Disclosed is a low-temperature supercritical foaming process, comprising the following steps: (1) bringing a polyolefin material or a thermoplastic elastomer material into contact with at least one inert gas in a reactor at a pressure higher than atmospheric pressure to drive the gas into the material, the pressure holding temperature of the polyolefin material or thermoplastic elastomer material being lower than the melting temperature of the material by 5-40° C.; (2) reducing the pressure to expand the material so as to produce a primary foamed material, and taking out the primary foamed material; and (3) taking out the primary foamed material and putting same into a tunnel furnace for secondary foaming, the temperature of the tunnel furnace being higher than the melting temperature of the material. Compared with the prior art, the present invention features high production efficiency, energy saving, and improvement of the reactor utilization rate.

Provided is a flame-retardant foam which has high flame retardancy, is excellent in flexibility, and is excellent in stress dispersibility. Also provided is a foam member including such flame-retardant foam as a flame-retardant foam layer. The flame-retardant foam of the present invention has an apparent density of from 0.02 g/cm.sup.3 to 0.40 g/cm.sup.3, a 50% compression load of from 0.5 N/cm.sup.2 to 8.0 N/cm.sup.2, and a rupture elongation in a tensile test of 120% or less.

The present disclosure is directed to methods of forming polyimide gels. The methods generally include forming a polyamic acid and dehydrating the polyamic acid with a dehydrating agent in the presence of water. The resulting polyimide gels may be converted to polyimide or carbon xerogels or aerogels. The methods are advantageous in providing rapid or even instantaneous gelation, which may be particularly useful in formation of beads comprising the polyimide gels. Polyimide or carbon gel materials prepared according to the disclosed method are suitable for use in environments containing electrochemical reactions, for example as an electrode material within a lithium-ion battery.

The present disclosure is directed to methods of forming polyimide gels. The methods generally include forming a polyamic acid and dehydrating the polyamic acid with a dehydrating agent in the presence of water. The resulting polyimide gels may be converted to polyimide or carbon xerogels or aerogels. The methods are advantageous in providing rapid or even instantaneous gelation, which may be particularly useful in formation of beads comprising the polyimide gels. Polyimide or carbon gel materials prepared according to the disclosed method are suitable for use in environments containing electrochemical reactions, for example as an electrode material within a lithium-ion battery.

The present disclosure can provide aerogel compositions which have a thermal storage capacity, and which are durable and easy to handle. The present disclosure can provide aerogel compositions which include PCM coatings, particle mixtures, or PCM materials confined within the porous network of an aerogel composition. The present disclosure can provide methods for producing aerogel compositions by coating an aerogel composition with PCM materials, by forming particle mixtures with PCM materials, or by confining PCM materials within the porous network of an aerogel composition.

The present invention provides materials and methods for forming an interface between an appliance and living tissue using a foamed elastomeric material which contacts the tissue or similar surfaces. The elastomeric material is in the form of a durable and washable material that, when applied to or implanted in living tissue or similar surfaces, displaces and flows in to non-conforming areas creating an air and/or water tight seal that substantially returns to an original shape when removed from the contact surface. The appliance may also include structural elements designed to optimize comfort, compliance and seal achieved through minimizing the pressure variation along the contact surface of the therapy device.

A thermally insulating multilayer sheet includes a compressible layer, and a thermal insulation layer, a flame retardant layer, or a combination thereof disposed on the compressible layer.

The present disclosure provides advantageous graphene/graphite stabilized composites (e.g., graphene/graphite stabilized emulsion-templated foam composites), and improved methods for fabricating such graphene/graphite stabilized composites. More particularly, the present disclosure provides improved methods for fabricating pristine, graphene/graphite/polymer composite foams derived from emulsions stabilized by graphene/graphite kinetic trapping. In exemplary embodiments, the present disclosure provides that, instead of viewing the insolubility of pristine graphene/graphite as an obstacle to be overcome, it is utilized as a means to create or fabricate water/oil emulsions, with graphene/graphite stabilizing the spheres formed. These emulsions are then the frameworks used to make foam composites that have shown bulk conductivities up to about 2 S/m, as well as compressive moduli up to about 100 MPa and breaking strengths of over 1200 psi, with densities as low as about 0.25 g/cm.sup.3.

An object of the present invention is to provide a resin composition that can produce a foam molded body having a beautiful appearance while exhibiting excellent mechanical properties. The above object is achieved by a resin composition for producing foam particles, the resin composition comprising a base resin containing a polycarbonate resin having a glass transition temperature of 140 to 155° C. and an amorphous polyester resin having a glass transition temperature of 100 to 130° C., and the amorphous polyester containing a unit derived from a cyclic diol.

A polyolefin-based resin foamed sheet includes a polyolefin-based resin, wherein a thickness of the foamed sheet is 0.05-0.5 mm, a 25% compression hardness defined in JIS K6767(1999) is 20-100 kPa, a ratio of cell sizes in longitudinal and thickness directions is 9-30, a ratio of cell sizes in width and thickness directions is 9-30, and an average cell film thickness in the thickness direction of the foamed sheet is 2-7 μm.