Embodiments describe a method of depositing an MOF, including depositing a metal solution onto a substrate, spinning the substrate sufficient to spread the metal solution, depositing an organic ligand solution onto the substrate and spinning the substrate sufficient to spread the organic ligand solution and form a MOF layer.

A composition for making composite adsorbents from a mixture of geopolymer, zeolite and activated carbon wherein a geopolymer material, a carbonaceous material, and an alkali activating agent are the components of the mixture. The alkali activating agent to carbonaceous material solid mass ratio is at least 0.25:1, respectively. A process for producing shaped composite adsorbents from the composition is done using conventional means such as mixing, shaping, extrusion and other methods. Alkali activation is used to convert the carbonaceous material to activated carbon, followed by hydrothermal treatment to convert the geopolymer material to zeolites. Shaped composite adsorbents fabricated from the composition of the instant invention are used for adsorption, purification, or other separation applications of liquids and gases.

A method for preparing a modified cellulose aerogel for glycoprotein separation is provided. In this method, cellulose aerogel is employed as a substrate. The cellulose aerogel is known to have a three-dimensional network structure with extremely high porosity and specific surface area and extremely low density. So, by using the cellulose aerogel as a substrate, it is possible to provide the glycoproteins to be separated with more binding sites. PEI dendrimer has abundant functional groups and can easily be modified. By modifying the cellulose aerogel substrate with the PEI dendrimer, it is possible to improve the density of the phenylboronic acid bound to the substrate, thereby leading to higher affinity toward the glycoproteins to be separated.

A preparation method for covalent organic framework 5 (COF-5) includes: adding 2,3,6,7,10,11-hexahydroxytriphenylene and 1,4-phenylenebisboronic acid to a mixed solution of 1,3,5-trimethylbenzene and 1,4-dioxane to form a mixture in the anhydrous and oxygen-free environment; and the addition ratio of 2,3,6,7,10,11-hexahydroxytriphenylene:1,4-phenylenebisboronic acid:1,3,5-trimethylbenzene:1,4-dioxane is 0.02-0.8 mmol:0.08-1.4 mmol:10-15 mL:10-15 mL; sealing the mixture in an airtight container; and obtaining a uniform dispersion solution after shaking the container for wholly mixing the components; heating the dispersion solution to a temperature ranging from 80-100° C.; reacting for a period of time ranging from 72-120 h; and obtaining a precipitate after the reaction; and washing the precipitate, drying the precipitate in vacuum, and heating the precipitate at a temperature ranging from 200-300° C. for a period of time ranging from 1-3 h with a protective atmosphere to obtain COF-5 crystal.

Solid material having an open multiple and at least partially interconnected porosity, comprising an inorganic matrix made of a microporous and mesoporous geopolymer, in which at least partially interconnected open macropores delimited by sides or walls made of microporous and mesoporous geopolymer are defined, and particles of at least one solid compound different from the geopolymer being distributed in the macropores and/or in the sides or walls. Method for preparing said material. Method for separating at least one metal or metalloid cation from a liquid medium containing it, wherein said liquid medium is placed in contact with the material.

A preparation method of charcoal-based fertilizer is provided. Particularly, a special pig manure charcoal modified by amino grafting, a preparation method thereof, and its application in the reuse of nitrogen from farmland drainage are provided. The preparation method includes the following steps: 1) drying raw pig manure to a moisture content of 80%-85% and carrying out pickling, drying, and crushing successively to obtain a dried pig manure powder; 2) conducting liquid nitrogen pretreatment and high-temperature charcoalization to obtain an expanded pig manure charcoal; 3) performing carboxylation treatment to obtain a carboxylated pig manure charcoal; 4) amino grafting: adding an ammonia liquor to the carboxylated pig manure charcoal obtained in step 3), stirring for 20-24 h in an oil bath at 200-240° C.; washing and filtering; and drying and grinding to obtain the special pig manure charcoal modified by amino grafting.

A method for producing a modified sawdust sorbent. The method involves sulfonating sawdust with sulfuric acid and oxidizing the sulfonated sawdust with hydrogen peroxide. The method yields a modified sawdust sorbent containing sulfonated and oxidized cellulose. The modified sawdust sorbent has a higher surface area, higher organic dye adsorption capacity, and more rapid organic dye adsorption rate than unmodified sawdust. A method of using the modified sawdust sorbent for organic dye removal from water is included.

The invention relates to a process for preparing an AFX-structure zeolite comprising at least the following steps: i) mixing, in an aqueous medium, an FAU-structure zeolite having an SiO.sub.2 (FAU)/Al.sub.2O.sub.3 (FAU) molar ratio of between 2.00 (limit included) and 6.00 (limit excluded), an organic nitrogenous compound R, at least one source of at least one alkali and/or alkaline-earth metal M, the reaction mixture having the following molar composition: (SiO.sub.2 (FAU))/(Al.sub.2O.sub.3 (FAU)) between 2.00 (limit included) and 6.00 (limit excluded), H.sub.2O/(SiO.sub.2 (FAU)) between 1 and 100, R/(SiO.sub.2 (FAU)) between 0.01 and 0.6, M.sub.2/nO/(SiO.sub.2 (FAU)) between 0.005 and 0.7, limits included, until a homogeneous precursor gel is obtained; ii) hydrothermal treatment of said precursor gel obtained on conclusion of step i) at a temperature of between 120° C. and 220° C., for a time of between 12 hours and 15 days.

Provided is a porous glass filter obtained by heat-treating alkali borosilicate glass containing an alkali oxide (R.sub.2O), boron trioxide (B.sub.2O.sub.3), and silica (SiO.sub.2) as a composition at a glass transition temperature to phase-separate the alkali borosilicate glass into an alkali boro (R.sub.2O—B.sub.2O.sub.3) phase and silica (SiO.sub.2) phase, and obtained by thermal treatment or acid treatment to dissolve an alkali boro (R.sub.2O—B.sub.2O.sub.3) phase. The manufacturing method includes: a glass forming step of melting and cooling alkali oxide (R.sub.2O), boron trioxide (B.sub.2O.sub.3), and silica (SiO.sub.2) to manufacture an alkali borosilicate glass; a phase separation step of heat-treating the alkali borosilicate glass at a glass transition temperature to phase separation of the alkali borosilicate glass into an alkali borosilicate (R.sub.2O—B.sub.2O.sub.3) phase and a silica (SiO.sub.2) phase; a micropore generation step of generating micropores by the dissolving alkali boro (R.sub.2O—B.sub.2O.sub.3) phase by heat-treating or acid-treating the phase-separated alkali borosilicate glass.

An ion exchange chromatographic packing material is described that includes a copolymer grafted to support resin particles. The copolymer includes an ion exchange group, an ionic crosslinking group configured to ionically bind to the ion exchange group, and an adjustable ionization state group having at least a first net charge at the first pH and a second net charge at the second pH. An overall first net charge of the chromatographic packing material at the first pH is opposite in polarity to the overall second net charge of the chromatographic packing material. This allows impurities to be removed from the chromatographic packing material at the second pH.