Degradation Of Volatile Organic Compounds Research Articles

Active Interfacial Perimeter in Pt/CeO2 Catalysts with Embedding Structure for Water-Tolerant Toluene Combustion.

Supported Pt catalysts are often subjected to severe deactivation under the conditions of high temperature and water vapor in catalytic oxidation; thus, the superior stability and water-resistant ability of catalysts have great significance for the effective degradation of volatile organic compounds (VOCs). Herein, we constructed a Pt/CeO2-N catalyst with an active interfacial perimeter, in which Pt species were partially embedded in the defective CeO2-N support to prevent the sintering. A significant charge transfer between Pt species and ceria in the embedding structure occurred via the Pt-CeO2 interface, which induced the formation of a Pt4+-Ov-Ce3+ interfacial structure. Experimental research and theoretical calculations demonstrated that the active Pt4+-Ov-Ce3+ interface promoted the activation and migration of lattice oxygen, thus facilitating the participation of oxygen species in toluene oxidation. Consequently, Pt/CeO2-N showed excellent catalytic performance for toluene degradation. In situ DRIFTS and DFT calculation proved that the Pt4+-Ov-Ce3+ interfacial sites served as the intrinsic active center in the dissociation of H2O to generate ·OH, which contributed to the formation of benzaldehyde, thus remarkably improving the water-resistant property. This study provided a facile strategy for fabricating the interfacial embedding structure to enhance the catalytic activity and water tolerance for eliminating VOCs in practical application.

Microbial diversity and cover plants in de-sealed urban soil as strategies for mitigating anthropogenic volatile organic compounds

Urbanization exacerbates soil degradation, compromising global soil health and biodiversity. To reduce this, strategies for soil de-sealing and bioremediation are necessary. In a mesocosm experiment using a de-sealed soil from an urban site as substrate, an inoculum of arbuscular mycorrhizal fungi (AMF) and two cover plants, Cynara cardunculus L. and Trifolium repens L., were utilized to assess their effects on volatile organic compound (VOC) emissions and soil microbial community dynamics. The soil status was investigated employing soil VOC and metabarcoding analyses. Our results showed that the soil VOC emission was mainly composed by anthropogenic derived VOCs, especially arene and furan classes. These two classes were shown to be less concentrated in C. cardunculus soils, with and without AM fungal inoculation, suggesting a positive impact of these conditions on soil health restoration. Additionally, AM fungal inoculation of C. cardunculus resulted in increased bacterial alpha diversity, with enhanced Proteobacteria/Acidobacteria, Cyanobacteria/Chloroflexi, and Fungi/Bacteria ratios, suggesting an improvement in soil quality conditions. In our experimental conditions, order Chloroflexales and specific bacterial genera, including Ralstonia, Delftia, Ramlibacter, were identified as contributors to VOC degradation, highlighting their adaptability in contaminated environments. Overall, this study provided evidence on the importance of integrating AM fungal inoculation and specific flowerbed/ornamental plants in urban soil management after de-sealing processes.

Enhanced gaseous benzene degradation by bimetallic MIL-101(Fe, Cu) activated persulfate system: Efficiency and mechanism

Persulfate oxidation is a promising technology for air pollution control but still suffers from degrading refractory volatile organic compounds (VOCs) under mild conditions. Metal-doped metal-organic frameworks (MOFs) offer a novel strategy to enhance persulfate activation and VOCs degradation. Herein, a novel bimetallic MIL-101 (Fe, Cu) is prepared for more effective degradation of gaseous benzene via persulfate activation. Under optimal conditions (Fe/Cu ratio of 1:4, persulfate concentration of 7 mM/L, pH of 5, and reaction temperature of 70 °C), the MIL-101(Fe1, Cu4) activated persulfate system achieves a benzene degradation efficiency of 79.1 %, a value significantly higher than that of MIL-101(Fe) (20.1 %). The enhanced performance can be attributed to the synergistic effect of Fe²⁺/Fe³⁺ and Cu²⁺/Cu⁺ redox interactions facilitating the activation of persulfate and generation of radical species. Density functional theory (DFT) calculations indicate an increase in the adsorption energy of MIL-101(Fe) in the presence of Cu doping from −3.46 eV to −5.92 eV along with a rise in the Fermi energy level from 0.5 eV to 1.33 eV, enhancing the electron density and mobility. A reaction energy diagram is provided to illustrate the reaction pathways and transition states involved in the degradation of benzene. Overall, the incorporation of Cu in MOFs significantly enhances the efficiency of persulfate-based oxidation systems toward VOCs degradation.

Regulation of electron density in Pt nanoparticles via bimetallic metal-organic frameworks for enhancing photothermal catalysis of toluene decomposition

Volatile Organic Compounds (VOCs) are omnipresent in the sphere of human industrial, harboring latent adverse consequences for health and the ecological system. The photothermal catalytic oxidation of VOCs is an advanced integrated technology that harnesses the combined effects of light and heat energy to enhance the efficiency of VOCs degradation. Herein, a bimetallic Metal-Organic Framework (MOF) was synthesized with the incorporation of Ce into the UiO-66-NH2(Zr) (i.e., UNH(Zr)), UiO-66-NH2(Zr2Ce) (i.e., UNH(Z2C)), which was achieved with Ce atom substituting for a portion of Zr atom within the Zr-oxo clusters. Pt nanoparticles (NPs) are integrated with MOFs to form composites using the dual-solvent method. Ce-oxo fulfills a bifunctional role: it not only facilitates the enhancement of the ligand-to-metal charge transfer (LMCT), but also establishes interaction with Pt NPs. Ce-oxo mediates an enhancement of electron density on Pt NPs. This phenomenon enhances the adsorption and activation of oxygen, significantly boosting the photocatalytic performance for toluene degradation, as demonstrated by a reduction of 30 ℃ for complete mineralization of toluene as compared to that of Pt@UiO-66-NH2(Zr) (i.e., PUNH(Zr)). This study potentially offers new insights into the relationship between electron transfer effects in bimetallic MOF-based catalysts and their efficient catalytic performance for VOCs degradation.

Boosting the catalytic performance of MnOx in acetone oxidation by weakening the Mn[sbnd]O bond strength

Manganese oxides (MnOx) exhibit considerable potential in the catalytic degradation of volatile organic compounds (VOCs) due to their excellent catalytic activity, superior stability and economic cost. In this work, a two-step calcination strategy was developed to prepare MnOx/CeO2 catalysts with low MnO bond strengths and highly active lattice oxygens. The obtained Mn4Ce1-NA after the optimization has a smaller grain size, enhanced specific surface area and weakened MnO bonds, which is attributed to the in situ restriction of the manganese oxides by the two-step calcination. Moreover, the entrance of Ce into the MnOx lattice further weakened the MnO bonds, leading to superior low-temperature reducibility and lattice oxygen activity, which effectively promoted the catalytic activity of the catalysts. The optimal samples displayed outstanding acetone degradation performance, capable of completing 90 % acetone conversion at 172 °C. The catalyst also exhibits excellent stability, with the conversion of acetone maintained at around 95 % for 64 h. This work contributes to a deeper understanding of reactive oxygen species in the catalytic oxidation of VOCs, while providing a new strategy for the rational design of efficient catalysts for the oxidation of VOCs.

A Critical Review of Deep Oxidation of Gaseous Volatile Organic Compounds via Aqueous Advanced Oxidation Processes.

Volatile organic compounds (VOCs) are considered to be the most recalcitrant gaseous pollutants due to their high toxicity, diversity, complexity, and stability. Gas-solid catalytic oxidation methods have been intensively studied for VOC treatment while being greatly hampered by energy consumption, catalyst deactivation, and byproduct formation. Recently, aqueous advanced oxidation processes (AOPs) have attracted increasing interest for the deep oxidation of VOCs at room temperature, owing to the generation of abundant reactive oxygen species (ROS). However, current reviews mainly focus on VOC degradation performance and have not clarified the specific reaction process, degradation products, and paths of VOCs in different AOPs. This study systematically reviews recent advances in the application of aqueous AOPs for gaseous VOC removal. First, the VOC gas-liquid mass transfer and chemical oxidation processes are presented. Second, the latest research progress of VOC removal by various ROS is reviewed to study their degradation performances, pathways, and mechanisms. Finally, the current challenges and future strategies are discussed from the perspectives of synergistic oxidation of VOC mixtures, accurate oxidation, and resource utilization of target VOCs via aqueous AOPs. This perspective provides the latest information and research inspiration for the future industrial application of aqueous AOPs for VOC waste gas treatment.

How the Most Neglected Residual Species in MOF-Based Catalysts Involved in Catalytic Reactions to Form Toxic Byproducts.

In recent years, multifarious new materials have been developed for environmental governance. Thereinto, metal organic framework (MOF)-based catalysts have been widely employed for heterogeneous catalysis because of their high porosity to confine noble metal particles faraway from aggregation. However, the potential reactions between residual species from the material synthesis process and target pollutants, which could form highly toxic byproducts, are often neglected. Herein, we took the widely used Zr-MOF, UiO-66, with highly thermal stability supported Pd catalysts as the example to investigate how the residual species in catalysts are involved in aromatic volatile organic compounds (VOCs) degradation reaction. The results showed that residual Cl species originated from the ZrCl4 metal precursor participated in the VOC degradation reaction, leading to the production of various chlorine-containing byproducts, even the hypertoxicity dioxin precursor, dichlorobenzene. Meanwhile, the chlorination mechanism for the formation of chlorine-containing byproducts was revealed by density functional theory calculation. Furthermore, the highly efficient residual Cl removal approaches are proposed. Importantly, the migration and transformation of residual Cl during the degradation of five benzene series VOCs are comprehensively studied and elucidated. We anticipate that these findings will raise alarm about the neglected issue of residual species in MOF-based catalysts for heterogeneous catalysis, especially environmentally friendly catalysis.

A low-carbon dual-functional evaporator with photothermal and catalytic properties for enhanced VOCs removal during water evaporation

Solar interface distillation technologies are widely used for seawater desalination, wastewater treatment, and clean water production. However, during evaporation, volatile organic compounds (VOCs) in the water often evaporate coincidently with the water vapor, presenting a major pollutant challenge. Combining solar evaporation with advanced oxidation processes (AOP) is a potential solution for simultaneous water purification and VOC degradation. Herein, a dual-functional sponge photothermal evaporator (MBC-SA/MS) was designed to assess the efficacy of this approach. A simple porous sponge embedded with a composite catalyst, comprising MoO3−x, BiOCl, and CNT, was able to demonstrate simultaneous photothermal evaporation and catalytic degradation. MBC-SA/MS exhibited exceptional photothermal conversion efficiency and robust catalytic activity, achieving an evaporation rate of 2.1 kg m−2 h−1 under 1.0 sun intensity. Effective mitigating of phenol emissions was observed through persulfate activation resulting in 90 % phenol degradation. Life cycle assessment (LCA) confirmed this evaporator system had low environmental impact and was sustainable. This research presents a new compelling strategy for tackling VOC pollution and simultaneously enhancing water purification via solar interfacial evaporation.

A monolithic self-supporting ZnFe2O4/ZnO/ZnNi foam photocatalyst and application in the decomposition of gaseous benzene

Volatile organic compounds (VOCs) are major air pollutants which seriously affect ecological environment and pose threats to human health. In this investigation, a monolithic self-supporting ZnFe2O4/ZnO/ZNF(ZFO/ZnO/ZNF) photocatalyst was developed by in-situ growing ZnFe2O4 and ZnO on ZnNi foam (ZNF). Using benzene as a representative of the target gaseous contaminants, the optimal 5ZFO/ZnO/ZNF achieved a 99.8 % removal efficiency and 99.7 % mineralization efficiency within 20 min at an initial benzene concentration of 600 ppm under simulated sunlight irradiation. Moreover, this catalyst presents the lower ullage during gas–solid reaction, and thus enables durable recycling reuse of the photocatalyst, which still retains a 95.8 % benzene decomposition after 30th consecutive run. The mechanism studies reveal that the metal-mediated Z-type heterostructure of ZFO/ZnO/ZNF enhances rapid transportation of the photo-generated electrons and promotes redox potential, leading to the excellent photocatalytic oxidation activity and mineralization efficiency. This study highlights the potential of self-supporting monolithic metal-mediated catalysts and provides a key strategy for effective VOCs degradation.

Photo-Fenton-Active MIL-88A/CNT-Based PVA Hydrogel for Solar-Driven Water Evaporation and Simultaneous Volatile Organic Compound Removal.

Solar-driven interfacial water evaporation (SIWE) has emerged as a promising avenue for cost-effective freshwater production from seawater or wastewater. However, the simultaneous evaporation of volatile organic compounds (VOCs) presents a limitation for the widespread implementation of this technique. Thus, developing dual-functional evaporators capable of both desalining seawater and degrading VOCs is challenging. Herein, we fabricated an iron-based metal-organic framework MIL-88A/carbon nanotubes (CNTs) poly(vinyl alcohol) hydrogel (MCH) evaporator via the conventional freezing method for solar-driven seawater desalination and simultaneous photo-Fenton VOC degradation. Because of the superior photothermal conversion capability of CNTs, reduced thermal conductivity and water evaporation enthalpy within the hydrogel, and the photo-Fenton activity of rod-shaped MIL-88A, the MCH evaporator exhibits a higher evaporation rate of 2.26 kg m-2 h-1 under 1 sun illumination with simultaneous VOC degradation. The higher hydrophilicity and vertical channels in the MCH evaporator enable its self-salt cleaning ability, facilitating consistent seawater desalination, even in high salt concentrations up to 10 wt %. The synergistic effects of localized heating from CNTs and hydrogen peroxide activation through reactive sites of MIL-88A allow the MCH evaporator to degrade more than 93% of the added phenol during evaporation. This work presents a sustainable and efficient approach for solar-driven seawater desalination, offering simultaneous VOC degradation.

Transition metal in-situ doped BiOBr: Introducing oxygen vacancies to enhance hydroxyl radical generation for improved photocatalytic degradation of toluene

Photocatalytic oxidation for the removal of volatile organic compounds (VOCs) is one of the most effective and environmentally friendly means, and hydroxyl radicals with strong oxidation ability play an important role in the photocatalytic degradation of VOCs. In this paper, by selecting different transition metals (M=Co, Ni, Cu, Fe) for in situ doping modification of layered bismuth bromide oxide (BiOBr). It was found that among the catalysts Co-doped BiOBr had the highest photocatalytic degradation efficiency and mineralization rate (with 81.7 % and 64.0 %, respectively), and were significantly higher than those of BiOBr (with 51.4 % and 19.4 %, respectively). Experimental results and theoretical calculations confirmed that transition metal in situ doping modification can induce the generation of oxygen vacancy defects, while being more favorable to the adsorption and activation of H2O molecules, which leaded to the generation of a large number of hydroxyl radicals with stronger oxidative capacity and achieved the efficient photocatalytic degradation of toluene.

Enhanced photocatalytic degradation of toluene on surface C- and CN-modified TiO2 microspheres

Surface modified TiO2 materials are widely used in photocatalytic environmental purification processes. The employment of solution might exert a discernible influence on the catalyst. In this study, we incorporated tetrahydrofuran (THF) and pyrrolidine (PY) during the hydrolysis of titanium butoxide (TBOT) to modify the surface of TiO2, successfully synthesizing surface C-modified TiO2 (THF-TiO2) and surface CN-modified TiO2 (PY-TiO2) catalysts. The assistance of THF and PY not only reduced agglomeration, but also increased the specific surface area of both catalysts, leading to the exposure of more active sites in TiO2 during the photocatalytic degradation of toluene. When compared to the unsatisfactory degradation of toluene (80%) and CO2 mineralization efficiencies (40–45 %) observed using unmodified TiO2, the synthesized THF-50-TiO2 and PY-1-TiO2 microspheres demonstrated enhanced toluene degradation efficiency to 100 % and 99.8 %, respectively, and improved mineralization efficiencies to 76 % and 80 % after 120 min of ultraviolet irradiation. The experimental data and characterization results indicate that the surface-modified carbon species in THF-50-TiO2 facilitate the acceleration of electron-hole pair separation and suppress recombination. In contrast, partial nitrogen species introduced into the surface lattice of PY-1-TiO2 narrow its band gap and induce a visible light response. Overall, this study provides two methods to modify the surface of TiO2, which can be applied to prepare outstanding photocatalysts for possible application in the degradation of volatile organic compounds (VOCs) present in the air. Furthermore, it has been confirmed that solution have a significant impact on the catalyst.

Study of Pt-modified chromium-manganese oxide alloys to improve the performance of toluene abatement

This research is dedicated to solving the environmental problems of volatile organic compounds (VOCs), particularly aromatic chemicals in industrial emissions. The research aims to explore low-temperature, effective catalytic degradation technologies, specifically involving metal oxide and noble metal oxide catalysts, especially the Cr-Mn-Pt series catalysts. The Cr-Mn-Pt catalysts synthesized by the co-precipitation method showed efficient catalytic degradation of VOCs in low-temperature environments. The results of the experiment show that the Cr-Mn-Pt catalysts achieved 90 % toluene conversion at 198 °C, a 1000 ppm toluene concentration, and GHSV=15,000 mL/g·h, which is superior to single MnOx and Cr-Mn catalysts. The catalysts are characterized in depth using X-ray diffraction, specific surface area analysis and Fourier transform infrared spectroscopy. The result shows that the high specific surface area and large volume of pores of the Cr-Mn-Pt catalyst are advantageous for enhancing their catalytic activity and stability. The catalytic mechanism analysis shows that the degradation mechanism of toluene follows the Mars-van Krevelen mechanism with the final conversion of the intermediate product benzoate to CO2 and H2O. In summary, the Cr-Mn-Pt catalyst shows great potential in the technical treatment of VOCs due to their excellent low-temperature catalytic efficiency and stability, and it has enormous practical implications for protecting the environment in the industry.

Electrochemical biofilter enhances performance of volatile organic compounds abatement

ABSTRACT An electrochemical biofilter (EBF) was developed for enhancing the removal of volatile organic compounds (VOCs) through current. The removal efficiency (RE) of toluene exhibited a notable increase of 15% while the biomass growth rate exhibited a corresponding decline of 46% under an optimal current intensity of 50 mA. Meanwhile, the efficacy of the EBF system was markedly enhanced upon the removal of n-hexane, styrene, dichloromethane, and diisobutylene. The results indicated that there was an 11% to 49% increase in RE and a 0% to 64% reduction in biomass growth rates under the influence of the current. The current stimulation inhibited the accumulation of microorganisms, thereby alleviating biofilm clogging. The relative abundance of gram-positive phyla, including Firmicutes and Actinobacteria, increased by 15% and 23%, respectively, while the traditionally dominant genera within the Proteobacteria phylum, such as Rhodococcus and Dokdonella, exhibited a decline. In addition, the presence of hydrogen peroxide, free chlorine, and superoxides in the leachate indicated that the oxidative reaction increased in EBF system. This study provides an attractive pathway for current stimulation to enhance degradation of VOCs and alleviate biofilm clogging.

Efficient activation of the Co/SBA-15 catalyst by high-frequency AC-DBD plasma thermal effects for toluene removal

Dielectric barrier discharge (DBD) plasma excited by a high-frequency alternating-current (AC) power supply is widely employed for the degradation of volatile organic compounds (VOCs). However, the thermal effect generated during the discharge process leads to energy waste and low energy utilization efficiency. In this work, an innovative DBD thermally-conducted catalysis (DBD-TCC) system, integrating high-frequency AC-DBD plasma and its generated thermal effects to activate the Co/SBA-15 catalyst, was employed for toluene removal. Specifically, Co/SBA-15 catalysts are closely positioned to the ground electrode of the plasma zone and can be heated and activated by the thermal effect when the voltage exceeds 10 kV. At 12.4 kV, the temperature in the catalyst zone reached 261 °C in the DBD-TCC system, resulting in an increase in toluene degradation efficiency of 17%, CO2 selectivity of 21.2%, and energy efficiency of 27%, respectively, compared to the DBD system alone. In contrast, the DBD thermally-unconducted catalysis (DBD-TUC) system fails to enhance toluene degradation due to insufficient heat absorption and catalytic activation, highlighting the crucial role of AC-DBD generated heat in the activation of the catalyst. Furthermore, the degradation pathway and mechanism of toluene in the DBD-TCC system were hypothesized. This work is expected to provide an energy-efficient approach for high-frequency AC-DBD plasma removal of VOCs.

Boosting visible-light response for the complete decomposition of volatile organic compounds on the Cu-oxide deposited WO3 photocatalyst by the synergistic effects of TiO2

The degradation of volatile organic compounds (VOCs) by photocatalytic systems is the most practical strategy due to its cost performance, simplicity, and environmental sustainability. To address such issues, the photocatalytic activities of tungsten trioxide (WO3) were developed by the deposition of various cocatalysts. In particular, the Cu-oxide (CuO/Cu2O)-deposited WO3 (Cu-WO3) photocatalyst could efficiently decompose acetic acid and acetaldehyde into CO2 under visible-light irradiation, although it exhibited low activity for the decomposition of benzene, toluene and xylene (BTX). Furthermore, a composite Cu-WO3/TiO2 photocatalytic system, which was fabricated by the simple physical mixing of Cu-WO3 with TiO2, was found to exhibit unprecedented reactivity for the complete decomposition of persistent BTX pollutants into CO2 under visible light irradiation. The synergistic effects of Cu-WO3 and the interfacial surface complex (ISC) formed by toluene-adsorbed TiO2 contribute to the efficient visible light response by excitation up to around 600 nm. The reaction mechanism for the enhancement of photocatalytic activity by the Cu-WO3/TiO2 composite photocatalyst is examined in this study.

Performance and microbial community evolution of toluene degradation in the presence of acetone vapors using hybrid membrane-aerated biofilm reactors (HMABRs)

Biological treatment methodologies offer cost-effective and eco-friendly solutions for volatile organic compounds (VOCs) removal, but they face limitations in effectively treating hydrophobic VOCs. Herein, this study introduces the Hybrid Membrane Aerated Biofilm Reactor (HMABR) for VOC treatment. The HMABR integrates a bio-trickling filter-like spraying function with MABR technology to construct a non-submerge system. What’s more, introducing hydrophilic gases enhances the degradation of hydrophobic VOCs in pollutant biotreatment. While hydrophilic VOCs are readily degraded by microorganisms, the mechanisms of their co-degradation remain understudied. Toluene and acetone, common industrial VOCs, were examined in the HMABR system. HMABR exhibits outstanding toluene removal, reaching a maximum capacity of 142.04 gm−3h−1. The addition of acetone boosts this capacity by 70.1 gm−3h−1, altering EPS composition, and notably increasing the PN/PS ratio from 0.35 to 2.76. It can be inferred that acetone’s presence enhances biofilm EPS hydrophobicity, aiding toluene breakdown. Besides, when adding acetone, the biofilm EPS sample exhibited a more compact secondary protein structure. Analysis of the microbial community in the HMABR system identified a dominance of Pseudomonadota, with an increased abundance of Rhodanobacter, which correlated strongly with toluene degradation in the presence of acetone. Gene analysis revealed an increase in toluene degradation genes in Rhodanobacter when acetone was added. Furthermore, acetone activation was found to enhance metabolic pathways related to xylene degradation and the tricarboxylic acid (TCA) cycle, thereby improving toluene removal efficiency. These findings provide insights into co-metabolism in treating hydrophobic pollutants in HMABR and contribute to designing more effective treatment systems for VOCs.

A novel photocatalytic mechanism of volatile organic compounds degradation on BaTiO3 under visible light: Photo-electrons transfer from photocatalyst to pollutant

A novel photocatalytic mechanism of volatile organic compounds degradation on BaTiO3 under visible light: Photo-electrons transfer from photocatalyst to pollutant

A well-engineered two-dimensional coral-like architecture CNWO3 for the effective removal of volatile organic compounds from indoor air

One of the promising strategies to enhance the photocatalytic performance of graphitic carbon nitride (CN) is to establish 2D photocatalysts with boosted morphology and adjusted charge transfer direction. Herein, a green and sustainable strategy (water used as solvent) is employed to fabricate a coral-like CNWO3 with highly desirable visible-light photocatalytic activity. The coral-like structure provides more atoms at the edges and corners to act as active antennae to enhance the photocatalytic activity. These new antennae generate various active sites that are short enough to drive strong visible light harvesting, while being large enough to prevent intense quantum confinement effects. Under visible-light irradiation (λ > 400 nm), the as-prepared photocatalyst effectively removes gaseous acetaldehyde (90.5 %) and toluene (73.4 %), the two most common volatile organic compounds (VOCs) in indoor air, possibly due to its unique structure. The DFT calculations clearly show that the interaction of acetaldehyde and toluene over CNWO3 is energetically more favorable than that over CN. Both the hydroxyl (OH) and superoxide (O2−) that are generated by the photocatalyst play a substantial role in VOCs degradation. This work highlights the solar-active photocatalysis development using a synergy of morphology and material nature for sophisticated gas-phase reactions to effectively solve VOCs pollution issues of the indoor environment.

Analysis of Microwave Effects on the MnO2-Catalyzed Toluene Oxidation Pathway

Microwave radiation has become an effective catalytic combustion method, especially in the degradation of volatile organic compounds (VOCs) such as toluene using catalysts like MnO2. In this study, a spine waveguide microwave reactor was designed to investigate the influence of different microwave processing conditions on the degradation of toluene catalyzed by MnO2. An experimental system for microwave-assisted catalytic degradation of toluene was established to explore the relationship between microwave power, catalyst conductivity, and toluene degradation rate. The results showed that the efficiency of MnO2 catalyzing toluene degradation had a nonlinear relationship with microwave power, first increasing to a peak and then decreasing. Additionally, the experiment found that the degradation rate of toluene was positively correlated with the conductivity of MnO2. Subsequent characterization analyses using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy (SEM) further verified the changes in the microstructure and properties of MnO2 under microwave heating. The characterization results showed that with the increase in microwave power, the relative content of Mn3+ on the surface of MnO2 increased, and the relative content of adsorbed oxygen also increased accordingly. At a microwave power of 100 W, the treated MnO2 displayed the optimal ratio of manganese oxidation state and oxide, both close to 1:1, which was more conducive to the degradation of toluene. Based on these findings, this study hypothesized that the microwave-enhanced catalytic degradation of toluene by MnO2 may be attributed to changes in the surface electron transfer kinetics of MnO2, providing new insights into the field of microwave-enhanced catalysis.