Surfactants are compounds that lower the surface tension
(or interfacial tension) between two liquids, between a gas and a liquid, or between a liquid and a solid. Surfactants may act as detergent
, foaming agent
s, or dispersant
The word "surfactant" is a blend
of ''surface-active agent'',
Agents that increase surface tension are "surface active" in the literal sense but are not called surfactants since their effect is opposite to the common meaning. A common example of surface tension increase is salting out
: by adding an inorganic salt to an aqueous solution of a weakly polar substance, the substance will precipitate. The substance may itself be a surfactant - this is one of the reasons why many surfactants are ineffective in sea water.
diagram of a micelle
– the lipophilic
tails of the surfactant ions remain inside the oil because they interact more strongly with oil than with water. The polar
"heads" of the surfactant molecules coating the micelle interact more strongly with water, so they form a hydrophilic
outer layer that forms a barrier between micelles. This inhibits the oil droplets, the hydrophobic cores of micelles, from merging into fewer, larger droplets ("emulsion breaking") of the micelle. The compounds that coat a micelle are typically amphiphilic
in nature, meaning that micelles may be stable either as droplets of aprotic
solvents such as oil in water, or as protic solvents such as water in oil. When the droplet is aprotic it is sometimes known as a reverse micelle.]]
Composition and structure
Surfactants are usually organic compound
s that are amphiphilic
, meaning they contain both hydrophobic
groups (their ''tails'') and hydrophilic
groups (their ''heads'').
Therefore, a surfactant contains both a water-insoluble (or oil-soluble) component and a water-soluble component. Surfactants will diffuse in water and adsorb
between air and water or at the interface between oil and water, in the case where water is mixed with oil. The water-insoluble hydrophobic group may extend out of the bulk water phase, into the air or into the oil phase, while the water-soluble head group remains in the water phase.
World production of surfactants is estimated at 15 million tons per year, of which about half are soap
s. Other surfactants produced on a particularly large scale are linear alkylbenzene sulfonates
(1.7 million tons/y), lignin sulfonate
s (600,000 tons/y), fatty alcohol ethoxylate
s (700,000 tons/y), and alkylphenol ethoxylate
s (500,000 tons/y).
[Kurt Kosswig "Surfactants" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, 2005, Weinheim. ]
thumb|alt=Sodium dodecylbenzenesulfonate|4-(5-Dodecyl) benzenesulfonate, a linear dodecylbenzenesulfonate, one of the most common surfactants
Structure of surfactant phases in water
In the bulk aqueous phase, surfactants form aggregates, such as micelles
, where the hydrophobic tails form the core of the aggregate and the hydrophilic heads are in contact with the surrounding liquid. Other types of aggregates can also be formed, such as spherical or cylindrical micelles or lipid bilayer
s. The shape of the aggregates depends on the chemical structure of the surfactants, namely the balance in size between the hydrophilic head and hydrophobic tail. A measure of this is the hydrophilic-lipophilic balance
(HLB). Surfactants reduce the surface tension
of water by adsorbing
at the liquid-air interface. The relation that links the surface tension and the surface excess is known as the Gibbs isotherm
Dynamics of surfactants at interfaces
The dynamics of surfactant adsorption is of great importance for practical applications such as in foaming, emulsifying or coating processes, where bubbles or drops are rapidly generated and need to be stabilized. The dynamics of absorption depend on the diffusion coefficient
of the surfactant. As the interface is created, the adsorption is limited by the diffusion of the surfactant to the interface. In some cases, there can exist an energetic barrier to adsorption or desorption of the surfactant. If such a barrier limits the adsorption rate, the dynamics are said to be ‘kinetically limited'. Such energy barriers can be due to steric
or electrostatic repulsions
The surface rheology
of surfactant layers, including the elasticity and viscosity of the layer, play an important role in the stability of foams and emulsions.
Characterization of interfaces and surfactant layers
Interfacial and surface tension can be characterized by classical methods such as the
-pendant or spinning drop method
Dynamic surface tensions, i.e. surface tension as a function of time, can be obtained by the maximum bubble pressure apparatus
The structure of surfactant layers can be studied by ellipsometry
or X-ray reflectivity
Surface rheology can be characterized by the oscillating drop method or shear surface rheometers such as double-cone, double-ring or magnetic rod shear surface rheometer.
Surfactants in biology
, found in lecithin, is a pervasive biological surfactant. Shown in – [[choline and [[phosphate]] group; – [[glycerol]]; – [[monounsaturated fatty acid]]; – [[saturated fatty acid]].]]
The human body produces diverse surfactants. [[Pulmonary surfactant]] is produced in the [[lung]]s in order to facilitate breathing by increasing total lung capacity
, and lung compliance
. In respiratory distress syndrome
or RDS, surfactant replacement
therapy helps patients have normal respiration by using pharmaceutical forms of the surfactants. One example of pharmaceutical pulmonary surfactants is Survanta (beractant
) or its generic form Beraksurf produced by Abbvie
respectively. Bile salts
, a surfactant produced in the liver, play an important role in digestion.
Safety and environmental risks
Most anionic and non-ionic surfactants are non-toxic, having LD50
comparable to sodium chloride. The toxicity of quaternary ammonium compounds
, which are antibacterial
, varies. Dialkyldimethylammonium chlorides (DDAC
) used as fabric softener
s have low LD50 (5 g/kg) and are essentially non-toxic, while the disinfectant
alkylbenzyldimethylammonium chloride has an LD50 of 0.35 g/kg. Prolonged exposure to surfactants can irritate and damage the skin because surfactants disrupt the lipid membrane
that protects skin and other cells. Skin irritancy generally increases in the series non-ionic, amphoteric, anionic, cationic surfactants.
Surfactants are routinely deposited in numerous ways on land and into water systems, whether as part of an intended process or as industrial and household waste.]
Anionic surfactants can be found in soils as the result of sewage sludge application, wastewater irrigation, and remediation processes. Relatively high concentrations of surfactants together with multimetals can represent an environmental risk. At low concentrations, surfactant application is unlikely to have a significant effect on trace metal mobility.
In the case of the Deepwater Horizon oil spill, unprecedented amounts of Corexit were sprayed directly into the ocean at the leak and on the sea-water's surface. The apparent theory being that the surfactants isolate droplets of oil, making it easier for petroleum-consuming microbes to digest the oil. The active ingredient in Corexit is dioctyl sodium sulfosuccinate (DOSS), sorbitan monooleate (Span 80), and polyoxyethylenated sorbitan monooleate (Tween-80).
Because of the volume of surfactants released into the environment, their biodegradation is of great interest. Strategies to enhance degradation include ozone treatment and biodegradation. Two major surfactants, linear alkylbenzene sulfonates (LAS) and the alkyl phenol ethoxylates (APE) break down under aerobic conditions found in sewage treatment plants and in soil to nonylphenol, which is thought to be an endocrine disruptor.
[Mergel, Maria. "Nonylphenol and Nonylphenol Ethoxylates." Toxipedia.org. N.p., 1 Nov. 2011. Web. 27 Apr. 2014.] Interest in biodegradable surfactants has led to much interest in "biosurfactants" such as those derived from amino acids.
Attracting much attention is the non-biodegradability of fluorosurfactant, e.g. perfluorooctanoic acid (PFOA).
The annual global production of surfactants was 13 million tonnes in 2008. In 2014, the world market for surfactants reached a volume of more than US$33 billion. Market researchers expect annual revenues to increase by 2.5% per year to around $40.4 billion until 2022. The commercially most significant type of surfactants is currently the anionic surfactant LAS, which is widely used in cleaners and detergents.
Surfactants play an important role as cleaning, wetting, dispersing, emulsifying, foaming and anti-foaming agents in many practical applications and products, including detergents, fabric softeners, motor oils, emulsions, soaps, paints, adhesives, inks, anti-fogs, ski waxes, snowboard wax, deinking of recycled papers, in flotation, washing and enzymatic processes, and laxatives. Also agrochemical formulations such as herbicides (some), insecticides, biocides (sanitizers), and spermicides (nonoxynol-9). Personal care products such as cosmetics, shampoos, shower gel, hair conditioners, and toothpastes. Surfactants are used in firefighting and pipelines (liquid drag reducing agents). Alkali surfactant polymers are used to mobilize oil in oil wells.
The displacement of air from the matrix of cotton pads and bandages so that medicinal solutions can be absorbed for application to various body areas; the displacement of dirt and debris by the use of detergents in the washing of wounds; and the application of medicinal lotions and sprays to surface of skin and mucous membranes.
Detergents in biochemistry and biotechnology
In solution, detergents help solubilize a variety of chemical species by dissociating aggregates and unfolding proteins. Popular surfactants in the biochemistry laboratory are sodium lauryl sulfate (SDS) and cetyl trimethylammonium bromide (CTAB). Detergents are key reagents to extract protein by lysis of the cells and tissues: They disorganize the membrane's lipid bilayer (SDS, Triton X-100, X-114, CHAPS, DOC, and NP-40), and solubilize proteins. Milder detergents such as octyl thioglucoside, octyl glucoside or dodecyl maltoside are used to solubilize membrane proteins such as enzymes and receptors without denaturing them. Non-solubilized material is harvested by centrifugation or other means. For electrophoresis, for example, proteins are classically treated with SDS to denature the native tertiary and quaternary structures, allowing the separation of proteins according to their molecular weight.
Detergents have also been used to decellularise organs. This process maintains a matrix of proteins that preserves the structure of the organ and often the microvascular network. The process has been successfully used to prepare organs such as the liver and heart for transplant in rats. Pulmonary surfactants are also naturally secreted by type II cells of the lung alveoli in mammals.
Quantum dot preparation
Surfactants are used with quantum dots in order to manipulate the growth, assembly, and electrical properties of quantum dots, in addition to mediating reactions on their surfaces. Research is ongoing in how surfactants arrange on the surface of the quantum dots.
Surfactants in droplet-based microfluidics
Surfactants play an important role in droplet-based microfluidics in the stabilization of the droplets, and the prevention of the fusion of droplets during incubation.
The "tails" of most surfactants are fairly similar, consisting of a hydrocarbon chain, which can be branched, linear, or aromatic. Fluorosurfactants have fluorocarbon chains. Siloxane surfactants have siloxane chains.
Many important surfactants include a polyether chain terminating in a highly polar anionic group. The polyether groups often comprise ethoxylated (polyethylene oxide-like) sequences inserted to increase the hydrophilic character of a surfactant. Polypropylene oxides conversely, may be inserted to increase the lipophilic character of a surfactant.
Surfactant molecules have either one tail or two; those with two tails are said to be ''double-chained''.
Most commonly, surfactants are classified according to polar head group. A non-ionic surfactant has no charged groups in its head. The head of an ionic surfactant carries a net positive, or negative charge. If the charge is negative, the surfactant is more specifically called anionic; if the charge is positive, it is called cationic. If a surfactant contains a head with two oppositely charged groups, it is termed zwitterionic. Commonly encountered surfactants of each type include:
Anionic: sulfate, sulfonate, and phosphate, carboxylate derivatives
Anionic surfactants contain anionic functional groups at their head, such as sulfate, sulfonate, phosphate, and carboxylates.
Prominent alkyl sulfates include ammonium lauryl sulfate, sodium lauryl sulfate (sodium dodecyl sulfate, SLS, or SDS), and the related alkyl-ether sulfates sodium laureth sulfate (sodium lauryl ether sulfate or SLES), and sodium myreth sulfate.
*Docusate (dioctyl sodium sulfosuccinate)
* Alkyl-aryl ether phosphates
* Alkyl ether phosphates
Carboxylates are the most common surfactants and comprise the carboxylate salts (soaps), such as sodium stearate. More specialized species include sodium lauroyl sarcosinate and carboxylate-based fluorosurfactants such as perfluorononanoate, perfluorooctanoate (PFOA or PFO).
Cationic head groups
pH-dependent primary, secondary, or tertiary amines; primary and secondary amines become positively charged at pH < 10: octenidine dihydrochloride.
Permanently charged quaternary ammonium salts: cetrimonium bromide (CTAB), cetylpyridinium chloride (CPC), benzalkonium chloride (BAC), benzethonium chloride (BZT), dimethyldioctadecylammonium chloride, and dioctadecyldimethylammonium bromide (DODAB).
Zwitterionic (amphoteric) surfactants have both cationic and anionic centers attached to the same molecule. The cationic part is based on primary, secondary, or tertiary amines or quaternary ammonium cations. The anionic part can be more variable and include sulfonates, as in the sultaines CHAPS (3-3-cholamidopropyl)dimethylammonio1-propanesulfonate) and cocamidopropyl hydroxysultaine. Betaines such as cocamidopropyl betaine have a carboxylate with the ammonium. The most common biological zwitterionic surfactants have a phosphate anion with an amine or ammonium, such as the phospholipids phosphatidylserine, phosphatidylethanolamine, phosphatidylcholine, and sphingomyelins.
Lauryldimethylamine oxide and myristamine oxide are two commonly used zwitterionic surfactants of the tertiary amine oxides structural type.
Non-ionic surfactants have covalently bonded oxygen-containing hydrophilic groups, which are bonded to hydrophobic parent structures. The water-solubility of the oxygen groups is the result of hydrogen bonding. Hydrogen bonding decreases with increasing temperature, and the water solubility of non-ionic surfactants therefore decreases with increasing temperature.
Non-ionic surfactants are less sensitive to water hardness than anionic surfactants, and they foam less strongly. The differences between the individual types of non-ionic surfactants are slight, and the choice is primarily governed having regard to the costs of special properties (e.g., effectiveness and efficiency, toxicity, dermatological compatibility, biodegradability) or permission for use in food.
= Fatty alcohol ethoxylates
* Narrow-range ethoxylate
* Octaethylene glycol monododecyl ether
* Pentaethylene glycol monododecyl ether
= Alkylphenol ethoxylates (APEs or APEOs)
* Triton X-100
= Fatty acid ethoxylates
Fatty acid ethoxylates are a class of very versatile surfactants, which combine in a single molecule the characteristic of a weakly anionic, pH-responsive head group with the presence of stabilizing and temperature responsive ethyleneoxide units.
= Special ethoxylated fatty esters and oils
= Ethoxylated amines and/or fatty acid amides
* Polyethoxylated tallow amine
* Cocamide monoethanolamine
* Cocamide diethanolamine
= Terminally blocked ethoxylates
Fatty acid esters of polyhydroxy compounds
= Fatty acid esters of glycerol
* Glycerol monostearate
* Glycerol monolaurate
= Fatty acid esters of sorbitol
* Sorbitan monolaurate
* Sorbitan monostearate
* Sorbitan tristearate
* Tween 20
* Tween 40
* Tween 60
* Tween 80
= Fatty acid esters of sucrose
= Alkyl polyglucosides
* Decyl glucoside
* Lauryl glucoside
* Octyl glucoside
* , an assay that indicates anionic surfactants in water with a bluing reaction.
Category:Cleaning product components
Category:Underwater diving physics