BE626553A - - Google Patents
Info
- Publication number
- BE626553A BE626553A BE626553DA BE626553A BE 626553 A BE626553 A BE 626553A BE 626553D A BE626553D A BE 626553DA BE 626553 A BE626553 A BE 626553A
- Authority
- BE
- Belgium
- Prior art keywords
- ester
- pure
- carbamic
- alcohol
- water
- Prior art date
Links
- 150000002148 esters Chemical class 0.000 claims description 30
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 14
- 239000000243 solution Substances 0.000 claims description 13
- 239000007864 aqueous solution Substances 0.000 claims description 12
- 230000015572 biosynthetic process Effects 0.000 claims description 11
- 239000012535 impurity Substances 0.000 claims description 11
- 238000003786 synthesis reaction Methods 0.000 claims description 11
- 238000002425 crystallisation Methods 0.000 claims description 9
- 230000008025 crystallization Effects 0.000 claims description 9
- 238000000926 separation method Methods 0.000 claims description 8
- 230000001476 alcoholic effect Effects 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
- 239000004202 carbamide Substances 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 4
- 238000004821 distillation Methods 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 239000013078 crystal Substances 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 210000000709 aorta Anatomy 0.000 claims 1
- 238000010924 continuous production Methods 0.000 claims 1
- 230000003247 decreasing effect Effects 0.000 claims 1
- 239000012527 feed solution Substances 0.000 claims 1
- XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 claims 1
- 235000019441 ethanol Nutrition 0.000 description 15
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 229910002651 NO3 Inorganic materials 0.000 description 4
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 3
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical group [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000007872 degassing Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 101100395869 Escherichia coli sta3 gene Proteins 0.000 description 1
- 241001599630 Stelis <bee> Species 0.000 description 1
- PRORZGWHZXZQMV-UHFFFAOYSA-N azane;nitric acid Chemical compound N.O[N+]([O-])=O PRORZGWHZXZQMV-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- -1 carbon ester Chemical class 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE626553A true BE626553A (enrdf_load_stackoverflow) |
Family
ID=197294
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE626553D BE626553A (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE626553A (enrdf_load_stackoverflow) |
-
0
- BE BE626553D patent/BE626553A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CZ298267B6 (cs) | Zpusob prípravy kyseliny (meth)akrylové | |
JP2004359615A (ja) | アクリル酸の製造方法 | |
BE897039A (fr) | Procede de preparation d'ethylene glycol | |
JP2001199931A (ja) | アクリル酸の製造方法 | |
JP2000516949A (ja) | 尿素の製造法 | |
US4898990A (en) | Process for the extraction of vanillin | |
CN111470992A (zh) | 一种连续化合成甘氨酸的清洁工艺方法 | |
WO2008006977A1 (fr) | Procédé de préparation du 2-hydroxy-4-(méthylthio)butyronitrile et de la méthionine | |
US4254283A (en) | Process for preparing adipic acid with recovery of glutaric and succinic acids | |
US12110264B2 (en) | Process for producing urea and biuret | |
CA1217201A (en) | Process for synthesizing urea | |
CH405267A (fr) | Procédé d'extraction et de purification des esters carbamiques au cours de leur synthèse | |
BE626553A (enrdf_load_stackoverflow) | ||
US4207256A (en) | Treatment of water vapor generated in concentrating an aqueous urea solution | |
US3173961A (en) | Process for the separation of the products obtained through the nitration of cyclohexane in gaseous phase | |
CS228529B2 (en) | Process for the production of urea | |
JP3917201B2 (ja) | ビスフェノールaの製造方法 | |
US3232982A (en) | Urea synthesis | |
US20250197340A1 (en) | Method for preparation of high-purity (meth)acrylic acid | |
CN119735220A (zh) | 一种酮连氮制备过程产生的副产物碳酸铵的分离回收方法及装置 | |
JP4651175B2 (ja) | メタクリル酸の精製方法およびメタクリル酸メチルの製造方法 | |
KR20240031050A (ko) | 고순도 아크릴산의 제조방법 | |
FR2502973A1 (fr) | Procede pour separer, dans la fabrication industrielle de la melamine a partir de l'uree, des gouttelettes d'uree fondue et/ou d'un melange fondu d'uree et de ses produits de decomposition a la chaleur, d'un gaz residuaire deja debarrasse de la melamine | |
KR20240031056A (ko) | 고순도 아크릴산의 제조방법 | |
KR790001171B1 (ko) | 요소합성에 있어서의 미반응물 및 열의 회수법 |