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Coal tar hydrogenation catalyst and preparation method thereof

A hydrogenation catalyst and coal tar technology, which is applied in the direction of catalyst activation/preparation, catalyst carrier, chemical instruments and methods, etc., can solve the problem that the catalyst cannot be directly used as raw material of coal tar, and achieve easy vulcanization, high acidity, and improved utilization rate Effect

Pending Publication Date: 2022-07-15
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The catalyst in this patent cannot be directly used as raw material of coal tar, and coal tar needs to be hydrotreated before the catalyst can be used, and its use has certain limitations.

Method used

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  • Coal tar hydrogenation catalyst and preparation method thereof
  • Coal tar hydrogenation catalyst and preparation method thereof
  • Coal tar hydrogenation catalyst and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0074] (1) Preparation of silicon aluminum material

[0075] The preparation concentration is 80gAl 2 O 3 / L of aluminum sulfate solution and concentration of 50gSiO 2 Silica sol solution with / L and modulus of 2.8 is for use, and a dilute sulfuric acid solution with a concentration of 0.5 mol / L is prepared for use. Formulated with a caustic ratio of 1.15 and a concentration of 180 gAl 2 O 3 / L sodium metaaluminate solution for use.

[0076] Measure 1.0L concentration as 50gSiO 2 / L of silica sol solution was added to the container, and under stirring conditions, slowly add 0.8L of 80gAl 2 O 3 / L of aluminum sulfate solution, this process produces aluminum hydroxide colloid, but the solution still exists in liquid form. Then, a 1 mol / L dilute sulfuric acid solution was added to adjust the pH to 3.5, and the acidification treatment was completed to obtain a mixed solution A.

[0077] Add 1000 mL of deionized water to the 5000 mL reactor as bottom water, start stirring ...

Embodiment 2

[0083] Other conditions are the same as in Example 1, except that the silica sol is changed to water glass solution, the amount of water added at the bottom of the reactor is changed to 800ml, and the pH of the controlled reaction is changed to 8.5 to obtain a dry sample of silicon-alumina material PO-2. The silicon-alumina material P-2 was obtained by calcining at 600 °C for 5 h, and its properties are shown in Table 1.

[0084] Take 500 g of the prepared PO-2 silicon-alumina dry sample, add 5.14 g of corn starch, 9.85 g of acetic acid (85wt%) and 480 g of water, mix well, and then form a spherical shape. 0.7-1.2mm carrier Z2.

[0085] The carrier Z2 was saturated with the solution L1, and dried at 110 °C for 2 h. The catalyst C2 was obtained by calcining at 500 °C for 4 h at a volume ratio of nitrogen and water vapor of 2:1. The specific properties are shown in Table 2.

Embodiment 3

[0087] Other conditions are the same as in Example 1, except that the concentration of the silica sol solution is changed to 70SiO 2 / L, then add 1mol / L dilute sulfuric acid solution, adjust the pH to 4.0, change the mixture A to 25mL / min, the treatment temperature is 250℃, the treatment pressure is 0.4MPa, and the treatment is 4h to obtain a dry sample of silicon-alumina material PO-3, calcined at 600 ℃ for 5h to obtain the silicon-alumina material P-3, whose properties are shown in Table 1.

[0088] Take 500 g of the prepared PO-3 dry sample, add 6.15 g of methyl cellulose, 12.42 g of tartaric acid and 460 g of water, mix well, and then form a spherical shape. 1.2mm carrier Z3.

[0089] The carrier Z3 was saturated with the solution L1 solution, and dried at 110 °C for 2 h. The catalyst C3 was obtained by calcining at 480° C. for 3 h at a volume ratio of nitrogen and water vapor at 1:1. The specific properties are shown in Table 2.

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Abstract

The present invention provides a coal tar hydrogenation catalyst and a preparation method thereof, the catalyst comprises a carrier and an active metal component loaded on the carrier, the carrier is a silicon-aluminum material, the active metal component is at least one of a VIB group metal and / or a VIII group metal, and the active metal component is a silicon-aluminum material. The preparation method comprises the following steps: mixing the silicon-aluminum material, the forming agent and the binder, forming, drying and roasting to obtain the carrier, introducing the active metal component onto the carrier, and further drying and roasting to obtain the coal tar hydrogenation catalyst. The coal tar hydrogenation catalyst provided by the invention has the advantages of high active metal utilization rate, good wear resistance, strong water resistance, high impurity removal rate, high metal capacity, good cracking performance and the like, and is suitable for being applied to a coal tar hydrogenation process.

Description

technical field [0001] The invention belongs to the technical field of petrochemical industry, and relates to a catalytic material and a preparation method thereof, in particular to a hydrogenation catalyst and a preparation method thereof. Background technique [0002] Coal tar is a liquid by-product obtained during the dry distillation and vaporization of coal, which has a pungent odor, black or dark brown, and viscous liquid. Coal tar can be divided into low temperature coal tar, medium temperature coal tar and high temperature coal tar according to the retorting temperature, and the H / C atomic ratio becomes gradually smaller. [0003] Compared with petroleum heavy distillates, coal tar raw materials contain oxygen, a large amount of olefins, polycyclic aromatic hydrocarbons and other unsaturated hydrocarbons, as well as sulfur and nitrogen compounds, which have high acidity, high gum content, and product stability (light stability, storage stability. Therefore, direct c...

Claims

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Application Information

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IPC IPC(8): B01J27/19B01J23/883B01J21/12B01J32/00B01J35/02B01J35/10B01J37/00B01J37/02B01J37/08B01J37/03B01J37/10C10G45/08C10G45/20
CPCB01J27/19B01J23/883B01J23/002B01J21/12B01J37/0018B01J37/0213B01J37/082B01J37/086B01J37/084B01J37/038B01J37/10C10G45/08C10G45/20C10G2300/201C10G2300/205B01J2523/00B01J35/40B01J35/635B01J35/647B01J35/651B01J35/615B01J2523/31B01J2523/41B01J2523/51B01J2523/68B01J2523/847Y02P20/52
Inventor 朱慧红刘铁斌金浩吕振辉杨光刘璐杨涛
Owner CHINA PETROLEUM & CHEM CORP