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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.

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

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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