JPH0267379A - Screen printing ink - Google Patents
Screen printing inkInfo
- Publication number
- JPH0267379A JPH0267379A JP63219051A JP21905188A JPH0267379A JP H0267379 A JPH0267379 A JP H0267379A JP 63219051 A JP63219051 A JP 63219051A JP 21905188 A JP21905188 A JP 21905188A JP H0267379 A JPH0267379 A JP H0267379A
- Authority
- JP
- Japan
- Prior art keywords
- carboxylic acid
- vehicle
- screen printing
- acid
- printing ink
- 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.)
- Granted
Links
- 238000007650 screen-printing Methods 0.000 title claims abstract description 9
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims abstract description 12
- -1 amine salt Chemical class 0.000 claims abstract description 8
- 150000002148 esters Chemical class 0.000 claims abstract description 8
- 239000000203 mixture Substances 0.000 claims description 25
- 150000001412 amines Chemical class 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 15
- 150000003863 ammonium salts Chemical group 0.000 claims description 11
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 abstract description 5
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 abstract description 4
- 150000003505 terpenes Chemical class 0.000 abstract description 4
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 abstract description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 2
- 239000000470 constituent Substances 0.000 abstract 2
- CJIAXHWXANNZPB-UHFFFAOYSA-N azanium;decanoate Chemical compound [NH4+].CCCCCCCCCC([O-])=O CJIAXHWXANNZPB-UHFFFAOYSA-N 0.000 abstract 1
- 238000013329 compounding Methods 0.000 abstract 1
- 239000000976 ink Substances 0.000 description 30
- 239000010408 film Substances 0.000 description 11
- 238000007639 printing Methods 0.000 description 10
- 239000002904 solvent Substances 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 150000001735 carboxylic acids Chemical group 0.000 description 4
- 239000000025 natural resin Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 2
- 235000007173 Abies balsamea Nutrition 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- 239000004857 Balsam Substances 0.000 description 2
- 229920002871 Dammar gum Polymers 0.000 description 2
- 241000147041 Guaiacum officinale Species 0.000 description 2
- 244000018716 Impatiens biflora Species 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 230000005587 bubbling Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 229940091561 guaiac Drugs 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 2
- MHVJRKBZMUDEEV-APQLOABGSA-N (+)-Pimaric acid Chemical compound [C@H]1([C@](CCC2)(C)C(O)=O)[C@@]2(C)[C@H]2CC[C@](C=C)(C)C=C2CC1 MHVJRKBZMUDEEV-APQLOABGSA-N 0.000 description 1
- MHVJRKBZMUDEEV-UHFFFAOYSA-N (-)-ent-pimara-8(14),15-dien-19-oic acid Natural products C1CCC(C(O)=O)(C)C2C1(C)C1CCC(C=C)(C)C=C1CC2 MHVJRKBZMUDEEV-UHFFFAOYSA-N 0.000 description 1
- WUOACPNHFRMFPN-SECBINFHSA-N (S)-(-)-alpha-terpineol Chemical compound CC1=CC[C@@H](C(C)(C)O)CC1 WUOACPNHFRMFPN-SECBINFHSA-N 0.000 description 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 1
- ARHIRDSNQLUBHR-UHFFFAOYSA-K 2-ethylhexanoate;indium(3+) Chemical compound [In+3].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O ARHIRDSNQLUBHR-UHFFFAOYSA-K 0.000 description 1
- GTOFXGPXYNYBEC-UHFFFAOYSA-K 2-ethylhexanoate;ruthenium(3+) Chemical compound [Ru+3].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O GTOFXGPXYNYBEC-UHFFFAOYSA-K 0.000 description 1
- QGJZLNKBHJESQX-UHFFFAOYSA-N 3-Epi-Betulin-Saeure Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C)CCC5(C(O)=O)CCC(C(=C)C)C5C4CCC3C21C QGJZLNKBHJESQX-UHFFFAOYSA-N 0.000 description 1
- CLOUCVRNYSHRCF-UHFFFAOYSA-N 3beta-Hydroxy-20(29)-Lupen-3,27-oic acid Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C(O)=O)CCC5(C)CCC(C(=C)C)C5C4CCC3C21C CLOUCVRNYSHRCF-UHFFFAOYSA-N 0.000 description 1
- MIJYXULNPSFWEK-GTOFXWBISA-N 3beta-hydroxyolean-12-en-28-oic acid Chemical compound C1C[C@H](O)C(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(C(O)=O)CCC(C)(C)C[C@H]5C4=CC[C@@H]3[C@]21C MIJYXULNPSFWEK-GTOFXWBISA-N 0.000 description 1
- OPAORDVBZRVVNQ-RNQWEJQRSA-N 4-[(z,2r)-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbut-3-enyl]-2-methoxyphenol Chemical compound C1=C(O)C(OC)=CC(C[C@@H](C)C(\C)=C/C=2C=C(OC)C(O)=CC=2)=C1 OPAORDVBZRVVNQ-RNQWEJQRSA-N 0.000 description 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
- 240000000972 Agathis dammara Species 0.000 description 1
- DIZWSDNSTNAYHK-XGWVBXMLSA-N Betulinic acid Natural products CC(=C)[C@@H]1C[C@H]([C@H]2CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5CC[C@@]34C)[C@@H]12)C(=O)O DIZWSDNSTNAYHK-XGWVBXMLSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000004859 Copal Substances 0.000 description 1
- 239000004860 Dammar gum Substances 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- JKLISIRFYWXLQG-UHFFFAOYSA-N Epioleonolsaeure Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C)CCC5(C(O)=O)CCC(C)(C)CC5C4CCC3C21C JKLISIRFYWXLQG-UHFFFAOYSA-N 0.000 description 1
- 241000782205 Guibourtia conjugata Species 0.000 description 1
- RWWVEQKPFPXLGL-ONCXSQPRSA-N L-Pimaric acid Chemical compound [C@H]1([C@](CCC2)(C)C(O)=O)[C@@]2(C)[C@H]2CC=C(C(C)C)C=C2CC1 RWWVEQKPFPXLGL-ONCXSQPRSA-N 0.000 description 1
- RWWVEQKPFPXLGL-UHFFFAOYSA-N Levopimaric acid Natural products C1CCC(C(O)=O)(C)C2C1(C)C1CC=C(C(C)C)C=C1CC2 RWWVEQKPFPXLGL-UHFFFAOYSA-N 0.000 description 1
- KGMSWPSAVZAMKR-UHFFFAOYSA-N Me ester-3, 22-Dihydroxy-29-hopanoic acid Natural products C1CCC(C(O)=O)(C)C2C1(C)C1CCC(=C(C)C)C=C1CC2 KGMSWPSAVZAMKR-UHFFFAOYSA-N 0.000 description 1
- KGMSWPSAVZAMKR-ONCXSQPRSA-N Neoabietic acid Chemical compound [C@H]1([C@](CCC2)(C)C(O)=O)[C@@]2(C)[C@H]2CCC(=C(C)C)C=C2CC1 KGMSWPSAVZAMKR-ONCXSQPRSA-N 0.000 description 1
- YBRJHZPWOMJYKQ-UHFFFAOYSA-N Oleanolic acid Natural products CC1(C)CC2C3=CCC4C5(C)CCC(O)C(C)(C)C5CCC4(C)C3(C)CCC2(C1)C(=O)O YBRJHZPWOMJYKQ-UHFFFAOYSA-N 0.000 description 1
- MIJYXULNPSFWEK-UHFFFAOYSA-N Oleanolinsaeure Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C)CCC5(C(O)=O)CCC(C)(C)CC5C4=CCC3C21C MIJYXULNPSFWEK-UHFFFAOYSA-N 0.000 description 1
- XURCIPRUUASYLR-UHFFFAOYSA-N Omeprazole sulfide Chemical compound N=1C2=CC(OC)=CC=C2NC=1SCC1=NC=C(C)C(OC)=C1C XURCIPRUUASYLR-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- OVKDFILSBMEKLT-UHFFFAOYSA-N alpha-Terpineol Natural products CC(=C)C1(O)CCC(C)=CC1 OVKDFILSBMEKLT-UHFFFAOYSA-N 0.000 description 1
- 229940088601 alpha-terpineol Drugs 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- JXSVIVRDWWRQRT-UYDOISQJSA-N asiatic acid Chemical compound C1[C@@H](O)[C@H](O)[C@@](C)(CO)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(C(O)=O)CC[C@@H](C)[C@H](C)[C@H]5C4=CC[C@@H]3[C@]21C JXSVIVRDWWRQRT-UYDOISQJSA-N 0.000 description 1
- VJFFDDQGMMQGTQ-UHFFFAOYSA-L barium(2+);2-ethylhexanoate Chemical compound [Ba+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O VJFFDDQGMMQGTQ-UHFFFAOYSA-L 0.000 description 1
- QGJZLNKBHJESQX-FZFNOLFKSA-N betulinic acid Chemical compound C1C[C@H](O)C(C)(C)[C@@H]2CC[C@@]3(C)[C@]4(C)CC[C@@]5(C(O)=O)CC[C@@H](C(=C)C)[C@@H]5[C@H]4CC[C@@H]3[C@]21C QGJZLNKBHJESQX-FZFNOLFKSA-N 0.000 description 1
- RXROCZREIWVERD-UHFFFAOYSA-L cadmium(2+);2-ethylhexanoate Chemical compound [Cd+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O RXROCZREIWVERD-UHFFFAOYSA-L 0.000 description 1
- SHZIWNPUGXLXDT-UHFFFAOYSA-N caproic acid ethyl ester Natural products CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- FCEOGYWNOSBEPV-FDGPNNRMSA-N cobalt;(z)-4-hydroxypent-3-en-2-one Chemical compound [Co].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O FCEOGYWNOSBEPV-FDGPNNRMSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- PZXJOHSZQAEJFE-UHFFFAOYSA-N dihydrobetulinic acid Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C)CCC5(C(O)=O)CCC(C(C)C)C5C4CCC3C21C PZXJOHSZQAEJFE-UHFFFAOYSA-N 0.000 description 1
- NKZSPGSOXYXWQA-UHFFFAOYSA-N dioxido(oxo)titanium;lead(2+) Chemical compound [Pb+2].[O-][Ti]([O-])=O NKZSPGSOXYXWQA-UHFFFAOYSA-N 0.000 description 1
- 150000004141 diterpene derivatives Chemical class 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 229930003658 monoterpene Natural products 0.000 description 1
- MQYXUWHLBZFQQO-UHFFFAOYSA-N nepehinol Natural products C1CC(O)C(C)(C)C2CCC3(C)C4(C)CCC5(C)CCC(C(=C)C)C5C4CCC3C21C MQYXUWHLBZFQQO-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229940100243 oleanolic acid Drugs 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- HZLWUYJLOIAQFC-UHFFFAOYSA-N prosapogenin PS-A Natural products C12CC(C)(C)CCC2(C(O)=O)CCC(C2(CCC3C4(C)C)C)(C)C1=CCC2C3(C)CCC4OC1OCC(O)C(O)C1O HZLWUYJLOIAQFC-UHFFFAOYSA-N 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、ビヒクル組成物を含有してなるスクリーン印
刷インキに関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to screen printing inks containing a vehicle composition.
従来の技術
テルペノイドに属するカルボン酸やそのエステルの組成
物は、ロジン(松脂)やグアヤク脂、カナダバルサム、
ダンマルなどと呼ばれ、植物が産する天然樹脂として知
られている。これらは従来よりワニスの形で塗料として
使われており、その性能も一定の評価を得て、工業的な
規模で広く利用されている。また、ビヒクルとして含有
され、スクリーン印刷インキ用としても、印刷性の良さ
や、顔料、溶剤との相溶性の良さなどから、主に高温焼
き付は形のインキに使用されている。Conventional technology Compositions of carboxylic acids and their esters belonging to terpenoids include rosin, guaiac, Canadian balsam,
It is known as dammaru, a natural resin produced by plants. These have traditionally been used as paints in the form of varnishes, and their performance has received a certain level of praise, and they are widely used on an industrial scale. It is also contained as a vehicle and is mainly used in high-temperature baking inks for screen printing inks due to its good printability and good compatibility with pigments and solvents.
発明が解決しようとする課題
商業的に流通し、利用できるテルペノイドに属するカル
ボン酸やそのエステル、もしくはその組成物は、印刷時
インキがスクリーン版のメツシュを通過する際に生ずる
泡が原因となって、ムラのない、平滑な印刷膜面を得る
ことが非常に困難であるという課題があった。Problems to be Solved by the Invention Carboxylic acids and their esters belonging to terpenoids, which are commercially available and can be used, or their compositions have problems that are caused by bubbles generated when ink passes through the mesh of a screen plate during printing. However, there was a problem in that it was very difficult to obtain a smooth and even printed film surface.
課題を解決するための手段
本発明では、ビヒクルをテルペノイドのカルボン酸やそ
のエステル、あるいはそれらの組成物に、一般式CnH
2n+1Cool (n=’+ 、2,3.・−−−−
−)で示される脂肪族カルボン酸のアンモニウム塩かア
ミンとの塩を混合させて構成することにより、前記の課
題を解決したものである。Means for Solving the Problems In the present invention, a vehicle of the general formula CnH is added to a terpenoid carboxylic acid, its ester, or a composition thereof.
2n+1Cool (n='+, 2, 3.・----
The above-mentioned problem is solved by mixing the ammonium salt of the aliphatic carboxylic acid represented by -) or the salt with an amine.
作用
一船人CnH,,n+1COOH(n= 1.2.3
、 ・−・・)で示される脂肪族カルボン酸のアンモニ
ウム塩かアミンとの塩は、無機塩と有機物との中間的な
性質を示し、テルペノイドのカルボン酸組成物や溶剤に
混合させた際、大部分は溶解するが、ごく一部が非常に
細かい粒子状となって析出し、顔料を含有させたかのよ
うな効果を組成物に与える。これによってインキにはチ
クソ性が付与され、印刷時のメソシュ通過によっても泡
が発生することなく被印刷物上に移されるようになる。Effect 1 shipman CnH,, n+1 COOH (n= 1.2.3
Ammonium salts of aliphatic carboxylic acids or salts with amines represented by , . Most of it dissolves, but a small portion precipitates in the form of very fine particles, giving the composition the effect of containing a pigment. This imparts thixotropic properties to the ink, allowing it to be transferred onto the printing substrate without generating bubbles even when the ink passes through the mesh during printing.
従って、非常に平滑でムラのない印刷膜面が得られるよ
うにするものである。Therefore, it is possible to obtain a very smooth and even printed film surface.
実施例 まず、本発明の概要について説明する。Example First, an overview of the present invention will be explained.
本発明で用いることのできるテルペノイドのカルボン酸
は、天然樹脂に含有される、例えばアビエチン酸とその
誘導体であるピマル酸、ネオアビエチン酸、レボピマル
酸など、また、グアヤコン酸とその誘導体、グアヤク酸
、ルペニン酸などである。さらには、ダンマルゴムに含
有されるダンマロール酸とその誘導体、ウルノル酸、オ
レアノール酸、ベツリン酸なども用いることができる。Terpenoid carboxylic acids that can be used in the present invention include those contained in natural resins, such as abietic acid and its derivatives, such as pimaric acid, neoabietic acid, and levopimaric acid, as well as guaiaconic acid and its derivatives, guaiacic acid, These include lupenic acid. Furthermore, dammarolic acid and its derivatives, urnolic acid, oleanolic acid, betulinic acid, etc. contained in dammar gum can also be used.
モノテルペノイドのカルボン酸は、常温で液体のものが
多いため、単独では使用できないが、前述のようなジテ
ルペノイドやトリテルペノイドのカルボン酸と混合すれ
ば使用してもよい。これらは、精製分離されたものが一
般には入手しがたく高価でもあるので、それらを含む天
然樹脂であるロジンやグアヤク脂、カナダバルサム、ダ
ンマル、コーパルなどを利用することができる。これら
のような天然樹脂は、産地やメーカーによって成分が大
幅に異なり、カルボン酸以外の成分も含まれていること
があるが、本発明の目的にはいっこうに差支えなく使用
できる。これ等のエステルとしては、主にアビエチン酸
のエステル類が使用でき、一般に市販されているロジン
エステルであれば、その種類は何でもよい。Most monoterpenoid carboxylic acids are liquid at room temperature, so they cannot be used alone, but they may be used if mixed with the aforementioned diterpenoid or triterpenoid carboxylic acids. These are generally difficult to obtain purified and separated and are expensive, so natural resins containing them such as rosin, guaiac, Canadian balsam, dammar, copal, etc. can be used. Natural resins such as these can be used without any problem for the purpose of the present invention, although their components vary widely depending on the region of production and manufacturer, and they may contain components other than carboxylic acids. As these esters, abietic acid esters can mainly be used, and any type of rosin ester that is generally commercially available may be used.
一船人CnH2n十、 C0OH(n =1.2,3.
・・−・・・)で示される脂肪族カルボン酸のアンモ
ニウム塩かアミンとの塩は、これらの酸とアンモニアや
アミン類との中和反応によって合成されたものが使用で
き、前記の式のnの値にも特に制限はない。しかしなが
ら、あまりアルキル基の短い例えば酢酸などの場合、こ
れと反応させるアミン類の炭素数を増加させたり、逆に
アルキル基の長い酸を用いる場合はこれと反応させるア
ミン類の炭素数を減少させたりする必要がある。これは
塩に無機塩的な性質と有機物的な性質を付与するという
ことを意味する。従って、アミン類については、第一級
、第二級、第三級のすべての種類及び脂肪族、芳香族。One shipman CnH2n10, C0OH (n = 1.2, 3.
The ammonium salts of aliphatic carboxylic acids or the salts with amines represented by the above formula can be synthesized by neutralizing these acids with ammonia or amines. There is also no particular limit to the value of n. However, if an acid with a short alkyl group, such as acetic acid, is used, the number of carbon atoms in the amine to be reacted with it must be increased, or conversely, if an acid with a long alkyl group is used, the number of carbon atoms in the amine to be reacted with it must be decreased. It is necessary to This means that it gives salt both inorganic salt properties and organic properties. Therefore, for amines, all types of primary, secondary, and tertiary, as well as aliphatic and aromatic.
複素環化合物の種類を問わず使えるが、そのアルキル基
に含まれる炭素数は、このようなことを考慮して使うの
が望ましい。Although any type of heterocyclic compound can be used, it is desirable to take this into consideration when determining the number of carbon atoms contained in the alkyl group.
次に具体的な実施例について説明する。Next, specific examples will be described.
(実施例1)
第1表に示した組成でビヒクルを10C1調製し、これ
らに2−エチルへキサン酸インジウムと2−エチルヘキ
サン酸すずを重量比で96=4に混合したものを1oダ
添加し、溶剤としてテトラリンを30g加えて混練し、
各組成の透明電極形成用スクリーン印刷インキを製造し
た。これらのインキを乳剤厚み16μm、250メツシ
ユのスクリーン版を用いてガラス基板上に1010mm
X30の矩形状パターンに印刷を行った。この被印刷物
を150’Cで30分間乾燥し、印刷膜面の評価を行っ
た。評価は、膜面のムラの有無とパターンエツジのダレ
の二点と、印刷時の泡立ちの有無で行った。(Example 1) 10C1 of vehicles were prepared with the composition shown in Table 1, and 10C of a mixture of indium 2-ethylhexanoate and tin 2-ethylhexanoate in a weight ratio of 96=4 was added. Then, 30g of tetralin was added as a solvent and kneaded.
Screen printing inks for forming transparent electrodes of various compositions were manufactured. These inks were applied onto a glass substrate in a size of 1010 mm using a 250 mesh screen plate with an emulsion thickness of 16 μm.
Printing was performed on a rectangular pattern of x30. This printing material was dried at 150'C for 30 minutes, and the surface of the printed film was evaluated. The evaluation was based on two points: the presence or absence of unevenness on the film surface, the sagging of the pattern edges, and the presence or absence of bubbling during printing.
これら評価結果も、第1表中に示した。これから分るよ
うに、脂肪族カルボン酸のアンモニウム塩かアばン類と
の塩を含有させたインキについては、印刷時の泡立ちが
なくなって印刷膜面が良好となる。その効果が現れる組
成については、用いたテルペノイドのカルボン酸の種類
と組成によって異なるが、第1表の結果から、良好なイ
ンキを得るために必要なこれら塩類の添加すべき最小量
は、アンモニア、第一級アミン、第二級アミン、第三級
アばンの順に増加していき、アミンの炭素数増加と共に
増加する傾向にあることが分る〇(実施例2)
第2表に示した組成でビヒクル1ooyを調製し、これ
に2−エチルへキサン酸鉛とチタン酸テトラn−ブチル
をモル比で1:1に混合したものを13F添加し、溶剤
としてα−ターピネオールを3Of加えて混練し、各組
成のチタン酸鉛薄膜形成用インキを製造した。これらの
インキを実施例1と同様な方法で評価した結果も第2表
中に示した。これから、実施例1と同様に、脂肪族カル
ボン酸のアンモニウム塩かアミン類との塩を含有するビ
ヒクルのインキが良好な膜面を与えることが分る。また
、第2表から、良好な印刷インキを得るためにビヒクル
中に含有させるべきこれら塩類の最小量は、アミンの炭
素数が増加するに伴って増大するということが分る。These evaluation results are also shown in Table 1. As can be seen, when the ink contains an ammonium salt of aliphatic carboxylic acid or a salt with an avant, there is no bubbling during printing, resulting in a good printed film surface. The composition in which this effect appears varies depending on the type and composition of the terpenoid carboxylic acid used, but from the results in Table 1, the minimum amount of these salts necessary to obtain a good ink is ammonia, It can be seen that primary amines, secondary amines, and tertiary amines increase in this order, and tend to increase as the number of carbon atoms in the amine increases.〇 (Example 2) Table 2 shows that Prepare a vehicle with the following composition, add 13F of a mixture of lead 2-ethylhexanoate and tetra-n-butyl titanate in a molar ratio of 1:1, add 3Of of α-terpineol as a solvent, and knead. Then, inks for forming lead titanate thin films having various compositions were manufactured. The results of evaluating these inks in the same manner as in Example 1 are also shown in Table 2. From this, it can be seen that, as in Example 1, the ink with the vehicle containing the ammonium salt of aliphatic carboxylic acid or the salt with amines gives a good film surface. It can also be seen from Table 2 that the minimum amount of these salts that must be included in the vehicle to obtain a good printing ink increases as the number of carbon atoms in the amine increases.
(以下余白)
(実施例3)
第3表に示した組成でビヒクル10oyを調製し、これ
に2−エチルヘキサン酸カドdウムと2−エチルヘキサ
ン酸すずをモル比で1:1に混合したものを15g添加
し、溶剤としてブチルセロソルブを3Of加えて混練し
、各組成の透明電極形成用インキを製造した。これらの
インキを実施例1と同じ方法で評価した結果も第3表中
に示した。これから、脂肪族カルボン酸のアンモニウム
塩かアミン類との塩を含有させたビヒクルのインキが良
好な印刷膜面を与え、良好な印刷インキを得るためにビ
ヒクル中に含有させるべきこれら塩類の最小量は、脂肪
族カルボン酸の炭素数が増加するに伴って増大するとい
うことが分る。(Left below) (Example 3) 10 oy of vehicle was prepared with the composition shown in Table 3, and cadmium 2-ethylhexanoate and tin 2-ethylhexanoate were mixed in a molar ratio of 1:1. 15g of the same were added, and 3Of of butyl cellosolve was added as a solvent and kneaded to produce inks for forming transparent electrodes of various compositions. The results of evaluating these inks using the same method as in Example 1 are also shown in Table 3. From this it can be seen that an ink with a vehicle containing ammonium salts of aliphatic carboxylic acids or salts with amines gives a good printing surface, and the minimum amount of these salts that should be contained in the vehicle to obtain a good printing ink. is found to increase as the number of carbon atoms in the aliphatic carboxylic acid increases.
(以 下 余 白)
(実施例4)
第4表に示した組成でビヒクル1oOgを調製し、これ
に硝酸インジウムと塩化第1すすをモル比で93=7に
混合したものを1(l添加し、溶剤としてブチルセロソ
ルブを3.Of加えて混練し、各組成の透明電極形成用
インキを製造した。これらのインキを実施例1と同じ方
法で評価した結果も第4表中に示した。これからも、前
述の実施例と同様、脂肪族カルボン酸のアンモニウム塩
かアミン類との塩を含有させたビヒクルのインキが良好
な印刷膜面を与えるということが分る。(Left below) (Example 4) 100g of vehicle was prepared with the composition shown in Table 4, and 1(l) of a mixture of indium nitrate and soot chloride in a molar ratio of 93=7 was added. 3.Of butyl cellosolve was added as a solvent and kneaded to produce inks for forming transparent electrodes of various compositions.The results of evaluating these inks using the same method as in Example 1 are also shown in Table 4. Similarly to the above-mentioned examples, it was found that an ink with a vehicle containing an ammonium salt of an aliphatic carboxylic acid or a salt with an amine gave a good printed film surface.
(以 下 余 白)
(実施例5)
実施例1と同じ組成でビヒクル100ダを調製し、これ
に2−エチルへキサン酸ルテニウムと2−エチルヘキサ
ン酸バリウムをモル比で1:1に混合したものを81添
加し、溶剤としてアセトフヱノンを3CI加えて混練し
、各組成の抵抗体形成用インキを製造した。これらのイ
ンキを実施例1と同じ方法で評価した結果を第6表に示
した。(Left below) (Example 5) A vehicle of 100 dah was prepared with the same composition as in Example 1, and ruthenium 2-ethylhexanoate and barium 2-ethylhexanoate were mixed in a molar ratio of 1:1. 3 CI of acetophenone as a solvent was added and kneaded to produce inks for forming resistors of various compositions. These inks were evaluated using the same method as in Example 1, and the results are shown in Table 6.
これからも、前述の実施例と同様、脂肪族カルボン酸の
アンモニウム塩かアミン類との塩を含有させたビヒクル
のインキが良好な印刷膜面を与えることが分り、その効
果が示された。As in the above-mentioned examples, it was found that ink with a vehicle containing an ammonium salt of an aliphatic carboxylic acid or a salt with an amine gave a good printed film surface, demonstrating its effectiveness.
(以 下 余 白)
(実施例6)
実施例2と同じ組成でビヒクル1oofを調製し、これ
に鉄ロアセチルアセトネートとコバルト(II)アセチ
ルアセトネートをモル比で1:1に混合したものを12
g添加し、溶剤としてイソホロンを30ダ加えて混練し
、各組成の磁性薄膜形成用インキを製造した。これらの
インキを実施例1と同じ方法で評価したところ、第6表
中に示した結果が得られた。これからも、前述の実施例
と同様、脂肪族カルボン酸のアンモニウム塩かアミン類
との塩を含有させたビヒクルのインキが良好な印刷膜面
を与えることが分り、その効果が示された。(Left below) (Example 6) A vehicle 1oof was prepared with the same composition as in Example 2, and iron loacetylacetonate and cobalt (II) acetylacetonate were mixed in a molar ratio of 1:1. 12
Then, 30 Da of isophorone was added as a solvent and kneaded to produce inks for forming magnetic thin films of various compositions. When these inks were evaluated in the same manner as in Example 1, the results shown in Table 6 were obtained. As in the above-mentioned examples, it was found that ink with a vehicle containing an ammonium salt of an aliphatic carboxylic acid or a salt with an amine gave a good printed film surface, demonstrating its effectiveness.
(以 下 余 白)
以上の実施例から分るように、本発明のビヒクル組成物
を含有する顔料を含有しないスクリーン印刷インキは印
刷膜面の特性を大きく向上させるものであり、添加すべ
き脂肪族カルボン酸のアンモニウム塩やアミンとの塩の
量は、膜形成剤として含まれる金属化合物によっても変
化するが、この量を適当に調整すればどのような化合物
の組合せでも、良好なスクリーン印刷インキとなるもの
である。(Margin below) As can be seen from the above examples, the pigment-free screen printing ink containing the vehicle composition of the present invention greatly improves the properties of the printed film surface, and the amount of fat to be added is The amount of ammonium salt of group carboxylic acid or salt with amine varies depending on the metal compound contained as a film-forming agent, but if this amount is appropriately adjusted, a good screen printing ink can be obtained regardless of the combination of compounds. This is the result.
発明の効果
以上の実施例から分るように、本発明のビヒクル組成物
を含有するスクリーン印刷インキは、ムラのない平滑な
印刷膜面を得ることができ、産業上の効果は大きいもの
である。Effects of the Invention As can be seen from the above examples, the screen printing ink containing the vehicle composition of the present invention can provide an even and smooth printed film surface, and has great industrial effects. .
Claims (1)
、一般式C_nH_2_n_+_1COOH(n=1、
2、3、・・・・・・)で示される脂肪族カルボン酸の
アンモニウム塩かアミンとの塩を主な構成成分とするビ
ヒクル組成物を含有してなるスクリーン印刷インキ。terpenoid carboxylic acid or their ester and the general formula C_nH_2_n_+_1COOH (n=1,
A screen printing ink comprising a vehicle composition whose main component is an ammonium salt of an aliphatic carboxylic acid or a salt with an amine represented by 2, 3, ...).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21905188A JP2650351B2 (en) | 1988-09-01 | 1988-09-01 | Screen printing ink |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP21905188A JP2650351B2 (en) | 1988-09-01 | 1988-09-01 | Screen printing ink |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0267379A true JPH0267379A (en) | 1990-03-07 |
JP2650351B2 JP2650351B2 (en) | 1997-09-03 |
Family
ID=16729494
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP21905188A Expired - Fee Related JP2650351B2 (en) | 1988-09-01 | 1988-09-01 | Screen printing ink |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2650351B2 (en) |
-
1988
- 1988-09-01 JP JP21905188A patent/JP2650351B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP2650351B2 (en) | 1997-09-03 |
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