Ethylene polymerization method and polyethylene
A technology of ethylene polymerization and polymerization reaction, which is applied in the field of polyethylene, can solve the problems of poor thermal stability and hydrothermal stability, low ethylene polymerization activity, and affect the loading effect, etc., achieve stable mesopore structure, good fluidity, and reduce production cost effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0029] In a preferred case, the preparation method of the catalyst may include: contacting the spherical illite mesoporous composite material with a mother liquor containing magnesium salt and / or titanium salt in the presence of an inert gas.
[0030] Preferably, the contacting conditions include: a temperature of 25-100° C., preferably 40-60° C.; a time of 0.1-5 h, preferably 1-3 h.
[0031] The mother liquor that contains magnesium salt and / or titanium salt can be the organic solvent that contains magnesium salt and / or titanium salt, and described organic solvent can be Virahol and tetrahydrofuran, and the volume ratio of tetrahydrofuran and Virahol can be 1: 1-3, preferably 1:1-1.5.
[0032]During the preparation of the catalyst, the amount of the magnesium salt and / or the titanium salt is preferably in excess relative to the spherical illite mesoporous composite material. More preferably, the amount of the magnesium salt, the titanium salt and the spherical illite mesopor...
Embodiment approach
[0047] In the present invention, the conditions of the first mixed contact include: the temperature may be 10-60°C, preferably 25-60°C; the time may be 10-72 hours, preferably 10-30 hours; the pH value is 1- 7, preferably 3-6. In order to be more conducive to uniform mixing among the various substances, according to a preferred embodiment of the present invention, the first mixing and contacting is performed under stirring conditions.
[0048] In the present invention, the crystallization conditions include: the temperature may be 30-150° C., preferably 90-150° C.; the time may be 10-72 hours, preferably 10-40 hours. According to a preferred embodiment, the crystallization is carried out by hydrothermal crystallization.
[0049] In the present invention, in the process of preparing the filter cake of the mesoporous molecular sieve material having a three-dimensional cubic cage-like pore structure, the process of obtaining the filter cake by filtering may include: washing afte...
Embodiment 1
[0082] This example is used to illustrate the ethylene polymerization method and the obtained polyethylene of the present invention.
[0083] (1) Preparation of spherical illite mesoporous composites
[0084] With 1.46g (0.0001mol) template F108, 5.24g (0.03mol) of K 2 SO 4 Stir with 60g of hydrochloric acid solution with a normality of 2 (2N) at 38°C until F108 is completely dissolved;
[0085] Add 4.2g (0.02mol) of tetraethyl orthosilicate to the above solution, stir at 38°C for 15 minutes, and stand at 38°C for 24 hours;
[0086] Then it was transferred to an agate-lined reaction kettle, crystallized at 100°C for 24 hours, then filtered and washed 4 times with deionized water, and dried to obtain the original powder mesoporous material; the original powder mesoporous material was washed with ethanol Reflux washing at 78° C. for 24 hours, and then suction filtration to obtain a filter cake A1 of mesoporous molecular sieve material with a three-dimensional cubic cage-like ...
PUM
Property | Measurement | Unit |
---|---|---|
Bulk density | aaaaa | aaaaa |
Melt index | aaaaa | aaaaa |
Bulk density | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information

- Generate Ideas
- 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