Abstract

Polystyrene foams have become more and more important owing to their lightweight potential and their insulation properties. Progress in this field is expected to be realized by foams featuring a microcellular morphology. However, large-scale processing of low-density foams with a closed-cell structure and volume expansion ratio of larger than 10, exhibiting a homogenous morphology with a mean cell size of approximately 10 µm, remains challenging. Here, we report on a series of 4,4′-diphenylmethane substituted bisamides, which we refer to as kinked bisamides, acting as efficient supramolecular foam cell nucleating agents for polystyrene. Self-assembly experiments from solution showed that these bisamides form supramolecular fibrillary or ribbon-like nanoobjects. These kinked bisamides can be dissolved at elevated temperatures in a large concentration range, forming dispersed nano-objects upon cooling. Batch foaming experiments using 1.0 wt.% of a selected kinked bisamide revealed that the mean cell size can be as low as 3.5 µm. To demonstrate the applicability of kinked bisamides in a high-throughput continuous foam process, we performed foam extrusion. Using 0.5 wt.% of a kinked bisamide yielded polymer foams with a foam density of 71 kg/m3 and a homogeneous microcellular morphology with cell sizes of ≈10 µm, which is two orders of magnitude lower compared to the neat polystyrene reference foam with a comparable foam density.

Highlights

  • IntroductionUsing BTAs at large concentrations in lar polymers remains challenging due to restrictions in the solubility and the co tion-dependent formation of larger sized objects

  • We demonstrated that the class of kinked bisamides, based on various 4,40 -diphenylmethane central units and via amide-linked peripheral side groups, is highly suitable to act as efficient supramolecular foam cell nucleating agents for PS

  • Structural elucidation on a selected kinked bisamide reveals that such an elongated fibrillary or ribbon-like shape is attributed to the formation of two strands of hydrogen bonds, which can be regarded as the main driving force for a preferred one-dimensional crystal growth

Read more

Summary

Introduction

Using BTAs at large concentrations in lar polymers remains challenging due to restrictions in the solubility and the co tion-dependent formation of larger sized objects This probably limits the number dispersed nano-objects in the polymer melt under conventionally employed co and restricts a very large number of nucleation sites necessary for a fin blowing agent, this allows for control over the foam morphology with a homogeneous polymer fine cellularfoam. A novel class of supramolecular polymer additives, which were on cell nu and their nano-object morphology as well as their capability to act based as foam a 4,40 -diaminodiphenylmethane central unit with two side groups linked via two amide agents for polystyrene.

Materials
Self-Assembly of Kinked Bisamides and Nano-Object Characterization
Structural Studies of Kinked Bisamide 3a
Masterbatch Preparation
Compounding and Preparation of Injection-Molded Specimen for Batch Foaming
Batch Foaming
Extrusion Foaming
Foam Morphology
Foam Density
Cell Density
Results and Discussion
Self-Assembly of Kinked Bisamides from Xylene
Batch Foaming ofToPolystyrene
Extrusion Foaming of Polystyrene Using Kinked Bisamides
Conclusions
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call