CN1065881C - Catalyst for preparing block copolymer of syndiotactic polystyrene and polyethylene - Google Patents
Catalyst for preparing block copolymer of syndiotactic polystyrene and polyethylene Download PDFInfo
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- CN1065881C CN1065881C CN98110751A CN98110751A CN1065881C CN 1065881 C CN1065881 C CN 1065881C CN 98110751 A CN98110751 A CN 98110751A CN 98110751 A CN98110751 A CN 98110751A CN 1065881 C CN1065881 C CN 1065881C
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- Prior art keywords
- syndiotactic polystyrene
- polyethylene
- catalyst
- titanium compound
- alkylaluminoxane
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- 229920010524 Syndiotactic polystyrene Polymers 0.000 title claims abstract description 14
- -1 polyethylene Polymers 0.000 title claims abstract description 14
- 239000004698 Polyethylene Substances 0.000 title claims abstract description 10
- 229920000573 polyethylene Polymers 0.000 title claims abstract description 10
- 239000003054 catalyst Substances 0.000 title abstract description 5
- 229920001400 block copolymer Polymers 0.000 title 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims abstract description 9
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims abstract description 9
- 150000003609 titanium compounds Chemical class 0.000 claims abstract description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 14
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 239000004411 aluminium Substances 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052751 metal Inorganic materials 0.000 claims description 2
- 239000002184 metal Substances 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 230000003197 catalytic effect Effects 0.000 abstract description 9
- 229920000642 polymer Polymers 0.000 abstract description 7
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 abstract 1
- 125000005234 alkyl aluminium group Chemical group 0.000 abstract 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 abstract 1
- 238000009776 industrial production Methods 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 30
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 26
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 13
- 229910052757 nitrogen Inorganic materials 0.000 description 13
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 11
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- CPOFMOWDMVWCLF-UHFFFAOYSA-N methyl(oxo)alumane Chemical compound C[Al]=O CPOFMOWDMVWCLF-UHFFFAOYSA-N 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 239000010936 titanium Substances 0.000 description 8
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- MCJUWBUSIQXMPY-UHFFFAOYSA-N cyclopenta-1,3-diene titanium Chemical compound [Ti].C1C=CC=C1 MCJUWBUSIQXMPY-UHFFFAOYSA-N 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000007334 copolymerization reaction Methods 0.000 description 4
- 210000004940 nucleus Anatomy 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 229910052719 titanium Inorganic materials 0.000 description 4
- 238000001291 vacuum drying Methods 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 3
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 239000002250 absorbent Substances 0.000 description 2
- 230000002745 absorbent Effects 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical group 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 238000002329 infrared spectrum Methods 0.000 description 2
- 229910017053 inorganic salt Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000001819 mass spectrum Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 2
- 238000012856 packing Methods 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000012661 block copolymerization Methods 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 238000001460 carbon-13 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 150000002240 furans Chemical class 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 210000003097 mucus Anatomy 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- VYNCPPVQAZGELS-UHFFFAOYSA-N toluene;trimethylalumane Chemical compound C[Al](C)C.CC1=CC=CC=C1 VYNCPPVQAZGELS-UHFFFAOYSA-N 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Abstract
The present invention relates to a catalyst used for preparing a block polymer (PE-b-sPS) of syndiotactic polystyrene and polyethylene, which comprises an organic metallic titanium compound CpTi(OCH2R1)3 and alkylaluminium oxane, wherein Cp is cyclopentadienyl, and R1 is an aromatic heterocyclic group containing 4 to 20 carbon atoms. With the characteristics of high catalytic activity and high catalytic efficiency, the catalyst can be used in industrial production.
Description
The present invention relates to be used to prepare the catalyzer of syndiotactic polystyrene and polyethylene block multipolymer.
Styrene polymer can be divided into random polystyrene, isotactic polyphenylacetylene and syndiotactic polystyrene.The catalyzer that synthesis of syndiotactic polystyrene adopts organo-metallic titanium compound and poly-methylaluminoxane (MAO) to form usually.The organo-metallic titanium compound is mainly cyclopentadiene titanium compound.EP210615 and US5252693 etc. have reported employing CpTiCl
3/ MAO catalyzer is used for the situation of syndiotactic polymerization of phenylethylene, but its catalytic activity and catalytic efficiency are not high, and is industrial undesirable, and this catalyzer also is not suitable for being used for the block copolymerization of vinylbenzene and ethene simultaneously.
The purpose of this invention is to provide a kind of new preparation syndiotactic polystyrene and the catalyzer of polyethylene block multipolymer, this catalyzer has high catalytic activity and catalytic efficiency.
The objective of the invention is to realize by following technical scheme: a kind of catalyzer for preparing syndiotactic polystyrene and polyethylene block multipolymer comprises organic metal titanium compound I and alkylaluminoxane II;
CpTi(OCH
2R
1)
3 Ⅰ
Cp is a cyclopentadienyl in the formula;
R
1Be furan group;
R
2For containing the alkyl of 1~4 carbon atom;
N is the oligomerisation degree of alkylaluminoxane, and its value is 6~40;
Aluminium is 50~2000 to the molar ratio range of organo-metallic titanium compound I in the alkylaluminoxane II.
R in the technique scheme
2Preferred version be methyl, the value preferable range of oligomerisation degree n is 10~30.
Poly-alkylaluminoxane (MAO) is that the control hydrolysis by aluminum alkyls prepares, and reactants water can be the water that contains in the inorganic salt of crystal water, and the inorganic salt that contain crystal water can be CaCl
26H2
O, MgCl
26H
2O, CuSO
45H
2O, Al
2(SO
4)
318H
2O, CaSO
42H
2O, MgSO
47H
2O, FeSO
47H
2O, Ti (SO
4)
24H
2O, Ti
2(SO
4)
38H
2O and ZnSO
47H
2O etc.The mole ratio of trimethyl aluminium and water is 1: 1~3.0, and temperature of reaction is-20~100 ℃, and the reaction times is 10~40 hours.Aluminum alkyls commonly used has trimethyl aluminium, triethyl aluminum, triisobutyl aluminium etc.Concrete steps are: aluminum alkyls is pressed Al/H
2The O mol ratio is 1: 1~2.5 slowly to be added dropwise to Al under-20~0 ℃
2(SO
4)
318H
2In the toluene solution of O, the dropping time is 0.5~5 hour; After dropwising, make temperature of reaction rise to 20~100 ℃, under this temperature, reacted 5~40 hours, after reaction finished, with solid filtering, evaporation removed to desolvate and obtains white solid product, promptly obtains the alkylaluminoxane that structure is an II.The preparation method of cyclopentadiene titanium compound I is as follows: by corresponding cyclopentadienyl titanous chloride and furfuryl alcohol (HO
) in the presence of chlorine hydride absorbent, be that solvent reaction makes with the hydrocarbon polymer.Chlorine hydride absorbent can be various aminated compoundss, wherein is advisable with trialkylamine, for example triethylamine.Hydrocarbon polymer can be aliphatic hydrocarbon or aromatic hydrocarbon, uses aromatic hydrocarbon better, for example benzene, toluene etc.Concrete steps are: ethamine and furfuryl alcohol mixing solutions are slowly dropped in the benzole soln of cyclopentadienyl titanous chloride, the mole ratio of cyclopentadienyl titanous chloride and furfuryl alcohol is 1: 3.0~3.5, the mole ratio of cyclopentadienyl titanous chloride and triethylamine is 1: 3.0~3.5, temperature of reaction is 0~60 ℃, and the reaction times is 1~30 hour, solids removed by filtration, underpressure distillation removes and desolvates, the crude product hexane extraction that obtains, remove volatile matter after, jonquilleous mucus.
Work as R
1During for furyl, the ultimate analysis of chemical compounds I, hydrogen nuclear magnetic resonance spectrum
1HNMR, nuclear magnetic resonance of carbon spectrum
13CNMR, mass spectrum MS and infrared spectra the results are shown in following data:
Ultimate analysis (element analyses)
Calcd?for?C
20H
20O
6Ti:C:59.42;H:4.99。Found:C:59.84;H:4.64
Hydrogen nuclear magnetic resonance spectrum [
1HNMR (CDCl
3TMS intern)]:
δ5.10(s,6H,(OCH
2)
3),6.20-6.28(m,9H,(CCHCHCHO)
3),
6.32-6.36(m,5H,Cp?H)。
Carbon
13Nuclear magnetic resonance spectrum [
13CNMR (CDCCl
3)]:
δ69.8(OCH
2),154.6(C),110.0(CH-CH),106.9(CH=CH-O),141.4(CH-O),
113.9-114.2(Cp?C)。
Mass spectrum [MS (m/z, %intensity)]:
39(100,CH
2CCH
+),53(70,CH
2CCH
2CH
+),69(40,OCH
2CCHO
+),
81(75,CH
2CHCHCHO
+?or?OTiO
+),95(40,OTiOCH
2 +),98(74,OCH
2CCHCHCHO
+)
112(10,CpTi
+),129(3,CpTiO
+),169(5,M-(OCH
2CCHCHCHO)-(OCCHCHCH)
+),
339(5,M-Cp
+)。
Infrared spectra (Infrared FTIR)
The wave number vibration
3114 luxuriant ring C-H stretching vibrations, furan nucleus=C-H stretching vibration
The hydrocarbon key asymmetrical stretching vibration [VasC-H (O-CH of 2903-2846
2-C)]
1602-1503 furan nucleus skeletal vibration
Near the general frequency absorption band of luxuriant ring 1735
1447 luxuriant ring skeletal vibrations
Two key stretching vibration (V of 1644 furan nucleuss
C-c)
1068-1096 carbon-oxygen bond stretching vibration [V
C-O (Ti)]
The plain bending of C-H vibration on the 1011 luxuriant rings
The out-of-plane deformation vibration of 913885 furan nucleuss=C-H
The eigen vibration of three adjacent hydrogen on the 814-737 furan nucleus
589 titanium carbon bond stretching vibration (V
Ti-c)
421 titanyl key stretching vibration (V
Ti-o)
Catalyst component I and II can be under protection of inert gas (for example nitrogen, argon gas etc.) under 0~50 ℃, preferably 25 ℃ are carried out pre-mixing.
Polyreaction is preferably carried out between 30~60 ℃ at 25~100 ℃.In order to obtain the polymkeric substance of ideal performance, polymerization need be used the regular hour, and by several hours, preferably 1~10 hour, the ideal polymerization time depended on polymerization temperature, solvent and other polymerizing condition from several minutes.The polyreaction mode can adopt solution polymerization, slurry polymerization and mass polymerization.For solution polymerization and slurry polymerization, the solvent of employing is aliphatic hydrocarbon or aromatic hydrocarbon, as hexane, heptane, hexanaphthene, benzene, toluene etc.The concentration of vinylbenzene in solvent is in 5~100% scopes, and ethylene pressure is in 0.1~1.0MPa scope.
The present invention adopts a kind of new metallocene-titanium metal compound as the Primary Catalysts for preparing syndiotactic polystyrene and polyethylene block multipolymer, makes the higher 11.2 kg of polymer/gram titanium that reached of catalytic efficiency of catalyzer, has obtained effect preferably.
Below just the invention will be further elaborated by embodiment
[embodiment 1]
The preparation of cyclopentadiene titanium compound
With 2.41g (11.0mmol) the cyclopentadienyl titanous chloride exsiccant of packing into; be subjected in the 250ml reaction flask of nitrogen protection; add 50ml exsiccant benzene; again under nitrogen protection with dropping funnel lentamente Dropwise 5 0ml contain 3.34g (33.0mmol; 4.60ml) triethylamine and 3.24g (33.0mmol; 2.86ml) the exsiccant benzole soln of furfuralcohol; be allowed to condition under 18 ℃ the temperature and react 24h; filter; drain solvent, use the n-hexane extraction of 40 ℃ of exsiccant again, constant temperature leaves standstill 2h; supernatant liquid is transferred in the container of dried and clean inflated with nitrogen; drain solvent, get golden yellow oily product 4.08g, yield 92%.The toluene solution that is made into 0.02M is standby.
[embodiment 2]
The preparation of MAO
Be equipped with and add 30 Als of gram in the 500ml reactor of induction stirring through milling
2(SO
4)
318H
2O and 70ml toluene, under-10 ℃ of temperature, dripping 200ml concentration is the trimethyl aluminium toluene solution of 3.1M.Rate of addition is 5 ml/min, drips off in 60 minutes.Improve temperature of reaction then gradually, in 2h, make temperature reach 60 ℃, continue reaction 24h.Reaction mixture is removed solid after filtration, filtrate is taken out 1h with vacuum pump under 20 ℃, remove part toluene, under 30 ℃, take out 1h again, under 40 ℃, volatile matters such as toluene are removed at last, obtained 13.0g white solid MAO, productive rate about 32.5%, after measured, the average oligomerisation degree of methylaluminoxane (MAO) is 18.
[embodiment 3]
The preparation of cyclopentadiene titanium compound
With 2.12g (9.66mmol) the cyclopentadienyl titanous chloride exsiccant of packing into; be subjected in the 250ml reaction flask of nitrogen protection; add 45ml exsiccant benzene; under nitrogen protection, drip 45ml lentamente again and contain 2.93g (28.9mmol with dropping funnel; 4.03ml) triethylamine and 2.83g (28.9mmol; 4.00ml) the exsiccant benzole soln of furfuralcohol; be allowed to condition under 20 ℃ the temperature and react 24h; filter; drain solvent, use the n-hexane extraction of 40 ℃ of exsiccant again, constant temperature leaves standstill 2h; supernatant liquid is transferred in the container of dried and clean inflated with nitrogen; drain solvent, get golden yellow oily product 3.55g, yield 91%.The toluene solution that is made into 0.02M is standby.
[embodiment 4]
To the 250ml there-necked flask vacuum-drying 2h of stirring be housed, inflated with nitrogen is kept malleation, add 20ml toluene, the MAO0.21g of embodiment 2 preparations, the cyclopentadiene titanium compound 0.29ml of embodiment 1 preparation activates 3 minutes down at 65 ℃, takes the nitrogen in the reaction flask away, feed the ethene of 0.213Mpa immediately, and kept this stress reaction 5 minutes, and change the ethene in the bottle into nitrogen again, add the triisobutyl aluminium of the 1M of 1ml immediately, 10ml vinylbenzene, continuation is reacted 2.5h down at 65 ℃, and reaction product is filtered and vacuum-drying after 5% acidic methanol termination, get copolymerization product 4.2g, catalytic efficiency is 11.2 kg of polymer/gram titanium.Copolymerization product obtains multipolymer through 40 ℃ of tetrahydrofuran (THF) extractings.Insolubles is syndiotactic polystyrene and Natene.Dsc analysis shows that the Tg of multipolymer is 91 ℃, and two melting peaks are respectively 265 ℃ and 130 ℃, proves that institute's synthetic multipolymer has the PE-b-sPS segmented copolymer of syndiotactic styrenic chain.
[embodiment 5]
To the 250ml there-necked flask vacuum-drying 2h of stirring be housed, inflated with nitrogen is kept malleation, add 20ml toluene, the MAO0.24g of embodiment 2 preparations, the cyclopentadiene titanium compound 0.35ml of embodiment 3 preparations activates 3 minutes down at 65 ℃, takes the nitrogen in the reaction flask away, feed the ethene of 0.118Mpa immediately, and kept this stress reaction 10 minutes, and change the ethene in the bottle into nitrogen again, add the triisobutyl aluminium of the 1M of 1ml immediately, 10ml vinylbenzene, continuation was reacted 50 minutes down at 65 ℃, and reaction product is filtered and vacuum-drying after 5% acidic methanol termination, get copolymerization product 1.8g, catalytic efficiency 5.4 kg of polymer/gram titanium.Copolymerization product obtains multipolymer through 40 ℃ of tetrahydrofuran (THF) extractings.Insolubles is syndiotactic polystyrene and Natene.Dsc analysis shows that the Tg of multipolymer is 91 ℃, and two melting peaks are respectively 260.4 ℃ and 131 ℃, proves that institute's synthetic multipolymer has the PE-b-sPS segmented copolymer of syndiotactic styrenic chain.
Claims (3)
1, a kind of catalyzer that is used to prepare syndiotactic polystyrene and polyethylene block multipolymer comprises organic metal titanium compound I and alkylaluminoxane II;
Cp is a cyclopentadienyl in the formula;
R
1Be furan group;
R
2For containing the alkyl of 1~4 carbon atom;
N is the oligomerisation degree of alkylaluminoxane, and its value is 6~40:
Aluminium is to the mol ratio 50~2000 of organo-metallic titanium compound I in the alkylaluminoxane II.
2, according to the described catalyzer that is used to prepare syndiotactic polystyrene and polyethylene block multipolymer of claim 1, it is characterized in that R
2Be methyl.
3, according to the described catalyzer that is used to prepare syndiotactic polystyrene and polyethylene block multipolymer of claim 1, the value that it is characterized in that oligomerisation degree n is 10~30.
Priority Applications (1)
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CN98110751A CN1065881C (en) | 1998-03-30 | 1998-03-30 | Catalyst for preparing block copolymer of syndiotactic polystyrene and polyethylene |
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CN98110751A CN1065881C (en) | 1998-03-30 | 1998-03-30 | Catalyst for preparing block copolymer of syndiotactic polystyrene and polyethylene |
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ID=5220774
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Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5100983A (en) * | 1990-03-07 | 1992-03-31 | Tosoh Corporation | Process for producing syndiotactic polymer of aromatic vinyl compounds |
US5652315A (en) * | 1992-06-04 | 1997-07-29 | Mitsui Toatsu Chemicals, Inc. | Method for preparing ethylene copolymer |
-
1998
- 1998-03-30 CN CN98110751A patent/CN1065881C/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5100983A (en) * | 1990-03-07 | 1992-03-31 | Tosoh Corporation | Process for producing syndiotactic polymer of aromatic vinyl compounds |
US5652315A (en) * | 1992-06-04 | 1997-07-29 | Mitsui Toatsu Chemicals, Inc. | Method for preparing ethylene copolymer |
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