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Related Concept Videos

Silica Gel Column Chromatography: Overview01:10

Silica Gel Column Chromatography: Overview

Silica gel column chromatography is a technique for separating compounds using a column packed with silica gel as the stationary phase. This method relies on differences in the polarity of compounds. Based on their polarities, compounds move between the stationary phase (silica gel) and the mobile phase (the solvent), forming discrete bands in the column.
Polar components tend to bind strongly to the silica gel, causing them to move slowly through the column. In contrast, nonpolar compounds...
Ion Exchange01:17

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Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or basic...
Principles Of Column Chromatography01:13

Principles Of Column Chromatography

The chromatography technique was first invented in 1901 by Michael S. Tswett, a Russian botanist, to separate plant pigments using organic solvents. Further, in 1941, Archer John Porter Martin and R. L. M. Synge modified the technique by packing silica gel into a column. A mixture of amino acids was then separated on the packed column using chloroform and water mixture as the mobile phase. This was the first report on column chromatography. At present, column chromatography is a widely used...
Size-Exclusion Chromatography01:08

Size-Exclusion Chromatography

In size-exclusion chromatography (SEC), also known as molecular-exclusion or gel-permeation chromatography, molecules are separated based on their sizes. This technique is important for separating large molecules such as polymers and biomolecules. The two classes of micron-sized stationary phases encountered in SEC are silica particles and cross-linked polymer resin beads. Both materials are porous, but their pore sizes vary significantly.
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Gas Chromatography: Types of Columns and Stationary Phases01:17

Gas Chromatography: Types of Columns and Stationary Phases

Gas chromatography (GC) relies on stationary phases to separate and analyze components in a sample. There are two main types of stationary phases: liquid and solid. Liquid stationary phases are non-volatile, thermally stable, and chemically inert liquids coated onto the column. Solid stationary phases are particles of adsorbent material, such as silica gel or molecular sieves.
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Qualitative Characterization of the Aqueous Fraction from Hydrothermal Liquefaction of Algae Using 2D Gas Chromatography with Time-of-flight Mass Spectrometry
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Separation of fructooligosaccharides using zeolite fixed bed columns.

Raquel Cristine Kuhn1, Francisco Maugeri Filho

  • 1Laboratory of Bioprocess Engineering, Food Engineering Department, P.O. Box 6121, University of Campinas, 13083-862 Campinas, SP, Brazil. raquelk@fea.unicamp.br

Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences
|July 10, 2010
PubMed
Summary

Y zeolites enhance fructooligosaccharide (FOS) separation. Optimized conditions using Ba2+-exchange Y zeolites improve chromatographic separation of FOS mixtures, aiding in analysis.

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Hierarchical and Programmable One-Pot Oligosaccharide Synthesis
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Qualitative Characterization of the Aqueous Fraction from Hydrothermal Liquefaction of Algae Using 2D Gas Chromatography with Time-of-flight Mass Spectrometry
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09:56

Hierarchical and Programmable One-Pot Oligosaccharide Synthesis

Published on: September 6, 2019

Area of Science:

  • Carbohydrate Chemistry
  • Separation Science
  • Analytical Chemistry

Background:

  • Y zeolites show potential for improving chromatographic separation of mono-, di-, and oligosaccharides.
  • Fructooligosaccharides (FOS) are important carbohydrates with various applications.
  • Enzymatic production of FOS yields mixtures including kestose (GF2), nystose (GF3), and frutofuranosyl nystose (GF4).

Purpose of the Study:

  • To investigate the chromatographic separation of fructooligosaccharides (FOS) using a column packed with zeolite.
  • To optimize separation conditions for FOS mixtures using Ba2+-exchange Y zeolites.
  • To determine the effects of temperature, injection volume, superficial velocity, and eluent composition on separation efficiency.

Main Methods:

  • Fructooligosaccharides were produced enzymatically from Rhodotorula sp.
  • Separation and analysis were performed using ion exchange chromatography with pulsed amperometric detection (HPAEC-PAD).
  • A fractional factorial design was employed to investigate the effects of operational parameters on separation efficiency using Ba2+-exchange Y zeolites.

Main Results:

  • Optimal separation conditions were identified as 60% ethanol eluent, 50°C temperature, 0.1 cm/min superficial velocity, and 2.55% injection volume, using two columns in series.
  • High separation efficiencies were achieved for various sugar pairs, including oligosaccharide-fructose (1.00) and fructose-sucrose (1.23).
  • The study demonstrated the effectiveness of Ba2+-exchange Y zeolites for FOS separation.

Conclusions:

  • Ba2+-exchange Y zeolites provide an effective method for the chromatographic separation of fructooligosaccharides.
  • Optimized parameters significantly enhance the separation efficiency of FOS mixtures.
  • This method holds promise for the analysis and purification of oligosaccharides.