The present invention relates to an improved diatomaceous earth composition containing salt water. The diatomaceous earth composition according to the present invention comprises an agglomerated mixture of calcined diatomaceous earth particles, water and at least one inorganic salt, wherein the mass ratio of the calcined diatomaceous earth particles and water is in the range of 1:1.0 to 1:2.0, and wherein the content of the at least one inorganic salt is equal to or more than 0.25 parts by mass based on 100 parts by mass of water. In a further aspect, the present invention relates to a method for producing the diatomaceous earth composition according to the present invention. In another aspect, the present invention relates to the use of the diatomaceous earth composition according to the present invention as an agent for precoat filtration or dynamic body feed filtration in biopharmaceutical applications.

[Problem] In an embodiment involving addition of a chelating agent in an upstream process of the process for production, such as the polymerization step, the residual ratio of the chelating agent in the final product, a particulate water-absorbing agent, is improved.

[Solution] A particulate water-absorbing agent having a poly(meth)acrylic acid (salt)-based water-absorbing resin as a main component, containing a chelating agent having a nitrogen atom and an inorganic reducing agent having a sulfur atom, wherein the particulate water-absorbing agent has a chelating agent ratio of 0.8 to 1.8, as calculated by the following procedures (a) to (c): (a) subjecting the particulate water-absorbing agent to a predetermined impact test; (b) sieving the particulate water-absorbing agent subjected to the impact test into a particle group 1 with a particle size of less than 300 μm and a particle group 2 with a particle size of 300 μm or more and less than 850 μm using a JIS standard sieve; and (c) quantifying a content C1 of the chelating agent present in the particle group 1 and a content C2 of the chelating agent present in the particle group 2, and then dividing the C1 by the C2.

A method for forming an amine-functionalized solid CO.sub.2 sorbent for carbon capture may include providing a support material and applying at least one cycle of molecular layer deposition (MLD) with an amine precursor onto the surface of the support material. An amine layer formed on the support material contains amine groups/amine-containing ligands to adsorb CO.sub.2 onto the support material in a low temperature operating window for adsorption and desorption without the loss of active sites.

A composite that includes graphene and an interfacially-polymerized polyamide, where the composite is in the form of a self-supporting membrane having a graphene side opposite to a polyamide side, or the composite is in the form of a microparticle comprising a graphene core and a polyamide shell, a method of manufacture of the composites by interfacial polymerization and methods of use of the composite are described.

A method of removing one or more antibiotics from a dairy product, the method involve passing the dairy product comprising an antibiotic in a first amount through a bulk comprising, relative to a total bulk weight, at least 75 wt. % of titanium oxide nanostructures, to provide the dairy product comprising the antibiotic in a second, lesser amount, wherein the nanostructures have lengths at least two-fold in excess of their width and height. Bulk materials useful in this or related methods or applications may have loosely tangled, noodle-like morphologies on sub-100 nm scale, and need not employ graphene and/or polymeric support networks in columns, generally having only titanium oxides without silicon or iron oxides.

A method for preparing a modified sodium fluoride adsorbent includes the following steps: S1. producing spherical particles of NiCl.sub.12.6H.sub.2O and porous NaF with a mass ratio of 1:3.0-3.5; S2. sintering the spherical particles in a vacuum environment at a temperature of 120-130° C. for 10-40 hours and at a temperature of 280-300° C. for 10-40 hours, respectively, to form an adsorbent intermediate with a NiCl.sub.2—NaF framework, wherein, a vacuum degree is less than or equal to 500 pa; and S3. treating the adsorbent intermediate by fluorine-nitrogen mixtures with high purity to obtain the novel sodium fluoride adsorbent having NiCl.sub.2—NaF framework. The modified sodium fluoride adsorbent can effectively separate chlorine trifluoride and hydrogen fluoride molecules, and the optimal adsorption rate of hydrogen fluoride is upgraded to more than 98%. While, the optimal adsorption rate of chlorine trifluoride is lowered down to around 3%.

An alumina grain has a single-crystal structure and has an approximate regular octahedral stereoscopic morphology. Eight sides of the alumina grain belong to the {111} family of crystal planes of γ-state alumina, and the grain size is 5-100 μm. The alumina grain is unique in crystal plane exposure and distribution, simple and feasible in preparation, and low in cost, and has higher operability, and thus has good application prospect in the field of catalysis and adsorption.

An apparatus, system, and method for removing impurities from a non-aqueous electrolyte used in an electrochemical cell. The apparatus includes a vessel having one or more chambers with an inlet and an outlet configured to allow the flow of the electrolyte through the one or more chambers; and an inorganic scavenging agent located within the one or more chambers. The inorganic scavenging agent includes one or more types of zeolite particles, at least one type of absorbent filler particles, or a combination of the zeolite and absorbent filler particles. The inorganic scavenging agent absorbs one or more of moisture, free transition metal ions, or hydrogen fluoride (HF) that is present as impurities in the non-aqueous electrolyte.

The present technology provides an adsorbent material that includes a silicate composition, wherein the silicate composition includes a crystalline phase; wherein the silicate composition may have an interconnected porous scaffold having a total mercury (Hg) pore volume of about 0.005 cc/g to about 0.25 cc/g for pores having a diameter of about 20-10,000 Å and a total nitrogen (N) pore volume of about 0.02 cc/g to about 0.1 cc/g for pores having a diameter of about 20-600 Å.

The present invention relates yolk-shell nanoparticles having both a high stability towards sintering and high H.sub.25 adsorption capacities, the use of the yolk-shell nanoparticles in a method for H.sub.2S removal from gas streams, and a corresponding method for H.sub.2S removal from gas streams also comprising the regeneration of the yolk-shell nanoparticles, wherein the yolk-shell nanoparticles provide for high H.sub.2 adsorption capacities and/or high reusability.