Introduction

Phosphorus

The principal method for producing phosphorus is to reduce phosphates with carbon in an electric arc furnace.

Elemental phosphorus was first isolated as white phosphorus in 1669. In white phosphorus, phosphorus atoms are arranged in groups of 4, written as P4. White phosphorus emits a faint glow when exposed to oxygen—hence a name, taken from Greek mythology, Φωσφόρος meaning 'light-bearer' (Latin Lucifer), referring to the "Morning Star", the planet Venus. The term phosphorescence, meaning glow after illumination, has its origin in phosphorus, although phosphorus itself does not exhibit phosphorescence: phosphorus glows due to oxidation of the white (but not red) phosphorus—a process now called chemiluminescence. Phosphorus is classified as a pnictogen, together with nitrogen, arsenic, antimony, bismuth, and moscovium.

Phosphorus is an element essential to sustaining life largely through phosphates, compounds containing the phosphate ion, PO43−. Phosphates are a component of DNA, RNA, ATP, and phospholipids, complex compounds fundamental to cells. Elemental phosphorus was first isolated from human urine, and bone ash was an important early phosphate source. Phosphate mines contain fossils because phosphate is present in the fossilized deposits of animal remains and excreta. Low phosphate levels are an important limit to growth in a number of plant ecosystems. The vast majority of phosphorus compounds mined are consumed as fertilisers. Phosphate is needed to replace the phosphorus that plants remove from the soil, and its annual demand is rising nearly twice as fast as the growth of the human population. Other applications include organophosphorus compounds in detergents, pesticides, and nerve agents.

Nitrogen

Nitrogen can be produced by fractional distillation of air. Nitrogen can also be produced in a large scale by burning hydrocarbons or hydrogen in air. On a smaller scale, it is also possible to make nitrogen by heating barium azide. Additionally, the following reactions produce nitrogen: NH4+ + NO2 − → N2 + 2H2O 8NH3 + 3Br2 → N2 + 6NH4 + + 6Br− 2NH3 + 3CuO → N2 + 3H2O + 2Cu 

It was first discovered and isolated by Scottish physician Daniel Rutherford in 1772 and independently by Carl Wilhelm Scheele and Henry Cavendish at about the same time. The name nitrogène was suggested by French chemist Jean-Antoine-Claude Chaptal in 1790 when it was found that nitrogen was present in nitric acid and nitrates. Antoine Lavoisier suggested instead the name azote, from the Ancient Greek: ἀζωτικός "no life", as it is an asphyxiant gas; this name is used in a number of languages, and appears in the English names of some nitrogen compounds such as hydrazine, azides and azo compounds.

Elemental nitrogen is usually produced from air by pressure swing adsorption technology. About 2/3 of commercially produced elemental nitrogen is used as an inert (oxygen-free) gas for commercial uses such as food packaging, and much of the rest is used as liquid nitrogen in cryogenic applications. Many industrially important compounds, such as ammonia, nitric acid, organic nitrates (propellants and explosives), and cyanides, contain nitrogen. The extremely strong triple bond in elemental nitrogen (N≡N), the second strongest bond in any diatomic molecule after carbon monoxide (CO),[7] dominates nitrogen chemistry. This causes difficulty for both organisms and industry in converting N2 into useful compounds, but at the same time it means that burning, exploding, or decomposing nitrogen compounds to form nitrogen gas releases large amounts of often useful energy. Synthetically produced ammonia and nitrates are key industrial fertilisers, and fertiliser nitrates are key pollutants in the eutrophication of water systems. Apart from its use in fertilisers and energy stores, nitrogen is a constituent of organic compounds as diverse as aramids used in high-strength fabric and cyanoacrylate used in superglue.

Arsenic

Most arsenic is prepared by heating the mineral arsenopyrite in the presence of air. This forms As4O6, from which arsenic can be extracted via carbon reduction. However, it is also possible to make metallic arsenic by heating arsenopyrite at 650 to 700 °C without oxygen.

The primary use of arsenic is in alloys of lead (for example, in car batteries and ammunition). Arsenic is a common n-type dopant in semiconductor electronic devices. It is also a component of the III–V compound semiconductor gallium arsenide. Arsenic and its compounds, especially the trioxide, are used in the production of pesticides, treated wood products, herbicides, and insecticides. These applications are declining with the increasing recognition of the toxicity of arsenic and its compounds.[11]

A few species of bacteria are able to use arsenic compounds as respiratory metabolites. Trace quantities of arsenic may be an essential dietary element in rats, hamsters, goats, chickens, and presumably other species. A role in human metabolism is not known.[12][13] However, arsenic poisoning occurs in multicellular life if quantities are larger than needed. Arsenic contamination of groundwater is a problem that affects millions of people across the world.

The United States' Environmental Protection Agency states that all forms of arsenic are a serious risk to human health.[14] The United States' Agency for Toxic Substances and Disease Registry ranked arsenic number 1 in its 2001 prioritized list of hazardous substances at Superfund sites.[15] Arsenic is classified as a Group-A carcinogen.[14]

Antimony

With sulfide ores, the method by which antimony is produced depends on the amount of antimony in the raw ore. If the ore contains 25% to 45% antimony by weight, then crude antimony is produced by smelting the ore in a blast furnace. If the ore contains 45% to 60% antimony by weight, antimony is obtained by heating the ore, also known as liquidation. Ores with more than 60% antimony by weight are chemically displaced with iron shavings from the molten ore, resulting in impure metal.

If an oxide ore of antimony contains less than 30% antimony by weight, the ore is reduced in a blast furnace. If the ore contains closer to 50% antimony by weight, the ore is instead reduced in a reverberatory furnace

Antimony ores with mixed sulfides and oxides are smelted in a blast furnace

China is the largest producer of antimony and its compounds, with most production coming from the Xikuangshan Mine in Hunan. The industrial methods for refining antimony from stibnite are roasting followed by reduction with carbon, or direct reduction of stibnite with iron.

The most common applications for metallic antimony are in alloys with lead and tin, which have improved properties for solders, bullets, and plain bearings. It improves the rigidity of lead-alloy plates in lead–acid batteries. Antimony trioxide is a prominent additive for halogen-containing flame retardants. Antimony is used as a dopant in semiconductor devices.

Bismuth

Bismuth minerals do occur, but it is more economic to produce bismuth as a by-product of lead. In China, bismuth is also found in tungsten and zinc ores 

Bismuth used to be considered the element with the highest atomic mass whose nuclei do not spontaneously decay. However, in 2003 it was discovered to be extremely weakly radioactive. The metal's only primordial isotope, bismuth-209, undergoes alpha decay with a half-life about a billion times the estimated age of the universe.[7][8]

Bismuth metal has been known since ancient times. Before modern analytical methods bismuth's metallurgical similarities to lead and tin often led it to be confused with those metals. The etymology of "bismuth" is uncertain. The name may come from mid-sixteenth century Neo-Latin translations of the German words weiße Masse or Wismuth, meaning 'white mass', which were rendered as bisemutum or bisemutium.

Bismuth compounds account for about half the global production of bismuth. They are used in cosmetics; pigments; and a few pharmaceuticals, notably bismuth subsalicylate, used to treat diarrhea.[8] Bismuth's unusual propensity to expand as it solidifies is responsible for some of its uses, as in the casting of printing type.[8] Bismuth, when in its elemental form, has unusually low toxicity for a heavy metal.[8] As the toxicity of lead and the cost of its environmental remediation became more apparent during the 20th century, suitable bismuth alloys have gained popularity as replacements for lead. Presently, around a third of global bismuth production is dedicated to needs formerly met by lead.