US2023265235A1PendingUtilityA1

Curable polyfarnesene-based compositions

87
Assignee: FINA TECHNOLOGYPriority: Jan 6, 2016Filed: Mar 22, 2023Published: Aug 24, 2023
Est. expiryJan 6, 2036(~9.5 yrs left)· nominal 20-yr term from priority
C08F 236/22C08C 19/20C08C 19/22C08F 236/06C08G 18/10C08G 18/69C08F 2810/40C08G 2190/00C08F 8/32C08F 36/22C08G 18/6204C08F 8/04C08F 8/08C08F 8/14C08G 18/12C08G 18/3206C08G 18/6588C08G 18/6208C08G 18/7671C08G 18/698C08F 136/22C09D 175/14C09J 175/14C09K 3/1021C08L 47/00C08F 236/10C08G 2101/00C08G 2150/00C08G 2170/00C09D 13/00
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Claims

Abstract

A polymer having a hydrophobic polymer chain derived from monomers of farnesene and other optional monomers, such as dienes and vinyl aromatics. The polymer also includes one or more terminal functional groups, such as an amino group, a glycidyl group, a carboxylic acid group, a (meth)acrylate group, a silane group, an isocyanate group, an acetoacetate group, a phenolic group, and a hydroxyl group. Functional groups, such as carboxylic acids, may also be grafted along the hydrophobic polymer chain. The polymer may be incorporated in curable compositions that optionally include one or more polymer resins having similar functional groups. Methods for preparing the curable polymer compositions are also provided. The curable or cured form of the polymer composition may be used in various products, such as a sealant, a coating, a caulk, an electric potting compound, a membrane, a sponge, a foam, an adhesive, or a propellant binder.

Claims

exact text as granted — not AI-modified
1 - 57 . (canceled) 
     
     
         58 . A method of preparing a polymer, wherein the polymer comprises a hydrophobic polymer chain derived from at least one monomer comprising farnesene, at least one terminal functional group, and an amine-terminated polyfarnesene and the method comprises:
 reacting one or more polyols comprising a polyfarnesene polyol with at least one of an alkanesulfonyl chloride, an alkanesulfonyl fluoride, an arenesulfonyl chloride, and an arenesulfonyl fluoride in the presence of a tertiary amine catalyst to form at least one of an alkanesulfonate and arenesulfonate terminated polymer; and   reacting the alkanesulfonate or arenesulfonate terminated polymer with a primary amine or ammonia to provide the amine-terminated polyfarnesene.

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