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395 results about "Composite matrix" patented technology

Method to prepare processable polyimides with reactive endogroups using 1,3-bis(3-aminophenoxy)benzene

InactiveUS6288209B1Improved solvent resistance and modulus and elevated use temperatureImproved melt processabilityNon-fibrous pulp additionSynthetic resin layered productsPolymer scienceBackbone chain
Polyimide copolymers were obtained containing 1,3-bis(3-aminophenoxy)benzene (APB) and other diamines and dianhydrides and terminating with the appropriate amount of reactive endcapper. The reactive endcappers studied include but should not be limited to 4-phenylethynyl phthalic anhydride (PEPA), 3-aminophenoxy-4'-phenylethynylbenzophenone (3-APEB), maleic anhydride (MA) and nadic anhydride (5-norbornene-2,3-dicarboxylic anhydride, NA). Homopolymers containing only other diamines and dianhydrides which are not processable under conditions described previously can be made processable by incorporating various amounts of APB, depending on the chemical structures of the diamines and dianhydrides used. By simply changing the ratio of APB to the other diamine in the polyimide backbone, a material with a unique combination of solubility, Tg, Tm, melt viscosity, toughness and elevated temperature mechanical properties can be prepared. The copolymers that result from using APB to enhance processability have a unique combination of properties that include low pressure processing (200 psi and below), long term melt stability (several hours at 300° C. for the phenylethynyl terminated polymers), high toughness, improved solvent resistance, improved adhesive properties, and improved composite mechanical properties. These copolyimides are eminently suitable as adhesives, composite matrices, moldings, films and coatings.
Owner:NASA

Method to prepare processable polyimides with reactive endgroups using 1,3-bis (3-aminophenoxy) benzene

Polyimide copolymers were obtained containing 1,3-bis(3-aminophenoxy)benzene (APB) and other diamines and dianhydrides and terminating with the appropriate amount of reactive endcapper. The reactive endcappers studied include but should not be limited to 4-phenylethynyl phthalic anhydride (PEPA), 3-aminophenoxy-4'-phenylethynylbenzophenone (3-APEB), maleic anhydride (MA) and nadic anhydride (5-norbornene-2,3-dicarboxylic anhydride, NA). Homopolymers containing only other diamines and dianhydrides which are not processable under conditions described previously can be made processable by incorporating various amounts of APB, depending on the chemical structures of the diamines and dianhydrides used. By simply changing the ratio of APB to the other diamine in the polyimide backbone, a material with a unique combination of solubility, Tg, Tm, melt viscosity, toughness and elevated temperature mechanical properties can be prepared. The copolymers that result from using APB to enhance processability have a unique combination of properties that include low pressure processing (200 psi and below), long term melt stability (several hours at 300 DEG C. for the phenylethynyl terminated polymers), high toughness, improved solvent resistance, improved adhesive properties, and improved composite mechanical properties. These copolyimides are eminently suitable as adhesives, composite matrices, moldings, films and coatings.
Owner:NAT AERONAUTICS & SPACE ADMINSTRATION NASA THE

Ambient temperature rapid self-polymerization compositions of high cross-linked or linear type beta-amino-ester alternative co-polymers and their applications

InactiveUS20070299211A1Self-polymerization can be very rapidSelf-polymerization rate can be controlledCross-linkAmino esters
Self-polymerization of mono-aziridine (or azetidine) and multi-aziridine (or azetidine) containing compounds with vinyl group containing organic acid, such as acrylic acid (AA), 2-methylenesuccinic acid, 2,3-dimethylenesuccinic acid and etc, at ambient temperature results in the new type of cross-linked and linear type copolymers, respectively.
The polymerization of multi-functional aziridine (or azetidine) containing compounds with vinyl group containing organic acid results in the formation of high cross-linked polymers. The self-polymerization takes place at ambient temperature and the resultants, cross-linked polymeric networked materials, are solvent insoluble and potential for adhesive, composite matrix and other applications. These insoluble materials are hydrolyzed in an acidic or basic condition to form the water soluble β-amino acids.
A linear poly(β-aminoester) is obtained from the self-polymerization of vinyl group containing organic acid with mono-aziridine (or azetidine) containing compound at ambient temperature. poly(β-aminoester) is applicable for gene transfer, controlled drug release and other applications. This self-polymerization process offers a convenient route for preparing poly(β-aminoesters).
Owner:TAMKANG UNIVERSITY

Electromagnetic shielding composite material

The invention discloses an electromagnetic shielding composite material. Electromagnetic wave absorption layers and electromagnetic wave reflection layers are alternately overlapped to form electromagnetic shielding function bodies; the electromagnetic wave absorption layers are formed by compositing matrix resin, fiber carriers and electromagnetic absorption function bodies; the electromagnetic wave absorption layers are formed by compositing matrix resin and electromagnetic gradient reflection function bodies; in the overlapped electromagnetic wave reflection layers, the mass percentage compositions of short cut carbon fibers increase in gradient along the incident directions of the electromagnetic waves. According to the electromagnetic shielding composite material of the invention, the incident electromagnetic waves generate multi-reflection; the propagation paths of the electromagnetic waves in the material are increased; increase of the multi-reflection loss and absorption loss enables the shielding efficiency of the material to be increased; in adoption of the reflection layers of gradient structure, the electromagnetic waves will not escape away from the shielding material rapidly for reflection; more electromagnetic waves can enter the next shielding unit; therefore, the shielding efficiency of the material is further improved.
Owner:WUHAN UNIV OF TECH
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