Activity For Combustion Research Articles

Effects of chemical composition of ambient PM2.5 measured in Seoul on potential health risks and generation of reactive oxygen species

This study assesses the health effects associated with the chemical species of ambient particulate matter (PM) with an aerodynamic diameter ≤2.5 μm (PM2.5) in Seoul, focusing on identifying key chemical constituents and their sources. We employed two approaches to estimate health risks: (1) evaluating carcinogenic and noncarcinogenic risks using IRIS (Integrated Risk Information System) data from the US EPA (Environmental Protection Agency), and (2) quantifying the generation of hydroxyl radicals (·OH) following exposure to PM2.5 in surrogate lung fluid (SLF). Our results show a significant impact on human health from certain elements (Cr, Ni, As, and Cd) and polycyclic aromatic hydrocarbons (PAHs) (DaeP, DahA, and BaP for carcinogenic risks; BaP and BeP for noncarcinogenic risks). Notably, Cr and BaP, which are influential in both risk assessment and ·OH generation, highlight their significant roles in human health impacts. However, other components (e.g., CPP, BaP, BghiP, BaA, CHR, PYR, FLT, Ca, Mg, and Cu), though contributors to ·OH generation, were not included in the EPA's health risk assessment, suggesting a need for a broader PM2.5 compositional analysis to more accurately determine exposure concentrations and assess inhalation risks. These components predominantly originate from anthropogenic sources, such as combustion, vehicles, and industrial activities, underscoring the significant health implications of the pollutants emitted from these sources. The study concluded that focusing solely on the mass reduction of PM2.5 may not suffice; a dual approach that reduces both mass concentration and chemical-specific health risks is imperative for effective public health protection.

Comprehensive analysis of air pollution and the influence of meteorological factors: a case study of adiyaman province.

Adıyaman, a city recently affected by an earthquake, is facing significant air pollution challenges due to both anthropogenic activities and natural events. The sources of air pollution have been investigated using meteorological variables. Elevated southerly winds, especially prominent in spring and autumn, significantly contribute to dust transport, leading to a decline in local air quality as detected by the HYSPLIT model. Furthermore, using Suomi-NPP Thermal Anomaly satellite product, it is detected and analyzed for crop burning activities. Agricultural practices, including stubble burning, contribute to the exacerbation of PM10 pollution during the summer months, particularly when coupled with winds from all directions except the north. In fall and winter months, heating is identified as the primary cause of pollution. The city center located north of the station is the dominant source of pollution throughout all seasons. The study established the connection between air pollutants and meteorological variables. Furthermore, the Spearman correlation coefficients reveal associations between PM10 and SO2, indicating moderate positive correlations under pressure conditions (r = 0.35, 0.52). Conversely, a negative correlation is observed with windspeed (r = -0.35, -0.50), and temperature also exhibits a negative correlation (r = -0.39, -0.54). During atmospheric conditions with high pressure, PM10 and SO2 concentrations are respectively 41.2% and 117.2% higher. Furthermore, pollutant concentration levels are 29.2% and 53.3% higher on days with low winds. Last, practical strategies for mitigating air pollution have been thoroughly discussed and proposed. It is imperative that decision-makers engaged in city planning and renovation give careful consideration to the profound impact of air pollution on both public health and the environment, particularly in the aftermath of a recent major earthquake.

Magnesium borate whiskers/La2-XCeXZr2O7 catalysts preparation on cordierite honeycomb ceramic surfaces for soot catalytic oxidation͏

Magnesium borate whiskers were used to prepare a hierarchical microstructure on cordierite ceramic substrate through the precipitation-molten salt method. The La2-XCeXZr2O7 catalyst was then loaded onto the magnesium borate whiskers to form the hierarchical microstructure. The Ce-doped catalysts exhibited a significant improvement in the catalytic activity of soot combustion compared to the La2Zr2O7 catalyst. The study employed various techniques to characterize the structural morphology and phase composition, including scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), Fourier transform-infrared spectroscopy (FT-IR), and X-ray diffraction (XRD). The growth of Magnesium borate whiskers (Mg2B2O5) with diameters of 100–200 nm and lengths of 2–5 μm were grown and tightly bonded to the cordierite ceramic substrate to mimic the structure of human respiratory system cilia. This could improve the filtration efficiency of soot in car exhaust. BET analysis showed that the specific surface area of cordierite increased from 0.684 m2/g to 1.363 m2/g after whisker growth. The study confirmed that the whiskers were firmly attached to the cordierite ceramic substrate, as demonstrated by the binding strength experiments. The addition of Ce metal has been found to significantly enhance soot combustion due to the presence of more active oxygen species and superior mobility of lattice oxygen species with more oxygen vacancies. The catalyst's intrinsic redox property was characterized using X-ray photoelectron spectroscopy (XPS) and H2 temperature-programmed reduction (H2-TPR). The semi-quantitative thermogravimetric analysis (TG-DTG) and the temperature-programmed oxidation (TPO) of catalysts showed that Z-La1.9Ce0·1Zr2O7 exhibited the highest catalytic activity for soot combustion, with an ignition temperature of 268 °C, a peak temperature of 418 °C, and a temperature of 90 % soot conversion of 464 °C. Furthermore, cyclic stability experiments demonstrate that the Z-La1.9Ce0·1Zr2O7 catalyst exhibits excellent structural stability and consistent catalytic performance. This distinctive microstructure holds great potential for applications in the field of DPF.

Redox-driven surface generation of highly active Pd/PdO interface boosting low-temperature methane combustion

The supported Pd catalyst has been a benchmark for methane elimination. However, the active structures have been long under debate. Here, by the aberration-corrected high angle annular dark field scanning transmission electron microscopy, operando X-ray absorption spectroscopy and quasi in situ X-ray photoelectron spectroscopy, we revealed the two-dimensional metallic Pd bumps on the PdO surface (litchi-like structure) generated by the redox atmosphere under the lean condition as a highly active structure of the Pd/Al2O3 catalyst. The substantially increased Pd/PdO interfaces boost the methane combustion activity higher than the similar catalysts reported previously, and remarkably enhance the reaction rate by 15.5 and 10.7 times that of pure PdO or metallic Pd counterpart under lean condition at 300 °C, respectively. Density-functional theory calculations confirm the synergistic C–C bond activation of methane on the Pd/PdO interfaces. Our work provides new insight into the traditional understanding of the chemical state and particle size effects of the industrial Pd catalysts for methane oxidation.

Impact of terephthalic acid emissions from intensive nocturnal biomass incineration on oxidative potential in Seoul, South Korea

This study investigated the impact of large-scale incineration facilities on PM2.5 levels in Seoul during winter. Due to the challenge of obtaining accurate combustion data from external sources, heat supply records were used as a proxy for combustion activity. To assess health risks, dithiothreitol-oxidative potential (DTT-OP) was analyzed to identify potential hazards to human health. By comparing DTT-OP with PM2.5 sources related to combustion, the study aimed to understand the impact of local pollution sources on human health in Seoul. The diurnal analysis showed that oxidative potential (0.19 μM/m3) and the biomass burning factor (5.53 μg/m3) peaked between 4:00 and 8:00 AM, with lower levels observed from 12:00 to 20:00. A significant correlation was found between combustion sources and oxidative potential, with a high correlation coefficient (r2 = 0.92). The presence of terephthalic acid (TPA) in the Cellulose combustion source profile, which is produced by the pyrolysis of plastics like polyester fiber and polyethylene terephthalate (PET), further supported the link to emissions from incineration facilities. These findings suggest that the biomass burning source is strongly correlated with DTT-OP, indicating a significant association with health risks among various local sources of PM2.5 in Seoul.

Potential for low-emissions oil palm production in Indonesia: insights from spatiotemporal dynamics

Rising global demand for palm oil has created environmental pressures related to deforestation, burning, and peat exploitation, which in turn drives increased greenhouse gas (GHG) emissions. GHG emissions in oil palm (OP) production are known to vary spatially. However, temporal changes across contrasting management and soil types, are less well studied. This paper quantifies spatiotemporal GHG emissions across contrasting regions, management types, and soil types for the period 1990–2019 to assess the potential for reducing emission. The study focusses on Indonesia, as the biggest producer of OP, and in particular on the North Sumatra and Riau provinces, where OP is intensively produced. GHG inventories in 5 year time steps were constructed to investigate the change in drivers of emissions using spatial data, resampled to a 500 m grid. Total GHG emissions were found to have increased in both regions due to expanding OP production. However, results show a reduction in emissions flux from 1.98 to 1.15 Ton Ceq. ha−1yr−1 in North Sumatra and 9.63–2.67 Ton Ceq. ha−1yr−1 in Riau over the study period. This reduced flux was linked to the decreased deforestation and burning activities, together with increased biomass increment from lower carbon stock area conversion to OP. In both provinces, smallholder plantations emitted fewer emissions than industrial ones, and production on organic soils resulted in consistently higher emissions than on mineral soils. In North Sumatra, emissions under all management and soil types were found to decrease. In Riau, however, GHG emissions on organic soils regardless of management types, remained high. Our findings emphasise that potential for low-emissions OP production is attainable by reducing emissions per unit area through an improved understanding of GHG emissions spatiotemporal variability and their drivers. These contribute to reinforcing ongoing government regulations and guiding the industry towards low-emission OP productions.

Regulating the synergy of sulfate and Pt species in Pt/ZSM-5 for propane complete oxidation

Modulating the active sites in atomic level is very meaningful to optimize catalyst performance but still very challenge. Herein, Pt catalysts loaded on different supports (ZSM-5, Al2O3, ZrO2, CeO2) were sulfate modified by in situ pyrolysis of (NH4)2SO4 mixed with Pt catalyst. Sulfate remarkably improves these catalyst activities for propane combustion, particularly for the sulfate modified Pt/ZSM-5 catalyst with the highest activity among them. Through controlling the amount of (NH4)2SO4 used and the loading of Pt, Pt/S atomic ratio in the sulfate modified Pt/ZSM-5 catalyst was successfully regulated. Pt/S atomic ratio significantly affects the electron transfer from Pt species to sulfate and also their interaction strength, which is decisive to the synergetic catalysis of sulfate and Pt species. The 5S-2Pt/ZSM-5 with Pt/S atomic ratio of 0.5 shows a moderate strength of sulfate and Pt species interaction, which is responsible for its highest reaction rate of 86.5 μmol·gPt−1·s−1 at 200 °C.

Promoting effect and kinetic analysis of Fe-Co bimetallic doping on the LaMnO3 catalytic activity for methane combustion

To enhance the catalyst’s properties, a modified sol–gel method is developed in this study, and a unique perovskite catalyst, LaMnxFeyCo1-x-yO3, is successfully synthesized by doping Fe-Co into the lattice of LaMnO3. The catalytic activity of the synthesized catalysts is initially determined by applying them to methane oxidation. Then, the structural, chemical, and surface properties of these catalysts are systematically evaluated utilizing XRD, BET, O2-TPD, H2-TPR, SEM, and XPS analyses. The modified LaMn0.8Fe0.15Co0.05O3 is shown to exhibit excellent activity (T90 at 486.5 ℃) in methane catalytic combustion, comparable to several standard noble metal materials. Experimental findings indicate that such perovskite structures have a larger specific surface area, an elevated molar ratio of Mn4+, desirable low-temperature reducibility, and excellent oxygen mobility relative to the original LaMnO3. Meanwhile, more efficient electron transfer from Mn4+/Mn3+ redox cycles, as well as the emergence of oxygen defects, significantly contribute to the robust interaction between Fe-Co and LaMnO3. Further reaction kinetic analysis is conducted to determine changes in species components and identify possible catalytic pathways. Notably, Fe-Co co-doping leads to an improvement in the increase of lattice oxygen and CH4 adsorption. In addition, the MVK kinetic mechanism governs methane combustion over LaMn0.8Fe0.15Co0.05O3. This study provides new insights into enhancing energy conversion performance and efficient utilization of ventilation air methane (VAM) through the implementation of highly efficient perovskites.

Facile construction and enhanced catalytic activity of Co-Mn oxide with rich amorphous/crystalline interfaces for propane oxidation

Cobalt-manganese (Co-Mn) composite oxides show high potential for the catalytic oxidation of volatile organic compounds (VOCs). However, the low defect content and poor oxygen mobility of perfect spinel structure crystalline always make it difficult to effectively activate C–H bonds of propane. Here, the catalyst with rich amorphous MnOx/crystalline Co3O4 interfaces was prepared, and the catalytic combustion activity for propane was determined. The rich amorphous/crystalline interfaces CMO-400 (i.e. Co-Mn oxide calcined at 400 °C) catalyst exhibited the best catalytic activity for propane with T90 of 200 °C among all bimetallic Co-Mn oxides. Various characterizations and corresponding results have demonstrated that the abundant amorphous/crystalline interfaces could improve the catalytic performances, attributed to high oxygen vacancy concentration, low temperature reducibility, weak Mn−O bond strength, and good surface lattice oxygen mobility. It is noteworthy that the interface engineering of amorphous/crystalline is an effective strategy in VOCs catalytic oxidation.

Optimization of CO2/N2 injection ratios in goaf by saturation adsorption capacity

The inerting technology is a common means to prevent fires in goaf of coal mine, in which adsorption capacity is the key index to measure the inerting effect. Therefore, this paper obtained the coal spontaneous combustion (CSC) stage of Qianyingzi coal mine through programmed heating experiments, and determined the physical adsorption stage temperature (below 323.15 K) matching the actual environment. The oxidation characteristics of coal samples with different adsorption degrees were further studied by adsorption experiment and TG-DSC test. The results indicate that the combustion activation energy of coal samples follows the sequence of second-stage adsorption coal > dried coal > raw coal > first-stage adsorption coal. This implies that the CO2 saturated adsorption can exert a specific inhibitory impact on coal combustion. Therefore, the index of the saturation adsorption capacity (SAC) was proposed to evaluate the inerting effect. We further studied the adsorption capacity of coal at different ratios of CO2/N2 by molecular simulation under different pressures (0–5 MPa). The results show that CO2 dominates in both single-component adsorption and competitive saturated adsorption. The average of ratios (AOR) and average of differences (AOD) threshold are determined. The priority of SAC is obtained in the order of single-component (CS), CO2/N2 mixture ratio at 4:6 (C4:6), CO2/N2 mixture ratio at 2:8 (C2:8) from largest to smallest. Furthermore, a fuzzy optimization method for injection ratio of CO2/N2 under different pressures was established. During dynamic changes in environmental pressure, it is appropriate to inject CO2 separately at 0.2–2.5 MPa. At 3 MPa, a mixture of CO2/N2 at a ratio of 2:8 is the best for prevent fires in goaf. Similarly, an inert gas with a CO2/N2 ratio of 4:6 is injected at 3–5 MPa.

Co3O4-Based Materials as Potential Catalysts for Methane Detection in Catalytic Gas Sensors.

The present work deals with the development of Co3O4-based catalysts for potential application in catalytic gas sensors for methane (CH4) detection. Among the transition-metal oxide catalysts, Co3O4 exhibits the highest activity in catalytic combustion. Doping Co3O4 with another metal can further improve its catalytic performance. Despite their promising properties, Co3O4 materials have rarely been tested for use in catalytic gas sensors. In our study, the influence of catalyst morphology and Ni doping on the catalytic activity and thermal stability of Co3O4-based catalysts was analyzed by differential calorimetry by measuring the thermal response to 1% CH4. The morphology of two Co3O4 catalysts and two NixCo3-xO4 with a Ni:Co molar ratio of 1:2 and 1:5 was studied using scanning transmission electron microscopy and energy dispersive X-ray analysis. The catalysts were synthesized by (co)precipitation with KOH solution. The investigations showed that Ni doping can improve the catalytic activity of Co3O4 catalysts. The thermal response of Ni-doped catalysts was increased by more than 20% at 400 °C and 450 °C compared to one of the studied Co3O4 oxides. However, the thermal response of the other Co3O4 was even higher than that of NixCo3-xO4 catalysts (8% at 400 °C). Furthermore, the modification of Co3O4 with Ni simultaneously brings stability problems at higher operating temperatures (≥400 °C) due to the observed inhomogeneous Ni distribution in the structure of NixCo3-xO4. In particular, the NixCo3-xO4 with high Ni content (Ni:Co ratio 1:2) showed apparent NiO separation and thus a strong decrease in thermal response of 8% after 24 h of heat treatment at 400 °C. The reaction of the Co3O4 catalysts remained quite stable. Therefore, controlling the structure and morphology of Co3O4 achieved more promising results, demonstrating its applicability as a catalyst for gas sensing.

Characteristics of Atmospheric Pollutants in Paddy and Dry Field Regions: Analyzing the Oxidative Potential of Biomass Burning

This study aimed to identify the characteristics of atmospheric pollutants emitted by agricultural activities and to evaluate factors that may cause harm to human health. For the research, atmospheric pollutants were measured over the course of a year in representative rice farming and field crop farming areas in South Korea. The results confirmed that the characteristics of atmospheric pollutants in agricultural areas are influenced by the nature of agricultural activities. Specifically, when comparing rice paddies and field crop areas, during summer, the correlation between oxidative potential and levoglucosan—a marker for biomass burning—weakens due to less burning activity in the rice-growing season, leading to lower oxidative potential despite different PM2.5 across areas. The study also finds that methyl sulfonic acid, indicating marine influence, plays a big role in keeping oxidative potential low in summer. This suggests that the main causes of PM2.5-related health risks in the area are from biomass burning and external sources, with burning being a significant factor in increasing oxidative potential. Based on these results, it is hoped that measures can be taken in the future to reduce atmospheric pollutants in agricultural areas.

Research on the co-combustion characteristics and kinetics of rice husk hydrochar with anthracite

Co-combustion of anthracite and hydrochar derived from hydrothermal carbonization with process water recirculation was proposed as an effective way to achieve a transition to low-carbon energy in industries that rely heavily on coal combustion. In this study, thermogravimetric analysis and model-free methods were employed to investigate the co-combustion characteristics and kinetics of anthracite and hydrochar. The results demonstrate that the carbon content of hydrochar is lower than that of anthracite, but the volatile content is higher than that of anthracite, indicating that hydrochar has better combustion performance. There is a synergistic effect in the co-combustion reaction of hydrochar and anthracite. With the increase of the hydrochar addition ratio, the ignition and burnout temperatures of anthracite decrease gradually. With the increase of temperature rise rate, the combustion reaction is enhanced and the combustion performance of anthracite is improved under the fixed mixing ratio. According to the calculation of combustion activation energy by Flynn-Wall-Ozawa and Kissenger-Akahira-Sunose methods, the apparent activation energy of the mixed samples gradually decreases with the increase of combustion conversion rate. When the addition of hydrochar is 60 %, the average apparent activation energy of the mixed sample is the lowest, which is 66.51 kJ mol−1 and 54.62 kJ mol−1, respectively.

In-situ reconstruction of LaCoO3-Co3O4 hetero-interface over lanthanum modified Co3O4 nanocatalyst for improved catalytic activity and sintering resistance in methane combustion

Nanoparticles-based catalysts still suffer from deactivation due to sintering and structural collapse through long-time running at high reaction temperature. Developing simple strategy for improving the sintering resistance of nanoparticles is of great importance for fabrication of durable heterogeneous catalysts. In this work, lanthanum was used to prevent Co3O4 nanoparticles from sintering with restricting growth of nanocrystals by in-situ generation of LaCoO3 perovskite phase during thermal ageing process, further building LaCoO3-Co3O4 hetero-interface with strong interfacial effect. Specifically, the Co3O4 nanocatalyst was loaded with different amount of La by traditional impregnation method and a series of characterizations were carried out to explore the physical and chemical properties of the as-prepared catalysts, including XRD, Raman, BET, SEM, HRTEM, XPS, H2-TPR and O2-TPD. It was found that 5 wt% La-Co3O4 has the highest catalytic activity in CH4 combustion and the value of T90 (temperature of 90% methane conversion) between fresh and aged was only 9 ºC, while this value was 108 ºC over pure Co3O4 sample. The Raman, XPS, H2-TPR and O2-TPD results exhibited that the synergistic effect between Co3O4 and LaCoO3 could not only induce lattice distortion in Co3O4 with more defects and adsorbed oxygen species, enhanced oxygen mobility and reducibility, but also significantly suppress the growth of Co3O4 nanocrystals during thermal ageing treatment.

Decoding the Reactivity Enhancement of Ln2Ce2O7 Compounds (Ln = Yb, Y, Tb, and Gd) for Soot Combustion: The Remarkable Contribution of Variable Valence A-Sites.

The impact of variable valence A-sites on the redox property and reactivity of Ln2Ce2O7 compounds in soot particulate combustion has been investigated. It was observed that Yb2Ce2O7, Y2Ce2O7, and Gd2Ce2O7 formed a rare earth C-type phase, while Tb2Ce2O7 formed a solid solution phase. Both Tb2Ce2O7 and Yb2Ce2O7 possess dual valence state A-sites, resulting in significantly more surface vacancies. Additionally, the advantageous solid solution phase structure of Tb2Ce2O7 leads to even more surface vacancies than Yb2Ce2O7, which is crucial to generate active oxygen sites. Moreover, the introduction of NO into the reaction feed enhances combustion activity by producing active surface monodentate nitrates. A catalyst with higher numbers of surface vacancies exhibits improved NO oxidation ability and better NO2 utilization efficiency. Consequently, the Tb2Ce2O7 compound demonstrates not only the best soot combustion activity, but also an optimal NOx-assistance effect. Therefore, it is concluded that variable valence A-site is the intrinsic factor to improve the reactivity of Ln2Ce2O7 catalysts.

Experimental and theoretical investigation on the high activity La0.8-xSr0.2KxMn1-yByO3-δ perovskite catalyst with combined A and B site modifications

In this work, a series of LaMnO3 (LM) perovskite catalysts modified at A and B sites were prepared to accelerate soot combustion. The La0.68Sr0.2K0.12Mn0.9Cu0.1O3-δ (LSK0.12MCu0.1) modified by Sr, K and Cu has good catalytic activity and cycle stability, the presence of NO can obviously promote the oxidation of soot. A variety of characterization results show that doping the A and B sites of perovskite will not destroy the original structure of perovskite, and the doped ions (Sr2+, K+, and Cu2+) can enter the perovskite catalyst well, which may be conducive to the formation of more oxygen defects and active oxygen species. According to the DFT calculation, adding Sr and K to the A sites can alter how atoms interact in a perovskite catalyst, increase the amount of unsaturated coordination bonds, and encourage the development of high-valence active ions (Mn4+) and oxygen defects. The doping of transition metal to the B sites results in the formation of the Cu-O-Mn link, which forms the Mn(Cu)O6 octahedron and stimulates the development of oxygen vacancies and the release of active oxygen. This study will provide an important reference for developing non-precious metal-based perovskite materials with high activity and low cost for catalytic combustion.

Penerapan Pajak Karbon dalam Mewujudkan Sustainability Development Goals Serta Dampaknya Terhadap Penerimaan Pajak di Indonesia

Climate change is caused by the burning of fossil fuels that produce greenhouse gas emissions that can raise temperatures globally. The government is trying to control climate change, one of which is by setting targets for reducing greenhouse gas emissions and implementation a carbon tax. The implementation of carbon tax is change industrial behavior to switch green economy activites that are low in carbon emissions. The purpose of this research is to forecast the impact of carbon tax on potential state revenue to reduce the amount of carbon emissions in Indonesia to support the achievement of Sustanability Development Goals (SDGs). The method of the research used is qualitative method with content analysis approach using corbon emission data from Statistical Review Energy 2023 and scoping review approach from national and international literature such as working papers, scientific articles, etc obtained based on keyword for from search engine. Based on the scoping review step, 5 articles were obtained that can detail represented about the implementation of carbon tax can be reduce carbon emission to realize the Sustainability Development Goals (SDGs) in the Asia Pacific. The energy sector was chosen because the consumption has increased, energy sector is the largest contributed carbon dioxide consumption globally was compared to other sectors due to increased combustion activities of carbo containing compounds. Based on the result, implementation of carbon tax have applied by the government could be provide potential state revenue from the energy sector worth IDR23.280 trilion in 2025. The potential tax revenue generated from carbon tax ca be used to the impacts of climate change to support the achievement of Sustainability Development Goals (SDGs). The implementation of carbon tax is expected to change industry behaviour to green economic activities that are low in carbon emission leading to the achievement of the SDGs

Efficient catalytic combustion of propane at low temperature based on ignition effect caused by amorphous atomic-layer Pt clusters

Developing highly active catalysts for hydrocarbon combustion at low temperatures is paramount but yet challenging. The crystal form of carrier and the dispersion degree of active species have great influence on propane combustion catalysts, but its internal mechanism is still unclear. In this study, the amorphous atomic-layer Pt clusters (AL) and Pt single atoms (SA) on TiO2 with various crystal phases were prepared and used as propane combustion catalysts, where the as-synthesized Pt/a-TiO2 catalyst with atomic-layer Pt clusters exhibited better catalytic performance. The Pt/a-TiO2-AL could achieve a 90 % propane conversion (T90) at 230 °C, with the highest reaction rate (39.57 × 10−7 mol g−1 s−1) and TOF value (7.72 × 10−2 s−1) at 240 °C. Kinetic studies showed that oxygen had a lower inhibitory effect on Pt/a-TiO2-AL compared to that on the Pt/p-TiO2-AL and Pt/r-TiO2-AL catalysts; simultaneously, the Pt/a-TiO2-AL catalyst presented lower apparent activation energy compared with Pt/a-TiO2-SA. DFT results showed that atomic-layer Pt clusters on TiO2 had the lower formation energy of oxygen vacancy than Pt single atoms due to the synergistic effect between adjacent exposed Pt atoms in the fully exposed atomic-layer Pt clusters, which had a higher activation capacity for oxygen and thus accelerated propane combustion through the ignition effect (rapid activation of oxygen and rapid combustion of propane). Our primary results provide a promising approach for the creation of high-efficiency Pt-based catalysts, specifically tailored for the catalytic combustion of volatile organic compounds (VOCs).

Potential of Pinus eldarica Medw. tree bark for biomonitoring polycyclic aromatic hydrocarbons in ambient air

Urban trees' biomonitoring of pollutants such as polycyclic aromatic hydrocarbons (PAHs) yields pertinent and useful data for air pollution management. The aim of this study was to biomonitor PAHs in pine (Pinus eldarica Medw.) trees in the city of Isfahan and identify their sources. In total, 34 samples of outer bark of the trees were collected and their contents of 16 EPA PAHs were analyzed. With a median value of 136.3 ng/g, the total PAH contents in tree barks varied from 53.4 to 705.2 ng/g. The average values of the diagnostic ratios for Ant/(Ant + Phe), Flu/(Flu + Py), BaA/(BaA + Chr) and IP/(IP + BP) were 0.19, 0.49, 0.45 and 0.49, respectively, revealing the PAHs majority source of pyrogenic. Meanwhile, principal component analysis showed two major types of PAHs sources including pyrogenic (fossil fuel combustion and industrial activities) and petrogenic (uncombusted) sources. The average ratio An/(An + Phe) and Flu/(Flu + Py) in bark samples was close to their relevant ratios in ambient air which demonstrated the potential use of this approach for biomonitoring of PAHs.

Enhanced Ru-O-Ce interaction by solid solution structure of Ru-CexZr1-xO2 catalysts for efficient catalytic combustion of vinyl chloride

Ru-CexZr1-xO2 catalysts, prepared by stepwise precipitation method, were investigated for the catalytic combustion of vinyl chloride (VC). Ru-O-Ce is a highly reactive structure in the redox ability. The Ce-O-Zr solid solution structure enhances the strong metal-support-interaction (SMSI) between Ru and Ce, thereby increasing the content of Ru-O-Ce structure, which can be modulated by the molar ratio of Ce/(Ce + Zr) in the catalyst. Zr doping also enhances the surface acid sites. In situ DRIFTS reveals that Ru-CexZr1-xO2 catalyst avoids chlorine poisoning, and Ru-O-Ce provides sufficient chemically adsorbed oxygen species (CAOS) to promote formation of formate intermediate species. Ru-Ce0.5Zr0.5O2 catalyst exhibited the best catalytic performance with T90 of 227 °C under the reaction conditions of 1000 ppm VC and WHSV of 30,000 mL·g−1·h−1. Moreover, Ru-Ce0.5Zr0.5O2 catalyst exhibited the superior resistance to high temperature, chlorine poisoning and water, and excellent catalytic activity for the catalytic combustion of various VOCs.