A method comprising a) mixing and dissolving the solid hazardous heavy metal-containing composition with an acid solution; b) precipitating the heavy metal from the hazardous heavy metal acid composition; c) precipitating the heavy metal from the hazardous heavy metal acid composition with a heavy metal-precipitation agent; and d) separating out the heavy metal precipitate from the aqueous supernatant, whereby the heavy metal-precipitation agent comprises a diorgano-dithiophosphinic acid or the alkali metal or ammonia salts thereof.

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A method comprising a) mixing and dissolving the solid hazardous heavy metal-containing composition with an acid solution; b) precipitating the heavy metal from the hazardous heavy metal acid composition; c) precipitating the heavy metal from the hazardous heavy metal acid composition with a heavy metal-precipitation agent; and d) separating out the heavy metal precipitate from the aqueous supernatant, whereby the heavy metal-precipitation agent comprises a diorgano-dithiophosphinic acid or the alkali metal or ammonia salts thereof.

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A contaminant-sequestering coating includes a network of hydrolyzed silane compounds. The hydrolyzed silane compounds include a hydrophilic polar head region, a hydrophobic linker, and an anchor region including a silicon atom. The network of hydrolyzed silane compounds is devoid or substantially devoid of fluorine atoms. Methods of destroying one or more perfluoroalkyl and/or polyfluoroalkyl (PFAS) compounds present in a contaminant-containing liquid are also provided.

A contaminant-sequestering coating includes a network of hydrolyzed silane compounds. The hydrolyzed silane compounds include a hydrophilic polar head region, a hydrophobic linker, and an anchor region including a silicon atom. The network of hydrolyzed silane compounds is devoid or substantially devoid of fluorine atoms. Methods of destroying one or more perfluoroalkyl and/or polyfluoroalkyl (PFAS) compounds present in a contaminant-containing liquid are also provided.

Materials for decontamination of compounds having a phosphorous-sulfur bond or a phosphorous-oxygen bond. A porous polymer, such as poly(dicyclopentadiene), contains particles of zirconium hydroxide. The polymer optionally has hydroperoxide groups.

A composite material is provided comprising a porous polymeric matrix having metal-organic framework (MOF) domains dispersed within the porous polymeric matrix, each of said MOF domains in fluid communication with the external environment through the pores in the porous polymeric matrix. A process of using the composite material to chemically modify or detoxify a chemical warfare agent or a toxic industrial chemical is also provided. The chemical warfare agent or the toxic industrial chemical is brought into contact with a MOF domain within the porous polymeric matrix so that the MOFs adsorb and chemically modify the chemical warfare agent or the toxic industrial chemical. A process for producing such a composite material is also disclosed.

A composite material is provided comprising a porous polymeric matrix having metal-organic framework (MOF) domains dispersed within the porous polymeric matrix, each of said MOF domains in fluid communication with the external environment through the pores in the porous polymeric matrix. A process of using the composite material to chemically modify or detoxify a chemical warfare agent or a toxic industrial chemical is also provided. The chemical warfare agent or the toxic industrial chemical is brought into contact with a MOF domain within the porous polymeric matrix so that the MOFs adsorb and chemically modify the chemical warfare agent or the toxic industrial chemical. A process for producing such a composite material is also disclosed.

An adsorbent and photocatalytic decontamination gel consisting of a colloidal solution comprising, preferably consisting of: 8% to 30% by weight, preferably 10% to 30% by weight, more preferably 15% to 20% by weight, better still 15% to 20% by weight, the value 15% being excluded, even better still 16% to 20% by weight, for example 20% by weight of TiO.sub.2, optionally doped, relative to the weight of the gel; optionally 0.01% to 10% by weight, preferably 0.1% to 5% by weight, relative to the weight of the gel, of at least one dye and/or of at least one pigment; optionally 0.1% to 2% by weight, relative to the weight of the gel, of at least one surfactant; optionally 0.05% to 5% by weight, preferably 0.05% to 2% by weight, relative to the weight of the gel, of at least one superabsorbent polymer; and the balance of solvent.

Disclosed is a method of decontamination by exposing a zirconium oxy(hydroxide) aerogel to a liquid, vapor, or gaseous sample suspected of containing a phosphonate compound. The aerogel may be doped with Fe.sup.3+ ions, Ce.sup.3+ ions, or SO.sub.4.sup.2− ions. The aerogel may be made by: providing a solution of ZrCl.sub.4; FeCl.sub.3, CeCl.sub.3, or Zr(SO.sub.4).sub.2; and a solvent; adding a cyclic ether to the solution to form a gel; infiltrating the gel with liquid carbon dioxide; applying a temperature and pressure to form supercritical fluid carbon dioxide; and removing the carbon dioxide for form an aerogel.

The present invention relates to a method for modifying a textile yarn or fabric by immobilising a cyclodextrin derivative on said yarn or fabric, said process comprising a step (a) of contacting said textile yarn or fabric with said cyclodextrin derivative and with a bridging agent such as 1,2,3,4-butanetetracarboxylic acid, optionally in the presence of a catalyst such as cyanamide,

to obtain a textile yarn or fabric on which the cyclodextrin derivative of formula (I) is immobilised.