DE2113335A1 - Verfahren zur Herstellung von Azethylen enthaltenden,zur Alkinolsynthese brauchbaren Loesungen und Verfahren zur Alkinolsynthese unter Benutzung dieser Loesungen - Google Patents
Verfahren zur Herstellung von Azethylen enthaltenden,zur Alkinolsynthese brauchbaren Loesungen und Verfahren zur Alkinolsynthese unter Benutzung dieser LoesungenInfo
- Publication number
- DE2113335A1 DE2113335A1 DE19712113335 DE2113335A DE2113335A1 DE 2113335 A1 DE2113335 A1 DE 2113335A1 DE 19712113335 DE19712113335 DE 19712113335 DE 2113335 A DE2113335 A DE 2113335A DE 2113335 A1 DE2113335 A1 DE 2113335A1
- Authority
- DE
- Germany
- Prior art keywords
- acetylene
- synthesis
- ammonia
- acetone
- range
- 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.)
- Pending
Links
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 title claims description 68
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 title claims description 68
- 238000000034 method Methods 0.000 title claims description 51
- 238000003786 synthesis reaction Methods 0.000 title claims description 31
- 230000015572 biosynthetic process Effects 0.000 title claims description 29
- 238000002360 preparation method Methods 0.000 title description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 66
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 51
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 29
- 239000005977 Ethylene Substances 0.000 claims description 29
- 229910021529 ammonia Inorganic materials 0.000 claims description 25
- 238000010521 absorption reaction Methods 0.000 claims description 20
- 150000002576 ketones Chemical class 0.000 claims description 13
- 239000007789 gas Substances 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 12
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 7
- 239000003054 catalyst Substances 0.000 claims description 7
- 239000008246 gaseous mixture Substances 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 239000003513 alkali Substances 0.000 claims description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 5
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 2
- 239000011541 reaction mixture Substances 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 150000001339 alkali metal compounds Chemical class 0.000 claims 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 1
- 239000000047 product Substances 0.000 description 13
- 238000004230 steam cracking Methods 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- 238000010586 diagram Methods 0.000 description 7
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 238000001816 cooling Methods 0.000 description 5
- JQZGUQIEPRIDMR-UHFFFAOYSA-N 3-methylbut-1-yn-1-ol Chemical compound CC(C)C#CO JQZGUQIEPRIDMR-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- 230000002745 absorbent Effects 0.000 description 3
- 239000002250 absorbent Substances 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- -1 kethane Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/36—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal
- C07C29/38—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal by reaction with aldehydes or ketones
- C07C29/42—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal by reaction with aldehydes or ketones with compounds containing triple carbon-to-carbon bonds, e.g. with metal-alkynes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/11—Purification; Separation; Use of additives by absorption, i.e. purification or separation of gaseous hydrocarbons with the aid of liquids
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P30/00—Technologies relating to oil refining and petrochemical industry
- Y02P30/40—Ethylene production
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Analytical Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Water Supply & Treatment (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Steroid Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT2234770 | 1970-03-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
DE2113335A1 true DE2113335A1 (de) | 1971-10-07 |
Family
ID=11195005
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19712113335 Pending DE2113335A1 (de) | 1970-03-24 | 1971-03-19 | Verfahren zur Herstellung von Azethylen enthaltenden,zur Alkinolsynthese brauchbaren Loesungen und Verfahren zur Alkinolsynthese unter Benutzung dieser Loesungen |
Country Status (18)
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR3127023A1 (fr) | 2021-09-13 | 2023-03-17 | Psa Automobiles Sa | Procede de pilotage d’un ensemble thermique de vehicule automobile |
-
1971
- 1971-03-09 FR FR7108110A patent/FR2109559A5/fr not_active Expired
- 1971-03-12 BE BE764146A patent/BE764146A/xx unknown
- 1971-03-16 CH CH373271A patent/CH533586A/fr not_active IP Right Cessation
- 1971-03-18 NO NO1043/71A patent/NO137995C/no unknown
- 1971-03-19 DE DE19712113335 patent/DE2113335A1/de active Pending
- 1971-03-22 PL PL1971147067A patent/PL83143B1/pl unknown
- 1971-03-23 CS CS2115A patent/CS167919B2/cs unknown
- 1971-03-23 HU HUSA2181A patent/HU166622B/hu unknown
- 1971-03-23 ES ES389854A patent/ES389854A1/es not_active Expired
- 1971-03-23 DD DD164215A patent/DD98501A5/xx unknown
- 1971-03-23 LU LU62845D patent/LU62845A1/xx unknown
- 1971-03-23 AT AT251371A patent/AT315811B/de not_active IP Right Cessation
- 1971-03-23 CA CA108,530A patent/CA957385A/en not_active Expired
- 1971-03-24 NL NL7103948A patent/NL7103948A/xx not_active Application Discontinuation
- 1971-03-24 SE SE7103849A patent/SE399248B/xx unknown
- 1971-03-24 ZA ZA711910A patent/ZA711910B/xx unknown
- 1971-03-24 RO RO66376A patent/RO60592A/ro unknown
- 1971-04-19 GB GB2508071*A patent/GB1342167A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
NO137995B (no) | 1978-02-27 |
CH533586A (fr) | 1973-03-15 |
SE399248B (sv) | 1978-02-06 |
LU62845A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1971-08-24 |
ZA711910B (en) | 1971-12-29 |
GB1342167A (en) | 1973-12-25 |
NO137995C (no) | 1978-06-07 |
AT315811B (de) | 1974-06-10 |
CA957385A (en) | 1974-11-05 |
DD98501A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1973-06-20 |
BE764146A (fr) | 1971-08-02 |
HU166622B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1975-04-28 |
FR2109559A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1972-05-26 |
PL83143B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1975-12-31 |
NL7103948A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1971-09-28 |
CS167919B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-05-28 |
RO60592A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-09-15 |
ES389854A1 (es) | 1974-05-16 |
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