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 Covers

Related Publications

Imaging the Profiles of Deactivating-Species on the Catalyst Used for the Cracking of Waste Polyethylene by Combined Microscopies

by Castaño, Elordi, Olazar, Bilbao
ChemCatChem Year: 2012

Abstract

The catalytic cracking of high‐density polyethylene (HDPE) is an attractive process to valorize wastes throughout the production of the original monomers or fuels.1 The cracking catalyst based on zeolites is able to drive the scission of the polymeric chain, while controlling the final selectivity of monomers or fuels.2 The disadvantage of using a cracking catalyst is the deactivation caused by coke fouling, which hinders the cracking of heavy hydrocarbons and reduces the lifetime of the catalyst.3

Keywords

FCC W2C ANW