SU460632A3 - Способ получени водорастворимых азотсодержащих полимеров - Google Patents
Способ получени водорастворимых азотсодержащих полимеровInfo
- Publication number
- SU460632A3 SU460632A3 SU1666628A SU1666628A SU460632A3 SU 460632 A3 SU460632 A3 SU 460632A3 SU 1666628 A SU1666628 A SU 1666628A SU 1666628 A SU1666628 A SU 1666628A SU 460632 A3 SU460632 A3 SU 460632A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- water
- reaction
- solution
- mol
- product
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 26
- 229920000642 polymer Polymers 0.000 title claims description 7
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 title claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 37
- 239000003431 cross linking reagent Substances 0.000 claims description 15
- 230000008569 process Effects 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 238000004132 cross linking Methods 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 5
- 229920000768 polyamine Polymers 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 125000004970 halomethyl group Chemical group 0.000 claims description 3
- 229920002755 poly(epichlorohydrin) Polymers 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 230000003311 flocculating effect Effects 0.000 claims 1
- 230000003472 neutralizing effect Effects 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 31
- 239000000243 solution Substances 0.000 description 31
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 239000000047 product Substances 0.000 description 15
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 14
- 239000000203 mixture Substances 0.000 description 14
- 239000013543 active substance Substances 0.000 description 13
- 239000007795 chemical reaction product Substances 0.000 description 12
- 150000001412 amines Chemical class 0.000 description 11
- 239000007864 aqueous solution Substances 0.000 description 11
- 238000001816 cooling Methods 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 10
- 239000011541 reaction mixture Substances 0.000 description 10
- 238000003756 stirring Methods 0.000 description 10
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 7
- -1 ether alcohols Chemical class 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 239000011780 sodium chloride Substances 0.000 description 7
- KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000014759 maintenance of location Effects 0.000 description 5
- 235000011121 sodium hydroxide Nutrition 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 229920000570 polyether Polymers 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical group NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
- 239000004721 Polyphenylene oxide Substances 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000012467 final product Substances 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
- 239000013067 intermediate product Substances 0.000 description 3
- 229920002521 macromolecule Polymers 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000009969 flowable effect Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Inorganic materials [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 230000000630 rising effect Effects 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- AGYUOJIYYGGHKV-UHFFFAOYSA-N 1,2-bis(2-chloroethoxy)ethane Chemical compound ClCCOCCOCCCl AGYUOJIYYGGHKV-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- GPTVQTPMFOLLOA-UHFFFAOYSA-N 1-chloro-2-ethoxyethane Chemical compound CCOCCCl GPTVQTPMFOLLOA-UHFFFAOYSA-N 0.000 description 1
- SEVIEHFDUHCSCV-UHFFFAOYSA-N 1-chlorobut-3-en-2-one Chemical group ClCC(=O)C=C SEVIEHFDUHCSCV-UHFFFAOYSA-N 0.000 description 1
- VUSYFNXNYLAECV-UHFFFAOYSA-N 2,3-bis(chloromethyl)oxirane Chemical compound ClCC1OC1CCl VUSYFNXNYLAECV-UHFFFAOYSA-N 0.000 description 1
- 125000006012 2-chloroethoxy group Chemical group 0.000 description 1
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241001414641 Polyamia Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- PWAXUOGZOSVGBO-UHFFFAOYSA-N adipoyl chloride Chemical compound ClC(=O)CCCCC(Cl)=O PWAXUOGZOSVGBO-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical compound C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000008396 flotation agent Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid group Chemical group C(\C=C/C(=O)O)(=O)O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012218 nanoagent Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 238000006053 organic reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L sodium sulphate Substances [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 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
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/53—Polyethers; Polyesters
-
- 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
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/36—Compounds containing oxirane rings with hydrocarbon radicals, substituted by nitrogen atoms
-
- 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
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/333—Polymers modified by chemical after-treatment with organic compounds containing nitrogen
- C08G65/33303—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing amino group
- C08G65/33306—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing amino group acyclic
-
- 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
- C08G73/024—Polyamines containing oxygen in the form of ether bonds in the main chain
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Water Supply & Treatment (AREA)
- Environmental & Geological Engineering (AREA)
- Engineering & Computer Science (AREA)
- Hydrology & Water Resources (AREA)
- Life Sciences & Earth Sciences (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Paper (AREA)
- Polyethers (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH845670A CH541595A (de) | 1970-06-05 | 1970-06-05 | Verfahren zur Herstellung von neuen Polyätheraminen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU460632A3 true SU460632A3 (ru) | 1975-02-15 |
Family
ID=4340645
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1666628A SU460632A3 (ru) | 1970-06-05 | 1971-06-03 | Способ получени водорастворимых азотсодержащих полимеров |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US3753931A (OSRAM) |
| JP (1) | JPS5229359B1 (OSRAM) |
| BE (1) | BE768202A (OSRAM) |
| CA (1) | CA922045A (OSRAM) |
| CH (1) | CH541595A (OSRAM) |
| DD (1) | DD97892A5 (OSRAM) |
| DE (1) | DE2127082C3 (OSRAM) |
| ES (1) | ES391897A1 (OSRAM) |
| FR (1) | FR2094084B1 (OSRAM) |
| GB (1) | GB1341058A (OSRAM) |
| HK (1) | HK80776A (OSRAM) |
| IT (1) | IT943404B (OSRAM) |
| NL (1) | NL146184B (OSRAM) |
| SE (2) | SE376622B (OSRAM) |
| SU (1) | SU460632A3 (OSRAM) |
| ZA (1) | ZA713624B (OSRAM) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4056510A (en) * | 1975-01-23 | 1977-11-01 | The Dow Chemical Company | Amine-modified polyethers |
| US4198269A (en) * | 1976-01-26 | 1980-04-15 | The Dow Chemical Company | Quaternary ammonium salts of epihalohydrin polymers as additives for fibrous cellulosic materials |
| DE2733973A1 (de) * | 1977-07-28 | 1979-02-15 | Basf Ag | Wasserloesliche, vernetzte stickstoffhaltige kondensationsprodukte |
| DE2736651A1 (de) * | 1977-08-13 | 1979-02-15 | Wolff Walsrode Ag | Hilfsmittel zur verbesserung der retention, entwaesserung und aufbereitung, insbesondere bei der papierherstellung |
| US4191820A (en) * | 1978-01-03 | 1980-03-04 | Basf Wyandotte Corporation | Process for preparing polyalkylene polyamine polyethers |
| US4178434A (en) * | 1978-01-03 | 1979-12-11 | Basf Wyandotte Corporation | Amine-coupled polyepichlorohydrin and polyamines derived therefrom |
| US4281199A (en) * | 1978-06-03 | 1981-07-28 | Basf Wyandotte Corporation | Polyalkylene polyamine ether derivatives of polyoxyalkylene compounds |
| CH636898A5 (de) | 1978-10-03 | 1983-06-30 | Sandoz Ag | Waessrige druckfarbenzubereitungen. |
| US4261704A (en) * | 1979-06-22 | 1981-04-14 | Basf Wyandotte Corporation | Polyoxyalkylene polyamine detergent compositions |
| CH667362GA3 (OSRAM) | 1981-03-23 | 1988-10-14 | ||
| JPS6045910U (ja) * | 1983-09-06 | 1985-04-01 | 昭和電線電纜株式会社 | トルクボルト・ナット |
| US5089619A (en) * | 1984-08-30 | 1992-02-18 | Petrolite Corporation | Methods for treating hydrocarbon recovery operations and industrial waters |
| DE3783772T2 (de) * | 1987-06-22 | 1993-05-13 | Nippon Catalytic Chem Ind | Verfahren zur herstellung kationischer wasserloeschlicher harze sowie mittel zur behandlung von wasser. |
| US5364462A (en) * | 1991-08-14 | 1994-11-15 | Graphic Utilities, Incorporated | Waterfast inks |
| US5247087A (en) * | 1992-05-13 | 1993-09-21 | Baker Hughes Incorporated | Epoxy modified water clarifiers |
| 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 |
| DE19621697A1 (de) * | 1996-05-30 | 1997-12-04 | Wolff Walsrode Ag | Verfahren zur Herstellung von Retentions- und Entwässerungsmittel auf Basis von Polyaminoethern |
| GB9813246D0 (en) * | 1998-06-22 | 1998-08-19 | Clariant Int Ltd | Improvements in or relating to organic compounds |
| GB9923921D0 (en) * | 1999-10-08 | 1999-12-08 | Unilever Plc | Fabric care composition |
| CA2351253A1 (en) * | 2000-11-10 | 2002-05-10 | Groupe Lysac Inc./Lysac Group Inc. | Crosslinked polysaccharide, obtained by crosslinking with substituted polyethylene glycol, as superabsorbent |
| JP2006518776A (ja) * | 2003-01-17 | 2006-08-17 | クラリアント インターナショナル リミティド | ポリマーエーテルアミン、それらの製造及び使用 |
| EP1702099A2 (en) * | 2003-12-29 | 2006-09-20 | Clariant International Ltd. | Use of polymeric etheramines for improving the chlorine fastness of textiles |
| CN109503389B (zh) * | 2019-01-14 | 2021-08-31 | 南京师范大学 | 采用单侧线减压精馏与柱层析提取200号聚醚胺中伯胺的方法 |
| CN114717020B (zh) * | 2021-12-28 | 2023-09-26 | 中海油惠州石化有限公司 | 油浆脱固剂及其制备方法和应用以及催化裂化油浆脱固的方法 |
-
1970
- 1970-06-05 CH CH845670A patent/CH541595A/de not_active IP Right Cessation
-
1971
- 1971-05-28 US US00148148A patent/US3753931A/en not_active Expired - Lifetime
- 1971-06-01 GB GB1848071*[A patent/GB1341058A/en not_active Expired
- 1971-06-01 DE DE2127082A patent/DE2127082C3/de not_active Expired
- 1971-06-03 ES ES391897A patent/ES391897A1/es not_active Expired
- 1971-06-03 NL NL717107619A patent/NL146184B/xx unknown
- 1971-06-03 SU SU1666628A patent/SU460632A3/ru active
- 1971-06-04 SE SE7107257A patent/SE376622B/xx unknown
- 1971-06-04 IT IT68891/71A patent/IT943404B/it active
- 1971-06-04 ZA ZA713624A patent/ZA713624B/xx unknown
- 1971-06-04 DD DD155576A patent/DD97892A5/xx unknown
- 1971-06-04 JP JP46039215A patent/JPS5229359B1/ja active Pending
- 1971-06-04 CA CA114798A patent/CA922045A/en not_active Expired
- 1971-06-04 SE SE7402298A patent/SE390647B/xx unknown
- 1971-06-07 BE BE768202A patent/BE768202A/xx unknown
- 1971-06-07 FR FR7120492A patent/FR2094084B1/fr not_active Expired
-
1976
- 1976-12-23 HK HK807/76*UA patent/HK80776A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DD97892A5 (OSRAM) | 1973-05-20 |
| HK80776A (en) | 1976-12-31 |
| JPS5229359B1 (OSRAM) | 1977-08-01 |
| SE376622B (OSRAM) | 1975-06-02 |
| NL146184B (nl) | 1975-06-16 |
| GB1341058A (en) | 1973-12-19 |
| FR2094084A1 (OSRAM) | 1972-02-04 |
| FR2094084B1 (OSRAM) | 1974-08-19 |
| CA922045A (en) | 1973-02-27 |
| DE2127082B2 (de) | 1974-01-24 |
| ES391897A1 (es) | 1974-06-01 |
| NL7107619A (OSRAM) | 1971-12-07 |
| IT943404B (it) | 1973-04-02 |
| SE390647B (sv) | 1977-01-03 |
| DE2127082A1 (de) | 1971-12-09 |
| DE2127082C3 (de) | 1974-08-22 |
| CH541595A (de) | 1973-09-15 |
| ZA713624B (en) | 1973-01-31 |
| BE768202A (fr) | 1971-11-03 |
| US3753931A (en) | 1973-08-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU460632A3 (ru) | Способ получени водорастворимых азотсодержащих полимеров | |
| US3591529A (en) | Phophorus-containing polyamines | |
| US3125552A (en) | Epoxidized poly amides | |
| US3239491A (en) | Resin for wet strength paper | |
| US3784649A (en) | High molecular weight ionene polymeric compositions | |
| JPH01229027A (ja) | 窒素含有水溶性化合物 | |
| ZA200401323B (en) | Optical brighteners, their composition, their production and their use. | |
| CN1926093B (zh) | 合成的多季铵盐 | |
| JPS6244080B2 (OSRAM) | ||
| US4250112A (en) | Polyalkylenepolyamines containing quaternary dialkylammonium groups | |
| US2849411A (en) | Stabilization of basic condensation products of epichlorohydrin | |
| US3715335A (en) | Linear polyester backbone quaternary ammonium polyelectrolytes | |
| US4045377A (en) | Cationic polymer prepared from dicyandiamide, a polyamide, a dialkylamine, and an epoxide | |
| JPH11504966A (ja) | 架橋カチオン性ポリマーの製造方法 | |
| JP5083998B2 (ja) | 汚泥脱水剤及び汚泥脱水方法 | |
| JP2009293049A (ja) | ポリカチオン性ポリ四級生成物、またはそれを含む水性組成物 | |
| US3575797A (en) | Method of recovering fibers and fillers from waste water of paper machines wherein use is made of an ether reaction product comprising a polyamine and a derivative of a polyol having at least two chloroformic acid ester groups | |
| US4184019A (en) | Oxidatively stable ion exchange resin condensation product of an epichlorohydrin and a polyamine | |
| US4283546A (en) | 1,2,4-Triglycidyl triazolidines-3,5-diones and a process for the preparation thereof | |
| US3732173A (en) | Manufacture of water-soluble cationic non-thermosetting methylamine-epichlorohydrin polymer at constant temperature | |
| US6906133B2 (en) | Polyalkyldiallylamine-epihalohydrin resins as wet strength additives for papermaking and process for making the same | |
| US3313742A (en) | High molecular weight alpha, beta-chlorohydrin ether condensation products and theirpreparation | |
| JP2002519442A5 (OSRAM) | ||
| US3275588A (en) | Ethylenimine-polyalkylenepolyamine-polyepihalohydrin terpolymer flocculants | |
| JPH0216304B2 (OSRAM) |