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NMR4CO2 SIGNED

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

Total Cost €

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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.

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

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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