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Lithium formation

Normally, lithium hydride ignites in air only at high temperatures. When heated it reacts vigorously with CO2 and nitrogen. With the former, lithium formate is obtained. Reaction at high temperature with nitrogen produces lithium nitride. Therefore, dry limestone or NaCl powders are used to extinguish LiH fires. Lithium hydride reacts exothermically with moist air and violently with water. [Pg.297]

Among many polar aprotic solvents, including ethers, BL, PC, and ethylene carbonate (EC), methyl formate (MF) seems to be the most reactive towards lithium. It is reduced to lithium formate as a major product which precipitates on the lithium surface and passivates it [24], The presence of trace amounts of the two expected contaminants, water and methanol, in MF solutions does not affect the surface chemistry. C02 in MF causes the formation of a passive film containing both lithium formate and lithium carbonate. [Pg.424]

J. Ji, S. Narayan-Sarathy, R.H. Neilson, J.D. Oxley, D.A. Babb, N.G. Rondon, and W.S. Jr. Smith, [p-( (Trifluorovinyl)oxy)phenyl]lithium formation, synthetic utility, and theoretical support for a versatile new reagent in fluoropolymer chemistry, Organometallics, 17 783-785 (1998). [Pg.399]

Experimentally, x values for gaseous lithium halides were determined as early as 1949 by molecular beam resonance experiments In solution, the quadrupolar interaction of ethyUithium and of t-butyllithium were investigated in 1964 . It was found that tetrameric and hexameric aggregates have different interactions. In the solid state x of tetrameric methyl- and ethyUithium was determined in 1965 and 1966 , and for lithium formate in 1972 . However, it was not untU Jackman started his investigations of lithium enolates and phenoxides in solution that the quadrupolar interaction was used in a systematic fashion to obtain structural information . [Pg.149]

The specific peptide composition can be used to characterize foods. Abe (124) separated the peptides carnosine, anserine, and balenine from the white and red muscle of nine species of marine fishes. Carnegie et al. (37,38) developed an HPLC method using a Partisil-lOSCX column with 0.2 M lithium formate at a pH of 2.9 and a temperature of 40°C under isocratic conditions with postcolumn derivatization using OPA to separate the dipeptides of histidine, anserine, carnosine, and balenine from the muscles of various species (pork, chicken, beef, lamb, and mutton) in order to identify the origin of the meat used in meat products. The concentration of balenine and the balenineranserine ratio were higher in pork than in the other meats, and these relationships were useful in determining the presence of pork in mixtures with other meats. [Pg.117]

Li20 and LiOH are formed on noble metals in these solutions by trace water reduction (in the presence of Li+) below 1.5 V (Li/Li+). In the case of MF, the major constituent of the surface films is lithium formate (HCOOLi) formed... [Pg.170]

ReductUm of aJkenes and aOcynes. Alkenes and alkynes are reduced to alkanes by a mixture of formic acid and lithium formate at 40-60 in the presence of this catalyst. Triphenylphdsphine complexes of ruthenium and iridium are also effective. [Pg.562]

Tsirelson et al. [194] extended Levine s model to account for the different types of bonds in second-order nonlinear susceptibility calculations. Applications to lithium formate deuterate (LiCOOH D2O) and related crystals with and without water molecules showed that the water can play a significant role in X -. They also proposed an expression for X which gave qualitative agreement with experiment for five ionic crystals. [Pg.83]

The presence of sodium on a catalyst also influences its behavior during ethylene polymerization [541,606-608]. When sodium is present, Cr/silica produces its peak activity, and highest MI polymer, after activation at lower temperatures. Other alkali metals can have a similar influence. Figure 141 shows the results of polymerization tests conducted with Cr/silica-titania impregnated with varying levels of sodium formate or lithium formate, followed by activation at 650 °C. The activity of the catalyst and the MI of the polymer it produced pass through a maxima at a loading of about 0.3 Na or Li ions nm-2. [Pg.390]

FIGURE 141 Above Activity of Cr/silica-titania (5 wt% Ti02) catalysts doped with varying amounts of sodium or lithium formate, then activated at 650 °C and tested at 107 °C. Below Melt indices of polymers made with the catalysts described above. [Pg.390]

Hofmann (53) found an appreciable amount of formaldehyde (about 25%) and small amounts of methyl formate during the decomposition of zinc formate. Lithium formate produced acetone (about 20%) from lead formate, formaldehyde and methyl alcohol were formed. Pichler (127) found that during the decomposition of calcium formate, oxalate was formed. In general it appeared that the nature and the amount of the organic by-products depended largely on the reaction conditions [Hofmann (53)]. [Pg.103]

Solubility op Neutral Lithium Formate in Anhydrous Formic Acid. [Pg.174]

Selected bond distances of alkali metal chalcogenocarboxylates are collected in Table 1. The molecular structure of lithium benzoate 2 is a centrosymmetric dimer with an eight-membered ring composed of coplanar C, O, and S atoms and tetrahedrally-coordinated Li atoms above and below this plane, where the C-0 [1.246(2) A] and C-S distances [1.704(2) A] show considerable multiple bond character [6]. From an ab initio optimization calculation on a dimeric lithium formate (HCOSLi)2, the PhCOS unit in 1-2 has been predicted to be predominantly ionic [6]. [Pg.17]

Composition of Lil dissociation products in atmospheric-pressure thermal plasma is shown in Fig. 7-40. The initial concentration of Lil is 7.47 mol/kg. Lithium formation takes place at temperatures exceeding 2500 K. The energy cost of lithium production from iodide is shown inFig. 7 1. The minimal energy cost is 7.44 eV/atom in the case of absolute quenching, and 7.35 eV/atom in the case of ideal quenching, which can be achieved at a specific energy input of 6.7 eV/mol. [Pg.451]


See other pages where Lithium formation is mentioned: [Pg.573]    [Pg.138]    [Pg.436]    [Pg.778]    [Pg.440]    [Pg.332]    [Pg.1263]    [Pg.155]    [Pg.398]    [Pg.398]    [Pg.573]    [Pg.301]    [Pg.881]    [Pg.421]    [Pg.778]    [Pg.281]    [Pg.302]    [Pg.421]    [Pg.909]    [Pg.436]    [Pg.837]    [Pg.857]    [Pg.778]    [Pg.532]    [Pg.126]    [Pg.222]    [Pg.871]    [Pg.155]    [Pg.12]    [Pg.837]    [Pg.722]    [Pg.174]    [Pg.174]    [Pg.714]   
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