A novel series of composites of polyarylene ether nitrile terminated with phthalonitrile (PEN-t-Ph) filled with hybrid Fe3O4 nanospheres (h-Fe 3 O 4 ) was prepared via in situ composition. Based on the cross-linking interactions between the phthalonitrile at the end of PEN-t-Ph molecular chains and the phthalonitrile on the surface of h-Fe 3 O 4 particles to form phthalocyanine ring, it was shown that the PEN-t-Ph/h-Fe 3 O 4 system had superior interfacial compatibility and the h-Fe 3 O 4 particles were locked in the matrix resin. These results had been confirmed by scanning electron microscope analysis. By orthogonal experiments and statistic analysis, the optimal conditions of cure temperature, type of h-Fe 3 O 4 and content of h-Fe 3 O 4 had been determined. Meanwhile, the results of range analysis and variance analysis indicated that the cure temperature had great effects on the thermal properties. Thermal studies revealed that the glass transition temperature of PEN-t-Ph/h-Fe 3 O 4 cured at 320 C was 214.
Fresh foods are vulnerable to foodborne pathogens which cause foodborne illness and endanger people's life and safety. The rapid detection of foodborne pathogens is crucial for food safety surveillance. An in situ-synthesized gene chip for the detection of foodborne pathogens on fresh-cut fruits and vegetables was developed. The target genes were identified and screened by comparing the specific sequences of Salmonella Typhimurium, Vibrio parahemolyticus, Staphylococcus aureus, Listeria monocytogenes, and Escherichia coli O157:H7 from the National Center for Biotechnology Information database. Tiling array probes were designed to target selected genes in an optimized hybridization system. A total of 141 specific probes were selected from 3,227 hybridization probes, comprising 26 L. monocytogenes, 24 S. aureus, 25 E. coli O157:H7, 20 Salmonella Typhimurium, and 46 V. parahemolyticus probes that are unique to this study. The optimized assay had strong amplification signals and high accuracy. The detection limit for the five target pathogens on fresh-cut cantaloupe and lettuce was approximately 3 log cfu/g without culturing and with a detection time of 24 h. The detection technology established in this study can rapidly detect and monitor the foodborne pathogens on fresh-cut fruits and vegetables throughout the logistical distribution chain, i.e., processing, cleaning, fresh-cutting, packaging, storage, transport, and sale, and represents a valuable technology that support the safety of fresh agricultural products.
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