Name: ion exchange resins and charged molecules
Uploaded: 2024-04-04T10:51:25.000Z
Duration: 1 min 17 s
Channel: JoVE

Wymiana jonowa oddziela naładowane cząsteczki od roztworu poprzez odwracalną wymianę ich na ruchome lub "aktywne" jony związane z przeciwnie naładowaną fazą stacjonarną.
Faza stacjonarna jest zwykle porowatym, ale nierozpuszczalnym ciałem stałym, takim jak usieciowane polimery organiczne o dużej masie cząsteczkowej, które mają dużą liczbę monomerów zawierających jonowe grupy funkcyjne.
Polimery anionowe z aktywnymi kationami są wymieniaczami kationowymi, podczas gdy polimery kationowe z aktywnymi anionami są wymieniaczami anionowymi.
Wymieniacze kationowe i anionowe są dalej klasyfikowane jako słabe i silne w oparciu o ich grupy funkcyjne.
Ruchome jony przyłączone do wymieniaczy jonowych migrują do roztworu i są zastępowane podobnie naładowanymi jonami z roztworu, aż do osiągnięcia równowagi.
Zastosowanie prawa działania masy do równowagi jonowymiennej wyraża współczynnik selektywności dla reakcji.
Wyczerpane wymieniacze kationowe i anionowe są regenerowane poprzez przemywanie ich nadmiarem odpowiednio roztworów kwaśnych lub zasadowych.

wymiana jonowa

Ion Exchange

Chromatografia jonowymienna oddziela naładowane cząsteczki od roztworu poprzez odwracalną wymianę ich na ruchome, czyli „aktywne” jony związane z przeciwnie naładowaną fazą stacjonarną. Metodę tę można zastosować do oddzielania jonów, zmiękczania i dejonizacji wody oraz oczyszczania roztworów. Polimery tworzące kolumnę jonowymienną są polimerami o dużej masie cząsteczkowej i chemicznie stabilnymi, usieciowanymi tak, aby były porowate i zasadniczo nierozpuszczalne. Są one również funkcjonalizowane grupami kwasowymi lub zasadowymi. Kolumny lub żywica funkcjonalizowane grupami kwasowymi nazywane są wymieniaczami kationowymi i zawierają ujemnie naładowane polimery z dodatnimi przeciwjonami. Umożliwiają one wymianę kationów z fazy ruchomej. Kolumny lub żywica funkcjonalizowane grupami zasadowymi nazywane są wymieniaczami anionowymi, które zawierają dodatnio naładowane polimery z ujemnymi przeciwjonami i wymieniają aniony z roztworu.

Podczas wymiany jonowej przeciwjony związane z polimerami w fazie stałej dostają się do roztworu, natomiast jony z roztworu oddziałują zamiast tego z polimerem. Należy zauważyć, że zdolność do wymiany jonów wzrasta wraz ze wzrostem stopnia usieciowania i wzrostem liczby grup jonowymiennych w polimerze. Wymiana ta jest odwracalna i trwa do momentu ustalenia równowagi.

Kwaśne wymieniacze kationowe można funkcjonalizować albo mocnymi kwasami, takimi jak kwas sulfonowy (-SO3H), występującymi w kwasie polistyrenosulfonowym, lub słabymi kwasami, takimi jak kwas karboksylowy (-COOH), występującymi w kwasie poli(metylometyloakrylowym). Podobnie wymieniacze anionowe są klasyfikowane jako mocne i słabe. Silne wymieniacze anionowe często zawierają czwartorzędowe grupy amoniowe (−CH2N(CH3)3+), takie jak te w czwartorzędowym chlorku amonu polistyrenu, a słabe wymieniacze anionowe są często funkcjonalizowane podstawionymi aminami (−NH3+), takimi jak te w wodorotlenku trzeciorzędowej aminy polistyrenu .

Wymiana jonowa

Wymiana jonowa oddziela naładowane cząsteczki od roztworu poprzez odwracalną ich wymianę na ruchome lub "aktywne" jony związane z ...

Education

JoVE Core

Analytical Chemistry

Chemia analityczna

Unit 1

Jednostka 1

Introduction to Separation Methods

Wstęp do metod rozdziału

KEY TERMS AND CONCEPTS

KLUCZOWE POJĘCIA I KONCEPCJE

ion exchange resins and charged molecules

Ion exchange chromatography separates charged molecules from a solution by swapping them with mobile, or active, ions on a stationary phase. It is used to separate ions, soften and deionize water, and purify solutions. The method depends on a solid column made of high-molecular-weight, chemically stable polymers that are crosslinked to make them porous and essentially insoluble.

These polymers are functionalized with either acidic or basic groups. When acidic groups are present, the resin is a cation exchanger. It has a negatively charged polymer with positive counterions, so it can exchange cations from the mobile phase.

When basic groups are present, the resin is an anion exchanger. It has a positively charged polymer with negative counterions, so it can exchange anions from the solution. During ion exchange, the counterions on the solid polymer move into the solution, and ions from the solution take their place.

The exchange is reversible and continues until equilibrium is reached. The ability to exchange ions increases when the polymer has more crosslinking and more ion-exchange groups. Cation exchangers can be strong or weak. Strong cation exchangers often use sulfonic acid groups, such as in polystyrene sulfonic acid, while weak cation exchangers often use carboxylic acid groups, such as in poly(methyl methylacrylic) acid.

Anion exchangers are also classified as strong or weak. Strong anion exchangers often contain quaternary ammonium groups, such as in polystyrene quaternary ammonium chloride. Weak anion exchangers are often functionalized with substituted amines, such as in polystyrene tertiary amine hydroxide.

Ion Exchange Resins and Charged Molecules

ion-exchange-resins-and-charged-molecules

states of matter and phase changes

Heating and Cooling During Phase Changes

Heating and cooling can change a substance from one state of matter to another. These phase changes depend on internal energy, which is the total kinetic energy of particles and the potential energy from their interactions. In the condensed phases, stronger intermolecular forces and the pressure on the substance affect that internal energy. The internal energy is highest in the gaseous state, lowest in the solid state, and in between for the liquid state. Phase transitions happen when...

distillation: vapor&ndash;liquid equilibria

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

Filtration separates a solid from a liquid by passing a suspension through a porous medium. The solid stays on the filter, and the liquid, called the filtrate, passes through. This makes filtration a physical separation process, not a chemical change. The filtering medium is chosen for the purpose of the separation, the amount of material, and the nature of the precipitate. A good filter medium should be inert, mechanically strong, nonabsorbent toward dissolved materials, and able to let...

centrifugation

Centrifugation for Separating Particles

Centrifugation separates particles in a liquid by using differences in size and density. The sample is placed in centrifugation tubes and spun at high angular velocity. This creates centrifugal force, which makes the different components move at different rates. After spinning, the supernatant, or liquid above the settled material, is decanted. In some cases, the pellet is kept for further purification. In other cases, the supernatant is kept and may be spun again for additional processing. <br...

sublimation

Sublimation in Separation and Purification

Sublimation is the direct change of a solid into a gas. It skips the liquid state. A common example is solid carbon dioxide, or dry ice, which turns into gaseous carbon dioxide at standard pressure and room temperature. The phase diagram shows when sublimation can happen. This process occurs at the solid-gas boundary. It is not seen above the triple point of a substance. The reverse process is deposition, which is when a gas changes directly into a solid. Sublimation and deposition can help...

recrystallization: solid&ndash;solution equilibria

recrystallization-solidsolution-equilibria

Recrystallization for Purifying Solid Compounds

Recrystallization is a way to purify solid compounds by using differences in solubility. It does not involve a chemical reaction. Instead, it relies on physical properties of the desired compound and the impurities. The process is based on solid-solution equilibrium, also called solubility equilibrium. In this equilibrium, a component is split between the solid phase and the solution phase. At equilibrium, the chemical potential of that component is the same in both phases. To begin...

crystal growth: principles of crystallization

crystal-growth-principles-of-crystallization

Crystal Formation Through Supersaturation

Crystal formation through supersaturation begins when a solution contains more dissolved solute than it can normally hold. In crystallization, atoms or molecules line up into a rigid crystal lattice so the system can lower its energy. To start the process, the solute concentration and the solution temperature must be adjusted so the supersaturation ratio, S, is greater than one. Supersaturation can be increased in two main ways. One method is to concentrate the solution by evaporating the...

precipitation and co-precipitation

Selective Ion Separation by Precipitation

Selective ion separation by precipitation is used to isolate ions from a solution. In qualitative inorganic analysis, ions that form sparingly soluble precipitates with the same reagent can be separated by using differences in their solubility products. A solubility product is the limit at which an ionic solid begins to form from dissolved ions. One example is the separation of Cu(II) and Fe(II) ions as insoluble sulfides. Copper(II) sulfide is first precipitated by adding acidic H2S. The acid...

coagulation

Wastewater Cleanup by Coagulation

Coagulation helps remove colloidal particles from wastewater. Colloids are tiny solid particles suspended in a liquid. They are usually negatively charged, so they attract a compact first layer of positive ions. More counterions gather around them and form an electrical double layer. This charge barrier keeps the particles apart and stabilizes the colloid. These suspended solids can be a problem because they may contain toxins that are hard to remove. Coagulation is used to make the particles...

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

extraction-partition-and-distribution-coefficients

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

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

Chelate extraction is a way to separate metal ions by using an organic ligand, or chelating agent, to form an uncharged metal complex. The chelating agent needs hydrophobic groups, and it must act as a weak acid so it can lose a proton and bind to the metal. Most organic ligands used for this method are not stable in water or are insoluble in the aqueous phase. For that reason, the chelating agent is first placed in the organic phase. It then moves into the aqueous phase, where the...

chromatography: introduction

Chromatography: Separation by Polarity

Chromatography separates compounds by how they divide between a stationary phase and a mobile phase. The stationary phase is the material that holds the compounds for a time. The mobile phase is the solvent that carries the solutes to be analyzed. In column chromatography, a mixture flows through the stationary phase. The compounds separate based on their structure and polarity. Solutes that interact weakly with the stationary phase move faster through the column and exit first. Solutes that...

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

Volatilization gravimetry is a way to measure mass loss in a sample by driving off a volatile substance. It helps estimate how much volatile material is present. In this method, a known amount of sample is heated to a high temperature in a crucible or another suitable vessel. As the sample heats, the volatile substance evaporates. The vapor is then completely removed from the crucible, either by continued heating or by bubbling an inert gas through the vessel. The non-volatile part stays...

ion exchange

Ion exchange chromatography separates charged molecules from a solution by swapping them with mobile, or active, ions on a stationary phase. It is used to separate ions, soften and deionize water, and purify solutions. The method depends on a solid column made of high-molecular-weight, chemically stable polymers that are crosslinked to make them porous and essentially insoluble. These polymers are functionalized with either acidic or basic groups. When acidic groups are present, the resin is a...

key terms and concepts

Learn how ion exchange chromatography uses cation and anion exchangers to separate charged molecules, purify solutions, and soften water.

Ion Exchange Resins and Charged Molecules | JoVE K12

analytical chemistry

JoVE Core Analytical Chemistry simplifies complex chemical principles by breaking them down into clear, engaging animations, making topics from SI Units to NMR spectroscopy more accessible and straightforward. Additionally, the scientist-in-action videos highlight the application of these concepts in real-world research conducted in laboratories globally.

Ion Exchange Resins and Charged Molecules

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