JPH03215545A - Housing member of office automation appliance - Google Patents
Housing member of office automation applianceInfo
- Publication number
- JPH03215545A JPH03215545A JP1125590A JP1125590A JPH03215545A JP H03215545 A JPH03215545 A JP H03215545A JP 1125590 A JP1125590 A JP 1125590A JP 1125590 A JP1125590 A JP 1125590A JP H03215545 A JPH03215545 A JP H03215545A
- Authority
- JP
- Japan
- Prior art keywords
- vinyl chloride
- resin
- degree
- weight
- chloride resin
- 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
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はオフィスオートメーション(以下OAという)
機器ハクジング部材に関する。[Detailed Description of the Invention] (Industrial Application Field) The present invention is directed to office automation (hereinafter referred to as OA).
The present invention relates to an equipment hacking member.
(従来の技術)
従来より、塩化ビニル樹81は成形品の素材として広く
使用されているが,耐熱性が悪いためOA4lI器ハク
ジング部材として使用した場合、輸送や保管の際に高温
にさらされたり、熱源の周辺で使用されると熱変形する
という欠点があった。この欠点を改良する方法として、
塩化ビニル樹脂を後塩素化する方法が提案されている。(Prior art) Vinyl chloride wood 81 has been widely used as a material for molded products, but because of its poor heat resistance, when used as a breaking material for OA4lI equipment, it may be exposed to high temperatures during transportation or storage. However, they had the disadvantage of being thermally deformed when used near a heat source. As a way to improve this shortcoming,
A method of post-chlorinating vinyl chloride resin has been proposed.
OA機器ハクジング部材は複雑な形状tl!求されるの
で、一般に射出成形されているが塩化ビニル樹脂を後塩
素化すると、樹脂の溶融粘度が高くなり、射出成形しに
〈〈なるという問題がある。OA equipment removal parts have complex shapes! Because of the high demand, injection molding is generally performed, but when vinyl chloride resin is post-chlorinated, the melt viscosity of the resin increases, making injection molding difficult.
そのため、樹脂の重合度を下げたり、樹脂に多量の可塑
剤を添加する等の方法が行われているが、樹脂の重合度
を下けだものでは,力学的物性の低下が著しく、また樹
脂に多量の可塑剤を添加したものでは、樹脂の耐熱性が
著しく損なわれる等の欠点がある。Therefore, methods such as lowering the polymerization degree of the resin or adding a large amount of plasticizer to the resin have been used, but when the polymerization degree of the resin is lowered, the mechanical properties of the resin are significantly reduced, and the resin If a large amount of plasticizer is added to the resin, there are drawbacks such as the heat resistance of the resin being significantly impaired.
又、特開昭55−84347号公報には、塩化ビニル系
樹脂とクルクとアミド化合物よりなる141成物が記載
され、熱安定性と加工性が改良されると記載されている
。しかしながら、タルクほ塩化ビニル樹脂100重量部
に対し20〜30量部と多量に添加されアミド化合物は
1〜3亀量部と少量添加されているためOA機器・・ウ
ジング部材としては耐撃性及び耐衝撃性が不足1〜てい
る。父、塩化ビニル系欄脂として塩素化塩化ビニル樹脂
を使用した際Kは、依然と17で流動性が不足しており
、射出成形すると焼けが生じたり、充填性が不足すると
いう欠点があった。Further, JP-A-55-84347 describes a 141 composition consisting of a vinyl chloride resin, curcum, and an amide compound, and states that it has improved thermal stability and processability. However, since talc is added in a large amount of 20 to 30 parts by weight to 100 parts by weight of vinyl chloride resin, and the amide compound is added in a small amount of 1 to 3 parts by weight, it is not suitable for use as impact resistance or as a housing member for OA equipment. Impact resistance is insufficient. When chlorinated vinyl chloride resin was used as a vinyl chloride-based column resin, K was still 17 and lacked fluidity, resulting in burns during injection molding and poor filling properties. .
(発明が解決しようとするa’M)
本発明の目的は、E紀欠点VCf#iみ、I動特性が良
好であり、従って射出成形性が良好な樹脂組成物を射出
成形して製造された耐熱性、耐衝撃性等のすぐれたOA
機器ハクノング部材を提供−f l)ことVCある。(A'M to be Solved by the Invention) An object of the present invention is to produce a resin composition by injection molding that has good I dynamic characteristics, and therefore good injection moldability. OA with excellent heat resistance, impact resistance, etc.
There is a VC that provides equipment components.
(課題を解決するための手段)
塩素化度が62〜681量%のものである。塩素化度が
62恵量%未膚の塩素化塩化ビニル樹脂では、該摺脂の
耐熱性は塩化ビニル#1脂(塩素化度約57!量%)と
さほど変わりはなく、また塩素化度が68!量%を超え
る塩素化塩化ビニル樹脂は熱分解し易くなるからである
。また、塩素化塩化ビニル樹脂の亀合度は400〜80
0′″Cある。塩素化塩化ビニル樹脂の恵今度が400
未満の場合には、得られるハクジング部材の機械的強度
が低下し、塩素化塩化ピニル檎脂の塩合度が800を超
えると、配合物の流動特性が低下し、射出成形性が悪く
なるからである。(Means for solving the problem) The degree of chlorination is 62 to 681% by weight. For chlorinated vinyl chloride resin with a chlorination degree of 62%, the heat resistance of the resin is not much different from vinyl chloride #1 resin (chlorination degree of about 57%), and is 68! This is because chlorinated vinyl chloride resin exceeding the amount of % is likely to be thermally decomposed. In addition, the degree of chlorinated vinyl chloride resin is 400 to 80.
There is 0'''C. Ekima of chlorinated vinyl chloride resin is 400
If the degree of salinity of the chlorinated pinyl chloride fat exceeds 800, the flow characteristics of the compound will decrease and the injection moldability will deteriorate. be.
本発明で用いるビスアミド化合物(bl fl一般式(
Ilでボされる化合物であり,
( R CONH )2 ( C H!) n −
(I)式中,Rは炭素数12〜23のアルキル基又は該
アルキル基の水素が水酸基で置換されたアルキル基を示
し、nは1〜10の!1敗を示す。Rの炭素数が24以
上もし< tl nが11以上になると配合物のゲル化
時間が長くなり、塩素化塩化ビニル樹脂が熱分解しやす
くなる。Bisamide compound used in the present invention (bl fl general formula (
It is a compound represented by Il, (RCONH)2(CH!)n-
In formula (I), R represents an alkyl group having 12 to 23 carbon atoms or an alkyl group in which the hydrogen of the alkyl group is substituted with a hydroxyl group, and n is 1 to 10! Indicates 1 loss. If the number of carbon atoms in R is 24 or more, < tl n is 11 or more, the gelation time of the compound becomes longer and the chlorinated vinyl chloride resin becomes more susceptible to thermal decomposition.
上記ビスアミド化合物tblとしては、たとえばメチレ
ンビスステアリン駿アミド、エチレンビスカブリン酸ア
ミド、エチレンビスラクリル醒アミド、エチレンビスス
テアリン酸アミド、エチレンビスイソステアリン醍アミ
ト゛、エチレンビス(12−ヒドロキシ)ステアリン綬
アミド、エチレンビスベヘンHy=ド、ヘキサメチレン
ピスステアリン酸アミド、ヘキサメチレンビス(12−
ヒドロキシ)ステアリン峻アミド、ヘキサメチレンビス
ベヘン醍アミF等がめげられ、単独または二種以上が併
用されてもよい。Examples of the above-mentioned bisamide compound tbl include methylene bisstearin amide, ethylene biscarinamide, ethylene biscrarylic amide, ethylene bis stearic acid amide, ethylene bis isostearin amide, ethylene bis (12-hydroxy) stearin amide, Ethylene bisbehene Hy=do, hexamethylene pistearic acid amide, hexamethylene bis(12-
Hydroxy) stearin amide, hexamethylene bisbehen amide F, etc. may be used alone or in combination of two or more.
本発明で用いる衝撃改良剤(c) I′i、一般Kjj
i化ビニル系檎脂用の改質剤として使用されているゴム
代分であり,たとえばMBS横脂、ABS檎脂、塩素化
ポリエチレン等があけられる。Impact modifier (c) I′i used in the present invention, general Kjj
It is a rubber component used as a modifier for i-vinyl resin, such as MBS side resin, ABS resin, chlorinated polyethylene, etc.
本発明の配合物は上記塩素化塩化ビニル欄脂(a),ビ
スアミド系化合物ib)及ひ衝撃改艮剤Lclからなる
が、ビスアミド系化合物(blの添加量は少ないと射出
成形性を向上させる幼来がなく、多くなると耐熱性、力
学物性等が低下し、又、衝撃改良剤(clの添加量が少
なくなると成形品の耐衝撃性が低下し、多くなると力学
物性が低下するので、塩素化塩化ビニル樹脂100亀量
部に対し、ビスアミド系化合物tb)は4〜15重量部
添加さh.衝撃改良剤(c)n5〜20重量部添加され
る。The composition of the present invention consists of the above-mentioned chlorinated vinyl chloride resin (a), bisamide compound ib), and impact modifier Lcl, but injection moldability is improved if the amount of bisamide compound (bl) added is small. If the amount of Cl added decreases, the impact resistance of the molded product will decrease, and if the amount increases, the mechanical properties will decrease. To 100 parts by weight of the vinyl chloride resin, 4 to 15 parts by weight of the bisamide compound (tb) is added, h. 5 to 20 parts by weight of the impact modifier (c) is added.
本発明のOA&器ハクジング部材は上記配合物を射出成
形して得られたものであるがOA機器ハクジング部材は
一般に耐候性が要求されるので紫外線吸収剤が添加され
るのが好ましい。The OA/equipment removal member of the present invention is obtained by injection molding the above-mentioned compound, and since OA equipment removal members are generally required to have weather resistance, it is preferable to add an ultraviolet absorber.
紫外線吸収剤としては、たとえばサリチル酸エステノ冫
系、ペンゾフエノン系、サリシレート系、ペンゾトリア
ゾール系等の紫外線吸収剤があけられ、その添加量は塩
素化塩化ビニル樹脂100重量部に対し0.05〜α5
菖量部である。As the ultraviolet absorber, for example, salicylic acid ester, penzophenone, salicylate, penzotriazole, and other ultraviolet absorbers are used, and the amount added is 0.05 to α5 per 100 parts by weight of chlorinated vinyl chloride resin.
This is the irises section.
又、さらに、必要KF6してステアリン酸,モンクン峻
ワックス等の滑剤、ステアリン峻鉛,ステアリン醒カル
ンクム、ジプチル錫ジマレー}・等の熱安定剤、抗酸化
剤、ガラス繊維、炭駿カルンクム、タルク等の充填剤、
顔料、着色剤、加工助剤等ft浜加レてもよい。In addition, necessary KF6, lubricants such as stearic acid and moncoal wax, heat stabilizers such as stearic acid, stearic acid caruncum, diptyltin dimale}, antioxidants, glass fibers, charcoal caruncum, talc, etc. filler,
Pigments, colorants, processing aids, etc. may also be used.
上記配合物の製造方法は任意の方法が採用されてよく、
たとえば塩素化塩化ビニル樹脂tal、ビスアミド系化
合物(bl及び衝撃改良剤(clをスパーミキサー.プ
レンダー等に供給し、撹拌混合すればよい。Any method may be used to produce the above-mentioned compound,
For example, chlorinated vinyl chloride resin tal, bisamide compound (BL) and impact modifier (CL) may be supplied to a spar mixer, blender, etc., and mixed with stirring.
L記配合物f:射出収形してOA機器ハウジング部材t
−得るには、公知の任意の射出成形が採用されてよく,
パレル温度160〜200℃で射出成形されるのが好ま
しい。L compound f: injection molded OA equipment housing member t
- Any known injection molding method may be employed to obtain the
Preferably, injection molding is performed at a parel temperature of 160 to 200°C.
(実施例) 次に本発明の実施例を説明する。(Example) Next, embodiments of the present invention will be described.
実施例1〜5、比較例1〜3
第1表に下l7た所定量の塩素化塩化ビニル樹脂(1合
度500,塩素化度651目).ピスアミド化合物、M
BSm脂(呉羽化学社製、BTA−mN)Mびに紫外線
吸収剤(2−ヒドロキノー4−n−オクチルベンゾ■エ
ノン、共同薬品社製バイオソーグ130)及びジオクチ
ル錫メルカグト(日東化成社ITVs−8831)21
i量部,ジオクチル錫マレートボリマー(LJLNI[
社%!TVS−8 8 L 3 ) 1!量部、滑剤(
ヘキストジャバン社製,WAX−OP )l亜量部並び
に酸化チタン(帝国化工社11JR−403)37@@
部をヘンシエルミキサーに供給し、80℃で5分園混合
して配合物を得た。Examples 1 to 5, Comparative Examples 1 to 3 Predetermined amounts of chlorinated vinyl chloride resins (1 degree: 500, chlorination degree: 651) shown in Table 1. Pisamide compound, M
BSm fat (manufactured by Kureha Kagaku Co., Ltd., BTA-mN), ultraviolet absorber (2-hydroquino 4-n-octylbenzoenone, Kyodo Yakuhin Co., Ltd. Biosorg 130) and dioctyltin mercagut (Nitto Kasei Co., Ltd. ITVs-8831) 21
i parts, dioctyltin malate polymer (LJLNI [
Company%! TVS-8 8 L 3) 1! Quantity part, lubricant (
Manufactured by Hoechst Javan Co., Ltd., WAX-OP) l subunit and titanium oxide (Teikoku Kakosha 11JR-403) 37@@
The mixture was fed into a Henschel mixer and mixed for 5 minutes at 80°C to obtain a blend.
得られた配合物を二軸混練押出機に供給し、最高温度1
90℃で混練、押出し、ペレタイザーによってベレット
化した。得られたベレットをOAハクジング用金型の投
置された射出成形機(東芝機械■Is−850E)に供
給し,射出圧力1840即/一、成形温度170〜18
0℃、スクリュー回転数6 0 rpm s金型温度3
0℃、の射出条件で縦400fi、横600M、厚さ3
を観察し、結果を第1表に示した。The obtained mixture was fed to a twin-screw kneading extruder, and the maximum temperature was 1.
The mixture was kneaded at 90°C, extruded, and pelletized using a pelletizer. The obtained pellet was fed to an injection molding machine (Toshiba Machine Is-850E) equipped with an OA hacking mold, and the injection pressure was 1840/1 and the molding temperature was 170-18.
0°C, screw rotation speed 6 0 rpm s mold temperature 3
Under injection conditions of 0°C, length: 400fi, width: 600M, thickness: 3
were observed, and the results are shown in Table 1.
上記配合物を高化式フローテスター(ダイlO m X
1 m 125 ) K供給し、190℃、160即
/dの条件で熔融粘度を測定し,結果を第1麦に示した
。The above formulation was tested using a Koka type flow tester (Dylom
1 m 125 ) K was supplied, and the melt viscosity was measured under the conditions of 190° C. and 160 instant/d, and the results were shown in the first barley.
父、得られた板状体を切断し、190℃でプレス成形l
2、プレス板を得、得られた厚さ6.2頗のプレス板を
用いてJ I S−K7 207 (18.5K9/c
lilt:準じて耐熱性(HDT)を測定し、得られた
厚さ4關のプレス体を用いてJIS−K7111に準じ
てンヤルビー衝撃強度を測定し、vAl麦に示した。The obtained plate-like body was cut and press-formed at 190°C.
2. Obtain a press plate and use the obtained press plate with a thickness of 6.2 mm to make JIS-K7 207 (18.5K9/c
lilt: The heat resistance (HDT) was measured according to the method, and the Nyaruby impact strength was measured according to JIS-K7111 using the obtained press body with a thickness of 4 mm, and the results are shown in vAl barley.
父、得られた板状体を、耐色試験用水銀ランプ(JIS
C 7709 E39指定)を有する照射装置
(水平距離)K供給し、JISK5400 (色の安定
性)に準拠し、100時間後の黄変性を目視にてFJ定
し、結果全第1麦に小した。My father used a mercury lamp for color fastness testing (JIS
An irradiation device (horizontal distance) with a C7709 E39 designation) was supplied, and the yellowing after 100 hours was visually determined in accordance with JIS K5400 (color stability). .
(以下余白)
第
l
麦
ωEBSA :エチレンビスステアリン酸アミドEB
HSA:エチレンビス(12〜ヒドロキン)ステアリン
酸アミEBBA :エチレンビスベヘン酸アミトHB
SA :ヘキサメチレンビスステアリ/醒アミドSG
E :七ノステアリン酸グリセライドド
(発明の勿果)
本発明のOA機器・・クジング部材の構成は上述の通り
であり、特定の塩素化塩化ビニル檎脂に多量のビスアミ
ド化合物と衝撃改良剤が添加された配合物が射出成形さ
れて成形されているので、流動特性がすぐれており、射
出成形の際に剪断発熱が小さく、充填性よく成形でき、
ハクジング部材のk面にヤクやフローマークが入らず外
観がきれいであり、かつ耐熱性、耐衝撃性がすぐれてお
り、コンピュータのキャビネント、キーボード等のOA
機器ハウジング部材として好適に使用できる。(Left below) No. 1 Wheat ωEBSA: Ethylene bisstearamide EB
HSA: Ethylene bis(12-hydroquine) stearic acid amide EBBA: Ethylene bis behenic acid amide HB
SA: Hexamethylene bisstearyl/Sameamide SG
E: Heptanostearic acid glyceride (result of the invention) The composition of the OA equipment/cushion member of the present invention is as described above, and a large amount of bisamide compound and impact modifier are added to a specific chlorinated vinyl chloride resin. Since the added compound is molded by injection molding, it has excellent flow characteristics, generates little shear heat during injection molding, and can be molded with good filling properties.
It has a clean appearance with no stains or flow marks on the surface of the breaking part, and has excellent heat resistance and impact resistance, making it suitable for office equipment such as computer cabinets and keyboards.
It can be suitably used as a device housing member.
Claims (1)
0〜800の塩素化塩化ビニル樹脂100重量部、 (b)一般式( I )で示されるビスアミド系化合物4
〜15重量部及び (RCONH)_2(CH_3)_n……( I ) (式中Rは炭素数12〜23のアルキル基又は該アルキ
ル基の水素が水酸基で置換されたアルキル基を示し、n
は1〜10の整数を示す。) (c)衝撃改良剤5〜20重量部 よりなる配合物が射出成形されてなるオフィスオートメ
ーション機器ハウジング部材。[Claims] 1. (a) The degree of chlorination is 62 to 68% by weight and the degree of polymerization is 40.
100 parts by weight of a chlorinated vinyl chloride resin having a molecular weight of 0 to 800, (b) a bisamide compound represented by the general formula (I) 4
~15 parts by weight and (RCONH)_2(CH_3)_n...(I) (In the formula, R represents an alkyl group having 12 to 23 carbon atoms or an alkyl group in which the hydrogen of the alkyl group is substituted with a hydroxyl group, and n
represents an integer from 1 to 10. ) (c) An office automation equipment housing member formed by injection molding a formulation comprising 5 to 20 parts by weight of an impact modifier.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1125590A JPH03215545A (en) | 1990-01-20 | 1990-01-20 | Housing member of office automation appliance |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1125590A JPH03215545A (en) | 1990-01-20 | 1990-01-20 | Housing member of office automation appliance |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH03215545A true JPH03215545A (en) | 1991-09-20 |
Family
ID=11772832
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1125590A Pending JPH03215545A (en) | 1990-01-20 | 1990-01-20 | Housing member of office automation appliance |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH03215545A (en) |
-
1990
- 1990-01-20 JP JP1125590A patent/JPH03215545A/en active Pending
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP4755399B2 (en) | Flame retardant styrene resin composition | |
| KR20130043231A (en) | Heat-stabilized polyamide composition | |
| JPS6157641A (en) | Fluorinated thermoplastic elastomer composition | |
| JPH05132602A (en) | Chlorinated pvc blend | |
| US8138241B2 (en) | Shapable resin compositions | |
| HUE027956T2 (en) | Expandable granules based on vinyl aromatic polymers with improved expandability; and a method for producing them | |
| WO2004083301A1 (en) | Cellulose reinforced resin compositions | |
| JP6942233B1 (en) | Resin composition and molded product | |
| US7645819B2 (en) | Extrudable PVC compositions | |
| JPH03215545A (en) | Housing member of office automation appliance | |
| JPH0344105B2 (en) | ||
| JP6941725B1 (en) | Resin composition | |
| JPH08302129A (en) | Vinyl chloride resin composition | |
| JPH06263948A (en) | Flame-retardant resin composition | |
| JP2021195530A (en) | Styrenic resin composition | |
| KR100430194B1 (en) | Resin composition with greatly improved processing and extrusion stability | |
| JPH043425B2 (en) | ||
| JPH03149246A (en) | Production of vinyl chloride resin composition | |
| Bilgiç | Processing of PVC | |
| JPH03152148A (en) | Rigid chlorinated vinyl chloride-based resin composition for extrusion molding | |
| EP0467368A2 (en) | Secondary amides in polyethylene terepthalate molding compositions | |
| JPH03152147A (en) | Rigid chlorinated vinyl chloride-based resin composition for injection molding | |
| JPH03152146A (en) | Rigid chlorinated vinyl chloride-based resin composition for blow molding | |
| JPH07224198A (en) | Polystyrene resin composition | |
| JP2001002947A (en) | Flame-retardant resin composition |