Effect of the Method of Synthesizing a Nickel-Containing Catalyst on Lignin Conversion in Liquid-Phase Hydrodepolymerization
- 作者: Arapova O.V.1, Ellert O.G.2, Borisov R.S.1, Chistyakov A.V.1, Vasil’kov A.Y.3, Tsodikov M.V.1, Gekhman A.E.2
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隶属关系:
- Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences
- Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
- Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
- 期: 卷 59, 编号 1 (2019)
- 页面: 111-119
- 栏目: Article
- URL: https://journal-vniispk.ru/0965-5441/article/view/180703
- DOI: https://doi.org/10.1134/S0965544119010055
- ID: 180703
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详细
Results of the catalytic hydrogenation of lignin in a hydrogen-donor solvent medium are described. Nickel-containing systems are deposited directly on the lignin surface in an amount of 1.5–3.4 wt %. Nickel systems are deposited by two methods: from a Ni(OAc)2 × 4Н2О aqueous solution and from a colloidal solution in toluene of nickel particles prepared by metal vapor synthesis (MVS). The hydrogen donor solvent is tetralin taken in a tetralin/lignin ratio of 1 : 1. Hydrogenation was carried out in a rotating autoclave at a temperature of 400°C and a pressure of 100 atm. It is shown that the preactivation of nickel-containing lignin by ultrasonication at 39 kHz for 20 min leads to an almost exhaustive conversion of the organic matter: the hydrogenation products comprise 13.1 wt % gas and 86.3 wt % liquid hydrocarbons. The liquid hydrogenation products contain aromatic hydrocarbons and nonvolatile condensed compounds with an average molecular weight of 300 Da. The effect of sonication on nickel-containing lignin and the evolution of nickel-containing components during lignin hydrodepolymerization are studied by electron microscopy and magnetic susceptibility methods.
作者简介
O. Arapova
Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences
编辑信件的主要联系方式.
Email: arapova@ips.ac.ru
俄罗斯联邦, Moscow
O. Ellert
Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
Email: arapova@ips.ac.ru
俄罗斯联邦, Moscow
R. Borisov
Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences
Email: arapova@ips.ac.ru
俄罗斯联邦, Moscow
A. Chistyakov
Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences
Email: arapova@ips.ac.ru
俄罗斯联邦, Moscow
A. Vasil’kov
Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences
Email: arapova@ips.ac.ru
俄罗斯联邦, Moscow
M. Tsodikov
Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences
Email: arapova@ips.ac.ru
俄罗斯联邦, Moscow
A. Gekhman
Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences
Email: arapova@ips.ac.ru
俄罗斯联邦, Moscow
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