Water-Assisted Oxygen Insertion Reactions Over Supported Gold Catalysts
负载型金催化剂上的水辅助氧插入反应
基本信息
- 批准号:1465148
- 负责人:
- 金额:$ 16.06万
- 依托单位:
- 依托单位国家:美国
- 项目类别:Standard Grant
- 财政年份:2015
- 资助国家:美国
- 起止时间:2015-09-01 至 2019-08-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Due to recent advances in shale gas production, increased natural gas recovery, and reduced natural gas prices, the United States has an abundance of cheap natural gas. Methane, the primary component of natural gas, has found widespread use as a fuel for electricity generation; however it is not a good feedstock for the production of chemicals or transportation fuels such as gasoline or diesel. This stems from the difficulty in selectively oxidizing methane by insertion of an oxygen atom into a strong carbon-hydrogen bond while preventing the complete combustion to carbon dioxide and water. Gold is known to be inert when exposed to oxygen or air, but when it divided into small nanoparticles, it starts to catalyze the oxidation of carbon monoxide. Dr. Grabow of the University of Houston and Dr. Chandler of Trinity University have recently discovered a mechanism whereby water acts as a co-catalyst during CO oxidation over gold nanoparticles supported on titanium-oxide. They are now translating this knowledge to enable the partial oxidation of methane and other alkanes to form the corresponding alcohol. The team follows a collaborative and tightly coupled approach using computational and experimental studies to quantify the promotional effect of water on selective oxidation and to investigate the dominant reaction mechanism for oxygen insertion into carbon-hydrogen bonds. With over 7.72 trillion m3 of confirmed natural gas reserves, there is a huge incentive to develop commercially-viable methane conversion processes to benefit the U.S. economy and achieve national energy independence. The research activities are integrated with broad-reaching educational efforts at the K-12, undergraduate, graduate and professional level to broaden the participation of minority students and increase the retention of at-risk students at both participating universities. The University of Houston is a designated Hispanic-Serving Institution and has the most ethnically balanced student body of all major research institutions in the U.S. Trinity University provides research active undergraduate education to San Antonio and the South Texas region, which are largely populated by a traditionally underrepresented group in the STEM disciplines. Together, the principal investigators have a strong record for mentoring research projects for undergraduate, minority and female students.Dr. Lars Grabow of the University of Houston and Dr. Bert Chandler of Trinity University are funded by the Chemical Catalysis Program at NSF to study oxygen insertion reactions into carbon-hydrogen (C-H) bonds over supported gold catalysts. The ultimate goal is to convert methane to methanol selectively, and a rational approach to the problem requires the close integration of theoretical (Grabow) and experimental (Chandler) techniques. The prevailing challenge in all processes using methane as a feedstock is activating the strong C-H bond; hence, the initial focus is on higher alkanes with weaker C-H bonds to acquire pertinent knowledge about the oxygen (O) insertion mechanism. To realize the possibility of using small amounts of water to improve the activity and selectivity of oxidation reactions over supported gold (Au) catalysts, the team quantifies the amount of surface water on different supports, investigates the dominant reaction mechanism for oxygen insertion into C-H bonds, and improves the product yield as guided by computational predictions. The selected application, O insertion into C-H bonds of alkanes, is a challenging fundamental problem in chemistry with far reaching technological impact for upgrading of natural gas to benefit the U.S. economy and achieve national energy independence. This concept can also be extended to other difficult selective oxidation reactions, e.g. ethylene epoxidation. Research activities are integrated with broad-reaching educational efforts at the K-12, undergraduate, graduate and professional level to broaden the participation of minority students and increase the retention of at-risk students at both participating universities. Together, the principal investigators have a strong record for mentoring research projects for undergraduate, minority and female students.
由于最近页岩气生产的进步、天然气采收率的提高以及天然气价格的下降,美国拥有丰富的廉价天然气。甲烷是天然气的主要成分,已广泛用作发电燃料;然而,它并不是生产化学品或运输燃料(例如汽油或柴油)的良好原料。这是因为很难通过将氧原子插入强碳氢键来选择性氧化甲烷,同时防止完全燃烧成二氧化碳和水。 众所周知,金在暴露于氧气或空气时呈惰性,但当它分解成小的纳米粒子时,它开始催化一氧化碳的氧化。 休斯敦大学的 Grabow 博士和三一大学的 Chandler 博士最近发现了一种机制,在氧化钛负载的金纳米颗粒上,水充当 CO 氧化过程中的助催化剂。他们现在正在将这些知识转化为使甲烷和其他烷烃部分氧化形成相应的醇。该团队采用协作和紧密耦合的方法,利用计算和实验研究来量化水对选择性氧化的促进作用,并研究氧插入碳氢键的主要反应机制。已确认的天然气储量超过 7.72 万亿立方米,因此有巨大的动力开发商业上可行的甲烷转化工艺,以造福美国经济并实现国家能源独立。这些研究活动与 K-12、本科生、研究生和专业水平的广泛教育工作相结合,以扩大少数族裔学生的参与,并提高高危学生在两所参与大学的保留率。休斯顿大学是一所指定的拉美裔服务机构,在美国所有主要研究机构中拥有最均衡的学生群体。三一大学为圣安东尼奥和南德克萨斯地区提供研究型本科教育,这些地区主要由传统的西班牙裔人口居住。 STEM 学科中代表性不足的群体。主要研究人员在指导本科生、少数族裔和女学生的研究项目方面有着良好的记录。休斯敦大学的 Lars Grabow 和三一大学的 Bert Chandler 博士受到 NSF 化学催化计划的资助,研究负载型金催化剂上氧插入碳氢 (C-H) 键的反应。 最终目标是将甲烷选择性地转化为甲醇,解决该问题的合理方法需要理论(Grabow)和实验(Chandler)技术的紧密结合。在所有使用甲烷作为原料的工艺中,普遍面临的挑战是激活强 C-H 键;因此,最初的重点是具有较弱C-H键的高级烷烃,以获取有关氧(O)插入机制的相关知识。 为了实现使用少量的水来提高负载型金(Au)催化剂上氧化反应的活性和选择性的可能性,该团队量化了不同载体上的表面水量,研究了氧插入C-H键的主要反应机制,并根据计算预测提高产品产量。 所选择的应用是将 O 插入烷烃的 C-H 键,是化学中一个具有挑战性的基本问题,对天然气升级有深远的技术影响,从而有利于美国经济并实现国家能源独立。这个概念也可以扩展到其他困难的选择性氧化反应,例如乙烯环氧化。研究活动与 K-12、本科生、研究生和专业水平的广泛教育工作相结合,以扩大少数族裔学生的参与,并提高高危学生在两所参与大学的保留率。主要研究人员在指导本科生、少数族裔和女学生的研究项目方面有着良好的记录。
项目成果
期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Bert Chandler其他文献
Bert Chandler的其他文献
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{{ truncateString('Bert Chandler', 18)}}的其他基金
Collaborative Research: Controlling Metal-Oxide Interface Chemistry for New C-H Activation Catalysts
合作研究:控制新型 C-H 活化催化剂的金属-氧化物界面化学
- 批准号:
2329470 - 财政年份:2023
- 资助金额:
$ 16.06万 - 项目类别:
Standard Grant
FMSG: ECO: Towards Circular Manufacturing of Hydrocarbon Feedstocks from Plastic Waste
FMSG:ECO:利用塑料废物循环制造碳氢化合物原料
- 批准号:
2229168 - 财政年份:2023
- 资助金额:
$ 16.06万 - 项目类别:
Standard Grant
Collaborative Research: Tuning Hydrogen Mobility on Au/Spinel Catalysts to Develop the Isotopic Kinetic Resolution of H2 and D2
合作研究:调节 Au/尖晶石催化剂上的氢迁移率以开发 H2 和 D2 的同位素动力学分辨率
- 批准号:
2102525 - 财政年份:2021
- 资助金额:
$ 16.06万 - 项目类别:
Standard Grant
RUI: Preparation and Kinetic Characterization of New Bimetallic Au-M Selective Hydrogenation Catalysts
RUI:新型双金属Au-M选择性加氢催化剂的制备及动力学表征
- 批准号:
1566301 - 财政年份:2018
- 资助金额:
$ 16.06万 - 项目类别:
Standard Grant
RUI: Preparation and Characterization of New Heterogeneous Bimetallic Au-M Catalysts for Selective Oxidations and Hydrogenations
RUI:用于选择性氧化和加氢的新型多相双金属 Au-M 催化剂的制备和表征
- 批准号:
1300619 - 财政年份:2013
- 资助金额:
$ 16.06万 - 项目类别:
Standard Grant
RUI: Quantifying Electron Donation in Metal-Support Interactions utilizing CO Adsorption Studies and Hammet Relationships for Catalyzed Organic Transformations
RUI:利用 CO 吸附研究和催化有机转化的 Hammet 关系量化金属-载体相互作用中的电子供给
- 批准号:
1160217 - 财政年份:2012
- 资助金额:
$ 16.06万 - 项目类别:
Standard Grant
RUI: Preparation and Characterization of Dendrimer Templated Au-M Nanoparticles and Catalysts
RUI:树枝状聚合物模板 Au-M 纳米粒子和催化剂的制备和表征
- 批准号:
1012395 - 财政年份:2010
- 资助金额:
$ 16.06万 - 项目类别:
Continuing Grant
CAREER: Chemical and Catalytic Characterization of Dendrimer Templated Bimetallic Nanoparticles
职业:树枝状聚合物模板双金属纳米颗粒的化学和催化表征
- 批准号:
0449549 - 财政年份:2005
- 资助金额:
$ 16.06万 - 项目类别:
Continuing Grant
MRI: Acquisition of a Chemisorption-Physisorption Surface Area and Pore Size Analyzer for the Characterization of New Catalytic and Polymeric Materials at Trinity University
MRI:三一大学购买化学吸附-物理吸附表面积和孔径分析仪,用于表征新型催化和聚合材料
- 批准号:
0116731 - 财政年份:2001
- 资助金额:
$ 16.06万 - 项目类别:
Standard Grant
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