Boron Hydrides. VII. The Metal Ion Catalyzed Hydrolysis of Sodium Borohydride in Heavy Water

1964 ◽  
Vol 3 (3) ◽  
pp. 460-461 ◽  
Author(s):  
Robert Earl Davis ◽  
Judith Ann Bloomer ◽  
David R. Cosper ◽  
Afif Saba
1962 ◽  
Vol 84 (6) ◽  
pp. 885-892 ◽  
Author(s):  
Robert Earl. Davis ◽  
Edward. Bromels ◽  
Charles L. Kibby

2021 ◽  
pp. 2000135
Author(s):  
Yan Wang ◽  
Zhe Hu ◽  
WeiHua Chen ◽  
Shiwei Wu ◽  
Guode Li ◽  
...  

2021 ◽  
Vol 19 (1) ◽  
pp. 432-441
Author(s):  
Pawel Jeżowski ◽  
Olivier Crosnier ◽  
Thierry Brousse

Abstract Energy storage is an integral part of the modern world. One of the newest and most interesting concepts is the internal hybridization achieved in metal-ion capacitors. In this study, for the first time we used sodium borohydride (NaBH4) as a sacrificial material for the preparation of next-generation sodium-ion capacitors (NICs). NaBH4 is a material with large irreversible capacity of ca. 700 mA h g−1 at very low extraction potential close to 2.4 vs Na+/Na0. An assembled NIC cell with the composite-positive electrode (activated carbon/NaBH4) and hard carbon as the negative one operates in the voltage range from 2.2 to 3.8 V for 5,000 cycles and retains 92% of its initial capacitance. The presented NIC has good efficiency >98% and energy density of ca. 18 W h kg−1 at power 2 kW kg−1 which is more than the energy (7 W h kg−1 at 2 kW kg−1) of an electrical double-layer capacitor (EDLC) operating at voltage 2.7 V with the equivalent components as in NIC. Tin phosphide (Sn4P3) as a negative electrode allowed the reaching of higher values of the specific energy density 33 W h kg−1 (ca. four times higher than EDLC) at the power density of 2 kW kg−1, with only 1% of capacity loss upon 5,000 cycles and efficiency >99%.


Nature ◽  
1964 ◽  
Vol 204 (4964) ◽  
pp. 1189-1190
Author(s):  
ROBERT W. HAY ◽  
NEIL J. WALKER

1969 ◽  
Vol 47 (22) ◽  
pp. 4199-4206 ◽  
Author(s):  
R. E. Robertson ◽  
B. Rossall ◽  
S. E. Sugamori ◽  
L. Treindl

Rates of solvolysis of methanesulfonyl chloride and benzenesulfonyl chloride have been determined in H2O and D2O. The free energy, enthalpy, entropy, and heat capacity of activation were calculated. The exceptional accuracy of the data permitted an estimation of dΔCp≠/dT from a four parameter temperature dependence of the kinetic rates.From these data we conclude that both sulfonyl chlorides hydrolyse by the same mechanism (Sn2) The change in R from CH3 to C6H5 in RSO2Cl did not alter ΔCp≠ but ΔS≠ (20°) was changed from −8.32 to −13.25 cal deg−1 mole−1, respectively. The significance of this difference is attributed to the probability of bond formation rather than to differences in solvent reorganization.


1964 ◽  
Vol 26 (8) ◽  
pp. 1415-1420 ◽  
Author(s):  
J.M. Rainey ◽  
M.M. Jones ◽  
W.L. Lockhart

2009 ◽  
Vol 34 (5) ◽  
pp. 2153-2163 ◽  
Author(s):  
Cheng-Hong Liu ◽  
Bing-Hung Chen ◽  
Chan-Li Hsueh ◽  
Jie-Ren Ku ◽  
Ming-Shan Jeng ◽  
...  

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