On the rheological footprint of branching of polyethylene
عنوان مقاله: On the rheological footprint of branching of polyethylene
شناسه ملی مقاله: ISPST10_202
منتشر شده در دهمین سمینار بین المللی علوم و تکنولوژی پلیمر در سال 1391
شناسه ملی مقاله: ISPST10_202
منتشر شده در دهمین سمینار بین المللی علوم و تکنولوژی پلیمر در سال 1391
مشخصات نویسندگان مقاله:
Florian J. Stadler - School of Semiconductor and Chemical Engineering, Chonbuk National University, Baekjero 567, Deokjin-gu, Jeonju, Jeonbuk,561-756, Republic of Korea.
خلاصه مقاله:
Florian J. Stadler - School of Semiconductor and Chemical Engineering, Chonbuk National University, Baekjero 567, Deokjin-gu, Jeonju, Jeonbuk,561-756, Republic of Korea.
Two types of branching are relevant in polyethylene: shortand long-chain branches (SCB and LCB, respectively), whose distinction is defined by the entanglement molar mass Me.While SCB have a very distinct effect on the crystal structure and, thus, on the solid state and thermodynamic behaviour ofpolyethylenes (which will not be discussed in detail), LCBs significantly influence the melt-state properties – the rheological properties. The effect of long-chain branching onrheological properties is very distinct in both linear and nonlinear regime. Classically, one of the main ways to detect long-chainbranching is the correlation between zero shear-rate viscosity 0 and weight-average molar mass Mw, which for linearpolymers scales with approximately 3.4, while deviations sensitive to LCB-topography are found for LCB-PE. for low and medium branching levels, higher zero shear-rate viscosityby a factor 0/ 0 lin up to 100000 is found, while a high level of long-chain branching leads to a decrease of 0/ 0lin to down to 10-6 (Fig. 1) Although it would be logical, SCBs do not lead to a significant deviation from the 0-Mw-relation up tosignificant SCB-levels.1-3
صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/579571/