Patent classifications
C08F212/18
Anion exchange membranes and process for making
Embodiments of the present invention provide for anion exchange membranes and processes for their manufacture. The anion exchange membranes described herein are made the polymerization product of at least one functional monomer comprising a tertiary amine which is reacted with a quaternizing agent in the polymerization process.
Anion exchange membranes and process for making
Embodiments of the present invention provide for anion exchange membranes and processes for their manufacture. The anion exchange membranes described herein are made the polymerization product of at least one functional monomer comprising a tertiary amine which is reacted with a quaternizing agent in the polymerization process.
PRACTICAL SYNTHESIS OF MULTIPHASE SELF-HEALING POLYMERS FROM COMMODITY MONOMERS
A self-healing polymer material that includes a multiphase copolymer, and a method of making the copolymer, are provided. The multiphase copolymer includes one or more hydrogen bond-forming copolymer segments, each segment including a polymerized acrylamide monomer and a polymerized acrylic monomer. The polymerized acrylamide monomer includes functional groups that form hydrogen bonds in the multiphase copolymer, and is present in the one or more copolymer segments in an amount sufficient for self-healing of the multiphase copolymer.
PRACTICAL SYNTHESIS OF MULTIPHASE SELF-HEALING POLYMERS FROM COMMODITY MONOMERS
A self-healing polymer material that includes a multiphase copolymer, and a method of making the copolymer, are provided. The multiphase copolymer includes one or more hydrogen bond-forming copolymer segments, each segment including a polymerized acrylamide monomer and a polymerized acrylic monomer. The polymerized acrylamide monomer includes functional groups that form hydrogen bonds in the multiphase copolymer, and is present in the one or more copolymer segments in an amount sufficient for self-healing of the multiphase copolymer.
Cyclopropenium polymers and methods for making the same
The present invention provides, inter alia, a process for incorporating a cyclopropenium ion into a polymeric system. Processes for making cross-linked polymers, linear polymers, and dendritic polymers, as well as for incorporating a cyclopropenium ion onto a preformed polymer are also provided. Further provided are stable, polycationic compounds, various polymers that contain stable cyclopropenium cations, and substrates containing such polymers. The use of these polymers in water purification systems, antimicrobial coatings, ion-transport membranes, cell supports, drug delivery vehicles, and gene therapeutic vectors are also provided.
Cyclopropenium polymers and methods for making the same
The present invention provides, inter alia, a process for incorporating a cyclopropenium ion into a polymeric system. Processes for making cross-linked polymers, linear polymers, and dendritic polymers, as well as for incorporating a cyclopropenium ion onto a preformed polymer are also provided. Further provided are stable, polycationic compounds, various polymers that contain stable cyclopropenium cations, and substrates containing such polymers. The use of these polymers in water purification systems, antimicrobial coatings, ion-transport membranes, cell supports, drug delivery vehicles, and gene therapeutic vectors are also provided.
BLOCK COPOLYMER INTRINSIC STRETCHABLE ELECTROLUMINESCENT ELASTOMER AND PREPARATION METHOD AND APPLICATION THEREOF
The invention discloses a block copolymer intrinsic stretchable electroluminescent elastomer and its preparation method and application. This type of elastomer is made from organic electroluminescent monomers, styrene and 1,3-butadiene through anionic polymerization. The innovation of the present invention is: for the first time, the organic electroluminescence unit is introduced into the elastomer by chemical crosslinking. On the basis of improving the intrinsic stretchability of the elastomer, at the same time, it has characteristics of excellent luminescence and high carrier mobility, novel structure and unique design strategy; meanwhile, it also solves the inherent non-stretchability problem of traditional organic optoelectronic materials and the problem that traditional elastomers do not have electroluminescent properties. This type of elastomer is used as a light-emitting layer material to prepare organic electroluminescent devices with high stability, high stretchability and high efficiency.
CATIONIC COPOLYMERS WITH PENDANT N-ALLYLIMIDAZOLIUM GROUPS
Cationic copolymers having pendant N-allylimidazolium-containing groups are provided. The cationic copolymers can be used, for example, to provide anion exchange membranes for use in electrochemical cells such as fuel cells, electrolyzers, batteries, and electrodialysis cells. The anion exchange membranes typically have good mechanical properties and ionic conductivity.
CATIONIC COPOLYMERS WITH PENDANT N-ALLYLIMIDAZOLIUM GROUPS
Cationic copolymers having pendant N-allylimidazolium-containing groups are provided. The cationic copolymers can be used, for example, to provide anion exchange membranes for use in electrochemical cells such as fuel cells, electrolyzers, batteries, and electrodialysis cells. The anion exchange membranes typically have good mechanical properties and ionic conductivity.
Method to produce stimuli sensitive UV absorbing polymers
Eco-friendly aqueous synthesis of substantive, UV-absorbing, cationic polymers with ‘inverse temperature dependent solubility’ are described in the present invention. These polymers are water-soluble at ambient temperature and water-resistant at temperature of human body as well as in the presence of electrolytes. This property makes these polymers useful for personal care products that are designed for protecting skin and hair from damages of UV radiation. The invention relates to aqueous synthesis of polymers of Formula I wherein, ArCO is an UV absorbing moiety selected from 2-cyano-3,3-diphenyl acryloyl, and p-methoxy cinnamoyl, R.sub.1 is selected from H and C.sub.1-C.sub.3 alkyl group, and R.sub.2 is selected from C.sub.1-C.sub.3 alkyl group, m and n are integers and a ratio of m to n is 40:5 to 40:1. ##STR00001##