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JP2002097334A - Resin composition, lighting fixture for vehicle using the same and method for producing the same - Google Patents

Resin composition, lighting fixture for vehicle using the same and method for producing the same

Info

Publication number
JP2002097334A
JP2002097334A JP2000285185A JP2000285185A JP2002097334A JP 2002097334 A JP2002097334 A JP 2002097334A JP 2000285185 A JP2000285185 A JP 2000285185A JP 2000285185 A JP2000285185 A JP 2000285185A JP 2002097334 A JP2002097334 A JP 2002097334A
Authority
JP
Japan
Prior art keywords
weight
lamp
parts
resin
resin composition
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
JP2000285185A
Other languages
Japanese (ja)
Other versions
JP4392973B2 (en
Inventor
Kenji Nishimoto
健志 西本
Takashi Matsumoto
崇 松本
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.)
Kanegafuchi Chemical Industry Co Ltd
Original Assignee
Kanegafuchi Chemical Industry Co Ltd
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 Kanegafuchi Chemical Industry Co Ltd filed Critical Kanegafuchi Chemical Industry Co Ltd
Priority to JP2000285185A priority Critical patent/JP4392973B2/en
Publication of JP2002097334A publication Critical patent/JP2002097334A/en
Application granted granted Critical
Publication of JP4392973B2 publication Critical patent/JP4392973B2/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
    • 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
    • B29C65/18Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure using heated tools
    • B29C65/20Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure using heated tools with direct contact, e.g. using "mirror"
    • 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
    • B29C66/114Single butt joints
    • B29C66/1142Single butt to butt 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
    • B29C66/01General 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
    • 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
    • B29C66/542Joining 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 joining hollow covers or hollow bottoms to open ends of container bodies
    • 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
    • B29C66/90Measuring or controlling the joining process
    • B29C66/91Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux
    • B29C66/914Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by controlling or regulating the temperature, the heat or the thermal flux
    • B29C66/9141Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by controlling or regulating the temperature, the heat or the thermal flux by controlling or regulating the temperature
    • B29C66/91421Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by controlling or regulating the temperature, the heat or the thermal flux by controlling or regulating the temperature of the joining tools
    • 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
    • B29C66/90Measuring or controlling the joining process
    • B29C66/91Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux
    • B29C66/914Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by controlling or regulating the temperature, the heat or the thermal flux
    • B29C66/9141Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by controlling or regulating the temperature, the heat or the thermal flux by controlling or regulating the temperature
    • B29C66/91431Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by controlling or regulating the temperature, the heat or the thermal flux by controlling or regulating the temperature the temperature being kept constant over time
    • 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
    • B29C66/80General aspects of machine operations or constructions and parts thereof
    • B29C66/83General aspects of machine operations or constructions and parts thereof characterised by the movement of the joining or pressing tools
    • B29C66/832Reciprocating joining or pressing tools
    • B29C66/8322Joining or pressing tools reciprocating along one axis
    • 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
    • B29L2031/30Vehicles, e.g. ships or aircraft, or body parts thereof
    • 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
    • B29L2031/747Lightning equipment

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Lining Or Joining Of Plastics Or The Like (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Graft Or Block Polymers (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a resin for lamp bodies for lighting fixture vehicle, capable of improving threading phenomenon of the resin constituting a lamp body caused when producing lighting fixture by joining the lamp body to lamp lens by a melting method by a hot plate and gloss of vacuum metallizing surface. SOLUTION: This thermoplastic resin composition is obtained by compounding a rubber-reinforced styrene-based resin consisting essentially of a graft copolymer of a specific rubber having a small particle diameter with a polycarbonate resin or a saturated polyester resin or further compounding the above compound with an antistatic agent.

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、車両灯具成形用樹
脂組成物、それを成形してなるランプボディ、リフレク
ター等車両灯具、それら灯具とランプレンズとを熱板融
着又は振動融着法により接合してなるランプケース等及
びその製造方法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a resin composition for molding a vehicle lamp, a lamp body formed by molding the same, a vehicle lamp such as a reflector, and a method of fusing these lamps and a lamp lens by hot plate fusion or vibration fusion. The present invention relates to a joined lamp case and the like and a method of manufacturing the same.

【0002】[0002]

【従来の技術】合成樹脂からなるランプボディとランプ
レンズとを接合する方法としては、接着剤で両者を固着
する方法もあるが、熱可塑性樹脂からなるランプボディ
に熱板を押し当てて溶融した後、溶融部分をメタクリル
酸メチル樹脂等からなるランプレンズに圧着する、いわ
ゆる熱板融着法が、溶剤をまったく使用しないことよる
コスト低減と作業環境改善の観点から採用されることが
増えてきた。しかしながら、このような熱板融着法で
は、ランプボディを構成する熱可塑性樹脂を熱板により
溶融した後、熱板を引き離す際に、溶融した樹脂が糸状
に引き伸ばされ(以下、この現象を「糸ひき」現象とい
う。)、これがランプレンズやランプポディ等車両灯具
の成形品表面に付着することにより外観不良となる不具
合が生じることがあった。この熱板融着法における糸引
き現象を改善する方法として、例えば、特開平9−12
902号公報には、ポリテトラフルオロエチレン等のフ
ッ素樹脂をポリカーボネート樹脂やABS樹脂等の熱可
塑性樹脂に対して添加し、ランプボディなどの灯具に成
形する方法が提案されている。
2. Description of the Related Art As a method for joining a lamp body made of a synthetic resin and a lamp lens, there is also a method of fixing the both with an adhesive, but a hot plate is pressed against a lamp body made of a thermoplastic resin and melted. Later, the so-called hot plate fusion method, in which the molten portion is pressed against a lamp lens made of methyl methacrylate resin or the like, has been increasingly adopted from the viewpoint of cost reduction and improvement of the working environment by not using a solvent at all. . However, in such a hot plate fusion method, after the thermoplastic resin constituting the lamp body is melted by the hot plate, when the hot plate is separated, the molten resin is stretched in a thread shape (hereinafter, this phenomenon is referred to as " This phenomenon is referred to as a "stringing" phenomenon.) When this adheres to the surface of a molded article of a vehicle lamp, such as a lamp lens or a lamp pod, there is a case where a defect such as poor appearance occurs. As a method for improving the stringing phenomenon in the hot plate fusion method, for example, Japanese Patent Application Laid-Open No. 9-12 / 1990
Japanese Patent Publication No. 902 proposes a method of adding a fluororesin such as polytetrafluoroethylene to a thermoplastic resin such as a polycarbonate resin or an ABS resin and molding the resultant into a lamp such as a lamp body.

【0003】また、車両灯具のランプボディ成形品内面
やレフレクター反射面には蒸着あるいはスパッタリング
等の加工が施される。この加工された成形品表面は、ラ
ンプの照度を反射するためのもので高い光沢が求められ
る。一般的に上記性能を得るために、まず、成形品にア
ンダーコートとよばれる下塗りを施した後、蒸着あるい
はスパッタリング等の加工が施される。
[0003] In addition, the inner surface of a molded lamp body of a vehicle lamp and the reflector reflecting surface are subjected to processing such as vapor deposition or sputtering. The surface of the processed molded article is for reflecting the illuminance of the lamp and is required to have high gloss. In general, in order to obtain the above performance, first, a molded article is coated with an undercoat called an undercoat, and then processed such as vapor deposition or sputtering.

【0004】一般に、蒸着あるいはスパッタリング加工
の前に加工性を助けるためにアンダーコート加工が施さ
れる。最近、製品のコストダウンを目的として、このア
ンダーコート工程を省略し、いわゆるアンダーコートレ
スにしたいという要求がある。現在のところ、100%
のポリカーボネート樹脂等で成形された車両灯具ランプ
ボディでは、上記光沢規格をクリアーしているが、製品
のコストダウン、衝撃強度の改善、成形性向上のため、
ゴム強化スチレン系樹脂を導入すると、その蒸着表面の
光沢が低下し、満足の得られるものではなかった。特開
平10−287802号公報に芳香族ポリカーボネート
とアクリル酸エステル系ゴム重合体を含むビニル共重合
体からなる樹脂組成物が、蒸着やスパッタリングの加工
性に良好と記載されているが、アンダーコートレスを満
足するまでの特性は得られていない。
[0004] Generally, an undercoating process is performed before the vapor deposition or sputtering process to assist the processability. Recently, there has been a demand to omit this undercoating step and reduce the so-called undercoating for the purpose of cost reduction of products. Currently, 100%
The vehicle lamp body made of polycarbonate resin etc. meets the above gloss standards, but to reduce product cost, improve impact strength, and improve moldability,
When a rubber-reinforced styrene-based resin was introduced, the gloss of the vapor-deposited surface was lowered, which was not satisfactory. JP-A-10-287802 describes that a resin composition comprising a vinyl copolymer containing an aromatic polycarbonate and an acrylate rubber polymer is excellent in processability of vapor deposition and sputtering, but it does not require undercoating. Are not obtained.

【0005】[0005]

【発明が解決しようとする課題】本発明者らは、上記の
問題点に鑑み、熱板融着法によりランプボディをランプ
レンズに接合して車両用灯具を製造する際のランプボデ
ィを構成する樹脂の糸ひきを抑制し、更に車両灯具ラン
プボディ成形品内面には蒸着あるいはスパッタリング等
の加工を施す際、アンダーコート工程を省略しても、1
00%ポリカーボネート樹脂を成形して得られた車両灯
具ランプボディと同等の表面光沢を発現し、蒸着あるい
はスパッタリングの加工性の低下を伴うことない成形材
料と成型方法を見出したものである。
SUMMARY OF THE INVENTION In view of the above problems, the present inventors have constructed a lamp body for manufacturing a vehicle lamp by joining a lamp body to a lamp lens by a hot plate fusion method. Resin stringing is suppressed, and when an inner surface of a molded article of a vehicle lamp lamp body is subjected to a process such as vapor deposition or sputtering, even if the undercoating step is omitted, it is possible to reduce
The present invention has found a molding material and a molding method which exhibit the same surface gloss as a vehicle lamp lamp body obtained by molding a 00% polycarbonate resin and do not cause a decrease in workability of vapor deposition or sputtering.

【0006】[0006]

【課題を解決するための手段】本発明者らは、上記の目
的を達成するべく鋭意検討した結果、特定の小粒子径ゴ
ム含有グラフト共重合体を必須成分とするゴム強化スチ
レン系樹脂とポリカーボネート樹脂又は飽和ポリエステ
ル樹脂からなる樹脂組成物あるいは、該樹脂組成物に対
して、帯電防止剤を特定比率で存在させた樹脂組成物
が、熱板融着法によりランプボディとランプレンズとを
接合して車両用灯具を製造する際の糸ひきを大幅に改善
し、かつ、ランプボディ成形品表面を蒸着あるいはスパ
ッタリングする際、アンダーコート工程を省略しても、
高い表面光沢を満足する蒸着面が得られることを見出し
本発明に到達した。
Means for Solving the Problems As a result of intensive studies to achieve the above object, the present inventors have found that a rubber-reinforced styrene-based resin containing a specific small-particle-diameter rubber-containing graft copolymer as an essential component and polycarbonate A resin composition comprising a resin or a saturated polyester resin, or a resin composition in which an antistatic agent is present in a specific ratio with respect to the resin composition is used to join the lamp body and the lamp lens by a hot plate fusion method. Significantly improved threading in the manufacture of vehicular lamps, and when vapor-depositing or sputtering the surface of the lamp body molded product, even if the undercoating step was omitted,
The inventors have found that a vapor-deposited surface satisfying high surface gloss can be obtained, and have reached the present invention.

【0007】即ち、本発明は (A).(a1)芳香族ビニル化合物30〜90重量%、シア
ン化ビニル化合物10〜40重量%、及びこれらと共重
合可能な単量体0〜30重量%の合計100重量%から
なる単量体混合物を重合してなり、メチルエチルケトン
可溶分の還元粘度(30℃、N,N−ジメチルホルムア
ミド溶液中)が0.3〜1.2dl/gであるスチレン
系共重合体0〜98重量部、 (a2)ジエン系ゴム重合体、アクリル系ゴム重合体、シリ
コーン系ゴム重合体、及びオレフィン系ゴム重合体の中
から選択される少なくとも1種のゴム重合体であって体
積平均粒径が60〜250nmであるゴム重合体(R
a)5〜90重量部の存在下に芳香族ビニル化合物10
〜90重量%、(メタ)アクリル酸エステル化合物、シ
アン化ビニル化合物の少なくとも1種の化合物10〜9
0重量%及びこれらと共重合可能な単量体0〜30重量
%の合計100重量%からなる単量体混合物10〜95
重量部を重合してなるグラフト共重合体100〜2重量
部及び (a3)ジエン系ゴム重合体、アクリル系ゴム重合体、シリ
コーン系ゴム重合体及びオレフィン系ゴム重合体の中か
ら選択される少なくとも1種のゴム重合体であって体積
平均粒径が260〜1000nmであるゴム重合体(R
b)15〜90重量部の存在下に芳香族ビニル化合物1
0〜90重量%,(メタ)アクリル酸エステル化合物、
シアン化ビニル化合物の少なくとも1種の化合物10〜
90重量%及びこれらと共重合可能な単量体0〜30重
量%の合計100重量%からなる単量体混合物10〜8
5重量部を重合してなるグラフト共重合体0〜30重量
部[(a1)、(a2)及び(a3)合わせて100重量部]からな
り、ゴム重合体含有量が5〜30重量%であるゴム強化
スチレン系樹脂10〜90重量部、及び (B).ポリカーボネート樹脂又は飽和ポリエステル樹脂
90〜10重量部[(A)と(B)合わせて100重量部]か
らなる車両灯具成形用樹脂組成物(請求項1)、グラフ
ト共重合体(2)の体積平均粒径が60〜150nmであ
る請求項1記載の樹脂組成物(請求項2)、請求項1記
載の樹脂組成物100重量部に対して、帯電防止剤を
0.1〜5重量部配合することを特徴とする車両成形用
帯電防止樹脂組成物(請求項3)、帯電防止剤が、アル
カンスルフォン酸塩、アルキルベンゼンスルフォン酸
塩、ポリアルキレングリコール、ポリアルキレングリコ
ール系共重合体又はポリエーテルエステルアミドである
請求項3記載の帯電防止樹脂組成物(請求項4)、車両
灯具がランプボディである請求項1記載の樹脂組成物
(請求項5)、請求項1記載の樹脂組成物を成形してな
る車両灯具(請求項6)、請求項1記載の樹脂組成物を
成形してなるランプボディ(請求項7)、請求項1記載
の樹脂組成物を成形してなるリフレクター(請求項
8)、請求項7記載のランプボディを用いた自動車用ヘ
ッドランプケース、ウィンカーケース、バックランプケ
ース又はストップランプケース(請求項9)、請求項7
記載のランプボディに、加熱した熱板を押し当てて溶融
した後、溶融部分をランプレンズに圧着してランプボデ
ィとランプレンズとを接合することを特徴とする車両用
灯具の製造方法(請求項10)、熱板を250〜500
℃に加熱して行う請求項10記載の車両用灯具の製造法
(請求項11)、ランプレンズとしてメタクリル酸メチ
ル樹脂製レンズを用いる請求項10又は11記載の車両
用灯具の製造方法(請求項12)、請求項7記載のラン
プボディに、加熱した熱板を押し当てて溶融した後、溶
融部分をランプレンズに圧着してランプボディとランプ
レンズとを接合してなる車両用灯具(請求項13)、及
びランプレンズとしてメタクリル酸メチル樹脂製レンズ
を用いてなる請求項13記載の車両用灯具(請求項1
4)に関する。
That is, the present invention relates to (A). (a1) A monomer mixture comprising a total of 100% by weight of 30 to 90% by weight of an aromatic vinyl compound, 10 to 40% by weight of a vinyl cyanide compound, and 0 to 30% by weight of a monomer copolymerizable therewith. 0 to 98 parts by weight of a styrene copolymer having a reduced viscosity (30 ° C., in an N, N-dimethylformamide solution) of 0.3 to 1.2 dl / g, which is obtained by polymerization of methyl ethyl ketone soluble component; ) A diene rubber polymer, an acrylic rubber polymer, a silicone rubber polymer, and at least one rubber polymer selected from olefin rubber polymers having a volume average particle diameter of 60 to 250 nm. A rubber polymer (R
a) Aromatic vinyl compound 10 in the presence of 5 to 90 parts by weight
To 90% by weight, at least one compound of a (meth) acrylate compound and a vinyl cyanide compound
0 to 30% by weight of a total of 100% by weight of a monomer mixture of 10 to 95%
100 to 2 parts by weight of a graft copolymer obtained by polymerizing parts by weight and (a3) at least one selected from a diene rubber polymer, an acrylic rubber polymer, a silicone rubber polymer and an olefin rubber polymer. One kind of rubber polymer having a volume average particle size of 260 to 1000 nm (R
b) Aromatic vinyl compound 1 in the presence of 15 to 90 parts by weight
0-90% by weight, (meth) acrylate compound,
At least one compound of vinyl cyanide compounds
A monomer mixture of 10 to 8 consisting of 90% by weight and a total of 100% by weight of 0 to 30% by weight of monomers copolymerizable therewith;
5 to 30 parts by weight of a graft copolymer obtained by polymerizing 5 parts by weight [100 parts by weight in total of (a1), (a2) and (a3)], and a rubber polymer content of 5 to 30% by weight. 10 to 90 parts by weight of a rubber-reinforced styrene resin, and (B). A volume average of the resin composition for molding vehicle lighting (Claim 1), comprising 90 to 10 parts by weight of a polycarbonate resin or a saturated polyester resin [100 parts by weight in total of (A) and (B)], and a graft copolymer (2). The resin composition according to claim 1, which has a particle diameter of 60 to 150 nm (claim 2), and 0.1 to 5 parts by weight of an antistatic agent per 100 parts by weight of the resin composition according to claim 1. The antistatic resin composition for molding a vehicle (Claim 3), wherein the antistatic agent is an alkane sulfonate, an alkylbenzene sulfonate, a polyalkylene glycol, a polyalkylene glycol-based copolymer or a polyetheresteramide. The antistatic resin composition according to claim 3 (claim 4), and the resin composition according to claim 1 (claim 5), wherein the vehicle lamp is a lamp body. A vehicle lamp formed by molding a product (claim 6), a lamp body formed by molding the resin composition according to claim 1 (claim 7), and a reflector formed by molding the resin composition according to claim 1 (Claim 8) An automobile headlamp case, a turn signal case, a back lamp case or a stop lamp case using the lamp body according to claim 7 (claim 9).
A method for manufacturing a vehicular lamp, characterized in that a heated hot plate is pressed against the lamp body to melt the lamp body, and then the fused part is pressed against a lamp lens to join the lamp body and the lamp lens. 10), hot plate 250-500
The method for manufacturing a vehicle lighting device according to claim 10, wherein the method is performed by heating to a temperature of ° C (claim 11), and the method for manufacturing a vehicle lighting device according to claim 10 or 11, wherein a lens made of methyl methacrylate resin is used as a lamp lens. (12) A vehicular lamp in which a heated hot plate is pressed against the lamp body according to claim 7 to melt it, and then the fused portion is pressed against a lamp lens to join the lamp body and the lamp lens. 13) The vehicle lamp according to claim 13, wherein a lens made of methyl methacrylate resin is used as the lamp lens.
Regarding 4).

【0008】[0008]

【発明の実施の形態】本発明で特に重要なのは、車両灯
具の成形に用いる樹脂組成物に配合する特定の小粒子径
ゴム含有グラフト共重合体(a2)である。本発明の樹脂
組成物はこの小粒子径ゴム含有グラフト共重合体を含む
ゴム強化スチレン系樹脂(A)とポリカーボネート樹脂又
は飽和ポリエステル樹脂(B)からなり、車両灯具成形品
とした際、内面には蒸着あるいはスパッタリング等の加
工を施す際加工性がよく、加工表面の光沢が高く、熱板
融着法によりランプボディをランプレンズに接合してラ
ンプケースを製造する際のランプボディを構成する樹脂
の糸ひき性の改善が著しい。本発明の樹脂組成物は、
(A).(a1)芳香族ビニル化合物30〜90重量%、シア
ン化ビニル化合物10〜40重量%、及びこれらと共重
合可能な単量体0〜30重量%の合計100重量%から
なる単量体混合物を重合してなり、メチルエチルケトン
可溶分の還元粘度(30℃、N,N−ジメチルホルムア
ミド溶液中)が0.3〜1.2dl/g であるスチレ
ン系共重合体0〜98重量部、 (a2)ジエン系ゴム重合体、アクリル系ゴム重合体、シリ
コーン系ゴム重合体、及びオレフィン系ゴム重合体の中
から選択される少なくとも1種のゴム重合体であって体
積平均粒径が60〜250nmであるゴム重合体(R
a)5〜90重量部の存在下に芳香族ビニル化合物10
〜90重量%、(メタ)アクリル酸エステル化合物、シ
アン化ビニル化合物の少なくとも1種の化合物10〜9
0重量%及びこれらと共重合可能な単量体0〜30重量
%の合計100重量%からなる単量体混合物10〜95
重量部を重合してなるグラフト共重合体100〜2重量
部及び (a3)ジエン系ゴム重合体、アクリル系ゴム重合体、シリ
コーン系ゴム重合体及びオレフィン系ゴム重合体の中か
ら選択される少なくとも1種のゴム重合体であって体積
平均粒径が260〜1000nmであるゴム重合体(R
b)15〜90重量部の存在下に芳香族ビニル化合物1
0〜90重量%,(メタ)アクリル酸エステル化合物、
シアン化ビニル化合物の少なくとも1種の化合物10〜
90重量%及びこれらと共重合可能な単量体0〜30重
量%の合計100重量%からなる単量体混合物10〜8
5重量部を重合してなるグラフト共重合体0〜30重量
部[(a1)、(a2)及び(a3)合わせて100重量部]からな
り、ゴム重合体含有量が5〜30重量%であるゴム強化
スチレン系樹脂10〜90重量部、及び (B).ポリカーボネート樹脂又は飽和ポリエステル樹脂
90〜10重量部[(A)と(B)合わせて100重量部]か
らなる。
DETAILED DESCRIPTION OF THE INVENTION Particularly important in the present invention is a specific small particle size rubber-containing graft copolymer (a2) to be added to a resin composition used for molding a vehicle lighting device. The resin composition of the present invention comprises a rubber-reinforced styrene-based resin (A) containing this small-particle-diameter rubber-containing graft copolymer and a polycarbonate resin or a saturated polyester resin (B). Has good workability when performing processing such as vapor deposition or sputtering, has a high gloss on the processed surface, and is a resin that forms the lamp body when manufacturing the lamp case by joining the lamp body to the lamp lens by hot plate fusion. The improvement in the threading property of the product is remarkable. The resin composition of the present invention,
(A). (a1) A monomer mixture comprising a total of 100% by weight of 30 to 90% by weight of an aromatic vinyl compound, 10 to 40% by weight of a vinyl cyanide compound, and 0 to 30% by weight of a monomer copolymerizable therewith. 0 to 98 parts by weight of a styrene copolymer having a reduced viscosity (30 ° C., in an N, N-dimethylformamide solution) of 0.3 to 1.2 dl / g, obtained by polymerization, ) A diene rubber polymer, an acrylic rubber polymer, a silicone rubber polymer, and at least one rubber polymer selected from olefin rubber polymers having a volume average particle diameter of 60 to 250 nm. A rubber polymer (R
a) Aromatic vinyl compound 10 in the presence of 5 to 90 parts by weight
To 90% by weight, at least one compound of a (meth) acrylate compound and a vinyl cyanide compound
0 to 30% by weight of a total of 100% by weight of a monomer mixture of 10 to 95%
100 to 2 parts by weight of a graft copolymer obtained by polymerizing parts by weight and (a3) at least one selected from a diene rubber polymer, an acrylic rubber polymer, a silicone rubber polymer and an olefin rubber polymer. One kind of rubber polymer having a volume average particle size of 260 to 1000 nm (R
b) Aromatic vinyl compound 1 in the presence of 15 to 90 parts by weight
0-90% by weight, (meth) acrylate compound,
At least one compound of vinyl cyanide compounds
A monomer mixture of 10 to 8 consisting of 90% by weight and a total of 100% by weight of 0 to 30% by weight of monomers copolymerizable therewith;
5 to 30 parts by weight of a graft copolymer obtained by polymerizing 5 parts by weight [100 parts by weight in total of (a1), (a2) and (a3)], and a rubber polymer content of 5 to 30% by weight. 10 to 90 parts by weight of a rubber-reinforced styrene resin, and (B). It is composed of 90 to 10 parts by weight of a polycarbonate resin or a saturated polyester resin [100 parts by weight in total of (A) and (B)].

【0009】前記スチレン系共重合体(a1)は、シアン化
ビニル化合物10〜40重量%、芳香族ビニル化合物3
0〜90重量%、及びこれらと共重合可能な単量体0〜
30重量%の合計100重量%からなる単量体を重合し
てなるが、より好ましくはシアン化ビニル化合物15〜
37重量%、芳香族ビニル化合物40〜90重量%、及
びこれらと共重合可能な単量体が0〜15重量%であ
る。
The styrenic copolymer (a1) comprises 10 to 40% by weight of a vinyl cyanide compound and 3
0 to 90% by weight and a monomer copolymerizable therewith
It is obtained by polymerizing 30% by weight of a total of 100% by weight of a monomer, more preferably a vinyl cyanide compound 15 to
37% by weight, 40 to 90% by weight of an aromatic vinyl compound, and 0 to 15% by weight of a monomer copolymerizable therewith.

【0010】前記シアン化ビニル化合物としては、アク
リロニトリル、メタクリロニトリル等が挙げられる。こ
れらは単独または2種以上を組み合わせて用いることが
できる。
Examples of the vinyl cyanide compound include acrylonitrile and methacrylonitrile. These can be used alone or in combination of two or more.

【0011】前記芳香族ビニル化合物としてはスチレ
ン、α−メチルスチレン、p−メチルスチレン、p−イ
ソプロピルスチレン、クロルスチレン、ブロモスチレン
等があげられる。
The aromatic vinyl compound includes styrene, α-methylstyrene, p-methylstyrene, p-isopropylstyrene, chlorostyrene, bromostyrene and the like.

【0012】共重合可能な単量体としては、マレイミ
ド、N−メチルマレイミド、N−エチルマレイミド、N
−プロピルマレイミド、N−ブチルマレイミド、N−フ
ェニルマレイミド、N−(p−メチルフェニル)マレイ
ミド等のマレイミド化合物、メチルメタクリレート、エ
チルメタクリレート、ブチルメタクリレート、2−エチ
ルヘキシルメタクリレート、ステアリルメタクリレート
等等の炭素数1〜18のアルキル基を有する少なくとも
1種のメタクリル酸エステル、メチルアクリレート、エ
チルアクリレート、ブチルアクリレート、2−エチルヘ
キシルアクリレート、ステアリルアクリレート等の炭素
数1〜18のアルキル基を有する少なくとも1種のアク
リル酸エステル、(メタ)アクリル酸、グリシジル(メ
タ)アクリレート、等の(メタ)アクリル酸エステル以
外の(メタ)アクリル酸誘導体等が挙げられる。これら
は、1種または2種以上の組み合わせで用いられる。
Examples of the copolymerizable monomer include maleimide, N-methylmaleimide, N-ethylmaleimide, and N-ethylmaleimide.
Maleimide compounds such as -propylmaleimide, N-butylmaleimide, N-phenylmaleimide and N- (p-methylphenyl) maleimide; At least one acrylate having an alkyl group having 1 to 18 carbon atoms such as at least one methacrylate having an alkyl group of 18 to 18, such as methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate and stearyl acrylate; , (Meth) acrylic acid, glycidyl (meth) acrylate, and other (meth) acrylic acid derivatives other than (meth) acrylic acid esters. These are used alone or in combination of two or more.

【0013】又、このスチレン系共重合体(a1)のメチル
エチルケトン可溶分の還元粘度(30℃、N,N−ジメ
チルホルムアミド溶液中)は0.3〜1.2dl/g、
更に好ましくは0.4〜0.9dl/gである。前記小
粒子径ゴム含有グラフト共重合体(a2)におけるゴム重合
体(Ra)の体積平均粒径は60〜250nmである
が、蒸着面の光沢の高い点から、好ましくは60〜15
0nmである。体積平均粒径が、60nm未満では衝撃
強度の低下が大きく、又250nmを越えると蒸着面の
光沢が低下する。
The reduced viscosity (30 ° C., in N, N-dimethylformamide solution) of the methyl ethyl ketone soluble portion of the styrenic copolymer (a1) is 0.3 to 1.2 dl / g.
More preferably, it is 0.4 to 0.9 dl / g. The volume average particle diameter of the rubber polymer (Ra) in the small particle diameter rubber-containing graft copolymer (a2) is from 60 to 250 nm.
0 nm. If the volume average particle size is less than 60 nm, the impact strength is greatly reduced, and if it exceeds 250 nm, the gloss of the deposition surface is reduced.

【0014】前記中粒子径ゴム含有グラフト共重合体(a
3)におけるゴム重合体(Rb)の体積平均粒径は260
〜1000nmであり、グラフト共重合体(a3)は蒸着面
の光沢性からは、使用しない方が好ましい。しかし、衝
撃向上のために、30重量部まで使用することができ、
蒸着面の光沢性から好ましくは0〜15重量部である。
The above-mentioned rubber-containing graft copolymer having a medium particle size (a
The volume average particle size of the rubber polymer (Rb) in 3) is 260
It is preferable that the graft copolymer (a3) is not used from the viewpoint of glossiness of the deposition surface. However, to improve the impact, it can be used up to 30 parts by weight,
The amount is preferably 0 to 15 parts by weight from the viewpoint of glossiness of the deposition surface.

【0015】前記のゴム重合体(Ra)、(Rb)とし
ては、ブタジエンゴム、スチレン−ブタジエンゴム、ア
クリロニトリル−ブタジエンゴム等のジエン系ゴム重合
体、アクリル酸ブチルゴム、ブタジエン−アクリル酸ブ
チルゴム、アクリル酸2−エチルヘキシル−アクリル酸
ブチルゴム、メタクリル酸2−エチルヘキシル−アクリ
ル酸ブチルゴム、アクリル酸ステアリル−アクリル酸ブ
チルゴム、ジメチルシロキサン−アクリル酸ブチルゴ
ム,シリコン系/アクリル酸ブチル複合ゴム等のアクリ
ル系ゴム重合体、エチレン−プロピレンゴム,エチレン
−プロピレン−ジエンゴム等のオレフィン系ゴム重合
体、ポリジメチルシロキサンゴム等のシリコン系ゴム重
合体が挙げられ、これらは単独または2種以上組み合わ
せて用いられる。
The rubber polymers (Ra) and (Rb) include diene rubber polymers such as butadiene rubber, styrene-butadiene rubber, acrylonitrile-butadiene rubber, butyl acrylate rubber, butadiene-butyl acrylate rubber, and acrylic acid. Acrylic rubber polymers such as 2-ethylhexyl-butyl acrylate rubber, 2-ethylhexyl methacrylate-butyl acrylate rubber, stearyl acrylate-butyl acrylate rubber, dimethylsiloxane-butyl acrylate rubber, silicone / butyl acrylate composite rubber, and ethylene Olefin rubber polymers such as propylene rubber and ethylene-propylene-diene rubber; and silicon rubber polymers such as polydimethylsiloxane rubber. These may be used alone or in combination of two or more.

【0016】前記グラフト共重合体(a2)及び(a3)におけ
る単量体混合物は、芳香族ビニル化合物10〜90重量
%,(メタ)アクリル酸エステル、シアン化ビニル化合
物の少なくとも1種の化合物10〜90重量%及びこれ
らと共重合可能な単量体0〜30重量%の合計100重
量%からなる。
The monomer mixture in the graft copolymers (a2) and (a3) comprises 10 to 90% by weight of an aromatic vinyl compound, at least one compound of a (meth) acrylate ester and a vinyl cyanide compound. To 90% by weight and 0 to 30% by weight of monomers copolymerizable therewith.

【0017】芳香族ビニル化合物としては、スチレン、
α−メチルスチレン、p−メチルスチレン、p−イソプ
ロピルスチレン、クロルスチレン、ブロムスチレン等が
挙げられる。
As the aromatic vinyl compound, styrene,
α-methylstyrene, p-methylstyrene, p-isopropylstyrene, chlorostyrene, bromostyrene and the like.

【0018】シアン化ビニル化合物としては、アクリロ
ニトリル、メタクリロニトリル等が挙げられる。(メ
タ)アクリル酸エステル化合物としては、メチルメタク
リレート、エチルメタクリレート、ブチルメタクリレー
ト、2−エチルヘキシルメタクリレート、ステアリルメ
タクリレート等の炭素数1〜18のアルキル基を有する
メタクリル酸エステル、メチルアクリレート、エチルア
クリレート、ブチルアクリレート、2−エチルヘキシル
アクリレート、ステアリルアクリレート等の炭素数1〜
18のアルキル基を有するアクリル酸エステルが挙げら
れる。
Examples of the vinyl cyanide compound include acrylonitrile and methacrylonitrile. Examples of the (meth) acrylate compound include methacrylate having an alkyl group having 1 to 18 carbon atoms, such as methyl methacrylate, ethyl methacrylate, butyl methacrylate, 2-ethylhexyl methacrylate, and stearyl methacrylate, methyl acrylate, ethyl acrylate, and butyl acrylate. , 2-ethylhexyl acrylate, stearyl acrylate, etc.
An acrylate having 18 alkyl groups is exemplified.

【0019】共重合可能なその他の単量体としては、
(メタ)アクリル酸、グリシジル(メタ)アクリレー
ト、等の(メタ)アクリル酸エステル以外の(メタ)ア
クリル酸誘導体およびマレイミド、N−フェニルマレイ
ミド等のマレイミド化合物等が挙げられる。これらは、
1種または2種以上あっても良い。
Other copolymerizable monomers include:
(Meth) acrylic acid derivatives other than (meth) acrylic acid esters such as (meth) acrylic acid and glycidyl (meth) acrylate, and maleimide compounds such as maleimide and N-phenylmaleimide. They are,
One or more kinds may be used.

【0020】本発明のゴム強化スチレン系樹脂のゴム重
合体(Ra)又は(Ra)と(Rb)合計の含有量がゴ
ム強化スチレン系樹脂(A)中5〜30重量%、好ましく
は5〜25重量%である。
The rubber-reinforced styrene resin of the present invention has a rubber polymer (Ra) or a total content of (Ra) and (Rb) of 5 to 30% by weight, preferably 5 to 30% by weight in the rubber reinforced styrene resin (A). 25% by weight.

【0021】本発明で用いるポリカーボネート樹脂は、
芳香族ポリカーボネート、脂肪族ポリカーボネート、脂
肪族−芳香族ポリカーボネート等を挙げることができ
る。一般には、2,2−ビス(4−オキシフェニル)ア
ルカン系、ビス(4−オキシフェニル)エーテル系、ビ
ス(4−オキシフェニル)スルホン、ビス(4−オキシ
フェニル)フルフィドまたはビス(4−オキシフェニ
ル)スルホキサイド系等のビスフェノール類からなる重
合体、もしくは共重合体であり、目的に応じてハロゲン
で置換された、ビスフェノール類を用いた重合体も含ま
れる。
The polycarbonate resin used in the present invention comprises:
Aromatic polycarbonate, aliphatic polycarbonate, aliphatic-aromatic polycarbonate and the like can be mentioned. Generally, 2,2-bis (4-oxyphenyl) alkane, bis (4-oxyphenyl) ether, bis (4-oxyphenyl) sulfone, bis (4-oxyphenyl) sulfide or bis (4-oxy) It is a polymer or copolymer composed of bisphenols such as phenyl) sulfoxide, and also includes a halogen-substituted bisphenol-based polymer as required.

【0022】本発明で用いる飽和ポリエステル樹脂は、
ポリエチレンテレフタレート、ポリプロピレンテレフタ
レート、ポリブチレンテレフタレート、ポリエチレンナ
フタレート、ポリブチレンナフタレート、ポリエチレン
−1,2−ビス(フェノキシ)エタン−4,4"-ジカル
ボキシレートなどのほか、ポリエチレンイソフタレート
/テレフタレート、ポリブチレンフタレート/イソフタ
レート、ポリブチレンテレフタレート/デカンジカルボ
キシレートなどの共重合ポリエステルが挙げられる。こ
れらのうち、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が好ましく使用できる。また上記ポ
リカーボネート樹脂と上記飽和ポリエステル樹脂は2種
以上の樹脂を併用することができ、目的の物性を得るた
めに適宜ブレンド量を決定すればよいが、耐熱性向上目
的には、ポリカーボネート系樹脂量の多いポリカーボネ
ート樹脂系が、耐薬品性向上目的には、飽和ポリエステ
ル系樹脂の量の多い飽和ポリエステル樹脂系のブレンド
が好ましい。
The saturated polyester resin used in the present invention is:
Polyethylene terephthalate, polypropylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, polybutylene naphthalate, polyethylene-1,2-bis (phenoxy) ethane-4,4 "-dicarboxylate, etc., as well as polyethylene isophthalate / terephthalate, poly Copolymerized polyesters such as butylene phthalate / isophthalate, polybutylene terephthalate / decane dicarboxylate, etc. Of these, polyethylene terephthalate and polybutylene terephthalate can be preferably used. More than one kind of resin can be used in combination, and the amount of blending may be appropriately determined in order to obtain desired physical properties. Sulfonate-based resin a large amount of polycarbonate resin is, the chemical resistance improvement purposes, blends of abundant saturated polyester resin, saturated polyester resin is preferable.

【0023】本発明に係る、車両灯具成形用樹脂組成物
は上記のようなゴム強化スチレン系樹脂(A)10〜90
重量部、より好ましくは20〜80重量部、ポリカーボ
ネート樹脂、飽和ポリエステル樹脂から選ばれた1種ま
たは2種の樹脂(B)90〜10重量部、より好ましくは
80〜20重量部の[(A)と(B)合わせて100重量部]
からなる熱可塑性樹脂組成物である。前記各共重合体の
配合割合が上記の範囲外では熱板融着時の糸引き改良効
果が小さく、成形品にアンダーコートレスで蒸着あるい
はスパッタリングした際の表面光沢が低下する。
The resin composition for molding a vehicle lamp according to the present invention comprises the rubber-reinforced styrene resin (A) 10 to 90 as described above.
Parts by weight, more preferably 20 to 80 parts by weight, 90 to 10 parts by weight of one or two kinds of resins (B) selected from polycarbonate resins and saturated polyester resins, more preferably 80 to 20 parts by weight [(A ) And (B) in total 100 parts by weight]
And a thermoplastic resin composition comprising: If the blending ratio of each copolymer is out of the above range, the effect of improving the stringing at the time of hot plate fusion is small, and the surface gloss of the molded article when deposited or sputtered without undercoating is reduced.

【0024】本発明の範囲の組成が得られれば、ゴム強
化スチレン系樹脂はいかなる重合法を用いて製造したも
のでもかまわない。例えば、公知の塊状重合法、溶液重
合法、懸濁重合法、乳化−懸濁重合法、乳化−塊状重合
法等、本発明の範囲内の組成に制御できれば、どの重合
法よって製造したものでもよい。又、本発明の範囲であ
れば、ゴム強化スチレン系樹脂はいかなる開始剤、連鎖
移動剤、乳化剤を用いて製造したものでもかまわない。
開始剤としては、過硫酸カリウム等の熱分解開始剤、F
e−還元剤−有機パーオキサイド等のレドックス系開始
剤等、公知の開始剤が使用できる。t−ドデシルメルカ
プタン、n−ドデシルメルカプタン、α−メチルスチレ
ンダイマー、テルピノレン等公知の連鎖移動剤が使用で
きる。乳化剤としてはオレイン酸ソーダ、パルミチン酸
ソーダ、ロジン酸ソーダ等の脂肪酸金属塩系乳化剤、ド
デシルベンゼンスルホン酸ソーダ、炭素数12〜20の
アルキルスルホン酸ソーダ、ジオクチルスルホコハク酸
ソーダ等のスルホン酸金属塩系乳化剤等の公知の乳化剤
が使用できる。小粒子ゴム含有グラフト共重合体(a2)及
び中粒子ゴム含有グラフト共重合体(a3)を製造する場
合、前記単量体混合物をゴム状重合体の存在下に、水性
媒体中、ラジカル開始剤で重合させればよい。その際、
前記グラフト重合させる単量体混合物は、混合物として
使用しても、又必要に応じ、分割して使用しても良い。
さらに前記単量体混合物の添加方法としては、一度に全
量を仕込んでも、また逐次添加しても良く、特に制限さ
れるものではない。
As long as the composition within the range of the present invention is obtained, the rubber-reinforced styrenic resin may be produced by any polymerization method. For example, a known bulk polymerization method, a solution polymerization method, a suspension polymerization method, an emulsion-suspension polymerization method, an emulsion-bulk polymerization method, and the like, as long as the composition can be controlled within the scope of the present invention, any one produced by any polymerization method can be used. Good. Further, within the scope of the present invention, the rubber-reinforced styrene-based resin may be one produced using any initiator, chain transfer agent, or emulsifier.
Examples of the initiator include a thermal decomposition initiator such as potassium persulfate;
Known initiators such as a redox initiator such as e-reducing agent-organic peroxide can be used. Known chain transfer agents such as t-dodecyl mercaptan, n-dodecyl mercaptan, α-methylstyrene dimer and terpinolene can be used. Examples of the emulsifier include fatty acid metal salt-based emulsifiers such as sodium oleate, sodium palmitate, and sodium rosinate; metal sulfonic acid salts such as sodium dodecylbenzenesulfonate, sodium alkylsulfonate having 12 to 20 carbon atoms, and sodium dioctylsulfosuccinate. A known emulsifier such as an emulsifier can be used. When producing the small particle rubber-containing graft copolymer (a2) and the medium particle rubber-containing graft copolymer (a3), in the presence of the rubber mixture of the monomer mixture, in an aqueous medium, a radical initiator May be polymerized. that time,
The monomer mixture to be graft-polymerized may be used as a mixture or, if necessary, dividedly.
Further, the method for adding the monomer mixture is not particularly limited, and the entire amount may be charged at once or may be added sequentially.

【0025】本発明のゴム強化スチレン系樹脂は製造方
法によって異なるが、例えば、これらを重合体ラテック
ス、スラリー、溶液、粉末、ペレットの状態、あるいは
これらの組み合わせにて混合して製造できる。ラテック
スからポリマー粉末を回収する場合は、通常の方法、例
えばラテックスに塩化カルシウム、塩化マグネシウム、
硫酸マグネシウムのようなアルカリ土類金属の塩、塩化
ナトリウム、硫酸ナトリウムのようなアルカリ金属の
塩、塩酸、硫酸、酢酸、リン酸のような無機酸及び有機
酸を添加することでラテックスを凝固した後、脱水乾燥
する方法で実施できる。又、スプレー乾燥法も使用でき
る。更に、安定剤の使用する量の一部を分散液の状態で
これら樹脂のラテックスあるいはスラリーに添加するこ
ともできる。
The rubber-reinforced styrene resin of the present invention varies depending on the production method. For example, it can be produced by mixing these in the form of a polymer latex, slurry, solution, powder, pellets, or a combination thereof. When recovering the polymer powder from the latex, the usual method, for example, calcium chloride, magnesium chloride in the latex,
The latex was coagulated by adding an alkaline earth metal salt such as magnesium sulfate, an alkali metal salt such as sodium chloride and sodium sulfate, and an inorganic acid and an organic acid such as hydrochloric acid, sulfuric acid, acetic acid, and phosphoric acid. Thereafter, it can be carried out by a method of dehydrating and drying. Also, a spray drying method can be used. Further, a part of the amount of the stabilizer used may be added to a latex or slurry of these resins in the form of a dispersion.

【0026】本発明の車両灯具用樹脂組成物であるゴム
強化スチレン系樹脂(A)とポリカーボネート樹脂あるい
は飽和ポリエステル樹脂(B)の各成分をブレンドする方
法は、例えばへンシェルミキサーやリボンブレンダー等
のブレンダーを用い、目的とする安定剤、酸化防止剤、
紫外線吸収剤、帯電防止剤、滑剤、顔料、無機充頃剤を
必要に応じて適宜使用することもできる。特に、帯電防
止剤は熱板融着時の糸引き防止改善に有効である。帯電
防止剤としては通常用いられる帯電防止剤が使用でき
る。なかでもアルカンスルホン酸塩、アルキルベンゼン
スルホン酸塩、ポリアルキレングリコール、ポリアルキ
レングリコール系共重合体あるいはポリエーテルエステ
ルアミドが熱板融着時の糸引き現象防止改善の効果が優
れている。
The method of blending the rubber-reinforced styrenic resin (A), which is the resin composition for vehicle lighting of the present invention, with the polycarbonate resin or the saturated polyester resin (B) can be performed, for example, by using a hen-shell mixer or a ribbon blender. Using a blender of the desired stabilizer, antioxidant,
UV absorbers, antistatic agents, lubricants, pigments, and inorganic fillers can be used as needed. In particular, the antistatic agent is effective for improving the prevention of stringing at the time of hot plate fusion. As the antistatic agent, a commonly used antistatic agent can be used. Among them, alkane sulfonates, alkylbenzene sulfonates, polyalkylene glycols, polyalkylene glycol-based copolymers or polyetheresteramides are excellent in the effect of preventing and improving the stringing phenomenon at the time of hot plate fusion.

【0027】また、フェノール系、イオウ系、リン系又
はヒンダードアミン系の安定剤、ベンゾフェノン系又は
ベンゾトリアゾール系の紫外線吸収剤、及びオルガノポ
リシロキサン、エチレンビスステアリン酸アマイド、脂
肪族炭化水素、高級脂肪酸と高級アルコールのエステル
等の滑剤等は成形用樹脂として、より高性能なものとす
るために用いることができる。これらの安定剤、滑剤
は、単独でも、また2種以上混合して使用することもで
きる。
Also, phenol-based, sulfur-based, phosphorus-based or hindered-amine-based stabilizers, benzophenone-based or benzotriazole-based ultraviolet absorbers, and organopolysiloxanes, ethylenebisstearic amides, aliphatic hydrocarbons and higher fatty acids Lubricants such as esters of higher alcohols and the like can be used as molding resins for higher performance. These stabilizers and lubricants can be used alone or in combination of two or more.

【0028】本発明では、上記のような熱可塑性樹脂組
成物から成形されたランプボディに加熱した熱板を押し
当てて溶融した後、溶融部分をランプレンズに圧着して
ランプボディとランプレンズとを接合して車両用灯具を
製造する。前記の場合の熱板の温度は、250〜500
℃に加熱して行うことが好ましい。250℃未満では接
着強度が不足し、500℃を越えると溶融が進みすぎて
作業性がわるくなる。また、前記ランプボディに接合さ
れるランプレンズとしては、レンズの透明性と強い接着
強度が得られる点で、メタクリル酸メチル樹脂を成形し
てえられるレンズを用いることが好ましい。
In the present invention, a heated hot plate is pressed against a lamp body molded from the thermoplastic resin composition as described above to melt it, and then the molten portion is pressed against a lamp lens to form a lamp body and a lamp lens. To manufacture a vehicular lamp. The temperature of the hot plate in the above case is 250 to 500
It is preferred to carry out by heating to ° C. If the temperature is lower than 250 ° C., the adhesive strength is insufficient. Further, as the lamp lens to be joined to the lamp body, it is preferable to use a lens obtained by molding a methyl methacrylate resin from the viewpoint that transparency and strong adhesive strength of the lens can be obtained.

【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、これら実施例は本発明を何ら限定するものでは
ない。尚、実施例の記載中で、特に断らない限り、
『部』は重量部を、『%』は重量%を表す。また、実施
中の各略称は、次の意味を有する。
The present invention will be described below in more detail with reference to examples, but these examples do not limit the present invention in any way. In the description of the examples, unless otherwise specified.
“Parts” represents parts by weight, and “%” represents weight%. The abbreviations being implemented have the following meanings.

【0030】AN:アクリロニトリル St:スチレン MMA:メチルメタアクリレート PMI:フェニルマレイミド CHP:クメンハイドロパーオキサイド tDM:t−ドテシルメルカプタン αMSt:α―メチルスチレン (1)スチレン系共重合体(a1)の製造 攪拌機、還流冷却器、窒素導入口、モノマー導入口及び
温度計の設置された反応器に下記の物質を仕込んだ。 純水 250部 ラウリン酸ソーダ 3部 ナトリウムホルムアルデヒドスルホキシレート 0.4部 硫酸第一鉄 0.0025部 エチレンジアミン四酢酸二ナトリウム 0.01部 反応器を攪拌しながら窒素気流下に60℃まで昇温させ
た。60℃に到達した後、表1に示すモノマー(I)を
仕込んだ。十分乳化させた後、表1に示すモノマー(I
I) を連続的に6時間で滴下添加し、添加終了後、60
℃で1時間攪拌を続けて重合を終了し、a11、a12、a13
及びa14を得た。
AN: acrylonitrile St: styrene MMA: methyl methacrylate PMI: phenylmaleimide CHP: cumene hydroperoxide tDM: t-dotecilmercaptan αMSt: α-methylstyrene (1) Production of styrene copolymer (a1) The following substances were charged into a reactor equipped with a stirrer, a reflux condenser, a nitrogen inlet, a monomer inlet, and a thermometer. Pure water 250 parts Sodium laurate 3 parts Sodium formaldehyde sulfoxylate 0.4 parts Ferrous sulfate 0.0025 parts Disodium ethylenediaminetetraacetate 0.01 parts Heating to 60 ° C under a nitrogen stream while stirring the reactor I let it. After the temperature reached 60 ° C., the monomers (I) shown in Table 1 were charged. After sufficient emulsification, the monomers (I
I) was continuously added dropwise over a period of 6 hours.
Stirring was continued at 1 ° C. for 1 hour to complete the polymerization. A11, a12, a13
And a14 were obtained.

【0031】[0031]

【表1】 (2)小粒子径ゴム含有グラフト共重合体(a2)及び中粒
子径ゴム含有グラフト共重合体(a3)の製造 公知の方法にて、下記ゴム状ラテックスを得た。尚、ラ
テックスの体積平均粒径は、四酸化オスミウム染色法等
による透過型電子顕微鏡写真を撮影し、ゴム状分散粒子
500〜1000個の粒子径を測定して平均粒子径を求
めた。又、粒子が楕円形をしている場合には、長径aと
短径bとの平均値、即ち(a+b)/2をもって、粒子
径とした。 PBd−1:ポリブタジエン 平均粒子径:100nm PBd−2:ポリブタジエン 平均粒子径:470nm SBR:スチレン-ブタジエンゴム(スチレン/ブタジエン重量比:25/75) 平均粒子径:100nm PBA:アクリルゴム(ブチルアクリレート/アリルメタクリレート重量比:99 /1) 平均粒子径:150nm 攪拌機、還流冷却器、窒素導入口、モノマー導入口及び
温度計の設置された反応器に下記の物質を仕込んだ。 純水 250部 ゴム状重合体 表2に記載した種類、量 ナトリウムホルムアルデヒドスルホキシレート 0.3部 硫酸第一鉄 0.0025部 エチレンジアミン四酢酸二ナトリウム 0.01部 反応器を攪拌しながら窒素気流下に60℃まで昇温させ
た。60℃に到達した後、表2に示す単量体混合物を連
続的に5時間で滴下し、添加終了後、さらに60℃で1
時間攪拌を続けて重合を終了し、a21、a22,a23及びa31
を得た。
[Table 1] (2) Production of small particle size rubber-containing graft copolymer (a2) and medium particle size rubber-containing graft copolymer (a3) The following rubbery latex was obtained by a known method. Incidentally, the volume average particle diameter of the latex was determined by taking a transmission electron micrograph by an osmium tetroxide staining method or the like, measuring the particle diameter of 500 to 1000 rubber-like dispersed particles, and calculating the average particle diameter. When the particles are elliptical, the average value of the major axis a and the minor axis b, that is, (a + b) / 2 was defined as the particle diameter. PBd-1: polybutadiene average particle diameter: 100 nm PBd-2: polybutadiene average particle diameter: 470 nm SBR: styrene-butadiene rubber (styrene / butadiene weight ratio: 25/75) average particle diameter: 100 nm PBA: acrylic rubber (butyl acrylate / Allyl methacrylate weight ratio: 99/1) Average particle size: 150 nm The following substances were charged into a reactor equipped with a stirrer, a reflux condenser, a nitrogen inlet, a monomer inlet, and a thermometer. Pure water 250 parts Rubbery polymer Type and amount described in Table 2 Sodium formaldehyde sulfoxylate 0.3 parts Ferrous sulfate 0.0025 parts Disodium ethylenediaminetetraacetate 0.01 parts Nitrogen stream while stirring the reactor The temperature was raised to 60 ° C. below. After the temperature reached 60 ° C., the monomer mixture shown in Table 2 was continuously added dropwise over 5 hours.
The polymerization is terminated by continuing stirring for a time, and a21, a22, a23 and a31
I got

【0032】[0032]

【表2】 (3)ゴム強化スチレン系樹脂(A)の製造 前記(1)、(2)で製造した共重合体を、それぞれラ
テックス状態で表3に記載した比率(固形分)で混合
し、この混合ラテックスに酸化防止剤を添加し、塩化カ
ルシウムで凝固させた後、加熱、脱水、水洗、乾燥して
ゴム強化スチレン系樹脂(パウダー)A1〜A8を得
た。
[Table 2] (3) Production of rubber-reinforced styrenic resin (A) The copolymers produced in the above (1) and (2) were mixed in a latex state at the ratio (solid content) shown in Table 3, and this mixed latex was mixed. An antioxidant was added to the mixture, and the mixture was coagulated with calcium chloride, and then heated, dehydrated, washed with water and dried to obtain rubber-reinforced styrene resins (powder) A1 to A8.

【0033】[0033]

【表3】 (4)車両灯具成形用樹脂組成物の製造 芳香族ポリカーボネート樹脂(PC)として出光化学株
式会社製タフロンA2200を用い、飽和ポリエステル
樹脂として市販のポリブチレンテレフタレート(PB
T、粘度平均分子量:31000)を用い、表4に示す
樹脂組成物100部に対して、フェノール系の抗酸化剤
0.3部(AO−20:旭電化工業株式会社製)、リン
系の安定剤0.3部(PEP−24G:旭電化工業株式
会社製)を共通の添加剤としてブレンドし、250℃の
温度で押出機(大阪精機株式会社製、40mmφ単軸押
出機)にてペレットを得た。得られたペレットを150
トン射出成形機(FANUC製)を使用し、250℃の
温度でASTMの1号ダンベルと図1に示すランプボデ
ィ製品を成形し、それを用いて糸引き性並びに真空蒸着
の評価を実施した。 (a)ダンベル試験片を用いての糸ひき性評価 350℃に加熱したアルミニウム製の平板に、射出成形
にて得られたASTM1号ダンベルを10kgf/cm
2の圧力で10秒間押しつけた後、このダンベルを50
0mm/分の速度で引き上げた時に溶融面に発生した糸
の長さ[cm]を測定した。 (b)ランプボディ製品を用いての糸引き性評価 射出成形にて得られた図1に示すランプボディ製品を熱
板融着機を用いて、融着温度350℃、10kg/cm
2の圧力でアルミニウム製の熱板に10秒間押しつけた
後、50mm/分の速度で引き上げた時に融着面に糸引
きが発生するかどうかを判定した。結果を表4に示す。
なお、ランプボディー製品による糸引き性評価は、次の
基準に従った。
[Table 3] (4) Production of Resin Composition for Molding Vehicle Lights Teflon A2200 manufactured by Idemitsu Chemical Co., Ltd. was used as an aromatic polycarbonate resin (PC), and commercially available polybutylene terephthalate (PB) was used as a saturated polyester resin.
T, viscosity average molecular weight: 31000), and 0.3 part of phenolic antioxidant (AO-20: manufactured by Asahi Denka Kogyo Co., Ltd.) and phosphorus-based to 100 parts of the resin composition shown in Table 4. 0.3 parts of stabilizer (PEP-24G: manufactured by Asahi Denka Kogyo Co., Ltd.) is blended as a common additive and pelletized at an extruder (40 mmφ single screw extruder manufactured by Osaka Seiki Co., Ltd.) at a temperature of 250 ° C. I got 150 pellets obtained
Using an injection molding machine (manufactured by FANUC), an ASTM No. 1 dumbbell and a lamp body product shown in FIG. 1 were molded at a temperature of 250 ° C., and the stringing property and vacuum deposition were evaluated using the same. (A) Evaluation of threading property using dumbbell test piece ASTM No. 1 dumbbell obtained by injection molding was applied to an aluminum flat plate heated to 350 ° C. at 10 kgf / cm.
After pressing for 10 seconds at a pressure of 2 , this dumbbell is
The length [cm] of the yarn generated on the melted surface when pulled up at a speed of 0 mm / min was measured. (B) Evaluation of stringiness using lamp body product The lamp body product shown in FIG. 1 obtained by injection molding was fused at 350 ° C. and 10 kg / cm using a hot plate fusion machine.
After pressing against a hot plate made of aluminum at a pressure of 2 for 10 seconds, it was determined whether or not stringing occurred on the fused surface when pulled up at a speed of 50 mm / min. Table 4 shows the results.
In addition, the evaluation of stringiness by a lamp body product was based on the following criteria.

【0034】 ○: 糸引きなし(0.5cm以下) △: 少し糸引きあり(0.5〜1.0cm) ×: 糸引きあり(1.0cm以上) (c)ランプボディ製品を用いての真空蒸着評価 射出成形にて得られた図1に示すランプボディ製品を真
空蒸着機に装着し、蒸着装置のルツボにアルミニウムを
所定量投入後、蒸着機を密閉し、真空ポンプを作動させ
てアルミニウムの厚さが0.1μmとなるように蒸着さ
せた。蒸着性の比較として、芳香族ポカーボネート(P
C)樹脂(タフロンA2200:出光石油化学株式会社
製)を用いてランプボディ製品を作成し、同様に真空蒸
着した。評価は次の基準に従った。
○: No stringing (0.5 cm or less) △: Slight stringing (0.5 to 1.0 cm) ×: Stringing (1.0 cm or more) (c) Using a lamp body product Vacuum evaporation evaluation The lamp body product shown in Fig. 1 obtained by injection molding was mounted on a vacuum evaporation machine, a predetermined amount of aluminum was put into a crucible of the evaporation apparatus, the evaporation machine was sealed, and the vacuum pump was operated to activate the aluminum. Was deposited so as to have a thickness of 0.1 μm. As a comparison of vapor deposition properties, aromatic pocarbonate (P
C) A lamp body product was prepared using a resin (Teflon A2200: manufactured by Idemitsu Petrochemical Co., Ltd.), and vacuum-deposited similarly. The evaluation was based on the following criteria.

【0035】 ◎: 光沢が非常に優れている ○: 光沢が優れている △: 光沢がよい ×: 光沢が悪い◎: Very excellent gloss ○: Excellent gloss △: Good gloss ×: Poor gloss

【0036】[0036]

【表4】 表4の結果から明らかなように、本発明によれば、従来
から使用されている比較例の樹脂組成物からなるランプ
ボディを用いた場合に比べて、熱板融着法における糸引
き並びに真空蒸着表面光沢が大幅に改善されている。
[Table 4] As is clear from the results in Table 4, according to the present invention, the stringing and the vacuum in the hot plate fusion method were compared with the case where the lamp body made of the resin composition of the comparative example conventionally used was used. The deposition surface gloss is greatly improved.

【0037】[0037]

【発明の効果】本発明によれば、特定の小粒子径ゴムの
グラフト共重合体を必須成分とするゴム強化スチレン系
樹脂とポリカーボネート樹脂、飽和ポリエステル樹脂か
ら選ばれた1種または2種の樹脂を配合してなる熱可塑
性樹脂組成物あるいは、更に特定の帯電防止剤を配合し
てなる熱可塑性樹脂組成物を用いる事で、従来からラン
プボディの材料として使用されている一般的な熱可塑性
樹脂を用いる場合に比べて、ランプボディに加熱した熱
板を押し当てて溶融した後、溶融部分をランプレンズに
圧着してランプボディとランプレンズとを接合して車両
用灯具を製造する際の、ランプボディを構成する樹脂の
糸引き性を大幅に改善し、かつ真空蒸着面の光沢も大幅
に改善しうるものであり、特にヘッドランプ、ウィンカ
ー、ストップランプなどの車両用灯具の製造に有用であ
る。
According to the present invention, one or two resins selected from a rubber-reinforced styrene-based resin, a polycarbonate resin and a saturated polyester resin containing a graft copolymer of a specific small particle diameter rubber as an essential component. By using a thermoplastic resin composition containing a resin or a thermoplastic resin composition further containing a specific antistatic agent, a general thermoplastic resin conventionally used as a material for a lamp body is used. Compared to the case of using, when a hot plate heated to the lamp body is pressed and melted, the fused portion is pressed against a lamp lens, and the lamp body and the lamp lens are joined to produce a vehicular lamp. It significantly improves the stringiness of the resin that makes up the lamp body, and can also significantly improve the gloss of the vacuum-deposited surface, especially for headlamps, turn signals, and stop runs. Useful in the manufacture of vehicular lamp, such as.

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

【図1】糸引き性並びに真空蒸着評価に用いたランプボ
ディ製品の断面図。
FIG. 1 is a cross-sectional view of a lamp body product used for evaluation of stringiness and vacuum deposition.

【符号の説明】[Explanation of symbols]

1 ランプボディ 2 ランプ 3 融着面 4 ランプレンズ 5 蒸着面 DESCRIPTION OF SYMBOLS 1 Lamp body 2 Lamp 3 Fusing surface 4 Lamp lens 5 Deposition surface

フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C08L 69/00 C08L 69/00 // B29L 31:30 B29L 31:30 Fターム(参考) 4F211 AD05 AH73 TA01 TC13 TC14 TD11 TN07 TQ01 4J002 BC06W BN06X BN06Y BN12X BN12Y BN16X BN16Y BN17X BN17Y CG01Z CG02Z CH025 CL085 EV256 FD105 FD106 4J026 AA11 AA45 AA67 AA68 AB44 BA05 BA27 BA31 DB04 GA01 GA08 Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat II (reference) C08L 69/00 C08L 69/00 // B29L 31:30 B29L 31:30 F term (reference) 4F211 AD05 AH73 TA01 TC13 TC14 TD11 TN07 TQ01 4J002 BC06W BN06X BN06Y BN12X BN12Y BN16X BN16Y BN17X BN17Y CG01Z CG02Z CH025 CL085 EV256 FD105 FD106 4J026 AA11 AA45 AA67 AA68 AB44 BA05 BA27 BA31 DB04 GA01 GA08

Claims (14)

【特許請求の範囲】[Claims] 【請求項1】 (A).(a1)芳香族ビニル化合物30〜9
0重量%、シアン化ビニル化合物10〜40重量%、及
びこれらと共重合可能な単量体0〜30重量%の合計1
00重量%からなる単量体混合物を重合してなり、メチ
ルエチルケトン可溶分の還元粘度(30℃、N,N−ジ
メチルホルムアミド溶液中)が0.3〜1.2dl/g
であるスチレン系共重合体0〜98重量部、 (a2)ジエン系ゴム重合体、アクリル系ゴム重合体、シリ
コーン系ゴム重合体、及びオレフィン系ゴム重合体の中
から選択される少なくとも1種のゴム重合体であって体
積平均粒径が60〜250nmであるゴム重合体(R
a)5〜90重量部の存在下に芳香族ビニル化合物10
〜90重量%、(メタ)アクリル酸エステル化合物、シ
アン化ビニル化合物の少なくとも1種の化合物10〜9
0重量%及びこれらと共重合可能な単量体0〜30重量
%の合計100重量%からなる単量体 混合物10〜95重量部を重合してなるグラフト共重合
体100〜2重量部及び (a3)ジエン系ゴム重合体、アクリル系ゴム重合体、シリ
コーン系ゴム重合体及びオレフィン系ゴム重合体の中か
ら選択される少なくとも1種のゴム重合体であって体積
平均粒径が260〜1000nmであるゴム重合体(R
b)15〜90重量部の存在下に芳香族ビニル化合物1
0〜90重量%,(メタ)アクリル酸エステル化合物、
シアン化ビニル化合物の少なくとも1種の化合物10〜
90重量%及びこれらと共重合可能な単量体0〜30重
量%の合計100重量%からなる単量体混合物10〜8
5重量部を重合してなるグラフト共重合体0〜30重量
部[(a1)、(a2)及び(a3)合わせて100重量部]からな
り、ゴム重合体含有量が5〜30重量%であるゴム強化
スチレン系樹脂10〜90重量部、及び (B).ポリカーボネート樹脂又は飽和ポリエステル樹脂
90〜10重量部[(A)と(B)合わせて100重量部]か
らなる車両灯具成形用樹脂組成物。
(A). (a1) Aromatic vinyl compound 30-9
0% by weight, 10 to 40% by weight of a vinyl cyanide compound, and 0 to 30% by weight of a monomer copolymerizable therewith.
A monomer mixture consisting of 00% by weight is polymerized, and the reduced viscosity (30 ° C., in N, N-dimethylformamide solution) of the methyl ethyl ketone soluble component is 0.3 to 1.2 dl / g.
(A2) at least one selected from the group consisting of a diene rubber polymer, an acrylic rubber polymer, a silicone rubber polymer, and an olefin rubber polymer. Rubber polymer (R) having a volume average particle size of 60 to 250 nm
a) Aromatic vinyl compound 10 in the presence of 5 to 90 parts by weight
To 90% by weight, at least one compound of a (meth) acrylate compound and a vinyl cyanide compound
100 to 2 parts by weight of a graft copolymer obtained by polymerizing 10 to 95 parts by weight of a monomer mixture consisting of 0% by weight and 0 to 30% by weight of a monomer copolymerizable therewith; a3) a diene-based rubber polymer, an acrylic-based rubber polymer, a silicone-based rubber polymer, and at least one rubber polymer selected from olefin-based rubber polymers having a volume average particle diameter of 260 to 1000 nm; A rubber polymer (R
b) Aromatic vinyl compound 1 in the presence of 15 to 90 parts by weight
0-90% by weight, (meth) acrylate compound,
At least one compound of vinyl cyanide compounds
A monomer mixture of 10 to 8 consisting of 90% by weight and a total of 100% by weight of 0 to 30% by weight of monomers copolymerizable therewith;
5 to 30 parts by weight of a graft copolymer obtained by polymerizing 5 parts by weight [100 parts by weight in total of (a1), (a2) and (a3)], and a rubber polymer content of 5 to 30% by weight. 10 to 90 parts by weight of a rubber-reinforced styrene resin, and (B). A resin composition for molding vehicle lighting, comprising 90 to 10 parts by weight of a polycarbonate resin or a saturated polyester resin [100 parts by weight in total of (A) and (B)].
【請求項2】 グラフト共重合体(2)の体積平均粒径が
60〜150nmである請求項1記載の樹脂組成物。
2. The resin composition according to claim 1, wherein the volume average particle size of the graft copolymer (2) is 60 to 150 nm.
【請求項3】 請求項1記載の樹脂組成物100重量部
に対して、帯電防止剤を0.1〜5重量部配合すること
を特徴とする車両成形用帯電防止樹脂組成物。
3. An antistatic resin composition for molding a vehicle, comprising 0.1 to 5 parts by weight of an antistatic agent with respect to 100 parts by weight of the resin composition according to claim 1.
【請求項4】帯電防止剤が、アルカンスルフォン酸塩、
アルキルベンゼンスルフォン酸塩、ポリアルキレングリ
コール、ポリアルキレングリコール系共重合体又はポリ
エーテルエステルアミドである請求項3記載の帯電防止
樹脂組成物。
4. The method according to claim 1, wherein the antistatic agent is an alkane sulfonate,
The antistatic resin composition according to claim 3, which is an alkylbenzene sulfonate, a polyalkylene glycol, a polyalkylene glycol-based copolymer or a polyetheresteramide.
【請求項5】車両灯具がランプボディである請求項1記
載の樹脂組成物。
5. The resin composition according to claim 1, wherein the vehicle lamp is a lamp body.
【請求項6】請求項1記載の樹脂組成物を成形してなる
車両灯具。
6. A vehicle lamp formed by molding the resin composition according to claim 1.
【請求項7】請求項1記載の樹脂組成物を成形してなる
ランプボディ。
7. A lamp body obtained by molding the resin composition according to claim 1.
【請求項8】請求項1記載の樹脂組成物を成形してなる
リフレクター。
8. A reflector obtained by molding the resin composition according to claim 1.
【請求項9】請求項7記載のランプボディを用いた自動
車用ヘッドランプケース、ウィンカーケース、バックラ
ンプケース又はストップランプケース。
9. A head lamp case, a turn signal case, a back lamp case or a stop lamp case for a vehicle using the lamp body according to claim 7.
【請求項10】請求項7記載のランプボディに、加熱し
た熱板を押し当てて溶融した後、溶融部分をランプレン
ズに圧着してランプボディとランプレンズとを接合する
ことを特徴とする車両用灯具の製造方法。
10. A vehicle characterized in that a heated hot plate is pressed against the lamp body according to claim 7 and melted, and then the fused portion is pressed against a lamp lens to join the lamp body and the lamp lens. Of manufacturing lighting fixtures.
【請求項11】熱板を250〜500℃に加熱して行う
請求項10記載の車両用灯具の製造法。
11. The method for manufacturing a vehicular lamp according to claim 10, wherein the hot plate is heated to 250 to 500 ° C.
【請求項12】ランプレンズとしてメタクリル酸メチル
樹脂製レンズを用いる請求項10又は11記載の車両用
灯具の製造方法。
12. The method for manufacturing a vehicular lamp according to claim 10, wherein a lens made of methyl methacrylate resin is used as the lamp lens.
【請求項13】請求項7記載のランプボディに、加熱し
た熱板を押し当てて溶融した後、溶融部分をランプレン
ズに圧着してランプボディとランプレンズとを接合して
なる車両用灯具。
13. A vehicular lamp comprising a lamp body according to claim 7, wherein a heated hot plate is pressed against the lamp body to melt it, and then the fused portion is pressed against a lamp lens to join the lamp body and the lamp lens.
【請求項14】ランプレンズとしてメタクリル酸メチル
樹脂製レンズを用いてなる請求項13記載の車両用灯
具。
14. The vehicular lamp according to claim 13, wherein a lens made of a methyl methacrylate resin is used as the lamp lens.
JP2000285185A 2000-09-20 2000-09-20 RESIN COMPOSITION FOR VEHICLE LAMP MOLDING, VEHICLE LAMP USING THE SAME, AND METHOD FOR PRODUCING THE SAME Expired - Fee Related JP4392973B2 (en)

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Application Number Priority Date Filing Date Title
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Cited By (7)

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Publication number Priority date Publication date Assignee Title
JP2004300324A (en) * 2003-03-31 2004-10-28 Nippon A & L Kk Resin composition for vibration fusion and lamp housing molded article of lighting fitting for vehicle
WO2005087866A1 (en) * 2004-03-15 2005-09-22 Kaneka Corporation Organopolysiloxane-containing graft copolymer composition
WO2006039110A1 (en) * 2004-09-29 2006-04-13 General Electric Company Method for reducing stringiness of a resinous composition during hot plate welding
JP2007077274A (en) * 2005-09-14 2007-03-29 Nippon A & L Kk Thermoplastic resin composition, material for vehicle lighting fixture and housing part for vehicle lighting fixture
JP2007191528A (en) * 2006-01-18 2007-08-02 Mitsubishi Rayon Co Ltd Thermoplastic resin composition, automotive lamp housing using the same, and automotive lamp
JP2009061750A (en) * 2007-09-10 2009-03-26 Kojima Press Co Ltd Decorative resin molded product and manufacturing method thereof
JP2019510105A (en) * 2016-12-28 2019-04-11 エルジー・ケム・リミテッド Thermoplastic resin composition, method for producing the same, and injection-molded article including the same

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004300324A (en) * 2003-03-31 2004-10-28 Nippon A & L Kk Resin composition for vibration fusion and lamp housing molded article of lighting fitting for vehicle
WO2005087866A1 (en) * 2004-03-15 2005-09-22 Kaneka Corporation Organopolysiloxane-containing graft copolymer composition
JPWO2005087866A1 (en) * 2004-03-15 2008-01-24 株式会社カネカ Organopolysiloxane-containing graft copolymer composition
WO2006039110A1 (en) * 2004-09-29 2006-04-13 General Electric Company Method for reducing stringiness of a resinous composition during hot plate welding
JP2008514466A (en) * 2004-09-29 2008-05-08 ゼネラル・エレクトリック・カンパニイ Method for reducing stringiness of resin composition during hot plate welding
JP2007077274A (en) * 2005-09-14 2007-03-29 Nippon A & L Kk Thermoplastic resin composition, material for vehicle lighting fixture and housing part for vehicle lighting fixture
JP2007191528A (en) * 2006-01-18 2007-08-02 Mitsubishi Rayon Co Ltd Thermoplastic resin composition, automotive lamp housing using the same, and automotive lamp
JP2009061750A (en) * 2007-09-10 2009-03-26 Kojima Press Co Ltd Decorative resin molded product and manufacturing method thereof
US9364860B2 (en) 2007-09-10 2016-06-14 Kojima Industries Corporation Decorated resin molded article and method for producing the same
JP2019510105A (en) * 2016-12-28 2019-04-11 エルジー・ケム・リミテッド Thermoplastic resin composition, method for producing the same, and injection-molded article including the same
US11084921B2 (en) 2016-12-28 2021-08-10 Lg Chem, Ltd. Thermoplastic resin composition, method of preparing the same, and injection-molded article including the same

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