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PAH Selective Hydrogenation Catalyst

A hydrogenation catalyst, a technology for polycyclic aromatic hydrocarbons, which can be applied in the directions of hydrogenation of aromatic hydrocarbons, molecular sieve catalysts, catalysts for physical/chemical processes, etc., and can solve the problems of low hydrogenation selectivity of polycyclic aromatic hydrocarbons and low yield of monocyclic aromatic hydrocarbons.

Active Publication Date: 2021-10-01
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] The technical problem to be solved by the present invention is that the prior art has the problems of low hydrogenation selectivity of fused-ring aromatics and low yield of single-ring aromatics, and provides a new selective hydrogenation catalyst for fused-ring aromatics, which is used to treat When single-ring aromatics and fused-ring aromatics are used as materials, it has the advantages of high selective hydrogenation rate of fused-ring aromatics and small loss of single-ring aromatics

Method used

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  • PAH Selective Hydrogenation Catalyst
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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] Get 20 grams of alumina ball carrier, impregnate a certain nickel nitrate solution in equal volume, dry at 120°C for 4 hours, and roast at 550°C for 4 hours to obtain modified catalyst A1 with a nickel content of 2% (wt), and impregnate catalyst A1 with equal volume A certain chloroplatinic acid solution was obtained to obtain a core-shell metal layer catalyst B1 with a platinum content of 0.2% (wt).

[0023] Put 5 grams of core-shell metal layer catalyst B1 in the reactor, pass hydrogen to reduce at 450°C for 3 hours, then lower the temperature to 350°C, pass through hydrogen and materials containing toluene and naphthalene to contact with the catalyst to investigate the reaction activity. The reaction conditions are: the total weight space velocity is 10 hours -1 , the reaction temperature is 350°C, the reaction pressure is 3.0MPa, and the molecular ratio of hydrogen to hydrocarbon is 3.0. The reaction raw materials are toluene:naphthalene=90:10 (weight), and the rea...

Embodiment 2

[0025] Get 20 grams of alumina ball carrier, impregnate a certain nickel nitrate solution in equal volume, dry at 120°C for 4 hours, and roast at 550°C for 4 hours to obtain modified catalyst A2 with a nickel content of 5% (wt), impregnate catalyst A2 in equal volume A certain amount of chloroplatinic acid solution was used to obtain the core-shell metal catalyst B2 with a platinum content of 0.2% (wt).

[0026] Put 5 grams of core-shell metal layer catalyst B2 in the reactor, pass hydrogen to reduce at 450°C for 3 hours, then lower the temperature to 350°C, pass through hydrogen and materials containing toluene and naphthalene to contact with the catalyst to investigate the reaction activity. The reaction conditions are: the total weight space velocity is 10 hours -1 , the reaction temperature is 350°C, the reaction pressure is 3.0MPa, and the molecular ratio of hydrogen to hydrocarbon is 3.0. The reaction raw materials are toluene:naphthalene=90:10 (weight), and the reactio...

Embodiment 3

[0028] Get 20 grams of alumina ball carrier, impregnate a certain nickel nitrate solution in equal volume, dry at 120°C for 4 hours, and roast at 550°C for 4 hours to obtain modified catalyst A3 with a nickel content of 2% (wt), impregnate catalyst A3 in equal volume A certain chloroplatinic acid solution was obtained to obtain a core-shell metal layer catalyst B3 with a platinum content of 0.5% (wt).

[0029] Put 5 grams of core-shell metal layer catalyst B3 in the reactor, pass hydrogen to reduce at 450°C for 3 hours, then lower the temperature to 350°C, pass through hydrogen and materials containing toluene and naphthalene to contact the catalyst to investigate the reaction activity. The reaction conditions are: the total weight space velocity is 10 hours -1 , the reaction temperature is 350°C, the reaction pressure is 3.0MPa, and the molecular ratio of hydrogen to hydrocarbon is 3.0. The reaction raw materials are toluene:naphthalene=90:10 (weight), and the reaction perfo...

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Abstract

The invention relates to a catalyst for selective hydrogenation of polycyclic aromatic hydrocarbons, which mainly solves the problems in the prior art that the hydrogenation selectivity of polycyclic aromatic hydrocarbons is not high and the loss rate of single-ring aromatic hydrocarbons is high. The present invention adopts a polycyclic aromatic hydrocarbon selective hydrogenation catalyst, comprising: containing non-acidic or weakly acidic porous carrier, and at least two metal elements or compounds selected from group VIII supported thereon, the metal elements or compounds are in The technical scheme of core-shell distribution on the surface of the carrier can significantly improve the hydrogenation selectivity of polycyclic aromatic hydrocarbons and reduce the loss of single-ring aromatic hydrocarbons.

Description

technical field [0001] The invention relates to a polycyclic aromatic hydrocarbon selective hydrogenation catalyst and a preparation method thereof. Background technique [0002] Polycyclic aromatic hydrocarbons refer to aromatic hydrocarbon components with bicyclic and polycyclic structures, which exist in large quantities in catalytic cracking, ethylene tar and PX production processes. For example, the annual output of catalytic cracking light cycle oil has exceeded 10 million, and most of them are used as diesel blending components. In recent years, with the increasing demand for PX in my country, the supply of PX has been in short supply. One of the key factors to solve the current problems is to realize the large-scale and diversified raw materials of the aromatics complex. Therefore, it is of great significance to make full use of the condensed-ring aromatics produced by the aromatics complex and to study the use of the by-product fused-ring aromatics in the refinery ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): B01J23/89B01J29/76C10G45/46C10G45/50C10G45/54
CPCC10G45/46C10G45/50C10G45/54B01J23/002B01J23/8906B01J23/8913B01J23/892B01J29/7615B01J2523/00B01J2229/18B01J35/397B01J2523/31B01J2523/842B01J2523/847
Inventor 李经球李华英孔德金
Owner CHINA PETROLEUM & CHEM CORP