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.

Porous cellulose microparticles and their use in, inter alias, cosmetic and pharmaceutic preparations are provided. These microparticles comprise cellulose I nanocrystals aggregated together, thus forming the microparticles, and arranged around cavities in the microparticles, thus defining pores in the microparticles. A method of for producing these microparticles is also provided. It involves mixing a suspension of cellulose I nanocrystals with an emulsion of a porogen to produce a mixture comprising a continuous liquid phase in which droplets of the porogen are dispersed and in which the nanocrystals of cellulose I are suspended; spray-drying the mixture to produce microparticles; and if the porogen has not sufficiently evaporated during spray-drying to form pores in the microparticles, evaporating the porogen or leaching the porogen out of the microparticles to form pores in the microparticles.

A reversible enrichment material, its preparation and application thereof are provided. The reversible enrichment material includes an inorganic carrier; and an active metal salt, a first metal salt promoter and a second metal salt promoter supported on the inorganic carrier. The active metal salt is a soluble silver salt, a soluble copper salt, or a combination thereof. The first metal salt promoter is one or more selected from the group consisting of soluble salts of Group IA, Group IIA and Group IIIA metals, and the second metal salt promoter is one or more selected from the group consisting of soluble salts of transition metals other than Group IB metals. The reversible enrichment material can realize effective separation of saturated hydrocarbon from unsaturated hydrocarbon and has good reversibility.

A biochar-derived adsorbent preferably from Sargassum boveanum, macroalgae can be used for removing phenolic compounds, such as 2,4,6-trichlorophenol and 2,4-dimethylphenol, from aqueous solutions. The carbonization can improve the removal capability of the macroalgae adsorbent for such phenolic compounds with removal efficiencies of 60% or more from high salinity seawater and 100% from distilled water. The adsorption may occur through a mixed mechanism dominated by physisorption following pseudo second-order kinetics. The adsorption of the phenolic molecules may be spontaneous, endothermic and thermodynamically favorable.

Disclosed herein are composite materials and methods of making and use thereof. The composite materials comprise: a carbon nanotube and a plurality of ferrihydrite particles disposed on the carbon nanotube, the composite material comprising the plurality of ferrihydrite particles and the carbon nanotube in a weight ratio of from 5:95 to 95:5. The weight ratio can be selected such that the composite material has a desired balance between specific surface area and specific capacitance. Also disclosed herein are methods comprising: making a plurality of the composite materials, the weight ratio of the plurality of ferrihydrite particles and the carbon nanotube being different for each composite material; and determining and comparing the specific surface area and specific surface capacitance for the plurality of composite materials to determine the weight ratio at which the composite material has a desired balance between the specific surface area and the specific capacitance.

A composite material for floating on a contaminated water source, including: A) a polymeric structure having a network of interconnected porous channels; and B) a carbonous material dispersed within the polymeric structure, the carbonous material has a functionalized surface. The composite material has a density of less than 1 g/cm.sup.3, and the contaminated water source contains a low-boiling-point contaminant. The polymeric structure draws contaminated water from the contaminated water source into the polymeric structure via capillary action, and the functionalized surface removes the low-boiling point contaminant from the contaminated water. A method of purifying water using the composite material as mentioned herein and a kit for harvesting purified water including the composite material as mentioned herein.

Systems and Methods to produce a lime hydrate sorbent composition formed of highly reactive lime hydrate (HRH) by adding compounds to the slaking water in a method that would produce a non-HRH, which will typically be a lime hydrate having citric acid reactivity as discussed above of more than ten seconds, to make the non-HRH an HRH, which is having a citric acid reactivity of less than or equal to ten seconds.

The present invention provides that powder is mainly constituted from secondary particles of hydroxyapatite. The secondary particles are obtained by drying a slurry containing primary particles of hydroxyapatite and aggregates thereof and granulating the primary particles and the aggregates. A bulk density of the powder is 0.65 g/mL or more and a specific surface area of the secondary particles is 70 m.sup.2/g or more. The powder of the present invention has high strength and is capable of exhibiting superior adsorption capability when it is used for an adsorbent an adsorption apparatus has.

Systems and methods for generation of lime hydrate compounds and particularly highly reactive hydrated lime (HRH) with a reduced resistivity through the inclusion of a sodium compound generally in the slaking water used in generating the lime hydrate or HRH. The compound may then be used in systems which include a Electrostatic Precipitator (ESP) for SO.sub.2 mitigation without many of the associated problems in ESP performance.

An animal litter composition having reduced adhesive properties, and a related method, are disclosed. The animal litter can include a clay-based liquid absorbing material, a filler including one or both of the following: a non-absorbent, non-soluble substrate; an absorbent substrate, and at least one oil present in an amount such that the animal litter composition has a total oil content of about 1.0% by weight to about 7.5% by weight based on the total weight of the animal litter composition.