Abstract: Disclosed are a hydrogenation catalyst, a preparation method for same, and applications thereof. Also disclosed is a hydrogenation reaction method employing the hydrogenation catalyst. The hydrogenation catalyst of the present invention comprises a binding agent and an active component. The active component comprises nickel and a group VIB metal element. The binding agent comprises zirconium oxide and aluminum oxide. The catalyst of the present invention has nickel serving as the main active ingredient and is inexpensive. Moreover, the catalyst of the present invention exhibits an increased catalytic activity in a hydrogenation reaction of phenolic compounds and specifically provides an increased low-temperature reaction activity. The catalyst of the present invention is applicable in a continuous production process, thus implementing the continuous production of a hydrogenated bisphenol A product and providing the product with high and stable quality.

Abstract: Disclosed are hydrogenation catalysts and a method for a benzoic acid hydrogenation reaction. The hydrogenation catalysts comprise a carrier, and an active component, an auxiliary component, and an alkali metal element that are loaded on the carrier. The active component is ruthenium. The auxiliary component is one or two or more of nickel, iron and cobalt. The method for the hydrogenation reaction comprises a first hydrogenation step and a second hydrogenation step. A first hydrogenation catalyst and a second hydrogenation catalyst are the hydrogenation catalyst. The hydrogenation catalysts according to the present invention have high catalytic activity at a low temperature, and can react under relatively mild reaction conditions. The hydrogenation reaction method according to the present invention can implement the continuous and stable operation of a device, and meets industrial-scale operation requirements.

Abstract: Provided is a reformate hydrotreatment method, the method comprising: under liquid phase hydrotreatment conditions, bringing the reformate and a catalyst having a catalytic hydrogenation effect into contact in a hydrogenation reactor, the hydrogen used in the hydrotreating process at least partially coming from the hydrogen dissolved in the reformate. According to the method of the present invention, the reformate separated from a reformate products separating tank can directly undergo liquid phase hydrotreatment; therefore not only can the hydrogen dissolved in the reformate be fully utilized, but the olefins in the reformate can also be removed, while eliminate the requirements for recycle hydrogen and a recycle device thereof. The reformate obtained by the method of the present invention reduces the bromine index to below 50 mgBr2/100 g, and has an arene loss of less than 0.5 wt %.

Abstract: Provided is a hydrocarbon oil hydrotreating method, comprising the following steps: (1) injecting hydrogen into the hydrocarbon oil via an opening having a nanoscale average diameter, so as to obtain hydrocarbon oil containing hydrogen; and (2) under a liquid phase hydrotreating condition, feeding into a reactor the hydrocarbon oil containing hydrogen to contact a catalyst having a hydrogenation catalysis effect. The method of the present invention can quickly and efficiently disperse and dissolve the hydrogen into the hydrocarbon oil even without the aid of a diluent or circulating oil, so as to obtain stable hydrogen-containing hydrocarbon oil with a high hydrogen content, and obtain an hydrotreating effect equivalent to or even better than the existing hydrotreating methods.

Abstract: Provided is a hydrocarbon oil hydrotreating method, comprising the following steps: (1) injecting hydrogen into the hydrocarbon oil via an opening having a nanoscale average diameter, so as to obtain hydrocarbon oil containing hydrogen; and (2) under a liquid phase hydrotreating condition, feeding into a reactor the hydrocarbon oil containing hydrogen to contact a catalyst having a hydrogenation catalysis effect. The method of the present invention can quickly and efficiently disperse and dissolve the hydrogen into the hydrocarbon oil even without the aid of a diluent or circulating oil, so as to obtain stable hydrogen-containing hydrocarbon oil with a high hydrogen content, and obtain an hydrotreating effect equivalent to or even better than the existing hydrotreating methods.

Abstract: Disclosed herein are a catalyst, a preparation process thereof, and a process of epoxidizing olefin using the catalyst. The catalyst contains a binder and a titanium silicate as specified. The catalyst disclosed herein has high strength, and shows high catalytic activity in the epoxidation of olefins.

Abstract: Provided is a reformate hydrotreatment method, the method comprising: under liquid phase hydrotreatment conditions, bringing the reformate and a catalyst having a catalytic hydrogenation effect into contact in a hydrogenation reactor, the hydrogen used in the hydrotreating process at least partially coming from the hydrogen dissolved in the reformate. According to the method of the present invention, the reformate separated from a reformate products separating tank can directly undergo liquid phase hydrotreatment; therefore not only can the hydrogen dissolved in the reformate be fully utilized, but the olefins in the reformate can also be removed, while eliminate the requirements for recycle hydrogen and a recycle device thereof. The reformate obtained by the method of the present invention reduces the bromine index to below 50 mgBr2/100 g, and has an arene loss of less than 0.5 wt %.

Abstract: The present invention provides a catalyst and the preparation process thereof and a process of epoxidising olefin using the catalyst. The catalyst contains a binder and a titanium silicate, the binder being an amorphous silica, the titanium silicate having a MFI structure, and the crystal grain of the titanium silicate having a hollow structure, with a radial length of 5-300 nm for the cavity portion of the hollow structure, wherein the adsorption capacity of benzene measured for the titanium silicate under the conditions of 25 degrees C., P/P0=0.