C07C2523/89

Process for preparing perhydrofluorene or alkyl-substituted perhydrofluorene

The present invention discloses a process for preparing perhydrofluorene or alkyl-substituted perhydrofluorene, comprising the steps of: (1) reacting a phenolic compound or an aromatic hydrocarbon compound or an aromatic ketone compound or an aromatic ether compound with a benzyl compound to carry out an alkylation reaction in the presence of a first catalyst, thereby to produce substituted or unsubstituted diphenyl methane, wherein the first catalyst is an acidic catalyst; and (2) reacting the substituted or unsubstituted diphenyl methane with hydrogen gas to carry out an hydrogenation reaction or a hydrodeoxygenation reaction, thereby to produce perhydrofluorene or alkyl-substituted perhydrofluorene, wherein the second catalyst is a physical mixture of a metal catalyst and an acidic catalyst or a metal catalyst loaded on an acidic catalyst.

Processes for Regenerating Catalysts and for Upgrading Alkanes and/or Alkyl Aromatic Hydrocarbons

Processes for regenerating an at least partially deactivated catalyst that can include a Group (10) element, an inorganic support, and a contaminant. The Group (10) element can have a concentration of from 0.001 wt % to 6 wt %, based on the weight of the inorganic support. The process can include (I) heating the deactivated catalyst using a heating gas mixture that includes H.sub.2O at a concentration >5 mol %, based on the total moles in the mixture to produce a precursor catalyst. The process can also include (II) providing an oxidative gas that includes ?5 mol % of H.sub.2O, based on the total moles in the oxidative gas, and (III) contacting the precursor catalyst at an oxidizing temperature with the oxidative gas for a duration of at least 30 seconds to produce an oxidized precursor catalyst. The process can also include (IV) obtaining a regenerated catalyst from the oxidized precursor catalyst.

ALKANE ACTIVATION WITH SINGLE AND BI-METALLIC CATALYSTS
20190062235 · 2019-02-28 ·

Methods, compositions, and articles of manufacture for alkane activation with single- or bi-metallic catalysts on crystalline mixed oxide supports.

Binder-free high strength, low steam-to-oil ratio ethylbenzene dehydrogenation catalyst
10195591 · 2019-02-05 · ·

The invention discloses a binder-free high strength and low steam-to-oil ratio ethylbenzene dehydrogenation catalyst, which is characterized by comprising the following components in percentage by weight: (a) 60-85% Fe.sub.2O.sub.3; (b) 3-25% K.sub.2O; (c) 0.1-5% MoO.sub.3; (d) 3-20% CeO.sub.2; (e) 0.1-5% CaO; (f) 0.1-5% Na.sub.2O; (g) 0.1-5% MnO.sub.2, wherein the weight ratio of sodium oxide to manganese dioxide is 0.1-10; (h) 0.1-100 ppm of at least one element or oxide of Pb, Pt, Pd, Ag, Au, Sn; and no binder is added during the preparation of the catalyst. The low steam-to-oil ratio ethylbenzene dehydrogenation catalyst provided by the present invention contains no binder and maintains high strength, and has high activity and stability at low steam-to-oil ratio.

A Process for Preparing Perhydrofluorene or Alkyl-Substituted Perhydrofluorene
20190031576 · 2019-01-31 ·

The present invention discloses a process for preparing perhydrofluorene or alkyl-substituted perhydrofluorene, comprising the steps of: (1) reacting a phenolic compound or an aromatic hydrocarbon compound or an aromatic ketone compound or an aromatic ether compound with a benzyl compound to carry out an alkylation reaction in the presence of a first catalyst, thereby to produce substituted or unsubstituted diphenyl methane, wherein the first catalyst is an acidic catalyst; and (2) reacting the substituted or unsubstituted diphenyl methane with hydrogen gas to carry out an hydrogenation reaction or a hydrodeoxygenation reaction, thereby to produce perhydrofluorene or alkyl-substituted perhydrofluorene, wherein the second catalyst is a physical mixture of a metal catalyst and an acidic catalyst or a metal catalyst loaded on an acidic catalyst.

DEHYDROGENATION CATALYST FOR ALKYLAROMATIC COMPOUND, PROCESS FOR PRODUCING SAME, AND DEHYDROGENATION METHOD USING SAME

A catalyst which is highly active in dehydrogenation reaction of an alkylaromatic hydrocarbon not only in high-temperature regions (e.g. 600 to 650 C.) as found in the inlet of a catalyst bed in an apparatus for the production of SM but also in low-temperature regions (e.g. under 600 C.) as found in the outlet of a catalyst bed in an apparatus for the production of SM, where the temperature decreases as a result of endothermic reaction; and a process for producing the catalyst; and a dehydrogenation process using the catalyst.

The catalyst contains iron (Fe), potassium (K), and cerium (Ce), and at least one rare earth element other than cerium.

Catalyst Compositions and Processes for Making and Using Same

Catalyst compositions and processes for making and using same. The catalyst composition can include catalyst particles. The catalyst particles can include 0.001 wt % to 6 wt % of Pt and up to 10 wt % of a promoter that can include Sn, Cu, Au, Ag, Ga, or a combination thereof, or a mixture thereof disposed on a support. The support can include at least 0.5 wt % of a Group 2 element. All weight percent values are based on the weight of the support. The catalyst particles can have a median particle size in a range from 10 ?m to 500 pm. The catalyst particles can have an apparent loose bulk density in a range from 0.3 g/cm.sup.3 to 2 g/cm.sup.3, as measured according to ASTM D7481-18 modified with a 10, 25, or 50 mL graduated cylinder instead of a 100 or 250 mL graduated cylinder.

Continuous process for preparing ethylene glycol from a carbohydrate source

Ethylene glycol is prepared from a carbohydrate source by reaction of the carbohydrate source with hydrogen in a continuous process, wherein hydrogen, the carbohydrate source and a liquid diluent are continuously fed into a continuous stirred tank reactor wherein a catalyst system is present, which catalyst system comprises a tungsten compound and at least one hydrogenolysis metal selected from the groups 8, 9 or 10 of the Periodic Table of the Elements, to achieve the reaction between the carbohydrate source and hydrogen to ethylene glycol; wherein continuously a product mixture comprising ethylene glycol and diluent is removed from the continuous stirred tank reactor; and wherein continuously or periodically further at least a tungsten compound is added to the continuous stirred tank reactor (CSTR).

Binder-free high strength, low steam-to-oil ratio ethylbenzene dehydrogenation catalyst
20180318807 · 2018-11-08 · ·

The invention discloses a binder-free high strength and low steam-to-oil ratio ethylbenzene dehydrogenation catalyst, which is characterized by comprising the following components in percentage by weight: (a) 60-85% Fe.sub.2O.sub.3; (b) 3-25% K.sub.2O; (c) 0.1-5% MoO.sub.3; (d) 3-20% CeO.sub.2; (e) 0.1-5% CaO; (f) 0.1-5% Na.sub.2O; (g) 0.1-5% MnO.sub.2, wherein the weight ratio of sodium oxide to manganese dioxide is 0.1-10; (h) 0.1-100 ppm of at least one element or oxide of Pb, Pt, Pd, Ag, Au, Sn; and no binder is added during the preparation of the catalyst. The low steam-to-oil ratio ethylbenzene dehydrogenation catalyst provided by the present invention contains no binder and maintains high strength, and has high activity and stability at low steam-to-oil ratio.

Palladium-Based Supported Hydrogenation Catalyst, And Preparation Method And Application Thereof

The present invention relates to a palladium-based supported hydrogenation catalyst and a preparation method and application thereof. The catalyst is prepared by the following method: impregnating an Al.sub.2O.sub.3-containing carrier with an organic solution containing a bipyridine derivative having hydroxy group, optionally drying followed by impregnating with a mixed solution containing the main active component palladium ions and the auxiliary active component M.sup.n+ ions, where M is one selected from Ag, Au, Ni, Pb and Cu; and then optionally drying, and calcining to obtain the catalyst. The preparation method provided by the present invention allows Pd atoms and M atoms to be highly uniformly dispersed on the carrier, which overcomes the adverse impact of the surface tension of the impregnation solution and the solvation effect on the dispersibility of active components. The palladium-based supported hydrogenation catalyst provided by the present invention has excellent hydrogenation activity, ethylene selectivity and anti-coking performance, and can be used in a selective hydrogenation process of C2 fraction.