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In chemistry, the molar absorption coefficient or molar attenuation coefficient (ε) [1] is a measurement of how strongly a chemical species absorbs, and thereby attenuates, light at a given wavelength. It is an intrinsic property of the species.
Bovine serum albumin (BSA or "Fraction V") is a serum albumin protein derived from cows. It is often used as a protein concentration standard in lab experiments. The nickname "Fraction V" refers to albumin being the fifth fraction of the original Edwin Cohn purification methodology that made use of differential solubility characteristics of plasma proteins.
The Molar attenuation coefficient (also called "molar absorptivity"), which is the absorption coefficient divided by molarity (see also Beer–Lambert law) The mass attenuation coefficient (also called "mass extinction coefficient"), which is the absorption coefficient divided by density; The absorption cross section and scattering cross ...
ε is the molar attenuation coefficient of that material, and; c(z) is the molar concentration of that material at z. If c(z) is uniform along the path, the relation becomes =. The use of the term "molar absorptivity" for molar attenuation coefficient is discouraged. [1]
absorption coefficient is essentially (but not quite always) synonymous with attenuation coefficient; see attenuation coefficient for details; molar absorption coefficient or molar extinction coefficient , also called molar absorptivity , is the attenuation coefficient divided by molarity (and usually multiplied by ln(10), i.e., decadic); see ...
Variable pathlength absorption spectroscopy uses a determined slope to calculate concentration. As stated above this is a product of the molar absorptivity and the concentration. Since the actual absorbance value is taken at many data points at equal intervals, background subtraction is generally unnecessary.
Spectral hemispherical attenuation coefficient: μ ν μ λ: m −1: Spectral radiant flux absorbed and scattered by a volume per unit length, divided by that received by that volume. Directional attenuation coefficient: μ Ω: m −1: Radiance absorbed and scattered by a volume per unit length, divided by that received by that volume.
When an isosbestic plot is constructed by the superposition of the absorption spectra of two species (whether by using molar absorptivity for the representation, or by using absorbance and keeping the same molar concentration for both species), the isosbestic point corresponds to a wavelength at which these spectra cross each other.