JP2009209234A - Resin composition and molded article obtained by molding the same - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a high-performance thermoplastic resin that comprises a polyamide 1010 resin, has high rigidity and high impact resistance, is composed of a plant-derived raw material and has high performance which has not been found in thermoplastic resins for injection molding. <P>SOLUTION: A resin composition comprises a polyamide 1010 resin (A), a fibrous filler (B1) and/or a thermoplastic resin (B2) and has the mass ratio (A/(B1+B2)) of the polyamide 1010 resin (A) to the fibrous filler (B1) and the thermoplastic resin (B2) of 25/75-99/1 and the flexural modulus of the thermoplastic resin (B2) of ≥3.0 GPa. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

  The present invention relates to a high rigidity, high impact resistance environmentally friendly resin composition comprising polyamide 1010 resin.

Conventionally, many resin products are manufactured by injection molding, and various resin materials are used depending on the application. Typical resin materials include polypropylene (PP), acrylonitrile butadiene styrene (ABS), polystyrene (HIPS), polycarbonate / acrylonitrile butadiene styrene (PC / ABS), and the like.
However, these resin materials are manufactured using petroleum, which is difficult to regenerate, and in recent years, mass production and mass consumption of resin products using such petroleum as raw materials are factors that increase global environmental problems such as resource depletion. It has become. Moreover, when incinerated as the final disposal form of resin products, the raw material is petroleum in the ground, so carbon is released to the surface of the earth, leading to global warming problems. Because of these problems, recycling by recycling is being studied, but there are problems such as separation and strength reduction, and the current situation is that it is technically and economically unacceptable.

  In order to solve such environmental problems of petroleum raw material-based resins, use of biomass raw material resins such as renewable plants has begun to be studied. As such a plant-derived resin, a polylactic acid resin, which is a polyester resin, has attracted attention (for example, Patent Document 1). Since polylactic acid resin is a resin made of plant-derived materials, the degree of attention is further increased in order not to increase the total amount of carbon dioxide in the atmosphere even when incinerated.

As with the above-mentioned polyester resins such as polylactic acid, polyamide 11 resins and polyamide 1010 resins are known as polyamide resins produced from plant-derived materials.
Since polyamide 11 resin has both flexibility and durability, it has been suitably used for softeners, automobile-related fluid transport tubes, and the like. However, compared to petroleum-based materials such as ABS and HIPS, polyamide 11 resin is very expensive due to production problems, and this is a factor that hinders the practical spread of polyamide 11 resin-based materials.
Polyamide 1010 resin is also used as a member requiring flexibility in the same way as polyamide 11 resin (for example, Patent Document 2). However, due to its low rigidity, it is deformed at the time of mold release in injection molding. Therefore, it has been difficult to produce an injection molded product using the polyamide 1010 resin.
Japanese Patent Laid-Open No. 06-023828 JP 2006-283781 A

  The present invention provides a thermoplastic resin containing polyamide 1010 resin, having high rigidity and high impact resistance, and having unprecedented high performance among thermoplastic resins for injection molding made of plant-derived raw materials. It is in.

As a result of diligent investigations to solve the above-mentioned problems, the present inventor has greatly improved the mechanical properties of polyamide 11 resin by combining polyamide 1010 resin with a fibrous filler and / or a specific thermoplastic resin. As a result, the present invention has been completed.
That is, the gist of the present invention is as follows.
(1) Polyamide 1010 resin (A), fibrous filler (B1) and / or thermoplastic resin (B2), polyamide 1010 resin (A), fibrous filler (B1), thermoplastic resin A resin composition, wherein the mass ratio (A / (B1 + B2)) of (B2) is 25/75 to 99/1, and the flexural modulus of the thermoplastic resin (B2) is 3.0 GPa or more.
(2) The resin composition according to (1), wherein the fibrous filler (B1) is a glass fiber having a major axis / minor axis of 1.5 to 10 in the fiber cross section.
(3) The resin composition according to (1), wherein the fibrous filler (B1) is at least one plant-derived filler selected from kenaf fiber, bamboo fiber, hemp fiber, and bagasse fiber.
(4) The resin composition according to any one of (1) to (3), wherein the thermoplastic resin (B2) is a polylactic acid resin.
(5) The resin composition according to (4), wherein the polylactic acid resin is crosslinked with a peroxide and / or a (meth) acrylic ester compound.
(6) Further containing a modified polyolefin (C), the content of which is 1 to 100 parts by mass with respect to a total of 100 parts by mass of the polyamide 1010 resin (A), the fibrous filler (B1), and the thermoplastic resin (B2). It is 50 mass parts, The resin composition in any one of (1)-(5) characterized by the above-mentioned.
(7) Further, the layered silicate (D) is contained, and the content is 0 with respect to 100 parts by mass in total of the polyamide 1010 resin (A), the fibrous filler (B1), and the thermoplastic resin (B2). The resin composition according to any one of (1) to (6), wherein the resin composition is 1 to 30 parts by mass.
(8) A molded product obtained by molding the resin composition according to any one of (1) to (7).

  According to the present invention, it is possible to provide a thermoplastic resin composition mainly composed of polyamide 1010 resin which is a plant-derived low environmental load material and excellent in mechanical properties, thermal characteristics and injection moldability. By using this resin composition for various injection-molded products such as automobile parts and parts of electrical products, the use range of polyamide 1010 resin, which is a low environmental load material, can be greatly expanded, and the industrial utility value is extremely high.

The present invention will be specifically described below.
The resin composition of the present invention is a resin composition containing a polyamide 1010 resin (A), a fibrous filler (B1) and / or a thermoplastic resin (B2).

In the present invention, the polyamide 1010 resin (A) is a polycondensate of sebacic acid and decanediamine, and the production method is not particularly limited, and can be produced according to a known method. Moreover, you may use additives, such as various catalysts and a heat stabilizer, in the case of manufacture.
The polyamide 1010 resin (A) used in the present invention preferably has a biomass carbon content of 50% or more measured in accordance with ASTM (D6866) in consideration of environmental load.

In the present invention, as the fibrous filler (B1), carbon fiber, glass fiber, boron fiber, asbestos fiber, polyvinyl alcohol fiber, polyester fiber, acrylic fiber, wholly aromatic polyamide fiber, polybenzoxazole fiber, polytetrafluoro From fibers such as ethylene fiber, kenaf fiber, bamboo fiber, hemp fiber, bagasse fiber, high-strength polyethylene fiber, alumina fiber, silicon carbide fiber, potassium titanate fiber, brass fiber, stainless steel fiber, steel fiber, ceramic fiber, basalt fiber The filler which becomes is mentioned. These fibrous fillers may be used in combination of two or more.
In the present invention, it is preferable to use glass fibers as the fibrous filler (B1), particularly from the viewpoint of performance improvement and availability.
It is also preferable to use plant-derived fillers such as kenaf fiber, bamboo fiber, hemp fiber, bagasse fiber and the like. When a plant-derived filler is used, physical properties can be improved while keeping the degree of biomass of the resin composition high. When these fibrous fillers are used, the impact resistance can be greatly improved compared to the case where the main component is polyamide 11 resin.

In the present invention, various types of glass fibers including those commercially available can be used as the glass fibers, but it is particularly preferable to use glass fibers having a flat cross section. When glass fibers having a flat cross section are used, a large impact resistance improvement effect can be obtained as compared with glass fibers having a normal circular cross section. Examples of the shape of the flat cross section include a gourd type, eyebrows type, oval type, elliptical type, and rectangular shape. The glass fiber having a flat cross section preferably has a major axis / minor axis of 1.5 to 10 and more preferably 2.0 to 6.0. If the major axis / minor axis is less than 1.5, the effect of flattening the cross section is small, and if the major axis / minor axis exceeds 10, it is difficult to produce the glass fiber itself.
The major axis of the fiber cross section is preferably 10 to 50 μm, more preferably 15 to 40 μm, and still more preferably 20 to 35 μm.
Further, the ratio (aspect ratio) of the average fiber length and the average fiber diameter of the glass fibers in the resin composition is preferably 2 to 120, more preferably 2.5 to 70, and 3 to 50. More preferably. If the ratio of the fiber length to the average fiber diameter is less than 2, the effect of improving the mechanical strength is small, and if the ratio of the fiber length to the average fiber diameter exceeds 120, the anisotropy increases and the appearance of the molded product also deteriorates. It becomes like this. In addition, the average fiber diameter of the glass fiber which has a flat cross section means the number average fiber diameter when converting a flat cross section shape into the perfect circle of the same area.
Further, the glass fiber having a flat cross section is a fiber having a general glass fiber composition such as E glass, but any composition can be used as long as the glass fiber can be used, and the glass fiber is particularly limited. is not.
A glass fiber having a flat cross section is produced by a known glass fiber production method, and for improving adhesion to a matrix resin and uniform dispersibility, a silane coupling agent, a titanium coupling agent, a zirconia coupling agent, etc. Are collected by a known sizing agent suitable for a resin containing at least one coupling agent, an antistatic agent, a film forming agent, and the like, and gathered glass fiber strands are collected and cut to a certain length. Used in the form of chopped strands.

In this invention, when using a plant-derived filler as a fibrous filler (B1), it is preferable to use what has been delignified. Those not subjected to delignification may adversely affect the appearance or durability.
As the delignification treatment, a known method may be used as appropriate, but a method using a strong alkali solution such as a sodium hydroxide solution or a potassium hydroxide solution, a method of heating using sodium hydroxide and sodium sulfide, under acidic conditions And a method of treating with molybdate and hydrogen peroxide. In addition, the color development of lignin can be suppressed by further bleaching in addition to the delignification treatment.

  In the present invention, as the thermoplastic resin (B2), a resin having a flexural modulus of 3.0 GPa or more measured according to ASTM (D790) is used. By adding such a resin, the rigidity of the polyamide 1010 resin (A) can be improved without impairing the fluidity. Examples of the thermoplastic resin (B2) include resins such as polystyrene resin, methyl methacrylate / styrene copolymer resin, acrylonitrile / styrene copolymer resin, acrylic resin, polybutylene terephthalate resin, and polylactic acid resin.

In particular, as the polylactic acid resin, those made from various plants such as corn can be used, and in that case, in addition to maintaining fluidity, the degree of plant origin can be kept high. As the polylactic acid resin, poly (L-lactic acid), poly (D-lactic acid), and a mixture or copolymer thereof can be used in terms of heat resistance and moldability.
As the polylactic acid resin, it is preferable to use a polylactic acid resin crosslinked with a peroxide and / or a (meth) acrylic acid ester compound. Thereby, the crystallinity degree at the time of shaping | molding can be improved, and the heat resistance of a molded article can be improved.

  The resin composition of the present invention contains the polyamide 1010 resin (A), a fibrous filler (B1), and / or a thermoplastic resin (B2). The mass ratio (A / (B1 + B2)) of the polyamide 1010 resin (A), the fibrous filler (B1), and the thermoplastic resin (B2) in the resin composition needs to be 25/75 to 99/1. Yes, it is preferably 30/70 to 95/5, and more preferably 35/65 to 90/10. When the content of the fibrous filler (B1) and / or the thermoplastic resin (B2) is less than 1% by mass, the polyamide 1010 resin (A) is not sufficiently modified. Further, when the content of the fibrous filler (B1) and / or the thermoplastic resin (B2) exceeds 75% by mass, when the fibrous filler (B1) is used, the resin component is too small. The mechanical properties are fragile, and the molded body tends to crack when the mold is released during injection molding. On the other hand, when the thermoplastic resin (B2) is used, the properties of the polyamide 1010 resin (A) are impaired, and particularly the impact resistance is lowered.

The resin composition of the present invention preferably contains a modified polyolefin (C). By containing the modified polyolefin, the cost can be reduced while maintaining the physical properties of the polyamide 1010 resin (A). When the polylactic acid resin is contained as the thermoplastic resin (B2), this and the polyamide 1010 resin (A) can be dissolved and impact resistance can be improved.
As the modified polyolefin (C), various modified polyolefins including those commercially available can be used. Among them, due to the magnitude of the impact resistance effect, in particular, copolymers of modified ethylene and / or propylene and α-olefin, and olefins mainly composed of ethylene component and / or propylene component and α, β-unsaturated A copolymer with a carboxylic acid or a derivative thereof, or a graft polymer obtained by grafting an α, β-unsaturated carboxylic acid or a derivative thereof onto the above olefin polymer is preferable. Examples of the unsaturated carboxylic acid that is a modifying component include acrylic acid, methacrylic acid, maleic acid, fumaric acid, itaconic acid, citraconic acid, crotonic acid, and nadic acid (endocisbicyclo [2,2] hept-5- And derivatives thereof include acid halides, esters, amides, imides, anhydrides, and the like, for example, maleyl chloride, maleimide, acrylic acid amide, methacrylic acid amide, Examples thereof include glycidyl methacrylate, maleic anhydride, traconic anhydride, monomethyl maleate, maleic dimethyl, glycidyl maleate and the like. These may be used singly or in combination of two or more. Among these, maleic anhydride is preferable because it has high reactivity and can provide a molded article having good strength and appearance. Specific examples of commercially available modified polyolefins include “Tuffmer” (modified ethylene / α-olefin copolymer) manufactured by Mitsui Chemicals.
The content of the modified polyolefin (C) in the resin composition is 1 to 50 parts by mass with respect to 100 parts by mass in total of the polyamide 1010 resin (A), the fibrous filler (B1), and the thermoplastic resin (B2). It is preferable that it is 3 to 30 parts by mass. If the content of the modified polyolefin (C) is less than 1 part by mass, the effect of improving impact resistance may not be sufficiently obtained. On the other hand, when it exceeds 50 parts by mass, rigidity and heat resistance may be lowered, and the degree of plant origin is also lowered, which is not preferable from the viewpoint of environmental problems.

The resin composition of the present invention preferably contains a layered silicate (D). By containing the layered silicate (D), the mechanical properties of the resin composition can be further improved, and the use application of the resin composition of the present invention can be expanded.
Specific examples of the layered silicate (D) include montmorillonite, layered fluorine mica (synthetic mica), talc, mica, clay, and the like. Of these, montmorillonite and / or layered fluorine mica (synthetic mica) is preferably used from the viewpoint of improving the physical properties of the polyamide resin.
The layered silicate (D) is optimally added during the polymerization of the polyamide 1010 resin (A). If this is difficult, the layered silicate may be added to the quaternary ammonium salt or phosphonium salt before kneading. It is preferable to chemically modify with.
Content of layered silicate (D) in a resin composition is 0.1-30 with respect to a total of 100 mass parts of polyamide 1010 resin (A), fibrous filler (B1), and thermoplastic resin (B2). The amount is preferably part by mass, and more preferably 1 to 15 parts by mass. When the content of the layered silicate (D) is less than 0.1 parts by mass, sufficient effects may not be obtained. When it exceeds 30 parts by mass, adverse effects such as poor fluidity during kneading / molding may occur. There is.

  A pigment, a heat stabilizer, an antioxidant, a weathering agent, a plasticizer, a lubricant, a release agent, an antistatic agent, and the like can be added to the resin composition of the present invention as long as the characteristics are not significantly impaired. Examples of heat stabilizers and antioxidants include hindered phenols, hindered amines, sulfur compounds, copper compounds, alkali metal halides, and the like. In addition, the method of mixing these with the resin composition of this invention is not specifically limited. Moreover, in order to assist flame retardancy in particular, a condensed phosphate ester, polyphosphoric acid, a nitrogen compound flame retardant, or the like may be added.

  The resin composition of the present invention can be formed into various molded products by molding methods such as injection molding, blow molding, extrusion molding, inflation molding, and vacuum molding, pressure molding, and vacuum / pressure molding after sheet processing. In particular, it is preferable to adopt an injection molding method, and in addition to a general injection molding method, gas injection molding, injection press molding, and the like can be employed. As an example of injection molding conditions suitable for the resin composition of the present invention, the cylinder temperature is not less than the melting point or flow start temperature of the resin composition, preferably 190 to 270 ° C., and the mold temperature is that of the resin composition. (Melting point-20 ° C.) or less is appropriate. If the molding temperature is too low, the operability becomes unstable, such as short-circuiting in the molded product, and overload tends to occur. Conversely, if the molding temperature is too high, the resin composition will decompose and the resulting molded product Problems such as reduction in strength and coloration are likely to occur, and both may be undesirable.

  Specific examples of the molded body using the resin composition of the present invention include various parts and casings around a personal computer, cellular phone parts and casings, resin parts for electrical appliances such as OA equipment parts, bumpers, and instrument panels. And resin parts for automobiles such as console boxes, garnishes, door trims, ceilings, floors, and panels around the engine. Moreover, it can also be set as a film, a sheet | seat, a hollow molded product, etc.

Hereinafter, the present invention will be described more specifically with reference to examples. The materials used and the evaluation methods in the examples and comparative examples are as follows.
(1) Materials used

Polyamide resin / Polyamide 1010 resin (A):
100 parts by mass of sebacic acid (manufactured by Toyokuni Oil) was dissolved in hot methanol with stirring. Next, 85 parts by mass of decamethylenediamine (manufactured by Ogura Synthesis Co., Ltd.) was dissolved in methanol and slowly added to the previous methanol solution of sebacic acid. After all the components were added, the mixture was stirred for about 15 minutes, and the precipitate was filtered and washed with methanol to obtain decamethylene diammonium sebacate.
Next, 100 parts by mass of decamethylene diammonium sebacate and 33 parts by mass of water were charged into an autoclave, and after substitution with nitrogen, heating was started while stirring at a preset temperature of 240 ° C. and 25 rpm. After holding at a pressure of 2 MPa for 2 hours, the water vapor was exhausted and the pressure was reduced to normal pressure. The mixture was stirred at normal pressure to 0.02 MPa for 2 to 3 hours, then left to stand for 1 hour and then discharged. Then, it dried under reduced pressure and obtained polyamide 1010 resin.
・ Polyamide 11 resin: Rilsan BECN O TL made by Arkema

Fibrous filler (B1)
Glass fiber A: Nittobo CS3J-451 (glass fiber having a circular cross section of 10 μm in diameter and 3 mm in length)
・ Glass fiber B: CSG3PA820S manufactured by Nittobo Co., Ltd. (flat glass fiber having a flat section with a major axis of 28 μm, a minor axis of 7 μm, and a major / minor axis ratio of 4.0)
-Kenaf fiber:
The kenaf cut into a fixed length of about 5 mm was pulverized and loosened with a turbo mill (T-250 manufactured by Matsubo) to give a diameter of 20 to 50 μm and a fiber length of 1 to 5 mm. This was subjected to pressure and heat treatment using a sodium hydroxide solution to remove lignin.

Thermoplastic resin / polylactic acid resin A: Terramac TE-4000 manufactured by Unitika (flexural modulus: 3.7 GPa)
-Polylactic acid resin B:
Using a twin screw extruder (TEM37BS type manufactured by Toshiba Machine), 100 parts by mass of polylactic acid resin A is supplied from the root supply port of the extruder, under conditions of barrel temperature 180 ° C., screw rotation speed 280 rpm, discharge 15 kg / h. The extrusion was carried out while venting. Furthermore, 0.1 part by mass of ethylene glycol dimethacrylate and 0.2 part by mass of a peroxide (Nippon Yushi Co., Ltd., Perbutyl D) were supplied into the cylinder. The resin discharged from the tip of the extruder was cut into pellets to obtain pellets of the resin composition. The obtained pellet was vacuum-dried at 70 ° C. for 24 hours to obtain a crosslinked polylactic acid resin B (flexural modulus: 4.2 GPa).
Polystyrene resin: Nippon Polystyrene G440K (flexural modulus: 3.2 GPa)
Polypropylene resin: Nippon Polypro Novatec PP MA3 (flexural modulus: 1.5 GPa)

-Modified polyolefin (C): Made by Mitsui Chemicals Modified ethylene / α-olefin copolymer TAFMER MH5030
・ Layered silicate (D): SHOEN W manufactured by Hojun

(2) Evaluation method (A) Flexural modulus: measured in accordance with ASTM D790.
(B) Izod impact value: Measured according to ASTM D256-56.
(C) Deflection temperature under load: Based on ASTM D648, the heat distortion temperature was measured at a load of 1.8 MPa.
(D) Fluidity:
According to the measurement method by bar flow. That is, using a spiral mold having a width of 20 mm and a thickness of 2 mm, injection molding was performed at a resin temperature of 220 ° C., a mold temperature of 50 ° C., and an injection pressure of 100 MPa, and the flow length was measured. In the case of 400 mm or more, the evaluation was ○, in the case of 200 mm or more and less than 400 mm, Δ, and in the case of less than 200 mm, ×
(E) Presence or absence of deformation:
An ASTM bending test piece was injection molded under the conditions of a resin temperature of 220 ° C., a mold temperature of 50 ° C., an injection pressure of 100 MPa, and a cooling time of 15 s, and the presence or absence of deformation of the test piece by the ejector pin at the time of mold release was examined.

Examples 1-13, Comparative Examples 2-4, 6, 7
Using a twin-screw extruder (TEM37BS type manufactured by Toshiba Machine), polyamide resin, kenaf fiber, thermoplastic resin, modified polyolefin, and layered silicate are dry blended in the parts by mass shown in Table 1, and from the root supply port of the extruder Then, glass fiber is supplied from the side supply port of the extruder in the mass part shown in Table 1, and extruded while venting under the conditions of a barrel temperature of 240 ° C., a screw rotation speed of 230 rpm, and a discharge of 15 kg / h. Carried out. The resin discharged from the tip of the extruder was cut into pellets to obtain pellets of the resin composition.
The obtained pellets were vacuum-dried at 80 ° C. for 24 hours, and then a test piece for measuring general physical properties while adjusting the mold surface temperature to 50 ° C. using an injection molding machine (Robot Shot S-2000i type manufactured by FANUC). (ASTM type) and bar flow test pieces were prepared and subjected to various measurements.

Comparative Examples 1 and 5
Polyamide 1010 resin (A) or polyamide 11 resin using an injection molding machine (FANUC ROBOSHOT S-2000i type) while adjusting the mold surface temperature to 50 ° C., test piece for general physical properties measurement (ASTM type) And bar flow test pieces were prepared and subjected to various measurements.

As can be seen from Table 1, in the examples, resin compositions having high rigidity, excellent heat resistance, and no deformation at the time of mold release in injection molding were obtained.
In Example 2, a molded body having improved impact resistance as compared with Example 1 was obtained by using glass fiber B having a flat cross section as the glass fiber. Moreover, in Example 8, 9, 11-13, the molded object excellent in heat resistance compared with the case where the polylactic acid resin A was used by using the polylactic acid resin B bridge | crosslinked as a polylactic acid resin. Obtained. In Examples 12 and 13, since the modified polyolefin (C) was blended, a molded article having extremely excellent impact resistance was obtained. In particular, in Example 13, by using the layered silicate (D), a molded article having improved various physical properties was obtained.
On the other hand, in the comparative example 1, since it is the polyamide 1010 resin single-piece | unit, it was too flexible for injection molding, and it was difficult to release.
In Comparative Example 2, since the flexural modulus of the thermoplastic resin used was not 3.0 GPa or more, no improvement in flexural modulus was observed in the obtained resin composition.
Moreover, in Comparative Example 3, since the content of the fibrous filler (B1) was too large, the resulting resin composition became brittle, and the molded body was damaged during mold release. Furthermore, the fluidity was poor. In Comparative Example 4, since the content of the thermoplastic resin (B2) was too much, the heat resistance and impact resistance were reduced.
In Comparative Example 5 using the polyamide 11 resin alone, as in Comparative Example 1, it was difficult to release the mold. Moreover, even if glass fiber or polylactic acid resin is added to this (Comparative Examples 6 and 7), the improvement in impact resistance as seen in the case of adding to the polyamide 1010 resin (Examples 2 and 11) is Not. This shows that a specific effect appears in the combination of polyamide 1010 resin and glass fiber.

Claims (8)

Polyamide 1010 resin (A), fibrous filler (B1) and / or thermoplastic resin (B2), polyamide 1010 resin (A), fibrous filler (B1), thermoplastic resin (B2) The mass ratio (A / (B1 + B2)) is 25/75 to 99/1, and the flexural modulus of the thermoplastic resin (B2) is 3.0 GPa or more. The resin composition according to claim 1, wherein the fibrous filler (B1) is a glass fiber having a major axis / minor axis of 1.5 to 10 in the fiber cross section. The resin composition according to claim 1, wherein the fibrous filler (B1) is at least one plant-derived filler selected from kenaf fibers, bamboo fibers, hemp fibers, and bagasse fibers. The resin composition according to any one of claims 1 to 3, wherein the thermoplastic resin (B2) is a polylactic acid resin. The resin composition according to claim 4, wherein the polylactic acid resin is crosslinked with a peroxide and / or a (meth) acrylic acid ester compound. Furthermore, the modified polyolefin (C) is contained, and the content thereof is 1 to 50 parts by mass with respect to 100 parts by mass in total of the polyamide 1010 resin (A), the fibrous filler (B1), and the thermoplastic resin (B2). The resin composition according to any one of claims 1 to 5, wherein: Furthermore, it contains layered silicate (D), and the content thereof is 0.1 to 0.1 parts by mass with respect to 100 parts by mass in total of polyamide 1010 resin (A), fibrous filler (B1), and thermoplastic resin (B2). It is 30 mass parts, The resin composition in any one of Claims 1-6 characterized by the above-mentioned. The molded object formed by shape | molding the resin composition in any one of Claims 1-7.