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  2. Prism correction - Wikipedia

    en.wikipedia.org/wiki/Prism_correction

    Thus a prism of 1 Δ would produce 1 cm visible displacement at 100 cm, or 1 meter. This can be represented mathematically as: = ⁡ where is the amount of prism correction in prism dioptres, and is the angle of deviation of the light.

  3. Electron energy loss spectroscopy - Wikipedia

    en.wikipedia.org/wiki/Electron_energy_loss...

    Experimental electron energy loss spectrum, showing the major features: zero-loss peak, plasmon peaks and core loss edge. Electron energy loss spectroscopy ( EELS) is a form of electron microscopy in which a material is exposed to a beam of electrons with a known, narrow range of kinetic energies. Some of the electrons will undergo inelastic ...

  4. Volume correction factor - Wikipedia

    en.wikipedia.org/wiki/Volume_Correction_Factor

    Formula and usage The formula for Volume Correction Factor is commonly defined as: V C F = C T L = exp ⁡ { − α T Δ T [ 1 + 0.8 α T ( Δ T + δ T ) ] } {\displaystyle VCF=C_{TL}=\exp\{-\alpha _{T}\Delta T[1+0.8\alpha _{T}(\Delta T+\delta _{T})]\}}

  5. Atomic absorption spectroscopy - Wikipedia

    en.wikipedia.org/wiki/Atomic_absorption_spectroscopy

    Atomic absorption spectroscopy ( AAS) and atomic emission spectroscopy ( AES) is a spectroanalytical procedure for the quantitative determination of chemical elements by free atoms in the gaseous state. Atomic absorption spectroscopy is based on absorption of light by free metallic ions. In analytical chemistry the technique is used for ...

  6. Compressibility factor - Wikipedia

    en.wikipedia.org/wiki/Compressibility_factor

    Compressibility factor values are usually obtained by calculation from equations of state (EOS), such as the virial equation which take compound-specific empirical constants as input.

  7. Arrhenius equation - Wikipedia

    en.wikipedia.org/wiki/Arrhenius_equation

    In physical chemistry, the Arrhenius equation is a formula for the temperature dependence of reaction rates.The equation was proposed by Svante Arrhenius in 1889, based on the work of Dutch chemist Jacobus Henricus van 't Hoff who had noted in 1884 that the van 't Hoff equation for the temperature dependence of equilibrium constants suggests such a formula for the rates of both forward and ...

  8. Fugacity - Wikipedia

    en.wikipedia.org/wiki/Fugacity

    For a gas obeying the van der Waals equation, the explicit formula for the fugacity coefficient is R T ln ⁡ φ = R T b V m − b − 2 a V m − R T ln ⁡ ( 1 − a ( V m − b ) R T V m 2 ) {\displaystyle RT\ln \varphi ={\frac {RTb}{V_{\mathrm {m} }-b}}-{\frac {2a}{V_{\mathrm {m} }}}-RT\ln \left(1-{\frac {a(V_{\mathrm {m} }-b)}{RTV_{\mathrm ...

  9. Specific rotation - Wikipedia

    en.wikipedia.org/wiki/Specific_rotation

    In this case, a correction factor in the numerator is necessary:: 248 : 123 [ α ] λ T = 100 × α l × c {\displaystyle [\alpha ]_{\lambda }^{T}={\frac {100\times \alpha }{l\times c}}} When using this equation, the concentration and the solvent may be provided in parentheses after the rotation.

  10. Activity coefficient - Wikipedia

    en.wikipedia.org/wiki/Activity_coefficient

    The ionic activity coefficient is connected to the ionic diameter by the formula obtained from Debye–Hückel theory of electrolytes: log ⁡ ( γ i ) = − A z i 2 I 1 + B a I {\displaystyle \log(\gamma _{i})=-{\frac {Az_{i}^{2}{\sqrt {I}}}{1+Ba{\sqrt {I}}}}}

  11. Nernst equation - Wikipedia

    en.wikipedia.org/wiki/Nernst_equation

    The Nernst equation allows the calculation of the extent of reaction between two redox systems and can be used, for example, to assess whether a particular reaction will go to completion or not. At chemical equilibrium, the electromotive forces (emf) of the two half cells are equal.