Functionalized Fe3O4 nanoparticles: influence of ligand addition sequence and pH during their continuous hydrothermal synthesis

被引:5
作者
Thomas, G. [1 ]
Demoisson, F. [1 ]
Heintz, O. [1 ]
Geoffroy, N. [1 ]
Saviot, L. [1 ]
Millot, N. [1 ]
机构
[1] Univ Bourgogne Franche Comte, CNRS, Lab Interdisciplinaire Carnot Bourgogne, UMR 6303, F-21078 Dijon, France
来源
RSC ADVANCES | 2015年 / 5卷 / 96期
关键词
IRON-OXIDE NANOPARTICLES; SUPERCRITICAL WATER; L-DOPA; SURFACE FUNCTIONALIZATION; MAGNETITE NANOPARTICLES; OXYGEN STOICHIOMETRY; IN-SITU; OXIDATION; PARTICLES; CHEMISTRY;
D O I
10.1039/c5ra17452j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study we report various new efficient ways to synthesize and modify in situ magnetite (Fe3O4) iron oxide nanoparticles (NPs). Thanks to an apparatus especiay developed for this new method of grafting, the NPs have been synthesized and functionalized by 3,4-dihydroxyhydrocinnamic acid (DHCA) or 3,4-dihydroxy-L-phenyEalanine (LDOPA) in one step and under hydrothermaL conditions using varying concentration ratios ([organic moLecuLes]/[ferrous and ferric ions]). The organic moLecuLes were added before or after the NP synthesis. The addition of these organic moLecuLes modifies the structure, the morphoLogy, the oxidation degree and the growth of the crystahites. Adding the organic moLecuLes before the synthesis step and under acidic conditions increases the average crystaite size and prevents further oxidation whereas under basic conditions the growth is stopped but a partiaL oxidation of magnetite to maghemite NPs is observed. Adding DHCA or LDOPA after the synthesis step results in a modification of the Lattice structure and oxidation degree of the NPs but does not change the average size. This study underlines the importance of the sequence of the addition of organic moLecuLes on the synthesis of NPs.
引用
收藏
页码:78614 / 78624
页数:11
相关论文
共 56 条
  • [1] RAPID AND CONTINUOUS HYDROTHERMAL CRYSTALLIZATION OF METAL-OXIDE PARTICLES IN SUPERCRITICAL WATER
    ADSCHIRI, T
    KANAZAWA, K
    ARAI, K
    [J]. JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1992, 75 (04) : 1019 - 1022
  • [2] Continuous hydrothermal synthesis of nanometric BaZrO3 in supercritical water
    Aimable, A.
    Xin, B.
    Millot, N.
    Aymes, D.
    [J]. JOURNAL OF SOLID STATE CHEMISTRY, 2008, 181 (01) : 183 - 189
  • [3] Influence of Electronegative Substituents on the Binding Affinity of Catechol-Derived Anchors to Fe3O4 Nanoparticles
    Amstad, Esther
    Gehring, Andreas U.
    Fischer, Hakon
    Nagaiyanallur, Venkatamaran V.
    Haehner, Georg
    Textor, Marcus
    Reimhult, Erik
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2011, 115 (03) : 683 - 691
  • [4] Aymes D., 2011, Patent No. [WO 2011010056 A1, 2011010056]
  • [5] Barreto WJ, 1999, SPECTROCHIM ACTA A, V55, P65
  • [6] In situ and time resolved study of the γ/α-Fe2O3 transition in nanometric particles
    Belin, T.
    Millot, N.
    Bovet, N.
    Gailhanou, M.
    [J]. JOURNAL OF SOLID STATE CHEMISTRY, 2007, 180 (08) : 2377 - 2385
  • [7] Structural variations as a function of surface adsorption in nanostructured particles
    Belin, T
    Millot, N
    Villiéras, F
    Bertrand, O
    Bellat, JP
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (17) : 5333 - 5340
  • [8] Influence of grain size, oxygen stoichiometry, and synthesis conditions on the γ-Fe2O3 vacancies ordering and lattice parameters
    Belin, T
    Guigue-Millot, N
    Caillot, T
    Aymes, D
    Niepce, JC
    [J]. JOURNAL OF SOLID STATE CHEMISTRY, 2002, 163 (02) : 459 - 465
  • [9] Studies on enzymatic oxidation of 3′,4′-dihydroxy-L-phenylalanine to dopachrome using kinetic isotope effect methods
    Byszewska, Wioleta
    Kanska, Marianna
    [J]. JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY, 2014, 299 (03) : 1373 - 1378
  • [10] Synthesis of FePt nanocubes and their oriented self-assembly
    Chen, Min
    Kim, Jaemin
    Liu, J. P.
    Fan, Hongyou
    Sun, Shouheng
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (22) : 7132 - 7133