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  2. Alkoxylation - Wikipedia

    en.wikipedia.org/wiki/Alkoxylation

    PO is mainly used for alkoxylation to produce polyether polyols. The alkoxylation process is shown in simplified form: ROH + n OCH 2 CHCH 3 → R(OCH 2 CHCH 3) n OH. Polyols derived from PO have complex stereochemistry owing to the chirality of the propylene oxide.

  3. Polyol - Wikipedia

    en.wikipedia.org/wiki/Polyol

    In organic chemistry, a polyol is an organic compound containing multiple hydroxyl groups (−OH). The term "polyol" can have slightly different meanings depending on whether it is used in food science or polymer chemistry. Polyols containing two, three and four hydroxyl groups are diols, [1] triols, [2] and tetrols, [3] [4] respectively.

  4. Moisture cure polyurethane - Wikipedia

    en.wikipedia.org/wiki/Moisture_cure_polyurethane

    Moisture cured polyurethane–urea coatings have been made by reacting 1,2,3-triazole rich polyether polyols with HMDI at NCO/OH eq. ratio of 1.2 to obtain isocyanate-terminated polyurethane prepolymers. The prepolymers were cured under atmospheric moisture to make polyurethane–urea free films.

  5. Polyetheramines - Wikipedia

    en.wikipedia.org/wiki/Polyetheramines

    They are produced by reacting either ethylene oxide or propylene oxide with polyols and then aminating them. There are a number of commercially available molecules with different CAS numbers and molecular weights. They often come with a prefix of M, D or T for monofunctional, difunctional and trifunctional respectively.

  6. Ether - Wikipedia

    en.wikipedia.org/wiki/Ether

    The term polyol generally refers to polyether polyols with one or more functional end-groups such as a hydroxyl group. The term "oxide" or other terms are used for high molar mass polymer when end-groups no longer affect polymer properties. Crown ethers are cyclic polyethers.

  7. Propylene oxide - Wikipedia

    en.wikipedia.org/wiki/Propylene_oxide

    Its major application is its use for the production of polyether polyols for use in making polyurethane plastics. It is a chiral epoxide, although it is commonly used as a racemic mixture. This compound is sometimes called 1,2-propylene oxide to distinguish it from its isomer 1,3-propylene oxide, better known as oxetane.

  8. Polyisocyanurate - Wikipedia

    en.wikipedia.org/wiki/Polyisocyanurate

    The generalised chemical structure of polyisocyanurate showing the isocyanurate group. The polyols are abbreviated as R-groups.. Polyisocyanurate (/ ˌ p ɒ l ɪ ˌ aɪ s oʊ s aɪ ˈ æ nj ʊər eɪ t /), also referred to as PIR, polyol, or ISO, is a thermoset plastic [1] typically produced as a foam and used as rigid thermal insulation.

  9. Polytetrahydrofuran - Wikipedia

    en.wikipedia.org/wiki/Polytetrahydrofuran

    The material is a mixture of polyether diols terminated with alcohol groups. It is produced by polymerization of tetrahydrofuran as well as 1,4-butanediol. The product is commercially available as polymers of low average molecular weights, between 250 and 3000 daltons. In this form it is a white waxy solid that melts between 20 and 30 °C.

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