Disclosed are stable zero-valent metal and oxidized black carbon admixtures and their use, to catalyze rapid reductive degradation reactions in aqueous solutions. The compositions and remediation methods are used in the non-explosive neutralization and decomposition of ammonium nitrate.

Metal ion-directed carboxylic acid functionalized polyoxometalate hybrid compounds, and their preparation method and applications in catalyzing the degradation of chemical warfare agent simulants. In the synthesis, Na.sub.2MoO.sub.4, p-hydroxybenzonic acid (PHBA), alanine (Ala), KCl, transition metal cations and As.sub.2O.sub.3 as raw materials and water are used as solvent. At room temperature, 2-chloroethyl ethyl sulfide (CEES) and the prepared polyoxometalate hybrid compounds were mixed together in anhydrous ethanol and stirred, and H.sub.2O.sub.2 was subsequently added into the reaction system. The catalytic reaction for the degradation of CEES was finished within 5 min under stirring. In the catalytic hydrolysis of diethyl cyanophosphonate (DECP), the catalyst, DECP, DMF and H.sub.2O were put together and mixed fully. The prepared polyoxometalate hybrid compounds have the advantages of high conversion, high selectivity and easy recyclability in catalyzing the degradation of two types of chemical warfare agent simulant.

Metal ion-directed carboxylic acid functionalized polyoxometalate hybrid compounds, and their preparation method and applications in catalyzing the degradation of chemical warfare agent simulants. In the synthesis, Na.sub.2MoO.sub.4, p-hydroxybenzonic acid (PHBA), alanine (Ala), KCl, transition metal cations and As.sub.2O.sub.3 as raw materials and water are used as solvent. At room temperature, 2-chloroethyl ethyl sulfide (CEES) and the prepared polyoxometalate hybrid compounds were mixed together in anhydrous ethanol and stirred, and H.sub.2O.sub.2 was subsequently added into the reaction system. The catalytic reaction for the degradation of CEES was finished within 5 min under stirring. In the catalytic hydrolysis of diethyl cyanophosphonate (DECP), the catalyst, DECP, DMF and H.sub.2O were put together and mixed fully. The prepared polyoxometalate hybrid compounds have the advantages of high conversion, high selectivity and easy recyclability in catalyzing the degradation of two types of chemical warfare agent simulant.

Compositions and methods for oxidizing organic contaminants while sequestering inhibitory forms of carbon. An oxidant capable of producing free radicals oxidizes organic contaminants. A metal oxide, metal hydroxide, or metal peroxide generates a soluble hydroxide concentration of about 1×10.sup.−4 M or greater to convert carbonic acid, bicarbonate ion, methane, elemental carbon, and other organic forms of carbon to carbonate ion. A metal having a carbonate with a lower solubility product constant than its hydroxide precipitates the carbonate ion as a metal carbonate, thereby eliminating soluble carbonate as a radical scavenger. Compositions and methods that additionally minimize metal solubilization and sequester solubilized metals are also disclosed.

Compositions and methods for oxidizing organic contaminants while sequestering inhibitory forms of carbon. An oxidant capable of producing free radicals oxidizes organic contaminants. A metal oxide, metal hydroxide, or metal peroxide generates a soluble hydroxide concentration of about 1×10.sup.−4 M or greater to convert carbonic acid, bicarbonate ion, methane, elemental carbon, and other organic forms of carbon to carbonate ion. A metal having a carbonate with a lower solubility product constant than its hydroxide precipitates the carbonate ion as a metal carbonate, thereby eliminating soluble carbonate as a radical scavenger. Compositions and methods that additionally minimize metal solubilization and sequester solubilized metals are also disclosed.

There are disclosed processes for destructing a toxic chemical including the steps of mixing the toxic chemical with a liquid phase formed by an aqueous mixture of water and an ionic liquid or molten salt which is miscible with water, the ionic liquid or molten salt comprising a tertiary amine group or quaternary ammonium group; and contacting the toxic chemical in the liquid phase with the ionic liquid or molten salt so as to decompose the toxic chemical.

There are disclosed processes for destructing a toxic chemical including the steps of mixing the toxic chemical with a liquid phase formed by an aqueous mixture of water and an ionic liquid or molten salt which is miscible with water, the ionic liquid or molten salt comprising a tertiary amine group or quaternary ammonium group; and contacting the toxic chemical in the liquid phase with the ionic liquid or molten salt so as to decompose the toxic chemical.

A secured “smart” container is disclosed for collecting green waste products including operational functions for collection, video surveillance and monitoring capacity. The secured “smart” container may include one or more programmable logic controllers. Operational functions are performed by electrical components including sensors to determine green waste deposits characteristics and contents. Operational functions are further adapted to send and receive data, operationally wirelessly, and configured and adapted to utilize solar derived electric power and, optionally, electric power from other sources. Embodiments provide constant 24 hour/7 days a week video surveillance and alert monitoring capabilities. Disclosed systems and methods also include collection and transportation of waste contents from the container to a processing subsystem. Additionally, disclosed systems may also include a monitoring system for monitoring the collection of green waste product, delivery of the same to the processing subsystem and tracking to and throughout final processing of the green waste product and handling personnel.

A composition having a gadolinium-, samarium-, or lanthanum-substituted porous cerium oxide and copper or gold nanoparticles. The composition can be exposed to electromagnetic radiation to form reactive oxygen species in the composition to decompose organophosphonate compounds. The composition may be made by forming a mixture of a cerium salt; a gadolinium, samarium, or lanthanum salt; and an epoxide; forming gel from the mixture; and drying the gel to form an aerogel, a xerogel, or an ambigel. Copper or gold nanoparticles are added or formed at any point in the method.

A composition having a gadolinium-, samarium-, or lanthanum-substituted porous cerium oxide and copper or gold nanoparticles. The composition can be exposed to electromagnetic radiation to form reactive oxygen species in the composition to decompose organophosphonate compounds. The composition may be made by forming a mixture of a cerium salt; a gadolinium, samarium, or lanthanum salt; and an epoxide; forming gel from the mixture; and drying the gel to form an aerogel, a xerogel, or an ambigel. Copper or gold nanoparticles are added or formed at any point in the method.