Wasteomics ⇒ a workflow to analyze complex reaction environments, waste, and realistic feeds conversions



Problem statement

In most heterogeneous catalytic processes, the reactive environment contains a mixture of reactants, intermediates, and products, and some adsorbed-trapped on the catalytic surface and elsewhere. Thus, most reacting environments in catalysis are complex, involve several phases (multiphase), and comprise unstable species or are challenging to analyze. To make things worse, some of these species have (auto-)catalytic or deactivating nature on the kinetics of the surrounding ones.

A typical practice in catalysis is using model molecules or surrogates to deepen into the mechanistic pathways, microkinetics, spectroscopy, etc. Conversely, analytical techniques keep evolving, becoming more precise but always targeting a specific fraction or type of species. That is to say, there is only one technique that solves all.

We aim to bridge the fundamental research performed in our group and outside using model molecules with a powerful analytical multi-technique approach to analyze the entire reaction media. The -omics fields inspire us to reflect on the collective characterization and quantification of pools of molecules that translate into the structure, function, and dynamics involved. We apply our approach to hydrocarbon transformations and green-sustainable feedstock (i.e., waste plastics, sewage sludge, biomass, algae, and seaweed). We develop multi-technique analytical protocols for the complete chemical molecular-level description of complex mixtures.

Goals

  • Analytical workflow ⇒ multi-analytical technique integration
  • Wasteometrics I ⇒ quantitative- and molecular-level analysis
  • Wasteometrics II ⇒ data mining and processing
  • Wasteomics ⇒ reaction networks and kinetic modeling

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Related Publications

Screening hydrotreating catalysts for the valorization of a light cycle oil/scrap tires oil blend based on a detailed product analysis

by Palos, Kekalainen, Duodu, Gutierrez, Arandes, Janis, Castaño
Appl. Catal. B: Environ. Year: 2019

Abstract

Predicting the hydrotreating performance of industrial catalysts used for upgrading heavy oils is hampered by the unknown chemistry behind it. In this work, we have used a set of chromatographic and mass spectrometric techniques (APPI/ESI FT-ICR MS, FID-MS GC × GC and PFPD GC) for acquiring a more precise composition of the feed and products of the hydrotreatment of a blend of light cycle oil and scrap tire oil (20  vol%) using three benchmark catalysts: CoMo/Al2O3, NiMo/SiO2-Al2O3 and NiW/USY zeolite. Despite the different nature of the catalysts, the composition of the products was relatively similar, indicating the slower and controlled transformation of the heaviest molecules of the feed, particularly in tire oil. A faithful analysis of these molecules by combining the results of the analysis clarifies the multiple mechanisms affecting hydrotreating simultaneously: hydrodearomatization, hydrocrackinghydrodesulfurization, hydrodeoxygenation and hydrodenitrification. An effort has been made to use these results in a quantitative manner for catalyst screening.

Keywords

HPC W2C ANW