Solid-liquid extraction is an operation with many applications: laboratory applications (sample preparation), industrial applications (extraction from vegetable. Liquid-solid extraction coupled with magnetic solid-phase extraction for determination of pyrethroid residues in vegetable samples by ultra fast. Liquid-Solid Extraction. In liquid-solid extraction, a solvent (hydrophilic or hydrophobic, acidic, neutral or basic) is added to a solid. Insoluble material can be.


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Solid/Liquid Extraction

The limits of detection for pyrethroid were between 0. Recoveries obtained by liquid solid extraction the four spiked vegetable samples were between Anion exchange[ edit ] Anion exchange sorbents are derivatized with positively charged functional groups that interact and retain negatively charged anions, such as acids.

Strong anion exchange sorbents contain quaternary ammonium groups that have a permanent positive charge in aqueous solutions, and weak anion exchange sorbents use amine groups liquid solid extraction are charged when the pH is below about 9.


Liquid solid extraction anion exchange sorbents are useful because any strongly acidic impurities in the sample will bind to the sorbent and usually will not be eluted with the analyte of interest; to recover a strong acid a weak anion exchange cartridge should be used.

To elute the analyte from either the strong or weak sorbent, the stationary phase is washed with a solvent that neutralizes the charge of either the analyte, the stationary phase, or both. Once the charge liquid solid extraction neutralized, the electrostatic interaction between the analyte and the stationary phase no longer exists and the analyte will elute from the cartridge.

Strong cation exchange sorbents contain aliphatic sulfonic acid groups that are always negatively charged in aqueous solution, and weak cation exchange sorbents contain aliphatic carboxylic acids, which are charged when the liquid solid extraction is above about 5.

Solid-Liquid Extraction

Once a soil sample has been collected from the site of interest, transfer it into the laboratory. Put the dish into an oven to dry for at least 12 h. Once dry, grind liquid solid extraction soil to a uniform powder with a mortar and pestle. Add 15 mL of hexane and loosely stopper the flask.

Solid Liquid Extraction Equipment for Industry | De Dietrich Process Systems

Place liquid solid extraction into an ultrasonic bath and sonicate for 60 min. Once sonication is complete, wet the paper with hexane and begin vacuum filtration. Slowly pour liquid solid extraction sample over the filter paper.

Rinse the residual solids from the flask with hexane and add it to the filter. The stripped soil remains on the filter, while the hexane and extracted organics collect in the flask.

If the hexane solution is cloudy, residual water is present. To dry the solution, add a small spatula of desiccant, such as calcium chloride.

Solid phase extraction - Wikipedia

Stir the solution until the desiccant is dissolved, and observe the solution. If the solution is still turbid or if the calcium chloride has liquid solid extraction, there is still water in the solution. Repeat the process until the solution is clear and the desiccant is free flowing.

Next, remove the calcium chloride by liquid solid extraction filtration. If the concentration of the compound of interest is below the limit of quantification, it must be concentrated.

Transfer the filtered extract to a clean, dry 3-necked round-bottom flask.

Solid-Liquid Extraction | Protocol

Stopper the center neck, and place a rubber septum over one of the other necks. The third is left open.

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Pierce the septum and attach tubing to a nitrogen line. Begin flowing nitrogen through the flask. The gas should be flowing in the headspace above the solution, and not bubbling through it. The liquid solid extraction gas evaporates the excess solvent.