Aliphatic polyimides from a 1:2 molar ration of diamine and unsaturated monoanhydride or unsaturated diacid
Aliphatic polyimides are synthesized by a 2:1 molar ratio reaction of an unsaturated monoanhydride or an unsaturated diacid with a diamine. Bio-derived monomers are particularly useful in the synthesis of the aliphatic polyimides.
1. An aliphatic polyimide, wherein the aliphatic polyimide is poly-3,3′,4,4′-yl-((1,1′-bis trimethylene-poly dimethyl siloxane-1,ω-diyl)-bis-(3-methyl-pyrrolidine-2,5-dione)).
2. The aliphatic polyimide of claim 1 ,
wherein the polyimide is formed by the reaction of a monoanhydride to a diamine at a 2:1 molar ratio, giving a ring-opened amic acid, followed by self-polymerization at a temperature of about 220° C. to form the aliphatic polyimide, wherein the monohydride is citraconic anhydride.
3. An aliphatic polyimide which is a reaction product of a 2:1 molar ratio of an unsaturated monoanhydride with a diamine, wherein the diamine is aminopropyl terminated polydimethyl siloxane and wherein the unsaturated monoanhydride is citraconic anhydride.
4. A compound comprising the aliphatic polyimide of claim 1 and one or more functional additives.
5. The compound of claim 4 , wherein the functional additive is selected from the group consisting of adhesion promoters; biocides; anti-fogging agents; anti-static agents; bonding, blowing and foaming agents; dispersants; fillers, fibers, and extenders; flame retardants; smoke suppressants; impact modifiers; initiators; lubricants; micas; pigments, colorants and dyes; plasticizers; processing aids; release agents; silanes, titanates and zirconates; slip and anti-blocking agents; stabilizers; stearates; ultraviolet light absorbers; viscosity regulators; waxes; catalyst deactivators, and combinations of them.