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  2. Ethylene oxide - Wikipedia

    en.wikipedia.org/wiki/Ethylene_oxide

    Ethylene oxide scrubber: After the gaseous stream from the main reactor, containing ethylene oxide (1–2%) and CO 2 (5%), is cooled, it is then passed to the ethylene oxide scrubber. Here, water is used as the scrubbing media which scrubs away majority of ethylene oxide along with some amounts of CO 2 , N 2 , CH 2 =CH 2 , CH 4 and aldehydes ...

  3. Ethoxylation - Wikipedia

    en.wikipedia.org/wiki/Ethoxylation

    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 ...

  4. Epoxide - Wikipedia

    en.wikipedia.org/wiki/Epoxide

    For example ethylene oxide polymerizes to give polyethylene glycol, also known as polyethylene oxide. The reaction of an alcohol or a phenol with ethylene oxide, ethoxylation, is widely used to produce surfactants: [28] ROH + n C 2 H 4 O → R(OC 2 H 4) n OH. With anhydrides, epoxides give polyesters. [29]

  5. Catalytic oxidation - Wikipedia

    en.wikipedia.org/wiki/Catalytic_oxidation

    ethylene: epoxidation: mixed Ag oxides (heterogeneous) ethylene oxide: basic chemicals, surfactants cyclohexane: K-A process: Co and Mn salts (homogeneous) cyclohexanol cyclohexanone: nylon precursor ethylene: Wacker process: Pd and Cu salts (homogeneous) acetaldehyde: basic chemicals para-xylene: terephthalic acid synthesis: Mn and Co salts ...

  6. Alkoxylation - Wikipedia

    en.wikipedia.org/wiki/Alkoxylation

    Alkoxylation is a chemical reaction that involves the addition of an epoxide to another compound. 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 ...

  7. Ethylene - Wikipedia

    en.wikipedia.org/wiki/Ethylene

    In the IUPAC system, the name ethylene is reserved for the divalent group -CH 2 CH 2-. Hence, names like ethylene oxide and ethylene dibromide are permitted, but the use of the name ethylene for the two-carbon alkene is not. Nevertheless, use of the name ethylene for H 2 C=CH 2 (and propylene for H 2 C=CHCH 3) is still prevalent among chemists ...

  8. Triethanolamine - Wikipedia

    en.wikipedia.org/wiki/Triethanolamine

    Triethanolamine, or TEOA, is an organic compound with the chemical formula N(CH 2 CH 2 OH) 3. It is a colourless, viscous liquid. It is both a tertiary amine and a triol. A triol is a molecule with three alcohol groups. Approximately 150,000 tonnes were produced in 1999. [3] It is a colourless compound although samples may appear yellow because ...

  9. OMEGA process - Wikipedia

    en.wikipedia.org/wiki/OMEGA_process

    The OMEGA process ("Only MEG Advantage") [1] is a chemical process discovered by the Shell Global Solutions company that is used to produce ethylene glycol from ethylene.This process comprises two steps, the controlled oxidation of ethylene to ethylene oxide, and the net hydrolysis of ethylene oxide to monoethylene glycol (MEG). [2]