scholarly journals Communication—Redox Behavior of Cu2S in Li2S-Dissolving Aprotic Electrolyte for Sulfide-Ion Batteries

2020 ◽  
Vol 167 (12) ◽  
pp. 122504
Author(s):  
Ryo Fukunaga ◽  
Antoine Allanore ◽  
Shunsuke Yagi
1997 ◽  
Vol 12 (4) ◽  
pp. 225-229
Author(s):  
Cart-in A-S. Gustavsson ◽  
Chritofer T. Lindgren ◽  
Mikael E. Lindström

Abstract The amount of lignin reacting according to the slow residual phase, i.e. the residual phase lignin, is in many perspectives an interesting issue. The purpose of the present investigation was to develop a mathematical model to show how the amount of residual phase lignin in the kraft cooking of spruce chips (Picm ahies) depends on the conditions in the earlier phases of the cook. The variables studied were hydroxide ion concentration, hydrogen sulfide ion concentration and ionic strength. The liquor-to-wood ratio during pulping was very high to maintain approximately constant chemical concentrations throughout each experiment (so called "constant composition" cooks). An increase in hydroxide ion concentration andtor hydrogen sulfide ion concentration leads to a decrease in the amount of residual phase lignin, while an increase in ionic strength, i.e. sodium ion concentration, leads to an increase. A signiticant result is that the hydrogen sulfide ion concentration has a pronounced influence on the amount of residual phase lignin during a cook at a low hydroxide ion concentration. The amount of residual phase lignin expressed as % lignin on wood, L,, can be described by the following equation developed for "constant composition" cooks (when cooking with a constant sodium ion concentration of 2 mol/L): LT=0,55-0.32*[HO-](-1,3)*ln[HS-] This equation is valid for a concentration of HO- in the range from 0.17 to 1.4, and a hydrogen sulfide ion concentration from 0.07 to 0.6 mol/L.


Author(s):  
So Jeong Park ◽  
Min Hee Joo ◽  
Ju Hyun Yang ◽  
Sung-Min Hong ◽  
Choong Kyun Rhee ◽  
...  
Keyword(s):  

2021 ◽  
Vol 60 (8) ◽  
pp. 6107-6107
Author(s):  
Baihua Chen ◽  
Bijun Liu ◽  
Yao He ◽  
Daibing Luo ◽  
Wanjun Mu ◽  
...  
Keyword(s):  

1987 ◽  
Vol 262 (15) ◽  
pp. 6962-6964
Author(s):  
D N Weber ◽  
C F Shaw ◽  
D H Petering

2021 ◽  
Vol 31 (5) ◽  
pp. 1496-1505
Author(s):  
Liang XU ◽  
Yan-hang XIONG ◽  
Jin-wei MENG ◽  
Jia-bao WANG ◽  
Zhong-sheng HUA ◽  
...  

2019 ◽  
Vol 21 (6) ◽  
pp. 3227-3241 ◽  
Author(s):  
Krishnamoorthy Arumugam ◽  
Neil A. Burton

Of particular interest within the +6 uranium complexes is the linear uranyl(vi) cation and it forms numerous coordination complexes in solution and exhibits incongruent redox behavior depending on coordinating ligands. This DFT study predicts VI/V reduction potentials of a range of uranyl(vi) complexes in non-aqueous solutions within ∼0.10−0.20 eV of experiment.


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