Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Recharge study

Secondary lithium-metal batteries which have a lithium-metal anode are attractive because their energy density is theoretically higher than that of lithium-ion batteries. Lithium-molybdenum disulfide batteries were the world s first secondary cylindrical lithium—metal batteries. However, the batteries were recalled in 1989 because of an overheating defect. Lithium-manganese dioxide batteries are the only secondary cylindrical lithium—metal batteries which are manufactured at present. Lithium-vanadium oxide batteries are being researched and developed. Furthermore, electrolytes, electrolyte additives and lithium surface treatments are being studied to improve safety and recharge-ability. [Pg.57]

Many studies have been undertaken with a view to improving lithium anode performance to obtain a practical cell. This section will describe recent progress in the study of lithium-metal anodes and the cells. Sections 3.2 to 3.7 describe studies on the surface of uncycled lithium and of lithium coupled with electrolytes, methods for measuring the cycling efficiency of lithium, the morphology of deposited lithium, the mechanism of lithium deposition and dissolution, the amount of dead lithium, the improvement of cycling efficiency, and alternatives to the lithium-metal anode. Section 3.8 describes the safety of rechargeable lithium-metal cells. [Pg.340]

With regard to rechargeable cells, a number of laboratory studies have assessed the applicability of the rocking-chair concept to PAN-EC/PC electrolytes with various anode/cathode electrode couples [121-123], Performance studies on cells of the type Li°l PAN-EC/PC-based electrolyte lLiMn20 and carbon I PAN-EC/PC-based electrolyte ILiNi02 show some capacity decline with cycling [121]. For cells with a lithium anode, the capacity decay can be attributed mainly to passivation and loss of lithium by its reaction with... [Pg.516]

The stoichiometry of the recharged DNA/PLL/SPLL particles was studied using sucrose-gradient ultracentrifugation of fluorescently labeled polyion complexes in 25 mM HEPES buffer. Rhodamine-labeled DNA (Rh-DNA) and either fluorescein-labeled PLL (Fl-PLL) or SPLL (Fl-SPLL) were used to determine their relative amounts within DNA... [Pg.450]

Modeling of the transport of the long-lived nuclides, especially U, require knowledge of the input at the water table as a boundary condition for aquifer profiles. There are few studies of the characteristics of radionuclides in vadose zone waters or at the water table. Significant inputs are likely to occur to the aquifer due to elevated rates of weathering in soils, and this is likely to be dependent upon climatic parameters and has varied with time. Soils may also be a source of colloids and so provide an important control on colloidal transport near recharge regions. [Pg.355]

The theoretical models of effects of recharging of the surface on the band diagram in the surface-adjacent domain of semiconductor adsorbent accompanying adsorption have been developed. The effect of the surface band bending in semiconductor adsorbent on its electrophysical characteristics caused by transition phenomena have been studied. The theories of adsorption-caused response of above characteristics were derived for both ideal monocrystalline adsorbent [4] and monocrystal with... [Pg.92]

Adsorption-desorption Partly Mechanisms for adsorption on similar materials will be similar. Soil adsorption data generally do not reflect the saturated conditions of the deep-well environment. Organic-matter content is a major factor affecting adsorption in the near-surface its significance in the deep-well environment is less clear. Fate studies involving artificial recharge are probably useful, but differences between fresh waters and deep brines may reduce relevance. [Pg.793]

Peek, H.M. and Heath, R.C., Feasibility study of liquid-waste injection into aquifers containing salt water, Wilmington, North Carolina, in Symposium on Underground Waste Management and Artificial Recharge, Braunstein, J., Ed., publication 110, International Association of Hydrological Sciences, 1973, pp. 851-875. [Pg.856]

The second and the third papers of this chapter were contributed by Bulgaria s National Academy of Sciences distinguished developers, Dr. A. Kaisheva and Professor I. Iliev. The two papers address magnesium-air and zinc-air chemistries, respectively. Concepts of mechanical recharging, new non-KOH based electrolytes, and the role of carbon materials in cell design have been thoroughly studied. Authors have reduced to practice their many developments. Systems created work(ed) in many specialty applications. [Pg.108]

Chitra, S., Kalyani, P., Vebka, B., Mohan, T., Haro-Poniatowski, E., Gangadharan, R., Julien, C., Synthesis, characterization and electrochemical studies of LiNiVCL cathode material in rechargeable lithium batteries, Mater. Chem. Phys. 65, 32-37 (2000). [Pg.508]

Tritium extracted from soil moisture in the unsaturated zone at various depths below the surface has been used to infer the progress of recharge of underlying aquifers. Studies of recharge in arid and semi arid zones where water moves very slowly in a downward direction have been particularly instructive [20, 32-35]. [Pg.197]

Dincer, T., Al-Mugrin, A., Zimmermann, U., Study of the infiltration and recharge through the sand dunes in arid zones with special reference to the stable isotopes and thermonuclear tritium, J. Hydrology. 23, 79-109 (1974). [Pg.222]


See other pages where Recharge study is mentioned: [Pg.222]    [Pg.346]    [Pg.222]    [Pg.346]    [Pg.7]    [Pg.564]    [Pg.566]    [Pg.300]    [Pg.385]    [Pg.500]    [Pg.2]    [Pg.38]    [Pg.450]    [Pg.452]    [Pg.773]    [Pg.36]    [Pg.322]    [Pg.325]    [Pg.332]    [Pg.117]    [Pg.615]    [Pg.620]    [Pg.804]    [Pg.319]    [Pg.348]    [Pg.408]    [Pg.45]    [Pg.45]    [Pg.566]    [Pg.111]    [Pg.113]    [Pg.148]    [Pg.197]    [Pg.198]    [Pg.395]    [Pg.105]    [Pg.189]    [Pg.215]    [Pg.185]    [Pg.607]    [Pg.636]   
See also in sourсe #XX -- [ Pg.360 ]




SEARCH



Recharge

Rechargeability

© 2024 chempedia.info