Effects of modified LDPE on physico-mechanical properties of HDPE/CaCO3 composites

被引:10
作者
Ahn, Youngjun [1 ]
Jeon, Jong Hyuk [1 ]
Park, Ju-Hyoung [2 ]
Thenepalli, Thriveni [3 ]
Ahn, Ji Whan [3 ]
Han, Choon [1 ]
机构
[1] Kwangwoon Univ, Dept Chem Engn, 20 Gwangun Ro, Seoul 01897, South Korea
[2] Korea Inst Energy Res, Clean Fuel Lab, 71-2 Jang Dong, Daejeon 34129, South Korea
[3] Korea Inst Geosci & Mineral Resources, Mineral Resources Res Div, 124 Gwahak Ro, Daejeon 34132, South Korea
关键词
Low Density Polyethylene; Maleic Anhydride; High Density Polyethylene; Calcium Carbonate; Polymer Composite; HIGH-DENSITY POLYETHYLENE; CALCIUM-CARBONATE COMPOSITES; MALEIC-ANHYDRIDE; POLYPROPYLENE COMPOSITES; MECHANICAL-PROPERTIES; CACO3; NANOPARTICLES; REACTIVE EXTRUSION; TENSILE PROPERTIES; NANOCOMPOSITES; BEHAVIOR;
D O I
10.1007/s11814-016-0159-6
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
HDPE/CaCO3/LDPE-g-MA composites of high density polyethylene (HDPE) and calcium carbonate (CaCO3) with maleic anhydride grafted low density polyethylene (LDPE-g-MA) as a compatibilizer were prepared by melt mixing. LDPE-g-MA was prepared using a solution process. The maximum grafting degree was obtained at 6 wt% maleic anhydride (MA) and 0.2 wt% dicumyl peroxide (DCP) at 120 A degrees C and 240 min. Functional groups not found in pure LDPE were observed with the formation of LDPE-g-MA. The successful dispersion of CaCO3 particles in the HDPE matrix using LDPE-g-MA was revealed. The crystallite size of the composites was a little higher than that of CaCO3. The mechanical properties of the HDPE/CaCO3/LDPE-g-MA composites increased with decreasing CaCO3 content. Thermogravimetric analysis (TGA) revealed a higher thermal stability for the HDPE/CaCO3/LDPE-g-MA composites than for pure HDPE. Differential scanning calorimetry (DSC) revealed that the crystallization conditions were not substantially different. However, melting enthalpy and crystallinity increased with decreasing CaCO3 content. The thermal stability was greatly improved compared to that previously reported for nano CaCO3.
引用
收藏
页码:3258 / 3266
页数:9
相关论文
共 51 条
[1]   Chemical initiation mechanism of maleic anhydride grafted onto styrene-butadiene-styrene block copolymer [J].
Aimin, Z ;
Chao, L .
EUROPEAN POLYMER JOURNAL, 2003, 39 (06) :1291-1295
[2]   Fabrication and characterization of a novel hydrophobic CaCO3 grafted by hydroxylated poly(vinyl chloride) chains [J].
Bao, Lixia ;
Yang, Simei ;
Luo, Xin ;
Lei, Jingxin ;
Cao, Qiue ;
Wang, Jiliang .
APPLIED SURFACE SCIENCE, 2015, 357 :564-572
[3]   Toughness mechanism in semi-crystalline polymer blends: II. High-density polyethylene toughened with calcium carbonate filler particles [J].
Bartczak, Z ;
Argon, AS ;
Cohen, RE ;
Weinberg, M .
POLYMER, 1999, 40 (09) :2347-2365
[4]   Development of slate fiber reinforced high density polyethylene composites for injection molding [J].
Carbonell-Verdu, A. ;
Garcia-Garcia, D. ;
Jorda, A. ;
Samper, M. D. ;
Balart, R. .
COMPOSITES PART B-ENGINEERING, 2015, 69 :460-466
[5]   Nanoindentation and dynamic mechanical properties of PP/clay nanocomposites [J].
Chafidz, Achmad ;
Ali, Ilias ;
Mohsin, M. E. Ali ;
Elleithy, Rabeh ;
Al-Zahrani, Saeed .
JOURNAL OF POLYMER RESEARCH, 2012, 19 (07)
[6]   Atomic Force Microscopy, thermal, viscoelastic and mechanical properties of HDPE/CaCO3 nanocomposites [J].
Chafidz, Achmad ;
Ali, Ilias ;
Mohsin, M. E. Ali ;
Elleithy, Rabeh ;
Al-Zahrani, Saeed .
JOURNAL OF POLYMER RESEARCH, 2012, 19 (04)
[7]   Polypropylene/calcium carbonate nanocomposites [J].
Chan, CM ;
Wu, JS ;
Li, JX ;
Cheung, YK .
POLYMER, 2002, 43 (10) :2981-2992
[8]   Aqueous Foams Stabilized by in Situ Surface Activation of CaCO3 Nanoparticles via Adsorption of Anionic Surfactant [J].
Cui, Z-G. ;
Cui, Y-Z. ;
Cui, C-F. ;
Chen, Z. ;
Binks, B. P. .
LANGMUIR, 2010, 26 (15) :12567-12574
[9]   Development of biopolymer/cellulose/silica nanostructured hybrid materials and their characterization by NMR relaxometry [J].
dos Santos, Fernanda Abbate ;
Bruno Tavares, Maria Ines .
POLYMER TESTING, 2015, 47 :92-100
[10]  
Doufnoune R, 2003, INT J POLYM MATER, V52, P967, DOI DOI 10.1080/714975875