A filtration material including a silica base material having a group represented by the following general formula (a0-1) [in formula (a0-1), Ya.sup.01 represents a divalent linking group; Ra.sup.01 represents a hydrocarbon group which may have a substituent; Ra.sup.02 represents a hydroxyl group or a hydrocarbon group having 1 to 6 carbon atoms which may have a substituent; n.sup.01 represents an integer of 0 to 5; and the symbol “*” represents a valence bond with respect to the silica base material].

##STR00001##

A method of making absorbent granules can include mixing activated carbon with a liquid and a binder to form a slurry; applying the slurry to particles of absorbent core material to at least partially coat the particles of the core material with a first distinct layer containing the activated carbon; and applying a clumping agent to the first distinct layer to at least partially coat the first distinct layer with a second distinct layer containing the clumping agent. The absorbent granules can be used as a deodorizer and/or a pet litter, and each of the absorbent granules can include an absorbent core, a first distinct layer containing activated carbon, and a second distinct layer containing a clumping agent such that the first distinct layer is between an outer surface of the absorbent core and an inner surface of the second distinct layer.

Composite materials and methods of preparing C0.sub.2 capture include: (1) a porous solid support comprising a plurality of porous channels; and (2) a nucleophilic source associated with the porous channels of the porous solid support. The nucleophilic source is capable of converting the captured C0.sub.2 to poly(C0.sub.2). Methods of capturing C0.sub.2 from an environment include associating the environment with the aforementioned composite materials to lead to the capture of C0.sub.2 from the environment. Such methods may also include a step of releasing the captured C0.sub.2 from the composite material. The associating step comprises a conversion of the captured C0.sub.2 to poly(C0.sub.2) in the composite material. A releasing step may also include a depolymerization of the formed poly(C0.sub.2).

The present invention relates to a calcined diatomite aggregate coated with metal oxides, more specifically to a diatomite aggregate having a diameter larger than 2 mm.

A carbon dioxide adsorbent including silica gel and an amine compound carried by the silica gel. The silica gel has a spherical shape, a particle size ranging from 1 mm to 5 mm inclusive, an average pore diameter ranging from 10 nm to 100 nm inclusive, a pore volume ranging from 0.1 cm.sup.3/g to 1.3 cm.sup.3/g inclusive, and a waterproof property N that is defined by an expression (1) and that is not lower than 45%,

N=(W/W.sub.0)×100  (1) where N is the waterproof property in percentage (%) of the silica gel, W.sub.0 is a total number of particles of the silica gel immersed in water, W is a number of particles of the silica gel not subjected to breakage out of W.sub.0.

The invention discloses a core-shell structure polymer magnetic nanosphere with a high Cr (VI) adsorption capacity and its preparation method and application. The preparation method includes: adding Fe.sub.3O.sub.4 powder into a mixed solution of water and ethanol, dispersing Fe.sub.3O.sub.4 powder in the solution evenly by ultrasound, sequentially adding resorcinol and formaldehyde into the suspension to adjust a pH, stirring and reacting to obtain Fe.sub.3O.sub.4@RF evenly dispersed in a chitosan solution, dropwise adding the prepared suspension into a mixed solution of paraffin and span 80, stirring for a period of time, adding a glutaraldehyde aqueous solution, stirring and reacting to obtain a magnetic chitosan nanosphere. The magnetic chitosan nanosphere prepared may be applied to adsorbing Cr (VI) in a water solution. Not only the magnetic chitosan nanospheres prepared has a high adsorption capacity for Cr (VI), but also can be quickly separated by an external magnetic field after adsorption.

The present disclosure discloses a carbon capture material prepared by needle-tube microfluidics and a preparation method thereof. The carbon capture material includes a sorbent and a microencapsulating shell, the sorbent includes one of an aqueous potassium carbonate solution or an aqueous ethanolamine solution or an aqueous ethanolamine solution containing graphene sheets, and the aqueous potassium carbonate solution or the aqueous ethanolamine solution or the aqueous ethanolamine solution containing graphene sheets is prepared by a microfluidic device. In the present disclosure, one of the aqueous potassium carbonate solution or the aqueous ethanolamine solution or the aqueous ethanolamine solution containing graphene sheets is used as a sorbent to prepare carbon capture particles by the microfluidic technology for the first time.

The present disclosure provides a preparation method of AM-type polystyrene microsphere ofloxacin imprinted polymer as well as an application thereof. A monomer acrylamide and an initiator ammonium persulfate are subjected to graft polymerization on the surface of modified polystyrene primary amine resin, to get grafted particles; then an adsorption test of a levofloxacin solution by the grafted particles PAM/PSA is conducted, and then a levofloxacin surface molecularly imprinted material MIP-PAM/PSA is prepared by using ethylene glycol diglycidyl ether as the crosslinking agent. The present disclosure can realize the separation and purification of racemic ofloxacin effectively, thus providing a new method and material for separating and enriching s-type ofloxacin in the industry. Because the antibacterial efficacy of S-ofloxacin on Gram-negative bacteria and positive bacteria is 8-128 times that of its enantiomer R-ofloxacin, so the present technology can improve the efficacy of a drug greatly.

The present disclosure relates to methods for producing metal sulfide disposed on particle substrates. In at least one embodiment, a method for producing an alkali earth hydroxide particle having a metal sulfide disposed thereon includes introducing an alkali earth oxide particle with a metal sulfate to form a first composition. The method includes introducing an alkali sulfide or an alkali earth sulfide with the first composition to form a second composition. The present disclosure further relates to compositions of matter having metal sulfide disposed on a particle substrate. In at least one embodiment, a composition of matter includes an alkali earth hydroxide particle. The composition of matter includes a metal sulfide disposed on the alkali earth hydroxide particle.

Functionalized material, methods of producing the functionalized material, and use thereof for separation processes such as for separating and extracting a dissolved organic foulant, charged contaminant or oily matter or any combination thereof from water (e.g., produced water), are provided. The method of making the functionalized material, can include: a) providing a mineral material; b) providing an alkyl chain and/or a perfluorinated species, the alkyl chain or perfluorinated species selected to dissolve organic foulants, charged contaminants or oily matter from water or any combination thereof; c) hydroxylating the material via a concentrated acid solution or a basic solution; and d) grafting the alkyl chain and/or the perfluorinated species onto the material via a silanation reaction.