Ethylene/1-butene copolymer having excellent processability
A technology of butene copolymer and butene copolymerization is applied in the field of ethylene/1-butene copolymer, which can solve the problems of deterioration of long-term pressure resistance, deterioration of brittle fracture mode resistance, and inability to satisfy physical properties and processability of products at the same time. , to achieve the effect of improving processability and excellent stress cracking resistance
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[0117] The preparation example of the first metallocene compound
[0118] Synthetic Example 1: [(tBu-O-(CH 2 ) 6 )(CH 3 )Si(C 5 (CH 3 ) 4 )(tBu-N)TiCl 2 ] preparation
[0119] 50 g of Mg was put into a 10 L reactor at room temperature, and then 300 mL of THF was added thereto. Add about 0.5g of I 2 Afterwards, the reactor temperature was maintained at 50 °C. After the reactor temperature was stabilized, 250 g of 6-tert-butoxyhexyl chloride was added to the reactor at a rate of 5 mL / min using a feed pump. An increase in reactor temperature of approximately 4°C to 5°C was observed with the addition of 6-tert-butoxyhexyl chloride. 6-tert-butoxyhexyl chloride was added continuously with stirring over 12 hours. After reacting for 12 hours, a black reaction solution was obtained. After sampling 2 mL of the resulting black solution, water was added thereto to obtain an organic layer. Therefore, by 1 H-NMR identified 6-tert-butoxyhexane. 6-tert-butoxyhexane in...
preparation Embodiment 1
[0138] 3.0 kg of toluene solution was put into a 20 L stainless steel (sus) high pressure reactor, and the temperature of the reactor was kept at 40°C. 500 g of silica (Grace Davison, SP2212) dehydrated under vacuum at 600° C. for 12 hours was added to the reactor and dispersed well. Then, 2.78 kg of a 10% by weight methylaluminoxane (MAO) / toluene solution was added, followed by stirring at 80° C. and 200 rpm for more than 15 hours.
[0139]The temperature of the reactor was lowered to 40° C., and then 200 g of a 7.8% by weight metallocene compound / toluene solution of Synthesis Example 1 was added to the reactor, followed by stirring at 200 rpm for 1 hour. Subsequently, 250 g of an 8.7% by weight metallocene compound / toluene solution of Synthesis Example 2 was added to the reactor, followed by stirring at 200 rpm for 1 hour.
[0140] 70 g of co-catalyst (anilinium tetrakis(pentafluorophenyl)borate) diluted in toluene was added to the reactor, followed by stirring at 200 rpm f...
preparation Embodiment 2
[0143] A supported catalyst was prepared in the same manner as in Preparation Example 1 except that 125 g of the metallocene compound / toluene solution of Synthesis Example 1 was added in Preparation Example 1.
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