A perovskite-type oxide catalyst for water-splitting reactions is provided. The catalyst, Ca.sub.2-ySr.sub.yFe.sub.1-xCo.sub.1-xMn.sub.2xO.sub.6-δ where y=0.10-1.90 and x=0.05-0.95, has catalytic activity for both hydrogen- and oxygen-evolution reactions. An exemplary catalyst is CaSrFe.sub.0.75Co.sub.0.75Mn.sub.0.5O.sub.6-δ.

The present invention relates to a method for preparing a polyether amine catalyst, and polyether amine. A polyether amine catalyst is a supported metal catalyst; γ-Al.sub.2O.sub.3 is used as a carrier; basic cupric carbonate, basic nickel carbonate and basic cobalt carbonate are used as precursors of supported metals; and the polyether amine catalyst is prepared by performing twice adsorption roasting and once reduction by means of an equivalent-volumetric impregnation method. Easier decomposition is achieved by using basic carbonate, and only water and carbon dioxide are generated, such that processes and costs for treating waste gases can be saved. By using the polyether amine catalyst to prepare polyether amine, a conversion rate and primary amine selectivity can be improved, and the color of products can be reduced. Therefore, the obtained polyether amine can have higher activity and wider application.

There are provided an ammoxidation catalyst for propylene, a manufacturing method of the same, and an ammoxidation method of propylene using the same. Specifically, according to one embodiment of the invention, a catalyst is realized with a structure in which metal oxide is supported on a silica carrier, and thus, using mesopores useful for adsorption and desorption of gas, a high reaction surface area can be provided, and ultimately, ammoxidation of propylene can be increased.

There are provided an ammoxidation catalyst for propylene, a manufacturing method of the same, and an ammoxidation method of propylene using the same. Specifically, according to one embodiment of the invention, a catalyst is realized with a structure in which metal oxide is supported on a silica carrier, and thus, using mesopores useful for adsorption and desorption of gas, a high reaction surface area can be provided, and ultimately, ammoxidation of propylene can be increased.

Embodiments of the present disclosure include a metal-organic framework (MOF) composition comprising one or more metal ions, a plurality of organic ligands, and a solvent, wherein the one or more metal ions associate with the plurality of organic ligands sufficient to form a MOF with kag topology. Embodiments of the present disclosure further include a method of making a MOF composition comprising contacting one or more metal ions with a plurality of organic ligands in the presence of a solvent, sufficient to form a MOF with kag topology, wherein the solvent comprises water only. Embodiments of the present disclosure also describe a method of capturing chemical species from a fluid composition comprising contacting a MOF composition with kag topology and pore size of about 3.4 Å to 4.8 Å with a fluid composition comprising two or more chemical species and capturing one or more captured chemical species from the fluid composition.

The present disclosures and inventions relate to a catalyst composition for the selective conversion of a hydrogen/carbon monoxide mixture (syngas) to C2+ hydrocarbons. The composition includes a catalyst having the formula CoMn.sub.xSi.sub.yO.sub.z, wherein the molar ratio of x is from about 0.8 to about 1.2; wherein the molar ratio of y is from about 0.1 to about 1.0; and wherein the molar ratio of z is a number determined by the valence requirements of Co, Mn, and Si wherein the catalyst has a Scherrer crystallite size of less than about 40 nm, wherein the Si is silica.

The present disclosures and inventions relate to a catalyst composition for the selective conversion of a hydrogen/carbon monoxide mixture (syngas) to C2+ hydrocarbons. The composition includes a catalyst having the formula CoMn.sub.xSi.sub.yO.sub.z, wherein the molar ratio of x is from about 0.8 to about 1.2; wherein the molar ratio of y is from about 0.1 to about 1.0; and wherein the molar ratio of z is a number determined by the valence requirements of Co, Mn, and Si wherein the catalyst has a Scherrer crystallite size of less than about 40 nm, wherein the Si is silica.

A method of loading granules into reaction tubes of a vertical multitube reactor installed in a vertical direction by dropping the granules from above each of the reaction tubes in a state that a linear member is inserted and suspended in the reaction tube. The reaction tube has an effective length of 1000 mm or more. The linear member includes a small-diameter portion positioned on an upper side and a large-diameter portion continuously extending from the small-diameter portion. The small-diameter portion has an outer diameter (Ra) of 5.0 mm or less, and the large-diameter portion has an outer diameter (Rb) of 5.0 to 15.0 mm larger than the outer diameter (Ra). A length of the small-diameter portion from an upper end of the reaction tube is 10.0 mm or more. A distance between an upper surface of a granule loaded layer formed inside the reaction tube and a lower end of the linear member inserted in the reaction tube is 100 mm or more.

A method of loading granules into reaction tubes of a vertical multitube reactor installed in a vertical direction by dropping the granules from above each of the reaction tubes in a state that a linear member is inserted and suspended in the reaction tube. The reaction tube has an effective length of 1000 mm or more. The linear member includes a small-diameter portion positioned on an upper side and a large-diameter portion continuously extending from the small-diameter portion. The small-diameter portion has an outer diameter (Ra) of 5.0 mm or less, and the large-diameter portion has an outer diameter (Rb) of 5.0 to 15.0 mm larger than the outer diameter (Ra). A length of the small-diameter portion from an upper end of the reaction tube is 10.0 mm or more. A distance between an upper surface of a granule loaded layer formed inside the reaction tube and a lower end of the linear member inserted in the reaction tube is 100 mm or more.

The invention provides a process for preparing a cobalt-containing catalyst precursor. The process includes calcining a loaded catalyst support comprising a silica (SiO.sub.2) catalyst support supporting cobalt nitrate to convert the cobalt nitrate into cobalt oxide. The calcination includes heating the loaded catalyst support at a high heating rate, which does not fall below 10° C./minute, during at least a temperature range A. The temperature range A is from the lowest temperature at which calcination of the loaded catalyst support begins to 165° C. Gas flow is effected over the loaded catalyst support during at least the temperature range A. The catalyst precursor is reduced to obtain a Fischer-Tropsch catalyst.