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  2. Polystyrene - Wikipedia

    en.wikipedia.org/wiki/Polystyrene

    Expanded polystyrene packaging A polystyrene yogurt container Bottom of a vacuum-formed cup; fine details such as the glass and fork food contact materials symbol and the resin identification code symbol are easily molded. Polystyrene (PS) / ˌ p ɒ l i ˈ s t aɪ r iː n / is a synthetic polymer made from monomers of the aromatic hydrocarbon ...

  3. Epoxidized soybean oil - Wikipedia

    en.wikipedia.org/wiki/Epoxidized_soybean_oil

    Epoxidized linolein, a major component of ESBO.. ESBO is manufactured from soybean oil through the process of epoxidation.Polyunsaturated vegetable oils are widely used as precursors to epoxidized oil products because they have high numbers of carbon-carbon double bonds available for epoxidation. [4]

  4. Polystyrene sulfonate - Wikipedia

    en.wikipedia.org/wiki/Polystyrene_sulfonate

    Polystyrene sulfonic acid, the acid whose salts are the polystyrene sulfonates, has the idealized formula (CH 2 CHC 6 H 4 SO 3 H) n. The material is prepared by sulfonation of polystyrene: (CH 2 CHC 6 H 5) n + n SO 3 → (CH 2 CHC 6 H 4 SO 3 H) n. Several methods exist for this conversion, which can lead to varying degree of sulfonation.

  5. Natural oil polyols - Wikipedia

    en.wikipedia.org/wiki/Natural_oil_polyols

    The structure below shows the major component of castor oil which is composed of the tri-ester of rincinoleic acid and glycerin: Major component of castor oil Other vegetable oils - such as soy bean oil, [ 3 ] peanut oil , and canola oil - contain carbon-carbon double bonds, but no hydroxyl groups.

  6. Styrene maleic anhydride - Wikipedia

    en.wikipedia.org/wiki/Styrene_maleic_anhydride

    Styrene maleic anhydride (SMA or SMAnh) is a synthetic polymer that is built-up of styrene and maleic anhydride monomers.In one copolymer, the monomers can be almost perfectly alternating.

  7. α-Methylstyrene - Wikipedia

    en.wikipedia.org/wiki/Α-Methylstyrene

    AMS is formed as a by-product of the cumene process.In this procedure, cumene is converted to its radical, through a reaction with oxygen. Normally these cumene radicals are converted to cumene hydroperoxide, however they can also undergo radical disproportionation to form AMS.

  8. Thioester - Wikipedia

    en.wikipedia.org/wiki/Thioester

    In a thionoester, sulfur replaces the carbonyl oxygen in an ester. Methyl thionobenzoate is C 6 H 5 C(S)OCH 3. Such compounds are typically prepared by the reaction of the thioacyl chloride with an alcohol. [16] They can also be made by the reaction of Lawesson's reagent with esters or by treating pinner salts with hydrogen sulfide.

  9. Styrene-acrylonitrile resin - Wikipedia

    en.wikipedia.org/wiki/Styrene-acrylonitrile_resin

    It is widely used in place of polystyrene owing to its greater thermal resistance. The chains of between 70 and 80% by weight styrene and 20 to 30% acrylonitrile. [ 1 ] Larger acrylonitrile content improves mechanical properties and chemical resistance, but also adds a yellow tint to the normally transparent plastic.