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COUPC1 SIGNED

Coupling strategies for scavenging reactive C1 intermediates in hydrogen generation

Total Cost €

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EC-Contrib. €

0

Partnership

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 COUPC1 project word cloud

Explore the words cloud of the COUPC1 project. It provides you a very rough idea of what is the project "COUPC1" about.

reactive    notable    university    diffusion    dehydrogenates    dehydrogenation    h2    molecules    details    reverse    c1    gonz    microreverse    microscopic    formed    biogenic    supervision    worldwide    hydrogenation    interfacial    shuttle    intermediate    hcooh    positioning    reaction    de    permit    selectively    iglesia    water    lez    selective    intermediates    promotional    requiring    shift    cu    metals    precise    prof    carrier    gas    formic    unstable    researcher    velasco    summarizing    tio2    feedstocks    methanol    turnover    recent    basque    dehydrate    berkeley    routes    mediated    zno    suggested    bond    pt    subsequent    thermodynamically    torre    function    acid    return    forms    country    usa    reactants    mechanistic    co    involvement    completing    uc    distances    unveil    pd    contact    group    catalyst    co2    enrique    detected    au    channelling    aacute    la    molecular    spain    seconded    lsac    natural    promoted    situ    dehydration    wgs    effect    mixtures    oxides    close    scavenging    catalyze    h2o    functions    gaseous    ceo2    plausible    atomic   

Project "COUPC1" data sheet

The following table provides information about the project.

Coordinator
UNIVERSIDAD DEL PAIS VASCO/ EUSKAL HERRIKO UNIBERTSITATEA 

Organization address
address: BARRIO SARRIENA S N
city: LEIOA
postcode: 48940
website: www.ehu.es

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 Spain [ES]
 Total cost 204˙415 €
 EC max contribution 204˙415 € (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-GF
 Starting year 2020
 Duration (year-month-day) from 2020-04-01   to  2022-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSIDAD DEL PAIS VASCO/ EUSKAL HERRIKO UNIBERTSITATEA ES (LEIOA) coordinator 204˙415.00
2    THE REGENTS OF THE UNIVERSITY OF CALIFORNIA US (OAKLAND CA) partner 0.00

Map

 Project objective

Recent findings have suggested the plausible involvement of formic acid (HCOOH) as a gaseous molecular shuttle in WGS reaction , which is specifically promoted by oxides (ZnO, CeO2, TiO2) that are known to selectively dehydrate HCOOH (microreverse of HCOOH formation from CO and H2O) and metals (Cu, Pt, Pd, Au) that do dehydrogenation (to CO2 and H2 in WGS) and hydrogenation (to methanol). The intermediate of interest (HCOOH) is formed in situ from CO/H2O mixtures on metals and oxides that catalyze selective HCOOH dehydration, and thus its microscopic reverse. Subsequent HCOOH dehydrogenation would lead to the formation of H2 and CO2, completing a water-gas shift (WGS ) turnover without requiring interfacial contact among functions. A notable promotional effect has been recently detected in catalyst without requiring atomic contact, meaning that the two functions need to be “close” but not in atomic contact but involving a molecular carrier. The mechanistic details of such diffusion-mediated routes would unveil new opportunities for the specific channelling of such intermediates towards H2 and CO2, through precise positioning of a function that forms HCOOH from CO/H2O reactants and another function, present beyond atomic contact but within diffusion distances, that dehydrogenates gaseous HCOOH to H2 and CO2. Summarizing, this research would permit controlling the WGS process in order to increase H2 production worldwide. The proposed research will address the formation and scavenging of reactive and thermodynamically unstable intermediates without a C-C bond, which can be formed from C1 molecules (specifically natural gas or biogenic feedstocks), through the precise positioning for their formation and scavenging functions. The researcher U. De La Torre will be seconded to the LSAC group at UC Berkeley (USA) under the supervision of Prof. Enrique Iglesia, and will return to the University of the Basque Country (Spain) under the supervision of Prof. González-Velasco.

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