Preparation method of a polypropylene and a polypropylene obtained therefrom

Abstract

The present invention relates to a preparation method of a polypropylene and a polypropylene obtained therefrom. More specifically, it relates to a method of preparing a polypropylene by using a catalyst that includes a novel metallocene compound having an excellent polymerization activity, and a polypropylene obtained by the method. According to the present invention, since the polypropylene is prepared by polymerizing propylene by using a novel metallocene compound having an excellent polymerization activity and hydrogen reactivity, the properties of the polypropylene can be easily controlled and the polypropylene having excellent mechanical properties can be obtained.

Claims

1. A method of preparing a polypropylene, including a step of polymerizing propylene in the presence of a catalyst including a metallocene compound represented by Chemical Formula 1, wherein the catalyst is a supported catalyst including the metallocene compound, an alkylaluminoxane cocatalyst, and a boron-based cocatalyst which are supported on a carrier: ##STR00006## in Chemical Formula 1, M.sup.1 is a group 3 transition metal, a group 4 transition metal, a group 5 transition metal, a lanthanide transition metal, or an actinide transition metal; X is, same to or different from each other, a halogen; A is a group 14 element bridging indenyl groups; R.sup.1 is a C.sub.1-C.sub.20 alkyl, alkenyl, alkylaryl, arylalkyl, or aryl; R.sup.2 is hydrogen, a C.sub.1-C.sub.20 alkyl, alkenyl, alkylaryl, arylalkyl, or aryl; R.sup.3, R.sup.3′, R.sup.4, and R.sup.4′ are, same to or different from each other, respectively a C.sub.1-C.sub.20 alkyl, alkenyl, alkylaryl, arylalkyl, or aryl; and n is an integer of 1 to 20.

2. The method of preparing a polypropylene according to claim 1, wherein R.sup.1 and R.sup.2 are respectively a C.sub.1-C.sub.4 alkyl; R.sup.3 and R.sup.3′ are respectively a C.sub.1-C.sub.20 alkyl, alkenyl, or arylalkyl; R.sup.4 and R.sup.4′ are respectively a C.sub.6-C.sub.20 aryl or alkylaryl; n is an integer of 1 to 6; and A is silicon (Si) in Chemical Formula 1.

3. The method of preparing a polypropylene according to claim 1, wherein the alkylaluminoxane cocatalyst is one or more selected from the group consisting of methylaluminoxane, ethylaluminoxane, propylaluminoxane, and butylaluminoxane.

4. The method of preparing a polypropylene according to claim 1, wherein the boron-based cocatalyst is one or more selected from the group consisting of dimethylanilinium tetrakis(pentafluorophenyl)borate, trityl tetrakis(pentafluorophenyl)borate, and methylanilinium tetrakis(pentafluorodiphenyl)borate.

5. The method of preparing a polypropylene according to claim 1, wherein the carrier is one or more selected from the group consisting of silica, silica-alumina and silica-magnesia.

6. The method of preparing a polypropylene according to claim 1, wherein the polymerization of propylene is carried out at the temperature of 25 to 500° C. and the pressure of 1 to 100 kgf/cm.sup.2 for 1 to 24 hrs.

7. The method of preparing a polypropylene according to claim 1, wherein the polymerization is carried out in the presence of hydrogen gas (H.sub.2) of 30 to 2,000 ppm, based on the weight of propylene.

Description

DETAILED DESCRIPTION OF THE EMBODIMENTS

(1) Hereinafter, the preparation method of a polypropylene and the polypropylene obtained by the preparation method according to concrete embodiments of the present invention are explained in more detail. However, the followings are only for the understanding of the present invention and the scope of the present invention is not limited to or by them, and it is obvious to a person skilled in the related art that the embodiments can be variously modified in the scope of the present invention.

(2) In addition, “include” or “comprise” means to include any components (or ingredients) without particular limitation unless there is no particular mention about them in this description, and it cannot be interpreted as a meaning of excluding an addition of other components (or ingredients).

(3) According to one aspect of the present invention, the present invention provides a method of preparing polypropylene including the step of polymerizing propylene in the presence of a catalyst including a metallocene compound represented by the following Chemical Formula 1.

(4) ##STR00002##

(5) In Chemical Formula 1,

(6) M.sup.1 is a group 3 transition metal, a group 4 transition metal, a group 5 transition metal, a lanthanide transition metal, or an actinide transition metal;

(7) X is, same to or different from each other, a halogen;

(8) A is a group 14 element which is a bridge group connecting indenyl groups;

(9) R.sup.1 is a C.sub.1-C.sub.20 alkyl, alkenyl, alkylaryl, arylalkyl, or aryl;

(10) R.sup.2 is hydrogen, or a C.sub.1-C.sub.20 alkyl, alkenyl, alkylaryl, arylalkyl, or aryl;

(11) R.sup.3, R.sup.3′, R.sup.4, and R.sup.4′ are, same to or different from each other, respectively a C.sub.1-C.sub.20 alkyl, alkenyl, alkylaryl, arylalkyl, or aryl; and

(12) n is an integer of 1 to 20.

(13) Preferably, R.sup.1 and R.sup.2 may be respectively a C.sub.1-C.sub.4 alkyl; R.sup.3 and R.sup.3′ may be respectively a C.sub.1-C.sub.20 alkyl, alkenyl, or arylalkyl; R.sup.4 and R.sup.4′ may be respectively a C.sub.1-C.sub.20 aryl or alkylaryl; n may be an integer of 1 to 6; and A may be silicon (Si), in Chemical Formula 1.

(14) The metallocene compound of Chemical Formula 1 includes two indenyl groups in which non-hydrogen substituents are introduced to both of 2-position and 4-position as ligands. Specifically, it has an advantage in that the activity of the catalyst can be maximized because the bridge group connecting the ligands is substituted with the functional group which can take a role of Lewis base as an oxygen-donor. Furthermore, it can show high polymerization activity even when it is supported on a carrier. Accordingly, the compound represented by Chemical Formula 1 can prepare a polyolefin having desired properties more easily when it is used as a catalyst for preparing polyolefin by itself or in a supported form.

(15) According to one embodiment of the present invention, the metallocene compound of Chemical Formula 1 may be used in the preparation method of a polypropylene in the form of a supported catalyst including the metallocene compound solely or in combination with a cocatalyst on a carrier. The cocatalyst may include an alkylaluminoxane cocatalyst and a boron-based cocatalyst.

(16) The carrier is not limited particularly in the present invention if it is common in the related art but one or more carriers selected from the group consisting of silica, silica-alumina and silica-magnesia may be used preferably. Meanwhile, when the catalyst is supported on a carrier like silica, the silica carrier and the functional group of the metallocene compound are chemically bonded. Therefore, it has an advantage in that the catalyst is hardly released from the surface of the carrier during the olefin polymerization process, and there is no fouling that is the adhesion of polymer onto a reactor wall or between polymer particles when the polypropylene is prepared by a slurry or vapor phase polymerization.

(17) And, the polypropylene prepared in the presence of the supported catalyst including such carrier is superior in the particle shape of polymer and the apparent density, and can be properly used to a traditional slurry polymerization, bulk polymerization, and vapor phase polymerization.

(18) Therefore, a carrier dried at high temperature and having siloxane groups of high reactivity may be used. Specifically, silica, silica-alumina, and the like dried at high temperature may be used, and they may include an oxide, a carbonate, a sulfate or a nitrate component, such as Na.sub.2O, K.sub.2CO.sub.3, BaSO.sub.4, Mg(NO.sub.3).sub.2, and so on.

(19) According to one embodiment of the present invention, the metallocene compound of Chemical Formula 1 may be used as a catalyst for the polymerization of propylene, in company with an alkylaluminoxane cocatalyst, a boron-based cocatalyst, and so on.

(20) The alkylaluminoxane cocatalyst may be represented by Chemical Formula 2.

(21) ##STR00003##

(22) In Chemical Formula 2,

(23) M.sup.2 is a group 13 metal element;

(24) R.sup.5 is, same to or different from each other, respectively a C.sub.1-C.sub.20 alkyl, alkenyl, alkylaryl, arylalkyl, or aryl; and

(25) m may be an integer of 2 or more.

(26) Preferably, in the alkylaluminoxane cocatalyst of Chemical Formula 2, R.sup.5 may be respectively methyl, ethyl, propyl, isopropyl, isopropenyl, n-butyl, sec-butyl, tert-butyl, pentyl, hexyl, octyl, decyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, octadecyl, eikosyl, dokosyl, tetrakosyl, cyclohexyl, cyclooctyl, phenyl, tolyl, or ethylphenyl; and M.sup.2 may be aluminum.

(27) And, in Chemical Formula 2, m may be an integer of 2 or more, or 2 to 500, preferably an integer of 6 or more, or 6 to 300, and more preferably an integer of 10 or more, or 10 to 100.

(28) The alkylaluminoxane cocatalyst is characterized in that it includes metal elements which can act as a Lewis acid and can form a bond through Lewis acid-base interaction with the functional group introduced to the bridge group of the metallocene compound of Chemical Formula 1. The cocatalyst compound of Chemical Formula 2 may exist in a linear form, a circular form, or a network form. For example, the cocatalyst may be one or more of methylaluminoxane, ethylaluminoxane, propylaluminoxane, butylaluminoxane, and so on.

(29) Furthermore, the catalyst for the polymerization of a polypropylene of the present invention may include a non-alkylaluminoxane cocatalyst including a non-coordinative anion in company with the alkylaluminoxane cocatalyst. Specifically, according to one embodiment of the present invention, a boron-based cocatalyst may be used as the non-alkylaluminoxane cocatalyst.

(30) The boron-based cocatalyst may be one or more selected from the group consisting of dimethylanilinium tetrakis(pentafluorophenyl)borate ([HN(CH.sub.3).sub.2C.sub.6H.sub.5][B(C.sub.6F.sub.5).sub.4]), trityl tetrakis(pentafluorophenyl)borate ([(C.sub.6H.sub.5).sub.3C][B(C.sub.6F.sub.5).sub.4]), and methylanilinium tetrakis(pentafluorodiphenyl)borate ([HN(CH.sub.3)(C.sub.6H.sub.5).sub.2][B(C.sub.6F.sub.5).sub.4]).

(31) The boron-based cocatalyst stabilizes the metallocene compound and makes it maintain its activity in the polymerization. Specifically, the metallocene compound of the present invention has a tether, and it can show excellent activity without generating fouling because there is no leaching phenomenon in the polymerization because of the functional group. However, if there is no tether in the structure as prior known metallocene compounds, there is a problem of that the leached catalyst precursor and the boron-based cocatalyst react and cause fouling in the main.

(32) The preparation method of the present invention can prepare a supported catalyst having more improved activity by loading both of the alkylaluminoxane cocatalyst and the boron-based cocatalyst, the non-alkylaluminoxane cocatalyst, together onto the carrier. Furthermore, the present inventors selected 2 kinds of cocatalysts that do not cause an opposite effect with each other, and found an optimal loading ratio thereof through experiments.

(33) In the preparation method of a polypropylene according to one embodiment of the present invention, the amount of the metallocene compound supported on the carrier may be about 40 to about 240 μmol, preferably about 80 to about 160 μmol, per the weight of the carrier, for example, based on 1 g of silica.

(34) Furthermore, the amount of the alkylaluminoxane cocatalyst supported on the carrier may be about 8 to about 25 mmol, preferably about 10 to about 20 mmol, per the weight of the carrier, for example, based on 1 g of silica.

(35) The amount of the boron-based cocatalyst supported on the carrier may be about 50 to about 300 μmol, preferably about 64 to about 240 μmol, per the weight of the carrier, for example, based on 1 g of silica.

(36) In the preparation method of a polypropylene according to one embodiment of the present invention, the catalyst has more improved catalytic activity than a supported catalyst including only one kind of cocatalyst and can prepare a polypropylene with improved activity even if the loading conditions of the metallocene compound are changed, namely, reaction temperature, reaction time, kind of silica, loading amount of the metallocene compound, and so on are changed.

(37) Here, the polymerization of propylene may be carried out at the temperature of about 25 to about 500° C. and the pressure of about 1 to about 100 kgf/cm.sup.2 for about 1 to about 24 hrs. At this time, the polymerization reaction temperature is preferably about 25 to about 200° C. and more preferably about 50 to about 100° C. And, the polymerization reaction pressure is preferably about 1 to about 70 kgf/cm.sup.2 and more preferably about 5 to about 50 kgf/cm.sup.2. The polymerization reaction time is preferably about 1 to about 5 hrs.

(38) The preparation method of a polypropylene of the present invention may be carried out by contacting propylene with the catalyst including the metallocene compound represented by Chemical Formula 1.

(39) Furthermore, according to one embodiment of the present invention, the polymerization of propylene may be carried out in the presence of hydrogen gas.

(40) At this time, the hydrogen gas activates inactive sites of the metallocene catalyst and controls the molecular weight of the polymer by causing a chain transfer reaction. The metallocene compound of the present invention is superior in hydrogen reactivity, and thus the polypropylene having the required level of molecular weight distribution can be effectively obtained by controlling the amount of the hydrogen gas used in the polymerization process.

(41) Here, the amount of the hydrogen gas used may be about 10 to about 2,000 ppm, preferably about 50 to about 1,500 ppm, based on the total weight of propylene. The molecular weight distribution and the melt index (MI) of the prepared polypropylene can be controlled in the required range with showing sufficient catalytic activity by controlling the amount of the hydrogen gas used, and thus it is possible to prepare the polypropylene having a proper property according to the use. More specifically, since the metallocene catalyst of the present invention has very excellent hydrogen reactivity, the chain transfer reaction is activated by increasing the amount of hydrogen gas used and the polypropylene having decreased molecular weight and high melt index can be obtained.

(42) The preparation method of a polypropylene may be carried out according to a solution polymerization process, a slurry process, or a gas phase process by using a continuous slurry polymerization reactor, a loop slurry reactor, a gas phase reactor, or a solution reactor.

(43) In the preparation method of a polypropylene according to the present invention, the catalyst may be introduced into a reactor after dissolving or diluting the same in a C.sub.5-C.sub.12 aliphatic hydrocarbon solvent, for example, pentane, hexane, heptane, nonane, decane, and an isomer thereof; an aromatic hydrocarbon solvent such as toluene and benzene; and a chlorinated hydrocarbon solvent such as dichloromethane and chlorobenzene. Here, it is preferable to use the solvent after eliminating a little water or air that acts as a catalytic poison therefrom by treating the same with a small quantity of alkylaluminum.

(44) According to another embodiment of the present invention, a polypropylene obtained by the preparation method is provided.

(45) As disclosed above, according to the present invention, the polypropylene having excellent hydrogen reactivity and high polymerization activity can be obtained by using the catalyst including said novel metallocene compound, compared with the polymer prepared by using an existing metallocene compound.

(46) The polypropylene has low processing temperature and is superior in transparency and fluidity, and thus it can be used to packaging containers, films, sheets, injection molded parts, fiber products, and so on that requires such characteristics.

(47) According to one embodiment of the present invention, the prepared polypropylene may have the weight average molecular weight (Mw) of about 30,000 to about 9,000,000 g/mol, or about 80,000 to about 1,000,000 g/mol, or about 10,000 to about 1,000,000 g/mol according to the amount of hydrogen gas introduced during the polymerization process, when the polymerization process of propylene is carried out by using the catalyst including the metallocene compound.

(48) Furthermore, the polypropylene prepared by the method may show the molecular weight distribution (Mw/Mn) of about 5 or less, for example, about 1 to about 5, preferably about 2 to about 3. Since the polymer has such narrow molecular weight distribution, it is possible to prepare the products having high transparency and less problems of taste or odor unique to polypropylene particularly.

(49) Furthermore, the solubility in xylene (Xs) of the polypropylene may be about 2.0 wt % or less, preferably about 1.5 wt % or less, and more preferably about 1.0 wt % or less, and it represents high tacticity. The solubility in xylene is the content (wt %) of the xylene soluble portion of the polymer dissolved in a cooled xylene prepared by dissolving the polypropylene in xylene and crystallizing the insoluble portion of the polymer therefrom by cooling the solution. The xylene soluble portion includes the polymer chains having low tacticity, and thus the lower solubility in xylene, the higher tacticity.

(50) Furthermore, in the polypropylene prepared according to the present invention, the amount of the fine powder having the diameter of 75 μm or less is about 5.0 wt %, preferably about 3.0 wt % or less, and more preferably about 2.0 wt % or less. Like this, there is less fine powder generation, and thus fouling generation caused by the fine powders and process instability due to this may be prevented and the problem of scattering particles in the product processing may be reduced.

(51) Furthermore, the polypropylene prepared according to the present invention may show high fluidity. For example, the polypropylene prepared according to the present invention shows wide range of melt index (MI) such as about 1 g/10 min or more, preferably about 1 to about 2,500 g/10 min, more preferably about 5 to about 1,500 g/10 min, measured at 230° C. with the load of 2.16 kg. The melt index can be controlled by the amount of hydrogen gas introduced during the polymerization process, and it is possible to prepare the polypropylene having a proper melt index according to the use.

(52) In the present invention, items besides above disclosure can be added or subtracted with necessity and the present invention does not limit them particularly.

(53) Hereinafter, preferable examples are presented for understanding the present invention. However, the following examples are only for illustrating the present invention more easily and the present invention is not limited to or by them.

EXAMPLES

Synthesis Examples

Synthesis of Metallocene Compound

Synthesis Example 1

(54) ##STR00004##

Step 1: Preparation of (6-t-butoxyhexyl)dichloromethylsilane

(55) After slowly adding 100 mL of t-butoxyhexyl magnesium chloride solution (about 0.14 mol, ether) to 100 mL of trichloromethylsilane solution (about 0.21 mol, hexane) in drops at −100° C. for 3 hrs, the mixture was stirred at room temperature for 3 hrs.

(56) After separating a transparent organic layer from the mixture solution, an excess of trichloromethylsilane was eliminated therefrom by vacuum drying the transparent organic layer. By this, (6-t-butoxyhexyl)dichloromethylsilane (yield 84%) of transparent liquid phase was obtained.

(57) .sup.1H NMR (500 MHz, CDCl.sub.3, 7.24 ppm): 0.76(3H, s), 1.11(2H, t), 1.18(9H, s), 1.32˜1.55(8H, m), 3.33(2H, t)

Step 2: Preparation of (6-t-butoxyhexyl)(methtyl)-bis(2-methyl-4-phenylindenyl)silane

(58) 15.4 mL of n-butyllithium solution (2.5 M, hexane solvent) was slowly added to 77 mL of 2-methyl-4-phenylindene toluene/THF=10/1 solution (34.9 mmol) in drops at 0° C., and the mixture solution was stirred at 80° C. for 1 hr and further stirred at room temperature for a day. After then, 5 g of (6-t-butoxyhexyl)dichloromethylsilane prepared above was slowly added to the mixture solution in drops at −78° C. and the mixture was stirred for 10 mins and further stirred at 80° C. for 1 hr. After separating the organic layer therefrom by adding water thereto, a sticky yellow oil (racemic:meso=1:1) was obtained with the yield of 78% by refining the product with a silica column and vacuum drying the same.

(59) .sup.1H NMR (500 MHz, CDCl.sub.3, 7.24 ppm): 0.10(3H, s), 0.98(2H, t), 1.25(9H, s), 1.36˜1.50(8H, m), 1.62(8H, m), 2.26(6H, s), 3.34(2H, t), 3.81(2H, s), 6.87(2H, s), 7.25(2H, t), 7.35(2H, t), 7.45(4H, d), 7.53(4H, t), 7.61(4H, d)

Step 3: Preparation of [(6-t-butoxyhexylmethylsilane-diyl)-bis(2-methyl-4-phenylindenyl)]zirconium dichloride

(60) 3.0 mL of n-butyllithium solution (2.5 M in hexane) was slowly added to 50 mL of (6-t-butoxyhexyl)(methyl)-bis(2-methyl-4-phenyl)indenylsilane ether/hexane=1/1 solution (3.37 mmol) prepared above in drops at −78° C., and the mixture was stirred at room temperature for about 2 hrs and vacuum dried. After then, the yellow solid was obtained by washing the salt with hexane and filtering and vacuum drying the same. After weighing the synthesized ligand salt and bis(N,N′-diphenyl-1,3-propanediamido)dichlorozirconium bis(tetrahydrofuran) [Zr(C.sub.5H.sub.6NCH.sub.2CH.sub.2CH.sub.2NC.sub.5H.sub.6)Cl.sub.2(C.sub.4H.sub.8O).sub.2] in a glove box, ether was slowly added thereto in drops at −78° C. and the mixture was stirred at room temperature for a day. After then, the red reaction solution was filtered and separated therefrom, and 4 equivalent of HCl ether solution (1 M) was slowly added thereto in drops at −78° C. and the mixture was stirred for 3 hrs. And then, the metallocene compound of orange solid form (racemic:meso=10:1) was obtained with the yield of 85% by filtering and vacuum drying the same.

(61) .sup.1H NMR (500 MHz, C.sub.6D.sub.6, 7.24 ppm): 1.19(9H, s), 1.32(3H, s), 1.48˜1.86(10H, m), 2.25(6H, s), 3.37(2H, t), 6.95(2H, s), 7.13(2H, t), 7.36(2H, d), 7.43(6H, t), 7.62(4H, d), 7.67(2H, d)

Comparative Synthesis Example 1

(62) ##STR00005##

Step 1: Preparation of dimethylbis(2-methyl-4-phenylindenyl)silane

(63) 21.8 mL of n-butyllithium solution (2.5 M, hexane solvent) was slowly added to 77 mL of 2-methyl-4-phenylindene toluene/THF=10/1 solution (49.5 mmol) in drops at 0° C., and the mixture solution was stirred at 80° C. for 1 hr and further stirred at room temperature for a day. After then, 2.98 mL of dichloromethylsilane was slowly added thereto in drops at 0° C. or less, and the mixture was stirred for about 10 mins and further stirred at 80° C. for 1 hr. After separating the organic layer therefrom by adding water thereto, a sticky yellow oil (racemic:meso=1:1) was obtained with the yield of 61% by refining the product with a silica column and vacuum drying the same.

(64) .sup.1H NMR (500 MHz, CDCl.sub.3, 7.24 ppm): 0.02(6H, s), 2.37(6H, s), 4.00(2H, s), 6.87(2H, t), 7.38(2H, t), 7.45(2H, t), 7.57(4H, d), 7.65(4H, t), 7.75(4H, d)

Step 2: Preparation of [dimethylsilanediylbis(2-methyl-4-phenylindenyl)]zirconium dichloride

(65) 10.9 mL of n-butyllithium solution (2.5 M in hexane) was slowly added to 240 mL of dimethylbis(2-methyl-4-phenylindenyl)silane ether/hexane=1/1 solution (12.4 mmol) in drops at −78° C. The mixture was stirred at room temperature for a day, and a light yellow solid was obtained by filtering and vacuum drying the same. After weighing the synthesized ligand salt and bis(N,N′-diphenyl-1,3-propanediamido)dichlorozirconiumbis(tetrahydrofuran) in a glove box, ether was slowly added thereto in drops at −78° C. and the mixture was stirred at room temperature for a day. After filtering the mixture and separating the red solution therefrom, the clean red solution was obtained by vacuum drying the same and adding toluene/ether=1/2 solution thereto. 1.5 to 2 equivalent of HCl ether solution (1 M) was slowly added thereto in drops at −78° C. and the mixture was stirred at room temperature for 3 hrs. And then, the catalyst of orange solid component (racemic only) was obtained with the yield of 70% by filtering and vacuum drying the same.

(66) .sup.1H NMR (500 MHz, C.sub.6D.sub.6, 7.24 ppm): 1.32(6H, s), 2.24(6H, s), 6.93(2H, s), 7.10(2H, t), 7.32(2H, t), 7.36(2H, d), 7.43(4H, t), 7.60(4H, d), 7.64(2H, d)

Preparation Examples

Preparation of a Supported Catalyst

Preparation Example 1

(67) The supported catalyst was prepared by loading methylaluminoxane, the metallocene compound obtained in Synthesis Example 1, and a boron-based cocatalyst onto a silica in order.

(68) More specifically, after weighing 3 g of silica L203F in a schlenk flask, 40 mmol of methylaluminoxane (MAO) was added thereto and the mixture was reacted at 95° C. for 24 hrs. After precipitation, the upper part was eliminated and the rest was washed twice with toluene. Subsequently, after dissolving 360 μmol of the metallocene compound obtained in Synthesis Example 1 in toluene, the solution was reacted at 75° C. for 5 hrs. When the precipitation was finished after the reaction, the solution of upper part was eliminated and the left reaction product was washed with toluene. 252 μmol of dimethyl anilinium tetrakis(pentafluorophenyl) borate was reacted at 75° C. for 5 hrs. The reaction product was washed with toluene and further washed with hexane after the reaction, and 5 g of solid type metallocene catalyst supported on silica was obtained by vacuum drying the same.

Comparative Preparation Example 1

(69) A supported catalyst was prepared according to the same method as in Preparation Example 1, except that the metallocene compound obtained in Comparative Synthesis Example 1 was used instead of the metallocene compound obtained in Synthesis Example 1.

Examples of Propylene Polymerization

Example 1

(70) After vacuum drying a 2 L stainless reactor at 65° C. and cooling the same, 1.5 mmol of triethylaluminum (TEAL) was added thereto and 0.37 L of hydrogen and 1.5 L of propylene were introduced thereto in order at room temperature. Subsequently, the mixture was stirred for 10 mins and the metallocene supported catalyst prepared in Example 1 was introduced to the reactor by nitrogen pressure. After then, the temperature of the reactor was elevated to 70° C. within 5 mins and the polymerization was carried out for 1 hr. After the reaction was terminated, unreacted propylene was vented out.

Examples 2 to 4

(71) The propylene polymerization was carried out according to the same method as in Example 1, except that the details of the operating conditions were changed.

Comparative Example 1

(72) The propylene polymerization was carried out according to the same method as in Example 1, except that the supported catalyst obtained in Comparative Preparation Example 1 was used.

Comparative Example 2

(73) The propylene polymerization was carried out according to the same method as in Comparative Example 1, except that the details of the operating conditions were changed.

(74) The details of operating conditions of Examples 1 to 4 and Comparative Examples 1 to 2 are listed in the following Table 1.

(75) TABLE-US-00001 TABLE 1 Propyl- Hydro- Temper- Catalyst ene TEAL gen ature Pressure Input Input Input Input (° C.) (kg/cm.sup.2) (g/hr) (kg/hr) (ppm) (ppm) Exam- 70 35 0.9 80 50 50 ple 1 Exam- 70 35 0.9 80 50 100 ple 2 Exam- 70 35 0.8 80 50 500 ple 3 Exam- 70 35 0.8 80 50 1500 ple 4 Compar- 70 35 1.1 80 50 100 ative Ex- ample1 Compar- 70 35 1.1 80 50 1500 ative Ex- ample2

(76) <Measurements on the Properties of the Polymer>

(77) The properties of the polymers obtained in Examples 1 to 4 and Comparative Examples 1 to 2 were measured by the following methods and the results are listed in Tables 2 and 3.

(78) (1) Catalytic Activity

(79) The ratio of the weight (kg PP) of the produced polymer per the amount (g) of the supported catalyst used and the ratio of the weight (kg PP) of the produced polymer per the content (μmol) of the metallocene compound included in the supported catalyst were calculated, based on unit time (h).

(80) (2) Melt Index (MI)

(81) It was measured at 230° C. with the load of 2.16 kg according to ASTM D1238 and represented by the weight (g) of the polymer that was melted and discharged for 10 mins.

(82) (3) Weight Average Molecular Weight

(83) After heating the sample dissolved in TCB to 220° C., the relative molecular weight compared with the reference was measured by passing each sample through a column tube with about 1.0 cc/min.

(84) (4) Melting Point (Tm)

(85) DSC (Differential Scanning calorimeter, manufactured by TA Co.) curve was obtained with elevating the temperature to 200° C., maintaining the temperature for 5 mins, lowering the temperature to 30° C., and elevating the temperature again. At this time, the scanning speed of heating and cooling processes was 10° C./min and the temperature of the highest peak of the curve obtained during the second heating process was determined as the melting point.

(86) (5) Density

(87) After making the polymer into a sheet of 3 mm thickness and 2 cm diameter by using a press mold of 210° C., the weight was measured with 10° C./min by a mettler scale.

(88) (6) Solubility in xylene (Xs)

(89) After putting the sample in xylene, it was heated at 135° C. for 1 hr and cooled for 30 mins for a pretreatment. After stabilizing the base line of RI, DP, IP by making xylene flow into OminiSec (Viscotek Co. FIPA) device for 4 hrs with the flow rate of 1 ml/min, the concentration of the pretreated sample and the amount thereof injected were filled therein, and the device was operated and the area of the peak was calculated.

(90) (7) Particle Size

(91) After putting the sample in the hopper of the laser diffraction particle size analyzer (Symatec Co., HELOS), APS (Average Particle Size), the span value and the content of the particles of 200 μm or less (fine particles) were checked by setting up the method of 50 to 3500 μm range.

(92) TABLE-US-00002 TABLE 2 Weight Average Molecular Melting Activity Melt Index Weight Point Density (kg/g cat) (g/10 min) (g/mol) (° C.) (g/cm.sup.3) Example 1 32.8 3 800,000 149.9 1.2 Example 2 33.2 125 375,000 150.0 1.2 Example 3 33.7 365 55,000 150.1 1.2 Example 4 34.5 1520 15,000 150.0 1.2 Comparative 28.2 205 280,000 150.2 0.9 Example 1 Comparative 28.5 805 27,000 150.1 0.9 Example 2

(93) TABLE-US-00003 TABLE 3 Solubility in Particle Size xylene APS Distribution (wt %) (wt %) (μm) 500 μm or less 75 μm or less Example 1 0.8 725 72.4 1.5 Example 2 0.9 803 69.2 1.4 Example 3 1.0 817 68.8 1.4 Example 4 0.9 843 67.1 1.5 Comparative 1.2 520 97.5 10.2 Example 1 Comparative 1.1 535 96.4 9.5 Example 2

(94) Referring to Tables 2 and 3, Examples of the present invention can prepare the propylene polymer with a high activity, have the characteristic of high tacticity because they show lower solubility in xylene than Comparative Examples, and thus show an advantage of less content of the fine powder of which the diameter is 75 μm or less.

(95) Furthermore, comparing Examples 2 and 4 with Comparative Examples 1 and 2, it is recognizable that the catalyst used in Examples shows more excellent hydrogen reactivity. Namely, when the hydrogen input thereof was equally changed from 100 ppm to 1500 ppm, the melt index of Example increased about 12 times, from 125 g/10 min (Example 2) to 1520 g/10 min (Example 4), but the melt index of Comparative Example increased just about 4 times, from 205 g/10 min (Comparative Example 1) to 805 g/10 min (Comparative Example 2). Therefore, according to the preparation method of the present invention, the weight average molecular weight and the melt index of the polymer can be easily controlled according to the hydrogen input because of high hydrogen reactivity of the catalyst, and it is expected that the propylene polymer having desired properties can be prepared by controlling the hydrogen input in the polymerization process.