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高温下H-ZSM5中的碳正离子稳定性

Carbocation Stability in H-ZSM5 at High Temperature.

作者信息

Ferguson Glen A, Cheng Lei, Bu Lintao, Kim Seonah, Robichaud David J, Nimlos Mark R, Curtiss Larry A, Beckham Gregg T

机构信息

National Bioenergy Center, National Renewable Energy Laboratory , 15013 Denver West Parkway, Golden, Colorado 80401, United States.

Material Science Division, Argonne National Laboratory , 9700 South Cass Avenue B109, Lemont, Illinois 60439, United States.

出版信息

J Phys Chem A. 2015 Nov 19;119(46):11397-405. doi: 10.1021/acs.jpca.5b07025. Epub 2015 Nov 4.

Abstract

Zeolites are common catalysts for multiple industrial applications, including alcohol dehydration to produce olefins, and given their commercial importance, reaction mechanisms in zeolites have long been proposed and studied. Some proposed reaction mechanisms for alcohol dehydration exhibit noncyclic carbocation intermediates or transition states that resemble carbocations, and several previous studies suggest that the tert-butyl cation is the only noncyclic cation more stable than the corresponding chemisorbed species with the hydrocarbon bound to the framework oxygen (i.e., an alkoxide). To determine if carbocations can exist at high temperatures in zeolites, where these catalysts are finding new applications for biomass vapor-phase upgrading (∼500 °C), the stability of carbocations and the corresponding alkoxides were calculated with two ONIOM embedding methods (M06-2X/6-311G(d,p):M06-2X/3-21G) and (PBE-D3/6-311G(d,p):PBE-D3/3-21G) and plane-wave density functional theory (DFT) using the PBE functional corrected with entropic and Tkatchenko-Scheffler van der Waals corrections. The embedding methods tested are unreliable at finding minima for primary carbocations, and only secondary or higher carbocations can be described with embedding methods consistent with the periodic DFT results. The relative energy between the carbocations and alkoxides differs significantly between the embedding and the periodic DFT methods. The difference is between ∼0.23 and 14.30 kcal/mol depending on the molecule, the model, and the functional chosen for the embedding method. At high temperatures, the pw-DFT calculations predict that the allyl, isopropyl, and sec-butyl cations exhibit negligible populations while acetyl and tert-butyl cations exhibit significant populations (>10%). Moreover, the periodic DFT results indicate that mechanisms including secondary and tertiary carbocations intermediates or carbocations stabilized by adjacent oxygen or double bonds are possible at high temperatures relevant to some industrial uses of zeolite catalysts, although as the minority species in most cases.

摘要

沸石是多种工业应用中常用的催化剂,包括将酒精脱水以生产烯烃。鉴于其商业重要性,长期以来人们一直在提出并研究沸石中的反应机理。一些提出的酒精脱水反应机理显示出非环状碳正离子中间体或类似碳正离子的过渡态,并且先前的几项研究表明,叔丁基阳离子是唯一比与骨架氧结合的烃(即醇盐)对应的化学吸附物种更稳定的非环状阳离子。为了确定碳正离子在沸石的高温下(这些催化剂在生物质气相升级(约500°C)中有新应用)是否能够存在,使用两种ONIOM嵌入方法(M06 - 2X/6 - 311G(d,p):M06 - 2X/3 - 21G)和(PBE - D3/6 - 311G(d,p):PBE - D3/3 - 21G)以及采用熵校正和Tkatchenko - Scheffler范德华校正的PBE泛函的平面波密度泛函理论(DFT)计算了碳正离子和相应醇盐的稳定性。所测试的嵌入方法在寻找伯碳正离子的极小值时不可靠,并且只有仲碳正离子或更高级的碳正离子才能用与周期性DFT结果一致的嵌入方法来描述。碳正离子和醇盐之间的相对能量在嵌入方法和周期性DFT方法之间存在显著差异。根据分子、模型以及为嵌入方法选择的泛函,差异在约0.23至14.30千卡/摩尔之间。在高温下,pw - DFT计算预测烯丙基、异丙基和仲丁基阳离子的丰度可忽略不计,而乙酰基和叔丁基阳离子的丰度显著(>10%)。此外,周期性DFT结果表明,在与沸石催化剂的某些工业用途相关的高温下,包括仲碳正离子和叔碳正离子中间体或由相邻氧或双键稳定的碳正离子的机理是可能的,尽管在大多数情况下是少数物种。

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