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  2. Linear alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Linear_alkylbenzene

    The DETAL process involving dehydrogenation of n-paraffins to olefins, and subsequent reaction with benzene using a fixed bed catalyst. This is newer technology and has several of the stages depicted in the HF/n-paraffins process, but it is principally different in the benzene alkylation step, during which a solid-state catalyst is employed.

  3. Mass spectral interpretation - Wikipedia

    en.wikipedia.org/wiki/Mass_spectral_interpretation

    When alkyl groups are attached to the ring, a favorable mode of cleavage is to lose a H-radical to form the tropylium cation (m/z 91). [2] [11] Benzylic cleavage. Alkyl substituted benzenes can fragment via the kinetic controlled process to form C 6 H 5 +, C 6 H 6 + ions. [11] Benzene derivatives' fragmentation process

  4. Photoionization detector - Wikipedia

    en.wikipedia.org/wiki/Photoionization_detector

    The photoionization detector was applied to gas chromatography (GC) three years later, in 1976. [5] A PID is highly selective when coupled with a chromatographic technique or a pre-treatment tube such as a benzene-specific tube. Broader cuts of selectivity for easily ionized compounds can be obtained by using a lower energy UV lamp.

  5. Electron capture detector - Wikipedia

    en.wikipedia.org/wiki/Electron_capture_detector

    The detection limit for electron capture detectors is 5 femtograms per second (fg/s) and the detector commonly exhibits a 10,000-fold linear range. [ citation needed ] This made it possible to detect halogenated compounds such as pesticides and CFCs , even at levels of only one part per trillion ( ppt ), thus revolutionizing our understanding ...

  6. Prismane - Wikipedia

    en.wikipedia.org/wiki/Prismane

    Prismane or 'Ladenburg benzene' is a polycyclic hydrocarbon with the formula C 6 H 6. It is an isomer of benzene , specifically a valence isomer . Prismane is far less stable than benzene.

  7. Liquid scintillation counting - Wikipedia

    en.wikipedia.org/wiki/Liquid_scintillation_counting

    Liquid scintillation counter. Samples are dissolved or suspended in a "cocktail" containing a solvent (historically aromatic organics such as xylene or toluene, but more recently less hazardous solvents are used), typically some form of a surfactant, and "fluors" or scintillators which produce the light measured by the detector.

  8. Benzene - Wikipedia

    en.wikipedia.org/wiki/Benzene

    Benzene is a natural constituent of petroleum and is one of the elementary petrochemicals. Due to the cyclic continuous pi bonds between the carbon atoms, benzene is classed as an aromatic hydrocarbon. Benzene is a colorless and highly flammable liquid with a sweet smell, and is partially responsible for the aroma of gasoline.

  9. Benzene (data page) - Wikipedia

    en.wikipedia.org/wiki/Benzene_(data_page)

    *** Benzene is a carcinogen (cancer-causing agent). *** Very flammable. The pure material, and any solutions containing it, constitute a fire risk. Safe handling: Benzene should NOT be used at all unless no safer alternatives are available. If benzene must be used in an experiment, it should be handled at all stages in a fume cupboard.