NO130641B - - Google Patents

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Info

Publication number: NO130641B
Authority: NO; Norway
Prior art keywords: benzene; chlorine; reactor; reaction; carbon tetrachloride
Prior art date: 1969-01-30

Application number

NO00084/70A

Other languages

English (en)

Norwegian (no)

Other versions

NO130641C (ja

Inventor

H Krekeler

H Meidert

W Riemenschneider

L Hoernig

Original Assignee

Hoechst Ag

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.)

1969-01-30

Filing date

1970-01-09

Publication date

1974-10-07

1970-01-09 Application filed by Hoechst Ag filed Critical Hoechst Ag

1974-10-07 Publication of NO130641B publication Critical patent/NO130641B/no

1975-01-15 Publication of NO130641C publication Critical patent/NO130641C/no

Links

UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 150
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 74
238000006243 chemical reaction Methods 0.000 claims description 68
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical class [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 43
239000000460 chlorine Chemical class 0.000 claims description 43
229910052801 chlorine Chemical class 0.000 claims description 43
239000000203 mixture Substances 0.000 claims description 35
238000000034 method Methods 0.000 claims description 20
150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 16
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 11
230000007306 turnover Effects 0.000 claims description 9
125000001931 aliphatic group Chemical group 0.000 claims description 6
230000008569 process Effects 0.000 claims description 6
229930195733 hydrocarbon Natural products 0.000 claims description 5
150000002430 hydrocarbons Chemical class 0.000 claims description 5
238000004519 manufacturing process Methods 0.000 claims description 5
238000005260 corrosion Methods 0.000 claims description 4
230000007797 corrosion Effects 0.000 claims description 4
239000003054 catalyst Substances 0.000 claims description 3
CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 description 18
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 10
238000010438 heat treatment Methods 0.000 description 10
239000007789 gas Substances 0.000 description 9
239000006227 byproduct Substances 0.000 description 7
230000000052 comparative effect Effects 0.000 description 7
239000007858 starting material Substances 0.000 description 7
230000015572 biosynthetic process Effects 0.000 description 5
239000007788 liquid Substances 0.000 description 5
238000002844 melting Methods 0.000 description 5
230000008018 melting Effects 0.000 description 5
238000002156 mixing Methods 0.000 description 5
229910052759 nickel Inorganic materials 0.000 description 5
238000001816 cooling Methods 0.000 description 4
150000002894 organic compounds Chemical class 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 3
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 3
150000007824 aliphatic compounds Chemical class 0.000 description 3
230000008901 benefit Effects 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
229910000041 hydrogen chloride Inorganic materials 0.000 description 3
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
239000000463 material Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
230000009467 reduction Effects 0.000 description 3
229950011008 tetrachloroethylene Drugs 0.000 description 3
UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 3
QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
229910000831 Steel Inorganic materials 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000011109 contamination Methods 0.000 description 2
JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 2
VHHHONWQHHHLTI-UHFFFAOYSA-N hexachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Cl)Cl VHHHONWQHHHLTI-UHFFFAOYSA-N 0.000 description 2
239000000376 reactant Substances 0.000 description 2
238000000926 separation method Methods 0.000 description 2
239000010935 stainless steel Substances 0.000 description 2
229910001220 stainless steel Inorganic materials 0.000 description 2
239000010959 steel Substances 0.000 description 2
SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
KFUSEUYYWQURPO-UHFFFAOYSA-N 1,2-dichloroethene Chemical compound ClC=CCl KFUSEUYYWQURPO-UHFFFAOYSA-N 0.000 description 1
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical class CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
150000001335 aliphatic alkanes Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
150000001345 alkine derivatives Chemical class 0.000 description 1
239000000956 alloy Substances 0.000 description 1
229910045601 alloy Inorganic materials 0.000 description 1
OJYGBLRPYBAHRT-UHFFFAOYSA-N alphachloralose Chemical compound O1C(C(Cl)(Cl)Cl)OC2C(O)C(C(O)CO)OC21 OJYGBLRPYBAHRT-UHFFFAOYSA-N 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene group Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
235000013844 butane Nutrition 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
238000005660 chlorination reaction Methods 0.000 description 1
150000001804 chlorine Chemical class 0.000 description 1
DIWKDXFZXXCDLF-UHFFFAOYSA-N chloroethyne Chemical class ClC#C DIWKDXFZXXCDLF-UHFFFAOYSA-N 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000000567 combustion gas Substances 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
239000000356 contaminant Substances 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000005485 electric heating Methods 0.000 description 1
239000003344 environmental pollutant Substances 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
230000020169 heat generation Effects 0.000 description 1
230000006872 improvement Effects 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
229960002809 lindane Drugs 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical class CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
231100000719 pollutant Toxicity 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
125000004805 propylene group Chemical class [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
239000012495 reaction gas Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000000859 sublimation Methods 0.000 description 1
230000008022 sublimation Effects 0.000 description 1
239000000126 substance Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/361—Preparation of halogenated hydrocarbons by reactions involving a decrease in the number of carbon atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

NO84/70A 1969-01-30 1970-01-09 NO130641C (ja)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE1904426A DE1904426C3 (de)	1969-01-30	1969-01-30	Verfahren zur Herstellung von Tetrachlorkohlenstoff aus Benzol und Chlor

Publications (2)

Publication Number	Publication Date
NO130641B true NO130641B (ja)	1974-10-07
NO130641C NO130641C (ja)	1975-01-15

Family

ID=5723729

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO84/70A NO130641C (ja)	1969-01-30	1970-01-09

Country Status (16)

Country	Link
US (1)	US3676508A (ja)
JP (1)	JPS5010285B1 (ja)
BE (1)	BE745271R (ja)
BG (1)	BG17510A3 (ja)
BR (1)	BR7016194D0 (ja)
CA (1)	CA952542A (ja)
CS (1)	CS157081B4 (ja)
DE (1)	DE1904426C3 (ja)
ES (1)	ES375972A2 (ja)
FR (1)	FR2045757B2 (ja)
GB (1)	GB1292903A (ja)
NL (1)	NL6919491A (ja)
NO (1)	NO130641C (ja)
PL (1)	PL80453B3 (ja)
YU (1)	YU20870A (ja)
ZA (1)	ZA70592B (ja)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP6022770B2 (ja) *	2008-10-13	2016-11-09	ブルーキューブアイピーエルエルシー	塩素化及び／又はフッ素化プロペンの製造方法
KR20120093857A (ko) *	2009-10-09	2012-08-23	다우 글로벌 테크놀로지스 엘엘씨	염화 및/또는 불화 프로펜의 제조 방법
CN105664811B (zh) *	2009-10-09	2018-10-09	蓝立方知识产权公司	生产氯化和/或氟化丙烯和高级烯烃的绝热活塞流反应器及方法
CN102596387B (zh)	2009-10-09	2015-11-25	陶氏环球技术有限责任公司	生产氯化和/或氟化丙烯和高级烯烃的等温多管反应器和方法
WO2011044536A1 (en) *	2009-10-09	2011-04-14	Dow Global Technologies, Inc	Process for the production of chlorinated and/or fluorinated propenes and higher alkenes
WO2012166393A1 (en)	2011-05-31	2012-12-06	Dow Global Technologies, Llc	Process for the production of chlorinated propenes
WO2012166394A1 (en)	2011-05-31	2012-12-06	Dow Global Technologies, Llc	Process for the production of chlorinated propenes
ES2721451T3 (es)	2011-06-08	2019-07-31	Dow Agrosciences Llc	Procedimiento para la producción de propenos clorados y/o fluorados
JP6166261B2 (ja)	2011-08-07	2017-07-19	ブルーキューブアイピーエルエルシー	塩素化プロペンの製造方法
CN103717559A (zh)	2011-08-07	2014-04-09	陶氏环球技术有限责任公司	生产氯化的丙烯的方法
EP2782889B1 (en)	2011-11-21	2016-12-21	Blue Cube IP LLC	Process for the production of chlorinated alkanes
US9199899B2 (en)	2011-12-02	2015-12-01	Blue Cube Ip Llc	Process for the production of chlorinated alkanes
JP6050375B2 (ja)	2011-12-02	2016-12-21	ブルーキューブアイピーエルエルシー	クロロアルカンの製造方法
JP6170068B2 (ja)	2011-12-13	2017-07-26	ブルーキューブアイピーエルエルシー	塩素化プロパン及びプロペンの製造方法
IN2014CN04418A (ja)	2011-12-22	2015-09-04	Dow Global Technologies Llc
BR112014015123A2 (pt)	2011-12-23	2017-06-13	Dow Global Technologies Llc	processo para a produção de um ou mais alcenos ou compostos aromáticos
EP2897930A1 (en)	2012-09-20	2015-07-29	Dow Global Technologies LLC	Process for the production of chlorinated propenes
CN104755448A (zh)	2012-09-20	2015-07-01	陶氏环球技术有限公司	用于制造氯化丙烯的方法
EP2900364B1 (en)	2012-09-30	2018-06-13	Blue Cube IP LLC	Weir quench and processes incorporating the same
WO2014066083A1 (en)	2012-10-26	2014-05-01	Dow Global Technologies, Llc	Mixer and reactor and process incorporating the same
US9512053B2 (en)	2012-12-18	2016-12-06	Blue Cube Ip Llc	Process for the production of chlorinated propenes
US9475740B2 (en)	2012-12-19	2016-10-25	Blue Cube Ip Llc	Process for the production of chlorinated propenes
US9382176B2 (en)	2013-02-27	2016-07-05	Blue Cube Ip Llc	Process for the production of chlorinated propenes
US9403741B2 (en)	2013-03-09	2016-08-02	Blue Cube Ip Llc	Process for the production of chlorinated alkanes
PT3481797T (pt) *	2016-07-05	2021-05-13	Occidental Chem Co	Fotocloração de clorofórmio em tetracloreto de carbono
EP3908564A4 (en)	2019-01-10	2022-10-26	Occidental Chemical Corporation	PHOTOCHLORINATION OF PARTIALLY CHLORINED CHLOROMETHANE TO CARBON TETRACHLORIDE

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IT581918A (ja) *	1956-10-23

1969
- 1969-01-30 DE DE1904426A patent/DE1904426C3/de not_active Expired
- 1969-12-29 NL NL6919491A patent/NL6919491A/xx unknown
1970
- 1970-01-09 NO NO84/70A patent/NO130641C/no unknown
- 1970-01-12 CS CS22370*#A patent/CS157081B4/cs unknown
- 1970-01-21 US US4748A patent/US3676508A/en not_active Expired - Lifetime
- 1970-01-22 BR BR216194/70A patent/BR7016194D0/pt unknown
- 1970-01-23 GB GB3432/70A patent/GB1292903A/en not_active Expired
- 1970-01-28 ES ES375972A patent/ES375972A2/es not_active Expired
- 1970-01-28 ZA ZA700592A patent/ZA70592B/xx unknown
- 1970-01-29 CA CA073,417A patent/CA952542A/en not_active Expired
- 1970-01-29 YU YU00208/70A patent/YU20870A/xx unknown
- 1970-01-29 PL PL1970138465A patent/PL80453B3/pl unknown
- 1970-01-30 JP JP45007820A patent/JPS5010285B1/ja active Pending
- 1970-01-30 BG BG013847A patent/BG17510A3/xx unknown
- 1970-01-30 FR FR707003310A patent/FR2045757B2/fr not_active Expired
- 1970-01-30 BE BE745271D patent/BE745271R/xx active

Also Published As

Publication number	Publication date
DE1904426C3 (de)	1974-02-28
JPS5010285B1 (ja)	1975-04-19
DE1904426B2 (de)	1973-07-26
BR7016194D0 (pt)	1973-01-16
YU20870A (en)	1978-06-30
NO130641C (ja)	1975-01-15
CS157081B4 (ja)	1974-08-23
CA952542A (en)	1974-08-06
ZA70592B (en)	1971-03-31
NL6919491A (ja)	1970-08-03
ES375972A2 (es)	1972-07-01
DE1904426A1 (de)	1970-09-24
FR2045757A2 (ja)	1971-03-05
BE745271R (fr)	1970-07-30
GB1292903A (en)	1972-10-18
FR2045757B2 (ja)	1974-03-01
PL80453B3 (en)	1975-08-30
US3676508A (en)	1972-07-11
BG17510A3 (bg)	1973-11-10

Publication	Publication Date	Title
NO130641B (ja)	1974-10-07
US4661648A (en)	1987-04-28	Process for carrying out substitution chlorination reactions of organic compounds by means of molecular chlorine in the presence of a chlorinated product serving as a radical initiator, and radical initiators used in such a process
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JPH0236576B2 (ja)	1990-08-17
US4851597A (en)	1989-07-25	Process for the thermal cleavage of 1,2-dichloroethane
AU611016B2 (en)	1991-05-30	Process for the synthesis of ferric chloride
US3475504A (en)	1969-10-28	Process for the chlorination of olefinic hydrocarbons and ethylenically unsaturated chlorohydrocarbons
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US2034292A (en)	1936-03-17	Production of carbon chlorides
US3330877A (en)	1967-07-11	Process for the chlorination of unsaturated hydrocarbons and unsaturated chlorohydrocarbons
EP1528052B1 (en)	2013-07-31	Process for the production of 4-amino-3,5-dichlorobenzotrifluoride with high purity commercial products being obtained in parallel
US3344197A (en)	1967-09-26	Production of 1, 1, 2-trichloroethane from 1, 2-dichloroethane and chlorine
JPH07233102A (ja)	1995-09-05	有機化合物を液相フッ素化する方法
US4849561A (en)	1989-07-18	Liquid phase process for dehydrochlorination of haloalkanes in the presence of an initiator based on an organic chlorinated product
US3644542A (en)	1972-02-22	Benzene oxychlorination
US3928479A (en)	1975-12-23	Process for the manufacture of carbon tetrachloride
US3651157A (en)	1972-03-21	Process for the manufacture of carbontetrachloride