Research output: Contribution to journal › Article › peer-review
Non-isothermal kinetics and in situ SR XRD studies of hydrogen desorption from dihydrides of binary Ti–V alloys. / Suwarno, S.; Solberg, J.k.; Mæhlen, J.p.; Denys, R.v.; Krogh, B.; Ochoa-fernández, E.; Børresen, B.t.; Rytter, E.; Gabis, I.e.; Yartys, V.a.
In: International Journal of Hydrogen Energy, Vol. 38, No. 34, 01.11.2013, p. 14704-14714.Research output: Contribution to journal › Article › peer-review
}
TY - JOUR
T1 - Non-isothermal kinetics and in situ SR XRD studies of hydrogen desorption from dihydrides of binary Ti–V alloys
AU - Suwarno, S.
AU - Solberg, J.k.
AU - Mæhlen, J.p.
AU - Denys, R.v.
AU - Krogh, B.
AU - Ochoa-fernández, E.
AU - Børresen, B.t.
AU - Rytter, E.
AU - Gabis, I.e.
AU - Yartys, V.a.
PY - 2013/11/1
Y1 - 2013/11/1
N2 - Phase transformations during dynamic dehydrogenation of Ti(1−x)VxH2 (x = 0.1; 0.2; 0.3) were studied using in situ Synchrotron X-Ray Diffraction (SR XRD) and non-isothermal kinetics experiments. The main dehydrogenation path for γ-Ti(1−x)VxH2 was found to be γ → δ → β → βalloy. Body-centred tetragonal δ-hydride was found to be an intermediate phase of the γ → β transformation in Ti0.8–0.9V0.1–0.2H2. TDS, in situ SR XRD and isoconversional kinetics studies showed that hydrogen desorption from Ti1−xVxH2 is composed of simultaneous reactions taking place between 300 and 600 °C. The effective activation energy of hydrogen desorption depends on the vanadium contents and the reaction pathway, increasing from 21 kJ/mol H2 (γ → δ) to 60–110 kJ/mol H2 (δ → β).
AB - Phase transformations during dynamic dehydrogenation of Ti(1−x)VxH2 (x = 0.1; 0.2; 0.3) were studied using in situ Synchrotron X-Ray Diffraction (SR XRD) and non-isothermal kinetics experiments. The main dehydrogenation path for γ-Ti(1−x)VxH2 was found to be γ → δ → β → βalloy. Body-centred tetragonal δ-hydride was found to be an intermediate phase of the γ → β transformation in Ti0.8–0.9V0.1–0.2H2. TDS, in situ SR XRD and isoconversional kinetics studies showed that hydrogen desorption from Ti1−xVxH2 is composed of simultaneous reactions taking place between 300 and 600 °C. The effective activation energy of hydrogen desorption depends on the vanadium contents and the reaction pathway, increasing from 21 kJ/mol H2 (γ → δ) to 60–110 kJ/mol H2 (δ → β).
KW - Titanium
KW - Vanadium
KW - Metal hydride
KW - In situ synchrotron X-ray diffraction
KW - Thermal desorption spectroscopy
KW - Isoconversional kinetics
U2 - 10.1016/j.ijhydene.2013.08.103
DO - 10.1016/j.ijhydene.2013.08.103
M3 - Article
VL - 38
SP - 14704
EP - 14714
JO - International Journal of Hydrogen Energy
JF - International Journal of Hydrogen Energy
SN - 0360-3199
IS - 34
ER -
ID: 5691546