This research demonstrates a one-step modification process of biopolymer carrageenan active sites through functional group substitution in κ-carrageenan structures. The modification process improves the electronegative properties of κ-carrageenan derivatives, leading to enhancement of the material’s performance. Synthesized succinyl κ-carrageenan with a high degree of substitution provides more active sites for interaction with analytes. The FTIR analysis of succinyl κ-carrageenan showed the presence of new peaks at 1068 cm−1, 1218 cm−1, and 1626 cm−1 that corresponded to the vibrations of C–O and C=O from the carbonyl group. A new peak at 2.86 ppm in 1H NMR represented the methyl proton neighboring with C=O. The appearance of new peaks at 177.05 and 177.15 ppm in 13C NMR proves the substitution of the succinyl group in the κ-carrageenan structure. The elemental analysis was carried out to calculate the degree of substitution with the highest value of 1.78 at 24 h of reaction. The XRD diffractogram of derivatives exhibited a higher degree of crystallinity compared to pristine κ-carrageenan at 23.8% and 9.2%, respectively. Modification of κ-carrageenan with a succinyl group improved its interaction with ions and the conductivity of the salt solution compared to its pristine form. This work has a high potential to be applied in various applications such as sensors, drug delivery, and polymer electrolytes.
This research investigates the physicochemical properties of biopolymer succinyl-κ-carrageenan as a potential sensing material for NH4+ Localized Surface Plasmon Resonance (LSPR) sensor. Succinyl-κ-carrageenan was synthesised by reacting κ-carrageenan with succinic anhydride. FESEM analysis shows succinyl-κ-carrageenan has an even and featureless topology compared to its pristine form. Succinyl-κ-carrageenan was composited with silver nanoparticles (AgNP) as LSPR sensing material. AFM analysis shows that AgNP-Succinyl-κ-carrageenan was rougher than AgNP-Succinyl-κ-carrageenan, indicating an increase in density of electronegative atom from oxygen compared to pristine κ-carrageenan. The sensitivity of AgNP-Succinyl-κ-carrageenan LSPR is higher than AgNP-κ-carrageenan LSPR. The reported LOD and LOQ of AgNP-Succinyl-κ-carrageenan LSPR are 0.5964 and 2.7192 ppm, respectively. Thus, AgNP-Succinyl-κ-carrageenan LSPR has a higher performance than AgNP-κ-carrageenan LSPR, broader detection range than the conventional method and high selectivity toward NH4+. Interaction mechanism studies show the adsorption of NH4+ on κ-carrageenan and succinyl-κ-carrageenan were through multilayer and chemisorption process that follows Freundlich and pseudo-second-order kinetic model.
This paper demonstrates carbon quantum dots (CQDs) with triangular silver nanoparticles (AgNPs) as the sensing materials of localized surface plasmon resonance (LSPR) sensors for chlorophyll detection. The CQDs and AgNPs were prepared by a one-step hydrothermal process and a direct chemical reduction process, respectively. FTIR analysis shows that a CQD consists of NH2, OH, and COOH functional groups. The appearance of C=O and NH2 at 399.5 eV and 529.6 eV in XPS analysis indicates that functional groups are available for adsorption sites for chlorophyll interaction. A AgNP–CQD composite was coated on the glass slide surface using (3-aminopropyl) triethoxysilane (APTES) as a coupling agent and acted as the active sensing layer for chlorophyll detection. In LSPR sensing, the linear response detection for AgNP–CQD demonstrates R2 = 0.9581 and a sensitivity of 0.80 nm ppm−1, with a detection limit of 4.71 ppm ranging from 0.2 to 10.0 ppm. Meanwhile, a AgNP shows a linear response of R2 = 0.1541 and a sensitivity of 0.25 nm ppm−1, with the detection limit of 52.76 ppm upon exposure to chlorophyll. Based on these results, the AgNP–CQD composite shows a better linearity response and a higher sensitivity than bare AgNPs when exposed to chlorophyll, highlighting the potential of AgNP–CQD as a sensing material in this study.
Detection of nutrients in the hydroponics system, particularly nitrogen, phosphorus, and potassium (NPK) are critical to ensure the good production of crops. Currently, nutrients are analyzed using spectroscopy and electrochemical techniques, which are tedious and sophisticated. This study was conducted to develop a localized surface plasmon resonance (LSPR) fiber optic sensor technique to measure how much content of these nutrients should be added in the soil to increase crop fertility. The main objectives of this study are to study the LSPR fiber sensor technology on NPK in hydroponic systems, to create a fiber optic sensor technique for measuring NPK in hydroponic systems, and finally to characterize the performance of fiber optic sensors for measuring NPK in hydroponic systems. The utilization of the sensing materials, chitosan in this work is to improve the sensitivity feature of the sensor. Chitosan is coated on the surface of the tapered optical fiber prior to the LSPR NPK detection. The results of the absorption spectra will be visible at the end of the experiment where the obtained data are analyzed using SpectraSuite software. The results show that a good linearity was obtained when used AgNP/chitosan as the sensing material with the sensitivity of 0.041 nm ppm-1 in comparison to that of AgNP with the sensitivity of 0.039 nm ppm-1. A better limit of detection (LOD) and limit of quantification (LOQ) was also observed for AgNP/chitosan which are 35.61 ppm and 107.91 ppm, respectively. Meanwhile, AgNP exhibits LOD and LOQ of 106.16 ppm and 494.43 ppm, respectively. It is expected that this work will be a good contributor to the United Nations Sustainable Development Goals (UN SDG), No. 2: Zero Hunger.
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