JPH0447658A - Sputter prevented fluorescent lamp - Google Patents
Sputter prevented fluorescent lampInfo
- Publication number
- JPH0447658A JPH0447658A JP15205290A JP15205290A JPH0447658A JP H0447658 A JPH0447658 A JP H0447658A JP 15205290 A JP15205290 A JP 15205290A JP 15205290 A JP15205290 A JP 15205290A JP H0447658 A JPH0447658 A JP H0447658A
- Authority
- JP
- Japan
- Prior art keywords
- lamp
- film
- urethane acrylate
- coating
- fluorescent 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.)
- Pending
Links
- 229920005989 resin Polymers 0.000 claims abstract description 18
- 239000011347 resin Substances 0.000 claims abstract description 18
- 238000000576 coating method Methods 0.000 claims abstract description 15
- 239000011248 coating agent Substances 0.000 claims abstract description 14
- 239000011521 glass Substances 0.000 claims abstract description 14
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000003085 diluting agent Substances 0.000 claims abstract description 5
- 239000008199 coating composition Substances 0.000 claims description 6
- 239000003999 initiator Substances 0.000 claims description 5
- 230000004907 flux Effects 0.000 abstract description 7
- 239000002904 solvent Substances 0.000 abstract description 7
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 238000006243 chemical reaction Methods 0.000 abstract description 2
- 238000001035 drying Methods 0.000 abstract description 2
- 238000006116 polymerization reaction Methods 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000000470 constituent Substances 0.000 abstract 1
- 238000010413 gardening Methods 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 230000003449 preventive effect Effects 0.000 abstract 1
- 230000009257 reactivity Effects 0.000 abstract 1
- 238000001723 curing Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229920001225 polyester resin Polymers 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- -1 amine compound Chemical class 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は新規な飛散防止形蛍光ランプに関するものであ
る。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a novel shatterproof fluorescent lamp.
従来の技術
蛍光ランプはガラスを主要構成材料としており、取扱を
誤って破損した場合、ガラス片が飛び散り、人身事故を
起こすおそれがある。これに対処する方法として、蛍光
ランプのガラス管外面を透明な合成樹脂チューブで覆っ
た飛散防止形蛍光ランプが公知である。これは熱収縮タ
イプのポリエステル樹脂製のチューブをガラス管にかぶ
せ、加熱処理することによりガラス管外面に透明な合成
樹脂製被膜を形成したものである。Conventional fluorescent lamps are mainly composed of glass, and if they are damaged due to improper handling, glass pieces may fly off and cause personal injury. As a method for dealing with this problem, a shatterproof fluorescent lamp is known in which the outer surface of the glass tube of the fluorescent lamp is covered with a transparent synthetic resin tube. This is a tube made of heat-shrinkable polyester resin placed over a glass tube and heated to form a transparent synthetic resin coating on the outer surface of the glass tube.
発明が解決しようとする課題
従来の飛散防止形蛍光ランプには耐候性、膜強度等を考
慮して上記のようなポリエステル樹脂製チューブが用い
られている。しかしながら、このチューブは完全に透明
でないうえに、膜厚が厚いため光束が約3%も低下する
という大きな問題があった。また、チューブがきわめて
高価なうえに、完成したランプにポリエステル樹脂チュ
ーブをかぶせ、加熱炉を通して加熱収縮処理する作業が
必要で、これはきわめて作業性が悪いという問題があっ
た。Problems to be Solved by the Invention Conventional shatterproof fluorescent lamps use polyester resin tubes as described above in consideration of weather resistance, membrane strength, and the like. However, this tube is not completely transparent and has a large film thickness, which causes a major problem in that the luminous flux decreases by about 3%. In addition, the tube is extremely expensive, and it is necessary to cover the completed lamp with a polyester resin tube and heat it in a heating furnace for shrinkage treatment, which is extremely difficult to work with.
本発明は上記従来の問題点を解決するためになされたも
ので、被膜形成が容易で、かつ作業性がよく、光束の低
下を防止した飛散防止形蛍光ランプを提供するものであ
る。The present invention has been made to solve the above-mentioned conventional problems, and provides a shatterproof fluorescent lamp that is easy to form a coating, has good workability, and prevents a decrease in luminous flux.
課題を解決するための手段
この目的を達成するために、本発明の飛散防止形蛍光ラ
ンプはガラス管外面に反応性を有する二重結合を少な(
とも2個含むウレタンアクリレートを主成分とし、これ
に反応性希釈剤、光重合剤および増感剤を加えた塗料用
組成物からなる紫外線硬化樹脂被膜を被着した構成を有
している。Means for Solving the Problems In order to achieve this object, the shatterproof fluorescent lamp of the present invention has fewer reactive double bonds on the outer surface of the glass tube (
It has a structure in which an ultraviolet curable resin film made of a coating composition containing two urethane acrylates as a main component, to which a reactive diluent, a photopolymerizer, and a sensitizer are added is coated.
作用
本発明によると、ガラス管外面に主成分が反応性を有す
る二重結合をもつ官能基を少なくとも2つ有するウレタ
ンアクリレートからなり、これに反応性希釈剤、光重合
開始剤および増感剤からなる塗料用組成物にて紫外線硬
化樹脂被膜を形成するので、従来に比ベガラス管の外面
にきわめて短時間に強靭な被膜を形成することができる
。According to the present invention, the main component on the outer surface of the glass tube is made of urethane acrylate having at least two reactive double bond-containing functional groups, and a reactive diluent, a photopolymerization initiator, and a sensitizer are added to the outer surface of the glass tube. Since the ultraviolet curable resin coating is formed using the coating composition, a tough coating can be formed on the outer surface of the glass tube in a much shorter time than in the past.
実施例
従来技術における飛散防止形蛍光ランプの最も大きな問
題点は被膜形成加工時間が長く、量産性が悪いという点
であった。すなわち、加工時間は代表的な直管40ワッ
ト形蛍光ランプの場合、チューブへのランプの挿入作業
は1本ずつ人手て行う必要があって約2分間要し、さら
に収縮加工時間3分、冷却時間3分、そしてランプ端部
仕上げに約2分間の合計約10分間は必要であった。EXAMPLE The biggest problem with the prior art shatterproof fluorescent lamps is that it takes a long time to form a coating, making it difficult to mass-produce. In other words, in the case of a typical straight tube 40W fluorescent lamp, it takes approximately 2 minutes to manually insert the lamp into the tube one by one, followed by an additional 3 minutes of shrinkage processing and cooling. A total of about 10 minutes was required, including 3 minutes and about 2 minutes to finish the lamp end.
これらの問題を解決し、量産性を高める方法としてラン
プ外面に樹脂膜をコーティング法にて行うことが提案さ
れている。しかしながらこの場合、樹脂の塗布、乾燥に
15分間から20分間必要であり、人手は省けるものの
やはり量産性には大きな問題がある。ところで最近、紫
外線により重合反応を起こし、従来の熱硬化に(らべ硬
化がきわめて迅速に起こる紫外線硬化樹脂が実用化され
ている。この紫外線硬化樹脂の主成分のベースレジンと
しては光重合性のアクリルオリゴマーが用いられる。こ
こでオリゴマーとはモノマーと高分子量のポリマーとの
中間の分子量数千程度のものをいう。発明者は紫外線硬
化樹脂を飛散防止膜へ適用すべく、種々あるアクリルオ
リゴマーについて実験した結果、特に飛散防止膜として
適しているのはウレタンアクリレートであることを見出
した。ウレタンアクリレートは特に飛散防止膜に不可欠
な変色しない強靭な塗膜がきわめて短い硬化時間でえら
れるのが大きな特長である。また、ベースレジンは一般
に粘度が高いために、粘度調整用として紫外線重合性の
低粘度のアクリルモノマーが用いられる。また、紫外線
を吸収してラジカルを生成し、オリゴマーやモノマーに
重合反応を起こさせるための光重合開始剤が添加されて
いる。そして、この光重合開始剤の効果を高めるために
、アミン化合物の増感剤も併せて添加される。本発明に
用いられる紫外線硬化樹脂は作業上の容易性から溶剤と
ともに調合して塗料用組成物として用いられるのが好ま
しい。溶剤にはキシレンのような芳香族炭化水素、酢酸
ブチルのようなエステル類、メチルエチルケトンのよう
なケトン類、ジエチルセルソルブのようなグリコールジ
エーテル類が使用可能である。As a method to solve these problems and improve mass productivity, it has been proposed to coat the outer surface of the lamp with a resin film. However, in this case, it takes 15 to 20 minutes to apply and dry the resin, and although labor can be saved, there is still a big problem in mass production. Recently, ultraviolet curable resins have been put into practical use that cause polymerization reactions with ultraviolet rays, resulting in extremely rapid curing compared to conventional heat curing. Acrylic oligomers are used. Here, oligomers refer to molecules with a molecular weight of several thousand between monomers and high molecular weight polymers. In order to apply ultraviolet curable resins to anti-scattering films, the inventors investigated various acrylic oligomers. As a result of experiments, we found that urethane acrylate is especially suitable as a shatterproof film.Urethane acrylate has the advantage of being able to produce a strong coating film that does not discolor, which is essential for a shatterproof film, in an extremely short curing time. In addition, since base resins generally have a high viscosity, UV-polymerizable, low-viscosity acrylic monomers are used to adjust the viscosity.They also absorb UV rays to generate radicals, which can be polymerized into oligomers and monomers. A photopolymerization initiator is added to cause a reaction.In order to enhance the effect of this photopolymerization initiator, an amine compound sensitizer is also added.Ultraviolet curing used in the present invention For ease of operation, the resin is preferably mixed with a solvent and used as a coating composition.Solvents include aromatic hydrocarbons such as xylene, esters such as butyl acetate, and ketones such as methyl ethyl ketone. , glycol diethers such as diethyl cellosolve can be used.
本発明にかかる塗料用組成物はガラス管外面に塗布され
、その後溶剤を除去するため加熱乾燥したのち、波長3
00〜400ナノメータの近紫外線を数十秒から数分間
というきわめて短時間照射することにより透明な紫外線
硬化樹脂被膜が急速に形成されるのが大きな特長である
。The coating composition according to the present invention is applied to the outer surface of a glass tube, and then heated and dried to remove the solvent.
A major feature is that a transparent ultraviolet curable resin film is rapidly formed by irradiation with near ultraviolet light of 00 to 400 nanometers for an extremely short period of several tens of seconds to several minutes.
次に、本発明の実施例について述べる。Next, examples of the present invention will be described.
反応性を有する二重結合を少なくとも2個含むウレタン
アクリレートを主成分とし、これに反応希釈剤、光重合
開始剤および増感剤を加えた塗料組成物からなる透明な
紫外線硬化樹脂(大日本インキ化学工業株式会社製ユニ
デック・C9−544)を用いて直管20ワット形蛍光
ランプ外面に4g被着する。乾燥は100℃で10分行
い溶剤を除去する。ついで高圧水銀ランプ(出力80
W / cm )から約15cm離れた位置でランプを
回転数5Qrpmで自転させて紫外線をランプ表面の樹
脂膜にまんべんなく照射する。約15秒で硬化が完了す
る。硬化が完了したランプを24時間放置したのち、ラ
ンプを水平に保持して3mの高さから自然落下させる落
下強度試験を行った結果、ランプは破損したものの、ガ
ラス片は被膜に接着して全く飛散しなかった。さらに衝
撃試験において、1mの糸の端に取り付けた200gの
鋼球を30度の角度からランプにあてても、被膜は全く
破れなかった。ついでかかる蛍光ランプの光束を測定し
た結果、被膜を設ける前のランプの光束が1522em
(0時間)であったのに対し、本発明になる飛散防止膜
を形成したものは1520(7mであり、さらに従来の
熱収縮チューブを用いたランプは1462emであり、
本発明の蛍光ランプは被膜による光束低下はほとんどな
く、また従来のものに比べて3%以上も明るがった。さ
らに寿命試験も行ったところ、5ooo時間点灯後にお
いて、本発明の蛍光ランプは従来と同様、黄色に着色す
ることもなく、問題のないことが認められた。A transparent ultraviolet curable resin (Dainippon Ink Co., Ltd.) consisting of a coating composition whose main component is urethane acrylate containing at least two reactive double bonds, to which a reactive diluent, a photopolymerization initiator, and a sensitizer are added. Using Unidec C9-544 (manufactured by Kagaku Kogyo Co., Ltd.), 4 g was applied to the outer surface of a 20-watt straight fluorescent lamp. Drying is performed at 100° C. for 10 minutes to remove the solvent. Next, a high-pressure mercury lamp (output 80
The lamp was rotated at a rotational speed of 5 Qrpm at a position approximately 15 cm away from W/cm2, and the resin film on the lamp surface was evenly irradiated with ultraviolet rays. Curing is completed in about 15 seconds. After the lamp was completely cured, it was left for 24 hours, and then a drop strength test was conducted in which the lamp was held horizontally and allowed to fall naturally from a height of 3 m. Although the lamp was damaged, the glass pieces adhered to the coating and were completely removed. It didn't scatter. Furthermore, in an impact test, the coating did not break at all even when a 200g steel ball attached to the end of a 1m thread was applied to the lamp at an angle of 30 degrees. Then, as a result of measuring the luminous flux of the fluorescent lamp, the luminous flux of the lamp before the coating was applied was 1522 em.
(0 hours), whereas the length of the lamp with the anti-scattering film of the present invention was 1,520 (7 m), and the lamp using the conventional heat shrink tube was 1,462 em.
The fluorescent lamp of the present invention had almost no reduction in luminous flux due to the coating, and was brighter by 3% or more compared to the conventional lamp. Furthermore, when a life test was conducted, it was found that the fluorescent lamp of the present invention did not turn yellow like the conventional fluorescent lamp after being lit for 500 hours, and was found to have no problems.
なお、本発明にかかる紫外線硬化樹脂は上記実施例に示
したものに限定されるものではない。また、溶剤は必ず
しも必要でなく、無溶剤タイプを用いれば溶剤の除去に
要する時間が不要となり、より一層の時間短縮が実現で
きる。Note that the ultraviolet curable resin according to the present invention is not limited to those shown in the above examples. Further, a solvent is not necessarily required, and if a solvent-free type is used, the time required for removing the solvent is not required, and further time reduction can be realized.
発明の詳細
な説明したように、本発明はガラス管外面に反応性を有
する二重結合を少なくとも2個含むウレタンアクリレー
トを主成分とした紫外線硬化樹脂被膜を形成することに
より、光束低下がほとんどなく、かつ従来の熱収縮チュ
ーブを用いたものや、通常の樹脂を用いてランプ外面に
コーティング法にて塗布したものに比べて被膜形成時間
が大幅に短縮でき、量産性を大幅に改善し飛散防止形蛍
光ランプを提供することができるものである。As explained in detail, the present invention has a method of forming an ultraviolet curable resin film mainly composed of urethane acrylate containing at least two reactive double bonds on the outer surface of a glass tube, thereby causing almost no decrease in luminous flux. , and compared to conventional heat-shrink tubes or ordinary resins applied to the outside of the lamp using a coating method, the film formation time can be significantly shortened, greatly improving mass productivity and preventing scattering. It is possible to provide a shaped fluorescent lamp.
Claims (1)
2個含むウレタンアクリレートを主成分とし、このウレ
タンアクリレートに反応性希釈剤、光重合開始剤および
増感剤を加えた塗料用組成物からなる透明な紫外線硬化
樹脂被膜を形成したことを特徴とする飛散防止形蛍光ラ
ンプ。A coating composition consisting of a urethane acrylate containing at least two reactive double bonds on the outer surface of a glass tube as a main component, and a reactive diluent, a photopolymerization initiator, and a sensitizer added to this urethane acrylate. A shatterproof fluorescent lamp characterized by a transparent ultraviolet curing resin coating.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15205290A JPH0447658A (en) | 1990-06-11 | 1990-06-11 | Sputter prevented fluorescent lamp |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15205290A JPH0447658A (en) | 1990-06-11 | 1990-06-11 | Sputter prevented fluorescent lamp |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0447658A true JPH0447658A (en) | 1992-02-17 |
Family
ID=15531998
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15205290A Pending JPH0447658A (en) | 1990-06-11 | 1990-06-11 | Sputter prevented fluorescent lamp |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0447658A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09157581A (en) * | 1995-12-06 | 1997-06-17 | Arakawa Toryo Kogyo Kk | Method for reinforcement of plate glass and coating material for preventing broken glass piece from scattering |
US6409356B1 (en) | 1998-07-01 | 2002-06-25 | Nec Corporation | Liquid crystal display having light-transmitting member in front of light-generating section |
-
1990
- 1990-06-11 JP JP15205290A patent/JPH0447658A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09157581A (en) * | 1995-12-06 | 1997-06-17 | Arakawa Toryo Kogyo Kk | Method for reinforcement of plate glass and coating material for preventing broken glass piece from scattering |
US6409356B1 (en) | 1998-07-01 | 2002-06-25 | Nec Corporation | Liquid crystal display having light-transmitting member in front of light-generating section |
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