BE574349A - - Google Patents
Info
- Publication number
- BE574349A BE574349A BE574349DA BE574349A BE 574349 A BE574349 A BE 574349A BE 574349D A BE574349D A BE 574349DA BE 574349 A BE574349 A BE 574349A
- Authority
- BE
- Belgium
- Prior art keywords
- adiponitrile
- sep
- nitric acid
- acid
- treating
- Prior art date
Links
- BTGRAWJCKBQKAO-UHFFFAOYSA-N Adiponitrile Chemical compound N#CCCCCC#N BTGRAWJCKBQKAO-UHFFFAOYSA-N 0.000 claims description 90
- GRYLNZFGIOXLOG-UHFFFAOYSA-N nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 62
- 150000002825 nitriles Chemical class 0.000 claims description 31
- 238000000034 method Methods 0.000 claims description 29
- 239000012535 impurity Substances 0.000 claims description 28
- 238000004821 distillation Methods 0.000 claims description 18
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 239000002253 acid Substances 0.000 claims description 13
- -1 aliphatic nitriles Chemical class 0.000 claims description 13
- 238000000746 purification Methods 0.000 claims description 13
- 238000005406 washing Methods 0.000 claims description 11
- 235000011121 sodium hydroxide Nutrition 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 238000011084 recovery Methods 0.000 claims description 2
- 239000000243 solution Substances 0.000 claims 3
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims 2
- 239000007864 aqueous solution Substances 0.000 claims 2
- 238000000926 separation method Methods 0.000 claims 1
- 229920001098 polystyrene-block-poly(ethylene/propylene) Polymers 0.000 description 193
- VZJVWSHVAAUDKD-UHFFFAOYSA-N Potassium permanganate Chemical compound [K+].[O-][Mn](=O)(=O)=O VZJVWSHVAAUDKD-UHFFFAOYSA-N 0.000 description 55
- NAQMVNRVTILPCV-UHFFFAOYSA-N Hexamethylenediamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 11
- WNLRTRBMVRJNCN-UHFFFAOYSA-N Adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 8
- 239000004677 Nylon Substances 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 229920001778 nylon Polymers 0.000 description 8
- 230000005484 gravity Effects 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000003513 alkali Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000001361 adipic acid Substances 0.000 description 4
- 235000011037 adipic acid Nutrition 0.000 description 4
- 239000003518 caustics Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000004448 titration Methods 0.000 description 4
- NLKNQRATVPKPDG-UHFFFAOYSA-M Potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 238000009434 installation Methods 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- KVNRLNFWIYMESJ-UHFFFAOYSA-N Butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 2
- ZTOMUSMDRMJOTH-UHFFFAOYSA-N Glutaronitrile Chemical compound N#CCCCC#N ZTOMUSMDRMJOTH-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 125000004432 carbon atoms Chemical group C* 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- DFJYZCUIKPGCSG-UHFFFAOYSA-N decanedinitrile Chemical compound N#CCCCCCCCCC#N DFJYZCUIKPGCSG-UHFFFAOYSA-N 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 238000007710 freezing Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- 241001550224 Apha Species 0.000 description 1
- BGTOWKSIORTVQH-UHFFFAOYSA-N Cyclopentanone Chemical class O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 1
- CUONGYYJJVDODC-UHFFFAOYSA-N Malononitrile Chemical compound N#CCC#N CUONGYYJJVDODC-UHFFFAOYSA-N 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N Propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L Sodium thiosulphate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- IAHFWCOBPZCAEA-UHFFFAOYSA-N Succinonitrile Chemical compound N#CCCC#N IAHFWCOBPZCAEA-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910052803 cobalt Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000005712 crystallization Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- VXCUURYYWGCLIH-UHFFFAOYSA-N dodecanenitrile Chemical compound CCCCCCCCCCCC#N VXCUURYYWGCLIH-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- AILKHAQXUAOOFU-UHFFFAOYSA-N hexanenitrile Chemical compound CCCCCC#N AILKHAQXUAOOFU-UHFFFAOYSA-N 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- RHSBIGNQEIPSCT-UHFFFAOYSA-N octadecanenitrile Chemical compound CCCCCCCCCCCCCCCCCC#N RHSBIGNQEIPSCT-UHFFFAOYSA-N 0.000 description 1
- YSIMAPNUZAVQER-UHFFFAOYSA-N octanenitrile Chemical compound CCCCCCCC#N YSIMAPNUZAVQER-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- 239000002351 wastewater 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE574349A true BE574349A (ru) |
Family
ID=190739
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE574349D BE574349A (ru) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE574349A (ru) |
-
0
- BE BE574349D patent/BE574349A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
FR2501673A1 (fr) | Procede continu de production d'acide terephtalique | |
FR2478627A1 (fr) | Procede de production et de recuperation d'acide terephtalique | |
EP2443082A1 (fr) | Procede de production de cristaux d'acide adipique. | |
BE574349A (ru) | ||
EP0121466B1 (fr) | Procédé de décomposition d'un complexe d'acide orthobenzoyl-benzoique, de fluorure d'hydrogène et de trifluorure de bore | |
JP2500977B2 (ja) | シクロヘキサノンの製造方法 | |
WO1997000714A1 (fr) | Procede de purification par extraction d'un milieu liquide | |
FR2619563A1 (fr) | Procede avec recyclage d'acide use pour la production d'acide ou esters methacryliques | |
US2920099A (en) | Purification of aliphatic nitriles | |
FR2467842A1 (fr) | Procede pour la production d'iminodiacetonitrile | |
FR2607808A1 (fr) | Procede de preparation de trifluoromethylbenzonitrile a partir de trifluoromethylbenzaldehyde | |
JP2713014B2 (ja) | カプロラクタムの製法 | |
EP0000464A1 (fr) | Procédé de purification du mercaptobenzothiazole | |
CH405291A (fr) | Procédé de fabrication de cyclohexanone-oxime | |
BE738124A (en) | Prod of propylene oxide from propylene chlorobydrin | |
BE498029A (ru) | ||
CH372651A (fr) | Procédé de préparation d'acides mono- et dicarboxyliques | |
JP2002284736A (ja) | 無水酢酸の製造法 | |
FR2588859A1 (fr) | Procede pour la production du di(hydroxy-2 propyl-2)-2,6 naphtalene | |
BE491627A (ru) | ||
KR100311914B1 (ko) | 저순도카프로락탐의정제방법 | |
BE578748A (ru) | ||
FR2774374A1 (fr) | Procede pour la production de terephtalate d'un metal alcalin purifie, issu de produits de saponification de polyterephtalates d'alkylene de recuperation | |
BE623182A (ru) | ||
BE529588A (ru) |