In this study, a versatile sensing platform based on a commercially available filter paper for the development of a colorimetric sensor using label-free gold nanoparticles (AuNPs) for the detection of cyanide in water is presented. The developed sensor can be applied for the direct detection of cyanide from an aqueous sample efficiently in a wide concentration range. The synthesised AuNPs were found to have an average size of about 13.2 ± 2.65 nm with a surface plasmon resonance peak at around 525 nm. Successful integration of AuNPs on the WFP substrate was observed through the FESEM-EDX analysis and supported by the presence of an absorbance peak at about 528 nm on the spectrum of the WFP-AuNPs composite. The colour of the WFP-AuNPs composite changed from purple-red to white in the presence of cyanide. Using the paper-based sensor, the limit of detection is calculated to be 7.68 × 10−6 M (0.5 ppm). The said sensitivity is good enough for the determination of cyanide in industrial wastewater samples. The developed sensor also showed excellent selectivity towards cyanide over other ions, demonstrating its practical applicability to monitor cyanide contamination in different environmental samples. Furthermore, the applicability of the sensor was demonstrated using several real water samples spiked with cyanide, including creek and tap water. Notably, the sensor showed great promise for the rapid, cost-effective, and versatile monitoring of cyanide contamination in various aqueous samples.

This work presents the synthesis of silver nanoparticles (AgNPs) capped with polyvinylpyrrolidone (PVP) via a simple chemical reduction approach. A route in controlling the optical absorbance of the AgNPs by varying the concentration of silver precursors, as reflected by the shifts and broadening of the UV-vis spectra of the AgNPs is also highlighted. Dynamic Light Scattering results revealed the narrow and small hydrodynamic size for AgNPs synthesized at low precursor concentration, while multiple hydrodynamic size peaks were observed for AgNPs produced at high precursor concentration. Likewise, Fourier transform-infrared spectroscopy confirmed the successful capping of PVP on the AgNPs through the O and N atoms as potential binding sites. Transmission electron micrographs revealed the formation of spherical PVP-capped AgNPs, having no apparent aggregation observed. A closer inspection of the micrograph showed the subsequent formation of rod-like growth template of the AgNPs, that might lead to the formation of non-spherical silver nanostructures.

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The rampant use of cyanide in mining activities has posed a substantial hazard to aquatic ecosystems and human health. Herein, a composite film of poly(vinyl alcohol)/chitosan (PVA/CS) with gold nanoparticles was synthesized as a potential colorimetric sensor for cyanide ions detection in water. The utilized AuNPs with a mean diameter of 14.32±3.49 nm were synthesized by chemical reduction using polyethyleneimine. Ultraviolet-visible spectroscopy revealed the characteristic peak of AuNPs at around 530 nm in the spectrum of PVA/CS/AuNP film, while SEM microscopy revealed the integration AuNPs across the polymer substrate. A color change from red to colorless was observed on the composite film after the addition of water samples with cyanide ions with a visual detection limit between 0.1-1 ppm. The sensor also exhibited good selectivity towards cyanide against the tested water samples containing

Copper contamination to water bodies is an environmental concern of significant risk due to its harmful effect on aquatic life forms and human beings. Herein, a paper-based colorimetric sensor was fabricated by immobilizing polyethyleneimine-capped silver nanoparticles (PEI-AgNPs) on commercial filter paper. The sensitivity and selectivity of the paper-based sensor's colorimetric response to copper ions in water were investigated. PEI-AgNPs with an average diameter of 12.66 ± 4.07 nm were successfully immobilized on the filter paper by the simple dipping technique, as evidenced by the scanning electron microscopy with energy-dispersive x-ray result. A color change from pale yellow to dark yellow green was noted after exposing the paper sensor in a water sample with copper ions. This colorimetric response was exclusively observed for copper ions only, suggesting the selectivity of the paper sensor towards copper ions. Moreover, ultraviolet-visible spectroscopy results revealed that the detection limit of the paper sensor was observed to about 1.0 ppm. Meanwhile, color analysis on the sensor's digital images revealed the linear response of the sensor with decreasing copper ion concentration down to 1.0 ppm. The selectivity of the sensor was also observed by the color intensity profile of the sensor. This work presents promising results that can be utilized as a reference for developing affordable, fast, portable, and reliable sensing devices for on-site water quality monitoring and other applications.