JP3452670B2 - Glass fiber reinforced resin composition - Google Patents

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION The present invention relates to interior and exterior parts for automobiles,
The present invention relates to a glass fiber reinforced resin composition having excellent heat resistance, rigidity and impact resistance suitable for use in home electric appliance parts, office equipment parts and the like.

[0002]

2. Description of the Related Art Polypropylene resin compositions have excellent heat resistance, chemical resistance and electrical properties, and further have rigidity, tensile strength, transparency,
Because of its excellent workability, it has been widely used in injection molding, sheet molding, blow molding and other molding methods. However, when the polypropylene resin composition is used as an industrial member such as interior / exterior parts for automobiles, parts for home electric appliances, parts for office equipment, etc., heat resistance, rigidity and impact resistance are still insufficient. Conventionally, metal as these industrial members,
Although glass fiber reinforced nylon and the like are used, there is a problem that the product has a heavy weight because metal has a large specific gravity, and the cost of glass fiber reinforced nylon is high.

As a polypropylene resin composition having excellent mechanical properties such as heat resistance, rigidity and impact resistance, a glass fiber reinforced resin composition containing glass fiber is well known. Such a glass fiber reinforced resin composition is mainly composed of polypropylene, modified polypropylene and glass fibers, and if necessary, a pigment, a heat stabilizer, a light stabilizer,
Additives such as metal deactivators and lubricants have been added. However, the acid graft ratio of these modified polypropylenes is 0.2% or less, and the diameter of the glass fiber is 13μ.
There is a problem that the surface smoothness of the molded product is poor because it is large around m and its surface treatment is insufficient. Furthermore, by increasing the blending amount of glass fiber, heat resistance,
Although mechanical properties such as rigidity and impact resistance can be improved, the surface smoothness of the molded product is deteriorated, and it is disadvantageous in terms of cost and recyclability. For example, the glass fiber in the polypropylene resin composition molded by re-kneading the polypropylene resin composition to which the glass fiber is added is easily broken in the manufacturing process, and sufficient mechanical strength cannot be obtained.

As described above, the polypropylene resin composition having a good balance of heat resistance, rigidity and impact resistance, as well as surface smoothness and recyclability has not yet been obtained. If this problem is solved, it is expected that the range of use of the polypropylene resin material will be expanded, the number of parts that can be covered with one material will be increased, and the cost can be advantageously developed.

Therefore, an object of the present invention is to provide a glass fiber reinforced resin composition having excellent heat resistance, rigidity and impact resistance, which is suitable for use in interior and exterior parts of automobiles, parts for home electric appliances, parts for office equipment and the like. It is to provide things.

[0006]

Means for Solving the Problems As a result of intensive investigations by the present inventors, the above problems were solved by blending a specific compound in a specific range with a highly crystalline polypropylene polymer having specific properties. As a result, they have come to complete the present invention. That is, the glass fiber reinforced resin composition of the present invention has (a) a melt flow rate (MFR) of 0.01 measured according to ASTM D-1238.
20 to 97.4 wt% of a propylene polymer satisfying the relational expression of Meso Mean Chain Length (Nm) and MFR determined by ¹³ C-NMR, Nm ≧ 97 + 29.5 log MFR, (b) 2.5 to 60% by weight of glass fibers having an average fiber diameter of 3 to 11 μm, and (c) 0.1 to 20% by weight of modified polyolefin.

The present invention will be described in detail below. [1] Each Component of Glass Fiber Reinforced Resin Composition (a) Propylene Polymer (1) Physical Properties The propylene polymer used in the present invention is a highly crystalline polypropylene and may be either a homopolymer or a block copolymer. High crystalline polypropylene is ASTM
Melt flow rate (MFR) measured according to D-1238 (230 ° C., load 2.16 kg) is 0.01 to 1.
It is in the range of 50 g / 10 minutes, preferably 1 to 100 g / 10 minutes, and the meso-average chain length (Nm) and MFR determined by ¹³ C-NMR satisfy the relational expression Nm ≧ 97 + 29.5 log MFR. When the MFR is less than 0.01, the moldability is low, and when it exceeds 150, the mechanical strength is lowered. Also,
When Nm <97 + 29.5 log MFR, the heat resistance decreases. Further, it is preferable that the flexural modulus measured according to ASTM D-790 is 20000 kgf / cm ² or more.

Nm is based on James C. Rand
all, “Polymer Sequence Det
termination "p. 37, Academic
It was obtained according to the method described in Press, London, 1977, specifically, meso-mesotriad [mm] and meso-measured by ¹³ C-NMR measurement method.
From the racemic triad [mr] and the following equation:

[Equation 1] Sought according to. Nm is a value of the obtained crystalline polymer as it is, and is not a value of the polymer after extraction, fractionation and the like.

(2) Production Method The propylene polymer is not particularly limited in its production method as long as it satisfies the above physical properties, but it is preferably produced by the following method.

(I) Polymerization catalyst (A) A solid component containing magnesium, titanium, a halogen, and an electron-donating compound as essential components, (B) an organoaluminum compound, and (C) an organosilicon represented by the general formula (IV). Compound and (D) optionally in the presence of an electron-donating compound,
(E) The catalyst component (hereinafter referred to as “preliminary polymerization catalyst component”) is obtained by prepolymerizing the olefin by contacting with the olefin.
) Is prepared, and an organometallic compound and, if necessary, an electron donating compound are combined therewith to obtain a propylene polymerization catalyst.

The general formula (I) of the organosilicon compound as the component (C) is as follows.

[Chemical 1] (However, R ¹ is a cyclic substituent having an ether bond or a thioether bond in the ring, an oxy group having an in-ring ether bond-containing cyclic substituent, an in-ring ketone bond-containing cyclic substituent, a nitrogen atom-containing heterocyclic substituent. Group, a silicon atom-containing heterocyclic substituent, or a substituent having a lactone skeleton structure, R ² is a hydrocarbon group having 1 to 10 carbon atoms, R ⁴ O—,
R ⁵ ₃ Si- or R ⁶ ₃ SiO- (provided that R ⁴
Is a hydrocarbon group having 3 to 10 carbon atoms, R ⁵ and R ⁶
Are each a hydrocarbon group having 1 to 10 carbon atoms and may be the same or different. ), R ³ is a methyl group or an ethyl group, x is 1 or 2, y is 0 or 1,
z is 2 or 3, and x + y + z = 4. )

(A) Solid component Solid component (hereinafter referred to as component (A)) is magnesium,
Titanium, a halogen and an electron donating compound are essential components, and usually prepared by contacting a magnesium compound, a titanium compound and an electron donating compound (in the case where each of the above compounds does not have a halogen, a halogen containing compound). be able to.

(A) Magnesium compound The magnesium compound is represented by the general formula MgR ⁷ R ⁸ . In the formula, R ⁷ and R ⁸ represent the same or different hydrocarbon groups, OR ′ groups (R ′ is a hydrocarbon group) or halogen atoms. More specifically, as the hydrocarbon of R ⁷ and R ⁸ , an alkyl group having 1 to 20 carbon atoms, a cycloalkyl group,
Examples thereof include an aryl group and an aralkyl group, and examples of the OR ′ group include an alkyl group having a carbon number of 1 to 12 as R ′, a cycloalkyl group, an aryl group and an aralkyl group, and examples of the halogen atom include chlorine, bromine and iodine. , Fluorine and the like.

Specific examples of these compounds are shown below (however, Me: methyl, Et: ethyl, Pr: propyl,
Bu: Butyl, He: Hexyl, Oct: Octyl, P
h: phenyl, cyHe: cyclohexyl. same as below. ). _{MgMe 2, Mg (i-Pr} ) 2, MgB
u ₂ , MgOct ₂ , MgEtBu, MgPh ₂ , Mg
cyHe ₂ , Mg (OEt) ₂ , Mg (OHe) ₂ , M
g (OOct) ₂ , Mg (OPh) ₂ , EtMgCl,
HeMgCl, i-BuMgCl, PhMgCl, Ph
CH ₂ MgCl, BuMgBr, BuMgI, EtOM
gCl, PhOMgCl, EtOMgBr, EtOMg
I, MgCl ₂ , MgBr ₂ , MgI ₂ .

The above-mentioned magnesium compound can be prepared from metallic magnesium or other magnesium compounds when the component (A) is prepared. As an example,
Magnesium metal, halogenated hydrocarbon and general formula: X _n M (OR) _mn (In the formula, X is a hydrogen atom, a halogen atom or a hydrocarbon group having 1 to 20 carbon atoms, and M is boron, carbon or aluminum. , A silicon or phosphorus atom, and R has 1 carbon atom
~ 20 hydrocarbon groups, m is the valency of M,
m> n ≧ 0. The method of contacting the alkoxy group-containing compound of 1) is mentioned.

Hydrocarbons of X and R in the general formula of the alkoxy group-containing compound include methyl (Me), ethyl (E)
t), propyl (Pr), i-propyl (i-Pr),
Butyl (Bu), i-butyl (i-Bu), hexyl (He), octyl (Oct) and other alkyl groups, cyclohexyl (cyHe), methylcyclohexyl and other cycloalkyl groups, allyl, propenyl, butenyl and other alkenyl groups. , Aryl groups such as phenyl (Ph), tolyl, and xylyl groups, aralkyl such as phenethyl, 3-phenylpropyl, and the like. Among these, especially carbon number 1
10 to 10 alkyl groups and the like are desirable.

Specific examples of the alkoxy group-containing compound include C (OEt) ₄ and C (OP) when M is carbon.
r) ₄ , C (OBu) ₄ , C (OOct) ₄ , HC (O
Me) ₃ , HC (OBu) ₃ , HC (OPh) ₃ , Me
C (OEt) ₃ , EtC (OMe) ₃ , PhC (OE
t) ₃ , CH ₂ ClC (OEt) ₃ , MeCHBrC
(OEt) ₃ , ClC (OMe) ₃ , ClC (Oi-B
u) ₃ , BrC (OEt) ₃ , MeCH (OEt) ₂ ,
CH ₂ (OMe) ₂ , CH ₂ ClCH (OEt) ₂ , C
HCl ₂ CH (OEt) ₂ , CCl ₃ CH (OE
t) ₂ , CH ₂ BrCH (OEt) ₂ , PhCH (OE
t) _{2 and the} like, and when M is silicon, Si (O
Et) ₄ , Si (OHe) ₄ , HSi (OEt) ₃ , H
Si (OPh) ₃ , MeSi (OBu) ₃ , PhSi
(OEt) ₃ , CHCl ₂ Si (OEt) ₃ , BrSi
(OEt) ₃ , ClSi (OBu) ₃ , CHCl ₂ Si
H (OEt) ₂ , CCl ₃ SiH (OEt) ₂ , Me ₃
SiOEt _{2 and the} like, and when M is boron, B (OEt) ₃ , B (OBu) ₃ , B (OH
e) ₃ , B (OPh) _{3 and the} like, and when M is aluminum, Al (OMe) ₃ , Al (OEt)
₃ , Al (OHe) ₃ , Al (OPh) _{3 and the} like. Further, when M is phosphorus, P (OMe) ₃ , P
(OEt) ₃ , P (OHe) ₃ , P (OPh) _{3 and the} like can be mentioned.

As the magnesium compound, a metal (M ') of Group II or IIIa of the periodic table represented by the general formula: MgR ⁷ R ⁸ .n (M'R ⁹ _m ).
Complexes with organic compounds of can also be used. The metal M ′ is aluminum, zinc, calcium, etc., and R ⁹ is 1 to 1 carbon atoms.
12 alkyl groups, cycloalkyl groups or aralkyl groups. Further, m represents the valence of the metal M ′, and n is 0.
A number from 1 to 10 is shown. Specific examples of the compound represented by M′R ⁹ _m include AlMe ₃ , AlEt ₃ , and Al (i-B).
u) ₃ , AlPh ₃ , ZnMe ₂ , ZnEt ₂ , ZnB
u ₂ , ZnPh ₂ , CaEt ₂ , CaPh _{2 and the} like can be mentioned.

(B) Titanium compounds Titanium compounds are divalent, trivalent and tetravalent titanium compounds, such as titanium trichloride, titanium tetrachloride, titanium tetrabromide, trichloroethoxytitanium, trichlorobutoxytitanium,
Examples thereof include dichlorodiethoxytitanium, dichlorodibutoxytitanium, dichlorodiphenoxytitanium, chlorotriethoxytitanium, chlorotributoxytitanium and tetrabutoxytitanium. Among these, tetravalent titanium halides such as titanium tetrachloride, trichloroethoxy titanium, dichlorodibutoxy titanium and dichlorodiphenoxy titanium are preferable, and titanium tetrachloride is particularly preferable.

(C) Electron-donating compound Examples of the electron-donating compound include carboxylic acids, carboxylic acid anhydrides, carboxylic acid esters, carboxylic acid halides, alcohols, ethers, ketones, amines and amides. , Nitriles, aldehydes, alcoholates, phosphorus bound to organic groups via carbon or oxygen,
Examples include arsenic or antimony compounds, phosphoamides, thioethers, thioesters, carbonates and the like. Of these, carboxylic acids, carboxylic acid anhydrides, carboxylic acid esters, carboxylic acid halides, alcohols and ethers are preferable.

Specific examples of the carboxylic acid include aliphatic monocarboxylic acids such as formic acid, acetic acid, propionic acid, butyric acid, valeric acid, acrylic acid, methacrylic acid and crotonic acid, malonic acid, succinic acid, adipic acid and maleic acid. Aliphatic dicarboxylic acids such as, tartaric acid and other aliphatic oxycarboxylic acids, cyclohexene monocarboxylic acid, alicyclic carboxylic acids such as cis-1,2-cyclohexanedicarboxylic acid, benzoic acid, toluic acid, anisic acid, cinnamic acid And aromatic polycarboxylic acids such as phthalic acid, naphthalic acid, trimellitic acid, trimesic acid, and mellitic acid. As the carboxylic acid anhydride, the acid anhydrides of the above carboxylic acids can be used.

As the carboxylic acid ester, mono- or polyvalent esters of the above-mentioned carboxylic acids can be used, and specific examples thereof include butyl formate, ethyl acetate, isobutyl pivalate, ethyl acrylate, methyl methacrylate and malon. Diethyl acid salt, dibutyl succinate, diisobutyl adipate, diethyl maleate, diisobutyl maleate, diethyl tartrate, diisobutyl tartrate, ethyl cyclohexanecarboxylate, methyl benzoate, ethyl benzoate, methyl p-toluate, ethyl p-anisate, Ethyl cinnamate, Monomethyl phthalate, Dibutyl phthalate, Diisobutyl phthalate, Diallyl phthalate, Diphenyl phthalate, Diethyl terephthalate, Dibutyl terephthalate, Diethyl naphthalate, Dibutyl naphthalate, Trie trimellitate Le, and the like.

As the carboxylic acid halide, the acid halides of the above carboxylic acids can be used,
Specific examples thereof include acetic acid chloride, acetic acid bromide, acetic acid iodide, propionic acid chloride, butyric acid chloride,
Butyric acid bromide, butyric acid iodide, acrylic acid chloride, acrylic acid bromide, acrylic acid iodide, methacrylic acid chloride, methacrylic acid bromide, methacrylic acid iodide, crotonic acid chloride, malonic acid chloride, malonic acid bromide, succinic acid chloride, succinic acid bromide, Adipic acid chloride, adibic acid bromide,
Maleic acid chloride, maleic acid bromide, tartaric acid chloride, tartaric acid bromide, cyclohexanecarboxylic acid chloride, cyclohexanecarboxylic acid bromide, cis-4-
Methylcyclohexenecarboxylic acid chloride, cis-4-
Methylcyclohexenecarboxylic acid bromide, benzoyl chloride, benzoyl bromide, p-toluyl chloride, p-
Examples thereof include toluic acid bromide, p-anisic acid bromide, p-anisic acid chloride, cinnamic acid bromide, phthalic acid dichloride, phthalic acid dibromide, and naphthalic acid dichloride. Further, a monoalkyl halide of a dicarboxylic acid such as adipic acid monomethyl chloride, maleic acid monoethyl chloride and phthalic acid butyl chloride can also be used.

Alcohols are represented by the general formula R ¹⁰ OH. In the general formula, R ¹⁰ is an alkyl group having 1 to 12 carbon atoms, an alkenyl group, a cycloalkyl group, an aryl group or an aralkyl group. Specific examples include methanol, propanol, isobutanol, pentanol, hexanol, cyclohexanol, benzyl alcohol, allyl alcohol, phenol, cresol, ethylphenol, n-octylphenol group and the like.

The ethers are represented by the general formula R ¹¹ OR ¹² . In the general formula, R ¹¹ and R ¹² are alkyl groups having 1 to 12 carbon atoms, alkenyl groups, cycloalkyl groups, aryl groups or aralkyl groups, which may be the same or different.
Specific examples include diethyl ether, diisopropyl ether, diisoamyl ether, di-2-ethylhexyl ether, diallyl ether, butyl allyl ether, diphenyl ether, anisole group and the like.

(D) Halogen-containing compound Examples of the halogen-containing compound include halogenated hydrocarbons, halogen-containing alcohols, halogenated silicon compounds having a hydrogen-silicon bond, Group IIIa, Group IVa and Va of the periodic table.
Halides of group elements (hereinafter referred to as metal halides)
Etc. can be mentioned.

The halogenated hydrocarbon has 1 to 1 carbon atoms.
Twelve saturated or unsaturated aliphatic, cycloaliphatic and aromatic hydrocarbon mono- and polyhalogen substitutes are mentioned. Specific examples of these compounds include, for aliphatic compounds, methyl chloride, methylene chloride, chloroform, iodoform, carbon tetrachloride, carbon tetraiodide, ethyl bromide, 2-dichloroethane, 1,2-diiodoethane, methyl chloroform, 1,1,2-tribromoethylene,
1,1,2,2-tetrachloroethylene, pentachloroethane, hexachloroethane, hexachloropropylene, decabromobutane, chlorinated paraffin, and the like can be given. Among alicyclic compounds, chlorocyclopropane, hexachlorocyclopentadiene, Hexachlorocyclohexane and the like, aromatic compounds such as chlorobenzene,
Examples thereof include p-dichlorobenzene, hexachlorobenzene, hexabromobenzene, benzotrichloride, p-chlorobenzotrichloride and the like. These compounds may be used alone or in combination of two or more.

As the halogen-containing alcohol, one having one or two or more hydroxyl groups in one molecule, or any one or two or more hydrogen atoms other than hydroxyl groups in the polyhydric alcohol is substituted with a halogen atom. It is a compound. Examples of the halogen atom include chlorine, bromine, iodine and fluorine atoms, and a chlorine atom is particularly desirable. Examples of these compounds include 2-chloroethanol, 1-chloro-2-propanol, 5-chloro-1-pentanol, 3-chloro-1,2-propanediol, 2-chlorocyclohexanol and 4-chlorobenz. Hydrol,
Chlorobenzyl alcohol, 4-chlorocatechol, 4
-Chloro-cresol, chlorohydroquinone, chlorophenol, 6-chlorothymol, 4-chlororesorcin, 2-bromoethanol, 1-bromo-2-butanol, 2-bromo-p-cresol, 1-bromo-2-naphthol, Fluorophenol, p-iodophenol, 2,2-dichloroethanol, 1,3-dichloro-
2-propanol, 2,3-dibromo-1-propanol, 2,4-dibromophenol, 2,2,2-trichloroethanol, 2,3,4-trichlorophenol,
2,4,6-tribromophenol, 2,3,5-tribromo-2-hydroxytoluene, 2,2,2-trifluoroethanol, 2,4,6-triiodophenol, 2,4,3,6 -Tetrafluorophenol, tetrachlorobisphenol A, 2,2,3,3-tetrafluoro-1-propanol, tetrafluororesorcin, and the like.

Examples of the halogenated silicon compound having a hydrogen-silicon bond include HSiCl ₃ , H ₂ SiCl ₂ and H
_{3 SiCl, H (C 2 H} 5) SiCl 2, H (t-C 4
H ₉ ) SiCl ₂ , H (C ₆ H ₅ ) SiCl ₂ , H (C
_{H 3) 2 SiCl, H (} i-C 3 H 7) 2 SiCl, H
_{2 (C 2 H 5) SiCl} , H 2 (n-C 4 H 9) SiC
1, H ₂ (C ₆ H ₄ CH ₃ ) SiCl, H (C ₆ H ₅ ).
₂ SiCl and the like can be mentioned.

As the metal halide, B, Al, Ga,
In, Tl, Si, Ge, Sn, Pb, As, Sb, B
Examples thereof include chloride, fluoride, bromide and iodide of i, and special BCl ₃ , BBr ₃ , BI ₃ , AlCl ₃ and Al.
_{Br 3, GaCl 3, GaBr 3} , InCl 3, TlC
l ₃ , SiCl ₄ , SnCl ₄ , SbCl ₅ , SbF ₅
Etc. are suitable.

A mixture of (a) a magnesium compound, (b) a titanium compound, (c) an electron-donating compound, and optionally (d) a halogen-containing compound in the presence or absence of an inert medium. Or contact by mechanical co-milling. The contact can be performed under heating at 40 to 150 ° C. As the inert medium, saturated aliphatic hydrocarbons such as hexane, heptane and octane, saturated alicyclic hydrocarbons such as cyclopentane and cyclohexane, and aromatic hydrocarbons such as benzene, toluene and xylene can be used.

The component (A) in the present invention is disclosed in JP-A-63-
No. 264607, No. 58-198503, No. 62-1
As disclosed in Japanese Patent No. 46904 and the like, magnesium metal, halogenated hydrocarbons and the general formula X _n M (O
R) A method of contacting a magnesium-containing solid obtained by contacting a compound of _mn (the same as the above-mentioned alkoxy group-containing compound) with a halogen-containing alcohol, and then with an electron-donating compound and a titanium compound (JP-A-63-63) No. 264607), a magnesium dialkoxide and a silicon halide compound having a hydrogen-silicon bond are brought into contact with each other, and then a titanium halide compound is brought into contact therewith, and then an electron donating compound (if necessary, further halogenated). Contacting with a titanium compound (JP-A-62-146904), a magnesium dialkoxide is contacted with a silicon halide compound having a hydrogen-silicon bond, and then with an electron-donating compound, and then a titanium compound. Method of contact with
No. 8-198503) and the like, but the most preferable method is.

The component (A) is prepared as described above, but the component (A) may be washed with the above-mentioned inert medium, if necessary, and further dried.

(B) Organoaluminum Compound Specific examples of the organoaluminum compound (hereinafter referred to as the component (B)) include trimethylaluminum, triethylaluminum, tripropylaluminum, triisopropylaluminum, tributylaluminum, triisobutylaluminum, triisobutylaluminum and triisobutylaluminum. Hexylaluminum and the like can be mentioned.

(C) Organosilicon Compound The organosilicon compound which is a component of the catalyst of the present invention (hereinafter referred to as component (C)) is represented by the above general formula (I).
In the formula, R ¹ is a cyclic substituent having an ether or thioether bond in the ring, an oxy group of a cyclic substituent having an ether bond in the ring, a cyclic substituent having a ketone bond in the ring, a heterocyclic substituent having a nitrogen atom, silicon An atom-containing heterocyclic substituent, a substituent having a lactone skeleton structure, R ² is a hydrocarbon group having 1 to 10 carbon atoms, R ⁴ O-, R ⁵ ₃ Si-
Or R ⁶ ₃ SiO— (provided that R ⁴ is a hydrocarbon group having 3 to 10 carbon atoms, R ⁵ and R ⁶ are each a hydrocarbon group having 1 to 10 carbon atoms), and R ³ is a methyl group or an ethyl group, x is 1 or 2, y is 0 or 1, z is 2 or 3, and x + y + z = 4. Specific examples of R ¹ are shown below (each R ¹ group is represented by RA, RB, ...).

[Chemical 2]

R ² in the above general formula of the component (C),
Examples of the hydrocarbon group in R ⁴ , R ^{5 and} R ⁶ include an alkyl group, an alkenyl group, a cycloalkyl group, a cycloalkenyl group, a cycloalkadienyl group, an aryl group and an aralkyl group. As the alkyl group, ethyl, i
-Propyl, s-butyl, t-butyl, amyl, 2-ethylhexyl, decyl group and the like, and the alkenyl group includes vinyl, allyl, propenyl, 1-hexenyl, 1-octenyl, 1-methyl-1-. Examples thereof include a pentynyl group, examples of the cycloalkyl group include a cyclopentyl group and a methylcyclohexyl group, examples of the cycloalkenyl group include a cyclopentenyl group and cyclohexenyl group, and examples of the cycloalkadienyl group include cyclopentadiene group. Examples of the aryl group include phenyl, tolyl, and a methylcyclopentadienyl group.
Examples thereof include a xylyl group and the like, and examples of the aralkyl group include a benzyl, phenethyl, 1-phenylpropyl group and the like.

Examples of the component (C) are shown below. [RA],
The symbols such as [RB] ... Correspond to the above symbols of R ¹ in the general formula (I) of the component (C). [RA] ₂ Si (OMe) ₂ , [RB] (i-Pr) S
i (OMe) ₂ , [RC] (t-Bu) Si (OMe)
₂ , [RC] (Me ₃ SiO) Si (OMe) ₂ , [R
A] (i-Pr) Si (OEt) ₂ , [RA] Si (O
Me) ₃ , [RD] Si (OMe) ₃ , [RB] Si
(OEt) ₃ , [RE] MeSi (OMe) ₂ , [R
F] (i-PrO) Si (OMe) ₂ , [RG] (i-
Pr) Si (OEt) ₂ , [RH] Si (OMe) ₃ ,
[RI] Si (OEt) ₃ , [RJ] Si (OSiM
e) (OMe) ₂ , [RK] Si (OEt) ₃ , [R
L] Si (OEt) ₃ , [RM] Si (OEt) ₃ ,
[RN] Si (OEt) ₃ .

(D) As the electron donating compound component (D), an electron donating compound composed of an organosilicon compound and an electron donating compound containing a hetero atom such as nitrogen, sulfur, oxygen or phosphorus can be used. However, organosilicon compounds are preferred. The organosilicon compound is preferably one having a total of 4 alkoxy groups (which may be partially substituted with an alkyl group or an aryl group) bonded to a silicon atom. These alkyl groups and alkoxy groups may be chain-like or cyclic. Further, the alkyl group or the aryl group may be substituted with a halogen element.

Such an organosilicon compound (component (D))
Specific examples of tetramethoxysilane, tetraisobutoxysilane, tetraphenoxysilane, tetrabenzyloxysilane, methyltrimethoxysilane, methyltriethoxysilane, methyltriphenoxysilane, ethyltriethoxysilane, butyltriethoxysilane,
Butyltriphenoxysilane, vinyltriethoxysilane, allyltrimethoxysilane, dimethyldiisopropoxysilane, dimethyldiphenoxysilane, diethyldiethoxysilane, diethyldiisobutoxysilane, diethyldiphenoxysilane, dibutyldiisopropoxysilane, dibutyldibutoxysilane Silane, dibutyldiphenoxylan, diisobutyldiethoxysilane, diphenyldimethoxysilane, diphenyldibutoxysilane, dibenzyldiethoxysilane, divinyldiphenoxysilane,
Examples thereof include diallyldipropoxysilane, diphenyldiallyloxysilane, chlorophenyldiethoxysilane and the like.

Specific examples of the electron-donating compound containing a hetero atom include compounds containing a nitrogen atom:
6,6-tetramethylpiperidine, 2,6-diethylpiperidine, 2,6-diisobutyl-4-methylpiperidine, 2,2,5,5-tetramethylpyrrolidine, 3-methylpyridine, 2,6-diisobutylpyridine, 2,5
-Dimethylpiperidine, nicotinic acid amide, imidazole, benzoic acid amide, methyl nicotinate, 2-methylpyrrole, toluic acid amide, benzonitrile, acetonitrile, aniline, toluidine, triethylamine, tetramethylenediamine, tributylamine and the like, and sulfur. As a compound containing an atom, thiophenol,
Thiophene, ethyl 2-thiophenecarboxylate, methyl mercaptan, isopropyl mercaptan, diethyl thioether, diphenyl thioether, methyl benzene sulfonate, methyl sulfite and the like, and as the compound containing an oxygen atom, tetrahydrofuran, 2-methyltetrahydrofuran, 2, 2,5,5-tetraethyltetrahydrofuran, 2,2,6,6-tetramethyltetrahydropyran, dioxane, diethyl ether,
Examples thereof include diphenyl ether, anisole, acetophenone, acetone, o-tolyl-t-butyl ketone, and ethyl 2-furarate. Examples of the compound containing a phosphorus atom include triphenylphosphine, triphenylphosphite, and diethylphosphate.

Two or more kinds of these electron donating compounds may be used. Further, these electron donating compounds may be added when the organoaluminum compound is used in combination with the catalyst component, or may be added after being brought into contact with the organoaluminum compound in advance.

(E) Olefin As olefins, other than ethylene, propylene, 1-
Α such as butene, 1-hexene, 4-methyl-1-pentene
-Olefins can be used.

(Ii) Prepolymerization In the presence of an organoaluminum compound (component (B)) and an organosilicon compound (component (C)), a solid component (component (A)) is contacted with an olefin (component (E)). By doing so, the olefin is prepolymerized. Further, it is preferable to add an electron-donating compound (component (D)) together with the component (B) and the component (C) at the time of prepolymerization, if necessary. The prepolymerization is preferably carried out in the presence of the above-mentioned inert medium. The prepolymerization is usually performed at a temperature of 100 ° C or lower, preferably -30 ° C to +.
It is carried out at a temperature of 30 ° C, more preferably -20 ° C to + 15 ° C. The polymerization method may be a batch method or a continuous method, or may be a multi-step polymerization of two or more steps. When carrying out in multiple stages, it goes without saying that the polymerization conditions can be changed.

Component (B) has a concentration of 10 to 10 in the prepolymerization system.
It is used in an amount of 500 mmol / liter, preferably 30-200 mmol / liter, and is used in an amount of 1-50000 mol, preferably 2-1000 mol, per 1 gram atom of titanium in the component (A). Ingredient (C)
Is used so that the concentration in the prepolymerization system is 5 to 1000 mmol / liter, preferably 10 to 200 mmol / liter. Olefin polymer is incorporated into component (A) by prepolymerization, but the amount of polymer is
(A) 0.1 to 200 g per 1 g, especially 0.5 to 50 g is desirable. The catalyst component of the present invention prepared as described above can be diluted or washed with the above-described inert medium, but it is particularly preferable to wash it from the viewpoint of preventing storage deterioration of the catalyst component. After washing, it may be dried if necessary. Also, when storing the catalyst component,
It is desirable to store at the lowest possible temperature, -50 ℃ to +
A temperature range of 30 ° C, especially -20 ° C to + 5 ° C, is recommended.

(Iii) Main Polymerization The precatalyst component obtained as described above is combined with an organometallic compound and, if necessary, an electron-donating compound, and homopolymerization of propylene or co-polymerization with other monoolefins is carried out. By performing main polymerization such as polymerization, it is possible to obtain a highly crystalline polypropylene in which the relationship between MFR and Nm is represented by the above relational expression.

Organometallic compounds that can be used in the main polymerization are organic compounds of metals of Groups I to III of the periodic table. As the organic metal compound, an organic compound of lithium, magnesium, calcium, zinc or aluminum can be used, and an organic aluminum compound is particularly preferable. Examples of the organoaluminum compound include R ¹³ _n AlX ′ _3-n (wherein R ¹³ is an alkyl group or an aryl group, X ′ is a halogen atom, an alkoxy group or a hydrogen atom, and n is 1 ≦ n ≦ 3. And an alkylaluminum compound such as trialkylaluminum, dialkylaminium monohalide, monoalkylaluminum dihalide, dialkylaluminum monoalkoxide and alkylaluminum monohydride, Alternatively, a mixture or complex compound thereof is particularly preferable. The organoaluminum compound preferably has 1 to 18 carbon atoms, more preferably 2 to 6 carbon atoms.

Specifically, trialkylaluminum such as trimethylaluminum, triethylaluminum, triisobutylaluminum, etc., dialkylaluminum chloride, diethylaluminum bromide, dialkylaluminum monohalide such as diethylaluminium iodide, methylaluminum dichloride, ethylaluminum dibromide. , Monoalkyl aluminum dihalides such as ethyl aluminum diiolide, alkyl aluminum sesquihalides such as methyl aluminum sesquichloride, diethyl aluminum ethoxide,
Examples thereof include dialkyl aluminum monoalkoxides such as diethyl aluminum phenoxide and diisobutyl aluminum ethoxide, and dialkyl aluminum hydrides such as dimethyl aluminum hydride, diethyl aluminum hydride and dipropyl aluminum hydride. Among these, trialkylaluminum is preferable, and triethylaluminum and triisobutylaluminum are particularly preferable.

It is also possible to use an organic alnium compound in which two or more aluminum atoms are bound via an oxygen atom or a nitrogen atom. Examples of such compounds include

[Chemical 3] Etc. can be illustrated.

Examples of organic compounds of metals other than aluminum include diethyl magnesium, ethyl magnesium chloride and diethyl zinc. Further, as an organic compound of aluminum and another metal, LiAl (C
_{2 H 5) 4, LiAl (} C 7 H 15) 4 and the like.

The amount of the organometallic compound used with respect to the pre-catalyst component is usually 1 to 2000 gram moles, preferably 20 to 500 gram moles per 1 gram atom of titanium in the catalyst component. When an electron donating compound is used, the amount of the organometallic compound (as aluminum) is 0.1 to 40 g atom, preferably 1 to 25 g atom per mol of the electron donating compound, so that the amount of the organo metal compound is 1 to 25 g atom. Select the ratio of electron-donating compounds.

The propylene polymerization reaction may be carried out in a gas phase or a liquid phase. When the polymerization is carried out in a liquid phase, normal butane, isobutane, normal pentane, isopentane, hexane, heptane, octane, cyclohexane, benzene, toluene, It can be carried out in an inert hydrocarbon such as xylene and in a liquid monomer. The polymerization temperature is usually -8.
The temperature range is 0 ° C to + 150 ° C, particularly 40 ° C to 120 ° C. The polymerization pressure may be, for example, 1 to 60 atmospheres. Further, the molecular weight of the obtained polymer is controlled by the presence of hydrogen or other known molecular weight regulator. The polymerization reaction is carried out in a continuous or batch reaction, and the conditions may be those normally used. Also, the polymerization reaction may be carried out in one stage or in two stages.

(B) Glass Fiber The glass fiber used in the glass fiber reinforced resin composition of the present invention has an average fiber diameter measured by an electron microscope of 3 to 11 μm.
m. The average fiber length is preferably 0.2 mm or more. The smaller the average fiber diameter of glass fiber,
The glass fiber reinforced resin composition is excellent in mechanical properties such as impact resistance, heat resistance and tensile strength. Considering the surface smoothness of the molded product, chopped strands having a loss on ignition of 0.2 to 0.8% by weight are preferable.

(C) Modified Polyolefin The highly crystalline polypropylene is inferior in chemical properties such as coatability due to its structure, but it can be improved by adding a modified polyolefin. The modified polyolefin is an unsaturated carboxylic acid such as maleic acid or an anhydride thereof,
It is known that it can be obtained by graft-polymerizing an unsaturated carboxylic acid ester such as an acrylic acid ester or a glycidyl compound having an acrylamide group and an epoxy group with a polyolefin as a modifying monomer (see, for example, JP-A-50). -52156, JP-A-52-1
05993, JP-A-55-50040, JP-A-58
-67743, JP-A-6-172422, JP-A-6-
-172460).

The polyolefin graft-polymerized with the modifying monomer is a homopolymer of propylene, a random or block copolymer of propylene, polyethylene, ethylene-propylene rubber, ethylene-butene rubber, polybutylene, ethylene-propylene-diene rubber, propylene-non-conjugated. It is a diene random copolymer or the like and is not particularly limited, but a propylene homopolymer is preferable in view of cost. Examples of the modifying monomer include unsaturated carboxylic acids such as acrylic acid, methacrylic acid, maleic acid, fumaric acid, itaconic acid, 2,3-dicarboxylic acid anhydride, anhydrides thereof or esters thereof, and glycidyl acrylate, glycidyl methacrylate. Unsaturated epoxy compounds such as itaconic acid glycidyl ester are preferred. Furthermore, the following general formula (II):

[Chemical 4] (In the formula, R ¹⁴ is H or an alkyl group having 1 to 6 carbon atoms, Ar is an aromatic hydrocarbon group having 6 to 20 carbon atoms having at least one glycidyloxy group, and n is 1
Represents an integer of 4; A glycidyl compound having an acrylamide group and an epoxy group represented by the formula (1) can also be used as the modifying monomer.

Preferred glycidyl compounds are:
The following general formula (III):

[Chemical 5] (Wherein R ¹⁵ is H or an alkyl group having 1 to 6 carbon atoms). Such a glycidyl compound having an acrylamide group and an epoxy group is disclosed in, for example, JP-A-60-130580. Can be produced by the method shown in No. Of these compounds, maleic anhydride is particularly preferable.

The melt flow rate of the modified polyolefin (MFR, measured at 230 ° C., load 2.16 kg) is 1
It is preferably from 500 g / 10 minutes, particularly from 10 to 200 g / 10 minutes, and the graft ratio is preferably from 0.1 to 10% by weight, particularly from 0.3 to 6.0% by weight.

(D) Other Additives The glass fiber reinforced resin composition of the present invention contains a pigment such as carbon black and titanium oxide, a heat stabilizer, a light stabilizer, a metal activator, and a lubricant depending on the application. And the like can be added within a range that does not impair the object of the present invention.

[2] Mixing ratio The mixing ratio of each component is (a) 20 for highly crystalline polypropylene.
˜97.4% by weight, preferably 48 to 89.5% by weight, and (b) 2.5 to 60% by weight, preferably 10 to 45% by weight of glass fibers having an average fiber diameter of 3 to 11 μm. Yes, (c) 0.1 to 20% by weight of modified polyolefin,
It is preferably 0.5 to 7% by weight.

If the content of the highly crystalline polypropylene is less than 20% by weight, the impact resistance of the resulting glass fiber reinforced resin composition is low, while if it exceeds 97.4% by weight, the impact resistance is lowered. The glass fiber content is 2.5% by weight.
If it is less than 60% by weight, heat resistance and impact resistance are lowered, while if it exceeds 60% by weight, surface workability and productivity are lowered. Further, if the content of the modified polyolefin is less than 0.1% by weight, the effect of addition is not observed, and if it exceeds 20% by weight, the mechanical strength is lowered.

[3] Method for producing glass fiber reinforced resin composition Obtained by melt-kneading the above components with a single-screw extruder, a twin-screw extruder, a Banbury mixer, a kneader or the like in the temperature range of 190 to 280 ° C. You can Alternatively, a masterbatch in which glass fiber is added at a high concentration may be prepared in advance and this may be blended with polypropylene.

[0061]

EXAMPLES The present invention will be described in detail with reference to the following examples and comparative examples, but the present invention is not limited thereto.

Synthesis Example 1 Production of Highly Crystalline Propylene Homopolymer (a) -1 Preparation of Catalyst Component (A) In a 1 liter reaction vessel equipped with a reflux condenser, under a nitrogen gas atmosphere, chip-shaped metallic magnesium ( Purity 99.
5%, 8.3 g of average particle size 1.6 mm) and 250 ml of n-hexane were added, stirred for 1 hour at 68 ° C., metallic magnesium was taken out, and dried under reduced pressure at 65 ° C. to obtain pre-activated metallic magnesium. .

Next, 140 ml of n-butyl ether and an n-butyl ether solution of n-butyl magnesium chloride (1.
(75 mol / l) to a suspension of 0.5 ml
The temperature was maintained at 0 ° C., and a solution of 38.5 ml of n-butyl chloride dissolved in 50 ml of n-butyl ether was added dropwise over 50 minutes. After the reaction was carried out at 70 ° C for 4 hours with stirring, the reaction solution was kept at 25 ° C.

Next, HC (OC ₂ H ₅ ) ₃ was added to this reaction solution.
55.7 ml was added dropwise over 1 hour. 6 after the dropping
The reaction was carried out at 0 ° C. for 15 minutes, the reaction product solid was washed 6 times with 300 ml of n-hexane each time, dried under reduced pressure at room temperature for 1 hour, and a magnesium-containing solid containing magnesium 19.0% and chlorine 28.9% 31. 6 g was recovered.

In a 300 ml reaction vessel equipped with a reflux condenser, a stirrer and a dropping funnel, 6.3 g of magnesium-containing solid and 50 ml of n-heptane under a nitrogen gas atmosphere.
To prepare a suspension and stir at room temperature while stirring 2,2,2-
A mixed solution of 20 ml (0.02 mmol) of trichloroethanol and 11 ml of n-heptane was added from a dropping funnel to 30
The mixture was added dropwise over a period of 1 minute and further stirred at 80 ° C. for 1 hour. The solid obtained was filtered off and 100 ml of n-hexane at room temperature was added.
Was washed 4 times with 100 ml of toluene and then twice with 2 times to obtain a solid component.

40 ml of toluene was added to the above solid component, titanium tetrachloride was further added so that the volume ratio of titanium tetrachloride / toluene was 3/2, and the temperature was raised to 90 ° C. After stirring, a mixed solution of 2 ml of di-n-butyl phthalate and 5 ml of toluene was added dropwise, and then the mixture was stirred at 120 ° C. for 2 hours. The solid substance obtained was filtered off at 90 ° C.
Wash twice with ml at 90 ° C. Furthermore, titanium tetrachloride was newly added so that the volume ratio of titanium tetrachloride / toluene was 3/2, and the mixture was stirred at 120 ° C. for 2 hours, and the mixture was cooled to 100 at room temperature.
5. Catalyst component (A) after washing 7 times with ml of n-hexane 5.
5 g was obtained.

Prepolymerization (adjustment of prepolymerization catalyst component) In a 500 ml reactor equipped with a stirrer, under a nitrogen gas atmosphere, 3.5 g of the component (A) obtained above and 300 ml of n-heptane were put and stirred. While cooling to 5 ° C.
Next, n-heptane solution of triethylaluminum (TEAL) (2.0 mol / liter) and 2,3,4-trimethyl-3-azacyclopentyltrimethoxysilane were added to TEAL and 2,3,4-trimethyl in the reaction system. -3-Azacyclopentyltrimethoxysilane was added so that the concentrations thereof were 100 mmol / liter and 10 mmol / liter, respectively, and the mixture was stirred for 5 minutes.

Then, after depressurizing the system, propylene gas was continuously introduced to polymerize propylene for 2.2 hours. After completion of the polymerization, propylene in the gas phase was purged with nitrogen gas, and the solid phase portion was washed with 100 ml of n-hexane three times at room temperature. Further, the solid phase portion was dried under reduced pressure at room temperature for 1 hour to prepare a prepolymerization catalyst component. As a result of measuring the amount of magnesium contained in the prepolymerization catalyst component, the prepolymerization amount was 1.8 g per 1 g of the component (A).

In a 5-liter stainless steel autoclave equipped with a main polymerization stirrer, 6 ml of a solution of triisobutylaluminum (TiBAL) in n-heptane (0.1 mol / liter) and t-butoxy-t-butyl were placed in a nitrogen gas atmosphere. N-Heptane solution of dimethoxysilane (0.01 mol / liter) 6
What mixed ml and hold | maintained for 5 minutes was added.

Then, hydrogen gas as a molecular weight control agent was added.
After pressurizing 7 liters and 3 liters of liquid propylene, the reaction system was heated to 70 ° C. After charging 38.6 mg of the prepolymerization catalyst component obtained above into the reaction system, propylene was polymerized for 1 hour. After completion of the polymerization, unreacted propylene was purged to obtain 427 g of polypropylene powder. The amount of polypropylene produced per 1 g of the catalyst component (A) was 31.0 kg. The MFR of the obtained polypropylene is 40 g / 10 minutes (230 ° C, load 2.1).
6 kg) and Nm was 184.3.

Synthesis Example 2 Production of Highly Crystalline Propylene Homopolymer (a) -2 Polymerization of propylene was carried out under the same conditions as in Synthesis Example 1 except that the amount of hydrogen gas was 5 liters. Catalyst component (A) 1g
The amount of polypropylene produced per unit was 30.2 kg. The MFR of the obtained polypropylene is 20 g /
10 minutes, Nm was 173.4.

Synthesis Example 3 Production of Modified Polyolefin (c) -1 Propylene Homopolymer 1 with MFR of 0.3 g / 10 min
To 100 parts by weight, 1 part by weight of maleic anhydride and a radical initiator (Nippon Yushi Co., Ltd., Perhexin 2.5B)
0.2 parts by weight was dry blended and melt-kneaded using a 90 mmφ single screw extruder. Pellets were obtained by extruding from a die at a cylinder temperature of 220 ° C. The acid graft ratio of the obtained modified polypropylene was measured by the IR method, and was 0.6.
% By weight. The MFR was 150 g / 10 minutes.

Synthesis Example 4 Production of Modified Polyolefin (c) -2 Propylene Homopolymer 1 with MFR of 0.1 g / 10 min
10 parts by weight of maleic anhydride and a radical initiator (Perhexin 2.5B, manufactured by NOF CORPORATION) with respect to 00 parts by weight
Two parts by weight were dry-blended and melt-kneaded using a 90 mmφ single screw extruder. It was extruded from a die at a cylinder temperature of 200 ° C. to obtain pellets. The acid graft ratio of the modified polypropylene thus obtained was measured by IR method and found to be 5.0% by weight. The MFR was 275 g / 10 minutes.

Synthesis Example 5 Production of Modified Polyolefin (c) -3 Propylene Homopolymer 10 with MFR of 15 g / 10 min
0.2 parts by weight of maleic anhydride and radical initiator (Perhexin 2.5B manufactured by NOF CORPORATION) based on 0 parts by weight
0.15 parts by weight was dry blended and melt-kneaded using a 90 mmφ single screw extruder. It was extruded from a die at a cylinder temperature of 200 ° C. to obtain pellets. As a result of measuring the acid graft ratio of the obtained modified polypropylene by the IR method, the result was 0.
It was 1% by weight. The MFR was 100 g / 10 minutes.

Synthesis Example 6 Production of Modified Polyolefin (c) -4 Propylene homopolymer 100 having MFR of 9 g / 10 min
With respect to parts by weight, the following formula (IV):

[Chemical 6] A glycidyl compound represented by (Kanefuchi Chemical Co., Ltd., AX
E) 1 part by weight and a radical initiator (manufactured by NOF CORPORATION, Perhexin 2.5B) 0.1 part by weight were dry blended and melt-kneaded using a 90 mmφ single screw extruder. It was extruded from a die at a cylinder temperature of 200 ° C. to obtain pellets. As a result of measuring the AXE graft ratio of the obtained modified polypropylene by the IR method, it was 1% by weight. Also, MF
R was 100 g / 10 minutes.

Examples 1 to 7 and Comparative Examples 1 to 11 1. Raw material (a) Polypropylene (a) −1: Highly crystalline propylene homopolymer produced in Synthesis Example 1 MFR: 40 g / 10 min (measured at 230 ° C., load 2.16 kg) Nm (measured by ¹³ C-NMR): 184.3 heat Deformation temperature (℃): 143 (18.6 kg / cm according to ASTM D648
² measurement) Flexural modulus ^{(kgf / cm 2): 22500} ( measured at room temperature by ASTM D790) Izod impact strength (kgf · cm / cm): 2 (ASTM D256
(A) -2: Highly crystalline propylene homopolymer produced in Synthesis Example 2 MFR: 20g / 10min Nm: 173.4 Heat distortion temperature (° C): 143 Flexural modulus (kgf / cm ² ): 22000 Izod impact strength (kgf · cm / cm): 2.5 (a) -3: propylene homopolymer MFR: 15g / 10min Nm: 120.0 thermal deformation temperature (° C.): 125 flexural modulus (kgf / cm ^2): 14500 Izod Impact strength (kgf · cm / cm): 2.5 (b) Glass fiber No. Average fiber diameter (μm) Average fiber length (mm) (b) −1 6.03 (b) −2 9.5 3 (b) −3 13.0 3 (c) Modified polyolefin (modified PO) (c -1: Modified polypropylene MFR produced in Synthesis Example 3: 150 g / 10 min (c) -2: Modified polypropylene MFR produced in Synthesis Example 4: 275 g / 10 min (c) -3: Modified polypropylene produced in Synthesis Example 5 MFR: 100g / 10min (c) -4: Modified polypropylene prepared in Synthesis Example 6 MFR: 100g / 10min

2. Kneading method The raw materials were weighed in the mixing ratios shown in Table 1 and dry-blended with a high-speed mixer, and then 200 at 220 to 250 ° C with a twin-screw extruder (AS20 manufactured by Nakatani Machinery Co., Ltd.).
The mixture was melt-kneaded at a screw rotation speed of rpm and extruded to obtain pellets.

3. Molding method The obtained pellets were heated at a resin temperature of 240 by an injection molding machine.
° C., injection pressure 400 kg / cm ² and at a mold temperature of 50 ° C., to prepare a test piece.

4. Physical property measurement The physical property of each test piece was measured by the following methods. The results are shown in Table 1 below. (1) MFR (g / 10 minutes): Measured according to ASTM D1238 at 230 ° C and a load of 2.16 kg. (2) Tensile strength (kgf / cm ² ): Measured at room temperature according to ASTM D638. (3) Flexural modulus (kgf / cm ² ): Measured at room temperature according to ASTM D790. (4) Bending strength (kgf / cm ² ): Measured at room temperature according to ASTM D790. (5) Heat distortion temperature (℃): 18.6kg / cm ^{2 according} to ASTM D648
Measured by. (6) Izod impact strength (kgf · cm / cm): ASTM D256
Measured at 23 ° C.

[0080]                                   Table 1   Example No.              Example 1    Example 2    Example 3    Example 4  Mixing ratio (wt%)                                                          polypropylene     (a) −1 87 53 ─ 97.4     (a) −2 ─ ─ 65 ─     (a) −3 ─ ─ ─ ─   Glass fiber       (b) −1 ─ ─ ─ ─     (b) −2 10 40 30 2.5     (b) −3 ─ ─ ─ ─   Modified PO       (c) −1 3 7 5 ─     (c) −2 ─ ─ ─ 0.1     (c) −3 ─ ─ ─ ─     (c) −4 ─ ─ ─ ─Physical properties of the composition                                                              MFR 12 9 7 18   Tensile strength 750 1360 1280 580   Flexural modulus 32500 88000 69000 22300   Bending strength 1000 1900 1650 750   Heat distortion temperature 148 157 156 100   Izod 7 12 11 5                             Table 1 (continued)   Example No.              Example 5    Example 6    Example 7    Comparative Example 1    Mixing ratio (wt%)                                                          polypropylene     (a) −1 62 89.5 65 ─     (a) −2 ─ ─ ─ ─     (a) −3 ─ ─ ─ 87   Glass fiber       (b) −1 ─ ─ 30 ─     (b) −2 30 10 ─ 10     (b) −3 ─ ─ ─ ─   Modified PO       (c) −1 ─ ─ 5 3     (c) −2 ─ 0.5 ─ ─     (c) −3 ─ ─ ─ ─     (c) −4 8 ─ ─ ─Physical properties of the composition                                                              MFR 12 14 12 14   Tensile strength 1270 790 1520 690   Flexural modulus 68500 32500 76200 30000   Bending strength 1650 1000 1930 830   Heat distortion temperature 155 148 157 145   Izod 10 7 12 7                             Table 1 (continued)   Example No.              Comparative example 2    Comparative Example 3    Comparative Example 4    Comparative Example 5  Mixing ratio (wt%)   polypropylene     (a) −1 ─ 87 65 70     (a) −2 ─ ─ ─ ─     (a) −3 65 ─ ─ ─   Glass fiber                                                                 (b) −1 ─ ─ ─ ─     (b) −2 30 ─ ─ 30     (b) −3 ─ 10 30 ─   Modified PO                                                                   (c) −1 5 3 5 ─     (c) −2 ─ ─ ─ ─     (c) −3 ─ ─ ─ ─     (c) −4 ─ ─ ─ ─Physical properties of the composition                                                              measured value   MFR 12 15 14 13   Tensile strength 1170 650 1100 520   Flexural modulus 61600 29000 61000 50700   Bending strength 1530 810 1490 670   Heat distortion temperature 154 147 155 136   Izod 9 7 8 4                             Table 1 (continued)   Example No.              Comparative Example 6    Comparative Example 7    Comparative Example 8    Comparative Example 9 Mixing ratio (wt%)                                                    polypropylene                                                       (a) −1 55 ─ ─ ─     (a) −2 ─ ─ ─ ─     (a) −3 − 82 74 46   Glass fiber                                                           (b) −1 ─ ─ ─ ─     (b) −2 20 ─ ─ ─     (b) −3 ─ 10 20 30   Modified PO                                                             (c) −1 25 ─ ─ ─     (c) −2 ─ ─ ─ ─     (c) −3 ─ 8 16 24     (c) −4 ─ ─ ─ ─Physical properties of the composition                                                       measured value                                                                MFR 12 8 8 8   Tensile strength 780 570 800 1000   Flexural modulus 39800 26000 42000 55000   Bending strength 1000 730 1050 1300   Heat distortion temperature 150 135 150 155   Izod 8 5 8 9

As is clear from Table 1, the glass fiber reinforced resin composition of the present invention has excellent mechanical properties even when the glass fiber content is small. As is clear from Example 7 and Comparative Example 4, the smaller the average fiber diameter of the glass fibers, the better the mechanical properties.

The glass fiber reinforced resin composition of the present invention comprises
It is excellent in heat resistance, rigidity, impact resistance, productivity and surface smoothness of molded products, and can be widely used for interior and exterior parts of automobiles, parts for home electric appliances, parts for office equipment and the like.

Front page continuation (72) Inventor Yukihiko Yagi 3-1, Chidori-cho, Kawasaki-ku, Kanagawa Prefecture Tonen Chemical Co., Ltd. Technology Development Center (72) Inventor Toshikazu Honda 3-1, Chidori-cho, Kawasaki-ku, Kawasaki-shi, Kanagawa Tonen Kagaku Co., Ltd. Technical Development Center (72) Inventor Tadashi Sezume 3-1, Chidori-cho, Kawasaki-ku, Kawasaki-shi, Kanagawa Tonen Kagaku Co., Ltd. Technical Development Center (56) Reference JP-A-2-6545 (JP, A) JP 60-90239 (JP, A) JP 2-77459 (JP, A) JP 59-226041 (JP, A) JP 58-104905 (JP, A) JP 64 -66127 (JP, A) JP 61-155404 (JP, A) JP 5-105719 (JP, A) JP 6-184215 (JP, A) (58) Fields investigated (Int.Cl) . ^7, DB name) C08L 23/00 - 23/36 C08K 3/00 - 13/08 C08F 10/00 - 10/14 C08F 110/00 - 110/14 C08F 210/00 - 210/18

Claims (2)

(57) [Claims] 1. A melt flow rate (MFR) of 0.01 to 15 (a) measured according to ASTM D-1238.
It is in the range of 0 g / 10 minutes, and the meso-average chain length (Nm) and MFR determined by ¹³ C-NMR are 20 to 97.4% by weight of a propylene polymer satisfying the relational expression of Nm ≧ 97 + 29.5 log MFR. (b) A glass fiber reinforced resin composition comprising 2.5 to 60% by weight of glass fibers having an average fiber diameter of 3 to 11 μm and (c) 0.1 to 20% by weight of a modified polyolefin. 2. The glass fiber reinforced resin composition according to claim 1, wherein the glass fiber content is 10 to 45% by weight.