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Relevant bibliographies by topics / Ethylene Oligomerization

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Journal articles

Academic literature on the topic 'Ethylene Oligomerization'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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Journal articles on the topic "Ethylene Oligomerization"

1

Sydora, Orson L. "Selective Ethylene Oligomerization." Organometallics 38, no. 5 (2019): 997–1010. http://dx.doi.org/10.1021/acs.organomet.8b00799.

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2

Zhang, Hongpeng, Xiangping Li, Yufei Zhang, et al. "Ethylene Oligomerization Over Heterogeneous Catalysts." Energy and Environment Focus 3, no. 3 (2014): 246–56. http://dx.doi.org/10.1166/eef.2014.1107.

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3

Albahily, Khalid, Sebastiano Licciulli, Sandro Gambarotta, et al. "Highly Active Ethylene Oligomerization Catalysts." Organometallics 30, no. 12 (2011): 3346–52. http://dx.doi.org/10.1021/om2002359.

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4

Galtier, P. A., A. A. Forestière, Y. H. Glaize, and J. P. Wauquier. "Mathematical modeling of ethylene oligomerization." Chemical Engineering Science 43, no. 8 (1988): 1855–60. http://dx.doi.org/10.1016/0009-2509(88)87053-2.

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5

Vereshchagin, S. N., N. N. Shishkina, and A. G. Anshits. "Ethylene oligomerization on phosphoric acid." Catalysis Today 13, no. 4 (1992): 651–54. http://dx.doi.org/10.1016/0920-5861(92)80104-u.

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6

Britovsek, George J. P., Robert Malinowski, David S. McGuinness, et al. "Ethylene Oligomerization beyond Schulz–Flory Distributions." ACS Catalysis 5, no. 11 (2015): 6922–25. http://dx.doi.org/10.1021/acscatal.5b02203.

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7

Nesterov, Gennadii A., Vladimir A. Zakharov, Gerhard Fink, and Wolfgang Fenzl. "Supported nickel catalysts for ethylene oligomerization." Journal of Molecular Catalysis 69, no. 1 (1991): 129–36. http://dx.doi.org/10.1016/0304-5102(91)80109-g.

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8

Liu, Yanyong. "Catalytic Ethylene Oligomerization over Ni/Al-HMS: A Key Step in Conversion of Bio-Ethanol to Higher Olefins." Catalysts 8, no. 11 (2018): 537. http://dx.doi.org/10.3390/catal8110537.

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Al-modified hexagonal mesoporous silica (HMS) materials were synthesized using dodecylamine as a template according to the methods reported in the literature. FT-IR spectra proved that Al3+ ions entered in the HMS framework in Al-HMS (prepared by sol-gel reaction) but Al3+ ions existed in the extra-framework in Al/HMS (prepared by post-modification). NH3-TPD indicated that either Al-HMS or Al/HMS had solid acid sites on the surface, and the acidic strength of Al/HMS was stronger than that of Al-HMS. For ethylene oligomerization at 200 °C under 1 MPa, Ni/Al-HMS showed an ethylene conversion of

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9

Li, Shuaikang, Zhou Lu, Weigang Fan, and Shengyu Dai. "Efficient incorporation of a polar comonomer for direct synthesis of hyperbranched polar functional ethylene oligomers." New Journal of Chemistry 45, no. 8 (2021): 4024–31. http://dx.doi.org/10.1039/d0nj05857b.

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10

Liu, Suyan, Ying Zhang, Quan Huo, Sasa He, and Yang Han. "Synthesis and Catalytic Performances of a Novel Zn-MOF Catalyst Bearing Nickel Chelating Diimine Carboxylate Ligands for Ethylene Oligomerization." Journal of Spectroscopy 2015 (2015): 1–7. http://dx.doi.org/10.1155/2015/310162.

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A novel Zn-MOF[Zn3(OH)2L2] was synthesized from dicarboxylate ligands with diimine groups (1,4-bis(4-CO2HC6H4)-2,3-dimethyl-1,4-diazabutadiene). The physicochemical properties of the material were characterized by a series of technologies including XRD, SEM, and ICP. In order to adapt to the ethylene oligomerization process, a catalyst[Zn3OH2L1Ni2](denoted as Cat.A) possessing active Ni2+centers was prepared by a postsynthetic treatment method using dichloride nickel as a nickel source in this work. For comparison,α-diimine ligands with/without dicarboxylic acid groups reacted with dichloride

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