JPH10315333A - Polyamide resin vibration welding molding - Google Patents

Polyamide resin vibration welding molding

Info

Publication number
JPH10315333A
JPH10315333A JP13192497A JP13192497A JPH10315333A JP H10315333 A JPH10315333 A JP H10315333A JP 13192497 A JP13192497 A JP 13192497A JP 13192497 A JP13192497 A JP 13192497A JP H10315333 A JPH10315333 A JP H10315333A
Authority
JP
Japan
Prior art keywords
resin
vibration
welding
polyamide resin
copolyamide
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
Application number
JP13192497A
Other languages
Japanese (ja)
Inventor
Hiroshi Urabe
宏 浦部
Hajime Oyama
一 大山
Tatsuya Hitomi
達也 人見
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.)
Mitsubishi Engineering Plastics Corp
Original Assignee
Mitsubishi Engineering Plastics Corp
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 Mitsubishi Engineering Plastics Corp filed Critical Mitsubishi Engineering Plastics Corp
Priority to JP13192497A priority Critical patent/JPH10315333A/en
Publication of JPH10315333A publication Critical patent/JPH10315333A/en
Pending 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
    • B29C66/70General 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
    • B29C65/00Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
    • B29C65/02Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure
    • B29C65/06Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure using friction, e.g. spin welding
    • 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
    • B29C66/13Single flanged joints; Fin-type joints; Single hem joints; Edge joints; Interpenetrating fingered joints; Other specific particular designs of joint cross-sections not provided for in groups B29C66/11 - B29C66/12
    • B29C66/131Single flanged joints, i.e. one of the parts to be joined being rigid and flanged in the joint area
    • B29C66/1312Single flange to flange joints, the parts to be joined being rigid
    • 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
    • B29C66/302Particular design of joint configurations the area to be joined comprising melt initiators
    • B29C66/3022Particular design of joint configurations the area to be joined comprising melt initiators said melt initiators being integral with at least one of the parts to be joined
    • B29C66/30223Particular design of joint configurations the area to be joined comprising melt initiators said melt initiators being integral with at least one of the parts to be joined said melt initiators being rib-like
    • 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
    • B29C66/50General aspects of joining tubular articles; General aspects of joining long products, i.e. bars or profiled elements; General aspects of joining single elements to tubular articles, hollow articles or bars; General aspects of joining several hollow-preforms to form hollow or tubular articles
    • B29C66/51Joining tubular articles, profiled elements or bars; Joining single elements to tubular articles, hollow articles or bars; Joining several hollow-preforms to form hollow or tubular articles
    • B29C66/54Joining several hollow-preforms, e.g. half-shells, to form hollow articles, e.g. for making balls, containers; Joining several hollow-preforms, e.g. half-cylinders, to form tubular articles
    • B29C66/547Joining several hollow-preforms, e.g. half-cylinders, to form tubular articles, e.g. endless tubes
    • B29C66/5474Joining several hollow-preforms, e.g. half-cylinders, to form tubular articles, e.g. endless tubes for making fork-shaped pieces, i.e. with 3 branches, e.g. Y-shaped pieces
    • 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
    • B29C66/72General 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 structure of the material of the parts to be joined
    • B29C66/721Fibre-reinforced materials
    • B29C66/7212Fibre-reinforced materials characterised by the composition of the fibres
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29LINDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2031/00Other particular articles
    • B29L2031/24Pipe joints or couplings
    • B29L2031/246T-joints
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29LINDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2031/00Other particular articles
    • B29L2031/748Machines or parts thereof not otherwise provided for
    • B29L2031/749Motors
    • B29L2031/7492Intake manifold

Landscapes

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

Abstract

PROBLEM TO BE SOLVED: To improve strength, heat resistance and welding strength of a welding molding by vibration welding a plurality of moldings molded from polyamide resin composition obtained by mixing specific amount of glass fiber with polyimide resin made of specific amount of homopolyamide resin and copolyamide resin. SOLUTION: This molding is obtained by mixing 10 to 100 pts.wt. of glass fiber with 100 pts.wt. of polyamide resin containing 95 to 50 wt.% of homopolyamide resin and 5 to 50 wt.% of copolyamide resin. First, a plurality of components are molded, for example, by using the composition by an injection molding process. The plurality of the molded moldings are connected by vibration welding to obtain a polyamide resin vibration welded molding. A frequency of the vibration in the welding is 100 to 300 Hz, its amplitude is 0.5 to 2.0 mm, or preferably 0.8 to 1.6 mm. The welding pressure is 5 to 100 kg/cm<2> or preferably 10 to 60 kg/cm<2> .

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、ポリアミド樹脂製
振動溶着成形品に関するものであり、詳しくは、一次成
形した複数の成形品を振動溶着により接合し一体化した
ポリアミド樹脂製振動溶着成形品に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a vibration-welded molded article made of a polyamide resin, and more particularly to a vibration-welded molded article of a polyamide resin obtained by joining a plurality of primary molded articles by vibration welding. Things.

【0002】[0002]

【従来の技術】近年、プラスチックの用途が拡大され、
その特性を生かし、各種工業製品、例えば自動車エンジ
ンのインテークマニホールドなども振動溶着法により樹
脂化が試みられている。樹脂化の材料としてはガラス繊
維強化66ナイロンまたはガラス繊維強化6ナイロンな
どが用いられている。
2. Description of the Related Art In recent years, applications of plastics have been expanded,
Taking advantage of this property, various industrial products, such as intake manifolds for automobile engines, have been converted into resins by the vibration welding method. As a material for resinification, glass fiber reinforced 66 nylon or glass fiber reinforced 6 nylon is used.

【0003】しかし、従来の方法では、一次成形された
成形品を振動溶着法により溶着しても充分に満足できる
溶着強度が得られず、例えば振動溶着成形品が中空体成
形品である自動車エンジンのインテークマニホールドの
場合においては十分な耐圧強度が得られず、エンジンの
バックファイアなどによって内圧が増大したときに破損
する恐れがある。このため、溶着強度を向上する手段と
して、使用するポリアミド樹脂の相対粘度を増大する方
法や溶着面積を増大する方法等が知られているが、前者
においては流動性の低下が生じ、後者においては設計変
更の必要があった。
However, in the conventional method, even if the primary molded article is welded by the vibration welding method, a satisfactory welding strength cannot be obtained. For example, an automobile engine in which the vibration weld molded article is a hollow body molded article In the case of the intake manifold described above, sufficient pressure resistance cannot be obtained, and the intake manifold may be damaged when the internal pressure increases due to backfire of the engine or the like. For this reason, as a means for improving the welding strength, a method of increasing the relative viscosity of the polyamide resin to be used, a method of increasing the welding area, and the like are known, but in the former, a decrease in fluidity occurs, and in the latter, A design change was required.

【0004】[0004]

【発明が解決しようとする課題】本発明の目的は、強
度、耐熱性、耐薬品性に優れ、且つ溶着強度に優れたポ
リアミド樹脂製振動溶着成形品を提供することにある。
SUMMARY OF THE INVENTION An object of the present invention is to provide a vibration-welded molded article made of a polyamide resin which is excellent in strength, heat resistance, chemical resistance and welding strength.

【0005】[0005]

【課題を解決するための手段】本発明は、上述の問題を
解決するためになされたものであり、その要旨は、ホモ
ポリアミド樹脂95〜50重量%とコポリアミド樹脂5
〜50重量%とからなるポリアミド樹脂成分100重量
部に対し、ガラス繊維10〜100重量部を配合してな
るポリアミド樹脂組成物を用いて一次成形した複数の成
形品を振動溶着してなるポリアミド樹脂製振動溶着成形
品に存する。
SUMMARY OF THE INVENTION The present invention has been made to solve the above-mentioned problems, and the gist of the present invention is that a homopolyamide resin of 95 to 50% by weight and a copolyamide resin
Polyamide resin obtained by vibration-welding a plurality of molded products that are primarily molded using a polyamide resin composition obtained by mixing 10 to 100 parts by weight of glass fiber with respect to 100 parts by weight of a polyamide resin component of 50 to 50% by weight. Vibration welding molded products.

【0006】以下、本発明につき詳細に説明する。本発
明におけるホモポリアミド樹脂およびコポリアミド樹脂
における構成単位となる原料としては、重合可能なω−
アミノ酸類もしくはそのラクタム類、好ましくは3員環
以上のラクタム、または二塩基酸類とジアミン類などが
挙げられる。
Hereinafter, the present invention will be described in detail. As a raw material serving as a structural unit in the homopolyamide resin and the copolyamide resin in the present invention, polymerizable ω-
Examples include amino acids or lactams thereof, preferably lactams having three or more ring members, or dibasic acids and diamines.

【0007】ω−アミノ酸類としては、ε−アミノカプ
ロン酸、7−アミノヘプタン酸、9−アミノノナン酸、
11−アミノウンデカン酸、12−アミノドデカン酸が
挙げられる。ラクタム類としては、ε−カプロラクタ
ム、エナントラクタム、カプリルラクタム、ラウリルラ
クタム、α−ピロリドン、α−ピペリドンが挙げられ
る。
The ω-amino acids include ε-aminocaproic acid, 7-aminoheptanoic acid, 9-aminononanoic acid,
Examples thereof include 11-aminoundecanoic acid and 12-aminododecanoic acid. Lactams include ε-caprolactam, enantholactam, caprylactam, lauryl lactam, α-pyrrolidone and α-piperidone.

【0008】二塩基酸類としては、アジピン酸、グルタ
ル酸、ピメリン酸、スベリン酸、アゼライン酸、セバシ
ン酸、ダイマー酸、ウンデカンジオン酸、ドデカジオン
酸、ヘキサデカジオン酸、ヘキサデセンジオン酸、エイ
コサンジオン酸、エイコサジエンジオン酸、ジグリコー
ル酸、2,2,4−トリメチルアジピン酸、キシリレン
ジカルボン酸、1,4−シクロヘキサンジカルボン酸、
テレフタル酸、イソフタル酸が挙げられる。ジアミン類
としては、ヘキサメチレンジアミン、テトラメチレンジ
アミン、ノナメチレンジアミン、ウンデカメチレンジア
ミン、ドデカメチレンジアミン、2,2,4(または
2,4,4)−トリメチルヘキサメチレンジアミン、ビ
ス−(4,4’−アミノシクロヘキシル)メタン、メタ
キシリレンジアミンが挙げられる。
The dibasic acids include adipic acid, glutaric acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, dimer acid, undecandionic acid, dodecadionic acid, hexadecadionic acid, hexadecenedionic acid, eicosandioic acid , Eicosadienedioic acid, diglycolic acid, 2,2,4-trimethyladipic acid, xylylenedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid,
Terephthalic acid and isophthalic acid; Diamines include hexamethylenediamine, tetramethylenediamine, nonamethylenediamine, undecamethylenediamine, dodecamethylenediamine, 2,2,4 (or 2,4,4) -trimethylhexamethylenediamine, bis- (4, 4'-aminocyclohexyl) methane and meta-xylylenediamine.

【0009】本発明におけるホモポリアミド樹脂として
は、6ナイロン、66ナイロン等が挙げられ、好ましく
は6ナイロンが挙げられる。ホモポリアミド樹脂の相対
粘度は、JIS K6810に従って98%硫酸中濃度
1%、温度25℃で測定した値で、好ましくは、2.0
〜4.0である。相対粘度が2.0未満であると溶着強
度が小さくなり、4.0を越えると流動性低下する。ホ
モポリアミド樹脂の相対粘度は、より好ましくは、2.
5〜3.7である。
The homopolyamide resin in the present invention includes 6 nylon, 66 nylon, and the like, preferably 6 nylon. The relative viscosity of the homopolyamide resin is a value measured at a concentration of 1% in 98% sulfuric acid and a temperature of 25 ° C. according to JIS K6810, and is preferably 2.0%.
44.0. If the relative viscosity is less than 2.0, the welding strength will be low, and if it exceeds 4.0, the fluidity will be reduced. The relative viscosity of the homopolyamide resin is more preferably 2.
5 to 3.7.

【0010】本発明におけるコポリアミド樹脂として
は、好ましくは、融点が180℃〜220℃である結晶
性コポリアミド樹脂、または非晶性コポリアミド樹脂が
挙げられる。 コポリアミド樹脂が結晶性コポリアミド
樹脂である場合、融点が180℃未満であると固化速度
が遅くなり、融点が220℃を越えると溶着強度が低下
する。
[0010] The copolyamide resin in the present invention is preferably a crystalline copolyamide resin having a melting point of 180 ° C to 220 ° C or an amorphous copolyamide resin. When the copolyamide resin is a crystalline copolyamide resin, if the melting point is lower than 180 ° C., the solidification rate is reduced, and if the melting point exceeds 220 ° C., the welding strength is reduced.

【0011】本発明におけるコポリアミド樹脂の種類と
しては、好ましくは、6/66ナイロン、6/6Tナイ
ロン、6I/6Tナイロン等が挙げられ、より好ましく
は、融点が180℃〜220℃である6/66ナイロ
ン、融点が180℃〜220℃である6/6Tナイロ
ン、非晶性の6I/6Tナイロン等が挙げられる。コポ
リアミド樹脂としては複数種を使用することもできる。
ここで、6/6Tナイロンは、構成単位がカプロラクタ
ム単位およびテレフタール酸とヘキサメチレンジアミン
とからなるポリアミド形成単位であるコポリアミド樹脂
であり、6I/6Tナイロンは、構成単位がイソフター
ル酸とヘキサメチレンジアミンとからなるポリアミド形
成単位およびテレフタール酸とヘキサメチレンジアミン
とからなるポリアミド形成単位であるコポリアミド樹脂
である。
The type of the copolyamide resin in the present invention is preferably 6/66 nylon, 6 / 6T nylon, 6I / 6T nylon, or the like, and more preferably has a melting point of 180 ° C. to 220 ° C. / 66 nylon, 6 / 6T nylon having a melting point of 180 ° C to 220 ° C, and amorphous 6I / 6T nylon. A plurality of copolyamide resins may be used.
Here, 6 / 6T nylon is a copolyamide resin whose constituent unit is a caprolactam unit and a polyamide-forming unit composed of terephthalic acid and hexamethylenediamine, and 6I / 6T nylon has a constituent unit of isophthalic acid and hexamethylenediamine. And a copolyamide resin which is a polyamide forming unit comprising terephthalic acid and hexamethylenediamine.

【0012】コポリアミド樹脂の相対粘度は、JIS
K6810に従って98%硫酸中濃度1%、温度25℃
で測定した値で、好ましくは、2.0〜4.0である。
相対粘度が2.0未満であると溶着強度が小さくなり、
4.0を越えると流動性低下する。コポリアミド樹脂の
相対粘度は、より好ましくは、2.5〜3.7である。
The relative viscosity of the copolyamide resin is determined according to JIS.
According to K6810 98% sulfuric acid concentration 1%, temperature 25 ° C
It is preferably 2.0 to 4.0.
If the relative viscosity is less than 2.0, the welding strength is reduced,
If it exceeds 4.0, the fluidity will decrease. The relative viscosity of the copolyamide resin is more preferably from 2.5 to 3.7.

【0013】コポリアミド樹脂の配合量は、ホモポリア
ミド樹脂とコポリアミド樹脂とのポリアミド成分の5〜
50重量%である。コポリアミド樹脂の配合量が5重量
%未満であると溶着強度が低下し、50重量%を越える
と固化速度が遅くなる。コポリアミド樹脂の配合量は、
好ましくは、ホモポリアミド樹脂とコポリアミド樹脂と
のポリアミド成分の7〜40重量%であり、より好まし
くは、10〜35重量%である。
The compounding amount of the copolyamide resin is 5 to 5 of the polyamide component of the homopolyamide resin and the copolyamide resin.
50% by weight. If the amount of the copolyamide resin is less than 5% by weight, the welding strength is reduced, and if it exceeds 50% by weight, the solidification rate is reduced. The compounding amount of the copolyamide resin is
Preferably, it is 7 to 40% by weight, more preferably 10 to 35% by weight of the polyamide component of the homopolyamide resin and the copolyamide resin.

【0014】本発明におけるガラス繊維としては、通
常、熱可塑性樹脂に使用されるものでよく、好ましく
は、Eガラス(無アルカリガラス)から作られるチョッ
プドストランドが挙げられる。ガラス繊維の繊維径は1
〜20μmであり、好ましくは5〜15μmである。ガ
ラス繊維としては、ポリアミド樹脂との接着性の向上の
ためにシランカップリング剤などで表面処理されている
ガラス繊維が好ましい。
The glass fibers in the present invention may be those usually used for thermoplastic resins, and preferably include chopped strands made of E glass (alkali-free glass). Fiber diameter of glass fiber is 1
To 20 μm, preferably 5 to 15 μm. As the glass fiber, a glass fiber that has been surface-treated with a silane coupling agent or the like to improve the adhesion to the polyamide resin is preferable.

【0015】ガラス繊維の配合量は、ホモポリアミド樹
脂とコポリアミド樹脂からなるポリアミド樹脂成分10
0重量部に対して、10〜100重量部である。ガラス
繊維の配合量が10重量部未満であると溶着強度が低下
し、100重量部を越えると流動性が低下する。ガラス
繊維の配合量は、ホモポリアミド樹脂とコポリアミド樹
脂からなるポリアミド樹脂成分100重量部に対して、
好ましくは15〜80重量部、さらに好ましくは20〜
70重量部である。
The blending amount of the glass fiber is a polyamide resin component 10 consisting of a homopolyamide resin and a copolyamide resin.
It is 10 to 100 parts by weight with respect to 0 parts by weight. If the amount of the glass fiber is less than 10 parts by weight, the welding strength decreases, and if it exceeds 100 parts by weight, the fluidity decreases. The blending amount of the glass fiber is based on 100 parts by weight of a polyamide resin component composed of a homopolyamide resin and a copolyamide resin.
Preferably 15-80 parts by weight, more preferably 20-80 parts by weight.
70 parts by weight.

【0016】本発明におけるポリアミド樹脂組成物中に
は、本発明の効果を損なわない範囲において、ガラス繊
維以外の無機充填材、例えばガラスフレーク、ガラスビ
ーズ、マイカ、タルク、カオリン、ウォラストナイト、
チタン酸カリウムウィスカー等を配合してもよい。ま
た、銅化合物などの熱安定剤、離型剤、カーボンブラッ
クなどの着色剤等の公知の添加剤を配合してもよい。こ
れらの配合は、樹脂の重合から成形までの任意の段階で
実施されるが、押出機を用いて溶融混練するのが好まし
い。
In the polyamide resin composition of the present invention, inorganic fillers other than glass fibers, such as glass flakes, glass beads, mica, talc, kaolin, wollastonite, and the like, as long as the effects of the present invention are not impaired.
A potassium titanate whisker or the like may be blended. Further, known additives such as a heat stabilizer such as a copper compound, a releasing agent, and a coloring agent such as carbon black may be blended. These blending is carried out at any stage from the polymerization of the resin to the molding, but it is preferable to carry out melt-kneading using an extruder.

【0017】本発明のポリアミド樹脂製振動溶着成形品
は、ポリアミド樹脂組成物を用いて、まず複数の部品を
それぞれ一次成形する。一次成形により得られる成形品
の成形法としては、熱可塑性樹脂の成形において通常用
いられる成形法が適用され、好ましくは射出成形法が挙
げられる。本発明における一次成形により得られる複数
の成形品はお互いに同じ形状であっても異なる形状であ
ってもよく、例えば、図1に示すような形状の成形品や
図4に示す中空体である三方管を長手方向に切断した図
3に示す形状の成形品等が挙げられる。
In the vibration-welded molded article made of a polyamide resin of the present invention, a plurality of parts are firstly molded using a polyamide resin composition. As a molding method of a molded article obtained by primary molding, a molding method generally used in molding of a thermoplastic resin is applied, and preferably, an injection molding method is used. The plurality of molded products obtained by the primary molding in the present invention may have the same shape or different shapes from each other, for example, a molded product having a shape as shown in FIG. 1 or a hollow body as shown in FIG. A molded product having a shape shown in FIG. 3 in which a three-way tube is cut in a longitudinal direction is exemplified.

【0018】次に、一次成形された複数の成形品をを振
動溶着により接合し、ポリアミド樹脂製振動溶着成形品
を得る。振動溶着における、振動の周波数は100〜3
00Hzであり、振幅は0.5〜2.0mmであり、好
ましくは0.8〜1.6mmである。溶着圧力は、5〜
100kg/cm2であり、好ましくは10〜60kg
/cm2のである。溶着圧力は、大きすぎても小さすぎ
ても、溶着強度が低下する。所定の圧力下にあるべき溶
着時間は、目的とする溶け代が得られるように設定し、
圧力を解放した後の保持時間は、溶着部が十分固化する
ように設定する。
Next, the plurality of primary molded products are joined by vibration welding to obtain a polyamide resin vibration welded molded product. The frequency of vibration in vibration welding is 100 to 3
00 Hz, and the amplitude is 0.5 to 2.0 mm, preferably 0.8 to 1.6 mm. The welding pressure is 5
100 kg / cm 2 , preferably 10 to 60 kg
/ Cm 2 . If the welding pressure is too high or too low, the welding strength will decrease. The welding time, which should be under a predetermined pressure, is set so that the desired melting allowance is obtained,
The holding time after releasing the pressure is set so that the welded portion is sufficiently solidified.

【0019】以下、本発明を実施例により更に詳細に説
明するが、本発明はその要旨を超えない限り、以下の実
施例に限定されるものではない。
Hereinafter, the present invention will be described in more detail with reference to examples. However, the present invention is not limited to the following examples unless it exceeds the gist of the present invention.

【実施例】以下の実施例及び比較例において使用したポ
リアミド樹脂は次の通りである。
The polyamide resins used in the following examples and comparative examples are as follows.

【0020】(1)ホモポリアミド樹脂−1:6ナイロ
ン(NOVAMID 1010J、相対粘度2.5、三
菱エンジニアリングプラスチックス株式会社製)と6ナ
イロン(NOVAMID 1020J、相対粘度3.
5、三菱エンジニアリングプラスチックス株式会社製)
とを混合し、相対粘度を3.2とした6ナイロン。 (2)ホモポリアミド樹脂−2:6ナイロン(NOVA
MID 1010J、相対粘度2.5、三菱エンジニア
リングプラスチックス株式会社製)と6ナイロン(NO
VAMID 1020J、相対粘度3.5、三菱エンジ
ニアリングプラスチックス株式会社製)とを混合し、相
対粘度を3.3とした6ナイロン。
(1) Homopolyamide resin-1: Nylon 6 (NOVAMID 1010J, relative viscosity 2.5, manufactured by Mitsubishi Engineering-Plastics Corporation) and Nylon 6 (NOVAMID 1020J, relative viscosity 3.
5. Mitsubishi Engineering Plastics Co., Ltd.)
6 nylon having a relative viscosity of 3.2. (2) Homopolyamide resin-2: 6 nylon (NOVA
MID 1010J, relative viscosity 2.5, manufactured by Mitsubishi Engineering-Plastics Corporation and 6 nylon (NO
6 nylon having a relative viscosity of 3.3 by mixing VAMID 1020J, relative viscosity 3.5, manufactured by Mitsubishi Engineering-Plastics Corporation.

【0021】(3)コポリアミド樹脂−1:6/66ナ
イロン(NOVAMID 2420J、融点193℃、
三菱エンジニアリングプラスチックス株式会社製) (4)コポリアミド樹脂−2:6/6Tナイロン(NO
VAMID 2620J、融点205℃、三菱エンジニ
アリングプラスチックス株式会社製) (5)コポリアミド樹脂−3:6I/6Tナイロン(N
OVAMID X21S04、非晶性ナイロン、三菱エ
ンジニアリングプラスチックス株式会社製) (6)ガラス繊維:商品名T249GH(日本電気硝子
株式会社製)
(3) Copolyamide resin-1: 6/66 nylon (NOVAMID 2420J, melting point 193 ° C.,
(Mitsubishi Engineering Plastics Co., Ltd.) (4) Copolyamide resin-2: 6 / 6T nylon (NO
(VAMID 2620J, melting point 205 ° C, manufactured by Mitsubishi Engineering-Plastics Corporation) (5) Copolyamide resin-3: 6I / 6T nylon (N
(OVAMID X21S04, amorphous nylon, manufactured by Mitsubishi Engineering-Plastics Co., Ltd.) (6) Glass fiber: Trade name T249GH (manufactured by NEC Corporation)

【0022】振動溶着強度の評価法は次の通りである。 (7)溶着強度測定用の試験片:後記実施例において説
明する条件で射出成形し、図−1に示す2つの同一形状
の一次成形品を得る。続いて、後記実施例において説明
する条件で振動溶着して、図−2に示す振動溶着成形品
を得た。 (8)溶着強度の測定法:この振動溶着成形品を、オリ
エンテック株式会社製テンシロンUTM−III−50
0型試験機を使用し、引張速度5mm/min、チャッ
ク間距離80mmの条件で引張り、溶着部における破断
強度を溶着強度とした。
The method for evaluating the vibration welding strength is as follows. (7) Test piece for measuring welding strength: Injection molding is performed under the conditions described in the examples described later to obtain two primary molded articles having the same shape as shown in FIG. Subsequently, vibration welding was performed under the conditions described in Examples described later to obtain a vibration welded molded product shown in FIG. (8) Measuring method of welding strength: This vibration-welded molded product is manufactured by Orientec Co., Ltd. using Tensilon UTM-III-50.
Using a 0-type testing machine, tension was applied under the conditions of a tensile speed of 5 mm / min and a distance between chucks of 80 mm, and the breaking strength at the welded portion was defined as the weld strength.

【0023】〔実施例1〜4〕表−1に記載のように、
ホモポリアミド樹脂、コポリアミド樹脂およびガラス繊
維を配合した。配合には、東芝機械株式会社製のTEM
−35B型二軸混練機を用い、設定温度280℃で溶融
混練した。得られたガラス繊維強化ポリアミド樹脂組成
物を、株式会社東芝機械プラスチックエンジニアリング
製のIS80EPN−2A型射出成形機を用いて、設定
温度260℃で、設定金型温度80℃で、図1に示す2
つの同一形状の一次成形品を得た。
Examples 1-4 As shown in Table 1,
A homopolyamide resin, a copolyamide resin and glass fiber were blended. The composition is TEM manufactured by Toshiba Machine Co., Ltd.
The mixture was melt-kneaded at a set temperature of 280 ° C. using a −35B type twin-screw kneader. The obtained glass fiber reinforced polyamide resin composition was heated at a set temperature of 260 ° C. and a set mold temperature of 80 ° C. using an IS80EPN-2A type injection molding machine manufactured by Toshiba Machine Plastic Engineering Co., Ltd.
Two primary molded articles of the same shape were obtained.

【0024】次に、この一次成形品の一対を、日本エマ
ソン株式会社製のVIBRATION WELDER
Model 2800 振動溶着機を使用して、周波数
240Hz、溶着圧力15.5kg/cm2、振幅1.5
mm、溶け代1.5mm、Hold圧力:振動停止後の
加圧力15.5kg/cm2、保持時間5.0secで溶
着して、図2に示す振動溶着成形品を得た。溶け代をコ
ントロールするのに日本エマソン株式会社製のCX13
2型非接触WDC溶着寸法制御装置を使用した。得られ
た振動溶着成形品の溶着強度の測定結果を表−1に示
す。
Next, a pair of the primary molded products was used as a VIBRATION WELDER manufactured by Emerson Japan.
Using a Model 2800 vibration welding machine, the frequency was 240 Hz, the welding pressure was 15.5 kg / cm 2 , and the amplitude was 1.5.
mm, welding margin 1.5 mm, Hold pressure: welding pressure 15.5 kg / cm 2 after stopping vibration, holding time 5.0 sec, to obtain a vibration welded molded product shown in FIG. CX13 made by Emerson Nippon to control melting allowance
A type 2 non-contact WDC welding size control device was used. Table 1 shows the measurement results of the welding strength of the obtained vibration welding molded product.

【0025】〔比較例1〕表−1に記載のように、ホモ
ポリアミド樹脂およびガラス繊維を配合した。配合に
は、東芝機械株式会社製のTEM−35B型二軸混練機
を用い、設定温度280℃で溶融混練した。得られたガ
ラス繊維強化ポリアミド樹脂組成物を用い、実施例1と
同様にして一次成形品および振動溶着成形品を得た。得
られた振動溶着成形品の溶着強度の測定結果を表−1に
示す。
Comparative Example 1 As shown in Table 1, a homopolyamide resin and glass fiber were blended. The mixture was melt-kneaded at a set temperature of 280 ° C. using a TEM-35B type twin-screw kneader manufactured by Toshiba Machine Co., Ltd. Using the obtained glass fiber reinforced polyamide resin composition, a primary molded product and a vibration weld molded product were obtained in the same manner as in Example 1. Table 1 shows the measurement results of the welding strength of the obtained vibration welding molded product.

【0026】〔比較例2〜3〕表−1に記載のように、
ホモポリアミド樹脂、コポリアミド樹脂およびガラス繊
維を配合した。配合には、東芝機械株式会社製のTEM
−35B型二軸混練機を用い、設定温度280℃で溶融
混練した。得られたガラス繊維強化ポリアミド樹脂組成
物を用い、実施例1と同様にして一次成形品および振動
溶着成形品を得た。得られた振動溶着成形品の溶着強度
の測定結果を表−1に示す。
[Comparative Examples 2-3] As shown in Table 1,
A homopolyamide resin, a copolyamide resin and glass fiber were blended. The composition is TEM manufactured by Toshiba Machine Co., Ltd.
The mixture was melt-kneaded at a set temperature of 280 ° C. using a −35B type twin-screw kneader. Using the obtained glass fiber reinforced polyamide resin composition, a primary molded product and a vibration weld molded product were obtained in the same manner as in Example 1. Table 1 shows the measurement results of the welding strength of the obtained vibration welding molded product.

【0027】[0027]

【表1】 [Table 1]

【0028】[0028]

【発明の効果】本発明のポリアミド樹脂製振動溶着成形
品は、強度、耐熱性、耐薬品性に優れ、且つ溶着強度に
著しく優れており、様々な分野の成形品に効果を発揮
し、特に高い安全性を要求される自動車用インテークマ
ニホールド等に有用である。
The vibration-welded molded article made of a polyamide resin of the present invention is excellent in strength, heat resistance, chemical resistance and remarkably excellent in welding strength, and is particularly effective for molded articles in various fields. It is useful for intake manifolds for automobiles that require high safety.

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

【図1】一次成形品の形状(60mm×25mm×4m
m)の例を示す説明図
FIG. 1 shows the shape of a primary molded product (60 mm × 25 mm × 4 m
Explanatory diagram showing an example of m)

【図2】振動溶着成形品の形状の例を示す説明図FIG. 2 is an explanatory view showing an example of the shape of a vibration welding molded product.

【図3】(a)、(b)は一対の中空体成形品の形状の
例を示す平面図
FIGS. 3A and 3B are plan views showing examples of shapes of a pair of hollow body molded products.

【図4】振動溶着中空体成形品の例を示す概念図FIG. 4 is a conceptual diagram showing an example of a vibration-welded hollow body molded product.

【符号の説明】[Explanation of symbols]

1 溶着面 2、2’ 上部開口部 3 下部開口部 DESCRIPTION OF SYMBOLS 1 Welding surface 2, 2 'Upper opening 3 Lower opening

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI B29L 22:00 23:00 (72)発明者 人見 達也 神奈川県平塚市東八幡5丁目6番2号 三 菱エンジニアリングプラスチックス株式会 社技術センター内────────────────────────────────────────────────── ─── Continued on the front page (51) Int.Cl. 6 Identification symbol FI B29L 22:00 23:00 (72) Inventor Tatsuya Hitomi 5-6-1 Higashi-Hachiman, Hiratsuka-shi, Kanagawa Mitsui Engineering Plastics Co., Ltd. Inside the company technology center

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 ホモポリアミド樹脂95〜50重量%と
コポリアミド樹脂5〜50重量%とからなるポリアミド
樹脂成分100重量部に対し、ガラス繊維10〜100
重量部を配合してなるポリアミド樹脂組成物を用いて一
次成形した複数の成形品を振動溶着してなるポリアミド
樹脂製振動溶着成形品。
1. A glass fiber of 10 to 100 parts by weight with respect to 100 parts by weight of a polyamide resin component comprising 95 to 50% by weight of a homopolyamide resin and 5 to 50% by weight of a copolyamide resin.
A vibration-welded molded article made of a polyamide resin obtained by vibration-welding a plurality of molded articles which are primarily molded using a polyamide resin composition containing parts by weight.
【請求項2】 ホモポリアミド樹脂が、6ナイロンであ
ることを特徴とする請求項1に記載のポリアミド樹脂製
振動溶着成形品。
2. The vibration welded product made of a polyamide resin according to claim 1, wherein the homopolyamide resin is 6 nylon.
【請求項3】 コポリアミド樹脂が、融点が180℃〜
220℃である結晶性コポリアミド樹脂、または非晶性
コポリアミド樹脂であることを特徴とする請求項1また
は2に記載のポリアミド樹脂製振動溶着成形品。
3. The copolyamide resin has a melting point of 180 ° C. or higher.
The vibration-welded molded article made of a polyamide resin according to claim 1 or 2, which is a crystalline copolyamide resin at 220 ° C or an amorphous copolyamide resin.
【請求項4】 コポリアミド樹脂が、6/66ナイロ
ン、6/6Tナイロンおよび6I/6Tナイロンから選
ばれる1種または複数種のコポリアミド樹脂であること
を特徴とする請求項1または2に記載のポリアミド樹脂
製振動溶着成形品。
4. The copolyamide resin according to claim 1, wherein the copolyamide resin is one or more copolyamide resins selected from 6/66 nylon, 6 / 6T nylon and 6I / 6T nylon. Vibration welding molded product made of polyamide resin.
【請求項5】 ポリアミド樹脂製振動溶着成形品が、中
空体成形品であることを特徴とする請求項1ないし4の
いずれかに記載のポリアミド樹脂製振動溶着成形品。
5. The vibration-welded molded article made of a polyamide resin according to claim 1, wherein the vibration-welded molded article made of a polyamide resin is a hollow body molded article.
JP13192497A 1997-05-22 1997-05-22 Polyamide resin vibration welding molding Pending JPH10315333A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13192497A JPH10315333A (en) 1997-05-22 1997-05-22 Polyamide resin vibration welding molding

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13192497A JPH10315333A (en) 1997-05-22 1997-05-22 Polyamide resin vibration welding molding

Publications (1)

Publication Number Publication Date
JPH10315333A true JPH10315333A (en) 1998-12-02

Family

ID=15069393

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13192497A Pending JPH10315333A (en) 1997-05-22 1997-05-22 Polyamide resin vibration welding molding

Country Status (1)

Country Link
JP (1) JPH10315333A (en)

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