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Coke oven gas hydrogenation and desulfurization catalyst and method for preparing same

A technology for hydrodesulfurization and coke oven gas, applied in chemical instruments and methods, metal/metal oxide/metal hydroxide catalysts, heterogeneous catalyst chemical elements, etc., can solve problems such as environmental pollution, and achieve environmental friendliness , the method is simple, the effect of convenient operation

Active Publication Date: 2018-08-17
XIAN SUNWARD AEROSPACE MATERIAL CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0010] The vulcanization process generally uses carbon disulfide or dimethyl disulfide as the vulcanizing agent. In order to ensure the complete vulcanization of the catalyst, an excessive amount of vulcanizing agent needs to be used. The sulfur-containing tail gas produced by vulcanization is generally incinerated, and a large amount of SO is emitted. 2 gas, causing serious environmental pollution

Method used

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  • Coke oven gas hydrogenation and desulfurization catalyst and method for preparing same
  • Coke oven gas hydrogenation and desulfurization catalyst and method for preparing same
  • Coke oven gas hydrogenation and desulfurization catalyst and method for preparing same

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Embodiment 1

[0028] The coke oven gas hydrodesulfurization catalyst of the present embodiment is made of the raw material of following mass percent: SiO 2 0.1%, B 2 o 3 0.1%, MoO 3 8.0%, Al 2 o 3 91.8%; the preparation method of this coke oven gas hydrodesulfurization catalyst is: take by weighing ammonium dimolybdate 18.9g and be dissolved in 110g water, add 0.5g tetramethoxysilane after dissolving, add sulfuric acid 0.30g, boric acid 0.04g, add 184g of alumina carrier, dry at 120°C for 12h after impregnation, and then calcinate at 500°C for 2h to obtain the finished catalyst.

Embodiment 2

[0030] The coke oven gas hydrodesulfurization catalyst of the present embodiment is made of the raw material of following mass percent: SiO 2 0.1%, P 2 o 5 0.1%, MoO 3 8.0%, Al2 o 3 91.8%; the preparation method of this coke oven gas hydrodesulfurization catalyst is: take by weighing ammonium dimolybdate 18.9g and be dissolved in 110g water, add 0.25g tetramethoxysilane and 0.2g trimethoxysilane after dissolving, under stirring condition Add 0.30g of sulfuric acid and 0.03g of phosphoric acid, add 184g of alumina carrier, dry at 120°C for 12h after impregnation, and then roast at 500°C for 2h to obtain the finished catalyst.

Embodiment 3

[0032] The coke oven gas hydrodesulfurization catalyst of the present embodiment is made of the raw material of following mass percent: SiO 2 1.0%, B 2 o 3 0.2%, MoO 3 9.0%, Al 2 o 3 89.8%.

[0033] The preparation method of this coke oven gas hydrodesulfurization catalyst is: take by weighing ammonium tetramolybdate 19.6g and add in 90g water, adjust solution pH with ammonia water to be 9 and make ammonium tetramolybdate dissolve, then add 6.9g tetraethoxysilane, in Add 8.0 g of nitric acid, 0.7 g of boric acid, and 180 g of alumina carrier under stirring conditions. After impregnation, dry at 120°C for 12 hours, and then roast at 300°C for 10 hours to obtain a finished catalyst.

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PUM

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Abstract

The invention discloses a coke oven gas hydrogenation and desulfurization catalyst. Al2O3 is used as a carrier for the coke oven gas hydrogenation and desulfurization catalyst, Mo is used as an activecomponent for the coke oven gas hydrogenation and desulfurization catalyst, Si is used as a first accelerator for the coke oven gas hydrogenation and desulfurization catalyst, B and / or P are used assecond accelerators for the coke oven gas hydrogenation and desulfurization catalyst, the Mo active component exists in the form of MoO3, the first accelerator Si exists in the form of SiO2, the second accelerators exist in the form of second accelerator oxide, the second accelerator P exists in the form of P2O5, and the second accelerator B exists in the form of B2O3. The invention further provides a method for preparing the coke oven gas hydrogenation and desulfurization catalyst. The method includes preparing silicon-molybdenum co-impregnation liquid; carrying out drying and calcining to obtain the coke oven gas hydrogenation and desulfurization catalyst. The coke oven gas hydrogenation and desulfurization catalyst can be directly used without being calcined. The coke oven gas hydrogenation and desulfurization catalyst and the method have the advantages that the coke oven gas hydrogenation and desulfurization catalyst is a silicon-molybdenum catalyst and is high in initial activityand good in heat resistance, the method is simple and is convenient to operate, and industrial production can be facilitated; the accelerators do not need to be vulcanized before being used, and accordingly the usage amounts of vulcanizing agents can be reduced.

Description

technical field [0001] The invention belongs to the technical field of desulfurization catalysts, and in particular relates to a coke oven gas hydrogenation desulfurization catalyst and a preparation method thereof. Background technique [0002] Coke oven gas is a by-product of coking in coking plants, and its main components are methane, hydrogen, carbon monoxide and carbon dioxide. The recovery and utilization of coke oven gas plays an important role in the clean utilization of coal resources in our country. Generally, coke oven gas can be used to produce synthetic ammonia, methanol, H 2 , LNG and other products. In these technological processes, the coke oven gas must be purified first, and the desulfurization process is particularly important. [0003] Usually in the desulfurization process, the coke oven gas still contains 10mg / Nm after wet desulfurization to remove most of the sulfur-containing substances 3 ~200mg / Nm 3 H 2 S and 10mg / Nm 3 ~200mg / Nm 3 of organic...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/28B01J27/18C10K1/00C10K1/34
CPCB01J23/002B01J23/28B01J27/18B01J2523/00C10K1/004C10K1/34B01J2523/305B01J2523/31B01J2523/41B01J2523/68B01J2523/51B01J27/19B01J21/02B01J21/12C10G45/04
Inventor 许龙龙彭东侯亚楠李荣余阳冯毅敏
Owner XIAN SUNWARD AEROSPACE MATERIAL CO LTD
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