Hubbry Logo
ElectrolyteElectrolyteMain
Open search
Electrolyte
Community hub
Electrolyte
logo
7 pages, 0 posts
0 subscribers
Be the first to start a discussion here.
Be the first to start a discussion here.
Electrolyte
Electrolyte
from Wikipedia

An electrolyte is a substance that conducts electricity through the movement of ions, but not through the movement of electrons.[1][2][3] This includes most soluble salts, acids, and bases, dissolved in a polar solvent like water. Upon dissolving, the substance separates into cations and anions, which disperse uniformly throughout the solvent.[4] Solid-state electrolytes also exist. In medicine and sometimes in chemistry, the term electrolyte refers to the substance that is dissolved.[5][6]

Electrically, such a solution is neutral. If an electric potential is applied to such a solution, the cations of the solution are drawn to the electrode that has an abundance of electrons, while the anions are drawn to the electrode that has a deficit of electrons. The movement of anions and cations in opposite directions within the solution amounts to a current. Some gases, such as hydrogen chloride (HCl), under conditions of high temperature or low pressure can also function as electrolytes.[clarification needed] Electrolyte solutions can also result from the dissolution of some biological (e.g., DNA, polypeptides) or synthetic polymers (e.g., polystyrene sulfonate), termed "polyelectrolytes", which contain charged functional groups. A substance that dissociates into ions in solution or in the melt acquires the capacity to conduct electricity. Sodium, potassium, chloride, calcium, magnesium, and phosphate in a liquid phase are examples of electrolytes.

In medicine, electrolyte replacement is needed when a person has prolonged vomiting or diarrhea, and as a response to sweating due to strenuous athletic activity. Commercial electrolyte solutions are available, particularly for sick children (such as oral rehydration solution, Suero Oral, or Pedialyte) and athletes (sports drinks). Electrolyte monitoring is important in the treatment of anorexia and bulimia.

In science, electrolytes are one of the main components of electrochemical cells.[2]

In clinical medicine, mentions of electrolytes usually refer metonymically to the ions, and (especially) to their concentrations (in blood, serum, urine, or other fluids). Thus, mentions of electrolyte levels usually refer to the various ion concentrations, not to the fluid volumes.

Etymology

[edit]

The word electrolyte derives from Ancient Greek ήλεκτρο- (ēlectro-), prefix originally meaning amber but in modern contexts related to electricity, and λυτός (lytos), meaning "able to be taken apart".[7]

History

[edit]
Svante Arrhenius, father of the concept of electrolyte dissociation in aqueous solution for which he received the Nobel Prize in Chemistry in 1903

In his 1884 dissertation, Svante Arrhenius put forth his explanation of solid crystalline salts disassociating into paired charged particles when dissolved, for which he won the 1903 Nobel Prize in Chemistry.[8][9][10][11] Arrhenius's explanation was that in forming a solution, the salt dissociates into charged particles, to which Michael Faraday (1791–1867) had given the name "ions" many years earlier. Faraday's belief had been that ions were produced in the process of electrolysis. Arrhenius proposed that, even in the absence of an electric current, solutions of salts contained ions. He thus proposed that chemical reactions in solution were reactions between ions.[9][10][11]

Shortly after Arrhenius's hypothesis of ions, Franz Hofmeister and Siegmund Lewith[12][13][14] found that different ion types displayed different effects on such things as the solubility of proteins. A consistent ordering of these different ions on the magnitude of their effect arises consistently in many other systems as well. This has since become known as the Hofmeister series.

While the origins of these effects are not abundantly clear and have been debated throughout the past century, it has been suggested that the charge density of these ions is important[15] and might actually have explanations originating from the work of Charles-Augustin de Coulomb over 200 years ago.

Formation

[edit]

Electrolyte solutions are normally formed when salt is placed into a solvent such as water and the individual components dissociate due to the thermodynamic interactions between solvent and solute molecules, in a process called "solvation". For example, when table salt (sodium chloride), NaCl, is placed in water, the salt (a solid) dissolves into its component ions, according to the dissociation reaction:[citation needed]

NaCl(s) → Na+(aq) + Cl(aq)

It is also possible for substances to react with water, producing ions. For example, carbon dioxide gas dissolves in water to produce a solution that contains hydronium, carbonate, and hydrogen carbonate ions.[16]

Molten salts can also be electrolytes as, for example, when sodium chloride is molten, the liquid conducts electricity. In particular, ionic liquids, which are molten salts with melting points below 100 °C,[17] are a type of highly conductive non-aqueous electrolytes and thus have found more and more applications in fuel cells and batteries.[18]

An electrolyte in a solution may be described as "concentrated" if it has a high concentration of ions, or "dilute" if it has a low concentration. If a high proportion of the solute dissociates to form free ions, the electrolyte is strong; if most of the solute does not dissociate, the electrolyte is weak. The properties of electrolytes may be exploited using electrolysis to extract constituent elements and compounds contained within the solution.[citation needed]

Alkaline earth metals form hydroxides that are strong electrolytes with limited solubility in water, due to the strong attraction between their constituent ions. This limits their application to situations where high solubility is required.[19]

In 2021, researchers have found that electrolyte can "substantially facilitate electrochemical corrosion studies in less conductive media".[20]

Physiological importance

[edit]

In physiology, the primary ions of electrolytes are sodium (Na+), potassium (K+), calcium (Ca2+), magnesium (Mg2+), chloride (Cl), hydrogen phosphate (HPO42−), and hydrogen carbonate (HCO3).[21][failed verification] The electric charge symbols of plus (+) and minus (−) indicate that the substance is ionic in nature and has an imbalanced distribution of electrons, the result of chemical dissociation. Sodium is the main electrolyte found in extracellular fluid and potassium is the main intracellular electrolyte;[22] both are involved in fluid balance and blood pressure control.[23]

All known multicellular lifeforms require a subtle and complex electrolyte balance between the intracellular and extracellular environments.[21] In particular, the maintenance of precise osmotic gradients of electrolytes is important. Such gradients affect and regulate the hydration of the body as well as blood pH, and are critical for nerve and muscle function. Various mechanisms exist in living species that keep the concentrations of different electrolytes under tight control.[24]

Both muscle tissue and neurons are considered electric tissues of the body. Muscles and neurons are activated by electrolyte activity between the extracellular fluid or interstitial fluid, and intracellular fluid. Electrolytes may enter or leave the cell membrane through specialized protein structures embedded in the plasma membrane called "ion channels". For example, muscle contraction is dependent upon the presence of calcium (Ca2+), sodium (Na+), and potassium (K+). Without sufficient levels of these key electrolytes, muscle weakness or severe muscle contractions may occur.[citation needed][25]

Electrolyte balance is maintained by oral, or in emergencies, intravenous (IV) intake of electrolyte-containing substances, and is regulated by hormones, in general with the kidneys flushing out excess levels. In humans, electrolyte homeostasis is regulated by hormones such as antidiuretic hormones, aldosterone and parathyroid hormones. Serious electrolyte disturbances, such as dehydration and overhydration, may lead to cardiac and neurological complications and, unless they are rapidly resolved, will result in a medical emergency.[citation needed]

Measurement

[edit]

Measurement of electrolytes is a commonly performed diagnostic procedure, performed via blood testing with ion-selective electrodes or urinalysis by medical technologists. The interpretation of these values is somewhat meaningless without analysis of the clinical history and is often impossible without parallel measurements of renal function. The electrolytes measured most often are sodium and potassium. Chloride levels are rarely measured except for arterial blood gas interpretations since they are inherently linked to sodium levels. One important test conducted on urine is the specific gravity test to determine the occurrence of an electrolyte imbalance.[citation needed]

Conductivity cells are another kind of tools used to measure the electrolyte solution's strength to conduct electricity.[26]

Rehydration

[edit]

According to a study paid for by the Gatorade Sports Science Institute, electrolyte drinks containing sodium and potassium salts replenish the body's water and electrolyte concentrations after dehydration caused by exercise, excessive alcohol consumption, diaphoresis (heavy sweating), diarrhea, vomiting, intoxication or starvation; the study says that athletes exercising in extreme conditions (for three or more hours continuously, e.g. a marathon or triathlon) who do not consume electrolytes risk dehydration (or hyponatremia).[27][needs independent confirmation]

A home-made electrolyte drink can be made by using water, sugar and salt in precise proportions.[28] It is important to include glucose (sugar) to utilise the co-transport mechanism of sodium and glucose[clarification needed]. Commercial preparations are also available[29] for both human and veterinary use.

Electrolytes are commonly found in fruit juices, sports drinks, milk, nuts, and many fruits and vegetables (whole or in juice form) (e.g., potatoes, avocados).

Electrochemistry

[edit]

When electrodes are placed in an electrolyte and a voltage is applied, the electrolyte will conduct electricity. Lone electrons normally cannot pass through the electrolyte; instead, a chemical reaction occurs at the cathode, providing electrons to the electrolyte. Another reaction occurs at the anode, consuming electrons from the electrolyte. As a result, a negative charge cloud develops in the electrolyte around the cathode, and a positive charge develops around the anode. The ions in the electrolyte neutralize these charges, enabling the electrons to keep flowing and the reactions to continue.[citation needed]

Electrolytic cell producing chlorine (Cl2) and sodium hydroxide (NaOH) from a solution of common salt

For example, in a solution of ordinary table salt (sodium chloride, NaCl) in water, the cathode reaction will be

2 H2O + 2e → 2 OH + H2

and hydrogen gas will bubble up; the anode reaction is

2 NaCl → 2 Na+ + Cl2 + 2e

and chlorine gas will be liberated into solution where it reacts with the sodium and hydroxyl ions to produce sodium hypochlorite - household bleach. The positively charged sodium ions Na+ will react toward the cathode, neutralizing the negative charge of OH there, and the negatively charged hydroxide ions OH will react toward the anode, neutralizing the positive charge of Na+ there. Without the ions from the electrolyte, the charges around the electrode would slow down continued electron flow; diffusion of H+ and OH through water to the other electrode takes longer than movement of the much more prevalent salt ions. Electrolytes dissociate in water because water molecules are dipoles and the dipoles orient in an energetically favorable manner to solvate the ions.[citation needed]

In other systems, the electrode reactions can involve the metals of the electrodes as well as the ions of the electrolyte.[30]

Electrolytic conductors are used in electronic devices where the chemical reaction at a metal-electrolyte interface yields useful effects.

  • In batteries, two materials with different electron affinities are used as electrodes; electrons flow from one electrode to the other outside of the battery, while inside the battery the circuit is closed by the electrolyte's ions. Here, the electrode reactions convert chemical energy to electrical energy.[31]
  • In some fuel cells, a solid electrolyte or proton conductor connects the plates electrically while keeping the hydrogen and oxygen fuel gases separated.[32]
  • In electroplating tanks, the electrolyte simultaneously deposits metal onto the object to be plated, and electrically connects that object in the circuit.[citation needed]
  • In operation-hours gauges, two thin columns of mercury are separated by a small electrolyte-filled gap, and, as charge is passed through the device, the metal dissolves on one side and plates out on the other, causing the visible gap to slowly move along.[citation needed]
  • In electrolytic capacitors the chemical effect is used to produce an extremely thin dielectric or insulating coating, while the electrolyte layer behaves as one capacitor plate.[citation needed]
  • In some hygrometers the humidity of air is sensed by measuring the conductivity of a nearly dry electrolyte.[citation needed]
  • Hot, softened glass is an electrolytic conductor, and some glass manufacturers keep the glass molten by passing a large current through it.[citation needed]

Solid electrolytes

[edit]

Solid electrolytes can be mostly divided into four groups described below.

Gel electrolytes

[edit]

Gel electrolytes – closely resemble liquid electrolytes. In essence, they are liquids in a flexible lattice framework. Various additives are often applied to increase the conductivity of such systems.[31][33]

Ceramic electrolytes

[edit]

Solid ceramic electrolytes – ions migrate through the ceramic phase by means of vacancies or interstitials within the lattice. There are also glassy-ceramic electrolytes.[citation needed]

Polymer electrolytes

[edit]

Dry polymer electrolytes differ from liquid and gel electrolytes in that salt is dissolved directly into the solid medium. Usually it is a relatively high-dielectric constant polymer (PEO, PMMA, PAN, polyphosphazenes, siloxanes, etc.) and a salt with low lattice energy. In order to increase the mechanical strength and conductivity of such electrolytes, very often composites are made, and inert ceramic phase is introduced. There are two major classes of such electrolytes: polymer-in-ceramic, and ceramic-in-polymer.[34][35][36]

Organic plastic electrolytes

[edit]

Organic ionic plastic crystals – are a type organic salts exhibiting mesophases (i.e. a state of matter intermediate between liquid and solid), in which mobile ions are orientationally or rotationally disordered while their centers are located at the ordered sites in the crystal structure.[32] They have various forms of disorder due to one or more solid–solid phase transitions below the melting point and have therefore plastic properties and good mechanical flexibility as well as an improved electrode-electrolyte interfacial contact. In particular, protic organic ionic plastic crystals (POIPCs),[32] which are solid protic organic salts formed by proton transfer from a Brønsted acid to a Brønsted base and in essence are protic ionic liquids in the molten state, have found to be promising solid-state proton conductors for fuel cells. Examples include 1,2,4-triazolium perfluorobutanesulfonate[32] and imidazolium methanesulfonate.[37]

See also

[edit]

References

[edit]
[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
An electrolyte is a substance that, when dissolved in or another polar , dissociates into positively charged ions (cations) and negatively charged ions (anions), thereby producing a solution capable of conducting . This ionization process is fundamental to the behavior of electrolytes, distinguishing them from nonelectrolytes that do not produce ions. Electrolytes are classified into two main types based on their degree of dissociation in solution: strong electrolytes, which completely ize to yield high concentrations of free s; and weak electrolytes, which partially ize and result in lower concentrations. Nonelectrolytes, by contrast, do not ize appreciably and thus do not conduct . Strong electrolytes include most soluble salts, strong acids (such as and ), and strong bases (such as ), while weak electrolytes encompass weak acids (like acetic acid) and weak bases (such as ). The extent of determines the solution's electrical conductivity, with strong electrolytes exhibiting the highest conductivity due to the mobility of their s. In biological systems, electrolytes play critical roles in maintaining cellular function, including regulating , supporting impulse transmission, enabling muscle contractions, and preserving acid-base equilibrium. Key physiological electrolytes include sodium (Na⁺), potassium (K⁺), chloride (Cl⁻), calcium (Ca²⁺), magnesium (Mg²⁺), (PO₄³⁻), and (HCO₃⁻), which are transported across cell membranes and contribute to electrical signaling in nerves and muscles. Imbalances in these ions can lead to conditions such as or , disrupting . Beyond biology, electrolytes are essential in and technologies, where they facilitate transport between electrodes in batteries and electrolytic cells. In -ion batteries, for instance, electrolytes enable the movement of while providing electrical insulation between the and , directly influencing battery performance, safety, and cycle life. Advances in solid-state and aim to enhance ionic conductivity and stability, addressing limitations in traditional liquid electrolytes.

Introduction

Definition

An electrolyte is a substance that, when dissolved in a such as , dissociates into positively and negatively charged ions called cations and anions, respectively, thereby producing a solution capable of conducting through the movement of these ions. This dissociation is the fundamental characteristic that distinguishes electrolytes from non-electrolytes, which are substances that dissolve to form neutral molecules without producing ions and thus do not conduct in solution. Common examples of electrolytes include (NaCl), which dissociates into Na⁺ and Cl⁻ ions, and (HCl), which ionizes to yield H⁺ and Cl⁻ ions. These ionic species enable the conduction of by allowing ions to migrate under an applied . Electrolytes are not limited to solutions; molten salts, such as fused NaCl, also serve as electrolytes by providing mobile ions without the need for a , facilitating electrical conductivity in the liquid state. The term "electrolyte" was coined by in 1834 to describe substances involved in electrolytic conduction.

Classification

Electrolytes are classified primarily based on their degree of dissociation in solution, which determines their ability to conduct . Strong electrolytes completely dissociate into ions when dissolved in , producing a high concentration of free ions. Examples include salts such as (NaCl), strong acids like (HCl), and strong bases like (NaOH). In contrast, weak electrolytes dissociate only partially, resulting in a of ions and undissociated molecules. Common examples are weak acids such as acetic acid (CH₃COOH) and weak bases like (NH₃). Electrolytes can also be categorized by their chemical composition into inorganic and organic types. Inorganic electrolytes typically consist of salts, mineral acids, and bases derived from non-carbon-based compounds, such as (KCl), (H₂SO₄), and (Ca(OH)₂). These are prevalent in industrial and laboratory applications due to their stability and high ionic yields. Organic electrolytes, on the other hand, incorporate carbon-based structures and are often found in biological systems, including compounds like acetic acid or lactate ions, which play roles in metabolic processes. For contrast, non-electrolytes do not dissociate into s upon dissolution and thus do not conduct electricity; representative examples include sugar (sucrose, C₁₂H₂₂O₁₁) and (CO(NH₂)₂), which remain as intact molecules in solution. The degree of dissociation serves as a key metric for distinguishing electrolyte strength, particularly for weak electrolytes, where it is quantified by the (Kₐ) for acids or base dissociation constant (K_b) for bases. For instance, acetic acid has a Kₐ of 1.8 × 10⁻⁵, indicating limited dissociation (about 1% in 0.1 M solution), while has a K_b of 1.8 × 10⁻⁵, reflecting similarly partial . This classification influences conductivity, with strong electrolytes exhibiting higher conductance due to greater mobility compared to weak ones.

Historical Context

Etymology

The term "electrolyte" was coined by the English physicist and chemist Michael Faraday in 1834, derived from the Greek words ēlektron (ἤλεκτρον), meaning "amber"—a material historically associated with static electricity—and lytos (λυτός), meaning "soluble" or "able to be dissolved." This etymological construction reflected Faraday's intent to describe substances that could be "loosened" or dissociated by electric forces, emphasizing their role in electrical conduction through dissolution. In his seminal 1834 paper published in the Philosophical Transactions of the Royal Society, Faraday introduced the term to denote compounds that undergo decomposition under the influence of an electric current, with their constituent elements separating via the movement of charged particles—what would later be understood as ions. He specifically proposed: "Many bodies are decomposed directly by the electric current, their elements being set free; these I propose to call electrolytes," distinguishing them from other materials in the context of electrolysis experiments. Faraday collaborated with classical scholar William Whewell to refine this and related terminology, ensuring precise linguistic roots for emerging concepts in electrochemistry. Following its introduction, the term "electrolyte" rapidly entered scientific discourse and was adopted internationally with minimal alteration, appearing as électrolyte in French, elettrolita in Italian, and elektrolit in German and Russian by the mid-19th century, reflecting the global standardization of electrochemical . This linguistic consistency facilitated its widespread use in research papers, textbooks, and technical literature, evolving from Faraday's specific electrolytic context to a broader descriptor for ion-conducting media while retaining its original Greek-inspired form.

Key Developments

In the early , advanced the study of electrolytes through his pioneering work on , particularly by decomposing molten salts to isolate new elements. In 1807, Davy successfully isolated and sodium by electrolyzing molten and soda ash, respectively, using a voltaic battery, which demonstrated the potential of electrical decomposition for analyzing ionic compounds. This approach extended to other molten salts, such as those yielding calcium, , , and magnesium in 1808, laying foundational insights into migration in non-aqueous media. Building on Davy's qualitative observations, established quantitative principles in the 1830s through his experimental researches on . In his 1832-1834 publications, Faraday formulated the laws of , stating that the mass of a substance altered at an is directly proportional to the quantity of passed and that the amounts of different substances liberated by a fixed quantity of are proportional to their chemical equivalent weights. These laws provided the first rigorous link between electrical current and transport in electrolytes, enabling precise predictions of electrochemical reactions. A major theoretical breakthrough came in 1887 with Svante Arrhenius's theory of electrolytic dissociation, which posited that electrolytes in solution exist as ions due to partial dissociation of molecules. Arrhenius explained conductivity variations and by proposing that the degree of dissociation increases with dilution, resolving discrepancies in earlier models of solution behavior. This ionic hypothesis, initially controversial, earned Arrhenius the 1903 and became a cornerstone for understanding electrolyte solutions. In the , the Debye-Hückel theory of addressed limitations in Arrhenius's model by accounting for ion-ion interactions in dilute solutions. and Erich Hückel developed a statistical approach treating ions as charged points surrounded by an ionic atmosphere, deriving expressions for activity coefficients that corrected for electrostatic effects on . This theory marked a significant advance in electrolyte , influencing subsequent models of concentrated solutions. Linus Pauling further refined models in the 1930s, integrating with empirical observations to describe the nature of ionic interactions in electrolytes. In his 1939 book The Nature of the Chemical Bond, Pauling introduced scales and rules for ionic crystal structures, predicting coordination geometries based on radius ratios and electrostatic balance, which enhanced understanding of solid electrolytes. These models bridged classical ionic concepts with , providing tools for analyzing lattice energies and in ionic compounds. Post-1950 developments saw the application of (NMR) to probe dynamics in electrolyte solutions, offering molecular-level insights into hydration and coordination. Early NMR studies in the 1960s, such as those examining -solvent interactions in , revealed shifts in proton and cation resonances indicative of specific solvation shells, quantifying exchange rates and binding strengths. This technique, building on the 1950s advent of high-resolution NMR for liquids, enabled real-time observation of dynamic processes in aqueous and non-aqueous electrolytes, advancing research into mobility and .

Chemical Properties

Ion Formation and Dissociation

Electrolytes undergo dissociation in aqueous solutions, wherein the solute molecules or ionic lattices separate into positively and negatively charged , enabling the solution to conduct . For instance, (NaCl) dissociates completely as \ceNaCl>Na++Cl\ce{NaCl -> Na+ + Cl-}, with the sodium cations and anions becoming free to move independently in the . This process involves the heterolytic cleavage of bonds, where the solvent molecules, particularly , stabilize the resulting ions through electrostatic interactions. The foundational explanation for this phenomenon is provided by the Arrhenius theory of electrolytic dissociation, proposed by in 1887. According to this theory, electrolytes such as acids, bases, and salts ionize in to produce free ions that are responsible for both electrical conductivity and chemical reactivity. For strong electrolytes like , the dissociation is nearly complete (e.g., \ceHCl>H++Cl\ce{HCl -> H+ + Cl-}), while weak electrolytes, such as acetic acid, exist in equilibrium (e.g., \ceCH3COOHCH3COO+H+\ce{CH3COOH ⇌ CH3COO- + H+}), where only a fraction of the molecules dissociate. posits that the degree of ionization increases with dilution, approaching full dissociation for strong electrolytes at infinite dilution. Several factors influence the extent of dissociation. The polarity of the solvent plays a crucial role; highly polar solvents like , with a high constant, promote dissociation by effectively screening the electrostatic attractions between , whereas nonpolar solvents like suppress it. Temperature generally increases the degree of dissociation, as the process is often endothermic, enhancing ion separation according to , though the effect is relatively modest. Concentration also affects dissociation: for weak electrolytes, dilution shifts the equilibrium toward greater ionization, following Ostwald's dilution law, where the degree of dissociation rises as concentration decreases. In aqueous media, the dissociated ions are stabilized by solvation, forming hydration shells where water molecules orient around the ions via dipole interactions, with the first shell typically comprising 4–6 water molecules for monovalent ions. This solvation process releases hydration energy, which counteracts the lattice energy—the energy required to overcome the strong ionic bonds in the solid salt crystal lattice. For dissolution to occur, the hydration energy must exceed the lattice energy; for example, in NaCl, the lattice energy is approximately 788 kJ/mol, balanced by the combined hydration energies of Na⁺ and Cl⁻ to favor dissociation. During dissociation, the formation of these ordered hydration shells contributes to an entropic penalty, as water molecules become more restricted, influencing the overall thermodynamics. The degree of dissociation, denoted by α\alpha, quantifies the fraction of electrolyte molecules that have ionized and is defined as α=NdisN\alpha = \frac{N_{\text{dis}}}{N}, where NdisN_{\text{dis}} is the number of dissociated molecules and NN is the initial number of molecules. For a binary electrolyte like NaCl, this simplifies to the ratio of ion concentration to the total electrolyte concentration at equilibrium. Electrolytes are classified as strong if α1\alpha \approx 1 (complete dissociation) or weak if α<1\alpha < 1 (partial dissociation).

Conductivity

Electrolytic conductivity arises from the movement of s in a solution under an applied , where positively charged cations migrate toward the and negatively charged anions toward the , carrying charge and generating current. This process requires prior dissociation in solution, as detailed in related discussions on ion formation. The specific conductance, denoted as κ and measured in per centimeter (S/cm), quantifies this conductivity independent of the solution's , representing the ability of the electrolyte to conduct per unit length and cross-sectional area. A key governing electrolytic conductivity is Kohlrausch's law of the independent migration of s, which states that at infinite dilution, the molar conductivity Λ_m of an electrolyte equals the sum of the ionic conductivities of its constituent s: Λm=λ++λ\Lambda_m = \lambda_+ + \lambda_- where λ_+ and λ_- are the molar ionic conductivities of the cation and anion, respectively. This law highlights that each contributes independently to the total conductivity without interference at very low concentrations, allowing the prediction of limiting molar conductivities for electrolytes based on tabulated ionic values. As electrolyte concentration increases, the molar conductivity of strong electrolytes decreases due to interionic attractions that reduce mobility through electrostatic interactions and relaxation effects. The Debye-Hückel-Onsager provides a theoretical framework for this variation, expressing the as a function of the of concentration: Λm=Λm0(A+BΛm0)c\Lambda_m = \Lambda_m^0 - (A + B\Lambda_m^0)\sqrt{c}
Add your contribution
Related Hubs
User Avatar
No comments yet.