U.S. patent application number 09/804025 was filed with the patent office on 2001-07-26 for olefin polymer and process for producing the same.
This patent application is currently assigned to Sumitomo Chemical Company, Limited.. Invention is credited to Fujita, Masayuki, Miyatake, Tatsuya.
Application Number | 20010009953 09/804025 |
Document ID | / |
Family ID | 11897664 |
Filed Date | 2001-07-26 |
United States Patent
Application |
20010009953 |
Kind Code |
A1 |
Fujita, Masayuki ; et
al. |
July 26, 2001 |
Olefin polymer and process for producing the same
Abstract
An olefin polymer of an alkenyl hydrocarbon having 5 or more
carbon atoms, wherein said olefin polymer is an amorphous polymer
having a Mn of 300,000 and a Mw/Mn of 2.40 or less, and
substantially not having a melting point, and a process for
producing said olefin polymer which comprises polymerizing an
alkenyl hydrocarbon having 5 or more carbon atoms with an olefin
polymerization catalyst obtained by contacting: a specific
transition metal compound(A), an organoaluminumoxy compound (B)
soluble in an aromatic solvent and water (C).
Inventors: |
Fujita, Masayuki;
(Ichihara-shi, JP) ; Miyatake, Tatsuya;
(Ichihara-shi, JP) |
Correspondence
Address: |
BIRCH STEWART KOLASCH & BIRCH
PO BOX 747
FALLS CHURCH
VA
22040-0747
US
|
Assignee: |
Sumitomo Chemical Company,
Limited.
|
Family ID: |
11897664 |
Appl. No.: |
09/804025 |
Filed: |
March 13, 2001 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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09804025 |
Mar 13, 2001 |
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09237798 |
Jan 27, 1999 |
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6232421 |
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Current U.S.
Class: |
526/161 ;
526/172; 526/348.2; 526/348.5; 526/348.6 |
Current CPC
Class: |
C08F 110/14 20130101;
C08F 10/14 20130101; C08F 10/14 20130101; C08F 4/64165 20130101;
C08F 110/14 20130101; C08F 2500/03 20130101; C08F 2500/01 20130101;
C08F 10/14 20130101; C08F 4/64079 20130101 |
Class at
Publication: |
526/161 ;
526/172; 526/348.2; 526/348.5; 526/348.6 |
International
Class: |
C08F 010/14 |
Foreign Application Data
Date |
Code |
Application Number |
Jan 28, 1998 |
JP |
10-015757 |
Claims
What is claimed is:
1. A process for producing an olefin polymer of an alkenyl
hydrocarbon having 5 or more carbon atoms, wherein said olefin
polymer has a polystyrene-reduced number average molecular weight
of 300,000 or more, and a molecular weight distribution of 2.40 or
less in terms of ratio of polystyrene-reduced weight average
molecular weight to polystyrene-reduced number average molecular
weight, and is an amorphous polymer substantially not having a
melting point, comprising: polymerizing an alkenyl hydrocarbon
having 5 or more carbon atoms with an olefin polymerization
catalyst obtained by contacting: a transition metal compound (A)
represented by the formula (1) described below; 5wherein, M
represents a transition metal atom of the Fourth Group of the
Periodic Table; X and Y independently represent a hydrogen atom, a
halogen atom, an alkyl group, an aryl group, an aralkyl group, an
alkoxy group, an aryloxy group, an aralkyloxy group, a sulfonyloxy
group, a di-substituted amino group or a substituted silyl group;
R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7 and
R.sup.8 independently represent a hydrogen atom, an alkyl group, an
aryl group, an aralkyl group, an alkoxy group, an aryloxy group, an
aralkyloxy group, a di-substituted amino group or a substituted
silyl group; R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7
and R.sup.8 may be optionally bonded to form a ring; T represents a
divalent covalent crosslinking group having 1 to 20 carbon atoms,
or a divalent group represented by --O--, --S--, --S--S--,
--S(.dbd.O)--, --S(.dbd.O).sub.2--, --C(.dbd.O)--, --N(R.sup.9)--,
--P(R.sup.9)-- or --P(.dbd.O) (R.sup.9)--, wherein R.sup.9
represents a hydrogen atom or a hydrocarbon group having 1 to 6
carbon atoms; and n is an integer of from 0 to 3; an
organoaluminumoxy compound (B) soluble in an aromatic solvent; and
water (C), wherein the molar ratio of aluminum atom contained in
the organoaluminumoxy compound (B) to a transition metal atom
contained in the transition metal compound (A) is 1 to 20000, and
the amount of water used is 0.1 to 3.0 mol per aluminum atom
contained in the organoaluminumoxy compound (B).
2. The process according to claim 1, wherein T is a divalent group
represented by --S--.
3. The process according to claim 1, wherein the organoaluminumoxy
compound (B) soluble in an aromatic solvent is
methylisobutylalumoxane.
4. The process according to claim 1, wherein the organoaluminumoxy
compound (B) soluble in an aromtaic hydrocarbon solvent is an
organoaluminumoxy compound represented by formula (4) or (5):
6wherein R represents methyl group or isobutyl group, the presence
ratio of methyl group and isobutyl group is methyl group: isobutyl
group=5 to 95:95 to 5; Al represents aluminum atom; and m
represents a number of 1 to 5.
5. The process according to claim 1, wherein the amount of
organoaluminumoxy (B) is 100 to 20,000 mol in terms of aluminum
atom contained in the organoaluminumoxy compound per one mol of the
transition metal atom contained the the transition metal compound
(A) and the amount of the water (C) is 0.1 to 1.0 mol per one mol
of an aluminum atom contained in the organoaluminumoxy compound
(B).
6. The process according to claim 1, wherein the alkenyl
hydrocarbon having 5 or more carbon atoms is 1-hexene or 1-octene.
Description
BACKGROUND OF THE INVENTION
[0001] 1. Field of the Invention
[0002] The present invention relates to a specified amorphous
polymer and a process for producing the same. More specifically,
the present invention relates to an amorphous polymer having a high
molecular weight enough to improve problems such as stickiness,
elution to an organic solvent and the like, and to exhibit an
elastomeric property and substantially not having a melting point
and a process for producing said amorphous polymer.
[0003] 2. Description of Related Arts
[0004] An amorphous poly(.alpha.-olefin)(for example, an atactic
polypropylene and an atactic poly(1-butene)) has been mainly used
as a sticking agent, an improving agent for a crystalline
polyolefin and the like. However, the molecular weight of an
amorphous poly(.alpha.-olefin), as known well, is not high enough,
therefore the amorphous poly(.alpha.-olefin) has problems such as
stickiness of a product, elution to an organic solvent and the
like, and it is difficult to say that an elastomeric property is
sufficiently exhibited.
[0005] With respect to a synthesis of the amorphous polymer, Some
processes have been known. It has been known from old times that a
low-crystalline polymer prepared as a by-product is recovered when
an olefin is polymerized with a solid Ziegler-Natta catalyst and an
isotactic polymer is produced. However, the polymer obtained then
has a low molecular weight and wide molecular weight distribution,
and there have been problems such as stickiness of a product,
elution to an organic solvent and the like.
[0006] Further, there are a report (Chem. Commun., 1996, 783) in
which a high molecular weight poly(1-hexene)(Mn=1,252,000,
Mw/Mn=2.70) can be synthesized by polymerizing 1-hexene under a
ultra-high pressure of 250 Mpa with a catalyst composed of using a
hafnocene dichloride compound and methyl aluminoxane, and a report
(EP0604917 A2 and EP0604908 A2) in which a polypropylene having a
weight average molecular weight Mw of 377,000, a molecular weight
distribution Mw/Mn(number average molecular weight) of 2.64 and a
viscosity [.eta.] of 2.28 dl/g, and a poly(1-butene) having a
viscosity [.eta.] of 1.29 dl/g, can be synthesized by polymerizing
propylene with a catalyst composed of dimethylsilylene
bis(9-fluorenyl) zirconium dichloride and methyl alumoxane, but a
polymer having an adequate high molecular weight and narrow
molecular weight distribution is not obtained.
[0007] On the other hand, a polymer having a Mw of more than
8.times.10.sup.6 can be synthesized (Macromolecular Chemie, Rapid
Communication, Vol.10 (1989), page 349) by polymerizing propylene
using a transition metal compound having an aryloxy ligand as a
catalyst component, but the glass transition temperature of the
polymer was somewhat high and an elastomeric property was not
sufficient. Further, in the polymerization of an olefin having 5 or
more carbon atoms with such catalyst, the resulted polymer was also
not always satisfactory in the points of stickiness and elution
property to an organic solvent.
[0008] As described above, a poly(.alpha.-olefin of 5 or more
carbon atoms) which has an adequate high molecular weight and
narrow molecular weight distribution and no melting point
substantially, and is amorphous, is not obtained.
SUMMARY OF THE INVENTION
[0009] An object of the present invention is to provide an
amorphous polymer having a high molecular weight enough to improve
problems such as stickiness, elution to an organic solvent and the
like, and to exhibit an elastomeric property, and substantially not
having a melting point.
[0010] Another object of the present invention to provide a process
for producing said amorphous polymer.
[0011] Other objects and advantages of the present invention will
be apparent from description below.
[0012] The present inventors have intensively studied to attain the
above-mentioned objects, and as a result, completed the present
invention.
[0013] According to the present invention, there are provided an
olefin polymer of an alkenyl hydrocarbon having 5 or more carbon
atoms, wherein said olefin polymer is an amorphous polymer having a
polystyrene-reduced number average molecular weight of 300,000 and
a molecular weight distribution of 2.40 or less in terms of a ratio
of polystyrene-reduced weight average molecular weight
(hereinafter, sometimes referred to as "Mw") to polystyrene-reduced
number average molecular weight(hereinafter, sometimes referred to
as "Mn") [Mw/Mn], and substantially not having a melting point, and
a process for producing said olefin polymer which comprises
polymerizing an alkenyl hydrocarbon having 5 or more carbon atoms
with an olefin polymerization catalyst obtained by contacting:
[0014] a transition metal compound (A) represented by the general
formula (1) described below;
[0015] an organoaluminumoxy compound (B) soluble in an aromatic
solvent; and
[0016] water (C), wherein the molar ratio of aluminum atom
contained in the organoaluminumoxy compound (B) to a transition
metal atom contained in the transition metal compound (A) is 1 to
20000, and the amount of water used is 0.1 to 3.0 mol per 1 mol of
aluminum atom contained in the organoaluminumoxy compound (B).
1
[0017] (wherein M represents a transition metal atom of the Fourth
Group of the Periodic Table, X and Y independently represent a
hydrogen atom, a halogen atom, an alkyl group, an aryl group, an
aralkyl group, an alkoxy group, an aryloxy group, an aralkyloxy
group, a sulfonyloxy group, a di-substituted amino group or a
substituted silyl group. R.sup.1, R.sup.2, R.sup.3, R.sup.4,
R.sup.5, R.sup.6, R.sup.7 and R.sup.8 independently represent a
hydrogen atom, an alkyl group, an aryl group, an aralkyl group, an
alkoxy group, an aryloxy group, an aralkyloxy group, a
di-substituted amino group or a substituted silyl group. Further,
R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7 and
R.sup.8 may be optionally bonded to form a ring. T represents a
divalent covalent crosslinking group having 1 to 20 carbon atoms,
or a divalent group represented by --O--, --S--, --S--S--,
--S(.dbd.O)--, --S(.dbd.O).sub.2--, --C(.dbd.O)--, --N(R.sup.9)--,
--P(R.sup.9)--, or --P(.dbd.O)(R.sup.9)-- (wherein R.sup.9
represents a hydrogen atom or a hydrocarbon group having 1 to 6
carbon atoms in each case), n is an integer of from 0 to 3.).
BRIEF DESCRIPTION OF THE DRAWING
[0018] FIG. 1 is a flow chart to aid the understanding of the
present invention. The flow chart is a representative example of
the mode of operation of the present invention, and the present
invention is not limited thereto.
DETAILED DESCRIPTION OF THE INVENTION
[0019] The present invention is explained in detail below.
[0020] An olefin polymer of the present invention is a polymer of
an alkenyl hydrocarbon having 5 or more carbon atoms and an
amorphous polymer having a Mn of 300,000 or more and a Mw/Mn of
2.40 or less, and substantially not having melting point.
[0021] Specific examples of the alkenyl hydrocarbon having 5 or
more carbon atoms, include an .alpha.-olefin having 5 or more
carbon atoms such as 1-pentene, 1-hexene, 3-methyl-1-pentene,
3-ethyl-1-penetene, 4-methyl-1-penete, 1-octene, 1-decene,
1-dodecene, 1-tetradecene and the like, and vinylcyclohexane, and
the like, and an alkenyl hydrocarbon having 5 to 20 carbon atoms is
preferred. As the alkenyl hydrocarbon having 5 or more carbon
atoms, a linear .alpha.-olefin is more preferable, and 1-hexene or
1-octene is most preferable.
[0022] The olefin polymer of the present invention may be a
copolymer. As a comonomer constituting the copolymer, a monomer
copolymerizable with the alkenyl hydrocarbon having 5 or more
carbon atoms, excluding 1-butene, can be used, and propylene or
another alkenyl hydrocarbon having 5 or more carbon atoms is
preferable.
[0023] The content of the alkenyl hydrocarbon having 5 or more
carbon atoms in the polymer of the present invention is preferably
20 mol % or more, more preferably 50 mol % or more, and
particularly preferable 70 mol % or more. Further, the most
preferable olefin polymer of the present invention is a homopolymer
of 1-hexene (poly(1-hexene)) or a homopolymer of 1-octene
(poly(1-octene)).
[0024] The Mn of the olefin polymer of the present invention is
300,000 or more, preferably 500,000 or more, and more preferably
800,000 or more. When the Mn of the olefin polymer is less than
300,000, it is not preferable because problems such as stickiness
and elution to an organic solvent sometimes happen to occur.
[0025] Herein, the Mn described above and Mw described below mean a
polystyrene-reduced number average molecular weight and a
polystyrene-reduced weight average molecular weight, respectively,
measured by gel permeation chromatography method.
[0026] The olefin polymer of the present invention has a Mw/Mn of
2.40 or less, preferably 2.3 or less, and more preferably 2.2 or
less. When the Mw/Mn exceeds 2.40, it is not preferable because
problems such as stickiness and elution to an organic solvent
sometimes happen to occur.
[0027] The olefin polymer of the present invention is an amorphous
polymer substantially not having a melting point. The melting point
is usually measured with a differential scanning calorimeter (DSC)
or the like. In the present invention, the term "substantially not
having a melting point" means that a crystal melting peak or
crystallization peak is not substantially observed in the DSC
measurement.
[0028] Such olefin polymer can be produced using, for example, said
olefin polymerization catalyst obtained by contacting a transition
metal compound (A) represented by the general formula (1) described
above, an organoaluminumoxy compound (B) soluble in an aromatic
solvent, and water (C).
[0029] In the fore-mentioned general formula (1), M represents a
transition metal atom of the Fourth Group of the Periodic Table
(IUPAC Inorganic Chemistry Nomenclature, a revised edition, 1989)
of elements, and a titanium atom, a zirconium atom or a hafnium
atom is preferable and a titanium atom is more preferable.
[0030] In the general formula (1), respective X and Y independently
represent a hydrogen atom, a halogen atom, an alkyl group, an aryl
group, an aralkyl group, an alkoxy group, an aryloxy group, an
aralkyloxy group, a sulfonyloxy group, a di-substituted amino group
or a substituted silyl group.
[0031] Specific examples of such halogen atoms include a chlorine
atom, a bromine atom, an iodine atom and the like, and a chlorine
atom is preferable.
[0032] As the alkyl group in X or Y of the above-mentioned general
formula (1), an alkyl group hydrocarbon having 1 to 24 carbon atoms
is preferable. Specific examples thereof include methyl group,
ethyl group, n-propyl group, isopropyl group, n-butyl group,
sec-butyl group, tert-butyl group, n-pentyl group, neo-pentyl
group, iso-pentyl group, 1-methylbutyl group, n-hexyl group,
n-octyl group, n-decyl group, n-dodecyl group, n-pentadecyl group,
n-eicosyl group, and the like. Methyl group, ethyl group, isopropyl
group, tert-butyl group, n-pentyl group, neo-pentyl group or
iso-pentyl group is preferable.
[0033] Any one of these alkyl groups may be substituted with
halogen atoms such as a fluorine atom, chlorine atom, bromine atom
and iodine atom, alkoxy groups such as methoxy group, ethoxy group
and the like, and aryloxy groups such as phenoxy group and the
like.
[0034] Examples of the alkyl group having 1 to 24 carbon atoms
which is substituted with a halogen atom include a fluoromethyl
group, a difluoromethyl group, trifluoromethyl group, a
chloromethyl group, a dichloromethyl group, trichloromethyl group,
a bromomethyl group, a dibromomethyl group, tribromomethyl group,
an iodomethyl group, a diiodomethyl group, triiodomethyl group, a
fluoroethyl group, a difluoroethyl group, a trifluoroethyl group, a
tetrafluoroethyl group, pentafluoroethyl group, a chloroethyl
group, a dichloroethyl group, a trichloroethyl group, a
tetrachloroethyl group, pentachloroethyl group, a bromoethyl group,
a dibromoethyl group, a tribromoethyl group, a tetrabromoethyl
group, a pentabromoethyl group, a perfluoropropyl group, a
perfluorobutyl group, a perfluoropentyl group, a perfluorohexyl
group, a perfluorooctyl group, a perfluorododecyl group, a
perfluoropentadecyl group, a perfluoroeicosyl group, a
perchloropropyl group, a perchlorobutyl group, a perchloropentyl
group, a perchlorohexyl group, a perchlorooctyl group, a
perchlorododecyl group, a perchloropentadecyl group, a
perchloroeicosyl group, a perbromopropyl group, a perbromobutyl
group, a perbromopentyl group, a perbromohexyl group, a
perbromooctyl group, a perbromododecyl group, a perbromopentadecyl
group, a perbromoeicosyl group, and the like. When various isomers
exist, such isomers are included.
[0035] Further, as the aryl group in X or Y in the general formula
(1) described above, an aryl group having 6 to 24 carbon atoms is
preferable, and specific examples thereof include phenyl group,
2-tolyl group, 3-tolyl group, 4-tolyl group, a 2,3-xylyl group, a
2,4-xylyl group, 2,5-xylyl group, 2,6-xylyl group, 3,4-xylyl group,
3,5-xylyl group, 2,3,4-trimethylphenyl group, 2,3,5-trimethylphenyl
group, 2,3,6-trimethylphenyl group, 2,4,6-trimethylphenyl group,
3,4,5-trimethylphenyl group, 2,3,4,5-tetramethylphenyl group,
pentamethylphenyl group, an ethylphenyl group, a n-propylphenyl
group, a iso-propylphenyl group, a n-butylphenyl group, a
sec-butylphenyl group, a tert-butylphenyl group, a n-pentylphenyl
group, a neo-pentylphenyl group, a n-hexylphenyl group, naphtyl
group, an antharcenyl group, and the like, and phenyl group is
preferable. Any one of these aryl groups may be substituted with a
halogen atom such as a fluorine atom, chlorine atom, bromine atom
or an iodine atom, an alkoxy group such as methoxy group, ethoxy
group or the like, and an aryloxy group such as phenoxy group or
the like.
[0036] As the aralkyl group in X or Y in the general formula (1)
described above, an aralkyl group having 7 to 24 carbon atoms is
preferable, and specific examples thereof include benzyl group,
(2-methylphenyl)methyl group, (3-methylphenyl)methyl group,
(4-methylphenyl)methyl group, (2,3-dimethylphenyl)methyl group,
(2,4-dimethylphenyl)methyl group, (2,5-dimethylphenyl)methyl group,
(2,6-dimethylphenyl)methyl group, (3,4-dimethylphenyl)methyl group,
(4,6-dimethylphenyl)methyl group, (2,4,6-trimethylphenyl)methyl
group, (pentamethylphenyl)methyl group, a (ethylphenyl)methyl
group, a (n-propylphenyl)methyl group, a (n-butylphenyl)methyl
group, a (sec-butylphenyl)methyl group, a (tert-butylphenyl)methyl
group, a (n-pentylphenyl) methyl group, a (neo-pentylphenyl)methyl
group, naphtylmethyl group, antharcenylmethyl group and the like,
and benzyl group is preferable. Any one of these aralkyl groups may
be substituted with a halogen atom such as a fluorine atom, a
chlorine atom, a bromine atom or an iodine, an alkoxy group such as
methoxy group, ethoxy group or the like, and an aryloxy group such
as phenoxy group or the like.
[0037] As the alkoxy group in X or Y in the general formula (1)
described above, an alkoxy group having 1 to 24 carbon atoms is
preferable, and specific examples thereof include methoxy group,
ethoxy group, n-propoxy group, isopropoxy group, n-butoxy group,
sec-butoxy group, tert-butoxy group, n-pentoxy group, neopentoxy
group, n-hexoxy group, n-octoxy group, n-dodecoxy group,
n-pentadecoxy group, n-icosoxy group, and the like, and methoxy
group, ethoxy group or tert-butoxy group is preferable.
[0038] Any one of these alkoxy groups may be substituted with a
halogen atom such as a fluorine atom, a chlorine atom, a bromine
atom, or an iodine atom.
[0039] Further, as the aryloxy group in X or Y in the general
formula (1) described above, an aryloxy group having 6 to 24 carbon
atoms is preferable and specific examples thereof include phenoxy
group, 2-methylphenoxy group, 3-methylphenoxy group,
4-methylphenoxy group, 2,3-dimethylphenoxy group,
2,4-dimethylphenoxy group, 2,5-dimethylphenoxy group,
2,6-dimethylphenoxy group, 3,4-dimethylphenoxy group,
3,5-dimethylphenoxy group, 2,3,4-trimethylphenoxy group,
2,3,5-trimethylphenoxy group, 2,3,6-trimethylphenoxy group,
2,4,5-trimethylphenoxy group, 2,4,6-trimethylphenoxy group,
3,4,5-trimethylphenoxy group, 2,3,4,5-tetramethylphenoxy group,
2,3,4,6-tetramethylphenoxy group, 2,3,5,6-tetramethylphenoxy group,
pentamethylphenoxy group, an ethylphenoxy group, a n-propylphenoxy
group, an isopropylphenoxy group, a n-butylphenoxy group, a
sec-butylphenoxy group, a tert-butylphenoxy group, a n-hexylphenoxy
group, a n-octylphenoxy group, a n-decylphenoxy group, a
n-tetradecylphenoxy group, a naphtoxy group, an antharcenoxy group
and the like. Phenoxy group is preferable. Any one of these aryloxy
groups may be substituted with a halogen atom such as a fluorine
atom, chlorine atom, bromine atom or iodine atom.
[0040] As the aralkyloxy group in X or Y in the above-mentioned
formula (1) described above, an aralkyloxy group having 7 to 24
carbon atoms is preferable , and specific examples thereof include
a benzyloxy group, (2-methylphenyl)methoxy group,
(3-methylphenyl)methoxy group, (4-methylphenyl)methoxy group,
(2,3-dimethylphenyl)methoxy group, (2,4-dimethylphenyl)methoxy
group, (2,5-dimethyphenyl )methoxy group,
(2,6-dimethylphenyl)methoxy group, (3,4-dimethylphenyl)methoxy
group, (3,5-dimethylphenyl)methoxy group,
(2,3,4-trimethylphenyl)methoxy group,
(2,3,5-trimethylphenyl)methoxy group,
(2,3,6-trimethylphenyl)methoxy group,
(2,4,5-trimethylphenyl)methoxy group, (2,4,6-trimethylphenyl)metho-
xy group, (3,4,5-trimethylphenyl)methoxy group,
(2,3,4,5-tetramethylphenyl- )methoxy group,
(2,3,5,6-tetramethylphenyl)methoxy group,
(pentamethylphenyl)methoxy group, an (ethylphenyl)methoxy group, a
(n-propylphenyl)methoxy group, an (isopropylphenyl)methoxy group, a
(n-butylphenyl)methoxy group, a (sec-butylphenyl)methoxy group, a
(tert-butylphenyl)methoxy group, a (n-hexylphenyl)methoxy group, a
(n-octylphenyl) methoxy group, a (n-decylphenyl)methoxy group, a
n-tetradecylphenyl)methoxy group, a naphtylmethoxy group, an
antharcenylmethoxy group and the like, and a benzyloxy group is
preferable. Any one of these aralkyloxyl groups may be substituted
with halogen atoms such as a fluorine atom, a chlorine atom, a
bromine atom or an iodine atom.
[0041] The sulfonyloxy group in X or Y in the general formula (1)
described above represents a group indicated by the general formula
R.sup.10SO.sub.3-- and represents a sulfonyloxy group having 1 to
24 carbon atoms which may be optionally substituted. Specific
examples thereof include those such as methanesulfonyloxy group,
ethanesulfonyloxy group, dodecylsulfonyloxy group or the like whose
R.sup.10 is an alkyl group, those such as a
trifluoromethanesulfonyloxy group or the like whose a part is
substituted with a halogen atom, those such as p-toluenesulfonyloxy
group or the like whose R.sup.10 is an aryl group, or the like.
[0042] As the di-substituted amino group in X or Y in the general
formula (1) described above, a di-substituted amino group having
2-24 carbon atoms which is substituted with two hydrocarbon groups
is preferable. Specific examples the hydrocarbon groups include
alkyl groups having 1 to 10 carbon atoms such as methyl group,
ethyl group, n-propyl group, isopropyl group, n-butyl group,
sec-butyl group, tert-butyl group, isobutyl group, n-pentyl group,
n-hexyl group, cyclohexyl group and the like, aryl groups such as
phenyl group and the like, etc. Examples of such di-substituted
amino group having 2 to 24 carbon atoms include dimethylamino
group, diethylamino group, di-n-propylamino group,
di-isopropylamino group, di-n-butylamino group, di-sec-butylamino
group, di-tert-butylamino group, di-n-octylamino group,
di-n-decylamino group, di-phenylamino group,
bis-trimethylsilylamino group, bis-tert-butyldimethylsilylamino
group and the like, and dimethylamino group or diethylamino group
is preferable.
[0043] As the substituted silyl group in X or Y in the general
formula (1) described above, a substituted silyl group having 1 to
24 carbon atoms, in other words, a silyl group substituted with a
hydrocarbon group is preferable. Examples of the hydrocarbon group
include, for example, alkyl groups having 1 to 10 carbon atoms
(e.g. methyl group, ethyl group, n-propyl group, isopropyl group,
n-butyl group, sec-butyl group, tert-butyl group, isobutyl group,
n-pentyl group, n-hexyl group, cyclohexyl group), aryl groups (e.g.
phenyl group). Examples of such silyl group having 1 to 24 carbon
atoms include a mono-substituted silyl group having 1 to 20 carbon
atoms such as methylsilyl group, ethylsilyl group, phenylsilyl
group or the like, a disubstituted silyl group having 2 to 20
carbon atoms such as dimethylsilyl group, diethylsilyl group,
diphenylsilyl group or the like, a trisubstituted silyl group
having 3 to 20 carbon atoms such as trimethylsilyl group,
triethylsilyl group, tri-n-propylsilyl group, tri-isopropylsilyl
group, tri-n-butylsilyl group, tri-sec-butylsilyl group,
tri-tert-butylsilyl group, tri-isobutylsilyl group,
tert-butyldimethylsilyl group, tri-n-pentylsilyl group,
tri-n-hexylsilyl group, tricyclohexylsilyl group, triphenylsilyl
group and the like, and trimethylsilyl group,
tert-butyldimethylsilyl group or triphenylsilyl group is
preferable.
[0044] Any hydrocarbon group of these substituted silyl groups may
be substituted with a halogen atom such as a fluorine atom,
chlorine atom, bromine atom or iodine atom.
[0045] These X and Y may optionally be bonded to form a ring. Each
of a halogen atom, an alkyl group or an aralkyl group is
independently preferable as X and Y in the fore-mentioned general
formula (1), and chlorine atom, methyl group or benzyl group is
more preferable.
[0046] Respective R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5,
R.sup.6, R.sup.7 and R.sup.8 in the fore-mentioned general formula
(1) independently represent a hydrogen atom, an alkyl group, an
aryl group, an aralkyl group, an alkoxy group, an aryloxy group, an
aralkyloxy group, a di-substituted amino group or a substituted
silyl group. Further, R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5,
R.sup.6, R.sup.7 and R.sup.8 may optionally be bonded to form a
ring. Each of an alkyl group, an aryl group, an aralkyl group, an
alkoxy group, an aryloxy group, an aralkyloxy group, a
di-substituted amino group or a substituted silyl group in R.sup.1,
R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7 or R.sup.8 is
similar as in X or Y.
[0047] An aryl group or a substituted silyl group is preferable as
R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7 or
R.sup.8 in the present invention.
[0048] In the fore-mentioned general formula (1), T represents a
divalent covalent cross-linking group having 1 to 20 carbon atoms,
or a divalent group represented by --O--, --S--, --S--S--,
--S(.dbd.O)--, --S(.dbd.O).sub.2--, --C(.dbd.O)--, --N(R.sup.9)--,
--P(R.sup.9)--, or --P(.dbd.O)(R.sup.9)-- (wherein R.sup.9
represents a hydrogen atom or a hydrocarbon group having 1 to 6
carbon atoms in each case) and n is an integer selected from 0 to
3.)
[0049] As the divalent common cross-linking group having 1 to 20
carbon atoms, methylene group, ethylene group, trimethylene group,
propylene group, diphenylethylene group, ethylidene group,
propylidene group, isopropylidene group, n-butylidene group,
isobutylidene group and the like are exemplified. Among them,
methylene group, ethylene group, ethylidene group, isopropylidene
group, or isobutylidene group is preferably used.
[0050] Further, in the divalent group represented by
--N(R.sup.9)--, --P(R.sup.9)--, or --P(.dbd.O)(R.sup.9)-- as T,
R.sup.9 represents a hydrogen atom or a hydrocarbon group having 1
to 24 carbon atoms in each case. As the hydrocarbon group, an alkyl
group having 1 to 24 carbon atoms, an aryl group having 6 to 24
carbon atoms or an aralkyl group having 7 to 24 carbon atoms is
preferable. An alkyl group having 1 to 24 carbon atoms is more
preferable.
[0051] A divalent group represented by --O-- or --S-- is preferable
as T, and --S-- is more preferable.
[0052] n is an integer of 0 to 3, and represents the number of the
unit T . Among these, 0 or 1 gives a preferable result in
particular, and n is more preferably 1.
[0053] The transition metal compound in the fore-mentioned general
formula (1) can be easily produced and isolated. For example, the
production process (I) and (II) described below are
illustrated.
[0054] (I) A process for producing the transition compound by
reacting a compound represented by the general formula (2)
described below with a transition metal compound represented by the
general formula (3) described below.
[0055] (II) A process for producing the transition compound by
reacting a compound of the general formula (2) described below with
an organoalkaline metal compound, an alkaline metal hydride
compound or an organomagnesium compound (hereinafter, sometimes
referred to as "the metal compound") to obtain a halide compound
and then reacting it with the transition metal compound represented
by the general formula (3) described below.
[0056] The halide compound may not be separated in the process
(II). Further, it is also possible in the process (II) to mix
together the compound represented by the general formula (2), the
metal compound and the transition metal compound represented by the
general formula (3) and react them. 2
[0057] (Wherein respective R.sup.1, R.sup.2, R.sup.3, R.sup.4,
R.sup.5, R.sup.6, R.sup.7 and R.sup.8 independently represent a
hydrogen atom, an alkyl group, an aryl group, an aralkyl group, an
alkoxy group, an aryloxy group, an aralkyloxy group, a
di-substituted amino group or a substituted silyl group, R.sup.1,
R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7 and R.sup.8
may arbitrarily bond to form a ring, T represents a divalent
covalent cross-linking group having 1 to 20 carbon atoms, or a
divalent group represented by --O--, --S--, --S--S--,
--S(.dbd.O)--, --S(.dbd.O).sub.2--, --C(.dbd.O)--, --N(R.sup.9)--,
--P(R.sup.9)--, or --P(.dbd.O)(R.sup.9)-- (wherein R.sup.9
represents a hydrogen atom or a hydrocarbon group having 1 to 6
carbon atoms in each case), and n is an integer of 0 to 3.)
MZ.sup.1Z.sup.2Z.sup.3Z.sup.4 (3)
[0058] (wherein M represents a transition metal atom of the Fourth
Group of the Periodic Table, and respective Z.sup.1, Z.sup.2,
Z.sup.3 and Z.sup.4 independently represent a halogen atom, an
alkoxy group, an aryloxy group, an aralkyloxy group, a
di-substituted amino group, an alkyl group, an aryl group or an
aralkyl group.)
[0059] Respective R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5,
R.sup.6, R.sup.7, R.sup.8 and T in the general formula (2) are the
same as in the general formula (1).
[0060] As specific examples of the compound represented by the
general formula (2), 2-(2-hydroxypropyl)phenol, cathecol,
resorcinol, 4-isopropylcathecol, 3-methoxycathecol,
1,8-dinydroxynaphthalene, 1,2-dinydroxynaphthalene,
2,2'-biphenyldiol, 1,1'-bi-2-naphthol,
2,2'-dihydroxy-6,6'-dimethylbiphenyl,
4,4',6,6'-tetra-tert-butyl-2,2'-met- hylenediphenol,
4,4',6,6'-tetramethyl-2,2'-isobutylidenediphenol,
2,2'-thiobis(4-methyl-6-isopropylphenol),
2,2'-thiobis(4,6-dimethylphenol- ),
2,2'-thiobis(4-methyl-6-tert-butyl)phenol and the like can be
exemplified. Among these, 2,4-dihydroxypentane, cathecol,
2,2'-biphenyldiol, 1,1'-bi-2-naphthol,
4,4',6,6'-tetra-tert-butyl-2,2'-me- thylenediphenol,
4,4'-dimethyl-6,6'-di-tert-butyl-2,2'-methylenediphenol,
4,4',6,6'-tetramethyl-2,2'-isobutylidenediphenol,
2,2'-thiobis(4-methyl-6- -isopropyl)phenol),
2,2'-thiobis(4,6-dimethylphenol) and
2,2'-thiobis(4-methyl-6-tert-butyl)phenol give a preferable
result.
[0061] In the transition metal compound represented by the
above-mentioned general formula (3), Z.sup.1, Z.sup.2, Z.sup.3 and
Z.sup.4 independently represent a halogen atom, an alkoxy group, an
aryloxy group, an aralkyloxy group, a sulfonyloxy group, a
di-substituted amino group, an alkyl group, an aryl group or an
aralkyl group. Further, these may be optionally bonded in part to
form a ring.
[0062] Z.sup.1, Z.sup.2, Z.sup.3 and Z.sup.4 are the same as in X
or Y in the above-mentioned general formula (1). More specific
examples of the transition metal compound represented by the
general formula (3) include titanium halides such as titanium
tetrachloride, titanium tetrabromide, titanium tetraiodide and the
like, titanium amides such as tetrakis(dimethylamino) titanium,
dichlorobis(dimethylamino) titanium, trichloro(dimethylamino)
titanium, tetrakis(diethylamino) titanium and the like,
alkoxytitaniums such as tetraisopropoxytitanium, tetra
n-butoxytitanium, diisopropoxytitanium dichloride,
isopropoxytitanium trichloride and the like, and compounds in which
titanium in the above-mentioned compounds is replaced with
zirconium or hafnium, etc.
[0063] In the production process (I) or (II), the amount used of
the transition metal compound represented by the general formula
(3) is usually 0.5 to 3-fold mol, and preferably 0.7 to 1.5-fold
mol based on the compound represented by the general formula
(2).
[0064] Specific examples of the organoalkaline metal compound used
in the production process (II) include organolithium compounds such
as methyllithium, ethyllithium, n-butyllithium, sec-butyllithium,
tert-butyllithium, lithium trimethylenesilyl acetylide, lithium
acetylide, trimethylsilyl methyllithium, vinyllithium,
phenyllithium, allyllithium and the like, organoalkaline metal
compounds in which lithium in these compounds is replaced with
sodium, potassium, rubidium or cesium. Preferably, an alkaline
metal compound having an alkyl group with 1 to 10 carbon atoms is
preferred, a compound having an alkyl group with 1 to 10 carbon
atoms of lithium, sodium or potassium is more preferred, and an
alkyllithium compound having an alkyl group with 1 to 10 carbon is
most preferred.
[0065] The alkaline metal hydride is a hydride of lithium, sodium,
potassium, rubidium or cesium, and sodium hydride or potassium
hydride is preferred.
[0066] Examples of the organomagnesium compound include
dialkylmagnesium compounds and alkylmagnesium halides, and
specifically, dimethylmagnesium, diethylmagnesium,
di-n-butylmagnesium, diisopropylmagnesium, n-butylethylmagnesium,
methylmagnesium iodide, methylmagnesium chloride,
isopropylmagnesium halide and the like. Alkylmagnesium halides
having an alkyl group of 1 to 10 carbon atoms are preferred.
[0067] As the above-mentioned metal compounds, organoalkaline metal
compounds or alkaline metal hydrides are preferable and the
alkyllithium is more preferable. The amount used of the metal
compound in the production process (II) is usually 1 to 5-fold mol
based on the compound represented by the general formula (2).
[0068] The reaction is generally carried out in the presence of a
solvent. Examples of the solvent used include an aprotic solvent of
an aromatic hydrocarbon such as benzene, toluene, xylene,
mesitylene or the like, an aliphatic hydrocarbon such as pentane,
hexane, heptane, octane or the like, an ether type solvent such as
diethyl ether, tetrahydrofuran, 1,4-dioxane or the like, an amide
type solvent such as hexamethylphosphoric amide, dimethyl amide, a
polar solvent such as acetonitrile, propionitrile, acetone, diethyl
ketone, methylisobutyl ketone, cyclohexanone or the like, a
halogenated solvent such as dichloromethane, dichloroethane,
chlorobenzene, dichlorobenzene, or the like, etc. Such solvent is
used alone or two or more in combination, and the amount used
thereof is usually 1 to 200 ml/g based on the volume to weight of
the compound represented by the general formula (2) and Preferably
3 to 50 ml/g.
[0069] The reaction (I) can be carried out in the presence of a
tertiaryamine compound or the like, and triethylamine and
diisopropylethylamine, N,N,N',N'-tetramethylethylenediamine and the
like are preferably used as the tertiaryamine compound as an
additive aid. The amount used is 1 to 10-fold mol based a compound
represented by the general formula (2), preferably 1.5 to 5-fold
mol and more preferably 1.8 to 4-fold mol.
[0070] The reaction of the production process (I) is carried out in
a range of -100.degree. C. to 200.degree. C., and preferably
-80.degree. C. to 150.degree. C. A range of -50.degree. C. to
120.degree. C. is more preferable. The reaction temperature in the
production process (II) is usually from -100.degree. C. to the
boiling point of the solvent used as a medium, but when the
organoalkaline metal is used, a range of -80.degree. C. to
40.degree. C. is preferable and when the organomagnesium compound
is used, a range of 10.degree. C. to 100.degree. C. is preferable,
respectively.
[0071] When there is a solid component which is produced as a
by-product by the reaction from the reaction mixture containing the
transition metal compound represented by the general formula (I)
according to the above-mentioned reaction, it is separated by
filtration or the like in the presence of a predetermined solvent,
and further, after heating and concentrating the solvent or by
standing alone in another solvent alone or a mixed solvent at a
cooled dark place, crystals of the complex can be separated.
Further, it is possible to efficiently precipitate the desired
complex in high purity to take out, while industrially stirring
without standing alone, for example, cooling gradually.
[0072] The compound represented by the general formula (2) in the
present invention is produced by various processes. For example,
when T is a sulfur atom, the compound can be easily synthesized by
reacting various kind of phenol compounds with sulfur dichloride in
a solvent while stirring.
[0073] The solvent used includes an aprotic solvent of an aliphatic
hydrocarbon such as pentane, hexane, heptane, octane or the like,
an etheral solvent such as diethyl ether, tetrahydrofuran,
1,4-dioxane or the like, a halogenated hydrocarbon solvent such as
dichloromethane, dichloroethane, chlorobenzene, dichlorobenzene or
the like, etc.
[0074] The component (B) in the above-mentioned olefin
polymerization catalyst is an organoaluminumoxy compound soluble in
an aromatic hydrocarbon solvent. The examples thereof include
methylaluminoxane, ethylaluminoxane, propylaluminoxane,
butylaluminoxane, isobutylaluminoxane, methylethylaluminoxane,
methylbutylaluminoxane, methylisobutylaluminoxane, the
organoaluminumoxy compound represented by the general formula (4)
or (5) described below, and the like. Among them,
methylisobutylaluminoxane, and the organoaluminumoxy compounds
represented by the general formula (4) and (5) described below are
preferred. 3
[0075] (wherein R represents methyl group or isobutyl group, the
presence ratio of a methyl group and an isobutyl group is methyl
group: isobutyl group=5 to 95:95 to 5. m represents a number in a
range of 1 to 50.)
[0076] The organoaluminumoxy compound soluble in an aromatic
hydrocarbon solvent which is used in the present invention can form
a component insoluble in the aromatic hydrocarbon solvent by
reacting with water.
[0077] The amount of the organoaluminumoxy compound used can be
usually selected in a wide range of 1 to 20,000 mol in terms of an
aluminum atom contained in the organoaluminumoxy compound per one
mol of a transition metal atom contained in the transition metal
compound (A). The preferable range is from 100 to 10,000 mol per
one mol of the transition metal atom.
[0078] Water is used as the component (C) in the above-mentioned
olefin polymerization catalyst. The amount of the water (C) used
can be usually selected in a wide range of 0.1 to 3.0 mol per one
mol of an aluminum atom contained in the organoaluminumoxy compound
(B). The preferable range is from 0.1 to 1.0 per one mol of the
aluminum atom.
[0079] As a method of feeding the respective catalyst components in
a polymerization reactor, a transition metal compound (A), an
aromatic organoaluminumoxy compound (B) and water (C) may be
separately fed or may be fed after contacting them in advance.
[0080] Specific examples of a method of previously contacting
include a method of contacting an organoaluminumoxy compound (B)
with water (C) and then removing the solvent followed by contacting
with the component (A), a method of contacting the component (B)
with the component (C) and then contacting with the component (A),
a method of contacting the component (A), the component (B) and the
component (C) at the same time, and the like. Examples of a
contacting method of the component (C) include a method of directly
contacting water, a method of previously mixing water with a
solvent and contacting the mixture with other components, a method
of contacting a metal salt containing a crystal water or an
inorganic or organic material containing absorbed water with other
components, a method of contacting a gas such as nitrogen
containing moisture, or the like with other components, etc. when
the component (B) is contacted with the component (C), a component
insoluble in an aromatic hydrocarbon solvent sometimes form.
[0081] Polymerization is usually carried out over a wide range of
-30 to 300.degree. C., preferably 0 to 280.degree. C. and more
preferably 20 to 250.degree. C.
[0082] The polymerization pressure is not particularly restricted,
and is preferably from about normal pressure to about 150 atom from
industrial and economic viewpoints. The polymerization time is
suitably determined according to a kind of the desired polymer and
a reaction apparatus in general, and adopts a range of 30 seconds
to 40 hours.
[0083] As a polymerization process, either of batch type and
continuous type are applicable. Further, a slurry or solution
polymerization with an inert hydrocarbon solvent such as propane,
pentane, hexane, heptane, octane or the like, a bulk polymerization
using a monomer as a solvent or a gas phase polymerization is
applicable.
[0084] A chain transfer agent such as hydrogen or the like can be
added in order to control the molecular weight of the olefin
polymer.
EXAMPLE
[0085] The present invention is specifically illustrated according
to Examples below, but the scope of the present invention is not
restricted by Examples.
[0086] The value of respective items in Examples was measured by
methods described below.
[0087] (1) Polystyrene-Reduced Weight Average Molecular Weight
(Mw), Polystyrene-Reduced Number Average Molecular Weight (Mn) and
Molecular Weight Distribution (Mw/Mn)
[0088] They were measured with a gel permeation chromatograph (GPC)
under conditions described below. A calibration curve was prepared
using a standard polystyrene.
[0089] Measuring instrument: 150 CV type manufactured by Millipore
Waters Company Ltd.
[0090] Column: Shodex M/S 80
[0091] Measurement temperature: 145.degree. C.,
[0092] Solvent: Ortho-dichlorobenzene
[0093] Sample concentration: 5 mg/8 ml
[0094] (2) Measurement with a Differential Scanning Calorimeter
(DSC)
[0095] It was measured under the conditions below using DSC-VII
manufactured by Perkin-Elmer Company, Ltd.
[0096] Raising temperature: 20.degree. C. to 200.degree. C.
(20.degree. C/min.), retention for 10 min.
[0097] Cooling: 200.degree. C. to -100.degree. C. (20.degree.
C/min.), retention for 10 min.
[0098] Measurement: -100.degree. C. to 300.degree. C. (raising
temperature at 20.degree. C./min.)
Reference Example 1
[0099] Synthesis of
Dichloro{2,2'-thiobis[4-methyl-6-(tert-butyl)phenolato- ]}
Titanium
[0100] The title compound was synthesized according to a literature
(Arjan van der Linden et. al., Journal of the American Chemical
Society, 117, 3008(1995)) 4
Example 1
[0101] An egg-plant type flask with an inner volume of 300 ml was
replaced with argon, 20 mmol of (poly)methylisobutyl aluminoxane
(hereinafter, sometimes abbreviated to as "MMAO") manufactured by
Tosoh-Akzo Co., Ltd. of toluene solution and 11 mmol of water were
added therein and the mixture was mixed by stirring for 10
minutes.
[0102] On the other hand, in an egg-plant type flask with an inner
volume of 25 ml replaced with argon, 5 ml of purified toluene and
1.2 mg of dichloro{2,2'-thiobis[4-methyl-6-(tert-butyl)phenolato}
titanium were mixed by stirring, and then charged into the
above-mentioned egg-plant type flask. The molar ratio of [Al]/[Ti]
of the catalyst solution prepared then was 8,000. After the
catalyst solution was mixed by stirring at room temperature for 10
minutes, 63 ml of 1-hexene was charged and the polymerization was
carried out at 40.degree. C. for 3 minutes. After completion of the
polymerization, the contents in the flask were charged into about
400 ml of an acidic methanol, and the precipitated polymer was
filtered to be dried at 80.degree. C. for about 2 hours. As a
result, 0.63 g of poly(1-hexene) copolymer was obtained. Mw of the
polymer obtained was 566.times.10.sup.4, Mn was 297.times.10.sup.4,
Mw/Mn was 1.9, no crystal fusion peak by DSC was detected, and the
polymer was amorphous. The glass transition temperature was
observed at -46.degree. C.
Example 2
[0103] An egg-plant type flask with an inner volume of 100 ml was
replaced with argon, 20 mmol of MMAO and 11 mmol of water were
added therein and the mixture was mixed by stirring for 10
minutes.
[0104] On the other hand, in an egg-plant type flask with an inner
volume of 25 ml replaced with argon, 5 ml of purified toluene and
1.2 mg of dichloro{2,2'-thiobis[4-methyl-6-(tert-butyl)phenolato}
titanium were mixed by stirring, and then charged into the
above-mentioned egg-plant type flask of 100 ml. The molar ratio of
[Al]/[Ti] of the catalyst solution prepared then was 8,000. After
the catalyst solution was mixed by stirring at room temperature for
10 minutes, 31.2 ml of 1-octene was charged and the polymerization
was carried out at 40.degree. C. for 10 minutes. After completion
of the polymerization, the contents of the flask were charged into
about 400 ml of an acidic methanol, and the precipitated polymer
was filtered to be dried at 80.degree. C. for about 2 hours. As a
result, 0.12 g of poly(1-octene) copolymer was obtained. Mw of the
polymer obtained was 599.times.10.sup.4, Mn was 294.times.10.sup.4,
Mw/Mn was 2.0, no crystal fusion peak by DSC was detected, and the
polymer was amorphous. The glass transition temperature was
observed at -61.degree. C.
Comparative Example 1
[0105] An egg-plant type flask with an inner volume of 50 ml was
replaced with argon, and 1 mmol of MMAO was added therein.
[0106] On the other hand, in an egg-plant type flask with an inner
volume of 25 ml replaced with argon, 2 ml of purified toluene and
4.8 mg of dichloro{2,2'-thiobis[4-methyl-6-(tert-butyl)phenolato}
titanium were mixed by stirring, and then charged into the
above-mentioned egg-plant type flask of 50 ml. The molar ratio of
[Al]/[Ti] of the catalyst solution prepared then was 100. After the
catalyst solution was mixed by stirring at room temperature for 10
minutes, 6.3 ml of 1-hexene was charged and the polymerization was
carried out at 40.degree. C. for 1 hour. After completion of the
polymerization, the contents of the flask were charged into about
400 ml of an acidic methanol, and the precipitated polymer was
filtered to be dried at 80.degree. C. for about 2 hours. As a
result, 0.31 g of poly(1-hexene) was obtained. Mw of poly(1-hexene)
obtained was 20.times.10.sup.4 Mn was 8.times.10.sup.4, Mw/Mn was
2.5.
[0107] As described above, according to the present invention, an
amorphous polymer having a high molecular weight enough to improve
problems such as stickiness and elution to an organic solvent and
to exhibit an elastomeric property, and substantially not having a
melting point, and a process for producing the amorphous polymer,
are provided.
* * * * *