JPS61130367A - Outer shell of electric equipment - Google Patents
Outer shell of electric equipmentInfo
- Publication number
- JPS61130367A JPS61130367A JP25055484A JP25055484A JPS61130367A JP S61130367 A JPS61130367 A JP S61130367A JP 25055484 A JP25055484 A JP 25055484A JP 25055484 A JP25055484 A JP 25055484A JP S61130367 A JPS61130367 A JP S61130367A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- outer shell
- glass fiber
- polycarbonate
- acrylic
- 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
- 239000003365 glass fiber Substances 0.000 claims abstract description 21
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229920000642 polymer Polymers 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 9
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 239000004417 polycarbonate Substances 0.000 abstract description 11
- 229920000515 polycarbonate Polymers 0.000 abstract description 10
- 238000000465 moulding Methods 0.000 abstract description 6
- 239000003963 antioxidant agent Substances 0.000 abstract description 2
- 230000003078 antioxidant effect Effects 0.000 abstract description 2
- 239000000945 filler Substances 0.000 abstract description 2
- 239000003381 stabilizer Substances 0.000 abstract description 2
- 229920000800 acrylic rubber Polymers 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 239000003086 colorant Substances 0.000 abstract 1
- 229920000058 polyacrylate Polymers 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 238000002156 mixing Methods 0.000 description 6
- -1 iron Chemical class 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000008188 pellet Substances 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 150000002989 phenols Chemical class 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 239000004431 polycarbonate resin Substances 0.000 description 2
- 229920005668 polycarbonate resin Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920005990 polystyrene resin Polymers 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 239000004419 Panlite Substances 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000006085 branching agent Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- HDQDUBPEBVXIBJ-UHFFFAOYSA-N hept-1-en-1-ol Chemical compound CCCCCC=CO HDQDUBPEBVXIBJ-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Organic Insulating Materials (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は電気機器の外殻に関し、詳しくは電気特性、特
に耐トラツキング性に優れるとともに成械的強度、耐熱
性に優れたガラス繊維強化樹脂より成るクラスI電気機
器の外殻に関するものである。[Detailed Description of the Invention] <Industrial Application Field> The present invention relates to the outer shell of electrical equipment, and more specifically to a glass fiber reinforced resin that has excellent electrical properties, particularly tracking resistance, as well as excellent mechanical strength and heat resistance. The outer shell of a class I electrical device consists of:
〈従来技術〉
電気機器の外かくは使用用途、環境にもよるが一般的に
、機械的強度、耐熱性、寸法安定性、電気特性、特に耐
トラツキング性に優れ【いろことが要求される。例えば
機械的強度では電気機器を使用時、誤って下に落下させ
たり、他の堅い物質、例えば鉄等の金属を電気機器の上
に落下させても割れたり変形したりしな〜機械的強度が
必要である。鬼気特性では汚染による轡緻破壊を予防す
るために電気機器の外かくの耐トラツキング性が優れて
いることが必要である。特に電気ドリル、電気かんな、
電気のこ、電気グラインダー等のクラス菖電気機器の外
かくでは曲げ弾性率40、 OO0kllf/−以上、
耐トラツキング性(xg。<Prior Art> The exterior of electrical equipment is generally required to have excellent mechanical strength, heat resistance, dimensional stability, and electrical properties, especially tracking resistance, although it depends on the intended use and environment. For example, in terms of mechanical strength, when an electrical device is in use, it will not crack or deform even if it is accidentally dropped or other hard materials, such as metals such as iron, are dropped on top of the device. is necessary. In order to prevent detailed damage due to contamination, it is necessary for the exterior of electrical equipment to have excellent tracking resistance. Especially electric drills, electric planers,
For the exterior of class electric equipment such as electric saws and electric grinders, the bending elastic modulus is 40, OO0kllf/- or more,
Tracking resistance (xg.
Publication 112 ) P T I 1
75 V以上が必要である。
、従来よりこれらの電気機器の外か(は、ガラ
ス繊維強化人BB樹脂、ガラス繊維強化ポリプロピレン
樹脂、ガラス繊維強化ポリスチレン樹脂、ガラス繊維強
化ポリアミド樹脂、ガラス繊維強化ポリカーボネート樹
脂等で作られている。Publication 112) PTI 1
75 V or more is required.
Traditionally, these electrical appliances have been made of glass fiber reinforced BB resin, glass fiber reinforced polypropylene resin, glass fiber reinforced polystyrene resin, glass fiber reinforced polyamide resin, glass fiber reinforced polycarbonate resin, etc.
しかしながら、上記のガラス繊維強化ポリプロビレ/樹
脂、或は、ガラス繊維強化ポリスチレン樹脂製のものは
、機械的強度、耐熱性に劣るため使用可能な分野が制限
される。However, the above-mentioned glass fiber-reinforced polypropylene/resin or glass fiber-reinforced polystyrene resin has poor mechanical strength and heat resistance, so that the fields in which it can be used are limited.
ガラス繊維強化ポリアミド樹脂製のものは機械的強度、
耐熱性は良いが、Wk温くより寸法が変化しやすく、外
かくとしての寸法安定性に劣る。また、ガラス繊維強化
ポリカーボネート樹脂製のものは、機械的強度、耐熱性
寸法安尼性は良いが、耐トラツキング性が不安定である
。Those made of glass fiber reinforced polyamide resin have mechanical strength,
Although it has good heat resistance, its dimensions change more easily than when WK is warmer, and its dimensional stability as an external shell is poor. Further, those made of glass fiber reinforced polycarbonate resin have good mechanical strength, heat resistance and dimensional stability, but have unstable tracking resistance.
〈発明の目的〉
本発明の目的は、耐トラツキング性く優れるとともく、
機械的強度、耐熱性に優れたりφ
ラス厘電気機器外殻を提供するごとくある。<Objective of the Invention> The object of the present invention is to provide excellent tracking resistance and to
It has excellent mechanical strength and heat resistance, and is used to provide outer shells for electrical equipment.
〈発明の構成〉
本発明は(A)芳香族ポリカーボネー) 99.5〜8
0重量% (B)アクリル系弾性重合体0.5〜20重
1%から成る組成物100重量部に対してガラス繊維を
5〜70重量部配合して成形された事を特徴とするクラ
ス■電気機器の外かくである。<Structure of the Invention> The present invention relates to (A) aromatic polycarbonate) 99.5 to 8
0% by weight (B) Class ■ characterized by being molded by blending 5 to 70 parts by weight of glass fiber to 100 parts by weight of a composition consisting of 0.5 to 20% by weight of an acrylic elastic polymer. This is the exterior of electrical equipment.
本発明において使用する芳香族ポリカーボネート(A)
は、2価フェノールより誘導される平均分子JIL 1
0,000〜100,000、好ましくは15,00
Q〜6 Q、000のポリカーボネートであり、通常2
価フェノールとカーボネート前駆体との溶液法あるいは
溶融法で製造される62価フェノールの代表的な例を挙
げるとビス7二/−ル人〔2F2−ビス(4−ヒトツキ
ジフェノール)ブーパン)〕、ビス(4−ヒト−キシ7
エ二ル)メタン、1.1−ヒス(4−ヒトジキシフェニ
ル)エタン、2,2−ビス(4−ヒドロキシ−3−メチ
ルフェニル)プシバン等がある。好ましい2価フェノー
ルはビス(4−tドロキシフェニル)アルカン系化合吻
、特にビスフェノール人である。2価フェノールは単独
で、あるいは2種以上風合して使用することができる。Aromatic polycarbonate (A) used in the present invention
is the average molecule JIL 1 derived from dihydric phenol
0,000-100,000, preferably 15,00
Q~6 Q,000 polycarbonate, usually 2
Typical examples of 62-valent phenols produced by a solution method or a melting method using a phenol and a carbonate precursor include bis72/-[2F2-bis(4-human diphenol) boupan]; bis(4-human-xy7
enyl)methane, 1,1-his(4-hydoxyphenyl)ethane, 2,2-bis(4-hydroxy-3-methylphenyl)pusiban, and the like. Preferred dihydric phenols are bis(4-t-droxyphenyl)alkanes, especially bisphenols. Dihydric phenols can be used alone or in combination of two or more types.
また前記カーボネート前駆体としては、カルボニルパラ
イト、カーボネートあるいはハロホルメ゛−ト等を挙げ
ることができる。Examples of the carbonate precursor include carbonylpallite, carbonate, and haloformate.
代表的な例としては、ホスゲン、ジフェニルカーボネー
ト、2価7エノールのジノ10ホルメート及びこれらの
混合物があげられろ。Representative examples include phosgene, diphenyl carbonate, dino-10 formate of divalent heptaenol, and mixtures thereof.
芳香族ポリカーボネートの製造に際しては適当な分子m
調整剤、分岐剤、触媒等も使用できる。When producing aromatic polycarbonate, a suitable molecule m
Conditioners, branching agents, catalysts, etc. can also be used.
本発明において用いられるアクリル系弾性重合体(B)
は、アクリル酸エステルを主成分とするメタクリル酸エ
ステル、ブタジェン、スチレン、アクリロニトリル喀の
如き共重合モノマーとの共重合体であって、例えばアル
キル基の炭素数が2〜12アクリルばアルキル(例えば
2−エチルへキシルアクリレート、n−ブチルアクリレ
ート等)40〜95重量%とブタジェン5〜40mff
1%とメチルメタクリレート0〜30重量%及び0.0
1〜3重量%の架橋剤(例えばエチレンジメタクリレー
ト等)からなる混合単量体を乳化重合し、これに凝巣剤
を添加しC得られろ平均校径OJ〜0.3μの架橋ゴム
共重合体50〜80重量部を含むラテックスに、まずス
チレン20〜80重量%とメチルメタクリレート20〜
50!1ffi%とアクリ−ニトリルO〜60Jij1
%およびim剤(例えばエチレンジメタクリレート、ジ
ビニルベンゼン等)、0.1〜2m[m%の毘合単量体
10〜40重量部を添加重合した後、架橋剤(例えばエ
チレンジメタクリレート、ジビニルベンゼン等)0.1
〜4重量%を含むアルキル基の炭素数が1〜4のメタク
リル酸アルキル(例えばメチルメタクリレート等)5〜
25重量部を更に添加1合して得られる多成分系樹脂で
ある。かρ)るアクリル系弾性重合体の具体例としては
呉羽化学工業■から製品名HI人−15として市販され
ているものが例示される。アクリル系弾性重合体(B)
を添加することによりポリカーボネート・つ附トラッキ
ング性が向上する。Acrylic elastic polymer (B) used in the present invention
is a copolymer with a copolymerizable monomer such as methacrylic ester, butadiene, styrene, or acrylonitrile containing acrylic ester as the main component. -ethylhexyl acrylate, n-butyl acrylate, etc.) 40-95% by weight and butadiene 5-40mff
1% and methyl methacrylate 0-30% by weight and 0.0
A mixed monomer consisting of 1 to 3% by weight of a crosslinking agent (for example, ethylene dimethacrylate, etc.) is emulsion polymerized, and a flocculant is added to this to obtain a crosslinked rubber with an average calibration diameter of OJ ~ 0.3μ. First, 20-80% by weight of styrene and 20-80% by weight of methyl methacrylate are added to a latex containing 50-80 parts by weight of a polymer.
50!1ffi% and acrinitrile O~60Jij1
% and im agent (e.g., ethylene dimethacrylate, divinylbenzene, etc.), 0.1 to 2 m [m%] after addition and polymerization of 10 to 40 parts by weight of monomer, crosslinking agent (e.g., ethylene dimethacrylate, divinylbenzene, etc.). etc.) 0.1
-4% by weight of alkyl methacrylates whose alkyl group has 1 to 4 carbon atoms (e.g. methyl methacrylate, etc.) 5 to 4% by weight
It is a multi-component resin obtained by further adding 25 parts by weight. A specific example of the acrylic elastomeric polymer mentioned above is one commercially available from Kureha Chemical Industry Co., Ltd. under the product name HI-Jin-15. Acrylic elastic polymer (B)
By adding , the tracking properties of polycarbonate are improved.
本発明において使用するガラス繊維は、通i +:Uカ
ーボネートに(更用されるものであれば差支えない。好
ましいガラス繊維は径6〜20μで、成形品中のガラス
繊維の長さは0.05〜0.5mである。又ガラス繊維
は樹脂との4相性を向上させる目的で、シランカップリ
ング剤等の表面処理、取扱注目:同上ざぜる目的でアク
リル糸#脂、ウレタン樹脂等で集束処理が施されてあっ
ても良い。The glass fibers used in the present invention may be of any type as long as they can be used for common i+:U carbonates. The preferred glass fibers have a diameter of 6 to 20μ, and the length of the glass fibers in the molded product is 0. 05 to 0.5m.Glass fibers are surface treated with silane coupling agents, etc., in order to improve their compatibility with the resin, and handling precautions: Same as above, for the purpose of rustling, glass fibers are bundled with acrylic thread #greasy, urethane resin, etc. It may be processed.
本発明の電気機器外かくは前記め3橿の成分を混合、成
形する事によって得られる。混合割合は、芳薔族ポリカ
ーボネート99゜5〜80重量俤、アクリル系弾性重合
体0.5〜20重瓜チからdる組成物100道量部にヌ
ナしてガラス繊維5〜70重量部の範囲である。The outer shell of the electrical equipment of the present invention can be obtained by mixing and molding the three components mentioned above. The mixing ratio is 5 to 80 parts by weight of aromatic polycarbonate, 0.5 to 20 parts by weight of acrylic elastic polymer, and 5 to 70 parts by weight of glass fiber. range.
アクリル系弾性l&体の虞が20重址チを越えると電気
機器外かくの機械的強度が低下し0.5社叔チ禾清では
1トラツキング性の安定性が少ない。またガラス繊維5
重量部未満では電気機器外かくの機械的強度が低下し、
70重量部を越えると成形が困罐である。即ち上記の範
囲の組成物より成形された電気機器外かくけ耐トラツキ
ング性に優れ、また機械的強度、耐熱性、寸法安這性(
も優れている。If the risk of acrylic elasticity exceeds 20 layers, the mechanical strength of the outer shell of the electrical equipment will decrease, and the stability of 1-tracking performance will be low with 0.5 degrees of strength. Also glass fiber 5
If it is less than part by weight, the mechanical strength of the outer shell of electrical equipment will decrease,
If it exceeds 70 parts by weight, molding becomes difficult. In other words, electrical equipment molded from the composition in the above range has excellent tracking resistance when exposed to external scratches, and also has excellent mechanical strength, heat resistance, and dimensional stability (
is also excellent.
本発明の電気機器外殻は、前記の3411の成分を混合
、成形することによって得られる。The electrical device outer shell of the present invention is obtained by mixing and molding the components of 3411 above.
混合および成形には、公知の方法を適用することができ
る。例えば、前記の34I[の成分をタンブラ−1V@
グレンダー、ナウターミキナー等の混合機で混合し、そ
のま〜、或は押出機を通し℃ベレット化して、射出成形
、押出成形、圧縮成形等によって成形される。或は、ポ
リカーボネートとアクリル系弾性重合体の混合物を押出
機のホッパーに供給し、押出機の途中からガラス繊維を
供給して、押出成形しくもよい。その他、種々の混合、
成形手順を実施することが出来る。Known methods can be applied to mixing and shaping. For example, the components of the above 34I [tumbler 1V@
The mixture is mixed in a mixer such as a grinder or a Nautamikiner, and then formed into pellets as they are, or passed through an extruder to form pellets at °C, and then molded by injection molding, extrusion molding, compression molding, or the like. Alternatively, the mixture of polycarbonate and acrylic elastic polymer may be supplied to a hopper of an extruder, and glass fibers may be supplied from the middle of the extruder for extrusion molding. In addition, various mixtures,
A molding procedure can be carried out.
丸に、本発明の目的を損わない範囲内で混合時あるいは
成形時に、ポリエステル、ポリメチルメタアクリレート
等の他の樹脂、炭酸カルシウム、シリカ等の充顛剤ある
I−\(家有効発現鼠の安定剤、酸化防止剤、1色剤、
紫外、環吸収剤等をfBaしても良い。In addition, fillers such as polyester, other resins such as polymethyl methacrylate, calcium carbonate, and silica may be used during mixing or molding within a range that does not impair the purpose of the present invention. stabilizer, antioxidant, one-color agent,
An ultraviolet absorber, a ring absorber, etc. may be used as fBa.
本発明の電気機器外殻は、J I 8(c0702)で
疋めるクラス■の電気a!器に使用することができ、例
えば、磁気のこ、電気ドリル、電気かんな、電気グライ
ンダー尋の外殻が挙げられろ。The outer shell of the electrical equipment of the present invention is a class ■ electric A! Examples include magnetic saws, electric drills, electric planers, and electric grinders.
〈発明の効果〉
かくして覆られる電気機器外かくは、従来の電気機器外
かくに比べ耐トラツキング性が向上し、機械的gL度、
耐熱性等をノくランスよく備え、クラスff電気機器の
外殻としての使用に十分耐えるものである。<Effects of the Invention> The outer cover of the electrical equipment covered in this way has improved tracking resistance compared to the conventional outer cover of electrical equipment, and has improved mechanical gl.
It has excellent heat resistance and can withstand use as the outer shell of class FF electrical equipment.
〈実施例〉
以上実施例を挙げて本発明の詳細な説明する。なお、耐
トラツキング性はI′kJOPublication雪
112に従い、曲げ弾性率はA8’1i−1)−790
(従つ′C測定した。<Examples> The present invention will be described in detail with reference to Examples. In addition, the tracking resistance is according to I'kJOPublication Yuki 112, and the flexural modulus is A8'1i-1)-790.
(Accordingly, 'C was measured.
実施例1〜3
芳香族ポリカーボネート(帝人化或 ■裏:パンライト
L−1250C表中PCで不す)アクリル系弾am合体
(%羽化学工某■; lli人−15)次びガラス礒l
a(日東紡11を表1の#l成に示す割合でグレンダー
で混合した&、30mφベント式押出機(ナカタニ■a
; V8JC−30)を用い、シリンダ一温度300
℃にて押出しベレット化した。このペレットを125℃
で5時間乾燥した後、射出成形機を用(・、シリンダ一
温度320℃、金製温度110℃の条イ牛で、家庭用電
動鋸の)島つンングを成形し、それ力1ら切りとった1
8X18X3.2mの試験片で耐トラツキング性を測定
した。また、同じ条件で6A X 12.7X127s
mの曲げ試験片を成形し、曲げ弾性率を測定した。それ
らの結果を表−!に示す。Examples 1 to 3 Aromatic polycarbonate (Teijin Kagaku Co., Ltd. ■ Back: Panlite L-1250C front with PC inside) Acrylic bullet am combination (% Ha Kagaku Kogyo ■; llijin-15) and then glass powder
a (Nittobo 11 was mixed with a grinder in the proportion shown in #l composition in Table 1 & a 30 mφ vented extruder (Nakatani ■a)
; V8JC-30), cylinder temperature 300
It was extruded into pellets at ℃. This pellet was heated to 125°C.
After drying for 5 hours, use an injection molding machine (using a domestic electric saw with a cylinder temperature of 320°C and a metal wire temperature of 110°C) to form a cylindrical piece, and cut it with force. Ta1
Tracking resistance was measured using a test piece measuring 8 x 18 x 3.2 m. Also, under the same conditions, 6A x 12.7X127s
A bending test piece of m was formed and the bending elastic modulus was measured. Table out those results! Shown below.
比較例1
アクリル系弾性重合体を除いた以外は実施例1と同様の
方法によって、同様の成形品を得、測定した。結果を表
−■に示す。Comparative Example 1 A similar molded article was obtained and measured in the same manner as in Example 1 except that the acrylic elastic polymer was omitted. The results are shown in Table-■.
比較例2
ガラス繊維を除いた以外は実施例2と同様の方法くよっ
て同様の成形品を得、測定した。Comparative Example 2 A similar molded article was obtained in the same manner as in Example 2 except that the glass fibers were removed, and measurements were taken.
結果を表−直にホす。View the results directly.
手続稲正誓 昭和60年1月J日Procedure Ina Sei Oath January J, 1985
Claims (2)
%、(B)アクリル系弾性重合体0.5〜20重量%か
ら成る組成物100重量部に対してガラス繊維を5〜7
0重量部配合して成形されたことを特徴とするクラスI
I電気機器の外殻。(1) 5 to 7 parts by weight of glass fiber to 100 parts by weight of a composition consisting of (A) 99.5 to 80% by weight of aromatic polycarport and (B) 0.5 to 20% by weight of acrylic elastic polymer.
Class I characterized by being molded with 0 parts by weight
I Outer shell of electrical equipment.
範囲第1項記載の電気機器の外殼。(2) The outer shell of an electrical device according to claim 1, wherein the outer shell of the electrical device is a power tool outer shell.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25055484A JPS61130367A (en) | 1984-11-29 | 1984-11-29 | Outer shell of electric equipment |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25055484A JPS61130367A (en) | 1984-11-29 | 1984-11-29 | Outer shell of electric equipment |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS61130367A true JPS61130367A (en) | 1986-06-18 |
Family
ID=17209637
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP25055484A Pending JPS61130367A (en) | 1984-11-29 | 1984-11-29 | Outer shell of electric equipment |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61130367A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6315843A (en) * | 1986-07-07 | 1988-01-22 | Teijin Chem Ltd | Camera part |
-
1984
- 1984-11-29 JP JP25055484A patent/JPS61130367A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6315843A (en) * | 1986-07-07 | 1988-01-22 | Teijin Chem Ltd | Camera part |
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