RESUMEN
Cotton gin waste presents a significant challenge in the cotton ginning industry due to its abundant generation and limited disposal options. In this study, we explored the potential of cotton gin waste as a naturally occurring source material that can synthesize and host silver nanoparticles. The noncellulosic constituents of cotton gin waste served as effective reducing agents, facilitating the conversion of silver ions into silver atoms, while its porous structure acted as a microreactor, enabling controlled particle growth. A simple heat treatment of cotton gin waste powder in an aqueous silver precursor solution actualized the in situ synthesis of silver nanoparticles, without the need for additional chemical agents. Remarkably, a high concentration of silver nanoparticles (14.7%) with an average diameter of approximately 27 nm was produced throughout the entire volume of cotton gin waste. Electron microscopic images of cross-sectioned cotton gin waste confirm the internal formation of nanoparticles. Rietveld refinement analysis of X-ray diffraction patterns showed that the majority of the nanoparticles possess a cubic silver crystal structure. By leveraging the well-known biocidal properties of silver nanoparticles, the resulting silver nanoparticle-filled cotton gin waste holds promise for novel antimicrobial and antifungal material applications.
RESUMEN
Luminescent oligomers and polymers doped with silver(I) salts were used as optical sensors for ethylene and other gaseous small molecules. Films of poly(vinylphenylketone) (PVPK) or 1,4-bis(methylstyryl)benzene (BMSB) impregnated with AgBF(4), AgSbF(6), or AgB(C(6)F(5))(4) respond to ethylene exposures with a reversible emission quenching that is proportional to the pressure of the gas. Experiments with various analytes revealed that only gases capable of forming coordinate bonds with Ag(I) ions (i.e., ethylene, propylene, and ammonia) produced a sensing response. Comparison of the effects of ethylene and tetradeuterioethylene revealed that the emission quenching was due to enhanced vibrational relaxation. The Ag(I) ions are essential to the observed optical response. The oligomer/polymer support enhances the response characteristics of the impregnated salt by promoting separation of Ag(I) from its anion, a separation that improves accessibility of the Ag(I) ion to the gaseous analytes. Salts with large lattice energies, where the anion is not dissociated from Ag(I) in the matrix, fail to sensitize film responses. Photoluminescence experiments with Ag(I)-impregnated BMSB films established that the Ag(I) ions serve to communicate the analyte-binding signal to the support by altering the support-based emission. These experiments demonstrate a sensing paradigm where simultaneous coordination of Ag(I) ions to the support matrix and to a gaseous analyte enables the optical response.