FI78499C - Svaorantaendlig, biologiskt soenderfallande funktionell vaetska. - Google Patents

Svaorantaendlig, biologiskt soenderfallande funktionell vaetska. Download PDF

Info

Publication number: FI78499C
Authority: FI; Finland
Prior art keywords: brominated; benzyltoluene; derivatives; biodegradable; dibromobenzyltoluene
Prior art date: 1984-01-27

Application number

FI853708A

Other languages

English (en)

Finnish (fi)

Swedish (sv)

Other versions

FI853708A0 (fi

FI78499B (fi

FI853708L (fi

Inventor

Helmut Theunissen

Raymund Weber

Original Assignee

Hydrocor Forsch Analytik

Priority date (The priority date 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 date listed.)

1984-01-27

Filing date

1985-09-26

Publication date

1989-08-10

1985-09-26 Application filed by Hydrocor Forsch Analytik filed Critical Hydrocor Forsch Analytik

1985-09-26 Publication of FI853708A0 publication Critical patent/FI853708A0/fi

1985-09-26 Publication of FI853708L publication Critical patent/FI853708L/fi

1989-04-28 Application granted granted Critical

1989-04-28 Publication of FI78499B publication Critical patent/FI78499B/fi

1989-08-10 Publication of FI78499C publication Critical patent/FI78499C/fi

Links

239000012530 fluid Substances 0.000 title claims description 45
239000007788 liquid Substances 0.000 claims abstract description 32
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 14
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 14
229910052794 bromium Inorganic materials 0.000 claims abstract description 14
QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical class C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 claims description 33
QQSRMERJTBKKCV-UHFFFAOYSA-N (1,1-dibromo-2-phenylethyl)benzene Chemical compound C=1C=CC=CC=1C(Br)(Br)CC1=CC=CC=C1 QQSRMERJTBKKCV-UHFFFAOYSA-N 0.000 claims description 20
238000005260 corrosion Methods 0.000 claims description 14
230000007797 corrosion Effects 0.000 claims description 13
239000003112 inhibitor Substances 0.000 claims description 10
239000000654 additive Substances 0.000 claims description 7
239000003795 chemical substances by application Substances 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 5
239000000126 substance Substances 0.000 claims description 4
FTRWFZZSIXRXFI-UHFFFAOYSA-N 1-bromo-4-(2-phenylethyl)benzene Chemical compound C1=CC(Br)=CC=C1CCC1=CC=CC=C1 FTRWFZZSIXRXFI-UHFFFAOYSA-N 0.000 claims 1
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims 1
229910052804 chromium Inorganic materials 0.000 claims 1
239000011651 chromium Substances 0.000 claims 1
238000010616 electrical installation Methods 0.000 claims 1
-1 benzyl toluol derivative Chemical class 0.000 abstract description 4
150000001875 compounds Chemical class 0.000 description 17
239000000203 mixture Substances 0.000 description 16
238000012360 testing method Methods 0.000 description 11
231100000331 toxic Toxicity 0.000 description 9
230000002588 toxic effect Effects 0.000 description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 8
239000000047 product Substances 0.000 description 7
YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 7
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 6
150000001412 amines Chemical class 0.000 description 5
230000000694 effects Effects 0.000 description 5
MEIUXJOXEUYBRW-UHFFFAOYSA-N 1,2-dichloro-3-(1,1-dichloro-2-phenylethyl)benzene Chemical compound ClC1=CC=CC(C(Cl)(Cl)CC=2C=CC=CC=2)=C1Cl MEIUXJOXEUYBRW-UHFFFAOYSA-N 0.000 description 4
238000011835 investigation Methods 0.000 description 4
YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 description 4
150000003071 polychlorinated biphenyls Chemical class 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000007787 solid Substances 0.000 description 4
239000000725 suspension Substances 0.000 description 4
239000003760 tallow Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
QSSXJPIWXQTSIX-UHFFFAOYSA-N 1-bromo-2-methylbenzene Chemical compound CC1=CC=CC=C1Br QSSXJPIWXQTSIX-UHFFFAOYSA-N 0.000 description 3
RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
229920002367 Polyisobutene Polymers 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
230000031709 bromination Effects 0.000 description 3
238000005893 bromination reaction Methods 0.000 description 3
125000001246 bromo group Chemical group Br* 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
238000000354 decomposition reaction Methods 0.000 description 3
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 3
239000003822 epoxy resin Substances 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
230000002349 favourable effect Effects 0.000 description 3
239000003063 flame retardant Substances 0.000 description 3
230000002209 hydrophobic effect Effects 0.000 description 3
230000001050 lubricating effect Effects 0.000 description 3
229920000647 polyepoxide Polymers 0.000 description 3
239000003381 stabilizer Substances 0.000 description 3
229910052725 zinc Inorganic materials 0.000 description 3
239000011701 zinc Substances 0.000 description 3
HGUFODBRKLSHSI-UHFFFAOYSA-N 2,3,7,8-tetrachloro-dibenzo-p-dioxin Chemical compound O1C2=CC(Cl)=C(Cl)C=C2OC2=C1C=C(Cl)C(Cl)=C2 HGUFODBRKLSHSI-UHFFFAOYSA-N 0.000 description 2
229920002449 FKM Polymers 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
150000001491 aromatic compounds Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
238000009835 boiling Methods 0.000 description 2
229910052793 cadmium Inorganic materials 0.000 description 2
239000003990 capacitor Substances 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
238000006482 condensation reaction Methods 0.000 description 2
TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 description 2
150000002013 dioxins Chemical class 0.000 description 2
CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical class C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 2
150000002334 glycols Chemical class 0.000 description 2
150000002367 halogens Chemical group 0.000 description 2
230000009931 harmful effect Effects 0.000 description 2
229910000042 hydrogen bromide Inorganic materials 0.000 description 2
238000001819 mass spectrum Methods 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
238000000034 method Methods 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
229920000193 polymethacrylate Polymers 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
239000000565 sealant Substances 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
238000010998 test method Methods 0.000 description 2
QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
GDPISEKNRFFKMM-UHFFFAOYSA-N 1,3-diphenylpropan-2-ylbenzene Chemical class C=1C=CC=CC=1CC(C=1C=CC=CC=1)CC1=CC=CC=C1 GDPISEKNRFFKMM-UHFFFAOYSA-N 0.000 description 1
PQTAUFTUHHRKSS-UHFFFAOYSA-N 1-benzyl-2-methylbenzene Chemical class CC1=CC=CC=C1CC1=CC=CC=C1 PQTAUFTUHHRKSS-UHFFFAOYSA-N 0.000 description 1
NVLHGZIXTRYOKT-UHFFFAOYSA-N 1-chloro-2,3-dimethylbenzene Chemical group CC1=CC=CC(Cl)=C1C NVLHGZIXTRYOKT-UHFFFAOYSA-N 0.000 description 1
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
229910001369 Brass Inorganic materials 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
238000005727 Friedel-Crafts reaction Methods 0.000 description 1
229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
FJMNNXLGOUYVHO-UHFFFAOYSA-N aluminum zinc Chemical compound [Al].[Zn] FJMNNXLGOUYVHO-UHFFFAOYSA-N 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
150000004056 anthraquinones Chemical class 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
229910052788 barium Inorganic materials 0.000 description 1
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
DALDUXIBIKGWTK-UHFFFAOYSA-N benzene;toluene Chemical class C1=CC=CC=C1.CC1=CC=CC=C1 DALDUXIBIKGWTK-UHFFFAOYSA-N 0.000 description 1
KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
238000006065 biodegradation reaction Methods 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
150000001616 biphenylenes Chemical class 0.000 description 1
239000010951 brass Substances 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000005660 chlorination reaction Methods 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
238000005352 clarification Methods 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000010276 construction Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
TVZPLCNGKSPOJA-UHFFFAOYSA-N copper zinc Chemical compound [Cu].[Zn] TVZPLCNGKSPOJA-UHFFFAOYSA-N 0.000 description 1
239000007857 degradation product Substances 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
238000001514 detection method Methods 0.000 description 1
150000004826 dibenzofurans Chemical class 0.000 description 1
VCJZTATVUDMNLU-UHFFFAOYSA-N dibromomethylbenzene Chemical compound BrC(Br)C1=CC=CC=C1 VCJZTATVUDMNLU-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
125000006840 diphenylmethane group Chemical group 0.000 description 1
230000005684 electric field Effects 0.000 description 1
238000004710 electron pair approximation Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
230000007613 environmental effect Effects 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
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
238000007710 freezing Methods 0.000 description 1
230000008014 freezing Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
230000002140 halogenating effect Effects 0.000 description 1
230000026030 halogenation Effects 0.000 description 1
238000005658 halogenation reaction Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000003999 initiator Substances 0.000 description 1
239000002054 inoculum Substances 0.000 description 1
238000009413 insulation Methods 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
230000001678 irradiating effect Effects 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
239000010687 lubricating oil Substances 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
230000002906 microbiologic effect Effects 0.000 description 1
244000005700 microbiome Species 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
238000012545 processing Methods 0.000 description 1
238000000197 pyrolysis Methods 0.000 description 1
239000002516 radical scavenger Substances 0.000 description 1
238000011160 research Methods 0.000 description 1
230000002441 reversible effect Effects 0.000 description 1
238000012216 screening Methods 0.000 description 1
239000003566 sealing material Substances 0.000 description 1
230000028327 secretion Effects 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
230000002269 spontaneous effect Effects 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
239000012085 test solution Substances 0.000 description 1
CRHIAMBJMSSNNM-UHFFFAOYSA-N tetraphenylstannane Chemical compound C1=CC=CC=C1[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 CRHIAMBJMSSNNM-UHFFFAOYSA-N 0.000 description 1
150000003613 toluenes Chemical class 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 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
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/50—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing halogen
- C10M105/52—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing halogen containing carbon, hydrogen and halogen only
- 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
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/026—Butene
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/084—Acrylate; Methacrylate
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/02—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
- C10M2211/024—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aromatic
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/06—Perfluorinated compounds
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
- C10M2215/082—Amides [having hydrocarbon substituents containing less than thirty carbon atoms] containing hydroxyl groups; Alkoxylated derivatives
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/26—Amines
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/28—Amides; Imides
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/041—Triaryl phosphates
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/14—Electric or magnetic purposes
- C10N2040/16—Dielectric; Insulating oil or insulators
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/14—Electric or magnetic purposes
- C10N2040/17—Electric or magnetic purposes for electric contacts

Landscapes

Chemical & Material Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Physics & Mathematics (AREA)
Spectroscopy & Molecular Physics (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Biological Depolymerization Polymers (AREA)
Fireproofing Substances (AREA)
Materials For Medical Uses (AREA)
Organic Insulating Materials (AREA)
Purses, Travelling Bags, Baskets, Or Suitcases (AREA)
Measurement And Recording Of Electrical Phenomena And Electrical Characteristics Of The Living Body (AREA)
Chemical And Physical Treatments For Wood And The Like (AREA)
Lubricants (AREA)

FI853708A 1984-01-27 1985-09-26 Svaorantaendlig, biologiskt soenderfallande funktionell vaetska. FI78499C (fi)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
DE19843402863 DE3402863A1 (de)	1984-01-27	1984-01-27	Bromhaltige benzyltoluol-derivate, verfahren zu ihrer herstellung und deren verwendung
DE3402863		1984-01-27
DE8500020		1985-01-25
PCT/DE1985/000020 WO1985003306A1 (fr)	1984-01-27	1985-01-25	Liquide fonctionnel biologiquement degradable et difficilement enflammable

Publications (4)

Publication Number	Publication Date
FI853708A0 FI853708A0 (fi)	1985-09-26
FI853708L FI853708L (fi)	1985-09-26
FI78499B FI78499B (fi)	1989-04-28
FI78499C true FI78499C (fi)	1989-08-10

Family

ID=6226101

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FI853708A FI78499C (fi)	1984-01-27	1985-09-26	Svaorantaendlig, biologiskt soenderfallande funktionell vaetska.

Country Status (11)

Country	Link
EP (1)	EP0150826B1 (de)
JP (1)	JPS61501035A (de)
AT (1)	ATE43628T1 (de)
AU (1)	AU573782B2 (de)
CA (1)	CA1244054A (de)
DE (2)	DE3402863A1 (de)
DK (1)	DK418785A (de)
FI (1)	FI78499C (de)
HU (1)	HU194300B (de)
WO (1)	WO1985003306A1 (de)
ZA (1)	ZA85638B (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3526873A1 (de) *	1985-07-26	1987-01-29	Hydrocor Forsch Analytik	Bromierte alkylbenzolderivate als basis schwerentflammbarer, biologisch abbaubarer funktioneller fluessigkeiten
CN109022034B (zh) *	2018-05-31	2021-02-23	石家庄东翔化工有限公司	用于聚氨酯泡沫填缝剂的阻燃石蜡制备方法
CN114507555B (zh) *	2020-10-28	2023-08-08	中国石油化工股份有限公司	一种可生物降解难燃液压油组合物

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB669048A (en) *	1948-11-19	1952-03-26	Alfred John Rudge	Improvements in or relating to lubricants
US3290253A (en) *	1963-10-21	1966-12-06	Monsanto Res Corp	Chlorine-substituted diarylalkanes as hydraulic fluids
US3371120A (en) *	1964-09-21	1968-02-27	Monsanto Co	3, 4'-halogen-containing diphenyl ethers and thio ethers
DE2336289A1 (de) *	1973-07-17	1975-02-06	Basf Ag	Verfahren zur herstellung von o-benzyltoluolen
FR2273351A1 (de) *	1974-05-31	1975-12-26	Rhone Poulenc Ind
NL7605659A (nl) *	1975-05-30	1976-12-02	Monsanto Co	Elektrisch apparaat.
US4260506A (en) *	1979-01-26	1981-04-07	Monsanto Company	Hydraulic pressure device utilizing biodegradable halogenated diphenyl methanes
GB2100740B (en) *	1981-06-19	1985-03-06	James Edward Stangroom	Electric field responsive (electroviscous) fluids
US4502973A (en) *	1981-06-19	1985-03-05	National Research Development Corporation	Electroviscous fluids
FR2522334B1 (fr) *	1982-02-26	1986-01-10	Ugine Kuhlmann	Application a la lubrification des polychlorobenzyl polychlorotoluenes

1984
- 1984-01-27 DE DE19843402863 patent/DE3402863A1/de not_active Withdrawn
1985
- 1985-01-25 AT AT85100772T patent/ATE43628T1/de not_active IP Right Cessation
- 1985-01-25 WO PCT/DE1985/000020 patent/WO1985003306A1/de not_active Ceased
- 1985-01-25 DE DE8585100772T patent/DE3570692D1/de not_active Expired
- 1985-01-25 AU AU39308/85A patent/AU573782B2/en not_active Ceased
- 1985-01-25 HU HU851051A patent/HU194300B/hu not_active IP Right Cessation
- 1985-01-25 JP JP60500653A patent/JPS61501035A/ja active Pending
- 1985-01-25 EP EP85100772A patent/EP0150826B1/de not_active Expired
- 1985-01-28 ZA ZA85638A patent/ZA85638B/xx unknown
- 1985-01-28 CA CA000472977A patent/CA1244054A/en not_active Expired
- 1985-09-16 DK DK418785A patent/DK418785A/da not_active Application Discontinuation
- 1985-09-26 FI FI853708A patent/FI78499C/fi not_active IP Right Cessation

Also Published As

Publication number	Publication date
JPS61501035A (ja)	1986-05-22
DE3570692D1 (en)	1989-07-06
DK418785D0 (da)	1985-09-16
AU3930885A (en)	1985-08-09
ZA85638B (en)	1985-09-25
DE3402863A1 (de)	1985-08-01
HUT37646A (en)	1986-01-23
ATE43628T1 (de)	1989-06-15
EP0150826A3 (en)	1985-11-06
EP0150826B1 (de)	1989-05-31
FI853708A0 (fi)	1985-09-26
EP0150826A2 (de)	1985-08-07
HU194300B (en)	1988-01-28
CA1244054A (en)	1988-11-01
FI78499B (fi)	1989-04-28
WO1985003306A1 (fr)	1985-08-01
AU573782B2 (en)	1988-06-23
FI853708L (fi)	1985-09-26
DK418785A (da)	1985-09-16

Legal Events

Date	Code	Title	Description
1993-01-25	MM	Patent lapsed
2004-08-31	MM	Patent lapsed	Owner name: HYDROCOR FORSCHUNGS- UND ANALYTIK GMBH

Publication	Publication Date	Title
Erickson et al.	2011	Applications of polychlorinated biphenyls
US4431557A (en)	1984-02-14	Refrigerator oil composition(s)
EP0071338B1 (de)	1985-08-21	Electroviscose Fluids
MXPA06011978A (es)	2007-01-25	Composiciones estabilizadas de trifluoroyodometano.
Broadhurst	1972	Use and replaceability of polychlorinated biphenyls
FI78499C (fi)	1989-08-10	Svaorantaendlig, biologiskt soenderfallande funktionell vaetska.
DE1906293B2 (de)	1978-10-19	Hydraulische Flüssigkeit für Flugzeuge
US2528348A (en)	1950-10-31	Nonflammable hydraulic fluid
JP2700155B2 (ja)	1998-01-19	１．１．１．２−テトラフルオルエタン冷媒を使用する冷凍機用潤滑油
US2033612A (en)	1936-03-10	Chlorine derivatives of dibenzyl and process of preparing them
US4260506A (en)	1981-04-07	Hydraulic pressure device utilizing biodegradable halogenated diphenyl methanes
US3872048A (en)	1975-03-18	Hydraulic and lubricating oil composition
US5106522A (en)	1992-04-21	Fluid compositions
US4179389A (en)	1979-12-18	Stabilized hydraulic fluid
DE3789344T2 (de)	1995-04-06	Dielektrische Isolierflüssigkeit, die Perchloräthylen und einen aliphatischen Kohlenwasserstoff enthält.
US3941706A (en)	1976-03-02	Functional liquid
US4179384A (en)	1979-12-18	Stabilized hydraulic fluid
US2171855A (en)	1939-09-05	Dielectric composition
US4210542A (en)	1980-07-01	Multicomponent stabilized hydraulic fluid
CA1081937A (en)	1980-07-22	Electrical devices containing readily biodegradable dielectric fluids
Metcalfe et al.	1988	Polychlorinated biphenyls (PCBs) physical and chemical property data
US2169995A (en)	1939-08-22	Liquid dielectric compositions
CA1075889A (en)	1980-04-22	Dielectric fluid
US3432436A (en)	1969-03-11	Halogenated fluids
EP0204196A1 (de)	1986-12-10	Bromierte Alkylbenzole als Basis schwerentflammbarer, biologisch abbaubarer funktioneller Flüssigkeiten