FI61707C - Foerfarande foer framstaellning av kvaevehaltiga kondensationsprodukter fraon polyalkylenpolyaminer och polyalkylenoxidderivat - Google Patents
Foerfarande foer framstaellning av kvaevehaltiga kondensationsprodukter fraon polyalkylenpolyaminer och polyalkylenoxidderivat Download PDFInfo
- Publication number
- FI61707C FI61707C FI752041A FI752041A FI61707C FI 61707 C FI61707 C FI 61707C FI 752041 A FI752041 A FI 752041A FI 752041 A FI752041 A FI 752041A FI 61707 C FI61707 C FI 61707C
- Authority
- FI
- Finland
- Prior art keywords
- additive
- paper
- resin
- filler
- cellulose
- Prior art date
Links
- 229920000768 polyamine Polymers 0.000 abstract description 19
- 229920001281 polyalkylene Polymers 0.000 abstract description 17
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract description 15
- 229920000233 poly(alkylene oxides) Polymers 0.000 abstract description 9
- 239000007864 aqueous solution Substances 0.000 abstract description 6
- 125000002947 alkylene group Chemical group 0.000 abstract description 5
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 239000007795 chemical reaction product Substances 0.000 abstract description 2
- 239000000654 additive Substances 0.000 description 103
- 230000000996 additive effect Effects 0.000 description 101
- 239000011347 resin Substances 0.000 description 60
- 229920005989 resin Polymers 0.000 description 60
- 239000000945 filler Substances 0.000 description 57
- 239000001913 cellulose Substances 0.000 description 53
- 229920002678 cellulose Polymers 0.000 description 53
- 230000000694 effects Effects 0.000 description 45
- 229920002873 Polyethylenimine Polymers 0.000 description 37
- 229940037003 alum Drugs 0.000 description 35
- 230000014759 maintenance of location Effects 0.000 description 28
- 239000000835 fiber Substances 0.000 description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 25
- 230000001133 acceleration Effects 0.000 description 20
- 238000000227 grinding Methods 0.000 description 19
- 230000003287 optical effect Effects 0.000 description 19
- 238000006243 chemical reaction Methods 0.000 description 18
- 239000000047 product Substances 0.000 description 18
- 239000000725 suspension Substances 0.000 description 17
- 238000000034 method Methods 0.000 description 12
- 238000004132 cross linking Methods 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 239000003431 cross linking reagent Substances 0.000 description 9
- 230000008569 process Effects 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 230000002378 acidificating effect Effects 0.000 description 6
- 230000007935 neutral effect Effects 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 5
- 239000007859 condensation product Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000546 pharmaceutical excipient Substances 0.000 description 4
- 229920000962 poly(amidoamine) Polymers 0.000 description 4
- -1 1,2-propylene Chemical group 0.000 description 3
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 239000002841 Lewis acid Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 238000012512 characterization method Methods 0.000 description 3
- 150000007517 lewis acids Chemical class 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 241001223352 Rissa Species 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical group CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 125000001033 ether group Chemical group 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 230000001976 improved effect Effects 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 1
- BNZCDZDLTIHJAC-UHFFFAOYSA-N 2-azaniumylethylazanium;sulfate Chemical compound NCC[NH3+].OS([O-])(=O)=O BNZCDZDLTIHJAC-UHFFFAOYSA-N 0.000 description 1
- KPICIOOAGPZSKI-UHFFFAOYSA-N 2-benzyl-4-nitropyridine Chemical compound [O-][N+](=O)C1=CC=NC(CC=2C=CC=CC=2)=C1 KPICIOOAGPZSKI-UHFFFAOYSA-N 0.000 description 1
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 102220628222 Coagulation factor IX_R46T_mutation Human genes 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 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 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 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
- 230000006855 networking Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 229920000333 poly(propyleneimine) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001451 polypropylene glycol Chemical group 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 238000005956 quaternization reaction Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
- C02F1/54—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using organic material
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
- C08G65/2606—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups
- C08G65/2609—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups containing aliphatic hydroxyl groups
-
- 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
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/54—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/06—Paper forming aids
- D21H21/10—Retention agents or drainage improvers
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Water Supply & Treatment (AREA)
- Environmental & Geological Engineering (AREA)
- Hydrology & Water Resources (AREA)
- Life Sciences & Earth Sciences (AREA)
- Paper (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Glass Compositions (AREA)
- Auxiliary Devices For And Details Of Packaging Control (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2436386 | 1974-07-29 | ||
| DE2436386A DE2436386C2 (de) | 1974-07-29 | 1974-07-29 | Verwendung stickstoffhaltiger Kondensationsprodukte |
| US05/594,648 US4066494A (en) | 1974-07-29 | 1975-07-10 | Nitrogenous condensation products used as retention aids in papermaking |
| US59464875 | 1975-07-10 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI752041A FI752041A (no) | 1976-01-30 |
| FI61707B FI61707B (fi) | 1982-05-31 |
| FI61707C true FI61707C (fi) | 1982-09-10 |
Family
ID=35266732
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI752041A FI61707C (fi) | 1974-07-29 | 1975-07-15 | Foerfarande foer framstaellning av kvaevehaltiga kondensationsprodukter fraon polyalkylenpolyaminer och polyalkylenoxidderivat |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4066494A (no) |
| JP (2) | JPS5836002B2 (no) |
| BE (1) | BE831757A (no) |
| CA (1) | CA1063276A (no) |
| CH (1) | CH597279A5 (no) |
| DE (1) | DE2436386C2 (no) |
| FI (1) | FI61707C (no) |
| FR (1) | FR2280670A1 (no) |
| GB (1) | GB1506885A (no) |
| NL (1) | NL181203C (no) |
| NO (1) | NO143429C (no) |
| SE (1) | SE450959B (no) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2733973A1 (de) * | 1977-07-28 | 1979-02-15 | Basf Ag | Wasserloesliche, vernetzte stickstoffhaltige kondensationsprodukte |
| US4210488A (en) * | 1977-10-13 | 1980-07-01 | Reuss Peter J | Process for improving the dry strength of paper and for improving the effect of optical brighteners in the preparation or coating of paper |
| US4347339A (en) * | 1981-05-08 | 1982-08-31 | Nalco Chemical Company | Cationic block copolymers |
| US4689374A (en) * | 1983-06-09 | 1987-08-25 | W. R. Grace & Co. | Water soluble polyamidoaminepolyamine having weight average molecular weight of at least 5×105 |
| DE3347257A1 (de) * | 1983-12-28 | 1985-07-11 | Basf Ag, 6700 Ludwigshafen | Vernetzte oxalkylierte polyalkylenpolyamine und ihre verwendung als erdoelemulsionsspalter |
| DE3413567A1 (de) * | 1984-04-11 | 1985-10-24 | Bayer Ag, 5090 Leverkusen | Papierhilfsmittel |
| US5223097A (en) * | 1986-01-09 | 1993-06-29 | W. R. Grace Ab | Method for controlling pitch on a paper-making machine |
| US5626720A (en) * | 1986-01-09 | 1997-05-06 | W.R. Grace & Co.-Conn. | Method for controlling pitch on a papermaking machine |
| JPH0613606B1 (no) * | 1987-06-22 | 1994-02-23 | Nippon Catalytic Chem Ind | |
| WO1988010277A1 (en) * | 1987-06-22 | 1988-12-29 | Nippon Shokubai Kagaku Kogyo Kabushiki Kaisha | Process for preparing cationic, water-soluble resin and water-treating agent containing said resin |
| JPH02145372U (no) * | 1989-05-15 | 1990-12-10 | ||
| DE4240110A1 (de) * | 1992-11-28 | 1994-06-01 | Basf Ag | Kondensationsprodukte von Polyalkylenpolyaminen, Verfahren zu ihrer Herstellung und ihre Verwendung bei der Herstellung von Papier |
| DE4244194A1 (de) * | 1992-12-24 | 1994-06-30 | Basf Ag | Wasserlösliche Kondensationsprodukte aus Aminogruppen enthaltenden Verbindungen und Vernetzern, Verfahren zu ihrer Herstellung und ihre Verwendung |
| AU711553B2 (en) * | 1996-01-08 | 1999-10-14 | Basf Aktiengesellschaft | Process for the preparation of water-soluble amino-containing condensates and adducts and their use |
| DE19921507A1 (de) | 1999-05-10 | 2000-11-16 | Basf Ag | Verfahren zur Fraktionierung von in Wasser löslichen oder dispergierbaren aminogruppenhaltigen Polymeren mit breiter Molmassenverteilung |
| US6673205B2 (en) | 2001-05-10 | 2004-01-06 | Fort James Corporation | Use of hydrophobically modified polyaminamides with polyethylene glycol esters in paper products |
| US7041197B2 (en) * | 2003-04-15 | 2006-05-09 | Fort James Corporation | Wet strength and softness enhancement of paper products |
| DE102004025861A1 (de) | 2004-05-24 | 2005-12-22 | Basf Ag | Verfahren zur Herstellung von gekrepptem Papier |
| WO2010020551A1 (de) * | 2008-08-18 | 2010-02-25 | Basf Se | Verfahren zur erhöhung der trockenfestigkeit von papier, pappe und karton |
| DE102010026490A1 (de) | 2010-07-07 | 2012-01-12 | Basf Se | Verfahren zur Herstellung von feinstrukturierten Oberflächen |
| WO2016096477A1 (de) | 2014-12-16 | 2016-06-23 | Basf Se | Verfahren zur herstellung von papier und karton |
| EP3173449A1 (de) | 2015-11-27 | 2017-05-31 | BASF Coatings GmbH | Verbund aus zwei festkörpern |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA686202A (en) * | 1964-05-12 | E. Eddy Roderick | Process for improving the dye retention characteristics of cellulosic materials | |
| NL109055C (no) * | 1955-06-28 | |||
| IT626236A (no) * | 1959-01-16 | Boehme Chemie Gmbh | ||
| US3251852A (en) * | 1959-06-15 | 1966-05-17 | Petrolite Corp | Amino polymers |
| US3129133A (en) * | 1960-04-21 | 1964-04-14 | Shell Oil Co | Colloidal dispersions of partially cured polyepoxides, their preparation and use for preparing wet strength paper |
| NL300100A (no) * | 1962-11-05 | |||
| FR1374669A (fr) * | 1962-11-05 | 1964-10-09 | Dow Chemical Co | Agents de floculation polymères |
| DE1570296B2 (de) * | 1965-09-02 | 1970-10-29 | Badische Anilin- S Soda-Fabrik AO, 6700 Ludwigshafen | Verfahren zur Herstellung wasserlöslicher Derivate von Polyalkyleniminen |
| DE1546290A1 (de) * | 1966-04-30 | 1970-02-26 | Bayer Ag | Flotationsmittel fuer die Faser- und Fuellstoffrueckgewinnung aus Papiermaschinenabwaessern |
| US3635842A (en) * | 1966-06-27 | 1972-01-18 | Dow Chemical Co | Short life paper size from modified polyalkylene-imines |
| DE2042453A1 (en) * | 1970-08-27 | 1972-03-02 | Rotta Chem Fab Theodor | Condensates of reaction products of alkylene polyamines - with epichlorohydrine, and chlorohydrin ethers of polyalkylene glycol |
| US3746678A (en) * | 1971-09-13 | 1973-07-17 | Dow Chemical Co | Amine-modified polyalkylene oxides |
-
1974
- 1974-07-29 DE DE2436386A patent/DE2436386C2/de not_active Expired
-
1975
- 1975-07-10 US US05/594,648 patent/US4066494A/en not_active Expired - Lifetime
- 1975-07-11 CA CA231,430A patent/CA1063276A/en not_active Expired
- 1975-07-15 FI FI752041A patent/FI61707C/fi not_active IP Right Cessation
- 1975-07-22 NO NO752597A patent/NO143429C/no unknown
- 1975-07-23 SE SE7508400A patent/SE450959B/xx not_active IP Right Cessation
- 1975-07-23 FR FR7522992A patent/FR2280670A1/fr active Granted
- 1975-07-25 BE BE158632A patent/BE831757A/xx not_active IP Right Cessation
- 1975-07-25 CH CH975175A patent/CH597279A5/xx not_active IP Right Cessation
- 1975-07-28 GB GB31446/75A patent/GB1506885A/en not_active Expired
- 1975-07-29 NL NLAANVRAGE7509040,A patent/NL181203C/xx not_active IP Right Cessation
- 1975-07-29 JP JP50091625A patent/JPS5836002B2/ja not_active Expired
-
1983
- 1983-04-05 JP JP58058805A patent/JPS58197399A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| SE7508400L (sv) | 1976-01-30 |
| NL181203B (nl) | 1987-02-02 |
| NO752597L (no) | 1976-01-30 |
| NL7509040A (nl) | 1976-02-02 |
| FR2280670A1 (fr) | 1976-02-27 |
| FI752041A (no) | 1976-01-30 |
| NO143429B (no) | 1980-11-03 |
| JPS58197399A (ja) | 1983-11-17 |
| CA1063276A (en) | 1979-09-25 |
| SE450959B (sv) | 1987-08-17 |
| US4066494A (en) | 1978-01-03 |
| JPS6244080B2 (no) | 1987-09-18 |
| FI61707B (fi) | 1982-05-31 |
| DE2436386A1 (de) | 1976-02-12 |
| BE831757A (fr) | 1976-01-26 |
| DE2436386C2 (de) | 1982-09-23 |
| NL181203C (nl) | 1987-07-01 |
| NO143429C (no) | 1981-02-11 |
| GB1506885A (en) | 1978-04-12 |
| AU8296775A (en) | 1977-01-13 |
| FR2280670B1 (no) | 1978-07-28 |
| CH597279A5 (no) | 1978-03-31 |
| JPS5137200A (no) | 1976-03-29 |
| JPS5836002B2 (ja) | 1983-08-06 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: BASF AKTIENGESELLSCHAFT |