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  2. Xylene - Wikipedia

    en.wikipedia.org/wiki/Xylene

    The physical properties of the isomers of xylene differ slightly. The melting point ranges from −47.87 °C (−54.17 °F) (m-xylene) to 13.26 °C (55.87 °F) (p-xylene)—as usual, the para isomer's melting point is much higher because it packs more readily in the crystal structure. The boiling point for each isomer is around 140 °C (284 °F).

  3. p-Xylene (data page) - Wikipedia

    en.wikipedia.org/wiki/P-Xylene_(data_page)

    for p-Xylene/Aniline [6] P = 745 mm Hg BP Temp. °C % by mole p-xylene liquid vapor 171: 7.5: ... data relate to Standard temperature and pressure. Reliability of ...

  4. M-Xylene (data page) - Wikipedia

    en.wikipedia.org/wiki/M-Xylene_(data_page)

    for m-Xylene/Toluene [7] P = 760 mm Hg BP Temp. °C % by mole toluene liquid vapor ... Except where noted otherwise, data relate to Standard temperature and pressure.

  5. p-Xylene - Wikipedia

    en.wikipedia.org/wiki/P-Xylene

    The p-xylene is then separated out in a series of distillation, adsorption or crystallization and reaction processes from the m-xylene, o-xylene, and ethylbenzene. Its melting point is the highest among this series of isomers, but simple crystallization does not allow easy purification due to the formation of eutectic mixtures.

  6. Poly(p-phenylene oxide) - Wikipedia

    en.wikipedia.org/wiki/Poly(p-phenylene_oxide)

    This plastic is processed by injection molding or extrusion; depending on the type, the processing temperature is 260–300 °C. The surface can be printed, hot-stamped, painted or metallized. Welds are possible by means of heating element, friction or ultrasonic welding. It can be glued with halogenated solvents or various adhesives.

  7. Terephthalic acid - Wikipedia

    en.wikipedia.org/wiki/Terephthalic_acid

    Terephthalic acid was produced by oxidation of p-xylene with 30-40% nitric acid. Air oxidation of p-xylene gives p-toluic acid, which resists further air-oxidation. Esterification of p-toluic acid to methyl p-toluate (CH 3 C 6 H 4 CO 2 CH 3) opens the way for further oxidation to monomethyl terephthalate. In the Dynamit−Nobel process these ...

  8. Parylene - Wikipedia

    en.wikipedia.org/wiki/Parylene

    Parylene was discovered in 1947 by Michael Szwarc as one of the thermal decomposition products of para-xylene H 3 C − C 6 H 4 − CH 3 above 1000 °C. Szwarc identified para-xylylene as the precursor by observing that reaction with iodine yielded para-xylylene di-iodide as the only product.

  9. Polyethylene - Wikipedia

    en.wikipedia.org/wiki/Polyethylene

    The melting point for average commercial low-density polyethylene is typically 105 to 115 °C (221 to 239 °F). These temperatures vary strongly with the type of polyethylene, but the theoretical upper limit of melting of polyethylene is reported to be 144 to 146 °C (291 to 295 °F). Combustion typically occurs above 349 °C (660 °F).