JPH05166498A - Beam lamp with front-glass - Google Patents

Beam lamp with front-glass

Info

Publication number
JPH05166498A
JPH05166498A JP35130991A JP35130991A JPH05166498A JP H05166498 A JPH05166498 A JP H05166498A JP 35130991 A JP35130991 A JP 35130991A JP 35130991 A JP35130991 A JP 35130991A JP H05166498 A JPH05166498 A JP H05166498A
Authority
JP
Japan
Prior art keywords
adhesive
windshield
heat resistance
component
beam lamp
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
JP35130991A
Other languages
Japanese (ja)
Other versions
JP3257812B2 (en
Inventor
Masanori Toya
正則 戸矢
Takeru Tamura
長 田村
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.)
Momentive Performance Materials Japan LLC
Original Assignee
Toshiba Silicone 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 Toshiba Silicone Co Ltd filed Critical Toshiba Silicone Co Ltd
Priority to JP35130991A priority Critical patent/JP3257812B2/en
Publication of JPH05166498A publication Critical patent/JPH05166498A/en
Application granted granted Critical
Publication of JP3257812B2 publication Critical patent/JP3257812B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To provide a beam lamp with a front-glass having no problem in outer appearance and having a very excellent adhesion between a front glass and a mirror, in which, particularly in case the adhesive agent having a low content of low molecular weight siloxane is used, the adhesion is excellent and the frosting of the front glass is prevented. CONSTITUTION:A front glass 6 is bonded using a colorless or minutely colored addition reaction type silicon adhesive agent containing a heat-resistance improver.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、フロントガラス付のハ
ロゲン電球ビームランプなどの改良に関し、さらに詳し
く、前面のフロントガラスなどとミラーとの接着に用い
られる接着剤が改良されたビームランプに関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an improvement in a halogen lamp beam lamp with a windshield, and more particularly to a beam lamp in which an adhesive used for adhering a front windshield and the like to a mirror is improved.

【0002】[0002]

【従来の技術】近年、ダイクロイックミラー付きハロゲ
ンランプ電球のようなビームランプに、安全性と紫外線
防止を目的として、フロントガラスを付けたものが増加
している。フロントガラスとダイクロイックミラーとの
間の接着には、従来からエポキシ系接着剤、縮合型シリ
コーン接着剤などが使用されていた。フロントガラス付
きのビームランプは、それ自体がほぼ密閉構造になるた
め、フロントガラスの無い場合に比べて内部の温度上昇
が激しく、接着剤部分の温度が250℃程度になるもの
もある。従来のエポキシ系接着剤の場合、耐熱性、耐紫
外線性が十分でないため、とくに高電力タイプでは、接
着剤が劣化し、フロントガラスがはずれるなどの、信頼
性に欠けるという欠点があった。
2. Description of the Related Art In recent years, beam lamps such as halogen lamp bulbs with dichroic mirrors, which are equipped with a windshield for the purpose of safety and prevention of ultraviolet rays, are increasing in number. For the adhesion between the windshield and the dichroic mirror, an epoxy adhesive, a condensation type silicone adhesive or the like has been conventionally used. Since the beam lamp with a windshield itself has a substantially sealed structure, the temperature inside the beam lamp may rise more sharply than in the case without the windshield, and the temperature of the adhesive portion may reach about 250 ° C in some cases. In the case of conventional epoxy adhesives, heat resistance and ultraviolet resistance are not sufficient. Therefore, particularly in the high power type, there is a drawback that the adhesive deteriorates and the windshield comes off, resulting in lack of reliability.

【0003】通常の縮合型シリコーン系でも同様な問題
があるが、エポキシ系に比べれば多少の向上はある。縮
合系シリコーン系の中でも250℃の耐熱性に優れたも
のもあるが、縮合型シリコーン接着剤は空気中の水蒸気
と反応して常温で硬化するものであるため、硬化して接
着性が発現するまでには時間がかかるという作業上の問
題と、硬化の際に発生する低分子量化合物が残留し、長
時間点灯すると気化してフロントガラスに付着し、白い
曇りが生じるという問題があった。
Although ordinary condensation type silicones have the same problem, they are slightly improved as compared with epoxy type. Among the condensation silicone type, some have excellent heat resistance at 250 ° C., but since the condensation type silicone adhesive reacts with water vapor in the air and cures at room temperature, it cures and exhibits adhesiveness. There is a problem in that it takes a long time to work, and a low-molecular weight compound generated during curing remains, vaporizes and adheres to the windshield after long-time lighting, and white fog occurs.

【0004】そこで本発明者らは、さきに、これらの問
題を解決するために、酸化鉄を配合した付加型シリコー
ン接着剤を用いることにより、上記の問題を解決するこ
とを見出した(特願平2−145846号)が、耐熱性
を付与するために配合した酸化鉄のために、外観がベン
ガラ色となり、塗布面が異常に目立つという問題があ
り、無彩色または微彩色の接着剤の開発が望まれてい
た。また低分子シロキサンの揮発により、長期間点灯す
るとフロントガラスの内面が曇るという問題は、かなり
解消されたとはいえ、さらに改良が望まれていた。
Therefore, the present inventors have previously found that, in order to solve these problems, an addition type silicone adhesive compounded with iron oxide is used to solve the above problems (Japanese Patent Application No. 2000-242242). No. 2-145846) has a problem that the iron oxide blended to impart heat resistance causes the appearance to be reddish-colored and the coated surface to be noticeably abnormal. Therefore, the development of an achromatic or fine-colored adhesive Was desired. Further, although the problem that the inner surface of the windshield becomes cloudy when the lamp is lit for a long time due to the volatilization of the low-molecular-weight siloxane has been largely solved, further improvement is desired.

【0005】[0005]

【発明が解決しようとする課題】本発明の目的は、上記
の問題を解決するよう、フロントガラスとミラーの間に
外観および耐熱性に優れ、しかも曇りの原因を生じない
接着剤層を有するビームランプを提供することである。
SUMMARY OF THE INVENTION An object of the present invention is to solve the above problems by providing a beam having an adhesive layer between the windshield and the mirror, which has excellent appearance and heat resistance and does not cause fog. Is to provide a lamp.

【0006】[0006]

【課題を解決するための手段】本発明者らは、この目的
を達成するために鋭意研究を重ねた結果、耐熱向上剤を
含有し、しかも無彩色または微彩色を呈する付加型接着
剤を用いることで、この問題を解決して、ビームランプ
の外観と特性を大幅に改良できることを見出し、本発明
を完成するに至った。
Means for Solving the Problems As a result of intensive studies to achieve this object, the present inventors have used an addition type adhesive containing a heat resistance improver and exhibiting an achromatic color or a faint color. As a result, it has been found that the problem can be solved and the appearance and characteristics of the beam lamp can be greatly improved, and the present invention has been completed.

【0007】すなわち本発明のビームランプは、耐熱性
向上剤を含有する無彩色または微彩色の付加反応型シリ
コーン接着剤でフロントガラスが接着されていることを
特徴とする。
That is, the beam lamp of the present invention is characterized in that the windshield is adhered by an achromatic or microchromatic addition reaction type silicone adhesive containing a heat resistance improver.

【0008】本発明で用いられる付加型シリコーン接着
剤は、基本的に、次の成分を配合した無彩色または微彩
色の組成物であり、硬化して接着剤層を形成するもので
ある。 (A)ケイ素原子に結合するビニル基を含有するポリオ
ルガノシロキサンベースポリマー; (B)ケイ素原子に結合する水素原子を含有するポリオ
ルガノハイドロジェンシロキサン架橋剤; (C)硬化触媒 (D)接着性付与剤;および (E)耐熱性向上剤。
The addition type silicone adhesive used in the present invention is basically an achromatic or finely colored composition containing the following components and is cured to form an adhesive layer. (A) a polyorganosiloxane base polymer containing a vinyl group bonded to a silicon atom; (B) a polyorganohydrogensiloxane crosslinker containing a hydrogen atom bonded to a silicon atom; (C) a curing catalyst (D) adhesiveness An imparting agent; and (E) a heat resistance improver.

【0009】上記の基本成分のほかに、目的に応じて、
無彩色または微彩色という外観を損なわない範囲で、任
意の充填剤、添加剤などを配合しても差支えない。
In addition to the above basic components, depending on the purpose,
Any filler, additive, etc. may be blended within a range that does not impair the achromatic or finely colored appearance.

【0010】ここに無彩色とは、透明または半透明の無
色をはじめ、白色、灰白色、灰色、灰黒色、黒色など、
特定の波長の可視光の選択的な反射を伴わない色調を言
い、微彩色とは、それらに若干の他の彩色を伴ってはい
るが、外観上とくに問題にならない範囲の色で、アイボ
リー系、水色系の色や;赤み・緑み・黄み・青みなどを
帯びた白色・灰白色・灰色・灰黒色・黒色が例示され
る。本発明の効果の点から、無色または白色〜灰色の明
度のものが好ましい。
The achromatic color includes transparent or translucent colorless, white, gray white, gray, gray black, black, etc.
It refers to a color tone that does not cause selective reflection of visible light of a specific wavelength, and a fine color is a color that, although accompanied by some other color, is in a range that does not matter in appearance and is ivory-based. , Light blue colors; white, gray white, gray, gray black, and black with reddish, greenish, yellowish, bluish, etc. are exemplified. From the viewpoint of the effect of the present invention, colorless or white to gray lightness is preferable.

【0011】付加型シリコーン接着剤を構成する(A)
成分のポリオルガノシロキサンベースポリマーは、ケイ
素原子に結合するビニル基を1分子に少なくとも2個有
するものである。分子中のビニル基の量が2個よりも少
ないと、架橋に関与しないポリオルガノシロキサンを生
じて、硬化して得られた組成物がゴム状弾性体にならな
い。(A)のポリオルガノシロキサンのケイ素原子に結
合する有機基のうち、前記のビニル基以外の基として
は、メチル、エチル、プロピル、ブチルなどのアルキル
基;シクロヘキシルなどのシクロアルキル基;フェニル
基;クロロメチル基、トリフルオロプロピル基などの置
換1価炭化水素基が例示されるが、合成の容易なこと、
未硬化の状態の取り扱が容易なこと、および硬化後の良
好な物理特性を保持するために必要なポリオルガノシロ
キサンの重合度を得やすい点から、メチル基が好まし
い。(A)で示されるポリオルガノシロキサンは、合成
の容易なことから実質的に直鎖状であることが好ましい
が、とくに機械的性質を向上させるために、一部または
全部として、分岐状で、末端にビニル基を有するものを
用いてもよい。硬化前の組成物の作業性と、硬化後の接
着剤の物性、とくにその機械的強度から、25℃におけ
る粘度が50〜100,000cSt の範囲であることが
好ましい。
Constituting Addition Type Silicone Adhesive (A)
The component polyorganosiloxane base polymer has at least two vinyl groups bonded to silicon atoms in one molecule. If the amount of vinyl groups in the molecule is less than 2, polyorganosiloxane that does not participate in crosslinking is formed, and the composition obtained by curing does not become a rubber-like elastic body. Of the organic groups bonded to the silicon atom of the polyorganosiloxane of (A), the groups other than the vinyl group include alkyl groups such as methyl, ethyl, propyl, and butyl; cycloalkyl groups such as cyclohexyl; phenyl groups; Substituted monovalent hydrocarbon groups such as chloromethyl group and trifluoropropyl group are exemplified, but it is easy to synthesize,
A methyl group is preferred because it is easy to handle the uncured state and the degree of polymerization of the polyorganosiloxane required to maintain good physical properties after curing is easily obtained. The polyorganosiloxane represented by (A) is preferably substantially linear because it is easy to synthesize, but in order to improve the mechanical properties, it may be partially or wholly branched. You may use what has a vinyl group at the terminal. From the workability of the composition before curing and the physical properties of the adhesive after curing, especially its mechanical strength, the viscosity at 25 ° C. is preferably in the range of 50 to 100,000 cSt.

【0012】(B)成分のポリオルガノハイドロジェン
シロキサン架橋剤は、(A)のポリオルガノシロキサン
のビニル基と反応してゴム状硬化物を形成するものであ
る。網状構造の高分子ポリシロキサンを得るために、
(B)成分はケイ素原子に結合する水素原子を1分子中
に少なくとも3個含有することが必要である。ケイ素原
子に結合する有機基としては、前述の(A)成分におけ
る有機基と同様の基が例示されるが、合成の容易さから
メチル基が最も好ましい。また、ビニル基のようなアル
ケニル基が存在していてもよい。このようなポリオルガ
ノハイドロジェンシロキサンは、シロキサン骨格が直鎖
状、分岐状および環状のいずれであってもよく、また、
これらの混合物であってもよい。(B)成分の配合量
は、(A)成分のポリオルガノシロキサンのビニル基1
個に対し、(B)成分中のケイ素原子に結合した水素原
子が0.5〜4個になるような量が好ましく、両成分の
重量比は、(A)成分100重量部に対し、0.01〜
10重量部の範囲が一般的である。(B)成分中の水素
原子の量が過大または過小の場合には、硬化後の接着剤
は十分な機械的性質や熱安定性が得られない。
The polyorganohydrogensiloxane crosslinking agent as the component (B) reacts with the vinyl group of the polyorganosiloxane as the component (A) to form a rubber-like cured product. In order to obtain a high molecular weight polysiloxane,
The component (B) must contain at least three hydrogen atoms bonded to silicon atoms in one molecule. Examples of the organic group bonded to the silicon atom include the same groups as the organic groups in the component (A) described above, but a methyl group is most preferable because of ease of synthesis. Moreover, an alkenyl group such as a vinyl group may be present. Such a polyorganohydrogensiloxane may have a linear, branched or cyclic siloxane skeleton, and
It may be a mixture of these. The blending amount of the component (B) is the vinyl group 1 of the polyorganosiloxane of the component (A).
The amount is preferably 0.5 to 4 hydrogen atoms bonded to silicon atoms in the component (B), and the weight ratio of both components is 0 relative to 100 parts by weight of the component (A). .01-
A range of 10 parts by weight is common. If the amount of hydrogen atoms in the component (B) is too large or too small, the cured adhesive will not have sufficient mechanical properties and thermal stability.

【0013】(C)成分の硬化触媒は、ビニル基とヒド
ロシリル基との間の付加反応に用いられる触媒である。
このような触媒としては、白金、ロジウムまたはパラジ
ウムの単体もしくは化合物があるが、触媒効果および取
組の容易さから、白金化合物が好ましい。白金化合物と
しては、塩化白金酸およびそのアルコール溶液、塩化白
金酸とアルコールとの錯体、塩化白金酸のビニルシロキ
サン錯体が例示される。分散性の問題から塩化白金酸の
溶液またはビニルシロキサン錯体が望ましい。(C)成
分の配合量は(A)成分と(B)成分の合計量に対し、
0.1〜1000ppm になる量が好ましい。
The curing catalyst of the component (C) is a catalyst used for an addition reaction between a vinyl group and a hydrosilyl group.
Examples of such a catalyst include platinum, rhodium, and palladium as a simple substance or a compound, but a platinum compound is preferable from the viewpoint of catalytic effect and easiness of work. Examples of the platinum compound include chloroplatinic acid and its alcohol solution, a complex of chloroplatinic acid and an alcohol, and a vinylsiloxane complex of chloroplatinic acid. A solution of chloroplatinic acid or a vinylsiloxane complex is desirable from the viewpoint of dispersibility. The blending amount of the component (C) is based on the total amount of the components (A) and (B).
An amount of 0.1 to 1000 ppm is preferable.

【0014】(D)成分の接着性付与剤としては、次の
ような複数の官能基が同一分子内に組み合わされて存在
するシラン誘導体やシロキサン誘導体が好ましい。 Si−H結合とエポキシ基; Si−H結合とアルコキシ基、またはそれに加えて
エステル結合; ビニル基および/またはエポキシ基とアルコキシ
基; アリル基とアルコキシ基; (メタ)アクリルオキシ基とアルコキシ基
As the adhesiveness-imparting agent of the component (D), a silane derivative or a siloxane derivative having the following plural functional groups combined in the same molecule is preferable. Si-H bond and epoxy group; Si-H bond and alkoxy group, or in addition ester bond; Vinyl group and / or epoxy group and alkoxy group; Allyl group and alkoxy group; (Meth) acryloxy group and alkoxy group

【0015】これらの官能基を有する化合物として、下
記の式(I)〜式(VI) のような化合物が挙げられる。
ただし、式中、Meはメチル基を表す。
Examples of compounds having these functional groups include compounds represented by the following formulas (I) to (VI).
However, in the formula, Me represents a methyl group.

【0016】[0016]

【化1】 [Chemical 1]

【0017】[0017]

【化2】 [Chemical 2]

【0018】(D)成分の配合量は、(A)成分100
重量部に対して0.001〜10重量部であることが好
ましく、0.1〜5重量部がさらに好ましい。(D)成
分の量が少なすぎると、組成物の接着性が十分でなく、
多すぎると硬化した接着剤の特性に悪影響を及ぼす。
The blending amount of the component (D) is 100 parts of the component (A).
The amount is preferably 0.001 to 10 parts by weight, more preferably 0.1 to 5 parts by weight, based on parts by weight. If the amount of component (D) is too small, the adhesiveness of the composition will be insufficient and
Too much will adversely affect the properties of the cured adhesive.

【0019】(E)成分の耐熱性付与剤は、過酷な使用
条件のもとにおいても良好な接着機能を維持し、かつ曇
り現象を抑制する、本発明において最も特徴的な成分で
ある。また、シリコーン接着剤を無彩色また微彩色にす
る関係で、色相上の制約をも受ける。このような耐熱性
を付与する機能を有するものとしては、シリコーン接着
剤中のポリシロキサンの酸化や熱分解を抑制する添加剤
が挙げられ、また、充填剤としての機能を兼ねるものが
挙げれる。
The heat resistance imparting agent as the component (E) is the most characteristic component in the present invention, which maintains a good adhesive function even under severe conditions of use and suppresses the fog phenomenon. Further, due to the relationship that the silicone adhesive is achromatic or finely colored, there are restrictions on the hue. Examples of those having the function of imparting such heat resistance include additives that suppress the oxidation and thermal decomposition of polysiloxane in the silicone adhesive, and those that also function as a filler.

【0020】前者の添加剤的な耐熱性付与剤の例として
は、酸化セリウム、水酸化セリウムのような無機セリウ
ム化合物;オクタン酸セリウム、ナフテン酸セリウム、
オクタン酸ランタン、オクタン酸混合希土類金属、オク
タン酸鉄、ナフテン酸鉄のような遷移金属の有機酸塩や
その錯体;セリウム化合物をポリジメチルシロキサンと
加熱して反応させることにより、分子中にセリウム原子
を有するセリウム変性ポリシロキサン;およびMxy
(式中、Mはベリリウム、マグネシウム、カルシウム、
ストロンチルム、バリウム、インジウム、希土類元素、
クロム、モリブデン、タングステンまたは亜鉛を表し;
x,yはそれぞれ金属元素の原子価に応ずる数を表す)
で示される金属酸化物部分を1〜50重量%含有する複
合酸化鉄フェライト(特開昭53−58557号公報)
などが挙げられる。このような添加剤的な耐熱性付与剤
の配合量は、(A)成分100重量部に対して、0.0
01〜10重量部の範囲が好ましい。この範囲を外れる
と、接着剤は十分な耐熱性が得られない。
Examples of the former additive-like heat resistance imparting agent include inorganic cerium compounds such as cerium oxide and cerium hydroxide; cerium octanoate, cerium naphthenate,
Organic acid salts of transition metals such as lanthanum octanoate, mixed rare earth metal octanoate, iron octanoate, and iron naphthenate; and their complexes; Cerium-modified polysiloxane having: and M x O y
(In the formula, M is beryllium, magnesium, calcium,
Strontium, barium, indium, rare earth elements,
Represents chromium, molybdenum, tungsten or zinc;
x and y each represent the number corresponding to the valence of the metal element)
Composite iron oxide ferrite containing 1 to 50% by weight of the metal oxide portion represented by (Japanese Patent Application Laid-Open No. 53-58557).
And so on. The compounding amount of such an additive-like heat resistance imparting agent is 0.0 with respect to 100 parts by weight of the component (A).
A range of 01 to 10 parts by weight is preferable. Outside this range, the adhesive will not have sufficient heat resistance.

【0021】後者の充填剤の機能を兼ねる耐熱性付与剤
の例としては、酸化チタンが挙げられる。この場合、配
合量は、(A)成分100重量部に対して500重量部
以下であり、20〜75重量部が好ましい。この配合量
が多すぎると、脆くなって機械的強度や接着強度を損ね
る。
As an example of the heat resistance-imparting agent having the function of the latter filler, titanium oxide can be mentioned. In this case, the blending amount is 500 parts by weight or less, preferably 20 to 75 parts by weight, based on 100 parts by weight of the component (A). If this blending amount is too large, it becomes brittle and the mechanical strength and adhesive strength are impaired.

【0022】このような耐熱性付与剤のうち、その効果
から、オクタン酸セリウム、オクタン酸鉄および酸化チ
タンが好ましい。酸化チタンは、接着剤に耐熱性を付与
する効果に加えて、ゴム状弾性体としての硬化後の接着
剤に良好な伸びを与えて、ビームランプの点灯、消灯に
伴う温度変化によって接着層に加えられるストレスを吸
収し、接着層の破損を防ぐ効果、ならびにその高い隠蔽
力によって、他の目的で配合した添加剤による多少の彩
色要因を抑制する効果からとくに好ましい。
Of these heat resistance-imparting agents, cerium octanoate, iron octanoate and titanium oxide are preferable in terms of their effects. Titanium oxide, in addition to the effect of giving heat resistance to the adhesive, imparts good elongation to the adhesive after curing as a rubber-like elastic body, so that the adhesive layer can be applied to the adhesive layer due to the temperature change caused by turning on and off the beam lamp. It is particularly preferable because it has an effect of absorbing applied stress to prevent damage to the adhesive layer, and its high hiding power suppresses some coloring factors due to additives added for other purposes.

【0023】このような耐熱性付与剤は、1種を単独で
用いても、2種以上を併用しても差支えない。
Such heat resistance imparting agents may be used alone or in combination of two or more.

【0024】本発明のシリコーン接着剤には、硬化後に
弾性体としての機械的強度を与えるために、充填剤を配
合するのが一般的である。充填剤としては、(E)成分
として示した耐熱性付与剤を兼ねるもののほか、シリコ
ーンゴムの補強性充填剤として一般的に用いられる煙霧
質シリカおよび沈澱シリカ;非補強性充填剤である粉砕
石英、けいそう上、炭酸カルシウム、アルミナ、酸化亜
鉛、カーボンブラックなどが例示される。補強性充填剤
の場合、そのまま用いても、微粉末表面のシラノール基
を環状ポリジメチルシロキサン、ヘキサメチルジシラザ
ンなどと反応させて疎水化したものを用いてもよいが、
このような低分子量の有機ケイ素化合物が接着剤中にそ
のまま残存することは、後述の理由で好ましくない。充
填剤の配合量は、(A)成分100重量部に対して50
0部以下であり、機械的強度や接着強度の点で、5〜2
00重量部が好ましい。
A filler is generally added to the silicone adhesive of the present invention in order to impart mechanical strength as an elastic body after curing. As the filler, in addition to those which also serve as the heat resistance imparting agent shown as the component (E), fumed silica and precipitated silica which are generally used as a reinforcing filler for silicone rubber; ground quartz which is a non-reinforcing filler Examples thereof include calcium carbonate, alumina, zinc oxide, carbon black and the like. In the case of the reinforcing filler, it may be used as it is, or may be one which is hydrophobized by reacting the silanol group on the surface of the fine powder with cyclic polydimethylsiloxane, hexamethyldisilazane, or the like.
It is not preferable that such a low molecular weight organosilicon compound remains in the adhesive as it is for the reason described below. The compounding amount of the filler is 50 with respect to 100 parts by weight of the component (A).
It is 0 part or less, and in terms of mechanical strength and adhesive strength, it is 5 to 2
00 parts by weight is preferred.

【0025】なお、本発明において、ビームランプの接
着剤としてのシリコーン接着剤の機能を向上するため
に、該接着剤に(A)および(B)として配合されるポ
リシロキサン中の低分子シロキサン、たとえばオクタメ
チルシクロテトラシロキサン、デカメチルシクロペンタ
シロキサンなどの含有量を低くすることが好ましい。低
分子シロキサンの含有量は、(A)、(B)両成分の合
計量の1,000ppm 以下であることが好ましく、30
0ppm 以下がさらに好ましい。この低分子シロキサンの
含有量を減らすには、ベースポリマーである(A)成分
中の低分子シロキサン含有量を低くするのが一般的であ
る。このことによって、フロントガラスの曇りを防ぐと
ともに、接着性を向上する効果がある。
In the present invention, in order to improve the function of the silicone adhesive as the adhesive of the beam lamp, the low molecular siloxane in the polysiloxane compounded as (A) and (B) in the adhesive, For example, it is preferable to lower the content of octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane and the like. The content of the low-molecular-weight siloxane is preferably 1,000 ppm or less of the total amount of both components (A) and (B), and 30
It is more preferably 0 ppm or less. In order to reduce the content of the low molecular siloxane, it is general to reduce the content of the low molecular siloxane in the component (A) which is the base polymer. This has the effect of preventing fogging of the windshield and improving the adhesion.

【0026】本発明に用いるシリコーン接着剤は、前述
の各構成成分を所定量配合し、均一に混合することによ
って、硬化して接着剤層を形成することができる。しか
し、(A)〜(C)成分を混合すると常温でも架橋反応
を生じて硬化してしまうので、これらのうち少なくとも
1成分を別にした2包装型として保存し、使用直前に混
合するか、トリアリルイソシアヌレートのような公知の
エチレン系不飽和イソシアヌレートなどの付加反応抑制
剤を配合することにより、1包装型として保存し、使用
に供する。
The silicone adhesive used in the present invention can be hardened to form an adhesive layer by blending a predetermined amount of each of the above-mentioned components and mixing them uniformly. However, when components (A) to (C) are mixed, a crosslinking reaction occurs even at room temperature and the composition hardens. Therefore, at least one of these components is stored in a separate two-pack type and mixed immediately before use, By adding an addition reaction inhibitor such as a known ethylenically unsaturated isocyanurate such as allyl isocyanurate, it is stored as one package and used.

【0027】次に、本発明のビームランプの構造および
製造方法の一例を、図1に示す。
Next, an example of the structure and manufacturing method of the beam lamp of the present invention is shown in FIG.

【0028】まず、ダイクロイックミラー(1)の口金
部(13)に、光源である、たとえばハロゲン電球
(2)の封止部(21)を挿入して、焦点を合わせ、無
機セメント(4)を、口金部(13)から空気が通風し
ないように充填し、加熱して乾燥させる。
First, the sealing portion (21) of a light source, for example, a halogen bulb (2) is inserted into the base portion (13) of the dichroic mirror (1), and the focus is adjusted to the inorganic cement (4). Then, it is filled so that air is not ventilated from the mouthpiece part (13), and heated and dried.

【0029】この光源(2)付ダイクロミックミラー
(1)の端部のフランジ部(11)に未硬化の付加反応
型シリコーン接着剤(5)を塗布し、フロントガラス
(6)をこの部分に載せる。次に、200〜250℃の
高温雰囲気の加熱炉に入れ、この中でミラー(1)とフ
ロントガラス(6)とを組み合わせ、接着剤(5)を硬
化させて、ミラー(1)とフロントガラス(6)を相互
に固着させる。
The uncured addition reaction type silicone adhesive (5) is applied to the flange portion (11) at the end of the dichroic mirror (1) with the light source (2), and the windshield (6) is applied to this portion. Put. Next, the mirror (1) and the windshield (6) are put in a heating furnace in a high temperature atmosphere of 200 to 250 ° C., the adhesive (5) is cured, and the mirror (1) and the windshield are mixed. (6) are fixed to each other.

【0030】このようにして組み合わせた後、フロント
ガラス(6)付ダイクロイックミラー(1)を大気中
(20〜30℃)に取り出し、冷却する。この時、フロ
ントガラス(6)とダイクロミックミラー(1)に囲ま
れた内部の圧力が外気より低下し、外気によりフロント
ガラス(6)とダイクロミックミラー(1)を均一にな
る加圧することになり、接着剤(5)の厚さが均一にな
るように押圧、接着して、フロントガラス付ビームラン
プを得ることができる。
After the above combination, the dichroic mirror (1) with the windshield (6) is taken out into the atmosphere (20 to 30 ° C.) and cooled. At this time, the internal pressure surrounded by the windshield (6) and the dichroic mirror (1) becomes lower than the outside air, and the outside air pressurizes the windshield (6) and the dichroic mirror (1) uniformly. Then, the beam lamp with a windshield can be obtained by pressing and adhering so that the thickness of the adhesive (5) becomes uniform.

【0031】[0031]

【発明の効果】本発明によって、無彩色または微彩色の
付加反応型シリコーン接着剤を使用することにより、広
範囲の使用に対して外観上の問題がなく、またフロント
ガラスとミラーとの間の接着状態がきわめて優れたフロ
ントガラス付ビームランプが得られる。とくに低分子シ
ロキサンの含有量の低い上述の接着剤を用いた場合は、
接着性が優れ、またフロントガラスの曇りを防止するこ
とができる。
According to the present invention, by using an achromatic or light-colored addition reaction type silicone adhesive, there is no appearance problem for a wide range of use, and the adhesion between the windshield and the mirror. A beam lamp with a windshield in excellent condition can be obtained. Especially when the above-mentioned adhesive having a low content of low-molecular-weight siloxane is used,
It has excellent adhesiveness and can prevent fogging of the windshield.

【0032】[0032]

【実施例】以下、本発明を実施例により説明する。な
お、組成物における部は重量部、各測定値は25℃での
値である。本発明はこれらの実施例によって限定される
ものではない。
EXAMPLES The present invention will be described below with reference to examples. In addition, the part in a composition is a weight part and each measured value is a value in 25 degreeC. The invention is not limited by these examples.

【0033】硬化して付加反応型シリコーン接着剤層を
形成するシリコーン組成物として、表1の実施例1〜7
および比較例1〜4の組成物を、各構成成分を均一に混
合することによって調製した。組成物の原料のうち、
(A)〜(D)成分としては表2に示すものを用いた。
Examples 1 to 7 of Table 1 are silicone compositions which cure to form an addition reaction type silicone adhesive layer.
And the compositions of Comparative Examples 1 to 4 were prepared by uniformly mixing the components. Of the ingredients of the composition,
As the components (A) to (D), those shown in Table 2 were used.

【0034】[0034]

【表1】 [Table 1]

【0035】[0035]

【表2】 [Table 2]

【0036】これらの組成物を、図2に示すように、ダ
イクロイックミラーのフランジ部(11)に塗布し、フ
ロントガラス(6)を載せて圧着しつつ、180℃で1
5分間加熱して接着・硬化させることにより、接着剤
(5)層を形成し、光源部分を設けないフロントガラス
付ビームランプの模型を作成して、実用試験に供した。
As shown in FIG. 2, these compositions were applied to the flange portion (11) of the dichroic mirror, and the windshield (6) was placed on the flange portion (1) and pressure-bonded at 180 ° C.
An adhesive (5) layer was formed by heating for 5 minutes for adhesion and curing, and a model of a beam lamp with a windshield having no light source portion was prepared and subjected to a practical test.

【0037】すなわち、この模型を270℃の高温乾燥
器中に配置し、外観(曇り具合)および長期加熱下にお
ける接着性を評価した。接着性の評価の場合、ビームラ
ンプの基部から、矢印の方向に5kgf/cm2 の圧縮空気を
送った。
That is, this model was placed in a high temperature dryer at 270 ° C., and the appearance (cloudiness) and the adhesiveness under long-term heating were evaluated. For the evaluation of adhesiveness, compressed air of 5 kgf / cm 2 was sent from the base of the beam lamp in the direction of the arrow.

【0038】これとは別に、前述の実施例および比較例
の組成物についてせん断接着性の試験を行った。すなわ
ち、JIS K6850の試験法に準じて、ただし1mm
の試料厚さになるように、それぞれの組成物をアルミ板
に塗布し、180℃で15分間加熱して接着・硬化させ
て試片を作成し、せん断接着力を測定した。試験は、常
態、および270℃の恒温乾燥器に100時間放置して
常温に戻したものについて行った。なお、この試料につ
いて、外観を観察した。
Separately, the compositions of the above Examples and Comparative Examples were tested for shear adhesion. That is, according to the JIS K6850 test method, but 1 mm
Each composition was applied to an aluminum plate so as to have a sample thickness of, and heated at 180 ° C. for 15 minutes to be bonded and cured to prepare a test piece, and the shear adhesive strength was measured. The test was performed on the normal state and the one that was left in a constant temperature dryer at 270 ° C. for 100 hours and returned to normal temperature. The appearance of this sample was observed.

【0039】以上の結果を表1に示す。比較例1、2及
び4の接着剤は加熱後のせん断接着性の低下が著しく、
実用試験の結果も、接着剤の耐熱性が悪い。比較例3の
接着剤はそれに比較すると耐熱性が優れているが、外観
が赤褐色であるため、実用上の制約がある。これに対し
て本発明による実施例1〜7の接着剤は、これらのいず
れよりも高い耐熱性を有し、また無色半透明から黒色に
至る無彩色を呈するという利点があることを、表1に示
している。
The above results are shown in Table 1. The adhesives of Comparative Examples 1, 2 and 4 show a remarkable decrease in shear adhesiveness after heating,
The results of the practical tests also show that the heat resistance of the adhesive is poor. The adhesive of Comparative Example 3 is superior in heat resistance to that, but has a practical limitation because it has a reddish brown appearance. On the other hand, the adhesives of Examples 1 to 7 according to the present invention have the advantages that they have higher heat resistance than any of these and exhibit an achromatic color from colorless translucent to black. Is shown in.

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

【図1】本発明の一実施例を示すフロントガラス付ビー
ムランプの構成図である。
FIG. 1 is a configuration diagram of a beam lamp with a windshield showing an embodiment of the present invention.

【図2】接着強度の評価方法を示す図である。なお、左
側(基部を除く)は断面図である。
FIG. 2 is a diagram showing a method for evaluating adhesive strength. The left side (excluding the base) is a sectional view.

【符号の説明】[Explanation of symbols]

1 ダイクロイックミラー 2 電球(例:ハロゲンランプ) 3 端子ピン 4 無機セメント 5 接着剤 6 フロントガラス 11 ダイクロイックミラーのフランジ部 12 レンズ 13 ダイクロイックミラーの口金部 21 電球の封止部 1 Dichroic mirror 2 Light bulb (eg halogen lamp) 3 Terminal pin 4 Inorganic cement 5 Adhesive 6 Windshield 11 Dichroic mirror flange 12 Lens 13 Dichroic mirror base 21 Light bulb sealing

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 耐熱向上剤を含有する無彩色または微彩
色の付加反応型シリコーン接着剤でフロントガラスが接
着されていることを特徴とするビームランプ。
1. A beam lamp, wherein a windshield is adhered with an achromatic or microcolored addition reaction type silicone adhesive containing a heat resistance improver.
JP35130991A 1991-12-13 1991-12-13 Beam lamp with windshield Expired - Fee Related JP3257812B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP35130991A JP3257812B2 (en) 1991-12-13 1991-12-13 Beam lamp with windshield

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP35130991A JP3257812B2 (en) 1991-12-13 1991-12-13 Beam lamp with windshield

Publications (2)

Publication Number Publication Date
JPH05166498A true JPH05166498A (en) 1993-07-02
JP3257812B2 JP3257812B2 (en) 2002-02-18

Family

ID=18416436

Family Applications (1)

Application Number Title Priority Date Filing Date
JP35130991A Expired - Fee Related JP3257812B2 (en) 1991-12-13 1991-12-13 Beam lamp with windshield

Country Status (1)

Country Link
JP (1) JP3257812B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005161132A (en) * 2003-11-28 2005-06-23 Dow Corning Toray Silicone Co Ltd Manufacturing method of silicone laminate
JP2010158897A (en) * 2010-02-09 2010-07-22 Dow Corning Toray Co Ltd Method of manufacturing silicone laminate

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005161132A (en) * 2003-11-28 2005-06-23 Dow Corning Toray Silicone Co Ltd Manufacturing method of silicone laminate
JP4503271B2 (en) * 2003-11-28 2010-07-14 東レ・ダウコーニング株式会社 Method for producing silicone laminate
JP2010158897A (en) * 2010-02-09 2010-07-22 Dow Corning Toray Co Ltd Method of manufacturing silicone laminate

Also Published As

Publication number Publication date
JP3257812B2 (en) 2002-02-18

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