Disclosed are cellulose-based flexible gels containing cellulose nanorods, ribbons, fibers, and the like, and cellulose-enabled inorganic or polymeric composites, wherein the gels have tunable optical, heat transfer, and stiffness properties. The disclosed gels are in the form of hydrogels, organogels, liquid-crystal (LC) gels, and aerogels, depending on the solvents in the gels.

Bare porous polymer monoliths, fluidic chips, methods of incorporating bare porous polymer monoliths into fluidic chips, and methods for functionalizing bare porous polymer monoliths are described. Bare porous polymer monoliths may be fabricated ex situ in a mold. The bare porous polymer monoliths may also be functionalized ex situ. Incorporating the bare preformed porous polymer monoliths into the fluidic chips may include inserting the monoliths into channels of channel substrates of the fluidic chips. Incorporating the bare preformed porous polymer monoliths into the fluidic chips may include bonding a capping layer to the channel substrate. The bare porous polymer monoliths may be mechanically anchored to channel walls and to the capping layer. The bare porous polymer monoliths may be functionalized by ex situ immobilization of capture probes on the monoliths. The monoliths may be functionalized by direct attachment of chitosan.

An organic polymer aerogel that includes an organic polymer gel matrix and microstructures dispersed or embedded within the aerogel is disclosed. The aerogel can have an at least bimodal pore size distribution comprising a first peak of less than or equal to 65 nm and a second peak greater than or equal to 100 nm.

Mechanically strong, biodegradable and reusable aerogels are disclosed, which can be made with a cross-linked cellulose ester, and which exhibit a low density and high porosity. The aerogels disclosed herein may be used as sorbent materials and can be modified with a hydrophobic and/or oleophilic agent.

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 method produces porous materials by expansion of polymer gels. The porous materials can be a micro- or nano-porous polymer materials.

A process for preparing a porous material involves at least the steps of providing a mixture (I) containing a composition (A), which contains components suitable to from an organic gel, and a solvent (B); reacting the components in the composition (A) in the presence of the solvent (B) to form a gel; and drying of the gel. The composition (A) contains a catalyst system (CS), which contains at least a catalyst component (C1) selected from ammonium salts and phosphonium salts, and an acid with a phosphor containing acid group as a catalyst component (C2). Porous materials can be obtained in this way and the porous materials can be used as thermal insulation material and in vacuum insulation panels and vacuum insulation systems, in particular in interior or exterior thermal insulation systems as well as for insulation of refrigerators and freezers and in water tank or ice maker insulation systems.

An organic polymer aerogel that includes an organic polymer gel matrix and microstructures dispersed or embedded within the aerogel is disclosed. The aerogel can have an at least bimodal pore size distribution comprising a first peak of less than or equal to 65 nm and a second peak greater than or equal to 100 nm.

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.

A wet gel granule of aerogel is prepared by the following steps: mixing step: mixing with an organic mixed solvent to form a mixed solution; hydrolysis step: adding an acid catalyst to the mixed solution for carrying out a hydrolysis reaction, and adding a dispersion solvent during the condensation reaction, and agitating to gel the mixed solution during agitation and produce multiple hydrophilic or hydrophobic wet gel granules of aerogel. The overall preparation speed can be shortened quickly and at the same time the hydrophilic or hydrophobic wet gel granules of aerogel wet glue particles are prepared to increase the production efficiency of the wet gel granules of aerogel.