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The present invention relates to novel polymers obtained by the
polymerization of substituted 1,3-butadiene compounds, and a process for
their preparation. More particularly, the present invention relates to
polydienes having reactive silyl groups and a process for their
preparation. Conventional reactive silane compounds are, in many cases,
intended for surface treatment of inorganic substances, and they are, in
most cases, low molecular weight compounds. Further, polymerizable silane
compounds such as vinyl compounds or methacrylate compounds having
reactive silyl groups are known. However, such polymerizable silane
compounds are intended for use in a small amount for the copolymerization
with other plastic materials, and they have not usually used alone for
polymerization.
The present inventors have found that polymers having reactive silyl groups
and carbon-carbon double bonds which are not found in the conventional
silane compounds, can be used for various applications. The present
invention is based on this discovery.
The present invention provides a polymer obtained by the polymerization of
a substituted 1,3-butadiene compound of the formula:
##STR2##
wherein each of X.sub.1 and X.sub.2 is hydrogen or SiR.sub.1 R.sub.2
R.sub.3, provided that at least one of X.sub.1 and X.sub.2 is SiR.sub.1
R.sub.2 R.sub.3, wherein each of R.sub.1, R.sub.2 and R.sub.3 is halogen,
lower alkyl or lower alkoxy, provided that R.sub.1, R.sub.2 and R.sub.3
are not lower alkyl at the same time.
Most of the polymer structure of the present invention has a unit of the
formula:
##STR3##
wherein X.sub.1 and X.sub.2 are as defined above.
Now, the present invention will be described in detail with reference to
the preferred embodiments.
By virtue of the reactive silyl groups and carbon-carbon double bonds, the
homopolymer of the present invention is useful for an improvement of the
impact resistance of plastics by imparting rubber elasticity to the
surface of an inorganic filler, for the production of highly oriented
magnetic substance by imparting rubber elasticity to the surface of
magnetic substance, and for blending with a rubber, followed by
co-vulcanization, or it is useful for the cross-linking by means of the
reactive silyl groups, for an improvement of the hydrolysis resistance of
e.g. FRP (fiber reinforced plastics) by the treatment of the surface of an
inorganic filler and for applications to e.g. adhesives for glass,
ceramics or rubber products. Further, it may be used for various other
purposes.
In some cases, the monomer of the substituted 1,3-butadiene compound may be
added to the above material, and then polymerized.
The copolymer of the present invention is likewise useful for an
improvement of the heat resistance of plastics, for adhesives for glass,
ceramics or rubber products, and for coupling agents, since it is readily
crosslinkable by virtue of the reactive silyl groups and carbon-carbon
double bonds, and it is further useful for various other applications.
The homopolymers and copolymers of the present invention may further be
useful as anionic polymeric initiators to produce polymers having affinity
with inorganic substances.
Among them, living polymers are particularly useful as anionic polymeric
initiators, for instance, for the preparation of living block copolymers.
The polymers obtainable by these living polymers are useful for an
improvement of the impact resistance of plastics by imparting rubber
elasticity to the surface of inorganic fillers, for the production of
highly dispersible magnetic material by coating the surface of the
magnetic substance, and for blending with rubber, followed by
co-vulcanization, by virtue of the reactive silyl groups and carbon-carbon
double bonds. Further, they are useful for cross linking by means of the
reactive silyl groups, for an improvement of the hydrolysis resistance of
e.g. FRP by the treatment of the surface of inorganic fillers, and for
adhesives for glass, ceramics or rubber products. They are further useful
for various other applications such as for UV photo-resists.
Further, the living homopolymers of the present invention are useful as
starting materials for living block copolymers with other unsaturated
monomers such as styrene, .alpha.-methylstyrene, 1,3-butadiene, isoprene,
methyl acrylate, methyl methacrylate, acrylonitrile and methacrylonitrile,
and for block copolymers obtained therefrom. They are useful as
compatibility improvers for a blend with other polymers, for medical
purposes by virtue of the microphase separation structures, and as impact
resistance improvers.
The novel polydiene having reactive silyl groups of the present invention
are obtained by subjecting the substituted 1,3-butadiene compound of the
formula I to homopolymerization or to copolymerization with an unsaturated
monomer.
The substituted 1,3-butadiene compound to be used for the polymerization of
the present invention includes 1-trimethoxysilyl-1,3-butadiene,
1-triethoxysilyl-1,3-butadiene, 1-triisopropoxysilyl-1,3-butadiene,
1-tri-n-propoxysilyl-1,3-butadiene, 1-methoxydimethylsilyl-1,3-butadiene,
1-dimethoxymethylsilyl-1,3-butadiene, 1-trichlorosilyl-1,3-butadiene and
1-dimethylchlorosilyl-1,3-butadiene.
Further, 2-trimethoxysilyl-1,3-butadiene, 2-triethoxysilyl-1,3-butadiene,
2-triisopropoxysilyl-1,3-butadiene, 2-tri-n-propoxysilyl-1,3-butadiene,
2-methoxydimethylsilyl-1,3-butadiene,
2-dimethoxymethylsilyl-1,3-butadiene, 2-trichlorosilyl-1,3-butadiene and
2-dimethylchlorosilyl-1,3-butadiene may also be employed.
Further, the novel copolymers having reactive silyl groups and
carbon-carbon double bonds of the present invention can be obtained also
by copolymerizing the substituted 1,3-butadiene compound of the formula I
with one or more unsaturated monomers.
Such unsaturated monomers to be used in the present invention include
unsaturated hydrocarbons such as ethylene, propylene, acetylene, styrene
and .alpha.-methylstyrene, vinyl compounds such as vinyl acetate, vinyl
chloride, acrylonitrile and methacrylonitrile, acrylic or methacrylic
esters such as ethyl acrylate, 2-ethylhexyl acrylate, methyl methacrylate
and n-butyl methacrylate, diene compounds such as isoprene, chloroprene
and butadiene, maleic acid derivatives such as maleic anhydride and
di-2-ethylhexyl maleate, and unsaturated carboxylic acids such as acrylic
acid, methacrylic acid and itaconic acid.
There is no particular restriction as to the molecular weights of the
homopolymers and copolymers of the present invention, which may be
polymers or oligomers. Likewise, there is no particular restriction as to
the proportions of the copolymer constituents.
Any of radical polymerization, cationic polymerization and anionic
polymerization may be employed for the process for the preparation of the
polymer of the present invention.
The radical polymerization may be initiated by application of high
temperature heating and radiation or by means of an initiator. The
initiator includes an azo initiator such as 2,2'-azobisisobutyronitrile, a
peroxide initiator such as benzoylperoxide, and a redox initiator composed
of a combination of benzoylperoxide and N,N-dimethylaniline.
As initiators for the cationic polymerization, Lewis acid initiators such
as aluminum chloride, boron trifluoride and dichloromonoethylaluminum may
be mentioned.
As initiators for the anionic polymerization, alkyl metals such as
naphthalene sodium and n-butyl lithium, and Ziegler type catalysts may be
mentioned.
In particular, the living polymerization initiators for the present
invention include lithium naphthalide, sodium naphthalide, potassium
naphthalide, oligo-.alpha.-methylstyryl lithium,
oligo-.alpha.-methylstyryl sodium, oligo-.alpha.-methylstyryl potassium,
cumyl potassium and n-butyl lithium.
However, by mere high temperature heating, the degree of polymerization of
the homopolymer was rather low. Further, with an initiator having a low
activity such as 2,2-azobisisobutyronitrile, the yield of a copolymer with
a maleic acid derivative was rather low.
The above polymerization reactions may be conducted by directly adding the
initiator to the substituted 1,3-butadiene compound or to a mixture of the
substituted 1,3-butadiene compound with an unsaturated monomer, or may be
conducted in a solvent which does not adversely affect the polymerization
reaction.
With respect to such a solvent, the radical polymerization may be conducted
in a solvent which is commonly used in a usual solution polymerization,
such as toluene or ethyl acetate, and the cationic polymerization may
preferably conducted in a halogenated hydrocarbon such as carbon
tetrachloride, chloroform or methylene chloride.
Further, for the anionic polymerization, benzene, toluene, hexane,
cyclohexane, preferably ether-type solvent such as tetrahydrofuran or
dioxane may be used.
The radical polymerization is conducted at a temperature of from
-100.degree. to 100.degree. C., from 1 to 100 hours, preferably in the
presence of a solvent.
The cationic polymerization is conducted at a low temperature of from
-100.degree. C. to room temperature, for 1 to 100 hours, preferably in the
presence of a solvent.
The anionic polymerization is conducted at a low temperature of from
-100.degree. C. to room temperature, for from 0.1 to 100 hours, preferably
in the presence of a solvent. The anionic polymerization reaction is
conducted in an inert gas atmosphere in the absence of moisture or oxygen
which adversely affects the polymerization reaction.
The weight-average molecular weight of the polymers obtained by radical
polymerization was from about 500 to about 2,000,000.
The weight-average molecular weight of the polymers obtained by the
cationic polymerization was from about 500 to about 10,000.
Likewise, the weight-average molecular weight of the polymers obtained by
the anionic polymerization was from about 500 to about 500,000.
The molecular weight of a living polymer can be controlled by adjusting the
ratio of the substituted 1,3-butadiene compound to the anionic
polymerization initiator. Namely, it is possible to increase the molecular
weight by increasing the ratio.
The living polymers thus obtained usually have a weight-average molecular
weight of from about 500 to about 500,000, preferably from about 2,000 to
about 200,000, more preferably from about 5,000 to about 100,000, in view
of the physical properties of the polymers obtainable from the living
polymers.
The living polymers and the polymers obtainable from the living polymers,
are polymers having extremely narrow molecular weight distribution with
the ratio of the weight-average molecular weight to the number-average
molecular weight being close to 1.
Now, the present invention will be described in further detail with
reference to Examples. However, it should be understood that the present
invention is by no means restricted to these specific Examples.
EXAMPLE 1
Into a glass ampoule, 5.22 g (3.times.10.sup.-2 mol) of distilled
2-trimethoxysilyl-1,3-butadiene and 0.03 g (1.8.times.10.sup.-4 mol) of
azoisobutyronitrile were introduced, and the ampoule was sealed and
immersed in a constant-temperature water bath of 60.degree. C., whereupon
the reaction was conducted for 10 hours.
After the reaction, the reaction mixture was taken out from the ampoule and
subjected to vacuum drying to obtain a polymer.
The polymer thus obtained was dissolved in tetrahydrofuran and subjected to
gel permeation chromatography for the measurement of the molecular weight,
whereby the weight-average molecular weight was found to be 5,200.
Further, the glass transition temperature was measured by differential
scanning calorimeter (DSC) at a rate of heating of 10.degree. C./min,
whereby it was found to be -43.degree. C.
EXAMPLE 2
300 g (1.72 mol) of 2-trimethoxysilyl-1,3-butadiene and 6 g
(2.0.times.10.sup.-2 mol) of
1,1-di-t-butylperoxy-3,3,5-trimethylcyclohexane (Trigonox 29, manufactured
by Kayaku Noury K.K.) were charged into a flask, and the flask was dipped
in a constant-temperature water bath of 105.degree. C., whereby the
reaction was conducted for 2.5 hours. The rest of treatment was conducted
in the same manner as in Example 1.
The yield of the polymer obtained was 80%, and the weight-average molecular
weight was 129,000.
The microstructure of this poly(2-trimethoxysilyl-1,3-butadiene) was a
1,4-addition type and was composed of 70% of the cis-form and 30% of the
trans-form. The glass transition temperature was -43.degree. C.
EXAMPLE 3
100 g (5.75.times.10.sup.-1 mol) of 2-trimethoxysilyl-1,3butadiene and 2 g
(1.25.times.10.sup.-2 mol) of t-butyl peroxy-isobutyrate (Kayaester I,
manufactured by Kayaku Noury K.K.) were charged into a flask, and the
flask was dipped in a constant-temperature water bath of 90.degree. C.,
whereupon the reaction was conducted for 3 hours and 40 minutes. The rest
of treatment was conducted in the same manner as in Example 1.
The yield of the polymer thus obtained was 85%, and the weight-average
molecular weight was 32,000.
EXAMPLE 4
The polymerization reaction and treatment were conducted in the same manner
as in Example 1 except that 5.22 g (3.times.10.sup.-2 mol) of
2-trimethoxysilyl-1,3-butadiene, 2 ml of ethyl acetate, 0.1 g
(4.1.times.10.sup.-4 mol) of benzoyl peroxide and 0.1 g
(8.3.times.10.sup.-4 mol) of N,N-dimethylaniline were reacted for 24
hours.
The weight-average molecular weight of the polymer thus obtained was
95,000.
The glass transition temperature was -43.degree. C.
EXAMPLE 5
The polymerization reaction and treatment were conducted in the same manner
as in Example 1 except that 5.22 g (3.times.10.sup.-2 mol) of
2-trimethoxysilyl-1,3-butadiene, and 0.05 g (3.5.times.10.sup.4 mol) of
boron trifluoride-diethyl ether adducts were reacted for 1.6 hours.
The weight-average molecular weight of the polymer thus obtained was 2,700.
EXAMPLE 6
Into a glass ampoule, 2.61 g (1.5.times.10.sup.-2 mol) of distilled
2-trimethoxysilyl-1,3-butadiene, 1.50 g (1.5.times.10.sup.-2 mol) of
methyl methacrylate and 0.1 g (4.times.10.sup.-4 mol) of
2,2-azobis(2,2-dimethylvaleronitrile) (V-65, manufactured by Wako Junyaku
K.K.) were introduced, and the ampoule was sealed and dipped in a
constant-temperature water bath of 60.degree. C., whereupon the reaction
was conducted for 24 hours.
After the reaction, the reaction mixture was taken out from the ampoule and
subjected to precipitation with anhydrous methanol. The copolymer thus
obtained was vacuum-dried.
The yield of the copolymer thus obtained was 82%. From the results of the
elementary analysis, the copolymer was found to comprise 6.0% of silicon,
55.6% of carbon, 8.02% of hydrogen, the rest being oxygen, and the
2-trimethoxysilyl-1,3-butadiene component was about 37% by weight.
Further, the copolymer was dissolved in tetrahydrofuran and subjected to
gel permeation chromatography for the measurement of the molecular weight,
whereby the weight-average molecular weight was found to be 12,000.
EXAMPLE 7
The polymerization reaction and treatment were conducted in the same manner
as in Example 6 except that 2.61 g (1.5.times.10.sup.-2 mol) of
2-trimethoxysilyl-1,3-butadiene, 1.47 g (1.5.times.10.sup.-2 mol) of
maleic anhydride, 2 ml of ethyl acetate and 0.1 g (6.1.times.10.sup.-4
mol) of 2,2-azobisisobutyronitrile were reacted for 24 hours.
The yield was 7%, and the 2-trimethoxysilyl-1,3-butadiene component was
about 48%.
The weight-average molecular weight of the polymer thus obtained was
55,000.
EXAMPLE 8
The reaction and treatment were conducted in the same manner as in Example
6 except that 2.61 g (1.5.times.10.sup.-2 mol) of
2-trimethoxysilyl-1,3-butadiene, 1.56 g (1.5.times.10.sup.-2 mol) of
styrene, 0.1 g (4.1.times.10.sup.-4 mol) of benzoyl peroxide and 0.1 g
(8.3.times.10.sup.-4 mol) of N,N-dimethylaniline were reacted at
100.degree. C. for 10 hours.
The yield was 33%, and the 2-trimethoxysilyl-1,3butadiene component was
about 19%.
The weight-average molecular weight of the polymer thus obtained was
51,000.
EXAMPLE 9
The reaction and treatment were conducted in the same manner as in Example
6 except that 2.61 g (1.5.times.10.sup.-2 mol) of
2-trimethoxysilyl-1,3-butadiene, 1.50 g (1.5.times.10.sup.-2 mol) of
methyl methacrylate, 2 ml of toluene, 0.1 g (4.1.times.10.sup.-4 mol) of
benzoyl peroxide and 0.1 g (8.3.times.10.sup.-4 mol) of
N,N-dimethylaniline were reacted for 24 hours.
The yield was 65%, and the 2-trimethoxysilyl-1,3butadiene component was
about 18%.
The weight average molecular weight of the polymer thus obtained was
73,000.
EXAMPLE 10
Anionic polymerization was conducted in the following manner by using an
apparatus comprising a reaction flask connected to a highly vacuumed line
and breakably sealed ampoules in which a solution mixture comprising
3.88.times.10.sup.-3 mol of 2-triisopropoxysilyl-1,3-butadiene and 5 ml of
tetrahydrofuran, a solution mixture comprising 2.38.times.10.sup.-4 mol of
.alpha.-methylstyrene and 5 ml of tetrahydrofuran, and 0.119 mmol of
potassium naphthalide were, respectively, freezed, degassed and sealed in.
Namely, into the reaction flask maintained at 10.sup.-6 mmHg for 5 hours
for degassing and cooled to -78.degree. C., potassium naphthalide cooled
to -78.degree. C. and the solution mixture comprising
.alpha.-methylstyrene and tetrahydrofuran were introduced by breaking the
seals of the respective ampoules. (Oligo-.alpha.-methylstyryl potassium
was obtained.)
Then, into the reaction flask, the tetrahydrofuran solution of
2-triisopropoxysilyl-1,3-butadiene was likewise introduced from the
ampoule containing the tetrahydrofuran solution of
2-triisopropoxysilyl-1,3-butadiene. Then, the reaction was conducted at
-78.degree. C. for 0.5 hour, at 0.degree. C. for 1.5 hours and further at
20.degree. C. for 1 hour. The polymerization system was colored yellow
brown specific to the living anion. This color disappeared immediately
upon an addition of a small amount of water or methanol.
This living polymer was mixed with water at room temperature, then
extracted with diethyl ether and dried over magnesium sulfate. Then,
diethyl ether was removed to obtain
poly(2-triisopropoxysilyl-1,3-butadiene) in a yield of 90%.
The glass transition temperature of this
poly(2-triisopropoxysilyl-1,3-butadiene) was -36.degree. C., and the
polymer was soluble in organic solvents such as ethanol, pyridine,
dioxane, tetrahydrofuran, benzene, chloroform and acetone.
Further, this poly(2-triisopropoxysilyl-1,3butadiene) was dissolved in
tetrahydrofuran and subjected to gel permeation chromatography based on
standard polystyrene, whereby the number-average molecular weight was
13,500. Whereas, the calculated value of the number-average molecular
weight was 17,400.
The ratio of the weight-average molecular weight to the number-average
molecular weight was 1.07.
The microstructure of this poly(2-triisopropoxysilyl-1,3-butadiene) was a
1,4-addition type and was composed of 100% cis-form.
EXAMPLE 11
The treatment was conducted in the same manner as in Example 10 except that
ampoules wherein a solution mixture of 3.81.times.10.sup.-3 mol of
2-triisopropoxysilyl-1,3-butadiene and 5 ml of tetrahydrofuran and a
solution mixture of 1.48.times.10.sup.-4 mol of lithium naphthalide and 5
ml of tetrahydrofuran were, respectively, freezed, degassed and sealed,
were used and the reaction was conducted at -78.degree. C. for 1 hour, at
0.degree. C. for 1 hour and at 20.degree. C. for 1 hour.
The polymerization system was colored yellow specific to the living anion.
However, the color disappeared immediately upon an addition of a small
amount of water or methanol.
The yield of poly(2-triisopropoxysilyl-1,3-butadiene) was 88%.
The polymer was soluble in organic solvents such as ethanol, pyridine,
dioxane, tetrahydrofuran, benzene, chloroform and acetone.
The number-average molecular weight was 15,500, and the calculated value
was 13,300.
The ratio of the weight-average molecular weight to the number-average
molecular weight was 1.15.
The microstructure of this poly(2-triisopropoxysilyl-1,3-butadiene) was a
1,4-addition type and composed of 100% cis-form.
EXAMPLE 12
The treatment was conducted in the same manner as in Example 10 except that
ampoules in which a solution mixture of 4.41.times.10.sup.-3 mol of
2-trimethoxysilyl-1,3-butadiene and 5 ml of tetrahydrofuran, a solution
mixture of 2.48.times.10.sup.-4 mol of .alpha.-methylstyrene and 5 ml of
tetrahydrofuran, and 1.24.times.10.sup.-4 mol of potassium naphthalide
were, respectively, freezed, degassed and sealed, were used.
The polymerization system was colored yellow brown specific to the living
anion. However, the color disappeared immediately upon an addition of a
small amount of water or methanol.
The yield of poly(2-trimethoxysilyl-1,3-butadiene) was 100%.
The glass transition temperature was -36.degree. C., and the polymer was
soluble in organic solvents such as ethanol, pyridine, dioxane,
tetrahydrofuran, benzene, chloroform and acetone.
The number-average molecular weight was 22,000, and the calculated value
was 13,400.
The ratio of the weight-average molecular weight to the number average
molecular weight was 1.25. The microstructure of this
poly(2-trimethoxysilyl-1,3-butadiene) was a 1,4-addition type and was
composed of 70% cis-form and 30% trans-form.
EXAMPLE 13
Anionic polymerization was conducted in the following manner by using an
apparatus comprising a reaction flask connected to a highly vacuumed line
and ampoules in which a solution mixture of 1.17.times.10.sup.-2 mol of
2-trimethoxysilyl-1,3-butadiene and 5 ml of tetrahydrofuran, a solution
mixture of 5.30.times.10.sup.-4 mol of .alpha.-methylstyrene and 5 ml of
tetrahydrofuran, a solution mixture of 3.29.times.10.sup.-2 mol of
isoprene and 5 ml of tetrahydrofuran, and 1.19.times.10.sup.-4 mol of
potassium naphthalide were, respectively, freezed, degassed and sealed.
Namely, the reaction flask was maintained at 10.sup.-6 mmHg for 5 hours for
degassing. The sealing of ampoules containing potassium naphthalide and
the solution mixture of .alpha.-methylstyrene and tetrahydrofuran was
broken, and the contents were introduced into the reaction flask at room
temperature. The color of the solution was red.
Then, after cooling the solution at -78.degree. C., the sealing of the
ampoule containing isoprene and tetrahydrofuran was broken, and the system
was maintained at -78.degree. C. for 3 hours. The color of the solution
was brown.
Then, the sealing of the ampoule containing 1.17.times.10.sup.-2 mol of
2-trimethoxysilyl-1,3-butadiene and 5 ml of tetrahydrofuran was broken,
and the reaction was conducted for 14 hours from 0.degree. C. to room
temperature.
The polymerization system was colored yellow brown specific to the living
anion. However, this color disappeared immediately upon an addition of a
small amount of water or methanol.
Then, this living block copolymer was treated in the same manner as in
Example 10 to obtain a block copolymer. Yield was 73%.
The block copolymer thus obtained was as follows:
--(A).sub.m (B).sub.n (A).sub.m
wherein A represents 2-trimethoxysilyl-1,3-butadiene and B represents
isoprene
Measured values: 2m=195, n=634
Calculated values: 2m =197, n=553
This copolymer undergoes cross linking to form --Si--O--Si linkages in an
acidic atmosphere and forms a crosslinked polymer which is insoluble and
scarcely swelled in benzene or tetrahydrofuran.
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Description |
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