首页> 外文学位 >New synthetic routes to catalytically active manganite, K-OMS-2 and K-OMS-2/silicon dioxide and a preliminary study on the use of a continuous flow microwave technique in the synthesis of nanosized manganese and cerium oxides and cobalt and iron oxyhydroxides.
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New synthetic routes to catalytically active manganite, K-OMS-2 and K-OMS-2/silicon dioxide and a preliminary study on the use of a continuous flow microwave technique in the synthesis of nanosized manganese and cerium oxides and cobalt and iron oxyhydroxides.

机译:催化活性锰矿,K-OMS-2和K-OMS-2 /二氧化硅的新合成途径,以及使用连续流微波技术合成纳米级锰和铈氧化物,钴和羟基氧化铁的初步研究。

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摘要

The work presented here comprises three main parts. The first part is a new route to nano-sized gamma-MnOOH (manganite). gamma-MnOOH has been synthesized via the reduction of KMnO4 with sucrose and MnSO 4 in acidic medium under refluxing conditions for four and six hours. Characterization of these manganite materials using XRD, FESEM, TEM, TGA and IR were done. The obtained manganite samples using the new route were compared against a conventionally prepared one where synthesis involved the oxidation of MnSO4 with H2O2 in basic medium. Two new synthetic methods were developed, one involving addition of KMnO4 into a solution of both sucrose and MnSO4 while the other involved addition of KMnO4 solution into sucrose followed by addition of MnSO4 (s). The latter method yielded smaller particles (up to 30 nm) than the former method (up to 80 nm) and the conventionally prepared manganite (up to 50 nm). The synthesized manganite materials exhibited promising characteristics when tested as electrocatalysts in O2 reduction. The larger particles gave higher peak currents in CV than smaller particles. When incorporated in Yardney's medium-sized lithium-air battery, the larger (up to 80 nm) particles gave higher specific capacity (up to 2.2 Ah/g), which corresponds to about 38% increase in specific energy of the battery when compared to a battery where no manganite was incorporated.;The second part of the research reported here involves the synthesis of K-OMS-2 and SiO2-supported K-OMS-2. K-OMS-2 (or OMS-2 from hereon) was successfully synthesized using a reflux method where, for the first time, oxone or KHSO5 was used as the oxidant. Nano-sized fibers with widths ranging from 8--40 nm were obtained. We also report for the first time the synthesis and catalytic activity of OMS-2 supported on SiO2 with surface area ranging from 228 to 513 m2/g and weight % OMS-2 ranging from 1.0 to 13.6%. An optimization study on styrene oxidation using OMS-2 and OMS-2/SiO2 as catalysts was done. Lowering the amount of catalyst and increasing the substrate used in the reaction significantly improved conversion and turnover frequency. Conversions of up to 81% and 19 h-1 TOF were achieved. These were the highest reports of conversion and TOF thus far for styrene oxidation using undoped OMS-2 and 24 hours reaction time. Selectivity towards the more valuable product, styrene oxide, significantly improved when OMS-2 was supported on SiO2. The weight % OMS-2 or dispersion of OMS-2 on the SiO2 support may be a key in optimizing OMS-2/SiO2 catalysts. The free-radical pathway is indeed involved in the oxidation of styrene and SiO2 contributes to the generation of epoxide-producing radicals as shown by kinetic and radical trapping experiments. Furthermore, the oxo-metal pathway may favor the production of benzaldehyde.;Finally, a preliminary study on the use of a continuous flow microwave (MW) technique to obtain inorganic nanomaterials is also presented in this thesis. Nanosized epsilon-MnO2, OMS-2, CeO2, CoOOH, and FeOOH were synthesized using the said microwave technique. Nanoplates and nanofibers of epsilon-MnO2 were obtained while mainly nanoplates of OMS-2 resulted in the use of the continuous flow MW technique. The obtained OMS-2 product was not pure. This OMS-2 was obtained with some epsilon-MnO 2. epsilon-MnO2 cannot be used as a precursor to OMS-2. Microspheres of epsilon-MnO2 can be obtained by using shorter reactors and more concentrated reactant solutions. Product yields of up to 24% were obtained in using the continuous flow MW reactor, which indicates that there are still some parameters that need to be further optimized to achieve a viable industrial process using the technique reported here. These parameters include reactor geometry, MW power, reactant concentrations, and the use of a carrier gas to alleviate clogging of the reactor. Lower product yields were obtained when the MW oven was replaced with a conventional one.
机译:这里介绍的工作包括三个主要部分。第一部分是通往纳米级MnOOH(锰矿)的新途径。通过在酸性条件下于回流条件下用蔗糖和MnSO 4还原KMnO4合成了γ-MnOOH。使用XRD,FESEM,TEM,TGA和IR对这些锰矿材料进行了表征。将使用新路线获得的锰矿样品与常规制备的锰矿样品进行比较,在常规方法中,合成涉及在碱性介质中用H2O2氧化MnSO4。开发了两种新的合成方法,一种涉及将KMnO4添加到蔗糖和MnSO4溶液中,而另一种涉及将KMnO4溶液添加到蔗糖中,然后添加MnSO4。后一种方法产生的颗粒(最大为30 nm)比前一种方法(最大为80 nm)和常规制备的锰矿(最大50 nm)更小。当作为还原O2的电催化剂进行测试时,合成的锰矿材料表现出令人鼓舞的特性。较大的颗粒比较小的颗粒在CV中提供更高的峰值电流。当安装在Yardney的中型锂空气电池中时,较大的颗粒(最大80 nm)具有更高的比容量(最大2.2 Ah / g),与之相比,电池的比能提高了约38%。第二部分是合成K-OMS-2和SiO2负载的K-OMS-2。使用回流方法成功地合成了K-OMS-2(或此处的OMS-2),其中首次使用过硫酸氢钾或KHSO5作为氧化剂。获得了宽度为8-40nm的纳米级纤维。我们还首次报道了SiO2负载的OMS-2的合成和催化活性,其表面积为228至513 m2 / g,OMS-2的重量%为1.0至13.6%。以OMS-2和OMS-2 / SiO2为催化剂,对苯乙烯氧化进行了优化研究。减少催化剂的量并增加反应中使用的底物可显着提高转化率和周转频率。转化率高达81%,TOF为19 h-1。这是迄今为止使用未掺杂的OMS-2和24小时反应时间进行的苯乙烯氧化转化率和TOF的最高报告。当OMS-2负载在SiO2上时,对更有价值的产品苯乙烯氧化物的选择性大大提高。 OMS-2的重量百分比或OMS-2在SiO2载体上的分散度可能是优化OMS-2 / SiO2催化剂的关键。自由基途径确实参与了苯乙烯的氧化,而SiO2则有助于生成环氧化物自由基,如动力学和自由基捕获实验所示。此外,氧-金属途径可能有利于苯甲醛的产生。最后,本文还对使用连续流微波技术获得无机纳米材料进行了初步研究。使用所述微波技术合成了纳米级的ε-MnO2,OMS-2,CeO 2,CoOOH和FeOOH。获得了ε-MnO2的纳米板和纳米纤维,而主要的OMS-2纳米板导致了连续流MW技术的使用。所得的OMS-2产物不是纯净的。该OMS-2是用一些ε-MnO2获得的。ε-MnO2不能用作OMS-2的前体。 ε-MnO2微球可以通过使用更短的反应器和更浓缩的反应物溶液来获得。使用连续流MW反应器可获得高达24%的产品收率,这表明仍有一些参数需要进一步优化,以使用此处报告的技术实现可行的工业过程。这些参数包括反应器的几何形状,MW功率,反应物浓度以及使用载气减轻反应器的堵塞。当用常规烤箱代替MW烤箱时,产品收率较低。

著录项

  • 作者

    Crisostomo, Vincent Mark B.;

  • 作者单位

    University of Connecticut.;

  • 授予单位 University of Connecticut.;
  • 学科 Chemistry Inorganic.;Energy.
  • 学位 Ph.D.
  • 年度 2008
  • 页码 143 p.
  • 总页数 143
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 无机化学;能源与动力工程;
  • 关键词

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