ORCID Profile
0000-0001-8920-5667
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Publisher: Elsevier BV
Date: 07-2018
Publisher: Elsevier BV
Date: 2018
Publisher: MDPI AG
Date: 24-05-2023
DOI: 10.20944/PREPRINTS202305.1685.V1
Abstract: Isotope detection and identification is paramount in many fields of science and industry, such as in the fusion and fission energy sector, in medicine and material science, and in archeology. The isotopic information provides fundamental insight on the research questions related to these fields as well as insight on product quality and operational safety. However, isotope identification with the established mass-spectrometric methods is laborious and requires laboratory conditions. In this work, Microwave-Assisted Laser-Induced Breakdown Spectroscopy (MW-LIBS) is introduced for isotope detection and identification utilizing radical and molecular emission. The approach is demonstrated with stable B and Cl isotopes in solids and H isotopes in liquid using emission from BO and BO2, CaCl, and OH molecules, respectively. MW-LIBS utilizes the extended emissive plasma lifetime and molecular emission signal integration times up to 900 s to enable use of low ~4 mJ ablation energy without compromising signal intensity and, consequently, sensitivity. On the other hand, long plasma lifetime gives time for molecular formation. Increase in the signal intensity towards the late microwave-assisted plasma was prominent in BO2 and OH emission intensities. As MW-LIBS is online-capable and requires minimal s le preparation, it is an interesting option for isotope detection in various applications.
Publisher: American Chemical Society (ACS)
Date: 15-10-2008
DOI: 10.1021/ES801087F
Abstract: The effects of passing ozone over different zeolite and MCM-41 materials to remove toluene were investigated. Different ozone-to-toluene ratios were used to evaluate the catalytic performance during ozonation. The micro- and meso-porous materials removed about 50% of the toluene via adsorption and another 20-40% was decomposed by ozonation, which was catalytically enhanced by the zeolite and MCM-41 materials. The catalytic reaction portion increased by using a higher ozone inlet concentration and it was further enhanced to around 50% with the use of more adsorbents or with longer residence times. Inside the porous structure of the material, ozone was either decomposed into active atomic oxygen for reactions or converted into oxygen for active site regeneration. The number of Lewis acid sites in the adsorbents for ozone decomposition and byproduct generation during the reactions limit the catalytic activities. Trace amounts of intermediates including aldehydes and organic acids were quantified in the ozonation process. A higher ozone inlet concentration helped to reduce intermediate species formation but it led to more residual ozone in the exhaust. The high adsorption capability of the zeolite and MCM-41 adsorbents could serve as reservoirs for suppressing the release of intermediate species to the exhaust.
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C6EE90016J
Abstract: Correction for ‘2D phosphorene as a water splitting photocatalyst: fundamentals to applications’ by Mohammad Ziaur Rahman et al. , Energy Environ. Sci. , 2016, 9 , 709–728.
Publisher: American Scientific Publishers
Date: 04-2012
Abstract: Crystalline Co3O4 nanowire arrays freely supported on Ni foam are successfully synthesized using a template-free method. The effects of reaction time, concentration of reactants, and temperature on the morphology of the nanowires are studied. The results indicate that uniform Co3O4 nanowires could be synthesized at 90 degrees C, and a transformation of the s les' morphology from nanoparticles to nanowires to microrods is observed by controlling the concentration of the reactants. The well-ordered nanowires synthesized under the selected reaction conditions are composed of spinel Co3O4 with diameters of 500-580 nm and lengths of 6-8 microm. These nanowires show good catalytic activity for the ozone catalytic oxidation of toluene.
Publisher: MDPI AG
Date: 08-2023
Abstract: Isotope detection and identification is paramount in many fields of science and industry, such as in the fusion and fission energy sector, in medicine and material science, and in archeology. Isotopic information provides fundamental insight into the research questions related to these fields, as well as insight into product quality and operational safety. However, isotope identification with established mass-spectrometric methods is laborious and requires laboratory conditions. In this work, microwave-assisted laser-induced breakdown spectroscopy (MW-LIBS) is introduced for isotope detection and identification utilizing radical and molecular emission. The approach is demonstrated with stable B and Cl isotopes in solids and H isotopes in liquid using emissions from BO and BO2, CaCl, and OH molecules, respectively. MW-LIBS utilizes the extended emissive plasma lifetime and molecular-emission signal-integration times up to 900 μs to enable the use of low (~4 mJ) ablation energy without compromising signal intensity and, consequently, sensitivity. On the other hand, long plasma lifetime gives time for molecular formation. Increase in signal intensity towards the late microwave-assisted plasma was prominent in BO2 and OH emission intensities. As MW-LIBS is online-capable and requires minimal s le preparation, it is an interesting option for isotope detection in various applications.
Publisher: ASMEDC
Date: 2007
DOI: 10.1115/ES2007-36159
Abstract: In many Asian countries Coal is frequently used a major fuel in power plants. Burning coal creates quite a lot of environmental problems when compared to other cleaner fuels such as natural gas. Experimental study of co-combustion of coal and biomass was conducted in a laboratory scale combustion facility to evaluate the combustion and pollutant emission performance under different operation parameters. Rice husk and bamboo were used as the biomass fuels in this study. This paper reported the influence of the biomass blending ratio in the fuel mixture and the excess air ratio on the combustion behavior. It was noted that the combustion temperature and the energy output from the co-firing process were reduced compared to coal combustion alone owing to the fact that biomass has lower heating value compared to coal. However, the high volatile matter (VM) content of biomass improved the combustion time scale so that the carbon monoxide (CO) emissions were reduced substantially. In addition, the fuel nitrogen and sulfur content in biomass were lower than that of coal and hence suppressed the formation of nitrogen oxides (NOx) and sulfur dioxide (SO2) during the cocombustion process. The increase of excess air ratio also affected most of the pollutant emissions. The pollutant emission per unit energy output at different excess air ratios and biomass blending ratios were studied in detail in this paper. Attention should be paid to the high potential of slagging and fouling in the boiler when co-firing coal with biomass.
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C5EE03732H
Abstract: In this review, we focus on analysing the fundamental electronic, optical and chemical properties of 2D phosphorene to assess its suitability as a metal-free water splitting photocatalyst.
Publisher: MDPI AG
Date: 09-04-2019
DOI: 10.3390/SOILSYSTEMS3020027
Abstract: Grapevine cane and stalks were considered for pyrolysis at 400 to 700 °C to produce biochar for increasing the water holding capacity of vineyard soil. Feedstocks were pyrolysed using a continuous feed reactor and the resulting biochars characterized in terms of physico-chemical properties, including water retention performance. Hydrophobicity was found in biochar from both feedstocks pyrolysed at 400 °C, but not at higher temperatures. At low soil matric potential, the pyrolysis temperature was the defining variable in determining water retention whereas at higher pressures, the feedstock was the more important variable. Available water content (AWC) of biochar increased with increasing pyrolysis temperatures, with optimal results obtained from grapevine cane at a pyrolysis temperature of 700 °C, which had an AWC 23% higher than a typical clay type soil. Principal component analysis showed variability in water retention of these biochars to be closely associated with the zeta potential, as well as the carbon and ionic content, suggesting that surface charge and hydrophobicity are key properties determining water holding capacity. Pure biochars were superior in water retention performance to typical sandy soils, and so biochar amendment of these soil types may improve water holding (particularly at field capacity). Further study with pot or field trials is recommended to confirm water retention behaviour and assess the feasibility of application under different viticultural scenarios.
Publisher: Elsevier BV
Date: 02-2010
DOI: 10.1016/J.BIORTECH.2009.09.008
Abstract: Experiments were conducted in a continuous flow reactor at room temperature to evaluate the elimination of low-concentration toluene in the gas phase to verify if fly-ash products from biomass combustion in an ozonation system could be used in the removal of volatile organic compounds. The fly-ash products from pure biomass combustion (Ash(100)) demonstrated the highest ozonation activities upon the removal of low-concentration toluene (1.5 ppmv), followed by the fly-ash products from co-combustion (Ash(30)) and the coal combustion (Ash(0)). Kinetic experiments showed that the activation energy of the toluene elimination process was substantially reduced with the use of ozone and the reaction intermediates, such as formic acids, aldehydes, etc. Results also showed that the intermediates were reduced with increasing humidity level. The combined use of fly-ash products and zeolite 13X enhanced the removal of toluene to above 90% and suppressed the release of residual ozone and intermediates by holding them in the adsorbed phase.
Publisher: American Chemical Society (ACS)
Date: 10-08-2015
Publisher: Elsevier BV
Date: 08-2017
Publisher: Informa UK Limited
Date: 22-09-2010
Publisher: Elsevier BV
Date: 11-2007
Publisher: Elsevier BV
Date: 03-2013
Publisher: Elsevier BV
Date: 08-2020
Publisher: Royal Society of Chemistry (RSC)
Date: 2010
DOI: 10.1039/C002669G
Publisher: Springer Science and Business Media LLC
Date: 09-2014
Publisher: Elsevier BV
Date: 10-2018
Publisher: Elsevier BV
Date: 09-2013
Publisher: Elsevier BV
Date: 04-2008
Publisher: American Chemical Society (ACS)
Date: 22-12-2015
Publisher: Elsevier BV
Date: 07-2018
DOI: 10.1016/J.WASMAN.2018.05.004
Abstract: The co-production of biochar and bioenergy using pyrolysis-combustion processes can potentially minimize the emission problems associated with conventional methods of agricultural by-product disposal. This approach also provides significant added-value potential through biochar application to soil. Despite these advantages, variations in biomass composition, including sulfur, nitrogen, ash, and volatile matter (VM) content, may significantly influence both the biochar quality and the emissions of harmful particulate matter (PM) and gaseous pollutants (SO
Publisher: Elsevier BV
Date: 07-2013
DOI: 10.1016/J.BIORTECH.2013.04.070
Abstract: Cu, Ni and Fe oxides supported on ceria were investigated for their performance as oxygen carriers during the chemical looping combustion of biomass-derived syngas. A complex gas mixture containing CO, H2, CO2, CH4 and other hydrocarbons was used to simulate the complex fuel gas environment derived from biomass gasification. Results show that the transfer of the stored oxygen into oxidants for the supported Cu and Ni oxides at 800°C for the combustion of syngas was effective (>85%). The unsupported Cu oxide showed high oxygen carrying capacity but particle sintering was observed at 800°C. A reaction temperature of 950°C was required for the supported Fe oxides to transfer the stored oxygen into oxidants effectively. Also, for the complex fuel gas environment, the supported Ni oxide was somewhat effective in reforming CH4 and other light hydrocarbons into CO, which may have benefits for the reduction of tar produced during biomass pyrolysis.
Publisher: American Chemical Society (ACS)
Date: 24-02-2015
DOI: 10.1021/EF502422T
Publisher: Elsevier BV
Date: 03-2008
Publisher: Elsevier BV
Date: 11-2017
DOI: 10.1016/J.BIORTECH.2017.08.091
Abstract: The aim of this study was to evaluate the emissions of polycyclic aromatic hydrocarbons (PAHs) bound to the particulate matter (PM) during the combustion of raw pyrolysis volatiles (bio-oil and pyrogas mixture) generated from the pyrolysis of rice husk. Five different raw pyrolysis volatiles were produced at varying pyrolysis temperatures (400-800°C) and subsequently combusted in a laboratory-scale, continuous pyrolysis-combustion facility at 850°C. 15 priority pollutant PAH levels in the resulting biochar, bio-oil, and PM were evaluated. Results showed that combustion of the raw pyrolysis volatiles produced at elevated pyrolysis temperatures resulted in greater concentrations of PM-bound PAHs (119% increase between 400 and 800°C) due to the increased PAH and oxy-aromatic content of the bio-oil fraction. Significantly increased benzo(a)pyrene (BaP) - equivalent toxicity of the biochar and PM was observed at elevated pyrolysis temperatures.
Publisher: AIP Publishing
Date: 18-06-2018
DOI: 10.1063/1.5038785
Abstract: Photoinduced charge separation against their faster recombination is a rate determinant for photocatalytic proton reduction to hydrogen. Dissociation of electron-hole pairs into free electrons and holes in carbon nitrides greatly suffered from the inherent high recombination rate. This study has shown that coupling two energetically optimized, but with different phases carbon nitrides in the form of hybrid could significantly inhibit the charge carrier recombination and facilitate the overall charge transfer processes. It is also found that the potential gradient in this homojunction delocalizes electrons and holes, and increases the spatial charge separation. Therefore, this leads to a record high apparent quantum efficiency of 5% for photocatalytic H2 production from water under visible light irradiation in the absence of a precious metal (e.g., Pt) cocatalyst.
Publisher: American Chemical Society (ACS)
Date: 14-02-2020
Publisher: American Chemical Society (ACS)
Date: 06-04-2015
Publisher: ASMEDC
Date: 2007
Abstract: This study investigated the performance of multi-transition metal (Cu, Cr, Ni and Co) ions exchanged zeolite 13X catalysts on methane emission abatement, especially at methane level of the exhaust from natural gas fueled vehicles. Catalytic activity of methane combustion using multi-ions exchanged catalyst was studied under different parameters: mole % of metal loading, inlet velocity and inlet methane concentration at atmospheric pressure and 500 °C. Performance of the catalysts was investigated and explained in terms of the apparent activation energy, number of active sites and BET surface area of the catalyst. This study showed that the multi-ions exchanged catalyst outperformed the single-ions exchanged and the acidified 13X catalysts. Lengthening the residence time could also lead to higher methane conversion %. Catalytic activity of the catalysts was influenced by the mole % of metal loading which played important roles in affecting the apparent activation energy of methane combustion, active sites and also the BET surface area of the catalyst. Increasing mole % of metal loading in the catalyst decreased the apparent activation energy for methane combustion and also the BET surface area of the catalyst. In view of these, there existed an optimized mole % of metal loading where the highest catalytic activity was observed.
Publisher: Elsevier BV
Date: 06-2020
Publisher: ASMEDC
Date: 2009
DOI: 10.1115/ES2009-90128
Abstract: The potential use of biomass co-combustion derived fly-ash products and zeolite 13X for the elimination of volatile organic compounds (VOCs) using ozone was investigated for an integrated solar-assisted air purification and desiccant cooling system. Fly-ash products from rice husk-coal co-combustion at different biomass blending ratios were used as the adsorbent/catalyst materials. The material characteristics of the adsorbent/catalyst materials such as metal content and surface area were compared and correlated with the catalytic activities. It was found that the surface area and the metal constitutes have made the catalytic activities over the fly-ash products from biomass co-combustion superior to that from coal-only combustion. The elevated reaction temperatures from 25°C to 75°C also have significant effects on the removal of VOCs. The apparent activation energies of the reaction path over the fly-ash products with the addition of ozone to the air were reduced, when compared with the use of air as an oxidant. On the other hand, the potential synergy to Zeolite 13X was explored. The combined catalytic ozonation and adsorption enhanced the VOCs removal and at the same time reduced the intermediates emission. Furthermore, the hydrophilic properties of zeolite 13X could be utilized to handle the latent load of the solar-assisted ventilation system for energy conservations.
Publisher: Elsevier BV
Date: 2008
DOI: 10.1016/J.BIORTECH.2006.11.051
Abstract: The potential of co-firing rice husk and bamboo with coal was studied in a bench-scale pulverized fuel combustion reactor. Experimental parameters including biomass blending ratio in the fuel mixture, biomass grinding size, excess air ratio and relative moisture content in the biomass were investigated. Particulate Matters in the forms of PM(10), PM(2.1), ultra fine particles as well as the associated Polycyclic Aromatic Hydrocarbons (PAHs) emissions were evaluated. An operation range between 10% and 30% of biomass to coal ratio was found to be the optimum range in terms of minimum pollutant emissions per unit energy output. Co-combustion of coal with biomass seemed to have the effect of moving the fly-ash in PM(2.1) to a larger size range, but increasing the number counts of the ultra fine particles. It was noted that the much higher volatile matter content in the biomass fuels has played a key role in improving the combustion performance in the system. However, slagging, fouling and formation of clinker could be the issues requiring attention when using biomass co-combustion in conventional boilers.
Publisher: Elsevier BV
Date: 11-2017
Publisher: Elsevier BV
Date: 05-2007
DOI: 10.1016/J.JHAZMAT.2006.08.077
Abstract: This study investigated the performance of a combined ozone and zeolite system in eliminating gaseous toluene which is a major contaminant in many industrial and indoor environments. The hypothesis that the removal of toluene by ozone can be substantially affected by confining the oxidation reaction in a zeolite structure was evaluated. The degradation of toluene seemed to be contributed by the active oxygen atom generated from the decomposition of ozone at the Lewis acid sites in the zeolite 13X. Air containing toluene levels at 1.5, 2 and 3 ppm was injected with ozone in the range of 0-6 ppm before being vented into a fixed amount of 3600 g zeolite 13X with 90 mm bed-length. The experimental results showed that the elimination rate of toluene was significantly enhanced when compared to using zeolite or ozone alone. In particular, over 90% of the 1.5 ppm toluene was removed when 6 ppm ozone was used at 40% relative humidity level. Deactivation of the zeolite 13X after a few hours of reactions under the current experimental conditions was probably due to the adsorbed water, carbon dioxide and the reaction by-products. The residue species left in the zeolite and the intermediate species in the exhaust gas stream were characterized by FT-IR, GC-MS and HP-LC methods, respectively. A distinctive peak of O atom attached to the Lewis acid site at 1380 cm(-1) was found in the FT-IR spectrum and trace amount of aldehydes was found to be the reaction by-products.
No related grants have been discovered for Chi Wai Kwong.