A kind of ethylene polymerization method and polyethylene
An ethylene polymerization and polymerization reaction technology, applied in the field of polyethylene, can solve the problems of poor thermal stability and hydrothermal stability, low ethylene polymerization activity, collapse of pore walls, etc., and achieve stable mesoporous structure, high catalytic activity, and low melting point. The effect of the index
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0026] In a preferred case, the preparation method of the catalyst may include: in the presence of an inert gas, impregnating the spherical zeolite mesoporous composite material in a mother liquor containing magnesium salt and / or titanium salt, followed by filtering and drying in sequence.
[0027] According to the present invention, the impregnating conditions may include: a temperature of 25-100° C., and a time of 0.1-5 hours; preferably, the impregnating conditions include: a temperature of 40-60° C., and a time of 1-3 hours.
[0028]In the present invention, the amount of the magnesium salt and the titanium salt is not particularly limited, and preferably, the amount of the carrier, the magnesium salt, and the titanium salt is such that in the prepared catalyst, the total amount of the catalyst is Based on weight, the content of the spherical zeolite mesoporous composite material is 90-99% by weight, and the sum of the contents of the magnesium salt and titanium salt in ter...
Embodiment 1
[0086] This example is used to illustrate the ethylene polymerization method and the obtained polyethylene of the present invention.
[0087] (1) Preparation of spherical zeolite mesoporous composites
[0088] 1.46g (0.0001mol) template agent F108, 5.24g (0.03mol) K 2 SO 4 Stir with 60g of hydrochloric acid solution with a normality of 2 at 38°C until F108 is completely dissolved;
[0089] Add 4.2g (0.02mol) tetraethyl orthosilicate to the above solution, stir at 38°C for 15 minutes, and stand at 38°C for 24 hours;
[0090] Then it was transferred to an agate-lined reactor, crystallized at 100°C for 24 hours, then filtered and washed 4 times with deionized water, and then suction filtered to obtain a mesoporous molecular sieve material with a three-dimensional cubic cage-like channel structure. Filter cake A1.
[0091] The water glass with a concentration of 15% by weight and the sulfuric acid solution and glycerin with a concentration of 12% by weight are mixed in a weigh...
Embodiment 2
[0107] This example is used to illustrate the ethylene polymerization method and the obtained polyethylene of the present invention.
[0108] (1) Preparation of spherical zeolite mesoporous composites
[0109] 1.46g (0.0001mol) template agent F108, 6.96g (0.04mol) K 2 SO 4 Stir with 60g of hydrochloric acid solution with a normality of 2 at 38°C until F108 is completely dissolved;
[0110] Add 3.1g (0.015mol) tetraethyl orthosilicate to the above solution, stir at 45°C for 15min, and stand at 45°C for 30h;
[0111] Then it was transferred to an agate-lined reactor, crystallized at 120°C for 30 hours, then filtered and washed 4 times with deionized water, and then suction filtered to obtain a mesoporous molecular sieve material with a three-dimensional cubic cage-like channel structure. Filter cake A2.
[0112] Concentration is 20% by weight of water glass and concentration of 12% by weight of sulfuric acid solution and glycerol mixed with a weight ratio of 4:1:1 and contact ...
PUM
Property | Measurement | Unit |
---|---|---|
particle size | aaaaa | aaaaa |
specific surface area | aaaaa | aaaaa |
melt flow index | 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