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Polyethylene absorbs almost no water; the gas and water vapour permeability (only polar gases) is lower than for most plastics. Oxygen, carbon dioxide and flavorings, on the other hand, can pass it easily. Polyethylene burns slowly with a blue flame having a yellow tip and gives off an odour of paraffin (similar to candle flame). The material ...
One of the main environmental benefits of Green PE is the sequestration of roughly 2.15 tonnes of CO 2 per tonne of Green Polyethylene produced, which comes from the CO 2 absorbed by the sugar cane while growing, minus the CO 2 emitted through the production process. Renewable polyethylene is non-biodegradable and can be recycled in the same ...
All organisms produce alcohol in small amounts by several pathways, primarily through fatty acid synthesis, [70] glycerolipid metabolism, [71] and bile acid biosynthesis pathways. [72] Fermentation is a biochemical process during which yeast and certain bacteria convert sugars to ethanol, carbon dioxide, as well as other metabolic byproducts.
Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula C 2 H 4 or H 2 C=CH 2.It is a colourless, flammable gas with a faint "sweet and musky" odour when pure. [7] It is the simplest alkene (a hydrocarbon with carbon–carbon double bonds).
The name of each polyolefin indicates the olefin from which it is prepared; for example, polyethylene is derived from ethylene, and polymethylpentene is derived from 4-methyl-1-pentene. Polyolefins are not olefins themselves because the double bond of each olefin monomer is opened in order to form the polymer.
In a similar way, the Phillips slurry process uses silica-based catalysts in contact with a fast-moving hydrocarbon and polyethylene slurry to precipitate high density polyethylene. [18] Processing will determine the properties of the HDPE. The method used to synthesize the HDPE is crucial because the micro structure of the HDPE will vary.
In the production process, two-thirds of the triethylaluminium produced is recycled back into the reactor, and only one-third is used to produce the fatty alcohols. The recycling step is used to produce triethylaluminium at a higher yield and with less time. Triethylaluminium reacts with ethylene to form higher molecular weight trialkylaluminium.
The industrial synthesis of acetaldehyde (Wacker process) proceeds via the intermediacy of a vinyl alcohol complex. [ 4 ] The uncatalyzed keto–enol tautomerism by a 1,3-hydrogen migration is forbidden by the Woodward–Hoffmann rules and therefore has a high activation barrier and is not a significant pathway at or near room temperature.