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
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
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...
PUM
| Property | Measurement | Unit |
|---|---|---|
| diameter | aaaaa | aaaaa |
| diameter | aaaaa | aaaaa |
| specific surface area | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com
