Opendata, web and dolomites

COUPC1 SIGNED

Coupling strategies for scavenging reactive C1 intermediates in hydrogen generation

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 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.

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

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.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "COUPC1" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

The information about "COUPC1" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.3.2.)

EXPAND (2019)

Examining pan-neotropical diasporas

Read More  

qCHROMDEK (2019)

Quantitative insight into chromatin nanoscale structure: sub-nuclear organisation of oncoprotein DEK

Read More  

COSMOS (2020)

The Conformation Of S-phase chroMOSomes

Read More