Modulation of the Acidity of HY, HBETA, and HZSM‐5 Zeolites by Lanthanum Incorporation for Selective Gasoline Desulfurization in the FCC Riser

Abstract This study evaluates the incorporation of lanthanum into zeolites Y, Beta, and ZSM‐5 to promote the desulfurization of a gasoline stream directly in the riser of a fluid catalytic cracking (FCC) process. The catalysts were prepared using wet impregnation and characterized by X‐ray diffraction (XRD) (crystallinity and phase integrity), XRF (La content and Si/Al ratio), X‐ray photoelectron spectroscopy (XPS), solid state nuclear magnetic resonance (NMR) of 2 ⁹Si and 2 ⁷Al, N 2 adsorption, high‐resolution transmission electron microscopy (HRTEM), temperature‐programmed desorption of ammonia (TPD‐NH 3 ), Fourier‐transform infrared spectroscopy (FTIR), and pyridine chemisorbed FTIR (FTIR‐Py). Catalytic tests were conducted in a tubular reactor, using a mixture of cyclohexane and thiophene (20000 ppm) at 773 K and 1.3 atm. Catalytic activity was assessed in a fixed‐bed reactor using a cyclohexane/thiophene feed, and product selectivities were quantified by gas chromatography with flame ionization and sulfur chemiluminescence detectors. The addition of lanthanum altered the acidity of the catalysts, reducing the total density of acid sites while increasing the strength of Lewis acid sites. The protonated zeolites, particularly HY, facilitated sulfur removal, achieving a 91% selectivity for H 2 S through secondary hydrogen transfer reactions. In contrast, the lanthanum‐modified zeolites enhanced thiophene alkylation and condensation reactions, as evidenced by the selectivity observed in La/BEA and La/ZSM‐5, which reached 15%. The results indicated that incorporating lanthanum changes the desulfurization profile, making the catalysts more selective for forming higher molecular weight sulfur compounds, thereby shifting the products toward the FCC diesel range. The modulation of acidity and structural accessibility of the zeolites proves crucial in converting sulfur compounds into H 2 S or heavy sulfur compounds in the FCC riser, leading to a reduction in the sulfur content of the gasoline fraction, which is economically advantageous.

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Publication Details

Journal
ChemCatChem
Published
2025-08-28
DOI
https://doi.org/10.1002/cctc.202500888
Citations
4
Primary Topic
Catalysis and Hydrodesulfurization Studies
Type
article
Field-Weighted Citation Impact
2.85

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article

Modulation of the Acidity of HY, HBETA, and HZSM‐5 Zeolites by Lanthanum Incorporation for Selective Gasoline Desulfurization in the FCC Riser

Agustı́n Martı́nez, Daniel Freire Almeida, Alice Caroline Alves da Silva, José Marcos Moreira Ferreira et al.
4 citations
ChemCatChem
Catalysis and Hydrodesulfurization Studies
2.85
article

Modulation of the Acidity of HY, HBETA, and HZSM‐5 Zeolites by Lanthanum Incorporation for Selective Gasoline Desulfurization in the FCC Riser

Agustı́n Martı́nez, Daniel Freire Almeida, Alice Caroline Alves da Silva, José Marcos Moreira Ferreira, Enrique Rodrı́guez-Castellón, Daniel Ballesteros‐Plata, Luiz Antônio Magalhães Pontes, Ronaldo Costa Santos, Y.L. Lam
article en
4 citations

Abstract

Abstract This study evaluates the incorporation of lanthanum into zeolites Y, Beta, and ZSM‐5 to promote the desulfurization of a gasoline stream directly in the riser of a fluid catalytic cracking (FCC) process. The catalysts were prepared using wet impregnation and characterized by X‐ray diffraction (XRD) (crystallinity and phase integrity), XRF (La content and Si/Al ratio), X‐ray photoelectron spectroscopy (XPS), solid state nuclear magnetic resonance (NMR) of 2 ⁹Si and 2 ⁷Al, N 2 adsorption, high‐resolution transmission electron microscopy (HRTEM), temperature‐programmed desorption of ammonia (TPD‐NH 3 ), Fourier‐transform infrared spectroscopy (FTIR), and pyridine chemisorbed FTIR (FTIR‐Py). Catalytic tests were conducted in a tubular reactor, using a mixture of cyclohexane and thiophene (20000 ppm) at 773 K and 1.3 atm. Catalytic activity was assessed in a fixed‐bed reactor using a cyclohexane/thiophene feed, and product selectivities were quantified by gas chromatography with flame ionization and sulfur chemiluminescence detectors. The addition of lanthanum altered the acidity of the catalysts, reducing the total density of acid sites while increasing the strength of Lewis acid sites. The protonated zeolites, particularly HY, facilitated sulfur removal, achieving a 91% selectivity for H 2 S through secondary hydrogen transfer reactions. In contrast, the lanthanum‐modified zeolites enhanced thiophene alkylation and condensation reactions, as evidenced by the selectivity observed in La/BEA and La/ZSM‐5, which reached 15%. The results indicated that incorporating lanthanum changes the desulfurization profile, making the catalysts more selective for forming higher molecular weight sulfur compounds, thereby shifting the products toward the FCC diesel range. The modulation of acidity and structural accessibility of the zeolites proves crucial in converting sulfur compounds into H 2 S or heavy sulfur compounds in the FCC riser, leading to a reduction in the sulfur content of the gasoline fraction, which is economically advantageous.

ChemCatChemVol. 17(21)
Universidade Federal do Rio de Janeiro (BR), Universidade Federal da Bahia (BR), Serviço Nacional de Aprendizagem Industrial (BR), Instituto Brasileiro de Informação em Ciência e Tecnologia (BR), Universidade Veiga de Almeida (BR), Instituto de Tecnología Química (ES), Universidade Salvador (BR), Universidad de Málaga (ES)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Ministerio de Ciencia e Innovación, Agência Nacional do Petróleo, Gás Natural e Biocombustíveis, European Regional Development Fund, Agencia Estatal de Investigación
Openalex Percentile: Top 9%
Catalysis and Hydrodesulfurization Studies
2.85
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