A sensitive paper-based vapor-test kit for instant formalin detection in food products.

A colorimetric sensing method based on a paper-based vapor-test kit was successfully developed for the selective and sensitive real-time monitoring of formalin in food samples. The device was specifically designed to efficiently extract and detect formalin simultaneously. A microcentrifuge tube was used as the sample solution container, with the inner cap serving as the reaction and detection zone. Formalin was converted into gaseous formaldehyde through controlled heating, which was then extracted and collected on a filter paper coated with Nash's reagent. The color change on paper was used for formalin quantification using a smartphone for detection and image analysis. Under optimal conditions, our method provided a linear range of 0.5-75 mg L-1 with a detection limit of 0.11 mg L-1. This method effectively determined formalin in fresh food and vegetable samples, with recoveries ranging from 92 to 111%, demonstrating comparable accuracy to the standard method for practical food quality control and safety.

Eco-Friendly Starch Composite Supramolecular Alginate-Ca2+ Hydrogel as Controlled-Release P Fertilizer with Low Responsiveness to Multiple Environmental Stimuli.

Environmentally friendly fertilizers (EFFs) have been developed to improve fertilizer efficiency and minimize adverse environmental impacts, but their release behavior under various environmental conditions has been less explored. Using phosphorus (P) in the form of phosphate as a model nutrient, we present a simple method for preparing EFFs based on incorporating the nutrient into polysaccharide supramolecular hydrogels using Cassava starch in the Ca2+-induced cross-link gelation of alginate. The optimal conditions for creating these starch-regulated phosphate hydrogel beads (s-PHBs) were determined, and their release characteristics were initially evaluated in deionized water and then under various environmental stimuli, including pH, temperature, ionic strength, and water hardness. We found that incorporating a starch composite in s-PHBs at pH = 5 resulted in a rough but rigid surface and improved their physical and thermal stability, compared with phosphate hydrogel beads without starch (PHBs), due to the dense hydrogen bonding-supramolecular networks. Additionally, the s-PHBs showed controlled phosphate-release kinetics, following a parabolic diffusion with reduced initial burst effects. Importantly, the developed s-PHBs exhibited a promising low responsiveness to environmental stimuli for phosphate release even under extreme conditions and when tested in rice field water samples, suggesting their potential as a universally effective option for large-scale agricultural activities and potential value for commercial production.

Enhanced adsorption and colorimetric detection of tetracycline antibiotics by using functional phosphate/carbonate composite with nanoporous network coverage.

This work presents efficient tetracycline (TC) antibiotics adsorption using a functional porous phosphate/carbonate composite (PCC). The PCC was fabricated by anion-exchange of phosphate on the surface of vaterite-phase calcium carbonate particle scaffolds. The PCC, having dense nanoporous network coverage with large surface area and pore volume, exhibited excellent TC adsorption in solution. Its adsorption isotherm fitted well to the Freundlich model, with a maximum adsorption capacity of 118.72 mg/g. The adsorption process was spontaneous, endothermic, and followed pseudo-second-order kinetics. From the XPS analysis, the hydrogen bonding and surface complexation were the key interactions in the process. In addition, a colorimetric TC detection method was developed considering its complexation with phosphate ions, originating from PCC dissolution, during adsorption. The method was used to detect TC in mg/L concentrations in water samples. Thus, the multifunctional PCC exhibited potential for use in TC removal and environmental remediation.

Fabrication of Porous Phosphate/Carbonate Composites: Smart Fertilizer with Bimodal Controlled-Release Kinetics and Glyphosate Adsorption Ability.

A simple method to prepare phosphate/carbonate composites for use as porous sponge-like phosphate fertilizers (ps-PO4Fs) is presented. The composites ps-PO4Fs were prepared by ion-exchange implantation of phosphate onto the surface of vaterite-phase calcium carbonate (CaCO3) microparticles. The ps-PO4Fs obtained under the optimized conditions were found to contain a nanoscale porous network of calcium phosphate covering the CaCO3 support. In addition, ps-PO4Fs exhibited two distinct phosphate release modes having different kinetics: a fast-release step over the initial 24 h period following a parabolic diffusion model, indicating controlled diffusion from external surfaces/edges, and a second slow-release step over the course of a month following the Ritger-Peppas model, indicating the release and diffusion of phosphate adsorbed at specific sites. The ps-PO4Fs also adsorbed glyphosate well because of their porous structure and large surface area. However, glyphosate adsorption prevented phosphate release at concentrations greater than 10 mg L-1. The ps-PO4Fs were tested for their effects on plant growth and showed effects similar to commercial fertilizers. In summary, these smart, eco-friendly, and multifunctional fertilizers having two-stage phosphate release could enable the application of lower amounts of fertilizer and remove excess glyphosate from the environment.

A rapid and simple method for the removal of dyes and organophosphorus pesticides from water and soil samples using deep eutectic solvent embedded sponge.

A new treatment method using a deep eutectic solvent embedded melamine sponge (DES-MS) was studied for the removal of organic pollutants from water and soil samples. Five organophosphorus pesticides (OPPs) consisting of azinphos-methyl (AZP), parathion-methyl (PRT), fenitrothion (FNT), diazinon (DIZ) and chlorpyrifos (CPF), and two dyes including acid blue 29 (AB29) and malachite green (MG) were used as the model pollutants. DESs were easily prepared from tetrabutylammonium bromide (TBABr) and various fatty acids. The synthesised DESs were loaded into the sponge before being utilized for the removal of the studied pollutants. After the removal, the residual OPPs or dyes in the supernatant was quantified by high performance liquid chromatography or derivative spectrophotometry, respectively. The proposed method was simple, rapid, environmentally friendly and effective with the removal efficiency higher than 70% for various samples. Moreover, the removal of various dyes was successfully achieved with the efficiency greater than 65% under the optimum condition.

An instrument-free method based on visible chemical waves for quantifying the ethanol content in alcoholic beverages.

An alternative approach using visible chemical waves for ethanol determination is presented. The method is based on the dynamic change of chemical waves in the Belousov-Zhabotinsky (BZ) reaction by perturbation with ethanol. The observablepropagating waves, generatedina Petri dish, can be recorded by using a smartphone camera. The propagating distances are measured from photographic images and then plotted as a function of time to attain the wave velocity. It is found that wave velocities are inversely proportional to ethanol concentrations. By using this linear relationship, the ethanol content can be efficiently quantified with good intra-day and inter-day precision (<3% RSD). Validated by the GC technique, the developed method is highly reliable and successfully applied for quantifying the ethanol content in beer, colored whisky, and vodka samples. Hence, this new method provides an alternative practical strategy for simple quantitative detection of ethanol without the need for instruments.

The use of dissolvable layered double hydroxide components in an in situ solid-phase extraction for chromatographic determination of tetracyclines in water and milk samples.

This research presents a simple and green in situ solid phase extraction (is-SPE) combined with high-performance liquid chromatography (HPLC) for the simultaneous analysis of tetracyclines (TCs) including tetracycline, oxytetracycline, and chlortetracycline. In is-SPE, TCs were efficiently extracted through the precipitation formation of dissolvable layered double hydroxides (LDHs) by mixing the LDH components such as magnesium and aluminum ions (both in metal chloride salts) thoroughly in an alkaline sample solution. After the centrifugation, the precipitate was completely dissolved with trifluoroacetic acid to release the enriched TCs, and then analyzed by HPLC. Under optimized conditions, this method gave good enrichment factors (EFs) of 41-93 with low limits of detection (LODs) of 0.7-6µg/L and limits of quantitation (LOQs) of 3-15µg/L. Also, the proposed method was successfully applied for the determination of TCs in water and milk samples with the recoveries ranging from 81.7-108.1% for water and 55.7-88.7% for milk.

The alternative use of layered double hydroxides as extraction medium coupled with microcomplexation for determination of phosphate in water samples.

A simple, rapid, in situ, and green extraction combined with a microcomplexation has been developed for the spectrophotometric determination of phosphate in water samples. Through their formation, layered double hydroxides (LDHs) were employed as the extraction medium, instantly commenced by a rapid addition of a mixed solution of Mg2+ and Al3+ ions into alkaline phosphate solution. After the extraction, LDH precipitate containing phosphate was dissolved by sulfuric acid and the released phosphate was subsequently detected via its complexation with molybdate in the presence of antimonyl and ascorbic acid. Under optimum conditions, the linearity in the range of 5-200µgL-1, with the correlation coefficient (r2) of 0.9969, and the enrichment factor (EF) of 14 were obtained. The limit of detection (LOD) of 5µgL-1 and good precision, with the relative standard deviations (RSDs) less than 8.16%, were achieved. The proposed method was successfully applied to determine phosphate in water samples and the relative recoveries of 72.97-115.32% were obtained.

A New Approach for Removing Anionic Organic Dyes from Wastewater Based on Electrostatically Driven Assembly.

A conceptually new approach for an efficient removal of anionic organic dyes from wastewater using layered double hydroxides (LDHs) through their formation is presented. Acid yellow 25 (AY25) was used as anionic organic dye model molecules. As a result of the electrostatic induction, the removal mechanism involved a concurrent incorporation of AY25 molecules into the interlayer of LDHs during their structural arrangement, where Mg(2+) and Al(3+) ions were utilized to construct the base of LDHs in an alkaline solution. It was found that the molar stoichiometry of all precursors was a key factor affecting the removal efficiency. Within 5 min removal time, this method still maintained high removal efficiency of over 97% and provided a removal capacity of ∼186 mg g(-1), comparable to that of other LDH-based methods. Also, almost complete dye recovery was simply achieved by anionic exchange with common anions (Cl(-), NO3(-), and CO3(2-)). Additionally, the present technique is straightforward, cost-effective, and environmentally friendly since it avoids the synthesis step of sorbents, thus significantly saving time, chemicals, and energy. Hence, this strategy not only exhibits the alternative exploitation of LDHs, but also provides new insights into the removal of contaminants from wastewater.