo dyes
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:4293 , http://hdl.handle.net/10962/d1004517 , Phthalocyanines , Gold , Zinc , Nanoparticles , Bioconjugates , Photochemistry , Photocatalysis , Electrospinning , Polymers , Pollutants , Phenols , Azo dyes
- Description: This work presents the syntheses, photophysical and photochemical characterization of arylthio zinc phthalocyanines and their gold nanoparticle conjugates. Spectroscopic and microscopic studies confirmed the formation of the phthalocyanine-gold nanoparticle conjugates which exhibited enhanced photophysicochemical properties in comparison to the phthalocyanines. The studies showed that the presence of gold nanoparticles significantly lowered fluorescence quantum yields and lifetimes. However, this interaction did not restrict the formation of excited singlet and triplet states and hence the formation of singlet oxygen required for photocatalysis. The conjugates showed significantly higher singlet oxygen quantum yields and therefore enhanced photocatalytic activity compared to the phthalocyanines. The zinc phthalocyanines and their gold nanoparticle conjugates were successfully incorporated into electrospun polymer fibers. Spectral characteristics of the functionalized electrospun fibers indicated that the phthalocyanines and phthalocyanine-gold nanoparticle conjugates were bound and their integrity was maintained within the polymeric fiber matrices. The photophysical and photochemical properties of the complexes were equally maintained within the electrospun fibers. The functionalized fibers were applied for the photoconversion of 4-chlorophenol and Orange G as model organic pollutants. , Microsoft� Word 2010 , Adobe Acrobat 9.53 Paper Capture Plug-in
- Full Text:
- Date Issued: 2013
- Authors: Tombe, Sekai Lana
- Date: 2013
- Subjects: Phthalocyanines , Gold , Zinc , Nanoparticles , Bioconjugates , Photochemistry , Photocatalysis , Electrospinning , Polymers , Pollutants , Phenols , Azo dyes
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:4293 , http://hdl.handle.net/10962/d1004517 , Phthalocyanines , Gold , Zinc , Nanoparticles , Bioconjugates , Photochemistry , Photocatalysis , Electrospinning , Polymers , Pollutants , Phenols , Azo dyes
- Description: This work presents the syntheses, photophysical and photochemical characterization of arylthio zinc phthalocyanines and their gold nanoparticle conjugates. Spectroscopic and microscopic studies confirmed the formation of the phthalocyanine-gold nanoparticle conjugates which exhibited enhanced photophysicochemical properties in comparison to the phthalocyanines. The studies showed that the presence of gold nanoparticles significantly lowered fluorescence quantum yields and lifetimes. However, this interaction did not restrict the formation of excited singlet and triplet states and hence the formation of singlet oxygen required for photocatalysis. The conjugates showed significantly higher singlet oxygen quantum yields and therefore enhanced photocatalytic activity compared to the phthalocyanines. The zinc phthalocyanines and their gold nanoparticle conjugates were successfully incorporated into electrospun polymer fibers. Spectral characteristics of the functionalized electrospun fibers indicated that the phthalocyanines and phthalocyanine-gold nanoparticle conjugates were bound and their integrity was maintained within the polymeric fiber matrices. The photophysical and photochemical properties of the complexes were equally maintained within the electrospun fibers. The functionalized fibers were applied for the photoconversion of 4-chlorophenol and Orange G as model organic pollutants. , Microsoft� Word 2010 , Adobe Acrobat 9.53 Paper Capture Plug-in
- Full Text:
- Date Issued: 2013
Removal and photocatalysis of 4-Nitrophenol using metallophthalocyanines
- Authors: Marais, Eloïse Ann
- Date: 2008
- Subjects: Photocatalysis , Catalysis , Electrochemistry , Nitrophenols , Phthalocyanines
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:4343 , http://hdl.handle.net/10962/d1005005 , Photocatalysis , Catalysis , Electrochemistry , Nitrophenols , Phthalocyanines
- Description: Photodegradation of 4-nitrophenol (4-Np) in the presence of water-soluble zinc phthalocyanines and water-insoluble metallophthalocyanines is reported. The water-soluble phthalocyanines employed include zinc tetrasulphophthalocyanine (ZnPcS[subscript 4]), zinc octacarboxyphthalocyanine (ZnPc(COOH)[subscript 8]) and a sulphonated ZnPc containing a mixture of differently sulphonated derivatives (ZnPcS[subscript mix]), while the water-insoluble phthalocyanines used include unsubstituted magnesium (MgPc), zinc (ZnPc) and chloroaluminium (ClAlPc) phthalocyanine complexes and the ring-substituted zinc tetranitro (ZnPc(NO[subscript 2])[subscript 4]), zinc tetraamino (ZnPc(NH[subscript 2])[subscript 4]), zinc hexadecafluoro (ZnPcF[subscript 16]) and zinc hexadecachloro (ZnPcCl[subscript 16]) phthalocyanines. The most effective water-soluble photocatalyst is ZnPcS[subscript mix] in terms of the high quantum yield obtained for 4-Np degradation (Φ[subscript 4-Np]) as well as its photostability. While ZnPc(COOH)[subscript 8] has the highest Φ[subscript 4-Np] value relative to the other water-soluble complexes, it degrades readily during photocatalysis. The Φ[subscript 4-Np] values were closely related to the singlet oxygen quantum yields Φ[subscript Δ] and hence aggregation. The rate constants for the reaction with 4-Np were kr = 0.67 x 10[superscript 6] mol[superscript -1] dm[superscript 3] s[superscript -1] for ZnPcS[subscript mix] and 7.7 x 10[superscript 6] mol[superscript -1] dm[superscript 3] s[superscript -1] for ZnPc(COOH)[subscript 8]. ClAlPc is the most effective photocatalyst relative to the other heterogeneous photocatalysts for the phototransformation of 4-Np, with 89 ± 8.4 % degradation of 4-Np achieved after 100 min. The least effective catalysts were ZnPcCl[subscript 16] and MgPc. The final products of the photocatalysis of 4-Np in the presence of the homogeneous photocatalysts include 4-nitrocatechol and hydroquinone, while degradation of 4-Np in the presence of the heterogeneous photocatalysts resulted in fumaric acid and 4-nitrocatechol. ClAlPc was employed for the heterogeneous photocatalysis of the non-systemic insecticide, methyl paraoxon. Complete degradation of the pesticide was confirmed by the disappearance of the HPLC trace for methyl paraoxon after 100 min of irradiation with visible light. The removal of 4-Np from an aqueous medium using commercially available Amberlite[superscript ®] IRA-900 modified with metal phthalocyanines was also investigated. The metallophthalocyanines immobilised onto the surface of Amberlite[superscript ®] IRA-900 include Fe (FePcS[subscript 4]), Co (CoPcS[subscript 4]) and Ni (NiPcS[subscript 4]) tetrasulphophthalocyanines, and differently sulphonated phthalocyanine mixtures of Fe (FePcS[subscript mix]), Co (CoPcS[subscript mix]) and Ni (NiPcS[subscript mix]). Adsorption rates were fastest for the modified adsorbents at pH 9. Using the Langmuir-Hinshelwood kinetic model, the complexes showed the following order of 4-Np adsorption: CoPcS[subscript mix] > NiPcS[subscript 4] > NiPcS[subscript mix] > FePcS[subscript 4] > FePcS[subscript mix] > CoPcS[subscript 4]. The adsorbents were regenerated using dilute HNO[subscript 3], with 76 % (7.6 x 10[superscript -5] mol) of 4-Np recovered within 150 min.
- Full Text:
- Date Issued: 2008
- Authors: Marais, Eloïse Ann
- Date: 2008
- Subjects: Photocatalysis , Catalysis , Electrochemistry , Nitrophenols , Phthalocyanines
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:4343 , http://hdl.handle.net/10962/d1005005 , Photocatalysis , Catalysis , Electrochemistry , Nitrophenols , Phthalocyanines
- Description: Photodegradation of 4-nitrophenol (4-Np) in the presence of water-soluble zinc phthalocyanines and water-insoluble metallophthalocyanines is reported. The water-soluble phthalocyanines employed include zinc tetrasulphophthalocyanine (ZnPcS[subscript 4]), zinc octacarboxyphthalocyanine (ZnPc(COOH)[subscript 8]) and a sulphonated ZnPc containing a mixture of differently sulphonated derivatives (ZnPcS[subscript mix]), while the water-insoluble phthalocyanines used include unsubstituted magnesium (MgPc), zinc (ZnPc) and chloroaluminium (ClAlPc) phthalocyanine complexes and the ring-substituted zinc tetranitro (ZnPc(NO[subscript 2])[subscript 4]), zinc tetraamino (ZnPc(NH[subscript 2])[subscript 4]), zinc hexadecafluoro (ZnPcF[subscript 16]) and zinc hexadecachloro (ZnPcCl[subscript 16]) phthalocyanines. The most effective water-soluble photocatalyst is ZnPcS[subscript mix] in terms of the high quantum yield obtained for 4-Np degradation (Φ[subscript 4-Np]) as well as its photostability. While ZnPc(COOH)[subscript 8] has the highest Φ[subscript 4-Np] value relative to the other water-soluble complexes, it degrades readily during photocatalysis. The Φ[subscript 4-Np] values were closely related to the singlet oxygen quantum yields Φ[subscript Δ] and hence aggregation. The rate constants for the reaction with 4-Np were kr = 0.67 x 10[superscript 6] mol[superscript -1] dm[superscript 3] s[superscript -1] for ZnPcS[subscript mix] and 7.7 x 10[superscript 6] mol[superscript -1] dm[superscript 3] s[superscript -1] for ZnPc(COOH)[subscript 8]. ClAlPc is the most effective photocatalyst relative to the other heterogeneous photocatalysts for the phototransformation of 4-Np, with 89 ± 8.4 % degradation of 4-Np achieved after 100 min. The least effective catalysts were ZnPcCl[subscript 16] and MgPc. The final products of the photocatalysis of 4-Np in the presence of the homogeneous photocatalysts include 4-nitrocatechol and hydroquinone, while degradation of 4-Np in the presence of the heterogeneous photocatalysts resulted in fumaric acid and 4-nitrocatechol. ClAlPc was employed for the heterogeneous photocatalysis of the non-systemic insecticide, methyl paraoxon. Complete degradation of the pesticide was confirmed by the disappearance of the HPLC trace for methyl paraoxon after 100 min of irradiation with visible light. The removal of 4-Np from an aqueous medium using commercially available Amberlite[superscript ®] IRA-900 modified with metal phthalocyanines was also investigated. The metallophthalocyanines immobilised onto the surface of Amberlite[superscript ®] IRA-900 include Fe (FePcS[subscript 4]), Co (CoPcS[subscript 4]) and Ni (NiPcS[subscript 4]) tetrasulphophthalocyanines, and differently sulphonated phthalocyanine mixtures of Fe (FePcS[subscript mix]), Co (CoPcS[subscript mix]) and Ni (NiPcS[subscript mix]). Adsorption rates were fastest for the modified adsorbents at pH 9. Using the Langmuir-Hinshelwood kinetic model, the complexes showed the following order of 4-Np adsorption: CoPcS[subscript mix] > NiPcS[subscript 4] > NiPcS[subscript mix] > FePcS[subscript 4] > FePcS[subscript mix] > CoPcS[subscript 4]. The adsorbents were regenerated using dilute HNO[subscript 3], with 76 % (7.6 x 10[superscript -5] mol) of 4-Np recovered within 150 min.
- Full Text:
- Date Issued: 2008
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