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Biofuels production via catalytic hydrocracking of DDGS corn oil and hydrothermal decarboxylation of oleic acid over transition metal carbides supported on Al-SBA-15.

机译:通过DDGS玉米油的催化加氢裂化和油酸在Al-SBA-15上负载的过渡金属碳化物上的水热脱羧来生产生物燃料。

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摘要

The purpose of this research is to minimize the gap between the production of biofuels and the production of petroleum-based fuels by developing catalysts that can utilize renewable non-food based feedstocks (waste vegetable oils, algal oil, brown grease, etc.) and have great performance under low operation conditions.;First, the hydrocracking of distillers dried grains with solubles (DDGS) corn oil over bimetallic carbide catalysts was explored for green diesel production. A catalyst composed of nickel-tungsten (Ni-W) carbide supported on Al-SBA-15 was designed based on the ability of nickel to adsorb and activate hydrogen and the potential of tungsten for hydrogenation reactions. The catalysts showed significant differences in activity and selectivity, with the catalyst having a Ni-W ratio of 9:1 achieving 100% conversion of corn oil and 100% selectivity to diesel for 2 days. Results indicate that by minimizing metal alloy formation and enhancement of the metal dispersion leads to higher activity, selectivity, and durability of the catalysts. A dendrimer-encapsulated nanoparticle (DENP) method was employed to minimize alloy formation and increase the metal dispersion on the support. The catalysts prepared by the DENP method showed activity greater than that of the catalyst prepared by the impregnation method for the hydrocracking of DDGS corn oil.;Second, Nickel-based carbide catalysts combined with four different metals (Mo, Nb, W, and Zr) and supported on Al-SBA-15 were investigated for the hydrocracking of DDGS corn oil to produce biofuels under mild reaction conditions. The effects of the fractional sums of the electronegativities of the transition metals on the catalyst activities, selectivities, and stabilities were investigated. The closer the fractional sum of the transition metal electronegativities was to the electronegativity range of the noble catalysts (2.0-2.2), the better was the catalyst performance. The highest diesel selectivity was obtained from NiWC/Al-SBA-15, with a fractional sum of electronegativity of 2.06. The effects of doping a promoter (Ce) on the catalyst electronegativity and activity were studied. Adding Ce generally improved the catalyst performance, by adjusting the combined electronegativities nearer to 2.0-2.2. However, other parameters affected by Ce addition, such as textural properties, or the performance of individual metals could also impact catalyst performance. The NiNbC/Al-SBA-15 catalyst promoted with 5% Ce maintained stable activity for 168 h at 400 °C and 4.48 MPa H2 .;Third, several Ni-based transition metal carbide catalysts supported on Al-SBA-15 were studied for the hydrothermal decarboxylation of oleic acid and soybean oil to produce diesel range hydrocarbons with no added H 2. The effect of pre-reduction, sub-critical and super-critical water conditions on the catalyst activity and selectivity was investigated. Both the conversion of oleic acid and selectivity of decarboxylation products under super-critical conditions for each catalyst were about 2-times greater than at sub-critical conditions. In addition, the potential of these catalysts for utilizing aqueous phase reforming (APR) of glycerol for in situ H 2 production to meet process demands was demonstrated. The performance of the catalysts increases with the addition of glycerol, especially for the NiWC/Al-SBA-15 catalyst. With the addition of glycerol, the NiWC/Al-SBA-15 catalyst showed greater conversion of oleic acid and selectivity to heptadecane; however, most of the oleic acid was hydrogenated to produce stearic acid. The highest conversion of oleic acid and selectivity for heptadecane was 97.3% and 5.2%, respectively. Furthermore, the NiWC/Al-SBA-15 catalyst exhibited good potential for hydrolyzing triglycerides (soybean oil) to produce fatty acids and glycerol, and then generating H2 in situ from the APR of the glycerol produced. A complete conversion of soybean oil and hydrogenation of produced oleic acid were obtained over the NiWC/Al-SBA-15 at super-critical conditions. (Abstract shortened by UMI.).
机译:这项研究的目的是通过开发可以利用可再生的非食品基原料(废植物油,藻油,棕色油脂等)的催化剂来最大程度地减少生物燃料生产与石油基燃料生产之间的差距。在低运行条件下具有优异的性能。首先,探索了将酒糟用可溶物(DDGS)玉米油在双金属碳化物催化剂上加氢裂化以生产绿色柴油的方法。基于镍吸附和活化氢的能力以及钨在加氢反应中的潜力,设计了一种由负载在Al-SBA-15上的碳化钨(Ni-W)构成的催化剂。催化剂显示出活性和选择性的显着差异,其中Ni-W比为9:1的催化剂在2天的时间内实现了100%的玉米油转化率和100%的柴油选择性。结果表明,通过最小化金属合金的形成和金属分散体的增强,可以提高催化剂的活性,选择性和耐久性。采用树状聚合物封装的纳米颗粒(DENP)方法来最大程度地减少合金形成并增加金属在载体上的分散。用DENP方法制得的催化剂显示出比用浸渍法制得的DDGS玉米油加氢裂化催化剂更高的活性。第二,镍基碳化物催化剂与四种不同的金属(Mo,Nb,W和Zr)结合)和负载在Al-SBA-15上的DDS玉米油在温和的反应条件下加氢裂化以生产生物燃料的过程进行了研究。研究了过渡金属的电负性分数和对催化剂活性,选择性和稳定性的影响。过渡金属电负性的分数和越接近贵催化剂的电负性范围(2.0-2.2),催化剂性能越好。从NiWC / Al-SBA-15获得最高的柴油选择性,电负性的分数总和为2.06。研究了掺杂助催化剂(Ce)对催化剂电负性和活性的影响。通过将组合的电负性调节至接近2.0-2.2,添加Ce通常改善了催化剂性能。然而,受铈添加影响的其他参数,例如质地特性或单个金属的性能也可能影响催化剂性能。 5%Ce助催化的NiNbC / Al-SBA-15催化剂在400°C和4.48 MPa H2下可保持168 h的稳定活性。第三,研究了几种负载在Al-SBA-15上的Ni基过渡金属碳化物催化剂。通过油酸和大豆油的水热脱羧制备不添加H 2的柴油级烃。研究了预还原,亚临界和超临界水条件对催化剂活性和选择性的影响。在超临界条件下,对于每种催化剂,油酸的转化率和脱羧产物的选择性都比在亚临界条件下高约2倍。另外,证明了这些催化剂利用甘油的水相重整(APR)以原位生产H 2以满足工艺要求的潜力。催化剂的性能随甘油的添加而增加,特别是对于NiWC / Al-SBA-15催化剂而言。加入甘油后,NiWC / Al-SBA-15催化剂显示出更高的油酸转化率和对十七烷的选择性。然而,大多数油酸被氢化生成硬脂酸。油酸的最高转化率和庚烷的选择性分别为97.3%和5.2%。此外,NiWC / Al-SBA-15催化剂具有良好的潜力,可以水解甘油三酸酯(大豆油)以生产脂肪酸和甘油,然后从所生产的甘油的APR原位生成H2。在超临界条件下,通过NiWC / Al-SBA-15获得了大豆油的完全转化和生成的油酸的氢化。 (摘要由UMI缩短。)。

著录项

  • 作者

    Al Alwan, Basem.;

  • 作者单位

    Wayne State University.;

  • 授予单位 Wayne State University.;
  • 学科 Chemical engineering.
  • 学位 Ph.D.
  • 年度 2014
  • 页码 117 p.
  • 总页数 117
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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