Chloride in the context of "Ammonium chloride"

Seawater, or sea water, is water from a sea or ocean. On average, seawater in the world's oceans has a salinity of about 3.5% (35 g/L, 35 ppt, 600 mM). This means that every kilogram (roughly one liter by volume) of seawater has approximately 35 grams (1.2 oz) of dissolved salts (predominantly sodium (Na) and chloride (Cl) ions). The average density at the surface is 1.025 kg/L. Seawater is denser than both fresh water and pure water (density 1.0 kg/L at 4 °C (39 °F)) because the dissolved salts increase the mass by a larger proportion than the volume. The freezing point of seawater decreases as salt concentration increases. At typical salinity, it freezes at about −2 °C (28 °F). The coldest seawater still in the liquid state ever recorded was found in 2010, in a stream under an Antarctic glacier: the measured temperature was −2.6 °C (27.3 °F).

Seawater pH is typically limited to a range between 7.5 and 8.4. However, there is no universally accepted reference pH-scale for seawater and the difference between measurements based on different reference scales may be up to 0.14 units.

Sodium chloride /ˌsoʊdiəm ˈklɔːraɪd/, commonly known as table salt, is an ionic compound with the chemical formula NaCl, representing a 1:1 ratio of sodium and chloride ions. It is transparent or translucent, brittle, hygroscopic, and occurs as the mineral halite. In its edible form, it is commonly used as a condiment and food preservative. Large quantities of sodium chloride are used in many industrial processes, and it is a major source of sodium and chlorine compounds used as feedstocks for further chemical syntheses. Another major application of sodium chloride is de-icing of roadways in sub-freezing weather.

In chemistry, a salt or ionic compound is a chemical compound consisting of an assembly of positively charged ions (cations) and negatively charged ions (anions), which results in a compound with no net electric charge. The constituent ions are held together by electrostatic forces termed ionic bonds.

The component ions in a salt can be either inorganic, such as chloride (Cl), or organic, such as acetate (CH
₃COO
). Each ion can be either monatomic, such as sodium (Na) and chloride (Cl) in sodium chloride, or polyatomic, such as ammonium (NH
₄) and carbonate (CO
₃) ions in ammonium carbonate. Salts containing basic ions hydroxide (OH) or oxide (O) are classified as bases, such as sodium hydroxide and potassium oxide.

Pitting corrosion, or pitting, is a form of extremely localized corrosion that leads to the random creation of small holes in metal. The driving power for pitting corrosion is the depassivation of a small area, which becomes anodic (oxidation reaction) while an unknown but potentially vast area becomes cathodic (reduction reaction), leading to very localized galvanic corrosion. The corrosion penetrates the mass of the metal, with a limited diffusion of ions.

Another term arises, pitting factor, which is defined as the ratio of the depth of the deepest pit (from localized corrosion) to the average penetration depth (mean thickness of the corrosion layer produced by the general uniform corrosion), which can be calculated based on the weight loss and corrosion products density.

Phosphate minerals are minerals that contain the tetrahedrally coordinated phosphate (PO3−4) anion, sometimes with arsenate (AsO3−4) and vanadate (VO3−4) substitutions, along with chloride (Cl), fluoride (F), and hydroxide (OH) anions, that also fit into the crystal structure.

The phosphate class of minerals is a large and diverse group, however, only a few species are relatively common.

Apatite is a group of phosphate minerals, usually hydroxyapatite, fluorapatite and chlorapatite, with high concentrations of OH, F and Cl ion, respectively, in the crystal. The formula of the admixture of the three most common endmembers is written as Ca₁₀(PO₄)₆(OH,F,Cl)₂, and the crystal unit cell formulae of the individual minerals are written as Ca₁₀(PO₄)₆(OH)₂, Ca₁₀(PO₄)₆F₂ and Ca₁₀(PO₄)₆Cl₂.

The mineral was named apatite by the German geologist Abraham Gottlob Werner in 1786, although the specific mineral he had described was reclassified as fluorapatite in 1860 by the German mineralogist Karl Friedrich August Rammelsberg. Apatite is often mistaken for other minerals. This tendency is reflected in the mineral's name, which is derived from the Greek word ἀπατάω (apatáō), which means to deceive.