Supported late-transition-metal catalyst used for ethylene polymerization and preparation method thereof and application thereof
A late transition metal and ethylene polymerization technology, which is applied in the field of preparation of supported late transition metal catalysts, can solve the problems of limited industrial application, uncontrollable, poor carrier particle shape, etc.
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Embodiment 1
[0067] (1) Preparation of chlorinated hydrocarbyl silicon / magnesium chloride support
[0068] Under the protection of nitrogen, take 10.0 g of magnesium chloride carrier and put it into a glass reactor, add 100 ml of dried hexane, disperse into a suspension, add 1 ml of SiCl 2 (n-Bu) 2 , start stirring, heat up to 30° C., react for 4 hours, and dry in vacuum to obtain a solid powder with good fluidity.
[0069] (2) Preparation of organoaluminum / hydrocarbyl chloride / magnesium chloride carrier
[0070] Under nitrogen protection, take 5.0 grams of the modified magnesium chloride carrier obtained above and add it to a glass reactor, add 60 milliliters of dried toluene, disperse into a suspension, and add 18 milliliters of 10 wt% MAO (methylaluminoxane) toluene solution , heated to 50 ° C, stirred for 4 hours, then washed three times with 50 ml × 3 toluene, then washed with hexane, and dried in vacuum to obtain a solid powder with good fluidity, that is, a magnesium chloride carr...
Embodiment 2
[0080] (1) Preparation of chlorinated hydrocarbyl silicon / silica gel support
[0081] With embodiment 1 step (1), only SiCl in embodiment 1 2 (n-Bu) 2 Change to SiCl 4 .
[0082] (2) Preparation of organoaluminum / hydrocarbyl chloride / magnesium chloride carrier
[0083] Same as step (2) of Example 1.
[0084] (3) Preparation of supported transition metal catalyst B
[0085] Same as step (3) of Example 1, only 0.096 grams of [(2,6-bis[1-(2,4,6-trimethylbenimine) ethyl]pyridine ferric dichloride] in Example 1 Replaced with 0.111 grams of [(2,6-bis[1-(2,6-diisopropylphenylimine) ethyl]pyridine ferric dichloride] (see below for its structure, see patent WO9827124A1 for its synthesis, examples 8) to obtain the supported transition metal catalyst B. Characterized by ICP, the weight content of Fe in catalyst B is 0.22%, and the weight content of Al is 11.41%.
[0086]
Embodiment 3
[0088] (1) Preparation of chlorinated hydrocarbyl silicon / silica gel support
[0089] Same as (1) preparation method in Example 1.
[0090] (2) Preparation of organoaluminum / hydrocarbyl chloride / magnesium chloride carrier
[0091] Same as step (2) of Example 1, only 18 ml of 10% MAO was replaced with 13 ml of 2M diethylaluminum chloride.
[0092] (3) Preparation of supported transition metal catalyst C
[0093] Same as step (3) of Example 1, only 0.096 grams of [(2,6-bis[1-(2,4,6-trimethylbenimine) ethyl]pyridine ferric dichloride] in Example 1 Replaced with 0.098 g [(2,6-bis[1-(2-methyl 6-chloro-phenylimine) ethyl]pyridine ferric dichloride] (see below for its structure, see patent WO9827124A1 for its synthesis, examples 2) The supported transition metal catalyst C was obtained. Characterized by ICP, the weight content of Fe in catalyst C was 0.20%, and the weight content of Al was 11.92%.
[0094]
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