JPS5975967A - Fluorescent color ink for writing utensil - Google Patents

Fluorescent color ink for writing utensil

Info

Publication number
JPS5975967A
JPS5975967A JP18658982A JP18658982A JPS5975967A JP S5975967 A JPS5975967 A JP S5975967A JP 18658982 A JP18658982 A JP 18658982A JP 18658982 A JP18658982 A JP 18658982A JP S5975967 A JPS5975967 A JP S5975967A
Authority
JP
Japan
Prior art keywords
ink
copper
fluorescent
gelation
orange
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP18658982A
Other languages
Japanese (ja)
Inventor
Hiromi Sano
博美 佐野
Hidetoshi Hamamoto
浜本 秀俊
Osamu Nishiwaki
西脇 理
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.)
Pentel Co Ltd
Original Assignee
Pentel 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 Pentel Co Ltd filed Critical Pentel Co Ltd
Priority to JP18658982A priority Critical patent/JPS5975967A/en
Publication of JPS5975967A publication Critical patent/JPS5975967A/en
Pending legal-status Critical Current

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  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

PURPOSE:To provide the titled ink free from gelation and reactivity to copper metals, by incorporating aliphatic amides in a fluorescent pigment. CONSTITUTION:A fluorescent color ink for writing utensils which comprises fluorescent pigments [e.g.; Shinroihi Color FM11 (red-orange), 12 (green), or 13 (red)], aliphatic amides (e.g., Armide 18), resins (e.g., phenolic resin), and org. solvents (e.g., xylene) at the least. So far, when oily fluorescent color inks were charged in writing utensils in which copper or copper-contg. metal parts are used fluorescent pigments in the ink were apt to react with copper with the lapse of time to cause gelation of inks. By incorporating aliphatic amides, prevention of the gelation and excellent prolonged stability are achieved.

Description

【発明の詳細な説明】 本発明は筆記具用螢光色インキに関し、更に詳しくは銅
、又は銅を含む金属に対して反応性を有しなり筆記具用
螢光色インキに関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a fluorescent ink for writing instruments, and more particularly to a fluorescent ink for writing instruments that is reactive with copper or metals containing copper.

近年、螢光顔料を有機溶剤に分散させた油性の螢光色イ
ンキを充填した筆記具がその耐水性の点、又多ぐの被筆
記体に筆記できるなどの利点よシ注目されている。又、
上記インキに酸化チタンを添加したインキを充填した筆
記具が上記利点に隠蔽性を加えた点でより注目されてい
る。一方、上記筆記具に使用する金属部材の材質として
、その加工性、コストの点から銅、又は洋白、真鍮など
銅を含有する金属が使用されてきて因る。しかしながら
前記した油性の螢光色インキを上記した銅、又は銅を含
む金属部材を使用した筆記具に充填した場合、経時的に
インキ中の螢・光顔料が銅と反応し、インキがゲル化し
てしまうといった問題を有していた。
In recent years, writing instruments filled with an oil-based fluorescent ink in which fluorescent pigments are dispersed in an organic solvent have attracted attention because of their water resistance and the ability to write on a wide variety of objects. or,
A writing instrument filled with an ink obtained by adding titanium oxide to the above-mentioned ink is attracting more attention because it has added concealability to the above-mentioned advantages. On the other hand, copper, or metals containing copper such as nickel silver and brass have been used as the material for the metal members used in the above-mentioned writing implements from the viewpoint of workability and cost. However, when the above-mentioned oil-based fluorescent ink is filled into a writing instrument that uses the above-mentioned copper or a metal member containing copper, the firefly/light pigment in the ink reacts with the copper over time, causing the ink to gel. It had problems such as storage.

本発明者らは上記問題を解決するために鋭意研究を重ね
た結果、前記した油性の螢光色インキに脂肪族アマイド
を添加することによって銅と螢光顔料との反応性が著し
く低下することを見い出し1本発明を完成したものであ
る。即ち。
The present inventors have conducted extensive research to solve the above problem, and have found that by adding an aliphatic amide to the oil-based fluorescent ink described above, the reactivity between copper and the fluorescent pigment is significantly reduced. Heading 1 completes the present invention. That is.

本発明は銅、又は銅を含む金属部材を使用した筆記具に
おいて、螢光顔料と脂肪族アマイドと樹脂と有機溶剤と
から少なくともなる筆記具用螢光色インキを要旨とする
ものである。
The gist of the present invention is a fluorescent ink for a writing instrument using copper or a metal member containing copper, which comprises at least a fluorescent pigment, an aliphatic amide, a resin, and an organic solvent.

本発明の筆記具用螢光色インキが何故、銅との反応によ
るゲル化を極力防止するのかは定かではないが以下のよ
うに推察する。
It is not clear why the fluorescent ink for writing instruments of the present invention prevents gelation due to reaction with copper as much as possible, but it is speculated as follows.

インキがゲル化する要因として考えられることは、イン
キ中に遊離した銅イオンと螢光顔料の主成分である塩基
性染料とが何らかの反応をしインキをゲル化させるもの
と思われ1本発明に使用の脂肪族アマイドが遊離した銅
イオンと何らかの反応を起こし、銅イオンが塩基性染料
と反応するのを防止するか、もしくは銅のイオン化を極
力防止する何らかの働きを有しているものと思われる。
A possible cause of the gelation of the ink is that the copper ions liberated in the ink and the basic dye, which is the main component of the fluorescent pigment, react in some way, causing the ink to gel. It is thought that the aliphatic amide used causes some kind of reaction with the liberated copper ions, and either prevents the copper ions from reacting with the basic dye, or has some kind of function to prevent copper ionization as much as possible. .

以下1本発明の各成分について詳細に説明する。螢光顔
料は筆跡に鮮やかな色調を与えるために使用するもので
、その具体例を挙げればシンロイヒカ−5−FM11(
レッドオレンジ)。
Each component of the present invention will be explained in detail below. Fluorescent pigments are used to give vivid color tones to handwriting, and a specific example is Shinroi Hika-5-FM11 (
red orange).

同12(グリーン)、同13(レッド)、同14(オレ
ンジ)、M2S(レモンイエロー)、同16(オレンジ
イエローフ、同17(ピンク)。
12 (green), 13 (red), 14 (orange), M2S (lemon yellow), 16 (orange yellow), 17 (pink).

同18(ブルー)、同25(グリニッシニイエU−)、
同27(マゼンダ)、同1o3(レッドノ。
Same 18 (Blue), Same 25 (Grinissinie U-),
Same 27 (Magenta), Same 1o3 (Red No.

同104 (オレンジ)、同105(レモンイエロー)
、同106(オレンジイエロー)、同107(ピンク)
、同108(スカイブルー)(以上。
104 (orange), 105 (lemon yellow)
, 106 (orange yellow), 107 (pink)
, 108 (sky blue) (and above).

シンロイヒ■製)、MPI50(赤橙色)、同501(
緑色)、同5o3(赤)、同5o4(オレンジ)、同5
o5(黄色)、同5o6(黄橙色)。
made by Shinroihi ■), MPI50 (red-orange), MPI501 (made by
green), 5o3 (red), 5o4 (orange), 5o
o5 (yellow), 5o6 (yellow-orange).

同507(ピンク)、同508(青)、同5070(ピ
ンク)(以上1日本螢光化学■製)などがあり、これら
を単独もしくは複数混合して使用でき。
There are 507 (pink), 508 (blue), and 5070 (pink) (manufactured by Nippon Hyouko Kagaku ■), and these can be used alone or in combination.

その使用量はインキ全量に対して1〜50重量%が好ま
しく1色調、粘度の点から5〜40重景%がよシ好まし
い。
The amount used is preferably 1 to 50% by weight based on the total amount of ink, and from the viewpoint of one color tone and viscosity, 5 to 40% by weight is more preferable.

脂肪族アマイドは螢光顔料と銅との反応性を低下させ、
その結果インキのゲル化を極力防止する目的で使用する
ものであり、その具体例を挙げると、アーマイド18.
同HT、同C1同0.アーモワックスEBS(以上、 
 ライオン・アーマ−■製)、キレスライドC(キレス
ト化学■製)などがあり、その使用量はインキ全量に対
して0.01〜5.0重量%が好ましく、0.011重
量%り少な−と効果が弱く5.0重量%より多くてもも
はや仁れ以上の効果は認められずコスト的に不利である
Aliphatic amide reduces the reactivity of fluorescent pigments with copper,
As a result, it is used for the purpose of preventing gelation of ink as much as possible, and a specific example is Aramide 18.
Same HT, Same C1 Same 0. Armowax EBS (and above)
Lion Armor (manufactured by ■), Killeslide C (manufactured by Killest Chemical ■), etc., and the amount used is preferably 0.01 to 5.0% by weight based on the total amount of ink, and less than 0.011% by weight. The effect is weak, and even if the amount is more than 5.0% by weight, no effect beyond that of keratosis can be observed, which is disadvantageous in terms of cost.

樹脂は筆跡の定着性を向上させるため、及びインキの粘
度を調節するために使用するものであり、油溶性のもの
であれば各種使用可能であるが、その−例を挙げると、
ガムロジン、マレイン酸樹脂、アルキッド樹脂、フェノ
ール樹脂。
The resin is used to improve the fixation of handwriting and to adjust the viscosity of the ink, and various oil-soluble resins can be used; examples include:
Gum rosin, maleic acid resin, alkyd resin, phenolic resin.

ケトン樹脂、アクリル樹脂、テルペン樹脂、芳香族炭化
水素系樹脂などがあり、これらを単独もしくは複数混合
して使用でき、その使用量は樹脂の種類9重合度などに
より異なるが、インキ全量に対して1〜50重量%が好
ましい。1重i%より少ないと、筆跡の被筆記面への定
着性が充分でなく、50重量%より多いとインキの粘度
が高くなり、筆跡のかすれ、ペン先の目詰りなどを生じ
やすくなる。
There are ketone resins, acrylic resins, terpene resins, aromatic hydrocarbon resins, etc., and these can be used alone or in combination.The amount used varies depending on the type of resin 9 degree of polymerization, etc., but it is based on the total amount of ink. 1 to 50% by weight is preferred. If it is less than 1% by weight, the fixation of handwriting on the surface to be written will not be sufficient, and if it is more than 50% by weight, the viscosity of the ink will become high, which tends to cause blurred handwriting, clogging of the pen tip, etc.

5− 有機溶剤は被筆記面の使用材質並びに使用される他の素
材により適宜選択できるが、その−例を挙げると、メチ
ルアルコール、エチルアルコール、イソプロピルアルコ
ール+n−ブチルアルコールなどのアルコール系溶剤、
  メチルセロソルブ、エチルセロソルブ、インプロピ
ルセロソルブ、ブチルセロソルブなどのグリコールエー
テル系溶剤、酢酸エチル、酢酸ブチル、酢酸アミルなど
のエステル系溶剤、トルエン、キシレンなどの芳香族系
溶剤などがあり、これらの単独もしくは複数混合して使
用でき、その使用量はインキ全量に対して50〜90重
量%が好まし騒。
5- The organic solvent can be selected as appropriate depending on the material used for the writing surface and other materials used, but examples include alcoholic solvents such as methyl alcohol, ethyl alcohol, isopropyl alcohol + n-butyl alcohol,
These include glycol ether solvents such as methyl cellosolve, ethyl cellosolve, inpropyl cellosolve, and butyl cellosolve, ester solvents such as ethyl acetate, butyl acetate, and amyl acetate, and aromatic solvents such as toluene and xylene. They can be used in combination, and the amount used is preferably 50 to 90% by weight based on the total amount of ink.

上記成分以外に必要に応じて筆跡の隠蔽力をあげる目的
で酸化チタンなどの白色顔料を適宜添加することもでき
、その他界面活性剤、防錆剤、補色用染料などを適宜使
用することも可能である。
In addition to the above ingredients, white pigments such as titanium oxide can be added as necessary to increase the hiding power of handwriting, and other surfactants, rust preventives, complementary color dyes, etc. can also be used as appropriate. It is.

次に本発明のインキの製造方法を簡単に述べ6一 る。Next, the method for manufacturing the ink of the present invention will be briefly described6-1. Ru.

前記成分を必要量混合しく必要に応じて、酸化チタンや
、他の添加剤をも混合し)、ボールミルなどの分散機で
充分攪拌し9分散させることにより容易に本発明のイン
キを得ることができる。
The ink of the present invention can be easily obtained by mixing the above-mentioned components in the required amounts (adding titanium oxide and other additives as necessary), stirring thoroughly with a dispersion machine such as a ball mill, and dispersing the mixture. can.

以下、実施例により1本発明をより詳細に説明する。実
施例中「部」とあるのは「重量部」を示す。
Hereinafter, the present invention will be explained in more detail with reference to Examples. In the examples, "parts" indicate "parts by weight."

実施例 1 ンンロイヒカラ−FM17(ピンク色1顔料。Example 1 Nunroihikara-FM17 (Pink 1 pigment.

シンロイヒ(株制)               1
60部キレスライドC(脂肪族アマイド。
Shinroihi (stock system) 1
60 parts Killeslide C (aliphatic amide).

キレスト化学(作製)               
05部ベツコソール1308(アルキッド樹脂。
Chrest Chemical (Preparation)
05 parts Betsukosol 1308 (alkyd resin.

大口インキ化学工業(株制)2.Q部 ニトロセルロース′/8(セルロース9導体。Oguchi Ink Chemical Industry Co., Ltd. 2. Q section Nitrocellulose'/8 (Cellulose 9 conductor.

HER,0ULES  IN 0ORPORATED製
)   30部酢酸ブチル            5
8.0部キンレン             10.0
部酸化チタンA−220(アナターゼ型酸化チタン。
HER, 0ULES IN 0ORPORATED) 30 parts Butyl acetate 5
8.0 parts Kinren 10.0
Titanium oxide A-220 (anatase type titanium oxide.

石原産業(作製)                 
11.0部上記成分を小型実験用ボールミルに入れ常温
にて72時間攪拌し1分散させることにより。
Ishihara Sangyo (production)
11.0 parts The above ingredients were placed in a small experimental ball mill and stirred at room temperature for 72 hours to disperse.

ピンク色の螢光色インキを得た。A pink fluorescent ink was obtained.

比較例 1 実施例1の成分中キレスライドOを除いた他は実施例1
と同様にしてピンク色の螢光色インキを得た。
Comparative Example 1 Same as Example 1 except that Killeslide O was excluded from the ingredients in Example 1.
In the same manner as above, a pink fluorescent ink was obtained.

比較例 2 実施例1の成分中、キレスライドCを除き。Comparative example 2 Among the components of Example 1, Killeslide C was excluded.

その分だけ13 T L (ベンゾトリアゾール、防錆
剤)を加えた以外は実施例1と同様処してピンク色の螢
光色インキを得た。
A pink fluorescent ink was obtained in the same manner as in Example 1, except that 13TL (benzotriazole, rust preventive) was added accordingly.

実施例 2 MPI304(オレンジ色螢光顔料。Example 2 MPI304 (orange fluorescent pigment.

日本螢光化学(作製)              1
60部アーマイ ド(脂肪族アマイド。
Nippon Fluorochemicals (preparation) 1
60 parts aamide (aliphatic amide).

ライオン・アーマ−(株制)1.0部 マルキード會2(マレインiH1脂)      q、
 o 部メチルイソブチルケトン      200部
n−プロピルアルコール      160部キンレン
             200部酸化チタンR・8
20 H(ルチル型酸化チタン。
Lion Armor Co., Ltd. 1.0 part Malkidokai 2 (Malein iH1 fat) q,
o part Methyl isobutyl ketone 200 parts n-propyl alcohol 160 parts Kinren 200 parts Titanium oxide R.8
20H (Rutile type titanium oxide.

石原産業(作製)                 
21.0部上記成分を小型実験用ボールミルに入れ常温
にて72時間攪拌し分散させることKよシ、オレンジ色
の螢光色インキを得た。
Ishihara Sangyo (production)
21.0 parts The above ingredients were placed in a small experimental ball mill and stirred and dispersed at room temperature for 72 hours to obtain an orange fluorescent ink.

比較例 3 実施例2の成分中、アーマイド18を除いた他は実施例
2と同様にしてオレンジ色の螢光色インキを得た。
Comparative Example 3 An orange fluorescent ink was obtained in the same manner as in Example 2, except that Aamide 18 was removed from the ingredients in Example 2.

比較例 4 実施例2の成分中、アーマイド18を除き。Comparative example 4 Among the components of Example 2, Aamide 18 was excluded.

その分だけBTLを加えた以外は実施例2と同様にして
オレンジ色の螢光色インキを得た。
An orange fluorescent ink was obtained in the same manner as in Example 2, except that BTL was added accordingly.

9− 以上、実施例1,2.比較例1〜4で得られたインキに
ついて金属部月との反応性試験の結果を表−1に示す。
9- Above, Examples 1 and 2. Table 1 shows the results of the reactivity test with metal parts for the inks obtained in Comparative Examples 1 to 4.

表  −1 ※1. 金属部材との反応性試験 実施例1.2.比較例1〜4で得られたインキ10gを
栓付試験管に充填したものを。
Table-1 *1. Reactivity test example 1.2 with metal members. A test tube with a stopper was filled with 10 g of the ink obtained in Comparative Examples 1 to 4.

3本づつ計18本作成し、各々に銅、洋白。A total of 18 pieces were made, 3 pieces each, each made of copper and nickel silver.

真鍮の金属部材(径5 M 、高さ15鵡の円筒形のも
の)を入れ、70℃恒温槽中に7日間10− 放置し、78後インキの状態を目視にて観察し、経時前
と変化のないものを○、経時前に比べてやや変化がみら
れるものを△、インキがゲル化し、完全に変色している
ものを×とした。
A brass metal member (a cylindrical piece with a diameter of 5 M and a height of 15 mm) was placed and left in a constant temperature bath at 70°C for 7 days. After 78 days, the state of the ink was visually observed, and it was compared with before and after aging. An item with no change was rated as ○, an item with a slight change compared to before aging was rated as △, and an item where the ink had gelled and completely changed color was rated as ×.

以上のように本発明の筆記具用螢光色インキは、銅、又
は銅を含む金属部材の筆記具に充填しても、経時的にイ
ンキのゲル化を生じない。
As described above, even when the fluorescent ink for writing instruments of the present invention is filled into a writing instrument made of copper or a metal member containing copper, the ink does not gel over time.

経時安定性に優れたものである。It has excellent stability over time.

特許出願人 ぺんてる株式会社 11−Patent applicant: Pentel Co., Ltd. 11-

Claims (1)

【特許請求の範囲】[Claims] 銅、又は銅を含む金属部材を使用した筆記具において、
螢光顔料と脂肪族アマイドと樹脂と有機溶剤とから少な
くともなる筆記具用螢光色インキ。
In a writing instrument using copper or a metal member containing copper,
A fluorescent ink for writing instruments comprising at least a fluorescent pigment, an aliphatic amide, a resin, and an organic solvent.
JP18658982A 1982-10-22 1982-10-22 Fluorescent color ink for writing utensil Pending JPS5975967A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18658982A JPS5975967A (en) 1982-10-22 1982-10-22 Fluorescent color ink for writing utensil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18658982A JPS5975967A (en) 1982-10-22 1982-10-22 Fluorescent color ink for writing utensil

Publications (1)

Publication Number Publication Date
JPS5975967A true JPS5975967A (en) 1984-04-28

Family

ID=16191189

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18658982A Pending JPS5975967A (en) 1982-10-22 1982-10-22 Fluorescent color ink for writing utensil

Country Status (1)

Country Link
JP (1) JPS5975967A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1311634A1 (en) * 2000-08-24 2003-05-21 Bic Corporation Solvent-based fluorescent inks for writing instruments based upon pigment dispersions in non-aqueous solvents

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52146303A (en) * 1976-05-26 1977-12-06 Pentel Kk Composition ink
JPS547825A (en) * 1977-06-21 1979-01-20 Ricoh Co Ltd Printer
JPS5472118A (en) * 1977-11-16 1979-06-09 Sakura Color Prod Corp Ink for marking pen
JPS56152878A (en) * 1980-04-28 1981-11-26 Pilot Ink Co Ltd Fluorescent ink for marking pen

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52146303A (en) * 1976-05-26 1977-12-06 Pentel Kk Composition ink
JPS547825A (en) * 1977-06-21 1979-01-20 Ricoh Co Ltd Printer
JPS5472118A (en) * 1977-11-16 1979-06-09 Sakura Color Prod Corp Ink for marking pen
JPS56152878A (en) * 1980-04-28 1981-11-26 Pilot Ink Co Ltd Fluorescent ink for marking pen

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1311634A1 (en) * 2000-08-24 2003-05-21 Bic Corporation Solvent-based fluorescent inks for writing instruments based upon pigment dispersions in non-aqueous solvents
EP1311634A4 (en) * 2000-08-24 2005-02-02 Bic Corp Solvent-based fluorescent inks for writing instruments based upon pigment dispersions in non-aqueous solvents
AU2001285100B2 (en) * 2000-08-24 2007-02-15 Bic Corporation Solvent-based fluorescent inks for writing instruments based upon pigment dispersions in non-aqueous solvents

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