How does solid-supported liquid-liquid extraction differ from solid-phase extraction?

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The difference between solid supported liquid-liquid extraction and solid –phase extraction is explained.

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01

Defining liquid-liquid extraction and solid-phase extraction.

  • The extraction technique can be used to purify compounds or separate compound mixtures, such as isolating a product from a reaction mixture (known as an extractive work-up). It can also be used to isolate natural products, such as caffeine from tea leaves.
  • Solid-Phase Extraction (SPE) is a sample preparation method that is used in a variety of fields due to its numerous advantages over other traditional methods. SPE was developed as an alternative to liquid/liquid extraction because it eliminated several disadvantages, including the use of a large amount of solvent, extended operation time/procedure steps, potential sources of error, and high cost.
02

Determining the difference between liquid-liquid extraction and solid-phase extraction.

(1) Solid-supported liquid-liquid extraction:

  • Aqueous phase remains suspended in a microporous medium where organic solvent is passed through in order to extract analytes
  • Liquid extraction, also known as partitioning, is a separation process that involves the transfer of a solute from one solvent to another, with the two solvents being immiscible or partially miscible.

(2) Solid-phase extraction:

  • Aqueous sample passes through small column of the stationary phase which retains analytes
  • Analytes and impurities are eluted by washing it many times with small volumes of solvent with an increase in the solvent strength
  • Furthermore, SPE can be applied to samples in conjunction with other analytical methods and sample preparation techniques.
  • Because of its versatility, the SPE technique is a useful tool for a variety of purposes. The main approaches in this method's practises are isolation, concentration, purification, and cleanup.

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Most popular questions from this chapter

The following wet-ashing procedure was used to measure arsenic in organic soil samples by atomic absorption spectroscopy: A 0.1- to \({\bf{0}}.{\bf{5}} - \)g sample was heated in a \({\bf{150}} - {\bf{mL}}\) Teflon bomb in a microwave oven for \(2.5\;{\rm{min}}\) with \(3.5\;{\rm{mL}}\)of\(70\% \,\,\,{\rm{HN}}{{\rm{O}}_3}\). After the sample cooled, a mixture containing \(3.5\;{\rm{mL}}\)of \(70\% \,\,\,{\rm{HN}}{{\rm{O}}_3},1.5\;{\rm{mL}}\) of\(70\% \,\,{\rm{HCl}}{{\rm{O}}_4}\), and \(1.0\;{\rm{mL}}\) of \({{\rm{H}}_2}{\rm{S}}{{\rm{O}}_4}\)was added and the sample was reheated for three \({\bf{2}}.{\bf{5}} - {\bf{min}}\) intervals with 2 -min unheated periods in between. The final solution was diluted with \(0.2{\rm{M}}\,\,\,{\rm{HCl}}\)for analysis. Why was \({\rm{HCl}}{{\rm{O}}_4}\) not introduced until the second heating?

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