“…The standard cooling scan shows the formation of equal amounts of α-and γ-polymorphism. The authors studied the SN behavior from 122 to 160 C. The relative amount of α-and γ-crystals was determined by WAXS. In the DSC heating scans, the lower temperature melting peak corresponds to the fusion of γ-crystals, whereas the high temperature peak corresponds to the fusion of α-crystals.…”
Section: Self-nucleation and Preferential Polymorphismmentioning
Self-nucleation (SN) is a special nucleation process triggered by selfseeds or self-nuclei that are generated in a given polymeric material by specific thermal protocols or by inducing chain orientation in the molten or partially molten state. SN increases the nucleation density of polymers by several orders of magnitude, producing significant modifications to their morphology and overall crystallization kinetics. In fact, SN can be used as a tool for investigating the overall isothermal crystallization kinetics of slow-crystallizing materials by accelerating the primary nucleation stage in a previous SN step. Additionally, SN can facilitate the formation of one particular crystalline phase in polymorphic materials. The SN behavior of a given polymer is influenced by its molecular weight, molecular topology, and chemical structure, among other intrinsic and extrinsic characteristics. This review paper focuses on the applications of DSC-based SN techniques to study the nucleation, crystallization, and morphology of different types of polymers, blends, copolymers, and nanocomposites.
“…The standard cooling scan shows the formation of equal amounts of α-and γ-polymorphism. The authors studied the SN behavior from 122 to 160 C. The relative amount of α-and γ-crystals was determined by WAXS. In the DSC heating scans, the lower temperature melting peak corresponds to the fusion of γ-crystals, whereas the high temperature peak corresponds to the fusion of α-crystals.…”
Section: Self-nucleation and Preferential Polymorphismmentioning
Self-nucleation (SN) is a special nucleation process triggered by selfseeds or self-nuclei that are generated in a given polymeric material by specific thermal protocols or by inducing chain orientation in the molten or partially molten state. SN increases the nucleation density of polymers by several orders of magnitude, producing significant modifications to their morphology and overall crystallization kinetics. In fact, SN can be used as a tool for investigating the overall isothermal crystallization kinetics of slow-crystallizing materials by accelerating the primary nucleation stage in a previous SN step. Additionally, SN can facilitate the formation of one particular crystalline phase in polymorphic materials. The SN behavior of a given polymer is influenced by its molecular weight, molecular topology, and chemical structure, among other intrinsic and extrinsic characteristics. This review paper focuses on the applications of DSC-based SN techniques to study the nucleation, crystallization, and morphology of different types of polymers, blends, copolymers, and nanocomposites.
“…The latter is also limiting their use as additives for high melting semi‐crystalline polymers 5. 1,3,5‐Benzenetrisamide derivatives represent an alternative class of nucleating agents avoiding the mentioned drawbacks and showing remarkable nucleation effects in i‐PP6–9 and poly(vinylidene fluoride) (PVDF) 10. Owing to their amide moieties, these compounds can establish intermolecular forces via hydrogen bonds resulting in one‐dimensional columnar self‐assemblies.…”
Section: Introductionmentioning
confidence: 99%
“…Herein we report on 1,3,5‐benzenetrisamides as supramolecular nucleating agents for PBT. To evaluate structurally different 1,3,5‐benzenetrisamides as potential nucleating agents, a screening method described by Abraham and Schmidt10 for PVDF was adapted for PBT. Promising compounds were investigated in a concentration range from 0.006 wt% (60 ppm) to 0.8 wt% (8000 ppm) and compared with respect to their dissolution and crystallization behavior of the additive in the PBT melt and the crystallization temperature of PBT.…”
1,3,5‐Benzenetrisamide‐based supramolecular nucleating agents for poly(butylene terephthalate) (PBT) are reported. 1,3,5‐Benzenetrisamides combine excellent thermal stability with chemical resistance, basic requirements for the use in high‐melting thermoplastics. To establish structure–property relationships, the central core and peripheral substituents are varied systematically. Dissolution and crystallization behavior of the additives in the PBT melt and the crystallization temperature of PBT are investigated as a function of the additive concentration. Efficient nucleating agents can increase the crystallization temperature of PBT by 10.6 °C to 199.1 °C. A visualization of supramolecular nano‐objects formed in the polymer melt is provided.
“…The synthesis and characterization were described in detail elsewhere [28e31]. They have been used as nucleation agents for iPP [24] and PVDF [32] and as supramolecular nanofibers [33,34]. As a reference alpha-nucleating agent, the commercially available nucleation agent, Irgaclear XT386 (alpha NA; supplier: BASF SE) and as a reference beta-nucleating agent (beta Ref), the commercially available nucleating agent, NJStar NU-100 (N,N-dicyclohexyl-2,6-naphthalene dicarboxamide, supplier: New Japan Chemical Co) were used as received.…”
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