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Borate ions occur, alone or with other anions, in many borate and borosilicate minerals such as borax, boracite, ulexite (boronatrocalcite) and colemanite. Borates also occur in seawater, where they make an important contribution to the absorption of low frequency sound in seawater. [1] Borates also occur in plants, including almost all fruits. [2]
So do your best to plant deer-resistant types of plants and protect your favorites with a natural barrier. Then try repellent as an additional measure, and hope for the best.
Borax as a source of borate has been used to take advantage of the co-complexing ability of borate with other agents in water to form complex ions with various substances. Borate and a suitable polymer bed are used to chromatograph non- glycated hemoglobin differentially from glycated hemoglobin (chiefly HbA1c ), which is an indicator of long ...
In halogen-free system, zinc borate can be used together with alumina trihydrate, magnesium hydroxide, red phosphorus, or ammonium polyphosphate. During burning the plastics, a porous borate ceramics is formed that protects the underlying layers. In presence of silica, borosilicate glass can be formed at plastic burning temperatures. [4]
The Borate Minerals are minerals which contain a borate anion group. The borate (BO 3) units may be polymerised similar to the SiO 4 unit of the silicate mineral class. This results in B 2 O 5, B 3 O 6, B 2 O 4 anions as well as more complex structures which include hydroxide or halogen anions. [2] The [B(O,OH) 4] − anion exists as well.
A member of this family is called a deer or a cervid. They are widespread throughout North and South America, Europe, and Asia, and are found in a wide variety of biomes . Cervids range in size from the 60 cm (24 in) long and 32 cm (13 in) tall pudú to the 3.4 m (11.2 ft) long and 3.4 m (11.2 ft) tall moose .
Borate buffered saline (abbreviated BBS) is a buffer used in some biochemical techniques to maintain the pH within a relatively narrow range. Borate buffers have an alkaline buffering capacity in the 8–10 range.
Trimethyl borate is a popular borate ester used in organic synthesis. Borate esters form spontaneously when treated with diols such as sugars and the reaction with mannitol forms the basis of a titrimetric analytical method for boric acid. Metaborate esters show considerable Lewis acidity and can initiate epoxide polymerization reactions. [4]