CA1084653A - Ink composition for ink jet printing - Google Patents
Ink composition for ink jet printingInfo
- Publication number
- CA1084653A CA1084653A CA252,546A CA252546A CA1084653A CA 1084653 A CA1084653 A CA 1084653A CA 252546 A CA252546 A CA 252546A CA 1084653 A CA1084653 A CA 1084653A
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- CA
- Canada
- Prior art keywords
- ink
- ink composition
- composition
- glycol
- water
- 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.)
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
Abstract
INK COMPOSITION FOR
INK JET PRINTING
Abstract of the Disclosure There is disclosed an ink composition that is particularly suitable for ink jet printing. It comprises from 2 to 12% by weight of a water-soluble dye and from 35 to 80% by weight of at least one polyhydric alcohol having from 2 to 6 carbon atoms and water. The ink composition has a viscosity of 4 to 20 centipoises at 25°C.
The ink composition may further include an antiseptic and a non-ionic surface active agent.
INK JET PRINTING
Abstract of the Disclosure There is disclosed an ink composition that is particularly suitable for ink jet printing. It comprises from 2 to 12% by weight of a water-soluble dye and from 35 to 80% by weight of at least one polyhydric alcohol having from 2 to 6 carbon atoms and water. The ink composition has a viscosity of 4 to 20 centipoises at 25°C.
The ink composition may further include an antiseptic and a non-ionic surface active agent.
Description
~ ~ ~ 65i3 I Backglound of the Invention I . - ~
l This invention relates to an ink composition for ink jet ¦printing, and more particularly to an aqueous ink cornposition ¦for use in an ink jet printing system of a type which involves ¦projecting an ink from a srQall nozzle by rapidly or instantane-¦ously reduciny -an inner vol~ne of an iTIk~holding container.
¦ An ink jet printing system of the ts~pe mentioned above is ¦known, for example, in British patent speci~ication No. 1,350,83 ~.
¦Broadly speaking, the jet system of the British patent specifi-¦cation includes the following two steps: first, an inner vol~me ¦of a small container filled with an ink ~s rapidly or ins~an-¦taneously reduced by means of an electric driving pulse to force the ink droplet to be projected from a nozzle tip so that one ~ ink droplet is deposited on recording paper every driving pulse (first step); and after completion of the jetting, the system is entirely then returned to an initial state and stands ready for a subsequent jet opexation (second step).
Ink compositions to be employed in the ink jet printing system of the cla~s just mentioned should meet at least the ~ followiny charackeristic requirements similarly to inks for use r.. "
in other types of ink jet recording systems:
. 1. Being free frorn cloggin~ in the nozzle.
l This invention relates to an ink composition for ink jet ¦printing, and more particularly to an aqueous ink cornposition ¦for use in an ink jet printing system of a type which involves ¦projecting an ink from a srQall nozzle by rapidly or instantane-¦ously reduciny -an inner vol~ne of an iTIk~holding container.
¦ An ink jet printing system of the ts~pe mentioned above is ¦known, for example, in British patent speci~ication No. 1,350,83 ~.
¦Broadly speaking, the jet system of the British patent specifi-¦cation includes the following two steps: first, an inner vol~me ¦of a small container filled with an ink ~s rapidly or ins~an-¦taneously reduced by means of an electric driving pulse to force the ink droplet to be projected from a nozzle tip so that one ~ ink droplet is deposited on recording paper every driving pulse (first step); and after completion of the jetting, the system is entirely then returned to an initial state and stands ready for a subsequent jet opexation (second step).
Ink compositions to be employed in the ink jet printing system of the cla~s just mentioned should meet at least the ~ followiny charackeristic requirements similarly to inks for use r.. "
in other types of ink jet recording systems:
. 1. Being free frorn cloggin~ in the nozzle.
2. Ensuring a sharp contrast upon recording.
3. Neither changing in physical property nor pxoducing any precipitates during storage. .
In adaition, it is found that the ink for use in the ink jet systeZQ of the above-mentioned type is essentially requixed to have suitable ranges o~ a viscosity and a surface tension sv as to attain a satisfactory ink jet recording. Paxticular~y, A~
1 ,~ " ., '' " ."''.' ''' '. ''' ' ''" ' ' ' .': , '.,: ' .
. . . .... . .
--` li ~OB46~i;3 the viscosity of an ink gives a great influence on the recording For example, ~lhen an ink i~ used having a viscosity outside a ¦
suitable range which is usually determined depending on the type of an emplo~ed apparatus and the kind of electric driving pulses to be input, the above-mentioned first and second steps do not proceed smoothly by the reasons described kereinbelow, it being thus difficult to effect the ink jet recording satisfactorily.
That is, ~ith an ink having a viscosity below a suitable range, it is almost impossible in the first step to correct a speed variation or deviation in the respective portions of an elongate I
~ink droplet being ejected from a nozzle tip. As a consequence, two or more ink droplets with different ~elocities are undesirab e projected in correspondence with one electric driving pulse.
~ If the nozæle tip is positioned at a relatively great distance lS from a-recording mediurn, the two or more drop]ets are deposited on the recording medium in different points to form correspondin different dots thereon, lowering the quality of the resulting ;-~
print or image considerably. Further, an ink having a viscosity below a sultable range also impedes a smooth operation in the $econd step. That is, after completion of the ~etting of the ink droplet,`an ink meniscus is temporarily lowered by the reaction of the ink jetting. The meniscus then rises or is ~eturned to an oriyinal state by the action of capillary force.
In this connection, however, if the ink viscosity is too low, the ink does not satisfactorily serves as a damper. Thus, it undesirable takes a relatively long period of time until the ink meniscus settles down in an equilibrium position. This is because the ink meniscus will pass over a level of the nozæle tip and be then pulled down by the ac-tion of surface tension force, repeatincJ the vibration damping type behavior so as to . , ' . ': ' ,:
, ' ' . ' . ' ' , :
.. ..
:, . .
R9~653 restore a standstill position thereof. On the contrary, with an ink havin~ too high viscosity-, it does not show any v;bration damping type behavior, but requires a long period of tlme before being pulled back hy the action of capillary force. In either case, the returning to an initial or ready-to-jet state of the ink takes an unfavorably long period of time, lowering a printing speed. -A number of ink composition for ink jet printing have been heretofore proposed but most of them fall short of one or more of the above-mentioned requirements and have thus inherent disadvantages which must be overcome. For example, there is known an ink composition to`which is added a water-soluble thickner so as to maintain a viscosity of the composition at a desired viscosity. ~lowever, the water soluble thickner which includes, for example, a cellulose derivative such as hydxoxyl- --propyl cellulose, carboxylmethyl cellulose, hydroxylethyl cellulose, methyl cellulose or the like, or polyvinyl alcohol tends to change a viscosity of the ink composition or, in some cases, to produce precipitates during storage in combination with a water-soluble dye or coloring agent: This is practically disadvantages in the application to the ink jet system in which the change in the viscosity exerts a detrimental influence in carrying out the process oE the system. In the ink jet system, it is general to use a nozzle with a diameter as small as 30 `25 to 200 ~. With such fine noæzle construction, the nozzle is readily clogged due to precipitation of solid matter resulting from evaporation of solvent when the composition is present or stayed in the noæzle. Further, the air corresponding to the amount of an evaporated solvent may enter a nozzle tip and ~30 remain in a head as bubble5. This will impede a sharp ink jct - _ 4 _ . ' `~ ~ .
response to an inner volume change caused by an electric driv-ing pulse. As a result, no injection of an ink takes place, or the injection conditions or state varies with a lapse of time, so that it becomes difficult to effect the recording in a stable state.
Moreover, the United States Patent No. 3,705,043 discloses an aqueous ink composition which includes 1 to 8~ by weight of a water-soluble dye and 5 to 30% by weight of a wetting agent such as polyethylene glycol, polypropylene glycol, ethylene glycol, propylene glycol, diethylene glycol, glycerol or the like. However, such small amount of the wetting agent is not sufficient to maintain the composition in a viscosity range required for the intended ink jet system. In addition, even with the aqueous ink composition, it is hard to prevent both the nozzle from being clogged and the air from entering the nozzle tip.
Brief Summary of The Invention In accordance with one aspect of this invention there is provided an ink composition for ink jet printing, consisting essentially of 2 to 12% by weight of a water-soluble dye and a mixed solvent consisting of water and 35 to 80% by weight of a polyhydric alcohol having at least two hydroxyl groups and having 2 to 6 carbon atoms, said composition having a viscosity of 4 to 20 centipoises at 25C.
In accordance with another aspect of this invention there is provided an ink composition for ink jet printing obtained by dissolving in water a mixture comprising a water-soluble dye and at least one polyhydric alcohol having 2 - 6 carbon atoms to form an aqueous solution having a viscosity of 4 to 20 centipoises at 25C, removing solid particulates with a size above 1 ~ contained in the solution by filtration to obtain a second solution and removing gases dissolved _ ~, 5 /i :, ' .. , ' ,, . ' : ' , , '"` !l .
6~3 l ,~
in second solution by placing the second solution under ~ -reduced pressure.
.. I ,.
~ Detailed Description of the Invention '',..... . .
.,`:', : A preferred e~xx~ment of the invention is constitute by an aqueous ink cc~position which comprises 2 to 12 % by weight of a w~
¦soluble dye, 35 to 80 % by weight of a polyhydric alcohol ' ¦containing from 2 to 6 carbon atoms, and water. The aqueous ¦ink composition has a viscosity of 4 to 20 centipoises at 25C
¦and meets all th~ characteristic requirements mentioned herein-lQ ¦before.
¦ The water-soluble dyes useful in the present in~ention are - ¦those which are soluble in a solvent system composed of the polyhydric alcohol and water, in an amount above 2 % by w~ight based on the solvent system. With monochromic recording, black or blue dyes are preferred so as to render great a contrast on recording paper. Black dyes are, for example, C.I. Direct Black 17, 38 and 51, C.I. Acid Blac]c 2, 7, 24, 31, 52, 107, 118 119 and 156, and blue dyes are C.I. Direct Blue 1, 6, 15, 25, 71, 86 and 226, C.I. Acid Blue 9, 62,'102, 104, 113, 117, and 120, C.I. Basic Blue 1l 3, 5, 7, 9 and ~8, and the like. These may be used'singly or in combination. The amount of the dye is not particularly important so far as it is within a range sufficient to offer a clear contrast upon application onto recording paper. With the amount below 2 wt ~, applied dye spots or dots on recording paper becomes unclear when the sic~e of injected ink droplets i5 too small. While, the amount above 12 wt ~ is not necessary in practicaJ application and is rat}ler - 6 - ' ' . , '. ', . :, ' , , ' - ~, , : ' . ' ~ ' . ' ' ' . .
~ ~ 53 ¦unfavorable since the dye dissolved in such large amount tends to be precipitated by evaporation of the solvent system though ¦the tendency is dependent on a composition of the solvent systern ¦ Examples o~ the polyhydric a]cohols suitable for the ¦practice of the invention ethylene glycol, propylene glycol, ¦trimethylene glycol, glycerine; 1,3-butanediol, 2,3-butanediol, ¦1,4-butanediol, diethylene glycol, 1,5-pentanediol, hexylene ¦glycol, triethylene glycol, aipropylene glycol, 1,2,6-hexanetrio ¦and the like. These polyhydric alcohols may be used singly ¦or in combination. All of the above-mentioned polyhydric ¦alcohols are miscible'with water in any arbitrary ratio and play ~- ¦an important role in the ink composition of the invention to - ¦satisfy the afore-mentioned characteristic requirements because ¦of their inherent properties such as high hygrospicity, 10~J
l-i, ~ Y
¦~apor pressure and high thic~Q~ property. The amount of the polyhydric alcohol varies depending on a desired viscosity of ¦the ink composition, the amount and kind of the water-soluble ¦dye and the degree of reducing or preventing the nozzle from ~ -' being clogged or the air from entering the nozzle. In order to meet the afore-mentioned requirements, the amount is required to be in the'ra~ge of from 35 to 80 ~ by weight of the ink composition. ~iith the arnount below 35 wt %, the ink composit:ion ,results, in most cases, in lower viscosity than the defined range and the nozzle clogging and bubble entering can not be prevented satis~actorily though the viscosity and preventincj effects may vary depending on the amount of dyes and the kind of polyhydric alcohols. On the contrary, use of the polyhydric alcohol in an amount ahove 80 ~7t ~ will undesirably increas~
the viscosity of the ink composition In cither cas~, the ~noun t of the polyh7dric alc~hol outside the above-deined range rn~y ~n~;
.:
i53 cause infeasibility of printing, reduction in printing speed and production of defective printed matter. ~.
As will be understood from the above, the ink composition of the invention comprises a water-soluble dye and a polyhydric alcohol in the form of an aqueous solution In addition thereto, the ink composition may further comprise various kinds of additives, if necesSary. For example, if it is assumed that it takes a long period of storage time before the ink composition is actually used, the composition may be added with an antiseptic so as to.prevent or reduce the growth of b~cteria therein. A number of antiseptics are- known to ~ be useful for this purpose, of which Dioxin (trade rnark for 2,6-dimethyl-m-dioxan-4-ol acetate) is preferable:. The amount.
of the antiseptic i5 generally below 1% by weight, preferably in the range of 0.01 to 0.5% by weight, of the total amount of the ink composition.
Further, surface acti~e agents may be added to the ink composition of the invention in ~rder to.improve the surface tension of the ink and the "wetting" of the ink to 20 ink passages. Any surface active agents may be used without restriction unless they react with the dye employed. Non-ionic active agents are preferred including commeraially available polyoxyalkylenes-and alkyl ethers thereof, siloxane- - .
~; oxyalkylene copol~ners (L-5340*, product of Union Carbide Co.), .: :
fluorine-containing surface active agents (FC - 430*, product .
o~ 3~ Co.~, and the like. These surface active agents are generally used in an amount below 1% by weight, preferably 0.05 to 0.5% by weight, of the total amount of the ink composi-tion. ..
In order to prepare the ink composition of the inven- `
tion, it is important to mix the composition uniformly under agitating conditions sufficient to dissolve the water-soluble dye * trade rnarks -8-,.. ,,, .. , ..... . ~ ..... . . . .
.
.
V13~653 Further, after completion of the mi.xing, it is desirable to 1, provide a filtration step for removing insoluble matters from the uniform mixture. If the solid.and fine particulate matters such as insoluble dye and dust or contaminant from outside are .
not removed by filtration, the smooth passage of the ink .
. composition through a nozzie upon application may be impeded, . resulting in no or abnoxmal injection of the ink.
. In order to overcome the impedient, it is preferable to remove solid particulates with a size above 5 ~, preferably above 1 ~ though the size may vary~depending on the diameter . of an employed nozzle. A filter medium is properly selected -.~ :
. depending on the size of solid particulates to be r~moved.
esentative o the filter medium is, for examp].e, "fluorinert ~ :.
FA" (membrane filter made of polyfluoroethylene and produced ~:
~by Millipore Co.). . ~ -. - In practising the invention, it is also desirable that : the ink be prepared wi.thout dissolving therein a large amount of air. If a large amount of air is dissolved in the ink . . composition, air bubbles may be produced during the res.idence .
of the ink composition in a print head, hindering a normal ink .
.in~ection and thus making it dif~cult to efect a stable ...
recording operation by the reasons described hereinbeore. In this connection, however, it is general that a small amount of : :
air is inevitably dissolved in the ink compo9ition during the : ~ -.
course of the production process under agitating conditions. . .
The dissolved air should preferably be removed by a suitable ; - method such as degassing by placing the ink composition under reduced pressure. Though the degassing may be efected either : prior to or after thc filtration step, it is preferable to de~as after the fil1:ration step since air may be dissolved in , .
, - g ~
. ~ r ~
., .. . .
.
1~ ~ ~
the filtration step. I
¦ The present invention will be particularly illustrated by I -l way of the followin~ ex~nples.
'., I ~ , , .
¦ Example 1 ¦ .640 g of cthylenc glycol and 319 g of clistilled ~ater were ¦ placed in a 2 Q Erle.nmeyer flask equipped with an agitator, ¦to ~hich was further added 1 g of dioxine with agitation. ~fter ¦the dioxine had been completely dissolved in the system, 40 g ¦of Nigrosine dye (C.I. Acid Black 2) was.gradually added to the . .:
.10 ¦solution with agitatlon, followed by agitatlon for further 2 .-.- ¦hours at room temperature. The resulting solution ~as fed to ; Ia filter having a fluorirlert filter mediu.m having pore s~ze of ¦1.0 ~ by means of a pressure pump to filter at a rate of 20 ml . ¦per min. The filtrate was then placed in a 2 Q pressure vessel ~ .
:15 which had been cleaned by washing. The inner pressure of the vessel was reduced to about 20 mmHg by means of an aspirator and maintained at the same level for lO.min for deyassiny, after :
which the inner pressure was gradually returned to a normal press~lre to obtain an ink. The thus obtai.ned ink had the :
:20 followiny composition, viscosity and sur~ace tension.
: Composition: ethylene glycol64.0 wt distilled water31.9 "
. Nigrosine 4.0 "
D l~ Y~
-~.~ O. 1 11 Vi~cosity: 7.03 c.p.s. (25C) . Surface Tension: ~7.7 dynes/cm (25C) Then, the jet recordin~ was effected by the use oE an apparatus deiscri.bed on the Bxitish paten~ speci~ication No.
1,350,836 (p~r~icularly shown i.n Figs. 1 - 3 and de.-:cri.bed at ~ ~o .. ~ . . .
',.'' ~ 8~6~i3 ¦line 28 on ~age 2 to line 94 on page 3). That is, the ink was ¦poured in the apparatus having the following parameters for ¦jet recording. As a result, clear black printed matters with la high contrast could be obtained. No change in quality ¦occurred when the jet reco~ding was continued over 24 hours.
¦Further~ when the recording was again effected 3 weeks after ¦completion of the first recording, no abnormality such as ¦elogging of nozzle was recognized, with printed matters w~th ¦such invariable and high quality as those obtained in the :10 ¦first recording operation.
¦ Parameters:
printing rate ~ 2000 dQts/sec statie pressure 0.006 psi peak pulse pressure 4.83 psi pulse voltage 65 V - -~- pulse width ~ 135 ~s orifiee diameter 0.0028 inches ' - ' . ' . ' ''" . '' Example 2 ~
The procedure of Example 1 was repeated to obtain an ink -having the followiny eomposition, Composition:
, propylene glycol , 40.0 wt distilled ~ater 56.9 "
S~ninol milliny black 3.0 "
VLG (produced by S~nitomo Kagaku K.K.) , p,~
' ~ , ~ , 0.1"
; Viseosity: 4.77 e.p.s. (25C) Surface Tension: 48.6 dynes/em (25C) , ' ',, '", 1~ L6S3 . The jet recording was conducted by using the apparatus en~ployed in Exarnple 1 haviny the following parameters and added ~ -with the above ink composition. As a result, good results were obtained similarly to those of Example 1. ¦-. 5 Parameters: . ~ .
. printi.ng rate . . 1408.dots/sec static pressure 0.006 psi 1~ :
peak pulse pressure 8.06 psi -pulse voltage 120 V ¦::
]0 pulse width 130 ~s ,~ :
orifice diameter 0.00~6 inches -~ ' '' i"' ~ .
Exarnple 3 ~ ~ :.
. ::
The procedure of Example 1 was repeated to obtain an ink . .
. having the following composition. ~ :.:
-Composition: . . .
glycerine10.0 wt ~
ethylene glycol 5~.0 " ..
a, stilled water . 29.9 "
Nigrosine . 8.0 "
20 ~ ~ loxine ~ 0.1 "
Vi~cosity: 10.9 c.p.s. (25C) , . , Surface Tension: ~7.9 dynes/crn. (25C) .
The jet récording was conducted by the use of the apparatus o~ Example 1 haviny the following parameters and applied with the above ink composition. As a result, good results were . . . obtained sirnilarly to those o Example 1, with a higher print .~ . density.
. _ . ' :' . , .
. ~ , . 12 ~ ~
..
Parameter~
printing rate 1754 dots/sec static pressure 0.006 psi peak pulse pressure 5.74 psi pulse voltage 80 V
pulse width 140 ~ s orifice diameter 0.0028 inches Example 4 The general procedure-of Example was repeated for the 10 preparation of an ink having the following composition.
Composition diethylene glycol 43.0 wt %
distilled water 52.8 ~I
Kayarus Turquo se 3.0 "
Blue GL (product of Nippon Kayaku K.K.)-Kayarus Supra Blue 1.0 "
; FF2GL (product of Nippon Kayaku K.K.) Surfactant FC-430* ~ 0.1 "
(product of 3M Co.) Dioxin 0.1 Viscosity: 7.00 c.p.s. (25C) Surface Tension: 23.5 dynes/cm (25C) .: . ~ . .
Then, the jet recording was conducted by ~he use of thP apparatus of Example 1 having the following parameters-and applied with the above ink composition. As a result, good results were obtained similarly to those of Example 1, with blue in print color.
Parameters:
printing xate 172~ dots/sec , ~ static pressure 0.006 psi - *trade mark ~13-, .. .. . .
.~
. ' . , " :
, ~ 10~34653 ~ peak pulse pressure 4.71 psi : . pulse voltage Ç5 V
: . pulse width . 1~0 ~s :~.
. ' orifice diameter 0.0028 inches :~
. . , ~ . , ,:' . 5 . Example 5 - . - . .- . ..
The procedure of Example 1 was repeated to ob~ain an ink .having the following composition. . , , :'~
~ Composition: - ' :; .ethylene glycol, ~ 75.0 Wt % ' ].0 '~ distilled water :20.9 " : ~ .
Nigrosine .'4.0 "
: ~ . D~ 0.1 " . ' . ........... ~iscosity: 10.4 c.p.s. (25C~ .'.:, . Sur~ace Tension: 49.4 dynes/cm (25C) ' ~15The ink jet recording was conducted by the use of the . apparatus of Example 1 having the following parameters and :: applied with the above ink composition. As a result, good . results were obtained similarly to those of Example 1.
~' ~ Parameters: , ' . , print.ing rate ' 1369 dots/sec .
. st~'tic pressure 0.006 p-,i . ., ~ . . . .
., . ~ ' peak pulse pressu~e 7.42 psi .. ~ , .` . pulse voltage 110 V
pulse width 130 ~s ' 2s ~ orifice dlameter 0-0039 inches '~ . , , ;
. `, .
':~
Ir ~
. . .
' , . :
'
In adaition, it is found that the ink for use in the ink jet systeZQ of the above-mentioned type is essentially requixed to have suitable ranges o~ a viscosity and a surface tension sv as to attain a satisfactory ink jet recording. Paxticular~y, A~
1 ,~ " ., '' " ."''.' ''' '. ''' ' ''" ' ' ' .': , '.,: ' .
. . . .... . .
--` li ~OB46~i;3 the viscosity of an ink gives a great influence on the recording For example, ~lhen an ink i~ used having a viscosity outside a ¦
suitable range which is usually determined depending on the type of an emplo~ed apparatus and the kind of electric driving pulses to be input, the above-mentioned first and second steps do not proceed smoothly by the reasons described kereinbelow, it being thus difficult to effect the ink jet recording satisfactorily.
That is, ~ith an ink having a viscosity below a suitable range, it is almost impossible in the first step to correct a speed variation or deviation in the respective portions of an elongate I
~ink droplet being ejected from a nozzle tip. As a consequence, two or more ink droplets with different ~elocities are undesirab e projected in correspondence with one electric driving pulse.
~ If the nozæle tip is positioned at a relatively great distance lS from a-recording mediurn, the two or more drop]ets are deposited on the recording medium in different points to form correspondin different dots thereon, lowering the quality of the resulting ;-~
print or image considerably. Further, an ink having a viscosity below a sultable range also impedes a smooth operation in the $econd step. That is, after completion of the ~etting of the ink droplet,`an ink meniscus is temporarily lowered by the reaction of the ink jetting. The meniscus then rises or is ~eturned to an oriyinal state by the action of capillary force.
In this connection, however, if the ink viscosity is too low, the ink does not satisfactorily serves as a damper. Thus, it undesirable takes a relatively long period of time until the ink meniscus settles down in an equilibrium position. This is because the ink meniscus will pass over a level of the nozæle tip and be then pulled down by the ac-tion of surface tension force, repeatincJ the vibration damping type behavior so as to . , ' . ': ' ,:
, ' ' . ' . ' ' , :
.. ..
:, . .
R9~653 restore a standstill position thereof. On the contrary, with an ink havin~ too high viscosity-, it does not show any v;bration damping type behavior, but requires a long period of tlme before being pulled back hy the action of capillary force. In either case, the returning to an initial or ready-to-jet state of the ink takes an unfavorably long period of time, lowering a printing speed. -A number of ink composition for ink jet printing have been heretofore proposed but most of them fall short of one or more of the above-mentioned requirements and have thus inherent disadvantages which must be overcome. For example, there is known an ink composition to`which is added a water-soluble thickner so as to maintain a viscosity of the composition at a desired viscosity. ~lowever, the water soluble thickner which includes, for example, a cellulose derivative such as hydxoxyl- --propyl cellulose, carboxylmethyl cellulose, hydroxylethyl cellulose, methyl cellulose or the like, or polyvinyl alcohol tends to change a viscosity of the ink composition or, in some cases, to produce precipitates during storage in combination with a water-soluble dye or coloring agent: This is practically disadvantages in the application to the ink jet system in which the change in the viscosity exerts a detrimental influence in carrying out the process oE the system. In the ink jet system, it is general to use a nozzle with a diameter as small as 30 `25 to 200 ~. With such fine noæzle construction, the nozzle is readily clogged due to precipitation of solid matter resulting from evaporation of solvent when the composition is present or stayed in the noæzle. Further, the air corresponding to the amount of an evaporated solvent may enter a nozzle tip and ~30 remain in a head as bubble5. This will impede a sharp ink jct - _ 4 _ . ' `~ ~ .
response to an inner volume change caused by an electric driv-ing pulse. As a result, no injection of an ink takes place, or the injection conditions or state varies with a lapse of time, so that it becomes difficult to effect the recording in a stable state.
Moreover, the United States Patent No. 3,705,043 discloses an aqueous ink composition which includes 1 to 8~ by weight of a water-soluble dye and 5 to 30% by weight of a wetting agent such as polyethylene glycol, polypropylene glycol, ethylene glycol, propylene glycol, diethylene glycol, glycerol or the like. However, such small amount of the wetting agent is not sufficient to maintain the composition in a viscosity range required for the intended ink jet system. In addition, even with the aqueous ink composition, it is hard to prevent both the nozzle from being clogged and the air from entering the nozzle tip.
Brief Summary of The Invention In accordance with one aspect of this invention there is provided an ink composition for ink jet printing, consisting essentially of 2 to 12% by weight of a water-soluble dye and a mixed solvent consisting of water and 35 to 80% by weight of a polyhydric alcohol having at least two hydroxyl groups and having 2 to 6 carbon atoms, said composition having a viscosity of 4 to 20 centipoises at 25C.
In accordance with another aspect of this invention there is provided an ink composition for ink jet printing obtained by dissolving in water a mixture comprising a water-soluble dye and at least one polyhydric alcohol having 2 - 6 carbon atoms to form an aqueous solution having a viscosity of 4 to 20 centipoises at 25C, removing solid particulates with a size above 1 ~ contained in the solution by filtration to obtain a second solution and removing gases dissolved _ ~, 5 /i :, ' .. , ' ,, . ' : ' , , '"` !l .
6~3 l ,~
in second solution by placing the second solution under ~ -reduced pressure.
.. I ,.
~ Detailed Description of the Invention '',..... . .
.,`:', : A preferred e~xx~ment of the invention is constitute by an aqueous ink cc~position which comprises 2 to 12 % by weight of a w~
¦soluble dye, 35 to 80 % by weight of a polyhydric alcohol ' ¦containing from 2 to 6 carbon atoms, and water. The aqueous ¦ink composition has a viscosity of 4 to 20 centipoises at 25C
¦and meets all th~ characteristic requirements mentioned herein-lQ ¦before.
¦ The water-soluble dyes useful in the present in~ention are - ¦those which are soluble in a solvent system composed of the polyhydric alcohol and water, in an amount above 2 % by w~ight based on the solvent system. With monochromic recording, black or blue dyes are preferred so as to render great a contrast on recording paper. Black dyes are, for example, C.I. Direct Black 17, 38 and 51, C.I. Acid Blac]c 2, 7, 24, 31, 52, 107, 118 119 and 156, and blue dyes are C.I. Direct Blue 1, 6, 15, 25, 71, 86 and 226, C.I. Acid Blue 9, 62,'102, 104, 113, 117, and 120, C.I. Basic Blue 1l 3, 5, 7, 9 and ~8, and the like. These may be used'singly or in combination. The amount of the dye is not particularly important so far as it is within a range sufficient to offer a clear contrast upon application onto recording paper. With the amount below 2 wt ~, applied dye spots or dots on recording paper becomes unclear when the sic~e of injected ink droplets i5 too small. While, the amount above 12 wt ~ is not necessary in practicaJ application and is rat}ler - 6 - ' ' . , '. ', . :, ' , , ' - ~, , : ' . ' ~ ' . ' ' ' . .
~ ~ 53 ¦unfavorable since the dye dissolved in such large amount tends to be precipitated by evaporation of the solvent system though ¦the tendency is dependent on a composition of the solvent systern ¦ Examples o~ the polyhydric a]cohols suitable for the ¦practice of the invention ethylene glycol, propylene glycol, ¦trimethylene glycol, glycerine; 1,3-butanediol, 2,3-butanediol, ¦1,4-butanediol, diethylene glycol, 1,5-pentanediol, hexylene ¦glycol, triethylene glycol, aipropylene glycol, 1,2,6-hexanetrio ¦and the like. These polyhydric alcohols may be used singly ¦or in combination. All of the above-mentioned polyhydric ¦alcohols are miscible'with water in any arbitrary ratio and play ~- ¦an important role in the ink composition of the invention to - ¦satisfy the afore-mentioned characteristic requirements because ¦of their inherent properties such as high hygrospicity, 10~J
l-i, ~ Y
¦~apor pressure and high thic~Q~ property. The amount of the polyhydric alcohol varies depending on a desired viscosity of ¦the ink composition, the amount and kind of the water-soluble ¦dye and the degree of reducing or preventing the nozzle from ~ -' being clogged or the air from entering the nozzle. In order to meet the afore-mentioned requirements, the amount is required to be in the'ra~ge of from 35 to 80 ~ by weight of the ink composition. ~iith the arnount below 35 wt %, the ink composit:ion ,results, in most cases, in lower viscosity than the defined range and the nozzle clogging and bubble entering can not be prevented satis~actorily though the viscosity and preventincj effects may vary depending on the amount of dyes and the kind of polyhydric alcohols. On the contrary, use of the polyhydric alcohol in an amount ahove 80 ~7t ~ will undesirably increas~
the viscosity of the ink composition In cither cas~, the ~noun t of the polyh7dric alc~hol outside the above-deined range rn~y ~n~;
.:
i53 cause infeasibility of printing, reduction in printing speed and production of defective printed matter. ~.
As will be understood from the above, the ink composition of the invention comprises a water-soluble dye and a polyhydric alcohol in the form of an aqueous solution In addition thereto, the ink composition may further comprise various kinds of additives, if necesSary. For example, if it is assumed that it takes a long period of storage time before the ink composition is actually used, the composition may be added with an antiseptic so as to.prevent or reduce the growth of b~cteria therein. A number of antiseptics are- known to ~ be useful for this purpose, of which Dioxin (trade rnark for 2,6-dimethyl-m-dioxan-4-ol acetate) is preferable:. The amount.
of the antiseptic i5 generally below 1% by weight, preferably in the range of 0.01 to 0.5% by weight, of the total amount of the ink composition.
Further, surface acti~e agents may be added to the ink composition of the invention in ~rder to.improve the surface tension of the ink and the "wetting" of the ink to 20 ink passages. Any surface active agents may be used without restriction unless they react with the dye employed. Non-ionic active agents are preferred including commeraially available polyoxyalkylenes-and alkyl ethers thereof, siloxane- - .
~; oxyalkylene copol~ners (L-5340*, product of Union Carbide Co.), .: :
fluorine-containing surface active agents (FC - 430*, product .
o~ 3~ Co.~, and the like. These surface active agents are generally used in an amount below 1% by weight, preferably 0.05 to 0.5% by weight, of the total amount of the ink composi-tion. ..
In order to prepare the ink composition of the inven- `
tion, it is important to mix the composition uniformly under agitating conditions sufficient to dissolve the water-soluble dye * trade rnarks -8-,.. ,,, .. , ..... . ~ ..... . . . .
.
.
V13~653 Further, after completion of the mi.xing, it is desirable to 1, provide a filtration step for removing insoluble matters from the uniform mixture. If the solid.and fine particulate matters such as insoluble dye and dust or contaminant from outside are .
not removed by filtration, the smooth passage of the ink .
. composition through a nozzie upon application may be impeded, . resulting in no or abnoxmal injection of the ink.
. In order to overcome the impedient, it is preferable to remove solid particulates with a size above 5 ~, preferably above 1 ~ though the size may vary~depending on the diameter . of an employed nozzle. A filter medium is properly selected -.~ :
. depending on the size of solid particulates to be r~moved.
esentative o the filter medium is, for examp].e, "fluorinert ~ :.
FA" (membrane filter made of polyfluoroethylene and produced ~:
~by Millipore Co.). . ~ -. - In practising the invention, it is also desirable that : the ink be prepared wi.thout dissolving therein a large amount of air. If a large amount of air is dissolved in the ink . . composition, air bubbles may be produced during the res.idence .
of the ink composition in a print head, hindering a normal ink .
.in~ection and thus making it dif~cult to efect a stable ...
recording operation by the reasons described hereinbeore. In this connection, however, it is general that a small amount of : :
air is inevitably dissolved in the ink compo9ition during the : ~ -.
course of the production process under agitating conditions. . .
The dissolved air should preferably be removed by a suitable ; - method such as degassing by placing the ink composition under reduced pressure. Though the degassing may be efected either : prior to or after thc filtration step, it is preferable to de~as after the fil1:ration step since air may be dissolved in , .
, - g ~
. ~ r ~
., .. . .
.
1~ ~ ~
the filtration step. I
¦ The present invention will be particularly illustrated by I -l way of the followin~ ex~nples.
'., I ~ , , .
¦ Example 1 ¦ .640 g of cthylenc glycol and 319 g of clistilled ~ater were ¦ placed in a 2 Q Erle.nmeyer flask equipped with an agitator, ¦to ~hich was further added 1 g of dioxine with agitation. ~fter ¦the dioxine had been completely dissolved in the system, 40 g ¦of Nigrosine dye (C.I. Acid Black 2) was.gradually added to the . .:
.10 ¦solution with agitatlon, followed by agitatlon for further 2 .-.- ¦hours at room temperature. The resulting solution ~as fed to ; Ia filter having a fluorirlert filter mediu.m having pore s~ze of ¦1.0 ~ by means of a pressure pump to filter at a rate of 20 ml . ¦per min. The filtrate was then placed in a 2 Q pressure vessel ~ .
:15 which had been cleaned by washing. The inner pressure of the vessel was reduced to about 20 mmHg by means of an aspirator and maintained at the same level for lO.min for deyassiny, after :
which the inner pressure was gradually returned to a normal press~lre to obtain an ink. The thus obtai.ned ink had the :
:20 followiny composition, viscosity and sur~ace tension.
: Composition: ethylene glycol64.0 wt distilled water31.9 "
. Nigrosine 4.0 "
D l~ Y~
-~.~ O. 1 11 Vi~cosity: 7.03 c.p.s. (25C) . Surface Tension: ~7.7 dynes/cm (25C) Then, the jet recordin~ was effected by the use oE an apparatus deiscri.bed on the Bxitish paten~ speci~ication No.
1,350,836 (p~r~icularly shown i.n Figs. 1 - 3 and de.-:cri.bed at ~ ~o .. ~ . . .
',.'' ~ 8~6~i3 ¦line 28 on ~age 2 to line 94 on page 3). That is, the ink was ¦poured in the apparatus having the following parameters for ¦jet recording. As a result, clear black printed matters with la high contrast could be obtained. No change in quality ¦occurred when the jet reco~ding was continued over 24 hours.
¦Further~ when the recording was again effected 3 weeks after ¦completion of the first recording, no abnormality such as ¦elogging of nozzle was recognized, with printed matters w~th ¦such invariable and high quality as those obtained in the :10 ¦first recording operation.
¦ Parameters:
printing rate ~ 2000 dQts/sec statie pressure 0.006 psi peak pulse pressure 4.83 psi pulse voltage 65 V - -~- pulse width ~ 135 ~s orifiee diameter 0.0028 inches ' - ' . ' . ' ''" . '' Example 2 ~
The procedure of Example 1 was repeated to obtain an ink -having the followiny eomposition, Composition:
, propylene glycol , 40.0 wt distilled ~ater 56.9 "
S~ninol milliny black 3.0 "
VLG (produced by S~nitomo Kagaku K.K.) , p,~
' ~ , ~ , 0.1"
; Viseosity: 4.77 e.p.s. (25C) Surface Tension: 48.6 dynes/em (25C) , ' ',, '", 1~ L6S3 . The jet recording was conducted by using the apparatus en~ployed in Exarnple 1 haviny the following parameters and added ~ -with the above ink composition. As a result, good results were obtained similarly to those of Example 1. ¦-. 5 Parameters: . ~ .
. printi.ng rate . . 1408.dots/sec static pressure 0.006 psi 1~ :
peak pulse pressure 8.06 psi -pulse voltage 120 V ¦::
]0 pulse width 130 ~s ,~ :
orifice diameter 0.00~6 inches -~ ' '' i"' ~ .
Exarnple 3 ~ ~ :.
. ::
The procedure of Example 1 was repeated to obtain an ink . .
. having the following composition. ~ :.:
-Composition: . . .
glycerine10.0 wt ~
ethylene glycol 5~.0 " ..
a, stilled water . 29.9 "
Nigrosine . 8.0 "
20 ~ ~ loxine ~ 0.1 "
Vi~cosity: 10.9 c.p.s. (25C) , . , Surface Tension: ~7.9 dynes/crn. (25C) .
The jet récording was conducted by the use of the apparatus o~ Example 1 haviny the following parameters and applied with the above ink composition. As a result, good results were . . . obtained sirnilarly to those o Example 1, with a higher print .~ . density.
. _ . ' :' . , .
. ~ , . 12 ~ ~
..
Parameter~
printing rate 1754 dots/sec static pressure 0.006 psi peak pulse pressure 5.74 psi pulse voltage 80 V
pulse width 140 ~ s orifice diameter 0.0028 inches Example 4 The general procedure-of Example was repeated for the 10 preparation of an ink having the following composition.
Composition diethylene glycol 43.0 wt %
distilled water 52.8 ~I
Kayarus Turquo se 3.0 "
Blue GL (product of Nippon Kayaku K.K.)-Kayarus Supra Blue 1.0 "
; FF2GL (product of Nippon Kayaku K.K.) Surfactant FC-430* ~ 0.1 "
(product of 3M Co.) Dioxin 0.1 Viscosity: 7.00 c.p.s. (25C) Surface Tension: 23.5 dynes/cm (25C) .: . ~ . .
Then, the jet recording was conducted by ~he use of thP apparatus of Example 1 having the following parameters-and applied with the above ink composition. As a result, good results were obtained similarly to those of Example 1, with blue in print color.
Parameters:
printing xate 172~ dots/sec , ~ static pressure 0.006 psi - *trade mark ~13-, .. .. . .
.~
. ' . , " :
, ~ 10~34653 ~ peak pulse pressure 4.71 psi : . pulse voltage Ç5 V
: . pulse width . 1~0 ~s :~.
. ' orifice diameter 0.0028 inches :~
. . , ~ . , ,:' . 5 . Example 5 - . - . .- . ..
The procedure of Example 1 was repeated to ob~ain an ink .having the following composition. . , , :'~
~ Composition: - ' :; .ethylene glycol, ~ 75.0 Wt % ' ].0 '~ distilled water :20.9 " : ~ .
Nigrosine .'4.0 "
: ~ . D~ 0.1 " . ' . ........... ~iscosity: 10.4 c.p.s. (25C~ .'.:, . Sur~ace Tension: 49.4 dynes/cm (25C) ' ~15The ink jet recording was conducted by the use of the . apparatus of Example 1 having the following parameters and :: applied with the above ink composition. As a result, good . results were obtained similarly to those of Example 1.
~' ~ Parameters: , ' . , print.ing rate ' 1369 dots/sec .
. st~'tic pressure 0.006 p-,i . ., ~ . . . .
., . ~ ' peak pulse pressu~e 7.42 psi .. ~ , .` . pulse voltage 110 V
pulse width 130 ~s ' 2s ~ orifice dlameter 0-0039 inches '~ . , , ;
. `, .
':~
Ir ~
. . .
' , . :
'
Claims (5)
1. An ink composition for ink jet printing, consisting essentially of 2 to 12% by weight of a water-soluble dye and a mixed solvent consisting of water and 35 to 80% by weight of at least one polyhydric alcohol having at least two hydroxyl groups and having 2 to 6 carbon atoms, said composition having a viscosity of 4 to 20 centipoises at 25°C.
2. The ink composition according to claim 1, wherein said at least one polyhydric alcohol is selected from the group consisting of ethylene glycol, propylene glycol, tri-methylene glycol, glycerine, 1,3-butanediol, 2,3-butanediol, 1,4-butanediol, diethylene glycol, 1,5-pentanediol, hexylene glycol, triethylene glycol, dipropylene glycol and 1,2,6-hexanetriol.
3. The ink composition of claim 1 further comprising 0.01 - 1 wt % of an antiseptic.
4. The ink composition according to claim 3, wherein said antiseptic is 2,6-dimethyl-m-dioxan-4-ol acetate.
5. The ink composition of claim 3 further comprising 0.05 - 1 wt % of a non-ionic surface active agent.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50061691A JPS51137506A (en) | 1975-05-22 | 1975-05-22 | Composition of ink for ink jet recording |
| JP61691/75 | 1975-05-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1084653A true CA1084653A (en) | 1980-09-02 |
Family
ID=13178520
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA252,546A Expired CA1084653A (en) | 1975-05-22 | 1976-05-14 | Ink composition for ink jet printing |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4176361A (en) |
| JP (1) | JPS51137506A (en) |
| CA (1) | CA1084653A (en) |
| DE (1) | DE2622352B2 (en) |
| GB (1) | GB1551324A (en) |
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| US4281329A (en) * | 1978-06-20 | 1981-07-28 | Canon Kabushiki Kaisha | Liquid recording medium |
| US4196006A (en) * | 1978-09-08 | 1980-04-01 | Whittaker Corporation | Jet printing ink |
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| JPS5657862A (en) * | 1979-10-17 | 1981-05-20 | Seiko Epson Corp | Ink for ink-jet recording |
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-
1975
- 1975-05-22 JP JP50061691A patent/JPS51137506A/en active Granted
-
1976
- 1976-05-12 US US05/685,629 patent/US4176361A/en not_active Expired - Lifetime
- 1976-05-14 CA CA252,546A patent/CA1084653A/en not_active Expired
- 1976-05-17 GB GB20341/76A patent/GB1551324A/en not_active Expired
- 1976-05-19 DE DE2622352A patent/DE2622352B2/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| DE2622352C3 (en) | 1979-01-04 |
| DE2622352A1 (en) | 1976-12-02 |
| JPS5618396B2 (en) | 1981-04-28 |
| GB1551324A (en) | 1979-08-30 |
| US4176361A (en) | 1979-11-27 |
| DE2622352B2 (en) | 1978-04-20 |
| JPS51137506A (en) | 1976-11-27 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |