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  2. Initiation (chemistry) - Wikipedia

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

    In chemistry, initiation is a chemical reaction that triggers one or more secondary reactions. Initiation creates a reactive centre on a molecule which produces a chain reaction . [ 1 ] The reactive centre generated by initiation is usually a radical , but can also be cations or anions . [ 2 ]

  3. Thermophoresis - Wikipedia

    en.wikipedia.org/wiki/Thermophoresis

    When they collide with the large, slower-moving particles of the tobacco smoke they push the latter away from the rod. The force that has pushed the smoke particles away from the rod is an example of a thermophoretic force, as the mean free path of air at ambient conditions is 68 nm [2] and the characteristic length scales are between 100 ...

  4. Radical initiator - Wikipedia

    en.wikipedia.org/wiki/Radical_initiator

    For example, di-tert-butyl peroxide (t-Bu OOt-Bu) gives two t-butoxy radicals (t-BuO•) and the radicals become methyl radicals (CH 3 •) with the loss of acetone. Benzoyl peroxide (( Ph C)OO) 2 ) generates benzoyloxyl radicals (PhCOO•), each of which loses carbon dioxide to be converted into a phenyl radical (Ph•).

  5. Bulk polymerization - Wikipedia

    en.wikipedia.org/wiki/Bulk_polymerization

    The problem of heat transfer is compounded by the highly exothermic nature of free radical addition polymerization. The polymerization is obtained with a broad molecular weight distribution due to the high viscosity and lack of good heat transfer. very high molecular weights are obtained. Gel effect.

  6. Thermionic emission - Wikipedia

    en.wikipedia.org/wiki/Thermionic_emission

    For example, excited Cesium (Cs) vapors in thermionic converters form clusters of Cs-Rydberg matter which yield a decrease of collector emitting work function from 1.5 eV to 1.0–0.7 eV. Due to long-lived nature of Rydberg matter this low work function remains low which essentially increases the low-temperature converter's efficiency.

  7. Thiol-ene reaction - Wikipedia

    en.wikipedia.org/wiki/Thiol-ene_reaction

    In organosulfur chemistry, the thiol-ene reaction (also alkene hydrothiolation) is an organic reaction between a thiol (R−SH) and an alkene (R 2 C=CR 2) to form a thioether (R−S−R'). This reaction was first reported in 1905, [ 1 ] but it gained prominence in the late 1990s and early 2000s for its feasibility and wide range of applications.

  8. Autoxidation - Wikipedia

    en.wikipedia.org/wiki/Autoxidation

    It is also an important concept in both industrial chemistry and biology. [4] Autoxidation is therefore a fairly broad term and can encompass examples of photooxygenation and catalytic oxidation . The common mechanism is a free radical chain reaction , where the addition of oxygen gives rise to hydroperoxides and their associated peroxy ...

  9. List of textbooks in thermodynamics and statistical mechanics

    en.wikipedia.org/wiki/List_of_textbooks_in...

    An Introduction to Thermal Physics. United States of America: Addison Wesley Longman. ISBN 0-201-38027-7. [35] [36] [37] Blundell, Stephen; Blundell, Katherine (2006). Concepts in Thermal Physics. United Kingdom: Oxford University Press. ISBN 978-0-19-856769-1. [38] Gould, Harvey and Tobochnik, Jan (2010). Statistical and Thermal Physics ...

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