Hydrogen storage in TiVCrMo and TiZrNbHf multiprinciple-element alloys and their catalytic effect upon hydrogen storage in Mg

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68081723%3A_____%2F22%3A00562085" target="_blank" >RIV/68081723:_____/22:00562085 - isvavai.cz</a>

Výsledek na webu

<a href="https://www.sciencedirect.com/science/article/pii/S0960148122001616?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0960148122001616?via%3Dihub</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.renene.2022.02.021" target="_blank" >10.1016/j.renene.2022.02.021</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Hydrogen storage in TiVCrMo and TiZrNbHf multiprinciple-element alloys and their catalytic effect upon hydrogen storage in Mg

Popis výsledku v původním jazyce

Hydrogen storage performance of nearly equimolar alloys TiVCrMo and TiZrNbH (HEA's) was studied. The alloys were prepared by repeated arc-melting in the form of single-phase alloys and as their multi-phase analogues prepared either by high-energy ball milling (HEBM) of the arc-melted ingots or by HEBM of pure elements. Besides these four-component experimental materials, also their mixtures with Mg were investigated that were prepared by HEBM with Mg (composition in both cases was Mg – 10 wt % HEA). Hydrogen sorption experiments were carried out in temperature interval between 240 °C and 380 °C under hydrogen-gas pressure up to 50 bars. Kinetic curves, temperature-programmed desorption spectra and concentration-pressure isotherms were measured. It was found that activation energy of hydrogen desorption, |Ea|, for materials with Mg was significantly decreased compared to pure Mg. Hydride formation enthalpy, ΔH, observed for all the materials under study was about the same as that for pure MgH2. Hydrogen absorption capacity in pure four-component HEA's was negligible, only hydrogen surface adsorption was detected. The capacity of mixtures of HEA's with Mg was between 3.5 and 6 wt % H2.

Název v anglickém jazyce

Hydrogen storage in TiVCrMo and TiZrNbHf multiprinciple-element alloys and their catalytic effect upon hydrogen storage in Mg

Popis výsledku anglicky

Hydrogen storage performance of nearly equimolar alloys TiVCrMo and TiZrNbH (HEA's) was studied. The alloys were prepared by repeated arc-melting in the form of single-phase alloys and as their multi-phase analogues prepared either by high-energy ball milling (HEBM) of the arc-melted ingots or by HEBM of pure elements. Besides these four-component experimental materials, also their mixtures with Mg were investigated that were prepared by HEBM with Mg (composition in both cases was Mg – 10 wt % HEA). Hydrogen sorption experiments were carried out in temperature interval between 240 °C and 380 °C under hydrogen-gas pressure up to 50 bars. Kinetic curves, temperature-programmed desorption spectra and concentration-pressure isotherms were measured. It was found that activation energy of hydrogen desorption, |Ea|, for materials with Mg was significantly decreased compared to pure Mg. Hydride formation enthalpy, ΔH, observed for all the materials under study was about the same as that for pure MgH2. Hydrogen absorption capacity in pure four-component HEA's was negligible, only hydrogen surface adsorption was detected. The capacity of mixtures of HEA's with Mg was between 3.5 and 6 wt % H2.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

20501 - Materials engineering

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2022

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Renewable Energy

ISSN

0960-1481

e-ISSN

1879-0682

Svazek periodika

188

Číslo periodika v rámci svazku

APR

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

14

Strana od-do

411-424

Kód UT WoS článku

000780024400008

EID výsledku v databázi Scopus

2-s2.0-85124996290