Recent advance in research on halloysite nanotubes-polymer nanocomposite

被引:758
作者
Liu, Mingxian [1 ]
Jia, Zhixin [2 ]
Jia, Demin [2 ]
Zhou, Changren [1 ]
机构
[1] Jinan Univ, Dept Mat Sci & Engn, Guangzhou 510632, Guangdong, Peoples R China
[2] S China Univ Technol, Coll Mat Sci & Engn, Guangzhou 510640, Guangdong, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
Interfacial interaction; Dispersion; Reinforcing; Flame retardance; Crystallization; Biocompatibility; MECHANICAL-PROPERTIES; SUSTAINED-RELEASE; CLAY NANOTUBES; CRYSTALLIZATION BEHAVIOR; INTERFACIAL INTERACTION; THERMAL-PROPERTIES; COMPOSITES; ACID; MINERALS; COATINGS;
D O I
10.1016/j.progpolymsci.2014.04.004
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Halloysite nanotubes (HNTs) are novel 1D natural nanomaterials with predominantly hollow tubular nanostructures and high aspect ratios. Due to their high mechanical strength, thermal stability, biocompatibility, and abundance, HNTs have a number of exciting potential applications in polymer nanocomposites. In this article, we review the recent progress toward the development of HNTs-polymer nanocomposites, while paying particular attention to interfacial interactions of the nanocomposites. The characteristics of the HNTs relative to the formation of the polymer nanocomposites are summarized first. The covalent or non-covalent functionalization methods for HNTs and various fabrication approaches for HNTs-polymer nanocomposites are introduced afterward. Polymer nanocomposites reinforced with HNTs possess highly increased tensile and flexural strength, elastic moduli, and improved toughness. HNTs-polymer nanocomposites also exhibit elevated thermal resistance, flame retardance and unique crystallization behavior. Due to the tubular microstructure and the biocompatibility of HNTs, HNTs-polymer nanocomposites have demonstrated good drug encapsulation and sustained release abilities, gaining them extensive use as tissue engineering scaffolds and drug carriers. Finally, we summarize the characteristics of HNTs-polymer nanocomposites and predict for the development of the potential applications in high-performance composites for aircraft/automobile industries, environmental protection, and biomaterials. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1498 / 1525
页数:28
相关论文
共 151 条
[1]   Halloysite clay nanotubes as a ceramic "skeleton" for functional biopolymer composites with sustained drug release [J].
Abdullayev, Elshad ;
Lvov, Yuri .
JOURNAL OF MATERIALS CHEMISTRY B, 2013, 1 (23) :2894-2903
[2]   Self-Healing Coatings Based on Halloysite Clay Polymer Composites for Protection of Copper Alloys [J].
Abdullayev, Elshad ;
Abbasov, Vagif ;
Tursunbayeva, Asel ;
Portnov, Vasiliy ;
Ibrahimov, Hikmat ;
Mukhtarova, Gulbaniz ;
Lvov, Yuri .
ACS APPLIED MATERIALS & INTERFACES, 2013, 5 (10) :4464-4471
[3]   Enlargement of Halloysite Clay Nanotube Lumen by Selective Etching of Aluminum Oxide [J].
Abdullayev, Elshad ;
Joshi, Anupam ;
Wei, Wenbo ;
Zhao, Yafei ;
Lvov, Yuri .
ACS NANO, 2012, 6 (08) :7216-7226
[4]   Halloysite Tubes as Nanocontainers for Anticorrosion Coating with Benzotriazole [J].
Abdullayev, Elshad ;
Price, Ronald ;
Shchukin, Dmitry ;
Lvov, Yuri .
ACS APPLIED MATERIALS & INTERFACES, 2009, 1 (07) :1437-1443
[5]   Release kinetics of 5-aminosalicylic acid from halloysite [J].
Aguzzi, C. ;
Viseras, C. ;
Cerezo, P. ;
Salcedo, I. ;
Sanchez-Espejo, R. ;
Valenzuela, C. .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2013, 105 :75-80
[6]   Morphological structures and tribological performance of unsaturated polyester based untreated/silane-treated halloysite nanotubes [J].
Albdiry, M. T. ;
Yousif, B. F. .
MATERIALS & DESIGN, 2013, 48 :68-76
[7]   Water absorption, mechanical, and thermal properties of halloysite nanotube reinforced vinyl-ester nanocomposites [J].
Alhuthali, A. ;
Low, I. M. .
JOURNAL OF MATERIALS SCIENCE, 2013, 48 (12) :4260-4273
[8]  
Ames L. L., 1957, CLAYS CLAY MINER, V6, P378
[9]  
[Anonymous], 2014, HALLOYSITE MINERAL D
[10]  
[Anonymous], 1948, MINERAL MAG J M SOC, DOI DOI 10.1180/MINMAG.1948.028.203.02