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HRID 8389作成日:2026年10月25日

Ethylene → Ethene;oct-1-ene

https://huagongshe.com/reaction/8389

反応式

関与物質

役割名称HCID仕込み量
反応物EthyleneHCID 6325—
反応物1-OcteneHCID 8125—
反応物EthylidenenorborneneHCID 27756—
反応物Methyldi(octadecyl)ammonium tetrakis(pentafluorophenyl)borateHCID 10876944—
反応物HCID 178418361HCID 178418361—
溶媒TolueneHCID 1140—
生成物Ethene;oct-1-eneHCID 168495—

反応条件

温度130 °C

反応手順

All liquids except ethylidenenorbornene (ENB) and gas feeds were passed through columns of alumina and a decontaminant (Q-5™ catalyst available from Englehardt Chemicals Inc.) prior to introduction into the reactor. ENB was passed through a short column (3×10 cm) of alumina prior to introduction to the reactor. Catalyst components are handled in a glovebox containing an atmosphere of argon or nitrogen. A stirred 2.0 liter reactor is charged with 640 g of mixed alkanes solvent, 150 g of 1-octene and 16 g of ENB. Hydrogen (20 psi, 140 kPa) is added as a molecular weight control agent by differential pressure expansion from a 75 mL addition tank. The reactor is heated to 100° C. and saturated with ethylene at 500 psig (3.5 MPa). Metal complex as dilute toluene solution and cocatalyst as dilute solutions in toluene were mixed in a 1:1 molar ratio and transferred to a catalyst addition tank and injected into the reactor. The cocatalyst was methyldi(octadecyl)-ammonium tetrakis(pentafluoro-phenyl)borate (DAB), the ammonium cation of which is derived from a mixture of amines available commercially as methyl bis(tallow)amine. The polymerization conditions were maintained for 15 minutes with ethylene added on demand. The resulting solution was removed from the reactor, quenched with isopropyl alcohol, and stabilized by addition of a toluene solution containing 67 mg/100 g polymer of a hindered phenol antioxidant (Irganox™ 1010 from Ciba Geigy Corporation) and 133 mg/100 g polymer of a phosphorus stabilizer (Irgafos™ 168 from Ciba Geigy Corporation). Between sequential polymerization runs, a wash cycle was conducted in which 850 g of mixed alkanes was added to the reactor and the reactor was heated to 130° C. The reactor was then emptied of the heated solvent immediately before beginning a new polymerization run.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087773B2
出典データセットuspto-grants-2006_08
ORD IDord-3c74f0dae9174e5a9b948560c4277649
出典メモuspto-grants-2006_08