PT1475367E - ¿processo para destilação de uma mistura de isómeros de diisocianato de difenilmetano - Google Patents
¿processo para destilação de uma mistura de isómeros de diisocianato de difenilmetano Download PDFInfo
- Publication number
- PT1475367E PT1475367E PT04009786T PT04009786T PT1475367E PT 1475367 E PT1475367 E PT 1475367E PT 04009786 T PT04009786 T PT 04009786T PT 04009786 T PT04009786 T PT 04009786T PT 1475367 E PT1475367 E PT 1475367E
- Authority
- PT
- Portugal
- Prior art keywords
- mdi
- distillation
- column
- diphenylmethane
- diisocyanate
- Prior art date
Links
- 238000004821 distillation Methods 0.000 title claims abstract description 85
- LNWBFIVSTXCJJG-UHFFFAOYSA-N [diisocyanato(phenyl)methyl]benzene Chemical class C=1C=CC=CC=1C(N=C=O)(N=C=O)C1=CC=CC=C1 LNWBFIVSTXCJJG-UHFFFAOYSA-N 0.000 title 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims abstract description 79
- 239000000203 mixture Substances 0.000 claims abstract description 48
- LFSYUSUFCBOHGU-UHFFFAOYSA-N 1-isocyanato-2-[(4-isocyanatophenyl)methyl]benzene Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=CC=C1N=C=O LFSYUSUFCBOHGU-UHFFFAOYSA-N 0.000 claims abstract description 15
- JIABEENURMZTTI-UHFFFAOYSA-N 1-isocyanato-2-[(2-isocyanatophenyl)methyl]benzene Chemical compound O=C=NC1=CC=CC=C1CC1=CC=CC=C1N=C=O JIABEENURMZTTI-UHFFFAOYSA-N 0.000 claims abstract description 10
- 238000000926 separation method Methods 0.000 claims description 81
- 238000000034 method Methods 0.000 claims description 36
- 238000005194 fractionation Methods 0.000 description 34
- 239000000047 product Substances 0.000 description 25
- 238000000605 extraction Methods 0.000 description 13
- 239000000126 substance Substances 0.000 description 10
- 238000010992 reflux Methods 0.000 description 9
- 239000000463 material Substances 0.000 description 7
- 238000005192 partition Methods 0.000 description 6
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 5
- 239000012535 impurity Substances 0.000 description 5
- 229920001228 polyisocyanate Polymers 0.000 description 5
- 239000005056 polyisocyanate Substances 0.000 description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000005265 energy consumption Methods 0.000 description 3
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 2
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 2
- AWGBKZRMLNVLAF-UHFFFAOYSA-N 3,5-dibromo-n,2-dihydroxybenzamide Chemical compound ONC(=O)C1=CC(Br)=CC(Br)=C1O AWGBKZRMLNVLAF-UHFFFAOYSA-N 0.000 description 1
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-diisopropylethylamine Substances CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 1
- OUCPJZWNFRYRBI-UHFFFAOYSA-N aniline;formaldehyde Chemical compound O=C.NC1=CC=CC=C1 OUCPJZWNFRYRBI-UHFFFAOYSA-N 0.000 description 1
- ZPHQBFRCXUIIAZ-UHFFFAOYSA-N benzene;hydrochloride Chemical compound Cl.C1=CC=CC=C1 ZPHQBFRCXUIIAZ-UHFFFAOYSA-N 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000007781 pre-processing Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C263/00—Preparation of derivatives of isocyanic acid
- C07C263/18—Separation; Purification; Stabilisation; Use of additives
- C07C263/20—Separation; Purification
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10320504 | 2003-05-08 | ||
| DE102004001872A DE102004001872A1 (de) | 2003-05-08 | 2004-01-14 | Verfahren zur Destillation eines Gemisches isomerer Diisocyanatodiphenylmethane |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PT1475367E true PT1475367E (pt) | 2010-09-06 |
Family
ID=33440660
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PT04009786T PT1475367E (pt) | 2003-05-08 | 2004-04-24 | ¿processo para destilação de uma mistura de isómeros de diisocianato de difenilmetano |
Country Status (5)
| Country | Link |
|---|---|
| AT (1) | ATE473207T1 (de) |
| DE (2) | DE102004001872A1 (de) |
| ES (1) | ES2346873T3 (de) |
| PT (1) | PT1475367E (de) |
| TW (1) | TW200505827A (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3687650A1 (de) * | 2017-09-28 | 2020-08-05 | ExxonMobil Research and Engineering Company | Doppelte trennwandsäule mit mehreren produkten |
-
2004
- 2004-01-14 DE DE102004001872A patent/DE102004001872A1/de not_active Withdrawn
- 2004-04-24 ES ES04009786T patent/ES2346873T3/es not_active Expired - Lifetime
- 2004-04-24 PT PT04009786T patent/PT1475367E/pt unknown
- 2004-04-24 AT AT04009786T patent/ATE473207T1/de active
- 2004-04-24 DE DE502004011353T patent/DE502004011353D1/de not_active Expired - Lifetime
- 2004-05-07 TW TW093112837A patent/TW200505827A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ATE473207T1 (de) | 2010-07-15 |
| TW200505827A (en) | 2005-02-16 |
| ES2346873T3 (es) | 2010-10-21 |
| DE102004001872A1 (de) | 2004-12-09 |
| DE502004011353D1 (de) | 2010-08-19 |
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