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Wearable textile colorimetric sensors are extremely effective for expressing danger or warning, as they are non‐invasive and exhibit easily recognizable color changes. However, unlike conventional sensors, these devices are actually worn by individuals and should, therefore, not only detect hazardous chemicals in real time but also maintain the reversibility, durability, and stability of color change upon exposure to sweat, repetitive movement, and environments involving continuous exposure to chemical substances. Herein, a halochromic fiber maintaining excellent pH sensing properties upon continuous exposure to chemical and physical stimuli is fabricated. The fiber surface is rendered hydrophobic by phosphonic acid treatment, and a composite pH indicator dye capable of simultaneously detecting acids and bases is embedded into the fiber pores. The halochromic fiber could accurately detect pH while maintaining a clear color transition even after repeated changes in the acidic–basic environment, returning to the neutral state within several seconds after termination of exposure to the test solution. Thus, the presented technique allows one to significantly improve the reversibility, durability, and stability of color change—a problem faced by conventional wearable sensors—and, thus, greatly contributes to the development of halochromic textile sensors applicable to real‐life work environments.
Wearable textile colorimetric sensors are extremely effective for expressing danger or warning, as they are non‐invasive and exhibit easily recognizable color changes. However, unlike conventional sensors, these devices are actually worn by individuals and should, therefore, not only detect hazardous chemicals in real time but also maintain the reversibility, durability, and stability of color change upon exposure to sweat, repetitive movement, and environments involving continuous exposure to chemical substances. Herein, a halochromic fiber maintaining excellent pH sensing properties upon continuous exposure to chemical and physical stimuli is fabricated. The fiber surface is rendered hydrophobic by phosphonic acid treatment, and a composite pH indicator dye capable of simultaneously detecting acids and bases is embedded into the fiber pores. The halochromic fiber could accurately detect pH while maintaining a clear color transition even after repeated changes in the acidic–basic environment, returning to the neutral state within several seconds after termination of exposure to the test solution. Thus, the presented technique allows one to significantly improve the reversibility, durability, and stability of color change—a problem faced by conventional wearable sensors—and, thus, greatly contributes to the development of halochromic textile sensors applicable to real‐life work environments.
The preparation of ethylenediaminetetraacetic acid (EDTA) functionalized pine needles biochar (EDTA@BC) as a low‐cost active adsorbent and its effectiveness in removing Ni(II) from aqueous solution at various conditions is reported in this paper. First, alkali activation was selected to render the pine needle biochar with an excellent porous structure and increased concentration of hydroxyl groups to facilitate grafting. Subsequently, a simple method was utilized to graft EDTA onto the biochar. The prepared EDTA@BC was characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and energy dispersive x‐ray spectrometry (EDX). Batch adsorption studies were conducted to assess the impact of various parameters such as solution pH, adsorbent dosage, adsorbate volume, and shaking time on the removal efficiency of Ni(II). At pH 6, 100 mg dosage, 4 mL of adsorbate volume, and 10 min of shaking time, the maximum removal efficiency of Ni(II) was observed to be 89%. EDTA@BC showed reasonable sorption performance still after the third cycle of regeneration. The effect of interfering ions such as Pb, Cr, Cu, and Hg was evaluated, resulting a decrease of 69%, 78%, 76%, and 68%, respectively, in its sorption capacity. The Langmuir model provided a better fit for Ni(II) in the concentration range of 0.1–2000 ppm under optimized conditions, with qmax of 46.69 ± 1.031 mg/g and KL of 0.001, compared with the Freundlich isotherm, which yielded n = 0.234 and χ2 = 2.7899, Temkin isotherm (R2 = 0.9520), and Redlich‐Peterson isotherm (R2 = 0.9725). The removal of Ni(II) by EDTA@BC was found to be the pseudo‐second‐order kinetics. Thermodynamic studies indicated adsorption process to be endothermic and nonspontaneous. Hence, a sustainable valorized bio‐material (EDTA@BC) is prepared having better sorption efficiency of Ni(II) from aqueous solution with possible wide applicability.Research Highlights New EDTA functionalized indigenous pine needles biochar (EDTA@BC) was prepared. This low‐cost active adsorbent found effective in removing Ni(II) from aqueous solution. FTIR, SEM, and EDX proved synthesis and uptake of Ni(II) from aqueous solution. Ni(II) removal, regeneration, interfering and adsorption studies were performed by UV–Vis spectroscopy.
A original electrochemical sensing platform, based on screen-printed electrodes modification with plasma polymerized acrylonitrile (pp-AN) nanofilms is proposed. For that purpose, plasma-enhanced chemical vapor deposition (PECVD) process was conducted in a parallel plate (13.56 MHz) plasma reactor for 2 min with discharge power of 10 W. The surface topography and electrochemical properties of prepared sensors were investigated by X-ray photoelectron spectroscopy, scanning electron microscopy, energy dispersion spectroscopy, electrochemical impedance spectroscopy, and cyclic voltammetry. The electrochemical characteristics of pp-AN/SPCE and pp-AN/SPAuE sensors was investigated for model redox pair [Fe(CN)6]4−/3−. Conducted research confirmed the excellent chemical stability, durability, wide potential window, high signal-to-noise (S/N) ratio, and, most importantly, the ability to standardize the sensors. The pp-AN/SPCE sensor was applied to the determination of bupropion, an antidepressant drug whose intake has increased dramatically during the COVID-19 pandemic. The voltammetric response of pp-AN/SPCE for BUP was linear in two concentration ranges of 0.63–10.0 and 10.0–50.0 μmol L−1, with a detection limit of 0.21 μmol L−1. Satisfactory recoveries (96.2–102%) and good precision (RSD below 4.1%) obtained for environmental and biological samples confirmed the usefulness of the sensor for the analysis of various kinds of samples. Graphical Abstract
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