Name: ph control in liquid extraction
Uploaded: 2024-04-04T10:51:24.000Z
Duration: 53 s
Channel: JoVE

K12 Standards

Tennessee Academic Standards

High School

Chemistry

Matter and Its Interactions

CHEM1.PS1.7

Extraction: Effects of pH

Consider a weak base,&#160; B, with a partition coefficient, K, between the organic and aqueous phases.&#160;&#160;
While organic bases are usually more soluble in the organic phase, changing the pH can convert them to their water-soluble salt form.
Here, the conjugate acid, BH+, has the acid dissociation constant Ka.&#160;
If BH+ is soluble only in the aqueous phase, then the distribution coefficient, D,&#160; can be calculated from the total concentration of B.
Substituting for K and Ka and rearranging gives the fraction of neutral base in the aqueous phase.
The pH-dependent distribution ratio implies that a base can be extracted into the aqueous phase as its conjugate acid within a suitable pH range.

extractie: effect van ph

Beschouw een neutrale vorm van een amine, B, met een verdelingscoëfficiënt K, in een vloeibaar mengsel dat organische en waterige fasen bevat. De pH van de waterfase beïnvloedt de lading van zure en basische opgeloste stoffen, en de geladen vorm is gewoonlijk beter oplosbaar in de waterfase. Veronderstel dat de geconjugeerde zuurvorm van het amine alleen oplosbaar is in de waterfase, terwijl de basevorm in beide fasen oplosbaar is. Vervolgens kan de verdelingscoëfficiënt D worden gegeven als de verhouding van de amineconcentratie in de organische fase tot de som van de concentraties van het amine en het geconjugeerde zuur ervan in de waterfase. In deze vergelijking kunnen de termen voor de verdelingscoëfficiënt en de zuurdissociatieconstante, Ka, worden vervangen door de concentraties, en kan de fractie neutraal amine in de waterfase worden bepaald door de vergelijking op te lossen. Met ladderdiagrammen en een grafiek van log D versus pH kan worden geconcludeerd dat een neutrale base kan worden geëxtraheerd in de waterige fase bij een pH die laag genoeg is om deze om te zetten in het geladen conjugaat zuur. Op soortgelijke wijze kan een geladen zuur in de organische fase worden geëxtraheerd bij een pH die hoog genoeg is om het in zijn neutrale geconjugeerde base om te zetten.

Extractie: effect van pH

Consider a weak base,&#160; B, with a partition coefficient, K, between the organic and aqueous phases.&#160;&#160;
While organic bases are usually more ...

Education

JoVE Core

Analytical Chemistry

Analytische chemie

Unit 1

Introduction to Separation Methods

Inleiding tot scheidingsmethoden

KEY TERMS AND CONCEPTS

BELANGRIJKE TERMEN EN CONCEPTEN

ph control in liquid extraction

pH control in liquid extraction changes how amines and acids move between organic and aqueous phases. The pH of the aqueous phase affects the charge on acidic and basic solutes. The charged form is usually more soluble in the aqueous phase.

For a weak base such as an amine, the neutral form is called B. Its partition coefficient, K, describes how the neutral molecule distributes between the two liquids. If the conjugate acid of the amine is soluble only in the aqueous phase, while the base form is soluble in both phases, the distribution coefficient, D, can be written from the amine level in the organic phase and the total of the amine plus its conjugate acid in the aqueous phase.

The equation for D can be rewritten by using concentrations, the partition coefficient, and the acid dissociation constant, Ka. This makes it possible to solve for the fraction of neutral amine in the aqueous phase. Ladder diagrams and a plot of log D versus pH help show the same pattern.

These pH trends show when extraction will favor one layer over the other. A neutral base can be extracted into the aqueous phase if the pH is low enough to convert it into its charged conjugate acid. A charged acid can be extracted into the organic phase if the pH is high enough to convert it into its neutral conjugate base.

pH Control in Liquid Extraction

states of matter and phase changes

Heating and Cooling During Phase Changes

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Distillation and Boiling Point Changes

Distillation separates a miscible liquid mixture by using differences in boiling points. It works best when the two liquids have a significant boiling point gap, usually at least 20°C. In this process, the mixture is heated until the more volatile component reaches its bubble point and begins to vaporize. The vapor then rises into a condenser. A condenser is a glass tube with separate inner and outer sections. Cold water flows through the outer section and cools the vapor in the inner section,...

filtration

Filtration Setup and Filtrate Collection

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centrifugation

Centrifugation for Separating Particles

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sublimation

Sublimation in Separation and Purification

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recrystallization: solid&ndash;solution equilibria

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Recrystallization for Purifying Solid Compounds

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crystal growth: principles of crystallization

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Crystal Formation Through Supersaturation

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precipitation and co-precipitation

Selective Ion Separation by Precipitation

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coagulation

Wastewater Cleanup by Coagulation

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electrodeposition

Electrodeposition for Metal Ion Separation

Electrodeposition separates metal ions from a solution by using an electric current and an electrolytic cell. The cell has an anode and a cathode. When current flows, oxidation happens at the anode. At the cathode, metal ions gain electrons, undergo reduction, and deposit on the large metal surface. This method works well when metals have very different reduction potentials. Copper and nickel in the same solution can be separated this way. First, the solution is made acidic. Then current is...

extraction: partition and distribution coefficients

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Solvent Partitioning in Chemical Extraction

Solvent partitioning in chemical extraction describes how a solute spreads between two immiscible solvents. Immiscible solvents do not mix, such as an aqueous phase and an organic phase. The distribution law, also called Nernst's distribution law or the partition law, explains how that solute is shared at a constant temperature and equilibrium. At equilibrium, the ratio of solute concentrations in the two solvents stays constant. For extraction from water into an organic solvent, this...

extraction: effects of ph

pH control in liquid extraction changes how amines and acids move between organic and aqueous phases. The pH of the aqueous phase affects the charge on acidic and basic solutes. The charged form is usually more soluble in the aqueous phase. For a weak base such as an amine, the neutral form is called B. Its partition coefficient, K, describes how the neutral molecule distributes between the two liquids. If the conjugate acid of the amine is soluble only in the aqueous phase, while the base...

extraction: advanced methods

Chelate Extraction for Metal Ion Separation

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Chromatography: Separation by Polarity

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dialysis

Dialysis Separation by Diffusion

Dialysis separates small molecules from larger ones by diffusion through a semipermeable membrane. It is a purification method used to remove unwanted ions or small organic molecules from a sample while keeping larger analytes in place. The membrane is usually made of cellulose acetate or cellulose nitrate. Its pores are typically about 1 to 5 nm wide. Molecules such as chloride, sodium, and glucose can pass through these pores. Larger molecules, including proteins, hormones, and enzymes, are...

volatilization

Mass Loss in Gravimetric Analysis

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ion exchange

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key terms and concepts

See how pH changes the charge and solubility of acids and amines during liquid extraction, using partition coefficient, Ka, and log D behavior.

pH Control in Liquid Extraction | JoVE K12

analytical chemistry

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CHEM1.PS1.1

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Demonstrate that atoms, and therefore mass, are conserved during a chemical reaction by balancing chemical reactions. EXPLANATION: Standard 7.PS1.4 explores the idea that chemical reactions are rearrangements of atoms, and students undertake the process of balancing chemical reactions with that standard in seventh grade. The introduction of molar masses in high school makes an explicit connection between the number of atoms, as previously investigated, and the actual masses of the atoms, permitting the collection of more concrete evidence for the conservation of mass in chemical reactions.

CHEM1.PS1.2

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Perform stoichiometric calculations involving the following relationships: mole- mole; mass-mass; mole-mass; mole- particle; and mass- particle. Show a qualitative understanding of the phenomenon of percent yield, limiting, and excess reagents in a chemical reaction through pictorial and conceptual examples. (states of matter liquid and solid; excluding volume of gasses). EXPLANATION: This standard builds on the idea that balancing chemical reactions provides evidence for conservation of mass and that the behavior of atoms follows predictable patterns. Students now have the opportunity to utilize this understanding as they perform and evaluate chemical reactions. (The concepts of limiting reagent and percent yield are presented; however, students are not expected to determine these values algebraically. Use of molar volume in stoichiometric processes is beyond the scope of this standard.)

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Use the reactants in a chemical reaction to predict the products and identify reaction classes (synthesis, decomposition, combustion, single replacement, double replacement). EXPLANATION: Chemical reactions are rearrangements of atoms that follow predicable patterns. There are patterns both at the macroscopic level in the behavior of some of the reaction classes, as well as patterns in the rearrangements of the atoms underlying the reaction. Students should be able to predict the products of the reactions, which also requires the ability to recognize the general patterns for each type of reaction.

CHEM1.PS1.4

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Conduct investigations to explore and characterize the behavior of gasses (pressure, volume, and temperature), develop models to represent this behavior, and construct arguments to explain this behavior. Evaluate the relationship (qualitative and quantitatively) at STP between pressure and volume (Boyle's Law), temperature and volume (Charles' Law), temperature and pressure (Gay-Lussac Law) and moles and volume (Avogadro's Law), and evaluate and explain these relationships with respect to kinetic molecular theory. Be able to understand, establish, and predict the relationships between volume, temperature, and pressure using combined gas law both qualitatively and quantitatively. EXPLANATION: When exploring the behavior of gasses, it is important to consider experimental design. Experiments used to show the relationships between these sets of variables should include one independent and one dependent variable. Other variables should be held constant. Pressure should serve as the dependent variable because it cannot be manipulated directly. Avogadro's Law can be used to relate the amount of gas in two different containers in lieu of knowing actual number of gas particles in an individual container. Individual demonstrations can be performed to explore each of the different gas laws.

CHEM1.PS1.5

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CHEM1.PS1.6

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Analyze solutions to identify solutes and solvents, quantitatively analyze concentrations (molarity, percent composition, and ppm), and perform separation methods such as evaporation, distillation, and/or chromatography and show conceptual understanding of distillation. Construct argument to justify the use of certain separation methods under different conditions. EXPLANATION: In seventh grade, students developed an understanding that chemical and physical properties of a sample of matter could be used to identify a substance. Building on this understanding, students now explore the use of these physical and chemical properties to separate mixtures. Analysis of the substances is performed to aid in further discussion and facilitate further quantitative analysis.

pH Control in Liquid Extraction

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