Relative quantification of long chain branching in essentially linear polyethylenes

被引:35
作者
Garcia-Franco, Cesar A. [4 ]
Lohse, David J. [1 ]
Robertson, Christopher G. [2 ]
Georjon, Olivier [3 ]
机构
[1] ExxonMobil Res & Engn Co, Corp Strateg Res, Annandale, NJ 08801 USA
[2] Bridgestone Amer, Ctr Res & Technol, Akron, OH 44317 USA
[3] ExxonMobil Chem Europe Inc, European Technol Ctr, B-1831 Hermeslaan, Belgium
[4] ExxonMobil Chem Co, Baytown Technol & Engn Complex, Baytown, TX 77522 USA
关键词
rheology; long chain branching; polyethylene; dynamic complex modulus; phase angle;
D O I
10.1016/j.eurpolymj.2007.10.030
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The aim of this work is to describe a method whereby low levels of long chain branching, LCB, can be quantified on a relative basis for whole, unfractionated, and essentially linear ethylene/alpha-olefin copolymers. The method is based on a well established, relatively fast and robust experiment, namely the measurement of the linear viscoelastic properties by a single, isothermal, small amplitude oscillatory shear experiment. The analysis of the data is predicated on the use of the so-called van Gurp-Palmen plots (the phase angle, delta(=tan(-1)(G ''/G')), plotted against the absolute value of the dynamic complex modulus, vertical bar G*vertical bar = (G'(2)+G ''(2))(1/2)). From this plot, the value of delta at vertical bar G*vertical bar = 10 kPa is recorded, and it is demonstrated that the amount of LCB inversely correlates with such value of the phase angle, delta. Depending on the desired frequency range, the experiment duration varies between 15 and 60 min rendering this technique well suited for high throughput parallel testing. Its applicability is critically examined with a wide variety of commercial ethylene/alpha-olefin copolymers. Moreover, we have improved on the long chain branching index (LCBI) proposed by Shroff and Mavridis [Shroff RN, Mavridis H. Long-chain-branching index for essentially linear polyethylenes. Macromolecules 1999;32:8454-64] by basing it on data of truly linear polyethylenes (hydrogenated anionically synthesized polybutadienes) instead of apparently linear commercial polyethylenes. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:376 / 391
页数:16
相关论文
共 33 条
  • [1] DISTRIBUTION OF MOLECULAR-WEIGHTS AND BRANCHING OF HIGH-DENSITY POLYETHYLENE
    AGARWAL, RK
    HORSKA, J
    STEJSKAL, J
    QUADRAT, O
    KRATOCHVIL, P
    HUDEC, P
    [J]. JOURNAL OF APPLIED POLYMER SCIENCE, 1983, 28 (11) : 3453 - 3466
  • [2] [Anonymous], MACROMOL
  • [3] PREDICTION OF RHEOLOGICAL BEHAVIOR OF BRANCHED POLYETHYLENE FROM MOLECULAR-STRUCTURE
    BERSTED, BH
    SLEE, JD
    RICHTER, CA
    [J]. JOURNAL OF APPLIED POLYMER SCIENCE, 1981, 26 (03) : 1001 - 1014
  • [4] RELAXATION OF ENTANGLED POLYMERS IN MELTS
    DESCLOIZEAUX, J
    [J]. MACROMOLECULES, 1990, 23 (17) : 3992 - 4006
  • [5] DESCLOIZEAUX J, 1988, EUROPHYS LETT, V5, P437
  • [6] Doi M., 1986, The Theory of Polymer Dynamics
  • [7] Packing length influence in linear polymer melts on the entanglement, critical, and reptation molecular weights
    Fetters, LJ
    Lohse, DJ
    Milner, ST
    Graessley, WW
    [J]. MACROMOLECULES, 1999, 32 (20) : 6847 - 6851
  • [8] CONNECTION BETWEEN POLYMER MOLECULAR-WEIGHT, DENSITY, CHAIN DIMENSIONS, AND MELT VISCOELASTIC PROPERTIES
    FETTERS, LJ
    LOHSE, DJ
    RICHTER, D
    WITTEN, TA
    ZIRKEL, A
    [J]. MACROMOLECULES, 1994, 27 (17) : 4639 - 4647
  • [9] Prediction of melt state poly(α-olefin) rheological properties:: The unsuspected role of the average molecular weight per backbone bond
    Fetters, LJ
    Lohse, DJ
    García-Franco, CA
    Brant, P
    Richter, D
    [J]. MACROMOLECULES, 2002, 35 (27) : 10096 - 10101
  • [10] Fetters LJ, 1999, J POLYM SCI POL PHYS, V37, P1023, DOI 10.1002/(SICI)1099-0488(19990515)37:10<1023::AID-POLB7>3.0.CO