The invention refers to the process of obtaining porous spheres based on CaO modified with carbon nanotubes for the capture of CO.sub.2. The invention also refers to the spheres obtained and their use to capture CO.sub.2 generated by a vehicular internal combustion engine, aiming to reduce the amount of CO.sub.2 released into the atmosphere.

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.

The present invention relates to a process for the production of a zeolitic material having an MWW framework structure comprising YO.sub.2 and B.sub.2O.sub.3, wherein Y stands for a tetravalent element, said process comprising (i) preparing a mixture comprising one or more sources for YO.sub.2, one or more sources for B.sub.2O.sub.3, one or more organotemplates, and seed crystals, (ii) crystallizing the mixture obtained in (i) for obtaining a layered precursor of the MWW framework structure, (iii) calcining the layered precursor obtained in (ii) for obtaining the zeolitic material having an MWW framework structure, wherein the one or more organotemplates have the formula (I)

R.sup.1R.sup.2R.sup.3N   (I) wherein R.sup.1 is (C.sub.5-C.sub.8)cycloalkyl, and wherein R.sup.2 and R.sup.3 are independently from each other H or alkyl, and wherein the mixture prepared in (i) and crystallized in (ii) contains 35 wt.-% or less of H.sub.2O based on 100 wt.-% of YO.sub.2 contained in the mixture prepared in (i) and crystallized in (ii), as well as to a synthetic boron-containing zeolite which is obtainable and/or obtained according to the inventive process and to its use.

Described herein is a process for producing a zeolitic material having an MWW framework structure containing YO.sub.2 and B.sub.2O.sub.3, in which Y stands for a tetravalent element. The process includes the steps of (i) preparing a mixture containing one or more sources for YO.sub.2, one or more sources for B.sub.2O.sub.3, one or more organotemplates, and seed crystals, (ii) crystallizing the mixture obtained in (i) for obtaining a layered precursor of the MWW framework structure, and (iii) calcining the layered precursor obtained in (ii) for obtaining the zeolitic material having an MWW framework structure. Also disclosed herein are synthetic boron-containing zeolites obtain by the process and uses thereof.

Methods of preparing organosilica materials using a starting material mixture comprising at least one compound of Formula [(RO).sub.2SiCH.sub.2].sub.3 (Ia) and at least one compound of Formula [R′ROSiCH.sub.2].sub.3 (Ib), wherein each R′ independently represents an RO—, an R group, or an (RO).sub.3Si—CH.sub.2— group, at least one R′ being (RO).sub.3Si—CH.sub.2—; and R represents a C.sub.1-C.sub.4 alkyl group, in the absence of a structure directing agent and/or porogen are provided herein. Processes of using the organosilica materials, e.g., for gas separation, etc., are also provided herein.

The present invention relates to a carbon sorbent the can selectively remove platinum-group metals and other heavy metals such as tin without co-removing organic synthesis products including pharmaceutical intermediates and finished Active Pharmaceutical Ingredients (APIs). The carbon sorbents of the present invention are made from low-cost, high purity starting materials and the resulting carbon sorbents are also very pure. The carbon sorbents possess a combination of certain nitrogen and phosphorous groups combined with mesoporosity (2 to 50 nm diameter pores) that proves the high metal adsorption.

A method for manufacturing a diatomaceous earth functional filler product with detectable or non-detectable crystalline silica includes the steps of: selecting a diatomaceous earth ore; simultaneously milling and flash-drying the diatomaceous earth ore; beneficiating the milled and flash-dried diamtomaceous earth ore; blending the beneficiated diatomaceous earth ore with a fluxing agent; calcining the blended diatomaceous earth ore and fluxing agent to produce an initial diatomaceous earth powder; air-classifying the initial diatomaceous earth powder to produce a first fraction including the diatomaceous earth functional filler product and a second fraction including coarse particles; further milling the coarse particles to produce additional diatomaceous earth powder; and re-circulating the additional diatomaceous earth powder to blend the additional diatomaceous earth powder with the initial diatomaceous earth powder.

Provided are superabsorbent materials composed of one or more water-soluble polysaccharides, such as gelling polysaccharides and gelling-compatible polysaccharides, and one or more insoluble fibers. The disclosed superabsorbent materials have a porous network structure and highly stable gelling properties as well as high absorption ratio and volume expansion capacity upon hydration or rehydration. Also provided are methods for preparing such superabsorbent materials and uses thereof.

Provided are superabsorbent materials composed of one or more water-soluble polysaccharides, such as gelling polysaccharides and gelling-compatible polysaccharides, and one or more insoluble fibers. The disclosed superabsorbent materials have a porous network structure and highly stable gelling properties as well as high absorption ratio and volume expansion capacity upon hydration or rehydration. Also provided are methods for preparing such superabsorbent materials and uses thereof.

Provided are superabsorbent materials composed of one or more water-soluble polysaccharides, such as gelling polysaccharides and gelling-compatible polysaccharides, and one or more insoluble fibers. The disclosed superabsorbent materials have a porous network structure and highly stable gelling properties as well as high absorption ratio and volume expansion capacity upon hydration or rehydration. Also provided are methods for preparing such superabsorbent materials and uses thereof.