Patent classifications
C08J2205/042
CROSS-LINKED SBR MICROSPHERE BINDER AND PREPARATION METHOD THEREOF AND LITHIUM-ION BATTERY CONTAINING THE BINDER
A cross-linked SBR microsphere binder and a preparation method, and a lithium-ion battery containing the binder, the cross-linked SBR microsphere binder has a porous cross-linked structure, the cross-linked SBR microsphere has a particle size of 10 nm-1 μm, and a porosity of 0.01%-40%, and a pore diameter of the pore is greater than 0 and less than or equal to 200 nm. The lithium-ion battery containing the binder has advantages of better rate performance, low temperature performance, fast charge performance, and long cycle performance, compared with a lithium-ion battery containing a conventional SBR binder.
TUNABLE, RAPID UPTAKE, AMINOPOLYMER AEROGEL SORBENT FOR DIRECT AIR CAPTURE OF CO2
A porous polymer aerogel, wherein the aerogel has greater than 5 wt % of amine containing vinyl monomers integrated into a polymer backbone. A method of fabrication of a porous polymer aerogel amine material, includes preparing a solution comprising at least a solvent, amine monomers having protected amino groups, one or more crosslinkers, one or more radical initiators, and a nitroxide mediator, removing oxygen from the solution, heating the solution to promote polymerization and to produce a polymerized material, performing solvent exchange with the polymerized material, causing a deprotection reaction in the polymerized material to remove groups protecting the amino groups, soaking and rinsing the material to remove excess reagents and any byproducts of the deprotection reaction, and drying the material to produce the amine sorbent. A system to separate CO2 from other gases, comprising a polymer porous aerogel sorbent having greater than 5 wt % of amine containing vinyl monomers integrated into a polymer backbone.
Nanoporous starch aerogels impregnated with phytosterols and methods of preparing the nanoporous starch aerogels
Formation of low-crystallinity phytosterol nanoparticles via cooling-controlled supercritical carbon dioxide (SC—CO.sub.2) impregnation of phytosterols into biodegradable nanoporous starch aerogels and methods of preparing these aerogels are disclosed. The nanoporous starch aerogels increase water dissolution and bioaccessibility of the phytosterols, thereby making them available for preparation of high nutraceutical value foods.
A molding based on a monolithic organic aerogel
A molding based on a monolithic organic aerogel has a density in the range from 60 to 300 kg/m.sup.3 and a thermal conductivity in the range from 12 to 17.8 mW/m*K. The molding based on a monolithic organic aerogel has more than 30 vol.-% of pores with a diameter of less than 150 nm, and more than 20 vol.-% of pores with a diameter of less than 27 nm, based on the total pore volume. A process can be used to prepare the molding by compression.
Mesoporous organic material, useful in particular for extracting uranium(VI) from aqueous media including phosphoric acid, and uses thereof
A mesoporous organic material which makes it possible to extract, using the liquid-solid extraction technique, the uranium(VI) contained in an aqueous medium including phosphoric acid, with high efficiency and high selectivity for the iron that the medium can likewise contain. The material is likely to be obtained by cross-linking polymerisation of a monomer of formula (I) below, wherein: R.sup.1, R.sup.2 and R.sup.3 are, independently from one another, H, a C.sub.1 to C.sub.12 saturated or unsaturated, linear or branched hydrocarbon group, or a polymerisable group, with the condition that at least one of R.sup.1, R.sup.2 and R.sup.3 is a polymerisable group; R.sup.4 and R.sup.5 are, independently from one another, H or a C.sub.1 to C.sub.8 saturated or unsaturated, linear or branched hydrocarbon group; the cross-linking polymerisation being carried out in the presence of a cross-linking agent and one or more pore-forming agents.
WATER CO-CATALYST FOR POLYIMIDE PROCESSES
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.
POROUS MATERIALS FOR ENERGY MANAGEMENT
Method for preparing porous polyurethane materials with controlled pore size and shape using isocyanates, polyols, and additives, and the porous polyurethane materials prepared therefrom. Method for preparing porous polyimides using at least one polyamine and a dianhydride and the porous polyimides materials prepared therefrom. The porous materials are useful for energy management, such as thermal, impact and vibration energy, and can exhibit improved fire-resistant performance.
Fiber-reinforced organic polymer aerogel
Fiber-reinforced organic polymer aerogels, articles of manufacture and uses thereof are described. The reinforced aerogels include a fiber-reinforced organic polymer matrix having an at least bimodal pore size distribution with a first mode of pores having an average pore size of less than or equal to 50 nanometers (nm) and a second mode of pores having an average pore size of greater than 50 nm and a thermal conductivity of less than or equal to 30 mW/m.Math.K at a temperature of 20° C.
POLYURETHANE AEROGELS
The present invention relates to a method for preparing a polyurethane foam, in particular an aerogel, from at least one polyisocyanate and at least one optionally recycled polyol, and to the use thereof.
SYSTEMS AND METHODS FOR PRODUCING AEROGEL MATERIALS
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.