Basic amid acid-assisted synthesis of resorcinol-formaldehyde polymer and carbon nanospheres

被引:45
作者
Dong, Yong-Rong [1 ]
Nishiyama, Norikazu [1 ]
Egashira, Yasuyuki [1 ]
Ueyama, Korekazu [1 ]
机构
[1] Osaka Univ, Grad Sch Engn Sci, Div Chem Engn, Osaka 5608531, Japan
关键词
D O I
10.1021/ie7017417
中图分类号
TQ [化学工业];
学科分类号
0817 [化学工程与技术];
摘要
Polymer nanospheres were synthesized through polymerization of resorcinol/formaldehyde (RF) in the presence of a basic amino acid, L-lysine, as a catalyst. The diameters of the RF polymer nanospheres can be tuned in the range of 30-650 nm by adjusting the molar ratios of L-lysine/H2O and resorcinol/H2O in the precursor solutions. The pH of L-lysine solution was reduced from 9.3 to 7.0 just after it was mixed with the RF solution, indicating that L-lysine molecules in the solution were consumed by interacting with resorcinol. As a result, particle growth rate extremely reduces. Thus, the particle size of the RF polymer was not much dependent with synthesis time. Thus, the use of L-lysine facilitates precise control of the size of the RF polymer nanospheres compared to the synthesis using an ammonia solution as a catalyst. Carbonized particles showed the same size as the RF polymer nanospheres. The resulting carbon nanospheres had mesopores and macropores with a surface area of 330-400 m(2)/g.
引用
收藏
页码:4712 / 4716
页数:5
相关论文
共 27 条
[1]
Carbon microspheres obtained from resorcinol-formaldehyde as high-capacity electrodes for sodium-ion batteries [J].
Alcántara, R ;
Lavela, P ;
Ortiz, GF ;
Tirado, JL .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2005, 8 (04) :A222-A225
[2]
Characterisation of mesocarbon microbeads (MCMB) as active electrode material in lithium and sodium cells [J].
Alcántara, R ;
Madrigal, FJF ;
Lavela, P ;
Tirado, JL ;
Mateos, JMJ ;
de Salazar, CG ;
Stoyanova, R ;
Zhecheva, E .
CARBON, 2000, 38 (07) :1031-1041
[3]
Carbons as supports for industrial precious metal catalysts [J].
Auer, E ;
Freund, A ;
Pietsch, J ;
Tacke, T .
APPLIED CATALYSIS A-GENERAL, 1998, 173 (02) :259-271
[4]
Redox-active silica nanoparticles.: Part 1.: Electrochemistry and catalytic activity of spherical, nonporous silica particles with nanometric diameters and covalently bound redox-active modifications [J].
Budny, Anna ;
Novak, Filip ;
Plumere, Nicolas ;
Schetter, Bernd ;
Speiser, Bernd ;
Straub, Diana ;
Mayer, Hermann A. ;
Reginek, Michaela .
LANGMUIR, 2006, 22 (25) :10605-10611
[5]
Mechanistic principles of nanoparticle evolution to zeolite crystals [J].
Davis, TM ;
Drews, TO ;
Ramanan, H ;
He, C ;
Dong, JS ;
Schnablegger, H ;
Katsoulakis, MA ;
Kokkoli, E ;
McCormick, AV ;
Penn, RL ;
Tsapatsis, M .
NATURE MATERIALS, 2006, 5 (05) :400-408
[6]
CARBON ONIONS PRODUCED BY HEAT-TREATMENT OF CARBON SOOT AND THEIR RELATION TO THE 217.5 NM INTERSTELLAR ABSORPTION FEATURE [J].
DEHEER, WA ;
UGARTE, D .
CHEMICAL PHYSICS LETTERS, 1993, 207 (4-6) :480-486
[7]
Spontaneous formation of silica nanoparticles in basic solutions of small tetraalkylammonium cations [J].
Fedeyko, JM ;
Rimer, JD ;
Lobo, RF ;
Vlachos, DG .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (33) :12271-12275
[8]
Carbon materials for lithium-ion rechargeable batteries [J].
Flandrois, S ;
Simon, B .
CARBON, 1999, 37 (02) :165-180
[9]
Influence of surface-active agents on pore characteristics of the generated spherical resorcinol-formaldehyde based carbon aerogels [J].
Horikawa, T ;
Ono, Y ;
Hayashi, J ;
Muroyama, K .
CARBON, 2004, 42 (12-13) :2683-2689
[10]
Horikawa T, 2004, CARBON, V42, P169, DOI [10.1016/j.carbon.2003.10.007, 10.1016/j.carbon.2003.09.007]