To provide a hydrocarbon reforming/trapping material which is capable of adsorbing and reforming a hydrocarbon. A hydrocarbon reforming/trapping material of the present invention has an SiO.sub.2/Al2O.sub.3 ratio of from 7 to 12, and contains an Fe(II)-substituted beta zeolite which is ion-exchanged by Fe(II) ions. The amount of supported Fe(II) is preferably 0.001-0.5 mmol/g with respect to the Fe(II)-substituted beta zeolite. This Fe(II)-substituted beta zeolite is suitably produced by dispersing and mixing a beta zeolite having an SiO.sub.2/Al.sub.2O.sub.3 ratio of from 7 to 12 in an aqueous solution of a water-soluble compound of divalent iron, and mixing and stirring the solution, so that Fe(II) ions are supported on the beta zeolite.

A method for separating at least one hydrocarbon from a feed containing a mixture of at least one hydrocarbon and nitrogen, comprising contacting the feed with an adsorbent comprising a porous support wherein the porous support comprises exchangeable cations and at least a portion of the exchangeable cations are organic cations.

The technology disclosed herein is directed to controlling humidity levels, such as the humidity level in an enclosed environment. The water isotherm of the adsorbent material is customized through the modification of the surface chemistry of the adsorbent. By modifying the surface chemistry of the adsorbent in various ways and to varying degrees, it is possible to customize the adsorbent properties to a range of different humidity levels. Such modification can enhance the adsorbing capacity and efficiency of the adsorbent, especially with regard to low molecular weight water-soluble compounds.

The present disclosure is directed to a potassium-form MER framework type zeolite, a MER framework type zeolite having a stick-like morphology, wherein the potassium is present as K.sup.+ in extra-framework locations. The zeolite is essentially free of an extra-framework cation other than potassium.

An active package having LTA zeolites exchanged with palladium is described. This solution is capable to improve the quality of the gaseous atmosphere within the package itself, with particular reference to the presence of ethylene. This solution provides improved performance when the package is accidentally exposed to hydrocarbon vapors and provides benefits in terms of reliability in the ethylene control.

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/d log DHg, 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.

The present invention relates to a zeolite-based adsorbent comprising at least one zeolite of FAU structure of LSX type and comprising barium and/or potassium, in which the outer surface area of said zeolite-based adsorbent, measured by nitrogen adsorption, is between 20 m.sup.2.Math.g.sup.−1 and 100 m.sup.2.Math.g.sup.−1, limits inclusive. The present invention also relates to the use of such a zeolite-based adsorbent as an adsorption agent, and also to the process for separating para-xylene from aromatic isomer fractions containing 8 carbon atoms.

Provided is a surfactant-free, single-step synthesis of delaminated aluminosilicate zeolites. The process comprises the step of heating a borosilicate zeolite precursor in a metal salt solution, e.g., an aluminum nitrate solution, zinc nitrate solution or manganese nitrate solution. The delaminated aluminosilicate zeolite product is then recovered from the solution.

A separation membrane structure comprises a porous support, a first separation membrane formed on the porous support, and a second separation membrane formed on the first separation membrane. The first separation membrane has an average pore diameter of greater than or equal to 0.32 nm and less than or equal to 0.44 nm. The second separation membrane includes addition of at least one of a metal cation or a metal complex that tends to adsorb nitrogen in comparison to methane.

A separation membrane structure comprises a porous suppor, and a separation membrane formed on the porous support. The separation membrane has an average pore diameter of greater than or equal to 0.32 nm and less than or equal to 0.44 nm. The separation membrane includes addition of at least one of a metal cation or a metal complex that tends to adsorb nitrogen in comparison to methane.