A fluorescent water treatment polymer comprises at least one water soluble carboxylic acid monomer other than maleic acid, at least one sulfonated pyrene-containing fluorescent monomer, and at least one phosphino group wherein the phosphorous atom of the phosphino group is in the polymer backbone. Additional monomers can be present, with the proviso that if maleic acid is present it comprises no greater than 75 mol % of the polymer. Surprisingly, it has been found that when the phosphino group is present the polymers exhibit an unexpectedly strong fluorescent signal strength. The signal strength of the fluorescent monomer in the polymer is further enhanced when the polymer comprises no greater than 75 mol % maleic acid.

A composition of matter including a mother solution; an organic ester; an additive agent and deionized water. The mother solution includes a rare earth compound or a metal compound, an organic acid, an organic amine, and deionized water. Also provided is a method of preparing the composition of matter. The method includes: 1) heating deionized water to a temperature of 50-60 C.; adding an organic acid to the deionized water, allowing to dissolve, followed by addition of a rare earth compound or a metal compound, 2-4 hours later, adding an organic amine, heating to a temperature of 70-80 C. and holding; cooling and filtering to yield a mother solution; 2) mixing the mother solution, deionized water, and a catalyst; vacuumizing a resulting mixture, heating the mixture to a temperature of 95-125 C. and holding, following by addition of a polymerization inhibitor and an organic ester; 2-4 hours later, cooling, standing, separating.

A composition of matter including a mother solution; an organic ester; an additive agent and deionized water. The mother solution includes a rare earth compound or a metal compound, an organic acid, an organic amine, and deionized water. Also provided is a method of preparing the composition of matter. The method includes: 1) heating deionized water to a temperature of 50-60 C.; adding an organic acid to the deionized water, allowing to dissolve, followed by addition of a rare earth compound or a metal compound, 2-4 hours later, adding an organic amine, heating to a temperature of 70-80 C. and holding; cooling and filtering to yield a mother solution; 2) mixing the mother solution, deionized water, and a catalyst; vacuumizing a resulting mixture, heating the mixture to a temperature of 95-125 C. and holding, following by addition of a polymerization inhibitor and an organic ester; 2-4 hours later, cooling, standing, separating.

Cross-linked polyvinyl polymers comprising charged groups and methods of making are disclosed. The polymers are effective and durable adsorbent of dyes from aqueous solutions. Also, a method of removal of dyes from contaminated water is disclosed.

A poly(vinylphosphonic acid) (PVPA)-(NH.sub.4).sub.2MoO.sub.4), gel polymer electrolyte can be prepared by incorporating redox-mediated Mo, or similar metal, into a PVPA, or similar polymer, matrix. Gel polymer electrolytes including PVPA/MoX, x representing the percent fraction Mo in PVPA, can be used to make supercapacitors including active carbon electrodes. The electrolytes can be in gel form, bendable and stretchable in a device. Devices including this gel electrolyte can have a specific capacitance (Cs) of 1276 F/g, i.e., a more than 50-fold increase relative to a PVPA system without Mo. A PVPA/Mo10 supercapacitor can have an energy density of 180.2 Wh/kg at power density of 500 W/kg, and devices with this hydrogel structure may maintain 85+% of their initial capacitance performance after 2300 charge-discharge cycles.

A poly(vinylphosphonic acid) (PVPA)-(NH.sub.4).sub.2MoO.sub.4), gel polymer electrolyte can be prepared by incorporating redox-mediated Mo, or similar metal, into a PVPA, or similar polymer, matrix. Gel polymer electrolytes including PVPA/MoX, x representing the percent fraction Mo in PVPA, can be used to make supercapacitors including active carbon electrodes. The electrolytes can be in gel form, bendable and stretchable in a device. Devices including this gel electrolyte can have a specific capacitance (Cs) of 1276 F/g, i.e., a more than 50-fold increase relative to a PVPA system without Mo. A PVPA/Mo10 supercapacitor can have an energy density of 180.2 Wh/kg at power density of 500 W/kg, and devices with this hydrogel structure may maintain 85+% of their initial capacitance performance after 2300 charge-discharge cycles.

Cross-linked polyvinyl polymers comprising charged groups and methods of making are disclosed. The polymers are effective and durable adsorbent of dyes from aqueous solutions. Also, a method of removal of dyes from contaminated water is disclosed.

Cross-linked polyvinyl polymers comprising charged groups and methods of making are disclosed. The polymers are effective and durable adsorbent of dyes from aqueous solutions. Also, a method of removal of dyes from contaminated water is disclosed.

The invention provides a radically polymerizable compound wherein an acid group is joined via a spacer group to a polyethyleneimine group. The polyethyleneimine group has at least one radically polymerizable group in the side chain and/or terminally. The invention relates further to a process for preparing such compounds by cationic polymerization of oxazolines, to the use of such compounds as constituents of a dental material, and to a dental material comprising the compounds of the invention.

The invention provides a radically polymerizable compound wherein an acid group is joined via a spacer group to a polyethyleneimine group. The polyethyleneimine group has at least one radically polymerizable group in the side chain and/or terminally. The invention relates further to a process for preparing such compounds by cationic polymerization of oxazolines, to the use of such compounds as constituents of a dental material, and to a dental material comprising the compounds of the invention.