Starch-derived carbon quantum dots: Unveiling structural insights and photocatalytic potential as a bio-sourced metal-free semiconductor.

The optical appeal and sustainability of carbon quantum dots (CQDs) have led to these nanoparticles swiftly gaining attention and emerging as a new, multifunctional class of nanomaterials. This work centers on the hydrothermal preparation of CQDs utilizing starch, an abundant and renewable biopolymer, as the precursor. Extensive characterization via spectroscopy and microscopy techniques revealed that the starch-derived CQDs exhibit a spherical nanoscale morphology averaging a âˆ¼ 4 nm diameter, demonstrating a red-orange photoluminescence emission. Diffuse reflectance spectroscopic analysis verified their semiconductor behavior, with an estimated direct band gap of 4.1 eV comparable to conventional semiconductors. The prepared CQDs demonstrated considerable promise as metal-free, semiconductor photocatalysts for degrading aqueous dye pollutants under UV irradiation. High photodegradation efficiencies of 45.11 %, 62.94 %, and 91.21 % were achieved for Acid Blue 21, Reactive Blue 94, and Reactive TB 133 dyes, respectively. Systematic investigations of critical process parameters like pH, CQDs dosage, dye concentration, and contact time provided vital insights into the photocatalytic mechanism. The bio-sourced CQD nanomaterials offer a sustainable pathway for effective environmental remediation.

Nitrogen and sulfur dual doped porous carbon as metal-free catalyst for oxidative degradation of 4-nitrophenol by persulfate activation.

The replacement of metals in catalytic processes is highly demanded to improve sustainability and economic growth. Poor stability and metal leaching are the main drawbacks of metal-based catalytic reactions. This work represented the use of nitrogen and sulfur-co-doped mesoporous carbon material ((N, S)-MPC) as a metal-free catalyst for the degradation of 4-nitrophenol (4-NP) as a priority pollutant announced by the Environmental Protection Agency through the persulfate-based advanced oxidation process. A low amount of (N, S)-MPC catalyst (0.3 g/L) exhibited superior performance for the degradation of 4-NP within 3 h at room temperature and unadjusted pH. The COD removal was calculated to be 76% using (N, S)-MPC catalyst. Interestingly, the degradations kinetics of 4-NP followed the zero-order kinetics with the rate constant of 0.505 min-1. The radical quenching experiment was accomplished to investigate the activation pathway of degradation. A real sample from an oil and gas company was treated with the (N, S)-MPC catalyst, which showed excellent total decontamination of 61%. The recyclability and stability of the catalyst have been evaluated for three runs. Owing to the obvious benefits such as high efficiency, metal-free nature, and recyclability, the presented catalyst can improve pollutant removal from aqueous media and practical environmental remediation.

Correction: Gold nanoparticles supported on supramolecular ionic liquid grafted graphene: a bifunctional catalyst for the selective aerobic oxidation of alcohols.

[This corrects the article DOI: 10.1039/C3RA44696D.].

Forward osmosis dewatering of seawater and pesticide contaminated effluents using the commercial fertilizers and zinc-nitrate blend draw solutions.

Fertilizer driven forward osmosis (FDFO) process would be feasible due to the possible prevention of the drainage of dewatered and concentrated pesticide effluent from agricultural pesticide industries to the environment. Instead, it would be possible to return the concentrated pesticide solution to the processing cycle, and on the other hand, employ directly the obtained diluted fertilizer draw solution for irrigation. This study investigated the performance of zinc-nitrate/amino-acids blends as fertilizer type draw solution, and distilled water, saline water (seawater), and synthetic wastewater containing pesticides as feed. The results indicated that the synergetic effect of blended type fertilizer presented significantly higher osmotic pressure and water flux than the sum of their individual ones, especially when the amount of amino acid increased. Conversely, an ignorable reverse flux of blended fertilizer draw solute was observed. The fertilizer blend with a molar ratio of 1:6 zinc-nitrate/amino-acid achieved the higher average fluxes of 34.7 and 23.92 L/m2h from distilled and saline waters compared to common draw solutions such as metal salts. Furthermore, the FDFO exhibited a high rejection (over 99%) of bentazon and imidacloprid in feed solutions compared to other agricultural pesticides due to their larger molecular weight and molecular size. The applied FDFO represented a significant reduction in specific energy consumption (from 0.17 to 0.049 kWh/m3) in a bench-scale setup as compared to the RO process almost at the same water permeation flux and the rejection of bentazon.

Structural investigation and application of Tween 80-choline chloride self-assemblies as osmotic agent for water desalination.

Forward osmosis (FO) process has been extensively considered as a potential technology that could minimize the problems of traditional water desalination processes. Finding an appropriate osmotic agent is an important concern in the FO process. For the first time, a nonionic surfactant-based draw solution was introduced using self-assemblies of Tween 80 and choline chloride. The addition of choline chloride to Tween 80 led to micelles formation with an average diameter of 11.03 nm. The 1H NMR spectra exhibited that all groups of Tween 80 were interacted with choline chloride by hydrogen bond and Van der Waals' force. The influence of adding choline chloride to Tween 80 and the micellization on its osmotic activity was investigated. Despite the less activity of single components, the average water flux of 14.29 L m‒2 h‒1 was obtained using 0.15 M of Tween 80-choline chloride self-assembly as draw solution in the FO process with DI water feed solution. Moreover, various concentrations of NaCl aqueous solutions were examined as feed solution. This report proposed a possible preparation of nonionic surfactant-based draw solutions using choline chloride additive with enhanced osmotic activities that can establish an innovative field of study in water desalination by the FO process.

Preconcentration and extraction of lead ions in vegetable and water samples by N-doped carbon quantum dot conjugated with Fe3O4 as a green and facial adsorbent.

Magnetically N-doped Carbon quantum dots has been synthesized via a simple chemical method and applied as a sorbent for the preconcentration and extraction of trace amounts of Pb2+ from water and vegetable samples followed by flame atomic absorption spectrometric detection. The nanoparticles were characterized by X-ray diffraction, UV-vis spectra, Fourier transform infrared spectroscopy, vibrating sample magnetometer analysis and transmission electron microscopy. A central-composite design was used to find the optimum conditions for the preconcentration procedure through response surface methodology. The effects of various parameters such as the pH value, adsorption time, amount of adsorbent, desorption conditions (type, concentration and volume of the eluent and desorption time), sample volume and interfering ions have been studied. Under the optimized conditions, the calibration graph was linear in the range of 0.3-300µgL-1 (R2=9992). The detection limit and pre-concentration factor were found to be 0.082µgL-1 and 265, respectively.

Highly selective determination of amitriptyline using Nafion-AuNPs@branched polyethyleneimine-derived carbon hollow spheres in pharmaceutical drugs and biological fluids.

In this paper, AuNPs@Polyethyleneimine-derived carbon hollow spheres were synthesized by a versatile and facile method in three steps and successfully developed and validated as Amitriptyline sensor using cyclic voltammetry (CV), chronoamperometry (CA) and differential pulse voltammetry (DPV) methods. The characterization of the electrode surface has been carried out by means of scanning electron microscopy (SEM), transmission electron microscopy (TEM), x-ray diffraction (XRD), x-ray photo-electron spectrum (XPS), electrochemical impedance spectroscopy (EIS) and chronocoulometry (CC). The obtained negatively charged modified electrode was highly selective to Amitriptyline and it was shown a wide linear range from 0.1 to 700µmolL(-1), with a lower detection limit of 0.034µmolL(-1) (n=5, S/N=3), revealing the high-sensitivity properties. The modified electrode is used to achieve the real-time quantitative detection of AMT for biological applications, and satisfactory results are obtained. Due to the advantages of the sensor, its selectivity, sensitivity and stability, it will have a bright future in the field of medical diagnosis.

Application of pH-sensitive magnetic nanoparticles microgel as a sorbent for the preconcentration of phenoxy acid herbicides in water samples.

Introducing new sorbents is an interesting and debatable issue in the field of sample preparation. In this study, for the first time, a pH-sensitive magnetic nanoparticles microgel, Fe3O4-SiO2-oly(4-vinylpyridine), was introduced as a new sorbent. The operating mechanism of this sorbent is based on changing the pH value of the sample and consequently the structure of this pH-sensitive microgel is changed. So that, at pH 6.0 the microgel was ready to accept and load the analytes (partial swelling), and when the pH was increased to 8.0, the microgel was closed and analytes were trapped inside the sorbent (deswelling). At pH 2.0 the microgel was opened and the analytes were released from the microgel (swelling). As the adsorption and desorption mechanism is based on changing the pH and only aqueous medium is used as the effluent solvent, this method is introduced as a green extraction method. The use of this microgel resulted in excellent figures of merit. The limits of quantitation and detection for herbicides were obtained within the range of 10-30 and 3-10 ng mL(-1), respectively. Finally, the proposed method was successfully applied to determine the concentration of phenoxy acid herbicides as hazardous materials in water samples.

The use of tetragonal star-like polyaniline nanostructures for efficient solid phase extraction and trace detection of Pb(II) and Cu(II) in agricultural products, sea foods, and water samples.

Due to importance of trace analysis of lead and copper ions because of their toxicity, in this paper, for the first time a unique tetragonal star-like morphology of polyaniline was applied as a efficient solid phase for selective trace separation of copper and lead at optimum experimental conditions in shrimp, fish and water samples. Due to the unique star like nanostructure of synthesized sorbent, the tendency of the sorbent toward selective extraction of lead and copper ion in the optimised pH is very interesting. The prepared polymeric resin displayed good figures of merits with analytical calibration curve ranging from 1 to 120 µg L(-1) for copper and 2 to 100 µg L(-1) for lead ions with limits of detection of 0.4 µg L(-1) for copper and 0.9 µg L(-1) for lead, adsorption capacities of 84 and 110 mg g(-1) for copper and lead ions, respectively, extraction efficiency of greater than 96%, and relative standard deviation (RSD) of less than 4% for eight separate column experiments in determination of 5.0 µg of lead and copper. The obtained data for adsorption capacity of the sorbent shows the high tendency of the sorbent toward the mentioned ions in this nanostructure form. Finally, this sorbent can be used as a simple, rapid, reliable, selective and sensitive method for determination of trace levels of Cu(II) and Pb(II).