The present invention provides a method for performing a purification treatment on a harmful substance-containing liquid, the method enabling an efficient purification treatment of a harmful substance-containing liquid by using dissolved ozone being an oxidizing agent with high level of safety, and a harmful substance-containing liquid purification treatment apparatus for carrying out the method. A method for performing a purification treatment on a harmful substance-containing liquid, the method comprising adding and mixing dissolved ozone into a harmful substance-containing liquid containing a harmful substance, thereafter bringing the harmful substance-containing liquid into contact with a transition metal-containing oxide having a BET specific surface area of 80 m.sup.2/g or more, adsorbing ozone, and adsorbing a harmful substance, and then allowing the harmful substance-containing liquid to flow to accelerate oxidation of the harmful substance by dissolved ozone, thereby performing a highly efficient oxidative decomposition, and a harmful substance-containing liquid purification treatment apparatus for carrying out the method.

A process for producing xylene from C.sub.9+ aromatic hydrocarbons comprises contacting a first feedstock comprising C.sub.9+ aromatic hydrocarbons with a first catalyst in the presence of 0 wt. % or more of hydrogen under effective vapor phase dealkylation conditions to dealkylate part of the C.sub.9+ aromatic hydrocarbons and produce a first product comprising benzene, toluene and residual C.sub.9+ aromatic hydrocarbons. A second feedstock comprising C.sub.9+ aromatic hydrocarbons and benzene and/or toluene is contacted with a second catalyst under effective liquid phase C.sub.9+ transalkylation conditions to transalkylate at least part of the C.sub.9+ aromatic hydrocarbons and produce a second product comprising xylenes.

This invention relates to a hydrogen spillover-based catalyst and use thereof, wherein a hydrogen activation metal cluster is dispersed in the form of being encapsulated in a crystalline or amorphous aluminosilicate matrix which is partially or fully structurally collapsed zeolite, thereby exhibiting high hydroprocessing or dehydrogenation activity and suppressed CC hydrogenolysis activity.

An aluminosilicate molecular sieve of AFT framework type, designated SSZ-112, is provided. SSZ-112 is synthesized using a mixed-template method. SSZ-112 may be used in catalytic and sorptive processes.

Provided is a NaY molecular sieve and a method for preparing the NaY molecular sieve, an HY molecular sieve and a method for preparing the HY molecular sieve, a hydrocracking catalyst, and a hydrocracking method. The average grain diameter of the NaY molecular sieve is 2-5 m, and the sum of pore volumes of pores in 1-10 nm diameter accounts for 70-90% of the total pore volume of the NaY molecular sieve. The HY molecular sieve obtained from the large-grain NaY molecular sieve can be used as an acidic component in the hydrocracking catalyst. When the hydrocracking catalyst containing the HY molecular sieve is applied in the hydrocracking reaction of heavy oils that contain macromolecules, it can provide better cracking activity and product selectivity in the hydrocracking reaction.

A catalyst structure includes a porous support structure, where the support structure includes an aluminosilicate material and any two or more metals loaded in the porous support structure selected from Ga, Ag, Mo, Zn, Co and Ce. The catalyst structure is used in a hydrocarbon upgrading process that is conducted in the presence of methane, nitrogen or hydrogen.

A catalyst structure includes a porous support structure, where the support structure includes an aluminosilicate material and any two or more metals loaded in the porous support structure selected from Ga, Ag, Mo, Zn, Co and Ce. The catalyst structure is used in a hydrocarbon upgrading process that is conducted in the presence of methane, nitrogen or hydrogen.

A cluster-supporting catalyst including porous carrier particles having acid sites, and catalyst metal clusters supported within the pores of the porous carrier particles. In the cluster-supporting catalyst including porous carrier particles having acid sites, and catalyst metal clusters supported within the pores of the porous carrier particles, the catalyst metal may be rhodium, the catalyst metal may be palladium, the catalyst metal may be platinum, or the catalyst metal may be copper.

This invention relates to a hydrogen spillover-based catalyst and use thereof, wherein a hydrogen activation metal cluster is dispersed in the form of being encapsulated in a crystalline or amorphous aluminosilicate matrix which is partially or fully structurally collapsed zeolite, thereby exhibiting high hydroprocessing or dehydrogenation activity and suppressed C-C hydrogenolysis activity.

The present invention concerns a process for forming a primary or a secondary amine via amination reaction comprising: reacting an alcohol with an amine in the presence of a zeolite comprising a transition metal chosen in the group consisting of Group 8 to 12 elements of the Periodic Table and any combination thereof.