JPH0745642B2 - Solvent composition for printing ink - Google Patents
Solvent composition for printing inkInfo
- Publication number
- JPH0745642B2 JPH0745642B2 JP61160566A JP16056686A JPH0745642B2 JP H0745642 B2 JPH0745642 B2 JP H0745642B2 JP 61160566 A JP61160566 A JP 61160566A JP 16056686 A JP16056686 A JP 16056686A JP H0745642 B2 JPH0745642 B2 JP H0745642B2
- Authority
- JP
- Japan
- Prior art keywords
- solvent
- resin
- ink
- paraffins
- odor
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000002904 solvent Substances 0.000 title claims description 45
- 239000000203 mixture Substances 0.000 title claims description 19
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 18
- 238000009835 boiling Methods 0.000 claims description 14
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 9
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 9
- 125000005329 tetralinyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 claims description 8
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 6
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 6
- 239000008096 xylene Substances 0.000 claims description 6
- 235000010290 biphenyl Nutrition 0.000 claims description 4
- 239000004305 biphenyl Substances 0.000 claims description 3
- 239000000976 ink Substances 0.000 description 24
- 229920005989 resin Polymers 0.000 description 21
- 239000011347 resin Substances 0.000 description 21
- 230000000052 comparative effect Effects 0.000 description 9
- 230000033228 biological regulation Effects 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 238000005984 hydrogenation reaction Methods 0.000 description 7
- 239000000049 pigment Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- 231100000419 toxicity Toxicity 0.000 description 6
- 230000001988 toxicity Effects 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000002480 mineral oil Substances 0.000 description 5
- 235000010446 mineral oil Nutrition 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000002966 varnish Substances 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 239000003350 kerosene Substances 0.000 description 3
- 231100000252 nontoxic Toxicity 0.000 description 3
- 230000003000 nontoxic effect Effects 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical class [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 230000036541 health Effects 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- 239000002808 molecular sieve Substances 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 2
- 239000000271 synthetic detergent Substances 0.000 description 2
- -1 Aromatic Hydrocarbons Aromatic hydrocarbons Chemical class 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 206010008428 Chemical poisoning Diseases 0.000 description 1
- HECLRDQVFMWTQS-UHFFFAOYSA-N Dicyclopentadiene Chemical compound C1C2C3CC=CC3C1C=C2 HECLRDQVFMWTQS-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 238000005899 aromatization reaction Methods 0.000 description 1
- 150000004074 biphenyls Chemical class 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 235000010187 litholrubine BK Nutrition 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- MOWMLACGTDMJRV-UHFFFAOYSA-N nickel tungsten Chemical compound [Ni].[W] MOWMLACGTDMJRV-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Landscapes
- Inks, Pencil-Leads, Or Crayons (AREA)
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は印刷インキ用溶剤に関する。TECHNICAL FIELD The present invention relates to a solvent for printing ink.
特に平版印刷インキに最適な無毒性溶剤に関する。Particularly, it relates to a non-toxic solvent most suitable for lithographic printing ink.
[従来技術およびその問題点] 従来、印刷インキ用溶剤、特に平版輪転印刷インキ用溶
剤として沸点230〜300℃の範囲内の各種の溶剤が使用さ
れていた。代表的なものは鉱油系の炭化水素溶剤であ
る。鉱油系の溶剤には次のような問題がある。すなわ
ち、鉱油は通常は芳香族成分を20〜30%含むので毒性上
の問題があり、連産品であるため沸点範囲が広くなり重
質成分を含むため、印刷後の乾燥性に劣る等である。[Prior Art and its Problems] Conventionally, various solvents having a boiling point of 230 to 300 ° C. have been used as a solvent for printing ink, particularly a solvent for lithographic printing ink. A typical example is a mineral oil hydrocarbon solvent. Mineral oil-based solvents have the following problems. That is, since mineral oil usually contains 20 to 30% of aromatic components, there is a problem of toxicity, and since it is a co-product, it has a wide boiling point range and contains heavy components, so that it is inferior in dryness after printing. .
芳香族成分のうちベンゼン、トルエン、キシレンは人体
に悪影響を及ぼすことから、これらの含有量の少ない溶
剤が強く要望されている。特に労働省令の特定化学物質
等障害予防規則ではベンゼン含有量が1vol%を越えるも
のについて、また同令の有機溶剤中毒予防規則ではトル
エンとキシレンの合計量が5wt%を越えるものについて
人体への悪影響が重視され、使用が厳しく制限されてい
る。また、これらの化合物は米国労働省制定の「化学物
質の危険有毒性の周知基準」による規制の対象となって
おり、これらの化合物の存在をを表示すること等が義務
付けられている。Among the aromatic components, benzene, toluene, and xylene have a bad effect on the human body, and thus there is a strong demand for a solvent having a low content of these. In particular, if the benzene content exceeds 1 vol% according to the Ordinance for Prevention of Disturbance of Specific Chemical Substances by the Ordinance of the Ministry of Labor, and if the total amount of toluene and xylene exceeds 5 wt% under the Ordinance for Prevention of Organic Solvent Poisoning of the same Ordinance, it has an adverse effect on the human body. Is emphasized and its use is severely restricted. In addition, these compounds are subject to regulation by the "Standards for Dangerous Toxicity of Chemical Substances" established by the US Department of Labor, and it is obligatory to indicate the presence of these compounds.
このような問題を解決するために、毒性のないパラフィ
ン類を混合することが試みられているが、パラフィン類
は低温で固化しやすい(5〜7℃で固化)、ワニスの流
動性を調整するのが困難、樹脂の溶解力不足等の問題が
生じる。また、ナフテン類を併用することも試みられて
いるが、ナフテン分を多くすると芳香族炭化水素に比べ
樹脂溶解性が低下し、印刷物の光沢が劣化する等の問題
が生じる。In order to solve such a problem, it has been attempted to mix non-toxic paraffins, but the paraffins easily solidify at low temperature (solidify at 5 to 7 ° C.) and adjust the fluidity of the varnish. However, there are problems such as difficulty in removing the resin and insufficient dissolving power of the resin. Further, it has been attempted to use naphthenes in combination, but if the naphthene content is increased, the solubility of the resin will be lower than that of the aromatic hydrocarbon and the gloss of the printed matter will be deteriorated.
[発明の目的] 本発明は、毒性がなく、臭気、樹脂溶解性、印刷物の光
沢、高速印刷性、ワニスの貯蔵安定性のいずれの要求性
能をも同時に満足するような溶剤の提供を目的とする。[Object of the Invention] An object of the present invention is to provide a solvent that is non-toxic and satisfies all the required properties of odor, resin solubility, gloss of printed matter, high-speed printability, and storage stability of varnish. To do.
[問題を解決するための手段] 本発明の前記目的は、ナフテン類30〜80wt%、イソパラ
フィン類15〜40wt%、n−パラフィン類0〜20w%、テ
トラリン類2〜15wt%、芳香族炭化水素0〜10wt%から
成る沸点230〜300℃の範囲内の本発明による印刷インキ
用溶剤組成物によって達成される。[Means for Solving the Problem] The object of the present invention is to provide naphthenes 30 to 80 wt%, isoparaffins 15 to 40 wt%, n-paraffins 0 to 20 w%, tetralines 2 to 15 wt%, and aromatic hydrocarbons. Achieved by a solvent composition for printing inks according to the invention having a boiling point in the range of 230 to 300 ° C. consisting of 0 to 10 wt%.
以下、本発明をさらに詳細に述べる。Hereinafter, the present invention will be described in more detail.
[発明の構成] 〔成分〕 本発明の溶剤の成分とは次のものをいう。[Constitution of Invention] [Component] The components of the solvent of the present invention are as follows.
(a) ナフテン類 1〜3環を主成分とする。単環と2環をほぼ等量ずつ主
成分として含むものが好ましい。ナフテン類は樹脂およ
び顔料の溶解性の向上および印刷物の光沢の向上に寄与
する。ナフテン類の含量は30〜80wt%であり、30%未満
のときは溶解力が不足し、80%を越えると臭気が好まし
くない。(A) Naphthenes 1 to 3 rings are the main components. It is preferable that the main component contains approximately equal amounts of monocycle and bicycle. Naphthenes contribute to improving the solubility of resins and pigments and improving the gloss of printed materials. The content of naphthenes is 30 to 80% by weight. When it is less than 30%, the dissolving power is insufficient, and when it exceeds 80%, the odor is not preferable.
(b) イソパラフィン類 イソパラフィン類は、臭気および低温特性の向上に寄与
する。イソパラフィン類の含量は15〜40wt%であり、15
%未満では改善効果が得られず、40%を越えると樹脂の
溶解力が低下する。(B) Isoparaffins Isoparaffins contribute to the improvement of odor and low temperature characteristics. The content of isoparaffins is 15-40wt%,
If it is less than 40%, the improvement effect cannot be obtained, and if it exceeds 40%, the dissolving power of the resin decreases.
(c) n−パラフィン類 n−パラフィン類は臭気改善効果に寄与する。含量は0
〜20wt%であり、20%を越えると樹脂の溶解力が低下す
ると共に、低温時のワニス粘度が上昇するので、含量は
できるだけ少ない方が好ましい。(C) n-paraffins n-paraffins contribute to the odor improving effect. Content is 0
The content is preferably up to 20% by weight, and when it exceeds 20%, the dissolving power of the resin decreases and the viscosity of the varnish at low temperature increases, so the content is preferably as low as possible.
(d) テトラリン類 テトラリン類としては、アルキルテトラリンが主成分で
ある。テトラリン類は樹脂および顔料の溶解力向上に寄
与する。含量は、2〜15wt%であり、2%未満では溶解
力不足であり、15%を越えると芳香族炭化水素と同様の
欠点、すなわち臭気等が現われてくる。(D) Tetralins As tetralins, alkyltetralin is the main component. Tetralins contribute to improving the dissolving power of resins and pigments. The content is 2 to 15% by weight, and if it is less than 2%, the dissolving power is insufficient, and if it exceeds 15%, the same drawbacks as aromatic hydrocarbons, that is, odor and the like appear.
(e) 芳香族炭化水素 芳香族炭化水素は法規制の対象外であるアルキルベンゼ
ン、アルキルナフタレン等の芳香族炭化水素が主成分で
あり、法規制の対象であるベンゼン、トルエン、キシレ
ンを実質的に含まないものである。また、法規制の対象
とはなっていないが、安全性の点で問題が懸念されるナ
フタレン、ビフェニル類をもほとんど含まない。この成
分は溶解力に寄与するが、できるだけ少い方が毒性およ
び臭気の点から好ましく、含量は0〜10wt%、さらに好
ましくは0〜5wt%である。(E) Aromatic Hydrocarbons Aromatic hydrocarbons are mainly composed of aromatic hydrocarbons such as alkylbenzene and alkylnaphthalene, which are not subject to legal regulation, and substantially benzene, toluene, and xylene, which are subject to legal regulations. It is not included. In addition, it does not include naphthalene and biphenyls, which are not subject to legal regulations but may cause problems in terms of safety. Although this component contributes to the dissolving power, it is preferably as small as possible from the viewpoint of toxicity and odor, and the content is 0 to 10 wt%, more preferably 0 to 5 wt%.
本発明は、芳香族炭化水素の含量をできるだけ少なくし
て、毒性問題を解決すると同時に他の成分の相乗左様に
よって、すぐれた性能を発揮させようとするものである
から、各成分およびその含有量が重要な意義を有する。
特にテトラリン類を必須成分として含有することが、本
発明の効果を奏する上で不可欠である。The present invention is intended to exert excellent performance by reducing the content of aromatic hydrocarbons as much as possible to solve the toxicity problem and at the same time, by synergistically working with other components, each component and its content. Has important significance.
In particular, the inclusion of tetralins as an essential component is indispensable for achieving the effects of the present invention.
本発明の溶剤の沸点範囲は230〜300℃である。230℃未
満の成分を含むときは、上記法規制の対象となる芳香族
成分が混入すると共に、印刷時の乾燥時の蒸発速度が速
すぎて、インキの粘度が増し、紙切れ現象が起り適切な
印刷ができない。300℃を越えると、乾燥速度が遅くな
り、印刷速度を上げられない。さらに好ましい沸点範囲
は245〜280℃である。The boiling range of the solvent of the present invention is 230 to 300 ° C. If it contains less than 230 ° C, the aromatic components that are subject to the above regulations will be mixed in, and the evaporation rate at the time of drying during printing will be too fast, which will increase the viscosity of the ink and cause a paper breakage phenomenon. Cannot print. When it exceeds 300 ° C, the drying speed becomes slow and the printing speed cannot be increased. A more preferable boiling point range is 245 to 280 ° C.
本発明の溶剤は、各成分化合物を混合することによって
得ることができるが、各成分を単離または合成した上で
所定の割合に混合することは必らずしも経済的ではな
い。The solvent of the present invention can be obtained by mixing each component compound, but it is not always economical to necessarily mix or synthesize each component at a predetermined ratio.
本発明の溶剤の好ましい製法は次の通りである。The preferred method for producing the solvent of the present invention is as follows.
石油系留分、好ましくは沸点範囲150〜300℃程度の灯油
留分を水素添加処理に供し、芳香族成分の大部分を核水
素化して、ナフテン類およびテトラリン類に軟化せし
め、同時に不純物である硫黄、窒素等の化合物を水素添
加により脱硫、脱窒する。この生成物からn−パラフィ
ン類の全部または一部をモレキュラーシーブ等で除去し
た後、蒸留により所望の沸点範囲および組成の溶剤留分
を得る。A petroleum-based fraction, preferably a kerosene fraction having a boiling point range of about 150 to 300 ° C, is subjected to a hydrogenation treatment, and most of the aromatic components are nuclear hydrogenated to be softened into naphthenes and tetralins, and at the same time are impurities. Compounds such as sulfur and nitrogen are desulfurized and denitrified by hydrogenation. After removing all or part of n-paraffins from this product with a molecular sieve or the like, distillation is performed to obtain a solvent fraction having a desired boiling range and composition.
水素添加の程度を調整して、所望の割合のナフテン類と
テトラリン類を含有せしめる。水素添加は圧力30〜100k
g/cm2、温度100〜300℃で、周期律表第VIII族遷移金属
等の公知の水素添加触媒の存在下で行なうのが好まし
い。反応形式は、回分式、連続式いずれも使用できる。The degree of hydrogenation is adjusted to contain a desired ratio of naphthenes and tetralins. Hydrogen addition pressure is 30-100k
It is preferably carried out at g / cm 2 and a temperature of 100 to 300 ° C. in the presence of a known hydrogenation catalyst such as a Group VIII transition metal of the periodic table. The reaction system may be either a batch system or a continuous system.
このようにして得られた溶剤留分に、適宜の成分を添加
して組成を調整することができる。この方法は、合成洗
剤原料等として大量に生産されているn−パラフィン類
を製造する方法における副生物の利用として、極めて経
済的なものである。The composition can be adjusted by adding appropriate components to the solvent fraction thus obtained. This method is extremely economical as the use of by-products in the method for producing n-paraffins that are produced in large quantities as raw materials for synthetic detergents.
(a) インキの種類 本発明の溶剤は、各種印刷インキに適用できるが、平版
用、特に輪転用インキに使用するのが好ましい。(A) Kind of Ink The solvent of the present invention can be applied to various printing inks, but it is preferably used for lithographic ink, especially for rotary ink.
(b) インキ用樹脂 インキ用樹脂として公知の各種樹脂を使用することがで
きる。例えば、石油樹脂およびその変性体、ロジン変性
フェノール樹脂、ロジン変性アルキド樹脂、脂肪酸また
は油変性アルキド樹脂等が目的に応じて単独または2種
以上混合して用いることができる。(B) Ink resin Various known resins can be used as the ink resin. For example, petroleum resin and its modified product, rosin-modified phenol resin, rosin-modified alkyd resin, fatty acid or oil-modified alkyd resin and the like can be used alone or in combination of two or more depending on the purpose.
(c) 他のインキ用成分 亜麻仁油、桐油、大豆油、脱水ヒマシ油等およびそれら
の重合体、変性体のごとき乾性油、半乾性油等を使用す
ることができる。(C) Other components for inks Linseed oil, tung oil, soybean oil, dehydrated castor oil and the like and drying oils such as polymers and modified products thereof, semi-drying oils and the like can be used.
着色剤として、有機顔料、無機顔料、螢光顔料、カーボ
ンブラック、金属粉等の各種の顔料を使用することがで
きる。As the colorant, various pigments such as organic pigments, inorganic pigments, fluorescent pigments, carbon black, and metal powder can be used.
以上の他、従来からインキ用に用いられている各種の添
加剤、例えばワックス、グリース、増粘剤、安定剤、分
散剤、充填剤、その他公知の添加剤を使用することがで
きる。In addition to the above, various additives conventionally used for inks such as wax, grease, thickener, stabilizer, dispersant, filler, and other known additives can be used.
[本発明の作用、効果] 本発明の溶液は各成分の相乗作用によって、各成分単独
では得られない効果を奏するものである。[Action and Effect of the Present Invention] The solution of the present invention exerts an effect that cannot be obtained by each component alone due to the synergistic action of each component.
すなわち、ナフテン類は樹脂および顔料の溶解力を増
し、印刷面の光沢を向上させ、イソパラフィンはn−パ
ラフィン類の欠点である溶解力不足、低温での難流動性
を解決し、さらにテトラリン類により樹脂および顔料の
溶解力を相乗効果的に向上させ、他方で芳香族炭化水素
を極力抑えて、毒性、臭気、安全性を解決し、かつn−
パラフィン類を減少させて溶解力、低温流動性における
欠点を解決した。That is, naphthenes increase the dissolving power of resins and pigments and improve the gloss of the printed surface, and isoparaffin solves the disadvantages of n-paraffins such as lack of dissolving power and poor flowability at low temperature. Synergistically improve the dissolving power of resin and pigment, while suppressing aromatic hydrocarbons as much as possible to solve toxicity, odor and safety, and n-
Paraffins were reduced to solve the drawbacks in solvency and low temperature fluidity.
本発明の溶剤は従来のインキ用溶剤と比較して、次のよ
うな利点がある。The solvent of the present invention has the following advantages as compared with conventional ink solvents.
(a) 法規制の対象であるベンゼン、トルエン、キシ
レンなどの芳香族を実質的に含まないため、環境汚染問
題が生じない。臭気の問題もない。(A) Since it does not substantially contain aromatic substances such as benzene, toluene, and xylene, which are subject to legal regulations, environmental pollution problems do not occur. There is no problem of odor.
(b) 毒性上問題のある芳香族炭化水素によって溶解
力を維持していた従来品と比較して、低芳香族化もしく
は無芳香族化にもかかわらず高溶解力を達成できる。(B) As compared with the conventional product in which the solvent power was maintained by an aromatic hydrocarbon which has a problem in toxicity, a high solvent power can be achieved in spite of the reduction in aromaticity or non-aromatization.
(c) n−パラフィン類の添加により低臭気性や低毒
性化を図っている従来品と比較して、溶剤自体およびイ
ンキワニスの低温時における高粘度化、流動性の低下が
生じない。(C) Compared with conventional products which have low odor and low toxicity due to the addition of n-paraffins, the solvent itself and the ink varnish do not have high viscosity and low fluidity at low temperature.
(d) 印刷物の光沢が優れている。(D) The gloss of the printed matter is excellent.
(e) 乾燥速度が速いので、印刷速度を向上させるこ
とができる。(E) Since the drying speed is high, the printing speed can be improved.
(f) 石油留分の水素添加、n−パラフィン類分離、
蒸留による一連の工程によって最適組成の溶剤が得られ
るので、従来のごとき複数の成分を用意して、混合する
という煩雑な作業が不要となる。特に、合成洗剤等の原
料として大量に生産されているn−パラフィン類製造時
の副生物を利用するときは、極めて経済的なものであ
る。(F) Hydrogenation of petroleum fraction, separation of n-paraffins,
Since the solvent having the optimum composition can be obtained by a series of steps by distillation, the complicated work of preparing a plurality of components and mixing them as in the conventional case is unnecessary. In particular, it is extremely economical when using a by-product in the production of n-paraffins, which is produced in large quantities as a raw material for synthetic detergents and the like.
(g) 上記(a)の安全性と関連するが、米国労働安
全衛生局(OSHA,Occupation,Safety and Health Admini
stration)制定の「化学物質等の危険有害性の周知基
準」で規制され、かつ表示義務のあるビフェニルおよび
ナフタレンを、本発明の組成物はほとんど含まないの
で、同法律の対象外になる。(G) In relation to the safety of (a) above, the US Occupational Safety and Health Administration (OSHA, Occupation, Safety and Health Admini
stration) Biphenyl and naphthalene, which are regulated by the established "standards of hazards of chemical substances, etc." and which are obligatory to be labeled, are excluded from the law because the composition of the present invention hardly contains them.
[実 施 例] 以下、本発明を実施例、比較例によって詳述するが、本
発明の要旨を逸脱しない限り、これらの実施例のみに限
定されるものではない。[Examples] Hereinafter, the present invention will be described in detail with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples without departing from the gist of the present invention.
なお、この明細書を通して、温度は全て℃であり、部お
よび%は特記しない限り重量基準である。Throughout this specification, all temperatures are degrees Celsius and parts and percentages are by weight unless otherwise stated.
(a) 溶剤およびその製造 実施例 1 原油の蒸留によって得られた沸点範囲150℃〜280℃の灯
油留分(パラフィン類65wt%、ナフテン類25wt%、芳香
族10wt%)を280℃、90kg/cm2の条件下、触媒として、
ニッケル−タングステン触媒を用いて、水素添加し、得
られた生成物を分子篩を充填した分離塔に供給し、n−
パラフィン類を除去した。n−パラフィン類が減少した
留分についで蒸留して、沸点243〜275℃の溶剤留分を得
た。この溶剤の組成および性状を表−1に示す。(A) Solvent and its production Example 1 Kerosene fraction (65 wt% of paraffins, 25 wt% of naphthenes, 10 wt% of aromatics) having a boiling range of 150 ° C to 280 ° C obtained by distillation of crude oil was added at 280 ° C, 90 kg / As a catalyst under the condition of cm 2 ,
Hydrogenation was performed using a nickel-tungsten catalyst, and the obtained product was supplied to a separation column packed with a molecular sieve, and n-
Paraffins were removed. The fraction depleted in n-paraffins was then distilled to obtain a solvent fraction having a boiling point of 243-275 ° C. The composition and properties of this solvent are shown in Table 1.
実施例 2 実施例1と異なる性状の灯油留分を用いて、実施例1と
同様の操作によって表−1に示す組成、性状の溶剤を得
た。Example 2 Using a kerosene fraction having properties different from those of Example 1, a solvent having the composition and properties shown in Table 1 was obtained by the same operation as in Example 1.
比較例 1 実施例1における水素添加をテトラリン含有量が0wt%
になる条件で行なって得た。溶剤の組成と性状を表−1
に示す。Comparative Example 1 Tetralin content was 0 wt% for hydrogenation in Example 1.
It was obtained by performing under the following conditions. Table 1 shows the composition and properties of the solvent.
Shown in.
比較例 2 市販の鉱油系溶剤(沸点235〜290℃)と、n−パラフィ
ン(沸点244〜265℃)を等量混合した。この混合溶剤の
組成と性状を同じく表−1に示す。Comparative Example 2 A commercially available mineral oil solvent (boiling point 235 to 290 ° C) and n-paraffin (boiling point 244 to 265 ° C) were mixed in equal amounts. The composition and properties of this mixed solvent are also shown in Table 1.
比較例 3 市販の鉱油系溶剤(沸点235〜290℃)を用いた。組成と
性状を表−1に示す。Comparative Example 3 A commercially available mineral oil-based solvent (boiling point 235 to 290 ° C.) was used. The composition and properties are shown in Table 1.
(b) 溶剤の評価試験 表−2に記載の試験方法は次の通りである。(B) Solvent evaluation test The test method described in Table 2 is as follows.
(ア)臭気 あらかじめ臭気官能試験のトレーニングを受けた男女計
10名により、エアーコンディショニングされた室におい
て、各溶剤の臭気を次の判定基準に従い5段階表示で判
定させた。結果を不均点として示した。(A) Odor Total male and female trained in advance for odor sensory test
In the air-conditioned room, 10 people judged the odor of each solvent in 5 grades according to the following criteria. The result is shown as a disproportionate score.
1…ほとんど無臭 2…やや無臭 3…有臭 4…かなり強い臭気 5…強い臭気 (イ)樹脂の溶解性 はじめにDCPD系樹脂またはロジン変性フェノール樹脂
を、頭領の各溶剤に溶解させ、次に同一の溶剤を加える
ことにより樹脂濃度を徐々に低減させ、白濁した時点に
おける樹脂濃度をもって、樹脂の溶解性の基準とした。
より低い樹脂濃度を示す溶剤の方が樹脂に対する溶解性
が優れているといえる。1 ... Almost odorless 2 ... Slightly odorless 3 ... Odorous 4 ... Quite strong odor 5 ... Strong odor (a) Solubility of resin First, dissolve the DCPD resin or rosin-modified phenolic resin in each solvent of the head, and then the same. The resin concentration was gradually reduced by adding the above solvent, and the resin concentration at the time of turbidity was used as the standard for the solubility of the resin.
It can be said that the solvent having a lower resin concentration has better solubility in the resin.
(ウ)インキの貯蔵安定性 オフセット輪転用の代表的配合例である下記の処方でイ
ンキを製造した。処方 wt% ロジン変性フェノール樹脂 32.5 あまに油 13.0 顔料(カーミン6B) 17.5 溶剤 37.0 貯蔵安定性の評価方法はスプレッドメーターに上記処方
で配合したインキを入れ、25℃にて1分後のインキの広
がりの程度を測定した。インキの製造直後と1ヶ月間貯
蔵後の値の比(%)で示す。流動性が変化しない、すな
わち、低下しないものは100であり、低下するものは100
を越える数値を示す。(C) Storage stability of ink An ink was produced by the following formulation, which is a typical formulation example for offset rotary printing. Formulation wt% Rosin-modified phenolic resin 32.5 Flaxseed oil 13.0 Pigment (Carmine 6B) 17.5 Solvent 37.0 The storage stability was evaluated by putting the ink blended with the above formulation in a spread meter and spreading the ink after 1 minute at 25 ° C. Was measured. The ratio (%) of the value immediately after the production of the ink and the value after the storage for one month is shown. The liquidity does not change, that is, 100 does not decrease, 100 decreases.
Indicates a value that exceeds.
(エ)印刷物の光沢 上記(ウ)のインキ配合処方に従い製造したインキ0.4m
lをRIテスターによりアート紙上に展色し、24時間放置
後、60度−60度光沢計によりその光沢を測定した。(D) Gloss of printed matter Ink manufactured according to the ink formulation of (c) above 0.4 m
1 was spread on an art paper by an RI tester, left for 24 hours, and then its gloss was measured by a 60 ° -60 ° gloss meter.
(c) 評価結果 表−1に示したように、実施例1および2の溶剤はいず
れも法規制の対象となっているベンゼン、トルエン、キ
シレンおよびナフタレンやビフェニルを含まず、低温に
おける高粘度化が認められない。これに対して、比較例
2は−7℃で固化しており、比較例3は−10℃で粘度上
昇が著しい。(C) Evaluation results As shown in Table-1, the solvents of Examples 1 and 2 do not contain benzene, toluene, xylene, naphthalene or biphenyl, which are subject to legal regulation, and have high viscosity at low temperature. Is not recognized. On the other hand, Comparative Example 2 is solidified at -7 ° C, and Comparative Example 3 shows a remarkable increase in viscosity at -10 ° C.
表−2に示したように、表−1で良好な性状を示した比
較例1の溶剤は溶解性、貯蔵安定性、印刷物の光沢が劣
る。比較例2の溶剤は各項目とも良とやや良であるが、
前述のように−7℃で固化するから実用上支障がある。
比較例3の溶剤は前述の欠点の他に臭気が悪い。これに
対し、実施例1および2の溶剤は、表−2の各項目で優
れた性能を示している。As shown in Table-2, the solvent of Comparative Example 1 showing good properties in Table-1 is inferior in solubility, storage stability and gloss of the printed matter. Although the solvent of Comparative Example 2 is good and good for each item,
As described above, solidification occurs at -7 ° C, which is a practical problem.
The solvent of Comparative Example 3 has bad odor in addition to the above-mentioned drawbacks. On the other hand, the solvents of Examples 1 and 2 show excellent performance in each item of Table-2.
Claims (2)
15〜40wt%、n−パラフィン類0〜20wt%、テトラリン
類2〜15wt%および芳香族炭化水素0〜10wt%から成る
沸点230〜300℃の範囲内の印刷インキ用溶剤組成物。1. Naphthenes 30-80 wt%, isoparaffins
A solvent composition for a printing ink having a boiling point of 230 to 300 ° C., which comprises 15 to 40 wt%, 0 to 20 wt% of n-paraffins, 2 to 15 wt% of tetralins, and 0 to 10 wt% of aromatic hydrocarbons.
ン、トルエン、キシレン、ナフタレンおよびビフェニル
のいずれも含まないものである特許請求の範囲第1項記
載の印刷インキ用溶剤組成物。2. The solvent composition for a printing ink according to claim 1, wherein the aromatic hydrocarbon is substantially free of benzene, toluene, xylene, naphthalene and biphenyl.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61160566A JPH0745642B2 (en) | 1986-07-08 | 1986-07-08 | Solvent composition for printing ink |
| US07/069,510 US4795840A (en) | 1986-07-04 | 1987-07-02 | Method for preparing hydrocarbon mixture solvent |
| EP87109685A EP0255871B1 (en) | 1986-07-04 | 1987-07-03 | Use of a hydrocarbon mixture as solvent |
| DE8787109685T DE3782289T2 (en) | 1986-07-04 | 1987-07-03 | USE OF A HYDROCARBON MIXTURE AS A SOLVENT. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61160566A JPH0745642B2 (en) | 1986-07-08 | 1986-07-08 | Solvent composition for printing ink |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6315869A JPS6315869A (en) | 1988-01-22 |
| JPH0745642B2 true JPH0745642B2 (en) | 1995-05-17 |
Family
ID=15717747
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61160566A Expired - Fee Related JPH0745642B2 (en) | 1986-07-04 | 1986-07-08 | Solvent composition for printing ink |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0745642B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH086060B2 (en) * | 1987-06-13 | 1996-01-24 | 出光興産株式会社 | Ink solvent |
| JP3028679B2 (en) * | 1992-03-06 | 2000-04-04 | 東洋インキ製造株式会社 | Printing ink |
| JP2017110173A (en) * | 2015-12-15 | 2017-06-22 | 実 岡部 | Cleaning agents, deodorants and antibacterial agents and cleaning, deodorizing or antibacterial methods |
-
1986
- 1986-07-08 JP JP61160566A patent/JPH0745642B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6315869A (en) | 1988-01-22 |
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