JPH07124997A - Outsert molded article - Google Patents
Outsert molded articleInfo
- Publication number
- JPH07124997A JPH07124997A JP27554993A JP27554993A JPH07124997A JP H07124997 A JPH07124997 A JP H07124997A JP 27554993 A JP27554993 A JP 27554993A JP 27554993 A JP27554993 A JP 27554993A JP H07124997 A JPH07124997 A JP H07124997A
- Authority
- JP
- Japan
- Prior art keywords
- resin
- outsert
- formal
- copolymer resin
- molded article
- 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
- 229930182556 Polyacetal Natural products 0.000 claims abstract description 22
- 229920006324 polyoxymethylene Polymers 0.000 claims abstract description 22
- 238000002425 crystallisation Methods 0.000 claims abstract description 14
- 230000008025 crystallization Effects 0.000 claims abstract description 14
- 229920006026 co-polymeric resin Polymers 0.000 claims abstract description 13
- 238000000465 moulding Methods 0.000 claims abstract description 12
- 229920000642 polymer Polymers 0.000 claims abstract description 12
- 125000005702 oxyalkylene group Chemical group 0.000 claims abstract description 6
- 125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 claims abstract description 6
- 239000000155 melt Substances 0.000 claims abstract description 4
- 239000000758 substrate Substances 0.000 claims description 7
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims description 3
- AUAGGMPIKOZAJZ-UHFFFAOYSA-N 1,3,6-trioxocane Chemical compound C1COCOCCO1 AUAGGMPIKOZAJZ-UHFFFAOYSA-N 0.000 claims description 2
- VDFVNEFVBPFDSB-UHFFFAOYSA-N 1,3-dioxane Chemical compound C1COCOC1 VDFVNEFVBPFDSB-UHFFFAOYSA-N 0.000 claims description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 2
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 claims description 2
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 2
- 239000000178 monomer Substances 0.000 claims description 2
- 229920005989 resin Polymers 0.000 abstract description 37
- 239000011347 resin Substances 0.000 abstract description 37
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 229920006351 engineering plastic Polymers 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 2
- 125000006353 oxyethylene group Chemical group 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C45/00—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
- B29C45/14—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor incorporating preformed parts or layers, e.g. injection moulding around inserts or for coating articles
- B29C45/14336—Coating a portion of the article, e.g. the edge of the article
- B29C45/14344—Moulding in or through a hole in the article, e.g. outsert moulding
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明はアウトサート成形品に係
わり、特に精密でかつ優れた寸法安定性が要求される用
途に好適に用いられるアウトサート成形品に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an outsert molded product, and more particularly to an outsert molded product suitable for use in applications requiring precision and excellent dimensional stability.
【0002】[0002]
【従来の技術】テープレコーダー、ビデオテープレコー
ダー(VTR)のシャーシ類に代表される各種シャーシ
やスイッチ基板等は、設計の自由度が大きい事、後加工
が削減できる事、軽量化が図れる事、安価である事等の
利点から、金属製等の硬質基板と熱可塑性樹脂を一体化
してなるアウトサート成形品が広く使用されている。こ
れらのアウトサート成形用の熱可塑性樹脂としては、ポ
リエチレン、ポリプロピレン等のポリオレフィン樹脂を
はじめ、ポリエステル樹脂、ポリアセタール樹脂、ポリ
アミド樹脂、ポリカーボネート樹脂等のエンジニアリン
グプラスチック等、種々のものが使用されている。特に
精密で寸法安定性が要求される用途には、前記のエンジ
ニアリングプラスチックが使用されており、とりわけテ
ープレコーダー、VTR等のシャーシには、剛性、クリ
ープ特性、摺動特性の優れたポリアセタール樹脂が広く
使用されている。2. Description of the Related Art Various chassis such as tape recorders and video tape recorder (VTR) chassis, switch boards, and the like have a large degree of freedom in designing, post-processing can be reduced, and weight can be reduced. Outsert moldings in which a hard substrate made of metal or the like and a thermoplastic resin are integrated are widely used because of their advantages such as low cost. As these thermoplastic resins for outsert molding, various resins such as polyolefin resins such as polyethylene and polypropylene as well as engineering plastics such as polyester resins, polyacetal resins, polyamide resins and polycarbonate resins are used. The engineering plastics mentioned above are used for applications that require particularly high precision and dimensional stability. Especially for chassis such as tape recorders and VTRs, polyacetal resin with excellent rigidity, creep properties and sliding properties is widely used. It is used.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、ポリア
セタール樹脂はクリープ特性を初めとする優れた機械的
物性、電気特性、摺動特性を有しているが、成形時の収
縮が大きく、金属或いは熱硬化性樹脂等からなる硬質の
基板との気密性、密着性が悪くなる問題がある。また、
成形品を高温雰囲気に置いた場合にはポリアセタール樹
脂の後収縮により気密性、密着性が悪くなったり、樹脂
製機能部品乃至樹脂製機能部品間を結ぶランナー部に割
れが発生したり、甚だしくは機能部にも割れが発生する
という問題がある。ランナー部の割れを防止する方法と
しては、ランナー部にS字型の部分を設け、応力を吸
収、分散させる機構を付与する方法等が用いられている
が、成形品の設計に制約がでる問題がある。However, although the polyacetal resin has excellent mechanical properties such as creep properties, electrical properties, and sliding properties, it has a large shrinkage at the time of molding, and it is hard to cure with metal or heat. There is a problem in that the airtightness and adhesion to a hard substrate made of a flexible resin deteriorates. Also,
If the molded product is placed in a high temperature atmosphere, the airtightness and adhesion will deteriorate due to the post-shrinkage of the polyacetal resin, cracks will occur in the resin functional parts and the runners connecting the resin functional parts, and There is a problem that the functional part is also cracked. As a method of preventing cracking of the runner part, a method of providing an S-shaped part on the runner part and adding a mechanism for absorbing and dispersing stress is used, but there is a problem in designing the molded product. There is.
【0004】[0004]
【課題を解決するための手段】本発明者等は、かかる従
来技術の問題点を解消して、硬質基板と樹脂部品間の気
密性、密着性を改良し、高温又は低温の雰囲気に置いた
場合も樹脂部品や樹脂ランナー部に亀裂、割れが発生す
る事を防止し、良好なアウトサート成形品を提供する事
を目的に鋭意検討した結果、特定のポリアセタール共重
合樹脂を用いる事が極めて有効であることを見出し、本
発明を完成するに到った。DISCLOSURE OF THE INVENTION The inventors of the present invention have solved the problems of the prior art, improved the airtightness and adhesion between the hard substrate and the resin parts, and placed them in a high temperature or low temperature atmosphere. Also in the case, as a result of diligent study to prevent the occurrence of cracks and cracks in resin parts and resin runners and to provide good outsert molded products, it is extremely effective to use a specific polyacetal copolymer resin. Therefore, the present invention has been completed.
【0005】即ち本発明は、少なくとも一つ以上の切欠
きもしくは穴のあいた硬質基板に結晶化時間が5分以上
のポリアセタール共重合樹脂の機能部をアウトサート成
形法により形成したアウトサート成形品である。That is, the present invention is an outsert molded article in which a functional portion of a polyacetal copolymer resin having a crystallization time of 5 minutes or more is formed on a hard substrate having at least one notch or hole by an outsert molding method. is there.
【0006】本発明でいう結晶化時間とは、示差走査熱
量計(以下DSCという)を用いて、ポリアセタール樹
脂を 200℃で5分間保持した後、10℃/分で 152℃まで
降温し、 152℃で保持したときの保持開始から結晶化に
よる発熱ピークまでの時間を言い、時間が短いものほど
結晶化速度は速い事を意味する。The crystallization time referred to in the present invention means that the polyacetal resin is held at 200 ° C. for 5 minutes by using a differential scanning calorimeter (hereinafter referred to as DSC), and then the temperature is lowered to 152 ° C. at 10 ° C./minute. It means the time from the start of holding when kept at ℃ to the exothermic peak due to crystallization, and the shorter the time, the faster the crystallization rate.
【0007】本発明では、この結晶化時間が5分以上で
あるポリアセタール共重合樹脂が選択的に使用される。
優れたアウトサート成形品を得るには、使用する樹脂材
料の結晶化時間が重要であり、結晶化時間が5分より短
いと、成形時の収縮および成形品を加熱した時の後収縮
が大きいため、本発明所期の効果が得られない。逆に結
晶化時間があまりにも長過ぎると射出された樹脂の固化
時間が長くなり生産性が低下するばかりか、得られた成
形品の機械品強度が低下するため好ましくなく、実用的
には5〜200 分の範囲が好ましい。In the present invention, the polyacetal copolymer resin having the crystallization time of 5 minutes or more is selectively used.
In order to obtain an excellent outsert molded product, the crystallization time of the resin material used is important. If the crystallization time is shorter than 5 minutes, the shrinkage during molding and the post-shrinkage when the molded product is heated are large. Therefore, the intended effect of the present invention cannot be obtained. On the contrary, if the crystallization time is too long, not only the solidification time of the injected resin becomes long and the productivity is lowered, but also the mechanical strength of the obtained molded article is lowered, which is not preferable and practically 5 A range of up to 200 minutes is preferred.
【0008】本発明のポリアセタール樹脂とは、オキシ
メチレンユニット(-OCH2-)を主たる構成単位とし、下記
に示す環状エーテルもしくは環状ホルマール等を共重合
させて得られるコポリマーもしくはターポリマーを含む
共重合体である。また、ポリマーの骨格については特に
限定されず、線状のみならず分岐構造、架橋構造を有す
るものであってもなんら問題はない。The polyacetal resin of the present invention means a copolymer containing a oxymethylene unit (-OCH 2- ) as a main constituent unit and a copolymer or terpolymer obtained by copolymerizing the following cyclic ether or cyclic formal. It is united. Further, the skeleton of the polymer is not particularly limited, and there is no problem even if it has not only a linear structure but also a branched structure or a crosslinked structure.
【0009】又、かかるポリアセタール樹脂のメルトイ
ンデックス(以下MIという)については、特に限定さ
れないが、成形性の点から 1.0〜60g/10分である事が
望ましい。MIが 1.0より小さいと、射出成形の際、樹
脂の流動が悪く所望する形状の成形品が得にくくなる。
一方、MIが大きすぎると成形品が脆くなり好ましくな
い。尚、本発明で言うメルトインデックスとは、AST
M−D1238により、 190℃、2160gの荷重で測定した値
でg/10分の単位で表されるものである。The melt index (hereinafter referred to as MI) of the polyacetal resin is not particularly limited, but is preferably 1.0 to 60 g / 10 minutes from the viewpoint of moldability. When the MI is less than 1.0, the resin does not flow well during injection molding, and it becomes difficult to obtain a molded product having a desired shape.
On the other hand, if the MI is too large, the molded product becomes brittle, which is not preferable. The melt index referred to in the present invention is AST.
According to MD-1238, the value measured at a temperature of 190 ° C. and a load of 2160 g is expressed in units of g / 10 minutes.
【0010】ポリアセタールコポリマーの製造に用いる
コモノマー成分は特に限定されないが、一般的には下記
した一般式の構造を有するものから選ばれた少なくとも
1種以上であることが好ましい。The comonomer component used for producing the polyacetal copolymer is not particularly limited, but it is generally preferable to be at least one selected from those having a structure of the following general formula.
【0011】[0011]
【化1】 [Chemical 1]
【0012】(但し、R1、R2、R3、R4は、同一又は異な
る置換基であり、水素原子、アルキル基(1〜5個の炭
素を有し0〜3個の水素がハロゲン原子で置換されたも
の、以下同じ)、または、ハロゲンで置換されたアルキ
ル基を意味し、R5はメチレン基、オキシメチレン基、夫
々アルキル基もしくはハロゲン化アルキルで置換された
メチレン基もしくはオキシメチレン基(この場合、p=
0〜3の整数)、-(CH2)q -OCH2-(q =1〜4の整数)
または-(O-CH2-CH2)q -OCH2-(q =1〜4の整数)で示
される2価の基(この場合p=1)を示す。)また、上
記の如き結晶化時間が5分以上の共重合体とするために
は、オキシメチレンユニットを主たる構成単位とする重
合体中に炭素数2以上のオキシアルキレンユニットを3
〜30mol %、好ましくは3〜15mol %含有するもの、特
に炭素数2以上のオキシアルキレンユニットを構成する
モノマー成分が、1,3 −ジオキソラン、ジエチレングリ
コールホルマール、1,3 −プロパンジオールホルマー
ル、1,4 −ブタンジオールホルマール、1,5 −ペンタン
ジオールホルマール及び1,6 −ヘキサンジオールホルマ
ールの何れか1種以上であることが望ましい。(Wherein R 1 , R 2 , R 3 and R 4 are the same or different substituents, and are a hydrogen atom, an alkyl group (having 1 to 5 carbons and 0 to 3 hydrogens being halogens). Atom-substituted, the same shall apply hereinafter) or a halogen-substituted alkyl group, and R 5 represents a methylene group, an oxymethylene group, a methylene group or an oxymethylene group substituted by an alkyl group or an alkyl halide, respectively. Group (in this case p =
Integer of 0 to 3), - (CH 2) q -OCH 2 - (q = 1~4 integer)
Or - a divalent group represented by (q = 1 to 4 integer) (in this case p = 1) - (O- CH 2 -CH 2) q -OCH 2. ) Further, in order to obtain a copolymer having a crystallization time of 5 minutes or more as described above, 3 oxyalkylene units having 2 or more carbon atoms are added to a polymer having an oxymethylene unit as a main constituent unit.
To 30 mol%, preferably 3 to 15 mol%, in particular, the monomer component constituting the oxyalkylene unit having 2 or more carbon atoms is 1,3-dioxolane, diethylene glycol formal, 1,3-propanediol formal, 1,4 It is desirable to use at least one of butanediol formal, 1,5-pentanediol formal, and 1,6-hexanediol formal.
【0013】尚、本発明は、従来公知の添加剤、例え
ば、酸化防止剤をはじめとする各種安定剤、核剤、顔
料、帯電防止剤等や、耐光安定剤、強化材料、例えば、
ガラスファイバー、ガラスフレーク、タルク、マイカ、
チタン酸カリウイスカー等を添加、配合する事ができ
る。その他、ポリウレタン樹脂、アクリル樹脂、ポリオ
レフィン樹脂等とのポリマーブレンド、ポリマーアロイ
も可能である。The present invention is based on conventionally known additives such as various stabilizers including antioxidants, nucleating agents, pigments, antistatic agents, light stabilizers and reinforcing materials such as
Glass fiber, glass flakes, talc, mica,
Potassium titanate whiskers can be added and blended. In addition, polymer blends with polyurethane resins, acrylic resins, polyolefin resins, etc., and polymer alloys are also possible.
【0014】[0014]
【作用】結晶化時間が5分以上のポリアセタール共重合
樹脂は、優れた機械的強度、耐熱性、摺動性を有するだ
けでなく、成形時の収縮、後加熱による収縮が小さく優
れた寸法安定性を示すので、特に精密で寸法安定性が要
求されるシャーシ類のアウトサート成形用に最適な樹脂
材料となり、金属部品あるいは熱硬化性樹脂等の部品と
ポリアセタール共重合樹脂製部品間の気密性、密着性に
優れ、長期にわたって、亀裂、割れが極めて少ない優れ
たアウトサート成形品を得る事ができる。[Function] The polyacetal copolymer resin having a crystallization time of 5 minutes or more has not only excellent mechanical strength, heat resistance and slidability, but also small shrinkage during molding and shrinkage due to post-heating and excellent dimensional stability. Since it exhibits excellent properties, it becomes an optimal resin material for outsert molding of chassis that requires particularly precise and dimensional stability, and airtightness between metal parts or thermosetting resin parts and polyacetal copolymer resin parts In addition, it is possible to obtain an excellent outsert molded product which is excellent in adhesion and has few cracks and cracks over a long period of time.
【0015】[0015]
【実施例】以下、本発明を実施例により詳細に説明する
が、本発明がこれらに限定されるものではない事は勿論
である。EXAMPLES The present invention will now be described in detail with reference to Examples, but it goes without saying that the present invention is not limited to these.
【0016】実施例1 コポリマー成分として、1,3 −ジオキソランからなるオ
キシアルキレンユニットを3重量%含有するポリアセタ
ール共重合樹脂を用い、射出成形機にて図1に示す成形
品を成形した。得られた成形品を温度23℃、相対湿度50
%に調整された部屋で24時間放置した後、アウトサート
された金属部材と樹脂ボス部の固着の度合い(ガタツキ
の程度)及び樹脂部のクラック、割れの有無を調べた。
又、この成形品のヒートショック試験を行った後、金属
部品と樹脂ボス部の固着の度合い(ガタツキの程度)及
び樹脂部の亀裂、割れの有無を調べた。これらの結果を
表1に示す。Example 1 As a copolymer component, a polyacetal copolymer resin containing 3% by weight of an oxyalkylene unit composed of 1,3-dioxolane was used to mold a molded product shown in FIG. 1 with an injection molding machine. The molded product obtained is at a temperature of 23 ° C and a relative humidity of 50.
After being left for 24 hours in a room adjusted to 100%, the degree of sticking (degree of rattling) between the outsert metal member and the resin boss portion and the presence or absence of cracks or breaks in the resin portion were examined.
Further, after performing a heat shock test on this molded product, the degree of fixation (the degree of rattling) between the metal part and the resin boss portion and the presence or absence of cracks or cracks in the resin portion were examined. The results are shown in Table 1.
【0017】ヒートショック試験とは成形品を 120℃で
1時間加熱した後、すぐに−40℃の雰囲気に成形品を移
して1時間冷却する試験であり、加熱−冷却を1サイク
ルとして、100 サイクルの試験を行った。The heat shock test is a test in which a molded product is heated at 120 ° C. for 1 hour and then immediately transferred to an atmosphere of −40 ° C. and cooled for 1 hour. The cycle was tested.
【0018】実施例2 トリオキサンと1,3 −ジオキソランの混合比率を変えた
以外は実施例1と同様の操作を行いオキシエチレンユニ
ットが5重量%の重合体を作製した。この重合体を用い
た場合についても実施例1と同様の試験を行った。これ
らの結果を表1に示す。Example 2 A polymer having 5% by weight of oxyethylene units was prepared in the same manner as in Example 1 except that the mixing ratio of trioxane and 1,3-dioxolane was changed. The same test as in Example 1 was carried out also when this polymer was used. The results are shown in Table 1.
【0019】実施例3 1,3 −ジオキソランを1,4 −ブタンジオールホルマール
に変えた以外は実施例1と同様の操作を行いオキシブチ
レンユニットが4重量%の重合体を作製した。この重合
体を用いた場合についても実施例1と同様の試験を行っ
た。これらの結果を表1に示す。Example 3 A polymer having an oxybutylene unit of 4% by weight was prepared in the same manner as in Example 1 except that 1,3-dioxolane was changed to 1,4-butanediol formal. The same test as in Example 1 was carried out also when this polymer was used. The results are shown in Table 1.
【0020】比較例1 トリオキサンとエチレンオキシドを一定の混合比率にし
た以外は実施例1と同様の操作を行いオキシエチレンユ
ニットが2.5 重量%の重合体を得た。この重合体を用い
た場合についても実施例1と同様の試験を行った。これ
らの結果を表1に示す。Comparative Example 1 A polymer having 2.5% by weight of oxyethylene units was obtained by the same procedure as in Example 1 except that trioxane and ethylene oxide were mixed at a constant mixing ratio. The same test as in Example 1 was carried out also when this polymer was used. The results are shown in Table 1.
【0021】尚、アウトサート部品(金属部品)と樹脂
部品の固着度合いについては、下記の基準で評価した。The degree of adhesion between the outsert part (metal part) and the resin part was evaluated according to the following criteria.
【0022】○:金属部と樹脂部品間に殆ど隙間がな
く、樹脂部品のがたつきが無いもの ×:金属基板と樹脂部品間に隙間が見られ、樹脂部品の
がたつきが見られるもの 樹脂部品のそり、変形、亀裂、割れの有無を下記の基準
で評価した。○: There is almost no gap between the metal part and the resin part, and there is no rattling of the resin part. ×: There is a gap between the metal substrate and the resin part, and there is rattling of the resin part. The presence or absence of warpage, deformation, cracks and cracks of the resin part was evaluated according to the following criteria.
【0023】○:樹脂部品にそり、変形、亀裂、割れが
ないもの ×:樹脂部品に著しいそりや変形又は、亀裂、割れが見
られるもの○: No warpage, deformation, cracks, or cracks in resin parts ×: Significant warpage, deformation, or cracks, cracks in resin parts
【0024】[0024]
【表1】 [Table 1]
【0025】[0025]
【発明の効果】本発明のポリアセタール樹脂は、優れた
機械的強度、耐熱性、摺動性を有するだけでなく、成形
時の収縮、後加熱による収縮が小さく優れた寸法安定性
を示すので、精密で寸法安定性を要求されるアウトサー
ト成形の部品等の用途に用いられる。さらに、このポリ
アセタール樹脂を用いる事により、アウトサート部品と
樹脂部品の固着に優れ、樹脂部品のガタツキがなく樹脂
部品の亀裂や割れが極めて少ないアウトサート成形品が
得られる。The polyacetal resin of the present invention not only has excellent mechanical strength, heat resistance, and slidability, but also exhibits excellent dimensional stability with little shrinkage during molding and shrinkage due to post-heating. It is used for parts such as outsert molding parts that require precision and dimensional stability. Further, by using this polyacetal resin, it is possible to obtain an outsert molded product which is excellent in fixing the outsert component and the resin component, has no rattling of the resin component, and has very few cracks or cracks of the resin component.
【図1】 実施例で作製したアウトサート成形品の概略
図である。FIG. 1 is a schematic view of an outsert molded product manufactured in an example.
1 硬質基板(金属部品) 2 ポリアセタール共重合樹脂 3 ランナー部 1 Hard substrate (metal part) 2 Polyacetal copolymer resin 3 Runner part
Claims (4)
のあいた基板に結晶化時間が5分以上のポリアセタール
共重合樹脂の機能部をアウトサート成形法により形成し
たアウトサート成形品。1. An outsert molded article obtained by forming a functional part of a polyacetal copolymer resin having a crystallization time of 5 minutes or more by an outsert molding method on a substrate having at least one notch or hole.
共重合樹脂が、オキシメチレンユニットを主たる構成単
位とする重合体中に炭素数2以上のオキシアルキレンユ
ニットを3〜30重量%含有するものである請求項1記載
のアウトサート成形品。2. A polyacetal copolymer resin having a crystallization time of 5 minutes or more containing 3 to 30% by weight of an oxyalkylene unit having 2 or more carbon atoms in a polymer having an oxymethylene unit as a main constituent unit. The outsert molded article according to claim 1.
トを構成するモノマー成分が、エチレンオキシド、1,3
−ジオキソラン、ジエチレングリコールホルマール、1,
3 −プロパンジオールホルマール、1,4 −ブタンジオー
ルホルマール、1,5 −ペンタンジオールホルマール及び
1,6 −ヘキサンジオールホルマールの何れか1種以上で
ある請求項2記載のアウトサート成形品。3. The monomer component constituting the oxyalkylene unit having 2 or more carbon atoms is ethylene oxide, 1,3
-Dioxolane, diethylene glycol formal, 1,
3-propanediol formal, 1,4-butanediol formal, 1,5-pentanediol formal and
The outsert molded article according to claim 2, which is any one or more of 1,6-hexanediol formal.
デックスが 1.0〜60g/10分である請求項1〜3の何れ
か1項記載のアウトサート成形品。4. The outsert molded article according to claim 1, wherein the polyacetal copolymer resin has a melt index of 1.0 to 60 g / 10 minutes.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27554993A JPH07124997A (en) | 1993-11-04 | 1993-11-04 | Outsert molded article |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27554993A JPH07124997A (en) | 1993-11-04 | 1993-11-04 | Outsert molded article |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH07124997A true JPH07124997A (en) | 1995-05-16 |
Family
ID=17557002
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27554993A Pending JPH07124997A (en) | 1993-11-04 | 1993-11-04 | Outsert molded article |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH07124997A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5952410A (en) * | 1995-09-06 | 1999-09-14 | Asahi Kasei Kogyo Kabushiki Kaisha | Polyacetal resin composition exhibiting high retentivity of mechanical strengths |
US6618241B2 (en) | 2000-11-17 | 2003-09-09 | Samsung Electronics Co., Ltd. | Computer system |
CN111572070A (en) * | 2020-05-22 | 2020-08-25 | 青岛开疆拓土农业装备科技有限公司 | Sealing mechanism of automatic intelligent greenhouse film repairing device |
-
1993
- 1993-11-04 JP JP27554993A patent/JPH07124997A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5952410A (en) * | 1995-09-06 | 1999-09-14 | Asahi Kasei Kogyo Kabushiki Kaisha | Polyacetal resin composition exhibiting high retentivity of mechanical strengths |
US6618241B2 (en) | 2000-11-17 | 2003-09-09 | Samsung Electronics Co., Ltd. | Computer system |
CN111572070A (en) * | 2020-05-22 | 2020-08-25 | 青岛开疆拓土农业装备科技有限公司 | Sealing mechanism of automatic intelligent greenhouse film repairing device |
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