Mercuric amidochloride is an inorganic compound with the formula HgNH2Cl. It consists of a zig-zag 1-dimensional polymer n with chloride counterions, it arises from the reaction of ammonia and mercuric chloride. Addition of base converts it into "Millon's base,". A variety of related amido and nitrido materials with chloride and hydroxide are known. Before the toxicity of mercury was appreciated, mercuric amidochloride, known as "ammoniated mercury", was used as a topical antiseptic and disinfectant. Merbromin known as "Mercurochrome", another antiseptic mercury compound Thiomersal, another antiseptic mercury compound
Mercury oxide called mercuric oxide or mercury oxide, has a formula of HgO. It has a orange color. Mercury oxide is a solid at room pressure; the mineral form montroydite is rarely found. In 1774, Joseph Priestley discovered that oxygen was released by heating mercuric oxide, although he did not identify the gas as oxygen; the red form of HgO can be made by heating Hg in oxygen at 350 °C, or by pyrolysis of Hg2. The yellow form can be obtained by precipitation of aqueous Hg2+ with alkali; the difference in color is due to particle size, both forms have the same structure consisting of near linear O-Hg-O units linked in zigzag chains with an Hg-O-Hg angle of 108°. Under atmospheric pressure mercuric oxide has two crystalline forms: one is called montroydite, the second is analogous to the sulfide mineral cinnabar. At pressures above 10 GPa both structures convert to a tetragonal form. HgO is sometimes used in the production of mercury; when it decomposes, oxygen gas is generated. It is used as a material for cathodes for mercury batteries.
Mercury oxide is a toxic substance which can be absorbed into the body by inhalation of its aerosol, through the skin and by ingestion. The substance is irritating to the eyes, the skin and the respiratory tract and may have effects on the kidneys, resulting in kidney impairment. In the food chain important to humans, bioaccumulation takes place in aquatic organisms; the substance is banned as a pesticide in the EU. Evaporation at 20 °C is negligible. HgO decomposes on exposure to light or on heating above 500 °C. Heating produces toxic mercury fumes and oxygen, which increases the fire hazard. Mercury oxide reacts violently with reducing agents, hydrogen peroxide, disulfur dichloride and hydrogen trisulfide. Shock-sensitive compounds are formed with elements such as sulfur and phosphorus. National Pollutant Inventory – Mercury and compounds fact sheet Information at Webelements
Mercury sulfide, mercuric sulfide, mercury sulphide, or mercury sulfide is a chemical compound composed of the chemical elements mercury and sulfur. It is represented by the chemical formula HgS, it is insoluble in water. HgS is dimorphic with two crystal forms: red cinnabar, is the form in which mercury is most found in nature. Black, adopts the zinc blende crystal structure. Crystals of red, α-HgS, are optically active; this is caused by the Hg-S helices in the structure. Β-HgS is precipitated as a black powder. Β-HgS is unreactive to all but concentrated acids. Mercury metal is produced from the cinnabar ore by condensing the vapour; when α-HgS is used as a red pigment, it is known as vermilion. The tendency of vermilion to darken has been ascribed to conversion from red α-HgS to black β-HgS; however β-HgS was not detected at excavations in Pompeii, where red walls darkened, was attributed to the formation of Hg-Cl compounds and calcium sulfate, gypsum. Cinnabar Mercury poisoning Mercury sulfide, Hg2S
Redox is a chemical reaction in which the oxidation states of atoms are changed. Any such reaction involves both a reduction process and a complementary oxidation process, two key concepts involved with electron transfer processes. Redox reactions include all chemical reactions; the chemical species from which the electron is stripped is said to have been oxidized, while the chemical species to which the electron is added is said to have been reduced. It can be explained in simple terms: Oxidation is the loss of electrons or an increase in oxidation state by a molecule, atom, or ion. Reduction is a decrease in oxidation state by a molecule, atom, or ion; as an example, during the combustion of wood, oxygen from the air is reduced, gaining electrons from carbon, oxidized. Although oxidation reactions are associated with the formation of oxides from oxygen molecules, oxygen is not included in such reactions, as other chemical species can serve the same function; the reaction can occur slowly, as with the formation of rust, or more in the case of fire.
There are simple redox processes, such as the oxidation of carbon to yield carbon dioxide or the reduction of carbon by hydrogen to yield methane, more complex processes such as the oxidation of glucose in the human body. "Redox" is a portmanteau of the words "reduction" and "oxidation". The word oxidation implied reaction with oxygen to form an oxide, since dioxygen was the first recognized oxidizing agent; the term was expanded to encompass oxygen-like substances that accomplished parallel chemical reactions. The meaning was generalized to include all processes involving loss of electrons; the word reduction referred to the loss in weight upon heating a metallic ore such as a metal oxide to extract the metal. In other words, ore was "reduced" to metal. Antoine Lavoisier showed. Scientists realized that the metal atom gains electrons in this process; the meaning of reduction became generalized to include all processes involving a gain of electrons. Though "reduction" seems counter-intuitive when speaking of the gain of electrons, it might help to think of reduction as the loss of oxygen, its historical meaning.
Since electrons are negatively charged, it is helpful to think of this as reduction in electrical charge. The electrochemist John Bockris has used the words electronation and deelectronation to describe reduction and oxidation processes when they occur at electrodes; these words are analogous to protonation and deprotonation, but they have not been adopted by chemists worldwide. The term "hydrogenation" could be used instead of reduction, since hydrogen is the reducing agent in a large number of reactions in organic chemistry and biochemistry. But, unlike oxidation, generalized beyond its root element, hydrogenation has maintained its specific connection to reactions that add hydrogen to another substance; the word "redox" was first used in 1928. The processes of oxidation and reduction occur and cannot happen independently of one another, similar to the acid–base reaction; the oxidation alone and the reduction alone are each called a half-reaction, because two half-reactions always occur together to form a whole reaction.
When writing half-reactions, the gained or lost electrons are included explicitly in order that the half-reaction be balanced with respect to electric charge. Though sufficient for many purposes, these general descriptions are not correct. Although oxidation and reduction properly refer to a change in oxidation state — the actual transfer of electrons may never occur; the oxidation state of an atom is the fictitious charge that an atom would have if all bonds between atoms of different elements were 100% ionic. Thus, oxidation is best defined as an increase in oxidation state, reduction as a decrease in oxidation state. In practice, the transfer of electrons will always cause a change in oxidation state, but there are many reactions that are classed as "redox" though no electron transfer occurs. In redox processes, the reductant transfers electrons to the oxidant. Thus, in the reaction, the reductant or reducing agent loses electrons and is oxidized, the oxidant or oxidizing agent gains electrons and is reduced.
The pair of an oxidizing and reducing agent that are involved in a particular reaction is called a redox pair. A redox couple is a reducing species and its corresponding oxidizing form, e.g. Fe2+/Fe3+ Substances that have the ability to oxidize other substances are said to be oxidative or oxidizing and are known as oxidizing agents, oxidants, or oxidizers; that is, the oxidant removes electrons from another substance, is thus itself reduced. And, because it "accepts" electrons, the oxidizing agent is called an electron acceptor. Oxygen is the quintessential oxidizer. Oxidants are chemical substances with elements in high oxidation states, or else electronegative elements that can gain extra electrons by oxidizing another substance. Substances that have the ability to reduce other substances are said to be reductive or reducing and are known as
Mercury is a chemical element with symbol Hg and atomic number 80. It is known as quicksilver and was named hydrargyrum. A heavy, silvery d-block element, mercury is the only metallic element, liquid at standard conditions for temperature and pressure. Mercury occurs in deposits throughout the world as cinnabar; the red pigment vermilion is obtained by synthetic mercuric sulfide. Mercury is used in thermometers, manometers, sphygmomanometers, float valves, mercury switches, mercury relays, fluorescent lamps and other devices, though concerns about the element's toxicity have led to mercury thermometers and sphygmomanometers being phased out in clinical environments in favor of alternatives such as alcohol- or galinstan-filled glass thermometers and thermistor- or infrared-based electronic instruments. Mechanical pressure gauges and electronic strain gauge sensors have replaced mercury sphygmomanometers. Mercury remains in use in scientific research applications and in amalgam for dental restoration in some locales.
It is used in fluorescent lighting. Electricity passed through mercury vapor in a fluorescent lamp produces short-wave ultraviolet light, which causes the phosphor in the tube to fluoresce, making visible light. Mercury poisoning can result from exposure to water-soluble forms of mercury, by inhalation of mercury vapor, or by ingesting any form of mercury. Mercury is a silvery-white liquid metal. Compared to other metals, it is a fair conductor of electricity, it has a freezing point of −38.83 °C and a boiling point of 356.73 °C, both the lowest of any stable metal, although preliminary experiments on copernicium and flerovium have indicated that they have lower boiling points. Upon freezing, the volume of mercury decreases by 3.59% and its density changes from 13.69 g/cm3 when liquid to 14.184 g/cm3 when solid. The coefficient of volume expansion is 181.59 × 10−6 at 0 °C, 181.71 × 10−6 at 20 °C and 182.50 × 10−6 at 100 °C. Solid mercury can be cut with a knife. A complete explanation of mercury's extreme volatility delves deep into the realm of quantum physics, but it can be summarized as follows: mercury has a unique electron configuration where electrons fill up all the available 1s, 2s, 2p, 3s, 3p, 3d, 4s, 4p, 4d, 4f, 5s, 5p, 5d, 6s subshells.
Because this configuration resists removal of an electron, mercury behaves to noble gases, which form weak bonds and hence melt at low temperatures. The stability of the 6s shell is due to the presence of a filled 4f shell. An f shell poorly screens the nuclear charge that increases the attractive Coulomb interaction of the 6s shell and the nucleus; the absence of a filled inner f shell is the reason for the somewhat higher melting temperature of cadmium and zinc, although both these metals still melt and, in addition, have unusually low boiling points. Mercury does not react with most acids, such as dilute sulfuric acid, although oxidizing acids such as concentrated sulfuric acid and nitric acid or aqua regia dissolve it to give sulfate and chloride. Like silver, mercury reacts with atmospheric hydrogen sulfide. Mercury reacts with solid sulfur flakes. Mercury dissolves many metals such as silver to form amalgams. Iron is an exception, iron flasks have traditionally been used to trade mercury.
Several other first row transition metals with the exception of manganese and zinc are resistant in forming amalgams. Other elements that do not form amalgams with mercury include platinum. Sodium amalgam is a common reducing agent in organic synthesis, is used in high-pressure sodium lamps. Mercury combines with aluminium to form a mercury-aluminium amalgam when the two pure metals come into contact. Since the amalgam destroys the aluminium oxide layer which protects metallic aluminium from oxidizing in-depth small amounts of mercury can corrode aluminium. For this reason, mercury is not allowed aboard an aircraft under most circumstances because of the risk of it forming an amalgam with exposed aluminium parts in the aircraft. Mercury embrittlement is the most common type of liquid metal embrittlement. There are seven stable isotopes of mercury, with 202Hg being the most abundant; the longest-lived radioisotopes are 194Hg with a half-life of 444 years, 203Hg with a half-life of 46.612 days. Most of the remaining radioisotopes have half-lives.
199Hg and 201Hg are the most studied NMR-active nuclei, having spins of 1⁄2 and 3⁄2 respectively. Hg is the modern chemical symbol for mercury, it comes from hydrargyrum, a Latinized form of the Greek word ὑδράργυρος, a compound word meaning "water-silver" – since it is liquid like water and shiny like silver. The element was named after the Roman god Mercury, known for his mobility, it is associated with the planet Mercury. Mercury is the only metal for which the al
Mercury fulminate, or Hg2, is a primary explosive. It is sensitive to friction and shock and is used as a trigger for other explosives in percussion caps and blasting caps. Mercury cyanate, though its empirical formula is identical, has a different atomic arrangement. First used as a priming composition in small copper caps beginning in the 1820s, mercury fulminate replaced flints as a means to ignite black powder charges in muzzle-loading firearms. During the late 19th century and most of the 20th century, mercury fulminate or potassium chlorate became used in primers for self-contained rifle and pistol ammunition. Mercury fulminate has the distinct advantage over potassium chlorate of being non-corrosive, but it is known to weaken with time, by decomposing into its constituent elements; the reduced mercury which results forms amalgams with cartridge brass, as well. Today, mercury fulminate has been replaced in primers by more efficient chemical substances; these are less toxic and more stable over time.
In addition, none of these compounds require mercury for manufacture, supplies of which can be unreliable in wartime. Mercury fulminate is prepared by dissolving mercury in nitric acid and adding ethanol to the solution, it was first prepared by Edward Charles Howard in 1800. The crystal structure of this compound was only determined in 2007. Silver fulminate can be prepared in a similar way, but this salt is more unstable than mercury fulminate; the thermal decomposition of mercury fulminate can begin at temperatures as low as 100 °C, though it proceeds at a much higher rate with increasing temperature. A possible reaction for the decomposition of mercury fulminate yields carbon dioxide gas, nitrogen gas, a combination of stable mercury salts. 4 Hg2 → 2 CO2 + N2 + HgO + 3 HgCN Hg2 → 2 CO + N2 + Hg Hg2 →:Hg2 2 Hg2 → 2 CO2 + N2 + Hg + Hg2 Fulminic acid Potassium fulminate National Pollutant Inventory - Mercury and compounds Fact Sheet "300 years after discovery, structure of mercury fulminate determined".
Physorg.com. 24 August 2007
The electron is a subatomic particle, symbol e− or β−, whose electric charge is negative one elementary charge. Electrons belong to the first generation of the lepton particle family, are thought to be elementary particles because they have no known components or substructure; the electron has a mass, 1/1836 that of the proton. Quantum mechanical properties of the electron include an intrinsic angular momentum of a half-integer value, expressed in units of the reduced Planck constant, ħ; as it is a fermion, no two electrons can occupy the same quantum state, in accordance with the Pauli exclusion principle. Like all elementary particles, electrons exhibit properties of both particles and waves: they can collide with other particles and can be diffracted like light; the wave properties of electrons are easier to observe with experiments than those of other particles like neutrons and protons because electrons have a lower mass and hence a longer de Broglie wavelength for a given energy. Electrons play an essential role in numerous physical phenomena, such as electricity, magnetism and thermal conductivity, they participate in gravitational and weak interactions.
Since an electron has charge, it has a surrounding electric field, if that electron is moving relative to an observer, it will generate a magnetic field. Electromagnetic fields produced from other sources will affect the motion of an electron according to the Lorentz force law. Electrons absorb energy in the form of photons when they are accelerated. Laboratory instruments are capable of trapping individual electrons as well as electron plasma by the use of electromagnetic fields. Special telescopes can detect electron plasma in outer space. Electrons are involved in many applications such as electronics, cathode ray tubes, electron microscopes, radiation therapy, gaseous ionization detectors and particle accelerators. Interactions involving electrons with other subatomic particles are of interest in fields such as chemistry and nuclear physics; the Coulomb force interaction between the positive protons within atomic nuclei and the negative electrons without, allows the composition of the two known as atoms.
Ionization or differences in the proportions of negative electrons versus positive nuclei changes the binding energy of an atomic system. The exchange or sharing of the electrons between two or more atoms is the main cause of chemical bonding. In 1838, British natural philosopher Richard Laming first hypothesized the concept of an indivisible quantity of electric charge to explain the chemical properties of atoms. Irish physicist George Johnstone Stoney named this charge'electron' in 1891, J. J. Thomson and his team of British physicists identified it as a particle in 1897. Electrons can participate in nuclear reactions, such as nucleosynthesis in stars, where they are known as beta particles. Electrons can be created through beta decay of radioactive isotopes and in high-energy collisions, for instance when cosmic rays enter the atmosphere; the antiparticle of the electron is called the positron. When an electron collides with a positron, both particles can be annihilated, producing gamma ray photons.
The ancient Greeks noticed. Along with lightning, this phenomenon is one of humanity's earliest recorded experiences with electricity. In his 1600 treatise De Magnete, the English scientist William Gilbert coined the New Latin term electrica, to refer to those substances with property similar to that of amber which attract small objects after being rubbed. Both electric and electricity are derived from the Latin ēlectrum, which came from the Greek word for amber, ἤλεκτρον. In the early 1700s, Francis Hauksbee and French chemist Charles François du Fay independently discovered what they believed were two kinds of frictional electricity—one generated from rubbing glass, the other from rubbing resin. From this, du Fay theorized that electricity consists of two electrical fluids and resinous, that are separated by friction, that neutralize each other when combined. American scientist Ebenezer Kinnersley also independently reached the same conclusion. A decade Benjamin Franklin proposed that electricity was not from different types of electrical fluid, but a single electrical fluid showing an excess or deficit.
He gave them the modern charge nomenclature of negative respectively. Franklin thought of the charge carrier as being positive, but he did not identify which situation was a surplus of the charge carrier, which situation was a deficit. Between 1838 and 1851, British natural philosopher Richard Laming developed the idea that an atom is composed of a core of matter surrounded by subatomic particles that had unit electric charges. Beginning in 1846, German physicist William Weber theorized that electricity was composed of positively and negatively charged fluids, their interaction was governed by the inverse square law. After studying the phenomenon of electrolysis in 1874, Irish physicist George Johnstone Stoney suggested that there existed a "single definite quantity of electricity", the charge of a monovalent ion, he was able to estimate the value of this elementary charge e by means of Faraday's laws of electrolysis. However, Stoney could not be removed. In 1881, German physicist Hermann von Helmholtz argued that both positive and negative charges were divided into elementary parts, each of which "behaves like atoms of electricity".
Stoney coined the term