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BSe g

Uy and Drowart [70UY/DRO] determined the enthalpy change of the reaction [Pg.226]

The auxiliary data calculated from estimated molecular parameters for a diatomic molecule are expected to be quite accurate. The uncertainty in the recalculation to the standard temperature of the result for this iso-molecular reaction is anticipated to be moderate compared to the experimental uncertainty. The value for the enthalpy of formation of BSe(g) is therefore adopted [Pg.226]

Binnewies [90BIN] performed a mass spectrometric investigation of the reaetion between solid boron and Se2(g) in the temperature range 1020 to 1220 K. A second law evaluation of the reaction  [Pg.227]

The combination of the reaction entropy at 298.15 K with the entropy of B(cr) in [89COX/WAG] and the selected entropy value of Sc2(g) yields the selected value of the standard entropy  [Pg.227]

The selected value for the enthalpy of formation is obtained by combining the enthalpy of reaction at 298.15 K with the selected enthalpy of formation of Sc2(g) yielding  [Pg.227]


Minerals which are subsurface are therefore visible, however their brightness is diminished (e.g. subsurface marcasite can have a similar BSE image to clay on the surface). [Pg.27]

Excipients used in injectable formulations have to meet several stringent requirements. A positive identification test uniquely applicable to the excipients is required (e.g., infrared spectrophotometry and chromatography). It is important that manufacturers identify and set appropriate limits for impurities. These limits should be based upon appropriate toxicological data, or the limits described in national compendial requirements. Manufacturing processes should be adequately controlled so that the impurities do not exceed such established specifications. Solvents or catalysts used in the excipient production process should be removed to appropriate levels. If naturally derived, excipients should meet endotoxin levels and may require further testing for bovine spongiform encephalopathy (BSE) /... [Pg.271]

Prepare an ink containing 11.2 pi glutaraldehyde, 2 mg BSA and 0.2 mg BSE per gram of 3% (w/v) hydroxyethyl cellulose. This mixture will not have the consistency required of a screen-printing ink. The viscosity should be adjusted by the addition of graphite powder (about 300 mg graphite powder/1 g ink). [Pg.1228]

Gizzi, G., van Raamsdonck, L. W. D., Baeten, V. etal. (2003) An overview of tests for animal tissues in animal feeds used in the public health response against BSE. In Risk Analysis of Prion Diseases in Animals (C. I. Lasmzas and D. B. Adams, eds), Sci. Tech. Rev, 22(1), 311-31. [Pg.300]

When antibodies are from bovine and ovine origin, the possibility of having them contaminated by slow and latent agents such as TDE should be considered (e.g., BSE from bovine extracts, or scrapie from sheep or CJD in man). [Pg.616]

II) PCR-RFLP With Bse 1 a species-specific fragment (e.g. from Helminthosporium solani) containing the mutation was cut [23]. [Pg.79]


See other pages where BSe g is mentioned: [Pg.103]    [Pg.103]    [Pg.226]    [Pg.226]    [Pg.226]    [Pg.226]    [Pg.226]    [Pg.226]    [Pg.640]    [Pg.647]    [Pg.103]    [Pg.103]    [Pg.226]    [Pg.226]    [Pg.226]    [Pg.226]    [Pg.226]    [Pg.226]    [Pg.640]    [Pg.647]    [Pg.1642]    [Pg.456]    [Pg.717]    [Pg.697]    [Pg.213]    [Pg.794]    [Pg.802]    [Pg.108]    [Pg.206]    [Pg.32]    [Pg.138]    [Pg.774]    [Pg.98]    [Pg.396]    [Pg.255]    [Pg.631]    [Pg.295]    [Pg.155]    [Pg.171]    [Pg.301]    [Pg.33]    [Pg.394]    [Pg.6]    [Pg.12]    [Pg.13]    [Pg.24]    [Pg.32]    [Pg.170]    [Pg.552]    [Pg.520]    [Pg.993]   


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