DE2210108B2 - Verfahren zur durchfuehrung sensibilisierter photoreaktionen und die verwendung von unloeslichen sensibilisatoren zur durchfuehrung sensibilisierter photoreaktionen - Google Patents
Verfahren zur durchfuehrung sensibilisierter photoreaktionen und die verwendung von unloeslichen sensibilisatoren zur durchfuehrung sensibilisierter photoreaktionenInfo
- Publication number
- DE2210108B2 DE2210108B2 DE19722210108 DE2210108A DE2210108B2 DE 2210108 B2 DE2210108 B2 DE 2210108B2 DE 19722210108 DE19722210108 DE 19722210108 DE 2210108 A DE2210108 A DE 2210108A DE 2210108 B2 DE2210108 B2 DE 2210108B2
- Authority
- DE
- Germany
- Prior art keywords
- photoreactions
- insoluble
- sensitizer
- sensitized
- phase
- 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.)
- Pending
Links
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- 150000001789 chalcones Chemical class 0.000 description 1
- 235000005513 chalcones Nutrition 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- RCTYPNKXASFOBE-UHFFFAOYSA-M chloromercury Chemical compound [Hg]Cl RCTYPNKXASFOBE-UHFFFAOYSA-M 0.000 description 1
- 150000001868 cobalt Chemical class 0.000 description 1
- JAWGVVJVYSANRY-UHFFFAOYSA-N cobalt(3+) Chemical compound [Co+3] JAWGVVJVYSANRY-UHFFFAOYSA-N 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 238000002474 experimental method Methods 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
- 230000006870 function Effects 0.000 description 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 description 1
- 239000007789 gas Substances 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 125000003010 ionic group Chemical group 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000002950 monocyclic group Chemical class 0.000 description 1
- 150000002829 nitrogen Chemical class 0.000 description 1
- 229910052756 noble gas Inorganic materials 0.000 description 1
- 150000002835 noble gases Chemical class 0.000 description 1
- 238000006552 photochemical reaction Methods 0.000 description 1
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 125000003367 polycyclic group Chemical class 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920001290 polyvinyl ester Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- KRIOVPPHQSLHCZ-UHFFFAOYSA-N propiophenone Chemical compound CCC(=O)C1=CC=CC=C1 KRIOVPPHQSLHCZ-UHFFFAOYSA-N 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- GGCZERPQGJTIQP-UHFFFAOYSA-M sodium 2-anthraquinonesulfonate Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)[O-])=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000003455 sulfinic acids Chemical class 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 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)
- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (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 (2)
| Publication Number | Publication Date |
|---|---|
| DE2210108A1 DE2210108A1 (de) | 1972-10-05 |
| DE2210108B2 true DE2210108B2 (de) | 1973-05-24 |
Family
ID=4265063
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19722210108 Pending DE2210108B2 (de) | 1971-03-16 | 1972-03-02 | Verfahren zur durchfuehrung sensibilisierter photoreaktionen und die verwendung von unloeslichen sensibilisatoren zur durchfuehrung sensibilisierter photoreaktionen |
Country Status (5)
| Country | Link |
|---|---|
| CH (1) | CH544573A (enExample) |
| DE (1) | DE2210108B2 (enExample) |
| FR (1) | FR2130248B1 (enExample) |
| GB (1) | GB1357681A (enExample) |
| NL (1) | NL7203444A (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3006886A1 (de) * | 1979-02-28 | 1980-09-11 | Asahi Dow Ltd | Verfahren zur photooxidation durch sichtbares licht unter verwendung eines sensibilisators, die sensibilisatoren und vorrichtung zur durchfuehrung des verfahrens |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113185380B (zh) * | 2020-01-14 | 2024-12-10 | 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 NL NL7203444A patent/NL7203444A/xx unknown
- 1972-03-15 FR FR7208956A patent/FR2130248B1/fr not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3006886A1 (de) * | 1979-02-28 | 1980-09-11 | Asahi Dow Ltd | Verfahren zur photooxidation durch sichtbares licht unter verwendung eines sensibilisators, die sensibilisatoren und vorrichtung zur durchfuehrung des verfahrens |
| DE3049701C1 (de) * | 1979-02-28 | 1985-07-11 | Asahi Chemical Ind | Sensibilisator zur Photooxidation durch sichtbares Licht und Sauerstoff |
Also Published As
| Publication number | Publication date |
|---|---|
| NL7203444A (enExample) | 1972-09-19 |
| FR2130248B1 (enExample) | 1974-06-28 |
| GB1357681A (en) | 1974-06-26 |
| FR2130248A1 (enExample) | 1972-11-03 |
| CH544573A (de) | 1973-11-30 |
| DE2210108A1 (de) | 1972-10-05 |
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