Big Chemical Encyclopedia

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

Articles Figures Tables About

Cobalt absorption studies

On photolyzing CoziCOg in the matrix (20), a number of photoproducts could be observed. The results of these experiments are summarized in Scheme 4, which illustrates the various species formed. Of particular interest is the formation of Co2(CO)7 on irradiation of Co2(CO)g in CO (254 nm), as this species had not been characterized in the metal-atom study of Hanlan et al. (129). Passage of Co2(CO)g over an active, cobalt-metal surface before matrix isolation causes complete decomposition. On using a less active catalyst, the IR spectrum of Co(CO)4 could be observed. An absorption due to a second decomposition product, possibly Co2(CO)g, was also noted. [Pg.134]

Tominaga et al. [682,683] studied the effect of ascorbic acid on the response of these metals in seawater obtained by graphite-furnace atomic absorption spectrometry from standpoint of variation of peak times and the sensitivity. Matrix interferences from seawater in the determination of lead, magnesium, vanadium, and molybdenum were suppressed by addition of 10% (w/v) ascorbic acid solution to the sample in the furnace. Matrix effects on the determination of cobalt and copper could not be removed in this way. These workers propose a direct method for the determination of lead, manganese, vanadium, and molybdenum in seawater. [Pg.246]

Advantages High analysis rate 3-4 elements per hour Applicable to many more metals than voltammetric methods Superior to voltammetry for mercury and arsenic particularly in ultratrace range Disadvantages Nonspecific absorption Spectral interferences Element losses by molecular distillation before atomisation Limited dynamic range Contamination sensitivity Element specific (or one element per run) Not suitable for speciation studies in seawater Prior separation of sea salts from metals required Suspended particulates need prior digestion About three times as expensive as voltammetric equipment Inferior to voltammetry for cobalt and nickel... [Pg.266]

Perez-Pina et al. [805] studied the use of triethanolamine and dimethyl-glyoxime complexing agents in absorptive cathodic stripping voltammetry of cobalt and nickel in seawater. Nickel and cobalt could be determined at levels down to 2 nM and 50 pM, respectively. [Pg.277]

Most hydroformylation investigations reported since 1960 have involved trialkyl or triarylphosphine complexes of cobalt and, more recently, of rhodium. Infrared studies of phosphine complex catalysts under reaction conditions as well as simple metal carbonyl systems have provided substantial information about the postulated mechanisms. Spectra of a cobalt 1-octene system at 250 atm pressure and 150°C (21) contained absorptions characteristic for the acyl intermediate C8H17COCo(CO)4 (2103 and 2002 cm-1) and Co2(CO)8. The amount of acyl species present under these steady-state conditions increased with a change in the CO/ H2 ratio in the order 3/1 > 1/1 > 1/3. This suggests that for this system under these conditions, hydrogenolysis of the acyl cobalt species is a rate-determining step. [Pg.6]

X-Ray Absorption Fine Structure, Mossbauer, and Reactivity Studies of Unsupported Cobalt-Molybdenum Hydrotreating Catalysts... [Pg.75]

Mossbauer Measurements. Co-Mo catalysts cannot be studied directly in absorption experiments since neither cobalt nor molybdenum has suitable Mossbauer isotopes. However, by doping with 57Co the catalysts can be studied by carrying out Mossbauer emission spectroscopy (MES) experiments. In this case information about the cobalt atoms is obtained by studying the 57Fe atoms produced by the decay of 57Co. The possibilities and limitations on the use of the MES technique for the study of Co-Mo catalysts have recently been discussed (8., 25.). [Pg.78]

The application of electrospray ionization (ESI) to macromolecules was first described by Yamashita and Fenn in 1984, and he later applied this technique to the study of proteins in 1988. In ESI, charged droplets of protein were produced and the solvent was stripped away, leaving only the free protein ion. In 1987, Tanaka demonstrated that laser pnlses from a low-energy nitrogen laser could be used to ionize proteins from a surface. As described in a paper presented during the Second Japan-China Joint Symposium on Mass Spectrometry, proteins are desorbed from a glycerol matrix containing cobalt powder. The cobalt powder was necessary to increase absorption of the laser photons. ... [Pg.500]


See other pages where Cobalt absorption studies is mentioned: [Pg.122]    [Pg.78]    [Pg.289]    [Pg.284]    [Pg.5132]    [Pg.5131]    [Pg.207]    [Pg.289]    [Pg.278]    [Pg.171]    [Pg.98]    [Pg.546]    [Pg.205]    [Pg.12]    [Pg.12]    [Pg.35]    [Pg.416]    [Pg.54]    [Pg.80]    [Pg.295]    [Pg.60]    [Pg.24]    [Pg.125]    [Pg.33]    [Pg.246]    [Pg.259]    [Pg.30]    [Pg.355]    [Pg.252]    [Pg.280]    [Pg.182]    [Pg.309]    [Pg.422]    [Pg.381]    [Pg.309]    [Pg.14]    [Pg.273]    [Pg.102]    [Pg.109]    [Pg.296]    [Pg.494]   
See also in sourсe #XX -- [ Pg.331 , Pg.332 ]




SEARCH



Absorption studies

© 2024 chempedia.info