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Bromine itself can be used, but due to its toxicity and volatility, safer brominating reagents are normally used, such as N-bromosuccinimide. The principal reactions for organobromides include dehydrobromination , Grignard reactions , reductive coupling , and nucleophilic substitution .
Paradox of the pesticides; Paraquat; Paris Green; Pendimethalin; Pentachloronitrobenzene; Pentachlorophenol; Permethrin; Persistent organic pollutant; Pest control
The first bromine extraction plant in Arkansas opened in 1957. [7] By 1969, five companies were operating plants there. For most of the 20th century, the principal use of bromine was as the gasoline additive ethylene dibromide, which was needed in leaded gasoline to prevent lead deposits in car engines.
The major sources include sea spray, salt lakes, marshes, volcanos, anthropogenic sources, and the least input is the polar regions. Bromine's chemistry is linked to other halogens such as chlorine and iodine amplify atmospheric cycling that contributes to troposphere and stratosphere ozone layer destruction.
Bronopol is used in consumer products as an effective preservative agent, as well as a wide variety of industrial applications (almost any industrial water system is a potential environment for bacterial growth, leading to slime and corrosion problems - in many of these systems bronopol can be a highly effective treatment).
Silver bromide (AgBr). Nearly all elements in the periodic table form binary bromides. The exceptions are decidedly in the minority and stem in each case from one of three causes: extreme inertness and reluctance to participate in chemical reactions (the noble gases, with the exception of xenon in the very unstable XeBr 2; extreme nuclear instability hampering chemical investigation before ...
Where desired, free bromine may be obtained by thermal decomposition of ferrous bromide. [1] Before Dow entered the bromine business, brine was evaporated by heating with wood scraps and then crystallized sodium chloride was removed. An oxidizing agent was added, and bromine was formed in the solution. Then bromine was distilled.
Another equation that can be applied to get the correct molecular formula of the CFC/R/Freon class compounds is to take the numbering and add 90 to it. The resulting value will give the number of carbons as the first numeral, the second numeral gives the number of hydrogen atoms, and the third numeral gives the number of fluorine atoms.