Disclosed is a method for producing an organic polymer aerogel and corresponding aerogels and articles of manufacture comprising such aerogels. The method can include polymerizing an organic polymerizable material in the presence of an organic solvent having a high vapor pressure and/or a low boiling point to obtain an organic polymer gel comprising an organic polymer matrix and the organic solvent, and subcritical or ambient drying the organic polymer gel under conditions suitable to remove the step (a) organic solvent and form an organic polymer aerogel.

Systems and methods for producing aerogel materials are generally described. In certain cases, the methods do not require supercritical drying as part of the manufacturing process. In some cases, certain combinations of materials, solvents, and/or processing steps may be synergistically employed so as to enable manufacture of large (e.g., meter-scale), substantially crack free, and/or mechanically strong aerogel materials.

Functionalized isocyanate based organic aerogel/xerogel/cryogel comprising: a cross-linked porous network structure made of polyurethane and/or polyisocyanurate and/or polyurea, comprising on their pore surface before functionalization reactive groups (B) and functionalization molecules having a solubility in water <10 g/L at 20 C. chemically attached to the pore surface of the cross-linked porous network structure wherein said molecules have at least one reactive group (A) being capable of binding to said pore surface (by reaction with groups (B)) and at least one functional group (C) providing the pore surface with the desired functionalization.

An aerogel that includes an open-cell structured polymer matrix that can have 5 wt. % to 50 wt. % of a polyamic amide polymer, based on the total weight of the aerogel is disclosed. The aerogel can have a density of 0.05 g/cm.sup.3 to 0.35 g/cm.sup.3 and can be thermally stable to resist browning at 330 C.

A (super)hydrophobic isocyanate based organic aerogel/xerogel/cryogel having a water contact angle of at least 90 comprising: a cross-linked porous network structure made of polyurethane and/or polyisocyanurate and/or polyurea, and hydrophobic compounds having before the gelling step at least one isocyanate-reactive group and no isocyanate groups
Characterized in that said hydrophobic compounds are covalently bonded within the porous network of the aerogel/xerogel/cryogel and wherein said bondings are created during the gelling step of the formation of the isocyanate based organic aerogel/xerogel/cryogel cross-linked porous network structure.

A macroporous-structured polymeric aerogel, and methods for making and using the same, having a polymeric matrix that includes macropores is disclosed.

Thermally treated aerogel compositions that include polyamic amides in an amount less than the aerogel compositions that include polyamic amides prior to thermal treatment, and articles of manufacture that include or are manufactured from the aerogel compositions are described.

An aerogel comprising an open-cell structured polymer matrix that includes a polyamic amide polymer is described.

A method of making an aerogel is described. The method can include obtaining a solution comprising polyamic acid and an imidazole, adding a dehydrating agent to the solution in an amount where the molar ratio of the imidazole to the dehydrating agent is 0.17:1 to 2.8:1 and reacting the solution at room temperature to 100 C. to produce a polymer matrix gel comprising a polyamic amide, and drying the polymer matrix gel to form an aerogel comprising an open-cell structured polymer matrix that includes 5 wt. % to 50 wt. % of the polyamic amide based on the total weight of the polymer aerogel.

Power generators that incorporate porous electric generation layers composed of mechanoradical-forming polymers are provided. Also provided are methods for using the generators to convert mechanical energy into and electrical signal to power electronic devices. The porous electric generation material includes an organic polymer that forms free radicals when covalent bonds are homolytically ruptured upon the application of a compressive force to the porous structure.