GB1357681A - Process for carrying out sensitised photo-chemical reactions - Google Patents
Process for carrying out sensitised photo-chemical reactionsInfo
- Publication number
- GB1357681A GB1357681A GB1195072A GB1195072A GB1357681A GB 1357681 A GB1357681 A GB 1357681A GB 1195072 A GB1195072 A GB 1195072A GB 1195072 A GB1195072 A GB 1195072A GB 1357681 A GB1357681 A GB 1357681A
- Authority
- GB
- United Kingdom
- Prior art keywords
- tube
- anhydride
- layer
- sensitizer
- coated
- 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
- 238000000034 method Methods 0.000 title abstract 3
- 238000006552 photochemical reaction Methods 0.000 title 1
- 239000000463 material Substances 0.000 abstract 5
- 239000003504 photosensitizing agent Substances 0.000 abstract 4
- KUIZKZHDMPERHR-UHFFFAOYSA-N 1-phenylprop-2-en-1-one Chemical compound C=CC(=O)C1=CC=CC=C1 KUIZKZHDMPERHR-UHFFFAOYSA-N 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- 229920001577 copolymer Polymers 0.000 abstract 3
- 239000007791 liquid phase Substances 0.000 abstract 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- 230000001678 irradiating effect Effects 0.000 abstract 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 abstract 2
- 239000000376 reactant Substances 0.000 abstract 2
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 abstract 1
- PMJHHCWVYXUKFD-PLNGDYQASA-N (3z)-penta-1,3-diene Chemical compound C\C=C/C=C PMJHHCWVYXUKFD-PLNGDYQASA-N 0.000 abstract 1
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 abstract 1
- AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 abstract 1
- LYWRIGIFLAVWAF-UHFFFAOYSA-N 2-benzothiophene-1,3-dione Chemical compound C1=CC=C2C(=O)SC(=O)C2=C1 LYWRIGIFLAVWAF-UHFFFAOYSA-N 0.000 abstract 1
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 abstract 1
- NYLPCWOBCQLPTP-UHFFFAOYSA-N 6,7-dimethyl-3-oxabicyclo[3.2.0]hept-6-ene-2,4-dione Chemical compound CC=1C2C(C1C)C(=O)OC2=O NYLPCWOBCQLPTP-UHFFFAOYSA-N 0.000 abstract 1
- MMNWSHJJPDXKCH-UHFFFAOYSA-N 9,10-dioxoanthracene-2-sulfonic acid Chemical compound C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 MMNWSHJJPDXKCH-UHFFFAOYSA-N 0.000 abstract 1
- 239000004593 Epoxy Substances 0.000 abstract 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 abstract 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 abstract 1
- 239000004642 Polyimide Substances 0.000 abstract 1
- JUWYWJJNDLGYCT-UHFFFAOYSA-N ac1l9nv8 Chemical compound C12=CC=CC=C2C2C=C(C(=O)OC)C1C1=CC=CC=C12 JUWYWJJNDLGYCT-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- JRPRCOLKIYRSNH-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OCC2OC2)C=1C(=O)OCC1CO1 JRPRCOLKIYRSNH-UHFFFAOYSA-N 0.000 abstract 1
- NEPKLUNSRVEBIX-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) benzene-1,4-dicarboxylate Chemical compound C=1C=C(C(=O)OCC2OC2)C=CC=1C(=O)OCC1CO1 NEPKLUNSRVEBIX-UHFFFAOYSA-N 0.000 abstract 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 238000001704 evaporation Methods 0.000 abstract 1
- ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000011521 glass Substances 0.000 abstract 1
- 239000008187 granular material Substances 0.000 abstract 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 abstract 1
- 238000011065 in-situ storage Methods 0.000 abstract 1
- 229940087305 limonene Drugs 0.000 abstract 1
- 235000001510 limonene Nutrition 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 abstract 1
- 229910052753 mercury Inorganic materials 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 abstract 1
- 229920001721 polyimide Polymers 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 229930187593 rose bengal Natural products 0.000 abstract 1
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 abstract 1
- 238000010792 warming Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F16/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
- C08F16/36—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by a ketonic radical
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/08—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
- B01J19/12—Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electromagnetic waves
- B01J19/122—Incoherent waves
- B01J19/123—Ultraviolet light
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH386271A CH544573A (de) | 1971-03-16 | 1971-03-16 | Verfahren zur Durchführung sensibilisierter photochemischer Reaktionen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1357681A true GB1357681A (en) | 1974-06-26 |
Family
ID=4265063
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1195072A Expired GB1357681A (en) | 1971-03-16 | 1972-03-15 | Process for carrying out sensitised photo-chemical reactions |
Country Status (5)
| Country | Link |
|---|---|
| CH (1) | CH544573A (xx) |
| DE (1) | DE2210108B2 (xx) |
| FR (1) | FR2130248B1 (xx) |
| GB (1) | GB1357681A (xx) |
| NL (1) | NL7203444A (xx) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55115484A (en) * | 1979-02-28 | 1980-09-05 | Asahi Chem Ind Co Ltd | Heterogeneous sensitizer for photosensitized oxidation |
| CN113185380A (zh) * | 2020-01-14 | 2021-07-30 | 浙江九洲药业股份有限公司 | 一种绿色光氧化连续制备大麻二酚中间体的方法 |
| CN117000216B (zh) * | 2023-10-07 | 2023-12-08 | 国能龙源环保有限公司 | 螯合剂、燃煤电厂脱硫废水的工业化处理系统及处理方法 |
-
1971
- 1971-03-16 CH CH386271A patent/CH544573A/de not_active IP Right Cessation
-
1972
- 1972-03-02 DE DE19722210108 patent/DE2210108B2/de active Pending
- 1972-03-15 GB GB1195072A patent/GB1357681A/en not_active Expired
- 1972-03-15 FR FR7208956A patent/FR2130248B1/fr not_active Expired
- 1972-03-15 NL NL7203444A patent/NL7203444A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE2210108A1 (de) | 1972-10-05 |
| FR2130248A1 (xx) | 1972-11-03 |
| FR2130248B1 (xx) | 1974-06-28 |
| DE2210108B2 (de) | 1973-05-24 |
| NL7203444A (xx) | 1972-09-19 |
| CH544573A (de) | 1973-11-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2722512A (en) | Photopolymerization process | |
| US3586616A (en) | Bis(perfluoroalkylsulfonyl)methane metal salts in cationic polymerization | |
| US4058400A (en) | Cationically polymerizable compositions containing group VIa onium salts | |
| US4161405A (en) | Method of cationally polymerizing oxirane free materials with group VIa onium salts | |
| EP0195846B1 (en) | Photo-curable epoxy resin type composition and curing process | |
| BRADY | Halogenated Ketenes: Valuable Intermediates in Organic Synthesis1 | |
| GB1566114A (en) | Radiation curable unsaturated addition products for coatings | |
| JPH09500921A (ja) | 重合用触媒および開始剤 | |
| JPS5812913B2 (ja) | クウキカンソウヒフクソセイブツ オヨビ ソノセイゾウホウホウ | |
| GB1357681A (en) | Process for carrying out sensitised photo-chemical reactions | |
| EP0003908B1 (en) | Chemical process in a medium connected to a rotating body | |
| US3932557A (en) | Reactive hydrophilic epoxy containing polymer | |
| GB843543A (en) | Improved photomechanical printing processes | |
| US2548685A (en) | Photopolymerization process and compositions | |
| US3888912A (en) | Process for making beta-acryloyloxypropanoic acid | |
| US4398013A (en) | Accelerator for anhydride-cured epoxy resins | |
| Hayase et al. | Photopolymerization of epoxides. A new type of photopolymerization with photodecomposable silyl ether as coinitiator | |
| JPS6015650B2 (ja) | 光重合性組成物 | |
| Burlant et al. | Effect of Radiation on P0lyacrylonitrile and Poly-α-methaerylonitrile | |
| Crivello et al. | The synthesis and characterization of polymer-bound diaryliodonium salts and their use in photo and thermally initiated cationic polymerization | |
| US5354784A (en) | Cyclopentadienyliron complex salt, process for preparing the same and photopolymerizable composition containing the same | |
| US3826784A (en) | Novel reactive cinnamate polymers | |
| US3563741A (en) | Photopolymerisation of ethylenically unsaturated organic compounds | |
| JPH0672955A (ja) | 活性エネルギー線硬化樹脂用反応性希釈剤及びその 製造法 | |
| JPS5851008B2 (ja) | グラフトキヨウジユウゴウタイノ セイゾウホウ |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |