Pt on Atomic-Layered WO3 Islands: Electronic Tuning of Platinum-Tungsten Heterostructures for Highly Efficient Low-Temperature VOC Combustion.

Adjusting the electronic state of noble metal catalysts on a nanoscale is crucial for optimizing the performance of nanocatalysts in many important environmental catalytic reactions, particularly in volatile organic compound (VOC) combustion. This study reports a novel strategy for optimizing Pt catalysts by modifying their electronic structure to enhance the electron density of Pt. The research illustrates the optimal 0.2Pt-0.3W/Fe2O3 heterostructure with atomic-thick WO3 layers as a bulking block to electronically modify supported Pt nanoparticles. Methods such as electron microscopy, X-ray photoelectron spectroscopy, and in situ Fourier transform infrared spectroscopy confirm Pt's electron-enriched state resulting from electron transfer from atomic-thick WO3. Testing for benzene oxidation revealed enhanced low-temperature activity with moderate tungsten incorporation. Kinetic and mechanistic analyses provide insights into how the enriched electron density benefits the activation of oxygen and the adsorption of benzene on Pt sites, thereby facilitating the oxidation reaction. This pioneering work on modifying the electronic structure of supported Pt nanocatalysts establishes an innovative catalyst design approach. The electronic structure-performance-dependent relationships presented in this study assist in the rational design of efficient VOC abatement catalysts, contributing to clean energy and environmental solutions.

Enhancing Benzene Combustion Activity through Preferential Platinum Atom Exposure via Strategic Pt-Cu Alloying.

Volatile organic compounds such as benzene are hazardous air pollutants that require effective elimination. Noble metal-based catalysts exhibit high benzene combustion activity, but their prohibitive cost necessitates strategies to enhance utilization efficiency. This study investigates a Pt-Cu alloy catalyst for improved benzene combustion by preferentially exposing Pt active sites through Cu alloying. Aberration-corrected scanning transmission electron microscopy and X-ray spectroscopy characterize the nanoscale distribution and enrichment of Pt on the alloy surface. Kinetic measurements demonstrate substantially enhanced activity compared with Pt catalysts, attributed to increased Pt metallic site exposure rather than alteration of the reaction mechanism. In situ Fourier transform infrared (FTIR) spectroscopy reveals a higher abundance of terrace-like Pt sites in the alloy, beneficial for benzene adsorption. Partial pressure dependence analyses indicate competitive adsorption of benzene and O2, following Langmuir-Hinshelwood kinetics. These findings provide conceptual insights into tuning surface composition in bimetallic catalysts to optimize noble metal efficiency, with broad applicability for sustainable catalytic process advancement.

Surface design of g-C3N4 quantum dot-decorated TiO2(001) to enhance the photodegradation of indoor formaldehyde by experimental and theoretical investigation.

Formaldehyde (CHOH), a common volatile organic compound, causes many adverse effects on human health. The highly exposed TiO2(001) facet possesses a high photodegradation efficiency of CHOH due to its excellent ability to trap photogenerated holes and high density of surface unsaturated Ti atoms (Ti5c) to bind CHOH. However, the rapid recombination of photoinduced electron-hole pairs of TiO2(001) limits the photodegradation efficiency. We adopted a strategy of decorating TiO2(001) with g-C3N4 quantum dots (QDs), exploiting the quantum effect of g-C3N4QDs and their combined staggered band structure. This decoration improves the photocatalytic activity of TiO2(001). Moreover, the chemical configuration of g-C3N4QDs/TiO2(001) and the combination mode between the g-C3N4QDs and TiO2(001) support were explored in detail using high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), and density functional theory (DFT) calculations. Following the physiochemical characteristic results, the transport mechanism of photoinduced carriers was further analyzed by ultraviolet photoelectron spectroscopy (UPS), electron paramagnetic resonance (EPR), and Heyd-Scuseria-Ernzerh (HSE) exchange-correlation functional calculations. Finally, the performance and reaction mechanism of the photodegradation of CHOH by TiO2(001) and g-C3N4QDs/TiO2(001) were thoroughly investigated. The results show that the g-C3N4QDs were composed of an N-defect tri-s-triazine supported by TiO2(001) via a strong C-O-Ti chemical bond, which accelerated the separation of photoinduced carriers through a Z-scheme route. The photodegradation and mineralization efficiencies of CHOH were significantly promoted by 30% and 60% for g-C3N4QDs/TiO2(001) compared with those of TiO2(001). The photodegradation mechanism proceeded as CHOH - dioxymethylene - formate - carbonate - CO2. This study provides a surface engineering means to design highly active modified TiO2 for CHOH photodegradation.

Improvement of water resistance by Fe2O3/TiO2 photoelectrocatalysts for formaldehyde removal: experimental and theoretical investigation.

TiO2-based photocatalysts are a potential technology for removing indoor formaldehyde (CHOH) owing to their strong photooxidation ability. However, their photooxidation performance is generally weakened when suffering from the competitive adsorption of H2O. In a method inspired by the oxygen evolution reaction (OER) to generate intermediates with hydroxyl radicals on the anode electrode catalysts, an electric field was employed in this research and applied to the photooxidation of CHOH to prevent the competitive adsorption of H2O. Additionally, 0.5-5% Fe2O3 decorated TiO2 was employed to improve the photoelectrocatalytic activity. The influence of an electric field on hydroxyl-radical production was investigated by both density functional theory (DFT) with direct-imposed dipole momentum and photoelectrocatalytic experimental tests. The surface characterization of the photocatalysts, including transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance (EPR), was conducted. DFT results show that a positive electric field with a strength of 0.05 Å/V was more favorable to produce hydroxyl on Fe2O3/TiO2(010) than was a negative electric field. Fe2O3 decoration can significantly boost hydroxyl formation, resulting from a decrease in the binding energy between the Fe of Fe2O3 and the oxygen and hydrogen atoms of H2O. The dissociated hydrogen atom of the H2O preferentially remained on the catalysts' surface rather than being released into the gas flow. The experimental results demonstrated that applying 150 V could not directly enhance the photooxidation of CHOH by either TiO2 or Fe2O3/TiO2 but that it could relieve the H2O inhibitory effect by more than 10% on the Fe2O3/TiO2.

MoO3/TiO2 catalyst with atomically dispersed O-Mo-O structures toward improving NH4HSO4 poisoning resistance for selective catalytic reduction of nitrogen oxides.

Slow progress in discovering new catalysts to circumvent the problem of ammonium bisulfate (NH4HSO4, ABS) poisoning has hindered further development of selective catalytic reduction (SCR) technology of NOx with ammonia (from numerous industrial processes) in afterburning systems at temperatures below dew point of ABS (typically between 280 °C and 320 °C). Recently, we have explored the use of atomically dispersed Mo species on TiO2 particles (hereafter denoted as MoO3/TiO2) as highly efficient catalyst for NH3-SCR reaction. In the present study, it will be shown that this type of catalyst is highly resistant to ABS poisoning for NH3-SCR reaction, overcoming a major issue afflicting the application of commercial V2O5-WO3/TiO2 catalyst at temperatures below the dew point of ABS. Aberration-corrected scanning transmission electron microscopy (STEM) suggests that most of the Mo species are present in atomically dispersed form in the MoO3/TiO2 catalyst. SO2 oxidation measurements show that the MoO3/TiO2 catalyst exhibits a substantially lower SO2 oxidation rate compared to the commercial V2O5-WO3/TiO2, mitigating ABS formation. Furthermore, decomposition of ABS on MoO3/TiO2 surface is found to be extremely facile. Temperature-programmed surface reaction (TPSR) with NO shows that the decomposition temperature of ABS over MoO3/TiO2 is 70 °C lower than that found on the commercial V2O5-WO3/TiO2 catalyst. Our investigations provide valuable information for the development of NH3-SCR catalysts with exceptional resistance to ABS poisoning for NOx emission control.

Experimental and theoretical investigation of the enhancement of the photo-oxidation of Hg0 by CeO2-modified morphology-controlled anatase TiO2.

This study aims to investigate the coeffects of predominantly exposed anatase TiO2{001} and {101} and CeO2 loading on the photo-oxidation of Hg0 to relieve the adverse effects caused by higher temperatures of 50-250 °C. The effect of loading CeO2 on the photocatalytic activity of morphology-controlled TiO2 was not only investigated using DFT with U correction but also experimentally analyzed by characterizing the electrochemical properties and the formation of free radicals. The theoretical calculation showed that CeO2 loading on TiO2{101} was more stable than that on TiO2{001}. Accordingly, a larger portion of CeO2 was observed to anchor to the (101) plane than to the (001) plane. CeO2 loading is more beneficial for increasing the distribution of photo-induced electrons and holes on the surface of 7%CeTi than on the surface of TiO2 and increases the energy difference between the conduction band edge of 7%CeTi and the standard redox potential of O2/·O2-. Correspondingly, the photocatalytic removal efficiencies (PREs) of Hg0 by 7%CeTi were significantly enhanced compared with those of pristine TiO2. The effect of CeO2 was highly morphologically dependent on the photocatalytic activity. This study provides valuable insight into surface engineering strategies for morphology-controlled photocatalysts for air pollution control technology.

Coupling life cycle assessment with scenario analysis for sustainable management of Disperse blue 60.

Sustainable management of dyeing industry is of paramount importance in order to minimize resource consumption and reduce related environmental impacts. Herein, an environmental study is conducted wherein life cycle assessment (LCA) is applied to a two-scenario process for Disperse blue 60 production with short and long processing chains with different (a) material types, (b) consumptions, (c) processes, and (d) functional units with yields of 300 t/a. The most important influenced substances of the two scenarios were sodium cyanide and electricity next. Results proved that the largest damage of the dye production was attributed to resources and reached 46 and 62 kPt in the two scenarios. Compared with the conventional coal-fired power generation, damaged values of electricity from nature gas (NG) could reduce from 102 to 86 kPt in scenarios 1 and from 123 to 104 kPt in scenarios 2, respectively. When the electricity switched from NG to solar power, the values of the two scenarios could further decrease by 17 and 27 kPt, respectively. Therefore, the process of scenario 1 with the short process chain was more environmentally friendly for the production of Disperse blue 60 owing to the more efficient process and lower resource consumption. Graphic abstract.

Enhancement of Oxidation Efficiency of Elemental Mercury by CeO2/TiO2 at Low Temperatures Governed by Different Mechanisms.

This study aims to investigate the photothermal oxidation removal of Hg0 in simulated flue gases using photothermal catalysts at relatively low temperatures of 120-160 °C in two phases: the first phase applied the sol-gel method to prepare TiO2 and CeO2/TiO2 photothermal catalysts and characterized surface properties by specific surface area analysis, X-ray diffraction, X-ray photoelectron spectroscopy (XPS), and photoluminescence spectroscopy. The second phase investigated the effects of operating parameters on Hg0 oxidation efficiency at lower temperatures of 100-160 °C. The operating parameters included reaction temperatures and modified concentrations of CeO2. Experimental results indicated that TiO2 prepared by the sol-gel method was mainly in the anatase phase. XPS analysis showed that Ce mostly existed in the form of Ce4+. The content of surface-chemisorbed oxygen increased with the modification amount of CeO2. Photothermal catalytic oxidation results indicated that CeO2/TiO2 had a much higher oxidation efficiency of Hg0 at 120-160 °C than neat TiO2, which increased from 30-60 to >90%. 7%CeO2/TiO2 not only had the best photothermal performance but also maintained high efficiency at a relatively higher reaction temperature of 160 °C.

Alkali-Poisoning-Resistant Fe2O3/MoO3/TiO2 Catalyst for the Selective Reduction of NO by NH3: The Role of the MoO3 Safety Buffer in Protecting Surface Active Sites.

The exhaust gas contains harmful products, including fuel-additive elements such as compounds of sodium, which cause dramatic catalyst deactivation of catalysts during selective catalytic reduction (SCR) of NO with NH3. There is an increasing demand to synthesize alkali-poisoning-resistant catalysts for industrial NH3-SCR applications. In this study, the as-synthesized Fe2O3/MoO3/TiO2 exhibits a high degree of resistance toward Na2SO4 poisoning during the NH3-SCR reaction. With 500 µmol g-1 Na+ poisoning, Fe2O3/MoO3/TiO2 showed approximately 95% (or more) of its original activity throughout the entire temperature rage. Even with 700 µmol g-1 Na+ poisoning, Fe2O3/MoO3/TiO2 still performed well. The 500 and 700 µmol g-1 Na+ loadings dictate that, on average, SCR catalysts could be exposed to alkali-rich and highly dusty environments for more than 14 000 and 20 000 h, respectively. The layered MoO3 building block is used as a binding buffer and sandwiched between the active phase and TiO2 support to provide sufficiently stable binding sites for Na2SO4 poison and to present alkali blocking of the surface active phase. Our findings provide useful information regarding the use of MoO3 as a safety buffer for developing functional NH3-SCR catalysts with enhanced alkali-poisoning-resistant performance and long lifetimes.

Chemical fingerprint and source apportionment of PM2.5 in highly polluted events of southern Taiwan.

To investigate the spatial distribution and diurnal variation of the chemical composition of PM2.5 pollution in an industrial city of southern Taiwan, 12-h PM2.5 was diurnally continuously collected simultaneously at the Kaoping Air Quality Zone (KAQZ) during one highly PM2.5-polluted episode. Water-soluble ions, metallic elements, carbonaceous contents, dicarboxylic acids, and anhydrosugars were analyzed to characterize the chemical fingerprint of PM2.5. Backward trajectory simulation and chemical mass balance (CMB) receptor modeling were applied to identify the potential sources of PM2.5 and their contributions. It showed that Chaozhou (rural area) accompanying the highest SORs and NORs suffered from the most severe PM2.5 pollution during the episode. Sulfate (SO42-) was probably formed by the atmospheric chemical reaction in the daytime, while NO3- processed at nighttime at the KAQZ. A homogeneous formation of NO3- occurred at Chaozhou. The concentrations of Zn, Pb, Fe, Cu, V, and Al, mainly emitted from anthropogenic sources, increased significantly at the KAQZ. The highest OC, SOC/OC, and DA/OCs at Daliao (industrial area) were attributed to the transformation of primary VOCs to secondary OC via photo-oxidation during the episode. Oxalic acid was mainly produced through photochemical reactions since a high correlation between oxalic acid and Ca2+ was observed at Nanzi (urban area) and Daliao during the episode. During the episode, PM2.5 mostly originated from local primary or secondary aerosol than long-range overseas transport. The dominant source was anthropogenic emissions, accounting for 67.1% and 70.4% of PM2.5 at Nanzi and Daliao, respectively. At Chaozhou, the contribution of anthropogenic emissions was the lowest (42.4%), but secondary aerosols had the highest contribution of 38.3% of PM2.5 among the three areas during the episode.

Chemical characteristics, sources, and formation mechanisms of PM2.5 before and during the Spring Festival in a coastal city in Southeast China.

Severe pollution caused by atmospheric particulate matter (PM) has become a global environmental issue. Samples of atmospheric PM were collected before and during the Chinese Spring Festival in Xiamen, a coastal city in Southeast China, to investigate their chemical characteristics, sources, and formation mechanisms. The results indicated that PM2.5 mass concentrations comprised 53.60% and 56.31% of total suspended particulates before and during the Spring Festival, respectively. Due to the halt of factory production and construction and the reduction of vehicle flow during the Spring Festival, the concentrations of organic carbon, elemental carbon and water soluble ions in PM2.5 decreased by 78.56%, 84.19% and 27.53%, respectively, compared with those before the Spring Festival. However, the concentrations of K+, Mg2+, Al, Sr, and Ba increased by 3121.76%, 571.67%, 183.71%, 180.15%, and 137.58%, respectively, resulting from the display of fireworks and firecrackers during the Spring Festival. Analysis of backward air mass trajectory indicated that the concentrations of PM2.5 and its components were dominated by local pollution sources before and during the Spring Festival. The relationships between meteorological conditions and pollutant concentrations showed that the secondary organic aerosol was generated from the heterogeneous reaction before the Spring Festival, and the secondary inorganic aerosol was formed by the photochemical reaction during the Spring Festival.

Exceptional Activity over the Submonolayer MoO3 Motif on TiO2 for Nitrogen Oxide Emission Abatement.

Surface restructuring is a useful approach to modulating the properties of nanoparticles. A low-dimensional atomic-thickness active species may exhibit remarkably enhanced activity, in contrast to the inert nature of its bulk counterparts. Here, we report a procedure for growing in situ a low-dimensional monolayer-thick MoO3 entity from its bulk precursor. Traditional analysis of NO abatement catalyzed by vanadium-based materials implicates vanadium as the active site enhanced by the promoter element W or Mo. However, we report here that the atomic-thickness MoO3 film can function alone as an efficient NO abatement catalyst by itself; to achieve comparable performance with the industrial catalysts, it is not necessary to add vanadium oxide, which often has serious toxicity issues associated with it. We find that submonolayer MoO3 is responsible for the observed high activity. Electron microscopy and Raman spectroscopy reveal that the monolayer-thick MoO3 surface phase is directly attached to the anatase TiO2 support. The ab initio quantum calculations predict that the bidimensional MoO3 surface phase would provide more electron back-donation to the antibonding orbital of reactants and thus more efficient reactant activation. The spectral evolution of in situ DRIFTS indicates that the redox mechanism over the low-dimensional MoO3/TiO2 involves both Brønsted and Lewis acid sites during the reaction cycle.

Chemisorption and kinetic mechanisms of elemental mercury on immobilized V2O5/TiO2 at low temperatures.

To investigate the effect of low temperature and catalyst filling pattern on the adsorption of Hg° by DeNOx equipment, the chemisorption and kinetic mechanisms of Hg° adsorption on 5-30%V2O5/TiO2 immobilized on glass beads at 100-160 °C were investigated. The effects of the reaction temperature, influent Hg° concentration, and V2O5 doping amount on the adsorption efficiency and capacity for Hg° were explored. The active sites for Hg° adsorption were further identified. Additionally, the adsorption kinetics were modelled using the linear driving force approximation, Fick's diffusion model, and pseudo-second-order kinetic model. Finally, the influence of immobilization on the adsorption of Hg° was also investigated. Experimental results showed that the bridged oxygen atom of V-O-V played a key role in the adsorption of Hg°. The Hg° adsorption efficiencies decreased from >90% to 40% as the reaction temperature increased from 120 °C to 160 °C for 20%V2O5/TiO2, while the adsorptive capacities for Hg° were highly influenced by the influent Hg° concentration and V2O5 doping amount. 20%V2O5/TiO2 had the highest adsorptive capacity of 2547 µg Hg°/g V2O5/TiO2 at 160 °C. The kinetic results showed that the linear driving force approximation model fit the Hg° adsorption better than the other models. The diffusion resistance increased significantly for the immobilized catalysts because the external mass transfer coefficient decreased by more than 1200-fold.

Metallic characteristics of PM2.5 and PM2.5-10 for clustered Aeolian Dust Episodes occurred in an extensive fluvial basin during rainy season.

Aeolian dust episodes (ADEs) have been an emergency disaster in the Kaoping River Valley during the rainy season (May-September), which can severely deteriorate ambient particulate air quality in the region surrounding the Kaoping River. Thus, this study aims to characterize the metallic fingerprint of Aeolian dust (AD) and investigate the effects of ADEs on ambient particulate air quality along the Kaoping River Valley. Four manual sampling sites adjacent to the riverside were selected to collect fine (PM2.5) and coarse (PM2.5-10) aerosol samples during and after the ADEs in the periods of six events. A total of 13 metallic elements were analyzed using an inductively coupled plasma-atomic emission spectrometer. With metallic elements analysis and nonparametric statistical methods of Wilcoxon rank-sum test and Kruskal-Wallis test, this study successfully derived the metallic indicators of ADEs. The mass ratios of crustal elements (Fe, Ca, or Al) to reference element (Cd) obtained during the ADEs were much higher than those obtained after the ADEs. High mass ratios of Fe/Cd, Ca/Cd, and Al/Cd in PM2.5-10 were observed on the influenced areas of ADEs. Among them, (Fe/Cd)2.5-10 was proven as the best indicator which can be applied to effectively validate the existence of ADEs and evaluate their influences on ambient air quality. Moreover, PM2.5 concentrations during the ADEs were 3-3.6 fold higher than those after the ADEs. PM2.5 should be a contributor to AD, even though the mass ratios of PM2.5/PM10 ranged from 0.05 to 0.20 during the ADEs. Our findings provide valuable information regarding the characteristics of the AD during the ADEs in the Kaoping River. IMPLICATIONS: Indicators of (Fe/Cd)2.5-10 are approximately applied to observe the effects of ADEs. Local governments could realize the mechanisms of S- and NW-type aeolian dust episodes (ADEs). They can cause deterioration in different ways for the regional air quality surrounding Kaoping River Valley. Residents who have been living in the influenced areas can take precautions to prevent damage from aeolian dust. Strategies for curbing ADEs must reduce the area of bare lands by artificial measures in the long period of the sunny days during the rainy season. Future research should examine physical conditions of topsoils and other chemical composition in aeolian dust.

How incense and joss paper burning during the worship activities influences ambient mercury concentrations in indoor and outdoor environments of an Asian temple?

This study firstly investigated the species, concentration variation, and emission factors of mercury emitted from the burning of incenses and joss papers in an Asian temple. Both indoor and outdoor speciated mercury (GEM, GOM, and PHg) were sampled by manual samplers, while ambient GEM at an indoor site was in-situ monitored by a continuous GEM monitor. Field measurement results showed that the total atmospheric mercury (TAM) concentrations in indoor and outdoor environments were in the range of 8.03-35.72 and 6.03-31.35 ng/m3, respectively. The indoor and outdoor ratios (I/O) of TAM in the daytime and at nighttime were in the range of 0.64-0.90 and 1.50-2.04, respectively. The concentrations of GEM, GOM, and PHg during the holiday periods were approximately 1-4 times higher than those during the non-holiday periods. GEM was the dominant mercury species in the indoor and outdoor environments and accounted for 63-81% of TAM, while the oxidized mercury accounted for 19-37% of TAM. Burning incenses and joss papers in a combustion chamber showed that the concentration of GEM from joss paper burning ranged from 4.07 to 11.62 µg/m3, or about 13.97 times higher than that of incense burning, while the concentration of PHg from incense burning ranged from 95.91 to 135.07 ng/m3, or about 3.29 times higher than that of joss paper burning. The emission factors of incense burning were 10.39 ng/g of GEM and 1.40 ng/g of PHg, while those of joss paper burning were 12.65 ng/g of GEM and 1.27 ng/g of PHg, respectively. This study revealed that speciated mercury emitted from worship activities had significant influence on the indoor and outdoor mercury concentrations in an Asian temple. Higher intensity of worship activities during holidays resulted in a higher concentration of speciated mercury in indoor and outdoor air, which might cause health threats to worshipers, staffs, and surrounding inhabitants through long-term exposure.

Removal of elemental mercury by TiO2doped with WO3 and V2O5 for their photo- and thermo-catalytic removal mechanisms.

The catalytic removal of Hg(0) was investigated to ascertain whether the catalysts could simultaneously possess both thermo- and photo-catalytic reactivity. The immobilized V2O5/TiO2 and WO3/TiO2 catalysts were synthesized by sol-gel method and then coated on the surface of glass beads for catalytic removal of Hg(0). They were also characterized by SEM, BET, XRD, UV-visible, and XPS analysis, and their catalytic reactivity was tested under 100-160 °C under the near-UV irradiation. The results indicated that V2O5/TiO2 solely possessed the thermo-catalytic reactivity while WO3/TiO2 only had photo-catalytic reactivity. Although the synthesis catalytic reactivity has not been found for these catalysts up to date, but compared with TiO2, the removal efficiencies of Hg(0) at 140 and 160 °C were enhanced; particularly, the efficiency was improved from 20 % at 160 °C by TiO2 to nearly 90 % by WO3/TiO2 under the same operating conditions. The effects of doping amount of V2O5 and WO3 were also investigated, and the results showed that 10 % V2O5 and 5 % WO3/TiO2 were the best immobilized catalysts for thermo- and photo-catalytic reactivity, respectively. The effect of different influent concentrations of Hg(0) was demonstrated that the highest concentration of Hg(0) led to the best removal efficiencies for V2O5/TiO2 and WO3/TiO2 at 140 and 160 °C, because high Hg(0) concentration increased the mass transfer rate of Hg(0) toward the surface of catalysts and drove the reaction to proceed. At last, the effect of single gas component on the removal of Hg(0) was also investigated.

Enhanced photocatalytic oxidation of gaseous elemental mercury by TiO2 in a high temperature environment.

The photo-oxidation of Hg(0) in a lab-scale reactor by titanium dioxide (TiO2) coated on the surface of glass beads was investigated at high temperatures. TiO2 was calcinated at four different temperatures of 300 °C, 400 °C, 500 °C and 600 °C (noted as Ti300, Ti400, Ti500 and Ti600) and characterized for its physicochemical properties. The calcinated TiO2 coating on the glass beads was then tested to compare the photo-oxidation efficiencies of Hg(0) with an incident light of 365 nm. The results showed that the oxidation efficiencies of Hg(0) for Ti400 and Ti500 were higher than those of Ti300 and Ti600. To enhance the photo-oxidation efficiency of Hg(0), Ti400 was selected to examine the wave lengths (λ) of 254 nm, 365 nm and visible light with various influent Hg(0) concentrations. The effects of irradiation strength and the presence of oxygen on the photo-oxidation efficiency of Hg(0) were further investigated, respectively. This study revealed that the wave length (λ) of 254 nm could promote the photo-oxidation efficiency of Hg(0) at 140 and 160 °C, while increasing the influent Hg(0) concentration and could enhance the photo-oxidation rate of Hg(0). However, the influence of 5% O2 present in the flue gas for the enhancement of Hg(0) oxidation was limited. Moreover, the intensity of the incident wave length of 365 nm and visible light were demonstrated to boost the photo-oxidation efficiency of Hg(0) effectively.