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Hydrotreating catalyst and preparation method thereof

A technology for hydrotreating and catalyst, which is applied in catalyst activation/preparation, physical/chemical process catalyst, catalyst carrier, etc., can solve the problems of low impurity removal rate, low utilization rate of pore space, and inability to penetrate large pores. To achieve the effect of improving the ability

Active Publication Date: 2011-05-11
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The carrier alumina used is formed by kneading alumina scraps and aluminum hydroxide dry rubber powder. Although the alumina carrier obtained by this method has some large pores, the large pores have two disadvantages. One is that the large pores cannot Second, the active metal in the macropore can only be on the pore wall
The large pores of the residual oil catalyst, especially the too many micron-sized pores are conducive to the diffusion of reactants, but from another perspective, too large pores and low space utilization are not conducive to the reaction, and the removal rate of impurities is low

Method used

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  • Hydrotreating catalyst and preparation method thereof
  • Hydrotreating catalyst and preparation method thereof
  • Hydrotreating catalyst and preparation method thereof

Examples

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Effect test

Embodiment 1

[0039] Under stirring conditions, 375g of aluminum nitrate nonahydrate and 90g of urea were mixed and heated to 100°C, and added to a mixture of 32g of polyisobutylene maleate triethanolamine maleate and 88g of 150HVI neutral oil at the same temperature to form supersolubilizing micelles , and then reacted at 100°C for 3 hours to obtain nano-aluminum hydroxide gel. Wash three times with 200ml of distilled water, and dry at 120°C for 10 hours. Mix 70g of nano-aluminum hydroxide gel dry powder with 30g of binder pseudo-boehmite, 2.6g of dilute nitric acid (mass concentration 17%) and 18g of water, and then shape it in an extruder. The molded product was dried at 100°C for 10 hours, calcined at 240°C for 3 hours, and then calcined at 850°C for 4 hours with a heating rate of 5°C / min to obtain the alumina carrier A1 of the present invention.

[0040] 162g contains MoO 3 Add 82% (weight) ammonium molybdate and 120g of CoO 25% (weight) cobalt nitrate into 35% (weight) 500ml ammonia...

Embodiment 2

[0043] Mix 90g minus three-line dewaxed oil and 70g SP-80, heat to dissolve at 80°C, and mix well; heat 620g of aluminum nitrate nonahydrate to 80°C to melt, slowly add to the above mixture, and mix for 20 minutes to form a uniform supersolubilized colloid. 220 g of saturated ammonia water at 20° C. was added dropwise and aged for 3 hours to obtain a nano-aluminum hydroxide gel. Wash three times with 200ml of distilled water, and dry at 120°C for 10 hours. Mix 70g of nano-aluminum hydroxide gel dry powder with 30g of binder pseudo-boehmite, 2g of dilute nitric acid (mass concentration 17%) and 25g of water, and then shape it in an extruder. The molded product was dried at 100°C for 10 hours, calcined at 240°C for 3 hours, and then calcined at 850°C for 4 hours with a heating rate of 5°C / min to obtain the alumina carrier A2 of the present invention.

[0044] 24g contains MoO 3 Add 82% (weight) ammonium molybdate and 22g nickel nitrate containing 25% (weight) NiO to 100ml ammo...

Embodiment 3

[0047] Under stirring conditions, 548g of aluminum nitrate nonahydrate and 132g of urea were mixed and heated to 70°C, and added to the mixture of 120g of polyisobutylene maleate triethanolamine maleate and 200g of 150HVI neutral oil at the same temperature to form supersolubilizing micelles , and then reacted at 150° C. for 8 hours to obtain nano-aluminum hydroxide gel. Wash three times with 200ml of distilled water, and dry at 120°C for 10 hours. Mix 90g of nano-aluminum hydroxide gel dry powder with 10g of binder pseudo-boehmite, 1.5g of hydrochloric acid, and 15g of water, and then shape it in an extruder. The molded product was dried at 100°C for 10 hours, calcined at 240°C for 3 hours, and then calcined at 850°C for 4 hours with a heating rate of 5°C / min to obtain the alumina carrier A3 of the present invention.

[0048] 162g contains MoO 3 Add 82% (weight) ammonium molybdate and 120g cobalt nitrate containing 25% (weight) CoO to 500ml ammonia water of 35% (weight), di...

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Abstract

The invention discloses a hydrotreating catalyst and a preparation method thereof. The hydrotreating catalyst comprises an alumina carrier and active metal components, wherein the active metal components are loaded onto the carrier by utilizing a traditional immersion method, and when the active metal components are loaded onto the surface of the carrier uniformly, and active metal micelles prepared by a super-solubility micelle method are partially introduced into the carrier, thus clubbed oxides are reserved in the large pore paths (especially channels with diameters over 60 nm) of the alumina carrier. The broad spaces of the large pore paths are fully utilized, therefore the catalyst have a significantly improved capacity of removing metallic impurities from residual oil.

Description

technical field [0001] The invention relates to a hydrogenation treatment catalyst and a preparation method thereof, in particular to a hydrogenation treatment catalyst used for residual oil and other macromolecule-containing reactants or products and a preparation method thereof. Background technique [0002] So far, the catalyst carrier used in the fixed bed of residual oil is still the classic alumina carrier. High temperature calcination method, pH value swing method and water vapor treatment can all obtain macroporous alumina suitable for residual oil, the pore volume of which is concentrated at 8-15nm can reach more than 80%, and the catalyst has high initial activity. The pores of macroporous alumina are continuous through the residual oil molecules, but the pores are too concentrated at about 10nm-20nm, which is not conducive to the long-term operation of the catalyst. The blockage of the catalyst bed causes the shutdown of the device and the replacement of the cata...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J35/02B01J32/00B01J37/02B01J23/882B01J23/883C10G45/04C10G45/08B01J35/00
Inventor 王鼎聪
Owner CHINA PETROLEUM & CHEM CORP
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