BE553813A - - Google Patents
Info
- Publication number
- BE553813A BE553813A BE553813DA BE553813A BE 553813 A BE553813 A BE 553813A BE 553813D A BE553813D A BE 553813DA BE 553813 A BE553813 A BE 553813A
- Authority
- BE
- Belgium
- Prior art keywords
- ammonia
- dehydration
- catalyst
- amino
- lactam
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 38
- 150000003951 lactams Chemical class 0.000 description 21
- 229910021529 ammonia Inorganic materials 0.000 description 19
- 238000006297 dehydration reaction Methods 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 17
- 230000018044 dehydration Effects 0.000 description 16
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000006227 byproduct Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 5
- 150000002825 nitriles Chemical class 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 230000007935 neutral effect Effects 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000005995 Aluminium silicate Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- -1 aliphatic diamines Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- YZYDPPZYDIRSJT-UHFFFAOYSA-K boron phosphate Chemical compound [B+3].[O-]P([O-])([O-])=O YZYDPPZYDIRSJT-UHFFFAOYSA-K 0.000 description 1
- 229910000149 boron phosphate Inorganic materials 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical compound O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Catalysts (AREA)
- Hydrogenated Pyridines (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE553813A true BE553813A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Family
ID=178473
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE553813D BE553813A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE553813A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) |
-
0
- BE BE553813D patent/BE553813A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5302756A (en) | Ammonolysis of nylon | |
EP2365964B1 (fr) | Procede de fabrication de composes comprenant des fonctions nitriles | |
WO2020183105A1 (fr) | Procédé de synthèse d'oligomères d'acide acrylique | |
FR2489322A1 (fr) | Procede de preparation de n-(alkylaminoalkyl) acrylamides | |
BE553813A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
FR2459285A1 (fr) | Procede microbiologique pour la production d'une solution aqueuse d'acrylamide fortement concentree | |
DK155880B (da) | Omega-formylalkansyre og fremgangsmaade til fremstilling deraf | |
BE553812A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
FR2485002A1 (fr) | Procede de purification d'une solution aqueuse d'acrylamide en vue de sa polymerisation | |
CH265193A (fr) | Procédé pour la production de B-diméthyl-aminopropionitrile. | |
FR2470761A1 (fr) | Procede de preparation de l'acide trimellitique | |
BE891203R (fr) | Procede d'oxyacetylation catalysee par le palladium de l'acetate de phenyle en acetoxyacetophenones | |
BE483465A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
HU187285B (en) | Process for producing nitrils | |
BE522755A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
TW200415145A (en) | Process for the preparation of ε-caprolactam from a mixture comprising 6-aminocaproamide and/or oligomers | |
BE427098A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
CH439269A (fr) | Procédé de préparation d'une cycloalcanone | |
BE439987A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
BE891910A (fr) | Procede de preparation continue du dichloro-1,2 ethane | |
CH385879A (fr) | Procédé de fabrication de l'éthylènediamine | |
BE436763A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
CH237384A (fr) | Procédé de préparation d'acétonitrile. | |
BE571002A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
FR2463126A1 (fr) | Procede de production de 2-pyrrolidone |