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the flow cell and reaches the diode. The UV/VIS detector then produces a chromatogram as a two-dimensional (2D) output. This output plots time on the x-axis and response in absorbance units (AU) on the y-axis. The chromatogram is then analyzed by integrating the peaks curves to get their area, then getting their retention time (RT) from the peak maximum to identify them, and then perform quantitative analysis, by comparing their area to those of samples whose concentrations are known, i.e, standards.
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selected wavelength, reaching a photo-diode. The bench of the diode array detector, however, is configured so that the flow cell is positioned before the optical parts, so that the beam containing the entire spectrum is passing through it. The optical parts consist also with a monochromator and a slit, but with a fixed grating, which disperses the light onto a diode array imaging element.
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as a multi-wavelength UV-vis detector. This way they give additional information, which help understand more about the nature of the substances appearing in the chromatogram and allow their identification. Since the detector facilitates better peak identification it is the preferred detector for HPLC method development.
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that receives the light coming from the optical system and translates it into a signal proportional to light intensity. When the user selects a wavelength for the detector, the optical system rotates the grating or prism in the space, so that the desired wavelength passes through optical system, then
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In recent years, more advanced UV-VIS detectors have been increasingly used, based on diode arrays and entire spectrum collection at any given moment of data collection. They are called Diode Array detectors, and they collect entire UV spectra of every point the eluting peaks, while operating
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detectors, and the vast majority of them are variable wavelength detectors, which are in fact UV spectrophotometers on the flow. In this detector, it is decided in advance at which wavelength is needed for the detection, and its absorbance as function of time is collected in a graphic format called
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A schematic of the optical systems is shown in Figure 1. The variable UV-vis absorbance detector's optical bench is showing how the flow cell is positioned after the optical system, including the monochromator, which typically has a physical slit and a moving grating, so it is illuminated by a
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Figure 1: Simplified schemes of the
Variable UV-VIS detector compared to PhotoDiode Array detector. In the Variable UV-VIS the entire optical bench is located before the flow cell whereas in the diode array the flow rate is positioned before the main optical
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detector which measures the amount of ultraviolet or visible light absorbed by components of the mixture being eluted off the chromatography column. They are often used as detectors for
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L.C. Passos, Marieta; M.F.S. Saraiva, M. LĂşcia (2019).
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