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The Boron name was used outside of Ohio in neighboring states, like Michigan, Pennsylvania, Kentucky and West Virginia. Boron was also the branding of its premium grade gasoline along with its regular grade fuel "Extron" (formerly "Ex-tane" later "Octron") and its unleaded version "Cetron" introduced in 1970. [citation needed]
Trimethylborane spontaneously ignites in air if the concentration is high enough. It burns with a green flame producing soot. [11] Slower oxidation with oxygen in a solvent or in the gas phase can produce dimethyltrioxadiboralane, which contains a ring of two boron and three oxygen atoms.
Triethylborane is strongly pyrophoric, with an autoignition temperature of −20 °C (−4 °F), [13] burning with an apple-green flame characteristic for boron compounds. Thus, it is typically handled and stored using air-free techniques .
Gasoline + Oxygen –> Derived from Gasoline: 13.3 [citation needed] Dinitroacetylene explosive - computed [citation needed] 9.8: Octanitrocubane explosive: 8.5 [6] 16.9 [7] Tetranitrotetrahedrane explosive - computed [citation needed] 8.3: Heptanitrocubane explosive - computed [citation needed] 8.2: Sodium (reacted with chlorine) [citation ...
In general terms, boron-enhanced fuels offer up to 40% higher energy density than plain JP-4 in terms of both weight and volume. [ 3 ] [ 4 ] In the US a whole family of fuels were investigated, and generally referred to by the names they were assigned during the Air Force's Project HEF: HEF-1 (ethyldiborane), HEF-2 (propylpentaborane), HEF-3 ...
Ammonia borane has been suggested as a storage medium for hydrogen, e.g. for when the gas is used to fuel motor vehicles. It can be made to release hydrogen on heating, being polymerized first to (NH 2 BH 2) n, then to (NHBH) n, [15] which ultimately decomposes to boron nitride (BN) at temperatures above 1000 °C. [16]
Boron-boron multiple bonds are rare, although doubly-bonded dianions have been known since the 1990s. [20] Neutral analogues use NHC adducts, such as the following diborane(2) derivative: [21] [22] Each boron atom has an attached proton and is coordinated to a NHC carbene. [23] [24] A reported diboryne is based on similar chemistry. [25]
Trimethyl borate is the main precursor to sodium borohydride by its reaction with sodium hydride in the Brown-Schlesinger process: . 4 NaH + B(OCH 3) 3 → NaBH 4 + 3 NaOCH 3. It is a gaseous anti-oxidant in brazing and solder flux.