Catalyst for synthesizing cyclohexylbenzene
A cyclohexylbenzene and catalyst technology, which is applied in molecular sieve catalysts, physical/chemical process catalysts, organic chemistry, etc., can solve the problem of low selectivity of cyclohexylbenzene, high selectivity of by-product methylcyclopentylbenzene, phenol cyclohexylbenzene Difficult separation of ketone products and other problems to achieve the effect of improving selectivity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0040] 1. Catalyst preparation
[0041] Weigh PdCl containing Pd1.5g 2 Be dissolved in 1mol / L hydrochloric acid aqueous solution and be made into 80g solution I; Take by weighing 100g diameter be 1mm, the non-bonding cylindrical hydrogen type BEA zeolite molecular sieve of length 5mm (the mol ratio of silicon dioxide / aluminum oxide is 45); The solution I was loaded on the hydrogen-type BEA zeolite molecular sieve, impregnated at room temperature for 12 hours, dried at 100° C. for 12 hours, and calcined at 450° C. for 4 hours to prepare the desired catalyst.
[0042] 2. Catalyst evaluation
[0043] Get 10ml catalyst packing in the fixed-bed reactor, carry out activity evaluation after reduction activation, condition is as follows: the temperature of reaction is 150 ℃, and the mol ratio of benzene and hydrogen in the reaction raw material is 0.8, and the pressure of reaction is 2.0MPa (gauge pressure) , the weight space velocity of the raw material benzene for the reaction is ...
Embodiment 2
[0070] 1. Catalyst preparation
[0071] Weigh PdCl containing 0.3gPd 2 Dissolve in 1mol / L hydrochloric acid aqueous solution and be made into 40g solution I; Weigh the La(NO 3 ) 3 ·6H 2 O is dissolved in water to make 20g solution II; weigh Co(NO 3 ) 3 ·6H 2 O is dissolved in water and made into 20g solution III; then solution I, solution II and solution III are mixed uniformly; 100g diameter is taken by weighing 1mm, length 5mm cylindrical hydrogen-type BEA zeolite molecular sieve (silicon dioxide / oxidized The molar ratio of aluminum is 45), the mixed solution is loaded on the hydrogen-type BEA zeolite molecular sieve, impregnated at room temperature for 12 hours, dried at 100°C for 12 hours, and calcined at 450°C for 4 hours to prepare the desired catalyst.
[0072] 2. Catalyst evaluation
[0073] Catalyst evaluation method see embodiment 1.
[0074] For the convenience of comparison, the composition of the catalyst is listed in Table 1, and the evaluation results ar...
Embodiment 3
[0076] 1. Catalyst preparation
[0077] Weigh PdCl containing 0.3gPd 2 Be dissolved in 1mol / L hydrochloric acid aqueous solution and be made into 40g solution I; Take the Ce(NO 3 ) 3 ·6H 2 O is dissolved in water to make 20g solution II; weigh Co(NO 3 ) 3 ·6H 2 O is dissolved in water and made into 20g solution III; then solution I, solution II and solution III are mixed uniformly; 100g diameter is taken by weighing 1mm, length 5mm cylindrical hydrogen-type BEA zeolite molecular sieve (silicon dioxide / oxidized The molar ratio of aluminum is 45), the mixed solution is loaded on the hydrogen-type BEA zeolite molecular sieve, impregnated at room temperature for 12 hours, dried at 100°C for 12 hours, and calcined at 450°C for 4 hours to prepare the desired catalyst.
[0078] 2. Catalyst evaluation
[0079] Catalyst evaluation method see embodiment 1.
[0080] For the convenience of comparison, the composition of the catalyst is listed in Table 1, and the evaluation results...
PUM
Login to View More 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
