HU194300B - Heat-resistante biologically decomposing oricessubg liquid - Google Patents

Heat-resistante biologically decomposing oricessubg liquid Download PDF

Info

Publication number: HU194300B
Authority: HU; Hungary
Prior art keywords: working fluid; derivatives; liquid; refractory; dibromomethyldiphenylmethane
Prior art date: 1984-01-27

Application number

HU851051A

Other languages

English (en)

Hungarian (hu)

Other versions

HUT37646A (en

Inventor

Helmut Theunissen

Raymund Weber

Original Assignee

Hydrocor Forsch Analytik Gmbh

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

1985-01-25

Publication date

1988-01-28

1985-01-25 Application filed by Hydrocor Forsch Analytik Gmbh filed Critical Hydrocor Forsch Analytik Gmbh

1986-01-23 Publication of HUT37646A publication Critical patent/HUT37646A/hu

1988-01-28 Publication of HU194300B publication Critical patent/HU194300B/hu

Links

239000007788 liquid Substances 0.000 title abstract description 12
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 9
229910052794 bromium Inorganic materials 0.000 claims abstract description 9
239000012530 fluid Substances 0.000 claims description 47
CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical class C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 claims description 19
BLAWIKIQYUONHM-UHFFFAOYSA-N (2,2-dibromo-1-phenylethyl)benzene Chemical compound C=1C=CC=CC=1C(C(Br)Br)C1=CC=CC=C1 BLAWIKIQYUONHM-UHFFFAOYSA-N 0.000 claims description 17
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 6
239000000654 additive Substances 0.000 claims description 6
229910052725 zinc Inorganic materials 0.000 claims description 6
239000011701 zinc Substances 0.000 claims description 6
150000001412 amines Chemical class 0.000 claims description 5
125000001246 bromo group Chemical group Br* 0.000 claims description 5
239000003795 chemical substances by application Substances 0.000 claims description 5
229910052788 barium Inorganic materials 0.000 claims description 3
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 3
230000007797 corrosion Effects 0.000 claims description 3
238000005260 corrosion Methods 0.000 claims description 3
235000014113 dietary fatty acids Nutrition 0.000 claims description 3
239000000194 fatty acid Substances 0.000 claims description 3
229930195729 fatty acid Natural products 0.000 claims description 3
150000004665 fatty acids Chemical class 0.000 claims description 3
230000003647 oxidation Effects 0.000 claims description 3
238000007254 oxidation reaction Methods 0.000 claims description 3
239000003381 stabilizer Substances 0.000 claims description 3
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 3
239000002253 acid Substances 0.000 claims description 2
239000003623 enhancer Substances 0.000 claims description 2
239000003822 epoxy resin Substances 0.000 claims description 2
239000003112 inhibitor Substances 0.000 claims description 2
229920000647 polyepoxide Polymers 0.000 claims description 2
SLHSRCBFPHCSGL-UHFFFAOYSA-N (3-bromo-1-phenylpropyl)benzene Chemical compound C=1C=CC=CC=1C(CCBr)C1=CC=CC=C1 SLHSRCBFPHCSGL-UHFFFAOYSA-N 0.000 claims 1
IWPTVBMXQDKDBP-UHFFFAOYSA-N 1-benzyl-2,3,4-trimethylbenzene Chemical compound CC1=C(C)C(C)=CC=C1CC1=CC=CC=C1 IWPTVBMXQDKDBP-UHFFFAOYSA-N 0.000 claims 1
-1 benzyl toluol derivative Chemical class 0.000 abstract description 9
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract description 8
150000001875 compounds Chemical class 0.000 description 15
239000000047 product Substances 0.000 description 10
238000012360 testing method Methods 0.000 description 8
231100000331 toxic Toxicity 0.000 description 7
230000002588 toxic effect Effects 0.000 description 7
QSSXJPIWXQTSIX-UHFFFAOYSA-N 1-bromo-2-methylbenzene Chemical compound CC1=CC=CC=C1Br QSSXJPIWXQTSIX-UHFFFAOYSA-N 0.000 description 6
238000000034 method Methods 0.000 description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
238000007789 sealing Methods 0.000 description 6
230000008859 change Effects 0.000 description 5
230000008901 benefit Effects 0.000 description 4
239000000460 chlorine Substances 0.000 description 4
TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 description 4
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
239000000203 mixture Substances 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
238000005457 optimization Methods 0.000 description 4
238000002360 preparation method Methods 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
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 3
YXALYBMHAYZKAP-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptan-4-ylmethyl 7-oxabicyclo[4.1.0]heptane-4-carboxylate Chemical compound C1CC2OC2CC1C(=O)OCC1CC2OC2CC1 YXALYBMHAYZKAP-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
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
230000000996 additive effect Effects 0.000 description 3
229940054021 anxiolytics diphenylmethane derivative Drugs 0.000 description 3
229910052793 cadmium Inorganic materials 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
238000002485 combustion reaction Methods 0.000 description 3
238000006482 condensation reaction Methods 0.000 description 3
239000000470 constituent Substances 0.000 description 3
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical class C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 3
230000000694 effects Effects 0.000 description 3
230000002349 favourable effect Effects 0.000 description 3
150000002367 halogens Chemical group 0.000 description 3
230000002209 hydrophobic effect Effects 0.000 description 3
231100000053 low toxicity Toxicity 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
238000005070 sampling Methods 0.000 description 3
RWWBIXFAJZCCQX-UHFFFAOYSA-N (2-bromo-1-phenylethyl)benzene Chemical compound C=1C=CC=CC=1C(CBr)C1=CC=CC=C1 RWWBIXFAJZCCQX-UHFFFAOYSA-N 0.000 description 2
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 2
QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical class C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
229920002449 FKM Polymers 0.000 description 2
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
125000006267 biphenyl group Chemical group 0.000 description 2
BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 2
239000003990 capacitor Substances 0.000 description 2
230000015556 catabolic process Effects 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
238000000354 decomposition reaction Methods 0.000 description 2
238000006731 degradation reaction Methods 0.000 description 2
239000003989 dielectric material Substances 0.000 description 2
230000007613 environmental effect Effects 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000001819 mass spectrum Methods 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
150000003071 polychlorinated biphenyls Chemical class 0.000 description 2
239000000565 sealant Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000007858 starting material Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
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 description 1
YKHLXWRASLDFOZ-UHFFFAOYSA-N (2-bromo-1,3-diphenylpropan-2-yl)benzene Chemical compound C=1C=CC=CC=1CC(C=1C=CC=CC=1)(Br)CC1=CC=CC=C1 YKHLXWRASLDFOZ-UHFFFAOYSA-N 0.000 description 1
GBDZXPJXOMHESU-UHFFFAOYSA-N 1,2,3,4-tetrachlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1Cl GBDZXPJXOMHESU-UHFFFAOYSA-N 0.000 description 1
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
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 1
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-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
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
208000033962 Fontaine progeroid syndrome Diseases 0.000 description 1
238000005727 Friedel-Crafts reaction Methods 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 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
HNBFCAMUUALGHT-UHFFFAOYSA-N [dibromo(phenyl)methyl]benzene Chemical class C=1C=CC=CC=1C(Br)(Br)C1=CC=CC=C1 HNBFCAMUUALGHT-UHFFFAOYSA-N 0.000 description 1
230000009471 action Effects 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
229910052782 aluminium Inorganic materials 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
125000000129 anionic group Chemical group 0.000 description 1
239000007866 anti-wear additive Substances 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
125000005605 benzo group Chemical group 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
238000009835 boiling Methods 0.000 description 1
239000010951 brass Substances 0.000 description 1
230000031709 bromination Effects 0.000 description 1
238000005893 bromination reaction Methods 0.000 description 1
KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000003153 chemical reaction reagent Substances 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
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
230000008878 coupling Effects 0.000 description 1
238000010168 coupling process Methods 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
239000007857 degradation product Substances 0.000 description 1
238000001514 detection method Methods 0.000 description 1
VCJZTATVUDMNLU-UHFFFAOYSA-N dibromomethylbenzene Chemical compound BrC(Br)C1=CC=CC=C1 VCJZTATVUDMNLU-UHFFFAOYSA-N 0.000 description 1
150000002013 dioxins Chemical class 0.000 description 1
125000006840 diphenylmethane group Chemical group 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
230000005684 electric field Effects 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
238000003912 environmental pollution Methods 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
231100001261 hazardous Toxicity 0.000 description 1
230000036541 health Effects 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000011534 incubation Methods 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
239000000314 lubricant Substances 0.000 description 1
230000007257 malfunction Effects 0.000 description 1
238000004949 mass spectrometry Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
238000005259 measurement Methods 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
235000010446 mineral oil Nutrition 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
238000013021 overheating Methods 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
230000008569 process Effects 0.000 description 1
238000000197 pyrolysis Methods 0.000 description 1
239000011541 reaction mixture Substances 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
238000009987 spinning Methods 0.000 description 1
239000010959 steel Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
238000010998 test method Methods 0.000 description 1
CRHIAMBJMSSNNM-UHFFFAOYSA-N tetraphenylstannane Chemical group 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
230000002110 toxicologic effect Effects 0.000 description 1
231100000027 toxicology Toxicity 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
239000008096 xylene Substances 0.000 description 1
235000013618 yogurt Nutrition 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)

HU851051A 1984-01-27 1985-01-25 Heat-resistante biologically decomposing oricessubg liquid HU194300B (en)

Applications Claiming Priority (1)

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

Publications (2)

Publication Number	Publication Date
HUT37646A HUT37646A (en)	1986-01-23
HU194300B true HU194300B (en)	1988-01-28

Family

ID=6226101

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
HU851051A HU194300B (en)	1984-01-27	1985-01-25	Heat-resistante biologically decomposing oricessubg liquid

Country Status (11)

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

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 (da) *	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
FI78499C (fi)	1989-08-10
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
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
1990-06-28	HU90	Patent valid on 900628
1994-09-28	HMM4	Cancellation of final prot. due to non-payment of fee

Publication	Publication Date	Title
US4431557A (en)	1984-02-14	Refrigerator oil composition(s)
Erickson et al.	2011	Applications of polychlorinated biphenyls
US7294608B2 (en)	2007-11-13	Use of calcium sulfonate based threaded compounds in drilling operations and other severe industrial applications
KR20040020908A (ko)	2004-03-09	고온 윤활제 조성물
EP0475141B1 (en)	1994-02-23	Additive for lubricating oil and lubricating oil composition containing said additive
HU194300B (en)	1988-01-28	Heat-resistante biologically decomposing oricessubg liquid
CN1100130C (zh)	2003-01-29	一种用于电触点的润滑脂
CA2632500A1 (en)	2007-06-14	A composition of hydraulic fluid and process for the preparation thereof
US2528348A (en)	1950-10-31	Nonflammable hydraulic fluid
JPH02102296A (ja)	1990-04-13	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
US2249626A (en)	1941-07-15	Lubricating composition
JP2005511815A (ja)	2005-04-28	三種の基油の混合物およびそれに基づく潤滑油組成物
US5370808A (en)	1994-12-06	Filling grease composition for automobile wire harness connector
US4179389A (en)	1979-12-18	Stabilized hydraulic fluid
US5300245A (en)	1994-04-05	Working fluid composition having ketone-containing compound for use in refrigeration system
US4497721A (en)	1985-02-05	Refrigerator oil composition
US3941706A (en)	1976-03-02	Functional liquid
US4179384A (en)	1979-12-18	Stabilized hydraulic fluid
US3305487A (en)	1967-02-21	Hydraulic fluids
US2171855A (en)	1939-09-05	Dielectric composition
US5308907A (en)	1994-05-03	Low smoke power cable sealant
CN100430368C (zh)	2008-11-05	生产烷基化二苯胺的方法
US2195510A (en)	1940-04-02	Lubricant containing di-iso-butyl phenol
US4596664A (en)	1986-06-24	Non-flammable hydraulic fluids
US4305833A (en)	1981-12-15	Lubricating oils containing acetoacetanilides as antioxidants