BE402381A - - Google Patents
Info
- Publication number
- BE402381A BE402381A BE402381DA BE402381A BE 402381 A BE402381 A BE 402381A BE 402381D A BE402381D A BE 402381DA BE 402381 A BE402381 A BE 402381A
- Authority
- BE
- Belgium
- Prior art keywords
- product
- das
- desc
- clms page
- page number
- Prior art date
Links
- 239000012530 fluid Substances 0.000 claims description 3
- 239000000314 lubricant Substances 0.000 claims description 2
- 125000001475 halogen functional group Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000047 product Substances 0.000 description 39
- 239000007788 liquid Substances 0.000 description 20
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 14
- 239000000460 chlorine Substances 0.000 description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 9
- 229910052801 chlorine Inorganic materials 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000007789 gas Substances 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 239000012212 insulator Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000005660 chlorination reaction Methods 0.000 description 3
- 239000002360 explosive Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- SUBDBMMJDZJVOS-UHFFFAOYSA-N 5-methoxy-2-{[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl}-1H-benzimidazole Chemical compound N=1C2=CC(OC)=CC=C2NC=1S(=O)CC1=NC=C(C)C(OC)=C1C SUBDBMMJDZJVOS-UHFFFAOYSA-N 0.000 description 2
- 206010010071 Coma Diseases 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- XEMRAKSQROQPBR-UHFFFAOYSA-N (trichloromethyl)benzene Chemical class ClC(Cl)(Cl)C1=CC=CC=C1 XEMRAKSQROQPBR-UHFFFAOYSA-N 0.000 description 1
- NUMXHEUHHRTBQT-AATRIKPKSA-N 2,4-dimethoxy-1-[(e)-2-nitroethenyl]benzene Chemical compound COC1=CC=C(\C=C\[N+]([O-])=O)C(OC)=C1 NUMXHEUHHRTBQT-AATRIKPKSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 241000534414 Anotopterus nikparini Species 0.000 description 1
- 241001338801 Chlorus Species 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 241001550206 Colla Species 0.000 description 1
- 241000156867 Cryptodacus tau Species 0.000 description 1
- 241001268392 Dalla Species 0.000 description 1
- 241000283014 Dama Species 0.000 description 1
- 241001397104 Dima Species 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- 101100400378 Mus musculus Marveld2 gene Proteins 0.000 description 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
- 101100370014 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) tof-1 gene Proteins 0.000 description 1
- -1 Or-r on a Proteins 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241001674048 Phthiraptera Species 0.000 description 1
- 241000497192 Phyllocoptruta oleivora Species 0.000 description 1
- 241001377010 Pila Species 0.000 description 1
- 241000549435 Pria Species 0.000 description 1
- 241000655872 Puia Species 0.000 description 1
- 241001014642 Rasta Species 0.000 description 1
- 241000283984 Rodentia Species 0.000 description 1
- 241000124033 Salix Species 0.000 description 1
- 241000162337 Stolas Species 0.000 description 1
- 101150007604 TRIM44 gene Proteins 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 241001125929 Trisopterus luscus Species 0.000 description 1
- 244000245420 ail Species 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- JNSGIVNNHKGGRU-JYRVWZFOSA-N diethoxyphosphinothioyl (2z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetate Chemical compound CCOP(=S)(OCC)OC(=O)C(=N/OC)\C1=CSC(N)=N1 JNSGIVNNHKGGRU-JYRVWZFOSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 101150016902 dltC gene Proteins 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229940096118 ella Drugs 0.000 description 1
- 235000004611 garlic Nutrition 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- MFZOSKPPVCIFMT-UHFFFAOYSA-N pinazepam Chemical compound C12=CC(Cl)=CC=C2N(CC#C)C(=O)CN=C1C1=CC=CC=C1 MFZOSKPPVCIFMT-UHFFFAOYSA-N 0.000 description 1
- 101150002764 purA gene Proteins 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000012262 resinous product Substances 0.000 description 1
- 230000035943 smell Effects 0.000 description 1
- 210000004722 stifle Anatomy 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- OOLLAFOLCSJHRE-ZHAKMVSLSA-N ulipristal acetate Chemical compound C1=CC(N(C)C)=CC=C1[C@@H]1C2=C3CCC(=O)C=C3CC[C@H]2[C@H](CC[C@]2(OC(C)=O)C(C)=O)[C@]2(C)C1 OOLLAFOLCSJHRE-ZHAKMVSLSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G4/00—Fixed capacitors; Processes of their manufacture
- H01G4/002—Details
- H01G4/018—Dielectrics
- H01G4/20—Dielectrics using combinations of dielectrics from more than one of groups H01G4/02 - H01G4/06
- H01G4/22—Dielectrics using combinations of dielectrics from more than one of groups H01G4/02 - H01G4/06 impregnated
- H01G4/221—Dielectrics using combinations of dielectrics from more than one of groups H01G4/02 - H01G4/06 impregnated characterised by the composition of the impregnant
- H01G4/222—Dielectrics using combinations of dielectrics from more than one of groups H01G4/02 - H01G4/06 impregnated characterised by the composition of the impregnant halogenated
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/20—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances liquids, e.g. oils
- H01B3/24—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances liquids, e.g. oils containing halogen in the molecules, e.g. halogenated oils
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE402381A true BE402381A (esLanguage) |
Family
ID=68165
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE402381D BE402381A (esLanguage) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE402381A (esLanguage) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2312841A1 (fr) * | 1975-05-30 | 1976-12-24 | Monsanto Co | Dispositifs electriques contenant des fluides dielectriques facilement biodegradables, a base de composes de diphenylmethane halogene |
| EP0008251A1 (fr) * | 1978-07-27 | 1980-02-20 | P C U K Produits Chimiques Ugine Kuhlmann | Nouveaux diélectriques liquides, procédé de préparation et applications |
| FR2432199A1 (fr) * | 1978-07-27 | 1980-02-22 | Ugine Kuhlmann | Nouveaux dielectriques liquides |
| FR2449954A2 (fr) * | 1979-02-20 | 1980-09-19 | Ugine Kuhlmann | Nouveaux fluides isolants pour transformateurs |
-
0
- BE BE402381D patent/BE402381A/fr unknown
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2312841A1 (fr) * | 1975-05-30 | 1976-12-24 | Monsanto Co | Dispositifs electriques contenant des fluides dielectriques facilement biodegradables, a base de composes de diphenylmethane halogene |
| EP0008251A1 (fr) * | 1978-07-27 | 1980-02-20 | P C U K Produits Chimiques Ugine Kuhlmann | Nouveaux diélectriques liquides, procédé de préparation et applications |
| FR2432199A1 (fr) * | 1978-07-27 | 1980-02-22 | Ugine Kuhlmann | Nouveaux dielectriques liquides |
| FR2449954A2 (fr) * | 1979-02-20 | 1980-09-19 | Ugine Kuhlmann | Nouveaux fluides isolants pour transformateurs |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN102260551B (zh) | 用于液态烃以及其它的燃料和油的标记化合物 | |
| Pang et al. | Structure and thermal properties of β-sitosterol-beeswax-sunflower oleogels | |
| Takeuchi et al. | Crystallization kinetics of polymorphic forms of a molecular compound constructed by SOS (1, 3-distearoyl-2-oleoyl-sn-glycerol) and SSO (1, 2-distearoyl-3-oleoyl-rac-glycerol) | |
| Kitching et al. | Further studies of substitution reactions of stannyl and germyl anionoids with alkyl bromides. Rearrangement of the 6-hepten-2-yl moiety | |
| AR004365A1 (es) | Composiciones de solventes parafinicos de alta pureza y procedimiento para produccion | |
| CN1703499A (zh) | 用作重质润滑剂基础原料的重质烃组合物 | |
| BE402381A (esLanguage) | ||
| Shuai et al. | Effect of different oleogelation mechanisms on physical properties and oxidative stability of macadamia oil-based oleogels and its application | |
| Garin et al. | Enhancement of optical activity by fractional sublimation. An alternative to fractional crystallization and a warning | |
| CN107325838B (zh) | 一种费托合成粗产品的分离方法 | |
| Arrieira et al. | Oleogels based on carotenoid-rich microbial oil produced by R. mucilaginosa in agro-industrial by-products | |
| JPS5876497A (ja) | 安定性にすぐれた冷凍機油 | |
| Barton et al. | trans-α, α, α′, α′-Tetraphenyl-9, 10-dihydro-9, 10-ethanoanthracene-11, 12-dimethanol and its tetra (p-chlorophenyl) derivative: roof-shaped host compounds for the purification of aromatic C8H10 isomeric guest mixtures | |
| US4041086A (en) | Process of manufacture of flourinated alkyladamantanes | |
| DE69418675T2 (de) | Eine Silacyclohexanverbindung, deren Herstellung und diese enthaltende Flüssigkristallzusammensetzung | |
| Sadgrove et al. | Dihydrotagetone, an unusual fruity ketone, is found in enantiopure and enantioenriched forms in additional Australian native taxa of Phebalium (Rutaceae: Boronieae) | |
| EP0008251A1 (fr) | Nouveaux diélectriques liquides, procédé de préparation et applications | |
| Zaky et al. | Separation of some paraffin wax grades using solvent extraction technique | |
| Kamijo et al. | Polymorphic structure of dl-12hydroxystearic acid | |
| EP0500435B1 (fr) | Utilisation d'isomères de mono et bis(méthylbenzyle)xylène comme fluide de transfert thermique | |
| US2071521A (en) | Production of fluorescence producing substances soluble in hydrocarbon oils | |
| Tecklenburg et al. | Effect of copper on the local structure of GeSe2Cux probed by Raman spectroscopy | |
| US2111126A (en) | Substances producing fluorescence | |
| AU764202B2 (en) | Trialkylmethane mixtures as synthetic lubricants | |
| DE556309C (de) | Verfahren zur Gewinnung von Schmieroelen |