OLEFIN-BASED POLYMER AND METHOD FOR PREPARING SAME

Abstract

The present invention relates to an olefin-based polymer and a method for preparing same. Specifically, the present invention relates to an olefin-based polymer for which processability can be controlled according to a change in density, and a method for preparing same. Processability of the olefin-based polymer according to an embodiment of the present invention can be controlled according to a change in density.

Claims

1. An olefin-based polymer which has (1) a density of 0.915 to 0.945 g/cm.sup.3; (2) a melt index (I.sub.2.16) of 0.5 to 1.5 g/10 min as measured with a load of 2.16 kg at 190 C.; and (3) a ratio between a melt index (I.sub.21.6) measured with a load of 21.6 kg and a melt index (I.sub.2.16) measured with a load of 2.16 kg at 190 C. (melt flow ratio; MFR) satisfying the following Equation 1:
4625d.sup.2+8449d3840<MFR<4625d.sup.2+8449d3834[Equation 1] wherein MFR is a melt flow ratio, and d is density (g/cm.sup.3).

2. The olefin-based polymer of claim 1, wherein the olefin-based polymer has (1) the density of 0.917 to 0.943 g/cm.sup.3; and (2) the melt index of 0.6 to 1.0 g/10 min as measured with a load of 2.16 kg at 190 C.

3. The olefin-based polymer of claim 1, wherein the olefin-based polymer is prepared by polymerizing an olefin-based monomer in the presence of a hybrid catalyst, said hybrid catalyst including: one or more first transition compound represented by the following Chemical Formula 1; and one or more second transition metal compound selected from a compound represented by the following Chemical Formula 2 or the following Chemical Formula 3: ##STR00009## wherein M.sub.1 and M.sub.2 are different from each other and independently of each other titanium (Ti), zirconium (Zr), or hafnium (Hf), X is independently of each other halogen, C.sub.1-20 alkyl, C.sub.2-20 alkenyl, C.sub.2-20 alkynyl, C.sub.6-20 aryl, C.sub.1-20 alkyl C.sub.6-20 aryl, C.sub.6-20 aryl C.sub.1-20 alkyl, C.sub.1-20 alkylamido, or C.sub.6-20 arylamido, and R.sub.1 to R.sub.10 are independently of one another hydrogen, substituted or unsubstituted C.sub.1-20 alkyl, substituted or unsubstituted C.sub.2-20 alkenyl, substituted or unsubstituted C.sub.6-20 aryl, substituted or unsubstituted C.sub.1-20 alkyl C.sub.6-20 aryl, substituted or unsubstituted C.sub.6-20 aryl C.sub.1-20 alkyl, substituted or unsubstituted C.sub.1-20 heteroalkyl, substituted or unsubstituted C.sub.3-20 heteroaryl, substituted or unsubstituted C.sub.1-20 alkylamido, substituted or unsubstituted C.sub.6-20 arylamido, substituted or unsubstituted C.sub.1-20 alkylidene, or substituted or unsubstituted C.sub.1-20 silyl, but R.sub.1 to R.sub.10 may be independently of one another connected to an adjacent group to form a substituted or unsubstituted saturated or unsaturated C.sub.4-20 ring.

4. The olefin-based polymer of claim 3, wherein M.sub.1 and M.sub.2 are different from each other and are zirconium or hafnium, respectively, X is halogen or C.sub.1-20 alkyl, respectively, and R.sub.1 to R.sub.10 are hydrogen, substituted or unsubstituted C.sub.1-20 alkyl, substituted or unsubstituted C.sub.1-20 alkenyl, or substituted or unsubstituted C.sub.6-20 aryl, respectively.

5. The olefin-based polymer of claim 4, wherein M.sub.1 is hafnium, M.sub.2 is zirconium, and X is chlorine or methyl.

6. The olefin-based polymer of claim 3, wherein the first transition metal compound is one or more of transition metal compounds represented by the following Chemical Formulae 1-1 or 1-2, and the second transition metal compound is one or more of transition metal compounds represented by the following Chemical Formulae 2-1, 2-2, or 3-1: ##STR00010## wherein Me is a methyl group.

7. The olefin-based polymer of claim 3, wherein a mole ratio of the first transition metal compound to the second transition metal compound is in a range of 100:1 to 1:100.

8. The olefin-based polymer of claim 3, wherein the catalyst includes one or more cocatalyst compound selected from the group consisting of a compound represented by the following Chemical Formula 4, a compound represented by the following Chemical Formula 5, and a compound represented by the following Chemical Formula 6: ##STR00011## wherein n is an integer of 2 or more, R.sub.a is a halogen atom, a C.sub.1-20 hydrocarbon group, or a C.sub.1-20 hydrocarbon group substituted with halogen, D is aluminum (Al) or boron (B), R.sub.b, R.sub.c, and R.sub.d are independently of one another a halogen atom, a C.sub.1-20 hydrocarbon group, a C.sub.1-20 hydrocarbon group substituted with halogen, or a C.sub.1-20 alkoxy group, and L is a neutral or cationic Lewis base, [L-H].sup.+ and [L].sup.+ are a Bronsted acid, Z is a group 13 element, and A is independently of each other a substituted or unsubstituted C.sub.6-20 aryl group or a substituted or unsubstituted C.sub.1-20 alkyl group.

9. The olefin-based polymer of claim 8, wherein the catalyst further includes a carrier which supports the transition metal compound, the cocatalyst compound, or both of them.

10. The olefin-based polymer of claim 9, wherein the carrier includes one or more selected from the group consisting of silica, alumina, and magnesia.

11. The olefin-based polymer of claim 9, wherein a total amount of the hybrid transition metal compound supported on the carrier is 0.001 to 1 mmol based on 1 g of the carrier, and a total amount of the cocatalyst compound supported on the carrier is 2 to 15 mmol based on 1 g of the carrier.

12. The olefin-based polymer of claim 3, wherein the olefin-based polymer is a copolymer of the olefin-based monomer and an olefin-based comonomer.

13. The olefin-based polymer of claim 12, wherein the olefin-based monomer is ethylene, and the olefin-based comonomer is one or more selected from the group consisting of propylene, 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-heptene, 1-octene, 1-decene, 1-undecene, 1-dodecene, 1-tetradecene, and 1-hexadecene.

14. The olefin-based polymer of claim 13, wherein the olefin-based polymer is a linear low-density polyethylene in which the olefin-based monomer is ethylene and the olefin-based comonomer is 1-hexene.

15. A method for preparing an olefin-based polymer, the method comprising: polymerizing an olefin-based monomer in the presence of a hybrid catalyst including: one or more first transition metal compound represented by the following Chemical Formula 1; and one or more second transition metal compound selected from a compound represented by the following Chemical Formula 2 or a compound represented by the following Chemical Formula 3, thereby obtaining an olefin-based polymer, wherein the olefin-based polymer has (1) a density of 0.915 to 0.945 g/cm.sup.3; (2) a melt index (I.sub.2.16) of 0.5 to 1.5 g/10 min as measured with a load of 2.16 kg at 190 C.; and (3) a ratio between a melt index (I.sub.21.6) measured with a load of 21.6 kg and a melt index (I.sub.2.16) measured with a load of 2.16 kg at 190 C. (melt flow ratio; MFR) satisfying the following Equation 1: ##STR00012## wherein MFR is a melt flow ratio, d is density (g/cm.sup.3), M.sub.1 and M.sub.2 are different from each other and independently of each other titanium (Ti), zirconium (Zr), or hafnium (Hf), X is independently of each other halogen, C.sub.1-20 alkyl, C.sub.2-20 alkenyl, C.sub.2-20 alkynyl, C.sub.6-20 aryl, C.sub.1-20 alkyl C.sub.6-20 aryl, C.sub.6-20 aryl C.sub.1-20 alkyl, C.sub.1-20 alkylamido, or C.sub.6-20 arylamido, and R.sub.1 to R.sub.10 are independently of one another hydrogen, substituted or unsubstituted C.sub.1-20 alkyl, substituted or unsubstituted C.sub.2-20 alkenyl, substituted or unsubstituted C.sub.6-20 aryl, substituted or unsubstituted C.sub.1-20 alkyl C.sub.6-20 aryl, substituted or unsubstituted C.sub.6-20 aryl C.sub.1-20 alkyl, substituted or unsubstituted C.sub.1-20 heteroalkyl, substituted or unsubstituted C.sub.3-20 heteroaryl, substituted or unsubstituted C.sub.1-20 alkylamido, substituted or unsubstituted C.sub.6-20 arylamido, substituted or unsubstituted C.sub.1-20 alkylidene, or substituted or unsubstituted C.sub.1-20 silyl, but R.sub.1 to R.sub.10 may be independently of one another connected to an adjacent group to form a substituted or unsubstituted saturated or unsaturated C.sub.4-20 ring.

16. The method for preparing an olefin-based monomer of claim 15, wherein the polymerization of the olefin-based monomer is gas phase polymerization.

Description

DESCRIPTION OF DRAWINGS

[0031] FIG. 1 is a graph showing change in MFR depending on change in density of an olefin-based polymer according to an embodiment of the present invention.

BEST MODE

[0032] Hereinafter, the present invention will be described in more detail.

[0033] Olefin-Based Polymer

[0034] According to an embodiment of the present invention, an olefin-based polymer which has (1) a density of 0.915 to 0.945 g/cm.sup.3; (2) a melt index (I.sub.2.16) of 0.5 to 1.5 g/10 min as measured with a load of 2.16 kg at 190 C.; and (3) a ratio between a melt index (I.sub.21.6) measured with a load of 21.6 kg and a melt index (I.sub.2.16) measured with a load of 2.16 kg at 190 C. (melt flow ratio; MFR) satisfying the following Equation 1 is provided:

4625d.sup.2+8449d3840<MFR<4625d.sup.2+8449d3834[Mathematical Formula 1]

[0035] wherein MFR is a melt flow ratio, and d is density (g/cm.sup.3).

[0036] In a specific example of the present invention, the olefin-based polymer has a density of 0.915 to 0.945 g/cm.sup.3. Preferably, the olefin-based polymer may have a density of 0.917 to 0.943 g/cm.sup.3.

[0037] In a specific example of the present invention, the olefin-based polymer may have a melt index (I.sub.2.16) of 0.5 to 1.5 g/10 min as measured with a load of 2.16 kg at 190 C. Preferably, the olefin-based polymer may have a melt index of 0.6 to 1.0 g/10 min as measured with a load of 2.16 kg at 190 C.

[0038] In a specific example of the present invention, the olefin-based polymer may have a ratio between a melt index (I.sub.21.6) measured with a load of 21.6 kg and a melt index (I.sub.2.16) measured with a load of 2.16 kg at 190 C. (melt flow ratio; MFR) of 15 to 50. Preferably, the olefin-based polymer may have the MFR of 15 to 35.

[0039] The olefin-based polymer according to an embodiment of the present invention may be prepared by polymerizing an olefin-based monomer in the presence of a hybrid catalyst including: at least one first transition compound represented by the following Chemical Formula 1; and at least one second transition metal compound selected from a compound represented by the following Chemical Formula 2 and a compound represented by the following Chemical Formula 3:

##STR00004##

[0040] wherein M.sub.1 and M.sub.2 are different from each other and independently of each other titanium (Ti), zirconium (Zr), or hafnium (Hf). Specifically, M.sub.1 and M.sub.2 may be different from each other and be zirconium or hafnium, respectively. Preferably, M.sub.1 may be hafnium and M.sub.2 may be zirconium.

[0041] X is independently of each other halogen, C.sub.1-20 alkyl, C.sub.2-20 alkenyl, C.sub.2-20 alkynyl, C.sub.6-20 aryl, C.sub.1-20 alkyl C.sub.6-20 aryl, C.sub.6-20 aryl C.sub.1-20 alkyl, C.sub.1-20 alkylamido, or C.sub.6-20 arylamido. Specifically, X may be halogen or C.sub.1-20 alkyl, respectively. Preferably, X may be chlorine or methyl.

[0042] R.sup.1 to R.sup.10 are independently of one another hydrogen, substituted or unsubstituted C.sub.1-20 alkyl, substituted or unsubstituted C.sub.2-20 alkenyl, substituted or unsubstituted C.sub.6-20 aryl, substituted or unsubstituted C.sub.1-20 alkyl C.sub.6-20 aryl, substituted or unsubstituted C.sub.6-20 aryl C.sub.1-20 alkyl, substituted or unsubstituted C.sub.1-20 heteroalkyl, substituted or unsubstituted C.sub.3-20 heteroaryl, substituted or unsubstituted C.sub.1-20 alkylamido, substituted or unsubstituted C.sub.6-20 arylamido, substituted or unsubstituted C.sub.1-20 alkylidene, or substituted or unsubstituted C.sub.1-20 silyl, in which R.sup.1 to R.sup.10 may be independently of one another connected to an adjacent group to form a substituted or unsubstituted saturated or unsaturated C.sub.4-20 ring. Specifically, R.sub.1 to R.sub.10 may be hydrogen, substituted or unsubstituted C.sub.1-20 alkyl, substituted or unsubstituted C.sub.1-20 alkenyl, or substituted or unsubstituted C.sub.6-20 aryl, respectively.

[0043] In a specific example of the present invention, M.sub.1 and M.sub.2 may be different from each other and be zirconium or hafnium, respectively, X may be halogen or C.sub.1-20 alkyl, respectively, and R.sup.1 to R.sup.10 may be hydrogen, substituted or unsubstituted C.sub.1-20 alkyl, substituted or unsubstituted C.sub.1-20 alkenyl, or substituted or unsubstituted C.sub.6-20 aryl, respectively.

[0044] In a preferred specific example of the present invention, M.sub.1 may be hafnium, M.sub.2 may be zirconium, and X may be chlorine or methyl.

[0045] In a preferred specific example of the present invention, the first transition metal compound may be at least one of transition metal compounds represented by the following Chemical Formulae 1-1 and 1-2, and the second transition metal compound may be at least one of transition metal compounds represented by the following Chemical Formulae 2-1, 2-2, and 3-1:

##STR00005##

[0046] wherein Me is a methyl group.

[0047] In a specific example of the present invention, a mole ratio of the first transition metal compound to the second transition metal compound is in a range of 100:1 to 1:100. Preferably, a mole ratio of the first transition metal compound to the second transition metal compound is in a range of 50:1 to 1:50. Preferably, a mole ratio of the first transition metal compound to the second transition metal compound is in a range of 10:1 to 1:10.

[0048] In a specific example of the present invention, the catalyst may include at least one cocatalyst compound selected from the group consisting of a compound represented by the following Chemical Formula 4, a compound represented by the following Chemical Formula 5, and a compound represented by the following Chemical Formula 6:

##STR00006##

[0049] wherein n is an integer of 2 or more, R.sub.a is a halogen atom, C1-20 hydrocarbon, or C1-20 hydrocarbon substituted with halogen. Specifically, R.sub.a may be methyl, ethyl, n-butyl, or isobutyl.

##STR00007##

[0050] wherein D is aluminum (Al) or boron (B), and R.sub.b, R.sub.c, and R.sub.d are independently of one another a halogen atom, a C.sub.1-20 hydrocarbon group, a C.sub.1-20 hydrocarbon group substituted with halogen, or a C.sub.1-20 alkoxy group. Specifically, when D is aluminum (Al), R.sub.b, R.sub.c, and R.sub.d may be independently of one another methyl or isobutyl, and when D is boron (B), R.sub.b, R.sub.c, and R.sub.d may be pentafluorophenyl, respectively.

[L-H].sup.+[Z(A).sub.4].sup. or [L]+[Z(A).sub.4].sup.[Chemical Formula 6]

[0051] L is a neutral or cationic Lewis base, [L-H].sup.+ and [L].sup.+ are a Bronsted acid, Z is a group 13 element, and A is independently of each other a substituted or unsubstituted C.sub.6-20 aryl group or a substituted or unsubstituted C.sub.1-20 alkyl group. Specifically, [L-H].sup.+ may be dimethylanilinium cation, [Z (A).sub.4].sup. may be [B(C.sub.6F.sub.5).sub.4].sup., and [L].sup.+ may be [(C.sub.6Hs).sub.3C].sup.+.

[0052] Specifically, an example of the compound represented by Chemical Formula 4 includes methylaluminoxane, ethylaluminoxane, isobutylaluminoxane, butylaluminoxane, and the like, and is preferably methylaluminoxane, but is not limited thereto.

[0053] An example of the compound represented by Chemical Formula 5 includes trimethylaluminum, triethylaluminum, triisobutylaluminum, tripropylaluminum, tributylaluminum, dimethylchloroaluminum, triisopropylaluminum, tri-s-butylaluminum, tricyclopentylaluminum, tripentylaluminum, triisopentylaluminum, trihexylaluminum, trioctylaluminum, ethyldimethylaluminum, methyldiethylaluminum, triphenylaluminum, tri-p-tolylaluminum, dimethylaluminummethoxide, dimethylaluminumethoxide, trimethylboron, triethylboron, triisobutylboron, tripropylboron, tributylboron, and the like, and is preferably trimethylaluminum, triethylaluminum, and triisobutylaluminum, but is not limited thereto.

[0054] An example of the compound represented by Chemical Formula 6 includes triethylammoniumtetraphenylboron, tributylammoniumtetraphenylboron, trimethylammoniumtetraphenylboron, tripropylammoniumtetraphenylboron, trimethylammoniumtetra(p-tolyl)boron, trimethylammoniumtetra(o,p-dimethylphenyl)boron, tributylammoniumtetra(p-trifluoromethylphenyl)boron, trimethylammoniumtetra(p-trifluoromethylphenyl)boron, tributylammoniumtetrapentafluorophenylboron, N,N-diethylaniliniumtetraphenylboron, N,N-diethylaniliniumtetrapentafluorophenylboron, diethylammoniumtetrapentafluorophenylboron, triphenylphosphoniumtetraphenylboron, trimethylphosphoniumtetraphenylboron, triethylammoniumtetraphenylaluminum, tributylammoniumtetraphenylaluminum, trimethylammoniumtetraphenylaluminum, tripropylammoniumtetraphenylaluminum, trimethylammoniumtetra(p-tolyl)aluminum, tripropylammoniumtetra(p-tolyl)aluminum, triethylammoniumtetra(o,p-dimethylphenyl)aluminum, tributylammoniumtetra(p-trifluoromethylphenyl)aluminum, trimethylammoniumtetra(p-trifluoromethylphenyl)aluminum, tributylammoniumtetrapentafluorophenylaluminum, N,N-diethylaniliniumtetraphenylaluminum, N,N-diethylaniliniumtetrapentafluorophenylaluminum, diethylammoniumtetrapentatetraphenylaluminum, triphenylphosphoniumtetraphenylaluminum, trimethylphosphoniumtetraphenylaluminum, tripropylammoniumtetra(p-tolyl)boron, triethylammoniumtetra(o,p-dimethylphenyl)boron, tributylammoniumtetra(p-trifluoromethylphenyl)boron, triphenylcarboniumtetra(p-trifluoromethylphenyl)boron, triphenylcarboniumtetrapentafluorophenylboron, and the like.

[0055] In a specific example of the present invention, the catalyst may further include a carrier which supports a transition metal compound, a cocatalyst compound, or both of them. Specifically, the carrier may support both the transition metal compound and the cocatalyst compound.

[0056] Here, the carrier may include a material containing a hydroxyl group on the surface, and preferably, may use a material having highly reactive hydroxyl group and siloxane group which is dried to remove moisture from the surface. For example, the carrier may include at least one selected from the group consisting of silica, alumina, and magnesia. Specifically, silica, silica-alumina, silica-magnesia, and the like which are dried at a high temperature may be used as the carrier, and these may usually contain oxide, carbonate, sulfate, and nitrate components such as Na.sub.2O, K.sub.2CO.sub.3, BaSO.sub.4, and Mg(NO.sub.3).sub.2. In addition, these may include carbon, zeolite, magnesium chloride, and the like. However, the carrier is not limited thereto, and is not particularly limited as long as it may support a transition metal compound and a cocatalyst compound.

[0057] The carrier may have an average particle size of 10 to 250 m, preferably 10 to 150 m, and more preferably 20 to 100 m.

[0058] The carrier may have a micropore volume of 0.1 to 10 cc/g, preferably 0.5 to 5 cc/g, and more preferably 1.0 to 3.0 cc/g.

[0059] The carrier may have a specific surface area of 1 to 1,000 m.sup.2/g, preferably 100 to 800 m.sup.2/g, and more preferably 200 to 600 m.sup.2/g.

[0060] In a preferred specific example of the present invention, the carrier may be silica. Here, a drying temperature of the silica may be 200 to 900 C. The drying temperature may be 300 to 800 C., and more preferably 400 to 700 C. When the drying temperature is lower than 200 C., silica has too much moisture so that the moisture on the surface reacts with the cocatalyst compound, and when the drying temperature is higher than 900 C., the structure of the carrier may collapse.

[0061] A concentration of a hydroxyl group in dried silica may be 0.1 to 5 mmol/g, preferably 0.7 to 4 mmol/g, and more preferably 1.0 to 2 mmol/g. When the concentration of the hydroxyl group is less than 0.1 mmol/g, the supported amount of a cocatalyst compound is lowered, and when the concentration is more than 5 mmol/g, the catalyst component becomes inactive.

[0062] The total amount of the transition metal compound supported on the carrier may be 0.001 to 1 mmol based on 1 g of the carrier. When a ratio between the transition metal compound and the carrier satisfies the above range, appropriate supported catalyst activity is shown, which is advantageous in terms of the activity maintenance of a catalyst and economic feasibility.

[0063] The total amount of the cocatalyst compound supported on the carrier may be 2 to 15 mmol based on 1 g of the carrier. When the ratio of the cocatalyst compound and the carrier satisfies the above range, it is advantageous in terms of the activity maintenance of a catalyst and economic feasibility.

[0064] The carrier may be one or two or more. For example, both the transition metal compound and the cocatalyst compound may be supported on one carrier, and each of the transition metal compound and the cocatalyst compound may be supported on two or more carriers. In addition, only one of the transition metal compound and the cocatalyst compound may be supported on the carrier.

[0065] As a method for supporting the transition metal compound and/or the cocatalyst compound which may be used in the catalyst for olefin polymerization, a physical adsorption method or a chemical adsorption method may be used.

[0066] For example, the physical adsorption method may be a method of bringing a solution in which a transition metal compound is dissolved into contact with a carrier and then drying, a method of bringing a solution in which a transition metal compound and a cocatalyst compound are dissolved into contact with a carrier and then drying, a method of bringing a solution in which a transition metal compound is dissolved into contact with a carrier and then drying to prepare a carrier on which the transition metal compound is supported, separately bringing a solution in which a cocatalyst compound is dissolved into contact with a carrier and then drying to prepare a carrier on which the cocatalyst compound is supported, and then mixing them, or the like.

[0067] The chemical adsorption method may be a method of first supporting a cocatalyst compound on the surface of a carrier and then supporting a transition metal compound on the cocatalyst compound, a method of binding a functional group (for example, a hydroxyl group (OH) on the surface of silica, in the case of silica) on the surface of a carrier and a catalyst compound covalently.

[0068] In a specific example of the present invention, the olefin-based polymer may be a homopolymer of an olefin-based monomer or a copolymer of olefin-based monomer and comonomer. Preferably, the olefin-based polymer is a copolymer of an olefin-based monomer and an olefin-based comonomer.

[0069] Here, the olefin-based monomer may be at least one selected from the group consisting of C.sub.2-20 -olefin, C.sub.1-20 diolefin, C.sub.3-20 cycloolefin, and C.sub.3-20 cyclodiolefin.

[0070] For example, the olefin-based monomer may be ethylene, propylene, 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-heptene, 1-octene, 1-decene, 1-undecene, 1-dodecene, 1-tetradecene, or 1-hexadecene, and the olefin-based polymer may be a homopolymer including only one or a copolymer including two or more of the olefin-based monomers exemplified above.

[0071] In an exemplary embodiment, the olefin-based polymer may be a copolymer of ethylene and C.sub.3-20 -olefin. Preferably, the olefin-based polymer may be a linear low-density polyethylene in which the olefin-based monomer is ethylene and the olefin-based comonomer is 1-hexene.

[0072] In this case, the content of ethylene is preferably 55 to 99.9 wt %, and more preferably 90 to 99.9 wt %. The content of the -olefin-based comonomer is preferably 0.1 to 45 wt %, and more preferably 0.1 to 10 wt %.

[0073] Method for Preparing Olefin-Based Polymer

[0074] According to an embodiment of the present invention, a method for preparing an olefin-based polymer including: polymerizing an olefin-based monomer in the presence of a hybrid catalyst including: at least one first transition compound represented by the following Chemical Formula 1; and at least one second transition metal compound selected from a compound represented by the following Chemical Formula 2 and a compound represented by the following Chemical Formula 3, thereby obtaining an olefin-based polymer is provided:

##STR00008##

[0075] wherein M.sub.1, M.sub.2, X, and R.sub.1 to R.sub.10 are as defined above in the item of olefin-based polymer.

[0076] As described above, the olefin-based polymer prepared by the preparation method according to an embodiment of the present invention has (1) a density of 0.915 to 0.945 g/cm.sup.3; (2) a melt index (I.sub.2.16) of 0.5 to 1.5 g/10 min as measured with a load of 2.16 kg at 190 C.; and (3) a ratio between a melt index (I.sub.21.6) measured with a load of 21.6 kg and a melt index (I.sub.2.16) measured with a load of 2.16 kg at 190 C. (melt flow ratio; MFR) satisfying the following Equation 1 is provided:

4625d.sup.2+8449d3840<MFR<4625d.sup.2+8449d3834[Mathematical Formula 1]

[0077] wherein MFR and d are as defined above in the item of olefin-based polymer.

[0078] In a specific example of the present invention, the olefin-based polymer may be polymerized by a polymerization reaction such as free radical, cationic, coordination, condensation, and addition polymerization, but is not limited thereto.

[0079] In an exemplary embodiment of the present invention, the olefin-based polymer may be prepared by a gas phase polymerization method, a solution polymerization method, a slurry polymerization method, or the like. Preferably, the polymerization of the olefin-based monomer may be gas phase polymerization, specifically, the polymerization of the olefin-based monomer may be performed in a gas phase fluidized bed reactor.

[0080] When the olefin-based polymer is prepared by a solution polymerization method or a slurry polymerization method, an example of the solvent to be used may include a C.sub.5-12 aliphatic hydrocarbon solvent such as pentane, hexane, heptane, nonane, decane, and isomers thereof; an aromatic hydrocarbon solvent such as toluene and benzene; a hydrocarbon solvent substituted with a chlorine atom such as dichloromethane and chlorobenzene; and a mixture thereof, but is not limited thereto.

BEST MODE FOR CARRYING OUT THE INVENTION

Examples

[0081] Hereinafter, the present invention will be specifically described through the following examples. However, the following examples are only illustrative of the present invention, and do not limit the scope of the present invention.

PREPARATION EXAMPLE

[0082] The transition metal compound of Chemical Formula 1-2 (dimethylbis(n-propylcyclopentadienyl) hafnium dichloride) and the transition metal compound of Chemical Formula 3-1 ((pentamethylcyclopentadienyl) (n-propylcyclopentadienyl) zirconium dichloride) were purchased from MCN, and used without further purification.

Preparation Example 1

[0083] 892 g of a 10% toluene solution of methylaluminoxane was added to 4.07 g of the transition metal compound of Chemical Formula 1-2 and 1.68 g of the transition metal compound of Chemical Formula 3-1, and the solution was stirred at room temperature for 1 hour. The solution after the reaction was added to 200 g of silica (XPO-2402), 1.5 L of toluene was further added, and stirring was performed at 70 C. for 2 hours. The supported catalyst was washed with 500 mL of toluene, and was dried overnight at 60 C. under vacuum to obtain 280 g of a supported catalyst in powder form.

Examples 1-4

[0084] Ethylene/1-hexene copolymers were prepared in the presence of the supported catalysts, which were obtained in Preparation Example 1, respectively, using a gas phase fluidized bed reactor. The ethylene partial pressure of the reactor was maintained at about 15 kg/cm.sup.2, and the polymerization temperature was maintained at about 80 C.

[0085] The polymerization conditions of the examples are shown in the following Table 1.

TABLE-US-00001 TABLE 1 Example 1 Example 2 Example 3 Example 4 Polymerization temperature ( C.) 80.4 80.3 81.6 81.3 Catalyst injection amount (g/h) 1.31 1.8 1.6 2.2 Hydrogen injection amount (g/h) 2.13 1.08 0.97 0.95 1-Hexene injection amount (kg/h) 1.54 0.03 0.03 0.02 Hydrogen/ethylene concentration 0.049 0.026 0.023 0.023 (%) ratio 1-Hexene/ethylene concentration 1.39 0.43 0.33 0.34 (%) ratio Production amount per hour (kg/h) 6.22 7.31 6.13 7.01

Comparative Examples 1 and 2

[0086] For comparison, linear low-density polyethylenes M1810HN (density: 0.9180 g/cm.sup.3, melt index: 1.0 g/10 min; Comparative Example 1) and M3707HN (density: 0.9370 g/cm.sup.3, melt index: 0.70 g/10 min; Comparative Example 2) from Hanwha Solutions were used.

Test Example

[0087] The physical properties of the olefin-based polymer of the above examples were measured by the following methods and criteria. The results are shown in Table 2.

[0088] (1) Density

[0089] Measured according to ASTM D 1505.

[0090] (2) Melt Index and Melt Index Ratio (MFR)

[0091] The melt index was measured with a load of 21.6 kg and a load of 2.16 kg, respectively, at 190 C. in accordance with ASTM D1238, and the ratio (MI21.6/MI2.16) was calculated.

TABLE-US-00002 TABLE 2 Example Example Example Example Comparative Comparative Unit 1 2 3 4 Example 1 Example 2 Density g/cm.sup.3 0.9174 0.9310 0.9371 0.9425 0.9182 0.9371 MI2.16 g/10 min 0.87 0.73 0.75 0.69 0.93 0.71 MI21.6 g/10 min 18.4 14.5 14.0 11.9 15.5 12.1 MFR 21.2 19.8 18.62 17.3 16.7 16.9

INDUSTRIAL APPLICABILITY

[0092] As confirmed from Table 2 and FIG. 1, since the melt index ratio (MI.sub.21.6/MI.sub.2.16) of the olefin-based polymer according to the specific example of the present invention, which is a measure of processability, changes depending on change in density, processability of a resin may be adjusted as required.