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1H 和 13C 溶液-和固态 NMR 研究费托工艺中的蜡产品。

1H and 13C solution- and solid-state NMR investigation into wax products from the Fischer-Tropsch process.

机构信息

Department of Physics, University of Warwick, Gibbet Hill Road, Coventry, CV4 7AL, UK.

出版信息

Solid State Nucl Magn Reson. 2011 May-Jun;39(3-4):58-64. doi: 10.1016/j.ssnmr.2011.03.008. Epub 2011 Apr 14.

DOI:10.1016/j.ssnmr.2011.03.008
PMID:21536414
Abstract

(1)H and (13)C solid- and solution-state NMR have been used to characterise waxes produced in the Fischer-Tropsch reaction, using Co-based catalysts either unpromoted or promoted with approximately 1 wt% of either cerium or rhenium. The aim was to measure average structural information at the submolecular level of the hydrocarbon waxes produced, along with identification of the minor products, such as oxygenates and olefins, which are typically observed in these waxes. A parameter of key interest is the average number of carbon atoms within the hydrocarbon chain (N(C)). A wax prepared using an unpromoted Co/Al(2)O(3) catalyst had N(C)∼20, whilst waxes made using rhenium- or cerium-promoted Co/Al(2)O(3) catalysts were found to have N(C)∼21. All three samples contained small amounts of oxygenates and alkenes. The subtle differences found in the waxes, in particular the minor species produced, demonstrate that the different promoters have different effects during the reaction, with the Re-promoted catalyst producing the fewest by-products. It is shown in (13)C solid-state NMR spectra that for that for longer chain (compared to the lengths of chain in previous studies) waxes that the lack of resolution and the complexities added by the differential cross-polarisation (CP) dynamics mean that it is difficult to accurately determine N(C) from this approach. However the N(C) determined by (13)C CP magic angle spinning NMR is broadly consistent with the more accurate solution approaches used and suggest that the wax characteristics do not change in solution. On this basis an alternative approach for determining N(C) is suggested based on (1)H solution state NMR that provides a higher degree of accuracy of the chain length as well as information on the minor constituents.

摘要

(1)H 和(13)C 固态和溶液状态 NMR 已被用于表征使用钴基催化剂在费托反应中生产的蜡,这些催化剂未经促进或用约 1wt%的铈或铼促进。目的是测量烃蜡的亚分子水平的平均结构信息,以及鉴定通常在这些蜡中观察到的少量产物,如含氧化合物和烯烃。一个关键的感兴趣的参数是烃链内的平均碳原子数(N(C))。使用未促进的 Co/Al(2)O(3)催化剂制备的蜡的 N(C)约为 20,而使用铼或铈促进的 Co/Al(2)O(3)催化剂制备的蜡的 N(C)约为 21。所有三种样品都含有少量的含氧化合物和烯烃。在蜡中发现的细微差异,特别是产生的少量物种,表明不同的促进剂在反应中有不同的影响,其中 Re 促进的催化剂产生的副产物最少。(13)C 固态 NMR 谱表明,对于较长链(与之前研究中的链长相比)蜡,由于分辨率不足以及差分交叉极化(CP)动力学增加的复杂性,很难从这种方法准确确定 N(C)。然而,通过(13)C CP 魔角旋转 NMR 确定的 N(C)与使用的更准确的溶液方法大致一致,并表明蜡特性在溶液中不会改变。在此基础上,提出了一种基于(1)H 溶液状态 NMR 的替代方法来确定 N(C),该方法提供了更高的链长精度以及对少量成分的信息。

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