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Monday, June 15, 2026

Superconductivity

From Wikipedia, the free encyclopedia
A high-temperature superconductor levitating above a magnet. A persistent electric current flows on the surface of the superconductor, acting to exclude the magnetic field of the magnet (Meissner effect). This current effectively forms an electromagnet that repels the magnet.

Superconductivity is a set of physical properties observed in superconductors: materials where electrical resistance vanishes and magnetic fields are expelled from the material. Unlike an ordinary metallic conductor, whose resistance decreases gradually as its temperature is lowered, even down to near absolute zero, a superconductor has a characteristic critical temperature below which the resistance drops abruptly to zero. An electric current through a loop of superconducting wire can persist indefinitely with no power source.

The superconductivity phenomenon was discovered in 1911 by Dutch physicist Heike Kamerlingh Onnes. Like ferromagnetism and atomic spectral lines, superconductivity is a phenomenon which can only be explained by quantum mechanics. It is characterized by the Meissner effect, the complete cancellation of the magnetic field in the interior of the superconductor during its transitions into the superconducting state. The occurrence of the Meissner effect indicates that superconductivity cannot be understood simply as the idealization of perfect conductivity in classical physics.

In 1986, it was discovered that some cuprate-perovskite ceramic materials have a critical temperature above 35 K (−238 °C). It was found shortly thereafter (by Ching-Wu Chu) that replacing the lanthanum with yttrium, i.e. making YBCO, raised the critical temperature to 92 K (−181 °C), which was important because liquid nitrogen could then be used as a refrigerant. Such a high transition temperature is theoretically impossible for a conventional superconductor, leading the materials to be termed high-temperature superconductors. The cheaply available coolant liquid nitrogen boils at 77 K (−196 °C) and thus the existence of superconductivity at higher temperatures than this facilitates many experiments and applications that are less practical at lower temperatures.

History

Timeline of superconducting materials. Colors represent different classes of materials:
*NdNiO should read Sr0.2Nd0.8NiO2
Heike Kamerlingh Onnes (right), the discoverer of superconductivity. Paul Ehrenfest, Hendrik Lorentz, Niels Bohr stand to his left.

Superconductivity was discovered in solid mercury on April 8, 1911, by Heike Kamerlingh Onnes, who was studying the resistance of mercury at cryogenic temperatures using the recently produced liquid helium as a refrigerant. At the temperature of 4.2 K, he observed that the resistance abruptly disappeared. In the same experiment, he also observed the superfluid transition of helium at 2.2 K, without recognizing its significance. The precise date and circumstances of the discovery were only reconstructed a century later, when Onnes's notebook was found. In subsequent decades, superconductivity was observed in several other materials. In 1913, Tin and lead were found to superconduct at 3.8K and 7 K respectively, and in 1941 niobium nitride was found to superconduct at 16 K.

Great efforts have been devoted to finding out how and why superconductivity works; the important step occurred in 1933, when Meissner and Ochsenfeld discovered that superconductors expelled applied magnetic fields, a phenomenon which has come to be known as the Meissner effect. In 1935, Fritz and Heinz London showed that the Meissner effect was a consequence of the minimization of the electromagnetic free energy carried by superconducting current.

London constitutive equations

The theoretical model that was first conceived for superconductivity was completely classical: it is summarized by London constitutive equations. It was put forward by the brothers Fritz and Heinz London in 1935, shortly after the discovery that magnetic fields are expelled from superconductors. A major triumph of the equations of this theory is their ability to explain the Meissner effect, wherein a material exponentially expels all internal magnetic fields as it crosses the superconducting threshold. By using the London equation, one can obtain the dependence of the magnetic field inside the superconductor on the distance to the surface.

The two constitutive equations for a superconductor by London are:

The first equation follows from Newton's second law for superconducting electrons.

Conventional theories (1950s)

During the 1950s, theoretical condensed matter physicists arrived at an understanding of "conventional" superconductivity, through a pair of remarkable and important theories: the phenomenological Ginzburg–Landau theory (1950) and the microscopic BCS theory (1957).

In 1950, the phenomenological Ginzburg–Landau theory of superconductivity was devised by Landau and Ginzburg. This theory, which combined Landau's theory of second-order phase transitions with a Schrödinger-like wave equation, had great success in explaining the macroscopic properties of superconductors. In particular, Abrikosov showed that Ginzburg–Landau theory predicts the division of superconductors into the two categories now referred to as Type I and Type II. Abrikosov and Ginzburg were awarded the 2003 Nobel Prize for their work (Landau had received the 1962 Nobel Prize for other work, and died in 1968). The four-dimensional extension of the Ginzburg–Landau theory, the Coleman-Weinberg model, is important in quantum field theory and cosmology.

Also in 1950, Maxwell and Reynolds et al. found that the critical temperature of a superconductor depends on the isotopic mass of the constituent element. This important discovery pointed to the electronphonon interaction as the microscopic mechanism responsible for superconductivity.

The complete microscopic theory of superconductivity was finally proposed in 1957 by Bardeen, Cooper and Schrieffer. This BCS theory explained the superconducting current as a superfluid of Cooper pairs, pairs of electrons interacting through the exchange of phonons. For this work, the authors were awarded the Nobel Prize in 1972.

The BCS theory was set on a firmer footing in 1958, when N. N. Bogolyubov showed that the BCS wavefunction, which had originally been derived from a variational argument, could be obtained using a canonical transformation of the electronic Hamiltonian. In 1959, Lev Gor'kov showed that the BCS theory reduced to the Ginzburg–Landau theory close to the critical temperature.

Generalizations of BCS theory for conventional superconductors form the basis for the understanding of the phenomenon of superfluidity, because they fall into the lambda transition universality class. The extent to which such generalizations can be applied to unconventional superconductors is still controversial.

Niobium

The first practical application of superconductivity was developed in 1954 with Dudley Allen Buck's invention of the cryotron. Two superconductors with greatly different values of the critical magnetic field are combined to produce a fast, simple switch for computer elements.

Soon after discovering superconductivity in 1911, Kamerlingh Onnes attempted to make an electromagnet with superconducting windings but found that relatively low magnetic fields destroyed superconductivity in the materials he investigated. Much later, in 1955, G. B. Yntema succeeded in constructing a small 0.7-tesla iron-core electromagnet with superconducting niobium wire windings. Then, in 1961, J. E. Kunzler, E. Buehler, F. S. L. Hsu, and J. H. Wernick made the startling discovery that, at 4.2 kelvin, niobium–tin, a compound consisting of three parts niobium and one part tin, was capable of supporting a current density of more than 100,000 amperes per square centimeter in a magnetic field of 8.8 tesla. The alloy was brittle and difficult to fabricate, but niobium–tin proved useful for generating magnetic fields as high as 20 tesla.

In 1962, T. G. Berlincourt and R. R. Hake discovered that more ductile alloys of niobium and titanium are suitable for applications up to 10 tesla. Commercial production of niobium–titanium supermagnet wire immediately commenced at Westinghouse Electric Corporation and at Wah Chang Corporation. Although niobium–titanium boasts less-impressive superconducting properties than those of niobium–tin, niobium–titanium became the most widely used "workhorse" supermagnet material, in large measure a consequence of its very high ductility and ease of fabrication. However, both niobium–tin and niobium–titanium found wide application in MRI medical imagers, bending and focusing magnets for enormous high-energy-particle accelerators, and other applications. Conectus, a European superconductivity consortium, estimated that in 2014, global economic activity for which superconductivity was indispensable amounted to about five billion euros, with MRI systems accounting for about 80% of that total.

Josephson effect

In 1962, Josephson made the important theoretical prediction that a supercurrent can flow between two pieces of superconductor separated by a thin layer of insulator. This phenomenon, now called the Josephson effect, is exploited by superconducting devices such as SQUIDs. It is used in the most accurate available measurements of the magnetic flux quantum Φ0 = h/(2e), where h is the Planck constant. Coupled with the quantum Hall resistivity, this leads to a precise measurement of the Planck constant. Josephson was awarded the Nobel Prize for this work in 1973.

In 2008, it was proposed that the same mechanism that produces superconductivity could produce a superinsulator state in some materials, with almost infinite electrical resistance. The first development and study of superconducting Bose–Einstein condensate (BEC) in 2020 suggested a "smooth transition between" BEC and Bardeen-Cooper-Shrieffer regimes.

2D materials

Multiple types of superconductivity are reported in devices made of single-layer materials. Some of these materials can switch between conducting, insulating, and other behaviors.

Twisting materials imbues them with a "moiré" pattern involving tiled hexagonal cells that act like atoms and host electrons. In this environment, the electrons move slowly enough for their collective interactions to guide their behavior. When each cell has a single electron, the electrons take on an antiferromagnetic arrangement; each electron can have a preferred location and magnetic orientation. Their intrinsic magnetic fields tend to alternate between pointing up and down. Adding electrons allows superconductivity by causing Cooper pairs to form. Fu and Schrade argued that electron-on-electron action was allowing both antiferromagnetic and superconducting states.

The first success with 2D materials involved a twisted bilayer graphene sheet (2018, Tc ~1.7 K, 1.1° twist). A twisted three-layer graphene device was later shown to superconduct (2021, Tc ~2.8 K). Then an untwisted trilayer graphene device was reported to superconduct (2022, Tc 1-2 K). The latter was later shown to be tunable, easily reproducing behavior found in millions of other configurations. Directly observing what happens when electrons are added to a material or slightly weakening its electric field enables quick testing of an unprecedented number of recipes to see which lead to superconductivity.

In four and five layer rhombohedral graphene, a form of superconductivity with spontaneously broken time reversal symmetry known as "chiral superconductivity" was recently observed. These systems were not observed to have any superlattice effects, and they can flip between two possible magnetic states without exiting the superconducting phase. This is in strong contrast to other observations of superconductivity and magnetic fields.

These devices have applications in quantum computing.

2D materials other than graphene have also been made to superconduct. Transition metal dichalcogenide (TMD) sheets twisted at 5 degrees intermittently achieved superconduction by creating a Josephson junction. The device used thin layers of palladium to connect to the sides of a tungsten telluride layer surrounded and protected by boron nitride. Another group demonstrated superconduction in molybdenum telluride (MoTe₂) in 2D van der Waals materials using ferroelectric domain walls. The Tc was implied to be higher than typical TMDs (~5–10 K).

A Cornell group added a 3.5-degree twist to an insulator that allowed electrons to slow down and interact strongly, leaving one electron per cell, exhibiting superconduction. Existing theories do not explain this behavior.

Fu and collaborators proposed that electrons arrange to form a repeating crystal that allows the electron grid to float independently of the background atomic nuclei and the electron grid to relax. Its ripples pair electrons the way phonons do, although this is unconfirmed.

Classification

Superconductors are classified according to many criteria. The most common are:

Response to a magnetic field

A superconductor can be Type I, meaning it has a single critical field, above which superconductivity is lost and below which the magnetic field is completely expelled from the superconductor; or Type II, meaning it has two critical fields, between which it allows partial penetration of the magnetic field through isolated points called vortices. Furthermore, in multicomponent superconductors it is possible to combine the two behaviours. In that case the superconductor is of Type-1.5.

Theory of operation

A superconductor is conventional if it is driven by electron–phonon interaction and explained by the BCS theory or its extension, the Eliashberg theory. Otherwise, it is unconventional. Alternatively, a superconductor is called unconventional if the superconducting order parameter transforms according to a non-trivial irreducible representation of the system's point group or space group.

Critical temperature

A superconductor is generally considered high-temperature if it reaches a superconducting state above a temperature of 30 K (−243.15 °C); as in the initial discovery by Georg Bednorz and K. Alex Müller. It may also reference materials that transition to superconductivity when cooled using liquid nitrogen – that is, at only Tc > 77 K, although this is generally used only to emphasize that liquid nitrogen coolant is sufficient. Low temperature superconductors refer to materials with a critical temperature below 30 K, and are cooled mainly by liquid helium (Tc > 4.2 K). One exception to this rule is the iron pnictide group of superconductors that display behaviour and properties typical of high-temperature superconductors, yet some of the group have critical temperatures below 30 K.

Material

Top: Periodic table of superconducting elemental solids and their experimental critical temperature (T)
Bottom: Periodic table of superconducting binary hydrides (0–300 GPa). Theoretical predictions indicated in blue and experimental results in red
Superconductor material classes include

Elementary properties

Several physical properties of superconductors vary from material to material, such as the critical temperature, the value of the superconducting gap, the critical magnetic field, and the critical current density at which superconductivity is destroyed. On the other hand, there is a class of properties that are independent of the underlying material. The Meissner effect, the quantization of the magnetic flux or permanent currents, i.e. the state of zero resistance are the most important examples. The existence of these "universal" properties is rooted in the nature of the broken symmetry of the superconductor and the emergence of off-diagonal long range order. Superconductivity is a thermodynamic phase, and thus possesses certain distinguishing properties which are largely independent of microscopic details. Off diagonal long range order is closely connected to the formation of Cooper pairs.

Zero electrical DC resistance

Electric cables for accelerators at CERN. Both the massive and slim cables are rated for 12,500 A. Top: regular cables for LEP; bottom: superconductor-based cables for the LHC
Cross section of a preformed superconductor rod from the abandoned Texas Superconducting Super Collider (SSC)

The simplest method to measure the electrical resistance of a sample of some material is to place it in an electrical circuit in series with a current source I and measure the resulting voltage V across the sample. The resistance of the sample is given by Ohm's law as R = V / I. If the voltage drop across the sample is zero, this means that the resistance is zero.

Superconductors are also able to maintain a current with no applied voltage whatsoever, a property exploited in superconducting electromagnets such as those found in MRI machines. Experiments have demonstrated that currents in superconducting coils can persist for years without any measurable degradation. Experimental evidence points to a lifetime of at least 100,000 years. Theoretical estimates for the lifetime of a persistent current can exceed the estimated lifetime of the universe, depending on the wire geometry and the temperature. In practice, currents injected in superconducting coils persisted for 28 years, 7 months, 27 days in a superconducting gravimeter in Belgium, from August 4, 1995 until March 31, 2024. In such instruments, the measurement is based on the monitoring of the levitation of a superconducting niobium sphere with a mass of four grams.

In a normal conductor, an electric current may be visualized as a fluid of electrons moving across a heavy ionic lattice. The electrons are constantly colliding with the ions in the lattice, and during each collision some of the energy carried by the current is absorbed by the lattice and converted into heat, which is essentially the vibrational kinetic energy of the lattice ions. As a result, the energy carried by the current is constantly being dissipated. This is the phenomenon of electrical resistance and Joule heating.

The situation is different in a superconductor. In a conventional superconductor, the electronic fluid cannot be resolved into individual electrons. Instead, it consists of bound pairs of electrons known as Cooper pairs. This pairing is caused by an attractive force between electrons from the exchange of phonons. This pairing is very weak, and small thermal vibrations can fracture the bond. Due to quantum mechanics, the energy spectrum of this Cooper pair fluid possesses an energy gap, meaning there is a minimum amount of energy ΔE that must be supplied in order to excite the fluid. Therefore, if ΔE is larger than the thermal energy of the lattice, given by kT, where k is the Boltzmann constant and T is the temperature, the fluid will not be scattered by the lattice. The Cooper pair fluid is thus a superfluid, meaning it can flow without energy dissipation.

In the class of superconductors known as type II superconductors, including all known high-temperature superconductors, an extremely low but non-zero resistivity appears at temperatures not too far below the nominal superconducting transition when an electric current is applied in conjunction with a strong magnetic field, which may be caused by the electric current. This is due to the motion of magnetic vortices in the electronic superfluid, which dissipates some of the energy carried by the current. If the current is sufficiently small, the vortices are stationary, and the resistivity vanishes. The resistance due to this effect is minuscule compared with that of non-superconducting materials, but must be taken into account in sensitive experiments. However, as the temperature decreases far enough below the nominal superconducting transition, these vortices can become frozen into a disordered but stationary phase known as a "vortex glass". Below this vortex glass transition temperature, the resistance of the material becomes truly zero.

Phase transition

Behavior of heat capacity (cv, blue) and resistivity (ρ, green) at the superconducting phase transition

In superconducting materials, the characteristics of superconductivity appear when the temperature T is lowered below a critical temperature Tc. The value of this critical temperature varies from material to material. Conventional superconductors usually have critical temperatures ranging from around 20 K to less than 1 K. Solid mercury, for example, has a critical temperature of 4.2 K. As of 2015, the highest critical temperature found for a conventional superconductor is 203 K for H2S, although high pressures of approximately 90 gigapascals were required. Cuprate superconductors can have much higher critical temperatures: YBa2Cu3O7, one of the first cuprate superconductors to be discovered, has a critical temperature above 90 K, and mercury-based cuprates have been found with critical temperatures in excess of 130 K. The basic physical mechanism responsible for the high critical temperature is not yet clear. However, it is clear that a two-electron pairing is involved, although the nature of the pairing ( wave vs. wave) remains controversial.

Similarly, at a fixed temperature below the critical temperature, superconducting materials cease to superconduct when an external magnetic field is applied which is greater than the critical magnetic field. This is because the Gibbs free energy of the superconducting phase increases quadratically with the magnetic field while the free energy of the normal phase is roughly independent of the magnetic field. If the material superconducts in the absence of a field, then the superconducting phase free energy is lower than that of the normal phase and so for some finite value of the magnetic field (proportional to the square root of the difference of the free energies at zero magnetic field) the two free energies will be equal and a phase transition to the normal phase will occur. More generally, a higher temperature and a stronger magnetic field lead to a smaller fraction of electrons that are superconducting and consequently to a longer London penetration depth of external magnetic fields and currents. The penetration depth becomes infinite at the phase transition.

The onset of superconductivity is accompanied by abrupt changes in various physical properties, which is the hallmark of a phase transition. For example, the electronic heat capacity is proportional to the temperature in the normal (non-superconducting) regime. At the superconducting transition, it suffers a discontinuous jump and thereafter ceases to be linear. At low temperatures, it varies instead as eα/T for some constant, α. This exponential behavior is one of the pieces of evidence for the existence of the energy gap.

The order of the superconducting phase transition was long a matter of debate. Experiments indicate that the transition is second-order, meaning there is no latent heat. However, in the presence of an external magnetic field there is latent heat, because the superconducting phase has a lower entropy below the critical temperature than the normal phase. It has been experimentally demonstrated that, as a consequence, when the magnetic field is increased beyond the critical field, the resulting phase transition leads to a decrease in the temperature of the superconducting material.

Calculations in the 1970s suggested that it may actually be weakly first-order due to the effect of long-range fluctuations in the electromagnetic field. In the 1980s it was shown theoretically with the help of a disorder field theory, in which the vortex lines of the superconductor play a major role, that the transition is of second order within the type II regime and of first order (i.e., latent heat) within the type I regime, and that the two regions are separated by a tricritical point. The results were strongly supported by Monte Carlo computer simulations.

Meissner effect

When a superconductor is placed in a weak external magnetic field Ba=Ha, and cooled below its transition temperature, the magnetic field is ejected. The Meissner effect does not cause the field to be completely ejected but instead, the field penetrates the superconductor but only to a very small distance, characterized by a parameter λ, called the London penetration depth, decaying exponentially to zero within the bulk of the material. The Meissner effect is a defining characteristic of superconductivity. For most superconductors, the London penetration depth is on the order of 100 nm.

The Meissner effect is sometimes confused with the kind of diamagnetism one would expect in a perfect electrical conductor: according to Lenz's law, when a changing magnetic field is applied to a conductor, it will induce an electric current in the conductor that creates an opposing magnetic field. In a perfect conductor, an arbitrarily large current can be induced, and the resulting magnetic field exactly cancels the applied field.

The Meissner effect is distinct from this – it is the spontaneous expulsion that occurs during transition to superconductivity. Suppose we have a material in its normal state, containing a constant internal magnetic field. When the material is cooled below the critical temperature, we would observe the abrupt expulsion of the internal magnetic field, which we would not expect based on Lenz's law.

The Meissner effect was given a phenomenological explanation by the brothers Fritz and Heinz London, who showed that the electromagnetic free energy in a superconductor is minimized provided where B is the magnetic field and λ is the London penetration depth.

This equation, which is known as the London equation, predicts that the magnetic field in a superconductor decays exponentially from whatever value it possesses at the surface.

A superconductor with little or no magnetic field within it is said to be in the Meissner state. The Meissner state breaks down when the applied magnetic field is too large. Superconductors can be divided into two classes according to how this breakdown occurs. In Type I superconductors, superconductivity is abruptly destroyed when the strength of the applied field rises above a critical value Hc. Depending on the geometry of the sample, one may obtain an intermediate state consisting of a baroque pattern of regions of normal material carrying a magnetic field mixed with regions of superconducting material containing no field. In Type II superconductors, raising the applied field past a critical value Hc1 leads to a mixed state (also known as the vortex state) in which an increasing amount of magnetic flux penetrates the material, but there remains no resistance to the flow of electric current as long as the current is not too large. At a second critical field strength Hc2, superconductivity is destroyed. The mixed state is actually caused by vortices in the electronic superfluid, sometimes called fluxons because the flux carried by these vortices is quantized. Most pure elemental superconductors, except niobium and carbon nanotubes, are Type I, while almost all impure and compound superconductors are Type II.

London moment

Conversely, a spinning superconductor generates a magnetic field, precisely aligned with the spin axis. The effect, the London moment, was put to good use in Gravity Probe B. This experiment measured the magnetic fields of four superconducting gyroscopes to determine their spin axes. This was critical to the experiment since it is one of the few ways to accurately determine the spin axis of an otherwise featureless sphere.

High-temperature superconductivity

A sample of bismuth strontium calcium copper oxide (BSCCO), which is currently one of the most practical high-temperature superconductors. Notably, it does not contain rare earths. BSCCO is a cuprate superconductor based on bismuth and strontium. Thanks to its higher operating temperature, cuprates are now becoming competitors for more ordinary niobium-based superconductors, as well as magnesium diboride superconductors.

High-temperature superconductivity (high-Tc or HTS) is superconductivity in materials with a critical temperature (the temperature below which the material behaves as a superconductor) above 77 K (−196.2 °C; −321.1 °F), the boiling point of liquid nitrogen. They are "high-temperature" only relative to previously known superconductors, which function only closer to absolute zero. The first high-temperature superconductor was discovered in 1986 by IBM researchers Georg Bednorz and K. Alex Müller.[62][63] Although the critical temperature is around 35.1 K (−238.1 °C; −396.5 °F), this material was modified by Ching-Wu Chu to make the first high-temperature superconductor with critical temperature 93 K (−180.2 °C; −292.3 °F). Bednorz and Müller were awarded the Nobel Prize in Physics in 1987 "for their important break-through in the discovery of superconductivity in ceramic materials". Most high-Tc materials are type-II superconductors.

The major advantage of high-temperature superconductors is that they can be cooled using liquid nitrogen, in contrast to previously known superconductors, which require expensive and hard-to-handle coolants, primarily liquid helium. A second advantage of high-Tc materials is they retain their superconductivity in higher magnetic fields than previous materials. This is important when constructing superconducting magnets, a primary application of high-Tc materials.

The majority of high-temperature superconductors are ceramics, rather than the previously known metallic materials. Ceramic superconductors are suitable for some practical uses but encounter manufacturing issues. For example, most ceramics are brittle, which complicates wire fabrication.

The main class of high-temperature superconductors is copper oxides combined with other metals, especially the rare-earth barium copper oxides (REBCOs) such as yttrium barium copper oxide (YBCO). The second class of high-temperature superconductors in the practical classification is the iron-based compoundsMagnesium diboride is sometimes included in high-temperature superconductors: It is relatively simple to manufacture, but it superconducts only below 39 K (−234.2 °C), which makes it unsuitable for liquid nitrogen cooling.

Applications

Superconductors are promising candidate materials for devising fundamental circuit elements of electronic, spintronic, and quantum technologies. One such example is a superconducting diode, in which supercurrent flows along one direction only, that promise dissipationless superconducting and semiconducting-superconducting hybrid technologies.

Superconducting magnets are some of the most powerful electromagnets known. They are used in MRI/NMR machines, mass spectrometers, the beam-steering magnets used in particle accelerators and plasma confining magnets in some tokamaks. They can also be used for magnetic separation, where weakly magnetic particles are extracted from a background of less or non-magnetic particles, as in the pigment industries. They can also be used in large wind turbines to overcome the restrictions imposed by high electrical currents, with an industrial grade 3.6 megawatt superconducting windmill generator having been tested successfully in Denmark.

In the 1950s and 1960s, superconductors were used to build experimental digital computers using cryotron switches. More recently, superconductors have been used to make digital circuits based on rapid single flux quantum technology and RF and microwave filters for mobile phone base stations.

Superconductors are used to build Josephson junctions which are the building blocks of SQUIDs (superconducting quantum interference devices), the most sensitive magnetometers known. SQUIDs are used in scanning SQUID microscopes and magnetoencephalography. Series of Josephson devices are used to realize the SI volt. Superconducting photon detectors can be realised in a variety of device configurations. Depending on the particular mode of operation, a superconductor–insulator–superconductor Josephson junction can be used as a photon detector or as a mixer. The large resistance change at the transition from the normal to the superconducting state is used to build thermometers in cryogenic micro-calorimeter photon detectors. The same effect is used in ultrasensitive bolometers made from superconducting materials. Superconducting nanowire single-photon detectors offer high speed, low noise single-photon detection and have been employed widely in advanced photon-counting applications.

Other early markets are arising where the relative efficiency, size and weight advantages of devices based on high-temperature superconductivity outweigh the additional costs involved. For example, in wind turbines the lower weight and volume of superconducting generators could lead to savings in construction and tower costs, offsetting the higher costs for the generator and lowering the total levelized cost of electricity (LCOE).

Promising future applications include high-performance smart grid, electric power transmission, transformers, power storage devices, compact fusion power devices, electric motors (e.g. for vehicle propulsion, as in vactrains or maglev trains), magnetic levitation devices, fault current limiters, enhancing spintronic devices with superconducting materials, and superconducting magnetic refrigeration. However, superconductivity is sensitive to moving magnetic fields, so applications that use alternating current (e.g. transformers) will be more difficult to develop than those that rely upon direct current. Compared to traditional power lines, superconducting transmission lines are more efficient and require only a fraction of the space, which would not only lead to a better environmental performance but could also improve public acceptance for expansion of the electric grid. Another attractive industrial aspect is the ability for high power transmission at lower voltages. Advancements in the efficiency of cooling systems and use of cheap coolants such as liquid nitrogen have also significantly decreased cooling costs needed for superconductivity.

Nobel Prizes

As of 2022, there have been five Nobel Prizes in Physics for superconductivity related subjects:

Chemical engineering

From Wikipedia, the free encyclopedia
Chemical engineers design, construct, and operate process plants, such as these fractionating columns.

Chemical engineering is an engineering field which deals with the study of the operation and design of chemical plants as well as methods of improving production. Chemical engineers develop economical commercial processes to convert raw materials into useful products. Chemical engineering uses principles of chemistry, physics, mathematics, biology, and economics to efficiently use, produce, design, transport and transform energy and materials. The work of chemical engineers can range from the utilization of nanotechnology and nanomaterials in the laboratory to large-scale industrial processes that convert chemicals, raw materials, living cells, microorganisms, and energy into useful forms and products. Chemical engineers are involved in many aspects of plant design and operation, including safety and hazard assessments, process design and analysis, modeling, control engineering, chemical reaction engineering, nuclear engineering, biological engineering, construction specification, and operating instructions.

Chemical engineers typically hold a degree in Chemical Engineering or Process Engineering. Practicing engineers may have professional certification and be accredited members of a professional body. Such bodies include the Institution of Chemical Engineers (IChemE) or the American Institute of Chemical Engineers (AIChE) and respective states in the U.S., which ultimately confer licensure and title of Professional Engineer. A degree in chemical engineering is directly linked with all of the other engineering disciplines, to various extents.

Etymology

George E. Davis (1850–1907) is regarded as the founding father of the discipline of chemical engineering.

A 1996 article cites James F. Donnelly for mentioning an 1839 reference to chemical engineering in relation to the production of sulfuric acid. In the same paper, however, George E. Davis, an English consultant, was credited with having coined the term. Davis also tried to found a Society of Chemical Engineering, but instead, it was named the Society of Chemical Industry (1881), with Davis as its first secretary. The History of Science in United States: An Encyclopedia puts the use of the term around 1890. "Chemical engineering", describing the use of mechanical equipment in the chemical industry, became common vocabulary in England after 1850. By 1910, the profession, "chemical engineer", was already in common use in Britain and the United States.

History

New concepts and innovations

Demonstration model of a direct-methanol fuel cell. The actual fuel cell stack is the layered cube shape in the center of the image.
Technician with equipment at the Continental Carbon Company.

In the 1940s, it became clear that unit operations alone were insufficient in developing chemical reactors. While the predominance of unit operations in chemical engineering courses in Britain and the United States continued until the 1960s, transport phenomena started to receive greater focus. Along with other novel concepts, such as process systems engineering (PSE), a "second paradigm" was defined. Transport phenomena gave an analytical approach to chemical engineering while PSE focused on its synthetic elements, such as those of a control system and process design. Developments in chemical engineering before and after World War II were mainly incited by the petrochemical industry; however, advances in other fields were made as well. Advancements in biochemical engineering in the 1940s, for example, found application in the pharmaceutical industry, and allowed for the mass production of various antibiotics, including penicillin and streptomycin. Meanwhile, progress in polymer science in the 1950s paved way for the "age of plastics".

Safety and hazard developments

Concerns regarding large-scale chemical manufacturing facilities' safety and environmental impact were also raised during this period. Silent Spring, published in 1962, alerted its readers to the harmful effects of DDT, a potent insecticide. The 1974 Flixborough disaster in the United Kingdom resulted in 28 deaths, as well as damage to a chemical plant and three nearby villages. 1984 Bhopal disaster in India resulted in at least 4,000 deaths. These incidents, along with other incidents, affected the reputation of the trade as industrial safety and environmental protection were given more focus. In response, the IChemE required safety to be part of every degree course that it accredited after 1982. By the 1970s, legislation and monitoring agencies were instituted in various countries, such as France, Germany, and the United States. In time, the systematic application of safety principles to chemical and other process plants began to be considered a specific discipline, known as process safety.

Recent progress

Advancements in computer science found applications for designing and managing plants, simplifying calculations and drawings that previously had to be done manually. Programs such as Aspen HYSYS were developed to complete multiple chemical engineering calculations. The completion of the Human Genome Project is also seen as a major development, not only advancing chemical engineering but genetic engineering and genomics as well. Chemical engineering principles were used to produce DNA sequences in large quantities.

Concepts

Plant design and construction

Chemical engineering design concerns the creation of plans, specifications, and economic analyses for pilot plants, new plants, or plant modifications. Design engineers often work in a consulting role, designing plants to meet clients' needs. Design is limited by several factors, including funding, government regulations, and safety standards. These constraints dictate a plant's choice of process, materials, and equipment.

Plant construction is coordinated by project engineers and project managers, depending on the size of the investment. A chemical engineer may do the job of project engineer full-time or part of the time, which requires additional training and job skills or act as a consultant to the project group. In the USA the education of chemical engineering graduates from the Baccalaureate programs accredited by ABET do not usually stress project engineering education, which can be obtained by specialized training, as electives, or from graduate programs. Project engineering jobs are some of the largest employers for chemical engineers.

Process design and analysis

A unit operation is a physical step in an individual chemical engineering process. Unit operations (such as crystallization, filtration, drying and evaporation) are used to prepare reactants, purifying and separating its products, recycling unspent reactants, and controlling energy transfer in reactors. On the other hand, a unit process is the chemical equivalent of a unit operation. Along with unit operations, unit processes constitute a process operation. Unit processes (such as nitration, hydrogenation, and oxidation) involve the conversion of materials by biochemical, thermochemical and other means. Chemical engineers responsible for these are called process engineers.

Process design requires the definition of equipment types and sizes as well as how they are connected and the materials of construction. Details are often printed on a Process Flow Diagram which is used to control the capacity and reliability of a new or existing chemical factory.

Education for chemical engineers in the first college degree 3 or 4 years of study stresses the principles and practices of process design. The same skills are used in existing chemical plants to evaluate the efficiency and make recommendations for improvements.

Transport phenomena

Modeling and analysis of transport phenomena is essential for many industrial applications. Transport phenomena involve fluid dynamics, heat transfer and mass transfer, which are governed mainly by momentum transfer, energy transfer and transport of chemical species, respectively. Models often involve separate considerations for macroscopic, microscopic and molecular level phenomena. Modeling of transport phenomena, therefore, requires an understanding of applied mathematics.

Applications and practice

Two computer flat screens showing a plant process management application
Chemical engineers use computers to control automated systems in plants

Chemical engineers develop economic ways of using materials and energy. Chemical engineers use chemistry and engineering to turn raw materials into usable products, such as medicine, petrochemicals, and plastics on a large-scale, industrial setting. They are also involved in waste management and research. Both applied and research facets could make extensive use of computers.

Chemical engineers may be involved in industry or university research where they are tasked with designing and performing experiments, by scaling up theoretical chemical reactions, to create better and safer methods for production, pollution control, and resource conservation. They may be involved in designing and constructing plants as a project engineer. Chemical engineers serving as project engineers use their knowledge in selecting optimal production methods and plant equipment to minimize costs and maximize safety and profitability. After plant construction, chemical engineering project managers may be involved in equipment upgrades, troubleshooting, and daily operations in either full-time or consulting roles.

Occupational outlook

According to the U.S. Bureau of Labor Statistics, the occupational outlook for chemical engineers between 2024 and 2034 was 3% growth.

Industrial fermentation

From Wikipedia, the free encyclopedia

Industrial fermentation is the intentional use of fermentation in manufacturing processes. In addition to the mass production of fermented foods and drinks, industrial fermentation has widespread applications in chemical industry. Commodity chemicals, such as acetic acid, citric acid, and ethanol are made by fermentation. Moreover, nearly all commercially produced industrial enzymes, such as lipase, invertase and rennet, are made by fermentation with genetically modified microbes. In some cases, production of biomass itself is the objective, as is the case for single-cell proteins, baker's yeast, and starter cultures for lactic acid bacteria used in cheesemaking.

In general, fermentations can be divided into four types:

  • Production of biomass (viable cellular material)
  • Production of extracellular metabolites (chemical compounds)
  • Production of intracellular components (enzymes and other proteins)
  • Transformation of substrate (in which the transformed substrate is itself the product)

These types are not necessarily disjoined from each other, but provide a framework for understanding the differences in approach. The organisms used are typically microorganisms, particularly bacteria, algae, and fungi, such as yeasts and molds, but industrial fermentation may also involve cell cultures from plants and animals, such as CHO cells and insect cells. Special considerations are required for the specific organisms used in the fermentation, such as the dissolved oxygen level, nutrient levels, and temperature. The rate of fermentation depends on the concentration of microorganisms, cells, cellular components, and enzymes as well as temperature, pH and level of oxygen for aerobic fermentation. Product recovery frequently involves the concentration of the dilute solution.

General process overview

In most industrial fermentations, the organisms or eukaryotic cells are submerged in a liquid medium; in others, such as the fermentation of cocoa beans, coffee cherries, and miso, fermentation takes place on the moist surface of the medium.

There are also industrial considerations related to the fermentation process. For instance, to avoid biological process contamination, the fermentation medium, air, and equipment are sterilized. Foam control can be achieved by either mechanical foam destruction or chemical anti-foaming agents. Several other factors must be measured and controlled such as pressure, temperature, agitator shaft power, and viscosity. An important element for industrial fermentations is scale up. This is the conversion of a laboratory procedure to an industrial process. It is well established in the field of industrial microbiology that what works well at the laboratory scale may work poorly or not at all when first attempted at large scale. It is generally not possible to take fermentation conditions that have worked in the laboratory and blindly apply them to industrial scale equipment. Although many parameters have been tested for use as scale up criteria, there is no general formula because of the variation in fermentation processes. The most important methods are the maintenance of constant power consumption per unit of broth and the maintenance of constant volumetric transfer rate.

Phases of growth

Bacterial growth curve

Fermentation begins once the growth medium is inoculated with the organism of interest. Growth of the inoculum does not occur immediately. This is the period of adaptation, called the lag phase. Following the lag phase, the rate of growth of the organism steadily increases, for a certain period—this period is the log or exponential phase.

After a phase of exponential growth, the rate of growth slows down, due to the continuously falling concentrations of nutrients and/or a continuously increasing (accumulating) concentrations of toxic substances. This phase, where the increase of the rate of growth is checked, is the deceleration phase. After the deceleration phase, growth ceases and the culture enters a stationary phase or a steady state. The biomass remains constant, except when certain accumulated chemicals in the culture chemically break down the cells in a process called chemolysis. Unless other microorganisms contaminate the culture, the chemical constitution remains unchanged. If all of the nutrients in the medium are consumed, or if the concentration of toxins is too great, the cells may become senescent and begin to die off. The total amount of biomass may not decrease, but the number of viable organisms will decrease.

Fermentation medium

The microbes or eukaryotic cells used for fermentation grow in (or on) specially designed growth medium which supplies the nutrients required by the organisms or cells. A variety of media exist, but invariably contain a carbon source, a nitrogen source, water, salts, and micronutrients. In the production of wine, the medium is grape must. In the production of bio-ethanol, the medium may consist mostly of whatever inexpensive carbon source is available.

Carbon sources are typically sugars or other carbohydrates, although in the case of substrate transformations (such as the production of vinegar) the carbon source may be an alcohol or something else altogether. For large scale fermentations, such as those used for the production of ethanol, inexpensive sources of carbohydrates, such as molasses, corn steep liquor, sugar cane juice, or sugar beet juice are used to minimize costs. More sensitive fermentations may instead use purified glucose, sucrose, glycerol or other sugars, which reduces variation and helps ensure the purity of the final product. Organisms meant to produce enzymes such as beta galactosidase, invertase or other amylases may be fed starch to select for organisms that express the enzymes in large quantity.

Fixed nitrogen sources are required for most organisms to synthesize proteins, nucleic acids and other cellular components. Depending on the enzyme capabilities of the organism, nitrogen may be provided as bulk protein, such as soy meal; as pre-digested polypeptides, such as peptone or tryptone; or as ammonia or nitrate salts. Cost is also an important factor in the choice of a nitrogen source. Phosphorus is needed for production of phospholipids in cellular membranes and for the production of nucleic acids. The amount of phosphate which must be added depends upon the composition of the broth and the needs of the organism, as well as the objective of the fermentation. For instance, some cultures will not produce secondary metabolites in the presence of phosphate.

Growth factors and trace nutrients are included in the fermentation broth for organisms incapable of producing all of the vitamins they require. Yeast extract is a common source of micronutrients and vitamins for fermentation media. Inorganic nutrients, including trace elements such as iron, zinc, copper, manganese, molybdenum, and cobalt are typically present in unrefined carbon and nitrogen sources, but may have to be added when purified carbon and nitrogen sources are used. Fermentations which produce large amounts of gas (or which require the addition of gas) will tend to form a layer of foam, since fermentation broth typically contains a variety of foam-reinforcing proteins, peptides or starches. To prevent this foam from occurring or accumulating, antifoaming agents may be added. Mineral buffering salts, such as carbonates and phosphates, may be used to stabilize pH near optimum. When metal ions are present in high concentrations, use of a chelating agent may be necessary.

Developing an optimal medium for fermentation is a key concept in efficient optimization. One-factor-at-a-time (OFAT) is the preferential choice that researchers use for designing a medium composition. This method involves changing only one factor at a time while keeping the other concentrations constant. This method can be separated into some sub groups. One is Removal Experiments. In this experiment all the components of the medium are removed one at a time and their effects on the medium are observed. Supplementation experiments involve evaluating the effects of nitrogen and carbon supplements on production. The final experiment is a replacement experiment. This involves replacing the nitrogen and carbon sources that show an enhancement effect on the intended production. Overall OFAT is a major advantage over other optimization methods because of its simplicity.

Production of biomass

Microbial cells or biomass is sometimes the intended product of fermentation. Examples include single cell protein, bakers yeast, lactobacillus, E. coli, and others. In the case of single-cell protein, algae is grown in large open ponds which allow photosynthesis to occur. If the biomass is to be used for inoculation of other fermentations, care must be taken to prevent mutations from occurring.

Production of extracellular metabolites

Metabolites can be divided into two groups: those produced during the growth phase of the organism, called primary metabolites and those produced during the stationary phase, called secondary metabolites. Some examples of primary metabolites are ethanol, citric acid, glutamic acid, lysine, vitamins and polysaccharides. Some examples of secondary metabolites are penicillin, cyclosporin A, gibberellin, and lovastatin.

Primary metabolites

Primary metabolites are compounds made during the ordinary metabolism of the organism during the growth phase. A common example is ethanol or lactic acid, produced during glycolysis. Citric acid is produced by some strains of Aspergillus niger as part of the citric acid cycle to acidify their environment and prevent competitors from taking over. Glutamate is produced by some Micrococcus species, and some Corynebacterium species produce lysine, threonine, tryptophan and other amino acids. All of these compounds are produced during the normal "business" of the cell and released into the environment. There is therefore no need to rupture the cells for product recovery.

Secondary metabolites

Secondary metabolites are compounds made in the stationary phase; penicillin, for instance, prevents the growth of bacteria which could compete with Penicillium molds for resources. Some bacteria, such as Lactobacillus species, are able to produce bacteriocins which prevent the growth of bacterial competitors as well. These compounds are of obvious value to humans wishing to prevent the growth of bacteria, either as antibiotics or as antiseptics (such as gramicidin S). Fungicides, such as griseofulvin are also produced as secondary metabolites. Typically secondary metabolites are not produced in the presence of glucose or other carbon sources which would encourage growth, and like primary metabolites are released into the surrounding medium without rupture of the cell membrane.

In the early days of the biotechnology industry, most biopharmaceutical products were made in E. coli; by 2004 more biopharmaceuticals were manufactured in eukaryotic cells, such as CHO cells, than in microbes, but used similar bioreactor systems. Insect cell culture systems came into use in the 2000s as well.

Production of intracellular components

Of primary interest among the intracellular components are microbial enzymes: catalase, amylase, protease, pectinase, cellulase, hemicellulase, lipase, lactase, streptokinase and many others. Recombinant proteins, such as insulin, hepatitis B vaccine, interferon, granulocyte colony-stimulating factor, streptokinase and others are also made this way. The largest difference between this process and the others is that the cells must be ruptured (lysed) at the end of fermentation, and the environment must be manipulated to maximize the amount of the product. Furthermore, the product (typically a protein) must be separated from all of the other cellular proteins in the lysate to be purified.

Transformation of substrate

Substrate transformation involves the transformation of a specific compound into another, such as in the case of phenylacetylcarbinol, and steroid biotransformation, or the transformation of a raw material into a finished product, in the case of food fermentations and sewage treatment.

Food fermentation

In the history of food, ancient fermented food processes, such as making bread, wine, cheese, curds, idli, dosa, among others can be dated to more than seven thousand years ago. They were developed long before humanity had any knowledge of the existence of the microorganisms involved. Some foods such as Marmite are the byproduct of the fermentation process, in this case in the production of beer.

Ethanol fuel

Fermentation is the main source of ethanol in the production of ethanol fuel. Common crops such as sugar cane, potato, cassava, and maize are fermented by yeast to produce ethanol which is further processed to become fuel.

Sewage treatment

In the process of sewage treatment, sewage is digested by enzymes secreted by bacteria. Solid organic matters are broken down into harmless, soluble substances and carbon dioxide. Liquids that result are disinfected to remove pathogens before being discharged into rivers or the sea or can be used as liquid fertilizers. Digested solids, known also as sludge, is dried and used as fertilizer. Gaseous byproducts such as methane can be utilized as biogas to fuel electrical generators. One advantage of bacterial digestion is that it reduces the bulk and odor of sewage, thus reducing space needed for dumping. The main disadvantage of bacterial digestion in sewage disposal is that it is a very slow process.

Agricultural feed

A wide variety of agroindustrial waste products can be fermented to use as food for animals, especially ruminants. Fungi have been employed to break down cellulosic wastes to increase protein content and improve in vitro digestibility.

Precision fermentation

Precision fermentation is an approach to manufacturing specific functional products which intends to minimise the production of unwanted by-products through the application of synthetic biology, particularly by generating synthetic "cell factories" with engineered genomes and metabolic pathways optimised to produce the desired compounds as efficiently as possible with the available resources. Precision fermentation of genetically modified microorganisms may be used to manufacture proteins needed for cell culture media, providing for serum-free cell culture media in the manufacturing process of cultured meat. A 2021 publication showed that photovoltaic-driven microbial protein production could use 10 times less land for an equivalent amount of protein compared to soybean cultivation. Some Food Regulatory Agencies such as the FDA do not require the labeling of precision fermented foods as GMO since they are produced by, but do not contain the genetically engineered organisms. It is unclear how regulation will be handled in EU markets, with some Startups such as Formo and Those Vegan Cowboys forming the Food Fermentation Europe (FFE) alliance together with other alt-protein startups to seek regulatory approval.

Circadian rhythm

From Wikipedia, the free encyclopedia https://en.wikipedia.org/wiki/Circadian_rhythm   Features of ...