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Polymerization of isobutylene catalyzed by EtAlCl2/bis(2-chloroethyl) ether complex in steel vessels
被引:24
作者:
Banerjee, Sanjib
[1
]
Emert, Jack
[2
]
Wright, Peter
[2
]
Skourlis, Thomas
[2
]
Severt, Rich
[2
]
Faust, Rudolf
[1
]
机构:
[1] Univ Massachusetts, Dept Chem, Lowell, MA 01854 USA
[2] Infineum USA, Linden, NJ 07036 USA
关键词:
HIGHLY REACTIVE POLYISOBUTYLENE;
OLEFIN-TERMINATED POLYISOBUTYLENE;
WEAKLY COORDINATING ANIONS;
CATIONIC-POLYMERIZATION;
MANGANESE(II) COMPLEXES;
LIVING POLYISOBUTYLENE;
FECL3/ETHER COMPLEXES;
ROOM-TEMPERATURE;
MECHANISM;
ANHYDRIDE;
D O I:
10.1039/c5py00624d
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
When synthesis of highly reactive polyisobutylene (HR PIB) via cationic polymerization of isobutylene (IB) using ethylaluminum dichloride.bis(2-chloroethyl) ether (EADC.CEE) complex were carried out in metal reactors made of 316 stainless steel (SS), PIB olefin with up to 20% lower exo-olefin content were obtained compared to that obtained in glass reactors (up to 90%). In an effort to investigate this reduction in exo-olefin selectivity in SS reactors, we have studied the polymerization of IB using EADC.CEE complex in SS (minimum of 10.5% chromium content by mass), carbon steel (CS) (0% chromium content by mass), monel alloy 400 (M400) (0% chromium content by mass) and glass reactors. The latter was examined in the presence and absence of SS balls. Mechanistic studies using ATR-FTIR and H-1 NMR spectroscopy suggest that this decrease in exo-olefin selectivity is due to a side reaction of EADC with Cr2O3 involving the loss of the ethyl group from EADC and decomplexation of the EADC.CEE complex which hinders the selective abstraction of the beta-proton from the growing chain end. In the absence of chromium (CS and M400 reactors), the exo-olefin content is virtually identical to that obtained in glass reactors. Therefore, CS and M400 reactors are suitable to produce HR PIB with high exo-olefin content.
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页码:4902 / 4910
页数:9
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