Supported Ni-based catalyst for DCPD (dicyclopentadiene) continuous hydrogenation and hydrogenating method

A catalyst, supported technology, applied in metal/metal oxide/metal hydroxide catalysts, chemical instruments and methods, physical/chemical process catalysts, etc., can solve the problem of low operating temperature, high catalyst cost, catalyst hydrogenation activity reduce problems such as reducing reaction temperature and pressure, and achieve the effects of low reaction temperature and pressure, high yield and selectivity, and simple preparation process

Active Publication Date: 2014-06-25
军事科学院系统工程研究院军事新能源技术研究所
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Raney Ni and Pd/C catalysts are used, and the hydrogenation reaction generally needs to be carried out in a slurry bed reactor. The former is gradually deactivated due to the loss of catalyst pulverization during the hydrogenation process. Although the latter has high hydrogenation activity, the cost of the catalyst is relatively high. high
CN101215218B discloses the operating conditions of Raney Ni and Pd/C catalytic DCPD hydrogenation in a tank reactor, but the operation of the batch synthesis process is complicated, the fine powder catalyst is difficult to recycle, and the catalyst cannot be reus

Method used

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  • Supported Ni-based catalyst for DCPD (dicyclopentadiene) continuous hydrogenation and hydrogenating method
  • Supported Ni-based catalyst for DCPD (dicyclopentadiene) continuous hydrogenation and hydrogenating method
  • Supported Ni-based catalyst for DCPD (dicyclopentadiene) continuous hydrogenation and hydrogenating method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0026] Embodiment 1: preparation of catalyst A

[0027] Weigh Ni(NO 3 ) 2 ·6H 2 O crystal 49.82g, Cu(NO 3 ) 2 ·3H 2 O crystal 9.72g, Zn(NO 3 ) 2 ·6H 2 O crystals 8.77g, TiCl 4 Crystal 0.95g, dissolved in 30mL deionized water to prepare impregnation solution, weighed the dried and roasted clover-type γ-A0 with a diameter of 1.6mm 2 o 3 Carrier 60g, add the above impregnating solution drop by drop under stirring to impregnate with equal volume, dry at room temperature, dry at 80°C for 4h, and bake at 500°C for 4h to obtain NiO loading of 16%, CuO loading of 4%, and ZnO loading of 60g. 3% TiO 2 Ni-Cu-Zn-Ti / γ-Al with a loading of 0.5% 2 o 3 Catalyst A.

Embodiment 2

[0028] Embodiment 2: preparation of catalyst B

[0029] Weigh Ni(NO 3 ) 2 ·6H 2 O crystal 49.82g, Cu(NO 3 ) 2 ·3H 2 O crystal 9.72g, Zn(NO 3 )2 ·6H 2 O crystals 8.77g, HfCl 4 Crystal 0.61g, dissolved in 30mL deionized water to prepare impregnation solution, weighed the dried and roasted clover-type γ-Al with a diameter of 1.6mm 2 o 3 Carrier 60g, add the above impregnating solution drop by drop under stirring for equal volume impregnation, dry at room temperature, dry at 80°C for 4h, and bake at 500°C for 4h to obtain NiO loading of 16%, CuO loading of 4%, ZnO loading 3% HfO 2 Ni-Cu-Zn-Hf / γ-Al with a loading of 0.5% 2 o 3 Catalyst B.

Embodiment 3

[0030] Embodiment 3: preparation of catalyst C

[0031] Weigh Zn(NO 3 ) 2 ·6H 2 8.77g of O crystals were dissolved in 50mL of deionized water to prepare an impregnation solution, and the dried and roasted clover-type γ-Al with a diameter of 1.6mm was weighed 2 o 3 Carrier 55g, add the above impregnation solution drop by drop under stirring for equal volume impregnation, dry and roast according to the method of Example 1 to obtain surface ZnO modified γ-Al 2 o 3 carrier; then weigh Ni(NO 3 ) 2 ·6H 2 O crystal 49.82g, Cu(NO 3 ) 2 ·3H 2 O crystals 9.72g, HfCl 4 Crystal 0.61g, dissolved in 30mL deionized water to prepare impregnating liquid, dropwise add above impregnating liquid to ZnO modified γ-Al 2 o 3 Equal volume impregnation was carried out on the carrier, the drying and roasting process was the same as in Example 1, and the NiO loading was 16%, the CuO loading was 4%, the ZnO loading was 3%, and the HfO loading was 16%. 2 Ni-Cu-Zn-Hf / γ-Al with a loading of 0....

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Abstract

The invention relates to a Ni-based catalyst for continuous hydrogenation of a DCPD fixed bed and a hydrogenating method for DCPD continuous hydrogenation to synthesize endo-tetrahydrodicyclopentadiene (endo-THDCPD), overcoming the problems of complex operation, low synthetic efficiency, rapid catalyst deactivation and difficulty in separation of the catalyst and a product for the existing intermittent synthetic reaction. The Ni-based catalyst is prepared from the following components by weight percentage: 5%-40% of NiO, 1-15% of CuO, 0.2%-5% of basic metallic oxide, 0.2%-5% of transition metallic oxide and the balance of a carrier gamma-Al2O3. The catalyst is prepared from a soluble salt solution of reactive metal and auxiliary metal by an impregnation method, and is subjected to drying, calcination and reduction for continuous hydrogenation reaction of a DCPD fixed bed. The Ni-based catalyst is prepared by a co-impregnation method, and also can be prepared by a substep impregnation method, the required reduction temperature is low, the reaction condition is mild, the one-step hydrogenation activity is high, the yield and the selectivity of the endo-THDCPD are high and the activity stability is good.

Description

technical field [0001] The invention relates to a Ni-based catalyst used for DCPD fixed-bed continuous hydrogenation and a hydrogenation method. Background technique [0002] The catalytic hydrogenation product of dicyclopentadiene (abbreviated as DCPD) bridged tetrahydrodicyclopentadiene (abbreviated as endo-THDCPD) is a high-density hydrocarbon fuel hanging tetrahydrodicyclopentadiene (abbreviated as exo- THDCPD, the important chemical intermediate of JP-10 fuel). [0003] The DCPD molecule has two carbon-carbon double bonds, and its hydrogenation reaction equation is as follows: [0004] [0005] Among them, the hydrogenation reaction heat of the 1 and 2 double bonds is -109.7kJ·mol -1 , the hydrogenation reaction heat of the 9, 10-position double bond is -139kJ·mol -1 , it can be seen that the 9 and 10 double bonds are more likely to undergo hydrogenation reactions than the 1 and 2 double bonds. Therefore, the intermediate product of DCPD hydrogenation is mainly 9...

Claims

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Application Information

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IPC IPC(8): B01J23/80B01J23/78B01J23/755C07C13/61C07C5/03
Inventor 安高军鲁长波熊春华赵会吉刘亚文刘晨光王旭东周友杰
Owner 军事科学院系统工程研究院军事新能源技术研究所
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