Giant Cushioning Effect in Facile Polymer/Nanoclay-Coated Flexible Polyurethane Foams.

In this work, a flexible polyurethane (PU) foam/polymer/clay (PUF/PAASep) composite is prepared via a simple dip-coating method. The composite exhibits excellent damping properties under quasi-static compression, vibration transmissibility, and impact resistance. For the composite preparation, sepiolite (Sep) dispersion in a polyacrylic acid (PAA) solution is first homogenized and evaluated using microscopy, and the obtained PAASep suspension is used to coat the PU foam uniformly for optimization of the quasi-static mechanical performance of the foam composites.

Modified Sepiolite Nanoclays in Advanced Composites for Engineering Applications.

Clay-polymer nanocomposites (CPNs) containing a small weight fraction of nanoclay are known to display enhanced mechanical and thermal properties compared to neat polymers. However, the preparation and application of such nanocomposites remain challenging owing to the difficulties in dispersing nanoclays in polymer matrices. This study focuses on two surfactant-modified organophilic sepiolite clays to demonstrate the simplicity of the modification process, as well as on the use of a benzoxazine monomer (i.

Properties and Curing Kinetics of a Processable Binary Benzoxazine Blend.

A benzoxazine system is presented combining liquid cardanol-based benzoxazine (CA-a) and an effective initiator (3,3'-thiodipropionic acid, TDA) to bisphenol A-based benzoxazine (BA-a). The resultant mixture of monomeric precursors shows excellent fluidity and a relatively low peak polymerization temperature of around 200 °C. Moreover, the cured polybenzoxazine displays a high thermal decomposition temperature ( > 330 °C), a moderately high glass transition temperature (∼148 °C), and robust mechanical strength (storage modulus ∼ 2.

Controlling Kinetic Pathways in Demixing Microgel-Micelle Mixtures.

We investigate the temperature-dependent phase behavior of mixtures of poly(-isopropylacrylamide) (pNIPAM) microgel colloids and a triblock copolymer (PEO-PPO-PEO) surfactant. Usually, gelation in these systems results from an in temperature. Here we investigate the role of the heating rate, and surprisingly, we find that this causes the mechanism of aggregation to change from one which is driven by depletion of the microgels by the micelles at low temperatures to the association of the two species at high temperatures.

Oxidative degradation of triblock-copolymer surfactant and its effects on self-assembly.

We investigate the degradation behaviour of a triblock-copolymer surfactant made from polyethylene oxide (PEO) and polypropylene oxide (PPO) (PEO-PPO-PEO), highlighting how the aggregation behaviour of this polymer in water alters with ageing. Samples aged at room temperature were compared to samples degraded using accelerated ageing at elevated temperatures. We find that large mass losses occurred to the polymer surfactant which resulted in a change in the aggregation behaviour, with larger, rod-like or planar aggregates forming at longer degradation times.