JPH01283184A - Color developer for leuco dye - Google Patents
Color developer for leuco dyeInfo
- Publication number
- JPH01283184A JPH01283184A JP63112951A JP11295188A JPH01283184A JP H01283184 A JPH01283184 A JP H01283184A JP 63112951 A JP63112951 A JP 63112951A JP 11295188 A JP11295188 A JP 11295188A JP H01283184 A JPH01283184 A JP H01283184A
- Authority
- JP
- Japan
- Prior art keywords
- color developer
- color
- sio2
- periodic table
- leuco dye
- 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
- 230000000737 periodic effect Effects 0.000 claims abstract description 7
- 239000000203 mixture Substances 0.000 claims abstract description 5
- 239000000975 dye Substances 0.000 claims description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 11
- 239000006185 dispersion Substances 0.000 abstract description 6
- 239000004372 Polyvinyl alcohol Substances 0.000 abstract description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 abstract description 4
- 238000000034 method Methods 0.000 abstract description 3
- 229910052681 coesite Inorganic materials 0.000 abstract 5
- 229910052906 cristobalite Inorganic materials 0.000 abstract 5
- 239000000377 silicon dioxide Substances 0.000 abstract 5
- 235000012239 silicon dioxide Nutrition 0.000 abstract 5
- 229910052682 stishovite Inorganic materials 0.000 abstract 5
- 229910052905 tridymite Inorganic materials 0.000 abstract 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 4
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 abstract 2
- 238000002845 discoloration Methods 0.000 abstract 2
- 239000002023 wood Substances 0.000 abstract 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- -1 4-hydroxydiphenoxide Chemical compound 0.000 description 4
- 238000005562 fading Methods 0.000 description 4
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- 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 3
- 239000004927 clay Substances 0.000 description 3
- 229960004889 salicylic acid Drugs 0.000 description 3
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
- NFIDBGJMFKNGGQ-UHFFFAOYSA-N 2-(2-methylpropyl)phenol Chemical group CC(C)CC1=CC=CC=C1O NFIDBGJMFKNGGQ-UHFFFAOYSA-N 0.000 description 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- OMNHTTWQSSUZHO-UHFFFAOYSA-N 4-hydroxy-3,5-dimethylbenzoic acid Chemical compound CC1=CC(C(O)=O)=CC(C)=C1O OMNHTTWQSSUZHO-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- ALLSOOQIDPLIER-UHFFFAOYSA-N 2,3,4-trichlorobenzoic acid Chemical compound OC(=O)C1=CC=C(Cl)C(Cl)=C1Cl ALLSOOQIDPLIER-UHFFFAOYSA-N 0.000 description 1
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 description 1
- XGAYQDWZIPRBPF-UHFFFAOYSA-N 2-hydroxy-3-propan-2-ylbenzoic acid Chemical compound CC(C)C1=CC=CC(C(O)=O)=C1O XGAYQDWZIPRBPF-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 1
- ZWQBZEFLFSFEOS-UHFFFAOYSA-N 3,5-ditert-butyl-2-hydroxybenzoic acid Chemical compound CC(C)(C)C1=CC(C(O)=O)=C(O)C(C(C)(C)C)=C1 ZWQBZEFLFSFEOS-UHFFFAOYSA-N 0.000 description 1
- JCGRUCSGOUFSCY-UHFFFAOYSA-N 3-chloro-2-hydroxy-5-(1-phenylethyl)benzoic acid Chemical compound C=1C(Cl)=C(O)C(C(O)=O)=CC=1C(C)C1=CC=CC=C1 JCGRUCSGOUFSCY-UHFFFAOYSA-N 0.000 description 1
- HINSTNAJIHVPOM-UHFFFAOYSA-N 3-cyclohexyl-4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C(C2CCCCC2)=C1 HINSTNAJIHVPOM-UHFFFAOYSA-N 0.000 description 1
- BOTKTAZUSYVSFF-UHFFFAOYSA-N 4-(2,4,4-trimethylpentan-2-yl)benzene-1,2-diol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(O)C(O)=C1 BOTKTAZUSYVSFF-UHFFFAOYSA-N 0.000 description 1
- QHPQWRBYOIRBIT-UHFFFAOYSA-N 4-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C=C1 QHPQWRBYOIRBIT-UHFFFAOYSA-N 0.000 description 1
- PXOYSVWEZHSGNE-UHFFFAOYSA-N 6-butylidenecyclohexa-2,4-dien-1-ol Chemical group C(CCC)=C1C(C=CC=C1)O PXOYSVWEZHSGNE-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Landscapes
- Heat Sensitive Colour Forming Recording (AREA)
- Color Printing (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、感圧複写紙や感熱記録紙に用いられているロ
イコ系色素に関し、特に発色性および耐退色性、耐光性
に優れ、白色度の高いロイコ系色素用顕色剤に関するも
のである。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to leuco dyes used in pressure-sensitive copying paper and heat-sensitive recording paper. This invention relates to a color developer for leuco dyes with a high degree of strength.
近年、情報産業の急速な発展にともない、産業用、オフ
ィス用などの情報機器の端末から、容易に記録出力が得
られる感圧複写紙や感熱記録紙の利用が盛んに行われて
いる。2. Description of the Related Art In recent years, with the rapid development of the information industry, pressure-sensitive copying paper and thermal recording paper, which can easily obtain recording output from information equipment terminals for industrial use, office use, etc., have been widely used.
本発明は、上記感圧複写紙や上記感熱記録紙に用いられ
ているロイコ系色素用顕色剤として、5iQzおよび周
期律表第yb族の酸化物の混合物を用いることによって
、発色性および耐退色性。The present invention improves color development and fastness by using a mixture of 5iQz and oxides of group Yb of the periodic table as a color developer for leuco dyes used in the pressure-sensitive copying paper and the heat-sensitive recording paper. Fading property.
耐光性に優れた記録を得ることができるようにしたロイ
コ系色素用顕色剤を提供することを目的としている。The object of the present invention is to provide a color developer for leuco dyes that enables recording with excellent light resistance.
従来のロイコ系色素用顕色剤としては、α−ナフトール
、β−ナフトール、2・2′−メチレンビス(4−メチ
ル−6−タージヤリーイソブチルフエノール)、2・2
′−メチレンビス(4−クロルフェノール)、4フエニ
ルフエノール、4−ターシャリプチルフェノール、2・
2′−ジヒドロキシジフェノール、4・4′−セカンダ
リ−ブチリデンフェノール、4・4′−ジクロルヘキシ
リジンジフェノール、4−ヒドロキシジフェノキシド、
4・4′−イソプロピリデンジフェノール、ハイドロキ
ノン、4−ヒドロキシアセトフェノール、4・4′−イ
ソビリデンビス(2−ターシャリ−ブチルフェノール)
、4−ターシャリ−オクチルカテコール、ノボラック型
フェノール樹脂、フェノール重合体などのフェノール性
化合物や、サリチル酸、3−(α−メチルヘン)サリチ
ル酸、3・5−ジ−α−α−メチルヘンシルサリチル酸
、3−イソプロピルサリチル酸、3−クロル−5−(α
−メチルベンジル)サリチル酸、3−フェニル−5−(
α・α−ジメチルヘンシル)サリチル酸、3−ヘンシル
サリチル酸、3・5−ジターシャリブチルサリチル酸、
3−クーシャリブチルサリチル酸、安息香酸、テレフタ
ル酸、3・5−ジメチル−4−ヒドロキシ安息香酸、パ
ラターシャリブチル安息香酸、3−セカンダリブチル−
4=ヒドロキシ安息香酸、トリクロル安息香酸、3−シ
クロへキシル−4−ヒドロキシ安息香酸などの芳香族カ
ルボン酸、及びこれらフェノール性化合物や、活性白土
、酸性白土、ケイ酸アルミニウム、ベントナイト、アク
パルガイド、コロイダルシリカなどの固体酸や、マグネ
シウム、アルミニウム、カルシウム、チタン、マンガン
、スズ、ニッケルなどの多価金属と芳香族カルボン酸と
の塩などの有機酸性物質が使用されている。Conventional color developers for leuco dyes include α-naphthol, β-naphthol, 2,2'-methylenebis(4-methyl-6-tertiary isobutylphenol), 2,2
'-Methylenebis(4-chlorophenol), 4-phenylphenol, 4-tertiarybutylphenol, 2.
2'-dihydroxydiphenol, 4,4'-secondary butylidenephenol, 4,4'-dichlorhexylidine diphenol, 4-hydroxydiphenoxide,
4,4'-isopropylidene diphenol, hydroquinone, 4-hydroxyacetophenol, 4,4'-isopylidene bis(2-tert-butylphenol)
, 4-tert-octylcatechol, novolak type phenolic resin, phenolic polymers and other phenolic compounds, salicylic acid, 3-(α-methylhen)salicylic acid, 3,5-di-α-α-methylhensylsalicylic acid, 3 -isopropylsalicylic acid, 3-chloro-5-(α
-methylbenzyl)salicylic acid, 3-phenyl-5-(
α・α-dimethylhensyl) salicylic acid, 3-hensylsalicylic acid, 3,5-ditertiarybutylsalicylic acid,
3-Cushabutylsalicylic acid, benzoic acid, terephthalic acid, 3,5-dimethyl-4-hydroxybenzoic acid, para-tertiarybutylbenzoic acid, 3-sec-butyl-
4 = Aromatic carboxylic acids such as hydroxybenzoic acid, trichlorobenzoic acid, 3-cyclohexyl-4-hydroxybenzoic acid, and these phenolic compounds, activated clay, acid clay, aluminum silicate, bentonite, acpal guide , solid acids such as colloidal silica, and organic acidic substances such as salts of aromatic carboxylic acids and polyvalent metals such as magnesium, aluminum, calcium, titanium, manganese, tin, and nickel are used.
しかし、従来の有機化合物をロイコ系色素用顕色剤とし
て用いた場合、発色性があまり良好でなく、退色すると
いう問題があった。また、光照射による着色や大気中の
窒素化合物の似よる黄変が激しいなど問題があった。ま
た、活性白土などは、黄色味を帯びており良好な画像を
得ることができなかった。However, when conventional organic compounds are used as color developers for leuco dyes, there is a problem in that the color development is not very good and the color fades. In addition, there were problems such as coloring due to light irradiation and severe yellowing caused by nitrogen compounds in the atmosphere. In addition, activated clay has a yellowish tinge, making it impossible to obtain good images.
そこで、本発明は従来のこの様な問題点を解決するため
に、発色性に優れ、また耐退色性、耐光性に優れ、白色
度の高いロイコ系色素用顕色剤を提供することを目的と
している。Therefore, in order to solve these conventional problems, it is an object of the present invention to provide a color developer for leuco dyes that has excellent color development, excellent fading resistance, light resistance, and high whiteness. It is said that
本発明は、上記課題を解決するために、ロイコ系色素用
顕色剤として、S i Ozを用いさらにこのSiO□
の酸性度を増すために、Tie、やZro、などの周期
律表第IVb族の酸化物を少なくとも1mIW以上Si
Oよに混合することによって、発色性を向上させ、また
、耐退色性、耐光性を向上させるようにしたものである
。さらに、Tie。In order to solve the above-mentioned problems, the present invention uses SiOz as a color developer for leuco dyes, and furthermore, this SiO□
Si
By mixing O, the color development property is improved, and the fading resistance and light resistance are also improved. Furthermore, Tie.
やZrO,などの周期律表第IVb族の酸化物は、白色
度も高いために、良好な画像を得られるようにしたもの
である。Oxides of group IVb of the periodic table, such as ZrO and ZrO, have a high degree of whiteness and are therefore used to obtain good images.
以下に本発明の実施例を示す。 Examples of the present invention are shown below.
実施例1
5%(W/W)の濃度のポリビニルアルコール水溶液5
0重量部に、5iOt20重量部、Ti0□10重量部
を伴に加え、ボールミルを用いて約24時間粉砕分散し
、顕色剤分散液とした。この顕色剤分散液をバーコータ
ーを用い、40g/n?の上質紙上に、20g/+yr
(乾燥重量)となるように塗工し、ロイコ系色素用顕色
シートとした。このロイコ系色素用顕色シートを、ロイ
コ系色素を用いた感圧複写紙と−合わせ、120 kg
/cmの圧力で発色させ、濃度を測定した。また、耐退
色性を調べるために、発色直後より500時間後に発色
濃度を測定した。Example 1 Polyvinyl alcohol aqueous solution 5 with a concentration of 5% (W/W)
0 parts by weight, 20 parts by weight of 5iOt and 10 parts by weight of Ti0□ were added together and pulverized and dispersed for about 24 hours using a ball mill to obtain a color developer dispersion. This color developer dispersion was coated with a bar coater at 40 g/n? 20g/+yr on high quality paper
(dry weight) to obtain a color developing sheet for leuco dyes. This color developer sheet for leuco dyes was combined with pressure-sensitive copying paper using leuco dyes, weighing 120 kg.
The color was developed under a pressure of /cm and the density was measured. Furthermore, in order to examine the resistance to fading, the color density was measured 500 hours after color development.
以上の測定値を表1に示す。The above measured values are shown in Table 1.
実施例2
5%(W/W)の濃度のポリビニルアルコール水溶液5
0重量部に、S i Ox 20重量部、Zr0゜10
重量部を伴に加え、ボールミルを用い約24時間粉砕分
散し、顕色剤分散液とした。これを実施例1を同様の方
法により、ロイコ系色素用顕色シートを作製し、実施例
1と同様な測定を行った。Example 2 Polyvinyl alcohol aqueous solution 5 with a concentration of 5% (W/W)
0 parts by weight, 20 parts by weight of S i Ox, Zr0°10
Parts by weight were added together and pulverized and dispersed for about 24 hours using a ball mill to obtain a color developer dispersion. A color developing sheet for leuco dye was prepared using the same method as in Example 1, and the same measurements as in Example 1 were performed.
以上の測定値を表1に示す。The above measured values are shown in Table 1.
実施例3
5%(W/W)の濃度のポリビニルアルコール水溶液5
0重量部に、5iOz20重量部、Tie25重量部、
Z r O@ 5重量部を伴に加え、ボールミルを用い
て約24時間粉砕分散し、顕色剤分散液とした。これを
実施例1.2と同様の方法により、ロイコ系色素用顕色
シートを作製し、実施例1゜2と同様な測定を行った0
以上の測定値を表1に示す。Example 3 Polyvinyl alcohol aqueous solution 5 with a concentration of 5% (W/W)
0 parts by weight, 20 parts by weight of 5iOz, 25 parts by weight of Tie,
5 parts by weight of ZrO@ were added thereto, and the mixture was pulverized and dispersed for about 24 hours using a ball mill to obtain a color developer dispersion. A color developing sheet for leuco dye was prepared using the same method as in Example 1.2, and the same measurements as in Example 1.2 were carried out.
The above measured values are shown in Table 1.
比較例
上記の実施例と比較するために、公知のロイコ系色素用
顕色剤のひとつである、ビスフェノールAについて、実
施例1.2.3と同様の測定を行い、測定値を表1に示
す。Comparative Example In order to compare with the above example, bisphenol A, which is one of the known color developers for leuco dyes, was measured in the same manner as in Example 1.2.3, and the measured values are shown in Table 1. show.
表 1
[発明の効果〕
以上のように、ロイコ系色素用顕色剤として、stow
および周期律表第rVb族の酸化物を少なくとも1種類
以上含有した混合物を用いることによって、発色性に優
れ、また耐退色性、耐光性に優れ、白色塵の高いロイコ
系色素用顕色剤を提供することができる。Table 1 [Effects of the invention] As described above, stow is used as a color developer for leuco dyes.
By using a mixture containing at least one type of oxide of group rVb of the periodic table, we can create a color developer for leuco dyes that has excellent color development, fade resistance, light resistance, and high white dust. can be provided.
以上 出願人 セイコー電子工業株式会社that's all Applicant: Seiko Electronics Industries Co., Ltd.
Claims (1)
第IVb族の酸化物を少なくとも1種類以上含有する混合
物を用いたことを特徴とするロイコ系色素用顕色剤。A color developer for leuco dyes, characterized in that a mixture containing SiO_2 and at least one oxide of group IVb of the periodic table is used as a color developer for leuco dyes.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63112951A JPH01283184A (en) | 1988-05-10 | 1988-05-10 | Color developer for leuco dye |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63112951A JPH01283184A (en) | 1988-05-10 | 1988-05-10 | Color developer for leuco dye |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01283184A true JPH01283184A (en) | 1989-11-14 |
Family
ID=14599608
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63112951A Pending JPH01283184A (en) | 1988-05-10 | 1988-05-10 | Color developer for leuco dye |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01283184A (en) |
-
1988
- 1988-05-10 JP JP63112951A patent/JPH01283184A/en active Pending
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