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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.
The concentration of sites is given by dividing the total number of sites (S 0) covering the whole surface by the area of the adsorbent (a): [ S 0 ] = S 0 / a . {\displaystyle [S_{0}]=S_{0}/a.} We can then calculate the concentration of all sites by summing the concentration of free sites [ S ] and occupied sites:
In practice, the drug concentration is measured at certain discrete points in time and the trapezoidal rule is used to estimate AUC. In pharmacology, the area under the plot of plasma concentration of a drug versus time after dosage (called “area under the curve” or AUC) gives insight into the extent of exposure to a drug and its clearance ...
In essence, the Beer Lambert Law makes it possible to relate the amount of light absorbed to the concentration of the absorbing molecule. The following absorbance units to nucleic acid concentration conversion factors are used to convert OD to concentration of unknown nucleic acid samples: [5] A260 dsDNA = 50 μg/mL A260 ssDNA = 33 μg/mL
The absorption coefficient is fundamentally the product of a quantity of absorbers per unit volume, [cm −3], times an efficiency of absorption (area/absorber, [cm 2]). Several sources [ 2 ] [ 12 ] [ 3 ] replace nσ λ with k λ r , where k λ is the absorption coefficient per unit density and r is the density of the gas.
The amount concentration c is then given by = (). For a more complicated example, consider a mixture in solution containing two species at amount concentrations c 1 and c 2 . The decadic attenuation coefficient at any wavelength λ is, given by μ 10 ( λ ) = ε 1 ( λ ) c 1 + ε 2 ( λ ) c 2 . {\displaystyle \mu _{10}(\lambda )=\varepsilon _{1 ...
Absorbance is defined as "the logarithm of the ratio of incident to transmitted radiant power through a sample (excluding the effects on cell walls)". [1] Alternatively, for samples which scatter light, absorbance may be defined as "the negative logarithm of one minus absorptance, as measured on a uniform sample". [2]
The absorbance of a material that has only one absorbing species also depends on the pathlength and the concentration of the species, according to the Beer–Lambert law =, where ε is the molar absorption coefficient of that material; c is the molar concentration of those species; ℓ is the path length.