Poly1-hexene: New impact modifier in HIPS technology

被引:28
作者
Hanifpour, Ahad [1 ]
Bahri-Laleh, Naeimeh [1 ]
Nekoomanesh-Haghighi, Mehdi [1 ]
Mirmohammadi, Seyed Amin [2 ]
机构
[1] IPPI, Polymerizat Engn Dept, POB 14965-115, Tehran, Iran
[2] Islamic Azad Univ, Dept Chem Engn, Tehran Cent Branch, Tehran, Iran
关键词
applications; elastomers; emulsion polymerization; polyolefins; RUBBER PARTICLE-SIZE; POLYSTYRENE HIPS; RADICAL POLYMERIZATION; MECHANICAL-PROPERTIES; PS/EPDM BLENDS; STYRENE; OZONOLYSIS; NANOCOMPOSITES; POLYBUTADIENE; POLYHEXENE-1;
D O I
10.1002/app.43882
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly1-hexene was prepared using a conventional heterogeneous Ziegler-Natta catalyst and its stereoregularity was characterized using C-13-NMR analysis. New kind of high impact polystyrene (HIPS) was prepared by radical polymerization of styrene in the presence of different amounts of synthesized poly1-hexene (PH) as impact modifier (HIPS/PH) and compared with conventional high impact polystyrene with polybutadiene (HIPS/PB) as rubber phase. Scanning electron microscopy (SEM) revealed that the dispersion of poly1-hexene in polystyrene matrix was more uniform compared with it in HIPS/PB. The impact strength of HIPS/PH was 29-79% and 80-289% higher than that in HIPS/PB and neat polystyrene, respectively. FTIR was used to confirm more durability of HIPS/PH samples toward ozonation. To study the effect of rubber type and amount on the T(g)s of polystyrene, differential scanning calorimetry was employed. Results obtained from TGA demonstrated higher thermal stability of HIPS/PH sample in comparison with conventional HIPS/PB one. Our obtained results suggest new high impact polystyrene that in all studied aspects has better performance than the conventional HIPS. (C) 2016 Wiley Periodicals, Inc.
引用
收藏
页数:8
相关论文
共 39 条
[21]   Preparation and characterization of thermally stable poly(amide-urea)s functionalized with anthraquinone chromophore [J].
Mehdipour-Ataei, Shahram ;
Bahri-Laleh, Naeemeh .
POLYMERS FOR ADVANCED TECHNOLOGIES, 2008, 19 (04) :291-298
[22]   Structure-property relationships of soluble poly(ester-urea)s containing naphthyl groups [J].
Mehdipour-Ataei, Shahram ;
Bahri-Laleh, Naeemeh ;
Rabei, Ahmad ;
Saidi, Samaneh .
HIGH PERFORMANCE POLYMERS, 2007, 19 (03) :283-295
[23]   Comparison of one-step and two-step methods of polyimidization and substitution effect in the synthesis of new poly(ester-imide)s with bulky pendent group [J].
Mehdipour-Ataei, Shahram ;
Bahri-Laleh, Naeemeh ;
Amirshaghaghi, Ahmad .
POLYMER DEGRADATION AND STABILITY, 2006, 91 (11) :2622-2631
[24]   Structure-property relations in heat resistant polyesters with built-in ether and imide units [J].
Mehdipour-Ataei, Shahram ;
Amirshaghaghi, Ahmad ;
Bahri, Naeemeh .
EUROPEAN POLYMER JOURNAL, 2006, 42 (10) :2646-2654
[25]   Continuous bulk process for the production of high-impact polystyrene: Recent developments in modeling and control [J].
Meira, Gregorio R. ;
Luciani, Carla V. ;
Estenoz, Diana A. .
MACROMOLECULAR REACTION ENGINEERING, 2007, 1 (01) :25-39
[26]   The effects of solvent and initiator on anionic ring opening polymerization of ε-caprolactone: synthesis and characterization [J].
Mirmohammadi, Seyed Amin ;
Imani, Mohammad ;
Uyama, Hiroshi ;
Atai, Mohammad ;
Teimouri, Mohammad Bagher ;
Bahri-Lale, Naeimeh .
POLYMER INTERNATIONAL, 2014, 63 (03) :479-485
[27]   Ozonolysis of unsaturated organotrifluoroborates [J].
Molander, Gary A. ;
Cooper, David J. .
JOURNAL OF ORGANIC CHEMISTRY, 2007, 72 (09) :3558-3560
[28]   Synthesis of highly isotactic poly 1-hexene using Fe-doped Mg(OEt)2/TiCl4/ED Ziegler-Natta catalytic system [J].
Nouri-Ahangarani, Farshid ;
Bahri-Laleh, Naeimeh ;
Nekoomanesh-Haghighi, Mehdi ;
Karbalaie, Milad .
DESIGNED MONOMERS AND POLYMERS, 2016, 19 (05) :394-405
[29]  
Pearce E.M., 1987, J POLYM SCI C, V25, P233, DOI DOI 10.1002/POL.1987.140250509
[30]   POLYBUTADIENE GRAFTING AND CROSS-LINKING IN HIGH-IMPACT POLYSTYRENE BULK THERMAL-PROCESS [J].
PENG, FM .
JOURNAL OF APPLIED POLYMER SCIENCE, 1990, 40 (7-8) :1289-1302