Modification of the mechanical properties of polyamide 6 multifilaments in high-speed melt spinning with nano silicates

被引:19
作者
Steinmann, Wilhelm [1 ]
Walter, Stephan [1 ]
Gries, Thomas [1 ]
Seide, Gunnar [1 ]
Roth, Georg [2 ]
机构
[1] RWTH Aachen Univ ITA, Inst Text Tech, D-52074 Aachen, Germany
[2] RWTH Aachen Univ XTAL, Inst Kristallog, Aachen, Germany
关键词
melt spinning; multifilament yarn; nanocomposites; polyamide; 6; structure analysis; CRYSTALLIZATION BEHAVIOR; TEMPERATURE-DEPENDENCE; CRYSTAL STRUCTURE; NYLON-6; NANOCOMPOSITES; ORIENTATION; POLYMER; GAMMA; TRANSFORMATION; POLYMORPHISM;
D O I
10.1177/0040517512456756
中图分类号
TB3 [工程材料学]; TS1 [纺织工业、染整工业];
学科分类号
0805 ; 080502 ; 0821 ;
摘要
In the last few years research activities have been focused on the modification of fiber properties with nano-scaled additives. One of the most important fields of research is the alteration of mechanical properties such as the tenacity and the specific breaking load. In this study, we determined the influence of nano-phyllosilicates on the drawability of polyamide 6 multifilament yarns. It was first demonstrated that the drawability of the fibers drastically increased in an industrially relevant high-speed melt spinning process. Structural properties of the material are identified by wide-angle X-ray diffraction (WAXD) and differential scanning calorimetry (DSC). Changes in the crystalline properties as well as in the alignment of the silicates are compared with the stress-strain curves of the fibers, and a molecular mechanism for the drawing process is derived from these experiments. In a first step, a significant phase transition in the crystalline structure unaffected by the silicates occurs for low draw ratios (DRs). Beyond this point, where unmodified fibers start to break, a gliding between the silicate layers takes place, which is responsible for an extended drawability of the fibers. This mechanism leads to new possibilities for fiber processing, which can be used to research ultra-fine filaments in future studies.
引用
收藏
页码:1846 / 1858
页数:13
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