DE60117243T2 - Wärmeübertragungsflüssigkeit basierend auf polyphenylmethanen mit verbesserter thermischer stabilität - Google Patents
Wärmeübertragungsflüssigkeit basierend auf polyphenylmethanen mit verbesserter thermischer stabilität Download PDFInfo
- Publication number
- DE60117243T2 DE60117243T2 DE60117243T DE60117243T DE60117243T2 DE 60117243 T2 DE60117243 T2 DE 60117243T2 DE 60117243 T DE60117243 T DE 60117243T DE 60117243 T DE60117243 T DE 60117243T DE 60117243 T2 DE60117243 T2 DE 60117243T2
- Authority
- DE
- Germany
- Prior art keywords
- mixture
- formula
- compounds
- heat transfer
- products
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000013529 heat transfer fluid Substances 0.000 title claims abstract description 22
- 239000000203 mixture Substances 0.000 claims abstract description 131
- 150000001875 compounds Chemical class 0.000 claims description 38
- 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 claims description 27
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 15
- 229920000265 Polyparaphenylene Polymers 0.000 claims description 6
- -1 polyphenylene Polymers 0.000 claims description 6
- 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 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 238000012986 modification Methods 0.000 claims description 4
- 230000004048 modification Effects 0.000 claims description 4
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical class C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims 1
- LIJPUYWRAJPDLJ-UHFFFAOYSA-N 1-benzyl-1,2,3,4-tetrahydronaphthalene Chemical compound C1CCC2=CC=CC=C2C1CC1=CC=CC=C1 LIJPUYWRAJPDLJ-UHFFFAOYSA-N 0.000 abstract description 4
- 229920006389 polyphenyl polymer Polymers 0.000 abstract description 3
- 239000000047 product Substances 0.000 description 50
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 29
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 27
- 238000012546 transfer Methods 0.000 description 21
- 239000012530 fluid Substances 0.000 description 20
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
- 238000004821 distillation Methods 0.000 description 16
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 10
- 229910052757 nitrogen Inorganic materials 0.000 description 9
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 8
- 229940073608 benzyl chloride Drugs 0.000 description 8
- 238000002474 experimental method Methods 0.000 description 8
- 239000008096 xylene Substances 0.000 description 8
- 238000009835 boiling Methods 0.000 description 7
- 239000007789 gas Substances 0.000 description 7
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- MTZFOCOZXPUVIC-UHFFFAOYSA-N 5-benzyl-1,2,3,4-tetrahydronaphthalene Chemical compound C=1C=CC=2CCCCC=2C=1CC1=CC=CC=C1 MTZFOCOZXPUVIC-UHFFFAOYSA-N 0.000 description 5
- HUWLTXHUXZFUHP-UHFFFAOYSA-N 6-benzyl-1,2,3,4-tetrahydronaphthalene Chemical compound C=1C=C2CCCCC2=CC=1CC1=CC=CC=C1 HUWLTXHUXZFUHP-UHFFFAOYSA-N 0.000 description 5
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000010835 comparative analysis Methods 0.000 description 4
- 229910001502 inorganic halide Inorganic materials 0.000 description 4
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 0 *N1C=CC=CC1 Chemical compound *N1C=CC=CC1 0.000 description 3
- ATZAQOQMJXMCHK-UHFFFAOYSA-N 6-(1-phenylethyl)-1,2,3,4-tetrahydronaphthalene Chemical compound C=1C=C2CCCCC2=CC=1C(C)C1=CC=CC=C1 ATZAQOQMJXMCHK-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 238000010926 purge Methods 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 238000001577 simple distillation Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- OGVRJXPGSVLDRD-UHFFFAOYSA-N 2,3-dimethylanthracene Chemical compound C1=CC=C2C=C(C=C(C(C)=C3)C)C3=CC2=C1 OGVRJXPGSVLDRD-UHFFFAOYSA-N 0.000 description 2
- TXOHWLOHKUPUKO-UHFFFAOYSA-N 5-(1-phenylethyl)-1,2,3,4-tetrahydronaphthalene Chemical compound C=1C=CC=2CCCCC=2C=1C(C)C1=CC=CC=C1 TXOHWLOHKUPUKO-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 2
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 230000001174 ascending effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 238000004508 fractional distillation Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000006178 methyl benzyl group Chemical group 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 150000001911 terphenyls Chemical class 0.000 description 2
- 150000003738 xylenes Chemical class 0.000 description 2
- MHCVCKDNQYMGEX-UHFFFAOYSA-N 1,1'-biphenyl;phenoxybenzene Chemical compound C1=CC=CC=C1C1=CC=CC=C1.C=1C=CC=CC=1OC1=CC=CC=C1 MHCVCKDNQYMGEX-UHFFFAOYSA-N 0.000 description 1
- PKQYSCBUFZOAPE-UHFFFAOYSA-N 1,2-dibenzyl-3-methylbenzene Chemical class C=1C=CC=CC=1CC=1C(C)=CC=CC=1CC1=CC=CC=C1 PKQYSCBUFZOAPE-UHFFFAOYSA-N 0.000 description 1
- GTLWADFFABIGAE-UHFFFAOYSA-N 1-chloroethylbenzene Chemical compound CC(Cl)C1=CC=CC=C1 GTLWADFFABIGAE-UHFFFAOYSA-N 0.000 description 1
- WJPCNSUAYRKXLS-UHFFFAOYSA-N 3,4,4-tribenzyl-2,3-dihydro-1h-naphthalene Chemical class C=1C=CC=CC=1CC1CCC2=CC=CC=C2C1(CC=1C=CC=CC=1)CC1=CC=CC=C1 WJPCNSUAYRKXLS-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- DAMJCWMGELCIMI-UHFFFAOYSA-N benzyl n-(2-oxopyrrolidin-3-yl)carbamate Chemical compound C=1C=CC=CC=1COC(=O)NC1CCNC1=O DAMJCWMGELCIMI-UHFFFAOYSA-N 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- ZCILODAAHLISPY-UHFFFAOYSA-N biphenyl ether Natural products C1=C(CC=C)C(O)=CC(OC=2C(=CC(CC=C)=CC=2)O)=C1 ZCILODAAHLISPY-UHFFFAOYSA-N 0.000 description 1
- 150000004074 biphenyls Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical compound C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 description 1
- 238000006298 dechlorination reaction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000006836 terphenylene group Chemical group 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/08—Materials not undergoing a change of physical state when used
- C09K5/10—Liquid materials
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Combustion & Propulsion (AREA)
- Thermal Sciences (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Lubricants (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0003944 | 2000-03-29 | ||
| FR0003944A FR2807059B1 (fr) | 2000-03-29 | 2000-03-29 | Fluide de transfert de chaleur a base de polyphenylmethanes ayant une stabilite thermique amelioree |
| PCT/FR2001/000930 WO2001072924A1 (fr) | 2000-03-29 | 2001-03-27 | Fluide de transfert de chaleur a base de polyphenylmethanes ayant une stabilite thermique amelioree |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60117243D1 DE60117243D1 (de) | 2006-04-20 |
| DE60117243T2 true DE60117243T2 (de) | 2007-02-15 |
Family
ID=8848596
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60117243T Expired - Lifetime DE60117243T2 (de) | 2000-03-29 | 2001-03-27 | Wärmeübertragungsflüssigkeit basierend auf polyphenylmethanen mit verbesserter thermischer stabilität |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US7011765B2 (enExample) |
| EP (1) | EP1268705B1 (enExample) |
| JP (1) | JP4845319B2 (enExample) |
| CN (1) | CN1200989C (enExample) |
| AT (1) | ATE317885T1 (enExample) |
| AU (1) | AU2001246654A1 (enExample) |
| DE (1) | DE60117243T2 (enExample) |
| ES (1) | ES2258522T3 (enExample) |
| FR (1) | FR2807059B1 (enExample) |
| NO (1) | NO20024655L (enExample) |
| WO (1) | WO2001072924A1 (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100584809C (zh) * | 2006-12-18 | 2010-01-27 | 宝山钢铁股份有限公司 | 1，2，3，4-四氢化萘传热流体的再生利用工艺 |
| US9010318B2 (en) | 2009-09-04 | 2015-04-21 | Wisconsin Alumni Research Foundation | Extended-range heat transfer fluid using variable composition |
| CN104178092A (zh) * | 2013-05-27 | 2014-12-03 | 山东恒导石油化工股份有限公司 | 一种高温有机热载体及其生产工艺 |
| CN106349000B (zh) * | 2015-07-17 | 2018-10-26 | 江苏中能化学科技股份有限公司 | 导热流体1-苯基-1-(环己基甲苯)基乙烷异构体及其合成方法 |
| US10584271B2 (en) * | 2016-12-20 | 2020-03-10 | ORG Chem Group | Heat transfer fluid and process for preparing same |
| FR3077295A1 (fr) | 2018-01-31 | 2019-08-02 | Arkema France | Utilisation d'un compose polyaryle comme fluide de transfert de chaleur |
| FR3106345B1 (fr) * | 2020-01-20 | 2023-07-21 | Arkema France | Utilisation d’une composition de transfert de chaleur pour réguler la température d’une batterie |
| FR3117113B1 (fr) * | 2020-12-09 | 2024-04-12 | Arkema France | Formulation liquide pour stockage d’hydrogène |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5654353B2 (enExample) * | 1973-02-12 | 1981-12-24 | ||
| JPS6169736A (ja) * | 1984-09-14 | 1986-04-10 | Idemitsu Kosan Co Ltd | テトラリン誘導体の製法 |
| JPS62246997A (ja) * | 1986-04-21 | 1987-10-28 | Idemitsu Kosan Co Ltd | トラクシヨンドライブ用流体 |
| JPS62263133A (ja) * | 1986-05-12 | 1987-11-16 | Idemitsu Kosan Co Ltd | ジアラルキル芳香族炭化水素の製造方法 |
| GB8615400D0 (en) * | 1986-06-24 | 1986-07-30 | Isc Chemicals Ltd | Flourinated polycyclic compounds |
| FR2618142B1 (fr) * | 1987-07-16 | 1989-10-06 | Atochem | Compositions d'oligomeres de polyarylalcanes contenant des motifs xylene et leur procede de fabrication |
| US4956120A (en) * | 1987-07-16 | 1990-09-11 | Atochem | Polyarylalkane oligomer compositions and process for their manufacture |
| US5192463A (en) | 1989-02-20 | 1993-03-09 | Atochem | Low temperature, polyphenylmethane-based dielectric compositions |
| FR2643366B1 (fr) * | 1989-02-20 | 1991-09-06 | Atochem | Compositions a base de polyphenylmethanes, leur procede de fabrication et leur application comme dielectrique |
| FR2658812B1 (fr) * | 1990-02-27 | 1992-05-15 | Atochem | Compositions dielectriques a base de benzyltoluene et de (methylbenzyl) xylene. |
| JP2760643B2 (ja) * | 1990-08-03 | 1998-06-04 | 東燃株式会社 | ジフェニルブタンの製造方法 |
| FR2673189A1 (fr) * | 1991-02-22 | 1992-08-28 | Atochem | Utilisation d'isomeres de mono et bis(methylbenzyl)xylene comme fluide de transfert technique. |
| DE69804442T2 (de) * | 1997-05-09 | 2002-08-08 | The Dow Chemical Co., Midland | Wärmetransportflüssigkeitsmischungen enthaltend 1,2,3,4-tetrahydro-(1-phenyl)naphthalen |
-
2000
- 2000-03-29 FR FR0003944A patent/FR2807059B1/fr not_active Expired - Fee Related
-
2001
- 2001-03-27 AT AT01919583T patent/ATE317885T1/de not_active IP Right Cessation
- 2001-03-27 JP JP2001571841A patent/JP4845319B2/ja not_active Expired - Fee Related
- 2001-03-27 EP EP01919583A patent/EP1268705B1/fr not_active Expired - Lifetime
- 2001-03-27 AU AU2001246654A patent/AU2001246654A1/en not_active Abandoned
- 2001-03-27 WO PCT/FR2001/000930 patent/WO2001072924A1/fr not_active Ceased
- 2001-03-27 DE DE60117243T patent/DE60117243T2/de not_active Expired - Lifetime
- 2001-03-27 ES ES01919583T patent/ES2258522T3/es not_active Expired - Lifetime
- 2001-03-27 CN CN01810395.2A patent/CN1200989C/zh not_active Expired - Fee Related
- 2001-03-27 US US10/240,093 patent/US7011765B2/en not_active Expired - Lifetime
-
2002
- 2002-09-27 NO NO20024655A patent/NO20024655L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| US7011765B2 (en) | 2006-03-14 |
| FR2807059B1 (fr) | 2002-05-17 |
| NO20024655D0 (no) | 2002-09-27 |
| WO2001072924A1 (fr) | 2001-10-04 |
| EP1268705B1 (fr) | 2006-02-15 |
| CN1200989C (zh) | 2005-05-11 |
| AU2001246654A1 (en) | 2001-10-08 |
| NO20024655L (no) | 2002-11-01 |
| FR2807059A1 (fr) | 2001-10-05 |
| ATE317885T1 (de) | 2006-03-15 |
| JP4845319B2 (ja) | 2011-12-28 |
| CN1432054A (zh) | 2003-07-23 |
| ES2258522T3 (es) | 2006-09-01 |
| US20040031949A1 (en) | 2004-02-19 |
| DE60117243D1 (de) | 2006-04-20 |
| JP2003528970A (ja) | 2003-09-30 |
| EP1268705A1 (fr) | 2003-01-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE60117243T2 (de) | Wärmeübertragungsflüssigkeit basierend auf polyphenylmethanen mit verbesserter thermischer stabilität | |
| DE69222616T2 (de) | Auf Benzyltoluol und Benzylxylol basierende Zusammensetzung | |
| DE60101156T2 (de) | Zusammensetzungen von mono- und polybenzyl-1,2,3,4-tetrahydronaphthalen, verwendung dieser zusammensetzungen oder von einer isomerenmischung von monobenzyl-1,2,3,4-tetrahydronaphthalen als wärmeübertragungsmittel | |
| DE69002964T2 (de) | Auf Polyphenylmethanen basierende Zusammensetzungen, Verfahren zu ihrer Herstellung und ihre Verwendung als Dielektrikum. | |
| DE1902843B2 (enExample) | ||
| DE962793C (de) | Verfahren zur Herstellung von Phenyldichlorsilan | |
| DE2231962B2 (de) | Verfahren zur Herstellung von Speziallösungsmitteln für organische Verbindungen mit funktionellen Gruppen | |
| DE69209868T2 (de) | Verwendung von Isomeren von Mono- und bis(methylbenzyle)xylen als Wärmeübertragungflüssigkeit | |
| DE69212965T2 (de) | Verfahren zur herstellung von arylketonen | |
| DE2429294A1 (de) | Arbeitsfluessigkeit | |
| DE740677C (de) | Verfahren zur Herstellung von hoehermolekularen aliphatischen Chlorkohlenwasserstoffen | |
| CH255096A (de) | Verfahren zum Reinigen von rohem Acrylonitril. | |
| DE1921842A1 (de) | Verfahren zur Herstellung von cycloaliphatischen Halogeniden | |
| DE2558475C3 (de) | Verfahren zur Herstellung eines als synthetisches Schmieröl brauchbaren Oligomeren mit etwa 20 bis 60 Kohlenstoffatomen | |
| DE2411496C2 (de) | Verfahren zur Herstellung von flüssigen Polymeren mit sehr hoher Viskosität | |
| DE2736948C3 (de) | Verfahren zur Herstellung eines aromatischen Monovinylidenmonomeren durch Dehydratisieren | |
| EP0558816B1 (de) | Verfahren zur Herstellung von monobenzylierten Alkylbiphenylen und deren Verwendung | |
| DE2526615A1 (de) | Verfahren zur oligomerisierung von alpha-olefinen und dafuer brauchbares katalysatorsystem | |
| DE1442849A1 (de) | Verfahren zur Durchfuehrung von chemischen Reaktionen | |
| DE2732830C2 (de) | Verfahren zur Herstellung eines m-Isocamphylphenol enthaltenden Produkts durch katalytische Isomerisierung von p-Isocamphylphenol oder eines p-Isocamphylphenol enthaltenden Gemisches | |
| DE2510088C2 (de) | Verfahren zur fraktionierten Destillation von Diacetoxybutenisomeren | |
| DE553149C (de) | Verfahren zur ununterbrochenen Darstellung von Dichloraethylen aus Acetylen und Chlor | |
| AT232990B (de) | Verfahren zur Herstellung von neuen Diperoxyden | |
| DE1468639C (de) | Verfahren zur Herstellung von bei Raumtemperatur flüssigen Gemischen von Äthylterphenylen | |
| DE1905071C3 (de) | Verfahren zur Raffination linearer Alkylbenzole |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition |