A kind of supported catalyst and its preparation method, the method for catalytic synthesis of n-ethylaniline
A supported catalyst and catalyst technology, applied in the field of catalysis, can solve problems such as low selectivity of N-ethylaniline, and achieve the effects of high selectivity, improved selectivity and improved catalytic efficiency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0033] The present invention also provides a preparation method of the supported catalyst described in the above technical scheme, comprising the following steps:
[0034] Soluble Cu salt, organic solvent and Al 2 o 3 After mixing, dry to obtain solid product;
[0035] After mixing the solid product, tetraethyl silicate and ethanol, mixing with an alkaline pH regulator, and adjusting the pH value, a catalyst precursor is obtained;
[0036] The catalyst precursor is calcined to obtain the supported catalyst.
[0037] In the present invention, unless otherwise specified, the raw materials used are conventional commercially available products in this field.
[0038] The present invention combines soluble Cu salt, organic solvent and Al 2 o 3 After mixing, drying afforded a solid product.
[0039] In the present invention, the soluble Cu salt preferably includes one or more of copper nitrate, copper acetate and copper chloride. In the present invention, the organic solvent ...
Embodiment 1
[0059] Take by weighing 241mg copper nitrate trihydrate (1mmol), join in 128g acetone, after stirring and dissolving in the round bottom flask, weigh 128gAl 2 o 3 Add it into a round bottom flask, stir at 35°C for 12h until the acetone evaporates, then dry at 120°C for 3h to obtain a solid product;
[0060] Mix 1.6g tetraethyl silicate and 198mL ethanol to obtain a tetraethyl silicate ethanol solution with a mass concentration of 1.0wt%, add the obtained solid product to the tetraethyl silicate ethanol solution, and stir thoroughly Finally, add ammonia water dropwise, adjust to pH=7.5, make tetraethyl silicate hydrolyze completely, the drip rate of ammonia water is 1mL / min, in Cu(OH) 2 / Al 2 o 3 Surface precipitation forms SiO 2 Thin film, obtain catalyst precursor;
[0061] The obtained catalyst precursors were washed with water in turn until neutral, filtered, and the filter residue was dried at 120°C for 3 hours, then placed in a muffle furnace, heated from room temper...
Embodiment 2
[0065] Take by weighing 400mg copper acetate (2mmol), join in 128g acetone, after stirring and dissolving in the round bottom flask, weigh 128gAl 2 o 3 Add it into a round bottom flask, stir at 35°C for 8h until the acetone volatilizes, then dry at 120°C for 3h to obtain a solid product;
[0066] Mix 3.2g tetraethyl silicate and 196mL ethanol to obtain a tetraethyl silicate ethanol solution with a mass concentration of 2.0wt%, add the obtained solid product to the tetraethyl silicate ethanol solution, and stir thoroughly Finally, add ammonia water dropwise, adjust to pH=7.5, make tetraethyl silicate hydrolyze completely, the drip rate of ammonia water is 1mL / min, in Cu(OH) 2 / Al 2 o 3 Surface precipitation forms SiO 2 Thin film, obtain catalyst precursor;
[0067] The obtained catalyst precursors were washed with water in sequence to neutrality, filtered, and the filter residue was dried at 120°C for 3 hours, then placed in a muffle furnace, heated from room temperature t...
PUM
Property | Measurement | Unit |
---|---|---|
specific surface area | aaaaa | aaaaa |
boiling point | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com