CN1743348A - Catalyst component for olefinic polymerization and its catalyst - Google Patents
Catalyst component for olefinic polymerization and its catalyst Download PDFInfo
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- CN1743348A CN1743348A CN 200410073623 CN200410073623A CN1743348A CN 1743348 A CN1743348 A CN 1743348A CN 200410073623 CN200410073623 CN 200410073623 CN 200410073623 A CN200410073623 A CN 200410073623A CN 1743348 A CN1743348 A CN 1743348A
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- dibenzoate
- ester
- methyl
- catalyst component
- electron donor
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Abstract
This invention relates to a catalyst component for olefinic polymerization and its catalyst, said catalyst component comprises titanium compoumd with at least one Ti- halogen bond loaded on MgCl2nROH adduct and reaction product of two electronic doner compounds,wherein electronic doner compound A is chosen from poly alcohol ester compounds, and electronic doner compound B is chosen from ester,ether, ketone, amine and silicane compounds except compound A.The invented catalyst has high catalytic activity for olefinic polymerization ,in particular propylene polymerization, and wider molecular weight distribution.
Description
Technical field
The present invention relates to a kind of catalyst component and catalyzer of for olefines polymerization, and it is at alpha-olefin CH
2Application in the polyreaction of=CHR and composition thereof, wherein R is the alkyl of hydrogen or 1～12 carbon atom.More particularly, relate to a kind of catalyst component and catalyzer and application thereof that contains at least two kinds of electron donor compounds.
Technical background
Containing the titanium compound that is loaded on the magnesium halide in active and the catalyzer of electron donor compound is well known in the prior art.
U.S. Pat 4544717 discloses, and by add electron donor compound (being the internal electron donor compound) in the solid ingredient that contains titanium compound, can improve the stereospecificity of catalyzer.Up to now, existing many patent disclosures the multiple internal electron donor compound that is applicable to the preparation Ziegler-Natta catalyst, and the catalyzer that is used for olefinic polymerization that comprises these internal electron donor compounds.
These internal electron donor compounds mainly comprise: the electron donor compound of European patent EP 0045977 described phthalate, European patent EP 0361493, describe among the EP0728724 1, the 3-diether compound, describe among the Chinese patent CN1105671A 1, the 3-cyclohexadione compounds, Chinese patent CN1236732, CN1236733, CN1236734, the malonic ester compounds of the special replacement of describing among the CN1292800, the succinate compounds of describing in the PCT International Application No. WO 0063261, the beta substitution glutarate compounds of describing in the PCT International Application No. WO 0055215, the cyano group ester compound of describing among the Chinese patent CN1242780, the two amine electron donor compounds of describing among the Chinese patent CN1087918, the electron donor compound of the maleic acid ester class of describing in the PCT International Application No. WO 03022894, and Chinese patent CN1436766A, a kind of special polyol ester compounds of describing among the CN1436796A etc.
Owing to adopt different internal electron donor compounds to make prepared catalyzer have different characteristics, for example some catalyzer has higher activity, some catalyzer has better hydrogen regulation sensitivity, the polyolefin resin of some Preparation of Catalyst has wider molecular weight distribution or the like, but in polyolefinic industrial production, be starved of the employed catalyzer of polymerization and have very excellent comprehensive performances.In the prior art, people adopt the method that adds multiple internal electron donor compound in catalyst preparation process to improve the over-all properties of catalyzer usually.In disclosed patent WO9957160, WO0230998, WO03002617, JP2001139621, JP2002249507, KR20000026517 etc., set forth and used two or more internal electron donor compound to prepare catalyst component and the catalyzer that is used for olefinic polymerization simultaneously.But its result can't be satisfactory.。Usually, owing to after having used two or more internal electron donor compounds,, activity of such catalysts is decreased though molecular weight distribution that can resulting polymers broadens.
By repetition test, the inventor finds by selecting for use two kinds of internal electron donor compounds to use jointly at least, and wherein a kind of be polyol ester compound with special construction, can prepare the catalyst component and the catalyzer of high comprehensive performance.It is worthy of note that catalyzer of the present invention is being used for olefinic polymerization, is particularly showing very high activity and wider molecular weight distribution during propylene polymerization.
Summary of the invention
The invention provides a kind of catalyst component that is used for olefinic polymerization, this catalyst component comprises titanium, magnesium, halogen and at least two kinds of electron donor compd As and B, and wherein the electron donor compd A is selected from the polyol ester compounds shown in general formula (I):
R in the formula
1-R
6, R
1-R
2nGroup is hydrogen, halogen or the replacement identical or inequality or the C of unsubstituted straight or branched
1-C
20Alkyl, C
3-C
20Cycloalkyl, C
6-C
20Aryl, C
7-C
20Alkaryl, C
7-C
20Aralkyl, C
2-C
10Alkylene, C
10-C
20Fused ring aryl or C
2-C
10Ester group; But R
1And R
2Not hydrogen, R
3-R
6And R
1-R
2nComprise one or several heteroatoms on the group arbitrarily as carbon or hydrogen atom or both substituents, described heteroatoms is selected from nitrogen, oxygen, sulphur, silicon, phosphorus or halogen atom, R
3-R
6And R
1-R
2nOne or more in the group can link up into ring; N is the integer of 0-10;
The electron donor compd B is selected from ester, ether, ketone, amine and the silane compound except that compd A.
This class polyol ester compounds is disclosed among Chinese patent CN1436766A, CN1436796A and the CN1453298A, and its associated viscera is introduced the present invention as a reference.
In above-mentioned polyol ester compounds, the compound shown in the preferred formula (II).
R wherein
1-R
6, R
1-R
2Definition in group such as the general formula (I).
In the polyol ester compounds shown in general formula (I) or the general formula (II), preferred R
3, R
4, R
5, R
6Be not hydrogen simultaneously, and R
3, R
4, R
5And R
6In have at least a group to be selected from halogen, C
1-C
10The alkyl of straight or branched, C
3-C
10Cycloalkyl, C
6-C
10Aryl, C
7-C
10Alkaryl or aralkyl.
In addition, general formula (I) also comprises the compound shown in the general formula (III), wherein R
1-R
2Definition in group such as the general formula (I); R ' is the C of hydrogen identical or inequality, halogen atom, straight or branched
1-C
20Alkyl, C
3-C
20Cycloalkyl, C
6-C
20Aryl, C
7-C
20Alkaryl or C
7-C
20Aralkyl.
Above-mentioned general formula (I), (II) and (III) shown in the polyol ester compounds in, R
1And R
2In have at least one to be selected from phenyl, halogenated phenyl, alkyl phenyl or halogenated alkyl phenyl.
Electron donor compd A described in the catalyst component of the present invention specifically can adopt:
1,2 - propylene glycol benzoate, 1,2 - propanediol bis (p-chlorobenzoic acid) ester, 1,2 - propanediol bis
(M-chloroperbenzoic acid) ester, 1,2 - propanediol bis (p-bromo-benzoic acid) ester, 1,2 - propanediol bis (o-bromophenyl
Formic acid) ester, 1,2 - propanediol bis (p-toluic acid) ester, 1,2 - propanediol bis (p-tert-butyl-benzoic
Acid) ester, 1,2 - propanediol bis (p-butyl benzoic acid) ester, 1,2 - propanediol, cinnamic acid esters, 1,2 -
Propylene glycol cinnamate 2 - methyl-1,2 - propanediol dibenzoate 2 - methyl-1 ,2 - propanediol bis (p-
Chlorobenzoic acid) ester of 2 - methyl-1,2 - propanediol bis (m-chloroperbenzoic acid) ester of 2 - methyl-1,2 - propanediol bis
(P-bromo benzoic acid) ester of 2 - methyl -1,2 - propanediol bis (o-bromo-benzoic acid) ester of 2 - methyl-1 ,2 - malonyl
Glycol di (p-methylbenzoate) ester of 2 - methyl-1,2 - propanediol bis (p-tert-butylbenzoic acid) ester of 2 -
Methyl-1 ,2 - propanediol bis (p-butyl benzoic acid) ester of 2 - methyl-1,2 - propanediol, cinnamic acid esters,
2 - methyl-1 ,2 - cinnamate glycol, 1,3 - propylene glycol dibenzoate 2 - methyl-1,3 - propanediol bis
Benzoate 2 - ethyl-1 ,3 - propanediol dibenzoate 2 - propyl-1 ,3 - propanediol dibenzoate 2 -
Butyl-1 ,3 - propanediol dibenzoate, 2,2 - dimethyl-1 ,3 - propanediol dibenzoate, (R) -1 - phenyl
-1,3 - Propanediol dibenzoate, (S) -1 - phenyl-1 ,3 - propanediol dibenzoate, 1,3 - diphenyl-1 ,3 -
Propylene glycol dibenzoate, 1,3 - diphenyl-2 - methyl-1,3 - propanediol dibenzoate, 1,3 - diphenyl-
1,3 - propylene glycol n-propyl ester, 1,3 - diphenyl-2 - methyl-1,3 - propanediol dipropionate, 1,3 - diphenyl-
-2 - Methyl-1,3 - propanediol diacetate, 1,3 - diphenyl-2 ,2 - dimethyl-1 ,3 - propanediol dibenzoate,
1,3 - diphenyl-2 ,2 - dimethyl-1 ,3 - propanediol dipropionate, 1,3 - di-tert-butyl-2 - ethyl-1 ,3 - propanediol
Dibenzoate, 1,3 - diphenyl-1 ,3 - propanediol diacetate 2 - ethyl-2 - butyl-1 ,3 - propanediol diphenyl
Methyl ester, 2,2 - diethyl-1 ,3 - propanediol dibenzoate, 2,2 - dimethoxy-1 ,3 - propanediol bis
Benzoate, 2 - methyl -2 - propyl-1 ,3 - propanediol dibenzoate 2 - isopropyl-2 - isopentyl-1 ,3 - C
Glycol dibenzoate 2 - isopropyl-2 - isopentyl-1 ,3 - propylene glycol esters of p-chlorobenzoic acid 2 - isopropyl-2 -
Isopentyl-1 ,3 - chloroperbenzoic acid glycol ester of 2 - isopropyl-2 - isopentyl-1 ,3 - propanediol bis (p-methyl
Benzoic acid) ester of 2 - isopropyl-2 - isopentyl-1 ,3 - propanediol bis (p-benzoic acid) ester of 2 -
Isopropyl-2 - isopentyl-1 ,3 - propylene glycol monopropyl ester Benzoic acid 2 - isopropyl-2 - isopentyl-1 ,3 - malonic
Dipropionate alcohol 2 - isopropyl-2 - isopentyl-1 ,3 - propanediol diacrylate 2 - isopropyl-2 - isopentyl
1,3 - propylene glycol cinnamate, 2,2 - diisobutyl-1 ,3 - propanediol dibenzoate 2 - isopropyl-2 -
Isopentyl-1 ,3 - propanediol, 2,2 '- biphenyl - dimethyl ester 2 - isopropyl-2 - isopentyl-1 ,3 - propanediol - o-phenylenediamine
Acid esters, 1,3 - diisopropyl-1 ,3 - propanol bis (4 - butyl benzoic acid) ester, 2 - methyl -2 - ethyl-1 ,3 -
Dipropylene glycol methyl ester, 1 - phenyl - 2 - amino-1 ,3 glycol benzoate, 2,2 - dimethyl-1 ,3 -
Propylene glycol dibenzoate, 1,2 - butylene glycol dibenzoate 2 - methyl-1,2 - butylene glycol dibenzoate,
2,3 - dimethyl-1 ,2 - butylene glycol dibenzoate, 2,3 - dimethyl-1 ,2 - butylene glycol esters of p-chlorobenzoic acid,
2,3,3 - trimethyl 1,2 - butylene glycol dibenzoate, 2,3,3 - trimethyl 1,2 - butanediol di chloro
Benzoate, 1,2 - butylene glycol esters of p-chlorobenzoic acid, 2,3 - butylene glycol dibenzoate, 2,3 - butanediol
Di-o-bromo-benzoate, 2,3 - butanediol dimethacrylate benzoate, 2,3 - butylene glycol ester of m-chloroperbenzoic acid,
2 - methyl-2,3 - butylene glycol dibenzoate 2 - methyl-2,3 - butanediol di-o-bromo-benzoate 2 - methyl-
2,3 - butanediol dimethacrylate benzoate 2 - methyl-2 - chlorobenzoic acid ester of butylene glycol, 2,3 - dimethyl
-2,3 - Butylene glycol dibenzoate, 2,3 - dimethyl-2,3 - butanediol di-o-bromo-benzoate, 2,3 -
Dimethyl -2,3 - dimethyl benzoate butanediol, 2,3 - dimethyl-2 ,3 - chloroperbenzoic acid butylene glycol ester,
1 - phenyl - 2 - methyl-1,3 - butylene glycol benzoate, phenyl-2 - methyl-1,3 - butanediol bis pivalate,
1 - furan-2 - methyl-1,3 - butylene glycol dibenzoate, 1,4 - butylene glycol dibenzoate, 2,3 - diisopropyl
Yl 1,4 - butylene glycol dibenzoate, 2,3 - dimethyl -1,4 - butylene glycol dibenzoate, 2,3 -
Ethyl 1,4 - butylene glycol dibenzoate, 2,3 - dibutyl-1 ,4 - butylene glycol dibenzoate, 2,3 -
Diisopropyl 1,4 - butylene glycol butyrate, 4,4,4 - trifluoro-1 - (2 - naphthyl) - 1,3-butanediol Diphenyl
Methyl ester, 2,3 - pentanediol dibenzoate 2 - methyl-2 ,3 - pentanediol dibenzoate 3 - methyl-2 -
Pentanediol dibenzoate ester, 4 - methyl-2,3 - pentanediol dibenzoate, 2,3 - dimethyl-2 - pentyl glycol
Benzoate, 2,4 - dimethyl-2 ,3 - pentanediol dibenzoate, 3,4 - dimethyl-2 ,3 - pentanediol benzophenone
Ester, 4,4 - dimethyl-2 ,3 - pentanediol dibenzoate, 2,3,4 - trimethyl-2,3 - pentanediol benzophenone
Ester, 2,4,4 - trimethyl-2,3 - pentanediol dibenzoate, 3,4,4 - trimethyl-2,3 - pentanediol
Dibenzoate, 2,3,4,4 - tetramethyl-2,3 - pentanediol dibenzoate 3 - ethyl-2,3 - pentanediol
Dibenzoate 2 - Synthesis of methyl 3 - ethyl 2,3 - pentanediol dibenzoate 2 - Synthesis of methyl 3 - ethyl-4 - methyl-2 -
Pentanediol dibenzoate 2 - Synthesis of methyl 3 - ethyl 4,4 - dimethyl-2,3 - pentanediol dibenzoate, 2,4 -
Pentanediol dibenzoate 3 - methyl-2 ,4 - pentanediol dibenzoate 3 - ethyl-2 ,4 - pentanediol benzophenone
Ester 3 - propyl-2,4 - pentanediol dibenzoate 3 - butyl 2,4 - pentanediol dibenzoate, 3,3 -
Dimethyl 2,4 - pentanediol dibenzoate, (2S, 4S) - (+) -2,4 - pentanediol dibenzoate, (2R,
4R) - (+) -2,4 - pentanediol dibenzoate, 2,4 - pentanediol di (p-chlorobenzoic acid) ester, 2,4 - E
Glycol di (m-chloroperbenzoic acid) ester, 2,4 - pentanediol di (p-bromo-benzoic acid) ester, 2,4 - pentanediol di (o-
Bromo acid) ester, 2,4 - pentanediol di (p-methylbenzoate) acrylate, 2,4 - pentanediol di (p-tert-butyl
Acid) ester, 2,4 - pentanediol di (p-butyl benzoic acid) ester, 2,4 - pentanediol, cinnamic acid esters,
2,4 -, 1,3-pentyl glycol cinnamate - pentanediol dipropionate 2 - methyl-1,3 - pentanediol dibenzoate,
2 - methyl-1,3 - pentanediol di (p-chlorobenzoic acid) ester of 2 - methyl-1,3 - pentanediol di (p-methylbenzoate)
Esters of 2 - butyl-1 ,3 - pentanediol di (p-methylbenzoate) ester 2 - methyl-1,3 - pentanediol di (p-tert-butyl
-Benzoic acid) ester of 2 - methyl-1,3 - pentanediol, neopentyl ester 2 - methyl-1,3 - pentanediol benzoic acid
Ester, 2,2 - dimethyl-1 ,3 - pentanediol dibenzoate, 2,2 - dimethyl-1 ,3 - pentanediol, cinnamic acid
Ester 2 - ethyl-1 ,3 - pentanediol dibenzoate 2 - butyl-1 ,3 - pentanediol dibenzoate 2 - allyl
Yl 1,3 - pentanediol dibenzoate 2 - methyl-1 ,3 - pentanediol, cinnamic acid ester 2 - methyl-1 ,3 -
Pentanediol dibenzoate 2 - ethyl-1 ,3 - pentanediol dibenzoate 2 - propyl-1 ,3 - neopentyl glycol
Benzoate 2 - butyl-1 ,3 - pentanediol dibenzoate, 2,2 - dimethyl-1 ,3 - pentanediol benzophenone
Ester, 1,3 - pentanediol di (p-chlorobenzoic acid) ester, 1,3 - pentanediol di (m-chloroperbenzoic acid) ester, 1,3 -
Neopentyl glycol di (p-bromo-benzoic acid) ester, 1,3 - pentanediol di (o-bromo-benzoic acid) ester, 1,3 - neopentyl glycol
(P-toluic acid) ester, 1,3 - pentanediol di (p-tert-butylbenzoic acid) ester, 1,3 - pentanediol di (p-
Butyl benzoic acid) ester, 1,3 - pentanediol, cinnamic acid esters, 1,3 - neopentyl glycol cinnamate, 1,3 -
Pentanediol dipropionate 2 - methyl-1,3 - pentanediol dibenzoate 2 - methyl-1,3 - pentanediol di (p-chloro
Acid) ester of 2 - methyl-1,3 - pentanediol di (p-methylbenzoate) ester 2 - butyl-1 ,3 - pentyl glycol
(P-toluic acid) ester of 2 - methyl-1,3 - pentanediol di (p-tert-butylbenzoic acid) ester of 2 - methyl-1 ,3 -
Pentanediol, neopentyl ester 2 - methyl-1,3 - pentanediol, cinnamic acid esters, 2,2 - dimethyl-1 ,3 - glutaryl
Alcohol dibenzoate, 2,2 - dimethyl-1 ,3 - pentanediol, cinnamic acid ester 2 - ethyl-1 ,3 - pentanediol
Dibenzoate 2 - butyl-1 ,3 - pentanediol dibenzoate 2 - allyl 1,3 - pentanediol dibenzoate,
2 - methyl-1,3 - pentanediol, cinnamic acid ester, 2,2,4 - trimethyl-1 ,3 - pentanediol dibenzoate,
2,2,4 - trimethyl-1 ,3 - pentanediol, diisopropyl ester, 1 - trifluoromethyl-3 - methyl-2 ,4 - neopentyl glycol
Benzoate, 2,4 - pentanediol two pairs fluoromethyl benzoate, 2,4 - pentanediol di (2 - furoic acid)
Esters of 3 - methyl - 3 - butyl 2,4 - pentanediol dibenzoate, 2,2 - dimethyl-1,5 - pentanediol dibenzoate,
1,5 - diphenyl-1,5 - pentanediol dibenzoate, 1,5 - diphenyl-1,5 - pentanediol dipropionate, 2,3 - hexyl
Glycol dibenzoate 2 - methyl-2 ,3 - hexanediol dibenzoate 3 - methyl 2,3 - hexanediol dibenzoate
Ester, 4 - methyl 2,3 - hexanediol dibenzoate, 5 - methyl-2 ,3 - hexanediol dibenzoate, 2,3 - dimethyl
-2,3 - Hexanediol dibenzoate, 2,4 - dimethyl-2 ,3 - hexanediol dibenzoate, 2,5 - dimethyl-
2,3 - hexanediol dibenzoate, 3,4 - dimethyl-2 ,3 - hexanediol dibenzoate, 3,5 - dimethyl -2,3 -
Hexanediol dibenzoate, 4,4 - dimethyl-2 ,3 - hexanediol dibenzoate, 4,5 - dimethyl-2 ,3 - hexanediol
Alcohol dibenzoate, 5,5 - dimethyl-2 ,3 - hexanediol dibenzoate, 2,3,4 - trimethyl-2 ,3 - hexanediol
Alcohol dibenzoate, 2,3,5 - trimethyl 2,3 - hexanediol dibenzoate, 2,4,4 - trimethyl-2 ,3 -
Hexanediol dibenzoate, 2,4,5 - trimethyl 2,3 - hexanediol dibenzoate, 2,5,5 - trimethyl-
2,3 - hexanediol dibenzoate, 3,4,4 - trimethyl 2,3 - hexanediol dibenzoate, 3,4,5 -
Trimethyl-2,3 - hexanediol dibenzoate, 3,5,5 - trimethyl 2,3 - hexanediol dibenzoate, 2,
3,4,4 - tetramethyl-2,3 - hexanediol dibenzoate, 2,3,4,5 - tetramethyl-2,3 - diphenyl-hexanediol
Ester, 2,3,5,5 - tetramethyl-2,3 - hexanediol dibenzoate 3 - ethyl-2 ,3 - hexanediol diphenyl
Methyl ester 3 - propyl 2,3 - hexanediol dibenzoate 3 - isopropyl-2 ,3 - hexanediol dibenzoate ester, 4 -
Ethyl-2 ,3 - hexanediol dibenzoate, 2 - methyl -3 - ethyl-2 ,3 - hexanediol dibenzoate, 2 - methyl -4 -
Ethyl-2 ,3 - hexanediol dibenzoate 2 - methyl - 3 - propyl-2 ,3 - hexanediol dibenzoate 3 - methyl - 4 -
Ethyl-2 ,3 - hexanediol dibenzoate, 3,4 - diethyl 2,3 - hexanediol dibenzoate 3 - propyl-4 -
Ethyl-2 ,3 - hexanediol dibenzoate, 2,4 - dimethyl-3 - ethyl-2 ,3 - hexanediol dibenzoate, 2,
5 - dimethyl-3 - ethyl-2 ,3 - hexanediol dibenzoate, 2,4,4 - trimethyl-3 - ethyl-2 ,3 - hexanediol
Dibenzoate, 2,4,5 - trimethyl-3 - ethyl-2 ,3 - hexanediol dibenzoate, 2,4 - dimethyl-3 -
Ethyl-2 ,3 - hexanediol dibenzoate, 2,5 - dimethyl-3 - propyl-2 ,3 - hexanediol dibenzoate, 2,
4,4 - trimethyl-3 - propyl-2 ,3 - hexanediol dibenzoate, 2,5,5 - trimethyl-3 - propyl-2 ,3 - hexanediol
Alcohol dibenzoate, 2,4,5 - trimethyl-3 - propyl-2 ,3 - hexanediol dibenzoate, 2 - methyl -3,
4 - diethyl 2,3 - hexanediol dibenzoate 2 - ethyl-1 ,3 - hexanediol dibenzoate 2 - propyl-1 ,3 -
Hexanediol dibenzoate 2 - butyl-1 ,3 - hexanediol dibenzoate ester, 4 - ethyl-1,3 - hexanediol benzophenone
Ester 4 - methyl 1,3 - hexanediol dibenzoate 3 - methyl 1,3 - hexanediol dibenzoate 3 - ethyl-
1,3 - hexanediol dibenzoate, 2,2,4,6,6 - pentamethyl-3 ,5 - dibenzoate hexanediol, 2,5 - hexanediol
Dibenzoate, 2,5 - dimethyl-2 ,5 - dibenzoate hexanediol, 2,5 - dimethyl 2,5 - hexanediol, dipropylene
Ester, 2,5 - dimethyl-3 - yne 2,5 - hexanediol dibenzoate 3 - alkyne 2,5 - hexanediol dibenzoate
(T), 3 - alkyne 2,5 - hexanediol dibenzoate (S), 3 - alkyne 2,5 - hexanediol di (2 - furoic acid) ester, 3,4 -
Dibutyl 1,6 - hexanediol dibenzoate, 1,6 - hexanediol dibenzoate, 6 - heptene 2,4 - heptane diol
Dibenzoate 2 - methyl-6 - heptene 2,4 - heptane diol dibenzoate 3 - methyl-6 - heptene-2, 4 -
Heptane diol dibenzoate ester, 4 - methyl-6 - heptene 2,4 - heptane diol dibenzoate, 5 - methyl-6 - hept-ene-2,
4 - heptane diol dibenzoate, 6 - methyl-6 - heptene 2,4 - heptane diol dibenzoate 3 - ethyl-6 - heptene
2,4 - heptane diol dibenzoate ester, 4 - ethyl-6 - heptene 2,4 - heptane diol dibenzoate, 5 - ethyl-6 -
Heptene 2,4 - heptane diol dibenzoate, 6 - ethyl-6 - heptene 2,4 - heptane diol dibenzoate 3 - C
-6 - heptene 2,4 - heptane diol dibenzoate ester, 4 - propyl-6 - heptene 2,4 - heptane diol dibenzoate,
5 - propyl-6 - heptene 2,4 - heptane diol dibenzoate, 6 - propyl-6 - heptene 2,4 - heptane diol dibenzoate
Ester 3 - butyl-6 - heptene 2,4 - heptane diol dibenzoate ester, 4 - butyl-6 - heptene 2,4 - diphenyl heptanediol
Methyl ester, 5 - butyl-6 - heptene 2,4 - heptane diol dibenzoate, 6 - butyl-6 - heptene 2,4 - heptane diol
Dibenzoate, 3,5 - dimethyl-6 - heptene 2,4 - heptane diol dibenzoate, 3,5 - diethyl-6 -
Heptene 2,4 - heptane diol dibenzoate, 3,5 - propyl-6 - heptene 2,4 - heptane diol dibenzoate,
3,5 - butyl-6 - heptene 2,4 - heptane diol dibenzoate, 3,3 - dimethyl-6 - heptene-2 ,4 - heptadienoic
Alcohol dibenzoate, 3,3 - diethyl-6 - heptene 2,4 - heptane diol dibenzoate, 3,3 - propyl-6 -
Heptene 2,4 - heptane diol dibenzoate, 3,3 - butyl-6 - heptene 2,4 - heptane diol dibenzoate,
3,5 - heptanediol dibenzoate 2 - methyl-3 ,5 - heptane diol dibenzoate 3 - methyl-3 ,5 - heptane diol
Benzoic acid ester, 4 - methyl-3 ,5 - heptane diol dibenzoate, 5 - methyl-3 ,5 - heptane diol dibenzoate, 6 -
Methyl-3 ,5 - heptane diol dibenzoate 3 - ethyl-3 ,5 - heptane diol dibenzoate ester, 4 - ethyl-3 ,5 - pimelic
Alcohol dibenzoate, 5 - ethyl-3 ,5 - heptane diol dibenzoate 3 - propyl 3,5 - heptane diol dibenzoate,
4 - propyl 3,5 - heptane diol dibenzoate 3 - butyl 3,5 - heptane diol dibenzoate, 2,3 - dimethyl-
3,5 - heptane diol dibenzoate, 2,4 - dimethyl-3 ,5 - heptane diol dibenzoate, 2,5 - dimethyl-3 ,5 -
Heptane diol dibenzoate, 2,6 - dimethyl-3 ,5 - heptane diol dibenzoate, 3,3 - dimethyl-3 ,5 - heptanedionate
Alcohol dibenzoate, 4,4 - dimethyl-3 ,5 - heptane diol dibenzoate, 6,6 - dimethyl-3 ,5 - heptanediol
Dibenzoate, 2,6 - dimethyl-3 ,5 - heptane diol dibenzoate, 3,4 - dimethyl-3 ,5 - heptane diol
Benzoate, 3,5 - dimethyl-3 ,5 - heptane diol dibenzoate, 3,6 - dimethyl -3,5 - diphenyl heptanediol
Methyl ester, 4,5 - dimethyl-3 ,5 - heptane diol dibenzoate, 4,6 - dimethyl-3 ,5 - heptanediol benzophenone
Ester, 4,4 - dimethyl-3 ,5 - heptane diol dibenzoate, 6,6 - dimethyl-3 ,5 - heptane diol dibenzoate
Ester, 2 - methyl -3 - ethyl-3 ,5 - heptane diol dibenzoate, 2 - methyl -4 - ethyl-3 ,5 - heptanediol benzophenone
Ester, 2 - methyl -5 - ethyl-3 ,5 - heptane diol dibenzoate 3 - methyl - 3 - ethyl 3,5 - diphenyl heptanediol
Methyl ester 3 - methyl - 4 - ethyl-3,5 - heptane diol dibenzoate 3 - methyl-5 - ethyl-3 ,5 - heptane diol
Benzoic acid ester, 4 - methyl-3 - ethyl-3 ,5 - heptane diol dibenzoate ester, 4 - methyl - 4 - ethyl-3 ,5 - heptanediol
Dibenzoate ester, 4 - methyl-5 - ethyl-3 ,5 - heptane diol dibenzoate, 2 - methyl -3 - propyl-3 ,5 - pimelic
Alcohol dibenzoate 2 - methyl - 4 - propyl 3,5 - heptane diol dibenzoate, 2 - methyl -5 - propyl-3, 5 - G
Diol dibenzoate 3 - methyl - 3 - propyl-3,5 - heptane diol dibenzoate 3 - methyl - 4 - propyl-3, 5 -
Heptane diol dibenzoate 3 - methyl-5 - propyl 3,5 - heptane diol dibenzoate ester, 4 - methyl - 3 - propyl-3, 5 -
Heptane diol dibenzoate ester, 4 - methyl - 4 - propyl 3,5 - heptane diol dibenzoate ester, 4 - methyl-5 - propyl-3, 5 -
Heptane diol dibenzoate, 6 - methyl-2 ,4 - heptane diol di (p-chlorobenzoic acid) ester, 6 - methyl-2 ,4 - heptanediol
Bis (p-toluic acid) ester, 6 - methyl-2 ,4 - heptane diol di (meth acid) ester, 6 - methyl-2 ,4 - G
Neopentyl glycol ester, 6 - heptene 2,4 - heptane neopentyl glycol ester, 3,6 - dimethyl-2,4 - diphenyl heptanediol
Ester, 2,2,6,6 - tetramethyl-3 ,5 - heptane diol dibenzoate, 2,6 - dimethyl-2,6 - diphenyl heptanediol
Methyl ester 4 - methyl-3,5 - octanediol dibenzoate ester, 4 - ethyl-3,5 - octanediol dibenzoate
4 - propyl 3,5 - octanediol dibenzoate, 5 - propyl 3,5 - octanediol dibenzoate ester, 4 - butyl - 3,
5 - dibenzoate octanediol, 4,4 - dimethyl-3 ,5 - dibenzoate octanediol, 4,4 - Diethyl-3,
5 - dibenzoate octanediol, 4,4 - dipropyl-3 ,5 - octanediol dibenzoate ester, 4 - methyl - 4 - ethyl-3,
5 - octanediol dibenzoate 3 - phenyl-3 ,5 - dibenzoate octanediol, 2 - methyl -3 - ethyl-3 ,5 -
Octylene glycol dibenzoate, 2 - methyl -4 - ethyl 3,5 - octanediol dibenzoate, 2 - methyl -5 - ethyl-3,
5 - octanediol dibenzoate 2 - methyl-6 - ethyl-3 ,5 - dibenzoate octanediol, 5 - methyl-4 ,6-nonyl
Glycol dibenzoate, 5 - ethyl-4 ,6 nonane diol dibenzoate, 5 - propyl-4 ,6 nonane diol dibenzoate
Ester, 5 - butyl-4 ,6 nonane diol dibenzoate, 5,5 - dimethyl -4,6 nonane diol dibenzoate, 5,
5 - diethyl glycol dibenzoate 4,6 nonane, 5,5 - dipropyl-4 ,6 nonane diol dibenzoate, 5,5 -
Dibutyl glycol dibenzoate -4,6 nonane, 5 - methyl - 4 - ethyl-4 ,6 nonane diol dibenzoate, 5 - phenyl-
-4,6 Nonane diol dibenzoate, 4,6 - nonane diol dibenzoate, 1,1 - cyclohexane diol dibenzoate,
1,2 - cyclohexane diol dibenzoate, 1,3 - cyclohexane diol dibenzoate, 1,4 - cyclohexane diol
Benzoate, 1,1 - dibenzoyl ethyl cyclohexane, 1,4 - benzoyloxymethyl-cyclohexane, 1,1 -
Benzoyloxy-methyl-3 - cyclohexene, 1,1 - dipropyl acyloxy-3 - cyclohexene, 9,9 - bis (phenylmethoxy carboxymethyl)
Fluorene, 9,9 - double ((carboxy-methoxy benzoyl) methyl) fluorene, 9,9 - double ((m-chlorophenyl A carboxy) A
Yl) fluorene, 9,9 - bis ((carboxy methyl p-chlorophenyl) methyl) fluorene, 9,9 - bis (carboxymethyl cinnamon) fluorene,
9 - (carboxy-methyl-benzyl) -9 - (prop-carboxy methyl) fluorene, 9,9 - bis (carboxymethyl c) fluorene, 9,9 - bis
(Acrylic carboxymethyl)-fluorene, 9,9 - bis (neopentyl carboxymethyl)-fluorene, 9,9 - diphenyl fluorene dimethanol
Ester, 1,2 - dihydroxybenzene dibenzoate, 1,3 - dihydroxybenzene dibenzoate, 1,4 - dihydroxybenzene dibenzoate
Ester, 2,2 '- linking two phenol dibenzoate, 2,2' - methylene-bridged binaphthol dibenzoate, 1,2 -
Benzene dimethanol dibenzoate, 1,3 - benzene dimethanol dibenzoate, 1,4 - benzene dimethanol dibenzoate,
2,2 '- biphenyl pivalate dimethanol, 2,2' - biphenyl-dimethanol dibenzoate, 2,2 '- biphenyl
Methanol dipropionate, 2,2 '- binaphthyl dimethanol dibenzoate, 2,5 - hexane carboxy cinnamon, four benzoic
Carboxyl methane, 1,2,3 - trityl carboxyl propane.
...
Other at least a electron donor compd B can be selected from ester, ether, ketone, amine and the silane compound etc. except that compd A in the catalyst component of the present invention.Preferred monobasic or polyhydric aliphatic family carboxylicesters or aromatic carboxylic acid esters and diether compound.
Wherein monobasic or polyhydric aliphatic family carboxylicesters or aromatic carboxylic acid esters are as benzoates, phthalate, malonic ester class, succinate class, glutarate class, pivalate or carbonates etc.Concrete as: ethyl benzoate, diethyl phthalate, diisobutyl phthalate, n-butyl phthalate, dimixo-octyl phthalate, dinoctyl phthalate, diethyl malonate, butyl ethyl malonate, 2,3-di-isopropyl ethyl succinate, 2,3-di-isopropyl di-iso-octyl succinate, 2,3-di-isopropyl dibutyl succinate, 2,3-di-isopropyl succsinic acid dimethyl esters, 2,2-dimethyl succinate diisobutyl ester, 2-ethyl-2-methylsuccinic acid diisobutyl ester, 2-ethyl-2-methylsuccinic acid diethyl ester, diethylene adipate, Polycizer W 260, ethyl sebacate, Uniflex DBS, diethyl maleate, maleic acid n-butyl, the naphthalene dicarboxylic acids diethyl ester, the naphthalene dicarboxylic acids dibutylester, triethyl trimellitate, tributyl trimellitate, the benzene-1,2,3-tricarboxylic acid triethyl, the benzene-1,2,3-tricarboxylic acid tri-n-butyl, the pyromellitic acid tetra-ethyl ester, pyromellitic acid four butyl esters etc.
1 shown in the diether compound preferred formula (IV) wherein, 3-two ethers, wherein R
I, R
II, R
III, R
IV, R
VAnd R
VIMutually the same or inequality, be selected from the C of hydrogen, halogen atom, straight or branched
1-C
20Alkyl, C
3-C
20Cycloalkyl, C
6-C
20Aryl, C
7-C
20Alkaryl, C
7-C
20A kind of in the aralkyl, and R
VIIAnd R
VIIICan be identical or different, be selected from the C of straight or branched
1-C
20Alkyl, C
3-C
20Cycloalkyl, C
6-C
20Aryl, C
7-C
20Alkaryl, C
7-C
20A kind of in the aralkyl; R
I-R
VIGroup between can be keyed to ring.Preferred R wherein
VIIAnd R
VIIIBe selected from C
1-C
41 of alkyl, the 3-diether.
These 1, the 3-diether compounds is disclosed among Chinese patent ZL89108368.5 and the Chinese patent CN11411285A, its associated viscera is introduced the present invention as a reference.
As above said, except above-mentioned electron donor compd A and B, catalyst component of the present invention also comprises titanium, magnesium and halogen.Particularly preferably, this catalyst component is that load has the titanium compound with at least one Ti-halogen bond and the reaction product of above-mentioned electron donor compound on a kind of halogenide of magnesium, the halogenide of described magnesium preferably has the magnesium dihalide of active state, is more preferably magnesium dichloride.This magnesium dichloride is well-known as the carrier of Ziegler-Natta catalyst in the art.Usually, this magnesium dichloride with active state is characterised in that, in X ray diffracting spectrum, the intensity that appears at the intensive diffraction peak in the diffracting spectrum of nonactive magnesium dichloride reduce and be expanded into one dizzy.
Usual method is at a kind of MgCl
2.nROH load has titanium compound and the reaction product of described two kinds of electron donor compd As and B, the wherein MgCl with at least one Ti-halogen bond on the adducts
2.nROH adducts is magnesium dichloride and pure adducts, preferred particle spherical in shape, and wherein n is generally 1.5～4, and preferred 2.0～3.5; R is the alkyl of carbon number 1-4, described alcohol such as ethanol, propyl alcohol, Virahol, butanols, isopropylcarbinol, isooctyl alcohol etc.
Described general formula with titanium compound of at least one Ti-halogen bond is: TiX
n(OR)
4-n, R is C in the formula
1～C
20Alkyl, be preferably normal-butyl/isobutyl-, 2-ethylhexyl, n-octyl and phenyl; X is a halogen, and n is 1～4.Concrete titanium compound can be selected titanium tetrahalide, particularly titanium tetrachloride for use; Three chlorocarbon oxygen machine base titanium, particularly trichlorine butoxy and Trichlorophenoxy titaniums; Four titan-alkoxides, particularly four titanium butoxide, purity titanium tetraethoxide.
With above-mentioned MgCl
2.nROH adducts particle and multiple electron donor compound of the present invention and titanium compound react, and finally obtain catalyst component of the present invention.Relevant preparation process can be carried out with reference to disclosed method among Chinese patent CN1036011C, the CN1330086A, and disclosed associated viscera is incorporated herein the present invention as a reference.
In the preparation of catalyst component, with respect to MgCl
2, common mole with 0.001 to 0.5, preferred 0.001 to 0.1 recently uses compd A; Mole with 0.01 to 5, preferred 0.05 to 1 recently uses the electron donor compd B.
Compd A and electron donor compd B can use in many ways jointly, and preferably the two uses in different steps, under the different condition.With regard to usage quantity, the mol ratio of compd A and compd B is generally 0.01～0.5, and preferred 0.05～0.15.
Ingredient of solid catalyst of the present invention changes into the catalyzer that is used for olefinic polymerization by reacting according to currently known methods and organo-aluminium compound.
In particular, the purpose of this invention is to provide a kind of alpha-olefin CH that is used for
2=CHR polymeric catalyzer, wherein R is the alkyl of hydrogen or 1～12 carbon atom, this catalyzer comprises the reaction product between following material:
(1), a kind of above-mentioned ingredient of solid catalyst that contains Mg, Ti and halogen and electron donor compound;
(2), a kind of alkylaluminium cpd, and randomly,
(3), one or more electron donor compounds (external electron donor).
The alkylaluminium cpd preferred formula is AlR
nX
3-nCompound, R is the alkyl of hydrogen or carbonatoms 1～20, particularly alkyl, aralkyl, aryl etc. in the formula; X is halogen, particularly chlorine and bromine; N is the number of 0＜n≤3.Alkylaluminium cpd of the present invention comprises: trialkylaluminiums such as trimethyl aluminium, triethyl aluminum, triisobutyl aluminium, trioctylaluminum; Alkyl aluminium hydrides such as one hydrogen diethyl aluminum, a hydrogen diisobutyl aluminum; Aluminium diethyl monochloride, a chloro-di-isobutyl aluminum, sesquialter ethyl aluminum chloride, aluminum alkyls muriates such as ethyl aluminum dichloride wherein are preferably triethyl aluminum and triisobutyl aluminium.
The consumption of aluminum alkyls is: wherein the mol ratio of titanium is 5-5000 in aluminium and the solid constituent (1), is preferably 20-500.
The external electron donor compound is preferably silicoorganic compound.Its general formula is RnSi (OR ')
4-n, 0＜n in the formula≤3, R and R ' they are alkyl of the same race or not of the same race, cycloalkyl, aryl, haloalkyl etc. in the general formula, R also can be halogen or hydrogen atom.Silicoorganic compound of the present invention comprise the trimethylammonium methoxy silane, trimethylethoxysilane, trimethyl phenoxysilane, dimethyldimethoxysil,ne, dimethyldiethoxysilane, methyl-t-butyldimethoxysilane, two phenoxy group dimethoxy silane, the phenylbenzene diethoxy silane, phenyltrimethoxysila,e, phenyl triethoxysilane, vinyltrimethoxy silane, cyclohexyl methyl dimethoxy silane, dicyclopentyl dimethoxyl silane, 2-ethyl piperidine base-2-tertiary butyl dimethoxy silane, (1,1,1-three fluoro-2-propyl group)-2-ethyl piperidine base dimethoxy silane and (1,1,1-three fluoro-2-propyl group)-methyl dimethoxysilane etc.
In addition, the external electron donor of catalyzer of the present invention also can select for use Chinese patent CN1020448C and CN1141285A disclosed 1,3-diether, and the disclosed succinate of Chinese patent CN1313869A.
The consumption of external electron donor (3) is: the mol ratio of organo-aluminium compound and described external electron donor compound is 0.1～500, and is preferred 1～300, more preferably 3～100.
The polymerization of alkene is carried out according to currently known methods, in liquid monomer or monomer in the liquid phase of the solution in inert solvent, or in gas phase, or by operating in the polymerization mix technology of gas-liquid in mutually.Polymerization temperature is generally 0 ℃～150 ℃, preferably 60 ℃～100 ℃.Polymerization pressure is a normal pressure or higher.
Embodiment
Provide following examples so that the present invention is described better rather than restriction the present invention.
The common step of propylene polymerization:
In 5 liters of autoclaves, adopt stream of nitrogen gas to purge 1 hour down, at room temperature introduce the hexane solution (concentration of triethyl aluminum is 0.5mmol/ml) of 5ml triethyl aluminum, hexane solution (concentration of CHMMS is 0.1mmol/ml), 10ml anhydrous hexane and the 9mg ingredient of solid catalyst of 1ml cyclohexyl methyl dimethoxy silane (CHMMS) in the stream of nitrogen gas then at 70 ℃.Close autoclave, introduce the hydrogen of 1.5NL and the liquid propene of 1.5Kg; In under agitation 5 minutes temperature is risen to 70 ℃., stop stirring after 1 hour 70 ℃ of following polyreactions, remove unpolymerized propylene monomer, collected polymer 70 ℃ of following vacuum-dryings 2 hours, is weighed and is calculated catalyst activity (AC); With the degree of isotacticity (I.I) of boiling n-heptane extraction process mensuration polymkeric substance, measure the melting index (M.I) of polymkeric substance by testing standard GB/T3682-2000.It is mensuration (standard specimen: PS, flow velocity: 1.0ml/min, the pillar: 3 * Pigel10um M1 * ED-B 300 * 7.5nm) of solvent under 150 ℃ with the trichlorobenzene that molecular weight distribution MWD (MWD=Mw/Mn) adopts PL-GPC220.
Electron donor compound of the present invention---the preparation of compd A:
Embodiment 1,9, two (benzoyloxy methyl) fluorenes of 9-synthetic
Synthetic (preparation method is referring to the CN1141285A) of (1) 9,9-dihydroxymethyl fluorenes
(DMSO uses CaH to add the 60ml methyl-sulphoxide in 9g (0.3mol) Paraformaldehyde 96 (vacuum hydro-extraction 8h)
2Dewater) and 0.4gNa and the 8ml dehydrated alcohol alcohol sodium solution after having reacted, the cooling of ice desire.Stir and in 30 seconds, add the DMSO solution that 100ml contains 16.6g fluorenes (0.1mol, vacuum hydro-extraction 8h) down, reaction 10min.
Add the hydrochloric acid termination reaction, and make solution become neutral, be poured in the 300ml saturated aqueous common salt, use ethyl acetate extraction, tell organic phase, saturated common salt washing 2 times, anhydrous sodium sulfate drying.Remove and to desolvate, the toluene recrystallization, white solid 9,9-dihydroxymethyl fluorenes, productive rate 72%, m.p.142～145 ℃.
1H NMR (δ, CDCl
3, ppm, TMS): 0.27 (t, 2H, hydroxyl hydrogen); (4.03 t, 4H, methylene radical hydrogen); 7.3～7.9 (m, 8H, aromatic ring hydrogen)
Synthesizing of two (benzoyloxy methyl) fluorenes of (2) 9,9-
In (1) of above-mentioned preparation 11.3g (0.05mol), add the 50ml tetrahydrofuran (THF), under agitation add 12.1ml (0.15mol) pyridine.Slowly add 14.5ml (0.125mol) Benzoyl chloride after stirring evenly, stirring at room 1h, reflux 4h then.
Add the salt that the 70ml water dissolution generates, organic phase is told in the toluene extraction, saturated common salt washing 2 times, anhydrous sodium sulfate drying.Remove and desolvate, get white solid.Use re-crystallizing in ethyl acetate, white crystal 9, two (benzoyloxy methyl) fluorenes of 9-, yield 89%, m.p.144～146 ℃.
1H NMR (δ, CDCl
3, ppm, TMS): 4.74 (s, 4H, methylene radical hydrogen); 7.25～7.75 (m, 18H, aromatic ring hydrogen).
Embodiment 2,2-sec.-propyl-2-isopentyl-1, ammediol hexichol first carboxylic ester synthetic
(1) synthetic (preparation method is referring to the CN1036846C) of 2-sec.-propyl-5-methyl-2-hexenoic aldehyde.
The Amberlite IRA910 resin (Rohm﹠amp of the OH-form of the isovaleric aldehyde of 207g and 26ml; Hass produces) reflux.Remove the water of generation with water trap, collect stopped reaction behind about 26ml water, filter out resin.Underpressure distillation, the cut of 85～90 ℃/20mmHg of collection.
(2) 2-sec.-propyl-5-methyl hexanal is synthetic
Add 70ml ethanol, the saturated NaHCO of 1ml in above-mentioned synthetic 10g 2-sec.-propyl-5-methyl-2-hexenoic aldehyde
3The Pd of 10% on solution and the 0.25g carbon support.Feed N
2, feed H then
2, install and be with the graduated H of being full of
2Drop-burette link to each other.The normal temperature and pressure stirring reaction is up to H
2Absorption reach calculated value.Filter, filtrate is used for secondary response down.
(3) 2-sec.-propyl-2-isopentyl-1, ammediol synthetic
Add 5.3gK in the above-mentioned filtrate
2CO
3Be dissolved in the solution of 13.1ml water and the CH of 16.9ml 60%
2O, reflux 7h.Remove ethanol, tell organic phase and hot water wash up to neutrality.Underpressure distillation gets 2-sec.-propyl-2-isopentyl-1, ammediol, b.p.165 ℃/20mmHg.
(4) 2-sec.-propyl-2-isopentyl-1, ammediol hexichol first carboxylic ester synthetic
9.4g (0.05mol) 2-sec.-propyl-2-isopentyl-1 adds the 50ml tetrahydrofuran (THF) in the ammediol, under agitation add 12.1ml (0.15mol) pyridine.Slowly add 14.5ml (0.125mol) Benzoyl chloride after stirring evenly, stirring at room 1h, reflux 4h then.
Add the salt that the 70ml water dissolution generates, ethyl acetate extraction is told organic phase, saturated common salt washing 2 times, anhydrous sodium sulfate drying.Remove and desolvate, underpressure distillation gets light yellow liquid 2-sec.-propyl 2-isopentyl-1, ammediol hexichol first carboxylic ester, yield 91%.
1H NMR (δ, CDCl
3, ppm, TMS): 0.88 (d, 6H, the methyl hydrogen of isopentyl); (1.05 d, 6H, the methyl hydrogen of sec.-propyl); (1.24 m, 2H, the methylene radical hydrogen of isopentyl); (1.27 m, 2H, the methylene radical hydrogen of isopentyl); (1.58 m, 1H, the methyne hydrogen of isopentyl); (2.04 m, 1H, the methyne hydrogen of sec.-propyl); (4.42 m, 4H, 1, the methoxyl group hydrogen of ammediol); 7.38～8.02 (m, 10H, aromatic ring hydrogen).
Embodiment 3,2, the preparation of 4-pentanediol dibenzoate
The preparation of (1) 2,4-pentanediol
10g2,4-diacetylmethane and 30ml methanol mixture are added drop-wise under 0～10 ℃ in the mixing solutions of 2.5g sodium borohydride, 0.1g sodium hydroxide and 25ml water.Finish, removal of solvent under reduced pressure is with 40ml ethyl acetate continuous extraction 15h.Remove and desolvate, column chromatography gets colourless liquid 2,4-pentanediol, yield 90%.
The preparation of (2) 2,4-pentanediol dibenzoates
0.03mol 2, add 30ml tetrahydrofuran (THF) and 0.09mol pyridine in the 4-pentanediol, under agitation add the 0.075mol Benzoyl chloride, reflux 4h.The cooling back adds 20ml saturated aqueous common salt, ethyl acetate extraction, anhydrous Na
2SO
4Drying is removed and is desolvated.Column chromatography or underpressure distillation get colourless liquid 2,4-pentanediol dibenzoate, yield 95%.
1H NMR (δ, ppm, TMS): 1.3～1.4 (8H, m, methyl H); 2.0～2.1 (2H, m, methylene radical H); 5.2～5.3 (2H, m, the methyne H of ester group); 7.3～8.0 (10H, m, phenyl ring H).
Embodiment 4,4-ethyl-3, the preparation of 5-heptanediol dibenzoate
(1) 4-ethyl-3, the preparation of 5-heptadione
10.2g 3, the mixture of 5-heptadione, iodoethane and 80mlTHF under agitation adds 50% sodium hydride oily matter 4.8g in batches.Finish, stir heating reflux reaction 8h down.Remove and desolvate, get 4-ethyl-3, the 5-heptadione.
(2) 4-ethyl-3, the preparation of 5-heptanediol
14.6g 3,5-heptadione and 30ml methanol mixture are added drop-wise under 0～10 ℃ in the mixing solutions of 3.1g sodium borohydride, 0.06g sodium hydroxide and 25ml water.Finish, removal of solvent under reduced pressure is with 40ml ethyl acetate continuous extraction 15h.Remove and desolvate, get product, yield 90%.The IR spectrogram is at 3400cm
-1There is strong absorption peak at the place, and at 1700cm
-1About do not have absorption peak, prove that reduction reaction carries out fully.
(2) 4-ethyl-3, the preparation of 5-heptanediol dibenzoate
4.4g 4-ethyl-3, add 50ml tetrahydrofuran (THF) and 9ml pyridine in the 5-heptanediol, under agitation add the 10g Benzoyl chloride, reflux 4h.The cooling back adds 20ml saturated aqueous common salt, ethyl acetate extraction, anhydrous Na
2SO
4Drying is removed and is desolvated.Column chromatography gets colourless viscous liquid 4-ethyl-3,5-heptanediol dibenzoate, yield 92%
1H NMR(δ，ppm，TMS)：7.4～7.8(10H，m，ArH)；5.1～5.3(2H，m，-CHCO)；2.0(1H，m，CH)；1.8～1.9(2H，dt，CH
2)；1.6～1.7(4H，q，CH
2)；0.9～1.0(9H，m，CH
3)。
Embodiment 5～28 is the preparation of ingredient of solid catalyst:
The common step of ingredient of solid catalyst preparation:
In the glass reaction bottle that the 350ml band stirs, add the 100ml titanium tetrachloride, be cooled to-10 ℃～-20 ℃.Adding the spherical magnesium chloride alcohol of 7g adds and thing (MgCl
22.8C
2H
5OH, its preparation method is referring to Chinese patent CN1330086A), slowly be warming up to 100 ℃ stage by stage then, wherein when being warming up to 40 ℃～80 ℃, add electron donor compound (B), system filters liquid at 100 ℃ after keeping 0.5～2.0 hour; Add 100ml toluene afterwards, be warming up to 100 ℃, wherein add electron donor compound (A) when being warming up to 40 ℃～80 ℃, system filters liquid at 100 ℃ after keeping 0.5～2.0 hour; Add 40ml toluene and 60ml titanium tetrachloride afterwards, filter liquid after keeping 1 hour at 80 ℃; Use the hexane wash solids then, 60 ℃ of heat are washed 2 times, and room temperature cold wash 2 times, hexane consumption are 60ml/ time.Vacuumize the drying solid thing at last, promptly obtain ingredient of solid catalyst of the present invention.
Embodiment 5～28 the results are shown in the table 1.
Table 1
| The embodiment numbering | Electron donor compound (A) | Electron donor compound (B) | AC | II | MWD | ||
| Title | Add-on (mmol) | Title | Add-on (mmol) | kgPP/gCat.h | wt％ | ||
| 5 | 2-sec.-propyl-2-isopentyl-1, the ammediol dibenzoate | 2.5 | DNBP | 3.9 | 55 | 97.9 | 8.5 |
| 6 | 2-sec.-propyl-2-isopentyl-1, the ammediol dibenzoate | 0.78 | DNBP | 3.9 | 57 | 98.0 | 8.9 |
| 7 | 2-sec.-propyl-2-isopentyl-1, the ammediol dibenzoate | 0.51 | DNBP | 3.9 | 57 | 98.0 | 8.7 |
| 8 | 2-sec.-propyl-2-isopentyl-1, the ammediol dibenzoate | 0.38 | DNBP | 3.9 | 58 | 98.3 | 9.4 |
| 9 | 2-sec.-propyl-2-isopentyl-1, the ammediol dibenzoate | 0.25 | DNBP | 3.9 | 60 | 97.8 | 8.9 |
| 10 | 2,4-pentanediol dibenzoate | 2.5 | DNBP | 3.9 | 55 | 98.3 | 6.8 |
| 11 | 2,4-pentanediol dibenzoate | 0.78 | DNBP | 3.9 | 60 | 98.5 | 6.6 |
| 12 | 2,4-pentanediol dibenzoate | 0.51 | DNBP | 3.9 | 60 | 98.5 | 6.7 |
| 13 | 2,4-pentanediol dibenzoate | 0.38 | DNBP | 3.9 | 66 | 98.3 | 6.3 |
| 14 | 2,4-pentanediol dibenzoate | 0.25 | DNBP | 3.9 | 70 | 98.4 | 6.5 |
| 15 | 4-ethyl-3,5-heptanediol dibenzoate | 2.5 | DNBP | 3.9 | 57 | 98.0 | 6.9 |
| 16 | 4-ethyl-3,5-heptanediol dibenzoate | 0.78 | DNBP | 3.9 | 61 | 98.6 | 6.7 |
| 17 | 4-ethyl-3,5-heptanediol dibenzoate | 0.51 | DNBP | 3.9 | 65 | 98.4 | 6.4 |
| 18 | 4-ethyl-3,5-heptanediol dibenzoate | 0.38 | DNBP | 3.9 | 65 | 98.5 | 5.9 |
| 19 | 4-ethyl-3,5-heptanediol dibenzoate | 0.25 | DNBP | 3.9 | 69 | 98.3 | 5.9 |
| 20 | 9, two (benzoyloxy methyl) fluorenes of 9- | 2.5 | DNBP | 3.9 | 49 | 97.8 | 7.9 |
| 21 | 9, two (benzoyloxy methyl) fluorenes of 9- | 0.78 | DNBP | 3.9 | 53 | 98.2 | 7.6 |
| 22 | 9, two (benzoyloxy methyl) fluorenes of 9- | 0.51 | DNBP | 3.9 | 55 | 98.1 | 8.4 |
| 23 | 9, two (benzoyloxy methyl) fluorenes of 9- | 0.38 | DNBP | 3.9 | 58 | 98.3 | 8.2 |
| 24 | 9, two (benzoyloxy methyl) fluorenes of 9- | 0.25 | DNBP | 3.9 | 59 | 98.5 | 8.3 |
| 25 | 2-sec.-propyl-2-isopentyl-1, the ammediol dibenzoate | 0.38 | DIBP | 3.9 | 57 | 98.2 | 9.3 |
| 26 | 2,4 gas pentanediol dibenzoates | 0.38 | DIBP | 3.9 | 63 | 98.0 | 6.3 |
| 27 | 4-ethyl-3,5-heptanediol dibenzoate | 0.38 | DIBP | 3.9 | 60 | 97.9 | 6.2 |
| 28 | 9, two (benzoyloxy methyl) fluorenes of 9- | 0.38 | DIBP | 3.9 | 55 | 97.7 | 7.9 |
| Comparative Examples | Do not have | Do not have | DNBP | 3.9 | 50 | 98.1 | 4.1 |
Annotate: DNBP---n-butyl phthalate: DIBP---diisobutyl phthalate
From table 1 embodiment and the data of Comparative Examples more as can be seen, after having used two kinds of electron donor compounds in the present invention activity of such catalysts is reduced, but also be significantly improved, the molecular weight distribution of resulting polymers also has raising significantly simultaneously.
Claims (12)
1, the catalyst component that is used for olefinic polymerization, this catalyst component comprise titanium, magnesium, halogen and at least two kinds of electron donor compd As and B, and wherein the electron donor compd A is selected from the polyol ester compounds shown in general formula (I):
R in the formula
1-R
6, R
1-R
2nGroup is hydrogen, halogen or the replacement identical or inequality or the C of unsubstituted straight or branched
1-C
20Alkyl, C
3-C
20Cycloalkyl, C
6-C
20Aryl, C
7-C
20Alkaryl, C
7-C
20Aralkyl, C
2-C
10Alkylene, C
10-C
20Fused ring aryl or C
2-C
10Ester group; But R
1And R
2Not hydrogen, R
3-R
6And R
1-R
2nComprise one or several heteroatoms on the group arbitrarily as carbon or hydrogen atom or both substituents, described heteroatoms is selected from nitrogen, oxygen, sulphur, silicon, phosphorus or halogen atom, R
3-R
6And R
1-R
2nOne or more in the group can link up into ring; N is the integer of 0-10;
The electron donor compd B is selected from ester, ether, ketone, amine and the silane compound except that compd A.
2, the catalyst component that is used for olefinic polymerization according to claim 1, wherein the electron donor compd A is selected from the polyester compounds shown in general formula (II):
R wherein
1-R
6, R
1-R
2Definition in group such as the general formula (I).
3, the catalyst component that is used for olefinic polymerization according to claim 1 and 2, in the polyol ester compounds shown in its formula of (I) or the general formula (II), R
3, R
4, R
5, R
6Be not hydrogen simultaneously, and R
3, R
4, R
5And R
6In have at least a group to be selected from halogen, C
1-C
10The alkyl of straight or branched, C
3-C
10Cycloalkyl, C
6-C
10Aryl, C
7-C
10Alkaryl or aralkyl.
4, the catalyst component that is used for olefinic polymerization according to claim 1, wherein the electron donor compd A is selected from the polyol ester compounds shown in general formula (III):
R wherein
1-R
2Definition in group such as the general formula (I); R ' is the C of hydrogen identical or inequality, halogen atom, straight or branched
1-C
20Alkyl, C
3-C
20Cycloalkyl, C
6-C
20Aryl, C
7-C
20Alkaryl or C
7-C
20Aralkyl.
5, the catalyst component that is used for olefinic polymerization according to claim 1, in the wherein said polyol ester compounds, R
1And R
2In have at least one to be selected from phenyl, halogenated phenyl, alkyl phenyl or halogenated alkyl phenyl.
6, the catalyst component that is used for olefinic polymerization according to claim 1, wherein said electron donor compd B are selected from monobasic or polyhydric aliphatic family carboxylicesters or aromatic carboxylic acid esters and diether compound.
7, the catalyst component that is used for olefinic polymerization according to claim 6, wherein said monobasic or polyhydric aliphatic family carboxylicesters or aromatic carboxylic acid esters comprise benzoates, phthalate, malonic ester class, succinate class, glutarate class or pivalate compounds.
8, the catalyst component that is used for olefinic polymerization according to claim 6, wherein said diether compound are 1 shown in the general formula (IV), 3-two ethers:
R wherein
I, R
II, R
III, R
IV, R
VAnd R
VIMutually the same or inequality, be selected from the C of hydrogen, halogen atom, straight or branched
1-C
20Alkyl, C
3-C
20Cycloalkyl, C
6-C
20Aryl, C
7-C
20Alkaryl, C
7-C
20A kind of in the aralkyl, and R
VIIAnd R
VIIICan be identical or different, be selected from the C of straight or branched
1-C
20Alkyl, C
3-C
20Cycloalkyl, C
6-C
20Aryl, C
7-C
20Alkaryl, C
7-C
20A kind of in the aralkyl; R
I-R
VIGroup between can be keyed to ring.
9, the catalyst component that is used for olefinic polymerization according to claim 1 is characterized in that the mol ratio of described two kinds of electron donor compd As and B is 0.01-0.5.
10 catalyst components that are used for olefinic polymerization according to claim 1 is characterized in that this catalyst component is at a kind of MgCl
2.nROH load has titanium compound with at least one Ti-halogen bond and the reaction product of described two kinds of electron donor compd As and B on the adducts, and wherein n is 1.5～4; R is the alkyl of carbon number 1-4.
11, a kind of CH that is used for
2The catalyzer of=CHR olefinic polyreaction, wherein R is hydrogen or C
1-C
6Alkyl or aryl, comprise the reaction product of following component:
(1) the described catalyst component of one of claim 1-10;
(2) alkylaluminium cpd;
(3) randomly, external electron donor component.
12, be used for alkene CH
2=CHR polymeric method, wherein R is the hydrocarbyl group of hydrogen or 1-12 carbon atom, carries out in the presence of the described catalyzer of claim 11.
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| CNB2004100736238A CN100338103C (en) | 2004-09-02 | 2004-09-02 | Catalyst component for olefinic polymerization and its catalyst |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2004100736238A CN100338103C (en) | 2004-09-02 | 2004-09-02 | Catalyst component for olefinic polymerization and its catalyst |
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| CN100338103C CN100338103C (en) | 2007-09-19 |
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