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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 chemistry, biochemistry, and other fields, to identify and quantify compounds in a variety of samples.
There are some common types of spectrophotometers include: UV-vis spectrophotometer: Measures light absorption in UV and visible ranges (200-800 nm). Used for quantification of many inorganic and organic compounds. 1. Infrared spectrophotometer: Measures infrared light absorption, allowing identification of chemical bonds and functional groups. 2.
Ultraviolet–visible spectroscopy (UV–vis) can distinguish between enantiomers by showing a distinct Cotton effect for each isomer. UV–vis spectroscopy sees only chromophores, so other molecules must be prepared for analysis by chemical addition of a chromophore such as anthracene.
For UV-Vis spectroelectrochemistry, spectrometer must be specific for UV-Vis spectral region. Potentiostat / Galvanostat : electronic device that allows controlling the working electrode potential regarding to the reference electrode or controlling the current that passes respect to the auxiliary electrode .
The DU was developed at National Technical Laboratories (later Beckman Instruments) under the direction of Arnold Orville Beckman, an American chemist and inventor. [13] [14] Beginning in 1940, National Technical Laboratories developed three in-house prototype models (A, B, C) and one limited distribution model (D) before moving to full commercial production with the DU in 1941.
Diffuse reflectance spectroscopy, or diffuse reflection spectroscopy, is a subset of absorption spectroscopy.It is sometimes called remission spectroscopy.Remission is the reflection or back-scattering of light by a material, while transmission is the passage of light through a material.
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 dispersive method is more common in UV-Vis spectroscopy, but is less practical in the infrared than the FTIR method. One reason that FTIR is favored is called " Fellgett's advantage " or the "multiplex advantage": The information at all frequencies is collected simultaneously, improving both speed and signal-to-noise ratio .