The present invention relates to a process for the preparation of Sevelamer carbonate from polyallylamine hydrochloride.

The present application is directed to methods for preparation of polymer particles in gel form and carbon materials made therefrom. The carbon materials comprise enhanced electrochemical properties and find utility in any number of electrical devices, for example, as electrode material in ultracapacitors or batteries. The methods herein can also be employed generally to improve emulsion and/or suspension polymerization processes by improved control of diffusion of acidic and basic species between the polymer and secondary phases.

The present invention relates to a composition for a gel polymer electrolyte comprising a liquid electrolyte solvent, a lithium salt, a polymerization initiator, and a mixed compound of a first compound and a second compound, and a lithium secondary battery comprising a positive electrode, a negative electrode, a separator, and a gel polymer electrolyte, wherein the gel polymer electrolyte is formed by polymerizing the composition for a gel polymer electrolyte. By comprising a mixed compound of a first compound and a second compound in which the first compound is an amine-based compound comprising polyethylene glycol as a functional group and the second compound is an epoxy-based compound, a composition for a gel polymer electrolyte of the present invention exhibits, when used in a lithium secondary battery, enhanced battery lifespan, excellent high temperature storability, and enhanced battery capacity property by readily inducing a hopping phenomenon.

Matrix materials, such as sol-gels and polymers derivatives to contain a redox active material can be used to form electrodes and probes suitable for use in pH meters and other analyte sensing devices.

The present invention relates to polymers having dynamic urea bonds and more specifically to polymers having hindered urea bonds (HUBs) with fast hydrolytic kinetics. These urea bonds are aryl-substituted, i.e. aromatic-substituted hindered urea bonds, that demonstrate pH independent hydrolytic kinetics, such that they consistently and rapidly hydrolyze in water from pH 2 to 11. The urea bond dissociation for these materials is generally such that k.sub.1>h.sup.1, which is two orders of magnitudes faster than for aliphatic hindered ureas. The present invention also relates to hydrolytically reversible or degradable linear, branched or network polymers incorporating these HUBs and to precursors for incorporation of these HUBs into these polymers. The technology can be applied to and integrated into a variety of polymers, such as polyureas, polyurethanes, polyesters, polyamides, polycarbonates, polyamines, and polysaccharides to make linear, branched, and cross-linked polymers. Polymers incorporating these HUBs can be used in a wide variety of applications including for example, environmentally compatible packaging materials and biomedical applications, such as drug delivery systems and tissue engineering. In other embodiments, the HUBs can be used in self-healing polymers.

Ionic liquid N-methyl-N-propyl-pyrrolidinium bis(fluorosulfonyl)imide (Pyr.sub.13FSI) was introduced into a hybrid network to obtain a series of gel polymer electrolytes (GPEs). Mechanical and electrochemical properties of the GPEs were tuned through controlling the network structure and ionic liquid contents, and ionic conductivity higher than 1 mS cm.sup.?1 at room temperature was achieved. The newly developed GPEs are flame-retardant and show excellent thermal and electrochemical stability as well as ultra-stability with lithium metal anode. Symmetrical lithium cells with the GPEs exhibit a stable cycling over 6800 h at a current density of 0.1 mA cm.sup.?2 and stable lithium stripping-plating at 1 mA cm.sup.?2, the highest current density reported for ionic liquid-based GPEs. Moreover, Li/LiFePO.sub.4 batteries with the obtained GPEs exhibit desirable cycling stability and rate performance over a wide temperature range from 0? C. to 90? C.

The present invention provides a sustained release composition having hyperbranched polymers that are polyesters that are biobased and biodegradable, and that have at least one active ingredient, which composition delivers the active ingredient over time. These active ingredients can be a wide variety of compounds so long as they can covalently bind to the polymer or be encapsulated in the polymer in a manner that is released at the point of delivery, usually by acid hydrolysis or enzymatic bond scission.

The present invention relates to biostable gel comprising: (a) at least one silicon-containing polyol, polyamine, polyepoxy or polyisocyanate having 1 or more functional groups and a molecular weight of at least 20,000 which is cured in the presence of: (b) at least one diol, diamine or diisocyanate having a molecular weight of less than 10,000; and/or (c) an initiator,
processes for their preparation and their use in the manufacture and repair of biomaterials and medical devices, articles or implants, in particular the manufacture of a soft tissue implant such as breast implants and the repair of orthopaedic joints such as spinal discs.

Polyimide-network battery-separator compositions are disclosed. The polyimide-network battery-separator compositions comprise a porous cross-linked polyimide network comprising a polyamic acid oligomer. The polyamic acid oligomer (i) comprises a repeating unit of a dianhydride and a diamine and terminal functional groups, (ii) has an average degree of polymerization of 10 to 70, (iii) has been cross-linked via a cross-linking agent, comprising three or more cross-linking groups, at a balanced stoichiometry of the cross-linking groups to the terminal functional groups, and (iv) has been chemically imidized to yield the porous cross-linked polyimide network. The polyimide-network battery-separator compositions also comprise an electrolyte composition comprising (i) a room temperature ionic liquid and (ii) a lithium ion. The electrolyte composition is interfused within the porous cross-linked polyimide network. Polyim ide-urea-network battery-separator compositions also are disclosed. Voltaic cells comprising a cathode, an anode, and the polyimide-network battery separator composition or the polyimide-urea-network battery separator composition are also disclosed.

The present invention relates to a composition for a gel polymer electrolyte, in which liquid injection characteristics at room temperature and in an oxygen atmosphere are improved by including a non-fluoride oxygen scavenger as well as a polymerizable oligomer having a polymerizable substituent, and a lithium secondary battery in which capacity retention with cycles is excellent by including a gel polymer electrolyte which is formed by using the composition.