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NMR4CO2 SIGNED

Unveiling CO2 chemisorption mechanisms in solid adsorbents via surface-enhanced ex(in)-situ NMR

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EC-Contrib. €

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Partnership

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 NMR4CO2 project word cloud

Explore the words cloud of the NMR4CO2 project. It provides you a very rough idea of what is the project "NMR4CO2" about.

interfaces    lower    kinetics    solid    porous    gap    liquid    surfaces    engineers    effect    labeled    nuclear    dynamic    deactivation    industrial    sorbent    capacity    time    2017    competing    replacing    3reaching    source    elusive    regenerability    hindering    tolerant    acidic    enhanced    point    mixtures    thermodynamically    multiple    flow    formed    selectively    dioxide    tackle    removal    chemists    polarization    isotopically    chemistry    nmr4co2    inter    historic    textural    chemisorption    combustion    reaching    identification    co2    pressure    ssnmr    cycles    32    carbon    engaging    mainly    gas    fuels    regeneration    synthetic    emissions    comprising    amps    silicas    nmr    adsorption    improvement    emission    concentration    simulated    modification    continue    vi    gigatonnes    desorption    scrubbing    species    adsorbed    stability    monitoring    encompasses    fossil    expertise    combines    molecular    outcomes    situ    technologies    spectroscopists    acid    solution    nature    gases    moisture    adsorbents    selectivity    global    fill    first    ex    chemisorb    spacing    surface    amine    environmental    kinetically    decades    determines    speciation    sorbents    modified    cooperative   

Project "NMR4CO2" data sheet

The following table provides information about the project.

Coordinator
UNIVERSIDADE DE AVEIRO 

Organization address
address: CAMPUS UNIVERSITÁRIO DE SANTIAGO
city: AVEIRO
postcode: 3810-193
website: www.ua.pt

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Portugal [PT]
 Total cost 1˙999˙793 €
 EC max contribution 1˙999˙793 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-COG
 Funding Scheme ERC-COG
 Starting year 2020
 Duration (year-month-day) from 2020-06-01   to  2025-05-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSIDADE DE AVEIRO PT (AVEIRO) coordinator 1˙999˙793.00

Map

 Project objective

Reaching a historic high of 3Reaching a historic high of 32.5 gigatonnes in 2017, global carbon dioxide emissions from fossil fuels combustion continue to increase. CO2 removal technologies are part of the solution to tackle this crucial environmental challenge. Because of their lower regeneration cost, amine-modified porous silicas (AMPS) are the most promising CO2-adsorbents for replacing the decades-old liquid amine scrubbing technology. AMPS are “moisture-tolerant” and selectively chemisorb CO2 from low-concentration mixtures, important features for operating under large-point CO2 emission source conditions. The nature of CO2 species formed on AMPS surfaces determines the gas adsorption capacity/kinetics, selectivity, stability, and regenerability. However, a molecular-scale understanding of the CO2-AMPS adsorption process remains elusive, hindering our ability to design improved sorbents. NMR4CO2 aims to fill in this gap, engaging for the first time state-of-the-art surface-enhanced ex- and in-situ solid-state NMR (SSNMR) to study the chemistry of acidic gases (mainly CO2) adsorbed on AMPS, and the gas-solid interfaces, using simulated industrial gas mixtures. The project combines the expertise of spectroscopists, chemists, and engineers to tackle these challenges. NMR4CO2 encompasses the design of novel SSNMR methods to study the kinetically- and thermodynamically-driven CO2-AMPS adsorption process, comprising in-situ flow NMR, dynamic nuclear polarization NMR, and isotopically-labeled gas mixtures. Important outcomes include: i) identification of competing CO2 chemisorption pathways; ii) effect on CO2 speciation of textural properties, amine type, inter-amine spacing, and amine-support cooperative effects; iii) real-time monitoring of acid gas speciation in multiple adsorption/desorption cycles; iv) identification of sorbent deactivation species; v) effect of pressure on CO2 speciation and vi) improvement of AMPS sorbent properties by synthetic modification.

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