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Ions/ionization carbonate

Thus, either the emitted light or the ions formed can be used to examine samples. For example, the mass spectrometric ionization technique of atmospheric-pressure chemical ionization (APCI) utilizes a corona discharge to enhance the number of ions formed. Carbon arc discharges have been used to generate ions of otherwise analytically intractable inorganic substances, with the ions being examined by mass spectrometry. [Pg.388]

To complete the deionization process, water from the cation unit is passed through a strong base anion exchange resin in the hydroxide form. The resin exchanges hydrogen ions for both highly ionized mineral ions and the more weakly ionized carbonic and silicic acids according to1,2 ... [Pg.467]

Flame ionization (FID) Generation of ions from carbon in flame 1 pg/s 6 Carbon containing compounds... [Pg.474]

Diels-alder adducts at 0°C. This cation radical-vinylcyclobutane rearrangement is non-stereospecific, thus accounting for the formation of a cis-trans mixture of Diels-Alder adducts. Kinetic studies revealed (Scheme 8) that the ionization of these ethers involves an inner-sphere electron-transfer mechanism involving strong covalent (electrophilic) attachment to the substrate via oxygen (oxonium ion) or carbon (carbocation). [Pg.182]

Synthetic applications of the /1-pathway include conversions of the TIPS allylic azides to enones with tetrabutylammonium fluoride, ionization of the C-N3 bond with alkylaluminum reagents and capture of the TIPS enonium ions with carbon nucleophiles, and development of a procedure for y-lactamization [15-17]. Allylic azidonations of TIPS enol ethers have also been incorporated into syntheses of (+)-pancratistatin [18,19] and the core structure of lycorane [20]. [Pg.140]

It may be speculated that C60Hf, is best represented by structure 15. It is noteworthy that the formation of fullerene ions from acetylenic 14 is observed in the negative ion mode, which is considered to be milder than the positive ion mode which was previously used to detect ionized carbon spheres. It thus appears that 14 is structurally predisposed for fullerene formation. However, attempts to perform the exhaustive decarbonylation on a macroscopic scale by irradiating dilute THF solutions of 14 with pulsed laser light did not lead to the formation of buckminsterfullerene C6o-... [Pg.415]

Fig. 7. Different estimation of the mean charge state of ions in carbon foils. The lines indicated ND and SG show the empirical fitting expressions for the average charge state of ions crossing solid foils given by Nikolaev-Dmitriev [55] and Schiwietz-Grande [56], respectively. The line BK is the Brandt-Kitagawa model [15] for the equilibrium charge of ions moving inside solids. The line ZBL is the equilibrium ionization value proposed by Ziegler et al. [9]. Fig. 7. Different estimation of the mean charge state of ions in carbon foils. The lines indicated ND and SG show the empirical fitting expressions for the average charge state of ions crossing solid foils given by Nikolaev-Dmitriev [55] and Schiwietz-Grande [56], respectively. The line BK is the Brandt-Kitagawa model [15] for the equilibrium charge of ions moving inside solids. The line ZBL is the equilibrium ionization value proposed by Ziegler et al. [9].
THAM, available as a 0.3 N solution, is a highly alkaline, sodium-free organic amine that acts as a proton acceptor to prevent or correct acidosis. Tromethamine combines with hydrogen ions from carbonic acid to form bicarbonate and a cationic buffer. THAM also acts as an osmotic diuretic to increase urine flow, urine pH, and the excretion of fixed acids, CO2, and electrolytes. At pH 7.4, 30% of THAM is not ionized and therefore may penetrate into cells and neutralize acidic anions of the intracellular fluid. Intracellular pH increases have been noted within 1 hour after the infusion of THAM. There is, however, no chnical or physiologic evidence that this action is beneficial, or that THAM is more efficacious than sodium bicarbonate. " ... [Pg.992]

Some vinyl compounds can function as donor molecules because they possess a low ionization potential. The acceptors can be neutral molecules, like quinones, anhydrides, nitrile compounds, etc. They can also be ionic intermediates, such as metal ions, ionized acids, and carbon cations. An interaction of an acceptor with a donor is followed by a subsequent collapse of the charge transfer complex. This can result in formation of cation radicals capable of initiating cationic polymerizations. The exact mechanism of the reaction of cation radicals with olefins is still not completely determined. [Pg.92]

Li X, Pignatello JJ, Wang Y, Xing B (2013e) New insight into adsorption mechanism of ionizable compounds on carbon nanotubes. Environ Sci Technol 47(15) 8334-8341 Li J, Chen C, Zhang S, Ren X, Tan X, Wang X (2014) Critical evaluation of adsorption-desorption hysteresis of heavy metal ions from carbon nanotubes Influence of wall number and surface functionalization. Chem Asian J 9(4) 1144—1151... [Pg.202]

FIGURE 6.6 (a) The 2D mobility-mass spectrum of 70 eV electron ionized carbon tetrachloride. (b) Mobility spectra for three selected ions, CCP (47 m/z), CClj (82 m/z), and CClj (117 m/z), taken at two different drift gas temperatures (298 and 103 K). At lower temperatures the mobility peaks narrow, leading to an increase in the analytical resolving power (denoted as R in b). Mobility spectra are extracted from the 2D data by integrating the ion current across an m/z window. [Pg.147]

With a weakly ionized acid, such as carbonic acid, the large concentration of dissolved, but un-ionized carbon dioxide in the water provides a reservoir of reactive molecules, which can produce additional hydrogen ions by reaction 3-4 to replace those used up by the corrosion reaction. With a strongly ionized acid, on the other hand, an extremely low acid concentration is needed to produce the same pH as the carbonic acid solution, and depletion of hydrogen ions at the corroding surface can reduce the corrosion rate. Such an effect may explain the higher rates of corrosion observed for CO2 solutions than for strong acid solutions at the same bulk solution pH values (Berry, 1982). [Pg.191]


See other pages where Ions/ionization carbonate is mentioned: [Pg.59]    [Pg.66]    [Pg.199]    [Pg.9]    [Pg.120]    [Pg.204]    [Pg.449]    [Pg.71]    [Pg.337]    [Pg.384]    [Pg.35]    [Pg.197]    [Pg.344]    [Pg.549]    [Pg.9]    [Pg.351]    [Pg.9]    [Pg.181]    [Pg.549]    [Pg.32]    [Pg.1114]    [Pg.996]    [Pg.1121]    [Pg.193]    [Pg.512]    [Pg.1134]    [Pg.141]    [Pg.214]    [Pg.365]    [Pg.365]    [Pg.998]    [Pg.1105]   
See also in sourсe #XX -- [ Pg.51 , Pg.52 ]

See also in sourсe #XX -- [ Pg.51 , Pg.52 ]




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Ions/ionization

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