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Lithium salt solutions

Table 6.8 reports the relative reaction rates of Diels-Alder reactions of 2,5-dimethylbenzoquinone with tran -piperylene in different lithium salt solutions. The data show that the reaction rate depends on the concentration of LT and that in 4.0m LT-AC and 4.0m LT-DE the rate accelerations are comparable to that exhibited in 5.0m LP-DE and 5.0m LP-AC. [Pg.275]

Tadic et al. studied the polymer poly-vynilidene fluoride/hexa-fluoropropylene ( PVdF/HFP ) containing lithium salt solution in Ethylene carbonate/diethylene carbonate ( EC/DEC )- In order to understand better the effect of anion size in the electrolyte, two Li salts were compared, namely LiN(CF3S02)2 (termed Liimide by the authors) and LiN(C2F5S02)2 (termed Libeti ). [Pg.109]

The lithium salt solutions were prepared by adding the chosen salt (LiCl, LiBr, or LiNOj) to the N,N-dimethylacetamide followed by addition of the polysaccharide. Complete dissolution of the polysaccharide required several hours—often with heating and cooling cycles. [Pg.373]

Figure 48. Anodic stability as measured on a spinel LL-Mn204 cathode surface for EMS-based electrolytes (a) Lilm (b) LiC104 (c) LiTf. In all cases, 1.0 m lithium salt solutions were used, and slow scan voltammetry was conducted at 0.1 mV s with lithium as counter and reference electrodes and spinel LiJV[n204 as working electrode. (Reproduced with permission from ref 75 (Figure 3). Copyright 1998 The Electrochemical Society.)... Figure 48. Anodic stability as measured on a spinel LL-Mn204 cathode surface for EMS-based electrolytes (a) Lilm (b) LiC104 (c) LiTf. In all cases, 1.0 m lithium salt solutions were used, and slow scan voltammetry was conducted at 0.1 mV s with lithium as counter and reference electrodes and spinel LiJV[n204 as working electrode. (Reproduced with permission from ref 75 (Figure 3). Copyright 1998 The Electrochemical Society.)...
The conductance of lithium salt solutions in aprotic solvents generally shows a maximum as the concentration of electrolyte is increased, as illustrated in Fig. 4.5. Such maxima can be interpreted on the basis of the opposing influence of an increasing number of charge carriers on the one hand, and increasing viscosity and increasing ion association with the formation of non-conducting ion pairs, on the other. It has been shown that the conductance can be increased by the addition of crown ethers, such as 12-cr own-4 ... [Pg.111]

Since some ILs have excellent electrochemical stability, as shown in Table 3.14, they are favorable for application as electrolyte materials. Recently, ionic liquids have been investigated as conductive and redox media for lithium ions. Stable electrochemical deposition and dissolution of Li metal (Li/Li+) was observed for the lithium salt solution of [Nni3][TFSI], [N 122,201][TFSI], and [PPi4][TFSI] [101-103]. In order to observe the redox couple of lithium metal, Ni should be used as working electrode because it does not form alloys with lithium metal. In addition to this, the atmosphere must be pure Ar, because Li metal reacts rapidly with N2 to form conductive LiN. [Pg.68]

Tetraalkyl ammonium (TAA) salts are characterized by very low reduction potentials, along with good solubility in many organic solvents. Thus, nonaqueous solutions composed of such salts (e.g., tetrabutyl ammonium perchlorate and organic solvents such as ethers, esters, and alkyl carbonates) can be electrolyzed using noble metal electrodes. In contrast to lithium salt solutions, in TAA-based solutions there is no precipitation of insoluble products on the electrode, which leads to its passivation. Therefore, it is possible to isolate and identify the electrolysis products and thus outline precise reduction mechanisms for the various systems. [Pg.148]

Figure 8 Typical voltammograms obtained from lithium salt solutions of BL with gold... [Pg.163]

The potassium salt is a white crystalline powder, more soluble in lithium salt solutions than in pure water. The solution is not stable Moderate acidification leads to a mixtureof [a,-P2Wn08,] and [P8W480,84] anions. The half-wave potentials (V vs SCE) in molar acetic acid-lithium acetate buffer are - 0.59 (2e) and —0.69 (2c). The PNMR spectrum of a freshly prepared solution in lithium chloride exhibits a single resonance at -8.6ppm. In the IR spectrum, the P—O bands are at 1130, 1075, and 1012 cm" (KBr pellet). [Pg.109]

Of the results obtained over the past few years, those for hexamethylphosphotriamide are most interesting. For lithium salt solutions the shape of anodic curves conforms to oxidation of particles of only one type. This is in accord with the results of the studies on the state of solvated electrons in these systems. Indeed, as shown in Section 4, in the presence of a lithium salt the electrons exist exclusively as monoelectrons e part of these electrons, when the salt is in excess, can be bound into noncontact ion pairs with lithium cations. The electrons in these pairs differ only slightly in their properties from non-associated electrons. And this yields a singlewave anodic curve. [Pg.180]

The anodic limiting current in lithium salt solutions is determined by the diffusion of the solvated electrons to the electrode. This was quantitatively established by the measurements taken on rotating disc electrodes and also by galvanostatic measurements In fact, as seen from Fig. 8, the limiting current density is proportional to the square root of the disc electrode rotation rate. This, in accordance with the rotat-... [Pg.180]

High-energy batteries with a lithium anode are classified < with regard to the type of their ionic conductor. This can be a fast solid Li -ion conductor, a fused lithium salt, a lithium-potassium-salt eutectic mixture, or a non-aqueous lithium salt solution. If inorganic solvents are used, e.g. SOj, SOClj, SOjClj, the solvent itself is the depolarizer and then a solid catalytic electrode is needed, e.g. carbon. The type of ionic conductor determines the internal resistance of the cell and the working temperature range and hence the possible technical applications. [Pg.86]

III. VOLTAMMETRIC BEHAVIOR OF LITHIUM SALT SOLUTIONS IN ETHERS, ESTERS AND ALKYL CARBONATES... [Pg.154]

The SCC behavior of cold worked AISI type 316L (UNS S31603) stainless steel in a concentrated lithium salt solution at elevated temperature was investigated by Zheng and Bogaerts [138]. Using the SSRT technique, SCC experiments were performed under controlled electrochemical potential on 20% and 40% cold worked materials in a solution... [Pg.406]

Ryu Y.-G., Lee S., Mah S., Lee D. J., Kwon K., Hwang S., Doo S. Electrochemical Behaviors of Silicon Electrode in Lithium Salt Solution Containing Alkoxy Silane Additives, J. Electrochem. Soc. 2008, 155, A583-A589. [Pg.356]

Monteiro MJ, Bazito EEC, Siqueira LJA, Ribeiro MCC, Toiresi RM (2008) Transport coefficients, Raman spectroscopy, and computer simulation of lithium salt solutions in an ionic liquid. J Phys (Them B 112 2102... [Pg.238]

Some commercial preparations of GTP contain a significant amount of GDP, which competes with GTP during the nucleotide-loading step. Therefore, GTP and analogues should be of the highest purity available. We use lithium salt solutions of nucleotides from Roche (www.roche-diagnostics. com). [Pg.96]

Figure 3. Dependence of the transformation degree (a) of Al(OH)3 into LADH-X on concentration of lithium salt solution (M/1 Li). - -LiCl, - 3 - LiN03, ——Li2S04, —A— LiBr. Time of treatment Ihour for LiCl, LiBr and LiN03 2 hours for Li2S04. T-363K. Figure 3. Dependence of the transformation degree (a) of Al(OH)3 into LADH-X on concentration of lithium salt solution (M/1 Li). - -LiCl, - 3 - LiN03, ——Li2S04, —A— LiBr. Time of treatment Ihour for LiCl, LiBr and LiN03 2 hours for Li2S04. T-363K.
Table 1.9 Common lithium salts (solutes) in lithium-ion electrolyte... Table 1.9 Common lithium salts (solutes) in lithium-ion electrolyte...

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