The present invention provides a particulate cobalt ion adsorbent which has a high adsorption capacity. A particulate cobalt ion adsorbent which contains potassium hydrogen dititanate hydrate represented by chemical formula K.sub.2-XH.sub.xO.2TiO.sub.2.nH.sub.2O (wherein x is 0.5 or more and 1.3 or less, and n is greater than 0), and no binder, wherein the particulate cobalt ion adsorbent has a particle size range of 150 μm or more and 1000 μm or less.

Proposed is an inorganic ion-exchanger, which is selective to lithium and constituted a non-stoichiometric compound in the form of solid particles of a polymeric aqua-oxo-hydroxo complex represented by the following general formula: H.sub.aNbO.sub.(2.5+0.5.Math.a).cZrO.sub.2.dH.sub.2O, wherein: “a” is a number ranging from 0.5 to 1.5, “c” is a number ranging from 0.01 to 1.0, and “d” is a number ranging from 0.1 to 2.0. The complex has a total ion exchange capacity of at least 3.5 meq/g and an ion-exchange capacity specifically to lithium of at least 2.5 meq/g. This ion-exchanger is intended for selective extraction of lithium from lithium-containing natural and industrial brines.

Disclosed herein is a continuous process for preparing zeolitic material with a CHA-type framework structure comprising SiO.sub.2 and X.sub.2O.sub.3 and the zeolitic material so-obtained. The processes comprises (i) preparing a mixture comprising one or more sources of SiO.sub.2, one or more sources of X.sub.2O.sub.3, seed crystals, one or more tetraalkylammonium cation R.sup.5R.sup.6R.sup.7R.sup.8N+-containing compounds as structure directing agent, and a liquid solvent system; (ii) continuously feeding the mixture prepared in (i) into a continuous flow reactor at a liquid hourly space velocity; and (iii) crystallizing the zeolitic material with a CHA-type framework structure from the mixture in the continuous flow reactor.

Disclosed herein is a continuous process for preparing zeolitic material with a CHA-type framework structure comprising SiO.sub.2 and X.sub.2O.sub.3 and the zeolitic material so-obtained. The processes comprises (i) preparing a mixture comprising one or more sources of SiO.sub.2, one or more sources of X.sub.2O.sub.3, seed crystals, one or more tetraalkylammonium cation R.sup.5R.sup.6R.sup.7R.sup.8N+-containing compounds as structure directing agent, and a liquid solvent system; (ii) continuously feeding the mixture prepared in (i) into a continuous flow reactor at a liquid hourly space velocity; and (iii) crystallizing the zeolitic material with a CHA-type framework structure from the mixture in the continuous flow reactor.

Methods are disclosed for achieving the catalytic combustion of a gaseous species in low temperature humid environments. The methods comprise the steps of obtaining a combustion catalyst composition comprising an amount of a precious metal supported on an ion-exchangeable alkali metal titanate substrate, and then exposing the species to the combustion catalyst composition in the presence of an oxygen containing gas and water vapour at a catalysis temperature below 200° C. and at a relative humidity above 0.5%. A novel desiccant-coupled catalytic combustion process and system are also disclosed.

A method of producing ammonium phosphates from at least one mineral containing phosphate and an element which is calcium, magnesium, iron, or aluminum. The method includes contacting the at least one mineral (or a combination of them) with a cation exchanger for a time and at a temperature sufficient to yield phosphoric acid from the mineral.

The invention relates to a process for performing a aqueous synthesis of titanium phosphates (TiP) having solely —H2PO4 groups, which process is characterised by the following steps: providing titanium (IV) oxysulphate, TiOSO4, in an aqueous solution or in a powder and H2SO4, substantially without transition divalent metal ions, including cobalt (II) and copper (II), heating N of the thus formed aqueous solution to above 50° C., but below 85° C. for at least 30 minutes, providing a controlled amount of H3PO4 to said aqueous solution, to form an aqueous solution containing a molar ratio between TIO2 and P2Os being controlled to about 1:1, pot not above 1:1.5 and not below 1:0.7, stirring the thus formed aqueous solution for at least 3 hours to form precipitates of titanium Got phosphate, and allowing ageing of said solution, without stirring, acidic washing of the formed precipitate using HCl or other acids to obtain TiO(OH)(H2PO4)-H2O having solely —H2PO4 ion-exchange chemical groups and allowing said precipitates to dry to a powder product, substituting protons in the powder product TiO(OH)(H2PO4)-H2O to sodium cations by treatment of the latter with solutions of sodium carbonate and allowing the thus formed powder of Na—TiP1 to dry.

The invention relates to a process for performing a aqueous synthesis of titanium phosphates (TiP) having solely —H2PO4 groups, which process is characterised by the following steps: providing titanium (IV) oxysulphate, TiOSO4, in an aqueous solution or in a powder and H2SO4, substantially without transition divalent metal ions, including cobalt (II) and copper (II), heating N of the thus formed aqueous solution to above 50° C., but below 85° C. for at least 30 minutes, providing a controlled amount of H3PO4 to said aqueous solution, to form an aqueous solution containing a molar ratio between TIO2 and P2Os being controlled to about 1:1, pot not above 1:1.5 and not below 1:0.7, stirring the thus formed aqueous solution for at least 3 hours to form precipitates of titanium Got phosphate, and allowing ageing of said solution, without stirring, acidic washing of the formed precipitate using HCl or other acids to obtain TiO(OH)(H2PO4)-H2O having solely —H2PO4 ion-exchange chemical groups and allowing said precipitates to dry to a powder product, substituting protons in the powder product TiO(OH)(H2PO4)-H2O to sodium cations by treatment of the latter with solutions of sodium carbonate and allowing the thus formed powder of Na—TiP1 to dry.

The invention relates to a new use of spun, continuous inorganic fibers having a diameter smaller than 1 μm in the form of monolithic structures with at least one dimension equal to or greater than about 50 μm. The monolithic structures are formed by self-entanglement of the continuous fibers as an ion exchange material. In particular the invention relates to a new ion exchange material bed comprising such fibers and ion exchange unit comprising such bed. The invention improves the efficiency and sustainability of ion exchangers.

The invention relates to a new use of spun, continuous inorganic fibers having a diameter smaller than 1 μm in the form of monolithic structures with at least one dimension equal to or greater than about 50 μm. The monolithic structures are formed by self-entanglement of the continuous fibers as an ion exchange material. In particular the invention relates to a new ion exchange material bed comprising such fibers and ion exchange unit comprising such bed. The invention improves the efficiency and sustainability of ion exchangers.