A mesosilicalite nanocarrier having a hierarchical silicalite characterized by a molar ratio of aluminum to silica in a range of 1:3000 to 1:1000. The hierarchical silicalite includes mesopores of a hexagonal structure, and micropores of silicalite structure with a microporous volume in the range of 0.05 cc/g to 0.1 cc/g. The nanocarrier has a mesophase content in the range of 30 wt % to 70 wt %, a microphase content in the range of 30 wt % to 70 wt %, and a mean pore diameter in the range of 1.5 nm to 5.5 nm. A method of preparing the stable mesosilicalite nanocarrier with hierarchical micro/mesopores to load an antioxidant or drug for targeted drug delivery is also described.

According to one or more embodiments presently disclosed, one or more reactant hydrocarbons may be dehydrogenated by a method that includes contacting the one or more reactant hydrocarbons with a catalyst system to dehydrogenate at least a portion of the reactant hydrocarbons. The catalyst system may include a zincosilicate support material that includes an MFI framework type structure incorporating at least silicon and zinc. The catalyst system may further include one or more alkali or alkaline earth metals, and one or more platinum group metals.

Provided is a method capable of easily producing a layered silicate in a short time. The problem may be solved by a method of producing a layered silicate, including the following steps (a) and (b): (a) providing a cage silicate that contains an anion component represented by formula (1) below and a cation component represented by formula (2) below with a ratio of the mole number of water to the mole number of the anion component in terms of SiO.sub.2, (H.sub.2O/SiO.sub.2), of 0.7 to 30;

##STR00001## (in formula (2), R represents an alkyl group having 2 to 9 carbon atoms) and (b) treating the cage silicate obtained in step (a) in an autoclave.

A process comprising hydrothermally synthesizing a titanium-containing zeolitic material having framework type MWW in the presence of an MWW template compound, obtaining a mother liquor comprising water, a first portion of the MWW template compound and a titanium-containing zeolitic material having framework type MWW comprising a second portion of the MWW template compound, separating the first portion of the MWW template compound from the mother liquor and recycling the first portion of the MWW template compound into a hydrothermal synthesis of a titanium-containing zeolitic material having framework type MWW.

The present invention refers to a microporous crystalline material, to the method for the production thereof and to the use of same, the material having a composition:
xX.sub.2O.sub.3:zZO.sub.2:yYO.sub.2
in which: X is a trivalent element such as Al, B, Fe, In, Ga, Cr, or mixtures thereof, where (y+z)/x can have values of between 9 and infinity; Z corresponds to a tetravalent element selected from Si, Ge or mixtures thereof; and Y corresponds to a tetravalent element such as Ti, Sn, Zr, V or mixtures thereof, where z/y can have values of between 10 and infinity.

The present disclosure relates to catalyst systems which may be useful for the dehydrogenation of hydrocarbons. According to one or more embodiments, the catalyst systems may include a zincosilicate support material, one or more alkali or alkaline earth metals, and one or more platinum group metals. The zincosilicate support material may include an MFI framework type structure incorporating at least silicon and zinc. The present disclosure also relates to methods for the production of such catalyst systems as well as methods for the use of such catalyst systems for the dehydration of hydrocarbons.

The present invention provides a titanosilicate separation membrane which can also be used for separating a mixed gas containing a molecule having a relatively small size, has high durability in a high temperature environment, and has a high permeation rate and a high selectivity for a mixed gas containing water vapor. A titanosilicate separation membrane has a CHA-type titanosilicate crystal structure formed on a porous support, wherein aluminum is not substantially contained in the backbone of the titanosilicate crystal structure, and the titanosilicate crystal structure is constituted by silicon, oxygen, and titanium.

The present disclosure relates to catalyst systems which may be useful for the dehydrogenation of hydrocarbons. According to one or more embodiments, the catalyst systems may include a zincosilicate support material, one or more alkali or alkaline earth metals, and one or more platinum group metals. The zincosilicate support material may include an MFI framework type structure incorporating at least silicon and zinc. The present disclosure also relates to methods for the production of such catalyst systems as well as methods for the use of such catalyst systems for the dehydration of hydrocarbons.

According to one or more embodiments presently disclosed, one or more reactant hydrocarbons may be dehydrogenated by a method that includes contacting the one or more reactant hydrocarbons with a catalyst system to dehydrogenate at least a portion of the reactant hydrocarbons. The catalyst system may include a zincosilicate support material that includes an MFI framework type structure incorporating at least silicon and zinc. The catalyst system may further include one or more alkali or alkaline earth metals, and one or more platinum group metals.

According to one or more embodiments presently disclosed, a catalyst system may be made by a method that includes introducing one or more alkali or alkaline earth metals to a zincosilicate support material, and introducing one or more platinum group metals to the zincosilicate support material. The zincosilicate support material may include an MFI framework type structure incorporating at least silicon and zinc.