Disclosed are a chemochromic nanoparticle, a method for manufacturing the chemochromic nanoparticle, and a hydrogen sensor comprising the chemochromic nanoparticle. In particular, the chemochromic nanoparticle has a core-shell structure such that the chemochromic nanoparticle and comprises a core comprising a hydrated or non-hydrated transition metal oxide; and a shell comprising a transition metal catalyst.

Provided are a carbon-based noble metal-transition metal composite catalyst enabling high selective conversion of a carboxylic acid functional group into an alcohol functional group by pre-treating a carbon carrier including a predetermined ratio or more of mesopores, and a production method therefor.

Provided are a noble metal-transition metal complex catalyst supported on a carbon-coated silica-alumina support and a preparation method therefor, the catalyst being capable of obtaining a fast reaction rate and catalyst stability, as compared to a conventional catalyst, when cyclohexane dimethanol (CHDM) production is carried out by a cyclohexane dicarboxylic acid (CHDA) hydrogenation reaction in an aqueous solution by using a carbon-coated supported catalyst.

The present invention provides a production method for indene, comprising a dehydrogenation step of obtaining a reaction product containing indene by contacting a raw material composition containing indene with a dehydrogenation catalyst, wherein the dehydrogenation catalyst comprises a support containing aluminum, and a group 14 metal element and platinum supported on the support, a content of the platinum in the dehydrogenation catalyst is 0.6 to 2.5% by mass based on a whole amount of the dehydrogenation catalyst, and an atomic ratio of the group 14 metal element to the platinum in the dehydrogenation catalyst is 4.0 to 20.0.

The present invention provides a production method for indene, comprising a dehydrogenation step of obtaining a reaction product containing indene by contacting a raw material composition containing indene with a dehydrogenation catalyst, wherein the dehydrogenation catalyst comprises a support containing aluminum, and a group 14 metal element and platinum supported on the support, a content of the platinum in the dehydrogenation catalyst is 0.6 to 2.5% by mass based on a whole amount of the dehydrogenation catalyst, and an atomic ratio of the group 14 metal element to the platinum in the dehydrogenation catalyst is 4.0 to 20.0.

The present invention relates to a dehydrogenation catalyst in which a platinum-group metal, an assistant metal, and an alkali metal or alkaline earth metal component are supported on a carrier, wherein the molar ratio of platinum to the assistant metal is 0.5 to 1.49, and the catalyst has an acidity amount of 20 to 150 mol KOH/g catalyst when it is titrated with KOH. The dehydrogenation catalyst according to the present invention may prevent coke formation from increasing rapidly when the hydrogen/hydrocarbon ratio in a dehydrogenation reaction is reduced, thereby increasing the productivity of the process. Accordingly, it makes it possible to operate the process under a condition in which the hydrogen/hydrocarbon ratio in a dehydrogenation reaction is reduced, thereby improving the economy of the process.

The present invention relates to a dehydrogenation catalyst in which a platinum-group metal, an assistant metal, and an alkali metal or alkaline earth metal component are supported on a carrier, wherein the molar ratio of platinum to the assistant metal is 0.5 to 1.49, and the catalyst has an acidity amount of 20 to 150 mol KOH/g catalyst when it is titrated with KOH. The dehydrogenation catalyst according to the present invention may prevent coke formation from increasing rapidly when the hydrogen/hydrocarbon ratio in a dehydrogenation reaction is reduced, thereby increasing the productivity of the process. Accordingly, it makes it possible to operate the process under a condition in which the hydrogen/hydrocarbon ratio in a dehydrogenation reaction is reduced, thereby improving the economy of the process.

The present disclosure relates to dehydrogenation catalysts based on one or more certain group 13 and group 14 elements that further include additional metal components, to methods for making such catalysts, and to methods for dehydrogenating hydrocarbons using such catalysts. One aspect of the disclosure provides a calcined dehydrogenation catalyst that includes a primary species P1 selected from the group consisting of Ga, In, Tl, Ge, Sn and Pb and combinations thereof; a primary species P2 selected from the lanthanides; a promoter M1 selected from the group consisting of Ni, Pd and Pt; a promoter M2 selected from the group consisting of Li, Na, K, Rb, Cs, Be, Mg, Ca, Sr and Ba, on a silica-alumina support.

The present disclosure relates to dehydrogenation catalysts based on one or more certain group 13 and group 14 elements that further include additional metal components, to methods for making such catalysts, and to methods for dehydrogenating hydrocarbons using such catalysts. One aspect of the disclosure provides a calcined dehydrogenation catalyst that includes a primary species P1 selected from the group consisting of Ga, In, Tl, Ge, Sn and Pb and combinations thereof; a primary species P2 selected from the lanthanides; a promoter M1 selected from the group consisting of Ni, Pd and Pt; a promoter M2 selected from the group consisting of Li, Na, K, Rb, Cs, Be, Mg, Ca, Sr and Ba, on a silica-alumina support.

A catalytic composite comprises a first component selected from Group VIII noble metal components and mixtures thereof, a second component selected from one or more of alkali and alkaline earth metal components, and a third component selected from one or more of tin, germanium, lead, indium, gallium, and thallium, all supported on an alumina support comprising delta alumina having an X-ray diffraction pattern comprising at least three 2 diffraction angle peaks between 32.0 and 70.0. The at least three 2 diffraction angle peaks comprise a first 2 diffraction angle peak of 32.70.4, a second 2 diffraction angle peak of 50.80.4, and a third 2 diffraction angle peak of 66.70.8, wherein the second 2 diffraction angle peak has an intensity of less than about 0.06 times the intensity of the third 2 diffraction angle peak.