Manganese Oxide Octahedral Molecular Sieves Research Articles

Efficient ozone decomposition in high humidity environments using novel iron-doped OMS-2-loaded activated carbon material.

This study effectively addresses the rapid deactivation of manganese-based catalysts in humid environments during ozone decomposition by introducing iron-doped manganese oxide octahedral molecular sieve (Fe-OMS-2) catalysts supported on activated carbon (AC). By optimizing the doping ratio of Fe-OMS-2, the Fe-OMS-20.5/AC catalyst achieves nearly 100% ozone decomposition efficiency across a wide range of relative humidity levels (0 to 60%), even at elevated air flow rates of 800 L·g-1·h-1, outperforming standalone AC, Fe-OMS-2, or a simple mixture of OMS-2 and AC. The Fe-OMS-20.5/AC catalyst features a porous surface and a mesoporous structure, providing a substantial specific surface area that facilitates the uniform distribution of the Fe-OMS-2 active phase on the AC surface. The incorporation of Fe3+ ions enhances electron transfer between valence state transitions of Mn, thereby improving the catalyst's efficiency in ozone decomposition. Additionally, the AC component protects catalytic sites and enhances the catalyst's humidity resistance. In conclusion, this research presents a novel strategy for developing highly efficient and cost-effective ozone decomposition catalysts that enhance dehumidification, significantly contributing to industrial ozone treatment technologies and advancing environmental protection.

Significant enhanced SO2 resistance of Ce-doped OMS-2 catalyst by building the CeO2 shell for the low-temperature SCR of NO with NH3

Developing highly SO2-resistance catalysts for the NOx reduction at low temperatures is a significant challenge. In this study, we fabricate a catalyst of Ce-doped manganese oxide octahedral molecular sieve by building the CeO2 shell (Ce-OMS-2@CeO2) to solve this problem. This catalyst showed high selective catalytic reduction with NH3 (NH3-SCR) activity and enhanced resistance to SO2-induced deactivation. Ce-OMS-2@CeO2 exhibited outstanding NH3-SCR activity and anti-sulfur performance at 200 °C. The mesoporous CeO2 shells exerted no influence on the transport of reactants to catalytic active sites. The NH3-SCR on Ce-OMS-2@CeO2 catalyst occurred via the Langmuir-Hinshelwood mechanism with adsorption of NH3 and NO on different sites, thus preventing competing adsorption. The CeO2 shell bound SO2 strongly in priority, thus protecting the Ce-OMS-2 core from SO2 poisoning. Moreover, a dynamic balance was established between NH4HSO4 formation and decomposition over our Ce-OMS-2@CeO2 catalyst at low temperatures, which also hindered the SO2 poisoning in NH3-SCR reaction.

Enhancing CO catalytic oxidation performance over Cu-doping manganese oxide octahedral molecular sieves catalyst

The CO oxidation catalytic activity of catalysts is strongly influenced by the oxygen vacancy defects (OVDs) concentration and the valence state of active metal. Herein, a defect engineering approach was implemented to enhance the oxygen vacancy defects and to modify the valence of metal ions in manganese oxide octahedral molecular sieves (OMS-2) by the introduction of copper (Cu). The characterization and theoretical calculation results reveal that the incorporation of Cu2+ ion into the OMS-2 structure led to a rise in specific surface area and pore volume, weakening of Mn-O bonds, higher proportion of the low-coordinated oxygen species adsorbed in oxygen vacancies (Oads) and an increase in the average oxidation state of manganese. These structural modifications were discovered to considerably reduce the apparent activation energy (Ea), thus ultimately significantly enhancing the CO oxidation activity (T99 at 148 ℃at GHSV = 13,200 h−1) than the original OMS-2 (T99 = 215 ℃ at GHSV = 13,200 h−1). Furthermore, In-situ diffuse reflectance infrared Fourier transform (DRIFT) and In-situ near-ambient pressure X-ray photoelectron spectroscopy (in situ NAP-XPS) results indicate that the bimetallic synergy enhanced by doping strategy accelerates the conversion of oxygen to chemisorbed oxygen species and the reaction rate of CO oxidation through Mn3++Cu2+↔Mn4++Cu+ redox cycle. The findings of this study offer novel perspectives on the design of catalysts with exceptional performance in CO oxidation.

Structure sensitivity of Cu supported on manganese oxide catalysts in levulinic acid hydrogenation

Different synthesis methods were used to prepare a series of size-controlled copper nanoparticles supported on manganese oxide octahedral molecular sieves (OMS-2) catalysts.

Enhanced Oxygen Reduction Reaction Activity of Manganese Oxide via p−d Hybridization with Aluminum Group Element Dopants

AbstractDoping engineering is an effective strategy to improve the electrocatalytic activity of manganese oxides by enhancing their poor electrical conductivity and oxygen adsorption capacity. Herein, p‐block aluminum group metal ions (Al3+, Ga3+, and In3+) are introduced into cryptomelane‐type manganese oxide octahedral molecular sieves (OMS‐2), leading to p−d orbital hybridization between the p‐orbitals of the aluminum group metals and d‐orbitals of Mn, facilitating the oxygen reduction reaction. The aluminum group metal‐doped OMS‐2 exhibits excellent catalytic activity, rapid reaction kinetics, and favorable stability compared to commercial Pt/C. Among the three prepared catalysts, Ga‐doped OMS‐2 (Ga‐OMS‐2) has stronger oxygen reduction activity. Experimental and theoretical calculations show that the superiority of Ga‐OMS‐2 is attributed to p−d hybridization, which enriches the reaction sites and enhances the binding strength of the catalyst to the O2 reaction intermediates. As a proof of concept, Zinc−air batteries assembled with Ga‐OMS‐2 as a catalyst exhibit superior power density and cycle life to commercial Pt/C. This p−d hybridization strategy gives insight into the p‐block metal doping of catalysts prepared with other transition metals with excellent electrocatalytic activity and durability for energy storage and conversion.

Structured Cerium-Manganese Catalysts Supported on Nickel Foam for Toluene Oxidation by Electric Internal Heating.

Structured catalysts are widely used in catalytic oxidation of gaseous pollutants, hot catalysis is usually needed to assist the reaction in the catalytic process. Herein, a Ce-modified manganese oxide octahedral molecular sieves (Ce-OMS-2) structured catalyst supported on foam nickel was prepared through impregnation process. A systematically quantitative testing on the toluene catalytic oxidation effectiveness of this structured catalyst was conducted through catalyst evaluation device, combining a series of characterization methods, such as XRD and SEM, the structure-activity relationship was established. Assisted with electric internal heating and ozone oxidation environments, this structured catalyst exhibits excellent catalytic oxidation performance for oxidative decomposition of toluene even under high humidity conditions. The results showed that the ozone-coupled structured nickel foam catalyst increased the decomposition efficiency of toluene from 25 % (without catalyst and heating) to 55 % (with catalyst and without heating) and the electric internal heating can significantly improve the reactivity and moisture resistance of the structured nickel-foam catalyst, at 90 % RH and 40000 h-1, 50000 ppb O3 and 40 mg/m3 toluene was maintained 100 % catalytic efficiency. The high-efficiency non-precious metal-based electrothermal catalyst prepared herein is expected to have certain enlightenment for the purification of VOCs.

Intensifying levulinic acid hydrogenation using mechanochemically prepared copper on manganese oxide catalysts

A series of copper nanoparticles supported on manganese oxide octahedral molecular sieves (OMS-2) were prepared using mechanochemical (Ball-Mill) and conventional wet-impregnation (Wet-Imp) methods. All catalysts prepared were thoroughly characterized using ICP-OES elemental analysis, X-ray diffraction (XRD), N2 sorption, H2 temperature programmed reduction (TPR) and transmission electron microscopy (TEM) techniques. The catalyst preparation methods greatly affected the size of the Cu nanoparticles. TEM images showed that 5 wt% Cu/OMS-2 (Ball-Mill) catalyst had a narrow particle size distribution with an average Cu nanoparticle size of 2.1 nm, while the corresponding 5 wt% Cu/OMS-2 catalyst prepared using wet-impregnation method had an average Cu nanoparticle size of 19.2 nm. The structural features of the catalysts were corelated with the catalytic activity using the liquid phase hydrogenation of levulinic acid (LA) to γ-valerolactone (GVL), as an exemplar process. In LA hydrogenation at 190 °C and 20 bar H2 pressure, the ball milled catalysts achieved higher LA conversion, and greater GVL yield, as compared to the corresponding catalysts prepared by wet-impregnation method, reinforcing that Cu nanoparticle size and metal dispersion are important tool to intensify the catalytic activity. For instance, 5 wt% Cu/OMS-2 (Ball-Mill) catalyst achieved almost twice the turnover frequency (TOF), 24.7 h−1 as compared to the 5 wt% Cu/OMS-2 (Wet-Imp) catalyst, TOF 11.8 h−1, under identical reaction conditions. The results of this study demonstrate that ball milling is a superior method for Cu/OMS-2 catalyst preparation than wet impregnation.

Cu incorporating into OMS-2 lattice creates an efficient Hg0 removal sorbent in natural gas with ambient-temperature H2S/H2O tolerance

Removing mercury in wet natural gas containing acidic components is essential to developing the natural gas purification industry and mitigating corrosion in aluminum heat exchangers. In this work, the Cu-doped manganese oxide octahedral molecular sieve (OMS-2) nanorods were designed for oxidation of Hg0 in wet natural gas. The Hg0 removal efficiency over Cu(0.05)-OMS-2 reached 98.2 % under a high space velocity of 24 × 104 h−1 and a complex atmosphere containing H2O, CO2, and H2S. Surface reactive oxygen species produced by strong electronic interactions owing to Mn-O-Cu hybridization was the main active sites for Hg0 oxidation. The reactive oxygen species on Cu(0.05)-OMS-2 reacted with H2S to form active sulfur species, which could combine with Hg0 to form HgS. Cu(0.05)-OMS-2 exhibited excellent ambient-temperature water resistance, which was attributed to the good redox properties caused by Cu incorporation. This work provided a new strategy for designing efficient sorbents to remove Hg0 from wet natural gas.

A new approach for the determination of As, Cu, and Pb in seawater samples using manganese oxide octahedral molecular sieve as a sorbent for dispersive solid-phase microextraction

This study introduces a novel method for preconcentrating As, Cu, and Pb from seawater samples using manganese oxide octahedral molecular sieve (OMS-2), as a sorbent, and the analysis by Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES). The OMS-2 nanomaterial was synthesized and characterized using X-ray diffraction and scanning electron microscopy, revealing a crystallite size of 20.9 nm and a typical needle-like morphology of cryptomelane structure. To optimize the ICP-OES operating conditions and the preconcentration process, a central composite design was used. The optimal conditions for ICP-OES analyses were 1200 W and 0.7 L min−1 for the levels of the radio frequency potential (RF) and nebulization gas flow rate, respectively. The optimal conditions for the adsorption process were achieved at a pH of 6.5, 30 mg of OMS-2, and 35 min of stirring time, in the presence of the sample matrix. The enrichment factors obtained were 66, 45, and 21, and a limit of detection of 0.3, 0.1, and 2.1 μg L−1 for As, Cu, and Pb, respectively. The recovery tests ranged from 80 % to 120 %. The method was successfully applied to determine As, Cu, and Pb in seawater samples.

Size Effect of Platinum Nanoparticles over Platinum-Manganese Oxide on the Low-Temperature Oxidation of Toluene.

The effect of size of Pt nanoparticles has an important influence on the performance of supported Pt-based catalysts for the elimination of toluene. Herein, uniform Pt nanoparticles with average sizes of 1.5, 2.0, 2.5, 2.9, and 3.6 nm were obtained and supported on manganese oxide octahedral molecular sieves (OMS-2), and their catalytic performances for toluene oxidation were evaluated. Benefiting from the moderate interfacial interaction between nanoparticles and manganese oxide support, Pt/OMS-2-3 with the Pt particle size of 3.0 nm showed the best catalytic performance owing to the highest content of Pt2+ species. It also facilitates the formation of more abundant Mnδ+ (Mn2+ and Mn3+) and oxygen vacancies than that of the other sizes of the OMS-2-supported Pt nanoparticles, which can be filled by a large amount of adsorbed oxygen and converted into reactive oxygen species. We further showed that the resulting surface synergetic oxygen vacancies (Pt2+-Ov-Mnδ+) play a decisive part in catalyzing the complete oxidation of toluene. The result will provide new insights for designing efficient Pt-based catalysts for deep purification of toluene.

TiN nanoparticles/OMS-2 nanorods/carbonized wood composites for simultaneous solar water evaporation and abatement of volatile organic compound from undrinkable water

Severe air pollution, water pollution, and climate change have led to an increasing shortage of clean water. Solar interface water evaporation is becoming important to obtain distilled water from undrinkable water such as seawater and contaminated water. However, the as-obtained distilled water usually contains excessive volatile organic compounds (VOCs), which are serious harmful to human health. In this article, a novel bi-functional material is prepared by depositing manganese oxide octahedral molecular sieve (OMS-2) nanorods on carbonized wood (CW), which can simultaneously realize solar water evaporation and VOCs abatement. OMS-2 nanorods synthesized at lower hydrothermal temperature possess higher oxygen vacancy defects, which can improve not only the solar absorption and solar water evaporation rate but also solar driven photothermo-catalytic activity for the oxidation of VOCs. Doping TiN nanoparticles into CW/OMS-2 can further enhance the solar water evaporation performances and VOCs removal efficiencies because of its excellent solar absorption ability, which can further increase the temperature of OMS-2 catalyst and accelerate the solar water evaporation and the toluene degradation. The as-designed bifunctional composites possess an outstanding water evaporation rate over 1.436 kg m−2 h−1 and a toluene removal efficiency of 92.96% under 2.5 sun irradiation, indicating exciting prospects for efficiently producing clean water from undrinkable water with VOCs.

Magnesium doping to improve the light to heat conversion of OMS-2 for formaldehyde oxidation under visible light irradiation

Mg-doped manganese oxide octahedral molecular sieve (Mg-OMS-2) catalysts were prepared by hydrothermal method. The photothermal degradation performance of these catalysts for formaldehyde (HCHO) in batch system and continuous system was investigated. The light absorption of OMS-2 was increased by Mg-doped, especially for near infrared light, which promoted surface temperature reach a maximum of 214.8 °C under xenon irradiation. At this temperature, the reinforced surface lattice oxygen and oxygen vacancy that formed by lattice distortion via Mg-doped were activated. The best HCHO elimination efficiency was achieved over Mg0.2/OMS-2 catalyst with Mg2+/Mn2+ = 1/5, which could reduce HCHO from 250 ppm to 10 ppm within 20 min. The in situ DRIFTS was also carried out to monitor the changes in the content of reaction intermediates and analyze the degradation paths of HCHO. It was found the HCHO was attacked by formed •OH and •O2− to generate formate species and carbonate species, and finally transformed to CO2 and H2O. This photothermal catalytic oxidation process exhibited a high efficiency purification of HCHO without the help of extra energy consumption.

Synthesis of Ag-OMS Catalyst for Sunlight-Assisted Photodegradation of Crystal Violet Dye

The contamination of water with organic pollutants, such as dyes, has become a serious threat to the environment. Therefore, the development of a cost-effective, eco-friendly, proficient, and visible-light-driven catalyst for the treatment of organic dye-contaminated wastewater has been a burning issue recently. Photocatalysis is suggested as a potential treatment technique for the eradication of organic pollutants. The 1D tunnel-structured manganese oxide octahedral molecular sieve (OMS) is a suitable substance to be tested as a visible-light-driven photocatalyst for the degradation of organic contaminants. However, the fast recombination of photoinduced charges (h+/e−) limits its photocatalytic application. The development of heterojunctions between OMS and other metals, such as Ag, is a suitable technique for improving the photocatalytic performance of OMS. In this study, Ag-OMS with plasmon-enhanced photocatalytic activity is reported for the photodegradation of crystal violet dye. Manganese oxide OMS was prepared by an acidic precipitation method using potassium permanganate, manganese acetate, and nitric acid as precursor materials. Ag nanoparticles were deposited on OMS using leaf extracts of Calotropis gigantea. The deposition of Ag enhanced the photocatalytic performance of OMS from 68 to 95%. The effects of Ag contents, catalyst dosage, and concentration of crystal violet dye on catalytic performance were explored as well. Approximately 100, 95, and 75% photodegradation of 50, 100, and 150 mg/L crystal violet dye was observed in 90, 120, and 120 min in the presence of 10% Ag-OMS, respectively. Excellent photocatalytic performance, low dose utilization, and reusability proved that Ag-OMS might have practical environmental applications.

Cu Species-Modified OMS-2 Materials for Enhancing Ozone Catalytic Decomposition under Humid Conditions.

Manganese oxide octahedral molecular sieves (OMS-2) exhibit an excellent performance in ozone catalytic decomposition in dry atmosphere conditions, which however is severely limited by deactivation in humid conditions. Herein, it was found that the OMS-2 materials modified with Cu species could obviously improve both the ozone decomposition activity and water resistance. Based on the characterization results, it was found that these CuOx/OMS-2 catalysts exhibited dispersed CuOx nanosheets attached and located at the external surface accompanied with ionic Cu species entering the MnO6 octahedral framework of OMS-2. In addition, it was demonstrated that the main reason for the promotion of ozone catalytic decomposition could be ascribed to the combined effect of different Cu species in these catalysts. On the one hand, ionic Cu entered the MnO6 octahedral framework of OMS-2 near the catalyst surface and substituted ionic Mn species, resulting in an enhanced mobility of surface oxygen species and formation of more oxygen vacancies, which act as the active sites for ozone decomposition. On the other hand, the CuOx nanosheets could serve as non-oxygen vacancy sites for H2O adsorption, which could alleviate the catalyst deactivation to some extent caused by the occupancy of H2O on surface oxygen vacancies. Finally, different reaction pathways for ozone catalytic decomposition over OMS-2 and CuOx/OMS-2 under humid conditions were proposed. The findings in this work may shed new light on the design of highly efficient catalysts for ozone decomposition with improved water resistance.

Identifying the promotional mechanism for the activity and SO2 resistance of Ce-doped K-OMS-2 for the low-temperature SCR of NO with NH3

Mn-based catalysts for the low-temperature selective catalytic reduction (SCR) of NOx by NH3 can be strongly deactivated due to the generation of MnSO4 derived from upstream SO2 and H2O. In this study, a catalyst architecture based on a Ce-doped manganese oxide octahedral molecular sieve (Ce-OMS-2) was successfully synthesized to promote NH3-SCR activity and enhance SO2 tolerance at low temperatures. We investigated the role of Ce and its specific octahedral molecular sieve structure on the anti-SO2 poisoning effect of Ce-OMS-2. Maintaining the manganese oxide octahedral molecular sieve structure with polyvalent manganese species and active oxygen species and the charge transfer between Mn and Ce via the Ce-O-Mn bond in the Ce-OMS-2 catalyst are found to be the key factors for the realization of excellent NH3-SCR activity and SO2 tolerance. In-depth in situ diffuse reflectance infrared Fourier transform spectra (DRIFTS) show that the number of Brønsted acid sites in Ce-OMS-2 can also favor SO2 resistance. This study provides new insight into the mechanism for de-NOx activity and SO2 tolerance on Ce-OMS-2 catalyst and is beneficial for the design of anti-SO2 NH3-SCR catalysts.

Efficient toluene low‐temperature elimination over manganese oxides: Unveiling the decisive role of lattice oxygen

Manganese oxide catalysts are considered to be active in the catalytic purification of volatile organic compounds based on two theories. According to one view, defects are mainly constructed to increase the amount of adsorbed oxygen and, consequently, the catalytic activity, whereas the opposite view suggests that the mobility of lattice oxygen is the main reason for determining the catalytic performance. In order to investigate which form of oxygen is the key factor controlling the catalytic performance of manganese oxides, a series of manganese oxide octahedral molecular sieves (OMS‐2) with different adsorption and lattice oxygen properties were synthesized in this study, and the catalytic oxidation performance of the catalysts for toluene was examined. The impact of various oxygen species on the catalytic activity of OMS‐2 was investigated in depth by characterization by Raman, X‐ray diffraction, scanning electron microscope, Brunauer–Emmett–Teller, O2 temperature‐programmed desorption, H2 temperature‐programmed reduction, X‐ray photoelectron spectroscopy, and so forth. It was discovered that OMS‐2‐150 exhibits excellent catalytic activity for toluene purification due to its higher Mn4+ and lattice oxygen as well as low‐temperature reducibility. In addition, in situ diffuse reflectance, infrared Fourier transform spectroscopy also verified that lattice oxygen dominates the reaction and improves the catalytic performance. As such, in contrast to previous investigations, this study found that lattice oxygen migration was more important than adsorbed oxygen content for manganese oxides in the field of volatile organic compounds purification. This brings a new perspective to the preparation of manganese‐based catalysts with promising catalytic behaviors.

Insight into the sulfur resistance of OMS-2 modified with iron for mercury oxidation

To improve the sulfur resistance of manganese oxide octahedral molecular sieve (OMS-2) for Hg0 oxidation, OMS-2 modified by iron (Fex-OMS-2) is prepared through hydrothermal synthesis method in this study, and their Hg0 removal performance and sulfur resistance were tested in simulate flue gas. Hg0 removal efficiency of Fe0.05-OMS-2 can reach 98 % at 150 °C. Its mercury removal efficiency remains 89.2 % even in the presence of 1500 ppm SO2, while the value of OMS-2 under the same condition is only 54 %. Characterization results show that Fe0.05-OMS-2 has spinel structure with Fe2O3 wrapped on the catalyst surface which is (Mn0.983Fe0.017)2O3. Its active components both contain iron oxide and manganese oxide, which forms a double active center. Iron oxide on the catalyst surface can compete with manganese oxide for SO2 adsorption and further forms FeSO4, thus, inhibiting the sulfation of active manganese oxide and improving its sulfur resistance. Additionally, Fe0.05-OMS-2 exhibit strong water resistance, and Hg0 removal efficiency is nearly no change after the addition of 8 % H2O in the simulated flue gas.

Ag-embedded manganese oxide octahedral molecular sieve (Ag-OMS-2) nano-rods as efficient heterogeneous catalysts for hydration of nitriles to amides in aqueous solution.

Silver-embedded manganese oxide octahedral molecular sieve (Ag-OMS-2) nano-rods were synthesized using a pre-incorporation approach, and unambiguously characterized by transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA). A highly uniform distribution of Ag nanoparticles embedded in the porous structure of OMS-2, was found to be in favor of high catalytic activity of the composite for hydration of nitriles to corresponding amides in aqueous solution. By using a catalyst dosage of 30 mg per mmol of substrate, in the temperature range of 80-100 °C, and reaction times of 4-9 h, excellent yields (73-96%) of the desired amides (13 examples) were obtained. Also, the catalyst was easy to recycle, and showed a slight decrease in efficiency after six consecutive runs.

Enhanced degradation and mineralization of estriol over ZrO2/OMS-2 nanocomposite: Kinetics, pathway and mechanism

Although remarkable progresses have been achieved in the exploration of new and efficient catalytic systems for efficient degradation of estriol, there are only very few available reports providing high mineralization of estriol. Hence, it is still a serious challenge to develop the novel and efficient methods for enhanced degradation and mineralization of estriol due to its serious threat to environment and human health. Herein, this study proposes a series of ZrO2 modified manganese oxide octahedral molecular sieve (ZrO2/OMS-2) nanocomposites as efficient catalysts for enhanced degradation and mineralization of estriol via PMS activation at 30 °C. Among them, ZrO2/OMS-2-27% provided the highest degradation efficiency (95%) and mineralization degrees (70.1%), which exceeded most reported catalytic systems, in the catalytic degradation of estriol. These quenching tests and EPR analysis had confirmed that O2•- and 1O2 were primary reactive oxygen species (ROS) in the ZrO2/OMS-2-27%/PMS system, contrary to the OMS-2/PMS system for which SO4•- and OH• are primary ROS. This might be due to the abundant O-containing surface functional groups of ZrO2/OMS-2-27%. This work not only provides a facile and high-efficiency methodology for the construction of Mn-based nanomaterial, but also proposes a new and efficient nano-catalyst for estriol removal.

Revelation of Mn4+-Osur-Mn3+ active site and combined Langmuir-Hinshelwood mechanism in propane total oxidation at low temperature over MnO2

Mn-based oxides exhibit attractive catalytic activity for VOCs oxidation, but the catalytic mechanism and kinetics are still significant challenges and rarely mentioned. Therefore, we prepared OMS-2 manganese oxide octahedral molecular sieve with α-MnO2 crystal phase as model compound. By analyzing the properties of the surface chemical states of the catalysts in different reaction stages, combined with the control experiments, the coordination of Mn4+-Osur-Mn3+ was confirmed as the active site at low temperature. Meanwhile, the reaction path of propane catalytic oxidation on MnO2 surface based on condensation mechanism was proved by in-situ spectroscopy and density functional theory calculation. And kinetic studies revealed that the catalytic combustion of propane processed through Langmuir-Hinshelwood mechanism at low temperature. All these systematic study results supplied a well-defined understanding for the propane combustion over manganese oxide.