A process for forming a pure carbon product has the steps of soaking charcoal with hydrochloric acid to remove solids from the charcoal, removing the hydrochloric acid from the soaked charcoal, drying the charcoal, grinding the dried charcoal into a fine powder, mixing water with the fine powder, washing the fine powder, removing the water so as to from a charcoal slurry, and drying the charcoal slurry so as to form the pure carbon powder. The charcoal slurry has a skim on the surface thereof. The skim is removed.

A method for creating a metal-carbon composite. In one embodiment, the method includes the steps of providing a polymer Schiff base transition metal .[.film.]. .Iadd.complex .Iaddend.precursor .Iadd.film .Iaddend.having a chemical structure of the formula [M(Schiff)].sub.n and a recurring unit and a transition metal selected from the group consisting of nickel, palladium, platinum, cobalt, copper, iron; Schiff is a tetradentate Schiff base ligand selected from the group consisting of Salen (residue of bis(salicylaldehyde)-ethylenediamine), Saltmen (residue of bis(salicylaldehyde)-tetramethylethylenediamine, Salphen (residue of bis-(salicylaldehyde)-o-phenylenediamine), a substituent in a Schiff base is selected from the group consisting of H—, and carbon-containing substituents, preferably CH.sub.3—, C.sub.2H.sub.5—, CH.sub.3O—, C.sub.2H.sub.5O—, and Y is a bridge in a Schiff base depositing the polymer Schiff base transition metal precursor film onto a support substrate; and heating the polymer Schiff base transition metal .Iadd.complex .Iaddend.precursor film and support substrate in a furnace in an inert atmosphere.

A method for creating a metal-carbon composite. In one embodiment, the method includes the steps of providing a polymer Schiff base transition metal .[.film.]. .Iadd.complex .Iaddend.precursor .Iadd.film .Iaddend.having a chemical structure of the formula [M(Schiff)].sub.n and a recurring unit and a transition metal selected from the group consisting of nickel, palladium, platinum, cobalt, copper, iron; Schiff is a tetradentate Schiff base ligand selected from the group consisting of Salen (residue of bis(salicylaldehyde)-ethylenediamine), Saltmen (residue of bis(salicylaldehyde)-tetramethylethylenediamine, Salphen (residue of bis-(salicylaldehyde)-o-phenylenediamine), a substituent in a Schiff base is selected from the group consisting of H—, and carbon-containing substituents, preferably CH.sub.3—, C.sub.2H.sub.5—, CH.sub.3O—, C.sub.2H.sub.5O—, and Y is a bridge in a Schiff base depositing the polymer Schiff base transition metal precursor film onto a support substrate; and heating the polymer Schiff base transition metal .Iadd.complex .Iaddend.precursor film and support substrate in a furnace in an inert atmosphere.

Provided is a preparation method and use method of a material for deep purification of HF electronic gas. A metal fluoride-loaded activated carbon material AC/MFx.nH20 is prepared, and a mixed gas flow of carbonyl fluoride and high-purity nitrogen is used to deeply dehydrate the material to obtain the material for deep purification of HF electronic gas AC/MFx. This kind of material has fluoride that can form crystal water to form hydrated metal fluoride, and has strong water absorption properties. Moreover, the anhydrous fluoride and activated carbon do not have to face the problem of being corroded by HF, and the collapse of framework structure and the secondary pollution to HF from reaction products would not be caused. The material has the advantages of high purity and extremely low moisture content when being used for efficiently removing moisture in HF.

Provided is a preparation method and use method of a material for deep purification of HF electronic gas. A metal fluoride-loaded activated carbon material AC/MFx.nH20 is prepared, and a mixed gas flow of carbonyl fluoride and high-purity nitrogen is used to deeply dehydrate the material to obtain the material for deep purification of HF electronic gas AC/MFx. This kind of material has fluoride that can form crystal water to form hydrated metal fluoride, and has strong water absorption properties. Moreover, the anhydrous fluoride and activated carbon do not have to face the problem of being corroded by HF, and the collapse of framework structure and the secondary pollution to HF from reaction products would not be caused. The material has the advantages of high purity and extremely low moisture content when being used for efficiently removing moisture in HF.

Provided is a purification material capable of highly efficiently removing contaminant components from water. A water purification material has a composition represented by a mixing ratio of zeolite, ferric hydroxide, activated carbon, titanium oxide, and magnesium hydroxide of 6 to 7:1 to 2:0.5 to 1:0.01 to 0.05:0.01 to 0.10 in terms of weight ratio.

Provided is a purification material capable of highly efficiently removing contaminant components from water. A water purification material has a composition represented by a mixing ratio of zeolite, ferric hydroxide, activated carbon, titanium oxide, and magnesium hydroxide of 6 to 7:1 to 2:0.5 to 1:0.01 to 0.05:0.01 to 0.10 in terms of weight ratio.

A sorbent composition for the sequestration of mercury from a gas stream, a method for sequestering mercury from a gas stream and a method for the manufacture of a sorbent composition. The sorbent composition includes a highly porous particulate sorbent and at least two additive components, namely a non-halogen metal compound comprising a metal cation and an inorganic sulfur-containing compound, where at least a portion of the sulfur in the sulfur-containing compound has an oxidation state of equal to or less than +4. The method includes injecting the highly porous particulate sorbent and the two additive components into a gas stream, either discretely or as a single sorbent composition, to sequester mercury in the particulate sorbent. The method has a high degree of efficacy for mercury removal without requiring the addition of halogens to the gas stream.

The present description provides low DBL bleed emission performance properties that allows the design of evaporative fuel emission control systems that are simpler and more compact than those possible by prior art by inclusion of a vent-side volume comprising a parallel passage adsorbent such as a carbon honeycomb with narrow channel width and low cell pitch.

The present description provides low DBL bleed emission performance properties that allows the design of evaporative fuel emission control systems that are simpler and more compact than those possible by prior art by inclusion of a vent-side volume comprising a parallel passage adsorbent such as a carbon honeycomb with narrow channel width and low cell pitch.