Microwave-assisted 1-decene oligomerization: In-depth analysis, kinetic insights, and thermodynamic perspectives with HY zeolite catalyst

Oligomerization of 1-olefins is a promising method for creating high-quality synthetic fuels and base oils. The optimization of 1-decene oligomerization was conducted in a micro-wave-assisted batch reactor using HY-zeolite as a catalyst. The Box-Behnken design, a response surface methodology, was em...

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Bibliographic Details
Main Authors: Muhammad Nadeem Arshad, Muhammad Faisal Irfan, Malik Abdul Rub, Mohammad Asad, Khalid A. Alzahrani, Aman Ullah
Format: Article
Language:English
Published: Elsevier 2025-07-01
Series:Results in Chemistry
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Online Access:http://www.sciencedirect.com/science/article/pii/S2211715625003935
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Summary:Oligomerization of 1-olefins is a promising method for creating high-quality synthetic fuels and base oils. The optimization of 1-decene oligomerization was conducted in a micro-wave-assisted batch reactor using HY-zeolite as a catalyst. The Box-Behnken design, a response surface methodology, was employed to optimize the reaction by varying catalyst dose (0.02–0.15 g), reaction time (5–60 min), and temperature (100–250 °C). A quadratic regression model with an R2 value above 91 % indicated a strong correlation between experimental and predicted data. The study revealed that higher temperatures and catalyst doses enhanced conversion, while extended reaction time initially boosted conversion but later caused a decline. Temperature and catalyst dose were identified as the most significant factors, while time had a statistically insignificant effect. The maximum conversion was obtained at optimal conditions of 175 °C, 30 min, and 0.11 g of catalyst. Product analysis using Gas Chromatography Mass Spectrometry, Fourier Transform Infrared Spectroscopy (FTIR), and Gel Permeation Chromatography (GPC) confirmed the formation of oligomers, with FTIR showing the disappearance of monomeric double bonds and GPC confirming oligomers with a molecular weight of approximately 700 g/mol. The kinetic study revealed an activation energy of 13.4 kJ/mol, and a reaction order of 1. The oligomerization process was determined to be endothermic, with positive adsorption enthalpy values for both dimerization and trimerization reactions.
ISSN:2211-7156