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• SERS revealed reorientation and packing density of BG with respect to the AgNP surface as a function of its concentration. • The presence of the cationic surfactant CTAB improved the SERS enhancement of BG. • Micelles create the optimum distances for the generation of "hotspots". • The presence of CTAB at CMC created the optimum distances between AgNPs for appropriate SERS active "hotspots". • SERRS has been applied to detect BG below its maximum allowable discharge concentration from ClearBal in marine water. Surface-enhanced Raman scattering (SERS) has been applied utilizing colloidal suspensions of silver nanoparticles (AgNPs), for the detection of brilliant green (BG) at very low concentrations. Proper stimulated surface-enhanced resonance Raman scattering (SERRS) spectra collected from BG aqueous solutions at different low concentration ranges revealed a variation of the relative intensity ratio of certain BG bands attributed to a respective alteration of the molecular orientation of the analyte with respect to the AgNPs. This behavior is closely related to a different packing of the BG molecules on the nanoparticle surface when the concentration increases and the available space decreases. Additionally, the addition of suitable amounts of cetyl thrimethyl ammonium bromide (CTAB) to the BG aqueous solutions enhanced the detection limit of the analyte. This enlightens the role of the cationic surfactant in tuning the interparticle distances of AgNPs in the colloidal suspension; this presumably allows an optimization of the SERS enhancement factor. The concentration of CTAB that maximizes the SERS of BG is the same with the critical micelle concentration (CMC) of the surfactant. Most probably, CTAB at the CMC acts as a spacer keeping the AgNPs at a certain distance suitable for the generation of SE(R)RS hotspots. [ABSTRACT FROM AUTHOR]

Hybrid polymeric materials incorporating carbon nanostructures or inorganic constituents stand as a promising class of materials exhibiting distinct but also complementary features. Carbon nanotubes have been proposed as unique candidates for polymer reinforcement; however, sustained efforts are further needed in order to make full use of their potential. The final properties of the reinforced polymer are controlled in part by the morphology and the eventual molecular orientation of the polymer matrix. In the present study, multiwall carbon nanotubes (MWCNTs) were utilized in order to reinforce polyethylene terephthalate (PET) composites. The effect of CNTs on the crystallization and the orientation of the structurally hybridized polymeric material has been investigated from the perspective of assessing their impact on the final properties of a relevant nanocomposite product. Functionalized MWCNTs were used to achieve their optimal dispersion in the polymer matrix. The physical properties of the composites (i.e., crystallinity and orientation) were characterized via differential scanning calorimetry, X-ray diffraction, and polarized Raman microscopy. The addition of well-dispersed CNTs acted as a nucleation agent, increasing the crystallization of the polyethylene terephthalate matrix and differentiating the orientation of both CNTs and macromolecular chains. [ABSTRACT FROM AUTHOR]