Klushin, Victor А.
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Oligomerization of Fischer-Tropsch Olefins by Radical Initiation Method for Synthesizing Poly Olefin Base Oils Kataria, Yash Vijay; Kashparova, Vera P.; Klushin, Victor А.; Papeta, Olga P.; Yakovenko, Roman E.; Zubkov, Ivan N.
Bulletin of Chemical Reaction Engineering & Catalysis 2024: BCREC Volume 19 Issue 3 Year 2024 (October 2024)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.20205

Abstract

In the present work we have investigated the oligomerization process of Fischer-Tropsch synthesis products – gasoline (C5-C10) and diesel (C11-C18) hydrocarbon fractions with a total olefin content (consisting mainly olefins with a branched isomeric chain) of 79.3 and 31.8 wt.%, respectively. Oligomerization was carried out by radical initiation method using azobisisobutyronitrile, benzoyl peroxide, dicumyl peroxide and methyl ethyl ketone peroxide (Butanox M-50) as initiators. It was established that the yield of the oligomerization process depending on the initiator used decreases in the following order: azobisisobutyronitrile > benzoyl peroxide > dicumyl peroxide > Butanox M-50. It was determined that when the oligomerization is carried out in polar solvents such as acetone and dichloromethane the yield of product increases by ~2.1 and ~1.7 times, respectively, while at the same time adding a non-polar solvent such as tetrachloromethane to the reaction mixture decreases the product yield by ~2.0 times. The optimal technological parameters for carrying out oligomerization process of synthetic gasoline and diesel fractions were determined: where azobisisobutyronitrile, content 0.5 wt.%., is used as an initiator, acetone as solvent, with reaction temperature of 200 °C, and duration of 12 hrs. under inert atmosphere. The product yield from the diesel fraction is 39.5 %, and from the synthetic gasoline fraction – 36.0 %. At the same time, in terms of characteristics, the oligomerization product of the diesel fraction showed properties similar to commercially available Base oil 3cSt (Group III), and the gasoline fraction showed properties on par with the commercially produced PAO-2 (Group IV). Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).
Oxidative Oligomerization of Fischer–Tropsch Internal Olefins Catalyzed by Metal Octoates of s, p and d Block Elements Kataria, Yash Vijay; Lavrenov, Sergey A.; Yakovenko, Evgeniya Yu.; Klushin, Victor А.; Yakovenko, Roman E.; Kashparova, Vera P.; Zubkov, Ivan N.
Bulletin of Chemical Reaction Engineering & Catalysis 2025: BCREC Volume 20 Issue 3 Year 2025 (October 2025)
Publisher : Masyarakat Katalis Indonesia - Indonesian Catalyst Society (MKICS)

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.9767/bcrec.20363

Abstract

In the present work we further expanded the scope of the study of the oxidative oligomerization process of synthetic hydrocarbon fraction obtained by Fischer–Tropsch synthesis with a total olefin content (consisting predominantly internal/branched olefins) of 10 % with the aim of producing poly-α-olefin like lubricant material. The oxidative oligomerization was carried out using commercially available metal octoates based on Co, Mn, Zn, Ca, Ba, Li, Zr, Cu and Pb and their combinations as catalyst. It was established that the yield of the oligomerization reaction depending on the active metal component used decreased in the following order: Ba > Zr > Zn > Co > Mn > Ca > Li > Cu > Pb. While at the same time, the oxidative oligomerization reaction carried out using bimetallic catalytic systems did not led to any significant increase in the product yield. The oxidative oligomerization reaction using Ba octoate as catalyst gave a yield of 30.4 % and had a kinematic viscosity at 100 °C of 3.6 cSt, Viscosity Index value of 201 and pour point of minus 10. Copyright © 2025 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).