NO154684B - Fremgangsmaate for aa hindre avsetning av damper paa overflaten av en reflektor for en uv-straalingskilde. - Google Patents
Fremgangsmaate for aa hindre avsetning av damper paa overflaten av en reflektor for en uv-straalingskilde. Download PDFInfo
- Publication number
- NO154684B NO154684B NO773792A NO773792A NO154684B NO 154684 B NO154684 B NO 154684B NO 773792 A NO773792 A NO 773792A NO 773792 A NO773792 A NO 773792A NO 154684 B NO154684 B NO 154684B
- Authority
- NO
- Norway
- Prior art keywords
- benzenesulfonyl
- steams
- disposal
- reflector
- hydroxy
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 10
- 230000005855 radiation Effects 0.000 title 1
- 239000002253 acid Substances 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- -1 hydroxybenzenesulfonyl isourea ethers Chemical class 0.000 claims description 6
- 150000007513 acids Chemical class 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 230000003301 hydrolyzing effect Effects 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- JEICAUJOTCALLH-UHFFFAOYSA-N 1-cyclohexyl-3-(4-hydroxyphenyl)sulfonylurea Chemical compound OC1=CC=C(C=C1)S(=O)(=O)NC(=O)NC1CCCCC1 JEICAUJOTCALLH-UHFFFAOYSA-N 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 4
- 239000008280 blood Substances 0.000 description 4
- 210000004369 blood Anatomy 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 206010067125 Liver injury Diseases 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 231100000234 hepatic damage Toxicity 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 230000008818 liver damage Effects 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Chemical compound OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- VDTNNGKXZGSZIP-UHFFFAOYSA-N carbutamide Chemical compound CCCCNC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VDTNNGKXZGSZIP-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 230000000973 chemotherapeutic effect Effects 0.000 description 2
- 210000004185 liver Anatomy 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 125000006239 protecting group Chemical group 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 241000416162 Astragalus gummifer Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229940100389 Sulfonylurea Drugs 0.000 description 1
- JLRGJRBPOGGCBT-UHFFFAOYSA-N Tolbutamide Chemical compound CCCCNC(=O)NS(=O)(=O)C1=CC=C(C)C=C1 JLRGJRBPOGGCBT-UHFFFAOYSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000003385 bacteriostatic effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- WUESWDIHTKHGQA-UHFFFAOYSA-N cyclohexylurea Chemical compound NC(=O)NC1CCCCC1 WUESWDIHTKHGQA-UHFFFAOYSA-N 0.000 description 1
- 239000008298 dragée Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000002443 hepatoprotective effect Effects 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229940078979 liver therapy drug Drugs 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 229960003742 phenol Drugs 0.000 description 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Chemical group O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/06—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation
-
- 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
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F26—DRYING
- F26B—DRYING SOLID MATERIALS OR OBJECTS BY REMOVING LIQUID THEREFROM
- F26B21/00—Arrangements or duct systems, e.g. in combination with pallet boxes, for supplying and controlling air or gases for drying solid materials or objects
- F26B21/14—Arrangements or duct systems, e.g. in combination with pallet boxes, for supplying and controlling air or gases for drying solid materials or objects using gases or vapours other than air or steam, e.g. inert gases
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F26—DRYING
- F26B—DRYING SOLID MATERIALS OR OBJECTS BY REMOVING LIQUID THEREFROM
- F26B3/00—Drying solid materials or objects by processes involving the application of heat
- F26B3/28—Drying solid materials or objects by processes involving the application of heat by radiation, e.g. from the sun
Landscapes
- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Plasma & Fusion (AREA)
- Microbiology (AREA)
- Health & Medical Sciences (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Coating Apparatus (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Arrangement Of Elements, Cooling, Sealing, Or The Like Of Lighting Devices (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
- Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
Description
Fremgangsmåte til fremstilling av terapeutisk virksomme benzolsulfonyl-urinstoffer.
Det er kjent at sulfonylurinstoffer som
N- (4-aminobenzolsulfonyl) -N'-butyl-urinstoff
og N- (4-metyl-benzolsulf onyl) -N'-butyl-urinstoff har en gunstig virkning ved bestemte
leverbeskadigelser. Disse forbindelser fører
imidlertid som likeledes kjent til en sterk ned-settelse av blodsukkerspeilet, dessuten har N-(4-amino-benzolsulfonyl)-N'-butyl-urinstoff
også en i denne sammenheng uønsket bakterio-statisk effekt. Disse forbindelser har derfor
betraktelige ulemper for en vanlig leverterapi.
Det er blitt funnet at hydroksybenzolsulfonyl-urinstoffer med den generelle formel
hvori R betyr cykloalkyl eller cykloalkenyl med 5 til 8 karbonatomer, eller deres salter, har en sterk leverbeskyttelsesvirkning uten å senke blodsukkerspeilet eller å ha en kjemoterapeutisk effekt. Oppfinnelsens gjenstand er fremstillingen av slike hydroksybenzolsulfonyl-urinstoffer. Hertil kan man overføre hydroksybenzol-sulfonylisourinstoffetere med formelen hvori R' betegner alkyl, eller respektive hydroksybenzolsulfonyl-parabansyrer med formel
ved hydrolyse i de ønskede hydroksybenzolsulfonyl-urinstoffer. For fremstilling av de forbindelser som skal underkastes hydrolyse kan man bringe urinstoffderivater som er gjort basiske som isourinstoffetere eller salter av mono-R-substituerte parabansyrer med terti-ære aminer til reaksjon med hydroksybenzol-sulfonylsyrehalogenider.
Ved fremgangsmåten kan de som utgangs-stoffer anvendte m- og p-hydroksybenzolsul-fonylisourinstoffetere, -parabansyrer så vel anvendes i fri form som også i form av forbindelser hvor hydroksygruppen er beskyttet ved en senere avspaltbar rest. Som beskyttelses-gruppe kan det fortrinnsvis anvendes acyl-rester som acetyl, propionyl, benzoyl, alkok-sykarbonylrester som metoksy-karbonyl-, etoksykarbonyl-, benzyloksy-karbonyl-rester, så vel som benzylgrupper. Hvis beskyttelses-gruppen ikke allerede avspaltes under reaksjo-nen kan de fjernes fra de dannede N-(acyl-oksybenzolsulfonyl)- resp. N-(benzyloksy-benzolsulfonyl) -N'-cykloalkyl-urinstoffer eller deres derivater ved hydrolyse med alkalier eller syrer eller fjernes hydrogenolytisk.
Utførelsesformen av fremgangsmåten ifølge oppfinnelsen kan med hensyn til reak-sjonsbetingelser varieres sterkt og tilpasses de herskende forhold. Eksempelvis kan om-setningen foregå under anvendelse av oppløs-ningsmidler ved værelsetemperatur eller ved forhøyet temperatur.
De ved fremgangsmåten ifølge oppfinnelsen dannede benzolsulfonylurinstoffer er p.g.a. deres farmakologiske egenskaper verdifulle legemidler. De nye forbindelser utmerker seg spesielt ved en nekrotrop leverbeskyttelsesvirkning. Den følgende tabell viser for noen av hydrobenzolsulfonyl-urinstoffer fremstillet ifølge oppfinnelsen og som her er anvendt som eksempler, nedsettelsen av allylalkoholens nekrosedannende virkning på rotter. Verdiene ble fastslått ved sammenligning med lever-beskadigelsen av tilsvarende, ikke med N-(4-hydroksy-benzolsulf onyl) -N'-cykloheksyl-urinstoff behandlede kontrolldyr. Målemetoden for leverbeskadigelsene og virkningen av nekrotrope stoffer er beskrevet av W. Eger
(sammenlign Arzneimittelforschung 7, 601
(1957)).
Tilsvarende forbindelser med samme virkning kan også fåes ved fremgangsmåten ifølge patenter nr. 110 341 og 110 343.
Fra tabellen fremgår det at eksempelvis N- (4-hydroksy-benzolsulfonyl) -N'-cyklo-heksyl-urinstoff i en dosering på 50 mg/100 g på rotter nedsetter den nekrosedannende virkning av allylalkoholen i preventivtesten med 65 %. I en dosering på 25 mg/100 g oppnås en nekrotrop virkning av preparatet på omtrent 45 %.
Fremgangsmåteproduktene er spesielt egnet som leverbeskyttelsesstoffer da de enten ikke eller praktisk talt bare forårsaker en ubetydelig blodsukkersenkning og heller ikke har noen kjemoterapeutisk virkning som et sulfonamid. Eksempelvis fører den perorale administrering av 400 mg/kg N-(4-hydroksy-benzolsulfonyl) -N'-cykloheksyl-urinstoff på
kaniner til en senkning av blodsukkerspeilet.
Fremgangsmåteproduktene skal fortrinnsvis anvendes til fremstilling av orale eller parenterale administrerbare preparater med en leverbeskyttelsesvirkning og kan appliseres som sådanne eller i form av salter. Til salt-dannelse kan det eksempelvis anvendes: alka-liske midler, som alkali- eller jordalkali-hydroksyder, -karbonater eller -bikarbonater, videre fysiologisk tålbare organiske baser.
Som medisinske tilberedningsformer kan det anvendes tabletter, kapsler, drageer, opp-løsninger og suspensjoner som inneholder fremgangsmåteproduktene eller deres salter ved siden av de vanlige indifferente bære- og hjelpestoffer som melkesukker, stivelse, gela-tin, magnesiumstearat, planteolje, talkum, tragant, vann o.l.
Eksempel 1.
N- fJi- hydroksy- benzolsulfonylJ-N'- cykloheksyl- urinstoff.
3,5 g 1-(4-hydroksy-benzolsulfonyl)-3-cykloheksyl-parabansyre (smeltepunkt 214— 216°C) blandes med 80 ml ln natronlut og oppvarmes i omtrent 5 minutter på dampbad. Man lar det avkjøle, surgjør svakt, frasuger etter krystallisering og omkrystalliserer reak-sjonsproduktet fra fortynnet metanol. N-(4-hydroksy-benzolsulfonyl)-N'-cykloheksyl-urinstoff smelter ved 192 til 194°C.
På analog måte vil man av l-( 4-hydroksy-benzolsulfonyl)-3-cykloheksenylparabansyre få N-(4-hydroksy-benzolsulfonyl)-N'-(A<3->eyklohekseny])-urinstoff, som etter omkry-stallisering fra etanol og god tørkning ved 120°C smelter ved 166—168°C.
Eksempel 2.
N-( Jf- hydroksy- benzolsulfonyl)-N'~ cykloheksyl- urinstoff.
3,1 g N-(4-hydroksy-benzolsulfonyl) -N'-cykloheksyl-isourinstoff-metyleter (smeltepunkt 142—144°C) oppvarmes på dampbad med 10 ml konsentrert saltsyre inntil gass-utviklingen er avsluttet. Man lar det avkjøle noe, blander med vann og frasuger reaksjons-produktet. Stoffet omfelles fra 1%-ig ammo-niakk og omkrystalliseres fra metanol. Det således dannede N-( 4-hydroksy-benzolsulfonyl)-N'-cykloheksyl-urinstoff smelter ved 192 til 194°C.
Claims (1)
- Fremgangsmåte til fremstilling av terapeutisk virksomme benzolsulfonyl-urinstoffer med den generelle formelhvori R betyr cykloalkyl, eller cykloalkenyl med 5 til 8 karbonatomer, eller deres salter,karakterisert ved at man hydroly-serer R-substituerte hydroksybenzolsulfonyl-isourinstoffetere med formel hvori R' betegner alkyl, eller hydroksybenzolsulfonyl-parabansyrer med formel og overfører de dannede produkter eventuelt ved hjelp av baser i de tilsvarende salter.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/739,120 US4135098A (en) | 1976-11-05 | 1976-11-05 | Method and apparatus for curing coating materials |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO773792L NO773792L (no) | 1978-05-08 |
| NO154684B true NO154684B (no) | 1986-08-25 |
| NO154684C NO154684C (no) | 1986-12-03 |
Family
ID=24970908
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO773792A NO154684C (no) | 1976-11-05 | 1977-11-04 | Fremgangsmaate for aa hindre avsetning av damper paa overflaten av en reflektor for en uv-straalingskilde. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US4135098A (no) |
| JP (1) | JPS5363786A (no) |
| AU (1) | AU511287B2 (no) |
| BE (1) | BE860509A (no) |
| CA (1) | CA1100904A (no) |
| DE (1) | DE2749439C3 (no) |
| DK (1) | DK492377A (no) |
| ES (2) | ES463846A1 (no) |
| FR (1) | FR2370071A1 (no) |
| GB (1) | GB1591442A (no) |
| IT (1) | IT1090430B (no) |
| NL (1) | NL7712191A (no) |
| NO (1) | NO154684C (no) |
| SE (1) | SE438107B (no) |
| SU (1) | SU803851A3 (no) |
| ZA (1) | ZA776207B (no) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1980001558A1 (en) * | 1979-01-29 | 1980-08-07 | K Taniuchi | Easy-to-open lid for container |
| US4331705A (en) * | 1979-05-11 | 1982-05-25 | Minnesota Mining And Manufacturing Company | Curing of polyamic acids or salts thereof by ultraviolet exposure |
| DE3010821A1 (de) * | 1980-03-21 | 1981-10-01 | Polymer-Physik GmbH & Co KG, 2844 Lemförde | Verfahren und vorrichtung zur vernetzung von auf traegermaterialien aufgebrachten lacken auf kunststoffbasis |
| DE3402505A1 (de) * | 1983-01-25 | 1984-08-09 | Citizen Watch Co. Ltd., Tanashi, Tokyo | Vorrichtung und verfahren zum aushaerten von unter lichteinwirkung aushaertenden kunstharzklebern |
| FR2544324B1 (fr) * | 1983-04-13 | 1987-07-10 | Toyo Boseki | Procede pour accroitre l'adherence de la surface d'un produit faconne en polyester et produit obtenu par ce procede |
| DE3416502A1 (de) * | 1984-05-04 | 1985-11-07 | Goldschmidt Ag Th | Vorrichtung zum aushaerten von flaechigen werkstoffen aus durch uv-strahlung haertbaren verbindungen oder zubereitungen |
| US4660297A (en) * | 1985-11-01 | 1987-04-28 | Philip Danielson | Desorption of water molecules in a vacuum system using ultraviolet radiation |
| JPS63158166A (ja) * | 1986-12-23 | 1988-07-01 | Fuji Photo Film Co Ltd | 帯状物の乾燥方法 |
| US4798007A (en) * | 1987-05-28 | 1989-01-17 | Eichenlaub John E | Explosion-proof, pollution-free infrared dryer |
| US4811493A (en) * | 1987-08-05 | 1989-03-14 | Burgio Joseph T Jr | Dryer-cooler apparatus |
| US4823680A (en) * | 1987-12-07 | 1989-04-25 | Union Carbide Corporation | Wide laminar fluid doors |
| US5225170A (en) * | 1989-02-07 | 1993-07-06 | Steelcase Inc. | Monolithic finishing process and machine for furniture parts and the like |
| US5116639A (en) * | 1989-02-07 | 1992-05-26 | Steelcase Inc. | Monolithic finishing process and machine for furniture parts and the like |
| JPH0390319A (ja) * | 1989-09-01 | 1991-04-16 | Sogo Shika Iryo Kenkyusho:Kk | 可視光重合型レジンの連続硬化方法及び装置 |
| DE4431502A1 (de) * | 1994-09-03 | 1996-03-07 | Atotech Deutschland Gmbh | Verfahren zur mehrschichtigen Oberflächenbehandlung von Werkstücken aus Kunststoff in Tauchbadanlagen |
| DE19516053C2 (de) * | 1995-05-04 | 2000-08-24 | Ist Metz Gmbh | UV-Strahler |
| CA2220108A1 (en) * | 1995-05-04 | 1996-11-07 | Nolle Gmbh | Apparatus for hardening a layer on a substrate |
| US6126095A (en) * | 1998-09-09 | 2000-10-03 | Fusion Uv Systems, Inc. | Ultraviolet curing apparatus using an inert atmosphere chamber |
| US6755518B2 (en) * | 2001-08-30 | 2004-06-29 | L&P Property Management Company | Method and apparatus for ink jet printing on rigid panels |
| DE10238253B4 (de) * | 2002-08-21 | 2007-12-13 | Advanced Photonics Technologies Ag | UV-Bestrahlungsanlage zur Erzeugung eines ausgedehnten UV-Strahlungsfeldes |
| FR2865418B1 (fr) * | 2004-01-28 | 2006-03-03 | Air Liquide | Equipement de reticulation ultraviolette sous atmosphere controlee |
| US20050250346A1 (en) * | 2004-05-06 | 2005-11-10 | Applied Materials, Inc. | Process and apparatus for post deposition treatment of low k dielectric materials |
| DE102005000837B4 (de) * | 2005-01-05 | 2022-03-31 | Advanced Photonics Technologies Ag | Thermische Bestrahlungsanordnung zur Erwärmung eines Bestrahlungsgutes |
| US7777198B2 (en) | 2005-05-09 | 2010-08-17 | Applied Materials, Inc. | Apparatus and method for exposing a substrate to a rotating irradiance pattern of UV radiation |
| US20060251827A1 (en) * | 2005-05-09 | 2006-11-09 | Applied Materials, Inc. | Tandem uv chamber for curing dielectric materials |
| SG136078A1 (en) * | 2006-03-17 | 2007-10-29 | Applied Materials Inc | Uv cure system |
| US7566891B2 (en) * | 2006-03-17 | 2009-07-28 | Applied Materials, Inc. | Apparatus and method for treating a substrate with UV radiation using primary and secondary reflectors |
| US7692171B2 (en) * | 2006-03-17 | 2010-04-06 | Andrzei Kaszuba | Apparatus and method for exposing a substrate to UV radiation using asymmetric reflectors |
| JP5976776B2 (ja) | 2011-04-08 | 2016-08-24 | アプライド マテリアルズ インコーポレイテッドＡｐｐｌｉｅｄ Ｍａｔｅｒｉａｌｓ，Ｉｎｃｏｒｐｏｒａｔｅｄ | Ｕｖ処理、化学処理、および堆積のための装置および方法 |
| DE102015219239A1 (de) * | 2015-10-06 | 2017-04-06 | Reicolor Chemie-Gmbh Chemische- Und Lackfabrik | Verfahren zum Lackieren von Stiften sowie Lackiervorrichtung |
| WO2020022424A1 (ja) * | 2018-07-27 | 2020-01-30 | 京セラ株式会社 | 光照射装置および印刷装置 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR761815A (fr) * | 1932-12-20 | 1934-03-28 | Vitamina | Perfectionnements aux appareils à stériliser par rayons ultra-violets |
| GB715700A (en) * | 1951-10-12 | 1954-09-22 | English Electric Co Ltd | Improvements relating to control apparatus for electric motors |
| NL261714A (no) * | 1960-06-14 | |||
| GB991561A (en) * | 1961-03-20 | 1965-05-12 | Ford Motor Co | Improvements in coatings of compositions comprising a polyester |
| DE2018984A1 (de) * | 1969-04-23 | 1971-06-24 | British Insulated Callenders | Verfahren und Einrichtung zum Aus harten von Isolationsuberzugen auf elek tnschen Leitern |
| US3807052A (en) * | 1972-06-26 | 1974-04-30 | Union Carbide Corp | Apparatus for irradiation of a moving product in an inert atmosphere |
| US3790801A (en) * | 1972-09-08 | 1974-02-05 | Ppg Industries Inc | Apparatus for ultraviolet light treatment in a controlled atmosphere |
| US3826014A (en) * | 1973-03-19 | 1974-07-30 | Sun Chemical Corp | Shutter mechanism for radiation-curing lamp |
| BR7404245A (pt) * | 1973-05-25 | 1976-02-03 | Union Carbide Corp | Processo de fabricacao de amterial de cobertura de pisos |
| US3819929A (en) * | 1973-06-08 | 1974-06-25 | Canrad Precision Ind Inc | Ultraviolet lamp housing |
| JPS5241370B2 (no) * | 1973-09-14 | 1977-10-18 | ||
| US3936950A (en) * | 1974-04-16 | 1976-02-10 | Union Carbide Corporation | Method of inerting the atmosphere above a moving product |
| CA1045580A (en) * | 1974-04-16 | 1979-01-02 | Harden H. Troue | Method of inerting the atmosphere above a moving product |
| US4005135A (en) * | 1975-04-07 | 1977-01-25 | Sun Chemical Corporation | Rotatable ultraviolet lamp reflector and heat sink |
| US3994073A (en) * | 1975-04-08 | 1976-11-30 | Ppg Industries, Inc. | Air cooling means for UV processor |
-
1976
- 1976-11-05 US US05/739,120 patent/US4135098A/en not_active Expired - Lifetime
-
1977
- 1977-10-18 ZA ZA00776207A patent/ZA776207B/xx unknown
- 1977-10-26 CA CA289,543A patent/CA1100904A/en not_active Expired
- 1977-11-04 NL NL7712191A patent/NL7712191A/xx not_active Application Discontinuation
- 1977-11-04 SE SE7712490A patent/SE438107B/sv not_active IP Right Cessation
- 1977-11-04 BE BE182369A patent/BE860509A/xx not_active IP Right Cessation
- 1977-11-04 SU SU772542048A patent/SU803851A3/ru active
- 1977-11-04 DK DK492377A patent/DK492377A/da not_active Application Discontinuation
- 1977-11-04 JP JP13163877A patent/JPS5363786A/ja active Granted
- 1977-11-04 FR FR7733243A patent/FR2370071A1/fr active Granted
- 1977-11-04 ES ES463846A patent/ES463846A1/es not_active Expired
- 1977-11-04 AU AU30331/77A patent/AU511287B2/en not_active Expired
- 1977-11-04 IT IT51697/77A patent/IT1090430B/it active
- 1977-11-04 NO NO773792A patent/NO154684C/no unknown
- 1977-11-04 DE DE2749439A patent/DE2749439C3/de not_active Expired
- 1977-11-04 GB GB45903/77A patent/GB1591442A/en not_active Expired
- 1977-12-14 ES ES465054A patent/ES465054A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| ZA776207B (en) | 1978-06-28 |
| DE2749439C3 (de) | 1980-10-16 |
| NO773792L (no) | 1978-05-08 |
| FR2370071A1 (fr) | 1978-06-02 |
| CA1100904A (en) | 1981-05-12 |
| US4135098A (en) | 1979-01-16 |
| ES463846A1 (es) | 1978-06-16 |
| SE438107B (sv) | 1985-04-01 |
| AU511287B2 (en) | 1980-08-07 |
| DE2749439B2 (de) | 1980-02-28 |
| BE860509A (fr) | 1978-05-05 |
| IT1090430B (it) | 1985-06-26 |
| ES465054A1 (es) | 1978-09-01 |
| JPS5537949B2 (no) | 1980-10-01 |
| NO154684C (no) | 1986-12-03 |
| NL7712191A (nl) | 1978-05-09 |
| SE7712490L (sv) | 1978-05-06 |
| SU803851A3 (ru) | 1981-02-07 |
| DE2749439A1 (de) | 1978-05-11 |
| JPS5363786A (en) | 1978-06-07 |
| DK492377A (da) | 1978-05-06 |
| AU3033177A (en) | 1979-05-10 |
| FR2370071B1 (no) | 1983-02-25 |
| GB1591442A (en) | 1981-06-24 |
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