The present invention concerns a process for manufacturing a porous carbonaceous monolith structure comprising the steps of (i) introducing a precursor material comprising particles comprising a halogenated polymer having a melting point in a mold; (ii) forming a shaped body comprising aggregates of the particles of the precursor material, by concurrently applying to the precursor material a pressure P ranging from 10 to 300 bars when the halogenated polymer is a vinylidene chloride homopolymer and from 10 to 150 bars when the halogenated polymer differs from a vinylidene chloride homopolymer, and maintaining the precursor material at a temperature T.sub.1 ranging from T.sub.1,min=20° C. to T.sub.1,max=T.sub.m−50° C. wherein T.sub.m is the melting point of the halogenated polymer, and; (iii) optionally cooling then demolding the shaped body; (iv) introducing the shaped body in a furnace; (v) causing the pyrolysis of the halogenated polymer in the furnace until the porous carbonaceous monolith structure is obtained.

[SUMMARY]

[OBJECT] To provide a per- and polyfluoroalkyl compound-adsorbing activated carbon having a high collection rate of per- and polyfluoroalkyl compounds in an atmospheric sample, and a filter body using the same.

[ACHIEVING MEANS] A per- and polyfluoroalkyl compound-adsorbing activated carbon for desorbably adsorbing per- and polyfluoroalkyl compounds in an atmospheric sample, the activated carbon including an activated carbon adsorbent having a BET specific surface area of 900 m.sup.2/g or more, a sum (V.sub.mic) of a volume of micropores of 1 nm or less of 0.35 cm.sup.3/g or more, a sum (V.sub.met) of a volume of mesopores of 2 to 60 nm of 0.02 cm.sup.3/g or more, a volume difference (V.sub.s) between the micropore volume (V.sub.mic) and the mesopore volume (V.sub.met) of 0.45 or more, and a surface oxide amount of 0.10 meq/g or more.

Embodiments of the present disclosure provide for metal-organic materials (MOMs), systems that exhibit permanent porosity and using hydrophobic MOMs to separate components in a gas, methods of separating CO.sub.2 from a gas, and the like.

Provided herein are electret-MOF filter embedded with particles derived from metal-organic frameworks (MOF) and their methods of manufacturing. The methods of manufacturing the electret-MOF filter can include suspending MOF particles in a solvent to form a MOF particle mixture, contacting a charged polymeric fibrous web with the MOF particle mixture, and coating the charged polymeric fibrous web with the MOF particles by flowing the MOF particle mixture through an inverse side of the polymeric fibrous web. The disclosed coating method can deposit MOF particles uniformly, without formation of films at interstitial spaces between fibers. The electret-MOF filter can simultaneously remove fine particulate matters (PMs) and hazardous gaseous pollutants (including volatile organic compounds (VOCs)) with high particle holding and gas adsorption capacities, and with very low air resistance.

A multi-functional composition of matter that is useful for injection into a flue gas stream to rapidly and efficiently remove mercury from the flue gas streams, particularly at above average flue stream temperatures of about 340° F. or higher. The multi-functional composition of matter may include a fixed carbon content of at least about 20 wt. %, a mineral content of from about 20 wt. % to about 50 wt. %, a sum of micropore plus mesopore volume of at least about 0.20 cc/g, a micropore volume to mesopore volume ratio of at least about 0.7, and a tapped density of not greater than about 0.575 g/ml. These compositions may be further characterized by number of particles per gram of the composition of matter such that the composition may have at least about 0.8 billion particles per gram, or even as many as 1.5 billion particles per gram. These physical and chemical properties may enhance (1) the oxidation reaction kinetics for the oxidation of mercury species, (2) frequency of contact events, and (3) capture and sequestration of mercury, to achieve efficient mercury capture by the composition even in high temperature flue gas streams.

This disclosure provides a halogenated activated carbon composition comprising carbon, a halogenated compound and a salt. In some embodiments, the halogenated compound and the salt comprise a naturally occurring salt mixture, as may be obtained from ocean water, salt lake water, rock salt, salt brine wells, for example. In some embodiments, the naturally occurring salt mixture comprises Dead Sea salt.

A device that retains high moisture capacity in the presence of certain contaminants. The device can include a substrate and a desiccant. The device can be configured in relation to an enclosure such that the device absorbs and desorbs moisture from the enclosure.

Novel radioactive iodide molecular traps, in which one or more metal atoms are functionalized by coordinating to an amine containing two or more nitrogens, and methods of using the molecular traps to capture radioactive iodide.

A method for producing a carbon fiber material is disclosed, the method comprising the steps of a) Preparation of a solution of polyacrylonitrile in a suitable organic solvent b) Electrospinning of the solution obtained in a) and drying of the obtained fiber material c) Crosslinking of the obtained fiber material by heating to 150 to 350° C. in an air or oxygen atmosphere for 1 to 30 h d) Carbonization of the obtained fiber material in an inert gas atmosphere at a temperature in the range of 500 to 2,500° C., characterized in that no silicon, sulfur, metal compounds, intermetallic compounds, silicon compounds and/or sulfur compounds are added to the polyacrylonitrile solution in step a) and that neither stabilization nor surface modification steps are carried out with the fiber material by treatment with chemical reagents and/or exposure to tensile stress.

Also disclosed is a carbon fiber material obtainable by the above process, as well as a carbon fiber material, characterized in that it has a proportion of ultramicropores V.sub.<0.4 nm of 0.01 to 10, more preferably 0.02 to 5, even more preferably 0.025 to 0.1, most preferably 0.03 to 0.06 cm.sup.3/g, determined by CO.sub.2 adsorption tests and evaluation with DFT and GC-MC simulation.

The present disclosure relates to a chabazite-type zeolite, comprising at least two cages composed of 4- and 8-membered rings connected by one 6-membered double ring, remarkable in that it has a Si/Al molar ratio comprised between 1 and 15, in that it comprises caesium and potassium with a Cs/K molar ratio of at most 5.0 and in that it forms nanoparticles with an average crystal size comprised between 5 nm and 250 nm and with a specific surface area comprised between 50 m.sup.2g.sup.−1 and 200 m.sup.2g.sup.−1. Amorphous precursors, devoid of an organic structure-directing agent, as well as a method for preparation of these amorphous precursors in the absence of such organic structure-directing agent and method for preparation of the chabazite-type zeolite, are also described. Finally, the use of the chabazite-type zeolite as a sorbent for carbon dioxide is also demonstrated.