Processes for conversion of methane and ethane into syngas and ethylene are provided. An exemplary process can include providing a reaction mixture of methane, ethane, oxygen, and carbon dioxide and contacting the reaction mixture with a catalyst that includes at least one metal oxide. The processes can be combined processes in which oxidative dry reforming of methane and dehydrogenation of ethane to ethylene with carbon dioxide and oxygen occur concurrently.

The invention relates to an oligomerization catalyst comprising nickel oxide and silica-alumina support material and to a process for oligomerization of C3- to C6-olefins using the oligomerization catalyst.

Oligomerization of C.sub.3- to C.sub.5-olefins using a catalyst is inhibited, wherein the oligomerization is carried out in at least one reaction stage including at least one reactor and at least one distillation column, and wherein the oligomer content in the feed stream to the at least one reactor of the at least one reaction stage is at least 1% by weight.

A process for the production of oligomerized olefins comprising the following steps: purification of an organic composition (OC1) in at least one adsorber to obtain an organic composition (OC2); oligomerization of organic composition (OC2) in the presence of a catalyst to obtain an organic composition (OC3); distillation of organic composition (OC3) in a distillation column (D1) to obtain an organic composition (OC4) from the upper part of (D1) and an organic composition (OC5) from the lower part of (D1); hydrogenation of organic composition (OC4) to obtain an organic composition (OC1 1) and regeneration of an adsorber (A1) employing organic composition (OC11) as regeneration media.

A method of implementing organic synthesis reactions uses a composition containing a metal catalyst originating from a calcined plant. The plants can be from the Brassicaceae, Sapotaceae and Convolvulaceae family, and the metal catalyst contains metal in the M(II) form such as zinc, nickel, manganese, lead, cadmium, calcium, magnesium or copper. Examples of the organic synthesis reactions include halogenations, electrophilic reactions, cycloadditions, transesterification reactions and coupling reactions, among others.

The invention relates to polyoxometalates represented by the formula (A.sub.n).sup.m+[M′M.sub.12X.sub.8O.sub.yR.sub.zH.sub.q].sup.m− or solvates thereof, corresponding supported polyoxometalates, and processes for their preparation, as well as corresponding metal clusters, optionally in the form of a dispersion in a liquid carrier medium or immobilized on a solid support, and processes for their preparation, as well as their use in reductive conversion of organic substrate.

Disclosed are a molybdenum based composite oxide catalyst, its preparation method and use. The catalyst has the following general formula: BiMo.sub.xM.sub.yN.sub.zO.sub.a; wherein M is one of V, Cr, Mn, Fe, Co, Ni and Cu, or a mixture of two or more of V, Cr, Mn, Fe, Co, Ni and Cu in any ratio; N is one of Na, K, Cs, Ca and Ba, or a mixture of two or more of Na, K, Cs, Ca and Ba in any ratio; x=0.5˜20; y=0.05˜20; z=0.01˜5; a is a number satisfying the valance of each atom. The catalyst is prepared by the following method: firstly mixing a certain amount of the lead metal oxides according to the chemical proportion and then grinding the mixture with high-energy ball milling for a period of time to obtain the molybdenum based composite oxide catalyst. The catalyst exhibits excellent performance when using for preparation of butadiene by oxidative dehydrogenation of butene, and the preparation process is simple, controllable, and repeatable. Waste water or waste gas that is difficult to be treated is not produced during preparation.

The present disclosure discloses a multistage nanoreactor catalyst and preparation and application thereof, belonging to the technical field of synthesis gas conversion. The catalyst consists of a core of an iron-based Fischer-Tropsch catalyst, a transition layer of a porous oxide or porous carbon material, and a shell layer of a molecular sieve having an aromatization function. The molecular sieve of the shell layer can be further modified by a metal element or a non-metal element, and the outer surface of the molecular sieve is further modified by a silicon-oxygen compound to adjust the acidic site on the outer surface and the aperture of the molecular sieve, thereby inhibiting the formation of heavy aromatic hydrocarbons. According to the disclosure, the shell layer molecular sieve with a transition layer and a shell layer containing or not containing auxiliaries, and with or without surface modification can be prepared by the iron-based Fischer-Tropsch catalyst through multiple steps. The catalyst can be used for direct preparation of aromatic compounds, especially light aromatic compounds, from synthesis gas; the selectivity of light aromatic hydrocarbons in hydrocarbons can be 75% or above, and the content in the liquid phase product is not less than 95%; and the catalyst has good stability and good industrial application prospect.

Disclosed are a composite oxide catalyst for preparing butadiene and a method of preparing the same. More particularly, a composite oxide catalyst, for preparing butadiene, including a metal composite oxide and AlPO.sub.4, and a method of preparing the same are disclosed.

According to the present disclosure, a composite oxide catalyst for preparing butadiene, which includes a specific binder material, prevents generation of ingredients with a high boiling point, has superior catalyst strength, catalytic activity and butadiene yield, and a method of preparing the same are provided.

A method and catalyst for forming higher carbon number products from carbon dioxide is provided. An exemplary catalyst includes red mud including iron and aluminum, and impregnated potassium.