JPS644550B2 - - Google Patents
Info
- Publication number
- JPS644550B2 JPS644550B2 JP16550181A JP16550181A JPS644550B2 JP S644550 B2 JPS644550 B2 JP S644550B2 JP 16550181 A JP16550181 A JP 16550181A JP 16550181 A JP16550181 A JP 16550181A JP S644550 B2 JPS644550 B2 JP S644550B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- viscosity
- ink composition
- ink
- aqueous 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.)
- Expired
Links
- 239000000203 mixture Substances 0.000 claims description 18
- 125000005702 oxyalkylene group Chemical group 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000006353 oxyethylene group Chemical group 0.000 claims description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000000976 ink Substances 0.000 description 24
- 150000001875 compounds Chemical class 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- UZZFFIUHUDOYPS-UHFFFAOYSA-L disodium 4-amino-3,6-bis[[4-[(2,4-diaminophenyl)diazenyl]phenyl]diazenyl]-5-oxido-7-sulfonaphthalene-2-sulfonate Chemical compound [Na+].[Na+].Nc1ccc(N=Nc2ccc(cc2)N=Nc2c(N)c3c(O)c(N=Nc4ccc(cc4)N=Nc4ccc(N)cc4N)c(cc3cc2S([O-])(=O)=O)S([O-])(=O)=O)c(N)c1 UZZFFIUHUDOYPS-UHFFFAOYSA-L 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 238000005342 ion exchange Methods 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- AVERNFJXXRIVQN-XSDYUOFFSA-N 5-[(4-ethoxyphenyl)diazenyl]-2-[(e)-2-[4-[(4-ethoxyphenyl)diazenyl]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound C1=CC(OCC)=CC=C1N=NC(C=C1S(O)(=O)=O)=CC=C1\C=C\C1=CC=C(N=NC=2C=CC(OCC)=CC=2)C=C1S(O)(=O)=O AVERNFJXXRIVQN-XSDYUOFFSA-N 0.000 description 1
- IURGIPVDZKDLIX-UHFFFAOYSA-M [7-(diethylamino)phenoxazin-3-ylidene]-diethylazanium;chloride Chemical compound [Cl-].C1=CC(=[N+](CC)CC)C=C2OC3=CC(N(CC)CC)=CC=C3N=C21 IURGIPVDZKDLIX-UHFFFAOYSA-M 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- VJDDAARZIFHSQY-UHFFFAOYSA-N basic black 2 Chemical compound [Cl-].C=1C2=[N+](C=3C=CC=CC=3)C3=CC(N(CC)CC)=CC=C3N=C2C=CC=1NN=C1C=CC(=O)C=C1 VJDDAARZIFHSQY-UHFFFAOYSA-N 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 239000000982 direct dye Substances 0.000 description 1
- 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 description 1
- YCMOBGSVZYLYBZ-UHFFFAOYSA-L disodium 5-[[4-[4-[(2-amino-8-hydroxy-6-sulfonatonaphthalen-1-yl)diazenyl]phenyl]phenyl]diazenyl]-2-hydroxybenzoate Chemical compound NC1=CC=C2C=C(C=C(O)C2=C1N=NC1=CC=C(C=C1)C1=CC=C(C=C1)N=NC1=CC=C(O)C(=C1)C(=O)O[Na])S(=O)(=O)O[Na] YCMOBGSVZYLYBZ-UHFFFAOYSA-L 0.000 description 1
- NJHFCEDUNPPBHI-UHFFFAOYSA-L disodium 6-[(4-cyclohexyl-2-methylphenyl)diazenyl]-4-[(4-methylphenyl)sulfonylamino]-5-oxido-7-sulfonaphthalene-2-sulfonate Chemical compound CC1=CC=C(C=C1)S(=O)(=O)NC2=C3C(=CC(=C2)S(=O)(=O)[O-])C=C(C(=C3[O-])N=NC4=C(C=C(C=C4)C5CCCCC5)C)S(=O)(=O)O.[Na+].[Na+] NJHFCEDUNPPBHI-UHFFFAOYSA-L 0.000 description 1
- OOYIOIOOWUGAHD-UHFFFAOYSA-L disodium;2',4',5',7'-tetrabromo-4,5,6,7-tetrachloro-3-oxospiro[2-benzofuran-1,9'-xanthene]-3',6'-diolate Chemical compound [Na+].[Na+].O1C(=O)C(C(=C(Cl)C(Cl)=C2Cl)Cl)=C2C21C1=CC(Br)=C([O-])C(Br)=C1OC1=C(Br)C([O-])=C(Br)C=C21 OOYIOIOOWUGAHD-UHFFFAOYSA-L 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- SEACYXSIPDVVMV-UHFFFAOYSA-L eosin Y Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 SEACYXSIPDVVMV-UHFFFAOYSA-L 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- -1 glycol ethers Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- MCPLVIGCWWTHFH-UHFFFAOYSA-L methyl blue Chemical compound [Na+].[Na+].C1=CC(S(=O)(=O)[O-])=CC=C1NC1=CC=C(C(=C2C=CC(C=C2)=[NH+]C=2C=CC(=CC=2)S([O-])(=O)=O)C=2C=CC(NC=3C=CC(=CC=3)S([O-])(=O)=O)=CC=2)C=C1 MCPLVIGCWWTHFH-UHFFFAOYSA-L 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- RBYJOOWYRXEJAM-UHFFFAOYSA-M sodium;5,9-dianilino-7-phenylbenzo[a]phenazin-7-ium-4,10-disulfonate Chemical compound [Na+].C=1C=CC=CC=1[N+]1=C2C=C(NC=3C=CC=CC=3)C(S(=O)(=O)[O-])=CC2=NC(C2=CC=CC(=C22)S([O-])(=O)=O)=C1C=C2NC1=CC=CC=C1 RBYJOOWYRXEJAM-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- FKVXIGHJGBQFIH-UHFFFAOYSA-K trisodium 5-amino-3-[[4-[4-[(7-amino-1-hydroxy-3-sulfonatonaphthalen-2-yl)diazenyl]phenyl]phenyl]diazenyl]-4-hydroxynaphthalene-2,7-disulfonate Chemical compound C1=CC(=CC=C1C2=CC=C(C=C2)N=NC3=C(C=C4C=CC(=CC4=C3[O-])N)S(=O)(=O)O)N=NC5=C(C6=C(C=C(C=C6C=C5S(=O)(=O)O)S(=O)(=O)[O-])N)[O-].[Na+].[Na+].[Na+] FKVXIGHJGBQFIH-UHFFFAOYSA-K 0.000 description 1
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Description
本発明は水性インキ組成物に関するものであ
る。
従来、インクジエツト、サインペン、ボールペ
ン、フエルトペン等に使用されている水性インキ
組成物には、染料の溶解性を高めて目詰りを防止
するため、あるいは保湿性を高めてインキの急速
な乾燥を防止するために、エチレングリコール、
プロピレングリコール、グリセリン等の多価アル
コール類、ジエチレングリコール、トリエチレン
グリコール、ポリエチレングリコール等のポリグ
リコール類、メチルセロソルブ、メチルカルビト
ール、メチルトリグリコール等のグリコールエー
テル類が使用されてきた。これらの溶剤は水によ
く溶け、沸点が高いという特徴を持つているが、
水溶液の粘度の温度による変化が大きく、使用す
る温度によつては、にじんだり、かすれたり、紙
にひつかかり過ぎたりする等の問題があつた。
本発明は以上のような従来のものの問題点を解
決するためになされたもので、特定のアルコキシ
プロパンジオールまたはそのオキシアルキレン誘
導体を含有させることにより、温度による粘度変
化が少なく、このため季節、地方が変つてもほと
んど同じような書き味を示し、にじんだり、かす
れたり、紙にひつかかり過ぎることのない水性イ
ンキ組成物を提供することを目的としている。
本発明は一般式(1)で示されるアルコキシプロパ
ンジオールまたはそのオキシアルキレン誘導体を
含有することを特徴とする水性インキ組成物であ
る。
(ただし、Rは炭素数1〜4のアルキル基、
AOは炭素数2または3のオキシアルキレン基、
a+bは0〜10である。)
一般式(1)において、炭素数1〜4のアルキル基
としては、メチル基、エチル基、n―プロピル
基、イソプロピル基、n―ブチル基、イソブチル
基、ターシヤリーブチル基などがあり、炭素数2
または3のオキシアルキレン基としては、オキシ
エチレン、オキシプロピレンなどがある。これら
はそれぞれ1種単独、または複数の混合物であつ
てもよい。
Rで示されるアルキル基の炭素数が4以下に限
定されるのは5以上では界面活性が強くなり、目
詰りやインキの切れの原因となる発泡を引起こす
からである。
a,bは(AO)で示されるオキシアルキレン
基の平均付加モル数を示し、それぞれ0の場合を
含む。すなわち一般式(1)の化合物は、オキシアル
キレンを付加しないアルコキシプロパンジオール
を使用してもよいが、沸点、引火点を高くする目
的で、アルコキシプロパンジオールにアルキレン
オキシドを付加してもよい。この場合、その付加
量は10モル以下である必要がある。その理由は10
モルを越えると水溶液の粘度の温度による変化が
大きくなつてしまうからである。
本発明の水性インキ組成物は、以上の一般式(1)
で示されるアルコキシプロパンジオールまたはそ
のオキシアルキレン誘導体を水溶性染料と配合し
た組成物である。アルコキシプロパンジオールま
たはそのオキシアルキレン誘導体の使用量は2〜
60重量%である。
また染料としては、水溶性染料であればいかな
る染料も使用可能である。例えば直接染料として
は、C.I.ダイレクトブラツク19,51,108,194、
ダイレクトブルー2,93,98ダイレクトレツド
1,17,28、ダイレクトイエロー12,24、酸性染
料としてはC.I.アシツドブラツク2,31,52、ア
シツドブルー59,93,103、アシツドレツド87,
92,155、塩基性染料としては、C.I.ベーシツク
ブラツク2,8、ベーシツクブルー3,7、ベー
シツクレツド18,52等があげられる。
本発明の水性インキ組成物には、安定剤、殺菌
剤、表面張力調整剤などの他の添加剤を配合する
ことも可能である。
本発明はインクジエツト、サインペン、ボール
ペン、フエルトペン、その他の用途に使用される
水性インキ組成物に適用可能である。
以上のとおり、本発明の水性インキ組成物は、
温度による粘度変化が少なく、季節、地域による
使用感が一定したものであり、にじみ、かすれ、
ひつかかり過ぎがないなどの効果がある。
以下に実施例を記載してさらに詳細に説明す
る。
実施例 1
表1に示す化合物の25重量%水溶液を作り、0
〜40℃の範囲で粘度を測定した。その結果を図面
のグラフおよび表2に示す。
The present invention relates to a water-based ink composition. Conventionally, water-based ink compositions used in inkjet, felt-tip pens, ballpoint pens, felt-tip pens, etc. have been designed to increase dye solubility to prevent clogging, or to increase moisture retention to prevent ink from drying out quickly. In order to, ethylene glycol,
Polyhydric alcohols such as propylene glycol and glycerin, polyglycols such as diethylene glycol, triethylene glycol and polyethylene glycol, and glycol ethers such as methyl cellosolve, methyl carbitol and methyl triglycol have been used. These solvents are characterized by being highly soluble in water and having a high boiling point.
The viscosity of the aqueous solution changes greatly depending on the temperature, and depending on the temperature used, there are problems such as smearing, blurring, and sticking to paper too much. The present invention was made to solve the problems of the conventional products as described above, and by containing a specific alkoxypropanediol or its oxyalkylene derivative, the viscosity changes little due to temperature, and therefore it can be used in different seasons and regions. The purpose of the present invention is to provide an aqueous ink composition that exhibits almost the same writing quality even when the ink composition changes, and that does not smear, blur, or stick to paper too much. The present invention is an aqueous ink composition characterized by containing an alkoxypropanediol represented by general formula (1) or an oxyalkylene derivative thereof. (However, R is an alkyl group having 1 to 4 carbon atoms,
AO is an oxyalkylene group having 2 or 3 carbon atoms,
a+b is 0-10. ) In general formula (1), examples of the alkyl group having 1 to 4 carbon atoms include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, isobutyl group, and tert-butyl group. Number 2
Examples of the oxyalkylene group of 3 include oxyethylene and oxypropylene. Each of these may be used alone or as a mixture of a plurality of them. The reason why the number of carbon atoms in the alkyl group represented by R is limited to 4 or less is that if it is 5 or more, the surface activity becomes strong, causing foaming that causes clogging and ink running out. a and b represent the average number of added moles of the oxyalkylene group represented by (AO), including the case where each is 0. That is, for the compound of general formula (1), an alkoxypropanediol to which no oxyalkylene is added may be used, but an alkylene oxide may be added to the alkoxypropanediol for the purpose of increasing the boiling point and flash point. In this case, the amount added needs to be 10 moles or less. The reasons are 10
This is because if the amount exceeds mol, the viscosity of the aqueous solution will vary greatly depending on the temperature. The aqueous ink composition of the present invention has the above general formula (1).
This is a composition in which an alkoxypropanediol or its oxyalkylene derivative represented by the formula is blended with a water-soluble dye. The amount of alkoxypropanediol or its oxyalkylene derivative used is 2 to 2.
It is 60% by weight. Further, as the dye, any water-soluble dye can be used. For example, direct dyes include CI Direct Black 19, 51, 108, 194,
Direct Blue 2, 93, 98 Direct Red 1, 17, 28, Direct Yellow 12, 24, CI Acid Black 2, 31, 52, Acid Blue 59, 93, 103, Acid Red 87,
92, 155, and basic dyes include CI Basic Black 2, 8, Basic Blue 3, 7, Basic Cred 18, 52, and the like. The aqueous ink composition of the present invention can also contain other additives such as stabilizers, bactericides, surface tension regulators, and the like. The present invention is applicable to aqueous ink compositions used for ink jets, felt-tip pens, ballpoint pens, felt pens, and other uses. As described above, the water-based ink composition of the present invention is
There is little change in viscosity due to temperature, and the feeling of use is consistent depending on the season and region.
It has the effect of not being too tight. Examples will be described below in further detail. Example 1 A 25% by weight aqueous solution of the compounds shown in Table 1 was prepared, and 0
Viscosity was measured in the range ~40°C. The results are shown in the graph of the drawing and in Table 2.
【表】【table】
【表】【table】
【表】
図面および表2の結果より、本発明品の水溶液
粘度の温度変化が少ないことは明らかである。
実施例 2
C.I.ダイレクトブラツク19 3.0%
表1中No.1の化合物 25.0〃
イオン交換水 72.0〃
上述の組成物を常温で混合して黒色インキを得
た。比較例として表1中No.1の化合物の代りにグ
リセリンを用いて黒色インキを作つた。得られた
2種のインキの粘度を測定した結果は以下の通り
であり、実施例によるものの粘度の変化は小さか
つた。また実施例のインクはにじんだり、かすれ
たりすることはなく、優れた書き味であつた。
0℃粘度(cSt)
40℃粘度(cSt)
実施例 5.2
2.9
比較例 5.6
1.3
実施例 3
C.I.アシツドブルー93 2.0%
表1中No.5の化合物 22.0〃
イオン交換水 76.0〃
上述の組成物、および比較例として表1中No.5
の化合物の代りにポリエチレングリコール(分子
量200)を使用し、前例と同様に2種の青色イン
キを得た。2種のインキの粘度は以下に示す通り
であり、実施例によるものの粘度の変化は小さか
つた。また、実施例のインクはにじんだり、かす
れたりすることはなく、優れた書き味であつた。
0℃粘度(cSt)
40℃粘度(cSt)
実施例 4.8
2.8
比較例 5.8
1.5
実施例 4
C.I.ベーシツクレツド52 1.0%
表1中No.6の化合物 20.0〃
イオン交換水 79.0〃
上述の組成物、および比較例として表1中No.6
の化合物の代りにプロピレングリコールを使用
し、前例と同様に2種の赤インキを得た。2種の
赤インキの粘度は以下に示す通りであり、実施例
によるものの粘度の変化は小さかつた。また、実
施例のインクはにじんだり、かすれたりすること
はなく、優れた書き味であつた。
0℃粘度(cSt)
40℃粘度(cSt)
実施例 5.0
3.1
比較例 5.0
1.0[Table] From the results shown in the drawings and Table 2, it is clear that the temperature change in the aqueous solution viscosity of the product of the present invention is small. Example 2 CI Direct Black 19 3.0% Compound No. 1 in Table 1 25.0 Ion-exchanged water 72.0 The above compositions were mixed at room temperature to obtain a black ink. As a comparative example, a black ink was prepared using glycerin instead of compound No. 1 in Table 1. The results of measuring the viscosity of the two types of ink obtained are as follows, and the change in viscosity of the ink according to the example was small. Furthermore, the ink of the example did not bleed or fade, and had an excellent writing feel. 0℃ viscosity (cSt)
Viscosity at 40℃ (cSt) Example 5.2
2.9 Comparative Example 5.6
1.3 Example 3 CI Acid Blue 93 2.0% Compound No. 5 in Table 1 22.0〃 Ion exchange water 76.0〃 The above composition and No. 5 in Table 1 as a comparative example
Two types of blue inks were obtained in the same manner as in the previous example, using polyethylene glycol (molecular weight 200) instead of the compound. The viscosity of the two types of ink is as shown below, and the change in viscosity of the ink according to the example was small. Further, the ink of the example did not bleed or fade, and had an excellent writing feel. 0℃ viscosity (cSt)
Viscosity at 40℃ (cSt) Example 4.8
2.8 Comparative example 5.8
1.5 Example 4 CI Basic Cred 52 1.0% Compound No. 6 in Table 1 20.0〃 Ion exchange water 79.0〃 The above composition and No. 6 in Table 1 as a comparative example
Two types of red inks were obtained in the same manner as in the previous example, using propylene glycol instead of the compound. The viscosities of the two types of red inks are as shown below, and the changes in viscosity of those according to the examples were small. Further, the ink of the example did not bleed or fade, and had an excellent writing feel. 0℃ viscosity (cSt)
Viscosity at 40℃ (cSt) Example 5.0
3.1 Comparative example 5.0
1.0
図面は実施例1における温度と粘度の関係を示
すグラフである。
The drawing is a graph showing the relationship between temperature and viscosity in Example 1.
Claims (1)
ールまたはそのオキシアルキレン誘導体を含有す
ることを特徴とする水性インキ組成物。 (ただし、Rは炭素数1〜4のアルキル基、
AOは炭素数2または3のオキシアルキレン基、
a+bは0〜10である。) 2 Rはメチル基、エチル基、n―プロピル基、
イソプロピル基、n―ブチル基、イソブチル基、
およびターシヤリーブチル基から選ばれる1種ま
たは数種の基である特許請求の範囲第1項記載の
水性インキ組成物。 3 AOはオキシエチレンおよびオキシプロピレ
ンから選ばれる1種または数種の基である特許請
求の範囲第1項または第2項記載の水性インキ組
成物。[Scope of Claims] 1. An aqueous ink composition characterized by containing an alkoxypropanediol represented by general formula (1) or an oxyalkylene derivative thereof. (However, R is an alkyl group having 1 to 4 carbon atoms,
AO is an oxyalkylene group having 2 or 3 carbon atoms,
a+b is 0-10. ) 2 R is a methyl group, an ethyl group, an n-propyl group,
Isopropyl group, n-butyl group, isobutyl group,
The aqueous ink composition according to claim 1, wherein the aqueous ink composition is one or more groups selected from and tertiary butyl groups. 3. The aqueous ink composition according to claim 1 or 2, wherein AO is one or more groups selected from oxyethylene and oxypropylene.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16550181A JPS5867770A (en) | 1981-10-16 | 1981-10-16 | Water-based ink composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16550181A JPS5867770A (en) | 1981-10-16 | 1981-10-16 | Water-based ink composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5867770A JPS5867770A (en) | 1983-04-22 |
| JPS644550B2 true JPS644550B2 (en) | 1989-01-26 |
Family
ID=15813585
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16550181A Granted JPS5867770A (en) | 1981-10-16 | 1981-10-16 | Water-based ink composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5867770A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH03167686A (en) * | 1989-10-23 | 1991-07-19 | Internatl Business Mach Corp <Ibm> | Method and apparatus for measuring efficiency of engineer |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6032866A (en) * | 1983-08-03 | 1985-02-20 | Seiko Epson Corp | Ink for ink jet recording |
| JPS62169875A (en) * | 1986-01-23 | 1987-07-27 | Toray Ind Inc | Ink composition for use in ink jet recording |
-
1981
- 1981-10-16 JP JP16550181A patent/JPS5867770A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH03167686A (en) * | 1989-10-23 | 1991-07-19 | Internatl Business Mach Corp <Ibm> | Method and apparatus for measuring efficiency of engineer |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5867770A (en) | 1983-04-22 |
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