An energy storage device includes an anode, a cathode, and a separator disposed between the anode and the cathode. At least one of the anode, cathode and separator includes a copolymer functioning as a non-aqueous adhesive and/or solid-state electrolyte for the energy storage device. The copolymer is a copolymer or a derivative thereof, which is produced by polymerization of monomers containing conductive ion group and/or olefinic monomers in the presence of 2-propenenitrile. Therefore, the energy storage device which the copolymer is used therein has excellent charging and discharging performance to therefore effectively enhance the efficiency and extend the service life of the energy storage device.

An energy storage device comprises two electrodes; and a separator disposed between the electrodes; wherein at least one of the electrodes and the separator comprises a copolymer, which serves as a non-aqueous binder and/or solid electrolyte for the electrodes and the separator of the energy storage device, and the copolymer is a copolymerized product or its derivative formed by the polymerization reaction of acrylonitrile and vinyl acetate. Therefore, the charge and discharge properties of the energy storage device using the copolymer can be improved, thereby effectively extending the efficiency and lifetime of the energy storage device.

An energy storage device includes an anode, a cathode, and a separator disposed between the anode and the cathode. At least one of the anode, cathode and separator includes a copolymer functioning as a non-aqueous adhesive and/or solid-state electrolyte for the energy storage device. The copolymer is a copolymer or a derivative thereof, which is produced by polymerization of monomers containing conductive ion group and/or olefinic monomers in the presence of 2-propenenitrile. Therefore, the energy storage device which the copolymer is used therein has excellent charging and discharging performance to therefore effectively enhance the efficiency and extend the service life of the energy storage device.

A method for the production of paper or cardboard is provide comprising the following steps: (A) Adding a water soluble polymer P to a first aqueous pulp suspension, wherein polymer P is obtainable by Polymerizing to a polymer V of (i) 33 to 83 mol % of a monomer of formula I

##STR00001## in which R.sup.1H or C.sub.1-C.sub.6 alkyl, (ii) 6 to 56 mol % of diallyl dimethyl ammonium chloride, diallyl diethyl ammonium chloride or a salt form of a monoethylenically unsaturated monomer, (iii) 11 to 61 mol % of a monoethylenically unsaturated carboxylic acid, sulfonic acid or phosphonic acid, or salt forms thereof, (iv) 0 to 50 mol % of one or more ethylenically unsaturated monomers, and hydrolyzing the NC(O)R.sup.1 groups to form primary amino or amidine groups, (B) dehydrating the second aqueous pulp suspension to a wet paper structure, (C) dehydrating the wet paper structure.

Hydrogel materials used in the manufacture of biocompatible medical devices, for example, hydrogel materials having desirable physical properties for use as a contact lens. A composition contains at least one vinyl containing monomer, a methacrylate(acrylate) monomer, methacrylate (acrylate) prepolymers, crosslinking agents and monomers having the structure as shown in Formula 1:

##STR00001##

where R.sup.1 is a vinyl functionality capable of radical polymerization with specific preference for N-vinyl lactam derivatives and R.sup.2 is a zwitterionic functionality. The materials utilize a two-phase polymerization strategy.

In an embodiment, the present disclosure pertains to a method of changing the glass transition temperature of a polymer. In some embodiments, the polymer includes at least one hydrazone-containing compound. In general, the methods of the present disclosure include one or more of the following steps of: (1) applying light to the polymer; and (2) thereby changing the glass transition temperature of the polymer. In another embodiment, the present disclosure pertains to a polymer having a light-adjustable glass transition temperature. In some embodiments, the polymer includes at least one hydrazone-containing compound.

In an embodiment, the present disclosure pertains to a method of changing the glass transition temperature of a polymer. In some embodiments, the polymer includes at least one hydrazone-containing compound. In general, the methods of the present disclosure include one or more of the following steps of: (1) applying light to the polymer; and (2) thereby changing the glass transition temperature of the polymer. In another embodiment, the present disclosure pertains to a polymer having a light-adjustable glass transition temperature. In some embodiments, the polymer includes at least one hydrazone-containing compound.

A personal care conditioning and/or styling composition for a keratin substrate comprising: (A) at least one conditioning and/or styling ter/tetra polymer obtained by polymerizing: (i) about 50 wt. % to 97 wt. % of at least one cationic or pseudo-cationic monomer selected from the group consisting of diallyl dimethyl ammonium chloride (DADMAC), Hydroxyethyl-pyrrolidone-methacrylate (MO6), and/or Vinylpyrrolidone (VP); (ii) about 1 wt. % to 30 wt. % of at least one anionic monomer selected from the group consisting of (a) acrylic acid (AA), (b) acrylamido methylpropyl sulfonate (AMPS), and/or (c) sodium methyl allyl sulfonate (SMAS); and (iii) about 0.1 wt. % to 20 wt. % of at least one hydrophobic monomer selected from the group consisting of (a) polyoxyethylene (PEG)-18-behenylether-methacrylate (BEM) (b) Lauryl-ethoxylated-methacrylate (LEM), (c) stearyl acrylate (SA), (d) Streath-10-allyl-ether, and/or (e) Vinylcaprolactam (V-cap); and wherein said ter/tetra polymer has a cationic degree of substitution (Cat-DS) of greater than about 0.001 units, and wherein the cationic charge density is in the range of about 1 meq/g to about 6.5 meq/g; (B) at least one cosmetically acceptable excipient; and (C) optionally, at least one effective amount of personal care active ingredient. Also, disclosed is a process of preparing said ter/tetra polymer, and its method of use.

A personal care conditioning and/or styling composition for a keratin substrate comprising: (A) at least one conditioning and/or styling ter/tetra polymer obtained by polymerizing: (i) about 50 wt. % to 97 wt. % of at least one cationic or pseudo-cationic monomer selected from the group consisting of diallyl dimethyl ammonium chloride (DADMAC), Hydroxyethyl-pyrrolidone-methacrylate (MO6), and/or Vinylpyrrolidone (VP); (ii) about 1 wt. % to 30 wt. % of at least one anionic monomer selected from the group consisting of (a) acrylic acid (AA), (b) acrylamido methylpropyl sulfonate (AMPS), and/or (c) sodium methyl allyl sulfonate (SMAS); and (iii) about 0.1 wt. % to 20 wt. % of at least one hydrophobic monomer selected from the group consisting of (a) polyoxyethylene (PEG)-18-behenylether-methacrylate (BEM) (b) Lauryl-ethoxylated-methacrylate (LEM), (c) stearyl acrylate (SA), (d) Streath-10-allyl-ether, and/or (e) Vinylcaprolactam (V-cap); and wherein said ter/tetra polymer has a cationic degree of substitution (Cat-DS) of greater than about 0.001 units, and wherein the cationic charge density is in the range of about 1 meq/g to about 6.5 meq/g; (B) at least one cosmetically acceptable excipient; and (C) optionally, at least one effective amount of personal care active ingredient. Also, disclosed is a process of preparing said ter/tetra polymer, and its method of use.

Hydrogel materials used in the manufacture of biocompatible medical devices, for example, hydrogel materials having desirable physical properties for use as a contact lens. A composition contains at least one vinyl containing monomer, a methacrylate(acrylate) monomer, methacrylate (acrylate) prepolymers, crosslinking agents and monomers having the structure as shown in Formula 1:

##STR00001##

where R.sup.1 is a vinyl functionality capable of radical polymerization with specific preference for N-vinyl lactam derivatives and R.sup.2 is a zwitterionic functionality. The materials utilize a two-phase polymerization strategy.