4.7 Article

Catalytic Degradation and Directional Upgrading of Zhunnan Lignite: Double Constraint of Active Hydrogen and Effective Acquisition of Derived Arenes over Nickel Ferrite

期刊

ENERGY & FUELS
卷 35, 期 24, 页码 19943-19952

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.energyfuels.1c02174

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资金

  1. Natural Science Foundation Research Program of Shaanxi province [2021JQ-830]
  2. General Special Project of Shaanxi Provincial Department of Education [21JK1011]
  3. Young Talent fund of University Association for Science and Technology in Shaanxi, China [20200612]
  4. Foundation of State Key Laboratory of High-efficiency Utilization of Coal and Green Chemical Engineering [2021-K01, 2021-K74]
  5. National Natural Science Foundation of China [22108237, 22068038, 21808237, 21763029]
  6. Science and Technology Foundation of Yulin [2019-82-2]
  7. Basic Research Program of Jiangsu Province [BK20180642]

向作者/读者索取更多资源

A novel magnetic nickel ferrite nanosphere prepared by hydrothermal treatment was used for catalyzing the hydrocracking of extraction residue from lignite, resulting in high yield of arenes. The introduction of NiFe2O4 led to an increase in soluble portion yield and relative content of arenes, as well as a decrease in arenol content. The ability of NiFe2O4 to degrade high-heteroatom species to low-heteroatom species was confirmed, indicating its effectiveness in catalytically hydrocracking lignite and upgrading derived soluble portions.
A novel magnetic nickel ferrite (NiFe2O4) nanosphere was prepared by hydrothermal treatment and used for catalyzing the hydrocracking of an extraction residue from Zhunnan lignite (ZL) to produce arenes in a high yield. The dual regulation of raising temperature and reducing hydrogen pressure effectively limits the type of generated active hydrogen species, while the synergic transfer of H center dot center dot center dot H and H center dot over NiFe2O4 facilitates the in situ cleavage of >CH-O- bridged bonds. After introducing NiFe2O4, the amplification in the soluble portion (SP) yield is 9.8%. In addition, the relative content of arenes increases from 35.3 to 49.6%, while that of arenols decreases from 35.9 to 23.3%. The analysis with a quadrupole exactive orbitrap mass spectrometer further confirmed that NiFe2O4 has the ability to degrade the high-heteroatom (HA)-number species to the low-HA-number species in situ. Therefore, the easily recoverable NiFe2O4 is effective for catalytically hydrocracking ZL and upgrading the derived SPs.

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