JPH02123179A - Water-based ink - Google Patents
Water-based inkInfo
- Publication number
- JPH02123179A JPH02123179A JP63275503A JP27550388A JPH02123179A JP H02123179 A JPH02123179 A JP H02123179A JP 63275503 A JP63275503 A JP 63275503A JP 27550388 A JP27550388 A JP 27550388A JP H02123179 A JPH02123179 A JP H02123179A
- Authority
- JP
- Japan
- Prior art keywords
- water
- urea
- parts
- thiourea
- ink
- 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
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 30
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 74
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims abstract description 44
- 239000004202 carbamide Substances 0.000 claims abstract description 26
- 239000003086 colorant Substances 0.000 claims abstract description 5
- 238000001035 drying Methods 0.000 abstract description 7
- 238000001704 evaporation Methods 0.000 abstract description 2
- 230000008020 evaporation Effects 0.000 abstract description 2
- AOMZHDJXSYHPKS-UHFFFAOYSA-L disodium 4-amino-5-hydroxy-3-[(4-nitrophenyl)diazenyl]-6-phenyldiazenylnaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC2=CC(S([O-])(=O)=O)=C(N=NC=3C=CC=CC=3)C(O)=C2C(N)=C1N=NC1=CC=C([N+]([O-])=O)C=C1 AOMZHDJXSYHPKS-UHFFFAOYSA-L 0.000 abstract 1
- 239000000976 ink Substances 0.000 description 25
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- 230000000694 effects Effects 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical group CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000982 direct dye Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000003759 ester based solvent Substances 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Substances CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- 229950006389 thiodiglycol Drugs 0.000 description 1
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は水性インキ、特に蒸発を抑制し、長期間大気に
露出していても析出がなくかつ耐乾燥性に優れた特性を
有する水性インキに関するものである。[Detailed Description of the Invention] [Field of Industrial Application] The present invention relates to a water-based ink, particularly a water-based ink that suppresses evaporation, does not precipitate even when exposed to the atmosphere for a long period of time, and has excellent drying resistance. It is related to.
[従来の技術とその課題]
従来、水性インキで耐乾燥性を有するインキとしては、
グリコール系溶剤、グリコールエーテル系溶剤、グリコ
ールエーテルエステル系溶剤、アミン系溶剤等の水溶性
有機溶剤あるいは塩化リチウム又は塩化カルシウム等の
吸湿性無機化合物等をインキ組成成分として添加したも
のであったが。[Conventional technology and its issues] Conventionally, water-based inks with drying resistance include:
Water-soluble organic solvents such as glycol solvents, glycol ether solvents, glycol ether ester solvents, and amine solvents, or hygroscopic inorganic compounds such as lithium chloride or calcium chloride were added as ink composition components.
これらの化合物のみでは耐乾燥性が十分に満足するもの
が得られなかった。又耐乾燥性を向上するために尿素を
添加したものが知られているが、耐乾燥性を十分に満足
させるだけの尿素量を添加したインキでは経時において
尿素の結晶が析出してしまい、このインキを筆記具に用
いた場合、カスレや筆記不能というような問題を生じる
。It was not possible to obtain a product with sufficiently satisfactory drying resistance using only these compounds. In addition, inks containing urea added to improve drying resistance are known, but with inks that contain enough urea to fully satisfy drying resistance, urea crystals precipitate over time. When ink is used in writing instruments, problems such as blurring and inability to write arise occur.
[課題を解決するための手段] 本発明は前記問題点に鑑みなされたものであり。[Means to solve the problem] The present invention has been made in view of the above problems.
着色剤と、水と、尿素及びチオ尿素を混合比尿素:チオ
尿素=1:1〜9:1インキ全量に対し10重量%以上
とを少なくとも含有してなる水性インキを要旨とするも
のである。The gist is a water-based ink containing at least 10% by weight or more of a colorant, water, urea and thiourea in a mixed ratio of urea:thiourea = 1:1 to 9:1 based on the total amount of the ink. .
以下、本発明の各成分について詳述する。Each component of the present invention will be explained in detail below.
着色剤としては水溶性の醜性染料、直接染料あるいは塩
基性染料等のほとんどの染料及び一般に市販されている
顔料が1種又は2種以上を適宜選択して使用できる。そ
の使用量はインキ全量に対して1〜20重景%が好まし
い。As the colorant, one or more of most dyes such as water-soluble ugliness dyes, direct dyes, basic dyes, and generally commercially available pigments can be selected and used. The amount used is preferably 1 to 20% by weight based on the total amount of ink.
水は溶剤として用いるものであり、その使用量はインキ
全量に対して30〜80重量%が好ましい。 尿素及び
チオ尿素の混合比が尿素:チオ尿素=1=1〜9:1で
あるのは、尿素が1:1より少ないと十分な効果が得ら
れず、9:1より多いと析出という問題が起こる。又、
尿素及びチオ尿素の使用量がインキ全量に対して10重
量%以上であるのは、10重量%より少ないと十分な効
果が得られないためである。Water is used as a solvent, and the amount used is preferably 30 to 80% by weight based on the total amount of ink. The reason why the mixing ratio of urea and thiourea is urea:thiourea=1=1 to 9:1 is because if the urea content is less than 1:1, a sufficient effect cannot be obtained, and if the urea content is more than 9:1, precipitation will occur. happens. or,
The reason why the amount of urea and thiourea used is 10% by weight or more based on the total amount of the ink is that sufficient effects cannot be obtained if the amount is less than 10% by weight.
上記成分以外に水溶性有機溶剤、防腐剤、防錆剤、各種
界面活性剤、分散剤などを1種もしくは2種以上適宜使
用できるものである。In addition to the above components, one or more water-soluble organic solvents, preservatives, rust preventives, various surfactants, dispersants, etc. can be used as appropriate.
[作 用]
本発明の水性インキが何故結晶が析出しないのかについ
ては定かではないが、尿素分子中の酸素原子とチオ尿素
分子中の硫黄原子が水溶液中で引きあうことによって、
あたかも水の温度が上昇したのと同じ効果が現れ、尿素
及びチオ尿素の溶解度が高められることによって析出が
なく、耐乾燥性に優れたものになると思われる。[Function] It is not clear why crystals do not precipitate in the aqueous ink of the present invention, but the reason is that the oxygen atom in the urea molecule and the sulfur atom in the thiourea molecule attract each other in an aqueous solution.
It seems that the same effect appears as if the temperature of water were raised, and the solubility of urea and thiourea is increased, resulting in no precipitation and excellent drying resistance.
[実施例コ
以下に本発明を実施例により更に詳細に説明するが、実
施例中単に「部」とあるのは「重量部」を示すものであ
る。[Example] The present invention will be explained in more detail with reference to Examples below. In the Examples, the term "parts" simply indicates "parts by weight."
去m
エチレングリコール 20.0部水
56.8部
尿素 10.0部チオ尿
素 5.0部C,1,Ac
1d Black 2 8.0部スコアロー
ル900 0 、2部(界面活性剤、
花王■製)
上記各成分を40〜50℃に加温し、2時間撹拌するこ
とによって水性黒色インキを得た。Ethylene glycol 20.0 parts water
56.8 parts Urea 10.0 parts Thiourea 5.0 parts C,1,Ac
1d Black 2 8.0 parts Score Roll 900 0, 2 parts (surfactant,
(manufactured by Kao ■) The above components were heated to 40 to 50°C and stirred for 2 hours to obtain a water-based black ink.
匝較■上
実施例1の尿素及びチオ尿素の使用量をそれぞれ半分に
し、減らした分だけ水を増した以外は、実施例1ど同様
にして水性黒色インキを得た。Comparison (2) A water-based black ink was obtained in the same manner as in Example 1, except that the amounts of urea and thiourea used in Example 1 were each halved and the amount of water was increased by the reduced amount.
実−IIU2
グリセリン 5.0部水
57,8部
尿素 35.0部チオ尿
素 5.0部C,1,Ba
5ic Red 14 2.0部ブロクセル
GXL0.2部
(防腐剤、crc社製)
上記各成分を実施例1と同様にして水性赤色インキを得
た。Fruit-IIU2 Glycerin 5.0 parts Water
57,8 parts Urea 35.0 parts Thiourea 5.0 parts C,1,Ba
5ic Red 14 2.0 parts Broxel GXL 0.2 parts (preservative, manufactured by CRC) The above components were used in the same manner as in Example 1 to obtain a water-based red ink.
坦絞桝ス
実施例2のチオ尿素を除き、その分だけ水を増した以外
は実施例2と同様にして水性赤色、インキを得た。An aqueous red ink was obtained in the same manner as in Example 2 except that the thiourea in Example 2 was removed and the amount of water was increased accordingly.
太遣葛1
プロピレングリコール 7.0部チオジグ
リコール 5.0部水
60,8部尿素
12.0部チオ尿素
8.0部ベンゾトリアゾール
(防錆剤) 062部C,1,Direct B
lue 86 7.0部上記各成分を実施例1
と同様にして水性青色インキを得た。Taikyakuzu 1 Propylene glycol 7.0 parts Thiodiglycol 5.0 parts Water
60.8 parts urea 12.0 parts thiourea
8.0 parts Benzotriazole (rust inhibitor) 062 parts C, 1, Direct B
lue 86 7.0 parts Each of the above ingredients in Example 1
A water-based blue ink was obtained in the same manner as above.
災絞孤J
実施例3中の尿素及びチオ尿素を除き、その分だけ水を
増した以外は実施例3と同様にして水性青色インキを得
た。A water-based blue ink was obtained in the same manner as in Example 3 except that urea and thiourea in Example 3 were removed and water was increased accordingly.
失1珂エ
エチレングリコール 30.0部水
28.6部尿
素 20.0部チオ尿素
10.0部エチレン尿素(尿
素誘導体) 5.0部C,1,Ac1d Gr
een 19 6.0部ホルマリン(防腐剤)
0.4部上記各成分を実施例1と同
様にして水性緑色インキを得た。1 kake ethylene glycol 30.0 parts water
28.6 parts urea 20.0 parts thiourea
10.0 parts Ethylene urea (urea derivative) 5.0 parts C, 1, Ac1d Gr
een 19 6.0 parts formalin (preservative)
A water-based green ink was obtained using 0.4 parts of each of the above components in the same manner as in Example 1.
よ較史土
実施例4中の尿素を10.0部、チオ尿素を20.0部
とした以外は実施例4と同様にして水性緑色インキを得
た。A water-based green ink was obtained in the same manner as in Example 4, except that urea and thiourea in Example 4 were changed to 10.0 parts and 20.0 parts, respectively.
ル遣U11
実施例2中のチオ尿素を半分にし、減らした分だけ水を
加えた以外は実施例2と同様にして水性赤色インキを得
た。Example U11 A water-based red ink was obtained in the same manner as in Example 2, except that the amount of thiourea in Example 2 was halved and water was added in an amount corresponding to the reduced amount.
ル較涯且
実施例1中の尿素を除き、その量だけチオ尿素を加えた
以外は実施例1と同様にして水性黒色インキを得た。A water-based black ink was obtained in the same manner as in Example 1, except that urea in Example 1 was removed and thiourea was added in the same amount.
[効 果]
実施例1〜4.比較例1〜6により得られた水性インキ
を市販のべんてるサインペン 5520(ぺんてる■I
Iりに充填し、室温にて1週間放置後、ペン先の状態(
析出の有無)、及び筆跡にカ記録計用、スタンプ用、イ
ンキジェット記録用等のインキとしても使用可能なもの
である。[Effect] Examples 1 to 4. The water-based inks obtained in Comparative Examples 1 to 6 were applied to a commercially available Bentel felt-tip pen 5520 (Pentel I
After filling the container and leaving it at room temperature for a week, check the condition of the pen tip (
It can also be used as an ink for recording handwriting, stamps, inkjet recording, etc.
Claims (1)
尿素=1:1〜9:1でインキ全量に対し10重量%以
上とを少なくとも含有してなる水性インキ。A water-based ink containing at least a colorant, water, urea and thiourea at a mixing ratio of urea:thiourea of 1:1 to 9:1 and 10% by weight or more based on the total amount of the ink.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63275503A JPH02123179A (en) | 1988-10-31 | 1988-10-31 | Water-based ink |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63275503A JPH02123179A (en) | 1988-10-31 | 1988-10-31 | Water-based ink |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02123179A true JPH02123179A (en) | 1990-05-10 |
Family
ID=17556397
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63275503A Pending JPH02123179A (en) | 1988-10-31 | 1988-10-31 | Water-based ink |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02123179A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003525152A (en) * | 2000-03-02 | 2003-08-26 | コント | Writing implement provided with a drying retarder at the writing point and method for manufacturing the writing point |
EP2754702A1 (en) * | 2011-09-05 | 2014-07-16 | Nippon Kayaku Kabushiki Kaisha | Water-based black ink composition, inkjet recording method using same, and colored body |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5641261A (en) * | 1979-09-08 | 1981-04-17 | Sanyo Shikiso Kk | Pigment composition |
JPS5880368A (en) * | 1981-11-07 | 1983-05-14 | Sakura Color Prod Corp | Pigmented water-base ink composition for writing utensil |
-
1988
- 1988-10-31 JP JP63275503A patent/JPH02123179A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5641261A (en) * | 1979-09-08 | 1981-04-17 | Sanyo Shikiso Kk | Pigment composition |
JPS5880368A (en) * | 1981-11-07 | 1983-05-14 | Sakura Color Prod Corp | Pigmented water-base ink composition for writing utensil |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003525152A (en) * | 2000-03-02 | 2003-08-26 | コント | Writing implement provided with a drying retarder at the writing point and method for manufacturing the writing point |
EP2754702A1 (en) * | 2011-09-05 | 2014-07-16 | Nippon Kayaku Kabushiki Kaisha | Water-based black ink composition, inkjet recording method using same, and colored body |
EP2754702A4 (en) * | 2011-09-05 | 2015-04-22 | Nippon Kayaku Kk | Water-based black ink composition, inkjet recording method using same, and colored body |
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