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MesoSi-CO2 SIGNED

Design of low-cost and carbon-resistant Ni-based mesoporous silicas for chemical CO2 utilization through tri-reforming of methane

Total Cost €

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EC-Contrib. €

0

Partnership

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 MesoSi-CO2 project word cloud

Explore the words cloud of the MesoSi-CO2 project. It provides you a very rough idea of what is the project "MesoSi-CO2" about.

nature    waste    zero    isotopic    bio    selectivity    synthesis    sites    power    mechanisms    optimal    dft    kinetic    methane    operate    lack    ratios    mesoporous    dioxide    co    tpr    materials    universit    co2    superior    perform    deactivation    performed    led    ssitka    assistance    france    temperature    global    plants    functional    sintering    resistant    tremendous    steady    operando    ni    tga    increasing    effect    eacute    catalytic    experiments    catalysts    gas    sorbonne    atmosphere    flue    fired    advantage    carbon    xrd    physico    eliminate    theory    reactions    stability    conversion    reforming    serious    secondment    h2    composition    reveal    sources    microwaves    natural    xps    industrial    evident    dsc    sufficient    tri    trm    hinders    density    emissions    n2    silica    gases    active    chemical    sorption    greenhouse    takes    ms    converting    solution    examine    latter    stay    desired    renewable    xas    concentrations    plant    transient    technologies    reduce    chemisorption   

Project "MesoSi-CO2" data sheet

The following table provides information about the project.

Coordinator
NORGES TEKNISK-NATURVITENSKAPELIGE UNIVERSITET NTNU 

Organization address
address: HOGSKOLERINGEN 1
city: TRONDHEIM
postcode: 7491
website: www.ntnu.no

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 Norway [NO]
 Total cost 202˙158 €
 EC max contribution 202˙158 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2019
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2020
 Duration (year-month-day) from 2020-10-01   to  2022-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    NORGES TEKNISK-NATURVITENSKAPELIGE UNIVERSITET NTNU NO (TRONDHEIM) coordinator 202˙158.00

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 Project objective

Increasing carbon dioxide (CO2) concentrations in our atmosphere are becoming evident and are having a tremendous effect on the global temperature rise. Growing awareness of greenhouse gas emissions has led to the implementation of chemical CO2 utilization technologies. Tri-reforming of methane (TRM) can not only produce synthesis gas (CO H2) with desired H2/CO ratios (1.5–2.0) but can also eliminate carbon formation which is a serious problem in reforming of methane. Moreover, TRM allows converting CO2 directly from flue gases when applied in natural gas-fired power plants. However, a lack of catalysts able to operate efficiently with sufficient long-term stability hinders the development of the process. In this project, the proposed solution is to design a Ni-based mesoporous silica resistant to sintering and carbon formation and able to perform superior catalytic conversion of CO2. The synthesis of catalysts takes advantage of renewable bio-sources, zero-cost industrial waste and assistance of microwaves. The latter is applied to reduce power usage. The catalytic measurements will be performed with gas composition typical of flue gases from a natural-gas-fired power plant. The materials will be characterized by methods dedicated to examine physico-chemical features, such as XRD, N2 sorption, TPR, H2 chemisorption, TGA/DSC-MS, and XPS. The catalysts with optimal properties will be studied by steady-state isotopic transient kinetic analysis (SSITKA). Moreover, density functional theory (DFT) will be carried out to support the experiments. The understanding of possible deactivation mechanisms (carbon formation, sintering, selectivity towards side reactions) will be studied during the Secondment stay (Sorbonne Université, France). Operando XAS-XRD measurements will be performed to reveal the nature of active sites on the tri-reforming catalysts.

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