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Related Concept Videos

UV–Vis Spectrometers01:14

UV–Vis Spectrometers

The absorbance of UV and visible (UV–visible) radiations is measured using a UV–visible spectrophotometer. Deuterium lamps, which emit UV radiation, and tungsten lamps, which produce radiation in the visible region, are used as light sources in UV–visible spectrophotometers. A monochromator or prism is used for diffraction grating, i.e., to split the incoming radiation into different wavelengths. A system of slits is used to focus the desired wavelength on the sample cell. Samples for...
Ultraviolet and Visible (UV–Vis) Spectroscopy: Overview01:02

Ultraviolet and Visible (UV–Vis) Spectroscopy: Overview

Ultraviolet–visible (UV–visible or UV–Vis) spectroscopy is an analytical technique that investigates the interaction between matter and UV–Vis light within the electromagnetic spectrum. This method is widely used for its versatility, simplicity, and relatively quick data acquisition, making it valuable for both qualitative and quantitative analysis. When UV–Vis radiation passes through a material,  molecules absorb light depending on the energy required for electronic transitions. As a result...
UV–Vis Spectroscopy: Beer–Lambert Law01:09

UV–Vis Spectroscopy: Beer–Lambert Law

The Beer-Lambert law describes the relationship between absorbance and concentration, which combines the principles established by scientists Johann Heinrich Lambert and August Beer. Lambert's law states that when light passes through a medium, the loss in intensity is directly proportional to the original intensity and the path length of the light. Beer's law proposed that the transmittance of a solution remains constant if the product of concentration and path length is constant. The modern...
Spectrophotometry: Introduction01:16

Spectrophotometry: Introduction

Spectrophotometry is the quantitative measurement of the absorption, reflection, diffraction, or transmission of electromagnetic radiation through a material as a function of the intensity and wavelength of the radiation. A spectrophotometer is a device used to measure the change in the radiation intensity caused by its interaction with the material.
The essential components of a spectrophotometer include a source of electromagnetic radiation, a slot for placing a material to be analyzed, and a...
IR Spectrometers01:25

IR Spectrometers

There are two main infrared (IR) spectrophotometers: dispersive IR spectrometers and Fourier transform infrared (FTIR) spectrometers. In a dispersive IR spectrometer, a beam of infrared radiation produced by a hot wire is divided into two parallel equal-intensity beams using mirrors. One beam passes through the sample, while another is a reference beam. The beams then move through the monochromator, which separates the radiations into a continuous spectrum of different frequencies. The...
UV–Vis Spectrum01:30

UV–Vis Spectrum

When light passes through a substance, a portion of the light is absorbed while the remaining light is reflected or transmitted. If the molecule absorbs light between the wavelengths of 180–400 nm range, the UV spectrum is obtained, and if it absorbs light in the 400–780 nm wavelength range, the visible spectrum is obtained.     
The UV–Vis spectrum of a molecule is the plot of its absorbance versus wavelength. The plot is drawn by taking molar absorptivity (ε) or log ε on the y-axis (ordinate)...

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UV-Vis Spectroscopic Characterization of Nanomaterials in Aqueous Media
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UV-Vis Spectroscopic Characterization of Nanomaterials in Aqueous Media

Published on: October 25, 2021

Ultraviolet refractometry using field-based light scattering spectroscopy.

Dan Fu1, Wonshik Choi, Yongjin Sung

  • 1G R Harrison Spectroscopy Laboratory, Massachusetts Institute of Technology. Cambridge, Massachusetts 02139, USA.

Optics Express
|April 8, 2010
PubMed
Summary
This summary is machine-generated.

A new method uses light scattering spectroscopy to measure the refractive index of biomolecules like proteins and DNA in the deep UV range. This technique offers high accuracy for quantifying biological samples.

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Area of Science:

  • Biophysics
  • Spectroscopy
  • Materials Science

Background:

  • Accurate refractive index measurement in the deep UV range is crucial for quantifying biomolecules like proteins and DNA.
  • Existing methods face challenges in this specific spectral region, limiting applications in biological analysis.

Purpose of the Study:

  • To introduce a novel field-based light scattering spectroscopy method for precise refractive index measurements.
  • To demonstrate the method's applicability across various wavelengths and sample types, including solutions and microspheres.

Main Methods:

  • Utilized quantitative phase microscopy to measure angular scattering distributions of single microspheres (260-315 nm).
  • Applied Mie scattering theory with least-squares fitting to determine refractive indices.
  • Measured refractive index dispersion for SiO(2) spheres and bovine serum albumin (BSA) solutions.

Main Results:

  • Achieved typical accuracy of <=0.003 and precision of <=0.002 for refractive index measurements.
  • Successfully extracted specific refractive index increments for BSA solutions.
  • Demonstrated the method's effectiveness in the challenging deep UV spectral range.

Conclusions:

  • The developed light scattering spectroscopy method provides accurate and precise refractive index measurements in the deep UV.
  • This technique is versatile, applicable to diverse samples and wavelengths, advancing biomolecular quantification.
  • The method enables detailed characterization of materials and solutions, including specific refractive index increments.