CH208945A - Verfahren zur Herstellung ungesättigter, halogenhaltiger Propylene. - Google Patents
Verfahren zur Herstellung ungesättigter, halogenhaltiger Propylene.Info
- Publication number
- CH208945A CH208945A CH208945DA CH208945A CH 208945 A CH208945 A CH 208945A CH 208945D A CH208945D A CH 208945DA CH 208945 A CH208945 A CH 208945A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- chloride
- propylene
- halogen
- unsaturated
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 15
- 125000004805 propylene group Chemical class [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 title claims description 11
- 229910052736 halogen Inorganic materials 0.000 title claims description 6
- 150000002367 halogens Chemical class 0.000 title claims description 6
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- OSDWBNJEKMUWAV-UHFFFAOYSA-N Allyl chloride Chemical compound ClCC=C OSDWBNJEKMUWAV-UHFFFAOYSA-N 0.000 claims description 15
- KNKRKFALVUDBJE-UHFFFAOYSA-N 1,2-dichloropropane Chemical compound CC(Cl)CCl KNKRKFALVUDBJE-UHFFFAOYSA-N 0.000 claims description 11
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- -1 propylene halide Chemical class 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 150000001721 carbon Chemical group 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 19
- 229910000039 hydrogen halide Inorganic materials 0.000 description 9
- 239000012433 hydrogen halide Substances 0.000 description 9
- 230000035484 reaction time Effects 0.000 description 8
- 239000000047 product Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- 230000008901 benefit Effects 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 238000005660 chlorination reaction Methods 0.000 description 4
- 230000008030 elimination Effects 0.000 description 4
- 238000003379 elimination reaction Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 238000002474 experimental method Methods 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
- 239000010959 steel Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 235000011148 calcium chloride Nutrition 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- SNMVRZFUUCLYTO-UHFFFAOYSA-N n-propyl chloride Chemical compound CCCCl SNMVRZFUUCLYTO-UHFFFAOYSA-N 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPKPKFIWDXDAGC-NSCUHMNNSA-N (e)-1,2-dichloroprop-1-ene Chemical group C\C(Cl)=C/Cl PPKPKFIWDXDAGC-NSCUHMNNSA-N 0.000 description 1
- PNLQPWWBHXMFCA-UHFFFAOYSA-N 2-chloroprop-1-ene Chemical class CC(Cl)=C PNLQPWWBHXMFCA-UHFFFAOYSA-N 0.000 description 1
- IJJWOSAXNHWBPR-HUBLWGQQSA-N 5-[(3as,4s,6ar)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]-n-(6-hydrazinyl-6-oxohexyl)pentanamide Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)NCCCCCC(=O)NN)SC[C@@H]21 IJJWOSAXNHWBPR-HUBLWGQQSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 150000001361 allenes Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910002090 carbon oxide Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical group CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 230000001698 pyrogenic effect Effects 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/25—Preparation of halogenated hydrocarbons by splitting-off hydrogen halides from halogenated hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US163822A US2207193A (en) | 1937-09-14 | 1937-09-14 | Production of allyl type halides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH208945A true CH208945A (de) | 1940-03-15 |
Family
ID=22591726
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH208945D CH208945A (de) | 1937-09-14 | 1938-09-10 | Verfahren zur Herstellung ungesättigter, halogenhaltiger Propylene. |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US2207193A (enExample) |
| CH (1) | CH208945A (enExample) |
| FR (1) | FR843274A (enExample) |
| GB (1) | GB518325A (enExample) |
| NL (1) | NL50974C (enExample) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL59530C (enExample) * | 1941-09-12 | |||
| US5118889A (en) * | 1991-10-21 | 1992-06-02 | Shell Oil Company | Process for preparing allyl chloride |
| BR112012007914A2 (pt) | 2009-10-09 | 2019-09-24 | Dow Global Technologies Llc | reator isotérmico de tubos múltiplos, processo para produzir um propeno clorado ou fluorado e processo para preparar 2,3,3,3- tetrafluorprop-1-eno (hfo-1234yf) ou 1,3,3,3- tetrafluorprop-1-eno (hfo-1234ze) |
| WO2011044522A2 (en) * | 2009-10-09 | 2011-04-14 | Dow Global Technologies, Inc | Adiabatic plug flow reactors and processes incorporating the same |
| 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 |
| US9056808B2 (en) | 2011-05-31 | 2015-06-16 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
| EP2739595B1 (en) | 2011-08-07 | 2018-12-12 | Blue Cube IP LLC | Process for the production of chlorinated propenes |
| CA2844319A1 (en) | 2011-08-07 | 2013-02-14 | Dow Global Technologies Llc | Process for the production of chlorinated propenes |
| IN2014CN03748A (enExample) | 2011-11-21 | 2015-09-25 | Dow Global Technologies Llc | |
| CN104024187B (zh) | 2011-12-02 | 2017-04-12 | 蓝立方知识产权有限责任公司 | 生产氯化烷烃的方法 |
| CA2856545A1 (en) | 2011-12-02 | 2013-06-06 | Dow Global Technologies Llc | Process for the production of chlorinated alkanes |
| 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 |
| EP2794528B1 (en) | 2011-12-22 | 2020-02-26 | Blue Cube IP LLC | Process for the production of tetrachloromethane |
| EP2794521B1 (en) | 2011-12-23 | 2016-09-21 | Dow Global Technologies LLC | Process for the production of alkenes and/or aromatic compounds |
| WO2014046970A1 (en) | 2012-09-20 | 2014-03-27 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
| EP2897932A1 (en) | 2012-09-20 | 2015-07-29 | Dow Global Technologies LLC | Process for the production of chlorinated propenes |
| EP2900364B1 (en) | 2012-09-30 | 2018-06-13 | Blue Cube IP LLC | Weir quench and processes incorporating the same |
| EP2911773B1 (en) | 2012-10-26 | 2017-10-04 | Blue Cube IP LLC | Mixer and reactor and process incorporating the same |
| CA2893841C (en) | 2012-12-18 | 2018-07-24 | Dow Global Technologies Llc | Process for the production of chlorinated propenes |
| EP2935166A1 (en) | 2012-12-19 | 2015-10-28 | 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 |
| US11360064B2 (en) * | 2016-03-30 | 2022-06-14 | 3M Innovative Properties Company | Oxy-pyrohydrolysis system and method for total halogen analysis |
-
1937
- 1937-09-14 US US163822A patent/US2207193A/en not_active Expired - Lifetime
-
1938
- 1938-09-07 GB GB26194/38A patent/GB518325A/en not_active Expired
- 1938-09-10 FR FR843274D patent/FR843274A/fr not_active Expired
- 1938-09-10 CH CH208945D patent/CH208945A/de unknown
- 1938-09-13 NL NL89718A patent/NL50974C/xx active
Also Published As
| Publication number | Publication date |
|---|---|
| GB518325A (en) | 1940-02-23 |
| FR843274A (fr) | 1939-06-28 |
| US2207193A (en) | 1940-07-09 |
| NL50974C (enExample) | 1941-09-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CH208945A (de) | Verfahren zur Herstellung ungesättigter, halogenhaltiger Propylene. | |
| DE468402C (de) | Verfahren zur Gewinnung von Keten aus Aceton | |
| DE1668842A1 (de) | Verfahren zur Herstellung von 1,1-Dichloraethan | |
| DE2329750C2 (de) | Verfahren zur Herstellung von Hexafluorpropen durch Pyrolyse von Tetrafluoräthylen | |
| EP0656875A1 (de) | Verfahren zur herstellung von vinylchlorid | |
| DE486952C (de) | Verfahren zur Darstellung der Chlorierungsprodukte des Methans | |
| DE862895C (de) | Verfahren zur Entfernung des Halogenwasserstoffs aus den Umsetzungsprodukten halogenhaltiger Siliciumverbindungen | |
| DE801987C (de) | Verfahren zur Herstellung von Hexachloraethan | |
| DE2135908C3 (de) | Verfahren zur Herstellung von Vinylidenchlorid | |
| AT160135B (de) | Verfahren zur Herstellung von Tetrachlorkohlenstoff. | |
| DE1951165A1 (de) | Verfahren zur thermischen Perchlorierung von Kohlenwasserstoffen und partiell chlorierten Kohlenwasserstoffen | |
| DE887809C (de) | Verfahren zur Herstellung von Perchloraethylen, gegebenen-falls im Gemisch mit Tetrachlormethan, durch Chlorierung von Kohlenwasserstoffen | |
| AT165047B (de) | Verfahren zur Herstellung von organischen Fluorverbindungen | |
| DE712492C (de) | Verfahren zur Herstellung von Tetrachlorkohlenstoff | |
| AT163169B (de) | Verfahren zur Herstellung von Hexachlorbutadien | |
| DE1618531C2 (de) | Verfahren zur Herstellung von Tetrachlormethan oder Gemischen, die einen hohen Anteil Tetrachlormethan neben Perchloräthylen enthalten | |
| DE736884C (de) | Verfahren zur Herstellung von Hexachlorbutadien | |
| DE1240842B (de) | Verfahren zur Aufbereitung von hochchlorierten, spezifisch schweren Rueckstaenden, die bei der industriellen Herstellung von chlorierten Kohlenwasserstoffen anfallen | |
| AT164479B (de) | Verfahren zur Herstellung von Perchloräthylen gegebenenfalls im Gemisch mit Tetrachlormethan | |
| DE1418854C (de) | Verfahren zur thermischen Spaltung von Olefinen | |
| DE2652332A1 (de) | Verfahren zur herstellung von 1,2-dichloraethan | |
| AT229281B (de) | Verfahren zur Herstellung von Olefinen | |
| DE464320C (de) | Verfahren zur Darstellung von Chlorsubstitutionsprodukten des AEthylens | |
| DE955057C (de) | Verfahren zur Herstellung von Vinylidenchlorid und Vinylchlorid | |
| AT106813B (de) | Verfahren zum Chlorieren von Azetylen. |