Functionalization and Polymerization on the CNT Surfaces

被引:4
作者
Albuerne, Julio [2 ]
Zenkel, Christian [1 ,2 ]
Munirasu, Selvaraj [2 ,3 ]
机构
[1] Fraunhofer Inst Silicate Res ISC, Ctr High Temp Mat & Design, D-97082 Wurzburg, Germany
[2] Helmholtz Zentrum Geesthacht, Polymer Res Inst, D-21502 Geesthacht, Germany
[3] King Abdullah Univ Sci & Technol, Water Desalinat & Reuse Ctr, Thuwal, Saudi Arabia
关键词
Carbon nano tubes; Controlled radical polymerizations; Functionalization; Grafting from; Grafting to; Grafting through; Nanocomposite; WALLED-CARBON-NANOTUBES; TRANSFER RADICAL POLYMERIZATION; RING-OPENING POLYMERIZATION; FRAGMENTATION CHAIN-TRANSFER; IN-SITU SYNTHESIS; RAFT POLYMERIZATION; INITIATED POLYMERIZATION; POLYSTYRENE; COMPOSITES; POLYMERS;
D O I
10.2174/13852728113179990088
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In this review we focus on the current status of using carbon nanotube (CNT) as a filler for polymer nanocomposites. Starting with the historical background of CNT, its distinct properties and the surface functionalization of the nanotube, the three different surface polymerization techniques, namely grafting "from", "to" and "through/in between" were discussed. Wider focus has been given on "grafting from" surface initiated polymerizations, including atom transfer radical polymerization (ATRP), reversible addition fragmentation chain-transfer (RAFT) Polymerization, nitroxide mediated polymerization (NMP), ring opening polymerization (ROP) and other miscellaneous polymerization methods. The grafting "to" and "through/in between" also discussed and compared with grafting from polymerization. The merits and shortcomings of all three grafting methods were discussed and the bottleneck issue in grafting from method has been highlighted. Furthermore the current and potential future industrial applications were deliberated. Finally the toxicity issue of CNTs in the final product has been reviewed with the limited available literature knowledge.
引用
收藏
页码:1867 / 1879
页数:13
相关论文
共 112 条
[1]   Enhanced mechanical and photoluminescence effect of poly(l-lactide) reinforced with functionalized multiwalled carbon nanotubes [J].
Amirian, Maryam ;
Chakoli, Ali Nabipour ;
Sui, Jie He ;
Cai, Wei .
POLYMER BULLETIN, 2012, 68 (06) :1747-1763
[2]  
[Anonymous], 2010, PRODUCTION APPL CARB
[3]  
[Anonymous], 2005, FUNCTIONAL MOL NANOS
[4]  
[Anonymous], 2007, CARB NAN TECHN COMM
[5]   Molecular electronics with carbon nanotubes [J].
Avouris, P .
ACCOUNTS OF CHEMICAL RESEARCH, 2002, 35 (12) :1026-1034
[6]   Polymer-grafted multiwalled carbon nanotubes through surface-initiated polymerization [J].
Baskaran, D ;
Mays, JW ;
Bratcher, MS .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (16) :2138-2142
[7]   Polymer adsorption in the grafting reactions of hydroxyl terminal polymers with multi-walled carbon nanotubes [J].
Baskaran, D ;
Mays, JW ;
Bratcher, MS .
POLYMER, 2005, 46 (14) :5050-5057
[8]   A generic organometallic approach toward ultra-strong carbon nanotube polymer composites [J].
Blake, R ;
Gun'ko, YK ;
Coleman, J ;
Cadek, M ;
Fonseca, A ;
Nagy, JB ;
Blau, WJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (33) :10226-10227
[9]   Reinforcement of poly(vinyl chloride) and polystyrene using chlorinated polypropylene grafted carbon nanotubes [J].
Blake, Rowan ;
Coleman, Jonathan N. ;
Byrne, Michele T. ;
McCarthy, Joseph E. ;
Perova, Tatiana S. ;
Blau, Werner J. ;
Fonseca, Antonio ;
Nagy, Janos B. ;
Gun'ko, Yurii K. .
JOURNAL OF MATERIALS CHEMISTRY, 2006, 16 (43) :4206-4213
[10]   Side-wall functionalization of single-walled carbon nanotubes with 4-hydroxymethylaniline followed by polymerization of ε-caprolactone [J].
Buffa, F ;
Hu, H ;
Resasco, DE .
MACROMOLECULES, 2005, 38 (20) :8258-8263