Effect of catalyst residues on the chain structure and properties of a Phillips type polyethylene

被引:23
作者
Epacher, E
Kröhnke, C
Pukánszky, B
机构
[1] Hungarian Acad Sci, Inst Chem, Chem Res Ctr, H-1525 Budapest, Hungary
[2] Clariant Huningue SA, Polymer Additives, F-68331 Huningue, France
[3] Tech Univ Budapest, Dept Plast & Rubber Technol, H-1521 Budapest, Hungary
关键词
D O I
10.1002/pen.11275
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A large number of high-density polyethylene (HDPE) po cc der samples produced by Phillips technology were taken from an industrial polymerization reactor and their catalyst residue content was determined by X-ray fluorescence spectroscopy. The chemical structure of the powder was characterized by diffuse reflectance infrared spectroscopy (DRIFT), while the functional group content of samples processed in the presence and absence of a phenolic antioxidant was determined by Fourier transform infrared spectroscopy (FTIR). The melt flow index (MFI) of all processed samples was measured. Oxygen induction time (OIT) measurements were carried out to characterize the oxidative stability of 15 selected stabilized samples. The results indicate that the distribution of both the amount of chromium-based catalyst residues and their composition are very heterogeneous in the produced polymer. With increasing catalyst residue content, the concentration of double bonds increases in the samples extruded with or without stabilizer. Viscosity was not influenced by catalyst residues, while discoloration increased slightly with increasing catalyst residue content. The stability of the processed polymer also depends on the concentration of double bonds and on other factors. Since other components of the catalyst, including the SiO2 support, also take part in the reactions occurring during processing, chromium content is not the sole, and perhaps not even the decisive, factor determining the properties and especially the stability of HDPE produced by a Phillips catalyst.
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页码:1458 / 1468
页数:11
相关论文
共 84 条
[1]   LIGHT STABILIZER, ANTIOXIDANT AND PIGMENT INTERACTIONS IN THE THERMAL AND PHOTOCHEMICAL OXIDATION OF POLYETHYLENE FILMS [J].
ALLEN, NS ;
VASILIOU, C ;
MARSHALL, GP ;
CHEN, W .
POLYMER DEGRADATION AND STABILITY, 1989, 24 (01) :17-31
[2]   INFRARED SPECTROMETRIC DETERMINATION OF CATALYSTS USED IN THE PRODUCTION OF HIGH-DENSITY POLYETHYLENE [J].
BATTISTE, DR ;
BUTLER, JP ;
CROSS, JB ;
MCDANIEL, MP .
ANALYTICAL CHEMISTRY, 1981, 53 (14) :2232-2234
[3]  
Beach D. L., 1986, ENCY POLYM SCI ENG, V6, P454
[4]   INFLUENCE OF REACTOR CONDITIONS, ANTIOXIDANT, AND PROCESSING ON THE DEGRADATION OF LDPE [J].
BERGSTROM, C ;
BRENNER, J ;
STENIUS, P .
JOURNAL OF APPLIED POLYMER SCIENCE, 1979, 23 (12) :3563-3573
[5]   CATALYST CHARACTERIZATION - VARIATION OF SEVERAL PARAMETERS WITH THE DEACTIVATION REGENERATION CYCLES [J].
BRITO, A ;
BORGES, ME ;
ARVELO, R ;
GARCIA, T .
APPLIED CATALYSIS A-GENERAL, 1993, 103 (01) :17-21
[6]   PREPARATION AND CHARACTERIZATION OF BIMETALLIC OXIDES OF CHROMIUM AND TITANIUM [J].
CHENG, S ;
CHENG, SY .
JOURNAL OF CATALYSIS, 1990, 122 (01) :1-9
[7]   SYNERGISM OF ANTIOXIDANTS IN HIGH-DENSITY POLYETHYLENE [J].
CHIRINOSPADRON, AJ ;
HERNANDEZ, PH ;
ALLEN, NS ;
VASILION, C ;
MARSHALL, GP ;
DEPOORTERE, M .
POLYMER DEGRADATION AND STABILITY, 1987, 19 (02) :177-189
[8]  
CHOI KY, 1985, J MACROMOL SCI R M C, VC25, P1
[9]  
CONVAY SJ, 1989, J CHEM SOC F1, V85, P71
[10]  
DESLAURIERS PJ, 1995, ANTEC, V41, P3639