Ternary-nanocomposites of polyamide 12 (PA-12) and multi-walled carbon nanotubes-embedded-polypropylene (MWCNT-embedded-PP) were fabricated by direct-melt-mixing-route and characterized for their dispersion-nanomorphology and phase-selective micromorphology. The crystallite sizes remained in the range of 8–9 nm and a broadening in loss-tangent peaks shifting towards higher temperatures with MWCNT was observed. The DC electrical conductivity remained dependent on the change in morphology from domain-dispersed (MWCNT-embedded-PP dispersed in PA-12 matrix) in PA-12/PP-MWCNT (70:30) to quasi-co-continuous (MWCNT-embedded-PP forming elongated domains of PP-MWCNT dispersed in PA-12 matrix tending to be near-continuous) in PA-12/PP-MWCNT (60:40). The conceptual feasibility of designing nanocomposites wherein the switch-over in solid-state relaxation behaviour vis-a-vis electrical conductivity is thus found to be controlled by morphology that ensures phase-selective conductive response for functional applications, as in flexible electronics, unlike the ones with rigid and high melting (thermally stiff) polyamides such as polyamide 6 or polyamide 66.

通过直接熔融混合法制备了聚酰胺12（PA-12）和多壁碳纳米管-嵌入聚丙烯（MWCNT-embedded-PP）的三元纳米复合材料，并对其分散-纳米形态和相选择微观形态进行了表征。 。微晶尺寸保持在8–9 nm范围内，并且观察到MWCNT的损耗角正切峰向更高的温度变宽。DC电导率仍然取决于形态的变化，从PA-12 / PP-MWCNT（70:30）中的畴分散（MWCNT嵌入的PP分散在PA-12基质中）到准准分子在PA-12 / PP-MWCNT中（60:40）的-co-连续（分散在PA-12基质中的PP-MWCNT的MWCNT嵌入PP形成的伸长域趋于接近连续）（60:40）。设计纳米复合材料的概念可行性，因此发现固态弛豫行为相对于电导率的转换受形态学控制，该形态学确保了功能性应用的相选择导电响应，例如在柔性电子学中，这与柔性电子学不同。含有硬质和高熔点（热硬性）聚酰胺的聚酰胺，例如聚酰胺6或聚酰胺66。