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This study explored the combined influence of shear flow and nucleating agents on isotactic polypropylene (iPP) crystallisation. The study showed that oriented a-iPP crystals were not necessary to form b-iPP crystals, contrary to the accepted view that the surface of oriented a-iPP crystals provides nucleation sites for an a-iPP to b-iPP growth transition. Instead it was proposed that flow-induced mesomorphic point-like nuclei preferentially nucleates b-iPP. The combined effect of shear flow and nucleant was found to promote g-iPP crystals. The surprising g-iPP nucleation effect was explained by the high density of flow-induced and heterogeneous nuclei present at the start of crystallisation.

The present study presents a method to predict the flow distribution imposed on an injection moulded melt crystallised isotactic polypropylene (iPP) from its experimentally determined morphological distribution. A microrheological model, based on the Doi–Edwards model, was used to calculate the flow-induced free energy for the flow-induced crystallisation. The low limit flow field required to generate the final structures was then obtained. The effect of Cu-phthalocyanine (CuPc), a nucleating agent, on the flow history was also studied. Instead of geometric positions, structural parameters such as molecular orientation and crystallinity were correlated to the flow history of the injection-moulded iPP. The work provides a simple approach to predict flow–structure relationships for complex thermo-mechanical processing treatments, which can then guide the realistic design and control of the flow-induced crystallisation of polymers.

The morphology of isotactic polystyrene (iPS) particles which had been compounded into an isotactic polypropylene (iPP) matrix was varied in-situ by selective heat treatment to be either amorphous (iPS amorphous ) or semicrystalline (iPS crystalline ). The influence of iPS morphology on the quiescent and shear-induced isothermal crystallisation of iPP was then studied using differential scanning calorimetry (DSC), in-situ simultaneous small and wide angle X-ray scattering (SAXS/WAXS) and polarised optical microscopy (POM). In the quiescent condition iPS crystalline was found to selectively nucleate the β phase while iPS amorphous nucleated the α phase of iPP. Compared to the control sample (iPP control ), the presence of both morphologies of iPS increased the number of shear-induced oriented crystal precursors that form as a result of the step shear. During isothermal crystallisation the shear-induced nuclei promote oriented α form crystal growth, accelerate the crystallisation kinetics and ultimately swamp the effect of the nucleating particles present.

Francisella noatunensis subsp. orientalis (Fno) is the causative agent of piscine francisellosis in warm water fish including tilapia. The disease induces chronic granulomatous inflammation with high morbidity and can result in high mortality. Early and accurate detection of Fno is crucial to set appropriate outbreak control measures in tilapia farms. Laboratory detection of Fno mainly depends on bacterial culture and molecular techniques. Recombinase polymerase amplification (RPA) is a novel isothermal technology that has been widely used for the molecular diagnosis of various infectious diseases. In this study, a recombinase polymerase amplification (RPA) assay for rapid detection of Fno was developed and validated. The RPA reaction was performed at a constant temperature of 42 degreesC for 20 min. The RPA assay was performed using a quantitative plasmid standard containing a unique Fno gene sequence. Validation of the assay was performed not only by using DNA from Fno, closely related Francisella species and other common bacterial pathogens in tilapia farms, but also by screening 78 Nile tilapia and 5 water samples. All results were compared with those obtained by previously established real-time qPCR. The developed RPA showed high specificity in detection of Fno with no cross-detection of either the closely related Francisella spp. or the other tested bacteria. The Fno-RPA performance was highly comparable to the published qPCR with detection limits at 15 and 11 DNA molecules detected, respectively. The RPA gave quicker results in approximately 6 min in contrast to the qPCR that needed about 90 min to reach the same detection limit, taking only 2.7- 3 min to determine Fno in clinical samples. Moreover, RPA was more tolerant to reaction inhibitors than qPCR when tested with field samples. The fast reaction, simplicity, cost-effectiveness, sensitivity and specificity make the RPA an attractive diagnostic 41 tool that will contribute to controlling the infection through prompt on-site detection of Fno.