JP3857065B2 - Ink composition, recording medium, ink jet recording method, and recorded matter - Google Patents

Description

【００５０】
【化７】

ヒドラジド系化合物は、インク組成物中、０．０１重量％以上１０重量％以下含まれることが好ましく、特に０．１重量％以上５重量％以下含まれることがさらに好ましい。好ましい含有量とすることにより、記録物の耐黄変性が著しく改善される。
【００５１】
本発明においては、前記一般式（１）で表される化合物とヒドラジド系化合物との重量比（前者／後者）が１：２５以上５：１以下であることが好ましく、特に１：５以上３：１以下であることがさらに好ましい。好ましい重量比とすることにより、記録物の耐黄変性が著しく改善される。
【００５２】
第三級アミン系化合物としては、一般式Ｒ^５Ｒ^６Ｒ^７Ｎ（Ｒ^５、Ｒ^６およびＲ^７はそれぞれ置換基を有していてもよいアルキル基、アリール基、またはアラルキル基である。）で表される化合物または置換基を有していてもよい環状第三級アミンが好ましい。
【００５３】
一般式Ｒ^５Ｒ^６Ｒ^７Ｎで表される化合物としては、Ｒ^５、Ｒ^６およびＲ^７がそれぞれ独立に置換されていてもよいアルキル基、アリール基、アラルキル基のものが挙げられる。具体的には、例えば、トリエタノールアミン、ジメチルエタノールアミン、ジエチルエタノールアミン、ブチルジエタノールアミン、メチルジエタノールアミン、トリイソプロパノールアミン、トリメチルアミン、トリエチルアミン、トリプロピルアミン、トリブチルアミン、トリアリルアミン、ジメチルアニリン、ジエチルアニリン、トリベンジルアミン、トリフェニルアミン、Ｎ，Ｎ−ジメチルベンジルアミン、Ｎ，Ｎ−ジメチルフェネチルアミン、Ｎ，Ｎ−ジエチルベンジルアミン、およびこれらの誘導体が挙げられる。Ｒ^５、Ｒ^６およびＲ^７がいずれもヒドロキシアルキル基である場合（特にトリエタノールアミン）に、特に記録物の耐黄変性に優れる。
【００５４】
置換基を有していてもよい環状第三級アミンとしては、例えば、１，４−ジアザビシクロ[2.2.2]オクタン（ＤＡＢＣＯ）、１，８−ジアザビシクロ[5.4.0]−７−ウンデセン（ＤＢＵ）、１，５−ジアザビシクロ[4.3.0]−５−ノネン（ＤＢＮ）、ヘキサメチレンテトラアミン（ＨＭＴＡ）、Ｎ−メチルピペリジン、Ｎ−メチルモリホリン、Ｎ−メチルピロリジン、Ｎ−メチルピロール、２−メチルピリジン、２−エチルピリジン、３−メチルピリジン、３−メチルキノリン、およびこれらの誘導体が挙げられる。ＤＡＢＣＯまたはＨＭＴＡを用いた場合に、特に記録物の耐黄変性に優れる。
【００５５】
これらの第三級アミン系化合物は、単独で使用しても併用してもいずれでもよい。
【００５６】
第三級アミン系化合物は、インク組成物中、０．０１重量％以上１０重量％以下含まれることが好ましく、特に０．１重量％以上５重量％以下含まれることがさらに好ましい。好ましい含有量とすることにより、記録物の耐黄変性が著しく改善される。
【００５７】
本発明においては、前記一般式（１）で表される化合物と第三級アミン系化合物との重量比（前者／後者）が１：２５以上５：１以下であることが好ましく、特に１：５以上３：１以下であることがさらに好ましい。好ましい重量比とすることにより、記録物の耐黄変性が著しく改善される。
【００５８】
無機塩類は、ＭＳ_２Ｏ_４、ＭＳＯ_３、ＭＳ_２Ｏ_３、ＭＰＨ_２Ｏ_２、ＭＰＨＯ_３（Ｍは、アルカリ金属またはアルカリ土類金属）で表される化合物からなる群より選ばれる少なくとも１つ以上のものが挙げられる。アルカリ金属としては、Ｋ、Ｎａ、Ｌｉが好ましく、アルカリ土類金属としては、Ｍｇ、Ｃａ、Ｂａが好ましい。特に、本発明の無機塩類は、カリウム塩またはナトリウム塩であることが好ましい。
【００５９】
無機塩の具体例としては、例えば、Ｋ_２Ｓ_２Ｏ_４、Ｎａ_２Ｓ_２Ｏ_４、Ｌｉ_２Ｓ_２Ｏ_４、ＭｇＳ_２Ｏ_４、ＣａＳ_２Ｏ_４、ＢａＳ_２Ｏ_４、Ｋ_２ＳＯ_３、Ｎａ_２ＳＯ_３、Ｌｉ_２ＳＯ_３、ＭｇＳＯ_３、ＣａＳＯ_３、ＢａＳＯ_３、Ｋ_２Ｓ_２Ｏ_３、Ｎａ_２Ｓ_２Ｏ_３、Ｌｉ_２Ｓ_２Ｏ_３、ＭｇＳ_２Ｏ_３、ＣａＳ_２Ｏ_３、ＢａＳ_２Ｏ_３、ＫＰＨ_２Ｏ_２、ＮａＰＨ_２Ｏ_２、ＬｉＰＨ_２Ｏ_２、Ｍｇ（ＰＨ_２Ｏ_２）_２、Ｃａ（ＰＨ_２Ｏ_２）_２、Ｂａ（ＰＨ_２Ｏ_２）、Ｋ_２ＰＨＯ_３、Ｎａ_２ＰＨＯ_３、_２Ｌｉ_２ＰＨＯ_３、ＭｇＰＨＯ_３、ＣａＰＨＯ_３、ＢａＰＨＯ_３が挙げられる。特に、カリウム塩またはナトリウム塩である場合に、記録物の耐黄変性が著しく改善される。
【００６０】
これらの無機塩は、単独で使用しても併用してもいずれでもよい。
【００６１】
無機塩類は、インク組成物中、０．０１重量％以上１０重量％以下含まれることが好ましく、特に０．１重量％以上５重量％以下含まれることがさらに好ましい。好ましい含有量とすることにより、記録物の耐黄変性が著しく改善される。
【００６２】
本発明においては、前記一般式（１）で表される化合物と無機塩類との重量比（前者／後者）が１：２５以上５：１以下であることが好ましく、特に１：５以上３：１以下であることがさらに好ましい。好ましい重量比とすることにより、記録物の耐黄変性が著しく改善される。
【００６３】
上記（１）で表される化合物は、水溶性基Ｗを有している下記一般式で表される化合物であることが好ましい。
【００６４】
【化８】

（式中、Ｗは−ＳＯ_２ＮＨ_２基、−ＮＨＣＯＣＨ_３基、−ＣＯＮＨ_２基、−Ｃ＝ＮＨ(ＮＨ_２)基、−ＮＨＣ＝ＮＨ(ＮＨ_２)基、−ＳＯ_３Ｈ基、硫酸エステル基、−Ｐ（Ｏ）（ＯＨ）（ＯＲ）、−Ｐ（Ｏ）(ＯＲ)_２、カルバモイル基またはこれらの塩、カルボキシル基の塩、アミノ基の塩、フェノール性水酸基の塩、ポリエチレングリコールエーテル基、−Ｃ＝ＮＨ(ＮＨ_２)の塩、−ＮＨＣ＝ＮＨ(ＮＨ_２)の塩、を表す（Ｒはアルキル基またはアリール基である）。また、Ｘは水素、オキシラジカル基、水酸基、アルキル基、アルケニル基、アルキニル基、アリール基、アシル基、スルホニル基、スルフィニル基、アルコキシ基、アリールオキシ基、またはアシルオキシ基であり、Ｒ^１、Ｒ^２、Ｒ^３およびＲ^４はそれぞれ水素またはアルキル基であり、Ｚは５〜７員環を完成させるために必要な非金属原子群である。ここで、Ｒ^１〜Ｒ^４およびＺのうち、何れか２つの基が互いに結合して５〜７員環を形成してもよい。）
一般式（１）において、Ｘで表されるアルキル基としては、例えばメチル基、エチル基、ｎ−プロピル基、ｉｓｏ−プロピル基、ｎ−ブチル基、ｔ−ブチル基、ｎ−オクチル基、ベンジル基、ヘキサデシル基等が挙げられ、アルケニル基としては、例えばアリル基、オレイル基等が挙げられ、アルキニル基としては、例えばエチニル基等が挙げられ、アリール基としては、例えばフェニル基、ナフチル基等が挙げられ、アシル基としては例えば、アセチル基、ベンゾイル基、ペンタノイル基等が挙げられ、スルホニル基としては、例えばメタンスルホニル基、ベンゼンスルホニル基、トルエンスルホニル基等が挙げられ、スルフィニル基としては、例えばメタンスルフィニル基、ベンゼンスルフィニル基等が挙げられ、アルコキシ基としては、例えばメチルオキシ基、エチルオキシ基、ｉ−プロピルオキシ基、ｎ−ブチルオキシ基、シクロヘキシルオキシ基、ｎ−オクチルオキシ基、１−オクチルオキシ基、ベンジルオキシ基等が挙げられ、アリールオキシ基としては、例えばフェノキシ基等が挙げられ、アシルオキシ基としては、例えばアセチルオキシ基、ベンゾイルオキシ基等が挙げられる。これらの基はいずれも置換基を有していてもよく、該置換基としては、スルホニル基、カルボキシル基、ヒドロキシ基等が挙げられる。特に、Ｘがオキシラジカル基であるものが好ましい。
【００６５】
前記一般式（１）において、Ｒ^１、Ｒ^２、Ｒ^３およびＲ^４は、前述の通り水素またはアルキル基を表す。該アルキル基は、前記Ｘで表されるアルキル基と同様の範疇から選ばれる。特にメチル基であるものが好ましい。
【００６６】
前記一般式（１）で表される化合物において、Ｚが６員環を完成させるために必要な非金属原子群であるものが好ましい。
【００６７】
以下に、一般式（１）で表される化合物のうち、６０℃、１時間放置での重量減少が１重量％以内であるものの具体例を示す。
【００６８】
【化９】

前記一般式（１）で表される化合物は、Journal of Polymer Science:PartB:Polymer Phisics;Vol.25.1299-1310(1987); written by Kunihiro Hamada,Toshiro Iijima and Ralph McGregor、Polymer;Vol.29(1).93-98(1988);written by Kunihiro Hamada,Toshiro Iijima and Ralph McGregor、等に記載の方法に準じて製造することができる。具体的には、式（１−１）の化合物は上記の前者、式（１−２）の化合物は後者の文献に記載されている製造方法により、製造することができる。
【００６９】
一方、一般式（１）で表される化合物のうち、６０℃、１時間放置での重量減少が１重量％以内ではないものの具体例としては、以下のものが挙げられる。
【００７０】
【化１０】

本発明においては、一般式（１）で表される化合物は、インク組成物中、０．０５重量％以上１０重量％以下含まれることが好ましく、特に０．１重量％以上５重量％以下含まれることがさらに好ましい。
【００７１】
着色剤としては、染料や顔料を用いることができる。 染料としては、水溶性のものが好ましく、具体的にはカラーインデックスにおいて酸性染料、直接染料、触媒染料、反応染料、可溶性建染染料、硫化染料や食用染料に分類されているもの等が挙げられる。また、カラーインデックスに記載されていないものであっても、好適に使用できるものは多い。 これらの具体例としては、C.I.ダイレクトブラック１７、１９、３２、３８、５１、６２、７１、７４、７５、１１２、１１７、１５４、１６３、１６８、C.I.アシッドブラック７、２４、２６、４８、５２、５８、６０、１０７、１０９、１１８、１１９、１３１、１４０、１５５、１５６、１８７、C.I.フードブラック１、２、C.I.リアクティヴブラック５、C.I.ダイレクトイエロー１１、２８、３３、３９、４４、５８、８６、１００、１３２、１４２、３３０、C.I.アシッドイエロー３、１９、２３、２５、２９、３８、４９、５９、６２、７２、C.I.ベーシックイエロー１１、５１、C.I.ディスパースイエロー３、５、C.I.リアクティヴイエロー２、C.I.ダイレクトレッド２３、７９、８０、８３、９９、２２０、２２４、２２７、C.I.アシッドレッド１、８、１７、１８、３２、３５、３７、４２、５２、５７、９２、１１５、１１９、１３１、１３３、１３４、１５４、１８６、２４９、２５４、２５６、C.I.ベーシックレッド１４、３９、C.I.ディスパースレッド６０、C.I.ダイレクトブルー６、８、１５、２５、７１、７６、８０、８６、９０、１０６、１０８、１２３、１６３、１６５、１６８、１９９、２２６、C.I.アシッドブルー９、２９、４０、６２、７４、１０２、１０４、１１３、１１７、１２０、１７５、１８３、C.I.ベーシックブルー４１、C.I.リアクティブブルー１５、C.I.ダイレクトバイオレット４７、５１、９０、９４、C.I.アシッドバイオレット１１、３４、７５などが挙げられる。 顔料としては、特に限定されず、無機顔料および有機顔料のいずれも使用することができる。無機顔料としては、酸化チタンおよび酸化鉄に加え、コンタクト法、ファーネスト法、サーマル法などの公知の方法によって製造されたカーボンブラックを使用することができる。また、有機顔料としては、アゾ染料（アゾレーキ、不溶性アゾ顔料、縮合アゾ顔料、キレートアゾ顔料などを含む）、多環式顔料（例えば、フタロシアニン顔料、ペリレン顔料、ペリノン顔料、アントラキノン顔料、キナクリドン顔料、ジオキサジン顔料、チオインジゴ顔料、イソインドリノン顔料、キノフラロン顔料など）、染料キレート（例えば、塩基性染料型キレート、酸性染料型キレートなど）、ニトロ顔料、ニトロソ顔料、アニリンブラックなどを使用することができる。 特に黒インクとして使用されるカーボンブラックとしては、三菱化学製のNo.2300,No.900,MCF88,No.33,No.40,No.45,No.52,MA7,MA8,MA100,No2200B 等が、コロンビア社製のRaven5750,Raven5250,Raven5000,Raven3500,Raven1255,Raven700 等が、キャボット社製のRegal 400R,Regal 330R,Rega l660R,Mogul L,Monarch 700, Monarch 800, Monarch 880, Monarch 900, Monarch 1000, Monarch 1100, Monarch 1300, Monarch 1400 等が、デグッサ社製の Color Black FW1,Color Black FW2, Color Black FW2V, Color Black FW18, Color Black FW200, Color Black S150, Color Black S160, Color Black S170, Printex 35, Printex U, Printex V, Printex 140U, Special Black 6, Special Black 5, Special Black 4A, Special Black 4 等が使用できる。 イエローインクに使用される顔料としては、C.I.Pigment Yellow 1, C.I.Pigment Yellow 2, C.I.Pigment Yellow 3, C.I.Pigment Yellow 12, C.I.Pigment Yellow 13, C.I.Pigment Yellow 14C, C.I.Pigment Yellow 16 ,C.I.Pigment Yellow 17, C.I.Pigment Yellow 73, C.I.Pigment Yellow 74, C.I.Pigment Yellow 75, C.I.Pigment Yellow 83, C.I.Pigment Yellow 93, C.I.Pigment Yellow95, C.I.Pigment Yellow97, C.I.Pigment Yellow 98, C.I.Pigment Yellow 119, C.I.Pigment Yellow 110, C.I.Pigment Yellow114, C.I.Pigment Yellow128, C.I.Pigment Yellow129, C.I.Pigment Yellow 138, C.I.Pigment Yellow 150, C.I.Pigment Yellow 151,C.I.Pigment Yellow154, C.I.Pigment Yellow155, C.I.Pigment Yellow 180, C.I.Pigment Yellow 185,等が挙げられる。 また、マゼンタインクに使用される顔料としては、C.I.Pigment Red 5, C.I.Pigment Red 7, C.I.Pigment Red 12, C.I.Pigment Red 48(Ca), C.I.Pigment Red 48(Mn), C.I.Pigment Red 57(Ca), C.I.Pigment Red 57:1, C.I.Pigment Red 112, C.I.Pigment Red 122, C.I.Pigment Red 123, C.I.Pigment Red 168, C.I.Pigment Red 184, C.I.Pigment Red 202 等が挙げられる。さらに、シアンインクに使用される顔料としては、C.I.Pigment Blue 1, C.I.Pigment Blue 2, C.I.Pigment Blue 3, C.I.Pigment Blue 15:3, C.I.Pigment Blue 15:34, C.I.Pigment Blue 15:4, C.I.Pigment Blue 16, C.I.Pigment Blue 22, C.I.Pigment Blue 60, C.I.Vat Blue 4 , C.I.Vat Blue 60が挙げられる。
着色剤の添加量はインク組成物中、好ましくは０．１重量％以上２０重量％以下が好ましく、０．５重量％以上１０重量％以下がさらに好ましい。また、顔料の場合には粒径は１０μｍ以下が好ましく、さらに好ましくは０．１μｍ以下である。
本発明のインク組成物においては、溶媒として水を用いる。水としては、イオン交換水、限外濾過水、逆浸透水、蒸留水等の純水、または超純水の何れも好ましく用いることができる。
【００７２】
本発明のインク組成物は、さらに浸透剤および／または保湿剤を含んでいてもよい。
【００７３】
浸透剤としては、インクの表面張力を低下させ記録媒体へのインクの浸透を促進しインク乾燥時間を短縮し得る化合物を広く使用できる。例えば、エタノール、プロパノール、イソプロパノール、ブタノール、ペンタノール等の低級アルコール類、エチレングリコールモノエチルエーテル、エチレングリコールモノブチルエーテル等のセロソルブ類、ジエチレングリコールモノブチルエーテル、トリエチレングリコールモノブチルエーテルグリコールエーテル等のカルビトール類、ノニオン性界面活性剤が挙げられる。
【００７４】
保湿剤としては、水分の蒸発を抑制してインクを保湿し吐出安定性を向上させ得る化合物を広く使用できる。例えば、エチレングリコール、プロピレングリコール、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、ポリプロピレングリコール、グリセリン、ジグリセリン、１，３−プロパンジオール、１，５−ペンタンジオール等の多価アルコール、マルチトール、マルトース、ソルビトール等の糖類、トリメチロールエタン、トリメチロールプロパン等のグリセリン誘導体、炭酸エチレン等の炭酸エステル類、イミダゾール、２−メチルイミダゾール等のイミダゾール誘導体、２−ピリジノール、３−ピリジノール等のピリジノール誘導体、尿素等が挙げられる。
本発明のインク組成物は、必要に応じてインクジェット記録用インクに一般的に用いられている助剤をさらに含むことができる。そのような助剤としては、ｐＨ調整剤、キレート剤、防腐剤、防錆剤等が挙げられる。 上記構成とすることにより、フェノール系誘導体の二量体化およびキノン化を防ぐことができるので、耐光性および耐目詰まり性に優れるとともに、耐黄変性に優れた記録物を得ることができる。 また本発明においては、一般式（１）で表され、６０℃、１時間放置での重量減少が１重量％以内である化合物と、ヒドラジド系化合物、第三級アミン系化合物または特定の無機塩類とを、インク組成物とは別に、または更に加えて、付与液として、記録媒体上に印加した場合においても、有効に作用する。この場合、付与液としては、色材を除き、上述のインク組成物の構成と同様の範囲で作成されることが望ましい。 次に、本発明による記録媒体の好ましい実施形態について説明する。 インク受理層としては、カラー画像や写真画像等を高画質に再現できるものとして、インク吸収顔料、インク定着剤およびバインダーから少なくとも構成されるものが知られているが、本発明の実施形態による記録媒体のインク受容層は、さらに、一般式（１）で表され６０℃、１時間放置での重量減少が１重量％以内である化合物と、ヒドラジド系化合物、第三級アミン系化合物または特定の無機塩類と、を含有するものである。 一般式（１）で表される化合物、ヒドラジド系化合物、第三級アミン系化合物、無機塩類としては、それぞれ、前述のインク組成物に用いるものと同様のものを用いるのが好ましい。 一般式（１）で表される化合物は、インク受容層の全乾燥重量中、０．０１重量％以上１０重量％以下で含まれることが好ましく、特に、０．１重量％以上５重量％以下で含まれることがさらに好ましい。 ヒドラジド系化合物、第三級アミン系化合物、無機塩類は、それぞれ、インク受容層の全乾燥重量中、０．０１重量％以上１０重量％以下で含まれることが好ましく、特に０．１重量％以上５重量％以下で含まれることがさらに好ましい。好ましい範囲とすることにより、記録物の耐黄変性が著しく改善される。 本発明においては、前記一般式（１）で表される化合物とヒドラジド系化合物、第三級アミン系化合物または無機塩類の重量比（前者／後者）は、それぞれ、１：２５以上５：１以下であることが好ましく、特に１：５以上３：１以下であることがさらに好ましい。好ましい重量範囲とすることにより、記録物の耐黄変性が著しく改善される。 インク吸収顔料としては、公知の白色顔料を１種以上用いることができ、合成非晶質シリカ、コロイダルシリカ等のシリカ、コロイダルアルミナを例示できる。 また、白色顔料としては、シリカ、アルミナの他にも、軽質炭酸カルシウム、重質炭酸カルシウム、炭酸マグネシウム、カオリン、タルク、硫酸カルシウム、硫酸バリウム、二酸化チタン、酸化亜鉛、硫化亜鉛、炭酸亜鉛、チタンホワイト、ケイ酸アルミニウム、ケイソウ土、ケイ酸カルシウム、ケイ酸マグネシウム、擬ベーマイト、水酸化アルミニウム、水酸化マグネシウム、リトポン、ゼオライト、加水ハロイサイト等の白色無機顔料、スチレン系プラスチックピグメント、アクリル系プラスチックピグメント、ポリエチレン、メラミン樹脂、尿素樹脂等の有機顔料等が挙げられる。 これらインク吸収顔料は、インク受容層の全乾燥重量中、３０重量％以上９０重量％以下で含まれることが好ましく、特に４０重量％以上８０重量％以下で含まれることがさらに好ましい。
インク定着剤としては、特にカチオン性化合物が好ましく、１級〜３級アミンあるいは４級アンモニウム塩基を有する低分子化合物、それらの基を有するオリゴマー、またはそれらの基を有するポリマーが挙げられる。具体例としては、ジアリルジメチルアンモニウムクロライドポリマー、ジアリルジメチルアンモニウムクロライド−二酸化イオウコポリマー、ジアリルジメチルアンモニウムクロライド−アクリルアミドコポリマー等のジアリルジメチルアンモニウム塩ポリマー、ジアリルアミン塩酸塩−二酸化イオウコポリマー、ジアリルメチルアミン塩酸塩コポリマー、ポリアリルアミン、ポリエチレンイミン、ポリエチレンイミン４級アンモニウム塩化合物、（メタ）アクリル酸アルキルアンモニウム塩ポリマー、（メタ）アクリルアミドアルキルアンモニウム塩ポリマー、４級アンモニウム塩を含むアイオネン、ポリアルキレンアミンジシアンジアミドアンモニウム塩縮合物等を挙げることができる。 これらインク定着剤は、インク受容層の全乾燥重量中、１重量％以上３０重量％以下で含まれることが好ましく、特に５重量％以上１０重量％以下で含まれることがさらに好ましい。 バインダーとしては、酸化デンプン、エーテル化デンプン、リン酸エステル化デンプン等のデンプン誘導体、カルボキシメチルセルロース、ヒドロキシエチルセルロース等のセルロース誘導体、カゼイン、ゼラチン、大豆蛋白、ポリビニルアルコール又はその誘導体、ポリビニルピロリドン、無水マレイン酸樹脂、スチレン−ブタジエン共重合体、メチルメタクリレート−ブタジエン共重合体等の共役ジエン系共重合体ラテックス、アクリル酸エステルおよびメタクリル酸エステルの共重合体または共重合体のアクリル系重合体等のアクリル系重合体ラテックス、エチレン酢酸ビニル共重合体等のビニル系重合ラテックス、あるいはこれら各種重合体のカルボキシル基等の官能基含有単量体による官能基変性重合体ラテックス、メラミン樹脂、尿素樹脂等の熱硬化性樹脂等の水性接着剤、ポリメチルメタクリレート等のアクリル酸エステル、メタクリル酸エステルの重合体又は共重合体、ポリウレタン樹脂、不飽和ポリエステル樹脂、塩化ビニル酢酸ビニルコポリマー、ポリビニルブチラール、アルキッド樹脂等の合成樹脂系接着剤等を挙げることができる。
これらバインダーは、インク受容層の全乾燥重量中、１０重量％以上６０重量％以下で含まれるのが好ましく、特に２０重量％以上５０重量％以下で含まれることがさらに好ましい。 また、インク受容層には、必要に応じてさらに、公知の染料固着剤（耐水化剤）、蛍光増白剤、界面活性剤、消泡剤、ｐＨ調整剤、防カビ剤、紫外線吸収剤および酸化防止剤等の各種添加剤が含有されてもよい。
以上、インク受容層の構成について説明したが、インク受容層としては、シリカまたはアルミナを主要構成成分とし、これらシリカやアルミナの粒径や、その他の構成成分の含有量等を調整することによって、インク受容層の空隙率を３０％以上８０％以下とするのが特に好ましい。空隙率を３０％以上にすることにより、特にインクの記録媒体に対する吸収性を確実に確保でき、８０％以下とすることにより、インク受容層に対し確実に強度を付与することができる。 基材としては、紙またはプラスティック製のシート状のものが使用され、光透過性のもの、光不透過性のもののいずれも使用することができる。 これら基材としては、従来公知のものを使用することができ、具体的には、紙としては、天然セルロース繊維を主体とした木材パルプまたは非木材パルプのパルプ原料からなるものが挙げられ、プラスティック材料としては、ポリエステル系樹脂、ジアセテート系樹脂、トリアセテート系樹脂、アクリル系樹脂、ポリカーボネート系樹脂、ポリ塩化ビニル系樹脂、ポリイミド系樹脂、セロハン、セルロイド等が挙げられる。 本発明の記録媒体は、上記各構成成分が、水等の適当な溶媒に溶解または分散された塗工液を、ロールコーティング法、スプレーコーティング法、ロッドバーコーティング法、エアナイフコーティング法等の公知のコーティング法により、上述の基材に塗工し、引き続き乾燥させることによって好適に得ることができる。塗工後の乾燥は、一般的な乾燥機を用いて行うことができ、一般的には１００℃〜１５０℃の範囲で行われる。 上記構成とすることにより、画像の保存性、耐光性に優れ、なおかつ耐黄変性に優れた記録物を得ることができる。 さらに、本発明のインクジェット記録方法について、説明する。本発明のインクジェット記録方法では、前記インク組成物、および／または記録媒体を用いてインクジェット記録を行うことにより、耐光性に優れ、かつ耐黄変性にも優れた記録物を得ることができる。 さらにまた、本発明のインクジェット記録方法では、インク組成物中に着色剤と、水と、一般式（１）で表され、６０℃、１時間放置での重量減少が１重量％以内である化合物とを含み、記録媒体中にヒドラジド系化合物、第三級アミン系化合物または特定の無機塩類を含んでいる場合においても、十分な耐光性を有し、かつ耐黄変性に優れた記録物を得ることができる。
【実施例】
次に、本発明を実施例によりさらに具体的に説明するが、本発明はこれらの例によって何等限定されるものではない。
【００７５】
（インク組成物の調製）
表１および２に示すような組成を有する各成分を常温にて３０分攪拌した後、１μｍのメンブランフィルターで濾過して、各インク組成物を得た。
【００７６】
（重量減少の測定）
表１および２に示す各インク組成物について、以下の方法により、一般式（１）で表される化合物の重量減少を測定した。
【００７７】
重量減少の測定方法；重量減少の測定方法としては、熱天秤を使用する方法が一般的で簡易である。熱天秤の使用時における雰囲気としては窒素または乾燥空気を使用した。室温から温度を上げてゆき、６０℃で１時間保持した。加熱速度としては１〜１０℃／分が一般的であり、本実施例においては、乾燥空気環境下、加熱速度５℃／分にて測定した。
【００７８】
【表１】

【００７９】
【表２】

（耐光性試験）
上記のインク組成物それぞれを、インクジェットプリンタＰＭ８００Ｃ（セイコーエプソン株式会社製）を用いて、これの専用カートリッジに充填して、インクジェット専用記録媒体（セイコーエプソン株式会社製、ＰＭ写真用紙）に印刷した。これを直射光のない常温常湿環境にて１日放置した後、得られた記録物の耐光性を以下の条件下で評価した。
【００８０】
まず、光照射はキセノンウエザオメーターＣｉ５０００（ＡＴＬＡＳ社製）を使用して行い、ブラックパネル３５℃、相対湿度６０％、３４０ｎｍ紫外光放射度０．１８Ｗ／ｍ^２で印刷物を曝露した。照射条件は１８０ｋＪ／ｍ^２（上記の条件下で２７８時間光照射）または３６０ｋＪ／ｍ^２（上記の条件下で５５６時間光照射）とした。
【００８１】
照射後、記録物の各色成分の反射濃度を分光光度計ＧＲＥＴＡＧ ＳＰＭ（ＧＲＥＴＡＧ社製）を用いて測定した。その際の条件は、光源Ｄ５０、光源フィルタなしで、白色標準は絶対白とし、視野角は２°とした。濃度残存率を次の基準で評価した。
【００８２】
評価Ａ：初期値の９０％を超える。
【００８３】
評価Ｂ：初期値の８０％以上９０％未満である。
【００８４】
評価Ｃ：初期値の８０％未満である。
【００８５】
（目詰まり放置試験）
インク組成物を充填したインクカートリッジを、上述のプリンタに装填し、初期的に正常にインク組成物が吐出されることを確認した後、プリンタの電源を切り、インクカートリッジを装填した状態のまま、温度４０℃、湿度２０％ＲＨの環境下に１ヵ月〜１２ヵ月放置した。所定時間放置後、プリンタを常温環境下に移し、本体温度が常温に下がるまで待ってから電源を入れ、再び印刷を行い、放置前と同等の印刷品質が得られるまでに要した復帰動作の回数を調べた。評価は下記の基準に従って行った。 評価Ａ：０〜２回の復帰動作で初期と同等の印字品質が得られた。 評価Ｂ：３〜５回の復帰動作で初期と同等の印字品質が得られた。 評価Ｃ：６回以上の復帰動作で初期と同等の印字品質が得られなかった。
【００８６】
（耐黄変性試験）
耐光性試験と同様の方法で、インクジェット専用記録媒体（ＰＭ写真用紙、セイコーエプソン株式会社製、商品名）に印刷したものを得た。
【００８７】
次いで、得られた印刷物をクリアファイル（三菱鉛筆株式会社製、商品名：ＣＬ−Ａ４２０）に入れ、温度６０℃、湿度２０％ＲＨの環境下に３日〜１ヵ月放置した。所定時間放置後、印刷物をクリアファイルより取り出し、非印字部の色変化および印刷部位およびその周辺の変色を目視にて次の基準で確認した。
【００８８】
評価Ａ：全く黄色変化せず、良好。
【００８９】
評価Ｂ：わすかに黄変しているように見えるが、画質的に問題無い程度。
【００９０】
評価Ｃ：印刷部位およびその周辺が黄色化している。
【００９１】
（印刷評価試験結果）
上記インク組成物１〜２４を用いて行った各試験の結果を表３及び表４に示す。
【００９２】
【表３】

【００９３】
【表４】

表３及び表４から分かるように、実施例１〜１６においては、比較例１〜８が、耐光性、耐目詰まり性および耐ファイル黄変性の全てを満足することができなかったのに対し、全てについて十分満足する結果が得られた。
【００９４】
（記録媒体の作製）
基材を秤量１００ｇ／ｍ^２の上質紙とし、この上質紙に、表５に示すインク受容層成分と水とを混合して得た塗工液（インク受容層成分の重量：水の重量＝２０：８０）を１５ｇ／ｍ^２となるように塗工した。塗工後、乾燥機を用いて１３０℃、２分間の間層を行い、ア〜タの記録媒体を作製した。
【００９５】
【表５】

（印刷評価試験結果）
上記の各インク組成物と各記録媒体とを、表６及び表７に示すように組み合せて印刷し、上記と同様の方法によって耐光性試験および耐黄変性試験を行った。各試験の結果を表６及び表７に示す。
【００９６】
【表６】

【００９７】
【表７】

表６及び表７から分かるように、比較例９〜１８においては耐光性、耐目詰まり性および耐ファイル黄変性の全てを満足することができなかったのに対し、実施例１７〜２７においては全てについて十分満足する結果が得られた。
【００９８】
【発明の効果】
本発明のインク組成物および記録媒体、また本発明のインクジェット記録方法によれば、記録物の耐光性に優れ、目詰まりすることがなく、さらに記録物の耐黄変性に優れた高画質な画像を得ることができる。
【００９９】
また、本発明の記録物は、記録画像の耐光性に優れ、かつ、耐黄変性に優れたものである。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to an ink composition, a recording medium, an ink jet recording method, and a recorded matter, and in particular, excellent in light stability (light resistance) of the recorded matter, without causing ink clogging, and yellowing resistance of the recorded matter. The present invention relates to an ink composition, a recording medium, a recorded matter, and an ink jet recording method that are excellent in quality and can obtain a high-quality image.
[0002]
[Prior art]
The ink jet recording method is a printing method in which recording is performed by causing droplets of an ink composition to fly and adhere to a recording medium such as paper. This method has a feature that a high-resolution and high-quality image can be printed at a high speed with a relatively inexpensive apparatus.
Conventionally, various ink compositions for use in recording by this ink jet recording method have been proposed.
[0003]
In recent years, there has been an increasing demand for improving the weather resistance (particularly light resistance) of recorded images, and for this reason, a device for incorporating a light stabilizer such as a hindered amine compound into an ink composition has been devised.
[0004]
For example, dyes and pigments 19 [Dyes and Pigments 19] (1992) 235-247 include 2,2,6,6-tetramethyl-4-hydroxypiperidine-, which is a hindered amine light stabilizer, in an aqueous solution containing a dye. It is described that the photodegradation of the dye can be prevented by adding 1-oxyl. Japanese Patent Application Laid-Open No. 11-170686, filed after the publication of the above-mentioned document (Dye and Pigment 19), discloses a specific compound (the above-mentioned 2, 2, 6) in an aqueous inkjet recording liquid containing a water-soluble dye. , 6-tetramethyl-4-hydroxypiperidine-1-oxyl or a derivative thereof) to stabilize the water-soluble dye. The compound captures radicals such as R.multidot. (Alkyl radicals) generated by photoexcitation of carbonyl compounds and the like, and ROO.multidot. (Peroxide radical) generated by the reaction between R. and oxygen in the air. It functions to stop the photo-oxidation reaction of the material and prevent photodegradation, and the printed matter recorded by ink jetting using the recording liquid is excellent in light resistance.
[Problems to be solved by the invention]
However, recording with the ink composition containing the light stabilizer described above improves the light resistance of the recorded image, but on the other hand, a film containing an antioxidant composed of a specific phenol derivative. When the recorded matter is stored in a file having the above or when the film is attached to the recorded matter, there is a new problem that the recorded matter turns yellow due to the influence of the light stabilizer.
[0005]
This is considered to be caused by the reaction of a specific phenol derivative by the action of a light stabilizer such as a hindered amine compound contained in the ink composition fixed on the recording medium. Specific examples of the phenol derivative include BHT (2,6-di-t-butyl-4-methylphenol).
[0006]
That is, since the phenolic derivative contained in the film has sublimation properties, it is transferred from the film to the recorded matter, and the phenolic derivative is dimerized by the action of the light stabilizer in the recorded matter. In addition, it is considered that the reaction product generated through the quinonization causes yellowing of the recorded material. In particular, when the light stabilizer has an oxy radical, the reaction proceeds particularly remarkably, so that it is considered that yellowing is more likely to occur.
[0007]
In addition, even when the compound that is a light stabilizer does not have oxy radicals, oxy radicals are generated in the compound that is a light stabilizer by an oxidation reaction during the process of storing recorded matter in the air. In addition, the yellowing reaction proceeds slowly but still causes yellowing of the recorded matter.
[0008]
Accordingly, an object of the present invention is to provide an ink composition, a recording medium, and an ink jet which are excellent in light resistance of a recorded material, are not clogged, and can obtain a high-quality image with almost no yellowing of the recorded material. It is to provide a recording method and recorded matter.
[0009]
[Means for Solving the Problems]
As a result of intensive studies, the present inventor has determined that the ink composition is a colorant, water, a compound represented by the general formula (1) and having a weight loss within 1% by weight at 60 ° C. for 1 hour. The inventors have found that a recording material excellent in light resistance, clogging resistance, and yellowing resistance can be obtained by including at least one specific compound A.
[0010]
The hydrazide compound in the present invention is an ester of a corresponding carboxylic acid, an acid halide, an acid derivative such as thiocarboxylic acid, a sulfonic acid derivative such as sulfonic acid or chlorosulfonic acid, or an isocyanate or diisocyanate, -CXNHNR ⁸ R ⁹ (R ⁸ and R ⁹⁾ obtained by, for example, a condensation reaction with hydrazine compounds represented by the general formula NH ₂ NR ⁸ R ⁹ (R ⁸ and R ⁹ are hydrogen, an alkyl group or an aryl group). Is a hydrogen, alkyl group or aryl group, X is S or O) group or —SO ₂ NHNR ⁸ R ⁹ (R ⁸ and R ⁹ are hydrogen, alkyl group or aryl group) group.
[0011]
In addition, the inventor has a recording medium having a receiving layer, the compound represented by the general formula (1) in which the weight loss after standing at 60 ° C. for 1 hour is 1% by weight or less. It has been found that a recording material excellent in light resistance and yellowing resistance can be obtained by including one or more specific compounds A.
[0012]
The present invention has been made on the basis of the above findings, and includes a colorant, water, a compound represented by the general formula (1) and having a weight loss within 1 wt% at 60 ° C. for 1 hour, And an ink composition comprising one or more compounds A arbitrarily selected from the following three groups represented by I to III: And at least one kind of compound A arbitrarily selected from the following three groups represented by I to III: A recording medium having a receiving layer is provided.
[0013]
Group I: hydrazide compounds
Group II: Tertiary amine compounds
Group III: Inorganic salts represented by MS ₂ O ₄ , MSO ₃ , MS ₂ O ₃ , MPH ₂ O ₂ , MPHO ₃ (M is an alkali metal or alkaline earth metal), and these ink compositions and The present invention also provides a recorded matter obtained by using a recording medium and a recording method.
[0014]
As one of the causes of yellowing of the recorded material, as described above, the phenol derivative in the film sublimates and moves to the recorded material, and is represented by the general formula (1) added as a light stabilizer. It reacts with a compound. Here, the present invention pays attention to the fact that the compound represented by the general formula (1) also has sublimation as another cause of yellowing of the recorded matter. It has been found that yellowing of a recorded matter can be prevented by adding a specific additive to a predetermined value. In addition, if weight reduction corresponds to a predetermined value, the compound represented by General formula (1) will not be specifically limited.
[0015]
In the above, the compound represented by the general formula (1) is a water-soluble group W (W is —SO ₂ NH ₂ group, —NHCOCH ₃ group, —CONH ₂ group, —C═NH (NH ₂ ) group, —NHC═NH (NH ₂ ) group, —SO ₃ H group, sulfate ester group, —P (O) (OH) (OR), —P (O) (OR) ₂ , carbamoyl group or a salt thereof, carboxyl A salt of a group, a salt of an amino group, a salt of a phenolic hydroxyl group, a polyethylene glycol ether group, a salt of —C═NH (NH ₂ ), a salt of —NHC═NH (NH ₂ ) (R is an alkyl group or It is preferably an aryl group))).
[0016]
In the compound represented by the general formula (1), Z is preferably a nonmetallic atom group necessary for completing a 6-membered ring.
[0017]
In the compound represented by the general formula (1), X may be an oxy radical group.
[0018]
In the ink composition, in order to obtain sufficient light resistance, clogging resistance, and yellowing resistance, the compound A is preferably contained in the ink composition in an amount of 0.01 wt% to 10 wt%. More preferably, it is in the range of 0.5 wt% or more and 5 wt% or less.
[0019]
In the ink composition, in order to obtain sufficient light resistance, clogging resistance, and yellowing resistance, the content of the compound represented by the general formula (1) is 0.05% by weight or more based on the total amount of the ink. It is preferably 10% by weight or less, and more preferably in the range of 0.5% by weight to 5% by weight.
[0020]
From the viewpoint of improving yellowing resistance of the recorded matter, the weight ratio (the former / the latter) of the compound represented by the general formula (1) and the compound A is preferably 1:25 or more and 5: 1 or less. In particular, the ratio is preferably from 1: 5 to 3: 1.
[0021]
In the above, the hydrazide compound has the general formula R ⁵ CXNHNR ⁶ R ⁷ (R ⁵ is an alkyl group or aryl group, R ⁶ and R ⁷ are hydrogen, alkyl group or aryl group, X is S or O), R ⁵ SO ₂ NHNR ⁶ R ⁷ (R ⁵ is an alkyl group or an aryl group, R ⁶ and R ⁷ are hydrogen, an alkyl group or an aryl group), or a general formula R ⁵ NHCXNHNR ⁶ R ⁷ (R ⁵ is an alkyl group or an aryl group) The groups R ⁶ and R ⁷ are preferably hydrogen, an alkyl group, or an aryl group, and X is a compound represented by S or O).
[0022]
The hydrazide compound may have two or more hydrazide structures in the same molecule.
[0023]
In the above, the tertiary amine compound is R ⁵ R ⁶ R ⁷ N (R ⁵ , R ⁶ and R ⁷ are each an optionally substituted alkyl group, aryl group, or aralkyl group. .), Or a cyclic tertiary amine which may have a substituent.
[0024]
In the above, the inorganic salt is selected from the group consisting of compounds represented by MS ₂ O ₄ , MSO ₃ , MS ₂ O ₃ , MPH ₂ O ₂ , MPHO ₃ (M is an alkali metal or alkaline earth metal). At least one inorganic salt.
[0025]
The inorganic salt is preferably a potassium salt or a sodium salt.
[0026]
When the compound A selected from Group I is used as an additive, the recorded matter is excellent in light resistance, clogging resistance and yellowing resistance, and also has the effect of improving the gas resistance of the recorded matter. is there.
[0027]
The ink composition may further contain a penetrating agent and / or a humectant.
[0028]
With the above configuration, dimerization and quinoneization of the phenol derivative can be prevented, so that a recorded matter having excellent light resistance and yellowing resistance can be obtained.
[0029]
In the recording medium of the present invention, the compound A contained is 0.01% by weight with respect to the total weight of the ink receiving layer in order to ensure sufficient ink absorbability with respect to the recording medium and to obtain yellowing resistance. The content is preferably 10% by weight or less, more preferably 0.5% by weight or more and 5% by weight or less.
[0030]
In the recording medium of the present invention, the compound represented by the general formula (1) is contained in the total weight of the ink receiving layer in order to ensure sufficient ink absorbability with respect to the recording medium and to obtain yellowing resistance. The content is preferably 0.01% by weight or more and 10% by weight or less, more preferably 0.5% by weight or more and 5% by weight or less.
[0031]
In the recording medium of the present invention, the weight ratio of the compound represented by the general formula (1) to the compound A (the former) is used in order to ensure sufficient ink absorbability with respect to the recording medium and to obtain yellowing resistance. / Latter) is preferably in the range of 1:25 to 5: 1, more preferably 1: 5 to 3: 1.
[0032]
Further, the ink jet recording method of the present invention performs recording by discharging a droplet of an ink composition and attaching the droplet to a recording medium, and the ink composition is used as the ink composition. It is characterized by using.
[0033]
The ink jet recording method of the present invention performs recording by discharging a droplet of an ink composition and attaching the droplet to a recording medium. The recording medium is used as the recording medium. It is characterized by.
[0034]
The ink jet recording method of the present invention is to perform recording by discharging droplets of an ink composition and attaching the droplets to a recording medium, and using the above ink composition as the ink composition, As the recording medium, an ink receiving layer is provided on a substrate, and a recording medium containing the compound A in the ink receiving layer is used.
[0035]
The inkjet recording method of the present invention performs recording by discharging droplets of an ink composition and attaching the droplets to a recording medium. The ink composition includes a colorant, water, An ink composition containing Compound A is used, and the recording medium is used as the recording medium.
[0036]
By using these recording methods, it is possible to obtain a recorded matter having excellent light resistance and excellent yellowing resistance.
[0037]
Further, as a result of intensive studies based on these inventions, the present inventors have found that a compound represented by the general formula (1) and having a weight loss within 1% by weight at 60 ° C. for 1 hour is within 1% by weight. In the case where one or more of the specific compound A is contained in the recording medium, similarly, a recorded matter excellent in light resistance and clogging resistance and excellent in yellowing resistance can be obtained. I found out.
[0038]
That is, in the ink jet recording method of the present invention, the ink composition is a colorant, water, a compound represented by the general formula (1), and a weight loss after standing at 60 ° C. for 1 hour within 1% by weight. And the recording medium contains one or more compounds A arbitrarily selected from the three groups represented by the above I to III.
[0039]
The inkjet recording method of the present invention performs recording by discharging droplets of an ink composition and attaching the droplets to a recording medium. The ink composition includes a colorant, water, An ink composition containing a compound represented by the general formula (1) and having a weight loss within 1% by weight at 60 ° C. for 1 hour is used, and the recording medium is used as the recording medium.
[0040]
In the recording method of the present invention, in order to sufficiently secure the ink absorbability with respect to the recording medium and to obtain yellowing resistance, each of the compound A contained is in an amount of 0. The content is preferably from 01% by weight to 10% by weight, and more preferably from 0.5% by weight to 5% by weight.
[0041]
In the recording method of the present invention, in order to obtain sufficient light resistance and sufficient clogging resistance, the content of the compound represented by the general formula (1) is 0.05 to the total amount of the ink. It is preferable that the content is not less than 10% by weight and not more than 10% by weight, and more preferably not less than 0.5% and not more than 5% by weight. Moreover, it is preferable that content of the compound A is 0.01 to 10 weight%.
[0042]
By using these recording methods, it is possible to obtain a recorded matter having excellent light resistance and excellent yellowing resistance.
[0043]
DETAILED DESCRIPTION OF THE INVENTION
Hereinafter, preferred embodiments of the ink composition of the present invention will be described.
[0044]
The ink composition according to the present invention includes a colorant, water, a compound represented by the general formula (1), and the compound A, and is 60 ° C. of the compound represented by the general formula (1). The weight loss after standing for 1 hour is within 1% by weight.
[0045]
Examples of the hydrazide compound include hydrazide (acyl hydrazide), thiocarbohydrazide, and derivatives thereof.
[0046]
Specifically, R ⁵ CXNHNR ⁶ R ⁷ (R ⁵ is an alkyl group or an aryl group, R ⁶ and R ⁷ are hydrogen, an alkyl group or an aryl group, X is S or O), or a general formula R ⁵ SO ₂ NHNR ⁶ R ⁷ (R ⁵ is an alkyl group or an aryl group, R ⁶ and R ⁷ are hydrogen, an alkyl group or an aryl group) or a general formula R ⁵ NHCXNHNR ⁶ R ⁷ (R ⁵ is an alkyl group or an aryl group, R ⁶ and R ⁷ are preferably hydrogen, an alkyl group, or an aryl group, and X is a compound represented by S or O).
[0047]
Furthermore, as a hydrazide compound, when two or more hydrazide structures are present in the same molecule, the recorded matter is particularly excellent in yellowing resistance.
[0048]
Specific examples of the compound represented by the general formula R ⁵ CXNHNR ⁶ R ⁷ , the general formula R ⁵ SO ₂ NHNR ⁶ R ⁷ , or the general formula R ⁵ NHCXNHNR ⁶ R ⁷ are shown below.
[0049]
[Chemical 6]

[0050]
[Chemical 7]

The hydrazide compound is preferably contained in the ink composition in an amount of 0.01% by weight to 10% by weight, and more preferably 0.1% by weight to 5% by weight. By setting it to a preferable content, yellowing resistance of the recorded matter is remarkably improved.
[0051]
In the present invention, the weight ratio (former / latter) of the compound represented by the general formula (1) to the hydrazide compound is preferably 1:25 or more and 5: 1 or less, particularly 1: 5 or more and 3 Is more preferably 1 or less. By setting a preferred weight ratio, the yellowing resistance of the recorded matter is remarkably improved.
[0052]
The tertiary amine compound of the general formula ^{R 5 R 6 R 7 N (} R 5, R 6 and ^{R 7} are an alkyl group which may have a substituent, an aryl group or an aralkyl group,. ) Or a cyclic tertiary amine which may have a substituent.
[0053]
Examples of the compound represented by the general formula R ⁵ R ⁶ R ⁷ N include those in which R ⁵ , R ⁶ and R ⁷ may be independently substituted, an alkyl group, an aryl group and an aralkyl group. Specifically, for example, triethanolamine, dimethylethanolamine, diethylethanolamine, butyldiethanolamine, methyldiethanolamine, triisopropanolamine, trimethylamine, triethylamine, tripropylamine, tributylamine, triallylamine, dimethylaniline, diethylaniline, Examples include rebenzylamine, triphenylamine, N, N-dimethylbenzylamine, N, N-dimethylphenethylamine, N, N-diethylbenzylamine, and derivatives thereof. When all of R ⁵ , R ⁶ and R ⁷ are hydroxyalkyl groups (particularly triethanolamine), the recorded matter is particularly excellent in yellowing resistance.
[0054]
Examples of the cyclic tertiary amine which may have a substituent include 1,4-diazabicyclo [2.2.2] octane (DABCO), 1,8-diazabicyclo [5.4.0] -7-undecene (DBU). ), 1,5-diazabicyclo [4.3.0] -5-nonene (DBN), hexamethylenetetraamine (HMTA), N-methylpiperidine, N-methylmorpholine, N-methylpyrrolidine, N-methylpyrrole, 2 -Methylpyridine, 2-ethylpyridine, 3-methylpyridine, 3-methylquinoline, and derivatives thereof. When DABCO or HMTA is used, the recorded material is particularly excellent in yellowing resistance.
[0055]
These tertiary amine compounds may be used alone or in combination.
[0056]
The tertiary amine compound is preferably contained in the ink composition in an amount of 0.01% by weight to 10% by weight, and more preferably 0.1% by weight to 5% by weight. By setting it to a preferable content, yellowing resistance of the recorded matter is remarkably improved.
[0057]
In the present invention, the weight ratio of the compound represented by the general formula (1) to the tertiary amine compound (the former / the latter) is preferably 1:25 or more and 5: 1 or less, particularly 1: More preferably, it is 5 or more and 3: 1 or less. By setting a preferred weight ratio, the yellowing resistance of the recorded matter is remarkably improved.
[0058]
The inorganic salt is at least one selected from the group consisting of compounds represented by MS ₂ O ₄ , MSO ₃ , MS ₂ O ₃ , MPH ₂ O ₂ , MPHO ₃ (M is an alkali metal or alkaline earth metal). The above is mentioned. As the alkali metal, K, Na, and Li are preferable, and as the alkaline earth metal, Mg, Ca, and Ba are preferable. In particular, the inorganic salt of the present invention is preferably a potassium salt or a sodium salt.
[0059]
Specific examples of the inorganic salt include, for example, K ₂ S ₂ O ₄ , Na ₂ S ₂ O ₄ , Li ₂ S ₂ O ₄ , MgS ₂ O ₄ , CaS ₂ O ₄ , BaS ₂ O ₄ , K ₂ SO _3. , Na ₂ SO ₃ , Li ₂ SO ₃ , MgSO ₃ , CaSO ₃ , BaSO ₃ , K ₂ S ₂ O ₃ , Na ₂ S ₂ O ₃ , Li ₂ S ₂ O ₃ , MgS ₂ O ₃ , CaS ₂ O ₃ BaS ₂ O ₃ , KPH ₂ O ₂ , NaPH ₂ O ₂ , LiPH ₂ O ₂ , Mg (PH ₂ O ₂ ) ₂ , Ca (PH ₂ O ₂ ) ₂ , Ba (PH ₂ O ₂ ), K ₂ PHO _{3, Na 2 PHO 3, 2} Li 2 PHO 3, MgPHO 3, CaPHO 3, BaPHO 3 and the like. In particular, in the case of a potassium salt or a sodium salt, yellowing resistance of the recorded matter is remarkably improved.
[0060]
These inorganic salts may be used alone or in combination.
[0061]
The inorganic salt is preferably contained in the ink composition in an amount of 0.01% by weight to 10% by weight, and more preferably 0.1% by weight to 5% by weight. By setting it to a preferable content, yellowing resistance of the recorded matter is remarkably improved.
[0062]
In the present invention, the weight ratio of the compound represented by the general formula (1) to the inorganic salt (the former / the latter) is preferably 1:25 or more and 5: 1 or less, particularly 1: 5 or more and 3: More preferably, it is 1 or less. By setting a preferred weight ratio, the yellowing resistance of the recorded matter is remarkably improved.
[0063]
The compound represented by the above (1) is preferably a compound represented by the following general formula having a water-soluble group W.
[0064]
[Chemical 8]

(Wherein, W is _-SO 2 NH ₂ group, -NHCOCH ₃ group, -CONH ₂ group, -C = NH (NH ₂₎ group, -NHC = NH (NH ₂₎ group, -SO ₃ H group, sulfuric acid Ester group, —P (O) (OH) (OR), —P (O) (OR) ₂ , carbamoyl group or a salt thereof, carboxyl group salt, amino group salt, phenolic hydroxyl group salt, polyethylene glycol An ether group, a salt of —C═NH (NH ₂ ), a salt of —NHC═NH (NH ₂ ) (wherein R is an alkyl group or an aryl group), and X is hydrogen, an oxy radical group, a hydroxyl group , alkyl group, alkenyl group, alkynyl group, an aryl group, an acyl group, a sulfonyl group, a sulfinyl group, an alkoxy group, an aryloxy group or an acyloxy ^{group,, R 1, R 2,} R 3 and ^{R 4} are hydrogen also respectively An alkyl group, Z is a non-metallic atomic group necessary to complete a 5- to 7-membered ring. Here, among R ¹ to R ⁴ and Z, bonded to any two groups are mutually 5 ~ May form a 7-membered ring.)
In the general formula (1), examples of the alkyl group represented by X include a methyl group, ethyl group, n-propyl group, iso-propyl group, n-butyl group, t-butyl group, n-octyl group, and benzyl. Group, hexadecyl group and the like, examples of the alkenyl group include allyl group and oleyl group, examples of the alkynyl group include ethynyl group, and examples of the aryl group include phenyl group and naphthyl group. Examples of the acyl group include an acetyl group, a benzoyl group, and a pentanoyl group. Examples of the sulfonyl group include a methanesulfonyl group, a benzenesulfonyl group, and a toluenesulfonyl group. Examples of the sulfinyl group include For example, methanesulfinyl group, benzenesulfinyl group and the like can be mentioned, and as an alkoxy group, Examples include a methyloxy group, an ethyloxy group, an i-propyloxy group, an n-butyloxy group, a cyclohexyloxy group, an n-octyloxy group, a 1-octyloxy group, a benzyloxy group, and the like. Phenoxy group etc. are mentioned, As an acyloxy group, an acetyloxy group, a benzoyloxy group, etc. are mentioned, for example. Any of these groups may have a substituent, and examples of the substituent include a sulfonyl group, a carboxyl group, and a hydroxy group. In particular, X is preferably an oxy radical group.
[0065]
In the general formula (1), R ¹ , R ² , R ³ and R ⁴ represent hydrogen or an alkyl group as described above. The alkyl group is selected from the same category as the alkyl group represented by X. Particularly preferred is a methyl group.
[0066]
In the compound represented by the general formula (1), it is preferable that Z is a nonmetallic atom group necessary for completing a 6-membered ring.
[0067]
Specific examples of the compounds represented by the general formula (1) are shown below in which the weight loss after standing at 60 ° C. for 1 hour is within 1% by weight.
[0068]
[Chemical 9]

The compound represented by the general formula (1) is Journal of Polymer Science: Part B: Polymer Phisics; Vol. 25.1299-1310 (1987); written by Kunihiro Hamada, Toshiro Iijima and Ralph McGregor, Polymer; Vol. 29 (1 93-98 (1988); written by Kunihiro Hamada, Toshiro Iijima and Ralph McGregor, and the like. Specifically, the compound of formula (1-1) can be produced by the former method, and the compound of formula (1-2) can be produced by the production method described in the latter document.
[0069]
On the other hand, among the compounds represented by the general formula (1), specific examples of those whose weight loss after standing at 60 ° C. for 1 hour is not within 1 wt% include the following.
[0070]
[Chemical Formula 10]

In the present invention, the compound represented by the general formula (1) is preferably contained in the ink composition in an amount of 0.05% by weight to 10% by weight, particularly 0.1% by weight to 5% by weight. More preferably.
[0071]
As the colorant, dyes or pigments can be used. The dye is preferably a water-soluble dye, and specific examples include those classified in the color index as acid dyes, direct dyes, catalyst dyes, reactive dyes, soluble vat dyes, sulfur dyes and food dyes. . Moreover, even if it is not described in the color index, there are many that can be suitably used. Specific examples thereof include CI direct black 17, 19, 32, 38, 51, 62, 71, 74, 75, 112, 117, 154, 163, 168, CI acid black 7, 24, 26, 48, 52. 58, 60, 107, 109, 118, 119, 131, 140, 155, 156, 187, CI Food Black 1, 2, CI Reactive Black 5, CI Direct Yellow 11, 28, 33, 39, 44, 58, 86, 100, 132, 142, 330, CI Acid Yellow 3, 19, 23, 25, 29, 38, 49, 59, 62, 72, CI Basic Yellow 11, 51, CI Disperse Yellow 3, 5, CI Reactive Yellow 2, CI Direct Red 23, 79, 80, 83, 99, 220, 224, 227, CI Acid Red 1, 8, 1 7, 18, 32, 35, 37, 42, 52, 57, 92, 115, 119, 131, 133, 134, 154, 186, 249, 254, 256, CI basic red 14, 39, CI disperse thread 60, CI Direct Blue 6, 8, 15, 25, 71, 76, 80, 86, 90, 106, 108, 123, 163, 165, 168, 199, 226, CI Acid Blue 9, 29, 40, 62, 74, 102, 104, 113, 117, 120, 175, 183, CI basic blue 41, CI reactive blue 15, CI direct violet 47, 51, 90, 94, CI acid violet 11, 34, 75, and the like. The pigment is not particularly limited, and both inorganic pigments and organic pigments can be used. As the inorganic pigment, in addition to titanium oxide and iron oxide, carbon black produced by a known method such as a contact method, a furnace method, or a thermal method can be used. Organic pigments include azo dyes (including azo lakes, insoluble azo pigments, condensed azo pigments, chelate azo pigments), polycyclic pigments (for example, phthalocyanine pigments, perylene pigments, perinone pigments, anthraquinone pigments, quinacridone pigments, dioxazines). Pigments, thioindigo pigments, isoindolinone pigments, quinofullerone pigments, etc.), dye chelates (for example, basic dye chelates, acidic dye chelates, etc.), nitro pigments, nitroso pigments, aniline black, and the like. In particular, carbon black used as black ink includes No.2300, No.900, MCF88, No.33, No.40, No.45, No.52, MA7, MA8, MA100, No2200B manufactured by Mitsubishi Chemical, etc. Raven5750, Raven5250, Raven5000, Raven3500, Raven1255, Raven700, etc. manufactured by Columbia are Regal 400R, Regal 330R, Regal660R, Mogul L, Monarch 700, Monarch 800, Monarch 880, Monarch 900, Monarch 1000, manufactured by Cabot. , Monarch 1100, Monarch 1300, Monarch 1400, etc. are Degussa Color Black FW1, Color Black FW2, Color Black FW2V, Color Black FW18, Color Black FW200, Color Black S150, Color Black S160, Color Black S170, Printex 35 , Printex U, Printex V, Printex 140U, Special Black 6, Special Black 5, Special Black 4A, Special Black 4, etc. can be used. The pigments used in yellow ink include CIPigment Yellow 1, CIPigment Yellow 2, CIPigment Yellow 3, CIPigment Yellow 12, CIPigment Yellow 13, CIPigment Yellow 14C, CIPigment Yellow 16, CIPigment Yellow 17, CIPigment Yellow 73, CIPigment Yellow 74, CIPigment Yellow 75, CIPigment Yellow 83, CIPigment Yellow 93, CIPigment Yellow95, CIPigment Yellow97, CIPigment Yellow 98, CIPigment Yellow 119, CIPigment Yellow114, CIPigment Yellow128, CIPigment Yellow129, CIPigment Yellow 138, CIPigment Yellow 150, CIPigment Yellow 151, CIPigment Yellow 154, CIPigment Yellow 155, CIPigment Yellow 180, CIPigment Yellow 185, and the like. The pigments used in magenta ink include CIPigment Red 5, CIPigment Red 7, CIPigment Red 12, CIPigment Red 48 (Ca), CIPigment Red 48 (Mn), CIPigment Red 57 (Ca), CIPigment Red 57: 1 CIPigment Red 112, CIPigment Red 122, CIPigment Red 123, CIPigment Red 168, CIPigment Red 184, CIPigment Red 202, and the like. Furthermore, as pigments used in cyan ink, CIPigment Blue 1, CIPigment Blue 2, CIPigment Blue 3, CIPigment Blue 15: 3, CIPigment Blue 15:34, CIPigment Blue 15: 4, CIPigment Blue 16, CIPigment Blue 22, CIPigment Blue 60, CIVat Blue 4 and CIVat Blue 60 are listed.
The amount of the colorant added in the ink composition is preferably from 0.1% by weight to 20% by weight, and more preferably from 0.5% by weight to 10% by weight. In the case of a pigment, the particle size is preferably 10 μm or less, more preferably 0.1 μm or less.
In the ink composition of the present invention, water is used as a solvent. As water, any of pure water such as ion exchange water, ultrafiltration water, reverse osmosis water, distilled water, or ultrapure water can be preferably used.
[0072]
The ink composition of the present invention may further contain a penetrating agent and / or a humectant.
[0073]
As the penetrant, a wide variety of compounds can be used that can reduce the surface tension of the ink, promote the penetration of the ink into the recording medium, and shorten the ink drying time. For example, lower alcohols such as ethanol, propanol, isopropanol, butanol and pentanol, cellosolves such as ethylene glycol monoethyl ether and ethylene glycol monobutyl ether, carbitols such as diethylene glycol monobutyl ether and triethylene glycol monobutyl ether glycol ether, Nonionic surfactant is mentioned.
[0074]
As the humectant, a wide variety of compounds that can suppress the evaporation of moisture and moisturize the ink to improve the ejection stability can be used. For example, polyhydric alcohols such as ethylene glycol, propylene glycol, diethylene glycol, triethylene glycol, polyethylene glycol, polypropylene glycol, glycerin, diglycerin, 1,3-propanediol, 1,5-pentanediol, maltitol, maltose, sorbitol Saccharides such as trimethylolethane, trimethylolpropane, carbonate esters such as ethylene carbonate, imidazole derivatives such as imidazole and 2-methylimidazole, pyridinol derivatives such as 2-pyridinol and 3-pyridinol, urea, etc. Can be mentioned.
The ink composition of the present invention can further contain an auxiliary agent that is generally used for ink jet recording ink, if necessary. Examples of such auxiliary agents include pH adjusters, chelating agents, preservatives, and rust inhibitors. With the above structure, dimerization and quinonization of the phenol derivative can be prevented, and thus a recorded matter having excellent light resistance and clogging resistance and excellent yellowing resistance can be obtained. In the present invention, a compound represented by the general formula (1) and having a weight loss within 1% by weight after standing at 60 ° C. for 1 hour, a hydrazide compound, a tertiary amine compound, or a specific inorganic salt Separately or in addition to the ink composition, even when applied as an application liquid on a recording medium. In this case, it is desirable that the application liquid is prepared in the same range as the above-described ink composition except for the coloring material. Next, a preferred embodiment of the recording medium according to the present invention will be described. As the ink receiving layer, a layer composed of at least an ink absorbing pigment, an ink fixing agent, and a binder is known as a material capable of reproducing a color image, a photographic image, or the like with high image quality. The ink receiving layer of the medium further comprises a compound represented by the general formula (1) and a weight loss within 1% by weight after standing at 60 ° C. for 1 hour, a hydrazide compound, a tertiary amine compound, or a specific compound. And inorganic salts. As the compound represented by the general formula (1), the hydrazide compound, the tertiary amine compound, and the inorganic salts, it is preferable to use the same compounds as those used in the ink composition described above. The compound represented by the general formula (1) is preferably contained in an amount of 0.01% by weight or more and 10% by weight or less, particularly 0.1% by weight or more and 5% by weight or less in the total dry weight of the ink receiving layer. More preferably, it is contained. The hydrazide compound, tertiary amine compound, and inorganic salt are each preferably contained in an amount of 0.01% by weight to 10% by weight, particularly 0.1% by weight or more, based on the total dry weight of the ink receiving layer. More preferably, it is contained in an amount of 5% by weight or less. By setting it as a preferable range, yellowing resistance of the recorded matter is remarkably improved. In the present invention, the weight ratio (the former / the latter) of the compound represented by the general formula (1) and the hydrazide compound, the tertiary amine compound or the inorganic salt is 1:25 or more and 5: 1 or less, respectively. In particular, it is more preferably 1: 5 or more and 3: 1 or less. By setting the weight in a preferable range, yellowing resistance of the recorded matter is remarkably improved. As the ink absorbing pigment, one or more known white pigments can be used, and examples thereof include silica such as synthetic amorphous silica and colloidal silica, and colloidal alumina. In addition to silica and alumina, white pigments include light calcium carbonate, heavy calcium carbonate, magnesium carbonate, kaolin, talc, calcium sulfate, barium sulfate, titanium dioxide, zinc oxide, zinc sulfide, zinc carbonate, titanium. White inorganic pigments such as white, aluminum silicate, diatomaceous earth, calcium silicate, magnesium silicate, pseudo-boehmite, aluminum hydroxide, magnesium hydroxide, lithopone, zeolite, hydrous halloysite, styrene plastic pigment, acrylic plastic pigment, Examples thereof include organic pigments such as polyethylene, melamine resin, and urea resin. These ink absorbing pigments are preferably contained in an amount of 30% by weight or more and 90% by weight or less, and more preferably 40% by weight or more and 80% by weight or less, based on the total dry weight of the ink receiving layer.
As the ink fixing agent, a cationic compound is particularly preferable, and examples thereof include low molecular compounds having primary to tertiary amines or quaternary ammonium bases, oligomers having these groups, and polymers having these groups. Specific examples include diallyldimethylammonium chloride polymer, diallyldimethylammonium chloride-sulfur dioxide copolymer, diallyldimethylammonium salt polymer such as diallyldimethylammonium chloride-acrylamide copolymer, diallylamine hydrochloride-sulfur dioxide copolymer, diallylmethylamine hydrochloride copolymer, Polyallylamine, polyethyleneimine, polyethyleneimine quaternary ammonium salt compound, (meth) acrylic acid alkylammonium salt polymer, (meth) acrylamide alkylammonium salt polymer, ionene containing quaternary ammonium salt, polyalkyleneamine dicyandiamide ammonium salt condensate, etc. Can be mentioned. These ink fixing agents are preferably contained in an amount of 1% by weight to 30% by weight, and more preferably 5% by weight to 10% by weight, based on the total dry weight of the ink receiving layer. Examples of binders include starch derivatives such as oxidized starch, etherified starch and phosphate esterified starch, cellulose derivatives such as carboxymethylcellulose and hydroxyethylcellulose, casein, gelatin, soy protein, polyvinyl alcohol or derivatives thereof, polyvinylpyrrolidone, maleic anhydride Acrylics such as resins, styrene-butadiene copolymers, conjugated diene copolymer latexes such as methyl methacrylate-butadiene copolymers, copolymers of acrylic esters and methacrylic esters, or acrylic copolymers of copolymers Polymeric latex, vinyl-based polymer latex such as ethylene vinyl acetate copolymer, or functional group-modified polymer latex with functional group-containing monomers such as carboxyl groups of these polymers, melamine resin Aqueous adhesives such as thermosetting resins such as urea resins, acrylic esters such as polymethyl methacrylate, polymers or copolymers of methacrylic esters, polyurethane resins, unsaturated polyester resins, vinyl chloride vinyl acetate copolymers, polyvinyl butyral And synthetic resin adhesives such as alkyd resins.
These binders are preferably contained in the total dry weight of the ink receiving layer in an amount of 10% by weight to 60% by weight, and more preferably 20% by weight to 50% by weight. In addition, the ink receiving layer may further include a known dye fixing agent (waterproofing agent), a fluorescent brightening agent, a surfactant, an antifoaming agent, a pH adjusting agent, an antifungal agent, an ultraviolet absorber, if necessary. Various additives such as an antioxidant may be contained.
As described above, the configuration of the ink receiving layer has been described. As the ink receiving layer, silica or alumina is a main component, and by adjusting the particle size of these silica and alumina, the content of other components, and the like, The porosity of the ink receiving layer is particularly preferably 30% or more and 80% or less. By setting the porosity to 30% or more, it is possible to ensure particularly the ink absorbability to the recording medium, and by setting it to 80% or less, it is possible to reliably impart strength to the ink receiving layer. As the substrate, a paper or plastic sheet is used, and either a light-transmitting material or a light-impermeable material can be used. As these base materials, conventionally known materials can be used. Specifically, as the paper, those made of a pulp raw material of wood pulp or non-wood pulp mainly composed of natural cellulose fibers can be mentioned. Examples of the material include polyester resin, diacetate resin, triacetate resin, acrylic resin, polycarbonate resin, polyvinyl chloride resin, polyimide resin, cellophane, celluloid, and the like. In the recording medium of the present invention, a coating solution in which each of the above-mentioned constituents is dissolved or dispersed in a suitable solvent such as water is used in known methods such as roll coating, spray coating, rod bar coating, and air knife coating. It can be suitably obtained by coating the above-mentioned substrate by a coating method and subsequently drying. Drying after coating can be performed using a general dryer, and is generally performed in the range of 100 ° C to 150 ° C. With the above configuration, a recorded matter having excellent image storage stability and light resistance and excellent yellowing resistance can be obtained. Furthermore, the ink jet recording method of the present invention will be described. In the ink jet recording method of the present invention, by performing ink jet recording using the ink composition and / or the recording medium, a recorded matter having excellent light resistance and excellent yellowing resistance can be obtained. Furthermore, in the ink jet recording method of the present invention, the compound represented by the general formula (1) in the ink composition is represented by the general formula (1), and the weight loss after standing at 60 ° C. for 1 hour is within 1% by weight. Even if the recording medium contains a hydrazide compound, a tertiary amine compound or a specific inorganic salt, a recorded material having sufficient light resistance and excellent yellowing resistance can be obtained. be able to.
【Example】
EXAMPLES Next, although an Example demonstrates this invention further more concretely, this invention is not limited at all by these examples.
[0075]
(Preparation of ink composition)
Each component having the composition shown in Tables 1 and 2 was stirred at room temperature for 30 minutes, and then filtered through a 1 μm membrane filter to obtain each ink composition.
[0076]
(Measurement of weight loss)
For each ink composition shown in Tables 1 and 2, weight loss of the compound represented by the general formula (1) was measured by the following method.
[0077]
Method for measuring weight loss; As a method for measuring weight loss, a method using a thermobalance is common and simple. Nitrogen or dry air was used as the atmosphere when using the thermobalance. The temperature was raised from room temperature and held at 60 ° C. for 1 hour. The heating rate is generally 1 to 10 ° C./min. In this example, the measurement was performed at a heating rate of 5 ° C./min in a dry air environment.
[0078]
[Table 1]

[0079]
[Table 2]

(Light resistance test)
Each of the ink compositions described above was filled into a dedicated cartridge using an ink jet printer PM800C (manufactured by Seiko Epson Corporation) and printed on an ink jet recording medium (manufactured by Seiko Epson Corporation, PM photographic paper). This was left for 1 day in a room temperature and humidity environment without direct light, and then the light resistance of the obtained recorded material was evaluated under the following conditions.
[0080]
First, light irradiation was performed using a xenon weatherometer Ci5000 (manufactured by ATLAS), and the printed matter was exposed at a black panel of 35 ° C., a relative humidity of 60%, and a 340 nm ultraviolet light emission of 0.18 W / m ² . The irradiation conditions were 180 kJ / m ² (light irradiation for 278 hours under the above conditions) or 360 kJ / m ² (light irradiation for 556 hours under the above conditions).
[0081]
After the irradiation, the reflection density of each color component of the recorded matter was measured using a spectrophotometer GRETAG SPM (manufactured by GRETAG). The conditions at that time were the light source D50, no light source filter, the white standard was absolute white, and the viewing angle was 2 °. The residual concentration rate was evaluated according to the following criteria.
[0082]
Evaluation A: It exceeds 90% of the initial value.
[0083]
Evaluation B: 80% or more and less than 90% of the initial value.
[0084]
Evaluation C: Less than 80% of the initial value.
[0085]
(Clogging test)
After loading the ink cartridge filled with the ink composition into the above-mentioned printer and confirming that the ink composition is normally discharged normally initially, the printer is turned off and the ink cartridge is loaded. It was left for 1 to 12 months in an environment of a temperature of 40 ° C. and a humidity of 20% RH. After leaving the printer for a specified period of time, move the printer to room temperature, wait until the printer cools down to room temperature, turn on the power, print again, and the number of return operations required until the same print quality as before was obtained. I investigated. Evaluation was performed according to the following criteria. Evaluation A: Print quality equivalent to the initial value was obtained in 0 to 2 return operations. Evaluation B: Print quality equivalent to the initial value was obtained after 3 to 5 return operations. Evaluation C: Print quality equivalent to the initial value was not obtained after 6 or more return operations.
[0086]
(Yellowing resistance test)
In the same manner as the light resistance test, an ink jet recording medium (PM photo paper, manufactured by Seiko Epson Corporation, trade name) was obtained.
[0087]
Subsequently, the obtained printed matter was put in a clear file (trade name: CL-A420, manufactured by Mitsubishi Pencil Co., Ltd.) and left in an environment of a temperature of 60 ° C. and a humidity of 20% RH for 3 days to 1 month. After leaving for a predetermined time, the printed matter was taken out from the clear file, and the color change of the non-printing part and the discoloration of the printed part and its periphery were visually confirmed on the following criteria.
[0088]
Evaluation A: No yellow change at all and good.
[0089]
Evaluation B: Although it appears to be faintly yellowed, there is no problem in image quality.
[0090]
Evaluation C: The printing site and its periphery are yellowed.
[0091]
(Print evaluation test results)
Tables 3 and 4 show the results of tests performed using the ink compositions 1 to 24.
[0092]
[Table 3]

[0093]
[Table 4]

As can be seen from Tables 3 and 4, in Examples 1 to 16, Comparative Examples 1 to 8 could not satisfy all of light resistance, clogging resistance and file yellowing resistance. All the results were fully satisfactory.
[0094]
(Preparation of recording medium)
The base material was a high-quality paper having a weight of 100 g / m ² , and a coating liquid obtained by mixing the high-quality paper with the ink receiving layer component and water shown in Table 5 (weight of ink receiving layer component: weight of water = 20:80) was applied to 15 g / m ² . After the coating, a layer was formed at 130 ° C. for 2 minutes using a dryer to prepare an A to A recording medium.
[0095]
[Table 5]

(Print evaluation test results)
Each ink composition and each recording medium were combined and printed as shown in Tables 6 and 7, and a light resistance test and a yellowing resistance test were performed in the same manner as described above. The results of each test are shown in Tables 6 and 7.
[0096]
[Table 6]

[0097]
[Table 7]

As can be seen from Tables 6 and 7, in Comparative Examples 9 to 18, light resistance, clogging resistance and file yellowing resistance could not be satisfied, whereas in Examples 17 to 27, Satisfactory results were obtained for all.
[0098]
【The invention's effect】
According to the ink composition and the recording medium of the present invention, and the ink jet recording method of the present invention, a high-quality image having excellent light resistance of the recorded matter, without clogging, and excellent in yellowing resistance of the recorded matter. Can be obtained.
[0099]
The recorded matter of the present invention is excellent in light resistance of recorded images and excellent in yellowing resistance.

Claims (33)

Colorants, water,
A compound represented by the following general formula (1) and having a weight loss within 1% by weight after standing at 60 ° C. for 1 hour;
An ink composition comprising: one or more compounds A arbitrarily selected from the following three groups represented by I to III.
Group I: Hydrazide compounds
Group II: Tertiary amine compounds
Group III: Inorganic salts represented by MS ₂ O ₄ , MSO ₃ , MS ₂ O ₃ , MPH ₂ O ₂ , MPHO ₃ (M is an alkali metal or alkaline earth metal)

(In the formula (1), X is hydrogen, oxy radical group, hydroxyl group, alkyl group, alkenyl group, alkynyl group, aryl group, acyl group, sulfonyl group, sulfinyl group, alkoxy group, aryloxy group or acyloxy group, R ¹ , R ² , R ³ and R ⁴ are each hydrogen or an alkyl group, and Z is a group of nonmetallic atoms necessary to complete a 5- to 7-membered ring, where R ^{1 to} R ⁴ and Any two groups of Z may be bonded to each other to form a 5- to 7-membered ring.) The ink composition according to claim 1, wherein the compound represented by the general formula (1) is a compound represented by the following general formula having a water-soluble group W.

(Wherein, W is _-SO 2 NH ₂ group, -NHCOCH ₃ group, -CONH ₂ group, -C = NH (NH ₂₎ group, -NHC = NH (NH ₂₎ group, -SO ₃ H group, sulfuric acid Ester group, —P (O) (OH) (OR), —P (O) (OR) ₂ , carbamoyl group or a salt thereof, carboxyl group salt, amino group salt, phenolic hydroxyl group salt, polyethylene glycol An ether group, a salt of —C═NH (NH ₂ ), a salt of —NHC═NH (NH ₂ ) (wherein R is an alkyl group or an aryl group), and X is hydrogen, an oxy radical group, a hydroxyl group , alkyl group, alkenyl group, alkynyl group, an aryl group, an acyl group, a sulfonyl group, a sulfinyl group, an alkoxy group, an aryloxy group or an acyloxy ^{group,, R 1, R 2,} R 3 and ^{R 4} are hydrogen also respectively An alkyl group, Z is a non-metallic atomic group necessary to complete a 5- to 7-membered ring. Here, among R ¹ to R ⁴ and Z, bonded to any two groups are mutually 5 ~ May form a 7-membered ring.)   The ink composition according to claim 1 or 2, wherein in the compound represented by the general formula (1), Z is a nonmetallic atom group necessary for completing a six-membered ring.   The ink composition according to claim 1, wherein in the compound represented by the general formula (1), X is an oxy radical group.   The ink composition according to any one of claims 1 to 4, wherein the compound A is contained in an ink composition in an amount of 0.01 wt% to 10 wt%.   The ink composition according to any one of claims 1 to 5, wherein the compound represented by the general formula (1) is contained in an amount of 0.05% by weight to 10% by weight in the ink composition.   The ink according to claim 1, wherein a weight ratio (the former / the latter) of the compound represented by the general formula (1) and the compound A is 1:25 or more and 5: 1 or less. Composition.   The ink composition according to claim 1, wherein the compound A is Group I.   The ink composition according to claim 1, wherein the compound A is Group II.   The ink composition according to any one of claims 1 to 7, wherein the compound A is Group III. The hydrazide compound has the general formula R ⁵ CXNHNR ⁶ R ⁷ (R ⁵ is an alkyl group or an aryl group, R ⁶ and R ⁷ are hydrogen, an alkyl group or an aryl group, X is S or O), or a general formula R ^{5 _{SO 2 NHNR 6 R 7 (R}} 5 is an alkyl group or an aryl group, ^{R 6} and ^{R 7} are hydrogen, an alkyl group or an aryl group) is a compound represented by any one of claims 1 to 8 Ink composition. The hydrazide compound is a compound represented by the general formula R ⁵ NHCXNHNR ⁶ R ⁷ (R ⁵ is an alkyl group or aryl group, R ⁶ and R ⁷ are hydrogen, alkyl group, or aryl group, X is S or O) The ink composition according to any one of claims 1 to 8, wherein   The ink composition according to any one of claims 1 to 8, wherein the hydrazide-based compound has two or more hydrazide structures in the same molecule. The tertiary amine compound is a general formula R ⁵ R ⁶ R ⁷ N (R ⁵ , R ⁶ and R ⁷ are each an optionally substituted alkyl group, aryl group or aralkyl group. The ink composition according to claim 1, which is a compound represented by the formula:   The ink composition according to claim 1, wherein the tertiary amine compound is a cyclic tertiary amine which may have a substituent.   The ink composition according to claim 1, wherein the tertiary amine compound is 1,4-diazabicyclo [2.2.2] octane and / or hexamethylenetetraamine.   The ink composition according to claim 1, wherein the inorganic salt is a potassium salt or a sodium salt.   The ink composition according to any one of claims 1 to 17, further comprising a penetrating agent and / or a humectant. A recording medium having an ink receiving layer provided on a substrate,
In the ink-receiving layer, a compound represented by the following general formula (1) and having a weight loss within 1% by weight after standing at 60 ° C. for 1 hour, and any of the following three groups represented by I to III: A recording medium comprising one or more compounds A selected from
Group I: Hydrazide compounds
Group II: Tertiary amine compounds
Group III: Inorganic salts represented by MS ₂ O ₄ , MSO ₃ , MS ₂ O ₃ , MPH ₂ O ₂ , MPHO ₃ (M is an alkali metal or alkaline earth metal)

(In the formula (1), X is hydrogen, oxy radical group, hydroxyl group, alkyl group, alkenyl group, alkynyl group, aryl group, acyl group, sulfonyl group, sulfinyl group, alkoxy group, aryloxy group or acyloxy group, R ¹ , R ² , R ³ and R ⁴ are each hydrogen or an alkyl group, and Z is a group of nonmetallic atoms necessary to complete a 5- to 7-membered ring, where R ^{1 to} R ⁴ and Any two groups of Z may be bonded to each other to form a 5- to 7-membered ring.)   20. The recording medium according to claim 19, wherein the compound A is contained in an amount of 0.01% by weight to 10% by weight with respect to the total amount of the ink receiving layer.   The recording medium according to claim 19 or 20, wherein the compound represented by the general formula (1) is contained in an amount of 0.01 wt% to 10 wt% with respect to the total amount of the ink receiving layer.   The weight ratio (the former / the latter) of the compound represented by the general formula (1) and the compound A is in a range of 1:25 or more and 5: 1 or less, according to any one of claims 19 to 21. The recording medium described. An inkjet recording method for performing recording by discharging droplets of an ink composition and attaching the droplets to a recording medium,
An ink jet recording method comprising using the ink composition according to any one of claims 1 to 18 as the ink composition. An inkjet recording method for performing recording by discharging droplets of an ink composition and attaching the droplets to a recording medium,
An inkjet recording method using the recording medium according to any one of claims 19 to 22 as the recording medium. An ink jet recording method for performing recording by discharging a droplet of an ink composition and attaching the droplet to a recording medium, wherein the ink according to any one of claims 1 to 18 is used as the ink composition. Using the composition,
An inkjet recording method using the recording medium according to any one of claims 19 to 22 as the recording medium. An inkjet recording method for performing recording by discharging droplets of an ink composition and attaching the droplets to a recording medium,
As the ink composition, using the ink composition according to any one of claims 1 to 18,
As the recording medium, an ink receiving layer is provided on a substrate, and the ink receiving layer contains one or more kinds of compounds A arbitrarily selected from the following three groups represented by I to III. An ink jet recording method using a medium.
Group I: Hydrazide compounds
Group II: Tertiary amine compounds
Group III: Inorganic salts represented by MS ₂ O ₄ , MSO ₃ , MS ₂ O ₃ , MPH ₂ O ₂ , MPHO ₃ (M is an alkali metal or alkaline earth metal) An inkjet recording method for performing recording by discharging droplets of an ink composition and attaching the droplets to a recording medium,
As the ink composition, an ink composition comprising a colorant, water, and one or more compounds A arbitrarily selected from the following three groups represented by I to III is used.
An inkjet recording method using the recording medium according to any one of claims 19 to 22 as the recording medium.
Group I: Hydrazide compounds
Group II: Tertiary amine compounds
Group III: Inorganic salts represented by MS ₂ O ₄ , MSO ₃ , MS ₂ O ₃ , MPH ₂ O ₂ , MPHO ₃ (M is an alkali metal or alkaline earth metal) An inkjet recording method for performing recording by discharging droplets of an ink composition and attaching the droplets to a recording medium,
The ink composition includes a colorant, water, and a compound represented by the following general formula (1), wherein the weight loss after standing at 60 ° C. for 1 hour is 1% by weight or less:
Further, the recording medium is provided with an ink receiving layer on a substrate, and the ink receiving layer contains at least one kind of compound A arbitrarily selected from the following three groups represented by I to III. An ink jet recording method comprising:
Group I: Hydrazide compounds
Group II: Tertiary amine compounds
Group III: Inorganic salts represented by MS ₂ O ₄ , MSO ₃ , MS ₂ O ₃ , MPH ₂ O ₂ , MPHO ₃ (M is an alkali metal or alkaline earth metal)

(In the formula (1), X is hydrogen, oxy radical group, hydroxyl group, alkyl group, alkenyl group, alkynyl group, aryl group, acyl group, sulfonyl group, sulfinyl group, alkoxy group, aryloxy group or acyloxy group, R ¹ , R ² , R ³ and R ⁴ are each hydrogen or an alkyl group, and Z is a group of nonmetallic atoms necessary to complete a 5- to 7-membered ring, where R ^{1 to} R ⁴ and Any two groups of Z may be bonded to each other to form a 5- to 7-membered ring.) An inkjet recording method for performing recording by discharging droplets of an ink composition and attaching the droplets to a recording medium,
As the ink composition, a colorant, and water, the ink composition comprising a compound weight loss is within 1 weight percent of at represented 60 ° C. 1 hour standing by the following general formula (1) used,
An inkjet recording method using the recording medium according to any one of claims 19 to 22 as the recording medium.

(In the formula (1), X is hydrogen, oxy radical group, hydroxyl group, alkyl group, alkenyl group, alkynyl group, aryl group, acyl group, sulfonyl group, sulfinyl group, alkoxy group, aryloxy group or acyloxy group, R ¹ , R ² , R ³ and R ⁴ are each hydrogen or an alkyl group, and Z is a group of nonmetallic atoms necessary to complete a 5- to 7-membered ring, where R ^{1 to} R ⁴ and Any two groups of Z may be bonded to each other to form a 5- to 7-membered ring.)   30. The ink jet recording method according to claim 28 or 29, wherein the content of the compound represented by the general formula (1) in the ink composition is 0.05% by weight or more and 10% by weight or less.   28. The ink jet recording method according to claim 27, wherein the content of the compound A in the ink composition is 0.01% by weight or more and 10% by weight or less.   The ink jet recording method according to claim 26 or 28, wherein the content of the compound A in the recording medium is 0.01 wt% or more and 10 wt% or less.   A recorded matter recorded by the ink jet recording method according to any one of claims 23 to 32.