Search results
Results from the WOW.Com Content Network
Two other issues that must be considered in setting up an absorption spectroscopy experiment include the optics used to direct the radiation and the means of holding or containing the sample material (called a cuvette or cell). For most UV, visible, and NIR measurements the use of precision quartz cuvettes are necessary.
Single-beam scanning spectrophotometer. There are two major classes of devices: single-beam and double-beam. A double-beam spectrophotometer [13] compares the light intensity between two light paths, one path containing a reference sample and the other the test sample. A single-beam spectrophotometer measures the relative light intensity of the ...
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]
Parameters of interest, besides the wavelength of measurement, are absorbance (A) or transmittance (%T) or reflectance (%R), and its change with time. [4] [5] A UV-Vis spectrophotometer is an analytical instrument that measures the amount of ultraviolet (UV) and visible light that is absorbed by a sample. It is a widely used technique in ...
The absorbance measured by the Spectronic 20 is the sum of the absorbance of each of the constituents of the solution. Therefore, the Spectronic 20 can be used to analyze more complex solutions. For example, if a sample solution has two light-absorbing compounds in it, then the user performs measurements at two different wavelengths and ...
Saturated absorption spectroscopy measures the transition frequency of an atom or molecule between its ground state and an excited state.In saturated absorption spectroscopy, two counter-propagating, overlapped laser beams are sent through a sample of atomic gas.
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.
This shows that the absorbance values on the plot are offset by an equal amount and the slope of the two plots are equal. Thus, the concentration calculated from the two plots is equal. Other scalar components that contribute to the absorbance of a given sample like contaminants on the cuvette or a different cuvette material also are averaged ...