RU2422933C2 - Магнитореологическая композиция - Google Patents

Магнитореологическая композиция Download PDF

Info

Publication number: RU2422933C2
Authority: RU; Russia
Prior art keywords: ethyl; methyl; methylimidazolium; butyl; magnetorheological
Prior art date: 2006-09-22

Application number

RU2009114863/07A

Other languages

English (en)

Russian (ru)

Other versions

RU2009114863A (ru

Inventor

Кристоффер КИБУРГ (DE)

Кристоффер КИБУРГ

Юрген ПФИСТЕР (DE)

Юрген ПФИСТЕР

Клаус ГАБРИЕЛЬ (DE)

Клаус ГАБРИЕЛЬ

Гюнтер ОТТЕР (DE)

Гюнтер ОТТЕР

Мартин ЛАУН (DE)

Мартин ЛАУН

Рене ЛОХТМАН (DE)

Рене Лохтман

Original Assignee

Басф Се

Priority date (The priority date 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 date listed.)

2006-09-22

Filing date

2007-09-18

Publication date

2011-06-27

2007-09-18 Application filed by Басф Се filed Critical Басф Се

2010-10-27 Publication of RU2009114863A publication Critical patent/RU2009114863A/ru

2011-06-27 Application granted granted Critical

2011-06-27 Publication of RU2422933C2 publication Critical patent/RU2422933C2/ru

Links

239000000203 mixture Substances 0.000 title claims abstract description 118
239000002245 particle Substances 0.000 claims abstract description 76
239000002608 ionic liquid Substances 0.000 claims abstract description 38
239000000654 additive Substances 0.000 claims abstract description 30
150000001450 anions Chemical class 0.000 claims abstract description 20
239000000126 substance Substances 0.000 claims abstract description 20
150000001768 cations Chemical class 0.000 claims abstract description 19
230000000996 additive effect Effects 0.000 claims abstract description 7
-1 1-butyl-3-methylimidazolium tetrafluoroborate Chemical compound 0.000 claims description 434
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 47
239000007788 liquid Substances 0.000 claims description 30
239000002270 dispersing agent Substances 0.000 claims description 17
239000003795 chemical substances by application Substances 0.000 claims description 13
239000013008 thixotropic agent Substances 0.000 claims description 10
229910052742 iron Inorganic materials 0.000 claims description 9
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 7
VASPYXGQVWPGAB-UHFFFAOYSA-M 1-ethyl-3-methylimidazol-3-ium;thiocyanate Chemical compound [S-]C#N.CCN1C=C[N+](C)=C1 VASPYXGQVWPGAB-UHFFFAOYSA-M 0.000 claims description 5
238000005260 corrosion Methods 0.000 claims description 5
239000004034 viscosity adjusting agent Substances 0.000 claims description 5
BSKSXTBYXTZWFI-UHFFFAOYSA-M 1-butyl-3-methylimidazol-3-ium;acetate Chemical compound CC([O-])=O.CCCC[N+]=1C=CN(C)C=1 BSKSXTBYXTZWFI-UHFFFAOYSA-M 0.000 claims description 4
SIXHYMZEOJSYQH-UHFFFAOYSA-M 1-butyl-3-methylimidazol-3-ium;thiocyanate Chemical compound [S-]C#N.CCCCN1C=C[N+](C)=C1 SIXHYMZEOJSYQH-UHFFFAOYSA-M 0.000 claims description 4
VRFOKYHDLYBVAL-UHFFFAOYSA-M 1-ethyl-3-methylimidazol-3-ium;ethyl sulfate Chemical compound CCOS([O-])(=O)=O.CCN1C=C[N+](C)=C1 VRFOKYHDLYBVAL-UHFFFAOYSA-M 0.000 claims description 4
MKHFCTXNDRMIDR-UHFFFAOYSA-N cyanoiminomethylideneazanide;1-ethyl-3-methylimidazol-3-ium Chemical compound [N-]=C=NC#N.CCN1C=C[N+](C)=C1 MKHFCTXNDRMIDR-UHFFFAOYSA-N 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 4
239000002562 thickening agent Substances 0.000 claims description 4
YWHZQHRLNXKZNA-UHFFFAOYSA-M 1-ethyl-3-methylimidazol-3-ium;2-(2-methoxyethoxy)ethyl sulfate Chemical compound CC[N+]=1C=CN(C)C=1.COCCOCCOS([O-])(=O)=O YWHZQHRLNXKZNA-UHFFFAOYSA-M 0.000 claims description 3
XIYUIMLQTKODPS-UHFFFAOYSA-M 1-ethyl-3-methylimidazol-3-ium;acetate Chemical compound CC([O-])=O.CC[N+]=1C=CN(C)C=1 XIYUIMLQTKODPS-UHFFFAOYSA-M 0.000 claims description 3
ZTLWMUBOQHZKNS-UHFFFAOYSA-M 1-ethyl-3-methylpyridin-1-ium;ethyl sulfate Chemical compound CCOS([O-])(=O)=O.CC[N+]1=CC=CC(C)=C1 ZTLWMUBOQHZKNS-UHFFFAOYSA-M 0.000 claims description 3
239000006096 absorbing agent Substances 0.000 claims description 3
239000003963 antioxidant agent Substances 0.000 claims description 3
229910017052 cobalt Inorganic materials 0.000 claims description 3
239000010941 cobalt Substances 0.000 claims description 3
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 3
230000008878 coupling Effects 0.000 claims description 3
238000010168 coupling process Methods 0.000 claims description 3
238000005859 coupling reaction Methods 0.000 claims description 3
229910052759 nickel Inorganic materials 0.000 claims description 3
LAGQNGWYNLUQRI-UHFFFAOYSA-N trioctylmethylammonium bis(trifluoromethylsulfonyl)imide Chemical compound FC(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F.CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC LAGQNGWYNLUQRI-UHFFFAOYSA-N 0.000 claims description 3
IRSVMGYCAXSOCN-UHFFFAOYSA-N 1-butyl-3-methyl-1,2-dihydroimidazol-1-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.CCCC[NH+]1CN(C)C=C1 IRSVMGYCAXSOCN-UHFFFAOYSA-N 0.000 claims 1
230000001050 lubricating effect Effects 0.000 claims 1
230000000694 effects Effects 0.000 abstract description 2
230000006866 deterioration Effects 0.000 abstract 1
230000005611 electricity Effects 0.000 abstract 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 60
229910052739 hydrogen Inorganic materials 0.000 description 59
239000001257 hydrogen Substances 0.000 description 59
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 42
230000005291 magnetic effect Effects 0.000 description 35
125000000217 alkyl group Chemical group 0.000 description 34
125000004432 carbon atom Chemical group C* 0.000 description 34
125000005842 heteroatom Chemical group 0.000 description 33
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 29
150000002431 hydrogen Chemical class 0.000 description 28
150000002500 ions Chemical class 0.000 description 27
125000003118 aryl group Chemical group 0.000 description 26
125000000524 functional group Chemical group 0.000 description 26
229910052736 halogen Inorganic materials 0.000 description 26
150000002367 halogens Chemical class 0.000 description 25
229910052757 nitrogen Inorganic materials 0.000 description 22
229910052760 oxygen Inorganic materials 0.000 description 19
239000001301 oxygen Substances 0.000 description 19
125000003545 alkoxy group Chemical group 0.000 description 18
125000004104 aryloxy group Chemical group 0.000 description 18
125000004434 sulfur atom Chemical group 0.000 description 17
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 15
229910052799 carbon Inorganic materials 0.000 description 14
125000000623 heterocyclic group Chemical group 0.000 description 14
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 13
239000012530 fluid Substances 0.000 description 12
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 12
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
125000004433 nitrogen atom Chemical group N* 0.000 description 12
150000001875 compounds Chemical class 0.000 description 11
150000004760 silicates Chemical class 0.000 description 11
125000001841 imino group Chemical group [H]N=* 0.000 description 10
229910052751 metal Inorganic materials 0.000 description 10
239000002184 metal Substances 0.000 description 10
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 9
229910004283 SiO 4 Inorganic materials 0.000 description 9
239000000843 powder Substances 0.000 description 9
150000003839 salts Chemical class 0.000 description 9
229920006395 saturated elastomer Polymers 0.000 description 9
ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 8
230000000052 comparative effect Effects 0.000 description 8
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 8
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 8
125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 7
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 7
239000000460 chlorine Substances 0.000 description 7
230000008021 deposition Effects 0.000 description 7
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 7
229920013639 polyalphaolefin Polymers 0.000 description 7
238000000926 separation method Methods 0.000 description 7
239000004094 surface-active agent Substances 0.000 description 7
ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 6
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 6
229910019142 PO4 Inorganic materials 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
229940094522 laponite Drugs 0.000 description 6
XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 6
238000005259 measurement Methods 0.000 description 6
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
235000021317 phosphate Nutrition 0.000 description 6
229920000642 polymer Polymers 0.000 description 6
150000003512 tertiary amines Chemical class 0.000 description 6
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 5
241000871495 Heeria argentea Species 0.000 description 5
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 5
150000001412 amines Chemical class 0.000 description 5
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 5
230000015572 biosynthetic process Effects 0.000 description 5
150000001721 carbon Chemical group 0.000 description 5
150000002148 esters Chemical class 0.000 description 5
238000002474 experimental method Methods 0.000 description 5
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 5
239000003921 oil Substances 0.000 description 5
239000007787 solid Substances 0.000 description 5
238000012360 testing method Methods 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
NJMWOUFKYKNWDW-UHFFFAOYSA-N 1-ethyl-3-methylimidazolium Chemical compound CCN1C=C[N+](C)=C1 NJMWOUFKYKNWDW-UHFFFAOYSA-N 0.000 description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
125000004429 atom Chemical group 0.000 description 4
230000008859 change Effects 0.000 description 4
229910052801 chlorine Inorganic materials 0.000 description 4
OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 4
150000004820 halides Chemical class 0.000 description 4
125000004356 hydroxy functional group Chemical group O* 0.000 description 4
238000000034 method Methods 0.000 description 4
125000004430 oxygen atom Chemical group O* 0.000 description 4
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 4
239000002244 precipitate Substances 0.000 description 4
239000000523 sample Substances 0.000 description 4
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
229910052717 sulfur Inorganic materials 0.000 description 4
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Natural products C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 4
125000003944 tolyl group Chemical group 0.000 description 4
MEMNKNZDROKJHP-UHFFFAOYSA-M 1-butyl-3-methylimidazol-3-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.CCCCN1C=C[N+](C)=C1 MEMNKNZDROKJHP-UHFFFAOYSA-M 0.000 description 3
MCMFEZDRQOJKMN-UHFFFAOYSA-N 1-butylimidazole Chemical compound CCCCN1C=CN=C1 MCMFEZDRQOJKMN-UHFFFAOYSA-N 0.000 description 3
RVEJOWGVUQQIIZ-UHFFFAOYSA-N 1-hexyl-3-methylimidazolium Chemical compound CCCCCCN1C=C[N+](C)=C1 RVEJOWGVUQQIIZ-UHFFFAOYSA-N 0.000 description 3
125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 3
125000004398 2-methyl-2-butyl group Chemical group CC(C)(CC)* 0.000 description 3
125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 3
WXMVWUBWIHZLMQ-UHFFFAOYSA-N 3-methyl-1-octylimidazolium Chemical compound CCCCCCCCN1C=C[N+](C)=C1 WXMVWUBWIHZLMQ-UHFFFAOYSA-N 0.000 description 3
125000004917 3-methyl-2-butyl group Chemical group CC(C(C)*)C 0.000 description 3
125000004919 3-methyl-2-pentyl group Chemical group CC(C(C)*)CC 0.000 description 3
125000004921 3-methyl-3-pentyl group Chemical group CC(CC)(CC)* 0.000 description 3
125000006201 3-phenylpropyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
125000004920 4-methyl-2-pentyl group Chemical group CC(CC(C)*)C 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
229920002396 Polyurea Polymers 0.000 description 3
KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 3
WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
229920004482 WACKER® Polymers 0.000 description 3
125000002015 acyclic group Chemical group 0.000 description 3
230000002776 aggregation Effects 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
150000003973 alkyl amines Chemical class 0.000 description 3
239000000956 alloy Substances 0.000 description 3
125000000129 anionic group Chemical group 0.000 description 3
239000000440 bentonite Substances 0.000 description 3
229910000278 bentonite Inorganic materials 0.000 description 3
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 3
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
125000004122 cyclic group Chemical group 0.000 description 3
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 3
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 3
238000001704 evaporation Methods 0.000 description 3
230000008020 evaporation Effects 0.000 description 3
229910000271 hectorite Inorganic materials 0.000 description 3
KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 description 3
230000002209 hydrophobic effect Effects 0.000 description 3
MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 3
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 3
239000000463 material Substances 0.000 description 3
229910052901 montmorillonite Inorganic materials 0.000 description 3
LEHULSCLOPRJSL-UHFFFAOYSA-N n,n-dibutylpentan-1-amine Chemical compound CCCCCN(CCCC)CCCC LEHULSCLOPRJSL-UHFFFAOYSA-N 0.000 description 3
125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 3
125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 3
XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 3
150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
229920000728 polyester Polymers 0.000 description 3
238000001556 precipitation Methods 0.000 description 3
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238000005956 quaternization reaction Methods 0.000 description 3
229920002545 silicone oil Polymers 0.000 description 3
239000012798 spherical particle Substances 0.000 description 3
150000003871 sulfonates Chemical class 0.000 description 3
239000011593 sulfur Substances 0.000 description 3
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 3
229920002554 vinyl polymer Polymers 0.000 description 3
125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 description 2
NUERQGVFBSQRBK-UHFFFAOYSA-N 1-butyl-3,4,5-trimethyl-2h-imidazole Chemical compound CCCCN1CN(C)C(C)=C1C NUERQGVFBSQRBK-UHFFFAOYSA-N 0.000 description 2
IQQRAVYLUAZUGX-UHFFFAOYSA-N 1-butyl-3-methylimidazolium Chemical compound CCCCN1C=C[N+](C)=C1 IQQRAVYLUAZUGX-UHFFFAOYSA-N 0.000 description 2
YBGBJKWJBJBEBQ-UHFFFAOYSA-M 1-ethyl-3-methylimidazol-3-ium;hexyl sulfate Chemical compound CC[N+]=1C=CN(C)C=1.CCCCCCOS([O-])(=O)=O YBGBJKWJBJBEBQ-UHFFFAOYSA-M 0.000 description 2
BXSDLSWVIAITRQ-UHFFFAOYSA-M 1-ethyl-3-methylimidazol-3-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.CCN1C=C[N+](C)=C1 BXSDLSWVIAITRQ-UHFFFAOYSA-M 0.000 description 2
FROQVHAYMSVXTG-UHFFFAOYSA-N 1-hexyl-2h-pyridine Chemical compound CCCCCCN1CC=CC=C1 FROQVHAYMSVXTG-UHFFFAOYSA-N 0.000 description 2
AMKUSFIBHAUBIJ-UHFFFAOYSA-N 1-hexylpyridin-1-ium Chemical compound CCCCCC[N+]1=CC=CC=C1 AMKUSFIBHAUBIJ-UHFFFAOYSA-N 0.000 description 2
MCTWTZJPVLRJOU-UHFFFAOYSA-O 1-methylimidazole Chemical compound CN1C=C[NH+]=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-O 0.000 description 2
LJOSVSJNDPICFP-UHFFFAOYSA-N 1-octyl-2h-pyridine Chemical compound CCCCCCCCN1CC=CC=C1 LJOSVSJNDPICFP-UHFFFAOYSA-N 0.000 description 2
XDEQOBPALZZTCA-UHFFFAOYSA-N 1-octylpyridin-1-ium Chemical compound CCCCCCCC[N+]1=CC=CC=C1 XDEQOBPALZZTCA-UHFFFAOYSA-N 0.000 description 2
125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 description 2
KEQTWHPMSVAFDA-UHFFFAOYSA-N 2,3-dihydro-1h-pyrazole Chemical compound C1NNC=C1 KEQTWHPMSVAFDA-UHFFFAOYSA-N 0.000 description 2
KLIDCXVFHGNTTM-UHFFFAOYSA-N 2,6-dimethoxyphenol Chemical group COC1=CC=CC(OC)=C1O KLIDCXVFHGNTTM-UHFFFAOYSA-N 0.000 description 2
125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 2
125000003006 2-dimethylaminoethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 2
125000004918 2-methyl-2-pentyl group Chemical group CC(C)(CCC)* 0.000 description 2
125000004922 2-methyl-3-pentyl group Chemical group CC(C)C(CC)* 0.000 description 2
QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 2
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GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 description 1
125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
125000002948 undecyl group Chemical group [H]C([*])([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])[H] 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1

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SE535675C2 (sv) *	2011-03-22	2012-11-06		Högprestandasmörjmedel och tillsatser till smörjmedel för järnhaltiga och icke järnhaltiga material
CN103305324A (zh) *	2013-05-27	2013-09-18	重庆绿色智能技术研究院	离子液体作为磁流变液基液的应用和基于离子液体的磁流变液及其制备方法
CN103265994A (zh) *	2013-05-27	2013-08-28	重庆绿色智能技术研究院	一种基于多功能化离子液体的磁流变液及其制备方法
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CN112159700B (zh) *	2020-09-04	2021-10-12	清华大学	一种磁流变液组合物及其制备方法
CN116410805B (zh) *	2021-12-30	2025-01-21	中国石油天然气股份有限公司	一种润滑油添加剂及润滑油

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ATE544165T1 (de)	2012-02-15
CN101542647A (zh)	2009-09-23
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RU2009114863A (ru)	2010-10-27
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