GB1193923A - Photopolymerizable Dispersions and Elements Containing Nonmigratory Photoreducible Dyes - Google Patents
Photopolymerizable Dispersions and Elements Containing Nonmigratory Photoreducible DyesInfo
- Publication number
- GB1193923A GB1193923A GB21848/68A GB2184868A GB1193923A GB 1193923 A GB1193923 A GB 1193923A GB 21848/68 A GB21848/68 A GB 21848/68A GB 2184868 A GB2184868 A GB 2184868A GB 1193923 A GB1193923 A GB 1193923A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dyes
- dye
- dispersions
- dispersion medium
- unsaturated compound
- 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
Links
- 239000000975 dye Substances 0.000 title abstract 9
- 239000006185 dispersion Substances 0.000 title abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 229920001577 copolymer Polymers 0.000 abstract 3
- 150000003254 radicals Chemical class 0.000 abstract 3
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 239000002612 dispersion medium Substances 0.000 abstract 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 abstract 2
- HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 abstract 2
- AMBFNDRKYCJLNH-UHFFFAOYSA-N 1-(3-piperidin-1-ylpropyl)piperidine Chemical compound C1CCCCN1CCCN1CCCCC1 AMBFNDRKYCJLNH-UHFFFAOYSA-N 0.000 abstract 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- GROXSGRIVDMIEN-UHFFFAOYSA-N 2-methyl-n-prop-2-enylprop-2-enamide Chemical compound CC(=C)C(=O)NCC=C GROXSGRIVDMIEN-UHFFFAOYSA-N 0.000 abstract 1
- KKAJSJJFBSOMGS-UHFFFAOYSA-N 3,6-diamino-10-methylacridinium chloride Chemical compound [Cl-].C1=C(N)C=C2[N+](C)=C(C=C(N)C=C3)C3=CC2=C1 KKAJSJJFBSOMGS-UHFFFAOYSA-N 0.000 abstract 1
- IICCLYANAQEHCI-UHFFFAOYSA-N 4,5,6,7-tetrachloro-3',6'-dihydroxy-2',4',5',7'-tetraiodospiro[2-benzofuran-3,9'-xanthene]-1-one Chemical compound O1C(=O)C(C(=C(Cl)C(Cl)=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 IICCLYANAQEHCI-UHFFFAOYSA-N 0.000 abstract 1
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 abstract 1
- 239000001828 Gelatine Substances 0.000 abstract 1
- 229920000084 Gum arabic Polymers 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- NPKSPKHJBVJUKB-UHFFFAOYSA-N N-phenylglycine Chemical compound OC(=O)CNC1=CC=CC=C1 NPKSPKHJBVJUKB-UHFFFAOYSA-N 0.000 abstract 1
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 abstract 1
- FCASKLHVRFDIJB-UHFFFAOYSA-N Riboflavine Natural products Cc1cc2N=C3C(NC(=O)NC3=O)N(CC(O)C(O)C(O)CO)c2cc1C FCASKLHVRFDIJB-UHFFFAOYSA-N 0.000 abstract 1
- 241000978776 Senegalia senegal Species 0.000 abstract 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 abstract 1
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 abstract 1
- 235000010489 acacia gum Nutrition 0.000 abstract 1
- 239000000205 acacia gum Substances 0.000 abstract 1
- 229940023020 acriflavine Drugs 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 239000008346 aqueous phase Substances 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 229960001506 brilliant green Drugs 0.000 abstract 1
- HXCILVUBKWANLN-UHFFFAOYSA-N brilliant green cation Chemical compound C1=CC(N(CC)CC)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](CC)CC)C=C1 HXCILVUBKWANLN-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- ZXJXZNDDNMQXFV-UHFFFAOYSA-M crystal violet Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1[C+](C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 ZXJXZNDDNMQXFV-UHFFFAOYSA-M 0.000 abstract 1
- BADXJIPKFRBFOT-UHFFFAOYSA-N dimedone Chemical compound CC1(C)CC(=O)CC(=O)C1 BADXJIPKFRBFOT-UHFFFAOYSA-N 0.000 abstract 1
- 239000004815 dispersion polymer Substances 0.000 abstract 1
- SEACYXSIPDVVMV-UHFFFAOYSA-L eosin Y Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 SEACYXSIPDVVMV-UHFFFAOYSA-L 0.000 abstract 1
- 125000003700 epoxy group Chemical group 0.000 abstract 1
- IINNWAYUJNWZRM-UHFFFAOYSA-L erythrosin B Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 IINNWAYUJNWZRM-UHFFFAOYSA-L 0.000 abstract 1
- 229940011411 erythrosine Drugs 0.000 abstract 1
- 239000004174 erythrosine Substances 0.000 abstract 1
- 235000012732 erythrosine Nutrition 0.000 abstract 1
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 abstract 1
- 229960002143 fluorescein Drugs 0.000 abstract 1
- 229920000159 gelatin Polymers 0.000 abstract 1
- 235000019322 gelatine Nutrition 0.000 abstract 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 abstract 1
- 239000004615 ingredient Substances 0.000 abstract 1
- 239000003999 initiator Substances 0.000 abstract 1
- 239000002609 medium Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229940012189 methyl orange Drugs 0.000 abstract 1
- STZCRXQWRGQSJD-GEEYTBSJSA-M methyl orange Chemical compound [Na+].C1=CC(N(C)C)=CC=C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 STZCRXQWRGQSJD-GEEYTBSJSA-M 0.000 abstract 1
- 230000001617 migratory effect Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- YQCFXPARMSSRRK-UHFFFAOYSA-N n-[6-(prop-2-enoylamino)hexyl]prop-2-enamide Chemical compound C=CC(=O)NCCCCCCNC(=O)C=C YQCFXPARMSSRRK-UHFFFAOYSA-N 0.000 abstract 1
- 239000012071 phase Substances 0.000 abstract 1
- 125000001484 phenothiazinyl group Chemical class C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 abstract 1
- GVKCHTBDSMQENH-UHFFFAOYSA-L phloxine B Chemical compound [Na+].[Na+].[O-]C(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 GVKCHTBDSMQENH-UHFFFAOYSA-L 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 abstract 1
- 229940043267 rhodamine b Drugs 0.000 abstract 1
- 229960002477 riboflavin Drugs 0.000 abstract 1
- 239000002151 riboflavin Substances 0.000 abstract 1
- 235000019192 riboflavin Nutrition 0.000 abstract 1
- 238000007142 ring opening reaction Methods 0.000 abstract 1
- 229940081623 rose bengal Drugs 0.000 abstract 1
- 229930187593 rose bengal Natural products 0.000 abstract 1
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 abstract 1
- OARRHUQTFTUEOS-UHFFFAOYSA-N safranin Chemical compound [Cl-].C=12C=C(N)C(C)=CC2=NC2=CC(C)=C(N)C=C2[N+]=1C1=CC=CC=C1 OARRHUQTFTUEOS-UHFFFAOYSA-N 0.000 abstract 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 abstract 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/09—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers
- G03F7/105—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers having substances, e.g. indicators, for forming visible images
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B17/00—Azine dyes
- C09B17/02—Azine dyes of the benzene series
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
- G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
- G03F7/031—Organic compounds not covered by group G03F7/029
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/1053—Imaging affecting physical property or radiation sensitive material, or producing nonplanar or printing surface - process, composition, or product: radiation sensitive composition or product or process of making binder containing
- Y10S430/1055—Radiation sensitive composition or product or process of making
- Y10S430/114—Initiator containing
- Y10S430/117—Free radical
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/1053—Imaging affecting physical property or radiation sensitive material, or producing nonplanar or printing surface - process, composition, or product: radiation sensitive composition or product or process of making binder containing
- Y10S430/1055—Radiation sensitive composition or product or process of making
- Y10S430/127—Spectral sensitizer containing
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Architecture (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Structural Engineering (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymerisation Methods In General (AREA)
- Optical Filters (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US64049667A | 1967-05-23 | 1967-05-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1193923A true GB1193923A (en) | 1970-06-03 |
Family
ID=24568496
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB21848/68A Expired GB1193923A (en) | 1967-05-23 | 1968-05-08 | Photopolymerizable Dispersions and Elements Containing Nonmigratory Photoreducible Dyes |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3579339A (en:Method) |
| BE (1) | BE715520A (en:Method) |
| DE (1) | DE1769359C3 (en:Method) |
| GB (1) | GB1193923A (en:Method) |
Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2438672A1 (fr) * | 1978-10-13 | 1980-05-09 | Ciba Geigy Ag | Colorants contenant des groupes amino ou imino |
| US4399209A (en) | 1981-11-12 | 1983-08-16 | The Mead Corporation | Transfer imaging system |
| US4416966A (en) | 1982-08-25 | 1983-11-22 | The Mead Corporation | Capsular imaging system comprising decolorizing agent |
| GB2133899A (en) * | 1983-01-17 | 1984-08-01 | Mead Corp | Improved imaging system |
| GB2135468A (en) * | 1983-02-15 | 1984-08-30 | Mead Corp | Photosensitive material employing encapsulated radiation sensitive composition and process for improving sensitivity by sequestering oxygen |
| US4508807A (en) * | 1983-07-11 | 1985-04-02 | Mead Corporation | Photosensitive material employing encapsulated radiation sensitive composition and a transparentizable image-receiving layer |
| US4562137A (en) * | 1982-12-30 | 1985-12-31 | The Mead Corporation | Photosensitive material employing encapsulated radiation sensitive composition |
| US4822714A (en) * | 1981-11-12 | 1989-04-18 | The Mead Corporation | Transfer imaging system |
| US4842976A (en) * | 1982-01-18 | 1989-06-27 | Mead Corp. | Color image-forming process |
| EP0284938A3 (en) * | 1987-03-28 | 1989-08-30 | Hoechst Aktiengesellschaft | Photopolymerisable composition and registration material prepared therewith |
| EP0287817A3 (en) * | 1987-03-28 | 1989-08-30 | Hoechst Aktiengesellschaft | Photopolymerisable composition and registration material prepared therewith |
| EP0321826A3 (en) * | 1987-12-22 | 1989-08-30 | Hoechst Aktiengesellschaft | Photopolymerisable mixture and recording material manufactured therefrom |
| EP0321827A3 (en) * | 1987-12-22 | 1989-09-06 | Hoechst Aktiengesellschaft | Photopolymerisable mixture and recording material manufactured therefrom |
| US4903991A (en) * | 1983-07-18 | 1990-02-27 | The Mead Corporation | Document security system |
| US6340596B1 (en) * | 1998-02-12 | 2002-01-22 | Fujirebio Inc. | Reagent composition for measuring hydrogen sulfide and method for measuring hydrogen sulfide |
Families Citing this family (73)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3718473A (en) * | 1971-01-27 | 1973-02-27 | Du Pont | Photopolymerizable elements containing hydro philic colloids and polymerizable monomers for making gravure printing plate resists |
| US4069056A (en) * | 1974-05-02 | 1978-01-17 | General Electric Company | Photopolymerizable composition containing group Va aromatic onium salts |
| GB1518141A (en) * | 1974-05-02 | 1978-07-19 | Gen Electric | Polymerizable compositions |
| US4264703A (en) * | 1974-05-02 | 1981-04-28 | General Electric Company | Cationically polymerizable compositions containing photodecomposable aromatic iodonium salts |
| US4058400A (en) * | 1974-05-02 | 1977-11-15 | General Electric Company | Cationically polymerizable compositions containing group VIa onium salts |
| US4315998A (en) * | 1974-06-12 | 1982-02-16 | Research Corporation | Polymer-bound photosensitizing catalysts |
| US4307177A (en) * | 1975-12-09 | 1981-12-22 | General Electric Company | Method of using polymerizable compositions containing onium salts |
| US4772541A (en) * | 1985-11-20 | 1988-09-20 | The Mead Corporation | Photohardenable compositions containing a dye borate complex and photosensitive materials employing the same |
| US4937159A (en) * | 1985-11-20 | 1990-06-26 | The Mead Corporation | Photosensitive materials and compositions containing ionic dye compounds as initiators and thiols as autooxidizers |
| US4772530A (en) * | 1986-05-06 | 1988-09-20 | The Mead Corporation | Photosensitive materials containing ionic dye compounds as initiators |
| US4874450A (en) * | 1987-01-29 | 1989-10-17 | The Mead Corporation | Laminating transparent or translucent materials using ionic dye-counter ion complexes |
| US5629354A (en) * | 1995-02-28 | 1997-05-13 | Eastman Kodak Company | Photopolymerization initiator system comprising a spectral sensitizer and a polycarboxylic acid co-initiator |
| US20030087178A1 (en) * | 2001-04-20 | 2003-05-08 | Adrian Lungu | Photopolymerizable element for use as a flexographic printing plate and a process for preparing the plate from the element |
| GB0113121D0 (en) * | 2001-05-30 | 2001-07-18 | Univ Leeds | Biologically active photosensitisers |
| JP2007512297A (ja) * | 2003-11-28 | 2007-05-17 | フォトファーマイカ リミテッド | 生物活性メチレンブルー誘導体（２）における開発 |
| DE102004030019A1 (de) * | 2004-06-22 | 2006-01-19 | Xetos Ag | Photopolymerisierbare Zusammensetzung |
| US20060154180A1 (en) | 2005-01-07 | 2006-07-13 | Kannurpatti Anandkumar R | Imaging element for use as a recording element and process of using the imaging element |
| US7579134B2 (en) * | 2005-03-15 | 2009-08-25 | E. I. Dupont De Nemours And Company | Polyimide composite coverlays and methods and compositions relating thereto |
| US7618766B2 (en) * | 2005-12-21 | 2009-11-17 | E. I. Du Pont De Nemours And Company | Flame retardant photoimagable coverlay compositions and methods relating thereto |
| US7527915B2 (en) * | 2006-07-19 | 2009-05-05 | E. I. Du Pont De Nemours And Company | Flame retardant multi-layer photoimagable coverlay compositions and methods relating thereto |
| WO2008090640A1 (ja) | 2007-01-23 | 2008-07-31 | Fujifilm Corporation | オキシム化合物、感光性組成物、カラーフィルタ及びその製造方法、並びに液晶表示素子 |
| WO2008138732A1 (en) | 2007-05-11 | 2008-11-20 | Basf Se | Oxime ester photoinitiators |
| EP2144876B1 (en) | 2007-05-11 | 2012-09-12 | Basf Se | Oxime ester photoinitiators |
| CN103153952B (zh) | 2010-10-05 | 2016-07-13 | 巴斯夫欧洲公司 | 苯并咔唑化合物的肟酯衍生物及其在可光聚合组合物中作为光敏引发剂的用途 |
| US9051397B2 (en) | 2010-10-05 | 2015-06-09 | Basf Se | Oxime ester |
| WO2013083505A1 (en) | 2011-12-07 | 2013-06-13 | Basf Se | Oxime ester photoinitiators |
| EP2963015B1 (en) | 2012-05-09 | 2018-07-11 | Basf Se | Oxime ester photoinitiators |
| WO2014153158A1 (en) | 2013-03-14 | 2014-09-25 | Icon Health & Fitness, Inc. | Strength training apparatus with flywheel and related methods |
| CN105358527B (zh) | 2013-07-08 | 2018-09-25 | 巴斯夫欧洲公司 | 肟酯光引发剂 |
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| CN105848733B (zh) | 2013-12-26 | 2018-02-13 | 爱康保健健身有限公司 | 缆绳器械中的磁性阻力机构 |
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| US11451108B2 (en) | 2017-08-16 | 2022-09-20 | Ifit Inc. | Systems and methods for axial impact resistance in electric motors |
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-
1967
- 1967-05-23 US US640496A patent/US3579339A/en not_active Expired - Lifetime
-
1968
- 1968-05-08 GB GB21848/68A patent/GB1193923A/en not_active Expired
- 1968-05-14 DE DE1769359A patent/DE1769359C3/de not_active Expired
- 1968-05-22 BE BE715520D patent/BE715520A/xx unknown
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2438672A1 (fr) * | 1978-10-13 | 1980-05-09 | Ciba Geigy Ag | Colorants contenant des groupes amino ou imino |
| US4399209A (en) | 1981-11-12 | 1983-08-16 | The Mead Corporation | Transfer imaging system |
| US4822714A (en) * | 1981-11-12 | 1989-04-18 | The Mead Corporation | Transfer imaging system |
| US4842976A (en) * | 1982-01-18 | 1989-06-27 | Mead Corp. | Color image-forming process |
| US4416966A (en) | 1982-08-25 | 1983-11-22 | The Mead Corporation | Capsular imaging system comprising decolorizing agent |
| US4562137A (en) * | 1982-12-30 | 1985-12-31 | The Mead Corporation | Photosensitive material employing encapsulated radiation sensitive composition |
| GB2133899A (en) * | 1983-01-17 | 1984-08-01 | Mead Corp | Improved imaging system |
| GB2135468A (en) * | 1983-02-15 | 1984-08-30 | Mead Corp | Photosensitive material employing encapsulated radiation sensitive composition and process for improving sensitivity by sequestering oxygen |
| US4482624A (en) * | 1983-02-15 | 1984-11-13 | The Mead Corporation | Photosensitive material employing encapsulated radiation sensitive composition and process for improving sensitivity by sequestering oxygen |
| US4508807A (en) * | 1983-07-11 | 1985-04-02 | Mead Corporation | Photosensitive material employing encapsulated radiation sensitive composition and a transparentizable image-receiving layer |
| US4903991A (en) * | 1983-07-18 | 1990-02-27 | The Mead Corporation | Document security system |
| EP0284938A3 (en) * | 1987-03-28 | 1989-08-30 | Hoechst Aktiengesellschaft | Photopolymerisable composition and registration material prepared therewith |
| EP0287817A3 (en) * | 1987-03-28 | 1989-08-30 | Hoechst Aktiengesellschaft | Photopolymerisable composition and registration material prepared therewith |
| EP0321826A3 (en) * | 1987-12-22 | 1989-08-30 | Hoechst Aktiengesellschaft | Photopolymerisable mixture and recording material manufactured therefrom |
| EP0321827A3 (en) * | 1987-12-22 | 1989-09-06 | Hoechst Aktiengesellschaft | Photopolymerisable mixture and recording material manufactured therefrom |
| US5043249A (en) * | 1987-12-22 | 1991-08-27 | Hoechst Aktiengesellschaft | Photopolymerizable composition comprising (meth)acrylates with photooxidizable groups and a recording material produced therefrom |
| US6340596B1 (en) * | 1998-02-12 | 2002-01-22 | Fujirebio Inc. | Reagent composition for measuring hydrogen sulfide and method for measuring hydrogen sulfide |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1769359A1 (de) | 1971-11-25 |
| DE1769359B2 (de) | 1973-05-30 |
| US3579339A (en) | 1971-05-18 |
| BE715520A (en:Method) | 1968-11-22 |
| DE1769359C3 (de) | 1973-12-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| 429A | Application made for amendment of specification (sect. 29/1949) | ||
| 429H | Application (made) for amendment of specification now open to opposition (sect. 29/1949) | ||
| 429D | Case decided by the comptroller ** specification amended (sect. 29/1949) | ||
| PCNP | Patent ceased through non-payment of renewal fee |