NO764202L - - Google Patents
Info
- Publication number
- NO764202L NO764202L NO764202A NO764202A NO764202L NO 764202 L NO764202 L NO 764202L NO 764202 A NO764202 A NO 764202A NO 764202 A NO764202 A NO 764202A NO 764202 L NO764202 L NO 764202L
- Authority
- NO
- Norway
- Prior art keywords
- reaction
- gas
- hydrogen
- residue
- ammonia
- Prior art date
Links
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 82
- 239000007789 gas Substances 0.000 claims description 76
- 239000003054 catalyst Substances 0.000 claims description 65
- 238000006243 chemical reaction Methods 0.000 claims description 63
- 238000000034 method Methods 0.000 claims description 58
- 239000001257 hydrogen Substances 0.000 claims description 56
- 229910052739 hydrogen Inorganic materials 0.000 claims description 56
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 49
- 229910021529 ammonia Inorganic materials 0.000 claims description 42
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 34
- -1 ether amines Chemical group 0.000 claims description 28
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 25
- 230000035484 reaction time Effects 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
- 230000008569 process Effects 0.000 claims description 12
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 229910017052 cobalt Inorganic materials 0.000 claims description 8
- 239000010941 cobalt Substances 0.000 claims description 8
- 229910052759 nickel Inorganic materials 0.000 claims description 8
- 239000012071 phase Substances 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 238000006297 dehydration reaction Methods 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 229920006395 saturated elastomer Polymers 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 239000011261 inert gas Substances 0.000 claims description 3
- 239000007791 liquid phase Substances 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 239000012495 reaction gas Substances 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims description 2
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims description 2
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 238000007098 aminolysis reaction Methods 0.000 description 16
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 230000007935 neutral effect Effects 0.000 description 11
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 9
- 150000001298 alcohols Chemical class 0.000 description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- 238000007792 addition Methods 0.000 description 6
- 239000000706 filtrate Substances 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 5
- 239000006227 byproduct Substances 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 150000002431 hydrogen Chemical class 0.000 description 5
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
- 150000002191 fatty alcohols Chemical class 0.000 description 4
- 238000000926 separation method Methods 0.000 description 4
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 230000007306 turnover Effects 0.000 description 4
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 3
- XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 3
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005909 Kieselgur Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229940055577 oleyl alcohol Drugs 0.000 description 3
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 101500021084 Locusta migratoria 5 kDa peptide Proteins 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- 239000007868 Raney catalyst Substances 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 125000005262 alkoxyamine group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 125000005429 oxyalkyl group Chemical group 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- QQGRFMIMXPWKPM-UHFFFAOYSA-N 2,3,4-tributylphenol Chemical class CCCCC1=CC=C(O)C(CCCC)=C1CCCC QQGRFMIMXPWKPM-UHFFFAOYSA-N 0.000 description 1
- QDTDKYHPHANITQ-UHFFFAOYSA-N 7-methyloctan-1-ol Chemical compound CC(C)CCCCCCO QDTDKYHPHANITQ-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical class ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 239000004439 Isononyl alcohol Substances 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical group [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 238000005576 amination reaction Methods 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 150000005840 aryl radicals Chemical group 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/321—Polymers modified by chemical after-treatment with inorganic compounds
- C08G65/325—Polymers modified by chemical after-treatment with inorganic compounds containing nitrogen
- C08G65/3255—Ammonia
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2555895A DE2555895B2 (de) | 1975-12-12 | 1975-12-12 | Sekundäre Ätheramine und Verfahren zu deren Herstellung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO764202L true NO764202L (pt) | 1977-06-14 |
Family
ID=5964142
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO764202A NO764202L (pt) | 1975-12-12 | 1976-12-10 |
Country Status (16)
| Country | Link |
|---|---|
| JP (1) | JPS5273807A (pt) |
| AU (1) | AU2049776A (pt) |
| BE (1) | BE849348A (pt) |
| BR (1) | BR7608263A (pt) |
| DE (1) | DE2555895B2 (pt) |
| DK (1) | DK555176A (pt) |
| ES (1) | ES453996A1 (pt) |
| FI (1) | FI763546A (pt) |
| FR (1) | FR2334656A1 (pt) |
| IT (1) | IT1070015B (pt) |
| LU (1) | LU76364A1 (pt) |
| NL (1) | NL7613589A (pt) |
| NO (1) | NO764202L (pt) |
| PT (1) | PT65952B (pt) |
| SE (1) | SE7613947L (pt) |
| ZA (1) | ZA767359B (pt) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2642517A1 (de) * | 1976-09-22 | 1978-03-23 | Hoechst Ag | Salze sekundaerer aetheramine und deren verwendung als praeparationsmittel fuer synthesefasern |
| DE2843659C3 (de) | 1978-10-06 | 1984-05-24 | Hoechst Ag, 6230 Frankfurt | Verwendung quaternierter Etheramine als Faserpräparationsmittel |
| FR2455570A1 (fr) * | 1979-05-03 | 1980-11-28 | Rhone Poulenc Ind | Procede de preparation de tris(ether-amines) et tris(ether-amines) ainsi obtenues |
| DE3026127A1 (de) * | 1980-07-10 | 1982-02-18 | Hoechst Ag, 6000 Frankfurt | Bisphenolderivate, verfahren zu ihrer herstellung und ihre verwendung als tenside |
| DE3826608A1 (de) * | 1988-08-05 | 1990-02-08 | Basf Ag | Polyetheramine oder polyetheraminderivate enthaltende kraftstoffe fuer ottomotoren |
| CA2032449A1 (en) * | 1990-01-24 | 1991-07-25 | John F. Knifton | "twin-tailed" polyoxyalkylene tertiary amines |
| DE10109483A1 (de) | 2001-02-28 | 2002-09-05 | Clariant Gmbh | Oxalkylierungsprodukte hergestellt aus Epoxiden und Aminen und deren Verwendung in Pigmentpräparationen |
| CN111875512B (zh) * | 2019-11-12 | 2021-09-14 | 四川大学 | 含醚键的仲胺、酰胺荚醚配体及其制备方法与应用 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3373204A (en) * | 1964-04-15 | 1968-03-12 | Atlas Chem Ind | Process for preparing oxyalkylene amines |
| US3440029A (en) * | 1964-05-20 | 1969-04-22 | Dow Chemical Co | Gasoline containing anti-icing additive |
| DE2555896C3 (de) * | 1975-12-12 | 1982-01-28 | Hoechst Ag, 6000 Frankfurt | Sekundäre Ätheraminacetate Verfahren zu deren Herstellung und deren Verwendung als Präparationsmittel für Synthesefasern |
-
1975
- 1975-12-12 DE DE2555895A patent/DE2555895B2/de not_active Withdrawn
-
1976
- 1976-12-06 ES ES453996A patent/ES453996A1/es not_active Expired
- 1976-12-07 NL NL7613589A patent/NL7613589A/xx not_active Application Discontinuation
- 1976-12-09 FI FI763546A patent/FI763546A/fi not_active Application Discontinuation
- 1976-12-09 BR BR7608263A patent/BR7608263A/pt unknown
- 1976-12-10 NO NO764202A patent/NO764202L/no unknown
- 1976-12-10 LU LU76364A patent/LU76364A1/xx unknown
- 1976-12-10 ZA ZA767359A patent/ZA767359B/xx unknown
- 1976-12-10 SE SE7613947A patent/SE7613947L/xx unknown
- 1976-12-10 PT PT65952A patent/PT65952B/pt unknown
- 1976-12-10 JP JP51147869A patent/JPS5273807A/ja active Pending
- 1976-12-10 DK DK555176A patent/DK555176A/da not_active Application Discontinuation
- 1976-12-10 IT IT30323/76A patent/IT1070015B/it active
- 1976-12-13 AU AU20497/76A patent/AU2049776A/en not_active Expired
- 1976-12-13 BE BE173208A patent/BE849348A/xx unknown
- 1976-12-13 FR FR7637471A patent/FR2334656A1/fr not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| BE849348A (fr) | 1977-06-13 |
| BR7608263A (pt) | 1977-11-29 |
| ZA767359B (en) | 1977-11-30 |
| PT65952B (en) | 1978-07-05 |
| FR2334656A1 (fr) | 1977-07-08 |
| AU2049776A (en) | 1978-06-22 |
| DK555176A (da) | 1977-06-13 |
| DE2555895A1 (de) | 1977-06-23 |
| LU76364A1 (pt) | 1977-06-24 |
| FI763546A (pt) | 1977-06-13 |
| SE7613947L (sv) | 1977-06-13 |
| PT65952A (en) | 1977-01-01 |
| JPS5273807A (en) | 1977-06-21 |
| IT1070015B (it) | 1985-03-25 |
| ES453996A1 (es) | 1977-11-16 |
| NL7613589A (nl) | 1977-06-14 |
| DE2555895B2 (de) | 1978-11-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5792895A (en) | Process for the conversion of ethylene into but-1-ene using additives based on polymethylene glycols and derivatives thereof | |
| CN102439062B (zh) | 脂肪族聚碳酸酯的制造方法 | |
| US8329955B2 (en) | Continuous preparation of amines by nitrile compound hydrogenation | |
| JP6559067B2 (ja) | 不活性ガス又は過熱蒸気を用いた除去下におけるカルバミン酸メチル及び炭酸ジメチル（ｄｍｃ）の合成並びにそのための反応器 | |
| NO764202L (pt) | ||
| CN102260326A (zh) | 卡贝缩宫素的制备方法 | |
| CN106631684A (zh) | 一种用乙酸仲丁酯水解制备仲丁醇的方法 | |
| US4138437A (en) | Process for the preparation of tertiary aliphatic amines | |
| RO117320B1 (ro) | Procedeu de preparare a 2-alchil-6-metil-n-(1'-metoxi-2'-propil)-anilinei | |
| DK145493B (da) | Fremgangsmaade til fremstilling af tertiaere aliphatiske aminer | |
| CN102050841B (zh) | 2-丙酰基-1，10-菲咯啉缩苯胺类配合物及制备方法以及含有所述配合物的催化剂及用途 | |
| US3394192A (en) | Preparation of beta-mercaptoalkanols | |
| CN106748763A (zh) | 两釜联合相转移催化合成苯甲酸甲酯的方法 | |
| WO2007114130A9 (ja) | 二酸化炭素回収利用、移送用混合物 | |
| CN103254101B (zh) | 制备氨基甲酸甲酯的方法及设备 | |
| NO783754L (no) | Fremgangsaate for fremstilling av beta-fenyletylalkohol | |
| SU550975A3 (ru) | Способ получени вторичных алифатических аминов | |
| CN108456228A (zh) | 一种小空障有机膦配体及其制备方法与在乙烯制1-辛烯及1-己烯中的应用 | |
| US4210604A (en) | Process for preparing secondary amines from mixtures of aliphatic alcohols and nitriles | |
| CN105153218B (zh) | 一种同时提高n,o—双(三甲硅基)乙酰胺的纯度与收率的生产方法 | |
| CN209352804U (zh) | 一种盐碱液萃取-水解的乙胺生产系统 | |
| CN106397188A (zh) | 一种l‑菊苣酸的制备方法 | |
| CN113731505A (zh) | 一种乙烯齐聚催化剂体系与应用 | |
| SU452090A3 (ru) | Способ получени третичных аминов | |
| JP3651761B2 (ja) | メタノールの製造方法 |