SU591133A3 - Способ получени водных растворов бромистых комплексных соединений с неиногенными поверхностно-активными веществами - Google Patents
Способ получени водных растворов бромистых комплексных соединений с неиногенными поверхностно-активными веществамиInfo
- Publication number
- SU591133A3 SU591133A3 SU741994696A SU1994696A SU591133A3 SU 591133 A3 SU591133 A3 SU 591133A3 SU 741994696 A SU741994696 A SU 741994696A SU 1994696 A SU1994696 A SU 1994696A SU 591133 A3 SU591133 A3 SU 591133A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- water
- temperature
- reaction
- added
- ethylene oxide
- Prior art date
Links
- 239000007864 aqueous solution Substances 0.000 title claims 6
- 239000013543 active substance Substances 0.000 title 1
- 150000001649 bromium compounds Chemical class 0.000 title 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 22
- 238000006243 chemical reaction Methods 0.000 claims 14
- 239000000243 solution Substances 0.000 claims 14
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 12
- 150000001875 compounds Chemical class 0.000 claims 11
- 238000000354 decomposition reaction Methods 0.000 claims 10
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 claims 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 8
- 150000003839 salts Chemical class 0.000 claims 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 6
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 claims 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims 6
- 239000007788 liquid Substances 0.000 claims 6
- -1 hydroxyethyl fatty alcohol Chemical class 0.000 claims 5
- 239000011541 reaction mixture Substances 0.000 claims 5
- 235000011007 phosphoric acid Nutrition 0.000 claims 4
- 239000000126 substance Substances 0.000 claims 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims 3
- 229930195729 fatty acid Natural products 0.000 claims 3
- 239000000194 fatty acid Substances 0.000 claims 3
- 229940102396 methyl bromide Drugs 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 239000002736 nonionic surfactant Substances 0.000 claims 3
- 235000007715 potassium iodide Nutrition 0.000 claims 3
- 229960004839 potassium iodide Drugs 0.000 claims 3
- 238000002360 preparation method Methods 0.000 claims 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 claims 3
- XDRNWSFXWXJHEN-UHFFFAOYSA-L Br[K].Br[K] Chemical compound Br[K].Br[K] XDRNWSFXWXJHEN-UHFFFAOYSA-L 0.000 claims 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 238000007792 addition Methods 0.000 claims 2
- 235000015278 beef Nutrition 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 239000003153 chemical reaction reagent Substances 0.000 claims 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 claims 2
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 claims 2
- 150000002191 fatty alcohols Chemical class 0.000 claims 2
- HSZCZNFXUDYRKD-UHFFFAOYSA-M lithium iodide Chemical compound [Li+].[I-] HSZCZNFXUDYRKD-UHFFFAOYSA-M 0.000 claims 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 claims 2
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 claims 2
- 238000003756 stirring Methods 0.000 claims 2
- SODQFLRLAOALCF-UHFFFAOYSA-N 1lambda3-bromacyclohexa-1,3,5-triene Chemical compound Br1=CC=CC=C1 SODQFLRLAOALCF-UHFFFAOYSA-N 0.000 claims 1
- BLBYVBAMIDURKR-UHFFFAOYSA-N C(CCCCCCCCCCC)OS(=O)(=O)C(C1=CC=CC=C1)=O.[Na] Chemical compound C(CCCCCCCCCCC)OS(=O)(=O)C(C1=CC=CC=C1)=O.[Na] BLBYVBAMIDURKR-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 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 claims 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 1
- 235000021355 Stearic acid Nutrition 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims 1
- KCZAQYXQAGPIPZ-UHFFFAOYSA-M [K+].[Br-].Br.I Chemical compound [K+].[Br-].Br.I KCZAQYXQAGPIPZ-UHFFFAOYSA-M 0.000 claims 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
- 150000001342 alkaline earth metals Chemical class 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 239000012752 auxiliary agent Substances 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 239000006260 foam Substances 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- AMXOYNBUYSYVKV-UHFFFAOYSA-M lithium bromide Chemical compound [Li+].[Br-] AMXOYNBUYSYVKV-UHFFFAOYSA-M 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 229910001511 metal iodide Inorganic materials 0.000 claims 1
- 150000007522 mineralic acids Chemical class 0.000 claims 1
- XONPDZSGENTBNJ-UHFFFAOYSA-N molecular hydrogen;sodium Chemical compound [Na].[H][H] XONPDZSGENTBNJ-UHFFFAOYSA-N 0.000 claims 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 claims 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims 1
- 150000007524 organic acids Chemical class 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 229920000151 polyglycol Polymers 0.000 claims 1
- 239000010695 polyglycol Substances 0.000 claims 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 235000009518 sodium iodide Nutrition 0.000 claims 1
- 238000001228 spectrum Methods 0.000 claims 1
- 239000007858 starting material Substances 0.000 claims 1
- 239000008117 stearic acid Substances 0.000 claims 1
- 229910021653 sulphate ion Inorganic materials 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 239000003760 tallow Substances 0.000 claims 1
- 239000011975 tartaric acid Substances 0.000 claims 1
- 235000002906 tartaric acid Nutrition 0.000 claims 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL16063173A PL86611B1 (enrdf_load_html_response) | 1973-02-07 | 1973-02-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
SU591133A3 true SU591133A3 (ru) | 1978-01-30 |
Family
ID=19961594
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU741994696A SU591133A3 (ru) | 1973-02-07 | 1974-02-06 | Способ получени водных растворов бромистых комплексных соединений с неиногенными поверхностно-активными веществами |
Country Status (2)
Country | Link |
---|---|
PL (1) | PL86611B1 (enrdf_load_html_response) |
SU (1) | SU591133A3 (enrdf_load_html_response) |
-
1973
- 1973-02-07 PL PL16063173A patent/PL86611B1/pl unknown
-
1974
- 1974-02-06 SU SU741994696A patent/SU591133A3/ru active
Also Published As
Publication number | Publication date |
---|---|
PL86611B1 (enrdf_load_html_response) | 1976-06-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4865774A (en) | Surface-active hydroxysulfonates | |
US4650865A (en) | Process for preparing tertiary ether amines | |
KR101441722B1 (ko) | 계면 활성제 조성물 | |
JPH0248563A (ja) | 4―アルコキシ―2―ヒドロキシベンゾフエノン―5―スルホン酸の製法 | |
JPH0430943B2 (enrdf_load_html_response) | ||
EP0510565B1 (en) | Surface-active agents derived from sulfosuccinic esters | |
US4792419A (en) | Ether sulfonates | |
US5739365A (en) | Method for preparing ammonium hydroxyalkyl sulfonates and ammonium alkanoyl alkyl sulfonates produced therefrom | |
US7241875B2 (en) | Method for the production of surface active agent mixtures | |
EP0295578B1 (de) | Verwendung von Erdalkalisalzen von Ethercarbonsäuren als Katalysatoren für die Alkoxylierung | |
US5480979A (en) | Process for the production of alkyl and/or alkenyl oligoglycosides | |
SU591133A3 (ru) | Способ получени водных растворов бромистых комплексных соединений с неиногенными поверхностно-активными веществами | |
US4226807A (en) | Process for making ether sulfonates | |
JPS60105689A (ja) | 新規ホスホベタイン化合物 | |
NZ231926A (en) | Styrene oxide-alcohol adducts, compositions and use thereof in textile finishing | |
EP0406168B1 (de) | Phenylalkylglycidether-Anlagerungsprodukte | |
WO2002038269A1 (en) | An alkoxylenation catalyst and a method to manufacture the alkoxylenation catalyst | |
JPS54141708A (en) | Preparation of glycidyl ether | |
EP0421326B1 (en) | Transparent toilet soap | |
SU640638A3 (ru) | Способ получени бром-иодистых комплексных соединений с наионогенными поверхностно-активными веществами | |
EP0337239A2 (de) | Verwendung von Erdalkalisalzen von Polycarbonsäuremonoestern als Katalysatoren für die Alkoxylierung | |
US2693482A (en) | Preparation of alkene phosphonous acids | |
JPS559025A (en) | Preparation of polyfluoroalcohol | |
JPH04313337A (ja) | 界面活性剤の安定かつ均一な水性配合物 | |
EP0210642A2 (en) | Surfactants derived from succinic acid |