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In organic chemistry, ethoxylation is a chemical reaction in which ethylene oxide (C 2 H 4 O) adds to a substrate. It is the most widely practiced alkoxylation, which involves the addition of epoxides to substrates. In the usual application, alcohols and phenols are converted into R(OC 2 H 4) n OH, where n ranges from 1 to 10. Such compounds ...
It is a popular solvent for commercial applications. [1] It is produced by the ethoxylation of ethanol (CH 3 CH 2 OH). Applications ... Toggle the table of contents ...
It is formed by the ethoxylation chemical reaction of dodecanol (lauryl alcohol) to give a material with 5 repeat units of ethylene glycol. Multilamellar vesicle formation [ edit ]
The usual manifestation of this reaction is ethoxylation of alcohols (ROH), in which case ethylene oxide is the alkoxylating agent: ROH + C 2 H 4 O → ROCH 2 CH 2 OH. Another industrially significant epoxide is propylene oxide (PO, OCH 2 CHCH 3). PO is mainly used for alkoxylation to produce polyether polyols.
Narrow-range ethoxylates (NREs) in chemistry are fatty alcohol polyglycol ethers with a narrow homolog distribution and are known nonionic surfactants.They can be produced industrially, for example, by the addition of ethylene oxide onto fatty alcohols in the presence of suitable catalysts (layer compounds which have been calcined or hydrophobized with fatty acids).
Nonoxynols are produced by ethoxylation of alkylphenols and vary in the number of repeating ethoxy (oxy-1,2-ethanediyl) groups resulting in Nonoxynol-4, Nonoxynol-7, Nonoxynol-9, Nonoxynol-14, Nonoxynol-15, Nonoxynol-18, Nonoxynol-40, Nonoxynol-30 and Nonoxynol-50. Other synonyms are polyethylene glycol (PEG)-7 Nonyl phenyl ether, PEG-14 Nonyl ...
It is therefore sometimes used in epoxy chemistry enabling a large reduction in cure time. [5] As the molecule has 4 functional acrylate groups it confers high cross-link density. Ethoxylation maybe used to produce ethoxylated versions which find use in electron beam curing. [6] The material also has pharmaceutical uses [7]
It can be shown that the impurity profile of the mother liquors, at moderate recycle levels (i.e. when x>1), quickly reaches a steady state according to (1 − x n +1)/(1 − x), where n is the number of times the process is operated and x is the fraction of mother liquors recycled (Fig. 1). [3]