Electrospray

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The name electrospray is used for an apparatus that employs electricity to disperse a liquid or for the fine aerosol resulting from this process. High voltage is applied to a liquid supplied through an emitter (usually a glass or metallic capillary). Ideally the liquid reaching the emitter tip forms a Taylor cone, which emits a liquid jet through its apex. Varicose waves on the surface of the jet lead to the formation of small and highly charged liquid droplets, which are radially dispersed due to Coulomb repulsion.

Contents

History

In the late 16th century William Gilbert [1] set out to describe the behaviour of magnetic and electrostatic phenomena. He observed that, in the presence of a charged piece of amber, a drop of water deformed into a cone. This effect is clearly related to electrosprays, even though Gilbert did not record any observation related to liquid dispersion under the effect of the electric field.

In 1750 the French clergyman and physicist Jean-Antoine (Abbé) Nollet noted water flowing from a vessel would aerosolize if the vessel was electrified and placed near electrical ground. [2]

In 1882, Lord Rayleigh theoretically estimated the maximum amount of charge a liquid droplet could carry; [3] this is now known as the "Rayleigh limit". His prediction that a droplet reaching this limit would throw out fine jets of liquid was confirmed experimentally more than 100 years later. [4]

In 1914, John Zeleny published work on the behaviour of fluid droplets at the end of glass capillaries. [5] This report presents experimental evidence for several electrospray operating regimes (dripping, burst, pulsating, and cone-jet). A few years later, Zeleny captured the first time-lapse images of the dynamic liquid meniscus. [6]

Between 1964 and 1969 Sir Geoffrey Ingram Taylor produced the theoretical underpinning of electrospraying. [7] [8] [9] Taylor modeled the shape of the cone formed by the fluid droplet under the effect of an electric field; this characteristic droplet shape is now known as the Taylor cone. He further worked with J. R. Melcher to develop the "leaky dielectric model" for conducting fluids. [10]

The number of publications about electrospray started rising significantly around 1990 (as shown in the figure on the right) when John Fenn (2002 Nobel Prize in Chemistry) and others discovered electrospray ionization for mass spectrometry.

log(N+1) number of publications about electrospray by year: patent families from Questel-Orbit, non-patents from Web of Science and from SciFinder-N. ElectroSpray-ByYear.png
log(N+1) number of publications about electrospray by year: patent families from Questel-Orbit, non-patents from Web of Science and from SciFinder-N.

Mechanism

A close-up of an electrospray device, with emitter tip in foreground pointing to the right. The jet of ionised spray is visible within the image. Electrospray close-up.JPG
A close-up of an electrospray device, with emitter tip in foreground pointing to the right. The jet of ionised spray is visible within the image.

To simplify the discussion, the following paragraphs will address the case of a positive electrospray with the high voltage applied to a metallic emitter. A classical electrospray setup is considered, with the emitter situated at a distance from a grounded counter-electrode. The liquid being sprayed is characterized by its viscosity , surface tension , conductivity , and relative permittivity .

Effect of small electric fields on liquid menisci

Under the effect of surface tension, the liquid meniscus assumes a semi-spherical shape at the tip of the emitter. Application of the positive voltage will induce the electric field: [11]

where is the liquid radius of curvature. This field leads to liquid polarization: the negative/positive charge carriers migrate toward/away from the electrode where the voltage is applied. At voltages below a certain threshold, the liquid quickly reaches a new equilibrium geometry with a smaller radius of curvature.

The Taylor cone

Voltages above the threshold draw the liquid into a cone. Sir Geoffrey Ingram Taylor described the theoretical shape of this cone based on the assumptions that (1) the surface of the cone is an equipotential surface and (2) the cone exists in a steady state equilibrium. [7] To meet both of these criteria the electric field must have azimuthal symmetry and have dependence to balance the surface tension and produce the cone. The solution to this problem is:

where (equipotential surface) exists at a value of (regardless of R) producing an equipotential cone. The magic angle necessary for for all R is a zero of the Legendre polynomial of order 1/2, . There is only one zero between 0 and at 130.7099°, which is the complement of the Taylor's now famous 49.3° angle.

Singularity development

The apex of the conical meniscus cannot become infinitely small. A singularity develops when the hydrodynamic relaxation time becomes larger than the charge relaxation time . [12] The undefined symbols stand for characteristic length and vacuum permittivity . Due to intrinsic varicose instability, the charged liquid jet ejected through the cone apex breaks into small charged droplets, which are radially dispersed by the space-charge.

Closing the electrical circuit

The charged liquid is ejected through the cone apex and captured on the counter electrode as charged droplets or positive ions. To balance the charge loss, the excess negative charge is neutralized electrochemically at the emitter. Imbalances between the amount of charge generated electrochemically and the amount of charge lost at the cone apex can lead to several electrospray operating regimes. For cone-jet electrosprays, the potential at the metal/liquid interface self-regulates to generate the same amount of charge as that lost through the cone apex. [13]

Applications

Electrospray ionization

Electrospray became widely used as ionization source for mass spectrometry after the Fenn group successfully demonstrated its use as ion source for the analysis of large biomolecules. [14]

Liquid metal ion source

A liquid metal ion source (LMIS) uses electrospray in conjunction with liquid metal to form ions. [15] [16] Ions are produced by field evaporation at tip of the Taylor cone. Ions from a LMIS are used in ion implantation and in focused ion beam instruments.

Electrospinning

Similarly to the standard electrospray, the application of high voltage to a polymer solution can result in the formation of a cone-jet geometry. If the jet turns into very fine fibers instead of breaking into small droplets, the process is known as electrospinning .

Colloid thrusters

Electrospray techniques are used as low thrust electric propulsion rocket engines to control satellites, since the fine-controllable particle ejection allows precise and effective thrust.

Deposition of particles for nanostructures

Electrospray may be used in nanotechnology, [17] for example to deposit single particles on surfaces. This is done by spraying colloids on average containing only one particle per droplet. The solvent evaporates, leaving an aerosol stream of single particles of the desired type. The ionizing property of the process is not crucial for the application but may be used in electrostatic precipitation of the particles.

Deposition of ions as precursors for nanoparticles and nanostructures

Instead of depositing nanoparticles, nanoparticles and nano structures can also fabricated in situ by depositing metal ions to desired locations. Electrochemical reduction of ions to atoms and in situ assembly was believed to be the mechanism of nano structure formation.

Fabrication of drug carriers

Electrospray has garnered attention in the field of drug delivery, and it has been used to fabricate drug carriers including polymer microparticles used in immunotherapy [18] as well as lipoplexes used for nucleic acid delivery. [19] The sub-micrometer-sized drug particles created by electrospray possess increased dissolution rates, thus increased bioavailability due to the increased surface area. [20] The side-effects of drugs can thus be reduced, as smaller dosage is enough for the same effect.

Air purifiers

Electrospray is used in some air purifiers. Particulate suspended in air can be charged by aerosol electrospray, manipulated by an electric field, and collected on a grounded electrode. This approach minimizes the production of ozone which is common to other types of air purifiers.

See also

Related Research Articles

Field-emission electric propulsion (FEEP) is an advanced electrostatic space propulsion concept, a form of ion thruster, that uses a liquid metal as a propellant – usually either caesium, indium, or mercury.

<span class="mw-page-title-main">Mass spectrometry</span> Analytical technique based on determining mass to charge ratio of ions

Mass spectrometry (MS) is an analytical technique that is used to measure the mass-to-charge ratio of ions. The results are presented as a mass spectrum, a plot of intensity as a function of the mass-to-charge ratio. Mass spectrometry is used in many different fields and is applied to pure samples as well as complex mixtures.

<span class="mw-page-title-main">Ion source</span> Device that creates charged atoms and molecules (ions)

An ion source is a device that creates atomic and molecular ions. Ion sources are used to form ions for mass spectrometers, optical emission spectrometers, particle accelerators, ion implanters and ion engines.

<span class="mw-page-title-main">Electrospray ionization</span> Technique used in mass spectroscopy

Electrospray ionization (ESI) is a technique used in mass spectrometry to produce ions using an electrospray in which a high voltage is applied to a liquid to create an aerosol. It is especially useful in producing ions from macromolecules because it overcomes the propensity of these molecules to fragment when ionized. ESI is different from other ionization processes since it may produce multiple-charged ions, effectively extending the mass range of the analyser to accommodate the kDa-MDa orders of magnitude observed in proteins and their associated polypeptide fragments.

<span class="mw-page-title-main">Glow discharge</span> Plasma formed by passage of current through gas

A glow discharge is a plasma formed by the passage of electric current through a gas. It is often created by applying a voltage between two electrodes in a glass tube containing a low-pressure gas. When the voltage exceeds a value called the striking voltage, the gas ionization becomes self-sustaining, and the tube glows with a colored light. The color depends on the gas used.

<span class="mw-page-title-main">Electrohydrodynamics</span> Study of electrically conducting fluids in the presence of electric fields

Electrohydrodynamics (EHD), also known as electro-fluid-dynamics (EFD) or electrokinetics, is the study of the dynamics of electrically charged fluids. It is the study of the motions of ionized particles or molecules and their interactions with electric fields and the surrounding fluid. The term may be considered to be synonymous with the rather elaborate electrostrictive hydrodynamics. ESHD covers the following types of particle and fluid transport mechanisms: electrophoresis, electrokinesis, dielectrophoresis, electro-osmosis, and electrorotation. In general, the phenomena relate to the direct conversion of electrical energy into kinetic energy, and vice versa.

<span class="mw-page-title-main">Vaneless ion wind generator</span>

A vaneless ion wind generator or power fence is a device that generates electrical energy by using the wind to move charged particles across an electric field.

<span class="mw-page-title-main">Ion trap</span> Device for trapping charged particles

An ion trap is a combination of electric and/or magnetic fields used to capture charged particles — known as ions — often in a system isolated from an external environment. Atomic and molecular ion traps have a number of applications in physics and chemistry such as precision mass spectrometry, improved atomic frequency standards, and quantum computing. In comparison to neutral atom traps, ion traps have deeper trapping potentials that do not depend on the internal electronic structure of a trapped ion. This makes ion traps more suitable for the study of light interactions with single atomic systems. The two most popular types of ion traps are the Penning trap, which forms a potential via a combination of static electric and magnetic fields, and the Paul trap which forms a potential via a combination of static and oscillating electric fields.

<span class="mw-page-title-main">Taylor cone</span> Shape formed in electrospraying

A Taylor cone refers to the cone observed in electrospinning, electrospraying and hydrodynamic spray processes from which a jet of charged particles emanates above a threshold voltage. Aside from electrospray ionization in mass spectrometry, the Taylor cone is important in field-emission electric propulsion (FEEP) and colloid thrusters used in fine control and high efficiency thrust of spacecraft.

<span class="mw-page-title-main">Liquid chromatography–mass spectrometry</span> Analytical chemistry technique

Liquid chromatography–mass spectrometry (LC–MS) is an analytical chemistry technique that combines the physical separation capabilities of liquid chromatography with the mass analysis capabilities of mass spectrometry (MS). Coupled chromatography – MS systems are popular in chemical analysis because the individual capabilities of each technique are enhanced synergistically. While liquid chromatography separates mixtures with multiple components, mass spectrometry provides spectral information that may help to identify each separated component. MS is not only sensitive, but provides selective detection, relieving the need for complete chromatographic separation. LC–MS is also appropriate for metabolomics because of its good coverage of a wide range of chemicals. This tandem technique can be used to analyze biochemical, organic, and inorganic compounds commonly found in complex samples of environmental and biological origin. Therefore, LC–MS may be applied in a wide range of sectors including biotechnology, environment monitoring, food processing, and pharmaceutical, agrochemical, and cosmetic industries. Since the early 2000s, LC–MS has also begun to be used in clinical applications.

<span class="mw-page-title-main">History of mass spectrometry</span>

The history of mass spectrometry has its roots in physical and chemical studies regarding the nature of matter. The study of gas discharges in the mid 19th century led to the discovery of anode and cathode rays, which turned out to be positive ions and electrons. Improved capabilities in the separation of these positive ions enabled the discovery of stable isotopes of the elements. The first such discovery was with the element neon, which was shown by mass spectrometry to have at least two stable isotopes: 20Ne and 22Ne. Mass spectrometers were used in the Manhattan Project for the separation of isotopes of uranium necessary to create the atomic bomb.

In mass spectrometry, direct analysis in real time (DART) is an ion source that produces electronically or vibronically excited-state species from gases such as helium, argon, or nitrogen that ionize atmospheric molecules or dopant molecules. The ions generated from atmospheric or dopant molecules undergo ion-molecule reactions with the sample molecules to produce analyte ions. Analytes with low ionization energy may be ionized directly. The DART ionization process can produce positive or negative ions depending on the potential applied to the exit electrode.

<span class="mw-page-title-main">Desorption electrospray ionization</span>

Desorption electrospray ionization (DESI) is an ambient ionization technique that can be coupled to mass spectrometry (MS) for chemical analysis of samples at atmospheric conditions. Coupled ionization sources-MS systems are popular in chemical analysis because the individual capabilities of various sources combined with different MS systems allow for chemical determinations of samples. DESI employs a fast-moving charged solvent stream, at an angle relative to the sample surface, to extract analytes from the surfaces and propel the secondary ions toward the mass analyzer. This tandem technique can be used to analyze forensics analyses, pharmaceuticals, plant tissues, fruits, intact biological tissues, enzyme-substrate complexes, metabolites and polymers. Therefore, DESI-MS may be applied in a wide variety of sectors including food and drug administration, pharmaceuticals, environmental monitoring, and biotechnology.

Sample preparation for mass spectrometry is used for the optimization of a sample for analysis in a mass spectrometer (MS). Each ionization method has certain factors that must be considered for that method to be successful, such as volume, concentration, sample phase, and composition of the analyte solution. Quite possibly the most important consideration in sample preparation is knowing what phase the sample must be in for analysis to be successful. In some cases the analyte itself must be purified before entering the ion source. In other situations, the matrix, or everything in the solution surrounding the analyte, is the most important factor to consider and adjust. Often, sample preparation itself for mass spectrometry can be avoided by coupling mass spectrometry to a chromatography method, or some other form of separation before entering the mass spectrometer. In some cases, the analyte itself must be adjusted so that analysis is possible, such as in protein mass spectrometry, where usually the protein of interest is cleaved into peptides before analysis, either by in-gel digestion or by proteolysis in solution.

<span class="mw-page-title-main">Laser spray ionization</span>

Laser spray ionization refers to one of several methods for creating ions using a laser interacting with a spray of neutral particles or ablating material to create a plume of charged particles. The ions thus formed can be separated by m/z with mass spectrometry. Laser spray is one of several ion sources that can be coupled with liquid chromatography-mass spectrometry for the detection of larger molecules.

<span class="mw-page-title-main">Capillary electrophoresis–mass spectrometry</span>

Capillary electrophoresis–mass spectrometry (CE–MS) is an analytical chemistry technique formed by the combination of the liquid separation process of capillary electrophoresis with mass spectrometry. CE–MS combines advantages of both CE and MS to provide high separation efficiency and molecular mass information in a single analysis. It has high resolving power and sensitivity, requires minimal volume and can analyze at high speed. Ions are typically formed by electrospray ionization, but they can also be formed by matrix-assisted laser desorption/ionization or other ionization techniques. It has applications in basic research in proteomics and quantitative analysis of biomolecules as well as in clinical medicine. Since its introduction in 1987, new developments and applications have made CE-MS a powerful separation and identification technique. Use of CE–MS has increased for protein and peptides analysis and other biomolecules. However, the development of online CE–MS is not without challenges. Understanding of CE, the interface setup, ionization technique and mass detection system is important to tackle problems while coupling capillary electrophoresis to mass spectrometry.

<span class="mw-page-title-main">Ambient ionization</span>

Ambient ionization is a form of ionization in which ions are formed in an ion source outside the mass spectrometer without sample preparation or separation. Ions can be formed by extraction into charged electrospray droplets, thermally desorbed and ionized by chemical ionization, or laser desorbed or ablated and post-ionized before they enter the mass spectrometer.

A liquid metal ion source (LMIS) is an ion source which uses metal that is heated to the liquid state and used to form an electrospray to form ions. An electrospray Taylor cone is formed by the application of a strong electric field and ions are produced by field evaporation at the sharp tip of the cone, which has a high electric field. Ions from a LMIS are used in ion implantation and in focused ion beam instruments. Typically gallium is preferred for its low melting point, low vapor pressure, its relatively unreactive nature, and because the gallium ion is sufficiently heavy for ion milling.

<span class="mw-page-title-main">Ion funnel</span>

In mass spectrometry, an ion funnel is a device used to focus a beam of ions using a series of stacked ring electrodes with decreasing inner diameter. A combined radio frequency and fixed electrical potential is applied to the grids. In electrospray ionization-mass spectrometry (ESI-MS), ions are created at atmospheric pressure, but are analyzed at subsequently lower pressures. Ions can be lost while they are shuttled from areas of higher to lower pressure due to the transmission process caused by a phenomenon called joule expansion or “free-jet expansion.” These ion clouds expand outward, which limits the amount of ions that reach the detector, so fewer ions are analyzed. The ion funnel refocuses and transmits ions efficiently from those areas of high to low pressure.

Probe electrospray ionization (PESI) is an electrospray-based ambient ionization technique which is coupled with mass spectrometry for sample analysis. Unlike traditional mass spectrometry ion sources which must be maintained in a vacuum, ambient ionization techniques permit sample ionization under ambient conditions, allowing for the high-throughput analysis of samples in their native state, often with minimal or no sample pre-treatment. The PESI ion source simply consists of a needle to which a high voltage is applied following sample pick-up, initiating electrospray directly from the solid needle.

References

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