NO300979B1 - Anvendelse av mono- og bis(metylbenzyl)xylenisomerer som termisk overföringsfluid - Google Patents

Anvendelse av mono- og bis(metylbenzyl)xylenisomerer som termisk overföringsfluid

Info

Publication number: NO300979B1
Authority: NO; Norway
Prior art keywords: product; methylbenzyl; products; bis; transfer fluid
Prior art date: 1991-02-22

Application number

NO920652A

Other languages

English (en)

Norwegian (no)

Other versions

NO920652L (no

NO920652D0 (no

Inventor

Raymond Commandeur

Jean-Pierre Sarron

Original Assignee

Atochem

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.)

1991-02-22

Filing date

1992-02-19

Publication date

1997-08-25

1992-02-19 Application filed by Atochem filed Critical Atochem

1992-02-19 Publication of NO920652D0 publication Critical patent/NO920652D0/no

1992-08-24 Publication of NO920652L publication Critical patent/NO920652L/no

1997-08-25 Publication of NO300979B1 publication Critical patent/NO300979B1/no

Links

239000012530 fluid Substances 0.000 title abstract description 10
125000006178 methyl benzyl group Chemical group 0.000 title 1
150000003738 xylenes Chemical class 0.000 title 1
239000013529 heat transfer fluid Substances 0.000 claims abstract description 5
239000000203 mixture Substances 0.000 claims description 24
150000001875 compounds Chemical class 0.000 claims description 4
125000002619 bicyclic group Chemical group 0.000 claims 1
RIGGBTNEASBFER-UHFFFAOYSA-N 1,2-dimethyl-3,4-bis(1-phenylethyl)benzene Chemical group C=1C=C(C)C(C)=C(C(C)C=2C=CC=CC=2)C=1C(C)C1=CC=CC=C1 RIGGBTNEASBFER-UHFFFAOYSA-N 0.000 abstract description 4
GNPWYHFXSMINJQ-UHFFFAOYSA-N 1,2-dimethyl-3-(1-phenylethyl)benzene Chemical group C=1C=CC(C)=C(C)C=1C(C)C1=CC=CC=C1 GNPWYHFXSMINJQ-UHFFFAOYSA-N 0.000 abstract description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 22
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
238000009835 boiling Methods 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 4
239000007789 gas Substances 0.000 description 4
238000010438 heat treatment Methods 0.000 description 4
239000001257 hydrogen Substances 0.000 description 4
229910052739 hydrogen Inorganic materials 0.000 description 4
239000002655 kraft paper Substances 0.000 description 4
239000007788 liquid Substances 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
239000008096 xylene Substances 0.000 description 4
125000001931 aliphatic group Chemical group 0.000 description 3
238000004458 analytical method Methods 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
238000005660 chlorination reaction Methods 0.000 description 3
238000004587 chromatography analysis Methods 0.000 description 3
238000009833 condensation Methods 0.000 description 3
230000005494 condensation Effects 0.000 description 3
238000004821 distillation Methods 0.000 description 3
238000003756 stirring Methods 0.000 description 3
PKQYSCBUFZOAPE-UHFFFAOYSA-N 1,2-dibenzyl-3-methylbenzene Chemical compound C=1C=CC=CC=1CC=1C(C)=CC=CC=1CC1=CC=CC=C1 PKQYSCBUFZOAPE-UHFFFAOYSA-N 0.000 description 2
GTLWADFFABIGAE-UHFFFAOYSA-N 1-chloroethylbenzene Chemical compound CC(Cl)C1=CC=CC=C1 GTLWADFFABIGAE-UHFFFAOYSA-N 0.000 description 2
ZKVLFPCUFYGJDF-UHFFFAOYSA-N 2,4-diphenylpentan-3-ylbenzene Chemical compound C=1C=CC=CC=1C(C)C(C=1C=CC=CC=1)C(C)C1=CC=CC=C1 ZKVLFPCUFYGJDF-UHFFFAOYSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
239000013078 crystal Substances 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
125000005023 xylyl group Chemical group 0.000 description 2
WSSNQXJVTQOUMV-UHFFFAOYSA-N 1,2-dibenzyl-3,4-dimethylbenzene Chemical group C=1C=CC=CC=1CC1=C(C)C(C)=CC=C1CC1=CC=CC=C1 WSSNQXJVTQOUMV-UHFFFAOYSA-N 0.000 description 1
229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
150000001335 aliphatic alkanes Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
239000003708 ampul Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
229940073608 benzyl chloride Drugs 0.000 description 1
-1 bis(methylenebenzyl)xylene Chemical group 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
239000002826 coolant Substances 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
238000011010 flushing procedure Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
230000000977 initiatory effect Effects 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
239000011707 mineral Substances 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
230000000704 physical effect Effects 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
238000001577 simple distillation Methods 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007790 solid phase Substances 0.000 description 1
239000000126 substance 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
- 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

Landscapes

Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Chemical Kinetics & Catalysis (AREA)
Combustion & Propulsion (AREA)
Thermal Sciences (AREA)
Physics & Mathematics (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Lubricants (AREA)
Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Detergent Compositions (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

NO920652A 1991-02-22 1992-02-19 Anvendelse av mono- og bis(metylbenzyl)xylenisomerer som termisk overföringsfluid NO300979B1 (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR9102172A FR2673189A1 (fr)	1991-02-22	1991-02-22	Utilisation d'isomeres de mono et bis(methylbenzyl)xylene comme fluide de transfert technique.

Publications (3)

Publication Number	Publication Date
NO920652D0 NO920652D0 (no)	1992-02-19
NO920652L NO920652L (no)	1992-08-24
NO300979B1 true NO300979B1 (no)	1997-08-25

Family

ID=9410013

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO920652A NO300979B1 (no)	1991-02-22	1992-02-19	Anvendelse av mono- og bis(metylbenzyl)xylenisomerer som termisk overföringsfluid

Country Status (16)

Country	Link
US (2)	US5384058A (de)
EP (1)	EP0500435B1 (de)
JP (1)	JPH0786195B2 (de)
KR (1)	KR100192019B1 (de)
CN (1)	CN1071783C (de)
AT (1)	ATE136924T1 (de)
CA (1)	CA2061433C (de)
DE (1)	DE69209868T2 (de)
DK (1)	DK0500435T3 (de)
ES (1)	ES2086678T3 (de)
FI (1)	FI103128B (de)
FR (1)	FR2673189A1 (de)
GR (1)	GR3020324T3 (de)
IE (1)	IE73641B1 (de)
NO (1)	NO300979B1 (de)
TW (1)	TW203097B (de)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2673189A1 (fr) *	1991-02-22	1992-08-28	Atochem	Utilisation d'isomeres de mono et bis(methylbenzyl)xylene comme fluide de transfert technique.
DE69535636T2 (de) *	1994-09-30	2008-08-28	Arkema France	Verwendung für Verteilertransformatoren von einer dielektrischen Zusammensetzung, basierend auf Polyarylalkanen mit verbesserten dielektrischen Eigenschaften
FR2807059B1 (fr) *	2000-03-29	2002-05-17	Atofina	Fluide de transfert de chaleur a base de polyphenylmethanes ayant une stabilite thermique amelioree
FR2818280B1 (fr) *	2000-12-19	2003-01-17	Atofina	Formulations de peinture en dispersions aqueuses comprenant une composition de polyarylalcanes comme agent de coalescence

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2933450A (en) *	1956-07-18	1960-04-19	Olin Mathieson	Heat-exchange fluid compositions
DE1419604A1 (de) *	1961-06-12	1969-05-14	Bergwerksverband Gmbh	Verwendung fluessiger hochsiedender aromatischer Kohlenwasserstoffe als Waermeuebertragungsmittel
JPS5436154B1 (de) *	1971-07-08	1979-11-07
JPS4895599A (de) *	1972-03-17	1973-12-07
JPS5037049B2 (de) *	1972-11-15	1975-11-29
JPS52127904A (en) *	1976-04-20	1977-10-27	Nippon Oil Co Ltd	Oil composition for refrigerator
JPS5540726A (en) *	1978-09-19	1980-03-22	Nippon Oil Co Ltd	Fluid for traction drive
CA1194284A (en) *	1982-09-16	1985-10-01	Atsushi Sato	Electrical insulating oil and oil-filled electrical appliances
FR2618142B1 (fr) *	1987-07-16	1989-10-06	Atochem	Compositions d'oligomeres de polyarylalcanes contenant des motifs xylene et leur procede de fabrication
FR2673189A1 (fr) *	1991-02-22	1992-08-28	Atochem	Utilisation d'isomeres de mono et bis(methylbenzyl)xylene comme fluide de transfert technique.

1991
- 1991-02-22 FR FR9102172A patent/FR2673189A1/fr active Pending
1992
- 1992-02-14 EP EP92400407A patent/EP0500435B1/de not_active Expired - Lifetime
- 1992-02-14 DE DE69209868T patent/DE69209868T2/de not_active Expired - Fee Related
- 1992-02-14 AT AT92400407T patent/ATE136924T1/de not_active IP Right Cessation
- 1992-02-14 ES ES92400407T patent/ES2086678T3/es not_active Expired - Lifetime
- 1992-02-14 DK DK92400407.0T patent/DK0500435T3/da active
- 1992-02-17 IE IE920501A patent/IE73641B1/en not_active IP Right Cessation
- 1992-02-18 CA CA002061433A patent/CA2061433C/fr not_active Expired - Fee Related
- 1992-02-19 NO NO920652A patent/NO300979B1/no unknown
- 1992-02-20 JP JP4070385A patent/JPH0786195B2/ja not_active Expired - Fee Related
- 1992-02-21 FI FI920767A patent/FI103128B/fi not_active IP Right Cessation
- 1992-02-22 CN CN92101121A patent/CN1071783C/zh not_active Expired - Fee Related
- 1992-02-22 KR KR1019920002737A patent/KR100192019B1/ko not_active Expired - Fee Related
- 1992-03-11 TW TW081101857A patent/TW203097B/zh active
1993
- 1993-04-20 US US08/090,441 patent/US5384058A/en not_active Expired - Lifetime
1994
- 1994-08-03 US US08/283,183 patent/US5593613A/en not_active Expired - Fee Related
1996
- 1996-06-24 GR GR960401693T patent/GR3020324T3/el unknown

Also Published As

Publication number	Publication date
FI920767L (fi)	1992-08-23
DE69209868D1 (de)	1996-05-23
EP0500435B1 (de)	1996-04-17
JPH0786195B2 (ja)	1995-09-20
FI103128B1 (fi)	1999-04-30
IE920501A1 (en)	1992-08-26
CA2061433C (fr)	2003-07-15
FR2673189A1 (fr)	1992-08-28
US5593613A (en)	1997-01-14
DE69209868T2 (de)	1996-11-28
FI103128B (fi)	1999-04-30
KR920016578A (ko)	1992-09-25
GR3020324T3 (en)	1996-09-30
NO920652L (no)	1992-08-24
JPH06166866A (ja)	1994-06-14
TW203097B (de)	1993-04-01
FI920767A0 (fi)	1992-02-21
CA2061433A1 (fr)	1993-08-19
NO920652D0 (no)	1992-02-19
KR100192019B1 (ko)	1999-06-15
US5384058A (en)	1995-01-24
ES2086678T3 (es)	1996-07-01
IE73641B1 (en)	1997-06-18
CN1064300A (zh)	1992-09-09
EP0500435A1 (de)	1992-08-26
CN1071783C (zh)	2001-09-26
ATE136924T1 (de)	1996-05-15
DK0500435T3 (da)	1996-08-12

Publication	Publication Date	Title
NO164516B (no)	1990-07-09	Fremgangsmaate for fraksjonering av en gassblanding.
Blum et al.	1995	Tellurium-Mediated Halogen Transfer from Polyhaloalkanes to Diyne Acceptors
KR100192019B1 (ko)	1999-06-15	열 전달 유체용 모노- 및 비스(메틸벤질)크실렌 이성질체
JP5217008B2 (ja)	2013-06-19	スルホン酸無水物の調製方法
US3624169A (en)	1971-11-30	Process for chlorinating olefines
NO171973B (no)	1993-02-15	Blanding paa basis av polyfenylmetaner og deres anvendelsesom dielektrikum
US5821393A (en)	1998-10-13	Process for the preparation of aromatic bromoalkyl-substituted hydrocarbon compounds
CN100391917C (zh)	2008-06-04	含有间-和对-二氯苯的混合物的分离方法
US3689582A (en)	1972-09-05	Process for recovering dichloroethane in oxychlorination process
Ohno et al.	1993	Isolated carbon-deuterium stretching vibrations as a tool for conformational analysis of alkyl chains. Raman and infrared spectra of 1-bromoalkanes-1-d1 and-2-d1
US2397653A (en)	1946-04-02	Distillation of polymerizable compounds
US4100212A (en)	1978-07-11	Process for chlorinating linear paraffins
US9475697B2 (en)	2016-10-25	Removal of bromine from gaseous hydrogen bromide
US1202282A (en)	1916-10-24	Process of producing 2-chlor-isopentane.
NO328017B1 (no)	2009-11-09	Mono- og polybenzyl-1,2,3,4-tetrahydronaftalenblandinger, anvendelse av blandingene eller en blanding av monobenzyl-1,2,3,4-tetrahydronaftalenisomerer som varmeoverforingsfluid, samt fremgangsmate for fremstilling av blandingene
US2464769A (en)	1949-03-15	Separating alkyl benzenes from admixture with paraffins and naphthenes
Finger et al.	1972	Fluorination of 1, 2, 3, 4-and 1, 2, 3, 5-tetrahalobenzenes with potassium fluoride in dimethyl sulfone
Heller	1952	The Racemization of d (+)-3-Methylhexane1
US1402338A (en)	1922-01-03	Apparatus for the production of halogenated hydrocarbons
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US3592871A (en)	1971-07-13	Process for separating an alkylate-containing hydrocarbon mixture utilizing a stripping and partial condensation system
NO173231B (no)	1993-08-09	Fremgangsmaate for separering av to isomerer og dens anvendelse ved rensing av 1-fenyl 2-brometan
Boocock et al.	1963	230. The synthesis and reactions of branched-chain hydrocarbons. Part XV. Free-radical chlorination in the liquid phase
McBee et al.	1947	Fluorinated derivatives of p-ethyltoluene
Neher	1941	Chlorination of Methane and Ethane