Patent application number | Description | Published |
20100022716 | METHOD AND FORMULA FOR FORMING HYPER-BRANCHED POLYMER - The invention provides hyper-branched polymer manufactured by adding a bismaleimide and a barbituric acid into a Brönsted base solution and reacting the mixture at 20 to 100° C. The formation may further include maleimide monomer and/or multi-maleimide monomer to modify the hyper-branched polymer properties. In addition, the barbituric acid is added to the reaction in a batch not initially charged with other reactants in a one-pot. | 01-28-2010 |
20100102265 | GEL ELECTROLYTE OF DYE SENSITIZED SOLAR CELL AND METHOD FOR MANUFACTURING THE SAME - Disclosed is a gel electrolyte for a photosensitive dye and method for manufacturing the same. First, bismaleimide and barbituric acid are dissolved in Brönsted base solution to form a gelling additive. Subsequently, the gelling additive is added into an ionic liquid electrolyte. The liquid electrolyte is then gelled at room temperature to form a gel electrolyte for the photosensitive dye utilized in dye sensitized solar cells. In addition, barbituric acid is further added into the gelling additive to enhance the gelling rate of the ionic liquid electrolyte. | 04-29-2010 |
20100130625 | PROTON EXCHANGE MEMBRANE AND METHOD FOR MANUFACTURING THE SAME - A proton exchange membrane and method for formation the same is disclosed. When forming the proton exchange membrane, first, a bismaleimide and barbituric acid are copolymerized to form a hyper-branched polymer. Next, the solvent of the sulfonated tetrafluorethylene copolymer (Nafion) aqueous solution is replaced with dimethyl acetamide (DMAc). 10 to 15 parts by weight of the hyper-branched polymer is added to 90 to 85 parts by weight of the Nafion in the DMAc solution, stood and heated to 50° C. for inter-penetration of the hyper-branched polymer and the Nafion. The heated solution is coated on a substrate, baked, and pre-treated to remove residue solvent to complete formation of the proton exchange membrane. | 05-27-2010 |
20100143767 | BINDER COMPOSITIONS AND MEMBRANE ELECTRODE ASSEMBLIES EMPLOYING THE SAME - Binder composites for membrane electrode assemblies and membrane electrode assemblies employing the same are provided. The binder composition includes a solvent, a hyper-branched polymer and a polymer with high ion conductivity, wherein the hyper-branched polymer and the polymer with high conductivity of hydronium are distributed uniformly over the solvent, and the hyper-branched polymer has a DB (degree of branching) of more than 0.5. | 06-10-2010 |
20100167101 | PROTON EXCHANGE MEMBRANE COMPOSITION - Proton exchange membrane compositions having high proton conductivity are provided. The proton exchange membrane composition includes a hyper-branched polymer, wherein the hyper-branched polymer has a DB (degree of branching) of more than 0.5. A polymer with high ion conductivity is distributed uniformly over the hyper-branched polymer, wherein the hyper-branched polymer has a weight ratio equal to or more than 5 wt %, based on the solid content of the proton exchange membrane composition. | 07-01-2010 |
20100167129 | METHOD FOR MODIFYING CATHODE MATERIAL AND LITHIUM BATTERY EMPLOYING THE CATHODE MATERIAL - The invention provides a lithium battery, including: a cathode plate and an anode plate; a separator disposed between the cathode plate and the anode plate to define a reservoir region; and an electrolyte filled in the reservoir region. A thermal protective film is provided to cover a material of the cathode plate or the anode plate. When a battery temperature rises over an onset temperature of the thermal protective film, it undergoes a crosslinking reaction to inhibit thermal runaway. A method for fabricating the lithium ion battery is also provided. | 07-01-2010 |
20130171459 | POLYAMIC ACID RESIN SOLUTION CONTAINING INTERPENETRATING POLYMER AND LAMINATE USING THE SAME - Provided is a polyamic acid resin solution containing interpenetrating polymer. The solution includes a polyamic acid resin dissolved in a solvent. The polyamic acid resin includes an interpenetrating polymer formed of polyamic acid twining around hyper-branched polybismaleimide. The hyper-branched polybismaleimide includes a bismaleimide polymer, a bismaleimide oligomer, a barbituric acid-bismaleimide copolymer or combinations thereof. | 07-04-2013 |
Patent application number | Description | Published |
20080221325 | Exchange membrane containing modified maleimide oligomers - An exchange membrane containing modified maleimide oligomers comprising sulfonated poly(aryl ether ketone) (S-PAEK) and modified maleimide oligomers. The exchange membrane uses the modified maleimide oligomers having a hyper-branched architecture as matrix, and introduces them into S-PAEK to constitute semi-interpenetration network (semi-IPN), so as to intensify water holding capacity, chemical resistance, the electrochemical stability and thermal resistance of the ionic/proton exchange membrane. The exchange membrane can be used to fabricate the membrane electrode assemblies, fuel cells, and be applied them to the fields of seawater desalination, heavy water and sewage treatment, and biomass-energy resources. | 09-11-2008 |
20100168442 | PENTAARYLDIAMINE-CONTAINING BISMALEIMIDE COMPOUND AND PRODUCING METHOD THEREOF - A pentaaryldiamine-containing bismaleimide compound of Formula (I): | 07-01-2010 |
20140175337 | Modified Maleimide Oligomer, Preparation Method Thereof and Composition Containing the Same - A modified maleimide oligomer is disclosed. The modified maleimide oligomer is made by performing a reaction of a compound having a barbituric acid structure, a free radical capture, and a compound having a maleimide structure. A composition for a battery is also disclosed. The composition includes the modified maleimide oligomer. | 06-26-2014 |
Patent application number | Description | Published |
20120153231 | CATHODE MATERIAL STRUCTURE AND METHOD FOR PREPARING THE SAME - A cathode material structure and a method for preparing the same are described. The cathode material structure includes a material body and a composite film coated thereon. The material body has a particle size of 0.1-50 μm. The composite film has a porous structure and electrical conductivity. | 06-21-2012 |
20120164511 | LITHIUM BATTERY AND ELECTRODE PLATE STRUCTURE - A lithium battery is provided. The lithium battery comprises an positive electrode plate having a first surface, a negative electrode plate having a second surface, a first thermal insulating layer and a separator. The first surface is opposite to the second surface. The thermal insulating layer is disposed on one of the first surface and the second surface. The thermal insulating layer is comprised of an inorganic material, a thermal activation material and a binder. The separator is disposed between the positive electrode plate and the negative electrode plate. | 06-28-2012 |
20120171576 | NON-AQUEOUS ELECTROLYTE AND LITHIUM SECONDARY BATTERY INCLUDING THE SAME - A non-aqueous electrolyte including a lithium salt, an organic solvent, and an electrolyte additive is provided. The electrolyte additive is a meta-stable state nitrogen-containing polymer formed by reacting Compound (A) and Compound (B). Compound (A) is a monomer having a reactive terminal functional group. Compound (B) is a heterocyclic amino aromatic derivative as an initiator. A molar ratio of Compound (A) to Compound (B) is from 10:1 to 1:10. A lithium secondary battery containing the non-aqueous electrolyte is further provided. The non-aqueous electrolyte of this disclosure has a higher decomposition voltage than a conventional non-aqueous electrolyte, such that the safety of the battery during overcharge or at high temperature caused by short-circuit current is improved. | 07-05-2012 |
20120171579 | NON-AQUEOUS ELECTROLYTE AND LITHIUM SECONDARY BATTERY INCLUDING THE SAME - A non-aqueous electrolyte including a lithium salt, an organic solvent, and an electrolyte additive is provided. The electrolyte additive is a meta-stable state nitrogen-containing polymer formed by reacting Compound (A) and Compound (B). Compound (A) is a monomer having a reactive terminal functional group. Compound (B) is a heterocyclic amino aromatic derivative as an initiator. A molar ratio of Compound (A) to Compound (B) is from 10:1 to 1:10. A lithium secondary battery containing the non-aqueous electrolyte is further provided. The non-aqueous electrolyte of this disclosure has a higher decomposition voltage than a conventional non-aqueous electrolyte, such that the safety of the battery during overcharge or at high temperature caused by short-circuit current is improved. | 07-05-2012 |
20120172558 | META-STABLE STATE NITROGEN-CONTAINING POLYMER - A meta-stable state nitrogen-containing polymer formed by reacting Compound (A) and Compound (B) is described. Compound (A) is a monomer having a reactive terminal functional group. Compound (B) is a heterocyclic amino aromatic derivative as an initiator. The molar ratio of Compound (A) to Compound (B) is from 10:1 to 1:10. The meta-stable state nitrogen-containing polymer has a variance less than 2% in its narrow molecular weight distribution after being retained at 55° C. for one month. | 07-05-2012 |
20120172593 | META-STABLE STATE NITROGEN-CONTAINING POLYMER - A meta-stable state nitrogen-containing polymer formed by reacting Compound (A) and Compound (B) is described. Compound (A) is a monomer having a reactive terminal functional group. Compound (B) is a heterocyclic amino aromatic derivative as an initiator. The molar ratio of Compound (A) to Compound (B) is from 10:1 to 1:10. The meta-stable state nitrogen-containing polymer has a variance less than 2% in its narrow molecular weight distribution after being retained at 55° C. for one month. | 07-05-2012 |
20140178751 | LITHIUM ION SECONDARY BATTERY AND ELECTROLYTE ADDITIVE FOR THE SAME - Provided is an electrolyte additive for a lithium ion secondary battery including an organic lithium compound and a hyper-branched structure material. The electrolyte additive enhances the decomposition voltage of the electrolyte up to 5.5 V, and increases the heat endurable temperature by 10° C. or more. The safety of the battery is thus improved. | 06-26-2014 |