JPS5933150B2 - Tube cap adhesive - Google Patents
Tube cap adhesiveInfo
- Publication number
- JPS5933150B2 JPS5933150B2 JP14543476A JP14543476A JPS5933150B2 JP S5933150 B2 JPS5933150 B2 JP S5933150B2 JP 14543476 A JP14543476 A JP 14543476A JP 14543476 A JP14543476 A JP 14543476A JP S5933150 B2 JPS5933150 B2 JP S5933150B2
- Authority
- JP
- Japan
- Prior art keywords
- adhesive
- nozzle
- cap
- application
- phenolic resin
- 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.)
- Expired
Links
- 230000001070 adhesive effect Effects 0.000 title claims description 35
- 239000000853 adhesive Substances 0.000 title claims description 34
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 14
- 239000003960 organic solvent Substances 0.000 claims description 8
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 7
- 239000000843 powder Substances 0.000 claims description 7
- 239000011134 resol-type phenolic resin Substances 0.000 claims description 6
- 239000002245 particle Substances 0.000 claims description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 7
- 239000002904 solvent Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000005011 phenolic resin Substances 0.000 description 5
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 4
- 229920001568 phenolic resin Polymers 0.000 description 4
- 239000000463 material Substances 0.000 description 3
- 229920003986 novolac Polymers 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
- 229940107698 malachite green Drugs 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
【発明の詳細な説明】
この発明は、螢光ランプ、白熱ランプ等の管球への口金
固着に用いられる口金接着剤の改良に関するものである
。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to improvements in cap adhesives used for fixing caps to tubes of fluorescent lamps, incandescent lamps, and the like.
一般に、ガラス部材よりなる管球に、口金キャップを固
着するには、予め口金キャップと管球との接触面に接着
剤を塗布しておき、管球に口金キャップを破せた後、加
熱処理等を行なつて固着している。Generally, in order to fix a cap to a tube made of a glass material, adhesive is applied to the contact surface between the cap and the tube in advance, and after the cap is broken onto the tube, heat treatment is applied. etc., and it is fixed.
そして、この口金キヤツプヘの接着剤の塗布は、図に示
すように接着剤を加圧しつつ蓄えたタンク1と弁2を持
つノズル3を用い、口金キャップ4をノズル3に対して
所定の間隙をもつて嵌合するよう配置して行なわれる。
つまり、図示の状態で一定時間弁2を開けば、接着剤5
がノズル3からリング状にはみ出し、所定量口金キャッ
プ4の内周面に塗布される。そして、弁2を閉じて、口
金キャップ4をノズル3位置から取りはづせば、口金キ
ャップ4の所定位置に接着剤5が塗布される。そして、
この工程で問題とされていたのは、接着剤が軟かすぎた
り、粘性が大きいことによる接着剤5のノズル3からの
切れの悪さである。Then, as shown in the figure, the adhesive is applied to the nozzle cap using a nozzle 3 with a tank 1 and a valve 2 that hold the adhesive under pressure while keeping a predetermined gap between the nozzle cap 4 and the nozzle 3. This is done by arranging them so that they fit together.
In other words, if the valve 2 is opened for a certain period of time in the state shown, the adhesive 5
protrudes from the nozzle 3 in a ring shape and is applied to the inner peripheral surface of the mouthpiece cap 4 in a predetermined amount. Then, when the valve 2 is closed and the nozzle cap 4 is removed from the nozzle 3 position, the adhesive 5 is applied to a predetermined position of the nozzle cap 4. and,
The problem in this process is that the adhesive 5 is not easily cut from the nozzle 3 due to the adhesive being too soft or having high viscosity.
即ち、切れが悪いと、弁2を閉じ、ノズル3から口金キ
ャップ4をはずした時に、ノズルロ周辺に、接着剤が残
つて盛り上がつたり、たれ下がつたりして、塗布形状が
くずれると共に塗布される量が不均一になつて種々のト
ラブルを発生し、甚しい場合はノズルロにたまつた接着
剤によつて塗布作業ができなくなることもある。更に、
要求されている性能としては、塗布後の保管に適するよ
う形くずれしない適当な固さと接着剤の性質が一定期間
保たれることである。In other words, if the adhesive is poorly cut, when the valve 2 is closed and the nozzle cap 4 is removed from the nozzle 3, adhesive remains around the nozzle nozzle and swells or drips, causing the applied shape to be distorted. At the same time, the amount of adhesive applied becomes uneven, causing various problems, and in severe cases, the adhesive accumulated in the nozzle tube may make it impossible to perform the application process. Furthermore,
The required performance is that the adhesive maintains its proper hardness and adhesive properties for a certain period of time so that it does not lose its shape and is suitable for storage after application.
即ち、管球への口金キャップの固着に比べて、接着剤の
塗布工程のピッチは早いので、接着剤を塗布したキャッ
プを作りだめすることが、作業の効率を高めるために行
なわれる。そして、一定期間容器に入れられて保管され
るのであるが、この場合、容器内で、口金キャップ同志
がランダムな向きで蝕れ合うので、接着剤が軟いと塗布
された接着剤が他の口金キャップのピン等に付着して外
観特性が低下したり、ランプとしての接続不良の原因と
なる。ところで、従来、この接着剤はロジン、セラミッ
クなどの天然樹脂、及びフェノール樹脂、炭酸・、カル
シウムの微粉末、マラカイトグリーン、シリーコン樹脂
等の材料を溶剤に溶かして得られ、溶剤としてエタノー
ル等の有機溶剤を用いるタイプと、トリオキサンを用い
るタイプがある。That is, since the pitch of the adhesive application process is faster than that of fixing the base cap to the tube, it is necessary to prepare the caps coated with adhesive in order to improve work efficiency. Then, they are stored in a container for a certain period of time, but in this case, the caps of the caps corrode each other in random directions within the container, so if the adhesive is soft, the applied adhesive will rub off on other caps. It adheres to the pins of the cap, etc., deteriorating the appearance characteristics and causing poor connection as a lamp. By the way, conventionally, this adhesive is obtained by dissolving materials such as natural resins such as rosin and ceramics, phenolic resin, carbonate/calcium fine powder, malachite green, and silicone resin in a solvent, and organic resins such as ethanol are used as the solvent. There are two types: one using a solvent and the other using trioxane.
そして、塗布後の保管に適した性能から比較すると、有
機溶剤を用いたものは、安価ではあるが塗布後も軟くて
、保存期間も3日程度と短く、トリオキサンを使用した
ものは高価ではあるが塗布後は固化し、保存期間は3ケ
月以上と長いという差異があつた。即ち、有機溶剤を用
いたものは、材料の混合から塗布作業までを全て常温に
て行ない。加熱による固着前には、有機溶剤によつて可
塑性を保つているので、塗布後も塗布時と同じ軟い状態
を保つのである。そして、その保存期間は溶剤の蒸発量
の少ない期間に制限され、3日間と短いわけである。そ
して、一方トリオキサンを溶剤として使用したものは、
常温で固化し、予熱すると軟化する性質を持つので、混
合及び塗布等の軟化が必要な時のみ500C〜60℃に
予熱している。Comparing properties suitable for storage after application, those using organic solvents are inexpensive but remain soft after application and have a short shelf life of about 3 days, while those using trioxane are not expensive. However, the difference was that it solidified after application and had a long storage period of over three months. That is, in the case of using an organic solvent, the entire process from mixing the materials to coating is performed at room temperature. Since the plasticity is maintained by the organic solvent before it is fixed by heating, it maintains the same soft state after application as it was at the time of application. The storage period is limited to a period during which the amount of solvent evaporation is small, and is as short as three days. On the other hand, those using trioxane as a solvent,
Since it has the property of solidifying at room temperature and softening when preheated, it is preheated to 500C to 60C only when softening is necessary for mixing, coating, etc.
このため、塗布後には常温におけば固化し、しかも溶剤
が蒸発しにくい状態となり、保管に適した性能を与える
わけである。そこで、この発明は上記事情に鑑み、これ
を改良したもので、粘性が小さくてノズルからの切れが
よく、しかも塗布後に適当な固さを持つと共にその保存
期間が長い接着剤を安価に提供する。For this reason, after application, it solidifies at room temperature and is in a state where the solvent is difficult to evaporate, giving it performance suitable for storage. Therefore, in view of the above circumstances, this invention is an improvement on the above, and provides an inexpensive adhesive that has low viscosity, can be easily cut from a nozzle, has appropriate hardness after application, and has a long shelf life. .
即ち、この発明の接着剤は、安価に生産するために、溶
剤としては、エタノール等の有機溶剤を用いるものであ
るが、切れをよくするために、70μ以下の炭酸カルシ
ウムの微粉末が10%〜50重量%の範囲のものを使用
し、更に保存性能を向上させるために、成分中のフエノ
ール樹脂として、従来のノボラツクタイプのものに代え
てレゾールタイプのものを使用し、従来の有機溶剤を用
いた接着剤に比べて固く練りあげて使用するものである
。なお、ここでノボラツクタイプのフエノール樹脂とは
、ホルムアルデヒドに対しフエノールを過剰にして酸性
触媒下で反応させた樹脂であつて、ホルムアルデヒドを
発生する物質(ヘキサメチルテトラシン)を加えて加熱
すると硬化するものである。That is, the adhesive of the present invention uses an organic solvent such as ethanol as a solvent in order to produce it at a low cost, but in order to make it cut easily, it contains 10% calcium carbonate fine powder of 70μ or less. ~50% by weight, and in order to further improve storage performance, a resol type phenolic resin was used instead of the conventional novolak type as the phenol resin in the ingredients, and a resol type was used instead of the conventional novolac type. It is used by kneading it harder than adhesives that use . Note that novolak type phenolic resin is a resin made by reacting an excess of phenol with respect to formaldehyde under an acidic catalyst, and it hardens when heated with the addition of a substance that generates formaldehyde (hexamethyltetracine). It is something to do.
また、レゾールタイプのフエノール樹脂とは、フエノー
ルに対しホルムアルデヒドを過剰にしてアルカリ性触媒
下で反応させた樹脂で加熱すると硬化するものである。
そして、このレゾールタイプのフエノール樹脂を用いた
のは、トリオキサンを使用した接着剤のように、塗布時
にのみ予熱して軟化させ、塗布後の保管時には常温の固
い状態におくという扱いを可能にするためのものである
。Furthermore, resol type phenolic resin is a resin made by reacting an excess of formaldehyde with respect to phenol under an alkaline catalyst, and is cured when heated.
The use of this resol-type phenolic resin allows it to be treated like adhesives using trioxane, where it is softened by preheating only during application, and then left in a hard state at room temperature when stored after application. It is for.
即ち、有機溶剤により固く練りあげた接着剤を、塗布時
のみ50℃〜60℃で予熱して軟化させて使用するが、
従来のようにノボラツクタィプのフエノール樹脂を使用
すると、2時間程で完全に硬化してしまい接着剤として
の機能を失うので、このような取り扱いが出来ないので
ある。ところが、この発明のようにレゾールタイプのフ
エノール樹脂を使用したものでは、15時間加熱しても
可塑性を保持するので、高価なトリオキサンを使用した
接着剤と同様な取り扱いが可能で、口金キヤツプへの塗
布後も約7日間(アルコール蒸気中で保存すれば約3ケ
月)の保存が可能であり、この点からも、保存性がよく
なる。なお、70μ以下の粒度範囲の炭酸カルシウムが
50%を越えた場合は、接着剤の粘性が大きく、10%
未満の場合は逆に粘性が小さすぎで、いずれの場合も接
着剤の口金キヤツプへの効果的な塗布ができない。That is, the adhesive is hardened with an organic solvent and is softened by preheating at 50°C to 60°C only during application.
If a novolatile type phenolic resin is used as in the past, it will completely harden in about two hours and lose its function as an adhesive, so it cannot be handled in this way. However, products using resol type phenolic resin as in this invention retain their plasticity even after being heated for 15 hours, so they can be handled in the same way as adhesives using expensive trioxane, and they do not attach to the base cap. After application, it can be stored for about 7 days (about 3 months if stored in alcohol vapor), and from this point of view as well, it has good shelf life. In addition, if calcium carbonate in the particle size range of 70μ or less exceeds 50%, the viscosity of the adhesive becomes large and 10%
On the other hand, if it is less than that, the viscosity is too low, and in either case, the adhesive cannot be effectively applied to the base cap.
要するに、この発明では70μ以下の炭酸カルシウム微
粉末の粒度範囲を10%〜50重量%と制限したことに
より、ノズルからの切れをよくし、レゾールタイプのフ
エノール樹脂を用いたことによつて、安価な有機溶剤を
用いた接着剤であつても、塗布時にのみ予熱して、軟化
させ、常温では保存に適した固さにすることを可能とし
たものである。In short, in this invention, by limiting the particle size range of the calcium carbonate fine powder of 70μ or less to 10% to 50% by weight, it can be easily cut from the nozzle, and by using a resol type phenolic resin, it is inexpensive. Even if the adhesive uses an organic solvent, it can be preheated only at the time of application to soften it and make it hard enough to be stored at room temperature.
以上説明したように、本発明はレゾールタイフのフエノ
ール樹脂と炭酸カルシウムの微粉末を主成分とし、有機
溶剤で溶解されたものにおいて、上記炭酸カルシウムの
微粉末における70μ以下の粒度範囲を10〜50重量
%とした管球用口金接着剤を提供したがら、ノズルから
の切れがよくなつて口金キヤツプへの塗布作業が円滑に
行なえ作業性が向上する。As explained above, the present invention is mainly composed of Resoltaif phenolic resin and fine powder of calcium carbonate, and in a product dissolved in an organic solvent, the particle size range of 70μ or less in the fine powder of calcium carbonate is 10 to 50% by weight. %, the adhesive for tube caps can be easily cut from the nozzle, and the application work to the cap cap can be performed smoothly, improving work efficiency.
また、高価なトリオキサンを使用しなくても、トリオキ
サンを用いたのと同様な効果をあげることができ、塗布
後ランダムに積みあげても他の口金キヤツプ、ピンへの
付着や型くずれ等によるトラブルを生じないので安価な
接着剤での作りだめを可能にした。In addition, it is possible to achieve the same effect as using trioxane without using expensive trioxane, and even if it is piled up randomly after application, it will not cause problems such as adhesion to other caps and pins or deformation. Since it does not occur, it is possible to make it with an inexpensive adhesive.
図は口金キヤツプへの管球用接着剤の塗布方法の説明図
である。
4・・・・・・口金キャツプ、5・・・・・・接着剤。The figure is an explanatory diagram of a method of applying tube adhesive to the base cap. 4...Base cap, 5...Adhesive.
Claims (1)
の微粉末を主成分とし、有機溶剤で溶解されたものにお
いて、上記炭酸カルシウムの微粉末における70μ以下
の粒度範囲を10〜50重量%としたことを特徴とする
管球用口金接着剤。1 The main components are a resol type phenolic resin and a fine powder of calcium carbonate, which is dissolved in an organic solvent, and is characterized in that the fine powder of calcium carbonate has a particle size range of 70μ or less at 10 to 50% by weight. Tube cap adhesive.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14543476A JPS5933150B2 (en) | 1976-12-02 | 1976-12-02 | Tube cap adhesive |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14543476A JPS5933150B2 (en) | 1976-12-02 | 1976-12-02 | Tube cap adhesive |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5369234A JPS5369234A (en) | 1978-06-20 |
| JPS5933150B2 true JPS5933150B2 (en) | 1984-08-14 |
Family
ID=15385146
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14543476A Expired JPS5933150B2 (en) | 1976-12-02 | 1976-12-02 | Tube cap adhesive |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5933150B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59213784A (en) * | 1983-05-18 | 1984-12-03 | Matsushita Electronics Corp | Adhesive for base of electric bulb |
-
1976
- 1976-12-02 JP JP14543476A patent/JPS5933150B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5369234A (en) | 1978-06-20 |
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