JPH07102153A - Resin composition - Google Patents
Resin compositionInfo
- Publication number
- JPH07102153A JPH07102153A JP27760493A JP27760493A JPH07102153A JP H07102153 A JPH07102153 A JP H07102153A JP 27760493 A JP27760493 A JP 27760493A JP 27760493 A JP27760493 A JP 27760493A JP H07102153 A JPH07102153 A JP H07102153A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- resin composition
- coupling agent
- epoxy resin
- parts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000011342 resin composition Substances 0.000 title claims abstract description 19
- 239000003822 epoxy resin Substances 0.000 claims abstract description 15
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 15
- 239000011256 inorganic filler Substances 0.000 claims abstract description 12
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 12
- 239000006087 Silane Coupling Agent Substances 0.000 claims abstract description 11
- 229920006230 thermoplastic polyester resin Polymers 0.000 claims abstract description 7
- 238000013329 compounding Methods 0.000 abstract description 5
- 239000002131 composite material Substances 0.000 abstract description 3
- 239000003365 glass fiber Substances 0.000 abstract description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 abstract description 2
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 abstract description 2
- 239000000843 powder Substances 0.000 abstract description 2
- 239000010453 quartz Substances 0.000 abstract description 2
- 229910000077 silane Inorganic materials 0.000 abstract description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 2
- 229920000728 polyester Polymers 0.000 abstract 1
- 229920001169 thermoplastic Polymers 0.000 abstract 1
- 239000004416 thermosoftening plastic Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 238000005259 measurement Methods 0.000 description 9
- 230000000704 physical effect Effects 0.000 description 9
- -1 polyethylene terephthalate Polymers 0.000 description 9
- OJMOMXZKOWKUTA-UHFFFAOYSA-N aluminum;borate Chemical compound [Al+3].[O-]B([O-])[O-] OJMOMXZKOWKUTA-UHFFFAOYSA-N 0.000 description 7
- 238000002156 mixing Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000008188 pellet Substances 0.000 description 6
- 229920001707 polybutylene terephthalate Polymers 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 239000007822 coupling agent Substances 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 229920003986 novolac Polymers 0.000 description 2
- 239000004843 novolac epoxy resin Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 1
- VJAVYPBHLPJLSN-UHFFFAOYSA-N 3-dimethoxysilylpropan-1-amine Chemical compound CO[SiH](OC)CCCN VJAVYPBHLPJLSN-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 239000004420 Iupilon Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- OTARVPUIYXHRRB-UHFFFAOYSA-N diethoxy-methyl-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](C)(OCC)CCCOCC1CO1 OTARVPUIYXHRRB-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- KBJFYLLAMSZSOG-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)aniline Chemical compound CO[Si](OC)(OC)CCCNC1=CC=CC=C1 KBJFYLLAMSZSOG-UHFFFAOYSA-N 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000000326 ultraviolet stabilizing agent Substances 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Epoxy Resins (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、耐衝撃強度及び靱性に
優れた樹脂組成物に関するものであり、自動車、家電製
品、電子部品などの機能性複合材料として有用である。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resin composition having excellent impact strength and toughness, which is useful as a functional composite material for automobiles, home electric appliances, electronic parts and the like.
【0002】[0002]
【従来の技術】従来、樹脂の強度、弾性率等の機械的な
物性を向上させるため、一種もしくは二種以上の繊維状
または粒子状の充填剤を添加している。また、樹脂と充
填剤間の密着性を改善するために、カップリング剤で充
填剤の表面改質を行うか、あるいはカップリング剤を直
接樹脂と混合している。特公昭48−6175号公報に
はポリエステル系樹脂の強度を改善する目的で、エポキ
シ樹脂を添加した樹脂組成物が、さらに、特開昭64−
29456号公報には、ポリエチレンテレフタレート樹
脂にエポキシ化合物及びガラス繊維を添加して、成形性
を改善した樹脂組成物がそれぞれ開示されている。2. Description of the Related Art Conventionally, in order to improve mechanical properties such as strength and elastic modulus of resin, one or more kinds of fibrous or particulate fillers are added. Further, in order to improve the adhesion between the resin and the filler, the surface of the filler is modified with a coupling agent, or the coupling agent is directly mixed with the resin. Japanese Patent Publication No. 48-6175 discloses a resin composition to which an epoxy resin is added for the purpose of improving the strength of a polyester resin.
Japanese Patent Publication No. 29456 discloses a resin composition in which a moldability is improved by adding an epoxy compound and glass fiber to a polyethylene terephthalate resin.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、前記の
樹脂組成物によれば、引張強度、曲げ強度、衝撃強度が
向上するものの、引張伸度は低下するという問題があ
り、機械的な特性向上には未だ満足しうる状態に至って
いない。本発明の目的は、引張強度、曲げ強度、衝撃強
度及び引張伸度のいずれの特性も向上させ、且つ高い靱
性を有する樹脂組成物を提供することにある。However, according to the above resin composition, although the tensile strength, the bending strength and the impact strength are improved, there is a problem that the tensile elongation is lowered, and the mechanical properties are improved. Is not yet in a satisfactory state. An object of the present invention is to provide a resin composition having improved properties such as tensile strength, bending strength, impact strength and tensile elongation and having high toughness.
【0004】[0004]
【課題を解決するための手段】本発明者等は、このよう
な事情に鑑み鋭意研究を重ねた結果、熱可塑性ポリエス
テル樹脂にエポキシ樹脂とシランカップリング剤及び無
機質充填剤を配合させることにより、エポキシ樹脂とシ
ランカップリング剤が熱可塑性ポリエステル樹脂と無機
質充填剤の密着性を向上させることを見出し、本発明を
完遂するに至った。Means for Solving the Problems The inventors of the present invention have made extensive studies in view of such circumstances, and as a result, by blending an epoxy resin, a silane coupling agent and an inorganic filler with a thermoplastic polyester resin, The present inventors have found that an epoxy resin and a silane coupling agent improve the adhesiveness between a thermoplastic polyester resin and an inorganic filler, and have completed the present invention.
【0005】本発明樹脂組成物の典型的な配合比は、熱
可塑性ポリエステル樹脂38〜94重量部、エポキシ樹
脂0.5〜5.0重量部、シランカップリング剤0.5
〜2.0重量部、無機質充填剤5.0〜60重量部であ
り、これらの配合比は、樹脂の種類及び分子量、無機質
充填剤の種類などによって異なる。また、本発明の実施
においては、樹脂組成物の性能を損なわない程度であれ
ば樹脂及び無機質充填剤を二種類以上混合しても差し支
えない。A typical compounding ratio of the resin composition of the present invention is as follows: thermoplastic polyester resin 38 to 94 parts by weight, epoxy resin 0.5 to 5.0 parts by weight, silane coupling agent 0.5.
To 2.0 parts by weight, and the inorganic filler is 5.0 to 60 parts by weight, and the compounding ratio of these varies depending on the type and molecular weight of the resin, the type of the inorganic filler, and the like. Further, in the practice of the present invention, two or more kinds of resin and inorganic filler may be mixed as long as the performance of the resin composition is not impaired.
【0006】本発明の樹脂組成物に使用されるエポキシ
樹脂としては、ビスフェノール型あるいはノボラック型
のいずれでも良いが、ガラス転移点の高いノボラック型
の方が好ましい。また、ウェルド強度をより向上させた
い場合、結晶化速度の遅い脂環式エポキシ樹脂が望まし
い。The epoxy resin used in the resin composition of the present invention may be either a bisphenol type or a novolac type, but a novolac type having a high glass transition point is preferable. Further, in order to further improve the weld strength, an alicyclic epoxy resin having a slow crystallization rate is desirable.
【0007】本発明の樹脂組成物に使用される無機質充
填剤としては、ガラス繊維、炭素繊維、金属繊維、チタ
ン酸カリウム、炭化ケイ素、タルク、ウオラストナイ
ト、窒化ケイ素、ホウ酸アルミニウム、ホウ酸マグネシ
ウム等のセラミック繊維や石英粉などが好適である。The inorganic filler used in the resin composition of the present invention includes glass fiber, carbon fiber, metal fiber, potassium titanate, silicon carbide, talc, wollastonite, silicon nitride, aluminum borate, boric acid. Ceramic fibers such as magnesium and quartz powder are suitable.
【0008】本発明の樹脂組成物に使用されるシランカ
ップリング剤としては、ビニルトリス(βメトキシ)シ
ラン、ビニルトリエトキシシラン、ビニルトリメトキシ
シラン、γ−メタクリロキシプロピルトリメトキシシラ
ン、γ−グリシドキシプロピルトリメトキシシラン、γ
−グリシドキシプロピルメチルジエトキシシラン、N−
β(アミノエチル)γ−アミノプロピルトリメトキシシ
ラン、N−β(アミノエチル)γ−アミノプロピルジメ
トキシシラン、γ−アミノプロピルトリエトキシシラ
ン、N−フェニル−γ−アミノプロピルトリメトキシシ
ラン等が用いられる。The silane coupling agent used in the resin composition of the present invention includes vinyltris (βmethoxy) silane, vinyltriethoxysilane, vinyltrimethoxysilane, γ-methacryloxypropyltrimethoxysilane and γ-glycid. Xypropyltrimethoxysilane, γ
-Glycidoxypropylmethyldiethoxysilane, N-
β (aminoethyl) γ-aminopropyltrimethoxysilane, N-β (aminoethyl) γ-aminopropyldimethoxysilane, γ-aminopropyltriethoxysilane, N-phenyl-γ-aminopropyltrimethoxysilane and the like are used. .
【0009】本発明の樹脂組成物の製造において、熱可
塑性ポリエステル樹脂及び無機質充填剤の混合物にシラ
ンカップリング剤及び溶剤を用いて液状化あるいは固体
樹脂を粉砕したエポキシ樹脂を添加して混合する。投入
時の順序及び混合方法等については特に限定されず、無
機質充填剤が予めシランカップリング剤で表面処理が施
されている場合には、エポキシ樹脂を添加するだけでも
差し支えない。このようにして得られた混合物は、80
〜140℃の温度で約5時間乾燥したのち、押出機等を
用いて樹脂に適した温度で混練溶融押出しを行ってペレ
ット状に成形される。In the production of the resin composition of the present invention, an epoxy resin obtained by liquefying or crushing a solid resin using a silane coupling agent and a solvent is added to a mixture of a thermoplastic polyester resin and an inorganic filler and mixed. The order and mixing method at the time of charging are not particularly limited, and when the inorganic filler has been surface-treated with a silane coupling agent in advance, addition of an epoxy resin is sufficient. The mixture thus obtained is 80
After drying at a temperature of ˜140 ° C. for about 5 hours, it is kneaded and melt-extruded at a temperature suitable for the resin using an extruder or the like to form a pellet.
【0010】また、本発明の樹脂組成物には、本発明の
目的を逸脱しない範囲で少量の離型剤、着色剤、耐熱安
定剤、紫外線安定剤、発泡剤、難燃剤、難燃助剤、防錆
剤、帯電防止剤等の添加剤を含有させても差し支えな
い。In the resin composition of the present invention, a small amount of a releasing agent, a colorant, a heat stabilizer, an ultraviolet stabilizer, a foaming agent, a flame retardant, a flame retardant auxiliary agent is used within the range not departing from the object of the present invention. Additives such as rust preventives and antistatic agents may be included.
【0011】次に、本発明を実施例により具体的に説明
するが、本発明はこれらの実施例のみに限定されるもの
ではない。Next, the present invention will be specifically described by way of examples, but the present invention is not limited to these examples.
【0012】[0012]
(実施例1)ポリブチレンテレフタレート〔商品名:プ
ラナックBT−1030、大日本インキ化学工業(株)
製〕を69.5重量部に対して、ノボラックエポキシ樹
脂〔商品名:DEN431、ダウ・ケミカル製〕を0.
5重量部を添加混合し、この混合物を120℃で5時間
乾燥したのち、二軸押出機〔商品名:TEM−35B、
東芝機械(株)製〕を用いて温度240℃、回転速度2
00rpmで混練し、この混練物に予めγ−アミノプロ
ピルトリメトキシシランカップリング剤〔商品名:KB
E903、信越化学工業(株)製〕で表面処理した繊維
径0.5〜1.0μm、繊維長10〜20μmのホウ酸
アルミニウムウィスカー〔商品名:アルボレックスYS
3A、四国化成工業(株)製〕30重量部をサイドフィ
ーダから投入し、溶融押出しを行ってペレット状とし
た。このようにして得られたペレットを120℃の温度
で5時間乾燥し、射出成形により試験片を作製してその
物性試験を行ったところ、これらの測定結果は表1に示
すとおりであった。(Example 1) Polybutylene terephthalate [Brand name: Planac BT-1030, Dainippon Ink and Chemicals, Inc.]
69.5 parts by weight of novolac epoxy resin [trade name: DEN431, manufactured by Dow Chemical].
After adding and mixing 5 parts by weight and drying the mixture at 120 ° C. for 5 hours, a twin-screw extruder [trade name: TEM-35B,
Manufactured by Toshiba Machine Co., Ltd.] with a temperature of 240 ° C. and a rotation speed of 2
The mixture was kneaded at 00 rpm, and the kneaded product was previously mixed with a γ-aminopropyltrimethoxysilane coupling agent [trade name: KB
E903, manufactured by Shin-Etsu Chemical Co., Ltd.] surface-treated with aluminum borate whiskers having a fiber diameter of 0.5 to 1.0 μm and a fiber length of 10 to 20 μm (trade name: Arbolex YS)
3A, manufactured by Shikoku Chemicals Co., Ltd.] 30 parts by weight was charged from a side feeder and melt-extruded to obtain pellets. The pellets thus obtained were dried at a temperature of 120 ° C. for 5 hours, a test piece was prepared by injection molding, and the physical properties of the test piece were tested. The results of these measurements are shown in Table 1.
【0013】(実施例2)表面処理を施していないホウ
酸アルミニウムウィスカー〔商品名:アルボレックス
Y、四国化成工業(株)製〕を用いて、γ−アミノプロ
ピルトリメトキシシランカップリング剤〔商品名:KB
E903、信越化学工業(株)製〕を後から添加した以
外は実施例1と同じ原料を用い、表1に示した配合比率
で混合し、実施例1と同じ方法でペレット化し、且つこ
れを同様に処理して試験片を作製して物性試験を行った
ところ、これらの測定結果は表1に示すとおりであっ
た。(Example 2) Using an aluminum borate whisker (trade name: Arbolex Y, manufactured by Shikoku Chemicals Co., Ltd.) which has not been surface-treated, a γ-aminopropyltrimethoxysilane coupling agent [commodity] Name: KB
E903, manufactured by Shin-Etsu Chemical Co., Ltd.] was added later, the same raw materials as in Example 1 were used, mixed in the mixing ratio shown in Table 1, pelletized in the same manner as in Example 1, and When the same treatment was performed to prepare a test piece and a physical property test was performed, these measurement results were as shown in Table 1.
【0014】(比較例1)実施例2において使用したの
と同じポリブチレンテレフタレート69.5重量部、ホ
ウ酸アルミニウムウィスカー30重量部及びノボラック
エポキシ樹脂0.5重量部を用いて、実施例1と同じ方
法でペレット化し、且つこれを同様に処理して試験片を
作製して物性試験を行ったところ、これらの測定結果は
表1に示すとおりであった。Comparative Example 1 Using the same polybutylene terephthalate 69.5 parts by weight as used in Example 2, 30 parts by weight of aluminum borate whiskers and 0.5 parts by weight of novolac epoxy resin, the same procedures as in Example 1 were carried out. Pellets were formed by the same method and treated in the same manner to prepare test pieces, and the physical properties were tested. The results of these measurements are shown in Table 1.
【0015】(比較例2)実施例1において使用したの
と同じポリブチレンテレフタレート70重量部、ホウ酸
アルミニウムウィスカー30重量部を用いて実施例1と
同じ方法でペレット化し、且つこれを同様に処理して試
験片を作製して物性試験を行ったところ、これらの測定
結果は表1に示すとおりであった。Comparative Example 2 Pelletization was carried out in the same manner as in Example 1 using 70 parts by weight of the same polybutylene terephthalate and 30 parts by weight of aluminum borate whiskers used in Example 1, and the same treatment was carried out. Then, a test piece was prepared and a physical property test was conducted, and the measurement results were as shown in Table 1.
【0016】[0016]
【表1】 [Table 1]
【0017】(実施例3)熱可塑性ポリエステル樹脂と
して、ポリブチレンテレフタレート〔商品名:プラナッ
クBT−1030、大日本インキ化学工業(株)製〕2
0.5重量部とポリカーボネート〔商品名:ユーピロン
E2000F、三菱ガス化学(株)製〕49.0重量部
を配合したものを用いた以外は、実施例1において使用
したのと同じ原料を用い、表2に示す配合比率で混合
し、実施例1と同じ方法でペレット化し、且つこれを同
様に処理して試験片を作製して物性試験を行ったとこ
ろ、これらの測定結果は表2に示すとおりであった。(Example 3) As a thermoplastic polyester resin, polybutylene terephthalate [trade name: PLANAC BT-1030, manufactured by Dainippon Ink and Chemicals, Inc.] 2
Using the same raw materials as used in Example 1, except that a mixture of 0.5 parts by weight and 49.0 parts by weight of polycarbonate [trade name: Iupilon E2000F, manufactured by Mitsubishi Gas Chemical Co., Inc.] was used, The mixture was mixed in the mixing ratio shown in Table 2, pelletized by the same method as in Example 1, and treated in the same manner to prepare a test piece, and a physical property test was conducted. The measurement results are shown in Table 2. It was as it was.
【0018】(実施例4)実施例3においてエポキシ樹
脂を脂環式エポキシ樹脂〔商品名:セロキサイト202
1、ダイセル化学工業(株)製〕に代えた以外は、実施
例3において使用したのと同じ原料を用い、表2に示す
配合比率で混合し、実施例1と同じ方法でペレット化
し、且つこれを同様に処理して試験片を作製して物性試
験を行ったところ、これらの測定結果は表2に示すとお
りであった。Example 4 The epoxy resin used in Example 3 was replaced with an alicyclic epoxy resin [trade name: Celoxite 202].
1, manufactured by Daicel Chemical Industries, Ltd.] except that the same raw materials as those used in Example 3 were used, mixed at the compounding ratio shown in Table 2, pelletized in the same manner as in Example 1, and When this was treated in the same manner to prepare a test piece and a physical property test was conducted, these measurement results were as shown in Table 2.
【0019】(比較例3)実施例3において使用したの
と同じポリブチレンテレフタレート21重量部、ポリカ
ーボネート49.0重量部及びホウ酸アルミニウムウィ
スカー30重量部を用いて、実施例1と同じ方法でペレ
ット化し、且つこれを同様に処理して試験片を作製して
物性試験を行ったところ、これらの測定結果は表2に示
すとおりであった。Comparative Example 3 Pellets were prepared in the same manner as in Example 1 using 21 parts by weight of the same polybutylene terephthalate as used in Example 3, 49.0 parts by weight of polycarbonate and 30 parts by weight of aluminum borate whiskers. Then, a test piece was prepared by subjecting it to the same treatment as above, and a physical property test was conducted. The results of these measurements were as shown in Table 2.
【0020】[0020]
【表2】 [Table 2]
【0021】(実施例5)実施例1においてポリブチレ
ンテレフタレートをポリエチレンテレフタレート(固有
粘度0.67)に代えた以外は、実施例1において使用
したのと同じ原料を用い、表3に示す配合比率で混合
し、実施例1と同じ方法でペレット化し、且つこれを同
様に処理して試験片を作製して物性試験を行ったとこ
ろ、これらの測定結果は表3に示すとおりであった。Example 5 The same raw materials as those used in Example 1 were used except that polybutylene terephthalate was replaced with polyethylene terephthalate (intrinsic viscosity 0.67) in Example 1, and the mixing ratio shown in Table 3 was used. Were mixed, pelletized by the same method as in Example 1, and treated in the same manner to prepare a test piece, and a physical property test was conducted. The measurement results are shown in Table 3.
【0022】(比較例4)実施例5において使用したの
と同じポリエチレンテレフタレート70重量部及び実施
例2において使用したのと同じホウ酸アルミニウムウィ
スカー30重量部を用い、実施例1と同じ方法でペレッ
ト化し、且つこれを同様に処理して試験片を作製して物
性試験を行ったところ、これらの測定結果は表3に示す
とおりであった。Comparative Example 4 Pellets were prepared in the same manner as in Example 1 using 70 parts by weight of the same polyethylene terephthalate used in Example 5 and 30 parts by weight of the same aluminum borate whiskers used in Example 2. Then, this was treated in the same manner and a test piece was prepared and a physical property test was conducted. The results of these measurements were as shown in Table 3.
【0023】[0023]
【表3】 [Table 3]
【0024】[0024]
【発明の効果】実施例の結果から、本発明の樹脂組成物
は、エポキシ樹脂とシランカップリング剤を併用して改
質された無機質充填剤を配合しているので、シランカッ
プリング剤あるいはエポキシ樹脂を単独で用いた樹脂組
成物と比較して、引張強度、引張伸度、曲げ強度、曲げ
弾性率、アイゾット衝撃強度などの機械的な特性が飛躍
的に向上しており、補強性能に優れるものである。ま
た、種類の異なる樹脂を高い比率で混合してもその効果
が維持できることが可能である。このように本発明の樹
脂組成物は、耐衝撃強度及び靱性に優れたものであり、
自動車、家電製品及び電子部品向けなどの機能性複合材
料として有用である。From the results of the examples, since the resin composition of the present invention contains the inorganic filler modified by using the epoxy resin and the silane coupling agent in combination, the silane coupling agent or the epoxy resin is used. Mechanical properties such as tensile strength, tensile elongation, flexural strength, flexural modulus, and Izod impact strength are dramatically improved compared to resin compositions using resin alone, and it has excellent reinforcing performance. It is a thing. Further, even if different kinds of resins are mixed in a high ratio, the effect can be maintained. Thus, the resin composition of the present invention is excellent in impact strength and toughness,
It is useful as a functional composite material for automobiles, home appliances and electronic parts.
Claims (1)
脂、シランカップリング剤及び無機質充填剤を配合する
ことを特徴とする樹脂組成物。1. A resin composition comprising a thermoplastic polyester resin, an epoxy resin, a silane coupling agent and an inorganic filler.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27760493A JPH07102153A (en) | 1993-10-07 | 1993-10-07 | Resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27760493A JPH07102153A (en) | 1993-10-07 | 1993-10-07 | Resin composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH07102153A true JPH07102153A (en) | 1995-04-18 |
Family
ID=17585746
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27760493A Pending JPH07102153A (en) | 1993-10-07 | 1993-10-07 | Resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH07102153A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6974846B2 (en) * | 2002-04-29 | 2005-12-13 | E. I. Du Pont De Nemours And Company | Hydrolysis resistant polyester compositions and related articles and methods |
JP2006249212A (en) * | 2005-03-10 | 2006-09-21 | Riken Technos Corp | Flame retardant resin composition |
JP2006257158A (en) * | 2005-03-15 | 2006-09-28 | Asahi Kasei Chemicals Corp | Reinforced PTT resin composition |
US10815334B2 (en) | 2015-09-04 | 2020-10-27 | Mitsubishi Chemical Corporation | Polyester resin, production method for said polyester resin, and polyester resin composition |
-
1993
- 1993-10-07 JP JP27760493A patent/JPH07102153A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6974846B2 (en) * | 2002-04-29 | 2005-12-13 | E. I. Du Pont De Nemours And Company | Hydrolysis resistant polyester compositions and related articles and methods |
US7008983B2 (en) * | 2002-04-29 | 2006-03-07 | E. I. Du Pont De Nemours And Company | Hydrolysis resistant polyester compositions and related articles and methods |
JP2006249212A (en) * | 2005-03-10 | 2006-09-21 | Riken Technos Corp | Flame retardant resin composition |
JP2006257158A (en) * | 2005-03-15 | 2006-09-28 | Asahi Kasei Chemicals Corp | Reinforced PTT resin composition |
US10815334B2 (en) | 2015-09-04 | 2020-10-27 | Mitsubishi Chemical Corporation | Polyester resin, production method for said polyester resin, and polyester resin composition |
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