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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.

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