JPH10204277A - Thermoplastic resin composition - Google Patents
Thermoplastic resin compositionInfo
- Publication number
- JPH10204277A JPH10204277A JP9008507A JP850797A JPH10204277A JP H10204277 A JPH10204277 A JP H10204277A JP 9008507 A JP9008507 A JP 9008507A JP 850797 A JP850797 A JP 850797A JP H10204277 A JPH10204277 A JP H10204277A
- Authority
- JP
- Japan
- Prior art keywords
- thermoplastic resin
- resin composition
- weight
- polycarbonate resin
- aromatic polycarbonate
- 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.)
- Granted
Links
- 229920005992 thermoplastic resin Polymers 0.000 title claims abstract description 14
- 239000011342 resin composition Substances 0.000 title claims abstract description 12
- 239000004431 polycarbonate resin Substances 0.000 claims abstract description 17
- 229920005668 polycarbonate resin Polymers 0.000 claims abstract description 17
- 125000003118 aryl group Chemical group 0.000 claims abstract description 13
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 11
- 229920001971 elastomer Polymers 0.000 claims abstract description 11
- 239000000806 elastomer Substances 0.000 claims abstract description 11
- 229920000728 polyester Polymers 0.000 claims abstract description 11
- -1 polytetrafluoroethylene Polymers 0.000 claims abstract description 8
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims abstract description 6
- 239000004810 polytetrafluoroethylene Substances 0.000 claims abstract description 6
- 229920002545 silicone oil Polymers 0.000 claims abstract description 4
- 229920000098 polyolefin Polymers 0.000 claims abstract description 3
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 3
- 239000000843 powder Substances 0.000 claims abstract description 3
- 150000001336 alkenes Chemical class 0.000 claims description 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 5
- 239000000203 mixture Substances 0.000 abstract description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 18
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 9
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 8
- 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 8
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000002243 precursor Substances 0.000 description 6
- 239000001993 wax Substances 0.000 description 5
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 4
- 229940058401 polytetrafluoroethylene Drugs 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000004650 carbonic acid diesters Chemical class 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 125000005702 oxyalkylene group Chemical group 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000005809 transesterification reaction Methods 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
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- HCNHNBLSNVSJTJ-UHFFFAOYSA-N 1,1-Bis(4-hydroxyphenyl)ethane Chemical compound C=1C=C(O)C=CC=1C(C)C1=CC=C(O)C=C1 HCNHNBLSNVSJTJ-UHFFFAOYSA-N 0.000 description 1
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 1
- YMTYZTXUZLQUSF-UHFFFAOYSA-N 3,3'-Dimethylbisphenol A Chemical compound C1=C(O)C(C)=CC(C(C)(C)C=2C=C(C)C(O)=CC=2)=C1 YMTYZTXUZLQUSF-UHFFFAOYSA-N 0.000 description 1
- VWGKEVWFBOUAND-UHFFFAOYSA-N 4,4'-thiodiphenol Chemical compound C1=CC(O)=CC=C1SC1=CC=C(O)C=C1 VWGKEVWFBOUAND-UHFFFAOYSA-N 0.000 description 1
- NZGQHKSLKRFZFL-UHFFFAOYSA-N 4-(4-hydroxyphenoxy)phenol Chemical compound C1=CC(O)=CC=C1OC1=CC=C(O)C=C1 NZGQHKSLKRFZFL-UHFFFAOYSA-N 0.000 description 1
- ODJUOZPKKHIEOZ-UHFFFAOYSA-N 4-[2-(4-hydroxy-3,5-dimethylphenyl)propan-2-yl]-2,6-dimethylphenol Chemical compound CC1=C(O)C(C)=CC(C(C)(C)C=2C=C(C)C(O)=C(C)C=2)=C1 ODJUOZPKKHIEOZ-UHFFFAOYSA-N 0.000 description 1
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- SDDLEVPIDBLVHC-UHFFFAOYSA-N Bisphenol Z Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)CCCCC1 SDDLEVPIDBLVHC-UHFFFAOYSA-N 0.000 description 1
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000004419 Panlite Substances 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- QLVWOKQMDLQXNN-UHFFFAOYSA-N dibutyl carbonate Chemical compound CCCCOC(=O)OCCCC QLVWOKQMDLQXNN-UHFFFAOYSA-N 0.000 description 1
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000001175 rotational moulding Methods 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、機械的強度、耐熱
性等が良好な熱可塑性樹脂組成物に関し、さらには傷付
き防止性に優れた熱可塑性樹脂組成物に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a thermoplastic resin composition having good mechanical strength and heat resistance, and more particularly to a thermoplastic resin composition having excellent scratch resistance.
【0002】[0002]
【従来の技術】芳香族ポリカーボネート樹脂は、機械的
強度、耐熱性等に優れたエンジニアリングプラスチック
であり、電気、電子機器分野等さまざまな分野において
幅広く利用されている。特に容器等の成形品にはその優
れた特性により多く使用されている。しかしながら、容
器に入れる成形品、特にその成形品がポリカーボネート
樹脂よりなる成形品ではその成形品を傷つける問題があ
る。これを改良する方法の一つとして特公昭36−76
41、特開昭48−40849等に記載されているよう
にシリコーンオイルや、ポリテトラフルオロエチレンと
オレフィン系ワックス等を添加して摺動特性を向上させ
ることは傷付き防止に有効であるが、まだ不十分であっ
た。2. Description of the Related Art Aromatic polycarbonate resins are engineering plastics having excellent mechanical strength and heat resistance, and are widely used in various fields such as electric and electronic equipment. Particularly, molded articles such as containers are often used because of their excellent properties. However, there is a problem that the molded article put in a container, particularly the molded article made of a polycarbonate resin, may damage the molded article. One of the methods for improving this is Japanese Patent Publication No. 36-76.
41, as described in JP-A-48-40849, etc., it is effective to improve the sliding properties by adding silicone oil, polytetrafluoroethylene and an olefin wax, etc. Still not enough.
【0003】[0003]
【発明が解決しようとする課題】本発明の目的は、機械
的強度、耐熱性等が良好でさらに傷付き防止性に優れた
熱可塑性樹脂組成物を提供することにある。SUMMARY OF THE INVENTION An object of the present invention is to provide a thermoplastic resin composition having good mechanical strength, heat resistance and the like and further having excellent scratch resistance.
【0004】本発明者は、上記目的を達成すべく鋭意研
究を重ねた結果、芳香族ポリカーボネート樹脂にポリエ
ステルエラストマーを配合することにより成形品表面の
硬度を低下させ、さらに摺動性付与剤を配合することに
より摩擦抵抗を低減させることで目的とする傷付き防止
に優れ、尚かつ機械的強度、耐熱性等が良好な熱可塑性
樹脂組成物が得られることを見いだし、本発明に到達し
た。The inventor of the present invention has conducted intensive studies to achieve the above object. As a result, the hardness of the molded article surface is reduced by blending a polyester elastomer with an aromatic polycarbonate resin, and further, a slidability imparting agent is blended. The present inventors have found that by reducing the frictional resistance, it is possible to obtain a thermoplastic resin composition which is excellent in prevention of intended scratching and has good mechanical strength, heat resistance and the like, and has reached the present invention.
【0005】[0005]
【課題を解決するための手段】すなわち、本発明によれ
ば(A)芳香族ポリカーボネート樹脂94.9〜65重
量%、(B)ポリエステルエラストマー5〜30重量
%、(C)摺動性付与剤0.1〜5重量%よりなる熱可
塑性樹脂組成物が提供される。According to the present invention, (A) 94.9 to 65% by weight of an aromatic polycarbonate resin, (B) 5 to 30% by weight of a polyester elastomer, and (C) a slidability imparting agent. A thermoplastic resin composition comprising 0.1 to 5% by weight is provided.
【0006】本発明において(A)成分として使用され
る芳香族ポリカーボネート樹脂は通常エンジニアリング
樹脂として使用される樹脂であり、二価フェノールとカ
ーボネート前駆体を反応させて得られる芳香族ポリカー
ボネート樹脂である。ここで使用する二価フェノールの
代表的な例としては、2,2−ビス(4−ヒドロキシフ
ェニル)プロパン(通称ビスフェノールA)、ビス(4
−ヒドロキシフェニル)メタン、1,1−ビス(4−ヒ
ドロキシフェニル)エタン、1,1−ビス(4−ヒドロ
キシフェニル)シクロヘキサン、2,2−ビス(4−ヒ
ドロキシ−3,5−ジメチルフェニル)プロパン、2,
2−ビス(4ヒドロキシ−3,5ジブロモフェニル)プ
ロパン、2,2−ビス(4−ヒドロキシ−3−メチルフ
ェニル)プロパン、ビス(4−ヒドロキシフェニル)エ
ーテル、4−4’−ジヒドロキシジフェニル、ビス(4
−ヒドロキシフェニル)サルファイドおよびビス(4−
ヒドロキシフェニル)スルホン等があげられる。好まし
い二価フェノールはビス(4−ヒドロキシフェニル)ア
ルカンであり、なかでもビスフェノールAが特に好まし
い。The aromatic polycarbonate resin used as the component (A) in the present invention is a resin usually used as an engineering resin, and is an aromatic polycarbonate resin obtained by reacting a dihydric phenol with a carbonate precursor. Representative examples of the dihydric phenol used here include 2,2-bis (4-hydroxyphenyl) propane (commonly called bisphenol A) and bis (4
-Hydroxyphenyl) methane, 1,1-bis (4-hydroxyphenyl) ethane, 1,1-bis (4-hydroxyphenyl) cyclohexane, 2,2-bis (4-hydroxy-3,5-dimethylphenyl) propane , 2,
2-bis (4hydroxy-3,5dibromophenyl) propane, 2,2-bis (4-hydroxy-3-methylphenyl) propane, bis (4-hydroxyphenyl) ether, 4-4′-dihydroxydiphenyl, bis (4
-Hydroxyphenyl) sulfide and bis (4-
(Hydroxyphenyl) sulfone and the like. Preferred dihydric phenols are bis (4-hydroxyphenyl) alkanes, of which bisphenol A is particularly preferred.
【0007】本発明における(A)成分の芳香族ポリカ
ーボネート樹脂の製造方法について基本的な手段を簡単
に説明する。The basic means for producing the aromatic polycarbonate resin as the component (A) in the present invention will be briefly described.
【0008】カーボネート前駆物質として例えばホスゲ
ンを使用する溶液法の場合、通常酸結合剤および溶媒の
存在下に反応を行う。酸結合剤としては例えば水酸化ナ
トリウム、水酸化カリウム等のアルカリ金属水酸化物ま
たはピリジン等のアミン化合物が用いられる。溶媒とし
ては例えば塩化メチレン、クロロベンゼン等のハロゲン
化炭化水素が用いられる。また反応促進のために例えば
第三級アミンまたは第四級アンモニウム塩等の触媒を用
いることもできる。その際、反応温度は通常0〜40℃
であり、反応時間は数分〜5時間である。この溶液法の
ホスゲン以外のカーボネート前駆体としては、カーボネ
ートエステルまたはハロホルメート等が使用でき、具体
的にはジフェニルカーボネートまたは二価フェノールの
ジハロホルメート等が挙げられる。In the case of the solution method using, for example, phosgene as the carbonate precursor, the reaction is usually carried out in the presence of an acid binder and a solvent. Examples of the acid binder include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide and amine compounds such as pyridine. As the solvent, for example, halogenated hydrocarbons such as methylene chloride and chlorobenzene are used. For promoting the reaction, a catalyst such as a tertiary amine or a quaternary ammonium salt may be used. At that time, the reaction temperature is usually 0 to 40 ° C.
And the reaction time is a few minutes to 5 hours. As a carbonate precursor other than phosgene in this solution method, a carbonate ester or a haloformate can be used, and specific examples include diphenyl carbonate or a dihaloformate of a dihydric phenol.
【0009】カーボネート前駆物質として炭酸ジエステ
ルを用いるエステル交換反応(溶融法)は、不活性ガス
雰囲気下所定割合の二価フェノール成分を炭酸ジエステ
ルと加熱しながら撹拌して、生成するアルコールまたは
フェノール類を留出させる方法により行われる。反応温
度は生成するアルコールまたはフェノール類の沸点等に
より異なるが、通常120〜300℃の範囲である。反
応はその初期から減圧にして生成するアルコールまたは
フェノール類を留出させながら反応を完結させる。また
反応を促進するために通常エステル交換反応に使用され
る触媒を使用することもできる。前記エステル交換反応
に使用される炭酸ジエステルとしては、例えばジフェニ
ルカーボネート、ジナフチルカーボネート、ビス(ジフ
ェニル)カーボネート、ジメチルカーボネート、ジエチ
ルカーボネート、ジブチルカーボネート等が挙げられ
る。これらのうち特にジフェニルカーボネートが好まし
い。In a transesterification reaction (melting method) using a carbonic acid diester as a carbonate precursor, a predetermined ratio of a dihydric phenol component is stirred with a carbonic acid diester under heating in an inert gas atmosphere to produce alcohol or phenols. It is carried out by a method of distilling. The reaction temperature varies depending on the boiling point of the produced alcohol or phenol, and is usually in the range of 120 to 300 ° C. The reaction is completed under reduced pressure from the beginning while distilling off alcohol or phenols produced. Further, a catalyst usually used in a transesterification reaction to promote the reaction can be used. Examples of the carbonic acid diester used in the transesterification reaction include diphenyl carbonate, dinaphthyl carbonate, bis (diphenyl) carbonate, dimethyl carbonate, diethyl carbonate, dibutyl carbonate and the like. Of these, diphenyl carbonate is particularly preferred.
【0010】上記二価フェノールとカーボネート前駆体
を反応させて芳香族ポリカーボネート樹脂を製造するに
当たり、二価フェノールは単独または2種以上を使用す
ることができ、また芳香族ポリカーボネート樹脂は三官
能以上の他官能性芳香族化合物を共重合した分岐ポリカ
ーボネート樹脂であっても、2種以上の芳香族ポリカー
ボネート樹脂の混合物であってもよい。また、必要に応
じて触媒、分子量調節剤、酸化防止剤を使用してもよ
い。In producing the aromatic polycarbonate resin by reacting the above-mentioned dihydric phenol with a carbonate precursor, the dihydric phenol may be used alone or in combination of two or more. It may be a branched polycarbonate resin obtained by copolymerizing a polyfunctional aromatic compound or a mixture of two or more aromatic polycarbonate resins. Further, if necessary, a catalyst, a molecular weight regulator and an antioxidant may be used.
【0011】芳香族ポリカーボネート樹脂の分子量につ
いては任意のものを用いることができ、例えば二価フェ
ノールとしてビスフェノールA、カーボネート前駆体と
してホスゲンを用いて芳香族ポリカーボネート樹脂を得
た場合、濃度0.7g/dl塩化メチレン溶液により温
度20℃で測定した比粘度(ηsp)が0.15〜1.
5のものが好ましい。Any molecular weight can be used for the aromatic polycarbonate resin. For example, when an aromatic polycarbonate resin is obtained using bisphenol A as a dihydric phenol and phosgene as a carbonate precursor, a concentration of 0.7 g / The specific viscosity (ηsp) measured at a temperature of 20 ° C. with a dl methylene chloride solution is 0.15 to 1.
Five are preferred.
【0012】本発明で(B)成分として使用されるポリ
エステルエラストマーは、テレフタル酸を70モル%以
上含有するジカルボン酸、テトラメチレングリコールを
70モル%以上含有するグリコール成分、および平均分
子量が500〜5000のポリ(オキシアルキレン)グ
リコールの三成分を共重合させた共重合体である。The polyester elastomer used as the component (B) in the present invention comprises a dicarboxylic acid containing at least 70 mol% of terephthalic acid, a glycol component containing at least 70 mol% of tetramethylene glycol, and an average molecular weight of 500 to 5,000. Is a copolymer obtained by copolymerizing three components of poly (oxyalkylene) glycol.
【0013】ポリ(オキシアルキレン)グリコールとし
ては、平均分子量が500〜5000でありこのグリコ
ール中に含有される炭素原子と酸素原子との数の比が
2.0〜4.3であることが好ましく、例えばポリ(テ
トラメチレンオキサイド)グリコール、ポリ(エチレン
オキサイド)グリコール、ポリ(プロピレンオキサイ
ド)グリコールおよびこれらの共重合体等があげられ、
特にポリ(テトラメチレンオキサイド)グリコールが好
ましい。ポリエステルエラストマー中のポリ(オキシア
ルキレン)グリコール量は20〜80重量%であり、好
ましくは30〜80重量%であり、特に好ましくは50
〜80重量%である。ポリエステルエラストマーの重合
度は、35℃オルソクロロフェノール中1.2g/10
0mlの濃度で測定した還元粘度が0.5〜5.0のも
のが好ましく、特に0.7〜4.0のものが好ましい。The poly (oxyalkylene) glycol preferably has an average molecular weight of 500 to 5,000 and a ratio of the number of carbon atoms to oxygen atoms contained in the glycol of 2.0 to 4.3. Examples thereof include poly (tetramethylene oxide) glycol, poly (ethylene oxide) glycol, poly (propylene oxide) glycol, and copolymers thereof.
Particularly, poly (tetramethylene oxide) glycol is preferable. The amount of poly (oxyalkylene) glycol in the polyester elastomer is from 20 to 80% by weight, preferably from 30 to 80% by weight, particularly preferably from 50 to 80% by weight.
~ 80% by weight. The degree of polymerization of the polyester elastomer is 1.2 g / 10
Those having a reduced viscosity of 0.5 to 5.0 measured at a concentration of 0 ml are preferred, and those having a reduced viscosity of 0.7 to 4.0 are particularly preferred.
【0014】このポリエステルエラストマーの配合量
は、5〜30重量%であり、10〜20重量%の範囲が
好ましい。5重量%未満では表面硬度の低下が少ないた
め、傷付き防止性が劣り、30重量%を越えると耐熱性
が低下するため好ましくない。The amount of the polyester elastomer is 5 to 30% by weight, preferably 10 to 20% by weight. If it is less than 5% by weight, the decrease in surface hardness is small, so that the anti-scratch property is inferior.
【0015】本発明で(C)成分として使用される摺動
性付与剤とは該樹脂成分に摺動性を付与する添加剤であ
る。この添加剤は摺動性を付与するものであれば特に限
定されるものではない。摺動性を付与する添加剤として
はポリオレフィン、オレフィン系ワックス、ポリテトラ
フルオロエチレン、シリコーンパウダー、シリコーンオ
イル等があげられる。これらのなかでは摺動特性と機械
的強度のバランスが優れるオレフィン系ワックス、ポリ
テトラフルオロエチレンの単独又は併用が好ましい。The slidability imparting agent used as the component (C) in the present invention is an additive which imparts slidability to the resin component. This additive is not particularly limited as long as it imparts slidability. Examples of additives that impart slidability include polyolefin, olefin-based wax, polytetrafluoroethylene, silicone powder, and silicone oil. Of these, olefin waxes and polytetrafluoroethylene, which have an excellent balance between sliding characteristics and mechanical strength, are preferably used alone or in combination.
【0016】この摺動性付与剤の配合量は、0.1〜5
重量%であり、0.5〜3重量%の範囲が好ましい。
0.1重量%未満では充分な摺動特性が得られないた
め、傷付き防止性が劣り、5重量%を越えると剥離、機
械的強度の低下等が生じるため好ましくない。The compounding amount of the slidability imparting agent is 0.1 to 5
%, Preferably in the range of 0.5 to 3% by weight.
If the amount is less than 0.1% by weight, sufficient sliding properties cannot be obtained, so that the anti-scratch property is poor. If the amount exceeds 5% by weight, peeling, reduction in mechanical strength, and the like occur, which is not preferable.
【0017】本発明の熱可塑性樹脂組成物の上記各成分
の割合は、(A)成分、(B)成分及び(C)成分の合
計が100重量%になるよう調整し、さらに、本発明の
目的および効果を損なわない範囲で、難燃剤、難燃助
剤、着色剤、帯電防止剤等を配合してもよく、また他の
熱可塑性樹脂を配合しても良い。The proportion of each of the above components of the thermoplastic resin composition of the present invention is adjusted so that the total of the components (A), (B) and (C) becomes 100% by weight. A flame retardant, a flame retardant auxiliary, a coloring agent, an antistatic agent and the like may be blended as long as the purpose and the effect are not impaired, and other thermoplastic resins may be blended.
【0018】また、本発明によれば、該熱可塑性樹脂組
成物を溶融混練し、成形して得られた成形品が提供され
る。この成形品は、各成分を混合機、例えばV型ブレン
ダー、リボンミキサーまたはタンブラー等に投入し均一
に混合した後、一軸または二軸押出機で溶融混練し、さ
らに射出成形、圧縮成形または回転成形等の方法で成形
することにより得られる。また、成分の一部を予め混合
混練後、さらに残りの成分を添加し混練、溶融押出して
もよい。Further, according to the present invention, there is provided a molded product obtained by melt-kneading and molding the thermoplastic resin composition. This molded product is charged into a mixer, for example, a V-blender, a ribbon mixer or a tumbler, and uniformly mixed, and then melt-kneaded with a single-screw or twin-screw extruder, followed by injection molding, compression molding or rotational molding. And the like. Alternatively, after some of the components are previously mixed and kneaded, the remaining components may be further added, kneaded, and melt-extruded.
【0019】[0019]
【実施例】以下、実施例を挙げて本発明を更に詳しく説
明する。なお、評価は下記(1)〜(4)の方法によっ
た。EXAMPLES Hereinafter, the present invention will be described in more detail by way of examples. The evaluation was performed according to the following methods (1) to (4).
【0020】(1)耐衝撃性:ASTM D256に従
い、厚さ1/4″試験片にてノッチ付きアイゾット衝撃
強度を測定した。(1) Impact resistance: Notched Izod impact strength of a 1/4 ″ test piece was measured according to ASTM D256.
【0021】(2)耐熱性:ASTM D648に従
い、18.6kgf/cm2 荷重の荷重たわみ温度を測定し
た。(2) Heat resistance: The deflection temperature under a load of 18.6 kgf / cm 2 was measured in accordance with ASTM D648.
【0022】(3)表面硬度:JISK5400に準拠
し、おもり1kg、鉛筆の移動速度0.5mm/secでの鉛筆
硬度をを測定した。尚、判定は試験片の表面に傷が付か
ないときの鉛筆の硬度を表面硬度とした。(3) Surface hardness: Pencil hardness at a weight of 1 kg and a pencil moving speed of 0.5 mm / sec was measured in accordance with JIS K5400. In addition, the hardness of the pencil when the surface of the test piece was not damaged was determined as the surface hardness.
【0023】(4)動摩擦係数:外径25mm、内径2
0mmの円筒状試験片を作成し、摩擦試験機((株)オ
リエンテック製 フリクトロン摩擦摩耗試験機)をスラ
スト摩擦摩耗試験を行った。滑り速度20cm/sec 、相
手材料は機械構造用炭素鋼(S−45C)を使用し、無
潤滑の状態での動摩擦係数を測定した。(4) Coefficient of dynamic friction: outer diameter 25 mm, inner diameter 2
A 0 mm cylindrical test piece was prepared, and a friction tester (Frictron friction and wear tester manufactured by Orientec Co., Ltd.) was subjected to a thrust friction and wear test. The sliding speed was 20 cm / sec, and the partner material was carbon steel for machine structural use (S-45C), and the dynamic friction coefficient in an unlubricated state was measured.
【0024】[実施例1〜5、および比較例1〜7]ポ
リカーボネート樹脂、ポリエステルエラストマー、摺動
性付与剤、および安定剤を表1に示す割合でV型ブレン
ダーで混合し、径30mmのベント式二軸押出機
((株)日本製鋼所製TEX30XSSTによりシリン
ダー温度270℃でペレット化し、このペレットを11
0℃で5時間乾燥した後、射出成形機(ファナック
(株)製 T−150D)によりシリンダー温度270
℃、金型温度70℃で試験片を作成し、これらの評価結
果を表1に示した。なお、表1記載の各成分を示す記号
は下記の通りである。[Examples 1 to 5 and Comparative Examples 1 to 7] A polycarbonate resin, a polyester elastomer, a slidability-imparting agent and a stabilizer were mixed in the proportions shown in Table 1 in a V-type blender to form a vent having a diameter of 30 mm. A twin-screw extruder (TEX30XSST manufactured by Japan Steel Works, Ltd.) pelletized at a cylinder temperature of 270 ° C.
After drying at 0 ° C. for 5 hours, the cylinder temperature was 270 using an injection molding machine (T-150D, manufactured by FANUC CORPORATION).
Test pieces were prepared at a temperature of 70 ° C. and a mold temperature of 70 ° C. The evaluation results are shown in Table 1. In addition, the symbol which shows each component of Table 1 is as follows.
【0025】PC:ポリカーボネート樹脂[帝人化成
(株)製パンライトL−1225、ηsp=0.41] PTEE:ポリエステルエラストマー[帝人(株)製ヌ
ーベランTR−ER1] 摺動性付与剤1:ポリテトラフルオロエチレン樹脂[ダ
イキン工業(株)製ルブロンL−5] 摺動性付与剤2:オレフィン系ワックス[三井石油化学
(株)製ハイワックス310MP]PC: Polycarbonate resin [Panlite L-1225, ηsp = 0.41, manufactured by Teijin Chemicals Ltd.] PTEE: Polyester elastomer [Nuvellan TR-ER1, manufactured by Teijin Limited] Sliding agent 1: Polytetra Fluoroethylene resin [Lubron L-5 manufactured by Daikin Industries, Ltd.] Sliding property imparting agent 2: olefin-based wax [High wax 310MP manufactured by Mitsui Petrochemical Co., Ltd.]
【0026】[0026]
【表1】 [Table 1]
【0027】[0027]
【発明の効果】本発明の熱可塑性樹脂は、傷付き防止
性、機械的強度、耐熱性に優れるため、容器等の成形品
に有用である。The thermoplastic resin of the present invention is useful for molded articles such as containers because it has excellent scratch resistance, mechanical strength and heat resistance.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI (C08L 69/00 67:00 83:04) (C08L 67/00 69:00 23:00) ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code FI (C08L 69/00 67:00 83:04) (C08L 67/00 69:00 23:00)
Claims (2)
4.9〜65重量%、(B)ポリエステルエラストマー
5〜30重量%、(C)摺動性付与剤0.1〜5重量%
よりなる熱可塑性樹脂組成物。(A) Aromatic polycarbonate resin 9
4.9-65% by weight, (B) 5-30% by weight of a polyester elastomer, (C) 0.1-5% by weight of a slidability imparting agent
A thermoplastic resin composition comprising:
オレフィン系ワックス、ポリテトラフルオロエチレン、
シリコーンパウダー、シリコーンオイルより選ばれた1
種または2種以上である請求項1記載の熱可塑性樹脂組
成物。(C) The slidability imparting agent is a polyolefin,
Olefin wax, polytetrafluoroethylene,
1 selected from silicone powder and silicone oil
The thermoplastic resin composition according to claim 1, wherein the thermoplastic resin composition is a kind or two or more kinds.
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JP00850797A JP3876032B2 (en) | 1997-01-21 | 1997-01-21 | Thermoplastic resin composition |
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JPH10204277A true JPH10204277A (en) | 1998-08-04 |
JP3876032B2 JP3876032B2 (en) | 2007-01-31 |
Family
ID=11695047
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010070715A (en) * | 2008-09-22 | 2010-04-02 | Teijin Chem Ltd | Flame-retardant aromatic polycarbonate resin composition |
CN109401161A (en) * | 2018-12-11 | 2019-03-01 | 广东天雄新材料科技股份有限公司 | Exempt from spraying, high durable, the PMMA material of scratch-resistant and preparation method thereof |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60260647A (en) * | 1984-05-19 | 1985-12-23 | バイエル・アクチエンゲゼルシヤフト | Thermoplastic forming composition and manufacture |
JPH01234461A (en) * | 1987-12-16 | 1989-09-19 | General Electric Co <Ge> | Polycarbonate composition having low heating stress temperature |
JPH0665492A (en) * | 1992-08-17 | 1994-03-08 | Teijin Chem Ltd | Resin composition for block handle of toothbrush |
JPH06248190A (en) * | 1993-02-22 | 1994-09-06 | Denki Kagaku Kogyo Kk | Slippery thermoplastic resin composition |
JPH08501328A (en) * | 1992-07-08 | 1996-02-13 | カワサキ ケミカル ホールディング シーオー. | Elastomer toughening wear resistant composition |
JPH08283494A (en) * | 1995-04-12 | 1996-10-29 | Otsuka Chem Co Ltd | Resin composition for sliding member |
JPH093313A (en) * | 1995-06-22 | 1997-01-07 | Teijin Chem Ltd | Sliding resin composition and molded article formed therefrom |
JPH09194743A (en) * | 1996-01-16 | 1997-07-29 | Otsuka Chem Co Ltd | Vibration-damping thermoplastic resin composition |
JPH09302209A (en) * | 1996-05-14 | 1997-11-25 | Teijin Chem Ltd | Resin composition and molded article obtained therefrom |
-
1997
- 1997-01-21 JP JP00850797A patent/JP3876032B2/en not_active Expired - Fee Related
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60260647A (en) * | 1984-05-19 | 1985-12-23 | バイエル・アクチエンゲゼルシヤフト | Thermoplastic forming composition and manufacture |
JPH01234461A (en) * | 1987-12-16 | 1989-09-19 | General Electric Co <Ge> | Polycarbonate composition having low heating stress temperature |
JPH08501328A (en) * | 1992-07-08 | 1996-02-13 | カワサキ ケミカル ホールディング シーオー. | Elastomer toughening wear resistant composition |
JPH0665492A (en) * | 1992-08-17 | 1994-03-08 | Teijin Chem Ltd | Resin composition for block handle of toothbrush |
JPH06248190A (en) * | 1993-02-22 | 1994-09-06 | Denki Kagaku Kogyo Kk | Slippery thermoplastic resin composition |
JPH08283494A (en) * | 1995-04-12 | 1996-10-29 | Otsuka Chem Co Ltd | Resin composition for sliding member |
JPH093313A (en) * | 1995-06-22 | 1997-01-07 | Teijin Chem Ltd | Sliding resin composition and molded article formed therefrom |
JPH09194743A (en) * | 1996-01-16 | 1997-07-29 | Otsuka Chem Co Ltd | Vibration-damping thermoplastic resin composition |
JPH09302209A (en) * | 1996-05-14 | 1997-11-25 | Teijin Chem Ltd | Resin composition and molded article obtained therefrom |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010070715A (en) * | 2008-09-22 | 2010-04-02 | Teijin Chem Ltd | Flame-retardant aromatic polycarbonate resin composition |
CN109401161A (en) * | 2018-12-11 | 2019-03-01 | 广东天雄新材料科技股份有限公司 | Exempt from spraying, high durable, the PMMA material of scratch-resistant and preparation method thereof |
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