Process for Olefin Polymerization
A technology for polyolefins and olefin monomers, applied in the field of reaction systems, can solve problems such as limiting maximum productivity, and achieve the effect of improving operability and continuity
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[0213] The following examples show that controlling catalyst activity in the expansion section (by adding thermal runaway reducing agents) results in a more homogeneous product.
[0214] The inventors believe that the reason for obtaining a more homogeneous product is the control of the temperature in the expansion section due to the control of the catalyst activity.
[0215] The present invention relates to the cooling of the expansion section by taking part of the cooled recycle stream and adding it to the expansion section. It is expected that this will also control the temperature in the expansion section. Accordingly, the inventors believe that by withdrawing a liquid-containing stream from a portion of the cooled recycle stream, introducing said liquid-containing stream into the expansion section during at least part of the polymerization process, and causing said liquid-containing stream to Contact with at least a portion of the inner surface of the expanded section wi...
example 1
[0220] Example 1. TRRA is PEEB
[0221] The polymerization catalyst was prepared as follows:
[0222] Example 1: Preparation of procatalyst on activated butyl-Grignard support.
[0223] Preparation of Grignard reagent (step o)) - stage A
[0224] This step o) constitutes the first part of stage A of the process for preparing the procatalyst.
[0225] A stirred flask equipped with a reflux condenser and funnel was charged with magnesium powder (24.3 g). Place the flask under nitrogen. Magnesium was heated at 80°C for 1 hour, after which dibutyl ether (150ml), iodine (0.03g) and n-chlorobutane (4ml) were added sequentially. After the color of iodine disappeared, the temperature was raised to 80° C. and a mixture of n-chlorobutane (110 ml) and dibutyl ether (750 ml) was added slowly for 2.5 hours. The reaction mixture was stirred for a further 3 hours at 80°C. Stirring and heating were then discontinued and a small amount of solid material was allowed to settle for 24 h...
example 2
[0272] C-donor means: cyclohexylmethyldimethoxysilane.
[0273] N-donor means: n-Propyltrimethoxysilane
[0274] The polymerization catalyst was prepared as described in Example-1. Similar procedures and equipment used in Example-1 were used in this example for molecular weight distribution (MWD) using GPC and crystallinity using ATREF.
[0275] The effect of different TRRA / Si ratios on yield for both TA and DB is shown in Table 4 below:
[0276] Table 4. Yield versus TRRA / Si molar ratio for TA and DB at 67°C and 82°C.
[0277]
[0278]Table 4 shows the yield for TA at different molar ratios of TRRA to electron donor (TRRA / Si). The addition of TA showed almost similar degrees of inactivation at both temperatures, where when benchmarked with zero TA at 67°C, the activity drops were −43% and −67% at 67°C and 82°C, respectively . Therefore, TA is preferably used as one of the components in a mixture with another TRRA. Table 4 also shows the yield for DB at different mola...
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Abstract
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