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Oxygen

Oxygen [O]
CAS-ID: 7782-44-7
An: 8 N: 8
Am: 15.9994 (3) g/mol
Group No: 16
Group Name: Chalcogen
Block: p-block Period: 2
State: gas at 298 K
Colour: colourless as a gas, liquid is pale blue Classification: Non-metallic
Boiling Point: 90.2K (-182.9°C)
Melting Point: 54.8K (-218.3°C)
Critical temperature: 154.6K (-118.5°C)
Density: 1.429g/l

Discovery Information
Who: Joseph Priestley, Karl Wilhelm Scheele
When: 1774
Where: England/Sweden

Name Origin
Greek: oxus (acid) and gennan (generate).

Sources
Obtained primarily from by liquification and then fractional distillation of the air. World wide production is around 100 million tons.

Abundance
Universe: 10000 ppm (by weight)
Sun: 9000 ppm (by weight)
Carbonaceous meteorite: 4.1 x 105 ppm
Atmosphere: 2.095 x 105 ppm
Earth's Crust: 4.74 x 105 ppm
Human:
6.1 x 108 ppb by weight
2.4 x 108 ppb by atoms

Uses
Used in steel making, production of methanol (CH3OH), welding, water purification, cement and rocket propulsion. It is also required for supporting life and combustion. Oxygen is a major component of air, produced by plants during photosynthesis, and is necessary for aerobic respiration in animals.

History
Oxygen was first described by Michal Sedziwoj, a Polish alchemist and philosopher in the late 16th century. Sedziwoj thought of the gas given off by warm niter (saltpeter) as "the elixir of life".

Oxygen was more quantitatively discovered by the Swedish pharmacist Karl Wilhelm Scheele some time before 1773, but the discovery was not published until after the independent discovery by Joseph Priestley on August 1, 1774, who called the gas dephlogisticated air. Priestley published discoveries in 1775 and Scheele in 1777; consequently Priestley is usually given the credit. Both Scheele and Priestley produced oxygen by heating mercuric oxide.

Scheele called the gas 'fire air' because it was the only known supporter of combustion. It was later called 'vital air' because it was and is vital for the existence of animal life.

The gas was named by Antoine Laurent Lavoisier, after Priestley's publication in 1775, from Greek roots meaning "acid-former". As noted, the name reflects the then-common incorrect belief that all acids contain oxygen. This is also the origin of the Japanese name of oxygen "sanso" (san=acid, so=element).

Oxygen was first time condensed in 1883 by professors of Jagiellonian University - Zygmunt Wroblewski (Polish chemist) Karol Olszewski (Polish physicist and chemist).

Notes
Liquid and solid O2 are both a light blue colour. Ozone (O3) is a deeper blue colour. Oxygen is the second most common element on Earth, composing around 46% of the mass of Earth's crust (the most common element) and 28% of the mass of Earth as a whole, and is the third most common element in the universe. Forms almost 21% of atmosphere.

Hazards
Certain derivatives of oxygen, such as ozone (O3), singlet oxygen, hydrogen peroxide (H2O2), hydroxyl radicals and superoxide (O2-), are highly toxic. Highly concentrated sources of oxygen promote rapid combustion and therefore are fire and explosion hazards in the presence of fuels.
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Boron

Boron [B]
CAS-ID: 7440-42-8
An: 5 N: 6
Am: 10.811 (7) g/mol
Group No: 13
Group Name: Metalloids
Block: p-block Period: 2
State: solid
Colour: black Classification: Semi-metallic
Boiling Point: 4200K (3927°C)
Melting Point: 2349K (2076°C)
Density: 2.34g/cm3

Discovery Information
Who: H. Davy, J.L. Gay-Lussac, L.J. Thenard
When: 1828
Where: England/France

Name Origin
From borax and carbon.

Sources
Obtained from kernite, a kind of borax (Na2B4O7.10H2O). The world wide commercial borate deposits are estimated to be 1010 kg of boron.

The USA, Tibet, Chile and Turkey are important producers. Around 1 million tons of boric anhydride (B2O3) are produced each year.

Abundance
Universe: 0.001 ppm (by weight)
Sun: 0.002 ppm (by weight)
Carbonaceous meteorite: 1.6 ppm
Earth's Crust: 950 ppm
Seawater: 4.41 ppm

Human:
700 ppb by weight
410 ppb by atoms

Uses
Used with titanium and tungsten to make light weight heat resistant alloys. Also tennis rackets, regulators in nuclear plants, heat resistant glass and eye disinfectant. Boric acid (H3BO3) is used an insectiside, mostly against ants or cockroaches.

Boron nitride is a material in which the extra electron of nitrogen (with respect to carbon) enables it to form structures that are isoelectronic with carbon allotropes.

Sodium tetraborate decahydrate (Na2B4O7 - 10H2O) or borax, used in the production of adhesives, in anti-corrosion systems and many other uses.

Sodium tetraborate pentahydrate (Na2B4O7 - 5H2O), which is used in large amounts in making insulating fiberglass and sodium perborate bleach.

Orthoboric acid (H3BO3) or boric acid is used in the production of textile fiberglass, flat panel displays and eye drops.

Boron slurry is used as an energetic material with very high energy density like rocket fuels and jet engines.

History
Compounds of boron have been known of for thousands of years. In early Egypt, mummification depended upon an ore known as natron, which contained borates as well as some other common salts. Borax glazes were used in China from 300 AD, and boron compounds were used in glassmaking in ancient Rome.

The element was not isolated until 1808 by Sir Humphry Davy, Joseph Louis Gay-Lussac, and Louis Jacques Thenard, to about 50 percent purity, by the reduction of boric acid with sodium or magnesium. These men did not recognize the substance as an element. It was Jöns Jakob Berzelius in 1824 that identified boron as an element. The first pure boron was produced by the American chemist W. Weintraub in 1909, although this is disputed by some researchers.

Notes
At standard temperatures boron is a poor electrical conductor but is a good conductor at high temperatures.

Boron nitride can be used to make materials that are almost as hard as diamond. The nitride also acts as an electrical insulator but conducts heat similar to a metal. This element also has lubricating qualities that are similar to graphite. Boron is never found in the elemental form in nature. It was first obtained by Moissan in 1895 by reduction of boric anhydride with magnesium in a thermite-type reaction. This is still used for obtaining large quantities of impure boron. Highly purified crystalline boron is obtained by vapour phase reduction of the compound boron trichloride with hydrogen on electrically heated filaments in a flow system. The United States and Turkey are the world's largest producers of boron.

Hazards
Elemental boron and borates are not toxic and therefore do not require special precautions while handling. Some of the more exotic boron hydrogen compounds, however, are toxic as well as highly flammable and do require special handling care. Boron is highly flammable.
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Tabel Periodik

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