Name: activity coefficient in ionic solutions
Uploaded: 2024-04-04T10:51:15.000Z
Duration: 1 min 24 s
Channel: JoVE

활동은 효과적인 집중의 척도입니다. 그것은 단위가 없으며 종의 몰 농도와 그 활성 계수의 곱으로 표현 될 수 있습니다.
이상적인 거동으로부터의 편차를 측정하는 무차원 양인 활성 계수는 이온 강도에 따라 다릅니다. 이상적인 솔루션에서 활동은 집중과 같습니다.
이온 강도가 매우 낮은 용액에서 이온의 활성 계수는 통일성에 가깝고 거동은 본질적으로 이상적입니다.
이온 강도가 증가함에 따라 활성 계수는 단위보다 작아지며, 이는 활성이 농도보다 낮은 이상성에서 벗어남을 나타냅니다.
그러나 이온 강도가 매우 높은 용액에서는 활성 계수가 단일성을 초과할 수 있습니다.
흥미롭게도, 중성 종의 활성 계수는 리터당 0.1 몰 미만의 이온 강도에서 거의 통일성입니다.
활성 계수와 이온 강도 사이의 관계는 확장된 Debye-Hückel 방정식으로 표현됩니다.
그러나 이온 강도가 매우 낮은 매우 희석된 용액의 경우 방정식은 Debye-Hückel 제한 법칙으로 축소됩니다.

열역학: 활동 계수

활성은 용액 내 종의 유효 농도를 측정한 것입니다. 이는 종의 몰 농도와 활성 계수의 곱으로 표현될 수 있습니다. 활동도 계수는 무차원 양이며 용액의 전체 이온 강도에 따라 달라집니다.

활동 계수는 이상적인 행동으로부터의 편차를 측정한 것입니다. 용액의 이온 강도가 최소일 때 이온 종의 활성 계수는 1에 가까워 활성이 몰 농도와 거의 동일해집니다. 이러한 방식은 이상적인 용액의 동작과 매우 유사한 동작을 나타냅니다. 전하를 띠지 않은 분자의 활동도 계수는 0.1mol/L 미만의 모든 이온 강도에서 대략 1입니다.

용액의 이온 강도가 증가하면 활성도 계수가 감소하여 활성도가 몰 농도보다 작아집니다. 이는 이상적인 행동에서 종의 편차를 나타냅니다. 0.1 mol/L보다 높은 이온 강도를 갖는 용액에서는 활동도 계수가 증가하여 1을 초과합니다.

이온 강도로부터 활동도 계수를 계산하는 데 유용한 방정식은 이온 강도, 이온의 유효 직경 및 용질의 이온 전하와 계수를 연결하는 확장된 데바이-휘켈 방정식입니다. 데바이-휘켈 방정식은 이온 크기(수화물 이온의 유효 직경)에 의존합니다. 이는 전하와 이온의 기하학적 구조에 따라 크게 달라질 수 있으므로 방정식에 불확실성이 발생합니다.

이 방정식은 극도로 희석된 용액과 이온 강도가 0.1 mol/L 미만인 용액 및 극도로 희석된 용액에서 잘 작동합니다. 여기서 이온 크기의 불확실성은 활동 계수에 무시할 수 있는 영향을 미칩니다. 이러한 경우 용액은 대부분 이상적으로 작동하며 데바이-휘켈 방정식은 제한 법칙으로 알려진 더 간단한 형태로 축소됩니다.

활동은 효과적인 집중의 척도입니다. 그것은 단위가 없으며 종의 몰 농도와 그 산물로 표현 될 수 있습니다 ...

Education

교육

JoVE Core

Analytical Chemistry

분석 화학

Unit 1

제1단원

Chemical Equilibria

화학 평형

KEY TERMS AND CONCEPTS

주요 용어 및 개념

Thermodynamics: Activity Coefficient

activity coefficient in ionic solutions

Activity coefficient in ionic solutions describes how much a species behaves like its measured concentration. Activity is the effective concentration of a solute in solution. It equals the molar concentration multiplied by the activity coefficient, which is a unitless number.

The activity coefficient depends on the total ionic strength of the solution. It shows how far a solution is from ideal behavior. When ionic strength is very low, the activity coefficient of an ionic species is close to 1, so activity is nearly the same as molar concentration. In that case, the solution behaves much like an ideal solution.

An uncharged molecule has an activity coefficient of about 1 at ionic strengths below 0.1 mol/L. As ionic strength rises, the activity coefficient of a species can decrease, and activity becomes less than the molar concentration. This shift shows greater deviation from ideal behavior. For ionic strengths above 0.1 mol/L, the activity coefficient increases and can exceed 1.

The extended Debye-Hückel equation is used to estimate activity coefficients from ionic strength. It relates the coefficient to ionic strength, the effective diameter of the ion, and the ionic charges of the solute. The equation depends on ion size, which is the effective diameter of a hydrated ion. Ion size can vary with charge and ion geometry, so it adds uncertainty to the calculation.

The Debye-Hückel equation works best in extremely dilute solutions and in solutions with ionic strength below 0.1 mol/L. In these cases, uncertainty in ion size has little effect on the activity coefficient. The solution behaves mostly ideally, and the equation reduces to the simpler Debye-Hückel Limiting Law.

Activity Coefficient in Ionic Solutions

ionic strength: overview

Ionic Strength in Salt and Acid Solutions

Ionic strength describes the total electrolyte concentration in a solution. It is a quantitative measure of how many ions are present and how strongly they contribute to the solution. The concept was introduced in 1921 by Gilbert N. Lewis and Merle Randall while they were describing the activity coefficient of strong electrolytes. To calculate ionic strength, written as I or μ, both cations and anions are included. The concentration of each ion matters, but the charge number z matters even...

ionic strength: effects on chemical equilibria

ionic-strength-effects-on-chemical-equilibria

Salt Effect on Salt Solubility

Salt effect can change the solubility of a sparingly soluble salt in water. When an inert ionic compound is added, the dissolved salt may become more soluble. A common example is potassium nitrate added to a saturated calcium sulfate solution, which increases the amount of calcium sulfate that dissolves. Le Châtelier’s principle does not explain this shift well. Instead, the change is described by the effective concentration of ions in solution. Each ion is surrounded by an ionic atmosphere,...

thermodynamics: chemical potential and activity

thermodynamics-chemical-potential-and-activity

Chemical Potential in Solution Activity

Chemical potential and activity describe how a species behaves in a solution. Activity is the effective concentration of a species. It accounts for the electrolytes near that species and depends on the ionic strength of the solution. Activity is calculated as molar concentration multiplied by the activity coefficient. This makes it a more precise way to describe a species in solution than concentration alone. The thermodynamic equilibrium constant is also defined more accurately using activity...

thermodynamics: activity coefficient

Activity coefficient in ionic solutions describes how much a species behaves like its measured concentration. Activity is the effective concentration of a solute in solution. It equals the molar concentration multiplied by the activity coefficient, which is a unitless number. The activity coefficient depends on the total ionic strength of the solution. It shows how far a solution is from ideal behavior. When ionic strength is very low, the activity coefficient of an ionic species is close to...

chemical equilibria: redefining equilibrium constant

chemical-equilibria-redefining-equilibrium-constant

Salt Effect in Equilibrium Constant Calculations

Salt effect changes how a sparingly soluble salt dissolves when an inert salt is added. The size of this effect depends on the ionic strength of the solution. Ionic strength reflects how strongly the ions in the solution interact. In solution, the activity of a species is the product of its concentration and its activity coefficient. A redefined equilibrium constant must account for these activity effects when the ionic strength is moderately high. This form is also called the thermodynamic...

factors affecting activity coefficient

How Ionic Strength Changes Activity Coefficient

The activity coefficient of an ion in water depends on ionic strength, ion charge, and ion size. The extended Debye-Hückel equation describes these effects for aqueous solutions at 25°C. These three factors are partly linked, so changes in one can influence the others. When a solution has almost zero ionic strength, the activity coefficient is close to one. That means the solution behaves almost ideally. As ionic strength rises from 0 to 0.1 mol/L, the activity coefficient usually drops.

chemical equilibria: systematic approach to equilibrium calculations

chemical-equilibria-systematic-approach-to-equilibrium-calculations

Equilibrium Calculations with Mass and Charge

Chemical equilibrium calculations become easier when they are organized around mass balance and charge balance. This approach is useful for systems with multiple equilibria, where several reactions must be considered together. It is especially helpful when finding the solubility of a sparingly soluble salt in water with a common ion present. The first step is to identify every chemical reaction in the system. Next, write the equilibrium constant expression for each reaction. These expressions...

acid&#8211;base equilibria: activity-based definition of ph

acidbase-equilibria-activity-based-definition-of-ph

How Ionic Strength Changes pH

pH depends on hydrogen ion activity, not just hydrogen ion concentration. In an ideal solution, pH is the negative logarithm of the hydrogen ion concentration. In a non-ideal solution, a more accurate pH uses hydrogen ion activity, which combines concentration with an activity coefficient. This difference matters most in very low ionic strength solutions, such as pure water. At first, the hydrogen ion activity coefficient is close to one. When an electrolyte that does not donate or accept a...

ladder diagrams: acid&#8211;base equilibria

Using Ladder Diagrams to Predict pH

Ladder diagrams help show how acid-base equilibria change with pH. They are graphical tools that make the chemistry of a system easier to read during analysis. In a ladder diagram, the vertical axis shows pH. Horizontal bars, or steps, place the pKa values in the system.

ladder diagrams: redox equilibria

Redox Potential Shifts in Ladder Diagrams

Ladder diagrams show redox equilibrium using electrochemical potential, E, as the vertical scale. They help students see how changes in concentration affect which species is most stable. The areas of predominance are set with the Nernst equation. A useful example is the Fe3+/Fe2+ half-reaction, which has a standard-state potential of +0.771 V. At potentials more positive than +0.771 V, Fe3+ predominates. At potentials more negative than +0.771 V, Fe2+ predominates. Ladder diagrams also show...

ladder diagrams: complexation equilibria

Reading Metal-Ligand Ladder Diagrams

Ladder diagrams help show equilibria in metal-ligand complexes. In these diagrams, the vertical scale shows pL, or the concentration of free ligand that has not reacted. The horizontal lines mark the log of formation constants and show which species is dominant in each region. For the Cd and ammonia system, the formation constant K1 for Cd(NH3)2+ is 3.55 × 10^2. Its log value is 2.55, so pNH3 = 2.55 is the dividing line between Cd2+ and Cd(NH3)2+ dominance. Above 2.55, Cd2+ is the predominant...

solubility equilibria: overview

How Solubility Reaches Equilibrium

Solubility equilibrium describes what happens when a sparingly soluble salt dissolves in water and then reaches a balance with the solid left over. In a saturated solution, dissolved ions and the undissolved solid are in dynamic equilibrium. The process is reversible, so this topic is also called precipitation equilibrium. This balance matters in real life. Sugar-rich foods can produce organic acids that dissolve hydroxyapatite, the mineral in tooth enamel, which can lead to tooth decay. A...

solubility equilibria: ionic product of water

solubility-equilibria-ionic-product-of-water

Water Ionization and Kw in Equilibrium

Water ionization and the ionic product of water describe how pure water reaches equilibrium. Water is a weak electrolyte, so only a small amount breaks into hydrogen ions and hydroxide ions. At a fixed temperature, the amount of undissociated water stays almost constant. Because of this, the ionic product of water is the product of the hydrogen ion concentration and the hydroxide ion concentration. It is written as K w . The square root of K w gives the concentration of each ion in pure water.

complexation equilibria: overview

Stepwise Metal-Ligand Complexation

Stepwise metal-ligand complexation forms coordination compounds when metal ions and ligands share electrons through dative, or coordinate covalent, bonds. In these reactions, the metal ion binds to one or more ligands until its coordination number is reached. This number tells how many bonds form between the metal ion and the ligands. In aqueous solution, many metal ions are already surrounded by water molecules. These species are called aqua complexes. Complexation reactions are described by...

complexation equilibria: the chelate effect

complexation-equilibria-the-chelate-effect

Chelating Ligands and Metal Complex Stability

Metal complexes form when metal atoms or cations interact with ligands in a complexation reaction. These donor-acceptor adducts are central to understanding how metal ions bind in chemistry. Ligands can bind in different ways. A monodentate ligand uses one donor site. A bidentate ligand uses two donor sites, and a polydentate ligand uses more than two. Ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms and forms a five-membered ring. Polydentate ligands can...

complexation equilibria: factors influencing stability of complexes

complexation-equilibria-factors-influencing-stability-of-complexes

Complex Ions: Metal and Ligand Stability

Complex ions form when a metal cation accepts electron pairs from ligands, which are the electron pair donors. The stability of these metal complexes depends mainly on the metal ion and on the ligands attached to it. The metal ion’s size and charge play a major role in stability. As the size of the metal ion increases, complex stability usually decreases when the valency of the metal ion and the ligands stays the same. As the charge on the metal ion increases, complex stability increases. <br...

redox equilibria: overview

Redox Electron Transfer and Half-Reactions

Redox reactions involve the transfer of electrons from one species to another. In this type of reaction, electrons are not shared between atoms. They move from the species that loses them to the species that gains them. The species that loses electrons is the reducing agent, also called the reductant. It is oxidized during the reaction. The species that gains electrons is the oxidizing agent, or oxidant, and it is reduced. Redox reactions are often written as two half-reactions. One...

titrimetric methods: types and commonly used strategies

titrimetric-methods-types-and-commonly-used-strategies

Direct, Back, and Displacement Titrations

Titrimetric methods use a standard solution to measure the amount of an analyte in chemistry. The main categories are volumetric, gravimetric, and coulometric methods. Each one reaches the endpoint in a different way. In volumetric titrations, the key measurement is the volume of a titrant with a known concentration. The titrant is added until it reacts completely with the analyte. In gravimetric titrations, the standard solution forms an insoluble precipitate with the analyte. That solid is...

classification of titrimetric analysis based on reaction types

classification-of-titrimetric-analysis-based-on-reaction-types

Four Reaction Types in Titrimetric Analysis

Titrimetric analysis measures solution volume and is also called volumetric analysis. A standard solution with a known concentration is placed in the burette and is called the titrant. The solution with an unknown concentration in the flask is the analyte, or titrand. Titrimetric analysis is grouped into four types based on the reaction between the titrant and the analyte. Acid-base titrations involve a neutralization reaction between an acid and a base. This reaction forms water molecules.

key terms and concepts

Learn how activity coefficient changes with ionic strength, why activity differs from concentration, and when the Debye-Hückel Limiting Law applies.

Activity Coefficient in Ionic Solutions | 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.

Activity Coefficient in Ionic Solutions

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