Patent classifications
B01J20/28085
NOVEL ORGANIC MATERIAL FOR EXTRACTING THE URANIUM FROM AN AQUEOUS SOLUTION OF PHOSPHORIC ACID, ASSOCIATED METHODS FOR EXTRACTING AND RETRIEVING THE URANIUM AND A PRECURSOR OF SUCH AN ORGANIC MATERIAL
An organic material which includes a solid polymer substrate onto which molecules having the following general formula (I) are grafted:
##STR00001##
The invention also relates to the use of the organic material to extract the uranium (VI) from an aqueous acid solution, to associated methods for extracting and retrieving uranium (VI) as well as to a molecule which is a precursor of the organic material. The disclosure also relates to the use of the organic material to extract the uranium (VI) from an aqueous acid solution, to associated methods for extracting and retrieving uranium (VI) as well as to a molecule which is a precursor of the organic material.
Organic-inorganic hybrid material of use for extracting uranium (VI) from aqueous media containing phosphoric acid, processes for preparing same and uses thereof
The invention relates to an organic-inorganic hybrid material which comprises an inorganic solid support on which are grafted organic molecules of the general formula (I) hereafter: ##STR00001##
and relates to methods allowing preparation of this hybrid material as well as to the uses of the hybrid material for extracting uranium(VI) from an aqueous medium comprising phosphoric acid.
CHROMATOGRAPHIC MATERIALS
In one aspect, the present invention provides a chromatographic stationary phase material for various different modes of chromatography represented by Formula 1: [X](W).sub.a(Q).sub.b(T).sub.c (Formula 1). X can be a high purity chromatographic core composition having a surface comprising a silica core material, metal oxide core material, an inorganic-organic hybrid material or a group of block copolymers thereof. W can be absent and/or can include hydrogen and/or can include a hydroxyl on the surface of X. Q can be a functional group that minimizes retention variation over time (drift) under chromatographic conditions utilizing low water concentrations. T can include one or more hydrophilic, polar, ionizable, and/or charged functional groups that chromatographically interact with the analyte. Additionally, b and c can be positive numbers, with the ratio 0.05?(b/c)?100, and a?0.
PHOSPHATE ADSORBING AGENT FOR BLOOD PROCESSING, BLOOD PROCESSING SYSTEM AND BLOOD PROCESSING METHOD
The present invention relates to a phosphate adsorbing agent for blood processing comprising a porous formed article comprising an organic polymer resin and an inorganic ion adsorbent and having the most frequent pore size of 0.08 to 0.70 ?m measured with a mercury porosimeter. The present invention also relates to a blood processing system and a blood processing method involving the phosphate adsorbing agent for blood processing.
Method for separating meta-xylene using a zeolitic adsorbent with a large external surface area
The invention relates to a method for separating meta-xylene from C8 aromatic fractions, using a zeolitic adsorbent based on sodium-exchanged or sodium-and-lithium-exchanged agglomerated crystals of zeolite Y, with a large external surface area.
Zeolite-based adsorbents based on zeolite X with a low binder content and a low outer surface area, process for preparing them and uses thereof
The invention relates to an adsorbent comprising a zeolite-based phase and a non-zeolite-based phase, said adsorbent having: an outer surface area of less than or equal to 30 m.sup.2.Math.g.sup.1, preferably less than or equal to 20 m.sup.2.Math.g.sup.1, a zeolite-based phase comprising at least one zeolite of FAU structure of X type, and a pore diameter distribution, determined by mercury intrusion according to standard ASTM D 4284-83 and expressed by the volume distribution dV/dlogDHg, in which DHg is the apparent pore diameter and V is the pore volume, the mode of which is between 100 nm and 250 nm, limits inclusive. The invention also relates to a process for preparing the said adsorbent and to the uses thereof, especially for separating xylene isomers.
Co-agglomerated composite materials
A composite filter aid may include diatomaceous earth, natural glass, and a precipitated silica binder, wherein the filter aid has a permeability ranging from 3 to 20 darcys. A composite filter aid may include diatomaceous earth, perlite, and a precipitated silica binder, wherein the filter aid has an alpha density less than 15 lbs/ft.sup.3. A method for making a composite material may include blending diatomaceous earth and perlite, adding alkali silicate to the blended diatomaceous earth and perlite, and precipitating the alkali silicate as a binder to make the composite material. A method for filtering a beverage may include using a composite filter aid and/or composite material.
Sorbent
A method for preparing a sorbent composition includes the steps of: applying, from a solution or a slurry, a layer of a copper compound on the surface of a support material, and drying the coated support material, wherein the thickness of the copper compound layer on the dried support is in the range 1-200 m.
The precursor may be converted to a sorbent suitable for removing heavy metals from liquids or gases by applying one or more sulphur compounds to sulphide the copper compound and form CuS.
Zeolite agglomerates with a halloysite clay binder
A molecular sieve blend containing a zeolite, particularly a zeolite X or A, blended with a halloysite clay binder, wherein the binder contains at least 90% by weight halloysite clay, with a particle length less than about 1 m and processes for the production and use of this blend, particularly for adsorption of water from a feedstream and for the production of oxygen.
Chromatographic materials for the separation of unsaturated molecules
The present disclosure relates to a method of separating a compound of interest, particularly unsaturated compound(s) of interest, from a mixture. The compound is separated using a column having a chromatographic stationary phase material for various different modes of chromatography containing a first substituent and a second substituent. The first substituent minimizes compound retention variation over time under chromatographic conditions. The second substituent chromatographically and selectively retains the compound by incorporating one or more aromatic, polyaromatic, heterocyclic aromatic, or polyheterocyclic aromatic hydrocarbon groups, each group being optionally substituted with an aliphatic group.