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  2. BTX (chemistry) - Wikipedia

    en.wikipedia.org/wiki/BTX_(chemistry)

    In the petroleum refining and petrochemical industries, the initialism BTX refers to mixtures of benzene, toluene, and the three xylene isomers, all of which are aromatic hydrocarbons. The xylene isomers are distinguished by the designations ortho – (or o –), meta – (or m –), and para – (or p –) as indicated in the adjacent diagram.

  3. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    For commercial use, until World War II, much of benzene was obtained as a by-product of coke production (or "coke-oven light oil") for the steel industry. However, in the 1950s, increased demand for benzene, especially from the growing polymers industry, necessitated the production of benzene from petroleum.

  4. Linear alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Linear_alkylbenzene

    Typically, n lies between 10 and 16, although generally supplied as a tighter cut, such as C 12-C 15, C 12-C 13 and C 10-C 13, for detergent use. [1] The C n H 2n+1 chain is unbranched. They are mainly produced as intermediate in the production of surfactants, for use in detergent. Since the 1960s, LABs have emerged as the dominant precursor of ...

  5. Ethylbenzene - Wikipedia

    en.wikipedia.org/wiki/Ethylbenzene

    Ethylbenzene is an organic compound with the formula C 6 H 5 CH 2 CH 3.It is a highly flammable, colorless liquid with an odor similar to that of gasoline.This monocyclic aromatic hydrocarbon is important in the petrochemical industry as a reaction intermediate in the production of styrene, the precursor to polystyrene, a common plastic material.

  6. Raschig–Hooker process - Wikipedia

    en.wikipedia.org/wiki/Raschig–Hooker_process

    [6] [7] Due to the two step nature, the Raschig–Hooker process can be used to produce either chlorobenzene or phenol. Reaction scheme of the Raschig-Hooker process. The Raschig–Hooker process's ability to make phenol makes it comparable to other methods, such as the Dow and Bayer process, which also converts benzene into phenol. In fact ...

  7. Diethylbenzenes - Wikipedia

    en.wikipedia.org/wiki/Diethylbenzenes

    Diethylbenzenes arise as side-products of the alkylation of benzene with ethylene, which can be described as two steps. The first step is the industrial route to ethylbenzene, which is produced on a large scale as a precursor to styrene. C 6 H 6 + C 2 H 4 → C 6 H 5 C 2 H 5. The diethylbenzene is an inadvertent side product. C 6 H 5 C 2 H 5 ...

  8. Durene - Wikipedia

    en.wikipedia.org/wiki/Durene

    It is produced by methylation of other methylated benzene compounds such as p-xylene and pseudocumene. [2] C 6 H 4 (CH 3) 2 + 2 CH 3 Cl → C 6 H 2 (CH 3) 4 + 2 HCl. In industry, a mixture of xylenes and trimethylbenzenes is alkylated with methanol. Durene can be separated from its isomers by selective crystallization, exploiting its high ...

  9. Parachlorobenzotrifluoride - Wikipedia

    en.wikipedia.org/wiki/Parachlorobenzotrifluoride

    PCBTF is increasingly used as a xylene replacement in cleaners, thinners, and other aromatic hydrocarbon blends. [2] PCBTF is used as a component (5-12%) of low volatile organic compound (VOC) compliant polyurethane finishes. [5] The substance is used as an ink solvent in the printing industry. Parachlorobenzotrifluoride has a high capacity for ...