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Selective hydrogenation method for C2 fraction

A selectivity and fractionation technology, applied in hydrocarbons, chemical instruments and methods, purification/separation of hydrocarbons, etc., can solve problems such as large economic losses and difficulty in uniform loading

Active Publication Date: 2013-12-04
PETROCHINA CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

When the co-impregnation method is used, due to the different interactions between the precursors of the two metal ions and the carrier, as well as the surface tension and solvation, it is difficult to form a uniform loading of the two components, and only a partial alloy structure can be formed.
When this catalyst is used in the selective hydrogenation of carbon distillates, the selectivity is often better at the initial stage of the reaction, and the selectivity continues to decline with the extension of the operating time. Generally, it needs to be regenerated after 3 to 6 months of operation, and the economic loss is relatively large.

Method used

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  • Selective hydrogenation method for C2 fraction
  • Selective hydrogenation method for C2 fraction
  • Selective hydrogenation method for C2 fraction

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0060] Catalyst preparation:

[0061] A. Functionalized polyvinyl chloride (PVC) / Al 2 o 3 preparation of

[0062] Weigh Φ4.5mm, length is 4.5mm, specific surface area is 15.m 2 / g, the pore volume is 0.25ml / g, the bulk density is 1.1g / cm 3 Columnar Al 2 o 3 Carrier 250g.

[0063] Dissolve 4.450g of PVC completely in 400mlTHF (tetrahydrofuran), immerse the above-mentioned carrier into the above-mentioned solution, let the PVC adsorb on Al after standing for 2h 2 o 3 Surface, dry. Get 205gPVC / Al 2 o 3 product.

[0064] Add 59.64g dicyandiamide and 2.0gNa 2 CO 3 ,, add 205g PVC / Al 2 o 3 Reflux for 1 h, cool to room temperature, wash with deionized water until neutral, and dry for later use. Get functionalized PVC / Al 2 o 3 .

[0065] B. (Pd-Ag)-polymer / Al 2 o 3 Precursor preparation

[0066] Weigh 0.165gPd(NO 3 ) 2 , 0.8gAgNO 3 , measure 0.5ml of nitric acid, prepare a mixed solution of 1200ml, weigh the prepared functionalized-PVC / Al 2 o 3 Precursor 255...

Embodiment 2

[0082] Catalyst preparation

[0083] A. Functionalized polystyrene acrylonitrile (SAN) / Al 2 o 3 preparation of

[0084] Weigh Φ2.5mm, the specific surface area is 50m 2 / g, the pore volume is 0.8ml / g, the bulk density is 0.65g / cm 3 spherical Al 2 o 3 Carrier 250g

[0085] Weigh 1.1g of SAN resin, dissolve it in 300ml of DMF (dimethylformamide) solvent, stir at room temperature to completely dissolve the SAN resin, add the above-mentioned weighed carrier in this solution, let it stand for 6 hours after fully stirring, separate Solvent post-drying yields SAN / Al 2 o 3 .

[0086] The above obtained SAN / Al 2 o 3 , added to 500ml deionized water, 28.8g ethylenediamine was added, refluxed for 4h, the product was taken out after cooling, washed until neutral, and dried to obtain functionalized-SAN / Al 2 o 3 .

[0087] B. (Pd-Ag)-SAN / Al 2 o 3 Precursor preparation

[0088] Weigh 0.47gPd(NO 3 ) 2 , 0.4gAgNO 3 , measure 0.5ml of nitric acid, prepare a mixed solution of...

Embodiment 3

[0105] Catalyst preparation

[0106] Weigh Φ4.5mm, length is 4.5mm, specific surface area is 25.m 2 / g, the pore volume is 0.35ml / g, the bulk density is 0.75g / cm 3 Columnar Al 2 o 3 Carrier 250g.

[0107] A, the preparation of functionalized chlorinated polyethylene (CPE)

[0108] Dissolve 8.0g of CPE completely in 400mlTHF, add 240g of dicyandiamide and 2.0g of Na 2 CO 3 ,, add CPE to reflux for 2 hours, cool to room temperature, wash with deionized water until neutral, and obtain functionalized CPE for future use.

[0109] B. (Pd-Ag)-polymer / Al 2 o 3 Precursor preparation

[0110] Weigh 0.22gPd(NO 3 ) 2 , 0.28gAgNO 3 , Measure 0.5ml of nitric acid, add it into the above functionalized CPE solution, and stir for 60min to obtain (Pd—Ag)—CPE.

[0111] Add 250g of the carrier into the mixed solution, stir well and let it stand for 4h, wash the above product with deionized water until neutral to obtain (Pd-Ag)-CPE / Al 2 o 3 Precursor.

[0112] C. Preparation of cat...

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Abstract

The invention relates to a selective hydrogenation method for a C2 fraction, is used for post-hydrogenation, and introduces C2<+> materials from a front dethanizer in an ethylene device to a fixed bed reactor for selective hydrogenation after pressure hydrogen distribution. The selective hydrogenation method is characterized in that: the fixed bed reactor is provided with a Pd-Ag catalyst, Al2O3 or a mixture of Al2O3 and other oxides is used as a carrier, and the catalyst forms an organic polymer metal complex during preparation process; and the reaction conditions are as follows: the inlet temperature of the fixed bed reactor is 40-100 DEG C, the reaction pressure is 1.5-2.5 MPa and the gas space velocity is 2000-10000 h<-1>. The selective hydrogenation method provided by the invention has higher hydrogenation reaction activity and selectivity than traditional hydrogenation methods, and the generation amount of green oil during hydrogenation process greatly decreases, thus maintaining good activity and selectivity of the catalyst.

Description

technical field [0001] The invention relates to a method for selective hydrogenation, in particular to a method for selective hydrogenation of carbon distillates to remove acetylene. Background technique [0002] The production of polymer grade ethylene is the leader of the petrochemical industry, and polymer grade ethylene and propylene are the most basic raw materials for downstream polymerization units. Among them, the selective hydrogenation of acetylene has an extremely important impact on the ethylene processing industry. In addition to ensuring that the acetylene content at the outlet of the hydrogenation reactor reaches the standard, the selectivity of the catalyst is excellent, which can make ethylene generate as little ethane as possible, which is beneficial to improving the entire process. It is of great significance to improve the ethylene yield of the process and improve the economic benefits of the device. [0003] The cracked carbon distillate contains acetyl...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07C11/04C07C7/167B01J23/50
CPCY02P20/52
Inventor 谭都平梁琨王建明车春霞常晓昕高源梁玉龙林宏
Owner PETROCHINA CO LTD
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