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Study on Preparation and catalytic oxidation of HDC and CO properties of the controlled structure model of metal based catalysts

Author: XuZuo
Tutor: LiHeXing; LiHui
School: Shanghai Normal University
Course: Environmental Science
Keywords: Environmental cleaning catalysis hydrodechlorination (HDC) COoxidation Ni/TiO2 Pd@SiO2 Pd-Ag/CeO2
CLC: X701
Type: PhD thesis
Year: 2012
Downloads: 169
Quote: 1
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Abstract


With the rapid society development and population growth, both the sourcedeficiency and environmental pollution have intimidated ecological equilibrium,human health and the sustainable development of society and economy. Chemicalindustry have played extremely important roles in creating the material civilization.However, at the same time, it also brings serious pollution, including air, water andsoil pollutions, among them, the air pollution has caused much more attention inenvironment cleaning since it is flexible and difficult for removing. Meanwhile, theair pollution is also an important source for inducing water and soil pollution. Themajor air pollutants include trace organic substances (POPs), inorganic oxides andheavy meatls. Aryl chlorides and carbon monoxide represent typical pollutants in air.On one hand, there are many technologies for removing aryl chlorides from air,among them, the catalytic hydrodechlorination (HDC) has received increasing interestowing to the advantages including rapid, safty and efficient pathway as well as theresource recovery from pollutants. On the other hand, catalytic oxidation of CO iscurrently a principal method for removing CO pollutant from air owing to the benefitsof easy operation, low cost and the absence of secondary pollution. Obviously, allthese reactions will proceed in the presence of metal catalysts. Accordingly, the metalcatalysts played key roles in those reactions and the enhancement of the efficiencyand lifetime of metal catalysts have become a hot topic in the current catalysis.With the development of nano science and technology, the nano effect in metalcatalysts including high surface area, quantum size effect, and volume effect etc. hasbecome more and more important. However, the tiny nanoparticles usually diplayhigh surface energy, which may induce particle agglomeration, leading to the catalystdeactivation. Meanwhile, the active phase is easily leached off during catalyticreactions, corresponding to the poor recyclability of catalysts. One of promising waysto emprove the photocatalytic performance and lifetime is the design of supportedmetal catalysts with the strong interaction between metal particles and supports.However, the supported metal catalysts obtained by traditional methods usually display large particle size and poor distribution of active phases and the weakinteraction between metals and supports. In this thesis, starting from the synthesis ofnanocatalysts, a series of efficiency and stable supported catalysts for HDC ofchlorobenzene and CO oxidation were designed by adjusting the active phases andsupports, optimizing the technology for anchoring active phases onto supports, andengineering the morphology, structure and surface chemistry, together with theexamination of the catalytic performances. Based on the detailed characterizationsand kinetic studies, the catalytic reaction mechanism and the nature of active centerstogether with the structural and electronic effects were tried to elucidate. The mainresearching work could be summarized into the following5parts.1. A novel Ni/TiO2catalyst with Ni nanoparticles embedded into TiO2mesoporous walls was synthesized through co-assembly between metallic ions andsurfactants, followed by reduction activation. In comparison with the Ni/TiO2catalystobtained by tradition impregnation-reduction method, the as-prepared Ni/TiO2catalyst exhibited enhanced efficiency and stability in gas-phase HDC ofchlorobenzene, which could be mainly attributed to the high dispersion degree of Niactive sites and the strong metal-support interaction. Moreover, the Ni nanoparticlesembedded in the TiO2mesoporous walls also exhibited strong resistance abilityagainst HCl corrosion and Ni particle agglomeration.2. A series supported Pd catalysts including Pd/SiO2, Pd/Al2O3, Pd/CeO2andPd/TiO2were designed by impregnation method and employed in catalytic oxidationof CO. The effects of reducibility and oxygen storing capacity (OSC) of varioussupports (SiO2, γ-Al2O3, CeO2and TiO2) on the catalytic performance wereinvestigataed. Experimental results demonstrated that both the high reducibility andthe enhanced OSC promoted the catalytic activity.3. Silica encapsulated Pd nanoparticles stabilized with oleylamine weresynthesized by water-in-oil microemulsion technique, followed by removal of theoleylamine molecules by calcination, leading to the core-shell structured Pd@SiO2catalyst. During CO oxidation, this catalyst exhibited much higher activity andstronger durability than the Pd catalyst deposited onto commercially available SiO2, possibly owing to the high dispersion of Pd nanoparticles and protecting effect of theSiO2outer shell on the Pd nanoparticles against agglomeration duringhigh-temperature calcinations and CO oxidation reaction.4. A novel Pd@SiO2-CeO2catalyst in core-shell morphology was prepared bydoping core-shell structured Pd@SiO2with CeO2by incipient wetness impregnationmethod. In comparison with the Pd@SiO2, the as-prepared catalyst displayed muchlower igniting temperature and higher activity in CO oxidation. The main reason wasthat the CeO2-modification could enhance the OSC and also increase the oxygenvacancies on the Pd–Ce interface, which might promote the oxygen adsorption on thecatalyst and thus, supply more active oxygen species for CO catalytic oxidation,corresponding to great enhancement in catalytic activity.5. A new Pd-Ag/CeO2bimetallic catalyst was prepared by consectiveimpregnation-calcination methods. The effects of calcination temperature, metalloadings, and Pd/Ag ratio on the catalytic performance were explored in CO oxidation,based on which the catalyst was further optimized. In comparison with either thePd/CeO2or the Ag/CeO2catalyst, the as-prepared Pd-Ag/CeO2bimetallic catalystdisplayed enhanced activity, obviously owing to the Ag-Pd synergetic effect. DuringCO oxidation, Ag and Pd could adsorb and activate O2and CO, respectively. Theirmutual promotion resulted in the enhanced activity.

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CLC: > Environmental science, safety science > Processing and comprehensive utilization of waste > General issues > Exhaust gas processing and utilization
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