Nitrogen Chemistry and Coke Transformation of FCC Coked Catalyst during the Regeneration Process.

Sci Rep

School of Chemistry and Chemical Engineering, Pulp &Paper Engineering State Key Laboratory of China, South China University of Technology, Guangzhou 510640, China.

Published: June 2016

AI Article Synopsis

  • The regeneration of coked catalysts in fluid catalytic cracking (FCC) releases harmful gases like nitrogen and carbon oxides, posing environmental concerns.
  • Two distinct gas evolution regions during thermal decomposition were identified, stemming from aliphatic and aromatic carbons.
  • The study found different nitrogen species in FCC coke, revealing that nitrogen-containing compounds can be transformed, highlighting the potential for new technologies to reduce nitrogen oxides during regeneration processes.

Article Abstract

Regeneration of the coked catalyst is an important process of fluid catalytic cracking (FCC) in petroleum refining, however, this process will emit environmentally harmful gases such as nitrogen and carbon oxides. Transformation of N and C containing compounds in industrial FCC coke under thermal decomposition was investigated via TPD and TPO to examine the evolved gaseous species and TGA, NMR and XPS to analyse the residual coke fraction. Two distinct regions of gas evolution are observed during TPD for the first time, and they arise from decomposition of aliphatic carbons and aromatic carbons. Three types of N species, pyrrolic N, pyridinic N and quaternary N are identified in the FCC coke, the former one is unstable and tends to be decomposed into pyridinic and quaternary N. Mechanisms of NO, CO and CO2 evolution during TPD are proposed and lattice oxygen is suggested to be an important oxygen resource. Regeneration process indicates that coke-C tends to preferentially oxidise compared with coke-N. Hence, new technology for promoting nitrogen-containing compounds conversion will benefit the in-situ reduction of NO by CO during FCC regeneration.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897648PMC
http://dx.doi.org/10.1038/srep27309DOI Listing

Publication Analysis

Top Keywords

coked catalyst
8
regeneration process
8
fcc coke
8
pyridinic quaternary
8
fcc
5
nitrogen chemistry
4
coke
4
chemistry coke
4
coke transformation
4
transformation fcc
4

Similar Publications

Controllable hydrogenation of carbonyl groups (C=O) is crucial for converting furfural into high-value furfuryl alcohol. Instead of traditional impregnation method, a novel Cu-based catalyst (Cu/SiO) is prepared using the ammonia evaporation method (AE) for the efficient hydrogenation of furfural to furfuryl alcohol under mild conditions. At the reaction conditions of 90 °C and 1 MPa H, the 5Cu/SiO-AE sample showed optimal performance with higher turnover frequency (36.

View Article and Find Full Text PDF

The dry reforming of methane (DRM) could convert CH and CO into syngas, offering potential for greenhouse gas mitigation. However, DRM catalyst sintering and carbon deposition remain major obstacles. In this study, a highly dispersed PtNi alloy@Zr-doped 3D hollow flower-like MgAlO (AMO) spheres was prepared through a hydrophobic driving strategy.

View Article and Find Full Text PDF

Anchoring platinum clusters in CoP@CoNi layered double hydroxide to prepare high-performance and stable electrodes for efficient water splitting at high current density.

J Colloid Interface Sci

April 2025

Engineering Research Center of Advanced Functional Material Manufacturing of Ministry of Education, School of Chemical Engineering, Zhengzhou University, Zhengzhou, 450001 Henan, China; National Key Laboratory of Coking Coal Green Process Research, Zhengzhou University, Zhengzhou 450001, Henan, China. Electronic address:

Hydrogen production via electrocatalytic water splitting has garnered significant attention, due to the growing demand for clean and renewable energy. However, achieving low overpotential and long-term stability of water splitting catalysts at high current densities remains a major challenge. Herein, a CoP@CoNi layered double hydroxide (LDH) electrode was synthesized via a two-step electrodeposition process, demonstrating oxygen evolution reaction, with an overpotential (ƞ) of 373 mV and a Tafel slope of 64.

View Article and Find Full Text PDF

The mechanisms of NO reduction by CO over nitrogen-doped graphene (N-graphene)-supported single-atom Ni catalysts in the presence of O, HO, CO, and SO have been studied via density functional theory (DFT) modeling. The catalyst is represented by a single Ni atom bonded to four N atoms on N-graphene. Several alternative reaction pathways, including adsorption of NO on the Ni site, direct reduction of NO by CO, decomposition of NO to NO followed by reduction of NO to N, formation of active oxygen radical O*, and reduction of O* by CO, were hypothesized and the energy barrier corresponding to each of the reaction steps was calculated using DFT.

View Article and Find Full Text PDF

Direct conversion of CO with renewable H to produce methanol provides a promising way for CO utilization and H storage. Cu/ZnO catalysts are active, but their activities depend on the preparation methods. Here, we reported a facile mechanical grinding method for the fast synthesis of Cu@zeolitic imidazolate framework-8 (ZIF-8) derived Cu/ZnO catalysts applied in CO hydrogenation to methanol.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!