CA2018954C - Methode de developpement de plaques d'impression photopolymerisables et compose connexe - Google Patents

Methode de developpement de plaques d'impression photopolymerisables et compose connexe

Info

Publication number: CA2018954C
Authority: CA; Canada
Prior art keywords: developer composition; methylpyrrolidone; nonionic surfactant; nonylphenolpolyethylene; limonene
Prior art date: 1990-05-10
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

Application number

CA 2018954

Other languages

English (en)

Other versions

CA2018954A1 (fr

Inventor

Victor L. Larimer

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

3D Agency Inc

Original Assignee

3D Agency Inc

Priority date (The priority date 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 date listed.)

1990-05-10

Filing date

1990-06-13

Publication date

1995-12-19

1990-06-13 Application filed by 3D Agency Inc filed Critical 3D Agency Inc

1991-11-10 Publication of CA2018954A1 publication Critical patent/CA2018954A1/fr

1995-12-19 Application granted granted Critical

1995-12-19 Publication of CA2018954C publication Critical patent/CA2018954C/fr

2010-06-13 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 76
238000000034 method Methods 0.000 title abstract description 10
238000007639 printing Methods 0.000 title description 8
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims abstract description 51
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims abstract description 22
239000002736 nonionic surfactant Substances 0.000 claims abstract description 17
229930003658 monoterpene Natural products 0.000 claims abstract description 14
150000002773 monoterpene derivatives Chemical class 0.000 claims abstract description 14
235000002577 monoterpenes Nutrition 0.000 claims abstract description 14
XMGQYMWWDOXHJM-JTQLQIEISA-N D-limonene Natural products CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 claims description 27
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 15
235000019445 benzyl alcohol Nutrition 0.000 claims description 13
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 claims description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 2
235000008331 Pinus X rigitaeda Nutrition 0.000 claims description 2
235000011613 Pinus brutia Nutrition 0.000 claims description 2
241000018646 Pinus brutia Species 0.000 claims description 2
150000003138 primary alcohols Chemical class 0.000 claims 2
125000000545 (4R)-limonene group Chemical group 0.000 claims 1
125000004432 carbon atom Chemical group C* 0.000 claims 1
BHXIWUJLHYHGSJ-UHFFFAOYSA-N ethyl 3-ethoxypropanoate Chemical compound CCOCCC(=O)OCC BHXIWUJLHYHGSJ-UHFFFAOYSA-N 0.000 claims 1
239000003960 organic solvent Substances 0.000 claims 1
230000005855 radiation Effects 0.000 abstract description 11
238000005406 washing Methods 0.000 abstract description 7
239000010410 layer Substances 0.000 description 24
239000000463 material Substances 0.000 description 17
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 8
238000011161 development Methods 0.000 description 7
-1 trichloroethylene, tetrachloroethylene Chemical group 0.000 description 7
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
238000009835 boiling Methods 0.000 description 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
229920001577 copolymer Polymers 0.000 description 3
238000001035 drying Methods 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
239000002904 solvent Substances 0.000 description 3
238000012360 testing method Methods 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
XMGQYMWWDOXHJM-SNVBAGLBSA-N (-)-α-limonene Chemical compound CC(=C)[C@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-SNVBAGLBSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
MOYAFQVGZZPNRA-UHFFFAOYSA-N Terpinolene Chemical compound CC(C)=C1CCC(C)=CC1 MOYAFQVGZZPNRA-UHFFFAOYSA-N 0.000 description 2
QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 2
UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
238000002156 mixing Methods 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
239000000178 monomer Substances 0.000 description 2
231100000252 nontoxic Toxicity 0.000 description 2
230000003000 nontoxic effect Effects 0.000 description 2
238000012545 processing Methods 0.000 description 2
238000000926 separation method Methods 0.000 description 2
230000008961 swelling Effects 0.000 description 2
239000002699 waste material Substances 0.000 description 2
DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
NFLGAXVYCFJBMK-RKDXNWHRSA-N (+)-isomenthone Natural products CC(C)[C@H]1CC[C@@H](C)CC1=O NFLGAXVYCFJBMK-RKDXNWHRSA-N 0.000 description 1
REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 1
QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 1
BALXAMAFSGBZFN-UHFFFAOYSA-N 1-nonyl-2-(2-nonylphenoxy)benzene Chemical class CCCCCCCCCC1=CC=CC=C1OC1=CC=CC=C1CCCCCCCCC BALXAMAFSGBZFN-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
NFLGAXVYCFJBMK-UHFFFAOYSA-N Menthone Chemical compound CC(C)C1CCC(C)CC1=O NFLGAXVYCFJBMK-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
229920000459 Nitrile rubber Polymers 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
238000012644 addition polymerization Methods 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 1
229940116229 borneol Drugs 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
235000000484 citronellol Nutrition 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
238000004880 explosion Methods 0.000 description 1
206010016256 fatigue Diseases 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
238000007689 inspection Methods 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
229930007503 menthone Natural products 0.000 description 1
229940043265 methyl isobutyl ketone Drugs 0.000 description 1
GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
238000005065 mining Methods 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
238000000643 oven drying Methods 0.000 description 1
229940086255 perform Drugs 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
229920002587 poly(1,3-butadiene) polymer Polymers 0.000 description 1
229920006122 polyamide resin Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
239000003505 polymerization initiator Substances 0.000 description 1
229920000136 polysorbate Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
239000011241 protective layer Substances 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000004065 semiconductor Substances 0.000 description 1
150000003384 small molecules Chemical class 0.000 description 1
239000012453 solvate Substances 0.000 description 1
230000002269 spontaneous effect Effects 0.000 description 1
238000001256 steam distillation Methods 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
150000003505 terpenes Chemical class 0.000 description 1
235000007586 terpenes Nutrition 0.000 description 1
229940116411 terpineol Drugs 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Landscapes

Photosensitive Polymer And Photoresist Processing (AREA)

CA 2018954 1990-05-10 1990-06-13 Methode de developpement de plaques d'impression photopolymerisables et compose connexe Expired - Fee Related CA2018954C (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US52189790A	1990-05-10	1990-05-10
US521,897		1990-05-10

Publications (2)

Publication Number	Publication Date
CA2018954A1 CA2018954A1 (fr)	1991-11-10
CA2018954C true CA2018954C (fr)	1995-12-19

Family

ID=24078596

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA 2018954 Expired - Fee Related CA2018954C (fr)	1990-05-10	1990-06-13	Methode de developpement de plaques d'impression photopolymerisables et compose connexe

Country Status (1)

Country	Link
CA (1)	CA2018954C (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US7588632B2 (en)	2002-01-24	2009-09-15	Biomatera Inc.	Biodegradable flexographic ink

1990
- 1990-06-13 CA CA 2018954 patent/CA2018954C/fr not_active Expired - Fee Related

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US7588632B2 (en)	2002-01-24	2009-09-15	Biomatera Inc.	Biodegradable flexographic ink

Also Published As

Publication number	Publication date
CA2018954A1 (fr)	1991-11-10

Legal Events

Date	Code	Title	Description
1993-05-11	EEER	Examination request
2004-06-14	MKLA	Lapsed

Publication	Publication Date	Title
US4806506A (en)	1989-02-21	Process for detackifying photopolymer flexographic printing plates
EP1046082B1 (fr)	2004-05-19	Procede de development de cliches d'impression photopolymeres
US8771925B2 (en)	2014-07-08	Flexographic processing solution and method of use
US5135837A (en)	1992-08-04	Photosensitive elastomeric element having improved solvent resistance
JPS5833884B2 (ja)	1983-07-22	光感受性弾性体状組成物
EP2529277B1 (fr)	2019-04-03	Solution de traitement flexographique et utilisation
JPH0769617B2 (ja)	1995-07-31	光重合により架橋されるレリ−フ版体の製造方法
EP0464398B1 (fr)	1998-04-01	Procédé pour la stabilisation dimensionnelle des plaques d'impression flexographiques photopolymères
US5204227A (en)	1993-04-20	Method of developing photopolymerizable printing plates and composition therefor
EP0504824B1 (fr)	1998-01-14	Elément d'impression photosensible
US5116720A (en)	1992-05-26	Developing solvent for layers which are crosslinkable by photopolymerization and process for the production of relief forms
US5312719A (en)	1994-05-17	Developing solvent for layers which are crosslinkable by photopolymerization and process for the production of relief forms
AU614674B2 (en)	1991-09-05	Developing solvent for layers which are crosslinkable by photopolymerization and process for the production of relief forms
CA2018954C (fr)	1995-12-19	Methode de developpement de plaques d'impression photopolymerisables et compose connexe
EP0439123A2 (fr)	1991-07-31	Procédé pour fabriquer une structure d'image photoréticulée
JPH02213844A (ja)	1990-08-24	耐オゾン性フレキソ印刷版の製法
EP0064564B1 (fr)	1985-08-28	Procédé pour le traitement des surfaces de plaques d'impression flexographiques contenant des copolymères de butadiène/acrylonitrile
WO1993015441A1 (fr)	1993-08-05	Procede de prepartion d'un element elastomere photodurcissable ayant une meilleure marge d'exposition
JPH0859885A (ja)	1996-03-05	表面粘着防止のためのポリマー組成物及び方法
JPH02213846A (ja)	1990-08-24	耐オゾン性フレキソ印刷版を製版するための光重合性エラストマー混合物およびこの混合物を含有する記録材料
JPH04285967A (ja)	1992-10-12	フレキソ印刷版用現像液
CA2067608A1 (fr)	1992-10-31	Melange solvant pour le developpement de couches d'enregistrement negatives

CA2018954C - Methode de developpement de plaques d'impression photopolymerisables et compose connexe - Google Patents

Info

Links

Landscapes

Applications Claiming Priority (2)

Publications (2)

Family

ID=24078596

Family Applications (1)

Country Status (1)

Cited By (1)

Cited By (1)

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