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.

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

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.)

5G-ACE (2019)

Beyond 5G: 3D Network Modelling for THz-based Ultra-Fast Small Cells

Read More  

MNSWLGM (2019)

An optofluidic platform based on liquid-gradient refractive index microlens for the isolation and quantification of extracellular vesicles

Read More  

TheaTheor (2018)

Theorizing the Production of 'Comedia Nueva': The Process of Play Configuration in Spanish Golden Age Theater

Read More