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Sythesis Of α-MnO2Nanophase And Their Application In Catalytic Oxidation Of O-xylene

Posted on:2013-10-04Degree:MasterType:Thesis
Country:ChinaCandidate:S LiFull Text:PDF
GTID:2231330395454232Subject:Organic Chemistry
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Benzene hydrocarbons (such as benzene, toluene and xylene) are the major organicvolatile compounds (VOCs) in the air. They were mainly vented form a variety of industrial,such as chemical production, mobile emission and family decorate, which cause serious harmto human health. Therefore, the removal of benzene pollutants has become an importantresearch in topic recent environmental treatments. Deep catalytic oxidation that can directlyoxidize benzene pollution into CO2and H2O is one of the most effective and promisingresearch methods. The manganese oxides are regarded as important catalysts due to theirlow-priced. Therefore preparation of the catalysts with high activity used in the completecatalytic oxidation of benzene pollutants is a very significant subject.In this paper, α-MnO2nanowires were prepared using hydrothermal method. Theα-MnO2nanowires were used for o-xylene deep catalytic oxidation. The catalytic activitieswere evaluated in term of o-xylene conversion and the yield of CO2. X-ray diffraction (XRD),Scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET), Transmission electronmicroscopy (TEM) and Energy dispersive spectrometer (EDS) were used to characterize thecatalysts. The main results are as follows:1Mesoporous α-MnO2nanowires were successfully synthesized by hydrothermalmethod based on the redox reactions of KMnO4and MnCO3. The influence of the reactiontemperature, reaction time and concentration on the product phase and morphology of theobtained α-MnO2nanowires were discussed. Experimental results showed that α-MnO2nanowires could be prepared under the conditions:10mmol KMnO4,-and10mmol MnCO3with molar ratio of n(KMnO4):n(MnCO3)=1:1, at180oC for12h. The BET results showedthat the specific area and average diameter were140.012m2·g-1and20nm, respectively,which belong to mesoporous structure. The catalyst calcined at500oC could converseo-xylene into carbon dioxide and water at200oC.2One dimensional structure of α-MnO2nanowires were successfully synthesized byhydrothermal method using potassium permanganate KMnO4and MnCO3as raw materials.The reactants conditions were as follows: n(KMnO4):n((NH4)2CO3)=1:3,120°C,12h. The influence of the reactant molar ratio, reaction temperature, reaction time and concentration onthe product phase and morphology of obtained α-MnO2nanowires with one dimensionalstructure were discussed. The CO2gas which produced by heating (NH4)2CO3play animportant role in the formation of catalyst.3On the basis of α-MnO2nanowires with one dimensional structure, the property ofcatalytic were changed by the impregnation method, such as KNO3, Ce(NO3)3·6H2O,Cu(NO3)2·3H2O, Fe(NO3)3·9H2O, Al(NO3)3·9H2O and Ni(NO3)2·6H2O solution. The resultshowed that catalysts could converse o-xylene into carbon dioxide and water at220°C、240°C、240°C、320°C、320°C and310°C.This paper was funded by the funds of national natural science (NO.21147004).
Keywords/Search Tags:Mesoporous α-MnO2, α-MnO2nanowires, Deep catalytic oxidation, o-xylene
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