Preparation of Poly(1-vinylimidazole)-Grafted Magnetic Nanoparticles and Their Application for Removal of Metal Ions
Source abstract
Abstract
Poly(1-vinylimidazole) with a trimethoxysilyl terminal group (Im n ) was synthesized by telomerization of 1-vinylimidazole. The degree of polymerization ( n ) was determined by 1 H NMR to be 18. The Im 18 with reactive silane terminal group was grafted directly onto nanosize magnetic particles (maghemite, γ-Fe 2 O 3 ) through siloxane bonds to produce polymer-grafted magnetic nanocomposite particles (Mag-Im 18 ). The amount of polymer anchored on the particle was estimated by elemental analysis to be 5 wt %. The surface coverage of imidazolyl groups was estimated to be 0.44 mmol g - 1 . A stable Mag-Im 18 suspension was prepared, and the polymer coatings were chemically stable over a pH range of 3.5−10.0. The Mag-Im 18 showed a selective binding of divalent metal ions with a binding strength in the order of Cu 2+ ≫ Ni 2+ > Co 2+ . At pH 5.3, the limiting adsorption capacity for Cu 2+ ion was 0.11 mmol g - 1 . Selective separation/recovery of Cu 2+ ions from a Cu 2+ /Co 2+ aqueous solution was demonstrated over a pH range of 3−7.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanomaterials for catalytic reactions · Electromagnetic wave absorption materials · Graphene research and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Applied Chemistry & Biochemistry, Faculty of Engineering, Kumamoto University, Kumamoto 860-8555, Japan, and Department of Chemical and Materials Engineering, Faculty of Engineering, University of Alberta, Edmonton, T6G 2G6 Canada
References (53)
Show source-provided references
1. Rosensweig, R.Ferrohydrodynamics; Cambridge University Press: Cambridge, 1985.
2. Sun S. · Science · 2000 · 287 · 198910.1126/science.287.5460.1989 ↗
3. Leslie-Pelecky D. L. · Chem. Mater. · 1996 · 8 · 177010.1021/cm960077f ↗
4. Raj K. · J. Magn. Magn. Mater. · 1990 · 85 · 23310.1016/0304-8853(90)90058-X ↗
5. Speliotis D. E. · J. Magn. Magn. Mater. · 1999 · 193 · 2910.1016/S0304-8853(98)00399-0 ↗
6. Ozaki, M.MRS Bull.1989,December, 35.10.1557/S0883769400060942 ↗
7. Babes L. · J. Colloid Interface Sci. · 1999 · 212 · 47410.1006/jcis.1998.6053 ↗
8. Chemla Y. R. · Natl. Acad. Sci. U.S.A. · 2000 · 97 · 1426810.1073/pnas.97.26.14268 ↗
9. Whitesides G. M. · TIBTEH · 1983 · 114
10. Ugelstad J. · Prog. Polym. Sci. · 1992 · 17 · 8710.1016/0079-6700(92)90017-S ↗
11. Liu Q. · Chem. Mater. · 1998 · 10 · 393610.1021/cm980370a ↗
12. Butterworth M. D. · Colloids Surf. A · 2001 · 179 · 9310.1016/S0927-7757(00)00633-6 ↗
13. Szabo D. V. · Adv. Mater. · 1999 · 11 · 131310.1002/(SICI)1521-4095(199910)11:15<1313::AID-ADMA1313>3.0.CO;2-2 ↗
14. Correa-Duate M. A. · Langmuir · 1998 · 14 · 643010.1021/la9805342 ↗
15. Donselaar L. N. · Langmuir · 1997 · 13 · 601810.1021/la970359+ ↗
16. Suzuki M. · Biotech. Appl. Biochem. · 1995 · 21 · 33510.1111/j.1470-8744.1995.tb00339.x ↗
17. Mihama T. · J. Biotechnol. · 1988 · 7 · 14110.1016/0168-1656(88)90060-0 ↗
18. Yoshimoto T. · Biochem. Biophys. Res. Commun. · 1987 · 145 · 90810.1016/0006-291X(87)91051-5 ↗
19. Butterworth M. D. · Colloids Surf. A · 2001 · 179 · 9310.1016/S0927-7757(00)00633-6 ↗
20. Cocker T. M. · Biotechnol. Bioeng. · 1997 · 53 · 7910.1002/(SICI)1097-0290(19970105)53:1<79::AID-BIT11>3.0.CO;2-4 ↗
21. Manju G. N. · J. Hazardous Mater. · 2002 · 91 · 22110.1016/S0304-3894(01)00392-2 ↗
22. Ding X. B. · React. Funct. Polym. · 1998 · 38 · 1110.1016/S1381-5148(97)00154-5 ↗
23. Hasegawa M. · 1978
24. Molday R. S. · J. Immunol. Methods · 1982 · 52 · 35310.1016/0022-1759(82)90007-2 ↗
25. An X. · J. Appl. Polym. Sci. · 2001 · 81 · 117510.1002/app.1539 ↗
26. Xu Z. · Appl. Surf. Sci. · 1997 · 120 · 26910.1016/S0169-4332(97)00234-1 ↗
27. Browne T. E. · Ind. Eng. Chem. Res. · 1993 · 32 · 71610.1021/ie00016a019 ↗
28. Kanazawa H. · Anal. Chem. · 1997 · 69 · 82310.1021/ac961024k ↗
29. Hirayama C. · Macromol. · 1992 · 25 · 637510.1021/ma00049a041 ↗
30. Ihara H. · Anal. Sci. · 1993 · 9 · 71110.2116/analsci.9.711 ↗
31. Ihara H. · Chem. Lett. · 2001 · 125210.1246/cl.2001.1252 ↗
32. Ihara H. · Anal. Sci. · 1995 · 11 · 73910.2116/analsci.11.739 ↗
33. Ihara H. · Anal. Sci. · 1998 · 14 · 34910.2116/analsci.14.349 ↗
34. Ihara H. · Chem. Lett. · 1997 · 11310.1246/cl.1997.113 ↗
35. Fukumoto T. · J. Chromatogr. · 1994 · 672 · 23710.1016/0021-9673(94)80612-8 ↗
36. Ihara H. · J. Liq. Chromatogr. · 1996 · 19 · 296710.1080/10826079608015120 ↗
37. Takafuji M. · Polym. J. · 2002 · 34 · 43710.1295/polymj.34.437 ↗
38. Gold D. H. · J. Phys. Chem. · 1960 · 64 · 146410.1021/j100839a027 ↗
39. Liu K. J. · J. Phys. Chem. · 1965 · 69 · 125210.1021/j100888a027 ↗
40. Tanford C. · J. Am. Chem. Soc. · 1953 · 75 · 43410.1021/ja01098a052 ↗
41. Gold D. H. · J. Phys. Chem. · 1960 · 64 · 146110.1021/j100839a026 ↗
42. Molina M. J. · J. Appl. Polym. Sci. · 2001 · 79 · 146710.1002/1097-4628(20010222)79:8<1467::AID-APP140>3.0.CO;2-9 ↗
43. Guler H. · J. Appl. Polym. Sci. · 1997 · 66 · 247510.1002/(SICI)1097-4628(19971226)66:13<2475::AID-APP10>3.0.CO;2-X ↗
44. Travers C. · 1974
45. Tsuchida E. · 1974
46. Geckeler K. · Pure Appl. Chem. · 1980 · 52 · 188310.1351/pac198052071883 ↗
47. Kirimura Y. · J. Chem. Soc., Faraday Trans. · 1990 · 86 · 3357
48. Rivas B. L. · Angew. Makromol. Chem. · 1994 · 220 · 6110.1002/apmc.1994.052200106 ↗
49. Zamora M. · Eur. Polym. J. · 1996 · 32 · 12510.1016/0014-3057(95)00111-5 ↗
50. Marthur A. M. · J. Macromol. Sci., Rev. Macromol. Phys. · 1996 · 36 · 40510.1080/15321799608015226 ↗
51. Rivas B. L. · J. Appl. Polym. Sci. · 1998 · 67 · 110910.1002/(SICI)1097-4628(19980207)67:6<1109::AID-APP19>3.0.CO;2-V ↗
52. Pekel N. · Colloid Polym. Sci. · 1999 · 277 · 57010.1007/s003960050426 ↗
53. Edsall J. T. · J. Am. Chem. Soc. · 1954 · 76 · 305410.1021/ja01640a068 ↗