JPH02206661A - Ink composition - Google Patents
Ink compositionInfo
- Publication number
- JPH02206661A JPH02206661A JP1025066A JP2506689A JPH02206661A JP H02206661 A JPH02206661 A JP H02206661A JP 1025066 A JP1025066 A JP 1025066A JP 2506689 A JP2506689 A JP 2506689A JP H02206661 A JPH02206661 A JP H02206661A
- Authority
- JP
- Japan
- Prior art keywords
- ink
- composition
- antioxidant
- vehicle
- ink composition
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 39
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 18
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 16
- 238000002844 melting Methods 0.000 claims abstract description 13
- 239000007787 solid Substances 0.000 claims abstract description 13
- 239000000463 material Substances 0.000 claims abstract description 12
- 230000008018 melting Effects 0.000 claims abstract description 12
- 238000004040 coloring Methods 0.000 claims abstract description 8
- 239000007788 liquid Substances 0.000 claims description 4
- 235000013824 polyphenols Nutrition 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 4
- 229940057995 liquid paraffin Drugs 0.000 abstract description 3
- 239000004203 carnauba wax Substances 0.000 abstract description 2
- 235000013869 carnauba wax Nutrition 0.000 abstract description 2
- 239000012530 fluid Substances 0.000 abstract 1
- 238000011156 evaluation Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000012188 paraffin wax Substances 0.000 description 6
- 230000000740 bleeding effect Effects 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 235000019271 petrolatum Nutrition 0.000 description 4
- 239000001993 wax Substances 0.000 description 4
- AMPCGOAFZFKBGH-UHFFFAOYSA-O [4-[[4-(dimethylamino)phenyl]-[4-(methylamino)phenyl]methylidene]cyclohexa-2,5-dien-1-ylidene]-dimethylazanium Chemical compound C1=CC(NC)=CC=C1C(C=1C=CC(=CC=1)N(C)C)=C1C=CC(=[N+](C)C)C=C1 AMPCGOAFZFKBGH-UHFFFAOYSA-O 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- 230000000903 blocking effect Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 230000004044 response Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- HXIQYSLFEXIOAV-UHFFFAOYSA-N 2-tert-butyl-4-(5-tert-butyl-4-hydroxy-2-methylphenyl)sulfanyl-5-methylphenol Chemical compound CC1=CC(O)=C(C(C)(C)C)C=C1SC1=CC(C(C)(C)C)=C(O)C=C1C HXIQYSLFEXIOAV-UHFFFAOYSA-N 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 2
- 239000004264 Petrolatum Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 150000008430 aromatic amides Chemical class 0.000 description 2
- -1 aromatic sulfonamides Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- ZXJXZNDDNMQXFV-UHFFFAOYSA-M crystal violet Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1[C+](C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 ZXJXZNDDNMQXFV-UHFFFAOYSA-M 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000012943 hotmelt Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000004200 microcrystalline wax Substances 0.000 description 2
- 235000019808 microcrystalline wax Nutrition 0.000 description 2
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 2
- DMCJFWXGXUEHFD-UHFFFAOYSA-N pentatriacontan-18-one Chemical compound CCCCCCCCCCCCCCCCCC(=O)CCCCCCCCCCCCCCCCC DMCJFWXGXUEHFD-UHFFFAOYSA-N 0.000 description 2
- 229940066842 petrolatum Drugs 0.000 description 2
- 239000002530 phenolic antioxidant Substances 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229940124530 sulfonamide Drugs 0.000 description 2
- 238000004781 supercooling Methods 0.000 description 2
- ROVRRJSRRSGUOL-UHFFFAOYSA-N victoria blue bo Chemical compound [Cl-].C12=CC=CC=C2C(NCC)=CC=C1C(C=1C=CC(=CC=1)N(CC)CC)=C1C=CC(=[N+](CC)CC)C=C1 ROVRRJSRRSGUOL-UHFFFAOYSA-N 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 1
- GJDRKHHGPHLVNI-UHFFFAOYSA-N 2,6-ditert-butyl-4-(diethoxyphosphorylmethyl)phenol Chemical compound CCOP(=O)(OCC)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 GJDRKHHGPHLVNI-UHFFFAOYSA-N 0.000 description 1
- YCMLQMDWSXFTIF-UHFFFAOYSA-N 2-methylbenzenesulfonimidic acid Chemical compound CC1=CC=CC=C1S(N)(=O)=O YCMLQMDWSXFTIF-UHFFFAOYSA-N 0.000 description 1
- PRWJPWSKLXYEPD-UHFFFAOYSA-N 4-[4,4-bis(5-tert-butyl-4-hydroxy-2-methylphenyl)butan-2-yl]-2-tert-butyl-5-methylphenol Chemical compound C=1C(C(C)(C)C)=C(O)C=C(C)C=1C(C)CC(C=1C(=CC(O)=C(C=1)C(C)(C)C)C)C1=CC(C(C)(C)C)=C(O)C=C1C PRWJPWSKLXYEPD-UHFFFAOYSA-N 0.000 description 1
- QPQKUYVSJWQSDY-UHFFFAOYSA-N 4-phenyldiazenylaniline Chemical compound C1=CC(N)=CC=C1N=NC1=CC=CC=C1 QPQKUYVSJWQSDY-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 239000004255 Butylated hydroxyanisole Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ORAWFNKFUWGRJG-UHFFFAOYSA-N Docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(N)=O ORAWFNKFUWGRJG-UHFFFAOYSA-N 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- YCUVUDODLRLVIC-UHFFFAOYSA-N Sudan black B Chemical compound C1=CC(=C23)NC(C)(C)NC2=CC=CC3=C1N=NC(C1=CC=CC=C11)=CC=C1N=NC1=CC=CC=C1 YCUVUDODLRLVIC-UHFFFAOYSA-N 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 description 1
- 235000019282 butylated hydroxyanisole Nutrition 0.000 description 1
- 229940043253 butylated hydroxyanisole Drugs 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- INSRQEMEVAMETL-UHFFFAOYSA-N decane-1,1-diol Chemical compound CCCCCCCCCC(O)O INSRQEMEVAMETL-UHFFFAOYSA-N 0.000 description 1
- SVTDYSXXLJYUTM-UHFFFAOYSA-N disperse red 9 Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC SVTDYSXXLJYUTM-UHFFFAOYSA-N 0.000 description 1
- ILRSCQWREDREME-UHFFFAOYSA-N dodecanamide Chemical compound CCCCCCCCCCCC(N)=O ILRSCQWREDREME-UHFFFAOYSA-N 0.000 description 1
- GTZOYNFRVVHLDZ-UHFFFAOYSA-N dodecane-1,1-diol Chemical compound CCCCCCCCCCCC(O)O GTZOYNFRVVHLDZ-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000005499 meniscus Effects 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000004043 responsiveness Effects 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- LMYRWZFENFIFIT-UHFFFAOYSA-N toluene-4-sulfonamide Chemical compound CC1=CC=C(S(N)(=O)=O)C=C1 LMYRWZFENFIFIT-UHFFFAOYSA-N 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- 239000010981 turquoise Substances 0.000 description 1
- 239000001043 yellow dye Substances 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、インクジェット記録装置に用いられるインク
組成物に関する。さらに詳しくは、常温より高温の状態
の下でインクジェット記録が行われるインク組成物に関
する。
【従来の技術〕
インクジェット記録は、記録時における静粛性と高速印
字性に優れている。従来よりインクジェット記録用のイ
ンク組成物として、水等を基剤とした液体のインク組成
物が使われている。しかしながら、紙にしみこむことに
よって記録されることから、インクのしみこみ易い紙へ
の記録ではにじみを生じてしまい、記録ドツトの周辺が
不鮮明で印字品質が低下するという欠点を有している。
この為1紙質に関係熱(良好な印字品質を提供するイン
ク組成物として、米国特許4390369.44849
48.4659383号公報、特開昭55−54368
.特開昭58−108271公報に示す、常温で固体の
ホットメルト型インク組成物を用い高温下で固体状イン
クを加熱溶融させて飛翔させ、記録紙上で冷却固化し記
録ドツトを形成する方法が提案されている。
[発明が解決しようとする課題]
水等を基剤としたインク組成物においては、記録紙の紙
質により良好な印字品質を得られるものから、甚だしく
劣悪な印字品質を示すものまで印字品質の紙質依存性が
大きく5また印字後のインク乾燥時間がかかる為、実際
に両者を満足するインク組成物は実現できていない。ま
た、従来からのホットメルトインク組成物もこおいては
、記録紙への対応性、印字後の乾燥性について良好なも
のの、記録時にインク滴が記録紙紙面上において急冷固
化するため記録紙表面からインクドツトが盛り上がって
おり、また記録紙との定着強度が低く、外部からの摩擦
、熱、圧力等によるはがれ落ち、インク像の汚れ等を起
こしてしまう。
さらに急激な加熱冷却のサイクルによりインク材料が酸
化され、インク粘度が増加していく傾向にありヘッドノ
ズルからのインク吐出が不安定なるという課題を抱えて
いる。
本発明は、これら前記の課題を解決するものであり、そ
の目的とするところは、記録紙の紙質に関係なくインク
ドツト高さが低く、定着強度が良好で高い印字品質が得
られ、熱安定性の良好なインク組成物を提供することで
ある。
[課題を解決するための手段)
本発明のインク組成物は、常温より高温の状態の下でイ
ンクジェット記録装置から吐出される。
ベヒクルと色材からなるインク組成物において、酸化防
止剤を0.1〜50重量%間で含まねることを特徴とし
ている。また、ベヒクルが常温より高い融点又は流動点
を示す固体又は半固体であることを特徴としており、更
に又、ベヒクルが常;晶より高い融点又は流動点を示す
固体又は半固体及び常温で液体との混合物であることを
特徴としている。更に前記酸化防止剤はフェノール系か
ら選ばれ、その融点は50℃〜200℃間であることを
特徴としている。(ここで常温とは摂氏15℃〜30℃
の温度を言う、)
本発明のインク組成物における酸化防止剤の割合は、0
.1〜50重量%間で含まれていることが好ましいが、
更には高応答性等に適応したインクの粘度適性を考慮す
ると3,0〜40重量%間で含まれていることが好まし
い。
[作 用]
本発明のインク組成物は、均一溶液状態でインクジェッ
ト記録装置により吐出され記録紙上に印字された後、固
化するものであるが1本発明のインク組成物の一成分で
あるフェノール系の酸化防止剤は過冷却性が強く、記録
紙表面でのインクの固化時間に遅れが生じ、その表面上
でインク滴が平たくつぶれ、形成されたドツトの一部が
記録紙表面近傍の繊維中に浸透した状態で固化するため
、耐擦過性があり、且つ高密着性、高印字品質を得るこ
とができる。さらに、フェノール系酸化防止剤は、ラジ
カル連鎖禁止剤(1次酸化防止剤)として一般的にプラ
スチックやゴムの酸化防止に使用されており、その効果
は大きく1本発明のインク組成物の熱安定性も飛躍的に
向上するものである。
〔実 施 例1
以下に実施例をあげて本発明を説明する。
本発明のインク組成物は、既知の方法により調整するこ
とができ、ベヒクル成分1色材及び過冷却剤とを混合し
、ベヒクル成分の融点以上、好ましくは80℃以上に加
熱溶融後、その温度で加熱損はんした後均−溶解組成物
とし、必要に応じて高温溶融状態の下でフィルターを通
して濾過した後冷却して得ることができる6インク物性
としては動作時の温度をおよそ80℃から120°Cに
設定した場合の温度におけるインク粘度は、ヘッドの高
速応答下におけるインク供給安定性及びインク滴形成飛
翔安定性より15.0ミリパスカルセカンド(mPa、
s)以下が必要であり、更により高応答性実現の為(2
〜3 K Hz以上の応答性実現の為)には7.0mP
a、sから2.0mPa、sがより好ましい0表面張力
はノズル近傍でのメニスカス形成に影響し50dyne
/cm以下が好ましく、更にまた、印字後の記録紙玉に
おけるインクの過冷却状態におけるドツト平坦化、浸透
性促進の為に、35dyne/cm以下がより好ましい
。
常温より高い融点又は流動点を示す固体又は半固体のベ
ヒクルとして、例^ば、カルナバワックス、パラフィン
、パラフィンワックス、マイクロクリスタリンワックス
、合成ワックス、脂肪酸。
脂肪酸アミド、芳香族アミド、芳香族スルホンアミド等
から選ばれた固体状のワックス、半固体上のペトロラタ
ム、ワセリン、ラノリンワックスがあり、又常温で液体
のベヒクルとしては、液体の流動パラフィンが選ばれる
。
具体的には、
(パラフィン)
炭素数が23から32までのn−パラフィン及びイソ型
パラフィン
(パラフィンワックス)
No、115,120,125.130゜135.14
0,150.155
エイチェヌビ−(HNP)−3,9,10、エスピー(
SP)−0145,1035゜3040、3035.
01 l O
(マイクロクリスクリンワックス、その他)ハイ−ミツ
クー2045.1045、
カートワックス−3025,3735゜(以上、日本精
蝋■製)
(合成ワックス)
ステアロン、デカンジオール。
モノステアリン、ドデカンジオール
(脂肪酸)
ラウリン酸、バルミチン酸、ステアリン酸、ベヘン酸、
ブラシジン酸
(脂肪酸アミド)
エルカ酸アミド、ラウリン酸アミド、ステアリン酸アミ
ド、パルチミン酸アミド、ベヘン酸アミドブラシジン酸
アミド、オレイン酸アミド、アマイドHT−P、C(ラ
イオン掬製)脂肪酸アマイド−5,T、P、0
(花王■製)
(芳香族アミド、芳香族スルホンアミド)パラトルエン
スルホンアミド、オルトトルエンスルホンアミド
〔流動パラフィン)
ハイホワイト−70,350
(日本石油(用架)
シルコールP−55
((…松材石油研究所製)
等である。また、これらは場合によっては二種類以上を
混合しても良い。
又、フェノール系酸化防止剤としては、印字物としての
車中等の高温環境下におけるインクのにじみ、積層物と
のはりつき等を避けるための保存性等を考慮すると、最
低50℃以上の融点を有するものが選択される。融点の
最高温度はヘッドの加熱状況から200℃以下が望まし
く、さらに望ましくは150℃以下である。
具体的には、
モノフェノール系
スミライザーBHT (m、p、69℃)(2,6−ジ
ーt−ブチル−P−クレゾール)(注入化学fm製)
オリエントBHA (m、 p、57°C)(ブチル
化ヒドロキシアニゾール)
(オリエント化学掬製)
イルガノックス1107
6(、p、50〜53℃)
(オクタデシル−3−(3,5−ジ−t−ブチル−4−
ビトロキシフェニル)プロピオネート)
(チバ ガイギー社製)
ビスフェノール系
アンテージW−400
(m、p、120℃)
(2,2’−メチレン−ビス−(4−メチル−6−t−
ブチルフェノール))
(川口化学■製)
アンテージW−500
(m、p、119℃)
(2,2°−メチレン−ビス−(4−エチル−6−t−
ブチルフェノール))
(川口化学■製)
スミライザーWX (m、p、150℃)(4,4’−
チオビス−(3−メチル−6−t−ブチルフェノール)
)
(注入化学■製)
高分子フェノール系
イルガノックス1222
(m、p、50〜53℃)
(オクタデシル−3−(3,5−ジ−t−ブチル−4−
ビトロキシフェニル)プロピオネート))
(チバ ガイギー社製)
ドパノールCA
(m、p、 185〜188℃)
(1,1,3−トリス−(2−メチル−4−ヒドロキシ
−5−t−ブチルフェニル)ブタン)
(1,C,1,社製)
等である。また、これらは場合によっては二種類以上混
合しても良い。
又、色材としては耐熱性、耐水性を有した油溶染料が選
ばれる。
具体的には。
[ブラック染料]
C,1,ソルベントブラック3,22.23C,!、ア
シッドブラック123
ニグロシン
スミプラストブラック−G (BKG)、’3B(Su
miplast Black GiBKGl、3BAl
(注入化学工業■製)
スミゾールブラック−ARゾル
(Sumisol Black ARsol、l (
同上)ジエイアイブラック DT
(J、1.Black DT) (同上)[イエロー染
料]
C,1,ソルベントイエロー
19.21.61.80
アイゼンスピロ〕/イエローG RHスペシャルfAi
zen 5pilon Yeilow GR)l 5p
ecfal)(採土ケ谷化学工業■製)
スミプラストイエロー−GG、FC
(S+l11iplast Yellow GG、
PCI(注入化学工業(株)製)
[レッド、マゼンタ染料]
c、r、 ソルベントレッド
8.49.81.82.83.84゜
too、109.121
C,1,デイスパースレッド9
スミプラストレッド−A3.3B、FB(Sumipl
ast Red AS、3B、 FBI(注入化学工業
(用架)
アイゼンスビロンレッドー〇EHスペシャル(Aize
n 5pilon Red GE)l 5pecial
)(採土ケ谷化学工業(用架)
[ブルー、シアン染料]
C,!、ソルベントブルー
11.12.25.36.55.73
スミプラストブルー3R,BG
(Su+5iplast BLUE 3R1BGI
(注入化学工業(株)製)
スミプラストターコイズブルーB
(Su+m1plast Turquoise B
lue Bl(同上)
[補色用染料1
アイゼンスビロンバイオレットC−RHiAizen
5pilon Violet C−RHI(採土ケ谷化
学工業(#@製)
アイゼンスビロンイエローC−GNHニュー(Aize
n 5pilon Yellow C−GNHn
ewl(同上)
アイゼンメチルバイオレットベース
(Aizen Methyl Violet Ba5e
l(同上)
アイゼンクリスタルバイオレットパウダー(Aizen
Crystal Violet powderl(同
上)
アイゼンメチルバイオレットピュアスペシャル
(Aizen Methyl Violet p
ure 5peciall(同上)
アイゼンビクトリアピュアブルーBOHコンク
(Aizen Victoria pure Blue
BOHconc、1(同上)
アイゼングリーンC−G)l
(Aizen Green C−G11(同上)
アイゼンエスピーチーオレンジ 6
(Aizen S、P、T Orange 61
(同上)
等である。
色材の添加量は1000重量パーセント以下が好ましく
、ヘッドの高応答下における飛翔安定性及び粘度適正等
を考えると、より好ましくは5゜0重量パーセント以下
である。また、色合いの調整等で二種以上の染料を適宜
混合して用いることができる。
次に前記構成物からの具体例を示す。
実施例1
組成 重量%
色 材 :ソルベントブラック23 3.0ベヒ
クル :)INF−960,0
ステアリン酸アミド 7.0
酸化防止剤ニイルガノツクス1076 30.0前
記酸分の混合物を120℃で融解し、3時間加熱攪拌後
、高温溶融状態のままポアサイズ5ミクロンのテフロン
製メンブレンフィルターを用いて加圧濾過し、温度ll
O℃における粘度が7.0mPa、s表面張力が27.
5dyne/cmのインク組成物を得た。
次に、加熱溶融インク対応の公知のインクオンデマンド
型インクジェットプリンタヘッドを120℃に保ち、こ
れに実施例1において示したインク組成物を充填し、一
般上質紙、ボンド紙、PPC用紙等に対してビットイメ
ージ印字、文字印字等を行った後、後述のAl−A3の
評価を行った。又、インク熱安定性なA4で評価した。
(At)印字耐擦性:各種記録紙に対しての印字後、印
字面をティッシュペーパーで擦ることによる汚れの発生
の有無を印字後の時間経過によって評価し、
・10秒後発生無し ・・・好適(0)・20
〜30秒後発生無し ・・・適 (0)・30秒以上
経過後発生あり ・・・不適(×)によって分類し評価
したところ、紙質による差は若干あるものの全て「適」
以上であった。
(A2)印字物ブロッキング性:50°C高温下におい
て記録紙面上に白紙の記録紙を重ね、その上から加圧し
た状態で24時間放置した後、記録紙面におけるインク
のにじみ、重ねた記録紙へのインク転写の有無を調べ。
・インクにじみ、インク転写無し・・適 (0)・イン
クにじみ、インク転写あり・・不適(×)によって分類
評価したところ、放置前のドツト径はそのままでインク
にじみの発生は無く、またインクの転写も確認されなか
った。
(A3)インクドツト平坦性:記録紙上のインクドツト
の高さ測定と記録紙との密着′性を評価し、・ドツト高
さが5ミクロン以下で密着性も十分にある
・・・好適(0)・ドツト高さが5ミクロン
から10ミクロンで密着性も十分にある ・・
・適 (0)・ドツト高さが10ミクロンより高く密着
性も不十分 ・・・不適(×)に
よって分類し評価したところ、全て「適」以上であった
。3つの評価結果からドツトの再現性。
耐擦性の良好な印字物が得られた。
(A4) インク熱安定性:インクをパイレックス製ガ
ラス容器に入れ1000時間150℃に保ち粘度上昇に
よって評価した。
粘度上昇 20%まで ・・・好適(0)粘度上昇
30%まで ・・・適 (0)粘度上昇 30%
を越える ・・・不適(×)この評価において実施例1
のインクは当初粘度が7.0mPa、s (110℃)
であったものが8.3mPa、sになりなんらインク吐
出には問題はなかった。
以下実施例1と同様の方法で第1表:実施例2〜実施例
8に示す組成でインク組成物を得た。こねらはWj記ベ
ヒクルの具体例を示した物による様)7な組合わせにつ
いて酸化防止剤の添加量、fi類を変え示した物である
。この中で実施例4においては用いたベヒクルの主成分
が常温下で半固体あるいは液体の為、酸化防止剤との相
乗効果で色材成分を記録紙表面に残して選択的に紙中に
浸透する効果を示した。
実施例2〜実施例8についても実施例1と同様にAl−
A4の評価を行ったところ第2表に示す結果が得られた
。
比較例
実施例1と同様の方法で比較例1〜比較例3を第1表に
示す組成のインク組成物を調整した。
これら比較例についても実施例1と同様にA1−A4に
ついての評価を行ったところ第2表並びに以下に示す結
果が得られた。
比較例1
ベヒクル中50%を越える量の酸化防止剤を使用した為
、紙上での冷却固化が著しく悪化し、印字耐擦性(評価
AI)において、ドツトの固化に120秒以上かかり、
又ブロッキング性(評価A2)の評価では不適であった
。
比較例2
酸化防止剤を含有していないが過冷却物質が使用されて
いるため、印字状態は耐擦性、ブロッキング性、インク
ドツト平坦性は良好であるが、インク安定性(評価A−
4)においては粘度7.5mPa、sであったものが1
5mPa、s (100%)上昇し不適であった。
比較例3
酸化防止剤を含有しておらず、また、過冷却物質が使用
されていないため印字の時のインク平坦性(評価A3)
において、印字ドツトはすべて記録紙表面でのみ固化し
ており紙との定着性が不完全で、印字表面を擦ることに
より印字ドツトははがれおち不適であった。又、インク
安定性(評価A4)においては粘度8.3mPa、sで
あったものが13.6mPa、s (64%)上昇し不
適であった。
尚、本発明は前記実施例に限定されるものではない。
[発明の効果]
以上述べたように、常温より高;沼の状態の下でインク
ジェット記録装置から吐出される。ベヒクルと色材から
成るインク組成物において、フェノール類から選ばれた
酸化防止剤を0.1〜50.0重量パーセントの間で含
むことを特徴とすることにより記録紙の紙質に関係なく
定着強度が高<1i4tli!性、ドツト再現性の良い
良好な印字が得られるという効果を有し、さらにインク
の熱安定性に優れるという効果も有する。又1本発明に
使用の酸化防止剤を用いることにより色剤のベヒクル中
への溶解度を上げることができ、記録物の印字1度を高
くすることができるという格別な効果を有している。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to an ink composition used in an inkjet recording device. More specifically, the present invention relates to an ink composition that is used for inkjet recording at temperatures higher than room temperature. [Prior Art] Inkjet recording is excellent in quietness during recording and high-speed printing performance. BACKGROUND ART Liquid ink compositions based on water or the like have conventionally been used as ink compositions for inkjet recording. However, since ink is recorded by soaking into the paper, it has the disadvantage that when recording on paper where ink easily soaks, bleeding occurs, the periphery of the recorded dots becomes unclear, and the print quality deteriorates. For this reason, the heat related to paper quality (as an ink composition that provides good print quality, U.S. Patent No. 4390369.44849
Publication No. 48.4659383, JP-A-55-54368
.. Japanese Unexamined Patent Publication No. 58-108271 proposes a method of using a hot-melt ink composition that is solid at room temperature, heating and melting the solid ink at a high temperature, causing it to fly, and cooling and solidifying it on recording paper to form recording dots. has been done. [Problems to be Solved by the Invention] In ink compositions based on water or the like, the printing quality varies depending on the paper quality of the recording paper, ranging from good printing quality to extremely poor printing quality. In fact, an ink composition that satisfies both has not been realized because the dependence is large and the ink takes a long time to dry after printing. In addition, although conventional hot melt ink compositions have good compatibility with recording paper and drying properties after printing, ink droplets rapidly cool and solidify on the surface of the recording paper during recording. The ink dots are raised and have low fixation strength with the recording paper, causing them to peel off due to external friction, heat, pressure, etc., and cause the ink image to become smeared. Furthermore, rapid heating and cooling cycles tend to oxidize the ink material and increase the viscosity of the ink, resulting in the problem of unstable ink ejection from the head nozzles. The present invention is intended to solve the above-mentioned problems, and its purpose is to achieve high print quality with low ink dot height, good fixing strength, and high thermal stability regardless of the quality of the recording paper. An object of the present invention is to provide a good ink composition. [Means for Solving the Problems] The ink composition of the present invention is ejected from an inkjet recording device at a temperature higher than room temperature. The ink composition consisting of a vehicle and a coloring material is characterized in that it does not contain an antioxidant in an amount of 0.1 to 50% by weight. Further, the vehicle is characterized in that it is a solid or semi-solid that exhibits a melting point or pour point higher than normal temperature; It is characterized by being a mixture of. Further, the antioxidant is selected from the phenolic group and has a melting point of between 50°C and 200°C. (Here, normal temperature is 15℃ to 30℃
) The proportion of antioxidant in the ink composition of the present invention is 0.
.. It is preferably contained between 1 and 50% by weight,
Furthermore, in consideration of the viscosity suitability of the ink suitable for high responsiveness, it is preferable that the content is between 3.0 and 40% by weight. [Function] The ink composition of the present invention is ejected in a uniform solution state by an inkjet recording device and solidified after being printed on recording paper. The antioxidant has a strong supercooling property, which causes a delay in the solidification time of the ink on the surface of the recording paper, causing the ink droplets to flatten and collapse on the surface, and some of the formed dots to be absorbed into the fibers near the surface of the recording paper. Since it solidifies while penetrating the surface, it has scratch resistance, high adhesion, and high print quality. Furthermore, phenolic antioxidants are generally used as radical chain inhibitors (primary antioxidants) to prevent the oxidation of plastics and rubber, and their effect is largely due to their thermal stability in the ink composition of the present invention. Sexuality also improves dramatically. [Example 1] The present invention will be explained below with reference to Examples. The ink composition of the present invention can be prepared by a known method, in which a vehicle component (1) is mixed with a coloring material and a supercooling agent, heated to melt at a temperature higher than the melting point of the vehicle component, preferably 80° C. or higher, and then heated to a temperature higher than 80°C. After heat loss, the composition is made into a homogenized solution, and if necessary, it is filtered through a filter in a high-temperature molten state, and then cooled.6 Physical properties of the ink include operating temperatures ranging from approximately 80°C. The ink viscosity at a temperature of 120°C is determined to be 15.0 milliPascal seconds (mPa,
s) The following is required, and in order to achieve even higher response (2)
~7.0 mP for achieving response of 3 KHz or higher)
a, s to 2.0 mPa, s is more preferable 0 surface tension affects meniscus formation near the nozzle, and 50 dyne
/cm or less is preferable, and more preferably 35 dyne/cm or less is more preferable in order to flatten the dots in the supercooled state of the ink on the recording paper ball after printing and promote permeability. Solid or semi-solid vehicles exhibiting a melting point or pour point above normal temperature include, for example, carnauba wax, paraffin, paraffin wax, microcrystalline wax, synthetic wax, fatty acids. There are solid waxes selected from fatty acid amides, aromatic amides, aromatic sulfonamides, etc., semi-solid petrolatum, petrolatum, lanolin wax, and liquid paraffin is selected as a vehicle that is liquid at room temperature. . Specifically, (paraffin) n-paraffin and isotype paraffin (paraffin wax) with carbon numbers from 23 to 32 No. 115, 120, 125.130° 135.14
0,150.155 HNP-3,9,10, SP (
SP) -0145,1035°3040,3035. 01 l O (Microcrystalline wax, others) Hi-Mitsuku 2045.1045, Cartowax-3025, 3735° (all manufactured by Nippon Seiro ■) (Synthetic wax) Stearon, decanediol. Monostearin, dodecanediol (fatty acid), lauric acid, valmitic acid, stearic acid, behenic acid,
Brassic acid (fatty acid amide) Erucic acid amide, lauric acid amide, stearic acid amide, palmitic acid amide, behenic acid amide, brassic acid amide, oleic acid amide, Amide HT-P, C (manufactured by Lion Kiki) Fatty acid amide-5, T, P, 0 (manufactured by Kao ■) (Aromatic amide, aromatic sulfonamide) para-toluene sulfonamide, ortho-toluene sulfonamide [liquid paraffin] High White-70,350 (Nippon Oil (for commercial use) Silcol P-55 ((manufactured by Matsuzai Petroleum Research Institute), etc. In addition, two or more types of these may be mixed depending on the case. Also, as a phenolic antioxidant, it is suitable for use in high-temperature environments such as cars as printed materials. Considering storage stability to avoid ink bleeding at the bottom and sticking to the laminate, etc., a material with a melting point of at least 50°C is selected.The maximum melting point is 200°C or less depending on the heating condition of the head. is desirable, and more desirably 150°C or less.Specifically, Monophenol Sumilizer BHT (m, p, 69°C) (2,6-di-t-butyl-P-cresol) (manufactured by Injection Kagaku FM) Orient BHA (m, p, 57°C) (butylated hydroxyanisole) (manufactured by Orient Chemical Co., Ltd.) Irganox 1107 6 (, p, 50-53°C) (octadecyl-3-(3,5-di-t) -butyl-4-
Bitroxyphenyl) propionate) (manufactured by Ciba Geigy) Bisphenol-based ANTAGE W-400 (m, p, 120°C) (2,2'-methylene-bis-(4-methyl-6-t-
Butylphenol)) (manufactured by Kawaguchi Chemical ■) Antage W-500 (m, p, 119℃) (2,2°-methylene-bis-(4-ethyl-6-t-
butylphenol)) (manufactured by Kawaguchi Chemical ■) Sumilizer WX (m, p, 150℃) (4,4'-
Thiobis-(3-methyl-6-t-butylphenol)
) (manufactured by Inu Kagaku ■) Polymer phenolic Irganox 1222 (m, p, 50-53℃) (octadecyl-3-(3,5-di-t-butyl-4-
(bitroxyphenyl) propionate)) (manufactured by Ciba Geigy) Dopanol CA (m, p, 185-188°C) (1,1,3-tris-(2-methyl-4-hydroxy-5-t-butylphenyl) butane) (1, C, 1, manufactured by Co., Ltd.), etc. Moreover, two or more types of these may be mixed depending on the case. Moreover, as the coloring material, an oil-soluble dye having heat resistance and water resistance is selected. in particular. [Black Dye] C, 1, Solvent Black 3, 22.23C,! , Acid Black 123 Nigroshin Sumiplast Black-G (BKG), '3B (Su
miplast Black GiBKGl, 3BAl
(manufactured by Inu Kagaku Kogyo ■) Sumisol Black-ARsol (Sumisol Black ARsol, l (
Same as above) GAI Black DT (J, 1.Black DT) (Same as above) [Yellow dye] C, 1, Solvent Yellow 19.21.61.80 Eisen Spiro] / Yellow G RH Special fAi
zen 5pilon Yeilow GR)l 5p
ecfal) (manufactured by Odugaya Chemical Industry) Sumiplast Yellow-GG, FC (S+l11iplast Yellow GG,
PCI (manufactured by Inu Kagaku Kogyo Co., Ltd.) [Red, magenta dye] C, R, Solvent red 8.49.81.82.83.84゜too, 109.121 C, 1, Disperse red 9 Sumiplast red -A3.3B, FB (Sumipl
ast Red AS, 3B, FBI (Injection Chemical Industry (use rack) Aizensbiron Red〇EH Special (Aize
n 5pilon Red GE)l 5special
) (Odogaya Chemical Industry (use rack) [Blue, cyan dye] C,!, Solvent Blue 11.12.25.36.55.73 Sumiplast Blue 3R, BG (Su+5iplast BLUE 3R1BGI
(Manufactured by Inu Kagaku Kogyo Co., Ltd.) Sumiplast Turquoise B
lue Bl (same as above) [Complementary color dye 1 Aizen Violet C-RHiAizen
5pilon Violet C-RHI (manufactured by Odogaya Chemical Industry (#@)) Aizens Violet Yellow C-GNH New (Aize
n 5pilon Yellow C-GNHn
ewl (same as above) Aizen Methyl Violet Ba5e
l (same as above) Aizen Crystal Violet Powder (Aizen
Crystal Violet powder (same as above) Aizen Methyl Violet Pure Special (Aizen Methyl Violet p
ure 5special (same as above) Aizen Victoria pure Blue BOH conch (Aizen Victoria pure Blue
BOHconc, 1 (same as above) Aizen Green C-G11 (same as above) Aizen S, P, T Orange 61
(Same as above) etc. The amount of the coloring material added is preferably 1000% by weight or less, and more preferably 5.0% by weight or less in consideration of flight stability and appropriate viscosity under high response of the head. In addition, two or more types of dyes can be appropriately mixed and used for adjusting the color tone. Next, specific examples of the above components will be shown. Example 1 Composition Weight % Color Material: Solvent Black 23 3.0 Vehicle:) INF-960.0 Stearic acid amide 7.0 Antioxidant Nilganox 1076 30.0 The above acid mixture was melted at 120°C, After heating and stirring for an hour, the molten state was filtered under pressure using a Teflon membrane filter with a pore size of 5 microns.
The viscosity at 0°C is 7.0 mPa, and the surface tension is 27.
An ink composition of 5 dyne/cm was obtained. Next, a known ink-on-demand type inkjet printer head compatible with heat-melting ink was kept at 120°C, and the ink composition shown in Example 1 was filled into it, and the inkjet printer head was used to print on general high-quality paper, bond paper, PPC paper, etc. After performing bit image printing, character printing, etc., the Al-A3 was evaluated as described below. In addition, the ink was evaluated on A4 paper with thermal stability. (At) Printing abrasion resistance: After printing on various types of recording paper, the presence or absence of stains caused by rubbing the printed surface with tissue paper is evaluated based on the elapsed time after printing. ・No stains after 10 seconds ・・・Suitable (0)・20
-No occurrence after 30 seconds... Appropriate (0) - Occurrence after 30 seconds or more - Unsuitable (x) When classified and evaluated, all were rated as ``Appropriate'', although there were slight differences depending on the paper quality.
That was it. (A2) Printed matter blocking property: After stacking blank recording paper on top of the recording paper at a high temperature of 50°C and leaving it under pressure from above for 24 hours, the ink smeared on the recording paper surface and the stacked recording paper Check for ink transfer to. - No ink bleeding, no ink transfer - Appropriate (0) - Ink bleeding, ink transfer - Unsuitable (x) As a result of the classification and evaluation, the dot diameter before leaving was the same as before, no ink bleeding occurred, and the ink did not bleed. No transcription was confirmed either. (A3) Ink dot flatness: Measure the height of the ink dot on the recording paper and evaluate its adhesion to the recording paper.Dot height is 5 microns or less and adhesion is sufficient.
... Suitable (0) - Dot height is 5 to 10 microns and adhesion is sufficient...
- Appropriate (0) - Dot height is higher than 10 microns and adhesion is insufficient... When classified and evaluated by unsuitable (x), all were ``suitable'' or higher. Dot reproducibility based on three evaluation results. Printed matter with good abrasion resistance was obtained. (A4) Ink thermal stability: The ink was placed in a Pyrex glass container and kept at 150° C. for 1000 hours, and evaluated by the increase in viscosity. Viscosity increase up to 20%...Suitable (0) Viscosity increase up to 30%...Suitable (0) Viscosity increase 30%
Exceeding...Unsuitable (×) Example 1 in this evaluation
The initial viscosity of the ink was 7.0mPa,s (110℃)
The pressure was reduced to 8.3 mPa, s, and there was no problem with ink ejection. Ink compositions having the compositions shown in Table 1: Examples 2 to 8 were obtained in the same manner as in Example 1. The dough is based on the specific examples of the vehicles described in Wj) and shows seven combinations with different amounts of antioxidant and fi types. Among these, in Example 4, the main component of the vehicle used is semi-solid or liquid at room temperature, so due to the synergistic effect with the antioxidant, the colorant component remains on the surface of the recording paper and selectively penetrates into the paper. showed the effect of In Examples 2 to 8, Al-
When A4 was evaluated, the results shown in Table 2 were obtained. Comparative Example Ink compositions of Comparative Examples 1 to 3 having the compositions shown in Table 1 were prepared in the same manner as in Example 1. These comparative examples were also evaluated for A1-A4 in the same manner as in Example 1, and the results shown in Table 2 and below were obtained. Comparative Example 1 Since more than 50% of the antioxidant was used in the vehicle, the cooling solidification on paper deteriorated significantly, and in terms of print abrasion resistance (evaluation AI), it took more than 120 seconds for the dots to solidify.
Moreover, the evaluation of blocking property (evaluation A2) was unsuitable. Comparative Example 2 Since it does not contain an antioxidant but uses a supercooled substance, the print condition has good scratch resistance, blocking properties, and ink dot flatness, but the ink stability (rating A-
In 4), the viscosity was 7.5 mPa,s, but 1
The pressure increased by 5 mPa,s (100%), which was inappropriate. Comparative Example 3 Ink flatness during printing (evaluation A3) because it does not contain antioxidants and does not use supercooled substances
All the printed dots were solidified only on the surface of the recording paper, and the fixation to the paper was incomplete, and the printed dots peeled off when the printed surface was rubbed, which was unsuitable. In addition, regarding the ink stability (evaluation A4), the viscosity of the ink which was 8.3 mPa, s increased to 13.6 mPa, s (64%), which was unsuitable. Note that the present invention is not limited to the above embodiments. [Effects of the Invention] As described above, ink is ejected from an inkjet recording device under conditions higher than room temperature. The ink composition consisting of a vehicle and a coloring material is characterized by containing an antioxidant selected from phenols in an amount of 0.1 to 50.0 weight percent, so that the fixing strength is increased regardless of the quality of the recording paper. is high<1i4tli! It has the effect of providing good printing with good dot reproducibility and dot reproducibility, and also has the effect of providing excellent thermal stability of the ink. Furthermore, by using the antioxidant used in the present invention, it is possible to increase the solubility of the coloring agent in the vehicle, and it has the special effect of increasing the printing rate of recorded matter.
Claims (4)
吐出される、ベヒクルと色材からなるインク組成物にお
いて、酸化防止剤を0.1〜50重量%間で含むことを
特徴とするインク組成物。(1) An ink composition comprising a vehicle and a coloring material that is ejected from an inkjet recording device at a temperature higher than room temperature and containing an antioxidant in an amount of 0.1 to 50% by weight. .
体又は半固体であることを特徴とする請求項1記載のイ
ンク組成物。(2) The ink composition according to claim 1, wherein the vehicle is a solid or semisolid having a melting point or pour point higher than room temperature.
体又は半固体及び常温で液体との混合物であることを特
徴とする請求項1記載のインク組成物。(3) The ink composition according to claim 1, wherein the vehicle is a mixture of a solid or semi-solid having a melting point or pour point higher than room temperature and a liquid at room temperature.
が50℃〜200℃間であることを特徴とする請求項1
記載のインク組成物。(4) Claim 1, characterized in that the antioxidant is selected from phenolics and has a melting point between 50°C and 200°C.
The ink composition described.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1025066A JPH02206661A (en) | 1989-02-03 | 1989-02-03 | Ink composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1025066A JPH02206661A (en) | 1989-02-03 | 1989-02-03 | Ink composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02206661A true JPH02206661A (en) | 1990-08-16 |
Family
ID=12155552
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1025066A Pending JPH02206661A (en) | 1989-02-03 | 1989-02-03 | Ink composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02206661A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0337278A (en) * | 1989-06-22 | 1991-02-18 | Xerox Corp | Hot-melt ink composition |
US5607501A (en) * | 1994-07-26 | 1997-03-04 | Brother Kogyo Kabushiki Kaisha | Hot melt ink utilizable for ink jet printer |
JP2004018630A (en) * | 2002-06-14 | 2004-01-22 | Hitachi Printing Solutions Ltd | Solid ink composition and method for ink-jet recording |
JP2013010812A (en) * | 2011-06-28 | 2013-01-17 | Sakura Color Products Corp | Heat discoloring composition and heat discoloring ink composition |
-
1989
- 1989-02-03 JP JP1025066A patent/JPH02206661A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0337278A (en) * | 1989-06-22 | 1991-02-18 | Xerox Corp | Hot-melt ink composition |
US5607501A (en) * | 1994-07-26 | 1997-03-04 | Brother Kogyo Kabushiki Kaisha | Hot melt ink utilizable for ink jet printer |
JP2004018630A (en) * | 2002-06-14 | 2004-01-22 | Hitachi Printing Solutions Ltd | Solid ink composition and method for ink-jet recording |
JP2013010812A (en) * | 2011-06-28 | 2013-01-17 | Sakura Color Products Corp | Heat discoloring composition and heat discoloring ink composition |
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