ORCID Profile
0000-0002-0241-0543
Current Organisation
RMIT University
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In Research Link Australia (RLA), "Research Topics" refer to ANZSRC FOR and SEO codes. These topics are either sourced from ANZSRC FOR and SEO codes listed in researchers' related grants or generated by a large language model (LLM) based on their publications.
Nanotechnology | Synthesis of Materials | Nanotechnology | Functional Materials | Catalysis and Mechanisms of Reactions | Solid State Chemistry | Chemistry Of Catalysis | Organic Chemical Synthesis | Materials Engineering | Chemical Characterisation of Materials | Physical Chemistry (Incl. Structural) | Environmental Technologies | Ore Deposit Petrology
Expanding Knowledge in the Chemical Sciences | Energy transformation not elsewhere classified | Urban and Industrial Water Management | Land and water management | Air quality | Industrial Chemicals and Related Products not elsewhere classified | Earth sciences | Chemical sciences | Other |
Publisher: Royal Society of Chemistry (RSC)
Date: 2007
DOI: 10.1039/B618280A
Publisher: Elsevier BV
Date: 09-2022
Publisher: Elsevier BV
Date: 05-2008
DOI: 10.1016/J.CHEMOSPHERE.2008.01.061
Abstract: The photocatalytic removal of humic acid (HA) using TiO2 under UVA irradiation was examined by monitoring changes in the UV(254) absorbance, dissolved organic carbon (DOC) concentration, apparent molecular weight distribution, and trihalomethane formation potentials (THMFPs) over treatment time. A resin fractionation technique in which the s les were fractionated into four components: very hydrophobic acids (VHA), slightly hydrophobic acids, hydrophilic charged (CHA) and hydrophilic neutral (NEU) was also employed to elucidate the changes in the chemical nature of the HA components during treatment. The UVA/TiO2 process was found to be effective in removing more than 80% DOC and 90% UV(254) absorbance. The THMFPs of s les were decreased to below 20 microg l(-1) after treatments, which demonstrate the potential to meet increasingly stringent regulatory level of trihalomethanes in water. Resin fractionation analysis showed that the VHA fraction was decreased considerably as a result of photocatalytic treatments, forming CHA intermediates which were further degraded with increased irradiation time. The NEU fraction, which comprised of non-UV-absorbing low molecular weight compounds, was found to be the most persistent component.
Publisher: IWA Publishing
Date: 08-2004
Abstract: A photoreactor has been set up to study the photodegradation of volatile organic compound (VOC) in situ. In the reactor, TiO2 and Pt/TiO2 photocatalysts were immobilized on to UV-transparent quartz support. Scanning electron microscope (SEM) studies and Brunauer-Emmett-Teller (BET) surface area measurements revealed that the quartz fiber support was mostly coated with catalyst with a total surface area of 4.0 ± 0.3 m2/g. The photocatalytic activity of the photocatalysts was evaluated for the photodegradation of 160 ppm toluene-laden air. It was found that 50-70% of toluene was degraded within the first 5 min of UV illumination. Both TiO2 and Pt/TiO2 photocatalysts suffered from deactivation after 18 hours of continuous operation, and the photocatalysts' activity was significantly reduced. However, platinization doubled the photocatalyst life and delayed the onset of de-activation. The presence of moisture was found to shift the onset of catalyst de-activation to an earlier time. It is concluded that the de-activation of the photocatalyst was due to the accumulation of intermediates on the photocatalysts surface preventing the toluene being adsorbed on the photocatalyst surface for degradation.
Publisher: Royal Society of Chemistry (RSC)
Date: 2023
DOI: 10.1039/D3TA01379K
Abstract: An electrocatalyst with trace vanadium alloyed with liquid metal reduces CO 2 directly into solid carbon.
Publisher: Elsevier BV
Date: 05-2007
Publisher: Elsevier BV
Date: 02-2007
Publisher: Elsevier BV
Date: 06-2005
Publisher: Elsevier BV
Date: 2008
Publisher: Elsevier BV
Date: 12-2021
Publisher: Royal Society of Chemistry (RSC)
Date: 07-2014
DOI: 10.1039/C4DT01123F
Abstract: Successful synthesis of stable MFe2O4 nanoparticles@C has been realized by applying the novel concept of using levulinic acid possessing carboxyl and carbonyl groups to facilitate the interaction with metal ions (M(2+) and Fe(3+)) and the carbon source (phloroglucinol) in the sol-gel polymerization method. All the s les have been characterized by XRD, SEM, FT-IR, TEM, HRTEM, ICP-AES, CHNS, and N2 adsorption-desorption, and were studied for their performance towards hydrogenation reaction of styrene. Out of three s les NiFe2O4 gave excellent selective hydrogenation activity of styrene to ethyl benzene (100% conversion and 100% selectivity). Optimal production of ethyl benzene over NiFe2O4 nanoparticles@C has been established at 80 °C reaction temperature after 24 h reaction time under 40 bar hydrogen pressure.
Publisher: Wiley
Date: 30-10-2023
Publisher: Informa UK Limited
Date: 05-2007
Publisher: Elsevier BV
Date: 05-2020
Publisher: Elsevier BV
Date: 03-2019
Publisher: Elsevier BV
Date: 10-09-2005
Publisher: Elsevier BV
Date: 09-2006
Publisher: Elsevier BV
Date: 12-2017
Publisher: Elsevier BV
Date: 2008
Publisher: Elsevier BV
Date: 02-2003
Publisher: American Chemical Society (ACS)
Date: 07-10-2010
DOI: 10.1021/LA902592P
Abstract: A nonaqueous photodeposition procedure for forming Au nanoparticles on semiconducting supports (TiO(2), CeO(2), and ZrO(2)) was investigated. Intrinsic excitation of the support was sufficient to induce Au(0) nucleation, without the need for an organic hole-scavenging species. Photoreduction rates were higher over TiO(2) and ZrO(2) than over CeO(2), likely due to a lower rate of photogenerated electron recombination. Illumination resulted in metallization of the adsorbed Au species and formation of crystalline Au nanoparticles dispersed across the oxide surfaces. On the basis of transmission electron microscopy (TEM) evidence of a strong Au particle-metal oxide interaction, it is proposed that Au deposit formation proceeds via the nucleation of highly dispersed clusters which can diffuse and amalgamate at room temperature to form larger surface-defect-immobilized clusters, with the final particle size being significantly smaller than that achieved by conventional aqueous photodeposition. From this work, it is possible to draw several new fundamental insights, with regards to both the nonaqueous photodeposition process and the general mechanism by which dispersed metallic Au nanoparticles are formed from ionic precursors adsorbed upon metal oxide supports.
Publisher: Elsevier BV
Date: 04-2004
Publisher: Elsevier BV
Date: 05-2020
DOI: 10.1016/J.JHAZMAT.2019.121827
Abstract: In this work we report the production of Bi
Publisher: IEEE
Date: 2008
Publisher: Elsevier BV
Date: 28-01-2005
Publisher: Elsevier BV
Date: 03-2007
Publisher: Inderscience Publishers
Date: 2007
Publisher: Elsevier BV
Date: 03-2007
Publisher: Wiley
Date: 16-06-2021
DOI: 10.1002/JCTB.6815
Abstract: We report our recent study on the use of a zinc‐modified NaY zeolite to decompose CO 2 at a temperature range between 300 and 550 °C. At a reaction temperature of 450 °C, we observed that 70% of CO 2 was converted with an insignificant quantity of CO produced. Scanning electron microscopy and Fourier transform infrared spectroscopic analysis of the neat and spent catalysts confirmed the presence of carbon nanostructures after the reaction. In addition to this, CHN analysis supports these results by providing weight percent (0.73 wt%) of carbon after reaction. Stability of the catalyst was further confirmed with slight/no change in X‐ray diffraction technique. This route potentially offers a facile strategy to achieve CO 2 decomposition and an explanation of the formation of carbon on zinc‐modified zeolite catalysts. © 2021 Society of Chemical Industry (SCI).
Publisher: Elsevier BV
Date: 04-2010
Publisher: Springer Science and Business Media LLC
Date: 08-2007
DOI: 10.1039/B703528D
Abstract: By identifying the Electron Partitioning Effect (EPE) as responsible for the large gold deposits usually formed in the conventional photodeposition method, a low energy UV light-based method for the preparation of comparatively high-activity gold-titania catalysts was developed. These materials were tested in the carbon monoxide (CO) oxidation reaction and returned markedly higher levels of activity at room temperature, when compared to catalysts prepared by the traditional photodeposition method. This is the first instance of using a light-mediated process for preparing catalysts active for the CO oxidation reaction.
Publisher: Elsevier BV
Date: 11-2020
Publisher: Elsevier BV
Date: 08-2017
Publisher: Elsevier BV
Date: 09-2006
Publisher: Springer Science and Business Media LLC
Date: 08-2005
DOI: 10.1039/B506320E
Abstract: The superiority of silver deposited titania particles over bare titania particles for the photocatalytic oxidation of selected organic compounds is explained: the presence of silver mainly enhances the photocatalytic oxidation of organic compounds that are predominantly oxidised by holes, while it has only an insignificant effect on those organic compounds that require hydroxyl radicals for their mineralisation.
Publisher: Royal Society of Chemistry (RSC)
Date: 2022
DOI: 10.1039/D1EE03283F
Abstract: We present a simple alternative pathway to transform carbon dioxide to perpetually stored solid carbon.
Publisher: Elsevier BV
Date: 2015
Publisher: Elsevier BV
Date: 07-2023
Publisher: Elsevier BV
Date: 08-2021
Publisher: Elsevier BV
Date: 07-2022
Publisher: Elsevier BV
Date: 2007
Publisher: IEEE
Date: 2008
Publisher: American Scientific Publishers
Date: 04-2006
DOI: 10.1166/JBN.2006.006
Publisher: Elsevier BV
Date: 11-2022
Publisher: Elsevier BV
Date: 2022
Publisher: Elsevier BV
Date: 10-2005
Publisher: Elsevier BV
Date: 11-2020
Publisher: Elsevier BV
Date: 04-2006
Publisher: Elsevier BV
Date: 10-2002
Publisher: American Chemical Society (ACS)
Date: 03-2022
Publisher: Springer Science and Business Media LLC
Date: 05-02-2008
Start Date: 02-2018
End Date: 12-2022
Amount: $402,934.00
Funder: Australian Research Council
View Funded ActivityStart Date: 01-2007
End Date: 12-2012
Amount: $180,000.00
Funder: Australian Research Council
View Funded ActivityStart Date: 04-2021
End Date: 12-2023
Amount: $975,934.00
Funder: Australian Research Council
View Funded ActivityStart Date: 01-2006
End Date: 10-2007
Amount: $200,000.00
Funder: Australian Research Council
View Funded Activity