• Title/Summary/Keyword: Fischer-Tropsch reaction

Search Result 42, Processing Time 0.018 seconds

Advancing the Frontier in Alkaline Promoter Performance Evaluation: Exploring Simplified Adoption Methods (알칼리 촉진제 성능 측정의 새로운 전환점: 도입 방식의 단순화를 통한 탐구)

  • Wonjoong Yoon;Jiyeon Lee;Jaehoon Kim
    • Clean Technology
    • /
    • v.30 no.1
    • /
    • pp.62-67
    • /
    • 2024
  • In this study, an alkali metal Na was introduced into iron-based catalysts used in the carbon dioxide-based Fischer-Tropsch process by wet impregnation and physical mixing methods to compare their performance. The as-prepared catalysts were evaluated for reactivity at 3.5 MPa, 330 ℃, feed ratio of H2/CO2 = 3 with a space velocity of 4,000 mL h-1 gcat-1. Comparing the two catalysts, it was found that Na was uniformly distributed throughout the catalyst when wet-impregnated, but Na for physically mixed catalyst was relatively located on the surface of the catalyst. In addition, the wet-impregnated catalyst showed higher liquid hydrocarbon (C5+) yield and lower CO selectivity. In conclusion, the effect of Na distribution in the catalyst on the reaction was identified and can be controlled by the introduction method.

The Effect of Structure and Acidity of Fluorinated HZSM-5 on Ethylene Aromatization (불소화 HZSM-5의 구조 및 산도가 에틸렌 방향족화에 미치는 영향)

  • Kyeong Nan, Kim;Seok Chang, Kang;Geunjae, Kwak
    • Applied Chemistry for Engineering
    • /
    • v.34 no.1
    • /
    • pp.15-22
    • /
    • 2023
  • Recent studies have actively investigated ways to improve the economic feasibility and efficiency of the Fischer-Tropsch process by increasing the yields of the monocyclic aromatic compounds (BTEX). In this study, ethylene was selected as a model of F-T-derived hydrocarbons, and the ethylene-to-aromatics (ETA) reaction was investigated according to changes in acid characteristics, mesopores, and crystallinity of HZSM-5 (HZ5). Fluorinated HZ5 was prepared by calcination followed by impregnation of an aqueous NH4F solution having different molar concentrations in HZ5, and the structural and chemical properties of F/HZ5 were investigated through Brunauer-Emmett-Teller (BET), solid-state nuclear magnetic resonance (NMR), X-ray photoelectron spectroscopy (XPS), NH3-temperature-programmed desorption (TPD), and pyridine-IR spectroscopy. The ETA reactions were performed at 673 K under 0.1 MPa, and fluorinating HZ5 by an aqueous NH4F solution of 0.17 M improved ethylene conversion, BTEX selectivity, and catalytic stability due to acidity, mesopore fraction, and crystallinity.