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Monday, August 18, 2025

Thermal energy storage

From Wikipedia, the free encyclopedia
District heating accumulation tower from Theiss near Krems an der Donau in Lower Austria with a thermal capacity of 2 GWh
Thermal energy storage tower inaugurated in 2017 in Bozen-Bolzano, South Tyrol, Italy.
Construction of the salt tanks at the Solana Generating Station, which provide thermal energy storage to allow generation during night or peak demand. The 280 MW plant is designed to provide six hours of energy storage. This allows the plant to generate about 38 percent of its rated capacity over the course of a year.

Thermal energy storage (TES) is the storage of thermal energy for later reuse. Employing widely different technologies, it allows surplus thermal energy to be stored for hours, days, or months. Scale both of storage and use vary from small to large – from individual processes to district, town, or region. Usage examples are the balancing of energy demand between daytime and nighttime, storing summer heat for winter heating, or winter cold for summer cooling (Seasonal thermal energy storage). Storage media include water or ice-slush tanks, masses of native earth or bedrock accessed with heat exchangers by means of boreholes, deep aquifers contained between impermeable strata; shallow, lined pits filled with gravel and water and insulated at the top, as well as eutectic solutions and phase-change materials.

Other sources of thermal energy for storage include heat or cold produced with heat pumps from off-peak, lower cost electric power, a practice called peak shaving; heat from combined heat and power (CHP) power plants; heat produced by renewable electrical energy that exceeds grid demand and waste heat from industrial processes. Heat storage, both seasonal and short term, is considered an important means for cheaply balancing high shares of variable renewable electricity production and integration of electricity and heating sectors in energy systems almost or completely fed by renewable energy.

Categories

The kinds of thermal energy storage can be divided into three separate categories: sensible heat, latent heat, and thermo-chemical heat storage. Each of these has different advantages and disadvantages that determine their applications.

Sensible heat storage

Sensible heat storage (SHS) is the most straightforward method. It simply means the temperature of some medium is either increased or decreased. This type of storage is the most commercially available out of the three; other techniques are less developed.

The materials are generally inexpensive and safe. One of the cheapest, most commonly used options is a water tank, but materials such as molten salts or metals can be heated to higher temperatures and therefore offer a higher storage capacity. Energy can also be stored underground (UTES), either in an underground tank or in some kind of heat-transfer fluid (HTF) flowing through a system of pipes, either placed vertically in U-shapes (boreholes) or horizontally in trenches. Yet another system is known as a packed-bed (or pebble-bed) storage unit, in which some fluid, usually air, flows through a bed of loosely packed material (usually rock, pebbles or ceramic brick) to add or extract heat.

A disadvantage of SHS is its dependence on the properties of the storage medium. Storage capacities are limited by the specific heat capacity of the storage material, and the system needs to be properly designed to ensure energy extraction at a constant temperature.

Heat storage in tanks, ponds or rock caverns

A steam accumulator consists of an insulated steel pressure tank containing hot water and steam under pressure. As a heat storage device, it is used to mediate heat production by a variable or steady source from a variable demand for heat. Steam accumulators may take on a significance for energy storage in solar thermal energy projects.

Water has one of the highest thermal capacities at 4.2 kJ/(kg⋅K). Large stores, mostly hot water storage tanks, are widely used in Nordic countries to store heat for several days, to decouple heat and power production and to help meet peak demands. Some towns use insulated ponds heated by solar power as a heat source for district heating pumps. Intersessional storage in caverns has been investigated and appears to be economical and plays a significant role in heating in Finland. Energy producer Helen Oy estimates an 11.6 GWh capacity and 120 MW thermal output for its 260,000 m3 water cistern under Mustikkamaa (fully charged or discharged in 4 days at capacity), operating from 2021 to offset days of peak production/demand; while the 300,000 m3 rock caverns 50 m under sea level in Kruunuvuorenranta (near Laajasalo) were designated in 2018 to store heat in summer from warm seawater and release it in winter for district heating. In 2024, it was announced that the municipal energy supplier of Vantaa had commissioned an underground heat storage facility of over 1,100,000 cubic metres (39,000,000 cu ft) in size and 90 GWh in capacity to be built, expected to be operational in 2028.

Molten salt technology

The sensible heat of molten salt is also used for storing solar energy at a high temperature, termed molten-salt technology or molten salt energy storage (MSES). Molten salts can be employed as a thermal energy storage method to retain thermal energy. Presently, this is a commercially used technology to store the heat collected by concentrated solar power (e.g., from a solar tower or solar trough). The heat can later be converted into superheated steam to power conventional steam turbines and generate electricity at a later time. It was demonstrated in the Solar Two project from 1995 to 1999. Estimates in 2006 predicted an annual efficiency of 99%, a reference to the energy retained by storing heat before turning it into electricity, versus converting heat directly into electricity. Various eutectic mixtures of different salts are used (e.g., sodium nitrate, potassium nitrate and calcium nitrate). Experience with such systems exists in non-solar applications in the chemical and metals industries as a heat-transport fluid.

The salt melts at 131 °C (268 °F). It is kept liquid at 288 °C (550 °F) in an insulated "cold" storage tank. The liquid salt is pumped through panels in a solar collector where the focused sun heats it to 566 °C (1,051 °F). It is then sent to a hot storage tank. With proper insulation of the tank the thermal energy can be usefully stored for up to a week. When electricity is needed, the hot molten salt is pumped to a conventional steam-generator to produce superheated steam for driving a conventional turbine/generator set as used in a coal, oil, or nuclear power plant. A 100-megawatt turbine would need a tank of about 9.1 metres (30 ft) tall and 24 metres (79 ft) in diameter to drive it for four hours by this design.

A single tank with a divider plate to separate cold and hot molten salt is under development. It is more economical by achieving 100% more heat storage per unit volume over the dual tanks system as the molten-salt storage tank is costly due to its complicated construction. phase-change material (PCMs) are also used in molten-salt energy storage, while research on obtaining shape-stabilized PCMs using high porosity matrices is ongoing.

Most solar thermal power plants use this thermal energy storage concept. The Solana Generating Station in the U.S. can store 6 hours worth of generating capacity in molten salt. During the summer of 2013 the Gemasolar Thermosolar solar power-tower/molten-salt plant in Spain achieved a first by continuously producing electricity 24 hours per day for 36 days. The Cerro Dominador Solar Thermal Plant, inaugurated in June 2021, has 17.5 hours of heat storage.

Hot silicon technology

Solid or molten silicon offers much higher storage temperatures than salts with consequent greater capacity and efficiency. It is being researched as a possible more energy efficient storage technology. Silicon is able to store more than 1 MWh of energy per cubic meter at 1400 °C. An additional advantage is the relative abundance of silicon when compared to the salts used for the same purpose.

Molten aluminum

Another medium that can store thermal energy is molten (recycled) aluminum. This technology was developed by the Swedish company Azelio. The material is heated to 600 °C. When needed, the energy is transported to a Stirling engine using a heat-transfer fluid.

Heat storage using oils

Using oils as sensible heat storage materials is an effective approach for storing thermal energy, particularly in medium- to high-temperature applications. Different types of oils are used based on the temperature range and the specific requirements of the thermal energy storage system: mineral oils, synthetic oils are more recently, vegetable oils are gaining interest because they are renewable and biodegradable. Numerious criteria are used to select an oil for a particular application: high energy storage capacity and specific heat capacity, high thermal conductivity, high chemical and physical stability, low coefficient of expansion, low cost, availability, low corrosion and compatibility with compounds materials, limited environmental issues, etc. Regarding the selection of a low-cost or cost-effective thermal oil, it is important to consider not only the acquisition or purchase cost, but also the operating and replacement costs or even final disposal costs. An oil that is initially more expensive may prove to be more cost-effective in the long run if it offers higher thermal stability, thereby reducing the frequency of replacement.

Heat storage in hot rocks or concrete

Rock, sand and concrete has a heat capacity about one third of water's. On the other hand, concrete can be heated to much higher temperatures (1200 °C) by for example electrical heating and therefore has a much higher overall volumetric capacity. Thus in the example below, an insulated cube of about 2.8 m3 would appear to provide sufficient storage for a single house to meet 50% of heating demand. This could, in principle, be used to store surplus wind or solar heat due to the ability of electrical heating to reach high temperatures. At the neighborhood level, the Wiggenhausen-Süd solar development at Friedrichshafen in southern Germany has received international attention. This features a 12,000 m3 (420,000 cu ft) reinforced concrete thermal store linked to 4,300 m2 (46,000 sq ft) of solar collectors, which will supply the 570 houses with around 50% of their heating and hot water. Siemens-Gamesa built a 130 MWh thermal storage near Hamburg with 750 °C in basalt and 1.5 MW electric output. A similar system was scheduled for Sorø, Denmark, with 41–58% of the stored 18 MWh heat returned for the town's district heating, and 30–41% returned as electricity, but not retained.

“Brick toaster” is a recently (August 2022) announced innovative heat reservoir operating at up to 1,500 °C (2,732 °F) that its maker, Titan Cement/Rondo claims should be able cut global CO
2
output by 15% over 15 years.

Research into using sintered bauxite proppants as the thermal store, heating them up to 1000 °C. This material was tested against plasma-sprayed alumina and mullite, alumina fiber reinforced/alumina matrix and mullite fiber reinforced/mullite ceramic matrix composites. These four materials were considered because of their usefulness as solar receivers, transport tubes and storage tanks.

Latent heat storage

Because latent heat storage (LHS) is associated with a phase transition, the general term for the associated media is Phase-Change Material (PCM). During these transitions, heat can be added or extracted without affecting the material's temperature, giving it an advantage over SHS-technologies. Storage capacities are often higher as well.

There are a multitude of PCMs available, including but not limited to salts, polymers, gels, paraffin waxes, metal alloys and semiconductor-metal alloys, each with different properties. This allows for a more target-oriented system design. As the process is isothermal at the PCM's melting point, the material can be picked to have the desired temperature range. Desirable qualities include high latent heat and thermal conductivity. Furthermore, the storage unit can be more compact if volume changes during the phase transition are small.

PCMs are further subdivided into organic, inorganic and eutectic materials. Compared to organic PCMs, inorganic materials are less flammable, cheaper and more widely available. They also have higher storage capacity and thermal conductivity. Organic PCMs, on the other hand, are less corrosive and not as prone to phase-separation. Eutectic materials, as they are mixtures, are more easily adjusted to obtain specific properties, but have low latent and specific heat capacities.

Another important factor in LHS is the encapsulation of the PCM. Some materials are more prone to erosion and leakage than others. The system must be carefully designed in order to avoid unnecessary loss of heat.

Miscibility gap alloy technology

Miscibility gap alloys rely on the phase change of a metallic material (see: latent heat) to store thermal energy.

Rather than pumping the liquid metal between tanks as in a molten-salt system, the metal is encapsulated in another metallic material that it cannot alloy with (immiscible). Depending on the two materials selected (the phase changing material and the encapsulating material) storage densities can be between 0.2 and 2 MJ/L.

A working fluid, typically water or steam, is used to transfer the heat into and out of the system. Thermal conductivity of miscibility gap alloys is often higher (up to 400 W/(m⋅K)) than competing technologies which means quicker "charge" and "discharge" of the thermal storage is possible. The technology has not yet been implemented on a large scale.

Ice-based technology

Several applications are being developed where ice is produced during off-peak periods and used for cooling at a later time. For example, air conditioning can be provided more economically by using low-cost electricity at night to freeze water into ice, then using the cooling capacity of ice in the afternoon to reduce the electricity needed to handle air conditioning demands. Thermal energy storage using ice makes use of the large heat of fusion of water. Historically, ice was transported from mountains to cities for use as a coolant. One metric ton of water (= one cubic meter) can store 334 million joules (MJ) or 317,000 BTUs (93 kWh). A relatively small storage facility can hold enough ice to cool a large building for a day or a week.

In addition to using ice in direct cooling applications, it is also being used in heat pump-based heating systems. In these applications, the phase change energy provides a very significant layer of thermal capacity that is near the bottom range of temperature that water source heat pumps can operate in. This allows the system to ride out the heaviest heating load conditions and extends the timeframe by which the source energy elements can contribute heat back into the system.

Cryogenic energy storage

Cryogenic energy storage uses liquification of air or nitrogen as an energy store.

A pilot cryogenic energy system that uses liquid air as the energy store, and low-grade waste heat to drive the thermal re-expansion of the air, operated at a power station in Slough, UK in 2010.

Thermo-chemical heat storage

Thermo-chemical heat storage (TCS) involves some kind of reversible exotherm/endotherm chemical reaction with thermo-chemical materials (TCM) . Depending on the reactants, this method can allow for an even higher storage capacity than LHS.

In one type of TCS, heat is applied to decompose certain molecules. The reaction products are then separated, and mixed again when required, resulting in a release of energy. Some examples are the decomposition of potassium oxide (over a range of 300–800 °C, with a heat decomposition of 2.1 MJ/kg), lead oxide (300–350 °C, 0.26 MJ/kg) and calcium hydroxide (above 450 °C, where the reaction rates can be increased by adding zinc or aluminum). The photochemical decomposition of nitrosyl chloride can also be used and, since it needs photons to occur, works especially well when paired with solar energy.

Adsorption (or Sorption) solar heating and storage

Adsorption processes also fall into this category. It can be used to not only store thermal energy, but also control air humidity. Zeolites (microporous crystalline alumina-silicates) and silica gels are well suited for this purpose. In hot, humid environments, this technology is often used in combination with lithium chloride to cool water.

The low cost ($200/ton) and high cycle rate (2,000×) of synthetic zeolites such as Linde 13X with water adsorbate has garnered much academic and commercial interest recently for use for thermal energy storage (TES), specifically of low-grade solar and waste heat. Several pilot projects have been funded in the EU from 2000 to the present (2020). The basic concept is to store solar thermal energy as chemical latent energy in the zeolite. Typically, hot dry air from flat plate solar collectors is made to flow through a bed of zeolite such that any water adsorbate present is driven off. Storage can be diurnal, weekly, monthly, or even seasonal depending on the volume of the zeolite and the area of the solar thermal panels. When heat is called for during the night, or sunless hours, or winter, humidified air flows through the zeolite. As the humidity is adsorbed by the zeolite, heat is released to the air and subsequently to the building space. This form of TES, with specific use of zeolites, was first taught by Guerra in 1978. Advantages over molten salts and other high temperature TES include that (1) the temperature required is only the stagnation temperature typical of a solar flat plate thermal collector, and (2) as long as the zeolite is kept dry, the energy is stored indefinitely. Because of the low temperature, and because the energy is stored as latent heat of adsorption, thus eliminating the insulation requirements of a molten salt storage system, costs are significantly lower.

Salt hydrate technology

One example of an experimental storage system based on chemical reaction energy is the salt hydrate technology. The system uses the reaction energy created when salts are hydrated or dehydrated. It works by storing heat in a container containing 50% sodium hydroxide (NaOH) solution. Heat (e.g. from using a solar collector) is stored by evaporating the water in an endothermic reaction. When water is added again, heat is released in an exothermic reaction at 50 °C (120 °F). Current systems operate at 60% efficiency. The system is especially advantageous for seasonal thermal energy storage, because the dried salt can be stored at room temperature for prolonged times, without energy loss. The containers with the dehydrated salt can even be transported to a different location. The system has a higher energy density than heat stored in water and the capacity of the system can be designed to store energy from a few months to years.

In 2013 the Dutch technology developer TNO presented the results of the MERITS project to store heat in a salt container. The heat, which can be derived from a solar collector on a rooftop, expels the water contained in the salt. When the water is added again, the heat is released, with almost no energy losses. A container with a few cubic meters of salt could store enough of this thermochemical energy to heat a house throughout the winter. In a temperate climate like that of the Netherlands, an average low-energy household requires about 6.7 GJ/winter. To store this energy in water (at a temperature difference of 70 °C), 23 m3 insulated water storage would be needed, exceeding the storage abilities of most households. Using salt hydrate technology with a storage density of about 1 GJ/m3, 4–8 m3 could be sufficient.

As of 2016, researchers in several countries are conducting experiments to determine the best type of salt, or salt mixture. Low pressure within the container seems favorable for the energy transport. Especially promising are organic salts, so called ionic liquids. Compared to lithium halide-based sorbents they are less problematic in terms of limited global resources and compared to most other halides and sodium hydroxide (NaOH) they are less corrosive and not negatively affected by CO2 contaminations.

However, a recent meta-analysis  on studies of thermochemical heat storage suggests that salt hydrates offer very low potential for thermochemical heat storage, that absorption processes have prohibitive performance for long-term heat storage, and that thermochemical storage may not be suitable for long-term solar heat storage in buildings.

Molecular bonds

Storing energy in molecular bonds is being investigated. Energy densities equivalent to lithium-ion batteries have been achieved. This has been done by a DSPEC (dys-sensitized photoelectrosythesis cell). This is a cell that can store energy that has been acquired by solar panels during the day for night-time (or even later) use. It is designed by taking an indication from, well known, natural photosynthesis.

The DSPEC generates hydrogen fuel by making use of the acquired solar energy to split water molecules into its elements. As the result of this split, the hydrogen is isolated and the oxygen is released into the air. This sounds easier than it actually is. Four electrons of the water molecules need to be separated and transported elsewhere. Another difficult part is the process of merging the two separate hydrogen molecules.

The DSPEC consists of two components: a molecule and a nanoparticle. The molecule is called a chromophore-catalyst assembly which absorbs sunlight and kick starts the catalyst. This catalyst separates the electrons and the water molecules. The nanoparticles are assembled into a thin layer and a single nanoparticle has many chromophore-catalyst on it. The function of this thin layer of nanoparticles is to transfer away the electrons which are separated from the water. This thin layer of nanoparticles is coated by a layer of titanium dioxide. With this coating, the electrons that come free can be transferred more quickly so that hydrogen could be made. This coating is, again, coated with a protective coating that strengthens the connection between the chromophore-catalyst and the nanoparticle.

Using this method, the solar energy acquired from the solar panels is converted into fuel (hydrogen) without releasing the so-called greenhouse gasses. This fuel can be stored into a fuel cell and, at a later time, used to generate electricity.

Molecular Solar Thermal System (MOST)

Another promising way to store solar energy for electricity and heat production is a so-called molecular solar thermal system (MOST). With this approach a molecule is converted by photoisomerization into a higher-energy isomer. Photoisomerization is a process in which one (cis trans) isomer is converted into another by light (solar energy). This isomer is capable of storing the solar energy until the energy is released by a heat trigger or catalyst (then, the isomer is converted into its original isomer). A promising candidate for such a MOST is Norbornadiene (NBD). This is because there is a high energy difference between the NBD and the quadricyclane (QC) photoisomer. This energy difference is approximately 96 kJ/mol. It is also known that for such systems, the donor-acceptor substitutions provide an effective means for red shifting the longest-wavelength absorption. This improves the solar spectrum match.

A crucial challenge for a useful MOST system is to acquire a satisfactory high energy storage density (if possible, higher than 300 kJ/kg). Another challenge of a MOST system is that light can be harvested in the visible region. The functionalization of the NBD with the donor and acceptor units is used to adjust this absorption maxima. However, this positive effect on the solar absorption is compensated by a higher molecular weight. This implies a lower energy density. This positive effect on the solar absorption has another downside. Namely, that the energy storage time is lowered when the absorption is redshifted. A possible solution to overcome this anti-correlation between the energy density and the red shifting is to couple one chromophore unit to several photo switches. In this case, it is advantageous to form so called dimers or trimers. The NBD share a common donor and/or acceptor.

Kasper Moth-Poulsen and his team tried to engineer the stability of the high energy photo isomer by having two electronically coupled photo switches with separate barriers for thermal conversion. By doing so, a blue shift occurred after the first isomerization (NBD-NBD to QC-NBD). This led to a higher energy of isomerization of the second switching event (QC-NBD to QC-QC). Another advantage of this system, by sharing a donor, is that the molecular weight per norbornadiene unit is reduced. This leads to an increase of the energy density.

Eventually, this system could reach a quantum yield of photoconversion up 94% per NBD unit. A quantum yield is a measure of the efficiency of photon emission. With this system the measured energy densities reached up to 559 kJ/kg (exceeding the target of 300 kJ/kg). So, the potential of the molecular photo switches is enormous—not only for solar thermal energy storage but for other applications as well.

In 2022, researchers reported combining the MOST with a chip-sized thermoelectric generator to generate electricity from it. The system can reportedly store solar energy for up to 18 years and may be an option for renewable energy storage.

Thermal battery

A thermal energy battery is a physical structure used for the purpose of storing and releasing thermal energy. Such a thermal battery (a.k.a. TBat) allows energy available at one time to be temporarily stored and then released at another time. The basic principles involved in a thermal battery occur at the atomic level of matter, with energy being added to or taken from either a solid mass or a liquid volume which causes the substance's temperature to change. Some thermal batteries also involve causing a substance to transition thermally through a phase transition which causes even more energy to be stored and released due to the delta enthalpy of fusion or delta enthalpy of vaporization.

Thermal batteries are very common, and include such familiar items as a hot water bottle. Early examples of thermal batteries include stone and mud cook stoves, rocks placed in fires, and kilns. While stoves and kilns are ovens, they are also thermal storage systems that depend on heat being retained for an extended period of time. Thermal energy storage systems can also be installed in domestic situations with heat batteries and thermal stores being amongst the most common types of energy storage systems installed at homes in the UK.

Types of thermal batteries

Thermal batteries generally fall into 4 categories with different forms and applications, although fundamentally all are for the storage and retrieval of thermal energy. They also differ in method and density of heat storage.

Phase change thermal battery

Phase change materials used for thermal storage are capable of storing and releasing significant thermal capacity at the temperature that they change phase. These materials are chosen based on specific applications because there is a wide range of temperatures that may be useful in different applications and a wide range of materials that change phase at different temperatures. These materials include salts and waxes that are specifically engineered for the applications they serve. In addition to manufactured materials, water is a phase change material. The latent heat of water is 334 joules/gram. The phase change of water occurs at 0 °C (32 °F).

Some applications use the thermal capacity of water or ice as cold storage; others use it as heat storage. It can serve either application; ice can be melted to store heat then refrozen to warm an environment. The advantage of using a phase change in this way is that a given mass of material can absorb a large quantity of energy without its temperature changing. Hence a thermal battery that uses a phase change can be made lighter, or more energy can be put into it without raising the internal temperature unacceptably.

Encapsulated thermal battery

An encapsulated thermal battery is physically similar to a phase change thermal battery in that it is a confined amount of physical material which is thermally heated or cooled to store or extract energy. However, in a non-phase change encapsulated thermal battery, the temperature of the substance is changed without inducing a phase change. Since a phase change is not needed many more materials are available for use in an encapsulated thermal battery. One of the key properties of an encapsulated thermal battery is its volumetric heat capacity (VHC), also termed volume-specific heat capacity. Several substances are used for these thermal batteries, for example water, concrete, and wet or dry sand.

An example of an encapsulated thermal battery is a residential water heater with a storage tank. This thermal battery is usually slowly charged over a period of about 30–60 minutes for rapid use when needed (e.g., 10–15 minutes). Many utilities, understanding the "thermal battery" nature of water heaters, have begun using them to absorb excess renewable energy power when available for later use by the homeowner. According to the above-cited article, "net savings to the electricity system as a whole could be $200 per year per heater — some of which may be passed on to its owner".

A district heating storage using sand or stone operates in Pornainen in Finland, where a 1 MW / 100 MWh heat storage (using 2,000 tons of soapstone waste) is charged by surplus electricity, and can serve the area's heating demand for a week. It follows research with a prototype 0.1 MW / 8 MWh sand battery that was built in 2022 to store renewable solar and wind power as heat, for later use as district heating, and possible later power generation. In Canada, single building thermal storage also stores renewable solar and wind power as heat, for later use as space or water heating for the building in which it's installed. It differs from the system in Finland by being compact, using low pressure pumped fluids, and can only heat one building rather than several. It can take in waste heat from alternate sources such as computer server rooms or compost heaps and store it for later distribution.

Ground heat exchange thermal battery

Thermal battery
Component typeEnergy
Working principleThermodynamics
InventorHeat pumps, as used by the GHEX depicted above, were invented in the 1940s by Robert C. Webber.
First producedHeat pumps were first produced in the 1970s.

A ground heat exchanger (GHEX) is an area of the earth that is utilized as a seasonal/annual cycle thermal battery. These thermal batteries are areas of the earth into which pipes have been placed in order to transfer thermal energy. Energy is added to the GHEX by running a higher temperature fluid through the pipes and thus raising the temperature of the local earth. Energy can also be taken from the GHEX by running a lower-temperature fluid through those same pipes.

GHEX are usually implemented in two forms. The picture above depicts what is known as a "horizontal" GHEX where trenching is used to place an amount of pipe in a closed loop in the ground. They are also formed by drilling boreholes into the ground, either vertically or horizontally, and then the pipes are inserted in the form of a closed-loop with a "u-bend" fitting on the far end of the loop.

Heat energy can be added to or removed from a GHEX at any point in time. However, they are most often used as a Seasonal thermal energy storage operating on an annual cycle where energy is extracted from a building during the summer season to cool a building and added to the GHEX. Then that same energy is later extracted from the GHEX in the winter season to heat the building. This annual cycle of energy addition and subtraction is highly predictable based on energy modelling of the building served. A thermal battery used in this mode is a renewable energy source as the energy extracted in the winter will be restored to the GHEX the next summer in a continually repeating cycle. This type is solar powered because it is the heat from the sun in the summer that is removed from a building and stored in the ground for use in the next winter season for heating. There are two main methods of Thermal Response Testing that are used to characterize the thermal conductivity and Thermal Capacity/Diffusivity of GHEX Thermal Batteries—Log-Time 1-Dimensional Curve Fit and newly released Advanced Thermal Response Testing.

A good example of the Annual Cycle nature of a GHEX Thermal Battery can be seen in the ASHRAE Building study. As seen there in the 'Ground Loop and Ambient Air temperatures by date' graphic (Figure 2–7), one can easily see the annual cycle sinusoidal shape of the ground temperature as heat is seasonally extracted from the ground in winter and rejected to the ground in summer, creating a ground "thermal charge" in one season that is not uncharged and driven the other direction from neutral until a later season. Other more advanced examples of Ground-based Thermal Batteries utilizing intentional well-bore thermal patterns are currently in research and early use.

Molten-salt batteries

In the defense industry primary molten-salt batteries are termed "thermal batteries". They are non-rechargeable electrical batteries using a low-melting eutectic mixture of ionic metal salts (sodium, potassium and lithium chlorides, bromides, etc.) as the electrolyte, manufactured with the salts in solid form. As long as the salts remain solid, the battery has a long shelf life of up to 50 years. Once activated (usually by a pyrotechnic heat source) and the electrolyte melts, it is very reliable with a high energy and power density. They are extensively used for military applications such as small to large guided missiles, and nuclear weapons.

Other thermal batteries

There are other items that have historically been termed "thermal batteries", such as energy-storage heat packs that skiers use for keeping hands and feet warm (see hand warmer). These contain iron powder moist with oxygen-free salt water which rapidly corrodes over a period of hours, releasing heat, when exposed to air. Instant cold packs absorb heat by a non-chemical phase-change such as by absorbing the endothermic heat of solution of certain compounds.

The one common principle of these other thermal batteries is that the reaction involved is not reversible. Thus, these batteries are not used for storing and retrieving heat energy.

Electric thermal storage

Storage heaters are commonplace in European homes with time-of-use metering (traditionally using cheaper electricity at nighttime). They consist of high-density ceramic bricks or feolite blocks heated to a high temperature with electricity and may or may not have good insulation and controls to release heat over a number of hours. Some advice not to use them in areas with young children or where there is an increased risk of fires due to poor housekeeping, both due to the high temperatures involved.

With the rise of wind and solar power (and other renewable energies) providing an ever increasing share of energy input into the electricity grids in some countries, the use of larger scale electric energy storage is being explored by several commercial companies. Ideally, the utilisation of surplus renewable energy is transformed into high temperature high grade heat in highly insulated heat stores, for release later when needed. An emerging technology is the use of vacuum super insulated (VSI) heat stores. The use of electricity to generate heat, and not say direct heat from solar thermal collectors, means that very high temperatures can be realised, potentially allowing for inter seasonal heat transfer—storing high grade heat in summer from surplus photovoltaics generation into heat stored for the following winter with relatively minimal standing losses.

Solar energy storage

Solar energy is an application of thermal energy storage. Most practical solar thermal storage systems provide storage from a few hours to a day's worth of energy. However, a growing number of facilities use seasonal thermal energy storage (STES), enabling solar energy to be stored in summer to heat space during winter. In 2017 Drake Landing Solar Community in Alberta, Canada, achieved a year-round 97% solar heating fraction, a world record made possible by incorporating STES.

The combined use of latent heat and sensible heat are possible with high temperature solar thermal input. Various eutectic metal mixtures, such as aluminum and silicon (AlSi
12
) offer a high melting point suited to efficient steam generation, while high alumina cement-based materials offer good storage capabilities.

Pumped-heat electricity storage

In pumped-heat electricity storage (PHES), a reversible heat-pump system is used to store energy as a temperature difference between two heat stores.

Isentropic

Isentropic systems involve two insulated containers filled, for example, with crushed rock or gravel: a hot vessel storing thermal energy at high temperature/pressure, and a cold vessel storing thermal energy at low temperature/pressure. The vessels are connected at top and bottom by pipes and the whole system is filled with an inert gas such as argon.

While charging, the system can use off-peak electricity to work as a heat pump. One prototype used argon at ambient temperature and pressure from the top of the cold store is compressed adiabatically, to a pressure of, for example, 12 bar, heating it to around 500 °C (900 °F). The compressed gas is transferred to the top of the hot vessel where it percolates down through the gravel, transferring heat to the rock and cooling to ambient temperature. The cooled, but still pressurized, gas emerging at the bottom of the vessel is then adiabatically expanded to 1 bar, which lowers its temperature to −150 °C. The cold gas is then passed up through the cold vessel where it cools the rock while warming to its initial condition.

The energy is recovered as electricity by reversing the cycle. The hot gas from the hot vessel is expanded to drive a generator and then supplied to the cold store. The cooled gas retrieved from the bottom of the cold store is compressed which heats the gas to ambient temperature. The gas is then transferred to the bottom of the hot vessel to be reheated.

The compression and expansion processes are provided by a specially designed reciprocating machine using sliding valves. Surplus heat generated by inefficiencies in the process is shed to the environment through heat exchangers during the discharging cycle.

The developer claimed that a round trip efficiency of 72–80% was achievable. This compares to >80% achievable with pumped hydro energy storage.

Another proposed system uses turbomachinery and is capable of operating at much higher power levels. Use of phase change material as heat storage material could enhance performance.

Octet rule

From Wikipedia, the free encyclopedia
The bonding in carbon dioxide (CO2): all atoms are surrounded by 8 electrons, fulfilling the octet rule.

The octet rule is a chemical rule of thumb that reflects the theory that main-group elements tend to bond in such a way that each atom has eight electrons in its valence shell, giving it the same electronic configuration as a noble gas. The rule is especially applicable to carbon, nitrogen, oxygen, and the halogens, although more generally the rule is applicable for the s-block and p-block of the periodic table. Other rules exist for other elements, such as the duplet rule for hydrogen and helium, and the 18-electron rule for transition metals.

The valence electrons in molecules like carbon dioxide (CO2) can be visualized using a Lewis electron dot diagram. In covalent bonds, electrons shared between two atoms are counted toward the octet of both atoms. In carbon dioxide each oxygen shares four electrons with the central carbon, two (shown in red) from the oxygen itself and two (shown in black) from the carbon. All four of these electrons are counted in both the carbon octet and the oxygen octet, so that both atoms are considered to obey the octet rule.

Example: sodium chloride (NaCl)

The octet rule is simplest in the case of ionic bonding between two atoms, one a metal of low electronegativity and the other a nonmetal of high electronegativity. For example, sodium metal and chlorine gas combine to form sodium chloride, a crystal lattice composed of alternating sodium and chlorine nuclei. Electron density inside this lattice forms clumps at the atomic scale, as follows.

An isolated chlorine atom (Cl) has two and eight electrons in its first and second electron shells, located near the nucleus. However, it has only seven electrons in the third and outermost electron shell. One additional electron would completely fill the outer electron shell with eight electrons, a situation the octet rule commends. Indeed, adding an electron to the produce the chloride ion (Cl) releases 3.62 eV of energy. Conversely, another surplus electron cannot fit in the same shell, instead beginning the fourth electron shell around the nucleus. Thus the octet rule proscribes formation of a hypothetical Cl2− ion, and indeed the latter has only been observed as a plasma under extreme conditions.

A sodium atom (Na) has a single electron in its outermost electron shell, the first and second shells again being full with two and eight electrons respectively. The octet rule favors removal of this outermost electron to form the Na+ ion, which has the exact same electron configuration as Cl. Indeed, sodium is observed to transfer one electron to chlorine during the formation of sodium chloride, such that the resulting lattice is best considered as a periodic array of Na+ and Cl ions.

To remove the outermost Na electron and return to an "octet-approved" state requires a small amount of energy: 5.14 eV. This energy is provided from the 3.62 eV released during chloride formation, and the electrostatic attraction between positively-charged Na+ and negatively-charged Cl ions, which releases a 8.12 eV lattice energy. By contrast, any further electrons removed from Na would reside in the deeper second electron shell, and produce an octet-violating Na2+ ion. Consequently, the second ionization energy required for the next removal is much larger – 47.28 eV – and the corresponding ion is only observed under extreme conditions.

History

Newlands' law of octaves

In 1864, the English chemist John Newlands classified the sixty-two known elements into eight groups, based on their physical properties.

In the late 19th century, it was known that coordination compounds (formerly called "molecular compounds") were formed by the combination of atoms or molecules in such a manner that the valencies of the atoms involved apparently became satisfied. In 1893, Alfred Werner showed that the number of atoms or groups associated with a central atom (the "coordination number") is often 4 or 6; other coordination numbers up to a maximum of 8 were known, but less frequent. In 1904, Richard Abegg was one of the first to extend the concept of coordination number to a concept of valence in which he distinguished atoms as electron donors or acceptors, leading to positive and negative valence states that greatly resemble the modern concept of oxidation states. Abegg noted that the difference between the maximum positive and negative valences of an element under his model is frequently eight. In 1916, Gilbert N. Lewis referred to this insight as Abegg's rule and used it to help formulate his cubical atom model and the "rule of eight", which began to distinguish between valence and valence electrons. In 1919, Irving Langmuir refined these concepts further and renamed them the "cubical octet atom" and "octet theory". The "octet theory" evolved into what is now known as the "octet rule".

Walther Kossel and Gilbert N. Lewis saw that noble gases did not have the tendency of taking part in chemical reactions under ordinary conditions. On the basis of this observation, they concluded that atoms of noble gases are stable and on the basis of this conclusion they proposed a theory of valency known as "electronic theory of valency" in 1916:

During the formation of a chemical bond, atoms combine together by gaining, losing or sharing electrons in such a way that they acquire nearest noble gas configuration.

Explanation in quantum theory

The quantum theory of the atom explains the eight electrons as a closed shell with an s2p6 electron configuration. A closed-shell configuration is one in which low-lying energy levels are full and higher energy levels are empty. For example, the neon atom ground state has a full n = 2 shell (2s22p6) and an empty n = 3 shell. According to the octet rule, the atoms immediately before and after neon in the periodic table (i.e. C, N, O, F, Na, Mg and Al), tend to attain a similar configuration by gaining, losing, or sharing electrons.

The argon atom has an analogous 3s23p6 configuration. There is also an empty 3d level, but it is at considerably higher energy than 3s and 3p (unlike in the hydrogen atom), so that 3s23p6 is still considered a closed shell for chemical purposes. The atoms immediately before and after argon tend to attain this configuration in compounds. There are, however, some hypervalent molecules in which the 3d level may play a part in the bonding, although this is controversial (see below).

For helium there is no 1p level according to the quantum theory, so that 1s2 is a closed shell with no p electrons. The atoms before and after helium (H and Li) follow a duet rule and tend to have the same 1s2 configuration as helium.

Exceptions

Many reactive intermediates do not obey the octet rule. Most are unstable, although some can be isolated.

Typically, octet rule violations occur in either low-dimensional coordination geometries or in radical species. Although hypervalent molecules are commonly taught to violate the octet rule, ab initio calculations show that almost all known examples obey the octet rule. The compounds form many fractional bonds through resonance (see § Hypervalent molecules below).

Low-dimensional geometries

In the trigonal planar coordination geometry, one p orbital points out of the bonding plane, and can only overlap with nearby atomic orbitals in a π bond. If that p orbital would be empty in an isolated atom, it may be filled through an intramolecular dative bond, as with aminoboranes. However, in some cases (e.g. boron trichloride and various boranes, triphenylmethanium), no nearby filled orbital can profitably overlap with the empty p orbital. In such cases, the orbital remains empty, and the compound obeys a "sextet rule". Likewise, linear compounds, such as dimethylzinc, have two p orbitals perpendicular to the bonding axis, and may obey a "quartet rule". In either case, the empty unshielded orbitals tend to attract adducts.

Radicals

Radicals satisfy the octet rule in one spin orientation, with four spin-up electrons in the valence shell, and almost satisfy it in the opposite spin orientation. Thus, for example, the methyl radical (CH3), which has an unpaired electron in a non-bonding orbital on the carbon atom and no electron of opposite spin in the same orbital. Another example is the radical chlorine monoxide (ClO) which is involved in ozone depletion.

Stable radicals tend to adopt states in which the unpaired electron can delocalize through resonance. In such cases, the octet rule can be restored through the formalism of a 1- or 3-electron bond.

Species such as carbenes can be interpreted two different ways, depending on their spin state. Triplet carbenes are best thought of as two radicals localized on the same atom, and obey the octet rule in those radicals' shared spin-up orientation. Singlet carbenes tend to adopt a planar configuration, and are best thought of as obeying the planar sextet rule.

Hypervalent molecules

Main-group elements in the third and later rows of the periodic table can form hypercoordinate or hypervalent molecules in which the central main-group atom is bonded to more than four other atoms, such as phosphorus pentafluoride, PF5, and sulfur hexafluoride, SF6. For example, in PF5, if it is supposed that there are five true covalent bonds in which five distinct electron pairs are shared, then the phosphorus would be surrounded by 10 valence electrons in violation of the octet rule. In the early days of quantum mechanics, Pauling proposed that third-row atoms can form five bonds by using one s, three p and one d orbitals, or six bonds by using one s, three p and two d orbitals. To form five bonds, the one s, three p and one d orbitals combine to form five sp3d hybrid orbitals which each share an electron pair with a halogen atom, for a total of 10 shared electrons, two more than the octet rule predicts. Similarly to form six bonds, the six sp3d2 hybrid orbitals form six bonds with 12 shared electrons. In this model the availability of empty d orbitals is used to explain the fact that third-row atoms such as phosphorus and sulfur can form more than four covalent bonds, whereas second-row atoms such as nitrogen and oxygen are strictly limited by the octet rule.

5 resonance structures of phosphorus pentafluoride

However other models describe the bonding using only s and p orbitals in agreement with the octet rule. A valence bond description of PF5 uses resonance between different PF4+ F structures, so that each F is bonded by a covalent bond in four structures and an ionic bond in one structure. Each resonance structure has eight valence electrons on P. A molecular orbital theory description considers the highest occupied molecular orbital to be a non-bonding orbital localized on the five fluorine atoms, in addition to four occupied bonding orbitals, so again there are only eight valence electrons on the phosphorus. The validity of the octet rule for hypervalent molecules is further supported by ab initio molecular orbital calculations, which show that the contribution of d functions to the bonding orbitals is small.

Nevertheless, for historical reasons, structures implying more than eight electrons around elements like P, S, Se, or I are still common in textbooks and research articles. In spite of the unimportance of d shell expansion in chemical bonding, this practice allows structures to be shown without using a large number of formal charges or using partial bonds and is recommended by the IUPAC as a convenient formalism in preference to depictions that better reflect the bonding. On the other hand, showing more than eight electrons around Be, B, C, N, O, or F (or more than two around H, He, or Li) is considered an error by most authorities. In particular, instead of pentavalent N, tetravalent N+ is written (e. g. not H−O−N(=O)=O but H−O−N+(=O)−O).

Other rules

The octet rule is only applicable to main-group elements. Other elements follow other electron counting rules as their valence electron configurations are different from main-group elements. These other rules are shown below:

Element type First shell p-block
(Main group)
d-block
(Transition metal)
Electron counting rules Duet/Duplet rule Octet rule 18-electron rule
Full valence configuration s2 s2p6 d10s2p6
  • The duet rule or duplet rule of the first shell applies to H, He and Li—the noble gas helium has two electrons in its outer shell, which is very stable. (Since there is no 1p subshell, 1s is followed immediately by 2s, and thus shell 1 can only have at most 2 valence electrons). Hydrogen only needs one additional electron to attain this stable configuration, while lithium needs to lose one.
  • For transition metals, molecules tend to obey the 18-electron rule which corresponds to the utilization of valence d, s and p orbitals to form bonding and non-bonding orbitals. However, unlike the octet rule for main-group elements, transition metals do not strictly obey the 18-electron rule and the valence electron count can vary between 12 and 18.

Endocrine system

From Wikipedia, the free encyclopedia
 
Endocrine system
Main glands of the human endocrine system

The endocrine system is a messenger system in an organism comprising feedback loops of hormones that are released by internal glands directly into the circulatory system and that target and regulate distant organs. In vertebrates, the hypothalamus is the neural control center for all endocrine systems.

In humans, the major endocrine glands are the thyroid, parathyroid, pituitary, pineal, and adrenal glands, and the (male) testis and (female) ovaries. The hypothalamus, pancreas, and thymus also function as endocrine glands, among other functions. (The hypothalamus and pituitary glands are organs of the neuroendocrine system. One of the most important functions of the hypothalamus—it is located in the brain adjacent to the pituitary gland—is to link the endocrine system to the nervous system via the pituitary gland.) Other organs, such as the kidneys, also have roles within the endocrine system by secreting certain hormones. The study of the endocrine system and its disorders is known as endocrinology. The thyroid secretes thyroxine, the pituitary secretes growth hormone, the pineal secretes melatonin, the testis secretes testosterone, and the ovaries secrete estrogen and progesterone.

Glands that signal each other in sequence are often referred to as an axis, such as the hypothalamic–pituitary–adrenal axis. In addition to the specialized endocrine organs mentioned above, many other organs that are part of other body systems have secondary endocrine functions, including bone, kidneys, liver, heart and gonads. For example, the kidney secretes the endocrine hormone erythropoietin. Hormones can be amino acid complexes, steroids, eicosanoids, leukotrienes, or prostaglandins.

The endocrine system is contrasted both to exocrine glands, which secrete hormones to the outside of the body, and to the system known as paracrine signalling between cells over a relatively short distance. Endocrine glands have no ducts, are vascular, and commonly have intracellular vacuoles or granules that store their hormones. In contrast, exocrine glands, such as salivary glands, mammary glands, and submucosal glands within the gastrointestinal tract, tend to be much less vascular and have ducts or a hollow lumen. Endocrinology is a branch of internal medicine.

Structure

Major endocrine systems

The human endocrine system consists of several systems that operate via feedback loops. Several important feedback systems are mediated via the hypothalamus and pituitary.

Glands

Endocrine glands are glands of the endocrine system that secrete their products, hormones, directly into interstitial spaces where they are absorbed into blood rather than through a duct. The major glands of the endocrine system include the pineal gland, pituitary gland, pancreas, ovaries, testes, thyroid gland, parathyroid gland, hypothalamus and adrenal glands. The hypothalamus and pituitary gland are neuroendocrine organs.

The hypothalamus and the anterior pituitary are two out of the three endocrine glands that are important in cell signaling. They are both part of the HPA axis which is known to play a role in cell signaling in the nervous system.

Hypothalamus: The hypothalamus is a key regulator of the autonomic nervous system. The endocrine system has three sets of endocrine outputs which include the magnocellular system, the parvocellular system, and autonomic intervention. The magnocellular is involved in the expression of oxytocin or vasopressin. The parvocellular is involved in controlling the secretion of hormones from the anterior pituitary.

Anterior Pituitary: The main role of the anterior pituitary gland is to produce and secrete tropic hormones. Some examples of tropic hormones secreted by the anterior pituitary gland include TSH, ACTH, GH, LH, and FSH.

Endocrine cells

There are many types of cells that make up the endocrine system and these cells typically make up larger tissues and organs that function within and outside of the endocrine system.

Development

The fetal endocrine system is one of the first systems to develop during prenatal development.

Adrenal glands

The fetal adrenal cortex can be identified within four weeks of gestation. The adrenal cortex originates from the thickening of the intermediate mesoderm. At five to six weeks of gestation, the mesonephros differentiates into a tissue known as the genital ridge. The genital ridge produces the steroidogenic cells for both the gonads and the adrenal cortex. The adrenal medulla is derived from ectodermal cells. Cells that will become adrenal tissue move retroperitoneally to the upper portion of the mesonephros. At seven weeks of gestation, the adrenal cells are joined by sympathetic cells that originate from the neural crest to form the adrenal medulla. At the end of the eighth week, the adrenal glands have been encapsulated and have formed a distinct organ above the developing kidneys. At birth, the adrenal glands weigh approximately eight to nine grams (twice that of the adult adrenal glands) and are 0.5% of the total body weight. At 25 weeks, the adult adrenal cortex zone develops and is responsible for the primary synthesis of steroids during the early postnatal weeks.

Thyroid gland

The thyroid gland develops from two different clusterings of embryonic cells. One part is from the thickening of the pharyngeal floor, which serves as the precursor of the thyroxine (T4) producing follicular cells. The other part is from the caudal extensions of the fourth pharyngobranchial pouches which results in the parafollicular calcitonin-secreting cells. These two structures are apparent by 16 to 17 days of gestation. Around the 24th day of gestation, the foramen cecum, a thin, flask-like diverticulum of the median anlage develops. At approximately 24 to 32 days of gestation the median anlage develops into a bilobed structure. By 50 days of gestation, the medial and lateral anlage have fused together. At 12 weeks of gestation, the fetal thyroid is capable of storing iodine for the production of TRH, TSH, and free thyroid hormone. At 20 weeks, the fetus is able to implement feedback mechanisms for the production of thyroid hormones. During fetal development, T4 is the major thyroid hormone being produced while triiodothyronine (T3) and its inactive derivative, reverse T3, are not detected until the third trimester.

Parathyroid glands

A lateral and ventral view of an embryo showing the third (inferior) and fourth (superior) parathyroid glands during the 6th week of embryogenesis

Once the embryo reaches four weeks of gestation, the parathyroid glands begins to develop. The human embryo forms five sets of endoderm-lined pharyngeal pouches. The third and fourth pouch are responsible for developing into the inferior and superior parathyroid glands, respectively. The third pharyngeal pouch encounters the developing thyroid gland and they migrate down to the lower poles of the thyroid lobes. The fourth pharyngeal pouch later encounters the developing thyroid gland and migrates to the upper poles of the thyroid lobes. At 14 weeks of gestation, the parathyroid glands begin to enlarge from 0.1 mm in diameter to approximately 1 – 2 mm at birth. The developing parathyroid glands are physiologically functional beginning in the second trimester.

Studies in mice have shown that interfering with the HOX15 gene can cause parathyroid gland aplasia, which suggests the gene plays an important role in the development of the parathyroid gland. The genes, TBX1, CRKL, GATA3, GCM2, and SOX3 have also been shown to play a crucial role in the formation of the parathyroid gland. Mutations in TBX1 and CRKL genes are correlated with DiGeorge syndrome, while mutations in GATA3 have also resulted in a DiGeorge-like syndrome. Malformations in the GCM2 gene have resulted in hypoparathyroidism. Studies on SOX3 gene mutations have demonstrated that it plays a role in parathyroid development. These mutations also lead to varying degrees of hypopituitarism.

Pancreas

The human fetal pancreas begins to develop by the fourth week of gestation. Five weeks later, the pancreatic alpha and beta cells have begun to emerge. Reaching eight to ten weeks into development, the pancreas starts producing insulin, glucagon, somatostatin, and pancreatic polypeptide. During the early stages of fetal development, the number of pancreatic alpha cells outnumbers the number of pancreatic beta cells. The alpha cells reach their peak in the middle stage of gestation. From the middle stage until term, the beta cells continue to increase in number until they reach an approximate 1:1 ratio with the alpha cells. The insulin concentration within the fetal pancreas is 3.6 pmol/g at seven to ten weeks, which rises to 30 pmol/g at 16–25 weeks of gestation. Near term, the insulin concentration increases to 93 pmol/g. The endocrine cells have dispersed throughout the body within 10 weeks. At 31 weeks of development, the islets of Langerhans have differentiated.

While the fetal pancreas has functional beta cells by 14 to 24 weeks of gestation, the amount of insulin that is released into the bloodstream is relatively low. In a study of pregnant women carrying fetuses in the mid-gestation and near term stages of development, the fetuses did not have an increase in plasma insulin levels in response to injections of high levels of glucose. In contrast to insulin, the fetal plasma glucagon levels are relatively high and continue to increase during development. At the mid-stage of gestation, the glucagon concentration is 6 μg/g, compared to 2 μg/g in adult humans. Just like insulin, fetal glucagon plasma levels do not change in response to an infusion of glucose. However, a study of an infusion of alanine into pregnant women was shown to increase the cord blood and maternal glucagon concentrations, demonstrating a fetal response to amino acid exposure.

As such, while the fetal pancreatic alpha and beta islet cells have fully developed and are capable of hormone synthesis during the remaining fetal maturation, the islet cells are relatively immature in their capacity to produce glucagon and insulin. This is thought to be a result of the relatively stable levels of fetal serum glucose concentrations achieved via maternal transfer of glucose through the placenta. On the other hand, the stable fetal serum glucose levels could be attributed to the absence of pancreatic signaling initiated by incretins during feeding. In addition, the fetal pancreatic islets cells are unable to sufficiently produce cAMP and rapidly degrade cAMP by phosphodiesterase necessary to secrete glucagon and insulin.

During fetal development, the storage of glycogen is controlled by fetal glucocorticoids and placental lactogen. Fetal insulin is responsible for increasing glucose uptake and lipogenesis during the stages leading up to birth. Fetal cells contain a higher amount of insulin receptors in comparison to adults cells and fetal insulin receptors are not downregulated in cases of hyperinsulinemia. In comparison, fetal haptic glucagon receptors are lowered in comparison to adult cells and the glycemic effect of glucagon is blunted. This temporary physiological change aids the increased rate of fetal development during the final trimester. Poorly managed maternal diabetes mellitus is linked to fetal macrosomia, increased risk of miscarriage, and defects in fetal development. Maternal hyperglycemia is also linked to increased insulin levels and beta cell hyperplasia in the post-term infant. Children of diabetic mothers are at an increased risk for conditions such as: polycythemia, renal vein thrombosis, hypocalcemia, respiratory distress syndrome, jaundice, cardiomyopathy, congenital heart disease, and improper organ development.

Gonads

The reproductive system begins development at four to five weeks of gestation with germ cell migration. The bipotential gonad results from the collection of the medioventral region of the urogenital ridge. At the five-week point, the developing gonads break away from the adrenal primordium. Gonadal differentiation begins 42 days following conception.

Male gonadal development

For males, the testes form at six fetal weeks and the sertoli cells begin developing by the eight week of gestation. SRY, the sex-determining locus, serves to differentiate the Sertoli cells. The Sertoli cells are the point of origin for anti-Müllerian hormone. Once synthesized, the anti-Müllerian hormone initiates the ipsilateral regression of the Müllerian tract and inhibits the development of female internal features. At 10 weeks of gestation, the Leydig cells begin to produce androgen hormones. The androgen hormone dihydrotestosterone is responsible for the development of the male external genitalia.

The testicles descend during prenatal development in a two-stage process that begins at eight weeks of gestation and continues through the middle of the third trimester. During the transabdominal stage (8 to 15 weeks of gestation), the gubernacular ligament contracts and begins to thicken. The craniosuspensory ligament begins to break down. This stage is regulated by the secretion of insulin-like 3 (INSL3), a relaxin-like factor produced by the testicles, and the INSL3 G-coupled receptor, LGR8. During the transinguinal phase (25 to 35 weeks of gestation), the testicles descend into the scrotum. This stage is regulated by androgens, the genitofemoral nerve, and calcitonin gene-related peptide. During the second and third trimester, testicular development concludes with the diminution of the fetal Leydig cells and the lengthening and coiling of the seminiferous cords.

Female gonadal development

For females, the ovaries become morphologically visible by the 8th week of gestation. The absence of testosterone results in the diminution of the Wolffian structures. The Müllerian structures remain and develop into the fallopian tubes, uterus, and the upper region of the vagina. The urogenital sinus develops into the urethra and lower region of the vagina, the genital tubercle develops into the clitoris, the urogenital folds develop into the labia minora, and the urogenital swellings develop into the labia majora. At 16 weeks of gestation, the ovaries produce FSH and LH/hCG receptors. At 20 weeks of gestation, the theca cell precursors are present and oogonia mitosis is occurring. At 25 weeks of gestation, the ovary is morphologically defined and folliculogenesis can begin.

Studies of gene expression show that a specific complement of genes, such as follistatin and multiple cyclin kinase inhibitors are involved in ovarian development. An assortment of genes and proteins - such as WNT4, RSPO1, FOXL2, and various estrogen receptors - have been shown to prevent the development of testicles or the lineage of male-type cells.

Pituitary gland

The pituitary gland is formed within the rostral neural plate. The Rathke's pouch, a cavity of ectodermal cells of the oropharynx, forms between the fourth and fifth week of gestation and upon full development, it gives rise to the anterior pituitary gland. By seven weeks of gestation, the anterior pituitary vascular system begins to develop. During the first 12 weeks of gestation, the anterior pituitary undergoes cellular differentiation. At 20 weeks of gestation, the hypophyseal portal system has developed. The Rathke's pouch grows towards the third ventricle and fuses with the diverticulum. This eliminates the lumen and the structure becomes Rathke's cleft. The posterior pituitary lobe is formed from the diverticulum. Portions of the pituitary tissue may remain in the nasopharyngeal midline. In rare cases this results in functioning ectopic hormone-secreting tumors in the nasopharynx.

The functional development of the anterior pituitary involves spatiotemporal regulation of transcription factors expressed in pituitary stem cells and dynamic gradients of local soluble factors. The coordination of the dorsal gradient of pituitary morphogenesis is dependent on neuroectodermal signals from the infundibular bone morphogenetic protein 4 (BMP4). This protein is responsible for the development of the initial invagination of the Rathke's pouch. Other essential proteins necessary for pituitary cell proliferation are Fibroblast growth factor 8 (FGF8), Wnt4, and Wnt5. Ventral developmental patterning and the expression of transcription factors is influenced by the gradients of BMP2 and sonic hedgehog protein (SHH). These factors are essential for coordinating early patterns of cell proliferation.

Six weeks into gestation, the corticotroph cells can be identified. By seven weeks of gestation, the anterior pituitary is capable of secreting ACTH. Within eight weeks of gestation, somatotroph cells begin to develop with cytoplasmic expression of human growth hormone. Once a fetus reaches 12 weeks of development, the thyrotrophs begin expression of Beta subunits for TSH, while gonadotrophs being to express beta-subunits for LH and FSH. Male fetuses predominately produced LH-expressing gonadotrophs, while female fetuses produce an equal expression of LH and FSH expressing gonadotrophs. At 24 weeks of gestation, prolactin-expressing lactotrophs begin to emerge.

Function

Hormones

A hormone is any of a class of signaling molecules produced by cells in glands in multicellular organisms that are transported by the circulatory system to target distant organs to regulate physiology and behaviour. Hormones have diverse chemical structures, mainly of 3 classes: eicosanoids, steroids, and amino acid/protein derivatives (amines, peptides, and proteins). The glands that secrete hormones comprise the endocrine system. The term hormone is sometimes extended to include chemicals produced by cells that affect the same cell (autocrine or intracrine signalling) or nearby cells (paracrine signalling).

Hormones are used to communicate between organs and tissues for physiological regulation and behavioral activities, such as digestion, metabolism, respiration, tissue function, sensory perception, sleep, excretion, lactation, stress, growth and development, movement, reproduction, and mood.

Hormones affect distant cells by binding to specific receptor proteins in the target cell resulting in a change in cell function. This may lead to cell type-specific responses that include rapid changes to the activity of existing proteins, or slower changes in the expression of target genes. Amino acid–based hormones (amines and peptide or protein hormones) are water-soluble and act on the surface of target cells via signal transduction pathways; steroid hormones, being lipid-soluble, move through the plasma membranes of target cells to act within their nuclei.

Cell signalling

The typical mode of cell signalling in the endocrine system is endocrine signaling, that is, using the circulatory system to reach distant target organs. However, there are also other modes, i.e., paracrine, autocrine, and neuroendocrine signaling. Purely neurocrine signaling between neurons, on the other hand, belongs completely to the nervous system.

Autocrine

Autocrine signaling is a form of signaling in which a cell secretes a hormone or chemical messenger (called the autocrine agent) that binds to autocrine receptors on the same cell, leading to changes in the cells.

Paracrine

Some endocrinologists and clinicians include the paracrine system as part of the endocrine system, but there is not consensus. Paracrines are slower acting, targeting cells in the same tissue or organ. An example of this is somatostatin which is released by some pancreatic cells and targets other pancreatic cells.

Juxtacrine

Juxtacrine signaling is a type of intercellular communication that is transmitted via oligosaccharide, lipid, or protein components of a cell membrane, and may affect either the emitting cell or the immediately adjacent cells.

It occurs between adjacent cells that possess broad patches of closely opposed plasma membrane linked by transmembrane channels known as connexons. The gap between the cells can usually be between only 2 and 4 nm.

Clinical significance

Disease

Diseases of the endocrine system are common, including conditions such as diabetes mellitus, thyroid disease, and obesity. Endocrine disease is characterized by misregulated hormone release (a productive pituitary adenoma), inappropriate response to signaling (hypothyroidism), lack of a gland (diabetes mellitus type 1, diminished erythropoiesis in chronic kidney failure), or structural enlargement in a critical site such as the thyroid (toxic multinodular goitre). Hypofunction of endocrine glands can occur as a result of loss of reserve, hyposecretion, agenesis, atrophy, or active destruction. Hyperfunction can occur as a result of hypersecretion, loss of suppression, hyperplastic or neoplastic change, or hyperstimulation.

Endocrinopathies are classified as primary, secondary, or tertiary. Primary endocrine disease inhibits the action of downstream glands. Secondary endocrine disease is indicative of a problem with the pituitary gland. Tertiary endocrine disease is associated with dysfunction of the hypothalamus and its releasing hormones.

As the thyroid, and hormones have been implicated in signaling distant tissues to proliferate, for example, the estrogen receptor has been shown to be involved in certain breast cancers. Endocrine, paracrine, and autocrine signaling have all been implicated in proliferation, one of the required steps of oncogenesis.

Other common diseases that result from endocrine dysfunction include Addison's disease, Cushing's disease and Graves' disease. Cushing's disease and Addison's disease are pathologies involving the dysfunction of the adrenal gland. Dysfunction in the adrenal gland could be due to primary or secondary factors and can result in hypercortisolism or hypocortisolism. Cushing's disease is characterized by the hypersecretion of the adrenocorticotropic hormone (ACTH) due to a pituitary adenoma that ultimately causes endogenous hypercortisolism by stimulating the adrenal glands. Some clinical signs of Cushing's disease include obesity, moon face, and hirsutism. Addison's disease is an endocrine disease that results from hypocortisolism caused by adrenal gland insufficiency. Adrenal insufficiency is significant because it is correlated with decreased ability to maintain blood pressure and blood sugar, a defect that can prove to be fatal.

Graves' disease involves the hyperactivity of the thyroid gland which produces the T3 and T4 hormones. Graves' disease effects range from excess sweating, fatigue, heat intolerance and high blood pressure to swelling of the eyes that causes redness, puffiness and in rare cases reduced or double vision.

DALY rates

Disability-adjusted life year for endocrine disorders per 100,000 inhabitants in 2002.
  No data
  Less than 80
  80–160
  160–240
  240–320
  320–400
  400–480
  480–560
  560–640
  640–720
  720–800
  800–1000
  More than 1000


A DALY (Disability-Adjusted Life Year) is a measure that reflects the total burden of disease. It combines years of life lost (due to premature death) and years lived with disability (adjusted for the severity of the disability). The lower the DALY rates, the lower the burden of endocrine disorders in a country.

The map shows that large parts of Asia have lower DALY rates (pale yellow), suggesting that endocrine disorders have a relatively low impact on overall health, whereas some countries in South America and Africa (specifically Suriname and Somalia) have higher DALY rates (dark orange to red), indicating a higher disease burden from endocrine disorders.

Other animals

A neuroendocrine system has been observed in all animals with a nervous system and all vertebrates have a hypothalamus–pituitary axis. All vertebrates have a thyroid, which in amphibians is also crucial for transformation of larvae into adult form. All vertebrates have adrenal gland tissue, with mammals unique in having it organized into layers. All vertebrates have some form of a renin–angiotensin axis, and all tetrapods have aldosterone as a primary mineralocorticoid.

History of religion in the United States

From Wikipedia, the free encyclopedia https://en.wikipedia.org/wiki/History_of_religion_in_the_Un...