DE1595302A1 - Verfahren zur Herstellung von wasserloeslichen Kondensationsprodukten - Google Patents
Verfahren zur Herstellung von wasserloeslichen KondensationsproduktenInfo
- Publication number
 - DE1595302A1 DE1595302A1 DE19661595302 DE1595302A DE1595302A1 DE 1595302 A1 DE1595302 A1 DE 1595302A1 DE 19661595302 DE19661595302 DE 19661595302 DE 1595302 A DE1595302 A DE 1595302A DE 1595302 A1 DE1595302 A1 DE 1595302A1
 - Authority
 - DE
 - Germany
 - Prior art keywords
 - water
 - mole
 - reaction
 - alkylenepolyamine
 - process according
 - Prior art date
 - Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
 - Pending
 
Links
- 239000007859 condensation product Substances 0.000 title claims description 13
 - 238000000034 method Methods 0.000 title claims description 11
 - 238000004519 manufacturing process Methods 0.000 title 1
 - 238000006243 chemical reaction Methods 0.000 claims description 10
 - BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 9
 - XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
 - 229920000768 polyamine Polymers 0.000 claims description 8
 - 239000007864 aqueous solution Substances 0.000 claims description 7
 - 239000000243 solution Substances 0.000 claims description 7
 - 125000002947 alkylene group Chemical group 0.000 claims description 6
 - 239000003795 chemical substances by application Substances 0.000 claims description 6
 - 125000003277 amino group Chemical group 0.000 claims description 5
 - 239000002253 acid Substances 0.000 claims description 4
 - 125000004432 carbon atom Chemical group C* 0.000 claims description 4
 - 238000002360 preparation method Methods 0.000 claims description 4
 - 239000011541 reaction mixture Substances 0.000 claims description 4
 - JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims description 3
 - RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 2
 - 239000012736 aqueous medium Substances 0.000 claims description 2
 - 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
 - 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
 - VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
 - 238000009833 condensation Methods 0.000 description 5
 - 230000005494 condensation Effects 0.000 description 5
 - 239000000047 product Substances 0.000 description 5
 - 239000004753 textile Substances 0.000 description 4
 - QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
 - -1 1,3-propylene Chemical group 0.000 description 2
 - QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
 - IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
 - QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
 - 239000002585 base Substances 0.000 description 2
 - 150000001875 compounds Chemical class 0.000 description 2
 - 238000010438 heat treatment Methods 0.000 description 2
 - NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
 - UYBWIEGTWASWSR-UHFFFAOYSA-N 1,3-diaminopropan-2-ol Chemical compound NCC(O)CN UYBWIEGTWASWSR-UHFFFAOYSA-N 0.000 description 1
 - VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
 - LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
 - PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
 - 101100383370 Squalus acanthias CFTR gene Proteins 0.000 description 1
 - 150000007513 acids Chemical class 0.000 description 1
 - 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
 - 150000008041 alkali metal carbonates Chemical class 0.000 description 1
 - 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
 - 150000001412 amines Chemical class 0.000 description 1
 - 229910021529 ammonia Inorganic materials 0.000 description 1
 - 238000004873 anchoring Methods 0.000 description 1
 - 239000007795 chemical reaction product Substances 0.000 description 1
 - 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
 - 238000002845 discoloration Methods 0.000 description 1
 - 238000004821 distillation Methods 0.000 description 1
 - 230000000694 effects Effects 0.000 description 1
 - 230000008030 elimination Effects 0.000 description 1
 - 238000003379 elimination reaction Methods 0.000 description 1
 - 238000005516 engineering process Methods 0.000 description 1
 - 239000000945 filler Substances 0.000 description 1
 - 239000000834 fixative Substances 0.000 description 1
 - 239000008394 flocculating agent Substances 0.000 description 1
 - 230000014759 maintenance of location Effects 0.000 description 1
 - 239000000463 material Substances 0.000 description 1
 - 239000002609 medium Substances 0.000 description 1
 - 239000000203 mixture Substances 0.000 description 1
 - LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 description 1
 - 229910052757 nitrogen Inorganic materials 0.000 description 1
 - 239000012299 nitrogen atmosphere Substances 0.000 description 1
 - 239000000123 paper Substances 0.000 description 1
 - 239000002985 plastic film Substances 0.000 description 1
 - 229920006255 plastic film Polymers 0.000 description 1
 - 238000003918 potentiometric titration Methods 0.000 description 1
 - 230000035484 reaction time Effects 0.000 description 1
 - 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
 - 239000007858 starting material Substances 0.000 description 1
 - 238000009988 textile finishing Methods 0.000 description 1
 - 230000007704 transition Effects 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
 - C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
 - C08G73/02—Polyamines
 - C08G73/0206—Polyalkylene(poly)amines
 - C08G73/0213—Preparatory process
 - C08G73/022—Preparatory process from polyamines and epihalohydrins
 
 
Landscapes
- Chemical & Material Sciences (AREA)
 - Health & Medical Sciences (AREA)
 - Chemical Kinetics & Catalysis (AREA)
 - Medicinal Chemistry (AREA)
 - Polymers & Plastics (AREA)
 - Organic Chemistry (AREA)
 - Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
 - Polyamides (AREA)
 - Paper (AREA)
 
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| DEB0085704 | 1966-02-08 | 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| DE1595302A1 true DE1595302A1 (de) | 1970-03-05 | 
Family
ID=6983032
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| DE19661595302 Pending DE1595302A1 (de) | 1966-02-08 | 1966-02-08 | Verfahren zur Herstellung von wasserloeslichen Kondensationsprodukten | 
Country Status (8)
| Country | Link | 
|---|---|
| AT (1) | AT267870B (forum.php) | 
| BE (1) | BE693442A (forum.php) | 
| CH (1) | CH495385A (forum.php) | 
| DE (1) | DE1595302A1 (forum.php) | 
| FR (1) | FR1510556A (forum.php) | 
| GB (1) | GB1165394A (forum.php) | 
| NL (1) | NL6701449A (forum.php) | 
| SE (1) | SE305082B (forum.php) | 
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| DE3300866A1 (de) * | 1983-01-13 | 1984-07-19 | Basf Ag, 6700 Ludwigshafen | Oxalkylierte polyamidoamine, deren herstellung und deren verwendung als erdoelemulsionsspalter | 
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| DE2756469A1 (de) * | 1977-12-17 | 1979-06-21 | Bayer Ag | Amidgruppenhaltige polyamine | 
| DE3810424A1 (de) * | 1988-03-26 | 1989-10-12 | Bayer Ag | Stickstoffhaltige polymere verbindungen | 
- 
        1966
        
- 1966-02-08 DE DE19661595302 patent/DE1595302A1/de active Pending
 
 - 
        1967
        
- 1967-01-30 NL NL6701449A patent/NL6701449A/xx unknown
 - 1967-01-31 CH CH142767A patent/CH495385A/de not_active IP Right Cessation
 - 1967-01-31 BE BE693442D patent/BE693442A/xx unknown
 - 1967-02-07 FR FR93989A patent/FR1510556A/fr not_active Expired
 - 1967-02-07 GB GB579067A patent/GB1165394A/en not_active Expired
 - 1967-02-08 AT AT120867A patent/AT267870B/de active
 - 1967-02-08 SE SE1783/67A patent/SE305082B/xx unknown
 
 
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| DE3300866A1 (de) * | 1983-01-13 | 1984-07-19 | Basf Ag, 6700 Ludwigshafen | Oxalkylierte polyamidoamine, deren herstellung und deren verwendung als erdoelemulsionsspalter | 
Also Published As
| Publication number | Publication date | 
|---|---|
| SE305082B (forum.php) | 1968-10-14 | 
| GB1165394A (en) | 1969-09-24 | 
| FR1510556A (fr) | 1968-01-19 | 
| BE693442A (forum.php) | 1967-07-31 | 
| AT267870B (de) | 1969-01-27 | 
| NL6701449A (forum.php) | 1967-08-09 | 
| CH495385A (de) | 1970-08-31 | 
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