JPH11138642A - Resin frame assembly and assembling method thereof - Google Patents

Resin frame assembly and assembling method thereof

Info

Publication number
JPH11138642A
JPH11138642A JP9310294A JP31029497A JPH11138642A JP H11138642 A JPH11138642 A JP H11138642A JP 9310294 A JP9310294 A JP 9310294A JP 31029497 A JP31029497 A JP 31029497A JP H11138642 A JPH11138642 A JP H11138642A
Authority
JP
Japan
Prior art keywords
resin
resin frame
thermoplastic
resin composition
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.)
Granted
Application number
JP9310294A
Other languages
Japanese (ja)
Other versions
JP3916309B2 (en
Inventor
Kiyoshi Yamamoto
清志 山本
Koichi Shimizu
晃一 清水
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Denka Co Ltd
Original Assignee
Denki Kagaku Kogyo KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Denki Kagaku Kogyo KK filed Critical Denki Kagaku Kogyo KK
Priority to JP31029497A priority Critical patent/JP3916309B2/en
Publication of JPH11138642A publication Critical patent/JPH11138642A/en
Application granted granted Critical
Publication of JP3916309B2 publication Critical patent/JP3916309B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/40General aspects of joining substantially flat articles, e.g. plates, sheets or web-like materials; Making flat seams in tubular or hollow articles; Joining single elements to substantially flat surfaces
    • B29C66/41Joining substantially flat articles ; Making flat seams in tubular or hollow articles
    • B29C66/43Joining a relatively small portion of the surface of said articles
    • B29C66/432Joining a relatively small portion of the surface of said articles for making tubular articles or closed loops, e.g. by joining several sheets ; for making hollow articles or hollow preforms
    • B29C66/4322Joining a relatively small portion of the surface of said articles for making tubular articles or closed loops, e.g. by joining several sheets ; for making hollow articles or hollow preforms by joining a single sheet to itself
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/01General aspects dealing with the joint area or with the area to be joined
    • B29C66/05Particular design of joint configurations
    • B29C66/10Particular design of joint configurations particular design of the joint cross-sections
    • B29C66/11Joint cross-sections comprising a single joint-segment, i.e. one of the parts to be joined comprising a single joint-segment in the joint cross-section
    • B29C66/112Single lapped joints
    • B29C66/1122Single lap to lap joints, i.e. overlap joints
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/40General aspects of joining substantially flat articles, e.g. plates, sheets or web-like materials; Making flat seams in tubular or hollow articles; Joining single elements to substantially flat surfaces
    • B29C66/41Joining substantially flat articles ; Making flat seams in tubular or hollow articles
    • B29C66/43Joining a relatively small portion of the surface of said articles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/70General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
    • B29C66/71General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the composition of the plastics material of the parts to be joined
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/40General aspects of joining substantially flat articles, e.g. plates, sheets or web-like materials; Making flat seams in tubular or hollow articles; Joining single elements to substantially flat surfaces
    • B29C66/49Internally supporting the, e.g. tubular, article during joining

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Injection Moulding Of Plastics Or The Like (AREA)
  • Lining Or Joining Of Plastics Or The Like (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a resin frame assembly that can be used under strict environments having no breakage and deformation due to impact such as dropping or the like or cold heat cycle. SOLUTION: A thermoplastic resin composition is used which consists of a 3-30 wt.% graft polymer obtained by graft-copolymerizing one or more vinyl monomers selected from the group consisting of an aromatic vinyl monomer, a vinyl monomer cyanide, and a methacryl acid ester to 20-87 wt.% polycarbonate resin (A), 10-60 wt.% thermoplastic polyester resin (B), and a rubber polymer (C) for obtaining a molded item having the resin frame and functional part of a molded item with a thermoplastic resin composition, and further a resin frame assembly is made by a method of joining the resin frame and resin part of the molded item through insert molding by a heat welding method.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、落下等の衝撃や冷
熱サイクルによって破損・変形することが無く、厳しい
環境下でも破損・変形することなく使用できる樹脂フレ
ーム組立品およびその組立方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resin frame assembly which can be used without being damaged or deformed by an impact such as a drop or a thermal cycle and can be used without being damaged or deformed even in a severe environment, and a method of assembling the same.

【0002】[0002]

【従来の技術】フレームは組立品における骨格であり、
製品形状の保持を主目的とした部品である。組立品にお
いてはフレームを中心にその他各種の機能部品が接合さ
れており、組立後の使用環境下において様々な性能を維
持できるように設計されている。したがってフレームに
は各種機能部品を確実に固定した状態で十分な強度、剛
性、耐熱性等が要求されるため、安全性の高さから金属
材料が使用されることが多い。
2. Description of the Related Art A frame is a skeleton in an assembly,
This is a part whose main purpose is to maintain the product shape. In the assembled product, various other functional components are joined together around a frame, and are designed so that various performances can be maintained in a use environment after the assembly. Therefore, the frame is required to have sufficient strength, rigidity, heat resistance, etc. in a state in which various functional components are securely fixed, and therefore a metal material is often used from the viewpoint of high safety.

【0003】一方、電気、電子、OA機器用途において
は製品の軽量化要請が強いため、金属よりも比重の小さ
い樹脂フレームの開発が盛んに行われている。特に熱可
塑性樹脂は射出成形、押出成形等の溶融成形加工法が適
用できるため、比較的複雑な形状を有するフレームでも
容易に量産できるメリットがある。フレーム単独はもち
ろんフレームと筐体の一体成形等、組立工数および組立
部品数低減のための様々な検討がなされている。特に発
熱性機能部品を組付けたり、寒冷地で使用されたり、輸
送用車両に搭載したりする場合には、樹脂フレームの耐
熱性、低温強度、耐疲労性での性能不足を補うために、
エンジニアリング樹脂、ポリマーアロイ、フィラー強化
樹脂等の高性能樹脂が使用される。とりわけ要求物性や
コストに応じて比較的自由に樹脂性能を設計できるポリ
マーアロイは特に有効である。
On the other hand, in electric, electronic and OA equipment applications, there is a strong demand for lighter products, and therefore, resin frames having a specific gravity smaller than that of metal have been actively developed. In particular, since a thermoplastic resin can be applied to a melt molding method such as injection molding or extrusion molding, there is an advantage that a frame having a relatively complicated shape can be easily mass-produced. Various studies have been made to reduce the number of assembling steps and the number of assembling parts, such as integral molding of the frame and the housing, as well as the frame alone. Especially when assembling heat-generating functional parts, used in cold regions, or mounted on transportation vehicles, in order to compensate for the lack of performance in heat resistance, low-temperature strength, fatigue resistance of the resin frame,
High performance resins such as engineering resins, polymer alloys, and filler reinforced resins are used. In particular, a polymer alloy that can relatively freely design resin performance according to required physical properties and cost is particularly effective.

【0004】組立工程においては各機能部品をフレーム
に接合する必要があり、ネジ締め、カシメ、接着剤、溶
接等の接合方法がとられている。しかしフレームが樹脂
の場合、ネジ締め、カシメの様に点で接合する方法で接
合すると、局所的に応力が集中してフレームが割れやす
くなる。これを避けるために接合点数を増やす方法も考
えられるが、組立工数や接合用部品点数の増大につなが
るため得策とはいえない。さらに製品の小型化やデザイ
ン形状の多様化により接合部に空間的制約が生じ、ネジ
締めやカシメができない場合も多い。
[0004] In the assembling process, it is necessary to join each functional component to the frame, and joining methods such as screwing, caulking, adhesives, welding, and the like are employed. However, when the frame is made of resin, if the joint is made by a point joining method such as screwing or caulking, stress is locally concentrated and the frame is easily broken. In order to avoid this, a method of increasing the number of joining points is conceivable, but this is not a good measure because it leads to an increase in the number of assembly steps and the number of joining parts. In addition, miniaturization of products and diversification of design shapes cause spatial restrictions at joints, and in many cases, screw tightening and caulking cannot be performed.

【0005】これに対して接着剤および溶接の場合は面
で接合できるために接合部の応力集中は緩和できるが、
別の問題を含有する。溶接の場合は各機能部品が必ずし
も樹脂フレームと同じ材質ではないので、機能部品側に
何らかの細工をしない限り樹脂フレームと直接接合する
のは困難である。また、接着剤は異種の材料同士であっ
ても接合できるため状況に応じて様々な用途で利用され
ているが、接着剤による樹脂のクラック誘発、接着工程
での取扱いの煩雑さ、乾燥工程を必要とすること、廃棄
時の困難な解体性による機能部品の回収しにくさ等の問
題点がある。以上のように、フレームが樹脂である場合
には機能部品との接合において何らかの問題を抱えるこ
とになる。
[0005] On the other hand, in the case of adhesive and welding, since the joints can be made on the surface, the stress concentration at the joint can be alleviated.
Contains another problem. In the case of welding, since each functional component is not necessarily made of the same material as the resin frame, it is difficult to directly join the resin frame without some work on the functional component side. In addition, adhesives are used in various applications depending on the situation because different types of materials can be joined together.However, the adhesive causes cracks in the resin, the handling in the bonding process is complicated, and the drying process is difficult. There is a problem that it is necessary, and it is difficult to collect functional components due to difficult disassembly at the time of disposal. As described above, when the frame is made of resin, there is some problem in joining with the functional component.

【0006】そこで熱可塑性樹脂の特性を生かし、フレ
ーム成形時にインサート成形法を適用し、樹脂が各機能
部品を包みこむ形でフレームごと一気に組立品を完成す
る方法が考えられる。これにより組立工程における接合
が不要になるため、樹脂フレーム組立法としては理想的
といえる。
[0006] Therefore, there is a method in which an insert molding method is applied at the time of frame molding by utilizing the characteristics of the thermoplastic resin, and the resin is wrapped around each functional component to complete the assembly together with the frame at once. This eliminates the need for joining in the assembling process, and is therefore ideal for a resin frame assembling method.

【0007】しかしインサートする各機能部品の材質が
金属やセラミクスである場合、組立後に新たな問題が生
じる。一つは樹脂とインサートする機能部品の密着性の
問題である。密着性が悪いと落下等の衝撃により容易に
ズレが生じる。対策としては、特開平4−169214
号公報において熱可塑性ポリエステル樹脂、ポリカーボ
ネート樹脂、繊維状充填材等を配合した樹脂材料を用い
たインサート成形体が提案されているように、金属やセ
ラミクスとの密着性に優れる樹脂を使用することであ
る。もう一つは金属やセラミクスに比較すると樹脂の線
膨張率は著しく大きく、成形後樹脂の収縮により機能部
品周囲の樹脂に引張応力が発生し、割れが発生しやすく
なる。これらの対策としては、まず機能部品を取り巻く
樹脂の肉厚を十分にとり、熱的な収縮差により発生する
引張応力に耐えられる設計にする方法と、熱可塑性樹脂
に金属または無機の繊維状フィラーを練り込み、樹脂の
線膨張率を低下させる方法がある。
However, when the material of each functional component to be inserted is metal or ceramics, a new problem occurs after assembly. One is the problem of adhesion between the resin and the functional component to be inserted. If the adhesion is poor, misalignment easily occurs due to impact such as dropping. As a countermeasure, Japanese Patent Application Laid-Open No. 4-169214
As disclosed in Japanese Unexamined Patent Publication (Kokai) No. H11-260, an insert molded body using a resin material blended with a thermoplastic polyester resin, a polycarbonate resin, a fibrous filler, or the like is proposed, by using a resin having excellent adhesion to metals and ceramics. is there. The other is that the linear expansion coefficient of the resin is remarkably large as compared with metals and ceramics, and after the resin is shrunk after molding, a tensile stress is generated in the resin around the functional component and cracks are easily generated. As a countermeasure against these problems, first, the thickness of the resin surrounding the functional component should be sufficient, and the design should be such that it can withstand the tensile stress generated by the difference in thermal shrinkage, and a metal or inorganic fibrous filler should be added to the thermoplastic resin. There is a method of mixing and lowering the linear expansion coefficient of the resin.

【0008】以上のような対策を講じることで、製品設
計いかんによっては樹脂フレーム組立にインサート成形
法を適用し、一度の成形工程ですべての機能部品を樹脂
フレームに組みつけて一気に組立品を完成することも可
能と思われる。しかし現実には完成品形状や各機能部品
のレイアウト等、立体的な制約があるため、汎用性のあ
る組立方法とはいい難い。
[0008] By taking the above measures, depending on the product design, the insert molding method is applied to the assembly of the resin frame, and all the functional parts are assembled to the resin frame in a single molding process to complete the assembly at a stretch. It seems possible to do so. However, in reality, there are three-dimensional restrictions such as the shape of the finished product and the layout of each functional component.

【0009】[0009]

【発明が解決しようとする課題】そこで組立品をインサ
ート成形可能な単位まで分割することを考える。すなわ
ち各機能部品を1つまたは複数ずつにグループ分けを
し、各々の機能部品または機能部品グループに対してイ
ンサート成形を行う。そして次の段階でインサートした
成形体の樹脂部分と樹脂フレームを接合し、組立品を完
成するという方法である。この場合は機能部品と樹脂フ
レームのような異種材料を接合する場合と異なり、樹脂
フレーム同士の接合を考えればよいので熱溶接法が適用
できる。したがって熱溶接法により接合することで、点
での接合による応力集中や接着剤使用による取扱い上の
煩雑さ等の問題を回避することができると考えられる。
Therefore, it is considered to divide the assembly into units that can be insert-molded. That is, each functional component is grouped into one or more groups, and insert molding is performed for each functional component or functional component group. Then, in the next step, the resin part of the molded body inserted into the molded body and the resin frame are joined to complete an assembly. In this case, unlike the case of joining different materials such as a functional component and a resin frame, the heat welding method can be applied because the joining of the resin frames may be considered. Therefore, it is considered that joining by the heat welding method can avoid problems such as stress concentration due to joining at a point and complicated handling due to use of an adhesive.

【0010】また、樹脂フレームは材質の剛性不足を補
うために肉厚にしたり、リブを有する形状をとったり、
繊維状フィラーを練り混んだりすることが行われる。こ
のような形状および材質のフレームを熱溶接法により接
合する場合、外部熱源からの熱伝導により接合する方法
では接合面の中心まで均一に加熱できず、十分な接合強
度が得られないため不適当である。そこで、接合面の材
料自身が発熱し、均一に加熱接合する方法が有効であ
る。しかし、以上のように接合強度の向上が図られても
樹脂フレームが破損する部位は接合部であることが多
く、接合部は本質的に強度が低い。仮に接合断面を均一
に溶接できたとしても、接合部はウエルド、ノッチのよ
うないわゆる欠陥部と考えるべきである。より高い耐熱
性の熱可塑性樹脂を使用したり、多量のフィラーを練り
混んだりした場合には接合部位の強度低下がますます目
立つことになる。
The resin frame may be made thick to compensate for the lack of rigidity of the material, or may have a shape having ribs.
Kneading and mixing the fibrous filler are performed. When joining frames of such shape and material by heat welding, the method of joining by heat conduction from an external heat source cannot be heated uniformly to the center of the joining surface, and it is not appropriate because sufficient joining strength cannot be obtained It is. Therefore, it is effective to use a method in which the material of the joining surface itself generates heat and is uniformly heated and joined. However, even if the joint strength is improved as described above, the portion where the resin frame is damaged is often the joint, and the joint has essentially low strength. Even if the joint cross section can be uniformly welded, the joint should be considered as a so-called defective portion such as a weld or a notch. When a thermoplastic resin having higher heat resistance is used, or when a large amount of filler is mixed and mixed, the strength of the joint portion decreases more and more conspicuously.

【0011】[0011]

【課題を解決するための手段】上記の問題点をふまえ、
ポリカーボネート樹脂、熱可塑性ポリエステル樹脂、お
よび特定のグラフト共重合体から成る熱可塑性樹脂組成
物を樹脂フレームとして使用し、機能部品をインサート
成形した後の樹脂のインサート成形体の樹脂部分を樹脂
フレームに熱溶接法で接合したところ、従来の樹脂材料
において破壊しやすい接合部の強度が著しく改良されて
いることがわかり、本発明に至った。すなわち本発明
は、(A)ポリカーボネート樹脂20〜87重量%、
(B)熱可塑性ポリエステル樹脂10〜60重量%、お
よび(C)ゴム状重合体に、芳香族ビニル単量体、シア
ン化ビニル単量体、メタクリル酸エステルよりなる群か
ら選ばれたビニル系単量体の1種類以上をグラフト共重
合したグラフト共重合体3〜30重量%からなる熱可塑
性樹脂組成物を用いて、該熱可塑性樹脂組成物による成
形体の樹脂フレーム、および組立品を構成する機能部品
をインサート成形した成形体を得、更に樹脂フレームと
インサート成形した成形体の樹脂部分を熱溶接法によっ
て接合した樹脂フレーム組立品である。
In view of the above problems,
A thermoplastic resin composition comprising a polycarbonate resin, a thermoplastic polyester resin, and a specific graft copolymer is used as a resin frame, and the resin part of the resin insert molded body after the functional component is insert molded is heated to the resin frame. When welding was performed, it was found that the strength of the joint that was easily broken in the conventional resin material was significantly improved, and the present invention was reached. That is, the present invention provides (A) a polycarbonate resin of 20 to 87% by weight,
(B) 10 to 60% by weight of a thermoplastic polyester resin, and (C) a rubber-like polymer, a vinyl-based monomer selected from the group consisting of an aromatic vinyl monomer, a vinyl cyanide monomer, and a methacrylate ester. Using a thermoplastic resin composition comprising 3 to 30% by weight of a graft copolymer obtained by graft copolymerizing at least one kind of a monomer, a resin frame of a molded article made of the thermoplastic resin composition and an assembly are formed. This is a resin frame assembly in which a molded article obtained by insert-molding a functional component is obtained, and a resin frame and a resin portion of the insert-molded molded article are joined by a heat welding method.

【0012】以下、本発明の熱可塑性樹脂組成物につい
て詳しく説明する。本発明の樹脂フレーム材を構成する
(A)ポリカーボネート樹脂とは、芳香族ヒドロキシ化
合物を原料とし、ホスゲン法またはエステル交換法によ
って得られる重合体または共重合体であれば特に限定は
しない。上記の芳香族ヒドロキシ化合物としては、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、2,2−ビス(4−ヒ
ドロキシフェニル)プロパン、2,2−ビス(4−ヒド
ロキシフェニル)ブタン、2,2−ビス(4−ヒドロキ
シフェニル)オクタン、ビス(4−ヒドロキシフェニ
ル)フェニルメタン、2,2−ビス(4−ヒドロキシ−
3−メチルフェニル)プロパン、1,1−ビス(4−ヒ
ドロキシ−3−t−ブチルフェニル)プロパンのような
ビス(ヒドロキシアリール)アルカン類、1,1−ビス
(4−ヒドロキシフェニル)シクロペンタン、1,1−
ビス(4−ヒドロキシフェニル)シクロヘキサンのよう
なビス(ヒドロキシアリール)シクロアルカン類、4,
4’−ジヒドロキシジフェニルエーテル、4,4’−ジ
ヒドロキシ−3,3’−ジメチルジフェニルエーテルの
ようなジヒドロキシジアリールエーテル類、4,4’−
ジヒドロキシジフェニルスルフィド、4,4’−ジヒド
ロキシ−3,3’−ジメチルジフェニルスルフィドのよ
うなジヒドロキシジアリールスルフィド類、4,4’−
ジヒドロキシジフェニルスルホキシド、4,4’−ジヒ
ドロキシ−3,3’−ジメチルジフェニルスルホキシド
のようなジヒドロキシジアリールスルホキシド類、4,
4’−ジヒドロキシジフェニルスルホン、4,4’−ジ
ヒドロキシ−3,3’−ジメチルジフェニルスルホンの
ようなジヒドロキシジアリールスルホン類等が挙げられ
る。これらは単独でまたは2種類以上混合して使用され
るが、これらの他にピペラジン、ジピペリジル、ハイド
ロキノン、レゾルシン、4,4’−ジヒドロキシジフェ
ニル等を混合して使用しても良い。これらを原料とした
ポリカーボネート樹脂の中では、2,2−ビス(4−ヒ
ドロキシフェニル)−プロパン(ビスフェノールA型)
ポリカーボネートが特に好ましい。
Hereinafter, the thermoplastic resin composition of the present invention will be described in detail. The (A) polycarbonate resin constituting the resin frame material of the present invention is not particularly limited as long as it is a polymer or a copolymer obtained by a phosgene method or a transesterification method using an aromatic hydroxy compound as a raw material. As the aromatic hydroxy compound, bis (4-hydroxyphenyl) methane, 1,1-bis (4
-Hydroxyphenyl) ethane, 2,2-bis (4-hydroxyphenyl) propane, 2,2-bis (4-hydroxyphenyl) butane, 2,2-bis (4-hydroxyphenyl) octane, bis (4-hydroxy Phenyl) phenylmethane, 2,2-bis (4-hydroxy-
Bis (hydroxyaryl) alkanes such as 3-methylphenyl) propane, 1,1-bis (4-hydroxy-3-t-butylphenyl) propane, 1,1-bis (4-hydroxyphenyl) cyclopentane, 1,1-
Bis (hydroxyaryl) cycloalkanes such as bis (4-hydroxyphenyl) cyclohexane, 4,
Dihydroxydiaryl ethers such as 4'-dihydroxydiphenyl ether and 4,4'-dihydroxy-3,3'-dimethyldiphenyl ether;
Dihydroxydiaryl sulfides such as dihydroxydiphenyl sulfide and 4,4'-dihydroxy-3,3'-dimethyldiphenyl sulfide; 4,4'-
Dihydroxydiarylsulfoxides such as dihydroxydiphenylsulfoxide and 4,4′-dihydroxy-3,3′-dimethyldiphenylsulfoxide;
And dihydroxydiarylsulfones such as 4'-dihydroxydiphenylsulfone and 4,4'-dihydroxy-3,3'-dimethyldiphenylsulfone. These may be used alone or as a mixture of two or more types. In addition, piperazine, dipiperidyl, hydroquinone, resorcin, 4,4′-dihydroxydiphenyl, and the like may be used in combination. Among the polycarbonate resins using these as raw materials, 2,2-bis (4-hydroxyphenyl) -propane (bisphenol A type)
Polycarbonates are particularly preferred.

【0013】ポリカーボネート樹脂の粘度平均分子量
は、衝撃強度の点から15,000以上であることが必
要である。一方粘度平均分子量が30,000を越える
と溶融粘度が高くなるため射出成形しにくくなる。した
がって、本発明に用いるポリカーボネート樹脂の粘度平
均分子量は18,000〜28,000の範囲が好適で
ある。
The viscosity average molecular weight of the polycarbonate resin must be 15,000 or more from the viewpoint of impact strength. On the other hand, if the viscosity average molecular weight exceeds 30,000, the melt viscosity becomes high, so that injection molding becomes difficult. Therefore, the viscosity average molecular weight of the polycarbonate resin used in the present invention is preferably in the range of 18,000 to 28,000.

【0014】本発明で使用できる(B)熱可塑性ポリエ
ステル樹脂は、アルキレンテレフタレート繰り返し単位
を主成分とするものであれば特に制限はない。アルキレ
ンテレフタレート繰り返し単位としては、エチレンテレ
フタレート、テトラメチレンテレフタレート、1,4−
シクロヘキシレンテレフタレート等が挙げられ、共重合
可能な成分としてはイソフタル酸等のジカルボン酸や
1,3−プロパンジオール等のジオールが挙げられる。
具体的にはポリエチレンテレフタレート、ポリブチレン
テレフタレート、ポリ1,4−シクロヘキシレンテレフ
タレートであり、特にポリエチレンテレフタレートまた
はポリブチレンテレフタレートが好ましい。
The thermoplastic polyester resin (B) that can be used in the present invention is not particularly limited as long as it contains an alkylene terephthalate repeating unit as a main component. As the alkylene terephthalate repeating unit, ethylene terephthalate, tetramethylene terephthalate, 1,4-
Cyclohexylene terephthalate and the like can be mentioned, and copolymerizable components include dicarboxylic acids such as isophthalic acid and diols such as 1,3-propanediol.
Specific examples include polyethylene terephthalate, polybutylene terephthalate, and poly-1,4-cyclohexylene terephthalate, and polyethylene terephthalate or polybutylene terephthalate is particularly preferred.

【0015】ポリエチレンテレフタレートまたはポリブ
チレンテレフタレートの固有粘度はフェノール/テトラ
クロロエタン=6/4(重量比)を溶媒として温度30
℃で測定した値が0.5〜1.5(dl/g)の範囲の
ものが用いられ、ポリエチレンテレフタレートの場合は
0.6〜1.1(dl/g)、ポリブチレンテレフタレ
ートの場合は0.8〜1.4(dl/g)の範囲が特に
好ましい。
The intrinsic viscosity of polyethylene terephthalate or polybutylene terephthalate is determined by using phenol / tetrachloroethane = 6/4 (weight ratio) as a solvent at a temperature of 30.
A value measured at a temperature in the range of 0.5 to 1.5 (dl / g) is used. In the case of polyethylene terephthalate, it is 0.6 to 1.1 (dl / g). In the case of polybutylene terephthalate, The range of 0.8 to 1.4 (dl / g) is particularly preferred.

【0016】本発明で使用できる(C)グラフト共重合
体は、ゴム状重合体に、芳香族ビニル単量体、シアン化
ビニル単量体、メタクリル酸エステルよりなる群から選
ばれたビニル系単量体の1種類以上をグラフト共重合し
たグラフト共重合体である。ゴム状重合体としては、ブ
タジエン重合体、ブタジエンとこれと共重合可能なビニ
ル単量体との共重合体、アクリル酸−N−ブチルとアク
リル酸エチルとの共重合体、アクリル酸−N−ブチルと
アクリロニトリルとの共重合体、エチレン、プロピレン
およびジエンとの共重合体、ブタジエンと芳香族ビニル
とのブロック共重合体等が挙げられる。グラフト共重合
体を構成する芳香族ビニル単量体としては、例えばスチ
レン、α−メチルスチレン、ビニルトルエン、t−ブチ
ルスチレン、クロロスチレン等のスチレン単量体および
その置換単量体が挙げられ、特にスチレン、α−メチル
スチレンが好ましい。グラフト共重合体を構成するシア
ン化ビニル単量体としては、例えばアクリロニトリル、
メタクリロニトリル、α−クロロアクリロニトリル等が
挙げられ、特にアクリロニトリルが好ましい。グラフト
共重合体を構成するメタクリル酸エステルとしては、メ
タクリル酸メチル、メタクリル酸エチル等が挙げられ、
特にメタクリル酸メチルが好ましい。
[0016] The graft copolymer (C) which can be used in the present invention is a rubber-like polymer obtained by adding a vinyl-based monomer selected from the group consisting of an aromatic vinyl monomer, a vinyl cyanide monomer and a methacrylate ester. It is a graft copolymer obtained by graft copolymerizing at least one kind of a monomer. Examples of the rubbery polymer include a butadiene polymer, a copolymer of butadiene and a vinyl monomer copolymerizable therewith, a copolymer of -N-butyl acrylate and ethyl acrylate, and a copolymer of acrylic acid -N- Copolymers of butyl and acrylonitrile, copolymers of ethylene, propylene and diene, block copolymers of butadiene and aromatic vinyl and the like can be mentioned. Examples of the aromatic vinyl monomer constituting the graft copolymer include styrene monomers such as styrene, α-methylstyrene, vinyltoluene, t-butylstyrene, and chlorostyrene, and substituted monomers thereof. Particularly, styrene and α-methylstyrene are preferred. Examples of the vinyl cyanide monomer constituting the graft copolymer include, for example, acrylonitrile,
Examples thereof include methacrylonitrile and α-chloroacrylonitrile, and acrylonitrile is particularly preferable. Examples of the methacrylate constituting the graft copolymer include methyl methacrylate and ethyl methacrylate.
Particularly, methyl methacrylate is preferred.

【0017】(C)グラフト共重合体は、芳香族ビニル
単量体0〜70モル%、シアン化ビニル単量体0〜60
モル%およびメタクリル酸エステル0〜100モル%の
単量体混合物20〜70重量部をゴム状重合体30〜8
0重量部に対してグラフト率30〜100%の範囲で共
重合したABSグラフト共重合体、MBSグラフト共重
合体、AESグラフト共重合体、アクリル系グラフト共
重合体等の単独または上記共重合体のうち2種類以上の
混合物でもよく、特にABSまたはMBSグラフト共重
合体が好ましい。なお、本発明のグラフト共重合体は、
ゴム状重合体に単量体をグラフト共重合したものであ
り、未グラフトの重合体を含有していてもよい。
(C) The graft copolymer comprises 0 to 70 mol% of an aromatic vinyl monomer and 0 to 60 mol% of a vinyl cyanide monomer.
20 to 70 parts by weight of a monomer mixture of 0 to 100 mol% of a methacrylic acid ester and 30 to 8
Homogenized ABS copolymers, MBS graft copolymers, AES graft copolymers, acrylic graft copolymers, etc., or the above-mentioned copolymers copolymerized at a graft ratio of 30 to 100% with respect to 0 parts by weight Among them, a mixture of two or more of them may be used, and an ABS or MBS graft copolymer is particularly preferable. Incidentally, the graft copolymer of the present invention,
The rubbery polymer is obtained by graft copolymerization of a monomer, and may contain an ungrafted polymer.

【0018】本発明で用いられる熱可塑性樹脂組成物の
割合は、(A)ポリカーボネート樹脂20〜87重量
%、(B)熱可塑性ポリエステル樹脂10〜60重量
%、および(C)ゴム状重合体に、芳香族ビニル単量
体、シアン化ビニル単量体、メタクリル酸エステルより
なる群から選ばれたビニル系単量体の1種類以上をグラ
フト共重合したグラフト共重合体3〜30重量%が好適
である。
The proportion of the thermoplastic resin composition used in the present invention is (A) 20 to 87% by weight of a polycarbonate resin, (B) 10 to 60% by weight of a thermoplastic polyester resin, and (C) a rubbery polymer. A graft copolymer obtained by graft copolymerizing at least one kind of a vinyl monomer selected from the group consisting of an aromatic vinyl monomer, a vinyl cyanide monomer and a methacrylate ester is preferably 3 to 30% by weight. It is.

【0019】(A)ポリカーボネート樹脂が20重量%
未満では、当該熱可塑性樹脂組成物の十分な耐熱と耐衝
撃強度が得られないため、組立品を使用中に割れや熱変
形が発生しやすくなり、87重量%を越えると成形加工
時の流動性が不足するとともに、組立品においてインサ
ートした機能部品との密着性が不足するため機能部品が
ズレてしまい、最悪の場合はずれてしまう可能性があ
る。 (B)熱可塑性ポリエステル樹脂が10重量%未満で
は、やはり当該熱可塑性樹脂組成物を成形する場合成形
加工時の流動性が不足するとともに、組立品においてイ
ンサートした機能部品との密着性が不足するため機能部
品がズレやすくなり、60重量%を越えると組成物の耐
熱性および耐衝撃強度が不足するため、組立品の使用中
に割れや熱変形が発生しやすくなる。 (C)グラフト共重合体が3重量%未満では、当該熱可
塑性樹脂組成物の十分な耐衝撃強度が得られないため組
立品の使用中に割れが発生しやすくなり、30重量%を
越えると組成物の剛性および耐熱性の不足から組立品が
容易に熱変形してしまう。
(A) 20% by weight of polycarbonate resin
If the amount is less than the above, sufficient heat resistance and impact resistance of the thermoplastic resin composition cannot be obtained, so that cracks and thermal deformation are likely to occur during use of the assembly. In addition to the lack of performance, there is a possibility that the functional component is displaced due to insufficient adhesion with the inserted functional component in the assembly, and in the worst case, the functional component is displaced. (B) When the thermoplastic polyester resin is less than 10% by weight, when the thermoplastic resin composition is molded, the fluidity at the time of molding is insufficient, and the adhesion to the functional component inserted in the assembly is insufficient. Therefore, the functional component tends to shift, and if it exceeds 60% by weight, the heat resistance and impact resistance of the composition are insufficient, so that cracks and thermal deformation easily occur during use of the assembly. If the content of the graft copolymer (C) is less than 3% by weight, sufficient impact resistance of the thermoplastic resin composition cannot be obtained, so that cracks are likely to occur during use of the assembly, and if it exceeds 30% by weight. Due to the lack of rigidity and heat resistance of the composition, the assembly is easily thermally deformed.

【0020】本発明で用いる熱可塑性樹脂組成物は、一
般的な熱可塑性樹脂組成物の製造方法が適用できる。例
えば、各成分をタンブラー、スリーハンズミキサー、ヘ
ンシェルミキサー等のブレンダーで予め混合した後、バ
ンバリーミキサー、ブラベンダー、混練ロール、単軸お
よび2軸押出機等によってペレット化したり、定量フィ
ーダー等を用いて各成分を2軸押出機のメインまたはサ
イドフィード口から供給してペレット化したりする方法
が挙げられる。ペレット化した熱可塑性樹脂組成物は、
一般的な射出成形機等によってインサート成形に用いる
ことができる。また、押出機によるペレット化を省き、
各成分を予備混合した後、直接射出成形機の可塑化工程
で混練し、そのままインサート成形することもできる。
As the thermoplastic resin composition used in the present invention, a general method for producing a thermoplastic resin composition can be applied. For example, after each component is previously mixed in a blender such as a tumbler, a three-hands mixer, and a Henschel mixer, pelletized by a Banbury mixer, a Brabender, a kneading roll, a single-screw and a twin-screw extruder, or by using a quantitative feeder or the like. A method of supplying each component from a main or side feed port of a twin-screw extruder and pelletizing the component is exemplified. The pelletized thermoplastic resin composition,
It can be used for insert molding by a general injection molding machine or the like. Also, pelletization by an extruder is omitted,
After the respective components are preliminarily mixed, they can be directly kneaded in a plasticizing step of an injection molding machine and then directly subjected to insert molding.

【0021】また本発明に用いる熱可塑性樹脂組成物に
は、さらにその目的に応じ充填材、熱安定剤、酸化防止
剤、酸無水物、難燃剤、帯電防止剤、紫外線吸収剤、滑
剤、および着色剤等を添加することも可能である。
The thermoplastic resin composition used in the present invention may further contain a filler, a heat stabilizer, an antioxidant, an acid anhydride, a flame retardant, an antistatic agent, an ultraviolet absorber, a lubricant, It is also possible to add a coloring agent and the like.

【0022】特に充填材の添加は樹脂フレーム自体の剛
性を上げることに加え、熱可塑性樹脂組成物の線膨張率
を低下する目的で使用する場合に有効である。具体的な
充填材としては、ガラス繊維、炭素繊維、炭化ケイ素繊
維、アルミナ繊維、アルミナ−シリカ系繊維等の無機繊
維、アラミド繊維等の有機繊維、ステンレススチール繊
維等の金属繊維、カーボン単結晶、チタン酸カリウム単
結晶等のウイスカ、ガラスフレーク、ガラスビーズ、マ
イカ、タルク、およびベントナイト等を挙げることがで
きる。上記充填材に関しては熱可塑性樹脂組成物との接
着性向上目的のために表面処理や集束処理することがで
きる。
In particular, the addition of a filler is effective in increasing the rigidity of the resin frame itself and when used for the purpose of lowering the coefficient of linear expansion of the thermoplastic resin composition. As specific fillers, glass fiber, carbon fiber, silicon carbide fiber, alumina fiber, inorganic fiber such as alumina-silica fiber, organic fiber such as aramid fiber, metal fiber such as stainless steel fiber, carbon single crystal, Examples include whiskers such as potassium titanate single crystal, glass flakes, glass beads, mica, talc, and bentonite. The filler may be subjected to a surface treatment or a bunching treatment for the purpose of improving the adhesion to the thermoplastic resin composition.

【0023】また熱安定剤の添加は、樹脂フレームを成
形する際に、溶融した熱可塑性樹脂組成物の熱劣化を抑
制するのに有効であり、ヒンダードフェノール系、リン
系等の化合物が使用できる。ヒンダードフェノール系化
合物としては、トリエチレングリコール−ビス[3−
(3−t−ブチル−5−メチル−4−ヒドロキシフェニ
ル)プロピオネート]、1,6−ヘキサンジオール−ビ
ス[3−(3,5−ジ−t−ブチル−4−ヒドロキシフ
ェニル)プロピオネート]、ペンタエリスリチル−テト
ラキス[3−(3,5−ジ−t−ブチル−4−ヒドロキ
シフェニル)プロピオネート]、オクタデシル−3−
(3,5−ジ−t−ブチル−4−ヒドロキシフェニル)
プロピオネート、N,N’ヘキサメチレンビス(3,5
−ジ−t−ブチル−4−ヒドロキシ−ヒドロシンナマミ
ド)、3,5−ジ−t−ブチル−4−ヒドロキシ−ベン
ジルフォスフォネート−ジエチルエステル等が挙げられ
る。
The addition of a heat stabilizer is effective in suppressing the thermal deterioration of the molten thermoplastic resin composition when molding the resin frame, and a compound such as a hindered phenol compound or a phosphorus compound is used. it can. As the hindered phenol compound, triethylene glycol-bis [3-
(3-t-butyl-5-methyl-4-hydroxyphenyl) propionate], 1,6-hexanediol-bis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate], penta Erythrityl-tetrakis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate], octadecyl-3-
(3,5-di-t-butyl-4-hydroxyphenyl)
Propionate, N, N'hexamethylenebis (3,5
-Di-t-butyl-4-hydroxy-hydrocinnamide), 3,5-di-t-butyl-4-hydroxy-benzylphosphonate-diethyl ester and the like.

【0024】リン系化合物としては、フォスファイト系
およびフォスフェイト系有機化合物が好ましく、トリフ
ェニルフォスファイト、トリクレジルホスファイト、ト
リスノニルフェニルホスファイト、トリイソオクチルホ
スファイト、トリイソデシルホスファイト、トリステア
リルホスファイト、トリオレイルホスファイト、ビス
(2,4−ジ−t−ブチルフェニル)ペンタエリスリト
ール−ジ−ホスファイト、ビス(2,6−ジ−t−ブチ
ル−4−メチルフェニル)ペンタエリスリトール−ジ−
ホスファイト等の第3級ホスファイト、ジ−2−エチル
ヘキシルハイドロゼンホスファイト、ジラウリルハイド
ロゼンホスファイト、ジオレイルハイドロゼンホスファ
イト等の第2級ホスファイト、エチルアシッドホスフェ
イト、ブチルアシッドホスフェイト、2−エチルヘキシ
ルアシッドホスフェイト、ラウリルアシッドホスフェイ
ト、ステアリルアシッドホスフェイト、オレイルアシッ
ドホスフェイト、ジ−2−エチルヘキシルホスフェイト
等のアシッドホスフェイト等が挙げられる。
As the phosphorus compound, a phosphite or phosphite organic compound is preferable. Triphenyl phosphite, tricresyl phosphite, trisnonyl phenyl phosphite, triisooctyl phosphite, triisodecyl phosphite, Tristearyl phosphite, trioleyl phosphite, bis (2,4-di-t-butylphenyl) pentaerythritol-di-phosphite, bis (2,6-di-t-butyl-4-methylphenyl) pentaerythritol -Ji-
Tertiary phosphites such as phosphites, secondary phosphites such as di-2-ethylhexyl hydrogen phosphite, dilauryl hydrogen phosphite, dioleyl hydrogen phosphite, ethyl acid phosphate, butyl acid phosphate And acid phosphates such as 2-ethylhexyl acid phosphate, lauryl acid phosphate, stearyl acid phosphate, oleyl acid phosphate, and di-2-ethylhexyl phosphate.

【0025】次に、本発明の樹脂フレーム組立品につい
て説明する。本発明の樹脂フレーム組立品は当該熱可塑
性樹脂組成物を用いて、該熱可塑性樹脂組成物による成
形体の樹脂フレーム、および組立品を構成する機能部品
をインサート成形した成形体を得、更に樹脂フレームと
インサート成形した成形体の樹脂部分を熱溶接法で接合
する方法によって組立てることができる。
Next, the resin frame assembly of the present invention will be described. The resin frame assembly of the present invention uses the thermoplastic resin composition to obtain a resin frame of a molded article made of the thermoplastic resin composition, and a molded article obtained by insert-molding a functional component constituting the assembly, and further comprising a resin. It can be assembled by a method of joining the frame and the resin portion of the molded article obtained by insert molding by a heat welding method.

【0026】本発明におけるインサート成形は、溶融状
態にある樹脂を冷却することによって形状付与する際
に、インサートする機能部品と樹脂を一体化するもので
あれば、成形方法を特に限定するものではない。例え
ば、射出成形において金型のキャビティー内に予めイン
サートする機能部品をセットしておいた状態で溶融樹脂
を金型に射出して作製する方法、押出成形においてはイ
ンサートする機能部品を連続的に被覆する形で作製する
方法等が挙げられる。
In the insert molding in the present invention, the molding method is not particularly limited as long as the functional component to be inserted and the resin are integrated when the resin in a molten state is cooled to be shaped. . For example, in injection molding, a method of making a mold by injecting a molten resin into a mold in a state where a functional component to be inserted is set in advance in a cavity of a mold, and in extrusion molding, continuously inserting a functional component to be inserted. A method of producing in the form of coating may be mentioned.

【0027】また、本発明における組立品を構成する機
能部品は、インサート成形時の溶融樹脂との接触時の温
度上昇によって部品の形状および機能が損なわれない限
りにおいて特に限定するものではないが、金属またはセ
ラミクス材料で構成されているかまたは金属またはセラ
ミクス材料でパッケージングされていることが好まし
い。
The functional component constituting the assembly according to the present invention is not particularly limited as long as the shape and function of the component are not impaired by a rise in temperature upon contact with the molten resin during insert molding. Preferably, it is made of metal or ceramic material or packaged with metal or ceramic material.

【0028】本発明における樹脂フレームとインサート
成形した成形体の樹脂部分を熱溶接する方法は、加熱に
より樹脂フレームおよびインサート成形体の樹脂部を溶
接する方法であれば特に限定するものではないが、材料
自身の発熱による溶接方法が好ましい。具体的には摩擦
溶接法、超音波溶接法、高周波溶接法等が挙げられる。
The method for thermally welding the resin frame and the resin part of the insert-molded article in the present invention is not particularly limited as long as it is a method for welding the resin part of the resin frame and the insert molded article by heating. A welding method using heat generated by the material itself is preferable. Specific examples include a friction welding method, an ultrasonic welding method, and a high-frequency welding method.

【0029】[0029]

【実施例】以下、実施例によって本発明を具体的に説明
するが、本発明は実施例にのみ限定されるものではな
い。なお特別なことわり書きのない場合、添加量につい
て使用した単位は重量%または重量部を意味する。
EXAMPLES The present invention will be described below in detail with reference to examples, but the present invention is not limited to the examples. Unless otherwise specified, the unit used for the added amount means% by weight or part by weight.

【0030】実施例1〜3および比較例1〜6 本発明で使用した熱可塑性樹脂組成物を示す。 (1)熱可塑性樹脂組成物の原料 (A)ポリカーボネート樹脂:市販のビスフェノールA
型ポリカーボネート樹脂「カリバー200−13」[住
友ダウ(株)製](粘度平均分子量21,500)を用
いた。
Examples 1 to 3 and Comparative Examples 1 to 6 The thermoplastic resin compositions used in the present invention are shown. (1) Raw material of thermoplastic resin composition (A) Polycarbonate resin: commercially available bisphenol A
Type polycarbonate resin "Calibur 200-13" (manufactured by Sumitomo Dow) (viscosity average molecular weight 21,500) was used.

【0031】(B)熱可塑性ポリエステル樹脂 (B−1)ポリエチレンテレフタレート樹脂:市販のポ
リエチレンテレフタレート樹脂「NEH−2050」
[ユニチカ(株)製]を用いた。 (B−2)ポリブチレンテレフタレート樹脂:市販のポ
リブチレンテレフタレート樹脂「1200S」[東レ
(株)製]を用いた。
(B) Thermoplastic polyester resin (B-1) Polyethylene terephthalate resin: Commercially available polyethylene terephthalate resin "NEH-2050"
[Unitika Ltd.] was used. (B-2) Polybutylene terephthalate resin: A commercially available polybutylene terephthalate resin "1200S" (manufactured by Toray Industries, Inc.) was used.

【0032】(C)スチレン/アクリロニトリル/ブタ
ジエングラフト共重合体:ポリブタジエンラテックス1
00部(固形分50%、平均粒径0.35μm、ゲル含
有率90%)、ステアリン酸ナトリウム1部、ナトリウ
ムホルムアルデヒドスルホキシレート0.1部、EDT
Aテトラナトリウム塩0.08部、硫酸第一鉄0.00
3部および純水200部を窒素ガスで置換された撹拌機
付き反応缶に仕込んだ。温度65℃に加熱した後、アク
リロニトリル25%およびスチレン75%よりなる単量
体混合物50部、t−ドデシルメルカプタン0.3部、
キュメンハイドロパーオキシド0.2部を4時間で連続
添加し、さらに添加終了後65℃で2時間重合させた。
グラフト率は78%、重合率は97%であった。得られ
たラテックスに酸化防止剤を添加した後、塩化カルシウ
ムで塩析し、水洗、乾燥後得られた白色粉末状の共重合
体を用いた。
(C) Styrene / acrylonitrile / butadiene graft copolymer: polybutadiene latex 1
00 parts (solid content 50%, average particle size 0.35 μm, gel content 90%), sodium stearate 1 part, sodium formaldehyde sulfoxylate 0.1 part, EDT
A tetrasodium salt 0.08 part, ferrous sulfate 0.00
3 parts and 200 parts of pure water were charged into a reactor equipped with a stirrer and purged with nitrogen gas. After heating to a temperature of 65 ° C., 50 parts of a monomer mixture consisting of 25% of acrylonitrile and 75% of styrene, 0.3 part of t-dodecyl mercaptan,
0.2 parts of cumene hydroperoxide was continuously added over 4 hours, and after the addition was completed, polymerization was carried out at 65 ° C. for 2 hours.
The graft ratio was 78%, and the polymerization ratio was 97%. After adding an antioxidant to the obtained latex, salting out with calcium chloride, washing with water and drying, a white powdery copolymer obtained was used.

【0033】(2)熱可塑性樹脂組成物の製造方法 実施例および比較例における熱可塑性樹脂組成物は、表
1および表2に示した原料樹脂を重量部配合比でタンブ
ラーを用いて均一に混合した後、単軸押出機「MS40
−32V」(アイ・ケー・ジー(株)製)を使用し、シ
リンダー温度270℃でペレットを作製した。作製した
ペレットを用いて射出成形機「IS−55EPN」(東
芝機械(株)製)により、シリンダー温度270℃、金
型温度60℃でテストピースを作製し、物性測定用に用
いた。また、このテストピースの一部を樹脂フレーム組
立品のフレーム用として用いた。
(2) Production Method of Thermoplastic Resin Composition The thermoplastic resin compositions in Examples and Comparative Examples were prepared by uniformly mixing the raw material resins shown in Tables 1 and 2 in a mixing ratio of parts by weight using a tumbler. After that, the single screw extruder “MS40
Pellets were produced at a cylinder temperature of 270 ° C. using “−32V” (produced by IKG Co., Ltd.). Using the pellets thus produced, a test piece was produced at a cylinder temperature of 270 ° C. and a mold temperature of 60 ° C. using an injection molding machine “IS-55EPN” (manufactured by Toshiba Machine Co., Ltd.) and used for measuring physical properties. A part of the test piece was used for a frame of a resin frame assembly.

【0034】(3)インサート成形および熱溶接法によ
る組立 上記(2)で作製した熱可塑性樹脂組成物のペレットを
用い、外径50mm×厚さ5mmの金属円盤を機能部品とし
て射出成形機「ネスタール75」(住友重機械工業
(株)製)により、シリンダー温度270℃、金型温度
60℃で樹脂肉厚3mmのインサート成形を行った。成形
体の平面図を図1に、平面図におけるAA’の縦断面図
を図2に示す。成形体には断面形状が一辺1mmの正三角
形である溶接用リブを円周状の樹脂部の中心部に設け
た。
(3) Insert molding and assembly by heat welding method Using a pellet of the thermoplastic resin composition prepared in the above (2), a metal disk having an outer diameter of 50 mm and a thickness of 5 mm is used as a functional component and an injection molding machine "Nestal". 75 "(manufactured by Sumitomo Heavy Industries, Ltd.), insert molding was performed at a cylinder temperature of 270 ° C. and a mold temperature of 60 ° C. with a resin thickness of 3 mm. FIG. 1 is a plan view of the molded body, and FIG. 2 is a longitudinal sectional view of AA ′ in the plan view. The molded body was provided with a welding rib having a regular triangular cross section of 1 mm on a side at the center of the circumferential resin portion.

【0035】作製したインサート成形体2個を組み立て
るために、2個のインサート成形体の中心点が127mm
の間隔になるように同種の熱可塑性樹脂組成物で作製し
た長さ127mm、幅12.7mm、厚さ6.35mmの成形
体を樹脂フレームとして超音波接合により熱溶接し、樹
脂フレーム組立品を作製した。組立品の平面図を図3
に、平面図におけるBB’の縦断面図を図4に示す。こ
の時使用した超音波ウエルダーは、精電舎電子工業
(株)製1201B/P46Aで、圧力2kg/cm2、発振
時間0.6秒、保持時間2秒で溶接を行った。
In order to assemble the two insert moldings, the center point of the two insert moldings is 127 mm.
A 127 mm long, 12.7 mm wide, 6.35 mm thick molded body made of the same type of thermoplastic resin composition is heat-welded by ultrasonic bonding to form a resin frame so that the resin frame assembly is formed at a distance of. Produced. Fig. 3 shows a plan view of the assembled product.
FIG. 4 shows a vertical sectional view of BB ′ in the plan view. The ultrasonic welder used at this time was welded with a pressure of 2 kg / cm 2 , an oscillation time of 0.6 seconds and a holding time of 2 seconds with 1201B / P46A manufactured by Seidensha Electronics Industry Co., Ltd.

【0036】(4)測定および評価 表1および表2における物性の測定方法は次の通りであ
る。 (a)高荷重下での耐熱性:ASTM D−648に従
い、試験応力18.6kgf/cm2 で、長さ127mm、幅1
2.7mm、厚さ6.35mmのテストピースの加熱変形温
度を測定した。 (b)ノッチ部の耐衝撃強度:ASTM D−256に
従い、厚さ6.35mmのテストピースを用い、雰囲気温
度23℃、湿度50%のJIS標準状態でノッチ付きア
イゾット衝撃強度を測定した。
(4) Measurement and Evaluation Methods for measuring physical properties in Tables 1 and 2 are as follows. (A) Heat resistance under high load: According to ASTM D-648, test stress is 18.6 kgf / cm 2 , length 127 mm, width 1
The heating deformation temperature of a 2.7 mm thick 6.35 mm test piece was measured. (B) Impact strength of notch: According to ASTM D-256, a notched Izod impact strength was measured using a test piece having a thickness of 6.35 mm under JIS standard conditions of an ambient temperature of 23 ° C and a humidity of 50%.

【0037】(c)超音波溶接による溶接部強度:引張
試験用JIS1号形状のダンベル支点間の中点におい
て、ダンベル表面上の片側に引張方向と直角に直線状に
溶接用リブを走らせたものを射出成形で作製した。溶接
用リブの断面形状は一辺1mmの正三角形である。続いて
ダンベルを溶接用リブと平行方向にリブから2.5mm離
れた位置において切断した。この切断した二つのダンベ
ルを図5のように配置し、リブをはさむ形で重ね合わせ
部分を作り、そのまま冶具に固定した。重ね合わせ部分
に対してダンベル表面と垂直方向に超音波溶接用ホーン
を当てて圧力をかけながら超音波を発振させてリブを中
心に溶接を行った。この時使用した超音波ウエルダー
は、精電舎電子工業(株)製1201B/P46Aで、
圧力2kg/cm2、発振時間0.6秒、保持時間2秒で溶接
を行った。溶接後のダンベル試験片をASTM D−6
38に従って引張試験を行い、溶接部強度を測定した。
(C) Strength of the welded portion by ultrasonic welding: A welding rib running linearly perpendicular to the pulling direction on one side of the dumbbell surface at the midpoint between JIS No. 1 dumbbell fulcrum points for tensile testing. Was produced by injection molding. The cross-sectional shape of the welding rib is a regular triangle having a side of 1 mm. Subsequently, the dumbbell was cut at a position 2.5 mm away from the rib in a direction parallel to the welding rib. The two cut dumbbells were arranged as shown in FIG. 5, and an overlapped portion was formed by sandwiching a rib, and was fixed to a jig as it was. An ultrasonic welding horn was applied to the overlapped portion in a direction perpendicular to the surface of the dumbbell, and ultrasonic waves were oscillated while applying pressure to perform welding around the ribs. The ultrasonic welder used at this time was 1201B / P46A manufactured by Seidensha Electronics Co., Ltd.
The welding was performed at a pressure of 2 kg / cm 2 , an oscillation time of 0.6 seconds, and a holding time of 2 seconds. ASTM D-6 for dumbbell specimen after welding
A tensile test was performed according to No. 38 to measure the strength of the weld.

【0038】(d)組立品テスト (d−1)落下テスト 上記(2)で作製した熱可塑性樹脂組成物のペレットを
用いて作製した樹脂フレーム組立品をコンクリートの床
に対して1mの高さから自由落下させ、落下時の衝撃に
よる樹脂フレームの破損状況を観察した。また、インサ
ートした機能部品と樹脂の密着性が十分でない場合には
落下時の衝撃よって機能部品が樹脂部分からズレてしま
うことがあるため、部品のズレ状態も合わせて観察し
た。 (d−2)ヒートサイクルテスト 上記(2)で作製した熱可塑性樹脂組成物のペレットを
用いて作製した樹脂フレーム組立品を、環境温度−40
℃と85℃において3時間ずつ冷熱サイクルを5回繰り
返した後、組立品を観察した。
(D) Assembly test (d-1) Drop test The resin frame assembly produced using the pellets of the thermoplastic resin composition produced in the above (2) was 1 m above the concrete floor. From the resin frame, and the state of damage of the resin frame due to the impact at the time of the fall was observed. In addition, if the adhesiveness between the inserted functional component and the resin is not sufficient, the functional component may be displaced from the resin portion due to an impact at the time of dropping. Therefore, the displaced state of the component was also observed. (D-2) Heat cycle test The resin frame assembly produced using the thermoplastic resin composition pellets produced in the above (2) was subjected to an environmental temperature of -40.
The assembly was observed after 5 cycles of cooling and heating at 3 ° C. and 85 ° C. each for 3 hours.

【0039】[0039]

【表1】 [Table 1]

【0040】[0040]

【表2】 [Table 2]

【0041】本発明における組立法で作製された樹脂フ
レームの落下衝撃強度は、組立品の落下テストで評価で
きた。また、実際製品レベルの樹脂フレーム組立品にお
いては所望の剛性やデザインを付与するために樹脂フレ
ームを肉厚にしたり、リブを設けたり複雑な形状をとる
ことがあるので熱可塑性樹脂組成物そのもののノッチ部
の耐衝撃強度も重要となる。したがって、樹脂フレーム
組立品においては組立品落下テスト、溶接部の強度、高
荷重下の耐熱性、ノッチ部の耐衝撃性について総合的な
性能(物性バランス等)が要求されることとなる。
The drop impact strength of the resin frame produced by the assembling method in the present invention could be evaluated by a drop test of the assembled product. In addition, in the actual product level resin frame assembly, the resin frame may be made thicker, provided with ribs or formed in a complicated shape in order to impart a desired rigidity or design. The impact strength of the notch is also important. Therefore, the resin frame assembly is required to have comprehensive performance (such as balance of physical properties) in terms of an assembly drop test, strength of a welded portion, heat resistance under a high load, and impact resistance of a notch portion.

【0042】[0042]

【発明の効果】本発明の熱可塑性樹脂組成物の成形体を
組立品のフレームに用い、熱溶接法により組み立てた樹
脂フレーム組立品は、落下等の衝撃で破損すること無
く、厳しい環境下でも破損・変形することなく使用する
ことができる。
According to the present invention, a molded article of the thermoplastic resin composition of the present invention is used for a frame of an assembly, and a resin frame assembly assembled by a heat welding method is not damaged by a shock such as dropping, and can be used in a severe environment. It can be used without being damaged or deformed.

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明の熱可塑性樹脂組成物を用いたインサー
ト成形体の平面図である。
FIG. 1 is a plan view of an insert molded body using a thermoplastic resin composition of the present invention.

【図2】図1のAA’におけるインサート成形体の縦断
面図である。
FIG. 2 is a longitudinal sectional view of the insert molded body taken along AA ′ of FIG.

【図3】本発明の熱可塑性樹脂組成物を用いた樹脂フレ
ームとインサート成形体2個を超音波溶接により接合し
た樹脂フレーム組立品の平面図である。
FIG. 3 is a plan view of a resin frame assembly obtained by joining a resin frame and two insert molded bodies using the thermoplastic resin composition of the present invention by ultrasonic welding.

【図4】図3のBB’における樹脂フレーム組立品の縦
断面図である。
FIG. 4 is a vertical sectional view of the resin frame assembly taken along BB ′ in FIG. 3;

【図5】超音波溶接強度評価用のJIS1号ダンベルを
超音波溶接するための配置図である。
FIG. 5 is a layout view for ultrasonic welding a JIS No. 1 dumbbell for ultrasonic welding strength evaluation.

【符号の説明】[Explanation of symbols]

1 熱可塑性樹脂組成物 2 インサート金属円盤 3 溶接用リブ(断面形状:一辺1mmの正三角形) 4 溶接部 5 切断した溶接用リブ付きのJIS1号ダンベル DESCRIPTION OF SYMBOLS 1 Thermoplastic resin composition 2 Insert metal disk 3 Welding rib (Cross-sectional shape: equilateral triangle of 1 mm side) 4 Welded part 5 JIS No. 1 dumbbell with cut welding rib

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI C08L 67:02 55:02) B29K 67:00 69:00 105:06 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code FI C08L 67:02 55:02) B29K 67:00 69:00 105: 06

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 (A)ポリカーボネート樹脂20〜87
重量%、(B)熱可塑性ポリエステル樹脂10〜60重
量%、および(C)ゴム状重合体に、芳香族ビニル単量
体、シアン化ビニル単量体、メタクリル酸エステルより
なる群から選ばれたビニル系単量体の1種類以上をグラ
フト共重合したグラフト共重合体3〜30重量%からな
る熱可塑性樹脂組成物を用いて、該熱可塑性樹脂組成物
による成形体の樹脂フレーム、および組立品を構成する
機能部品をインサート成形した成形体を得、さらに樹脂
フレームとインサート成形した成形体の樹脂部分を熱溶
接法で接合する方法によって得ることを特徴とする樹脂
フレーム組立品。
1. A polycarbonate resin 20 to 87
% By weight, (B) 10 to 60% by weight of a thermoplastic polyester resin, and (C) a rubbery polymer selected from the group consisting of an aromatic vinyl monomer, a vinyl cyanide monomer, and a methacrylate ester. Using a thermoplastic resin composition comprising 3 to 30% by weight of a graft copolymer obtained by graft copolymerizing one or more vinyl monomers, a resin frame of a molded article made of the thermoplastic resin composition, and an assembled product A resin frame assembly obtained by obtaining a molded article obtained by insert-molding the functional component constituting the above, and further by joining the resin portion of the molded article obtained by insert molding to the resin frame by a heat welding method.
【請求項2】 請求項1記載の熱可塑性樹脂組成物を用
いて、該熱可塑性樹脂組成物による成形体の樹脂フレー
ム、および組立品を構成する機能部品をインサート成形
した成形体を得、更に樹脂フレームとインサート成形し
た成形体の樹脂部分を熱溶接法で接合する方法によって
組立てることを特徴とする樹脂フレーム組立品の組立方
法。
2. A molded article obtained by insert-molding a resin frame of a molded article made of the thermoplastic resin composition and a functional component constituting an assembly, using the thermoplastic resin composition according to claim 1, further comprising: A method for assembling a resin frame assembly, comprising: assembling a resin frame and a resin portion of a molded article formed by insert molding by a heat welding method.
【請求項3】 (A)ポリカーボネート樹脂が2,2−
ビス(4−ヒドロキシフェニル)−プロパン(ビスフェ
ノールA型)ポリカーボネート、(B)熱可塑性ポリエ
ステル樹脂がポリエチレンテレフタレートおよびポリブ
チレンテレフタレートから選ばれた1種以上、並びに
(C)グラフト共重合体がABSグラフト共重合体から
なる熱可塑性樹脂組成物を用いることを特徴とする請求
項1記載の樹脂フレーム組立品。
3. The method of claim 2, wherein (A) the polycarbonate resin is 2,2-
Bis (4-hydroxyphenyl) -propane (bisphenol A type) polycarbonate; (B) at least one thermoplastic polyester resin selected from polyethylene terephthalate and polybutylene terephthalate; and (C) a graft copolymer comprising an ABS graft copolymer. The resin frame assembly according to claim 1, wherein a thermoplastic resin composition comprising a polymer is used.
JP31029497A 1997-11-12 1997-11-12 Resin frame assembly and assembly method thereof Expired - Fee Related JP3916309B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31029497A JP3916309B2 (en) 1997-11-12 1997-11-12 Resin frame assembly and assembly method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31029497A JP3916309B2 (en) 1997-11-12 1997-11-12 Resin frame assembly and assembly method thereof

Publications (2)

Publication Number Publication Date
JPH11138642A true JPH11138642A (en) 1999-05-25
JP3916309B2 JP3916309B2 (en) 2007-05-16

Family

ID=18003497

Family Applications (1)

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Country Status (1)

Country Link
JP (1) JP3916309B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2003085046A1 (en) * 2002-04-08 2005-08-11 ウィンテックポリマー株式会社 Laser welded polybutylene terephthalate resin composition and molded article
JP2006233437A (en) * 2005-02-22 2006-09-07 Kii Techno Kk Transparent protecting tube for outer cable
JP2015066846A (en) * 2013-09-30 2015-04-13 Dic株式会社 Method for producing structure and method for producing battery lid
EP1624012B2 (en) 2003-05-12 2015-09-02 Teijin Chemicals, Ltd. Sheet-form window member and window structure

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