Crystallisation behaviour of high density polyethylene blends with bimodal molar mass distribution

2004 ◽  
Vol 40 (2) ◽  
pp. 371-378 ◽  
Author(s):  
Andres Krumme ◽  
Arja Lehtinen ◽  
Anti Viikna
e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Yujing Tang ◽  
Zhiyong Jiang ◽  
Jens Rieger ◽  
Hans-Friedrich Enderle ◽  
Dieter Lilge ◽  
...  

AbstractThe isothermal crystallization behavior of two different high density polyethylene grades with monomodal and bimodal molar mass distribution was investigated by means of differential scanning calorimetry. The results indicate that extensive cocrystallization between linear short chains and long chains with short branches in bimodal polyethylene grade occurred. In contrast, polymer chains of different lengths in monomodal polyethylene exhibit different tendency to crystallize. This finding was explained qualitatively based on a general discussion of the effect of molar mass and branch content/length on crystallization tendency of polymeric chains.


1989 ◽  
Vol 54 (7) ◽  
pp. 1821-1829
Author(s):  
Bedřich Porsch ◽  
Simon King ◽  
Lars-Olof Sundelöf

The differences between the QELSS and classical diffusion coefficient of a polydisperse polymer resulting from distinct definitions of experimentally accessible average values are calculated for two assumed specific forms of molar mass distributions. Predicted deviations are compared with the experiment using NBS 706 standard polystyrene. QELSS Dz of this sample relates within 2-4% to the classical diffusion coefficient, if the Schulz-Zimm molar mass distribution is assumed to be valid. In general, differences between the height-area and QELSS diffusion coefficient of about 20% may be found for Mw/Mn ~ 2, and this value may increase above 35%, if strongly tailing molar mass distribution pertains to the sample.


2012 ◽  
Vol 293 (3) ◽  
pp. 941-947 ◽  
Author(s):  
E. Elshereafy ◽  
Maysa A. Mohamed ◽  
M. M. EL-Zayat ◽  
A. A. El Miligy

2019 ◽  
Vol 89 (23-24) ◽  
pp. 5067-5075 ◽  
Author(s):  
Helena Wedin ◽  
Marta Lopes ◽  
Herbert Sixta ◽  
Michael Hummel

The aim of this study is to improve the understanding of which end-of-life cellulosic textiles can be used for chemical recycling according to their composition, wear life and laundering—domestic versus service sector. For that purpose, end-of-life textiles were generated through laboratorial laundering of virgin fabrics under domestic and industrial conditions, and the cellulose content and its intrinsic viscosity and molar mass distribution were measured in all samples after two, 10, 20, and 50 laundering cycles. Results presented herein also address the knowledge gap concerning polymer properties of end-of-life man-made cellulosic fabrics—viscose and Lyocell. The results show that post-consumer textiles from the home consumer sector, using domestic laundering, can be assumed to have a similar, or only slightly lower, degree of polymerization than the virgin textiles (−15%). Post-consumer textiles from the service sector, using industrial laundering, can be assumed to have a substantially lower degree of polymerization. An approximate decrease of up to 80% of the original degree of polymerization can be expected when they are worn out. A higher relative decrease for cotton than man-made cellulosic textiles is expected. Furthermore, in these laboratorial laundering trials, no evidence evolved that the cellulose content in blended polyester fabrics would be significantly affected by domestic or industrial laundering. With respect to molar mass distribution, domestic post-consumer cotton waste seems to be the most suitable feedstock for chemical textile recycling using Lyocell-type processes, although a pre-treatment step might be required to remove contaminants and lower the intrinsic viscosity to 400–500 ml/g.


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